[{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140424945,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140424945,"source":"dbSNP","seq_region_name":"7","id":"rs2130170485","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140424950,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140424950,"clinical_significance":[],"id":"rs1799636923","seq_region_name":"7"},{"source":"dbSNP","start":140424955,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140424955,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1051810366"},{"feature_type":"variation","strand":1,"alleles":["G","C","T"],"end":140424956,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140424956,"clinical_significance":[],"seq_region_name":"7","id":"rs1274061753"},{"clinical_significance":[],"seq_region_name":"7","id":"rs890543095","end":140424961,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140424961,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1238879510","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140424962,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140424962},{"id":"rs1799637190","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140424963,"strand":1,"feature_type":"variation","start":140424963,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1184168640","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140424965,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140424965},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140424967,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140424967,"seq_region_name":"7","id":"rs947276396","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1250145265","source":"dbSNP","start":140424968,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140424968,"alleles":["T","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs943545537","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140424969,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140424969,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799637402","clinical_significance":[],"alleles":["A","T"],"end":140424971,"strand":1,"feature_type":"variation","start":140424971,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140424972,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140424972,"source":"dbSNP","seq_region_name":"7","id":"rs1189554867","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140424977,"source":"dbSNP","strand":1,"feature_type":"variation","end":140424977,"alleles":["A","T"],"id":"rs1799637557","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","C"],"end":140424981,"strand":1,"feature_type":"variation","start":140424981,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799637603","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1490953668","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140424982,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140424982},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140424984,"source":"dbSNP","strand":1,"feature_type":"variation","end":140424984,"alleles":["C","T"],"seq_region_name":"7","id":"rs1799637711","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130170680","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140424985,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140424985},{"start":140424993,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140424993,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799637772","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140425006,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425006,"source":"dbSNP","seq_region_name":"7","id":"rs1043091587","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425007,"source":"dbSNP","strand":1,"feature_type":"variation","end":140425007,"alleles":["C","T"],"seq_region_name":"7","id":"rs1266853153","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140425010,"alleles":["G","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425010,"clinical_significance":[],"seq_region_name":"7","id":"rs1799637941"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1419736229","source":"dbSNP","start":140425012,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140425012,"feature_type":"variation","strand":1},{"start":140425018,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140425018,"strand":1,"feature_type":"variation","id":"rs1799638064","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585435869","source":"dbSNP","start":140425019,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140425019,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140425023,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140425023,"alleles":["T","A","C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs7793448"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1240639948","feature_type":"variation","strand":1,"end":140425024,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425024},{"clinical_significance":[],"seq_region_name":"7","id":"rs10244642","end":140425026,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140425026,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425029,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140425029,"seq_region_name":"7","id":"rs2130170832","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1000423119","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140425031,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425031},{"alleles":["C","A"],"end":140425033,"strand":1,"feature_type":"variation","start":140425033,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1327816620","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799638707","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425035,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140425035},{"seq_region_name":"7","id":"rs560494758","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140425039,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425039,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1351271617","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425043,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140425043},{"id":"rs1799638868","seq_region_name":"7","clinical_significance":[],"start":140425056,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140425056,"alleles":["T","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1456127023","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425060,"feature_type":"variation","strand":1,"end":140425060,"alleles":["C","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425072,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140425072,"clinical_significance":[],"seq_region_name":"7","id":"rs891420708"},{"seq_region_name":"7","id":"rs1292569669","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425076,"source":"dbSNP","strand":1,"feature_type":"variation","end":140425076,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs1373488764","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425079,"source":"dbSNP","strand":1,"feature_type":"variation","end":140425079,"alleles":["A","G","T"]},{"seq_region_name":"7","id":"rs1585435942","clinical_significance":[],"start":140425081,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140425081,"alleles":["T","G"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140425085,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140425085,"alleles":["A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs879484504","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1585435958","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140425087,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425087,"source":"dbSNP"},{"source":"dbSNP","start":140425088,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140425088,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs191931046"},{"source":"dbSNP","start":140425092,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140425092,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799639417"},{"source":"dbSNP","start":140425102,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140425102,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1363403498","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1199886971","clinical_significance":[],"start":140425104,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140425104,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140425106,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425106,"clinical_significance":[],"seq_region_name":"7","id":"rs764555740"},{"strand":1,"feature_type":"variation","end":140425110,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425110,"source":"dbSNP","id":"rs1585435982","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425112,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140425112,"clinical_significance":[],"seq_region_name":"7","id":"rs1267222810"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130171091","feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140425113,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425113},{"clinical_significance":[],"id":"rs969768269","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140425116,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425116},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425117,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140425117,"clinical_significance":[],"seq_region_name":"7","id":"rs1222304301"},{"seq_region_name":"7","id":"rs1349741315","clinical_significance":[],"start":140425119,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140425119,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1023551274","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425124,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140425124},{"id":"rs1799639985","seq_region_name":"7","clinical_significance":[],"end":140425125,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140425125,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425129,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140425129,"seq_region_name":"7","id":"rs185235585","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799640102","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425131,"source":"dbSNP","strand":1,"feature_type":"variation","end":140425131,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799640152","end":140425138,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140425138,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140425140,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425140,"clinical_significance":[],"seq_region_name":"7","id":"rs1347962885"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425144,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140425144,"clinical_significance":[],"seq_region_name":"7","id":"rs974047972"},{"source":"dbSNP","start":140425146,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140425146,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs771974082"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425147,"feature_type":"variation","strand":1,"end":140425147,"alleles":["G","A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs370968609"},{"id":"rs1026662453","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140425149,"strand":1,"feature_type":"variation","start":140425149,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140425150,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425150,"source":"dbSNP","seq_region_name":"7","id":"rs962965129","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425155,"feature_type":"variation","strand":1,"end":140425155,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799640548"},{"seq_region_name":"7","id":"rs1799640603","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425171,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140425171},{"clinical_significance":[],"id":"rs1404169584","seq_region_name":"7","feature_type":"variation","strand":1,"end":140425173,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425173},{"end":140425175,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140425175,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs972642953","seq_region_name":"7"},{"start":140425176,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140425176,"strand":1,"feature_type":"variation","id":"rs2130171312","seq_region_name":"7","clinical_significance":[]},{"id":"rs1320248780","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140425178,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425178,"source":"dbSNP"},{"end":140425179,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140425179,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs190121010"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425180,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140425180,"clinical_significance":[],"seq_region_name":"7","id":"rs1799640903"},{"seq_region_name":"7","id":"rs1799640945","clinical_significance":[],"start":140425181,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140425181,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799640996","source":"dbSNP","start":140425183,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140425183,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1398980428","clinical_significance":[],"alleles":["T","C"],"end":140425184,"strand":1,"feature_type":"variation","start":140425184,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["C","T"],"end":140425185,"feature_type":"variation","strand":1,"source":"dbSNP","start":140425185,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799641094"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425189,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140425189,"seq_region_name":"7","id":"rs1799641147","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140425193,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425193,"clinical_significance":[],"seq_region_name":"7","id":"rs866041183"},{"source":"dbSNP","start":140425194,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140425194,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs950735623"},{"seq_region_name":"7","id":"rs912350859","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140425196,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425196,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425200,"source":"dbSNP","strand":1,"feature_type":"variation","end":140425200,"alleles":["C","T"],"seq_region_name":"7","id":"rs1799641369","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425201,"feature_type":"variation","strand":1,"end":140425201,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs987461980"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425208,"source":"dbSNP","strand":1,"feature_type":"variation","end":140425208,"alleles":["C","A","G"],"seq_region_name":"7","id":"rs73482582","clinical_significance":[]},{"end":140425209,"alleles":["CC","C"],"strand":1,"feature_type":"variation","start":140425208,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1199127124","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","C"],"end":140425210,"feature_type":"variation","strand":1,"source":"dbSNP","start":140425210,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1244296757"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1191693863","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425211,"feature_type":"variation","strand":1,"alleles":["GGG","GG"],"end":140425213},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425221,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140425221,"seq_region_name":"7","id":"rs1799641676","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140425222,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425222,"clinical_significance":[],"seq_region_name":"7","id":"rs760401018"},{"feature_type":"variation","strand":1,"end":140425228,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425228,"clinical_significance":[],"seq_region_name":"7","id":"rs1282944792"},{"seq_region_name":"7","id":"rs1203824894","clinical_significance":[],"start":140425232,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140425232,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425239,"source":"dbSNP","strand":1,"feature_type":"variation","end":140425239,"alleles":["C","T"],"id":"rs1799642086","seq_region_name":"7","clinical_significance":[]},{"end":140425242,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140425242,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799642130"},{"clinical_significance":[],"id":"rs1325226137","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425248,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140425248},{"clinical_significance":[],"id":"rs182291412","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425250,"feature_type":"variation","strand":1,"end":140425250,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1189100569","end":140425252,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140425252,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140425257,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140425257,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1416482353","clinical_significance":[]},{"source":"dbSNP","start":140425261,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140425261,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1362432230"},{"seq_region_name":"7","id":"rs1422412165","clinical_significance":[],"start":140425262,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140425262,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1799642483","clinical_significance":[],"start":140425264,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140425264,"strand":1,"feature_type":"variation"},{"start":140425267,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140425267,"strand":1,"feature_type":"variation","id":"rs1039622849","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","A"],"end":140425273,"strand":1,"feature_type":"variation","start":140425273,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1799642581","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799642632","clinical_significance":[],"strand":1,"feature_type":"variation","end":140425274,"alleles":["A","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425274,"source":"dbSNP"},{"seq_region_name":"7","id":"rs2130171686","clinical_significance":[],"alleles":["G","A"],"end":140425275,"strand":1,"feature_type":"variation","start":140425275,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs768429421","seq_region_name":"7","clinical_significance":[],"start":140425278,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140425278,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1799642735","seq_region_name":"7","feature_type":"variation","strand":1,"end":140425288,"alleles":["AAA","AAAAAAAA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425286},{"start":140425286,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AAACAAAACAAAACAAAACAAAACAAA","AAACAAAACAAAACAAA","AAACAAAACAAAACAAAACAAA","AAACAAAACAAAACAAAACAAAACAAAACAAA","AAACAAAACAAAACAAAACAAAACAAAACAAAACAAA","AAACAAAACAAAACAAAACAAAACAAAACAAAACAAAACAAA"],"end":140425312,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs540341868","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130171767","clinical_significance":[],"start":140425289,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140425289,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1410834724","clinical_significance":[],"alleles":["AAAA","AAAAAA"],"end":140425293,"strand":1,"feature_type":"variation","start":140425290,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140425293,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425293,"source":"dbSNP","seq_region_name":"7","id":"rs1799643003","clinical_significance":[]},{"end":140425294,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140425294,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130171802"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1422114545","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425302,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140425302},{"end":140425307,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140425307,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1166594135"},{"clinical_significance":[],"seq_region_name":"7","id":"rs926106567","source":"dbSNP","start":140425309,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140425309,"alleles":["C","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1799643200","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425314,"source":"dbSNP","strand":1,"feature_type":"variation","end":140425314,"alleles":["T","G"]},{"end":140425318,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140425318,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799643235","clinical_significance":[]},{"id":"rs936251217","seq_region_name":"7","clinical_significance":[],"start":140425320,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","G","T"],"end":140425320,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140425321,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140425321,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1238615072"},{"end":140425324,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140425324,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs947338202","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799643441","clinical_significance":[],"start":140425326,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140425326,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"end":140425328,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140425328,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130171904","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425329,"source":"dbSNP","strand":1,"feature_type":"variation","end":140425329,"alleles":["C","T"],"seq_region_name":"7","id":"rs1462296473","clinical_significance":[]},{"id":"rs1799643536","seq_region_name":"7","clinical_significance":[],"start":140425340,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140425340,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"alleles":["A","G"],"end":140425341,"feature_type":"variation","strand":1,"source":"dbSNP","start":140425341,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799643588","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425344,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140425344,"clinical_significance":[],"seq_region_name":"7","id":"rs1042930894"},{"seq_region_name":"7","id":"rs1799643698","clinical_significance":[],"start":140425347,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140425347,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"alleles":["T","C"],"end":140425350,"feature_type":"variation","strand":1,"source":"dbSNP","start":140425350,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799643743"},{"seq_region_name":"7","id":"rs1202662355","clinical_significance":[],"start":140425353,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140425353,"alleles":["C","G","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1307798744","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425354,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140425354},{"strand":1,"feature_type":"variation","end":140425355,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425355,"source":"dbSNP","seq_region_name":"7","id":"rs368888142","clinical_significance":[]},{"id":"rs1354710307","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","-"],"end":140425355,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425355,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799644034","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425358,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140425358},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425366,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140425366,"clinical_significance":[],"seq_region_name":"7","id":"rs924618836"},{"seq_region_name":"7","id":"rs1305576717","clinical_significance":[],"end":140425369,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140425369,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140425371,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140425371,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs934626951","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799644294","feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140425373,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425373},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425374,"feature_type":"variation","strand":1,"end":140425374,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1057051301"},{"seq_region_name":"7","id":"rs892038250","clinical_significance":[],"end":140425375,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140425375,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1013906432","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425376,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140425376},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425378,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140425378,"seq_region_name":"7","id":"rs1799644515","clinical_significance":[]},{"alleles":["C","T"],"end":140425382,"strand":1,"feature_type":"variation","start":140425382,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1045355891","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140425384,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425384,"clinical_significance":[],"seq_region_name":"7","id":"rs1799644620"},{"seq_region_name":"7","id":"rs895939993","clinical_significance":[],"strand":1,"feature_type":"variation","end":140425388,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425388,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799645268","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425389,"source":"dbSNP","strand":1,"feature_type":"variation","end":140425389,"alleles":["C","T"]},{"id":"rs1409801227","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140425391,"strand":1,"feature_type":"variation","start":140425391,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1799645387","seq_region_name":"7","clinical_significance":[],"end":140425393,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140425393,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs568812355","feature_type":"variation","strand":1,"end":140425396,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425396},{"seq_region_name":"7","id":"rs1166047867","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425397,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140425397},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799645557","feature_type":"variation","strand":1,"alleles":["CTCT","CT"],"end":140425401,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425398},{"end":140425400,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140425400,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1044595175"},{"source":"dbSNP","start":140425402,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140425402,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs529817269"},{"start":140425404,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140425404,"strand":1,"feature_type":"variation","id":"rs187066955","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1480748574","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","-"],"end":140425404,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425404,"source":"dbSNP"},{"seq_region_name":"7","id":"rs761249568","clinical_significance":[],"alleles":["G","A"],"end":140425405,"strand":1,"feature_type":"variation","start":140425405,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140425406,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140425406,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs376247534","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140425407,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425407,"source":"dbSNP","seq_region_name":"7","id":"rs1799646008","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425411,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140425411,"clinical_significance":[],"id":"rs1234306646","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425411,"feature_type":"variation","strand":1,"end":140425415,"alleles":["GGGGG","GGGG"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799646142"},{"seq_region_name":"7","id":"rs1227503239","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425413,"source":"dbSNP","strand":1,"feature_type":"variation","end":140425413,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1799646256","clinical_significance":[],"alleles":["G","A"],"end":140425415,"strand":1,"feature_type":"variation","start":140425415,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140425416,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140425416,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs868239318"},{"alleles":["A","G"],"end":140425418,"strand":1,"feature_type":"variation","start":140425418,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1312320440","clinical_significance":[]},{"seq_region_name":"7","id":"rs781392477","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425418,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AAAAA","AAA"],"end":140425422},{"seq_region_name":"7","id":"rs1799646495","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425418,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AAAAAGAGAGTAAAAAGAG","AAAAAGAGAGTAAAAAGAGAGTAAAAAGAG"],"end":140425436},{"seq_region_name":"7","id":"rs1799646547","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425422,"source":"dbSNP","strand":1,"feature_type":"variation","end":140425422,"alleles":["A","G"]},{"end":140425427,"alleles":["AGAGAG","AGAG"],"strand":1,"feature_type":"variation","start":140425422,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130172361","clinical_significance":[]},{"source":"dbSNP","start":140425425,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140425425,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799646595"},{"id":"rs1799646639","seq_region_name":"7","clinical_significance":[],"alleles":["A","G"],"end":140425431,"strand":1,"feature_type":"variation","start":140425431,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799646684","end":140425434,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140425434,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["G","C"],"end":140425437,"strand":1,"feature_type":"variation","start":140425437,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs950938536","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425438,"source":"dbSNP","strand":1,"feature_type":"variation","end":140425438,"alleles":["A","G"],"id":"rs796756083","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425440,"feature_type":"variation","strand":1,"end":140425440,"alleles":["C","T"],"clinical_significance":[],"id":"rs1230719241","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799646920","clinical_significance":[],"strand":1,"feature_type":"variation","end":140425447,"alleles":["CC","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425446,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1017187891","clinical_significance":[],"start":140425447,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140425447,"alleles":["C","G","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799647027","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425449,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140425449},{"seq_region_name":"7","id":"rs1799647080","clinical_significance":[],"start":140425449,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["GGTGCAGTGGCTCATGCCTATAATCCCAGCACTTTCGGAGGCCG","G"],"end":140425492,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799647131","source":"dbSNP","start":140425450,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["GTGCAGTGGCTCATGCCTATAATCCCAGCACTTTCGGAGGCCG","G"],"end":140425492,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799647185","source":"dbSNP","start":140425457,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140425457,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs962536622","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425461,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140425461},{"feature_type":"variation","strand":1,"end":140425465,"alleles":["C","A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425465,"clinical_significance":[],"seq_region_name":"7","id":"rs1799647284"},{"source":"dbSNP","start":140425468,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140425468,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1585436394","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799647395","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140425472,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425472,"source":"dbSNP"},{"start":140425477,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140425477,"alleles":["G","C"],"strand":1,"feature_type":"variation","id":"rs1224460893","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140425484,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425484,"clinical_significance":[],"id":"rs1019274589","seq_region_name":"7"},{"alleles":["G","A","T"],"end":140425485,"strand":1,"feature_type":"variation","start":140425485,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs994405063","clinical_significance":[]},{"start":140425488,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140425488,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs975539483","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130172566","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140425489,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425489,"source":"dbSNP"},{"start":140425491,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","T"],"end":140425491,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs4726806","clinical_significance":[]},{"clinical_significance":[],"id":"rs570733827","seq_region_name":"7","source":"dbSNP","start":140425492,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140425492,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1181588018","source":"dbSNP","start":140425498,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140425498,"alleles":["G","A"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140425500,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425500,"clinical_significance":[],"seq_region_name":"7","id":"rs955255843"},{"seq_region_name":"7","id":"rs987486552","clinical_significance":[],"start":140425501,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140425501,"alleles":["G","A","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs911866785","seq_region_name":"7","alleles":["T","A"],"end":140425503,"feature_type":"variation","strand":1,"source":"dbSNP","start":140425503,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["A","C"],"end":140425505,"strand":1,"feature_type":"variation","start":140425505,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585436474","clinical_significance":[]},{"start":140425506,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140425506,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs965164853","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140425507,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425507,"clinical_significance":[],"seq_region_name":"7","id":"rs1799648190"},{"end":140425511,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140425511,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1799648239","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799648291","feature_type":"variation","strand":1,"end":140425512,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425512},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799648347","feature_type":"variation","strand":1,"alleles":["GG","GGGG"],"end":140425517,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425516},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425517,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140425517,"seq_region_name":"7","id":"rs974813422","clinical_significance":[]},{"id":"rs1799648461","seq_region_name":"7","clinical_significance":[],"alleles":["G","C"],"end":140425519,"strand":1,"feature_type":"variation","start":140425519,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799648516","source":"dbSNP","start":140425522,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140425522,"alleles":["C","G"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140425523,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425523,"source":"dbSNP","seq_region_name":"7","id":"rs1799648560","clinical_significance":[]},{"seq_region_name":"7","id":"rs1409658846","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140425524,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425524,"source":"dbSNP"},{"source":"dbSNP","start":140425526,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140425526,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585436491"},{"seq_region_name":"7","id":"rs1419802845","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425533,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140425533},{"feature_type":"variation","strand":1,"end":140425534,"alleles":["G","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425534,"clinical_significance":[],"seq_region_name":"7","id":"rs1175143076"},{"end":140425535,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140425535,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799648842"},{"seq_region_name":"7","id":"rs1585436506","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140425540,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425540,"source":"dbSNP"},{"id":"rs549446493","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140425542,"alleles":["T","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425542,"source":"dbSNP"},{"end":140425543,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140425543,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1269339657","clinical_significance":[]},{"alleles":["G","A"],"end":140425544,"feature_type":"variation","strand":1,"source":"dbSNP","start":140425544,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1166322452"},{"source":"dbSNP","start":140425545,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140425545,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1224534502","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425548,"feature_type":"variation","strand":1,"end":140425548,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799649117"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425550,"feature_type":"variation","strand":1,"end":140425550,"alleles":["C","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799649171"},{"start":140425551,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140425551,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585436532","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799649294","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425553,"feature_type":"variation","strand":1,"alleles":["CTTCT","CT"],"end":140425557},{"clinical_significance":[],"id":"rs1585436535","seq_region_name":"7","source":"dbSNP","start":140425554,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140425554,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs936215997","clinical_significance":[],"strand":1,"feature_type":"variation","end":140425556,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425556,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1291008325","seq_region_name":"7","alleles":["T","C"],"end":140425559,"feature_type":"variation","strand":1,"source":"dbSNP","start":140425559,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799649505","feature_type":"variation","strand":1,"alleles":["A","T"],"end":140425560,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425560},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140425561,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425561,"clinical_significance":[],"seq_region_name":"7","id":"rs12216582"},{"id":"rs574807494","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425563,"source":"dbSNP","strand":1,"feature_type":"variation","end":140425563,"alleles":["A","G"]},{"end":140425563,"alleles":["A","AGA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140425563,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1585436567","seq_region_name":"7"},{"id":"rs1799649793","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425565,"source":"dbSNP","strand":1,"feature_type":"variation","end":140425565,"alleles":["A","C"]},{"source":"dbSNP","start":140425568,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140425568,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs750862989"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799649902","source":"dbSNP","start":140425570,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140425570,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1799649944","clinical_significance":[],"start":140425571,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AAAA","AAAAA"],"end":140425574,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799650002","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425572,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140425572},{"clinical_significance":[],"id":"rs1799650052","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140425575,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425575},{"seq_region_name":"7","id":"rs112727882","clinical_significance":[],"start":140425580,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140425580,"alleles":["C","A","T"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140425581,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425581,"source":"dbSNP","seq_region_name":"7","id":"rs905504148","clinical_significance":[]},{"source":"dbSNP","start":140425584,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140425584,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1285576088"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1001693881","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425585,"feature_type":"variation","strand":1,"end":140425585,"alleles":["G","A"]},{"start":140425590,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140425590,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1038162746","clinical_significance":[]},{"alleles":["C","T"],"end":140425592,"feature_type":"variation","strand":1,"source":"dbSNP","start":140425592,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130173044"},{"clinical_significance":[],"id":"rs1290001750","seq_region_name":"7","feature_type":"variation","strand":1,"end":140425593,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425593},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140425594,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425594,"clinical_significance":[],"id":"rs1799650436","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140425596,"alleles":["T","A","C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425596,"clinical_significance":[],"seq_region_name":"7","id":"rs898232012"},{"id":"rs948842631","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425608,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140425608},{"source":"dbSNP","start":140425609,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140425609,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799651092"},{"seq_region_name":"7","id":"rs1799651135","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425610,"source":"dbSNP","strand":1,"feature_type":"variation","end":140425610,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799651192","end":140425612,"alleles":["GCT","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140425610,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1799651235","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140425615,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425615,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799651291","end":140425622,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140425622,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs994045483","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425623,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140425623},{"alleles":["G","A"],"end":140425627,"strand":1,"feature_type":"variation","start":140425627,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1456376910","clinical_significance":[]},{"alleles":["C","T"],"end":140425629,"feature_type":"variation","strand":1,"source":"dbSNP","start":140425629,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799651447"},{"end":140425632,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140425632,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs780871727","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425633,"feature_type":"variation","strand":1,"end":140425633,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585436655"},{"source":"dbSNP","start":140425637,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140425637,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1437631439"},{"id":"rs1201284712","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140425638,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425638,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140425639,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425639,"source":"dbSNP","id":"rs1799651704","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1554442921","alleles":["GCTTGAACCTGG","G"],"end":140425650,"feature_type":"variation","strand":1,"source":"dbSNP","start":140425639,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140425643,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140425643,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs796486163"},{"source":"dbSNP","start":140425648,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140425648,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799651863"},{"seq_region_name":"7","id":"rs1025458267","clinical_significance":[],"end":140425650,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140425650,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425654,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140425654,"seq_region_name":"7","id":"rs1799651966","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs113294097","end":140425655,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140425655,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1219843633","clinical_significance":[],"start":140425656,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140425656,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425661,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140425661,"seq_region_name":"7","id":"rs1585436698","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799652171","clinical_significance":[],"strand":1,"feature_type":"variation","end":140425663,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425663,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425665,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140425665,"clinical_significance":[],"id":"rs1008113937","seq_region_name":"7"},{"alleles":["A","G"],"end":140425666,"strand":1,"feature_type":"variation","start":140425666,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585436705","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140425669,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425669,"clinical_significance":[],"seq_region_name":"7","id":"rs1799652332"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1281372950","source":"dbSNP","start":140425673,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140425673,"alleles":["A","G"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140425674,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425674,"clinical_significance":[],"seq_region_name":"7","id":"rs1486856096"},{"id":"rs796708398","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140425679,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425679,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1018956923","clinical_significance":[],"start":140425680,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140425680,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1799652567","clinical_significance":[],"end":140425681,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140425681,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs189365871","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140425683,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425683,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs763499569","source":"dbSNP","start":140425686,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140425686,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140425689,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140425689,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585436738"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425692,"feature_type":"variation","strand":1,"end":140425692,"alleles":["C","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130173469"},{"end":140425696,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140425696,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799652786"},{"seq_region_name":"7","id":"rs541241033","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425700,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140425700},{"strand":1,"feature_type":"variation","end":140425702,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425702,"source":"dbSNP","seq_region_name":"7","id":"rs546509211","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425703,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140425703,"clinical_significance":[],"seq_region_name":"7","id":"rs1222023624"},{"seq_region_name":"7","id":"rs1799653017","clinical_significance":[],"alleles":["G","C"],"end":140425708,"strand":1,"feature_type":"variation","start":140425708,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140425710,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140425710,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1799653072","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130173559","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140425711,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425711,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130173572","feature_type":"variation","strand":1,"end":140425714,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425714},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130173587","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425715,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140425715},{"alleles":["C","T"],"end":140425716,"strand":1,"feature_type":"variation","start":140425716,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1837070224","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs564581743","clinical_significance":[],"end":140425719,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140425719,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs532033123","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425720,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140425720},{"clinical_significance":[],"id":"rs1799653221","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425723,"feature_type":"variation","strand":1,"end":140425723,"alleles":["T","A"]},{"alleles":["-","AA"],"end":140425723,"feature_type":"variation","strand":1,"source":"dbSNP","start":140425724,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799653265"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425724,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140425724,"clinical_significance":[],"id":"rs201394715","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs71761236","feature_type":"variation","strand":1,"alleles":["AAAAAAAAAAA","AAAAAAAAAA","AAAAAAAAAAAA","AAAAAAAAAAAAA","AAAAAAAAAAAAAA"],"end":140425735,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425725},{"seq_region_name":"7","id":"rs1406310790","clinical_significance":[],"alleles":["A","AGA"],"end":140425729,"strand":1,"feature_type":"variation","start":140425729,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs543624397","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140425732,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425732},{"clinical_significance":[],"seq_region_name":"7","id":"rs1178174887","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425733,"feature_type":"variation","strand":1,"end":140425734,"alleles":["AA","AAGAA"]},{"seq_region_name":"7","id":"rs1186339004","clinical_significance":[],"start":140425736,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140425736,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425736,"feature_type":"variation","strand":1,"end":140425736,"alleles":["G","GG"],"clinical_significance":[],"seq_region_name":"7","id":"rs1467989402"},{"seq_region_name":"7","id":"rs1247002233","clinical_significance":[],"strand":1,"feature_type":"variation","end":140425740,"alleles":["C","A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425740,"source":"dbSNP"},{"id":"rs1799653894","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["AAAAAAA","AAAAAAAA"],"end":140425747,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425741,"source":"dbSNP"},{"seq_region_name":"7","id":"rs975139811","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425748,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140425748},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140425756,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425756,"clinical_significance":[],"id":"rs1033125534","seq_region_name":"7"},{"id":"rs370473100","seq_region_name":"7","clinical_significance":[],"start":140425758,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140425758,"strand":1,"feature_type":"variation"},{"end":140425760,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140425760,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1430232788"},{"seq_region_name":"7","id":"rs1259642464","clinical_significance":[],"end":140425762,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140425762,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140425763,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140425763,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs994969223","clinical_significance":[]},{"seq_region_name":"7","id":"rs562323535","clinical_significance":[],"end":140425764,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140425764,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs988959119","feature_type":"variation","strand":1,"end":140425765,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425765},{"seq_region_name":"7","id":"rs1799654426","clinical_significance":[],"strand":1,"feature_type":"variation","end":140425767,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425767,"source":"dbSNP"},{"id":"rs2130173978","seq_region_name":"7","clinical_significance":[],"alleles":["T","A"],"end":140425769,"strand":1,"feature_type":"variation","start":140425769,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["G","A"],"end":140425770,"feature_type":"variation","strand":1,"source":"dbSNP","start":140425770,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs547384873"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425774,"feature_type":"variation","strand":1,"alleles":["G","C","T"],"end":140425774,"clinical_significance":[],"seq_region_name":"7","id":"rs1173771449"},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140425775,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425775,"clinical_significance":[],"seq_region_name":"7","id":"rs1799654602"},{"strand":1,"feature_type":"variation","end":140425778,"alleles":["G","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425778,"source":"dbSNP","seq_region_name":"7","id":"rs886716299","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585436859","clinical_significance":[],"start":140425778,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140425778,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1344677073","source":"dbSNP","start":140425780,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140425780,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140425781,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425781,"source":"dbSNP","seq_region_name":"7","id":"rs913375954","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799654868","clinical_significance":[],"start":140425783,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140425783,"strand":1,"feature_type":"variation"},{"id":"rs1230157753","seq_region_name":"7","clinical_significance":[],"alleles":["A","C"],"end":140425784,"strand":1,"feature_type":"variation","start":140425784,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425785,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140425785,"clinical_significance":[],"id":"rs1306244145","seq_region_name":"7"},{"source":"dbSNP","start":140425786,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140425786,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs950313558"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425787,"source":"dbSNP","strand":1,"feature_type":"variation","end":140425787,"alleles":["C","T"],"seq_region_name":"7","id":"rs1019305923","clinical_significance":[]},{"source":"dbSNP","start":140425790,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140425790,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs180684779"},{"clinical_significance":[],"seq_region_name":"7","id":"rs996613503","alleles":["T","C"],"end":140425791,"feature_type":"variation","strand":1,"source":"dbSNP","start":140425791,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140425794,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140425794,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799655224"},{"id":"rs1338230572","seq_region_name":"7","clinical_significance":[],"end":140425796,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140425796,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1028458167","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425799,"source":"dbSNP","strand":1,"feature_type":"variation","end":140425799,"alleles":["C","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425800,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140425800,"clinical_significance":[],"seq_region_name":"7","id":"rs1799655374"},{"seq_region_name":"7","id":"rs1799655420","clinical_significance":[],"strand":1,"feature_type":"variation","end":140425805,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425805,"source":"dbSNP"},{"end":140425810,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140425810,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130174188","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799655470","end":140425812,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140425812,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799655526","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140425813,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425813},{"seq_region_name":"7","id":"rs1401138298","clinical_significance":[],"start":140425814,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140425814,"strand":1,"feature_type":"variation"},{"end":140425815,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140425815,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1298520003"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425818,"feature_type":"variation","strand":1,"end":140425818,"alleles":["G","T"],"clinical_significance":[],"id":"rs1799655683","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs968490516","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425823,"feature_type":"variation","strand":1,"alleles":["TTTT","TTTTTT"],"end":140425826},{"strand":1,"feature_type":"variation","end":140425824,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425824,"source":"dbSNP","seq_region_name":"7","id":"rs1585436931","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425826,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140425826,"seq_region_name":"7","id":"rs1371229557","clinical_significance":[]},{"source":"dbSNP","start":140425827,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140425827,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs978603450","seq_region_name":"7"},{"source":"dbSNP","start":140425828,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140425828,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799655946"},{"seq_region_name":"7","id":"rs1445253535","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425830,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140425830},{"source":"dbSNP","start":140425834,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140425834,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs758519967"},{"clinical_significance":[],"seq_region_name":"7","id":"rs572198586","source":"dbSNP","start":140425852,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140425852,"feature_type":"variation","strand":1},{"alleles":["G","A"],"end":140425855,"strand":1,"feature_type":"variation","start":140425855,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799656137","clinical_significance":[]},{"start":140425858,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140425858,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs747013868","clinical_significance":[]},{"seq_region_name":"7","id":"rs771057610","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425859,"source":"dbSNP","strand":1,"feature_type":"variation","end":140425859,"alleles":["A","G"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425861,"source":"dbSNP","strand":1,"feature_type":"variation","end":140425861,"alleles":["C","T"],"seq_region_name":"7","id":"rs74881626","clinical_significance":[]},{"seq_region_name":"7","id":"rs527254799","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140425862,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140425862},{"source":"dbSNP","start":140425863,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140425863,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1313049398"},{"end":140425866,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140425866,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_polypyrimidine_tract_variant","seq_region_name":"7","id":"rs1799656470","clinical_significance":[]},{"seq_region_name":"7","id":"rs1327749229","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140425874,"assembly_name":"GRCh38","consequence_type":"splice_region_variant","start":140425874,"source":"dbSNP"},{"seq_region_name":"7","id":"rs768762322","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"splice_region_variant","start":140425879,"source":"dbSNP","strand":1,"feature_type":"variation","end":140425879,"alleles":["C","G"]},{"clinical_significance":[],"id":"rs1799656608","seq_region_name":"7","end":140425880,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140425880,"consequence_type":"splice_acceptor_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1251580589","seq_region_name":"7","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425886,"feature_type":"variation","strand":1,"end":140425886,"alleles":["T","A"]},{"end":140425890,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140425890,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs774254709"},{"alleles":["G","A"],"end":140425891,"feature_type":"variation","strand":1,"source":"dbSNP","start":140425891,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs761696770"},{"id":"rs955985079","seq_region_name":"7","clinical_significance":[],"start":140425894,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["A","C"],"end":140425894,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799656902","end":140425895,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140425895,"consequence_type":"synonymous_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140425896,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140425896,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799656965"},{"end":140425897,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140425897,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs771572401"},{"seq_region_name":"7","id":"rs772928313","clinical_significance":[],"alleles":["T","C"],"end":140425899,"strand":1,"feature_type":"variation","start":140425899,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs992672973","source":"dbSNP","start":140425900,"consequence_type":"frameshift_variant","assembly_name":"GRCh38","end":140425902,"alleles":["GGG","GG"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs760033770","clinical_significance":[],"start":140425901,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"stop_gained","end":140425901,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs2130174586","clinical_significance":[],"strand":1,"feature_type":"variation","end":140425902,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140425902,"source":"dbSNP"},{"start":140425903,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["A","G"],"end":140425903,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs375344241","clinical_significance":[]},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425905,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140425905,"clinical_significance":["uncertain significance"],"id":"rs1274483320","seq_region_name":"7"},{"end":140425908,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140425908,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs753408586"},{"alleles":["G","A"],"end":140425909,"strand":1,"feature_type":"variation","start":140425909,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs760017924","clinical_significance":["uncertain significance"]},{"start":140425910,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","alleles":["G","T"],"end":140425910,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1416302073","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140425913,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425913,"clinical_significance":[],"id":"rs138475915","seq_region_name":"7"},{"seq_region_name":"7","id":"rs752965955","clinical_significance":[],"start":140425914,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["G","A"],"end":140425914,"strand":1,"feature_type":"variation"},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425915,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140425915,"clinical_significance":[],"id":"rs1391195670","seq_region_name":"7"},{"start":140425916,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","end":140425916,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs758815097","clinical_significance":[]},{"seq_region_name":"7","id":"rs898261798","clinical_significance":[],"start":140425918,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["T","C"],"end":140425918,"strand":1,"feature_type":"variation"},{"end":140425920,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140425920,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs777801769","clinical_significance":[]},{"alleles":["C","T"],"end":140425922,"strand":1,"feature_type":"variation","start":140425922,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","seq_region_name":"7","id":"rs751811948","clinical_significance":[]},{"source":"dbSNP","start":140425923,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140425923,"feature_type":"variation","strand":1,"clinical_significance":["uncertain significance"],"seq_region_name":"7","id":"rs570628599"},{"seq_region_name":"7","id":"rs1799658236","clinical_significance":["uncertain significance"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140425926,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140425926},{"start":140425928,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["T","G"],"end":140425928,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799658300","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs745983601","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425930,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140425930},{"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140425931,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140425931,"id":"rs557959190","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs768672408","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425935,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140425935},{"seq_region_name":"7","id":"rs1226273770","clinical_significance":[],"start":140425937,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","alleles":["A","G"],"end":140425937,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140425943,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140425943,"seq_region_name":"7","id":"rs373556406","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140425946,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140425946,"seq_region_name":"7","id":"rs2130174929","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140425950,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140425950,"source":"dbSNP","seq_region_name":"7","id":"rs2948386","clinical_significance":[]},{"start":140425951,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140425951,"alleles":["A","G"],"strand":1,"feature_type":"variation","id":"rs747837185","seq_region_name":"7","clinical_significance":[]},{"id":"rs890924639","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"stop_gained","start":140425952,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140425952},{"seq_region_name":"7","id":"rs771901851","clinical_significance":["uncertain significance"],"start":140425953,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["G","A"],"end":140425953,"strand":1,"feature_type":"variation"},{"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425958,"feature_type":"variation","strand":1,"end":140425958,"alleles":["C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799659157"},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140425960,"source":"dbSNP","strand":1,"feature_type":"variation","end":140425960,"alleles":["T","C"],"seq_region_name":"7","id":"rs772942378","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs370140812","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425963,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140425963},{"seq_region_name":"7","id":"rs141552535","clinical_significance":[],"start":140425964,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","alleles":["C","T"],"end":140425964,"strand":1,"feature_type":"variation"},{"id":"rs568276754","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140425965,"source":"dbSNP","strand":1,"feature_type":"variation","end":140425965,"alleles":["G","A","T"]},{"source":"dbSNP","start":140425967,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140425967,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs200790536"},{"source":"dbSNP","start":140425968,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140425968,"alleles":["T","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs765685964","seq_region_name":"7"},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425972,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140425972,"clinical_significance":[],"seq_region_name":"7","id":"rs1799659688"},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140425974,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140425974,"seq_region_name":"7","id":"rs1799659757","clinical_significance":[]},{"clinical_significance":[],"id":"rs755123670","seq_region_name":"7","alleles":["A","G"],"end":140425976,"feature_type":"variation","strand":1,"source":"dbSNP","start":140425976,"consequence_type":"synonymous_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1040990196","clinical_significance":[],"end":140425977,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140425977,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"seq_region_name":"7","id":"rs1167249451","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140425978,"source":"dbSNP","strand":1,"feature_type":"variation","end":140425978,"alleles":["C","G"]},{"feature_type":"variation","strand":1,"end":140425980,"alleles":["G","A"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425980,"clinical_significance":[],"seq_region_name":"7","id":"rs1799660065"},{"id":"rs1419515548","seq_region_name":"7","clinical_significance":[],"start":140425981,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140425981,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"end":140425984,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140425984,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs763161215","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799660249","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425986,"feature_type":"variation","strand":1,"end":140425986,"alleles":["G","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs764514529","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140425990,"consequence_type":"stop_gained","assembly_name":"GRCh38","source":"dbSNP","start":140425990},{"start":140425996,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140425996,"alleles":["A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs751917314","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140425997,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425997,"clinical_significance":[],"seq_region_name":"7","id":"rs757521106"},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425998,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140425998,"clinical_significance":[],"id":"rs767881775","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140425999,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140425999,"clinical_significance":[],"seq_region_name":"7","id":"rs574686417"},{"seq_region_name":"7","id":"rs756273120","clinical_significance":[],"start":140426000,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","end":140426000,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"inframe_deletion","start":140426000,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AGAAGAAG","AGAAG"],"end":140426007,"seq_region_name":"7","id":"rs751346314","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1437082644","end":140426001,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140426001,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426006,"feature_type":"variation","strand":1,"end":140426006,"alleles":["A","G"],"clinical_significance":[],"id":"rs1295307281","seq_region_name":"7"},{"alleles":["T","A"],"end":140426008,"strand":1,"feature_type":"variation","start":140426008,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs1799661051","clinical_significance":[]},{"start":140426009,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","end":140426009,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs778646799","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140426012,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140426012,"source":"dbSNP","id":"rs371818531","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs146383208","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140426013,"source":"dbSNP","strand":1,"feature_type":"variation","end":140426013,"alleles":["G","A"]},{"strand":1,"feature_type":"variation","end":140426015,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140426015,"source":"dbSNP","seq_region_name":"7","id":"rs746823898","clinical_significance":[]},{"source":"dbSNP","start":140426017,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140426017,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1203247207","seq_region_name":"7"},{"source":"dbSNP","start":140426019,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["A","C","G","T"],"end":140426019,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1279712789"},{"start":140426020,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["T","A"],"end":140426020,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1269074412","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799661742","end":140426026,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140426026,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs957491901","clinical_significance":[],"end":140426028,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140426028,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"stop_gained"},{"strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140426029,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140426029,"source":"dbSNP","seq_region_name":"7","id":"rs988823882","clinical_significance":[]},{"source":"dbSNP","start":140426031,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140426031,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1235160729","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"protein_altering_variant","start":140426032,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TGAT","TGATGAT"],"end":140426035,"id":"rs1563076322","seq_region_name":"7","clinical_significance":[]},{"end":140426033,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140426033,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs770533578"},{"clinical_significance":[],"seq_region_name":"7","id":"rs776290345","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426036,"feature_type":"variation","strand":1,"end":140426036,"alleles":["C","G","T"]},{"clinical_significance":[],"id":"rs745326291","seq_region_name":"7","feature_type":"variation","strand":1,"end":140426037,"alleles":["G","A","C"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426037},{"source":"dbSNP","start":140426038,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140426038,"feature_type":"variation","strand":1,"clinical_significance":["uncertain significance"],"seq_region_name":"7","id":"rs554346458"},{"clinical_significance":[],"seq_region_name":"7","id":"rs4726807","source":"dbSNP","start":140426039,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140426039,"feature_type":"variation","strand":1},{"alleles":["C","T"],"end":140426040,"strand":1,"feature_type":"variation","start":140426040,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","id":"rs764549397","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140426041,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["G","A","C","T"],"end":140426041,"feature_type":"variation","strand":1,"clinical_significance":["uncertain significance"],"seq_region_name":"7","id":"rs558153548"},{"start":140426047,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["G","T"],"end":140426047,"strand":1,"feature_type":"variation","id":"rs762290218","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426049,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140426049,"clinical_significance":[],"id":"rs1442584931","seq_region_name":"7"},{"end":140426051,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140426051,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799663092"},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426053,"feature_type":"variation","strand":1,"end":140426053,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1554443009"},{"seq_region_name":"7","id":"rs1451888842","clinical_significance":[],"start":140426054,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","end":140426054,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs761726370","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"inframe_deletion","start":140426054,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CCTATATGGGGAGAGTGCCCT","CCT"],"end":140426074},{"alleles":["A","C"],"end":140426057,"strand":1,"feature_type":"variation","start":140426057,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","id":"rs2130175987","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140426058,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140426058,"feature_type":"variation","strand":1,"clinical_significance":["uncertain significance"],"id":"rs144022880","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140426059,"alleles":["A","G"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426059,"clinical_significance":[],"id":"rs1458491429","seq_region_name":"7"},{"end":140426062,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140426062,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs2130176022","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140426066,"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140426066,"source":"dbSNP","seq_region_name":"7","id":"rs368405538","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140426068,"alleles":["G","T"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426068,"clinical_significance":[],"seq_region_name":"7","id":"rs1315888324"},{"start":140426069,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140426069,"alleles":["T","A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1325660696","clinical_significance":["uncertain significance"]},{"alleles":["C","T"],"end":140426071,"strand":1,"feature_type":"variation","start":140426071,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs1411579062","clinical_significance":[]},{"end":140426072,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140426072,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","seq_region_name":"7","id":"rs750675356","clinical_significance":[]},{"start":140426074,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["T","A","C"],"end":140426074,"strand":1,"feature_type":"variation","id":"rs992707189","seq_region_name":"7","clinical_significance":[]},{"end":140426075,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140426075,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","seq_region_name":"7","id":"rs544128497","clinical_significance":[]},{"end":140426078,"alleles":["C","A","G","T"],"strand":1,"feature_type":"variation","start":140426078,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs4585665","clinical_significance":[]},{"seq_region_name":"7","id":"rs144362151","clinical_significance":[],"start":140426079,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["G","A"],"end":140426079,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1284341250","clinical_significance":[],"alleles":["C","T"],"end":140426081,"strand":1,"feature_type":"variation","start":140426081,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant"},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426083,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140426083,"clinical_significance":[],"seq_region_name":"7","id":"rs1799664506"},{"clinical_significance":[],"seq_region_name":"7","id":"rs148741038","consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426084,"feature_type":"variation","strand":1,"end":140426084,"alleles":["C","G","T"]},{"id":"rs1799664664","seq_region_name":"7","clinical_significance":[],"start":140426085,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"inframe_deletion","end":140426106,"alleles":["CCCCTGGACTCCAGCCCCGTTC","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs529487725","seq_region_name":"7","consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426087,"feature_type":"variation","strand":1,"alleles":["C","A","G","T"],"end":140426087},{"id":"rs777605625","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140426088,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140426088,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1207086674","source":"dbSNP","start":140426091,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140426091,"feature_type":"variation","strand":1},{"id":"rs1223852264","seq_region_name":"7","clinical_significance":[],"start":140426092,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140426092,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"start":140426093,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","end":140426093,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs746760092","clinical_significance":[]},{"clinical_significance":[],"id":"rs1325451305","seq_region_name":"7","alleles":["T","-"],"end":140426094,"feature_type":"variation","strand":1,"source":"dbSNP","start":140426094,"consequence_type":"frameshift_variant","assembly_name":"GRCh38"},{"id":"rs1272939081","seq_region_name":"7","clinical_significance":[],"alleles":["A","T"],"end":140426097,"strand":1,"feature_type":"variation","start":140426097,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"seq_region_name":"7","id":"rs969991438","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["CCCC","CCC"],"end":140426102,"assembly_name":"GRCh38","consequence_type":"frameshift_variant","start":140426099,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs757058982","source":"dbSNP","start":140426101,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140426101,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1224394286","feature_type":"variation","strand":1,"end":140426102,"alleles":["C","T"],"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426102},{"id":"rs144754394","seq_region_name":"7","clinical_significance":[],"start":140426103,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["G","A","T"],"end":140426103,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1298374842","consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426108,"feature_type":"variation","strand":1,"end":140426108,"alleles":["T","C"]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140426110,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140426110,"source":"dbSNP","seq_region_name":"7","id":"rs1563076461","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140426111,"source":"dbSNP","strand":1,"feature_type":"variation","end":140426111,"alleles":["G","A","T"],"seq_region_name":"7","id":"rs147871231","clinical_significance":[]},{"id":"rs1197980303","seq_region_name":"7","clinical_significance":[],"alleles":["C","A"],"end":140426113,"strand":1,"feature_type":"variation","start":140426113,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs769391130","consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426114,"feature_type":"variation","strand":1,"end":140426114,"alleles":["C","T"]},{"start":140426116,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140426116,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1473339449","clinical_significance":[]},{"end":140426118,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140426118,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs1327142718","clinical_significance":[]},{"start":140426122,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["C","G","T"],"end":140426122,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs775034178","clinical_significance":[]},{"clinical_significance":[],"id":"rs748779977","seq_region_name":"7","alleles":["A","C","T"],"end":140426123,"feature_type":"variation","strand":1,"source":"dbSNP","start":140426123,"consequence_type":"synonymous_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs769155753","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140426124,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140426124,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1325441561","clinical_significance":[],"start":140426125,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["G","T"],"end":140426125,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs774732290","source":"dbSNP","start":140426126,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140426126,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563076498","consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426135,"feature_type":"variation","strand":1,"end":140426135,"alleles":["C","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1363571185","source":"dbSNP","start":140426136,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140426136,"alleles":["C","T"],"feature_type":"variation","strand":1},{"alleles":["A","-"],"end":140426142,"strand":1,"feature_type":"variation","start":140426142,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"frameshift_variant","seq_region_name":"7","id":"rs767038237","clinical_significance":[]},{"id":"rs1172427827","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140426142,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140426142,"source":"dbSNP"},{"alleles":["T","C"],"end":140426144,"strand":1,"feature_type":"variation","start":140426144,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","seq_region_name":"7","id":"rs1476022119","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"stop_retained_variant","start":140426149,"source":"dbSNP","strand":1,"feature_type":"variation","end":140426149,"alleles":["A","G"],"seq_region_name":"7","id":"rs1244385950","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799668128","clinical_significance":[],"alleles":["A","G"],"end":140426150,"strand":1,"feature_type":"variation","start":140426150,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"stop_retained_variant"},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426161,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140426161,"clinical_significance":[],"seq_region_name":"7","id":"rs1799668193"},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426164,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140426164,"clinical_significance":[],"id":"rs772202993","seq_region_name":"7"},{"start":140426166,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140426166,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs920594096","clinical_significance":[]},{"start":140426168,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["T","C"],"end":140426168,"strand":1,"feature_type":"variation","id":"rs1799668373","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1463188558","feature_type":"variation","strand":1,"alleles":["GCACCCAC","-"],"end":140426177,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426170},{"feature_type":"variation","strand":1,"end":140426172,"alleles":["A","C","G"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426172,"clinical_significance":[],"seq_region_name":"7","id":"rs1352444500"},{"seq_region_name":"7","id":"rs762198519","clinical_significance":[],"start":140426173,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["C","T"],"end":140426173,"strand":1,"feature_type":"variation"},{"alleles":["CCC","CC"],"end":140426175,"strand":1,"feature_type":"variation","start":140426173,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs1246974983","clinical_significance":[]},{"clinical_significance":[],"id":"rs772558753","seq_region_name":"7","end":140426178,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140426178,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs370265932","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426180,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140426180},{"end":140426186,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140426186,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1230449724"},{"clinical_significance":[],"seq_region_name":"7","id":"rs760953309","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426187,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140426187},{"clinical_significance":[],"seq_region_name":"7","id":"rs527407531","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426188,"feature_type":"variation","strand":1,"end":140426188,"alleles":["G","A","T"]},{"source":"dbSNP","start":140426189,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140426189,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs753917927"},{"alleles":["A","C"],"end":140426202,"strand":1,"feature_type":"variation","start":140426202,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs759559568","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799669778","seq_region_name":"7","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426211,"feature_type":"variation","strand":1,"end":140426211,"alleles":["G","A"]},{"start":140426211,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140426218,"alleles":["GGATACCG","G"],"strand":1,"feature_type":"variation","id":"rs1799669835","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426214,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140426214,"id":"rs1039537531","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426217,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140426217,"clinical_significance":[],"seq_region_name":"7","id":"rs908046452"},{"seq_region_name":"7","id":"rs899767824","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426218,"source":"dbSNP","strand":1,"feature_type":"variation","end":140426218,"alleles":["G","A"]},{"clinical_significance":[],"id":"rs1799670021","seq_region_name":"7","alleles":["T","C"],"end":140426222,"feature_type":"variation","strand":1,"source":"dbSNP","start":140426222,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426227,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140426227,"clinical_significance":[],"seq_region_name":"7","id":"rs1799670073"},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426229,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140426229,"clinical_significance":[],"id":"rs1001163432","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799670178","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140426234,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426234,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1205190663","clinical_significance":[],"alleles":["G","A"],"end":140426235,"strand":1,"feature_type":"variation","start":140426235,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs944824743","source":"dbSNP","start":140426236,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140426236,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs551856243","seq_region_name":"7","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426237,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140426237},{"start":140426238,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["C","T"],"end":140426238,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799670392","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1454777802","source":"dbSNP","start":140426242,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140426242,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426244,"source":"dbSNP","strand":1,"feature_type":"variation","end":140426244,"alleles":["A","T"],"seq_region_name":"7","id":"rs1040540718","clinical_significance":[]},{"source":"dbSNP","start":140426245,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140426245,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1054470940"},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426247,"feature_type":"variation","strand":1,"end":140426247,"alleles":["C","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799670547"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1410922328","alleles":["C","T"],"end":140426248,"feature_type":"variation","strand":1,"source":"dbSNP","start":140426248,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"alleles":["A","G","T"],"end":140426249,"feature_type":"variation","strand":1,"source":"dbSNP","start":140426249,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs746816116","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs564146396","source":"dbSNP","start":140426251,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140426251,"alleles":["C","A","T"],"feature_type":"variation","strand":1},{"end":140426252,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140426252,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs768376469"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799670849","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426253,"feature_type":"variation","strand":1,"end":140426253,"alleles":["T","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799670909","source":"dbSNP","start":140426254,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140426254,"alleles":["G","A"],"feature_type":"variation","strand":1},{"alleles":["GG","GGG"],"end":140426255,"feature_type":"variation","strand":1,"source":"dbSNP","start":140426254,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1389012305"},{"source":"dbSNP","start":140426255,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140426255,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799671073"},{"clinical_significance":[],"seq_region_name":"7","id":"rs144381871","end":140426262,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140426262,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426263,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140426263,"seq_region_name":"7","id":"rs112566891","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140426264,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426264,"clinical_significance":[],"seq_region_name":"7","id":"rs2130177233"},{"seq_region_name":"7","id":"rs1209124149","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","CC"],"end":140426266,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426266,"source":"dbSNP"},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426271,"feature_type":"variation","strand":1,"end":140426271,"alleles":["C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130177258"},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426281,"feature_type":"variation","strand":1,"end":140426281,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799671318"},{"alleles":["A","G"],"end":140426282,"feature_type":"variation","strand":1,"source":"dbSNP","start":140426282,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799671380","seq_region_name":"7"},{"end":140426287,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140426287,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130177283"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799671426","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426288,"feature_type":"variation","strand":1,"end":140426288,"alleles":["G","C"]},{"clinical_significance":[],"id":"rs1799671476","seq_region_name":"7","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426289,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140426289},{"start":140426291,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["G","A"],"end":140426291,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1438213709","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140426292,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426292,"clinical_significance":[],"seq_region_name":"7","id":"rs999920372"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140426295,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426295,"clinical_significance":[],"seq_region_name":"7","id":"rs1003020267"},{"seq_region_name":"7","id":"rs1031343080","clinical_significance":[],"start":140426295,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140426299,"alleles":["CACAC","CAC"],"strand":1,"feature_type":"variation"},{"start":140426296,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140426296,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs891638259","clinical_significance":[]},{"end":140426298,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140426298,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs550098913"},{"start":140426299,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["C","A"],"end":140426299,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130177392","clinical_significance":[]},{"alleles":["C","G"],"end":140426302,"feature_type":"variation","strand":1,"source":"dbSNP","start":140426302,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799671819"},{"seq_region_name":"7","id":"rs1315806037","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426305,"source":"dbSNP","strand":1,"feature_type":"variation","end":140426305,"alleles":["C","G"]},{"end":140426315,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140426315,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs1799671913","clinical_significance":[]},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426322,"feature_type":"variation","strand":1,"end":140426322,"alleles":["G","A","C"],"clinical_significance":[],"id":"rs1248331495","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140426324,"alleles":["T","G"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426324,"clinical_significance":[],"seq_region_name":"7","id":"rs1377215690"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130177461","end":140426326,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140426326,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1799672057","clinical_significance":[],"end":140426334,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140426334,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"end":140426337,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140426337,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799672104"},{"feature_type":"variation","strand":1,"end":140426341,"alleles":["C","A"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426341,"clinical_significance":[],"seq_region_name":"7","id":"rs1283857191"},{"source":"dbSNP","start":140426342,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140426342,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799672180"},{"id":"rs1473641586","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426346,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140426346},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426347,"source":"dbSNP","strand":1,"feature_type":"variation","end":140426347,"alleles":["A","T"],"seq_region_name":"7","id":"rs1799672283","clinical_significance":[]},{"source":"dbSNP","start":140426352,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140426352,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799672323","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1799672365","seq_region_name":"7","feature_type":"variation","strand":1,"end":140426355,"alleles":["C","G"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426355},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426358,"feature_type":"variation","strand":1,"end":140426358,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1165263540"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140426359,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426359,"clinical_significance":[],"seq_region_name":"7","id":"rs568249399"},{"source":"dbSNP","start":140426360,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140426360,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799672519"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140426365,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426365,"source":"dbSNP","seq_region_name":"7","id":"rs1799672560","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799672608","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140426367,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426367},{"id":"rs2130177608","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140426373,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426373,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426375,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","G"],"end":140426375,"seq_region_name":"7","id":"rs1014537494","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799672740","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426381,"source":"dbSNP","strand":1,"feature_type":"variation","end":140426381,"alleles":["C","T"]},{"start":140426384,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140426384,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1404867398","clinical_significance":[]},{"id":"rs1034901028","seq_region_name":"7","clinical_significance":[],"start":140426388,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140426388,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140426390,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426390,"clinical_significance":[],"seq_region_name":"7","id":"rs1799672900"},{"alleles":["C","G"],"end":140426391,"strand":1,"feature_type":"variation","start":140426391,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","id":"rs114713232","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs769164342","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426396,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140426396},{"feature_type":"variation","strand":1,"end":140426400,"alleles":["A","G"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426400,"clinical_significance":[],"id":"rs1799673058","seq_region_name":"7"},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426405,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140426405,"clinical_significance":[],"seq_region_name":"7","id":"rs1163640928"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1425080375","source":"dbSNP","start":140426407,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140426407,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1799673220","seq_region_name":"7","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426415,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140426415},{"start":140426416,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["G","T"],"end":140426416,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799673271","clinical_significance":[]},{"clinical_significance":[],"id":"rs974691436","seq_region_name":"7","end":140426418,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140426418,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1180945450","alleles":["G","A"],"end":140426419,"feature_type":"variation","strand":1,"source":"dbSNP","start":140426419,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"start":140426420,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140426420,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130177789","clinical_significance":[]},{"alleles":["A","C"],"end":140426421,"feature_type":"variation","strand":1,"source":"dbSNP","start":140426421,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799673427"},{"start":140426424,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["G","A"],"end":140426424,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs920186837","clinical_significance":[]},{"end":140426429,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140426429,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799673545","seq_region_name":"7"},{"seq_region_name":"7","id":"rs2130177836","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426431,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140426431},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563076619","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426433,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140426433},{"source":"dbSNP","start":140426434,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140426434,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130177863"},{"strand":1,"feature_type":"variation","end":140426436,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426436,"source":"dbSNP","id":"rs371872290","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426444,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TTTT","TTT"],"end":140426447,"seq_region_name":"7","id":"rs1234393006","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799673729","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426445,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140426445},{"clinical_significance":[],"seq_region_name":"7","id":"rs1179822762","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426445,"feature_type":"variation","strand":1,"alleles":["TTTCTGT","T"],"end":140426451},{"feature_type":"variation","strand":1,"end":140426453,"alleles":["T","-"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426453,"clinical_significance":[],"seq_region_name":"7","id":"rs1799673827"},{"clinical_significance":[],"id":"rs1482675808","seq_region_name":"7","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426455,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140426455},{"strand":1,"feature_type":"variation","end":140426456,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426456,"source":"dbSNP","seq_region_name":"7","id":"rs1292465658","clinical_significance":[]},{"alleles":["T","C"],"end":140426457,"feature_type":"variation","strand":1,"source":"dbSNP","start":140426457,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130177949"},{"end":140426460,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140426460,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs2130177961","clinical_significance":[]},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426464,"feature_type":"variation","strand":1,"end":140426464,"alleles":["T","C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1408609808"},{"seq_region_name":"7","id":"rs1343204338","clinical_significance":[],"strand":1,"feature_type":"variation","end":140426470,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426470,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799674091","source":"dbSNP","start":140426472,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140426472,"alleles":["T","C"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140426477,"alleles":["A","G"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426477,"clinical_significance":[],"seq_region_name":"7","id":"rs1799674141"},{"clinical_significance":[],"seq_region_name":"7","id":"rs371039248","end":140426483,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140426483,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"id":"rs1027676267","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426485,"source":"dbSNP","strand":1,"feature_type":"variation","end":140426485,"alleles":["T","C","G"]},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426488,"source":"dbSNP","strand":1,"feature_type":"variation","end":140426488,"alleles":["T","C"],"seq_region_name":"7","id":"rs1799674299","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799674341","clinical_significance":[],"start":140426492,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140426493,"alleles":["TT","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1453880303","source":"dbSNP","start":140426493,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140426493,"alleles":["T","C"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140426502,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426502,"source":"dbSNP","id":"rs1799674428","seq_region_name":"7","clinical_significance":[]},{"end":140426511,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140426511,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs951989385","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140426513,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426513,"clinical_significance":[],"seq_region_name":"7","id":"rs951058494"},{"end":140426516,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140426516,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","id":"rs1799674559","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","C"],"end":140426520,"strand":1,"feature_type":"variation","start":140426520,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","id":"rs1341498342","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140426522,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140426522,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs982429395","seq_region_name":"7"},{"end":140426529,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140426529,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799674677","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140426531,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426531,"clinical_significance":[],"seq_region_name":"7","id":"rs1409652034"},{"alleles":["AAAA","AAAAAA"],"end":140426534,"strand":1,"feature_type":"variation","start":140426531,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","id":"rs1286830981","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140426532,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426532,"source":"dbSNP","seq_region_name":"7","id":"rs2130178208","clinical_significance":[]},{"seq_region_name":"7","id":"rs1346661144","clinical_significance":[],"alleles":["C","G"],"end":140426535,"strand":1,"feature_type":"variation","start":140426535,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"alleles":["AGAGAGAGA","AGAGAGAGAGA"],"end":140426548,"strand":1,"feature_type":"variation","start":140426540,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","id":"rs983545937","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140426542,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140426542,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs912336431"},{"seq_region_name":"7","id":"rs1585438231","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426543,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140426543},{"feature_type":"variation","strand":1,"end":140426550,"alleles":["G","A"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426550,"clinical_significance":[],"seq_region_name":"7","id":"rs1458949085"},{"clinical_significance":[],"id":"rs1347617898","seq_region_name":"7","source":"dbSNP","start":140426552,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140426552,"alleles":["G","A"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426572,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AACAGTTTGAAACAG","AACAG"],"end":140426586,"seq_region_name":"7","id":"rs1799675120","clinical_significance":[]},{"alleles":["A","G"],"end":140426573,"strand":1,"feature_type":"variation","start":140426573,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs1799675174","clinical_significance":[]},{"seq_region_name":"7","id":"rs943744877","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426575,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140426575},{"source":"dbSNP","start":140426586,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140426586,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799675259"},{"seq_region_name":"7","id":"rs1799675303","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426592,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140426592},{"source":"dbSNP","start":140426593,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140426593,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs190069238","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1400917354","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426599,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140426599},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426607,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140426607,"clinical_significance":[],"seq_region_name":"7","id":"rs541799451"},{"end":140426608,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140426608,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1282089053"},{"seq_region_name":"7","id":"rs1269453769","clinical_significance":[],"start":140426617,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140426617,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426618,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140426618,"seq_region_name":"7","id":"rs1563076673","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799675705","alleles":["G","A"],"end":140426621,"feature_type":"variation","strand":1,"source":"dbSNP","start":140426621,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs922108923","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426628,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140426628},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140426630,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426630,"clinical_significance":[],"id":"rs1487506847","seq_region_name":"7"},{"id":"rs1246193166","seq_region_name":"7","clinical_significance":[],"start":140426632,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140426632,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs921064773","seq_region_name":"7","alleles":["T","C"],"end":140426636,"feature_type":"variation","strand":1,"source":"dbSNP","start":140426636,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140426637,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426637,"source":"dbSNP","seq_region_name":"7","id":"rs1563076689","clinical_significance":[]},{"alleles":["A","C","G"],"end":140426640,"feature_type":"variation","strand":1,"source":"dbSNP","start":140426640,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs148788288"},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426651,"feature_type":"variation","strand":1,"end":140426651,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1228500995"},{"seq_region_name":"7","id":"rs1585438336","clinical_significance":[],"strand":1,"feature_type":"variation","end":140426654,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426654,"source":"dbSNP"},{"source":"dbSNP","start":140426656,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140426656,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799676113"},{"alleles":["A","T"],"end":140426657,"strand":1,"feature_type":"variation","start":140426657,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs1318932143","clinical_significance":[]},{"seq_region_name":"7","id":"rs1043957828","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140426658,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426658,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1228122756","clinical_significance":[],"alleles":["C","T"],"end":140426662,"strand":1,"feature_type":"variation","start":140426662,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140426663,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426663,"source":"dbSNP","id":"rs1799676341","seq_region_name":"7","clinical_significance":[]},{"start":140426664,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140426664,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1324743235","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799676453","clinical_significance":[],"alleles":["A","G"],"end":140426668,"strand":1,"feature_type":"variation","start":140426668,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"seq_region_name":"7","id":"rs1799676508","clinical_significance":[],"end":140426670,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140426670,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"start":140426679,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140426679,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs1285678410","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799676610","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140426683,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426683},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140426684,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426684,"source":"dbSNP","id":"rs1385590861","seq_region_name":"7","clinical_significance":[]},{"end":140426686,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140426686,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799676710"},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426687,"source":"dbSNP","strand":1,"feature_type":"variation","end":140426687,"alleles":["C","T"],"seq_region_name":"7","id":"rs539953457","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs563241318","source":"dbSNP","start":140426688,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140426688,"alleles":["G","A"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140426690,"alleles":["A","C"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426690,"clinical_significance":[],"seq_region_name":"7","id":"rs1256730258"},{"start":140426692,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140426692,"alleles":["C","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799676936","clinical_significance":[]},{"seq_region_name":"7","id":"rs1010222660","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140426693,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426693,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140426694,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426694,"source":"dbSNP","seq_region_name":"7","id":"rs891584624","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140426697,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426697,"source":"dbSNP","seq_region_name":"7","id":"rs1456457673","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1041683987","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426700,"feature_type":"variation","strand":1,"end":140426700,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs907317329","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140426705,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426705},{"clinical_significance":[],"seq_region_name":"7","id":"rs1045989257","alleles":["T","A"],"end":140426706,"feature_type":"variation","strand":1,"source":"dbSNP","start":140426706,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs11765962","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426707,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140426707},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140426710,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426710,"source":"dbSNP","id":"rs1001860803","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426712,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140426712,"id":"rs1799677740","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140426714,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426714,"clinical_significance":[],"seq_region_name":"7","id":"rs1392168222"},{"seq_region_name":"7","id":"rs1187151132","clinical_significance":[],"end":140426717,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140426717,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"end":140426719,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140426719,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130178865"},{"seq_region_name":"7","id":"rs866230560","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140426726,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426726,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1427880346","seq_region_name":"7","end":140426727,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140426727,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs959167690","seq_region_name":"7","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426733,"feature_type":"variation","strand":1,"end":140426733,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130178903","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426734,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140426734},{"clinical_significance":[],"id":"rs76614850","seq_region_name":"7","feature_type":"variation","strand":1,"end":140426739,"alleles":["A","G"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426739},{"end":140426742,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140426742,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs1563076751","clinical_significance":[]},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426746,"feature_type":"variation","strand":1,"end":140426746,"alleles":["G","A"],"clinical_significance":[],"id":"rs995679156","seq_region_name":"7"},{"id":"rs1246367807","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140426749,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426749,"source":"dbSNP"},{"end":140426752,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140426752,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799678183"},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426754,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140426754,"clinical_significance":[],"seq_region_name":"7","id":"rs1168543040"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1403469850","source":"dbSNP","start":140426755,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140426755,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs142469886","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426757,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140426757},{"seq_region_name":"7","id":"rs1332530272","clinical_significance":[],"strand":1,"feature_type":"variation","end":140426759,"alleles":["C","A","G"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426759,"source":"dbSNP"},{"source":"dbSNP","start":140426762,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140426762,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1004927536"},{"clinical_significance":[],"seq_region_name":"7","id":"rs951588880","end":140426767,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140426767,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1799678544","clinical_significance":[],"end":140426769,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140426769,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"alleles":["CTCT","CT"],"end":140426772,"strand":1,"feature_type":"variation","start":140426769,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs1799678594","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs982460763","source":"dbSNP","start":140426776,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140426776,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1340240486","feature_type":"variation","strand":1,"end":140426789,"alleles":["C","G"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426789},{"end":140426793,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140426793,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","id":"rs1799678741","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426794,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140426794,"clinical_significance":[],"seq_region_name":"7","id":"rs1585438489"},{"feature_type":"variation","strand":1,"end":140426795,"alleles":["C","T"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426795,"clinical_significance":[],"seq_region_name":"7","id":"rs1435429749"},{"seq_region_name":"7","id":"rs1585438501","clinical_significance":[],"end":140426796,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140426796,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"strand":1,"feature_type":"variation","end":140426797,"alleles":["C","A","G","T"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426797,"source":"dbSNP","seq_region_name":"7","id":"rs1299325521","clinical_significance":[]},{"clinical_significance":[],"id":"rs537341278","seq_region_name":"7","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426798,"feature_type":"variation","strand":1,"end":140426798,"alleles":["C","A"]},{"start":140426799,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140426799,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs965133497","clinical_significance":[]},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426800,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140426800,"clinical_significance":[],"id":"rs975531166","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426801,"source":"dbSNP","strand":1,"feature_type":"variation","end":140426801,"alleles":["C","T"],"seq_region_name":"7","id":"rs183155091","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140426802,"alleles":["T","A","C"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426802,"clinical_significance":[],"seq_region_name":"7","id":"rs4725696"},{"id":"rs1799679402","seq_region_name":"7","clinical_significance":[],"start":140426802,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140426805,"alleles":["TTGG","TTGGTTGG"],"strand":1,"feature_type":"variation"},{"end":140426805,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140426805,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs796523984","clinical_significance":[]},{"alleles":["G","C"],"end":140426806,"feature_type":"variation","strand":1,"source":"dbSNP","start":140426806,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799679546","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140426808,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426808,"source":"dbSNP","seq_region_name":"7","id":"rs1198522930","clinical_significance":[]},{"seq_region_name":"7","id":"rs1376957965","clinical_significance":[],"start":140426811,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140426811,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140426815,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140426815,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799679643"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585438566","alleles":["A","C"],"end":140426817,"feature_type":"variation","strand":1,"source":"dbSNP","start":140426817,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130179304","feature_type":"variation","strand":1,"end":140426818,"alleles":["C","T"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426818},{"start":140426819,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140426819,"alleles":["A","C"],"strand":1,"feature_type":"variation","id":"rs1585438574","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426821,"feature_type":"variation","strand":1,"end":140426821,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1171083956"},{"clinical_significance":[],"seq_region_name":"7","id":"rs186888389","feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140426822,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426822},{"clinical_significance":[],"seq_region_name":"7","id":"rs559537407","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426824,"feature_type":"variation","strand":1,"end":140426824,"alleles":["C","A"]},{"id":"rs62490411","seq_region_name":"7","clinical_significance":[],"start":140426827,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140426827,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs35212469","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["TTTTTTTT","TTTTTTT"],"end":140426834,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426827},{"seq_region_name":"7","id":"rs945273115","clinical_significance":[],"alleles":["T","A","C"],"end":140426828,"strand":1,"feature_type":"variation","start":140426828,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140426829,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426829,"source":"dbSNP","seq_region_name":"7","id":"rs1799680207","clinical_significance":[]},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426829,"feature_type":"variation","strand":1,"alleles":["TTTTTTCTTTCTTTTTT","TTTTTT"],"end":140426845,"clinical_significance":[],"id":"rs1799680262","seq_region_name":"7"},{"end":140426831,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140426831,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130179430"},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426831,"feature_type":"variation","strand":1,"end":140426838,"alleles":["TTTTCTTT","TTT"],"clinical_significance":[],"seq_region_name":"7","id":"rs1797754198"},{"strand":1,"feature_type":"variation","end":140426833,"alleles":["TT","TTCTT"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426832,"source":"dbSNP","id":"rs1799680317","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1199054127","alleles":["TTTCTTTCTTT","TTTCTTT","TTTCTTTCTTTCTTT"],"end":140426842,"feature_type":"variation","strand":1,"source":"dbSNP","start":140426832,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140426833,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426833,"source":"dbSNP","seq_region_name":"7","id":"rs1799680457","clinical_significance":[]},{"end":140426834,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140426834,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs1585438623","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs955382147","alleles":["C","T"],"end":140426835,"feature_type":"variation","strand":1,"source":"dbSNP","start":140426835,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"start":140426836,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140426838,"alleles":["TTT","TTTT"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799680628","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426836,"source":"dbSNP","strand":1,"feature_type":"variation","end":140426856,"alleles":["TTTCTTTTTTTTTTTTTTTTT","TTT"],"seq_region_name":"7","id":"rs1252348315","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1207930720","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426837,"feature_type":"variation","strand":1,"alleles":["TTCTT","TT"],"end":140426841},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140426839,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426839,"source":"dbSNP","seq_region_name":"7","id":"rs75501903","clinical_significance":[]},{"end":140426839,"alleles":["C","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140426839,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs370008585"},{"clinical_significance":[],"seq_region_name":"7","id":"rs398067341","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426840,"feature_type":"variation","strand":1,"alleles":["TTTTTTTTTTTTTTTTTTTT","TTTTTTTTT","TTTTTTTTTTTTT","TTTTTTTTTTTTTT","TTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT"],"end":140426859},{"seq_region_name":"7","id":"rs1799681287","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426842,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","TCT"],"end":140426842},{"end":140426842,"alleles":["-","C"],"strand":1,"feature_type":"variation","start":140426843,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","id":"rs1468088899","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140426843,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426843,"clinical_significance":[],"id":"rs1041707142","seq_region_name":"7"},{"end":140426843,"alleles":["-","A"],"strand":1,"feature_type":"variation","start":140426844,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs1799681471","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140426844,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426844,"clinical_significance":[],"seq_region_name":"7","id":"rs1401998923"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799681558","source":"dbSNP","start":140426845,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140426845,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs201080003","clinical_significance":[],"start":140426847,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["-","C","CTATTCAAATATGCTATTTAAAATATGATATGAAAATATA"],"end":140426846,"strand":1,"feature_type":"variation"},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426847,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140426847,"clinical_significance":[],"seq_region_name":"7","id":"rs4725697"},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426848,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140426848,"seq_region_name":"7","id":"rs1362522510","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799681804","alleles":["T","C"],"end":140426849,"feature_type":"variation","strand":1,"source":"dbSNP","start":140426849,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"start":140426851,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["-","C"],"end":140426850,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1370370089","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799682037","seq_region_name":"7","source":"dbSNP","start":140426853,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140426853,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs2130179770","seq_region_name":"7","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426854,"feature_type":"variation","strand":1,"end":140426854,"alleles":["T","TGT"]},{"start":140426859,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["T","G"],"end":140426859,"strand":1,"feature_type":"variation","id":"rs1799682096","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426860,"feature_type":"variation","strand":1,"end":140426860,"alleles":["G","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1433735839"},{"clinical_significance":[],"id":"rs1799682193","seq_region_name":"7","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426860,"feature_type":"variation","strand":1,"end":140426860,"alleles":["G","GG"]},{"id":"rs1799682237","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426860,"source":"dbSNP","strand":1,"feature_type":"variation","end":140426860,"alleles":["G","-"]},{"end":140426861,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140426861,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1301280374","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799682320","feature_type":"variation","strand":1,"end":140426861,"alleles":["A","-"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426861},{"source":"dbSNP","start":140426862,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140426862,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs2130179848","seq_region_name":"7"},{"start":140426865,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["AG","-"],"end":140426866,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1423538345","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["TACTCTGT","TACTCTGTACTCTGT"],"end":140426879,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426872,"clinical_significance":[],"seq_region_name":"7","id":"rs1251687164"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140426873,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426873,"clinical_significance":[],"seq_region_name":"7","id":"rs1184853294"},{"feature_type":"variation","strand":1,"end":140426874,"alleles":["C","A"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426874,"clinical_significance":[],"seq_region_name":"7","id":"rs2130179905"},{"seq_region_name":"7","id":"rs1799682493","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C","T"],"end":140426878,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426878,"source":"dbSNP"},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426883,"feature_type":"variation","strand":1,"end":140426883,"alleles":["C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799682538"},{"feature_type":"variation","strand":1,"end":140426884,"alleles":["C","T"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426884,"clinical_significance":[],"seq_region_name":"7","id":"rs935582069"},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426885,"feature_type":"variation","strand":1,"end":140426885,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799682634"},{"feature_type":"variation","strand":1,"end":140426890,"alleles":["G","A"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426890,"clinical_significance":[],"seq_region_name":"7","id":"rs1799682665"},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426892,"feature_type":"variation","strand":1,"end":140426892,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585438777"},{"seq_region_name":"7","id":"rs1799682718","clinical_significance":[],"strand":1,"feature_type":"variation","end":140426895,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426895,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1332318717","feature_type":"variation","strand":1,"end":140426896,"alleles":["T","C"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426896},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799682782","source":"dbSNP","start":140426899,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140426912,"alleles":["TGGTGGGATCTTGG","TGG"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1274600476","end":140426905,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140426905,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1585438785","clinical_significance":[],"alleles":["A","G"],"end":140426906,"strand":1,"feature_type":"variation","start":140426906,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1203757739","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426909,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140426909},{"source":"dbSNP","start":140426912,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140426912,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs938691857"},{"strand":1,"feature_type":"variation","end":140426918,"alleles":["CTCACT","CT"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426913,"source":"dbSNP","id":"rs1255319628","seq_region_name":"7","clinical_significance":[]},{"id":"rs1799682993","seq_region_name":"7","clinical_significance":[],"start":140426914,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["-","CCA"],"end":140426913,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1799683021","seq_region_name":"7","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426914,"feature_type":"variation","strand":1,"end":140426914,"alleles":["T","A","C"]},{"alleles":["C","T"],"end":140426917,"strand":1,"feature_type":"variation","start":140426917,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","id":"rs1056314868","seq_region_name":"7","clinical_significance":[]},{"id":"rs1266784780","seq_region_name":"7","clinical_significance":[],"end":140426919,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140426919,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"strand":1,"feature_type":"variation","end":140426920,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426920,"source":"dbSNP","seq_region_name":"7","id":"rs1242167237","clinical_significance":[]},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426923,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140426923,"clinical_significance":[],"id":"rs1585438811","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426927,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140426927,"id":"rs1799683163","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","C","T"],"end":140426928,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426928,"source":"dbSNP","id":"rs1585438824","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585438831","end":140426935,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140426935,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426940,"feature_type":"variation","strand":1,"end":140426940,"alleles":["C","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1339572754"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140426942,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426942,"source":"dbSNP","id":"rs1288723383","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140426944,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140426944,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1411473013"},{"start":140426946,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140426946,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799683368","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1052749942","source":"dbSNP","start":140426948,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140426948,"alleles":["T","A"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140426952,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140426952,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1463657853"},{"source":"dbSNP","start":140426954,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140426954,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585438853"},{"clinical_significance":[],"seq_region_name":"7","id":"rs894546571","feature_type":"variation","strand":1,"end":140426958,"alleles":["C","G","T"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426958},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426959,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140426959,"seq_region_name":"7","id":"rs912871061","clinical_significance":[]},{"end":140426963,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140426963,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1268210394"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799683521","feature_type":"variation","strand":1,"end":140426964,"alleles":["C","T"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426964},{"end":140426966,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140426966,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs571794630"},{"id":"rs1197418507","seq_region_name":"7","clinical_significance":[],"alleles":["A","T"],"end":140426967,"strand":1,"feature_type":"variation","start":140426967,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426968,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140426968,"seq_region_name":"7","id":"rs1799683701","clinical_significance":[]},{"seq_region_name":"7","id":"rs1457587249","clinical_significance":[],"end":140426970,"alleles":["T","C","G"],"strand":1,"feature_type":"variation","start":140426970,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"alleles":["G","A"],"end":140426972,"feature_type":"variation","strand":1,"source":"dbSNP","start":140426972,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799683815"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585438883","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426978,"feature_type":"variation","strand":1,"end":140426978,"alleles":["A","G"]},{"alleles":["G","A"],"end":140426984,"feature_type":"variation","strand":1,"source":"dbSNP","start":140426984,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1027130955"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130180185","end":140426990,"alleles":["ACACAC","AC"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140426985,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140426986,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426986,"source":"dbSNP","id":"rs1799683936","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130180198","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426989,"source":"dbSNP","strand":1,"feature_type":"variation","end":140426989,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs887368905","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426990,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140426990},{"id":"rs1045446481","seq_region_name":"7","clinical_significance":[],"start":140426991,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["G","A"],"end":140426991,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140426992,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140426992,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1471831926","seq_region_name":"7"},{"end":140426993,"alleles":["C","CTGTC"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140426993,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130180221"},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140426995,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140426995,"seq_region_name":"7","id":"rs1799684080","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1251662615","feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140426996,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140426996},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585438915","end":140426997,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140426997,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1200794545","source":"dbSNP","start":140426999,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140426999,"alleles":["T","G"],"feature_type":"variation","strand":1},{"end":140427004,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140427004,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs905702338"},{"strand":1,"feature_type":"variation","end":140427007,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427007,"source":"dbSNP","seq_region_name":"7","id":"rs545914647","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427012,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TT","TTTCTT"],"end":140427013,"seq_region_name":"7","id":"rs2130180269","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799684306","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140427016,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427016},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427017,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TTTTTT","TTTTT","TTTTTTT"],"end":140427022,"id":"rs1001411305","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799684399","alleles":["T","G"],"end":140427020,"feature_type":"variation","strand":1,"source":"dbSNP","start":140427020,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"alleles":["T","C"],"end":140427021,"feature_type":"variation","strand":1,"source":"dbSNP","start":140427021,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1355171072"},{"clinical_significance":[],"id":"rs1268406775","seq_region_name":"7","alleles":["G","A"],"end":140427023,"feature_type":"variation","strand":1,"source":"dbSNP","start":140427023,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"alleles":["A","G"],"end":140427031,"strand":1,"feature_type":"variation","start":140427031,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs563925719","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140427032,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427032,"source":"dbSNP","id":"rs1585438965","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs139467096","alleles":["G","C"],"end":140427033,"feature_type":"variation","strand":1,"source":"dbSNP","start":140427033,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"id":"rs549518414","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427034,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140427034},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427035,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140427035,"clinical_significance":[],"seq_region_name":"7","id":"rs1004788439"},{"source":"dbSNP","start":140427039,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140427039,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1386006556","seq_region_name":"7"},{"end":140427042,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140427042,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs776697393"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140427044,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427044,"clinical_significance":[],"id":"rs966046813","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799684746","source":"dbSNP","start":140427046,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140427046,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs2130180392","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427047,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140427047},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799684773","source":"dbSNP","start":140427052,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140427052,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563076886","end":140427054,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140427054,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140427056,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140427056,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1293739361"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1385890150","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427060,"feature_type":"variation","strand":1,"end":140427060,"alleles":["T","C"]},{"id":"rs1585439029","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427064,"source":"dbSNP","strand":1,"feature_type":"variation","end":140427064,"alleles":["A","C","T"]},{"id":"rs1392318546","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140427065,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427065,"source":"dbSNP"},{"seq_region_name":"7","id":"rs2130180441","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427065,"source":"dbSNP","strand":1,"feature_type":"variation","end":140427069,"alleles":["CTCCT","CT"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1455922057","end":140427066,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140427066,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1411694371","end":140427083,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140427083,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"alleles":["T","G"],"end":140427084,"feature_type":"variation","strand":1,"source":"dbSNP","start":140427084,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799685042"},{"seq_region_name":"7","id":"rs1177686629","clinical_significance":[],"end":140427086,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140427086,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"end":140427088,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140427088,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs1479282026","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140427089,"alleles":["A","C"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427089,"clinical_significance":[],"seq_region_name":"7","id":"rs1585439054"},{"id":"rs1799685174","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427091,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140427091},{"seq_region_name":"7","id":"rs1384537054","clinical_significance":[],"start":140427091,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140427093,"alleles":["CTT","CTTCTT"],"strand":1,"feature_type":"variation"},{"alleles":["T","C"],"end":140427092,"strand":1,"feature_type":"variation","start":140427092,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs2130180493","clinical_significance":[]},{"end":140427093,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140427093,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130180499"},{"end":140427094,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140427094,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1300547804","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427096,"source":"dbSNP","strand":1,"feature_type":"variation","end":140427096,"alleles":["C","T"],"seq_region_name":"7","id":"rs998008833","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799685292","clinical_significance":[],"alleles":["T","C","G"],"end":140427097,"strand":1,"feature_type":"variation","start":140427097,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140427099,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427099,"clinical_significance":[],"seq_region_name":"7","id":"rs1585439076"},{"seq_region_name":"7","id":"rs1799685358","clinical_significance":[],"alleles":["C","A"],"end":140427100,"strand":1,"feature_type":"variation","start":140427100,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427106,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140427106,"clinical_significance":[],"id":"rs1799685391","seq_region_name":"7"},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427107,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140427107,"clinical_significance":[],"id":"rs1376474743","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140427113,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427113,"source":"dbSNP","seq_region_name":"7","id":"rs1799685453","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799685476","clinical_significance":[],"strand":1,"feature_type":"variation","end":140427125,"alleles":["AGGCATGA","AGGCATGAAGGCATGA"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427118,"source":"dbSNP"},{"start":140427121,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140427121,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130180580","clinical_significance":[]},{"alleles":["A","G"],"end":140427122,"strand":1,"feature_type":"variation","start":140427122,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","id":"rs1799685519","seq_region_name":"7","clinical_significance":[]},{"start":140427124,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["G","A","C"],"end":140427124,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1029043738","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130180605","clinical_significance":[],"start":140427126,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140427126,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427127,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140427127,"seq_region_name":"7","id":"rs1230005268","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs964132151","alleles":["A","C"],"end":140427129,"feature_type":"variation","strand":1,"source":"dbSNP","start":140427129,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"alleles":["C","A","T"],"end":140427130,"feature_type":"variation","strand":1,"source":"dbSNP","start":140427130,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799685662","seq_region_name":"7"},{"alleles":["A","C"],"end":140427132,"strand":1,"feature_type":"variation","start":140427132,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs1585439098","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130180649","source":"dbSNP","start":140427132,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["AT","-"],"end":140427133,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1248200430","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427133,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140427133},{"seq_region_name":"7","id":"rs191476809","clinical_significance":[],"end":140427134,"alleles":["G","A","C","T"],"strand":1,"feature_type":"variation","start":140427134,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"seq_region_name":"7","id":"rs1585439111","clinical_significance":[],"start":140427135,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["C","T"],"end":140427135,"strand":1,"feature_type":"variation"},{"end":140427136,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140427136,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130180681"},{"end":140427137,"alleles":["T","C","G"],"strand":1,"feature_type":"variation","start":140427137,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","id":"rs1328210427","seq_region_name":"7","clinical_significance":[]},{"id":"rs1215393089","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140427138,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427138,"source":"dbSNP"},{"id":"rs1799685918","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427138,"source":"dbSNP","strand":1,"feature_type":"variation","end":140427138,"alleles":["G","-"]},{"seq_region_name":"7","id":"rs1799685953","clinical_significance":[],"start":140427138,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140427141,"alleles":["GTTC","-"],"strand":1,"feature_type":"variation"},{"start":140427139,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140427138,"alleles":["-","GCACAAT"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799685996","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140427139,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427139,"source":"dbSNP","seq_region_name":"7","id":"rs1266224982","clinical_significance":[]},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427139,"feature_type":"variation","strand":1,"end":140427140,"alleles":["TT","TTT"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130180743"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1346992874","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427139,"feature_type":"variation","strand":1,"alleles":["TTCTT","TT"],"end":140427143},{"start":140427139,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["TTCTTT","TT"],"end":140427144,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1273035155","clinical_significance":[]},{"start":140427139,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140427146,"alleles":["TTCTTTTT","TT"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1232556090","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140427151,"alleles":["TTCTTTTTTTTTT","TT"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427139,"clinical_significance":[],"seq_region_name":"7","id":"rs1366034628"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1489522437","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427140,"feature_type":"variation","strand":1,"end":140427140,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1322729944","clinical_significance":[],"strand":1,"feature_type":"variation","end":140427142,"alleles":["TCT","T"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427140,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140427141,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427141,"source":"dbSNP","seq_region_name":"7","id":"rs1394545270","clinical_significance":[]},{"source":"dbSNP","start":140427141,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140427141,"alleles":["C","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799686304","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1208084840","feature_type":"variation","strand":1,"end":140427142,"alleles":["T","A","C"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427142},{"seq_region_name":"7","id":"rs34940659","clinical_significance":[],"alleles":["TTTTTTTTTTTTTTTTTTTTT","TTTTTTTT","TTTTTTTTT","TTTTTTTTTTT","TTTTTTTTTTTT","TTTTTTTTTTTTT","TTTTTTTTTTTTTT","TTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTT"],"end":140427162,"strand":1,"feature_type":"variation","start":140427142,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"alleles":["-","A"],"end":140427142,"strand":1,"feature_type":"variation","start":140427143,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs1799686650","clinical_significance":[]},{"seq_region_name":"7","id":"rs1483631472","clinical_significance":[],"end":140427144,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140427144,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"end":140427146,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140427146,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799686715"},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427147,"feature_type":"variation","strand":1,"end":140427146,"alleles":["-","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799686744"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799686778","source":"dbSNP","start":140427147,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140427147,"alleles":["T","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1585439165","clinical_significance":[],"strand":1,"feature_type":"variation","end":140427148,"alleles":["-","C"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427149,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799686828","clinical_significance":[],"strand":1,"feature_type":"variation","end":140427163,"alleles":["TTTTTG","-"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427158,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140427160,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427160,"clinical_significance":[],"seq_region_name":"7","id":"rs1799686853"},{"clinical_significance":[],"id":"rs1799686883","seq_region_name":"7","alleles":["TTTG","-"],"end":140427163,"feature_type":"variation","strand":1,"source":"dbSNP","start":140427160,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427161,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TTG","-"],"end":140427163,"seq_region_name":"7","id":"rs1184968734","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799686950","end":140427163,"alleles":["TG","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140427162,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["G","-"],"end":140427163,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427163,"source":"dbSNP","seq_region_name":"7","id":"rs1299901932","clinical_significance":[]},{"start":140427163,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["G","A","C","T"],"end":140427163,"strand":1,"feature_type":"variation","id":"rs1410292583","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140427164,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427164,"source":"dbSNP","id":"rs1418839247","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1165093167","clinical_significance":[],"strand":1,"feature_type":"variation","end":140427165,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427165,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1585439194","seq_region_name":"7","alleles":["A","T"],"end":140427166,"feature_type":"variation","strand":1,"source":"dbSNP","start":140427166,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs759609136","seq_region_name":"7","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427167,"feature_type":"variation","strand":1,"end":140427167,"alleles":["C","A"]},{"seq_region_name":"7","id":"rs1369800650","clinical_significance":[],"start":140427168,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["T","C","G"],"end":140427168,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1430942940","clinical_significance":[],"strand":1,"feature_type":"variation","end":140427169,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427169,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140427170,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427170,"clinical_significance":[],"id":"rs1799687281","seq_region_name":"7"},{"alleles":["C","T"],"end":140427175,"feature_type":"variation","strand":1,"source":"dbSNP","start":140427175,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799687308","seq_region_name":"7"},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427177,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140427177,"clinical_significance":[],"id":"rs529222981","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799687361","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427178,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140427178},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799687408","end":140427180,"alleles":["T","TT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140427180,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1455944318","clinical_significance":[],"strand":1,"feature_type":"variation","end":140427181,"alleles":["G","C","T"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427181,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427183,"source":"dbSNP","strand":1,"feature_type":"variation","end":140427183,"alleles":["C","T"],"id":"rs1799687469","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1169909380","seq_region_name":"7","source":"dbSNP","start":140427185,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140427185,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs371371639","end":140427189,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140427189,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1418286946","end":140427194,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140427194,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"start":140427196,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140427196,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799687591","clinical_significance":[]},{"start":140427200,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140427200,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130181126","clinical_significance":[]},{"id":"rs1182096962","seq_region_name":"7","clinical_significance":[],"end":140427201,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140427201,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140427208,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427208,"source":"dbSNP","seq_region_name":"7","id":"rs1799687647","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1370631434","feature_type":"variation","strand":1,"end":140427211,"alleles":["C","G"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427211},{"end":140427213,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140427213,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs1235516794","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140427214,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427214,"clinical_significance":[],"seq_region_name":"7","id":"rs1186646021"},{"seq_region_name":"7","id":"rs113959218","clinical_significance":[],"start":140427216,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140427216,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140427220,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140427220,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1276729317","seq_region_name":"7"},{"id":"rs1799687860","seq_region_name":"7","clinical_significance":[],"start":140427223,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["C","A"],"end":140427223,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1799687886","seq_region_name":"7","alleles":["C","A"],"end":140427229,"feature_type":"variation","strand":1,"source":"dbSNP","start":140427229,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1585439249","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427231,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140427231},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799687931","end":140427234,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140427234,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"id":"rs775760631","seq_region_name":"7","clinical_significance":[],"end":140427235,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140427235,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"seq_region_name":"7","id":"rs1585439253","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C","T"],"end":140427237,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427237,"source":"dbSNP"},{"alleles":["T","C"],"end":140427243,"strand":1,"feature_type":"variation","start":140427243,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","id":"rs1799688019","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427245,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140427245,"id":"rs975098360","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140427246,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427246,"source":"dbSNP","seq_region_name":"7","id":"rs1203049397","clinical_significance":[]},{"seq_region_name":"7","id":"rs1028522149","clinical_significance":[],"end":140427248,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140427248,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140427250,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427250,"source":"dbSNP","seq_region_name":"7","id":"rs1799688135","clinical_significance":[]},{"source":"dbSNP","start":140427253,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140427253,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1306079444"},{"id":"rs1799688206","seq_region_name":"7","clinical_significance":[],"start":140427254,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["A","G"],"end":140427254,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140427255,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427255,"source":"dbSNP","seq_region_name":"7","id":"rs1799688238","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799688269","clinical_significance":[],"strand":1,"feature_type":"variation","end":140427258,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427258,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799688300","clinical_significance":[],"start":140427258,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140427262,"alleles":["CTCCT","CT"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs957795403","clinical_significance":[],"start":140427264,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140427264,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"end":140427265,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140427265,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs1228629518","clinical_significance":[]},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427268,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140427268,"clinical_significance":[],"id":"rs1799688416","seq_region_name":"7"},{"end":140427270,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140427270,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs1354589344","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140427271,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427271,"clinical_significance":[],"id":"rs1283954807","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799688491","clinical_significance":[],"alleles":["CCCAAGTAGCTGGG","CCCAAGTAGCTGGGCCCAAGTAGCTGGG"],"end":140427286,"strand":1,"feature_type":"variation","start":140427273,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799688530","end":140427274,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140427274,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs989739476","seq_region_name":"7","end":140427278,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140427278,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1799688580","clinical_significance":[],"start":140427284,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140427284,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427292,"source":"dbSNP","strand":1,"feature_type":"variation","end":140427292,"alleles":["T","C"],"seq_region_name":"7","id":"rs565914787","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799688642","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427294,"source":"dbSNP","strand":1,"feature_type":"variation","end":140427294,"alleles":["G","A"]},{"source":"dbSNP","start":140427295,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140427295,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1323672103"},{"start":140427296,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140427296,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs113454601","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1407384980","source":"dbSNP","start":140427297,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140427297,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs374802815","feature_type":"variation","strand":1,"end":140427300,"alleles":["A","G"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427300},{"seq_region_name":"7","id":"rs1799688808","clinical_significance":[],"end":140427301,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140427301,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130181405","source":"dbSNP","start":140427303,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140427303,"alleles":["A","G"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140427307,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140427307,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs956965759"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1403935010","feature_type":"variation","strand":1,"end":140427308,"alleles":["G","A"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427308},{"clinical_significance":[],"id":"rs1799688904","seq_region_name":"7","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427309,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140427309},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130181434","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427311,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140427311},{"source":"dbSNP","start":140427316,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["C","A","G","T"],"end":140427316,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs12216604"},{"id":"rs1799689232","seq_region_name":"7","clinical_significance":[],"start":140427318,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["TTTTTTTT","TTTTTTTTT"],"end":140427325,"strand":1,"feature_type":"variation"},{"id":"rs1342951234","seq_region_name":"7","clinical_significance":[],"start":140427328,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140427328,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140427330,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140427330,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799689309"},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427338,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140427338,"seq_region_name":"7","id":"rs1411244421","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799689367","clinical_significance":[],"end":140427346,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140427346,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"seq_region_name":"7","id":"rs912892928","clinical_significance":[],"start":140427347,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["T","C"],"end":140427347,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1799689419","clinical_significance":[],"strand":1,"feature_type":"variation","end":140427351,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427351,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140427355,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427355,"source":"dbSNP","id":"rs927875096","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs570062702","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","C","T"],"end":140427356,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427356,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1482727458","seq_region_name":"7","end":140427360,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140427360,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1480530035","seq_region_name":"7","end":140427361,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140427361,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"alleles":["G","C"],"end":140427369,"strand":1,"feature_type":"variation","start":140427369,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs1369425122","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427370,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","TT"],"end":140427370,"id":"rs1799689617","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140427372,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427372,"clinical_significance":[],"seq_region_name":"7","id":"rs1247353672"},{"feature_type":"variation","strand":1,"end":140427373,"alleles":["T","C"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427373,"clinical_significance":[],"id":"rs1182757880","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1223934941","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427374,"source":"dbSNP","strand":1,"feature_type":"variation","end":140427374,"alleles":["G","C"]},{"id":"rs1257842012","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427379,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140427379},{"id":"rs2130181573","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140427381,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427381,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585439379","end":140427383,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140427383,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140427390,"alleles":["G","T"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427390,"clinical_significance":[],"seq_region_name":"7","id":"rs938708074"},{"feature_type":"variation","strand":1,"end":140427392,"alleles":["T","G"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427392,"clinical_significance":[],"id":"rs1799689819","seq_region_name":"7"},{"start":140427395,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["A","C"],"end":140427395,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs977368512","clinical_significance":[]},{"id":"rs1799689871","seq_region_name":"7","clinical_significance":[],"start":140427396,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["C","T"],"end":140427396,"strand":1,"feature_type":"variation"},{"end":140427398,"alleles":["CCC","CC"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140427396,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799689895","seq_region_name":"7"},{"start":140427398,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["C","T"],"end":140427398,"strand":1,"feature_type":"variation","id":"rs1162521503","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1055779972","clinical_significance":[],"strand":1,"feature_type":"variation","end":140427399,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427399,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1331670856","source":"dbSNP","start":140427400,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140427400,"alleles":["T","C"],"feature_type":"variation","strand":1},{"start":140427403,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["C","T"],"end":140427403,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1286926457","clinical_significance":[]},{"source":"dbSNP","start":140427404,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140427404,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs78571503"},{"id":"rs1307942295","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427404,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","GTG"],"end":140427404},{"feature_type":"variation","strand":1,"end":140427404,"alleles":["-","T"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427405,"clinical_significance":[],"id":"rs1799690104","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140427405,"alleles":["G","A"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427405,"clinical_significance":[],"id":"rs1799690124","seq_region_name":"7"},{"clinical_significance":[],"id":"rs555364591","seq_region_name":"7","source":"dbSNP","start":140427406,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140427406,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs573961540","clinical_significance":[],"start":140427411,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["T","C","G"],"end":140427411,"strand":1,"feature_type":"variation"},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427413,"feature_type":"variation","strand":1,"end":140427413,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799690198"},{"id":"rs1799690224","seq_region_name":"7","clinical_significance":[],"alleles":["A","T"],"end":140427414,"strand":1,"feature_type":"variation","start":140427414,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140427415,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427415,"source":"dbSNP","seq_region_name":"7","id":"rs1438037505","clinical_significance":[]},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427418,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140427418,"clinical_significance":[],"seq_region_name":"7","id":"rs1799690269"},{"seq_region_name":"7","id":"rs1353804578","clinical_significance":[],"start":140427431,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140427431,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140427432,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427432,"clinical_significance":[],"seq_region_name":"7","id":"rs1448495935"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140427434,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427434,"clinical_significance":[],"seq_region_name":"7","id":"rs981509914"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799690369","end":140427435,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140427435,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"alleles":["G","A"],"end":140427436,"feature_type":"variation","strand":1,"source":"dbSNP","start":140427436,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1376699539"},{"source":"dbSNP","start":140427437,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140427437,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1457513680"},{"clinical_significance":[],"seq_region_name":"7","id":"rs927105375","source":"dbSNP","start":140427438,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140427438,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140427439,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140427439,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs938347942","seq_region_name":"7"},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427441,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140427441,"clinical_significance":[],"seq_region_name":"7","id":"rs1156759740"},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427442,"source":"dbSNP","strand":1,"feature_type":"variation","end":140427442,"alleles":["A","C"],"id":"rs1799690532","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1418411626","clinical_significance":[],"end":140427443,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140427443,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"source":"dbSNP","start":140427445,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140427445,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799690572"},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140427446,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427446,"source":"dbSNP","seq_region_name":"7","id":"rs1799690595","clinical_significance":[]},{"seq_region_name":"7","id":"rs1450805219","clinical_significance":[],"end":140427447,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140427447,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140427448,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427448,"clinical_significance":[],"seq_region_name":"7","id":"rs1192947545"},{"seq_region_name":"7","id":"rs1799690686","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427449,"source":"dbSNP","strand":1,"feature_type":"variation","end":140427449,"alleles":["G","T"]},{"start":140427450,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140427450,"alleles":["C","A","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1239429124","clinical_significance":[]},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427451,"feature_type":"variation","strand":1,"end":140427451,"alleles":["C","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799690748"},{"seq_region_name":"7","id":"rs937070789","clinical_significance":[],"end":140427452,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140427452,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427453,"source":"dbSNP","strand":1,"feature_type":"variation","end":140427452,"alleles":["-","AA"],"seq_region_name":"7","id":"rs1799690816","clinical_significance":[]},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427453,"feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140427453,"clinical_significance":[],"seq_region_name":"7","id":"rs1208550770"},{"clinical_significance":[],"seq_region_name":"7","id":"rs35384452","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427453,"feature_type":"variation","strand":1,"end":140427468,"alleles":["TTTTTTTTTTTTTTTT","TTTTTTTTTTT","TTTTTTTTTTTT","TTTTTTTTTTTTT","TTTTTTTTTTTTTT","TTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTT"]},{"seq_region_name":"7","id":"rs2130181953","clinical_significance":[],"end":140427454,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","start":140427454,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130181962","end":140427455,"alleles":["-","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140427456,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140427456,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427456,"source":"dbSNP","seq_region_name":"7","id":"rs1799691026","clinical_significance":[]},{"start":140427457,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140427457,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585439453","clinical_significance":[]},{"source":"dbSNP","start":140427458,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140427458,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799691071"},{"seq_region_name":"7","id":"rs1799691102","clinical_significance":[],"start":140427459,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140427459,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1799691127","clinical_significance":[],"start":140427460,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140427460,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"alleles":["-","AGAACCCAAA","AGAACCCAAATCATCTGCCAGATCAGAAGTCA"],"end":140427461,"feature_type":"variation","strand":1,"source":"dbSNP","start":140427462,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130182001"},{"strand":1,"feature_type":"variation","end":140427464,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427464,"source":"dbSNP","seq_region_name":"7","id":"rs1314610388","clinical_significance":[]},{"id":"rs1799691179","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140427468,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427468,"source":"dbSNP"},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427468,"feature_type":"variation","strand":1,"end":140427469,"alleles":["TG","-"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799691203"},{"seq_region_name":"7","id":"rs1289969444","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140427469,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427469,"source":"dbSNP"},{"end":140427469,"alleles":["G","-"],"strand":1,"feature_type":"variation","start":140427469,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs1304090389","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799691294","seq_region_name":"7","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427469,"feature_type":"variation","strand":1,"alleles":["GAGACAGAG","G"],"end":140427477},{"seq_region_name":"7","id":"rs1799691333","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427471,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140427471},{"seq_region_name":"7","id":"rs1364879968","clinical_significance":[],"strand":1,"feature_type":"variation","end":140427472,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427472,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427473,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140427473,"seq_region_name":"7","id":"rs2130182083","clinical_significance":[]},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427474,"feature_type":"variation","strand":1,"end":140427474,"alleles":["A","G"],"clinical_significance":[],"id":"rs1302141585","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140427475,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427475,"source":"dbSNP","seq_region_name":"7","id":"rs1799691420","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140427477,"alleles":["G","T"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427477,"clinical_significance":[],"seq_region_name":"7","id":"rs1273134784"},{"feature_type":"variation","strand":1,"end":140427481,"alleles":["C","T"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427481,"clinical_significance":[],"seq_region_name":"7","id":"rs1390442214"},{"clinical_significance":[],"seq_region_name":"7","id":"rs372212155","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427482,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140427482},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799691682","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427485,"feature_type":"variation","strand":1,"end":140427485,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs553131310","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427492,"feature_type":"variation","strand":1,"end":140427492,"alleles":["C","T"]},{"start":140427494,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["C","A","G"],"end":140427494,"strand":1,"feature_type":"variation","id":"rs1048954314","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140427501,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427501,"source":"dbSNP","seq_region_name":"7","id":"rs1585439483","clinical_significance":[]},{"start":140427503,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140427503,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1482468092","clinical_significance":[]},{"id":"rs1585439490","seq_region_name":"7","clinical_significance":[],"start":140427504,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["T","G"],"end":140427504,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1799691867","clinical_significance":[],"alleles":["A","G"],"end":140427507,"strand":1,"feature_type":"variation","start":140427507,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"clinical_significance":[],"id":"rs1394556374","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140427511,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427511},{"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140427512,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427512,"clinical_significance":[],"seq_region_name":"7","id":"rs1189362101"},{"clinical_significance":[],"seq_region_name":"7","id":"rs894569632","feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140427517,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427517},{"seq_region_name":"7","id":"rs1248213794","clinical_significance":[],"alleles":["C","T"],"end":140427520,"strand":1,"feature_type":"variation","start":140427520,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs144114222","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427521,"feature_type":"variation","strand":1,"end":140427521,"alleles":["G","A","C"]},{"clinical_significance":[],"id":"rs1483796499","seq_region_name":"7","source":"dbSNP","start":140427522,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140427522,"alleles":["G","A"],"feature_type":"variation","strand":1},{"start":140427523,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["C","T"],"end":140427523,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799692074","clinical_significance":[]},{"alleles":["C","T"],"end":140427525,"feature_type":"variation","strand":1,"source":"dbSNP","start":140427525,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs931384274","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799692131","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427529,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140427529},{"source":"dbSNP","start":140427530,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140427533,"alleles":["CAAC","CAACAAC"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799692160","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1418718775","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427532,"source":"dbSNP","strand":1,"feature_type":"variation","end":140427532,"alleles":["A","T"]},{"alleles":["C","T"],"end":140427533,"strand":1,"feature_type":"variation","start":140427533,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs1415041166","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427539,"source":"dbSNP","strand":1,"feature_type":"variation","end":140427539,"alleles":["C","T"],"seq_region_name":"7","id":"rs1048603694","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs183743190","alleles":["C","T"],"end":140427540,"feature_type":"variation","strand":1,"source":"dbSNP","start":140427540,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1799692303","clinical_significance":[],"end":140427542,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140427542,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1312177944","end":140427544,"alleles":["CC","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140427543,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140427546,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427546,"clinical_significance":[],"seq_region_name":"7","id":"rs1799692354"},{"seq_region_name":"7","id":"rs1799692385","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427555,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140427555},{"seq_region_name":"7","id":"rs561176161","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427559,"source":"dbSNP","strand":1,"feature_type":"variation","end":140427559,"alleles":["C","A","G"]},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427566,"source":"dbSNP","strand":1,"feature_type":"variation","end":140427566,"alleles":["C","T"],"seq_region_name":"7","id":"rs1019912635","clinical_significance":[]},{"alleles":["A","C","G"],"end":140427570,"feature_type":"variation","strand":1,"source":"dbSNP","start":140427570,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585439537"},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427571,"feature_type":"variation","strand":1,"alleles":["C","A","G"],"end":140427571,"clinical_significance":[],"seq_region_name":"7","id":"rs2885919"},{"start":140427575,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140427575,"alleles":["C","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799692510","clinical_significance":[]},{"id":"rs1799692530","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140427576,"strand":1,"feature_type":"variation","start":140427576,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427580,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140427580,"seq_region_name":"7","id":"rs1585439543","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799692566","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140427583,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427583},{"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140427586,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427586,"source":"dbSNP","seq_region_name":"7","id":"rs377521674","clinical_significance":[]},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427587,"feature_type":"variation","strand":1,"end":140427587,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1027967278"},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427595,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140427595,"clinical_significance":[],"seq_region_name":"7","id":"rs1379631505"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1366143445","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140427596,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427596},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585439560","feature_type":"variation","strand":1,"end":140427597,"alleles":["T","C"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427597},{"clinical_significance":[],"seq_region_name":"7","id":"rs543375934","source":"dbSNP","start":140427599,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140427599,"feature_type":"variation","strand":1},{"end":140427600,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140427600,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs369631769","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs188606297","alleles":["G","A"],"end":140427601,"feature_type":"variation","strand":1,"source":"dbSNP","start":140427601,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"id":"rs1431740251","seq_region_name":"7","clinical_significance":[],"start":140427605,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140427605,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427606,"source":"dbSNP","strand":1,"feature_type":"variation","end":140427606,"alleles":["C","T"],"seq_region_name":"7","id":"rs758355068","clinical_significance":[]},{"id":"rs1799692897","seq_region_name":"7","clinical_significance":[],"start":140427606,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["CACGCCTAGC","C"],"end":140427615,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140427608,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140427608,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs981894686"},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427609,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140427609,"id":"rs149103971","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140427610,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140427610,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1203381334"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1025262319","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427611,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140427611},{"start":140427612,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["T","A"],"end":140427612,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1485611969","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140427613,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427613,"source":"dbSNP","seq_region_name":"7","id":"rs1253203756","clinical_significance":[]},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427617,"feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140427617,"clinical_significance":[],"id":"rs937918504","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140427623,"alleles":["TTTTT","TTTTTT"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427619,"clinical_significance":[],"seq_region_name":"7","id":"rs1563077115"},{"alleles":["G","C"],"end":140427624,"feature_type":"variation","strand":1,"source":"dbSNP","start":140427624,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799693195","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799693221","feature_type":"variation","strand":1,"end":140427625,"alleles":["T","A"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427625},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140427626,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427626,"clinical_significance":[],"id":"rs1563077116","seq_region_name":"7"},{"source":"dbSNP","start":140427632,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140427632,"alleles":["A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs971387546"},{"end":140427635,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140427635,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799693298"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1343691995","end":140427637,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140427637,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140427639,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427639,"source":"dbSNP","seq_region_name":"7","id":"rs1249196400","clinical_significance":[]},{"clinical_significance":[],"id":"rs991911618","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140427641,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427641},{"clinical_significance":[],"seq_region_name":"7","id":"rs915878586","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427643,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140427643},{"clinical_significance":[],"id":"rs1585439597","seq_region_name":"7","end":140427645,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140427645,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs981155580","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427648,"source":"dbSNP","strand":1,"feature_type":"variation","end":140427648,"alleles":["C","T"]},{"end":140427649,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140427649,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1314585336"},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427651,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140427651,"clinical_significance":[],"seq_region_name":"7","id":"rs1394115686"},{"seq_region_name":"7","id":"rs931392814","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427653,"source":"dbSNP","strand":1,"feature_type":"variation","end":140427653,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs926941197","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427654,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140427654},{"seq_region_name":"7","id":"rs1241075035","clinical_significance":[],"start":140427658,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140427658,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs541363281","source":"dbSNP","start":140427659,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140427659,"feature_type":"variation","strand":1},{"id":"rs1799693680","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427662,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140427662},{"clinical_significance":[],"id":"rs1192891586","seq_region_name":"7","feature_type":"variation","strand":1,"end":140427663,"alleles":["G","A"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427663},{"id":"rs1167466163","seq_region_name":"7","clinical_significance":[],"start":140427666,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140427666,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"start":140427668,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["T","G"],"end":140427668,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585439618","clinical_significance":[]},{"id":"rs1458582423","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427671,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140427671},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427672,"feature_type":"variation","strand":1,"end":140427672,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs908620886"},{"seq_region_name":"7","id":"rs1163069738","clinical_significance":[],"end":140427673,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140427673,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799694536","alleles":["A","T"],"end":140427674,"feature_type":"variation","strand":1,"source":"dbSNP","start":140427674,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"start":140427675,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["C","-"],"end":140427675,"strand":1,"feature_type":"variation","id":"rs1799694561","seq_region_name":"7","clinical_significance":[]},{"end":140427676,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140427676,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs940200953","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs780164716","source":"dbSNP","start":140427678,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140427678,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1253087199","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140427680,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427680},{"seq_region_name":"7","id":"rs1184982844","clinical_significance":[],"alleles":["C","A"],"end":140427683,"strand":1,"feature_type":"variation","start":140427683,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427685,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140427685,"clinical_significance":[],"seq_region_name":"7","id":"rs1482401221"},{"clinical_significance":[],"id":"rs1799694761","seq_region_name":"7","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427686,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140427686},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427687,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140427687,"clinical_significance":[],"id":"rs1041218678","seq_region_name":"7"},{"source":"dbSNP","start":140427690,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["T","A","C"],"end":140427690,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs751820691","seq_region_name":"7"},{"start":140427691,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140427691,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs1488586554","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs559583507","alleles":["C","T"],"end":140427692,"feature_type":"variation","strand":1,"source":"dbSNP","start":140427692,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"id":"rs1585439659","seq_region_name":"7","clinical_significance":[],"start":140427693,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["A","C","G"],"end":140427693,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1480002850","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140427694,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427694,"source":"dbSNP"},{"source":"dbSNP","start":140427697,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140427697,"alleles":["G","GGG"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799694969"},{"seq_region_name":"7","id":"rs1799694993","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140427698,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427698,"source":"dbSNP"},{"alleles":["T","-"],"end":140427700,"feature_type":"variation","strand":1,"source":"dbSNP","start":140427700,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799695019"},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427701,"source":"dbSNP","strand":1,"feature_type":"variation","end":140427701,"alleles":["C","T"],"seq_region_name":"7","id":"rs533193713","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427702,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140427702,"seq_region_name":"7","id":"rs1333905189","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130182866","clinical_significance":[],"start":140427707,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["C","T"],"end":140427707,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140427712,"alleles":["A","G"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427712,"clinical_significance":[],"seq_region_name":"7","id":"rs1799695112"},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427713,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140427713,"id":"rs1799695132","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1230137298","clinical_significance":[],"end":140427715,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140427715,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799695189","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427719,"feature_type":"variation","strand":1,"end":140427719,"alleles":["T","G"]},{"seq_region_name":"7","id":"rs940469755","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427720,"source":"dbSNP","strand":1,"feature_type":"variation","end":140427720,"alleles":["G","A"]},{"id":"rs551290272","seq_region_name":"7","clinical_significance":[],"end":140427730,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140427730,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"source":"dbSNP","start":140427731,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140427731,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs901442367"},{"clinical_significance":[],"seq_region_name":"7","id":"rs191041228","source":"dbSNP","start":140427732,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140427732,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140427733,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427733,"source":"dbSNP","seq_region_name":"7","id":"rs1036188533","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1049870379","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427737,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140427737},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427739,"source":"dbSNP","strand":1,"feature_type":"variation","end":140427739,"alleles":["A","G"],"seq_region_name":"7","id":"rs901798375","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140427741,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427741,"source":"dbSNP","seq_region_name":"7","id":"rs893510388","clinical_significance":[]},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427742,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140427742,"clinical_significance":[],"seq_region_name":"7","id":"rs1413162236"},{"start":140427744,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140427744,"alleles":["A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799695535","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427746,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140427746,"seq_region_name":"7","id":"rs1050477389","clinical_significance":[]},{"clinical_significance":[],"id":"rs374064307","seq_region_name":"7","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427750,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140427750},{"alleles":["T","C"],"end":140427752,"strand":1,"feature_type":"variation","start":140427752,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs1363770191","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs889092794","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427752,"feature_type":"variation","strand":1,"end":140427758,"alleles":["TTTTTTT","TTTTTTTT"]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140427755,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427755,"clinical_significance":[],"seq_region_name":"7","id":"rs1799695668"},{"seq_region_name":"7","id":"rs73482590","clinical_significance":[],"start":140427756,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140427756,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1799695735","clinical_significance":[],"end":140427757,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140427757,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427757,"feature_type":"variation","strand":1,"alleles":["TTATTATTATTATT","TTATTATTATT","TTATTATTATTATTATT"],"end":140427770,"clinical_significance":[],"seq_region_name":"7","id":"rs774547832"},{"seq_region_name":"7","id":"rs1020687359","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140427758,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427758,"source":"dbSNP"},{"end":140427759,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140427759,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","id":"rs1211442459","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799695885","clinical_significance":[],"end":140427761,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140427761,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"alleles":["T","C"],"end":140427767,"feature_type":"variation","strand":1,"source":"dbSNP","start":140427767,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1585439707","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140427775,"alleles":["A","T"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427775,"clinical_significance":[],"seq_region_name":"7","id":"rs1467799475"},{"feature_type":"variation","strand":1,"end":140427777,"alleles":["A","T"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427777,"clinical_significance":[],"seq_region_name":"7","id":"rs2130183080"},{"id":"rs892542820","seq_region_name":"7","clinical_significance":[],"start":140427782,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140427782,"alleles":["G","A","T"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140427783,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140427783,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1976852"},{"end":140427784,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140427784,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1348402928"},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427787,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140427787,"seq_region_name":"7","id":"rs1278908506","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1233981106","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427788,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140427788},{"seq_region_name":"7","id":"rs1799696135","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427790,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140427790},{"seq_region_name":"7","id":"rs182276641","clinical_significance":[],"end":140427791,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140427791,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"source":"dbSNP","start":140427792,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140427792,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1003349525"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1440433971","source":"dbSNP","start":140427802,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140427802,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs532016137","clinical_significance":[],"start":140427804,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140427804,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799696290","feature_type":"variation","strand":1,"end":140427806,"alleles":["T","C"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427806},{"end":140427812,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140427812,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs1799696307","clinical_significance":[]},{"source":"dbSNP","start":140427813,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140427813,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799696336"},{"id":"rs1322938027","seq_region_name":"7","clinical_significance":[],"start":140427815,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["C","T"],"end":140427815,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1799696392","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427816,"source":"dbSNP","strand":1,"feature_type":"variation","end":140427816,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1456006983","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427824,"feature_type":"variation","strand":1,"end":140427824,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs754695737","alleles":["A","C"],"end":140427826,"feature_type":"variation","strand":1,"source":"dbSNP","start":140427826,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs74484995","alleles":["G","A","T"],"end":140427828,"feature_type":"variation","strand":1,"source":"dbSNP","start":140427828,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"id":"rs1799696557","seq_region_name":"7","clinical_significance":[],"start":140427836,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["C","T"],"end":140427836,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1799696592","clinical_significance":[],"strand":1,"feature_type":"variation","end":140427845,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427845,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1378846639","clinical_significance":[],"alleles":["T","C"],"end":140427846,"strand":1,"feature_type":"variation","start":140427846,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1191261093","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427847,"feature_type":"variation","strand":1,"end":140427847,"alleles":["C","T"]},{"feature_type":"variation","strand":1,"end":140427849,"alleles":["C","T"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427849,"clinical_significance":[],"seq_region_name":"7","id":"rs920506043"},{"start":140427851,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["AAGT","AAGTAAGT"],"end":140427854,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1331649378","clinical_significance":[]},{"start":140427855,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["G","T"],"end":140427855,"strand":1,"feature_type":"variation","id":"rs1799696721","seq_region_name":"7","clinical_significance":[]},{"start":140427856,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140427856,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1190213069","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799696775","alleles":["G","T"],"end":140427858,"feature_type":"variation","strand":1,"source":"dbSNP","start":140427858,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1585439786","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427870,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140427870},{"seq_region_name":"7","id":"rs1445077726","clinical_significance":[],"end":140427872,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140427872,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"start":140427874,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140427874,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","id":"rs1221763581","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799696894","end":140427906,"alleles":["CATGCCTGGCACAATTTCTTTCTAGAAC","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140427879,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799696920","feature_type":"variation","strand":1,"end":140427882,"alleles":["G","T"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427882},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427883,"source":"dbSNP","strand":1,"feature_type":"variation","end":140427883,"alleles":["C","T"],"seq_region_name":"7","id":"rs1799696937","clinical_significance":[]},{"start":140427890,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140427890,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130183422","clinical_significance":[]},{"seq_region_name":"7","id":"rs1283081738","clinical_significance":[],"end":140427891,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140427891,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"strand":1,"feature_type":"variation","end":140427901,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427901,"source":"dbSNP","id":"rs1799696994","seq_region_name":"7","clinical_significance":[]},{"start":140427902,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140427902,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799697019","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140427904,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427904,"clinical_significance":[],"seq_region_name":"7","id":"rs1200956059"},{"strand":1,"feature_type":"variation","end":140427908,"alleles":["CCC","CCCC"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427906,"source":"dbSNP","seq_region_name":"7","id":"rs146818503","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799697115","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427911,"source":"dbSNP","strand":1,"feature_type":"variation","end":140427911,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1278262150","source":"dbSNP","start":140427930,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140427930,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427931,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140427931,"id":"rs1799697163","seq_region_name":"7","clinical_significance":[]},{"start":140427933,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140427933,"alleles":["A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799697186","clinical_significance":[]},{"clinical_significance":[],"id":"rs1233714918","seq_region_name":"7","source":"dbSNP","start":140427934,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140427934,"feature_type":"variation","strand":1},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427938,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140427938,"clinical_significance":[],"seq_region_name":"7","id":"rs143191311"},{"seq_region_name":"7","id":"rs984109141","clinical_significance":[],"start":140427946,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140427946,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1799697378","clinical_significance":[],"start":140427955,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["G","C"],"end":140427955,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140427956,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427956,"source":"dbSNP","seq_region_name":"7","id":"rs1428993317","clinical_significance":[]},{"seq_region_name":"7","id":"rs1326214274","clinical_significance":[],"end":140427966,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140427966,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140427969,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140427969,"source":"dbSNP","seq_region_name":"7","id":"rs971945226","clinical_significance":[]},{"clinical_significance":[],"id":"rs1416633350","seq_region_name":"7","source":"dbSNP","start":140427971,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140427971,"feature_type":"variation","strand":1},{"alleles":["C","G"],"end":140427977,"strand":1,"feature_type":"variation","start":140427977,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1374215576","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799697950","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140427984,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140427984,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140427987,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140427987,"source":"dbSNP","seq_region_name":"7","id":"rs539173817","clinical_significance":[]},{"end":140427998,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140427998,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1799698021","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140428005,"alleles":["TAAGATA","TAAGATAAGATA"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140427999,"clinical_significance":[],"seq_region_name":"7","id":"rs1433582463"},{"alleles":["A","C"],"end":140428001,"strand":1,"feature_type":"variation","start":140428001,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs2130183602","seq_region_name":"7","clinical_significance":[]},{"start":140428001,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140428013,"alleles":["AGATATGGCCAGA","AGA"],"strand":1,"feature_type":"variation","id":"rs1390340395","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1689979276","alleles":["A","-"],"end":140428003,"feature_type":"variation","strand":1,"source":"dbSNP","start":140428003,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs940065354","clinical_significance":[],"end":140428004,"alleles":["T","C","G"],"strand":1,"feature_type":"variation","start":140428004,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140428006,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428006,"clinical_significance":[],"seq_region_name":"7","id":"rs1585439832"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428010,"feature_type":"variation","strand":1,"end":140428010,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130183655"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428011,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140428011,"clinical_significance":[],"seq_region_name":"7","id":"rs1799698169"},{"clinical_significance":[],"id":"rs1474258890","seq_region_name":"7","source":"dbSNP","start":140428012,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140428012,"alleles":["G","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1799698228","clinical_significance":[],"start":140428014,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140428014,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"id":"rs1799698256","seq_region_name":"7","clinical_significance":[],"end":140428015,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140428015,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1241296633","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140428024,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428024,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1563077223","seq_region_name":"7","feature_type":"variation","strand":1,"end":140428027,"alleles":["CC","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428026},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140428027,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428027,"clinical_significance":[],"seq_region_name":"7","id":"rs1799698339"},{"start":140428027,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140428045,"alleles":["CTTCTGGGATGGAGTAACT","CT"],"strand":1,"feature_type":"variation","id":"rs1799698366","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428030,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140428030,"id":"rs1041249233","seq_region_name":"7","clinical_significance":[]},{"end":140428049,"alleles":["GGGATGGAGTAACTGCGG","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140428032,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs901018515"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799698445","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428039,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140428039},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140428040,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428040,"source":"dbSNP","id":"rs1799698476","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs922762514","clinical_significance":[],"end":140428041,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140428041,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"id":"rs1799698534","seq_region_name":"7","clinical_significance":[],"start":140428042,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140428043,"alleles":["AA","AAA"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799698565","source":"dbSNP","start":140428045,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140428045,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs932808394","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140428047,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428047,"source":"dbSNP"},{"seq_region_name":"7","id":"rs557292325","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140428048,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428048,"source":"dbSNP"},{"seq_region_name":"7","id":"rs2130183820","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140428056,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428056,"source":"dbSNP"},{"seq_region_name":"7","id":"rs779615001","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140428061,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428061,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1407467812","source":"dbSNP","start":140428062,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140428062,"alleles":["A","G"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428066,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140428066,"seq_region_name":"7","id":"rs576051730","clinical_significance":[]},{"start":140428067,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140428067,"strand":1,"feature_type":"variation","id":"rs892577080","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799698798","seq_region_name":"7","source":"dbSNP","start":140428069,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140428069,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140428077,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140428077,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1009594985","seq_region_name":"7"},{"source":"dbSNP","start":140428078,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140428078,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1042012560"},{"strand":1,"feature_type":"variation","end":140428079,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428079,"source":"dbSNP","id":"rs1363781491","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140428080,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428080,"source":"dbSNP","id":"rs1450672493","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799698954","clinical_significance":[],"end":140428084,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140428084,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"id":"rs534379322","seq_region_name":"7","source":"dbSNP","start":140428086,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140428086,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140428091,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140428091,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1046573940"},{"start":140428092,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140428092,"strand":1,"feature_type":"variation","id":"rs1312816967","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428093,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140428093,"seq_region_name":"7","id":"rs543186341","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799699088","source":"dbSNP","start":140428094,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140428094,"feature_type":"variation","strand":1},{"start":140428099,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140428099,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1413556353","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140428100,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428100,"source":"dbSNP","seq_region_name":"7","id":"rs1003211666","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1171970734","source":"dbSNP","start":140428101,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140428101,"feature_type":"variation","strand":1},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428105,"feature_type":"variation","strand":1,"end":140428105,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799699168"},{"feature_type":"variation","strand":1,"end":140428106,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428106,"clinical_significance":[],"seq_region_name":"7","id":"rs1407839243"},{"id":"rs1418406094","seq_region_name":"7","clinical_significance":[],"start":140428117,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140428117,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1163584392","clinical_significance":[],"end":140428120,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140428120,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"source":"dbSNP","start":140428122,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140428122,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799699283"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1473670201","feature_type":"variation","strand":1,"end":140428124,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428124},{"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140428126,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428126,"clinical_significance":[],"seq_region_name":"7","id":"rs1799699344"},{"id":"rs1563077253","seq_region_name":"7","clinical_significance":[],"start":140428130,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140428130,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140428132,"alleles":["C","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428132,"clinical_significance":[],"seq_region_name":"7","id":"rs1585439905"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799699413","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428134,"feature_type":"variation","strand":1,"end":140428134,"alleles":["G","T"]},{"alleles":["C","T"],"end":140428136,"feature_type":"variation","strand":1,"source":"dbSNP","start":140428136,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1415507106"},{"seq_region_name":"7","id":"rs1187144927","clinical_significance":[],"start":140428145,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140428145,"alleles":["C","A","T"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428148,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140428148,"id":"rs1585439913","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799699529","clinical_significance":[],"start":140428150,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140428150,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1483380340","alleles":["C","T"],"end":140428152,"feature_type":"variation","strand":1,"source":"dbSNP","start":140428152,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"alleles":["G","A"],"end":140428153,"strand":1,"feature_type":"variation","start":140428153,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs748808342","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1202571155","end":140428155,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140428155,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs186940271","clinical_significance":[],"end":140428157,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140428157,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"end":140428163,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140428163,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799699692","clinical_significance":[]},{"end":140428167,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140428167,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs114461635","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140428170,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428170,"clinical_significance":[],"id":"rs1799699784","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1440419727","seq_region_name":"7","source":"dbSNP","start":140428171,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140428171,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1799699843","seq_region_name":"7","alleles":["G","A"],"end":140428175,"feature_type":"variation","strand":1,"source":"dbSNP","start":140428175,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"id":"rs1278618551","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428177,"source":"dbSNP","strand":1,"feature_type":"variation","end":140428191,"alleles":["ACTGTGGACACTCAC","AC"]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428181,"source":"dbSNP","strand":1,"feature_type":"variation","end":140428181,"alleles":["T","G"],"seq_region_name":"7","id":"rs1799699898","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428183,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140428183,"id":"rs553024488","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799699975","end":140428187,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140428187,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1333152044","end":140428188,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140428188,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140428190,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140428190,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799700027"},{"source":"dbSNP","start":140428192,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140428192,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130184221"},{"clinical_significance":[],"seq_region_name":"7","id":"rs951925281","end":140428196,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140428196,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428202,"source":"dbSNP","strand":1,"feature_type":"variation","end":140428202,"alleles":["C","T"],"seq_region_name":"7","id":"rs559640068","clinical_significance":[]},{"source":"dbSNP","start":140428203,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140428203,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs533098935"},{"clinical_significance":[],"id":"rs2130184252","seq_region_name":"7","end":140428209,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140428209,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"alleles":["CAAACACCA","CA"],"end":140428217,"feature_type":"variation","strand":1,"source":"dbSNP","start":140428209,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799700153"},{"seq_region_name":"7","id":"rs1799700186","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140428210,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428210,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1799700222","seq_region_name":"7","alleles":["A","C"],"end":140428212,"feature_type":"variation","strand":1,"source":"dbSNP","start":140428212,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799700243","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140428215,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428215},{"clinical_significance":[],"seq_region_name":"7","id":"rs1299357878","end":140428216,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140428216,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"start":140428218,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","G"],"end":140428218,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1439435404","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1353515242","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428222,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140428222},{"alleles":["G","A"],"end":140428223,"feature_type":"variation","strand":1,"source":"dbSNP","start":140428223,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799700342"},{"id":"rs1799700367","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428224,"source":"dbSNP","strand":1,"feature_type":"variation","end":140428224,"alleles":["A","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130184328","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428225,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140428225},{"seq_region_name":"7","id":"rs1799700396","clinical_significance":[],"alleles":["C","G"],"end":140428228,"strand":1,"feature_type":"variation","start":140428228,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"alleles":["A","G"],"end":140428236,"strand":1,"feature_type":"variation","start":140428236,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1205829531","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140428249,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428249,"clinical_significance":[],"id":"rs1799700453","seq_region_name":"7"},{"seq_region_name":"7","id":"rs191722977","clinical_significance":[],"end":140428252,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140428252,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"end":140428254,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140428254,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585439973"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428261,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140428261,"seq_region_name":"7","id":"rs1462760290","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140428266,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428266,"clinical_significance":[],"seq_region_name":"7","id":"rs1799700571"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1435889347","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140428270,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428270},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140428274,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428274,"clinical_significance":[],"seq_region_name":"7","id":"rs1180752939"},{"source":"dbSNP","start":140428275,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140428275,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1232524082"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799700682","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428280,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140428280},{"clinical_significance":[],"seq_region_name":"7","id":"rs563373218","alleles":["G","C"],"end":140428281,"feature_type":"variation","strand":1,"source":"dbSNP","start":140428281,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140428284,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428284,"clinical_significance":[],"id":"rs151246175","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799700774","source":"dbSNP","start":140428285,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140428285,"alleles":["A","G"],"feature_type":"variation","strand":1},{"end":140428287,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140428287,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1410111458"},{"strand":1,"feature_type":"variation","end":140428288,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428288,"source":"dbSNP","seq_region_name":"7","id":"rs2130184469","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799700814","feature_type":"variation","strand":1,"end":140428289,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428289},{"seq_region_name":"7","id":"rs1175504522","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140428293,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428293,"source":"dbSNP"},{"id":"rs549114098","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140428294,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428294,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140428296,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428296,"clinical_significance":[],"seq_region_name":"7","id":"rs115264078"},{"seq_region_name":"7","id":"rs2130184505","clinical_significance":[],"end":140428298,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140428298,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"id":"rs1247438735","seq_region_name":"7","clinical_significance":[],"end":140428302,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140428302,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1563077285","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428304,"source":"dbSNP","strand":1,"feature_type":"variation","end":140428304,"alleles":["T","A"]},{"id":"rs2130184524","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428305,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140428305},{"clinical_significance":[],"seq_region_name":"7","id":"rs1383522420","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428310,"feature_type":"variation","strand":1,"end":140428310,"alleles":["T","C"]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428312,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140428312,"id":"rs1799700973","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799700993","clinical_significance":[],"alleles":["A","G"],"end":140428314,"strand":1,"feature_type":"variation","start":140428314,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"end":140428315,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140428315,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799701013","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428317,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140428317,"seq_region_name":"7","id":"rs1799701045","clinical_significance":[]},{"id":"rs1585440002","seq_region_name":"7","clinical_significance":[],"start":140428319,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140428319,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140428321,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428321,"clinical_significance":[],"seq_region_name":"7","id":"rs1467351517"},{"end":140428323,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140428323,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1272916635","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585440013","source":"dbSNP","start":140428324,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140428324,"alleles":["A","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1209796537","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428328,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140428328},{"seq_region_name":"7","id":"rs1799701202","clinical_significance":[],"strand":1,"feature_type":"variation","end":140428330,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428330,"source":"dbSNP"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428331,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140428331,"clinical_significance":[],"seq_region_name":"7","id":"rs1799701224"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585440018","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140428332,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428332},{"seq_region_name":"7","id":"rs1585440022","clinical_significance":[],"strand":1,"feature_type":"variation","end":140428333,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428333,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1424064388","clinical_significance":[],"start":140428334,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140428334,"alleles":["C","A","T"],"strand":1,"feature_type":"variation"},{"alleles":["C","G","T"],"end":140428339,"feature_type":"variation","strand":1,"source":"dbSNP","start":140428339,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs922669704"},{"clinical_significance":[],"seq_region_name":"7","id":"rs932862511","end":140428340,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140428340,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799701429","alleles":["T","C"],"end":140428343,"feature_type":"variation","strand":1,"source":"dbSNP","start":140428343,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1372900751","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428345,"source":"dbSNP","strand":1,"feature_type":"variation","end":140428345,"alleles":["C","G"]},{"clinical_significance":[],"id":"rs923133415","seq_region_name":"7","feature_type":"variation","strand":1,"end":140428349,"alleles":["T","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428349},{"feature_type":"variation","strand":1,"end":140428350,"alleles":["G","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428350,"clinical_significance":[],"id":"rs747875696","seq_region_name":"7"},{"clinical_significance":[],"id":"rs772068285","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140428351,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428351},{"strand":1,"feature_type":"variation","end":140428353,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428353,"source":"dbSNP","seq_region_name":"7","id":"rs986012272","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140428354,"alleles":["C","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428354,"clinical_significance":[],"seq_region_name":"7","id":"rs1799701624"},{"start":140428355,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140428358,"alleles":["TCTT","T"],"strand":1,"feature_type":"variation","id":"rs1799701649","seq_region_name":"7","clinical_significance":[]},{"id":"rs777676833","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140428356,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428356,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1585440045","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428356,"source":"dbSNP","strand":1,"feature_type":"variation","end":140428356,"alleles":["C","-"]},{"seq_region_name":"7","id":"rs1274998676","clinical_significance":[],"alleles":["-","A"],"end":140428356,"strand":1,"feature_type":"variation","start":140428357,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585440048","source":"dbSNP","start":140428357,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C","G"],"end":140428357,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428357,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TTTTTTTTT","TTTTTTTT","TTTTTTTTTT"],"end":140428365,"seq_region_name":"7","id":"rs10710018","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428365,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140428365,"seq_region_name":"7","id":"rs1799701900","clinical_significance":[]},{"end":140428367,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140428367,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs745999285","clinical_significance":[]},{"source":"dbSNP","start":140428370,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140428370,"alleles":["C","A","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs769884246"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1457592791","source":"dbSNP","start":140428371,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140428371,"feature_type":"variation","strand":1},{"id":"rs775389046","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140428373,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428373,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1346834173","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140428374,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428374},{"id":"rs763256010","seq_region_name":"7","clinical_significance":[],"start":140428378,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140428378,"alleles":["C","G","T"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140428379,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428379,"clinical_significance":[],"seq_region_name":"7","id":"rs1400111071"},{"alleles":["T","C"],"end":140428385,"strand":1,"feature_type":"variation","start":140428385,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs768698500","clinical_significance":[]},{"end":140428388,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140428388,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs528430375","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140428393,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428393,"clinical_significance":[],"id":"rs1799702199","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799702216","end":140428398,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140428398,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1799702234","clinical_significance":[],"strand":1,"feature_type":"variation","end":140428403,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428403,"source":"dbSNP"},{"id":"rs1799702255","seq_region_name":"7","clinical_significance":[],"start":140428405,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140428405,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs910508927","clinical_significance":[],"strand":1,"feature_type":"variation","end":140428406,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428406,"source":"dbSNP"},{"id":"rs936576364","seq_region_name":"7","clinical_significance":[],"start":140428409,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140428409,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1799702352","clinical_significance":[],"start":140428410,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","A"],"end":140428410,"strand":1,"feature_type":"variation"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428416,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140428416,"clinical_significance":[],"seq_region_name":"7","id":"rs1452779745"},{"clinical_significance":[],"seq_region_name":"7","id":"rs946941634","alleles":["C","T"],"end":140428421,"feature_type":"variation","strand":1,"source":"dbSNP","start":140428421,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428422,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140428422,"clinical_significance":[],"id":"rs1189563621","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1487064332","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140428427,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428427,"source":"dbSNP"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428428,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140428428,"clinical_significance":[],"seq_region_name":"7","id":"rs1585440107"},{"source":"dbSNP","start":140428429,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140428429,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1341444855"},{"id":"rs1042043849","seq_region_name":"7","clinical_significance":[],"alleles":["C","A"],"end":140428430,"strand":1,"feature_type":"variation","start":140428430,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"source":"dbSNP","start":140428434,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140428434,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585440114"},{"seq_region_name":"7","id":"rs1215698897","clinical_significance":[],"strand":1,"feature_type":"variation","end":140428435,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428435,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1585440123","clinical_significance":[],"end":140428439,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140428439,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140428441,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428441,"source":"dbSNP","seq_region_name":"7","id":"rs1799702667","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1312418550","feature_type":"variation","strand":1,"end":140428442,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428442},{"end":140428444,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140428444,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs546590487"},{"strand":1,"feature_type":"variation","end":140428450,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428450,"source":"dbSNP","seq_region_name":"7","id":"rs1228424109","clinical_significance":[]},{"seq_region_name":"7","id":"rs184887223","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C","T"],"end":140428465,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428465,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799702773","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140428467,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428467,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1337291696","source":"dbSNP","start":140428472,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140428472,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140428473,"alleles":["G","A","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428473,"clinical_significance":[],"id":"rs557513590","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799702862","clinical_significance":[],"end":140428475,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140428475,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"id":"rs1363806492","seq_region_name":"7","clinical_significance":[],"end":140428483,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140428483,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585440145","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428485,"feature_type":"variation","strand":1,"end":140428485,"alleles":["T","C","G"]},{"id":"rs1286956115","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428488,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140428488},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428489,"feature_type":"variation","strand":1,"end":140428489,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1279135406"},{"clinical_significance":[],"seq_region_name":"7","id":"rs894874632","source":"dbSNP","start":140428490,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140428490,"alleles":["G","A","C"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428491,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140428491,"seq_region_name":"7","id":"rs1799703066","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140428492,"alleles":["G","A","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428492,"clinical_significance":[],"seq_region_name":"7","id":"rs569378161"},{"strand":1,"feature_type":"variation","end":140428493,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428493,"source":"dbSNP","id":"rs906708787","seq_region_name":"7","clinical_significance":[]},{"end":140428494,"alleles":["T","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140428494,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1241486663"},{"id":"rs1585440174","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428494,"source":"dbSNP","strand":1,"feature_type":"variation","end":140428494,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1799703182","clinical_significance":[],"start":140428495,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140428495,"strand":1,"feature_type":"variation"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428496,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140428496,"clinical_significance":[],"seq_region_name":"7","id":"rs75554518"},{"feature_type":"variation","strand":1,"end":140428497,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428497,"clinical_significance":[],"seq_region_name":"7","id":"rs938209765"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1055295068","source":"dbSNP","start":140428500,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140428500,"alleles":["A","G"],"feature_type":"variation","strand":1},{"end":140428501,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140428501,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1430589407"},{"feature_type":"variation","strand":1,"end":140428504,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428504,"clinical_significance":[],"seq_region_name":"7","id":"rs888723656"},{"alleles":["A","T"],"end":140428505,"feature_type":"variation","strand":1,"source":"dbSNP","start":140428505,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799703335"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140428508,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428508,"source":"dbSNP","seq_region_name":"7","id":"rs1799703360","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140428509,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428509,"clinical_significance":[],"id":"rs1799703375","seq_region_name":"7"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428510,"feature_type":"variation","strand":1,"end":140428510,"alleles":["G","A"],"clinical_significance":[],"id":"rs1799703404","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1444108789","seq_region_name":"7","source":"dbSNP","start":140428511,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140428511,"alleles":["A","C"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140428520,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428520,"source":"dbSNP","seq_region_name":"7","id":"rs1799703446","clinical_significance":[]},{"seq_region_name":"7","id":"rs1186352773","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428521,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140428521},{"start":140428527,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","A"],"end":140428527,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799703498","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140428535,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428535,"clinical_significance":[],"seq_region_name":"7","id":"rs1799703526"},{"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140428536,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428536,"clinical_significance":[],"seq_region_name":"7","id":"rs1005792494"},{"seq_region_name":"7","id":"rs1015949545","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428537,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140428537},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428538,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140428538,"seq_region_name":"7","id":"rs1189238231","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428539,"source":"dbSNP","strand":1,"feature_type":"variation","end":140428539,"alleles":["G","C","T"],"seq_region_name":"7","id":"rs1212330373","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1345124818","source":"dbSNP","start":140428540,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140428540,"alleles":["G","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs537138727","clinical_significance":[],"strand":1,"feature_type":"variation","end":140428546,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428546,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1279071227","clinical_significance":[],"start":140428549,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140428549,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140428552,"alleles":["TT","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428551,"clinical_significance":[],"seq_region_name":"7","id":"rs1228661063"},{"feature_type":"variation","strand":1,"end":140428555,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428555,"clinical_significance":[],"seq_region_name":"7","id":"rs1308938752"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1375293540","alleles":["G","T"],"end":140428559,"feature_type":"variation","strand":1,"source":"dbSNP","start":140428559,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799703764","feature_type":"variation","strand":1,"end":140428562,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428562},{"seq_region_name":"7","id":"rs1799703782","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428567,"source":"dbSNP","strand":1,"feature_type":"variation","end":140428567,"alleles":["T","C"]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428569,"feature_type":"variation","strand":1,"end":140428569,"alleles":["A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799703810"},{"seq_region_name":"7","id":"rs1799703841","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140428578,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428578,"source":"dbSNP"},{"start":140428579,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140428579,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799703869","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428583,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140428583,"clinical_significance":[],"seq_region_name":"7","id":"rs1799703887"},{"seq_region_name":"7","id":"rs1585440222","clinical_significance":[],"end":140428584,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140428584,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"feature_type":"variation","strand":1,"end":140428585,"alleles":["T","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428585,"clinical_significance":[],"id":"rs1799703918","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799703937","clinical_significance":[],"alleles":["T","C"],"end":140428588,"strand":1,"feature_type":"variation","start":140428588,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1213809993","feature_type":"variation","strand":1,"end":140428590,"alleles":["C","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428590},{"seq_region_name":"7","id":"rs1585440229","clinical_significance":[],"start":140428591,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140428591,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs555540969","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428592,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140428592},{"clinical_significance":[],"id":"rs993269676","seq_region_name":"7","source":"dbSNP","start":140428594,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140428594,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140428595,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428595,"clinical_significance":[],"seq_region_name":"7","id":"rs1799704493"},{"source":"dbSNP","start":140428596,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140428596,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs887710263"},{"start":140428600,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140428600,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799704537","clinical_significance":[]},{"start":140428601,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140428601,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1167833109","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140428602,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428602,"clinical_significance":[],"seq_region_name":"7","id":"rs370973963"},{"seq_region_name":"7","id":"rs1799704596","clinical_significance":[],"start":140428617,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140428617,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs573789862","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140428628,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428628,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1585440251","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428630,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140428630},{"seq_region_name":"7","id":"rs1585440255","clinical_significance":[],"strand":1,"feature_type":"variation","end":140428635,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428635,"source":"dbSNP"},{"end":140428637,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140428637,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1585440258","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1004770453","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428638,"feature_type":"variation","strand":1,"end":140428638,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1015607584","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428639,"feature_type":"variation","strand":1,"end":140428639,"alleles":["C","T"]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428640,"source":"dbSNP","strand":1,"feature_type":"variation","end":140428640,"alleles":["A","C","T"],"seq_region_name":"7","id":"rs1403403264","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799704767","alleles":["C","A"],"end":140428641,"feature_type":"variation","strand":1,"source":"dbSNP","start":140428641,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585440267","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428643,"feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140428643},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428644,"feature_type":"variation","strand":1,"end":140428644,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs961401670"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1416477155","source":"dbSNP","start":140428645,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140428653,"alleles":["GCCTGCTGC","GC"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140428646,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428646,"source":"dbSNP","seq_region_name":"7","id":"rs1799704834","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428648,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140428648,"seq_region_name":"7","id":"rs954484424","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799704881","clinical_significance":[],"start":140428655,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140428655,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140428664,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428664,"source":"dbSNP","seq_region_name":"7","id":"rs1585440275","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428666,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140428666,"clinical_significance":[],"id":"rs1799704945","seq_region_name":"7"},{"alleles":["C","T"],"end":140428667,"feature_type":"variation","strand":1,"source":"dbSNP","start":140428667,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1334304575"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428668,"source":"dbSNP","strand":1,"feature_type":"variation","end":140428668,"alleles":["T","C"],"seq_region_name":"7","id":"rs986395096","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130185301","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428670,"source":"dbSNP","strand":1,"feature_type":"variation","end":140428670,"alleles":["G","A"]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428672,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140428672,"clinical_significance":[],"seq_region_name":"7","id":"rs1170127931"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140428675,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428675,"source":"dbSNP","seq_region_name":"7","id":"rs1799705047","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799705071","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428676,"feature_type":"variation","strand":1,"alleles":["CC","C"],"end":140428677},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140428680,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428680,"source":"dbSNP","seq_region_name":"7","id":"rs536216615","clinical_significance":[]},{"start":140428681,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140428681,"strand":1,"feature_type":"variation","id":"rs1424770238","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","G"],"end":140428682,"feature_type":"variation","strand":1,"source":"dbSNP","start":140428682,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1420568947"},{"source":"dbSNP","start":140428685,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140428689,"alleles":["CTCTC","CTC"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799705145"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428686,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140428686,"seq_region_name":"7","id":"rs1404827203","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799705199","clinical_significance":[],"start":140428691,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140428691,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"start":140428699,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140428699,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799705218","clinical_significance":[]},{"clinical_significance":[],"id":"rs1017381298","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428700,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140428700},{"alleles":["C","T"],"end":140428702,"feature_type":"variation","strand":1,"source":"dbSNP","start":140428702,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799705272"},{"seq_region_name":"7","id":"rs1799705288","clinical_significance":[],"alleles":["T","C"],"end":140428709,"strand":1,"feature_type":"variation","start":140428709,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs977143549","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428710,"source":"dbSNP","strand":1,"feature_type":"variation","end":140428710,"alleles":["T","C"]},{"clinical_significance":[],"id":"rs1299260059","seq_region_name":"7","feature_type":"variation","strand":1,"end":140428711,"alleles":["C","A","G","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428711},{"seq_region_name":"7","id":"rs1029768136","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428712,"source":"dbSNP","strand":1,"feature_type":"variation","end":140428712,"alleles":["C","T"]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428713,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140428713,"seq_region_name":"7","id":"rs1799705409","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140428722,"alleles":["CCCTTTCCCT","CCCT"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428713,"clinical_significance":[],"seq_region_name":"7","id":"rs1799705426"},{"id":"rs1195911226","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428714,"source":"dbSNP","strand":1,"feature_type":"variation","end":140428714,"alleles":["C","G"]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428718,"feature_type":"variation","strand":1,"end":140428718,"alleles":["T","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1481386332"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585440310","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428720,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140428720},{"clinical_significance":[],"seq_region_name":"7","id":"rs1249285977","source":"dbSNP","start":140428724,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140428724,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140428725,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140428725,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs954244229","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799705552","clinical_significance":[],"start":140428726,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140428726,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1055441400","clinical_significance":[],"start":140428728,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","C"],"end":140428728,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799705604","feature_type":"variation","strand":1,"alleles":["A","-"],"end":140428728,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428728},{"id":"rs1585440320","seq_region_name":"7","clinical_significance":[],"alleles":["A","C","T"],"end":140428730,"strand":1,"feature_type":"variation","start":140428730,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428730,"source":"dbSNP","strand":1,"feature_type":"variation","end":140428730,"alleles":["A","-"],"id":"rs1799705646","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1491191552","feature_type":"variation","strand":1,"alleles":["AT","-"],"end":140428731,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428730},{"seq_region_name":"7","id":"rs1226666993","clinical_significance":[],"end":140428731,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","start":140428731,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs34310652","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428731,"feature_type":"variation","strand":1,"alleles":["TTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTT","TTTTTTTTTTTTTT","TTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTT"],"end":140428748},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799705950","feature_type":"variation","strand":1,"alleles":["T","A"],"end":140428732,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428732},{"seq_region_name":"7","id":"rs1799705975","clinical_significance":[],"start":140428733,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140428733,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140428735,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428735,"clinical_significance":[],"seq_region_name":"7","id":"rs1163281685"},{"end":140428737,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140428737,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs913905020","clinical_significance":[]},{"alleles":["T","A"],"end":140428739,"feature_type":"variation","strand":1,"source":"dbSNP","start":140428739,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799706062","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1346899460","source":"dbSNP","start":140428742,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","A","G"],"end":140428742,"feature_type":"variation","strand":1},{"id":"rs1799706120","seq_region_name":"7","clinical_significance":[],"alleles":["T","G"],"end":140428743,"strand":1,"feature_type":"variation","start":140428743,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"source":"dbSNP","start":140428746,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140428746,"alleles":["T","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1201487362"},{"feature_type":"variation","strand":1,"end":140428747,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428747,"clinical_significance":[],"seq_region_name":"7","id":"rs1247904584"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428747,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TTG","-"],"end":140428749,"seq_region_name":"7","id":"rs1420369061","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1194874062","end":140428749,"alleles":["TG","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140428748,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428749,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","-"],"end":140428749,"seq_region_name":"7","id":"rs869050044","clinical_significance":[]},{"id":"rs1460990676","seq_region_name":"7","clinical_significance":[],"end":140428749,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140428749,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1274789876","alleles":["GAG","G"],"end":140428751,"feature_type":"variation","strand":1,"source":"dbSNP","start":140428749,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"alleles":["A","G","T"],"end":140428750,"strand":1,"feature_type":"variation","start":140428750,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1209596125","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428752,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140428752,"seq_region_name":"7","id":"rs1799706286","clinical_significance":[]},{"source":"dbSNP","start":140428753,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140428753,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799706308","seq_region_name":"7"},{"alleles":["C","G","T"],"end":140428756,"feature_type":"variation","strand":1,"source":"dbSNP","start":140428756,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1264021976"},{"seq_region_name":"7","id":"rs541000163","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140428757,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428757,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428761,"source":"dbSNP","strand":1,"feature_type":"variation","end":140428761,"alleles":["C","T"],"seq_region_name":"7","id":"rs1193133708","clinical_significance":[]},{"seq_region_name":"7","id":"rs4500013","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428762,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G","T"],"end":140428762},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428765,"feature_type":"variation","strand":1,"end":140428765,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs945334448"},{"source":"dbSNP","start":140428767,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140428767,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799706533"},{"feature_type":"variation","strand":1,"end":140428769,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428769,"clinical_significance":[],"id":"rs1389949014","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799706572","clinical_significance":[],"strand":1,"feature_type":"variation","end":140428773,"alleles":["CCC","CC"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428771,"source":"dbSNP"},{"id":"rs982124446","seq_region_name":"7","clinical_significance":[],"end":140428773,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140428773,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"source":"dbSNP","start":140428775,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140428775,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1452345369"},{"seq_region_name":"7","id":"rs1585440398","clinical_significance":[],"strand":1,"feature_type":"variation","end":140428776,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428776,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140428777,"alleles":["T","A","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428777,"clinical_significance":[],"seq_region_name":"7","id":"rs1481628490"},{"end":140428779,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140428779,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1180534076"},{"strand":1,"feature_type":"variation","end":140428779,"alleles":["A","AA"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428779,"source":"dbSNP","id":"rs1799706701","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130185598","clinical_significance":[],"strand":1,"feature_type":"variation","end":140428782,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428782,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799706718","alleles":["G","A"],"end":140428784,"feature_type":"variation","strand":1,"source":"dbSNP","start":140428784,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428787,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140428787,"seq_region_name":"7","id":"rs1454424167","clinical_significance":[]},{"id":"rs928075222","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140428792,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428792,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140428793,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428793,"source":"dbSNP","id":"rs376322542","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140428794,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428794,"clinical_significance":[],"id":"rs1191462891","seq_region_name":"7"},{"id":"rs1405803860","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140428795,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428795,"source":"dbSNP"},{"id":"rs1284773590","seq_region_name":"7","clinical_significance":[],"end":140428799,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140428799,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1206809177","clinical_significance":[],"alleles":["A","G"],"end":140428800,"strand":1,"feature_type":"variation","start":140428800,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799706946","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140428803,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428803},{"seq_region_name":"7","id":"rs1799706963","clinical_significance":[],"strand":1,"feature_type":"variation","end":140428806,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428806,"source":"dbSNP"},{"end":140428809,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140428809,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1348513922","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140428811,"alleles":["A","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428811,"clinical_significance":[],"id":"rs1585440421","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1260182577","alleles":["C","G"],"end":140428812,"feature_type":"variation","strand":1,"source":"dbSNP","start":140428812,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"id":"rs1585440428","seq_region_name":"7","clinical_significance":[],"start":140428817,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140428817,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140428818,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428818,"clinical_significance":[],"seq_region_name":"7","id":"rs1235152842"},{"clinical_significance":[],"id":"rs188343152","seq_region_name":"7","source":"dbSNP","start":140428821,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140428821,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1322110453","clinical_significance":[],"start":140428823,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140428823,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1382193177","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428824,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140428824},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428825,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140428825,"seq_region_name":"7","id":"rs1799707644","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799707670","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428832,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140428832},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585440439","feature_type":"variation","strand":1,"end":140428833,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428833},{"clinical_significance":[],"seq_region_name":"7","id":"rs1381125051","alleles":["G","A"],"end":140428834,"feature_type":"variation","strand":1,"source":"dbSNP","start":140428834,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"id":"rs1799707737","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140428841,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428841,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1440546536","source":"dbSNP","start":140428842,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140428842,"feature_type":"variation","strand":1},{"end":140428843,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140428843,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799707783","clinical_significance":[]},{"source":"dbSNP","start":140428850,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140428850,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1324151302"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428851,"feature_type":"variation","strand":1,"end":140428851,"alleles":["C","G"],"clinical_significance":[],"id":"rs1799707828","seq_region_name":"7"},{"id":"rs1799707849","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428853,"source":"dbSNP","strand":1,"feature_type":"variation","end":140428853,"alleles":["C","A"]},{"feature_type":"variation","strand":1,"end":140428854,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428854,"clinical_significance":[],"seq_region_name":"7","id":"rs1799707875"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428855,"feature_type":"variation","strand":1,"end":140428855,"alleles":["T","C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1381000702"},{"alleles":["C","A","T"],"end":140428862,"feature_type":"variation","strand":1,"source":"dbSNP","start":140428862,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1332698540"},{"id":"rs112557444","seq_region_name":"7","clinical_significance":[],"end":140428864,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140428864,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140428865,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428865,"clinical_significance":[],"id":"rs1396438385","seq_region_name":"7"},{"start":140428866,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140428866,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1171358177","clinical_significance":[]},{"seq_region_name":"7","id":"rs1453479666","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428867,"source":"dbSNP","strand":1,"feature_type":"variation","end":140428867,"alleles":["A","G"]},{"start":140428868,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140428868,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1282479047","clinical_significance":[]},{"id":"rs1329590968","seq_region_name":"7","clinical_significance":[],"alleles":["T","A"],"end":140428869,"strand":1,"feature_type":"variation","start":140428869,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1445167655","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428870,"feature_type":"variation","strand":1,"end":140428870,"alleles":["A","G"]},{"end":140428871,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140428871,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1229299973"},{"id":"rs1799708100","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428873,"source":"dbSNP","strand":1,"feature_type":"variation","end":140428873,"alleles":["G","A"]},{"feature_type":"variation","strand":1,"end":140428874,"alleles":["G","A","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428874,"clinical_significance":[],"seq_region_name":"7","id":"rs1211613606"},{"clinical_significance":[],"id":"rs1262668147","seq_region_name":"7","end":140428877,"alleles":["GCGC","GC"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140428874,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"end":140428875,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140428875,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1799708317","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428876,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140428876,"clinical_significance":[],"seq_region_name":"7","id":"rs7784093"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1233831223","end":140428877,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140428877,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs575391183","clinical_significance":[],"alleles":["A","C","G"],"end":140428878,"strand":1,"feature_type":"variation","start":140428878,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"end":140428879,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140428879,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs542424667"},{"seq_region_name":"7","id":"rs1290709288","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["TG","TGTG"],"end":140428880,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428879,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428880,"source":"dbSNP","strand":1,"feature_type":"variation","end":140428880,"alleles":["G","A"],"seq_region_name":"7","id":"rs897398474","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428882,"source":"dbSNP","strand":1,"feature_type":"variation","end":140428882,"alleles":["C","A"],"seq_region_name":"7","id":"rs1799708562","clinical_significance":[]},{"source":"dbSNP","start":140428884,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140428884,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs993609777"},{"alleles":["C","T"],"end":140428887,"strand":1,"feature_type":"variation","start":140428887,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1491002899","clinical_significance":[]},{"id":"rs1197874675","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428888,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140428888},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428889,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140428889,"clinical_significance":[],"seq_region_name":"7","id":"rs1799708660"},{"seq_region_name":"7","id":"rs1417234737","clinical_significance":[],"alleles":["C","A"],"end":140428890,"strand":1,"feature_type":"variation","start":140428890,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"end":140428891,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140428891,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1429085776"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1473106449","source":"dbSNP","start":140428892,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140428892,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140428894,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140428894,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1310595739"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585440513","source":"dbSNP","start":140428895,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140428895,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1160881548","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428902,"source":"dbSNP","strand":1,"feature_type":"variation","end":140428902,"alleles":["C","T"]},{"id":"rs767761481","seq_region_name":"7","clinical_significance":[],"start":140428904,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140428904,"alleles":["G","A","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs890233267","source":"dbSNP","start":140428913,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140428913,"alleles":["A","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs147056657","source":"dbSNP","start":140428914,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","A","C"],"end":140428914,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140428919,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428919,"clinical_significance":[],"seq_region_name":"7","id":"rs1188567587"},{"seq_region_name":"7","id":"rs1585440527","clinical_significance":[],"alleles":["C","T"],"end":140428920,"strand":1,"feature_type":"variation","start":140428920,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1007283989","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428921,"feature_type":"variation","strand":1,"end":140428921,"alleles":["G","A"]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428921,"source":"dbSNP","strand":1,"feature_type":"variation","end":140428924,"alleles":["GGGG","GGGGG"],"seq_region_name":"7","id":"rs1163269461","clinical_significance":[]},{"seq_region_name":"7","id":"rs528582495","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428922,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140428922},{"id":"rs192833138","seq_region_name":"7","clinical_significance":[],"end":140428924,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140428924,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"id":"rs1403092682","seq_region_name":"7","end":140428930,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140428930,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1302450578","clinical_significance":[],"end":140428931,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140428931,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"feature_type":"variation","strand":1,"end":140428932,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428932,"clinical_significance":[],"id":"rs1241794262","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428933,"source":"dbSNP","strand":1,"feature_type":"variation","end":140428933,"alleles":["T","-"],"id":"rs1799709112","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428936,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140428936,"seq_region_name":"7","id":"rs1799709128","clinical_significance":[]},{"id":"rs1350914184","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428937,"source":"dbSNP","strand":1,"feature_type":"variation","end":140428937,"alleles":["A","G"]},{"clinical_significance":[],"id":"rs1799709171","seq_region_name":"7","end":140428939,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140428939,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140428941,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428941,"clinical_significance":[],"seq_region_name":"7","id":"rs1799709194"},{"id":"rs1563077460","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428942,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140428942},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428942,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GG","G"],"end":140428943,"seq_region_name":"7","id":"rs1194382459","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1339131507","alleles":["A","C"],"end":140428944,"feature_type":"variation","strand":1,"source":"dbSNP","start":140428944,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"alleles":["T","C"],"end":140428948,"strand":1,"feature_type":"variation","start":140428948,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1585440554","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799709297","source":"dbSNP","start":140428949,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140428949,"alleles":["C","G"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140428951,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140428951,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799709315"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428952,"feature_type":"variation","strand":1,"alleles":["G","A","C","T"],"end":140428952,"clinical_significance":[],"seq_region_name":"7","id":"rs957830441"},{"alleles":["T","A"],"end":140428954,"feature_type":"variation","strand":1,"source":"dbSNP","start":140428954,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799709359","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799709379","clinical_significance":[],"alleles":["CTCCT","CT"],"end":140428959,"strand":1,"feature_type":"variation","start":140428955,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"start":140428957,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","A"],"end":140428957,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs989362883","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140428959,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428959,"source":"dbSNP","seq_region_name":"7","id":"rs1290855456","clinical_significance":[]},{"start":140428961,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","C"],"end":140428961,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799709432","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140428963,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428963,"clinical_significance":[],"seq_region_name":"7","id":"rs1354692271"},{"seq_region_name":"7","id":"rs1446675937","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428963,"source":"dbSNP","strand":1,"feature_type":"variation","end":140428965,"alleles":["TTT","T","TT"]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428965,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140428965,"seq_region_name":"7","id":"rs1330476507","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799709529","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428966,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140428966},{"id":"rs1799709544","seq_region_name":"7","clinical_significance":[],"start":140428968,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140428968,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428969,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140428969,"seq_region_name":"7","id":"rs1799709566","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1020860769","source":"dbSNP","start":140428972,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140428972,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1399261984","clinical_significance":[],"strand":1,"feature_type":"variation","end":140428973,"alleles":["T","A","C","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428973,"source":"dbSNP"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428974,"feature_type":"variation","strand":1,"end":140428974,"alleles":["C","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1309434259"},{"seq_region_name":"7","id":"rs1799709669","clinical_significance":[],"start":140428974,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140428979,"alleles":["CCCCCC","CCCCCCC"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1415623584","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","G"],"end":140428977,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428977,"source":"dbSNP"},{"seq_region_name":"7","id":"rs966647606","clinical_significance":[],"start":140428978,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140428978,"alleles":["C","A","G","T"],"strand":1,"feature_type":"variation"},{"start":140428979,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140428979,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799709738","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799709758","clinical_significance":[],"strand":1,"feature_type":"variation","end":140428981,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428981,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1585440576","clinical_significance":[],"end":140428983,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140428983,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1234753178","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140428985,"source":"dbSNP","strand":1,"feature_type":"variation","end":140428985,"alleles":["T","C"]},{"id":"rs1179908133","seq_region_name":"7","clinical_significance":[],"start":140428987,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140428987,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1437511646","end":140428991,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140428991,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"alleles":["G","T"],"end":140428993,"feature_type":"variation","strand":1,"source":"dbSNP","start":140428993,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1274163743"},{"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140428995,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428995,"clinical_significance":[],"seq_region_name":"7","id":"rs1238595186"},{"seq_region_name":"7","id":"rs1266169984","clinical_significance":[],"end":140428996,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140428996,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"start":140428997,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140428997,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs927973817","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs138425867","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140428998,"feature_type":"variation","strand":1,"end":140428998,"alleles":["G","A"]},{"end":140428999,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140428999,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1799709973","seq_region_name":"7","clinical_significance":[]},{"start":140429000,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140429000,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","id":"rs1220953060","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799710028","alleles":["A","G"],"end":140429004,"feature_type":"variation","strand":1,"source":"dbSNP","start":140429004,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs554283445","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429005,"feature_type":"variation","strand":1,"end":140429005,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799710064","alleles":["A","G"],"end":140429006,"feature_type":"variation","strand":1,"source":"dbSNP","start":140429006,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1268750724","clinical_significance":[],"start":140429009,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140429009,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1280845159","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429010,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140429010},{"seq_region_name":"7","id":"rs1439547458","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140429011,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429011,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1375750323","clinical_significance":[],"alleles":["G","A"],"end":140429012,"strand":1,"feature_type":"variation","start":140429012,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799710172","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429014,"feature_type":"variation","strand":1,"end":140429014,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585440600","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429017,"feature_type":"variation","strand":1,"end":140429017,"alleles":["A","C"]},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140429018,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429018,"clinical_significance":[],"id":"rs1799710199","seq_region_name":"7"},{"start":140429019,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140429019,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799710222","clinical_significance":[]},{"source":"dbSNP","start":140429020,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140429020,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1326289375","seq_region_name":"7"},{"seq_region_name":"7","id":"rs768194732","clinical_significance":[],"strand":1,"feature_type":"variation","end":140429021,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429021,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1179261160","seq_region_name":"7","end":140429023,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140429023,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs532818535","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429025,"feature_type":"variation","strand":1,"end":140429025,"alleles":["C","T"]},{"id":"rs1410221266","seq_region_name":"7","clinical_significance":[],"start":140429026,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140429026,"alleles":["A","C","G"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140429027,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429027,"source":"dbSNP","id":"rs551035004","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1439272618","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429029,"feature_type":"variation","strand":1,"end":140429029,"alleles":["C","T"]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429031,"source":"dbSNP","strand":1,"feature_type":"variation","end":140429030,"alleles":["-","CCTG","CCTGCTCCACTCTTAGCATCTGGGTA"],"id":"rs1563077488","seq_region_name":"7","clinical_significance":[]},{"id":"rs1418217510","seq_region_name":"7","clinical_significance":[],"end":140429031,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140429031,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429031,"feature_type":"variation","strand":1,"end":140429043,"alleles":["TTTTTTTTTTTTT","TTTTTTTTT","TTTTTTTTTT","TTTTTTTTTTT","TTTTTTTTTTTT","TTTTTTTTTTTTTT","TTTTTTTTTTTTTTT"],"clinical_significance":[],"seq_region_name":"7","id":"rs76094018"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429035,"feature_type":"variation","strand":1,"end":140429035,"alleles":["T","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799710557"},{"alleles":["T","C"],"end":140429036,"strand":1,"feature_type":"variation","start":140429036,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs910059557","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799710600","seq_region_name":"7","alleles":["T","G"],"end":140429039,"feature_type":"variation","strand":1,"source":"dbSNP","start":140429039,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1319307415","clinical_significance":[],"start":140429043,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140429045,"alleles":["TGA","-"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1285715221","feature_type":"variation","strand":1,"end":140429044,"alleles":["G","-"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429044},{"clinical_significance":[],"seq_region_name":"7","id":"rs1386611383","end":140429044,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140429044,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140429045,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429045,"clinical_significance":[],"seq_region_name":"7","id":"rs1422185081"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1162871744","end":140429049,"alleles":["ACA","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140429047,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140429048,"alleles":["C","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429048,"clinical_significance":[],"seq_region_name":"7","id":"rs1442747456"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429050,"source":"dbSNP","strand":1,"feature_type":"variation","end":140429050,"alleles":["G","C"],"seq_region_name":"7","id":"rs1799710727","clinical_significance":[]},{"clinical_significance":[],"id":"rs2130186229","seq_region_name":"7","end":140429051,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140429051,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"id":"rs1371025074","seq_region_name":"7","clinical_significance":[],"start":140429052,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A","T"],"end":140429052,"strand":1,"feature_type":"variation"},{"start":140429053,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","G"],"end":140429053,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130186237","clinical_significance":[]},{"seq_region_name":"7","id":"rs750942497","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429056,"source":"dbSNP","strand":1,"feature_type":"variation","end":140429056,"alleles":["C","T"]},{"start":140429057,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A","C"],"end":140429057,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1296303371","clinical_significance":[]},{"end":140429063,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140429063,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799710828","seq_region_name":"7"},{"end":140429067,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140429067,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799710845","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799710868","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429069,"source":"dbSNP","strand":1,"feature_type":"variation","end":140429069,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1346922769","source":"dbSNP","start":140429071,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140429071,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1799710905","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429072,"source":"dbSNP","strand":1,"feature_type":"variation","end":140429072,"alleles":["G","T"]},{"clinical_significance":[],"id":"rs1345546494","seq_region_name":"7","end":140429075,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140429075,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429077,"feature_type":"variation","strand":1,"end":140429076,"alleles":["-","GC","GCA"],"clinical_significance":[],"seq_region_name":"7","id":"rs1372327485"},{"feature_type":"variation","strand":1,"end":140429077,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429077,"clinical_significance":[],"seq_region_name":"7","id":"rs1156945147"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1391086757","feature_type":"variation","strand":1,"alleles":["G","GG"],"end":140429078,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429078},{"seq_region_name":"7","id":"rs1419187324","clinical_significance":[],"end":140429079,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140429079,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429081,"feature_type":"variation","strand":1,"end":140429080,"alleles":["-","AGC"],"clinical_significance":[],"id":"rs1315957654","seq_region_name":"7"},{"clinical_significance":[],"id":"rs185300104","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429082,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140429082},{"seq_region_name":"7","id":"rs1395848487","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429083,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140429083},{"feature_type":"variation","strand":1,"end":140429084,"alleles":["AT","-"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429083,"clinical_significance":[],"seq_region_name":"7","id":"rs1385126563"},{"start":140429085,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","C"],"end":140429085,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs941543563","clinical_significance":[]},{"seq_region_name":"7","id":"rs536800997","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140429089,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429089,"source":"dbSNP"},{"end":140429090,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140429090,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1291709299"},{"seq_region_name":"7","id":"rs1343414976","clinical_significance":[],"end":140429093,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140429093,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"start":140429094,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140429094,"alleles":["G","A","C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1207244331","clinical_significance":[]},{"id":"rs1563077515","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429097,"source":"dbSNP","strand":1,"feature_type":"variation","end":140429097,"alleles":["G","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs548823476","source":"dbSNP","start":140429098,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140429098,"alleles":["C","G","T"],"feature_type":"variation","strand":1},{"id":"rs1799711272","seq_region_name":"7","clinical_significance":[],"end":140429101,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140429101,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140429104,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429104,"clinical_significance":[],"seq_region_name":"7","id":"rs1250041247"},{"end":140429107,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140429107,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585440687"},{"seq_region_name":"7","id":"rs575163644","clinical_significance":[],"alleles":["A","G"],"end":140429113,"strand":1,"feature_type":"variation","start":140429113,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"strand":1,"feature_type":"variation","end":140429117,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429117,"source":"dbSNP","id":"rs1563077522","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1280510093","seq_region_name":"7","alleles":["T","C"],"end":140429119,"feature_type":"variation","strand":1,"source":"dbSNP","start":140429119,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1236009992","clinical_significance":[],"start":140429120,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140429120,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140429125,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429125,"clinical_significance":[],"seq_region_name":"7","id":"rs985658984"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140429129,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429129,"clinical_significance":[],"seq_region_name":"7","id":"rs534744734"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429130,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140429130,"seq_region_name":"7","id":"rs1214961407","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140429132,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429132,"clinical_significance":[],"id":"rs1799711493","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140429134,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429134,"source":"dbSNP","seq_region_name":"7","id":"rs946971359","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429137,"source":"dbSNP","strand":1,"feature_type":"variation","end":140429137,"alleles":["C","T"],"id":"rs1287052231","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585440703","alleles":["C","G"],"end":140429141,"feature_type":"variation","strand":1,"source":"dbSNP","start":140429141,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140429143,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140429143,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs978351556","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799711598","feature_type":"variation","strand":1,"end":140429144,"alleles":["A","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429144},{"clinical_significance":[],"id":"rs552912243","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429146,"feature_type":"variation","strand":1,"end":140429146,"alleles":["T","C"]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429151,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140429151,"clinical_significance":[],"seq_region_name":"7","id":"rs934249623"},{"start":140429152,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140429152,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799711669","clinical_significance":[]},{"end":140429154,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140429154,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799711693"},{"clinical_significance":[],"id":"rs1314902574","seq_region_name":"7","source":"dbSNP","start":140429157,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140429157,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs939050526","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429164,"feature_type":"variation","strand":1,"end":140429164,"alleles":["T","A"]},{"alleles":["A","G"],"end":140429168,"feature_type":"variation","strand":1,"source":"dbSNP","start":140429168,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs189317370"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429169,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140429169,"seq_region_name":"7","id":"rs894914372","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429171,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140429171,"seq_region_name":"7","id":"rs1182365242","clinical_significance":[]},{"end":140429172,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140429172,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799711798","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs112524594","source":"dbSNP","start":140429173,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140429173,"feature_type":"variation","strand":1},{"start":140429174,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140429174,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs1048896986","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","C"],"end":140429175,"strand":1,"feature_type":"variation","start":140429175,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs887572852","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1004717909","source":"dbSNP","start":140429176,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140429176,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585440743","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429183,"feature_type":"variation","strand":1,"end":140429183,"alleles":["C","T"]},{"id":"rs1014876419","seq_region_name":"7","clinical_significance":[],"end":140429184,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140429184,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1475854929","clinical_significance":[],"end":140429187,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140429187,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"start":140429192,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140429192,"alleles":["A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1212436656","clinical_significance":[]},{"seq_region_name":"7","id":"rs1257564659","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["ATTTTGTATTTTTAGTAGAGA","ATTTTGTATTTTTAGTAGAGATTTTGTATTTTTAGTAGAGA"],"end":140429213,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429193,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429197,"source":"dbSNP","strand":1,"feature_type":"variation","end":140429197,"alleles":["T","C"],"seq_region_name":"7","id":"rs556937514","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs764393708","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429206,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140429206},{"feature_type":"variation","strand":1,"end":140429208,"alleles":["T","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429208,"clinical_significance":[],"id":"rs1430296982","seq_region_name":"7"},{"end":140429209,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140429209,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799712109"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429213,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140429213,"clinical_significance":[],"seq_region_name":"7","id":"rs901740884"},{"seq_region_name":"7","id":"rs1293246554","clinical_significance":[],"start":140429215,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140429215,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"alleles":["AG","-"],"end":140429216,"feature_type":"variation","strand":1,"source":"dbSNP","start":140429215,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1353746912","seq_region_name":"7"},{"id":"rs1217910258","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429217,"source":"dbSNP","strand":1,"feature_type":"variation","end":140429217,"alleles":["G","C","T"]},{"seq_region_name":"7","id":"rs1799712208","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429223,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140429223},{"end":140429224,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140429224,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs998212551","clinical_significance":[]},{"start":140429226,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140429226,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799712243","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1356058024","feature_type":"variation","strand":1,"end":140429227,"alleles":["T","A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429227},{"id":"rs1295161746","seq_region_name":"7","clinical_significance":[],"end":140429228,"alleles":["G","-"],"strand":1,"feature_type":"variation","start":140429228,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429228,"source":"dbSNP","strand":1,"feature_type":"variation","end":140429228,"alleles":["G","T"],"seq_region_name":"7","id":"rs1413038000","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799712303","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140429241,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429241},{"clinical_significance":[],"seq_region_name":"7","id":"rs1401695690","alleles":["C","T"],"end":140429244,"feature_type":"variation","strand":1,"source":"dbSNP","start":140429244,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140429245,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429245,"source":"dbSNP","id":"rs1298970217","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1030045444","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429246,"feature_type":"variation","strand":1,"end":140429246,"alleles":["G","A","C","T"]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429248,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140429248,"seq_region_name":"7","id":"rs1462387179","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs575182461","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140429249,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429249},{"clinical_significance":[],"seq_region_name":"7","id":"rs1420675686","end":140429253,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140429253,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"alleles":["G","A"],"end":140429254,"strand":1,"feature_type":"variation","start":140429254,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1189372012","clinical_significance":[]},{"alleles":["T","C"],"end":140429266,"feature_type":"variation","strand":1,"source":"dbSNP","start":140429266,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799712463","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1421547146","feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140429268,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429268},{"end":140429269,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140429269,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1337666194","clinical_significance":[]},{"clinical_significance":[],"id":"rs182009726","seq_region_name":"7","source":"dbSNP","start":140429272,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140429272,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1020766917","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429273,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140429273},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429275,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140429275,"clinical_significance":[],"seq_region_name":"7","id":"rs560760866"},{"feature_type":"variation","strand":1,"end":140429277,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429277,"clinical_significance":[],"seq_region_name":"7","id":"rs1022332455"},{"seq_region_name":"7","id":"rs1242619466","clinical_significance":[],"start":140429278,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140429278,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1339944924","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140429279,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429279},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799712706","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140429281,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429281},{"seq_region_name":"7","id":"rs1585440815","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140429282,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429282,"source":"dbSNP"},{"end":140429283,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140429283,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799712749","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1307874078","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429287,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140429287},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140429289,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429289,"clinical_significance":[],"seq_region_name":"7","id":"rs1393341939"},{"seq_region_name":"7","id":"rs1799712797","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429295,"source":"dbSNP","strand":1,"feature_type":"variation","end":140429295,"alleles":["G","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs150238380","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429296,"feature_type":"variation","strand":1,"end":140429296,"alleles":["G","C"]},{"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140429301,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429301,"clinical_significance":[],"id":"rs1003431818","seq_region_name":"7"},{"start":140429305,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140429305,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs978219156","clinical_significance":[]},{"start":140429306,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140429306,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799712871","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140429308,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429308,"clinical_significance":[],"seq_region_name":"7","id":"rs1442113354"},{"clinical_significance":[],"id":"rs183578670","seq_region_name":"7","alleles":["C","G","T"],"end":140429315,"feature_type":"variation","strand":1,"source":"dbSNP","start":140429315,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140429316,"alleles":["G","A","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429316,"clinical_significance":[],"seq_region_name":"7","id":"rs60796932"},{"start":140429317,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140429317,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1211186058","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140429318,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429318,"source":"dbSNP","seq_region_name":"7","id":"rs149419738","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429321,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140429321,"clinical_significance":[],"id":"rs1799713068","seq_region_name":"7"},{"seq_region_name":"7","id":"rs962770445","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140429322,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429322,"source":"dbSNP"},{"alleles":["C","A","T"],"end":140429324,"feature_type":"variation","strand":1,"source":"dbSNP","start":140429324,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799713142","seq_region_name":"7"},{"id":"rs1177716287","seq_region_name":"7","clinical_significance":[],"start":140429325,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140429325,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429327,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140429327,"clinical_significance":[],"id":"rs1799713179","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1468754548","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429329,"source":"dbSNP","strand":1,"feature_type":"variation","end":140429329,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1799713908","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429330,"source":"dbSNP","strand":1,"feature_type":"variation","end":140429343,"alleles":["GCTCCACTCTTAGC","-"]},{"seq_region_name":"7","id":"rs972926340","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140429331,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429331,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1207979165","alleles":["C","A","T"],"end":140429334,"feature_type":"variation","strand":1,"source":"dbSNP","start":140429334,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs188273592","alleles":["A","G"],"end":140429335,"feature_type":"variation","strand":1,"source":"dbSNP","start":140429335,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1261342245","alleles":["C","T"],"end":140429343,"feature_type":"variation","strand":1,"source":"dbSNP","start":140429343,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"id":"rs1202622332","seq_region_name":"7","clinical_significance":[],"alleles":["A","C","G","T"],"end":140429344,"strand":1,"feature_type":"variation","start":140429344,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429349,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140429349,"clinical_significance":[],"seq_region_name":"7","id":"rs1248159261"},{"seq_region_name":"7","id":"rs1241300078","clinical_significance":[],"start":140429350,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140429350,"alleles":["G","C","T"],"strand":1,"feature_type":"variation"},{"start":140429352,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140429352,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799714096","clinical_significance":[]},{"alleles":["G","A"],"end":140429356,"strand":1,"feature_type":"variation","start":140429356,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs947833508","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs934256868","feature_type":"variation","strand":1,"end":140429357,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429357},{"clinical_significance":[],"seq_region_name":"7","id":"rs1373628629","feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140429359,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429359},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429359,"feature_type":"variation","strand":1,"end":140429362,"alleles":["CCCC","CC"],"clinical_significance":[],"seq_region_name":"7","id":"rs1442001152"},{"feature_type":"variation","strand":1,"end":140429360,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429360,"clinical_significance":[],"id":"rs1486542734","seq_region_name":"7"},{"id":"rs1049327091","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140429364,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429364,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140429366,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429366,"source":"dbSNP","seq_region_name":"7","id":"rs1799714255","clinical_significance":[]},{"start":140429366,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140429369,"alleles":["CACA","CA"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799714276","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1184739498","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429368,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140429368},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130186729","alleles":["CC","C"],"end":140429372,"feature_type":"variation","strand":1,"source":"dbSNP","start":140429371,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"alleles":["C","A","T"],"end":140429372,"feature_type":"variation","strand":1,"source":"dbSNP","start":140429372,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1386355581"},{"seq_region_name":"7","id":"rs1288895411","clinical_significance":[],"start":140429374,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140429374,"alleles":["A","C","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799714344","source":"dbSNP","start":140429374,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["ATC","ATCATC"],"end":140429376,"feature_type":"variation","strand":1},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429377,"feature_type":"variation","strand":1,"end":140429377,"alleles":["T","C"],"clinical_significance":[],"id":"rs1799714356","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140429379,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429379,"clinical_significance":[],"seq_region_name":"7","id":"rs1799714374"},{"source":"dbSNP","start":140429380,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140429380,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799714400"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140429393,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429393,"clinical_significance":[],"seq_region_name":"7","id":"rs911557884"},{"start":140429396,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140429396,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799714455","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799714472","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140429402,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429402},{"clinical_significance":[],"id":"rs144861201","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140429404,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429404},{"alleles":["GGG","GG"],"end":140429409,"strand":1,"feature_type":"variation","start":140429407,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1157675288","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799714533","alleles":["C","T"],"end":140429410,"feature_type":"variation","strand":1,"source":"dbSNP","start":140429410,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140429410,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["CTCT","CT"],"end":140429413,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1038670395","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1396641208","clinical_significance":[],"alleles":["T","C"],"end":140429411,"strand":1,"feature_type":"variation","start":140429411,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1799714599","clinical_significance":[],"start":140429416,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140429416,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1196533203","feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140429417,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429417},{"source":"dbSNP","start":140429418,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140429418,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs893579801"},{"strand":1,"feature_type":"variation","end":140429422,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429422,"source":"dbSNP","seq_region_name":"7","id":"rs1010597268","clinical_significance":[]},{"alleles":["C","A"],"end":140429423,"feature_type":"variation","strand":1,"source":"dbSNP","start":140429423,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1206901479"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799714709","feature_type":"variation","strand":1,"end":140429426,"alleles":["G","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429426},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799714732","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429427,"feature_type":"variation","strand":1,"end":140429432,"alleles":["TCTTCT","TCT"]},{"source":"dbSNP","start":140429428,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140429428,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs940527221"},{"seq_region_name":"7","id":"rs576244937","clinical_significance":[],"start":140429433,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","G"],"end":140429433,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140429438,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429438,"source":"dbSNP","seq_region_name":"7","id":"rs1036172411","clinical_significance":[]},{"id":"rs1799714801","seq_region_name":"7","clinical_significance":[],"start":140429443,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140429443,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"alleles":["AA","-"],"end":140429444,"strand":1,"feature_type":"variation","start":140429443,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799714821","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799714838","seq_region_name":"7","feature_type":"variation","strand":1,"end":140429444,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429444},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429452,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140429452,"seq_region_name":"7","id":"rs1799714858","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799714876","source":"dbSNP","start":140429460,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140429460,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1426938230","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429464,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140429464},{"feature_type":"variation","strand":1,"end":140429465,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429465,"clinical_significance":[],"id":"rs1235271371","seq_region_name":"7"},{"start":140429472,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140429472,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585440892","clinical_significance":[]},{"start":140429480,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140429480,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1350370772","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140429481,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429481,"source":"dbSNP","seq_region_name":"7","id":"rs1273401642","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140429486,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429486,"clinical_significance":[],"seq_region_name":"7","id":"rs751517840"},{"strand":1,"feature_type":"variation","end":140429487,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429487,"source":"dbSNP","seq_region_name":"7","id":"rs997808969","clinical_significance":[]},{"seq_region_name":"7","id":"rs530433208","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429490,"source":"dbSNP","strand":1,"feature_type":"variation","end":140429490,"alleles":["C","G"]},{"seq_region_name":"7","id":"rs1799715043","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429496,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140429496},{"clinical_significance":[],"id":"rs1799715059","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429498,"feature_type":"variation","strand":1,"end":140429499,"alleles":["GG","G"]},{"start":140429499,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","T"],"end":140429499,"strand":1,"feature_type":"variation","id":"rs548784963","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","G"],"end":140429504,"feature_type":"variation","strand":1,"source":"dbSNP","start":140429504,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799715103","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1398768089","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140429505,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429505},{"clinical_significance":[],"seq_region_name":"7","id":"rs1358064557","end":140429506,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140429506,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"start":140429510,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140429510,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799715160","clinical_significance":[]},{"start":140429518,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140429518,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799715180","clinical_significance":[]},{"source":"dbSNP","start":140429520,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140429520,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799715198"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140429524,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429524,"clinical_significance":[],"seq_region_name":"7","id":"rs889822578"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1345906252","feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140429525,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429525},{"seq_region_name":"7","id":"rs1006884633","clinical_significance":[],"start":140429530,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140429530,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1434920798","clinical_significance":[],"start":140429536,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140429536,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1432931644","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429538,"source":"dbSNP","strand":1,"feature_type":"variation","end":140429538,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs959273253","source":"dbSNP","start":140429542,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140429542,"alleles":["T","A"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140429554,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429554,"source":"dbSNP","seq_region_name":"7","id":"rs1799715330","clinical_significance":[]},{"id":"rs1361788118","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["AGAAGAAGA","AGAAGA"],"end":140429564,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429556,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1799715400","seq_region_name":"7","feature_type":"variation","strand":1,"end":140429559,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429559},{"start":140429560,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140429560,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1022365206","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429562,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140429562,"clinical_significance":[],"seq_region_name":"7","id":"rs1012278058"},{"start":140429563,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140429563,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs968087865","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140429565,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429565,"source":"dbSNP","seq_region_name":"7","id":"rs567099037","clinical_significance":[]},{"seq_region_name":"7","id":"rs1016933791","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429566,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140429566},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130186929","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429571,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140429571},{"alleles":["AGGAG","AGGAGGAG"],"end":140429577,"feature_type":"variation","strand":1,"source":"dbSNP","start":140429573,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799715553"},{"feature_type":"variation","strand":1,"end":140429575,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429575,"clinical_significance":[],"seq_region_name":"7","id":"rs1799715573"},{"source":"dbSNP","start":140429576,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140429576,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs543349951"},{"id":"rs1195221671","seq_region_name":"7","clinical_significance":[],"start":140429579,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140429579,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"start":140429580,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140429580,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs534706584","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429583,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140429583,"clinical_significance":[],"seq_region_name":"7","id":"rs59232857"},{"start":140429584,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140429584,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1222564784","clinical_significance":[]},{"end":140429588,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140429588,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799715845","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799715867","clinical_significance":[],"alleles":["A","G"],"end":140429589,"strand":1,"feature_type":"variation","start":140429589,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"start":140429593,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["GC","TT"],"end":140429594,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs386718460","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1486749681","end":140429601,"alleles":["CCTCCTCC","CCTCC"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140429594,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"start":140429595,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140429595,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1276791556","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429601,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140429601,"seq_region_name":"7","id":"rs1200171360","clinical_significance":[]},{"alleles":["C","T"],"end":140429602,"feature_type":"variation","strand":1,"source":"dbSNP","start":140429602,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs571330698","seq_region_name":"7"},{"source":"dbSNP","start":140429603,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140429603,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs992783684"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429604,"feature_type":"variation","strand":1,"end":140429604,"alleles":["G","A","T"],"clinical_significance":[],"id":"rs10277843","seq_region_name":"7"},{"end":140429608,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140429608,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799716072"},{"id":"rs1799716087","seq_region_name":"7","clinical_significance":[],"alleles":["C","A","T"],"end":140429609,"strand":1,"feature_type":"variation","start":140429609,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140429611,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429611,"clinical_significance":[],"seq_region_name":"7","id":"rs911515707"},{"seq_region_name":"7","id":"rs1799716126","clinical_significance":[],"alleles":["C","T"],"end":140429612,"strand":1,"feature_type":"variation","start":140429612,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs540415557","clinical_significance":[],"strand":1,"feature_type":"variation","end":140429613,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429613,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs942936329","source":"dbSNP","start":140429615,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140429615,"alleles":["T","C"],"feature_type":"variation","strand":1},{"alleles":["C","T"],"end":140429616,"feature_type":"variation","strand":1,"source":"dbSNP","start":140429616,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs974407772"},{"id":"rs914880173","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140429625,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429625,"source":"dbSNP"},{"source":"dbSNP","start":140429629,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140429629,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs969496771"},{"id":"rs1799716262","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140429637,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429637,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1488805933","clinical_significance":[],"start":140429639,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140429639,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1331782087","clinical_significance":[],"start":140429649,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140429649,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799716324","end":140429650,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140429650,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs946486492","end":140429652,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140429652,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1042098981","clinical_significance":[],"end":140429653,"alleles":["C","A","G"],"strand":1,"feature_type":"variation","start":140429653,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"source":"dbSNP","start":140429655,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140429655,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799716363"},{"strand":1,"feature_type":"variation","end":140429658,"alleles":["TTTT","TTT"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429655,"source":"dbSNP","seq_region_name":"7","id":"rs1172605497","clinical_significance":[]},{"end":140429657,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140429657,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs902351846"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799716435","source":"dbSNP","start":140429664,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140429664,"alleles":["T","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs984435437","clinical_significance":[],"strand":1,"feature_type":"variation","end":140429666,"alleles":["T","C","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429666,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1479971788","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429667,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140429667},{"id":"rs1176023355","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429672,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140429672},{"clinical_significance":[],"seq_region_name":"7","id":"rs1476231943","end":140429674,"alleles":["TT","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140429673,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"id":"rs1585440999","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429675,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140429675},{"start":140429676,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140429676,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1408929126","clinical_significance":[]},{"source":"dbSNP","start":140429677,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140429677,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs139811230"},{"strand":1,"feature_type":"variation","end":140429679,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429679,"source":"dbSNP","seq_region_name":"7","id":"rs568774328","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["AGAG","AG"],"end":140429683,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429680,"clinical_significance":[],"id":"rs1799716808","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1438661852","clinical_significance":[],"alleles":["A","G"],"end":140429682,"strand":1,"feature_type":"variation","start":140429682,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs895093430","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429683,"source":"dbSNP","strand":1,"feature_type":"variation","end":140429683,"alleles":["G","C"]},{"source":"dbSNP","start":140429689,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140429689,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130187116"},{"source":"dbSNP","start":140429690,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140429694,"alleles":["TTCTT","TT"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1197182089"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799716904","feature_type":"variation","strand":1,"end":140429692,"alleles":["C","-"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429692},{"clinical_significance":[],"seq_region_name":"7","id":"rs1317781468","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140429693,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429693},{"source":"dbSNP","start":140429695,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140429695,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1012143633"},{"seq_region_name":"7","id":"rs940391080","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429699,"source":"dbSNP","strand":1,"feature_type":"variation","end":140429699,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs755663696","clinical_significance":[],"start":140429704,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140429704,"alleles":["G","A","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1799717015","clinical_significance":[],"strand":1,"feature_type":"variation","end":140429705,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429705,"source":"dbSNP"},{"seq_region_name":"7","id":"rs17161539","clinical_significance":[],"alleles":["T","C"],"end":140429707,"strand":1,"feature_type":"variation","start":140429707,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429712,"source":"dbSNP","strand":1,"feature_type":"variation","end":140429712,"alleles":["T","C"],"seq_region_name":"7","id":"rs1799717118","clinical_significance":[]},{"start":140429717,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","T"],"end":140429717,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799717136","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799717150","clinical_significance":[],"end":140429725,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140429725,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"id":"rs141557090","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429731,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140429731},{"clinical_significance":[],"seq_region_name":"7","id":"rs994670160","source":"dbSNP","start":140429732,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140429732,"alleles":["T","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs76904229","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140429734,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429734,"source":"dbSNP"},{"start":140429735,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","C"],"end":140429735,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799717274","clinical_significance":[]},{"source":"dbSNP","start":140429738,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140429738,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799717295"},{"id":"rs1344059679","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140429740,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429740,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140429743,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429743,"clinical_significance":[],"seq_region_name":"7","id":"rs1399372449"},{"seq_region_name":"7","id":"rs1799717355","clinical_significance":[],"start":140429753,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","C"],"end":140429753,"strand":1,"feature_type":"variation"},{"end":140429756,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140429756,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1404667181","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140429757,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429757,"source":"dbSNP","seq_region_name":"7","id":"rs540711613","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799717432","seq_region_name":"7","source":"dbSNP","start":140429762,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["AG","-"],"end":140429763,"feature_type":"variation","strand":1},{"id":"rs180997107","seq_region_name":"7","clinical_significance":[],"start":140429765,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140429765,"strand":1,"feature_type":"variation"},{"id":"rs1007327116","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429766,"source":"dbSNP","strand":1,"feature_type":"variation","end":140429766,"alleles":["C","A","T"]},{"seq_region_name":"7","id":"rs564878130","clinical_significance":[],"end":140429767,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140429767,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"start":140429769,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140429769,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799717549","clinical_significance":[]},{"seq_region_name":"7","id":"rs1234839548","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140429773,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429773,"source":"dbSNP"},{"clinical_significance":[],"id":"rs551158521","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429774,"feature_type":"variation","strand":1,"end":140429774,"alleles":["G","A","C"]},{"seq_region_name":"7","id":"rs1799717632","clinical_significance":[],"start":140429778,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140429778,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140429780,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429780,"source":"dbSNP","seq_region_name":"7","id":"rs186220515","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799717672","source":"dbSNP","start":140429790,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140429790,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1457594583","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140429791,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429791,"source":"dbSNP"},{"start":140429792,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140429792,"alleles":["G","T"],"strand":1,"feature_type":"variation","id":"rs1799717712","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs777729978","seq_region_name":"7","feature_type":"variation","strand":1,"end":140429794,"alleles":["C","A","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429794},{"seq_region_name":"7","id":"rs1254080411","clinical_significance":[],"alleles":["G","A"],"end":140429795,"strand":1,"feature_type":"variation","start":140429795,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"id":"rs1799717773","seq_region_name":"7","source":"dbSNP","start":140429797,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140429797,"feature_type":"variation","strand":1},{"alleles":["C","G","T"],"end":140429799,"strand":1,"feature_type":"variation","start":140429799,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs775662888","clinical_significance":[]},{"start":140429800,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140429800,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs1320482337","seq_region_name":"7","clinical_significance":[]},{"end":140429802,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140429802,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1287080842","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140429805,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429805,"source":"dbSNP","id":"rs1799717867","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429806,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140429806,"id":"rs1031134341","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs914911178","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429817,"feature_type":"variation","strand":1,"alleles":["CTCTC","CTC"],"end":140429821},{"start":140429821,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140429821,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs961202838","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429826,"feature_type":"variation","strand":1,"end":140429826,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1007435"},{"end":140429827,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140429827,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799718062","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799718086","alleles":["G","A"],"end":140429832,"feature_type":"variation","strand":1,"source":"dbSNP","start":140429832,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585441082","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429834,"feature_type":"variation","strand":1,"end":140429834,"alleles":["G","A"]},{"end":140429835,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140429835,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799718125"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429836,"feature_type":"variation","strand":1,"end":140429836,"alleles":["A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1024329497"},{"seq_region_name":"7","id":"rs1799718156","clinical_significance":[],"end":140429838,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140429838,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"id":"rs969642858","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140429841,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429841,"source":"dbSNP"},{"source":"dbSNP","start":140429842,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140429842,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1326390124"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799718232","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429845,"feature_type":"variation","strand":1,"end":140429845,"alleles":["G","A"]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429851,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140429851,"seq_region_name":"7","id":"rs530397808","clinical_significance":[]},{"source":"dbSNP","start":140429858,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140429858,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130187321"},{"seq_region_name":"7","id":"rs1438488717","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429859,"source":"dbSNP","strand":1,"feature_type":"variation","end":140429859,"alleles":["C","G"]},{"seq_region_name":"7","id":"rs1799718285","clinical_significance":[],"strand":1,"feature_type":"variation","end":140429866,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429866,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1015900586","clinical_significance":[],"start":140429867,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140429867,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1799718320","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429869,"feature_type":"variation","strand":1,"end":140429869,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1234387145","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429870,"feature_type":"variation","strand":1,"end":140429870,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799718374","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429876,"feature_type":"variation","strand":1,"end":140429876,"alleles":["C","T"]},{"clinical_significance":[],"id":"rs1585441095","seq_region_name":"7","end":140429881,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140429881,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140429885,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140429885,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585441097"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429889,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140429889,"clinical_significance":[],"seq_region_name":"7","id":"rs1585441101"},{"source":"dbSNP","start":140429890,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140429890,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs768722979"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429894,"feature_type":"variation","strand":1,"alleles":["C","A","G"],"end":140429894,"clinical_significance":[],"seq_region_name":"7","id":"rs1799718463"},{"clinical_significance":[],"seq_region_name":"7","id":"rs923737568","source":"dbSNP","start":140429895,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140429895,"feature_type":"variation","strand":1},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429897,"feature_type":"variation","strand":1,"end":140429897,"alleles":["G","A"],"clinical_significance":[],"id":"rs1157063897","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429900,"source":"dbSNP","strand":1,"feature_type":"variation","end":140429900,"alleles":["G","T"],"id":"rs1799718511","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130187359","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429902,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140429902},{"clinical_significance":[],"seq_region_name":"7","id":"rs1439367222","source":"dbSNP","start":140429904,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140429904,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs776960549","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429910,"feature_type":"variation","strand":1,"end":140429910,"alleles":["G","A","C"]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140429911,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429911,"clinical_significance":[],"seq_region_name":"7","id":"rs1585441110"},{"clinical_significance":[],"id":"rs1193316514","seq_region_name":"7","end":140429916,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140429916,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1407400115","source":"dbSNP","start":140429917,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140429917,"alleles":["A","C"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429920,"source":"dbSNP","strand":1,"feature_type":"variation","end":140429920,"alleles":["A","C"],"id":"rs1487762416","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799718630","source":"dbSNP","start":140429921,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140429921,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1799718654","seq_region_name":"7","alleles":["G","A"],"end":140429923,"feature_type":"variation","strand":1,"source":"dbSNP","start":140429923,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"end":140429927,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140429927,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs762172078"},{"clinical_significance":[],"id":"rs1799718710","seq_region_name":"7","end":140429928,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140429928,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs923036786","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429931,"source":"dbSNP","strand":1,"feature_type":"variation","end":140429931,"alleles":["G","T"]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140429933,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429933,"clinical_significance":[],"seq_region_name":"7","id":"rs1799718753"},{"alleles":["G","T"],"end":140429934,"strand":1,"feature_type":"variation","start":140429934,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs2130187397","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585441124","clinical_significance":[],"alleles":["T","G"],"end":140429935,"strand":1,"feature_type":"variation","start":140429935,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1220102522","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C","T"],"end":140429942,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429942,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799718810","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429945,"source":"dbSNP","strand":1,"feature_type":"variation","end":140429945,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1425334227","source":"dbSNP","start":140429956,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["CC","C"],"end":140429957,"feature_type":"variation","strand":1},{"start":140429957,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140429957,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs933177695","clinical_significance":[]},{"id":"rs576613019","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140429958,"strand":1,"feature_type":"variation","start":140429958,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs765390833","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140429967,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429967},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140429969,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140429969,"clinical_significance":[],"seq_region_name":"7","id":"rs191465808"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1056313777","source":"dbSNP","start":140429972,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140429972,"alleles":["A","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs894959150","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429974,"source":"dbSNP","strand":1,"feature_type":"variation","end":140429986,"alleles":["CAAACACACAAAC","CAAACACACAAACACACAAAC"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1337890934","source":"dbSNP","start":140429985,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140429985,"alleles":["A","C"],"feature_type":"variation","strand":1},{"start":140429986,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140429986,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","id":"rs757090870","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799719075","clinical_significance":[],"start":140429988,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","G"],"end":140429988,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1799719092","clinical_significance":[],"strand":1,"feature_type":"variation","end":140429998,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140429998,"source":"dbSNP"},{"id":"rs1439635068","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430000,"source":"dbSNP","strand":1,"feature_type":"variation","end":140430000,"alleles":["T","A","C"]},{"id":"rs985964189","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430001,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140430001},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140430006,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430006,"clinical_significance":[],"seq_region_name":"7","id":"rs1799719156"},{"clinical_significance":[],"seq_region_name":"7","id":"rs910480097","feature_type":"variation","strand":1,"end":140430019,"alleles":["C","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430019},{"id":"rs1799719185","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430021,"source":"dbSNP","strand":1,"feature_type":"variation","end":140430021,"alleles":["A","C"]},{"source":"dbSNP","start":140430022,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140430022,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799719202","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1382927181","clinical_significance":[],"start":140430024,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140430024,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1563077749","clinical_significance":[],"start":140430025,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","A"],"end":140430025,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430026,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140430026,"seq_region_name":"7","id":"rs1247477781","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799719360","clinical_significance":[],"start":140430033,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140430033,"strand":1,"feature_type":"variation"},{"end":140430034,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140430034,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1038262369","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs947277276","feature_type":"variation","strand":1,"end":140430037,"alleles":["G","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430037},{"end":140430039,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140430039,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1768247962","clinical_significance":[]},{"alleles":["C","T"],"end":140430043,"strand":1,"feature_type":"variation","start":140430043,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1799719425","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","G"],"end":140430044,"feature_type":"variation","strand":1,"source":"dbSNP","start":140430044,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1362513347"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1296463089","source":"dbSNP","start":140430048,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140430055,"alleles":["AAAGAAAG","AAAG"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140430055,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430055,"source":"dbSNP","seq_region_name":"7","id":"rs994217958","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs560661774","source":"dbSNP","start":140430060,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140430060,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130187537","source":"dbSNP","start":140430063,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140430063,"alleles":["G","T"],"feature_type":"variation","strand":1},{"end":140430064,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140430064,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1178612431","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130187544","clinical_significance":[],"start":140430072,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140430072,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"start":140430075,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140430075,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799719636","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140430079,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430079,"clinical_significance":[],"seq_region_name":"7","id":"rs1176239038"},{"id":"rs1358722253","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430086,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140430086},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430087,"feature_type":"variation","strand":1,"end":140430087,"alleles":["C","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799719694"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130187572","alleles":["A","G"],"end":140430091,"feature_type":"variation","strand":1,"source":"dbSNP","start":140430091,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140430099,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140430099,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs527848835"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799719736","source":"dbSNP","start":140430100,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140430100,"alleles":["G","A"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140430130,"alleles":["TGGGACAGCCATCGTCCTGGTGTGGGACA","TGGGACAGCCATCGTCCTGGTGTGGGACAGCCATCGTCCTGGTGTGGGACA"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430102,"source":"dbSNP","id":"rs1479117630","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430104,"feature_type":"variation","strand":1,"end":140430104,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1264669363"},{"id":"rs2130187601","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430105,"source":"dbSNP","strand":1,"feature_type":"variation","end":140430105,"alleles":["G","A"]},{"end":140430107,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140430107,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs750593756"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585441188","feature_type":"variation","strand":1,"end":140430109,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430109},{"start":140430114,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140430114,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799719840","clinical_significance":[]},{"alleles":["G","A"],"end":140430115,"feature_type":"variation","strand":1,"source":"dbSNP","start":140430115,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs903827056"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430119,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140430119,"clinical_significance":[],"seq_region_name":"7","id":"rs1799719876"},{"alleles":["G","C"],"end":140430120,"strand":1,"feature_type":"variation","start":140430120,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs780192213","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430123,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140430123,"id":"rs1018415089","seq_region_name":"7","clinical_significance":[]},{"start":140430125,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140430125,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799719927","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430127,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140430127,"clinical_significance":[],"id":"rs964139542","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140430129,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430129,"source":"dbSNP","id":"rs1799719966","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430133,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140430133,"seq_region_name":"7","id":"rs990370070","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140430134,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430134,"clinical_significance":[],"id":"rs146207905","seq_region_name":"7"},{"alleles":["C","G"],"end":140430137,"strand":1,"feature_type":"variation","start":140430137,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1052507484","clinical_significance":[]},{"seq_region_name":"7","id":"rs1563077771","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430139,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140430139},{"source":"dbSNP","start":140430140,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140430140,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1563077772"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799720072","feature_type":"variation","strand":1,"end":140430141,"alleles":["G","A","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430141},{"seq_region_name":"7","id":"rs1445328797","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["GAT","GATGAT"],"end":140430145,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430143,"source":"dbSNP"},{"alleles":["A","C"],"end":140430144,"feature_type":"variation","strand":1,"source":"dbSNP","start":140430144,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799720122"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140430145,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430145,"clinical_significance":[],"seq_region_name":"7","id":"rs116328867"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1276330581","source":"dbSNP","start":140430145,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["TT","-"],"end":140430146,"feature_type":"variation","strand":1},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430145,"feature_type":"variation","strand":1,"end":140430150,"alleles":["TTGTTT","TT"],"clinical_significance":[],"id":"rs1399492399","seq_region_name":"7"},{"id":"rs1014188194","seq_region_name":"7","clinical_significance":[],"start":140430147,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","C"],"end":140430147,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140430148,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140430148,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799720211","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140430150,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430150,"source":"dbSNP","id":"rs2130187710","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799720233","source":"dbSNP","start":140430151,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140430151,"alleles":["T","C"],"feature_type":"variation","strand":1},{"id":"rs2130187714","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140430154,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430154,"source":"dbSNP"},{"id":"rs1799720246","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430155,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140430155},{"seq_region_name":"7","id":"rs2130187724","clinical_significance":[],"end":140430157,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140430157,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430159,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140430159,"id":"rs1799720263","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799720289","clinical_significance":[],"end":140430159,"alleles":["A","-"],"strand":1,"feature_type":"variation","start":140430159,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"strand":1,"feature_type":"variation","end":140430161,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430161,"source":"dbSNP","seq_region_name":"7","id":"rs1799720304","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430163,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140430163,"seq_region_name":"7","id":"rs1799720326","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799720352","end":140430164,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140430164,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140430165,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140430165,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130187739"},{"seq_region_name":"7","id":"rs1799720365","clinical_significance":[],"start":140430168,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140430168,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"end":140430177,"alleles":["CTCCACTCCA","CTCCA"],"strand":1,"feature_type":"variation","start":140430168,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1799720379","seq_region_name":"7","clinical_significance":[]},{"end":140430170,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140430170,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799720397"},{"clinical_significance":[],"id":"rs1799720407","seq_region_name":"7","end":140430172,"alleles":["A","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140430172,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430174,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140430174,"clinical_significance":[],"id":"rs1799720424","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799720444","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430175,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140430175},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430176,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140430176,"seq_region_name":"7","id":"rs2130187760","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430180,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140430180,"clinical_significance":[],"id":"rs1799720461","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1724210712","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430181,"feature_type":"variation","strand":1,"end":140430181,"alleles":["C","T"]},{"feature_type":"variation","strand":1,"end":140430186,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430186,"clinical_significance":[],"id":"rs2130187765","seq_region_name":"7"},{"alleles":["G","C"],"end":140430191,"strand":1,"feature_type":"variation","start":140430191,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799720483","clinical_significance":[]},{"alleles":["G","A"],"end":140430192,"strand":1,"feature_type":"variation","start":140430192,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799720495","clinical_significance":[]},{"end":140430195,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140430195,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs923575303","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140430195,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140430196,"alleles":["TT","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799720541","seq_region_name":"7"},{"source":"dbSNP","start":140430200,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140430202,"alleles":["GGG","GG"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799720557","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1023774255","clinical_significance":[],"strand":1,"feature_type":"variation","end":140430201,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430201,"source":"dbSNP"},{"source":"dbSNP","start":140430206,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140430206,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799720580","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140430207,"alleles":["A","C","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430207,"source":"dbSNP","seq_region_name":"7","id":"rs1799720595","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799720633","source":"dbSNP","start":140430208,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["GATG","GATGATG"],"end":140430211,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140430213,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430213,"source":"dbSNP","seq_region_name":"7","id":"rs1171610828","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799720720","seq_region_name":"7","source":"dbSNP","start":140430214,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140430214,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799720737","feature_type":"variation","strand":1,"end":140430219,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430219},{"seq_region_name":"7","id":"rs1467611364","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430220,"source":"dbSNP","strand":1,"feature_type":"variation","end":140430220,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1444626586","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140430224,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430224},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430225,"feature_type":"variation","strand":1,"end":140430225,"alleles":["G","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs56897264"},{"id":"rs1006437323","seq_region_name":"7","clinical_significance":[],"start":140430226,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140430226,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs916427091","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430227,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140430227},{"start":140430234,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A","T"],"end":140430234,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799720895","clinical_significance":[]},{"id":"rs947905682","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140430243,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430243,"source":"dbSNP"},{"id":"rs2130187817","seq_region_name":"7","clinical_significance":[],"start":140430244,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140430244,"strand":1,"feature_type":"variation"},{"alleles":["G","T"],"end":140430246,"strand":1,"feature_type":"variation","start":140430246,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1585441239","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430249,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140430249,"id":"rs1799720956","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799720977","source":"dbSNP","start":140430250,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140430250,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140430252,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140430252,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799721000"},{"source":"dbSNP","start":140430261,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140430261,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs181469701"},{"seq_region_name":"7","id":"rs1473383710","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430267,"source":"dbSNP","strand":1,"feature_type":"variation","end":140430267,"alleles":["C","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1236636882","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430268,"feature_type":"variation","strand":1,"end":140430268,"alleles":["T","G"]},{"seq_region_name":"7","id":"rs767503503","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430270,"source":"dbSNP","strand":1,"feature_type":"variation","end":140430270,"alleles":["C","G"]},{"source":"dbSNP","start":140430273,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140430273,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799721106","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1319833529","alleles":["AAA","A"],"end":140430277,"feature_type":"variation","strand":1,"source":"dbSNP","start":140430275,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"id":"rs1799721135","seq_region_name":"7","clinical_significance":[],"alleles":["G","C"],"end":140430278,"strand":1,"feature_type":"variation","start":140430278,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs929867925","clinical_significance":[],"strand":1,"feature_type":"variation","end":140430280,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430280,"source":"dbSNP"},{"alleles":["ACCAGCTGCCTGAGCAGCTCCCCTAAAC","AC"],"end":140430308,"strand":1,"feature_type":"variation","start":140430281,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799721167","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799721180","end":140430282,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140430282,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799721203","source":"dbSNP","start":140430283,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140430283,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430288,"source":"dbSNP","strand":1,"feature_type":"variation","end":140430288,"alleles":["G","T"],"seq_region_name":"7","id":"rs1218008650","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130187867","clinical_significance":[],"end":140430290,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140430290,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1047070129","clinical_significance":[],"end":140430292,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140430292,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"id":"rs2130187872","seq_region_name":"7","end":140430300,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140430300,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799721259","source":"dbSNP","start":140430308,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140430308,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1315000119","source":"dbSNP","start":140430313,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140430313,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1394482459","source":"dbSNP","start":140430316,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140430316,"alleles":["A","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs961741033","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430317,"source":"dbSNP","strand":1,"feature_type":"variation","end":140430317,"alleles":["C","A"]},{"alleles":["C","G"],"end":140430318,"feature_type":"variation","strand":1,"source":"dbSNP","start":140430318,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799721317"},{"source":"dbSNP","start":140430321,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140430321,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1299054822","seq_region_name":"7"},{"end":140430323,"alleles":["A","AA"],"strand":1,"feature_type":"variation","start":140430323,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs560621760","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","C"],"end":140430326,"feature_type":"variation","strand":1,"source":"dbSNP","start":140430326,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799721379"},{"start":140430327,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140430327,"alleles":["G","T"],"strand":1,"feature_type":"variation","id":"rs1799721401","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1454238908","end":140430330,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140430330,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"start":140430332,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140430332,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs971710229","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140430336,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430336,"source":"dbSNP","id":"rs1030517990","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140430342,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430342,"source":"dbSNP","id":"rs1039728064","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430343,"feature_type":"variation","strand":1,"end":140430343,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs899919718"},{"alleles":["T","G"],"end":140430345,"feature_type":"variation","strand":1,"source":"dbSNP","start":140430345,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1368503413","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799721551","source":"dbSNP","start":140430349,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140430349,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1166326970","source":"dbSNP","start":140430352,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140430352,"feature_type":"variation","strand":1},{"alleles":["A","C"],"end":140430354,"feature_type":"variation","strand":1,"source":"dbSNP","start":140430354,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1312348580"},{"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140430355,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430355,"clinical_significance":[],"seq_region_name":"7","id":"rs550287789"},{"source":"dbSNP","start":140430359,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140430359,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1412636255"},{"start":140430365,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140430365,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799721649","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430370,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140430370,"clinical_significance":[],"seq_region_name":"7","id":"rs954463146"},{"id":"rs1585441285","seq_region_name":"7","clinical_significance":[],"end":140430374,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140430374,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430376,"source":"dbSNP","strand":1,"feature_type":"variation","end":140430376,"alleles":["A","C"],"id":"rs1585441287","seq_region_name":"7","clinical_significance":[]},{"start":140430377,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140430377,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","id":"rs568538931","seq_region_name":"7","clinical_significance":[]},{"id":"rs1799721757","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140430383,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430383,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140430390,"alleles":["A","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430390,"clinical_significance":[],"id":"rs113122576","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799721802","clinical_significance":[],"start":140430391,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140430391,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1236200126","seq_region_name":"7","source":"dbSNP","start":140430392,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140430394,"alleles":["TTT","TTTTT"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140430394,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140430394,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs986383663"},{"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140430395,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430395,"clinical_significance":[],"seq_region_name":"7","id":"rs1021735304"},{"end":140430398,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140430398,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799721881"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799721906","feature_type":"variation","strand":1,"end":140430403,"alleles":["AAA","AA"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430401},{"end":140430402,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140430402,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799721929","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799721945","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430407,"feature_type":"variation","strand":1,"end":140430407,"alleles":["C","G","T"]},{"seq_region_name":"7","id":"rs1474049105","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140430413,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430413,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799722001","clinical_significance":[],"end":140430425,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140430425,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1585441304","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430426,"source":"dbSNP","strand":1,"feature_type":"variation","end":140430426,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs910352449","clinical_significance":[],"start":140430432,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140430432,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"id":"rs967669300","seq_region_name":"7","clinical_significance":[],"start":140430433,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140430433,"strand":1,"feature_type":"variation"},{"end":140430439,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140430439,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs947310066"},{"id":"rs1213713631","seq_region_name":"7","clinical_significance":[],"start":140430440,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140430440,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140430444,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140430444,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1242673682"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799722112","end":140430446,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140430446,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430448,"feature_type":"variation","strand":1,"alleles":["CAGTT","-"],"end":140430452,"clinical_significance":[],"seq_region_name":"7","id":"rs1257669569"},{"end":140430449,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140430449,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799722157","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799722175","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430450,"feature_type":"variation","strand":1,"end":140430450,"alleles":["G","A"]},{"feature_type":"variation","strand":1,"end":140430454,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430454,"clinical_significance":[],"seq_region_name":"7","id":"rs978690012"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430458,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TTT","TT"],"end":140430460,"seq_region_name":"7","id":"rs1331140390","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140430461,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430461,"source":"dbSNP","seq_region_name":"7","id":"rs1799722224","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430463,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140430463,"seq_region_name":"7","id":"rs1442227582","clinical_significance":[]},{"id":"rs376721610","seq_region_name":"7","clinical_significance":[],"start":140430465,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140430465,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140430468,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140430468,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1393540208"},{"id":"rs1294714645","seq_region_name":"7","clinical_significance":[],"start":140430470,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","G","T"],"end":140430470,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430471,"source":"dbSNP","strand":1,"feature_type":"variation","end":140430471,"alleles":["G","A"],"seq_region_name":"7","id":"rs186267841","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["GGG","GG"],"end":140430473,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430471,"clinical_significance":[],"seq_region_name":"7","id":"rs1367453732"},{"seq_region_name":"7","id":"rs1799722400","clinical_significance":[],"start":140430472,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140430472,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs554482434","seq_region_name":"7","alleles":["G","A"],"end":140430473,"feature_type":"variation","strand":1,"source":"dbSNP","start":140430473,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1799722457","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430481,"source":"dbSNP","strand":1,"feature_type":"variation","end":140430481,"alleles":["A","G"]},{"source":"dbSNP","start":140430483,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140430483,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1052421369"},{"clinical_significance":[],"id":"rs1799722499","seq_region_name":"7","alleles":["T","C","G"],"end":140430484,"feature_type":"variation","strand":1,"source":"dbSNP","start":140430484,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140430485,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430485,"clinical_significance":[],"seq_region_name":"7","id":"rs532276258"},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140430488,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430488,"clinical_significance":[],"id":"rs1585441350","seq_region_name":"7"},{"seq_region_name":"7","id":"rs916376633","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140430490,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430490,"source":"dbSNP"},{"end":140430496,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140430496,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs973929560","clinical_significance":[]},{"alleles":["A","T"],"end":140430497,"strand":1,"feature_type":"variation","start":140430497,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1286910463","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799722644","clinical_significance":[],"end":140430498,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140430498,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs755966296","source":"dbSNP","start":140430500,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","C","G"],"end":140430500,"feature_type":"variation","strand":1},{"start":140430501,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","T"],"end":140430501,"strand":1,"feature_type":"variation","id":"rs777594998","seq_region_name":"7","clinical_significance":[]},{"start":140430503,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","A"],"end":140430503,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1194562801","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799722737","clinical_significance":[],"alleles":["C","A","G"],"end":140430507,"strand":1,"feature_type":"variation","start":140430507,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"strand":1,"feature_type":"variation","end":140430512,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430512,"source":"dbSNP","seq_region_name":"7","id":"rs1799722767","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140430515,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430515,"clinical_significance":[],"id":"rs1045642052","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs929927192","end":140430520,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140430520,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs774700292","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430521,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CCCC","CCCCC"],"end":140430524},{"end":140430523,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140430523,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1333266151","clinical_significance":[]},{"seq_region_name":"7","id":"rs1299814260","clinical_significance":[],"start":140430531,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140430531,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585441383","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430533,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140430533},{"clinical_significance":[],"seq_region_name":"7","id":"rs1386763383","end":140430534,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140430534,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140430538,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430538,"source":"dbSNP","seq_region_name":"7","id":"rs1799722908","clinical_significance":[]},{"end":140430541,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140430541,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1389360632","clinical_significance":[]},{"alleles":["T","C"],"end":140430548,"feature_type":"variation","strand":1,"source":"dbSNP","start":140430548,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799722949","seq_region_name":"7"},{"alleles":["C","A","T"],"end":140430549,"feature_type":"variation","strand":1,"source":"dbSNP","start":140430549,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs905398570","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs753476395","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430550,"feature_type":"variation","strand":1,"end":140430550,"alleles":["G","A","T"]},{"seq_region_name":"7","id":"rs1157769910","clinical_significance":[],"start":140430552,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140430552,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs367816036","clinical_significance":[],"strand":1,"feature_type":"variation","end":140430553,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430553,"source":"dbSNP"},{"seq_region_name":"7","id":"rs778327721","clinical_significance":[],"alleles":["G","C"],"end":140430555,"strand":1,"feature_type":"variation","start":140430555,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1799723086","clinical_significance":[],"start":140430557,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140430557,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs748570250","source":"dbSNP","start":140430559,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140430559,"alleles":["G","A"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140430563,"alleles":["G","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430563,"clinical_significance":[],"seq_region_name":"7","id":"rs1799723130"},{"clinical_significance":[],"id":"rs1799723149","seq_region_name":"7","alleles":["C","T"],"end":140430564,"feature_type":"variation","strand":1,"source":"dbSNP","start":140430564,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"id":"rs59814044","seq_region_name":"7","clinical_significance":[],"start":140430565,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A","T"],"end":140430565,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["G","GATG"],"end":140430565,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430565,"source":"dbSNP","seq_region_name":"7","id":"rs1799723234","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430567,"source":"dbSNP","strand":1,"feature_type":"variation","end":140430567,"alleles":["A","G"],"seq_region_name":"7","id":"rs1430402930","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140430568,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430568,"source":"dbSNP","id":"rs761259236","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430570,"feature_type":"variation","strand":1,"end":140430570,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799723293"},{"end":140430571,"alleles":["CC","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140430570,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1263943442"},{"seq_region_name":"7","id":"rs1585441440","clinical_significance":[],"start":140430571,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140430571,"strand":1,"feature_type":"variation"},{"alleles":["T","A"],"end":140430572,"strand":1,"feature_type":"variation","start":140430572,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1195958085","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["CCC","CCCC"],"end":140430580,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430578,"clinical_significance":[],"seq_region_name":"7","id":"rs34675966"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430580,"source":"dbSNP","strand":1,"feature_type":"variation","end":140430580,"alleles":["C","G"],"seq_region_name":"7","id":"rs1799723378","clinical_significance":[]},{"end":140430583,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140430583,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799723398"},{"seq_region_name":"7","id":"rs944070910","clinical_significance":[],"alleles":["G","A"],"end":140430590,"strand":1,"feature_type":"variation","start":140430590,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"id":"rs1799723452","seq_region_name":"7","feature_type":"variation","strand":1,"end":140430593,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430593},{"clinical_significance":[],"id":"rs1799723468","seq_region_name":"7","alleles":["G","A","T"],"end":140430594,"feature_type":"variation","strand":1,"source":"dbSNP","start":140430594,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799723490","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430597,"feature_type":"variation","strand":1,"end":140430597,"alleles":["G","A"]},{"end":140430599,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140430599,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1285582321"},{"clinical_significance":[],"id":"rs1799723521","seq_region_name":"7","source":"dbSNP","start":140430604,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140430604,"feature_type":"variation","strand":1},{"start":140430606,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","C"],"end":140430606,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs993182485","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140430608,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430608,"source":"dbSNP","seq_region_name":"7","id":"rs1029969286","clinical_significance":[]},{"source":"dbSNP","start":140430611,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140430611,"alleles":["A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799723564","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140430615,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430615,"source":"dbSNP","seq_region_name":"7","id":"rs1201309484","clinical_significance":[]},{"start":140430618,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140430618,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1563077869","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs200557162","end":140430620,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140430620,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799723635","alleles":["G","A","T"],"end":140430623,"feature_type":"variation","strand":1,"source":"dbSNP","start":140430623,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"id":"rs1039676307","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430626,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140430626},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430627,"source":"dbSNP","strand":1,"feature_type":"variation","end":140430627,"alleles":["C","G","T"],"id":"rs1254677231","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1470777898","clinical_significance":[],"alleles":["T","A"],"end":140430633,"strand":1,"feature_type":"variation","start":140430633,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs954622972","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430637,"feature_type":"variation","strand":1,"end":140430637,"alleles":["A","C"]},{"seq_region_name":"7","id":"rs1334249067","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430640,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140430640},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799723744","source":"dbSNP","start":140430640,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140430661,"alleles":["GAGCCGAGATGGTGCCACTGCA","GAGCCGAGATGGTGCCACTGCATTCCAGCGAGCCGAGATGGTGCCACTGCA"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1278225044","seq_region_name":"7","source":"dbSNP","start":140430644,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140430644,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140430645,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140430645,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1007272393"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1382248097","feature_type":"variation","strand":1,"end":140430651,"alleles":["G","A","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430651},{"start":140430653,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","T"],"end":140430653,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799723831","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1337875761","end":140430657,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140430657,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"start":140430660,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140430660,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1017770543","clinical_significance":[]},{"source":"dbSNP","start":140430661,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140430661,"alleles":["A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs968558467"},{"clinical_significance":[],"id":"rs11974068","seq_region_name":"7","source":"dbSNP","start":140430662,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140430662,"alleles":["C","T"],"feature_type":"variation","strand":1},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430669,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140430669,"clinical_significance":[],"id":"rs139592413","seq_region_name":"7"},{"id":"rs544721677","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140430670,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430670,"source":"dbSNP"},{"source":"dbSNP","start":140430671,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140430671,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799724043"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430672,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140430672,"clinical_significance":[],"id":"rs1424260675","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799724077","clinical_significance":[],"start":140430677,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","G"],"end":140430677,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs988552927","clinical_significance":[],"end":140430680,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140430680,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs556595784","feature_type":"variation","strand":1,"end":140430681,"alleles":["G","A","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430681},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430683,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140430683,"clinical_significance":[],"seq_region_name":"7","id":"rs1036390060"},{"start":140430688,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140430688,"alleles":["T","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1563077898","clinical_significance":[]},{"alleles":["C","T"],"end":140430690,"strand":1,"feature_type":"variation","start":140430690,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1325395948","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1360933175","clinical_significance":[],"strand":1,"feature_type":"variation","end":140430691,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430691,"source":"dbSNP"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430693,"feature_type":"variation","strand":1,"end":140430693,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1225625345"},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140430695,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430695,"clinical_significance":[],"seq_region_name":"7","id":"rs1799724236"},{"seq_region_name":"7","id":"rs1799724248","clinical_significance":[],"start":140430696,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["AAAAA","AAAAAA"],"end":140430700,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140430698,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140430716,"alleles":["AAATAAATAAATAAATAAA","AAATAAATAAATAAA","AAATAAATAAATAAATAAATAAA"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs762757756","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1013283324","clinical_significance":[],"end":140430704,"alleles":["AAA","A"],"strand":1,"feature_type":"variation","start":140430702,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"alleles":["AAATAAA","AA"],"end":140430708,"strand":1,"feature_type":"variation","start":140430702,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799724326","clinical_significance":[]},{"clinical_significance":[],"id":"rs1260557972","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140430704,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430704},{"clinical_significance":[],"seq_region_name":"7","id":"rs949409787","end":140430714,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140430714,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["AAACAAA","AAA"],"end":140430720,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430714,"source":"dbSNP","seq_region_name":"7","id":"rs1217410665","clinical_significance":[]},{"clinical_significance":[],"id":"rs2130188303","seq_region_name":"7","feature_type":"variation","strand":1,"end":140430717,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430717},{"seq_region_name":"7","id":"rs1344430538","clinical_significance":[],"start":140430718,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140430723,"alleles":["AAATAA","AA"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs548512627","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430721,"source":"dbSNP","strand":1,"feature_type":"variation","end":140430721,"alleles":["T","A","C"]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140430724,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430724,"clinical_significance":[],"id":"rs1341913299","seq_region_name":"7"},{"id":"rs1264489760","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140430727,"strand":1,"feature_type":"variation","start":140430727,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs2130188320","clinical_significance":[],"start":140430730,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140430730,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs2130188323","seq_region_name":"7","alleles":["C","T"],"end":140430733,"feature_type":"variation","strand":1,"source":"dbSNP","start":140430733,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140430735,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430735,"source":"dbSNP","seq_region_name":"7","id":"rs926680304","clinical_significance":[]},{"source":"dbSNP","start":140430738,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140430738,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799724514"},{"id":"rs1799724540","seq_region_name":"7","clinical_significance":[],"start":140430740,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140430740,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs17161541","source":"dbSNP","start":140430742,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140430742,"alleles":["C","G","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs552823009","feature_type":"variation","strand":1,"end":140430743,"alleles":["G","A","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430743},{"start":140430744,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140430744,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs898092657","clinical_significance":[]},{"id":"rs776275607","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140430748,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430748,"source":"dbSNP"},{"source":"dbSNP","start":140430751,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140430751,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1051870889","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1458935504","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430752,"source":"dbSNP","strand":1,"feature_type":"variation","end":140430752,"alleles":["G","A","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1166101304","alleles":["G","C"],"end":140430753,"feature_type":"variation","strand":1,"source":"dbSNP","start":140430753,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140430754,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140430754,"alleles":["C","CCCCCC"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs371618656"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799724750","end":140430754,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140430754,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"id":"rs1585441559","seq_region_name":"7","clinical_significance":[],"end":140430757,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140430757,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140430759,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430759,"clinical_significance":[],"seq_region_name":"7","id":"rs1585441561"},{"seq_region_name":"7","id":"rs951253614","clinical_significance":[],"end":140430761,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140430761,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1366951477","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430762,"feature_type":"variation","strand":1,"end":140430762,"alleles":["T","G"]},{"clinical_significance":[],"id":"rs1173839130","seq_region_name":"7","feature_type":"variation","strand":1,"end":140430763,"alleles":["C","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430763},{"source":"dbSNP","start":140430764,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140430764,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs890169093"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130188386","source":"dbSNP","start":140430767,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140430767,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1007630889","seq_region_name":"7","end":140430768,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140430768,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"id":"rs1585441574","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430770,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140430770},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140430772,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430772,"source":"dbSNP","id":"rs1799724963","seq_region_name":"7","clinical_significance":[]},{"end":140430776,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140430776,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1453859032","clinical_significance":[]},{"start":140430780,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","A","T"],"end":140430780,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs369029303","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799725030","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140430782,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430782,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430788,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140430788,"seq_region_name":"7","id":"rs1240481772","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140430790,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430790,"clinical_significance":[],"id":"rs1197282783","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430792,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140430792,"seq_region_name":"7","id":"rs1799725070","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799725090","alleles":["C","A"],"end":140430798,"feature_type":"variation","strand":1,"source":"dbSNP","start":140430798,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"id":"rs1799725102","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430799,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140430799},{"seq_region_name":"7","id":"rs968423540","clinical_significance":[],"strand":1,"feature_type":"variation","end":140430804,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430804,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799725133","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430806,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140430806},{"clinical_significance":[],"seq_region_name":"7","id":"rs1271615179","end":140430809,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140430809,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1159860657","end":140430810,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140430810,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1799725189","clinical_significance":[],"alleles":["A","G"],"end":140430812,"strand":1,"feature_type":"variation","start":140430812,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"start":140430814,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140430814,"alleles":["C","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799725206","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430823,"source":"dbSNP","strand":1,"feature_type":"variation","end":140430823,"alleles":["T","C"],"seq_region_name":"7","id":"rs1228406006","clinical_significance":[]},{"alleles":["C","T"],"end":140430824,"feature_type":"variation","strand":1,"source":"dbSNP","start":140430824,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799725252","seq_region_name":"7"},{"alleles":["C","T"],"end":140430825,"strand":1,"feature_type":"variation","start":140430825,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs912508239","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140430829,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430829,"clinical_significance":[],"seq_region_name":"7","id":"rs758960064"},{"clinical_significance":[],"id":"rs1585441594","seq_region_name":"7","alleles":["T","A"],"end":140430830,"feature_type":"variation","strand":1,"source":"dbSNP","start":140430830,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"end":140430834,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140430834,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs2130188444","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430837,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140430837,"clinical_significance":[],"id":"rs2130188446","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140430838,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430838,"clinical_significance":[],"seq_region_name":"7","id":"rs2130188449"},{"alleles":["C","A"],"end":140430841,"feature_type":"variation","strand":1,"source":"dbSNP","start":140430841,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1244864063"},{"strand":1,"feature_type":"variation","end":140430847,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430847,"source":"dbSNP","seq_region_name":"7","id":"rs1381629545","clinical_significance":[]},{"seq_region_name":"7","id":"rs1333167952","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430848,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140430848},{"seq_region_name":"7","id":"rs1444430349","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430849,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140430849},{"alleles":["G","C"],"end":140430850,"feature_type":"variation","strand":1,"source":"dbSNP","start":140430850,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1031429856"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140430854,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430854,"clinical_significance":[],"seq_region_name":"7","id":"rs1324222514"},{"alleles":["A","G"],"end":140430857,"strand":1,"feature_type":"variation","start":140430857,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799725409","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430863,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140430863,"clinical_significance":[],"id":"rs10247426","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140430864,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430864,"source":"dbSNP","seq_region_name":"7","id":"rs992796509","clinical_significance":[]},{"id":"rs1799725518","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140430866,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430866,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799725538","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430867,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140430867},{"strand":1,"feature_type":"variation","end":140430869,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430869,"source":"dbSNP","seq_region_name":"7","id":"rs917145710","clinical_significance":[]},{"end":140430872,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140430872,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799725581"},{"end":140430882,"alleles":["GGGGG","GGGG"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140430878,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799725596"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799725612","source":"dbSNP","start":140430883,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140430883,"alleles":["C","T"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430886,"source":"dbSNP","strand":1,"feature_type":"variation","end":140430886,"alleles":["G","A","C","T"],"seq_region_name":"7","id":"rs1043502272","clinical_significance":[]},{"clinical_significance":[],"id":"rs970781162","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430888,"feature_type":"variation","strand":1,"end":140430888,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs903261707","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140430897,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430897,"source":"dbSNP"},{"source":"dbSNP","start":140430898,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A","C","T"],"end":140430898,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs377144394"},{"end":140430901,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140430901,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs896083324","clinical_significance":[]},{"seq_region_name":"7","id":"rs1013144192","clinical_significance":[],"start":140430903,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140430903,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140430905,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430905,"clinical_significance":[],"id":"rs369759447","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1262613761","clinical_significance":[],"start":140430907,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140430907,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1799725903","clinical_significance":[],"alleles":["G","T"],"end":140430908,"strand":1,"feature_type":"variation","start":140430908,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430910,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140430910,"seq_region_name":"7","id":"rs904819345","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140430911,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430911,"clinical_significance":[],"seq_region_name":"7","id":"rs1799726197"},{"id":"rs1799726220","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430912,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140430912},{"seq_region_name":"7","id":"rs1237705829","clinical_significance":[],"start":140430914,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140430914,"strand":1,"feature_type":"variation"},{"end":140430915,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140430915,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1372446743","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585441650","end":140430916,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140430916,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140430917,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430917,"source":"dbSNP","id":"rs190983656","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799726360","clinical_significance":[],"alleles":["C","G","T"],"end":140430918,"strand":1,"feature_type":"variation","start":140430918,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1216555403","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430920,"source":"dbSNP","strand":1,"feature_type":"variation","end":140430920,"alleles":["A","G"]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430921,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140430921,"clinical_significance":[],"id":"rs1302680235","seq_region_name":"7"},{"end":140430932,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140430932,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1420500672","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799726454","source":"dbSNP","start":140430933,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140430933,"alleles":["G","A","C"],"feature_type":"variation","strand":1},{"end":140430934,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140430934,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1293072224","clinical_significance":[]},{"id":"rs1799726499","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140430937,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430937,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799726515","clinical_significance":[],"start":140430941,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140430941,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140430942,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430942,"clinical_significance":[],"seq_region_name":"7","id":"rs183513981"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140430946,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430946,"clinical_significance":[],"seq_region_name":"7","id":"rs550306875"},{"start":140430947,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140430947,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1426383110","clinical_significance":[]},{"seq_region_name":"7","id":"rs186703037","clinical_significance":[],"end":140430950,"alleles":["T","C","G"],"strand":1,"feature_type":"variation","start":140430950,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1799726647","clinical_significance":[],"strand":1,"feature_type":"variation","end":140430956,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430956,"source":"dbSNP"},{"clinical_significance":[],"id":"rs535285568","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["TCCCTCTCCCTCTCCCTCTCCC","TCCCTCTCCCTCTCCC","TCCCTCTCCCTCTCCCTCTCCCTCTCCC"],"end":140430981,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430960},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799726717","feature_type":"variation","strand":1,"alleles":["TCCCTCTCCCTCTCCCTCTCCCCACAGTCTCCCTCTCCCTCTC","TCCCTCTCCCTCTC"],"end":140431002,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430960},{"seq_region_name":"7","id":"rs2130188605","clinical_significance":[],"start":140430961,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140430961,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1488380667","seq_region_name":"7","source":"dbSNP","start":140430963,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140430963,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1171456978","source":"dbSNP","start":140430964,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140431002,"alleles":["TCTCCCTCTCCCTCTCCCCACAGTCTCCCTCTCCCTCTC","TCTCCCTCTCCCTCTC","TCTCCCTCTCCCTCTCCCCACAGTCTCCCTCTCCCTCTCCCCACAGTCTCCCTCTCCCTCTC"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1799726833","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430965,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140430965},{"id":"rs1267100283","seq_region_name":"7","clinical_significance":[],"start":140430970,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["TCTCCCTCTCCCCACAGTCTCCCTCTCCC","TCTCCCTCTCCC"],"end":140430998,"strand":1,"feature_type":"variation"},{"start":140430974,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140430974,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs929462856","clinical_significance":[]},{"seq_region_name":"7","id":"rs190665973","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430976,"source":"dbSNP","strand":1,"feature_type":"variation","end":140430976,"alleles":["T","C","G"]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430977,"feature_type":"variation","strand":1,"end":140430982,"alleles":["CTCCCC","CTCCCCCTCCCC"],"clinical_significance":[],"id":"rs1220849394","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563077973","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430977,"feature_type":"variation","strand":1,"end":140430982,"alleles":["CTCCCC","-"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs890690533","end":140430978,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140430978,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"id":"rs1183508558","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430978,"source":"dbSNP","strand":1,"feature_type":"variation","end":140430978,"alleles":["T","-"]},{"alleles":["C","T"],"end":140430979,"feature_type":"variation","strand":1,"source":"dbSNP","start":140430979,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799727006"},{"seq_region_name":"7","id":"rs1799727018","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430980,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["-","TT"],"end":140430979},{"alleles":["C","G","T"],"end":140430980,"strand":1,"feature_type":"variation","start":140430980,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1361603712","clinical_significance":[]},{"source":"dbSNP","start":140430981,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140430981,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs943075277","seq_region_name":"7"},{"source":"dbSNP","start":140430981,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["CCACAGTCTCCCTCTCCCTCTCTTGCCAC","CCAC"],"end":140431009,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799727094"},{"clinical_significance":[],"seq_region_name":"7","id":"rs547784482","source":"dbSNP","start":140430982,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140430982,"alleles":["C","A"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["CACA","CA"],"end":140430985,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430982,"source":"dbSNP","seq_region_name":"7","id":"rs975262305","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140430985,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430985,"clinical_significance":[],"seq_region_name":"7","id":"rs566400702"},{"alleles":["G","C"],"end":140430986,"strand":1,"feature_type":"variation","start":140430986,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1360088913","clinical_significance":[]},{"start":140430986,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["GTCTCCCTCTCCCTCTCTTGCCACGGTCTCCCTCT","GTCTCCCTCT","GTCTCCCTCTCCCTCTCTTGCCACGGTCTCCCTCTCCCTCTCTTGCCACGGTCTCCCTCT"],"end":140431020,"strand":1,"feature_type":"variation","id":"rs933799838","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799727220","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140430988,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140430988},{"alleles":["C","T"],"end":140430992,"strand":1,"feature_type":"variation","start":140430992,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1178720191","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140430992,"source":"dbSNP","strand":1,"feature_type":"variation","end":140430996,"alleles":["CTCTC","CTC"],"seq_region_name":"7","id":"rs1422523276","clinical_significance":[]},{"start":140430996,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["CCC","CC"],"end":140430998,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1413225030","clinical_significance":[]},{"source":"dbSNP","start":140430997,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140430997,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799727287"},{"clinical_significance":[],"id":"rs1799727311","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["TT","-"],"end":140431004,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431003},{"strand":1,"feature_type":"variation","end":140431004,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431004,"source":"dbSNP","seq_region_name":"7","id":"rs1799727327","clinical_significance":[]},{"end":140431005,"alleles":["G","C","T"],"strand":1,"feature_type":"variation","start":140431005,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799727354","clinical_significance":[]},{"id":"rs534129882","seq_region_name":"7","clinical_significance":[],"end":140431008,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140431008,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"source":"dbSNP","start":140431009,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140431009,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs999859989"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1031379102","source":"dbSNP","start":140431010,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140431010,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140431012,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140431012,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1264786957"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799727457","feature_type":"variation","strand":1,"end":140431014,"alleles":["T","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431014},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140431017,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431017,"source":"dbSNP","seq_region_name":"7","id":"rs1184372602","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431019,"source":"dbSNP","strand":1,"feature_type":"variation","end":140431019,"alleles":["C","G"],"seq_region_name":"7","id":"rs1799727582","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799727596","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431023,"feature_type":"variation","strand":1,"end":140431023,"alleles":["T","G"]},{"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140431026,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431026,"source":"dbSNP","seq_region_name":"7","id":"rs1485366872","clinical_significance":[]},{"seq_region_name":"7","id":"rs552065017","clinical_significance":[],"start":140431027,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A","C","T"],"end":140431027,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431030,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140431030,"seq_region_name":"7","id":"rs1799727672","clinical_significance":[]},{"seq_region_name":"7","id":"rs570673519","clinical_significance":[],"start":140431031,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140431031,"alleles":["C","G","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs866347006","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140431032,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431032,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1239442488","seq_region_name":"7","end":140431034,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140431034,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799727752","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140431038,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431038},{"seq_region_name":"7","id":"rs1799727776","clinical_significance":[],"alleles":["G","A"],"end":140431039,"strand":1,"feature_type":"variation","start":140431039,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"strand":1,"feature_type":"variation","end":140431042,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431042,"source":"dbSNP","seq_region_name":"7","id":"rs1799727798","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431043,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140431043,"seq_region_name":"7","id":"rs1799727823","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140431045,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431045,"source":"dbSNP","seq_region_name":"7","id":"rs1316356038","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799727860","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431047,"source":"dbSNP","strand":1,"feature_type":"variation","end":140431047,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1799727880","clinical_significance":[],"strand":1,"feature_type":"variation","end":140431050,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431050,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1799727898","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140431054,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431054},{"id":"rs1276441541","seq_region_name":"7","clinical_significance":[],"start":140431058,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140431058,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1799727942","clinical_significance":[],"start":140431059,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140431059,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431063,"source":"dbSNP","strand":1,"feature_type":"variation","end":140431063,"alleles":["C","A"],"seq_region_name":"7","id":"rs1585441752","clinical_significance":[]},{"end":140431064,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140431064,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799727982","clinical_significance":[]},{"alleles":["T","C"],"end":140431066,"strand":1,"feature_type":"variation","start":140431066,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs970355516","clinical_significance":[]},{"seq_region_name":"7","id":"rs1220888727","clinical_significance":[],"strand":1,"feature_type":"variation","end":140431070,"alleles":["A","C","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431070,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1799728052","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431071,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140431071},{"clinical_significance":[],"seq_region_name":"7","id":"rs980809654","source":"dbSNP","start":140431072,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140431072,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130188789","source":"dbSNP","start":140431074,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140431074,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1380206956","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431080,"feature_type":"variation","strand":1,"end":140431080,"alleles":["C","A","T"]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140431093,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431093,"source":"dbSNP","seq_region_name":"7","id":"rs1799728106","clinical_significance":[]},{"source":"dbSNP","start":140431094,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140431094,"alleles":["T","A","C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1265277302","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799728150","clinical_significance":[],"strand":1,"feature_type":"variation","end":140431097,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431097,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799728170","feature_type":"variation","strand":1,"end":140431100,"alleles":["T","C","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431100},{"end":140431101,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140431101,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1446297554","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799728221","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431103,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140431103},{"clinical_significance":[],"id":"rs1033645879","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431104,"feature_type":"variation","strand":1,"end":140431104,"alleles":["G","A","C"]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431111,"feature_type":"variation","strand":1,"end":140431111,"alleles":["T","C"],"clinical_significance":[],"id":"rs1799728270","seq_region_name":"7"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431112,"feature_type":"variation","strand":1,"end":140431112,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1197216321"},{"clinical_significance":[],"seq_region_name":"7","id":"rs537945078","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431113,"feature_type":"variation","strand":1,"end":140431113,"alleles":["C","G","T"]},{"seq_region_name":"7","id":"rs973524457","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431114,"source":"dbSNP","strand":1,"feature_type":"variation","end":140431114,"alleles":["G","A","C"]},{"seq_region_name":"7","id":"rs1799728364","clinical_significance":[],"start":140431116,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140431116,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1183299943","feature_type":"variation","strand":1,"end":140431119,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431119},{"strand":1,"feature_type":"variation","alleles":["GG","GGGG"],"end":140431122,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431121,"source":"dbSNP","seq_region_name":"7","id":"rs1459813139","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799728414","end":140431122,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140431122,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["C","A","G","T"],"end":140431123,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431123,"clinical_significance":[],"seq_region_name":"7","id":"rs556656549"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431124,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140431124,"clinical_significance":[],"seq_region_name":"7","id":"rs574991538"},{"start":140431125,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140431125,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs929521244","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140431126,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431126,"source":"dbSNP","id":"rs535823841","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140431127,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431127,"clinical_significance":[],"seq_region_name":"7","id":"rs554226142"},{"seq_region_name":"7","id":"rs572632690","clinical_significance":[],"strand":1,"feature_type":"variation","end":140431128,"alleles":["A","C","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431128,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140431129,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431129,"source":"dbSNP","id":"rs899406555","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","T"],"end":140431130,"feature_type":"variation","strand":1,"source":"dbSNP","start":140431130,"consequence_type":"TF_binding_site_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs546502150"},{"consequence_type":"TF_binding_site_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431131,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140431131,"clinical_significance":[],"seq_region_name":"7","id":"rs1300125179"},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140431132,"consequence_type":"TF_binding_site_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431132,"clinical_significance":[],"id":"rs1799728651","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1483794491","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"TF_binding_site_variant","start":140431133,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140431133},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799728681","feature_type":"variation","strand":1,"end":140431134,"alleles":["A","G"],"consequence_type":"TF_binding_site_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431134},{"clinical_significance":[],"seq_region_name":"7","id":"rs943581225","alleles":["C","A","T"],"end":140431135,"feature_type":"variation","strand":1,"source":"dbSNP","start":140431135,"consequence_type":"TF_binding_site_variant","assembly_name":"GRCh38"},{"start":140431136,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"TF_binding_site_variant","alleles":["G","A"],"end":140431136,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1038675329","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799728747","consequence_type":"TF_binding_site_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431137,"feature_type":"variation","strand":1,"end":140431137,"alleles":["C","T"]},{"end":140431141,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140431141,"consequence_type":"TF_binding_site_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799728768"},{"seq_region_name":"7","id":"rs1461036486","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"TF_binding_site_variant","start":140431142,"source":"dbSNP","strand":1,"feature_type":"variation","end":140431142,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799728805","source":"dbSNP","start":140431144,"consequence_type":"TF_binding_site_variant","assembly_name":"GRCh38","end":140431144,"alleles":["G","A"],"feature_type":"variation","strand":1},{"start":140431145,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"TF_binding_site_variant","alleles":["G","T"],"end":140431145,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1350036286","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140431146,"consequence_type":"TF_binding_site_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431146,"clinical_significance":[],"seq_region_name":"7","id":"rs1337536644"},{"alleles":["C","T"],"end":140431150,"feature_type":"variation","strand":1,"source":"dbSNP","start":140431150,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1442452343"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431151,"feature_type":"variation","strand":1,"alleles":["G","A","C","T"],"end":140431151,"clinical_significance":[],"id":"rs995618840","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140431153,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431153,"source":"dbSNP","seq_region_name":"7","id":"rs1799728896","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140431154,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431154,"source":"dbSNP","seq_region_name":"7","id":"rs1441397112","clinical_significance":[]},{"end":140431160,"alleles":["TTTTTTT","TTTTTTTT"],"strand":1,"feature_type":"variation","start":140431154,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1799728960","seq_region_name":"7","clinical_significance":[]},{"end":140431159,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140431159,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1026631919","clinical_significance":[]},{"seq_region_name":"7","id":"rs1244473559","clinical_significance":[],"alleles":["T","C","G"],"end":140431160,"strand":1,"feature_type":"variation","start":140431160,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1799729034","clinical_significance":[],"start":140431161,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["GG","G"],"end":140431162,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140431162,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140431162,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799729050"},{"seq_region_name":"7","id":"rs1267343183","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140431163,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431163,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1312584951","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431169,"source":"dbSNP","strand":1,"feature_type":"variation","end":140431169,"alleles":["C","A","G","T"]},{"end":140431170,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140431170,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs886886857"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1230002719","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431171,"feature_type":"variation","strand":1,"end":140431171,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1334421099","clinical_significance":[],"start":140431173,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140431176,"alleles":["GTTT","GTTTGTTT"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140431177,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431177,"source":"dbSNP","seq_region_name":"7","id":"rs1306915141","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140431178,"alleles":["G","A","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431178,"clinical_significance":[],"seq_region_name":"7","id":"rs1249270190"},{"seq_region_name":"7","id":"rs1457097130","clinical_significance":[],"start":140431179,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140431179,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1367671631","seq_region_name":"7","feature_type":"variation","strand":1,"end":140431180,"alleles":["T","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431180},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431185,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140431185,"seq_region_name":"7","id":"rs1003943185","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1244482873","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431186,"feature_type":"variation","strand":1,"end":140431186,"alleles":["G","T"]},{"alleles":["G","C"],"end":140431187,"strand":1,"feature_type":"variation","start":140431187,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799729344","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140431188,"alleles":["C","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431188,"clinical_significance":[],"id":"rs1019869734","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs4526278","source":"dbSNP","start":140431189,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140431189,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140431190,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140431190,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1158965505"},{"seq_region_name":"7","id":"rs1799729444","clinical_significance":[],"start":140431193,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140431199,"alleles":["CTGGTCT","CTGGTCTGGTCT"],"strand":1,"feature_type":"variation"},{"start":140431194,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140431194,"strand":1,"feature_type":"variation","id":"rs1421274740","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","C","T"],"end":140431195,"strand":1,"feature_type":"variation","start":140431195,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1361915088","clinical_significance":[]},{"source":"dbSNP","start":140431199,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140431199,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs965151583"},{"seq_region_name":"7","id":"rs1799729576","clinical_significance":[],"end":140431205,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140431205,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1433749333","clinical_significance":[],"start":140431206,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","A","T"],"end":140431206,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799729619","source":"dbSNP","start":140431209,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140431209,"feature_type":"variation","strand":1},{"alleles":["C","A"],"end":140431211,"strand":1,"feature_type":"variation","start":140431211,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1585441873","clinical_significance":[]},{"id":"rs1420068567","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140431212,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431212,"source":"dbSNP"},{"alleles":["G","A","T"],"end":140431213,"strand":1,"feature_type":"variation","start":140431213,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs576616729","clinical_significance":[]},{"id":"rs1430085691","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431214,"source":"dbSNP","strand":1,"feature_type":"variation","end":140431214,"alleles":["C","G","T"]},{"start":140431215,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140431215,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs1168137783","seq_region_name":"7","clinical_significance":[]},{"start":140431216,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140431216,"alleles":["A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs370243688","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585441882","feature_type":"variation","strand":1,"end":140431218,"alleles":["T","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431218},{"seq_region_name":"7","id":"rs996629036","clinical_significance":[],"end":140431221,"alleles":["T","C","G"],"strand":1,"feature_type":"variation","start":140431221,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1799729773","clinical_significance":[],"end":140431222,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140431222,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1422637414","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431223,"source":"dbSNP","strand":1,"feature_type":"variation","end":140431223,"alleles":["C","A","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs372449932","source":"dbSNP","start":140431224,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140431224,"feature_type":"variation","strand":1},{"id":"rs1799729843","seq_region_name":"7","clinical_significance":[],"alleles":["C","A"],"end":140431225,"strand":1,"feature_type":"variation","start":140431225,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140431226,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431226,"clinical_significance":[],"seq_region_name":"7","id":"rs2130189023"},{"feature_type":"variation","strand":1,"end":140431227,"alleles":["A","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431227,"clinical_significance":[],"seq_region_name":"7","id":"rs1799729859"},{"clinical_significance":[],"id":"rs1799729871","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431227,"feature_type":"variation","strand":1,"end":140431231,"alleles":["AGCCT","AGCCTAGCCT"]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431228,"feature_type":"variation","strand":1,"end":140431228,"alleles":["G","T"],"clinical_significance":[],"id":"rs1799729886","seq_region_name":"7"},{"seq_region_name":"7","id":"rs2130189032","clinical_significance":[],"start":140431230,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140431230,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"start":140431231,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","A","G"],"end":140431231,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799729902","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140431232,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431232,"source":"dbSNP","id":"rs1177379748","seq_region_name":"7","clinical_significance":[]},{"id":"rs1408430433","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140431233,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431233,"source":"dbSNP"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431235,"feature_type":"variation","strand":1,"end":140431235,"alleles":["C","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1445851894"},{"start":140431240,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140431240,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1302792680","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140431241,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431241,"clinical_significance":[],"seq_region_name":"7","id":"rs1585441897"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799730007","source":"dbSNP","start":140431242,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140431242,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1799730027","clinical_significance":[],"end":140431243,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140431243,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1298427932","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431244,"source":"dbSNP","strand":1,"feature_type":"variation","end":140431244,"alleles":["G","C","T"]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140431245,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431245,"clinical_significance":[],"id":"rs1382481494","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1799730104","seq_region_name":"7","alleles":["G","C"],"end":140431246,"feature_type":"variation","strand":1,"source":"dbSNP","start":140431246,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1028238123","seq_region_name":"7","end":140431248,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140431248,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585441909","source":"dbSNP","start":140431249,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140431249,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431252,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140431252,"seq_region_name":"7","id":"rs968589822","clinical_significance":[]},{"start":140431254,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A","T"],"end":140431254,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1384418754","clinical_significance":[]},{"end":140431256,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140431256,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1276769757"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431259,"feature_type":"variation","strand":1,"end":140431259,"alleles":["A","G"],"clinical_significance":[],"id":"rs1317662564","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1223778055","seq_region_name":"7","alleles":["C","T"],"end":140431260,"feature_type":"variation","strand":1,"source":"dbSNP","start":140431260,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1264559162","clinical_significance":[],"start":140431261,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140431261,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140431264,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140431264,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs543617406"},{"seq_region_name":"7","id":"rs1445521555","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431265,"source":"dbSNP","strand":1,"feature_type":"variation","end":140431265,"alleles":["T","A"]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431266,"source":"dbSNP","strand":1,"feature_type":"variation","end":140431266,"alleles":["T","C"],"seq_region_name":"7","id":"rs201246251","clinical_significance":[]},{"end":140431267,"alleles":["TG","CT"],"strand":1,"feature_type":"variation","start":140431266,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1563078054","clinical_significance":[]},{"seq_region_name":"7","id":"rs529761118","clinical_significance":[],"alleles":["G","T"],"end":140431267,"strand":1,"feature_type":"variation","start":140431267,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1242187797","clinical_significance":[],"start":140431268,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140431268,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431269,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140431269,"clinical_significance":[],"seq_region_name":"7","id":"rs1484491970"},{"id":"rs1261802984","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431272,"source":"dbSNP","strand":1,"feature_type":"variation","end":140431272,"alleles":["C","T"]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431274,"source":"dbSNP","strand":1,"feature_type":"variation","end":140431274,"alleles":["C","T"],"seq_region_name":"7","id":"rs1799730500","clinical_significance":[]},{"id":"rs2130189129","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431275,"source":"dbSNP","strand":1,"feature_type":"variation","end":140431275,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799730518","source":"dbSNP","start":140431278,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140431278,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1223512885","seq_region_name":"7","alleles":["A","G"],"end":140431285,"feature_type":"variation","strand":1,"source":"dbSNP","start":140431285,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"end":140431286,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140431286,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799730551"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431287,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140431287,"id":"rs1799730567","seq_region_name":"7","clinical_significance":[]},{"id":"rs1486839935","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140431288,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431288,"source":"dbSNP"},{"alleles":["C","G","T"],"end":140431291,"strand":1,"feature_type":"variation","start":140431291,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1278330230","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140431294,"alleles":["A","C","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431294,"clinical_significance":[],"seq_region_name":"7","id":"rs1184684043"},{"start":140431297,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140431297,"alleles":["C","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799730658","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799730688","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431298,"feature_type":"variation","strand":1,"end":140431298,"alleles":["T","A"]},{"id":"rs1229095505","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431303,"source":"dbSNP","strand":1,"feature_type":"variation","end":140431303,"alleles":["T","A","G"]},{"feature_type":"variation","strand":1,"end":140431304,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431304,"clinical_significance":[],"seq_region_name":"7","id":"rs1317289110"},{"end":140431305,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140431305,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799730743","clinical_significance":[]},{"seq_region_name":"7","id":"rs1396401322","clinical_significance":[],"start":140431306,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","C","G"],"end":140431306,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140431308,"alleles":["T","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431308,"clinical_significance":[],"seq_region_name":"7","id":"rs979202408"},{"clinical_significance":[],"id":"rs1334573546","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140431309,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431309},{"id":"rs1469275498","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140431311,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431311,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1585441936","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140431312,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431312,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1262256390","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140431317,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431317,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1172951631","clinical_significance":[],"end":140431319,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140431319,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"id":"rs924603563","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431320,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140431320},{"alleles":["C","A","G","T"],"end":140431324,"strand":1,"feature_type":"variation","start":140431324,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs113058332","clinical_significance":[]},{"seq_region_name":"7","id":"rs1177450454","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431325,"source":"dbSNP","strand":1,"feature_type":"variation","end":140431325,"alleles":["G","A","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799730998","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431326,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140431326},{"clinical_significance":[],"id":"rs1799731024","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431330,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140431330},{"seq_region_name":"7","id":"rs1258094924","clinical_significance":[],"end":140431331,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","start":140431331,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1197038172","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431333,"source":"dbSNP","strand":1,"feature_type":"variation","end":140431333,"alleles":["C","A","T"]},{"id":"rs1799731080","seq_region_name":"7","clinical_significance":[],"end":140431336,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140431336,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585441951","source":"dbSNP","start":140431337,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140431337,"alleles":["A","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1799731114","seq_region_name":"7","feature_type":"variation","strand":1,"end":140431344,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431344},{"end":140431347,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140431347,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1431649461","clinical_significance":[]},{"id":"rs1412842775","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140431350,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431350,"source":"dbSNP"},{"alleles":["C","T"],"end":140431353,"strand":1,"feature_type":"variation","start":140431353,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1585441958","clinical_significance":[]},{"source":"dbSNP","start":140431355,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C","G"],"end":140431355,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs956335078"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1384702959","source":"dbSNP","start":140431359,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140431359,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140431361,"alleles":["T","-"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431361,"clinical_significance":[],"seq_region_name":"7","id":"rs1312676913"},{"strand":1,"feature_type":"variation","end":140431361,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431361,"source":"dbSNP","id":"rs1345851627","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431362,"source":"dbSNP","strand":1,"feature_type":"variation","end":140431362,"alleles":["C","T"],"id":"rs992885895","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","T"],"end":140431363,"feature_type":"variation","strand":1,"source":"dbSNP","start":140431363,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1330913217","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1455854592","source":"dbSNP","start":140431365,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["AAA","AA"],"end":140431367,"feature_type":"variation","strand":1},{"start":140431371,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140431372,"alleles":["CC","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1395948581","clinical_significance":[]},{"id":"rs560122363","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431372,"source":"dbSNP","strand":1,"feature_type":"variation","end":140431372,"alleles":["C","G","T"]},{"alleles":["G","A","C","T"],"end":140431373,"strand":1,"feature_type":"variation","start":140431373,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1799731375","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1340333727","clinical_significance":[],"start":140431378,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140431378,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs917429029","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431384,"feature_type":"variation","strand":1,"end":140431384,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799731480","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431385,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140431385},{"seq_region_name":"7","id":"rs1585441977","clinical_significance":[],"strand":1,"feature_type":"variation","end":140431387,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431387,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1799731513","seq_region_name":"7","end":140431389,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140431389,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"start":140431391,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","G","T"],"end":140431391,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1440775201","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431392,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140431392,"clinical_significance":[],"id":"rs948899162","seq_region_name":"7"},{"source":"dbSNP","start":140431392,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["GGCCGCCACCCCGTCTGGGAAGTGAGGAGCGTCTCTGCCTGGCCGCC","GGCCGCC"],"end":140431438,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1240585108"},{"source":"dbSNP","start":140431395,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140431395,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1044579565"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1365123495","source":"dbSNP","start":140431396,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140431396,"alleles":["G","A","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1210017124","clinical_significance":[],"alleles":["A","-"],"end":140431399,"strand":1,"feature_type":"variation","start":140431399,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"id":"rs1218275501","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431400,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140431400},{"clinical_significance":[],"id":"rs1563078085","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["CCCC","CCCCC"],"end":140431403,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431400},{"seq_region_name":"7","id":"rs1289246678","clinical_significance":[],"strand":1,"feature_type":"variation","end":140431401,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431401,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1244993479","seq_region_name":"7","source":"dbSNP","start":140431402,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140431402,"feature_type":"variation","strand":1},{"start":140431403,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140431403,"alleles":["C","A","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1377443039","clinical_significance":[]},{"id":"rs1799731739","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431403,"source":"dbSNP","strand":1,"feature_type":"variation","end":140431450,"alleles":["CGTCTGGGAAGTGAGGAGCGTCTCTGCCTGGCCGCCCATCGTCTGGGA","CGTCTGGGA"]},{"seq_region_name":"7","id":"rs1284392526","clinical_significance":[],"start":140431404,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A","T"],"end":140431404,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140431406,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431406,"source":"dbSNP","seq_region_name":"7","id":"rs1799731778","clinical_significance":[]},{"start":140431407,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140431407,"alleles":["T","A","C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1335223691","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs920870100","source":"dbSNP","start":140431408,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140431408,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1426740748","clinical_significance":[],"start":140431412,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","T"],"end":140431412,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1214388735","clinical_significance":[],"end":140431418,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140431418,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1285171459","feature_type":"variation","strand":1,"end":140431421,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431421},{"seq_region_name":"7","id":"rs1490453223","clinical_significance":[],"start":140431422,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140431422,"alleles":["G","A","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1410699120","source":"dbSNP","start":140431424,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140431424,"alleles":["C","T"],"feature_type":"variation","strand":1},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431428,"feature_type":"variation","strand":1,"end":140431428,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585442023"},{"start":140431429,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140431429,"strand":1,"feature_type":"variation","id":"rs1799731975","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","C"],"end":140431431,"strand":1,"feature_type":"variation","start":140431431,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1157320296","clinical_significance":[]},{"seq_region_name":"7","id":"rs1477199276","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140431435,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431435,"source":"dbSNP"},{"clinical_significance":[],"id":"rs930897009","seq_region_name":"7","feature_type":"variation","strand":1,"end":140431436,"alleles":["G","A","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431436},{"seq_region_name":"7","id":"rs1799732083","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431441,"source":"dbSNP","strand":1,"feature_type":"variation","end":140431441,"alleles":["T","C"]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431442,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140431442,"seq_region_name":"7","id":"rs1048554496","clinical_significance":[]},{"end":140431443,"alleles":["G","A","C","T"],"strand":1,"feature_type":"variation","start":140431443,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1408863528","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799732148","clinical_significance":[],"start":140431444,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140431444,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140431449,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431449,"source":"dbSNP","seq_region_name":"7","id":"rs1799732172","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1420921439","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431452,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140431452},{"seq_region_name":"7","id":"rs1349907032","clinical_significance":[],"start":140431455,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140431455,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585442043","alleles":["C","A","T"],"end":140431460,"feature_type":"variation","strand":1,"source":"dbSNP","start":140431460,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140431461,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140431461,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799732242"},{"seq_region_name":"7","id":"rs1157393194","clinical_significance":[],"strand":1,"feature_type":"variation","end":140431462,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431462,"source":"dbSNP"},{"id":"rs370333424","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140431465,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431465,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431468,"source":"dbSNP","strand":1,"feature_type":"variation","end":140431468,"alleles":["C","A","T"],"seq_region_name":"7","id":"rs866044618","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1305412795","source":"dbSNP","start":140431469,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140431469,"feature_type":"variation","strand":1},{"start":140431470,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140431470,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs1348470004","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1347271832","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431471,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140431471},{"seq_region_name":"7","id":"rs1435374023","clinical_significance":[],"alleles":["G","A"],"end":140431472,"strand":1,"feature_type":"variation","start":140431472,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1157421459","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140431474,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431474,"source":"dbSNP"},{"alleles":["C","A","T"],"end":140431476,"feature_type":"variation","strand":1,"source":"dbSNP","start":140431476,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1279720117","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1426505280","seq_region_name":"7","alleles":["A","C"],"end":140431479,"feature_type":"variation","strand":1,"source":"dbSNP","start":140431479,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799732482","source":"dbSNP","start":140431480,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140431479,"alleles":["-","TC"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140431480,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431480,"clinical_significance":[],"seq_region_name":"7","id":"rs1799732496"},{"seq_region_name":"7","id":"rs2130189423","clinical_significance":[],"end":140431485,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140431485,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140431486,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431486,"source":"dbSNP","seq_region_name":"7","id":"rs1374921173","clinical_significance":[]},{"alleles":["AAGTGAGGAGCGTCTCTGCCCGGCC","AAGTGAGGAGCGTCTCTGCCCGGCCACCATCCCATCTAGGAAGTGAGGAGCGTCTCTGCCCGGCC"],"end":140431511,"feature_type":"variation","strand":1,"source":"dbSNP","start":140431487,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799732532","seq_region_name":"7"},{"id":"rs1204063206","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140431554,"alleles":["AAGTGAGGAGCGTCTCTGCCCGGCCGCCATCCCATCTAGGAAGTGAGGAGCGTCTCTGCCCGGCCGCC","AAGTGAGGAGCGTCTCTGCCCGGCCGCC"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431487,"source":"dbSNP"},{"source":"dbSNP","start":140431488,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140431488,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799732572","seq_region_name":"7"},{"id":"rs199723727","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431489,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140431489},{"end":140431490,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140431490,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1426645447","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431492,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140431492,"id":"rs1198213708","seq_region_name":"7","clinical_significance":[]},{"id":"rs1486002614","seq_region_name":"7","clinical_significance":[],"end":140431494,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140431494,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"end":140431497,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140431497,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1243590502"},{"feature_type":"variation","strand":1,"end":140431498,"alleles":["G","A","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431498,"clinical_significance":[],"seq_region_name":"7","id":"rs1308461896"},{"feature_type":"variation","strand":1,"end":140431499,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431499,"clinical_significance":[],"id":"rs1446295089","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799732739","clinical_significance":[],"start":140431502,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140431502,"strand":1,"feature_type":"variation"},{"start":140431504,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140431504,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1279223164","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799732774","clinical_significance":[],"alleles":["C","G"],"end":140431506,"strand":1,"feature_type":"variation","start":140431506,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"id":"rs1360142940","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431507,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140431507},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431508,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140431508,"clinical_significance":[],"seq_region_name":"7","id":"rs1224618379"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1287512397","alleles":["C","T"],"end":140431511,"feature_type":"variation","strand":1,"source":"dbSNP","start":140431511,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1450794810","clinical_significance":[],"alleles":["G","A"],"end":140431512,"strand":1,"feature_type":"variation","start":140431512,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1287430050","clinical_significance":[],"start":140431514,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140431517,"alleles":["CATC","C"],"strand":1,"feature_type":"variation"},{"end":140431516,"alleles":["T","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140431516,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1430446656"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799732929","feature_type":"variation","strand":1,"alleles":["CCCATCTAGGAAGTGAGGAGCGTCTCTGCCCGGCCGCCCATCATCTGAGATGTGGGGAGCACCTCTGCCCTGCCGCCCCATCT","CCCATCT"],"end":140431599,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431517},{"clinical_significance":[],"seq_region_name":"7","id":"rs1221157121","alleles":["C","A"],"end":140431518,"feature_type":"variation","strand":1,"source":"dbSNP","start":140431518,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140431520,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431520,"clinical_significance":[],"seq_region_name":"7","id":"rs1339233463"},{"seq_region_name":"7","id":"rs1799732976","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140431522,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431522,"source":"dbSNP"},{"start":140431524,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140431524,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1233604492","clinical_significance":[]},{"source":"dbSNP","start":140431528,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140431528,"alleles":["A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1471209383"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140431529,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431529,"source":"dbSNP","seq_region_name":"7","id":"rs1175123654","clinical_significance":[]},{"alleles":["T","C","G"],"end":140431530,"feature_type":"variation","strand":1,"source":"dbSNP","start":140431530,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1428673699","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799733066","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431531,"feature_type":"variation","strand":1,"end":140431531,"alleles":["G","A"]},{"start":140431532,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140431532,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1421222389","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140431534,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431534,"clinical_significance":[],"seq_region_name":"7","id":"rs2130189503"},{"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140431537,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431537,"clinical_significance":[],"seq_region_name":"7","id":"rs886738668"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1243567744","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431538,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140431538},{"clinical_significance":[],"seq_region_name":"7","id":"rs1379763818","source":"dbSNP","start":140431539,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140431539,"alleles":["T","C"],"feature_type":"variation","strand":1},{"start":140431540,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140431586,"alleles":["CTCTGCCCGGCCGCCCATCATCTGAGATGTGGGGAGCACCTCTGCCC","CTCTGCCC"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799733171","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140431543,"alleles":["T","TT"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431543,"source":"dbSNP","seq_region_name":"7","id":"rs1799733196","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799733222","feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140431544,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431544},{"seq_region_name":"7","id":"rs1799733247","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431546,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140431546},{"clinical_significance":[],"seq_region_name":"7","id":"rs1445810659","feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140431547,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431547},{"clinical_significance":[],"seq_region_name":"7","id":"rs1165996316","feature_type":"variation","strand":1,"alleles":["G","A","C","T"],"end":140431548,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431548},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799733335","source":"dbSNP","start":140431548,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140431549,"alleles":["GG","G"],"feature_type":"variation","strand":1},{"end":140431550,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140431550,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799733353"},{"seq_region_name":"7","id":"rs1412106394","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431551,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","G","T"],"end":140431551},{"clinical_significance":[],"id":"rs1405095699","seq_region_name":"7","alleles":["G","A"],"end":140431552,"feature_type":"variation","strand":1,"source":"dbSNP","start":140431552,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1799733429","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431553,"source":"dbSNP","strand":1,"feature_type":"variation","end":140431555,"alleles":["CCC","CC"]},{"alleles":["C","T"],"end":140431554,"strand":1,"feature_type":"variation","start":140431554,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799733445","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431556,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140431556,"clinical_significance":[],"seq_region_name":"7","id":"rs2130189575"},{"feature_type":"variation","strand":1,"end":140431558,"alleles":["C","CCC"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431558,"clinical_significance":[],"id":"rs1799733464","seq_region_name":"7"},{"id":"rs1317639858","seq_region_name":"7","clinical_significance":[],"end":140431559,"alleles":["A","G","T"],"strand":1,"feature_type":"variation","start":140431559,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1799733510","clinical_significance":[],"start":140431563,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140431563,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140431564,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431564,"source":"dbSNP","id":"rs1329128512","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140431566,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140431566,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1355861421"},{"source":"dbSNP","start":140431567,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140431567,"alleles":["T","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1451045072","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140431568,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431568,"clinical_significance":[],"seq_region_name":"7","id":"rs1382699276"},{"source":"dbSNP","start":140431571,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140431571,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799733607"},{"source":"dbSNP","start":140431572,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140431613,"alleles":["GGAGCACCTCTGCCCTGCCGCCCCATCTGGGATGTGAGGAGC","GGAGC"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1444105494"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1335420805","feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140431576,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431576},{"clinical_significance":[],"seq_region_name":"7","id":"rs200891476","alleles":["A","C","G","T"],"end":140431577,"feature_type":"variation","strand":1,"source":"dbSNP","start":140431577,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"end":140431579,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140431579,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1382843098"},{"start":140431582,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","G"],"end":140431582,"strand":1,"feature_type":"variation","id":"rs2130189620","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1409057360","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140431584,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431584,"source":"dbSNP"},{"start":140431585,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140431585,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799733759","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140431587,"alleles":["T","A","C","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431587,"clinical_significance":[],"id":"rs1248140520","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1799733804","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431588,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140431588},{"strand":1,"feature_type":"variation","end":140431589,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431589,"source":"dbSNP","seq_region_name":"7","id":"rs1185207489","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1282304045","end":140431590,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140431590,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140431591,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431591,"source":"dbSNP","seq_region_name":"7","id":"rs1355388742","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1177778694","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431594,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140431594},{"seq_region_name":"7","id":"rs1799733892","clinical_significance":[],"strand":1,"feature_type":"variation","end":140431594,"alleles":["-","AT"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431595,"source":"dbSNP"},{"start":140431595,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140431595,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799733905","clinical_significance":[]},{"alleles":["A","C","G","T"],"end":140431596,"strand":1,"feature_type":"variation","start":140431596,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs201708099","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799733966","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431597,"source":"dbSNP","strand":1,"feature_type":"variation","end":140431597,"alleles":["T","A","C"]},{"seq_region_name":"7","id":"rs1799733988","clinical_significance":[],"start":140431597,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["TCTGGGATGTGAGGAGCGTCTCTGCCTGGCCGCCCCGTCTG","TCTG"],"end":140431637,"strand":1,"feature_type":"variation"},{"alleles":["T","C"],"end":140431599,"feature_type":"variation","strand":1,"source":"dbSNP","start":140431599,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1274845304"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799734020","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431601,"feature_type":"variation","strand":1,"end":140431601,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130189666","source":"dbSNP","start":140431602,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140431602,"feature_type":"variation","strand":1},{"alleles":["T","A","C","G"],"end":140431604,"strand":1,"feature_type":"variation","start":140431604,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1585442165","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140431605,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431605,"clinical_significance":[],"seq_region_name":"7","id":"rs1294313933"},{"clinical_significance":[],"id":"rs1244253500","seq_region_name":"7","alleles":["T","A"],"end":140431606,"feature_type":"variation","strand":1,"source":"dbSNP","start":140431606,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"id":"rs1799734061","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140431608,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431608,"source":"dbSNP"},{"id":"rs1799734094","seq_region_name":"7","clinical_significance":[],"alleles":["A","G"],"end":140431611,"strand":1,"feature_type":"variation","start":140431611,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"id":"rs1799734112","seq_region_name":"7","source":"dbSNP","start":140431613,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140431613,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1382577304","clinical_significance":[],"start":140431614,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140431614,"strand":1,"feature_type":"variation"},{"id":"rs1459314483","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140431615,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431615,"source":"dbSNP"},{"clinical_significance":[],"id":"rs2130189691","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431615,"feature_type":"variation","strand":1,"end":140431619,"alleles":["TCTCT","TCT"]},{"strand":1,"feature_type":"variation","end":140431616,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431616,"source":"dbSNP","seq_region_name":"7","id":"rs2130189697","clinical_significance":[]},{"seq_region_name":"7","id":"rs1004378769","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C","T"],"end":140431620,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431620,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1374844734","seq_region_name":"7","end":140431621,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140431621,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140431623,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431623,"clinical_significance":[],"seq_region_name":"7","id":"rs1295965529"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431624,"feature_type":"variation","strand":1,"end":140431624,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1440941143"},{"alleles":["C","CAAC"],"end":140431626,"strand":1,"feature_type":"variation","start":140431626,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1237700705","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431626,"source":"dbSNP","strand":1,"feature_type":"variation","end":140431672,"alleles":["CCGCCCCGTCTGAGAAGTGAGGAGACCCTCTGCCTGGCAACCGCCCC","CCGCCCC"],"seq_region_name":"7","id":"rs1554443642","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799734291","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431627,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140431627},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431628,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140431628,"seq_region_name":"7","id":"rs527588264","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431629,"feature_type":"variation","strand":1,"end":140431629,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799734331"},{"strand":1,"feature_type":"variation","alleles":["-","AT"],"end":140431631,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431632,"source":"dbSNP","seq_region_name":"7","id":"rs1799734344","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140431632,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431632,"clinical_significance":[],"seq_region_name":"7","id":"rs1190261848"},{"clinical_significance":[],"seq_region_name":"7","id":"rs371088409","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431633,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140431633},{"feature_type":"variation","strand":1,"alleles":["TCTGAGAAGTGAGGAGACCCTCTGCCTGGCAACCGCCCCATCTGAGAAGTGAG","TCTGAGAAGTGAG"],"end":140431686,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431634,"clinical_significance":[],"seq_region_name":"7","id":"rs1563078174"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585442192","end":140431638,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140431638,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1585442196","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140431641,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431641,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799734486","clinical_significance":[],"alleles":["G","A"],"end":140431646,"strand":1,"feature_type":"variation","start":140431646,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1420832597","feature_type":"variation","strand":1,"end":140431647,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431647},{"start":140431650,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","C","G"],"end":140431650,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1248460285","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1490557790","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140431651,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431651},{"clinical_significance":[],"id":"rs1799734551","seq_region_name":"7","alleles":["CCCTCTGCCTGGCAACCGCCCCATCTGAGAAGTGAGAAGCCCCTC","CCCTC"],"end":140431695,"feature_type":"variation","strand":1,"source":"dbSNP","start":140431651,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140431652,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431652,"source":"dbSNP","id":"rs1799734565","seq_region_name":"7","clinical_significance":[]},{"id":"rs1271302399","seq_region_name":"7","clinical_significance":[],"start":140431656,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140431656,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1220623029","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140431660,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431660,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1236162664","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431661,"feature_type":"variation","strand":1,"alleles":["GGCAACCGCCCCATCTGAGAAGTGAGAAGCCCCTCCGCCCGGCA","GGCA"],"end":140431704},{"seq_region_name":"7","id":"rs1359128413","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["CAAC","C"],"end":140431666,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431663,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431664,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140431664,"seq_region_name":"7","id":"rs1261726766","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140431665,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431665,"source":"dbSNP","id":"rs1241738577","seq_region_name":"7","clinical_significance":[]},{"id":"rs1315667766","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431667,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140431667},{"source":"dbSNP","start":140431668,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140431668,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1304164718"},{"end":140431670,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140431670,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1227236207"},{"seq_region_name":"7","id":"rs1345670970","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140431671,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431671,"source":"dbSNP"},{"start":140431673,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140431673,"alleles":["A","G"],"strand":1,"feature_type":"variation","id":"rs1304549330","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1472682150","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431674,"feature_type":"variation","strand":1,"alleles":["TCTGAGAAGTGAGAAGCCCCTCCGCCCGGCAGCCACCCCGTCTGAGAAGTGAG","TCTGAGAAGTGAG"],"end":140431726},{"source":"dbSNP","start":140431675,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140431675,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs182906708","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140431677,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431677,"clinical_significance":[],"seq_region_name":"7","id":"rs1402771564"},{"id":"rs1168912111","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431679,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140431679},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431681,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140431681,"seq_region_name":"7","id":"rs2130189791","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1289263526","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431684,"feature_type":"variation","strand":1,"end":140431684,"alleles":["G","A"]},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140431687,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431687,"source":"dbSNP","seq_region_name":"7","id":"rs1455221723","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1422089127","alleles":["AGCCCCTCCGCCCGGCAGCCACCCCGTCTGAGAAGTGAGGAGCCCCTCCGCCCGGCAGCCACCCCGTC","AGCCCCTCCGCCCGGCAGCCACCCCGTC"],"end":140431755,"feature_type":"variation","strand":1,"source":"dbSNP","start":140431688,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1463768291","clinical_significance":[],"end":140431689,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140431689,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1431587356","source":"dbSNP","start":140431690,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140431690,"alleles":["C","A"],"feature_type":"variation","strand":1},{"end":140431693,"alleles":["CCCC","CCC"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140431690,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1480801997"},{"clinical_significance":[],"id":"rs1799734985","seq_region_name":"7","end":140431691,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140431691,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"end":140431692,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140431692,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799735006","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431695,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140431695,"seq_region_name":"7","id":"rs1799735018","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140431696,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431696,"source":"dbSNP","seq_region_name":"7","id":"rs1197504461","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["CGCCCGGCAGCCACCCCG","-"],"end":140431713,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431696,"clinical_significance":[],"id":"rs1799735047","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140431697,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431697,"clinical_significance":[],"seq_region_name":"7","id":"rs539311157"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1207278166","alleles":["C","T"],"end":140431698,"feature_type":"variation","strand":1,"source":"dbSNP","start":140431698,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1485132004","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","A","G","T"],"end":140431700,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431700},{"strand":1,"feature_type":"variation","end":140431713,"alleles":["CGGCAGCCACCCCG","-"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431700,"source":"dbSNP","seq_region_name":"7","id":"rs2130189828","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799735133","clinical_significance":[],"start":140431701,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140431701,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1224711001","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431704,"feature_type":"variation","strand":1,"end":140431704,"alleles":["A","C"]},{"source":"dbSNP","start":140431705,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140431705,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1406196208","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1454058914","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431708,"feature_type":"variation","strand":1,"end":140431708,"alleles":["A","G"]},{"alleles":["C","A"],"end":140431709,"strand":1,"feature_type":"variation","start":140431709,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799735208","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799735243","clinical_significance":[],"start":140431710,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140431710,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140431713,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431713,"source":"dbSNP","id":"rs1332136448","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799735292","source":"dbSNP","start":140431714,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140431714,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140431740,"alleles":["CTGAGAAGTGAGGAGCCCCTCCGCCC","-"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431715,"source":"dbSNP","id":"rs2130189859","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431716,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140431716,"clinical_significance":[],"seq_region_name":"7","id":"rs1250823243"},{"source":"dbSNP","start":140431718,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140431718,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1431388859"},{"strand":1,"feature_type":"variation","end":140431718,"alleles":["A","-"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431718,"source":"dbSNP","seq_region_name":"7","id":"rs1799735361","clinical_significance":[]},{"id":"rs1799735385","seq_region_name":"7","clinical_significance":[],"end":140431720,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140431720,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140431721,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431721,"source":"dbSNP","seq_region_name":"7","id":"rs1799735403","clinical_significance":[]},{"end":140431723,"alleles":["T","C","G"],"strand":1,"feature_type":"variation","start":140431723,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799735425","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431725,"feature_type":"variation","strand":1,"end":140431725,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799735450"},{"id":"rs1383691741","seq_region_name":"7","clinical_significance":[],"start":140431727,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140431727,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799735498","feature_type":"variation","strand":1,"alleles":["-","TGGGGGTC"],"end":140431727,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431728},{"clinical_significance":[],"id":"rs1382596694","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140431731,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431731},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431732,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140431732,"clinical_significance":[],"seq_region_name":"7","id":"rs1288183544"},{"seq_region_name":"7","id":"rs1799735562","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140431733,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431733,"source":"dbSNP"},{"end":140431734,"alleles":["T","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140431734,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799735575"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1760732452","alleles":["CC","C"],"end":140431736,"feature_type":"variation","strand":1,"source":"dbSNP","start":140431735,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431736,"source":"dbSNP","strand":1,"feature_type":"variation","end":140431736,"alleles":["C","T"],"seq_region_name":"7","id":"rs1271758114","clinical_significance":[]},{"seq_region_name":"7","id":"rs552485732","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140431737,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431737,"source":"dbSNP"},{"id":"rs1174405550","seq_region_name":"7","clinical_significance":[],"start":140431738,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140431738,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"end":140431739,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140431739,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799735740"},{"clinical_significance":[],"id":"rs1480200953","seq_region_name":"7","feature_type":"variation","strand":1,"end":140431740,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431740},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431741,"source":"dbSNP","strand":1,"feature_type":"variation","end":140431740,"alleles":["-","A"],"seq_region_name":"7","id":"rs1799735786","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140431741,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431741,"source":"dbSNP","id":"rs1373848839","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140431742,"alleles":["G","A","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431742,"clinical_significance":[],"id":"rs1195692013","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1217059451","source":"dbSNP","start":140431743,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","CC"],"end":140431743,"feature_type":"variation","strand":1},{"alleles":["C","G"],"end":140431743,"strand":1,"feature_type":"variation","start":140431743,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1585442263","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","C"],"end":140431744,"feature_type":"variation","strand":1,"source":"dbSNP","start":140431744,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799735877"},{"seq_region_name":"7","id":"rs1585442267","clinical_significance":[],"start":140431745,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A","C"],"end":140431745,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140431747,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140431747,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799735925"},{"id":"rs746015625","seq_region_name":"7","clinical_significance":[],"start":140431748,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140431748,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1585442278","seq_region_name":"7","feature_type":"variation","strand":1,"end":140431749,"alleles":["C","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431749},{"feature_type":"variation","strand":1,"end":140431809,"alleles":["CCCCGTCCGGGAGGGAGGTGGGGGTCAGCCCCCCGCCCGGCCAGCTGCCCCGTCCGGGAGG","CCCCGTCCGGGAGG"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431749,"clinical_significance":[],"seq_region_name":"7","id":"rs1799736002"},{"end":140431750,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140431750,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1202190599"},{"end":140431751,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140431751,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799736048","clinical_significance":[]},{"start":140431752,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140431752,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","id":"rs1442414883","seq_region_name":"7","clinical_significance":[]},{"start":140431753,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A","C"],"end":140431753,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1219773723","clinical_significance":[]},{"source":"dbSNP","start":140431754,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140431754,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799736123"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431756,"feature_type":"variation","strand":1,"end":140431756,"alleles":["C","G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1265854353"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1201243375","source":"dbSNP","start":140431757,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140431757,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1343742158","clinical_significance":[],"strand":1,"feature_type":"variation","end":140431757,"alleles":["-","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431758,"source":"dbSNP"},{"end":140431759,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140431759,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs774753433","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1192517515","source":"dbSNP","start":140431760,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","C","G"],"end":140431760,"feature_type":"variation","strand":1},{"alleles":["A","AA"],"end":140431760,"feature_type":"variation","strand":1,"source":"dbSNP","start":140431760,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130189968"},{"strand":1,"feature_type":"variation","end":140431761,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431761,"source":"dbSNP","seq_region_name":"7","id":"rs1229204580","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140431762,"alleles":["G","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431762,"clinical_significance":[],"id":"rs1429488369","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431764,"source":"dbSNP","strand":1,"feature_type":"variation","end":140431764,"alleles":["A","G"],"seq_region_name":"7","id":"rs1467252326","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799736331","clinical_significance":[],"strand":1,"feature_type":"variation","end":140431765,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431765,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1585442313","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140431766,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431766},{"end":140431767,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140431767,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs866932764"},{"strand":1,"feature_type":"variation","alleles":["TGGGGGTC","-"],"end":140431774,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431767,"source":"dbSNP","seq_region_name":"7","id":"rs1296622070","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["-","TG"],"end":140431767,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431768,"source":"dbSNP","seq_region_name":"7","id":"rs1799736415","clinical_significance":[]},{"source":"dbSNP","start":140431768,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["GGGGG","GGGGGG","GGGGGGG","GGGGGGGG"],"end":140431772,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1384910169"},{"feature_type":"variation","strand":1,"end":140431793,"alleles":["GGGGGTCAGCCCCCCGCCCGGCCAGC","GGGGGTCAGCCCCCCGCCCGGCCAGCCGCCCCGTCCGGAAGGGAGGTGGGGGGGTCAGCCCCCCGCCCGGCCAGC"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431768,"clinical_significance":[],"seq_region_name":"7","id":"rs1799736467"},{"seq_region_name":"7","id":"rs1799736481","clinical_significance":[],"start":140431769,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140431769,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"start":140431771,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","GAG"],"end":140431771,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585442320","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799736562","seq_region_name":"7","source":"dbSNP","start":140431771,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140431771,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140431774,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431774,"source":"dbSNP","seq_region_name":"7","id":"rs1413977029","clinical_significance":[]},{"source":"dbSNP","start":140431775,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140431775,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799736610"},{"start":140431776,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140431776,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799736627","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799736640","alleles":["G","-"],"end":140431776,"feature_type":"variation","strand":1,"source":"dbSNP","start":140431776,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799736661","source":"dbSNP","start":140431777,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140431777,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431777,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CCCCCC","CCCCC","CCCCCCC"],"end":140431782,"seq_region_name":"7","id":"rs1170368784","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431778,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140431778,"clinical_significance":[],"seq_region_name":"7","id":"rs1585442326"},{"strand":1,"feature_type":"variation","alleles":["CCCCCGCCCGGCC","CC"],"end":140431790,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431778,"source":"dbSNP","seq_region_name":"7","id":"rs1049680684","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431780,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140431780,"seq_region_name":"7","id":"rs1799736749","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1400836826","feature_type":"variation","strand":1,"end":140431782,"alleles":["C","A","G","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431782},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799736797","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431783,"feature_type":"variation","strand":1,"alleles":["-","T"],"end":140431782},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431783,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140431783,"clinical_significance":[],"seq_region_name":"7","id":"rs1401268859"},{"feature_type":"variation","strand":1,"alleles":["G","GG"],"end":140431783,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431783,"clinical_significance":[],"seq_region_name":"7","id":"rs1799736835"},{"seq_region_name":"7","id":"rs1320152174","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431786,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140431786},{"alleles":["G","A"],"end":140431787,"strand":1,"feature_type":"variation","start":140431787,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1338186357","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1399094397","seq_region_name":"7","end":140431788,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140431788,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140431791,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140431791,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1241819690"},{"alleles":["A","-"],"end":140431791,"strand":1,"feature_type":"variation","start":140431791,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1799736936","seq_region_name":"7","clinical_significance":[]},{"end":140431792,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140431792,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1277820146","clinical_significance":[]},{"end":140431793,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140431793,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799736977"},{"start":140431794,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","A","C"],"end":140431794,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs867732237","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431795,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140431795,"seq_region_name":"7","id":"rs1235689669","clinical_significance":[]},{"seq_region_name":"7","id":"rs1254377134","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431797,"source":"dbSNP","strand":1,"feature_type":"variation","end":140431797,"alleles":["C","A","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1344368357","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431798,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140431798},{"seq_region_name":"7","id":"rs1337072224","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140431799,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431799,"source":"dbSNP"},{"source":"dbSNP","start":140431800,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140431800,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1206259510"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799737166","source":"dbSNP","start":140431800,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","GG"],"end":140431800,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1246452397","clinical_significance":[],"start":140431801,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140431801,"strand":1,"feature_type":"variation"},{"end":140431803,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140431803,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1451842482","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1288729311","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431804,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140431804},{"start":140431804,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["GG","GGAAGG"],"end":140431805,"strand":1,"feature_type":"variation","id":"rs1799737264","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130190120","end":140431809,"alleles":["GGGAGG","GGGAGGGAGG"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140431804,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"id":"rs1799737276","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140431805,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431805,"source":"dbSNP"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431806,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140431806,"clinical_significance":[],"seq_region_name":"7","id":"rs1487522688"},{"start":140431807,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","T"],"end":140431807,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799737317","clinical_significance":[]},{"alleles":["G","A"],"end":140431808,"strand":1,"feature_type":"variation","start":140431808,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1799737337","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431809,"source":"dbSNP","strand":1,"feature_type":"variation","end":140431809,"alleles":["G","T"],"seq_region_name":"7","id":"rs1447271054","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431810,"source":"dbSNP","strand":1,"feature_type":"variation","end":140431810,"alleles":["T","-"],"seq_region_name":"7","id":"rs1216425392","clinical_significance":[]},{"seq_region_name":"7","id":"rs1270048372","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431810,"source":"dbSNP","strand":1,"feature_type":"variation","end":140431810,"alleles":["T","G"]},{"seq_region_name":"7","id":"rs1434589747","clinical_significance":[],"strand":1,"feature_type":"variation","end":140431812,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431812,"source":"dbSNP"},{"end":140431815,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140431815,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799737418","clinical_significance":[]},{"start":140431816,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140431816,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799737433","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1196282275","alleles":["C","A","T"],"end":140431817,"feature_type":"variation","strand":1,"source":"dbSNP","start":140431817,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1376600042","source":"dbSNP","start":140431818,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A","C","T"],"end":140431818,"feature_type":"variation","strand":1},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431819,"feature_type":"variation","strand":1,"alleles":["CCTCTGCCCGGCCGCCCCTACTGGGAAGTGAGGAGCCCCTCTGCCCGGCC","CCTCTGCCCGGCC"],"end":140431868,"clinical_significance":[],"id":"rs1799737518","seq_region_name":"7"},{"alleles":["C","T"],"end":140431820,"feature_type":"variation","strand":1,"source":"dbSNP","start":140431820,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799737541"},{"feature_type":"variation","strand":1,"end":140431822,"alleles":["C","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431822,"clinical_significance":[],"seq_region_name":"7","id":"rs1799737563"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1470164044","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140431826,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431826},{"start":140431827,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","A","T"],"end":140431827,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1160390429","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A","C","T"],"end":140431828,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431828,"source":"dbSNP","seq_region_name":"7","id":"rs1358482381","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1383820778","alleles":["C","A"],"end":140431830,"feature_type":"variation","strand":1,"source":"dbSNP","start":140431830,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140431831,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431831,"source":"dbSNP","seq_region_name":"7","id":"rs1419007884","clinical_significance":[]},{"id":"rs1470809339","seq_region_name":"7","clinical_significance":[],"alleles":["G","A","T"],"end":140431832,"strand":1,"feature_type":"variation","start":140431832,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"source":"dbSNP","start":140431834,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140431834,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799737720"},{"id":"rs1799737739","seq_region_name":"7","clinical_significance":[],"alleles":["C","A","T"],"end":140431836,"strand":1,"feature_type":"variation","start":140431836,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1232908972","clinical_significance":[],"start":140431837,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","G"],"end":140431837,"strand":1,"feature_type":"variation"},{"alleles":["A","C","G","T"],"end":140431838,"feature_type":"variation","strand":1,"source":"dbSNP","start":140431838,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1183356181"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431839,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140431839,"clinical_significance":[],"seq_region_name":"7","id":"rs1435654604"},{"start":140431840,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","G"],"end":140431840,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1303605600","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431841,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140431841,"clinical_significance":[],"seq_region_name":"7","id":"rs1799737854"},{"start":140431843,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140431843,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs112822626","clinical_significance":[]},{"start":140431845,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140431845,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1222827372","clinical_significance":[]},{"seq_region_name":"7","id":"rs1490774085","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140431846,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431846,"source":"dbSNP"},{"id":"rs1799737926","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431847,"source":"dbSNP","strand":1,"feature_type":"variation","end":140431847,"alleles":["T","A","C"]},{"start":140431851,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140431851,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799737946","clinical_significance":[]},{"source":"dbSNP","start":140431854,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140431854,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1289355975"},{"seq_region_name":"7","id":"rs1367171164","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["CCCC","CCC"],"end":140431857,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431854,"source":"dbSNP"},{"id":"rs2130190224","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431856,"source":"dbSNP","strand":1,"feature_type":"variation","end":140431856,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1799737996","clinical_significance":[],"start":140431857,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140431857,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"end":140431860,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140431860,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799738018"},{"seq_region_name":"7","id":"rs1388791162","clinical_significance":[],"start":140431864,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140431864,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431865,"feature_type":"variation","strand":1,"end":140431865,"alleles":["G","A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1351317410"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1236959115","alleles":["G","A"],"end":140431866,"feature_type":"variation","strand":1,"source":"dbSNP","start":140431866,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140431867,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140431867,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799738104","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1680562144","seq_region_name":"7","source":"dbSNP","start":140431868,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140431868,"feature_type":"variation","strand":1},{"alleles":["A","G"],"end":140431869,"feature_type":"variation","strand":1,"source":"dbSNP","start":140431869,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs570666633","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1799738153","seq_region_name":"7","source":"dbSNP","start":140431870,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140431870,"alleles":["C","G","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1303950564","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431870,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CC","C"],"end":140431871},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431871,"feature_type":"variation","strand":1,"end":140431871,"alleles":["C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1330625779"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799738205","end":140431873,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140431873,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["CCCC","CC"],"end":140431876,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431873,"source":"dbSNP","seq_region_name":"7","id":"rs1799738224","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431875,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140431875,"seq_region_name":"7","id":"rs1239770534","clinical_significance":[]},{"seq_region_name":"7","id":"rs1364053534","clinical_significance":[],"start":140431875,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["CCGTCTGGGA","-"],"end":140431884,"strand":1,"feature_type":"variation"},{"id":"rs1311543178","seq_region_name":"7","clinical_significance":[],"end":140431876,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140431876,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1352244718","clinical_significance":[],"end":140431877,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140431877,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"id":"rs1157395483","seq_region_name":"7","clinical_significance":[],"start":140431880,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","A","C"],"end":140431880,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1216486816","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431885,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140431885},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431886,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140431886,"seq_region_name":"7","id":"rs1410652853","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140431888,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431888,"source":"dbSNP","seq_region_name":"7","id":"rs1799738399","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1293023616","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431889,"feature_type":"variation","strand":1,"end":140431889,"alleles":["T","C"]},{"start":140431890,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140431890,"alleles":["A","G"],"strand":1,"feature_type":"variation","id":"rs1489644164","seq_region_name":"7","clinical_significance":[]},{"end":140431892,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140431892,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1207735657"},{"source":"dbSNP","start":140431897,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140431897,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799738487"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130190321","source":"dbSNP","start":140431902,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140431902,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1799738506","clinical_significance":[],"strand":1,"feature_type":"variation","end":140431903,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431903,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140431905,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431905,"clinical_significance":[],"seq_region_name":"7","id":"rs900929466"},{"clinical_significance":[],"id":"rs1799738539","seq_region_name":"7","alleles":["A","-"],"end":140431906,"feature_type":"variation","strand":1,"source":"dbSNP","start":140431906,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1447424813","source":"dbSNP","start":140431907,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140431907,"alleles":["G","A"],"feature_type":"variation","strand":1},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431909,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140431909,"clinical_significance":[],"seq_region_name":"7","id":"rs1799738571"},{"seq_region_name":"7","id":"rs1266148571","clinical_significance":[],"alleles":["A","C","G","T"],"end":140431911,"strand":1,"feature_type":"variation","start":140431911,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"source":"dbSNP","start":140431916,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140431916,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs996660259"},{"seq_region_name":"7","id":"rs1437918953","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431917,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140431917},{"id":"rs1799738657","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140431920,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431920,"source":"dbSNP"},{"end":140431923,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140431923,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799738679","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799738704","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431924,"source":"dbSNP","strand":1,"feature_type":"variation","end":140431924,"alleles":["A","G"]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431929,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140431929,"clinical_significance":[],"id":"rs1180032769","seq_region_name":"7"},{"end":140431929,"alleles":["C","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140431929,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799738739","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1377942276","feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140431930,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431930},{"end":140431931,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140431931,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1225534135","clinical_significance":[]},{"alleles":["T","C","G"],"end":140431932,"strand":1,"feature_type":"variation","start":140431932,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1274568087","clinical_significance":[]},{"start":140431932,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140431935,"alleles":["TTTT","TTTTT"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1439050093","clinical_significance":[]},{"end":140431933,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140431933,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1164106629","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799738846","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140431934,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431934},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585442443","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140431936,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431936},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431940,"feature_type":"variation","strand":1,"end":140431940,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585442445"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431941,"feature_type":"variation","strand":1,"end":140431941,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1028102438"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799738969","feature_type":"variation","strand":1,"end":140431942,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431942},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431947,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140431947,"clinical_significance":[],"seq_region_name":"7","id":"rs1456159939"},{"source":"dbSNP","start":140431948,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140431948,"alleles":["G","A","C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1292002594","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1316824048","clinical_significance":[],"start":140431948,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140431953,"alleles":["GGGGGG","GGGGG","GGGGGGG"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["G","A","C","T"],"end":140431949,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431949,"source":"dbSNP","seq_region_name":"7","id":"rs1390366947","clinical_significance":[]},{"seq_region_name":"7","id":"rs968622320","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431950,"source":"dbSNP","strand":1,"feature_type":"variation","end":140431950,"alleles":["G","A","C","T"]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431952,"source":"dbSNP","strand":1,"feature_type":"variation","end":140431952,"alleles":["G","A"],"seq_region_name":"7","id":"rs1799739114","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799739137","clinical_significance":[],"strand":1,"feature_type":"variation","end":140431954,"alleles":["GA","-"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431953,"source":"dbSNP"},{"alleles":["A","G"],"end":140431954,"feature_type":"variation","strand":1,"source":"dbSNP","start":140431954,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1475599733"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585442466","source":"dbSNP","start":140431955,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140431955,"alleles":["A","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1000092406","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431956,"source":"dbSNP","strand":1,"feature_type":"variation","end":140431956,"alleles":["A","G"]},{"id":"rs1374737832","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431957,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140431957},{"clinical_significance":[],"seq_region_name":"7","id":"rs1240092170","feature_type":"variation","strand":1,"end":140431959,"alleles":["T","C","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431959},{"strand":1,"feature_type":"variation","end":140431961,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431961,"source":"dbSNP","seq_region_name":"7","id":"rs1799739237","clinical_significance":[]},{"end":140431964,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140431964,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs2130190422","clinical_significance":[]},{"end":140431967,"alleles":["AAAA","AA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140431964,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs575460415"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799739275","end":140431967,"alleles":["A","C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140431967,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799739297","end":140431970,"alleles":["AGAT","AGATAGAT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140431967,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431968,"source":"dbSNP","strand":1,"feature_type":"variation","end":140431968,"alleles":["G","A"],"seq_region_name":"7","id":"rs1799739319","clinical_significance":[]},{"clinical_significance":[],"id":"rs1464408380","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431969,"feature_type":"variation","strand":1,"end":140431976,"alleles":["ATTGAGAA","A"]},{"strand":1,"feature_type":"variation","end":140431970,"alleles":["T","A","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431970,"source":"dbSNP","id":"rs1263761311","seq_region_name":"7","clinical_significance":[]},{"id":"rs1323884457","seq_region_name":"7","clinical_significance":[],"alleles":["TT","-"],"end":140431971,"strand":1,"feature_type":"variation","start":140431970,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799739382","feature_type":"variation","strand":1,"end":140431971,"alleles":["T","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431971},{"source":"dbSNP","start":140431972,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140431972,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1242996579"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431973,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140431973,"seq_region_name":"7","id":"rs2130190463","clinical_significance":[]},{"clinical_significance":[],"id":"rs1265211579","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431974,"feature_type":"variation","strand":1,"end":140431978,"alleles":["GAAAT","-"]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431974,"feature_type":"variation","strand":1,"alleles":["GAAATCGGATGGTTGCCGTGTCTGTG","G"],"end":140431999,"clinical_significance":[],"seq_region_name":"7","id":"rs1205661264"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799739457","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431975,"feature_type":"variation","strand":1,"end":140431977,"alleles":["AAA","AA"]},{"seq_region_name":"7","id":"rs1032090551","clinical_significance":[],"alleles":["A","C","G"],"end":140431977,"strand":1,"feature_type":"variation","start":140431977,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1215432473","clinical_significance":[],"alleles":["T","A"],"end":140431978,"strand":1,"feature_type":"variation","start":140431978,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs4617068","source":"dbSNP","start":140431979,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140431979,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1799739556","clinical_significance":[],"strand":1,"feature_type":"variation","end":140431980,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431980,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1200104692","end":140431981,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140431981,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1799739610","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140431982,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431982,"source":"dbSNP"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431984,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140431984,"clinical_significance":[],"seq_region_name":"7","id":"rs956033809"},{"seq_region_name":"7","id":"rs1799739657","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431986,"source":"dbSNP","strand":1,"feature_type":"variation","end":140431986,"alleles":["T","C"]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431990,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140431990,"seq_region_name":"7","id":"rs1339343498","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140431991,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140431991,"source":"dbSNP","seq_region_name":"7","id":"rs993230497","clinical_significance":[]},{"clinical_significance":[],"id":"rs550024628","seq_region_name":"7","alleles":["T","G"],"end":140431992,"feature_type":"variation","strand":1,"source":"dbSNP","start":140431992,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1410202607","seq_region_name":"7","feature_type":"variation","strand":1,"end":140431995,"alleles":["C","G","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431995},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140431999,"feature_type":"variation","strand":1,"end":140431999,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1186451582"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432000,"feature_type":"variation","strand":1,"end":140432000,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799739777"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1448733912","end":140432001,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140432001,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432004,"source":"dbSNP","strand":1,"feature_type":"variation","end":140432004,"alleles":["A","G","T"],"id":"rs1243662768","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432004,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AAGAAG","AAG"],"end":140432009,"id":"rs1456891602","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130190532","feature_type":"variation","strand":1,"end":140432006,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432006},{"seq_region_name":"7","id":"rs1799739856","clinical_significance":[],"start":140432007,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140432008,"alleles":["AA","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs568535829","clinical_significance":[],"start":140432008,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140432008,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432008,"feature_type":"variation","strand":1,"alleles":["AGTAG","AG"],"end":140432012,"clinical_significance":[],"seq_region_name":"7","id":"rs1185412419"},{"seq_region_name":"7","id":"rs1237001176","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432010,"source":"dbSNP","strand":1,"feature_type":"variation","end":140432010,"alleles":["T","G"]},{"feature_type":"variation","strand":1,"alleles":["TA","-"],"end":140432011,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432010,"clinical_significance":[],"id":"rs1799739941","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1205439212","clinical_significance":[],"start":140432011,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140432011,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1799739974","clinical_significance":[],"start":140432013,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140432013,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1799739994","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432015,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140432015},{"id":"rs1258095439","seq_region_name":"7","clinical_significance":[],"alleles":["C","G"],"end":140432023,"strand":1,"feature_type":"variation","start":140432023,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799740029","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432024,"feature_type":"variation","strand":1,"alleles":["TTTT","TT"],"end":140432027},{"clinical_significance":[],"seq_region_name":"7","id":"rs917378929","source":"dbSNP","start":140432029,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140432029,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140432033,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432033,"clinical_significance":[],"seq_region_name":"7","id":"rs1163897912"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432034,"source":"dbSNP","strand":1,"feature_type":"variation","end":140432034,"alleles":["G","A","T"],"seq_region_name":"7","id":"rs1228112979","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585442526","source":"dbSNP","start":140432038,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140432038,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1799740145","clinical_significance":[],"end":140432039,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140432039,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"source":"dbSNP","start":140432040,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140432040,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799740166"},{"source":"dbSNP","start":140432042,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140432042,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1373403937"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1207893263","source":"dbSNP","start":140432044,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","C","G"],"end":140432044,"feature_type":"variation","strand":1},{"start":140432045,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140432045,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799740231","clinical_significance":[]},{"start":140432046,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140432046,"alleles":["G","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs970112926","clinical_significance":[]},{"end":140432047,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140432047,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799740276"},{"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140432048,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432048,"clinical_significance":[],"seq_region_name":"7","id":"rs1799740294"},{"id":"rs34499571","seq_region_name":"7","clinical_significance":[],"end":140432049,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140432049,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"alleles":["A","G"],"end":140432051,"feature_type":"variation","strand":1,"source":"dbSNP","start":140432051,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1446046165"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432052,"source":"dbSNP","strand":1,"feature_type":"variation","end":140432052,"alleles":["T","G"],"seq_region_name":"7","id":"rs1442393544","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799740385","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432052,"feature_type":"variation","strand":1,"end":140432058,"alleles":["TTCTTCT","TTCT"]},{"id":"rs368742276","seq_region_name":"7","clinical_significance":[],"end":140432058,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140432058,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs980295636","source":"dbSNP","start":140432060,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140432060,"alleles":["C","T"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432068,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140432068,"seq_region_name":"7","id":"rs1799740440","clinical_significance":[]},{"seq_region_name":"7","id":"rs1303948539","clinical_significance":[],"end":140432069,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140432069,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"id":"rs1585442547","seq_region_name":"7","clinical_significance":[],"start":140432072,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140432072,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs920732315","clinical_significance":[],"start":140432073,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140432073,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140432077,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["TCT","T"],"end":140432079,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1382039127"},{"seq_region_name":"7","id":"rs1385676024","clinical_significance":[],"alleles":["T","G"],"end":140432079,"strand":1,"feature_type":"variation","start":140432079,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1394796521","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432080,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140432080},{"clinical_significance":[],"seq_region_name":"7","id":"rs4590358","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432083,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140432083},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130190638","end":140432087,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140432087,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["ACCCCCAACCCTGTGCTCTC","ACCCCCAACCCTGTGCTCTCACCCCCAACCCTGTGCTCTC"],"end":140432107,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432088,"source":"dbSNP","seq_region_name":"7","id":"rs1799740614","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs371652712","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432089,"feature_type":"variation","strand":1,"end":140432089,"alleles":["C","T"]},{"feature_type":"variation","strand":1,"alleles":["CCCCC","CCCCCC"],"end":140432093,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432089,"clinical_significance":[],"seq_region_name":"7","id":"rs1799740666"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432090,"feature_type":"variation","strand":1,"end":140432090,"alleles":["C","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585442558"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432097,"source":"dbSNP","strand":1,"feature_type":"variation","end":140432097,"alleles":["C","A","T"],"seq_region_name":"7","id":"rs554183265","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432098,"feature_type":"variation","strand":1,"end":140432098,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799740716"},{"seq_region_name":"7","id":"rs1799740726","clinical_significance":[],"end":140432099,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140432099,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1177872439","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140432103,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432103,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1481694293","clinical_significance":[],"start":140432104,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","A","C","G"],"end":140432104,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1799740783","clinical_significance":[],"alleles":["C","T"],"end":140432105,"strand":1,"feature_type":"variation","start":140432105,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1220111294","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432106,"feature_type":"variation","strand":1,"end":140432106,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs572447328","alleles":["C","G"],"end":140432107,"feature_type":"variation","strand":1,"source":"dbSNP","start":140432107,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1204757299","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432114,"source":"dbSNP","strand":1,"feature_type":"variation","end":140432114,"alleles":["A","G"]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432114,"feature_type":"variation","strand":1,"end":140432115,"alleles":["AT","-"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799740857"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432115,"feature_type":"variation","strand":1,"alleles":["T","A","G"],"end":140432115,"clinical_significance":[],"seq_region_name":"7","id":"rs930893421"},{"start":140432116,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A","C"],"end":140432116,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1203677498","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1257243708","feature_type":"variation","strand":1,"end":140432117,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432117},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432118,"feature_type":"variation","strand":1,"end":140432118,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1243197950"},{"seq_region_name":"7","id":"rs1321643038","clinical_significance":[],"end":140432119,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140432119,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"start":140432131,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","C"],"end":140432131,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs539733496","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1223838824","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432133,"feature_type":"variation","strand":1,"end":140432133,"alleles":["G","A"]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432135,"source":"dbSNP","strand":1,"feature_type":"variation","end":140432135,"alleles":["T","A"],"seq_region_name":"7","id":"rs1799741007","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432137,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140432137,"clinical_significance":[],"seq_region_name":"7","id":"rs3929581"},{"alleles":["A","G"],"end":140432139,"strand":1,"feature_type":"variation","start":140432139,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799741059","clinical_significance":[]},{"start":140432140,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140432140,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs367661923","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799741095","source":"dbSNP","start":140432143,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140432143,"feature_type":"variation","strand":1},{"id":"rs1799741108","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432147,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140432147},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140432151,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432151,"clinical_significance":[],"id":"rs6969624","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432152,"source":"dbSNP","strand":1,"feature_type":"variation","end":140432152,"alleles":["G","C"],"id":"rs1408865731","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140432155,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432155,"clinical_significance":[],"seq_region_name":"7","id":"rs1365922335"},{"feature_type":"variation","strand":1,"end":140432156,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432156,"clinical_significance":[],"seq_region_name":"7","id":"rs1799741186"},{"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140432159,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432159,"source":"dbSNP","seq_region_name":"7","id":"rs1430627118","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432161,"source":"dbSNP","strand":1,"feature_type":"variation","end":140432161,"alleles":["T","C"],"seq_region_name":"7","id":"rs1304735534","clinical_significance":[]},{"end":140432164,"alleles":["TGTG","TG"],"strand":1,"feature_type":"variation","start":140432161,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1799741242","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140432164,"alleles":["G","A","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432164,"clinical_significance":[],"id":"rs1196123736","seq_region_name":"7"},{"end":140432166,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140432166,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799741273"},{"feature_type":"variation","strand":1,"end":140432169,"alleles":["G","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432169,"clinical_significance":[],"seq_region_name":"7","id":"rs1456275987"},{"end":140432175,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140432175,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs867085453","clinical_significance":[]},{"source":"dbSNP","start":140432176,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","C","T"],"end":140432176,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799741377"},{"id":"rs1159831499","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432181,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140432181},{"seq_region_name":"7","id":"rs1420927347","clinical_significance":[],"alleles":["G","T"],"end":140432184,"strand":1,"feature_type":"variation","start":140432184,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432188,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140432188,"seq_region_name":"7","id":"rs543581267","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432189,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140432189,"seq_region_name":"7","id":"rs1047941213","clinical_significance":[]},{"seq_region_name":"7","id":"rs573182405","clinical_significance":[],"start":140432191,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","C"],"end":140432191,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1799741504","clinical_significance":[],"strand":1,"feature_type":"variation","end":140432193,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432193,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1465024986","source":"dbSNP","start":140432194,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140432194,"alleles":["T","A","G"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140432195,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140432195,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1208440402","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130190821","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432196,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140432196},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432198,"feature_type":"variation","strand":1,"end":140432198,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799741530"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432199,"source":"dbSNP","strand":1,"feature_type":"variation","end":140432199,"alleles":["C","A","G","T"],"seq_region_name":"7","id":"rs3929582","clinical_significance":[]},{"id":"rs2130190839","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140432201,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432201,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799741591","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432207,"feature_type":"variation","strand":1,"end":140432207,"alleles":["T","A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs908111602","source":"dbSNP","start":140432208,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140432208,"alleles":["C","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1330575744","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432209,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140432209},{"seq_region_name":"7","id":"rs540605105","clinical_significance":[],"end":140432211,"alleles":["C","A","G","T"],"strand":1,"feature_type":"variation","start":140432211,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799741655","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432211,"feature_type":"variation","strand":1,"alleles":["C","-"],"end":140432211},{"clinical_significance":[],"seq_region_name":"7","id":"rs369692630","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432212,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140432212},{"seq_region_name":"7","id":"rs1799741704","clinical_significance":[],"alleles":["C","T"],"end":140432214,"strand":1,"feature_type":"variation","start":140432214,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"alleles":["C","G","T"],"end":140432216,"feature_type":"variation","strand":1,"source":"dbSNP","start":140432216,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1284868561"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799741732","alleles":["C","G"],"end":140432220,"feature_type":"variation","strand":1,"source":"dbSNP","start":140432220,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"end":140432227,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140432227,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1384860564","seq_region_name":"7"},{"source":"dbSNP","start":140432234,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","A","G"],"end":140432234,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799741857"},{"start":140432237,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140432237,"alleles":["G","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799741873","clinical_significance":[]},{"start":140432238,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140432238,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799741890","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585442632","feature_type":"variation","strand":1,"end":140432239,"alleles":["G","A","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432239},{"seq_region_name":"7","id":"rs904235162","clinical_significance":[],"alleles":["A","G"],"end":140432242,"strand":1,"feature_type":"variation","start":140432242,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1799741933","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432244,"source":"dbSNP","strand":1,"feature_type":"variation","end":140432246,"alleles":["AAA","AAAA"]},{"alleles":["T","A","G"],"end":140432251,"strand":1,"feature_type":"variation","start":140432251,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs3929583","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432252,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140432252,"clinical_significance":[],"id":"rs935659153","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1052829685","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432253,"feature_type":"variation","strand":1,"end":140432253,"alleles":["G","A","C"]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432254,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140432254,"seq_region_name":"7","id":"rs1799742048","clinical_significance":[]},{"alleles":["A","G"],"end":140432256,"feature_type":"variation","strand":1,"source":"dbSNP","start":140432256,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1219419749"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432259,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CC","C"],"end":140432260,"seq_region_name":"7","id":"rs1799742077","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1158521905","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432260,"feature_type":"variation","strand":1,"end":140432260,"alleles":["C","A","T"]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432261,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140432261,"clinical_significance":[],"seq_region_name":"7","id":"rs1302838805"},{"start":140432262,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140432262,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1431698574","clinical_significance":[]},{"alleles":["A","G"],"end":140432263,"strand":1,"feature_type":"variation","start":140432263,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1799742147","seq_region_name":"7","clinical_significance":[]},{"end":140432265,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140432265,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1197108387"},{"seq_region_name":"7","id":"rs900957252","clinical_significance":[],"start":140432266,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","T"],"end":140432266,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1799742211","clinical_significance":[],"strand":1,"feature_type":"variation","end":140432269,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432269,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140432275,"alleles":["C","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432275,"clinical_significance":[],"id":"rs1799742227","seq_region_name":"7"},{"id":"rs2130190944","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140432277,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432277,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140432283,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432283,"source":"dbSNP","id":"rs1262925277","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140432286,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","AA"],"end":140432286,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1188764866"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432290,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140432290,"clinical_significance":[],"id":"rs1209377772","seq_region_name":"7"},{"source":"dbSNP","start":140432292,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140432292,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799742311"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799742335","source":"dbSNP","start":140432294,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140432294,"feature_type":"variation","strand":1},{"end":140432307,"alleles":["TTGTTT","TT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140432302,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1265633631"},{"end":140432309,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140432309,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799742370","clinical_significance":[]},{"source":"dbSNP","start":140432310,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140432310,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1207542358","seq_region_name":"7"},{"alleles":["T","G"],"end":140432314,"feature_type":"variation","strand":1,"source":"dbSNP","start":140432314,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1323710915","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140432322,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432322,"clinical_significance":[],"seq_region_name":"7","id":"rs1211332729"},{"seq_region_name":"7","id":"rs1585442668","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140432324,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432324,"source":"dbSNP"},{"seq_region_name":"7","id":"rs996521608","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432327,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["ACTA","A"],"end":140432330},{"clinical_significance":[],"id":"rs1799742483","seq_region_name":"7","end":140432330,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140432330,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799742497","alleles":["T","C"],"end":140432332,"feature_type":"variation","strand":1,"source":"dbSNP","start":140432332,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs2130190985","clinical_significance":[],"alleles":["T","C"],"end":140432334,"strand":1,"feature_type":"variation","start":140432334,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"start":140432335,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140432335,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799742509","clinical_significance":[]},{"start":140432338,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140432338,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1049570020","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799742550","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432340,"source":"dbSNP","strand":1,"feature_type":"variation","end":140432340,"alleles":["G","T"]},{"source":"dbSNP","start":140432342,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140432342,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799742566"},{"clinical_significance":[],"id":"rs1585442674","seq_region_name":"7","source":"dbSNP","start":140432352,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140432352,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1799742595","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432354,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140432354},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140432356,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432356,"source":"dbSNP","seq_region_name":"7","id":"rs1799742615","clinical_significance":[]},{"id":"rs1296061683","seq_region_name":"7","clinical_significance":[],"alleles":["T","-"],"end":140432358,"strand":1,"feature_type":"variation","start":140432358,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"strand":1,"feature_type":"variation","end":140432358,"alleles":["T","A","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432358,"source":"dbSNP","seq_region_name":"7","id":"rs1585442675","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1437101307","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432361,"feature_type":"variation","strand":1,"end":140432361,"alleles":["G","T"]},{"seq_region_name":"7","id":"rs375927979","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140432362,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432362,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1362955308","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432362,"source":"dbSNP","strand":1,"feature_type":"variation","end":140432372,"alleles":["CGAGAAACACC","C"]},{"start":140432363,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140432363,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1408440455","clinical_significance":[]},{"start":140432367,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140432367,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130191022","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585442679","end":140432370,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140432370,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432371,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140432371,"id":"rs1171013069","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140432376,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140432376,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1465749311"},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140432378,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432378,"source":"dbSNP","seq_region_name":"7","id":"rs1799742778","clinical_significance":[]},{"source":"dbSNP","start":140432381,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140432381,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1214254111","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1585442684","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432382,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","G"],"end":140432382},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799742825","alleles":["-","A"],"end":140432382,"feature_type":"variation","strand":1,"source":"dbSNP","start":140432383,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1173009108","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432383,"source":"dbSNP","strand":1,"feature_type":"variation","end":140432383,"alleles":["C","A","G","T"]},{"end":140432383,"alleles":["C","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140432383,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799742861","seq_region_name":"7"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432384,"feature_type":"variation","strand":1,"end":140432385,"alleles":["AA","AAA","AAAA"],"clinical_significance":[],"id":"rs1373929652","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799742903","clinical_significance":[],"end":140432390,"alleles":["AATTAAA","AA"],"strand":1,"feature_type":"variation","start":140432384,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"start":140432385,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["ATTA","A"],"end":140432388,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1448111887","clinical_significance":[]},{"end":140432386,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","start":140432386,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1190483700","clinical_significance":[]},{"alleles":["TT","T"],"end":140432387,"feature_type":"variation","strand":1,"source":"dbSNP","start":140432386,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs374200782"},{"end":140432387,"alleles":["TT","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140432386,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1563078380"},{"source":"dbSNP","start":140432387,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140432386,"alleles":["-","A","AA","AAA","AAAA","AAAAA","AAAAAA","AAAAAAA","AAAAAAAA"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1563078382"},{"start":140432387,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140432387,"alleles":["T","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs28538811","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1491554605","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432387,"feature_type":"variation","strand":1,"end":140432388,"alleles":["TA","-"]},{"end":140432389,"alleles":["TAA","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140432387,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1257689547","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1198328811","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432387,"source":"dbSNP","strand":1,"feature_type":"variation","end":140432390,"alleles":["TAAA","-"]},{"seq_region_name":"7","id":"rs1343857585","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["TAAAA","-"],"end":140432391,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432387,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1251611379","clinical_significance":[],"start":140432387,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140432392,"alleles":["TAAAAA","-"],"strand":1,"feature_type":"variation"},{"id":"rs1230316874","seq_region_name":"7","clinical_significance":[],"end":140432393,"alleles":["TAAAAAA","-"],"strand":1,"feature_type":"variation","start":140432387,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"id":"rs1799743195","seq_region_name":"7","clinical_significance":[],"end":140432394,"alleles":["TAAAAAAA","-"],"strand":1,"feature_type":"variation","start":140432387,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"id":"rs1799743210","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432387,"source":"dbSNP","strand":1,"feature_type":"variation","end":140432398,"alleles":["TAAAAAAAAAAA","-"]},{"seq_region_name":"7","id":"rs1799743223","clinical_significance":[],"alleles":["-","GAAAA"],"end":140432387,"strand":1,"feature_type":"variation","start":140432388,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"end":140432388,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140432388,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1332280235","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs904318972","source":"dbSNP","start":140432388,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["AAAAAAAAAAAA","AAAA","AAAAAAAAAAA","AAAAAAAAAAAAA","AAAAAAAAAAAAAA","AAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAA"],"end":140432399,"feature_type":"variation","strand":1},{"alleles":["AAAAAAAAAAACAAAAAAAAAAACAA","AAAAAAAAAAACAA"],"end":140432414,"feature_type":"variation","strand":1,"source":"dbSNP","start":140432389,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1031623924"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1397468183","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140432390,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432390},{"source":"dbSNP","start":140432393,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140432393,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1191969154"},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140432394,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432394,"source":"dbSNP","seq_region_name":"7","id":"rs1427380385","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140432395,"alleles":["A","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432395,"clinical_significance":[],"seq_region_name":"7","id":"rs1799743416"},{"end":140432405,"alleles":["AAAAACAAAAA","AAAAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140432395,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799743432"},{"id":"rs1164723225","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140432396,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432396,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1431469579","seq_region_name":"7","end":140432396,"alleles":["A","ACA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140432396,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140432396,"alleles":["-","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432397,"clinical_significance":[],"seq_region_name":"7","id":"rs1799743494"},{"end":140432397,"alleles":["A","ACA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140432397,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799743505"},{"seq_region_name":"7","id":"rs891705854","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140432398,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432398,"source":"dbSNP"},{"start":140432399,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140432399,"alleles":["A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1369619545","clinical_significance":[]},{"start":140432399,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["ACA","A"],"end":140432401,"strand":1,"feature_type":"variation","id":"rs1175978362","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432400,"source":"dbSNP","strand":1,"feature_type":"variation","end":140432399,"alleles":["-","AC"],"seq_region_name":"7","id":"rs1799743582","clinical_significance":[]},{"source":"dbSNP","start":140432400,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140432400,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs7456866"},{"strand":1,"feature_type":"variation","end":140432400,"alleles":["C","-"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432400,"source":"dbSNP","seq_region_name":"7","id":"rs1184792581","clinical_significance":[]},{"source":"dbSNP","start":140432401,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140432401,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1170361712","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432401,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AAAAAAAAAAA","AAAAAAAAA","AAAAAAAAAA","AAAAAAAAAAAA","AAAAAAAAAAAAA","AAAAAAAAAAAAAAA"],"end":140432411,"seq_region_name":"7","id":"rs56136410","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799743749","clinical_significance":[],"strand":1,"feature_type":"variation","end":140432401,"alleles":["-","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432402,"source":"dbSNP"},{"source":"dbSNP","start":140432403,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","C","G"],"end":140432403,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1358398198"},{"id":"rs1014288637","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["-","C"],"end":140432403,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432404,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1422044186","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432404,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140432404},{"feature_type":"variation","strand":1,"alleles":["A","C","T"],"end":140432405,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432405,"clinical_significance":[],"id":"rs891519826","seq_region_name":"7"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432406,"feature_type":"variation","strand":1,"end":140432405,"alleles":["-","C"],"clinical_significance":[],"id":"rs1799743844","seq_region_name":"7"},{"alleles":["A","C"],"end":140432406,"feature_type":"variation","strand":1,"source":"dbSNP","start":140432406,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799743860"},{"end":140432407,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140432407,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1014106342","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140432408,"alleles":["A","ACA"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432408,"source":"dbSNP","seq_region_name":"7","id":"rs1336471997","clinical_significance":[]},{"end":140432408,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140432408,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1408262164","seq_region_name":"7","clinical_significance":[]},{"start":140432409,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","C"],"end":140432409,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1024299278","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799743919","clinical_significance":[],"alleles":["AAACAA","AA"],"end":140432414,"strand":1,"feature_type":"variation","start":140432409,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1024529264","source":"dbSNP","start":140432410,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140432410,"feature_type":"variation","strand":1},{"start":140432410,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140432414,"alleles":["AACAA","AA"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1563078418","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799743974","feature_type":"variation","strand":1,"end":140432411,"alleles":["A","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432411},{"alleles":["ACA","A"],"end":140432413,"strand":1,"feature_type":"variation","start":140432411,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1799743993","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs905788362","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432412,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140432412},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432415,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140432415,"id":"rs1799744045","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799744064","clinical_significance":[],"start":140432416,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140432416,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1799744085","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432418,"source":"dbSNP","strand":1,"feature_type":"variation","end":140432418,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs1163253220","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432420,"source":"dbSNP","strand":1,"feature_type":"variation","end":140432420,"alleles":["G","A"]},{"end":140432421,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140432421,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799744123","seq_region_name":"7"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432423,"feature_type":"variation","strand":1,"end":140432423,"alleles":["A","C","G"],"clinical_significance":[],"id":"rs1472159689","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs980143575","end":140432427,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140432427,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"id":"rs1799744192","seq_region_name":"7","clinical_significance":[],"end":140432428,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140432428,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432432,"feature_type":"variation","strand":1,"end":140432432,"alleles":["C","A"],"clinical_significance":[],"id":"rs1799744211","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1183831412","clinical_significance":[],"end":140432435,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140432435,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"id":"rs1799744260","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432435,"source":"dbSNP","strand":1,"feature_type":"variation","end":140432440,"alleles":["CTCTCT","CTCT"]},{"seq_region_name":"7","id":"rs1799744275","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432436,"source":"dbSNP","strand":1,"feature_type":"variation","end":140432436,"alleles":["T","A"]},{"seq_region_name":"7","id":"rs1471423034","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140432437,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432437,"source":"dbSNP"},{"end":140432439,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140432439,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1250727185","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799744331","source":"dbSNP","start":140432440,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140432443,"alleles":["TGTG","TG"],"feature_type":"variation","strand":1},{"alleles":["G","C"],"end":140432441,"feature_type":"variation","strand":1,"source":"dbSNP","start":140432441,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1453180217"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1364882143","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432445,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140432445},{"start":140432446,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140432446,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799744394","clinical_significance":[]},{"id":"rs1799744414","seq_region_name":"7","clinical_significance":[],"start":140432447,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140432447,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1799744445","seq_region_name":"7","source":"dbSNP","start":140432450,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140432450,"alleles":["C","G"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140432452,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140432452,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1287605569"},{"start":140432453,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140432453,"strand":1,"feature_type":"variation","id":"rs1209220692","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432456,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140432456,"id":"rs1799744496","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799744515","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432458,"feature_type":"variation","strand":1,"end":140432458,"alleles":["A","AA"]},{"strand":1,"feature_type":"variation","end":140432458,"alleles":["A","-"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432458,"source":"dbSNP","seq_region_name":"7","id":"rs1799744532","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432462,"source":"dbSNP","strand":1,"feature_type":"variation","end":140432462,"alleles":["G","A"],"seq_region_name":"7","id":"rs1001413368","clinical_significance":[]},{"seq_region_name":"7","id":"rs1351437554","clinical_significance":[],"strand":1,"feature_type":"variation","end":140432463,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432463,"source":"dbSNP"},{"id":"rs1799744611","seq_region_name":"7","clinical_significance":[],"end":140432464,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140432464,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1976851","end":140432466,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140432466,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140432467,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432467,"source":"dbSNP","seq_region_name":"7","id":"rs952280049","clinical_significance":[]},{"clinical_significance":[],"id":"rs1350112653","seq_region_name":"7","source":"dbSNP","start":140432471,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140432471,"alleles":["T","C"],"feature_type":"variation","strand":1},{"id":"rs1367974708","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140432472,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432472,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1284230447","clinical_significance":[],"alleles":["AGAAG","AG"],"end":140432476,"strand":1,"feature_type":"variation","start":140432472,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"alleles":["GAGAG","GAG"],"end":140432481,"feature_type":"variation","strand":1,"source":"dbSNP","start":140432477,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1730373124"},{"id":"rs963408753","seq_region_name":"7","clinical_significance":[],"start":140432480,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140432480,"strand":1,"feature_type":"variation"},{"alleles":["G","A","C"],"end":140432481,"strand":1,"feature_type":"variation","start":140432481,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs564375503","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140432484,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432484,"source":"dbSNP","seq_region_name":"7","id":"rs1585442845","clinical_significance":[]},{"end":140432486,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140432486,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799744850"},{"strand":1,"feature_type":"variation","alleles":["T","-"],"end":140432487,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432487,"source":"dbSNP","seq_region_name":"7","id":"rs1799744861","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432487,"feature_type":"variation","strand":1,"alleles":["TGGT","TGGTGGT"],"end":140432490,"clinical_significance":[],"seq_region_name":"7","id":"rs1401818456"},{"source":"dbSNP","start":140432489,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140432489,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1585442849","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1799744918","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432496,"feature_type":"variation","strand":1,"end":140432496,"alleles":["A","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1285103041","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432499,"feature_type":"variation","strand":1,"end":140432499,"alleles":["C","G"]},{"source":"dbSNP","start":140432504,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140432504,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1026424046"},{"id":"rs531651208","seq_region_name":"7","clinical_significance":[],"start":140432505,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140432505,"strand":1,"feature_type":"variation"},{"start":140432507,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","-"],"end":140432507,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799745005","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs944939161","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432508,"feature_type":"variation","strand":1,"end":140432510,"alleles":["GGG","G"]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140432511,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432511,"source":"dbSNP","seq_region_name":"7","id":"rs1799745044","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799745065","clinical_significance":[],"strand":1,"feature_type":"variation","end":140432532,"alleles":["CTTGGGCACTACGTATCCTTGG","CTTGG"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432511,"source":"dbSNP"},{"end":140432518,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140432518,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799745085"},{"end":140432522,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140432522,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs987673154"},{"seq_region_name":"7","id":"rs1410767712","clinical_significance":[],"alleles":["G","A"],"end":140432523,"strand":1,"feature_type":"variation","start":140432523,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"alleles":["A","G"],"end":140432525,"strand":1,"feature_type":"variation","start":140432525,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs912005957","clinical_significance":[]},{"alleles":["T","G"],"end":140432530,"feature_type":"variation","strand":1,"source":"dbSNP","start":140432530,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs922245558"},{"start":140432533,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140432533,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799745171","clinical_significance":[]},{"source":"dbSNP","start":140432537,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140432537,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs943544767","seq_region_name":"7"},{"source":"dbSNP","start":140432542,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140432542,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1244790331","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799745241","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432545,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140432545},{"clinical_significance":[],"seq_region_name":"7","id":"rs1198039934","feature_type":"variation","strand":1,"end":140432546,"alleles":["C","G","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432546},{"clinical_significance":[],"seq_region_name":"7","id":"rs932407691","source":"dbSNP","start":140432550,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140432550,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140432553,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432553,"source":"dbSNP","seq_region_name":"7","id":"rs974999029","clinical_significance":[]},{"start":140432555,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140432555,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs926192935","clinical_significance":[]},{"seq_region_name":"7","id":"rs549983936","clinical_significance":[],"start":140432557,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140432557,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1799745342","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432564,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140432564},{"seq_region_name":"7","id":"rs2130191470","clinical_significance":[],"alleles":["A","C"],"end":140432568,"strand":1,"feature_type":"variation","start":140432568,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799745352","source":"dbSNP","start":140432569,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140432569,"alleles":["G","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799745366","source":"dbSNP","start":140432570,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140432570,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1221201993","clinical_significance":[],"end":140432572,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140432572,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"end":140432573,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140432573,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1442142734","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140432582,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432582,"clinical_significance":[],"seq_region_name":"7","id":"rs1157333917"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140432584,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432584,"clinical_significance":[],"seq_region_name":"7","id":"rs1585442891"},{"start":140432589,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140432601,"alleles":["ATTAAACTCTTGT","-"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs557753168","clinical_significance":[]},{"alleles":["ATTAAACTCTTGT","ATTAAACTCTTGTATTAAACTCTTGT"],"end":140432601,"strand":1,"feature_type":"variation","start":140432589,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs2130191490","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432590,"feature_type":"variation","strand":1,"end":140432590,"alleles":["T","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799745483"},{"seq_region_name":"7","id":"rs1799745500","clinical_significance":[],"start":140432594,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140432594,"strand":1,"feature_type":"variation"},{"end":140432597,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140432597,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1406255170","seq_region_name":"7","clinical_significance":[]},{"end":140432598,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140432598,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585442895"},{"seq_region_name":"7","id":"rs1432022700","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432599,"source":"dbSNP","strand":1,"feature_type":"variation","end":140432599,"alleles":["T","C"]},{"feature_type":"variation","strand":1,"end":140432600,"alleles":["G","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432600,"clinical_significance":[],"id":"rs1053344568","seq_region_name":"7"},{"id":"rs1799745573","seq_region_name":"7","clinical_significance":[],"end":140432602,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140432602,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1799745594","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432610,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140432610},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799745617","alleles":["G","A"],"end":140432611,"feature_type":"variation","strand":1,"source":"dbSNP","start":140432611,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs757219251","clinical_significance":[],"alleles":["G","A"],"end":140432613,"strand":1,"feature_type":"variation","start":140432613,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"strand":1,"feature_type":"variation","end":140432617,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432617,"source":"dbSNP","id":"rs891741091","seq_region_name":"7","clinical_significance":[]},{"end":140432625,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140432625,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1052694904","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140432625,"alleles":["G","-"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432625,"source":"dbSNP","id":"rs1799745690","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799745705","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432626,"feature_type":"variation","strand":1,"end":140432626,"alleles":["T","C"]},{"id":"rs2130191542","seq_region_name":"7","clinical_significance":[],"alleles":["G","T"],"end":140432627,"strand":1,"feature_type":"variation","start":140432627,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"alleles":["A","C"],"end":140432641,"strand":1,"feature_type":"variation","start":140432641,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799745724","clinical_significance":[]},{"clinical_significance":[],"id":"rs912993841","seq_region_name":"7","end":140432650,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140432650,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799745754","feature_type":"variation","strand":1,"end":140432651,"alleles":["CC","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432650},{"source":"dbSNP","start":140432651,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140432651,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799745778"},{"clinical_significance":[],"id":"rs1347818005","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140432654,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432654},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140432655,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432655,"source":"dbSNP","seq_region_name":"7","id":"rs1435305269","clinical_significance":[]},{"seq_region_name":"7","id":"rs10085669","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140432659,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432659,"source":"dbSNP"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432660,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140432660,"clinical_significance":[],"seq_region_name":"7","id":"rs1799745914"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130191569","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432661,"feature_type":"variation","strand":1,"end":140432661,"alleles":["A","G"]},{"feature_type":"variation","strand":1,"end":140432663,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432663,"clinical_significance":[],"seq_region_name":"7","id":"rs1045571108"},{"feature_type":"variation","strand":1,"end":140432664,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432664,"clinical_significance":[],"seq_region_name":"7","id":"rs1444500681"},{"source":"dbSNP","start":140432668,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140432668,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799746017"},{"alleles":["C","G"],"end":140432670,"strand":1,"feature_type":"variation","start":140432670,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799746044","clinical_significance":[]},{"end":140432672,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140432672,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs529405706","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs10085469","seq_region_name":"7","source":"dbSNP","start":140432673,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140432673,"alleles":["G","A","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1238145787","end":140432674,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140432674,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"id":"rs1563078482","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140432675,"strand":1,"feature_type":"variation","start":140432675,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140432678,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432678,"clinical_significance":[],"seq_region_name":"7","id":"rs1799746160"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432682,"source":"dbSNP","strand":1,"feature_type":"variation","end":140432682,"alleles":["C","A"],"id":"rs1799746196","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1024330327","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432686,"feature_type":"variation","strand":1,"end":140432686,"alleles":["G","A"]},{"alleles":["A","G"],"end":140432688,"strand":1,"feature_type":"variation","start":140432688,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799746247","clinical_significance":[]},{"clinical_significance":[],"id":"rs1229758796","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140432691,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432691},{"id":"rs1310670868","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432697,"source":"dbSNP","strand":1,"feature_type":"variation","end":140432697,"alleles":["G","A"]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432701,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140432701,"id":"rs1799746303","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140432703,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432703,"clinical_significance":[],"id":"rs905829047","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1799746342","seq_region_name":"7","source":"dbSNP","start":140432704,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140432704,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140432705,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432705,"source":"dbSNP","seq_region_name":"7","id":"rs1001361084","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432706,"feature_type":"variation","strand":1,"end":140432706,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1038324459"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432708,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140432708,"seq_region_name":"7","id":"rs1799746410","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1213263358","source":"dbSNP","start":140432709,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140432709,"feature_type":"variation","strand":1},{"alleles":["G","A"],"end":140432710,"feature_type":"variation","strand":1,"source":"dbSNP","start":140432710,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs566051222"},{"start":140432712,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140432712,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585442962","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432714,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140432714,"seq_region_name":"7","id":"rs539775316","clinical_significance":[]},{"seq_region_name":"7","id":"rs1027777663","clinical_significance":[],"start":140432715,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140432715,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1302925106","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432716,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140432716},{"seq_region_name":"7","id":"rs1799746576","clinical_significance":[],"start":140432722,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140432722,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"start":140432725,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","C"],"end":140432725,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs994859579","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799746608","clinical_significance":[],"start":140432727,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140432727,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1799746630","seq_region_name":"7","source":"dbSNP","start":140432728,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140432728,"alleles":["A","G"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140432729,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432729,"source":"dbSNP","seq_region_name":"7","id":"rs1449698645","clinical_significance":[]},{"start":140432730,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140432730,"alleles":["T","A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1357062782","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432731,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140432731,"seq_region_name":"7","id":"rs1799746680","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1026707422","end":140432734,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140432734,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"alleles":["C","T"],"end":140432738,"feature_type":"variation","strand":1,"source":"dbSNP","start":140432738,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs952208175"},{"feature_type":"variation","strand":1,"end":140432739,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432739,"clinical_significance":[],"seq_region_name":"7","id":"rs983665796"},{"seq_region_name":"7","id":"rs1799746991","clinical_significance":[],"end":140432740,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140432740,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1799747004","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432744,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140432744},{"feature_type":"variation","strand":1,"end":140432747,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432747,"clinical_significance":[],"seq_region_name":"7","id":"rs1238042244"},{"start":140432750,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140432750,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs1166585367","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140432752,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432752,"source":"dbSNP","seq_region_name":"7","id":"rs1799747058","clinical_significance":[]},{"clinical_significance":[],"id":"rs1448822301","seq_region_name":"7","alleles":["C","T"],"end":140432755,"feature_type":"variation","strand":1,"source":"dbSNP","start":140432755,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"start":140432756,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140432756,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs552440488","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130191676","clinical_significance":[],"start":140432757,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","C"],"end":140432757,"strand":1,"feature_type":"variation"},{"end":140432761,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140432761,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs966335375","seq_region_name":"7","clinical_significance":[]},{"end":140432763,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140432763,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799747142","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432764,"feature_type":"variation","strand":1,"end":140432764,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1321668604"},{"id":"rs1165431474","seq_region_name":"7","clinical_significance":[],"end":140432765,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140432765,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1009433377","clinical_significance":[],"start":140432766,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140432766,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs922281626","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432767,"feature_type":"variation","strand":1,"alleles":["G","A","C","T"],"end":140432767},{"clinical_significance":[],"seq_region_name":"7","id":"rs1381698948","source":"dbSNP","start":140432768,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140432768,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs932355181","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432769,"feature_type":"variation","strand":1,"end":140432769,"alleles":["T","C"]},{"feature_type":"variation","strand":1,"alleles":["C","A","G"],"end":140432770,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432770,"clinical_significance":[],"seq_region_name":"7","id":"rs9648834"},{"end":140432777,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140432777,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1272979153","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140432782,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432782,"source":"dbSNP","seq_region_name":"7","id":"rs964875394","clinical_significance":[]},{"id":"rs1204994952","seq_region_name":"7","clinical_significance":[],"start":140432786,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140432786,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432791,"feature_type":"variation","strand":1,"end":140432791,"alleles":["C","T"],"clinical_significance":[],"id":"rs1360816158","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1404447507","source":"dbSNP","start":140432794,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140432794,"feature_type":"variation","strand":1},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432797,"feature_type":"variation","strand":1,"end":140432797,"alleles":["A","G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs925750917"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432800,"source":"dbSNP","strand":1,"feature_type":"variation","end":140432800,"alleles":["G","A"],"id":"rs1376387015","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563078527","alleles":["T","C"],"end":140432801,"feature_type":"variation","strand":1,"source":"dbSNP","start":140432801,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432804,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140432804,"clinical_significance":[],"seq_region_name":"7","id":"rs1799747577"},{"clinical_significance":[],"seq_region_name":"7","id":"rs113857454","source":"dbSNP","start":140432805,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140432805,"alleles":["G","A"],"feature_type":"variation","strand":1},{"alleles":["G","A","C"],"end":140432807,"strand":1,"feature_type":"variation","start":140432807,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1170884248","clinical_significance":[]},{"start":140432809,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140432809,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1372132443","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432813,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140432813,"clinical_significance":[],"seq_region_name":"7","id":"rs1799747704"},{"seq_region_name":"7","id":"rs1305955891","clinical_significance":[],"strand":1,"feature_type":"variation","end":140432819,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432819,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1585443046","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140432820,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432820,"source":"dbSNP"},{"id":"rs935737247","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432824,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140432824},{"alleles":["A","G"],"end":140432838,"strand":1,"feature_type":"variation","start":140432838,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1799747774","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1350383199","clinical_significance":[],"start":140432840,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","C","T"],"end":140432840,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140432844,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432844,"source":"dbSNP","seq_region_name":"7","id":"rs1799747806","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799747822","clinical_significance":[],"end":140432846,"alleles":["G","C","T"],"strand":1,"feature_type":"variation","start":140432846,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432849,"source":"dbSNP","strand":1,"feature_type":"variation","end":140432849,"alleles":["T","A"],"seq_region_name":"7","id":"rs1799747844","clinical_significance":[]},{"end":140432850,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140432850,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1799747862","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1166880523","seq_region_name":"7","source":"dbSNP","start":140432851,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140432851,"feature_type":"variation","strand":1},{"end":140432852,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140432852,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799747904"},{"alleles":["T","C"],"end":140432853,"feature_type":"variation","strand":1,"source":"dbSNP","start":140432853,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799747922","seq_region_name":"7"},{"source":"dbSNP","start":140432859,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140432859,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs539153425"},{"clinical_significance":[],"seq_region_name":"7","id":"rs974863213","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140432860,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432860},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432861,"feature_type":"variation","strand":1,"end":140432861,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs770140575"},{"id":"rs1183118297","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140432872,"strand":1,"feature_type":"variation","start":140432872,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"alleles":["G","A"],"end":140432875,"strand":1,"feature_type":"variation","start":140432875,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1473699935","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140432876,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140432876,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1585443064","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432879,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140432879,"seq_region_name":"7","id":"rs1585443067","clinical_significance":[]},{"seq_region_name":"7","id":"rs1330603549","clinical_significance":[],"end":140432882,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140432882,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140432884,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432884,"clinical_significance":[],"id":"rs957588916","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140432885,"alleles":["G","A","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432885,"clinical_significance":[],"seq_region_name":"7","id":"rs370267687"},{"alleles":["T","G"],"end":140432889,"feature_type":"variation","strand":1,"source":"dbSNP","start":140432889,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799748223"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799748242","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432891,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140432891},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432894,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140432894,"id":"rs866633923","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799748288","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432895,"feature_type":"variation","strand":1,"end":140432895,"alleles":["C","T"]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432896,"source":"dbSNP","strand":1,"feature_type":"variation","end":140432896,"alleles":["A","G"],"id":"rs1799748310","seq_region_name":"7","clinical_significance":[]},{"id":"rs1799748330","seq_region_name":"7","clinical_significance":[],"start":140432898,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140432898,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799748344","alleles":["G","A"],"end":140432899,"feature_type":"variation","strand":1,"source":"dbSNP","start":140432899,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140432901,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140432901,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1267719300"},{"start":140432907,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140432908,"alleles":["GC","-"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1220065683","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130191831","clinical_significance":[],"end":140432912,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140432912,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1585443081","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140432915,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432915,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432921,"source":"dbSNP","strand":1,"feature_type":"variation","end":140432921,"alleles":["G","A"],"seq_region_name":"7","id":"rs1282249136","clinical_significance":[]},{"seq_region_name":"7","id":"rs1319349948","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432925,"source":"dbSNP","strand":1,"feature_type":"variation","end":140432925,"alleles":["G","A"]},{"feature_type":"variation","strand":1,"end":140432926,"alleles":["A","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432926,"clinical_significance":[],"seq_region_name":"7","id":"rs1585443086"},{"clinical_significance":[],"id":"rs1799748450","seq_region_name":"7","end":140432927,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140432927,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"id":"rs977229649","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140432928,"alleles":["T","A","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432928,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140432929,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432929,"clinical_significance":[],"seq_region_name":"7","id":"rs1799748494"},{"end":140432930,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140432930,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799748511","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140432931,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432931,"clinical_significance":[],"seq_region_name":"7","id":"rs1799748527"},{"seq_region_name":"7","id":"rs891599954","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140432933,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432933,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799748569","clinical_significance":[],"alleles":["-","A"],"end":140432933,"strand":1,"feature_type":"variation","start":140432934,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432934,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140432934,"id":"rs1327048239","seq_region_name":"7","clinical_significance":[]},{"start":140432935,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["-","A","AA","AAA","AAAA"],"end":140432934,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799748616","clinical_significance":[]},{"end":140432935,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140432935,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1231296027"},{"start":140432935,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140432935,"alleles":["C","-"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799748668","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs34301337","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432936,"feature_type":"variation","strand":1,"end":140432950,"alleles":["AAAAAAAAAAAAAAA","AAAAAAAAAAA","AAAAAAAAAAAA","AAAAAAAAAAAAA","AAAAAAAAAAAAAA","AAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA"]},{"feature_type":"variation","strand":1,"end":140432944,"alleles":["A","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432944,"clinical_significance":[],"id":"rs1410031211","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1799748858","seq_region_name":"7","end":140432946,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140432946,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140432947,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140432947,"alleles":["A","AGA"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs949956425"},{"source":"dbSNP","start":140432947,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140432947,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799748876"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432947,"source":"dbSNP","strand":1,"feature_type":"variation","end":140432948,"alleles":["AA","AAGAA"],"seq_region_name":"7","id":"rs1554443798","clinical_significance":[]},{"end":140432949,"alleles":["AAA","AAAGAAA"],"strand":1,"feature_type":"variation","start":140432947,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1554443799","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1189941837","end":140432960,"alleles":["AAAAGAAAAGAAAA","AAAAGAAAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140432947,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1258886981","source":"dbSNP","start":140432948,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140432948,"feature_type":"variation","strand":1},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432948,"feature_type":"variation","strand":1,"end":140432954,"alleles":["AAAGAAA","AAA","AAAGAAAGAAA"],"clinical_significance":[],"seq_region_name":"7","id":"rs1251769653"},{"seq_region_name":"7","id":"rs1799749027","clinical_significance":[],"start":140432949,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["AA","AAAGAA"],"end":140432950,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140432950,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432950,"source":"dbSNP","seq_region_name":"7","id":"rs1799749048","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799749067","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["AGA","A"],"end":140432952,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432950,"source":"dbSNP"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432951,"feature_type":"variation","strand":1,"end":140432951,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs372200502"},{"clinical_significance":[],"id":"rs1799749122","seq_region_name":"7","feature_type":"variation","strand":1,"end":140432951,"alleles":["G","-"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432951},{"source":"dbSNP","start":140432953,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140432953,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1330683015"},{"source":"dbSNP","start":140432954,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140432958,"alleles":["AAGAA","AA"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799749165"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140432956,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432956,"source":"dbSNP","id":"rs1196893695","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1265825550","end":140432957,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140432957,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"alleles":["A","C"],"end":140432958,"feature_type":"variation","strand":1,"source":"dbSNP","start":140432958,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799749224"},{"seq_region_name":"7","id":"rs1799749242","clinical_significance":[],"strand":1,"feature_type":"variation","end":140432960,"alleles":["AA","AAGACAA"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432959,"source":"dbSNP"},{"end":140432960,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140432960,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799749256","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1443542125","feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140432961,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432961},{"seq_region_name":"7","id":"rs949745479","clinical_significance":[],"strand":1,"feature_type":"variation","end":140432962,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432962,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799749319","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432964,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140432964},{"clinical_significance":[],"seq_region_name":"7","id":"rs1475061498","end":140432965,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140432965,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140432969,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140432969,"source":"dbSNP","seq_region_name":"7","id":"rs1045924387","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140432974,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432974,"clinical_significance":[],"seq_region_name":"7","id":"rs1384952361"},{"seq_region_name":"7","id":"rs1313730808","clinical_significance":[],"start":140432978,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140432978,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140432979,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432979,"clinical_significance":[],"seq_region_name":"7","id":"rs1193941502"},{"clinical_significance":[],"id":"rs1799749456","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432983,"feature_type":"variation","strand":1,"end":140432983,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799749474","source":"dbSNP","start":140432984,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140432984,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140432985,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432985,"clinical_significance":[],"seq_region_name":"7","id":"rs1321220458"},{"alleles":["GAATCATG","GAATCATGAATCATG"],"end":140432994,"strand":1,"feature_type":"variation","start":140432987,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1437333468","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799749522","seq_region_name":"7","source":"dbSNP","start":140432990,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["TCATGGTCATG","TCATGGTCATGGTCATG"],"end":140433000,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs905774846","clinical_significance":[],"alleles":["A","G"],"end":140432992,"strand":1,"feature_type":"variation","start":140432992,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"start":140432993,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140432993,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1158638943","clinical_significance":[]},{"clinical_significance":[],"id":"rs2130191991","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140432994,"feature_type":"variation","strand":1,"end":140432994,"alleles":["G","T"]},{"seq_region_name":"7","id":"rs1799749587","clinical_significance":[],"end":140432995,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140432995,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"alleles":["C","T"],"end":140432997,"strand":1,"feature_type":"variation","start":140432997,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1466769565","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799749630","feature_type":"variation","strand":1,"end":140433000,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433000},{"alleles":["C","A","T"],"end":140433013,"feature_type":"variation","strand":1,"source":"dbSNP","start":140433013,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1379664733","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1001558406","feature_type":"variation","strand":1,"end":140433014,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433014},{"id":"rs1049517345","seq_region_name":"7","clinical_significance":[],"start":140433024,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","G"],"end":140433024,"strand":1,"feature_type":"variation"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433029,"feature_type":"variation","strand":1,"end":140433029,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585443146"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1191107882","end":140433031,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140433031,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433031,"feature_type":"variation","strand":1,"end":140433032,"alleles":["CA","-"],"clinical_significance":[],"seq_region_name":"7","id":"rs1391320152"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799749762","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433033,"feature_type":"variation","strand":1,"end":140433033,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1799749776","clinical_significance":[],"start":140433042,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140433042,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs927052369","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433044,"source":"dbSNP","strand":1,"feature_type":"variation","end":140433044,"alleles":["C","T"]},{"strand":1,"feature_type":"variation","end":140433048,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433048,"source":"dbSNP","seq_region_name":"7","id":"rs1465823179","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1245702492","source":"dbSNP","start":140433049,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140433049,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799749830","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433052,"feature_type":"variation","strand":1,"alleles":["G","C","T"],"end":140433052},{"id":"rs937183381","seq_region_name":"7","clinical_significance":[],"alleles":["G","A","T"],"end":140433053,"strand":1,"feature_type":"variation","start":140433053,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"alleles":["A","G"],"end":140433055,"strand":1,"feature_type":"variation","start":140433055,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1799749882","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585443158","end":140433063,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140433063,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1563078579","clinical_significance":[],"start":140433064,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140433064,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799749933","alleles":["G","C"],"end":140433074,"feature_type":"variation","strand":1,"source":"dbSNP","start":140433074,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1585443162","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433076,"source":"dbSNP","strand":1,"feature_type":"variation","end":140433076,"alleles":["G","A"]},{"clinical_significance":[],"id":"rs1799749979","seq_region_name":"7","source":"dbSNP","start":140433078,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140433078,"alleles":["A","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1257456057","clinical_significance":[],"alleles":["G","C"],"end":140433079,"strand":1,"feature_type":"variation","start":140433079,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799750016","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433086,"feature_type":"variation","strand":1,"end":140433088,"alleles":["AAA","AA"]},{"clinical_significance":[],"id":"rs9648835","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A","C","T"],"end":140433091,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433091},{"start":140433092,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140433092,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799750128","clinical_significance":[]},{"seq_region_name":"7","id":"rs1015093183","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433094,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140433094},{"strand":1,"feature_type":"variation","end":140433096,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433096,"source":"dbSNP","seq_region_name":"7","id":"rs2130192073","clinical_significance":[]},{"source":"dbSNP","start":140433101,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140433101,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1230545093"},{"clinical_significance":[],"id":"rs75398337","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433103,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140433103},{"seq_region_name":"7","id":"rs997633777","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140433105,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433105,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799750247","source":"dbSNP","start":140433107,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140433107,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1396760657","feature_type":"variation","strand":1,"end":140433109,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433109},{"alleles":["T","C"],"end":140433111,"strand":1,"feature_type":"variation","start":140433111,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1799750282","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","G"],"end":140433112,"strand":1,"feature_type":"variation","start":140433112,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs2130192093","clinical_significance":[]},{"seq_region_name":"7","id":"rs1029241291","clinical_significance":[],"start":140433113,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140433113,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1301381861","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433115,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140433115},{"seq_region_name":"7","id":"rs1332070293","clinical_significance":[],"strand":1,"feature_type":"variation","end":140433125,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433125,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799750350","clinical_significance":[],"alleles":["A","C"],"end":140433126,"strand":1,"feature_type":"variation","start":140433126,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433135,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140433135,"clinical_significance":[],"seq_region_name":"7","id":"rs1799750374"},{"seq_region_name":"7","id":"rs1799750393","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140433136,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433136,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140433145,"alleles":["CTCTACTC","CTC"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433138,"clinical_significance":[],"id":"rs953613764","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799750442","clinical_significance":[],"end":140433140,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140433140,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"source":"dbSNP","start":140433142,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140433142,"alleles":["A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs748406414"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1391193095","source":"dbSNP","start":140433143,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140433143,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1400324045","feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140433144,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433144},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799750513","source":"dbSNP","start":140433147,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140433147,"alleles":["A","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585443195","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140433149,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433149},{"end":140433151,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140433151,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs2130192129","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140433158,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140433158,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799750543","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433163,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140433163,"seq_region_name":"7","id":"rs1279844039","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799750583","clinical_significance":[],"end":140433163,"alleles":["A","-"],"strand":1,"feature_type":"variation","start":140433163,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"alleles":["C","A","G"],"end":140433164,"feature_type":"variation","strand":1,"source":"dbSNP","start":140433164,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1342687642"},{"clinical_significance":[],"seq_region_name":"7","id":"rs994053395","source":"dbSNP","start":140433166,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140433166,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799750639","source":"dbSNP","start":140433169,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140433169,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1046970501","end":140433170,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140433170,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1216999075","seq_region_name":"7","source":"dbSNP","start":140433171,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140433171,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1269726948","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140433176,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433176},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140433179,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433179,"source":"dbSNP","id":"rs985172841","seq_region_name":"7","clinical_significance":[]},{"end":140433180,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140433180,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1799750742","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799750762","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140433183,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433183,"source":"dbSNP"},{"end":140433186,"alleles":["C","A","G"],"strand":1,"feature_type":"variation","start":140433186,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1191831385","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799750792","clinical_significance":[],"strand":1,"feature_type":"variation","end":140433188,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433188,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433191,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140433191,"seq_region_name":"7","id":"rs1799750809","clinical_significance":[]},{"end":140433193,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140433193,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799750826","clinical_significance":[]},{"seq_region_name":"7","id":"rs1345747202","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140433195,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433195,"source":"dbSNP"},{"alleles":["A","AA"],"end":140433198,"feature_type":"variation","strand":1,"source":"dbSNP","start":140433198,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799750867"},{"start":140433199,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140433199,"alleles":["C","G"],"strand":1,"feature_type":"variation","id":"rs1423959357","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433203,"feature_type":"variation","strand":1,"end":140433203,"alleles":["A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130192172"},{"seq_region_name":"7","id":"rs1202735367","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433217,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140433217},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433217,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AT","-"],"end":140433218,"seq_region_name":"7","id":"rs1257800520","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799750930","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433218,"feature_type":"variation","strand":1,"end":140433218,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799750947","feature_type":"variation","strand":1,"end":140433219,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433219},{"seq_region_name":"7","id":"rs925581759","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433221,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140433221},{"clinical_significance":[],"seq_region_name":"7","id":"rs187800343","source":"dbSNP","start":140433225,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140433225,"feature_type":"variation","strand":1},{"alleles":["C","A"],"end":140433226,"feature_type":"variation","strand":1,"source":"dbSNP","start":140433226,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs957162973"},{"alleles":["C","T"],"end":140433232,"strand":1,"feature_type":"variation","start":140433232,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1799751204","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1339987639","clinical_significance":[],"alleles":["C","T"],"end":140433237,"strand":1,"feature_type":"variation","start":140433237,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs767315990","source":"dbSNP","start":140433240,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140433240,"alleles":["G","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1485557043","clinical_significance":[],"end":140433244,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140433244,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs886471178","source":"dbSNP","start":140433245,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140433245,"alleles":["G","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1008884820","clinical_significance":[],"start":140433247,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140433247,"strand":1,"feature_type":"variation"},{"start":140433249,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140433249,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799751333","clinical_significance":[]},{"alleles":["G","A"],"end":140433254,"strand":1,"feature_type":"variation","start":140433254,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs2130192212","seq_region_name":"7","clinical_significance":[]},{"start":140433255,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140433255,"strand":1,"feature_type":"variation","id":"rs1799751351","seq_region_name":"7","clinical_significance":[]},{"start":140433260,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140433260,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799751366","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1265783393","source":"dbSNP","start":140433262,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140433262,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140433263,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140433263,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799751410"},{"source":"dbSNP","start":140433264,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140433264,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1476657156"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130192241","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140433273,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433273},{"start":140433277,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140433277,"alleles":["G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585443244","clinical_significance":[]},{"id":"rs1799751474","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433278,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140433278},{"start":140433278,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140433283,"alleles":["CAAACA","CAAACAAACA"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799751497","clinical_significance":[]},{"seq_region_name":"7","id":"rs1019469982","clinical_significance":[],"start":140433279,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140433279,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs377151190","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433286,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140433286},{"strand":1,"feature_type":"variation","end":140433293,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433293,"source":"dbSNP","seq_region_name":"7","id":"rs752659653","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585443257","clinical_significance":[],"strand":1,"feature_type":"variation","end":140433300,"alleles":["A","C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433300,"source":"dbSNP"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433306,"feature_type":"variation","strand":1,"end":140433306,"alleles":["C","T"],"clinical_significance":[],"id":"rs193008140","seq_region_name":"7"},{"seq_region_name":"7","id":"rs371921697","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433307,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140433307},{"alleles":["A","G","T"],"end":140433314,"strand":1,"feature_type":"variation","start":140433314,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799751638","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433315,"feature_type":"variation","strand":1,"end":140433315,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799751663"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140433316,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433316,"clinical_significance":[],"seq_region_name":"7","id":"rs1428289078"},{"start":140433319,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140433319,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs927222403","clinical_significance":[]},{"seq_region_name":"7","id":"rs937211257","clinical_significance":[],"strand":1,"feature_type":"variation","end":140433320,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433320,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140433323,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433323,"source":"dbSNP","seq_region_name":"7","id":"rs572066821","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs545746977","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433328,"feature_type":"variation","strand":1,"alleles":["G","C","T"],"end":140433328},{"start":140433329,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","G"],"end":140433329,"strand":1,"feature_type":"variation","id":"rs959976899","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140433330,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433330,"source":"dbSNP","seq_region_name":"7","id":"rs1585443279","clinical_significance":[]},{"clinical_significance":[],"id":"rs1033106268","seq_region_name":"7","end":140433339,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140433339,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1184905064","source":"dbSNP","start":140433342,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140433342,"feature_type":"variation","strand":1},{"alleles":["C","T"],"end":140433344,"feature_type":"variation","strand":1,"source":"dbSNP","start":140433344,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130192282"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799751890","source":"dbSNP","start":140433348,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140433348,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799751910","feature_type":"variation","strand":1,"end":140433352,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433352},{"seq_region_name":"7","id":"rs1474677447","clinical_significance":[],"strand":1,"feature_type":"variation","end":140433355,"alleles":["A","C","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433355,"source":"dbSNP"},{"id":"rs1799751948","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433359,"source":"dbSNP","strand":1,"feature_type":"variation","end":140433359,"alleles":["T","A"]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140433365,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433365,"source":"dbSNP","seq_region_name":"7","id":"rs1252198089","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433366,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140433366,"seq_region_name":"7","id":"rs957620139","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799752002","alleles":["G","A"],"end":140433368,"feature_type":"variation","strand":1,"source":"dbSNP","start":140433368,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"start":140433370,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140433370,"alleles":["G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs989507491","clinical_significance":[]},{"seq_region_name":"7","id":"rs1170762360","clinical_significance":[],"alleles":["G","A"],"end":140433383,"strand":1,"feature_type":"variation","start":140433383,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"id":"rs887733617","seq_region_name":"7","alleles":["G","A"],"end":140433385,"feature_type":"variation","strand":1,"source":"dbSNP","start":140433385,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"start":140433386,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140433386,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799752076","clinical_significance":[]},{"clinical_significance":[],"id":"rs1272165979","seq_region_name":"7","source":"dbSNP","start":140433387,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140433387,"alleles":["T","C"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140433389,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433389,"clinical_significance":[],"id":"rs913477090","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1799752128","seq_region_name":"7","source":"dbSNP","start":140433390,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140433390,"feature_type":"variation","strand":1},{"start":140433392,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140433392,"alleles":["T","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799752149","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799752171","source":"dbSNP","start":140433394,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140433394,"alleles":["T","A"],"feature_type":"variation","strand":1},{"alleles":["T","C"],"end":140433396,"feature_type":"variation","strand":1,"source":"dbSNP","start":140433396,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs971500597"},{"id":"rs1799752204","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433398,"source":"dbSNP","strand":1,"feature_type":"variation","end":140433398,"alleles":["C","T"]},{"source":"dbSNP","start":140433399,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140433399,"alleles":["A","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs981113083","seq_region_name":"7"},{"id":"rs1799752238","seq_region_name":"7","clinical_significance":[],"alleles":["AAAGACGGTTTGCAAAA","AA"],"end":140433417,"strand":1,"feature_type":"variation","start":140433401,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"alleles":["A","G"],"end":140433405,"feature_type":"variation","strand":1,"source":"dbSNP","start":140433405,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1358510888"},{"start":140433406,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140433406,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs991388618","clinical_significance":[]},{"id":"rs927049017","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433407,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140433407},{"clinical_significance":[],"seq_region_name":"7","id":"rs1004979204","feature_type":"variation","strand":1,"end":140433412,"alleles":["G","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433412},{"end":140433413,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140433413,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130192344"},{"end":140433414,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140433414,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799752356"},{"end":140433417,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140433417,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs915618697"},{"id":"rs1408357761","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433418,"source":"dbSNP","strand":1,"feature_type":"variation","end":140433420,"alleles":["CCC","CC"]},{"start":140433419,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","A","G","T"],"end":140433419,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1335598816","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140433420,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433420,"source":"dbSNP","seq_region_name":"7","id":"rs1799752423","clinical_significance":[]},{"end":140433422,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140433422,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs941684965"},{"clinical_significance":[],"seq_region_name":"7","id":"rs367729171","end":140433424,"alleles":["CC","C","CCC"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140433423,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140433427,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140433428,"alleles":["CC","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1407601222"},{"clinical_significance":[],"seq_region_name":"7","id":"rs937047644","end":140433432,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140433432,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1799752510","seq_region_name":"7","source":"dbSNP","start":140433433,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140433433,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1799752528","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433435,"source":"dbSNP","strand":1,"feature_type":"variation","end":140433435,"alleles":["C","G","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1162184754","alleles":["C","G"],"end":140433436,"feature_type":"variation","strand":1,"source":"dbSNP","start":140433436,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433448,"feature_type":"variation","strand":1,"end":140433448,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585443339"},{"source":"dbSNP","start":140433451,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140433451,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799752584"},{"id":"rs1799752606","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140433454,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433454,"source":"dbSNP"},{"id":"rs973913101","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433457,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","G"],"end":140433457},{"seq_region_name":"7","id":"rs1799752663","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140433459,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433459,"source":"dbSNP"},{"start":140433460,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140433460,"alleles":["G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799752688","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433462,"source":"dbSNP","strand":1,"feature_type":"variation","end":140433462,"alleles":["A","G"],"seq_region_name":"7","id":"rs1799752708","clinical_significance":[]},{"id":"rs901934941","seq_region_name":"7","clinical_significance":[],"alleles":["C","A","G"],"end":140433467,"strand":1,"feature_type":"variation","start":140433467,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs997664730","source":"dbSNP","start":140433468,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140433468,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1160975551","seq_region_name":"7","alleles":["TTTTT","TTTTTT"],"end":140433473,"feature_type":"variation","strand":1,"source":"dbSNP","start":140433469,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"id":"rs760589586","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140433471,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433471,"source":"dbSNP"},{"id":"rs1799752810","seq_region_name":"7","clinical_significance":[],"start":140433473,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140433473,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140433475,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140433475,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1398411754"},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140433477,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433477,"source":"dbSNP","id":"rs2130192411","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140433478,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433478,"clinical_significance":[],"seq_region_name":"7","id":"rs1232121715"},{"source":"dbSNP","start":140433484,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A","C","T"],"end":140433484,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1199403980"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1029105343","alleles":["T","G"],"end":140433486,"feature_type":"variation","strand":1,"source":"dbSNP","start":140433486,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140433493,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140433493,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1265255637"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433494,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140433494,"seq_region_name":"7","id":"rs1799752913","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433496,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140433496,"clinical_significance":[],"seq_region_name":"7","id":"rs2130192424"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140433506,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433506,"clinical_significance":[],"id":"rs763873050","seq_region_name":"7"},{"end":140433507,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140433507,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs370850693","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140433509,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140433509,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1270229759"},{"seq_region_name":"7","id":"rs1799752994","clinical_significance":[],"strand":1,"feature_type":"variation","end":140433517,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433517,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433519,"source":"dbSNP","strand":1,"feature_type":"variation","end":140433519,"alleles":["A","C","G"],"id":"rs1331758917","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799753044","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433522,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140433522},{"start":140433528,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140433528,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs1277449063","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433534,"feature_type":"variation","strand":1,"end":140433534,"alleles":["G","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1226825219"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433537,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140433537,"seq_region_name":"7","id":"rs1275812078","clinical_significance":[]},{"clinical_significance":[],"id":"rs1439150097","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433544,"feature_type":"variation","strand":1,"end":140433544,"alleles":["C","G"]},{"alleles":["T","C"],"end":140433548,"feature_type":"variation","strand":1,"source":"dbSNP","start":140433548,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799753119"},{"seq_region_name":"7","id":"rs1001502253","clinical_significance":[],"start":140433554,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140433554,"strand":1,"feature_type":"variation"},{"alleles":["G","C"],"end":140433556,"strand":1,"feature_type":"variation","start":140433556,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1032681477","clinical_significance":[]},{"start":140433557,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","C"],"end":140433557,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1439476718","clinical_significance":[]},{"seq_region_name":"7","id":"rs185132378","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433564,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140433564},{"id":"rs1799753233","seq_region_name":"7","clinical_significance":[],"start":140433565,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","T"],"end":140433565,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs772364146","clinical_significance":[],"start":140433572,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140433572,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"alleles":["G","C"],"end":140433580,"strand":1,"feature_type":"variation","start":140433580,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1799753275","seq_region_name":"7","clinical_significance":[]},{"start":140433583,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140433583,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1563078652","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799753309","alleles":["A","G"],"end":140433584,"feature_type":"variation","strand":1,"source":"dbSNP","start":140433584,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1799753326","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433585,"source":"dbSNP","strand":1,"feature_type":"variation","end":140433586,"alleles":["GG","G"]},{"feature_type":"variation","strand":1,"end":140433595,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433595,"clinical_significance":[],"seq_region_name":"7","id":"rs891025424"},{"seq_region_name":"7","id":"rs1799753370","clinical_significance":[],"start":140433598,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","G"],"end":140433598,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1273138834","feature_type":"variation","strand":1,"end":140433601,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433601},{"clinical_significance":[],"seq_region_name":"7","id":"rs753635884","alleles":["G","A","C"],"end":140433609,"feature_type":"variation","strand":1,"source":"dbSNP","start":140433609,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"alleles":["A","G"],"end":140433611,"strand":1,"feature_type":"variation","start":140433611,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1799753631","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1478926570","source":"dbSNP","start":140433614,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140433614,"alleles":["T","A","C"],"feature_type":"variation","strand":1},{"end":140433617,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140433617,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799753663"},{"id":"rs988491483","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140433618,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433618,"source":"dbSNP"},{"source":"dbSNP","start":140433620,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140433620,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1192987904"},{"clinical_significance":[],"id":"rs1347871980","seq_region_name":"7","source":"dbSNP","start":140433621,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140433621,"alleles":["G","A"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140433625,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433625,"clinical_significance":[],"seq_region_name":"7","id":"rs2130192518"},{"alleles":["G","A"],"end":140433630,"strand":1,"feature_type":"variation","start":140433630,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1250019986","clinical_significance":[]},{"id":"rs1040345948","seq_region_name":"7","clinical_significance":[],"end":140433631,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140433631,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1206984533","end":140433634,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140433634,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140433635,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433635,"source":"dbSNP","seq_region_name":"7","id":"rs1446647773","clinical_significance":[]},{"seq_region_name":"7","id":"rs1279673647","clinical_significance":[],"end":140433643,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140433643,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"alleles":["C","T"],"end":140433645,"feature_type":"variation","strand":1,"source":"dbSNP","start":140433645,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs756850131"},{"start":140433649,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140433649,"alleles":["T","C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799753837","clinical_significance":[]},{"seq_region_name":"7","id":"rs1221289024","clinical_significance":[],"end":140433650,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140433650,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433651,"source":"dbSNP","strand":1,"feature_type":"variation","end":140433651,"alleles":["A","G"],"seq_region_name":"7","id":"rs913008340","clinical_significance":[]},{"end":140433652,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140433652,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs543789302","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433656,"source":"dbSNP","strand":1,"feature_type":"variation","end":140433656,"alleles":["G","A"],"seq_region_name":"7","id":"rs2130192557","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs900602097","feature_type":"variation","strand":1,"end":140433659,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433659},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140433661,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433661,"clinical_significance":[],"seq_region_name":"7","id":"rs1303286009"},{"seq_region_name":"7","id":"rs1229817623","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433665,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140433665},{"clinical_significance":[],"id":"rs1799753997","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433666,"feature_type":"variation","strand":1,"end":140433666,"alleles":["G","T"]},{"id":"rs1365202301","seq_region_name":"7","clinical_significance":[],"start":140433667,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140433667,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140433670,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433670,"clinical_significance":[],"seq_region_name":"7","id":"rs2130192577"},{"alleles":["C","T"],"end":140433671,"strand":1,"feature_type":"variation","start":140433671,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs971122568","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1428111056","source":"dbSNP","start":140433673,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","A","G","T"],"end":140433673,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140433674,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433674,"source":"dbSNP","id":"rs1288659973","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs996177610","feature_type":"variation","strand":1,"end":140433675,"alleles":["G","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433675},{"id":"rs1799754108","seq_region_name":"7","clinical_significance":[],"start":140433679,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140433679,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"end":140433681,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140433681,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1373414990"},{"start":140433685,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140433685,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1172887257","clinical_significance":[]},{"source":"dbSNP","start":140433689,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140433689,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799754167"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433691,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140433691,"seq_region_name":"7","id":"rs1450014751","clinical_significance":[]},{"seq_region_name":"7","id":"rs1392042572","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140433697,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433697,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1184846166","alleles":["C","A","G"],"end":140433698,"feature_type":"variation","strand":1,"source":"dbSNP","start":140433698,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1799754251","clinical_significance":[],"strand":1,"feature_type":"variation","end":140433705,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433705,"source":"dbSNP"},{"start":140433709,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140433709,"alleles":["C","A"],"strand":1,"feature_type":"variation","id":"rs1799754275","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs778562679","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433716,"source":"dbSNP","strand":1,"feature_type":"variation","end":140433716,"alleles":["G","A","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1212574095","source":"dbSNP","start":140433723,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140433723,"alleles":["T","C"],"feature_type":"variation","strand":1},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433725,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140433725,"clinical_significance":[],"id":"rs1585443443","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799754960","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140433726,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433726},{"source":"dbSNP","start":140433729,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140433729,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799754977"},{"start":140433730,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140433730,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs1799754998","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140433737,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433737,"clinical_significance":[],"seq_region_name":"7","id":"rs1799755013"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1204192419","end":140433738,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140433738,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["CTTCCTTCCTT","CTTCCTT"],"end":140433748,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433738,"clinical_significance":[],"seq_region_name":"7","id":"rs927086835"},{"id":"rs1799755063","seq_region_name":"7","clinical_significance":[],"start":140433739,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["TT","T"],"end":140433740,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799755073","source":"dbSNP","start":140433742,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140433742,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433744,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140433744,"seq_region_name":"7","id":"rs1206424009","clinical_significance":[]},{"end":140433745,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140433745,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs937275327"},{"id":"rs1212264026","seq_region_name":"7","clinical_significance":[],"end":140433761,"alleles":["CTTTCTTTCTTTCTTT","CTTTCTTTCTTT","CTTTCTTTCTTTCTTTCTTT"],"strand":1,"feature_type":"variation","start":140433746,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"id":"rs1799755165","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140433748,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433748,"source":"dbSNP"},{"seq_region_name":"7","id":"rs561857391","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140433749,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433749,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs7808166","source":"dbSNP","start":140433757,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C","G"],"end":140433757,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1563078679","seq_region_name":"7","feature_type":"variation","strand":1,"end":140433758,"alleles":["C","CC"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433758},{"start":140433758,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140433758,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799755287","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140433759,"alleles":["T","A","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433759,"clinical_significance":[],"seq_region_name":"7","id":"rs187489275"},{"source":"dbSNP","start":140433759,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140433765,"alleles":["TTTTTTT","TTTTTT","TTTTTTTT"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1563078680"},{"alleles":["T","C","G"],"end":140433761,"strand":1,"feature_type":"variation","start":140433761,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799755376","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140433769,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433769,"clinical_significance":[],"seq_region_name":"7","id":"rs1312070245"},{"source":"dbSNP","start":140433771,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140433771,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1452966162"},{"end":140433772,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140433772,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1430236268","clinical_significance":[]},{"seq_region_name":"7","id":"rs547278543","clinical_significance":[],"strand":1,"feature_type":"variation","end":140433773,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433773,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799755465","source":"dbSNP","start":140433777,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140433777,"feature_type":"variation","strand":1},{"id":"rs1799755484","seq_region_name":"7","clinical_significance":[],"start":140433777,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["CTCACTC","CTC"],"end":140433783,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799755505","end":140433779,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140433779,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140433783,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140433783,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs940729778"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433786,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140433786,"clinical_significance":[],"seq_region_name":"7","id":"rs1168289305"},{"seq_region_name":"7","id":"rs1799755561","clinical_significance":[],"strand":1,"feature_type":"variation","end":140433793,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433793,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1196215931","clinical_significance":[],"start":140433795,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140433795,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1799755594","clinical_significance":[],"end":140433796,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140433796,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433801,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140433801,"seq_region_name":"7","id":"rs1409430423","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433808,"feature_type":"variation","strand":1,"end":140433808,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1020980905"},{"seq_region_name":"7","id":"rs757896419","clinical_significance":[],"alleles":["A","G","T"],"end":140433813,"strand":1,"feature_type":"variation","start":140433813,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"id":"rs779476027","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140433817,"strand":1,"feature_type":"variation","start":140433817,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799755727","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140433826,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433826},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433829,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140433829,"clinical_significance":[],"id":"rs1474356790","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140433830,"alleles":["C","A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433830,"clinical_significance":[],"seq_region_name":"7","id":"rs1160335911"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140433833,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433833,"clinical_significance":[],"seq_region_name":"7","id":"rs1183343310"},{"alleles":["C","G"],"end":140433836,"strand":1,"feature_type":"variation","start":140433836,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs981529679","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140433841,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433841,"clinical_significance":[],"seq_region_name":"7","id":"rs1799755800"},{"alleles":["C","T"],"end":140433845,"feature_type":"variation","strand":1,"source":"dbSNP","start":140433845,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799755825"},{"alleles":["T","C"],"end":140433851,"strand":1,"feature_type":"variation","start":140433851,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1799755850","seq_region_name":"7","clinical_significance":[]},{"end":140433853,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140433853,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799755874"},{"seq_region_name":"7","id":"rs1378284459","clinical_significance":[],"start":140433854,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140433854,"strand":1,"feature_type":"variation"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433855,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140433855,"clinical_significance":[],"seq_region_name":"7","id":"rs1799755908"},{"seq_region_name":"7","id":"rs1799755928","clinical_significance":[],"end":140433858,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140433858,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"id":"rs1452697281","seq_region_name":"7","source":"dbSNP","start":140433861,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140433861,"feature_type":"variation","strand":1},{"alleles":["G","A"],"end":140433867,"strand":1,"feature_type":"variation","start":140433867,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1799755972","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799756007","feature_type":"variation","strand":1,"end":140433872,"alleles":["CCCCC","CCCC"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433868},{"end":140433869,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140433869,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799756028","clinical_significance":[]},{"start":140433874,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140433874,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799756045","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799756071","end":140433875,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140433875,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"end":140433877,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140433877,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1158225172"},{"seq_region_name":"7","id":"rs1204464397","clinical_significance":[],"strand":1,"feature_type":"variation","end":140433880,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433880,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1306369664","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140433883,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433883},{"alleles":["C","G"],"end":140433884,"strand":1,"feature_type":"variation","start":140433884,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1033984327","seq_region_name":"7","clinical_significance":[]},{"id":"rs1799756175","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433885,"source":"dbSNP","strand":1,"feature_type":"variation","end":140433885,"alleles":["T","C"]},{"source":"dbSNP","start":140433887,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140433887,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799756189"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433890,"source":"dbSNP","strand":1,"feature_type":"variation","end":140433890,"alleles":["C","G"],"seq_region_name":"7","id":"rs958449337","clinical_significance":[]},{"end":140433893,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140433893,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs566137982"},{"start":140433897,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","A"],"end":140433897,"strand":1,"feature_type":"variation","id":"rs1229623914","seq_region_name":"7","clinical_significance":[]},{"start":140433902,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","C"],"end":140433902,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799756264","clinical_significance":[]},{"source":"dbSNP","start":140433903,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140433903,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799756285"},{"start":140433906,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140433906,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs933379645","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs973851009","source":"dbSNP","start":140433908,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G","T"],"end":140433908,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1050573159","seq_region_name":"7","end":140433913,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140433913,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1767877056","clinical_significance":[],"end":140433914,"alleles":["G","C","T"],"strand":1,"feature_type":"variation","start":140433914,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433915,"source":"dbSNP","strand":1,"feature_type":"variation","end":140433915,"alleles":["G","C"],"id":"rs1799756365","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140433916,"alleles":["C","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433916,"clinical_significance":[],"seq_region_name":"7","id":"rs1391798390"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1352155952","end":140433918,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140433918,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"id":"rs1296332176","seq_region_name":"7","clinical_significance":[],"alleles":["T","G"],"end":140433920,"strand":1,"feature_type":"variation","start":140433920,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"strand":1,"feature_type":"variation","alleles":["G","-"],"end":140433925,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433925,"source":"dbSNP","seq_region_name":"7","id":"rs1799756451","clinical_significance":[]},{"id":"rs1441430599","seq_region_name":"7","clinical_significance":[],"end":140433926,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140433926,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"start":140433930,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140433930,"alleles":["G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs7786260","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs551736092","feature_type":"variation","strand":1,"alleles":["A","C","T"],"end":140433938,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433938},{"alleles":["GGGG","GGG"],"end":140433945,"strand":1,"feature_type":"variation","start":140433942,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1460002637","seq_region_name":"7","clinical_significance":[]},{"end":140433948,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140433948,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs929820702","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130192845","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433955,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140433955},{"end":140433957,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140433957,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799756671","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585443551","source":"dbSNP","start":140433958,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140433958,"feature_type":"variation","strand":1},{"end":140433959,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140433959,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs576376275","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs912481836","alleles":["G","A"],"end":140433960,"feature_type":"variation","strand":1,"source":"dbSNP","start":140433960,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140433962,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433962,"clinical_significance":[],"seq_region_name":"7","id":"rs1799756742"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799756770","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433963,"feature_type":"variation","strand":1,"end":140433963,"alleles":["G","A"]},{"end":140433965,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140433965,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs192417834","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433967,"feature_type":"variation","strand":1,"end":140433967,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs543698476"},{"seq_region_name":"7","id":"rs1177064927","clinical_significance":[],"end":140433971,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140433971,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs900549927","feature_type":"variation","strand":1,"end":140433972,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433972},{"clinical_significance":[],"seq_region_name":"7","id":"rs1249031100","alleles":["C","T"],"end":140433975,"feature_type":"variation","strand":1,"source":"dbSNP","start":140433975,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"id":"rs1799757132","seq_region_name":"7","clinical_significance":[],"alleles":["A","C","G"],"end":140433976,"strand":1,"feature_type":"variation","start":140433976,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1448193148","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140433979,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433979,"source":"dbSNP"},{"id":"rs555598660","seq_region_name":"7","clinical_significance":[],"start":140433981,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140433981,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799757207","source":"dbSNP","start":140433982,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140433982,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585443572","feature_type":"variation","strand":1,"end":140433983,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140433983},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130192896","source":"dbSNP","start":140433987,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140433987,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1585443575","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433992,"source":"dbSNP","strand":1,"feature_type":"variation","end":140433992,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799757247","source":"dbSNP","start":140433996,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140433996,"alleles":["G","A","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1312016864","clinical_significance":[],"end":140433997,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140433997,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140433999,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140433999,"source":"dbSNP","seq_region_name":"7","id":"rs113575494","clinical_significance":[]},{"seq_region_name":"7","id":"rs142385543","clinical_significance":[],"end":140434000,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140434000,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"start":140434003,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","C"],"end":140434003,"strand":1,"feature_type":"variation","id":"rs1799757380","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1266404577","clinical_significance":[],"alleles":["G","A"],"end":140434006,"strand":1,"feature_type":"variation","start":140434006,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140434007,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434007,"clinical_significance":[],"id":"rs2130192930","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130192933","source":"dbSNP","start":140434008,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140434008,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1799757409","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434012,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140434012},{"id":"rs909147587","seq_region_name":"7","clinical_significance":[],"start":140434013,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140434013,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1368209806","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140434015,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434015,"source":"dbSNP"},{"seq_region_name":"7","id":"rs767880768","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140434016,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434016,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140434029,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434029,"source":"dbSNP","id":"rs572089451","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434029,"feature_type":"variation","strand":1,"end":140434029,"alleles":["A","AA"],"clinical_significance":[],"id":"rs1799757521","seq_region_name":"7"},{"seq_region_name":"7","id":"rs545606299","clinical_significance":[],"start":140434030,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140434030,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434031,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140434031,"seq_region_name":"7","id":"rs2130192962","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434032,"feature_type":"variation","strand":1,"end":140434032,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799757557"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434034,"feature_type":"variation","strand":1,"end":140434034,"alleles":["C","A","T"],"clinical_significance":[],"id":"rs972052852","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1321415550","clinical_significance":[],"strand":1,"feature_type":"variation","end":140434035,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434035,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1745367225","end":140434042,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140434042,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799757613","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434044,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140434044},{"start":140434049,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140434049,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1020423750","clinical_significance":[]},{"id":"rs1799757663","seq_region_name":"7","clinical_significance":[],"start":140434052,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140434052,"alleles":["G","C","T"],"strand":1,"feature_type":"variation"},{"start":140434057,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140434057,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799757684","clinical_significance":[]},{"id":"rs1799757703","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140434058,"alleles":["C","A","G","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434058,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140434059,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434059,"clinical_significance":[],"id":"rs1449503437","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799757791","clinical_significance":[],"alleles":["G","A","C"],"end":140434061,"strand":1,"feature_type":"variation","start":140434061,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs933410692","clinical_significance":[],"start":140434067,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140434067,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140434068,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434068,"source":"dbSNP","seq_region_name":"7","id":"rs1799757832","clinical_significance":[]},{"source":"dbSNP","start":140434069,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140434069,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1050436820"},{"end":140434074,"alleles":["AAAAA","AAAA"],"strand":1,"feature_type":"variation","start":140434070,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1427833357","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799757877","clinical_significance":[],"alleles":["A","T"],"end":140434081,"strand":1,"feature_type":"variation","start":140434081,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140434086,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434086,"clinical_significance":[],"seq_region_name":"7","id":"rs1192362889"},{"clinical_significance":[],"seq_region_name":"7","id":"rs907458828","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434088,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140434088},{"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140434089,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434089,"clinical_significance":[],"seq_region_name":"7","id":"rs1418417953"},{"end":140434092,"alleles":["C","A","G"],"strand":1,"feature_type":"variation","start":140434092,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1486650761","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434093,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140434093,"seq_region_name":"7","id":"rs1799757970","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140434094,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434094,"clinical_significance":[],"seq_region_name":"7","id":"rs1003089866"},{"id":"rs1188077141","seq_region_name":"7","clinical_significance":[],"start":140434099,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A","C"],"end":140434099,"strand":1,"feature_type":"variation"},{"end":140434101,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140434101,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs2130193035","clinical_significance":[]},{"start":140434102,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140434102,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","id":"rs1034589847","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434104,"source":"dbSNP","strand":1,"feature_type":"variation","end":140434104,"alleles":["C","T"],"seq_region_name":"7","id":"rs1305469170","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585443621","clinical_significance":[],"start":140434105,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140434105,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140434109,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434109,"clinical_significance":[],"seq_region_name":"7","id":"rs958387067"},{"strand":1,"feature_type":"variation","end":140434110,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434110,"source":"dbSNP","id":"rs1369944105","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1459681602","clinical_significance":[],"end":140434111,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140434111,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"strand":1,"feature_type":"variation","end":140434115,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434115,"source":"dbSNP","seq_region_name":"7","id":"rs936859002","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140434120,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434120,"source":"dbSNP","seq_region_name":"7","id":"rs143293832","clinical_significance":[]},{"clinical_significance":[],"id":"rs892722497","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434121,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140434121},{"end":140434123,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140434123,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs781631908","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799758303","clinical_significance":[],"end":140434124,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140434124,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434127,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140434127,"id":"rs1799758316","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140434133,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140434133,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799758335"},{"clinical_significance":[],"id":"rs1799758357","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["GG","GGG"],"end":140434134,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434133},{"alleles":["G","A"],"end":140434134,"strand":1,"feature_type":"variation","start":140434134,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1799758379","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs576150330","clinical_significance":[],"strand":1,"feature_type":"variation","end":140434137,"alleles":["A","C","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434137,"source":"dbSNP"},{"start":140434141,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140434141,"alleles":["G","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1019963398","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434142,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140434142,"seq_region_name":"7","id":"rs1361286338","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585443649","clinical_significance":[],"end":140434147,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140434147,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1333436250","clinical_significance":[],"alleles":["C","A","T"],"end":140434148,"strand":1,"feature_type":"variation","start":140434148,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434151,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140434151,"clinical_significance":[],"seq_region_name":"7","id":"rs1371897475"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1454226440","alleles":["G","T"],"end":140434153,"feature_type":"variation","strand":1,"source":"dbSNP","start":140434153,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140434157,"alleles":["A","C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434157,"clinical_significance":[],"seq_region_name":"7","id":"rs1393897893"},{"clinical_significance":[],"seq_region_name":"7","id":"rs906831217","alleles":["G","T"],"end":140434158,"feature_type":"variation","strand":1,"source":"dbSNP","start":140434158,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140434163,"alleles":["T","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434163,"clinical_significance":[],"seq_region_name":"7","id":"rs1585443658"},{"seq_region_name":"7","id":"rs1429817299","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140434164,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434164,"source":"dbSNP"},{"source":"dbSNP","start":140434168,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140434168,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1259203205"},{"end":140434173,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140434173,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1799758602","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1204207191","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434174,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140434174},{"alleles":["G","A"],"end":140434175,"feature_type":"variation","strand":1,"source":"dbSNP","start":140434175,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130193123"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1002530194","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434177,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140434177},{"seq_region_name":"7","id":"rs1799758651","clinical_significance":[],"strand":1,"feature_type":"variation","end":140434180,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434180,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1034141895","seq_region_name":"7","alleles":["G","A"],"end":140434183,"feature_type":"variation","strand":1,"source":"dbSNP","start":140434183,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"id":"rs1208563980","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140434185,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434185,"source":"dbSNP"},{"alleles":["A","C","T"],"end":140434186,"strand":1,"feature_type":"variation","start":140434186,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1347037624","clinical_significance":[]},{"seq_region_name":"7","id":"rs1275350000","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434187,"source":"dbSNP","strand":1,"feature_type":"variation","end":140434187,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1229670079","alleles":["T","C"],"end":140434188,"feature_type":"variation","strand":1,"source":"dbSNP","start":140434188,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434191,"source":"dbSNP","strand":1,"feature_type":"variation","end":140434191,"alleles":["A","C"],"id":"rs1585443683","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434192,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140434192,"clinical_significance":[],"seq_region_name":"7","id":"rs1324814542"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585443687","feature_type":"variation","strand":1,"end":140434194,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434194},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799758813","source":"dbSNP","start":140434195,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140434195,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1313946851","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434198,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140434198},{"strand":1,"feature_type":"variation","end":140434205,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434205,"source":"dbSNP","seq_region_name":"7","id":"rs2130193153","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434208,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140434208,"seq_region_name":"7","id":"rs1799758856","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["TG","-"],"end":140434209,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434208,"source":"dbSNP","seq_region_name":"7","id":"rs2130193157","clinical_significance":[]},{"seq_region_name":"7","id":"rs1396861575","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434212,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140434212},{"id":"rs983029040","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434213,"source":"dbSNP","strand":1,"feature_type":"variation","end":140434213,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1311457985","source":"dbSNP","start":140434215,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140434215,"alleles":["G","A","T"],"feature_type":"variation","strand":1},{"start":140434217,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140434217,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799758908","clinical_significance":[]},{"source":"dbSNP","start":140434218,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140434218,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs776984958","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1171091707","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140434219,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434219,"source":"dbSNP"},{"end":140434221,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140434221,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1463026226"},{"seq_region_name":"7","id":"rs1799758999","clinical_significance":[],"start":140434222,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140434222,"strand":1,"feature_type":"variation"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434223,"feature_type":"variation","strand":1,"end":140434223,"alleles":["C","A","T"],"clinical_significance":[],"id":"rs1370873510","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799759033","clinical_significance":[],"start":140434224,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["-","A"],"end":140434223,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434224,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140434224,"seq_region_name":"7","id":"rs1424039778","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1318016447","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434225,"feature_type":"variation","strand":1,"alleles":["-","A","AA"],"end":140434224},{"clinical_significance":[],"id":"rs1259247768","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434225,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140434225},{"id":"rs1799759100","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140434225,"alleles":["C","-"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434225,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140434226,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434226,"source":"dbSNP","seq_region_name":"7","id":"rs1200045771","clinical_significance":[]},{"source":"dbSNP","start":140434226,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140434244,"alleles":["AAAAAAAAAAAAAAAAAAA","AAAAAA","AAAAAAAAAA","AAAAAAAAAAA","AAAAAAAAAAAA","AAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAA"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1245723650"},{"strand":1,"feature_type":"variation","end":140434235,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434235,"source":"dbSNP","seq_region_name":"7","id":"rs1414527578","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563078775","alleles":["-","G"],"end":140434235,"feature_type":"variation","strand":1,"source":"dbSNP","start":140434236,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"alleles":["A","G"],"end":140434236,"strand":1,"feature_type":"variation","start":140434236,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs985059514","clinical_significance":[]},{"id":"rs1585443729","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140434237,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434237,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434240,"source":"dbSNP","strand":1,"feature_type":"variation","end":140434240,"alleles":["A","G"],"seq_region_name":"7","id":"rs1799759338","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799759353","alleles":["A","AGA"],"end":140434241,"feature_type":"variation","strand":1,"source":"dbSNP","start":140434241,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434243,"feature_type":"variation","strand":1,"end":140434243,"alleles":["A","AGA"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585443734"},{"end":140434244,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140434244,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1331413069"},{"seq_region_name":"7","id":"rs764579076","clinical_significance":[],"end":140434245,"alleles":["G","-"],"strand":1,"feature_type":"variation","start":140434245,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1190441401","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140434245,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434245,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799759421","clinical_significance":[],"start":140434246,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["ATGGA","ATGGAATGGA"],"end":140434250,"strand":1,"feature_type":"variation"},{"start":140434247,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140434247,"alleles":["T","A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1480288961","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585443745","feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140434248,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434248},{"clinical_significance":[],"seq_region_name":"7","id":"rs912358673","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434250,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140434250},{"seq_region_name":"7","id":"rs1390170476","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434251,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140434251},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434254,"source":"dbSNP","strand":1,"feature_type":"variation","end":140434254,"alleles":["T","C","G"],"seq_region_name":"7","id":"rs543453243","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434255,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140434255,"clinical_significance":[],"seq_region_name":"7","id":"rs962288027"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130193271","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434261,"feature_type":"variation","strand":1,"end":140434261,"alleles":["G","T"]},{"end":140434267,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140434267,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs971917096"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1419537710","source":"dbSNP","start":140434273,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140434273,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434275,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140434275,"seq_region_name":"7","id":"rs975335776","clinical_significance":[]},{"start":140434284,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140434286,"alleles":["TCT","T"],"strand":1,"feature_type":"variation","id":"rs1162415864","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1474731429","feature_type":"variation","strand":1,"end":140434287,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434287},{"start":140434291,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140434291,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1421789425","clinical_significance":[]},{"id":"rs1799759671","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140434295,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434295,"source":"dbSNP"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434298,"feature_type":"variation","strand":1,"end":140434298,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs117270485"},{"clinical_significance":[],"seq_region_name":"7","id":"rs933358347","source":"dbSNP","start":140434299,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140434299,"alleles":["T","A","C"],"feature_type":"variation","strand":1},{"start":140434302,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140434302,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs1585443781","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1249802799","alleles":["C","T"],"end":140434305,"feature_type":"variation","strand":1,"source":"dbSNP","start":140434305,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"start":140434306,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140434306,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs148348211","clinical_significance":[]},{"clinical_significance":[],"id":"rs1585443783","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434307,"feature_type":"variation","strand":1,"end":140434307,"alleles":["C","T"]},{"feature_type":"variation","strand":1,"end":140434310,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434310,"clinical_significance":[],"id":"rs541186778","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140434320,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434320,"source":"dbSNP","seq_region_name":"7","id":"rs1799759849","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434322,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140434322,"seq_region_name":"7","id":"rs910656755","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130193314","clinical_significance":[],"start":140434324,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140434324,"alleles":["T","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1271451939","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140434325,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434325},{"alleles":["T","C"],"end":140434326,"strand":1,"feature_type":"variation","start":140434326,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1232930346","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs936739397","clinical_significance":[],"strand":1,"feature_type":"variation","end":140434328,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434328,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799759913","source":"dbSNP","start":140434335,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140434335,"alleles":["A","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1054380737","clinical_significance":[],"start":140434337,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140434337,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140434344,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434344,"clinical_significance":[],"seq_region_name":"7","id":"rs1237407305"},{"source":"dbSNP","start":140434345,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140434345,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1054363475"},{"seq_region_name":"7","id":"rs1799759979","clinical_significance":[],"strand":1,"feature_type":"variation","end":140434347,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434347,"source":"dbSNP"},{"start":140434349,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140434349,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799759999","clinical_significance":[]},{"end":140434351,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140434351,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1172964677"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130193341","feature_type":"variation","strand":1,"end":140434353,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434353},{"clinical_significance":[],"id":"rs1352816643","seq_region_name":"7","source":"dbSNP","start":140434355,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140434355,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799760052","source":"dbSNP","start":140434355,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["GGCCCCTGG","GG"],"end":140434363,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130193345","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434356,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140434356},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434357,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140434357,"clinical_significance":[],"seq_region_name":"7","id":"rs1324823860"},{"strand":1,"feature_type":"variation","end":140434358,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434358,"source":"dbSNP","seq_region_name":"7","id":"rs1440981750","clinical_significance":[]},{"alleles":["G","T"],"end":140434362,"strand":1,"feature_type":"variation","start":140434362,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1799760095","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434363,"feature_type":"variation","strand":1,"end":140434363,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1396065134"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434364,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140434364,"id":"rs1323432865","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs914656786","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434366,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140434366},{"feature_type":"variation","strand":1,"end":140434367,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434367,"clinical_significance":[],"seq_region_name":"7","id":"rs1461941232"},{"seq_region_name":"7","id":"rs2130193366","clinical_significance":[],"start":140434368,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140434368,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1799760173","clinical_significance":[],"end":140434372,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140434372,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434374,"source":"dbSNP","strand":1,"feature_type":"variation","end":140434374,"alleles":["C","G"],"id":"rs1799760200","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1303898324","clinical_significance":[],"alleles":["C","T"],"end":140434376,"strand":1,"feature_type":"variation","start":140434376,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1799760244","clinical_significance":[],"strand":1,"feature_type":"variation","end":140434386,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434386,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140434396,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434396,"source":"dbSNP","seq_region_name":"7","id":"rs200328952","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434397,"source":"dbSNP","strand":1,"feature_type":"variation","end":140434397,"alleles":["T","-"],"seq_region_name":"7","id":"rs1799760288","clinical_significance":[]},{"seq_region_name":"7","id":"rs17161542","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434409,"source":"dbSNP","strand":1,"feature_type":"variation","end":140434409,"alleles":["T","C","G"]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434411,"feature_type":"variation","strand":1,"end":140434411,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130193400"},{"clinical_significance":[],"id":"rs2130193405","seq_region_name":"7","feature_type":"variation","strand":1,"end":140434412,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434412},{"start":140434413,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140434413,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs914032677","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434418,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140434418,"seq_region_name":"7","id":"rs1799760396","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799760413","clinical_significance":[],"start":140434419,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140434419,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140434423,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434423,"clinical_significance":[],"id":"rs945617397","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799760441","clinical_significance":[],"strand":1,"feature_type":"variation","end":140434424,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434424,"source":"dbSNP"},{"alleles":["G","A"],"end":140434427,"strand":1,"feature_type":"variation","start":140434427,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1585443829","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799760478","feature_type":"variation","strand":1,"end":140434432,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434432},{"seq_region_name":"7","id":"rs1413257686","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434433,"source":"dbSNP","strand":1,"feature_type":"variation","end":140434433,"alleles":["T","A"]},{"clinical_significance":[],"id":"rs1042283737","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434434,"feature_type":"variation","strand":1,"end":140434434,"alleles":["G","A","C"]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434436,"source":"dbSNP","strand":1,"feature_type":"variation","end":140434436,"alleles":["G","T"],"seq_region_name":"7","id":"rs1585443834","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799760550","feature_type":"variation","strand":1,"end":140434437,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434437},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140434441,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434441,"source":"dbSNP","id":"rs1251221752","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799760566","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140434442,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434442},{"alleles":["T","A"],"end":140434447,"strand":1,"feature_type":"variation","start":140434447,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1340816389","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1213233544","alleles":["G","A"],"end":140434448,"feature_type":"variation","strand":1,"source":"dbSNP","start":140434448,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1465500934","source":"dbSNP","start":140434452,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140434452,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1220054948","feature_type":"variation","strand":1,"end":140434456,"alleles":["C","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434456},{"end":140434457,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140434457,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799760666"},{"clinical_significance":[],"seq_region_name":"7","id":"rs533443709","end":140434458,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140434458,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434459,"feature_type":"variation","strand":1,"end":140434459,"alleles":["G","A","C","T"],"clinical_significance":[],"id":"rs551623477","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799760755","clinical_significance":[],"end":140434463,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140434463,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"start":140434467,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","G","T"],"end":140434467,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1002566118","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1003437558","feature_type":"variation","strand":1,"end":140434471,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434471},{"seq_region_name":"7","id":"rs1372461467","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434472,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140434472},{"seq_region_name":"7","id":"rs73163263","clinical_significance":[],"end":140434474,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140434474,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434479,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140434479,"clinical_significance":[],"seq_region_name":"7","id":"rs1799760852"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434485,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140434485,"seq_region_name":"7","id":"rs1799760869","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799760886","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140434486,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434486,"source":"dbSNP"},{"alleles":["G","C"],"end":140434487,"strand":1,"feature_type":"variation","start":140434487,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs894231155","clinical_significance":[]},{"clinical_significance":[],"id":"rs10256899","seq_region_name":"7","source":"dbSNP","start":140434489,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140434489,"alleles":["A","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs995183962","end":140434490,"alleles":["G","C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140434490,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1799761029","clinical_significance":[],"strand":1,"feature_type":"variation","end":140434494,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434494,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799761049","feature_type":"variation","strand":1,"end":140434495,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434495},{"seq_region_name":"7","id":"rs1799761068","clinical_significance":[],"start":140434497,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140434497,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1384012868","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434499,"feature_type":"variation","strand":1,"end":140434499,"alleles":["T","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1174109194","end":140434500,"alleles":["G","GG"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140434500,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799761109","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434500,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140434500},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434505,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140434505,"seq_region_name":"7","id":"rs1026616503","clinical_significance":[]},{"end":140434509,"alleles":["G","C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140434509,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1563078857","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1393253101","alleles":["G","A","C"],"end":140434525,"feature_type":"variation","strand":1,"source":"dbSNP","start":140434525,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140434534,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434534,"source":"dbSNP","seq_region_name":"7","id":"rs1482229854","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140434535,"alleles":["C","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434535,"clinical_significance":[],"id":"rs1209980665","seq_region_name":"7"},{"id":"rs2130193531","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140434536,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434536,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1475803687","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434543,"source":"dbSNP","strand":1,"feature_type":"variation","end":140434543,"alleles":["C","A"]},{"start":140434552,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","T"],"end":140434552,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1244035432","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs141547044","alleles":["A","C"],"end":140434555,"feature_type":"variation","strand":1,"source":"dbSNP","start":140434555,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"id":"rs1446748671","seq_region_name":"7","clinical_significance":[],"end":140434558,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140434558,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140434560,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434560,"clinical_significance":[],"seq_region_name":"7","id":"rs1004000613"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1279793563","end":140434567,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140434567,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1799761354","seq_region_name":"7","source":"dbSNP","start":140434570,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140434570,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1019780122","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434571,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140434571},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434572,"source":"dbSNP","strand":1,"feature_type":"variation","end":140434572,"alleles":["G","A"],"seq_region_name":"7","id":"rs1585443908","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140434573,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434573,"source":"dbSNP","seq_region_name":"7","id":"rs117263574","clinical_significance":[]},{"source":"dbSNP","start":140434576,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140434576,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799761452"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434581,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140434581,"seq_region_name":"7","id":"rs567584271","clinical_significance":[]},{"end":140434586,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140434586,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799761496"},{"seq_region_name":"7","id":"rs1417499004","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434588,"source":"dbSNP","strand":1,"feature_type":"variation","end":140434588,"alleles":["A","G"]},{"source":"dbSNP","start":140434591,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140434591,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs150477003"},{"seq_region_name":"7","id":"rs1799761561","clinical_significance":[],"strand":1,"feature_type":"variation","end":140434594,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434594,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799761577","alleles":["T","G"],"end":140434597,"feature_type":"variation","strand":1,"source":"dbSNP","start":140434597,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434600,"feature_type":"variation","strand":1,"end":140434600,"alleles":["G","A"],"clinical_significance":[],"id":"rs975202931","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140434603,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434603,"source":"dbSNP","seq_region_name":"7","id":"rs1232889975","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799761643","seq_region_name":"7","source":"dbSNP","start":140434612,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140434612,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140434613,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","A","G","T"],"end":140434613,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs762605050","seq_region_name":"7"},{"alleles":["T","C"],"end":140434617,"strand":1,"feature_type":"variation","start":140434617,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs563262260","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140434618,"alleles":["T","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434618,"clinical_significance":[],"id":"rs1030227894","seq_region_name":"7"},{"source":"dbSNP","start":140434625,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140434629,"alleles":["AAAAA","AAAA"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1271530368","seq_region_name":"7"},{"end":140434630,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140434630,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs369402312","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799761756","source":"dbSNP","start":140434635,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140434635,"alleles":["G","T"],"feature_type":"variation","strand":1},{"alleles":["C","T"],"end":140434637,"strand":1,"feature_type":"variation","start":140434637,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs954614918","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434638,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140434638,"id":"rs1313244828","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140434639,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140434639,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs184610401"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799761840","source":"dbSNP","start":140434642,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140434642,"alleles":["C","G","T"],"feature_type":"variation","strand":1},{"start":140434643,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140434643,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs6954173","clinical_significance":[]},{"id":"rs990110778","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434644,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140434644},{"clinical_significance":[],"seq_region_name":"7","id":"rs1312695213","end":140434645,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140434645,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"alleles":["G","A"],"end":140434646,"strand":1,"feature_type":"variation","start":140434646,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1361541788","clinical_significance":[]},{"seq_region_name":"7","id":"rs1166306922","clinical_significance":[],"start":140434652,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","A"],"end":140434652,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140434654,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434654,"clinical_significance":[],"seq_region_name":"7","id":"rs1401482587"},{"clinical_significance":[],"seq_region_name":"7","id":"rs6968931","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434656,"feature_type":"variation","strand":1,"end":140434656,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs946028874","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434659,"source":"dbSNP","strand":1,"feature_type":"variation","end":140434659,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1190507926","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434662,"feature_type":"variation","strand":1,"end":140434662,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799762096","alleles":["C","T"],"end":140434665,"feature_type":"variation","strand":1,"source":"dbSNP","start":140434665,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799762106","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140434666,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434666},{"clinical_significance":[],"seq_region_name":"7","id":"rs1360663026","source":"dbSNP","start":140434668,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140434668,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs989544548","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434670,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140434670},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434671,"feature_type":"variation","strand":1,"end":140434671,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1206539375"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799762200","end":140434687,"alleles":["GAGGCCGAGGC","GAGGC"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140434677,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799762216","source":"dbSNP","start":140434679,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140434679,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1799762242","clinical_significance":[],"end":140434679,"alleles":["-","C"],"strand":1,"feature_type":"variation","start":140434680,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140434681,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434681,"source":"dbSNP","seq_region_name":"7","id":"rs1041831542","clinical_significance":[]},{"seq_region_name":"7","id":"rs542247818","clinical_significance":[],"start":140434681,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["CC","C"],"end":140434682,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1212348819","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434682,"feature_type":"variation","strand":1,"end":140434682,"alleles":["C","G","T"]},{"seq_region_name":"7","id":"rs913964315","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434683,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140434683},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585443975","feature_type":"variation","strand":1,"end":140434685,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434685},{"clinical_significance":[],"seq_region_name":"7","id":"rs1293566824","feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140434687,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434687},{"start":140434688,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A","T"],"end":140434688,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs540854856","clinical_significance":[]},{"alleles":["GGG","GG"],"end":140434690,"strand":1,"feature_type":"variation","start":140434688,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1799762384","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs899864113","clinical_significance":[],"start":140434691,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140434691,"alleles":["T","A","C","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1356299865","end":140434692,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140434692,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140434694,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140434694,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130193708"},{"alleles":["T","A"],"end":140434695,"strand":1,"feature_type":"variation","start":140434695,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1168410972","clinical_significance":[]},{"source":"dbSNP","start":140434695,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140434705,"alleles":["TCATGAGGTCA","TCA"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799762476"},{"alleles":["C","A"],"end":140434696,"feature_type":"variation","strand":1,"source":"dbSNP","start":140434696,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs938846692"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140434698,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434698,"source":"dbSNP","seq_region_name":"7","id":"rs1418809123","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434699,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140434699,"id":"rs1055950291","seq_region_name":"7","clinical_significance":[]},{"end":140434702,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140434702,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799762554","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1011955799","source":"dbSNP","start":140434703,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140434703,"alleles":["T","G"],"feature_type":"variation","strand":1},{"id":"rs1167436160","seq_region_name":"7","clinical_significance":[],"start":140434704,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140434704,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140434706,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434706,"clinical_significance":[],"id":"rs1474403463","seq_region_name":"7"},{"end":140434707,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140434707,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs367907002"},{"seq_region_name":"7","id":"rs1178223162","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434709,"source":"dbSNP","strand":1,"feature_type":"variation","end":140434709,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1481898828","clinical_significance":[],"alleles":["T","C","G"],"end":140434711,"strand":1,"feature_type":"variation","start":140434711,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1046585161","source":"dbSNP","start":140434712,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","A","G","T"],"end":140434712,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140434713,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434713,"source":"dbSNP","seq_region_name":"7","id":"rs1286502088","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs928232937","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140434714,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434714},{"seq_region_name":"7","id":"rs1219081936","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140434715,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434715,"source":"dbSNP"},{"seq_region_name":"7","id":"rs537016660","clinical_significance":[],"strand":1,"feature_type":"variation","end":140434732,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434732,"source":"dbSNP"},{"alleles":["A","G"],"end":140434733,"feature_type":"variation","strand":1,"source":"dbSNP","start":140434733,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs555418672","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434734,"source":"dbSNP","strand":1,"feature_type":"variation","end":140434734,"alleles":["G","A"],"seq_region_name":"7","id":"rs886817318","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140434735,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434735,"source":"dbSNP","seq_region_name":"7","id":"rs1799762882","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1292467337","feature_type":"variation","strand":1,"end":140434739,"alleles":["A","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434739},{"clinical_significance":[],"seq_region_name":"7","id":"rs1224191184","source":"dbSNP","start":140434741,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140434741,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1004267715","alleles":["C","T"],"end":140434742,"feature_type":"variation","strand":1,"source":"dbSNP","start":140434742,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1019388583","source":"dbSNP","start":140434744,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140434744,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799762965","alleles":["C","G","T"],"end":140434751,"feature_type":"variation","strand":1,"source":"dbSNP","start":140434751,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140434753,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434753,"clinical_significance":[],"id":"rs1585444018","seq_region_name":"7"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434757,"feature_type":"variation","strand":1,"end":140434757,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs894103184"},{"alleles":["T","C"],"end":140434758,"strand":1,"feature_type":"variation","start":140434758,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1269514537","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs189392646","clinical_significance":[],"end":140434760,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140434760,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1799763097","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434761,"source":"dbSNP","strand":1,"feature_type":"variation","end":140434761,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs1328093496","clinical_significance":[],"alleles":["A","T"],"end":140434762,"strand":1,"feature_type":"variation","start":140434762,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"start":140434763,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","C"],"end":140434763,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1037489949","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799763167","end":140434769,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140434769,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1799763178","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140434770,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434770,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799763200","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434771,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140434771},{"alleles":["T","C"],"end":140434772,"feature_type":"variation","strand":1,"source":"dbSNP","start":140434772,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799763214","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1799763236","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434776,"feature_type":"variation","strand":1,"end":140434776,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1394096133","clinical_significance":[],"start":140434778,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140434778,"alleles":["A","C","T"],"strand":1,"feature_type":"variation"},{"end":140434779,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140434779,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1160281815","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799763271","source":"dbSNP","start":140434781,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140434781,"feature_type":"variation","strand":1},{"id":"rs1173508336","seq_region_name":"7","clinical_significance":[],"alleles":["A","G"],"end":140434782,"strand":1,"feature_type":"variation","start":140434782,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1381352209","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434784,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140434784},{"seq_region_name":"7","id":"rs180725559","clinical_significance":[],"end":140434785,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140434785,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1177156656","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434786,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140434786},{"start":140434788,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140434788,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1028072938","clinical_significance":[]},{"clinical_significance":[],"id":"rs1253092254","seq_region_name":"7","feature_type":"variation","strand":1,"end":140434789,"alleles":["G","A","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434789},{"seq_region_name":"7","id":"rs957955027","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434790,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140434790},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434794,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140434794,"seq_region_name":"7","id":"rs1799763390","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1156508018","source":"dbSNP","start":140434795,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140434795,"alleles":["A","G"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140434796,"alleles":["G","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434796,"clinical_significance":[],"id":"rs1466852071","seq_region_name":"7"},{"seq_region_name":"7","id":"rs989388930","clinical_significance":[],"strand":1,"feature_type":"variation","end":140434799,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434799,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434805,"source":"dbSNP","strand":1,"feature_type":"variation","end":140434805,"alleles":["A","G"],"seq_region_name":"7","id":"rs1799763463","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140434807,"alleles":["T","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434807,"clinical_significance":[],"id":"rs1021286810","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434808,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140434808,"seq_region_name":"7","id":"rs1799763492","clinical_significance":[]},{"source":"dbSNP","start":140434809,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140434809,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs374077694"},{"seq_region_name":"7","id":"rs1318554496","clinical_significance":[],"start":140434813,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140434813,"alleles":["G","A","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1304724869","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434814,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140434814},{"id":"rs967435352","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434815,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140434815},{"clinical_significance":[],"id":"rs1585444051","seq_region_name":"7","alleles":["T","C"],"end":140434816,"feature_type":"variation","strand":1,"source":"dbSNP","start":140434816,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"alleles":["G","A"],"end":140434819,"feature_type":"variation","strand":1,"source":"dbSNP","start":140434819,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799763615","seq_region_name":"7"},{"start":140434820,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140434820,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130193879","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140434822,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434822,"source":"dbSNP","seq_region_name":"7","id":"rs377388320","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434823,"feature_type":"variation","strand":1,"end":140434823,"alleles":["G","A"],"clinical_significance":[],"id":"rs1799763651","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140434824,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434824,"clinical_significance":[],"seq_region_name":"7","id":"rs559489801"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434826,"source":"dbSNP","strand":1,"feature_type":"variation","end":140434826,"alleles":["G","A","T"],"seq_region_name":"7","id":"rs796387764","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs938710417","source":"dbSNP","start":140434829,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140434829,"feature_type":"variation","strand":1},{"alleles":["G","A"],"end":140434830,"feature_type":"variation","strand":1,"source":"dbSNP","start":140434830,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1370484180"},{"seq_region_name":"7","id":"rs1563078917","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434832,"source":"dbSNP","strand":1,"feature_type":"variation","end":140434832,"alleles":["C","T"]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434833,"feature_type":"variation","strand":1,"end":140434832,"alleles":["-","CT"],"clinical_significance":[],"seq_region_name":"7","id":"rs1563078921"},{"strand":1,"feature_type":"variation","end":140434833,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434833,"source":"dbSNP","seq_region_name":"7","id":"rs1018028232","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140434834,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434834,"clinical_significance":[],"id":"rs958097218","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140434837,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434837,"clinical_significance":[],"seq_region_name":"7","id":"rs1585444067"},{"seq_region_name":"7","id":"rs1799763842","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434838,"source":"dbSNP","strand":1,"feature_type":"variation","end":140434838,"alleles":["C","T"]},{"start":140434838,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140434841,"alleles":["CCCC","CCC"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799763922","clinical_significance":[]},{"alleles":["C","T"],"end":140434839,"strand":1,"feature_type":"variation","start":140434839,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1799763944","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs991665424","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434840,"feature_type":"variation","strand":1,"end":140434840,"alleles":["C","T"]},{"id":"rs1799763978","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140434841,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434841,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1309810748","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["GGGGGG","GGGGG","GGGGGGG"],"end":140434847,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434842,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1021059981","feature_type":"variation","strand":1,"end":140434843,"alleles":["G","C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434843},{"seq_region_name":"7","id":"rs1221918324","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434844,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140434844},{"seq_region_name":"7","id":"rs1799764074","clinical_significance":[],"start":140434845,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140434845,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140434846,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140434846,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1283284973"},{"seq_region_name":"7","id":"rs916116633","clinical_significance":[],"start":140434847,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140434847,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs931467164","end":140434848,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140434848,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140434849,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434849,"clinical_significance":[],"seq_region_name":"7","id":"rs1222551239"},{"seq_region_name":"7","id":"rs1799764166","clinical_significance":[],"start":140434851,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140434851,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"start":140434854,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140434854,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799764176","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140434855,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434855,"clinical_significance":[],"id":"rs1799764194","seq_region_name":"7"},{"source":"dbSNP","start":140434857,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140434857,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799764211"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434866,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140434866,"clinical_significance":[],"seq_region_name":"7","id":"rs1275151470"},{"end":140434871,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140434871,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs966774440","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799764265","clinical_significance":[],"strand":1,"feature_type":"variation","end":140434872,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434872,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140434873,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434873,"clinical_significance":[],"id":"rs2130193971","seq_region_name":"7"},{"end":140434874,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140434874,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1486701776","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799764287","source":"dbSNP","start":140434880,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140434880,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1258752146","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434883,"source":"dbSNP","strand":1,"feature_type":"variation","end":140434883,"alleles":["C","G","T"]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434884,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140434884,"clinical_significance":[],"seq_region_name":"7","id":"rs1193562426"},{"source":"dbSNP","start":140434886,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140434886,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs982290906"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1442083322","feature_type":"variation","strand":1,"end":140434887,"alleles":["A","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434887},{"alleles":["T","C"],"end":140434891,"strand":1,"feature_type":"variation","start":140434891,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1048664553","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799764398","clinical_significance":[],"strand":1,"feature_type":"variation","end":140434893,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434893,"source":"dbSNP"},{"id":"rs1799764421","seq_region_name":"7","clinical_significance":[],"start":140434894,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140434894,"alleles":["G","A","T"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140434895,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434895,"source":"dbSNP","id":"rs928095526","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434896,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140434896,"clinical_significance":[],"seq_region_name":"7","id":"rs1407690219"},{"seq_region_name":"7","id":"rs1799764471","clinical_significance":[],"end":140434900,"alleles":["AG","AGAG"],"strand":1,"feature_type":"variation","start":140434899,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"id":"rs1563078938","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434900,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GGG","GG"],"end":140434902},{"id":"rs1799764512","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140434900,"alleles":["-","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434901,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585444110","alleles":["G","C"],"end":140434901,"feature_type":"variation","strand":1,"source":"dbSNP","start":140434901,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799764555","source":"dbSNP","start":140434902,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140434901,"alleles":["-","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs577722847","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140434902,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434902,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140434903,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434903,"source":"dbSNP","seq_region_name":"7","id":"rs1296512218","clinical_significance":[]},{"end":140434906,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140434906,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799764599","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799764615","feature_type":"variation","strand":1,"end":140434908,"alleles":["C","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434908},{"source":"dbSNP","start":140434910,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140434910,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1384135645"},{"feature_type":"variation","strand":1,"end":140434911,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434911,"clinical_significance":[],"id":"rs938247980","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1302821297","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["AAAAAAAA","-"],"end":140434922,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434915},{"end":140434922,"alleles":["AAAAAAAA","AAAAAAA","AAAAAAAAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140434915,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1405619379"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434916,"feature_type":"variation","strand":1,"alleles":["AAAAAAATAAAAAAATAAA","AAAAAAATAAA","AAAAAAATAAAAAAATAAAAAAATAAA"],"end":140434934,"clinical_significance":[],"seq_region_name":"7","id":"rs1166425486"},{"start":140434918,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140434918,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799764736","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585444122","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140434920,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434920,"source":"dbSNP"},{"end":140434921,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140434921,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1391661646"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1377769116","source":"dbSNP","start":140434923,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140434923,"alleles":["T","-"],"feature_type":"variation","strand":1},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434923,"feature_type":"variation","strand":1,"end":140434923,"alleles":["T","A"],"clinical_significance":[],"id":"rs1460417643","seq_region_name":"7"},{"source":"dbSNP","start":140434924,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140434924,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs991054417","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["AAAAAAA","AAAAAAAA"],"end":140434930,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434924,"source":"dbSNP","seq_region_name":"7","id":"rs1432272445","clinical_significance":[]},{"seq_region_name":"7","id":"rs545190863","clinical_significance":[],"end":140434927,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140434927,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"id":"rs1799764899","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434928,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AAATAAATAAA","AAATAAA"],"end":140434938},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140434930,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434930,"clinical_significance":[],"id":"rs939715196","seq_region_name":"7"},{"source":"dbSNP","start":140434931,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","-"],"end":140434931,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1429911603"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799764957","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434932,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140434932},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434932,"feature_type":"variation","strand":1,"end":140434934,"alleles":["AAA","AA","AAAA"],"clinical_significance":[],"id":"rs1259309670","seq_region_name":"7"},{"id":"rs1192627741","seq_region_name":"7","clinical_significance":[],"end":140434947,"alleles":["AAATAAAAATAAAAAT","AAATAAAAAT"],"strand":1,"feature_type":"variation","start":140434932,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"id":"rs1485904193","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","A"],"end":140434935,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434935},{"alleles":["AAATAAA","AAA"],"end":140434944,"feature_type":"variation","strand":1,"source":"dbSNP","start":140434938,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1259461366"},{"id":"rs1208674102","seq_region_name":"7","clinical_significance":[],"end":140434941,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140434941,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"feature_type":"variation","strand":1,"end":140434944,"alleles":["A","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434944,"clinical_significance":[],"id":"rs1799765068","seq_region_name":"7"},{"seq_region_name":"7","id":"rs749510881","clinical_significance":[],"alleles":["A","T"],"end":140434945,"strand":1,"feature_type":"variation","start":140434945,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799765102","end":140434946,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140434946,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"start":140434949,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140434949,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","id":"rs184480440","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434954,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140434954,"clinical_significance":[],"id":"rs1585444152","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140434956,"alleles":["C","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434956,"clinical_significance":[],"seq_region_name":"7","id":"rs1563078963"},{"id":"rs1439891344","seq_region_name":"7","clinical_significance":[],"start":140434960,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A","T"],"end":140434960,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs900932538","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434963,"feature_type":"variation","strand":1,"end":140434963,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1037760139","feature_type":"variation","strand":1,"end":140434965,"alleles":["G","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434965},{"start":140434966,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140434966,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1277853224","clinical_significance":[]},{"id":"rs1234258892","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140434967,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434967,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799765274","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434969,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140434969},{"seq_region_name":"7","id":"rs996516797","clinical_significance":[],"start":140434971,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140434971,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799765321","source":"dbSNP","start":140434975,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140434983,"alleles":["TCTGTAATC","TC"],"feature_type":"variation","strand":1},{"id":"rs1799765345","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434979,"source":"dbSNP","strand":1,"feature_type":"variation","end":140434979,"alleles":["T","C"]},{"end":140434982,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140434982,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1379556604","clinical_significance":[]},{"id":"rs6947449","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140434985,"alleles":["T","C","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140434985,"source":"dbSNP"},{"end":140434986,"alleles":["TG","CT"],"strand":1,"feature_type":"variation","start":140434985,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs386718461","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs60979188","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434986,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140434986},{"clinical_significance":[],"seq_region_name":"7","id":"rs560972171","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434990,"feature_type":"variation","strand":1,"end":140434990,"alleles":["C","T"]},{"source":"dbSNP","start":140434991,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140434993,"alleles":["TTT","TT"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1397902992"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434992,"feature_type":"variation","strand":1,"end":140434992,"alleles":["T","C"],"clinical_significance":[],"id":"rs1298245996","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140434998,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140434998,"clinical_significance":[],"id":"rs1799765466","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140435007,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140435007,"source":"dbSNP","id":"rs1799765500","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799765518","alleles":["G","A"],"end":140435008,"feature_type":"variation","strand":1,"source":"dbSNP","start":140435008,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"id":"rs1020886450","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140435010,"source":"dbSNP","strand":1,"feature_type":"variation","end":140435010,"alleles":["C","T"]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140435011,"source":"dbSNP","strand":1,"feature_type":"variation","end":140435011,"alleles":["G","A"],"seq_region_name":"7","id":"rs1051547391","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799765568","alleles":["G","GTCTG"],"end":140435011,"feature_type":"variation","strand":1,"source":"dbSNP","start":140435011,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs528775342","clinical_significance":[],"start":140435015,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","A"],"end":140435015,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140435018,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140435018,"source":"dbSNP","id":"rs1799765614","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435026,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140435026,"clinical_significance":[],"id":"rs1585444199","seq_region_name":"7"},{"end":140435029,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140435029,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799765648","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140435032,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435032,"clinical_significance":[],"seq_region_name":"7","id":"rs1585444203"},{"source":"dbSNP","start":140435033,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140435033,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799765688","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140435034,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435034,"clinical_significance":[],"seq_region_name":"7","id":"rs1799765703"},{"seq_region_name":"7","id":"rs1475388169","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140435036,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140435036},{"alleles":["G","A"],"end":140435040,"strand":1,"feature_type":"variation","start":140435040,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs890251413","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140435041,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435041,"clinical_significance":[],"seq_region_name":"7","id":"rs977453300"},{"source":"dbSNP","start":140435043,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140435043,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799765779"},{"alleles":["C","T"],"end":140435046,"strand":1,"feature_type":"variation","start":140435046,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs376339629","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799765814","clinical_significance":[],"start":140435048,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140435048,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1185633880","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140435050,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140435050},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435056,"feature_type":"variation","strand":1,"end":140435059,"alleles":["CCCC","CCC"],"clinical_significance":[],"seq_region_name":"7","id":"rs1563078992"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140435061,"source":"dbSNP","strand":1,"feature_type":"variation","end":140435061,"alleles":["T","C"],"seq_region_name":"7","id":"rs1799765852","clinical_significance":[]},{"id":"rs1036067440","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140435065,"source":"dbSNP","strand":1,"feature_type":"variation","end":140435065,"alleles":["T","A"]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435071,"feature_type":"variation","strand":1,"end":140435071,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1017558753"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435078,"feature_type":"variation","strand":1,"end":140435078,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799765929"},{"end":140435080,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140435080,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799765948"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1258760974","source":"dbSNP","start":140435082,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140435082,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs2130194222","clinical_significance":[],"end":140435085,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140435085,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"id":"rs1799765983","seq_region_name":"7","clinical_significance":[],"start":140435086,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","G"],"end":140435086,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1479729172","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435090,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140435090},{"clinical_significance":[],"seq_region_name":"7","id":"rs960022251","feature_type":"variation","strand":1,"end":140435092,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435092},{"clinical_significance":[],"id":"rs1799766033","seq_region_name":"7","end":140435094,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140435094,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1202977380","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140435098,"source":"dbSNP","strand":1,"feature_type":"variation","end":140435098,"alleles":["G","C"]},{"clinical_significance":[],"id":"rs1234167122","seq_region_name":"7","feature_type":"variation","strand":1,"end":140435099,"alleles":["T","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435099},{"start":140435100,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140435100,"alleles":["G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799766080","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799766097","feature_type":"variation","strand":1,"end":140435101,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435101},{"feature_type":"variation","strand":1,"alleles":["A","C","T"],"end":140435102,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435102,"clinical_significance":[],"seq_region_name":"7","id":"rs1337320461"},{"feature_type":"variation","strand":1,"end":140435105,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435105,"clinical_significance":[],"seq_region_name":"7","id":"rs1291839124"},{"clinical_significance":[],"id":"rs1244601519","seq_region_name":"7","source":"dbSNP","start":140435108,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140435108,"feature_type":"variation","strand":1},{"id":"rs1799766274","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140435109,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140435109},{"id":"rs547021103","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140435110,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140435110,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1309845041","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140435111,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140435111},{"feature_type":"variation","strand":1,"end":140435113,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435113,"clinical_significance":[],"seq_region_name":"7","id":"rs1799766348"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435114,"feature_type":"variation","strand":1,"end":140435114,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799766367"},{"clinical_significance":[],"seq_region_name":"7","id":"rs893694783","end":140435115,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140435115,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1010938341","alleles":["T","G"],"end":140435119,"feature_type":"variation","strand":1,"source":"dbSNP","start":140435119,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1021347042","clinical_significance":[],"start":140435123,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140435123,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140435124,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435124,"clinical_significance":[],"seq_region_name":"7","id":"rs1396301186"},{"start":140435131,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140435131,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","id":"rs991611681","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs966805620","seq_region_name":"7","end":140435133,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140435133,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"alleles":["A","T"],"end":140435135,"strand":1,"feature_type":"variation","start":140435135,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1799766658","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1364293485","clinical_significance":[],"end":140435138,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140435138,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs571919543","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140435142,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435142},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140435144,"source":"dbSNP","strand":1,"feature_type":"variation","end":140435144,"alleles":["C","T"],"seq_region_name":"7","id":"rs1417357176","clinical_significance":[]},{"id":"rs1237647823","seq_region_name":"7","clinical_significance":[],"end":140435148,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140435148,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1799766751","clinical_significance":[],"end":140435150,"alleles":["T","-"],"strand":1,"feature_type":"variation","start":140435150,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140435153,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435153,"clinical_significance":[],"id":"rs1585444278","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140435161,"source":"dbSNP","strand":1,"feature_type":"variation","end":140435161,"alleles":["C","A"],"seq_region_name":"7","id":"rs1214493254","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1415291155","end":140435162,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140435162,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140435165,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140435165,"source":"dbSNP","seq_region_name":"7","id":"rs931498232","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140435166,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140435166,"source":"dbSNP","seq_region_name":"7","id":"rs984666971","clinical_significance":[]},{"source":"dbSNP","start":140435171,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140435171,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799766894"},{"feature_type":"variation","strand":1,"end":140435175,"alleles":["C","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435175,"clinical_significance":[],"seq_region_name":"7","id":"rs1799766912"},{"start":140435179,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140435179,"alleles":["T","-"],"strand":1,"feature_type":"variation","id":"rs1799766932","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1209592545","clinical_significance":[],"end":140435182,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140435182,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140435183,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140435183,"id":"rs1799766967","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1170818210","seq_region_name":"7","end":140435186,"alleles":["G","C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140435186,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140435190,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140435190,"seq_region_name":"7","id":"rs1799767007","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799767023","source":"dbSNP","start":140435191,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140435191,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs373825981","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435193,"feature_type":"variation","strand":1,"end":140435193,"alleles":["G","C"]},{"end":140435194,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140435194,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130194331"},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140435200,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140435200,"source":"dbSNP","seq_region_name":"7","id":"rs538811730","clinical_significance":[]},{"alleles":["T","C"],"end":140435204,"strand":1,"feature_type":"variation","start":140435204,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1799767078","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs982155183","clinical_significance":[],"strand":1,"feature_type":"variation","end":140435208,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140435208,"source":"dbSNP"},{"start":140435209,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140435209,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799767134","clinical_significance":[]},{"start":140435211,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","G"],"end":140435211,"strand":1,"feature_type":"variation","id":"rs1799767158","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1408157705","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140435212,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140435212,"source":"dbSNP"},{"alleles":["G","T"],"end":140435213,"feature_type":"variation","strand":1,"source":"dbSNP","start":140435213,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1585444293","seq_region_name":"7"},{"clinical_significance":[],"id":"rs767538500","seq_region_name":"7","alleles":["G","T"],"end":140435216,"feature_type":"variation","strand":1,"source":"dbSNP","start":140435216,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1307877922","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140435218,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GGGCAG","G"],"end":140435223},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140435219,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140435219,"source":"dbSNP","seq_region_name":"7","id":"rs1441094482","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1035194996","feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140435220,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435220},{"strand":1,"feature_type":"variation","end":140435225,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140435225,"source":"dbSNP","id":"rs1359530527","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1321236123","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435232,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140435232},{"clinical_significance":[],"seq_region_name":"7","id":"rs1404503339","end":140435233,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140435233,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"alleles":["A","G","T"],"end":140435235,"feature_type":"variation","strand":1,"source":"dbSNP","start":140435235,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs6464772"},{"id":"rs1799767463","seq_region_name":"7","clinical_significance":[],"end":140435236,"alleles":["A","C","T"],"strand":1,"feature_type":"variation","start":140435236,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140435239,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140435239,"source":"dbSNP","id":"rs1417803266","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140435240,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140435240,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1379680867"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799767535","source":"dbSNP","start":140435244,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140435244,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799767559","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140435249,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435249},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140435250,"source":"dbSNP","strand":1,"feature_type":"variation","end":140435250,"alleles":["A","G"],"seq_region_name":"7","id":"rs1799767576","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799767609","alleles":["G","C"],"end":140435251,"feature_type":"variation","strand":1,"source":"dbSNP","start":140435251,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1040721175","end":140435255,"alleles":["G","A","C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140435255,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"end":140435259,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140435259,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585444345"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799767687","alleles":["G","A"],"end":140435261,"feature_type":"variation","strand":1,"source":"dbSNP","start":140435261,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140435263,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140435263,"source":"dbSNP","seq_region_name":"7","id":"rs1585444347","clinical_significance":[]},{"alleles":["G","C"],"end":140435267,"strand":1,"feature_type":"variation","start":140435267,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1353846954","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140435268,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140435268,"id":"rs1799767735","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140435274,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140435274,"alleles":["G","C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs756037615"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140435275,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140435275,"seq_region_name":"7","id":"rs1799767792","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799767811","alleles":["C","G"],"end":140435281,"feature_type":"variation","strand":1,"source":"dbSNP","start":140435281,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"id":"rs991394119","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140435286,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140435286,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799767864","source":"dbSNP","start":140435289,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140435289,"alleles":["G","A"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140435290,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140435290,"source":"dbSNP","seq_region_name":"7","id":"rs1799767886","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140435291,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435291,"clinical_significance":[],"seq_region_name":"7","id":"rs1799767911"},{"clinical_significance":[],"seq_region_name":"7","id":"rs900878753","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435292,"feature_type":"variation","strand":1,"end":140435292,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs1198461938","clinical_significance":[],"start":140435296,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140435296,"alleles":["G","A","T"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140435303,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140435303,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1447871548"},{"end":140435304,"alleles":["G","C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140435304,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1278942693"},{"id":"rs2130194486","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140435311,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140435311,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1585444361","seq_region_name":"7","alleles":["A","G"],"end":140435316,"feature_type":"variation","strand":1,"source":"dbSNP","start":140435316,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1286794900","source":"dbSNP","start":140435317,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140435317,"feature_type":"variation","strand":1},{"id":"rs9648837","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140435318,"source":"dbSNP","strand":1,"feature_type":"variation","end":140435318,"alleles":["G","C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585444379","feature_type":"variation","strand":1,"end":140435320,"alleles":["T","G"],"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435320},{"seq_region_name":"7","id":"rs1799768111","clinical_significance":[],"start":140435325,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","alleles":["G","A"],"end":140435325,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140435326,"alleles":["G","A"],"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435326,"clinical_significance":[],"seq_region_name":"7","id":"rs1799768132"},{"clinical_significance":[],"seq_region_name":"7","id":"rs537179295","feature_type":"variation","strand":1,"end":140435330,"alleles":["C","T"],"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435330},{"clinical_significance":[],"seq_region_name":"7","id":"rs555381609","source":"dbSNP","start":140435338,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","end":140435338,"alleles":["C","G","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs533958848","seq_region_name":"7","feature_type":"variation","strand":1,"end":140435340,"alleles":["G","T"],"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435340},{"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435342,"feature_type":"variation","strand":1,"alleles":["C","A","G","T"],"end":140435342,"clinical_significance":[],"id":"rs918883988","seq_region_name":"7"},{"start":140435344,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","alleles":["C","T"],"end":140435344,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799768249","clinical_significance":[]},{"start":140435345,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","alleles":["C","T"],"end":140435345,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1326748268","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140435346,"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140435346,"source":"dbSNP","seq_region_name":"7","id":"rs929065530","clinical_significance":[]},{"start":140435347,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","alleles":["T","G"],"end":140435347,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799768316","clinical_significance":[]},{"source":"dbSNP","start":140435350,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140435350,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1021169251"},{"seq_region_name":"7","id":"rs890199077","clinical_significance":[],"start":140435353,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","end":140435353,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"start":140435354,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","end":140435354,"alleles":["C","G"],"strand":1,"feature_type":"variation","id":"rs1174208230","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs943238813","clinical_significance":[],"start":140435355,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","end":140435355,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"end":140435361,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140435361,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","id":"rs1799768433","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs902437918","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140435364,"source":"dbSNP","strand":1,"feature_type":"variation","end":140435364,"alleles":["C","G","T"]},{"feature_type":"variation","strand":1,"end":140435366,"alleles":["CCC","CC"],"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435364,"clinical_significance":[],"seq_region_name":"7","id":"rs2130194551"},{"id":"rs189552478","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140435365,"source":"dbSNP","strand":1,"feature_type":"variation","end":140435365,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1799768605","clinical_significance":[],"end":140435368,"alleles":["G","GG"],"strand":1,"feature_type":"variation","start":140435368,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant"},{"source":"dbSNP","start":140435369,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","end":140435369,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799768625","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1475855309","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140435370,"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140435370,"source":"dbSNP"},{"start":140435371,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","alleles":["C","G"],"end":140435371,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585444425","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140435372,"source":"dbSNP","strand":1,"feature_type":"variation","end":140435372,"alleles":["G","A","C"],"seq_region_name":"7","id":"rs1034933966","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1191919390","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140435374,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435374},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799768753","consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435380,"feature_type":"variation","strand":1,"end":140435380,"alleles":["C","G"]},{"feature_type":"variation","strand":1,"end":140435383,"alleles":["C","A"],"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435383,"clinical_significance":[],"seq_region_name":"7","id":"rs1488197314"},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140435386,"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140435386,"source":"dbSNP","id":"rs1258772262","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs555685899","consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435389,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140435389},{"seq_region_name":"7","id":"rs1167276305","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140435393,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140435393},{"seq_region_name":"7","id":"rs1799768872","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140435394,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140435394},{"seq_region_name":"7","id":"rs1799768893","clinical_significance":[],"start":140435396,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","alleles":["C","T"],"end":140435396,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1486331356","feature_type":"variation","strand":1,"end":140435397,"alleles":["G","A"],"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435397},{"alleles":["C","T"],"end":140435403,"feature_type":"variation","strand":1,"source":"dbSNP","start":140435403,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1020972300"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799768957","feature_type":"variation","strand":1,"end":140435405,"alleles":["T","C"],"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435405},{"seq_region_name":"7","id":"rs1275914999","clinical_significance":[],"start":140435406,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","alleles":["C","T"],"end":140435406,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799768982","end":140435414,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140435414,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799769006","alleles":["G","C"],"end":140435420,"feature_type":"variation","strand":1,"source":"dbSNP","start":140435420,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38"},{"end":140435421,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140435421,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1218193995","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1799769043","seq_region_name":"7","source":"dbSNP","start":140435422,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","end":140435422,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130194622","feature_type":"variation","strand":1,"end":140435423,"alleles":["T","C"],"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435423},{"seq_region_name":"7","id":"rs181559279","clinical_significance":[],"alleles":["G","A","C"],"end":140435424,"strand":1,"feature_type":"variation","start":140435424,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant"},{"start":140435425,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","alleles":["G","T"],"end":140435425,"strand":1,"feature_type":"variation","id":"rs1023068302","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1310900006","source":"dbSNP","start":140435430,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140435430,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1035144106","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140435435,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140435435},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140435436,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435436,"clinical_significance":[],"seq_region_name":"7","id":"rs1799769161"},{"clinical_significance":[],"id":"rs1339625536","seq_region_name":"7","end":140435437,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140435437,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38"},{"end":140435438,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140435438,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1313335516","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799769230","source":"dbSNP","start":140435439,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140435439,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs952748546","clinical_significance":[],"end":140435441,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140435441,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant"},{"id":"rs984307243","seq_region_name":"7","clinical_significance":[],"end":140435444,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140435444,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant"},{"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435447,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140435447,"clinical_significance":[],"seq_region_name":"7","id":"rs544769000"},{"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140435450,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140435450,"seq_region_name":"7","id":"rs1333585413","clinical_significance":[]},{"end":140435452,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140435452,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1410640974"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799769341","end":140435454,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140435454,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140435456,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140435456,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799769369"},{"clinical_significance":[],"seq_region_name":"7","id":"rs563176433","source":"dbSNP","start":140435459,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140435459,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1012429483","consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435461,"feature_type":"variation","strand":1,"end":140435461,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs186024477","consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435464,"feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140435464},{"source":"dbSNP","start":140435466,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140435466,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130194670"},{"seq_region_name":"7","id":"rs1799769467","clinical_significance":[],"start":140435467,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","end":140435467,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435468,"feature_type":"variation","strand":1,"end":140435468,"alleles":["G","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1168825477"},{"alleles":["T","C"],"end":140435469,"strand":1,"feature_type":"variation","start":140435469,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","id":"rs1328295494","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","T"],"end":140435470,"strand":1,"feature_type":"variation","start":140435470,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","seq_region_name":"7","id":"rs1428796235","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799769554","clinical_significance":[],"alleles":["CCC","CC"],"end":140435472,"strand":1,"feature_type":"variation","start":140435470,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant"},{"seq_region_name":"7","id":"rs961557998","clinical_significance":[],"alleles":["C","T"],"end":140435472,"strand":1,"feature_type":"variation","start":140435472,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant"},{"seq_region_name":"7","id":"rs1269672789","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140435473,"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140435473,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140435473,"source":"dbSNP","strand":1,"feature_type":"variation","end":140435476,"alleles":["GGGG","GGG"],"seq_region_name":"7","id":"rs1419042939","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799769637","source":"dbSNP","start":140435474,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140435474,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140435475,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140435475,"seq_region_name":"7","id":"rs977446108","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs922837270","end":140435476,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140435476,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799769691","consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435478,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140435478},{"end":140435479,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140435479,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","seq_region_name":"7","id":"rs79284543","clinical_significance":[]},{"clinical_significance":[],"id":"rs1208785423","seq_region_name":"7","source":"dbSNP","start":140435481,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","end":140435481,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799769770","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140435487,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435487},{"id":"rs369043304","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140435490,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140435490},{"seq_region_name":"7","id":"rs1274622524","clinical_significance":[],"end":140435491,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140435491,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant"},{"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140435493,"source":"dbSNP","strand":1,"feature_type":"variation","end":140435493,"alleles":["A","G"],"seq_region_name":"7","id":"rs1196367178","clinical_significance":[]},{"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435496,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140435496,"clinical_significance":[],"seq_region_name":"7","id":"rs1317009829"},{"id":"rs560935245","seq_region_name":"7","clinical_significance":[],"start":140435499,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","end":140435499,"alleles":["C","A","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1293665250","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140435501,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140435501},{"seq_region_name":"7","id":"rs1799769887","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140435504,"source":"dbSNP","strand":1,"feature_type":"variation","end":140435504,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1799769911","clinical_significance":[],"alleles":["GGG","GG"],"end":140435511,"strand":1,"feature_type":"variation","start":140435509,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant"},{"seq_region_name":"7","id":"rs1234978746","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140435510,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140435510},{"alleles":["G","A"],"end":140435511,"feature_type":"variation","strand":1,"source":"dbSNP","start":140435511,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs973360485"},{"start":140435513,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","alleles":["A","G","T"],"end":140435513,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1283577357","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140435518,"source":"dbSNP","strand":1,"feature_type":"variation","end":140435518,"alleles":["G","C"],"seq_region_name":"7","id":"rs1799770015","clinical_significance":[]},{"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435519,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140435519,"clinical_significance":[],"id":"rs1799770041","seq_region_name":"7"},{"id":"rs1799770066","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140435522,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TCCCCCGCGG","-"],"end":140435531},{"clinical_significance":[],"id":"rs1356385178","seq_region_name":"7","source":"dbSNP","start":140435523,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140435523,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1442961653","clinical_significance":[],"start":140435523,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","end":140435527,"alleles":["CCCCC","-"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs914996492","clinical_significance":[],"start":140435525,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","end":140435525,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs950423750","clinical_significance":[],"end":140435527,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140435527,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant"},{"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140435527,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CGCGGG","CGCGGGACCTCGCGGG"],"end":140435532,"seq_region_name":"7","id":"rs1799770165","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs562649444","consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435527,"feature_type":"variation","strand":1,"end":140435551,"alleles":["CGCGGGCCCTCGCGGGCCCTCGCGG","CGCGGGCCCTCGCGG","CGCGGGCCCTCGCGGGCCCTCGCGGGCCCTCGCGG"]},{"seq_region_name":"7","id":"rs1422481656","clinical_significance":[],"strand":1,"feature_type":"variation","end":140435528,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140435528,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799770265","feature_type":"variation","strand":1,"end":140435529,"alleles":["C","T"],"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435529},{"strand":1,"feature_type":"variation","end":140435530,"alleles":["G","C","T"],"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140435530,"source":"dbSNP","seq_region_name":"7","id":"rs946425795","clinical_significance":[]},{"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435531,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140435531,"clinical_significance":[],"seq_region_name":"7","id":"rs2130194819"},{"alleles":["G","A","C","T"],"end":140435532,"strand":1,"feature_type":"variation","start":140435532,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","seq_region_name":"7","id":"rs1799770307","clinical_significance":[]},{"seq_region_name":"7","id":"rs1178311554","clinical_significance":[],"start":140435533,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","alleles":["C","T"],"end":140435533,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130194832","source":"dbSNP","start":140435536,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","end":140435536,"alleles":["T","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1263329958","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140435537,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435537},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140435538,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435538,"clinical_significance":[],"id":"rs1444909287","seq_region_name":"7"},{"end":140435540,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140435540,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","id":"rs1799770385","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140435541,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140435541,"source":"dbSNP","seq_region_name":"7","id":"rs1042133096","clinical_significance":[]},{"id":"rs1799770431","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140435542,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140435542,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140435543,"alleles":["C","G"],"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435543,"clinical_significance":[],"seq_region_name":"7","id":"rs2130194855"},{"seq_region_name":"7","id":"rs1799770451","clinical_significance":[],"start":140435544,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","end":140435544,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"alleles":["T","C","G"],"end":140435546,"strand":1,"feature_type":"variation","start":140435546,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","seq_region_name":"7","id":"rs1176303605","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130194869","feature_type":"variation","strand":1,"end":140435547,"alleles":["C","G"],"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435547},{"strand":1,"feature_type":"variation","end":140435548,"alleles":["G","GG"],"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140435548,"source":"dbSNP","seq_region_name":"7","id":"rs1457037928","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799770498","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140435548,"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140435548,"source":"dbSNP"},{"alleles":["C","G","T"],"end":140435549,"feature_type":"variation","strand":1,"source":"dbSNP","start":140435549,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1273469991"},{"seq_region_name":"7","id":"rs1799770549","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140435550,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140435550},{"alleles":["G","C"],"end":140435551,"feature_type":"variation","strand":1,"source":"dbSNP","start":140435551,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs911669939","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140435555,"source":"dbSNP","strand":1,"feature_type":"variation","end":140435555,"alleles":["C","T"],"id":"rs1799770589","seq_region_name":"7","clinical_significance":[]},{"end":140435556,"alleles":["C","A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140435556,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1319729926"},{"alleles":["G","A","C","T"],"end":140435557,"strand":1,"feature_type":"variation","start":140435557,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","seq_region_name":"7","id":"rs761630892","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140435557,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GG","G"],"end":140435558,"seq_region_name":"7","id":"rs1799770660","clinical_significance":[]},{"end":140435558,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140435558,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1224277690"},{"seq_region_name":"7","id":"rs1799770706","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140435561,"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140435561,"source":"dbSNP"},{"seq_region_name":"7","id":"rs528439144","clinical_significance":[],"alleles":["G","C"],"end":140435562,"strand":1,"feature_type":"variation","start":140435562,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant"},{"seq_region_name":"7","id":"rs1799770751","clinical_significance":[],"strand":1,"feature_type":"variation","end":140435565,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140435565,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1307165872","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140435566,"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140435566,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1371964222","source":"dbSNP","start":140435567,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","end":140435567,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1446223885","clinical_significance":[],"start":140435568,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","end":140435567,"alleles":["-","A"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140435568,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435568,"clinical_significance":[],"seq_region_name":"7","id":"rs1328197722"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1456673715","feature_type":"variation","strand":1,"end":140435578,"alleles":["CTGTGCGCCT","-"],"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435569},{"clinical_significance":[],"seq_region_name":"7","id":"rs1349665476","source":"dbSNP","start":140435570,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","end":140435570,"alleles":["T","A","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799770910","source":"dbSNP","start":140435574,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","end":140435574,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1003359778","clinical_significance":[],"strand":1,"feature_type":"variation","end":140435575,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140435575,"source":"dbSNP"},{"start":140435575,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","alleles":["GCCTGCGTCCTTCCCCACCAGC","GC"],"end":140435596,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1171639209","clinical_significance":[]},{"alleles":["T","C"],"end":140435578,"feature_type":"variation","strand":1,"source":"dbSNP","start":140435578,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799770970"},{"id":"rs540627734","seq_region_name":"7","clinical_significance":[],"start":140435579,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","alleles":["G","T"],"end":140435579,"strand":1,"feature_type":"variation"},{"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435580,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140435580,"clinical_significance":[],"seq_region_name":"7","id":"rs1799771014"},{"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435581,"feature_type":"variation","strand":1,"end":140435581,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs915021573"},{"start":140435582,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","end":140435586,"alleles":["TCCTT","-"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799771055","clinical_significance":[]},{"source":"dbSNP","start":140435584,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140435584,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1176198879"},{"seq_region_name":"7","id":"rs1160226461","clinical_significance":[],"alleles":["TCC","TCCTCC"],"end":140435588,"strand":1,"feature_type":"variation","start":140435586,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant"},{"end":140435589,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140435589,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799771126","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs895034549","consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435594,"feature_type":"variation","strand":1,"end":140435594,"alleles":["A","G"]},{"id":"rs1387505162","seq_region_name":"7","clinical_significance":[],"start":140435597,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","alleles":["G","A"],"end":140435597,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140435602,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140435602,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799771198"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799771219","consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435603,"feature_type":"variation","strand":1,"end":140435603,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130194985","consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435605,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140435605},{"start":140435607,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","alleles":["C","G","T"],"end":140435607,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799771250","clinical_significance":[]},{"end":140435619,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","start":140435619,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","seq_region_name":"7","id":"rs372424524","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799771317","seq_region_name":"7","feature_type":"variation","strand":1,"end":140435620,"alleles":["TG","-"],"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435619},{"clinical_significance":[],"seq_region_name":"7","id":"rs1012940023","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140435621,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435621},{"id":"rs1245926005","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140435623,"source":"dbSNP","strand":1,"feature_type":"variation","end":140435623,"alleles":["T","A"]},{"id":"rs1022932348","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140435624,"source":"dbSNP","strand":1,"feature_type":"variation","end":140435624,"alleles":["C","A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1317780008","source":"dbSNP","start":140435626,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140435626,"feature_type":"variation","strand":1},{"start":140435628,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","end":140435628,"alleles":["T","TT"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1331701309","clinical_significance":[]},{"end":140435628,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140435628,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1585444648","seq_region_name":"7"},{"start":140435633,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","end":140435633,"alleles":["C","A","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1443789438","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140435635,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","G","T"],"end":140435635,"id":"rs4385389","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799771597","clinical_significance":[],"strand":1,"feature_type":"variation","end":140435636,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140435636,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs369334097","consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435638,"feature_type":"variation","strand":1,"end":140435638,"alleles":["G","A"]},{"source":"dbSNP","start":140435641,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140435641,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799771640"},{"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140435644,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140435644,"id":"rs750070821","seq_region_name":"7","clinical_significance":[]},{"end":140435646,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140435646,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","id":"rs1370732730","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs139095053","source":"dbSNP","start":140435649,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","end":140435649,"alleles":["G","A"],"feature_type":"variation","strand":1},{"alleles":["C","A"],"end":140435653,"strand":1,"feature_type":"variation","start":140435653,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","id":"rs1799771740","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799771763","consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435655,"feature_type":"variation","strand":1,"end":140435655,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799771789","consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435659,"feature_type":"variation","strand":1,"end":140435659,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1015673988","end":140435660,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140435660,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1433379524","clinical_significance":[],"start":140435662,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","alleles":["T","G"],"end":140435662,"strand":1,"feature_type":"variation"},{"end":140435663,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140435663,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","seq_region_name":"7","id":"rs2130195059","clinical_significance":[]},{"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435665,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140435665,"clinical_significance":[],"seq_region_name":"7","id":"rs1799771847"},{"end":140435666,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140435666,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1359161489","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140435668,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140435668,"seq_region_name":"7","id":"rs551181395","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130195070","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140435671,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140435671},{"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435672,"feature_type":"variation","strand":1,"end":140435672,"alleles":["G","A","C"],"clinical_significance":[],"id":"rs2363824","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140435674,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140435674,"source":"dbSNP","id":"rs1056466550","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140435675,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","end":140435675,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs530618483"},{"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435678,"feature_type":"variation","strand":1,"end":140435678,"alleles":["C","A","T"],"clinical_significance":[],"id":"rs1348147245","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799772064","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140435679,"source":"dbSNP","strand":1,"feature_type":"variation","end":140435679,"alleles":["C","G"]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140435680,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435680,"clinical_significance":[],"seq_region_name":"7","id":"rs1799772086"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1186860956","consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435688,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140435688},{"seq_region_name":"7","id":"rs1204137697","clinical_significance":[],"end":140435694,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140435694,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant"},{"start":140435696,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","alleles":["G","A"],"end":140435696,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs374058083","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799772171","seq_region_name":"7","source":"dbSNP","start":140435697,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140435697,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1012705059","consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435699,"feature_type":"variation","strand":1,"end":140435701,"alleles":["CCC","CC"]},{"end":140435700,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140435700,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs765905819"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1486004855","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140435701,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435701},{"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140435702,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140435702,"seq_region_name":"7","id":"rs1257816680","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140435703,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140435703,"source":"dbSNP","seq_region_name":"7","id":"rs1799772275","clinical_significance":[]},{"id":"rs1231241306","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140435706,"source":"dbSNP","strand":1,"feature_type":"variation","end":140435706,"alleles":["G","T"]},{"seq_region_name":"7","id":"rs562967709","clinical_significance":[],"strand":1,"feature_type":"variation","end":140435710,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140435710,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1296620918","end":140435712,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140435712,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1220792228","seq_region_name":"7","source":"dbSNP","start":140435715,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140435715,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140435716,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140435716,"seq_region_name":"7","id":"rs1338946098","clinical_significance":[]},{"id":"rs2130195170","seq_region_name":"7","clinical_significance":[],"alleles":["C","A"],"end":140435717,"strand":1,"feature_type":"variation","start":140435717,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant"},{"seq_region_name":"7","id":"rs1191683308","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140435719,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140435719},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140435720,"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140435720,"source":"dbSNP","seq_region_name":"7","id":"rs994291244","clinical_significance":[]},{"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435721,"feature_type":"variation","strand":1,"end":140435721,"alleles":["A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799772543"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799772556","end":140435722,"alleles":["AA","AAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140435721,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38"},{"end":140435724,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140435724,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1304078763","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1252366348","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140435731,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140435731},{"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140435732,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140435732,"seq_region_name":"7","id":"rs1799772618","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs954257735","alleles":["G","C"],"end":140435733,"feature_type":"variation","strand":1,"source":"dbSNP","start":140435733,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140435735,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140435735,"seq_region_name":"7","id":"rs1799772647","clinical_significance":[]},{"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435741,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140435741,"clinical_significance":[],"seq_region_name":"7","id":"rs1799772670"},{"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435743,"feature_type":"variation","strand":1,"end":140435743,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799772691"},{"end":140435764,"alleles":["CCGCAGCGAAACCCGCAGCG","CCGCAGCG"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140435745,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1440237217"},{"clinical_significance":[],"id":"rs1170740457","seq_region_name":"7","end":140435766,"alleles":["CGCAGCGAAACCCGCAGCGCA","CGCAGCGAAACCCGCAGCGCACGCAGCGAAACCCGCAGCGCA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140435746,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["G","C","T"],"end":140435747,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435747,"clinical_significance":[],"seq_region_name":"7","id":"rs1799772851"},{"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140435748,"source":"dbSNP","strand":1,"feature_type":"variation","end":140435748,"alleles":["C","T"],"seq_region_name":"7","id":"rs2130195218","clinical_significance":[]},{"seq_region_name":"7","id":"rs1183776581","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","G"],"end":140435751,"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140435751,"source":"dbSNP"},{"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435757,"feature_type":"variation","strand":1,"end":140435757,"alleles":["C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799772899"},{"clinical_significance":[],"id":"rs1585444728","seq_region_name":"7","alleles":["C","G","T"],"end":140435758,"feature_type":"variation","strand":1,"source":"dbSNP","start":140435758,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1025873530","clinical_significance":[],"alleles":["A","C"],"end":140435761,"strand":1,"feature_type":"variation","start":140435761,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant"},{"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435763,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140435763,"clinical_significance":[],"seq_region_name":"7","id":"rs1799772961"},{"alleles":["C","A","G","T"],"end":140435768,"feature_type":"variation","strand":1,"source":"dbSNP","start":140435768,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1192738376"},{"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140435769,"source":"dbSNP","strand":1,"feature_type":"variation","end":140435769,"alleles":["G","A"],"seq_region_name":"7","id":"rs1361829370","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799773044","consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435770,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140435770},{"seq_region_name":"7","id":"rs985101269","clinical_significance":[],"strand":1,"feature_type":"variation","end":140435774,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140435774,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799773097","clinical_significance":[],"end":140435776,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140435776,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs751032917","end":140435778,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140435778,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38"},{"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435779,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140435779,"clinical_significance":[],"seq_region_name":"7","id":"rs2130195257"},{"alleles":["G","A"],"end":140435781,"strand":1,"feature_type":"variation","start":140435781,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","seq_region_name":"7","id":"rs1799773140","clinical_significance":[]},{"end":140435782,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140435782,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1158165690","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140435783,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140435783,"seq_region_name":"7","id":"rs567356770","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140435784,"alleles":["G","-"],"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435784,"clinical_significance":[],"seq_region_name":"7","id":"rs2130195270"},{"seq_region_name":"7","id":"rs1042555444","clinical_significance":[],"start":140435786,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","end":140435786,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs911536082","clinical_significance":[],"start":140435792,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","alleles":["C","A","G","T"],"end":140435792,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140435792,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","alleles":["CGCCCGGTCCGCGGGCCGCC","CGCC"],"end":140435811,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1395313896"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1316389126","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140435793,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435793},{"clinical_significance":[],"seq_region_name":"7","id":"rs1277947977","feature_type":"variation","strand":1,"end":140435794,"alleles":["C","T"],"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435794},{"end":140435796,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140435796,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","id":"rs1799773305","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435797,"feature_type":"variation","strand":1,"end":140435797,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs755480509"},{"seq_region_name":"7","id":"rs1799773345","clinical_significance":[],"strand":1,"feature_type":"variation","end":140435800,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140435800,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140435801,"alleles":["CC","C"],"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435800,"clinical_significance":[],"seq_region_name":"7","id":"rs964497009"},{"clinical_significance":[],"seq_region_name":"7","id":"rs149481931","feature_type":"variation","strand":1,"end":140435802,"alleles":["G","A"],"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435802},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140435804,"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140435804,"source":"dbSNP","seq_region_name":"7","id":"rs1799773436","clinical_significance":[]},{"clinical_significance":[],"id":"rs2130195319","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140435806,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435806},{"strand":1,"feature_type":"variation","end":140435808,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140435808,"source":"dbSNP","seq_region_name":"7","id":"rs1311272645","clinical_significance":[]},{"alleles":["G","T"],"end":140435809,"feature_type":"variation","strand":1,"source":"dbSNP","start":140435809,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs914989601"},{"id":"rs545569216","seq_region_name":"7","clinical_significance":[],"alleles":["C","G","T"],"end":140435811,"strand":1,"feature_type":"variation","start":140435811,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant"},{"seq_region_name":"7","id":"rs1799773547","clinical_significance":[],"start":140435815,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","end":140435815,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs571433846","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435819,"feature_type":"variation","strand":1,"end":140435819,"alleles":["C","A","T"]},{"seq_region_name":"7","id":"rs1466848673","clinical_significance":[],"start":140435823,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140435823,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1397752311","feature_type":"variation","strand":1,"end":140435824,"alleles":["T","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435824},{"alleles":["A","G"],"end":140435829,"strand":1,"feature_type":"variation","start":140435829,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1169655913","clinical_significance":[]},{"clinical_significance":[],"id":"rs1461811806","seq_region_name":"7","feature_type":"variation","strand":1,"end":140435832,"alleles":["T","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435832},{"clinical_significance":[],"seq_region_name":"7","id":"rs560189197","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435833,"feature_type":"variation","strand":1,"end":140435833,"alleles":["A","T"]},{"alleles":["A","G"],"end":140435834,"feature_type":"variation","strand":1,"source":"dbSNP","start":140435834,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs377410993"},{"seq_region_name":"7","id":"rs1799773724","clinical_significance":[],"end":140435835,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140435835,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"end":140435838,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140435838,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs61023017"},{"feature_type":"variation","strand":1,"alleles":["ACAACA","ACA"],"end":140435844,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435839,"clinical_significance":[],"seq_region_name":"7","id":"rs1799773811"},{"start":140435843,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140435843,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1423252972","clinical_significance":[]},{"alleles":["A","G"],"end":140435847,"strand":1,"feature_type":"variation","start":140435847,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1284366355","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799773886","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435849,"feature_type":"variation","strand":1,"end":140435849,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs368276956","source":"dbSNP","start":140435851,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140435851,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1799773928","clinical_significance":[],"alleles":["A","T"],"end":140435852,"strand":1,"feature_type":"variation","start":140435852,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs939225348","clinical_significance":[],"strand":1,"feature_type":"variation","end":140435853,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140435853,"source":"dbSNP"},{"start":140435860,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140435860,"alleles":["T","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1336481448","clinical_significance":[]},{"seq_region_name":"7","id":"rs1048999174","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140435861,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140435861},{"start":140435870,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140435870,"alleles":["A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799774020","clinical_significance":[]},{"start":140435872,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","A"],"end":140435872,"strand":1,"feature_type":"variation","id":"rs1799774043","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140435877,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140435877,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs778058534"},{"end":140435902,"alleles":["CTGTAGTCCCATTTCTCGCAGGCTCG","-"],"strand":1,"feature_type":"variation","start":140435877,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799774085","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140435882,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435882,"clinical_significance":[],"seq_region_name":"7","id":"rs1799774106"},{"clinical_significance":[],"id":"rs1056479857","seq_region_name":"7","source":"dbSNP","start":140435885,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140435885,"alleles":["C","A","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs895104970","clinical_significance":[],"strand":1,"feature_type":"variation","end":140435886,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140435886,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1264165481","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435889,"feature_type":"variation","strand":1,"end":140435889,"alleles":["T","C"]},{"clinical_significance":[],"id":"rs143984096","seq_region_name":"7","feature_type":"variation","strand":1,"end":140435890,"alleles":["T","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435890},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435893,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140435893,"clinical_significance":[],"seq_region_name":"7","id":"rs1336928694"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140435899,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435899,"clinical_significance":[],"seq_region_name":"7","id":"rs1585444836"},{"source":"dbSNP","start":140435901,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140435901,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799774260"},{"end":140435902,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140435902,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs527959685"},{"id":"rs1799774327","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140435914,"strand":1,"feature_type":"variation","start":140435914,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140435918,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140435918,"source":"dbSNP","seq_region_name":"7","id":"rs1005531187","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs898559388","end":140435920,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140435920,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"end":140435922,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140435922,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1387094027","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799774408","end":140435926,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140435926,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1799774426","clinical_significance":[],"start":140435929,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140435929,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1392621007","source":"dbSNP","start":140435933,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140435933,"alleles":["T","C"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140435938,"source":"dbSNP","strand":1,"feature_type":"variation","end":140435938,"alleles":["G","A"],"seq_region_name":"7","id":"rs575134895","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435939,"feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140435939,"clinical_significance":[],"seq_region_name":"7","id":"rs1585444853"},{"seq_region_name":"7","id":"rs544330165","clinical_significance":[],"end":140435952,"alleles":["TGTGTGTGTG","TGTGTGTGTGTG"],"strand":1,"feature_type":"variation","start":140435943,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1418217790","source":"dbSNP","start":140435947,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140435947,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140435948,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["GTGTGCGTGTG","GTGTGCGTGTGCGTGTG"],"end":140435958,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs994322525"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1364380014","feature_type":"variation","strand":1,"alleles":["GCG","GCGCG"],"end":140435954,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435952},{"start":140435953,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140435953,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1563079222","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs891397948","alleles":["G","A","C"],"end":140435954,"feature_type":"variation","strand":1,"source":"dbSNP","start":140435954,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1025737507","seq_region_name":"7","feature_type":"variation","strand":1,"end":140435965,"alleles":["GTGTGTGTGTGT","GTGTGTGTGT","GTGTGTGTGTGTGT"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435954},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799774694","source":"dbSNP","start":140435955,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140435955,"alleles":["T","C"],"feature_type":"variation","strand":1},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435956,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140435956,"clinical_significance":[],"seq_region_name":"7","id":"rs1181374959"},{"source":"dbSNP","start":140435958,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140435958,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs376270583"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1016120072","source":"dbSNP","start":140435962,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140435962,"alleles":["G","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1265688697","clinical_significance":[],"start":140435965,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140435965,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1418920926","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140435966,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140435966},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799774820","feature_type":"variation","strand":1,"end":140435974,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435974},{"start":140435975,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140435975,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799774841","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799774859","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435978,"feature_type":"variation","strand":1,"end":140435978,"alleles":["A","T"]},{"end":140435980,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140435980,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs897207296","seq_region_name":"7"},{"clinical_significance":[],"id":"rs749522612","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140435982,"feature_type":"variation","strand":1,"end":140435982,"alleles":["C","G"]},{"start":140435983,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","T"],"end":140435983,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1351984310","clinical_significance":[]},{"source":"dbSNP","start":140435985,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140435985,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799774938"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799774959","alleles":["C","A","T"],"end":140435986,"feature_type":"variation","strand":1,"source":"dbSNP","start":140435986,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140435987,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140435987,"source":"dbSNP","seq_region_name":"7","id":"rs964768205","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140435988,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140435988,"source":"dbSNP","seq_region_name":"7","id":"rs998313525","clinical_significance":[]},{"alleles":["C","A"],"end":140436000,"feature_type":"variation","strand":1,"source":"dbSNP","start":140436000,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799775036"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799775056","source":"dbSNP","start":140436002,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140436002,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1799775075","clinical_significance":[],"alleles":["A","AA"],"end":140436002,"strand":1,"feature_type":"variation","start":140436002,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1799775101","clinical_significance":[],"alleles":["C","T"],"end":140436008,"strand":1,"feature_type":"variation","start":140436008,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"end":140436009,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140436009,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1307990547","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1462973840","feature_type":"variation","strand":1,"end":140436013,"alleles":["T","A","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436013},{"clinical_significance":[],"id":"rs1799775172","seq_region_name":"7","source":"dbSNP","start":140436014,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140436014,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1799775192","clinical_significance":[],"start":140436017,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140436017,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799775219","source":"dbSNP","start":140436020,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140436020,"alleles":["G","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs542426259","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436022,"source":"dbSNP","strand":1,"feature_type":"variation","end":140436022,"alleles":["C","T"]},{"alleles":["G","A"],"end":140436024,"feature_type":"variation","strand":1,"source":"dbSNP","start":140436024,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs967778075"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140436026,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436026,"clinical_significance":[],"seq_region_name":"7","id":"rs1585444915"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436027,"feature_type":"variation","strand":1,"end":140436027,"alleles":["G","A"],"clinical_significance":[],"id":"rs1321334627","seq_region_name":"7"},{"end":140436028,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140436028,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1386046979","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436029,"feature_type":"variation","strand":1,"end":140436029,"alleles":["G","A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs114390609"},{"start":140436030,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A","C"],"end":140436030,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1299992059","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799775383","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436030,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GGAGGA","GGA"],"end":140436035},{"id":"rs1585444932","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436031,"source":"dbSNP","strand":1,"feature_type":"variation","end":140436031,"alleles":["G","C"]},{"strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140436032,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436032,"source":"dbSNP","seq_region_name":"7","id":"rs1417899857","clinical_significance":[]},{"seq_region_name":"7","id":"rs1379773998","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436033,"source":"dbSNP","strand":1,"feature_type":"variation","end":140436033,"alleles":["G","A","C"]},{"seq_region_name":"7","id":"rs1799775486","clinical_significance":[],"end":140436033,"alleles":["-","CTCCC"],"strand":1,"feature_type":"variation","start":140436034,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"id":"rs923729784","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436037,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140436037},{"seq_region_name":"7","id":"rs985716914","clinical_significance":[],"alleles":["G","A"],"end":140436038,"strand":1,"feature_type":"variation","start":140436038,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1313869763","clinical_significance":[],"start":140436039,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140436039,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"start":140436042,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140436042,"alleles":["G","C","T"],"strand":1,"feature_type":"variation","id":"rs939256398","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1447959363","clinical_significance":[],"start":140436045,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140436045,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140436047,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436047,"clinical_significance":[],"id":"rs992110763","seq_region_name":"7"},{"start":140436048,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","T"],"end":140436048,"strand":1,"feature_type":"variation","id":"rs1799775652","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436050,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140436050,"seq_region_name":"7","id":"rs916498357","clinical_significance":[]},{"clinical_significance":[],"id":"rs1231054489","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140436052,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436052},{"strand":1,"feature_type":"variation","end":140436057,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436057,"source":"dbSNP","seq_region_name":"7","id":"rs1799775712","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140436059,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436059,"clinical_significance":[],"id":"rs1215089167","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799775751","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436062,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140436062},{"clinical_significance":[],"seq_region_name":"7","id":"rs1486988599","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436066,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140436066},{"seq_region_name":"7","id":"rs1284671507","clinical_significance":[],"alleles":["C","A","G"],"end":140436075,"strand":1,"feature_type":"variation","start":140436075,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1799775822","clinical_significance":[],"start":140436081,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140436081,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140436083,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436083,"clinical_significance":[],"seq_region_name":"7","id":"rs190746226"},{"clinical_significance":[],"id":"rs1799775862","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","A"],"end":140436085,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436085},{"seq_region_name":"7","id":"rs1799775881","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436088,"source":"dbSNP","strand":1,"feature_type":"variation","end":140436088,"alleles":["A","G"]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436090,"source":"dbSNP","strand":1,"feature_type":"variation","end":140436093,"alleles":["AAAA","AA"],"id":"rs1038357069","seq_region_name":"7","clinical_significance":[]},{"start":140436095,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["TTTTTTT","TTTTTT"],"end":140436101,"strand":1,"feature_type":"variation","id":"rs1799775958","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799775971","feature_type":"variation","strand":1,"end":140436103,"alleles":["A","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436103},{"alleles":["T","C"],"end":140436105,"feature_type":"variation","strand":1,"source":"dbSNP","start":140436105,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799775991"},{"seq_region_name":"7","id":"rs28412759","clinical_significance":[],"alleles":["T","C"],"end":140436108,"strand":1,"feature_type":"variation","start":140436108,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs977757775","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436113,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140436113},{"source":"dbSNP","start":140436117,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140436117,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1232200443"},{"id":"rs1340934436","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140436118,"alleles":["T","C","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436118,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436119,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140436119,"seq_region_name":"7","id":"rs74805855","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140436120,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436120,"source":"dbSNP","id":"rs939075781","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140436129,"alleles":["T","A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436129,"clinical_significance":[],"id":"rs1378666953","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs991999714","source":"dbSNP","start":140436137,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140436137,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1799776227","seq_region_name":"7","alleles":["C","T"],"end":140436140,"feature_type":"variation","strand":1,"source":"dbSNP","start":140436140,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1799776245","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436147,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140436147},{"seq_region_name":"7","id":"rs1799776269","clinical_significance":[],"strand":1,"feature_type":"variation","end":140436155,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436155,"source":"dbSNP"},{"start":140436157,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140436157,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1359894839","clinical_significance":[]},{"seq_region_name":"7","id":"rs891262157","clinical_significance":[],"start":140436158,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","A"],"end":140436158,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1416287773","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140436160,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436160,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799776344","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436161,"feature_type":"variation","strand":1,"end":140436161,"alleles":["G","A"]},{"id":"rs1799776360","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436166,"source":"dbSNP","strand":1,"feature_type":"variation","end":140436166,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1008345751","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436167,"source":"dbSNP","strand":1,"feature_type":"variation","end":140436167,"alleles":["C","G"]},{"alleles":["T","A"],"end":140436171,"strand":1,"feature_type":"variation","start":140436171,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1563079273","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140436174,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436174,"source":"dbSNP","id":"rs2130195899","seq_region_name":"7","clinical_significance":[]},{"end":140436176,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140436176,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs745972908","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436177,"feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140436177,"clinical_significance":[],"seq_region_name":"7","id":"rs1172243231"},{"seq_region_name":"7","id":"rs1018983562","clinical_significance":[],"strand":1,"feature_type":"variation","end":140436181,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436181,"source":"dbSNP"},{"id":"rs1799776481","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436184,"source":"dbSNP","strand":1,"feature_type":"variation","end":140436184,"alleles":["C","T"]},{"start":140436185,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140436185,"strand":1,"feature_type":"variation","id":"rs900064617","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs996275295","alleles":["T","C"],"end":140436190,"feature_type":"variation","strand":1,"source":"dbSNP","start":140436190,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1417258462","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436195,"feature_type":"variation","strand":1,"alleles":["GTG","G"],"end":140436197},{"start":140436196,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140436196,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs1429138394","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","T"],"end":140436198,"feature_type":"variation","strand":1,"source":"dbSNP","start":140436198,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1210183234"},{"end":140436199,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140436199,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs55961611","seq_region_name":"7"},{"clinical_significance":[],"id":"rs967792563","seq_region_name":"7","feature_type":"variation","strand":1,"end":140436206,"alleles":["T","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436206},{"alleles":["C","A"],"end":140436213,"feature_type":"variation","strand":1,"source":"dbSNP","start":140436213,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799776717"},{"id":"rs1049029395","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140436214,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436214,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436217,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140436217,"seq_region_name":"7","id":"rs977801556","clinical_significance":[]},{"seq_region_name":"7","id":"rs887685248","clinical_significance":[],"start":140436218,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140436218,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436220,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140436220,"seq_region_name":"7","id":"rs1799776782","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs941369301","feature_type":"variation","strand":1,"end":140436221,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436221},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436224,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140436224,"seq_region_name":"7","id":"rs1799776816","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1371922585","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436229,"feature_type":"variation","strand":1,"end":140436229,"alleles":["G","A"]},{"id":"rs1799776856","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436235,"source":"dbSNP","strand":1,"feature_type":"variation","end":140436235,"alleles":["G","A"]},{"id":"rs1318265724","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436236,"source":"dbSNP","strand":1,"feature_type":"variation","end":140436236,"alleles":["A","G"]},{"end":140436238,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140436238,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1279849893","clinical_significance":[]},{"start":140436244,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140436244,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs1030748406","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1036997564","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436245,"feature_type":"variation","strand":1,"end":140436245,"alleles":["C","G","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1284729011","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436247,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140436247},{"source":"dbSNP","start":140436251,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["TAAATAAATAAATAAATAAATAAA","TAAATAAATAAATAAATAAA","TAAATAAATAAATAAATAAATAAATAAA","TAAATAAATAAATAAATAAATAAATAAATAAA"],"end":140436274,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs201910969"},{"end":140436254,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140436254,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1466325525"},{"clinical_significance":[],"id":"rs1461896223","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436256,"feature_type":"variation","strand":1,"end":140436258,"alleles":["AAA","AAAA"]},{"start":140436261,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140436261,"alleles":["A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799777079","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436266,"source":"dbSNP","strand":1,"feature_type":"variation","end":140436266,"alleles":["A","G"],"id":"rs1799777101","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1174713453","feature_type":"variation","strand":1,"alleles":["T","A"],"end":140436267,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436267},{"alleles":["AAATAAAAATAAA","AAATAAA"],"end":140436280,"feature_type":"variation","strand":1,"source":"dbSNP","start":140436268,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799777145"},{"end":140436269,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","start":140436269,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs544968174","clinical_significance":[]},{"end":140436270,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140436270,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799777197","clinical_significance":[]},{"alleles":["T","A"],"end":140436271,"strand":1,"feature_type":"variation","start":140436271,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1377604711","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1184147117","seq_region_name":"7","source":"dbSNP","start":140436273,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140436273,"alleles":["A","T"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140436274,"alleles":["AA","AATTAA"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436273,"source":"dbSNP","seq_region_name":"7","id":"rs1799777256","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436274,"feature_type":"variation","strand":1,"end":140436283,"alleles":["AAATAAATAA","AAATAA","AAATAAATAAATAA"],"clinical_significance":[],"seq_region_name":"7","id":"rs1415098257"},{"id":"rs563063825","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140436275,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436275,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140436277,"alleles":["T","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436277,"clinical_significance":[],"seq_region_name":"7","id":"rs530270271"},{"end":140436281,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140436281,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs181669843","seq_region_name":"7"},{"alleles":["T","C"],"end":140436289,"strand":1,"feature_type":"variation","start":140436289,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1457906495","clinical_significance":[]},{"start":140436293,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","C"],"end":140436293,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799777406","clinical_significance":[]},{"seq_region_name":"7","id":"rs1259642146","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436294,"source":"dbSNP","strand":1,"feature_type":"variation","end":140436294,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1383470385","clinical_significance":[],"start":140436297,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A","C"],"end":140436297,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140436298,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436298,"source":"dbSNP","seq_region_name":"7","id":"rs1196470811","clinical_significance":[]},{"source":"dbSNP","start":140436300,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140436300,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799777501"},{"strand":1,"feature_type":"variation","end":140436304,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436304,"source":"dbSNP","seq_region_name":"7","id":"rs1799777522","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140436305,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436305,"source":"dbSNP","seq_region_name":"7","id":"rs1799777543","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["GCTCAACTAGGTTGCTCAA","GCTCAA"],"end":140436325,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436307,"clinical_significance":[],"seq_region_name":"7","id":"rs1799777564"},{"clinical_significance":[],"id":"rs1799777585","seq_region_name":"7","feature_type":"variation","strand":1,"end":140436317,"alleles":["G","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436317},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130196087","end":140436325,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140436325,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1799777612","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436326,"source":"dbSNP","strand":1,"feature_type":"variation","end":140436326,"alleles":["A","T"]},{"start":140436329,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","A","T"],"end":140436329,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs919889618","clinical_significance":[]},{"id":"rs1799777668","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140436331,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436331,"source":"dbSNP"},{"start":140436333,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140436333,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799777690","clinical_significance":[]},{"clinical_significance":[],"id":"rs761790411","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436335,"feature_type":"variation","strand":1,"end":140436335,"alleles":["C","A"]},{"strand":1,"feature_type":"variation","end":140436336,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436336,"source":"dbSNP","seq_region_name":"7","id":"rs889976065","clinical_significance":[]},{"clinical_significance":[],"id":"rs550286679","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436336,"feature_type":"variation","strand":1,"alleles":["TCAATCAATC","TCAATC"],"end":140436345},{"clinical_significance":[],"id":"rs186319393","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140436337,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436337},{"alleles":["A","G"],"end":140436339,"feature_type":"variation","strand":1,"source":"dbSNP","start":140436339,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs148659373"},{"id":"rs1022983399","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140436341,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436341,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140436343,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436343,"clinical_significance":[],"seq_region_name":"7","id":"rs35747234"},{"seq_region_name":"7","id":"rs944234860","clinical_significance":[],"start":140436346,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140436346,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1799777973","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436349,"source":"dbSNP","strand":1,"feature_type":"variation","end":140436349,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs137862227","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436349,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CAGCCTCAGCCTCA","CAGCCTCAGCCTCAGCCTCA"],"end":140436362},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799778032","feature_type":"variation","strand":1,"alleles":["T","A"],"end":140436354,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436354},{"source":"dbSNP","start":140436359,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140436359,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585445119"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799778064","feature_type":"variation","strand":1,"end":140436361,"alleles":["C","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436361},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436363,"source":"dbSNP","strand":1,"feature_type":"variation","end":140436363,"alleles":["C","G","T"],"seq_region_name":"7","id":"rs1345389600","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799778121","clinical_significance":[],"start":140436364,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140436364,"alleles":["G","A","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799778139","feature_type":"variation","strand":1,"alleles":["A","T"],"end":140436371,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436371},{"clinical_significance":[],"seq_region_name":"7","id":"rs192325436","alleles":["G","A"],"end":140436372,"feature_type":"variation","strand":1,"source":"dbSNP","start":140436372,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"id":"rs2130196170","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140436373,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436373,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799778184","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436374,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140436374},{"alleles":["G","A"],"end":140436378,"strand":1,"feature_type":"variation","start":140436378,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799778211","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1404087276","source":"dbSNP","start":140436379,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140436379,"alleles":["G","A"],"feature_type":"variation","strand":1},{"end":140436380,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140436380,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799778256","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436383,"feature_type":"variation","strand":1,"end":140436383,"alleles":["C","T"],"clinical_significance":[],"id":"rs978163890","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs28573207","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436384,"feature_type":"variation","strand":1,"end":140436384,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1799778329","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436385,"source":"dbSNP","strand":1,"feature_type":"variation","end":140436385,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799778346","end":140436386,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140436386,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1162347223","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140436387,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436387,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1585445140","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140436389,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436389,"source":"dbSNP"},{"end":140436396,"alleles":["A","G","T"],"strand":1,"feature_type":"variation","start":140436396,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs960351711","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799778419","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436397,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140436397},{"strand":1,"feature_type":"variation","end":140436402,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436402,"source":"dbSNP","id":"rs539263271","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs991946928","feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140436404,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436404},{"strand":1,"feature_type":"variation","end":140436405,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436405,"source":"dbSNP","id":"rs1799778492","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1480153241","clinical_significance":[],"end":140436411,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140436411,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140436412,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436412,"source":"dbSNP","id":"rs1585445152","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1247052854","clinical_significance":[],"start":140436413,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140436413,"strand":1,"feature_type":"variation"},{"end":140436417,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140436417,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1223578312"},{"strand":1,"feature_type":"variation","end":140436420,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436420,"source":"dbSNP","seq_region_name":"7","id":"rs900097783","clinical_significance":[]},{"seq_region_name":"7","id":"rs1011809441","clinical_significance":[],"end":140436421,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140436421,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799778652","feature_type":"variation","strand":1,"end":140436424,"alleles":["A","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436424},{"seq_region_name":"7","id":"rs1259722325","clinical_significance":[],"start":140436425,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140436425,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1240906633","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436426,"feature_type":"variation","strand":1,"end":140436426,"alleles":["T","TT"]},{"seq_region_name":"7","id":"rs1799778721","clinical_significance":[],"strand":1,"feature_type":"variation","end":140436427,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436427,"source":"dbSNP"},{"id":"rs1585445168","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140436430,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436430,"source":"dbSNP"},{"seq_region_name":"7","id":"rs765957039","clinical_significance":[],"end":140436433,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140436433,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"start":140436443,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140436443,"alleles":["T","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1307271546","clinical_significance":[]},{"id":"rs1043791335","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140436444,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436444,"source":"dbSNP"},{"start":140436445,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140436445,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1368649839","clinical_significance":[]},{"clinical_significance":[],"id":"rs1174774674","seq_region_name":"7","source":"dbSNP","start":140436448,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140436448,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1397274681","clinical_significance":[],"start":140436452,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A","T"],"end":140436452,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799778926","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436454,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140436454},{"clinical_significance":[],"seq_region_name":"7","id":"rs1349757739","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436457,"feature_type":"variation","strand":1,"end":140436457,"alleles":["G","A"]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436458,"source":"dbSNP","strand":1,"feature_type":"variation","end":140436458,"alleles":["G","A"],"seq_region_name":"7","id":"rs1799778973","clinical_significance":[]},{"seq_region_name":"7","id":"rs1299372638","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436463,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140436463},{"alleles":["G","A"],"end":140436464,"feature_type":"variation","strand":1,"source":"dbSNP","start":140436464,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs903554363","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs556794664","source":"dbSNP","start":140436466,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140436466,"feature_type":"variation","strand":1},{"alleles":["G","A","C"],"end":140436467,"strand":1,"feature_type":"variation","start":140436467,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs182564934","clinical_significance":[]},{"id":"rs1418143781","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140436469,"strand":1,"feature_type":"variation","start":140436469,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"end":140436479,"alleles":["TTCTTCTTC","TTCTTC"],"strand":1,"feature_type":"variation","start":140436471,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799779122","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1425480951","source":"dbSNP","start":140436472,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140436472,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs536014695","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140436482,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436482},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140436488,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436488,"clinical_significance":[],"id":"rs2130196318","seq_region_name":"7"},{"end":140436490,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140436490,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs960429068","clinical_significance":[]},{"source":"dbSNP","start":140436491,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140436491,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs909138057","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1268048087","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436492,"source":"dbSNP","strand":1,"feature_type":"variation","end":140436497,"alleles":["TTCTTT","TT"]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436499,"feature_type":"variation","strand":1,"end":140436499,"alleles":["T","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799779217"},{"feature_type":"variation","strand":1,"end":140436500,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436500,"clinical_significance":[],"seq_region_name":"7","id":"rs186250682"},{"strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140436501,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436501,"source":"dbSNP","id":"rs767174113","seq_region_name":"7","clinical_significance":[]},{"end":140436502,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140436502,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1283960560","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1286659264","clinical_significance":[],"alleles":["T","C","G"],"end":140436504,"strand":1,"feature_type":"variation","start":140436504,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436504,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TC","TCTC"],"end":140436505,"seq_region_name":"7","id":"rs1799779347","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1360601441","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436509,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140436509},{"start":140436514,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140436514,"strand":1,"feature_type":"variation","id":"rs1799779390","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs969711289","seq_region_name":"7","end":140436515,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140436515,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1367349234","clinical_significance":[],"end":140436516,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140436516,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"id":"rs973984867","seq_region_name":"7","source":"dbSNP","start":140436518,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140436518,"alleles":["T","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1799779444","clinical_significance":[],"alleles":["T","C"],"end":140436523,"strand":1,"feature_type":"variation","start":140436523,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"strand":1,"feature_type":"variation","end":140436528,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436528,"source":"dbSNP","seq_region_name":"7","id":"rs897194502","clinical_significance":[]},{"source":"dbSNP","start":140436530,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140436530,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs753232810"},{"clinical_significance":[],"id":"rs1799779503","seq_region_name":"7","end":140436535,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140436535,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs951424574","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436537,"source":"dbSNP","strand":1,"feature_type":"variation","end":140436537,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs1799779547","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436538,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140436538},{"seq_region_name":"7","id":"rs1799779574","clinical_significance":[],"strand":1,"feature_type":"variation","end":140436540,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436540,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1295777894","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436543,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140436543},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436547,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140436547,"seq_region_name":"7","id":"rs1051153672","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436550,"feature_type":"variation","strand":1,"end":140436550,"alleles":["T","C"],"clinical_significance":[],"id":"rs1359329379","seq_region_name":"7"},{"start":140436551,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","G","T"],"end":140436551,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs767244778","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1368681166","source":"dbSNP","start":140436556,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140436556,"alleles":["A","G"],"feature_type":"variation","strand":1},{"alleles":["C","T"],"end":140436570,"strand":1,"feature_type":"variation","start":140436570,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1007031609","clinical_significance":[]},{"seq_region_name":"7","id":"rs1040296027","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["TATTTAT","TAT"],"end":140436577,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436571,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799780135","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140436572,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436572},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436574,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140436574,"clinical_significance":[],"seq_region_name":"7","id":"rs142186115"},{"source":"dbSNP","start":140436576,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140436576,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs372249418","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1483636270","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436577,"source":"dbSNP","strand":1,"feature_type":"variation","end":140436577,"alleles":["T","C"]},{"clinical_significance":[],"id":"rs1257909491","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436579,"feature_type":"variation","strand":1,"end":140436579,"alleles":["A","T"]},{"seq_region_name":"7","id":"rs1799780366","clinical_significance":[],"start":140436580,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140436580,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1799780386","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140436581,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436581,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140436582,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436582,"clinical_significance":[],"seq_region_name":"7","id":"rs2130196467"},{"strand":1,"feature_type":"variation","end":140436587,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436587,"source":"dbSNP","id":"rs1799780413","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1208297225","source":"dbSNP","start":140436589,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140436589,"alleles":["A","G","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799780459","alleles":["A","T"],"end":140436590,"feature_type":"variation","strand":1,"source":"dbSNP","start":140436590,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"id":"rs540749536","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140436591,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436591,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799780494","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140436595,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436595,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436596,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140436596,"seq_region_name":"7","id":"rs1799780518","clinical_significance":[]},{"alleles":["A","G"],"end":140436599,"strand":1,"feature_type":"variation","start":140436599,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1259103680","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436600,"source":"dbSNP","strand":1,"feature_type":"variation","end":140436600,"alleles":["T","C"],"seq_region_name":"7","id":"rs1220891287","clinical_significance":[]},{"source":"dbSNP","start":140436606,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140436606,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799780582"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1339060762","source":"dbSNP","start":140436610,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140436610,"feature_type":"variation","strand":1},{"start":140436611,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","C"],"end":140436611,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs999814382","clinical_significance":[]},{"alleles":["C","CC"],"end":140436615,"strand":1,"feature_type":"variation","start":140436615,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799780648","clinical_significance":[]},{"alleles":["T","A"],"end":140436626,"feature_type":"variation","strand":1,"source":"dbSNP","start":140436626,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1218158190"},{"seq_region_name":"7","id":"rs1381124976","clinical_significance":[],"strand":1,"feature_type":"variation","end":140436632,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436632,"source":"dbSNP"},{"seq_region_name":"7","id":"rs778134587","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436633,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140436633},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140436641,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436641,"clinical_significance":[],"seq_region_name":"7","id":"rs1799780729"},{"end":140436646,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140436646,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799780746"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436648,"feature_type":"variation","strand":1,"end":140436648,"alleles":["T","A","C"],"clinical_significance":[],"id":"rs903417286","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1464222243","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436655,"feature_type":"variation","strand":1,"end":140436655,"alleles":["A","G"]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436657,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140436657,"clinical_significance":[],"seq_region_name":"7","id":"rs999218381"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130196541","source":"dbSNP","start":140436660,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140436660,"alleles":["C","A"],"feature_type":"variation","strand":1},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436661,"feature_type":"variation","strand":1,"end":140436661,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs750177007"},{"alleles":["G","A"],"end":140436662,"strand":1,"feature_type":"variation","start":140436662,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1467008981","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799780863","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140436664,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436664},{"seq_region_name":"7","id":"rs896253318","clinical_significance":[],"strand":1,"feature_type":"variation","end":140436668,"alleles":["CCCCC","CCCC"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436664,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799780912","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436668,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140436668},{"end":140436670,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140436670,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs551523724","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140436672,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436672,"source":"dbSNP","id":"rs1013243799","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140436675,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140436675,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1023899507"},{"source":"dbSNP","start":140436678,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140436678,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs558678572"},{"clinical_significance":[],"id":"rs10250996","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436679,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140436679},{"seq_region_name":"7","id":"rs1239068628","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436680,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140436680},{"id":"rs985039781","seq_region_name":"7","clinical_significance":[],"start":140436682,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140436682,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1799781158","clinical_significance":[],"alleles":["T","C","G"],"end":140436689,"strand":1,"feature_type":"variation","start":140436689,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1316480826","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436689,"source":"dbSNP","strand":1,"feature_type":"variation","end":140436690,"alleles":["TT","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799781201","end":140436692,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140436692,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140436696,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140436696,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585445347"},{"clinical_significance":[],"id":"rs909083038","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436698,"feature_type":"variation","strand":1,"end":140436698,"alleles":["C","G","T"]},{"clinical_significance":[],"id":"rs1799781249","seq_region_name":"7","source":"dbSNP","start":140436699,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140436699,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1453109823","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436703,"feature_type":"variation","strand":1,"end":140436706,"alleles":["CCCC","CCCCC"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs962184189","alleles":["C","A"],"end":140436706,"feature_type":"variation","strand":1,"source":"dbSNP","start":140436706,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1246185506","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140436709,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436709},{"id":"rs972031803","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140436710,"strand":1,"feature_type":"variation","start":140436710,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799781345","source":"dbSNP","start":140436713,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140436713,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1193444808","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436723,"feature_type":"variation","strand":1,"end":140436723,"alleles":["C","T"]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436726,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140436726,"seq_region_name":"7","id":"rs1409144448","clinical_significance":[]},{"clinical_significance":[],"id":"rs544620190","seq_region_name":"7","feature_type":"variation","strand":1,"end":140436727,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436727},{"id":"rs923178964","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140436728,"strand":1,"feature_type":"variation","start":140436728,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs563148288","clinical_significance":[],"strand":1,"feature_type":"variation","end":140436730,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436730,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140436731,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436731,"source":"dbSNP","id":"rs934007338","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["AGAG","AG"],"end":140436737,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436734,"clinical_significance":[],"seq_region_name":"7","id":"rs1449888175"},{"alleles":["G","A"],"end":140436735,"feature_type":"variation","strand":1,"source":"dbSNP","start":140436735,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799781502"},{"alleles":["G","A"],"end":140436737,"feature_type":"variation","strand":1,"source":"dbSNP","start":140436737,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799781525"},{"seq_region_name":"7","id":"rs1381562384","clinical_significance":[],"start":140436745,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140436745,"strand":1,"feature_type":"variation"},{"start":140436746,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140436746,"alleles":["C","G"],"strand":1,"feature_type":"variation","id":"rs1420526222","seq_region_name":"7","clinical_significance":[]},{"id":"rs1167168787","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140436747,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436747,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1331648687","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436747,"source":"dbSNP","strand":1,"feature_type":"variation","end":140436751,"alleles":["TTTTT","TTT","TTTTTT"]},{"alleles":["T","G"],"end":140436750,"strand":1,"feature_type":"variation","start":140436750,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1799781617","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs62490415","source":"dbSNP","start":140436764,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140436764,"alleles":["G","A","C"],"feature_type":"variation","strand":1},{"alleles":["T","C"],"end":140436768,"feature_type":"variation","strand":1,"source":"dbSNP","start":140436768,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs527800344"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799781709","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436770,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140436770},{"seq_region_name":"7","id":"rs2130196685","clinical_significance":[],"alleles":["C","G"],"end":140436776,"strand":1,"feature_type":"variation","start":140436776,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436777,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140436777,"clinical_significance":[],"seq_region_name":"7","id":"rs942765855"},{"end":140436778,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140436778,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs2130196692","seq_region_name":"7"},{"source":"dbSNP","start":140436781,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140436781,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1444108816","seq_region_name":"7"},{"seq_region_name":"7","id":"rs912540038","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140436782,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436782,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140436785,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436785,"source":"dbSNP","seq_region_name":"7","id":"rs1180750846","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1456677883","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436788,"feature_type":"variation","strand":1,"end":140436788,"alleles":["T","A"]},{"start":140436789,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140436789,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799781829","clinical_significance":[]},{"id":"rs1250246128","seq_region_name":"7","clinical_significance":[],"end":140436795,"alleles":["AAAAAA","AAAAAAA"],"strand":1,"feature_type":"variation","start":140436790,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"id":"rs1461562049","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140436796,"alleles":["T","C","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436796,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1489738359","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436801,"source":"dbSNP","strand":1,"feature_type":"variation","end":140436801,"alleles":["T","C"]},{"start":140436802,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140436802,"alleles":["T","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799781899","clinical_significance":[]},{"clinical_significance":[],"id":"rs1327328571","seq_region_name":"7","alleles":["TCTTCTT","TCTT"],"end":140436811,"feature_type":"variation","strand":1,"source":"dbSNP","start":140436805,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799781929","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140436806,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436806},{"source":"dbSNP","start":140436807,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140436807,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1243079962"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1264256081","end":140436812,"alleles":["TTCTTT","TT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140436807,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1799781993","clinical_significance":[],"strand":1,"feature_type":"variation","end":140436809,"alleles":["C","-"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436809,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799782011","end":140436809,"alleles":["-","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140436810,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436810,"source":"dbSNP","strand":1,"feature_type":"variation","end":140436810,"alleles":["T","C"],"seq_region_name":"7","id":"rs1585445418","clinical_significance":[]},{"id":"rs33999792","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["TTTTTTTTTTTTT","TTTTTTTTTTT","TTTTTTTTTTTT","TTTTTTTTTTTTTT","TTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTT"],"end":140436822,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436810,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799782541","clinical_significance":[],"start":140436812,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140436812,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs74361451","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436822,"source":"dbSNP","strand":1,"feature_type":"variation","end":140436822,"alleles":["T","A"]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436823,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140436823,"seq_region_name":"7","id":"rs1392252827","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799782620","end":140436824,"alleles":["AA","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140436823,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"start":140436824,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140436824,"alleles":["A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs200008313","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1440056301","source":"dbSNP","start":140436830,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140436830,"feature_type":"variation","strand":1},{"id":"rs1799782699","seq_region_name":"7","clinical_significance":[],"start":140436831,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140436831,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799782716","feature_type":"variation","strand":1,"end":140436835,"alleles":["A","AA"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436835},{"seq_region_name":"7","id":"rs1301250166","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["AGAG","AG"],"end":140436838,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436835,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799782766","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140436841,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436841,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1424023546","clinical_significance":[],"alleles":["C","T"],"end":140436844,"strand":1,"feature_type":"variation","start":140436844,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1279948694","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436847,"feature_type":"variation","strand":1,"end":140436847,"alleles":["T","C"]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436848,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140436848,"seq_region_name":"7","id":"rs965849021","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130196817","clinical_significance":[],"strand":1,"feature_type":"variation","end":140436858,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436858,"source":"dbSNP"},{"source":"dbSNP","start":140436860,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140436860,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799782856","seq_region_name":"7"},{"alleles":["G","A"],"end":140436861,"strand":1,"feature_type":"variation","start":140436861,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1585445441","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436863,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140436863,"clinical_significance":[],"seq_region_name":"7","id":"rs1799782907"},{"end":140436866,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140436866,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1225692252"},{"id":"rs1305060611","seq_region_name":"7","clinical_significance":[],"start":140436870,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140436870,"strand":1,"feature_type":"variation"},{"start":140436874,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140436874,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs866295641","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1328731350","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436875,"feature_type":"variation","strand":1,"end":140436875,"alleles":["G","A"]},{"end":140436877,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140436877,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799782970","clinical_significance":[]},{"alleles":["G","A","C"],"end":140436882,"feature_type":"variation","strand":1,"source":"dbSNP","start":140436882,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799782984"},{"id":"rs1200003162","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140436885,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436885,"source":"dbSNP"},{"clinical_significance":[],"id":"rs904059042","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140436886,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436886},{"seq_region_name":"7","id":"rs1435304553","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436888,"source":"dbSNP","strand":1,"feature_type":"variation","end":140436888,"alleles":["T","C"]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436893,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140436893,"id":"rs1000083170","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs191118549","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140436897,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436897},{"clinical_significance":[],"seq_region_name":"7","id":"rs1222413686","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436898,"feature_type":"variation","strand":1,"end":140436898,"alleles":["G","A","T"]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436899,"source":"dbSNP","strand":1,"feature_type":"variation","end":140436899,"alleles":["C","T"],"seq_region_name":"7","id":"rs1799783165","clinical_significance":[]},{"alleles":["C","T"],"end":140436900,"feature_type":"variation","strand":1,"source":"dbSNP","start":140436900,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1467562402"},{"end":140436904,"alleles":["T","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140436904,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs528168729"},{"feature_type":"variation","strand":1,"end":140436907,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436907,"clinical_significance":[],"seq_region_name":"7","id":"rs1286101219"},{"seq_region_name":"7","id":"rs1585445476","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140436908,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436908,"source":"dbSNP"},{"alleles":["G","A"],"end":140436913,"feature_type":"variation","strand":1,"source":"dbSNP","start":140436913,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799783275"},{"seq_region_name":"7","id":"rs1213562136","clinical_significance":[],"start":140436915,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140436916,"alleles":["AA","A"],"strand":1,"feature_type":"variation"},{"id":"rs1799783314","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140436918,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436918,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799783359","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436919,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140436919},{"id":"rs1799783379","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","-"],"end":140436919,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436919,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs896709379","end":140436920,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140436920,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130196903","feature_type":"variation","strand":1,"end":140436930,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436930},{"end":140436931,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140436931,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1799783416","seq_region_name":"7","clinical_significance":[]},{"end":140436934,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140436934,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs546712769"},{"seq_region_name":"7","id":"rs1799783458","clinical_significance":[],"start":140436940,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140436940,"strand":1,"feature_type":"variation"},{"end":140436944,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140436944,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799783469"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140436945,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140436945,"clinical_significance":[],"seq_region_name":"7","id":"rs1799783488"},{"start":140436946,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140436946,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs182634960","clinical_significance":[]},{"seq_region_name":"7","id":"rs531936846","clinical_significance":[],"start":140436947,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140436947,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"start":140436955,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A","T"],"end":140436955,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs969037829","clinical_significance":[]},{"source":"dbSNP","start":140436956,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140436956,"alleles":["T","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs10272520","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436957,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140436957,"seq_region_name":"7","id":"rs1404245552","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs758533792","end":140436962,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140436962,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"alleles":["G","A"],"end":140436973,"strand":1,"feature_type":"variation","start":140436973,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1361165941","clinical_significance":[]},{"start":140436979,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["TTTTT","TTTT"],"end":140436983,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799783697","clinical_significance":[]},{"source":"dbSNP","start":140436984,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140436984,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs12216619"},{"strand":1,"feature_type":"variation","end":140436985,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436985,"source":"dbSNP","seq_region_name":"7","id":"rs34693155","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140436987,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140436987,"seq_region_name":"7","id":"rs1799783822","clinical_significance":[]},{"source":"dbSNP","start":140436993,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140436993,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs2130196982","seq_region_name":"7"},{"clinical_significance":[],"id":"rs538221846","seq_region_name":"7","end":140437000,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140437000,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"start":140437001,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140437001,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799783859","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799783878","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140437002,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437002},{"feature_type":"variation","strand":1,"alleles":["G","C","T"],"end":140437003,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437003,"clinical_significance":[],"seq_region_name":"7","id":"rs1799783901"},{"seq_region_name":"7","id":"rs556730121","clinical_significance":[],"start":140437006,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140437006,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140437007,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437007,"clinical_significance":[],"seq_region_name":"7","id":"rs1799783949"},{"feature_type":"variation","strand":1,"end":140437011,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437011,"clinical_significance":[],"seq_region_name":"7","id":"rs1799783969"},{"seq_region_name":"7","id":"rs1799783989","clinical_significance":[],"alleles":["G","A"],"end":140437015,"strand":1,"feature_type":"variation","start":140437015,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799784007","source":"dbSNP","start":140437018,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140437018,"alleles":["C","T"],"feature_type":"variation","strand":1},{"end":140437022,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140437022,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs145299137","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1427618960","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437023,"feature_type":"variation","strand":1,"alleles":["G","A","C","T"],"end":140437023},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140437025,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437025,"source":"dbSNP","seq_region_name":"7","id":"rs757454378","clinical_significance":[]},{"start":140437035,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","C"],"end":140437035,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1478416119","clinical_significance":[]},{"seq_region_name":"7","id":"rs80148145","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437037,"source":"dbSNP","strand":1,"feature_type":"variation","end":140437037,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1799784261","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140437038,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437038,"source":"dbSNP"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437041,"feature_type":"variation","strand":1,"end":140437041,"alleles":["G","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs75278764"},{"clinical_significance":[],"id":"rs1799784349","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437050,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140437050},{"source":"dbSNP","start":140437057,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140437057,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585445553"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1283037786","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437062,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140437062},{"id":"rs1200691036","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["-","TGAGGATC"],"end":140437071,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437072,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1297387627","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437072,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140437072},{"start":140437075,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140437075,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130197062","clinical_significance":[]},{"clinical_significance":[],"id":"rs904924104","seq_region_name":"7","end":140437080,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140437080,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1234105122","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140437086,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437086},{"seq_region_name":"7","id":"rs1043840246","clinical_significance":[],"start":140437089,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140437089,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140437098,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437098,"clinical_significance":[],"seq_region_name":"7","id":"rs1799784536"},{"id":"rs1341031285","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437105,"source":"dbSNP","strand":1,"feature_type":"variation","end":140437105,"alleles":["C","A"]},{"alleles":["G","A"],"end":140437110,"feature_type":"variation","strand":1,"source":"dbSNP","start":140437110,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs995383966"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437112,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140437112,"seq_region_name":"7","id":"rs187099108","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140437114,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437114,"clinical_significance":[],"seq_region_name":"7","id":"rs935525322"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130197097","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437116,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140437116},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799785592","source":"dbSNP","start":140437118,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140437118,"alleles":["A","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1325941480","seq_region_name":"7","end":140437121,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140437121,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437122,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140437122,"seq_region_name":"7","id":"rs577436403","clinical_significance":[]},{"clinical_significance":[],"id":"rs774115096","seq_region_name":"7","alleles":["C","A","T"],"end":140437124,"feature_type":"variation","strand":1,"source":"dbSNP","start":140437124,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs896740487","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437125,"source":"dbSNP","strand":1,"feature_type":"variation","end":140437125,"alleles":["G","A"]},{"end":140437126,"alleles":["T","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140437126,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1404272907","seq_region_name":"7"},{"clinical_significance":[],"id":"rs949653023","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437127,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140437127},{"start":140437130,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140437130,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1045341344","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1004048234","source":"dbSNP","start":140437133,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140437133,"alleles":["A","C"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437136,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140437136,"seq_region_name":"7","id":"rs1585445589","clinical_significance":[]},{"clinical_significance":[],"id":"rs78736050","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","A","C","G"],"end":140437137,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437137},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437140,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140437140,"clinical_significance":[],"id":"rs556628123","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799785955","clinical_significance":[],"start":140437140,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140437149,"alleles":["ATTATGAAAA","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs2130197161","clinical_significance":[],"end":140437141,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140437141,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140437143,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437143,"clinical_significance":[],"seq_region_name":"7","id":"rs2130197165"},{"seq_region_name":"7","id":"rs1251519752","clinical_significance":[],"start":140437144,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140437144,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs2130197171","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437145,"source":"dbSNP","strand":1,"feature_type":"variation","end":140437145,"alleles":["G","A"]},{"feature_type":"variation","strand":1,"end":140437147,"alleles":["A","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437147,"clinical_significance":[],"seq_region_name":"7","id":"rs575164035"},{"source":"dbSNP","start":140437148,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140437148,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130197182"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437156,"feature_type":"variation","strand":1,"end":140437156,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1485809034"},{"alleles":["C","A"],"end":140437160,"strand":1,"feature_type":"variation","start":140437160,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1187686481","clinical_significance":[]},{"clinical_significance":[],"id":"rs1189579360","seq_region_name":"7","alleles":["AGAAAGAA","AGAA"],"end":140437168,"feature_type":"variation","strand":1,"source":"dbSNP","start":140437161,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437166,"source":"dbSNP","strand":1,"feature_type":"variation","end":140437166,"alleles":["G","-"],"seq_region_name":"7","id":"rs1254787046","clinical_significance":[]},{"start":140437169,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140437169,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1016029180","clinical_significance":[]},{"source":"dbSNP","start":140437179,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140437179,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1318336161"},{"alleles":["G","C"],"end":140437181,"strand":1,"feature_type":"variation","start":140437181,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799786163","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799786184","clinical_significance":[],"strand":1,"feature_type":"variation","end":140437184,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437184,"source":"dbSNP"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437187,"feature_type":"variation","strand":1,"end":140437187,"alleles":["T","C"],"clinical_significance":[],"id":"rs1799786203","seq_region_name":"7"},{"source":"dbSNP","start":140437189,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140437189,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799786218"},{"seq_region_name":"7","id":"rs975801126","clinical_significance":[],"strand":1,"feature_type":"variation","end":140437193,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437193,"source":"dbSNP"},{"clinical_significance":[],"id":"rs10272791","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437195,"feature_type":"variation","strand":1,"end":140437195,"alleles":["T","A","C"]},{"feature_type":"variation","strand":1,"end":140437203,"alleles":["CATCA","CATCATCA"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437199,"clinical_significance":[],"seq_region_name":"7","id":"rs1799786352"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1212718190","alleles":["CATCACCCACAT","CAT"],"end":140437210,"feature_type":"variation","strand":1,"source":"dbSNP","start":140437199,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"id":"rs1799786400","seq_region_name":"7","clinical_significance":[],"end":140437206,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140437206,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"feature_type":"variation","strand":1,"end":140437208,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437208,"clinical_significance":[],"seq_region_name":"7","id":"rs1338715858"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437208,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","-"],"end":140437208,"seq_region_name":"7","id":"rs1799786430","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs543348909","source":"dbSNP","start":140437210,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140437210,"feature_type":"variation","strand":1},{"end":140437214,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140437214,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799786463","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs560508906","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437220,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140437220},{"seq_region_name":"7","id":"rs1799786507","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437224,"source":"dbSNP","strand":1,"feature_type":"variation","end":140437227,"alleles":["TTTT","TT"]},{"source":"dbSNP","start":140437230,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140437230,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs572557475"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140437232,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437232,"clinical_significance":[],"seq_region_name":"7","id":"rs1284852910"},{"seq_region_name":"7","id":"rs183099268","clinical_significance":[],"end":140437234,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140437234,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"start":140437235,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C","G"],"end":140437235,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs878935428","clinical_significance":[]},{"seq_region_name":"7","id":"rs1421642073","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140437240,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437240,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1336329068","feature_type":"variation","strand":1,"end":140437241,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437241},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437242,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140437242,"clinical_significance":[],"id":"rs1585445663","seq_region_name":"7"},{"alleles":["T","C"],"end":140437243,"strand":1,"feature_type":"variation","start":140437243,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs530169287","seq_region_name":"7","clinical_significance":[]},{"end":140437245,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140437245,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799786933","clinical_significance":[]},{"alleles":["T","A"],"end":140437252,"strand":1,"feature_type":"variation","start":140437252,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799786956","clinical_significance":[]},{"id":"rs954535862","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140437254,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437254,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437256,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140437256,"seq_region_name":"7","id":"rs978941836","clinical_significance":[]},{"seq_region_name":"7","id":"rs1409863672","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437260,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140437260},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799787057","source":"dbSNP","start":140437262,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140437262,"alleles":["A","AA"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1169539965","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140437263,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437263},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437266,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140437266,"clinical_significance":[],"seq_region_name":"7","id":"rs1445937818"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799787137","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140437268,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437268},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585445687","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437269,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140437269},{"alleles":["T","G"],"end":140437270,"feature_type":"variation","strand":1,"source":"dbSNP","start":140437270,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs761187508"},{"feature_type":"variation","strand":1,"end":140437271,"alleles":["C","A","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437271,"clinical_significance":[],"id":"rs1799787212","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799787242","clinical_significance":[],"alleles":["CAGCCCCCCA","CA"],"end":140437280,"strand":1,"feature_type":"variation","start":140437271,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"id":"rs1799787268","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140437272,"alleles":["-","ATTTTTAACAT"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437273,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799787292","clinical_significance":[],"start":140437274,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140437274,"strand":1,"feature_type":"variation"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437275,"feature_type":"variation","strand":1,"alleles":["-","ATTT"],"end":140437274,"clinical_significance":[],"seq_region_name":"7","id":"rs1799787308"},{"clinical_significance":[],"id":"rs1799787331","seq_region_name":"7","feature_type":"variation","strand":1,"end":140437277,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437277},{"clinical_significance":[],"seq_region_name":"7","id":"rs1415659191","feature_type":"variation","strand":1,"end":140437278,"alleles":["C","A","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437278},{"id":"rs1182626362","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140437279,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437279,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1017456634","clinical_significance":[],"start":140437280,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140437280,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1457977073","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["AAA","AA","AAAA"],"end":140437282,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437280},{"seq_region_name":"7","id":"rs1799787458","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437282,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140437282},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437286,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140437286,"seq_region_name":"7","id":"rs1585445697","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1202268605","source":"dbSNP","start":140437287,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140437287,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799787524","alleles":["C","T"],"end":140437289,"feature_type":"variation","strand":1,"source":"dbSNP","start":140437289,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs924732024","clinical_significance":[],"start":140437291,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","G"],"end":140437291,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1353784545","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437292,"source":"dbSNP","strand":1,"feature_type":"variation","end":140437292,"alleles":["G","T"]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140437299,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437299,"source":"dbSNP","id":"rs964105693","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs979810055","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437308,"source":"dbSNP","strand":1,"feature_type":"variation","end":140437308,"alleles":["A","C"]},{"alleles":["T","C"],"end":140437315,"feature_type":"variation","strand":1,"source":"dbSNP","start":140437315,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1357411864"},{"seq_region_name":"7","id":"rs1799787669","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437316,"source":"dbSNP","strand":1,"feature_type":"variation","end":140437316,"alleles":["C","T"]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437316,"feature_type":"variation","strand":1,"end":140437320,"alleles":["CTCCT","CT"],"clinical_significance":[],"id":"rs1799787691","seq_region_name":"7"},{"end":140437319,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140437319,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799787714","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799787737","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437321,"feature_type":"variation","strand":1,"end":140437321,"alleles":["A","G"]},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140437322,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437322,"clinical_significance":[],"seq_region_name":"7","id":"rs925406985"},{"seq_region_name":"7","id":"rs1241118888","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437323,"source":"dbSNP","strand":1,"feature_type":"variation","end":140437323,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1379444922","end":140437326,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140437326,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437331,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140437331,"clinical_significance":[],"id":"rs1296803509","seq_region_name":"7"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437333,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140437333,"clinical_significance":[],"seq_region_name":"7","id":"rs1442005593"},{"source":"dbSNP","start":140437334,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140437334,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1342147765"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437335,"feature_type":"variation","strand":1,"end":140437335,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1213277227"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140437337,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437337,"clinical_significance":[],"seq_region_name":"7","id":"rs935372569"},{"start":140437341,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140437341,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs117717507","clinical_significance":[]},{"end":140437342,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140437342,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799788002","clinical_significance":[]},{"alleles":["C","G","T"],"end":140437343,"strand":1,"feature_type":"variation","start":140437343,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs147656574","clinical_significance":[]},{"source":"dbSNP","start":140437344,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140437344,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs754194677"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437346,"source":"dbSNP","strand":1,"feature_type":"variation","end":140437346,"alleles":["T","C"],"id":"rs1348971814","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","C"],"end":140437347,"feature_type":"variation","strand":1,"source":"dbSNP","start":140437347,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1162424125"},{"seq_region_name":"7","id":"rs1439919849","clinical_significance":[],"start":140437351,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140437351,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140437357,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437357,"source":"dbSNP","seq_region_name":"7","id":"rs1212600562","clinical_significance":[]},{"alleles":["C","-"],"end":140437358,"feature_type":"variation","strand":1,"source":"dbSNP","start":140437358,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799788179"},{"clinical_significance":[],"id":"rs1799788205","seq_region_name":"7","feature_type":"variation","strand":1,"end":140437366,"alleles":["G","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437366},{"clinical_significance":[],"seq_region_name":"7","id":"rs757535886","alleles":["C","A","T"],"end":140437370,"feature_type":"variation","strand":1,"source":"dbSNP","start":140437370,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1799788256","clinical_significance":[],"start":140437371,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","T"],"end":140437371,"strand":1,"feature_type":"variation"},{"id":"rs1799788270","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437376,"source":"dbSNP","strand":1,"feature_type":"variation","end":140437376,"alleles":["C","T"]},{"id":"rs1469443412","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140437378,"strand":1,"feature_type":"variation","start":140437378,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1799788318","clinical_significance":[],"start":140437379,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140437379,"strand":1,"feature_type":"variation"},{"end":140437383,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140437383,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1247174765"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130197481","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437385,"feature_type":"variation","strand":1,"end":140437385,"alleles":["C","T"]},{"strand":1,"feature_type":"variation","alleles":["G","A","C","T"],"end":140437386,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437386,"source":"dbSNP","seq_region_name":"7","id":"rs905416188","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140437393,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437393,"clinical_significance":[],"seq_region_name":"7","id":"rs1799788399"},{"end":140437394,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140437394,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799788424"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799788442","end":140437397,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140437397,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"end":140437401,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140437401,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799788465"},{"source":"dbSNP","start":140437403,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140437403,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs140957971"},{"end":140437404,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140437404,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1243320367","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437411,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140437411,"seq_region_name":"7","id":"rs549321200","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140437412,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437412,"source":"dbSNP","seq_region_name":"7","id":"rs897582709","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140437413,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437413,"source":"dbSNP","seq_region_name":"7","id":"rs1799788605","clinical_significance":[]},{"start":140437414,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["TGAGCCAAGATGGTGCCACTGCACT","T"],"end":140437438,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799788628","clinical_significance":[]},{"clinical_significance":[],"id":"rs1585445767","seq_region_name":"7","source":"dbSNP","start":140437419,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140437419,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1799788672","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140437425,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437425,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437426,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140437426,"seq_region_name":"7","id":"rs993241290","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs562174692","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437429,"feature_type":"variation","strand":1,"end":140437429,"alleles":["C","G","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799788743","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437432,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140437432},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437433,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140437433,"clinical_significance":[],"id":"rs1799788777","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1368783858","clinical_significance":[],"start":140437437,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140437437,"strand":1,"feature_type":"variation"},{"start":140437439,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","A","T"],"end":140437439,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1030034504","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140437440,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437440,"source":"dbSNP","seq_region_name":"7","id":"rs529943394","clinical_significance":[]},{"id":"rs1301977923","seq_region_name":"7","clinical_significance":[],"end":140437442,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140437442,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"strand":1,"feature_type":"variation","alleles":["GCCTGGGCAAC","GCCTGGGCAACGCCTGGGCAAC"],"end":140437452,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437442,"source":"dbSNP","seq_region_name":"7","id":"rs1799788912","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563079610","alleles":["C","T"],"end":140437444,"feature_type":"variation","strand":1,"source":"dbSNP","start":140437444,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1007334301","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140437449,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437449},{"end":140437452,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140437452,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799788982","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1414102551","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140437454,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437454},{"source":"dbSNP","start":140437455,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140437455,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1563079620"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140437457,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437457,"clinical_significance":[],"seq_region_name":"7","id":"rs548505537"},{"source":"dbSNP","start":140437458,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140437461,"alleles":["GAGA","GAGAGA"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799789067"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437462,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140437462,"clinical_significance":[],"id":"rs1319092588","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1419795213","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437463,"source":"dbSNP","strand":1,"feature_type":"variation","end":140437463,"alleles":["C","G","T"]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437471,"feature_type":"variation","strand":1,"alleles":["AAAAAAAA","AAAAAAAAA","AAAAAAAAAA"],"end":140437478,"clinical_significance":[],"seq_region_name":"7","id":"rs1328238092"},{"source":"dbSNP","start":140437478,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140437478,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799789161"},{"end":140437479,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140437479,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs901072422","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437479,"feature_type":"variation","strand":1,"end":140437479,"alleles":["C","-"],"clinical_significance":[],"seq_region_name":"7","id":"rs1425579896"},{"clinical_significance":[],"seq_region_name":"7","id":"rs79572427","alleles":["A","T"],"end":140437480,"feature_type":"variation","strand":1,"source":"dbSNP","start":140437480,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs78415979","end":140437482,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140437482,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"alleles":["TTTTTTTT","TTTTTTT","TTTTTTTTT"],"end":140437489,"feature_type":"variation","strand":1,"source":"dbSNP","start":140437482,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs200273192"},{"seq_region_name":"7","id":"rs112623527","clinical_significance":[],"end":140437488,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140437488,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799789338","end":140437488,"alleles":["-","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140437489,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"id":"rs11771680","seq_region_name":"7","clinical_significance":[],"start":140437489,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","A"],"end":140437489,"strand":1,"feature_type":"variation"},{"start":140437489,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140437490,"alleles":["TA","-"],"strand":1,"feature_type":"variation","id":"rs1799789436","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs191956392","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437490,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140437490},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799789515","alleles":["AAAAAA","AAAAA","AAAAAAA"],"end":140437495,"feature_type":"variation","strand":1,"source":"dbSNP","start":140437490,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140437494,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437494,"source":"dbSNP","seq_region_name":"7","id":"rs1563079640","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799789550","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437496,"source":"dbSNP","strand":1,"feature_type":"variation","end":140437496,"alleles":["G","A"]},{"end":140437498,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140437498,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs2130197642","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs979457822","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437500,"feature_type":"variation","strand":1,"end":140437500,"alleles":["A","G"]},{"clinical_significance":[],"id":"rs1799789587","seq_region_name":"7","feature_type":"variation","strand":1,"end":140437501,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437501},{"feature_type":"variation","strand":1,"end":140437502,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437502,"clinical_significance":[],"id":"rs111525920","seq_region_name":"7"},{"start":140437508,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140437508,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1278588682","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799789650","seq_region_name":"7","alleles":["A","G"],"end":140437512,"feature_type":"variation","strand":1,"source":"dbSNP","start":140437512,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1799789664","clinical_significance":[],"end":140437514,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140437514,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585445851","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437516,"feature_type":"variation","strand":1,"end":140437516,"alleles":["T","C","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799789702","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437524,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140437524},{"id":"rs1799789715","seq_region_name":"7","clinical_significance":[],"start":140437525,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140437525,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130197661","feature_type":"variation","strand":1,"end":140437527,"alleles":["A","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437527},{"seq_region_name":"7","id":"rs1799789734","clinical_significance":[],"end":140437528,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140437528,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140437535,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437535,"source":"dbSNP","id":"rs1031751343","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799789778","feature_type":"variation","strand":1,"end":140437537,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437537},{"end":140437538,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140437538,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799789800","clinical_significance":[]},{"source":"dbSNP","start":140437547,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140437547,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799789830"},{"feature_type":"variation","strand":1,"end":140437548,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437548,"clinical_significance":[],"seq_region_name":"7","id":"rs1313044485"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1032721836","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140437550,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437550},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140437554,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437554,"source":"dbSNP","seq_region_name":"7","id":"rs1799789895","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs956234089","alleles":["C","T"],"end":140437555,"feature_type":"variation","strand":1,"source":"dbSNP","start":140437555,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"end":140437563,"alleles":["AATA","-"],"strand":1,"feature_type":"variation","start":140437560,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1205301942","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799789974","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140437561,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437561,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs956731346","source":"dbSNP","start":140437563,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140437563,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140437565,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437565,"clinical_significance":[],"id":"rs988249882","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140437572,"alleles":["CAGTCCA","CA"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437566,"clinical_significance":[],"seq_region_name":"7","id":"rs1799790043"},{"clinical_significance":[],"seq_region_name":"7","id":"rs748845207","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437577,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140437577},{"alleles":["T","G"],"end":140437581,"strand":1,"feature_type":"variation","start":140437581,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs780039164","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140437590,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["TTACTT","TT"],"end":140437595,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1208044627","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140437592,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437592,"source":"dbSNP","id":"rs1799790158","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140437593,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140437593,"alleles":["C","CC"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs980481101"},{"feature_type":"variation","strand":1,"end":140437593,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437593,"clinical_significance":[],"id":"rs1799790180","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["-","AT"],"end":140437593,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437594,"source":"dbSNP","seq_region_name":"7","id":"rs1799790243","clinical_significance":[]},{"source":"dbSNP","start":140437594,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140437602,"alleles":["TTTTTTTTT","TTTTTTTT","TTTTTTTTTT","TTTTTTTTTTT","TTTTTTTTTTTTTTTTT"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs11424844"},{"id":"rs1799790357","seq_region_name":"7","clinical_significance":[],"start":140437595,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","A"],"end":140437595,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs926244174","feature_type":"variation","strand":1,"end":140437595,"alleles":["-","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437596},{"clinical_significance":[],"seq_region_name":"7","id":"rs1428428510","feature_type":"variation","strand":1,"end":140437596,"alleles":["T","C","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437596},{"id":"rs1171333071","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140437598,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437598,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1430329304","alleles":["T","C"],"end":140437600,"feature_type":"variation","strand":1,"source":"dbSNP","start":140437600,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1259713095","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437601,"feature_type":"variation","strand":1,"end":140437601,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1799790496","clinical_significance":[],"start":140437601,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140437605,"alleles":["TTCTT","TT"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs552101868","clinical_significance":[],"strand":1,"feature_type":"variation","end":140437603,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437603,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799790559","alleles":["TTTTTT","TT"],"end":140437609,"feature_type":"variation","strand":1,"source":"dbSNP","start":140437604,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437610,"source":"dbSNP","strand":1,"feature_type":"variation","end":140437610,"alleles":["G","T"],"seq_region_name":"7","id":"rs1191569946","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437610,"feature_type":"variation","strand":1,"alleles":["GAGGTGG","-"],"end":140437616,"clinical_significance":[],"seq_region_name":"7","id":"rs1799790683"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437611,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140437611,"clinical_significance":[],"id":"rs1799790713","seq_region_name":"7"},{"id":"rs1159300669","seq_region_name":"7","clinical_significance":[],"start":140437616,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","T"],"end":140437616,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1293888948","feature_type":"variation","strand":1,"end":140437623,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437623},{"source":"dbSNP","start":140437624,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140437624,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799790801"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799790824","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437625,"feature_type":"variation","strand":1,"alleles":["TT","T"],"end":140437626},{"seq_region_name":"7","id":"rs931074054","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140437626,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437626,"source":"dbSNP"},{"source":"dbSNP","start":140437627,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140437627,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1387255160"},{"start":140437628,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140437628,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799790905","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1048169662","feature_type":"variation","strand":1,"end":140437629,"alleles":["T","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437629},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799790957","source":"dbSNP","start":140437639,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140437639,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1319964150","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437640,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140437640},{"alleles":["C","G"],"end":140437645,"feature_type":"variation","strand":1,"source":"dbSNP","start":140437645,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799790997"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140437647,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437647,"clinical_significance":[],"id":"rs908281328","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799791033","clinical_significance":[],"start":140437648,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140437648,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"end":140437649,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140437649,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799791057"},{"clinical_significance":[],"seq_region_name":"7","id":"rs939885948","feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140437653,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437653},{"seq_region_name":"7","id":"rs747101036","clinical_significance":[],"alleles":["G","A","C","T"],"end":140437654,"strand":1,"feature_type":"variation","start":140437654,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140437655,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437655,"clinical_significance":[],"seq_region_name":"7","id":"rs1799791289"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437656,"feature_type":"variation","strand":1,"end":140437656,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs570940813"},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140437665,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437665,"source":"dbSNP","seq_region_name":"7","id":"rs1585445942","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585445946","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437671,"source":"dbSNP","strand":1,"feature_type":"variation","end":140437671,"alleles":["A","C"]},{"start":140437672,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140437672,"alleles":["C","A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1037949694","clinical_significance":[]},{"clinical_significance":[],"id":"rs1450133903","seq_region_name":"7","source":"dbSNP","start":140437676,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140437676,"feature_type":"variation","strand":1},{"alleles":["G","A"],"end":140437677,"feature_type":"variation","strand":1,"source":"dbSNP","start":140437677,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs918956387"},{"end":140437679,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140437679,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs928954520"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1463461870","feature_type":"variation","strand":1,"end":140437680,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437680},{"id":"rs1051488332","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140437684,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437684,"source":"dbSNP"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437686,"feature_type":"variation","strand":1,"end":140437686,"alleles":["G","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs890174562"},{"end":140437687,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140437687,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1585445970","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437694,"feature_type":"variation","strand":1,"end":140437694,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799791518"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1007363756","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437695,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140437695},{"seq_region_name":"7","id":"rs1799791554","clinical_significance":[],"start":140437696,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140437696,"strand":1,"feature_type":"variation"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437697,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140437697,"clinical_significance":[],"id":"rs1182004519","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1239321407","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437698,"feature_type":"variation","strand":1,"end":140437698,"alleles":["T","C","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1049758709","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140437703,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437703},{"seq_region_name":"7","id":"rs1799791654","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437710,"source":"dbSNP","strand":1,"feature_type":"variation","end":140437710,"alleles":["C","T"]},{"start":140437714,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140437714,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1280867253","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437715,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140437715,"seq_region_name":"7","id":"rs1239139174","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1348083986","feature_type":"variation","strand":1,"end":140437716,"alleles":["G","A","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437716},{"seq_region_name":"7","id":"rs1479936281","clinical_significance":[],"alleles":["A","G"],"end":140437720,"strand":1,"feature_type":"variation","start":140437720,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"alleles":["A","C"],"end":140437732,"strand":1,"feature_type":"variation","start":140437732,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799791766","clinical_significance":[]},{"seq_region_name":"7","id":"rs1039237250","clinical_significance":[],"alleles":["C","A","T"],"end":140437735,"strand":1,"feature_type":"variation","start":140437735,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"source":"dbSNP","start":140437739,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140437739,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799791812","seq_region_name":"7"},{"alleles":["A","T"],"end":140437740,"feature_type":"variation","strand":1,"source":"dbSNP","start":140437740,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585445994"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140437741,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437741,"source":"dbSNP","seq_region_name":"7","id":"rs1251254629","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs59860195","source":"dbSNP","start":140437744,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140437744,"alleles":["A","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs904445584","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437745,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140437745},{"id":"rs538369137","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140437747,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437747,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1359568576","feature_type":"variation","strand":1,"end":140437748,"alleles":["G","A","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437748},{"seq_region_name":"7","id":"rs1799791963","clinical_significance":[],"strand":1,"feature_type":"variation","end":140437750,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437750,"source":"dbSNP"},{"seq_region_name":"7","id":"rs537005484","clinical_significance":[],"start":140437751,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140437751,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs904557507","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437752,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140437752},{"clinical_significance":[],"id":"rs1799792047","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437753,"feature_type":"variation","strand":1,"end":140437753,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799792066","alleles":["C","T"],"end":140437754,"feature_type":"variation","strand":1,"source":"dbSNP","start":140437754,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs956951737","clinical_significance":[],"strand":1,"feature_type":"variation","end":140437756,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437756,"source":"dbSNP"},{"seq_region_name":"7","id":"rs2130197984","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140437762,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437762,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1392937659","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140437766,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437766},{"strand":1,"feature_type":"variation","end":140437780,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437780,"source":"dbSNP","seq_region_name":"7","id":"rs556591955","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs574924717","feature_type":"variation","strand":1,"end":140437781,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437781},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437784,"source":"dbSNP","strand":1,"feature_type":"variation","end":140437784,"alleles":["T","G"],"seq_region_name":"7","id":"rs1799792176","clinical_significance":[]},{"source":"dbSNP","start":140437785,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140437785,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799792203"},{"alleles":["G","A"],"end":140437796,"strand":1,"feature_type":"variation","start":140437796,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs2130198004","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140437800,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140437800,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799792230","seq_region_name":"7"},{"clinical_significance":[],"id":"rs376794463","seq_region_name":"7","alleles":["G","A","T"],"end":140437801,"feature_type":"variation","strand":1,"source":"dbSNP","start":140437801,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437802,"feature_type":"variation","strand":1,"end":140437802,"alleles":["C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799792279"},{"start":140437806,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","A","G"],"end":140437806,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1367507882","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437809,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140437809,"seq_region_name":"7","id":"rs1585446031","clinical_significance":[]},{"clinical_significance":[],"id":"rs769718939","seq_region_name":"7","end":140437810,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140437810,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"id":"rs1799792387","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140437813,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437813,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1799792419","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437815,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140437815},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140437828,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437828,"source":"dbSNP","seq_region_name":"7","id":"rs1799792442","clinical_significance":[]},{"seq_region_name":"7","id":"rs182923670","clinical_significance":[],"strand":1,"feature_type":"variation","end":140437832,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437832,"source":"dbSNP"},{"alleles":["C","A"],"end":140437833,"strand":1,"feature_type":"variation","start":140437833,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799792463","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437836,"source":"dbSNP","strand":1,"feature_type":"variation","end":140437836,"alleles":["C","T"],"seq_region_name":"7","id":"rs1417708122","clinical_significance":[]},{"seq_region_name":"7","id":"rs1014444144","clinical_significance":[],"start":140437839,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140437839,"strand":1,"feature_type":"variation"},{"id":"rs1210980207","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140437842,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437842,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["G","C","T"],"end":140437858,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437858,"clinical_significance":[],"id":"rs1490996599","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1183709381","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437860,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140437860},{"end":140437862,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140437862,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799792585"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437863,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140437863,"seq_region_name":"7","id":"rs1219697117","clinical_significance":[]},{"start":140437866,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A","C"],"end":140437866,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs980943723","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799792659","source":"dbSNP","start":140437868,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140437868,"alleles":["G","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1585446061","clinical_significance":[],"strand":1,"feature_type":"variation","end":140437869,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437869,"source":"dbSNP"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437870,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140437870,"clinical_significance":[],"id":"rs1365838010","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140437873,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437873,"source":"dbSNP","id":"rs868201386","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1158581028","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140437876,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437876,"source":"dbSNP"},{"source":"dbSNP","start":140437877,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140437877,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799792764"},{"start":140437878,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140437878,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799792795","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799792852","clinical_significance":[],"start":140437880,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140437880,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs554395246","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437883,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140437883},{"start":140437884,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140437884,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs963575322","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799792921","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437886,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140437886},{"clinical_significance":[],"id":"rs974085624","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140437890,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437890},{"feature_type":"variation","strand":1,"end":140437891,"alleles":["A","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437891,"clinical_significance":[],"seq_region_name":"7","id":"rs572674210"},{"strand":1,"feature_type":"variation","end":140437895,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437895,"source":"dbSNP","seq_region_name":"7","id":"rs546346875","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799793026","source":"dbSNP","start":140437896,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140437896,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140437897,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437897,"source":"dbSNP","seq_region_name":"7","id":"rs1799793051","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799793076","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437899,"feature_type":"variation","strand":1,"end":140437899,"alleles":["A","G"]},{"clinical_significance":[],"id":"rs1585446085","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437901,"feature_type":"variation","strand":1,"end":140437901,"alleles":["T","A"]},{"clinical_significance":[],"id":"rs952403214","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437902,"feature_type":"variation","strand":1,"end":140437902,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1392393082","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437902,"feature_type":"variation","strand":1,"alleles":["AAAACAAAAACAAAAACAAAAA","AAAACAAAAA","AAAACAAAAACAAAAA","AAAACAAAAACAAAAACAAAAACAAAAA"],"end":140437923},{"seq_region_name":"7","id":"rs1160544681","clinical_significance":[],"start":140437904,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","T"],"end":140437904,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1331257065","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","-"],"end":140437912,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437912,"source":"dbSNP"},{"alleles":["C","A"],"end":140437912,"strand":1,"feature_type":"variation","start":140437912,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1333673115","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140437913,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437913,"clinical_significance":[],"seq_region_name":"7","id":"rs928987074"},{"strand":1,"feature_type":"variation","alleles":["AAAAA","AAAAAA"],"end":140437917,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437913,"source":"dbSNP","seq_region_name":"7","id":"rs1799793317","clinical_significance":[]},{"seq_region_name":"7","id":"rs1200068382","clinical_significance":[],"end":140437928,"alleles":["AAAAACAAAAAAAAAA","AAA"],"strand":1,"feature_type":"variation","start":140437913,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1363559446","clinical_significance":[],"start":140437913,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["AAAAACAAAAAAAAAACAA","AAAAACAA"],"end":140437931,"strand":1,"feature_type":"variation"},{"end":140437916,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140437916,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1293410422"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1196568794","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437917,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140437917},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437918,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140437918,"id":"rs1490053339","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs201639077","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437919,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AAAAAAAAAA","AAA","AAAAAAAA","AAAAAAAAA","AAAAAAAAAAA","AAAAAAAAAAAA"],"end":140437928},{"clinical_significance":[],"id":"rs1799793544","seq_region_name":"7","feature_type":"variation","strand":1,"end":140437921,"alleles":["A","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437921},{"seq_region_name":"7","id":"rs1348151971","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437922,"source":"dbSNP","strand":1,"feature_type":"variation","end":140437922,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs187554968","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437924,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140437924},{"seq_region_name":"7","id":"rs1799793635","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437925,"source":"dbSNP","strand":1,"feature_type":"variation","end":140437925,"alleles":["A","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs576510697","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140437926,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437926},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437927,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140437927,"id":"rs911642266","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140437927,"alleles":["-","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437928,"clinical_significance":[],"seq_region_name":"7","id":"rs1799793686"},{"source":"dbSNP","start":140437928,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140437928,"alleles":["A","C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs943087624","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437928,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["ACA","A"],"end":140437930,"seq_region_name":"7","id":"rs1231396311","clinical_significance":[]},{"start":140437929,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140437929,"alleles":["C","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs543950364","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","-"],"end":140437929,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437929,"clinical_significance":[],"id":"rs1799793792","seq_region_name":"7"},{"alleles":["A","G"],"end":140437931,"feature_type":"variation","strand":1,"source":"dbSNP","start":140437931,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1197375051"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1380709593","source":"dbSNP","start":140437933,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140437933,"alleles":["A","G"],"feature_type":"variation","strand":1},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437933,"feature_type":"variation","strand":1,"end":140437935,"alleles":["AGA","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs932493293"},{"end":140437933,"alleles":["-","CAT"],"strand":1,"feature_type":"variation","start":140437934,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1799793888","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1384603598","end":140437934,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140437934,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1050146234","clinical_significance":[],"start":140437939,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140437939,"strand":1,"feature_type":"variation"},{"end":140437946,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140437946,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1471165720"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140437947,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437947,"clinical_significance":[],"id":"rs1799793944","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1585446162","clinical_significance":[],"strand":1,"feature_type":"variation","end":140437953,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437953,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437954,"source":"dbSNP","strand":1,"feature_type":"variation","end":140437954,"alleles":["C","G"],"seq_region_name":"7","id":"rs1585446166","clinical_significance":[]},{"seq_region_name":"7","id":"rs1427770661","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437963,"source":"dbSNP","strand":1,"feature_type":"variation","end":140437963,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs571104169","end":140437964,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140437964,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["AGGAGG","AGG"],"end":140437969,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437964,"source":"dbSNP","seq_region_name":"7","id":"rs1799794054","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799794086","source":"dbSNP","start":140437966,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140437966,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs2130198233","clinical_significance":[],"start":140437968,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140437968,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799794105","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140437970,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437970},{"clinical_significance":[],"id":"rs1176368295","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437971,"feature_type":"variation","strand":1,"end":140437971,"alleles":["T","-"]},{"feature_type":"variation","strand":1,"end":140437972,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140437972,"clinical_significance":[],"id":"rs1799794150","seq_region_name":"7"},{"alleles":["G","A"],"end":140437974,"strand":1,"feature_type":"variation","start":140437974,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1476056466","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799794196","clinical_significance":[],"end":140437975,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140437975,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"strand":1,"feature_type":"variation","end":140437976,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437976,"source":"dbSNP","seq_region_name":"7","id":"rs1799794216","clinical_significance":[]},{"alleles":["A","T"],"end":140437977,"strand":1,"feature_type":"variation","start":140437977,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1482208109","clinical_significance":[]},{"alleles":["T","C"],"end":140437985,"feature_type":"variation","strand":1,"source":"dbSNP","start":140437985,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1258319361"},{"strand":1,"feature_type":"variation","end":140437986,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437986,"source":"dbSNP","seq_region_name":"7","id":"rs1476194276","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585446177","source":"dbSNP","start":140437992,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140437992,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799794337","source":"dbSNP","start":140437994,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140437994,"alleles":["C","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1799794364","clinical_significance":[],"end":140437995,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140437995,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"strand":1,"feature_type":"variation","end":140437996,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140437996,"source":"dbSNP","seq_region_name":"7","id":"rs1194783140","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130198276","clinical_significance":[],"start":140437996,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140437996,"alleles":["A","AA"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799794407","end":140437997,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140437997,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130198283","alleles":["G","A"],"end":140438006,"feature_type":"variation","strand":1,"source":"dbSNP","start":140438006,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"end":140438009,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140438009,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799794427"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438010,"source":"dbSNP","strand":1,"feature_type":"variation","end":140438010,"alleles":["G","T"],"id":"rs1799794449","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140438012,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140438012,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1162755395"},{"source":"dbSNP","start":140438017,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140438017,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1368463524"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438018,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140438018,"seq_region_name":"7","id":"rs193297719","clinical_significance":[]},{"seq_region_name":"7","id":"rs1203989601","clinical_significance":[],"start":140438019,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140438019,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438020,"source":"dbSNP","strand":1,"feature_type":"variation","end":140438020,"alleles":["A","G"],"seq_region_name":"7","id":"rs2130198307","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130198310","clinical_significance":[],"alleles":["A","G"],"end":140438026,"strand":1,"feature_type":"variation","start":140438026,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"id":"rs1462925513","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140438027,"alleles":["T","A","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438027,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1261122665","seq_region_name":"7","feature_type":"variation","strand":1,"end":140438028,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438028},{"start":140438028,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140438028,"alleles":["G","-"],"strand":1,"feature_type":"variation","id":"rs1799794604","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799794621","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140438032,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438032},{"seq_region_name":"7","id":"rs1222797429","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438036,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140438036},{"start":140438044,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140438044,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799794658","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs768122586","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438045,"feature_type":"variation","strand":1,"end":140438045,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130198337","source":"dbSNP","start":140438048,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140438048,"alleles":["G","A"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438048,"source":"dbSNP","strand":1,"feature_type":"variation","end":140438050,"alleles":["GTG","G"],"seq_region_name":"7","id":"rs1585446203","clinical_significance":[]},{"alleles":["T","C"],"end":140438049,"strand":1,"feature_type":"variation","start":140438049,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1585446205","clinical_significance":[]},{"id":"rs2130198350","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438051,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["-","A"],"end":140438050},{"clinical_significance":[],"seq_region_name":"7","id":"rs1340034605","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438051,"feature_type":"variation","strand":1,"end":140438051,"alleles":["C","A"]},{"feature_type":"variation","strand":1,"alleles":["-","A"],"end":140438051,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438052,"clinical_significance":[],"id":"rs1170031742","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1369055537","clinical_significance":[],"alleles":["T","A"],"end":140438052,"strand":1,"feature_type":"variation","start":140438052,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"id":"rs1799794808","seq_region_name":"7","clinical_significance":[],"end":140438053,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140438053,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130198364","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438053,"feature_type":"variation","strand":1,"alleles":["GG","G"],"end":140438054},{"seq_region_name":"7","id":"rs1408845501","clinical_significance":[],"alleles":["-","A"],"end":140438053,"strand":1,"feature_type":"variation","start":140438054,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"end":140438054,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140438054,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799794855"},{"alleles":["A","G","T"],"end":140438055,"feature_type":"variation","strand":1,"source":"dbSNP","start":140438055,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799794884"},{"source":"dbSNP","start":140438056,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140438056,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1313049824"},{"id":"rs1799794926","seq_region_name":"7","clinical_significance":[],"start":140438058,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140438058,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438060,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140438060,"id":"rs1356964817","seq_region_name":"7","clinical_significance":[]},{"id":"rs529651509","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438061,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140438061},{"source":"dbSNP","start":140438062,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["CTCT","CT"],"end":140438065,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799794998","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs904423744","end":140438063,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140438063,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"alleles":["T","C"],"end":140438065,"strand":1,"feature_type":"variation","start":140438065,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799795045","clinical_significance":[]},{"seq_region_name":"7","id":"rs541464723","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A","G"],"end":140438069,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438069,"source":"dbSNP"},{"source":"dbSNP","start":140438071,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140438076,"alleles":["AAAAAA","AAAAAAATAAAAAAA"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130198401"},{"alleles":["A","C"],"end":140438076,"feature_type":"variation","strand":1,"source":"dbSNP","start":140438076,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs770607697"},{"clinical_significance":[],"seq_region_name":"7","id":"rs560360901","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438077,"feature_type":"variation","strand":1,"end":140438077,"alleles":["G","A"]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438077,"feature_type":"variation","strand":1,"end":140438079,"alleles":["GGG","-"],"clinical_significance":[],"id":"rs2130198414","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs527623803","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438078,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140438078},{"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140438080,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438080,"clinical_significance":[],"seq_region_name":"7","id":"rs1585446232"},{"seq_region_name":"7","id":"rs2130198430","clinical_significance":[],"end":140438082,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140438082,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"end":140438087,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140438087,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1336531039"},{"id":"rs1053079811","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140438089,"strand":1,"feature_type":"variation","start":140438089,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"id":"rs184303936","seq_region_name":"7","feature_type":"variation","strand":1,"end":140438090,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438090},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438091,"feature_type":"variation","strand":1,"end":140438091,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1169084753"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1474142777","alleles":["C","T"],"end":140438093,"feature_type":"variation","strand":1,"source":"dbSNP","start":140438093,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1799795332","clinical_significance":[],"strand":1,"feature_type":"variation","end":140438094,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438094,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1799795356","seq_region_name":"7","source":"dbSNP","start":140438096,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140438096,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140438099,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438099,"clinical_significance":[],"seq_region_name":"7","id":"rs1389124269"},{"start":140438106,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G","T"],"end":140438106,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130198451","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1183846381","end":140438109,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140438109,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"start":140438118,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","T"],"end":140438118,"strand":1,"feature_type":"variation","id":"rs1341111625","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438120,"source":"dbSNP","strand":1,"feature_type":"variation","end":140438120,"alleles":["C","A"],"seq_region_name":"7","id":"rs1799795435","clinical_significance":[]},{"id":"rs1799795462","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140438121,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438121,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1204719058","clinical_significance":[],"start":140438122,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140438122,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130198471","alleles":["T","A"],"end":140438124,"feature_type":"variation","strand":1,"source":"dbSNP","start":140438124,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1799795510","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140438125,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438125,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1446130441","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438127,"feature_type":"variation","strand":1,"end":140438127,"alleles":["G","A"]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438128,"source":"dbSNP","strand":1,"feature_type":"variation","end":140438128,"alleles":["G","A"],"seq_region_name":"7","id":"rs1240999741","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1281382494","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140438130,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438130},{"clinical_significance":[],"seq_region_name":"7","id":"rs1486773687","source":"dbSNP","start":140438133,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140438133,"alleles":["T","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1413052648","end":140438136,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140438136,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799795624","feature_type":"variation","strand":1,"end":140438137,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438137},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438138,"feature_type":"variation","strand":1,"end":140438138,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1180233056"},{"alleles":["C","T"],"end":140438142,"feature_type":"variation","strand":1,"source":"dbSNP","start":140438142,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1255499321"},{"start":140438143,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140438143,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1429663033","clinical_significance":[]},{"id":"rs1195873683","seq_region_name":"7","clinical_significance":[],"end":140438144,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140438144,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140438149,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438149,"source":"dbSNP","seq_region_name":"7","id":"rs1388723358","clinical_significance":[]},{"end":140438152,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140438152,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1429583931","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140438153,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438153,"source":"dbSNP","id":"rs1799795806","seq_region_name":"7","clinical_significance":[]},{"id":"rs1248410040","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438157,"source":"dbSNP","strand":1,"feature_type":"variation","end":140438157,"alleles":["G","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1174655918","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438160,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140438160},{"clinical_significance":[],"seq_region_name":"7","id":"rs1376946339","source":"dbSNP","start":140438162,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140438162,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1014717689","seq_region_name":"7","alleles":["C","G","T"],"end":140438163,"feature_type":"variation","strand":1,"source":"dbSNP","start":140438163,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"end":140438164,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140438164,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1356718415","clinical_significance":[]},{"source":"dbSNP","start":140438167,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140438167,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585446297"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438168,"feature_type":"variation","strand":1,"end":140438168,"alleles":["C","G"],"clinical_significance":[],"id":"rs1327469615","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs570705967","feature_type":"variation","strand":1,"end":140438169,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438169},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438170,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140438170,"clinical_significance":[],"seq_region_name":"7","id":"rs970666393"},{"start":140438171,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","G"],"end":140438171,"strand":1,"feature_type":"variation","id":"rs369627211","seq_region_name":"7","clinical_significance":[]},{"end":140438173,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140438173,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1446073843","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140438174,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438174,"source":"dbSNP","seq_region_name":"7","id":"rs1799796114","clinical_significance":[]},{"end":140438175,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140438175,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799796137"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438179,"source":"dbSNP","strand":1,"feature_type":"variation","end":140438179,"alleles":["A","G"],"id":"rs189582610","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438181,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140438181,"clinical_significance":[],"id":"rs568567413","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1470409490","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438183,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140438183},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438184,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140438184,"seq_region_name":"7","id":"rs1234489424","clinical_significance":[]},{"start":140438184,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["GG","G"],"end":140438185,"strand":1,"feature_type":"variation","id":"rs1799796271","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1179550293","feature_type":"variation","strand":1,"end":140438191,"alleles":["C","A","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438191},{"seq_region_name":"7","id":"rs1585446323","clinical_significance":[],"start":140438191,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["CCCC","CC","CCC"],"end":140438194,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1292584840","clinical_significance":[],"end":140438194,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140438194,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs13307868","clinical_significance":[],"start":140438195,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140438195,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1799796392","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140438197,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438197},{"clinical_significance":[],"id":"rs1224894531","seq_region_name":"7","source":"dbSNP","start":140438203,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140438203,"alleles":["T","C"],"feature_type":"variation","strand":1},{"start":140438204,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140438204,"strand":1,"feature_type":"variation","id":"rs1295236663","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs952266744","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140438208,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438208,"source":"dbSNP"},{"seq_region_name":"7","id":"rs2130198615","clinical_significance":[],"strand":1,"feature_type":"variation","end":140438209,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438209,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799796497","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438211,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140438211},{"start":140438212,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["-","GA","GAA","GAAA","GAAAAA","GAAAAAAA","GAAAAAAAA"],"end":140438211,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1450666274","clinical_significance":[]},{"seq_region_name":"7","id":"rs1364352785","clinical_significance":[],"start":140438212,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140438212,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs13308963","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438215,"feature_type":"variation","strand":1,"end":140438215,"alleles":["A","T"]},{"seq_region_name":"7","id":"rs1234836195","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140438217,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438217,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1305317379","alleles":["T","A","G"],"end":140438218,"feature_type":"variation","strand":1,"source":"dbSNP","start":140438218,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140438220,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140438220,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs983767977"},{"alleles":["C","T"],"end":140438222,"strand":1,"feature_type":"variation","start":140438222,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs535810649","clinical_significance":[]},{"clinical_significance":[],"id":"rs1350351180","seq_region_name":"7","source":"dbSNP","start":140438223,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140438223,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1799796731","seq_region_name":"7","alleles":["G","A"],"end":140438224,"feature_type":"variation","strand":1,"source":"dbSNP","start":140438224,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438236,"source":"dbSNP","strand":1,"feature_type":"variation","end":140438236,"alleles":["A","G"],"seq_region_name":"7","id":"rs1799796744","clinical_significance":[]},{"source":"dbSNP","start":140438236,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140438236,"alleles":["A","AA"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799796763"},{"id":"rs1799796790","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140438237,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438237,"source":"dbSNP"},{"start":140438238,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140438238,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799796816","clinical_significance":[]},{"seq_region_name":"7","id":"rs553897421","clinical_significance":[],"strand":1,"feature_type":"variation","end":140438239,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438239,"source":"dbSNP"},{"alleles":["G","A"],"end":140438240,"strand":1,"feature_type":"variation","start":140438240,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1303211791","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799796886","clinical_significance":[],"alleles":["T","G"],"end":140438243,"strand":1,"feature_type":"variation","start":140438243,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1426014385","end":140438246,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140438246,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"start":140438247,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140438247,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130198681","clinical_significance":[]},{"seq_region_name":"7","id":"rs1363291646","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438249,"source":"dbSNP","strand":1,"feature_type":"variation","end":140438249,"alleles":["C","T"]},{"start":140438250,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140438250,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585446369","clinical_significance":[]},{"alleles":["A","G"],"end":140438252,"feature_type":"variation","strand":1,"source":"dbSNP","start":140438252,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799796960"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799796979","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438256,"feature_type":"variation","strand":1,"end":140438256,"alleles":["A","C"]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438259,"source":"dbSNP","strand":1,"feature_type":"variation","end":140438259,"alleles":["C","G","T"],"seq_region_name":"7","id":"rs1163665531","clinical_significance":[]},{"id":"rs1799797024","seq_region_name":"7","clinical_significance":[],"alleles":["G","C"],"end":140438261,"strand":1,"feature_type":"variation","start":140438261,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1585446372","clinical_significance":[],"start":140438262,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140438262,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799797062","alleles":["A","G"],"end":140438263,"feature_type":"variation","strand":1,"source":"dbSNP","start":140438263,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1400984477","clinical_significance":[],"alleles":["G","A"],"end":140438268,"strand":1,"feature_type":"variation","start":140438268,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1409853519","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438271,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140438271},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130198711","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438272,"feature_type":"variation","strand":1,"end":140438272,"alleles":["A","C"]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438275,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140438275,"seq_region_name":"7","id":"rs1799797130","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1156665554","source":"dbSNP","start":140438276,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140438276,"alleles":["A","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585446377","alleles":["G","C"],"end":140438277,"feature_type":"variation","strand":1,"source":"dbSNP","start":140438277,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"start":140438279,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140438279,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799797193","clinical_significance":[]},{"start":140438280,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140438280,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs761392695","clinical_significance":[]},{"start":140438281,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140438281,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs192627643","clinical_significance":[]},{"seq_region_name":"7","id":"rs1255496215","clinical_significance":[],"strand":1,"feature_type":"variation","end":140438282,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438282,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799797306","clinical_significance":[],"strand":1,"feature_type":"variation","end":140438284,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438284,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1489888822","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140438289,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438289},{"strand":1,"feature_type":"variation","end":140438293,"alleles":["AA","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438292,"source":"dbSNP","seq_region_name":"7","id":"rs1486203191","clinical_significance":[]},{"seq_region_name":"7","id":"rs373263548","clinical_significance":[],"end":140438297,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140438297,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs961118588","alleles":["C","T"],"end":140438299,"feature_type":"variation","strand":1,"source":"dbSNP","start":140438299,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"end":140438300,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140438300,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1799797430","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs976942558","seq_region_name":"7","source":"dbSNP","start":140438303,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140438303,"feature_type":"variation","strand":1},{"start":140438304,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140438304,"alleles":["G","C"],"strand":1,"feature_type":"variation","id":"rs1799797474","seq_region_name":"7","clinical_significance":[]},{"id":"rs1282588189","seq_region_name":"7","clinical_significance":[],"start":140438305,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140438305,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799797500","end":140438307,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140438307,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140438314,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140438314,"alleles":["C","A","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1246800634"},{"start":140438315,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140438315,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1324821695","clinical_significance":[]},{"seq_region_name":"7","id":"rs1285754379","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438316,"source":"dbSNP","strand":1,"feature_type":"variation","end":140438316,"alleles":["C","G"]},{"seq_region_name":"7","id":"rs1165097987","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140438317,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438317,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799797632","alleles":["C","G"],"end":140438322,"feature_type":"variation","strand":1,"source":"dbSNP","start":140438322,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140438323,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438323,"source":"dbSNP","seq_region_name":"7","id":"rs1449364966","clinical_significance":[]},{"end":140438324,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140438324,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1194713940"},{"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140438325,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438325,"source":"dbSNP","seq_region_name":"7","id":"rs557929488","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438326,"feature_type":"variation","strand":1,"end":140438326,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs576270593"},{"seq_region_name":"7","id":"rs1585446419","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140438328,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438328,"source":"dbSNP"},{"seq_region_name":"7","id":"rs922372484","clinical_significance":[],"start":140438331,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140438331,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140438333,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438333,"clinical_significance":[],"id":"rs1799797793","seq_region_name":"7"},{"id":"rs1799797813","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140438334,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438334,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140438341,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438341,"source":"dbSNP","seq_region_name":"7","id":"rs1799797833","clinical_significance":[]},{"id":"rs1799797854","seq_region_name":"7","clinical_significance":[],"start":140438342,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C","G"],"end":140438342,"strand":1,"feature_type":"variation"},{"alleles":["-","TGA"],"end":140438345,"strand":1,"feature_type":"variation","start":140438346,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799797886","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140438346,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438346,"source":"dbSNP","seq_region_name":"7","id":"rs1799797902","clinical_significance":[]},{"start":140438346,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["CA","-"],"end":140438347,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1431122478","clinical_significance":[]},{"seq_region_name":"7","id":"rs1174833783","clinical_significance":[],"end":140438347,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140438347,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"id":"rs1345281627","seq_region_name":"7","clinical_significance":[],"start":140438348,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140438348,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1454945814","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438351,"feature_type":"variation","strand":1,"alleles":["-","CT"],"end":140438350},{"start":140438351,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","C"],"end":140438351,"strand":1,"feature_type":"variation","id":"rs1346657602","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1317950143","clinical_significance":[],"alleles":["A","T"],"end":140438352,"strand":1,"feature_type":"variation","start":140438352,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1156597593","clinical_significance":[],"end":140438354,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140438354,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140438357,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438357,"clinical_significance":[],"seq_region_name":"7","id":"rs1387867615"},{"strand":1,"feature_type":"variation","end":140438358,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438358,"source":"dbSNP","seq_region_name":"7","id":"rs1429863140","clinical_significance":[]},{"end":140438362,"alleles":["CTCT","CT"],"strand":1,"feature_type":"variation","start":140438359,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1178527054","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140438360,"alleles":["T","A","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438360,"source":"dbSNP","seq_region_name":"7","id":"rs867018519","clinical_significance":[]},{"source":"dbSNP","start":140438362,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140438362,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1441518132","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140438363,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438363,"clinical_significance":[],"seq_region_name":"7","id":"rs2130198862"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1327705823","feature_type":"variation","strand":1,"end":140438365,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438365},{"alleles":["G","A","T"],"end":140438366,"feature_type":"variation","strand":1,"source":"dbSNP","start":140438366,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1227938592","seq_region_name":"7"},{"source":"dbSNP","start":140438367,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["-","A"],"end":140438366,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799798231"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1240589049","end":140438367,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140438367,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140438367,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","-"],"end":140438367,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1486962092"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799798303","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438367,"feature_type":"variation","strand":1,"end":140438368,"alleles":["CA","-"]},{"start":140438368,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140438367,"alleles":["-","G"],"strand":1,"feature_type":"variation","id":"rs1799798323","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1365142999","end":140438368,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140438368,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["AAAAAAAAAAAAAAAAA","AAAAAAAA","AAAAAAAAAAA","AAAAAAAAAAAA","AAAAAAAAAAAAA","AAAAAAAAAAAAAA","AAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAA"],"end":140438384,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438368,"source":"dbSNP","id":"rs371805974","seq_region_name":"7","clinical_significance":[]},{"end":140438374,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140438374,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1363553175","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140438375,"alleles":["A","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438375,"clinical_significance":[],"seq_region_name":"7","id":"rs1300914583"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140438383,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438383,"source":"dbSNP","seq_region_name":"7","id":"rs1286789745","clinical_significance":[]},{"alleles":["A","T"],"end":140438384,"feature_type":"variation","strand":1,"source":"dbSNP","start":140438384,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130198926"},{"seq_region_name":"7","id":"rs1799798509","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438384,"source":"dbSNP","strand":1,"feature_type":"variation","end":140438385,"alleles":["AG","-"]},{"seq_region_name":"7","id":"rs1317736569","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438384,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AGGAGG","AGG"],"end":140438389},{"source":"dbSNP","start":140438385,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140438385,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799798557"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1230350207","end":140438386,"alleles":["GG","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140438385,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140438386,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438386,"clinical_significance":[],"seq_region_name":"7","id":"rs1799798611"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438387,"feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140438387,"clinical_significance":[],"seq_region_name":"7","id":"rs1266288691"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1464862143","source":"dbSNP","start":140438391,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140438391,"alleles":["C","G","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1799798681","clinical_significance":[],"end":140438393,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140438393,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1214824807","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438393,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GGCGCGGTGGC","GGC"],"end":140438403},{"clinical_significance":[],"seq_region_name":"7","id":"rs1255293978","end":140438395,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140438395,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1487678345","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140438396,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438396,"source":"dbSNP"},{"seq_region_name":"7","id":"rs771691198","clinical_significance":[],"start":140438397,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140438397,"strand":1,"feature_type":"variation"},{"end":140438398,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140438398,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1188145407","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438400,"source":"dbSNP","strand":1,"feature_type":"variation","end":140438400,"alleles":["T","G"],"seq_region_name":"7","id":"rs998981789","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799805057","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438400,"feature_type":"variation","strand":1,"end":140438404,"alleles":["TGGCT","TGGCTGGCT"]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140438401,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438401,"source":"dbSNP","seq_region_name":"7","id":"rs932502128","clinical_significance":[]},{"seq_region_name":"7","id":"rs1408351527","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140438407,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438407,"source":"dbSNP"},{"id":"rs1483176779","seq_region_name":"7","clinical_significance":[],"start":140438408,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140438408,"alleles":["G","A","T"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438412,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140438412,"seq_region_name":"7","id":"rs985299100","clinical_significance":[]},{"end":140438414,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140438414,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs543619658","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438417,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140438417,"clinical_significance":[],"seq_region_name":"7","id":"rs1799805206"},{"end":140438419,"alleles":["CCC","C"],"strand":1,"feature_type":"variation","start":140438417,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1308772798","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799805254","end":140438418,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140438418,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1294826581","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140438421,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438421},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799805292","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438423,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140438423},{"alleles":["T","C","G"],"end":140438424,"feature_type":"variation","strand":1,"source":"dbSNP","start":140438424,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1227169762"},{"end":140438425,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140438425,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs925873824","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438426,"source":"dbSNP","strand":1,"feature_type":"variation","end":140438426,"alleles":["T","G"],"seq_region_name":"7","id":"rs1316874097","clinical_significance":[]},{"start":140438427,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","G"],"end":140438427,"strand":1,"feature_type":"variation","id":"rs1156380759","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438429,"feature_type":"variation","strand":1,"end":140438429,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799805425"},{"clinical_significance":[],"id":"rs1401324605","seq_region_name":"7","feature_type":"variation","strand":1,"end":140438431,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438431},{"source":"dbSNP","start":140438435,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140438435,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799805465"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140438436,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438436,"clinical_significance":[],"id":"rs1799805488","seq_region_name":"7"},{"source":"dbSNP","start":140438440,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140438440,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1298708503","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1352810059","source":"dbSNP","start":140438441,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140438441,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1463509865","seq_region_name":"7","feature_type":"variation","strand":1,"end":140438443,"alleles":["GGG","GG"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438441},{"feature_type":"variation","strand":1,"end":140438444,"alleles":["T","A","C","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438444,"clinical_significance":[],"id":"rs1035769889","seq_region_name":"7"},{"id":"rs1799805668","seq_region_name":"7","clinical_significance":[],"end":140438447,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140438447,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs555793341","clinical_significance":[],"strand":1,"feature_type":"variation","end":140438451,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438451,"source":"dbSNP"},{"end":140438452,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140438452,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1182061638"},{"start":140438454,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140438454,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799805738","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799805756","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438455,"source":"dbSNP","strand":1,"feature_type":"variation","end":140438455,"alleles":["G","A"]},{"clinical_significance":[],"id":"rs1585446552","seq_region_name":"7","source":"dbSNP","start":140438456,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140438456,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799805788","feature_type":"variation","strand":1,"end":140438460,"alleles":["G","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438460},{"strand":1,"feature_type":"variation","end":140438462,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438462,"source":"dbSNP","id":"rs1423630178","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799805842","source":"dbSNP","start":140438463,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140438463,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1251813548","alleles":["G","T"],"end":140438464,"feature_type":"variation","strand":1,"source":"dbSNP","start":140438464,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"id":"rs574463478","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438465,"source":"dbSNP","strand":1,"feature_type":"variation","end":140438465,"alleles":["C","A","G","T"]},{"seq_region_name":"7","id":"rs543769130","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438466,"source":"dbSNP","strand":1,"feature_type":"variation","end":140438466,"alleles":["G","A","T"]},{"start":140438469,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["ACCATCC","ACCATCCACCATCC"],"end":140438475,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799805931","clinical_significance":[]},{"id":"rs1799805954","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140438473,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438473,"source":"dbSNP"},{"alleles":["C","G"],"end":140438475,"feature_type":"variation","strand":1,"source":"dbSNP","start":140438475,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1203890844"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438476,"feature_type":"variation","strand":1,"end":140438476,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs559921468"},{"seq_region_name":"7","id":"rs1799806000","clinical_significance":[],"strand":1,"feature_type":"variation","end":140438480,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438480,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1293493595","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140438485,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438485,"source":"dbSNP"},{"end":140438486,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140438486,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1242284083","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140438488,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438488,"clinical_significance":[],"seq_region_name":"7","id":"rs1799806055"},{"source":"dbSNP","start":140438489,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140438489,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799806076"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438494,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140438494,"seq_region_name":"7","id":"rs1435577489","clinical_significance":[]},{"alleles":["C","G","T"],"end":140438496,"strand":1,"feature_type":"variation","start":140438496,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1339675870","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs527580681","source":"dbSNP","start":140438497,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140438497,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1393065858","source":"dbSNP","start":140438499,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140438499,"alleles":["C","G"],"feature_type":"variation","strand":1},{"alleles":["C","G"],"end":140438501,"strand":1,"feature_type":"variation","start":140438501,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs2130199185","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140438505,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438505,"source":"dbSNP","seq_region_name":"7","id":"rs1348623474","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438512,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140438512,"seq_region_name":"7","id":"rs1307440472","clinical_significance":[]},{"seq_region_name":"7","id":"rs1411842613","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438513,"source":"dbSNP","strand":1,"feature_type":"variation","end":140438513,"alleles":["C","A","T"]},{"seq_region_name":"7","id":"rs1799806274","clinical_significance":[],"start":140438514,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["-","A"],"end":140438513,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140438514,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438514,"source":"dbSNP","seq_region_name":"7","id":"rs1405634516","clinical_significance":[]},{"alleles":["AAAAAAAAAAAA","AAAAAAAAAA","AAAAAAAAAAA","AAAAAAAAAAAAA","AAAAAAAAAAAAAA","AAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAA"],"end":140438526,"strand":1,"feature_type":"variation","start":140438515,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs553083726","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585446615","clinical_significance":[],"start":140438520,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140438520,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs184049984","end":140438521,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140438521,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs891770047","seq_region_name":"7","end":140438522,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140438522,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799806479","alleles":["A","T"],"end":140438526,"feature_type":"variation","strand":1,"source":"dbSNP","start":140438526,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs113852602","source":"dbSNP","start":140438527,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","A","C"],"end":140438527,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1490378518","source":"dbSNP","start":140438531,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140438531,"alleles":["C","T"],"feature_type":"variation","strand":1},{"end":140438532,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140438532,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs11520908"},{"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140438535,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438535,"clinical_significance":[],"seq_region_name":"7","id":"rs1799806624"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1292717910","feature_type":"variation","strand":1,"end":140438536,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438536},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438537,"feature_type":"variation","strand":1,"end":140438537,"alleles":["T","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1320441612"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438538,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140438538,"seq_region_name":"7","id":"rs2130199279","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799806701","clinical_significance":[],"strand":1,"feature_type":"variation","end":140438539,"alleles":["GG","GGG"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438538,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799806720","source":"dbSNP","start":140438539,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140438539,"alleles":["G","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1221348660","feature_type":"variation","strand":1,"end":140438540,"alleles":["T","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438540},{"seq_region_name":"7","id":"rs1799806764","clinical_significance":[],"strand":1,"feature_type":"variation","end":140438541,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438541,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1046274952","clinical_significance":[],"start":140438543,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140438543,"alleles":["C","A","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1799806813","clinical_significance":[],"start":140438544,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140438544,"alleles":["G","A","T"],"strand":1,"feature_type":"variation"},{"start":140438545,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","C"],"end":140438545,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799806833","clinical_significance":[]},{"alleles":["C","T"],"end":140438547,"strand":1,"feature_type":"variation","start":140438547,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1261085078","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140438548,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438548,"clinical_significance":[],"id":"rs1240937464","seq_region_name":"7"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438549,"feature_type":"variation","strand":1,"end":140438549,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs905932966"},{"source":"dbSNP","start":140438552,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140438552,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799806919"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1287683059","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438555,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140438555},{"clinical_significance":[],"seq_region_name":"7","id":"rs1179485797","end":140438557,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140438557,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438558,"feature_type":"variation","strand":1,"end":140438558,"alleles":["C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1250439899"},{"seq_region_name":"7","id":"rs1475281153","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140438566,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438566,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140438567,"alleles":["T","A","C","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438567,"source":"dbSNP","id":"rs7457619","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438568,"source":"dbSNP","strand":1,"feature_type":"variation","end":140438568,"alleles":["G","C","T"],"seq_region_name":"7","id":"rs1411583135","clinical_significance":[]},{"id":"rs1799807158","seq_region_name":"7","clinical_significance":[],"start":140438569,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140438569,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs895660783","end":140438571,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140438571,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"start":140438572,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140438572,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1563079957","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["GAGGCAGGAGAATGGCGTG","GAGGCAGGAGAATGGCGTGGAGGCAGGAGAATGGCGTG"],"end":140438594,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438576,"clinical_significance":[],"id":"rs2130199388","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1404670832","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438578,"feature_type":"variation","strand":1,"end":140438578,"alleles":["G","A"]},{"alleles":["G","C"],"end":140438582,"strand":1,"feature_type":"variation","start":140438582,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1799807255","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438585,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140438585,"seq_region_name":"7","id":"rs1455974785","clinical_significance":[]},{"source":"dbSNP","start":140438586,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140438586,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799807306"},{"source":"dbSNP","start":140438588,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140438588,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799807337","seq_region_name":"7"},{"end":140438594,"alleles":["TGGCGTG","TG"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140438588,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1170901636"},{"seq_region_name":"7","id":"rs1585446677","clinical_significance":[],"end":140438589,"alleles":["G","C","T"],"strand":1,"feature_type":"variation","start":140438589,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"start":140438591,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","A","T"],"end":140438591,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1356025186","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140438592,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438592,"clinical_significance":[],"seq_region_name":"7","id":"rs2885920"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438594,"feature_type":"variation","strand":1,"end":140438594,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799807514"},{"seq_region_name":"7","id":"rs1799807540","clinical_significance":[],"end":140438595,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140438595,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"alleles":["A","C","G"],"end":140438596,"strand":1,"feature_type":"variation","start":140438596,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs888030476","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140438600,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438600,"clinical_significance":[],"id":"rs1450630617","seq_region_name":"7"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438602,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140438602,"clinical_significance":[],"seq_region_name":"7","id":"rs1799807580"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799807601","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140438605,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438605},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140438606,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438606,"clinical_significance":[],"seq_region_name":"7","id":"rs1262004410"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1306350257","end":140438607,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140438607,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"alleles":["G","A"],"end":140438610,"feature_type":"variation","strand":1,"source":"dbSNP","start":140438610,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs904380412"},{"seq_region_name":"7","id":"rs1463396368","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438611,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140438611},{"seq_region_name":"7","id":"rs1267320898","clinical_significance":[],"end":140438612,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140438612,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"id":"rs1799807733","seq_region_name":"7","end":140438617,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140438617,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"id":"rs1799807756","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438618,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140438618},{"start":140438620,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140438620,"alleles":["A","-"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1224015171","clinical_significance":[]},{"seq_region_name":"7","id":"rs1325663898","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438621,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140438621},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799807838","source":"dbSNP","start":140438623,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140438623,"alleles":["C","A","G","T"],"feature_type":"variation","strand":1},{"end":140438624,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140438624,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1273138650","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438625,"feature_type":"variation","strand":1,"end":140438625,"alleles":["A","G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1350091424"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799807934","source":"dbSNP","start":140438629,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140438629,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1232641474","seq_region_name":"7","end":140438633,"alleles":["CGCGC","CGC"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140438629,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1000021429","clinical_significance":[],"start":140438630,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140438630,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438632,"feature_type":"variation","strand":1,"end":140438632,"alleles":["G","A"],"clinical_significance":[],"id":"rs1799807994","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799808013","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140438635,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438635,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438637,"source":"dbSNP","strand":1,"feature_type":"variation","end":140438637,"alleles":["T","C"],"id":"rs1415547292","seq_region_name":"7","clinical_significance":[]},{"end":140438640,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140438640,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs186279797","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140438641,"alleles":["C","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438641,"clinical_significance":[],"seq_region_name":"7","id":"rs1799808095"},{"clinical_significance":[],"id":"rs1799808115","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438643,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140438643},{"clinical_significance":[],"id":"rs1388331236","seq_region_name":"7","alleles":["C","T"],"end":140438644,"feature_type":"variation","strand":1,"source":"dbSNP","start":140438644,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1022898783","clinical_significance":[],"start":140438650,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","C","T"],"end":140438650,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs879820598","clinical_significance":[],"start":140438653,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["TGACTG","TG"],"end":140438658,"strand":1,"feature_type":"variation"},{"start":140438654,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","C"],"end":140438654,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799808216","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1471236856","source":"dbSNP","start":140438655,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140438655,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1228203808","seq_region_name":"7","end":140438660,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140438660,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1400712889","seq_region_name":"7","source":"dbSNP","start":140438668,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140438668,"alleles":["C","G","T"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140438669,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438669,"source":"dbSNP","seq_region_name":"7","id":"rs529404212","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438670,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140438670,"clinical_significance":[],"id":"rs1009574627","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1190088377","clinical_significance":[],"strand":1,"feature_type":"variation","end":140438675,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438675,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1373240238","clinical_significance":[],"strand":1,"feature_type":"variation","end":140438681,"alleles":["AAAAAAA","AAAAAAAA"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438675,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799808599","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438678,"source":"dbSNP","strand":1,"feature_type":"variation","end":140438678,"alleles":["A","G"]},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140438682,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438682,"source":"dbSNP","seq_region_name":"7","id":"rs111851305","clinical_significance":[]},{"id":"rs1585446769","seq_region_name":"7","clinical_significance":[],"start":140438682,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","TT"],"end":140438682,"strand":1,"feature_type":"variation"},{"start":140438683,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140438683,"alleles":["A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs78257701","clinical_significance":[]},{"start":140438683,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140438690,"alleles":["AAAAAAAA","AAAAAAA","AAAAAAAAA"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs78096181","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140438688,"alleles":["A","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438688,"clinical_significance":[],"seq_region_name":"7","id":"rs1204125212"},{"start":140438693,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140438693,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs76428299","clinical_significance":[]},{"start":140438697,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140438697,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs76784993","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799808856","clinical_significance":[],"strand":1,"feature_type":"variation","end":140438704,"alleles":["TAAAATAA","TAA"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438697,"source":"dbSNP"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438699,"feature_type":"variation","strand":1,"end":140438699,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1029856635"},{"clinical_significance":[],"id":"rs953794021","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140438700,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438700},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438704,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140438704,"clinical_significance":[],"seq_region_name":"7","id":"rs1226415606"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1364810562","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438709,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140438709},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438711,"source":"dbSNP","strand":1,"feature_type":"variation","end":140438711,"alleles":["T","C","G"],"id":"rs1189073113","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs963596569","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438713,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140438713},{"clinical_significance":[],"seq_region_name":"7","id":"rs1235188412","source":"dbSNP","start":140438714,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140438714,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1454922657","clinical_significance":[],"end":140438715,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140438715,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"feature_type":"variation","strand":1,"end":140438726,"alleles":["AGCTAAG","AG"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438720,"clinical_significance":[],"seq_region_name":"7","id":"rs1799809067"},{"strand":1,"feature_type":"variation","end":140438731,"alleles":["TAAGAGTAA","TAA"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438723,"source":"dbSNP","id":"rs1799809089","seq_region_name":"7","clinical_significance":[]},{"start":140438729,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140438729,"alleles":["T","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799809109","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799809124","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438731,"source":"dbSNP","strand":1,"feature_type":"variation","end":140438731,"alleles":["A","C","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799809153","alleles":["A","C"],"end":140438737,"feature_type":"variation","strand":1,"source":"dbSNP","start":140438737,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799809183","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438742,"feature_type":"variation","strand":1,"alleles":["ACTCAC","AC"],"end":140438747},{"alleles":["C","T"],"end":140438745,"strand":1,"feature_type":"variation","start":140438745,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1799809208","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1339186288","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438746,"feature_type":"variation","strand":1,"end":140438746,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs565989345","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140438748,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438748},{"alleles":["AAA","AA"],"end":140438758,"strand":1,"feature_type":"variation","start":140438756,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1799809285","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438761,"feature_type":"variation","strand":1,"end":140438761,"alleles":["G","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799809302"},{"start":140438765,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140438765,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs985716556","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1411068623","clinical_significance":[],"strand":1,"feature_type":"variation","end":140438766,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438766,"source":"dbSNP"},{"alleles":["G","A"],"end":140438767,"strand":1,"feature_type":"variation","start":140438767,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs970711461","clinical_significance":[]},{"end":140438772,"alleles":["GTTGTT","GTT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140438767,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1186972400"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438773,"source":"dbSNP","strand":1,"feature_type":"variation","end":140438773,"alleles":["A","C"],"seq_region_name":"7","id":"rs1002739406","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799809426","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140438776,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438776,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438779,"source":"dbSNP","strand":1,"feature_type":"variation","end":140438779,"alleles":["C","T"],"seq_region_name":"7","id":"rs1033750657","clinical_significance":[]},{"clinical_significance":[],"id":"rs1170016471","seq_region_name":"7","end":140438782,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140438782,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"start":140438784,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140438784,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1421411514","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438785,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140438785,"seq_region_name":"7","id":"rs1799809526","clinical_significance":[]},{"seq_region_name":"7","id":"rs935914191","clinical_significance":[],"start":140438795,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140438795,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs963908704","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438800,"feature_type":"variation","strand":1,"end":140438800,"alleles":["T","C"]},{"clinical_significance":[],"id":"rs1799809586","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438802,"feature_type":"variation","strand":1,"end":140438802,"alleles":["T","C"]},{"start":140438803,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140438803,"alleles":["A","G"],"strand":1,"feature_type":"variation","id":"rs1799809603","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1585446840","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438803,"feature_type":"variation","strand":1,"end":140438812,"alleles":["ATACAATACA","ATACA"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs973567638","alleles":["T","C"],"end":140438804,"feature_type":"variation","strand":1,"source":"dbSNP","start":140438804,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1585446841","seq_region_name":"7","source":"dbSNP","start":140438812,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140438812,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs913152212","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140438814,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438814},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438815,"feature_type":"variation","strand":1,"end":140438815,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799809717"},{"seq_region_name":"7","id":"rs950119650","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438816,"source":"dbSNP","strand":1,"feature_type":"variation","end":140438816,"alleles":["T","C"]},{"strand":1,"feature_type":"variation","end":140438820,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438820,"source":"dbSNP","seq_region_name":"7","id":"rs1186724231","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140438823,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438823,"source":"dbSNP","seq_region_name":"7","id":"rs539736323","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1336271853","source":"dbSNP","start":140438828,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140438828,"alleles":["G","-"],"feature_type":"variation","strand":1},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438828,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140438828,"clinical_significance":[],"seq_region_name":"7","id":"rs1585446851"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799809872","feature_type":"variation","strand":1,"end":140438829,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438829},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799809896","source":"dbSNP","start":140438831,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["TATAATTAT","TAT"],"end":140438839,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1275197723","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438833,"feature_type":"variation","strand":1,"end":140438833,"alleles":["T","A"]},{"seq_region_name":"7","id":"rs1203130569","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438838,"source":"dbSNP","strand":1,"feature_type":"variation","end":140438838,"alleles":["A","G"]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438838,"source":"dbSNP","strand":1,"feature_type":"variation","end":140438842,"alleles":["ATGAT","AT"],"id":"rs1357460702","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","C"],"end":140438839,"feature_type":"variation","strand":1,"source":"dbSNP","start":140438839,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799809973"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1027000688","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438840,"feature_type":"variation","strand":1,"end":140438840,"alleles":["G","T"]},{"alleles":["AAAAA","AA","AAAA"],"end":140438856,"strand":1,"feature_type":"variation","start":140438852,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1447962512","clinical_significance":[]},{"alleles":["AATAATA","AATA"],"end":140438861,"feature_type":"variation","strand":1,"source":"dbSNP","start":140438855,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1292820154","seq_region_name":"7"},{"seq_region_name":"7","id":"rs2130199830","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438860,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TATTA","TA"],"end":140438864},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438862,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140438862,"seq_region_name":"7","id":"rs1799810048","clinical_significance":[]},{"seq_region_name":"7","id":"rs1248566273","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140438871,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438871,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799810093","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438872,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140438872},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799810109","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438875,"feature_type":"variation","strand":1,"end":140438875,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1354665509","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140438876,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438876},{"clinical_significance":[],"seq_region_name":"7","id":"rs1284018766","feature_type":"variation","strand":1,"end":140438878,"alleles":["G","A","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438878},{"seq_region_name":"7","id":"rs1799810171","clinical_significance":[],"end":140438883,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140438883,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"id":"rs1443561291","seq_region_name":"7","source":"dbSNP","start":140438889,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140438889,"feature_type":"variation","strand":1},{"alleles":["G","A","T"],"end":140438890,"strand":1,"feature_type":"variation","start":140438890,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs950928206","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438892,"feature_type":"variation","strand":1,"end":140438892,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs557989095"},{"seq_region_name":"7","id":"rs1309253080","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438897,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140438897},{"clinical_significance":[],"seq_region_name":"7","id":"rs905958830","source":"dbSNP","start":140438898,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","C","G"],"end":140438898,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140438899,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438899,"source":"dbSNP","seq_region_name":"7","id":"rs987102466","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799810317","clinical_significance":[],"start":140438900,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["CTTAC","C"],"end":140438904,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1799810342","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140438901,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438901,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1369508903","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438905,"feature_type":"variation","strand":1,"end":140438905,"alleles":["A","-"]},{"seq_region_name":"7","id":"rs1799810386","clinical_significance":[],"strand":1,"feature_type":"variation","end":140438906,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438906,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1367969717","source":"dbSNP","start":140438908,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140438908,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1163853614","end":140438911,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140438911,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140438912,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438912,"clinical_significance":[],"seq_region_name":"7","id":"rs1799810448"},{"end":140438918,"alleles":["GTCGTC","GTC"],"strand":1,"feature_type":"variation","start":140438913,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1226696266","clinical_significance":[]},{"start":140438915,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140438915,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs570018488","clinical_significance":[]},{"seq_region_name":"7","id":"rs1049226728","clinical_significance":[],"start":140438916,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A","C"],"end":140438916,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140438917,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438917,"source":"dbSNP","seq_region_name":"7","id":"rs1470439737","clinical_significance":[]},{"alleles":["C","G","T"],"end":140438918,"strand":1,"feature_type":"variation","start":140438918,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1253894960","clinical_significance":[]},{"end":140438919,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140438919,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs537221021","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs911591341","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438924,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140438924},{"alleles":["G","A"],"end":140438927,"strand":1,"feature_type":"variation","start":140438927,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs887979958","clinical_significance":[]},{"id":"rs943033991","seq_region_name":"7","clinical_significance":[],"end":140438931,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140438931,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"id":"rs1799810690","seq_region_name":"7","clinical_significance":[],"start":140438932,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140438932,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"start":140438936,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140438936,"alleles":["C","A"],"strand":1,"feature_type":"variation","id":"rs1269758908","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799810736","clinical_significance":[],"start":140438938,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","G"],"end":140438938,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140438941,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438941,"source":"dbSNP","seq_region_name":"7","id":"rs1799810756","clinical_significance":[]},{"clinical_significance":[],"id":"rs974929204","seq_region_name":"7","source":"dbSNP","start":140438945,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","C","G"],"end":140438945,"feature_type":"variation","strand":1},{"alleles":["A","G"],"end":140438947,"strand":1,"feature_type":"variation","start":140438947,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs2130199950","clinical_significance":[]},{"id":"rs774344477","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140438949,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140438949},{"seq_region_name":"7","id":"rs1015152997","clinical_significance":[],"end":140438950,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140438950,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs902081478","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438957,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140438957},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799810872","alleles":["T","C"],"end":140438966,"feature_type":"variation","strand":1,"source":"dbSNP","start":140438966,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1799810888","seq_region_name":"7","source":"dbSNP","start":140438966,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","TT"],"end":140438966,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1289602613","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438969,"feature_type":"variation","strand":1,"end":140438984,"alleles":["AGGAATTGTCTTTTAG","AG"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs935854446","feature_type":"variation","strand":1,"end":140438971,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438971},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130199987","alleles":["A","C"],"end":140438972,"feature_type":"variation","strand":1,"source":"dbSNP","start":140438972,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438982,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140438982,"clinical_significance":[],"seq_region_name":"7","id":"rs2130199988"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799810971","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140438983,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438983},{"clinical_significance":[],"id":"rs1799810995","seq_region_name":"7","alleles":["A","G"],"end":140438985,"feature_type":"variation","strand":1,"source":"dbSNP","start":140438985,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs998273765","clinical_significance":[],"alleles":["G","A"],"end":140438991,"strand":1,"feature_type":"variation","start":140438991,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"feature_type":"variation","strand":1,"end":140438997,"alleles":["G","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140438997,"clinical_significance":[],"seq_region_name":"7","id":"rs2130200003"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439001,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140439001,"seq_region_name":"7","id":"rs2130200008","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130200016","clinical_significance":[],"strand":1,"feature_type":"variation","end":140439004,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439004,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140439005,"alleles":["A","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439005,"clinical_significance":[],"seq_region_name":"7","id":"rs1799811020"},{"seq_region_name":"7","id":"rs527491853","clinical_significance":[],"start":140439007,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","T"],"end":140439007,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs535317004","clinical_significance":[],"end":140439008,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140439008,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140439010,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439010,"source":"dbSNP","seq_region_name":"7","id":"rs1799811091","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130200042","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439012,"feature_type":"variation","strand":1,"end":140439012,"alleles":["A","T"]},{"id":"rs1799811111","seq_region_name":"7","clinical_significance":[],"start":140439013,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140439019,"alleles":["TTTCTTT","TTT"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439013,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TTTCTTTTT","TTT"],"end":140439021,"id":"rs1349313217","seq_region_name":"7","clinical_significance":[]},{"start":140439013,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140439039,"alleles":["TTTCTTTTTTTTTCTTTCTTTTTTTTT","TTTCTTTTTTTTT"],"strand":1,"feature_type":"variation","id":"rs1799811160","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799811175","clinical_significance":[],"start":140439015,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["TCT","T"],"end":140439017,"strand":1,"feature_type":"variation"},{"alleles":["C","T"],"end":140439016,"strand":1,"feature_type":"variation","start":140439016,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1438162451","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799811217","alleles":["C","-"],"end":140439016,"feature_type":"variation","strand":1,"source":"dbSNP","start":140439016,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"end":140439017,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140439017,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs953931975","clinical_significance":[]},{"alleles":["TTTTTTTTT","TTTTT","TTTTTT","TTTTTTTT","TTTTTTTTTT"],"end":140439025,"feature_type":"variation","strand":1,"source":"dbSNP","start":140439017,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1303273503"},{"seq_region_name":"7","id":"rs1799811313","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["TTTTTTTTTCTTT","TTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTCTTT"],"end":140439029,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439017,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs985176391","source":"dbSNP","start":140439019,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["TTTTTTTCTTT","TTT"],"end":140439029,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1215871684","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439020,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140439020},{"strand":1,"feature_type":"variation","alleles":["-","A"],"end":140439020,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439021,"source":"dbSNP","id":"rs2130200091","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585446953","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439021,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140439021},{"strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140439022,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439022,"source":"dbSNP","id":"rs891725953","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439023,"source":"dbSNP","strand":1,"feature_type":"variation","end":140439023,"alleles":["T","A","C","G"],"seq_region_name":"7","id":"rs949982679","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs140001005","source":"dbSNP","start":140439023,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140439033,"alleles":["TTTCTTTCTTT","TTTCTTT"],"feature_type":"variation","strand":1},{"start":140439024,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140439028,"alleles":["TTCTT","TT"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1246347180","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799811538","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["TTCTTTCTT","TT"],"end":140439032,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439024,"source":"dbSNP"},{"source":"dbSNP","start":140439025,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140439025,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1045676316"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439025,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TCT","T"],"end":140439027,"seq_region_name":"7","id":"rs1799811585","clinical_significance":[]},{"seq_region_name":"7","id":"rs374608477","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439026,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140439026},{"source":"dbSNP","start":140439026,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140439026,"alleles":["C","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1249896685"},{"seq_region_name":"7","id":"rs1799811629","clinical_significance":[],"start":140439026,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140439026,"alleles":["C","CC"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1799811670","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["CTTTC","-"],"end":140439030,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439026},{"seq_region_name":"7","id":"rs1431076061","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140439027,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439027,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["TTT","T","TT","TTTT","TTTTT","TTTTTT","TTTTTTTT","TTTTTTTTT","TTTTTTTTTT","TTTTTTTTTTT","TTTTTTTTTTTTT","TTTTTTTTTTTTTT","TTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTT"],"end":140439029,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439027,"clinical_significance":[],"seq_region_name":"7","id":"rs1324968321"},{"seq_region_name":"7","id":"rs1219237855","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["TTTCTTTT","TTT"],"end":140439034,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439027,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1220459726","clinical_significance":[],"strand":1,"feature_type":"variation","end":140439035,"alleles":["TTTCTTTTT","TTT"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439027,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1365004770","clinical_significance":[],"start":140439027,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140439036,"alleles":["TTTCTTTTTT","TTT"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799811880","alleles":["TTTCTTTTTTT","TTT"],"end":140439037,"feature_type":"variation","strand":1,"source":"dbSNP","start":140439027,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"id":"rs1799811893","seq_region_name":"7","clinical_significance":[],"start":140439027,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140439040,"alleles":["TTTCTTTTTTTTTT","TTT"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439027,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TTTCTTTTTTTTTTTTT","TTT"],"end":140439043,"id":"rs1032756802","seq_region_name":"7","clinical_significance":[]},{"end":140439028,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140439028,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs906555750","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs769703192","feature_type":"variation","strand":1,"alleles":["TTCTT","TT"],"end":140439032,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439028},{"feature_type":"variation","strand":1,"end":140439031,"alleles":["TCT","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439029,"clinical_significance":[],"seq_region_name":"7","id":"rs201604586"},{"strand":1,"feature_type":"variation","end":140439030,"alleles":["C","A","G","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439030,"source":"dbSNP","seq_region_name":"7","id":"rs11520911","clinical_significance":[]},{"id":"rs56685347","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","-"],"end":140439030,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439030,"source":"dbSNP"},{"id":"rs1246569032","seq_region_name":"7","clinical_significance":[],"alleles":["T","A","C"],"end":140439031,"strand":1,"feature_type":"variation","start":140439031,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"feature_type":"variation","strand":1,"alleles":["TTTTTTTTTTTTTTTTT","TTTTTTTTTT","TTTTTTTTTTT","TTTTTTTTTTTTT","TTTTTTTTTTTTTT","TTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT"],"end":140439047,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439031,"clinical_significance":[],"seq_region_name":"7","id":"rs71170998"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1478497472","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439032,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140439032},{"start":140439033,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140439033,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs957232183","clinical_significance":[]},{"seq_region_name":"7","id":"rs1423311147","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439034,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140439034},{"end":140439035,"alleles":["T","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140439035,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1414043399"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439036,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140439036,"id":"rs988626268","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439037,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140439037,"clinical_significance":[],"id":"rs1585447077","seq_region_name":"7"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439039,"feature_type":"variation","strand":1,"end":140439038,"alleles":["-","AC"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130200275"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1277355995","source":"dbSNP","start":140439040,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140439040,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130200282","feature_type":"variation","strand":1,"end":140439041,"alleles":["T","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439041},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563080125","end":140439044,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140439044,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799812497","end":140439046,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140439046,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"end":140439048,"alleles":["TTG","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140439046,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1433463575"},{"start":140439046,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["TTGA","-"],"end":140439049,"strand":1,"feature_type":"variation","id":"rs1799812544","seq_region_name":"7","clinical_significance":[]},{"start":140439047,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140439048,"alleles":["TG","-"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1228681339","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439048,"feature_type":"variation","strand":1,"alleles":["G","-"],"end":140439048,"clinical_significance":[],"id":"rs1320338519","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439048,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140439048,"id":"rs1372093965","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1234983370","seq_region_name":"7","source":"dbSNP","start":140439050,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140439050,"alleles":["G","A","T"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439054,"source":"dbSNP","strand":1,"feature_type":"variation","end":140439054,"alleles":["G","C"],"id":"rs1272780450","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799812682","seq_region_name":"7","source":"dbSNP","start":140439056,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140439056,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1799812701","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140439057,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439057,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1585447100","clinical_significance":[],"start":140439061,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140439061,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140439062,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439062,"source":"dbSNP","seq_region_name":"7","id":"rs1434092959","clinical_significance":[]},{"source":"dbSNP","start":140439064,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","A","G"],"end":140439064,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs574450496","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799812769","clinical_significance":[],"start":140439065,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140439065,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140439066,"alleles":["G","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439066,"clinical_significance":[],"seq_region_name":"7","id":"rs1585447107"},{"start":140439067,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140439067,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799812822","clinical_significance":[]},{"seq_region_name":"7","id":"rs71520095","clinical_significance":[],"start":140439067,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["TT","TTT"],"end":140439068,"strand":1,"feature_type":"variation"},{"id":"rs1799812869","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439068,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140439068},{"end":140439069,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140439069,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585447111"},{"id":"rs913152514","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140439075,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439075,"source":"dbSNP"},{"alleles":["T","A"],"end":140439077,"strand":1,"feature_type":"variation","start":140439077,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1464523154","seq_region_name":"7","clinical_significance":[]},{"end":140439081,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140439081,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799812961","seq_region_name":"7"},{"id":"rs1585447125","seq_region_name":"7","clinical_significance":[],"start":140439082,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140439082,"alleles":["T","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs971313772","feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140439086,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439086},{"feature_type":"variation","strand":1,"end":140439087,"alleles":["T","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439087,"clinical_significance":[],"id":"rs1585447133","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130200383","feature_type":"variation","strand":1,"end":140439091,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439091},{"start":140439092,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140439092,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799813052","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585447136","clinical_significance":[],"start":140439093,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140439093,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1171307022","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439105,"feature_type":"variation","strand":1,"end":140439106,"alleles":["TT","T"]},{"id":"rs1799813124","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140439108,"strand":1,"feature_type":"variation","start":140439108,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"id":"rs1799813147","seq_region_name":"7","feature_type":"variation","strand":1,"end":140439110,"alleles":["G","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439110},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439111,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140439111,"seq_region_name":"7","id":"rs1585447139","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799813193","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439114,"feature_type":"variation","strand":1,"end":140439114,"alleles":["C","A"]},{"clinical_significance":[],"id":"rs1463508731","seq_region_name":"7","feature_type":"variation","strand":1,"end":140439115,"alleles":["A","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439115},{"start":140439119,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140439119,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130200429","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799813242","seq_region_name":"7","source":"dbSNP","start":140439121,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140439121,"alleles":["C","T"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140439123,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439123,"source":"dbSNP","id":"rs1002195413","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439125,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140439125,"id":"rs1799813288","seq_region_name":"7","clinical_significance":[]},{"id":"rs1431844938","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140439126,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439126,"source":"dbSNP"},{"seq_region_name":"7","id":"rs2130200452","clinical_significance":[],"start":140439130,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140439130,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140439136,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439136,"clinical_significance":[],"seq_region_name":"7","id":"rs1034192937"},{"id":"rs1799813467","seq_region_name":"7","clinical_significance":[],"start":140439141,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140439141,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140439146,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439146,"clinical_significance":[],"seq_region_name":"7","id":"rs1188284247"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1445642883","end":140439148,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140439148,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140439152,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140439152,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1253400647"},{"seq_region_name":"7","id":"rs1799813563","clinical_significance":[],"alleles":["C","T"],"end":140439154,"strand":1,"feature_type":"variation","start":140439154,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140439155,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439155,"clinical_significance":[],"seq_region_name":"7","id":"rs2130200475"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799813580","end":140439156,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140439156,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1453170674","end":140439157,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140439157,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140439160,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140439160,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1585447155","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["GCTCGGACCACGGGCTGCTC","GCTC"],"end":140439179,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439160,"source":"dbSNP","seq_region_name":"7","id":"rs1180593330","clinical_significance":[]},{"id":"rs1799813664","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140439161,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439161,"source":"dbSNP"},{"id":"rs899223793","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439163,"source":"dbSNP","strand":1,"feature_type":"variation","end":140439163,"alleles":["C","G","T"]},{"start":140439164,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A","C"],"end":140439164,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs535243612","clinical_significance":[]},{"id":"rs1799813834","seq_region_name":"7","clinical_significance":[],"end":140439169,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140439169,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799813855","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140439170,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439170},{"start":140439171,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A","C"],"end":140439171,"strand":1,"feature_type":"variation","id":"rs1477808978","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439173,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140439173,"seq_region_name":"7","id":"rs771865728","clinical_significance":[]},{"alleles":["C","T"],"end":140439179,"feature_type":"variation","strand":1,"source":"dbSNP","start":140439179,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs2130200520","seq_region_name":"7"},{"seq_region_name":"7","id":"rs190353315","clinical_significance":[],"strand":1,"feature_type":"variation","end":140439182,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439182,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439192,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140439192,"seq_region_name":"7","id":"rs1456113421","clinical_significance":[]},{"id":"rs1394212946","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140439196,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439196,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799814248","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439201,"source":"dbSNP","strand":1,"feature_type":"variation","end":140439201,"alleles":["A","C"]},{"id":"rs1799814266","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439220,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140439220},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140439223,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439223,"clinical_significance":[],"id":"rs1799814292","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799814392","alleles":["A","C"],"end":140439224,"feature_type":"variation","strand":1,"source":"dbSNP","start":140439224,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1799814411","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439225,"source":"dbSNP","strand":1,"feature_type":"variation","end":140439225,"alleles":["G","A","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799814431","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140439228,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439228},{"clinical_significance":[],"seq_region_name":"7","id":"rs1378421484","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439231,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140439231},{"start":140439231,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140439234,"alleles":["GGAT","GGATGGAT"],"strand":1,"feature_type":"variation","id":"rs1799814468","seq_region_name":"7","clinical_significance":[]},{"end":140439232,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140439232,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799814494","clinical_significance":[]},{"end":140439233,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140439233,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs987720049","clinical_significance":[]},{"source":"dbSNP","start":140439234,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140439234,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799814540","seq_region_name":"7"},{"id":"rs909282153","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140439237,"strand":1,"feature_type":"variation","start":140439237,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1368896964","clinical_significance":[],"strand":1,"feature_type":"variation","end":140439239,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439239,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs571903545","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140439241,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439241},{"start":140439242,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140439242,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs760135831","clinical_significance":[]},{"id":"rs1370563106","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140439243,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439243,"source":"dbSNP"},{"id":"rs1388959047","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140439244,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439244,"source":"dbSNP"},{"id":"rs1799814704","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439246,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140439246},{"clinical_significance":[],"seq_region_name":"7","id":"rs1321956689","feature_type":"variation","strand":1,"alleles":["GCCACTGGGCCGGCCA","GCCA"],"end":140439261,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439246},{"seq_region_name":"7","id":"rs1799814763","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439247,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140439247},{"clinical_significance":[],"seq_region_name":"7","id":"rs1163195011","source":"dbSNP","start":140439248,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140439248,"alleles":["C","G"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140439253,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439253,"source":"dbSNP","id":"rs1799814808","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439256,"feature_type":"variation","strand":1,"end":140439256,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1330203293"},{"clinical_significance":[],"seq_region_name":"7","id":"rs964747842","feature_type":"variation","strand":1,"end":140439257,"alleles":["G","A","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439257},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439259,"source":"dbSNP","strand":1,"feature_type":"variation","end":140439259,"alleles":["C","A"],"seq_region_name":"7","id":"rs2130200622","clinical_significance":[]},{"alleles":["C","T"],"end":140439260,"strand":1,"feature_type":"variation","start":140439260,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799814868","clinical_significance":[]},{"alleles":["G","T"],"end":140439263,"strand":1,"feature_type":"variation","start":140439263,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799814887","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585447235","feature_type":"variation","strand":1,"end":140439267,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439267},{"clinical_significance":[],"seq_region_name":"7","id":"rs1182217876","feature_type":"variation","strand":1,"end":140439274,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439274},{"clinical_significance":[],"id":"rs2130200638","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140439275,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439275},{"seq_region_name":"7","id":"rs1483761809","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439276,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140439276},{"id":"rs1249043003","seq_region_name":"7","clinical_significance":[],"end":140439280,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140439280,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs974413661","clinical_significance":[],"start":140439282,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140439282,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"id":"rs1203954977","seq_region_name":"7","clinical_significance":[],"start":140439283,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140439283,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1488641328","clinical_significance":[],"end":140439286,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140439286,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"alleles":["C","A"],"end":140439289,"strand":1,"feature_type":"variation","start":140439289,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799815051","clinical_significance":[]},{"alleles":["A","G"],"end":140439293,"feature_type":"variation","strand":1,"source":"dbSNP","start":140439293,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1442424259"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439294,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140439294,"seq_region_name":"7","id":"rs1799815139","clinical_significance":[]},{"alleles":["T","C"],"end":140439296,"feature_type":"variation","strand":1,"source":"dbSNP","start":140439296,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799815166"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439298,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140439298,"clinical_significance":[],"seq_region_name":"7","id":"rs1036461305"},{"source":"dbSNP","start":140439299,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140439299,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs925699425"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439300,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GG","G"],"end":140439301,"seq_region_name":"7","id":"rs1242357967","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140439301,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439301,"source":"dbSNP","seq_region_name":"7","id":"rs1320971503","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439305,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140439305,"id":"rs935729918","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140439310,"alleles":["T","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439310,"clinical_significance":[],"seq_region_name":"7","id":"rs1799815294"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130200718","source":"dbSNP","start":140439314,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140439314,"alleles":["G","A"],"feature_type":"variation","strand":1},{"start":140439315,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140439315,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs11978135","clinical_significance":[]},{"start":140439317,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","T"],"end":140439317,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799815438","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439319,"feature_type":"variation","strand":1,"alleles":["TTGTT","TT"],"end":140439323,"clinical_significance":[],"seq_region_name":"7","id":"rs1585447273"},{"seq_region_name":"7","id":"rs766477894","clinical_significance":[],"end":140439321,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140439321,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439322,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140439322,"clinical_significance":[],"seq_region_name":"7","id":"rs2130200753"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1326375410","source":"dbSNP","start":140439323,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140439323,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs145776049","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439325,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140439325},{"source":"dbSNP","start":140439330,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140439330,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585447285"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1051209886","source":"dbSNP","start":140439333,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140439333,"alleles":["A","G"],"feature_type":"variation","strand":1},{"id":"rs1799815628","seq_region_name":"7","clinical_significance":[],"start":140439336,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140439336,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140439337,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439337,"clinical_significance":[],"seq_region_name":"7","id":"rs949848013"},{"seq_region_name":"7","id":"rs1393168196","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140439339,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439339,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799815764","feature_type":"variation","strand":1,"end":140439341,"alleles":["T","C","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439341},{"strand":1,"feature_type":"variation","end":140439344,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439344,"source":"dbSNP","seq_region_name":"7","id":"rs1045706508","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs576417752","alleles":["C","A","G"],"end":140439350,"feature_type":"variation","strand":1,"source":"dbSNP","start":140439350,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439351,"source":"dbSNP","strand":1,"feature_type":"variation","end":140439351,"alleles":["C","G"],"id":"rs543629202","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140439353,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439353,"source":"dbSNP","seq_region_name":"7","id":"rs1799815857","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799815876","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439355,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140439355},{"alleles":["G","A"],"end":140439359,"feature_type":"variation","strand":1,"source":"dbSNP","start":140439359,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1358339083"},{"id":"rs889496587","seq_region_name":"7","clinical_significance":[],"alleles":["GGGG","GGGGG"],"end":140439362,"strand":1,"feature_type":"variation","start":140439359,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"start":140439360,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140439360,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs905748698","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585447310","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439363,"feature_type":"variation","strand":1,"end":140439363,"alleles":["T","G"]},{"seq_region_name":"7","id":"rs1207892891","clinical_significance":[],"alleles":["C","T"],"end":140439368,"strand":1,"feature_type":"variation","start":140439368,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"start":140439373,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140439373,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs148976268","clinical_significance":[]},{"source":"dbSNP","start":140439374,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140439374,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1346253683","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799816047","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439377,"feature_type":"variation","strand":1,"alleles":["TGCTGCTG","TGCTG"],"end":140439384},{"start":140439381,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","C"],"end":140439381,"strand":1,"feature_type":"variation","id":"rs1032787932","seq_region_name":"7","clinical_significance":[]},{"end":140439382,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140439382,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1471917191"},{"seq_region_name":"7","id":"rs1409119127","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439384,"source":"dbSNP","strand":1,"feature_type":"variation","end":140439384,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1180899080","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439385,"source":"dbSNP","strand":1,"feature_type":"variation","end":140439385,"alleles":["T","C"]},{"consequence_type":"TF_binding_site_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439389,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140439389,"clinical_significance":[],"seq_region_name":"7","id":"rs2130200865"},{"consequence_type":"TF_binding_site_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439391,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140439391,"clinical_significance":[],"seq_region_name":"7","id":"rs1799816125"},{"clinical_significance":[],"id":"rs1451280709","seq_region_name":"7","consequence_type":"TF_binding_site_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439392,"feature_type":"variation","strand":1,"end":140439392,"alleles":["C","T"]},{"start":140439394,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"TF_binding_site_variant","alleles":["T","C"],"end":140439394,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1433351960","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799816181","feature_type":"variation","strand":1,"alleles":["T","A"],"end":140439403,"consequence_type":"TF_binding_site_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439403},{"clinical_significance":[],"seq_region_name":"7","id":"rs759509506","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439410,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140439410},{"seq_region_name":"7","id":"rs1799816227","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439412,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140439412},{"strand":1,"feature_type":"variation","end":140439413,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439413,"source":"dbSNP","seq_region_name":"7","id":"rs1254081842","clinical_significance":[]},{"seq_region_name":"7","id":"rs1010090858","clinical_significance":[],"alleles":["T","C"],"end":140439417,"strand":1,"feature_type":"variation","start":140439417,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"feature_type":"variation","strand":1,"end":140439418,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439418,"clinical_significance":[],"seq_region_name":"7","id":"rs2130200904"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439420,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140439420,"clinical_significance":[],"seq_region_name":"7","id":"rs1020075164"},{"strand":1,"feature_type":"variation","alleles":["G","C","T"],"end":140439421,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439421,"source":"dbSNP","id":"rs1471687073","seq_region_name":"7","clinical_significance":[]},{"id":"rs1327067383","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439422,"source":"dbSNP","strand":1,"feature_type":"variation","end":140439422,"alleles":["G","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1287745998","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140439423,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439423},{"clinical_significance":[],"id":"rs1181550929","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439425,"feature_type":"variation","strand":1,"end":140439425,"alleles":["T","C"]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140439426,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439426,"source":"dbSNP","seq_region_name":"7","id":"rs1799816394","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439428,"feature_type":"variation","strand":1,"end":140439428,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799816410"},{"alleles":["C","T"],"end":140439432,"feature_type":"variation","strand":1,"source":"dbSNP","start":140439432,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1369592556"},{"alleles":["G","T"],"end":140439435,"feature_type":"variation","strand":1,"source":"dbSNP","start":140439435,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799816450"},{"seq_region_name":"7","id":"rs1459880875","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439438,"source":"dbSNP","strand":1,"feature_type":"variation","end":140439438,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1799816487","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439438,"source":"dbSNP","strand":1,"feature_type":"variation","end":140439439,"alleles":["GG","G"]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439439,"source":"dbSNP","strand":1,"feature_type":"variation","end":140439439,"alleles":["G","A","C"],"seq_region_name":"7","id":"rs765585629","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799816535","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439443,"feature_type":"variation","strand":1,"end":140439443,"alleles":["T","C"]},{"alleles":["G","A"],"end":140439447,"feature_type":"variation","strand":1,"source":"dbSNP","start":140439447,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs575062701"},{"strand":1,"feature_type":"variation","alleles":["T","A","G"],"end":140439456,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439456,"source":"dbSNP","seq_region_name":"7","id":"rs1799816583","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439456,"feature_type":"variation","strand":1,"alleles":["TCTCTCT","TCT"],"end":140439462,"clinical_significance":[],"id":"rs1390417651","seq_region_name":"7"},{"start":140439461,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140439461,"strand":1,"feature_type":"variation","id":"rs1386468516","seq_region_name":"7","clinical_significance":[]},{"start":140439467,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140439467,"strand":1,"feature_type":"variation","id":"rs1799816658","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585447368","source":"dbSNP","start":140439470,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140439470,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140439474,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439474,"clinical_significance":[],"seq_region_name":"7","id":"rs1799816691"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1389795913","end":140439480,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140439480,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439491,"feature_type":"variation","strand":1,"end":140439491,"alleles":["T","C"],"clinical_significance":[],"id":"rs1799816734","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439494,"source":"dbSNP","strand":1,"feature_type":"variation","end":140439494,"alleles":["G","A"],"seq_region_name":"7","id":"rs1458740214","clinical_significance":[]},{"seq_region_name":"7","id":"rs981416028","clinical_significance":[],"start":140439502,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140439502,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799816805","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140439503,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439503},{"clinical_significance":[],"seq_region_name":"7","id":"rs899250535","source":"dbSNP","start":140439505,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140439505,"feature_type":"variation","strand":1},{"alleles":["T","A","C"],"end":140439513,"feature_type":"variation","strand":1,"source":"dbSNP","start":140439513,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs994962474","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439523,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140439523,"seq_region_name":"7","id":"rs2130201014","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs538258969","feature_type":"variation","strand":1,"end":140439525,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439525},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140439526,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439526,"source":"dbSNP","seq_region_name":"7","id":"rs1799816864","clinical_significance":[]},{"source":"dbSNP","start":140439527,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140439527,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1466130998"},{"seq_region_name":"7","id":"rs958721148","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439532,"source":"dbSNP","strand":1,"feature_type":"variation","end":140439532,"alleles":["A","G","T"]},{"feature_type":"variation","strand":1,"end":140439535,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439535,"clinical_significance":[],"seq_region_name":"7","id":"rs1196271538"},{"clinical_significance":[],"seq_region_name":"7","id":"rs984743028","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439539,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140439539},{"seq_region_name":"7","id":"rs2130201038","clinical_significance":[],"end":140439540,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140439540,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs909315029","clinical_significance":[],"alleles":["A","C","G"],"end":140439543,"strand":1,"feature_type":"variation","start":140439543,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439544,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140439544,"clinical_significance":[],"seq_region_name":"7","id":"rs1799817012"},{"seq_region_name":"7","id":"rs1799817036","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439545,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140439545},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439548,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140439548,"clinical_significance":[],"seq_region_name":"7","id":"rs1309408553"},{"clinical_significance":[],"id":"rs1463440966","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140439549,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439549},{"end":140439551,"alleles":["GG","G"],"strand":1,"feature_type":"variation","start":140439550,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1267464197","seq_region_name":"7","clinical_significance":[]},{"end":140439551,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140439551,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs940756568"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1348235674","end":140439561,"alleles":["CACCACC","CACC"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140439555,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"id":"rs1408731894","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140439560,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439560,"source":"dbSNP"},{"source":"dbSNP","start":140439564,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140439564,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs886630435","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1254374838","clinical_significance":[],"strand":1,"feature_type":"variation","end":140439565,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439565,"source":"dbSNP"},{"alleles":["T","A"],"end":140439568,"strand":1,"feature_type":"variation","start":140439568,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1008993077","clinical_significance":[]},{"seq_region_name":"7","id":"rs1232797481","clinical_significance":[],"start":140439569,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140439569,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1366265788","alleles":["T","C"],"end":140439571,"feature_type":"variation","strand":1,"source":"dbSNP","start":140439571,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"id":"rs1300199538","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140439573,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439573,"source":"dbSNP"},{"id":"rs1799817310","seq_region_name":"7","clinical_significance":[],"start":140439578,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","G"],"end":140439578,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1799817322","seq_region_name":"7","source":"dbSNP","start":140439583,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140439583,"feature_type":"variation","strand":1},{"alleles":["A","G"],"end":140439585,"feature_type":"variation","strand":1,"source":"dbSNP","start":140439585,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799817340"},{"seq_region_name":"7","id":"rs1293343657","clinical_significance":[],"end":140439590,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140439590,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439594,"source":"dbSNP","strand":1,"feature_type":"variation","end":140439595,"alleles":["AA","A"],"id":"rs1799817378","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1342217943","seq_region_name":"7","end":140439598,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140439598,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439599,"feature_type":"variation","strand":1,"end":140439599,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799817425"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439607,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140439607,"clinical_significance":[],"id":"rs1585447421","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1242462301","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439610,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140439610},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140439616,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439616,"source":"dbSNP","seq_region_name":"7","id":"rs1264638941","clinical_significance":[]},{"source":"dbSNP","start":140439617,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","-"],"end":140439617,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1335474712"},{"seq_region_name":"7","id":"rs1799817541","clinical_significance":[],"end":140439618,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140439618,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799817562","end":140439620,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140439620,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1036492203","seq_region_name":"7","source":"dbSNP","start":140439624,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140439624,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140439625,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140439625,"alleles":["A","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1339757185"},{"alleles":["T","C"],"end":140439626,"strand":1,"feature_type":"variation","start":140439626,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1019175927","clinical_significance":[]},{"source":"dbSNP","start":140439627,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140439627,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1170358176"},{"seq_region_name":"7","id":"rs923430138","clinical_significance":[],"start":140439628,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140439628,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140439632,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439632,"source":"dbSNP","seq_region_name":"7","id":"rs964953961","clinical_significance":[]},{"clinical_significance":[],"id":"rs1170207522","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140439634,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439634},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439638,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140439638,"clinical_significance":[],"id":"rs750788343","seq_region_name":"7"},{"alleles":["T","C"],"end":140439640,"strand":1,"feature_type":"variation","start":140439640,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1799817762","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1241351479","consequence_type":"TF_binding_site_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439640,"feature_type":"variation","strand":1,"end":140439642,"alleles":["TTT","TT"]},{"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140439646,"assembly_name":"GRCh38","consequence_type":"TF_binding_site_variant","start":140439646,"source":"dbSNP","seq_region_name":"7","id":"rs1482180788","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1204590399","end":140439648,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140439648,"consequence_type":"TF_binding_site_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140439650,"alleles":["G","A","T"],"consequence_type":"TF_binding_site_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439650,"clinical_significance":[],"seq_region_name":"7","id":"rs1799817864"},{"clinical_significance":[],"id":"rs1444127895","seq_region_name":"7","consequence_type":"TF_binding_site_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439654,"feature_type":"variation","strand":1,"end":140439654,"alleles":["C","A"]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439655,"source":"dbSNP","strand":1,"feature_type":"variation","end":140439655,"alleles":["T","C"],"id":"rs1254150501","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439662,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140439662,"clinical_significance":[],"seq_region_name":"7","id":"rs1199955458"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563080286","alleles":["AAAAAA","AAAAAAA"],"end":140439667,"feature_type":"variation","strand":1,"source":"dbSNP","start":140439662,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1256895507","seq_region_name":"7","source":"dbSNP","start":140439666,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140439666,"alleles":["A","T"],"feature_type":"variation","strand":1},{"id":"rs1799818012","seq_region_name":"7","clinical_significance":[],"start":140439676,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140439676,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1426109586","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140439678,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439678},{"seq_region_name":"7","id":"rs1226585382","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140439682,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439682,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799818068","feature_type":"variation","strand":1,"alleles":["AA","AAA"],"end":140439684,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439683},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140439685,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439685,"clinical_significance":[],"seq_region_name":"7","id":"rs1732472892"},{"start":140439687,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140439687,"strand":1,"feature_type":"variation","id":"rs1799818095","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799818121","seq_region_name":"7","source":"dbSNP","start":140439688,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140439688,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1799818146","seq_region_name":"7","end":140439692,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140439692,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140439693,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140439693,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799818169","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799818188","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140439696,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439696},{"clinical_significance":[],"id":"rs1799818210","seq_region_name":"7","feature_type":"variation","strand":1,"end":140439697,"alleles":["C","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439697},{"source":"dbSNP","start":140439700,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140439700,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1341860589"},{"seq_region_name":"7","id":"rs1799818246","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439701,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140439701},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140439703,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439703,"clinical_significance":[],"seq_region_name":"7","id":"rs1799818267"},{"clinical_significance":[],"seq_region_name":"7","id":"rs868841160","alleles":["C","A","G"],"end":140439705,"feature_type":"variation","strand":1,"source":"dbSNP","start":140439705,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"alleles":["C","T"],"end":140439711,"strand":1,"feature_type":"variation","start":140439711,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799818468","clinical_significance":[]},{"seq_region_name":"7","id":"rs1334670824","clinical_significance":[],"strand":1,"feature_type":"variation","end":140439713,"alleles":["AT","-"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439712,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1050741581","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439713,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140439713},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140439715,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439715,"clinical_significance":[],"seq_region_name":"7","id":"rs1799818789"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1032712522","alleles":["A","G"],"end":140439717,"feature_type":"variation","strand":1,"source":"dbSNP","start":140439717,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1585447502","clinical_significance":[],"start":140439723,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140439723,"alleles":["G","A","T"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140439724,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439724,"clinical_significance":[],"seq_region_name":"7","id":"rs957259960"},{"clinical_significance":[],"seq_region_name":"7","id":"rs766607167","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439725,"feature_type":"variation","strand":1,"end":140439725,"alleles":["G","A"]},{"id":"rs2130201314","seq_region_name":"7","clinical_significance":[],"start":140439727,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140439727,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1799818923","seq_region_name":"7","end":140439728,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140439728,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1799818946","clinical_significance":[],"start":140439733,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140439733,"strand":1,"feature_type":"variation"},{"start":140439738,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140439738,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1309451186","clinical_significance":[]},{"seq_region_name":"7","id":"rs1427462949","clinical_significance":[],"strand":1,"feature_type":"variation","end":140439758,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439758,"source":"dbSNP"},{"id":"rs912973895","seq_region_name":"7","clinical_significance":[],"start":140439762,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","C"],"end":140439762,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439764,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140439764,"seq_region_name":"7","id":"rs1450554095","clinical_significance":[]},{"id":"rs971232184","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140439769,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439769,"source":"dbSNP"},{"alleles":["T","G"],"end":140439770,"strand":1,"feature_type":"variation","start":140439770,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs529388768","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140439771,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439771,"clinical_significance":[],"id":"rs2130201334","seq_region_name":"7"},{"start":140439773,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","T"],"end":140439773,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1163681084","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1006592251","alleles":["G","T"],"end":140439774,"feature_type":"variation","strand":1,"source":"dbSNP","start":140439774,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1366649873","alleles":["A","C"],"end":140439775,"feature_type":"variation","strand":1,"source":"dbSNP","start":140439775,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1799819213","clinical_significance":[],"start":140439783,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140439783,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1368366980","clinical_significance":[],"strand":1,"feature_type":"variation","end":140439784,"alleles":["A","-"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439784,"source":"dbSNP"},{"id":"rs1799819297","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140439785,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439785,"source":"dbSNP"},{"end":140439792,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140439792,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1563080314","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140439806,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439806,"clinical_significance":[],"id":"rs1799819344","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1428650014","feature_type":"variation","strand":1,"end":140439809,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439809},{"start":140439823,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140439823,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799819395","clinical_significance":[]},{"seq_region_name":"7","id":"rs1302949585","clinical_significance":[],"strand":1,"feature_type":"variation","end":140439824,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439824,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["A","C","T"],"end":140439826,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439826,"source":"dbSNP","seq_region_name":"7","id":"rs1254133203","clinical_significance":[]},{"seq_region_name":"7","id":"rs1054097090","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140439828,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439828,"source":"dbSNP"},{"alleles":["T","G"],"end":140439829,"strand":1,"feature_type":"variation","start":140439829,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1482885298","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1290966376","feature_type":"variation","strand":1,"end":140439832,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439832},{"clinical_significance":[],"seq_region_name":"7","id":"rs143743640","alleles":["T","C"],"end":140439834,"feature_type":"variation","strand":1,"source":"dbSNP","start":140439834,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439836,"feature_type":"variation","strand":1,"end":140439836,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1354816996"},{"feature_type":"variation","strand":1,"end":140439842,"alleles":["AATAA","AA"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439838,"clinical_significance":[],"seq_region_name":"7","id":"rs1799819685"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1311989598","end":140439839,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140439839,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1229604483","source":"dbSNP","start":140439840,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140439840,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs754981055","source":"dbSNP","start":140439841,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140439841,"alleles":["A","G","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1350530794","alleles":["T","C"],"end":140439844,"feature_type":"variation","strand":1,"source":"dbSNP","start":140439844,"consequence_type":"TF_binding_site_variant","assembly_name":"GRCh38"},{"start":140439850,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"TF_binding_site_variant","end":140439850,"alleles":["G","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1289747780","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799820158","seq_region_name":"7","source":"dbSNP","start":140439853,"consequence_type":"TF_binding_site_variant","assembly_name":"GRCh38","end":140439853,"alleles":["A","G"],"feature_type":"variation","strand":1},{"id":"rs1585447561","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"TF_binding_site_variant","start":140439854,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140439854},{"alleles":["C","T"],"end":140439864,"feature_type":"variation","strand":1,"source":"dbSNP","start":140439864,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799820211","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799820229","clinical_significance":[],"end":140439872,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140439872,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439876,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140439876,"clinical_significance":[],"seq_region_name":"7","id":"rs1407599510"},{"alleles":["T","C","G"],"end":140439878,"feature_type":"variation","strand":1,"source":"dbSNP","start":140439878,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1326953011"},{"seq_region_name":"7","id":"rs1585447573","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439879,"source":"dbSNP","strand":1,"feature_type":"variation","end":140439879,"alleles":["T","G"]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439886,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","G","T"],"end":140439886,"seq_region_name":"7","id":"rs1230391849","clinical_significance":[]},{"start":140439888,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","TTAATCTCTTT"],"end":140439888,"strand":1,"feature_type":"variation","id":"rs1799820364","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799820385","feature_type":"variation","strand":1,"end":140439889,"alleles":["-","TA"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439890},{"alleles":["A","C"],"end":140439891,"strand":1,"feature_type":"variation","start":140439891,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1009953542","clinical_significance":[]},{"seq_region_name":"7","id":"rs1323889878","clinical_significance":[],"start":140439893,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["TCTTCTT","TCTT"],"end":140439899,"strand":1,"feature_type":"variation"},{"alleles":["T","G"],"end":140439895,"feature_type":"variation","strand":1,"source":"dbSNP","start":140439895,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130201442"},{"seq_region_name":"7","id":"rs1799821008","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140439897,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439897,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140439899,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439899,"clinical_significance":[],"seq_region_name":"7","id":"rs1799821034"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439900,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140439900,"seq_region_name":"7","id":"rs1020444264","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140439901,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439901,"source":"dbSNP","seq_region_name":"7","id":"rs28439514","clinical_significance":[]},{"alleles":["T","C"],"end":140439904,"feature_type":"variation","strand":1,"source":"dbSNP","start":140439904,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799821185","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1204654978","feature_type":"variation","strand":1,"end":140439905,"alleles":["A","C","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439905},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439906,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140439906,"seq_region_name":"7","id":"rs866697928","clinical_significance":[]},{"end":140439908,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140439908,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1585447594","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1472916513","source":"dbSNP","start":140439920,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140439920,"alleles":["C","G"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140439924,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","C","G"],"end":140439924,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs757423127"},{"end":140439925,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140439925,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799821334","clinical_significance":[]},{"seq_region_name":"7","id":"rs1414259051","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439929,"source":"dbSNP","strand":1,"feature_type":"variation","end":140439929,"alleles":["A","T"]},{"end":140439931,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140439931,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1799821378","seq_region_name":"7","clinical_significance":[]},{"start":140439933,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140439933,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799821406","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799821427","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140439942,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439942},{"source":"dbSNP","start":140439946,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140439946,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1034298399"},{"start":140439949,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140439949,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1038683253","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439950,"source":"dbSNP","strand":1,"feature_type":"variation","end":140439950,"alleles":["G","A"],"id":"rs539085336","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439951,"feature_type":"variation","strand":1,"end":140439951,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1465726098"},{"clinical_significance":[],"seq_region_name":"7","id":"rs749165537","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140439952,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439952},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439952,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GGTGG","GGTGGTGG"],"end":140439956,"seq_region_name":"7","id":"rs1224178645","clinical_significance":[]},{"end":140439956,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140439956,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs2130201536","clinical_significance":[]},{"seq_region_name":"7","id":"rs1209898414","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439960,"source":"dbSNP","strand":1,"feature_type":"variation","end":140439960,"alleles":["A","-"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs11767027","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439961,"feature_type":"variation","strand":1,"end":140439961,"alleles":["C","A","T"]},{"seq_region_name":"7","id":"rs551385136","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439962,"source":"dbSNP","strand":1,"feature_type":"variation","end":140439962,"alleles":["G","A","C"]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140439966,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439966,"source":"dbSNP","seq_region_name":"7","id":"rs1799821771","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1372107178","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439971,"feature_type":"variation","strand":1,"end":140439971,"alleles":["G","A","C"]},{"clinical_significance":[],"id":"rs1799821818","seq_region_name":"7","end":140439974,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140439974,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1799821831","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439978,"source":"dbSNP","strand":1,"feature_type":"variation","end":140439978,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1009025797","clinical_significance":[],"strand":1,"feature_type":"variation","end":140439983,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439983,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563080356","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439987,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140439987},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439988,"source":"dbSNP","strand":1,"feature_type":"variation","end":140439988,"alleles":["C","A"],"seq_region_name":"7","id":"rs1799821901","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799821926","seq_region_name":"7","alleles":["T","C"],"end":140439989,"feature_type":"variation","strand":1,"source":"dbSNP","start":140439989,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"end":140439991,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140439991,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799821946","clinical_significance":[]},{"id":"rs1040487992","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439992,"source":"dbSNP","strand":1,"feature_type":"variation","end":140439992,"alleles":["G","A"]},{"id":"rs1329105764","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140439994,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439994,"source":"dbSNP"},{"seq_region_name":"7","id":"rs900660575","clinical_significance":[],"strand":1,"feature_type":"variation","end":140439995,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439995,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585447636","feature_type":"variation","strand":1,"end":140439997,"alleles":["GGG","GGGGGG"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439995},{"seq_region_name":"7","id":"rs1799822040","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140439997,"source":"dbSNP","strand":1,"feature_type":"variation","end":140439997,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs996481972","clinical_significance":[],"start":140439998,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"TF_binding_site_variant","alleles":["C","G","T"],"end":140439998,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140439999,"alleles":["G","A"],"consequence_type":"TF_binding_site_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439999,"clinical_significance":[],"seq_region_name":"7","id":"rs1156984190"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799822121","feature_type":"variation","strand":1,"alleles":["GGATCACAAGGTCAGGA","GGA"],"end":140440015,"consequence_type":"TF_binding_site_variant","assembly_name":"GRCh38","source":"dbSNP","start":140439999},{"clinical_significance":[],"seq_region_name":"7","id":"rs1400219040","consequence_type":"TF_binding_site_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440001,"feature_type":"variation","strand":1,"end":140440001,"alleles":["A","C","G"]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140440002,"consequence_type":"TF_binding_site_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440002,"clinical_significance":[],"seq_region_name":"7","id":"rs1426026079"},{"alleles":["A","C"],"end":140440004,"feature_type":"variation","strand":1,"source":"dbSNP","start":140440004,"consequence_type":"TF_binding_site_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1193108468"},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140440014,"consequence_type":"TF_binding_site_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440014,"clinical_significance":[],"id":"rs182526020","seq_region_name":"7"},{"consequence_type":"TF_binding_site_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440017,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140440017,"clinical_significance":[],"seq_region_name":"7","id":"rs1252742538"},{"clinical_significance":[],"id":"rs2130201645","seq_region_name":"7","feature_type":"variation","strand":1,"end":140440019,"alleles":["C","T"],"consequence_type":"TF_binding_site_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440019},{"seq_region_name":"7","id":"rs1585447659","clinical_significance":[],"end":140440023,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140440023,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"strand":1,"feature_type":"variation","end":140440024,"alleles":["C","A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440024,"source":"dbSNP","seq_region_name":"7","id":"rs370145494","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799822301","source":"dbSNP","start":140440026,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140440026,"alleles":["A","C"],"feature_type":"variation","strand":1},{"end":140440027,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140440027,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1466585088","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140440032,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140440032,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1301723656"},{"clinical_significance":[],"id":"rs1585447672","seq_region_name":"7","alleles":["C","T"],"end":140440033,"feature_type":"variation","strand":1,"source":"dbSNP","start":140440033,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440038,"feature_type":"variation","strand":1,"end":140440038,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs972208656"},{"alleles":["T","C"],"end":140440039,"strand":1,"feature_type":"variation","start":140440039,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs957090060","clinical_significance":[]},{"start":140440041,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140440041,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1009876916","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140440042,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440042,"clinical_significance":[],"seq_region_name":"7","id":"rs28538447"},{"seq_region_name":"7","id":"rs1318331540","clinical_significance":[],"alleles":["C","T"],"end":140440047,"strand":1,"feature_type":"variation","start":140440047,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440050,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140440050,"clinical_significance":[],"seq_region_name":"7","id":"rs1364110531"},{"seq_region_name":"7","id":"rs1799822599","clinical_significance":[],"start":140440051,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140440051,"strand":1,"feature_type":"variation"},{"end":140440055,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140440055,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585447698"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799822658","feature_type":"variation","strand":1,"end":140440056,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440056},{"seq_region_name":"7","id":"rs1799822689","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440057,"source":"dbSNP","strand":1,"feature_type":"variation","end":140440061,"alleles":["ACTAA","ACTAACTAA"]},{"end":140440058,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140440058,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1342455719","seq_region_name":"7"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440059,"feature_type":"variation","strand":1,"end":140440059,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs971095677"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440064,"feature_type":"variation","strand":1,"end":140440064,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1288097459"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440072,"source":"dbSNP","strand":1,"feature_type":"variation","end":140440072,"alleles":["A","G"],"id":"rs1799822784","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1435586175","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440077,"feature_type":"variation","strand":1,"end":140440077,"alleles":["C","G"]},{"strand":1,"feature_type":"variation","alleles":["C","-"],"end":140440077,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440077,"source":"dbSNP","seq_region_name":"7","id":"rs1799822821","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585447707","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140440078,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440078},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440082,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140440082,"seq_region_name":"7","id":"rs1799822873","clinical_significance":[]},{"clinical_significance":[],"id":"rs1214219337","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440083,"feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140440083},{"clinical_significance":[],"id":"rs1302315178","seq_region_name":"7","feature_type":"variation","strand":1,"end":140440084,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440084},{"end":140440086,"alleles":["GG","G"],"strand":1,"feature_type":"variation","start":140440085,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1799822941","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1367213320","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440087,"feature_type":"variation","strand":1,"end":140440087,"alleles":["T","G"]},{"seq_region_name":"7","id":"rs981280928","clinical_significance":[],"start":140440088,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140440088,"strand":1,"feature_type":"variation"},{"start":140440090,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140440090,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1429989140","clinical_significance":[]},{"end":140440091,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","start":140440091,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1799823031","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140440094,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440094,"clinical_significance":[],"seq_region_name":"7","id":"rs927180824"},{"source":"dbSNP","start":140440095,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140440095,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs567804011"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440099,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140440099,"clinical_significance":[],"seq_region_name":"7","id":"rs745680820"},{"seq_region_name":"7","id":"rs185868472","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140440114,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440114,"source":"dbSNP"},{"seq_region_name":"7","id":"rs974038932","clinical_significance":[],"start":140440115,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A","T"],"end":140440115,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140440116,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440116,"clinical_significance":[],"seq_region_name":"7","id":"rs919823819"},{"id":"rs1246624481","seq_region_name":"7","clinical_significance":[],"start":140440124,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","C"],"end":140440124,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1799823260","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140440127,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440127,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140440127,"alleles":["T","TT"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440127,"source":"dbSNP","id":"rs1799823275","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440129,"source":"dbSNP","strand":1,"feature_type":"variation","end":140440129,"alleles":["G","A"],"seq_region_name":"7","id":"rs771810556","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799823318","clinical_significance":[],"start":140440137,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140440137,"alleles":["T","G"],"strand":1,"feature_type":"variation"},{"id":"rs1047682706","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440141,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140440141},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140440145,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440145,"source":"dbSNP","seq_region_name":"7","id":"rs910822397","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799823375","clinical_significance":[],"start":140440146,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140440146,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"start":140440148,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","C"],"end":140440148,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799823396","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799823411","seq_region_name":"7","source":"dbSNP","start":140440149,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140440149,"feature_type":"variation","strand":1},{"id":"rs1237497087","seq_region_name":"7","clinical_significance":[],"alleles":["A","G"],"end":140440150,"strand":1,"feature_type":"variation","start":140440150,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs868638912","clinical_significance":[],"strand":1,"feature_type":"variation","end":140440153,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440153,"source":"dbSNP"},{"end":140440154,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140440154,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs944829211"},{"source":"dbSNP","start":140440156,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140440156,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1464771141","seq_region_name":"7"},{"end":140440157,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140440157,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799823559"},{"start":140440158,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140440158,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799823583","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1040433880","end":140440160,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140440160,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"alleles":["A","G"],"end":140440163,"strand":1,"feature_type":"variation","start":140440163,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799823636","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440164,"source":"dbSNP","strand":1,"feature_type":"variation","end":140440164,"alleles":["G","C"],"seq_region_name":"7","id":"rs1293264373","clinical_significance":[]},{"source":"dbSNP","start":140440168,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140440168,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1213910942"},{"clinical_significance":[],"id":"rs1799823698","seq_region_name":"7","end":140440171,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140440171,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440172,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140440172,"clinical_significance":[],"seq_region_name":"7","id":"rs1799823726"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1379818939","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440174,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140440174},{"start":140440175,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140440175,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1269076709","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440176,"feature_type":"variation","strand":1,"end":140440176,"alleles":["C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799823792"},{"seq_region_name":"7","id":"rs553537266","clinical_significance":[],"start":140440178,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140440178,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs775255988","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440179,"feature_type":"variation","strand":1,"end":140440179,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799823873","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440182,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140440182},{"seq_region_name":"7","id":"rs1799823896","clinical_significance":[],"start":140440187,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140440187,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"end":140440198,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140440198,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1445950249"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799823939","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440205,"feature_type":"variation","strand":1,"end":140440205,"alleles":["G","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1375021091","alleles":["A","G"],"end":140440206,"feature_type":"variation","strand":1,"source":"dbSNP","start":140440206,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs945690843","clinical_significance":[],"start":140440207,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140440207,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1174775024","end":140440208,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140440208,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799824037","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440208,"feature_type":"variation","strand":1,"alleles":["C","CC"],"end":140440208},{"alleles":["A","G"],"end":140440209,"feature_type":"variation","strand":1,"source":"dbSNP","start":140440209,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1412014968","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140440212,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440212,"clinical_significance":[],"seq_region_name":"7","id":"rs1041491599"},{"seq_region_name":"7","id":"rs996736324","clinical_significance":[],"start":140440213,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","G","T"],"end":140440213,"strand":1,"feature_type":"variation"},{"start":140440213,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","CC"],"end":140440213,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1458756298","clinical_significance":[]},{"end":140440214,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140440214,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1585447779","seq_region_name":"7"},{"clinical_significance":[],"id":"rs2130201911","seq_region_name":"7","alleles":["A","-"],"end":140440217,"feature_type":"variation","strand":1,"source":"dbSNP","start":140440217,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140440224,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440224,"source":"dbSNP","seq_region_name":"7","id":"rs1002722010","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1424838754","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440226,"feature_type":"variation","strand":1,"end":140440226,"alleles":["A","C"]},{"seq_region_name":"7","id":"rs1416631613","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440228,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140440228},{"clinical_significance":[],"seq_region_name":"7","id":"rs1034575202","source":"dbSNP","start":140440229,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["AAAAAAAAA","AAAAAAAA","AAAAAAAAAA"],"end":140440237,"feature_type":"variation","strand":1},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440230,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140440230,"clinical_significance":[],"id":"rs1799824292","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140440232,"alleles":["A","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440232,"clinical_significance":[],"seq_region_name":"7","id":"rs894400611"},{"alleles":["A","G"],"end":140440234,"feature_type":"variation","strand":1,"source":"dbSNP","start":140440234,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1006060349"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440236,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140440236,"seq_region_name":"7","id":"rs1799824350","clinical_significance":[]},{"seq_region_name":"7","id":"rs746728819","clinical_significance":[],"start":140440238,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","A","G"],"end":140440238,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1799824402","clinical_significance":[],"end":140440239,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140440239,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140440244,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440244,"source":"dbSNP","id":"rs1799824430","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1437015211","clinical_significance":[],"end":140440245,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140440245,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1585447800","clinical_significance":[],"end":140440248,"alleles":["GG","G"],"strand":1,"feature_type":"variation","start":140440247,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1799824504","clinical_significance":[],"strand":1,"feature_type":"variation","end":140440248,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440248,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799824532","clinical_significance":[],"alleles":["G","A"],"end":140440251,"strand":1,"feature_type":"variation","start":140440251,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1016127198","clinical_significance":[],"strand":1,"feature_type":"variation","end":140440256,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440256,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs962060591","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440258,"feature_type":"variation","strand":1,"end":140440258,"alleles":["C","T"]},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140440259,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440259,"source":"dbSNP","id":"rs972458537","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799824698","seq_region_name":"7","alleles":["A","G"],"end":140440274,"feature_type":"variation","strand":1,"source":"dbSNP","start":140440274,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440277,"feature_type":"variation","strand":1,"end":140440283,"alleles":["TAATTAA","TAA"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799824717"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440280,"feature_type":"variation","strand":1,"end":140440280,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130201972"},{"source":"dbSNP","start":140440284,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140440284,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130201979"},{"start":140440290,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140440290,"alleles":["C","A"],"strand":1,"feature_type":"variation","id":"rs1799824740","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1314794686","clinical_significance":[],"start":140440292,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140440292,"strand":1,"feature_type":"variation"},{"id":"rs542834744","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440293,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140440293},{"seq_region_name":"7","id":"rs572125503","clinical_significance":[],"end":140440298,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140440298,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140440299,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440299,"source":"dbSNP","seq_region_name":"7","id":"rs1799824846","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs768040336","alleles":["A","G"],"end":140440305,"feature_type":"variation","strand":1,"source":"dbSNP","start":140440305,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"id":"rs986317399","seq_region_name":"7","clinical_significance":[],"start":140440310,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140440310,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140440313,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140440313,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799824920"},{"alleles":["G","A","T"],"end":140440318,"feature_type":"variation","strand":1,"source":"dbSNP","start":140440318,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs910688355"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140440319,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440319,"source":"dbSNP","seq_region_name":"7","id":"rs776275308","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140440321,"alleles":["C","A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440321,"clinical_significance":[],"id":"rs1799825022","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799825050","clinical_significance":[],"strand":1,"feature_type":"variation","end":140440329,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440329,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799825070","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440333,"source":"dbSNP","strand":1,"feature_type":"variation","end":140440333,"alleles":["C","T"]},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140440335,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440335,"source":"dbSNP","seq_region_name":"7","id":"rs114948525","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1458757167","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440336,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140440336},{"clinical_significance":[],"id":"rs1799825161","seq_region_name":"7","end":140440344,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140440344,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1352033984","source":"dbSNP","start":140440347,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140440347,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140440350,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140440350,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1329866198","seq_region_name":"7"},{"end":140440356,"alleles":["TTTT","TTTTT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140440353,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs936812618"},{"end":140440359,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140440359,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799825287","clinical_significance":[]},{"clinical_significance":[],"id":"rs1416512745","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440362,"feature_type":"variation","strand":1,"end":140440362,"alleles":["G","A"]},{"id":"rs1585447838","seq_region_name":"7","clinical_significance":[],"end":140440363,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140440363,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs2130202068","clinical_significance":[],"end":140440366,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140440366,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"id":"rs989767772","seq_region_name":"7","alleles":["G","A","T"],"end":140440368,"feature_type":"variation","strand":1,"source":"dbSNP","start":140440368,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140440370,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440370,"source":"dbSNP","seq_region_name":"7","id":"rs1799825386","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799825409","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440370,"feature_type":"variation","strand":1,"end":140440372,"alleles":["GGG","GG"]},{"source":"dbSNP","start":140440373,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","AA"],"end":140440373,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs34789976"},{"strand":1,"feature_type":"variation","end":140440373,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440373,"source":"dbSNP","id":"rs1473328007","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140440375,"alleles":["G","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440375,"clinical_significance":[],"seq_region_name":"7","id":"rs1799825476"},{"alleles":["T","C"],"end":140440377,"strand":1,"feature_type":"variation","start":140440377,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1019927534","clinical_significance":[]},{"start":140440399,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140440399,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1230283002","clinical_significance":[]},{"seq_region_name":"7","id":"rs1266851698","clinical_significance":[],"strand":1,"feature_type":"variation","end":140440400,"alleles":["A","G","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440400,"source":"dbSNP"},{"seq_region_name":"7","id":"rs914138174","clinical_significance":[],"start":140440404,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140440404,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799825619","feature_type":"variation","strand":1,"end":140440415,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440415},{"start":140440416,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140440416,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs906857388","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs945760361","clinical_significance":[],"start":140440417,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140440417,"alleles":["G","A","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1268777209","source":"dbSNP","start":140440420,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["AAAA","AAA"],"end":140440423,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1799825719","seq_region_name":"7","feature_type":"variation","strand":1,"end":140440431,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440431},{"source":"dbSNP","start":140440436,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140440436,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs115513466"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440439,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140440439,"clinical_significance":[],"seq_region_name":"7","id":"rs1799825785"},{"start":140440443,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140440443,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1334157746","clinical_significance":[]},{"source":"dbSNP","start":140440445,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140440445,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799825824"},{"strand":1,"feature_type":"variation","end":140440447,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440447,"source":"dbSNP","id":"rs1799825842","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140440448,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440448,"clinical_significance":[],"seq_region_name":"7","id":"rs1034493987"},{"alleles":["G","A"],"end":140440454,"strand":1,"feature_type":"variation","start":140440454,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1387606150","clinical_significance":[]},{"seq_region_name":"7","id":"rs906969706","clinical_significance":[],"strand":1,"feature_type":"variation","end":140440455,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440455,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799825938","source":"dbSNP","start":140440463,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140440463,"alleles":["G","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1190207445","clinical_significance":[],"end":140440465,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140440465,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs938392707","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440466,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140440466},{"seq_region_name":"7","id":"rs958592671","clinical_significance":[],"strand":1,"feature_type":"variation","end":140440468,"alleles":["T","A","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440468,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1390017541","clinical_significance":[],"alleles":["T","TT"],"end":140440468,"strand":1,"feature_type":"variation","start":140440468,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"alleles":["C","T"],"end":140440470,"feature_type":"variation","strand":1,"source":"dbSNP","start":140440470,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs894347941"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1473321454","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440471,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140440471},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130202186","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440485,"feature_type":"variation","strand":1,"end":140440485,"alleles":["A","C"]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440488,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140440488,"seq_region_name":"7","id":"rs56093957","clinical_significance":[]},{"seq_region_name":"7","id":"rs1411213069","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440489,"source":"dbSNP","strand":1,"feature_type":"variation","end":140440489,"alleles":["G","A"]},{"source":"dbSNP","start":140440495,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140440495,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799826208"},{"clinical_significance":[],"seq_region_name":"7","id":"rs6975307","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440496,"feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140440496},{"start":140440497,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140440497,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs951267987","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs982657788","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140440499,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440499},{"id":"rs2130202230","seq_region_name":"7","clinical_significance":[],"alleles":["C","G"],"end":140440501,"strand":1,"feature_type":"variation","start":140440501,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799826382","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440503,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140440503},{"alleles":["G","A"],"end":140440504,"strand":1,"feature_type":"variation","start":140440504,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1248593390","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799826426","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["GG","G"],"end":140440507,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440506,"source":"dbSNP"},{"alleles":["C","G"],"end":140440510,"feature_type":"variation","strand":1,"source":"dbSNP","start":140440510,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799826449"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799826475","end":140440516,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140440516,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140440520,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140440520,"alleles":["T","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585447948"},{"seq_region_name":"7","id":"rs1799826526","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440523,"source":"dbSNP","strand":1,"feature_type":"variation","end":140440523,"alleles":["G","C"]},{"feature_type":"variation","strand":1,"end":140440524,"alleles":["A","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440524,"clinical_significance":[],"seq_region_name":"7","id":"rs907920501"},{"start":140440529,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140440529,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1347834747","clinical_significance":[]},{"seq_region_name":"7","id":"rs1348592095","clinical_significance":[],"strand":1,"feature_type":"variation","end":140440531,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440531,"source":"dbSNP"},{"source":"dbSNP","start":140440540,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140440540,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799826604","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799826633","clinical_significance":[],"end":140440542,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140440542,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"source":"dbSNP","start":140440548,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140440548,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1030725831"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585447965","feature_type":"variation","strand":1,"end":140440552,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440552},{"source":"dbSNP","start":140440555,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140440555,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1234223658"},{"end":140440556,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140440556,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799826734"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440560,"feature_type":"variation","strand":1,"end":140440560,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799826755"},{"alleles":["C","T"],"end":140440562,"feature_type":"variation","strand":1,"source":"dbSNP","start":140440562,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799826780"},{"seq_region_name":"7","id":"rs1585447976","clinical_significance":[],"start":140440563,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140440563,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs190931555","feature_type":"variation","strand":1,"alleles":["A","T"],"end":140440566,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440566},{"id":"rs2130202337","seq_region_name":"7","clinical_significance":[],"end":140440568,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140440568,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799826837","source":"dbSNP","start":140440572,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140440572,"feature_type":"variation","strand":1},{"start":140440574,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140440574,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585447985","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140440623,"alleles":["AGAGTGAGACCTTCTCTCAAAAAAAAAAAAAAAAAAAAAAAAAAAG","AG"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440578,"clinical_significance":[],"id":"rs1799826890","seq_region_name":"7"},{"alleles":["G","A"],"end":140440579,"feature_type":"variation","strand":1,"source":"dbSNP","start":140440579,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799826916"},{"source":"dbSNP","start":140440581,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140440581,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130202356"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440582,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140440582,"seq_region_name":"7","id":"rs1585447988","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140440583,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440583,"source":"dbSNP","seq_region_name":"7","id":"rs1799826961","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799826990","feature_type":"variation","strand":1,"end":140440584,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440584},{"clinical_significance":[],"seq_region_name":"7","id":"rs561913121","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440585,"feature_type":"variation","strand":1,"alleles":["G","C","T"],"end":140440585},{"clinical_significance":[],"seq_region_name":"7","id":"rs1440662857","source":"dbSNP","start":140440587,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140440587,"alleles":["C","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130202377","alleles":["CT","-"],"end":140440589,"feature_type":"variation","strand":1,"source":"dbSNP","start":140440588,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140440588,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["CTTCT","CT"],"end":140440592,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1017696460"},{"id":"rs1323109219","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440589,"source":"dbSNP","strand":1,"feature_type":"variation","end":140440589,"alleles":["T","G"]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440590,"feature_type":"variation","strand":1,"end":140440590,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1411784141"},{"end":140440591,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140440591,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs2130202400","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799827151","source":"dbSNP","start":140440592,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","A","C"],"end":140440592,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs2130202408","seq_region_name":"7","source":"dbSNP","start":140440592,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140440592,"alleles":["T","TGT"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["C","-"],"end":140440593,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440593,"source":"dbSNP","seq_region_name":"7","id":"rs1799827177","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130202415","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140440593,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440593,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1382132582","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","-"],"end":140440594,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440594},{"seq_region_name":"7","id":"rs1585448015","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140440594,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440594,"source":"dbSNP"},{"end":140440596,"alleles":["TCA","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140440594,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1157543605"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440595,"feature_type":"variation","strand":1,"alleles":["-","A"],"end":140440594,"clinical_significance":[],"seq_region_name":"7","id":"rs1799827251"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440595,"feature_type":"variation","strand":1,"end":140440595,"alleles":["C","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1453551620"},{"strand":1,"feature_type":"variation","alleles":["C","-"],"end":140440595,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440595,"source":"dbSNP","seq_region_name":"7","id":"rs1466179390","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440595,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CA","-"],"end":140440596,"id":"rs1563080490","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1396540291","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440595,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CAA","-"],"end":140440597},{"end":140440598,"alleles":["CAAA","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140440595,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799827358"},{"id":"rs1171470514","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440595,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CAAAA","-"],"end":140440599},{"start":140440595,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140440600,"alleles":["CAAAAA","-"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799827407","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799827429","end":140440601,"alleles":["CAAAAAA","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140440595,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1563080493","clinical_significance":[],"end":140440609,"alleles":["CAAAAAAAAAAAAAA","-"],"strand":1,"feature_type":"variation","start":140440595,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"source":"dbSNP","start":140440596,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140440596,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799827463"},{"seq_region_name":"7","id":"rs57285148","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440596,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAA","AAAAAAAAAAA","AAAAAAAAAAAA","AAAAAAAAAAAAA","AAAAAAAAAAAAAA","AAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA"],"end":140440622},{"seq_region_name":"7","id":"rs1799827764","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440597,"source":"dbSNP","strand":1,"feature_type":"variation","end":140440597,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs958214235","clinical_significance":[],"alleles":["A","C","G"],"end":140440601,"strand":1,"feature_type":"variation","start":140440601,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799827822","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440602,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140440602},{"clinical_significance":[],"seq_region_name":"7","id":"rs1373281638","source":"dbSNP","start":140440605,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140440605,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799827874","alleles":["A","G"],"end":140440609,"feature_type":"variation","strand":1,"source":"dbSNP","start":140440609,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1229356833","end":140440619,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140440619,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440621,"feature_type":"variation","strand":1,"end":140440621,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs77809448"},{"clinical_significance":[],"id":"rs1799827934","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["AAG","-"],"end":140440623,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440621},{"clinical_significance":[],"id":"rs1372459178","seq_region_name":"7","alleles":["A","G"],"end":140440622,"feature_type":"variation","strand":1,"source":"dbSNP","start":140440622,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440622,"feature_type":"variation","strand":1,"alleles":["AG","-"],"end":140440623,"clinical_significance":[],"seq_region_name":"7","id":"rs1799827982"},{"source":"dbSNP","start":140440623,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140440623,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs74382856"},{"id":"rs146195933","seq_region_name":"7","clinical_significance":[],"start":140440623,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140440623,"alleles":["G","-"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1315281641","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["GC","-"],"end":140440624,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440623,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799828032","end":140440624,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140440624,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140440625,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440625,"source":"dbSNP","seq_region_name":"7","id":"rs1799828057","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["AAA","AAAAAAAA"],"end":140440627,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440625,"source":"dbSNP","seq_region_name":"7","id":"rs1799828076","clinical_significance":[]},{"end":140440628,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140440628,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1222198008","clinical_significance":[]},{"id":"rs1799828127","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440628,"source":"dbSNP","strand":1,"feature_type":"variation","end":140440637,"alleles":["GCTCTTTATG","GCTCTTTATGGCTCTTTATG"]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440630,"feature_type":"variation","strand":1,"end":140440630,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799828209"},{"seq_region_name":"7","id":"rs976222439","clinical_significance":[],"strand":1,"feature_type":"variation","end":140440631,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440631,"source":"dbSNP"},{"end":140440632,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140440632,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1585448070","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440636,"feature_type":"variation","strand":1,"end":140440636,"alleles":["T","C"],"clinical_significance":[],"id":"rs921982738","seq_region_name":"7"},{"end":140440638,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140440638,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799828314","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440644,"source":"dbSNP","strand":1,"feature_type":"variation","end":140440644,"alleles":["C","T"],"id":"rs1277143522","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1194442319","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440645,"feature_type":"variation","strand":1,"end":140440645,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1339247738","clinical_significance":[],"end":140440647,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140440647,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440649,"feature_type":"variation","strand":1,"end":140440649,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1285278733"},{"feature_type":"variation","strand":1,"end":140440650,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440650,"clinical_significance":[],"seq_region_name":"7","id":"rs1585448090"},{"alleles":["G","A"],"end":140440651,"feature_type":"variation","strand":1,"source":"dbSNP","start":140440651,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1247674894"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799828446","feature_type":"variation","strand":1,"end":140440652,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440652},{"id":"rs1356809089","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440655,"source":"dbSNP","strand":1,"feature_type":"variation","end":140440655,"alleles":["C","A","T"]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440658,"feature_type":"variation","strand":1,"end":140440658,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799828483"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440659,"source":"dbSNP","strand":1,"feature_type":"variation","end":140440659,"alleles":["A","G"],"seq_region_name":"7","id":"rs1413721235","clinical_significance":[]},{"end":140440660,"alleles":["T","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140440660,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs932186700"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140440661,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440661,"clinical_significance":[],"seq_region_name":"7","id":"rs1799829023"},{"source":"dbSNP","start":140440666,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140440666,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799829040"},{"end":140440669,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140440669,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1330588243","clinical_significance":[]},{"source":"dbSNP","start":140440671,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140440671,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs989634053"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440674,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140440674,"clinical_significance":[],"id":"rs2130202685","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799829099","end":140440681,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140440681,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs182263082","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440687,"feature_type":"variation","strand":1,"end":140440687,"alleles":["C","A"]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440690,"source":"dbSNP","strand":1,"feature_type":"variation","end":140440690,"alleles":["T","G"],"seq_region_name":"7","id":"rs1395574121","clinical_significance":[]},{"alleles":["C","A"],"end":140440694,"feature_type":"variation","strand":1,"source":"dbSNP","start":140440694,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1163743963"},{"clinical_significance":[],"seq_region_name":"7","id":"rs541224569","source":"dbSNP","start":140440697,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140440697,"alleles":["T","C"],"feature_type":"variation","strand":1},{"id":"rs1799829195","seq_region_name":"7","clinical_significance":[],"start":140440699,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","-"],"end":140440699,"strand":1,"feature_type":"variation"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440702,"feature_type":"variation","strand":1,"end":140440702,"alleles":["C","T"],"clinical_significance":[],"id":"rs1415754796","seq_region_name":"7"},{"end":140440711,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140440711,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1202435198","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440716,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140440716,"id":"rs1054991433","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140440717,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440717,"source":"dbSNP","seq_region_name":"7","id":"rs1234845340","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440721,"feature_type":"variation","strand":1,"end":140440721,"alleles":["G","A","T"],"clinical_significance":[],"id":"rs1473087879","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs893396211","feature_type":"variation","strand":1,"end":140440723,"alleles":["T","A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440723},{"clinical_significance":[],"id":"rs946315537","seq_region_name":"7","source":"dbSNP","start":140440724,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140440724,"alleles":["C","T"],"feature_type":"variation","strand":1},{"start":140440728,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140440728,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1041987577","clinical_significance":[]},{"end":140440732,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140440732,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs2130202754","clinical_significance":[]},{"id":"rs1437577055","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440734,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140440734},{"id":"rs1799829374","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140440735,"alleles":["A","C","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440735,"source":"dbSNP"},{"clinical_significance":[],"id":"rs559567230","seq_region_name":"7","alleles":["G","C","T"],"end":140440737,"feature_type":"variation","strand":1,"source":"dbSNP","start":140440737,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1585448140","clinical_significance":[],"start":140440740,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140440740,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"alleles":["C","T"],"end":140440747,"feature_type":"variation","strand":1,"source":"dbSNP","start":140440747,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130202774"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799829421","alleles":["T","C"],"end":140440748,"feature_type":"variation","strand":1,"source":"dbSNP","start":140440748,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140440753,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440753,"clinical_significance":[],"seq_region_name":"7","id":"rs1799829434"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1212136571","source":"dbSNP","start":140440756,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140440756,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs906889940","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140440761,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440761},{"clinical_significance":[],"id":"rs1270655713","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440762,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140440762},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440763,"source":"dbSNP","strand":1,"feature_type":"variation","end":140440768,"alleles":["TCTCTT","T"],"seq_region_name":"7","id":"rs928255526","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440764,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140440764,"clinical_significance":[],"id":"rs1350670469","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440767,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140440767,"seq_region_name":"7","id":"rs1168955484","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440767,"feature_type":"variation","strand":1,"end":140440768,"alleles":["TT","-"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799829608"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440769,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140440769,"clinical_significance":[],"seq_region_name":"7","id":"rs1799829625"},{"clinical_significance":[],"id":"rs1799829642","seq_region_name":"7","source":"dbSNP","start":140440772,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140440772,"alleles":["A","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1371452443","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140440778,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440778},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440779,"feature_type":"variation","strand":1,"end":140440779,"alleles":["T","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs938352574"},{"clinical_significance":[],"id":"rs576298568","seq_region_name":"7","feature_type":"variation","strand":1,"end":140440783,"alleles":["G","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440783},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799829738","alleles":["C","A"],"end":140440793,"feature_type":"variation","strand":1,"source":"dbSNP","start":140440793,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140440803,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440803,"clinical_significance":[],"seq_region_name":"7","id":"rs56769703"},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140440809,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440809,"source":"dbSNP","seq_region_name":"7","id":"rs1034115168","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440812,"source":"dbSNP","strand":1,"feature_type":"variation","end":140440812,"alleles":["G","A"],"seq_region_name":"7","id":"rs915644482","clinical_significance":[]},{"source":"dbSNP","start":140440813,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140440813,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs894178656","seq_region_name":"7"},{"start":140440813,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140440815,"alleles":["TTT","TTTT"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1462897922","clinical_significance":[]},{"clinical_significance":[],"id":"rs1164251704","seq_region_name":"7","source":"dbSNP","start":140440816,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140440816,"feature_type":"variation","strand":1},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440817,"feature_type":"variation","strand":1,"alleles":["TTTTTTT","TTTTTT"],"end":140440823,"clinical_significance":[],"seq_region_name":"7","id":"rs1799829968"},{"clinical_significance":[],"seq_region_name":"7","id":"rs551338487","end":140440825,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140440825,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1410307679","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440827,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["ACACA","ACA"],"end":140440831},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799830054","source":"dbSNP","start":140440831,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140440831,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799830070","source":"dbSNP","start":140440832,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140440832,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799830089","source":"dbSNP","start":140440833,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140440833,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1305171265","alleles":["T","G"],"end":140440835,"feature_type":"variation","strand":1,"source":"dbSNP","start":140440835,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140440837,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440837,"source":"dbSNP","id":"rs1799830127","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs941900029","clinical_significance":[],"start":140440842,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140440842,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs62490426","clinical_significance":[],"start":140440848,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140440848,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140440850,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440850,"clinical_significance":[],"seq_region_name":"7","id":"rs1799830187"},{"strand":1,"feature_type":"variation","end":140440859,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440859,"source":"dbSNP","id":"rs1037470625","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140440860,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440860,"clinical_significance":[],"seq_region_name":"7","id":"rs1799830242"},{"id":"rs57011646","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440865,"source":"dbSNP","strand":1,"feature_type":"variation","end":140440865,"alleles":["G","A"]},{"id":"rs1799830275","seq_region_name":"7","clinical_significance":[],"alleles":["A","G"],"end":140440868,"strand":1,"feature_type":"variation","start":140440868,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"alleles":["A","C"],"end":140440871,"strand":1,"feature_type":"variation","start":140440871,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs897762640","clinical_significance":[]},{"seq_region_name":"7","id":"rs563387822","clinical_significance":[],"end":140440880,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140440880,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1027269167","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440882,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140440882},{"seq_region_name":"7","id":"rs1799830365","clinical_significance":[],"alleles":["G","A"],"end":140440884,"strand":1,"feature_type":"variation","start":140440884,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs61344956","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440885,"source":"dbSNP","strand":1,"feature_type":"variation","end":140440885,"alleles":["G","C"]},{"seq_region_name":"7","id":"rs1799830404","clinical_significance":[],"end":140440886,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140440886,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"source":"dbSNP","start":140440888,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140440888,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs993785940"},{"id":"rs1245754545","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140440889,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440889,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440891,"source":"dbSNP","strand":1,"feature_type":"variation","end":140440891,"alleles":["C","T"],"seq_region_name":"7","id":"rs1799830442","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799830462","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440892,"source":"dbSNP","strand":1,"feature_type":"variation","end":140440892,"alleles":["T","A"]},{"start":140440894,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140440894,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799830483","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440896,"feature_type":"variation","strand":1,"end":140440896,"alleles":["T","A"],"clinical_significance":[],"id":"rs1252941974","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799830531","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140440897,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440897},{"clinical_significance":[],"seq_region_name":"7","id":"rs1051678375","source":"dbSNP","start":140440898,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140440898,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140440902,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440902,"source":"dbSNP","seq_region_name":"7","id":"rs61529872","clinical_significance":[]},{"start":140440903,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140440903,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs60259728","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440908,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140440908,"clinical_significance":[],"seq_region_name":"7","id":"rs951217207"},{"alleles":["C","G","T"],"end":140440909,"feature_type":"variation","strand":1,"source":"dbSNP","start":140440909,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs61675208","seq_region_name":"7"},{"alleles":["G","A"],"end":140440910,"strand":1,"feature_type":"variation","start":140440910,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs982687248","clinical_significance":[]},{"end":140440918,"alleles":["TTCTTCT","TTCT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140440912,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1349523281","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440914,"source":"dbSNP","strand":1,"feature_type":"variation","end":140440914,"alleles":["C","A","G"],"seq_region_name":"7","id":"rs561130619","clinical_significance":[]},{"seq_region_name":"7","id":"rs56919838","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140440916,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440916,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799830762","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440919,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140440919},{"feature_type":"variation","strand":1,"end":140440924,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440924,"clinical_significance":[],"seq_region_name":"7","id":"rs59213800"},{"seq_region_name":"7","id":"rs890489849","clinical_significance":[],"alleles":["C","T"],"end":140440927,"strand":1,"feature_type":"variation","start":140440927,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"start":140440929,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140440929,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799830830","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140440931,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440931,"clinical_significance":[],"seq_region_name":"7","id":"rs1442548164"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440932,"source":"dbSNP","strand":1,"feature_type":"variation","end":140440932,"alleles":["G","A"],"seq_region_name":"7","id":"rs56394119","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440934,"feature_type":"variation","strand":1,"end":140440934,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs548283638"},{"id":"rs2130203108","seq_region_name":"7","clinical_significance":[],"start":140440937,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140440937,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1347024347","clinical_significance":[],"alleles":["C","A","G"],"end":140440946,"strand":1,"feature_type":"variation","start":140440946,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"source":"dbSNP","start":140440947,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140440947,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799830968"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1316328779","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440950,"feature_type":"variation","strand":1,"end":140440950,"alleles":["G","A","T"]},{"alleles":["G","T"],"end":140440952,"feature_type":"variation","strand":1,"source":"dbSNP","start":140440952,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799831019"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440953,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140440953,"seq_region_name":"7","id":"rs922041175","clinical_significance":[]},{"seq_region_name":"7","id":"rs1175862752","clinical_significance":[],"alleles":["G","A"],"end":140440954,"strand":1,"feature_type":"variation","start":140440954,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1799831079","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140440956,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440956,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140440959,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440959,"clinical_significance":[],"id":"rs1799831103","seq_region_name":"7"},{"id":"rs1452935437","seq_region_name":"7","clinical_significance":[],"end":140440960,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140440960,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1585448312","clinical_significance":[],"start":140440965,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140440965,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"id":"rs1799831169","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140440971,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440971,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563080618","source":"dbSNP","start":140440972,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["AAA","A"],"end":140440974,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs932024465","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440975,"feature_type":"variation","strand":1,"end":140440975,"alleles":["G","T"]},{"seq_region_name":"7","id":"rs1189774798","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440982,"source":"dbSNP","strand":1,"feature_type":"variation","end":140440987,"alleles":["TTTTTT","TTTTTTT"]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140440990,"feature_type":"variation","strand":1,"end":140440994,"alleles":["AGAGA","AGA"],"clinical_significance":[],"seq_region_name":"7","id":"rs1460797849"},{"start":140440992,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140440992,"alleles":["A","G"],"strand":1,"feature_type":"variation","id":"rs567950187","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140440993,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440993,"source":"dbSNP","seq_region_name":"7","id":"rs1799831315","clinical_significance":[]},{"seq_region_name":"7","id":"rs1213044406","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","-"],"end":140440996,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140440996,"source":"dbSNP"},{"start":140440996,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140440996,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799831333","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs563393588","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441000,"feature_type":"variation","strand":1,"end":140441000,"alleles":["T","G"]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140441003,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441003,"source":"dbSNP","seq_region_name":"7","id":"rs1585448341","clinical_significance":[]},{"source":"dbSNP","start":140441005,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140441005,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799831416"},{"start":140441008,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","G"],"end":140441008,"strand":1,"feature_type":"variation","id":"rs958080429","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441010,"source":"dbSNP","strand":1,"feature_type":"variation","end":140441011,"alleles":["TT","T"],"id":"rs1799831470","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585448345","clinical_significance":[],"start":140441011,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140441011,"alleles":["T","G"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441017,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140441017,"id":"rs1236093073","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441019,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140441019,"id":"rs1345462715","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1302480769","clinical_significance":[],"end":140441021,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140441021,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1228976076","alleles":["G","T"],"end":140441022,"feature_type":"variation","strand":1,"source":"dbSNP","start":140441022,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"id":"rs1363991698","seq_region_name":"7","clinical_significance":[],"end":140441027,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140441027,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"end":140441029,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140441029,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1585448355","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140441036,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441036,"clinical_significance":[],"seq_region_name":"7","id":"rs1585448363"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1451569916","alleles":["A","G"],"end":140441042,"feature_type":"variation","strand":1,"source":"dbSNP","start":140441042,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441044,"source":"dbSNP","strand":1,"feature_type":"variation","end":140441044,"alleles":["T","C"],"id":"rs1585448369","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799832097","end":140441045,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140441045,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"id":"rs1585448372","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441047,"source":"dbSNP","strand":1,"feature_type":"variation","end":140441047,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1166889221","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441049,"source":"dbSNP","strand":1,"feature_type":"variation","end":140441049,"alleles":["C","T"]},{"feature_type":"variation","strand":1,"end":140441050,"alleles":["G","A","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441050,"clinical_significance":[],"seq_region_name":"7","id":"rs914780147"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1011096047","source":"dbSNP","start":140441052,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140441052,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1799832224","seq_region_name":"7","feature_type":"variation","strand":1,"end":140441053,"alleles":["T","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441053},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441058,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140441058,"clinical_significance":[],"seq_region_name":"7","id":"rs2130203278"},{"id":"rs1799832254","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441061,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140441061},{"clinical_significance":[],"id":"rs562102480","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140441064,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441064},{"start":140441068,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140441068,"strand":1,"feature_type":"variation","id":"rs966996102","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs547186678","end":140441081,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140441081,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441082,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140441082,"seq_region_name":"7","id":"rs1716363774","clinical_significance":[]},{"alleles":["C","T"],"end":140441084,"strand":1,"feature_type":"variation","start":140441084,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1799832373","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1375211642","clinical_significance":[],"end":140441085,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140441085,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441086,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140441086,"clinical_significance":[],"seq_region_name":"7","id":"rs1042018822"},{"seq_region_name":"7","id":"rs62490427","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441090,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140441090},{"clinical_significance":[],"seq_region_name":"7","id":"rs386718462","source":"dbSNP","start":140441090,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["TG","CA"],"end":140441091,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs114823661","source":"dbSNP","start":140441091,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140441091,"alleles":["G","A"],"feature_type":"variation","strand":1},{"start":140441092,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140441092,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1418032284","clinical_significance":[]},{"end":140441103,"alleles":["AAAAA","AAAA"],"strand":1,"feature_type":"variation","start":140441099,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799832584","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140441103,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441103,"source":"dbSNP","id":"rs1799832603","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1563080655","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140441114,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441114},{"seq_region_name":"7","id":"rs2130203362","clinical_significance":[],"alleles":["A","G"],"end":140441115,"strand":1,"feature_type":"variation","start":140441115,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799832643","source":"dbSNP","start":140441118,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140441126,"alleles":["ACACACACA","ACACACA","ACACACACACA"],"feature_type":"variation","strand":1},{"id":"rs1452495126","seq_region_name":"7","clinical_significance":[],"start":140441120,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140441120,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1321646920","source":"dbSNP","start":140441121,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140441121,"alleles":["C","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1563080656","seq_region_name":"7","alleles":["C","T"],"end":140441123,"feature_type":"variation","strand":1,"source":"dbSNP","start":140441123,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs747691280","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140441130,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441130},{"source":"dbSNP","start":140441131,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140441131,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1257686114"},{"alleles":["C","G","T"],"end":140441135,"feature_type":"variation","strand":1,"source":"dbSNP","start":140441135,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs557785605","seq_region_name":"7"},{"source":"dbSNP","start":140441136,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140441136,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1055836230"},{"clinical_significance":[],"id":"rs1799832864","seq_region_name":"7","feature_type":"variation","strand":1,"end":140441137,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441137},{"clinical_significance":[],"id":"rs1433329749","seq_region_name":"7","end":140441138,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140441138,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"alleles":["C","T"],"end":140441143,"strand":1,"feature_type":"variation","start":140441143,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799833133","clinical_significance":[]},{"end":140441147,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140441147,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1269295385","clinical_significance":[]},{"id":"rs185314558","seq_region_name":"7","clinical_significance":[],"end":140441148,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140441148,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1204994272","clinical_significance":[],"start":140441154,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","T"],"end":140441154,"strand":1,"feature_type":"variation"},{"alleles":["AA","AAA"],"end":140441155,"strand":1,"feature_type":"variation","start":140441154,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799833262","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441159,"source":"dbSNP","strand":1,"feature_type":"variation","end":140441159,"alleles":["G","A"],"seq_region_name":"7","id":"rs1799833295","clinical_significance":[]},{"end":140441171,"alleles":["ACTTTGGGAGA","-"],"strand":1,"feature_type":"variation","start":140441161,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799833323","clinical_significance":[]},{"id":"rs1799833351","seq_region_name":"7","clinical_significance":[],"start":140441162,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140441162,"strand":1,"feature_type":"variation"},{"alleles":["T","C"],"end":140441164,"feature_type":"variation","strand":1,"source":"dbSNP","start":140441164,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs62490428","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1563080669","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140441165,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441165,"source":"dbSNP"},{"start":140441170,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","C"],"end":140441170,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130203452","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799833431","source":"dbSNP","start":140441171,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140441171,"feature_type":"variation","strand":1},{"alleles":["C","G"],"end":140441173,"feature_type":"variation","strand":1,"source":"dbSNP","start":140441173,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1309130804"},{"clinical_significance":[],"seq_region_name":"7","id":"rs62490429","source":"dbSNP","start":140441174,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140441174,"alleles":["A","G"],"feature_type":"variation","strand":1},{"id":"rs746844780","seq_region_name":"7","clinical_significance":[],"start":140441175,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140441175,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"alleles":["G","A"],"end":140441176,"strand":1,"feature_type":"variation","start":140441176,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs555327127","clinical_significance":[]},{"seq_region_name":"7","id":"rs138424618","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441178,"source":"dbSNP","strand":1,"feature_type":"variation","end":140441178,"alleles":["C","T"]},{"alleles":["G","A","T"],"end":140441179,"feature_type":"variation","strand":1,"source":"dbSNP","start":140441179,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs540835713","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140441180,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441180,"clinical_significance":[],"id":"rs1355069301","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1308976550","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441182,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140441182},{"seq_region_name":"7","id":"rs1799834075","clinical_significance":[],"start":140441184,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140441184,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799834098","end":140441205,"alleles":["CTGAGGTCAGGAGTTC","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140441190,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140441193,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441193,"clinical_significance":[],"seq_region_name":"7","id":"rs1799834123"},{"id":"rs1799834142","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441199,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140441199},{"start":140441200,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A","C"],"end":140441200,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs559970496","clinical_significance":[]},{"seq_region_name":"7","id":"rs553167736","clinical_significance":[],"start":140441202,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A","C"],"end":140441202,"strand":1,"feature_type":"variation"},{"id":"rs1799834242","seq_region_name":"7","clinical_significance":[],"start":140441205,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140441205,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs577711212","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140441206,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441206},{"start":140441208,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140441208,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130203552","clinical_significance":[]},{"end":140441209,"alleles":["A","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140441209,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1463874269"},{"clinical_significance":[],"id":"rs1799834318","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441212,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140441212},{"clinical_significance":[],"seq_region_name":"7","id":"rs1249680869","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441217,"feature_type":"variation","strand":1,"end":140441217,"alleles":["G","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1170353413","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441219,"feature_type":"variation","strand":1,"end":140441219,"alleles":["C","G","T"]},{"end":140441222,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140441222,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799834396","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799834419","feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140441223,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441223},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441225,"source":"dbSNP","strand":1,"feature_type":"variation","end":140441225,"alleles":["T","C"],"id":"rs1799834451","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1406519307","seq_region_name":"7","source":"dbSNP","start":140441228,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140441228,"feature_type":"variation","strand":1},{"id":"rs1799834483","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["AAA","AAAA"],"end":140441232,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441230,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140441231,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441231,"clinical_significance":[],"seq_region_name":"7","id":"rs1799834507"},{"seq_region_name":"7","id":"rs1463424514","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441232,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140441232},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441233,"feature_type":"variation","strand":1,"end":140441236,"alleles":["CCCC","CCCCC"],"clinical_significance":[],"id":"rs1799834562","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1189450091","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441235,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140441235},{"clinical_significance":[],"seq_region_name":"7","id":"rs1192195706","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441236,"feature_type":"variation","strand":1,"end":140441236,"alleles":["C","A","G","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs545138322","feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140441237,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441237},{"source":"dbSNP","start":140441241,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140441241,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1478467151"},{"alleles":["T","C"],"end":140441242,"strand":1,"feature_type":"variation","start":140441242,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs965226298","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140441246,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441246,"clinical_significance":[],"seq_region_name":"7","id":"rs1427205903"},{"clinical_significance":[],"id":"rs997532406","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441249,"feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140441249},{"clinical_significance":[],"id":"rs1203722414","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140441255,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441255},{"source":"dbSNP","start":140441257,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140441257,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1335409377"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140441260,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441260,"source":"dbSNP","seq_region_name":"7","id":"rs1029439693","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799834825","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140441261,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441261},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441262,"feature_type":"variation","strand":1,"end":140441262,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799834851"},{"strand":1,"feature_type":"variation","end":140441264,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441264,"source":"dbSNP","seq_region_name":"7","id":"rs1275060815","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs919116048","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441265,"feature_type":"variation","strand":1,"end":140441265,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1799834937","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140441266,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441266,"source":"dbSNP"},{"source":"dbSNP","start":140441267,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140441267,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs953399693"},{"clinical_significance":[],"seq_region_name":"7","id":"rs929149889","end":140441268,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140441268,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs190125858","clinical_significance":[],"strand":1,"feature_type":"variation","end":140441269,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441269,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1297978267","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441272,"source":"dbSNP","strand":1,"feature_type":"variation","end":140441272,"alleles":["G","A"]},{"source":"dbSNP","start":140441273,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140441273,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1442193562","seq_region_name":"7"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441274,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140441274,"clinical_significance":[],"id":"rs1397360059","seq_region_name":"7"},{"id":"rs1166402809","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441280,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140441280},{"source":"dbSNP","start":140441281,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140441281,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799835107"},{"id":"rs2130203744","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140441292,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441292,"source":"dbSNP"},{"source":"dbSNP","start":140441298,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140441298,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1391460064"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441300,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140441300,"id":"rs1459391320","seq_region_name":"7","clinical_significance":[]},{"id":"rs914646070","seq_region_name":"7","clinical_significance":[],"alleles":["G","A","C"],"end":140441301,"strand":1,"feature_type":"variation","start":140441301,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"id":"rs1159368740","seq_region_name":"7","clinical_significance":[],"start":140441305,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140441305,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1420570073","clinical_significance":[],"start":140441306,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140441306,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs2130203781","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140441309,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441309,"source":"dbSNP"},{"seq_region_name":"7","id":"rs967551078","clinical_significance":[],"start":140441311,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140441311,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441312,"source":"dbSNP","strand":1,"feature_type":"variation","end":140441312,"alleles":["G","A"],"id":"rs1799835269","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs530764490","clinical_significance":[],"strand":1,"feature_type":"variation","end":140441313,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441313,"source":"dbSNP"},{"start":140441316,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140441316,"alleles":["G","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799835330","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441318,"feature_type":"variation","strand":1,"end":140441318,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs943363704"},{"seq_region_name":"7","id":"rs1799835382","clinical_significance":[],"end":140441320,"alleles":["A","C","T"],"strand":1,"feature_type":"variation","start":140441320,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"end":140441322,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140441322,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs866979239"},{"alleles":["G","A"],"end":140441323,"strand":1,"feature_type":"variation","start":140441323,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1254841207","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799835469","source":"dbSNP","start":140441325,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140441325,"alleles":["T","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs543026447","clinical_significance":[],"start":140441332,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140441332,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"alleles":["G","A"],"end":140441333,"feature_type":"variation","strand":1,"source":"dbSNP","start":140441333,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799835518"},{"source":"dbSNP","start":140441334,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140441334,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs182867856"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441335,"source":"dbSNP","strand":1,"feature_type":"variation","end":140441335,"alleles":["G","A"],"seq_region_name":"7","id":"rs1272579722","clinical_significance":[]},{"id":"rs1799835601","seq_region_name":"7","clinical_significance":[],"start":140441343,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140441343,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140441344,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441344,"source":"dbSNP","id":"rs1261445888","seq_region_name":"7","clinical_significance":[]},{"end":140441345,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140441345,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1585448584","clinical_significance":[]},{"end":140441347,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140441347,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799835659","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799835678","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441349,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140441349},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799835702","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140441352,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441352},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441356,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140441356,"clinical_significance":[],"seq_region_name":"7","id":"rs1228461347"},{"alleles":["G","A"],"end":140441357,"strand":1,"feature_type":"variation","start":140441357,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"TF_binding_site_variant","seq_region_name":"7","id":"rs1252247855","clinical_significance":[]},{"consequence_type":"TF_binding_site_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441360,"feature_type":"variation","strand":1,"end":140441360,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1270013100"},{"seq_region_name":"7","id":"rs1799835829","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"TF_binding_site_variant","start":140441366,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140441366},{"clinical_significance":[],"seq_region_name":"7","id":"rs1010961866","consequence_type":"TF_binding_site_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441367,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140441367},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799835882","end":140441368,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140441368,"consequence_type":"TF_binding_site_variant","assembly_name":"GRCh38"},{"end":140441369,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140441369,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"TF_binding_site_variant","id":"rs1204385573","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140441370,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441370,"clinical_significance":[],"id":"rs1373706671","seq_region_name":"7"},{"seq_region_name":"7","id":"rs903218231","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441375,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140441375},{"end":140441375,"alleles":["T","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140441375,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799835977"},{"id":"rs1324427441","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441377,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140441377},{"clinical_significance":[],"seq_region_name":"7","id":"rs1440900930","end":140441379,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140441379,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1585448603","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441382,"feature_type":"variation","strand":1,"end":140441382,"alleles":["T","G"]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441383,"feature_type":"variation","strand":1,"end":140441385,"alleles":["GGG","GG"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799836076"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441387,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140441387,"seq_region_name":"7","id":"rs1799836096","clinical_significance":[]},{"start":140441391,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140441391,"alleles":["G","C"],"strand":1,"feature_type":"variation","id":"rs1799836119","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799836137","source":"dbSNP","start":140441392,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140441392,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140441393,"alleles":["G","C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441393,"clinical_significance":[],"id":"rs1799836164","seq_region_name":"7"},{"id":"rs1799836181","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140441394,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441394,"source":"dbSNP"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441395,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140441395,"clinical_significance":[],"seq_region_name":"7","id":"rs2130203977"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441398,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140441398,"clinical_significance":[],"seq_region_name":"7","id":"rs1563080727"},{"alleles":["CTCT","CT"],"end":140441402,"strand":1,"feature_type":"variation","start":140441399,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1563080728","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441400,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140441400,"clinical_significance":[],"id":"rs1389375788","seq_region_name":"7"},{"end":140441402,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","start":140441402,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1290268268","seq_region_name":"7","clinical_significance":[]},{"end":140441403,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140441403,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1288959667","clinical_significance":[]},{"id":"rs1799836326","seq_region_name":"7","clinical_significance":[],"end":140441407,"alleles":["TCTC","TC"],"strand":1,"feature_type":"variation","start":140441404,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140441405,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441405,"clinical_significance":[],"seq_region_name":"7","id":"rs1452409177"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441406,"source":"dbSNP","strand":1,"feature_type":"variation","end":140441405,"alleles":["-","AAAAA"],"seq_region_name":"7","id":"rs1799836372","clinical_significance":[]},{"source":"dbSNP","start":140441406,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140441406,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1454963988"},{"source":"dbSNP","start":140441406,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140441406,"alleles":["T","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799836412"},{"strand":1,"feature_type":"variation","end":140441406,"alleles":["-","A","AA","AAA","AAAAA","AAAAAA"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441407,"source":"dbSNP","seq_region_name":"7","id":"rs1799836443","clinical_significance":[]},{"seq_region_name":"7","id":"rs934614283","clinical_significance":[],"alleles":["C","A"],"end":140441407,"strand":1,"feature_type":"variation","start":140441407,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799836508","feature_type":"variation","strand":1,"alleles":["C","-"],"end":140441407,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441407},{"strand":1,"feature_type":"variation","end":140441427,"alleles":["AAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAA","AAAAAAAAAAAA","AAAAAAAAAAAAA","AAAAAAAAAAAAAA","AAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAA"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441408,"source":"dbSNP","id":"rs532595152","seq_region_name":"7","clinical_significance":[]},{"end":140441410,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140441410,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799836721","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1327538592","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441418,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140441418},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799836803","source":"dbSNP","start":140441418,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["AAAA","AAAAGAAAA"],"end":140441421,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799836821","end":140441423,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140441423,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1295632131","source":"dbSNP","start":140441424,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140441424,"alleles":["A","T"],"feature_type":"variation","strand":1},{"id":"rs1799836861","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441424,"source":"dbSNP","strand":1,"feature_type":"variation","end":140441426,"alleles":["AAA","AAATAAA"]},{"strand":1,"feature_type":"variation","alleles":["-","T"],"end":140441424,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441425,"source":"dbSNP","seq_region_name":"7","id":"rs1799836889","clinical_significance":[]},{"alleles":["A","C"],"end":140441426,"feature_type":"variation","strand":1,"source":"dbSNP","start":140441426,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs938966364"},{"end":140441427,"alleles":["A","C","T"],"strand":1,"feature_type":"variation","start":140441427,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1382206020","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799836937","end":140441427,"alleles":["-","AAAAT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140441428,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441428,"source":"dbSNP","strand":1,"feature_type":"variation","end":140441428,"alleles":["T","A"],"seq_region_name":"7","id":"rs1267021618","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799836990","feature_type":"variation","strand":1,"alleles":["TT","T"],"end":140441429,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441428},{"seq_region_name":"7","id":"rs1799837015","clinical_significance":[],"strand":1,"feature_type":"variation","end":140441431,"alleles":["TTAC","-"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441428,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1799837038","seq_region_name":"7","alleles":["TTACAC","-"],"end":140441433,"feature_type":"variation","strand":1,"source":"dbSNP","start":140441428,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140441431,"alleles":["C","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441431,"clinical_significance":[],"seq_region_name":"7","id":"rs1799837059"},{"clinical_significance":[],"id":"rs1297170361","seq_region_name":"7","source":"dbSNP","start":140441432,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140441432,"feature_type":"variation","strand":1},{"start":140441433,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","A","G"],"end":140441433,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1480188866","clinical_significance":[]},{"end":140441438,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140441438,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1585448659","clinical_significance":[]},{"end":140441440,"alleles":["AA","A"],"strand":1,"feature_type":"variation","start":140441439,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1435022141","clinical_significance":[]},{"start":140441445,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140441445,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799837179","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130204165","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441447,"feature_type":"variation","strand":1,"end":140441447,"alleles":["C","A"]},{"end":140441452,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140441452,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1377037242","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441461,"feature_type":"variation","strand":1,"alleles":["C","A","G","T"],"end":140441461,"clinical_significance":[],"seq_region_name":"7","id":"rs1799837227"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441462,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140441462,"clinical_significance":[],"id":"rs1799837252","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140441465,"alleles":["T","A","C","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441465,"source":"dbSNP","seq_region_name":"7","id":"rs1171528904","clinical_significance":[]},{"seq_region_name":"7","id":"rs1182944610","clinical_significance":[],"strand":1,"feature_type":"variation","end":140441476,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441476,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1799837300","seq_region_name":"7","source":"dbSNP","start":140441479,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140441479,"alleles":["C","A"],"feature_type":"variation","strand":1},{"id":"rs1799837332","seq_region_name":"7","clinical_significance":[],"start":140441481,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140441481,"strand":1,"feature_type":"variation"},{"start":140441483,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140441483,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs117325168","clinical_significance":[]},{"id":"rs1373595136","seq_region_name":"7","clinical_significance":[],"start":140441489,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140441489,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1195297075","source":"dbSNP","start":140441494,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140441494,"alleles":["C","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs149277297","alleles":["A","T"],"end":140441498,"feature_type":"variation","strand":1,"source":"dbSNP","start":140441498,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"start":140441499,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140441499,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1158381157","clinical_significance":[]},{"clinical_significance":[],"id":"rs1391827499","seq_region_name":"7","end":140441500,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140441500,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"end":140441521,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140441521,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs752837335","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441523,"feature_type":"variation","strand":1,"end":140441523,"alleles":["A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799837532"},{"start":140441524,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","C"],"end":140441524,"strand":1,"feature_type":"variation","id":"rs1799837557","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs757214495","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441526,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140441526},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441528,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140441528,"seq_region_name":"7","id":"rs959622762","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799837627","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140441532,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441532},{"alleles":["T","G"],"end":140441538,"strand":1,"feature_type":"variation","start":140441538,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs571918273","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs991135953","source":"dbSNP","start":140441541,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140441541,"alleles":["T","C"],"feature_type":"variation","strand":1},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441548,"feature_type":"variation","strand":1,"end":140441548,"alleles":["C","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1170631729"},{"seq_region_name":"7","id":"rs188813515","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441553,"source":"dbSNP","strand":1,"feature_type":"variation","end":140441553,"alleles":["A","C"]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441555,"source":"dbSNP","strand":1,"feature_type":"variation","end":140441555,"alleles":["C","G","T"],"id":"rs79110648","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs886837913","end":140441556,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140441556,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"alleles":["G","A","T"],"end":140441558,"strand":1,"feature_type":"variation","start":140441558,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs866457996","clinical_significance":[]},{"alleles":["T","C"],"end":140441564,"feature_type":"variation","strand":1,"source":"dbSNP","start":140441564,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1004006048"},{"end":140441566,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140441566,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799837882"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441567,"feature_type":"variation","strand":1,"alleles":["GGG","GG"],"end":140441569,"clinical_significance":[],"seq_region_name":"7","id":"rs1799837917"},{"clinical_significance":[],"seq_region_name":"7","id":"rs745842233","feature_type":"variation","strand":1,"end":140441569,"alleles":["G","C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441569},{"seq_region_name":"7","id":"rs1585448724","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441573,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140441573},{"start":140441574,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140441574,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs963004882","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441580,"source":"dbSNP","strand":1,"feature_type":"variation","end":140441580,"alleles":["A","G"],"seq_region_name":"7","id":"rs973163726","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs900996675","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140441584,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441584},{"start":140441585,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140441585,"alleles":["A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1277085215","clinical_significance":[]},{"start":140441588,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","G"],"end":140441588,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs997204843","clinical_significance":[]},{"source":"dbSNP","start":140441589,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140441589,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799838120"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441591,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140441591,"clinical_significance":[],"seq_region_name":"7","id":"rs1799838141"},{"clinical_significance":[],"seq_region_name":"7","id":"rs569771891","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441593,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140441593},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441594,"feature_type":"variation","strand":1,"alleles":["ACCAACAAGTTACAC","AC"],"end":140441608,"clinical_significance":[],"seq_region_name":"7","id":"rs1414945558"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441599,"source":"dbSNP","strand":1,"feature_type":"variation","end":140441599,"alleles":["C","T"],"id":"rs918993363","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799838245","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441604,"source":"dbSNP","strand":1,"feature_type":"variation","end":140441604,"alleles":["T","A","C"]},{"seq_region_name":"7","id":"rs1310795989","clinical_significance":[],"start":140441612,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140441616,"alleles":["AGGAG","AG"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140441613,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441613,"clinical_significance":[],"id":"rs1028223819","seq_region_name":"7"},{"id":"rs1396992303","seq_region_name":"7","clinical_significance":[],"start":140441614,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140441614,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs953532051","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441622,"feature_type":"variation","strand":1,"end":140441622,"alleles":["G","C"]},{"seq_region_name":"7","id":"rs878975447","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441623,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140441623},{"clinical_significance":[],"id":"rs1799838399","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140441627,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441627},{"id":"rs987292719","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441629,"source":"dbSNP","strand":1,"feature_type":"variation","end":140441629,"alleles":["T","C"]},{"id":"rs911816295","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441630,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140441630},{"source":"dbSNP","start":140441638,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140441638,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130204446"},{"feature_type":"variation","strand":1,"end":140441639,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441639,"clinical_significance":[],"seq_region_name":"7","id":"rs1238158185"},{"end":140441640,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140441640,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs758249005","seq_region_name":"7","clinical_significance":[]},{"id":"rs1039061500","seq_region_name":"7","clinical_significance":[],"end":140441642,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140441642,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"end":140441643,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140441643,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1021735629","seq_region_name":"7"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441645,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140441645,"clinical_significance":[],"seq_region_name":"7","id":"rs1799838596"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799838611","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441646,"feature_type":"variation","strand":1,"end":140441646,"alleles":["T","C"]},{"id":"rs967423167","seq_region_name":"7","clinical_significance":[],"start":140441652,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140441652,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140441653,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441653,"source":"dbSNP","seq_region_name":"7","id":"rs893846330","clinical_significance":[]},{"source":"dbSNP","start":140441655,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140441655,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs946697286"},{"seq_region_name":"7","id":"rs1207838539","clinical_significance":[],"strand":1,"feature_type":"variation","end":140441657,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441657,"source":"dbSNP"},{"alleles":["T","C"],"end":140441664,"strand":1,"feature_type":"variation","start":140441664,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs796121152","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799838759","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140441666,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441666,"source":"dbSNP"},{"id":"rs1799838779","seq_region_name":"7","clinical_significance":[],"start":140441669,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140441669,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140441678,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441678,"clinical_significance":[],"id":"rs2130204513","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441679,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140441679,"id":"rs1256824017","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799838825","source":"dbSNP","start":140441681,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140441681,"feature_type":"variation","strand":1},{"end":140441682,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140441682,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs902584808"},{"id":"rs1799838880","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140441686,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441686,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799838899","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140441694,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441694,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799838930","clinical_significance":[],"end":140441695,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140441695,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"source":"dbSNP","start":140441696,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140441696,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1336373653"},{"seq_region_name":"7","id":"rs1446917535","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441697,"source":"dbSNP","strand":1,"feature_type":"variation","end":140441697,"alleles":["A","C"]},{"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140441702,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441702,"source":"dbSNP","id":"rs2130204563","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140441708,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441708,"clinical_significance":[],"seq_region_name":"7","id":"rs977496229"},{"clinical_significance":[],"seq_region_name":"7","id":"rs780057689","end":140441712,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140441712,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs536614931","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441714,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140441714},{"seq_region_name":"7","id":"rs1799839071","clinical_significance":[],"start":140441716,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140441716,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1330650506","clinical_significance":[],"start":140441718,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140441718,"strand":1,"feature_type":"variation"},{"end":140441720,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140441720,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs527515548","clinical_significance":[]},{"start":140441723,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140441723,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799839161","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140441726,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441726,"source":"dbSNP","seq_region_name":"7","id":"rs1799839190","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799839212","seq_region_name":"7","source":"dbSNP","start":140441736,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140441736,"alleles":["A","-"],"feature_type":"variation","strand":1},{"end":140441737,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140441737,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1035173198","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799839284","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441739,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140441739},{"alleles":["TT","-"],"end":140441743,"strand":1,"feature_type":"variation","start":140441742,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799839307","clinical_significance":[]},{"clinical_significance":[],"id":"rs746639930","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441743,"feature_type":"variation","strand":1,"end":140441743,"alleles":["T","C"]},{"start":140441755,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","T"],"end":140441755,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs895407761","clinical_significance":[]},{"start":140441757,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140441757,"strand":1,"feature_type":"variation","id":"rs1799839356","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799839377","seq_region_name":"7","alleles":["A","C"],"end":140441759,"feature_type":"variation","strand":1,"source":"dbSNP","start":140441759,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"end":140441768,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140441768,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130204646"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130204648","alleles":["A","G"],"end":140441776,"feature_type":"variation","strand":1,"source":"dbSNP","start":140441776,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1799839416","clinical_significance":[],"strand":1,"feature_type":"variation","end":140441777,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441777,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1012421199","feature_type":"variation","strand":1,"end":140441784,"alleles":["A","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441784},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799839491","alleles":["C","G"],"end":140441785,"feature_type":"variation","strand":1,"source":"dbSNP","start":140441785,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs768362658","source":"dbSNP","start":140441786,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140441786,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1563080825","clinical_significance":[],"end":140441790,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140441790,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs992182810","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140441792,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441792,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1799839644","seq_region_name":"7","feature_type":"variation","strand":1,"end":140441797,"alleles":["T","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441797},{"end":140441799,"alleles":["GG","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140441798,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1254018639"},{"clinical_significance":[],"seq_region_name":"7","id":"rs555358844","alleles":["G","A"],"end":140441804,"feature_type":"variation","strand":1,"source":"dbSNP","start":140441804,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140441807,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441807,"clinical_significance":[],"id":"rs549164735","seq_region_name":"7"},{"id":"rs1799839778","seq_region_name":"7","clinical_significance":[],"start":140441808,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140441808,"strand":1,"feature_type":"variation"},{"id":"rs1740606783","seq_region_name":"7","clinical_significance":[],"end":140441812,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140441812,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"source":"dbSNP","start":140441813,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140441813,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs963035617"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140441820,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441820,"source":"dbSNP","seq_region_name":"7","id":"rs1417862041","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140441824,"alleles":["C","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441824,"clinical_significance":[],"id":"rs567433815","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs973078171","feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140441833,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441833},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799839971","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140441834,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441834},{"id":"rs1181651108","seq_region_name":"7","clinical_significance":[],"start":140441835,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140441835,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441842,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140441842,"clinical_significance":[],"id":"rs1180145190","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1792589293","source":"dbSNP","start":140441845,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140441845,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140441856,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441856,"clinical_significance":[],"seq_region_name":"7","id":"rs1799840068"},{"feature_type":"variation","strand":1,"end":140441861,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441861,"clinical_significance":[],"seq_region_name":"7","id":"rs1369541601"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799840126","end":140441862,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140441862,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1799840163","seq_region_name":"7","source":"dbSNP","start":140441865,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140441865,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1026494646","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441868,"feature_type":"variation","strand":1,"alleles":["TTTTTTT","TTTTTT"],"end":140441874},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441874,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140441874,"id":"rs531775899","seq_region_name":"7","clinical_significance":[]},{"end":140441875,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140441875,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs950472346","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs367608100","clinical_significance":[],"end":140441876,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140441876,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1474019171","clinical_significance":[],"end":140441877,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140441877,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"start":140441880,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140441880,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs1162022654","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799840410","clinical_significance":[],"start":140441884,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140441884,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"end":140441885,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140441885,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1048013262","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799840452","clinical_significance":[],"start":140441890,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140441890,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140441893,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441893,"clinical_significance":[],"seq_region_name":"7","id":"rs1799840473"},{"id":"rs775942893","seq_region_name":"7","clinical_significance":[],"start":140441897,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140441897,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140441904,"alleles":["A","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441904,"clinical_significance":[],"id":"rs2130204847","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441904,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AAGTA","AAGTATGATATGTAAGTAAATAAGTA"],"end":140441908,"seq_region_name":"7","id":"rs1799840524","clinical_significance":[]},{"alleles":["G","A"],"end":140441906,"strand":1,"feature_type":"variation","start":140441906,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1384278654","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799840583","clinical_significance":[],"alleles":["A","C"],"end":140441909,"strand":1,"feature_type":"variation","start":140441909,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"id":"rs147392733","seq_region_name":"7","source":"dbSNP","start":140441914,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140441914,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1227325170","clinical_significance":[],"alleles":["T","C"],"end":140441916,"strand":1,"feature_type":"variation","start":140441916,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799840661","source":"dbSNP","start":140441927,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140441927,"alleles":["G","C"],"feature_type":"variation","strand":1},{"alleles":["G","A"],"end":140441930,"strand":1,"feature_type":"variation","start":140441930,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs568687269","clinical_significance":[]},{"alleles":["A","G"],"end":140441934,"feature_type":"variation","strand":1,"source":"dbSNP","start":140441934,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1350946754"},{"id":"rs1281034677","seq_region_name":"7","clinical_significance":[],"start":140441936,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140441936,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"start":140441937,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","G"],"end":140441937,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs747713596","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799840750","alleles":["T","C"],"end":140441939,"feature_type":"variation","strand":1,"source":"dbSNP","start":140441939,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"start":140441948,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140441948,"strand":1,"feature_type":"variation","id":"rs1799840768","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs939805987","feature_type":"variation","strand":1,"end":140441949,"alleles":["C","A","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441949},{"seq_region_name":"7","id":"rs1040767188","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140441950,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441950,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs911694288","end":140441951,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140441951,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1799840884","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441952,"source":"dbSNP","strand":1,"feature_type":"variation","end":140441952,"alleles":["C","T"]},{"clinical_significance":[],"id":"rs1799840910","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140441954,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441954},{"end":140441955,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140441955,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs943175822","clinical_significance":[]},{"seq_region_name":"7","id":"rs1443099101","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["CACA","CACACA"],"end":140441962,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441959,"source":"dbSNP"},{"id":"rs1799840985","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441960,"source":"dbSNP","strand":1,"feature_type":"variation","end":140441965,"alleles":["ACAACA","ACA"]},{"start":140441964,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140441964,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799841015","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799841036","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441972,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140441972},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441974,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140441974,"clinical_significance":[],"id":"rs139675846","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs932488466","alleles":["G","A"],"end":140441978,"feature_type":"variation","strand":1,"source":"dbSNP","start":140441978,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"start":140441980,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","C"],"end":140441980,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs915145208","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1050120954","feature_type":"variation","strand":1,"end":140441981,"alleles":["G","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441981},{"source":"dbSNP","start":140441988,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140441988,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130205007"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441990,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140441990,"seq_region_name":"7","id":"rs1799841185","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140441993,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441993,"clinical_significance":[],"seq_region_name":"7","id":"rs893700118"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1011586194","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140441994,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140441994},{"seq_region_name":"7","id":"rs1799841252","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441995,"source":"dbSNP","strand":1,"feature_type":"variation","end":140441995,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs544806613","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140441996,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140441996,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1799841304","seq_region_name":"7","source":"dbSNP","start":140441998,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140441998,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1157096027","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140442002,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442002},{"seq_region_name":"7","id":"rs567589423","clinical_significance":[],"strand":1,"feature_type":"variation","end":140442004,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442004,"source":"dbSNP"},{"start":140442010,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140442010,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","id":"rs924041382","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799841412","end":140442012,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140442012,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140442013,"alleles":["A","-"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442013,"clinical_significance":[],"id":"rs1799841430","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1196033138","clinical_significance":[],"strand":1,"feature_type":"variation","end":140442014,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442014,"source":"dbSNP"},{"seq_region_name":"7","id":"rs903183513","clinical_significance":[],"end":140442015,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140442015,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799841489","feature_type":"variation","strand":1,"end":140442016,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442016},{"id":"rs2130205093","seq_region_name":"7","clinical_significance":[],"alleles":["G","C"],"end":140442017,"strand":1,"feature_type":"variation","start":140442017,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"start":140442018,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","G"],"end":140442018,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799841507","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442020,"feature_type":"variation","strand":1,"end":140442020,"alleles":["T","C"],"clinical_significance":[],"id":"rs575705468","seq_region_name":"7"},{"alleles":["T","C"],"end":140442029,"strand":1,"feature_type":"variation","start":140442029,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs763499494","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799841616","end":140442031,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140442031,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1447170933","feature_type":"variation","strand":1,"end":140442037,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442037},{"seq_region_name":"7","id":"rs1799841663","clinical_significance":[],"strand":1,"feature_type":"variation","end":140442038,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442038,"source":"dbSNP"},{"id":"rs1799841686","seq_region_name":"7","clinical_significance":[],"alleles":["A","T"],"end":140442041,"strand":1,"feature_type":"variation","start":140442041,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1799841709","clinical_significance":[],"strand":1,"feature_type":"variation","end":140442045,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442045,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["ATAAAAAATTTAAAAATAAAAAATT","ATAAAAAATT"],"end":140442071,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442047,"source":"dbSNP","seq_region_name":"7","id":"rs889699399","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585448943","clinical_significance":[],"end":140442056,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140442056,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1799841788","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140442057,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442057,"source":"dbSNP"},{"seq_region_name":"7","id":"rs960499390","clinical_significance":[],"start":140442063,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140442063,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585448952","alleles":["AAAAAA","AAAAA"],"end":140442069,"feature_type":"variation","strand":1,"source":"dbSNP","start":140442064,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799841854","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442069,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140442069},{"seq_region_name":"7","id":"rs991650163","clinical_significance":[],"start":140442075,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140442075,"strand":1,"feature_type":"variation"},{"end":140442076,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140442076,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs776521186"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1276884238","source":"dbSNP","start":140442078,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140442078,"feature_type":"variation","strand":1},{"start":140442081,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140442081,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799841962","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563080879","alleles":["G","C"],"end":140442086,"feature_type":"variation","strand":1,"source":"dbSNP","start":140442086,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1799841990","clinical_significance":[],"end":140442088,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140442088,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1479733957","source":"dbSNP","start":140442091,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140442091,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1799842043","seq_region_name":"7","source":"dbSNP","start":140442097,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140442097,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442103,"source":"dbSNP","strand":1,"feature_type":"variation","end":140442103,"alleles":["C","T"],"seq_region_name":"7","id":"rs1799842062","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799842084","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140442107,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442107},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130205213","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442110,"feature_type":"variation","strand":1,"end":140442110,"alleles":["T","C"]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442111,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140442111,"seq_region_name":"7","id":"rs1799842100","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442113,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140442113,"clinical_significance":[],"seq_region_name":"7","id":"rs1799842124"},{"alleles":["G","A"],"end":140442114,"feature_type":"variation","strand":1,"source":"dbSNP","start":140442114,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799842142"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130205223","source":"dbSNP","start":140442115,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140442115,"alleles":["G","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs193064786","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442117,"feature_type":"variation","strand":1,"alleles":["G","A","C","T"],"end":140442117},{"alleles":["GGGGGGG","GGGGGG","GGGGGGGG"],"end":140442123,"strand":1,"feature_type":"variation","start":140442117,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1236332779","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs984327821","source":"dbSNP","start":140442118,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A","C","T"],"end":140442118,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1316489028","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442118,"source":"dbSNP","strand":1,"feature_type":"variation","end":140442126,"alleles":["GGGGGGAAG","G"]},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140442119,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442119,"clinical_significance":[],"seq_region_name":"7","id":"rs1799842311"},{"end":140442121,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140442121,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs908253716","clinical_significance":[]},{"start":140442123,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A","T"],"end":140442123,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1257535008","clinical_significance":[]},{"source":"dbSNP","start":140442125,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140442125,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1444613813"},{"alleles":["A","G"],"end":140442130,"feature_type":"variation","strand":1,"source":"dbSNP","start":140442130,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs6963738"},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140442132,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442132,"clinical_significance":[],"seq_region_name":"7","id":"rs1799842516"},{"end":140442133,"alleles":["GG","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140442132,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799842548"},{"source":"dbSNP","start":140442133,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140442133,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1425114947","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442134,"source":"dbSNP","strand":1,"feature_type":"variation","end":140442134,"alleles":["C","G"],"id":"rs1799842595","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442144,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140442144,"seq_region_name":"7","id":"rs1187670313","clinical_significance":[]},{"alleles":["A","C","G"],"end":140442147,"strand":1,"feature_type":"variation","start":140442147,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1384961803","clinical_significance":[]},{"alleles":["G","C"],"end":140442149,"feature_type":"variation","strand":1,"source":"dbSNP","start":140442149,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799842674"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442151,"feature_type":"variation","strand":1,"end":140442151,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799842710"},{"id":"rs1799842735","seq_region_name":"7","clinical_significance":[],"end":140442153,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140442153,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"strand":1,"feature_type":"variation","end":140442154,"alleles":["C","A","G","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442154,"source":"dbSNP","id":"rs1243416110","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1449709983","alleles":["G","A"],"end":140442155,"feature_type":"variation","strand":1,"source":"dbSNP","start":140442155,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"start":140442166,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140442166,"strand":1,"feature_type":"variation","id":"rs1487766045","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1212796511","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442173,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140442173},{"end":140442178,"alleles":["GATCGA","GA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140442173,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1280697965"},{"seq_region_name":"7","id":"rs1310268669","clinical_significance":[],"strand":1,"feature_type":"variation","end":140442175,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442175,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1277789512","feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140442176,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442176},{"id":"rs1170153491","seq_region_name":"7","clinical_significance":[],"start":140442177,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140442177,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140442178,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442178,"clinical_significance":[],"seq_region_name":"7","id":"rs1370979811"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442179,"feature_type":"variation","strand":1,"end":140442179,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799842981"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442187,"source":"dbSNP","strand":1,"feature_type":"variation","end":140442187,"alleles":["A","G"],"id":"rs1364152562","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1268501675","seq_region_name":"7","source":"dbSNP","start":140442197,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140442197,"feature_type":"variation","strand":1},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442204,"feature_type":"variation","strand":1,"alleles":["A","-"],"end":140442204,"clinical_significance":[],"seq_region_name":"7","id":"rs1799843042"},{"alleles":["G","A"],"end":140442207,"strand":1,"feature_type":"variation","start":140442207,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1399557353","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1356369502","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442208,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140442208},{"clinical_significance":[],"id":"rs1315121846","seq_region_name":"7","feature_type":"variation","strand":1,"end":140442213,"alleles":["C","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442213},{"id":"rs1799843191","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442214,"source":"dbSNP","strand":1,"feature_type":"variation","end":140442214,"alleles":["C","G"]},{"seq_region_name":"7","id":"rs1799843217","clinical_significance":[],"start":140442215,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140442215,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs550484308","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442216,"feature_type":"variation","strand":1,"end":140442216,"alleles":["T","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1018704408","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442219,"feature_type":"variation","strand":1,"end":140442219,"alleles":["C","T"]},{"strand":1,"feature_type":"variation","alleles":["AAAAAAAA","AAAAAAAAA"],"end":140442229,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442222,"source":"dbSNP","seq_region_name":"7","id":"rs1404290489","clinical_significance":[]},{"start":140442225,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140442225,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs922347699","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["AAAGAAAGAA","AAAGAA"],"end":140442236,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442227,"source":"dbSNP","seq_region_name":"7","id":"rs1585449053","clinical_significance":[]},{"alleles":["A","C"],"end":140442228,"strand":1,"feature_type":"variation","start":140442228,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799843364","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140442229,"alleles":["A","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442229,"clinical_significance":[],"seq_region_name":"7","id":"rs932495335"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442230,"feature_type":"variation","strand":1,"end":140442230,"alleles":["G","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799843412"},{"source":"dbSNP","start":140442231,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140442231,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1049539473"},{"seq_region_name":"7","id":"rs1365590230","clinical_significance":[],"alleles":["A","G"],"end":140442233,"strand":1,"feature_type":"variation","start":140442233,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442234,"feature_type":"variation","strand":1,"alleles":["G","C","T"],"end":140442234,"clinical_significance":[],"id":"rs1436994781","seq_region_name":"7"},{"end":140442242,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140442242,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799843519","clinical_significance":[]},{"clinical_significance":[],"id":"rs974562040","seq_region_name":"7","source":"dbSNP","start":140442245,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140442245,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs572002104","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442250,"source":"dbSNP","strand":1,"feature_type":"variation","end":140442250,"alleles":["C","A","G","T"]},{"clinical_significance":[],"id":"rs1477269204","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442252,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140442252},{"id":"rs1799843624","seq_region_name":"7","clinical_significance":[],"start":140442253,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140442253,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"end":140442255,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140442255,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1226851362","clinical_significance":[]},{"clinical_significance":[],"id":"rs1189676983","seq_region_name":"7","source":"dbSNP","start":140442261,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140442261,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs946655982","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140442264,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442264},{"seq_region_name":"7","id":"rs1205057119","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140442265,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442265,"source":"dbSNP"},{"seq_region_name":"7","id":"rs978502112","clinical_significance":[],"end":140442266,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140442266,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1236742198","clinical_significance":[],"start":140442266,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140442271,"alleles":["TTTTTT","TTTTTTT"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442271,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140442271,"seq_region_name":"7","id":"rs1309186789","clinical_significance":[]},{"start":140442280,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140442280,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs923933240","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442281,"feature_type":"variation","strand":1,"end":140442281,"alleles":["A","C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1256615149"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1218113904","end":140442282,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140442282,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1799843857","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140442283,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442283},{"alleles":["T","A"],"end":140442286,"strand":1,"feature_type":"variation","start":140442286,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1042310887","clinical_significance":[]},{"end":140442291,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140442291,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799843909","clinical_significance":[]},{"id":"rs1585449086","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140442292,"strand":1,"feature_type":"variation","start":140442292,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"alleles":["TTTGTTT","TTT"],"end":140442299,"feature_type":"variation","strand":1,"source":"dbSNP","start":140442293,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs540480302"},{"clinical_significance":[],"seq_region_name":"7","id":"rs895881730","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442296,"feature_type":"variation","strand":1,"end":140442296,"alleles":["G","C","T"]},{"source":"dbSNP","start":140442301,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140442301,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1378889599"},{"seq_region_name":"7","id":"rs1799844021","clinical_significance":[],"strand":1,"feature_type":"variation","end":140442302,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442302,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140442303,"alleles":["A","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442303,"clinical_significance":[],"id":"rs1012763574","seq_region_name":"7"},{"source":"dbSNP","start":140442303,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140442304,"alleles":["AC","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs756022842"},{"clinical_significance":[],"id":"rs1585449103","seq_region_name":"7","end":140442304,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140442304,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799844114","source":"dbSNP","start":140442304,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","-"],"end":140442304,"feature_type":"variation","strand":1},{"end":140442305,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140442305,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1799844142","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442305,"feature_type":"variation","strand":1,"alleles":["TTTTTTTTTTTTTTTTTTT","TTTTTTTTTTT","TTTTTTTTTTTT","TTTTTTTTTTTTTT","TTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTT"],"end":140442323,"clinical_significance":[],"seq_region_name":"7","id":"rs1167859715"},{"clinical_significance":[],"id":"rs1799844304","seq_region_name":"7","end":140442307,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140442307,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442308,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140442308,"clinical_significance":[],"id":"rs1799844334","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1166629332","clinical_significance":[],"end":140442312,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140442312,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"feature_type":"variation","strand":1,"end":140442314,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442314,"clinical_significance":[],"seq_region_name":"7","id":"rs1799844388"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140442316,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442316,"source":"dbSNP","id":"rs1585449114","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140442323,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442323,"source":"dbSNP","seq_region_name":"7","id":"rs1799844434","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799844458","seq_region_name":"7","source":"dbSNP","start":140442323,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140442324,"alleles":["TG","-"],"feature_type":"variation","strand":1},{"end":140442324,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140442324,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1162995210","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1421701501","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442324,"feature_type":"variation","strand":1,"end":140442324,"alleles":["G","-"]},{"clinical_significance":[],"id":"rs1799844520","seq_region_name":"7","alleles":["GAGATGGAG","-"],"end":140442332,"feature_type":"variation","strand":1,"source":"dbSNP","start":140442324,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1190873163","feature_type":"variation","strand":1,"alleles":["A","T"],"end":140442325,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442325},{"source":"dbSNP","start":140442325,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140442325,"alleles":["A","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799844551","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs939342338","source":"dbSNP","start":140442326,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140442326,"alleles":["G","A","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1259292339","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442327,"source":"dbSNP","strand":1,"feature_type":"variation","end":140442327,"alleles":["A","T"]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442331,"feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140442331,"clinical_significance":[],"seq_region_name":"7","id":"rs1023248506"},{"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140442333,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442333,"clinical_significance":[],"id":"rs1585449132","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1427500694","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442334,"feature_type":"variation","strand":1,"end":140442334,"alleles":["C","A","T"]},{"feature_type":"variation","strand":1,"end":140442336,"alleles":["T","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442336,"clinical_significance":[],"id":"rs1799844672","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799844699","alleles":["G","A","T"],"end":140442337,"feature_type":"variation","strand":1,"source":"dbSNP","start":140442337,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140442341,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140442341,"alleles":["T","A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1056574497"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442342,"feature_type":"variation","strand":1,"end":140442342,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs898979539"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442346,"feature_type":"variation","strand":1,"end":140442346,"alleles":["C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs916648463"},{"seq_region_name":"7","id":"rs2130205744","clinical_significance":[],"start":140442347,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140442347,"strand":1,"feature_type":"variation"},{"id":"rs1799844829","seq_region_name":"7","clinical_significance":[],"start":140442351,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140442351,"strand":1,"feature_type":"variation"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442353,"feature_type":"variation","strand":1,"end":140442353,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1242808251"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1321355999","source":"dbSNP","start":140442359,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140442359,"feature_type":"variation","strand":1},{"start":140442362,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140442362,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs184155095","clinical_significance":[]},{"seq_region_name":"7","id":"rs1225858309","clinical_significance":[],"start":140442363,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A","C"],"end":140442363,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140442365,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442365,"source":"dbSNP","seq_region_name":"7","id":"rs998829676","clinical_significance":[]},{"alleles":["C","T"],"end":140442367,"strand":1,"feature_type":"variation","start":140442367,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1458658568","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A","C","T"],"end":140442368,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442368,"clinical_significance":[],"seq_region_name":"7","id":"rs898754046"},{"id":"rs1799844993","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140442371,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442371,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1036205026","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442374,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140442374},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585449160","feature_type":"variation","strand":1,"end":140442379,"alleles":["A","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442379},{"clinical_significance":[],"seq_region_name":"7","id":"rs1047753936","source":"dbSNP","start":140442381,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140442381,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1456021814","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442385,"feature_type":"variation","strand":1,"end":140442385,"alleles":["A","C","G"]},{"start":140442386,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140442386,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1348961416","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442387,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140442387,"seq_region_name":"7","id":"rs895862366","clinical_significance":[]},{"id":"rs1360162568","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442390,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140442390},{"clinical_significance":[],"id":"rs1013511119","seq_region_name":"7","source":"dbSNP","start":140442391,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140442391,"feature_type":"variation","strand":1},{"alleles":["C","G"],"end":140442393,"feature_type":"variation","strand":1,"source":"dbSNP","start":140442393,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1302079641"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140442397,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442397,"clinical_significance":[],"seq_region_name":"7","id":"rs886146232"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140442398,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442398,"clinical_significance":[],"seq_region_name":"7","id":"rs1177922401"},{"clinical_significance":[],"id":"rs1799845255","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140442399,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442399},{"clinical_significance":[],"id":"rs532708797","seq_region_name":"7","source":"dbSNP","start":140442400,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140442400,"feature_type":"variation","strand":1},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442401,"feature_type":"variation","strand":1,"end":140442401,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130205884"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442403,"feature_type":"variation","strand":1,"end":140442421,"alleles":["CAAGCGATTCTCCTGCCTC","CAAGCGATTCTCCTGCCTCCAAGCGATTCTCCTGCCTC"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799845311"},{"clinical_significance":[],"id":"rs1799845334","seq_region_name":"7","source":"dbSNP","start":140442404,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140442405,"alleles":["AA","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799845359","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442407,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140442407},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799845376","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140442408,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442408},{"seq_region_name":"7","id":"rs1254896696","clinical_significance":[],"alleles":["T","A","C"],"end":140442410,"strand":1,"feature_type":"variation","start":140442410,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140442420,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442420,"source":"dbSNP","seq_region_name":"7","id":"rs1221758393","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799845425","source":"dbSNP","start":140442423,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140442423,"alleles":["G","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs551218384","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140442429,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442429},{"id":"rs1208165982","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["-","A"],"end":140442429,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442430,"source":"dbSNP"},{"id":"rs569733415","seq_region_name":"7","clinical_significance":[],"end":140442430,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140442430,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"alleles":["A","G"],"end":140442431,"strand":1,"feature_type":"variation","start":140442431,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1218290969","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140442432,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442432,"clinical_significance":[],"id":"rs1799845603","seq_region_name":"7"},{"alleles":["T","C"],"end":140442437,"strand":1,"feature_type":"variation","start":140442437,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs376099374","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442439,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140442439,"seq_region_name":"7","id":"rs774844149","clinical_significance":[]},{"source":"dbSNP","start":140442442,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140442442,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1235572428"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442444,"source":"dbSNP","strand":1,"feature_type":"variation","end":140442444,"alleles":["G","C"],"seq_region_name":"7","id":"rs1799845717","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799845744","source":"dbSNP","start":140442446,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140442446,"feature_type":"variation","strand":1},{"alleles":["G","A","T"],"end":140442448,"feature_type":"variation","strand":1,"source":"dbSNP","start":140442448,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs759608797","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140442453,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442453,"source":"dbSNP","seq_region_name":"7","id":"rs2130205993","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442456,"feature_type":"variation","strand":1,"end":140442456,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799845800"},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140442458,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442458,"clinical_significance":[],"seq_region_name":"7","id":"rs548680764"},{"strand":1,"feature_type":"variation","end":140442461,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442461,"source":"dbSNP","id":"rs1015783025","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs567292848","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442462,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140442462},{"feature_type":"variation","strand":1,"end":140442465,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442465,"clinical_significance":[],"seq_region_name":"7","id":"rs765152872"},{"clinical_significance":[],"seq_region_name":"7","id":"rs774359157","source":"dbSNP","start":140442466,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140442466,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs534330279","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140442468,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442468},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130206035","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442473,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140442473},{"id":"rs546443289","seq_region_name":"7","clinical_significance":[],"alleles":["A","G"],"end":140442479,"strand":1,"feature_type":"variation","start":140442479,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"alleles":["T","C"],"end":140442480,"feature_type":"variation","strand":1,"source":"dbSNP","start":140442480,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1485341498"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1289085017","source":"dbSNP","start":140442481,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","A","C"],"end":140442481,"feature_type":"variation","strand":1},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442482,"feature_type":"variation","strand":1,"end":140442482,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585449217"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799846078","source":"dbSNP","start":140442485,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140442485,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442487,"source":"dbSNP","strand":1,"feature_type":"variation","end":140442487,"alleles":["T","C"],"seq_region_name":"7","id":"rs77170916","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140442493,"alleles":["T","A","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442493,"clinical_significance":[],"id":"rs75932296","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442494,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140442494,"id":"rs79201217","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs79790527","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442495,"source":"dbSNP","strand":1,"feature_type":"variation","end":140442495,"alleles":["G","A"]},{"source":"dbSNP","start":140442496,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140442496,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs78786315"},{"seq_region_name":"7","id":"rs74705759","clinical_significance":[],"start":140442497,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","C"],"end":140442497,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442501,"source":"dbSNP","strand":1,"feature_type":"variation","end":140442501,"alleles":["C","T"],"seq_region_name":"7","id":"rs976364319","clinical_significance":[]},{"alleles":["A","T"],"end":140442502,"strand":1,"feature_type":"variation","start":140442502,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1358332448","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799846276","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140442504,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442504,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs563158938","source":"dbSNP","start":140442506,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","TT"],"end":140442506,"feature_type":"variation","strand":1},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442506,"feature_type":"variation","strand":1,"end":140442506,"alleles":["T","C","G"],"clinical_significance":[],"id":"rs1435216889","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs76298154","feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140442507,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442507},{"seq_region_name":"7","id":"rs79729289","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442510,"source":"dbSNP","strand":1,"feature_type":"variation","end":140442510,"alleles":["G","A"]},{"strand":1,"feature_type":"variation","end":140442511,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442511,"source":"dbSNP","seq_region_name":"7","id":"rs1799846408","clinical_significance":[]},{"alleles":["G","C","T"],"end":140442515,"strand":1,"feature_type":"variation","start":140442515,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs77806283","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140442520,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442520,"clinical_significance":[],"seq_region_name":"7","id":"rs78790012"},{"clinical_significance":[],"id":"rs80248487","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140442524,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442524},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442525,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140442525,"seq_region_name":"7","id":"rs77296098","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442525,"feature_type":"variation","strand":1,"end":140442525,"alleles":["T","TT"],"clinical_significance":[],"seq_region_name":"7","id":"rs761410492"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799846549","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442529,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140442529},{"seq_region_name":"7","id":"rs1799846581","clinical_significance":[],"start":140442530,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","G"],"end":140442530,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1196733408","end":140442532,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140442532,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442534,"feature_type":"variation","strand":1,"end":140442534,"alleles":["A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1432664240"},{"source":"dbSNP","start":140442536,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140442536,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799846644"},{"seq_region_name":"7","id":"rs78460089","clinical_significance":[],"alleles":["C","G","T"],"end":140442538,"strand":1,"feature_type":"variation","start":140442538,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"alleles":["G","A","C"],"end":140442539,"feature_type":"variation","strand":1,"source":"dbSNP","start":140442539,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs761935686"},{"clinical_significance":[],"seq_region_name":"7","id":"rs978071403","feature_type":"variation","strand":1,"end":140442541,"alleles":["G","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442541},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799846782","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442542,"feature_type":"variation","strand":1,"end":140442542,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs1799846808","clinical_significance":[],"start":140442547,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","G"],"end":140442547,"strand":1,"feature_type":"variation"},{"end":140442550,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140442550,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585449255"},{"seq_region_name":"7","id":"rs1198035203","clinical_significance":[],"alleles":["C","T"],"end":140442551,"strand":1,"feature_type":"variation","start":140442551,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1799846869","clinical_significance":[],"end":140442553,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140442553,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"source":"dbSNP","start":140442554,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140442554,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1412685744"},{"start":140442555,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140442555,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799846929","clinical_significance":[]},{"seq_region_name":"7","id":"rs985613470","clinical_significance":[],"start":140442560,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140442560,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442561,"source":"dbSNP","strand":1,"feature_type":"variation","end":140442561,"alleles":["C","T"],"seq_region_name":"7","id":"rs1799846982","clinical_significance":[]},{"id":"rs1254735620","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442571,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140442571},{"seq_region_name":"7","id":"rs1799847017","clinical_significance":[],"start":140442574,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140442574,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"end":140442575,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140442575,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs915103381"},{"start":140442577,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","T"],"end":140442577,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs77204338","clinical_significance":[]},{"alleles":["C","T"],"end":140442578,"strand":1,"feature_type":"variation","start":140442578,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs767677960","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140442579,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442579,"clinical_significance":[],"seq_region_name":"7","id":"rs1344318316"},{"id":"rs76187221","seq_region_name":"7","clinical_significance":[],"start":140442580,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140442580,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs78255142","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442581,"feature_type":"variation","strand":1,"end":140442581,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs75234461","end":140442582,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140442582,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1799847193","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442583,"source":"dbSNP","strand":1,"feature_type":"variation","end":140442583,"alleles":["G","A"]},{"clinical_significance":[],"id":"rs1401394621","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140442585,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442585},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442586,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140442586,"clinical_significance":[],"seq_region_name":"7","id":"rs1294404450"},{"source":"dbSNP","start":140442587,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140442587,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1042341490"},{"seq_region_name":"7","id":"rs923832889","clinical_significance":[],"alleles":["C","T"],"end":140442589,"strand":1,"feature_type":"variation","start":140442589,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"id":"rs1415148422","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140442593,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442593,"source":"dbSNP"},{"seq_region_name":"7","id":"rs934653082","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442594,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140442594},{"seq_region_name":"7","id":"rs1403229560","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442596,"source":"dbSNP","strand":1,"feature_type":"variation","end":140442596,"alleles":["C","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799847367","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140442597,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442597},{"strand":1,"feature_type":"variation","end":140442598,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442598,"source":"dbSNP","seq_region_name":"7","id":"rs992090370","clinical_significance":[]},{"id":"rs916680966","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140442599,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442599,"source":"dbSNP"},{"seq_region_name":"7","id":"rs948099222","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442602,"source":"dbSNP","strand":1,"feature_type":"variation","end":140442602,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1057099931","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442603,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140442603},{"id":"rs1476933891","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442603,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GCT","-"],"end":140442605},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799847516","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442604,"feature_type":"variation","strand":1,"end":140442604,"alleles":["C","T"]},{"end":140442610,"alleles":["TTGTTT","TT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140442605,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1563081024","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1188967048","feature_type":"variation","strand":1,"end":140442613,"alleles":["TTTTTT","TTTTT"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442608},{"clinical_significance":[],"id":"rs1799847590","seq_region_name":"7","end":140442621,"alleles":["TTTTTACTTTTTA","TTTTTA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140442609,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"id":"rs2130206412","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140442613,"strand":1,"feature_type":"variation","start":140442613,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"start":140442623,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140442623,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs1799847617","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs895799096","seq_region_name":"7","alleles":["C","T"],"end":140442625,"feature_type":"variation","strand":1,"source":"dbSNP","start":140442625,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"end":140442630,"alleles":["T","C","G"],"strand":1,"feature_type":"variation","start":140442630,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs376888721","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799847703","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442633,"source":"dbSNP","strand":1,"feature_type":"variation","end":140442633,"alleles":["A","G"]},{"source":"dbSNP","start":140442639,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140442639,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799847723"},{"start":140442640,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140442640,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799847758","clinical_significance":[]},{"clinical_significance":[],"id":"rs1305323089","seq_region_name":"7","alleles":["A","G"],"end":140442643,"feature_type":"variation","strand":1,"source":"dbSNP","start":140442643,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"start":140442644,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140442644,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1200329867","clinical_significance":[]},{"source":"dbSNP","start":140442645,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","C","G"],"end":140442645,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799847807","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799847851","clinical_significance":[],"start":140442648,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140442648,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"start":140442649,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140442649,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","id":"rs1013040290","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1044854476","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442650,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140442650},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799847927","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442653,"feature_type":"variation","strand":1,"end":140442653,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1799847943","clinical_significance":[],"alleles":["T","C"],"end":140442655,"strand":1,"feature_type":"variation","start":140442655,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442659,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140442659,"seq_region_name":"7","id":"rs1340691387","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442660,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140442660,"id":"rs1799847980","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799847997","end":140442665,"alleles":["GAAGAA","GAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140442660,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442664,"feature_type":"variation","strand":1,"end":140442664,"alleles":["A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799848023"},{"id":"rs1251343865","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140442666,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442666,"source":"dbSNP"},{"source":"dbSNP","start":140442667,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140442667,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799848050"},{"source":"dbSNP","start":140442668,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140442668,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs888641994","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140442669,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442669,"clinical_significance":[],"id":"rs1315583008","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799848117","source":"dbSNP","start":140442675,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140442675,"alleles":["T","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs930132974","clinical_significance":[],"strand":1,"feature_type":"variation","end":140442679,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442679,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1233582823","clinical_significance":[],"start":140442684,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","C"],"end":140442684,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442686,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140442686,"id":"rs1047334442","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs891359421","seq_region_name":"7","end":140442687,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140442687,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs538410325","clinical_significance":[],"end":140442688,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140442688,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"id":"rs10275142","seq_region_name":"7","source":"dbSNP","start":140442692,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","A","C"],"end":140442692,"feature_type":"variation","strand":1},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442693,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140442693,"clinical_significance":[],"seq_region_name":"7","id":"rs2130206570"},{"clinical_significance":[],"seq_region_name":"7","id":"rs61043891","source":"dbSNP","start":140442708,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140442708,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442716,"source":"dbSNP","strand":1,"feature_type":"variation","end":140442716,"alleles":["G","A"],"seq_region_name":"7","id":"rs1464101694","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs900257303","feature_type":"variation","strand":1,"end":140442722,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442722},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799848439","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442723,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140442723},{"seq_region_name":"7","id":"rs995893783","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442730,"source":"dbSNP","strand":1,"feature_type":"variation","end":140442730,"alleles":["C","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1022048761","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140442731,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442731},{"source":"dbSNP","start":140442733,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["AT","-"],"end":140442734,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1221121113"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442735,"source":"dbSNP","strand":1,"feature_type":"variation","end":140442735,"alleles":["G","A"],"seq_region_name":"7","id":"rs1799848513","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130206636","alleles":["T","C"],"end":140442736,"feature_type":"variation","strand":1,"source":"dbSNP","start":140442736,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1799848530","clinical_significance":[],"strand":1,"feature_type":"variation","end":140442739,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442739,"source":"dbSNP"},{"seq_region_name":"7","id":"rs536801908","clinical_significance":[],"end":140442741,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140442741,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1799848593","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442742,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140442742},{"seq_region_name":"7","id":"rs2130206654","clinical_significance":[],"start":140442751,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140442751,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442754,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140442754,"clinical_significance":[],"seq_region_name":"7","id":"rs538654932"},{"seq_region_name":"7","id":"rs1438853904","clinical_significance":[],"alleles":["T","C"],"end":140442758,"strand":1,"feature_type":"variation","start":140442758,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"alleles":["T","-"],"end":140442758,"strand":1,"feature_type":"variation","start":140442758,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799848661","clinical_significance":[]},{"source":"dbSNP","start":140442760,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140442760,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs961566971","seq_region_name":"7"},{"id":"rs1799848703","seq_region_name":"7","clinical_significance":[],"alleles":["A","G"],"end":140442763,"strand":1,"feature_type":"variation","start":140442763,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442765,"feature_type":"variation","strand":1,"end":140442765,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1251863791"},{"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140442766,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442766,"clinical_significance":[],"seq_region_name":"7","id":"rs760806229"},{"seq_region_name":"7","id":"rs2130206693","clinical_significance":[],"start":140442770,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","A"],"end":140442770,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1799848777","seq_region_name":"7","source":"dbSNP","start":140442771,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140442771,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1799848798","clinical_significance":[],"start":140442772,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","C"],"end":140442772,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs768377576","clinical_significance":[],"start":140442774,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140442779,"alleles":["TTTTTT","TTTTTTT"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1256881105","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140442775,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442775,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140442783,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442783,"source":"dbSNP","seq_region_name":"7","id":"rs1029370481","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442786,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140442786,"clinical_significance":[],"seq_region_name":"7","id":"rs999751042"},{"clinical_significance":[],"id":"rs1799848926","seq_region_name":"7","feature_type":"variation","strand":1,"end":140442789,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442789},{"clinical_significance":[],"seq_region_name":"7","id":"rs1358061073","alleles":["C","CC"],"end":140442794,"feature_type":"variation","strand":1,"source":"dbSNP","start":140442794,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs953826237","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442798,"source":"dbSNP","strand":1,"feature_type":"variation","end":140442798,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799848979","source":"dbSNP","start":140442800,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140442800,"alleles":["T","G"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140442802,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442802,"source":"dbSNP","seq_region_name":"7","id":"rs985256496","clinical_significance":[]},{"alleles":["T","C"],"end":140442813,"feature_type":"variation","strand":1,"source":"dbSNP","start":140442813,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130206735"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140442825,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442825,"source":"dbSNP","seq_region_name":"7","id":"rs1585449407","clinical_significance":[]},{"clinical_significance":[],"id":"rs914966031","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442827,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140442827},{"alleles":["T","G"],"end":140442828,"strand":1,"feature_type":"variation","start":140442828,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1026178324","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442833,"source":"dbSNP","strand":1,"feature_type":"variation","end":140442833,"alleles":["C","T"],"seq_region_name":"7","id":"rs967894176","clinical_significance":[]},{"end":140442835,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140442835,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1243766938"},{"source":"dbSNP","start":140442836,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140442836,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs377148781"},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140442837,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442837,"clinical_significance":[],"seq_region_name":"7","id":"rs1799849205"},{"clinical_significance":[],"id":"rs1799849232","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442840,"feature_type":"variation","strand":1,"end":140442840,"alleles":["G","A"]},{"id":"rs1311362715","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442842,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140442842},{"strand":1,"feature_type":"variation","end":140442851,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442851,"source":"dbSNP","seq_region_name":"7","id":"rs1799849272","clinical_significance":[]},{"source":"dbSNP","start":140442852,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","A","C"],"end":140442852,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799849292"},{"feature_type":"variation","strand":1,"end":140442854,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442854,"clinical_significance":[],"seq_region_name":"7","id":"rs1693022207"},{"clinical_significance":[],"seq_region_name":"7","id":"rs554659256","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442856,"feature_type":"variation","strand":1,"end":140442856,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1799849331","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140442857,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442857,"source":"dbSNP"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442858,"feature_type":"variation","strand":1,"end":140442858,"alleles":["T","C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs960883205"},{"clinical_significance":[],"id":"rs573154196","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442864,"feature_type":"variation","strand":1,"end":140442864,"alleles":["A","C"]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140442867,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442867,"source":"dbSNP","seq_region_name":"7","id":"rs114163368","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140442869,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442869,"source":"dbSNP","seq_region_name":"7","id":"rs1799849454","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799849473","clinical_significance":[],"alleles":["A","G"],"end":140442870,"strand":1,"feature_type":"variation","start":140442870,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799849494","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442871,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140442871},{"start":140442872,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","A","T"],"end":140442872,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs79934404","clinical_significance":[]},{"start":140442873,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A","C"],"end":140442873,"strand":1,"feature_type":"variation","id":"rs145291580","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","C"],"end":140442874,"feature_type":"variation","strand":1,"source":"dbSNP","start":140442874,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1371178669"},{"clinical_significance":[],"seq_region_name":"7","id":"rs930189246","source":"dbSNP","start":140442875,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140442875,"alleles":["A","T"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140442877,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442877,"clinical_significance":[],"seq_region_name":"7","id":"rs1799849673"},{"source":"dbSNP","start":140442878,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140442878,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs563105050"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442880,"source":"dbSNP","strand":1,"feature_type":"variation","end":140442881,"alleles":["CT","-"],"id":"rs1799849718","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140442882,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140442882,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799849731","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140442886,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442886,"clinical_significance":[],"seq_region_name":"7","id":"rs1439625124"},{"id":"rs983327582","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442888,"source":"dbSNP","strand":1,"feature_type":"variation","end":140442888,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs1221686071","clinical_significance":[],"end":140442894,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140442894,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442905,"feature_type":"variation","strand":1,"end":140442905,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1452882044"},{"clinical_significance":[],"seq_region_name":"7","id":"rs912833471","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442907,"feature_type":"variation","strand":1,"alleles":["GG","G"],"end":140442908},{"seq_region_name":"7","id":"rs1799849852","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442913,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140442913},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442917,"source":"dbSNP","strand":1,"feature_type":"variation","end":140442917,"alleles":["A","G"],"seq_region_name":"7","id":"rs2130206906","clinical_significance":[]},{"seq_region_name":"7","id":"rs1563081082","clinical_significance":[],"strand":1,"feature_type":"variation","end":140442918,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442918,"source":"dbSNP"},{"id":"rs1208939107","seq_region_name":"7","clinical_significance":[],"alleles":["A","G"],"end":140442922,"strand":1,"feature_type":"variation","start":140442922,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"end":140442926,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140442926,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs555200364","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs183824206","feature_type":"variation","strand":1,"end":140442927,"alleles":["G","A","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442927},{"seq_region_name":"7","id":"rs147231049","clinical_significance":[],"start":140442928,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","A","C"],"end":140442928,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140442934,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442934,"clinical_significance":[],"seq_region_name":"7","id":"rs1304193758"},{"strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140442940,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442940,"source":"dbSNP","seq_region_name":"7","id":"rs796071811","clinical_significance":[]},{"end":140442946,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140442946,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs888507158","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799850060","source":"dbSNP","start":140442951,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140442951,"alleles":["T","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs900205112","seq_region_name":"7","feature_type":"variation","strand":1,"end":140442952,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442952},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442956,"feature_type":"variation","strand":1,"alleles":["TGGGCGTGGTGGTGGGCG","TGGGCG"],"end":140442973,"clinical_significance":[],"seq_region_name":"7","id":"rs1799850098"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799850116","end":140442959,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140442959,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140442960,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140442960,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1005677547"},{"seq_region_name":"7","id":"rs1323140907","clinical_significance":[],"end":140442961,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140442961,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585449518","end":140442963,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140442963,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs750375091","source":"dbSNP","start":140442965,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140442965,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs931635883","clinical_significance":[],"start":140442966,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140442966,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"alleles":["GG","G"],"end":140442967,"feature_type":"variation","strand":1,"source":"dbSNP","start":140442966,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799850254"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442969,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140442969,"clinical_significance":[],"seq_region_name":"7","id":"rs1157259417"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442971,"feature_type":"variation","strand":1,"alleles":["G","C","T"],"end":140442971,"clinical_significance":[],"seq_region_name":"7","id":"rs1396183391"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442972,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140442972,"clinical_significance":[],"seq_region_name":"7","id":"rs1193466361"},{"clinical_significance":[],"seq_region_name":"7","id":"rs188488738","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442973,"feature_type":"variation","strand":1,"end":140442973,"alleles":["G","A"]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140442977,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442977,"clinical_significance":[],"seq_region_name":"7","id":"rs191918583"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1197647671","feature_type":"variation","strand":1,"end":140442980,"alleles":["A","C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442980},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140442981,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140442981,"seq_region_name":"7","id":"rs1488416559","clinical_significance":[]},{"alleles":["T","C"],"end":140442988,"feature_type":"variation","strand":1,"source":"dbSNP","start":140442988,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585449546"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799850672","source":"dbSNP","start":140442992,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140442992,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799850692","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140442993,"feature_type":"variation","strand":1,"end":140442993,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1287843395","clinical_significance":[],"start":140442995,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140442995,"strand":1,"feature_type":"variation"},{"id":"rs1799850725","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140442997,"strand":1,"feature_type":"variation","start":140442997,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799850741","source":"dbSNP","start":140442998,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140442998,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443001,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140443001,"seq_region_name":"7","id":"rs1799850768","clinical_significance":[]},{"end":140443002,"alleles":["A","ACA"],"strand":1,"feature_type":"variation","start":140443002,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799850784","clinical_significance":[]},{"seq_region_name":"7","id":"rs1563081108","clinical_significance":[],"start":140443006,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140443007,"alleles":["AA","-"],"strand":1,"feature_type":"variation"},{"end":140443009,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140443009,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs374013275","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1201783569","clinical_significance":[],"alleles":["G","T"],"end":140443010,"strand":1,"feature_type":"variation","start":140443010,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"start":140443019,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140443019,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799850889","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140443022,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443022,"source":"dbSNP","seq_region_name":"7","id":"rs571190125","clinical_significance":[]},{"end":140443022,"alleles":["C","-"],"strand":1,"feature_type":"variation","start":140443022,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1232278652","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443024,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140443024,"clinical_significance":[],"seq_region_name":"7","id":"rs1342948838"},{"seq_region_name":"7","id":"rs896410579","clinical_significance":[],"strand":1,"feature_type":"variation","end":140443025,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443025,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140443029,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443029,"clinical_significance":[],"seq_region_name":"7","id":"rs1799851008"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443031,"feature_type":"variation","strand":1,"end":140443031,"alleles":["C","T"],"clinical_significance":[],"id":"rs1483506248","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140443032,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443032,"clinical_significance":[],"seq_region_name":"7","id":"rs1342630814"},{"end":140443034,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140443034,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1013489487"},{"seq_region_name":"7","id":"rs1399747648","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443035,"source":"dbSNP","strand":1,"feature_type":"variation","end":140443035,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585449594","feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140443037,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443037},{"strand":1,"feature_type":"variation","end":140443040,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443040,"source":"dbSNP","seq_region_name":"7","id":"rs1183407209","clinical_significance":[]},{"id":"rs148711335","seq_region_name":"7","clinical_significance":[],"end":140443041,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140443041,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"id":"rs1799851234","seq_region_name":"7","alleles":["A","G"],"end":140443042,"feature_type":"variation","strand":1,"source":"dbSNP","start":140443042,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs566003391","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443048,"source":"dbSNP","strand":1,"feature_type":"variation","end":140443048,"alleles":["T","A"]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443049,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GAGA","GAGAGA"],"end":140443052,"seq_region_name":"7","id":"rs1799851270","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140443051,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443051,"source":"dbSNP","seq_region_name":"7","id":"rs1178851966","clinical_significance":[]},{"seq_region_name":"7","id":"rs969384720","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443056,"source":"dbSNP","strand":1,"feature_type":"variation","end":140443056,"alleles":["C","T"]},{"end":140443057,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140443057,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1443024483","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs953750185","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140443059,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443059},{"seq_region_name":"7","id":"rs1799851560","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443063,"source":"dbSNP","strand":1,"feature_type":"variation","end":140443063,"alleles":["G","C"]},{"seq_region_name":"7","id":"rs1006944264","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443064,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140443064},{"source":"dbSNP","start":140443068,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140443068,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1477916028","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs974031919","feature_type":"variation","strand":1,"end":140443072,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443072},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799851641","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443074,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140443074},{"clinical_significance":[],"seq_region_name":"7","id":"rs1391010654","alleles":["G","C","T"],"end":140443076,"feature_type":"variation","strand":1,"source":"dbSNP","start":140443076,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"start":140443081,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","-"],"end":140443081,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799851759","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799851776","alleles":["A","G"],"end":140443085,"feature_type":"variation","strand":1,"source":"dbSNP","start":140443085,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1585449634","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443088,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AAAA","AA"],"end":140443091},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443091,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140443091,"seq_region_name":"7","id":"rs1027083848","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443092,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140443092,"clinical_significance":[],"seq_region_name":"7","id":"rs1799851840"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1411769044","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443094,"feature_type":"variation","strand":1,"end":140443094,"alleles":["C","A"]},{"seq_region_name":"7","id":"rs1212082459","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443098,"source":"dbSNP","strand":1,"feature_type":"variation","end":140443098,"alleles":["C","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1440658946","end":140443100,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140443100,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443100,"feature_type":"variation","strand":1,"alleles":["C","-"],"end":140443100,"clinical_significance":[],"seq_region_name":"7","id":"rs1799851920"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443101,"source":"dbSNP","strand":1,"feature_type":"variation","end":140443101,"alleles":["A","C"],"seq_region_name":"7","id":"rs1585449643","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443101,"source":"dbSNP","strand":1,"feature_type":"variation","end":140443112,"alleles":["AAAAAAAAAAAA","AAAAAAAAA","AAAAAAAAAA","AAAAAAAAAAA","AAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAA"],"seq_region_name":"7","id":"rs58324377","clinical_significance":[]},{"id":"rs1022058648","seq_region_name":"7","clinical_significance":[],"alleles":["A","C"],"end":140443104,"strand":1,"feature_type":"variation","start":140443104,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140443107,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443107,"clinical_significance":[],"id":"rs1168393820","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1354490656","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443113,"source":"dbSNP","strand":1,"feature_type":"variation","end":140443113,"alleles":["T","-"]},{"clinical_significance":[],"id":"rs1799852158","seq_region_name":"7","source":"dbSNP","start":140443113,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140443113,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140443114,"alleles":["C","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443114,"clinical_significance":[],"seq_region_name":"7","id":"rs550356198"},{"feature_type":"variation","strand":1,"end":140443116,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443116,"clinical_significance":[],"seq_region_name":"7","id":"rs1218313820"},{"id":"rs78311280","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443120,"source":"dbSNP","strand":1,"feature_type":"variation","end":140443120,"alleles":["G","C"]},{"start":140443121,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["TATTAATA","TA"],"end":140443128,"strand":1,"feature_type":"variation","id":"rs1799852279","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140443122,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140443122,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799852301"},{"seq_region_name":"7","id":"rs1304964700","clinical_significance":[],"start":140443123,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140443123,"alleles":["T","A","C"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140443134,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140443134,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs977829634"},{"end":140443135,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140443135,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799852373"},{"start":140443138,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140443138,"alleles":["G","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799852401","clinical_significance":[]},{"seq_region_name":"7","id":"rs923811504","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443146,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140443146},{"seq_region_name":"7","id":"rs1799852437","clinical_significance":[],"strand":1,"feature_type":"variation","end":140443147,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443147,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443153,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140443153,"seq_region_name":"7","id":"rs1585449680","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1359118407","end":140443154,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140443154,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140443158,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140443158,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1330205185"},{"clinical_significance":[],"seq_region_name":"7","id":"rs982974378","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443163,"feature_type":"variation","strand":1,"end":140443163,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs912689342","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443165,"source":"dbSNP","strand":1,"feature_type":"variation","end":140443165,"alleles":["C","T"]},{"id":"rs2130207428","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140443170,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443170,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140443188,"alleles":["CAGTTACTATGTCCCAG","CAG"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443172,"source":"dbSNP","seq_region_name":"7","id":"rs756681281","clinical_significance":[]},{"end":140443177,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140443177,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs10272040"},{"feature_type":"variation","strand":1,"end":140443180,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443180,"clinical_significance":[],"seq_region_name":"7","id":"rs975704247"},{"strand":1,"feature_type":"variation","end":140443181,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443181,"source":"dbSNP","seq_region_name":"7","id":"rs1799852713","clinical_significance":[]},{"clinical_significance":[],"id":"rs1380969019","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["TGTCCCAG","TGTCCCAGTGTCCCAG"],"end":140443188,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443181},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443184,"source":"dbSNP","strand":1,"feature_type":"variation","end":140443184,"alleles":["C","T"],"seq_region_name":"7","id":"rs1799852792","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs10272047","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140443195,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443195},{"id":"rs1799852895","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140443203,"strand":1,"feature_type":"variation","start":140443203,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"id":"rs777980934","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["TTAATTTA","TTA"],"end":140443211,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443204,"source":"dbSNP"},{"end":140443212,"alleles":["ATTTAT","AT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140443207,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799852941"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1236795849","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140443213,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443213},{"feature_type":"variation","strand":1,"end":140443215,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443215,"clinical_significance":[],"seq_region_name":"7","id":"rs2130207516"},{"source":"dbSNP","start":140443218,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G","T"],"end":140443218,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs754534397"},{"feature_type":"variation","strand":1,"end":140443224,"alleles":["TTTT","TTT"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443221,"clinical_significance":[],"seq_region_name":"7","id":"rs1199266057"},{"feature_type":"variation","strand":1,"end":140443224,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443224,"clinical_significance":[],"seq_region_name":"7","id":"rs948765174"},{"seq_region_name":"7","id":"rs1341007231","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443225,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140443225},{"end":140443228,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140443228,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799853083"},{"seq_region_name":"7","id":"rs1799853102","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443230,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140443230},{"clinical_significance":[],"seq_region_name":"7","id":"rs980470156","source":"dbSNP","start":140443241,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140443241,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs931645806","seq_region_name":"7","source":"dbSNP","start":140443245,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140443245,"feature_type":"variation","strand":1},{"alleles":["A","G"],"end":140443250,"strand":1,"feature_type":"variation","start":140443250,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs909978232","clinical_significance":[]},{"start":140443261,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140443261,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799853236","clinical_significance":[]},{"id":"rs1322588020","seq_region_name":"7","clinical_significance":[],"start":140443271,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140443271,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1271625083","clinical_significance":[],"start":140443272,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140443272,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443277,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AGAGA","AGA"],"end":140443281,"seq_region_name":"7","id":"rs1799853301","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs925058117","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140443282,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443282},{"seq_region_name":"7","id":"rs1799853349","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443283,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140443283},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799853367","alleles":["A","T"],"end":140443287,"feature_type":"variation","strand":1,"source":"dbSNP","start":140443287,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"start":140443288,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140443288,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799853389","clinical_significance":[]},{"source":"dbSNP","start":140443289,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140443289,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799853405"},{"clinical_significance":[],"id":"rs1205420799","seq_region_name":"7","end":140443290,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140443290,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"end":140443301,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140443301,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1378953397","seq_region_name":"7"},{"source":"dbSNP","start":140443303,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140443303,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs76423640"},{"start":140443305,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140443305,"strand":1,"feature_type":"variation","id":"rs1037060685","seq_region_name":"7","clinical_significance":[]},{"start":140443311,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140443311,"alleles":["C","G"],"strand":1,"feature_type":"variation","id":"rs2130207637","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1013353922","source":"dbSNP","start":140443320,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140443320,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1464732380","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443323,"feature_type":"variation","strand":1,"end":140443325,"alleles":["AAA","AAAA"]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443324,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140443324,"seq_region_name":"7","id":"rs1350083691","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443327,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140443327,"clinical_significance":[],"seq_region_name":"7","id":"rs1799853642"},{"seq_region_name":"7","id":"rs1799853666","clinical_significance":[],"end":140443331,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140443331,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs897358441","clinical_significance":[],"start":140443332,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140443332,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"alleles":["A","G"],"end":140443333,"feature_type":"variation","strand":1,"source":"dbSNP","start":140443333,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1166517873","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1421825813","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443334,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140443334},{"strand":1,"feature_type":"variation","end":140443341,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443341,"source":"dbSNP","seq_region_name":"7","id":"rs1799853740","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443365,"source":"dbSNP","strand":1,"feature_type":"variation","end":140443365,"alleles":["T","G"],"seq_region_name":"7","id":"rs934124545","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1412872192","alleles":["T","C"],"end":140443368,"feature_type":"variation","strand":1,"source":"dbSNP","start":140443368,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140443370,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443370,"clinical_significance":[],"seq_region_name":"7","id":"rs1051370358"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1179114098","end":140443373,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140443373,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1441468827","seq_region_name":"7","alleles":["G","A"],"end":140443378,"feature_type":"variation","strand":1,"source":"dbSNP","start":140443378,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443382,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140443382,"seq_region_name":"7","id":"rs534148484","clinical_significance":[]},{"clinical_significance":[],"id":"rs1178128024","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443386,"feature_type":"variation","strand":1,"end":140443386,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1044989761","end":140443389,"alleles":["-","GA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140443390,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1006568045","source":"dbSNP","start":140443392,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140443392,"feature_type":"variation","strand":1},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443400,"feature_type":"variation","strand":1,"end":140443400,"alleles":["C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs142291192"},{"end":140443403,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140443403,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799854013","clinical_significance":[]},{"start":140443404,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","A","T"],"end":140443404,"strand":1,"feature_type":"variation","id":"rs747834934","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443405,"source":"dbSNP","strand":1,"feature_type":"variation","end":140443405,"alleles":["A","T"],"seq_region_name":"7","id":"rs1476486041","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443407,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140443407,"id":"rs1799854096","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799854125","end":140443408,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140443408,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"id":"rs1799854140","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140443415,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443415,"source":"dbSNP"},{"id":"rs184479862","seq_region_name":"7","clinical_significance":[],"alleles":["G","A","C"],"end":140443420,"strand":1,"feature_type":"variation","start":140443420,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs951504735","alleles":["C","T"],"end":140443422,"feature_type":"variation","strand":1,"source":"dbSNP","start":140443422,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443423,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140443423,"seq_region_name":"7","id":"rs1799854217","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443424,"feature_type":"variation","strand":1,"alleles":["AGAAGA","AGA"],"end":140443429,"clinical_significance":[],"seq_region_name":"7","id":"rs533001214"},{"clinical_significance":[],"id":"rs1799854271","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140443427,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443427},{"seq_region_name":"7","id":"rs1799854291","clinical_significance":[],"strand":1,"feature_type":"variation","end":140443433,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443433,"source":"dbSNP"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443436,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140443436,"clinical_significance":[],"id":"rs1799854314","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799854332","alleles":["A","G"],"end":140443437,"feature_type":"variation","strand":1,"source":"dbSNP","start":140443437,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1019695231","clinical_significance":[],"strand":1,"feature_type":"variation","end":140443440,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443440,"source":"dbSNP"},{"id":"rs1799854365","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140443441,"strand":1,"feature_type":"variation","start":140443441,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"alleles":["G","A","C"],"end":140443446,"strand":1,"feature_type":"variation","start":140443446,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs537387140","clinical_significance":[]},{"source":"dbSNP","start":140443453,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140443453,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799854401","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1390277544","alleles":["C","A","G"],"end":140443454,"feature_type":"variation","strand":1,"source":"dbSNP","start":140443454,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130207849","source":"dbSNP","start":140443455,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140443455,"alleles":["T","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1294909666","clinical_significance":[],"start":140443456,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140443456,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1456076191","alleles":["C","T"],"end":140443459,"feature_type":"variation","strand":1,"source":"dbSNP","start":140443459,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1349020360","seq_region_name":"7","feature_type":"variation","strand":1,"end":140443461,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443461},{"id":"rs965562572","seq_region_name":"7","clinical_significance":[],"end":140443462,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140443462,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs975547423","alleles":["C","G","T"],"end":140443463,"feature_type":"variation","strand":1,"source":"dbSNP","start":140443463,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"start":140443467,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140443467,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1378383164","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443468,"feature_type":"variation","strand":1,"end":140443468,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1179286144"},{"id":"rs1799854599","seq_region_name":"7","clinical_significance":[],"alleles":["G","A","T"],"end":140443470,"strand":1,"feature_type":"variation","start":140443470,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443472,"source":"dbSNP","strand":1,"feature_type":"variation","end":140443472,"alleles":["T","C"],"seq_region_name":"7","id":"rs1799854624","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799854649","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443473,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140443473},{"id":"rs964847848","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443476,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140443476},{"clinical_significance":[],"seq_region_name":"7","id":"rs1030741921","feature_type":"variation","strand":1,"end":140443478,"alleles":["C","A","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443478},{"seq_region_name":"7","id":"rs1404534086","clinical_significance":[],"start":140443480,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140443480,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443481,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140443481,"clinical_significance":[],"seq_region_name":"7","id":"rs960582427"},{"seq_region_name":"7","id":"rs1585449845","clinical_significance":[],"alleles":["C","T"],"end":140443482,"strand":1,"feature_type":"variation","start":140443482,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs544969989","clinical_significance":[],"strand":1,"feature_type":"variation","end":140443485,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443485,"source":"dbSNP"},{"start":140443488,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140443488,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1469653088","clinical_significance":[]},{"start":140443491,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","C"],"end":140443491,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs921530241","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799854869","feature_type":"variation","strand":1,"end":140443496,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443496},{"feature_type":"variation","strand":1,"end":140443498,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443498,"clinical_significance":[],"id":"rs992375984","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799854905","alleles":["A","C"],"end":140443502,"feature_type":"variation","strand":1,"source":"dbSNP","start":140443502,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799854922","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443506,"feature_type":"variation","strand":1,"end":140443506,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1269637685","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443509,"feature_type":"variation","strand":1,"end":140443509,"alleles":["A","G"]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140443513,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443513,"clinical_significance":[],"seq_region_name":"7","id":"rs1799854965"},{"seq_region_name":"7","id":"rs1585449864","clinical_significance":[],"alleles":["T","G"],"end":140443514,"strand":1,"feature_type":"variation","start":140443514,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799855015","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443515,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140443515},{"end":140443521,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140443521,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1189638621","clinical_significance":[]},{"end":140443525,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140443525,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1488282898","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799855073","end":140443530,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140443530,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1799855089","clinical_significance":[],"alleles":["A","C","G"],"end":140443532,"strand":1,"feature_type":"variation","start":140443532,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799855112","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140443533,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443533},{"alleles":["T","G"],"end":140443534,"strand":1,"feature_type":"variation","start":140443534,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs968918397","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799855161","feature_type":"variation","strand":1,"end":140443544,"alleles":["GCTGCTG","GCTG"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443538},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140443539,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443539,"clinical_significance":[],"id":"rs1321578836","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443543,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","-"],"end":140443543,"seq_region_name":"7","id":"rs1327858340","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799855252","seq_region_name":"7","feature_type":"variation","strand":1,"end":140443545,"alleles":["G","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443545},{"id":"rs1585449889","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443546,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140443546},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443551,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140443551,"id":"rs1023554792","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443552,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140443552,"seq_region_name":"7","id":"rs1285918556","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs979127499","source":"dbSNP","start":140443553,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140443553,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140443555,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443555,"clinical_significance":[],"id":"rs1428128881","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799855363","clinical_significance":[],"alleles":["G","C"],"end":140443560,"strand":1,"feature_type":"variation","start":140443560,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"id":"rs2130208035","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443569,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140443569},{"clinical_significance":[],"seq_region_name":"7","id":"rs924973567","source":"dbSNP","start":140443570,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140443570,"alleles":["T","C"],"feature_type":"variation","strand":1},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443574,"feature_type":"variation","strand":1,"end":140443574,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130208045"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443575,"source":"dbSNP","strand":1,"feature_type":"variation","end":140443575,"alleles":["C","T"],"id":"rs1799855412","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs151251481","feature_type":"variation","strand":1,"end":140443578,"alleles":["G","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443578},{"clinical_significance":[],"id":"rs140482599","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443579,"feature_type":"variation","strand":1,"end":140443579,"alleles":["G","A","C","T"]},{"strand":1,"feature_type":"variation","end":140443581,"alleles":["GAG","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443579,"source":"dbSNP","seq_region_name":"7","id":"rs2130208078","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799855509","clinical_significance":[],"start":140443581,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["GG","G"],"end":140443582,"strand":1,"feature_type":"variation"},{"end":140443583,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140443583,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs375981175","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140443584,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443584,"source":"dbSNP","seq_region_name":"7","id":"rs1224812422","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585449926","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443589,"source":"dbSNP","strand":1,"feature_type":"variation","end":140443589,"alleles":["T","C","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1157919335","feature_type":"variation","strand":1,"alleles":["TT","-"],"end":140443590,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443589},{"strand":1,"feature_type":"variation","end":140443592,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443592,"source":"dbSNP","seq_region_name":"7","id":"rs1799855615","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1466504895","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140443600,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443600},{"seq_region_name":"7","id":"rs941353554","clinical_significance":[],"start":140443601,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140443601,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1174088168","clinical_significance":[],"alleles":["A","T"],"end":140443604,"strand":1,"feature_type":"variation","start":140443604,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"id":"rs1424563859","seq_region_name":"7","feature_type":"variation","strand":1,"end":140443605,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443605},{"alleles":["TCGCACTACT","T"],"end":140443614,"strand":1,"feature_type":"variation","start":140443605,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1432720504","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140443606,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443606,"source":"dbSNP","seq_region_name":"7","id":"rs972806256","clinical_significance":[]},{"source":"dbSNP","start":140443607,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140443607,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs561000505","seq_region_name":"7"},{"id":"rs190352062","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443612,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140443612},{"id":"rs1799855791","seq_region_name":"7","clinical_significance":[],"start":140443614,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","A"],"end":140443614,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799855817","source":"dbSNP","start":140443615,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140443615,"alleles":["G","GG"],"feature_type":"variation","strand":1},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443616,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140443616,"clinical_significance":[],"id":"rs1799855837","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140443621,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443621,"source":"dbSNP","seq_region_name":"7","id":"rs1262935938","clinical_significance":[]},{"clinical_significance":[],"id":"rs917652901","seq_region_name":"7","source":"dbSNP","start":140443629,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140443629,"feature_type":"variation","strand":1},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443632,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140443632,"clinical_significance":[],"seq_region_name":"7","id":"rs2130208170"},{"seq_region_name":"7","id":"rs918643832","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443634,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140443634},{"end":140443637,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140443637,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799855938"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443638,"feature_type":"variation","strand":1,"end":140443638,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799855956"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443640,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140443640,"clinical_significance":[],"seq_region_name":"7","id":"rs1799855972"},{"source":"dbSNP","start":140443643,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140443646,"alleles":["CTCT","CT"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs747129312"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1448961103","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443648,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140443648},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799856030","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443650,"feature_type":"variation","strand":1,"end":140443650,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs777321310","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443652,"feature_type":"variation","strand":1,"alleles":["A","C","T"],"end":140443652},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799856067","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140443660,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443660},{"seq_region_name":"7","id":"rs577594412","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443662,"source":"dbSNP","strand":1,"feature_type":"variation","end":140443662,"alleles":["A","G"]},{"source":"dbSNP","start":140443663,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140443663,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799856148"},{"source":"dbSNP","start":140443669,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140443669,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1044853956"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1278437348","feature_type":"variation","strand":1,"end":140443676,"alleles":["AAAGAAA","AAA"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443670},{"source":"dbSNP","start":140443676,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140443676,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1220152396"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443687,"source":"dbSNP","strand":1,"feature_type":"variation","end":140443687,"alleles":["T","A"],"seq_region_name":"7","id":"rs1585449980","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799856263","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443698,"source":"dbSNP","strand":1,"feature_type":"variation","end":140443698,"alleles":["C","A"]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443702,"source":"dbSNP","strand":1,"feature_type":"variation","end":140443702,"alleles":["C","A","T"],"id":"rs1213842335","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799856302","source":"dbSNP","start":140443705,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140443705,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1799856325","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140443711,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443711,"source":"dbSNP"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443713,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140443713,"clinical_significance":[],"seq_region_name":"7","id":"rs749791738"},{"alleles":["C","T"],"end":140443715,"strand":1,"feature_type":"variation","start":140443715,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799856367","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs10952668","source":"dbSNP","start":140443720,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","A","G","T"],"end":140443720,"feature_type":"variation","strand":1},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443722,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140443722,"clinical_significance":[],"seq_region_name":"7","id":"rs1480844743"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799856513","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443725,"feature_type":"variation","strand":1,"alleles":["TTT","TT"],"end":140443727},{"id":"rs1799856531","seq_region_name":"7","clinical_significance":[],"alleles":["G","T"],"end":140443728,"strand":1,"feature_type":"variation","start":140443728,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799856563","end":140443730,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140443730,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"start":140443743,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140443743,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1201655156","clinical_significance":[]},{"start":140443745,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140443745,"strand":1,"feature_type":"variation","id":"rs1799856618","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1469348998","source":"dbSNP","start":140443746,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140443746,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140443750,"alleles":["CCTC","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443747,"source":"dbSNP","seq_region_name":"7","id":"rs1427839268","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140443748,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443748,"clinical_significance":[],"seq_region_name":"7","id":"rs1799856689"},{"seq_region_name":"7","id":"rs539818660","clinical_significance":[],"start":140443750,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140443750,"strand":1,"feature_type":"variation"},{"end":140443755,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140443755,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1476966577","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1480371094","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140443756,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443756},{"source":"dbSNP","start":140443759,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140443759,"alleles":["C","CC"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1160368730","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140443759,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443759,"source":"dbSNP","id":"rs1799856778","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443759,"feature_type":"variation","strand":1,"alleles":["CAACACA","CA"],"end":140443765,"clinical_significance":[],"id":"rs2130208351","seq_region_name":"7"},{"end":140443759,"alleles":["-","CA","CACA"],"strand":1,"feature_type":"variation","start":140443760,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1654981526","clinical_significance":[]},{"start":140443760,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140443760,"alleles":["A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1051668030","clinical_significance":[]},{"id":"rs1491423200","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443760,"source":"dbSNP","strand":1,"feature_type":"variation","end":140443761,"alleles":["AA","-"]},{"end":140443763,"alleles":["AACA","-"],"strand":1,"feature_type":"variation","start":140443760,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs766635566","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs748980197","source":"dbSNP","start":140443760,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140443765,"alleles":["AACACA","-"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140443760,"alleles":["-","CAC"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443761,"source":"dbSNP","seq_region_name":"7","id":"rs1799856920","clinical_significance":[]},{"id":"rs55700076","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443761,"source":"dbSNP","strand":1,"feature_type":"variation","end":140443808,"alleles":["ACACACACACACACACACACACACACACACACACACACACACACACAC","ACACACACACACACAC","ACACACACACACACACAC","ACACACACACACACACACAC","ACACACACACACACACACACAC","ACACACACACACACACACACACAC","ACACACACACACACACACACACACAC","ACACACACACACACACACACACACACAC","ACACACACACACACACACACACACACACAC","ACACACACACACACACACACACACACACACAC","ACACACACACACACACACACACACACACACACAC","ACACACACACACACACACACACACACACACACACAC","ACACACACACACACACACACACACACACACACACACAC","ACACACACACACACACACACACACACACACACACACACAC","ACACACACACACACACACACACACACACACACACACACACAC","ACACACACACACACACACACACACACACACACACACACACACAC","ACACACACACACACACACACACACACACACACACACACACACACAC","ACACACACACACACACACACACACACACACACACACACACACACACACAC","ACACACACACACACACACACACACACACACACACACACACACACACACACAC","ACACACACACACACACACACACACACACACACACACACACACACACACACACAC","ACACACACACACACACACACACACACACACACACACACACACACACACACACACAC","ACACACACACACACACACACACACACACACACACACACACACACACACACACACACAC","ACACACACACACACACACACACACACACACACACACACACACACACACACACACACACAC","ACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACAC","ACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACAC","ACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACAC","ACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACAC"]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443762,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140443762,"id":"rs1179999964","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","-"],"end":140443762,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443762,"source":"dbSNP","seq_region_name":"7","id":"rs1399307643","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140443763,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443763,"clinical_significance":[],"id":"rs1799857279","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1317279872","source":"dbSNP","start":140443764,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["CACAC","-"],"end":140443768,"feature_type":"variation","strand":1},{"id":"rs1350076813","seq_region_name":"7","clinical_significance":[],"alleles":["A","T"],"end":140443765,"strand":1,"feature_type":"variation","start":140443765,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"start":140443766,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","A"],"end":140443766,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799857352","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443768,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140443768,"clinical_significance":[],"seq_region_name":"7","id":"rs889955210"},{"end":140443773,"alleles":["ACACA","ACACATACACA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140443769,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1271841487"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799857413","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140443774,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443774},{"source":"dbSNP","start":140443779,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140443779,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs942985736"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443779,"source":"dbSNP","strand":1,"feature_type":"variation","end":140443783,"alleles":["ACACA","ACACAAACACA"],"seq_region_name":"7","id":"rs1210120408","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443782,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140443782,"clinical_significance":[],"seq_region_name":"7","id":"rs1799857480"},{"feature_type":"variation","strand":1,"end":140443784,"alleles":["C","-"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443784,"clinical_significance":[],"seq_region_name":"7","id":"rs1344840201"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799857502","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443784,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140443784},{"seq_region_name":"7","id":"rs1228861791","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["CAC","-"],"end":140443788,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443786,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140443790,"alleles":["CACAC","CACACGCACAC"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443786,"source":"dbSNP","seq_region_name":"7","id":"rs2130208509","clinical_significance":[]},{"seq_region_name":"7","id":"rs1043985040","clinical_significance":[],"alleles":["C","A"],"end":140443788,"strand":1,"feature_type":"variation","start":140443788,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"end":140443790,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140443790,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs903547904"},{"source":"dbSNP","start":140443792,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140443792,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1263459233"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443794,"source":"dbSNP","strand":1,"feature_type":"variation","end":140443794,"alleles":["C","A"],"seq_region_name":"7","id":"rs1799857620","clinical_significance":[]},{"id":"rs1245104166","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443795,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["ACA","ACAAACA"],"end":140443797},{"id":"rs1799857664","seq_region_name":"7","clinical_significance":[],"start":140443798,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140443798,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799857686","feature_type":"variation","strand":1,"alleles":["CACACACACAC","-"],"end":140443808,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443798},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443799,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["-","CACA"],"end":140443798,"seq_region_name":"7","id":"rs71991053","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443800,"feature_type":"variation","strand":1,"alleles":["CACACACAC","-"],"end":140443808,"clinical_significance":[],"seq_region_name":"7","id":"rs1799857718"},{"source":"dbSNP","start":140443801,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140443801,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799857739","seq_region_name":"7"},{"alleles":["CACACAC","-"],"end":140443808,"strand":1,"feature_type":"variation","start":140443802,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1377581836","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1311434127","end":140443809,"alleles":["CACACACG","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140443802,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443804,"source":"dbSNP","strand":1,"feature_type":"variation","end":140443804,"alleles":["C","T"],"seq_region_name":"7","id":"rs2130208569","clinical_significance":[]},{"seq_region_name":"7","id":"rs1348356122","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["CACAC","-"],"end":140443808,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443804,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["ACA","ACATACA"],"end":140443807,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443805,"clinical_significance":[],"seq_region_name":"7","id":"rs2130208576"},{"seq_region_name":"7","id":"rs1222995473","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443806,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CAC","-"],"end":140443808},{"start":140443807,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G","T"],"end":140443807,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs999161270","clinical_significance":[]},{"clinical_significance":[],"id":"rs2130208596","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","-"],"end":140443807,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443807},{"seq_region_name":"7","id":"rs1324439843","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["ACGACA","-"],"end":140443812,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443807,"source":"dbSNP"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443808,"feature_type":"variation","strand":1,"end":140443808,"alleles":["C","G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1231824099"},{"clinical_significance":[],"id":"rs1382681369","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443808,"feature_type":"variation","strand":1,"end":140443808,"alleles":["C","-"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1491491670","feature_type":"variation","strand":1,"end":140443808,"alleles":["C","CACACGC","CTC"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443808},{"source":"dbSNP","start":140443808,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140443809,"alleles":["CG","CGCG"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1554444713"},{"id":"rs1157447996","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443809,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["-","A","ACA","ACACA","ACACACA","ACACACACACA","ACACACACACACA","ACAG","AG"],"end":140443808},{"clinical_significance":[],"seq_region_name":"7","id":"rs1283878369","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443809,"feature_type":"variation","strand":1,"end":140443809,"alleles":["G","A","C","T"]},{"feature_type":"variation","strand":1,"end":140443809,"alleles":["G","-"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443809,"clinical_significance":[],"seq_region_name":"7","id":"rs1799858061"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443809,"source":"dbSNP","strand":1,"feature_type":"variation","end":140443814,"alleles":["GACAGA","GA"],"seq_region_name":"7","id":"rs1799858101","clinical_significance":[]},{"end":140443811,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140443811,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1030772748","clinical_significance":[]},{"alleles":["AGAGAGAGA","AGAGA","AGAGAGA"],"end":140443820,"strand":1,"feature_type":"variation","start":140443812,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1266444495","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443813,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["-","C"],"end":140443812,"id":"rs1799858158","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799858178","feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140443813,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443813},{"clinical_significance":[],"id":"rs896183527","seq_region_name":"7","alleles":["G","C"],"end":140443815,"feature_type":"variation","strand":1,"source":"dbSNP","start":140443815,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1799858219","clinical_significance":[],"start":140443823,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","-"],"end":140443823,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130208669","alleles":["T","C"],"end":140443823,"feature_type":"variation","strand":1,"source":"dbSNP","start":140443823,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs181809884","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140443825,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443825,"source":"dbSNP"},{"start":140443830,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140443830,"alleles":["A","G","T"],"strand":1,"feature_type":"variation","id":"rs1224855379","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443831,"feature_type":"variation","strand":1,"end":140443831,"alleles":["T","C"],"clinical_significance":[],"id":"rs1799858295","seq_region_name":"7"},{"end":140443835,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140443835,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799858315","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1048301311","source":"dbSNP","start":140443836,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140443836,"alleles":["A","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1799858367","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443838,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140443838},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443841,"feature_type":"variation","strand":1,"end":140443841,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1013428261"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799858410","source":"dbSNP","start":140443843,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140443843,"alleles":["C","G"],"feature_type":"variation","strand":1},{"alleles":["C","G","T"],"end":140443844,"feature_type":"variation","strand":1,"source":"dbSNP","start":140443844,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799858431","seq_region_name":"7"},{"start":140443848,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140443848,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1266774357","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1275519324","source":"dbSNP","start":140443850,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140443850,"feature_type":"variation","strand":1},{"end":140443855,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140443855,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1023924019","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799858524","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443863,"feature_type":"variation","strand":1,"end":140443863,"alleles":["G","C"]},{"start":140443871,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140443871,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1438831570","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1490332538","source":"dbSNP","start":140443872,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140443872,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1799858583","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443881,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140443881},{"id":"rs969245430","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443882,"source":"dbSNP","strand":1,"feature_type":"variation","end":140443882,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799858638","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443883,"feature_type":"variation","strand":1,"end":140443883,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs757898264","clinical_significance":[],"end":140443895,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140443895,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"feature_type":"variation","strand":1,"end":140443896,"alleles":["T","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443896,"clinical_significance":[],"seq_region_name":"7","id":"rs984702289"},{"feature_type":"variation","strand":1,"end":140443899,"alleles":["A","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443899,"clinical_significance":[],"seq_region_name":"7","id":"rs1799858708"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1400965007","source":"dbSNP","start":140443900,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["AGA","A"],"end":140443902,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1016107355","clinical_significance":[],"end":140443901,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140443901,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1296821618","clinical_significance":[],"strand":1,"feature_type":"variation","end":140443903,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443903,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1400640694","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140443911,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140443911},{"end":140443923,"alleles":["GGAGGAGGAGG","GGAGGAGG"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140443913,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs372244295","seq_region_name":"7"},{"alleles":["G","A"],"end":140443914,"strand":1,"feature_type":"variation","start":140443914,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","id":"rs1468960691","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140443915,"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140443915,"source":"dbSNP","seq_region_name":"7","id":"rs1799859197","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799859226","clinical_significance":[],"start":140443916,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","end":140443916,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443920,"feature_type":"variation","strand":1,"end":140443920,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799859250"},{"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443921,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140443921,"clinical_significance":[],"seq_region_name":"7","id":"rs2130208824"},{"seq_region_name":"7","id":"rs774531798","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140443922,"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140443922,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1585450144","seq_region_name":"7","consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443924,"feature_type":"variation","strand":1,"end":140443924,"alleles":["T","G"]},{"id":"rs1799859320","seq_region_name":"7","clinical_significance":[],"start":140443925,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","alleles":["G","A"],"end":140443925,"strand":1,"feature_type":"variation"},{"start":140443925,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","end":140443928,"alleles":["GGGG","GGG"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799859337","clinical_significance":[]},{"seq_region_name":"7","id":"rs532265942","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140443927,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C","T"],"end":140443927},{"seq_region_name":"7","id":"rs1799859399","clinical_significance":[],"alleles":["GTGGAG","GTGGAGTGGAG"],"end":140443933,"strand":1,"feature_type":"variation","start":140443928,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant"},{"start":140443929,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","alleles":["T","A"],"end":140443929,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130208860","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799859421","end":140443930,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140443930,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38"},{"alleles":["A","G"],"end":140443932,"feature_type":"variation","strand":1,"source":"dbSNP","start":140443932,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799859441","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs111759785","alleles":["A","C"],"end":140443935,"feature_type":"variation","strand":1,"source":"dbSNP","start":140443935,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38"},{"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443939,"feature_type":"variation","strand":1,"end":140443939,"alleles":["C","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1385503560"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140443941,"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140443941,"source":"dbSNP","seq_region_name":"7","id":"rs539211147","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799859540","clinical_significance":[],"start":140443942,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","end":140443942,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1300751633","alleles":["A","G"],"end":140443943,"feature_type":"variation","strand":1,"source":"dbSNP","start":140443943,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140443944,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","alleles":["TGG","-"],"end":140443946,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1265079299","seq_region_name":"7"},{"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443945,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140443945,"clinical_significance":[],"id":"rs1799860134","seq_region_name":"7"},{"alleles":["G","C"],"end":140443949,"feature_type":"variation","strand":1,"source":"dbSNP","start":140443949,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs918689613","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799860188","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140443950,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443950},{"seq_region_name":"7","id":"rs1364345633","clinical_significance":[],"start":140443951,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","end":140443951,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1446391663","consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443952,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140443952},{"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443956,"feature_type":"variation","strand":1,"end":140443956,"alleles":["G","A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585450169"},{"strand":1,"feature_type":"variation","end":140443957,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140443957,"source":"dbSNP","seq_region_name":"7","id":"rs1799860297","clinical_significance":[]},{"id":"rs1585450172","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140443958,"source":"dbSNP","strand":1,"feature_type":"variation","end":140443958,"alleles":["A","G"]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140443960,"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140443960,"source":"dbSNP","seq_region_name":"7","id":"rs1409894074","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140443961,"alleles":["C","T"],"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443961,"clinical_significance":[],"seq_region_name":"7","id":"rs1799860449"},{"id":"rs1220997373","seq_region_name":"7","clinical_significance":[],"alleles":["C","G"],"end":140443966,"strand":1,"feature_type":"variation","start":140443966,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140443970,"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140443970,"source":"dbSNP","seq_region_name":"7","id":"rs955679662","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140443975,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140443975,"seq_region_name":"7","id":"rs569062881","clinical_significance":[]},{"start":140443977,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","alleles":["G","A"],"end":140443977,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1282865935","clinical_significance":[]},{"seq_region_name":"7","id":"rs986902700","clinical_significance":[],"start":140443984,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","end":140443984,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1799860589","seq_region_name":"7","source":"dbSNP","start":140443988,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140443988,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140443989,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140443989,"source":"dbSNP","seq_region_name":"7","id":"rs1799860613","clinical_significance":[]},{"seq_region_name":"7","id":"rs968865304","clinical_significance":[],"start":140443990,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","end":140443990,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"start":140443993,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","end":140443993,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1276731116","clinical_significance":[]},{"seq_region_name":"7","id":"rs1430579647","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140443994,"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140443994,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1333879620","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140443996,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140443996},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140444002,"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140444002,"source":"dbSNP","id":"rs1799860734","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130208990","source":"dbSNP","start":140444003,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","end":140444003,"alleles":["T","C"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140444004,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140444004,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130208994"},{"alleles":["G","C"],"end":140444005,"strand":1,"feature_type":"variation","start":140444005,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","seq_region_name":"7","id":"rs1799860754","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585450193","consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444014,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140444014},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130209005","consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444016,"feature_type":"variation","strand":1,"alleles":["GGCCCGGCCTG","GGCCCGGCCTGGGCCCGGCCTG"],"end":140444026},{"seq_region_name":"7","id":"rs1415678377","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140444020,"source":"dbSNP","strand":1,"feature_type":"variation","end":140444020,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs759977489","consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444021,"feature_type":"variation","strand":1,"end":140444021,"alleles":["G","A","C"]},{"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444025,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140444025,"clinical_significance":[],"seq_region_name":"7","id":"rs942830940"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1477947207","consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444026,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140444026},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799860875","alleles":["T","C"],"end":140444029,"feature_type":"variation","strand":1,"source":"dbSNP","start":140444029,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1799860894","clinical_significance":[],"start":140444030,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","end":140444033,"alleles":["ACAC","AC"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1799860915","clinical_significance":[],"end":140444031,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140444031,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799860931","feature_type":"variation","strand":1,"alleles":["C","-"],"end":140444031,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444031},{"seq_region_name":"7","id":"rs1044013714","clinical_significance":[],"alleles":["T","C"],"end":140444034,"strand":1,"feature_type":"variation","start":140444034,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant"},{"seq_region_name":"7","id":"rs1184587869","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140444036,"source":"dbSNP","strand":1,"feature_type":"variation","end":140444036,"alleles":["T","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799861008","source":"dbSNP","start":140444036,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","end":140444040,"alleles":["TCTCT","TCT"],"feature_type":"variation","strand":1},{"alleles":["C","G","T"],"end":140444039,"strand":1,"feature_type":"variation","start":140444039,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","seq_region_name":"7","id":"rs1799861025","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799861046","clinical_significance":[],"start":140444044,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","alleles":["A","G"],"end":140444044,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1474990352","clinical_significance":[],"end":140444046,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140444046,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant"},{"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140444049,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140444049,"seq_region_name":"7","id":"rs1284527709","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs956602613","feature_type":"variation","strand":1,"end":140444058,"alleles":["C","T"],"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444058},{"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140444066,"source":"dbSNP","strand":1,"feature_type":"variation","end":140444066,"alleles":["C","T"],"seq_region_name":"7","id":"rs115862359","clinical_significance":[]},{"seq_region_name":"7","id":"rs1262589900","clinical_significance":[],"end":140444076,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140444076,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant"},{"seq_region_name":"7","id":"rs1799861200","clinical_significance":[],"start":140444077,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","end":140444077,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"end":140444078,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140444078,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130209090"},{"alleles":["T","C"],"end":140444082,"strand":1,"feature_type":"variation","start":140444082,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","seq_region_name":"7","id":"rs917684139","clinical_significance":[]},{"seq_region_name":"7","id":"rs1289845290","clinical_significance":[],"start":140444083,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","end":140444083,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"end":140444087,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140444087,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","seq_region_name":"7","id":"rs1799861278","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1293766141","source":"dbSNP","start":140444088,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140444088,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs934985374","clinical_significance":[],"start":140444090,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","alleles":["G","A"],"end":140444090,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140444091,"source":"dbSNP","strand":1,"feature_type":"variation","end":140444091,"alleles":["C","A"],"seq_region_name":"7","id":"rs980581984","clinical_significance":[]},{"start":140444096,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","alleles":["G","A"],"end":140444096,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585450215","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140444097,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140444097,"source":"dbSNP","seq_region_name":"7","id":"rs1286454309","clinical_significance":[]},{"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444099,"feature_type":"variation","strand":1,"end":140444099,"alleles":["A","C"],"clinical_significance":[],"id":"rs1446481254","seq_region_name":"7"},{"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444104,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140444104,"clinical_significance":[],"seq_region_name":"7","id":"rs1799861448"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1379857106","feature_type":"variation","strand":1,"end":140444113,"alleles":["CTC","C"],"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444111},{"start":140444117,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","end":140444117,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1335536854","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140444120,"alleles":["A","G"],"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444120,"clinical_significance":[],"seq_region_name":"7","id":"rs1799861500"},{"seq_region_name":"7","id":"rs1358898747","clinical_significance":[],"alleles":["C","T"],"end":140444126,"strand":1,"feature_type":"variation","start":140444126,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs74914081","source":"dbSNP","start":140444127,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","end":140444127,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799861609","source":"dbSNP","start":140444129,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140444129,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140444134,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140444134,"id":"rs2130209169","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444136,"feature_type":"variation","strand":1,"end":140444136,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130209174"},{"source":"dbSNP","start":140444137,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","end":140444137,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs896145604","seq_region_name":"7"},{"start":140444138,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","alleles":["T","G"],"end":140444138,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1253342566","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140444140,"source":"dbSNP","strand":1,"feature_type":"variation","end":140444140,"alleles":["G","T"],"id":"rs1799861694","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799861711","seq_region_name":"7","feature_type":"variation","strand":1,"end":140444145,"alleles":["ATA","A"],"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444143},{"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444144,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140444144,"clinical_significance":[],"seq_region_name":"7","id":"rs1799861735"},{"start":140444147,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","end":140444147,"alleles":["A","G"],"strand":1,"feature_type":"variation","id":"rs1048815982","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1409154809","seq_region_name":"7","alleles":["C","A"],"end":140444148,"feature_type":"variation","strand":1,"source":"dbSNP","start":140444148,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140444149,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444149,"clinical_significance":[],"seq_region_name":"7","id":"rs1799861778"},{"source":"dbSNP","start":140444150,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","end":140444150,"alleles":["C","A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799861805","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1414269221","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140444151,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140444151},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799861833","end":140444153,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140444153,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38"},{"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444157,"feature_type":"variation","strand":1,"end":140444157,"alleles":["G","A"],"clinical_significance":[],"id":"rs1799861858","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799861884","clinical_significance":[],"start":140444161,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","alleles":["C","T"],"end":140444161,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs566940905","end":140444164,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140444164,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38"},{"start":140444166,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","alleles":["G","C"],"end":140444166,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1442732376","clinical_significance":[]},{"alleles":["G","T"],"end":140444167,"strand":1,"feature_type":"variation","start":140444167,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","seq_region_name":"7","id":"rs1799862026","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140444169,"alleles":["GTG","G"],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140444167,"source":"dbSNP","seq_region_name":"7","id":"rs1799862051","clinical_significance":[]},{"clinical_significance":[],"id":"rs1044801220","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140444168,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444168},{"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444175,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140444175,"clinical_significance":[],"seq_region_name":"7","id":"rs905038667"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140444176,"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140444176,"source":"dbSNP","seq_region_name":"7","id":"rs1799862129","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799862152","clinical_significance":[],"start":140444178,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","alleles":["T","C","G"],"end":140444178,"strand":1,"feature_type":"variation"},{"end":140444179,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140444179,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","seq_region_name":"7","id":"rs1179310304","clinical_significance":[]},{"id":"rs1459174380","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140444180,"strand":1,"feature_type":"variation","start":140444180,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant"},{"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444181,"feature_type":"variation","strand":1,"end":140444181,"alleles":["A","C"],"clinical_significance":[],"id":"rs1799862225","seq_region_name":"7"},{"id":"rs534317003","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140444183,"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140444183,"source":"dbSNP"},{"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444184,"feature_type":"variation","strand":1,"end":140444184,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs144294747"},{"source":"dbSNP","start":140444185,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140444185,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799862293","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140444186,"source":"dbSNP","strand":1,"feature_type":"variation","end":140444186,"alleles":["G","A","C"],"id":"rs1016138356","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799862313","consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444188,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140444188},{"seq_region_name":"7","id":"rs901264518","clinical_significance":[],"alleles":["G","C","T"],"end":140444196,"strand":1,"feature_type":"variation","start":140444196,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant"},{"alleles":["T","A"],"end":140444198,"feature_type":"variation","strand":1,"source":"dbSNP","start":140444198,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1244057463"},{"assembly_name":"GRCh38","consequence_type":"TF_binding_site_variant","start":140444201,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C","T"],"end":140444201,"id":"rs1446097709","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1244370971","clinical_significance":[],"alleles":["G","A"],"end":140444203,"strand":1,"feature_type":"variation","start":140444203,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"TF_binding_site_variant"},{"seq_region_name":"7","id":"rs961902867","clinical_significance":[],"strand":1,"feature_type":"variation","end":140444204,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"TF_binding_site_variant","start":140444204,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1310695348","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140444208,"assembly_name":"GRCh38","consequence_type":"TF_binding_site_variant","start":140444208,"source":"dbSNP"},{"alleles":["G","GG"],"end":140444210,"feature_type":"variation","strand":1,"source":"dbSNP","start":140444210,"consequence_type":"TF_binding_site_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799862481"},{"clinical_significance":[],"id":"rs1799862500","seq_region_name":"7","end":140444214,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140444214,"consequence_type":"TF_binding_site_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1161350835","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140444216,"assembly_name":"GRCh38","consequence_type":"TF_binding_site_variant","start":140444216,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799862551","clinical_significance":[],"strand":1,"feature_type":"variation","end":140444217,"alleles":["GG","G"],"assembly_name":"GRCh38","consequence_type":"TF_binding_site_variant","start":140444216,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1446849065","source":"dbSNP","start":140444217,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","end":140444217,"alleles":["G","C"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140444219,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140444219,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs78465098"},{"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444230,"feature_type":"variation","strand":1,"end":140444230,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1296084452"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1026107521","consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444231,"feature_type":"variation","strand":1,"end":140444231,"alleles":["G","A","T"]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140444233,"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140444233,"source":"dbSNP","id":"rs1799862668","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799862695","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140444235,"source":"dbSNP","strand":1,"feature_type":"variation","end":140444235,"alleles":["C","T"]},{"start":140444237,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","end":140444237,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs761039412","clinical_significance":[]},{"source":"dbSNP","start":140444238,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140444238,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs987321369","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140444241,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140444241,"source":"dbSNP","seq_region_name":"7","id":"rs1799864550","clinical_significance":[]},{"seq_region_name":"7","id":"rs538244596","clinical_significance":[],"start":140444244,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","alleles":["G","A"],"end":140444244,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140444246,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140444246,"id":"rs146594412","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1422565643","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140444248,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140444248},{"clinical_significance":[],"seq_region_name":"7","id":"rs1384499447","alleles":["G","C","T"],"end":140444252,"feature_type":"variation","strand":1,"source":"dbSNP","start":140444252,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1159248007","clinical_significance":[],"alleles":["G","A","C"],"end":140444254,"strand":1,"feature_type":"variation","start":140444254,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799864695","alleles":["A","T"],"end":140444256,"feature_type":"variation","strand":1,"source":"dbSNP","start":140444256,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs2130209415","clinical_significance":[],"strand":1,"feature_type":"variation","end":140444257,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140444257,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1441606239","seq_region_name":"7","source":"dbSNP","start":140444260,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","end":140444260,"alleles":["A","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1248526610","clinical_significance":[],"strand":1,"feature_type":"variation","end":140444262,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140444262,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140444264,"alleles":["T","A"],"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444264,"clinical_significance":[],"seq_region_name":"7","id":"rs1176765363"},{"start":140444265,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","alleles":["C","T"],"end":140444265,"strand":1,"feature_type":"variation","id":"rs560210033","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140444266,"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140444266,"source":"dbSNP","seq_region_name":"7","id":"rs1799864786","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1248772211","alleles":["A","G"],"end":140444270,"feature_type":"variation","strand":1,"source":"dbSNP","start":140444270,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38"},{"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444275,"feature_type":"variation","strand":1,"end":140444276,"alleles":["AA","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1220692658"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1359229415","source":"dbSNP","start":140444276,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","end":140444276,"alleles":["A","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1799864885","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140444286,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140444286},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799864911","consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444289,"feature_type":"variation","strand":1,"end":140444289,"alleles":["T","C"]},{"source":"dbSNP","start":140444290,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","end":140444290,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799864936","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140444294,"alleles":["C","T"],"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444294,"clinical_significance":[],"id":"rs964223703","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140444297,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444297,"clinical_significance":[],"id":"rs1390680012","seq_region_name":"7"},{"seq_region_name":"7","id":"rs187251768","clinical_significance":[],"end":140444298,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140444298,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant"},{"clinical_significance":[],"id":"rs1799865079","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140444303,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444303},{"clinical_significance":[],"seq_region_name":"7","id":"rs1318144264","consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444307,"feature_type":"variation","strand":1,"end":140444307,"alleles":["C","T"]},{"start":140444310,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","alleles":["A","C"],"end":140444310,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585450307","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140444311,"alleles":["C","T"],"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444311,"clinical_significance":[],"seq_region_name":"7","id":"rs1384791982"},{"id":"rs141375044","seq_region_name":"7","clinical_significance":[],"alleles":["A","G"],"end":140444312,"strand":1,"feature_type":"variation","start":140444312,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant"},{"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444313,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140444313,"clinical_significance":[],"seq_region_name":"7","id":"rs1367838225"},{"start":140444314,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","alleles":["CTGTAATC","C"],"end":140444321,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1304622096","clinical_significance":[]},{"end":140444316,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140444316,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","seq_region_name":"7","id":"rs1799865249","clinical_significance":[]},{"start":140444316,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","end":140444316,"alleles":["G","-"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799865269","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799865289","clinical_significance":[],"end":140444319,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140444319,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1402865516","feature_type":"variation","strand":1,"end":140444321,"alleles":["C","A"],"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444321},{"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444322,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140444322,"clinical_significance":[],"seq_region_name":"7","id":"rs1799865332"},{"clinical_significance":[],"seq_region_name":"7","id":"rs935602662","consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444323,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140444323},{"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140444324,"source":"dbSNP","strand":1,"feature_type":"variation","end":140444324,"alleles":["A","T"],"id":"rs2130209562","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1052697905","alleles":["T","C"],"end":140444329,"feature_type":"variation","strand":1,"source":"dbSNP","start":140444329,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38"},{"id":"rs1382278432","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140444330,"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140444330,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs190436277","feature_type":"variation","strand":1,"alleles":["T","A"],"end":140444331,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444331},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140444332,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444332,"clinical_significance":[],"id":"rs1228271320","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140444335,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140444335,"seq_region_name":"7","id":"rs917596976","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140444339,"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140444339,"source":"dbSNP","seq_region_name":"7","id":"rs2130209600","clinical_significance":[]},{"end":140444340,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140444340,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","seq_region_name":"7","id":"rs949067990","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140444344,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444344,"source":"dbSNP","seq_region_name":"7","id":"rs1045236202","clinical_significance":[]},{"end":140444345,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140444345,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799865570","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799865587","clinical_significance":[],"start":140444348,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140444348,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140444349,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444349,"source":"dbSNP","seq_region_name":"7","id":"rs1264289074","clinical_significance":[]},{"id":"rs1158506576","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444352,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140444352},{"source":"dbSNP","start":140444354,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140444354,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1433895858"},{"seq_region_name":"7","id":"rs2130209642","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["CGAGG","-"],"end":140444359,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444355,"source":"dbSNP"},{"start":140444357,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140444357,"alleles":["A","C"],"strand":1,"feature_type":"variation","id":"rs1427493740","seq_region_name":"7","clinical_significance":[]},{"start":140444360,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140444360,"alleles":["T","G"],"strand":1,"feature_type":"variation","id":"rs947574800","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140444365,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140444365,"alleles":["A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799865713"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444366,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140444366,"clinical_significance":[],"seq_region_name":"7","id":"rs904913489"},{"seq_region_name":"7","id":"rs1264370221","clinical_significance":[],"strand":1,"feature_type":"variation","end":140444369,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444369,"source":"dbSNP"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444373,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140444373,"clinical_significance":[],"id":"rs1585450362","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140444374,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444374,"clinical_significance":[],"seq_region_name":"7","id":"rs1182104699"},{"id":"rs1219374753","seq_region_name":"7","clinical_significance":[],"end":140444378,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140444378,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"id":"rs1799865840","seq_region_name":"7","clinical_significance":[],"start":140444383,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140444383,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444386,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140444386,"seq_region_name":"7","id":"rs1799865855","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444390,"source":"dbSNP","strand":1,"feature_type":"variation","end":140444390,"alleles":["G","A"],"id":"rs1799865877","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444392,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140444392,"seq_region_name":"7","id":"rs988215364","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["CCCCC","CCCCCC"],"end":140444401,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444397,"source":"dbSNP","seq_region_name":"7","id":"rs1799865926","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444400,"feature_type":"variation","strand":1,"end":140444400,"alleles":["C","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs867239385"},{"end":140444401,"alleles":["C","A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140444401,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs867701906","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1585450380","clinical_significance":[],"end":140444403,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140444403,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"start":140444404,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140444404,"alleles":["T","C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799866020","clinical_significance":[]},{"end":140444408,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140444408,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1428696962","seq_region_name":"7","clinical_significance":[]},{"start":140444415,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140444415,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799866071","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140444417,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444417,"clinical_significance":[],"seq_region_name":"7","id":"rs1194697878"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444417,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","-"],"end":140444417,"seq_region_name":"7","id":"rs1799866123","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799866148","feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140444418,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444418},{"clinical_significance":[],"seq_region_name":"7","id":"rs1312333290","source":"dbSNP","start":140444418,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["AAAA","AAA"],"end":140444421,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs762930134","feature_type":"variation","strand":1,"end":140444422,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444422},{"start":140444423,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140444423,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130209777","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444428,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140444428,"clinical_significance":[],"seq_region_name":"7","id":"rs746683720"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799866254","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444429,"feature_type":"variation","strand":1,"end":140444429,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs112964326","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140444432,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444432,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140444433,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444433,"clinical_significance":[],"seq_region_name":"7","id":"rs1799866321"},{"seq_region_name":"7","id":"rs1563081453","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444434,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140444434},{"seq_region_name":"7","id":"rs539978187","clinical_significance":[],"start":140444435,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140444435,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs897662167","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444437,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140444437},{"seq_region_name":"7","id":"rs993401799","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444442,"source":"dbSNP","strand":1,"feature_type":"variation","end":140444442,"alleles":["A","G"]},{"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140444444,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444444,"source":"dbSNP","id":"rs180688809","seq_region_name":"7","clinical_significance":[]},{"end":140444445,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140444445,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs539189168","clinical_significance":[]},{"seq_region_name":"7","id":"rs908475425","clinical_significance":[],"start":140444452,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140444452,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1174478490","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140444454,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444454,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1382926653","clinical_significance":[],"strand":1,"feature_type":"variation","end":140444455,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444455,"source":"dbSNP"},{"end":140444461,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140444461,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130209862"},{"start":140444462,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140444462,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799866588","clinical_significance":[]},{"end":140444463,"alleles":["T","A","G"],"strand":1,"feature_type":"variation","start":140444463,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799866637","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1480237773","source":"dbSNP","start":140444464,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140444464,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1799866694","clinical_significance":[],"start":140444465,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140444465,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"alleles":["G","A"],"end":140444469,"feature_type":"variation","strand":1,"source":"dbSNP","start":140444469,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130209888"},{"id":"rs1424721774","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444470,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140444470},{"clinical_significance":[],"seq_region_name":"7","id":"rs1196265891","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140444471,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444471},{"source":"dbSNP","start":140444477,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140444477,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1585450448","seq_region_name":"7"},{"source":"dbSNP","start":140444480,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140444480,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799866785"},{"id":"rs1297835473","seq_region_name":"7","clinical_significance":[],"start":140444486,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","A","G","T"],"end":140444486,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140444492,"alleles":["G","A","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444492,"clinical_significance":[],"seq_region_name":"7","id":"rs939926329"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444493,"source":"dbSNP","strand":1,"feature_type":"variation","end":140444493,"alleles":["A","G"],"seq_region_name":"7","id":"rs1008202762","clinical_significance":[]},{"end":140444494,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140444494,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1324821878","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799866921","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444496,"feature_type":"variation","strand":1,"end":140444496,"alleles":["C","T"]},{"alleles":["G","C"],"end":140444497,"feature_type":"variation","strand":1,"source":"dbSNP","start":140444497,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1264463989"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1226784308","alleles":["GGG","GG"],"end":140444499,"feature_type":"variation","strand":1,"source":"dbSNP","start":140444497,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1799866993","clinical_significance":[],"alleles":["G","A"],"end":140444505,"strand":1,"feature_type":"variation","start":140444505,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"id":"rs1284533636","seq_region_name":"7","end":140444508,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140444508,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444509,"source":"dbSNP","strand":1,"feature_type":"variation","end":140444509,"alleles":["T","A"],"seq_region_name":"7","id":"rs1018776183","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444512,"feature_type":"variation","strand":1,"end":140444512,"alleles":["T","C"],"clinical_significance":[],"id":"rs1799867076","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140444513,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444513,"clinical_significance":[],"id":"rs2130209971","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140444514,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444514,"source":"dbSNP","seq_region_name":"7","id":"rs1201342594","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799867124","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140444517,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444517},{"source":"dbSNP","start":140444518,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140444518,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1322428589"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444519,"source":"dbSNP","strand":1,"feature_type":"variation","end":140444519,"alleles":["T","C"],"seq_region_name":"7","id":"rs1799867167","clinical_significance":[]},{"end":140444521,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140444521,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs964089144"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444523,"feature_type":"variation","strand":1,"end":140444523,"alleles":["G","C"],"clinical_significance":[],"id":"rs1040971053","seq_region_name":"7"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444526,"feature_type":"variation","strand":1,"end":140444526,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799867411"},{"feature_type":"variation","strand":1,"end":140444527,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444527,"clinical_significance":[],"seq_region_name":"7","id":"rs1799867435"},{"seq_region_name":"7","id":"rs1262833582","clinical_significance":[],"start":140444528,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140444528,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444529,"source":"dbSNP","strand":1,"feature_type":"variation","end":140444529,"alleles":["G","A","T"],"id":"rs979503195","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","A","T"],"end":140444530,"strand":1,"feature_type":"variation","start":140444530,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1206583574","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799868317","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444533,"feature_type":"variation","strand":1,"end":140444533,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1032550648","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140444537,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444537},{"alleles":["C","T"],"end":140444538,"feature_type":"variation","strand":1,"source":"dbSNP","start":140444538,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1259224552"},{"seq_region_name":"7","id":"rs139036014","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444541,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140444541},{"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140444544,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444544,"source":"dbSNP","seq_region_name":"7","id":"rs1427448111","clinical_significance":[]},{"id":"rs1799868432","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444545,"source":"dbSNP","strand":1,"feature_type":"variation","end":140444545,"alleles":["C","G"]},{"source":"dbSNP","start":140444549,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140444549,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130210068"},{"start":140444551,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140444551,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1199482307","clinical_significance":[]},{"clinical_significance":[],"id":"rs1334812974","seq_region_name":"7","alleles":["C","A"],"end":140444553,"feature_type":"variation","strand":1,"source":"dbSNP","start":140444553,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1401258974","seq_region_name":"7","source":"dbSNP","start":140444558,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140444558,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140444558,"alleles":["C","-"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444558,"source":"dbSNP","id":"rs1469395846","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140444562,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444562,"source":"dbSNP","seq_region_name":"7","id":"rs543889056","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444563,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140444563,"clinical_significance":[],"seq_region_name":"7","id":"rs988827472"},{"clinical_significance":[],"seq_region_name":"7","id":"rs918152744","source":"dbSNP","start":140444565,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140444565,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs932637207","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444567,"feature_type":"variation","strand":1,"end":140444567,"alleles":["A","G"]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444568,"source":"dbSNP","strand":1,"feature_type":"variation","end":140444568,"alleles":["T","A"],"id":"rs113751584","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1447008841","source":"dbSNP","start":140444569,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140444569,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1585450532","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["AAAAA","AAAA"],"end":140444576,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444572,"source":"dbSNP"},{"alleles":["A","G"],"end":140444573,"feature_type":"variation","strand":1,"source":"dbSNP","start":140444573,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1181180721"},{"clinical_significance":[],"id":"rs904573081","seq_region_name":"7","source":"dbSNP","start":140444573,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140444591,"alleles":["AAAACAAAACAAAACAAAA","AAAACAAAACAAAA","AAAACAAAACAAAACAAAACAAAA"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1799868810","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444576,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140444576},{"id":"rs1460524342","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140444580,"alleles":["A","C","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444580,"source":"dbSNP"},{"end":140444581,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140444581,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799868925","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs980430408","source":"dbSNP","start":140444583,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140444583,"alleles":["A","C"],"feature_type":"variation","strand":1},{"start":140444583,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140444586,"alleles":["AAAA","AAAAA"],"strand":1,"feature_type":"variation","id":"rs2130210158","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","G"],"end":140444584,"strand":1,"feature_type":"variation","start":140444584,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1197249233","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799868984","clinical_significance":[],"strand":1,"feature_type":"variation","end":140444586,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444586,"source":"dbSNP"},{"source":"dbSNP","start":140444587,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140444587,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs926284469"},{"seq_region_name":"7","id":"rs1799869035","clinical_significance":[],"alleles":["A","C"],"end":140444592,"strand":1,"feature_type":"variation","start":140444592,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"end":140444594,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140444594,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1250558790"},{"seq_region_name":"7","id":"rs185264413","clinical_significance":[],"start":140444595,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","C","G"],"end":140444595,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1345508468","seq_region_name":"7","end":140444600,"alleles":["AGTCAG","AG"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140444595,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1312902415","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444596,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C","T"],"end":140444596},{"end":140444600,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140444600,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1451993683"},{"feature_type":"variation","strand":1,"end":140444601,"alleles":["G","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444601,"clinical_significance":[],"seq_region_name":"7","id":"rs1799869207"},{"feature_type":"variation","strand":1,"end":140444605,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444605,"clinical_significance":[],"seq_region_name":"7","id":"rs1037396937"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444606,"feature_type":"variation","strand":1,"end":140444606,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1290925408"},{"source":"dbSNP","start":140444610,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140444610,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs897694779"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799869283","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444611,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140444611},{"start":140444613,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140444613,"alleles":["G","C"],"strand":1,"feature_type":"variation","id":"rs929128460","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","A","G","T"],"end":140444614,"strand":1,"feature_type":"variation","start":140444614,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs113367286","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140444615,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444615,"source":"dbSNP","seq_region_name":"7","id":"rs1389904850","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585450583","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444616,"feature_type":"variation","strand":1,"end":140444616,"alleles":["C","G"]},{"clinical_significance":[],"id":"rs1396165633","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444627,"feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140444627},{"clinical_significance":[],"seq_region_name":"7","id":"rs1164230364","feature_type":"variation","strand":1,"alleles":["A","T"],"end":140444628,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444628},{"alleles":["C","T"],"end":140444629,"feature_type":"variation","strand":1,"source":"dbSNP","start":140444629,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130210272"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444632,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140444632,"clinical_significance":[],"id":"rs924820153","seq_region_name":"7"},{"end":140444633,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140444633,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799869500","clinical_significance":[]},{"seq_region_name":"7","id":"rs1383901383","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140444634,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444634,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1163570993","source":"dbSNP","start":140444646,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140444646,"alleles":["G","A"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140444647,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444647,"clinical_significance":[],"seq_region_name":"7","id":"rs1799869553"},{"seq_region_name":"7","id":"rs890336683","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140444652,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444652,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1443472783","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444656,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140444656},{"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140444657,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444657,"clinical_significance":[],"seq_region_name":"7","id":"rs1363878481"},{"seq_region_name":"7","id":"rs1799869641","clinical_significance":[],"strand":1,"feature_type":"variation","end":140444661,"alleles":["G","GG"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444661,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140444662,"alleles":["A","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444662,"clinical_significance":[],"id":"rs531527796","seq_region_name":"7"},{"clinical_significance":[],"id":"rs566352028","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444665,"feature_type":"variation","strand":1,"end":140444665,"alleles":["C","T"]},{"clinical_significance":[],"id":"rs548345134","seq_region_name":"7","end":140444666,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140444666,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"end":140444671,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140444671,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1301168769","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444673,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140444673,"id":"rs1490797002","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","C"],"end":140444675,"feature_type":"variation","strand":1,"source":"dbSNP","start":140444675,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130210346"},{"start":140444678,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140444678,"strand":1,"feature_type":"variation","id":"rs899830685","seq_region_name":"7","clinical_significance":[]},{"id":"rs1241583879","seq_region_name":"7","clinical_significance":[],"start":140444680,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140444680,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1245159467","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444682,"feature_type":"variation","strand":1,"end":140444682,"alleles":["A","C"]},{"end":140444684,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140444684,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1799869870","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140444685,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444685,"source":"dbSNP","seq_region_name":"7","id":"rs1799869893","clinical_significance":[]},{"alleles":["G","A"],"end":140444687,"strand":1,"feature_type":"variation","start":140444687,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1799869909","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140444690,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444690,"clinical_significance":[],"seq_region_name":"7","id":"rs1799869931"},{"start":140444692,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140444692,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130210388","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799869947","clinical_significance":[],"alleles":["T","C"],"end":140444694,"strand":1,"feature_type":"variation","start":140444694,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"id":"rs1799869968","seq_region_name":"7","source":"dbSNP","start":140444706,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G","T"],"end":140444706,"feature_type":"variation","strand":1},{"start":140444710,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140444710,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs952474635","clinical_significance":[]},{"id":"rs1799870015","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140444712,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444712,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1258637776","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444715,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140444715},{"end":140444716,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140444716,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1000973430"},{"seq_region_name":"7","id":"rs1222623328","clinical_significance":[],"end":140444719,"alleles":["C","A","G","T"],"strand":1,"feature_type":"variation","start":140444719,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"end":140444720,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140444720,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1799870081","seq_region_name":"7","clinical_significance":[]},{"id":"rs1270333453","seq_region_name":"7","clinical_significance":[],"start":140444723,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","AA"],"end":140444723,"strand":1,"feature_type":"variation"},{"id":"rs1799870113","seq_region_name":"7","clinical_significance":[],"end":140444724,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140444724,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1489843716","clinical_significance":[],"end":140444728,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140444728,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444730,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140444730,"clinical_significance":[],"id":"rs1198680156","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140444731,"alleles":["A","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444731,"clinical_significance":[],"seq_region_name":"7","id":"rs1335366688"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1032414968","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140444732,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444732},{"start":140444735,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140444735,"alleles":["T","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799870190","clinical_significance":[]},{"source":"dbSNP","start":140444735,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140444735,"alleles":["T","TT"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799870218"},{"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140444737,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444737,"clinical_significance":[],"seq_region_name":"7","id":"rs956870838"},{"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140444742,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444742,"clinical_significance":[],"seq_region_name":"7","id":"rs199704505"},{"end":140444750,"alleles":["AATAATAA","AATAATAAAATAATAATAATAATAATAATAATAA"],"strand":1,"feature_type":"variation","start":140444743,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799870269","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799870291","feature_type":"variation","strand":1,"alleles":["AATAATAATAAT","AATAATAATAATTAATAATAATAATAATAATAATAAT"],"end":140444754,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444743},{"end":140444756,"alleles":["AATAATAATAATAA","AATAATAATAATAAATAATAATAATAATAATAATAATAA"],"strand":1,"feature_type":"variation","start":140444743,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1554444795","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799870331","source":"dbSNP","start":140444743,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["AATAATAATAATAATAA","AATAATAATAATAATAACAATAATAATAATAATAATAATAATAATAATAA","AATAATAATAATAATAACAATAATAATAATAATAATAATAATAATAATAATAA"],"end":140444759,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140444743,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["AATAATAATAATAATAATAATAAT","AATAATAATAATAAT","AATAATAATAATAATAAT","AATAATAATAATAATAATAAT","AATAATAATAATAATAATAATAATAAT","AATAATAATAATAATAATAATAATAATAAT","AATAATAATAATAATAATAATAATAATAATAAT","AATAATAATAATAATAATAATAATAATAATAATAAT","AATAATAATAATAATAATAATAATAATAATAATAATAAT","AATAATAATAATAATAATAATAATAATAATAATAATAATAAT","AATAATAATAATAATAATAATAATAATAATAATAATAATAATAAT","AATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAAT","AATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAAT","AATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAAT","AATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAAT"],"end":140444766,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs774647933"},{"feature_type":"variation","strand":1,"end":140444747,"alleles":["A","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444747,"clinical_significance":[],"seq_region_name":"7","id":"rs550148690"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140444749,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444749,"clinical_significance":[],"seq_region_name":"7","id":"rs1025657100"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444751,"feature_type":"variation","strand":1,"alleles":["TAAT","TAATTAAT"],"end":140444754,"clinical_significance":[],"seq_region_name":"7","id":"rs1799870580"},{"source":"dbSNP","start":140444752,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140444752,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799870597"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444752,"source":"dbSNP","strand":1,"feature_type":"variation","end":140444766,"alleles":["AATAATAATAATAAT","AATAATAATAATAATAAAAATAATAATAATAAT","AATAATAATAATAATAATAACAATAATAATAATAAT"],"seq_region_name":"7","id":"rs1420699195","clinical_significance":[]},{"source":"dbSNP","start":140444755,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140444756,"alleles":["AA","AAA"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799870649"},{"clinical_significance":[],"id":"rs1799870672","seq_region_name":"7","source":"dbSNP","start":140444760,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140444760,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140444761,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140444761,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585450682"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1203443411","source":"dbSNP","start":140444763,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140444763,"alleles":["T","A","C"],"feature_type":"variation","strand":1},{"end":140444764,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140444764,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1225585015","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1350119311","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444765,"feature_type":"variation","strand":1,"end":140444766,"alleles":["AT","ATAATAATAATAATAATAATAATAATGAT","ATAATAATAATAATAATAATAATGAT","ATAATAATAATAATAATAATGAT","ATAATAATAATAATAATGAT","ATAATGAT"]},{"strand":1,"feature_type":"variation","end":140444769,"alleles":["ATGAT","ATGATGAT"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444765,"source":"dbSNP","seq_region_name":"7","id":"rs1799870805","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs62490430","source":"dbSNP","start":140444767,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140444767,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799870868","feature_type":"variation","strand":1,"end":140444774,"alleles":["AAAGA","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444770},{"end":140444774,"alleles":["AAGA","A"],"strand":1,"feature_type":"variation","start":140444771,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799870896","clinical_significance":[]},{"id":"rs78025113","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140444772,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444772,"source":"dbSNP"},{"seq_region_name":"7","id":"rs74861204","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140444773,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444773,"source":"dbSNP"},{"source":"dbSNP","start":140444774,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140444774,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799870987"},{"strand":1,"feature_type":"variation","alleles":["ATAATAATA","ATAATA"],"end":140444782,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444774,"source":"dbSNP","id":"rs1799871009","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799871059","clinical_significance":[],"start":140444775,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140444775,"strand":1,"feature_type":"variation"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444776,"feature_type":"variation","strand":1,"end":140444776,"alleles":["A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1347445202"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444778,"feature_type":"variation","strand":1,"end":140444778,"alleles":["T","A"],"clinical_significance":[],"id":"rs1316917585","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140444781,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444781,"source":"dbSNP","seq_region_name":"7","id":"rs1799871120","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444783,"feature_type":"variation","strand":1,"end":140444783,"alleles":["G","A","C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs976707004"},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140444785,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444785,"source":"dbSNP","id":"rs1176634176","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799871211","feature_type":"variation","strand":1,"end":140444786,"alleles":["T","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444786},{"end":140444789,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140444789,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs565015000"},{"strand":1,"feature_type":"variation","end":140444790,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444790,"source":"dbSNP","id":"rs1799871280","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444794,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140444794,"seq_region_name":"7","id":"rs527778184","clinical_significance":[]},{"end":140444797,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140444797,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs926317036"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1198381856","feature_type":"variation","strand":1,"end":140444799,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444799},{"alleles":["A","G"],"end":140444802,"strand":1,"feature_type":"variation","start":140444802,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1475647104","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140444803,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444803,"source":"dbSNP","seq_region_name":"7","id":"rs115371640","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444813,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140444813,"seq_region_name":"7","id":"rs1799871433","clinical_significance":[]},{"seq_region_name":"7","id":"rs1403174893","clinical_significance":[],"start":140444815,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140444815,"strand":1,"feature_type":"variation"},{"id":"rs1293496778","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444816,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140444816},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799871580","source":"dbSNP","start":140444827,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140444827,"alleles":["G","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs973142365","clinical_significance":[],"strand":1,"feature_type":"variation","end":140444828,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444828,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1374661437","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444829,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140444829},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140444830,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444830,"clinical_significance":[],"seq_region_name":"7","id":"rs143012225"},{"clinical_significance":[],"seq_region_name":"7","id":"rs929132508","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444831,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140444831},{"feature_type":"variation","strand":1,"alleles":["GGGGGG","GGGGG","GGGGGGG"],"end":140444836,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444831,"clinical_significance":[],"id":"rs200294319","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799871777","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140444832,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444832,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1219624761","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444833,"feature_type":"variation","strand":1,"end":140444833,"alleles":["G","A"]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444834,"source":"dbSNP","strand":1,"feature_type":"variation","end":140444834,"alleles":["G","A"],"seq_region_name":"7","id":"rs538207664","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444835,"source":"dbSNP","strand":1,"feature_type":"variation","end":140444835,"alleles":["G","A","T"],"seq_region_name":"7","id":"rs1585450762","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1268870337","alleles":["G","A"],"end":140444836,"feature_type":"variation","strand":1,"source":"dbSNP","start":140444836,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs890275737","clinical_significance":[],"start":140444839,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","G"],"end":140444839,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1799872035","clinical_significance":[],"alleles":["T","C"],"end":140444841,"strand":1,"feature_type":"variation","start":140444841,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"id":"rs934669171","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140444842,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444842,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799872088","clinical_significance":[],"alleles":["C","A","T"],"end":140444843,"strand":1,"feature_type":"variation","start":140444843,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444846,"source":"dbSNP","strand":1,"feature_type":"variation","end":140444846,"alleles":["G","C"],"seq_region_name":"7","id":"rs1799872123","clinical_significance":[]},{"seq_region_name":"7","id":"rs891986476","clinical_significance":[],"end":140444851,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140444851,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"id":"rs1799872172","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140444854,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444854,"source":"dbSNP"},{"seq_region_name":"7","id":"rs200231320","clinical_significance":[],"start":140444855,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140444855,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1014372195","source":"dbSNP","start":140444857,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140444857,"alleles":["A","G"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140444858,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444858,"source":"dbSNP","id":"rs1403412791","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1352533282","source":"dbSNP","start":140444859,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140444859,"alleles":["T","C"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140444869,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444869,"clinical_significance":[],"seq_region_name":"7","id":"rs1799872298"},{"seq_region_name":"7","id":"rs1799872324","clinical_significance":[],"end":140444873,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140444873,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799872343","end":140444875,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140444875,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"id":"rs1045995078","seq_region_name":"7","clinical_significance":[],"start":140444878,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","A","T"],"end":140444878,"strand":1,"feature_type":"variation"},{"alleles":["G","A","T"],"end":140444879,"feature_type":"variation","strand":1,"source":"dbSNP","start":140444879,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1246184380"},{"id":"rs1799872444","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140444880,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444880,"source":"dbSNP"},{"id":"rs906089113","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140444885,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444885,"source":"dbSNP"},{"alleles":["C","G"],"end":140444886,"strand":1,"feature_type":"variation","start":140444886,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1038950064","clinical_significance":[]},{"start":140444889,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140444889,"alleles":["A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1001825782","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799872554","source":"dbSNP","start":140444890,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140444890,"alleles":["G","GTTCGATCATCATCGG"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1293473970","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444891,"source":"dbSNP","strand":1,"feature_type":"variation","end":140444890,"alleles":["-","TTC"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799872590","source":"dbSNP","start":140444891,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140444891,"feature_type":"variation","strand":1},{"alleles":["-","ATCATCATCGGA"],"end":140444891,"feature_type":"variation","strand":1,"source":"dbSNP","start":140444892,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1356732492","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs568712328","alleles":["C","T"],"end":140444893,"feature_type":"variation","strand":1,"source":"dbSNP","start":140444893,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1000839678","feature_type":"variation","strand":1,"end":140444894,"alleles":["G","A","C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444894},{"end":140444895,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140444895,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799872698","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585450820","feature_type":"variation","strand":1,"end":140444897,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444897},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140444898,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444898,"source":"dbSNP","id":"rs1032431263","seq_region_name":"7","clinical_significance":[]},{"start":140444899,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","A","G"],"end":140444899,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585450827","clinical_significance":[]},{"seq_region_name":"7","id":"rs892517469","clinical_significance":[],"end":140444901,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140444901,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1309575097","clinical_significance":[],"start":140444902,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140444902,"strand":1,"feature_type":"variation"},{"end":140444921,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140444921,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799872834","clinical_significance":[]},{"seq_region_name":"7","id":"rs1481548373","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444923,"source":"dbSNP","strand":1,"feature_type":"variation","end":140444923,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799872878","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444931,"feature_type":"variation","strand":1,"end":140444931,"alleles":["C","A","T"]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140444932,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444932,"source":"dbSNP","seq_region_name":"7","id":"rs1271353969","clinical_significance":[]},{"source":"dbSNP","start":140444933,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140444933,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1010059557","seq_region_name":"7"},{"alleles":["C","T"],"end":140444937,"feature_type":"variation","strand":1,"source":"dbSNP","start":140444937,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs144708357"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1025182104","source":"dbSNP","start":140444940,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140444940,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1799872973","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444941,"source":"dbSNP","strand":1,"feature_type":"variation","end":140444941,"alleles":["T","C"]},{"clinical_significance":[],"id":"rs971287861","seq_region_name":"7","source":"dbSNP","start":140444946,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140444946,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444947,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140444947,"seq_region_name":"7","id":"rs1317839177","clinical_significance":[]},{"alleles":["C","A"],"end":140444949,"strand":1,"feature_type":"variation","start":140444949,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799873033","clinical_significance":[]},{"alleles":["T","G"],"end":140444955,"strand":1,"feature_type":"variation","start":140444955,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs976548588","clinical_significance":[]},{"clinical_significance":[],"id":"rs181303311","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444957,"feature_type":"variation","strand":1,"end":140444957,"alleles":["G","T"]},{"id":"rs1002489773","seq_region_name":"7","clinical_significance":[],"end":140444958,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140444958,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1033866294","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140444959,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444959},{"id":"rs1799873169","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140444962,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444962,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1164517676","source":"dbSNP","start":140444965,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140444965,"alleles":["T","A"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140444966,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444966,"clinical_significance":[],"id":"rs1335588235","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1799874295","seq_region_name":"7","source":"dbSNP","start":140444969,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140444969,"alleles":["G","A"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444971,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140444971,"seq_region_name":"7","id":"rs963035458","clinical_significance":[]},{"seq_region_name":"7","id":"rs973002085","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140444972,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444972,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799874380","clinical_significance":[],"start":140444974,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140444974,"strand":1,"feature_type":"variation"},{"start":140444975,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140444975,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","id":"rs919013102","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444980,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140444980,"clinical_significance":[],"seq_region_name":"7","id":"rs1326637618"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799874514","feature_type":"variation","strand":1,"end":140444981,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140444981},{"seq_region_name":"7","id":"rs10262595","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444988,"source":"dbSNP","strand":1,"feature_type":"variation","end":140444988,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1409193645","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444989,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140444989},{"seq_region_name":"7","id":"rs1164110488","clinical_significance":[],"start":140444992,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140444992,"strand":1,"feature_type":"variation"},{"end":140444993,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140444993,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1385757494","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs950529102","end":140444995,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140444995,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140444996,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140444996,"source":"dbSNP","id":"rs1799874663","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs953920778","clinical_significance":[],"end":140445002,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140445002,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"end":140445003,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140445003,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799874718"},{"start":140445004,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140445004,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs985471939","clinical_significance":[]},{"clinical_significance":[],"id":"rs1296823330","seq_region_name":"7","end":140445007,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140445007,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"alleles":["G","A","T"],"end":140445010,"strand":1,"feature_type":"variation","start":140445010,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs777197050","clinical_significance":[]},{"seq_region_name":"7","id":"rs987622862","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140445016,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445016,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799874863","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445018,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140445018},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445019,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140445019,"seq_region_name":"7","id":"rs1483893241","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585450891","source":"dbSNP","start":140445024,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140445024,"alleles":["A","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs148194693","source":"dbSNP","start":140445026,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140445026,"alleles":["C","T"],"feature_type":"variation","strand":1},{"alleles":["G","A"],"end":140445027,"feature_type":"variation","strand":1,"source":"dbSNP","start":140445027,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs943183413"},{"alleles":["G","A","T"],"end":140445028,"feature_type":"variation","strand":1,"source":"dbSNP","start":140445028,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs935980368"},{"end":140445029,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140445029,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1038982670"},{"seq_region_name":"7","id":"rs925836214","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140445033,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445033,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445034,"source":"dbSNP","strand":1,"feature_type":"variation","end":140445034,"alleles":["A","G"],"seq_region_name":"7","id":"rs10280145","clinical_significance":[]},{"end":140445037,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140445037,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799875225","clinical_significance":[]},{"seq_region_name":"7","id":"rs1311413565","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140445038,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445038,"source":"dbSNP"},{"alleles":["T","G"],"end":140445039,"strand":1,"feature_type":"variation","start":140445039,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1585450918","clinical_significance":[]},{"start":140445041,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140445041,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585450920","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1227267881","source":"dbSNP","start":140445042,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140445042,"feature_type":"variation","strand":1},{"id":"rs368552233","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445043,"source":"dbSNP","strand":1,"feature_type":"variation","end":140445043,"alleles":["G","A","C"]},{"source":"dbSNP","start":140445044,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140445044,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1408989424","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445050,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140445050,"id":"rs1202419395","seq_region_name":"7","clinical_significance":[]},{"end":140445051,"alleles":["G","A","C","T"],"strand":1,"feature_type":"variation","start":140445051,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs892460539","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140445055,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140445055,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1304821396","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs566166370","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445058,"feature_type":"variation","strand":1,"end":140445058,"alleles":["C","T"]},{"alleles":["G","A"],"end":140445059,"feature_type":"variation","strand":1,"source":"dbSNP","start":140445059,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1046906932"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799877032","feature_type":"variation","strand":1,"end":140445061,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445061},{"source":"dbSNP","start":140445063,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140445063,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1185175037","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799877081","clinical_significance":[],"alleles":["C","T"],"end":140445066,"strand":1,"feature_type":"variation","start":140445066,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445068,"source":"dbSNP","strand":1,"feature_type":"variation","end":140445068,"alleles":["C","T"],"seq_region_name":"7","id":"rs1364995424","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585450964","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445069,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140445069},{"clinical_significance":[],"id":"rs1045835092","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445070,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140445070},{"clinical_significance":[],"seq_region_name":"7","id":"rs1421009325","source":"dbSNP","start":140445072,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140445072,"alleles":["A","G"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140445080,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140445080,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1245221440","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140445082,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445082,"clinical_significance":[],"seq_region_name":"7","id":"rs1406045737"},{"seq_region_name":"7","id":"rs1585450977","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445083,"source":"dbSNP","strand":1,"feature_type":"variation","end":140445083,"alleles":["C","A"]},{"seq_region_name":"7","id":"rs1442962866","clinical_significance":[],"end":140445085,"alleles":["AA","A"],"strand":1,"feature_type":"variation","start":140445084,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs146967618","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140445085,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445085,"source":"dbSNP"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445086,"feature_type":"variation","strand":1,"end":140445086,"alleles":["G","A","T"],"clinical_significance":[],"id":"rs1799877283","seq_region_name":"7"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445087,"feature_type":"variation","strand":1,"end":140445087,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1420243786"},{"clinical_significance":[],"id":"rs558205405","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","A","G","T"],"end":140445089,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445089},{"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140445090,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445090,"source":"dbSNP","seq_region_name":"7","id":"rs1169042231","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799877390","clinical_significance":[],"strand":1,"feature_type":"variation","end":140445091,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445091,"source":"dbSNP"},{"start":140445092,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140445092,"alleles":["A","G"],"strand":1,"feature_type":"variation","id":"rs1400173317","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445094,"feature_type":"variation","strand":1,"end":140445094,"alleles":["C","A","G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585451000"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445094,"feature_type":"variation","strand":1,"end":140445097,"alleles":["CTCT","CT"],"clinical_significance":[],"seq_region_name":"7","id":"rs1261864563"},{"alleles":["T","C"],"end":140445095,"strand":1,"feature_type":"variation","start":140445095,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1585451005","clinical_significance":[]},{"seq_region_name":"7","id":"rs1470536534","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140445097,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445097,"source":"dbSNP"},{"end":140445098,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140445098,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1339053733","clinical_significance":[]},{"seq_region_name":"7","id":"rs1215849863","clinical_significance":[],"start":140445099,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140445099,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"start":140445099,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["TCTC","TC"],"end":140445102,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130211433","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs140095064","feature_type":"variation","strand":1,"end":140445100,"alleles":["C","A","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445100},{"feature_type":"variation","strand":1,"end":140445101,"alleles":["T","A","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445101,"clinical_significance":[],"seq_region_name":"7","id":"rs1403485465"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799877623","end":140445101,"alleles":["T","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140445101,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1799877651","clinical_significance":[],"start":140445101,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["TCAA","-"],"end":140445104,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1799877672","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445101,"source":"dbSNP","strand":1,"feature_type":"variation","end":140445105,"alleles":["TCAAA","-"]},{"start":140445102,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["-","A"],"end":140445101,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799877689","clinical_significance":[]},{"source":"dbSNP","start":140445102,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140445102,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1257010244","seq_region_name":"7"},{"alleles":["C","-"],"end":140445102,"strand":1,"feature_type":"variation","start":140445102,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1318256702","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140445103,"alleles":["CA","-"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445102,"source":"dbSNP","seq_region_name":"7","id":"rs1799877753","clinical_significance":[]},{"seq_region_name":"7","id":"rs1304336054","clinical_significance":[],"start":140445102,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["CAAA","-"],"end":140445105,"strand":1,"feature_type":"variation"},{"start":140445102,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140445106,"alleles":["CAAAA","-"],"strand":1,"feature_type":"variation","id":"rs1227419292","seq_region_name":"7","clinical_significance":[]},{"alleles":["CAAAAA","-"],"end":140445107,"feature_type":"variation","strand":1,"source":"dbSNP","start":140445102,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1345859728"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1446753807","source":"dbSNP","start":140445103,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140445103,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140445103,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140445103,"alleles":["A","ACAAA"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799877848"},{"start":140445103,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140445129,"alleles":["AAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAA","AAAAAAAAAAAAAA","AAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA"],"strand":1,"feature_type":"variation","id":"rs35208054","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1270288629","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140445105,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445105,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1363536280","seq_region_name":"7","alleles":["A","C","T"],"end":140445106,"feature_type":"variation","strand":1,"source":"dbSNP","start":140445106,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"alleles":["A","C"],"end":140445107,"feature_type":"variation","strand":1,"source":"dbSNP","start":140445107,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1212260921"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799878169","feature_type":"variation","strand":1,"end":140445109,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445109},{"start":140445116,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140445116,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1563081678","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140445116,"alleles":["-","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445117,"source":"dbSNP","seq_region_name":"7","id":"rs1390935687","clinical_significance":[]},{"seq_region_name":"7","id":"rs1324120696","clinical_significance":[],"start":140445117,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140445117,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140445118,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445118,"source":"dbSNP","seq_region_name":"7","id":"rs1563081683","clinical_significance":[]},{"source":"dbSNP","start":140445121,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140445121,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799878255"},{"end":140445121,"alleles":["-","G"],"strand":1,"feature_type":"variation","start":140445122,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799878275","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445125,"feature_type":"variation","strand":1,"end":140445125,"alleles":["A","G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799878297"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799878319","alleles":["AA","AATAA"],"end":140445127,"feature_type":"variation","strand":1,"source":"dbSNP","start":140445126,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"alleles":["AAAAT","-"],"end":140445130,"feature_type":"variation","strand":1,"source":"dbSNP","start":140445126,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130211550"},{"end":140445127,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140445127,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1264673396","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140445128,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140445128,"alleles":["A","C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs78596077"},{"seq_region_name":"7","id":"rs2130211563","clinical_significance":[],"start":140445128,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","AGA"],"end":140445128,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140445129,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445129,"source":"dbSNP","seq_region_name":"7","id":"rs60198071","clinical_significance":[]},{"start":140445130,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["-","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAG","AAAAAAAAAAAAG","AAAAAAAAAAAG","AAAAAAAAAAG","AAAAAAG","AAAAG","AAG","AG","G"],"end":140445129,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs765108307","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1205363327","source":"dbSNP","start":140445130,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140445130,"alleles":["T","A"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140445130,"alleles":["T","-"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445130,"clinical_significance":[],"seq_region_name":"7","id":"rs1799878548"},{"alleles":["TC","-"],"end":140445131,"strand":1,"feature_type":"variation","start":140445130,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs375093045","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1260949598","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445131,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140445131},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445133,"source":"dbSNP","strand":1,"feature_type":"variation","end":140445133,"alleles":["A","G"],"seq_region_name":"7","id":"rs1359894225","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1440921755","feature_type":"variation","strand":1,"end":140445134,"alleles":["T","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445134},{"seq_region_name":"7","id":"rs1799878656","clinical_significance":[],"end":140445135,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140445135,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1209752514","clinical_significance":[],"strand":1,"feature_type":"variation","end":140445136,"alleles":["T","A","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445136,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140445137,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445137,"source":"dbSNP","seq_region_name":"7","id":"rs1002306818","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799878717","clinical_significance":[],"start":140445138,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","A","T"],"end":140445138,"strand":1,"feature_type":"variation"},{"id":"rs1799878735","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445141,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C","T"],"end":140445141},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445142,"feature_type":"variation","strand":1,"end":140445142,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799878757"},{"seq_region_name":"7","id":"rs1799878781","clinical_significance":[],"start":140445143,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140445143,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1033893870","seq_region_name":"7","alleles":["A","C","G","T"],"end":140445144,"feature_type":"variation","strand":1,"source":"dbSNP","start":140445144,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445145,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140445145,"clinical_significance":[],"id":"rs2130211628","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140445146,"alleles":["T","C","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445146,"clinical_significance":[],"seq_region_name":"7","id":"rs1585451109"},{"clinical_significance":[],"seq_region_name":"7","id":"rs963561374","end":140445148,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140445148,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140445153,"alleles":["GTTCGT","GTTCGTTCGT"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445148,"clinical_significance":[],"seq_region_name":"7","id":"rs1799878861"},{"start":140445150,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140445150,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130211642","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445151,"feature_type":"variation","strand":1,"end":140445151,"alleles":["C","T"],"clinical_significance":[],"id":"rs995041019","seq_region_name":"7"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445152,"feature_type":"variation","strand":1,"end":140445152,"alleles":["G","A","T"],"clinical_significance":[],"id":"rs117400339","seq_region_name":"7"},{"end":140445154,"alleles":["A","C","G","T"],"strand":1,"feature_type":"variation","start":140445154,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799878942","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130211669","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445157,"source":"dbSNP","strand":1,"feature_type":"variation","end":140445157,"alleles":["T","A"]},{"clinical_significance":[],"id":"rs1453519756","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140445158,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445158},{"seq_region_name":"7","id":"rs1799878990","clinical_significance":[],"strand":1,"feature_type":"variation","end":140445162,"alleles":["T","TT"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445162,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140445164,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445164,"source":"dbSNP","id":"rs1799879006","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445165,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140445165,"clinical_significance":[],"id":"rs1799879021","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585451126","source":"dbSNP","start":140445166,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140445166,"feature_type":"variation","strand":1},{"end":140445168,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140445168,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs2130211689","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799879064","end":140445170,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140445170,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs2130211695","seq_region_name":"7","source":"dbSNP","start":140445172,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140445172,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140445180,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445180,"source":"dbSNP","id":"rs1799879089","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445185,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140445185,"seq_region_name":"7","id":"rs1799879107","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585451128","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445186,"source":"dbSNP","strand":1,"feature_type":"variation","end":140445186,"alleles":["T","G"]},{"source":"dbSNP","start":140445189,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140445189,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs950415814","seq_region_name":"7"},{"alleles":["A","G"],"end":140445192,"feature_type":"variation","strand":1,"source":"dbSNP","start":140445192,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799879164"},{"alleles":["C","T"],"end":140445205,"strand":1,"feature_type":"variation","start":140445205,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799879184","clinical_significance":[]},{"seq_region_name":"7","id":"rs1563081714","clinical_significance":[],"strand":1,"feature_type":"variation","end":140445210,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445210,"source":"dbSNP"},{"alleles":["A","C"],"end":140445217,"feature_type":"variation","strand":1,"source":"dbSNP","start":140445217,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1408541478"},{"seq_region_name":"7","id":"rs1799879259","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445218,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140445218},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140445219,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445219,"source":"dbSNP","seq_region_name":"7","id":"rs1585451137","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445223,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140445223,"seq_region_name":"7","id":"rs1799879298","clinical_significance":[]},{"alleles":["G","A"],"end":140445225,"strand":1,"feature_type":"variation","start":140445225,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1174619061","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","C"],"end":140445226,"strand":1,"feature_type":"variation","start":140445226,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1191571022","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799879361","seq_region_name":"7","feature_type":"variation","strand":1,"end":140445231,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445231},{"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140445243,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445243,"clinical_significance":[],"seq_region_name":"7","id":"rs987266536"},{"clinical_significance":[],"id":"rs1799879402","seq_region_name":"7","end":140445244,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140445244,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs888160577","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445245,"source":"dbSNP","strand":1,"feature_type":"variation","end":140445245,"alleles":["A","C"]},{"source":"dbSNP","start":140445257,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140445257,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130211750"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445258,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140445258,"clinical_significance":[],"seq_region_name":"7","id":"rs1423573935"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445258,"feature_type":"variation","strand":1,"alleles":["AAAAA","AAAAAA"],"end":140445262,"clinical_significance":[],"seq_region_name":"7","id":"rs1799879467"},{"id":"rs911602149","seq_region_name":"7","clinical_significance":[],"start":140445259,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140445259,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585451153","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140445263,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445263},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140445264,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445264,"source":"dbSNP","seq_region_name":"7","id":"rs1173109937","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799879540","seq_region_name":"7","feature_type":"variation","strand":1,"end":140445267,"alleles":["C","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445267},{"clinical_significance":[],"seq_region_name":"7","id":"rs1427294696","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445268,"feature_type":"variation","strand":1,"end":140445268,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1718422697","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445273,"source":"dbSNP","strand":1,"feature_type":"variation","end":140445273,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs964593680","clinical_significance":[],"alleles":["G","A","C"],"end":140445275,"strand":1,"feature_type":"variation","start":140445275,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140445277,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445277,"source":"dbSNP","seq_region_name":"7","id":"rs1799879603","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445278,"feature_type":"variation","strand":1,"end":140445278,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799879625"},{"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140445289,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445289,"source":"dbSNP","id":"rs974540647","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140445291,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445291,"source":"dbSNP","seq_region_name":"7","id":"rs191712263","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1427571151","end":140445295,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140445295,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799879725","source":"dbSNP","start":140445299,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140445299,"alleles":["C","T"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140445304,"alleles":["T","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445304,"clinical_significance":[],"seq_region_name":"7","id":"rs1461425532"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445310,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140445310,"seq_region_name":"7","id":"rs1244592422","clinical_significance":[]},{"seq_region_name":"7","id":"rs1015351639","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445314,"source":"dbSNP","strand":1,"feature_type":"variation","end":140445314,"alleles":["G","A"]},{"id":"rs1414253438","seq_region_name":"7","clinical_significance":[],"start":140445316,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140445316,"strand":1,"feature_type":"variation"},{"start":140445320,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140445320,"strand":1,"feature_type":"variation","id":"rs925768986","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445324,"feature_type":"variation","strand":1,"end":140445324,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs896869584"},{"clinical_significance":[],"id":"rs1799879844","seq_region_name":"7","alleles":["T","C"],"end":140445325,"feature_type":"variation","strand":1,"source":"dbSNP","start":140445325,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1585451185","seq_region_name":"7","alleles":["T","C"],"end":140445329,"feature_type":"variation","strand":1,"source":"dbSNP","start":140445329,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445329,"feature_type":"variation","strand":1,"alleles":["TT","TTT"],"end":140445330,"clinical_significance":[],"seq_region_name":"7","id":"rs761838212"},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140445332,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445332,"clinical_significance":[],"seq_region_name":"7","id":"rs1799879905"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445342,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140445342,"seq_region_name":"7","id":"rs10225361","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799879960","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140445345,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445345,"source":"dbSNP"},{"source":"dbSNP","start":140445351,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140445351,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1305659483","seq_region_name":"7"},{"id":"rs1799879989","seq_region_name":"7","clinical_significance":[],"start":140445357,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140445357,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799880014","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445360,"feature_type":"variation","strand":1,"alleles":["T","TT"],"end":140445360},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445362,"feature_type":"variation","strand":1,"end":140445362,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs541799709"},{"alleles":["T","C"],"end":140445366,"feature_type":"variation","strand":1,"source":"dbSNP","start":140445366,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799880081"},{"alleles":["A","C"],"end":140445377,"strand":1,"feature_type":"variation","start":140445377,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1585451200","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140445380,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445380,"source":"dbSNP","seq_region_name":"7","id":"rs953845330","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799880158","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140445385,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445385,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1334902654","source":"dbSNP","start":140445388,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140445388,"alleles":["G","A"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140445389,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445389,"source":"dbSNP","seq_region_name":"7","id":"rs1799880206","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs560466034","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140445390,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445390},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799880243","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445394,"feature_type":"variation","strand":1,"end":140445394,"alleles":["A","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130211900","end":140445394,"alleles":["A","AA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140445394,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1395698021","seq_region_name":"7","alleles":["G","-"],"end":140445395,"feature_type":"variation","strand":1,"source":"dbSNP","start":140445395,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130211908","source":"dbSNP","start":140445399,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140445399,"feature_type":"variation","strand":1},{"alleles":["G","A"],"end":140445401,"strand":1,"feature_type":"variation","start":140445401,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs2130211914","clinical_significance":[]},{"end":140445403,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140445403,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130211921"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445405,"source":"dbSNP","strand":1,"feature_type":"variation","end":140445405,"alleles":["C","A"],"id":"rs1397613277","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1745481212","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445409,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140445409},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445410,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140445410,"seq_region_name":"7","id":"rs1346072973","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140445411,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445411,"source":"dbSNP","seq_region_name":"7","id":"rs1390090954","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445412,"feature_type":"variation","strand":1,"alleles":["AAAAAAAAAA","AAAAAAAAA","AAAAAAAAAAA","AAAAAAAAAAAA"],"end":140445421,"clinical_significance":[],"seq_region_name":"7","id":"rs371243530"},{"source":"dbSNP","start":140445422,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140445422,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585451222"},{"start":140445424,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","G","T"],"end":140445424,"strand":1,"feature_type":"variation","id":"rs548265837","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1386571500","clinical_significance":[],"start":140445428,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","A","G"],"end":140445428,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1281284764","alleles":["G","T"],"end":140445430,"feature_type":"variation","strand":1,"source":"dbSNP","start":140445430,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445438,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140445438,"clinical_significance":[],"seq_region_name":"7","id":"rs1799880486"},{"seq_region_name":"7","id":"rs1250845818","clinical_significance":[],"start":140445438,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140445441,"alleles":["CAGC","CAGCCAGC"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140445439,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140445439,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1033338959"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445440,"source":"dbSNP","strand":1,"feature_type":"variation","end":140445440,"alleles":["G","A"],"seq_region_name":"7","id":"rs1479566985","clinical_significance":[]},{"seq_region_name":"7","id":"rs772473836","clinical_significance":[],"start":140445441,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140445441,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"start":140445441,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","CC"],"end":140445441,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1344123910","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140445442,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445442,"source":"dbSNP","seq_region_name":"7","id":"rs2130212006","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs183494761","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140445443,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445443},{"id":"rs1563081748","seq_region_name":"7","clinical_significance":[],"start":140445444,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140445444,"alleles":["C","CAAC"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1246624911","source":"dbSNP","start":140445444,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140445449,"alleles":["CCCCCC","CCCCC","CCCCCCC","CCCCCCCCCCCCC"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140445449,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445449,"clinical_significance":[],"seq_region_name":"7","id":"rs1799880724"},{"feature_type":"variation","strand":1,"end":140445450,"alleles":["A","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445450,"clinical_significance":[],"seq_region_name":"7","id":"rs1799880744"},{"strand":1,"feature_type":"variation","end":140445452,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445452,"source":"dbSNP","seq_region_name":"7","id":"rs1046496801","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130212033","alleles":["A","C"],"end":140445453,"feature_type":"variation","strand":1,"source":"dbSNP","start":140445453,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445455,"source":"dbSNP","strand":1,"feature_type":"variation","end":140445455,"alleles":["C","T"],"seq_region_name":"7","id":"rs906573500","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445456,"source":"dbSNP","strand":1,"feature_type":"variation","end":140445456,"alleles":["G","A","C"],"id":"rs544086165","seq_region_name":"7","clinical_significance":[]},{"id":"rs1799880904","seq_region_name":"7","clinical_significance":[],"start":140445457,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140445457,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"end":140445459,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140445459,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs373768093"},{"strand":1,"feature_type":"variation","end":140445462,"alleles":["A","C","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445462,"source":"dbSNP","id":"rs1799880950","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs564555942","alleles":["G","A","C"],"end":140445463,"feature_type":"variation","strand":1,"source":"dbSNP","start":140445463,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs57938495","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140445464,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445464},{"seq_region_name":"7","id":"rs77193809","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445466,"source":"dbSNP","strand":1,"feature_type":"variation","end":140445466,"alleles":["T","A","G"]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445466,"source":"dbSNP","strand":1,"feature_type":"variation","end":140445470,"alleles":["TTTTT","TTT"],"seq_region_name":"7","id":"rs1309497659","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140445470,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445470,"clinical_significance":[],"seq_region_name":"7","id":"rs1490661476"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445471,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140445471,"seq_region_name":"7","id":"rs1304223294","clinical_significance":[]},{"source":"dbSNP","start":140445475,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140445475,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1427133779"},{"seq_region_name":"7","id":"rs1366851093","clinical_significance":[],"start":140445477,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140445477,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"start":140445480,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140445480,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130212106","clinical_significance":[]},{"end":140445482,"alleles":["GGG","GGGG"],"strand":1,"feature_type":"variation","start":140445480,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799881218","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1026968028","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445481,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140445481},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799881250","source":"dbSNP","start":140445482,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140445482,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs886118536","feature_type":"variation","strand":1,"end":140445484,"alleles":["C","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445484},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445486,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140445486,"seq_region_name":"7","id":"rs1799881291","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445491,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140445491,"clinical_significance":[],"seq_region_name":"7","id":"rs1799881307"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1008955928","feature_type":"variation","strand":1,"end":140445492,"alleles":["G","A","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445492},{"id":"rs937510221","seq_region_name":"7","clinical_significance":[],"start":140445500,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140445500,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1183618310","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445503,"feature_type":"variation","strand":1,"end":140445503,"alleles":["T","C"]},{"end":140445507,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140445507,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1049355444","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1250834682","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140445508,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445508},{"seq_region_name":"7","id":"rs1585451311","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445516,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140445516},{"clinical_significance":[],"seq_region_name":"7","id":"rs1223088093","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140445518,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445518},{"end":140445519,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140445519,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799881446","clinical_significance":[]},{"end":140445521,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140445521,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1490812611","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585451315","clinical_significance":[],"start":140445523,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","A"],"end":140445523,"strand":1,"feature_type":"variation"},{"end":140445525,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140445525,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1289572621"},{"clinical_significance":[],"id":"rs1477931740","seq_region_name":"7","source":"dbSNP","start":140445527,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140445527,"alleles":["C","T"],"feature_type":"variation","strand":1},{"id":"rs1018699125","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445528,"source":"dbSNP","strand":1,"feature_type":"variation","end":140445528,"alleles":["G","A"]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445534,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140445534,"seq_region_name":"7","id":"rs887993879","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445535,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140445535,"id":"rs964490772","seq_region_name":"7","clinical_significance":[]},{"start":140445538,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140445538,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs1237174644","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs974488237","clinical_significance":[],"alleles":["C","T"],"end":140445540,"strand":1,"feature_type":"variation","start":140445540,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1407188080","source":"dbSNP","start":140445542,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140445542,"feature_type":"variation","strand":1},{"end":140445556,"alleles":["CTGTGGGCCTCAAAC","-"],"strand":1,"feature_type":"variation","start":140445542,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1284360714","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130212205","clinical_significance":[],"start":140445543,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","A"],"end":140445543,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563081783","source":"dbSNP","start":140445544,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140445544,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799881676","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140445546,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445546},{"clinical_significance":[],"seq_region_name":"7","id":"rs1344147567","source":"dbSNP","start":140445547,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140445547,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130212224","end":140445549,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140445549,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"start":140445553,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","C","G"],"end":140445553,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1032869873","clinical_significance":[]},{"id":"rs1404232792","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445556,"source":"dbSNP","strand":1,"feature_type":"variation","end":140445556,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799881761","source":"dbSNP","start":140445559,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140445559,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140445563,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445563,"source":"dbSNP","seq_region_name":"7","id":"rs1799881784","clinical_significance":[]},{"end":140445571,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140445571,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1037082756","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799881836","clinical_significance":[],"start":140445573,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","A"],"end":140445573,"strand":1,"feature_type":"variation"},{"start":140445582,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140445582,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs10275127","clinical_significance":[]},{"id":"rs2130212270","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140445588,"strand":1,"feature_type":"variation","start":140445588,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445590,"source":"dbSNP","strand":1,"feature_type":"variation","end":140445592,"alleles":["CCC","CCCC"],"id":"rs1799881911","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140445591,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445591,"source":"dbSNP","seq_region_name":"7","id":"rs1455347531","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799881957","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445592,"feature_type":"variation","strand":1,"end":140445592,"alleles":["C","T"]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140445593,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445593,"clinical_significance":[],"seq_region_name":"7","id":"rs535849833"},{"seq_region_name":"7","id":"rs913119840","clinical_significance":[],"start":140445594,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","A","C"],"end":140445594,"strand":1,"feature_type":"variation"},{"end":140445595,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140445595,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1199858261"},{"end":140445604,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140445604,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1029399550","clinical_significance":[]},{"clinical_significance":[],"id":"rs1244907152","seq_region_name":"7","source":"dbSNP","start":140445605,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140445605,"feature_type":"variation","strand":1},{"end":140445606,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140445606,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs945402660","clinical_significance":[]},{"source":"dbSNP","start":140445613,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["CACC","CACCACC"],"end":140445616,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1365719707"},{"clinical_significance":[],"id":"rs1799882099","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445615,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140445615},{"clinical_significance":[],"seq_region_name":"7","id":"rs1198084102","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445616,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140445616},{"alleles":["G","A"],"end":140445617,"strand":1,"feature_type":"variation","start":140445617,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1406241771","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140445620,"alleles":["C","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445620,"clinical_significance":[],"seq_region_name":"7","id":"rs545996588"},{"start":140445624,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140445626,"alleles":["CCC","CCCCCC"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs747824030","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs547729102","feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140445628,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445628},{"seq_region_name":"7","id":"rs1799882252","clinical_significance":[],"start":140445630,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140445630,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1264041347","feature_type":"variation","strand":1,"end":140445631,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445631},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799882283","end":140445633,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140445633,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445634,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140445634,"clinical_significance":[],"seq_region_name":"7","id":"rs1225716806"},{"seq_region_name":"7","id":"rs957474451","clinical_significance":[],"start":140445636,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","C"],"end":140445636,"strand":1,"feature_type":"variation"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445637,"feature_type":"variation","strand":1,"end":140445637,"alleles":["A","G"],"clinical_significance":[],"id":"rs539613234","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445652,"source":"dbSNP","strand":1,"feature_type":"variation","end":140445652,"alleles":["A","C"],"seq_region_name":"7","id":"rs558856267","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799882404","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140445660,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445660},{"feature_type":"variation","strand":1,"alleles":["GGG","GG"],"end":140445662,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445660,"clinical_significance":[],"seq_region_name":"7","id":"rs1799882430"},{"source":"dbSNP","start":140445661,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140445661,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs116792060","seq_region_name":"7"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445665,"feature_type":"variation","strand":1,"alleles":["AAAAGAAAA","AAAA"],"end":140445673,"clinical_significance":[],"seq_region_name":"7","id":"rs1799882476"},{"source":"dbSNP","start":140445668,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140445668,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs2130212381","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445670,"source":"dbSNP","strand":1,"feature_type":"variation","end":140445670,"alleles":["A","G"],"seq_region_name":"7","id":"rs899368421","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140445673,"alleles":["AAAA","AAA"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445670,"clinical_significance":[],"id":"rs1319685640","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140445677,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445677,"source":"dbSNP","id":"rs930783715","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1387442036","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445682,"feature_type":"variation","strand":1,"end":140445683,"alleles":["CC","C"]},{"end":140445685,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140445685,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1281034625","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs971355622","source":"dbSNP","start":140445687,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140445687,"alleles":["G","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs981532587","clinical_significance":[],"alleles":["T","C"],"end":140445692,"strand":1,"feature_type":"variation","start":140445692,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs528479965","source":"dbSNP","start":140445693,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140445693,"feature_type":"variation","strand":1},{"start":140445694,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A","T"],"end":140445694,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1238176104","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140445695,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445695,"source":"dbSNP","seq_region_name":"7","id":"rs1047994452","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799882781","clinical_significance":[],"strand":1,"feature_type":"variation","end":140445699,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445699,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1243813148","alleles":["G","A"],"end":140445701,"feature_type":"variation","strand":1,"source":"dbSNP","start":140445701,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"alleles":["G","A"],"end":140445702,"strand":1,"feature_type":"variation","start":140445702,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs188893681","seq_region_name":"7","clinical_significance":[]},{"id":"rs1009143914","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445703,"source":"dbSNP","strand":1,"feature_type":"variation","end":140445703,"alleles":["C","T"]},{"id":"rs1464546833","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140445704,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445704,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1243967776","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140445705,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445705},{"start":140445713,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140445713,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1205808326","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445714,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140445714,"clinical_significance":[],"seq_region_name":"7","id":"rs537593337"},{"clinical_significance":[],"seq_region_name":"7","id":"rs772668400","feature_type":"variation","strand":1,"alleles":["A","-"],"end":140445715,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445715},{"id":"rs1799883004","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140445716,"alleles":["G","C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445716,"source":"dbSNP"},{"end":140445717,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140445717,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1215567207","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140445718,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140445718,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1342062859"},{"id":"rs1268996751","seq_region_name":"7","clinical_significance":[],"end":140445721,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140445721,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs577432362","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445723,"source":"dbSNP","strand":1,"feature_type":"variation","end":140445723,"alleles":["T","C"]},{"alleles":["A","G"],"end":140445732,"feature_type":"variation","strand":1,"source":"dbSNP","start":140445732,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799883095","seq_region_name":"7"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445733,"feature_type":"variation","strand":1,"end":140445733,"alleles":["C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1363838548"},{"seq_region_name":"7","id":"rs900151162","clinical_significance":[],"alleles":["C","G"],"end":140445740,"strand":1,"feature_type":"variation","start":140445740,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs985325741","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445750,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140445750},{"clinical_significance":[],"id":"rs1451495890","seq_region_name":"7","end":140445751,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140445751,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1799883199","clinical_significance":[],"strand":1,"feature_type":"variation","end":140445751,"alleles":["G","-"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445751,"source":"dbSNP"},{"seq_region_name":"7","id":"rs909485594","clinical_significance":[],"strand":1,"feature_type":"variation","end":140445753,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445753,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1410370581","alleles":["T","C"],"end":140445757,"feature_type":"variation","strand":1,"source":"dbSNP","start":140445757,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs6464773","clinical_significance":[],"start":140445758,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","C","G","T"],"end":140445758,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1448865893","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140445759,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445759,"source":"dbSNP"},{"source":"dbSNP","start":140445762,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140445762,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1385954131"},{"start":140445763,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140445763,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1234899775","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799883509","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445765,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140445765},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799883543","alleles":["G","A"],"end":140445770,"feature_type":"variation","strand":1,"source":"dbSNP","start":140445770,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"start":140445774,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","G"],"end":140445774,"strand":1,"feature_type":"variation","id":"rs1185597300","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","T"],"end":140445775,"feature_type":"variation","strand":1,"source":"dbSNP","start":140445775,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs754261434"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1237171297","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445777,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140445777},{"seq_region_name":"7","id":"rs562054907","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140445778,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445778,"source":"dbSNP"},{"source":"dbSNP","start":140445779,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["AGTA","AGTAAGTA"],"end":140445782,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs771369133"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799883707","source":"dbSNP","start":140445788,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140445788,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799883731","source":"dbSNP","start":140445789,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140445789,"alleles":["C","T"],"feature_type":"variation","strand":1},{"start":140445792,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140445792,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs73735251","clinical_significance":[]},{"end":140445793,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140445793,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1385437585","clinical_significance":[]},{"source":"dbSNP","start":140445794,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140445793,"alleles":["-","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799883800"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799883817","alleles":["T","A"],"end":140445794,"feature_type":"variation","strand":1,"source":"dbSNP","start":140445794,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1050864151","clinical_significance":[],"start":140445798,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140445798,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs889503798","clinical_significance":[],"end":140445805,"alleles":["ATA","A"],"strand":1,"feature_type":"variation","start":140445803,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1315181798","clinical_significance":[],"start":140445804,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140445804,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1229574678","clinical_significance":[],"start":140445806,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140445806,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs989013971","seq_region_name":"7","source":"dbSNP","start":140445807,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140445807,"alleles":["A","T"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140445816,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140445816,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1020210918"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445820,"feature_type":"variation","strand":1,"end":140445820,"alleles":["A","C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1006726112"},{"seq_region_name":"7","id":"rs1799883988","clinical_significance":[],"end":140445826,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140445826,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1356063873","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140445827,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445827,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140445838,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445838,"source":"dbSNP","seq_region_name":"7","id":"rs182266499","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799884036","end":140445843,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140445843,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140445847,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140445852,"alleles":["AGACAG","AG"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799884050","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799884072","clinical_significance":[],"start":140445854,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140445854,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs893064169","alleles":["T","G"],"end":140445860,"feature_type":"variation","strand":1,"source":"dbSNP","start":140445860,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1389965948","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445875,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140445875},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445878,"source":"dbSNP","strand":1,"feature_type":"variation","end":140445878,"alleles":["T","C"],"seq_region_name":"7","id":"rs1366225938","clinical_significance":[]},{"alleles":["A","G"],"end":140445879,"strand":1,"feature_type":"variation","start":140445879,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1165526592","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799884180","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140445881,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445881,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140445888,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445888,"clinical_significance":[],"seq_region_name":"7","id":"rs981376488"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1422199551","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140445889,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445889},{"seq_region_name":"7","id":"rs927990993","clinical_significance":[],"start":140445890,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140445890,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs560451944","clinical_significance":[],"alleles":["A","G"],"end":140445897,"strand":1,"feature_type":"variation","start":140445897,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1413346823","end":140445901,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140445901,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1178005028","source":"dbSNP","start":140445903,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140445903,"alleles":["C","G","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs762010604","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140445907,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445907,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140445908,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445908,"source":"dbSNP","seq_region_name":"7","id":"rs1250094835","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445909,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140445909,"clinical_significance":[],"id":"rs80034039","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1490647895","feature_type":"variation","strand":1,"alleles":["CTTAACTT","CTT"],"end":140445920,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445913},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445914,"source":"dbSNP","strand":1,"feature_type":"variation","end":140445915,"alleles":["TT","TTT"],"seq_region_name":"7","id":"rs1799884452","clinical_significance":[]},{"seq_region_name":"7","id":"rs545995430","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140445921,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445921,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445924,"source":"dbSNP","strand":1,"feature_type":"variation","end":140445924,"alleles":["T","C"],"seq_region_name":"7","id":"rs1799884494","clinical_significance":[]},{"id":"rs879213093","seq_region_name":"7","clinical_significance":[],"alleles":["A","G"],"end":140445925,"strand":1,"feature_type":"variation","start":140445925,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799884520","end":140445925,"alleles":["A","AA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140445925,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"alleles":["T","C"],"end":140445932,"strand":1,"feature_type":"variation","start":140445932,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1223108250","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs930815025","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445934,"feature_type":"variation","strand":1,"end":140445934,"alleles":["T","C"]},{"start":140445935,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140445935,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1048327552","clinical_significance":[]},{"clinical_significance":[],"id":"rs908033881","seq_region_name":"7","end":140445940,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140445940,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs944977133","feature_type":"variation","strand":1,"end":140445944,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445944},{"clinical_significance":[],"id":"rs1034399632","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445948,"feature_type":"variation","strand":1,"end":140445948,"alleles":["G","A","C"]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445949,"feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140445949,"clinical_significance":[],"seq_region_name":"7","id":"rs1585451616"},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140445950,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445950,"clinical_significance":[],"seq_region_name":"7","id":"rs1799884697"},{"id":"rs12155423","seq_region_name":"7","clinical_significance":[],"end":140445953,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140445953,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140445954,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445954,"source":"dbSNP","seq_region_name":"7","id":"rs1799884853","clinical_significance":[]},{"start":140445956,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140445956,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130212770","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1308861213","end":140445958,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140445958,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1383734379","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140445962,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445962},{"feature_type":"variation","strand":1,"end":140445968,"alleles":["A","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445968,"clinical_significance":[],"seq_region_name":"7","id":"rs1799884917"},{"clinical_significance":[],"id":"rs1799884938","seq_region_name":"7","end":140445973,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140445973,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445976,"feature_type":"variation","strand":1,"end":140445976,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs531822123"},{"seq_region_name":"7","id":"rs984989803","clinical_significance":[],"alleles":["C","T"],"end":140445977,"strand":1,"feature_type":"variation","start":140445977,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1263686440","feature_type":"variation","strand":1,"end":140445983,"alleles":["A","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140445983},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140445985,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445985,"source":"dbSNP","seq_region_name":"7","id":"rs1799885041","clinical_significance":[]},{"id":"rs1356275006","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140445993,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140445993,"source":"dbSNP"},{"id":"rs10278552","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140445999,"strand":1,"feature_type":"variation","start":140445999,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140446000,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446000,"source":"dbSNP","seq_region_name":"7","id":"rs1799885139","clinical_significance":[]},{"start":140446001,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140446001,"alleles":["G","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799885160","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140446002,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446002,"clinical_significance":[],"id":"rs1799885181","seq_region_name":"7"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446004,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140446004,"clinical_significance":[],"id":"rs1799885199","seq_region_name":"7"},{"clinical_significance":[],"id":"rs186930081","seq_region_name":"7","source":"dbSNP","start":140446006,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140446006,"alleles":["A","G","T"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["T","TT"],"end":140446007,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446007,"source":"dbSNP","seq_region_name":"7","id":"rs1799885246","clinical_significance":[]},{"id":"rs1349385338","seq_region_name":"7","clinical_significance":[],"end":140446008,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140446008,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"source":"dbSNP","start":140446011,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140446011,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1160042997","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs529244802","feature_type":"variation","strand":1,"end":140446013,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446013},{"id":"rs191703477","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140446014,"strand":1,"feature_type":"variation","start":140446014,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"source":"dbSNP","start":140446021,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140446021,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799885351","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446028,"source":"dbSNP","strand":1,"feature_type":"variation","end":140446028,"alleles":["A","C"],"seq_region_name":"7","id":"rs1799885375","clinical_significance":[]},{"end":140446029,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140446029,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1198386246","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs566018582","end":140446030,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140446030,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1009978805","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140446031,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446031},{"clinical_significance":[],"seq_region_name":"7","id":"rs184783051","alleles":["G","A"],"end":140446034,"feature_type":"variation","strand":1,"source":"dbSNP","start":140446034,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs2130212890","clinical_significance":[],"alleles":["T","G"],"end":140446038,"strand":1,"feature_type":"variation","start":140446038,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"alleles":["C","A"],"end":140446041,"feature_type":"variation","strand":1,"source":"dbSNP","start":140446041,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799885503"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1189987035","source":"dbSNP","start":140446043,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140446043,"alleles":["G","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs933651500","clinical_significance":[],"strand":1,"feature_type":"variation","end":140446044,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446044,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1184787495","clinical_significance":[],"start":140446046,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140446046,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1216010384","seq_region_name":"7","end":140446057,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140446057,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140446060,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446060,"clinical_significance":[],"id":"rs1563081931","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs971235059","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140446061,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446061},{"end":140446062,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140446062,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs372215163"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1330730022","source":"dbSNP","start":140446063,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","C","G"],"end":140446063,"feature_type":"variation","strand":1},{"start":140446064,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140446064,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1265921058","clinical_significance":[]},{"end":140446067,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140446067,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs2130212924","clinical_significance":[]},{"source":"dbSNP","start":140446072,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140446072,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1003229687","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1227553733","source":"dbSNP","start":140446076,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140446076,"alleles":["G","C"],"feature_type":"variation","strand":1},{"start":140446081,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140446081,"strand":1,"feature_type":"variation","id":"rs1324008976","seq_region_name":"7","clinical_significance":[]},{"end":140446082,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140446082,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1367324136","clinical_significance":[]},{"seq_region_name":"7","id":"rs1303249990","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446085,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140446085},{"seq_region_name":"7","id":"rs201835381","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140446087,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446087,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799885843","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446088,"source":"dbSNP","strand":1,"feature_type":"variation","end":140446088,"alleles":["C","G"]},{"id":"rs1563081940","seq_region_name":"7","clinical_significance":[],"start":140446090,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A","T"],"end":140446090,"strand":1,"feature_type":"variation"},{"alleles":["GG","G"],"end":140446093,"feature_type":"variation","strand":1,"source":"dbSNP","start":140446092,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1366950553"},{"seq_region_name":"7","id":"rs1475450797","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140446093,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446093,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1169652346","clinical_significance":[],"start":140446095,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140446095,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140446099,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140446099,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1386708535","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140446104,"alleles":["C","G","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446104,"clinical_significance":[],"seq_region_name":"7","id":"rs1799885980"},{"source":"dbSNP","start":140446108,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140446108,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585451734"},{"clinical_significance":[],"id":"rs1585451740","seq_region_name":"7","end":140446114,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140446114,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1158790677","clinical_significance":[],"alleles":["C","A","T"],"end":140446121,"strand":1,"feature_type":"variation","start":140446121,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446124,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140446124,"seq_region_name":"7","id":"rs1470468850","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799886099","clinical_significance":[],"end":140446125,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140446125,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1431919541","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446128,"feature_type":"variation","strand":1,"end":140446128,"alleles":["G","T"]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140446129,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446129,"clinical_significance":[],"id":"rs1174511705","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140446131,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446131,"source":"dbSNP","id":"rs1433144128","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs537663283","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446134,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140446134},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130212985","alleles":["C","A"],"end":140446135,"feature_type":"variation","strand":1,"source":"dbSNP","start":140446135,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"start":140446138,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140446138,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs555955800","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140446140,"alleles":["AA","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446139,"clinical_significance":[],"seq_region_name":"7","id":"rs2130212992"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1356636753","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446143,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140446143},{"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140446144,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446144,"clinical_significance":[],"seq_region_name":"7","id":"rs574489458"},{"source":"dbSNP","start":140446145,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140446145,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs990741493"},{"id":"rs2130213010","seq_region_name":"7","clinical_significance":[],"start":140446147,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140446147,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1407116794","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446150,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140446150},{"clinical_significance":[],"id":"rs1245752585","seq_region_name":"7","source":"dbSNP","start":140446151,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140446151,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs942413015","feature_type":"variation","strand":1,"end":140446153,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446153},{"seq_region_name":"7","id":"rs1207732780","clinical_significance":[],"start":140446155,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","A"],"end":140446155,"strand":1,"feature_type":"variation"},{"alleles":["C","T"],"end":140446157,"feature_type":"variation","strand":1,"source":"dbSNP","start":140446157,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs920686957","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799886419","source":"dbSNP","start":140446157,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["CC","C"],"end":140446158,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140446158,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446158,"source":"dbSNP","id":"rs535087324","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs35019434","clinical_significance":[],"start":140446159,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140446166,"alleles":["AAAAAAAA","AAAAAAA","AAAAAAAAA"],"strand":1,"feature_type":"variation"},{"end":140446163,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140446163,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1311512563"},{"feature_type":"variation","strand":1,"alleles":["AAACAAA","AAA"],"end":140446170,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446164,"clinical_significance":[],"id":"rs2130213044","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs553828048","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446165,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140446165},{"seq_region_name":"7","id":"rs1799886562","clinical_significance":[],"strand":1,"feature_type":"variation","end":140446166,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446166,"source":"dbSNP"},{"clinical_significance":[],"id":"rs2030562","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140446167,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446167},{"clinical_significance":[],"id":"rs200578003","seq_region_name":"7","alleles":["C","-"],"end":140446167,"feature_type":"variation","strand":1,"source":"dbSNP","start":140446167,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs386718463","clinical_significance":[],"start":140446167,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["CA","AC"],"end":140446168,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs6947164","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446168,"source":"dbSNP","strand":1,"feature_type":"variation","end":140446168,"alleles":["A","C"]},{"seq_region_name":"7","id":"rs367597870","clinical_significance":[],"strand":1,"feature_type":"variation","end":140446178,"alleles":["AAAAAAAAAAA","AAA","AAAAAAAAA","AAAAAAAAAA","AAAAAAAAAAAA"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446168,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1491449378","alleles":["-","C"],"end":140446168,"feature_type":"variation","strand":1,"source":"dbSNP","start":140446169,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"start":140446169,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","C"],"end":140446169,"strand":1,"feature_type":"variation","id":"rs1799886837","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140446170,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140446170,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1465896386","seq_region_name":"7"},{"id":"rs1799886874","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446179,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["-","T"],"end":140446178},{"seq_region_name":"7","id":"rs893001264","clinical_significance":[],"start":140446179,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140446179,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1310831245","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A","C","G"],"end":140446180,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446180,"source":"dbSNP"},{"end":140446181,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140446181,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799886943"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446182,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140446182,"seq_region_name":"7","id":"rs1187498398","clinical_significance":[]},{"end":140446193,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140446193,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1585451854","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140446195,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446195,"source":"dbSNP","seq_region_name":"7","id":"rs2130213146","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799887004","alleles":["TCTCACTCAT","T"],"end":140446204,"feature_type":"variation","strand":1,"source":"dbSNP","start":140446195,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799887023","source":"dbSNP","start":140446196,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140446196,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs908065442","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446200,"feature_type":"variation","strand":1,"end":140446200,"alleles":["C","T"]},{"id":"rs1799887061","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446202,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140446202},{"seq_region_name":"7","id":"rs1444833699","clinical_significance":[],"end":140446205,"alleles":["ATT","-"],"strand":1,"feature_type":"variation","start":140446203,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"source":"dbSNP","start":140446205,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140446205,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585451862"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799887109","end":140446214,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140446214,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1799887135","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446222,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140446222},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446223,"feature_type":"variation","strand":1,"end":140446227,"alleles":["GTGGT","GT"],"clinical_significance":[],"seq_region_name":"7","id":"rs1340015687"},{"end":140446225,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140446225,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799887186"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446226,"source":"dbSNP","strand":1,"feature_type":"variation","end":140446226,"alleles":["G","T"],"seq_region_name":"7","id":"rs944864965","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799887238","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446232,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140446232},{"clinical_significance":[],"seq_region_name":"7","id":"rs1257897147","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446234,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140446234},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799887276","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446235,"feature_type":"variation","strand":1,"end":140446235,"alleles":["C","-"]},{"clinical_significance":[],"id":"rs1799887295","seq_region_name":"7","feature_type":"variation","strand":1,"end":140446237,"alleles":["T","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446237},{"feature_type":"variation","strand":1,"end":140446239,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446239,"clinical_significance":[],"seq_region_name":"7","id":"rs1198503152"},{"strand":1,"feature_type":"variation","alleles":["AAAA","AA"],"end":140446244,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446241,"source":"dbSNP","id":"rs777196402","seq_region_name":"7","clinical_significance":[]},{"id":"rs1272480282","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["ACA","A"],"end":140446246,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446244,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1316544133","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446246,"feature_type":"variation","strand":1,"end":140446246,"alleles":["A","C"]},{"alleles":["G","A"],"end":140446247,"strand":1,"feature_type":"variation","start":140446247,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799887433","clinical_significance":[]},{"source":"dbSNP","start":140446248,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140446248,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1207226448","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs765617508","alleles":["TTT","T"],"end":140446250,"feature_type":"variation","strand":1,"source":"dbSNP","start":140446248,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140446249,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446249,"source":"dbSNP","seq_region_name":"7","id":"rs1040668017","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs558092582","feature_type":"variation","strand":1,"end":140446250,"alleles":["T","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446250},{"seq_region_name":"7","id":"rs1297000127","clinical_significance":[],"strand":1,"feature_type":"variation","end":140446251,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446251,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446253,"source":"dbSNP","strand":1,"feature_type":"variation","end":140446253,"alleles":["C","T"],"seq_region_name":"7","id":"rs1246850031","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446255,"feature_type":"variation","strand":1,"end":140446255,"alleles":["G","A"],"clinical_significance":[],"id":"rs1799887592","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140446257,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446257,"source":"dbSNP","seq_region_name":"7","id":"rs1342459840","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563082007","feature_type":"variation","strand":1,"end":140446265,"alleles":["AAAA","AAA"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446262},{"seq_region_name":"7","id":"rs922142011","clinical_significance":[],"start":140446266,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140446266,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799887676","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446267,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140446267},{"clinical_significance":[],"seq_region_name":"7","id":"rs1395744150","alleles":["T","C","G"],"end":140446269,"feature_type":"variation","strand":1,"source":"dbSNP","start":140446269,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1041626867","clinical_significance":[],"start":140446270,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G","T"],"end":140446270,"strand":1,"feature_type":"variation"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446272,"feature_type":"variation","strand":1,"end":140446274,"alleles":["ACA","A"],"clinical_significance":[],"id":"rs1799887748","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140446274,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446274,"clinical_significance":[],"id":"rs907091496","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1585451931","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446277,"feature_type":"variation","strand":1,"end":140446277,"alleles":["T","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799887820","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446278,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140446278},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446279,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140446279,"seq_region_name":"7","id":"rs1002848794","clinical_significance":[]},{"source":"dbSNP","start":140446280,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140446280,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1462389057","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140446281,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446281,"source":"dbSNP","seq_region_name":"7","id":"rs1167394546","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140446282,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446282,"source":"dbSNP","seq_region_name":"7","id":"rs1198434438","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799888119","source":"dbSNP","start":140446284,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140446284,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs931645696","alleles":["G","T"],"end":140446285,"feature_type":"variation","strand":1,"source":"dbSNP","start":140446285,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1369830971","alleles":["CCC","CC"],"end":140446289,"feature_type":"variation","strand":1,"source":"dbSNP","start":140446287,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"id":"rs1799888183","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140446289,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446289,"source":"dbSNP"},{"source":"dbSNP","start":140446290,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140446290,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1255047446","seq_region_name":"7"},{"clinical_significance":[],"id":"rs759449087","seq_region_name":"7","source":"dbSNP","start":140446291,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140446291,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1184962764","clinical_significance":[],"end":140446295,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140446295,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446300,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140446300,"seq_region_name":"7","id":"rs1422964690","clinical_significance":[]},{"start":140446307,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140446307,"alleles":["G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs892801372","clinical_significance":[]},{"clinical_significance":[],"id":"rs1010422840","seq_region_name":"7","end":140446309,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140446309,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1184205707","feature_type":"variation","strand":1,"end":140446309,"alleles":["A","AA"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446309},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799888369","alleles":["C","T"],"end":140446312,"feature_type":"variation","strand":1,"source":"dbSNP","start":140446312,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1273889636","source":"dbSNP","start":140446314,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140446314,"alleles":["C","A","G","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585451972","source":"dbSNP","start":140446318,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140446318,"alleles":["A","G"],"feature_type":"variation","strand":1},{"start":140446330,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","C"],"end":140446330,"strand":1,"feature_type":"variation","id":"rs1799888443","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446333,"feature_type":"variation","strand":1,"end":140446336,"alleles":["ATAT","AT"],"clinical_significance":[],"seq_region_name":"7","id":"rs1034284830"},{"end":140446334,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140446334,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs958722092","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140446337,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446337,"clinical_significance":[],"seq_region_name":"7","id":"rs1799888524"},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140446341,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446341,"clinical_significance":[],"id":"rs1244363147","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1006739833","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446342,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140446342},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446344,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140446344,"seq_region_name":"7","id":"rs188051763","clinical_significance":[]},{"seq_region_name":"7","id":"rs1290567968","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446344,"source":"dbSNP","strand":1,"feature_type":"variation","end":140446344,"alleles":["C","-"]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446350,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140446350,"seq_region_name":"7","id":"rs1799888649","clinical_significance":[]},{"alleles":["C","G"],"end":140446351,"feature_type":"variation","strand":1,"source":"dbSNP","start":140446351,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs576108055","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1350399054","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446353,"feature_type":"variation","strand":1,"end":140446353,"alleles":["G","A"]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446358,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140446358,"clinical_significance":[],"seq_region_name":"7","id":"rs1304354685"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140446360,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446360,"clinical_significance":[],"seq_region_name":"7","id":"rs2130213468"},{"seq_region_name":"7","id":"rs1799888742","clinical_significance":[],"end":140446362,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140446362,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799888761","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446368,"feature_type":"variation","strand":1,"end":140446368,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs543626101","clinical_significance":[],"start":140446370,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140446370,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799888805","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446378,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140446378},{"clinical_significance":[],"seq_region_name":"7","id":"rs1161041420","alleles":["T","G"],"end":140446380,"feature_type":"variation","strand":1,"source":"dbSNP","start":140446380,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs907042828","clinical_significance":[],"start":140446381,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140446381,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140446383,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140446383,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1412308180"},{"source":"dbSNP","start":140446386,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140446386,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1002685894"},{"id":"rs1471519667","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446390,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140446390},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446392,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140446392,"seq_region_name":"7","id":"rs1799888942","clinical_significance":[]},{"clinical_significance":[],"id":"rs767338102","seq_region_name":"7","alleles":["G","A"],"end":140446398,"feature_type":"variation","strand":1,"source":"dbSNP","start":140446398,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1431235577","alleles":["G","A"],"end":140446399,"feature_type":"variation","strand":1,"source":"dbSNP","start":140446399,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1799889025","seq_region_name":"7","source":"dbSNP","start":140446401,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140446401,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140446402,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140446402,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1453352100"},{"source":"dbSNP","start":140446403,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140446403,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799889075"},{"source":"dbSNP","start":140446404,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140446404,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799889092"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1265397994","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446410,"feature_type":"variation","strand":1,"end":140446410,"alleles":["A","G"]},{"source":"dbSNP","start":140446415,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140446415,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1464351691"},{"clinical_significance":[],"seq_region_name":"7","id":"rs923518673","source":"dbSNP","start":140446416,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140446416,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs954916925","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446424,"source":"dbSNP","strand":1,"feature_type":"variation","end":140446424,"alleles":["C","T"]},{"id":"rs1301356274","seq_region_name":"7","clinical_significance":[],"end":140446427,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140446427,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446428,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AA","-"],"end":140446429,"seq_region_name":"7","id":"rs1799889243","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799889266","end":140446429,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140446429,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140446434,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140446434,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1328908511"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1284418753","end":140446442,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140446442,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140446444,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140446444,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799889338","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs371957376","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446447,"feature_type":"variation","strand":1,"end":140446447,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799889381","feature_type":"variation","strand":1,"end":140446449,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446449},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446455,"feature_type":"variation","strand":1,"end":140446455,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799889399"},{"start":140446456,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140446456,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs193033138","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130213594","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446458,"feature_type":"variation","strand":1,"end":140446458,"alleles":["C","T"]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140446461,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446461,"clinical_significance":[],"seq_region_name":"7","id":"rs1799889459"},{"seq_region_name":"7","id":"rs910905670","clinical_significance":[],"start":140446463,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","C","G"],"end":140446463,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs995376195","clinical_significance":[],"alleles":["C","T"],"end":140446469,"strand":1,"feature_type":"variation","start":140446469,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"end":140446470,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140446470,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs10226064"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446479,"feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140446479,"clinical_significance":[],"id":"rs1322209772","seq_region_name":"7"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446481,"feature_type":"variation","strand":1,"end":140446481,"alleles":["T","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1455394449"},{"start":140446484,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140446484,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799889827","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1218504756","alleles":["G","A","C"],"end":140446486,"feature_type":"variation","strand":1,"source":"dbSNP","start":140446486,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446487,"feature_type":"variation","strand":1,"end":140446487,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1284471809"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799889909","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140446488,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446488},{"source":"dbSNP","start":140446493,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140446493,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799889923","seq_region_name":"7"},{"end":140446495,"alleles":["G","A","C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140446495,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs755705580"},{"seq_region_name":"7","id":"rs1799889979","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140446498,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446498,"source":"dbSNP"},{"seq_region_name":"7","id":"rs2130213679","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446503,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140446503},{"feature_type":"variation","strand":1,"end":140446505,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446505,"clinical_significance":[],"id":"rs1054649558","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799890024","clinical_significance":[],"end":140446506,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140446506,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1799890052","clinical_significance":[],"alleles":["A","G"],"end":140446510,"strand":1,"feature_type":"variation","start":140446510,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1326188526","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140446513,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446513,"source":"dbSNP"},{"start":140446514,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140446514,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs983956525","clinical_significance":[]},{"source":"dbSNP","start":140446515,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140446515,"alleles":["A","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs542786347"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446516,"feature_type":"variation","strand":1,"alleles":["TTTTTT","TTTTTTT"],"end":140446521,"clinical_significance":[],"seq_region_name":"7","id":"rs1478951108"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140446524,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446524,"clinical_significance":[],"seq_region_name":"7","id":"rs1799890195"},{"id":"rs10229678","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446525,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140446525},{"alleles":["G","A"],"end":140446526,"strand":1,"feature_type":"variation","start":140446526,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1465456444","seq_region_name":"7","clinical_significance":[]},{"start":140446529,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140446529,"alleles":["C","G"],"strand":1,"feature_type":"variation","id":"rs1799890332","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140446530,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446530,"source":"dbSNP","seq_region_name":"7","id":"rs1207070444","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446530,"source":"dbSNP","strand":1,"feature_type":"variation","end":140446530,"alleles":["A","-"],"seq_region_name":"7","id":"rs1799890375","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1041508500","end":140446531,"alleles":["AG","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140446530,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1464688331","alleles":["GGGGG","GGGG","GGGGGG"],"end":140446535,"feature_type":"variation","strand":1,"source":"dbSNP","start":140446531,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1279815852","clinical_significance":[],"end":140446532,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140446532,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1799890468","clinical_significance":[],"alleles":["G","C"],"end":140446533,"strand":1,"feature_type":"variation","start":140446533,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"id":"rs907142588","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446534,"feature_type":"variation","strand":1,"end":140446534,"alleles":["G","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799890509","feature_type":"variation","strand":1,"end":140446535,"alleles":["G","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446535},{"seq_region_name":"7","id":"rs143656272","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446537,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140446537},{"end":140446538,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140446538,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1274835586"},{"end":140446541,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140446541,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799890595"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446543,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140446543,"clinical_significance":[],"seq_region_name":"7","id":"rs111750723"},{"seq_region_name":"7","id":"rs1585452078","clinical_significance":[],"strand":1,"feature_type":"variation","end":140446544,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446544,"source":"dbSNP"},{"alleles":["T","G"],"end":140446545,"strand":1,"feature_type":"variation","start":140446545,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1585452080","clinical_significance":[]},{"seq_region_name":"7","id":"rs1487667248","clinical_significance":[],"start":140446546,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140446546,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585452088","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140446548,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446548},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446557,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140446557,"clinical_significance":[],"id":"rs1799890730","seq_region_name":"7"},{"end":140446562,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140446562,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799890745"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799890761","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446567,"feature_type":"variation","strand":1,"end":140446567,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1799890788","clinical_significance":[],"strand":1,"feature_type":"variation","end":140446570,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446570,"source":"dbSNP"},{"start":140446571,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140446571,"strand":1,"feature_type":"variation","id":"rs894506028","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799890838","seq_region_name":"7","end":140446572,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140446572,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446575,"source":"dbSNP","strand":1,"feature_type":"variation","end":140446575,"alleles":["T","C"],"seq_region_name":"7","id":"rs1799890862","clinical_significance":[]},{"seq_region_name":"7","id":"rs922089335","clinical_significance":[],"alleles":["G","A"],"end":140446577,"strand":1,"feature_type":"variation","start":140446577,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"alleles":["G","A"],"end":140446578,"strand":1,"feature_type":"variation","start":140446578,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1299296848","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140446588,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446588,"source":"dbSNP","seq_region_name":"7","id":"rs1432490797","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1387504315","end":140446591,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140446591,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1006213415","clinical_significance":[],"start":140446593,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["AA","A"],"end":140446594,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140446599,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446599,"source":"dbSNP","seq_region_name":"7","id":"rs185194926","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs78222696","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446600,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140446600},{"end":140446601,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140446601,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799891317","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs993682785","source":"dbSNP","start":140446602,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140446602,"alleles":["G","A"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140446606,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446606,"source":"dbSNP","seq_region_name":"7","id":"rs914249901","clinical_significance":[]},{"seq_region_name":"7","id":"rs945701451","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446607,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","G","T"],"end":140446607},{"id":"rs1030473687","seq_region_name":"7","clinical_significance":[],"start":140446608,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140446608,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1041875450","clinical_significance":[],"start":140446614,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140446614,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1585452130","seq_region_name":"7","end":140446616,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140446616,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1186863619","end":140446617,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140446617,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1449052299","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446618,"feature_type":"variation","strand":1,"end":140446618,"alleles":["G","A"]},{"feature_type":"variation","strand":1,"end":140446621,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446621,"clinical_significance":[],"id":"rs954843656","seq_region_name":"7"},{"seq_region_name":"7","id":"rs139602739","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446622,"source":"dbSNP","strand":1,"feature_type":"variation","end":140446622,"alleles":["G","A","C"]},{"start":140446633,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140446633,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs906911001","clinical_significance":[]},{"start":140446634,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","T"],"end":140446634,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1206532054","clinical_significance":[]},{"seq_region_name":"7","id":"rs1017850755","clinical_significance":[],"alleles":["G","A"],"end":140446637,"strand":1,"feature_type":"variation","start":140446637,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446638,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140446638,"seq_region_name":"7","id":"rs189321695","clinical_significance":[]},{"start":140446639,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140446639,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799891674","clinical_significance":[]},{"start":140446640,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140446640,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs568038334","clinical_significance":[]},{"clinical_significance":[],"id":"rs746385531","seq_region_name":"7","alleles":["C","A","G","T"],"end":140446641,"feature_type":"variation","strand":1,"source":"dbSNP","start":140446641,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446642,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140446642,"clinical_significance":[],"id":"rs758836140","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446644,"source":"dbSNP","strand":1,"feature_type":"variation","end":140446644,"alleles":["A","G"],"seq_region_name":"7","id":"rs1799891815","clinical_significance":[]},{"id":"rs1799891841","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446646,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140446646},{"seq_region_name":"7","id":"rs75527612","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446652,"source":"dbSNP","strand":1,"feature_type":"variation","end":140446652,"alleles":["T","G"]},{"alleles":["T","C"],"end":140446654,"feature_type":"variation","strand":1,"source":"dbSNP","start":140446654,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799891906"},{"source":"dbSNP","start":140446657,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140446657,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1333372836"},{"strand":1,"feature_type":"variation","end":140446658,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446658,"source":"dbSNP","seq_region_name":"7","id":"rs1799891934","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446663,"feature_type":"variation","strand":1,"end":140446663,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799891955"},{"id":"rs1799891979","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140446665,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446665,"source":"dbSNP"},{"id":"rs1799891999","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446668,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140446668},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130214045","end":140446672,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140446672,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1385479924","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446676,"feature_type":"variation","strand":1,"end":140446676,"alleles":["A","T"]},{"seq_region_name":"7","id":"rs1799892051","clinical_significance":[],"end":140446683,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140446683,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"feature_type":"variation","strand":1,"end":140446684,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446684,"clinical_significance":[],"seq_region_name":"7","id":"rs576336206"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799892112","end":140446689,"alleles":["TT","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140446688,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140446692,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446692,"clinical_significance":[],"id":"rs1335992575","seq_region_name":"7"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446693,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140446693,"clinical_significance":[],"seq_region_name":"7","id":"rs1241940767"},{"start":140446694,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140446694,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1004847997","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446695,"feature_type":"variation","strand":1,"end":140446695,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs553793196"},{"source":"dbSNP","start":140446698,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140446698,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs768956429"},{"seq_region_name":"7","id":"rs1183820840","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446701,"source":"dbSNP","strand":1,"feature_type":"variation","end":140446701,"alleles":["A","C"]},{"seq_region_name":"7","id":"rs1799892437","clinical_significance":[],"alleles":["C","T"],"end":140446702,"strand":1,"feature_type":"variation","start":140446702,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446705,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140446705,"seq_region_name":"7","id":"rs1799892456","clinical_significance":[]},{"source":"dbSNP","start":140446708,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140446708,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799892479"},{"clinical_significance":[],"seq_region_name":"7","id":"rs75927059","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446710,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140446710},{"end":140446711,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140446711,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1029186791","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1352388371","end":140446716,"alleles":["GCCCG","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140446712,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs942028079","feature_type":"variation","strand":1,"end":140446713,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446713},{"seq_region_name":"7","id":"rs953514933","clinical_significance":[],"alleles":["C","A"],"end":140446714,"strand":1,"feature_type":"variation","start":140446714,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140446715,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446715,"clinical_significance":[],"seq_region_name":"7","id":"rs1799892648"},{"start":140446716,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140446716,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs1222568583","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140446717,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140446717,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1202407512","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1227614999","clinical_significance":[],"end":140446726,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140446726,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"source":"dbSNP","start":140446728,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140446728,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1037682276"},{"strand":1,"feature_type":"variation","end":140446729,"alleles":["C","A","G","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446729,"source":"dbSNP","seq_region_name":"7","id":"rs1585452207","clinical_significance":[]},{"seq_region_name":"7","id":"rs61448912","clinical_significance":[],"start":140446729,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140446730,"alleles":["CC","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs539443035","clinical_significance":[],"strand":1,"feature_type":"variation","end":140446732,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446732,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1190438377","seq_region_name":"7","source":"dbSNP","start":140446733,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140446733,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140446736,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446736,"clinical_significance":[],"seq_region_name":"7","id":"rs1799893316"},{"clinical_significance":[],"seq_region_name":"7","id":"rs748365283","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446740,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140446740},{"source":"dbSNP","start":140446742,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140446742,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1030399989"},{"alleles":["C","T"],"end":140446744,"strand":1,"feature_type":"variation","start":140446744,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs369762195","clinical_significance":[]},{"id":"rs28785875","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140446745,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446745,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799893500","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446750,"feature_type":"variation","strand":1,"end":140446750,"alleles":["G","A"]},{"clinical_significance":[],"id":"rs1799893527","seq_region_name":"7","source":"dbSNP","start":140446755,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140446755,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140446756,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446756,"clinical_significance":[],"seq_region_name":"7","id":"rs28824916"},{"strand":1,"feature_type":"variation","end":140446758,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446758,"source":"dbSNP","id":"rs1799893597","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs779672781","clinical_significance":[],"end":140446762,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140446762,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"source":"dbSNP","start":140446763,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140446763,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1018277855"},{"seq_region_name":"7","id":"rs377710652","clinical_significance":[],"start":140446764,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140446764,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs28832645","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446765,"feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140446765},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446767,"feature_type":"variation","strand":1,"end":140446767,"alleles":["C","T"],"clinical_significance":[],"id":"rs759450550","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1799893816","seq_region_name":"7","end":140446768,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140446768,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1799893841","clinical_significance":[],"start":140446770,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","C"],"end":140446770,"strand":1,"feature_type":"variation"},{"alleles":["GGG","GG"],"end":140446772,"strand":1,"feature_type":"variation","start":140446770,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799893852","clinical_significance":[]},{"alleles":["G","A"],"end":140446772,"strand":1,"feature_type":"variation","start":140446772,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1413407641","clinical_significance":[]},{"end":140446773,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140446773,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1585452263","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799893907","clinical_significance":[],"start":140446779,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","T"],"end":140446779,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1799893932","seq_region_name":"7","source":"dbSNP","start":140446780,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140446780,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140446781,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446781,"source":"dbSNP","seq_region_name":"7","id":"rs1799893949","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1160352017","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446782,"feature_type":"variation","strand":1,"end":140446782,"alleles":["C","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799893983","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446783,"feature_type":"variation","strand":1,"end":140446783,"alleles":["C","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799894000","source":"dbSNP","start":140446793,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140446793,"alleles":["A","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs2130214309","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140446796,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446796},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446798,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140446798,"clinical_significance":[],"seq_region_name":"7","id":"rs1293437515"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446799,"feature_type":"variation","strand":1,"end":140446799,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs938473821"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446800,"feature_type":"variation","strand":1,"end":140446800,"alleles":["C","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799894078"},{"end":140446801,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140446801,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799894101"},{"clinical_significance":[],"seq_region_name":"7","id":"rs768418306","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446807,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140446807},{"end":140446809,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140446809,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799894165","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446821,"feature_type":"variation","strand":1,"end":140446821,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1473816834"},{"seq_region_name":"7","id":"rs574049815","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140446823,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446823,"source":"dbSNP"},{"alleles":["T","G"],"end":140446825,"feature_type":"variation","strand":1,"source":"dbSNP","start":140446825,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs115283469"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140446828,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446828,"source":"dbSNP","seq_region_name":"7","id":"rs1306703126","clinical_significance":[]},{"end":140446833,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140446833,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799894354","clinical_significance":[]},{"alleles":["T","A"],"end":140446835,"strand":1,"feature_type":"variation","start":140446835,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs977180854","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140446836,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446836,"clinical_significance":[],"seq_region_name":"7","id":"rs1799894407"},{"id":"rs1799894433","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140446840,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446840,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1246812566","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140446843,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446843},{"id":"rs1799894486","seq_region_name":"7","clinical_significance":[],"end":140446844,"alleles":["GG","G"],"strand":1,"feature_type":"variation","start":140446843,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"end":140446857,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140446857,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs928379502","clinical_significance":[]},{"id":"rs1449488771","seq_region_name":"7","clinical_significance":[],"start":140446858,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140446858,"alleles":["A","G","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1223178924","clinical_significance":[],"alleles":["ATTAT","AT"],"end":140446862,"strand":1,"feature_type":"variation","start":140446858,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"id":"rs1272212979","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140446862,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446862,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1228774551","end":140446864,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140446864,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140446865,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446865,"source":"dbSNP","seq_region_name":"7","id":"rs1799894611","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446867,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140446867,"clinical_significance":[],"seq_region_name":"7","id":"rs1330955760"},{"start":140446868,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140446868,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799894651","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs775215744","alleles":["C","A"],"end":140446870,"feature_type":"variation","strand":1,"source":"dbSNP","start":140446870,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799894697","source":"dbSNP","start":140446889,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140446889,"alleles":["A","C"],"feature_type":"variation","strand":1},{"alleles":["A","G"],"end":140446890,"feature_type":"variation","strand":1,"source":"dbSNP","start":140446890,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs894325200"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446891,"feature_type":"variation","strand":1,"end":140446891,"alleles":["G","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130214457"},{"feature_type":"variation","strand":1,"end":140446893,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446893,"clinical_significance":[],"seq_region_name":"7","id":"rs931124760"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446894,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140446894,"seq_region_name":"7","id":"rs10270875","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446896,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140446896,"seq_region_name":"7","id":"rs1319876565","clinical_significance":[]},{"source":"dbSNP","start":140446898,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140446898,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799895268"},{"seq_region_name":"7","id":"rs1799895292","clinical_significance":[],"start":140446899,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","G"],"end":140446899,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs991298165","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446900,"feature_type":"variation","strand":1,"end":140446900,"alleles":["T","G"]},{"seq_region_name":"7","id":"rs1799895334","clinical_significance":[],"start":140446901,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140446901,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446909,"source":"dbSNP","strand":1,"feature_type":"variation","end":140446909,"alleles":["C","T"],"seq_region_name":"7","id":"rs886994394","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446909,"feature_type":"variation","strand":1,"end":140446910,"alleles":["CC","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs764446361"},{"alleles":["A","C"],"end":140446911,"strand":1,"feature_type":"variation","start":140446911,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1004527354","clinical_significance":[]},{"alleles":["T","A","C"],"end":140446918,"strand":1,"feature_type":"variation","start":140446918,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1196508876","clinical_significance":[]},{"end":140446919,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140446919,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799895458"},{"end":140446922,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140446922,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1459104069"},{"seq_region_name":"7","id":"rs1014963697","clinical_significance":[],"start":140446923,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140446923,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1410248560","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140446924,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446924},{"seq_region_name":"7","id":"rs763926193","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446925,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140446925},{"seq_region_name":"7","id":"rs1236591654","clinical_significance":[],"alleles":["A","G"],"end":140446928,"strand":1,"feature_type":"variation","start":140446928,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446929,"source":"dbSNP","strand":1,"feature_type":"variation","end":140446929,"alleles":["G","A"],"seq_region_name":"7","id":"rs2130214563","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs901825116","end":140446932,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140446932,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs919279979","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446935,"source":"dbSNP","strand":1,"feature_type":"variation","end":140446935,"alleles":["G","A"]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140446936,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446936,"clinical_significance":[],"seq_region_name":"7","id":"rs1427922664"},{"end":140446938,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140446938,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130214582"},{"end":140446946,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140446946,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799895624","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446948,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140446948,"seq_region_name":"7","id":"rs1799895645","clinical_significance":[]},{"id":"rs1585452381","seq_region_name":"7","clinical_significance":[],"start":140446949,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["AGAAATCCTGTCTCTATGGAGTAGTAG","AGAAATCCTGTCTCTATGGAGTAGTAGAAATCCTGTCTCTATGGAGTAGTAG"],"end":140446975,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1439277502","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140446960,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446960,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140446964,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140446964,"clinical_significance":[],"seq_region_name":"7","id":"rs997631722"},{"alleles":["-","A"],"end":140446965,"feature_type":"variation","strand":1,"source":"dbSNP","start":140446966,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1416118176"},{"end":140446967,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140446967,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1051859373","seq_region_name":"7"},{"start":140446968,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","C"],"end":140446968,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1029055810","clinical_significance":[]},{"seq_region_name":"7","id":"rs1422103385","clinical_significance":[],"end":140446969,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140446969,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446970,"source":"dbSNP","strand":1,"feature_type":"variation","end":140446970,"alleles":["T","C"],"seq_region_name":"7","id":"rs890507118","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs533111464","end":140446975,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140446975,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446977,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140446977,"id":"rs990279405","seq_region_name":"7","clinical_significance":[]},{"end":140446978,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140446978,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs893954912","seq_region_name":"7","clinical_significance":[]},{"end":140446980,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140446980,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799895893","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585452410","clinical_significance":[],"start":140446982,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","A","C","G"],"end":140446982,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs76501180","seq_region_name":"7","end":140446983,"alleles":["TT","T","TTT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140446982,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"alleles":["A","G"],"end":140446984,"feature_type":"variation","strand":1,"source":"dbSNP","start":140446984,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799895999"},{"seq_region_name":"7","id":"rs1799896025","clinical_significance":[],"end":140446988,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140446988,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799896048","source":"dbSNP","start":140446991,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140446991,"feature_type":"variation","strand":1},{"end":140446992,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140446992,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1217483431"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140446997,"source":"dbSNP","strand":1,"feature_type":"variation","end":140446997,"alleles":["G","A"],"seq_region_name":"7","id":"rs1799896084","clinical_significance":[]},{"start":140446998,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","C","T"],"end":140446998,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1022303760","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130214689","clinical_significance":[],"end":140446999,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140446999,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"id":"rs1399132333","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447000,"feature_type":"variation","strand":1,"end":140447000,"alleles":["T","C"]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140447003,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447003,"clinical_significance":[],"id":"rs1799896150","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140447004,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447004,"clinical_significance":[],"seq_region_name":"7","id":"rs1437589656"},{"id":"rs1799896180","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447009,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AGAGA","AGA"],"end":140447013},{"clinical_significance":[],"id":"rs1799896202","seq_region_name":"7","source":"dbSNP","start":140447012,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140447012,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140447016,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447016,"clinical_significance":[],"seq_region_name":"7","id":"rs1799896223"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447017,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140447017,"seq_region_name":"7","id":"rs2130214718","clinical_significance":[]},{"source":"dbSNP","start":140447019,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140447019,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1386773840","seq_region_name":"7"},{"end":140447022,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140447022,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1792219354"},{"id":"rs1799896255","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447025,"source":"dbSNP","strand":1,"feature_type":"variation","end":140447025,"alleles":["A","G"]},{"feature_type":"variation","strand":1,"end":140447031,"alleles":["C","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447031,"clinical_significance":[],"seq_region_name":"7","id":"rs2130214725"},{"clinical_significance":[],"id":"rs1799896279","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447032,"feature_type":"variation","strand":1,"end":140447032,"alleles":["A","G"]},{"start":140447033,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140447033,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799896298","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585452430","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447036,"feature_type":"variation","strand":1,"end":140447036,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799896330","source":"dbSNP","start":140447036,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140447039,"alleles":["GTGT","GTGTGT"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140447037,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140447037,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1021623087","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1452848847","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140447038,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447038,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140447043,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447043,"clinical_significance":[],"id":"rs1799896395","seq_region_name":"7"},{"alleles":["T","G"],"end":140447046,"strand":1,"feature_type":"variation","start":140447046,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799896417","clinical_significance":[]},{"source":"dbSNP","start":140447049,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140447049,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs148510025"},{"clinical_significance":[],"id":"rs753478125","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","C","T"],"end":140447051,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447051},{"strand":1,"feature_type":"variation","end":140447056,"alleles":["GGGGGG","GGGGG"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447051,"source":"dbSNP","id":"rs1799896484","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs998442760","end":140447052,"alleles":["G","C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140447052,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447054,"feature_type":"variation","strand":1,"end":140447054,"alleles":["G","C"],"clinical_significance":[],"id":"rs1393978767","seq_region_name":"7"},{"start":140447056,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140447056,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1188756635","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563082234","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447064,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140447064},{"id":"rs1799896589","seq_region_name":"7","clinical_significance":[],"start":140447068,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140447068,"alleles":["A","C","G"],"strand":1,"feature_type":"variation"},{"id":"rs1450921877","seq_region_name":"7","clinical_significance":[],"end":140447070,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140447070,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs928349808","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447071,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140447071},{"clinical_significance":[],"id":"rs1799896883","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447073,"feature_type":"variation","strand":1,"end":140447095,"alleles":["CTCAACTTAGTGGTGAGTATTGC","C"]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447076,"source":"dbSNP","strand":1,"feature_type":"variation","end":140447076,"alleles":["A","G"],"id":"rs1185710726","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs563810384","clinical_significance":[],"strand":1,"feature_type":"variation","end":140447078,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447078,"source":"dbSNP"},{"id":"rs1799896960","seq_region_name":"7","clinical_significance":[],"start":140447080,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140447080,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"end":140447082,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140447082,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1257635432"},{"id":"rs531260824","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140447083,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447083,"source":"dbSNP"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447087,"feature_type":"variation","strand":1,"end":140447087,"alleles":["G","A"],"clinical_significance":[],"id":"rs1207967355","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799897042","clinical_significance":[],"start":140447089,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","C"],"end":140447089,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1347196088","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447092,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140447092},{"alleles":["G","A"],"end":140447094,"feature_type":"variation","strand":1,"source":"dbSNP","start":140447094,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799897077"},{"start":140447096,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140447096,"alleles":["A","-"],"strand":1,"feature_type":"variation","id":"rs1275401737","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140447099,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["CTCT","CT"],"end":140447102,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1319831337"},{"seq_region_name":"7","id":"rs1799897138","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447101,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140447101},{"alleles":["TTTTT","TTT"],"end":140447106,"strand":1,"feature_type":"variation","start":140447102,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1035402950","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799897169","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447103,"feature_type":"variation","strand":1,"alleles":["TTTTCTTTT","TTTT"],"end":140447111},{"feature_type":"variation","strand":1,"end":140447110,"alleles":["TTTCTTT","TTTCTTTCTTT"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447104,"clinical_significance":[],"id":"rs1295203913","seq_region_name":"7"},{"start":140447107,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140447107,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs959758598","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799897223","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447107,"feature_type":"variation","strand":1,"alleles":["CTTTTG","-"],"end":140447112},{"seq_region_name":"7","id":"rs1301551280","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["TTTT","TT"],"end":140447111,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447108,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140447126,"alleles":["TTTTGTTTTGTTTTGTTTT","TTTTGTTTTGTTTT","TTTTGTTTTGTTTTGTTTTGTTTT"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447108,"clinical_significance":[],"seq_region_name":"7","id":"rs991742197"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140447111,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447111,"source":"dbSNP","seq_region_name":"7","id":"rs1371769864","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585452488","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447112,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140447112},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799897317","end":140447115,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140447115,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799897334","feature_type":"variation","strand":1,"end":140447117,"alleles":["G","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447117},{"feature_type":"variation","strand":1,"end":140447121,"alleles":["TTTT","TT","TTT"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447118,"clinical_significance":[],"id":"rs915772436","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799897385","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447122,"source":"dbSNP","strand":1,"feature_type":"variation","end":140447122,"alleles":["G","-"]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447123,"feature_type":"variation","strand":1,"end":140447127,"alleles":["TTTTT","TTTTTT"],"clinical_significance":[],"seq_region_name":"7","id":"rs1431174383"},{"seq_region_name":"7","id":"rs963524631","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140447126,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447126,"source":"dbSNP"},{"source":"dbSNP","start":140447128,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140447128,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1424130841"},{"source":"dbSNP","start":140447132,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140447132,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs756927695","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs549304630","end":140447133,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140447133,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140447137,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140447137,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799897528"},{"strand":1,"feature_type":"variation","end":140447138,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447138,"source":"dbSNP","seq_region_name":"7","id":"rs1799897545","clinical_significance":[]},{"alleles":["C","A"],"end":140447139,"feature_type":"variation","strand":1,"source":"dbSNP","start":140447139,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs919143065"},{"seq_region_name":"7","id":"rs1799897596","clinical_significance":[],"start":140447140,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140447143,"alleles":["AGAG","AG"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1252520126","feature_type":"variation","strand":1,"end":140447144,"alleles":["T","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447144},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447149,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140447149,"clinical_significance":[],"id":"rs1799897617","seq_region_name":"7"},{"start":140447150,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140447150,"strand":1,"feature_type":"variation","id":"rs915621375","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs929295989","source":"dbSNP","start":140447152,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["TT","-"],"end":140447153,"feature_type":"variation","strand":1},{"alleles":["G","C"],"end":140447154,"feature_type":"variation","strand":1,"source":"dbSNP","start":140447154,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs931154443","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1340139238","clinical_significance":[],"start":140447156,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140447156,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs764740182","seq_region_name":"7","source":"dbSNP","start":140447159,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140447159,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1461588721","clinical_significance":[],"start":140447166,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140447167,"alleles":["GG","GGG"],"strand":1,"feature_type":"variation"},{"alleles":["G","T"],"end":140447167,"strand":1,"feature_type":"variation","start":140447167,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1211138826","clinical_significance":[]},{"seq_region_name":"7","id":"rs1051746701","clinical_significance":[],"end":140447170,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140447170,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1799897809","clinical_significance":[],"alleles":["A","G"],"end":140447174,"strand":1,"feature_type":"variation","start":140447174,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1310986801","source":"dbSNP","start":140447175,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140447175,"alleles":["T","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1414615789","end":140447179,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140447179,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"alleles":["C","T"],"end":140447180,"strand":1,"feature_type":"variation","start":140447180,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1482351964","clinical_significance":[]},{"alleles":["G","A","T"],"end":140447181,"strand":1,"feature_type":"variation","start":140447181,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs749918751","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","T"],"end":140447184,"feature_type":"variation","strand":1,"source":"dbSNP","start":140447184,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs908367382"},{"clinical_significance":[],"seq_region_name":"7","id":"rs567889481","source":"dbSNP","start":140447186,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140447186,"alleles":["C","G","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1041349197","alleles":["G","A"],"end":140447187,"feature_type":"variation","strand":1,"source":"dbSNP","start":140447187,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447192,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140447192,"id":"rs1166922669","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140447194,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447194,"clinical_significance":[],"seq_region_name":"7","id":"rs901860138"},{"clinical_significance":[],"seq_region_name":"7","id":"rs758893240","feature_type":"variation","strand":1,"end":140447195,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447195},{"start":140447196,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140447196,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799898111","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs556003843","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447198,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140447198},{"clinical_significance":[],"seq_region_name":"7","id":"rs144292518","feature_type":"variation","strand":1,"end":140447201,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447201},{"end":140447205,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140447205,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs548032515"},{"alleles":["C","T"],"end":140447208,"feature_type":"variation","strand":1,"source":"dbSNP","start":140447208,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs182002005","seq_region_name":"7"},{"start":140447209,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140447209,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs747554357","clinical_significance":[]},{"id":"rs1479065895","seq_region_name":"7","clinical_significance":[],"start":140447210,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140447210,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447211,"source":"dbSNP","strand":1,"feature_type":"variation","end":140447211,"alleles":["G","A"],"seq_region_name":"7","id":"rs943495655","clinical_significance":[]},{"seq_region_name":"7","id":"rs1012067058","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447212,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140447212},{"seq_region_name":"7","id":"rs1249948438","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140447213,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447213,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1423412901","seq_region_name":"7","alleles":["C","G"],"end":140447216,"feature_type":"variation","strand":1,"source":"dbSNP","start":140447216,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140447217,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["AA","-"],"end":140447218,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799898358","seq_region_name":"7"},{"id":"rs894014692","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140447218,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447218,"source":"dbSNP"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447220,"feature_type":"variation","strand":1,"end":140447220,"alleles":["A","C"],"clinical_significance":[],"id":"rs1799898401","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447226,"source":"dbSNP","strand":1,"feature_type":"variation","end":140447226,"alleles":["T","A"],"seq_region_name":"7","id":"rs1799898420","clinical_significance":[]},{"clinical_significance":[],"id":"rs1263969690","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447234,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140447234},{"seq_region_name":"7","id":"rs146586647","clinical_significance":[],"start":140447241,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140447241,"strand":1,"feature_type":"variation"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447246,"feature_type":"variation","strand":1,"end":140447245,"alleles":["-","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799898479"},{"clinical_significance":[],"id":"rs1799898495","seq_region_name":"7","feature_type":"variation","strand":1,"end":140447249,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447249},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140447250,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447250,"source":"dbSNP","seq_region_name":"7","id":"rs1799898520","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447257,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140447257,"clinical_significance":[],"seq_region_name":"7","id":"rs1330260201"},{"start":140447261,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","A"],"end":140447261,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1290705088","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799898587","clinical_significance":[],"end":140447262,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140447262,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1042626088","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447263,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140447263},{"start":140447265,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","A","T"],"end":140447265,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs183569647","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140447266,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447266,"source":"dbSNP","seq_region_name":"7","id":"rs1335851594","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799898686","feature_type":"variation","strand":1,"end":140447268,"alleles":["T","C","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447268},{"start":140447273,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","A","T"],"end":140447273,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs140121976","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs776803755","source":"dbSNP","start":140447274,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140447274,"feature_type":"variation","strand":1},{"alleles":["C","A"],"end":140447276,"feature_type":"variation","strand":1,"source":"dbSNP","start":140447276,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799898776","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140447277,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447277,"clinical_significance":[],"id":"rs1799898798","seq_region_name":"7"},{"source":"dbSNP","start":140447278,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140447278,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130215170"},{"seq_region_name":"7","id":"rs1323481669","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447283,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140447283},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447284,"source":"dbSNP","strand":1,"feature_type":"variation","end":140447284,"alleles":["T","C"],"seq_region_name":"7","id":"rs1799898833","clinical_significance":[]},{"clinical_significance":[],"id":"rs999130155","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140447287,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447287},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140447290,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447290,"clinical_significance":[],"seq_region_name":"7","id":"rs1799898882"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799898908","feature_type":"variation","strand":1,"end":140447295,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447295},{"seq_region_name":"7","id":"rs1412463987","clinical_significance":[],"start":140447296,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140447296,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1161231856","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140447299,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447299},{"seq_region_name":"7","id":"rs1799898956","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447300,"source":"dbSNP","strand":1,"feature_type":"variation","end":140447300,"alleles":["A","G"]},{"start":140447301,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140447301,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs959958722","clinical_significance":[]},{"end":140447302,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140447302,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1012689327"},{"start":140447304,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140447304,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799899033","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140447307,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447307,"source":"dbSNP","seq_region_name":"7","id":"rs1036329374","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447308,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140447308,"clinical_significance":[],"seq_region_name":"7","id":"rs1799899068"},{"source":"dbSNP","start":140447309,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140447309,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799899085","seq_region_name":"7"},{"alleles":["TTT","TT"],"end":140447312,"feature_type":"variation","strand":1,"source":"dbSNP","start":140447310,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1251313228"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447317,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140447317,"clinical_significance":[],"seq_region_name":"7","id":"rs1213329053"},{"seq_region_name":"7","id":"rs1799899143","clinical_significance":[],"end":140447318,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140447318,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1446665214","source":"dbSNP","start":140447322,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140447322,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799899183","alleles":["G","C"],"end":140447327,"feature_type":"variation","strand":1,"source":"dbSNP","start":140447327,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799899212","feature_type":"variation","strand":1,"end":140447328,"alleles":["G","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447328},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140447331,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447331,"clinical_significance":[],"seq_region_name":"7","id":"rs963274158"},{"clinical_significance":[],"seq_region_name":"7","id":"rs973607301","source":"dbSNP","start":140447332,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140447332,"alleles":["G","A","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs781726453","clinical_significance":[],"end":140447336,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140447336,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"id":"rs991080261","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447337,"feature_type":"variation","strand":1,"end":140447337,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs915568930","source":"dbSNP","start":140447344,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140447344,"alleles":["T","C"],"feature_type":"variation","strand":1},{"id":"rs952501290","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447347,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140447347},{"seq_region_name":"7","id":"rs950587833","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447348,"source":"dbSNP","strand":1,"feature_type":"variation","end":140447348,"alleles":["C","T"]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447353,"feature_type":"variation","strand":1,"end":140447353,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799899369"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447354,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140447354,"seq_region_name":"7","id":"rs1300740300","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447356,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140447356,"seq_region_name":"7","id":"rs188257111","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799899439","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447359,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140447359},{"seq_region_name":"7","id":"rs908402262","clinical_significance":[],"start":140447360,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140447360,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1388974054","clinical_significance":[],"alleles":["C","T"],"end":140447362,"strand":1,"feature_type":"variation","start":140447362,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs911920556","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447364,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140447364},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447368,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140447368,"seq_region_name":"7","id":"rs943363427","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447369,"feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140447369,"clinical_significance":[],"id":"rs939823433","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1209547261","source":"dbSNP","start":140447379,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140447379,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140447380,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140447379,"alleles":["-","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1393385645"},{"strand":1,"feature_type":"variation","end":140447380,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447380,"source":"dbSNP","seq_region_name":"7","id":"rs1193134457","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["GT","-"],"end":140447381,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447380,"source":"dbSNP","seq_region_name":"7","id":"rs1799899610","clinical_significance":[]},{"id":"rs1450304970","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447381,"source":"dbSNP","strand":1,"feature_type":"variation","end":140447382,"alleles":["TA","-"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs946906364","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447382,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140447382},{"seq_region_name":"7","id":"rs1191475913","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447383,"source":"dbSNP","strand":1,"feature_type":"variation","end":140447383,"alleles":["C","T"]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447387,"feature_type":"variation","strand":1,"end":140447387,"alleles":["G","A","C"],"clinical_significance":[],"id":"rs1799899681","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1446787391","clinical_significance":[],"strand":1,"feature_type":"variation","end":140447389,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447389,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140447392,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447392,"source":"dbSNP","seq_region_name":"7","id":"rs1799899705","clinical_significance":[]},{"start":140447396,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140447396,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs143764473","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs373907842","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447397,"feature_type":"variation","strand":1,"end":140447397,"alleles":["G","A","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799899765","end":140447398,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140447398,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"alleles":["A","C"],"end":140447400,"strand":1,"feature_type":"variation","start":140447400,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1585452701","clinical_significance":[]},{"alleles":["A","C","G"],"end":140447404,"strand":1,"feature_type":"variation","start":140447404,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs933316506","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585452702","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447406,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140447406},{"seq_region_name":"7","id":"rs1799899841","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140447407,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447407,"source":"dbSNP"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447409,"feature_type":"variation","strand":1,"end":140447409,"alleles":["A","C"],"clinical_significance":[],"id":"rs1585452711","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799899875","clinical_significance":[],"alleles":["C","A","T"],"end":140447412,"strand":1,"feature_type":"variation","start":140447412,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447413,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140447413,"seq_region_name":"7","id":"rs1056621608","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799899919","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447415,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","G","T"],"end":140447415},{"seq_region_name":"7","id":"rs1263093433","clinical_significance":[],"alleles":["TGTTGTT","TGTT"],"end":140447423,"strand":1,"feature_type":"variation","start":140447417,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"alleles":["T","C"],"end":140447419,"feature_type":"variation","strand":1,"source":"dbSNP","start":140447419,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs895521007","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1478592453","source":"dbSNP","start":140447419,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["TT","TTT"],"end":140447420,"feature_type":"variation","strand":1},{"alleles":["TGT","T"],"end":140447422,"feature_type":"variation","strand":1,"source":"dbSNP","start":140447420,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1697733932"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447421,"feature_type":"variation","strand":1,"end":140447421,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1012988211"},{"source":"dbSNP","start":140447421,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140447421,"alleles":["G","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799900033"},{"seq_region_name":"7","id":"rs1392179686","clinical_significance":[],"strand":1,"feature_type":"variation","end":140447422,"alleles":["T","C","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447422,"source":"dbSNP"},{"clinical_significance":[],"id":"rs3042404","seq_region_name":"7","feature_type":"variation","strand":1,"end":140447432,"alleles":["TTTTTTTTTTT","TTTTT","TTTTTTTTT","TTTTTTTTTT","TTTTTTTTTTTT","TTTTTTTTTTTTTT"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447422},{"clinical_significance":[],"seq_region_name":"7","id":"rs1475261048","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447423,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140447423},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447424,"source":"dbSNP","strand":1,"feature_type":"variation","end":140447423,"alleles":["-","G"],"seq_region_name":"7","id":"rs1799900228","clinical_significance":[]},{"seq_region_name":"7","id":"rs1022717379","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140447424,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447424,"source":"dbSNP"},{"id":"rs1190093876","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447428,"source":"dbSNP","strand":1,"feature_type":"variation","end":140447428,"alleles":["T","A"]},{"seq_region_name":"7","id":"rs1212446359","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140447431,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447431,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447432,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TGA","-"],"end":140447434,"seq_region_name":"7","id":"rs1484964452","clinical_significance":[]},{"start":140447437,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140447437,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs1174614095","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs180918906","clinical_significance":[],"start":140447439,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140447439,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140447446,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447446,"source":"dbSNP","seq_region_name":"7","id":"rs1585452774","clinical_significance":[]},{"seq_region_name":"7","id":"rs1413508651","clinical_significance":[],"alleles":["C","T"],"end":140447447,"strand":1,"feature_type":"variation","start":140447447,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"id":"rs1342273520","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140447448,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447448,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["T","-"],"end":140447448,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447448,"source":"dbSNP","seq_region_name":"7","id":"rs1799900373","clinical_significance":[]},{"seq_region_name":"7","id":"rs1274617841","clinical_significance":[],"strand":1,"feature_type":"variation","end":140447449,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447449,"source":"dbSNP"},{"start":140447450,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140447450,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs1799900411","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1159355840","source":"dbSNP","start":140447451,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140447451,"feature_type":"variation","strand":1},{"start":140447455,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140447455,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs759639113","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1050451920","source":"dbSNP","start":140447466,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140447466,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140447467,"alleles":["T","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447467,"clinical_significance":[],"seq_region_name":"7","id":"rs1417317092"},{"seq_region_name":"7","id":"rs889118292","clinical_significance":[],"start":140447470,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140447470,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1340632012","clinical_significance":[],"start":140447471,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140447471,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585452785","source":"dbSNP","start":140447472,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140447472,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1346009018","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447474,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140447474},{"alleles":["C","T"],"end":140447477,"feature_type":"variation","strand":1,"source":"dbSNP","start":140447477,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1011685385"},{"seq_region_name":"7","id":"rs950512559","clinical_significance":[],"start":140447478,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140447478,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447482,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140447482,"seq_region_name":"7","id":"rs1799901087","clinical_significance":[]},{"id":"rs987424407","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140447483,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447483,"source":"dbSNP"},{"id":"rs1043505637","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140447484,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447484,"source":"dbSNP"},{"clinical_significance":[],"id":"rs748396705","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447485,"feature_type":"variation","strand":1,"end":140447485,"alleles":["G","A"]},{"clinical_significance":[],"id":"rs1799901171","seq_region_name":"7","source":"dbSNP","start":140447486,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140447486,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447487,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140447487,"id":"rs1218911424","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1286970554","seq_region_name":"7","source":"dbSNP","start":140447488,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140447488,"alleles":["C","T"],"feature_type":"variation","strand":1},{"end":140447489,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140447489,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1585452807","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799901240","clinical_significance":[],"strand":1,"feature_type":"variation","end":140447490,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447490,"source":"dbSNP"},{"alleles":["C","T"],"end":140447493,"strand":1,"feature_type":"variation","start":140447493,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1018866833","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140447495,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447495,"source":"dbSNP","seq_region_name":"7","id":"rs1165350752","clinical_significance":[]},{"id":"rs964750710","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447496,"source":"dbSNP","strand":1,"feature_type":"variation","end":140447496,"alleles":["C","T"]},{"source":"dbSNP","start":140447500,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140447500,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs903368686"},{"clinical_significance":[],"id":"rs1183565965","seq_region_name":"7","end":140447501,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140447501,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447504,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140447504,"clinical_significance":[],"seq_region_name":"7","id":"rs1799901370"},{"start":140447505,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","C","G"],"end":140447505,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1483074983","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799901408","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140447506,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447506,"source":"dbSNP"},{"start":140447507,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140447507,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2363829","clinical_significance":[]},{"start":140447508,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140447508,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1035910002","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs868461341","end":140447509,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140447509,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs915346816","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140447510,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447510,"source":"dbSNP"},{"start":140447516,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140447516,"alleles":["G","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799901499","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799901520","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447518,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140447518},{"seq_region_name":"7","id":"rs1799901549","clinical_significance":[],"start":140447524,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140447524,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447531,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140447531,"clinical_significance":[],"seq_region_name":"7","id":"rs1799901564"},{"feature_type":"variation","strand":1,"end":140447532,"alleles":["A","AA"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447532,"clinical_significance":[],"seq_region_name":"7","id":"rs530032667"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140447535,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447535,"source":"dbSNP","seq_region_name":"7","id":"rs1799901621","clinical_significance":[]},{"seq_region_name":"7","id":"rs1201500665","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140447537,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447537,"source":"dbSNP"},{"source":"dbSNP","start":140447538,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140447538,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799901676"},{"start":140447540,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140447540,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799901690","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799901709","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447542,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140447542},{"start":140447545,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140447545,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs1292543274","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447546,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140447546,"seq_region_name":"7","id":"rs1228960597","clinical_significance":[]},{"start":140447549,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","C"],"end":140447549,"strand":1,"feature_type":"variation","id":"rs1799901754","seq_region_name":"7","clinical_significance":[]},{"end":140447553,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140447553,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799901772","clinical_significance":[]},{"seq_region_name":"7","id":"rs1375493249","clinical_significance":[],"strand":1,"feature_type":"variation","end":140447555,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447555,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1799901813","seq_region_name":"7","end":140447556,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140447556,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs946762915","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447559,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140447559},{"seq_region_name":"7","id":"rs1441639478","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447561,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140447561},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447562,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140447562,"seq_region_name":"7","id":"rs2363828","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140447570,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447570,"source":"dbSNP","seq_region_name":"7","id":"rs1477889376","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs924133498","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447573,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140447573},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447573,"source":"dbSNP","strand":1,"feature_type":"variation","end":140447575,"alleles":["CCC","CC"],"seq_region_name":"7","id":"rs1799901969","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140447575,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447575,"source":"dbSNP","seq_region_name":"7","id":"rs1013117571","clinical_significance":[]},{"clinical_significance":[],"id":"rs939517182","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140447576,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447576},{"clinical_significance":[],"seq_region_name":"7","id":"rs1160426903","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447576,"feature_type":"variation","strand":1,"end":140447581,"alleles":["GGCTAA","GGCTAAGGCTAA"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799902042","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447578,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140447578},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447581,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140447581,"id":"rs1799902070","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs569799506","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140447587,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447587},{"clinical_significance":[],"seq_region_name":"7","id":"rs1469189502","alleles":["A","G"],"end":140447589,"feature_type":"variation","strand":1,"source":"dbSNP","start":140447589,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs868014061","end":140447590,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140447590,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799902161","feature_type":"variation","strand":1,"alleles":["G","C","T"],"end":140447592,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447592},{"source":"dbSNP","start":140447593,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140447596,"alleles":["TTTT","TTT"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs778737435"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563082371","end":140447598,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140447598,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1466936021","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447601,"feature_type":"variation","strand":1,"end":140447601,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1272276410","feature_type":"variation","strand":1,"end":140447604,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447604},{"source":"dbSNP","start":140447606,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140447606,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799902279","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130215776","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447609,"feature_type":"variation","strand":1,"end":140447609,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799902291","source":"dbSNP","start":140447612,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140447612,"alleles":["T","C"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140447613,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447613,"clinical_significance":[],"seq_region_name":"7","id":"rs948433482"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799902339","source":"dbSNP","start":140447614,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140447614,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799902362","alleles":["-","TA"],"end":140447615,"feature_type":"variation","strand":1,"source":"dbSNP","start":140447616,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1799902380","clinical_significance":[],"start":140447616,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140447616,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140447617,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140447617,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799902392"},{"clinical_significance":[],"id":"rs1318640732","seq_region_name":"7","source":"dbSNP","start":140447619,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140447619,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1044425766","alleles":["T","C"],"end":140447620,"feature_type":"variation","strand":1,"source":"dbSNP","start":140447620,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1223223770","source":"dbSNP","start":140447628,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140447628,"alleles":["G","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1368425763","clinical_significance":[],"start":140447630,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140447630,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1305852646","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447632,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140447632},{"seq_region_name":"7","id":"rs1438946069","clinical_significance":[],"alleles":["TCTC","TC"],"end":140447636,"strand":1,"feature_type":"variation","start":140447633,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs952366064","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447635,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140447635},{"source":"dbSNP","start":140447640,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140447640,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs77632899"},{"alleles":["T","C"],"end":140447643,"feature_type":"variation","strand":1,"source":"dbSNP","start":140447643,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1015738166","seq_region_name":"7"},{"seq_region_name":"7","id":"rs961240161","clinical_significance":[],"start":140447651,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140447651,"alleles":["A","G","T"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140447652,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140447655,"alleles":["GGTG","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1343883800"},{"clinical_significance":[],"id":"rs150486018","seq_region_name":"7","alleles":["G","A","T"],"end":140447653,"feature_type":"variation","strand":1,"source":"dbSNP","start":140447653,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"id":"rs1425296377","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447664,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140447664},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447672,"source":"dbSNP","strand":1,"feature_type":"variation","end":140447672,"alleles":["C","T"],"seq_region_name":"7","id":"rs1799902688","clinical_significance":[]},{"alleles":["T","G"],"end":140447673,"strand":1,"feature_type":"variation","start":140447673,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1194996406","clinical_significance":[]},{"seq_region_name":"7","id":"rs749349176","clinical_significance":[],"start":140447674,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140447674,"alleles":["C","G","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs886308671","clinical_significance":[],"strand":1,"feature_type":"variation","end":140447677,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447677,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1379319506","source":"dbSNP","start":140447678,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140447684,"alleles":["AAGTGCT","-"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1799902797","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447681,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140447681},{"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140447687,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447687,"clinical_significance":[],"id":"rs1188962534","seq_region_name":"7"},{"id":"rs1799902845","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140447692,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447692,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799902856","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447696,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140447696},{"seq_region_name":"7","id":"rs1486727437","clinical_significance":[],"start":140447697,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140447697,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447698,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140447698,"id":"rs922423356","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1215022962","seq_region_name":"7","source":"dbSNP","start":140447701,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140447701,"alleles":["G","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs924872390","clinical_significance":[],"strand":1,"feature_type":"variation","end":140447706,"alleles":["T","A","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447706,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs11971692","source":"dbSNP","start":140447708,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140447708,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447709,"source":"dbSNP","strand":1,"feature_type":"variation","end":140447709,"alleles":["G","A"],"id":"rs565746264","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140447711,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140447711,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799903027"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447712,"source":"dbSNP","strand":1,"feature_type":"variation","end":140447712,"alleles":["C","G"],"seq_region_name":"7","id":"rs1298618357","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1357121696","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140447713,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447713},{"seq_region_name":"7","id":"rs1384223086","clinical_significance":[],"strand":1,"feature_type":"variation","end":140447715,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447715,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1360335839","clinical_significance":[],"end":140447717,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140447717,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs191216338","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140447720,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447720,"source":"dbSNP"},{"start":140447721,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140447721,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs543264648","clinical_significance":[]},{"seq_region_name":"7","id":"rs113157060","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447723,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140447723},{"seq_region_name":"7","id":"rs528667491","clinical_significance":[],"start":140447725,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140447725,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1199603367","clinical_significance":[],"end":140447734,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140447734,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1799903267","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447737,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140447737},{"clinical_significance":[],"seq_region_name":"7","id":"rs934753907","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140447738,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447738},{"strand":1,"feature_type":"variation","end":140447743,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447743,"source":"dbSNP","id":"rs760665815","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799903322","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447748,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140447748},{"end":140447751,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140447751,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1432399373","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799903360","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447752,"feature_type":"variation","strand":1,"end":140447752,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1394030886","clinical_significance":[],"start":140447753,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140447753,"alleles":["T","C","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs924018906","clinical_significance":[],"end":140447754,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","start":140447754,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"source":"dbSNP","start":140447755,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140447755,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1437394802"},{"source":"dbSNP","start":140447758,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["GGG","GG"],"end":140447760,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs771661695"},{"clinical_significance":[],"seq_region_name":"7","id":"rs960866711","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447763,"feature_type":"variation","strand":1,"end":140447763,"alleles":["A","C"]},{"source":"dbSNP","start":140447765,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140447765,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799903482"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140447769,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447769,"source":"dbSNP","seq_region_name":"7","id":"rs2130215997","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140447771,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447771,"source":"dbSNP","seq_region_name":"7","id":"rs1177492368","clinical_significance":[]},{"id":"rs1483530539","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447775,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140447775},{"start":140447784,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140447784,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1259617152","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140447785,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447785,"source":"dbSNP","id":"rs796685912","seq_region_name":"7","clinical_significance":[]},{"id":"rs1799903579","seq_region_name":"7","clinical_significance":[],"end":140447786,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140447786,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"id":"rs1799903606","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447789,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140447789},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799903627","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447790,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140447790},{"seq_region_name":"7","id":"rs1208739178","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447793,"source":"dbSNP","strand":1,"feature_type":"variation","end":140447798,"alleles":["AAAAAA","AAAA","AAAAAAA"]},{"feature_type":"variation","strand":1,"end":140447795,"alleles":["A","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447795,"clinical_significance":[],"seq_region_name":"7","id":"rs1275565551"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447801,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140447801,"seq_region_name":"7","id":"rs1799903697","clinical_significance":[]},{"end":140447805,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140447805,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1229921910","clinical_significance":[]},{"clinical_significance":[],"id":"rs2130216034","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447812,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140447812},{"clinical_significance":[],"id":"rs547232433","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447814,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140447814},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799903753","source":"dbSNP","start":140447821,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140447821,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1306020038","clinical_significance":[],"end":140447825,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140447825,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"start":140447826,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["AA","-"],"end":140447827,"strand":1,"feature_type":"variation","id":"rs1799903802","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1295274711","source":"dbSNP","start":140447828,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140447828,"alleles":["G","A","T"],"feature_type":"variation","strand":1},{"id":"rs1357912464","seq_region_name":"7","clinical_significance":[],"end":140447831,"alleles":["T","A","G"],"strand":1,"feature_type":"variation","start":140447831,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447832,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140447832,"seq_region_name":"7","id":"rs992264464","clinical_significance":[]},{"end":140447834,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140447834,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs768437150","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799903917","source":"dbSNP","start":140447837,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140447837,"feature_type":"variation","strand":1},{"end":140447838,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140447838,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1013148668","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs916853316","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140447841,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447841,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447843,"source":"dbSNP","strand":1,"feature_type":"variation","end":140447843,"alleles":["C","T"],"seq_region_name":"7","id":"rs948336078","clinical_significance":[]},{"end":140447846,"alleles":["ATA","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140447844,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1563082419"},{"alleles":["T","C"],"end":140447845,"strand":1,"feature_type":"variation","start":140447845,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs181612477","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447850,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140447850,"seq_region_name":"7","id":"rs1038601191","clinical_significance":[]},{"clinical_significance":[],"id":"rs2130216092","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140447855,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447855},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799904052","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140447856,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447856},{"seq_region_name":"7","id":"rs1419874040","clinical_significance":[],"start":140447857,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140447857,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140447858,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447858,"source":"dbSNP","id":"rs1185745784","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs186964048","clinical_significance":[],"start":140447859,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140447859,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1197676197","clinical_significance":[],"end":140447860,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140447860,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1479771536","source":"dbSNP","start":140447864,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140447864,"alleles":["G","-"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140447866,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140447866,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799904164"},{"seq_region_name":"7","id":"rs1465955780","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["GG","G"],"end":140447868,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447867,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799904202","source":"dbSNP","start":140447871,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140447871,"alleles":["G","A"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140447872,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447872,"source":"dbSNP","seq_region_name":"7","id":"rs920295377","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447875,"source":"dbSNP","strand":1,"feature_type":"variation","end":140447875,"alleles":["G","A"],"id":"rs1585453009","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1337423315","clinical_significance":[],"end":140447876,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140447876,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs888139210","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140447877,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447877},{"start":140447879,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140447879,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799904290","clinical_significance":[]},{"start":140447880,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["CAACAA","CAA"],"end":140447885,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1047521414","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140447881,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447881,"source":"dbSNP","seq_region_name":"7","id":"rs1351699759","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447896,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GGAG","G"],"end":140447899,"seq_region_name":"7","id":"rs886151657","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["AGAAGAA","AGAA"],"end":140447904,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447898,"clinical_significance":[],"seq_region_name":"7","id":"rs144088791"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447902,"source":"dbSNP","strand":1,"feature_type":"variation","end":140447902,"alleles":["G","C"],"seq_region_name":"7","id":"rs1005593441","clinical_significance":[]},{"id":"rs1393784447","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140447905,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447905,"source":"dbSNP"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447912,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140447912,"clinical_significance":[],"seq_region_name":"7","id":"rs1799904446"},{"alleles":["A","C"],"end":140447917,"feature_type":"variation","strand":1,"source":"dbSNP","start":140447917,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799904460"},{"alleles":["GGGGG","GGGGGG"],"end":140447922,"strand":1,"feature_type":"variation","start":140447918,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799904482","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140447919,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447919,"clinical_significance":[],"seq_region_name":"7","id":"rs1799904511"},{"source":"dbSNP","start":140447920,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140447920,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799904542"},{"seq_region_name":"7","id":"rs1015353048","clinical_significance":[],"start":140447922,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140447922,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447925,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140447925,"clinical_significance":[],"seq_region_name":"7","id":"rs1799904579"},{"clinical_significance":[],"id":"rs1461722307","seq_region_name":"7","source":"dbSNP","start":140447925,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["ATAT","AT"],"end":140447928,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140447926,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447926,"source":"dbSNP","seq_region_name":"7","id":"rs1396446558","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140447928,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447928,"clinical_significance":[],"seq_region_name":"7","id":"rs2130216249"},{"seq_region_name":"7","id":"rs1162580488","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447930,"source":"dbSNP","strand":1,"feature_type":"variation","end":140447930,"alleles":["C","A","T"]},{"clinical_significance":[],"id":"rs1444770115","seq_region_name":"7","end":140447931,"alleles":["G","A","C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140447931,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447939,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140447939,"seq_region_name":"7","id":"rs1330900363","clinical_significance":[]},{"end":140447942,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140447942,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs551087677","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799904732","seq_region_name":"7","source":"dbSNP","start":140447943,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","A","C"],"end":140447943,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799904755","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140447945,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447945},{"seq_region_name":"7","id":"rs1799904769","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447948,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140447948},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447949,"source":"dbSNP","strand":1,"feature_type":"variation","end":140447949,"alleles":["T","C","G"],"seq_region_name":"7","id":"rs776418139","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447951,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140447951,"seq_region_name":"7","id":"rs1799904815","clinical_significance":[]},{"alleles":["G","A"],"end":140447960,"feature_type":"variation","strand":1,"source":"dbSNP","start":140447960,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799904834"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447961,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140447961,"clinical_significance":[],"seq_region_name":"7","id":"rs1417409419"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1250014205","feature_type":"variation","strand":1,"end":140447968,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447968},{"start":140447969,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140447969,"strand":1,"feature_type":"variation","id":"rs1210685025","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799904899","clinical_significance":[],"strand":1,"feature_type":"variation","end":140447970,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447970,"source":"dbSNP"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447972,"feature_type":"variation","strand":1,"end":140447972,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799904912"},{"source":"dbSNP","start":140447973,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140447973,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs569676250"},{"end":140447974,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140447974,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs976496164","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140447975,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447975,"source":"dbSNP","seq_region_name":"7","id":"rs2130216355","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799904978","clinical_significance":[],"strand":1,"feature_type":"variation","end":140447981,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447981,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140447984,"source":"dbSNP","strand":1,"feature_type":"variation","end":140447988,"alleles":["AAAAA","AAAA"],"seq_region_name":"7","id":"rs1271635503","clinical_significance":[]},{"source":"dbSNP","start":140447995,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140447995,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs11971769"},{"clinical_significance":[],"seq_region_name":"7","id":"rs996520244","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140447996,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140447996},{"id":"rs1799905131","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140448007,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448007,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1263020065","alleles":["C","A","T"],"end":140448014,"feature_type":"variation","strand":1,"source":"dbSNP","start":140448014,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs117637380","seq_region_name":"7","source":"dbSNP","start":140448015,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140448015,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1305796377","clinical_significance":[],"end":140448017,"alleles":["A","G","T"],"strand":1,"feature_type":"variation","start":140448017,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"start":140448018,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140448018,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1441150291","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140448019,"alleles":["G","-"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448019,"clinical_significance":[],"seq_region_name":"7","id":"rs1372791821"},{"alleles":["C","T"],"end":140448024,"strand":1,"feature_type":"variation","start":140448024,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1323634612","clinical_significance":[]},{"clinical_significance":[],"id":"rs1385499222","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448026,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140448026},{"clinical_significance":[],"seq_region_name":"7","id":"rs1460790534","feature_type":"variation","strand":1,"alleles":["CTCAAACTCAA","CTCAA"],"end":140448036,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448026},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799905285","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448028,"feature_type":"variation","strand":1,"end":140448028,"alleles":["C","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1160241671","end":140448029,"alleles":["A","C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140448029,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1356184409","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140448032,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448032,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448033,"source":"dbSNP","strand":1,"feature_type":"variation","end":140448033,"alleles":["T","C"],"id":"rs1799905331","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799905345","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140448037,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448037,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799905365","alleles":["T","C"],"end":140448041,"feature_type":"variation","strand":1,"source":"dbSNP","start":140448041,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"id":"rs1451661112","seq_region_name":"7","clinical_significance":[],"start":140448042,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140448042,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1799905404","seq_region_name":"7","feature_type":"variation","strand":1,"end":140448045,"alleles":["CCC","CC"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448043},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799905419","feature_type":"variation","strand":1,"end":140448044,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448044},{"id":"rs867734482","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448049,"source":"dbSNP","strand":1,"feature_type":"variation","end":140448049,"alleles":["C","T"]},{"clinical_significance":[],"id":"rs1022208302","seq_region_name":"7","source":"dbSNP","start":140448050,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140448050,"feature_type":"variation","strand":1},{"start":140448054,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","G","T"],"end":140448054,"strand":1,"feature_type":"variation","id":"rs968053446","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1260342773","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448057,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140448057},{"source":"dbSNP","start":140448061,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140448061,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs999447811"},{"end":140448065,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140448065,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs915121931","clinical_significance":[]},{"seq_region_name":"7","id":"rs1197668436","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448069,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["ATAT","AT"],"end":140448072},{"clinical_significance":[],"seq_region_name":"7","id":"rs1031046441","feature_type":"variation","strand":1,"end":140448072,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448072},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448073,"feature_type":"variation","strand":1,"end":140448073,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799905592"},{"end":140448075,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140448075,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1350633918","clinical_significance":[]},{"start":140448076,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","G"],"end":140448076,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1259610607","clinical_significance":[]},{"end":140448077,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140448077,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799905639"},{"seq_region_name":"7","id":"rs947416020","clinical_significance":[],"start":140448081,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G","T"],"end":140448081,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130216507","source":"dbSNP","start":140448084,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140448084,"feature_type":"variation","strand":1},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448085,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140448085,"clinical_significance":[],"id":"rs1349596550","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140448088,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448088,"source":"dbSNP","seq_region_name":"7","id":"rs552468011","clinical_significance":[]},{"source":"dbSNP","start":140448090,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140448090,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799905716"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799905739","source":"dbSNP","start":140448091,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140448091,"alleles":["G","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799905754","feature_type":"variation","strand":1,"alleles":["TAAGTAA","TAA"],"end":140448101,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448095},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448098,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140448098,"clinical_significance":[],"seq_region_name":"7","id":"rs1799905778"},{"seq_region_name":"7","id":"rs1300814132","clinical_significance":[],"start":140448099,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140448121,"alleles":["TAATAGAATAACAGCTGTTATTA","TA"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140448100,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140448101,"alleles":["AA","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1443697033"},{"seq_region_name":"7","id":"rs6962710","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448102,"source":"dbSNP","strand":1,"feature_type":"variation","end":140448102,"alleles":["T","A","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563082464","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448103,"feature_type":"variation","strand":1,"alleles":["A","-"],"end":140448103},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140448104,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448104,"source":"dbSNP","seq_region_name":"7","id":"rs1799905922","clinical_significance":[]},{"alleles":["A","G"],"end":140448106,"feature_type":"variation","strand":1,"source":"dbSNP","start":140448106,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs924631287"},{"alleles":["T","C"],"end":140448107,"feature_type":"variation","strand":1,"source":"dbSNP","start":140448107,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs969580964","seq_region_name":"7"},{"seq_region_name":"7","id":"rs546712635","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448107,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TAACAGCTGTTATTATTAG","-"],"end":140448125},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130216589","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140448110,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448110},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799906010","source":"dbSNP","start":140448112,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140448112,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1380435862","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448114,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TGTT","T"],"end":140448117},{"start":140448119,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140448119,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs534492244","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140448120,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448120,"clinical_significance":[],"seq_region_name":"7","id":"rs1057127807"},{"seq_region_name":"7","id":"rs895999202","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448123,"source":"dbSNP","strand":1,"feature_type":"variation","end":140448123,"alleles":["T","C","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1393439061","alleles":["TAG","-"],"end":140448125,"feature_type":"variation","strand":1,"source":"dbSNP","start":140448123,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs867141976","source":"dbSNP","start":140448125,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140448125,"feature_type":"variation","strand":1},{"alleles":["T","C"],"end":140448131,"feature_type":"variation","strand":1,"source":"dbSNP","start":140448131,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1236836833"},{"feature_type":"variation","strand":1,"alleles":["AAAAA","AAAA"],"end":140448138,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448134,"clinical_significance":[],"seq_region_name":"7","id":"rs35672617"},{"end":140448142,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140448142,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs920141818"},{"start":140448143,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140448143,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799906229","clinical_significance":[]},{"start":140448146,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140448146,"alleles":["A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799906244","clinical_significance":[]},{"id":"rs1258915387","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448146,"source":"dbSNP","strand":1,"feature_type":"variation","end":140448153,"alleles":["AAAGAAAG","AAAG"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1342813448","source":"dbSNP","start":140448149,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","-"],"end":140448149,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1799906311","seq_region_name":"7","end":140448154,"alleles":["GG","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140448153,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"id":"rs1478082170","seq_region_name":"7","clinical_significance":[],"alleles":["T","A"],"end":140448157,"strand":1,"feature_type":"variation","start":140448157,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1210895985","feature_type":"variation","strand":1,"end":140448175,"alleles":["GGCCTTTCAACGTCGCA","GGCCTTTCAACGTCGCAGGCCTTTCAACGTCGCA"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448159},{"clinical_significance":[],"seq_region_name":"7","id":"rs1486375708","alleles":["C","T"],"end":140448161,"feature_type":"variation","strand":1,"source":"dbSNP","start":140448161,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448164,"source":"dbSNP","strand":1,"feature_type":"variation","end":140448164,"alleles":["T","G"],"seq_region_name":"7","id":"rs948868490","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448165,"feature_type":"variation","strand":1,"end":140448165,"alleles":["T","C"],"clinical_significance":[],"id":"rs1044632813","seq_region_name":"7"},{"start":140448166,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","G","T"],"end":140448166,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs888664045","clinical_significance":[]},{"id":"rs1464907896","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140448169,"strand":1,"feature_type":"variation","start":140448169,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"alleles":["G","A"],"end":140448170,"feature_type":"variation","strand":1,"source":"dbSNP","start":140448170,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1271701113","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1167620242","clinical_significance":[],"strand":1,"feature_type":"variation","end":140448172,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448172,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs552775155","end":140448173,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140448173,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140448174,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140448174,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs907637672"},{"clinical_significance":[],"id":"rs2130216709","seq_region_name":"7","alleles":["A","C"],"end":140448175,"feature_type":"variation","strand":1,"source":"dbSNP","start":140448175,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"alleles":["C","G"],"end":140448177,"feature_type":"variation","strand":1,"source":"dbSNP","start":140448177,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130216715"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799906568","alleles":["A","G"],"end":140448179,"feature_type":"variation","strand":1,"source":"dbSNP","start":140448179,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"alleles":["T","C"],"end":140448186,"feature_type":"variation","strand":1,"source":"dbSNP","start":140448186,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1005796000"},{"id":"rs1799906590","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448190,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140448190},{"clinical_significance":[],"id":"rs1563082491","seq_region_name":"7","end":140448191,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140448191,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448194,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140448194,"clinical_significance":[],"id":"rs1799906627","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799906641","source":"dbSNP","start":140448197,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140448197,"alleles":["C","G"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140448198,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448198,"clinical_significance":[],"seq_region_name":"7","id":"rs1799906655"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448199,"feature_type":"variation","strand":1,"end":140448199,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs577710813"},{"start":140448199,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["AC","ACAC"],"end":140448200,"strand":1,"feature_type":"variation","id":"rs1799906696","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799906716","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448201,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["-","G"],"end":140448200},{"seq_region_name":"7","id":"rs1373739648","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448204,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140448204},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799906746","source":"dbSNP","start":140448205,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140448205,"alleles":["C","G"],"feature_type":"variation","strand":1},{"id":"rs1799906765","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140448210,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448210,"source":"dbSNP"},{"start":140448212,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140448212,"alleles":["G","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799906790","clinical_significance":[]},{"id":"rs1799906814","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448213,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140448213},{"end":140448214,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140448214,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799906827","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799906845","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448215,"source":"dbSNP","strand":1,"feature_type":"variation","end":140448215,"alleles":["C","T"]},{"strand":1,"feature_type":"variation","end":140448217,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448217,"source":"dbSNP","seq_region_name":"7","id":"rs1799906863","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448222,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140448222,"clinical_significance":[],"seq_region_name":"7","id":"rs1312391056"},{"end":140448224,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140448224,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799906908","clinical_significance":[]},{"alleles":["A","G"],"end":140448225,"strand":1,"feature_type":"variation","start":140448225,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799906930","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1015715270","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448227,"feature_type":"variation","strand":1,"end":140448227,"alleles":["C","T"]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140448228,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448228,"clinical_significance":[],"seq_region_name":"7","id":"rs896801321"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448229,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140448229,"seq_region_name":"7","id":"rs1166517354","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448230,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140448230,"clinical_significance":[],"seq_region_name":"7","id":"rs183503880"},{"start":140448231,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140448231,"alleles":["A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs74317189","clinical_significance":[]},{"start":140448242,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140448242,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799907060","clinical_significance":[]},{"end":140448243,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140448243,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs534967430","clinical_significance":[]},{"start":140448246,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140448246,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs1799907104","seq_region_name":"7","clinical_significance":[]},{"id":"rs1799907123","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140448248,"strand":1,"feature_type":"variation","start":140448248,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799907136","source":"dbSNP","start":140448252,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140448252,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563082504","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448253,"feature_type":"variation","strand":1,"alleles":["A","ACA"],"end":140448253},{"seq_region_name":"7","id":"rs1401197200","clinical_significance":[],"start":140448257,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140448257,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140448258,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448258,"clinical_significance":[],"seq_region_name":"7","id":"rs1280612976"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140448260,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448260,"source":"dbSNP","seq_region_name":"7","id":"rs1799907216","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140448261,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448261,"clinical_significance":[],"id":"rs2130216871","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799907235","clinical_significance":[],"start":140448263,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","A"],"end":140448263,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs2130216877","clinical_significance":[],"alleles":["C","T"],"end":140448264,"strand":1,"feature_type":"variation","start":140448264,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448265,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140448265,"id":"rs1799907252","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs575546623","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448267,"source":"dbSNP","strand":1,"feature_type":"variation","end":140448267,"alleles":["T","C"]},{"feature_type":"variation","strand":1,"end":140448269,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448269,"clinical_significance":[],"id":"rs1799907289","seq_region_name":"7"},{"seq_region_name":"7","id":"rs553621675","clinical_significance":[],"start":140448270,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140448270,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"id":"rs1799907327","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448273,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140448273},{"source":"dbSNP","start":140448275,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140448275,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1316513571"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799907377","end":140448279,"alleles":["TACA","TACATACA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140448276,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1438041535","clinical_significance":[],"start":140448278,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140448278,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448280,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140448280,"id":"rs542677232","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799907437","clinical_significance":[],"alleles":["T","A"],"end":140448282,"strand":1,"feature_type":"variation","start":140448282,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1799907455","clinical_significance":[],"strand":1,"feature_type":"variation","end":140448284,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448284,"source":"dbSNP"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448284,"feature_type":"variation","strand":1,"end":140448286,"alleles":["CTT","-"],"clinical_significance":[],"seq_region_name":"7","id":"rs996013969"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448288,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140448288,"clinical_significance":[],"seq_region_name":"7","id":"rs2130216919"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448291,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140448291,"seq_region_name":"7","id":"rs1317089972","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","-"],"end":140448303,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448303,"clinical_significance":[],"id":"rs1346600025","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140448304,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448304,"clinical_significance":[],"seq_region_name":"7","id":"rs1293785258"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1235023592","alleles":["C","T"],"end":140448307,"feature_type":"variation","strand":1,"source":"dbSNP","start":140448307,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140448312,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140448312,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs749913267"},{"seq_region_name":"7","id":"rs1799907599","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448313,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140448313},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799907613","end":140448314,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140448314,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1799907638","seq_region_name":"7","source":"dbSNP","start":140448315,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140448315,"alleles":["T","G"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140448319,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140448319,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1029389729","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140448320,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448320,"source":"dbSNP","seq_region_name":"7","id":"rs146950950","clinical_significance":[]},{"alleles":["A","G","T"],"end":140448326,"feature_type":"variation","strand":1,"source":"dbSNP","start":140448326,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs573615335"},{"start":140448327,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140448327,"alleles":["G","GG"],"strand":1,"feature_type":"variation","id":"rs1488317390","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140448330,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448330,"clinical_significance":[],"seq_region_name":"7","id":"rs2130216980"},{"seq_region_name":"7","id":"rs1195848006","clinical_significance":[],"start":140448332,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["AAA","AA"],"end":140448334,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs903740213","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448333,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140448333},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140448335,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448335,"source":"dbSNP","seq_region_name":"7","id":"rs766032329","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140448344,"alleles":["AAA","AA"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448342,"source":"dbSNP","seq_region_name":"7","id":"rs1799907818","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799907843","clinical_significance":[],"end":140448348,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140448348,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1409702935","end":140448349,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140448349,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1585453251","clinical_significance":[],"start":140448349,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140448356,"alleles":["AAATCAAA","AAA"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs752096613","source":"dbSNP","start":140448350,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140448350,"alleles":["A","C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1022119983","clinical_significance":[],"end":140448353,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140448353,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"strand":1,"feature_type":"variation","end":140448365,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448365,"source":"dbSNP","seq_region_name":"7","id":"rs374139336","clinical_significance":[]},{"seq_region_name":"7","id":"rs565526292","clinical_significance":[],"start":140448366,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","G","T"],"end":140448366,"strand":1,"feature_type":"variation"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448367,"feature_type":"variation","strand":1,"end":140448367,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1378461541"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448368,"source":"dbSNP","strand":1,"feature_type":"variation","end":140448368,"alleles":["T","C"],"id":"rs1467731815","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs978014428","alleles":["A","G"],"end":140448371,"feature_type":"variation","strand":1,"source":"dbSNP","start":140448371,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1457071216","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["TTT","TT"],"end":140448374,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448372,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799908046","source":"dbSNP","start":140448379,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140448379,"alleles":["G","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1171015409","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448380,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140448380},{"seq_region_name":"7","id":"rs1799908088","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448382,"source":"dbSNP","strand":1,"feature_type":"variation","end":140448382,"alleles":["G","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799908102","source":"dbSNP","start":140448389,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140448389,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1799908111","clinical_significance":[],"strand":1,"feature_type":"variation","end":140448390,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448390,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1023712101","alleles":["C","G","T"],"end":140448391,"feature_type":"variation","strand":1,"source":"dbSNP","start":140448391,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448392,"source":"dbSNP","strand":1,"feature_type":"variation","end":140448392,"alleles":["T","C"],"seq_region_name":"7","id":"rs924633419","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799908155","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448394,"source":"dbSNP","strand":1,"feature_type":"variation","end":140448394,"alleles":["A","T"]},{"feature_type":"variation","strand":1,"end":140448396,"alleles":["T","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448396,"clinical_significance":[],"seq_region_name":"7","id":"rs2130217090"},{"clinical_significance":[],"seq_region_name":"7","id":"rs533050318","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140448403,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448403},{"alleles":["G","A"],"end":140448404,"feature_type":"variation","strand":1,"source":"dbSNP","start":140448404,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1420377925"},{"feature_type":"variation","strand":1,"end":140448409,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448409,"clinical_significance":[],"id":"rs1300652952","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799908239","clinical_significance":[],"start":140448414,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140448414,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140448421,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140448421,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799908261","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1027259940","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448424,"source":"dbSNP","strand":1,"feature_type":"variation","end":140448424,"alleles":["A","T"]},{"start":140448425,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140448425,"alleles":["T","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1563082536","clinical_significance":[]},{"id":"rs951579122","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["TTTTTTTTTTT","TTTTTT","TTTTTTTTTT","TTTTTTTTTTTT"],"end":140448435,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448425,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799908373","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448427,"source":"dbSNP","strand":1,"feature_type":"variation","end":140448427,"alleles":["T","A"]},{"seq_region_name":"7","id":"rs1799908397","clinical_significance":[],"end":140448429,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140448429,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1799908413","clinical_significance":[],"end":140448430,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140448430,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799908423","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448431,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140448431},{"id":"rs1585453305","seq_region_name":"7","clinical_significance":[],"start":140448432,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140448432,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1585453307","clinical_significance":[],"start":140448438,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140448438,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1372064503","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140448440,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448440,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140448441,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448441,"clinical_significance":[],"seq_region_name":"7","id":"rs1328339861"},{"seq_region_name":"7","id":"rs1460210048","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448447,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","G"],"end":140448447},{"source":"dbSNP","start":140448448,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140448448,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1394313551"},{"clinical_significance":[],"seq_region_name":"7","id":"rs187984934","source":"dbSNP","start":140448449,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140448449,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs563244572","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140448450,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448450},{"seq_region_name":"7","id":"rs1799908571","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140448454,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448454,"source":"dbSNP"},{"start":140448455,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140448455,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs189717462","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799908620","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140448457,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448457,"source":"dbSNP"},{"start":140448459,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140448459,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs535973807","clinical_significance":[]},{"id":"rs1585453327","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140448468,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448468,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1438676749","end":140448471,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140448471,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1253317234","alleles":["A","G"],"end":140448472,"feature_type":"variation","strand":1,"source":"dbSNP","start":140448472,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"end":140448473,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140448473,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799908727","seq_region_name":"7"},{"source":"dbSNP","start":140448474,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140448474,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs910049277","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799908761","clinical_significance":[],"start":140448476,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140448476,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"start":140448477,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","G"],"end":140448477,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799908782","clinical_significance":[]},{"id":"rs1799908795","seq_region_name":"7","clinical_significance":[],"start":140448478,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140448478,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140448479,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C","G"],"end":140448479,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1230664254"},{"strand":1,"feature_type":"variation","end":140448481,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448481,"source":"dbSNP","seq_region_name":"7","id":"rs921664906","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448483,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140448483,"clinical_significance":[],"id":"rs941632513","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140448484,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448484,"clinical_significance":[],"id":"rs2130217230","seq_region_name":"7"},{"seq_region_name":"7","id":"rs567199620","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448486,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","G","T"],"end":140448486},{"clinical_significance":[],"id":"rs755606532","seq_region_name":"7","source":"dbSNP","start":140448487,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140448487,"alleles":["G","A"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140448491,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448491,"source":"dbSNP","id":"rs997812607","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140448492,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140448492,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs534645022"},{"strand":1,"feature_type":"variation","end":140448493,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448493,"source":"dbSNP","seq_region_name":"7","id":"rs1799908974","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140448495,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448495,"source":"dbSNP","seq_region_name":"7","id":"rs1239588667","clinical_significance":[]},{"source":"dbSNP","start":140448496,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140448496,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs889573264"},{"id":"rs536234292","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140448500,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448500,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1439095894","clinical_significance":[],"alleles":["C","T"],"end":140448502,"strand":1,"feature_type":"variation","start":140448502,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"id":"rs546377825","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140448503,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448503},{"end":140448505,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140448505,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1283807504","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448509,"feature_type":"variation","strand":1,"end":140448513,"alleles":["AGGAG","AG"],"clinical_significance":[],"id":"rs1799909108","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799909127","feature_type":"variation","strand":1,"alleles":["G","C","T"],"end":140448513,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448513},{"id":"rs1799909144","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140448518,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448518,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1006641805","source":"dbSNP","start":140448520,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140448520,"alleles":["A","G","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1487899612","end":140448521,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140448521,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs781027464","clinical_significance":[],"end":140448524,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140448524,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"strand":1,"feature_type":"variation","end":140448525,"alleles":["C","A","G","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448525,"source":"dbSNP","id":"rs1344003532","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448526,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140448526,"seq_region_name":"7","id":"rs1315603909","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1022570444","source":"dbSNP","start":140448531,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140448531,"feature_type":"variation","strand":1},{"end":140448532,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140448532,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs935274799","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140448534,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448534,"clinical_significance":[],"id":"rs1799909297","seq_region_name":"7"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448536,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140448536,"clinical_significance":[],"seq_region_name":"7","id":"rs143538066"},{"clinical_significance":[],"seq_region_name":"7","id":"rs999860567","source":"dbSNP","start":140448537,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140448537,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs2130217348","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448538,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140448538},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448539,"source":"dbSNP","strand":1,"feature_type":"variation","end":140448539,"alleles":["T","A"],"seq_region_name":"7","id":"rs1799909340","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799909369","clinical_significance":[],"alleles":["A","G"],"end":140448543,"strand":1,"feature_type":"variation","start":140448543,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs538458384","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140448545,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448545},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448546,"feature_type":"variation","strand":1,"alleles":["C","A","G","T"],"end":140448546,"clinical_significance":[],"seq_region_name":"7","id":"rs1030893004"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448547,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140448547,"seq_region_name":"7","id":"rs956045572","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799909466","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448554,"feature_type":"variation","strand":1,"end":140448554,"alleles":["A","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1424172190","feature_type":"variation","strand":1,"end":140448555,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448555},{"id":"rs1585453389","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448557,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140448557},{"id":"rs896527350","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140448568,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448568,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs992757390","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448569,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140448569},{"id":"rs1240288775","seq_region_name":"7","clinical_significance":[],"end":140448576,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140448576,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1197108383","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448579,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140448579},{"seq_region_name":"7","id":"rs1799909595","clinical_significance":[],"start":140448579,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["GTGGTG","GTG"],"end":140448584,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799909612","alleles":["T","C"],"end":140448586,"feature_type":"variation","strand":1,"source":"dbSNP","start":140448586,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs557399107","clinical_significance":[],"start":140448587,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140448587,"strand":1,"feature_type":"variation"},{"alleles":["C","T"],"end":140448590,"feature_type":"variation","strand":1,"source":"dbSNP","start":140448590,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs750120181","seq_region_name":"7"},{"start":140448591,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A","T"],"end":140448591,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs980193748","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448596,"feature_type":"variation","strand":1,"end":140448596,"alleles":["T","G"],"clinical_significance":[],"id":"rs1799909718","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448597,"source":"dbSNP","strand":1,"feature_type":"variation","end":140448597,"alleles":["A","C"],"seq_region_name":"7","id":"rs1799909737","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799909753","clinical_significance":[],"start":140448599,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140448599,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs910071199","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448602,"feature_type":"variation","strand":1,"end":140448602,"alleles":["C","T"]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448603,"feature_type":"variation","strand":1,"end":140448603,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs753014913"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799909824","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448604,"feature_type":"variation","strand":1,"end":140448604,"alleles":["G","A"]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448608,"source":"dbSNP","strand":1,"feature_type":"variation","end":140448608,"alleles":["C","T"],"seq_region_name":"7","id":"rs1453611768","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799909868","clinical_significance":[],"strand":1,"feature_type":"variation","end":140448610,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448610,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799909937","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448611,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140448611},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448613,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140448613,"clinical_significance":[],"seq_region_name":"7","id":"rs1037708940"},{"seq_region_name":"7","id":"rs996090609","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140448615,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448615,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140448616,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448616,"source":"dbSNP","seq_region_name":"7","id":"rs1585453426","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448618,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140448618,"clinical_significance":[],"seq_region_name":"7","id":"rs1799910392"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140448621,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448621,"clinical_significance":[],"id":"rs1216754594","seq_region_name":"7"},{"source":"dbSNP","start":140448623,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140448623,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1360413820","seq_region_name":"7"},{"start":140448626,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A","C"],"end":140448626,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs377510596","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140448629,"alleles":["A","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448629,"clinical_significance":[],"id":"rs1298140496","seq_region_name":"7"},{"start":140448630,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140448630,"strand":1,"feature_type":"variation","id":"rs1799910468","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1398799511","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140448632,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448632},{"alleles":["G","A","T"],"end":140448633,"strand":1,"feature_type":"variation","start":140448633,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs756310328","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1027184579","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448634,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140448634},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448635,"feature_type":"variation","strand":1,"end":140448635,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1314218793"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140448637,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448637,"source":"dbSNP","seq_region_name":"7","id":"rs1464212794","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140448638,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448638,"source":"dbSNP","seq_region_name":"7","id":"rs1799910581","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140448639,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448639,"source":"dbSNP","seq_region_name":"7","id":"rs1585453444","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1385446360","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448640,"feature_type":"variation","strand":1,"end":140448640,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1302259170","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448642,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140448642},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140448643,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448643,"clinical_significance":[],"seq_region_name":"7","id":"rs934222412"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1417240171","source":"dbSNP","start":140448646,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140448646,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448649,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140448649,"seq_region_name":"7","id":"rs1192892732","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448650,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140448650,"seq_region_name":"7","id":"rs755673844","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799910642","end":140448651,"alleles":["GG","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140448650,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs983070536","alleles":["A","T"],"end":140448652,"feature_type":"variation","strand":1,"source":"dbSNP","start":140448652,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1019868410","source":"dbSNP","start":140448653,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140448653,"alleles":["G","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1799910839","clinical_significance":[],"start":140448654,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140448654,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140448663,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140448663,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799910901","seq_region_name":"7"},{"start":140448672,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140448672,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs779911021","clinical_significance":[]},{"source":"dbSNP","start":140448673,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140448673,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1006671467"},{"seq_region_name":"7","id":"rs1799910985","clinical_significance":[],"end":140448677,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140448677,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1799911005","clinical_significance":[],"alleles":["C","T"],"end":140448679,"strand":1,"feature_type":"variation","start":140448679,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140448685,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448685,"source":"dbSNP","id":"rs1222269324","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs145919206","source":"dbSNP","start":140448690,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","A","G"],"end":140448690,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799911080","alleles":["G","C"],"end":140448693,"feature_type":"variation","strand":1,"source":"dbSNP","start":140448693,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs6951446","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448695,"feature_type":"variation","strand":1,"end":140448695,"alleles":["C","A","T"]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140448696,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448696,"source":"dbSNP","seq_region_name":"7","id":"rs555032374","clinical_significance":[]},{"clinical_significance":[],"id":"rs1294581474","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448701,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140448701},{"end":140448707,"alleles":["GAGTGAG","GAG"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140448701,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799911240","seq_region_name":"7"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448702,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140448702,"clinical_significance":[],"id":"rs1799911254","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1393858139","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448704,"feature_type":"variation","strand":1,"end":140448704,"alleles":["T","A"]},{"id":"rs1377917482","seq_region_name":"7","clinical_significance":[],"start":140448705,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140448705,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"start":140448706,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140448706,"alleles":["A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs979134609","clinical_significance":[]},{"alleles":["G","C"],"end":140448707,"strand":1,"feature_type":"variation","start":140448707,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1208954841","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs182618873","alleles":["C","T"],"end":140448709,"feature_type":"variation","strand":1,"source":"dbSNP","start":140448709,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1169756044","clinical_significance":[],"start":140448710,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140448710,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1458352175","end":140448712,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140448712,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"end":140448713,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140448713,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs563148983"},{"feature_type":"variation","strand":1,"end":140448714,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448714,"clinical_significance":[],"id":"rs1185423672","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799911580","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448717,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140448717},{"start":140448718,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140448718,"alleles":["A","T"],"strand":1,"feature_type":"variation","id":"rs896443765","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs57763594","feature_type":"variation","strand":1,"end":140448748,"alleles":["AAATAAATAAATAAATAAATAAATAAATAA","AAATAAATAAATAA","AAATAAATAAATAAATAA","AAATAAATAAATAAATAAATAA","AAATAAATAAATAAATAAATAAATAA","AAATAAATAAATAAATAAATAAATAAATAAATAA","AAATAAATAAATAAATAAATAAATAAATAAATAAATAA","AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAA","AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAA","AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAA","AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAA","AAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAA"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448719},{"feature_type":"variation","strand":1,"alleles":["AATAAAT","AATAAATCAATAAAT"],"end":140448726,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448720,"clinical_significance":[],"id":"rs1799911932","seq_region_name":"7"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448722,"feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140448722,"clinical_significance":[],"seq_region_name":"7","id":"rs1013455117"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140448724,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448724,"source":"dbSNP","id":"rs1024284200","seq_region_name":"7","clinical_significance":[]},{"end":140448728,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140448728,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs970019964","clinical_significance":[]},{"seq_region_name":"7","id":"rs1374265785","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448729,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["ATA","ATACATA"],"end":140448731},{"seq_region_name":"7","id":"rs905178656","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140448730,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448730,"source":"dbSNP"},{"id":"rs1585453539","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140448731,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448731,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140448733,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448733,"source":"dbSNP","seq_region_name":"7","id":"rs1180606668","clinical_significance":[]},{"id":"rs1396518585","seq_region_name":"7","clinical_significance":[],"alleles":["TAA","TAAGTAA"],"end":140448736,"strand":1,"feature_type":"variation","start":140448734,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799912140","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448737,"feature_type":"variation","strand":1,"end":140448739,"alleles":["ATA","ATACATA"]},{"strand":1,"feature_type":"variation","end":140448738,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448738,"source":"dbSNP","seq_region_name":"7","id":"rs1799912164","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799912182","clinical_significance":[],"strand":1,"feature_type":"variation","end":140448740,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448740,"source":"dbSNP"},{"start":140448741,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140448741,"alleles":["A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1457438911","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448741,"source":"dbSNP","strand":1,"feature_type":"variation","end":140448748,"alleles":["ATAAATAA","ATAAATAAATACATAAATAA"],"id":"rs1161418654","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140448743,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140448743,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1364428497","seq_region_name":"7"},{"start":140448744,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140448744,"alleles":["A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799912264","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799912290","seq_region_name":"7","feature_type":"variation","strand":1,"end":140448745,"alleles":["A","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448745},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448747,"source":"dbSNP","strand":1,"feature_type":"variation","end":140448747,"alleles":["A","G"],"id":"rs1418543752","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1378595179","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448747,"source":"dbSNP","strand":1,"feature_type":"variation","end":140448748,"alleles":["AA","AAA"]},{"alleles":["T","A"],"end":140448749,"strand":1,"feature_type":"variation","start":140448749,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1161441699","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799912369","feature_type":"variation","strand":1,"end":140448758,"alleles":["C","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448758},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140448759,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448759,"clinical_significance":[],"seq_region_name":"7","id":"rs1166186921"},{"clinical_significance":[],"id":"rs1799912422","seq_region_name":"7","feature_type":"variation","strand":1,"end":140448763,"alleles":["C","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448763},{"start":140448769,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140448769,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs995626760","clinical_significance":[]},{"source":"dbSNP","start":140448772,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G","T"],"end":140448772,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1194586680","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448773,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140448773,"seq_region_name":"7","id":"rs1799912497","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140448774,"alleles":["G","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448774,"clinical_significance":[],"seq_region_name":"7","id":"rs1799912515"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448780,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140448780,"clinical_significance":[],"seq_region_name":"7","id":"rs1799912534"},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140448782,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448782,"source":"dbSNP","seq_region_name":"7","id":"rs1799912552","clinical_significance":[]},{"alleles":["C","T"],"end":140448787,"strand":1,"feature_type":"variation","start":140448787,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1470124268","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448790,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140448790,"clinical_significance":[],"id":"rs1456721759","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1209732764","clinical_significance":[],"alleles":["T","C"],"end":140448791,"strand":1,"feature_type":"variation","start":140448791,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140448794,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448794,"clinical_significance":[],"id":"rs1352098104","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1260785098","alleles":["G","A"],"end":140448797,"feature_type":"variation","strand":1,"source":"dbSNP","start":140448797,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799912673","end":140448802,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140448802,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799912686","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140448804,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448804},{"source":"dbSNP","start":140448804,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140448807,"alleles":["GGGG","GGG"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1325606075"},{"feature_type":"variation","strand":1,"end":140448808,"alleles":["C","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448808,"clinical_significance":[],"id":"rs540969372","seq_region_name":"7"},{"alleles":["AGAAGAA","AGAA"],"end":140448815,"strand":1,"feature_type":"variation","start":140448809,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1308092351","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140448810,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448810,"source":"dbSNP","seq_region_name":"7","id":"rs1448598388","clinical_significance":[]},{"end":140448811,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140448811,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1328836670","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","A","G"],"end":140448816,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448816,"clinical_significance":[],"seq_region_name":"7","id":"rs887308205"},{"start":140448820,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["CT","-"],"end":140448821,"strand":1,"feature_type":"variation","id":"rs1799912829","seq_region_name":"7","clinical_significance":[]},{"id":"rs559304511","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140448821,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448821,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs963211050","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448822,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140448822},{"source":"dbSNP","start":140448823,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140448823,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1385655851"},{"source":"dbSNP","start":140448824,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140448824,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1314786637","seq_region_name":"7"},{"seq_region_name":"7","id":"rs972960251","clinical_significance":[],"start":140448825,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140448825,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799912953","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448826,"feature_type":"variation","strand":1,"end":140448826,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1782883911","clinical_significance":[],"start":140448827,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140448827,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140448828,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448828,"clinical_significance":[],"seq_region_name":"7","id":"rs1379859428"},{"id":"rs565564517","seq_region_name":"7","clinical_significance":[],"alleles":["GGGGG","GGGGGG"],"end":140448833,"strand":1,"feature_type":"variation","start":140448829,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"id":"rs1799913021","seq_region_name":"7","source":"dbSNP","start":140448830,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140448830,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs188084218","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448834,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140448834},{"seq_region_name":"7","id":"rs1799913068","clinical_significance":[],"strand":1,"feature_type":"variation","end":140448846,"alleles":["GCTACAGC","GC"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448839,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1455776244","feature_type":"variation","strand":1,"end":140448843,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448843},{"seq_region_name":"7","id":"rs1258409687","clinical_significance":[],"strand":1,"feature_type":"variation","end":140448844,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448844,"source":"dbSNP"},{"start":140448852,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","T"],"end":140448852,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs192803646","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448854,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140448854,"seq_region_name":"7","id":"rs1563082647","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1198668995","end":140448855,"alleles":["AA","AAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140448854,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"id":"rs563363827","seq_region_name":"7","clinical_significance":[],"start":140448863,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140448863,"alleles":["A","C","T"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140448868,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140448868,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs997603504"},{"alleles":["T","C"],"end":140448870,"feature_type":"variation","strand":1,"source":"dbSNP","start":140448870,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799913244"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1319705134","source":"dbSNP","start":140448871,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140448871,"feature_type":"variation","strand":1},{"id":"rs1799913278","seq_region_name":"7","clinical_significance":[],"start":140448875,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","G"],"end":140448875,"strand":1,"feature_type":"variation"},{"id":"rs1200800084","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["CCC","CC"],"end":140448877,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448875,"source":"dbSNP"},{"source":"dbSNP","start":140448877,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140448877,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1028683592","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1480358410","feature_type":"variation","strand":1,"end":140448878,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448878},{"clinical_significance":[],"id":"rs1799913400","seq_region_name":"7","source":"dbSNP","start":140448883,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140448883,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs10257079","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448884,"source":"dbSNP","strand":1,"feature_type":"variation","end":140448884,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs910902613","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448886,"source":"dbSNP","strand":1,"feature_type":"variation","end":140448886,"alleles":["G","A","C"]},{"source":"dbSNP","start":140448890,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140448890,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585453632"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799913536","feature_type":"variation","strand":1,"end":140448892,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448892},{"id":"rs1799913556","seq_region_name":"7","clinical_significance":[],"end":140448894,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140448894,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"strand":1,"feature_type":"variation","alleles":["AAAAAA","AAAAA"],"end":140448904,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448899,"source":"dbSNP","seq_region_name":"7","id":"rs1799913575","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448900,"feature_type":"variation","strand":1,"end":140448900,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs925002174"},{"seq_region_name":"7","id":"rs1799913624","clinical_significance":[],"alleles":["-","AAAACAACAGGCCGGG"],"end":140448904,"strand":1,"feature_type":"variation","start":140448905,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"end":140448905,"alleles":["-","GCAGTGGCTC"],"strand":1,"feature_type":"variation","start":140448906,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799913638","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448909,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140448909,"clinical_significance":[],"id":"rs1232349649","seq_region_name":"7"},{"end":140448910,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140448910,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs115329487","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448914,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140448914,"clinical_significance":[],"id":"rs1799913790","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799913812","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140448922,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448922},{"source":"dbSNP","start":140448923,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140448923,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1297655913"},{"source":"dbSNP","start":140448927,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140448927,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799913843"},{"seq_region_name":"7","id":"rs560587449","clinical_significance":[],"end":140448929,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140448929,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"id":"rs1799913878","seq_region_name":"7","feature_type":"variation","strand":1,"end":140448931,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448931},{"seq_region_name":"7","id":"rs1799913895","clinical_significance":[],"strand":1,"feature_type":"variation","end":140448935,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448935,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140448936,"alleles":["C","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448936,"clinical_significance":[],"seq_region_name":"7","id":"rs1799913916"},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140448939,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448939,"source":"dbSNP","seq_region_name":"7","id":"rs543643460","clinical_significance":[]},{"seq_region_name":"7","id":"rs1359944259","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448942,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AA","AAA"],"end":140448943},{"seq_region_name":"7","id":"rs987911741","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C","T"],"end":140448947,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448947,"source":"dbSNP"},{"end":140448947,"alleles":["G","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140448947,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1424836847"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448949,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140448949,"id":"rs1172286400","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs76465451","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140448950,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448950,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1353501176","source":"dbSNP","start":140448952,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140448952,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1375233545","seq_region_name":"7","feature_type":"variation","strand":1,"end":140448962,"alleles":["C","-"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448962},{"seq_region_name":"7","id":"rs1799914086","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448966,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140448966},{"alleles":["A","G"],"end":140448967,"feature_type":"variation","strand":1,"source":"dbSNP","start":140448967,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799914099"},{"alleles":["C","T"],"end":140448969,"feature_type":"variation","strand":1,"source":"dbSNP","start":140448969,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs935070179","seq_region_name":"7"},{"end":140448972,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140448972,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs949358205","clinical_significance":[]},{"start":140448974,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140448974,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1045366548","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs113769212","source":"dbSNP","start":140448975,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140448975,"alleles":["C","T"],"feature_type":"variation","strand":1},{"alleles":["CTCTC","CTC"],"end":140448979,"feature_type":"variation","strand":1,"source":"dbSNP","start":140448975,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799914210"},{"alleles":["T","C"],"end":140448976,"strand":1,"feature_type":"variation","start":140448976,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799914231","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs55751919","source":"dbSNP","start":140448978,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["TCATTCATT","TCATT","TCATTCATTCATT"],"end":140448986,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1443782751","clinical_significance":[],"start":140448979,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140448979,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140448980,"alleles":["A","C","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448980,"source":"dbSNP","seq_region_name":"7","id":"rs1052318854","clinical_significance":[]},{"id":"rs1585453697","seq_region_name":"7","clinical_significance":[],"start":140448981,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140448981,"strand":1,"feature_type":"variation"},{"alleles":["TT","T"],"end":140448982,"feature_type":"variation","strand":1,"source":"dbSNP","start":140448981,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1563082668","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1799914349","seq_region_name":"7","alleles":["C","A"],"end":140448983,"feature_type":"variation","strand":1,"source":"dbSNP","start":140448983,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140448983,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140448984,"alleles":["CA","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs200866947","seq_region_name":"7"},{"seq_region_name":"7","id":"rs200790273","clinical_significance":[],"strand":1,"feature_type":"variation","end":140448984,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448984,"source":"dbSNP"},{"end":140448986,"alleles":["ATT","-"],"strand":1,"feature_type":"variation","start":140448984,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1304039458","clinical_significance":[]},{"seq_region_name":"7","id":"rs896306555","clinical_significance":[],"start":140448986,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140448986,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1585453706","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140448988,"feature_type":"variation","strand":1,"end":140448988,"alleles":["G","A"]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140448989,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448989,"source":"dbSNP","seq_region_name":"7","id":"rs2130218177","clinical_significance":[]},{"end":140448990,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140448990,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1339857861"},{"source":"dbSNP","start":140448991,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140448991,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1013486107","seq_region_name":"7"},{"end":140448992,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140448992,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs546443188"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799914523","alleles":["A","G"],"end":140448996,"feature_type":"variation","strand":1,"source":"dbSNP","start":140448996,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140448997,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140448997,"source":"dbSNP","seq_region_name":"7","id":"rs185256184","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799914578","end":140448998,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140448998,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1278723385","end":140449001,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140449001,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449002,"source":"dbSNP","strand":1,"feature_type":"variation","end":140449002,"alleles":["G","T"],"seq_region_name":"7","id":"rs1293978928","clinical_significance":[]},{"alleles":["G","A"],"end":140449004,"feature_type":"variation","strand":1,"source":"dbSNP","start":140449004,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799914648"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140449005,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449005,"clinical_significance":[],"id":"rs1799914668","seq_region_name":"7"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449006,"feature_type":"variation","strand":1,"end":140449006,"alleles":["A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1001504854"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449009,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140449009,"seq_region_name":"7","id":"rs187481891","clinical_significance":[]},{"alleles":["G","C"],"end":140449012,"strand":1,"feature_type":"variation","start":140449012,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799914737","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449021,"feature_type":"variation","strand":1,"end":140449021,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799914761"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799914776","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449022,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140449022},{"seq_region_name":"7","id":"rs1271155189","clinical_significance":[],"end":140449031,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140449031,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140449035,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449035,"source":"dbSNP","id":"rs2130218242","seq_region_name":"7","clinical_significance":[]},{"end":140449053,"alleles":["CAGGTCATGATCAGGT","CAGGT"],"strand":1,"feature_type":"variation","start":140449038,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1333779012","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140449039,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449039,"source":"dbSNP","seq_region_name":"7","id":"rs1799914836","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449040,"feature_type":"variation","strand":1,"end":140449040,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799914851"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449045,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140449045,"seq_region_name":"7","id":"rs1041203930","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449046,"source":"dbSNP","strand":1,"feature_type":"variation","end":140449046,"alleles":["G","A"],"id":"rs1307100743","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140449052,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449052,"source":"dbSNP","seq_region_name":"7","id":"rs1210944414","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799914950","feature_type":"variation","strand":1,"end":140449058,"alleles":["GTGAGTG","GTG"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449052},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449056,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140449056,"clinical_significance":[],"id":"rs1465555495","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140449057,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449057,"clinical_significance":[],"seq_region_name":"7","id":"rs1799914989"},{"id":"rs1017340238","seq_region_name":"7","clinical_significance":[],"alleles":["G","T"],"end":140449063,"strand":1,"feature_type":"variation","start":140449063,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs532299212","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140449068,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449068,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1484714330","end":140449069,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140449069,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140449070,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140449070,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs997148933","seq_region_name":"7"},{"start":140449076,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","T"],"end":140449076,"strand":1,"feature_type":"variation","id":"rs1473501663","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","A"],"end":140449086,"strand":1,"feature_type":"variation","start":140449086,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1799915095","seq_region_name":"7","clinical_significance":[]},{"id":"rs1799915119","seq_region_name":"7","clinical_significance":[],"start":140449086,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","-"],"end":140449086,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1235338733","source":"dbSNP","start":140449089,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140449089,"alleles":["G","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1186439882","clinical_significance":[],"strand":1,"feature_type":"variation","end":140449092,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449092,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799915169","source":"dbSNP","start":140449101,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140449101,"feature_type":"variation","strand":1},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449105,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140449105,"clinical_significance":[],"seq_region_name":"7","id":"rs550535130"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1187957810","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449107,"feature_type":"variation","strand":1,"alleles":["TTTT","TTTTT"],"end":140449110},{"feature_type":"variation","strand":1,"end":140449113,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449113,"clinical_significance":[],"id":"rs973208348","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140449118,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449118,"clinical_significance":[],"id":"rs73485136","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1799915280","seq_region_name":"7","alleles":["A","C"],"end":140449122,"feature_type":"variation","strand":1,"source":"dbSNP","start":140449122,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449124,"feature_type":"variation","strand":1,"end":140449124,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799915294"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449132,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140449132,"seq_region_name":"7","id":"rs1196596961","clinical_significance":[]},{"seq_region_name":"7","id":"rs953084390","clinical_significance":[],"alleles":["T","A"],"end":140449134,"strand":1,"feature_type":"variation","start":140449134,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"end":140449141,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140449141,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs536393698"},{"end":140449143,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140449143,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1799915356","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140449145,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449145,"source":"dbSNP","seq_region_name":"7","id":"rs1479014311","clinical_significance":[]},{"end":140449147,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140449147,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1273748553","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs55833852","feature_type":"variation","strand":1,"end":140449156,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449156},{"clinical_significance":[],"seq_region_name":"7","id":"rs1032070312","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449157,"feature_type":"variation","strand":1,"end":140449157,"alleles":["G","A"]},{"end":140449162,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140449162,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799915543"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449164,"feature_type":"variation","strand":1,"end":140449164,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs776442077"},{"source":"dbSNP","start":140449165,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140449165,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799915577","seq_region_name":"7"},{"seq_region_name":"7","id":"rs771030276","clinical_significance":[],"start":140449167,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140449167,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1799915595","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140449170,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449170},{"clinical_significance":[],"seq_region_name":"7","id":"rs566832363","feature_type":"variation","strand":1,"end":140449171,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449171},{"seq_region_name":"7","id":"rs776528331","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140449172,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449172,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1283717435","seq_region_name":"7","source":"dbSNP","start":140449173,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140449173,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs942367027","source":"dbSNP","start":140449174,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140449174,"alleles":["A","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1337820038","clinical_significance":[],"start":140449176,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140449176,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449179,"source":"dbSNP","strand":1,"feature_type":"variation","end":140449179,"alleles":["T","A","C"],"seq_region_name":"7","id":"rs979157122","clinical_significance":[]},{"seq_region_name":"7","id":"rs1329729263","clinical_significance":[],"end":140449183,"alleles":["TTCT","T"],"strand":1,"feature_type":"variation","start":140449180,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"id":"rs1799915769","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449184,"source":"dbSNP","strand":1,"feature_type":"variation","end":140449184,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1356966439","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140449185,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449185,"source":"dbSNP"},{"id":"rs1799915809","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140449188,"strand":1,"feature_type":"variation","start":140449188,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"feature_type":"variation","strand":1,"end":140449196,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449196,"clinical_significance":[],"id":"rs1446515322","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1395783988","clinical_significance":[],"end":140449198,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140449198,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140449202,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449202,"clinical_significance":[],"id":"rs1799915882","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799915899","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449202,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","-"],"end":140449202},{"id":"rs769666764","seq_region_name":"7","clinical_significance":[],"alleles":["A","G"],"end":140449203,"strand":1,"feature_type":"variation","start":140449203,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"start":140449206,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140449206,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1298792593","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs970964628","alleles":["A","G"],"end":140449208,"feature_type":"variation","strand":1,"source":"dbSNP","start":140449208,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1799915990","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449222,"source":"dbSNP","strand":1,"feature_type":"variation","end":140449222,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs534190502","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140449227,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449227},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140449230,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449230,"source":"dbSNP","id":"rs1799916031","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1342227031","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449231,"source":"dbSNP","strand":1,"feature_type":"variation","end":140449231,"alleles":["G","A"]},{"clinical_significance":[],"id":"rs935121503","seq_region_name":"7","source":"dbSNP","start":140449232,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140449232,"feature_type":"variation","strand":1},{"end":140449236,"alleles":["CATC","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140449233,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1563082704","seq_region_name":"7"},{"end":140449234,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140449234,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799916118","clinical_significance":[]},{"end":140449236,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140449236,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1397949716","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799916170","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449238,"source":"dbSNP","strand":1,"feature_type":"variation","end":140449238,"alleles":["A","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799916189","source":"dbSNP","start":140449245,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140449245,"feature_type":"variation","strand":1},{"start":140449247,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140449247,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585453820","clinical_significance":[]},{"seq_region_name":"7","id":"rs1269330725","clinical_significance":[],"start":140449249,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140449249,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs559268202","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449251,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140449251},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449253,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140449253,"clinical_significance":[],"id":"rs1052122418","seq_region_name":"7"},{"seq_region_name":"7","id":"rs896337508","clinical_significance":[],"end":140449255,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140449255,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"start":140449256,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140449256,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130218551","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449257,"source":"dbSNP","strand":1,"feature_type":"variation","end":140449257,"alleles":["T","C"],"seq_region_name":"7","id":"rs1253502078","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799916299","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449258,"feature_type":"variation","strand":1,"alleles":["C","-"],"end":140449258},{"start":140449260,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140449260,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs772713959","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449261,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140449261,"seq_region_name":"7","id":"rs1220075825","clinical_significance":[]},{"id":"rs527411911","seq_region_name":"7","clinical_significance":[],"end":140449264,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140449264,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"end":140449267,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140449267,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1303671089","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130218568","clinical_significance":[],"alleles":["C","T"],"end":140449268,"strand":1,"feature_type":"variation","start":140449268,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799916411","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140449272,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449272},{"seq_region_name":"7","id":"rs980746243","clinical_significance":[],"strand":1,"feature_type":"variation","end":140449273,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449273,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1799916441","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140449282,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449282},{"seq_region_name":"7","id":"rs1799916459","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449283,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140449283},{"seq_region_name":"7","id":"rs1799916476","clinical_significance":[],"start":140449287,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","G"],"end":140449287,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140449289,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449289,"source":"dbSNP","seq_region_name":"7","id":"rs926497991","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140449296,"alleles":["C","G","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449296,"clinical_significance":[],"seq_region_name":"7","id":"rs577485482"},{"source":"dbSNP","start":140449303,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140449303,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs949198294","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1048401029","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140449305,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449305,"source":"dbSNP"},{"end":140449308,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140449308,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1287371594","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449315,"source":"dbSNP","strand":1,"feature_type":"variation","end":140449315,"alleles":["T","G"],"seq_region_name":"7","id":"rs1799916611","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799916637","alleles":["G","C"],"end":140449319,"feature_type":"variation","strand":1,"source":"dbSNP","start":140449319,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1295696490","clinical_significance":[],"strand":1,"feature_type":"variation","end":140449320,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449320,"source":"dbSNP"},{"clinical_significance":[],"id":"rs908639016","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449325,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140449325},{"seq_region_name":"7","id":"rs1349875476","clinical_significance":[],"start":140449328,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140449328,"strand":1,"feature_type":"variation"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449329,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140449329,"clinical_significance":[],"seq_region_name":"7","id":"rs1044964029"},{"seq_region_name":"7","id":"rs1322232127","clinical_significance":[],"end":140449330,"alleles":["A","C","T"],"strand":1,"feature_type":"variation","start":140449330,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"alleles":["TTTTT","TTTT"],"end":140449336,"feature_type":"variation","strand":1,"source":"dbSNP","start":140449332,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799916738"},{"clinical_significance":[],"id":"rs1400792516","seq_region_name":"7","source":"dbSNP","start":140449334,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140449334,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs905152186","clinical_significance":[],"start":140449337,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140449337,"strand":1,"feature_type":"variation"},{"alleles":["T","C"],"end":140449338,"feature_type":"variation","strand":1,"source":"dbSNP","start":140449338,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1041525595"},{"start":140449339,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","T"],"end":140449339,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799916806","clinical_significance":[]},{"end":140449340,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140449340,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1799916820","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799916837","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140449341,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449341,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799916856","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449342,"source":"dbSNP","strand":1,"feature_type":"variation","end":140449342,"alleles":["A","G"]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449342,"feature_type":"variation","strand":1,"alleles":["ATTCAGATCTCAATTCA","ATTCA"],"end":140449358,"clinical_significance":[],"id":"rs1438736217","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449343,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140449343,"seq_region_name":"7","id":"rs544777794","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799916898","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140449347,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449347},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140449349,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449349,"clinical_significance":[],"seq_region_name":"7","id":"rs1395436676"},{"feature_type":"variation","strand":1,"alleles":["C","A","G"],"end":140449350,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449350,"clinical_significance":[],"id":"rs769843995","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799916968","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449360,"feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140449360},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449372,"source":"dbSNP","strand":1,"feature_type":"variation","end":140449372,"alleles":["T","C"],"seq_region_name":"7","id":"rs373303521","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799917010","source":"dbSNP","start":140449379,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140449379,"alleles":["A","AA"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140449383,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140449383,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs2130218697","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799917035","clinical_significance":[],"strand":1,"feature_type":"variation","end":140449385,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449385,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1214117197","source":"dbSNP","start":140449387,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140449387,"alleles":["A","C"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140449388,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449388,"clinical_significance":[],"seq_region_name":"7","id":"rs1246063606"},{"source":"dbSNP","start":140449389,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140449389,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs898476732"},{"end":140449390,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140449390,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1241946079","seq_region_name":"7"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449391,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140449391,"clinical_significance":[],"id":"rs994275220","seq_region_name":"7"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449396,"feature_type":"variation","strand":1,"end":140449396,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1284101365"},{"id":"rs375315102","seq_region_name":"7","clinical_significance":[],"start":140449398,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140449398,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs955526569","clinical_significance":[],"strand":1,"feature_type":"variation","end":140449399,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449399,"source":"dbSNP"},{"alleles":["G","A"],"end":140449403,"feature_type":"variation","strand":1,"source":"dbSNP","start":140449403,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130218735"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449406,"source":"dbSNP","strand":1,"feature_type":"variation","end":140449406,"alleles":["G","C"],"seq_region_name":"7","id":"rs1799917221","clinical_significance":[]},{"seq_region_name":"7","id":"rs556524829","clinical_significance":[],"start":140449418,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140449418,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449427,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140449427,"seq_region_name":"7","id":"rs7789557","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1000501794","feature_type":"variation","strand":1,"end":140449430,"alleles":["A","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449430},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449432,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140449432,"clinical_significance":[],"seq_region_name":"7","id":"rs1799917448"},{"end":140449433,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140449433,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs370185757"},{"seq_region_name":"7","id":"rs1799917494","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["-","T"],"end":140449443,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449444,"source":"dbSNP"},{"seq_region_name":"7","id":"rs751117413","clinical_significance":[],"alleles":["A","G"],"end":140449445,"strand":1,"feature_type":"variation","start":140449445,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"source":"dbSNP","start":140449447,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140449447,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799917541","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799917557","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140449451,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449451,"source":"dbSNP"},{"source":"dbSNP","start":140449452,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140449452,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1361858469"},{"end":140449456,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140449456,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs980077202"},{"clinical_significance":[],"id":"rs1158683692","seq_region_name":"7","source":"dbSNP","start":140449460,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140449460,"feature_type":"variation","strand":1},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449463,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140449463,"clinical_significance":[],"seq_region_name":"7","id":"rs1563082749"},{"seq_region_name":"7","id":"rs1375758746","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449472,"source":"dbSNP","strand":1,"feature_type":"variation","end":140449483,"alleles":["CAAAACAAAATC","-"]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140449477,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449477,"source":"dbSNP","seq_region_name":"7","id":"rs1799917667","clinical_significance":[]},{"id":"rs1362405827","seq_region_name":"7","clinical_significance":[],"end":140449480,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140449480,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449482,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140449482,"seq_region_name":"7","id":"rs1799917703","clinical_significance":[]},{"id":"rs1799917720","seq_region_name":"7","clinical_significance":[],"start":140449483,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140449483,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs925004074","seq_region_name":"7","source":"dbSNP","start":140449490,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140449490,"alleles":["A","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1431246026","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449497,"feature_type":"variation","strand":1,"alleles":["TTT","TT"],"end":140449499},{"end":140449500,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","start":140449500,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs956545464","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140449501,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140449501,"alleles":["T","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799917790","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1424317328","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449502,"feature_type":"variation","strand":1,"end":140449502,"alleles":["C","T"]},{"alleles":["TT","-"],"end":140449506,"strand":1,"feature_type":"variation","start":140449505,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs368179265","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449506,"feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140449506,"clinical_significance":[],"seq_region_name":"7","id":"rs1317517248"},{"strand":1,"feature_type":"variation","end":140449507,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449507,"source":"dbSNP","seq_region_name":"7","id":"rs1799917881","clinical_significance":[]},{"source":"dbSNP","start":140449512,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140449512,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs987869174"},{"seq_region_name":"7","id":"rs1261098044","clinical_significance":[],"alleles":["C","A"],"end":140449514,"strand":1,"feature_type":"variation","start":140449514,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449515,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140449515,"clinical_significance":[],"id":"rs1193121982","seq_region_name":"7"},{"start":140449521,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","A","C"],"end":140449521,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs917628373","clinical_significance":[]},{"alleles":["G","A"],"end":140449529,"feature_type":"variation","strand":1,"source":"dbSNP","start":140449529,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799917977","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1009310003","alleles":["G","A"],"end":140449532,"feature_type":"variation","strand":1,"source":"dbSNP","start":140449532,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449534,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140449534,"clinical_significance":[],"seq_region_name":"7","id":"rs1025134557"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449536,"feature_type":"variation","strand":1,"end":140449536,"alleles":["G","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130218887"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1208392905","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140449537,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449537},{"id":"rs1799918071","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449538,"source":"dbSNP","strand":1,"feature_type":"variation","end":140449538,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1799918091","clinical_significance":[],"start":140449539,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140449539,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585453923","source":"dbSNP","start":140449543,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140449543,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs949230895","clinical_significance":[],"alleles":["T","C"],"end":140449548,"strand":1,"feature_type":"variation","start":140449548,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"id":"rs760061805","seq_region_name":"7","source":"dbSNP","start":140449551,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140449551,"alleles":["C","G"],"feature_type":"variation","strand":1},{"start":140449554,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140449554,"strand":1,"feature_type":"variation","id":"rs1044913830","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1438332390","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449555,"source":"dbSNP","strand":1,"feature_type":"variation","end":140449555,"alleles":["G","A"]},{"alleles":["A","G"],"end":140449556,"strand":1,"feature_type":"variation","start":140449556,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1220976052","clinical_significance":[]},{"start":140449556,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["ACACA","ACA"],"end":140449560,"strand":1,"feature_type":"variation","id":"rs763436408","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140449562,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449562,"source":"dbSNP","seq_region_name":"7","id":"rs1339172283","clinical_significance":[]},{"seq_region_name":"7","id":"rs1275756580","clinical_significance":[],"alleles":["G","T"],"end":140449563,"strand":1,"feature_type":"variation","start":140449563,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"end":140449570,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140449570,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs970591991","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140449572,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449572,"clinical_significance":[],"seq_region_name":"7","id":"rs926430349"},{"id":"rs1799918317","seq_region_name":"7","clinical_significance":[],"start":140449573,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140449573,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799918332","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449579,"feature_type":"variation","strand":1,"end":140449579,"alleles":["T","C"]},{"alleles":["G","C"],"end":140449580,"feature_type":"variation","strand":1,"source":"dbSNP","start":140449580,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs941986504","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449582,"source":"dbSNP","strand":1,"feature_type":"variation","end":140449582,"alleles":["C","T"],"seq_region_name":"7","id":"rs1799918357","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799918378","end":140449583,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140449583,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140449588,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449588,"clinical_significance":[],"id":"rs1799918389","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799918405","clinical_significance":[],"start":140449589,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140449592,"alleles":["CTCT","CT"],"strand":1,"feature_type":"variation"},{"id":"rs1799918424","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449590,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140449590},{"source":"dbSNP","start":140449592,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140449592,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1033619822","seq_region_name":"7"},{"end":140449593,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140449593,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799918468","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140449597,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449597,"clinical_significance":[],"id":"rs1799918481","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1799918507","seq_region_name":"7","source":"dbSNP","start":140449604,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140449604,"alleles":["A","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799918524","end":140449606,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140449606,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1037993084","source":"dbSNP","start":140449615,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140449615,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs542271259","clinical_significance":[],"start":140449623,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","A","T"],"end":140449623,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585453961","feature_type":"variation","strand":1,"end":140449625,"alleles":["T","C","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449625},{"end":140449631,"alleles":["ACA","A"],"strand":1,"feature_type":"variation","start":140449629,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799918601","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799918619","alleles":["AGAGA","AGA"],"end":140449635,"feature_type":"variation","strand":1,"source":"dbSNP","start":140449631,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1799918636","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449632,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140449632},{"start":140449634,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140449634,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799918652","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1467114358","source":"dbSNP","start":140449636,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140449636,"feature_type":"variation","strand":1},{"start":140449637,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140449637,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs148247248","clinical_significance":[]},{"end":140449638,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140449638,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1799918731","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799918746","clinical_significance":[],"strand":1,"feature_type":"variation","end":140449643,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449643,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449644,"source":"dbSNP","strand":1,"feature_type":"variation","end":140449643,"alleles":["-","TC"],"seq_region_name":"7","id":"rs1563082773","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140449644,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449644,"source":"dbSNP","seq_region_name":"7","id":"rs1799918782","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140449646,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449646,"clinical_significance":[],"seq_region_name":"7","id":"rs952577569"},{"end":140449648,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140449648,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799918818"},{"clinical_significance":[],"seq_region_name":"7","id":"rs994127293","end":140449649,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140449649,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"end":140449650,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140449650,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799918855","seq_region_name":"7"},{"alleles":["C","T"],"end":140449653,"strand":1,"feature_type":"variation","start":140449653,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1047184466","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140449653,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","CC"],"end":140449653,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1475589497"},{"clinical_significance":[],"seq_region_name":"7","id":"rs891248237","feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140449655,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449655},{"seq_region_name":"7","id":"rs753066161","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140449656,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449656,"source":"dbSNP"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449657,"feature_type":"variation","strand":1,"end":140449657,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1233800583"},{"feature_type":"variation","strand":1,"end":140449658,"alleles":["C","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449658,"clinical_significance":[],"seq_region_name":"7","id":"rs1200993072"},{"seq_region_name":"7","id":"rs1799918991","clinical_significance":[],"start":140449662,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140449662,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140449663,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449663,"clinical_significance":[],"seq_region_name":"7","id":"rs1316527739"},{"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140449665,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449665,"clinical_significance":[],"seq_region_name":"7","id":"rs756412843"},{"clinical_significance":[],"id":"rs984024159","seq_region_name":"7","end":140449666,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140449666,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"alleles":["T","TT"],"end":140449667,"feature_type":"variation","strand":1,"source":"dbSNP","start":140449667,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1222599459"},{"clinical_significance":[],"id":"rs1794293058","seq_region_name":"7","source":"dbSNP","start":140449668,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140449668,"feature_type":"variation","strand":1},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449668,"feature_type":"variation","strand":1,"alleles":["GAG","G"],"end":140449670,"clinical_significance":[],"seq_region_name":"7","id":"rs1794293089"},{"source":"dbSNP","start":140449671,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140449671,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1018479109"},{"source":"dbSNP","start":140449676,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140449676,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794293149"},{"end":140449677,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140449677,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1794293175","clinical_significance":[]},{"start":140449678,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140449678,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs796551896","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140449679,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449679,"clinical_significance":[],"seq_region_name":"7","id":"rs1794293241"},{"seq_region_name":"7","id":"rs1794293270","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140449680,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449680,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1794293297","clinical_significance":[],"strand":1,"feature_type":"variation","end":140449681,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449681,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449683,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140449683,"seq_region_name":"7","id":"rs1794293330","clinical_significance":[]},{"clinical_significance":[],"id":"rs939996517","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140449685,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449685},{"clinical_significance":[],"id":"rs1378069801","seq_region_name":"7","alleles":["C","T"],"end":140449686,"feature_type":"variation","strand":1,"source":"dbSNP","start":140449686,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140449691,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449691,"clinical_significance":[],"seq_region_name":"7","id":"rs976871900"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794293463","feature_type":"variation","strand":1,"end":140449708,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449708},{"source":"dbSNP","start":140449713,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140449713,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs964548580"},{"source":"dbSNP","start":140449714,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140449714,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794293531"},{"id":"rs922639265","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140449718,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449718,"source":"dbSNP"},{"source":"dbSNP","start":140449722,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140449722,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1585454010","seq_region_name":"7"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449727,"feature_type":"variation","strand":1,"end":140449727,"alleles":["T","C"],"clinical_significance":[],"id":"rs1397963866","seq_region_name":"7"},{"id":"rs1169915989","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449728,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GGG","GG"],"end":140449730},{"seq_region_name":"7","id":"rs1458380285","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449729,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140449729},{"seq_region_name":"7","id":"rs1001139686","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449734,"source":"dbSNP","strand":1,"feature_type":"variation","end":140449734,"alleles":["G","A","C"]},{"seq_region_name":"7","id":"rs1794293732","clinical_significance":[],"end":140449740,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140449740,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"end":140449746,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140449746,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1032983179"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1050323290","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449750,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140449750},{"seq_region_name":"7","id":"rs1452603419","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449753,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140449753},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449755,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140449755,"clinical_significance":[],"id":"rs528048141","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585454033","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449756,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140449756},{"start":140449757,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140449757,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1250788892","clinical_significance":[]},{"clinical_significance":[],"id":"rs1224160998","seq_region_name":"7","end":140449761,"alleles":["TGTGT","TGT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140449757,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140449758,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140449758,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1408994068"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794294002","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449760,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140449760},{"end":140449766,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140449766,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs372456234","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1436169964","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140449767,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449767,"source":"dbSNP"},{"source":"dbSNP","start":140449768,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140449768,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs904688706"},{"feature_type":"variation","strand":1,"end":140449769,"alleles":["A","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449769,"clinical_significance":[],"id":"rs764744732","seq_region_name":"7"},{"alleles":["T","C"],"end":140449779,"feature_type":"variation","strand":1,"source":"dbSNP","start":140449779,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1456733770","seq_region_name":"7"},{"id":"rs1238065171","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449781,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140449781},{"start":140449785,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","TT"],"end":140449785,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs936282108","clinical_significance":[]},{"end":140449786,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140449786,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1489784439"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794294377","alleles":["A","G"],"end":140449789,"feature_type":"variation","strand":1,"source":"dbSNP","start":140449789,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"start":140449790,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","G"],"end":140449790,"strand":1,"feature_type":"variation","id":"rs2130219204","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1381673697","source":"dbSNP","start":140449791,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140449791,"alleles":["A","G"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140449792,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449792,"clinical_significance":[],"seq_region_name":"7","id":"rs141303087"},{"id":"rs1794294499","seq_region_name":"7","clinical_significance":[],"start":140449793,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140449793,"alleles":["T","G"],"strand":1,"feature_type":"variation"},{"id":"rs1794294521","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140449806,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449806,"source":"dbSNP"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449809,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140449809,"clinical_significance":[],"seq_region_name":"7","id":"rs1794294543"},{"clinical_significance":[],"id":"rs2130219229","seq_region_name":"7","source":"dbSNP","start":140449817,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140449817,"alleles":["T","TTTT"],"feature_type":"variation","strand":1},{"alleles":["C","G","T"],"end":140449820,"strand":1,"feature_type":"variation","start":140449820,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1794294579","clinical_significance":[]},{"id":"rs987734465","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140449822,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449822,"source":"dbSNP"},{"end":140449827,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140449827,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs565170354","seq_region_name":"7"},{"start":140449831,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140449831,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794294675","clinical_significance":[]},{"end":140449837,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140449837,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs2130219249","seq_region_name":"7"},{"seq_region_name":"7","id":"rs917579290","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449838,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","G"],"end":140449838},{"clinical_significance":[],"seq_region_name":"7","id":"rs1309556273","feature_type":"variation","strand":1,"end":140449841,"alleles":["T","C","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449841},{"id":"rs1794294764","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449843,"source":"dbSNP","strand":1,"feature_type":"variation","end":140449843,"alleles":["A","G"]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449849,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140449849,"seq_region_name":"7","id":"rs892163721","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794294832","source":"dbSNP","start":140449851,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140449851,"alleles":["A","G"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140449855,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449855,"source":"dbSNP","seq_region_name":"7","id":"rs1009610155","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140449858,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449858,"source":"dbSNP","seq_region_name":"7","id":"rs532330860","clinical_significance":[]},{"id":"rs1794294901","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140449859,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449859,"source":"dbSNP"},{"end":140449862,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140449862,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1794294924","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1024726627","end":140449864,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140449864,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449867,"feature_type":"variation","strand":1,"alleles":["AA","AAAA"],"end":140449868,"clinical_significance":[],"seq_region_name":"7","id":"rs1414366780"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130219302","feature_type":"variation","strand":1,"end":140449870,"alleles":["ACA","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449868},{"id":"rs906251247","seq_region_name":"7","clinical_significance":[],"start":140449869,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","G"],"end":140449869,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140449880,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449880,"clinical_significance":[],"seq_region_name":"7","id":"rs754003239"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449881,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140449881,"seq_region_name":"7","id":"rs192396389","clinical_significance":[]},{"start":140449884,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","A","T"],"end":140449884,"strand":1,"feature_type":"variation","id":"rs1457482468","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449885,"source":"dbSNP","strand":1,"feature_type":"variation","end":140449885,"alleles":["G","A","C"],"seq_region_name":"7","id":"rs1794295085","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449889,"source":"dbSNP","strand":1,"feature_type":"variation","end":140449889,"alleles":["T","C"],"seq_region_name":"7","id":"rs1794295101","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140449898,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449898,"source":"dbSNP","id":"rs1794295122","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["CTCAGCACTTTG","-"],"end":140449913,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449902,"clinical_significance":[],"id":"rs1794295142","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794295162","feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140449903,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449903},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794295181","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449906,"feature_type":"variation","strand":1,"alleles":["GCACTT","GCACTTGCACTT"],"end":140449911},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130219342","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140449911,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449911},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140449917,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449917,"clinical_significance":[],"id":"rs980475680","seq_region_name":"7"},{"alleles":["G","T"],"end":140449918,"strand":1,"feature_type":"variation","start":140449918,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1440506270","clinical_significance":[]},{"alleles":["A","G"],"end":140449921,"feature_type":"variation","strand":1,"source":"dbSNP","start":140449921,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1794295241","seq_region_name":"7"},{"start":140449925,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","T"],"end":140449925,"strand":1,"feature_type":"variation","id":"rs1794295253","seq_region_name":"7","clinical_significance":[]},{"start":140449927,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140449927,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794295268","clinical_significance":[]},{"seq_region_name":"7","id":"rs1160714001","clinical_significance":[],"end":140449965,"alleles":["CTGAGGTCAGGAGTTCCAGGCTGAGGTCAGGAGTTCCAG","CTGAGGTCAGGAGTTCCAG","CTGAGGTCAGGAGTTCCAGGCTGAGGTCAGGAGTTCCAGGCTGAGGTCAGGAGTTCCAG"],"strand":1,"feature_type":"variation","start":140449927,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"strand":1,"feature_type":"variation","end":140449931,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449931,"source":"dbSNP","seq_region_name":"7","id":"rs1379290129","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449932,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140449932,"clinical_significance":[],"seq_region_name":"7","id":"rs1794295331"},{"end":140449934,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140449934,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585454080"},{"strand":1,"feature_type":"variation","end":140449939,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449939,"source":"dbSNP","seq_region_name":"7","id":"rs1380056577","clinical_significance":[]},{"id":"rs1794295379","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140449946,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449946,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1440091708","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449947,"source":"dbSNP","strand":1,"feature_type":"variation","end":140449947,"alleles":["C","T"]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449948,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140449948,"seq_region_name":"7","id":"rs1033540946","clinical_significance":[]},{"source":"dbSNP","start":140449951,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140449951,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs952504355"},{"source":"dbSNP","start":140449954,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140449954,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1279499385"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449955,"source":"dbSNP","strand":1,"feature_type":"variation","end":140449955,"alleles":["A","G"],"seq_region_name":"7","id":"rs926490429","clinical_significance":[]},{"end":140449956,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140449956,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1487889232","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449957,"source":"dbSNP","strand":1,"feature_type":"variation","end":140449957,"alleles":["G","A"],"id":"rs1230412236","seq_region_name":"7","clinical_significance":[]},{"start":140449960,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140449960,"alleles":["T","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794295552","clinical_significance":[]},{"id":"rs1271723273","seq_region_name":"7","clinical_significance":[],"start":140449961,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","A"],"end":140449961,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs2130219415","clinical_significance":[],"strand":1,"feature_type":"variation","end":140449962,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449962,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449964,"source":"dbSNP","strand":1,"feature_type":"variation","end":140449964,"alleles":["A","G"],"seq_region_name":"7","id":"rs11773037","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1198959372","feature_type":"variation","strand":1,"end":140449967,"alleles":["C","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449967},{"clinical_significance":[],"seq_region_name":"7","id":"rs7805365","source":"dbSNP","start":140449968,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140449968,"alleles":["T","A","C"],"feature_type":"variation","strand":1},{"end":140449969,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140449969,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs919133721"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1435584264","source":"dbSNP","start":140449970,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140449970,"alleles":["G","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1332699608","clinical_significance":[],"strand":1,"feature_type":"variation","end":140449975,"alleles":["GG","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449974,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449976,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140449976,"seq_region_name":"7","id":"rs1299135065","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140449977,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449977,"clinical_significance":[],"id":"rs929197928","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140449980,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449980,"source":"dbSNP","id":"rs745972733","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1238013690","seq_region_name":"7","source":"dbSNP","start":140449982,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","A","C"],"end":140449982,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1794295997","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140449983,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449983,"source":"dbSNP"},{"end":140449985,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140449985,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs866667026","seq_region_name":"7"},{"clinical_significance":[],"id":"rs891115602","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140449986,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449986},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130219521","feature_type":"variation","strand":1,"alleles":["T","A"],"end":140449988,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449988},{"alleles":["T","C"],"end":140449990,"strand":1,"feature_type":"variation","start":140449990,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1794296051","seq_region_name":"7","clinical_significance":[]},{"id":"rs1418087958","seq_region_name":"7","clinical_significance":[],"end":140449991,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140449991,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140449993,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140449993,"id":"rs9692138","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs184592419","clinical_significance":[],"alleles":["G","A","C"],"end":140449994,"strand":1,"feature_type":"variation","start":140449994,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140449998,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140449998,"clinical_significance":[],"seq_region_name":"7","id":"rs534150377"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1001402578","source":"dbSNP","start":140450002,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140450002,"alleles":["T","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794296196","source":"dbSNP","start":140450005,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140450005,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1794296209","clinical_significance":[],"start":140450006,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140450006,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"alleles":["A","T"],"end":140450007,"strand":1,"feature_type":"variation","start":140450007,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1794296217","seq_region_name":"7","clinical_significance":[]},{"end":140450010,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140450010,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs2130219582","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140450011,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450011,"source":"dbSNP","seq_region_name":"7","id":"rs1032605004","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs552639911","source":"dbSNP","start":140450014,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140450014,"alleles":["A","C"],"feature_type":"variation","strand":1},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450019,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140450019,"clinical_significance":[],"seq_region_name":"7","id":"rs1198735171"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450020,"feature_type":"variation","strand":1,"end":140450020,"alleles":["C","T"],"clinical_significance":[],"id":"rs1478462773","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140450022,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450022,"clinical_significance":[],"seq_region_name":"7","id":"rs1794296333"},{"seq_region_name":"7","id":"rs571119470","clinical_significance":[],"start":140450023,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140450023,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1263257036","source":"dbSNP","start":140450023,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["GGCGTCATGGTTGGCG","GGCG"],"end":140450038,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1009755314","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450024,"feature_type":"variation","strand":1,"alleles":["G","C","T"],"end":140450024},{"clinical_significance":[],"seq_region_name":"7","id":"rs368986630","feature_type":"variation","strand":1,"end":140450025,"alleles":["C","G","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450025},{"clinical_significance":[],"id":"rs1794298969","seq_region_name":"7","feature_type":"variation","strand":1,"end":140450028,"alleles":["CGTC","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450025},{"clinical_significance":[],"seq_region_name":"7","id":"rs1328212028","source":"dbSNP","start":140450026,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140450026,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450031,"source":"dbSNP","strand":1,"feature_type":"variation","end":140450031,"alleles":["G","C"],"seq_region_name":"7","id":"rs1585454156","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140450032,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450032,"clinical_significance":[],"seq_region_name":"7","id":"rs1254068796"},{"clinical_significance":[],"id":"rs1232419640","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450033,"feature_type":"variation","strand":1,"end":140450033,"alleles":["T","C"]},{"start":140450034,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140450034,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs1794299131","seq_region_name":"7","clinical_significance":[]},{"end":140450037,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140450037,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1341123956","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs970337879","end":140450038,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140450038,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140450042,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140450042,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1794299223","seq_region_name":"7"},{"alleles":["T","TT"],"end":140450043,"feature_type":"variation","strand":1,"source":"dbSNP","start":140450043,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1398237905"},{"clinical_significance":[],"seq_region_name":"7","id":"rs140366451","source":"dbSNP","start":140450047,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140450047,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs755794061","feature_type":"variation","strand":1,"end":140450051,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450051},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450053,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140450053,"clinical_significance":[],"seq_region_name":"7","id":"rs1335136531"},{"alleles":["C","T"],"end":140450055,"feature_type":"variation","strand":1,"source":"dbSNP","start":140450055,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1398044769"},{"seq_region_name":"7","id":"rs1400482291","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450059,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140450059},{"alleles":["T","C"],"end":140450075,"feature_type":"variation","strand":1,"source":"dbSNP","start":140450075,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs980506870"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794299453","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450081,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140450081},{"strand":1,"feature_type":"variation","end":140450086,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450086,"source":"dbSNP","seq_region_name":"7","id":"rs1794299473","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140450088,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450088,"source":"dbSNP","seq_region_name":"7","id":"rs1794299499","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794299531","clinical_significance":[],"alleles":["G","C"],"end":140450089,"strand":1,"feature_type":"variation","start":140450089,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1466597466","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450090,"source":"dbSNP","strand":1,"feature_type":"variation","end":140450090,"alleles":["A","T"]},{"seq_region_name":"7","id":"rs1426414759","clinical_significance":[],"strand":1,"feature_type":"variation","end":140450091,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450091,"source":"dbSNP"},{"id":"rs1033805320","seq_region_name":"7","clinical_significance":[],"end":140450092,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140450092,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450093,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140450093,"id":"rs963248675","seq_region_name":"7","clinical_significance":[]},{"id":"rs1476568350","seq_region_name":"7","clinical_significance":[],"start":140450094,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140450094,"alleles":["A","AA"],"strand":1,"feature_type":"variation"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450094,"feature_type":"variation","strand":1,"end":140450094,"alleles":["A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794302486"},{"source":"dbSNP","start":140450095,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C","G"],"end":140450095,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs973677954"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585454182","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450098,"feature_type":"variation","strand":1,"end":140450098,"alleles":["G","T"]},{"seq_region_name":"7","id":"rs1291979368","clinical_significance":[],"start":140450099,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140450099,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs919092619","end":140450101,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140450101,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"end":140450108,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140450108,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1794302593","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450110,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140450110,"seq_region_name":"7","id":"rs929233687","clinical_significance":[]},{"seq_region_name":"7","id":"rs1253806092","clinical_significance":[],"start":140450111,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140450111,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"alleles":["G","A","T"],"end":140450113,"strand":1,"feature_type":"variation","start":140450113,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1202875191","clinical_significance":[]},{"end":140450115,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","start":140450115,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs906184972","clinical_significance":[]},{"id":"rs1216828893","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450117,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140450117},{"source":"dbSNP","start":140450120,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140450120,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1794302720","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs556821971","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140450123,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450123},{"end":140450124,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140450124,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1002384277"},{"end":140450129,"alleles":["T","TT"],"strand":1,"feature_type":"variation","start":140450129,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1794302773","seq_region_name":"7","clinical_significance":[]},{"id":"rs1450448145","seq_region_name":"7","clinical_significance":[],"end":140450136,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140450136,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"source":"dbSNP","start":140450138,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140450138,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1338994284"},{"source":"dbSNP","start":140450139,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140450139,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs574886147","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1259597719","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450141,"source":"dbSNP","strand":1,"feature_type":"variation","end":140450141,"alleles":["G","A","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1447998580","alleles":["G","C"],"end":140450145,"feature_type":"variation","strand":1,"source":"dbSNP","start":140450145,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130219811","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140450147,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450147},{"feature_type":"variation","strand":1,"end":140450148,"alleles":["C","G","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450148,"clinical_significance":[],"id":"rs1794302881","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140450156,"alleles":["CTCT","CT"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450153,"clinical_significance":[],"seq_region_name":"7","id":"rs1054875063"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1194755351","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450154,"feature_type":"variation","strand":1,"end":140450154,"alleles":["T","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794302944","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450156,"feature_type":"variation","strand":1,"end":140450156,"alleles":["T","TT"]},{"feature_type":"variation","strand":1,"end":140450158,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450158,"clinical_significance":[],"id":"rs1278770750","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140450160,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450160,"source":"dbSNP","seq_region_name":"7","id":"rs1794302982","clinical_significance":[]},{"id":"rs1443609469","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450161,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140450161},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450163,"source":"dbSNP","strand":1,"feature_type":"variation","end":140450163,"alleles":["G","A"],"seq_region_name":"7","id":"rs75426147","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450163,"feature_type":"variation","strand":1,"end":140450164,"alleles":["GG","GGG"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794303036"},{"source":"dbSNP","start":140450164,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["-","A"],"end":140450163,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794303062"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1320626707","source":"dbSNP","start":140450164,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140450164,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140450165,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450165,"source":"dbSNP","seq_region_name":"7","id":"rs76956841","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs34359208","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450165,"feature_type":"variation","strand":1,"alleles":["AAAAAAAAAAAAAAA","AAAAAAAAAAA","AAAAAAAAAAAA","AAAAAAAAAAAAA","AAAAAAAAAAAAAA","AAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAA"],"end":140450179},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450167,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["-","T"],"end":140450166,"seq_region_name":"7","id":"rs1185801311","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450167,"feature_type":"variation","strand":1,"end":140450167,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1256696746"},{"id":"rs530867561","seq_region_name":"7","clinical_significance":[],"alleles":["A","C"],"end":140450171,"strand":1,"feature_type":"variation","start":140450171,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1196648776","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140450173,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450173},{"end":140450173,"alleles":["-","G"],"strand":1,"feature_type":"variation","start":140450174,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs72230629","seq_region_name":"7","clinical_significance":[]},{"id":"rs1794303321","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140450174,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450174,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794303344","alleles":["A","G"],"end":140450175,"feature_type":"variation","strand":1,"source":"dbSNP","start":140450175,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs888288937","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450176,"source":"dbSNP","strand":1,"feature_type":"variation","end":140450175,"alleles":["-","G"]},{"start":140450178,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140450178,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1005351043","clinical_significance":[]},{"start":140450179,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140450179,"alleles":["A","T"],"strand":1,"feature_type":"variation","id":"rs1794303405","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","TT"],"end":140450180,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450180,"source":"dbSNP","seq_region_name":"7","id":"rs1195490499","clinical_significance":[]},{"seq_region_name":"7","id":"rs1375031357","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A","C","G"],"end":140450180,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450180,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1794303422","clinical_significance":[],"start":140450183,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140450183,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"alleles":["A","G"],"end":140450185,"strand":1,"feature_type":"variation","start":140450185,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1585454268","clinical_significance":[]},{"alleles":["A","G"],"end":140450187,"strand":1,"feature_type":"variation","start":140450187,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs535674395","clinical_significance":[]},{"source":"dbSNP","start":140450188,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140450188,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1241280883","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794303496","source":"dbSNP","start":140450189,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140450189,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140450191,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450191,"source":"dbSNP","seq_region_name":"7","id":"rs554210388","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450192,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140450192,"id":"rs572635340","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140450193,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140450193,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1446683775"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794303598","source":"dbSNP","start":140450195,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140450195,"feature_type":"variation","strand":1},{"alleles":["T","C"],"end":140450200,"strand":1,"feature_type":"variation","start":140450200,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1039793806","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140450201,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450201,"clinical_significance":[],"seq_region_name":"7","id":"rs899881639"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450207,"feature_type":"variation","strand":1,"end":140450207,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1323571384"},{"id":"rs1794303674","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140450208,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450208,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450209,"source":"dbSNP","strand":1,"feature_type":"variation","end":140450209,"alleles":["A","G"],"seq_region_name":"7","id":"rs936762288","clinical_significance":[]},{"alleles":["AAAAA","AAAAAA"],"end":140450213,"feature_type":"variation","strand":1,"source":"dbSNP","start":140450209,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1406618450"},{"source":"dbSNP","start":140450210,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140450210,"alleles":["A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1388078242"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794303793","feature_type":"variation","strand":1,"end":140450217,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450217},{"clinical_significance":[],"seq_region_name":"7","id":"rs1162497900","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140450218,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450218},{"end":140450221,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140450221,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1439969038","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs189376276","source":"dbSNP","start":140450223,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140450223,"alleles":["C","G","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs564776412","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450224,"feature_type":"variation","strand":1,"end":140450224,"alleles":["G","A","C"]},{"source":"dbSNP","start":140450228,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140450228,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585454309"},{"seq_region_name":"7","id":"rs1794303935","clinical_significance":[],"end":140450230,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140450230,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"alleles":["C","T"],"end":140450231,"strand":1,"feature_type":"variation","start":140450231,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1009787512","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs577059431","source":"dbSNP","start":140450232,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140450232,"alleles":["G","A"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450234,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140450234,"id":"rs2130220025","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs372434613","feature_type":"variation","strand":1,"end":140450235,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450235},{"id":"rs1291185329","seq_region_name":"7","clinical_significance":[],"end":140450236,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140450236,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs2130220039","clinical_significance":[],"strand":1,"feature_type":"variation","end":140450238,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450238,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450239,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140450239,"seq_region_name":"7","id":"rs1401026298","clinical_significance":[]},{"id":"rs906209074","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450240,"source":"dbSNP","strand":1,"feature_type":"variation","end":140450240,"alleles":["G","C"]},{"clinical_significance":[],"id":"rs1794304078","seq_region_name":"7","source":"dbSNP","start":140450241,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140450241,"alleles":["T","C"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140450244,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450244,"clinical_significance":[],"seq_region_name":"7","id":"rs1794304100"},{"alleles":["C","G"],"end":140450245,"strand":1,"feature_type":"variation","start":140450245,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1356193565","seq_region_name":"7","clinical_significance":[]},{"end":140450246,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140450246,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs552748933","seq_region_name":"7"},{"end":140450250,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140450250,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1794304140","clinical_significance":[]},{"source":"dbSNP","start":140450255,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140450255,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1002240369"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1280434607","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450257,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140450257},{"clinical_significance":[],"seq_region_name":"7","id":"rs1325024656","source":"dbSNP","start":140450262,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140450262,"alleles":["C","A"],"feature_type":"variation","strand":1},{"start":140450264,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140450264,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1368851537","clinical_significance":[]},{"source":"dbSNP","start":140450265,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["AGGCAGG","AGGCAGGCAGG"],"end":140450271,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794304223"},{"id":"rs2130220083","seq_region_name":"7","clinical_significance":[],"end":140450266,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140450266,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1794304240","clinical_significance":[],"end":140450270,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140450270,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"feature_type":"variation","strand":1,"alleles":["AA","A"],"end":140450275,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450274,"clinical_significance":[],"seq_region_name":"7","id":"rs1226288316"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450275,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140450275,"clinical_significance":[],"seq_region_name":"7","id":"rs1794304279"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450276,"source":"dbSNP","strand":1,"feature_type":"variation","end":140450276,"alleles":["T","G"],"seq_region_name":"7","id":"rs1275070083","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140450277,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450277,"clinical_significance":[],"seq_region_name":"7","id":"rs150808450"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140450278,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450278,"source":"dbSNP","seq_region_name":"7","id":"rs529889982","clinical_significance":[]},{"alleles":["T","C"],"end":140450280,"strand":1,"feature_type":"variation","start":140450280,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs973160039","clinical_significance":[]},{"start":140450282,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140450282,"alleles":["G","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1026596226","clinical_significance":[]},{"seq_region_name":"7","id":"rs1343067589","clinical_significance":[],"start":140450287,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","A"],"end":140450287,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1279525506","clinical_significance":[],"end":140450291,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140450291,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"id":"rs1488551873","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140450294,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450294,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs180709947","end":140450296,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140450296,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs950504251","clinical_significance":[],"strand":1,"feature_type":"variation","end":140450297,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450297,"source":"dbSNP"},{"start":140450298,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140450298,"strand":1,"feature_type":"variation","id":"rs765942461","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450303,"source":"dbSNP","strand":1,"feature_type":"variation","end":140450303,"alleles":["C","T"],"seq_region_name":"7","id":"rs987406173","clinical_significance":[]},{"id":"rs1794304537","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450305,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GTG","G"],"end":140450307},{"seq_region_name":"7","id":"rs1794304551","clinical_significance":[],"alleles":["G","C"],"end":140450307,"strand":1,"feature_type":"variation","start":140450307,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"start":140450310,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140450310,"alleles":["T","A"],"strand":1,"feature_type":"variation","id":"rs1425735985","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs911773455","clinical_significance":[],"alleles":["C","G","T"],"end":140450311,"strand":1,"feature_type":"variation","start":140450311,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"source":"dbSNP","start":140450312,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140450312,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1477028431"},{"start":140450313,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140450313,"alleles":["A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794304602","clinical_significance":[]},{"source":"dbSNP","start":140450318,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140450318,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794304624"},{"clinical_significance":[],"seq_region_name":"7","id":"rs944028037","feature_type":"variation","strand":1,"end":140450319,"alleles":["C","A","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450319},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450320,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140450320,"seq_region_name":"7","id":"rs560555140","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450322,"source":"dbSNP","strand":1,"feature_type":"variation","end":140450322,"alleles":["C","T"],"seq_region_name":"7","id":"rs1794304701","clinical_significance":[]},{"id":"rs921273052","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450325,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140450325},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140450326,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450326,"source":"dbSNP","seq_region_name":"7","id":"rs1794304726","clinical_significance":[]},{"clinical_significance":[],"id":"rs1794304739","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450327,"feature_type":"variation","strand":1,"end":140450327,"alleles":["C","T"]},{"alleles":["C","T"],"end":140450329,"strand":1,"feature_type":"variation","start":140450329,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1284168128","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140450333,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450333,"clinical_significance":[],"seq_region_name":"7","id":"rs1794304772"},{"seq_region_name":"7","id":"rs1794304791","clinical_significance":[],"start":140450337,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140450337,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140450343,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450343,"source":"dbSNP","seq_region_name":"7","id":"rs1215462559","clinical_significance":[]},{"id":"rs369162739","seq_region_name":"7","clinical_significance":[],"start":140450344,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140450344,"alleles":["T","C","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs936779035","clinical_significance":[],"end":140450348,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","start":140450348,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs73485139","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140450349,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450349,"source":"dbSNP"},{"id":"rs184358080","seq_region_name":"7","clinical_significance":[],"start":140450352,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140450352,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"alleles":["ACAA","A"],"end":140450362,"strand":1,"feature_type":"variation","start":140450359,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs202054443","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450360,"feature_type":"variation","strand":1,"end":140450360,"alleles":["C","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1563082936"},{"seq_region_name":"7","id":"rs369616935","clinical_significance":[],"start":140450361,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["AAAAAAA","AAAAAA","AAAAAAAA"],"end":140450367,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1400092837","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450363,"feature_type":"variation","strand":1,"end":140450363,"alleles":["A","T"]},{"alleles":["A","C"],"end":140450366,"feature_type":"variation","strand":1,"source":"dbSNP","start":140450366,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs937659780"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794305059","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450368,"feature_type":"variation","strand":1,"end":140450367,"alleles":["-","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1286787254","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450368,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140450368},{"seq_region_name":"7","id":"rs1794305089","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450371,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140450371},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140450373,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450373,"source":"dbSNP","id":"rs1794305108","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140450374,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450374,"source":"dbSNP","id":"rs1794305122","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1429641407","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450378,"feature_type":"variation","strand":1,"end":140450378,"alleles":["A","G"]},{"start":140450379,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140450379,"alleles":["G","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1359505071","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450384,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140450384,"seq_region_name":"7","id":"rs2130220292","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140450385,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450385,"clinical_significance":[],"seq_region_name":"7","id":"rs914089781"},{"start":140450390,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G","T"],"end":140450390,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1178038751","clinical_significance":[]},{"seq_region_name":"7","id":"rs1412684995","clinical_significance":[],"start":140450392,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140450392,"strand":1,"feature_type":"variation"},{"id":"rs1794305182","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450393,"source":"dbSNP","strand":1,"feature_type":"variation","end":140450393,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1794305202","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["TTTT","TTT"],"end":140450397,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450394,"source":"dbSNP"},{"source":"dbSNP","start":140450395,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140450395,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794305216"},{"feature_type":"variation","strand":1,"end":140450396,"alleles":["T","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450396,"clinical_significance":[],"seq_region_name":"7","id":"rs2130220327"},{"end":140450397,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140450397,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1054884943"},{"seq_region_name":"7","id":"rs1794305263","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450398,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140450398},{"seq_region_name":"7","id":"rs1794305286","clinical_significance":[],"alleles":["T","A"],"end":140450399,"strand":1,"feature_type":"variation","start":140450399,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450403,"feature_type":"variation","strand":1,"end":140450405,"alleles":["CTC","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794305313"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450404,"feature_type":"variation","strand":1,"end":140450404,"alleles":["T","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794305343"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794305378","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450405,"feature_type":"variation","strand":1,"end":140450405,"alleles":["C","T"]},{"end":140450406,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140450406,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1794305406","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs888174195","seq_region_name":"7","end":140450408,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140450408,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1794305460","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450414,"source":"dbSNP","strand":1,"feature_type":"variation","end":140450414,"alleles":["T","C"]},{"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140450418,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450418,"source":"dbSNP","seq_region_name":"7","id":"rs945508575","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794305519","source":"dbSNP","start":140450422,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140450422,"alleles":["T","C"],"feature_type":"variation","strand":1},{"id":"rs1794305542","seq_region_name":"7","clinical_significance":[],"end":140450425,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140450425,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140450431,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450431,"clinical_significance":[],"seq_region_name":"7","id":"rs1794305565"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450433,"source":"dbSNP","strand":1,"feature_type":"variation","end":140450433,"alleles":["T","C"],"seq_region_name":"7","id":"rs1420886024","clinical_significance":[]},{"clinical_significance":[],"id":"rs570999051","seq_region_name":"7","source":"dbSNP","start":140450435,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140450435,"alleles":["C","A"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140450436,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450436,"source":"dbSNP","seq_region_name":"7","id":"rs1005402859","clinical_significance":[]},{"end":140450437,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140450437,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1483733351","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563082952","end":140450439,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140450439,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"end":140450444,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140450444,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1239570498","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450450,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140450450,"seq_region_name":"7","id":"rs769458883","clinical_significance":[]},{"seq_region_name":"7","id":"rs1461212789","clinical_significance":[],"start":140450452,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","C","T"],"end":140450452,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140450453,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140450453,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1046636497"},{"alleles":["T","C"],"end":140450454,"strand":1,"feature_type":"variation","start":140450454,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1218666707","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794305882","clinical_significance":[],"alleles":["AAA","AA"],"end":140450457,"strand":1,"feature_type":"variation","start":140450455,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794305907","alleles":["G","C"],"end":140450458,"feature_type":"variation","strand":1,"source":"dbSNP","start":140450458,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794305920","feature_type":"variation","strand":1,"end":140450459,"alleles":["-","GGAG"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450460},{"alleles":["C","A","T"],"end":140450460,"feature_type":"variation","strand":1,"source":"dbSNP","start":140450460,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794305949"},{"alleles":["T","C"],"end":140450462,"strand":1,"feature_type":"variation","start":140450462,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1794305980","clinical_significance":[]},{"source":"dbSNP","start":140450463,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140450463,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1794306005","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1794306040","clinical_significance":[],"end":140450465,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140450465,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140450471,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450471,"clinical_significance":[],"seq_region_name":"7","id":"rs1794306072"},{"id":"rs896970610","seq_region_name":"7","clinical_significance":[],"alleles":["T","A","C","G"],"end":140450479,"strand":1,"feature_type":"variation","start":140450479,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"start":140450480,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140450480,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794306127","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794306151","clinical_significance":[],"strand":1,"feature_type":"variation","end":140450481,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450481,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450482,"source":"dbSNP","strand":1,"feature_type":"variation","end":140450482,"alleles":["C","G"],"id":"rs1383341266","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450484,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140450484,"clinical_significance":[],"seq_region_name":"7","id":"rs1381996378"},{"end":140450485,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140450485,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs552593802"},{"clinical_significance":[],"seq_region_name":"7","id":"rs75841785","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450487,"feature_type":"variation","strand":1,"end":140450487,"alleles":["C","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1029573432","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140450490,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450490},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450495,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GGGG","G"],"end":140450498,"seq_region_name":"7","id":"rs1794306331","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1372631889","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450498,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140450498},{"alleles":["G","A","T"],"end":140450501,"strand":1,"feature_type":"variation","start":140450501,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs753716402","clinical_significance":[]},{"alleles":["T","TT"],"end":140450502,"feature_type":"variation","strand":1,"source":"dbSNP","start":140450502,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794306427"},{"start":140450503,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","C","G"],"end":140450503,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs954191938","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794306492","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450505,"source":"dbSNP","strand":1,"feature_type":"variation","end":140450505,"alleles":["G","T"]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450511,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","T"],"end":140450511,"seq_region_name":"7","id":"rs773122705","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450512,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140450512,"clinical_significance":[],"id":"rs1794306556","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140450515,"alleles":["A","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450515,"clinical_significance":[],"seq_region_name":"7","id":"rs1055220836"},{"seq_region_name":"7","id":"rs1242316732","clinical_significance":[],"start":140450517,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","AA"],"end":140450517,"strand":1,"feature_type":"variation"},{"end":140450521,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140450521,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1006804366"},{"start":140450522,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140450522,"strand":1,"feature_type":"variation","id":"rs1794306659","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs898820795","alleles":["T","C"],"end":140450526,"feature_type":"variation","strand":1,"source":"dbSNP","start":140450526,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1467163280","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140450528,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450528},{"clinical_significance":[],"seq_region_name":"7","id":"rs189831468","source":"dbSNP","start":140450532,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140450532,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794306752","end":140450535,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140450535,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1585454492","clinical_significance":[],"alleles":["T","G"],"end":140450537,"strand":1,"feature_type":"variation","start":140450537,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"id":"rs1371391029","seq_region_name":"7","source":"dbSNP","start":140450538,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140450538,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140450540,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450540,"source":"dbSNP","id":"rs995010567","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1258884011","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450541,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140450541},{"feature_type":"variation","strand":1,"end":140450543,"alleles":["C","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450543,"clinical_significance":[],"seq_region_name":"7","id":"rs1416247281"},{"seq_region_name":"7","id":"rs1794306918","clinical_significance":[],"alleles":["T","C"],"end":140450545,"strand":1,"feature_type":"variation","start":140450545,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"id":"rs1794306942","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140450547,"strand":1,"feature_type":"variation","start":140450547,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140450555,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450555,"clinical_significance":[],"id":"rs1026048447","seq_region_name":"7"},{"end":140450566,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140450566,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs748880639","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1210146551","alleles":["A","C","T"],"end":140450567,"feature_type":"variation","strand":1,"source":"dbSNP","start":140450567,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140450568,"alleles":["G","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450568,"clinical_significance":[],"id":"rs1268359143","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140450569,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450569,"source":"dbSNP","seq_region_name":"7","id":"rs1239211903","clinical_significance":[]},{"source":"dbSNP","start":140450570,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140450570,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs754736444","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1794307150","clinical_significance":[],"start":140450576,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["TT","TTT"],"end":140450577,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140450578,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450578,"source":"dbSNP","seq_region_name":"7","id":"rs1794307168","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794307195","clinical_significance":[],"strand":1,"feature_type":"variation","end":140450580,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450580,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1794307213","seq_region_name":"7","alleles":["A","G"],"end":140450584,"feature_type":"variation","strand":1,"source":"dbSNP","start":140450584,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs950536381","feature_type":"variation","strand":1,"end":140450585,"alleles":["T","A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450585},{"seq_region_name":"7","id":"rs957422873","clinical_significance":[],"start":140450586,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140450586,"strand":1,"feature_type":"variation"},{"end":140450587,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140450587,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1585454526","clinical_significance":[]},{"seq_region_name":"7","id":"rs1008702776","clinical_significance":[],"strand":1,"feature_type":"variation","end":140450588,"alleles":["G","C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450588,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1794307297","clinical_significance":[],"end":140450592,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140450592,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1563082999","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450593,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140450593},{"clinical_significance":[],"id":"rs1018781902","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450594,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140450594},{"end":140450596,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140450596,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs770718811"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140450597,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450597,"clinical_significance":[],"seq_region_name":"7","id":"rs142800279"},{"clinical_significance":[],"seq_region_name":"7","id":"rs921275906","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140450600,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450600},{"alleles":["C","T"],"end":140450602,"strand":1,"feature_type":"variation","start":140450602,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs181432032","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450604,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140450604,"clinical_significance":[],"seq_region_name":"7","id":"rs1794307481"},{"seq_region_name":"7","id":"rs1321891001","clinical_significance":[],"end":140450605,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140450605,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"source":"dbSNP","start":140450609,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140450609,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794307533"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450610,"feature_type":"variation","strand":1,"end":140450610,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130220644"},{"start":140450612,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140450612,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs913412879","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130220648","source":"dbSNP","start":140450614,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140450614,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs989972885","clinical_significance":[],"alleles":["T","A","C"],"end":140450615,"strand":1,"feature_type":"variation","start":140450615,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"alleles":["T","C"],"end":140450617,"feature_type":"variation","strand":1,"source":"dbSNP","start":140450617,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794310001"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450618,"source":"dbSNP","strand":1,"feature_type":"variation","end":140450618,"alleles":["A","G"],"seq_region_name":"7","id":"rs1794310027","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130220658","clinical_significance":[],"start":140450623,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140450623,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450624,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140450624,"seq_region_name":"7","id":"rs1794310052","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450627,"source":"dbSNP","strand":1,"feature_type":"variation","end":140450627,"alleles":["T","C"],"seq_region_name":"7","id":"rs1794310077","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794310098","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140450628,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450628},{"end":140450630,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140450630,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1381734448","clinical_significance":[]},{"alleles":["G","A"],"end":140450631,"strand":1,"feature_type":"variation","start":140450631,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs982110014","clinical_significance":[]},{"seq_region_name":"7","id":"rs528683280","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450637,"source":"dbSNP","strand":1,"feature_type":"variation","end":140450637,"alleles":["T","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130220679","source":"dbSNP","start":140450638,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140450638,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs186880508","seq_region_name":"7","source":"dbSNP","start":140450641,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140450641,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1794310260","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450647,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140450647},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450652,"feature_type":"variation","strand":1,"end":140450652,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794310282"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450653,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140450653,"seq_region_name":"7","id":"rs1794310307","clinical_significance":[]},{"seq_region_name":"7","id":"rs748107174","clinical_significance":[],"start":140450654,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140450654,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"end":140450655,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140450655,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1297621202","seq_region_name":"7"},{"clinical_significance":[],"id":"rs2130220707","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450656,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140450656},{"clinical_significance":[],"seq_region_name":"7","id":"rs1458493377","end":140450657,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140450657,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140450658,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140450658,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs2130220715","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140450665,"alleles":["AAGTAA","AA"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450660,"clinical_significance":[],"id":"rs1794310427","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1794310456","clinical_significance":[],"end":140450662,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140450662,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs2130220724","clinical_significance":[],"strand":1,"feature_type":"variation","end":140450672,"alleles":["AATAAAATA","AATA"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450664,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794310483","source":"dbSNP","start":140450665,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140450665,"alleles":["A","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1794310509","clinical_significance":[],"alleles":["T","C"],"end":140450666,"strand":1,"feature_type":"variation","start":140450666,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"start":140450668,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140450668,"strand":1,"feature_type":"variation","id":"rs1351792182","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450670,"feature_type":"variation","strand":1,"end":140450670,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794310547"},{"clinical_significance":[],"seq_region_name":"7","id":"rs759146964","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450672,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140450672},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450673,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140450673,"clinical_significance":[],"seq_region_name":"7","id":"rs945453228"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450674,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140450674,"clinical_significance":[],"id":"rs1046586365","seq_region_name":"7"},{"seq_region_name":"7","id":"rs2130220746","clinical_significance":[],"end":140450675,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140450675,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1585454575","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140450679,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450679,"source":"dbSNP"},{"end":140450680,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140450680,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs990456265","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs758276992","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450681,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140450681},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794310776","source":"dbSNP","start":140450683,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","C","G"],"end":140450683,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140450693,"alleles":["TGAGAGTGAG","TGAG"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450684,"source":"dbSNP","seq_region_name":"7","id":"rs1563083024","clinical_significance":[]},{"end":140450685,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140450685,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1438311842"},{"seq_region_name":"7","id":"rs938293197","clinical_significance":[],"alleles":["G","A","C"],"end":140450687,"strand":1,"feature_type":"variation","start":140450687,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"end":140450690,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140450690,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130220778"},{"start":140450694,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140450694,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1563083027","clinical_significance":[]},{"seq_region_name":"7","id":"rs1055355084","clinical_significance":[],"end":140450697,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140450697,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1176079125","source":"dbSNP","start":140450701,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140450723,"alleles":["TAACCACTTCAGATGAACAAGTA","TA"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1794314464","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450707,"source":"dbSNP","strand":1,"feature_type":"variation","end":140450707,"alleles":["C","T"]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450709,"feature_type":"variation","strand":1,"alleles":["TCAGATGAACAAGTATGTTTTTAAAAATTATTTCTCAG","TCAG"],"end":140450746,"clinical_significance":[],"seq_region_name":"7","id":"rs1377073272"},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140450718,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450718,"source":"dbSNP","seq_region_name":"7","id":"rs1794314527","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140450722,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450722,"clinical_significance":[],"seq_region_name":"7","id":"rs898846742"},{"strand":1,"feature_type":"variation","end":140450724,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450724,"source":"dbSNP","seq_region_name":"7","id":"rs535638182","clinical_significance":[]},{"start":140450725,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140450725,"alleles":["G","-"],"strand":1,"feature_type":"variation","id":"rs1392566782","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","A"],"end":140450725,"feature_type":"variation","strand":1,"source":"dbSNP","start":140450725,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794314593"},{"source":"dbSNP","start":140450726,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140450726,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs994476657"},{"feature_type":"variation","strand":1,"end":140450730,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450730,"clinical_significance":[],"id":"rs553972106","seq_region_name":"7"},{"seq_region_name":"7","id":"rs897015294","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450734,"source":"dbSNP","strand":1,"feature_type":"variation","end":140450734,"alleles":["A","C"]},{"seq_region_name":"7","id":"rs1794314735","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450736,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140450736},{"source":"dbSNP","start":140450736,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140450741,"alleles":["TTATTT","TT"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794314768"},{"source":"dbSNP","start":140450739,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140450739,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1794314799","seq_region_name":"7"},{"end":140450740,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140450740,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1794318567","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1242064487","source":"dbSNP","start":140450742,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140450742,"alleles":["C","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1585454626","seq_region_name":"7","feature_type":"variation","strand":1,"end":140450747,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450747},{"clinical_significance":[],"seq_region_name":"7","id":"rs1047519932","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140450748,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450748},{"id":"rs886223825","seq_region_name":"7","clinical_significance":[],"start":140450749,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140450749,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs761312351","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450752,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140450752},{"end":140450753,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140450753,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1387322013"},{"id":"rs572599668","seq_region_name":"7","clinical_significance":[],"alleles":["T","A"],"end":140450761,"strand":1,"feature_type":"variation","start":140450761,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140450764,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450764,"source":"dbSNP","seq_region_name":"7","id":"rs1794320485","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450766,"feature_type":"variation","strand":1,"end":140450767,"alleles":["CC","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1301437961"},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140450767,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450767,"clinical_significance":[],"id":"rs1794320550","seq_region_name":"7"},{"id":"rs1424258557","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140450768,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450768,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1332367030","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450769,"feature_type":"variation","strand":1,"end":140450769,"alleles":["G","A","C"]},{"seq_region_name":"7","id":"rs1794320641","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450773,"source":"dbSNP","strand":1,"feature_type":"variation","end":140450773,"alleles":["T","A"]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450775,"feature_type":"variation","strand":1,"end":140450775,"alleles":["A","C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794320669"},{"end":140450776,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140450776,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1794320690","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","A"],"end":140450778,"strand":1,"feature_type":"variation","start":140450778,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1794320709","clinical_significance":[]},{"id":"rs1018814540","seq_region_name":"7","clinical_significance":[],"start":140450780,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140450780,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140450781,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450781,"clinical_significance":[],"id":"rs1794320747","seq_region_name":"7"},{"end":140450783,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140450783,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1794320762","clinical_significance":[]},{"start":140450784,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140450784,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs964547498","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450785,"source":"dbSNP","strand":1,"feature_type":"variation","end":140450785,"alleles":["G","C"],"id":"rs1160766362","seq_region_name":"7","clinical_significance":[]},{"id":"rs6969623","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450788,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140450788},{"clinical_significance":[],"seq_region_name":"7","id":"rs1458278519","alleles":["G","A"],"end":140450793,"feature_type":"variation","strand":1,"source":"dbSNP","start":140450793,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140450795,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450795,"clinical_significance":[],"seq_region_name":"7","id":"rs1032889083"},{"clinical_significance":[],"id":"rs1270403501","seq_region_name":"7","source":"dbSNP","start":140450801,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140450801,"alleles":["C","G","T"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140450802,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450802,"clinical_significance":[],"id":"rs1178956796","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1263480697","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450803,"source":"dbSNP","strand":1,"feature_type":"variation","end":140450803,"alleles":["G","A"]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450804,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140450804,"seq_region_name":"7","id":"rs1218467679","clinical_significance":[]},{"id":"rs1794321001","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140450808,"alleles":["T","C","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450808,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1348234229","end":140450809,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140450809,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"start":140450810,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","C","T"],"end":140450810,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794321050","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450811,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140450811,"seq_region_name":"7","id":"rs1259977328","clinical_significance":[]},{"seq_region_name":"7","id":"rs1233863649","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140450812,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450812,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1585454672","clinical_significance":[],"start":140450813,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","G"],"end":140450813,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130220921","source":"dbSNP","start":140450817,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140450817,"feature_type":"variation","strand":1},{"alleles":["A","C"],"end":140450818,"feature_type":"variation","strand":1,"source":"dbSNP","start":140450818,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs958287367","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1313948656","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140450821,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450821,"source":"dbSNP"},{"end":140450822,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140450822,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794321158"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794321178","source":"dbSNP","start":140450822,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["GG","GGG"],"end":140450823,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1249073501","source":"dbSNP","start":140450826,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140450826,"alleles":["A","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1418953406","clinical_significance":[],"alleles":["C","T"],"end":140450827,"strand":1,"feature_type":"variation","start":140450827,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794321242","source":"dbSNP","start":140450828,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140450828,"alleles":["C","T"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140450829,"alleles":["A","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450829,"clinical_significance":[],"seq_region_name":"7","id":"rs1404427143"},{"start":140450830,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140450830,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794321280","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450836,"feature_type":"variation","strand":1,"end":140450836,"alleles":["C","A","G","T"],"clinical_significance":[],"id":"rs989471883","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794321327","end":140450837,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140450837,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"end":140450840,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140450840,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794321344"},{"clinical_significance":[],"id":"rs1794321361","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450842,"feature_type":"variation","strand":1,"end":140450842,"alleles":["T","A","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs889684395","source":"dbSNP","start":140450843,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140450843,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1794321412","clinical_significance":[],"end":140450845,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140450845,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"id":"rs1380787718","seq_region_name":"7","clinical_significance":[],"start":140450846,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140450846,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1794321447","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450849,"feature_type":"variation","strand":1,"end":140450849,"alleles":["A","T"]},{"source":"dbSNP","start":140450853,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140450853,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs558631070"},{"seq_region_name":"7","id":"rs1020906671","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450861,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140450861},{"seq_region_name":"7","id":"rs1188825437","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140450866,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450866,"source":"dbSNP"},{"end":140450877,"alleles":["AAAAAAA","AAAAAA","AAAAAAAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140450871,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1006856674"},{"seq_region_name":"7","id":"rs1467966740","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450872,"source":"dbSNP","strand":1,"feature_type":"variation","end":140450872,"alleles":["A","G"]},{"clinical_significance":[],"id":"rs1794321581","seq_region_name":"7","source":"dbSNP","start":140450878,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140450878,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1427827956","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450882,"feature_type":"variation","strand":1,"end":140450882,"alleles":["C","A","G"]},{"id":"rs1794321614","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140450883,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450883,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1563083059","clinical_significance":[],"strand":1,"feature_type":"variation","end":140450887,"alleles":["C","CC"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450887,"source":"dbSNP"},{"clinical_significance":[],"id":"rs966788375","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450888,"feature_type":"variation","strand":1,"end":140450888,"alleles":["A","G","T"]},{"clinical_significance":[],"id":"rs1194847273","seq_region_name":"7","feature_type":"variation","strand":1,"end":140450889,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450889},{"end":140450891,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140450891,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1444980993"},{"clinical_significance":[],"id":"rs1794321703","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450892,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140450892},{"id":"rs1260772432","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140450897,"strand":1,"feature_type":"variation","start":140450897,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"alleles":["T","C"],"end":140450902,"feature_type":"variation","strand":1,"source":"dbSNP","start":140450902,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1585454717","seq_region_name":"7"},{"alleles":["T","C"],"end":140450905,"feature_type":"variation","strand":1,"source":"dbSNP","start":140450905,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1420560826"},{"clinical_significance":[],"id":"rs1794321788","seq_region_name":"7","end":140450906,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140450906,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"start":140450911,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140450915,"alleles":["AGCTA","AGCTAGCTA"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794321811","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs576716852","source":"dbSNP","start":140450913,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140450913,"feature_type":"variation","strand":1},{"start":140450914,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140450914,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs928151398","clinical_significance":[]},{"start":140450917,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140450917,"strand":1,"feature_type":"variation","id":"rs1261203439","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794321871","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450920,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140450920},{"strand":1,"feature_type":"variation","end":140450921,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450921,"source":"dbSNP","seq_region_name":"7","id":"rs796607696","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140450924,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450924,"source":"dbSNP","seq_region_name":"7","id":"rs938170928","clinical_significance":[]},{"seq_region_name":"7","id":"rs1010315839","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450929,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140450929},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140450930,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450930,"clinical_significance":[],"id":"rs1225503045","seq_region_name":"7"},{"id":"rs1585454741","seq_region_name":"7","clinical_significance":[],"alleles":["C","G"],"end":140450931,"strand":1,"feature_type":"variation","start":140450931,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1163779476","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450934,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140450934},{"clinical_significance":[],"seq_region_name":"7","id":"rs1400489181","source":"dbSNP","start":140450936,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140450936,"alleles":["G","A","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1794322057","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450941,"source":"dbSNP","strand":1,"feature_type":"variation","end":140450941,"alleles":["A","G"]},{"id":"rs1794322068","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450942,"source":"dbSNP","strand":1,"feature_type":"variation","end":140450942,"alleles":["C","T"]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450943,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140450943,"id":"rs991483599","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140450947,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140450947,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs920824763"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794322115","source":"dbSNP","start":140450950,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140450950,"feature_type":"variation","strand":1},{"alleles":["G","A"],"end":140450951,"feature_type":"variation","strand":1,"source":"dbSNP","start":140450951,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs112123913","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs971976618","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450952,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140450952},{"start":140450954,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140450954,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794322169","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450959,"source":"dbSNP","strand":1,"feature_type":"variation","end":140450959,"alleles":["G","A"],"seq_region_name":"7","id":"rs1794322191","clinical_significance":[]},{"clinical_significance":[],"id":"rs1047469838","seq_region_name":"7","source":"dbSNP","start":140450963,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140450963,"alleles":["T","A","C","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs562609361","clinical_significance":[],"strand":1,"feature_type":"variation","end":140450965,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450965,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1396575397","clinical_significance":[],"end":140450969,"alleles":["T","C","G"],"strand":1,"feature_type":"variation","start":140450969,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1295045208","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450970,"feature_type":"variation","strand":1,"end":140450970,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794322304","end":140450971,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140450971,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140450972,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140450972,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794322330"},{"strand":1,"feature_type":"variation","end":140450973,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450973,"source":"dbSNP","seq_region_name":"7","id":"rs1372159000","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1474184746","feature_type":"variation","strand":1,"end":140450974,"alleles":["CC","CCC"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450973},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450977,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140450977,"clinical_significance":[],"seq_region_name":"7","id":"rs1187942113"},{"start":140450980,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140450980,"alleles":["C","A","G","T"],"strand":1,"feature_type":"variation","id":"rs1353389368","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140450981,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450981,"clinical_significance":[],"seq_region_name":"7","id":"rs886089376"},{"id":"rs944450347","seq_region_name":"7","clinical_significance":[],"start":140450982,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140450982,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs757424263","alleles":["G","A"],"end":140450983,"feature_type":"variation","strand":1,"source":"dbSNP","start":140450983,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794322550","feature_type":"variation","strand":1,"end":140450985,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450985},{"strand":1,"feature_type":"variation","end":140451012,"alleles":["CACTGCACTCCAGCCTGTTGACAGAGCA","CA"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450985,"source":"dbSNP","seq_region_name":"7","id":"rs1794322570","clinical_significance":[]},{"seq_region_name":"7","id":"rs1206741310","clinical_significance":[],"strand":1,"feature_type":"variation","end":140450986,"alleles":["A","C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450986,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1338924443","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450987,"feature_type":"variation","strand":1,"end":140450987,"alleles":["C","G","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1247307470","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450991,"feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140450991},{"clinical_significance":[],"id":"rs1794323821","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140450992,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140450992},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794323835","source":"dbSNP","start":140450993,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140451022,"alleles":["TCCAGCCTGTTGACAGAGCAAGACTCCGTC","TC"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140450995,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140450995,"source":"dbSNP","id":"rs981610824","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1448161708","clinical_significance":[],"start":140450996,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","T"],"end":140450996,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1314861620","clinical_significance":[],"start":140450997,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","GG"],"end":140450997,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1403093425","clinical_significance":[],"alleles":["T","-"],"end":140451000,"strand":1,"feature_type":"variation","start":140451000,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140451003,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451003,"clinical_significance":[],"seq_region_name":"7","id":"rs2130221226"},{"id":"rs1794323979","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451004,"source":"dbSNP","strand":1,"feature_type":"variation","end":140451004,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1330246041","source":"dbSNP","start":140451008,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140451008,"alleles":["G","C"],"feature_type":"variation","strand":1},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451009,"feature_type":"variation","strand":1,"end":140451009,"alleles":["A","G"],"clinical_significance":[],"id":"rs1249739059","seq_region_name":"7"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451011,"feature_type":"variation","strand":1,"alleles":["C","A","G"],"end":140451011,"clinical_significance":[],"id":"rs745935263","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794324122","alleles":["A","G"],"end":140451013,"feature_type":"variation","strand":1,"source":"dbSNP","start":140451013,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140451017,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451017,"clinical_significance":[],"id":"rs1183013613","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794324177","source":"dbSNP","start":140451018,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140451019,"alleles":["CC","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs531379745","feature_type":"variation","strand":1,"alleles":["-","A"],"end":140451018,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451019},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451019,"feature_type":"variation","strand":1,"end":140451019,"alleles":["C","A","G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs199846523"},{"id":"rs1234549591","seq_region_name":"7","clinical_significance":[],"end":140451020,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140451020,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"source":"dbSNP","start":140451021,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140451021,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1179696765"},{"id":"rs1437280405","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140451025,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451025,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs909590660","end":140451035,"alleles":["AAAAAAAAAA","AAAAAAAAA","AAAAAAAAAAA","AAAAAAAAAAAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140451026,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451027,"feature_type":"variation","strand":1,"end":140451027,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs995989604"},{"seq_region_name":"7","id":"rs1794324522","clinical_significance":[],"strand":1,"feature_type":"variation","end":140451031,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451031,"source":"dbSNP"},{"alleles":["AAAACAAAACA","AAAACA"],"end":140451042,"feature_type":"variation","strand":1,"source":"dbSNP","start":140451032,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1794324549","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140451034,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451034,"clinical_significance":[],"seq_region_name":"7","id":"rs2130221325"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1291410866","end":140451035,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140451035,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"start":140451036,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140451036,"alleles":["C","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1241345160","clinical_significance":[]},{"start":140451040,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["ACACA","ACA"],"end":140451044,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794324682","clinical_significance":[]},{"source":"dbSNP","start":140451043,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140451043,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1376105870","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs941000079","source":"dbSNP","start":140451049,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140451056,"alleles":["AAAAAAAA","AAAAAAA","AAAAAAAAA"],"feature_type":"variation","strand":1},{"end":140451050,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140451050,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794324819"},{"source":"dbSNP","start":140451054,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140451054,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs188966791"},{"id":"rs893090312","seq_region_name":"7","clinical_significance":[],"start":140451056,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140451056,"alleles":["A","C","G"],"strand":1,"feature_type":"variation"},{"start":140451057,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140451057,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794324964","clinical_significance":[]},{"start":140451059,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140451059,"alleles":["A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794324998","clinical_significance":[]},{"id":"rs972904192","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451060,"source":"dbSNP","strand":1,"feature_type":"variation","end":140451060,"alleles":["T","G"]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451064,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140451064,"seq_region_name":"7","id":"rs1794325099","clinical_significance":[]},{"alleles":["C","T"],"end":140451065,"strand":1,"feature_type":"variation","start":140451065,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs2130221397","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451066,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140451066,"clinical_significance":[],"seq_region_name":"7","id":"rs560427368"},{"clinical_significance":[],"id":"rs933835212","seq_region_name":"7","feature_type":"variation","strand":1,"end":140451073,"alleles":["TTTT","TTTTT"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451070},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794325264","feature_type":"variation","strand":1,"end":140451071,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451071},{"alleles":["C","A","T"],"end":140451074,"strand":1,"feature_type":"variation","start":140451074,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1162637812","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130221442","clinical_significance":[],"strand":1,"feature_type":"variation","end":140451075,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451075,"source":"dbSNP"},{"seq_region_name":"7","id":"rs749708444","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140451079,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451079,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1409938505","source":"dbSNP","start":140451080,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["AAAA","AAA"],"end":140451083,"feature_type":"variation","strand":1},{"id":"rs1020939144","seq_region_name":"7","clinical_significance":[],"start":140451085,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140451085,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140451087,"alleles":["C","A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451087,"source":"dbSNP","id":"rs1156719277","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1469615293","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451097,"source":"dbSNP","strand":1,"feature_type":"variation","end":140451097,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs1794325498","clinical_significance":[],"strand":1,"feature_type":"variation","end":140451098,"alleles":["AA","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451097,"source":"dbSNP"},{"start":140451101,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["TTT","TT"],"end":140451103,"strand":1,"feature_type":"variation","id":"rs2130221478","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs765477598","clinical_significance":[],"end":140451104,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140451104,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"end":140451105,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140451105,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1201690085"},{"alleles":["G","A"],"end":140451107,"strand":1,"feature_type":"variation","start":140451107,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1489904549","clinical_significance":[]},{"alleles":["G","C"],"end":140451112,"feature_type":"variation","strand":1,"source":"dbSNP","start":140451112,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794325613"},{"seq_region_name":"7","id":"rs143703002","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451114,"source":"dbSNP","strand":1,"feature_type":"variation","end":140451114,"alleles":["C","A","G","T"]},{"end":140451115,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140451115,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1794325698","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451116,"feature_type":"variation","strand":1,"end":140451127,"alleles":["GGCTGTTTGGCT","GGCT"],"clinical_significance":[],"id":"rs1794325726","seq_region_name":"7"},{"end":140451118,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140451118,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1035073642"},{"clinical_significance":[],"id":"rs1794325754","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140451120,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451120},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794325782","source":"dbSNP","start":140451126,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140451126,"alleles":["C","T"],"feature_type":"variation","strand":1},{"id":"rs181654024","seq_region_name":"7","clinical_significance":[],"end":140451134,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140451134,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1367354975","end":140451137,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140451137,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140451141,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140451144,"alleles":["CCCC","CCCCC"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585454923"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451145,"source":"dbSNP","strand":1,"feature_type":"variation","end":140451145,"alleles":["A","C"],"seq_region_name":"7","id":"rs1585454924","clinical_significance":[]},{"seq_region_name":"7","id":"rs959817108","clinical_significance":[],"start":140451148,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","T"],"end":140451148,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451149,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140451149,"seq_region_name":"7","id":"rs1314658088","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140451150,"alleles":["T","C","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451150,"clinical_significance":[],"id":"rs1585454931","seq_region_name":"7"},{"id":"rs991038118","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140451153,"alleles":["A","G","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451153,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585454941","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140451154,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451154},{"id":"rs1794326047","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140451155,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451155,"source":"dbSNP"},{"start":140451156,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","T"],"end":140451156,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794326077","clinical_significance":[]},{"id":"rs1585454945","seq_region_name":"7","clinical_significance":[],"alleles":["T","C","G"],"end":140451158,"strand":1,"feature_type":"variation","start":140451158,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"start":140451160,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140451160,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794326122","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451163,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140451163,"clinical_significance":[],"seq_region_name":"7","id":"rs1794326148"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451164,"source":"dbSNP","strand":1,"feature_type":"variation","end":140451164,"alleles":["A","G"],"seq_region_name":"7","id":"rs1231959698","clinical_significance":[]},{"end":140451165,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140451165,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1282660775","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794326234","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451169,"source":"dbSNP","strand":1,"feature_type":"variation","end":140451169,"alleles":["C","T"]},{"feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140451174,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451174,"clinical_significance":[],"seq_region_name":"7","id":"rs942644686"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794326303","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451175,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140451175},{"clinical_significance":[],"id":"rs1346416206","seq_region_name":"7","feature_type":"variation","strand":1,"end":140451180,"alleles":["A","C","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451180},{"start":140451194,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140451205,"alleles":["TGTACCAGCATG","TG"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1283299717","clinical_significance":[]},{"source":"dbSNP","start":140451195,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140451195,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1563083135"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1406263448","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451196,"feature_type":"variation","strand":1,"alleles":["TACC","TACCTACC"],"end":140451199},{"clinical_significance":[],"seq_region_name":"7","id":"rs1343208462","source":"dbSNP","start":140451197,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140451197,"alleles":["A","G"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140451198,"alleles":["C","G","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451198,"clinical_significance":[],"seq_region_name":"7","id":"rs920759186"},{"feature_type":"variation","strand":1,"end":140451199,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451199,"clinical_significance":[],"seq_region_name":"7","id":"rs1794326505"},{"clinical_significance":[],"seq_region_name":"7","id":"rs930907159","source":"dbSNP","start":140451200,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140451200,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140451204,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451204,"source":"dbSNP","seq_region_name":"7","id":"rs893172435","clinical_significance":[]},{"alleles":["GG","G"],"end":140451206,"strand":1,"feature_type":"variation","start":140451205,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1316040565","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794326643","clinical_significance":[],"alleles":["G","A"],"end":140451208,"strand":1,"feature_type":"variation","start":140451208,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1413973593","clinical_significance":[],"start":140451210,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140451210,"strand":1,"feature_type":"variation"},{"alleles":["C","G"],"end":140451212,"feature_type":"variation","strand":1,"source":"dbSNP","start":140451212,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1278550057"},{"seq_region_name":"7","id":"rs1425801241","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451214,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140451214},{"seq_region_name":"7","id":"rs1020807549","clinical_significance":[],"start":140451216,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140451216,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"start":140451219,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A","C","T"],"end":140451219,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs769171101","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140451220,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451220,"clinical_significance":[],"seq_region_name":"7","id":"rs1794326813"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794326843","source":"dbSNP","start":140451222,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140451222,"alleles":["G","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1003357131","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140451224,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451224},{"seq_region_name":"7","id":"rs1794326910","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140451228,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451228,"source":"dbSNP"},{"source":"dbSNP","start":140451231,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140451231,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs983692393","seq_region_name":"7"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451233,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140451233,"clinical_significance":[],"seq_region_name":"7","id":"rs1034550255"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794326999","source":"dbSNP","start":140451234,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140451234,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140451245,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140451245,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794327020"},{"source":"dbSNP","start":140451246,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140451246,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1240718082"},{"start":140451251,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140451251,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs1794327069","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451254,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140451254,"id":"rs1794327098","seq_region_name":"7","clinical_significance":[]},{"id":"rs907557780","seq_region_name":"7","clinical_significance":[],"end":140451255,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140451255,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"id":"rs1794327151","seq_region_name":"7","alleles":["G","A"],"end":140451260,"feature_type":"variation","strand":1,"source":"dbSNP","start":140451260,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"start":140451262,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140451262,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs958860541","clinical_significance":[]},{"source":"dbSNP","start":140451265,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140451265,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794327212"},{"seq_region_name":"7","id":"rs564623794","clinical_significance":[],"alleles":["C","A","T"],"end":140451268,"strand":1,"feature_type":"variation","start":140451268,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"start":140451269,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A","T"],"end":140451269,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs145793532","clinical_significance":[]},{"alleles":["T","C"],"end":140451272,"strand":1,"feature_type":"variation","start":140451272,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1222263546","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794327368","clinical_significance":[],"start":140451276,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140451276,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1320766383","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451279,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140451279},{"end":140451280,"alleles":["-","TCATCTGGCAATG"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140451281,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794327424"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1282150374","source":"dbSNP","start":140451281,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140451283,"alleles":["AAA","AAAA"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140451282,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140451282,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794327493"},{"seq_region_name":"7","id":"rs1214791586","clinical_significance":[],"start":140451284,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140451284,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"end":140451285,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140451285,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1307008513"},{"alleles":["T","C"],"end":140451287,"strand":1,"feature_type":"variation","start":140451287,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1268137266","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140451288,"alleles":["C","A","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451288,"clinical_significance":[],"seq_region_name":"7","id":"rs186311425"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794327732","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451291,"feature_type":"variation","strand":1,"end":140451291,"alleles":["C","G"]},{"source":"dbSNP","start":140451295,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140451295,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs2130222021","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1794327764","clinical_significance":[],"start":140451300,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140451300,"strand":1,"feature_type":"variation"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451301,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140451301,"clinical_significance":[],"seq_region_name":"7","id":"rs1283125061"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451303,"source":"dbSNP","strand":1,"feature_type":"variation","end":140451303,"alleles":["C","A"],"seq_region_name":"7","id":"rs758446989","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794327885","clinical_significance":[],"strand":1,"feature_type":"variation","end":140451307,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451307,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1794327921","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451309,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140451309},{"end":140451310,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140451310,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs900283942","clinical_significance":[]},{"alleles":["A","C","G"],"end":140451316,"feature_type":"variation","strand":1,"source":"dbSNP","start":140451316,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1484951450"},{"end":140451322,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140451322,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1405426050","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs191054378","source":"dbSNP","start":140451323,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140451323,"alleles":["G","A","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1243098787","feature_type":"variation","strand":1,"end":140451325,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451325},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140451327,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451327,"clinical_significance":[],"seq_region_name":"7","id":"rs1417658661"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130222123","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140451330,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451330},{"seq_region_name":"7","id":"rs1794328199","clinical_significance":[],"alleles":["C","T"],"end":140451332,"strand":1,"feature_type":"variation","start":140451332,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs972401353","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451337,"feature_type":"variation","strand":1,"end":140451337,"alleles":["C","G","T"]},{"seq_region_name":"7","id":"rs2130222151","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451345,"source":"dbSNP","strand":1,"feature_type":"variation","end":140451345,"alleles":["T","C"]},{"source":"dbSNP","start":140451347,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140451347,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794328261"},{"seq_region_name":"7","id":"rs1585455081","clinical_significance":[],"alleles":["A","G"],"end":140451352,"strand":1,"feature_type":"variation","start":140451352,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"id":"rs1054317405","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451353,"feature_type":"variation","strand":1,"end":140451353,"alleles":["C","T"]},{"id":"rs536272405","seq_region_name":"7","clinical_significance":[],"end":140451354,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140451354,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1010121574","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451357,"source":"dbSNP","strand":1,"feature_type":"variation","end":140451357,"alleles":["G","A","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1261894226","end":140451358,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140451358,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140451361,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451361,"source":"dbSNP","seq_region_name":"7","id":"rs1585455099","clinical_significance":[]},{"start":140451363,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140451363,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585455102","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs116051418","source":"dbSNP","start":140451371,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140451371,"feature_type":"variation","strand":1},{"start":140451382,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140451382,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1308844330","clinical_significance":[]},{"end":140451384,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140451384,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1293037359"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794328754","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451389,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140451389},{"strand":1,"feature_type":"variation","end":140451394,"alleles":["TAT","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451392,"source":"dbSNP","seq_region_name":"7","id":"rs1794328812","clinical_significance":[]},{"start":140451394,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140451394,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs547575989","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140451396,"alleles":["A","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451396,"clinical_significance":[],"seq_region_name":"7","id":"rs1213669933"},{"id":"rs1174928802","seq_region_name":"7","clinical_significance":[],"start":140451397,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140451397,"alleles":["C","A","G"],"strand":1,"feature_type":"variation"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451400,"feature_type":"variation","strand":1,"end":140451400,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794328996"},{"end":140451403,"alleles":["AT","ATAT"],"strand":1,"feature_type":"variation","start":140451402,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1794329028","clinical_significance":[]},{"clinical_significance":[],"id":"rs942528177","seq_region_name":"7","source":"dbSNP","start":140451408,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140451408,"alleles":["A","G"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451410,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140451410,"seq_region_name":"7","id":"rs1450354721","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140451413,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451413,"source":"dbSNP","seq_region_name":"7","id":"rs565895398","clinical_significance":[]},{"clinical_significance":[],"id":"rs1585455127","seq_region_name":"7","end":140451414,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140451414,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"id":"rs914466934","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451415,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","G"],"end":140451415},{"alleles":["T","A"],"end":140451417,"feature_type":"variation","strand":1,"source":"dbSNP","start":140451417,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794331650"},{"seq_region_name":"7","id":"rs1794331686","clinical_significance":[],"strand":1,"feature_type":"variation","end":140451419,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451419,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130222335","feature_type":"variation","strand":1,"alleles":["TATCAATATCAA","TATCAATATCAATATCAA"],"end":140451430,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451419},{"end":140451429,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140451429,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1794331720","clinical_significance":[]},{"clinical_significance":[],"id":"rs2130222356","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451433,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140451433},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794331748","end":140451436,"alleles":["CTCT","CT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140451433,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140451436,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451436,"source":"dbSNP","seq_region_name":"7","id":"rs2130222372","clinical_significance":[]},{"id":"rs1298696069","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451444,"source":"dbSNP","strand":1,"feature_type":"variation","end":140451444,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1169979073","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451450,"source":"dbSNP","strand":1,"feature_type":"variation","end":140451450,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1425596567","feature_type":"variation","strand":1,"end":140451451,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451451},{"end":140451457,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140451457,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794331844"},{"end":140451464,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140451464,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs2130222406","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451466,"source":"dbSNP","strand":1,"feature_type":"variation","end":140451466,"alleles":["A","G"],"seq_region_name":"7","id":"rs1794331872","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs373319955","source":"dbSNP","start":140451467,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140451467,"alleles":["T","C"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451472,"source":"dbSNP","strand":1,"feature_type":"variation","end":140451472,"alleles":["A","T"],"id":"rs1182136997","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130222441","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451474,"source":"dbSNP","strand":1,"feature_type":"variation","end":140451474,"alleles":["C","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130222445","feature_type":"variation","strand":1,"end":140451476,"alleles":["C","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451476},{"source":"dbSNP","start":140451477,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140451477,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130222456"},{"seq_region_name":"7","id":"rs1003467250","clinical_significance":[],"start":140451481,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","A","G"],"end":140451481,"strand":1,"feature_type":"variation"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451484,"feature_type":"variation","strand":1,"alleles":["CCCCC","CCCC","CCCCCC"],"end":140451488,"clinical_significance":[],"seq_region_name":"7","id":"rs1428316191"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563083205","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451490,"feature_type":"variation","strand":1,"end":140451490,"alleles":["A","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs78799487","source":"dbSNP","start":140451493,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140451493,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563083209","alleles":["C","T"],"end":140451495,"feature_type":"variation","strand":1,"source":"dbSNP","start":140451495,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs762421413","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451496,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140451496},{"feature_type":"variation","strand":1,"alleles":["ATGATG","ATG"],"end":140451505,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451500,"clinical_significance":[],"id":"rs1361481499","seq_region_name":"7"},{"id":"rs1235151322","seq_region_name":"7","clinical_significance":[],"start":140451505,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140451505,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs907180365","seq_region_name":"7","feature_type":"variation","strand":1,"end":140451506,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451506},{"source":"dbSNP","start":140451514,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140451514,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1657075524"},{"id":"rs1359796105","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451518,"source":"dbSNP","strand":1,"feature_type":"variation","end":140451518,"alleles":["T","C"]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451520,"feature_type":"variation","strand":1,"end":140451520,"alleles":["G","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1003000559"},{"id":"rs1243522689","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140451521,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451521,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140451522,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451522,"clinical_significance":[],"seq_region_name":"7","id":"rs1794332330"},{"source":"dbSNP","start":140451525,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140451525,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794332351"},{"seq_region_name":"7","id":"rs2130222595","clinical_significance":[],"alleles":["A","G"],"end":140451526,"strand":1,"feature_type":"variation","start":140451526,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1358588628","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140451529,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451529,"source":"dbSNP"},{"alleles":["G","A"],"end":140451533,"strand":1,"feature_type":"variation","start":140451533,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1307575121","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451535,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140451535,"id":"rs1393095097","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585455204","source":"dbSNP","start":140451536,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140451536,"alleles":["A","G"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140451538,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140451538,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794332451"},{"seq_region_name":"7","id":"rs1585455208","clinical_significance":[],"end":140451540,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140451540,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1371206236","clinical_significance":[],"strand":1,"feature_type":"variation","end":140451541,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451541,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451542,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140451542,"seq_region_name":"7","id":"rs1794332528","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1035427150","feature_type":"variation","strand":1,"alleles":["T","A"],"end":140451543,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451543},{"end":140451544,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140451544,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1297688041","clinical_significance":[]},{"start":140451547,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140451547,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs959523807","clinical_significance":[]},{"seq_region_name":"7","id":"rs1367754675","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C","T"],"end":140451558,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451558,"source":"dbSNP"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451560,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140451560,"clinical_significance":[],"seq_region_name":"7","id":"rs558342939"},{"alleles":["A","G"],"end":140451563,"feature_type":"variation","strand":1,"source":"dbSNP","start":140451563,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1305786453"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1162032396","source":"dbSNP","start":140451567,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140451567,"alleles":["A","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1794332769","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"TF_binding_site_variant","start":140451567,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AGAAG","AG"],"end":140451571},{"seq_region_name":"7","id":"rs1424472178","clinical_significance":[],"end":140451569,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140451569,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"id":"rs1364769484","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451570,"source":"dbSNP","strand":1,"feature_type":"variation","end":140451570,"alleles":["A","C","T"]},{"consequence_type":"TF_binding_site_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451571,"feature_type":"variation","strand":1,"end":140451571,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs894656700"},{"source":"dbSNP","start":140451572,"consequence_type":"TF_binding_site_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140451572,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1012727883"},{"seq_region_name":"7","id":"rs1585455248","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"TF_binding_site_variant","start":140451573,"source":"dbSNP","strand":1,"feature_type":"variation","end":140451573,"alleles":["T","G"]},{"clinical_significance":[],"id":"rs570545568","seq_region_name":"7","consequence_type":"TF_binding_site_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451574,"feature_type":"variation","strand":1,"end":140451574,"alleles":["G","A"]},{"start":140451576,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"TF_binding_site_variant","end":140451576,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs1027852895","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"TF_binding_site_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451577,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140451577,"clinical_significance":[],"id":"rs1794333079","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1247720918","clinical_significance":[],"end":140451585,"alleles":["ACGTTCCAC","AC"],"strand":1,"feature_type":"variation","start":140451577,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"TF_binding_site_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs554555171","feature_type":"variation","strand":1,"end":140451578,"alleles":["C","G","T"],"consequence_type":"TF_binding_site_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451578},{"assembly_name":"GRCh38","consequence_type":"TF_binding_site_variant","start":140451579,"source":"dbSNP","strand":1,"feature_type":"variation","end":140451579,"alleles":["G","A","T"],"seq_region_name":"7","id":"rs952163452","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794333277","alleles":["A","G"],"end":140451584,"feature_type":"variation","strand":1,"source":"dbSNP","start":140451584,"consequence_type":"TF_binding_site_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140451585,"consequence_type":"TF_binding_site_variant","assembly_name":"GRCh38","end":140451585,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794333315"},{"strand":1,"feature_type":"variation","end":140451587,"alleles":["CCC","CC"],"assembly_name":"GRCh38","consequence_type":"TF_binding_site_variant","start":140451585,"source":"dbSNP","seq_region_name":"7","id":"rs1794333354","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451587,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140451587,"clinical_significance":[],"seq_region_name":"7","id":"rs537429034"},{"seq_region_name":"7","id":"rs1563083244","clinical_significance":[],"start":140451588,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140451588,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1585455281","clinical_significance":[],"start":140451591,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","C"],"end":140451591,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs908090126","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"TF_binding_site_variant","start":140451593,"source":"dbSNP","strand":1,"feature_type":"variation","end":140451593,"alleles":["T","C"]},{"id":"rs1369494390","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140451595,"assembly_name":"GRCh38","consequence_type":"TF_binding_site_variant","start":140451595,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs75317241","consequence_type":"TF_binding_site_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451597,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140451597},{"start":140451599,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"TF_binding_site_variant","end":140451599,"alleles":["C","A"],"strand":1,"feature_type":"variation","id":"rs1358407097","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451609,"source":"dbSNP","strand":1,"feature_type":"variation","end":140451609,"alleles":["T","C"],"id":"rs569774236","seq_region_name":"7","clinical_significance":[]},{"id":"rs1449108072","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140451610,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451610,"source":"dbSNP"},{"source":"dbSNP","start":140451611,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140451611,"alleles":["T","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794334460"},{"start":140451612,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140451612,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1214005782","clinical_significance":[]},{"alleles":["T","C"],"end":140451613,"strand":1,"feature_type":"variation","start":140451613,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1794334522","clinical_significance":[]},{"alleles":["G","C"],"end":140451615,"feature_type":"variation","strand":1,"source":"dbSNP","start":140451615,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1241017822","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1241186681","seq_region_name":"7","source":"dbSNP","start":140451617,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["AA","A","AATTAACACTTAATTAACACTGTTAATTGCAATTAA"],"end":140451618,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1794336529","clinical_significance":[],"start":140451619,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140451619,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140451620,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140451620,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1794336565","seq_region_name":"7"},{"seq_region_name":"7","id":"rs10266321","clinical_significance":[],"alleles":["G","A","C"],"end":140451621,"strand":1,"feature_type":"variation","start":140451621,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"start":140451624,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140451624,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs10224992","clinical_significance":[]},{"clinical_significance":[],"id":"rs1794336850","seq_region_name":"7","source":"dbSNP","start":140451625,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140451625,"alleles":["A","G"],"feature_type":"variation","strand":1},{"start":140451626,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140451627,"alleles":["TT","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794336902","clinical_significance":[]},{"clinical_significance":[],"id":"rs931777028","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451627,"feature_type":"variation","strand":1,"end":140451627,"alleles":["T","G"]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451628,"source":"dbSNP","strand":1,"feature_type":"variation","end":140451628,"alleles":["A","T"],"seq_region_name":"7","id":"rs1347587035","clinical_significance":[]},{"start":140451630,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140451630,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794337038","clinical_significance":[]},{"seq_region_name":"7","id":"rs1301482467","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451631,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140451631},{"seq_region_name":"7","id":"rs955211865","clinical_significance":[],"start":140451632,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140451632,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1794337169","clinical_significance":[],"end":140451635,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140451635,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"feature_type":"variation","strand":1,"end":140451637,"alleles":["G","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451637,"clinical_significance":[],"id":"rs1386057038","seq_region_name":"7"},{"alleles":["A","T"],"end":140451639,"feature_type":"variation","strand":1,"source":"dbSNP","start":140451639,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs554107649","seq_region_name":"7"},{"id":"rs1291003702","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140451640,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451640,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1794337329","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451640,"source":"dbSNP","strand":1,"feature_type":"variation","end":140451646,"alleles":["AAGAAGA","AAGA"]},{"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140451642,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451642,"clinical_significance":[],"seq_region_name":"7","id":"rs182852684"},{"feature_type":"variation","strand":1,"end":140451658,"alleles":["CTCGCTCTC","CTC"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451650,"clinical_significance":[],"seq_region_name":"7","id":"rs1363781810"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1157740929","source":"dbSNP","start":140451652,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140451652,"feature_type":"variation","strand":1},{"end":140451653,"alleles":["G","A","C","T"],"strand":1,"feature_type":"variation","start":140451653,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1480499367","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140451654,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451654,"clinical_significance":[],"seq_region_name":"7","id":"rs1794337584"},{"source":"dbSNP","start":140451660,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140451660,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1794337619","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1794337659","clinical_significance":[],"start":140451661,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140451661,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140451669,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451669,"source":"dbSNP","seq_region_name":"7","id":"rs10231547","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["TT","TTT"],"end":140451670,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451669,"source":"dbSNP","seq_region_name":"7","id":"rs760082808","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140451670,"alleles":["T","C","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451670,"clinical_significance":[],"id":"rs1563083287","seq_region_name":"7"},{"alleles":["A","-"],"end":140451672,"strand":1,"feature_type":"variation","start":140451672,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1585455398","clinical_significance":[]},{"id":"rs914431217","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140451674,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451674,"source":"dbSNP"},{"alleles":["A","T"],"end":140451687,"feature_type":"variation","strand":1,"source":"dbSNP","start":140451687,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130223080"},{"id":"rs1794338058","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451689,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TACA","TACATACA"],"end":140451692},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451690,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140451690,"clinical_significance":[],"seq_region_name":"7","id":"rs1450693111"},{"end":140451692,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140451692,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1262166104"},{"seq_region_name":"7","id":"rs945845674","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451695,"source":"dbSNP","strand":1,"feature_type":"variation","end":140451695,"alleles":["C","A"]},{"end":140451700,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140451700,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1453262236"},{"id":"rs1159197348","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451701,"source":"dbSNP","strand":1,"feature_type":"variation","end":140451701,"alleles":["G","A"]},{"feature_type":"variation","strand":1,"end":140451703,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451703,"clinical_significance":[],"id":"rs1794338313","seq_region_name":"7"},{"alleles":["T","G"],"end":140451708,"feature_type":"variation","strand":1,"source":"dbSNP","start":140451708,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1409988693"},{"seq_region_name":"7","id":"rs1398768925","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451709,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140451709},{"seq_region_name":"7","id":"rs1794338440","clinical_significance":[],"start":140451711,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140451711,"alleles":["A","-"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140451714,"alleles":["AA","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451713,"clinical_significance":[],"seq_region_name":"7","id":"rs1158042395"},{"source":"dbSNP","start":140451717,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140451717,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1350233413","seq_region_name":"7"},{"seq_region_name":"7","id":"rs753466516","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451726,"source":"dbSNP","strand":1,"feature_type":"variation","end":140451726,"alleles":["C","T"]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451735,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140451735,"seq_region_name":"7","id":"rs1041626884","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1281471142","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451737,"feature_type":"variation","strand":1,"end":140451737,"alleles":["T","C"]},{"source":"dbSNP","start":140451740,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["AAAA","AA"],"end":140451743,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs762194528"},{"source":"dbSNP","start":140451741,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140451741,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1327313810","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140451746,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451746,"source":"dbSNP","seq_region_name":"7","id":"rs1298167114","clinical_significance":[]},{"source":"dbSNP","start":140451750,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140451750,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1380930671"},{"feature_type":"variation","strand":1,"end":140451751,"alleles":["T","C","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451751,"clinical_significance":[],"seq_region_name":"7","id":"rs1384826231"},{"clinical_significance":[],"id":"rs907165353","seq_region_name":"7","source":"dbSNP","start":140451754,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140451754,"feature_type":"variation","strand":1},{"start":140451756,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140451756,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1407573067","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794339642","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451757,"feature_type":"variation","strand":1,"end":140451757,"alleles":["C","T"]},{"start":140451758,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","C","G"],"end":140451758,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1002743551","clinical_significance":[]},{"seq_region_name":"7","id":"rs1477485591","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451760,"source":"dbSNP","strand":1,"feature_type":"variation","end":140451763,"alleles":["ACAC","AC"]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451761,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140451761,"clinical_significance":[],"seq_region_name":"7","id":"rs1373343414"},{"start":140451766,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","A","T"],"end":140451766,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1056492113","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs564407195","end":140451767,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140451767,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794339937","source":"dbSNP","start":140451768,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140451768,"alleles":["C","A"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140451769,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140451769,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1204155129"},{"seq_region_name":"7","id":"rs1794340030","clinical_significance":[],"start":140451770,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140451770,"strand":1,"feature_type":"variation"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451772,"feature_type":"variation","strand":1,"end":140451772,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs895126264"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585455491","end":140451773,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140451773,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"alleles":["C","A"],"end":140451775,"feature_type":"variation","strand":1,"source":"dbSNP","start":140451775,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130223290"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1012346372","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451778,"feature_type":"variation","strand":1,"alleles":["G","C","T"],"end":140451778},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451781,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140451781,"seq_region_name":"7","id":"rs1340288684","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451785,"source":"dbSNP","strand":1,"feature_type":"variation","end":140451785,"alleles":["C","G"],"seq_region_name":"7","id":"rs1794340226","clinical_significance":[]},{"seq_region_name":"7","id":"rs1253337219","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451786,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140451786},{"seq_region_name":"7","id":"rs1585455498","clinical_significance":[],"start":140451788,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140451788,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1028113201","alleles":["C","A"],"end":140451795,"feature_type":"variation","strand":1,"source":"dbSNP","start":140451795,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1042025063","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451798,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140451798},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451800,"feature_type":"variation","strand":1,"end":140451800,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs952197969"},{"end":140451802,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140451802,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1280649181","clinical_significance":[]},{"alleles":["C","T"],"end":140451804,"feature_type":"variation","strand":1,"source":"dbSNP","start":140451804,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs531859059"},{"end":140451807,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140451807,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1794340458","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1455052567","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451809,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140451809},{"alleles":["T","C"],"end":140451810,"feature_type":"variation","strand":1,"source":"dbSNP","start":140451810,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs543449796","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1334095484","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451811,"feature_type":"variation","strand":1,"alleles":["ATC","ATCATC"],"end":140451813},{"strand":1,"feature_type":"variation","end":140451813,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451813,"source":"dbSNP","seq_region_name":"7","id":"rs1396632457","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451813,"feature_type":"variation","strand":1,"end":140451817,"alleles":["CCCCC","CCCCCCC"],"clinical_significance":[],"seq_region_name":"7","id":"rs1055892933"},{"start":140451814,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140451814,"alleles":["C","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1169236504","clinical_significance":[]},{"source":"dbSNP","start":140451815,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140451815,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794340644"},{"end":140451821,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140451821,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1794340664","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451823,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140451823,"seq_region_name":"7","id":"rs774115185","clinical_significance":[]},{"end":140451826,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140451826,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794340723"},{"seq_region_name":"7","id":"rs1284067547","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451826,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TT","T"],"end":140451827},{"source":"dbSNP","start":140451838,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140451838,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs561786264"},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140451840,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451840,"source":"dbSNP","seq_region_name":"7","id":"rs1585455539","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140451841,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451841,"source":"dbSNP","seq_region_name":"7","id":"rs1184043861","clinical_significance":[]},{"seq_region_name":"7","id":"rs529260004","clinical_significance":[],"start":140451847,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140451847,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs10269611","seq_region_name":"7","alleles":["G","A","C","T"],"end":140451848,"feature_type":"variation","strand":1,"source":"dbSNP","start":140451848,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451850,"source":"dbSNP","strand":1,"feature_type":"variation","end":140451850,"alleles":["T","C"],"seq_region_name":"7","id":"rs1794340975","clinical_significance":[]},{"source":"dbSNP","start":140451851,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140451851,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1563083375"},{"alleles":["T","C"],"end":140451856,"feature_type":"variation","strand":1,"source":"dbSNP","start":140451856,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130223518"},{"alleles":["C","G","T"],"end":140451859,"strand":1,"feature_type":"variation","start":140451859,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs186125428","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794341047","clinical_significance":[],"start":140451861,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140451861,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs989920614","source":"dbSNP","start":140451863,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140451863,"alleles":["T","A","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs914290286","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451867,"feature_type":"variation","strand":1,"end":140451867,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794341143","end":140451868,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140451868,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1794341167","seq_region_name":"7","source":"dbSNP","start":140451870,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140451870,"alleles":["A","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs945793912","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451872,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140451872},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794341205","end":140451873,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140451873,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"end":140451882,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140451882,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585455574"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451887,"source":"dbSNP","strand":1,"feature_type":"variation","end":140451887,"alleles":["T","A"],"seq_region_name":"7","id":"rs1194236341","clinical_significance":[]},{"end":140451889,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140451889,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1341808175","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794341308","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451890,"source":"dbSNP","strand":1,"feature_type":"variation","end":140451890,"alleles":["A","G"]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451893,"feature_type":"variation","strand":1,"alleles":["T","TT"],"end":140451893,"clinical_significance":[],"seq_region_name":"7","id":"rs1292946162"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451895,"feature_type":"variation","strand":1,"end":140451895,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585455584"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794341378","source":"dbSNP","start":140451898,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140451898,"alleles":["G","C"],"feature_type":"variation","strand":1},{"start":140451899,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","A"],"end":140451899,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794341401","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451903,"feature_type":"variation","strand":1,"end":140451903,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794341427"},{"start":140451904,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A","T"],"end":140451904,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794341444","clinical_significance":[]},{"clinical_significance":[],"id":"rs1794341480","seq_region_name":"7","source":"dbSNP","start":140451904,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","-"],"end":140451904,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1041574616","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451907,"source":"dbSNP","strand":1,"feature_type":"variation","end":140451907,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1794341527","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140451908,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451908,"source":"dbSNP"},{"start":140451910,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140451910,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs1794341554","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451913,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140451913,"id":"rs1248691265","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1357887231","source":"dbSNP","start":140451914,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140451914,"alleles":["C","A","T"],"feature_type":"variation","strand":1},{"alleles":["C","A"],"end":140451915,"strand":1,"feature_type":"variation","start":140451915,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1794341622","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451917,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140451917,"id":"rs765033409","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451918,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140451918,"clinical_significance":[],"id":"rs928453119","seq_region_name":"7"},{"alleles":["TT","TTT"],"end":140451919,"strand":1,"feature_type":"variation","start":140451918,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1467645734","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140451920,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451920,"clinical_significance":[],"seq_region_name":"7","id":"rs938642607"},{"clinical_significance":[],"id":"rs1335774457","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451922,"feature_type":"variation","strand":1,"end":140451922,"alleles":["C","T"]},{"end":140451926,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140451926,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1794341766","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794341791","source":"dbSNP","start":140451926,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["CTCT","CT"],"end":140451929,"feature_type":"variation","strand":1},{"id":"rs1234554590","seq_region_name":"7","clinical_significance":[],"end":140451934,"alleles":["CCCC","CCC"],"strand":1,"feature_type":"variation","start":140451931,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"end":140451934,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140451934,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1794341851","clinical_significance":[]},{"id":"rs1794341878","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451936,"source":"dbSNP","strand":1,"feature_type":"variation","end":140451936,"alleles":["T","C"]},{"id":"rs1030992316","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140451939,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451939,"source":"dbSNP"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451942,"feature_type":"variation","strand":1,"end":140451942,"alleles":["T","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794341935"},{"end":140451945,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140451945,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130223747"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451946,"feature_type":"variation","strand":1,"alleles":["T","A","C","G"],"end":140451946,"clinical_significance":[],"seq_region_name":"7","id":"rs1369622294"},{"start":140451949,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140451949,"alleles":["C","A"],"strand":1,"feature_type":"variation","id":"rs1163955056","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1426356677","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140451954,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451954},{"clinical_significance":[],"seq_region_name":"7","id":"rs955074295","feature_type":"variation","strand":1,"end":140451957,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451957},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130223790","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451960,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140451960},{"clinical_significance":[],"seq_region_name":"7","id":"rs1056089854","feature_type":"variation","strand":1,"alleles":["G","C","T"],"end":140451963,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451963},{"start":140451967,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["GGTACACCTGAGGGTGGACTTAACTCCCCTGGGAGTTAG","GGTACACCTGAGGGTGGACTTAACTCCCCTGGGAGTTAGGTACACCTGAGGGTGGACTTAACTCCCCTGGGAGTTAG"],"end":140452005,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794342091","clinical_significance":[]},{"start":140451968,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","C"],"end":140451968,"strand":1,"feature_type":"variation","id":"rs1794342115","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794342141","clinical_significance":[],"start":140451969,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140451969,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1470476544","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451971,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140451971},{"clinical_significance":[],"seq_region_name":"7","id":"rs895168085","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451972,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140451972},{"seq_region_name":"7","id":"rs1794342220","clinical_significance":[],"end":140451973,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140451973,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"source":"dbSNP","start":140451974,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140451974,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1008268672"},{"start":140451975,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140451975,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs1794342277","seq_region_name":"7","clinical_significance":[]},{"id":"rs1386126136","seq_region_name":"7","clinical_significance":[],"start":140451979,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140451979,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140451980,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451980,"source":"dbSNP","seq_region_name":"7","id":"rs771480056","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs963793125","end":140451983,"alleles":["GG","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140451982,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1269921292","clinical_significance":[],"end":140452005,"alleles":["GGACTTAACTCCCCTGGGAGTTAG","GGACTTAACTCCCCTGGGAGTTAGGACTTAACTCCCCTGGGAGTTAG"],"strand":1,"feature_type":"variation","start":140451982,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140451983,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451983,"source":"dbSNP","seq_region_name":"7","id":"rs1794342407","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451985,"feature_type":"variation","strand":1,"end":140451985,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794342441"},{"alleles":["CTTAACTCCCC","-"],"end":140451995,"strand":1,"feature_type":"variation","start":140451985,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1176524269","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1489947858","source":"dbSNP","start":140451986,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140451986,"alleles":["T","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs554697612","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140451988,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140451988,"source":"dbSNP"},{"start":140451989,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["ACTCCCCTGGGA","A"],"end":140452000,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794342602","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130223912","source":"dbSNP","start":140451991,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140451991,"alleles":["T","A"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140451992,"alleles":["C","A","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140451992,"clinical_significance":[],"id":"rs551987571","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1021453089","source":"dbSNP","start":140451996,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140451996,"alleles":["T","-"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs2130223931","clinical_significance":[],"start":140451996,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140451996,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1049050359","clinical_significance":[],"end":140452006,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140452006,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140452010,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452010,"clinical_significance":[],"seq_region_name":"7","id":"rs1353553655"},{"clinical_significance":[],"id":"rs967610664","seq_region_name":"7","end":140452011,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140452011,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140452013,"alleles":["GGG","GGGG"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452011,"source":"dbSNP","seq_region_name":"7","id":"rs375091291","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794342914","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452012,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140452012},{"end":140452013,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140452013,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1794342968","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140452015,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452015,"clinical_significance":[],"seq_region_name":"7","id":"rs1392467490"},{"id":"rs1794343060","seq_region_name":"7","clinical_significance":[],"start":140452016,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140452016,"alleles":["A","AA"],"strand":1,"feature_type":"variation"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452018,"feature_type":"variation","strand":1,"end":140452019,"alleles":["AA","AAA"],"clinical_significance":[],"id":"rs1794343103","seq_region_name":"7"},{"source":"dbSNP","start":140452027,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140452027,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs977376257"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1303335763","feature_type":"variation","strand":1,"end":140452027,"alleles":["G","-"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452027},{"clinical_significance":[],"seq_region_name":"7","id":"rs1322730470","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452031,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140452031},{"seq_region_name":"7","id":"rs928504564","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","AA"],"end":140452032,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452032,"source":"dbSNP"},{"source":"dbSNP","start":140452032,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140452032,"alleles":["A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1563083436"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1401208230","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452035,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140452035},{"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140452046,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452046,"source":"dbSNP","id":"rs1794343396","seq_region_name":"7","clinical_significance":[]},{"start":140452048,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","A","C"],"end":140452048,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs775071202","clinical_significance":[]},{"clinical_significance":[],"id":"rs938716132","seq_region_name":"7","source":"dbSNP","start":140452049,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140452049,"alleles":["G","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1410137733","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452049,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GG","G"],"end":140452050},{"strand":1,"feature_type":"variation","end":140452052,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452052,"source":"dbSNP","seq_region_name":"7","id":"rs1337588224","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452053,"feature_type":"variation","strand":1,"end":140452056,"alleles":["CCCC","CCC"],"clinical_significance":[],"seq_region_name":"7","id":"rs1563083451"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452054,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140452054,"seq_region_name":"7","id":"rs2130224093","clinical_significance":[]},{"clinical_significance":[],"id":"rs991457417","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140452058,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452058},{"seq_region_name":"7","id":"rs1440701834","clinical_significance":[],"alleles":["GTTGTT","GTT"],"end":140452063,"strand":1,"feature_type":"variation","start":140452058,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1794343709","clinical_significance":[],"start":140452061,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140452061,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452062,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140452062,"seq_region_name":"7","id":"rs1279481887","clinical_significance":[]},{"source":"dbSNP","start":140452063,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140452063,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1794343790","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs761030972","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452065,"feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140452065},{"seq_region_name":"7","id":"rs1794343907","clinical_significance":[],"start":140452066,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140452066,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794343947","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452067,"feature_type":"variation","strand":1,"end":140452067,"alleles":["A","C"]},{"feature_type":"variation","strand":1,"end":140452068,"alleles":["T","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452068,"clinical_significance":[],"id":"rs1246484274","seq_region_name":"7"},{"source":"dbSNP","start":140452072,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140452072,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130224154"},{"end":140452076,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140452076,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1004953396","clinical_significance":[]},{"id":"rs2130224162","seq_region_name":"7","clinical_significance":[],"start":140452077,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140452077,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs34444523","feature_type":"variation","strand":1,"end":140452080,"alleles":["TATA","TA","TATATA"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452077},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585455748","source":"dbSNP","start":140452078,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140452078,"alleles":["A","G"],"feature_type":"variation","strand":1},{"end":140452079,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140452079,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1794344274","seq_region_name":"7","clinical_significance":[]},{"start":140452084,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","A"],"end":140452084,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130224208","clinical_significance":[]},{"source":"dbSNP","start":140452086,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140452086,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1291093710"},{"seq_region_name":"7","id":"rs1282815127","clinical_significance":[],"end":140452088,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140452088,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"feature_type":"variation","strand":1,"end":140452090,"alleles":["A","AA"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452090,"clinical_significance":[],"seq_region_name":"7","id":"rs1208682679"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794344395","source":"dbSNP","start":140452090,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140452090,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452093,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140452093,"seq_region_name":"7","id":"rs191350890","clinical_significance":[]},{"clinical_significance":[],"id":"rs1283378921","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140452098,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452098},{"seq_region_name":"7","id":"rs901982783","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452105,"source":"dbSNP","strand":1,"feature_type":"variation","end":140452105,"alleles":["A","G"]},{"clinical_significance":[],"id":"rs1794344583","seq_region_name":"7","end":140452106,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140452106,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452111,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AAA","AA"],"end":140452113,"seq_region_name":"7","id":"rs1794344620","clinical_significance":[]},{"source":"dbSNP","start":140452115,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140452115,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794344670"},{"start":140452117,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140452117,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794344701","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452119,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140452119,"seq_region_name":"7","id":"rs1794344736","clinical_significance":[]},{"end":140452121,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140452121,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1195998337","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794344822","end":140452122,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140452122,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1794344862","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452124,"source":"dbSNP","strand":1,"feature_type":"variation","end":140452124,"alleles":["T","C"]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452125,"source":"dbSNP","strand":1,"feature_type":"variation","end":140452125,"alleles":["A","T"],"seq_region_name":"7","id":"rs1794344901","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794344940","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452126,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140452126},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140452129,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452129,"source":"dbSNP","seq_region_name":"7","id":"rs1274556060","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452133,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140452133,"seq_region_name":"7","id":"rs1794345033","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140452144,"alleles":["GAGTTGGAGT","GAGT"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452135,"source":"dbSNP","id":"rs1365125381","seq_region_name":"7","clinical_significance":[]},{"id":"rs898027781","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452138,"source":"dbSNP","strand":1,"feature_type":"variation","end":140452139,"alleles":["TT","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794345161","source":"dbSNP","start":140452139,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140452139,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452141,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140452141,"seq_region_name":"7","id":"rs1431257903","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452144,"source":"dbSNP","strand":1,"feature_type":"variation","end":140452144,"alleles":["T","C"],"seq_region_name":"7","id":"rs764686881","clinical_significance":[]},{"end":140452147,"alleles":["TT","TTT"],"strand":1,"feature_type":"variation","start":140452146,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1794345249","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794345273","clinical_significance":[],"start":140452147,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140452147,"alleles":["T","C","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs997795333","seq_region_name":"7","end":140452155,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140452155,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs553002904","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140452156,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452156},{"id":"rs1236507912","seq_region_name":"7","clinical_significance":[],"start":140452158,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","G"],"end":140452158,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs141698092","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452161,"source":"dbSNP","strand":1,"feature_type":"variation","end":140452161,"alleles":["G","C","T"]},{"end":140452163,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140452163,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585455810"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452164,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140452164,"id":"rs1185475675","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452165,"feature_type":"variation","strand":1,"alleles":["A","C","G","T"],"end":140452165,"clinical_significance":[],"id":"rs1017919582","seq_region_name":"7"},{"seq_region_name":"7","id":"rs377701825","clinical_significance":[],"end":140452167,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140452167,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452170,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140452170,"clinical_significance":[],"id":"rs1794346779","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140452171,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452171,"source":"dbSNP","seq_region_name":"7","id":"rs1472619991","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585455826","clinical_significance":[],"alleles":["G","A"],"end":140452176,"strand":1,"feature_type":"variation","start":140452176,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"alleles":["C","T"],"end":140452177,"feature_type":"variation","strand":1,"source":"dbSNP","start":140452177,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs765643222"},{"end":140452178,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140452178,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs373595652","clinical_significance":[]},{"clinical_significance":[],"id":"rs1021297754","seq_region_name":"7","alleles":["T","A"],"end":140452182,"feature_type":"variation","strand":1,"source":"dbSNP","start":140452182,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"end":140452185,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140452185,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794346974"},{"source":"dbSNP","start":140452188,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140452209,"alleles":["CTCACGCCACTCTCCTGCCTCA","CTCACGCCACTCTCCTGCCTCACGCCACTCTCCTGCCTCA"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1240739711"},{"strand":1,"feature_type":"variation","end":140452192,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452192,"source":"dbSNP","seq_region_name":"7","id":"rs750627226","clinical_significance":[]},{"alleles":["G","A"],"end":140452193,"feature_type":"variation","strand":1,"source":"dbSNP","start":140452193,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs777562505","seq_region_name":"7"},{"alleles":["C","G"],"end":140452194,"feature_type":"variation","strand":1,"source":"dbSNP","start":140452194,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794347092"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794347120","end":140452195,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140452195,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1585455847","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452196,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140452196},{"alleles":["C","T"],"end":140452197,"feature_type":"variation","strand":1,"source":"dbSNP","start":140452197,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1554445604"},{"source":"dbSNP","start":140452202,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140452202,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130224495"},{"seq_region_name":"7","id":"rs1263207973","clinical_significance":[],"start":140452204,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140452204,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1794347231","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452205,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140452205},{"end":140452209,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140452209,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs568010144","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452212,"feature_type":"variation","strand":1,"end":140452212,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1307967940"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794347331","alleles":["C","T"],"end":140452214,"feature_type":"variation","strand":1,"source":"dbSNP","start":140452214,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452214,"source":"dbSNP","strand":1,"feature_type":"variation","end":140452216,"alleles":["CCC","CC"],"seq_region_name":"7","id":"rs1794347354","clinical_significance":[]},{"source":"dbSNP","start":140452215,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140452215,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs928485783"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1277432605","source":"dbSNP","start":140452216,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140452216,"feature_type":"variation","strand":1},{"id":"rs938491231","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140452217,"strand":1,"feature_type":"variation","start":140452217,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"alleles":["T","C"],"end":140452220,"feature_type":"variation","strand":1,"source":"dbSNP","start":140452220,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs187085725"},{"end":140452223,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140452223,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1291879023","clinical_significance":[]},{"seq_region_name":"7","id":"rs915846424","clinical_significance":[],"alleles":["G","A","C"],"end":140452227,"strand":1,"feature_type":"variation","start":140452227,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1355195101","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452229,"feature_type":"variation","strand":1,"end":140452229,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794348326","alleles":["G","A"],"end":140452231,"feature_type":"variation","strand":1,"source":"dbSNP","start":140452231,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452234,"feature_type":"variation","strand":1,"end":140452234,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs991383708"},{"end":140452235,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140452235,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1383511424"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452236,"feature_type":"variation","strand":1,"alleles":["G","C","T"],"end":140452236,"clinical_significance":[],"seq_region_name":"7","id":"rs931241788"},{"seq_region_name":"7","id":"rs1585455886","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140452237,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452237,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140452238,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452238,"source":"dbSNP","seq_region_name":"7","id":"rs1358684247","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794348602","source":"dbSNP","start":140452238,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["CCC","CC"],"end":140452240,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1171334295","clinical_significance":[],"start":140452240,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140452240,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140452241,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140452241,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1794348640","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1227800794","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452243,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140452243},{"feature_type":"variation","strand":1,"end":140452246,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452246,"clinical_significance":[],"seq_region_name":"7","id":"rs1417725696"},{"seq_region_name":"7","id":"rs1794348751","clinical_significance":[],"start":140452247,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140452247,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1168416063","end":140452248,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140452248,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140452250,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452250,"clinical_significance":[],"seq_region_name":"7","id":"rs1445746486"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794348858","end":140452251,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140452251,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"start":140452253,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140452253,"alleles":["A","T"],"strand":1,"feature_type":"variation","id":"rs1794348899","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140452255,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452255,"clinical_significance":[],"id":"rs1245556083","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452257,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140452257,"seq_region_name":"7","id":"rs915951315","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452258,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140452258,"seq_region_name":"7","id":"rs1481962346","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794349237","alleles":["T","C"],"end":140452263,"feature_type":"variation","strand":1,"source":"dbSNP","start":140452263,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1585455913","clinical_significance":[],"end":140452265,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140452265,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1236401843","feature_type":"variation","strand":1,"end":140452266,"alleles":["T","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452266},{"strand":1,"feature_type":"variation","end":140452267,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452267,"source":"dbSNP","seq_region_name":"7","id":"rs1794349353","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452271,"feature_type":"variation","strand":1,"end":140452271,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs942002250"},{"clinical_significance":[],"seq_region_name":"7","id":"rs973493066","end":140452272,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140452272,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1049112425","source":"dbSNP","start":140452273,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140452273,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452274,"source":"dbSNP","strand":1,"feature_type":"variation","end":140452274,"alleles":["G","A"],"seq_region_name":"7","id":"rs1272193250","clinical_significance":[]},{"id":"rs1336900296","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["AGAGA","AGA"],"end":140452280,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452276,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1213405063","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452277,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140452277},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452279,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140452279,"clinical_significance":[],"seq_region_name":"7","id":"rs867074038"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452280,"feature_type":"variation","strand":1,"end":140452280,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794349971"},{"source":"dbSNP","start":140452281,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140452281,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794350022"},{"strand":1,"feature_type":"variation","end":140452282,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452282,"source":"dbSNP","id":"rs1486581061","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140452284,"alleles":["G","A","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452284,"clinical_significance":[],"seq_region_name":"7","id":"rs940768226"},{"end":140452290,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140452290,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794350179"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794350228","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140452292,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452292},{"id":"rs1298820337","seq_region_name":"7","clinical_significance":[],"end":140452293,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140452293,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"start":140452298,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140452298,"strand":1,"feature_type":"variation","id":"rs1794350282","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794350316","clinical_significance":[],"start":140452302,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140452302,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs929508223","source":"dbSNP","start":140452303,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140452303,"alleles":["G","C"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140452304,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452304,"source":"dbSNP","id":"rs1036423583","seq_region_name":"7","clinical_significance":[]},{"end":140452308,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140452308,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1794350423","clinical_significance":[]},{"seq_region_name":"7","id":"rs1256589565","clinical_significance":[],"start":140452309,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["TCTCGATCTCCTGACCTC","TC"],"end":140452326,"strand":1,"feature_type":"variation"},{"end":140452312,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140452312,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs191935426","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794350589","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452313,"feature_type":"variation","strand":1,"end":140452313,"alleles":["G","A"]},{"start":140452314,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","C","G"],"end":140452314,"strand":1,"feature_type":"variation","id":"rs1194235909","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","-"],"end":140452315,"feature_type":"variation","strand":1,"source":"dbSNP","start":140452315,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1794350677","seq_region_name":"7"},{"start":140452316,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140452316,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794350715","clinical_significance":[]},{"clinical_significance":[],"id":"rs1794350759","seq_region_name":"7","source":"dbSNP","start":140452317,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140452317,"alleles":["T","C"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140452320,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140452320,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794350799"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585455976","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452322,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140452322},{"start":140452324,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140452324,"alleles":["C","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs182912780","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140452326,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452326,"source":"dbSNP","seq_region_name":"7","id":"rs1029155075","clinical_significance":[]},{"end":140452327,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140452327,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1412439975"},{"seq_region_name":"7","id":"rs1481397838","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452333,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140452333},{"feature_type":"variation","strand":1,"end":140452334,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452334,"clinical_significance":[],"seq_region_name":"7","id":"rs889405495"},{"start":140452337,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140452337,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","id":"rs545657315","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1021276515","source":"dbSNP","start":140452338,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140452338,"alleles":["G","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs2130224891","clinical_significance":[],"alleles":["C","T"],"end":140452339,"strand":1,"feature_type":"variation","start":140452339,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452342,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140452342,"seq_region_name":"7","id":"rs557979233","clinical_significance":[]},{"source":"dbSNP","start":140452343,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140452343,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs977161185"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794351317","feature_type":"variation","strand":1,"end":140452344,"alleles":["-","AT"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452345},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452345,"feature_type":"variation","strand":1,"end":140452345,"alleles":["C","G"],"clinical_significance":[],"id":"rs1307773912","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1794351381","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140452347,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452347,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1794351418","clinical_significance":[],"start":140452349,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140452349,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140452351,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452351,"source":"dbSNP","id":"rs1794351455","seq_region_name":"7","clinical_significance":[]},{"end":140452353,"alleles":["AAA","A"],"strand":1,"feature_type":"variation","start":140452351,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1794351496","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","G"],"end":140452352,"strand":1,"feature_type":"variation","start":140452352,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1225579750","seq_region_name":"7","clinical_significance":[]},{"id":"rs1794351567","seq_region_name":"7","clinical_significance":[],"start":140452353,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140452353,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1348745885","clinical_significance":[],"end":140452354,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140452354,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140452357,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452357,"source":"dbSNP","seq_region_name":"7","id":"rs1794351653","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140452358,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452358,"clinical_significance":[],"id":"rs1794351692","seq_region_name":"7"},{"end":140452364,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140452364,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1039254287","clinical_significance":[]},{"clinical_significance":[],"id":"rs1794351767","seq_region_name":"7","alleles":["C","A","G"],"end":140452366,"feature_type":"variation","strand":1,"source":"dbSNP","start":140452366,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs576449824","alleles":["G","A"],"end":140452369,"feature_type":"variation","strand":1,"source":"dbSNP","start":140452369,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140452370,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140452370,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs543858810"},{"seq_region_name":"7","id":"rs1011158644","clinical_significance":[],"start":140452371,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140452371,"alleles":["G","A","C"],"strand":1,"feature_type":"variation"},{"id":"rs959808008","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452373,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140452373},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794352033","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452374,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140452374},{"seq_region_name":"7","id":"rs1794352066","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452375,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140452375},{"seq_region_name":"7","id":"rs1794352112","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452376,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140452376},{"id":"rs991769754","seq_region_name":"7","clinical_significance":[],"start":140452377,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140452377,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"start":140452379,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140452379,"alleles":["C","G"],"strand":1,"feature_type":"variation","id":"rs915725043","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs368041438","clinical_significance":[],"start":140452381,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140452381,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452382,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140452382,"clinical_significance":[],"seq_region_name":"7","id":"rs529223658"},{"source":"dbSNP","start":140452384,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140452384,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794352338"},{"seq_region_name":"7","id":"rs541044504","clinical_significance":[],"strand":1,"feature_type":"variation","end":140452386,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452386,"source":"dbSNP"},{"start":140452387,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140452387,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1409157405","clinical_significance":[]},{"source":"dbSNP","start":140452389,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140452389,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs998600185","seq_region_name":"7"},{"clinical_significance":[],"id":"rs902904509","seq_region_name":"7","feature_type":"variation","strand":1,"end":140452393,"alleles":["CCCCC","CCCCCC"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452389},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452393,"feature_type":"variation","strand":1,"end":140452393,"alleles":["C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130225128"},{"alleles":["T","C"],"end":140452395,"feature_type":"variation","strand":1,"source":"dbSNP","start":140452395,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs376854792"},{"clinical_significance":[],"seq_region_name":"7","id":"rs559604851","feature_type":"variation","strand":1,"end":140452396,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452396},{"source":"dbSNP","start":140452397,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140452397,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1232079270","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs909230577","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452400,"feature_type":"variation","strand":1,"end":140452400,"alleles":["C","A","G","T"]},{"start":140452404,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["TTCTTT","TT"],"end":140452409,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs959895636","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140452405,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452405,"source":"dbSNP","id":"rs940631733","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140452406,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452406,"source":"dbSNP","seq_region_name":"7","id":"rs1036456953","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794352887","alleles":["T","C"],"end":140452407,"feature_type":"variation","strand":1,"source":"dbSNP","start":140452407,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"alleles":["TTT","TTTT"],"end":140452409,"strand":1,"feature_type":"variation","start":140452407,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1224351450","clinical_significance":[]},{"clinical_significance":[],"id":"rs1279504863","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140452408,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452408},{"strand":1,"feature_type":"variation","end":140452409,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452409,"source":"dbSNP","id":"rs758710785","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1206635167","clinical_significance":[],"end":140452411,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140452411,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"alleles":["TTTTTTT","TTTTTT","TTTTTTTT"],"end":140452417,"strand":1,"feature_type":"variation","start":140452411,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1363130573","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs533710252","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452416,"source":"dbSNP","strand":1,"feature_type":"variation","end":140452416,"alleles":["T","C"]},{"end":140452422,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140452422,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1794354927","clinical_significance":[]},{"alleles":["A","G"],"end":140452424,"feature_type":"variation","strand":1,"source":"dbSNP","start":140452424,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794354970"},{"clinical_significance":[],"seq_region_name":"7","id":"rs766300628","source":"dbSNP","start":140452426,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140452426,"alleles":["T","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1794355388","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140452428,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452428,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1051056857","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452434,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140452434},{"source":"dbSNP","start":140452436,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140452436,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1385715953"},{"id":"rs889280413","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140452442,"strand":1,"feature_type":"variation","start":140452442,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"end":140452443,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140452443,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794355564"},{"strand":1,"feature_type":"variation","end":140452444,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452444,"source":"dbSNP","seq_region_name":"7","id":"rs1585456076","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1157858102","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140452445,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452445},{"clinical_significance":[],"id":"rs1794355683","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140452446,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452446},{"seq_region_name":"7","id":"rs1794355729","clinical_significance":[],"strand":1,"feature_type":"variation","end":140452459,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452459,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452465,"source":"dbSNP","strand":1,"feature_type":"variation","end":140452465,"alleles":["G","A","C"],"seq_region_name":"7","id":"rs1469981158","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140452474,"alleles":["A","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452474,"clinical_significance":[],"seq_region_name":"7","id":"rs1585456083"},{"clinical_significance":[],"id":"rs1196347374","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452479,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140452479},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794355914","feature_type":"variation","strand":1,"end":140452481,"alleles":["A","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452481},{"clinical_significance":[],"seq_region_name":"7","id":"rs1011799353","alleles":["C","T"],"end":140452482,"feature_type":"variation","strand":1,"source":"dbSNP","start":140452482,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1445545051","clinical_significance":[],"start":140452483,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140452483,"strand":1,"feature_type":"variation"},{"end":140452492,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140452492,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs751670833"},{"end":140452493,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140452493,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs902860711","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794356092","clinical_significance":[],"start":140452494,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140452494,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1794356120","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452496,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140452496},{"feature_type":"variation","strand":1,"end":140452498,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452498,"clinical_significance":[],"seq_region_name":"7","id":"rs75842984"},{"start":140452499,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","A","C"],"end":140452499,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1267572797","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794356337","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140452501,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452501},{"end":140452506,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140452506,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1204443780","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452513,"source":"dbSNP","strand":1,"feature_type":"variation","end":140452513,"alleles":["C","T"],"seq_region_name":"7","id":"rs541842895","clinical_significance":[]},{"end":140452514,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140452514,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs371839327","seq_region_name":"7"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452516,"feature_type":"variation","strand":1,"end":140452516,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1205558643"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452518,"feature_type":"variation","strand":1,"end":140452518,"alleles":["T","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1325887316"},{"seq_region_name":"7","id":"rs973378548","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452522,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140452522},{"seq_region_name":"7","id":"rs1794356697","clinical_significance":[],"strand":1,"feature_type":"variation","end":140452524,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452524,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452526,"source":"dbSNP","strand":1,"feature_type":"variation","end":140452526,"alleles":["T","G"],"seq_region_name":"7","id":"rs148571030","clinical_significance":[]},{"source":"dbSNP","start":140452527,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140452527,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794356841"},{"seq_region_name":"7","id":"rs960081273","clinical_significance":[],"end":140452529,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140452529,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"strand":1,"feature_type":"variation","end":140452533,"alleles":["C","A","G","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452533,"source":"dbSNP","seq_region_name":"7","id":"rs756112343","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140452534,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452534,"clinical_significance":[],"id":"rs1794357045","seq_region_name":"7"},{"alleles":["G","-"],"end":140452534,"feature_type":"variation","strand":1,"source":"dbSNP","start":140452534,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794357080"},{"strand":1,"feature_type":"variation","end":140452536,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452536,"source":"dbSNP","seq_region_name":"7","id":"rs1433517281","clinical_significance":[]},{"seq_region_name":"7","id":"rs1365174855","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452537,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140452537},{"end":140452538,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140452538,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs187544453","clinical_significance":[]},{"seq_region_name":"7","id":"rs952552897","clinical_significance":[],"alleles":["C","A","T"],"end":140452543,"strand":1,"feature_type":"variation","start":140452543,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs112952207","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452544,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140452544},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140452546,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452546,"source":"dbSNP","seq_region_name":"7","id":"rs1585456163","clinical_significance":[]},{"start":140452547,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140452547,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794357498","clinical_significance":[]},{"seq_region_name":"7","id":"rs1170390114","clinical_significance":[],"start":140452551,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140452551,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140452552,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140452552,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs568176012"},{"seq_region_name":"7","id":"rs546007148","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452554,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140452554},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452555,"source":"dbSNP","strand":1,"feature_type":"variation","end":140452555,"alleles":["T","G"],"id":"rs778919658","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130225746","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452560,"source":"dbSNP","strand":1,"feature_type":"variation","end":140452560,"alleles":["T","C"]},{"strand":1,"feature_type":"variation","end":140452570,"alleles":["TAACATAA","TAA"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452563,"source":"dbSNP","seq_region_name":"7","id":"rs1170319522","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140452567,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452567,"source":"dbSNP","id":"rs1039265702","seq_region_name":"7","clinical_significance":[]},{"alleles":["ATA","A"],"end":140452569,"strand":1,"feature_type":"variation","start":140452567,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1794358181","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1247386425","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452569,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140452569},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452570,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140452570,"seq_region_name":"7","id":"rs961278123","clinical_significance":[]},{"seq_region_name":"7","id":"rs1444154475","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140452575,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452575,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1254183665","clinical_significance":[],"start":140452576,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140452576,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs972099701","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452581,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140452581},{"clinical_significance":[],"seq_region_name":"7","id":"rs923279152","end":140452582,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140452582,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1253432377","clinical_significance":[],"strand":1,"feature_type":"variation","end":140452584,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452584,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140452585,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452585,"clinical_significance":[],"seq_region_name":"7","id":"rs1794358777"},{"seq_region_name":"7","id":"rs947069532","clinical_significance":[],"end":140452588,"alleles":["C","A","G"],"strand":1,"feature_type":"variation","start":140452588,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"end":140452601,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140452601,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1316291007","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794359045","source":"dbSNP","start":140452604,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140452604,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140452605,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140452605,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs933429851"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452606,"source":"dbSNP","strand":1,"feature_type":"variation","end":140452606,"alleles":["T","C"],"seq_region_name":"7","id":"rs1248824319","clinical_significance":[]},{"alleles":["A","G"],"end":140452609,"feature_type":"variation","strand":1,"source":"dbSNP","start":140452609,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1372612505"},{"seq_region_name":"7","id":"rs1341672793","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140452612,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452612,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452614,"source":"dbSNP","strand":1,"feature_type":"variation","end":140452614,"alleles":["A","G"],"id":"rs1331706990","seq_region_name":"7","clinical_significance":[]},{"id":"rs1794359516","seq_region_name":"7","clinical_significance":[],"start":140452615,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140452615,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"start":140452617,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C","G"],"end":140452617,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794359581","clinical_significance":[]},{"alleles":["A","G"],"end":140452624,"feature_type":"variation","strand":1,"source":"dbSNP","start":140452624,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794359665"},{"seq_region_name":"7","id":"rs1794359720","clinical_significance":[],"start":140452629,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140452629,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140452632,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452632,"clinical_significance":[],"seq_region_name":"7","id":"rs1395077366"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794359870","feature_type":"variation","strand":1,"alleles":["T","A"],"end":140452635,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452635},{"id":"rs1396832147","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452636,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140452636},{"seq_region_name":"7","id":"rs1794359991","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452639,"source":"dbSNP","strand":1,"feature_type":"variation","end":140452639,"alleles":["A","C","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794360117","alleles":["G","C"],"end":140452640,"feature_type":"variation","strand":1,"source":"dbSNP","start":140452640,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"id":"rs535424729","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140452641,"alleles":["T","C","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452641,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130226155","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452642,"feature_type":"variation","strand":1,"end":140452642,"alleles":["A","G"]},{"end":140452643,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140452643,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs910732038","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs147297546","source":"dbSNP","start":140452657,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["ACTCAC","AC"],"end":140452662,"feature_type":"variation","strand":1},{"end":140452658,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140452658,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1794360495","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140452661,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140452661,"alleles":["A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794360550"},{"clinical_significance":[],"id":"rs534244523","seq_region_name":"7","source":"dbSNP","start":140452663,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["AAAAAA","AAAAAAA"],"end":140452668,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452665,"source":"dbSNP","strand":1,"feature_type":"variation","end":140452665,"alleles":["A","C"],"seq_region_name":"7","id":"rs1164069418","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794360800","clinical_significance":[],"alleles":["T","C"],"end":140452670,"strand":1,"feature_type":"variation","start":140452670,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1056874246","clinical_significance":[],"start":140452674,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["AATAAT","AAT"],"end":140452679,"strand":1,"feature_type":"variation"},{"alleles":["A","G"],"end":140452675,"feature_type":"variation","strand":1,"source":"dbSNP","start":140452675,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1366789218"},{"start":140452677,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140452677,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794361007","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1258784688","feature_type":"variation","strand":1,"alleles":["CTCCT","CT"],"end":140452689,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452685},{"seq_region_name":"7","id":"rs1794361152","clinical_significance":[],"strand":1,"feature_type":"variation","end":140452686,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452686,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1585456345","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140452687,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452687,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1186999073","seq_region_name":"7","end":140452690,"alleles":["CTT","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140452688,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs895659237","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452691,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140452691},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452696,"source":"dbSNP","strand":1,"feature_type":"variation","end":140452696,"alleles":["T","C"],"id":"rs1794361436","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","C","G"],"end":140452697,"feature_type":"variation","strand":1,"source":"dbSNP","start":140452697,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs547443399"},{"id":"rs947520914","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140452700,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452700,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140452701,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452701,"source":"dbSNP","seq_region_name":"7","id":"rs565831017","clinical_significance":[]},{"clinical_significance":[],"id":"rs1585456378","seq_region_name":"7","end":140452704,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140452704,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140452709,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452709,"source":"dbSNP","seq_region_name":"7","id":"rs963261378","clinical_significance":[]},{"start":140452711,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","A","C","G"],"end":140452711,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs768940075","clinical_significance":[]},{"clinical_significance":[],"id":"rs1794362032","seq_region_name":"7","source":"dbSNP","start":140452712,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140452712,"feature_type":"variation","strand":1},{"end":140452714,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140452714,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794362097"},{"end":140452720,"alleles":["AACAA","AA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140452716,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794362165"},{"id":"rs539761618","seq_region_name":"7","clinical_significance":[],"end":140452720,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140452720,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"end":140452721,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140452721,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1713525939","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794362333","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452722,"source":"dbSNP","strand":1,"feature_type":"variation","end":140452723,"alleles":["AA","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs557776722","source":"dbSNP","start":140452724,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140452724,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs999043084","source":"dbSNP","start":140452736,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","A","G"],"end":140452736,"feature_type":"variation","strand":1},{"alleles":["T","C"],"end":140452739,"feature_type":"variation","strand":1,"source":"dbSNP","start":140452739,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585456409"},{"strand":1,"feature_type":"variation","alleles":["ATA","ATAATA"],"end":140452743,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452741,"source":"dbSNP","id":"rs547425491","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1057227549","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452742,"feature_type":"variation","strand":1,"end":140452742,"alleles":["T","C"]},{"id":"rs1794362797","seq_region_name":"7","clinical_significance":[],"start":140452745,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140452745,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs895454007","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452747,"feature_type":"variation","strand":1,"end":140452747,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1794362935","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452748,"source":"dbSNP","strand":1,"feature_type":"variation","end":140452748,"alleles":["G","A"]},{"start":140452750,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140452750,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794362980","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1407627647","feature_type":"variation","strand":1,"end":140452753,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452753},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452754,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CCCCC","CCCC"],"end":140452758,"seq_region_name":"7","id":"rs1794363089","clinical_significance":[]},{"end":140452755,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140452755,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130226704"},{"id":"rs73485145","seq_region_name":"7","clinical_significance":[],"start":140452758,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140452758,"alleles":["C","G","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs151123476","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452759,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140452759},{"clinical_significance":[],"seq_region_name":"7","id":"rs746563279","source":"dbSNP","start":140452761,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140452761,"alleles":["T","C"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140452763,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452763,"clinical_significance":[],"seq_region_name":"7","id":"rs1794363446"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794363520","source":"dbSNP","start":140452766,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140452766,"alleles":["A","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794363581","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452768,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140452768},{"id":"rs1794363648","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140452770,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452770,"source":"dbSNP"},{"end":140452772,"alleles":["A","G","T"],"strand":1,"feature_type":"variation","start":140452772,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1794363695","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140452777,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452777,"source":"dbSNP","id":"rs1362488032","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794363807","alleles":["CAAGTTCAA","CAAGTTCAAGTTCAA"],"end":140452786,"feature_type":"variation","strand":1,"source":"dbSNP","start":140452778,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"start":140452779,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","C"],"end":140452779,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1162706231","clinical_significance":[]},{"seq_region_name":"7","id":"rs748518859","clinical_significance":[],"end":140452781,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140452781,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1015434305","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452788,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140452788},{"seq_region_name":"7","id":"rs961308655","clinical_significance":[],"end":140452789,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140452789,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"id":"rs915399014","seq_region_name":"7","clinical_significance":[],"end":140452791,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140452791,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"id":"rs946991053","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452796,"feature_type":"variation","strand":1,"end":140452796,"alleles":["C","T"]},{"feature_type":"variation","strand":1,"end":140452798,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452798,"clinical_significance":[],"id":"rs73735252","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1585456512","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140452802,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452802,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140452803,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452803,"clinical_significance":[],"id":"rs1563083837","seq_region_name":"7"},{"id":"rs2130226981","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140452805,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452805,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130226990","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452806,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140452806},{"alleles":["A","G"],"end":140452809,"feature_type":"variation","strand":1,"source":"dbSNP","start":140452809,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794364404"},{"seq_region_name":"7","id":"rs1794364482","clinical_significance":[],"strand":1,"feature_type":"variation","end":140452810,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452810,"source":"dbSNP"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452814,"feature_type":"variation","strand":1,"end":140452814,"alleles":["C","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs371821190"},{"clinical_significance":[],"seq_region_name":"7","id":"rs141104734","feature_type":"variation","strand":1,"end":140452818,"alleles":["T","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452818},{"seq_region_name":"7","id":"rs934308551","clinical_significance":[],"end":140452819,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140452819,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"id":"rs1794364666","seq_region_name":"7","clinical_significance":[],"start":140452822,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140452822,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1794364739","clinical_significance":[],"start":140452827,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140452827,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"id":"rs1304771865","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140452828,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452828,"source":"dbSNP"},{"source":"dbSNP","start":140452829,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140452829,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1206260916","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140452834,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452834,"clinical_significance":[],"seq_region_name":"7","id":"rs531304010"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1329169595","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452839,"feature_type":"variation","strand":1,"end":140452839,"alleles":["C","T"]},{"source":"dbSNP","start":140452840,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140452840,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130227081"},{"end":140452842,"alleles":["A","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140452842,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1269483817"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452843,"source":"dbSNP","strand":1,"feature_type":"variation","end":140452843,"alleles":["G","C"],"id":"rs1794365723","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452843,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GCGT","-"],"end":140452846,"seq_region_name":"7","id":"rs1794365785","clinical_significance":[]},{"id":"rs1226185384","seq_region_name":"7","clinical_significance":[],"start":140452844,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140452844,"strand":1,"feature_type":"variation"},{"id":"rs193149517","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452845,"source":"dbSNP","strand":1,"feature_type":"variation","end":140452845,"alleles":["G","A"]},{"clinical_significance":[],"id":"rs1275194818","seq_region_name":"7","end":140452847,"alleles":["TT","TTT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140452846,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452848,"feature_type":"variation","strand":1,"end":140452848,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs541007727"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1438391783","feature_type":"variation","strand":1,"end":140452850,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452850},{"alleles":["C","T"],"end":140452851,"strand":1,"feature_type":"variation","start":140452851,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1794366157","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452854,"source":"dbSNP","strand":1,"feature_type":"variation","end":140452854,"alleles":["G","C"],"seq_region_name":"7","id":"rs777104732","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1233608609","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452854,"feature_type":"variation","strand":1,"alleles":["G","-"],"end":140452854},{"seq_region_name":"7","id":"rs1794366327","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452858,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140452858},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140452861,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452861,"clinical_significance":[],"id":"rs1794366395","seq_region_name":"7"},{"alleles":["T","C"],"end":140452862,"strand":1,"feature_type":"variation","start":140452862,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1794366476","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452869,"feature_type":"variation","strand":1,"end":140452869,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs910605310"},{"feature_type":"variation","strand":1,"end":140452874,"alleles":["T","A","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452874,"clinical_significance":[],"id":"rs947470225","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585456605","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452880,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140452880},{"feature_type":"variation","strand":1,"end":140452881,"alleles":["A","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452881,"clinical_significance":[],"seq_region_name":"7","id":"rs762360972"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452884,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140452884,"seq_region_name":"7","id":"rs1401225219","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794366961","clinical_significance":[],"end":140452887,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140452887,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs559370414","clinical_significance":[],"end":140452888,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140452888,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140452889,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452889,"clinical_significance":[],"seq_region_name":"7","id":"rs184431998"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794367305","source":"dbSNP","start":140452890,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140452890,"alleles":["G","A"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140452891,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452891,"clinical_significance":[],"seq_region_name":"7","id":"rs895544397"},{"clinical_significance":[],"id":"rs948547276","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452899,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140452899},{"clinical_significance":[],"id":"rs1794367516","seq_region_name":"7","alleles":["G","A"],"end":140452900,"feature_type":"variation","strand":1,"source":"dbSNP","start":140452900,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140452901,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140452901,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585456642"},{"clinical_significance":[],"id":"rs1794367615","seq_region_name":"7","source":"dbSNP","start":140452905,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140452905,"alleles":["C","T"],"feature_type":"variation","strand":1},{"alleles":["TTT","T"],"end":140452909,"strand":1,"feature_type":"variation","start":140452907,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs2130227371","seq_region_name":"7","clinical_significance":[]},{"start":140452908,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140452915,"alleles":["TTCTCTCT","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794367690","clinical_significance":[]},{"start":140452916,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140452923,"alleles":["CACACACA","CACACA"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794367734","clinical_significance":[]},{"id":"rs1794367808","seq_region_name":"7","clinical_significance":[],"start":140452918,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140452918,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1794367881","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452919,"source":"dbSNP","strand":1,"feature_type":"variation","end":140452919,"alleles":["A","AA"]},{"clinical_significance":[],"id":"rs1193177854","seq_region_name":"7","end":140452920,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140452920,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794367994","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452921,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140452921},{"feature_type":"variation","strand":1,"end":140452922,"alleles":["C","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452922,"clinical_significance":[],"seq_region_name":"7","id":"rs11760895"},{"clinical_significance":[],"id":"rs1246500527","seq_region_name":"7","end":140452932,"alleles":["AAA","AA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140452930,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1480996353","clinical_significance":[],"start":140452932,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140452932,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1794368512","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452933,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140452933},{"seq_region_name":"7","id":"rs1794368579","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452934,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140452934},{"clinical_significance":[],"seq_region_name":"7","id":"rs1466691632","source":"dbSNP","start":140452936,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140452936,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1794368713","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140452937,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452937,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs563846418","end":140452938,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140452938,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452945,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140452945,"clinical_significance":[],"seq_region_name":"7","id":"rs1794368867"},{"id":"rs934925240","seq_region_name":"7","clinical_significance":[],"end":140452946,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140452946,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452947,"feature_type":"variation","strand":1,"end":140452947,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs146921220"},{"clinical_significance":[],"seq_region_name":"7","id":"rs995198378","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452949,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140452949},{"end":140452952,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140452952,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1794369204","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1026198107","feature_type":"variation","strand":1,"end":140452953,"alleles":["C","A","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452953},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140452954,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452954,"clinical_significance":[],"seq_region_name":"7","id":"rs886443438"},{"seq_region_name":"7","id":"rs895474288","clinical_significance":[],"alleles":["G","A"],"end":140452955,"strand":1,"feature_type":"variation","start":140452955,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"alleles":["G","-"],"end":140452955,"strand":1,"feature_type":"variation","start":140452955,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1342536224","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1435714712","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452957,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140452957},{"seq_region_name":"7","id":"rs773562127","clinical_significance":[],"start":140452960,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140452960,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1019001610","clinical_significance":[],"start":140452965,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140452965,"alleles":["C","A","G","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs549629754","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452966,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140452966},{"clinical_significance":[],"seq_region_name":"7","id":"rs865798613","source":"dbSNP","start":140452969,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140452969,"alleles":["C","G","T"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["G","A","C","T"],"end":140452970,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452970,"clinical_significance":[],"seq_region_name":"7","id":"rs1044444207"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452972,"source":"dbSNP","strand":1,"feature_type":"variation","end":140452975,"alleles":["AGAG","AG"],"seq_region_name":"7","id":"rs1794370260","clinical_significance":[]},{"source":"dbSNP","start":140452979,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140452979,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1451851834"},{"clinical_significance":[],"id":"rs1246767507","seq_region_name":"7","alleles":["A","C"],"end":140452982,"feature_type":"variation","strand":1,"source":"dbSNP","start":140452982,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1794370488","seq_region_name":"7","end":140452984,"alleles":["AAA","AAAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140452982,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1474044421","seq_region_name":"7","alleles":["C","T"],"end":140452991,"feature_type":"variation","strand":1,"source":"dbSNP","start":140452991,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs761204223","clinical_significance":[],"strand":1,"feature_type":"variation","end":140452996,"alleles":["CATCAT","CAT"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140452991,"source":"dbSNP"},{"clinical_significance":[],"id":"rs561743819","seq_region_name":"7","feature_type":"variation","strand":1,"end":140452995,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140452995},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140453001,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453001,"clinical_significance":[],"id":"rs763024447","seq_region_name":"7"},{"seq_region_name":"7","id":"rs2130227882","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140453003,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140453003},{"clinical_significance":[],"seq_region_name":"7","id":"rs968177604","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140453004,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453004},{"end":140453005,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140453005,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs978755918","seq_region_name":"7","clinical_significance":[]},{"end":140453008,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140453008,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1440398892","clinical_significance":[]},{"source":"dbSNP","start":140453009,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140453009,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794371203"},{"start":140453010,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140453010,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs529043537","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140453015,"source":"dbSNP","strand":1,"feature_type":"variation","end":140453015,"alleles":["C","G","T"],"id":"rs766644923","seq_region_name":"7","clinical_significance":[]},{"start":140453022,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140453022,"strand":1,"feature_type":"variation","id":"rs934337027","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1344085348","clinical_significance":[],"start":140453023,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","C"],"end":140453023,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["AACAGCTCATTACACAGAACAGC","AACAGC"],"end":140453046,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453024,"clinical_significance":[],"seq_region_name":"7","id":"rs1295250807"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453030,"feature_type":"variation","strand":1,"end":140453030,"alleles":["T","TT"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794371589"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140453032,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","T"],"end":140453032,"seq_region_name":"7","id":"rs1794371670","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs528717063","feature_type":"variation","strand":1,"end":140453034,"alleles":["T","C"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453034},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794373682","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453036,"feature_type":"variation","strand":1,"end":140453036,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1794373740","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140453038,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453038,"source":"dbSNP"},{"end":140453039,"alleles":["A","-"],"strand":1,"feature_type":"variation","start":140453039,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs1369833926","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1415198219","end":140453039,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140453039,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"id":"rs896962134","seq_region_name":"7","clinical_significance":[],"start":140453040,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["G","C"],"end":140453040,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1314541157","clinical_significance":[],"strand":1,"feature_type":"variation","end":140453044,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453044,"source":"dbSNP"},{"clinical_significance":[],"id":"rs998532171","seq_region_name":"7","feature_type":"variation","strand":1,"end":140453045,"alleles":["G","A","C"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453045},{"clinical_significance":[],"seq_region_name":"7","id":"rs1226883276","feature_type":"variation","strand":1,"end":140453059,"alleles":["TTTTTTTTT","TTTTTTTT","TTTTTTTTTT"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453051},{"clinical_significance":[],"id":"rs1431970301","seq_region_name":"7","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453052,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140453052},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794374141","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453054,"feature_type":"variation","strand":1,"end":140453054,"alleles":["T","C"]},{"feature_type":"variation","strand":1,"end":140453063,"alleles":["TTAATT","TT"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453058,"clinical_significance":[],"id":"rs948491767","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453059,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140453059,"id":"rs547406707","seq_region_name":"7","clinical_significance":[]},{"end":140453061,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140453061,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1445843187"},{"source":"dbSNP","start":140453070,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140453070,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794374262"},{"seq_region_name":"7","id":"rs899007778","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453073,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140453073},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453073,"feature_type":"variation","strand":1,"end":140453075,"alleles":["GGG","GGGG"],"clinical_significance":[],"id":"rs35415979","seq_region_name":"7"},{"id":"rs1794374464","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140453079,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453079,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794374543","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453080,"feature_type":"variation","strand":1,"alleles":["GTG","GTGTG"],"end":140453082},{"end":140453083,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140453083,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794374633"},{"feature_type":"variation","strand":1,"end":140453086,"alleles":["C","T"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453086,"clinical_significance":[],"seq_region_name":"7","id":"rs1183151718"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794374750","alleles":["A","G"],"end":140453092,"feature_type":"variation","strand":1,"source":"dbSNP","start":140453092,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140453096,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453096,"source":"dbSNP","id":"rs565629702","seq_region_name":"7","clinical_significance":[]},{"start":140453102,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["T","TT"],"end":140453102,"strand":1,"feature_type":"variation","id":"rs34717400","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs930455656","source":"dbSNP","start":140453110,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["ACA","A"],"end":140453112,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs867688942","seq_region_name":"7","source":"dbSNP","start":140453112,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["A","G","T"],"end":140453112,"feature_type":"variation","strand":1},{"id":"rs1236495619","seq_region_name":"7","clinical_significance":[],"alleles":["AGAGA","AGAGAGA"],"end":140453116,"strand":1,"feature_type":"variation","start":140453112,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453113,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140453113,"clinical_significance":[],"seq_region_name":"7","id":"rs1273143563"},{"seq_region_name":"7","id":"rs1483043972","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140453115,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453115,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140453118,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453118,"source":"dbSNP","id":"rs1048128359","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140453121,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140453121,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794375441"},{"end":140453125,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140453125,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1794375520","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140453126,"alleles":["C","T"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453126,"clinical_significance":[],"seq_region_name":"7","id":"rs2130228488"},{"start":140453129,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["TTATTT","TT"],"end":140453134,"strand":1,"feature_type":"variation","id":"rs1794375614","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1204342663","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453130,"source":"dbSNP","strand":1,"feature_type":"variation","end":140453130,"alleles":["T","G"]},{"source":"dbSNP","start":140453131,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140453131,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1794375787","seq_region_name":"7"},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453132,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140453132,"clinical_significance":[],"seq_region_name":"7","id":"rs1794375845"},{"end":140453134,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140453134,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794375930"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794375976","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140453135,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453135},{"start":140453136,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["T","C"],"end":140453136,"strand":1,"feature_type":"variation","id":"rs1314912853","seq_region_name":"7","clinical_significance":[]},{"end":140453141,"alleles":["TTTTTT","TTT","TTTTTTT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140453136,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1322315832"},{"clinical_significance":[],"id":"rs1794376162","seq_region_name":"7","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453140,"feature_type":"variation","strand":1,"end":140453140,"alleles":["T","C"]},{"feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140453145,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453145,"clinical_significance":[],"seq_region_name":"7","id":"rs539065725"},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453145,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AAA","AAAA"],"end":140453147,"seq_region_name":"7","id":"rs1226718781","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794376367","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140453148,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453148,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1794376475","seq_region_name":"7","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453149,"feature_type":"variation","strand":1,"end":140453149,"alleles":["T","G"]},{"seq_region_name":"7","id":"rs1009219346","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453150,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140453150},{"clinical_significance":[],"seq_region_name":"7","id":"rs1018927672","alleles":["A","G"],"end":140453151,"feature_type":"variation","strand":1,"source":"dbSNP","start":140453151,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"end":140453157,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140453157,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs1794377626","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140453162,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453162,"source":"dbSNP","seq_region_name":"7","id":"rs14493","clinical_significance":[]},{"start":140453163,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140453163,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs764772826","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453164,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140453164,"seq_region_name":"7","id":"rs1794377819","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140453165,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453165,"clinical_significance":[],"seq_region_name":"7","id":"rs551625797"},{"end":140453166,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140453166,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs900506614","seq_region_name":"7"},{"seq_region_name":"7","id":"rs776062566","clinical_significance":[],"end":140453170,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140453170,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"alleles":["G","A"],"end":140453171,"feature_type":"variation","strand":1,"source":"dbSNP","start":140453171,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794377989"},{"clinical_significance":[],"seq_region_name":"7","id":"rs34122062","feature_type":"variation","strand":1,"end":140453172,"alleles":["-","C"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453173},{"id":"rs2130228854","seq_region_name":"7","clinical_significance":[],"start":140453176,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140453176,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585457067","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453180,"feature_type":"variation","strand":1,"end":140453180,"alleles":["G","C"]},{"seq_region_name":"7","id":"rs1352164724","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453181,"source":"dbSNP","strand":1,"feature_type":"variation","end":140453181,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1163330034","alleles":["T","C"],"end":140453184,"feature_type":"variation","strand":1,"source":"dbSNP","start":140453184,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"end":140453185,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140453185,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1421492947"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140453187,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453187,"clinical_significance":[],"seq_region_name":"7","id":"rs1412463434"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1182371163","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453188,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140453188},{"source":"dbSNP","start":140453195,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140453195,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794378363"},{"seq_region_name":"7","id":"rs1022301252","clinical_significance":[],"strand":1,"feature_type":"variation","end":140453197,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453197,"source":"dbSNP"},{"id":"rs1585457113","seq_region_name":"7","clinical_significance":[],"start":140453199,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["G","C"],"end":140453199,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140453200,"alleles":["G","A"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453200,"clinical_significance":[],"id":"rs968623590","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1801678","clinical_significance":[],"end":140453201,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140453201,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"seq_region_name":"7","id":"rs1794378638","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140453202,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453202,"source":"dbSNP"},{"seq_region_name":"7","id":"rs2130229018","clinical_significance":[],"alleles":["C","T"],"end":140453203,"strand":1,"feature_type":"variation","start":140453203,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140453205,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453205,"source":"dbSNP","seq_region_name":"7","id":"rs1181242280","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794378736","source":"dbSNP","start":140453206,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140453206,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1794378784","clinical_significance":[],"strand":1,"feature_type":"variation","end":140453208,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453208,"source":"dbSNP"},{"clinical_significance":[],"id":"rs2130229065","seq_region_name":"7","source":"dbSNP","start":140453209,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140453209,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1167647470","source":"dbSNP","start":140453210,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140453210,"alleles":["G","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1267100673","clinical_significance":[],"strand":1,"feature_type":"variation","end":140453212,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453212,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1388986368","seq_region_name":"7","end":140453226,"alleles":["TATTTTCAGGAAA","TATTTTCAGGAAATATTTTCAGGAAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140453214,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"alleles":["T","C"],"end":140453216,"feature_type":"variation","strand":1,"source":"dbSNP","start":140453216,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs569868310"},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453217,"source":"dbSNP","strand":1,"feature_type":"variation","end":140453217,"alleles":["T","G"],"id":"rs1794379082","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794379129","clinical_significance":[],"start":140453219,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140453219,"alleles":["T","G"],"strand":1,"feature_type":"variation"},{"start":140453223,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140453223,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794379181","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794379248","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453224,"feature_type":"variation","strand":1,"end":140453224,"alleles":["A","C"]},{"clinical_significance":[],"id":"rs1321135394","seq_region_name":"7","source":"dbSNP","start":140453224,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140453226,"alleles":["AAA","A"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140453229,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453229,"clinical_significance":[],"seq_region_name":"7","id":"rs1268923049"},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453232,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140453232,"seq_region_name":"7","id":"rs1794379637","clinical_significance":[]},{"end":140453234,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140453234,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794379689"},{"seq_region_name":"7","id":"rs1794379731","clinical_significance":[],"strand":1,"feature_type":"variation","end":140453241,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453241,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794379795","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140453242,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453242},{"id":"rs2130229261","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453244,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AAGGTACAATTTCCAA","AA"],"end":140453259},{"clinical_significance":[],"seq_region_name":"7","id":"rs536834489","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140453248,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453248},{"end":140453250,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140453250,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs555172057"},{"start":140453254,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["T","C"],"end":140453254,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1175432008","clinical_significance":[]},{"id":"rs1288080846","seq_region_name":"7","clinical_significance":[],"alleles":["C","A"],"end":140453261,"strand":1,"feature_type":"variation","start":140453261,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140453263,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453263,"source":"dbSNP","seq_region_name":"7","id":"rs1387672908","clinical_significance":[]},{"alleles":["G","T"],"end":140453265,"strand":1,"feature_type":"variation","start":140453265,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs759194824","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs961016595","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453268,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140453268},{"seq_region_name":"7","id":"rs992408950","clinical_significance":[],"end":140453270,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140453270,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs916953130","feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140453274,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453274},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453278,"source":"dbSNP","strand":1,"feature_type":"variation","end":140453279,"alleles":["AA","A"],"seq_region_name":"7","id":"rs1159329655","clinical_significance":[]},{"id":"rs573795558","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140453280,"strand":1,"feature_type":"variation","start":140453280,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs948335643","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453285,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140453285},{"seq_region_name":"7","id":"rs1433504251","clinical_significance":[],"end":140453288,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140453288,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"id":"rs534834861","seq_region_name":"7","clinical_significance":[],"alleles":["A","C"],"end":140453289,"strand":1,"feature_type":"variation","start":140453289,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"clinical_significance":[],"id":"rs1446941696","seq_region_name":"7","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453293,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140453293},{"end":140453295,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140453295,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1302487953","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794380703","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453303,"feature_type":"variation","strand":1,"end":140453303,"alleles":["A","G"]},{"alleles":["A","G"],"end":140453310,"feature_type":"variation","strand":1,"source":"dbSNP","start":140453310,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1488151071","seq_region_name":"7"},{"alleles":["C","G"],"end":140453313,"strand":1,"feature_type":"variation","start":140453313,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs1248699785","clinical_significance":[]},{"start":140453314,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140453314,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794380794","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794380856","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140453319,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453319},{"clinical_significance":[],"seq_region_name":"7","id":"rs1362873349","source":"dbSNP","start":140453322,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140453322,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs553203504","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140453323,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453323,"source":"dbSNP"},{"alleles":["G","A"],"end":140453327,"strand":1,"feature_type":"variation","start":140453327,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs1794380994","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140453334,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453334,"source":"dbSNP","id":"rs1234261234","seq_region_name":"7","clinical_significance":[]},{"id":"rs1794381101","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140453335,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453335,"source":"dbSNP"},{"end":140453340,"alleles":["TT","T"],"strand":1,"feature_type":"variation","start":140453339,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs1384017792","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453342,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140453342,"seq_region_name":"7","id":"rs1314244587","clinical_significance":[]},{"source":"dbSNP","start":140453345,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140453345,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1318605219","seq_region_name":"7"},{"end":140453346,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140453346,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs979851604"},{"clinical_significance":[],"id":"rs1794381333","seq_region_name":"7","source":"dbSNP","start":140453348,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140453348,"feature_type":"variation","strand":1},{"alleles":["T","C"],"end":140453356,"strand":1,"feature_type":"variation","start":140453356,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","id":"rs1794381390","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140453358,"alleles":["A","AA"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453358,"clinical_significance":[],"seq_region_name":"7","id":"rs1386690074"},{"alleles":["CTCC","-"],"end":140453362,"feature_type":"variation","strand":1,"source":"dbSNP","start":140453359,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1295551017","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1366618830","end":140453363,"alleles":["TCCA","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140453360,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["C","CC"],"end":140453364,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453364,"clinical_significance":[],"seq_region_name":"7","id":"rs1341541194"},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453367,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140453367,"seq_region_name":"7","id":"rs1794381932","clinical_significance":[]},{"clinical_significance":[],"id":"rs1364608980","seq_region_name":"7","source":"dbSNP","start":140453369,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140453369,"feature_type":"variation","strand":1},{"start":140453370,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140453370,"alleles":["T","C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794382024","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs753822740","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140453371,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453371},{"end":140453376,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140453376,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1436590307","seq_region_name":"7"},{"seq_region_name":"7","id":"rs764867145","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140453379,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453379,"source":"dbSNP"},{"id":"rs2130229909","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140453381,"strand":1,"feature_type":"variation","start":140453381,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"strand":1,"feature_type":"variation","end":140453384,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453384,"source":"dbSNP","id":"rs1157570495","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794385699","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["AGAG","AG"],"end":140453388,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453385,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140453386,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453386,"clinical_significance":[],"seq_region_name":"7","id":"rs577938574"},{"seq_region_name":"7","id":"rs189288235","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453392,"source":"dbSNP","strand":1,"feature_type":"variation","end":140453392,"alleles":["T","G"]},{"id":"rs1379143373","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453393,"source":"dbSNP","strand":1,"feature_type":"variation","end":140453393,"alleles":["G","C"]},{"start":140453394,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140453395,"alleles":["AA","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1310817767","clinical_significance":[]},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453396,"feature_type":"variation","strand":1,"end":140453396,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1173755532"},{"seq_region_name":"7","id":"rs1047588832","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453399,"source":"dbSNP","strand":1,"feature_type":"variation","end":140453399,"alleles":["C","G","T"]},{"end":140453399,"alleles":["C","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140453399,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1209809208"},{"clinical_significance":[],"seq_region_name":"7","id":"rs757265814","alleles":["G","A"],"end":140453400,"feature_type":"variation","strand":1,"source":"dbSNP","start":140453400,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"end":140453407,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140453407,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794386172"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794386225","feature_type":"variation","strand":1,"end":140453409,"alleles":["C","T"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453409},{"seq_region_name":"7","id":"rs2130230066","clinical_significance":[],"strand":1,"feature_type":"variation","end":140453411,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453411,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453412,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140453412,"seq_region_name":"7","id":"rs1190464290","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794386316","alleles":["-","C"],"end":140453412,"feature_type":"variation","strand":1,"source":"dbSNP","start":140453413,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140453422,"alleles":["G","A"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453422,"clinical_significance":[],"seq_region_name":"7","id":"rs1794386358"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1486672632","alleles":["T","C"],"end":140453425,"feature_type":"variation","strand":1,"source":"dbSNP","start":140453425,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"id":"rs1261139393","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140453426,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453426,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs907684794","alleles":["G","A"],"end":140453427,"feature_type":"variation","strand":1,"source":"dbSNP","start":140453427,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140453428,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140453428,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794386528"},{"id":"rs1484392245","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140453431,"strand":1,"feature_type":"variation","start":140453431,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1186242174","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453432,"feature_type":"variation","strand":1,"end":140453432,"alleles":["A","T"]},{"id":"rs200061500","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","G"],"end":140453435,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453435,"source":"dbSNP"},{"end":140453439,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140453439,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs1246947871","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453441,"source":"dbSNP","strand":1,"feature_type":"variation","end":140453441,"alleles":["C","T"],"seq_region_name":"7","id":"rs1343350333","clinical_significance":[]},{"alleles":["CACAAAAACAAACACAAAAAC","CACAAAAAC"],"end":140453463,"feature_type":"variation","strand":1,"source":"dbSNP","start":140453443,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1300383705"},{"seq_region_name":"7","id":"rs1794388605","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453451,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140453451},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453457,"source":"dbSNP","strand":1,"feature_type":"variation","end":140453457,"alleles":["C","A"],"id":"rs1794388679","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1226852797","clinical_significance":[],"strand":1,"feature_type":"variation","end":140453458,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453458,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1794388813","clinical_significance":[],"alleles":["A","G"],"end":140453462,"strand":1,"feature_type":"variation","start":140453462,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"strand":1,"feature_type":"variation","end":140453465,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453465,"source":"dbSNP","id":"rs563991525","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs944676542","clinical_significance":[],"start":140453466,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["G","A"],"end":140453466,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1396231496","feature_type":"variation","strand":1,"alleles":["ACAACAA","ACAA"],"end":140453473,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453467},{"alleles":["G","A"],"end":140453477,"feature_type":"variation","strand":1,"source":"dbSNP","start":140453477,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1040257292","seq_region_name":"7"},{"id":"rs2130230327","seq_region_name":"7","clinical_significance":[],"start":140453482,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["AA","AAA"],"end":140453483,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794389073","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453484,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140453484},{"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140453485,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453485,"clinical_significance":[],"id":"rs1794389124","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453487,"source":"dbSNP","strand":1,"feature_type":"variation","end":140453487,"alleles":["A","G"],"seq_region_name":"7","id":"rs1794389171","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794389212","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453488,"feature_type":"variation","strand":1,"end":140453488,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1300749734","feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140453491,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453491},{"clinical_significance":[],"id":"rs1563084191","seq_region_name":"7","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453492,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140453492},{"id":"rs778794996","seq_region_name":"7","clinical_significance":[],"end":140453496,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140453496,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"strand":1,"feature_type":"variation","end":140453497,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453497,"source":"dbSNP","id":"rs1794389395","seq_region_name":"7","clinical_significance":[]},{"id":"rs1794389432","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140453498,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453498,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140453504,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453504,"clinical_significance":[],"seq_region_name":"7","id":"rs1370957985"},{"feature_type":"variation","strand":1,"end":140453506,"alleles":["A","C"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453506,"clinical_significance":[],"seq_region_name":"7","id":"rs1794389546"},{"seq_region_name":"7","id":"rs17620927","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140453511,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453511,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1639393116","clinical_significance":[],"start":140453513,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140453513,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"id":"rs1794389672","seq_region_name":"7","clinical_significance":[],"start":140453514,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140453514,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1447657679","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453515,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140453515},{"end":140453517,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140453517,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1372567914"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794389813","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140453518,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453518},{"start":140453520,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140453520,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs575873701","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1425746480","end":140453524,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140453524,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1413730199","seq_region_name":"7","feature_type":"variation","strand":1,"end":140453525,"alleles":["G","C"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453525},{"seq_region_name":"7","id":"rs1210461353","clinical_significance":[],"start":140453526,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["C","A"],"end":140453526,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140453527,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453527,"source":"dbSNP","seq_region_name":"7","id":"rs1794390046","clinical_significance":[]},{"end":140453529,"alleles":["AG","AGGAG"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140453528,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794390295"},{"end":140453532,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140453532,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","id":"rs1483553303","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140453533,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453533,"source":"dbSNP","id":"rs752549811","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","G"],"end":140453535,"feature_type":"variation","strand":1,"source":"dbSNP","start":140453535,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1043806995"},{"clinical_significance":[],"id":"rs1794390496","seq_region_name":"7","feature_type":"variation","strand":1,"end":140453538,"alleles":["A","G"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453538},{"seq_region_name":"7","id":"rs1342138685","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140453540,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453540,"source":"dbSNP"},{"seq_region_name":"7","id":"rs903906877","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453543,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140453543},{"seq_region_name":"7","id":"rs1794390621","clinical_significance":[],"end":140453545,"alleles":["AAA","AAAA"],"strand":1,"feature_type":"variation","start":140453543,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"end":140453545,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140453545,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1000004675","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1794390704","clinical_significance":[],"end":140453546,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140453546,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"source":"dbSNP","start":140453552,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["T","-"],"end":140453552,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1341769359"},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453552,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140453552,"clinical_significance":[],"seq_region_name":"7","id":"rs1794390787"},{"feature_type":"variation","strand":1,"end":140453557,"alleles":["A","T"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453557,"clinical_significance":[],"id":"rs1794390891","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1794390929","seq_region_name":"7","feature_type":"variation","strand":1,"end":140453557,"alleles":["A","AA"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453557},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453559,"feature_type":"variation","strand":1,"end":140453559,"alleles":["C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs147568103"},{"feature_type":"variation","strand":1,"end":140453563,"alleles":["G","C"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453563,"clinical_significance":[],"seq_region_name":"7","id":"rs1413797768"},{"seq_region_name":"7","id":"rs1794391064","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453569,"source":"dbSNP","strand":1,"feature_type":"variation","end":140453569,"alleles":["G","C"]},{"end":140453576,"alleles":["TGTGT","TGT"],"strand":1,"feature_type":"variation","start":140453572,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","id":"rs961152267","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453574,"feature_type":"variation","strand":1,"end":140453574,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1318772197"},{"start":140453579,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140453579,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","id":"rs1364566580","seq_region_name":"7","clinical_significance":[]},{"start":140453582,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["T","C"],"end":140453582,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1297945935","clinical_significance":[]},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453584,"feature_type":"variation","strand":1,"end":140453584,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794391277"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1163799283","alleles":["G","C"],"end":140453586,"feature_type":"variation","strand":1,"source":"dbSNP","start":140453586,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"start":140453590,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140453590,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130230941","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140453591,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453591,"source":"dbSNP","seq_region_name":"7","id":"rs1459460341","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140453592,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453592,"source":"dbSNP","id":"rs1366811678","seq_region_name":"7","clinical_significance":[]},{"end":140453593,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140453593,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs1441645368","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["AGGTAG","AG"],"end":140453599,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453594,"clinical_significance":[],"id":"rs1794391527","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1306313326","clinical_significance":[],"alleles":["G","T"],"end":140453595,"strand":1,"feature_type":"variation","start":140453595,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"start":140453599,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["G","T"],"end":140453599,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794391640","clinical_significance":[]},{"source":"dbSNP","start":140453600,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140453600,"alleles":["T","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1794391692","seq_region_name":"7"},{"alleles":["C","G"],"end":140453606,"feature_type":"variation","strand":1,"source":"dbSNP","start":140453606,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1013853688","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1366052293","seq_region_name":"7","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453612,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140453612},{"end":140453613,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140453613,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794391829"},{"alleles":["G","A"],"end":140453614,"strand":1,"feature_type":"variation","start":140453614,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","id":"rs1794391874","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453619,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140453619,"clinical_significance":[],"id":"rs1180524232","seq_region_name":"7"},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453622,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140453622,"clinical_significance":[],"seq_region_name":"7","id":"rs762711349"},{"clinical_significance":[],"seq_region_name":"7","id":"rs142013775","alleles":["T","C"],"end":140453624,"feature_type":"variation","strand":1,"source":"dbSNP","start":140453624,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794393009","feature_type":"variation","strand":1,"end":140453626,"alleles":["T","C","G"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453626},{"strand":1,"feature_type":"variation","end":140453631,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453631,"source":"dbSNP","id":"rs528705971","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794393113","clinical_significance":[],"alleles":["T","C"],"end":140453632,"strand":1,"feature_type":"variation","start":140453632,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453636,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140453636,"clinical_significance":[],"id":"rs541080082","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1270802767","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453637,"source":"dbSNP","strand":1,"feature_type":"variation","end":140453637,"alleles":["A","G"]},{"id":"rs920243249","seq_region_name":"7","clinical_significance":[],"start":140453638,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["T","C"],"end":140453638,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794393314","feature_type":"variation","strand":1,"end":140453639,"alleles":["A","G"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453639},{"strand":1,"feature_type":"variation","alleles":["G","C","T"],"end":140453640,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453640,"source":"dbSNP","id":"rs1350783602","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","A"],"end":140453642,"feature_type":"variation","strand":1,"source":"dbSNP","start":140453642,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1407720560"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794393466","source":"dbSNP","start":140453645,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["AGCTAGC","AGCTAGCTAGC"],"end":140453651,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs951854765","clinical_significance":[],"start":140453658,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140453658,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs983606482","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453661,"feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140453661},{"clinical_significance":[],"id":"rs1563084298","seq_region_name":"7","source":"dbSNP","start":140453667,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140453667,"alleles":["A","G"],"feature_type":"variation","strand":1},{"start":140453673,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["A","G","T"],"end":140453673,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1209513977","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1388449970","alleles":["A","G"],"end":140453674,"feature_type":"variation","strand":1,"source":"dbSNP","start":140453674,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1585457785","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453677,"source":"dbSNP","strand":1,"feature_type":"variation","end":140453677,"alleles":["T","C","G"]},{"start":140453680,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["T","TTT"],"end":140453680,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794393815","clinical_significance":[]},{"end":140453682,"alleles":["GC","GCGC"],"strand":1,"feature_type":"variation","start":140453681,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","id":"rs1794393868","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140453682,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453682,"source":"dbSNP","seq_region_name":"7","id":"rs192759214","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs112549820","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453683,"feature_type":"variation","strand":1,"end":140453683,"alleles":["T","C"]},{"start":140453688,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["C","T"],"end":140453688,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794394031","clinical_significance":[]},{"alleles":["T","A"],"end":140453690,"strand":1,"feature_type":"variation","start":140453690,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","id":"rs1457938983","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140453692,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453692,"source":"dbSNP","seq_region_name":"7","id":"rs1414418203","clinical_significance":[]},{"clinical_significance":[],"id":"rs1794394210","seq_region_name":"7","feature_type":"variation","strand":1,"end":140453695,"alleles":["G","T"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453695},{"clinical_significance":[],"id":"rs1040268703","seq_region_name":"7","source":"dbSNP","start":140453697,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140453697,"alleles":["T","C"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453702,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140453702,"seq_region_name":"7","id":"rs1794394328","clinical_significance":[]},{"start":140453708,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["C","T"],"end":140453708,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1468541936","clinical_significance":[]},{"seq_region_name":"7","id":"rs1682598309","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453709,"source":"dbSNP","strand":1,"feature_type":"variation","end":140453709,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs551126552","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453712,"source":"dbSNP","strand":1,"feature_type":"variation","end":140453712,"alleles":["A","C"]},{"end":140453719,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140453719,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1794394493","seq_region_name":"7"},{"end":140453721,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140453721,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs1201646355","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794394592","source":"dbSNP","start":140453731,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140453731,"feature_type":"variation","strand":1},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453732,"feature_type":"variation","strand":1,"end":140453732,"alleles":["G","A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs931995499"},{"seq_region_name":"7","id":"rs1194916544","clinical_significance":[],"alleles":["TTTTT","TTTT"],"end":140453738,"strand":1,"feature_type":"variation","start":140453734,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1212563796","alleles":["T","C"],"end":140453737,"feature_type":"variation","strand":1,"source":"dbSNP","start":140453737,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453738,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140453738,"clinical_significance":[],"seq_region_name":"7","id":"rs1244932987"},{"alleles":["C","G"],"end":140453739,"feature_type":"variation","strand":1,"source":"dbSNP","start":140453739,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794394874"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794394925","feature_type":"variation","strand":1,"alleles":["-","TTTTTCTACTAAGGTTTTTCTA"],"end":140453747,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453748},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130231673","end":140453750,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140453750,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"end":140453757,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140453757,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","id":"rs1794394974","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794395021","clinical_significance":[],"end":140453759,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140453759,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1269569812","feature_type":"variation","strand":1,"end":140453760,"alleles":["C","T"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453760},{"alleles":["T","A"],"end":140453762,"feature_type":"variation","strand":1,"source":"dbSNP","start":140453762,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1043734261"},{"alleles":["C","A"],"end":140453763,"strand":1,"feature_type":"variation","start":140453763,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs1563084342","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1477685024","source":"dbSNP","start":140453764,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140453764,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1177707253","seq_region_name":"7","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453765,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140453765},{"id":"rs1438504922","seq_region_name":"7","clinical_significance":[],"end":140453768,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140453768,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs569911355","feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140453770,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453770},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453771,"source":"dbSNP","strand":1,"feature_type":"variation","end":140453771,"alleles":["G","C"],"seq_region_name":"7","id":"rs2130231836","clinical_significance":[]},{"id":"rs2130231851","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140453772,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453772,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs530764176","alleles":["G","A"],"end":140453775,"feature_type":"variation","strand":1,"source":"dbSNP","start":140453775,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1794395466","clinical_significance":[],"strand":1,"feature_type":"variation","end":140453776,"alleles":["A","AA"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453776,"source":"dbSNP"},{"source":"dbSNP","start":140453778,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140453778,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1325176248"},{"source":"dbSNP","start":140453780,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140453780,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs999650144"},{"seq_region_name":"7","id":"rs1794395601","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["CACACACCCACACAC","CACACAC"],"end":140453800,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453786,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140453791,"alleles":["ACACA","-"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453787,"clinical_significance":[],"seq_region_name":"7","id":"rs757166269"},{"clinical_significance":[],"id":"rs1794395699","seq_region_name":"7","source":"dbSNP","start":140453790,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140453790,"feature_type":"variation","strand":1},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453793,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140453793,"clinical_significance":[],"seq_region_name":"7","id":"rs1052914890"},{"start":140453794,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140453800,"alleles":["CACACAC","CACAC"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1400417626","clinical_significance":[]},{"end":140453798,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140453798,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130232009"},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453802,"feature_type":"variation","strand":1,"end":140453802,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1426302195"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1388135893","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453804,"feature_type":"variation","strand":1,"end":140453804,"alleles":["C","A"]},{"source":"dbSNP","start":140453806,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140453806,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794395925"},{"end":140453809,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140453809,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1462054565","seq_region_name":"7"},{"start":140453813,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140453813,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794396019","clinical_significance":[]},{"alleles":["G","C"],"end":140453814,"strand":1,"feature_type":"variation","start":140453814,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs1794396079","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585457989","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453815,"feature_type":"variation","strand":1,"end":140453815,"alleles":["C","T"]},{"id":"rs1328067889","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140453820,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453820,"source":"dbSNP"},{"clinical_significance":[],"id":"rs896655717","seq_region_name":"7","end":140453822,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140453822,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"end":140453828,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140453828,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","id":"rs1794396309","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1794396356","seq_region_name":"7","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453835,"feature_type":"variation","strand":1,"end":140453835,"alleles":["A","C","T"]},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453836,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140453836,"seq_region_name":"7","id":"rs538954705","clinical_significance":[]},{"start":140453839,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["T","C"],"end":140453839,"strand":1,"feature_type":"variation","id":"rs1280630210","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","T"],"end":140453841,"strand":1,"feature_type":"variation","start":140453841,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs1794396516","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140453843,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453843,"source":"dbSNP","seq_region_name":"7","id":"rs1013739282","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1375999369","source":"dbSNP","start":140453844,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140453844,"feature_type":"variation","strand":1},{"alleles":["G","A"],"end":140453845,"feature_type":"variation","strand":1,"source":"dbSNP","start":140453845,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1464907536","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1226869596","feature_type":"variation","strand":1,"end":140453846,"alleles":["A","C"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453846},{"source":"dbSNP","start":140453854,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140453854,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1213203858","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["CTCTCT","CT"],"end":140453860,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453855,"source":"dbSNP","seq_region_name":"7","id":"rs1023908495","clinical_significance":[]},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453858,"feature_type":"variation","strand":1,"end":140453864,"alleles":["TCTATCT","TCT"],"clinical_significance":[],"id":"rs1335022316","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453859,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140453859,"seq_region_name":"7","id":"rs1794396875","clinical_significance":[]},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453860,"feature_type":"variation","strand":1,"end":140453860,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs969659286"},{"seq_region_name":"7","id":"rs1220702038","clinical_significance":[],"alleles":["TAT","T"],"end":140453862,"strand":1,"feature_type":"variation","start":140453860,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"end":140453861,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140453861,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1302514775"},{"clinical_significance":[],"id":"rs1794397069","seq_region_name":"7","end":140453869,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140453869,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["C","A","G","T"],"end":140453871,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453871,"clinical_significance":[],"id":"rs995742855","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1027364465","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140453872,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453872,"source":"dbSNP"},{"end":140453877,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140453877,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794397238"},{"clinical_significance":[],"id":"rs1585458141","seq_region_name":"7","alleles":["T","C"],"end":140453878,"feature_type":"variation","strand":1,"source":"dbSNP","start":140453878,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs548760771","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453880,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140453880},{"alleles":["T","G"],"end":140453882,"strand":1,"feature_type":"variation","start":140453882,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs1794397389","clinical_significance":[]},{"id":"rs1794397429","seq_region_name":"7","clinical_significance":[],"start":140453896,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["A","AA"],"end":140453896,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1794397466","clinical_significance":[],"start":140453897,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140453897,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs951791855","clinical_significance":[],"strand":1,"feature_type":"variation","end":140453899,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453899,"source":"dbSNP"},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453905,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140453905,"clinical_significance":[],"seq_region_name":"7","id":"rs567085312"},{"source":"dbSNP","start":140453905,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140453905,"alleles":["A","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794397605"},{"start":140453908,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140453913,"alleles":["AAAAAA","AAAAAAA","AAAAAAAA"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs60704749","clinical_significance":[]},{"clinical_significance":[],"id":"rs1585458193","seq_region_name":"7","alleles":["A","G"],"end":140453910,"feature_type":"variation","strand":1,"source":"dbSNP","start":140453910,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140453911,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453911,"source":"dbSNP","seq_region_name":"7","id":"rs1413071740","clinical_significance":[]},{"start":140453913,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["A","G"],"end":140453913,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794397814","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1215153855","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453914,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140453914},{"source":"dbSNP","start":140453915,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140453915,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1287213942"},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453922,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140453922,"seq_region_name":"7","id":"rs1794397950","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794397987","clinical_significance":[],"start":140453925,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140453925,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140453928,"alleles":["C","T"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453928,"clinical_significance":[],"id":"rs1794398031","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140453929,"alleles":["A","C","T"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453929,"source":"dbSNP","seq_region_name":"7","id":"rs1375232321","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140453930,"alleles":["C","A"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453930,"clinical_significance":[],"seq_region_name":"7","id":"rs1794398143"},{"start":140453931,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140453931,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs1450524704","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1451950363","seq_region_name":"7","alleles":["G","A"],"end":140453933,"feature_type":"variation","strand":1,"source":"dbSNP","start":140453933,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs150116435","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140453935,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453935},{"start":140453940,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["G","A"],"end":140453940,"strand":1,"feature_type":"variation","id":"rs1794398323","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1184306247","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140453941,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453941,"source":"dbSNP"},{"source":"dbSNP","start":140453946,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140453946,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794398403"},{"strand":1,"feature_type":"variation","end":140453947,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453947,"source":"dbSNP","seq_region_name":"7","id":"rs983227309","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794398502","feature_type":"variation","strand":1,"end":140453957,"alleles":["C","T"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453957},{"alleles":["G","A"],"end":140453960,"strand":1,"feature_type":"variation","start":140453960,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs768203250","clinical_significance":[]},{"id":"rs1794398603","seq_region_name":"7","clinical_significance":[],"start":140453961,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140453961,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140453964,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140453964,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs780742789"},{"seq_region_name":"7","id":"rs1484529737","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453972,"source":"dbSNP","strand":1,"feature_type":"variation","end":140453972,"alleles":["A","C"]},{"seq_region_name":"7","id":"rs1585458259","clinical_significance":[],"start":140453973,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140453973,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["AA","-"],"end":140453975,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453974,"clinical_significance":[],"seq_region_name":"7","id":"rs1794398787"},{"feature_type":"variation","strand":1,"end":140453975,"alleles":["A","G"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453975,"clinical_significance":[],"seq_region_name":"7","id":"rs1279429122"},{"seq_region_name":"7","id":"rs1181132310","clinical_significance":[],"start":140453975,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140453982,"alleles":["AGAGACCA","A"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453976,"source":"dbSNP","strand":1,"feature_type":"variation","end":140453976,"alleles":["G","A"],"seq_region_name":"7","id":"rs1794398965","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs755318734","source":"dbSNP","start":140453979,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140453979,"feature_type":"variation","strand":1},{"alleles":["C","A"],"end":140453980,"feature_type":"variation","strand":1,"source":"dbSNP","start":140453980,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs907575711"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794399123","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453982,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140453982},{"start":140453983,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["A","C"],"end":140453983,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1344299064","clinical_significance":[]},{"clinical_significance":[],"id":"rs1270937021","seq_region_name":"7","end":140453986,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140453986,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794399261","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140453992,"feature_type":"variation","strand":1,"end":140453992,"alleles":["A","C"]},{"start":140453995,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["AAGT","AAGTAAGT"],"end":140453998,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794399317","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140453997,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140453997,"source":"dbSNP","id":"rs1214024432","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140454002,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140454002,"source":"dbSNP","id":"rs748583587","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140454003,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140454003,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1286113823"},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454005,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140454005,"clinical_significance":[],"id":"rs1794399534","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1475683547","seq_region_name":"7","alleles":["G","C"],"end":140454006,"feature_type":"variation","strand":1,"source":"dbSNP","start":140454006,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454008,"feature_type":"variation","strand":1,"end":140454008,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794399625"},{"start":140454009,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140454011,"alleles":["GGG","GGGG"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794399671","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs529580769","end":140454010,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140454010,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454011,"feature_type":"variation","strand":1,"end":140454011,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794399779"},{"seq_region_name":"7","id":"rs1794399823","clinical_significance":[],"strand":1,"feature_type":"variation","end":140454018,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140454018,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140454019,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140454019,"seq_region_name":"7","id":"rs1309079781","clinical_significance":[]},{"end":140454023,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140454023,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794399913"},{"alleles":["G","A"],"end":140454024,"feature_type":"variation","strand":1,"source":"dbSNP","start":140454024,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1432145401"},{"clinical_significance":[],"seq_region_name":"7","id":"rs371344862","source":"dbSNP","start":140454025,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140454025,"alleles":["G","A","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs138583092","seq_region_name":"7","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454028,"feature_type":"variation","strand":1,"end":140454028,"alleles":["C","G","T"]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140454032,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454032,"clinical_significance":[],"seq_region_name":"7","id":"rs1794400127"},{"start":140454034,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140454034,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794400180","clinical_significance":[]},{"alleles":["AAAAA","AAAAAAA"],"end":140454039,"strand":1,"feature_type":"variation","start":140454035,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs1794400235","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140454037,"alleles":["A","G"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454037,"clinical_significance":[],"seq_region_name":"7","id":"rs2130233219"},{"start":140454038,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["A","C"],"end":140454038,"strand":1,"feature_type":"variation","id":"rs1794400283","seq_region_name":"7","clinical_significance":[]},{"alleles":["ACACA","ACA","ACACACA"],"end":140454043,"strand":1,"feature_type":"variation","start":140454039,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs1794400341","clinical_significance":[]},{"alleles":["C","T"],"end":140454042,"strand":1,"feature_type":"variation","start":140454042,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","id":"rs1794400413","seq_region_name":"7","clinical_significance":[]},{"id":"rs1408803384","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140454043,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140454043},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140454047,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140454047,"id":"rs1413894705","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs538999625","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140454048,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454048},{"clinical_significance":[],"seq_region_name":"7","id":"rs1474056573","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140454049,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454049},{"clinical_significance":[],"seq_region_name":"7","id":"rs1256519050","source":"dbSNP","start":140454055,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140454055,"alleles":["T","C"],"feature_type":"variation","strand":1},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454057,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140454057,"clinical_significance":[],"seq_region_name":"7","id":"rs1794400727"},{"seq_region_name":"7","id":"rs921754139","clinical_significance":[],"end":140454060,"alleles":["C","A","G"],"strand":1,"feature_type":"variation","start":140454060,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140454062,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454062,"clinical_significance":[],"seq_region_name":"7","id":"rs1483933368"},{"start":140454066,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["C","T"],"end":140454066,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794400887","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1249493017","feature_type":"variation","strand":1,"end":140454067,"alleles":["C","T"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454067},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794400988","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140454071,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454071},{"alleles":["T","C"],"end":140454075,"strand":1,"feature_type":"variation","start":140454075,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs931923285","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140454076,"source":"dbSNP","strand":1,"feature_type":"variation","end":140454076,"alleles":["C","T"],"seq_region_name":"7","id":"rs1794401091","clinical_significance":[]},{"start":140454085,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140454085,"alleles":["A","AA"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1322331073","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794401184","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140454087,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454087},{"start":140454088,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140454088,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1404777883","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140454094,"alleles":["GGGG","GGG"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454091,"clinical_significance":[],"seq_region_name":"7","id":"rs1292195380"},{"source":"dbSNP","start":140454092,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140454092,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1794401331","seq_region_name":"7"},{"seq_region_name":"7","id":"rs557122633","clinical_significance":[],"strand":1,"feature_type":"variation","end":140454093,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140454093,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1794401425","clinical_significance":[],"alleles":["G","A"],"end":140454094,"strand":1,"feature_type":"variation","start":140454094,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"id":"rs1334502099","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140454095,"source":"dbSNP","strand":1,"feature_type":"variation","end":140454095,"alleles":["C","T"]},{"start":140454097,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["G","C"],"end":140454097,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1356745497","clinical_significance":[]},{"clinical_significance":[],"id":"rs979755783","seq_region_name":"7","feature_type":"variation","strand":1,"end":140454099,"alleles":["G","A"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454099},{"end":140454101,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140454101,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794401640"},{"end":140454102,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140454102,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794401684"},{"id":"rs1794401754","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140454105,"strand":1,"feature_type":"variation","start":140454105,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140454109,"source":"dbSNP","strand":1,"feature_type":"variation","end":140454109,"alleles":["C","A"],"seq_region_name":"7","id":"rs1794401809","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794401842","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140454114,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TT","TTT"],"end":140454115},{"source":"dbSNP","start":140454117,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["GGTCCCTTCACCCATCACTCCTATTCTTGGACCCCAAAGCAGGGCCACTGCTTTTACTTTTGAACCTGGG","GGTCCCTTCACCCATCACTCCTATTCTTGGACCCCAAAGCAGGGCCACTGCTTTTACTTTTGAACCTGGGTCCCTTCACCCATCACTCCTATTCTTGGACCCCAAAGCAGGGCCACTGCTTTTACTTTTGAACCTGGG"],"end":140454186,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794401889"},{"source":"dbSNP","start":140454119,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140454119,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1371650908"},{"start":140454119,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["T","TT"],"end":140454119,"strand":1,"feature_type":"variation","id":"rs1794401959","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1298041930","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140454121,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454121},{"seq_region_name":"7","id":"rs1794402060","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140454128,"source":"dbSNP","strand":1,"feature_type":"variation","end":140454128,"alleles":["C","A"]},{"alleles":["A","C","G"],"end":140454130,"strand":1,"feature_type":"variation","start":140454130,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","id":"rs1408408902","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1307860188","seq_region_name":"7","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454131,"feature_type":"variation","strand":1,"end":140454131,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1166538485","clinical_significance":[],"alleles":["C","T"],"end":140454136,"strand":1,"feature_type":"variation","start":140454136,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"start":140454139,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["A","G"],"end":140454139,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1563084568","clinical_significance":[]},{"source":"dbSNP","start":140454146,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140454146,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130233719"},{"seq_region_name":"7","id":"rs925316153","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140454149,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140454149,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130233747","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454152,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140454152},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140454153,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140454153,"source":"dbSNP","seq_region_name":"7","id":"rs575997694","clinical_significance":[]},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454168,"feature_type":"variation","strand":1,"end":140454171,"alleles":["TTTT","TTT"],"clinical_significance":[],"id":"rs1234811485","seq_region_name":"7"},{"end":140454171,"alleles":["T","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140454171,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1159479204"},{"clinical_significance":[],"id":"rs551281749","seq_region_name":"7","feature_type":"variation","strand":1,"end":140454181,"alleles":["C","G","T"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454181},{"end":140454183,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140454183,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs1052549822","clinical_significance":[]},{"seq_region_name":"7","id":"rs1248150141","clinical_significance":[],"start":140454184,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["G","A"],"end":140454184,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140454185,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454185,"clinical_significance":[],"seq_region_name":"7","id":"rs1176544277"},{"clinical_significance":[],"seq_region_name":"7","id":"rs763404550","alleles":["G","A"],"end":140454187,"feature_type":"variation","strand":1,"source":"dbSNP","start":140454187,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"alleles":["C","A"],"end":140454189,"strand":1,"feature_type":"variation","start":140454189,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs11556753","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140454198,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140454198,"source":"dbSNP","seq_region_name":"7","id":"rs1794402786","clinical_significance":[]},{"seq_region_name":"7","id":"rs1488797798","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140454199,"source":"dbSNP","strand":1,"feature_type":"variation","end":140454199,"alleles":["A","T"]},{"id":"rs148884557","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140454200,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140454200,"source":"dbSNP"},{"alleles":["GTGTGTG","GTGTG"],"end":140454206,"feature_type":"variation","strand":1,"source":"dbSNP","start":140454200,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1282008637"},{"seq_region_name":"7","id":"rs1268947446","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140454201,"source":"dbSNP","strand":1,"feature_type":"variation","end":140454201,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1794403068","clinical_significance":[],"start":140454202,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["G","C"],"end":140454202,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1214606885","seq_region_name":"7","source":"dbSNP","start":140454204,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140454204,"alleles":["G","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1794403171","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140454205,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140454205},{"start":140454206,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140454206,"alleles":["G","T"],"strand":1,"feature_type":"variation","id":"rs1585458613","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1045283411","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140454208,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140454208},{"clinical_significance":[],"seq_region_name":"7","id":"rs772354941","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454211,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140454211},{"seq_region_name":"7","id":"rs1794403347","clinical_significance":[],"start":140454215,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140454215,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140454222,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454222,"clinical_significance":[],"seq_region_name":"7","id":"rs143595331"},{"end":140454223,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140454223,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs905360671"},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454224,"feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140454224,"clinical_significance":[],"seq_region_name":"7","id":"rs774609263"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794403596","end":140454225,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140454225,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1482062788","clinical_significance":[],"strand":1,"feature_type":"variation","end":140454229,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140454229,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140454231,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140454231,"source":"dbSNP","id":"rs1794405423","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585458670","clinical_significance":[],"start":140454238,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140454238,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585458674","source":"dbSNP","start":140454242,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140454242,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1393109912","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140454243,"source":"dbSNP","strand":1,"feature_type":"variation","end":140454243,"alleles":["A","T"]},{"source":"dbSNP","start":140454244,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140454244,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs778152751"},{"alleles":["G","A","T"],"end":140454245,"strand":1,"feature_type":"variation","start":140454245,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs1455081936","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140454246,"alleles":["C","A"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454246,"clinical_significance":[],"seq_region_name":"7","id":"rs1794405701"},{"start":140454247,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["A","G"],"end":140454247,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1004929867","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794405790","alleles":["C","A"],"end":140454249,"feature_type":"variation","strand":1,"source":"dbSNP","start":140454249,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794405842","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454256,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140454256},{"seq_region_name":"7","id":"rs1794405882","clinical_significance":[],"alleles":["C","T"],"end":140454257,"strand":1,"feature_type":"variation","start":140454257,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"strand":1,"feature_type":"variation","end":140454258,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140454258,"source":"dbSNP","seq_region_name":"7","id":"rs188718944","clinical_significance":[]},{"alleles":["T","C"],"end":140454260,"strand":1,"feature_type":"variation","start":140454260,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs1585458707","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794406043","clinical_significance":[],"alleles":["T","TCTT"],"end":140454260,"strand":1,"feature_type":"variation","start":140454260,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"seq_region_name":"7","id":"rs1433668176","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140454263,"source":"dbSNP","strand":1,"feature_type":"variation","end":140454269,"alleles":["CTGTCTG","CTG"]},{"seq_region_name":"7","id":"rs1396768302","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140454264,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140454264},{"seq_region_name":"7","id":"rs1191692412","clinical_significance":[],"start":140454268,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["T","TT"],"end":140454268,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1794406240","clinical_significance":[],"strand":1,"feature_type":"variation","end":140454271,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140454271,"source":"dbSNP"},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454272,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140454272,"clinical_significance":[],"seq_region_name":"7","id":"rs1486519710"},{"feature_type":"variation","strand":1,"end":140454275,"alleles":["-","G"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454276,"clinical_significance":[],"seq_region_name":"7","id":"rs1794406349"},{"id":"rs1794406397","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140454277,"source":"dbSNP","strand":1,"feature_type":"variation","end":140454277,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs747486049","clinical_significance":[],"start":140454279,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["T","C"],"end":140454279,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140454281,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140454281,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs540486305"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1485044499","source":"dbSNP","start":140454282,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140454282,"feature_type":"variation","strand":1},{"alleles":["TTACAAAAAACTAACTTT","T"],"end":140454302,"strand":1,"feature_type":"variation","start":140454285,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs1189889364","clinical_significance":[]},{"alleles":["A","T"],"end":140454287,"feature_type":"variation","strand":1,"source":"dbSNP","start":140454287,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794406677"},{"feature_type":"variation","strand":1,"end":140454288,"alleles":["C","A"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454288,"clinical_significance":[],"seq_region_name":"7","id":"rs1794406731"},{"seq_region_name":"7","id":"rs1794406793","clinical_significance":[],"alleles":["AAAAAA","AAAAAAAA"],"end":140454294,"strand":1,"feature_type":"variation","start":140454289,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"feature_type":"variation","strand":1,"end":140454290,"alleles":["A","G"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454290,"clinical_significance":[],"id":"rs999264434","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1211216405","seq_region_name":"7","end":140454300,"alleles":["AACTAACT","AACT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140454293,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1314336238","end":140454302,"alleles":["TTT","TTTT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140454300,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"end":140454302,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140454302,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs1794406949","clinical_significance":[]},{"clinical_significance":[],"id":"rs777609153","seq_region_name":"7","source":"dbSNP","start":140454303,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["AA","AAA"],"end":140454304,"feature_type":"variation","strand":1},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454308,"feature_type":"variation","strand":1,"end":140454308,"alleles":["T","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794407067"},{"feature_type":"variation","strand":1,"end":140454316,"alleles":["G","C","T"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454316,"clinical_significance":[],"seq_region_name":"7","id":"rs1234203602"},{"end":140454327,"alleles":["C","CC"],"strand":1,"feature_type":"variation","start":140454327,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs1369601768","clinical_significance":[]},{"start":140454328,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140454328,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794407240","clinical_significance":[]},{"seq_region_name":"7","id":"rs1563084684","clinical_significance":[],"alleles":["C","T"],"end":140454330,"strand":1,"feature_type":"variation","start":140454330,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"end":140454332,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140454332,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1028822226"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1383533875","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140454334,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454334},{"strand":1,"feature_type":"variation","end":140454336,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140454336,"source":"dbSNP","seq_region_name":"7","id":"rs1794407417","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140454337,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AACAACA","AACA"],"end":140454343,"seq_region_name":"7","id":"rs1794407464","clinical_significance":[]},{"id":"rs759734863","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140454344,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140454344},{"start":140454348,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["C","T"],"end":140454348,"strand":1,"feature_type":"variation","id":"rs76185706","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794407659","end":140454355,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140454355,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs767638242","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140454359,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454359},{"start":140454362,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["GAGGG","GAGGGAGGG"],"end":140454366,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794407743","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794407793","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140454364,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140454364},{"start":140454364,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["GGGG","GGG"],"end":140454367,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs756948499","clinical_significance":[]},{"alleles":["G","C"],"end":140454365,"feature_type":"variation","strand":1,"source":"dbSNP","start":140454365,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1377059959"},{"end":140454369,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140454369,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1171680639"},{"source":"dbSNP","start":140454371,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140454371,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1794407996","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["A","-"],"end":140454371,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454371,"clinical_significance":[],"seq_region_name":"7","id":"rs1794408039"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1453784421","source":"dbSNP","start":140454373,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140454373,"alleles":["A","G"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140454381,"alleles":["C","T"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454381,"clinical_significance":[],"seq_region_name":"7","id":"rs1794408174"},{"start":140454383,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140454383,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794408261","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140454385,"alleles":["G","A"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454385,"clinical_significance":[],"seq_region_name":"7","id":"rs1428427629"},{"alleles":["T","C"],"end":140454398,"strand":1,"feature_type":"variation","start":140454398,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs1794408412","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140454400,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140454400,"seq_region_name":"7","id":"rs1390843255","clinical_significance":[]},{"end":140454401,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140454401,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","id":"rs1168496520","seq_region_name":"7","clinical_significance":[]},{"id":"rs1376460336","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140454403,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140454403,"source":"dbSNP"},{"seq_region_name":"7","id":"rs532914726","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140454414,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140454414},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794408838","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454415,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140454415},{"start":140454419,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["G","A","C"],"end":140454419,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1398086139","clinical_significance":[]},{"seq_region_name":"7","id":"rs1486817896","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140454421,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140454421,"source":"dbSNP"},{"id":"rs1794409121","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140454422,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140454422,"source":"dbSNP"},{"start":140454433,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["A","G"],"end":140454433,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs372950794","clinical_significance":[]},{"seq_region_name":"7","id":"rs1331829173","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140454434,"source":"dbSNP","strand":1,"feature_type":"variation","end":140454434,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794409356","end":140454435,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140454435,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"alleles":["G","A"],"end":140454436,"strand":1,"feature_type":"variation","start":140454436,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs544987703","clinical_significance":[]},{"alleles":["A","C"],"end":140454442,"strand":1,"feature_type":"variation","start":140454442,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs1794409458","clinical_significance":[]},{"alleles":["G","A"],"end":140454443,"feature_type":"variation","strand":1,"source":"dbSNP","start":140454443,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1430988540"},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140454445,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454445,"clinical_significance":[],"seq_region_name":"7","id":"rs1343555454"},{"end":140454446,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140454446,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs375609871"},{"source":"dbSNP","start":140454448,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140454448,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794409643"},{"seq_region_name":"7","id":"rs1274688834","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140454450,"source":"dbSNP","strand":1,"feature_type":"variation","end":140454450,"alleles":["C","T"]},{"alleles":["C","A"],"end":140454451,"strand":1,"feature_type":"variation","start":140454451,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs1271473472","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794409795","feature_type":"variation","strand":1,"end":140454453,"alleles":["C","T"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454453},{"seq_region_name":"7","id":"rs925169856","clinical_significance":[],"start":140454453,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["CACCACCAC","CACCAC"],"end":140454461,"strand":1,"feature_type":"variation"},{"alleles":["CAC","CACAC"],"end":140454458,"strand":1,"feature_type":"variation","start":140454456,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","id":"rs935360280","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs34116813","seq_region_name":"7","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454458,"feature_type":"variation","strand":1,"end":140454459,"alleles":["CC","CCC"]},{"source":"dbSNP","start":140454464,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140454464,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794409996"},{"id":"rs752836500","seq_region_name":"7","clinical_significance":[],"end":140454466,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140454466,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"seq_region_name":"7","id":"rs757253227","clinical_significance":[],"start":140454470,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["G","A"],"end":140454470,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140454471,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140454471,"source":"dbSNP","seq_region_name":"7","id":"rs1362930237","clinical_significance":[]},{"seq_region_name":"7","id":"rs373438992","clinical_significance":[],"start":140454472,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140454472,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1164722857","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140454473,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140454473,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140454474,"alleles":["C","-"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140454474,"source":"dbSNP","seq_region_name":"7","id":"rs1433994511","clinical_significance":[]},{"end":140454477,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140454477,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs750268168"},{"seq_region_name":"7","id":"rs755751111","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140454479,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140454479,"source":"dbSNP"},{"clinical_significance":[],"id":"rs779594534","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140454482,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454482},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140454483,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140454483,"source":"dbSNP","seq_region_name":"7","id":"rs181454094","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794410589","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140454484,"source":"dbSNP","strand":1,"feature_type":"variation","end":140454499,"alleles":["TCAGCAGACCAGTTCA","TCA"]},{"feature_type":"variation","strand":1,"end":140454487,"alleles":["G","A","T"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454487,"clinical_significance":[],"seq_region_name":"7","id":"rs372477403"},{"start":140454493,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["C","T"],"end":140454493,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1328425516","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140454494,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140454494,"source":"dbSNP","seq_region_name":"7","id":"rs1189470425","clinical_significance":[]},{"end":140454495,"alleles":["G","GCAAGG"],"strand":1,"feature_type":"variation","start":140454495,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs917907337","clinical_significance":[]},{"source":"dbSNP","start":140454498,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140454498,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1585459109","seq_region_name":"7"},{"seq_region_name":"7","id":"rs778629902","clinical_significance":[],"start":140454500,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["C","T"],"end":140454500,"strand":1,"feature_type":"variation"},{"id":"rs201197588","seq_region_name":"7","clinical_significance":[],"alleles":["C","A","T"],"end":140454502,"strand":1,"feature_type":"variation","start":140454502,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"feature_type":"variation","strand":1,"end":140454502,"alleles":["C","CC"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454502,"clinical_significance":[],"seq_region_name":"7","id":"rs1794411017"},{"start":140454503,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["G","A"],"end":140454503,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs375734568","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140454504,"alleles":["C","T"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454504,"clinical_significance":[],"seq_region_name":"7","id":"rs773684309"},{"seq_region_name":"7","id":"rs1187723702","clinical_significance":[],"start":140454505,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140454505,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140454507,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140454507,"source":"dbSNP","seq_region_name":"7","id":"rs548821157","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs199805025","source":"dbSNP","start":140454508,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140454508,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1340856394","clinical_significance":[],"start":140454512,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140454512,"alleles":["G","C","T"],"strand":1,"feature_type":"variation"},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454513,"feature_type":"variation","strand":1,"end":140454513,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs776734885"},{"clinical_significance":[],"id":"rs1563084846","seq_region_name":"7","alleles":["T","C"],"end":140454514,"feature_type":"variation","strand":1,"source":"dbSNP","start":140454514,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140454520,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140454520,"seq_region_name":"7","id":"rs1794411524","clinical_significance":[]},{"seq_region_name":"7","id":"rs1194599812","clinical_significance":[],"end":140454521,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140454521,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"strand":1,"feature_type":"variation","end":140454524,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140454524,"source":"dbSNP","seq_region_name":"7","id":"rs759595831","clinical_significance":[]},{"alleles":["C","T"],"end":140454526,"feature_type":"variation","strand":1,"source":"dbSNP","start":140454526,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs373618317"},{"end":140454527,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140454527,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs931431975","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs752833626","end":140454528,"alleles":["A","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140454528,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140454531,"alleles":["C","A"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454531,"clinical_significance":[],"seq_region_name":"7","id":"rs1048657906"},{"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140454532,"source":"dbSNP","strand":1,"feature_type":"variation","end":140454532,"alleles":["A","G"],"id":"rs1443827522","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454533,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140454533,"clinical_significance":[],"seq_region_name":"7","id":"rs1165184863"},{"alleles":["C","A","T"],"end":140454540,"strand":1,"feature_type":"variation","start":140454540,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs377509145","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs767473878","feature_type":"variation","strand":1,"end":140454541,"alleles":["T","C"],"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454541},{"clinical_significance":[],"seq_region_name":"7","id":"rs200164454","end":140454542,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140454542,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"end":140454544,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140454544,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","id":"rs1794412785","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140454546,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","end":140454546,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs765294619"},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454552,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140454552,"clinical_significance":[],"id":"rs1167346575","seq_region_name":"7"},{"alleles":["T","C"],"end":140454554,"feature_type":"variation","strand":1,"source":"dbSNP","start":140454554,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs755872480"},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454555,"feature_type":"variation","strand":1,"end":140454555,"alleles":["G","A"],"clinical_significance":[],"id":"rs1794413140","seq_region_name":"7"},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454559,"feature_type":"variation","strand":1,"end":140454559,"alleles":["C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794413242"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794413334","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140454561,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454561},{"clinical_significance":[],"seq_region_name":"7","id":"rs796824934","source":"dbSNP","start":140454566,"consequence_type":"stop_gained","assembly_name":"GRCh38","end":140454566,"alleles":["C","T"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140454567,"source":"dbSNP","strand":1,"feature_type":"variation","end":140454567,"alleles":["A","G"],"seq_region_name":"7","id":"rs1416340162","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794413678","clinical_significance":["uncertain significance"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140454568,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140454568},{"seq_region_name":"7","id":"rs1794413768","clinical_significance":[],"start":140454570,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140454570,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1794413861","seq_region_name":"7","end":140454571,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140454571,"consequence_type":"synonymous_variant","assembly_name":"GRCh38"},{"id":"rs1336549971","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140454573,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140454573},{"start":140454574,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","end":140454574,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs2130235970","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs750130398","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"frameshift_variant","start":140454577,"source":"dbSNP","strand":1,"feature_type":"variation","end":140454580,"alleles":["AGAG","AG"]},{"id":"rs1382482745","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140454580,"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140454580,"source":"dbSNP"},{"end":140454584,"alleles":["G","A","C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140454584,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":["uncertain significance"],"seq_region_name":"7","id":"rs1794414242"},{"clinical_significance":["uncertain significance"],"seq_region_name":"7","id":"rs779688673","source":"dbSNP","start":140454585,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["T","A","C"],"end":140454585,"feature_type":"variation","strand":1},{"start":140454586,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","alleles":["T","C"],"end":140454586,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs141516487","clinical_significance":[]},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454591,"feature_type":"variation","strand":1,"end":140454591,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1350903351"},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140454592,"source":"dbSNP","strand":1,"feature_type":"variation","end":140454592,"alleles":["G","A","C"],"id":"rs546503746","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs901514411","clinical_significance":[],"strand":1,"feature_type":"variation","end":140454594,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140454594,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140454595,"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140454595,"source":"dbSNP","seq_region_name":"7","id":"rs374563168","clinical_significance":[]},{"start":140454596,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["T","C"],"end":140454596,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs747696884","clinical_significance":[]},{"seq_region_name":"7","id":"rs1463179144","clinical_significance":[],"start":140454601,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","alleles":["A","G"],"end":140454601,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140454602,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140454602,"source":"dbSNP","seq_region_name":"7","id":"rs1415902255","clinical_significance":[]},{"clinical_significance":[],"id":"rs772671179","seq_region_name":"7","end":140454606,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140454606,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs778450018","clinical_significance":[],"end":140454607,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140454607,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant"},{"end":140454609,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140454609,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794415153"},{"feature_type":"variation","strand":1,"end":140454613,"alleles":["A","C"],"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454613,"clinical_significance":[],"id":"rs1794415208","seq_region_name":"7"},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454617,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140454617,"clinical_significance":[],"seq_region_name":"7","id":"rs1585459463"},{"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454619,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140454619,"clinical_significance":[],"seq_region_name":"7","id":"rs1794415313"},{"end":140454622,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140454622,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","id":"rs747342744","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1164506273","seq_region_name":"7","source":"dbSNP","start":140454624,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140454624,"feature_type":"variation","strand":1},{"clinical_significance":["uncertain significance"],"seq_region_name":"7","id":"rs1382118469","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140454625,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454625},{"alleles":["T","C"],"end":140454627,"feature_type":"variation","strand":1,"source":"dbSNP","start":140454627,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs771206605"},{"clinical_significance":[],"id":"rs777122502","seq_region_name":"7","source":"dbSNP","start":140454631,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140454631,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs145362229","clinical_significance":["uncertain significance"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140454632,"source":"dbSNP","strand":1,"feature_type":"variation","end":140454632,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1426615557","consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454634,"feature_type":"variation","strand":1,"alleles":["C","A","G"],"end":140454634},{"seq_region_name":"7","id":"rs1192418715","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140454635,"source":"dbSNP","strand":1,"feature_type":"variation","end":140454635,"alleles":["A","C"]},{"id":"rs1249176961","seq_region_name":"7","clinical_significance":[],"end":140454636,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140454636,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs770050945","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454637,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140454637},{"clinical_significance":[],"seq_region_name":"7","id":"rs1467700407","end":140454640,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140454640,"consequence_type":"synonymous_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140454642,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["A","C","G"],"end":140454642,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794416075"},{"alleles":["G","A"],"end":140454643,"strand":1,"feature_type":"variation","start":140454643,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","seq_region_name":"7","id":"rs1794416153","clinical_significance":[]},{"start":140454644,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["G","A"],"end":140454644,"strand":1,"feature_type":"variation","id":"rs1174543136","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454646,"feature_type":"variation","strand":1,"end":140454646,"alleles":["G","A"],"clinical_significance":[],"id":"rs775516872","seq_region_name":"7"},{"source":"dbSNP","start":140454649,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140454649,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1457977974"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140454650,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140454650,"source":"dbSNP","seq_region_name":"7","id":"rs1062786","clinical_significance":[]},{"clinical_significance":[],"id":"rs1794416435","seq_region_name":"7","consequence_type":"inframe_deletion","assembly_name":"GRCh38","source":"dbSNP","start":140454653,"feature_type":"variation","strand":1,"alleles":["TCTTCTTC","TCTTC"],"end":140454660},{"feature_type":"variation","strand":1,"end":140454655,"alleles":["T","C","G"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454655,"clinical_significance":[],"id":"rs763042898","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1213731211","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140454658,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454658},{"end":140454661,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140454661,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1469439551","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1383304195","alleles":["T","A"],"end":140454662,"feature_type":"variation","strand":1,"source":"dbSNP","start":140454662,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140454663,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140454663,"source":"dbSNP","id":"rs773137189","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs147839699","source":"dbSNP","start":140454664,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","end":140454664,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1331163084","seq_region_name":"7","feature_type":"variation","strand":1,"end":140454666,"alleles":["T","G"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454666},{"end":140454673,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140454673,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794416918"},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140454674,"source":"dbSNP","strand":1,"feature_type":"variation","end":140454674,"alleles":["G","A","C"],"seq_region_name":"7","id":"rs766071821","clinical_significance":[]},{"alleles":["T","C"],"end":140454677,"feature_type":"variation","strand":1,"source":"dbSNP","start":140454677,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs753712171","seq_region_name":"7"},{"clinical_significance":["uncertain significance"],"seq_region_name":"7","id":"rs754552699","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454680,"feature_type":"variation","strand":1,"end":140454680,"alleles":["C","T"]},{"clinical_significance":["uncertain significance"],"seq_region_name":"7","id":"rs140396499","feature_type":"variation","strand":1,"end":140454681,"alleles":["T","C"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454681},{"source":"dbSNP","start":140454684,"consequence_type":"frameshift_variant","assembly_name":"GRCh38","alleles":["TCTCTCT","TCTCT","TCTCTCTCT"],"end":140454690,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs867495835"},{"clinical_significance":[],"id":"rs150349834","seq_region_name":"7","feature_type":"variation","strand":1,"end":140454685,"alleles":["C","T"],"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454685},{"clinical_significance":[],"seq_region_name":"7","id":"rs1062785","feature_type":"variation","strand":1,"end":140454686,"alleles":["T","G"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454686},{"end":140454688,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140454688,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs1794417422","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1335137496","source":"dbSNP","start":140454689,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140454689,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585459678","end":140454690,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140454690,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1324158358","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140454692,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454692},{"end":140454696,"alleles":["TCCTC","TC"],"strand":1,"feature_type":"variation","start":140454692,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"inframe_deletion","seq_region_name":"7","id":"rs755559870","clinical_significance":[]},{"seq_region_name":"7","id":"rs757997672","clinical_significance":[],"alleles":["C","G"],"end":140454694,"strand":1,"feature_type":"variation","start":140454694,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs538796576","feature_type":"variation","strand":1,"end":140454698,"alleles":["A","G"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454698},{"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140454701,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454701,"clinical_significance":[],"seq_region_name":"7","id":"rs1794417851"},{"feature_type":"variation","strand":1,"end":140454702,"alleles":["G","A"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454702,"clinical_significance":[],"seq_region_name":"7","id":"rs1062783"},{"id":"rs1481381013","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["GTTCCCAGAAGTGGTTCC","GTTCC"],"end":140454719,"assembly_name":"GRCh38","consequence_type":"frameshift_variant","start":140454702,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1794418017","seq_region_name":"7","feature_type":"variation","strand":1,"end":140454704,"alleles":["T","G"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454704},{"id":"rs1392389334","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140454707,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140454707,"source":"dbSNP"},{"seq_region_name":"7","id":"rs2130237038","clinical_significance":[],"end":140454708,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140454708,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"alleles":["G","A"],"end":140454709,"strand":1,"feature_type":"variation","start":140454709,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","seq_region_name":"7","id":"rs1219079015","clinical_significance":[]},{"alleles":["G","A"],"end":140454712,"feature_type":"variation","strand":1,"source":"dbSNP","start":140454712,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1428711371"},{"id":"rs866005951","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140454713,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140454713},{"clinical_significance":[],"seq_region_name":"7","id":"rs201485736","alleles":["G","T"],"end":140454714,"feature_type":"variation","strand":1,"source":"dbSNP","start":140454714,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs757843027","clinical_significance":[],"start":140454720,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140454720,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140454722,"alleles":["C","T"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454722,"clinical_significance":[],"seq_region_name":"7","id":"rs1062782"},{"end":140454724,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140454724,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","seq_region_name":"7","id":"rs1453574759","clinical_significance":[]},{"seq_region_name":"7","id":"rs781388618","clinical_significance":[],"start":140454729,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["C","A"],"end":140454729,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1794418633","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140454731,"consequence_type":"splice_acceptor_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454731},{"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140454733,"consequence_type":"splice_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454733,"clinical_significance":[],"seq_region_name":"7","id":"rs1794418671"},{"id":"rs779674250","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140454739,"alleles":["AAAAAA","AAAAAAA"],"assembly_name":"GRCh38","consequence_type":"splice_polypyrimidine_tract_variant","start":140454734,"source":"dbSNP"},{"start":140454742,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_polypyrimidine_tract_variant","end":140454742,"alleles":["A","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1300688698","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454742,"feature_type":"variation","strand":1,"alleles":["AGGCCATGATAGGGATGGCACT","AGGCCATGATAGGGATGGCACTAGGCCATGATAGGGATGGCACT"],"end":140454763,"clinical_significance":[],"seq_region_name":"7","id":"rs754337364"},{"seq_region_name":"7","id":"rs1794418918","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"splice_polypyrimidine_tract_variant","start":140454743,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140454743},{"clinical_significance":[],"seq_region_name":"7","id":"rs746285294","consequence_type":"splice_polypyrimidine_tract_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454744,"feature_type":"variation","strand":1,"end":140454744,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1469976669","feature_type":"variation","strand":1,"end":140454746,"alleles":["C","T"],"consequence_type":"splice_polypyrimidine_tract_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454746},{"end":140454747,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140454747,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1344356126"},{"end":140454750,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140454750,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1378670967"},{"end":140454754,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140454754,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs769954229","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1455146176","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140454757,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140454757},{"start":140454758,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140454758,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs569226868","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1314906679","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454759,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140454759},{"clinical_significance":[],"id":"rs749297645","seq_region_name":"7","end":140454760,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140454760,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs750365577","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454762,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140454762},{"source":"dbSNP","start":140454765,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140454765,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1490806437"},{"seq_region_name":"7","id":"rs373993370","clinical_significance":[],"alleles":["C","G","T"],"end":140454766,"strand":1,"feature_type":"variation","start":140454766,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454767,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140454767,"clinical_significance":[],"id":"rs760505774","seq_region_name":"7"},{"alleles":["C","T"],"end":140454770,"strand":1,"feature_type":"variation","start":140454770,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1286047504","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140454776,"alleles":["CAGTATC","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454770,"clinical_significance":[],"id":"rs1483452626","seq_region_name":"7"},{"seq_region_name":"7","id":"rs766375528","clinical_significance":[],"strand":1,"feature_type":"variation","end":140454772,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140454772,"source":"dbSNP"},{"clinical_significance":[],"id":"rs776245932","seq_region_name":"7","source":"dbSNP","start":140454773,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140454773,"alleles":["T","C"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140454774,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140454774,"source":"dbSNP","seq_region_name":"7","id":"rs1563085164","clinical_significance":[]},{"clinical_significance":[],"id":"rs759430006","seq_region_name":"7","source":"dbSNP","start":140454775,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140454775,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1165855891","feature_type":"variation","strand":1,"end":140454776,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454776},{"strand":1,"feature_type":"variation","end":140454780,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140454780,"source":"dbSNP","seq_region_name":"7","id":"rs1370583059","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794420570","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140454781,"source":"dbSNP","strand":1,"feature_type":"variation","end":140454781,"alleles":["A","G"]},{"start":140454785,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140454785,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794420619","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794420676","clinical_significance":[],"start":140454787,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140454787,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs73735253","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140454788,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454788},{"clinical_significance":[],"id":"rs758186697","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454790,"feature_type":"variation","strand":1,"end":140454790,"alleles":["T","C"]},{"alleles":["A","G"],"end":140454793,"strand":1,"feature_type":"variation","start":140454793,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs988075561","seq_region_name":"7","clinical_significance":[]},{"id":"rs1236411097","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140454794,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140454794,"source":"dbSNP"},{"seq_region_name":"7","id":"rs917959737","clinical_significance":[],"alleles":["G","C"],"end":140454797,"strand":1,"feature_type":"variation","start":140454797,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140454804,"alleles":["C","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140454804,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs970685518"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140454804,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140454804,"source":"dbSNP","id":"rs1435468147","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140454805,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454805,"clinical_significance":[],"seq_region_name":"7","id":"rs980852144"},{"alleles":["C","A","G"],"end":140454807,"strand":1,"feature_type":"variation","start":140454807,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1563085189","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1316527711","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140454809,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454809},{"source":"dbSNP","start":140454815,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140454815,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794422019"},{"start":140454817,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140454817,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs771405213","clinical_significance":[]},{"clinical_significance":[],"id":"rs1377482842","seq_region_name":"7","alleles":["G","A"],"end":140454820,"feature_type":"variation","strand":1,"source":"dbSNP","start":140454820,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1403366033","source":"dbSNP","start":140454823,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140454823,"feature_type":"variation","strand":1},{"id":"rs1470681676","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140454824,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140454824},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140454828,"source":"dbSNP","strand":1,"feature_type":"variation","end":140454828,"alleles":["C","T"],"seq_region_name":"7","id":"rs537047895","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140454829,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140454829,"source":"dbSNP","seq_region_name":"7","id":"rs1385935035","clinical_significance":[]},{"alleles":["C","G"],"end":140454832,"feature_type":"variation","strand":1,"source":"dbSNP","start":140454832,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794422663"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1192505217","source":"dbSNP","start":140454838,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140454838,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140454841,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140454848,"alleles":["TTAGTTAG","TTAG"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794422820"},{"id":"rs555267368","seq_region_name":"7","clinical_significance":[],"end":140454848,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140454848,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140454848,"source":"dbSNP","strand":1,"feature_type":"variation","end":140454850,"alleles":["GGG","GGGG"],"id":"rs1475472061","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794423127","clinical_significance":[],"alleles":["G","T"],"end":140454850,"strand":1,"feature_type":"variation","start":140454850,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1456268308","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140454851,"source":"dbSNP","strand":1,"feature_type":"variation","end":140454851,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1794423317","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140454863,"source":"dbSNP","strand":1,"feature_type":"variation","end":140454863,"alleles":["A","AA"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1190592656","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454867,"feature_type":"variation","strand":1,"end":140454867,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1794423478","clinical_significance":[],"strand":1,"feature_type":"variation","end":140454870,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140454870,"source":"dbSNP"},{"end":140454873,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140454873,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130238009","clinical_significance":[]},{"start":140454878,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140454878,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794423563","clinical_significance":[]},{"end":140454882,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140454882,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794423640","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140454883,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454883,"clinical_significance":[],"seq_region_name":"7","id":"rs1446144333"},{"clinical_significance":[],"seq_region_name":"7","id":"rs931510327","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454886,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140454886},{"seq_region_name":"7","id":"rs1794423908","clinical_significance":[],"end":140454887,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140454887,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1326053020","end":140454891,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140454891,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1049067015","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140454894,"source":"dbSNP","strand":1,"feature_type":"variation","end":140454894,"alleles":["C","A","T"]},{"seq_region_name":"7","id":"rs751216345","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140454895,"source":"dbSNP","strand":1,"feature_type":"variation","end":140454895,"alleles":["G","A","T"]},{"seq_region_name":"7","id":"rs1392218342","clinical_significance":[],"alleles":["T","C"],"end":140454897,"strand":1,"feature_type":"variation","start":140454897,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1364190525","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454901,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140454901},{"source":"dbSNP","start":140454903,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140454903,"alleles":["T","TT"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794424403"},{"end":140454910,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140454910,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs573615105"},{"seq_region_name":"7","id":"rs1794424511","clinical_significance":[],"end":140454914,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140454914,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1300487600","clinical_significance":[],"alleles":["C","T"],"end":140454916,"strand":1,"feature_type":"variation","start":140454916,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454918,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140454918,"clinical_significance":[],"seq_region_name":"7","id":"rs754634045"},{"end":140454918,"alleles":["C","-"],"strand":1,"feature_type":"variation","start":140454918,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1356495061","clinical_significance":[]},{"seq_region_name":"7","id":"rs1315240395","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","AA"],"end":140454919,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140454919,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140454920,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TTTTTT","TTTTT","TTTTTTT"],"end":140454925,"seq_region_name":"7","id":"rs1563085238","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140454922,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140454922,"seq_region_name":"7","id":"rs1229959255","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1290468491","source":"dbSNP","start":140454935,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140454935,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794424959","end":140454936,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140454936,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794425014","feature_type":"variation","strand":1,"end":140454939,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454939},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140454941,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454941,"clinical_significance":[],"id":"rs1794425058","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140454946,"source":"dbSNP","strand":1,"feature_type":"variation","end":140454946,"alleles":["A","AA"],"seq_region_name":"7","id":"rs1794425111","clinical_significance":[]},{"clinical_significance":[],"id":"rs1169804660","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454960,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140454960},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130238345","source":"dbSNP","start":140454963,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TTCCTCCTTTAATA","TTCCTCCTTTAATATTCCTCCTTTAATA"],"end":140454976,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140454964,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140454964,"source":"dbSNP","seq_region_name":"7","id":"rs908690139","clinical_significance":[]},{"seq_region_name":"7","id":"rs540800441","clinical_significance":[],"start":140454968,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140454968,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140454974,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140454974,"seq_region_name":"7","id":"rs1794425379","clinical_significance":[]},{"source":"dbSNP","start":140454975,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140454975,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1421029609"},{"clinical_significance":[],"id":"rs1794425534","seq_region_name":"7","source":"dbSNP","start":140454977,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140454977,"alleles":["C","G"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454978,"feature_type":"variation","strand":1,"end":140454978,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1165786128"},{"clinical_significance":[],"seq_region_name":"7","id":"rs940305020","source":"dbSNP","start":140454980,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A","C"],"end":140454980,"feature_type":"variation","strand":1},{"end":140454981,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140454981,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794425812","clinical_significance":[]},{"id":"rs1041273600","seq_region_name":"7","clinical_significance":[],"start":140454985,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140454985,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140454987,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454987,"clinical_significance":[],"seq_region_name":"7","id":"rs558932955"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454988,"feature_type":"variation","strand":1,"end":140454988,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs780626165"},{"source":"dbSNP","start":140454989,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140454989,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794426032"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140454991,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454991,"clinical_significance":[],"seq_region_name":"7","id":"rs997115529"},{"end":140454992,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140454992,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs186283328"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140454996,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140454996,"source":"dbSNP","seq_region_name":"7","id":"rs1794426188","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","A","G","T"],"end":140454998,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140454998,"clinical_significance":[],"id":"rs544739706","seq_region_name":"7"},{"seq_region_name":"7","id":"rs563049644","clinical_significance":[],"alleles":["T","G"],"end":140455000,"strand":1,"feature_type":"variation","start":140455000,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["G","A"],"end":140455001,"strand":1,"feature_type":"variation","start":140455001,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs574856214","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1794426426","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140455004,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455004},{"strand":1,"feature_type":"variation","end":140455005,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140455005,"source":"dbSNP","seq_region_name":"7","id":"rs1585460223","clinical_significance":[]},{"seq_region_name":"7","id":"rs542246739","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140455009,"source":"dbSNP","strand":1,"feature_type":"variation","end":140455009,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130238595","source":"dbSNP","start":140455011,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140455015,"alleles":["CTTCT","CT"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1214187380","feature_type":"variation","strand":1,"end":140455023,"alleles":["CCCC","CCC"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455020},{"clinical_significance":[],"seq_region_name":"7","id":"rs1455555412","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455021,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140455021},{"clinical_significance":[],"id":"rs1335774109","seq_region_name":"7","alleles":["C","T"],"end":140455023,"feature_type":"variation","strand":1,"source":"dbSNP","start":140455023,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130238661","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140455029,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455029},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794426694","source":"dbSNP","start":140455031,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140455031,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1295378942","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140455035,"source":"dbSNP","strand":1,"feature_type":"variation","end":140455035,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1413267316","end":140455036,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140455036,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794426841","end":140455038,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140455038,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["G","A"],"end":140455041,"feature_type":"variation","strand":1,"source":"dbSNP","start":140455041,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1032630738"},{"strand":1,"feature_type":"variation","end":140455043,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140455043,"source":"dbSNP","id":"rs1794427061","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs956561009","alleles":["A","G"],"end":140455046,"feature_type":"variation","strand":1,"source":"dbSNP","start":140455046,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140455048,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140455048,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs377415065","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs755409759","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455053,"feature_type":"variation","strand":1,"alleles":["A","AA"],"end":140455053},{"source":"dbSNP","start":140455056,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140455056,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs752405122"},{"seq_region_name":"7","id":"rs758193966","clinical_significance":[],"end":140455058,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140455058,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140455059,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140455059,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1563085295"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140455060,"source":"dbSNP","strand":1,"feature_type":"variation","end":140455061,"alleles":["AA","A"],"id":"rs779405544","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794427695","alleles":["A","G"],"end":140455061,"feature_type":"variation","strand":1,"source":"dbSNP","start":140455061,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs763685470","alleles":["T","C"],"end":140455062,"feature_type":"variation","strand":1,"source":"dbSNP","start":140455062,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140455063,"source":"dbSNP","strand":1,"feature_type":"variation","end":140455063,"alleles":["T","C"],"id":"rs1031865447","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs751132552","source":"dbSNP","start":140455067,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140455067,"alleles":["C","T"],"feature_type":"variation","strand":1},{"start":140455069,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140455069,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs757674986","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs372013752","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455071,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140455071},{"clinical_significance":[],"seq_region_name":"7","id":"rs748462683","end":140455081,"alleles":["AAAAAAA","AAAAAAAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140455075,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs746160296","source":"dbSNP","start":140455077,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140455077,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1418065879","clinical_significance":[],"end":140455078,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140455078,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140455080,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140455080,"seq_region_name":"7","id":"rs756474870","clinical_significance":[]},{"start":140455081,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140455081,"alleles":["A","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794428375","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455081,"feature_type":"variation","strand":1,"end":140455083,"alleles":["ACA","A"],"clinical_significance":[],"id":"rs536708159","seq_region_name":"7"},{"source":"dbSNP","start":140455082,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140455082,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1794428575","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs777822430","source":"dbSNP","start":140455083,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AG","-"],"end":140455084,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140455084,"source":"dbSNP","strand":1,"feature_type":"variation","end":140455084,"alleles":["G","C"],"seq_region_name":"7","id":"rs1794428701","clinical_significance":[]},{"id":"rs747301958","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"splice_donor_5th_base_variant","start":140455086,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GAGAG","GAG"],"end":140455090},{"seq_region_name":"7","id":"rs552028038","clinical_significance":[],"start":140455095,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_region_variant","alleles":["C","T"],"end":140455095,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs201520447","clinical_significance":[],"end":140455096,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140455096,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"strand":1,"feature_type":"variation","end":140455097,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140455097,"source":"dbSNP","seq_region_name":"7","id":"rs1206627084","clinical_significance":["uncertain significance"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1231259326","end":140455099,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140455099,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs190612309","clinical_significance":[],"alleles":["A","G"],"end":140455100,"strand":1,"feature_type":"variation","start":140455100,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"clinical_significance":[],"id":"rs1468980046","seq_region_name":"7","alleles":["C","T"],"end":140455102,"feature_type":"variation","strand":1,"source":"dbSNP","start":140455102,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1794429445","seq_region_name":"7","source":"dbSNP","start":140455107,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","end":140455107,"alleles":["T","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs778824995","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140455110,"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140455110,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1245319120","clinical_significance":[],"start":140455114,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["C","T"],"end":140455114,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140455118,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140455118,"source":"dbSNP","seq_region_name":"7","id":"rs748286595","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140455121,"alleles":["T","G"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455121,"clinical_significance":[],"seq_region_name":"7","id":"rs1062780"},{"start":140455123,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["T","C"],"end":140455123,"strand":1,"feature_type":"variation","id":"rs1183504347","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs528414465","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455125,"feature_type":"variation","strand":1,"end":140455125,"alleles":["T","A"]},{"seq_region_name":"7","id":"rs1585460476","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140455128,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140455128},{"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455131,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140455131,"clinical_significance":[],"id":"rs1275215862","seq_region_name":"7"},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455132,"feature_type":"variation","strand":1,"end":140455132,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1391255762"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140455133,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455133,"clinical_significance":[],"id":"rs770728123","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1231689118","feature_type":"variation","strand":1,"end":140455136,"alleles":["C","G","T"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455136},{"clinical_significance":[],"seq_region_name":"7","id":"rs1171846914","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455138,"feature_type":"variation","strand":1,"end":140455138,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1062779","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140455143,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455143},{"clinical_significance":[],"seq_region_name":"7","id":"rs375633730","alleles":["C","T"],"end":140455144,"feature_type":"variation","strand":1,"source":"dbSNP","start":140455144,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140455145,"alleles":["G","A"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455145,"clinical_significance":["uncertain significance"],"seq_region_name":"7","id":"rs769711070"},{"start":140455146,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","alleles":["G","A"],"end":140455146,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs775485297","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140455149,"alleles":["A","G"],"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455149,"clinical_significance":[],"seq_region_name":"7","id":"rs762674256"},{"seq_region_name":"7","id":"rs1794430890","clinical_significance":[],"start":140455151,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["C","T"],"end":140455151,"strand":1,"feature_type":"variation"},{"alleles":["G","C"],"end":140455154,"strand":1,"feature_type":"variation","start":140455154,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","id":"rs776192325","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140455155,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140455155,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1314110435"},{"source":"dbSNP","start":140455156,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140455156,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585460561"},{"start":140455158,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","alleles":["C","T"],"end":140455158,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs376108886","clinical_significance":[]},{"end":140455159,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140455159,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs750995669"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140455160,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455160,"clinical_significance":[],"id":"rs1062778","seq_region_name":"7"},{"id":"rs1270916343","seq_region_name":"7","clinical_significance":[],"end":140455162,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140455162,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455164,"feature_type":"variation","strand":1,"end":140455164,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs761398321"},{"clinical_significance":[],"id":"rs1794431680","seq_region_name":"7","end":140455165,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140455165,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"alleles":["G","A"],"end":140455167,"feature_type":"variation","strand":1,"source":"dbSNP","start":140455167,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs534521262"},{"seq_region_name":"7","id":"rs370316104","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140455177,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140455177},{"clinical_significance":[],"seq_region_name":"7","id":"rs149055577","feature_type":"variation","strand":1,"end":140455179,"alleles":["C","T"],"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455179},{"alleles":["C","T"],"end":140455180,"feature_type":"variation","strand":1,"source":"dbSNP","start":140455180,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1062777","seq_region_name":"7"},{"seq_region_name":"7","id":"rs780370803","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140455183,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140455183,"source":"dbSNP"},{"end":140455189,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140455189,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794432246"},{"source":"dbSNP","start":140455191,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","end":140455191,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs754237108"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1476653127","consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455197,"feature_type":"variation","strand":1,"end":140455197,"alleles":["C","A","G"]},{"clinical_significance":["uncertain significance"],"id":"rs1285876700","seq_region_name":"7","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455201,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140455201},{"clinical_significance":[],"id":"rs1794432653","seq_region_name":"7","alleles":["G","A"],"end":140455202,"feature_type":"variation","strand":1,"source":"dbSNP","start":140455202,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1185328876","clinical_significance":[],"start":140455205,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140455205,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140455218,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140455218,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1416747785","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140455219,"source":"dbSNP","strand":1,"feature_type":"variation","end":140455219,"alleles":["C","A","T"],"seq_region_name":"7","id":"rs1062776","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794433061","clinical_significance":[],"alleles":["G","A"],"end":140455221,"strand":1,"feature_type":"variation","start":140455221,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1062775","feature_type":"variation","strand":1,"end":140455224,"alleles":["C","G","T"],"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455224},{"alleles":["G","A"],"end":140455225,"strand":1,"feature_type":"variation","start":140455225,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs373781587","clinical_significance":[]},{"clinical_significance":[],"id":"rs1407763162","seq_region_name":"7","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455231,"feature_type":"variation","strand":1,"end":140455231,"alleles":["T","C"]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140455234,"assembly_name":"GRCh38","consequence_type":"splice_acceptor_variant","start":140455234,"source":"dbSNP","id":"rs1794433482","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1467912248","feature_type":"variation","strand":1,"end":140455236,"alleles":["G","A"],"consequence_type":"splice_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455236},{"feature_type":"variation","strand":1,"end":140455242,"alleles":["G","C"],"consequence_type":"splice_polypyrimidine_tract_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455242,"clinical_significance":[],"id":"rs1794433606","seq_region_name":"7"},{"end":140455249,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140455249,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_polypyrimidine_tract_variant","seq_region_name":"7","id":"rs1335777122","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140455250,"consequence_type":"splice_polypyrimidine_tract_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455250,"clinical_significance":[],"seq_region_name":"7","id":"rs748121903"},{"id":"rs772200247","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140455251,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140455251,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1159608316","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140455255,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140455255,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1585460764","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455256,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140455256},{"id":"rs1268392062","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140455261,"strand":1,"feature_type":"variation","start":140455261,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["C","G"],"end":140455263,"strand":1,"feature_type":"variation","start":140455263,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794434171","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs369132756","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455268,"feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140455268},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455272,"feature_type":"variation","strand":1,"end":140455272,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1219956781"},{"source":"dbSNP","start":140455273,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140455273,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1285286993"},{"start":140455274,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140455274,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1312547579","clinical_significance":[]},{"seq_region_name":"7","id":"rs769902287","clinical_significance":[],"start":140455275,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140455275,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140455277,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455277,"clinical_significance":[],"seq_region_name":"7","id":"rs1794434673"},{"id":"rs2130239992","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["GGTCTGTATTTG","G"],"end":140455288,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140455277,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140455281,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455281,"clinical_significance":[],"seq_region_name":"7","id":"rs775395309"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455282,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140455282,"clinical_significance":[],"id":"rs373048859","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1449149777","clinical_significance":[],"end":140455283,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140455283,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140455287,"alleles":["TTT","TTTT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140455285,"source":"dbSNP","seq_region_name":"7","id":"rs1794435020","clinical_significance":[]},{"end":140455290,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140455290,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1305994638","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455296,"feature_type":"variation","strand":1,"end":140455296,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1041299801"},{"alleles":["C","T"],"end":140455298,"feature_type":"variation","strand":1,"source":"dbSNP","start":140455298,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs922827665"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1349645423","source":"dbSNP","start":140455299,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140455299,"alleles":["G","A"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["G","A","C","T"],"end":140455301,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455301,"clinical_significance":[],"seq_region_name":"7","id":"rs954884482"},{"id":"rs986184846","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140455310,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140455310},{"clinical_significance":[],"id":"rs1794435618","seq_region_name":"7","feature_type":"variation","strand":1,"end":140455311,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455311},{"end":140455313,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140455313,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1306830026"},{"seq_region_name":"7","id":"rs778314189","clinical_significance":[],"start":140455317,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140455317,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140455318,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140455318,"seq_region_name":"7","id":"rs1371071906","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130240209","source":"dbSNP","start":140455319,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140455319,"feature_type":"variation","strand":1},{"id":"rs138095467","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140455321,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140455321,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455322,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140455322,"clinical_significance":[],"seq_region_name":"7","id":"rs1438216449"},{"end":140455323,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140455323,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1366424825","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140455325,"source":"dbSNP","strand":1,"feature_type":"variation","end":140455325,"alleles":["G","C"],"seq_region_name":"7","id":"rs775089031","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455327,"feature_type":"variation","strand":1,"end":140455327,"alleles":["A","G"],"clinical_significance":[],"id":"rs1794437031","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1455102630","source":"dbSNP","start":140455328,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140455328,"feature_type":"variation","strand":1},{"end":140455331,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140455331,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs2130240311","seq_region_name":"7","clinical_significance":[]},{"end":140455333,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140455333,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1794437226","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs550769125","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455334,"feature_type":"variation","strand":1,"end":140455334,"alleles":["T","C","G"]},{"feature_type":"variation","strand":1,"end":140455337,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455337,"clinical_significance":[],"seq_region_name":"7","id":"rs2130240357"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455338,"feature_type":"variation","strand":1,"end":140455338,"alleles":["A","AA"],"clinical_significance":[],"id":"rs1794437435","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794437508","feature_type":"variation","strand":1,"end":140455340,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455340},{"clinical_significance":[],"seq_region_name":"7","id":"rs569389461","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455346,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140455346},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455347,"feature_type":"variation","strand":1,"end":140455347,"alleles":["C","A"],"clinical_significance":[],"id":"rs924799180","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1242651955","clinical_significance":[],"alleles":["C","T"],"end":140455349,"strand":1,"feature_type":"variation","start":140455349,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140455350,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140455350,"strand":1,"feature_type":"variation","id":"rs1001054657","seq_region_name":"7","clinical_significance":[]},{"id":"rs1794437803","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140455351,"source":"dbSNP","strand":1,"feature_type":"variation","end":140455354,"alleles":["CCCC","CCCCC","CCCCCC"]},{"end":140455354,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140455354,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs934791131","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs892294170","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455356,"feature_type":"variation","strand":1,"end":140455356,"alleles":["A","C"]},{"seq_region_name":"7","id":"rs1432695496","clinical_significance":[],"start":140455360,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140455360,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"id":"rs1262622198","seq_region_name":"7","clinical_significance":[],"end":140455362,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140455362,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["T","C"],"end":140455366,"feature_type":"variation","strand":1,"source":"dbSNP","start":140455366,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs536633225"},{"end":140455367,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140455367,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794438137"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794438194","end":140455370,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140455370,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1794438237","seq_region_name":"7","clinical_significance":[],"start":140455374,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140455374,"strand":1,"feature_type":"variation"},{"id":"rs1024912002","seq_region_name":"7","clinical_significance":[],"start":140455374,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AT","-"],"end":140455375,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1260563301","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140455375,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140455375},{"feature_type":"variation","strand":1,"end":140455377,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455377,"clinical_significance":[],"seq_region_name":"7","id":"rs1794438400"},{"alleles":["G","A"],"end":140455378,"strand":1,"feature_type":"variation","start":140455378,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs970664036","clinical_significance":[]},{"clinical_significance":[],"id":"rs2130240591","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455380,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140455380},{"start":140455386,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140455386,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794438505","clinical_significance":[]},{"start":140455387,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140455387,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1350728390","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455390,"feature_type":"variation","strand":1,"end":140455395,"alleles":["AAGAAA","AA"],"clinical_significance":[],"seq_region_name":"7","id":"rs1278846790"},{"alleles":["G","A"],"end":140455392,"strand":1,"feature_type":"variation","start":140455392,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1002104686","clinical_significance":[]},{"id":"rs1794438712","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140455398,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140455398,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs61378275","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455399,"feature_type":"variation","strand":1,"end":140455399,"alleles":["T","TT"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130240654","source":"dbSNP","start":140455399,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140455399,"alleles":["T","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1794438838","seq_region_name":"7","source":"dbSNP","start":140455401,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140455401,"feature_type":"variation","strand":1},{"end":140455406,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140455406,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1295765984","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1188234570","clinical_significance":[],"end":140455407,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140455407,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs567800428","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455409,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140455409},{"start":140455410,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140455410,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1257784553","clinical_significance":[]},{"end":140455411,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140455411,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs993493905","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs142685493","feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140455412,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455412},{"start":140455416,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["CTCT","CT"],"end":140455419,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs984619863","clinical_significance":[]},{"id":"rs948984008","seq_region_name":"7","clinical_significance":[],"alleles":["T","A","C"],"end":140455417,"strand":1,"feature_type":"variation","start":140455417,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455419,"feature_type":"variation","strand":1,"end":140455419,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794439600"},{"strand":1,"feature_type":"variation","end":140455424,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140455424,"source":"dbSNP","id":"rs1794439670","seq_region_name":"7","clinical_significance":[]},{"start":140455424,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AA","AAA"],"end":140455425,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794439745","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140455425,"source":"dbSNP","strand":1,"feature_type":"variation","end":140455425,"alleles":["A","G"],"seq_region_name":"7","id":"rs1015639568","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1373118522","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140455426,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455426},{"start":140455430,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140455430,"alleles":["A","G"],"strand":1,"feature_type":"variation","id":"rs1794439994","seq_region_name":"7","clinical_significance":[]},{"id":"rs1044093068","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140455431,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140455431,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140455439,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140455439,"source":"dbSNP","seq_region_name":"7","id":"rs1431620416","clinical_significance":[]},{"start":140455448,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140455448,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs961856482","clinical_significance":[]},{"end":140455449,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140455449,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794440337"},{"start":140455450,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140455450,"alleles":["T","C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794440414","clinical_significance":[]},{"alleles":["A","G"],"end":140455454,"feature_type":"variation","strand":1,"source":"dbSNP","start":140455454,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs888100552"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1427008392","source":"dbSNP","start":140455454,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AGCAG","AG"],"end":140455458,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1166621774","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140455458,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140455458},{"seq_region_name":"7","id":"rs762622240","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140455465,"source":"dbSNP","strand":1,"feature_type":"variation","end":140455465,"alleles":["T","C","G"]},{"seq_region_name":"7","id":"rs976916930","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["AGAGAGA","AGAGA"],"end":140455472,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140455466,"source":"dbSNP"},{"id":"rs146046912","seq_region_name":"7","clinical_significance":[],"start":140455467,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140455467,"alleles":["G","A","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130241030","feature_type":"variation","strand":1,"end":140455468,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455468},{"alleles":["G","A","C"],"end":140455469,"strand":1,"feature_type":"variation","start":140455469,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs922754002","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs941103233","end":140455471,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140455471,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1305448283","seq_region_name":"7","source":"dbSNP","start":140455472,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140455472,"alleles":["A","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1251445786","end":140455475,"alleles":["AAAA","AAAAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140455472,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1415094606","clinical_significance":[],"end":140455473,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140455473,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140455481,"alleles":["TCTTCT","TCT"],"strand":1,"feature_type":"variation","start":140455476,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs985667867","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794441438","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140455483,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140455483},{"strand":1,"feature_type":"variation","end":140455495,"alleles":["A","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140455495,"source":"dbSNP","id":"rs763815319","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs910215695","clinical_significance":[],"start":140455495,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140455496,"alleles":["AT","-"],"strand":1,"feature_type":"variation"},{"id":"rs2272096","seq_region_name":"7","clinical_significance":[],"start":140455496,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140455496,"alleles":["T","A","C"],"strand":1,"feature_type":"variation"},{"id":"rs559215181","seq_region_name":"7","clinical_significance":[],"end":140455502,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140455502,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs182270900","feature_type":"variation","strand":1,"end":140455504,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455504},{"seq_region_name":"7","id":"rs1794442155","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140455506,"source":"dbSNP","strand":1,"feature_type":"variation","end":140455506,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs538457957","clinical_significance":[],"end":140455507,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140455507,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140455509,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140455509,"alleles":["C","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1300006430","clinical_significance":[]},{"start":140455511,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C"],"end":140455511,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs889731310","clinical_significance":[]},{"clinical_significance":[],"id":"rs1794442596","seq_region_name":"7","source":"dbSNP","start":140455519,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140455519,"alleles":["A","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1423117483","source":"dbSNP","start":140455520,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140455520,"alleles":["C","T"],"feature_type":"variation","strand":1},{"alleles":["G","A"],"end":140455521,"feature_type":"variation","strand":1,"source":"dbSNP","start":140455521,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794442702"},{"clinical_significance":[],"id":"rs1794442779","seq_region_name":"7","source":"dbSNP","start":140455526,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140455526,"feature_type":"variation","strand":1},{"id":"rs1165947650","seq_region_name":"7","clinical_significance":[],"start":140455528,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140455528,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140455530,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455530,"clinical_significance":[],"seq_region_name":"7","id":"rs1794442963"},{"start":140455532,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140455532,"alleles":["A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794443038","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794443117","end":140455533,"alleles":["-","CC"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140455534,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["T","C"],"end":140455536,"strand":1,"feature_type":"variation","start":140455536,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs556619104","clinical_significance":[]},{"end":140455538,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140455538,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794443261","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140455541,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140455541,"source":"dbSNP","id":"rs1416235778","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140455542,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140455542,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1381557597"},{"end":140455545,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140455545,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs138819896","seq_region_name":"7"},{"alleles":["T","C"],"end":140455547,"strand":1,"feature_type":"variation","start":140455547,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs945096698","clinical_significance":[]},{"seq_region_name":"7","id":"rs1046288287","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140455551,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140455551,"source":"dbSNP"},{"start":140455553,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140455553,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1366019457","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455556,"feature_type":"variation","strand":1,"end":140455556,"alleles":["C","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794443844"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1231332275","feature_type":"variation","strand":1,"end":140455562,"alleles":["CTTACTT","CTT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455556},{"seq_region_name":"7","id":"rs1563085599","clinical_significance":[],"end":140455558,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140455558,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455560,"feature_type":"variation","strand":1,"end":140455560,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794444086"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140455561,"source":"dbSNP","strand":1,"feature_type":"variation","end":140455561,"alleles":["T","C"],"seq_region_name":"7","id":"rs1256954008","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["TT","TTT"],"end":140455562,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455561,"clinical_significance":[],"id":"rs906362920","seq_region_name":"7"},{"seq_region_name":"7","id":"rs2130241551","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140455566,"source":"dbSNP","strand":1,"feature_type":"variation","end":140455566,"alleles":["A","T"]},{"id":"rs1017569657","seq_region_name":"7","clinical_significance":[],"end":140455568,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140455568,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794444415","source":"dbSNP","start":140455570,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140455570,"alleles":["G","A"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140455571,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140455571,"source":"dbSNP","seq_region_name":"7","id":"rs968665276","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130241598","feature_type":"variation","strand":1,"end":140455572,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455572},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140455576,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140455576,"seq_region_name":"7","id":"rs1214006217","clinical_significance":[]},{"start":140455577,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140455577,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1341904441","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794444711","feature_type":"variation","strand":1,"end":140455578,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455578},{"alleles":["TTT","T"],"end":140455583,"strand":1,"feature_type":"variation","start":140455581,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1336657098","clinical_significance":[]},{"start":140455583,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140455583,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs772444845","clinical_significance":[]},{"end":140455585,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140455585,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs978817673","clinical_significance":[]},{"start":140455586,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140455586,"strand":1,"feature_type":"variation","id":"rs1794445018","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140455591,"alleles":["ACACA","ACA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455587,"clinical_significance":[],"id":"rs2130241672","seq_region_name":"7"},{"end":140455588,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140455588,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1033567787"},{"clinical_significance":[],"id":"rs1794445194","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455593,"feature_type":"variation","strand":1,"end":140455593,"alleles":["T","C"]},{"source":"dbSNP","start":140455594,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140455594,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1794445271","seq_region_name":"7"},{"start":140455598,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140455598,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1336235417","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455600,"feature_type":"variation","strand":1,"end":140455600,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1309083364"},{"seq_region_name":"7","id":"rs1794445422","clinical_significance":[],"strand":1,"feature_type":"variation","end":140455601,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140455601,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140455601,"alleles":["C","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455601,"clinical_significance":[],"seq_region_name":"7","id":"rs1794445494"},{"id":"rs1794445570","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140455603,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140455603,"source":"dbSNP"},{"source":"dbSNP","start":140455604,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140455604,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794445653"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140455605,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140455605,"id":"rs1031683209","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140455606,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140455606,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1463267645"},{"seq_region_name":"7","id":"rs1482093269","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140455607,"source":"dbSNP","strand":1,"feature_type":"variation","end":140455610,"alleles":["CCCC","CCCCC"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794446049","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455608,"feature_type":"variation","strand":1,"end":140455608,"alleles":["C","A"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140455609,"source":"dbSNP","strand":1,"feature_type":"variation","end":140455609,"alleles":["C","T"],"seq_region_name":"7","id":"rs542210367","clinical_significance":[]},{"seq_region_name":"7","id":"rs775338027","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140455613,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140455613},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563085647","feature_type":"variation","strand":1,"end":140455614,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455614},{"alleles":["A","G"],"end":140455615,"feature_type":"variation","strand":1,"source":"dbSNP","start":140455615,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130241883"},{"source":"dbSNP","start":140455617,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140455617,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794446370"},{"alleles":["G","C"],"end":140455618,"strand":1,"feature_type":"variation","start":140455618,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1163083009","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794446509","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140455620,"source":"dbSNP","strand":1,"feature_type":"variation","end":140455620,"alleles":["G","A"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140455621,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140455621,"seq_region_name":"7","id":"rs956309980","clinical_significance":[]},{"alleles":["T","A"],"end":140455622,"strand":1,"feature_type":"variation","start":140455622,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794446655","clinical_significance":[]},{"end":140455624,"alleles":["T","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140455624,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs142033240"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794446841","feature_type":"variation","strand":1,"end":140455626,"alleles":["G","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455626},{"feature_type":"variation","strand":1,"end":140455627,"alleles":["C","CC"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455627,"clinical_significance":[],"id":"rs1794446934","seq_region_name":"7"},{"alleles":["T","C"],"end":140455634,"strand":1,"feature_type":"variation","start":140455634,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs917388069","clinical_significance":[]},{"seq_region_name":"7","id":"rs949028170","clinical_significance":[],"start":140455635,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140455635,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455636,"feature_type":"variation","strand":1,"end":140455636,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1261886526"},{"feature_type":"variation","strand":1,"end":140455643,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455643,"clinical_significance":[],"seq_region_name":"7","id":"rs1794447236"},{"clinical_significance":[],"id":"rs961507731","seq_region_name":"7","source":"dbSNP","start":140455644,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140455644,"alleles":["G","A","C"],"feature_type":"variation","strand":1},{"id":"rs1794447439","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140455645,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140455645},{"seq_region_name":"7","id":"rs1450726528","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","AA"],"end":140455650,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140455650,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1794447499","clinical_significance":[],"strand":1,"feature_type":"variation","end":140455650,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140455650,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1794447600","clinical_significance":[],"strand":1,"feature_type":"variation","end":140455653,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140455653,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563085661","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455655,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140455655},{"clinical_significance":[],"seq_region_name":"7","id":"rs976801262","alleles":["A","G"],"end":140455658,"feature_type":"variation","strand":1,"source":"dbSNP","start":140455658,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs2130242128","clinical_significance":[],"start":140455658,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140455661,"alleles":["AAAA","AAAAA"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1213905309","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140455664,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140455664},{"start":140455666,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140455666,"strand":1,"feature_type":"variation","id":"rs1794447776","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1794447832","seq_region_name":"7","source":"dbSNP","start":140455668,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140455668,"alleles":["G","A"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455669,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140455669,"clinical_significance":[],"id":"rs1794447884","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs980733195","feature_type":"variation","strand":1,"end":140455672,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455672},{"seq_region_name":"7","id":"rs1469565759","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140455674,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140455674},{"clinical_significance":[],"seq_region_name":"7","id":"rs1287336663","source":"dbSNP","start":140455676,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140455676,"alleles":["A","G","T"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455679,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140455679,"clinical_significance":[],"seq_region_name":"7","id":"rs1794448071"},{"start":140455680,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140455680,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794448118","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455682,"feature_type":"variation","strand":1,"end":140455682,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs78914315"},{"end":140455686,"alleles":["AA","AAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140455685,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794448211"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455687,"feature_type":"variation","strand":1,"alleles":["G","C","T"],"end":140455687,"clinical_significance":[],"seq_region_name":"7","id":"rs1395735286"},{"source":"dbSNP","start":140455688,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140455688,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs572804355"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455690,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140455690,"clinical_significance":[],"id":"rs1794448387","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140455700,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455700,"clinical_significance":[],"seq_region_name":"7","id":"rs1794448442"},{"clinical_significance":[],"id":"rs1351145209","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455704,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140455704},{"clinical_significance":[],"seq_region_name":"7","id":"rs1262353904","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140455706,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455706},{"clinical_significance":[],"seq_region_name":"7","id":"rs1237959707","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455708,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140455708},{"seq_region_name":"7","id":"rs1794448640","clinical_significance":[],"start":140455715,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140455715,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455721,"feature_type":"variation","strand":1,"end":140455721,"alleles":["C","T"],"clinical_significance":[],"id":"rs1029817908","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1186595892","source":"dbSNP","start":140455724,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A","C"],"end":140455724,"feature_type":"variation","strand":1},{"id":"rs909567687","seq_region_name":"7","clinical_significance":[],"start":140455734,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140455734,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140455737,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455737,"clinical_significance":[],"seq_region_name":"7","id":"rs1794448856"},{"end":140455746,"alleles":["C","A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140455746,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794448908"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794448956","feature_type":"variation","strand":1,"end":140455747,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455747},{"clinical_significance":[],"seq_region_name":"7","id":"rs1214260896","source":"dbSNP","start":140455750,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140455750,"alleles":["G","C"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140455751,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140455751,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1242116222"},{"strand":1,"feature_type":"variation","end":140455754,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140455754,"source":"dbSNP","id":"rs775669508","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs150864182","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140455758,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140455758,"source":"dbSNP"},{"alleles":["C","T"],"end":140455761,"strand":1,"feature_type":"variation","start":140455761,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs371628915","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794449279","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455761,"feature_type":"variation","strand":1,"end":140455761,"alleles":["C","-"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140455762,"source":"dbSNP","strand":1,"feature_type":"variation","end":140455762,"alleles":["G","A","T"],"seq_region_name":"7","id":"rs761437544","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1479227698","source":"dbSNP","start":140455765,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140455765,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140455766,"alleles":["G","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455766,"clinical_significance":[],"seq_region_name":"7","id":"rs749983524"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140455767,"source":"dbSNP","strand":1,"feature_type":"variation","end":140455767,"alleles":["A","T"],"id":"rs761136056","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs766899412","source":"dbSNP","start":140455768,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140455768,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455769,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140455769,"clinical_significance":[],"seq_region_name":"7","id":"rs1050970502"},{"strand":1,"feature_type":"variation","end":140455771,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140455771,"source":"dbSNP","seq_region_name":"7","id":"rs754151015","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130242573","clinical_significance":[],"start":140455775,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140455775,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140455777,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140455777,"id":"rs755386761","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs778939101","clinical_significance":[],"start":140455780,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140455780,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1304991375","alleles":["T","C"],"end":140455787,"feature_type":"variation","strand":1,"source":"dbSNP","start":140455787,"consequence_type":"splice_donor_region_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1343765893","source":"dbSNP","start":140455797,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140455797,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140455799,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455799,"clinical_significance":[],"seq_region_name":"7","id":"rs1223112666"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794450059","consequence_type":"inframe_deletion","assembly_name":"GRCh38","source":"dbSNP","start":140455801,"feature_type":"variation","strand":1,"alleles":["CTT","-"],"end":140455803},{"seq_region_name":"7","id":"rs535393077","clinical_significance":[],"end":140455803,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140455803,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"alleles":["G","A"],"end":140455804,"strand":1,"feature_type":"variation","start":140455804,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","seq_region_name":"7","id":"rs565206300","clinical_significance":[]},{"alleles":["C","A"],"end":140455810,"strand":1,"feature_type":"variation","start":140455810,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","seq_region_name":"7","id":"rs1353287022","clinical_significance":[]},{"clinical_significance":["likely benign"],"seq_region_name":"7","id":"rs1062774","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455811,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140455811},{"source":"dbSNP","start":140455812,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","end":140455812,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs758609358"},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455815,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140455815,"clinical_significance":[],"seq_region_name":"7","id":"rs1794450412"},{"alleles":["T","C"],"end":140455823,"feature_type":"variation","strand":1,"source":"dbSNP","start":140455823,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs777887661"},{"consequence_type":"frameshift_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455825,"feature_type":"variation","strand":1,"alleles":["CTTCTCTTCT","CTTCT"],"end":140455834,"clinical_significance":[],"seq_region_name":"7","id":"rs770899620"},{"seq_region_name":"7","id":"rs1794450584","clinical_significance":[],"strand":1,"feature_type":"variation","end":140455840,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140455840,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1225401969","alleles":["C","T"],"end":140455842,"feature_type":"variation","strand":1,"source":"dbSNP","start":140455842,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140455843,"source":"dbSNP","strand":1,"feature_type":"variation","end":140455843,"alleles":["C","T"],"seq_region_name":"7","id":"rs1794450721","clinical_significance":[]},{"seq_region_name":"7","id":"rs1379117720","clinical_significance":[],"start":140455844,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140455844,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140455845,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140455845,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1794450912","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1238330035","clinical_significance":[],"start":140455848,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140455848,"alleles":["A","C","T"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140455849,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140455849,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1270372220"},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140455852,"source":"dbSNP","strand":1,"feature_type":"variation","end":140455852,"alleles":["C","G"],"seq_region_name":"7","id":"rs889586956","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1489664552","source":"dbSNP","start":140455855,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140455855,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1198220173","clinical_significance":[],"alleles":["A","G"],"end":140455867,"strand":1,"feature_type":"variation","start":140455867,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794451538","source":"dbSNP","start":140455872,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140455872,"feature_type":"variation","strand":1},{"id":"rs747126783","seq_region_name":"7","clinical_significance":[],"start":140455873,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","end":140455873,"alleles":["A","C","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1455208261","clinical_significance":[],"end":140455881,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140455881,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"feature_type":"variation","strand":1,"end":140455882,"alleles":["C","G","T"],"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455882,"clinical_significance":[],"id":"rs1062773","seq_region_name":"7"},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455884,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140455884,"clinical_significance":[],"seq_region_name":"7","id":"rs756080779"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1156543096","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140455888,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455888},{"clinical_significance":[],"seq_region_name":"7","id":"rs1062772","feature_type":"variation","strand":1,"end":140455890,"alleles":["C","G"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455890},{"clinical_significance":[],"seq_region_name":"7","id":"rs780164618","end":140455895,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140455895,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"alleles":["G","A"],"end":140455898,"feature_type":"variation","strand":1,"source":"dbSNP","start":140455898,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1244558610"},{"end":140455905,"alleles":["GGG","GG"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140455903,"consequence_type":"splice_region_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs776709388"},{"alleles":["G","A"],"end":140455904,"feature_type":"variation","strand":1,"source":"dbSNP","start":140455904,"consequence_type":"splice_region_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs374275333"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1447364840","source":"dbSNP","start":140455912,"consequence_type":"splice_polypyrimidine_tract_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140455912,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140455913,"alleles":["G","C","T"],"consequence_type":"splice_polypyrimidine_tract_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455913,"clinical_significance":[],"seq_region_name":"7","id":"rs768491565"},{"seq_region_name":"7","id":"rs1794452848","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"splice_polypyrimidine_tract_variant","start":140455915,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140455915},{"seq_region_name":"7","id":"rs532174102","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140455918,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140455918,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140455919,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455919,"clinical_significance":[],"seq_region_name":"7","id":"rs1352949678"},{"feature_type":"variation","strand":1,"end":140455923,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455923,"clinical_significance":[],"seq_region_name":"7","id":"rs747813728"},{"clinical_significance":[],"seq_region_name":"7","id":"rs771659901","alleles":["T","C"],"end":140455926,"feature_type":"variation","strand":1,"source":"dbSNP","start":140455926,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs772664450","clinical_significance":[],"alleles":["T","C"],"end":140455933,"strand":1,"feature_type":"variation","start":140455933,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs760197940","clinical_significance":[],"start":140455934,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140455934,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs766811600","clinical_significance":[],"end":140455943,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140455943,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1794453581","seq_region_name":"7","source":"dbSNP","start":140455946,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140455946,"feature_type":"variation","strand":1},{"id":"rs777129608","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140455949,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140455949,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1274480805","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455951,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140455951},{"seq_region_name":"7","id":"rs1043583109","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140455953,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140455953,"source":"dbSNP"},{"source":"dbSNP","start":140455954,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140455954,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1356635873"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140455957,"source":"dbSNP","strand":1,"feature_type":"variation","end":140455957,"alleles":["A","G"],"seq_region_name":"7","id":"rs760029943","clinical_significance":[]},{"seq_region_name":"7","id":"rs765625644","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140455960,"source":"dbSNP","strand":1,"feature_type":"variation","end":140455960,"alleles":["G","A","T"]},{"alleles":["A","G"],"end":140455961,"feature_type":"variation","strand":1,"source":"dbSNP","start":140455961,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794454210"},{"clinical_significance":[],"id":"rs1585461806","seq_region_name":"7","alleles":["A","C"],"end":140455965,"feature_type":"variation","strand":1,"source":"dbSNP","start":140455965,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1794454382","seq_region_name":"7","source":"dbSNP","start":140455966,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140455966,"alleles":["C","A"],"feature_type":"variation","strand":1},{"id":"rs1794454470","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140455974,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140455974},{"end":140455975,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140455975,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794454551","clinical_significance":[]},{"id":"rs1794454644","seq_region_name":"7","clinical_significance":[],"end":140455982,"alleles":["TCGCCTC","TC"],"strand":1,"feature_type":"variation","start":140455976,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1316731071","alleles":["C","T"],"end":140455977,"feature_type":"variation","strand":1,"source":"dbSNP","start":140455977,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794454790","source":"dbSNP","start":140455977,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["CGCC","-"],"end":140455980,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140455978,"alleles":["G","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455978,"clinical_significance":[],"seq_region_name":"7","id":"rs2363826"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140455982,"feature_type":"variation","strand":1,"end":140455982,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794455104"},{"end":140455983,"alleles":["CC","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140455982,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794455168"},{"start":140455983,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140455983,"alleles":["C","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794455257","clinical_significance":[]},{"seq_region_name":"7","id":"rs1176089297","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140455985,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140455985},{"source":"dbSNP","start":140455988,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TT","T"],"end":140455989,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794455450"},{"clinical_significance":[],"id":"rs1794455536","seq_region_name":"7","alleles":["T","C"],"end":140455989,"feature_type":"variation","strand":1,"source":"dbSNP","start":140455989,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140455990,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AAA","AA","AAAA"],"end":140455992,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs879071436"},{"id":"rs117771053","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140455991,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140455991,"source":"dbSNP"},{"end":140455999,"alleles":["AAGACTTAA","AAGACTTAAGACTTAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140455991,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794455811"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140455996,"source":"dbSNP","strand":1,"feature_type":"variation","end":140455996,"alleles":["T","G"],"seq_region_name":"7","id":"rs1794455903","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs17621014","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456000,"feature_type":"variation","strand":1,"end":140456000,"alleles":["C","A","T"]},{"start":140456001,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140456001,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794456139","clinical_significance":[]},{"alleles":["A","C"],"end":140456003,"feature_type":"variation","strand":1,"source":"dbSNP","start":140456003,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1794456198","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1475567013","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140456004,"source":"dbSNP","strand":1,"feature_type":"variation","end":140456004,"alleles":["A","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1055470362","alleles":["A","G","T"],"end":140456005,"feature_type":"variation","strand":1,"source":"dbSNP","start":140456005,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563085892","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456008,"feature_type":"variation","strand":1,"end":140456008,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1794456415","clinical_significance":[],"start":140456009,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140456009,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs888398139","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456010,"feature_type":"variation","strand":1,"end":140456010,"alleles":["C","T"]},{"start":140456010,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140456010,"alleles":["C","-"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1303951896","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs564429344","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456011,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140456011},{"strand":1,"feature_type":"variation","end":140456012,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140456012,"source":"dbSNP","id":"rs1794456696","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130243693","alleles":["T","A"],"end":140456018,"feature_type":"variation","strand":1,"source":"dbSNP","start":140456018,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140456024,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140456024,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs139345958","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456028,"feature_type":"variation","strand":1,"end":140456028,"alleles":["G","A"],"clinical_significance":[],"id":"rs1465884163","seq_region_name":"7"},{"start":140456031,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140456031,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794456852","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140456034,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140456034,"seq_region_name":"7","id":"rs1563085915","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456036,"feature_type":"variation","strand":1,"end":140456036,"alleles":["C","T"],"clinical_significance":[],"id":"rs1014742270","seq_region_name":"7"},{"seq_region_name":"7","id":"rs573238460","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140456037,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140456037},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140456041,"source":"dbSNP","strand":1,"feature_type":"variation","end":140456041,"alleles":["T","C"],"id":"rs1212940290","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1206232961","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140456043,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456043},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140456049,"source":"dbSNP","strand":1,"feature_type":"variation","end":140456049,"alleles":["A","G"],"id":"rs2130243788","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","T"],"end":140456053,"feature_type":"variation","strand":1,"source":"dbSNP","start":140456053,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1440758655"},{"end":140456062,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140456062,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs970607521"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140456064,"source":"dbSNP","strand":1,"feature_type":"variation","end":140456064,"alleles":["T","C"],"id":"rs1585461971","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","C"],"end":140456066,"feature_type":"variation","strand":1,"source":"dbSNP","start":140456066,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1278064856"},{"source":"dbSNP","start":140456068,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140456068,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1215350790"},{"seq_region_name":"7","id":"rs1276564985","clinical_significance":[],"start":140456069,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140456069,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140456070,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140456070,"seq_region_name":"7","id":"rs1246861131","clinical_significance":[]},{"id":"rs1794457913","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140456072,"source":"dbSNP","strand":1,"feature_type":"variation","end":140456072,"alleles":["G","C"]},{"start":140456073,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140456073,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794457953","clinical_significance":[]},{"clinical_significance":[],"id":"rs150044172","seq_region_name":"7","source":"dbSNP","start":140456074,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140456074,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140456075,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140456075,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs770311444"},{"end":140456077,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140456077,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs751327687","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs897152968","source":"dbSNP","start":140456078,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140456078,"alleles":["C","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1332979126","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456086,"feature_type":"variation","strand":1,"end":140456086,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1410075196","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456089,"feature_type":"variation","strand":1,"end":140456089,"alleles":["A","C"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456090,"feature_type":"variation","strand":1,"end":140456090,"alleles":["T","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130244000"},{"source":"dbSNP","start":140456091,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140456091,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1421143619"},{"seq_region_name":"7","id":"rs962949348","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140456093,"source":"dbSNP","strand":1,"feature_type":"variation","end":140456093,"alleles":["A","C"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140456095,"source":"dbSNP","strand":1,"feature_type":"variation","end":140456095,"alleles":["C","A","T"],"id":"rs972434741","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["CTC","C"],"end":140456097,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140456095,"source":"dbSNP","seq_region_name":"7","id":"rs1794458537","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140456096,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456096,"clinical_significance":[],"seq_region_name":"7","id":"rs1585462076"},{"seq_region_name":"7","id":"rs2130244057","clinical_significance":[],"start":140456098,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140456098,"strand":1,"feature_type":"variation"},{"end":140456100,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140456100,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794458617"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794458676","source":"dbSNP","start":140456107,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140456107,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140456111,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TT","TTT"],"end":140456112,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794458733"},{"start":140456111,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TTCTT","TT"],"end":140456115,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1477335372","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["TCT","T"],"end":140456114,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456112,"clinical_significance":[],"seq_region_name":"7","id":"rs1418379665"},{"clinical_significance":[],"id":"rs970465216","seq_region_name":"7","source":"dbSNP","start":140456113,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140456113,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140456113,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","-"],"end":140456113,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1432326769","seq_region_name":"7"},{"source":"dbSNP","start":140456114,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140456128,"alleles":["TTTTTTTTTTTTTTT","TTTTTTTTTTT","TTTTTTTTTTTT","TTTTTTTTTTTTT","TTTTTTTTTTTTTT","TTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTT"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs57991505"},{"seq_region_name":"7","id":"rs80120731","clinical_significance":[],"start":140456115,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140456115,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1585462148","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140456116,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140456116,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1175632728","end":140456118,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140456118,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140456118,"alleles":["-","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140456119,"source":"dbSNP","id":"rs1794459453","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794459512","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140456119,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140456119},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456121,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140456121,"clinical_significance":[],"seq_region_name":"7","id":"rs1794459567"},{"start":140456122,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["-","G"],"end":140456121,"strand":1,"feature_type":"variation","id":"rs1389603564","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140456122,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456122,"clinical_significance":[],"seq_region_name":"7","id":"rs1227076202"},{"clinical_significance":[],"seq_region_name":"7","id":"rs980102250","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456129,"feature_type":"variation","strand":1,"end":140456129,"alleles":["G","T"]},{"feature_type":"variation","strand":1,"end":140456129,"alleles":["G","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456129,"clinical_significance":[],"id":"rs1794459809","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1458998432","clinical_significance":[],"end":140456130,"alleles":["GA","-"],"strand":1,"feature_type":"variation","start":140456129,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140456130,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140456130,"alleles":["A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794459907"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130244332","alleles":["A","G"],"end":140456136,"feature_type":"variation","strand":1,"source":"dbSNP","start":140456136,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140456137,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140456137,"source":"dbSNP","id":"rs1387989490","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456140,"feature_type":"variation","strand":1,"end":140456140,"alleles":["C","A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794460078"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794460151","source":"dbSNP","start":140456141,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140456142,"alleles":["TT","-"],"feature_type":"variation","strand":1},{"alleles":["AAAAAA","AAAAAAA"],"end":140456152,"feature_type":"variation","strand":1,"source":"dbSNP","start":140456147,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs556675115"},{"end":140456156,"alleles":["AAACAAA","AAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140456150,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794460343"},{"source":"dbSNP","start":140456152,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140456152,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1442228427"},{"clinical_significance":[],"seq_region_name":"7","id":"rs920689194","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456153,"feature_type":"variation","strand":1,"end":140456153,"alleles":["C","A"]},{"seq_region_name":"7","id":"rs1328868528","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140456156,"source":"dbSNP","strand":1,"feature_type":"variation","end":140456156,"alleles":["A","C"]},{"source":"dbSNP","start":140456159,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140456159,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585462223"},{"end":140456163,"alleles":["AAAA","-"],"strand":1,"feature_type":"variation","start":140456160,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1464822852","clinical_significance":[]},{"end":140456168,"alleles":["AAGAAGA","AAGA"],"strand":1,"feature_type":"variation","start":140456162,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1029660832","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794461223","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140456163,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456163},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140456163,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AGA","A"],"end":140456165,"seq_region_name":"7","id":"rs1794461292","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140456164,"alleles":["G","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456164,"clinical_significance":[],"seq_region_name":"7","id":"rs1166597474"},{"seq_region_name":"7","id":"rs534204731","clinical_significance":[],"start":140456169,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140456169,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140456174,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CACACA","CACA"],"end":140456179,"id":"rs1403415672","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs954228038","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456182,"feature_type":"variation","strand":1,"alleles":["CTCCT","CT"],"end":140456186},{"feature_type":"variation","strand":1,"end":140456184,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456184,"clinical_significance":[],"seq_region_name":"7","id":"rs2130244580"},{"source":"dbSNP","start":140456185,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140456185,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1412902655","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1177713317","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140456186,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140456186},{"id":"rs1794461879","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140456191,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140456191,"source":"dbSNP"},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456195,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140456195,"clinical_significance":[],"seq_region_name":"7","id":"rs552570079"},{"seq_region_name":"7","id":"rs571154767","clinical_significance":[],"strand":1,"feature_type":"variation","end":140456196,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140456196,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1794461990","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140456197,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140456197,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140456198,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140456198,"id":"rs1794462042","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1469109233","clinical_significance":[],"strand":1,"feature_type":"variation","end":140456199,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140456199,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1178237478","seq_region_name":"7","alleles":["TAAATAAAT","TAAAT"],"end":140456207,"feature_type":"variation","strand":1,"source":"dbSNP","start":140456199,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"start":140456200,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140456202,"alleles":["AAA","AAAA"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1275320657","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794462282","source":"dbSNP","start":140456201,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140456201,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1033584339","seq_region_name":"7","feature_type":"variation","strand":1,"end":140456209,"alleles":["TTT","TTTT"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456207},{"end":140456210,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140456210,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs957669830"},{"clinical_significance":[],"id":"rs1794462476","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140456213,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456213},{"seq_region_name":"7","id":"rs1794462531","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140456217,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140456217},{"id":"rs1365929546","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140456226,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CTCT","CT"],"end":140456229},{"id":"rs1794462659","seq_region_name":"7","clinical_significance":[],"start":140456229,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["T","C"],"end":140456229,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140456233,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140456233,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1794462715","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140456235,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456235,"clinical_significance":[],"id":"rs1794462784","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1051261212","seq_region_name":"7","alleles":["T","A"],"end":140456238,"feature_type":"variation","strand":1,"source":"dbSNP","start":140456238,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1794462929","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140456244,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140456244,"source":"dbSNP"},{"start":140456248,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140456248,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs911058515","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794463054","clinical_significance":[],"start":140456249,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["T","G"],"end":140456249,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794463098","end":140456250,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140456250,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs2130244925","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","-"],"end":140456250,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140456250,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794463159","end":140456260,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140456260,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1378444800","seq_region_name":"7","source":"dbSNP","start":140456267,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140456267,"alleles":["A","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1288617787","feature_type":"variation","strand":1,"end":140456268,"alleles":["T","A","C"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456268},{"clinical_significance":[],"seq_region_name":"7","id":"rs1330838222","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456269,"feature_type":"variation","strand":1,"end":140456269,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1226159781","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456272,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140456272},{"clinical_significance":[],"seq_region_name":"7","id":"rs942493248","source":"dbSNP","start":140456279,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140456279,"alleles":["T","A","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1456133156","alleles":["G","A","T"],"end":140456281,"feature_type":"variation","strand":1,"source":"dbSNP","start":140456281,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1451664758","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456283,"feature_type":"variation","strand":1,"end":140456283,"alleles":["G","T"]},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140456284,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140456284,"source":"dbSNP","seq_region_name":"7","id":"rs1223694738","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140456287,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140456287,"source":"dbSNP","seq_region_name":"7","id":"rs754578959","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1159723939","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456289,"feature_type":"variation","strand":1,"end":140456289,"alleles":["T","C"]},{"clinical_significance":[],"id":"rs1794463838","seq_region_name":"7","end":140456294,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140456294,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1421495433","source":"dbSNP","start":140456302,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140456302,"alleles":["T","A"],"feature_type":"variation","strand":1},{"end":140456312,"alleles":["ATA","A"],"strand":1,"feature_type":"variation","start":140456310,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs1378521063","clinical_significance":[]},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456311,"feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140456311,"clinical_significance":[],"seq_region_name":"7","id":"rs767190133"},{"strand":1,"feature_type":"variation","end":140456314,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140456314,"source":"dbSNP","seq_region_name":"7","id":"rs1794464080","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140456319,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140456319,"source":"dbSNP","seq_region_name":"7","id":"rs1454783607","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130245157","clinical_significance":[],"strand":1,"feature_type":"variation","end":140456320,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140456320,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1255057460","alleles":["GG","G"],"end":140456321,"feature_type":"variation","strand":1,"source":"dbSNP","start":140456320,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"alleles":["G","C"],"end":140456321,"strand":1,"feature_type":"variation","start":140456321,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs1043532532","clinical_significance":[]},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456330,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140456330,"clinical_significance":[],"seq_region_name":"7","id":"rs1794464479"},{"start":140456331,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["A","G"],"end":140456331,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794464566","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794464642","clinical_significance":[],"strand":1,"feature_type":"variation","end":140456346,"alleles":["ACGTCAGGAAACATAC","AC"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140456331,"source":"dbSNP"},{"start":140456332,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140456332,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1488357939","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140456333,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140456333,"source":"dbSNP","seq_region_name":"7","id":"rs903818769","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1218519786","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456342,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140456342},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794464939","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140456344,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456344},{"start":140456346,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140456351,"alleles":["CATTCA","CA"],"strand":1,"feature_type":"variation","id":"rs540488364","seq_region_name":"7","clinical_significance":[]},{"end":140456349,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140456349,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1794465081","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1794465135","clinical_significance":[],"end":140456353,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140456353,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140456355,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140456355,"source":"dbSNP","seq_region_name":"7","id":"rs569542124","clinical_significance":[]},{"start":140456356,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["T","A"],"end":140456356,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794465275","clinical_significance":[]},{"clinical_significance":[],"id":"rs937730040","seq_region_name":"7","end":140456358,"alleles":["G","C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140456358,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140456359,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140456359,"source":"dbSNP","id":"rs2130245383","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1488053637","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","A","G"],"end":140456361,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456361},{"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140456362,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456362,"clinical_significance":[],"seq_region_name":"7","id":"rs1302944282"},{"start":140456364,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["T","C"],"end":140456364,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794465549","clinical_significance":[]},{"start":140456367,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["G","C"],"end":140456367,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794465618","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794465678","alleles":["A","G"],"end":140456371,"feature_type":"variation","strand":1,"source":"dbSNP","start":140456371,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1794465733","seq_region_name":"7","feature_type":"variation","strand":1,"end":140456372,"alleles":["C","T"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456372},{"start":140456373,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140456373,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1384773957","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs796535878","source":"dbSNP","start":140456377,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140456377,"alleles":["C","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1366613094","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140456378,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140456378,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1794466000","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140456380,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140456380,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794466054","alleles":["A","G"],"end":140456381,"feature_type":"variation","strand":1,"source":"dbSNP","start":140456381,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794466121","feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140456384,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456384},{"strand":1,"feature_type":"variation","alleles":["G","C","T"],"end":140456386,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140456386,"source":"dbSNP","id":"rs999379418","seq_region_name":"7","clinical_significance":[]},{"start":140456388,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["TAATAAT","TAAT"],"end":140456394,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794466275","clinical_significance":[]},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456390,"feature_type":"variation","strand":1,"end":140456392,"alleles":["ATA","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1289274402"},{"id":"rs1794466400","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140456392,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140456392,"source":"dbSNP"},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456394,"feature_type":"variation","strand":1,"alleles":["T","-"],"end":140456394,"clinical_significance":[],"seq_region_name":"7","id":"rs1401651254"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794466456","source":"dbSNP","start":140456394,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140456394,"alleles":["T","C"],"feature_type":"variation","strand":1},{"end":140456396,"alleles":["CC","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140456395,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794466636"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140456398,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140456398,"source":"dbSNP","seq_region_name":"7","id":"rs1794466692","clinical_significance":[]},{"source":"dbSNP","start":140456399,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140456399,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1358497354"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794466767","feature_type":"variation","strand":1,"end":140456402,"alleles":["AAA","AAAA"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456400},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140456405,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140456405,"id":"rs1053079371","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140456406,"alleles":["A","G"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456406,"clinical_significance":[],"seq_region_name":"7","id":"rs1794466911"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1054989559","alleles":["AA","A"],"end":140456407,"feature_type":"variation","strand":1,"source":"dbSNP","start":140456406,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1585462596","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140456407,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140456407,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1794467132","clinical_significance":[],"end":140456412,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140456412,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"source":"dbSNP","start":140456417,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140456417,"alleles":["A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1413862200"},{"seq_region_name":"7","id":"rs1794467348","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140456417,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AAAAA","AAAAAA"],"end":140456421},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456422,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140456422,"clinical_significance":[],"seq_region_name":"7","id":"rs909703830"},{"start":140456425,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140456425,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","id":"rs1235307576","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs941320530","source":"dbSNP","start":140456426,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140456426,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140456427,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456427,"clinical_significance":[],"seq_region_name":"7","id":"rs1794467660"},{"seq_region_name":"7","id":"rs1037321343","clinical_significance":[],"start":140456429,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140456429,"alleles":["G","C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1263011831","end":140456433,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140456433,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"start":140456434,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140456434,"alleles":["T","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794467984","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140456437,"alleles":["C","G"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456437,"clinical_significance":[],"seq_region_name":"7","id":"rs2130245923"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794468074","source":"dbSNP","start":140456441,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140456441,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794468175","alleles":["A","AA"],"end":140456442,"feature_type":"variation","strand":1,"source":"dbSNP","start":140456442,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1794468273","clinical_significance":[],"start":140456443,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140456443,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs897162974","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456446,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140456446},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140456451,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140456451,"seq_region_name":"7","id":"rs1794468454","clinical_significance":[]},{"seq_region_name":"7","id":"rs1485704286","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140456452,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140456452},{"start":140456455,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140456455,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794468665","clinical_significance":[]},{"start":140456456,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140456456,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1257294581","clinical_significance":[]},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456462,"feature_type":"variation","strand":1,"end":140456462,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794468838"},{"end":140456463,"alleles":["A","C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140456463,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs998115883"},{"clinical_significance":[],"id":"rs2130246119","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140456466,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456466},{"seq_region_name":"7","id":"rs1794469100","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140456468,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140456468,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794469198","alleles":["G","C"],"end":140456472,"feature_type":"variation","strand":1,"source":"dbSNP","start":140456472,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"start":140456474,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["T","C"],"end":140456474,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs538030424","clinical_significance":[]},{"seq_region_name":"7","id":"rs889899051","clinical_significance":[],"start":140456476,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140456476,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456478,"feature_type":"variation","strand":1,"end":140456478,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs185986740"},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456479,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140456479,"clinical_significance":[],"seq_region_name":"7","id":"rs1338152856"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1297502739","feature_type":"variation","strand":1,"end":140456480,"alleles":["A","C"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456480},{"seq_region_name":"7","id":"rs1794469804","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140456491,"source":"dbSNP","strand":1,"feature_type":"variation","end":140456491,"alleles":["A","C"]},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140456492,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456492,"clinical_significance":[],"seq_region_name":"7","id":"rs1794469890"},{"id":"rs1014360021","seq_region_name":"7","clinical_significance":[],"start":140456494,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["C","G","T"],"end":140456494,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140456498,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140456498,"source":"dbSNP","seq_region_name":"7","id":"rs1794470110","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130246304","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456500,"feature_type":"variation","strand":1,"end":140456500,"alleles":["G","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1024772099","end":140456501,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140456501,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794470314","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456503,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140456503},{"seq_region_name":"7","id":"rs970261439","clinical_significance":[],"alleles":["T","C"],"end":140456517,"strand":1,"feature_type":"variation","start":140456517,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"feature_type":"variation","strand":1,"alleles":["CCCC","CCC"],"end":140456521,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456518,"clinical_significance":[],"seq_region_name":"7","id":"rs1794470532"},{"seq_region_name":"7","id":"rs1794470624","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140456520,"source":"dbSNP","strand":1,"feature_type":"variation","end":140456520,"alleles":["C","G"]},{"source":"dbSNP","start":140456521,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140456521,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794470721"},{"seq_region_name":"7","id":"rs1309066223","clinical_significance":[],"alleles":["A","T"],"end":140456522,"strand":1,"feature_type":"variation","start":140456522,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"strand":1,"feature_type":"variation","end":140456523,"alleles":["T","A","C"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140456523,"source":"dbSNP","seq_region_name":"7","id":"rs1465626150","clinical_significance":[]},{"seq_region_name":"7","id":"rs1001740089","clinical_significance":[],"strand":1,"feature_type":"variation","end":140456527,"alleles":["A","C","G"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140456527,"source":"dbSNP"},{"end":140456530,"alleles":["-","AC"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140456531,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794471045"},{"clinical_significance":[],"seq_region_name":"7","id":"rs770291144","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456534,"feature_type":"variation","strand":1,"alleles":["CA","-"],"end":140456535},{"end":140456540,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140456540,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs144344762","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140456541,"alleles":["A","C"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456541,"clinical_significance":[],"seq_region_name":"7","id":"rs1794471257"},{"clinical_significance":[],"id":"rs1794471332","seq_region_name":"7","feature_type":"variation","strand":1,"end":140456542,"alleles":["A","C","G"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456542},{"seq_region_name":"7","id":"rs535901709","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140456543,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140456543},{"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140456545,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456545,"clinical_significance":[],"seq_region_name":"7","id":"rs1794471470"},{"seq_region_name":"7","id":"rs1423421164","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140456554,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140456554},{"strand":1,"feature_type":"variation","end":140456555,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140456555,"source":"dbSNP","id":"rs2130246576","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140456557,"alleles":["A","AA"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456557,"clinical_significance":[],"seq_region_name":"7","id":"rs957765696"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794471590","source":"dbSNP","start":140456557,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140456557,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1287259773","source":"dbSNP","start":140456560,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140456560,"alleles":["T","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1010496862","clinical_significance":[],"strand":1,"feature_type":"variation","end":140456561,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140456561,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs775877449","feature_type":"variation","strand":1,"end":140456563,"alleles":["AAA","AAAA"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456561},{"strand":1,"feature_type":"variation","end":140456566,"alleles":["C","A","G","T"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140456566,"source":"dbSNP","seq_region_name":"7","id":"rs1020510880","clinical_significance":[]},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456567,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140456567,"clinical_significance":[],"seq_region_name":"7","id":"rs1200214855"},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456568,"feature_type":"variation","strand":1,"end":140456568,"alleles":["G","C"],"clinical_significance":[],"id":"rs1794472077","seq_region_name":"7"},{"source":"dbSNP","start":140456572,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140456572,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585462830"},{"end":140456579,"alleles":["T","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140456579,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs966385028"},{"clinical_significance":[],"id":"rs1277384495","seq_region_name":"7","source":"dbSNP","start":140456580,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140456580,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140456581,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140456581,"id":"rs1233706392","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794472401","source":"dbSNP","start":140456586,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140456586,"alleles":["T","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1342139295","end":140456590,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140456590,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs981745871","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140456591,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140456591},{"seq_region_name":"7","id":"rs1794472591","clinical_significance":[],"start":140456594,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140456594,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"end":140456595,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140456595,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585462865"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794472721","alleles":["T","G"],"end":140456599,"feature_type":"variation","strand":1,"source":"dbSNP","start":140456599,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140456604,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140456604,"seq_region_name":"7","id":"rs1439154234","clinical_significance":[]},{"id":"rs753055644","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140456605,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140456605},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140456606,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140456606,"seq_region_name":"7","id":"rs757063200","clinical_significance":[]},{"id":"rs758616705","seq_region_name":"7","clinical_significance":[],"alleles":["T","A"],"end":140456607,"strand":1,"feature_type":"variation","start":140456607,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"end":140456608,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140456608,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794473001"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563086200","source":"dbSNP","start":140456608,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140456611,"alleles":["CCCC","CCC"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140456611,"alleles":["C","T"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456611,"clinical_significance":[],"seq_region_name":"7","id":"rs764442316"},{"clinical_significance":[],"id":"rs1794473153","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["AAAA","AA"],"end":140456615,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456612},{"alleles":["A","C"],"end":140456614,"strand":1,"feature_type":"variation","start":140456614,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","id":"rs751643168","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1395458147","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140456616,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456616},{"clinical_significance":[],"seq_region_name":"7","id":"rs927596154","source":"dbSNP","start":140456617,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140456617,"feature_type":"variation","strand":1},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456618,"feature_type":"variation","strand":1,"end":140456618,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794473404"},{"feature_type":"variation","strand":1,"end":140456621,"alleles":["A","T"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456621,"clinical_significance":[],"id":"rs1383234529","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563086211","source":"dbSNP","start":140456622,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140456622,"feature_type":"variation","strand":1},{"end":140456623,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140456623,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","id":"rs1423951412","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585463008","feature_type":"variation","strand":1,"end":140456635,"alleles":["C","T"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456635},{"feature_type":"variation","strand":1,"end":140456636,"alleles":["T","C"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456636,"clinical_significance":[],"seq_region_name":"7","id":"rs752388460"},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456639,"feature_type":"variation","strand":1,"end":140456639,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794473751"},{"seq_region_name":"7","id":"rs1398760858","clinical_significance":[],"start":140456643,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140456643,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"id":"rs1062771","seq_region_name":"7","clinical_significance":[],"start":140456654,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"stop_lost","alleles":["T","G"],"end":140456654,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1139716","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456656,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140456656},{"id":"rs1794474011","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140456662,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140456662},{"alleles":["G","C"],"end":140456674,"strand":1,"feature_type":"variation","start":140456674,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs1062770","clinical_significance":[]},{"seq_region_name":"7","id":"rs562305064","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140456675,"source":"dbSNP","strand":1,"feature_type":"variation","end":140456675,"alleles":["C","T"]},{"start":140456681,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140456681,"alleles":["A","G"],"strand":1,"feature_type":"variation","id":"rs757426959","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140456682,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140456682,"source":"dbSNP","seq_region_name":"7","id":"rs1794474326","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140456683,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140456683,"source":"dbSNP","seq_region_name":"7","id":"rs1333598995","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140456684,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140456684,"source":"dbSNP","id":"rs1794474457","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794474548","clinical_significance":[],"end":140456690,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140456690,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"seq_region_name":"7","id":"rs755599616","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140456691,"source":"dbSNP","strand":1,"feature_type":"variation","end":140456691,"alleles":["T","C"]},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456693,"feature_type":"variation","strand":1,"end":140456693,"alleles":["G","C"],"clinical_significance":[],"id":"rs1328488507","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140456694,"source":"dbSNP","strand":1,"feature_type":"variation","end":140456694,"alleles":["C","T"],"id":"rs1794474774","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140456695,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140456695,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1482074668"},{"alleles":["T","C"],"end":140456698,"feature_type":"variation","strand":1,"source":"dbSNP","start":140456698,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs781487298"},{"feature_type":"variation","strand":1,"end":140456699,"alleles":["G","A","C"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456699,"clinical_significance":[],"id":"rs749233455","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140456703,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140456703,"seq_region_name":"7","id":"rs1399982690","clinical_significance":[]},{"consequence_type":"stop_gained","assembly_name":"GRCh38","source":"dbSNP","start":140456705,"feature_type":"variation","strand":1,"end":140456705,"alleles":["G","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1313378671"},{"alleles":["C","T"],"end":140456709,"feature_type":"variation","strand":1,"source":"dbSNP","start":140456709,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794475297"},{"alleles":["T","A"],"end":140456712,"strand":1,"feature_type":"variation","start":140456712,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","id":"rs1062769","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs754920305","seq_region_name":"7","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456715,"feature_type":"variation","strand":1,"end":140456715,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1794475524","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140456717,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140456717,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140456721,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140456721,"source":"dbSNP","id":"rs778737482","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140456723,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140456723,"source":"dbSNP","seq_region_name":"7","id":"rs554245561","clinical_significance":[]},{"clinical_significance":[],"id":"rs747923133","seq_region_name":"7","alleles":["T","C"],"end":140456728,"feature_type":"variation","strand":1,"source":"dbSNP","start":140456728,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1585463208","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140456732,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456732},{"alleles":["G","A"],"end":140456734,"strand":1,"feature_type":"variation","start":140456734,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs1459792051","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1367179943","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140456735,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456735},{"seq_region_name":"7","id":"rs1794476057","clinical_significance":[],"start":140456737,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["T","C"],"end":140456737,"strand":1,"feature_type":"variation"},{"end":140456740,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140456740,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs771701754","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs772862496","source":"dbSNP","start":140456741,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140456741,"feature_type":"variation","strand":1},{"alleles":["C","T"],"end":140456745,"feature_type":"variation","strand":1,"source":"dbSNP","start":140456745,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs777207403","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140456746,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140456746,"source":"dbSNP","seq_region_name":"7","id":"rs746447217","clinical_significance":[]},{"end":140456747,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140456747,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs770425288","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1062768","source":"dbSNP","start":140456748,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140456748,"alleles":["C","G","T"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140456749,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140456749,"source":"dbSNP","seq_region_name":"7","id":"rs1241069779","clinical_significance":[]},{"seq_region_name":"7","id":"rs760069606","clinical_significance":[],"end":140456750,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140456750,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456753,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140456753,"clinical_significance":[],"seq_region_name":"7","id":"rs1062767"},{"seq_region_name":"7","id":"rs1062766","clinical_significance":[],"start":140456754,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["C","T"],"end":140456754,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140456757,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140456757,"source":"dbSNP","id":"rs1238318327","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140456759,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456759,"clinical_significance":[],"seq_region_name":"7","id":"rs1794477294"},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140456760,"source":"dbSNP","strand":1,"feature_type":"variation","end":140456760,"alleles":["T","G"],"seq_region_name":"7","id":"rs1585463367","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794477542","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140456763,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140456763},{"seq_region_name":"7","id":"rs1794477666","clinical_significance":[],"strand":1,"feature_type":"variation","end":140456765,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140456765,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140456772,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140456772,"source":"dbSNP","seq_region_name":"7","id":"rs765704006","clinical_significance":["uncertain significance"]},{"consequence_type":"stop_gained","assembly_name":"GRCh38","source":"dbSNP","start":140456776,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140456776,"clinical_significance":[],"seq_region_name":"7","id":"rs775884934"},{"end":140456778,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140456778,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs1794478059","clinical_significance":[]},{"id":"rs763250772","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140456779,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140456779},{"source":"dbSNP","start":140456780,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140456780,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs368646881"},{"feature_type":"variation","strand":1,"end":140456781,"alleles":["T","A"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456781,"clinical_significance":[],"seq_region_name":"7","id":"rs2130248151"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794478445","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140456784,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456784},{"clinical_significance":[],"seq_region_name":"7","id":"rs918275518","end":140456785,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140456785,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs990968415","source":"dbSNP","start":140456791,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140456791,"alleles":["T","C"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140456792,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140456792,"source":"dbSNP","seq_region_name":"7","id":"rs751825296","clinical_significance":[]},{"clinical_significance":[],"id":"rs372241410","seq_region_name":"7","end":140456798,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140456798,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs767682916","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140456801,"source":"dbSNP","strand":1,"feature_type":"variation","end":140456801,"alleles":["C","A"]},{"source":"dbSNP","start":140456802,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140456802,"alleles":["A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1062765"},{"source":"dbSNP","start":140456803,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140456803,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs750508198"},{"alleles":["T","G"],"end":140456805,"feature_type":"variation","strand":1,"source":"dbSNP","start":140456805,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794479127"},{"clinical_significance":[],"seq_region_name":"7","id":"rs754901191","feature_type":"variation","strand":1,"end":140456807,"alleles":["C","T"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456807},{"start":140456808,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140456808,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585463530","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140456809,"alleles":["T","C"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456809,"clinical_significance":[],"seq_region_name":"7","id":"rs986572780"},{"source":"dbSNP","start":140456810,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140456810,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs778733127","seq_region_name":"7"},{"end":140456814,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140456814,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs376798349","clinical_significance":["uncertain significance"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1277037459","feature_type":"variation","strand":1,"end":140456815,"alleles":["G","A"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456815},{"alleles":["C","A"],"end":140456816,"feature_type":"variation","strand":1,"source":"dbSNP","start":140456816,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":["uncertain significance"],"seq_region_name":"7","id":"rs758191085"},{"source":"dbSNP","start":140456821,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140456821,"feature_type":"variation","strand":1,"clinical_significance":["uncertain significance"],"id":"rs777615203","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140456822,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456822,"clinical_significance":[],"seq_region_name":"7","id":"rs1062764"},{"consequence_type":"stop_gained","assembly_name":"GRCh38","source":"dbSNP","start":140456829,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140456829,"clinical_significance":[],"seq_region_name":"7","id":"rs979257316"},{"feature_type":"variation","strand":1,"end":140456834,"alleles":["C","A","T"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456834,"clinical_significance":[],"seq_region_name":"7","id":"rs1794480025"},{"seq_region_name":"7","id":"rs1563086511","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140456835,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140456835,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1311605003","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140456842,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140456842,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140456843,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140456843,"source":"dbSNP","seq_region_name":"7","id":"rs1794480263","clinical_significance":[]},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456849,"feature_type":"variation","strand":1,"end":140456849,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1482830985"},{"end":140456855,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140456855,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs770623379","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs780652876","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456860,"feature_type":"variation","strand":1,"end":140456860,"alleles":["T","C"]},{"id":"rs1445212516","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140456864,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140456864,"source":"dbSNP"},{"clinical_significance":[],"id":"rs749797587","seq_region_name":"7","end":140456865,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140456865,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"id":"rs935264675","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"splice_region_variant","start":140456870,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140456870},{"seq_region_name":"7","id":"rs1481524013","clinical_significance":[],"start":140456872,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_region_variant","end":140456872,"alleles":["G","C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs577097233","consequence_type":"splice_polypyrimidine_tract_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456875,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140456875},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140456876,"assembly_name":"GRCh38","consequence_type":"splice_polypyrimidine_tract_variant","start":140456876,"source":"dbSNP","seq_region_name":"7","id":"rs933899165","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"splice_polypyrimidine_tract_variant","start":140456877,"source":"dbSNP","strand":1,"feature_type":"variation","end":140456877,"alleles":["T","C"],"seq_region_name":"7","id":"rs1429013751","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1454694743","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140456878,"consequence_type":"splice_polypyrimidine_tract_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456878},{"seq_region_name":"7","id":"rs1585463710","clinical_significance":[],"end":140456879,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140456879,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_polypyrimidine_tract_variant"},{"consequence_type":"splice_polypyrimidine_tract_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456883,"feature_type":"variation","strand":1,"end":140456883,"alleles":["G","A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794481258"},{"start":140456885,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140456885,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs775877265","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456889,"feature_type":"variation","strand":1,"alleles":["AA","A"],"end":140456890,"clinical_significance":[],"id":"rs1159879662","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1383368740","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140456890,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140456890},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140456892,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","G"],"end":140456892,"seq_region_name":"7","id":"rs763312333","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140456898,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140456898,"source":"dbSNP","seq_region_name":"7","id":"rs1188274055","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130248892","alleles":["C","G"],"end":140456899,"feature_type":"variation","strand":1,"source":"dbSNP","start":140456899,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["A","G"],"end":140456900,"feature_type":"variation","strand":1,"source":"dbSNP","start":140456900,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794481639"},{"seq_region_name":"7","id":"rs1297001063","clinical_significance":[],"start":140456904,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AT","-"],"end":140456905,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1051071387","seq_region_name":"7","alleles":["T","C"],"end":140456905,"feature_type":"variation","strand":1,"source":"dbSNP","start":140456905,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs769128038","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140456906,"feature_type":"variation","strand":1,"end":140456906,"alleles":["T","C"]},{"source":"dbSNP","start":140456910,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140456910,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs774904230"},{"alleles":["T","G"],"end":140456913,"strand":1,"feature_type":"variation","start":140456913,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1311382048","seq_region_name":"7","clinical_significance":[]},{"end":140456919,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140456919,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794482047","clinical_significance":[]},{"alleles":["G","A","C"],"end":140456923,"strand":1,"feature_type":"variation","start":140456923,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs78256678","clinical_significance":[]},{"alleles":["A","G"],"end":140456924,"strand":1,"feature_type":"variation","start":140456924,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1794482214","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140456929,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140456929,"seq_region_name":"7","id":"rs1209130997","clinical_significance":[]},{"start":140456938,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140456938,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794482273","clinical_significance":[]},{"alleles":["T","G"],"end":140456939,"feature_type":"variation","strand":1,"source":"dbSNP","start":140456939,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs755085869"},{"source":"dbSNP","start":140456941,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["CACA","CA"],"end":140456944,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794482420"},{"id":"rs1237981315","seq_region_name":"7","clinical_significance":[],"end":140456943,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140456943,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1288107722","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140456943,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CAGTCA","CA"],"end":140456948},{"strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140456944,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140456944,"source":"dbSNP","seq_region_name":"7","id":"rs1563086588","clinical_significance":[]},{"start":140456946,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140456946,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1353088895","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs779286510","end":140456948,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140456948,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140456953,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140456953,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1281989370","clinical_significance":[]},{"end":140456954,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140456954,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1275662276","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1491553529","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140456958,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["ATA","A"],"end":140456960},{"strand":1,"feature_type":"variation","end":140456959,"alleles":["T","TT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140456959,"source":"dbSNP","seq_region_name":"7","id":"rs576745848","clinical_significance":[]},{"id":"rs1794482961","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140456959,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140456959,"source":"dbSNP"},{"id":"rs1007010801","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140456962,"strand":1,"feature_type":"variation","start":140456962,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794483172","alleles":["G","T"],"end":140456968,"feature_type":"variation","strand":1,"source":"dbSNP","start":140456968,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1323359135","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140456969,"source":"dbSNP","strand":1,"feature_type":"variation","end":140456974,"alleles":["AAAAAA","AAAAAAA"]},{"seq_region_name":"7","id":"rs1794483301","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140456977,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140456977},{"start":140456989,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140456989,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs77526235","clinical_significance":[]},{"seq_region_name":"7","id":"rs1276601219","clinical_significance":[],"start":140456990,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140456990,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs572306848","clinical_significance":[],"alleles":["C","A","G","T"],"end":140456994,"strand":1,"feature_type":"variation","start":140456994,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs905983256","clinical_significance":[],"end":140456995,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140456995,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1417313669","seq_region_name":"7","clinical_significance":[],"start":140456998,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AATTAGCTTTGCTGACAAG","-"],"end":140457016,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140457000,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457000,"clinical_significance":[],"seq_region_name":"7","id":"rs1794483734"},{"seq_region_name":"7","id":"rs1379217287","clinical_significance":[],"strand":1,"feature_type":"variation","end":140457001,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457001,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140457002,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457002,"source":"dbSNP","id":"rs1794483866","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140457008,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140457008,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1794483930","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457011,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140457011,"seq_region_name":"7","id":"rs551344907","clinical_significance":[]},{"source":"dbSNP","start":140457013,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140457013,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1020561812"},{"seq_region_name":"7","id":"rs1412548650","clinical_significance":[],"start":140457014,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140457014,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457015,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140457015,"clinical_significance":[],"seq_region_name":"7","id":"rs1017125453"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457017,"source":"dbSNP","strand":1,"feature_type":"variation","end":140457017,"alleles":["T","A"],"id":"rs1585463939","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457021,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140457021,"seq_region_name":"7","id":"rs907477231","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794484343","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457023,"feature_type":"variation","strand":1,"end":140457023,"alleles":["C","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457028,"feature_type":"variation","strand":1,"end":140457028,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1563086645"},{"end":140457030,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140457030,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1488503418"},{"source":"dbSNP","start":140457031,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140457031,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs898640065"},{"start":140457031,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["GTGT","GT"],"end":140457034,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1402379898","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457033,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140457033,"clinical_significance":[],"id":"rs1794484628","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457033,"feature_type":"variation","strand":1,"end":140457033,"alleles":["G","-"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794484678"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457034,"source":"dbSNP","strand":1,"feature_type":"variation","end":140457034,"alleles":["T","G"],"seq_region_name":"7","id":"rs1585463987","clinical_significance":[]},{"seq_region_name":"7","id":"rs61226924","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457034,"source":"dbSNP","strand":1,"feature_type":"variation","end":140457043,"alleles":["TTTTTTTTTT","TTT","TTTTTT","TTTTTTT","TTTTTTTT","TTTTTTTTT","TTTTTTTTTTT","TTTTTTTTTTTT"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585464048","end":140457035,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140457035,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1585464050","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457039,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140457039},{"seq_region_name":"7","id":"rs1003124428","clinical_significance":[],"strand":1,"feature_type":"variation","end":140457047,"alleles":["TTTTTGTTT","TTT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457039,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457040,"source":"dbSNP","strand":1,"feature_type":"variation","end":140457040,"alleles":["T","C","G"],"seq_region_name":"7","id":"rs563167032","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["TTTTGTTT","TTT"],"end":140457047,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457040,"clinical_significance":[],"seq_region_name":"7","id":"rs1279036682"},{"clinical_significance":[],"id":"rs959263692","seq_region_name":"7","alleles":["-","G"],"end":140457040,"feature_type":"variation","strand":1,"source":"dbSNP","start":140457041,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs146223954","clinical_significance":[],"start":140457041,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140457055,"alleles":["TTTGTTTGTTTGTTT","TTTGTTTGTTT","TTTGTTTGTTTGTTTGTTT"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1443256707","alleles":["TTGTT","TT"],"end":140457046,"feature_type":"variation","strand":1,"source":"dbSNP","start":140457042,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1585464090","clinical_significance":[],"start":140457043,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140457043,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs201881699","source":"dbSNP","start":140457043,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TGT","T"],"end":140457045,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457044,"feature_type":"variation","strand":1,"end":140457044,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1235865276"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1017070492","feature_type":"variation","strand":1,"end":140457046,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457046},{"seq_region_name":"7","id":"rs1189782383","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457048,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140457048},{"end":140457051,"alleles":["TTT","TTTT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140457049,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1359311451","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794486283","alleles":["G","T"],"end":140457052,"feature_type":"variation","strand":1,"source":"dbSNP","start":140457052,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794486344","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457053,"feature_type":"variation","strand":1,"end":140457057,"alleles":["TTTTT","TTTTTT"]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140457059,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457059,"clinical_significance":[],"seq_region_name":"7","id":"rs560659561"},{"source":"dbSNP","start":140457060,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140457060,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs527655336"},{"seq_region_name":"7","id":"rs1794486550","clinical_significance":[],"end":140457061,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140457061,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1794486610","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140457062,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457062,"source":"dbSNP"},{"alleles":["G","A"],"end":140457063,"feature_type":"variation","strand":1,"source":"dbSNP","start":140457063,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794486664"},{"end":140457067,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140457067,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs530434859"},{"seq_region_name":"7","id":"rs1794486766","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457077,"source":"dbSNP","strand":1,"feature_type":"variation","end":140457077,"alleles":["C","T"]},{"strand":1,"feature_type":"variation","end":140457078,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457078,"source":"dbSNP","seq_region_name":"7","id":"rs955641359","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794486953","clinical_significance":[],"start":140457083,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140457083,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457085,"source":"dbSNP","strand":1,"feature_type":"variation","end":140457085,"alleles":["T","C"],"id":"rs1425586833","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140457092,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457092,"source":"dbSNP","seq_region_name":"7","id":"rs2130249945","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794487121","source":"dbSNP","start":140457093,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140457093,"alleles":["T","C"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140457099,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457099,"clinical_significance":[],"seq_region_name":"7","id":"rs1191389245"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794487336","feature_type":"variation","strand":1,"end":140457105,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457105},{"end":140457107,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140457107,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs918404050","clinical_significance":[]},{"source":"dbSNP","start":140457107,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140457107,"alleles":["C","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794487541"},{"source":"dbSNP","start":140457108,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140457108,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs140991189"},{"seq_region_name":"7","id":"rs1794487781","clinical_significance":[],"alleles":["G","A"],"end":140457110,"strand":1,"feature_type":"variation","start":140457110,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140457113,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457113,"clinical_significance":[],"id":"rs1794487883","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457128,"feature_type":"variation","strand":1,"end":140457128,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794487983"},{"clinical_significance":[],"id":"rs1794488076","seq_region_name":"7","alleles":["TTTT","TTT"],"end":140457132,"feature_type":"variation","strand":1,"source":"dbSNP","start":140457129,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794488162","source":"dbSNP","start":140457132,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140457132,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1212273599","clinical_significance":[],"start":140457135,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140457135,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140457136,"alleles":["T","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457136,"clinical_significance":[],"seq_region_name":"7","id":"rs1794488340"},{"seq_region_name":"7","id":"rs1017920081","clinical_significance":[],"start":140457137,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140457137,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140457138,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140457138,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130250145"},{"seq_region_name":"7","id":"rs1794488545","clinical_significance":[],"strand":1,"feature_type":"variation","end":140457139,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457139,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794488635","end":140457143,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140457143,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["AACCTGGAGCTCAAC","AAC"],"end":140457157,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457143,"clinical_significance":[],"id":"rs1404724864","seq_region_name":"7"},{"clinical_significance":[],"id":"rs911232236","seq_region_name":"7","feature_type":"variation","strand":1,"end":140457151,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457151},{"feature_type":"variation","strand":1,"end":140457154,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457154,"clinical_significance":[],"id":"rs1794488958","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140457161,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457161,"clinical_significance":[],"seq_region_name":"7","id":"rs942657176"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457165,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140457165,"clinical_significance":[],"seq_region_name":"7","id":"rs1794489164"},{"seq_region_name":"7","id":"rs1435138426","clinical_significance":[],"end":140457167,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140457167,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140457169,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140457169,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs963791398"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457170,"feature_type":"variation","strand":1,"end":140457170,"alleles":["G","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs190659838"},{"id":"rs1380463107","seq_region_name":"7","clinical_significance":[],"start":140457171,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140457171,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140457178,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140457178,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1286480322"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457181,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140457181,"id":"rs1794489751","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs893181372","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457182,"feature_type":"variation","strand":1,"end":140457182,"alleles":["T","G"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457184,"feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140457184,"clinical_significance":[],"seq_region_name":"7","id":"rs1794489919"},{"source":"dbSNP","start":140457186,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140457186,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1338262100"},{"start":140457189,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140457189,"alleles":["T","A"],"strand":1,"feature_type":"variation","id":"rs1794490112","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140457190,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457190,"source":"dbSNP","id":"rs925137870","seq_region_name":"7","clinical_significance":[]},{"start":140457191,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140457191,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs1335662150","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794490366","clinical_significance":[],"strand":1,"feature_type":"variation","end":140457193,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457193,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1465865432","clinical_significance":[],"start":140457200,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140457200,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794490526","alleles":["A","G"],"end":140457205,"feature_type":"variation","strand":1,"source":"dbSNP","start":140457205,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794490607","source":"dbSNP","start":140457207,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140457207,"alleles":["G","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs747290317","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457210,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C","T"],"end":140457210},{"start":140457211,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140457211,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1464929918","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["TT","T"],"end":140457212,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457211,"source":"dbSNP","seq_region_name":"7","id":"rs1168223982","clinical_significance":[]},{"seq_region_name":"7","id":"rs1414366996","clinical_significance":[],"end":140457215,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140457215,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140457217,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457217,"clinical_significance":[],"id":"rs375369335","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1237026396","clinical_significance":[],"alleles":["T","C"],"end":140457224,"strand":1,"feature_type":"variation","start":140457224,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["T","A"],"end":140457231,"feature_type":"variation","strand":1,"source":"dbSNP","start":140457231,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1794491287","seq_region_name":"7"},{"seq_region_name":"7","id":"rs552104862","clinical_significance":[],"alleles":["C","A","G","T"],"end":140457234,"strand":1,"feature_type":"variation","start":140457234,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140457235,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140457235,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1459225161","clinical_significance":[]},{"seq_region_name":"7","id":"rs907361409","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140457236,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457236,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140457237,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457237,"clinical_significance":[],"seq_region_name":"7","id":"rs532070426"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794491590","alleles":["A","C"],"end":140457239,"feature_type":"variation","strand":1,"source":"dbSNP","start":140457239,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1046172664","feature_type":"variation","strand":1,"end":140457240,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457240},{"seq_region_name":"7","id":"rs1292641552","clinical_significance":[],"start":140457242,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140457242,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457243,"feature_type":"variation","strand":1,"alleles":["A","C","G","T"],"end":140457243,"clinical_significance":[],"seq_region_name":"7","id":"rs1003134173"},{"start":140457244,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140457244,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1202413405","clinical_significance":[]},{"seq_region_name":"7","id":"rs1034559969","clinical_significance":[],"start":140457246,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C"],"end":140457246,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457250,"source":"dbSNP","strand":1,"feature_type":"variation","end":140457250,"alleles":["C","T"],"seq_region_name":"7","id":"rs550069835","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1378594976","feature_type":"variation","strand":1,"end":140457254,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457254},{"alleles":["A","T"],"end":140457255,"strand":1,"feature_type":"variation","start":140457255,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs937424121","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140457256,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457256,"source":"dbSNP","seq_region_name":"7","id":"rs1460954632","clinical_significance":[]},{"end":140457257,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140457257,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1350310397","clinical_significance":[]},{"end":140457262,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140457262,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs116245645","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1209384820","alleles":["CTCTCT","CTCT"],"end":140457267,"feature_type":"variation","strand":1,"source":"dbSNP","start":140457262,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457263,"source":"dbSNP","strand":1,"feature_type":"variation","end":140457263,"alleles":["T","C"],"id":"rs1448272195","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140457264,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457264,"source":"dbSNP","id":"rs1794493086","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1016584752","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457265,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140457265},{"source":"dbSNP","start":140457266,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140457266,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs762894498"},{"seq_region_name":"7","id":"rs1563086805","clinical_significance":[],"start":140457272,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140457272,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1441635500","clinical_significance":[],"end":140457273,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140457273,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140457276,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140457276,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794493573","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457278,"feature_type":"variation","strand":1,"end":140457278,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1378586291"},{"id":"rs1794493741","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140457280,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457280,"source":"dbSNP"},{"end":140457285,"alleles":["AAAAA","AAAA","AAAAAA"],"strand":1,"feature_type":"variation","start":140457281,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs962802499","clinical_significance":[]},{"seq_region_name":"7","id":"rs898671245","clinical_significance":[],"end":140457283,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140457283,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457294,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140457294,"seq_region_name":"7","id":"rs1479171141","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs972457111","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457295,"feature_type":"variation","strand":1,"end":140457295,"alleles":["C","T"]},{"source":"dbSNP","start":140457300,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140457300,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs752991516"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794494427","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140457301,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457301},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794494512","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140457312,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457312},{"clinical_significance":[],"seq_region_name":"7","id":"rs1219971975","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457313,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140457313},{"seq_region_name":"7","id":"rs1794494663","clinical_significance":[],"strand":1,"feature_type":"variation","end":140457316,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457316,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1428102237","seq_region_name":"7","feature_type":"variation","strand":1,"end":140457317,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457317},{"source":"dbSNP","start":140457321,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140457321,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1451498352","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140457325,"alleles":["C","A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457325,"source":"dbSNP","seq_region_name":"7","id":"rs1457419462","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1025467799","alleles":["T","A"],"end":140457326,"feature_type":"variation","strand":1,"source":"dbSNP","start":140457326,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1025807383","clinical_significance":[],"start":140457327,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140457327,"strand":1,"feature_type":"variation"},{"id":"rs1794497873","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140457330,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457330,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["CACAC","CAC"],"end":140457335,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457331,"source":"dbSNP","seq_region_name":"7","id":"rs1355237548","clinical_significance":[]},{"seq_region_name":"7","id":"rs1322014811","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140457335,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457335,"source":"dbSNP"},{"start":140457340,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140457340,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","id":"rs955175932","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457345,"feature_type":"variation","strand":1,"end":140457345,"alleles":["G","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1222896764"},{"end":140457349,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140457349,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1367998087","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1381640047","alleles":["C","T"],"end":140457356,"feature_type":"variation","strand":1,"source":"dbSNP","start":140457356,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs986683476","seq_region_name":"7","clinical_significance":[],"start":140457358,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","AA"],"end":140457358,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457359,"source":"dbSNP","strand":1,"feature_type":"variation","end":140457359,"alleles":["C","T"],"id":"rs911106958","seq_region_name":"7","clinical_significance":[]},{"id":"rs1364824521","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140457360,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457360,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140457361,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457361,"source":"dbSNP","seq_region_name":"7","id":"rs1298736412","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140457362,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457362,"clinical_significance":[],"seq_region_name":"7","id":"rs1313763511"},{"start":140457365,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140457365,"strand":1,"feature_type":"variation","id":"rs891393908","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794498684","clinical_significance":[],"start":140457366,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140457366,"alleles":["G","A","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1008466154","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457377,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140457377},{"seq_region_name":"7","id":"rs1794498860","clinical_significance":[],"end":140457381,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140457381,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["C","T"],"end":140457382,"strand":1,"feature_type":"variation","start":140457382,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794498954","clinical_significance":[]},{"end":140457389,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140457389,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1324065754","clinical_significance":[]},{"source":"dbSNP","start":140457391,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140457391,"alleles":["A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs371144116"},{"start":140457394,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140457394,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794499323","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140457398,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457398,"source":"dbSNP","seq_region_name":"7","id":"rs1158629748","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140457399,"alleles":["G","C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457399,"clinical_significance":[],"seq_region_name":"7","id":"rs942730324"},{"alleles":["T","C"],"end":140457400,"strand":1,"feature_type":"variation","start":140457400,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794499618","clinical_significance":[]},{"source":"dbSNP","start":140457403,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140457403,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1018371202"},{"clinical_significance":[],"id":"rs1427570551","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457411,"feature_type":"variation","strand":1,"end":140457411,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1189798182","clinical_significance":[],"end":140457413,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140457413,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1794499925","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140457414,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457414,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1477914806","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457416,"feature_type":"variation","strand":1,"end":140457416,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794500056","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457417,"feature_type":"variation","strand":1,"end":140457417,"alleles":["A","C"]},{"seq_region_name":"7","id":"rs990585689","clinical_significance":[],"start":140457418,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140457418,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"alleles":["T","A","C"],"end":140457420,"feature_type":"variation","strand":1,"source":"dbSNP","start":140457420,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1230742454","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1273322816","end":140457421,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140457421,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs914576267","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140457423,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457423},{"clinical_significance":[],"seq_region_name":"7","id":"rs946147502","feature_type":"variation","strand":1,"end":140457425,"alleles":["T","A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457425},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457426,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140457426,"seq_region_name":"7","id":"rs1794500521","clinical_significance":[]},{"id":"rs1794500585","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140457428,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457428,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1283304969","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457429,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140457429},{"seq_region_name":"7","id":"rs1794500697","clinical_significance":[],"strand":1,"feature_type":"variation","end":140457431,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457431,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1794500760","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457435,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140457435},{"source":"dbSNP","start":140457437,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140457437,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1041789159"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457441,"feature_type":"variation","strand":1,"end":140457441,"alleles":["A","C"],"clinical_significance":[],"id":"rs907372542","seq_region_name":"7"},{"end":140457442,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140457442,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs938806862","seq_region_name":"7"},{"seq_region_name":"7","id":"rs2130251795","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140457452,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457452,"source":"dbSNP"},{"clinical_significance":[],"id":"rs2130251815","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140457453,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457453},{"end":140457458,"alleles":["AAACA","-"],"strand":1,"feature_type":"variation","start":140457454,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1229213288","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457454,"feature_type":"variation","strand":1,"end":140457464,"alleles":["AAACATAAAAA","-"],"clinical_significance":[],"seq_region_name":"7","id":"rs572604211"},{"start":140457454,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AAACATAAAAATGCAGAAAAC","AAAC"],"end":140457474,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1217194686","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1344711155","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457456,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140457456},{"clinical_significance":[],"id":"rs1278752374","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["AAAAA","AAAAAA"],"end":140457464,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457460},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457460,"source":"dbSNP","strand":1,"feature_type":"variation","end":140457473,"alleles":["AAAAATGCAGAAAA","AA"],"seq_region_name":"7","id":"rs1270157910","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140457461,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457461,"source":"dbSNP","seq_region_name":"7","id":"rs1794501392","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140457471,"alleles":["GCAGAA","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457466,"source":"dbSNP","seq_region_name":"7","id":"rs552761221","clinical_significance":[]},{"end":140457469,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140457469,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1401822308","clinical_significance":[]},{"id":"rs963658749","seq_region_name":"7","clinical_significance":[],"end":140457471,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140457471,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794501653","source":"dbSNP","start":140457475,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140457475,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1463554579","end":140457479,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140457479,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140457484,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140457486,"alleles":["TTT","TTTT"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794501768"},{"source":"dbSNP","start":140457485,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C","G"],"end":140457485,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs979155678","seq_region_name":"7"},{"start":140457489,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140457489,"alleles":["A","G"],"strand":1,"feature_type":"variation","id":"rs1794501990","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457493,"feature_type":"variation","strand":1,"end":140457493,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1361057620"},{"strand":1,"feature_type":"variation","end":140457497,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457497,"source":"dbSNP","seq_region_name":"7","id":"rs1174231861","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140457499,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457499,"clinical_significance":[],"seq_region_name":"7","id":"rs1205064296"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457503,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140457503,"seq_region_name":"7","id":"rs1794502245","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1424846006","feature_type":"variation","strand":1,"end":140457506,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457506},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457512,"feature_type":"variation","strand":1,"end":140457512,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs766253556"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794502458","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457513,"feature_type":"variation","strand":1,"end":140457513,"alleles":["T","C"]},{"feature_type":"variation","strand":1,"end":140457517,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457517,"clinical_significance":[],"seq_region_name":"7","id":"rs1794502516"},{"clinical_significance":[],"id":"rs1453705392","seq_region_name":"7","source":"dbSNP","start":140457518,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140457518,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794502647","source":"dbSNP","start":140457521,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140457521,"alleles":["G","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1794502704","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457522,"source":"dbSNP","strand":1,"feature_type":"variation","end":140457522,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1585464779","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140457524,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457524,"source":"dbSNP"},{"start":140457525,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140457525,"alleles":["T","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1056069656","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457526,"source":"dbSNP","strand":1,"feature_type":"variation","end":140457526,"alleles":["T","A"],"seq_region_name":"7","id":"rs894745381","clinical_significance":[]},{"seq_region_name":"7","id":"rs1483292977","clinical_significance":[],"start":140457527,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140457527,"alleles":["C","G","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs535672794","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140457528,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457528,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457530,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140457530,"seq_region_name":"7","id":"rs1585464806","clinical_significance":[]},{"alleles":["C","A"],"end":140457532,"feature_type":"variation","strand":1,"source":"dbSNP","start":140457532,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1207660640"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794503238","end":140457533,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140457533,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["A","G"],"end":140457534,"feature_type":"variation","strand":1,"source":"dbSNP","start":140457534,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1794503330","seq_region_name":"7"},{"alleles":["T","C"],"end":140457538,"strand":1,"feature_type":"variation","start":140457538,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794503399","clinical_significance":[]},{"alleles":["G","A","C"],"end":140457539,"feature_type":"variation","strand":1,"source":"dbSNP","start":140457539,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1322536593"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794503541","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457540,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140457540},{"seq_region_name":"7","id":"rs1794503595","clinical_significance":[],"start":140457549,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140457549,"strand":1,"feature_type":"variation"},{"start":140457550,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","T"],"end":140457550,"strand":1,"feature_type":"variation","id":"rs144928785","seq_region_name":"7","clinical_significance":[]},{"end":140457551,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140457551,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1268582055"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1038484699","end":140457555,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140457555,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794503897","source":"dbSNP","start":140457559,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140457559,"alleles":["A","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1381521767","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140457565,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457565},{"strand":1,"feature_type":"variation","alleles":["AAAAA","AAA"],"end":140457572,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457568,"source":"dbSNP","seq_region_name":"7","id":"rs2130252468","clinical_significance":[]},{"clinical_significance":[],"id":"rs1794504010","seq_region_name":"7","source":"dbSNP","start":140457572,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140457572,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457573,"source":"dbSNP","strand":1,"feature_type":"variation","end":140457573,"alleles":["T","C"],"seq_region_name":"7","id":"rs1794504067","clinical_significance":[]},{"seq_region_name":"7","id":"rs1301292506","clinical_significance":[],"end":140457574,"alleles":["A","AA"],"strand":1,"feature_type":"variation","start":140457574,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1794504182","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457576,"source":"dbSNP","strand":1,"feature_type":"variation","end":140457576,"alleles":["A","G"]},{"clinical_significance":[],"id":"rs993887523","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140457581,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457581},{"seq_region_name":"7","id":"rs1401338057","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457588,"source":"dbSNP","strand":1,"feature_type":"variation","end":140457588,"alleles":["G","A","C"]},{"alleles":["G","A"],"end":140457591,"feature_type":"variation","strand":1,"source":"dbSNP","start":140457591,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1160912600"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794504457","source":"dbSNP","start":140457594,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140457594,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1794504515","clinical_significance":[],"alleles":["GG","G"],"end":140457597,"strand":1,"feature_type":"variation","start":140457596,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs373884794","clinical_significance":[],"end":140457597,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140457597,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1372941371","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457601,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140457601},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794504690","source":"dbSNP","start":140457602,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140457602,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1166192722","end":140457605,"alleles":["CC","CCC"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140457604,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457611,"source":"dbSNP","strand":1,"feature_type":"variation","end":140457611,"alleles":["T","C"],"seq_region_name":"7","id":"rs1794504795","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457612,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140457612,"clinical_significance":[],"seq_region_name":"7","id":"rs1423874079"},{"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140457613,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457613,"source":"dbSNP","id":"rs1025310993","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs917743141","clinical_significance":[],"start":140457618,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140457618,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140457622,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457622,"clinical_significance":[],"id":"rs1452353622","seq_region_name":"7"},{"source":"dbSNP","start":140457623,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140457623,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs774158417"},{"seq_region_name":"7","id":"rs955227545","clinical_significance":[],"end":140457624,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140457624,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1794505242","seq_region_name":"7","feature_type":"variation","strand":1,"end":140457625,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457625},{"end":140457629,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140457629,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1794505290","seq_region_name":"7"},{"alleles":["G","A"],"end":140457633,"feature_type":"variation","strand":1,"source":"dbSNP","start":140457633,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1007988555"},{"strand":1,"feature_type":"variation","alleles":["CTGCAGTGAGCCGAGACTGCA","CTGCAGTGAGCCGAGACTGCAGTGAGCCGAGACTGCA"],"end":140457655,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457635,"source":"dbSNP","id":"rs1163805195","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794505478","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457637,"feature_type":"variation","strand":1,"end":140457637,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585464961","feature_type":"variation","strand":1,"end":140457641,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457641},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457642,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140457642,"seq_region_name":"7","id":"rs980688619","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs566594967","source":"dbSNP","start":140457644,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140457644,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794505673","source":"dbSNP","start":140457646,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140457646,"alleles":["C","A","T"],"feature_type":"variation","strand":1},{"id":"rs147551531","seq_region_name":"7","clinical_significance":[],"start":140457647,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140457647,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs964330264","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140457652,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457652,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1794505894","clinical_significance":[],"end":140457659,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140457659,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140457661,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140457661,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794505972"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457663,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140457663,"clinical_significance":[],"seq_region_name":"7","id":"rs1794506072"},{"id":"rs1323546156","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457664,"source":"dbSNP","strand":1,"feature_type":"variation","end":140457664,"alleles":["C","T"]},{"end":140457667,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140457667,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1794506172","seq_region_name":"7"},{"end":140457668,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140457668,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1384985000","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794506294","clinical_significance":[],"strand":1,"feature_type":"variation","end":140457669,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457669,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457670,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140457670,"seq_region_name":"7","id":"rs1310611724","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1452030206","feature_type":"variation","strand":1,"end":140457674,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457674},{"seq_region_name":"7","id":"rs1794506470","clinical_significance":[],"end":140457675,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140457675,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1302354619","source":"dbSNP","start":140457676,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140457676,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457677,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140457677,"id":"rs1794506602","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457679,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140457679,"seq_region_name":"7","id":"rs1333620562","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794506740","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","CC"],"end":140457679,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457679,"source":"dbSNP"},{"end":140457682,"alleles":["AAA","AAAAA"],"strand":1,"feature_type":"variation","start":140457680,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1445018344","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457681,"source":"dbSNP","strand":1,"feature_type":"variation","end":140457687,"alleles":["AAGCAAG","AAG"],"id":"rs1396298819","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["CTCT","CT"],"end":140457692,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457689,"clinical_significance":[],"seq_region_name":"7","id":"rs1164322557"},{"end":140457690,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140457690,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1350870161","clinical_significance":[]},{"id":"rs1410681018","seq_region_name":"7","clinical_significance":[],"start":140457691,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140457691,"alleles":["C","A","G"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457696,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140457696,"seq_region_name":"7","id":"rs1585465051","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457697,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140457697,"seq_region_name":"7","id":"rs1794507123","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140457706,"alleles":["AAAAAAAAA","AAAAAAAA","AAAAAAAAAA","AAAAAAAAAAA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457698,"clinical_significance":[],"seq_region_name":"7","id":"rs756112935"},{"clinical_significance":[],"id":"rs759298331","seq_region_name":"7","source":"dbSNP","start":140457701,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140457701,"alleles":["A","G","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs200204912","feature_type":"variation","strand":1,"alleles":["AAAAATAAAAATAAAAA","AAAAATAAAAA"],"end":140457718,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457702},{"seq_region_name":"7","id":"rs1794507485","clinical_significance":[],"start":140457706,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140457706,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"end":140457707,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","start":140457707,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1238354409","clinical_significance":[]},{"seq_region_name":"7","id":"rs1435855313","clinical_significance":[],"end":140457710,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140457710,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1249601983","seq_region_name":"7","clinical_significance":[],"start":140457713,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140457713,"alleles":["T","A","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs914565341","clinical_significance":[],"alleles":["AAAAAAAA","AA","AAAAAAA","AAAAAAAAA"],"end":140457721,"strand":1,"feature_type":"variation","start":140457714,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140457718,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140457718,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1647710647"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1289515408","source":"dbSNP","start":140457719,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140457719,"alleles":["A","T"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457721,"source":"dbSNP","strand":1,"feature_type":"variation","end":140457721,"alleles":["A","G","T"],"seq_region_name":"7","id":"rs1038370330","clinical_significance":[]},{"id":"rs1266083659","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140457722,"alleles":["T","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457722,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585465130","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457724,"feature_type":"variation","strand":1,"end":140457727,"alleles":["ACAC","AC"]},{"seq_region_name":"7","id":"rs1794508146","clinical_significance":[],"strand":1,"feature_type":"variation","end":140457725,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457725,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1354588224","clinical_significance":[],"start":140457726,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140457726,"alleles":["A","C","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1311721614","alleles":["C","T"],"end":140457730,"feature_type":"variation","strand":1,"source":"dbSNP","start":140457730,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140457732,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C","T"],"end":140457732,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794508345"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457735,"feature_type":"variation","strand":1,"end":140457735,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs967332011"},{"seq_region_name":"7","id":"rs977520359","clinical_significance":[],"start":140457738,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140457738,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1324575177","clinical_significance":[],"end":140457741,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140457741,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1388911149","clinical_significance":[],"alleles":["C","T"],"end":140457744,"strand":1,"feature_type":"variation","start":140457744,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457752,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140457752,"id":"rs928672761","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140457756,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457756,"source":"dbSNP","seq_region_name":"7","id":"rs920046672","clinical_significance":[]},{"clinical_significance":[],"id":"rs1389134766","seq_region_name":"7","alleles":["CATCATCA","CATCA"],"end":140457765,"feature_type":"variation","strand":1,"source":"dbSNP","start":140457758,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457762,"source":"dbSNP","strand":1,"feature_type":"variation","end":140457762,"alleles":["A","G"],"seq_region_name":"7","id":"rs1303088310","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs938734606","source":"dbSNP","start":140457768,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C","G"],"end":140457768,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1794508992","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457768,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AAA","AAAA"],"end":140457770},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140457769,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457769,"source":"dbSNP","seq_region_name":"7","id":"rs1160065277","clinical_significance":[]},{"id":"rs1468245697","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140457770,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457770,"source":"dbSNP"},{"alleles":["A","G"],"end":140457772,"feature_type":"variation","strand":1,"source":"dbSNP","start":140457772,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1056387842"},{"id":"rs1208570825","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140457778,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457778,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1794509447","clinical_significance":[],"alleles":["C","T"],"end":140457781,"strand":1,"feature_type":"variation","start":140457781,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140457784,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457784,"source":"dbSNP","id":"rs1434688429","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs916081323","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140457786,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457786,"source":"dbSNP"},{"end":140457794,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140457794,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794509636"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585465253","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140457797,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457797},{"seq_region_name":"7","id":"rs10715334","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457797,"source":"dbSNP","strand":1,"feature_type":"variation","end":140457802,"alleles":["AAAAAA","AAAAA","AAAAAAA"]},{"id":"rs80210262","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457801,"source":"dbSNP","strand":1,"feature_type":"variation","end":140457801,"alleles":["A","C"]},{"seq_region_name":"7","id":"rs74457042","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457803,"source":"dbSNP","strand":1,"feature_type":"variation","end":140457803,"alleles":["C","T"]},{"start":140457804,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140457804,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs558571319","clinical_significance":[]},{"clinical_significance":[],"id":"rs1488644550","seq_region_name":"7","end":140457810,"alleles":["ATATATA","ATATA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140457804,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140457809,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140457809,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs930056800"},{"seq_region_name":"7","id":"rs1794510196","clinical_significance":[],"start":140457811,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140457811,"strand":1,"feature_type":"variation"},{"start":140457813,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140457813,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs142000104","clinical_significance":[]},{"source":"dbSNP","start":140457817,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140457817,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1350165384"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457819,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140457819,"clinical_significance":[],"seq_region_name":"7","id":"rs1794510299"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794510355","source":"dbSNP","start":140457825,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140457825,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1249117353","source":"dbSNP","start":140457827,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140457827,"alleles":["G","C"],"feature_type":"variation","strand":1},{"id":"rs752334879","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457833,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140457833},{"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140457837,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457837,"source":"dbSNP","seq_region_name":"7","id":"rs62490432","clinical_significance":[]},{"clinical_significance":[],"id":"rs1794510648","seq_region_name":"7","source":"dbSNP","start":140457841,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AATA","-"],"end":140457844,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs376218282","source":"dbSNP","start":140457842,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140457842,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794510795","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457842,"feature_type":"variation","strand":1,"end":140457848,"alleles":["ATATATA","ATATA"]},{"seq_region_name":"7","id":"rs1794510861","clinical_significance":[],"strand":1,"feature_type":"variation","end":140457854,"alleles":["ATATAGATATA","ATATA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457844,"source":"dbSNP"},{"id":"rs891265819","seq_region_name":"7","clinical_significance":[],"start":140457847,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140457847,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140457849,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457849,"clinical_significance":[],"seq_region_name":"7","id":"rs1344099041"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794511081","source":"dbSNP","start":140457850,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140457854,"alleles":["ATATA","ATA"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs182904409","alleles":["T","C"],"end":140457851,"feature_type":"variation","strand":1,"source":"dbSNP","start":140457851,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140457853,"alleles":["T","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457853,"source":"dbSNP","seq_region_name":"7","id":"rs1039892959","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457854,"feature_type":"variation","strand":1,"alleles":["AA","AAAA"],"end":140457855,"clinical_significance":[],"id":"rs534680293","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1369664003","source":"dbSNP","start":140457856,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140457856,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1363034948","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457857,"feature_type":"variation","strand":1,"end":140457857,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1299441911","source":"dbSNP","start":140457858,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140457861,"alleles":["TATA","TA"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs899517393","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457860,"feature_type":"variation","strand":1,"end":140457860,"alleles":["T","C"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457869,"source":"dbSNP","strand":1,"feature_type":"variation","end":140457869,"alleles":["A","C"],"seq_region_name":"7","id":"rs1383707089","clinical_significance":[]},{"source":"dbSNP","start":140457870,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140457870,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1172868379","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1000521394","clinical_significance":[],"strand":1,"feature_type":"variation","end":140457872,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457872,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457873,"source":"dbSNP","strand":1,"feature_type":"variation","end":140457873,"alleles":["T","C"],"id":"rs1456391186","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794511792","clinical_significance":[],"end":140457875,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140457875,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457876,"feature_type":"variation","strand":1,"end":140457876,"alleles":["C","G","T"],"clinical_significance":[],"id":"rs1585465380","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457886,"feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140457886,"clinical_significance":[],"seq_region_name":"7","id":"rs1198560353"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457887,"source":"dbSNP","strand":1,"feature_type":"variation","end":140457887,"alleles":["A","G"],"seq_region_name":"7","id":"rs1046813018","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457890,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140457890,"seq_region_name":"7","id":"rs1794512062","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs890904424","alleles":["T","C"],"end":140457891,"feature_type":"variation","strand":1,"source":"dbSNP","start":140457891,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs556502085","feature_type":"variation","strand":1,"end":140457893,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457893},{"clinical_significance":[],"seq_region_name":"7","id":"rs1279599833","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457894,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140457894},{"end":140457897,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140457897,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs546273624"},{"clinical_significance":[],"id":"rs1321829111","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457898,"feature_type":"variation","strand":1,"end":140457899,"alleles":["AA","AAA"]},{"start":140457899,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140457899,"alleles":["A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585465441","clinical_significance":[]},{"end":140457902,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140457902,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1219653592","seq_region_name":"7"},{"start":140457902,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140457926,"alleles":["TAGGGATCAAATTATGTCTACCTTA","TA"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794512634","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794512702","source":"dbSNP","start":140457906,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140457906,"alleles":["G","A"],"feature_type":"variation","strand":1},{"alleles":["T","G"],"end":140457913,"feature_type":"variation","strand":1,"source":"dbSNP","start":140457913,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1794512769","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457917,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140457917,"clinical_significance":[],"id":"rs956480162","seq_region_name":"7"},{"end":140457918,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140457918,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1268934815"},{"seq_region_name":"7","id":"rs1428030558","clinical_significance":[],"strand":1,"feature_type":"variation","end":140457921,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457921,"source":"dbSNP"},{"start":140457922,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G","T"],"end":140457922,"strand":1,"feature_type":"variation","id":"rs1018558123","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140457926,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457926,"clinical_significance":[],"seq_region_name":"7","id":"rs376262628"},{"end":140457930,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140457930,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794513139"},{"clinical_significance":[],"id":"rs1794513192","seq_region_name":"7","source":"dbSNP","start":140457931,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140457931,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs963878018","clinical_significance":[],"strand":1,"feature_type":"variation","end":140457932,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457932,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457933,"source":"dbSNP","strand":1,"feature_type":"variation","end":140457933,"alleles":["G","A"],"seq_region_name":"7","id":"rs1310111101","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794513370","feature_type":"variation","strand":1,"alleles":["CACAC","CAC"],"end":140457941,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457937},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140457939,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457939,"source":"dbSNP","seq_region_name":"7","id":"rs1794513439","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140457940,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457940,"source":"dbSNP","id":"rs2130254346","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585465497","end":140457941,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140457941,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794513558","source":"dbSNP","start":140457942,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140457942,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1403483854","alleles":["C","G"],"end":140457943,"feature_type":"variation","strand":1,"source":"dbSNP","start":140457943,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140457949,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140457949,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794513667","clinical_significance":[]},{"source":"dbSNP","start":140457950,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140457950,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1794513729","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1371508233","feature_type":"variation","strand":1,"alleles":["ATTTAAAAAGATGGAAATTTAAAA","ATTTAAAA"],"end":140457976,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457953},{"clinical_significance":[],"seq_region_name":"7","id":"rs59095120","source":"dbSNP","start":140457954,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140457956,"alleles":["TTT","TT"],"feature_type":"variation","strand":1},{"alleles":["-","G"],"end":140457960,"strand":1,"feature_type":"variation","start":140457961,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794513781","clinical_significance":[]},{"start":140457966,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140457966,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1011909815","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794513896","feature_type":"variation","strand":1,"alleles":["AAAA","AAA"],"end":140457976,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457973},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140457978,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457978,"source":"dbSNP","seq_region_name":"7","id":"rs1166160611","clinical_significance":[]},{"source":"dbSNP","start":140457980,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140457980,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1009307511"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1475120695","source":"dbSNP","start":140457981,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140457981,"alleles":["T","C"],"feature_type":"variation","strand":1},{"end":140457983,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140457983,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585465548"},{"seq_region_name":"7","id":"rs1794514167","clinical_significance":[],"start":140457986,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140457986,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1238175467","clinical_significance":[],"start":140457986,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["ATGAT","AT"],"end":140457990,"strand":1,"feature_type":"variation"},{"id":"rs1794514291","seq_region_name":"7","clinical_significance":[],"end":140457987,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140457987,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140457988,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140457988,"source":"dbSNP","seq_region_name":"7","id":"rs763600846","clinical_significance":[]},{"clinical_significance":[],"id":"rs1021518101","seq_region_name":"7","alleles":["T","C","G"],"end":140457991,"feature_type":"variation","strand":1,"source":"dbSNP","start":140457991,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457992,"feature_type":"variation","strand":1,"end":140457992,"alleles":["A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130254599"},{"id":"rs2130254619","seq_region_name":"7","clinical_significance":[],"start":140457994,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140457994,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1460108687","feature_type":"variation","strand":1,"end":140457998,"alleles":["A","C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140457998},{"seq_region_name":"7","id":"rs1794514551","clinical_significance":[],"start":140458001,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140458001,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140458004,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458004,"source":"dbSNP","id":"rs1794514611","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794514669","clinical_significance":[],"strand":1,"feature_type":"variation","end":140458007,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458007,"source":"dbSNP"},{"source":"dbSNP","start":140458010,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140458011,"alleles":["AA","AAA"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794514722"},{"clinical_significance":[],"id":"rs142112118","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458012,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140458012},{"alleles":["TAAAGTTAAAGTT","TAAAGTT"],"end":140458024,"feature_type":"variation","strand":1,"source":"dbSNP","start":140458012,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1313611118"},{"start":140458013,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140458013,"strand":1,"feature_type":"variation","id":"rs1199586889","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458014,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140458014,"clinical_significance":[],"id":"rs1794514982","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1794515047","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458015,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140458015},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140458019,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458019,"clinical_significance":[],"seq_region_name":"7","id":"rs757741046"},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140458020,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458020,"clinical_significance":[],"seq_region_name":"7","id":"rs1271486457"},{"id":"rs970545945","seq_region_name":"7","clinical_significance":[],"end":140458027,"alleles":["T","C","G"],"strand":1,"feature_type":"variation","start":140458027,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs6464779","seq_region_name":"7","source":"dbSNP","start":140458030,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140458030,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458032,"feature_type":"variation","strand":1,"end":140458032,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1454139810"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458033,"feature_type":"variation","strand":1,"end":140458033,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1563087202"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458037,"feature_type":"variation","strand":1,"end":140458037,"alleles":["T","C"],"clinical_significance":[],"id":"rs1291611819","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs960148741","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458046,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140458046},{"alleles":["T","C"],"end":140458048,"strand":1,"feature_type":"variation","start":140458048,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794515612","clinical_significance":[]},{"end":140458051,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140458051,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130254858"},{"id":"rs1794515673","seq_region_name":"7","clinical_significance":[],"start":140458054,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140458054,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"start":140458056,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140458056,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1343360085","clinical_significance":[]},{"start":140458060,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["CATACAC","C"],"end":140458066,"strand":1,"feature_type":"variation","id":"rs1207682726","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140458061,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458061,"source":"dbSNP","id":"rs1272904509","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140458062,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458062,"source":"dbSNP","seq_region_name":"7","id":"rs1794515924","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140458064,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458064,"source":"dbSNP","seq_region_name":"7","id":"rs926559683","clinical_significance":[]},{"alleles":["G","T"],"end":140458071,"feature_type":"variation","strand":1,"source":"dbSNP","start":140458071,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794516060"},{"seq_region_name":"7","id":"rs1356125609","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458075,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140458075},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794516159","end":140458077,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140458077,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794516208","feature_type":"variation","strand":1,"end":140458079,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458079},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458086,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140458086,"clinical_significance":[],"seq_region_name":"7","id":"rs1585465717"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458088,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140458088,"clinical_significance":[],"seq_region_name":"7","id":"rs1794516308"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458089,"source":"dbSNP","strand":1,"feature_type":"variation","end":140458089,"alleles":["T","A"],"id":"rs991583763","seq_region_name":"7","clinical_significance":[]},{"end":140458090,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140458090,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794516432","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140458094,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458094,"source":"dbSNP","seq_region_name":"7","id":"rs1794516487","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140458095,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458095,"source":"dbSNP","seq_region_name":"7","id":"rs1409346957","clinical_significance":[]},{"alleles":["A","G"],"end":140458096,"feature_type":"variation","strand":1,"source":"dbSNP","start":140458096,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs916075252"},{"seq_region_name":"7","id":"rs942174117","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140458097,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458097,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140458098,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458098,"clinical_significance":[],"seq_region_name":"7","id":"rs963285967"},{"alleles":["G","A","T"],"end":140458099,"feature_type":"variation","strand":1,"source":"dbSNP","start":140458099,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1442859797"},{"clinical_significance":[],"id":"rs796202249","seq_region_name":"7","end":140458100,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140458100,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs974093152","seq_region_name":"7","source":"dbSNP","start":140458101,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140458101,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1204303447","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458102,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140458102},{"strand":1,"feature_type":"variation","end":140458103,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458103,"source":"dbSNP","seq_region_name":"7","id":"rs1452644188","clinical_significance":[]},{"start":140458108,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140458108,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794517171","clinical_significance":[]},{"start":140458110,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140458110,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs374034700","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1247447149","end":140458111,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140458111,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140458116,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458116,"source":"dbSNP","seq_region_name":"7","id":"rs368871788","clinical_significance":[]},{"id":"rs560370753","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140458121,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458121,"source":"dbSNP"},{"alleles":["A","G"],"end":140458123,"feature_type":"variation","strand":1,"source":"dbSNP","start":140458123,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794517467"},{"strand":1,"feature_type":"variation","end":140458126,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458126,"source":"dbSNP","id":"rs1794517516","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","A"],"end":140458127,"strand":1,"feature_type":"variation","start":140458127,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs890789518","clinical_significance":[]},{"start":140458130,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140458130,"alleles":["A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794517645","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794517713","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458134,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140458134},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458136,"source":"dbSNP","strand":1,"feature_type":"variation","end":140458136,"alleles":["A","C"],"seq_region_name":"7","id":"rs943793293","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794517773","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458137,"feature_type":"variation","strand":1,"end":140458137,"alleles":["G","C"]},{"feature_type":"variation","strand":1,"end":140458138,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458138,"clinical_significance":[],"seq_region_name":"7","id":"rs930064413"},{"clinical_significance":[],"seq_region_name":"7","id":"rs185298572","source":"dbSNP","start":140458142,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140458142,"alleles":["T","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1375219444","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458143,"source":"dbSNP","strand":1,"feature_type":"variation","end":140458143,"alleles":["A","G"]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140458144,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458144,"source":"dbSNP","id":"rs1047117802","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1277519618","source":"dbSNP","start":140458145,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C","T"],"end":140458145,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1451227865","clinical_significance":[],"alleles":["C","T"],"end":140458150,"strand":1,"feature_type":"variation","start":140458150,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140458152,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458152,"clinical_significance":[],"id":"rs1794518919","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1794518985","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458154,"source":"dbSNP","strand":1,"feature_type":"variation","end":140458154,"alleles":["C","CC"]},{"seq_region_name":"7","id":"rs1794519046","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458156,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140458156},{"start":140458168,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140458168,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794519101","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs151178789","source":"dbSNP","start":140458173,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140458173,"alleles":["C","T"],"feature_type":"variation","strand":1},{"start":140458174,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140458174,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794519242","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140458175,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458175,"clinical_significance":[],"seq_region_name":"7","id":"rs751013677"},{"seq_region_name":"7","id":"rs537084554","clinical_significance":[],"end":140458181,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","start":140458181,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794519474","source":"dbSNP","start":140458181,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["ATAT","AT"],"end":140458184,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458182,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","TT"],"end":140458182,"seq_region_name":"7","id":"rs1422803825","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458182,"source":"dbSNP","strand":1,"feature_type":"variation","end":140458182,"alleles":["T","A","C"],"seq_region_name":"7","id":"rs1461721539","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794519659","feature_type":"variation","strand":1,"end":140458184,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458184},{"strand":1,"feature_type":"variation","end":140458188,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458188,"source":"dbSNP","seq_region_name":"7","id":"rs1039841235","clinical_significance":[]},{"start":140458189,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140458189,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1159442022","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458192,"source":"dbSNP","strand":1,"feature_type":"variation","end":140458192,"alleles":["G","A"],"seq_region_name":"7","id":"rs1794519826","clinical_significance":[]},{"end":140458194,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140458194,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794519887","clinical_significance":[]},{"id":"rs1441732798","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140458199,"strand":1,"feature_type":"variation","start":140458199,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1406089366","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458201,"source":"dbSNP","strand":1,"feature_type":"variation","end":140458201,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs900134337","alleles":["T","C"],"end":140458202,"feature_type":"variation","strand":1,"source":"dbSNP","start":140458202,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1478564631","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140458204,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458204},{"seq_region_name":"7","id":"rs1404451162","clinical_significance":[],"strand":1,"feature_type":"variation","end":140458206,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458206,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140458211,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458211,"clinical_significance":[],"id":"rs1585465971","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1794520293","clinical_significance":[],"strand":1,"feature_type":"variation","end":140458213,"alleles":["TT","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458212,"source":"dbSNP"},{"end":140458216,"alleles":["T","TT"],"strand":1,"feature_type":"variation","start":140458216,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130255702","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458218,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140458218,"id":"rs1220978755","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458219,"source":"dbSNP","strand":1,"feature_type":"variation","end":140458219,"alleles":["C","T"],"seq_region_name":"7","id":"rs1794520403","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794520447","feature_type":"variation","strand":1,"end":140458222,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458222},{"end":140458223,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140458223,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1001055790"},{"strand":1,"feature_type":"variation","end":140458227,"alleles":["T","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458227,"source":"dbSNP","seq_region_name":"7","id":"rs1489627522","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458228,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140458228,"seq_region_name":"7","id":"rs1794520648","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458230,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140458230,"clinical_significance":[],"seq_region_name":"7","id":"rs1794520739"},{"alleles":["T","C"],"end":140458231,"feature_type":"variation","strand":1,"source":"dbSNP","start":140458231,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1053416684"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140458233,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458233,"clinical_significance":[],"id":"rs1794520922","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140458234,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458234,"clinical_significance":[],"seq_region_name":"7","id":"rs531598102"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1216749050","source":"dbSNP","start":140458239,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140458239,"alleles":["A","C"],"feature_type":"variation","strand":1},{"alleles":["A","G"],"end":140458243,"feature_type":"variation","strand":1,"source":"dbSNP","start":140458243,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794521219"},{"id":"rs1314999306","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140458244,"strand":1,"feature_type":"variation","start":140458244,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1318302102","seq_region_name":"7","clinical_significance":[],"end":140458245,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","start":140458245,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1304416598","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140458246,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458246},{"seq_region_name":"7","id":"rs1585466038","clinical_significance":[],"end":140458250,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140458250,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458252,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["-","AG"],"end":140458251,"seq_region_name":"7","id":"rs1222987699","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140458255,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458255,"source":"dbSNP","seq_region_name":"7","id":"rs1011379653","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794521947","end":140458258,"alleles":["AA","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140458257,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140458260,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140458260,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794522043","clinical_significance":[]},{"end":140458261,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140458261,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs190113835","seq_region_name":"7","clinical_significance":[]},{"start":140458266,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140458266,"strand":1,"feature_type":"variation","id":"rs1009731489","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794522317","feature_type":"variation","strand":1,"alleles":["AA","AAA"],"end":140458269,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458268},{"seq_region_name":"7","id":"rs1794522411","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["ACT","-"],"end":140458271,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458269,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1794522502","seq_region_name":"7","alleles":["T","C"],"end":140458274,"feature_type":"variation","strand":1,"source":"dbSNP","start":140458274,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794522598","source":"dbSNP","start":140458278,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140458278,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1024690517","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140458279,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458279,"source":"dbSNP"},{"alleles":["A","G"],"end":140458281,"strand":1,"feature_type":"variation","start":140458281,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794522768","clinical_significance":[]},{"id":"rs1231218996","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458281,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AAAAA","AAAAAA"],"end":140458285},{"alleles":["A","G"],"end":140458284,"strand":1,"feature_type":"variation","start":140458284,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585466090","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458285,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140458285,"clinical_significance":[],"seq_region_name":"7","id":"rs1794523044"},{"start":140458294,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140458294,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs970874699","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs747399670","end":140458295,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140458295,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1002080804","source":"dbSNP","start":140458297,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A","C"],"end":140458297,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140458299,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140458303,"alleles":["GCCAT","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1298834684"},{"end":140458301,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140458301,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1307272064","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1210391034","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458305,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140458305},{"start":140458309,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140458309,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs757765047","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794523877","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458311,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140458311},{"seq_region_name":"7","id":"rs1158740842","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458313,"source":"dbSNP","strand":1,"feature_type":"variation","end":140458313,"alleles":["A","G"]},{"clinical_significance":[],"id":"rs1794524056","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458314,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140458314},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458317,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140458317,"id":"rs1794524161","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794524263","end":140458330,"alleles":["AAAA","AAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140458327,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140458329,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140458329,"alleles":["A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585466137","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458330,"source":"dbSNP","strand":1,"feature_type":"variation","end":140458330,"alleles":["A","G"],"seq_region_name":"7","id":"rs1794524457","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794524553","feature_type":"variation","strand":1,"end":140458335,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458335},{"strand":1,"feature_type":"variation","end":140458336,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458336,"source":"dbSNP","id":"rs1794524645","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1415392156","seq_region_name":"7","end":140458347,"alleles":["ACGGCTACACG","ACG"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140458337,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1459608309","clinical_significance":[],"start":140458338,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140458338,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs73485151","clinical_significance":[],"start":140458339,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140458339,"strand":1,"feature_type":"variation"},{"id":"rs1197858963","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458342,"source":"dbSNP","strand":1,"feature_type":"variation","end":140458342,"alleles":["T","G"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458344,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140458344,"clinical_significance":[],"seq_region_name":"7","id":"rs1794525160"},{"id":"rs781651425","seq_region_name":"7","clinical_significance":[],"start":140458346,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140458346,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs140214755","source":"dbSNP","start":140458347,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140458347,"alleles":["G","A"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140458349,"alleles":["-","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458350,"source":"dbSNP","seq_region_name":"7","id":"rs1794525360","clinical_significance":[]},{"end":140458350,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140458350,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1193667281","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458356,"source":"dbSNP","strand":1,"feature_type":"variation","end":140458356,"alleles":["C","T"],"seq_region_name":"7","id":"rs1186577109","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794525620","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458360,"source":"dbSNP","strand":1,"feature_type":"variation","end":140458360,"alleles":["G","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458363,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140458363,"seq_region_name":"7","id":"rs1794525710","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794525805","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140458365,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458365,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794525895","source":"dbSNP","start":140458371,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140458371,"alleles":["A","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1794525988","clinical_significance":[],"end":140458377,"alleles":["TAT","T"],"strand":1,"feature_type":"variation","start":140458375,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458376,"source":"dbSNP","strand":1,"feature_type":"variation","end":140458376,"alleles":["A","G"],"seq_region_name":"7","id":"rs991987035","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458377,"source":"dbSNP","strand":1,"feature_type":"variation","end":140458377,"alleles":["T","C"],"id":"rs1258565983","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794526288","alleles":["T","C"],"end":140458384,"feature_type":"variation","strand":1,"source":"dbSNP","start":140458384,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140458389,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140458389,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794526385"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458392,"source":"dbSNP","strand":1,"feature_type":"variation","end":140458392,"alleles":["G","A","C"],"seq_region_name":"7","id":"rs1794526480","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794526588","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140458393,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458393,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458395,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140458395,"clinical_significance":[],"seq_region_name":"7","id":"rs951374971"},{"source":"dbSNP","start":140458400,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140458400,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs745418376"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140458401,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458401,"source":"dbSNP","seq_region_name":"7","id":"rs1023027971","clinical_significance":[]},{"seq_region_name":"7","id":"rs780628593","clinical_significance":[],"alleles":["G","C","T"],"end":140458410,"strand":1,"feature_type":"variation","start":140458410,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1794527125","seq_region_name":"7","alleles":["C","T"],"end":140458413,"feature_type":"variation","strand":1,"source":"dbSNP","start":140458413,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794527221","end":140458414,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140458414,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458416,"feature_type":"variation","strand":1,"end":140458416,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794527294"},{"feature_type":"variation","strand":1,"end":140458418,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458418,"clinical_significance":[],"seq_region_name":"7","id":"rs1379542779"},{"end":140458420,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140458420,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794527479","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs912683476","source":"dbSNP","start":140458422,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140458422,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140458423,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140458423,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs973626703","seq_region_name":"7"},{"start":140458426,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140458426,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794527800","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140458434,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458434,"source":"dbSNP","id":"rs182872507","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794528016","alleles":["G","A"],"end":140458437,"feature_type":"variation","strand":1,"source":"dbSNP","start":140458437,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140458439,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458439,"source":"dbSNP","seq_region_name":"7","id":"rs1336208035","clinical_significance":[]},{"id":"rs1389465078","seq_region_name":"7","clinical_significance":[],"start":140458444,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140458444,"alleles":["C","A","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1360029165","feature_type":"variation","strand":1,"end":140458447,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458447},{"seq_region_name":"7","id":"rs1794528447","clinical_significance":[],"alleles":["A","G"],"end":140458448,"strand":1,"feature_type":"variation","start":140458448,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140458450,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458450,"clinical_significance":[],"seq_region_name":"7","id":"rs1288488948"},{"alleles":["AGGCCAATCCAGAGACAAAGCAG","AGGCCAATCCAGAGACAAAGCAGGCCAATCCAGAGACAAAGCAG"],"end":140458473,"feature_type":"variation","strand":1,"source":"dbSNP","start":140458451,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130256840"},{"feature_type":"variation","strand":1,"end":140458453,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458453,"clinical_significance":[],"id":"rs975577724","seq_region_name":"7"},{"alleles":["A","G"],"end":140458456,"feature_type":"variation","strand":1,"source":"dbSNP","start":140458456,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs150342793"},{"clinical_significance":[],"id":"rs1794528848","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140458460,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458460},{"start":140458466,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140458466,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs921421128","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458467,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140458467,"clinical_significance":[],"seq_region_name":"7","id":"rs987648092"},{"feature_type":"variation","strand":1,"end":140458470,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458470,"clinical_significance":[],"seq_region_name":"7","id":"rs1174672571"},{"feature_type":"variation","strand":1,"end":140458473,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458473,"clinical_significance":[],"seq_region_name":"7","id":"rs1469626589"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1287562836","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458477,"feature_type":"variation","strand":1,"end":140458477,"alleles":["C","G","T"]},{"seq_region_name":"7","id":"rs912230500","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458478,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140458478},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458482,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140458482,"clinical_significance":[],"seq_region_name":"7","id":"rs1361735450"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794529708","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140458483,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458483},{"clinical_significance":[],"seq_region_name":"7","id":"rs936940880","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458487,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140458487},{"feature_type":"variation","strand":1,"end":140458489,"alleles":["G","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458489,"clinical_significance":[],"seq_region_name":"7","id":"rs1053941924"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458491,"source":"dbSNP","strand":1,"feature_type":"variation","end":140458491,"alleles":["G","C"],"seq_region_name":"7","id":"rs1794529980","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs78467230","feature_type":"variation","strand":1,"end":140458495,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458495},{"id":"rs768778027","seq_region_name":"7","clinical_significance":[],"start":140458497,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140458497,"alleles":["G","A","T"],"strand":1,"feature_type":"variation"},{"id":"rs781287692","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140458501,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458501,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1244608696","source":"dbSNP","start":140458501,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140458502,"alleles":["GG","G"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140458502,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458502,"clinical_significance":[],"seq_region_name":"7","id":"rs1046482737"},{"start":140458503,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140458503,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794530633","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140458506,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458506,"clinical_significance":[],"seq_region_name":"7","id":"rs1794530726"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1201468819","feature_type":"variation","strand":1,"end":140458512,"alleles":["AAA","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458510},{"clinical_significance":[],"id":"rs1460758780","seq_region_name":"7","feature_type":"variation","strand":1,"end":140458513,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458513},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458515,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140458515,"seq_region_name":"7","id":"rs1794530988","clinical_significance":[]},{"seq_region_name":"7","id":"rs906304739","clinical_significance":[],"strand":1,"feature_type":"variation","end":140458516,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458516,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130257169","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140458528,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458528},{"seq_region_name":"7","id":"rs1303831968","clinical_significance":[],"strand":1,"feature_type":"variation","end":140458532,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458532,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1229589058","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458534,"feature_type":"variation","strand":1,"end":140458534,"alleles":["G","A"]},{"end":140458537,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140458537,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1305809730"},{"start":140458540,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140458540,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs367939250","clinical_significance":[]},{"seq_region_name":"7","id":"rs1222512473","clinical_significance":[],"start":140458544,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140458544,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1794531696","seq_region_name":"7","end":140458545,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140458545,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458551,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140458551,"seq_region_name":"7","id":"rs1228989687","clinical_significance":[]},{"alleles":["A","G"],"end":140458563,"strand":1,"feature_type":"variation","start":140458563,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1001939359","clinical_significance":[]},{"id":"rs1039872538","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140458567,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458567,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1033524694","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458572,"feature_type":"variation","strand":1,"end":140458572,"alleles":["G","T"]},{"alleles":["G","A"],"end":140458573,"feature_type":"variation","strand":1,"source":"dbSNP","start":140458573,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1452351561","seq_region_name":"7"},{"end":140458574,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140458574,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794531993"},{"seq_region_name":"7","id":"rs1794532052","clinical_significance":[],"end":140458577,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140458577,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140458580,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140458580,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794532121","clinical_significance":[]},{"end":140458582,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140458582,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs570385319","seq_region_name":"7"},{"seq_region_name":"7","id":"rs994758829","clinical_significance":[],"strand":1,"feature_type":"variation","end":140458584,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458584,"source":"dbSNP"},{"alleles":["T","C"],"end":140458585,"feature_type":"variation","strand":1,"source":"dbSNP","start":140458585,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1042948170","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140458586,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458586,"source":"dbSNP","seq_region_name":"7","id":"rs1794532385","clinical_significance":[]},{"seq_region_name":"7","id":"rs903008775","clinical_significance":[],"strand":1,"feature_type":"variation","end":140458593,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458593,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs537853675","feature_type":"variation","strand":1,"end":140458597,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458597},{"strand":1,"feature_type":"variation","end":140458601,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458601,"source":"dbSNP","seq_region_name":"7","id":"rs1794532569","clinical_significance":[]},{"source":"dbSNP","start":140458602,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140458602,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1169064189","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458604,"source":"dbSNP","strand":1,"feature_type":"variation","end":140458604,"alleles":["A","G"],"id":"rs1026198039","seq_region_name":"7","clinical_significance":[]},{"end":140458606,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140458606,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794532759"},{"source":"dbSNP","start":140458609,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140458609,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794532832"},{"end":140458616,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140458616,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794532888","clinical_significance":[]},{"seq_region_name":"7","id":"rs1444720319","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140458621,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458621,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1386704860","seq_region_name":"7","feature_type":"variation","strand":1,"end":140458655,"alleles":["AAGATTAAACATATTCAATGTGAATCTCAGAA","AA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458624},{"alleles":["A","G"],"end":140458627,"feature_type":"variation","strand":1,"source":"dbSNP","start":140458627,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs138027938"},{"id":"rs1794533176","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140458630,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458630,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1460689866","clinical_significance":[],"alleles":["C","T"],"end":140458633,"strand":1,"feature_type":"variation","start":140458633,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140458638,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140458638,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1794533317","seq_region_name":"7","clinical_significance":[]},{"id":"rs982843407","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140458639,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458639,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1197373803","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140458640,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458640},{"id":"rs1794533484","seq_region_name":"7","clinical_significance":[],"end":140458641,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140458641,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1794533549","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458642,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140458642},{"clinical_significance":[],"seq_region_name":"7","id":"rs574810275","end":140458643,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140458643,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794533671","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140458644,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458644},{"start":140458646,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140458646,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1012893059","clinical_significance":[]},{"end":140458653,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140458653,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1222316183","clinical_significance":[]},{"source":"dbSNP","start":140458658,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["ATTATT","ATT"],"end":140458663,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1023374540"},{"seq_region_name":"7","id":"rs1794533926","clinical_significance":[],"start":140458661,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140458661,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458662,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140458662,"clinical_significance":[],"seq_region_name":"7","id":"rs75040063"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563087567","feature_type":"variation","strand":1,"end":140458667,"alleles":["TTTTTT","TTTTT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458662},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458664,"feature_type":"variation","strand":1,"end":140458664,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs963518267"},{"seq_region_name":"7","id":"rs187511699","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140458665,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458665,"source":"dbSNP"},{"alleles":["T","C"],"end":140458667,"feature_type":"variation","strand":1,"source":"dbSNP","start":140458667,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585466554"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458676,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AAAAAAA","AAAAAA"],"end":140458682,"seq_region_name":"7","id":"rs1026475522","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130257795","clinical_significance":[],"strand":1,"feature_type":"variation","end":140458681,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458681,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140458683,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458683,"source":"dbSNP","seq_region_name":"7","id":"rs1794534407","clinical_significance":[]},{"seq_region_name":"7","id":"rs1309539755","clinical_significance":[],"strand":1,"feature_type":"variation","end":140458687,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458687,"source":"dbSNP"},{"seq_region_name":"7","id":"rs2130257854","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140458688,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458688,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs558102149","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458696,"feature_type":"variation","strand":1,"end":140458696,"alleles":["T","C","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130257882","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458697,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140458697},{"clinical_significance":[],"seq_region_name":"7","id":"rs141075134","alleles":["C","G"],"end":140458700,"feature_type":"variation","strand":1,"source":"dbSNP","start":140458700,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140458701,"alleles":["T","TT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140458701,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1396322872"},{"strand":1,"feature_type":"variation","end":140458701,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458701,"source":"dbSNP","seq_region_name":"7","id":"rs1458850327","clinical_significance":[]},{"id":"rs1157581875","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140458709,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458709,"source":"dbSNP"},{"end":140458710,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140458710,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1345169636"},{"start":140458715,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140458715,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1437769062","clinical_significance":[]},{"start":140458717,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140458717,"alleles":["G","C"],"strand":1,"feature_type":"variation","id":"rs1443593075","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1295720686","seq_region_name":"7","alleles":["CTTCTT","CTT"],"end":140458725,"feature_type":"variation","strand":1,"source":"dbSNP","start":140458720,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1344007489","alleles":["T","C"],"end":140458722,"feature_type":"variation","strand":1,"source":"dbSNP","start":140458722,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140458724,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458724,"clinical_significance":[],"seq_region_name":"7","id":"rs912117312"},{"end":140458730,"alleles":["TTTTTTT","TTTT","TTTTTT","TTTTTTTT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140458724,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1563087605"},{"strand":1,"feature_type":"variation","end":140458727,"alleles":["T","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458727,"source":"dbSNP","id":"rs1417090470","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1249711202","clinical_significance":[],"start":140458728,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140458728,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140458730,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140458730,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs921453625"},{"seq_region_name":"7","id":"rs1403965343","clinical_significance":[],"end":140458731,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140458731,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1794536030","seq_region_name":"7","source":"dbSNP","start":140458731,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140458731,"alleles":["C","CC"],"feature_type":"variation","strand":1},{"id":"rs1794536087","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140458734,"strand":1,"feature_type":"variation","start":140458734,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458736,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140458736,"id":"rs1288518021","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1330648309","alleles":["C","T"],"end":140458737,"feature_type":"variation","strand":1,"source":"dbSNP","start":140458737,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1221529691","feature_type":"variation","strand":1,"end":140458738,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458738},{"strand":1,"feature_type":"variation","end":140458739,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458739,"source":"dbSNP","seq_region_name":"7","id":"rs1282919124","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458743,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140458743,"clinical_significance":[],"seq_region_name":"7","id":"rs1794536439"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794536489","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458744,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140458744},{"seq_region_name":"7","id":"rs1794536574","clinical_significance":[],"end":140458747,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140458747,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1794536635","clinical_significance":[],"start":140458749,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140458749,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1289629608","feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140458758,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458758},{"feature_type":"variation","strand":1,"alleles":["CGATC","CGATCGATC"],"end":140458762,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458758,"clinical_significance":[],"seq_region_name":"7","id":"rs1490851352"},{"id":"rs1351600047","seq_region_name":"7","clinical_significance":[],"end":140458759,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140458759,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["T","C"],"end":140458761,"strand":1,"feature_type":"variation","start":140458761,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1322300060","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140458763,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458763,"clinical_significance":[],"seq_region_name":"7","id":"rs2130258274"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1223669621","source":"dbSNP","start":140458764,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140458764,"feature_type":"variation","strand":1},{"end":140458765,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140458765,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs936805574","clinical_significance":[]},{"start":140458767,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140458767,"strand":1,"feature_type":"variation","id":"rs989597545","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs774251565","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458772,"feature_type":"variation","strand":1,"end":140458772,"alleles":["C","T"]},{"alleles":["C","G"],"end":140458776,"strand":1,"feature_type":"variation","start":140458776,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794537247","clinical_significance":[]},{"seq_region_name":"7","id":"rs1407344651","clinical_significance":[],"start":140458781,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140458781,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140458783,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140458783,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1344206216"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458784,"source":"dbSNP","strand":1,"feature_type":"variation","end":140458784,"alleles":["T","C"],"seq_region_name":"7","id":"rs1794537441","clinical_significance":[]},{"seq_region_name":"7","id":"rs914197218","clinical_significance":[],"start":140458787,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140458787,"alleles":["C","G","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1794537576","clinical_significance":[],"alleles":["G","C"],"end":140458791,"strand":1,"feature_type":"variation","start":140458791,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1423472082","clinical_significance":[],"start":140458792,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140458792,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140458795,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458795,"source":"dbSNP","seq_region_name":"7","id":"rs1794537694","clinical_significance":[]},{"clinical_significance":[],"id":"rs7784558","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140458796,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458796},{"seq_region_name":"7","id":"rs1794537900","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458804,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["-","C"],"end":140458803},{"source":"dbSNP","start":140458804,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140458804,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1042791482"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794538014","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458805,"feature_type":"variation","strand":1,"alleles":["GCCTCCATGCCCAG","G"],"end":140458818},{"clinical_significance":[],"seq_region_name":"7","id":"rs1678693660","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140458807,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458807},{"start":140458810,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140458810,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130258501","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1160011826","source":"dbSNP","start":140458818,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140458818,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140458819,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TT","T"],"end":140458820,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1451325331"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140458824,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458824,"clinical_significance":[],"seq_region_name":"7","id":"rs1363048274"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458831,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140458831,"clinical_significance":[],"id":"rs546240478","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458837,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140458837,"id":"rs1199006712","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1046092098","source":"dbSNP","start":140458838,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140458838,"feature_type":"variation","strand":1},{"end":140458841,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140458841,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs906162670","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130258606","clinical_significance":[],"start":140458844,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140458844,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1198698984","clinical_significance":[],"end":140458846,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140458846,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1175595966","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140458848,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458848},{"clinical_significance":[],"seq_region_name":"7","id":"rs1264106478","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140458849,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458849},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458850,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140458850,"seq_region_name":"7","id":"rs937762488","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130258677","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458856,"feature_type":"variation","strand":1,"end":140458856,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1057086049","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140458859,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458859,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140458860,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458860,"source":"dbSNP","seq_region_name":"7","id":"rs1794538980","clinical_significance":[]},{"start":140458867,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140458867,"alleles":["G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1350372295","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458868,"source":"dbSNP","strand":1,"feature_type":"variation","end":140458868,"alleles":["C","T"],"seq_region_name":"7","id":"rs564439528","clinical_significance":[]},{"alleles":["C","T"],"end":140458869,"feature_type":"variation","strand":1,"source":"dbSNP","start":140458869,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1225762374"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458874,"source":"dbSNP","strand":1,"feature_type":"variation","end":140458874,"alleles":["A","G"],"id":"rs895762796","seq_region_name":"7","clinical_significance":[]},{"end":140458875,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140458875,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1283213752"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1013231987","source":"dbSNP","start":140458877,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140458877,"alleles":["G","A"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140458878,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458878,"source":"dbSNP","seq_region_name":"7","id":"rs1326550558","clinical_significance":[]},{"end":140458883,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140458883,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794539480","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140458884,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458884,"clinical_significance":[],"seq_region_name":"7","id":"rs1794539534"},{"seq_region_name":"7","id":"rs368309724","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140458888,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458888,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458890,"feature_type":"variation","strand":1,"alleles":["A","AA"],"end":140458890,"clinical_significance":[],"seq_region_name":"7","id":"rs760681788"},{"seq_region_name":"7","id":"rs899153968","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458894,"source":"dbSNP","strand":1,"feature_type":"variation","end":140458894,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs1794539779","clinical_significance":[],"alleles":["C","A"],"end":140458895,"strand":1,"feature_type":"variation","start":140458895,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs899006355","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458899,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140458899},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585466924","alleles":["A","G"],"end":140458901,"feature_type":"variation","strand":1,"source":"dbSNP","start":140458901,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140458903,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458903,"clinical_significance":[],"seq_region_name":"7","id":"rs1383815157"},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140458904,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458904,"clinical_significance":[],"seq_region_name":"7","id":"rs1794539988"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1176812809","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458905,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140458905},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458909,"source":"dbSNP","strand":1,"feature_type":"variation","end":140458909,"alleles":["A","G","T"],"id":"rs994883624","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794540207","clinical_significance":[],"end":140458910,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140458910,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140458911,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140458911,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1211016251","seq_region_name":"7"},{"end":140458912,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140458912,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1364104410"},{"source":"dbSNP","start":140458913,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140458913,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794540371"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1424382367","alleles":["C","T"],"end":140458915,"feature_type":"variation","strand":1,"source":"dbSNP","start":140458915,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1175690169","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458917,"feature_type":"variation","strand":1,"end":140458917,"alleles":["A","C","G","T"]},{"end":140458920,"alleles":["G","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140458920,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1475770352"},{"end":140458923,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140458923,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1374903846","seq_region_name":"7","clinical_significance":[]},{"end":140458927,"alleles":["TCTCT","TCTCTCT"],"strand":1,"feature_type":"variation","start":140458923,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794540670","clinical_significance":[]},{"source":"dbSNP","start":140458924,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140458924,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794540748"},{"seq_region_name":"7","id":"rs1026332627","clinical_significance":[],"end":140458928,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140458928,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1794540874","seq_region_name":"7","clinical_significance":[],"end":140458929,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140458929,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["A","G"],"end":140458933,"strand":1,"feature_type":"variation","start":140458933,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1446592793","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140458936,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458936,"clinical_significance":[],"seq_region_name":"7","id":"rs1794540993"},{"source":"dbSNP","start":140458940,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140458940,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs994707901"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794541128","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458942,"feature_type":"variation","strand":1,"end":140458942,"alleles":["A","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458944,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140458944,"seq_region_name":"7","id":"rs1205901171","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794541248","source":"dbSNP","start":140458947,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140458947,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs950898780","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458949,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140458949},{"alleles":["G","-"],"end":140458949,"feature_type":"variation","strand":1,"source":"dbSNP","start":140458949,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794541388"},{"end":140458953,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140458953,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1009048844","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794541433","feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140458954,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458954},{"start":140458956,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140458956,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1026565101","clinical_significance":[]},{"alleles":["T","G"],"end":140458963,"feature_type":"variation","strand":1,"source":"dbSNP","start":140458963,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs762096174","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1342121217","seq_region_name":"7","source":"dbSNP","start":140458965,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140458965,"alleles":["A","T"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140458967,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458967,"source":"dbSNP","seq_region_name":"7","id":"rs1262281840","clinical_significance":[]},{"clinical_significance":[],"id":"rs1794541747","seq_region_name":"7","alleles":["A","T"],"end":140458971,"feature_type":"variation","strand":1,"source":"dbSNP","start":140458971,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs767882014","clinical_significance":[],"start":140458972,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140458972,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140458973,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458973,"clinical_significance":[],"seq_region_name":"7","id":"rs750465224"},{"seq_region_name":"7","id":"rs1794541936","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458976,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140458976},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458978,"source":"dbSNP","strand":1,"feature_type":"variation","end":140458978,"alleles":["A","G"],"seq_region_name":"7","id":"rs1350001782","clinical_significance":[]},{"clinical_significance":[],"id":"rs1271378354","seq_region_name":"7","alleles":["T","C"],"end":140458979,"feature_type":"variation","strand":1,"source":"dbSNP","start":140458979,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1269670285","seq_region_name":"7","clinical_significance":[],"start":140458981,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["ACACACACA","ACACACA"],"end":140458989,"strand":1,"feature_type":"variation"},{"alleles":["C","G","T"],"end":140458986,"feature_type":"variation","strand":1,"source":"dbSNP","start":140458986,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1563087734","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1197534589","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140458988,"source":"dbSNP","strand":1,"feature_type":"variation","end":140458988,"alleles":["C","A","T"]},{"end":140458995,"alleles":["CATCTCCC","CATCTCCCATCTCCC"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140458988,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs759705592"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458991,"feature_type":"variation","strand":1,"end":140458991,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs75395312"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140458993,"feature_type":"variation","strand":1,"end":140458995,"alleles":["CCC","CCCCC"],"clinical_significance":[],"id":"rs768670161","seq_region_name":"7"},{"start":140458997,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G","T"],"end":140458997,"strand":1,"feature_type":"variation","id":"rs765153094","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs752569362","end":140459000,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140459000,"consequence_type":"splice_region_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs758391912","seq_region_name":"7","source":"dbSNP","start":140459008,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140459008,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794542814","feature_type":"variation","strand":1,"end":140459013,"alleles":["A","G"],"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459013},{"seq_region_name":"7","id":"rs1794542910","clinical_significance":[],"alleles":["C","T"],"end":140459016,"strand":1,"feature_type":"variation","start":140459016,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1164824411","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459017,"feature_type":"variation","strand":1,"end":140459017,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1365641693","end":140459018,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140459018,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs368732188","clinical_significance":[],"strand":1,"feature_type":"variation","end":140459019,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140459019,"source":"dbSNP"},{"clinical_significance":["uncertain significance"],"seq_region_name":"7","id":"rs751399882","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459020,"feature_type":"variation","strand":1,"end":140459020,"alleles":["G","A"]},{"alleles":["G","T"],"end":140459028,"feature_type":"variation","strand":1,"source":"dbSNP","start":140459028,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1366393908"},{"alleles":["C","T"],"end":140459030,"feature_type":"variation","strand":1,"source":"dbSNP","start":140459030,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1391635687"},{"source":"dbSNP","start":140459037,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140459037,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs543440285"},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459038,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140459038,"clinical_significance":[],"seq_region_name":"7","id":"rs780731227"},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140459039,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140459039,"seq_region_name":"7","id":"rs745327289","clinical_significance":["likely benign"]},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140459042,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140459042,"source":"dbSNP","seq_region_name":"7","id":"rs769194879","clinical_significance":[]},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459045,"feature_type":"variation","strand":1,"end":140459045,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794543923"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794544008","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140459048,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459048},{"source":"dbSNP","start":140459051,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140459051,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2272095"},{"seq_region_name":"7","id":"rs1220278760","clinical_significance":[],"start":140459052,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140459052,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"id":"rs749788549","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140459059,"source":"dbSNP","strand":1,"feature_type":"variation","end":140459059,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1179208302","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140459065,"source":"dbSNP","strand":1,"feature_type":"variation","end":140459065,"alleles":["A","G"]},{"assembly_name":"GRCh38","consequence_type":"frameshift_variant","start":140459065,"source":"dbSNP","strand":1,"feature_type":"variation","end":140459066,"alleles":["AT","-"],"id":"rs1481061193","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140459066,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459066,"clinical_significance":[],"seq_region_name":"7","id":"rs769326339"},{"clinical_significance":[],"seq_region_name":"7","id":"rs774816515","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459069,"feature_type":"variation","strand":1,"end":140459069,"alleles":["C","G"]},{"id":"rs1184750363","seq_region_name":"7","clinical_significance":[],"end":140459070,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140459070,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1185726452","alleles":["A","G"],"end":140459073,"feature_type":"variation","strand":1,"source":"dbSNP","start":140459073,"consequence_type":"synonymous_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1387560171","clinical_significance":[],"strand":1,"feature_type":"variation","end":140459075,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140459075,"source":"dbSNP"},{"seq_region_name":"7","id":"rs762286472","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140459078,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140459078,"source":"dbSNP"},{"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459079,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140459079,"clinical_significance":[],"id":"rs1794545131","seq_region_name":"7"},{"seq_region_name":"7","id":"rs775269221","clinical_significance":[],"end":140459082,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140459082,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"seq_region_name":"7","id":"rs200628844","clinical_significance":[],"alleles":["G","C","T"],"end":140459087,"strand":1,"feature_type":"variation","start":140459087,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"seq_region_name":"7","id":"rs1794545489","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140459089,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140459089,"source":"dbSNP"},{"seq_region_name":"7","id":"rs761022118","clinical_significance":[],"start":140459091,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","alleles":["C","T"],"end":140459091,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1299586064","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459092,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140459092},{"source":"dbSNP","start":140459093,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140459093,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs766358139"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1445679257","consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459094,"feature_type":"variation","strand":1,"end":140459094,"alleles":["A","G"]},{"feature_type":"variation","strand":1,"end":140459102,"alleles":["C","T"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459102,"clinical_significance":[],"seq_region_name":"7","id":"rs1794545917"},{"source":"dbSNP","start":140459103,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140459103,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs193237554","seq_region_name":"7"},{"end":140459105,"alleles":["C","A","G","T"],"strand":1,"feature_type":"variation","start":140459105,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs762850310","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1062761","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140459106,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459106},{"alleles":["T","A"],"end":140459109,"feature_type":"variation","strand":1,"source":"dbSNP","start":140459109,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1193564326"},{"id":"rs1794546425","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140459110,"strand":1,"feature_type":"variation","start":140459110,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140459117,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140459117,"source":"dbSNP","id":"rs1062760","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140459123,"source":"dbSNP","strand":1,"feature_type":"variation","end":140459123,"alleles":["C","A"],"id":"rs371500101","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459125,"feature_type":"variation","strand":1,"end":140459125,"alleles":["G","A"],"clinical_significance":[],"id":"rs757058688","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1455087216","end":140459126,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140459126,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140459127,"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140459127,"source":"dbSNP","seq_region_name":"7","id":"rs1315282299","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794546806","feature_type":"variation","strand":1,"end":140459131,"alleles":["T","C"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459131},{"seq_region_name":"7","id":"rs1206878475","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140459134,"source":"dbSNP","strand":1,"feature_type":"variation","end":140459134,"alleles":["G","C"]},{"clinical_significance":[],"id":"rs1249904011","seq_region_name":"7","source":"dbSNP","start":140459136,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140459136,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130260535","end":140459137,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140459137,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140459145,"alleles":["C","A"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459145,"clinical_significance":[],"id":"rs1173496457","seq_region_name":"7"},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459147,"feature_type":"variation","strand":1,"end":140459147,"alleles":["T","C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs767131876"},{"seq_region_name":"7","id":"rs1204647932","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140459148,"source":"dbSNP","strand":1,"feature_type":"variation","end":140459148,"alleles":["C","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794547320","feature_type":"variation","strand":1,"alleles":["TTT","TT"],"end":140459151,"consequence_type":"frameshift_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459149},{"seq_region_name":"7","id":"rs968752824","clinical_significance":[],"end":140459150,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140459150,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"seq_region_name":"7","id":"rs1245381626","clinical_significance":[],"alleles":["T","C"],"end":140459151,"strand":1,"feature_type":"variation","start":140459151,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant"},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459153,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140459153,"clinical_significance":[],"id":"rs750041308","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1062759","clinical_significance":[],"end":140459154,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140459154,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant"},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140459155,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140459155,"source":"dbSNP","seq_region_name":"7","id":"rs1794547728","clinical_significance":[]},{"seq_region_name":"7","id":"rs978527559","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140459157,"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140459157,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140459159,"alleles":["C","A","T"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459159,"clinical_significance":[],"id":"rs58548717","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs61736379","end":140459160,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140459160,"consequence_type":"synonymous_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs2130260838","seq_region_name":"7","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459161,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140459161},{"seq_region_name":"7","id":"rs183741395","clinical_significance":["uncertain significance"],"start":140459162,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140459162,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140459163,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","end":140459163,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs768286835"},{"clinical_significance":[],"id":"rs1420946013","seq_region_name":"7","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459164,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140459164},{"id":"rs1585467688","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140459165,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140459165},{"source":"dbSNP","start":140459166,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140459166,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs537817510"},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140459174,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140459174,"id":"rs1062758","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130260967","alleles":["T","C"],"end":140459189,"feature_type":"variation","strand":1,"source":"dbSNP","start":140459189,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"end":140459190,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140459190,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1464227654"},{"seq_region_name":"7","id":"rs1384858094","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C","T"],"end":140459191,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140459191,"source":"dbSNP"},{"clinical_significance":[],"id":"rs772316316","seq_region_name":"7","source":"dbSNP","start":140459192,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140459192,"feature_type":"variation","strand":1},{"end":140459193,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140459193,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","seq_region_name":"7","id":"rs1563087964","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794549145","clinical_significance":[],"start":140459195,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140459195,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140459196,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140459196,"source":"dbSNP","seq_region_name":"7","id":"rs1408073121","clinical_significance":[]},{"end":140459198,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140459198,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1231658205"},{"alleles":["G","A"],"end":140459199,"strand":1,"feature_type":"variation","start":140459199,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","seq_region_name":"7","id":"rs1450325559","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","A","G"],"end":140459200,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459200,"clinical_significance":["uncertain significance"],"seq_region_name":"7","id":"rs773681260"},{"clinical_significance":["uncertain significance"],"id":"rs747179489","seq_region_name":"7","alleles":["T","C"],"end":140459203,"feature_type":"variation","strand":1,"source":"dbSNP","start":140459203,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140459204,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140459204,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1216339444"},{"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459205,"feature_type":"variation","strand":1,"end":140459205,"alleles":["C","T"],"clinical_significance":[],"id":"rs1293544402","seq_region_name":"7"},{"end":140459218,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140459218,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs771227419","clinical_significance":[]},{"alleles":["T","C"],"end":140459219,"feature_type":"variation","strand":1,"source":"dbSNP","start":140459219,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1563087995","seq_region_name":"7"},{"alleles":["C","T"],"end":140459221,"feature_type":"variation","strand":1,"source":"dbSNP","start":140459221,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs776656605","seq_region_name":"7"},{"seq_region_name":"7","id":"rs2130261314","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140459223,"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140459223,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140459228,"source":"dbSNP","strand":1,"feature_type":"variation","end":140459228,"alleles":["G","A"],"seq_region_name":"7","id":"rs1372837990","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140459229,"source":"dbSNP","strand":1,"feature_type":"variation","end":140459229,"alleles":["C","G","T"],"seq_region_name":"7","id":"rs759635628","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140459230,"alleles":["G","A","C","T"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459230,"clinical_significance":[],"id":"rs763962930","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140459235,"consequence_type":"splice_acceptor_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459235,"clinical_significance":[],"id":"rs761808359","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs767193234","source":"dbSNP","start":140459237,"consequence_type":"splice_region_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140459237,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794550571","consequence_type":"splice_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459239,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140459239},{"source":"dbSNP","start":140459241,"consequence_type":"splice_region_variant","assembly_name":"GRCh38","end":140459241,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs750271181"},{"seq_region_name":"7","id":"rs1364927057","clinical_significance":[],"strand":1,"feature_type":"variation","end":140459244,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"splice_polypyrimidine_tract_variant","start":140459244,"source":"dbSNP"},{"id":"rs1224128315","seq_region_name":"7","clinical_significance":[],"end":140459245,"alleles":["T","TT"],"strand":1,"feature_type":"variation","start":140459245,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_polypyrimidine_tract_variant"},{"alleles":["A","C"],"end":140459249,"strand":1,"feature_type":"variation","start":140459249,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_polypyrimidine_tract_variant","seq_region_name":"7","id":"rs1794550831","clinical_significance":[]},{"end":140459250,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140459250,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_polypyrimidine_tract_variant","id":"rs376681323","seq_region_name":"7","clinical_significance":[]},{"start":140459254,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140459255,"alleles":["GG","G","GGG","GGGG"],"strand":1,"feature_type":"variation","id":"rs761670884","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140459256,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140459256,"source":"dbSNP","seq_region_name":"7","id":"rs374114177","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794551017","clinical_significance":[],"strand":1,"feature_type":"variation","end":140459259,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140459259,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140459260,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140459260,"source":"dbSNP","id":"rs766078366","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs966998078","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140459266,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140459266},{"seq_region_name":"7","id":"rs753336786","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140459268,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140459268},{"clinical_significance":[],"seq_region_name":"7","id":"rs1554447081","alleles":["G","C"],"end":140459270,"feature_type":"variation","strand":1,"source":"dbSNP","start":140459270,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140459279,"alleles":["ATAAGGCAT","AT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140459271,"source":"dbSNP","id":"rs767395132","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140459272,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140459272,"source":"dbSNP","seq_region_name":"7","id":"rs1794551376","clinical_significance":[]},{"start":140459273,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140459273,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs754536949","clinical_significance":[]},{"start":140459274,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C","T"],"end":140459274,"strand":1,"feature_type":"variation","id":"rs367973327","seq_region_name":"7","clinical_significance":[]},{"id":"rs763684136","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140459275,"source":"dbSNP","strand":1,"feature_type":"variation","end":140459275,"alleles":["G","C"]},{"feature_type":"variation","strand":1,"end":140459277,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459277,"clinical_significance":[],"id":"rs758996354","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1345658901","clinical_significance":[],"alleles":["G","A"],"end":140459280,"strand":1,"feature_type":"variation","start":140459280,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1432837397","seq_region_name":"7","feature_type":"variation","strand":1,"end":140459283,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459283},{"clinical_significance":[],"seq_region_name":"7","id":"rs1296376608","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459284,"feature_type":"variation","strand":1,"end":140459284,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs549833106","source":"dbSNP","start":140459285,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140459285,"alleles":["A","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794551871","end":140459286,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140459286,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140459288,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140459288,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794551922","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794551993","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["AGAGA","AGA"],"end":140459292,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140459288,"source":"dbSNP"},{"end":140459296,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140459296,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs927653771","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1158376081","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459300,"feature_type":"variation","strand":1,"end":140459300,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs1794552110","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140459303,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140459303},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459305,"feature_type":"variation","strand":1,"end":140459305,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1481026519"},{"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140459307,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459307,"clinical_significance":[],"seq_region_name":"7","id":"rs937626716"},{"seq_region_name":"7","id":"rs6966409","clinical_significance":[],"alleles":["G","A","C","T"],"end":140459308,"strand":1,"feature_type":"variation","start":140459308,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140459310,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AAAAAA","AAAAAAA"],"end":140459315,"seq_region_name":"7","id":"rs1794552407","clinical_significance":[]},{"seq_region_name":"7","id":"rs1272508204","clinical_significance":[],"strand":1,"feature_type":"variation","end":140459311,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140459311,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1794552538","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140459314,"source":"dbSNP","strand":1,"feature_type":"variation","end":140459314,"alleles":["A","G"]},{"alleles":["T","C"],"end":140459316,"feature_type":"variation","strand":1,"source":"dbSNP","start":140459316,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794552605"},{"start":140459318,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AAAA","AA"],"end":140459321,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1443101062","clinical_significance":[]},{"alleles":["AAAATAAAA","AAA"],"end":140459326,"strand":1,"feature_type":"variation","start":140459318,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1216109353","clinical_significance":[]},{"seq_region_name":"7","id":"rs555896026","clinical_significance":[],"alleles":["A","T"],"end":140459319,"strand":1,"feature_type":"variation","start":140459319,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs535696953","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459322,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140459322},{"seq_region_name":"7","id":"rs1241325944","clinical_significance":[],"alleles":["A","G"],"end":140459323,"strand":1,"feature_type":"variation","start":140459323,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1205707726","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["AAAA","-"],"end":140459326,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140459323,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140459326,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459326,"clinical_significance":[],"id":"rs1281839913","seq_region_name":"7"},{"id":"rs1461321105","seq_region_name":"7","clinical_significance":[],"end":140459327,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140459327,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1189760905","clinical_significance":[],"start":140459331,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140459331,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140459332,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140459332,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs994767249"},{"source":"dbSNP","start":140459333,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140459333,"alleles":["T","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs920382248"},{"id":"rs1794553349","seq_region_name":"7","clinical_significance":[],"start":140459337,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140459337,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459339,"feature_type":"variation","strand":1,"end":140459339,"alleles":["A","AA"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794553402"},{"clinical_significance":[],"seq_region_name":"7","id":"rs774079101","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459342,"feature_type":"variation","strand":1,"alleles":["AAAA","AAA"],"end":140459345},{"strand":1,"feature_type":"variation","end":140459343,"alleles":["A","C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140459343,"source":"dbSNP","seq_region_name":"7","id":"rs1047707258","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794553642","alleles":["ACA","A"],"end":140459347,"feature_type":"variation","strand":1,"source":"dbSNP","start":140459345,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1794553703","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140459347,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140459347,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585468119","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459352,"feature_type":"variation","strand":1,"end":140459352,"alleles":["A","G"]},{"source":"dbSNP","start":140459353,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140459353,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1166998015"},{"clinical_significance":[],"seq_region_name":"7","id":"rs886548584","feature_type":"variation","strand":1,"end":140459355,"alleles":["G","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459355},{"end":140459363,"alleles":["AACTAACT","AACT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140459356,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1425487952"},{"end":140459360,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140459360,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794554031"},{"source":"dbSNP","start":140459368,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140459368,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1794554073","seq_region_name":"7"},{"start":140459369,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140459369,"strand":1,"feature_type":"variation","id":"rs1794554152","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140459371,"source":"dbSNP","strand":1,"feature_type":"variation","end":140459371,"alleles":["T","C"],"id":"rs553793568","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","C","T"],"end":140459373,"strand":1,"feature_type":"variation","start":140459373,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1334196471","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140459373,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GAAAGAAAG","GAAAG"],"end":140459381,"seq_region_name":"7","id":"rs1019143269","clinical_significance":[]},{"start":140459377,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140459377,"alleles":["G","T"],"strand":1,"feature_type":"variation","id":"rs1794554450","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794554502","source":"dbSNP","start":140459379,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140459379,"alleles":["A","C"],"feature_type":"variation","strand":1},{"start":140459381,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140459381,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794554565","clinical_significance":[]},{"seq_region_name":"7","id":"rs1047587419","clinical_significance":[],"end":140459383,"alleles":["A","C","T"],"strand":1,"feature_type":"variation","start":140459383,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs2130262456","clinical_significance":[],"start":140459385,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140459385,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"end":140459390,"alleles":["TTTTTT","TTTTTTT"],"strand":1,"feature_type":"variation","start":140459385,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1435738355","clinical_significance":[]},{"end":140459393,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140459393,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1423910661"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459395,"feature_type":"variation","strand":1,"end":140459395,"alleles":["C","A","G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs572172465"},{"feature_type":"variation","strand":1,"end":140459397,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459397,"clinical_significance":[],"seq_region_name":"7","id":"rs1486607580"},{"strand":1,"feature_type":"variation","end":140459401,"alleles":["TGTT","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140459398,"source":"dbSNP","seq_region_name":"7","id":"rs1240019965","clinical_significance":[]},{"end":140459399,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140459399,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs539278992","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1207866143","seq_region_name":"7","feature_type":"variation","strand":1,"end":140459403,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459403},{"clinical_significance":[],"id":"rs1794555088","seq_region_name":"7","feature_type":"variation","strand":1,"end":140459408,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459408},{"end":140459409,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140459409,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1794555153","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140459410,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140459410,"source":"dbSNP","id":"rs1008837205","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459413,"feature_type":"variation","strand":1,"end":140459413,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1040658347"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1221663783","end":140459419,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140459419,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140459420,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140459420,"seq_region_name":"7","id":"rs900416975","clinical_significance":[]},{"id":"rs996840640","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140459421,"source":"dbSNP","strand":1,"feature_type":"variation","end":140459421,"alleles":["T","C","G"]},{"seq_region_name":"7","id":"rs1794555493","clinical_significance":[],"start":140459422,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140459422,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140459433,"alleles":["AAAAAAAAAAAA","AAAAAAAAA","AAAAAAAAAA","AAAAAAAAAAA","AAAAAAAAAAAAA","AAAAAAAAAAAAAA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459422,"clinical_significance":[],"seq_region_name":"7","id":"rs56916081"},{"strand":1,"feature_type":"variation","end":140459423,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140459423,"source":"dbSNP","seq_region_name":"7","id":"rs1794555813","clinical_significance":[]},{"clinical_significance":[],"id":"rs1794555875","seq_region_name":"7","source":"dbSNP","start":140459430,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140459430,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1028261063","clinical_significance":[],"strand":1,"feature_type":"variation","end":140459436,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140459436,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1335286898","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459439,"feature_type":"variation","strand":1,"end":140459439,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1322841471","source":"dbSNP","start":140459443,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140459443,"feature_type":"variation","strand":1},{"id":"rs1261404521","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140459443,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TATCTAT","TAT"],"end":140459449},{"seq_region_name":"7","id":"rs1794556155","clinical_significance":[],"strand":1,"feature_type":"variation","end":140459449,"alleles":["TAT","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140459447,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140459448,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459448,"clinical_significance":[],"seq_region_name":"7","id":"rs1794556208"},{"start":140459449,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A","C"],"end":140459449,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1355633682","clinical_significance":[]},{"end":140459451,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140459451,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1170466647"},{"start":140459455,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140459457,"alleles":["GGG","GG"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794556447","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794556521","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140459457,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459457},{"seq_region_name":"7","id":"rs1794556579","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140459460,"source":"dbSNP","strand":1,"feature_type":"variation","end":140459460,"alleles":["A","G"]},{"clinical_significance":[],"id":"rs1585468324","seq_region_name":"7","source":"dbSNP","start":140459462,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140459462,"alleles":["T","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794556696","source":"dbSNP","start":140459465,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140459465,"alleles":["A","G"],"feature_type":"variation","strand":1},{"id":"rs558210742","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C","T"],"end":140459466,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140459466,"source":"dbSNP"},{"start":140459467,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140459467,"strand":1,"feature_type":"variation","id":"rs1585468335","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140459477,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140459477,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1429839657"},{"clinical_significance":[],"id":"rs1387935150","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459478,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140459478},{"seq_region_name":"7","id":"rs576164073","clinical_significance":[],"alleles":["T","C","G"],"end":140459482,"strand":1,"feature_type":"variation","start":140459482,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1444996252","clinical_significance":[],"strand":1,"feature_type":"variation","end":140459483,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140459483,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1794557180","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140459484,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140459484,"source":"dbSNP"},{"source":"dbSNP","start":140459486,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140459486,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs149357584"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459487,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140459487,"clinical_significance":[],"id":"rs561792441","seq_region_name":"7"},{"start":140459491,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140459491,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1011378527","clinical_significance":[]},{"start":140459494,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140459494,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1022947532","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794557557","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459496,"feature_type":"variation","strand":1,"end":140459497,"alleles":["CA","-"]},{"clinical_significance":[],"id":"rs1794557610","seq_region_name":"7","feature_type":"variation","strand":1,"end":140459498,"alleles":["-","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459499},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140459503,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140459503,"seq_region_name":"7","id":"rs1794557674","clinical_significance":[]},{"clinical_significance":[],"id":"rs1206700431","seq_region_name":"7","source":"dbSNP","start":140459509,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140459509,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs573700676","seq_region_name":"7","source":"dbSNP","start":140459511,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140459511,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1021140260","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140459516,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140459516},{"seq_region_name":"7","id":"rs1794557942","clinical_significance":[],"alleles":["C","T"],"end":140459520,"strand":1,"feature_type":"variation","start":140459520,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs541668641","seq_region_name":"7","source":"dbSNP","start":140459521,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140459521,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140459524,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140459524,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs189123165"},{"clinical_significance":[],"id":"rs1794558151","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459527,"feature_type":"variation","strand":1,"end":140459527,"alleles":["C","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794558209","end":140459528,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140459528,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["G","C"],"end":140459531,"feature_type":"variation","strand":1,"source":"dbSNP","start":140459531,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1794558269","seq_region_name":"7"},{"source":"dbSNP","start":140459532,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140459532,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs982393745","seq_region_name":"7"},{"seq_region_name":"7","id":"rs2130263219","clinical_significance":[],"strand":1,"feature_type":"variation","end":140459535,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140459535,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140459539,"alleles":["AAAAA","AAAAAA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459535,"clinical_significance":[],"id":"rs2130263230","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1313293058","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140459538,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459538},{"alleles":["A","G"],"end":140459539,"feature_type":"variation","strand":1,"source":"dbSNP","start":140459539,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130263255"},{"source":"dbSNP","start":140459543,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["CC","C"],"end":140459544,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130263268"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1395826028","alleles":["A","G"],"end":140459548,"feature_type":"variation","strand":1,"source":"dbSNP","start":140459548,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140459551,"source":"dbSNP","strand":1,"feature_type":"variation","end":140459551,"alleles":["C","G"],"seq_region_name":"7","id":"rs1031324194","clinical_significance":[]},{"source":"dbSNP","start":140459553,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140459573,"alleles":["ATCTGTAAATCTTAGGTAATC","ATC"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1173736538"},{"feature_type":"variation","strand":1,"alleles":["-","CAAA"],"end":140459563,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459564,"clinical_significance":[],"seq_region_name":"7","id":"rs2130263316"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140459567,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140459567,"seq_region_name":"7","id":"rs1463044378","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs955813110","end":140459571,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140459571,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140459573,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459573,"clinical_significance":[],"seq_region_name":"7","id":"rs1167442764"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140459574,"source":"dbSNP","strand":1,"feature_type":"variation","end":140459574,"alleles":["C","T"],"seq_region_name":"7","id":"rs992570751","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1457270302","feature_type":"variation","strand":1,"end":140459585,"alleles":["TAAAGTA","TA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459579},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459580,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140459580,"clinical_significance":[],"seq_region_name":"7","id":"rs1794558857"},{"source":"dbSNP","start":140459583,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140459583,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794558913"},{"strand":1,"feature_type":"variation","end":140459584,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140459584,"source":"dbSNP","seq_region_name":"7","id":"rs1794558975","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1160247106","source":"dbSNP","start":140459585,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140459585,"alleles":["A","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1794559079","seq_region_name":"7","alleles":["T","C"],"end":140459587,"feature_type":"variation","strand":1,"source":"dbSNP","start":140459587,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs2130263447","clinical_significance":[],"strand":1,"feature_type":"variation","end":140459588,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140459588,"source":"dbSNP"},{"seq_region_name":"7","id":"rs80206917","clinical_significance":[],"start":140459589,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140459589,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140459592,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459592,"clinical_significance":[],"seq_region_name":"7","id":"rs948535588"},{"clinical_significance":[],"id":"rs1794559315","seq_region_name":"7","feature_type":"variation","strand":1,"end":140459595,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459595},{"strand":1,"feature_type":"variation","end":140459599,"alleles":["A","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140459599,"source":"dbSNP","seq_region_name":"7","id":"rs1178917643","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459600,"feature_type":"variation","strand":1,"end":140459600,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs959609669"},{"clinical_significance":[],"seq_region_name":"7","id":"rs551713759","source":"dbSNP","start":140459602,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140459602,"alleles":["C","A","G"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459611,"feature_type":"variation","strand":1,"end":140459611,"alleles":["G","A"],"clinical_significance":[],"id":"rs564152079","seq_region_name":"7"},{"id":"rs1400013510","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140459615,"source":"dbSNP","strand":1,"feature_type":"variation","end":140459615,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs1324045861","clinical_significance":[],"start":140459616,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140459616,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"start":140459618,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140459618,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1347151065","clinical_significance":[]},{"start":140459619,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C"],"end":140459619,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1407009722","clinical_significance":[]},{"source":"dbSNP","start":140459621,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140459621,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs980054952"},{"id":"rs2130263661","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140459622,"source":"dbSNP","strand":1,"feature_type":"variation","end":140459622,"alleles":["G","A"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459626,"feature_type":"variation","strand":1,"end":140459629,"alleles":["GGGG","GGG"],"clinical_significance":[],"id":"rs920537117","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1229032527","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140459629,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140459629},{"seq_region_name":"7","id":"rs1289945243","clinical_significance":[],"alleles":["A","G"],"end":140459630,"strand":1,"feature_type":"variation","start":140459630,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs547680236","end":140459632,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140459632,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140459634,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140459634,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1047757397","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140459635,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459635,"clinical_significance":[],"seq_region_name":"7","id":"rs544776665"},{"source":"dbSNP","start":140459635,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140459657,"alleles":["TGTCAAAACTAAGCAAATGGATG","TGTCAAAACTAAGCAAATGGATGTCAAAACTAAGCAAATGGATG"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1309762679","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1794560470","clinical_significance":[],"start":140459645,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140459645,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140459647,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140459647,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1794560542","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs144723210","source":"dbSNP","start":140459651,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140459651,"alleles":["A","G"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459652,"feature_type":"variation","strand":1,"end":140459652,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs549908504"},{"start":140459653,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140459653,"strand":1,"feature_type":"variation","id":"rs1794560729","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459654,"feature_type":"variation","strand":1,"end":140459654,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794560819"},{"feature_type":"variation","strand":1,"alleles":["-","TATACTTTAAATACGTGCAGTCTAT"],"end":140459654,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459655,"clinical_significance":[],"seq_region_name":"7","id":"rs1794560870"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1405757831","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140459656,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459656},{"source":"dbSNP","start":140459657,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140459657,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs747436440"},{"seq_region_name":"7","id":"rs1469187590","clinical_significance":[],"start":140459658,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140459658,"strand":1,"feature_type":"variation"},{"start":140459662,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140459662,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs148103767","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140459663,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140459663,"id":"rs776851592","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs745881907","seq_region_name":"7","feature_type":"variation","strand":1,"end":140459666,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459666},{"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140459667,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459667,"clinical_significance":[],"seq_region_name":"7","id":"rs73485155"},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140459668,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140459668,"source":"dbSNP","id":"rs1794561403","seq_region_name":"7","clinical_significance":[]},{"end":140459671,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140459671,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs775606693"},{"clinical_significance":[],"seq_region_name":"7","id":"rs750032927","feature_type":"variation","strand":1,"alleles":["CCC","CCCC"],"end":140459673,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459671},{"end":140459673,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140459673,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1794561585","seq_region_name":"7"},{"alleles":["CTAACT","CT"],"end":140459680,"feature_type":"variation","strand":1,"source":"dbSNP","start":140459675,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs760443771","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140459682,"alleles":["CTCT","CT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459679,"clinical_significance":[],"seq_region_name":"7","id":"rs1418810979"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140459682,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459682,"clinical_significance":[],"seq_region_name":"7","id":"rs1476973001"},{"clinical_significance":[],"seq_region_name":"7","id":"rs761623460","source":"dbSNP","start":140459685,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140459685,"feature_type":"variation","strand":1},{"alleles":["T","C","G"],"end":140459688,"strand":1,"feature_type":"variation","start":140459688,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs767520106","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140459690,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140459690,"source":"dbSNP","seq_region_name":"7","id":"rs772834153","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1190365383","source":"dbSNP","start":140459691,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140459691,"alleles":["T","A"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459693,"feature_type":"variation","strand":1,"alleles":["TTCAG","-"],"end":140459697,"clinical_significance":[],"seq_region_name":"7","id":"rs1161046684"},{"clinical_significance":[],"seq_region_name":"7","id":"rs760531744","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459695,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140459695},{"seq_region_name":"7","id":"rs1022451597","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140459707,"source":"dbSNP","strand":1,"feature_type":"variation","end":140459707,"alleles":["T","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs765877418","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459709,"feature_type":"variation","strand":1,"end":140459709,"alleles":["C","T"]},{"clinical_significance":[],"id":"rs1156830668","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140459716,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459716},{"clinical_significance":[],"id":"rs1250989492","seq_region_name":"7","end":140459717,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140459717,"consequence_type":"synonymous_variant","assembly_name":"GRCh38"},{"clinical_significance":["uncertain significance"],"seq_region_name":"7","id":"rs201667171","end":140459721,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140459721,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140459723,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","end":140459723,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs374250184","seq_region_name":"7"},{"seq_region_name":"7","id":"rs759317398","clinical_significance":[],"end":140459725,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140459725,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"seq_region_name":"7","id":"rs1329510579","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140459729,"source":"dbSNP","strand":1,"feature_type":"variation","end":140459729,"alleles":["A","G","T"]},{"end":140459743,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140459743,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":["uncertain significance"],"id":"rs944506546","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1280469005","clinical_significance":[],"start":140459745,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140459745,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs764816106","source":"dbSNP","start":140459758,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140459758,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs142029587","seq_region_name":"7","end":140459762,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140459762,"consequence_type":"synonymous_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs765950692","seq_region_name":"7","source":"dbSNP","start":140459765,"consequence_type":"inframe_insertion","assembly_name":"GRCh38","end":140459783,"alleles":["ACCTGCTCCTACAGTTGCA","ACCTGCTCCTACAGTTGCACCTGCTCCTACAGTTGCA"],"feature_type":"variation","strand":1},{"end":140459766,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140459766,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs758795023","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1040202016","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140459767,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459767},{"alleles":["C","T"],"end":140459770,"strand":1,"feature_type":"variation","start":140459770,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs900448073","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140459774,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459774,"clinical_significance":[],"seq_region_name":"7","id":"rs1360804191"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140459776,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459776,"clinical_significance":[],"seq_region_name":"7","id":"rs1222516398"},{"seq_region_name":"7","id":"rs150662826","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140459777,"source":"dbSNP","strand":1,"feature_type":"variation","end":140459777,"alleles":["A","T"]},{"end":140459778,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140459778,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs1348073506","clinical_significance":[]},{"seq_region_name":"7","id":"rs753285484","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"inframe_insertion","start":140459781,"source":"dbSNP","strand":1,"feature_type":"variation","end":140459783,"alleles":["GCA","GCAGCA"]},{"source":"dbSNP","start":140459782,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140459782,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs373946584"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1329012091","end":140459786,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140459786,"consequence_type":"synonymous_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs539604836","feature_type":"variation","strand":1,"end":140459789,"alleles":["T","C"],"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459789},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140459791,"source":"dbSNP","strand":1,"feature_type":"variation","end":140459791,"alleles":["A","G"],"seq_region_name":"7","id":"rs781604828","clinical_significance":[]},{"end":140459792,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140459792,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs746078950","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140459801,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459801,"clinical_significance":[],"id":"rs375505852","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140459804,"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140459804,"source":"dbSNP","id":"rs1794564630","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs780067452","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140459806,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140459806},{"strand":1,"feature_type":"variation","end":140459809,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140459809,"source":"dbSNP","id":"rs893783011","seq_region_name":"7","clinical_significance":["uncertain significance"]},{"feature_type":"variation","strand":1,"end":140459810,"alleles":["G","A","T"],"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459810,"clinical_significance":[],"id":"rs749407952","seq_region_name":"7"},{"id":"rs141902077","seq_region_name":"7","clinical_significance":["uncertain significance"],"alleles":["C","T"],"end":140459811,"strand":1,"feature_type":"variation","start":140459811,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"source":"dbSNP","start":140459813,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140459813,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs760593670","seq_region_name":"7"},{"seq_region_name":"7","id":"rs371705983","clinical_significance":["uncertain significance"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140459814,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140459814},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130264903","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140459815,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459815},{"strand":1,"feature_type":"variation","end":140459817,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140459817,"source":"dbSNP","seq_region_name":"7","id":"rs1035168824","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1444947178","source":"dbSNP","start":140459819,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140459819,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1309010037","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140459822,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459822},{"alleles":["C","G","T"],"end":140459827,"strand":1,"feature_type":"variation","start":140459827,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs1290341425","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs776615097","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459829,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140459829},{"seq_region_name":"7","id":"rs1455499317","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140459830,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140459830,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140459831,"alleles":["T","C","G"],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140459831,"source":"dbSNP","id":"rs759235639","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1043776","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459833,"feature_type":"variation","strand":1,"end":140459833,"alleles":["G","A","T"]},{"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140459837,"source":"dbSNP","strand":1,"feature_type":"variation","end":140459837,"alleles":["A","G"],"seq_region_name":"7","id":"rs752103170","clinical_significance":[]},{"end":140459840,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140459840,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs762542342"},{"id":"rs1481448642","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140459841,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140459841},{"clinical_significance":[],"id":"rs764441476","seq_region_name":"7","end":140459842,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140459842,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs143237010","consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459843,"feature_type":"variation","strand":1,"end":140459843,"alleles":["C","T"]},{"strand":1,"feature_type":"variation","end":140459844,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140459844,"source":"dbSNP","seq_region_name":"7","id":"rs991043337","clinical_significance":[]},{"id":"rs1198291212","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"frameshift_variant","start":140459844,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","-"],"end":140459844},{"assembly_name":"GRCh38","consequence_type":"inframe_deletion","start":140459844,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GATGA","GA"],"end":140459848,"id":"rs983295375","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","C"],"end":140459847,"strand":1,"feature_type":"variation","start":140459847,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"stop_gained","seq_region_name":"7","id":"rs1794566897","clinical_significance":[]},{"id":"rs907882323","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140459848,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140459848,"source":"dbSNP"},{"clinical_significance":[],"id":"rs757764783","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140459849,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459849},{"end":140459851,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140459851,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs1207201081","clinical_significance":[]},{"alleles":["C","T"],"end":140459853,"feature_type":"variation","strand":1,"source":"dbSNP","start":140459853,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1196474004"},{"clinical_significance":[],"seq_region_name":"7","id":"rs781516749","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459860,"feature_type":"variation","strand":1,"end":140459860,"alleles":["A","C"]},{"source":"dbSNP","start":140459865,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140459865,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1335984362"},{"strand":1,"feature_type":"variation","end":140459866,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140459866,"source":"dbSNP","seq_region_name":"7","id":"rs1461686497","clinical_significance":[]},{"seq_region_name":"7","id":"rs1185393767","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140459869,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140459869,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"frameshift_variant","start":140459869,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GGG","GG"],"end":140459871,"seq_region_name":"7","id":"rs944683876","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140459870,"alleles":["G","A"],"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459870,"clinical_significance":[],"seq_region_name":"7","id":"rs750815147"},{"strand":1,"feature_type":"variation","end":140459871,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140459871,"source":"dbSNP","id":"rs756278638","seq_region_name":"7","clinical_significance":["uncertain significance"]},{"feature_type":"variation","strand":1,"end":140459874,"alleles":["G","A"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459874,"clinical_significance":[],"seq_region_name":"7","id":"rs147474750"},{"seq_region_name":"7","id":"rs1272529518","clinical_significance":[],"start":140459876,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","alleles":["C","T"],"end":140459876,"strand":1,"feature_type":"variation"},{"id":"rs749260304","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140459878,"strand":1,"feature_type":"variation","start":140459878,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs768773376","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459880,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140459880},{"id":"rs778914723","seq_region_name":"7","clinical_significance":[],"start":140459882,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","alleles":["A","T"],"end":140459882,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1794568880","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140459883,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140459883},{"feature_type":"variation","strand":1,"end":140459885,"alleles":["T","C"],"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459885,"clinical_significance":[],"seq_region_name":"7","id":"rs1794568977"},{"alleles":["T","C"],"end":140459891,"strand":1,"feature_type":"variation","start":140459891,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","seq_region_name":"7","id":"rs1794569069","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140459895,"alleles":["G","A","C"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459895,"clinical_significance":[],"seq_region_name":"7","id":"rs746939657"},{"strand":1,"feature_type":"variation","end":140459899,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140459899,"source":"dbSNP","seq_region_name":"7","id":"rs771029713","clinical_significance":["uncertain significance"]},{"strand":1,"feature_type":"variation","end":140459901,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140459901,"source":"dbSNP","id":"rs1455032685","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs776529554","clinical_significance":[],"alleles":["C","T"],"end":140459909,"strand":1,"feature_type":"variation","start":140459909,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant"},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459910,"feature_type":"variation","strand":1,"end":140459910,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1338188113"},{"clinical_significance":[],"seq_region_name":"7","id":"rs745683076","end":140459917,"alleles":["A","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140459917,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1387699031","clinical_significance":[],"end":140459919,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140459919,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"id":"rs10243155","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140459921,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140459921},{"seq_region_name":"7","id":"rs775217973","clinical_significance":[],"start":140459922,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["T","A"],"end":140459922,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs762583662","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459925,"feature_type":"variation","strand":1,"end":140459925,"alleles":["C","T"]},{"alleles":["T","C","G"],"end":140459926,"strand":1,"feature_type":"variation","start":140459926,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs1257165153","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1461646032","feature_type":"variation","strand":1,"end":140459927,"alleles":["A","G"],"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459927},{"start":140459931,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["T","C"],"end":140459931,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs932069543","clinical_significance":[]},{"id":"rs1205474383","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140459934,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140459934,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140459935,"source":"dbSNP","strand":1,"feature_type":"variation","end":140459935,"alleles":["A","T"],"seq_region_name":"7","id":"rs1253907200","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130265957","end":140459937,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140459937,"consequence_type":"splice_acceptor_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1441788129","source":"dbSNP","start":140459938,"consequence_type":"splice_acceptor_variant","assembly_name":"GRCh38","end":140459938,"alleles":["T","TGCAGCGGTCTCCAT"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1193935703","clinical_significance":[],"strand":1,"feature_type":"variation","end":140459940,"alleles":["-","ATACAGTACCCTCGCT"],"assembly_name":"GRCh38","consequence_type":"splice_region_variant","start":140459941,"source":"dbSNP"},{"id":"rs1563088722","seq_region_name":"7","clinical_significance":[],"end":140459945,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140459945,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_polypyrimidine_tract_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs763649783","source":"dbSNP","start":140459946,"consequence_type":"splice_polypyrimidine_tract_variant","assembly_name":"GRCh38","end":140459946,"alleles":["A","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs773784995","source":"dbSNP","start":140459949,"consequence_type":"splice_polypyrimidine_tract_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140459949,"feature_type":"variation","strand":1},{"consequence_type":"splice_polypyrimidine_tract_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459951,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140459951,"clinical_significance":[],"seq_region_name":"7","id":"rs1563088732"},{"assembly_name":"GRCh38","consequence_type":"splice_polypyrimidine_tract_variant","start":140459953,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140459953,"seq_region_name":"7","id":"rs1170298403","clinical_significance":[]},{"seq_region_name":"7","id":"rs369870679","clinical_significance":[],"alleles":["T","C"],"end":140459956,"strand":1,"feature_type":"variation","start":140459956,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140459958,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140459958,"alleles":["A","T"],"strand":1,"feature_type":"variation","id":"rs1794571038","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140459958,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AG","-"],"end":140459959,"seq_region_name":"7","id":"rs1471199375","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140459960,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140459960,"source":"dbSNP","seq_region_name":"7","id":"rs373210739","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140459962,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459962,"clinical_significance":[],"seq_region_name":"7","id":"rs1563088753"},{"strand":1,"feature_type":"variation","end":140459963,"alleles":["-","ATA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140459964,"source":"dbSNP","id":"rs1563088756","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140459964,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140459964,"source":"dbSNP","seq_region_name":"7","id":"rs750725003","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs183792436","alleles":["G","A","T"],"end":140459965,"feature_type":"variation","strand":1,"source":"dbSNP","start":140459965,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140459966,"alleles":["GG","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459965,"clinical_significance":[],"seq_region_name":"7","id":"rs1794571577"},{"strand":1,"feature_type":"variation","end":140459966,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140459966,"source":"dbSNP","id":"rs1244073811","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459967,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140459967,"clinical_significance":[],"seq_region_name":"7","id":"rs754076348"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459969,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140459969,"clinical_significance":[],"seq_region_name":"7","id":"rs1563088773"},{"seq_region_name":"7","id":"rs377447350","clinical_significance":[],"start":140459970,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C"],"end":140459970,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459971,"feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140459971,"clinical_significance":[],"seq_region_name":"7","id":"rs1441119681"},{"source":"dbSNP","start":140459972,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140459972,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs375808428"},{"seq_region_name":"7","id":"rs188671896","clinical_significance":[],"strand":1,"feature_type":"variation","end":140459973,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140459973,"source":"dbSNP"},{"end":140459975,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140459975,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs781292987"},{"clinical_significance":[],"seq_region_name":"7","id":"rs745592796","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140459976,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459976},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563088789","end":140459977,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140459977,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs769712965","clinical_significance":[],"strand":1,"feature_type":"variation","end":140459979,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140459979,"source":"dbSNP"},{"start":140459981,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140459981,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs975914983","clinical_significance":[]},{"seq_region_name":"7","id":"rs775210420","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140459982,"source":"dbSNP","strand":1,"feature_type":"variation","end":140459982,"alleles":["C","A"]},{"id":"rs1794572469","seq_region_name":"7","clinical_significance":[],"start":140459983,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140459983,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140459984,"source":"dbSNP","strand":1,"feature_type":"variation","end":140459984,"alleles":["A","C","T"],"seq_region_name":"7","id":"rs1205689882","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs748950871","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140459986,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459986},{"seq_region_name":"7","id":"rs1487383178","clinical_significance":[],"alleles":["T","A"],"end":140459988,"strand":1,"feature_type":"variation","start":140459988,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140459991,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140459991,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1794572695","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794572752","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459993,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140459993},{"clinical_significance":[],"id":"rs1339535910","seq_region_name":"7","feature_type":"variation","strand":1,"end":140459994,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459994},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140459998,"feature_type":"variation","strand":1,"alleles":["A","C","G","T"],"end":140459998,"clinical_significance":[],"id":"rs11763850","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460001,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140460001,"seq_region_name":"7","id":"rs2130266578","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460002,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140460002,"clinical_significance":[],"id":"rs1225672999","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1054261160","clinical_significance":[],"strand":1,"feature_type":"variation","end":140460003,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460003,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585469598","end":140460009,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140460009,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460011,"source":"dbSNP","strand":1,"feature_type":"variation","end":140460011,"alleles":["C","A"],"seq_region_name":"7","id":"rs1315399997","clinical_significance":[]},{"start":140460015,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C"],"end":140460015,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1449970396","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460016,"source":"dbSNP","strand":1,"feature_type":"variation","end":140460016,"alleles":["G","A"],"seq_region_name":"7","id":"rs893815581","clinical_significance":[]},{"source":"dbSNP","start":140460018,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140460018,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1794573407","seq_region_name":"7"},{"start":140460021,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140460021,"strand":1,"feature_type":"variation","id":"rs2130266683","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs778192528","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460023,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140460023},{"clinical_significance":[],"seq_region_name":"7","id":"rs1442678502","end":140460026,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140460026,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460029,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140460029,"clinical_significance":[],"seq_region_name":"7","id":"rs140930652"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1398788709","feature_type":"variation","strand":1,"alleles":["AGAGAG","AGAG"],"end":140460035,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460030},{"source":"dbSNP","start":140460031,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140460031,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1166818093","seq_region_name":"7"},{"seq_region_name":"7","id":"rs902620573","clinical_significance":[],"start":140460036,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C","T"],"end":140460036,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460037,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140460037,"clinical_significance":[],"seq_region_name":"7","id":"rs1386097830"},{"seq_region_name":"7","id":"rs191927030","clinical_significance":[],"alleles":["T","G"],"end":140460038,"strand":1,"feature_type":"variation","start":140460038,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1023955546","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460039,"source":"dbSNP","strand":1,"feature_type":"variation","end":140460041,"alleles":["GGG","GG"]},{"end":140460041,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140460041,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs970250825"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1237384711","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140460044,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460044},{"end":140460046,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140460046,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1003619185","clinical_significance":[]},{"seq_region_name":"7","id":"rs1001281937","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460047,"source":"dbSNP","strand":1,"feature_type":"variation","end":140460047,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1585469702","clinical_significance":[],"start":140460050,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140460050,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1035201350","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140460051,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460051,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1462696637","source":"dbSNP","start":140460053,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140460053,"alleles":["A","G"],"feature_type":"variation","strand":1},{"alleles":["C","G"],"end":140460056,"feature_type":"variation","strand":1,"source":"dbSNP","start":140460056,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1794574476","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140460057,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460057,"source":"dbSNP","seq_region_name":"7","id":"rs1794574535","clinical_significance":[]},{"id":"rs184483440","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460061,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140460061},{"seq_region_name":"7","id":"rs1202415851","clinical_significance":[],"strand":1,"feature_type":"variation","end":140460063,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460063,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140460064,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460064,"clinical_significance":[],"seq_region_name":"7","id":"rs1012508744"},{"seq_region_name":"7","id":"rs1394459993","clinical_significance":[],"strand":1,"feature_type":"variation","end":140460065,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460065,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140460069,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460069,"source":"dbSNP","seq_region_name":"7","id":"rs2130266965","clinical_significance":[]},{"source":"dbSNP","start":140460070,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140460070,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1390843447"},{"id":"rs1585469750","seq_region_name":"7","clinical_significance":[],"end":140460074,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140460074,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["C","G"],"end":140460076,"feature_type":"variation","strand":1,"source":"dbSNP","start":140460076,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs563828672"},{"seq_region_name":"7","id":"rs768236232","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460077,"source":"dbSNP","strand":1,"feature_type":"variation","end":140460077,"alleles":["C","T"]},{"clinical_significance":[],"id":"rs773859209","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460078,"feature_type":"variation","strand":1,"end":140460078,"alleles":["G","A"]},{"clinical_significance":[],"id":"rs1794575217","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460079,"feature_type":"variation","strand":1,"end":140460079,"alleles":["T","A"]},{"seq_region_name":"7","id":"rs761322307","clinical_significance":[],"alleles":["C","T"],"end":140460082,"strand":1,"feature_type":"variation","start":140460082,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1377462407","clinical_significance":[],"start":140460083,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140460083,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460085,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","G","T"],"end":140460085,"id":"rs1454741268","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140460090,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460090,"clinical_significance":[],"seq_region_name":"7","id":"rs1794575491"},{"id":"rs1283502465","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460091,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140460091},{"clinical_significance":[],"id":"rs531140498","seq_region_name":"7","end":140460092,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140460092,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs564142443","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460093,"source":"dbSNP","strand":1,"feature_type":"variation","end":140460093,"alleles":["G","A","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563088895","source":"dbSNP","start":140460098,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140460098,"feature_type":"variation","strand":1},{"start":140460103,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140460103,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs767942387","clinical_significance":[]},{"seq_region_name":"7","id":"rs773700099","clinical_significance":[],"strand":1,"feature_type":"variation","end":140460104,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460104,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140460105,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460105,"clinical_significance":[],"seq_region_name":"7","id":"rs1345699952"},{"id":"rs761228073","seq_region_name":"7","clinical_significance":[],"end":140460106,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140460106,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130267278","feature_type":"variation","strand":1,"end":140460108,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460108},{"seq_region_name":"7","id":"rs543511060","clinical_significance":[],"strand":1,"feature_type":"variation","end":140460110,"alleles":["A","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460110,"source":"dbSNP"},{"id":"rs561788981","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140460111,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460111,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460112,"source":"dbSNP","strand":1,"feature_type":"variation","end":140460112,"alleles":["G","A"],"id":"rs1794576252","seq_region_name":"7","clinical_significance":[]},{"start":140460113,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140460113,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs907770522","clinical_significance":[]},{"source":"dbSNP","start":140460114,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140460114,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794576404"},{"start":140460117,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140460117,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs548438129","clinical_significance":[]},{"id":"rs1351426472","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140460118,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460118,"source":"dbSNP"},{"id":"rs377148562","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460121,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140460121},{"id":"rs1215913060","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140460122,"alleles":["C","A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460122,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1243531490","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140460123,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460123},{"source":"dbSNP","start":140460125,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140460125,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1563088920"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140460133,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460133,"source":"dbSNP","seq_region_name":"7","id":"rs1292629240","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140460136,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460136,"clinical_significance":[],"seq_region_name":"7","id":"rs1489570697"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1159543457","feature_type":"variation","strand":1,"end":140460138,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460138},{"seq_region_name":"7","id":"rs1208336189","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460139,"source":"dbSNP","strand":1,"feature_type":"variation","end":140460139,"alleles":["C","G","T"]},{"strand":1,"feature_type":"variation","end":140460140,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460140,"source":"dbSNP","id":"rs190090121","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs58076938","clinical_significance":[],"end":140460142,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140460142,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["A","G"],"end":140460143,"feature_type":"variation","strand":1,"source":"dbSNP","start":140460143,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794577302"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460145,"source":"dbSNP","strand":1,"feature_type":"variation","end":140460145,"alleles":["G","T"],"seq_region_name":"7","id":"rs1224895019","clinical_significance":[]},{"id":"rs1180902543","seq_region_name":"7","clinical_significance":[],"start":140460146,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140460146,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1378941448","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140460147,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460147,"source":"dbSNP"},{"alleles":["G","C"],"end":140460151,"feature_type":"variation","strand":1,"source":"dbSNP","start":140460151,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1439642631"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460152,"source":"dbSNP","strand":1,"feature_type":"variation","end":140460152,"alleles":["T","C","G"],"id":"rs752768755","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1365707993","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460157,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140460157},{"seq_region_name":"7","id":"rs1288830596","clinical_significance":[],"start":140460160,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140460160,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"alleles":["C","A"],"end":140460161,"feature_type":"variation","strand":1,"source":"dbSNP","start":140460161,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1224130890","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140460163,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460163,"clinical_significance":[],"seq_region_name":"7","id":"rs1459104584"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1291491488","alleles":["T","A"],"end":140460164,"feature_type":"variation","strand":1,"source":"dbSNP","start":140460164,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140460165,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140460165,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs921770216"},{"seq_region_name":"7","id":"rs1389745750","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140460166,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460166,"source":"dbSNP"},{"id":"rs1284143196","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140460168,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460168,"source":"dbSNP"},{"source":"dbSNP","start":140460172,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140460172,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs931781138"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1346288862","source":"dbSNP","start":140460174,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140460174,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460175,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140460175,"clinical_significance":[],"seq_region_name":"7","id":"rs1311203751"},{"source":"dbSNP","start":140460176,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140460176,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794578196"},{"id":"rs1563088979","seq_region_name":"7","clinical_significance":[],"start":140460177,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["ACA","A"],"end":140460179,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs989934098","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460178,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140460178},{"id":"rs1349522386","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460187,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140460187},{"end":140460188,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140460188,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1374508340","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1239385336","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460190,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140460190},{"clinical_significance":[],"seq_region_name":"7","id":"rs1459210493","feature_type":"variation","strand":1,"end":140460191,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460191},{"clinical_significance":[],"id":"rs1315793821","seq_region_name":"7","alleles":["A","T"],"end":140460192,"feature_type":"variation","strand":1,"source":"dbSNP","start":140460192,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs565955446","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460195,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140460195},{"feature_type":"variation","strand":1,"end":140460196,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460196,"clinical_significance":[],"id":"rs1323640828","seq_region_name":"7"},{"seq_region_name":"7","id":"rs532061767","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460196,"source":"dbSNP","strand":1,"feature_type":"variation","end":140460199,"alleles":["GAGA","GA"]},{"start":140460198,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140460198,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1242875020","clinical_significance":[]},{"start":140460203,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140460203,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1265011235","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140460204,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460204,"clinical_significance":[],"seq_region_name":"7","id":"rs1481088782"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460205,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140460205,"clinical_significance":[],"seq_region_name":"7","id":"rs1245781173"},{"seq_region_name":"7","id":"rs1794579181","clinical_significance":[],"alleles":["T","C"],"end":140460209,"strand":1,"feature_type":"variation","start":140460209,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140460212,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140460212,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1200857101"},{"id":"rs1794579307","seq_region_name":"7","clinical_significance":[],"start":140460213,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140460213,"strand":1,"feature_type":"variation"},{"end":140460214,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140460214,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585470114"},{"seq_region_name":"7","id":"rs1794579419","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140460219,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460219,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140460221,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460221,"clinical_significance":[],"seq_region_name":"7","id":"rs1585470121"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460223,"source":"dbSNP","strand":1,"feature_type":"variation","end":140460223,"alleles":["G","A"],"id":"rs1236770030","seq_region_name":"7","clinical_significance":[]},{"id":"rs1457689068","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460224,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140460224},{"seq_region_name":"7","id":"rs533122979","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140460225,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460225,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140460226,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460226,"clinical_significance":[],"id":"rs13312139","seq_region_name":"7"},{"start":140460228,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140460228,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1324234761","clinical_significance":[]},{"source":"dbSNP","start":140460229,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","AA"],"end":140460229,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794579874"},{"source":"dbSNP","start":140460229,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AGAG","AG"],"end":140460232,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1425108156"},{"seq_region_name":"7","id":"rs1217560312","clinical_significance":[],"start":140460232,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140460232,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1162097139","clinical_significance":[],"start":140460233,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140460233,"alleles":["T","C","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1367474510","clinical_significance":[],"strand":1,"feature_type":"variation","end":140460234,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460234,"source":"dbSNP"},{"source":"dbSNP","start":140460236,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140460236,"alleles":["G","A","C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1794580214","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1462200252","source":"dbSNP","start":140460239,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140460239,"alleles":["T","-"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140460239,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460239,"clinical_significance":[],"seq_region_name":"7","id":"rs1585470200"},{"feature_type":"variation","strand":1,"end":140460240,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460240,"clinical_significance":[],"seq_region_name":"7","id":"rs1271061143"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1333080520","source":"dbSNP","start":140460241,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140460241,"alleles":["C","T"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460242,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140460242,"seq_region_name":"7","id":"rs1453823582","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130268802","source":"dbSNP","start":140460243,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TCTC","TC"],"end":140460246,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1397905745","clinical_significance":[],"start":140460244,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","T"],"end":140460244,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140460247,"alleles":["CTCA","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460244,"source":"dbSNP","id":"rs1794580654","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1794580711","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["CTCAA","-"],"end":140460248,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460244},{"clinical_significance":[],"id":"rs1180195794","seq_region_name":"7","source":"dbSNP","start":140460245,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140460245,"alleles":["T","A"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["T","-"],"end":140460245,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460245,"source":"dbSNP","seq_region_name":"7","id":"rs1794580809","clinical_significance":[]},{"seq_region_name":"7","id":"rs1563089043","clinical_significance":[],"end":140460249,"alleles":["TCAAA","-"],"strand":1,"feature_type":"variation","start":140460245,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460246,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["-","A","AA"],"end":140460245,"seq_region_name":"7","id":"rs1794580979","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460246,"source":"dbSNP","strand":1,"feature_type":"variation","end":140460246,"alleles":["C","A"],"seq_region_name":"7","id":"rs1251511721","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","-"],"end":140460246,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460246,"source":"dbSNP","seq_region_name":"7","id":"rs1320331090","clinical_significance":[]},{"source":"dbSNP","start":140460246,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["CA","-"],"end":140460247,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794581162"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460246,"source":"dbSNP","strand":1,"feature_type":"variation","end":140460249,"alleles":["CAAA","-"],"id":"rs1563089053","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs548142366","alleles":["CAAAA","-"],"end":140460250,"feature_type":"variation","strand":1,"source":"dbSNP","start":140460246,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460246,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CAAAAA","-"],"end":140460251,"seq_region_name":"7","id":"rs1563089059","clinical_significance":[]},{"seq_region_name":"7","id":"rs1445938329","clinical_significance":[],"strand":1,"feature_type":"variation","end":140460247,"alleles":["A","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460247,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1794581449","clinical_significance":[],"start":140460247,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140460251,"alleles":["AAAAA","AAAAAGAAAAAAAAAAAAA"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs58698651","clinical_significance":[],"alleles":["AAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAA","AAAAAAAAAAA","AAAAAAAAAAAA","AAAAAAAAAAAAA","AAAAAAAAAAAAAA","AAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA"],"end":140460267,"strand":1,"feature_type":"variation","start":140460247,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1417747541","source":"dbSNP","start":140460249,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140460249,"alleles":["A","C"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140460250,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460250,"source":"dbSNP","seq_region_name":"7","id":"rs1174980916","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794582278","alleles":["A","C"],"end":140460251,"feature_type":"variation","strand":1,"source":"dbSNP","start":140460251,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1375462626","seq_region_name":"7","clinical_significance":[],"start":140460256,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140460267,"alleles":["AAAAAAAAAAAA","AAAAAAAAAAAAAAAAACAAAAAAAAAAAA"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs2130269305","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460260,"source":"dbSNP","strand":1,"feature_type":"variation","end":140460260,"alleles":["A","AGA"]},{"strand":1,"feature_type":"variation","end":140460262,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460262,"source":"dbSNP","seq_region_name":"7","id":"rs1794582399","clinical_significance":[]},{"start":140460266,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140460266,"strand":1,"feature_type":"variation","id":"rs1395154033","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1794582516","seq_region_name":"7","alleles":["A","G","T"],"end":140460267,"feature_type":"variation","strand":1,"source":"dbSNP","start":140460267,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1381948850","seq_region_name":"7","clinical_significance":[],"end":140460267,"alleles":["-","T"],"strand":1,"feature_type":"variation","start":140460268,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1331788274","seq_region_name":"7","alleles":["G","-"],"end":140460268,"feature_type":"variation","strand":1,"source":"dbSNP","start":140460268,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1337384528","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460268,"source":"dbSNP","strand":1,"feature_type":"variation","end":140460268,"alleles":["G","A","C","T"]},{"start":140460269,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140460269,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1443356756","clinical_significance":[]},{"clinical_significance":[],"id":"rs1794582845","seq_region_name":"7","source":"dbSNP","start":140460271,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140460271,"alleles":["A","G"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140460279,"alleles":["GCACTCAC","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460272,"source":"dbSNP","seq_region_name":"7","id":"rs2130269484","clinical_significance":[]},{"id":"rs1794582907","seq_region_name":"7","clinical_significance":[],"alleles":["C","A"],"end":140460273,"strand":1,"feature_type":"variation","start":140460273,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585470337","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460274,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140460274},{"start":140460276,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140460276,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1358026428","clinical_significance":[]},{"clinical_significance":[],"id":"rs1794583041","seq_region_name":"7","end":140460277,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140460277,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140460278,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460278,"source":"dbSNP","id":"rs1585470343","seq_region_name":"7","clinical_significance":[]},{"start":140460279,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140460284,"alleles":["CTGCCT","-"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130269585","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585470346","clinical_significance":[],"strand":1,"feature_type":"variation","end":140460281,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460281,"source":"dbSNP"},{"start":140460282,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","T"],"end":140460282,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs558408686","clinical_significance":[]},{"source":"dbSNP","start":140460283,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140460283,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585470360"},{"seq_region_name":"7","id":"rs1585470367","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460284,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140460284},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460285,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140460285,"seq_region_name":"7","id":"rs2130269696","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130269722","clinical_significance":[],"alleles":["A","T"],"end":140460286,"strand":1,"feature_type":"variation","start":140460286,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585470382","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460287,"feature_type":"variation","strand":1,"end":140460287,"alleles":["C","A"]},{"source":"dbSNP","start":140460287,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140460288,"alleles":["CT","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs2130269771","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130269792","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460287,"feature_type":"variation","strand":1,"end":140460290,"alleles":["CTTC","-"]},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140460289,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460289,"source":"dbSNP","seq_region_name":"7","id":"rs1585470393","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585470396","end":140460290,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140460290,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140460291,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140460290,"alleles":["-","TTTTTTTT"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130269840"},{"seq_region_name":"7","id":"rs1431187881","clinical_significance":[],"end":140460291,"alleles":["A","G","T"],"strand":1,"feature_type":"variation","start":140460291,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140460291,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140460291,"alleles":["A","AAAAAAAAA"],"strand":1,"feature_type":"variation","id":"rs2130269873","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130269887","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460292,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140460292},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460294,"feature_type":"variation","strand":1,"alleles":["T","TT"],"end":140460294,"clinical_significance":[],"seq_region_name":"7","id":"rs1387956234"},{"source":"dbSNP","start":140460294,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140460294,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130269906"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140460295,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460295,"source":"dbSNP","id":"rs1794583635","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140460296,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460296,"clinical_significance":[],"id":"rs1585470409","seq_region_name":"7"},{"end":140460297,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140460297,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585470414","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794583811","source":"dbSNP","start":140460298,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140460298,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140460299,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460299,"source":"dbSNP","id":"rs1794583874","seq_region_name":"7","clinical_significance":[]},{"alleles":["TTTTT","TTTT"],"end":140460304,"feature_type":"variation","strand":1,"source":"dbSNP","start":140460300,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1167714748","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1794583982","seq_region_name":"7","end":140460301,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140460301,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1486793741","clinical_significance":[],"strand":1,"feature_type":"variation","end":140460314,"alleles":["TTTTCTTTTCTTTT","TTTTCTTTT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460301,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460303,"feature_type":"variation","strand":1,"alleles":["TTCTT","TT"],"end":140460307,"clinical_significance":[],"seq_region_name":"7","id":"rs1184601953"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794584159","alleles":["T","C"],"end":140460304,"feature_type":"variation","strand":1,"source":"dbSNP","start":140460304,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs368309942","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460305,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140460305},{"alleles":["TTTTCTTTTTTT","TTTT"],"end":140460317,"feature_type":"variation","strand":1,"source":"dbSNP","start":140460306,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1260769692"},{"seq_region_name":"7","id":"rs1794584349","clinical_significance":[],"start":140460308,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140460308,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1585470466","seq_region_name":"7","feature_type":"variation","strand":1,"end":140460311,"alleles":["TCT","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460309},{"seq_region_name":"7","id":"rs372520339","clinical_significance":[],"strand":1,"feature_type":"variation","end":140460310,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460310,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460311,"source":"dbSNP","strand":1,"feature_type":"variation","end":140460327,"alleles":["TTTTTTTTTTTTTTTTT","TTTTTTTTTTTT","TTTTTTTTTTTTT","TTTTTTTTTTTTTT","TTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTT"],"seq_region_name":"7","id":"rs57140647","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794584855","clinical_significance":[],"start":140460312,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A","C"],"end":140460312,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1794584918","seq_region_name":"7","end":140460312,"alleles":["-","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140460313,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1323917730","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460313,"feature_type":"variation","strand":1,"end":140460313,"alleles":["T","A","C"]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140460314,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460314,"clinical_significance":[],"id":"rs1428203099","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["-","C"],"end":140460314,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460315,"clinical_significance":[],"seq_region_name":"7","id":"rs932093105"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460315,"feature_type":"variation","strand":1,"end":140460315,"alleles":["T","C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1043783772"},{"alleles":["-","C"],"end":140460315,"strand":1,"feature_type":"variation","start":140460316,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794585266","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460316,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140460316,"seq_region_name":"7","id":"rs1431548564","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585470537","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460317,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140460317},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140460318,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460318,"source":"dbSNP","seq_region_name":"7","id":"rs1794585445","clinical_significance":[]},{"clinical_significance":[],"id":"rs1585470539","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["-","G"],"end":140460319,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460320},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794585554","source":"dbSNP","start":140460320,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140460320,"alleles":["T","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794585619","end":140460321,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140460321,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140460328,"alleles":["TTTG","-"],"strand":1,"feature_type":"variation","start":140460325,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794585688","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794585744","feature_type":"variation","strand":1,"end":140460326,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460326},{"start":140460326,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140460328,"alleles":["TTG","-"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1411191234","clinical_significance":[]},{"source":"dbSNP","start":140460327,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140460328,"alleles":["TG","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1468261199"},{"clinical_significance":[],"id":"rs891974386","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460328,"feature_type":"variation","strand":1,"end":140460328,"alleles":["G","C","T"]},{"start":140460328,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","-"],"end":140460328,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1307070958","clinical_significance":[]},{"source":"dbSNP","start":140460328,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140460331,"alleles":["GAGA","GA"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1458201874"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460329,"feature_type":"variation","strand":1,"end":140460329,"alleles":["A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1346360884"},{"alleles":["G","C"],"end":140460330,"feature_type":"variation","strand":1,"source":"dbSNP","start":140460330,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1794586156","seq_region_name":"7"},{"start":140460331,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C","G"],"end":140460331,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs765193838","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140460332,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460332,"clinical_significance":[],"seq_region_name":"7","id":"rs1184417582"},{"feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140460335,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460335,"clinical_significance":[],"seq_region_name":"7","id":"rs1014393075"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460337,"feature_type":"variation","strand":1,"end":140460337,"alleles":["T","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794586452"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460338,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","-"],"end":140460338,"seq_region_name":"7","id":"rs1794586499","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140460340,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460340,"source":"dbSNP","seq_region_name":"7","id":"rs1287543957","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794586619","clinical_significance":[],"alleles":["G","C"],"end":140460341,"strand":1,"feature_type":"variation","start":140460341,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs925445233","source":"dbSNP","start":140460342,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140460342,"alleles":["C","A","T"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140460343,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140460343,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1489608483"},{"clinical_significance":[],"seq_region_name":"7","id":"rs373515831","source":"dbSNP","start":140460347,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140460347,"feature_type":"variation","strand":1},{"end":140460348,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140460348,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794586879","clinical_significance":[]},{"id":"rs2130270967","seq_region_name":"7","clinical_significance":[],"end":140460349,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140460349,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1244540121","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460350,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140460350},{"clinical_significance":[],"id":"rs1405179597","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","A","G"],"end":140460351,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460351},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460354,"feature_type":"variation","strand":1,"end":140460354,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794587009"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1229665467","end":140460359,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140460359,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140460363,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460363,"source":"dbSNP","seq_region_name":"7","id":"rs1284757255","clinical_significance":[]},{"source":"dbSNP","start":140460366,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140460366,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794587191"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1348142660","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140460369,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460369},{"seq_region_name":"7","id":"rs1343120691","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140460370,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460370,"source":"dbSNP"},{"start":140460371,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140460371,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs569471009","clinical_significance":[]},{"alleles":["G","C"],"end":140460373,"feature_type":"variation","strand":1,"source":"dbSNP","start":140460373,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs182055060"},{"seq_region_name":"7","id":"rs1284308777","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140460374,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460374,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1794587522","clinical_significance":[],"end":140460378,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140460378,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1291516320","clinical_significance":[],"start":140460379,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140460379,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140460380,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140460380,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794587641"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460384,"feature_type":"variation","strand":1,"end":140460384,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1457269202"},{"seq_region_name":"7","id":"rs1389278233","clinical_significance":[],"strand":1,"feature_type":"variation","end":140460386,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460386,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460387,"source":"dbSNP","strand":1,"feature_type":"variation","end":140460387,"alleles":["G","A"],"seq_region_name":"7","id":"rs1161329968","clinical_significance":[]},{"id":"rs1471637347","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140460391,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460391,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1318728250","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460394,"feature_type":"variation","strand":1,"end":140460394,"alleles":["C","G"]},{"clinical_significance":[],"id":"rs1199684336","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460397,"feature_type":"variation","strand":1,"end":140460397,"alleles":["C","T"]},{"alleles":["C","G"],"end":140460398,"strand":1,"feature_type":"variation","start":140460398,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130271399","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140460399,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460399,"clinical_significance":[],"seq_region_name":"7","id":"rs1435072038"},{"source":"dbSNP","start":140460401,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140460401,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1265610194","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794588155","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460402,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140460402},{"end":140460404,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140460404,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1209616626","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs914513395","source":"dbSNP","start":140460405,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140460405,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1259940360","clinical_significance":[],"end":140460410,"alleles":["T","A","G"],"strand":1,"feature_type":"variation","start":140460410,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460411,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140460411,"clinical_significance":[],"seq_region_name":"7","id":"rs1207333725"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140460414,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460414,"source":"dbSNP","id":"rs1585470730","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs151213455","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460422,"feature_type":"variation","strand":1,"end":140460426,"alleles":["GCCTC","-"]},{"clinical_significance":[],"id":"rs1794588588","seq_region_name":"7","alleles":["C","T"],"end":140460424,"feature_type":"variation","strand":1,"source":"dbSNP","start":140460424,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460426,"feature_type":"variation","strand":1,"end":140460426,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585470743"},{"seq_region_name":"7","id":"rs1200456999","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["CCTCCC","C"],"end":140460434,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460429,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs555411518","source":"dbSNP","start":140460434,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140460434,"alleles":["C","T"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140460436,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460436,"clinical_significance":[],"seq_region_name":"7","id":"rs1479568328"},{"strand":1,"feature_type":"variation","end":140460437,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460437,"source":"dbSNP","id":"rs1794588960","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140460438,"alleles":["T","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460438,"source":"dbSNP","seq_region_name":"7","id":"rs1013834805","clinical_significance":[]},{"id":"rs1190729659","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460439,"source":"dbSNP","strand":1,"feature_type":"variation","end":140460439,"alleles":["A","G"]},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140460440,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460440,"clinical_significance":[],"seq_region_name":"7","id":"rs1794589077"},{"clinical_significance":[],"id":"rs1794589134","seq_region_name":"7","source":"dbSNP","start":140460443,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140460443,"alleles":["G","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794589199","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140460445,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460445},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140460447,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460447,"source":"dbSNP","seq_region_name":"7","id":"rs1794589259","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460449,"feature_type":"variation","strand":1,"end":140460449,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1385978414"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460450,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140460450,"clinical_significance":[],"seq_region_name":"7","id":"rs2130271930"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794589329","source":"dbSNP","start":140460452,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140460452,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1365720471","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140460454,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460454},{"clinical_significance":[],"seq_region_name":"7","id":"rs185416868","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460455,"feature_type":"variation","strand":1,"end":140460455,"alleles":["G","A"]},{"alleles":["C","T"],"end":140460456,"feature_type":"variation","strand":1,"source":"dbSNP","start":140460456,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794589529"},{"clinical_significance":[],"id":"rs1794589592","seq_region_name":"7","source":"dbSNP","start":140460468,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140460468,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1042812165","feature_type":"variation","strand":1,"end":140460469,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460469},{"alleles":["C","T"],"end":140460473,"feature_type":"variation","strand":1,"source":"dbSNP","start":140460473,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs905491936"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585470823","source":"dbSNP","start":140460478,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C","G"],"end":140460478,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs2130272122","clinical_significance":[],"start":140460479,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140460479,"alleles":["T","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs748453880","clinical_significance":[],"alleles":["G","C","T"],"end":140460482,"strand":1,"feature_type":"variation","start":140460482,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1467711608","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460483,"feature_type":"variation","strand":1,"end":140460483,"alleles":["T","C"]},{"clinical_significance":[],"id":"rs1376101021","seq_region_name":"7","end":140460486,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140460486,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460490,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140460490,"seq_region_name":"7","id":"rs923936556","clinical_significance":[]},{"seq_region_name":"7","id":"rs1345000986","clinical_significance":[],"end":140460492,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140460492,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460494,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140460494,"id":"rs951893769","seq_region_name":"7","clinical_significance":[]},{"end":140460495,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140460495,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1425632021"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794590247","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140460496,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460496},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794590303","alleles":["T","C"],"end":140460498,"feature_type":"variation","strand":1,"source":"dbSNP","start":140460498,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1794590354","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460500,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140460500},{"id":"rs1187070229","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140460501,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460501,"source":"dbSNP"},{"end":140460502,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140460502,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs939451820"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460506,"feature_type":"variation","strand":1,"end":140460506,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs147548013"},{"seq_region_name":"7","id":"rs895325765","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140460507,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460507,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1200528997","clinical_significance":[],"start":140460510,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140460510,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs140282837","clinical_significance":[],"start":140460511,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140460511,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794590790","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460511,"feature_type":"variation","strand":1,"alleles":["GG","G"],"end":140460512},{"end":140460513,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140460513,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs34139784"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794590953","source":"dbSNP","start":140460515,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140460515,"alleles":["G","A","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1279685237","source":"dbSNP","start":140460520,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140460520,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs556348069","seq_region_name":"7","alleles":["G","A","C"],"end":140460521,"feature_type":"variation","strand":1,"source":"dbSNP","start":140460521,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["A","T"],"end":140460523,"feature_type":"variation","strand":1,"source":"dbSNP","start":140460523,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1942569539"},{"seq_region_name":"7","id":"rs1794591172","clinical_significance":[],"start":140460530,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C","G"],"end":140460530,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140460531,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460531,"source":"dbSNP","seq_region_name":"7","id":"rs1585470924","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794591311","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460532,"source":"dbSNP","strand":1,"feature_type":"variation","end":140460532,"alleles":["C","G"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460539,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140460539,"id":"rs1794591376","seq_region_name":"7","clinical_significance":[]},{"start":140460546,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140460546,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1299477192","clinical_significance":[]},{"seq_region_name":"7","id":"rs1222012458","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460550,"source":"dbSNP","strand":1,"feature_type":"variation","end":140460550,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1794591541","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460557,"source":"dbSNP","strand":1,"feature_type":"variation","end":140460557,"alleles":["T","A"]},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140460561,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460561,"clinical_significance":[],"seq_region_name":"7","id":"rs2130272527"},{"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140460564,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460564,"source":"dbSNP","id":"rs1364371543","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460569,"source":"dbSNP","strand":1,"feature_type":"variation","end":140460572,"alleles":["GGGG","GGGGGG"],"seq_region_name":"7","id":"rs544747483","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140460570,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460570,"source":"dbSNP","seq_region_name":"7","id":"rs1397837020","clinical_significance":[]},{"start":140460572,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140460572,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794591820","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794591869","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460575,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140460575},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460578,"source":"dbSNP","strand":1,"feature_type":"variation","end":140460578,"alleles":["G","A"],"seq_region_name":"7","id":"rs1005103827","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460580,"source":"dbSNP","strand":1,"feature_type":"variation","end":140460580,"alleles":["T","C","G"],"seq_region_name":"7","id":"rs545678938","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794592078","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140460581,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460581},{"id":"rs1794592148","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140460582,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460582,"source":"dbSNP"},{"seq_region_name":"7","id":"rs965701222","clinical_significance":[],"alleles":["G","A","C"],"end":140460585,"strand":1,"feature_type":"variation","start":140460585,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140460587,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460587,"clinical_significance":[],"id":"rs997227655","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1794592340","seq_region_name":"7","source":"dbSNP","start":140460588,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140460588,"alleles":["A","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1794592396","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460590,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140460590},{"feature_type":"variation","strand":1,"end":140460592,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460592,"clinical_significance":[],"seq_region_name":"7","id":"rs1028732547"},{"clinical_significance":[],"seq_region_name":"7","id":"rs567805095","end":140460593,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140460593,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1190277296","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460596,"source":"dbSNP","strand":1,"feature_type":"variation","end":140460596,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs925386581","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460597,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140460597},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140460598,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460598,"source":"dbSNP","seq_region_name":"7","id":"rs557704067","clinical_significance":[]},{"clinical_significance":[],"id":"rs1794592822","seq_region_name":"7","end":140460602,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140460602,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","T"],"end":140460608,"feature_type":"variation","strand":1,"source":"dbSNP","start":140460608,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs989965405"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140460613,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460613,"source":"dbSNP","seq_region_name":"7","id":"rs1794592939","clinical_significance":[]},{"alleles":["C","T"],"end":140460615,"strand":1,"feature_type":"variation","start":140460615,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130272861","clinical_significance":[]},{"id":"rs1342421210","seq_region_name":"7","clinical_significance":[],"end":140460617,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140460617,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460625,"feature_type":"variation","strand":1,"end":140460625,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794593048"},{"start":140460634,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140460634,"strand":1,"feature_type":"variation","id":"rs1794593102","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140460637,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460637,"clinical_significance":[],"seq_region_name":"7","id":"rs1489940854"},{"alleles":["A","C","G"],"end":140460642,"feature_type":"variation","strand":1,"source":"dbSNP","start":140460642,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1276420755"},{"id":"rs1794593339","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140460647,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460647,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1794593395","clinical_significance":[],"end":140460650,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140460650,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs781492428","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460651,"source":"dbSNP","strand":1,"feature_type":"variation","end":140460651,"alleles":["T","C"]},{"end":140460655,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140460655,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1284589831","clinical_significance":[]},{"seq_region_name":"7","id":"rs1052643210","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140460656,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460656,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1794593625","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460658,"source":"dbSNP","strand":1,"feature_type":"variation","end":140460658,"alleles":["G","T"]},{"id":"rs1338633701","seq_region_name":"7","clinical_significance":[],"start":140460664,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140460664,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1794593750","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460667,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140460667},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140460668,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460668,"clinical_significance":[],"id":"rs918083964","seq_region_name":"7"},{"seq_region_name":"7","id":"rs575880680","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460669,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140460669},{"seq_region_name":"7","id":"rs1410576621","clinical_significance":[],"start":140460675,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140460675,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs949674049","source":"dbSNP","start":140460683,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140460683,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460686,"feature_type":"variation","strand":1,"end":140460686,"alleles":["A","G","T"],"clinical_significance":[],"id":"rs1306448107","seq_region_name":"7"},{"start":140460687,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140460692,"alleles":["TATTTA","TA"],"strand":1,"feature_type":"variation","id":"rs763850499","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1429482523","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140460693,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460693},{"strand":1,"feature_type":"variation","end":140460696,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460696,"source":"dbSNP","seq_region_name":"7","id":"rs1045279327","clinical_significance":[]},{"seq_region_name":"7","id":"rs75795158","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460697,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140460697},{"alleles":["A","-"],"end":140460701,"feature_type":"variation","strand":1,"source":"dbSNP","start":140460701,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1481633494"},{"clinical_significance":[],"seq_region_name":"7","id":"rs905543449","source":"dbSNP","start":140460706,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140460706,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1186604508","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460707,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140460707},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794594581","source":"dbSNP","start":140460710,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140460710,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs543273586","clinical_significance":[],"strand":1,"feature_type":"variation","end":140460711,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460711,"source":"dbSNP"},{"seq_region_name":"7","id":"rs571623856","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460715,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140460715},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460716,"source":"dbSNP","strand":1,"feature_type":"variation","end":140460716,"alleles":["A","G"],"seq_region_name":"7","id":"rs1048700244","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460718,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140460718,"seq_region_name":"7","id":"rs1794594859","clinical_significance":[]},{"id":"rs1202529690","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140460722,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460722,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1436896760","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140460726,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460726},{"source":"dbSNP","start":140460728,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140460728,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1794595050","seq_region_name":"7"},{"end":140460734,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140460734,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794595112","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140460735,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460735,"source":"dbSNP","seq_region_name":"7","id":"rs1290245148","clinical_significance":[]},{"alleles":["T","A"],"end":140460738,"strand":1,"feature_type":"variation","start":140460738,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585471205","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140460740,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460740,"clinical_significance":[],"id":"rs1794595297","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460744,"feature_type":"variation","strand":1,"end":140460744,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794595351"},{"start":140460751,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140460751,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794595403","clinical_significance":[]},{"seq_region_name":"7","id":"rs1445733648","clinical_significance":[],"alleles":["G","C"],"end":140460752,"strand":1,"feature_type":"variation","start":140460752,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140460756,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140460756,"alleles":["T","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs887554008"},{"source":"dbSNP","start":140460760,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140460760,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs746392284","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460761,"source":"dbSNP","strand":1,"feature_type":"variation","end":140460761,"alleles":["T","A"],"id":"rs2130273391","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140460765,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140460765,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794595710"},{"clinical_significance":[],"id":"rs190665036","seq_region_name":"7","source":"dbSNP","start":140460766,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140460766,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs923954728","clinical_significance":[],"alleles":["T","C"],"end":140460767,"strand":1,"feature_type":"variation","start":140460767,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140460770,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460770,"source":"dbSNP","seq_region_name":"7","id":"rs1286552256","clinical_significance":[]},{"id":"rs1441694133","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140460772,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460772,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140460776,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460776,"source":"dbSNP","seq_region_name":"7","id":"rs1794596025","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140460778,"alleles":["T","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460778,"clinical_significance":[],"seq_region_name":"7","id":"rs1794596095"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563089370","source":"dbSNP","start":140460779,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140460779,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs772019203","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460781,"feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140460781},{"id":"rs1014747498","seq_region_name":"7","clinical_significance":[],"alleles":["G","C"],"end":140460782,"strand":1,"feature_type":"variation","start":140460782,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140460785,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140460785,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1329037653","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1794596441","seq_region_name":"7","alleles":["T","C"],"end":140460790,"feature_type":"variation","strand":1,"source":"dbSNP","start":140460790,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460793,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140460793,"seq_region_name":"7","id":"rs180679332","clinical_significance":[]},{"source":"dbSNP","start":140460795,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AAA","AA"],"end":140460797,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1404021699","seq_region_name":"7"},{"source":"dbSNP","start":140460797,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140460797,"alleles":["A","C","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs997846576"},{"start":140460804,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140460804,"alleles":["A","T"],"strand":1,"feature_type":"variation","id":"rs939303615","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794596741","clinical_significance":[],"alleles":["G","C"],"end":140460805,"strand":1,"feature_type":"variation","start":140460805,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1473870973","clinical_significance":[],"strand":1,"feature_type":"variation","end":140460809,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460809,"source":"dbSNP"},{"id":"rs550311379","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460810,"source":"dbSNP","strand":1,"feature_type":"variation","end":140460810,"alleles":["T","C"]},{"source":"dbSNP","start":140460812,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","TT"],"end":140460812,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1297087349"},{"feature_type":"variation","strand":1,"end":140460814,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460814,"clinical_significance":[],"id":"rs916688019","seq_region_name":"7"},{"end":140460815,"alleles":["G","C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140460815,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs953517448"},{"source":"dbSNP","start":140460817,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["CATACA","CA"],"end":140460822,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1246981725"},{"source":"dbSNP","start":140460820,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140460820,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1563089397","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1794597244","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460826,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140460826},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460828,"source":"dbSNP","strand":1,"feature_type":"variation","end":140460828,"alleles":["C","T"],"id":"rs1223487391","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","G"],"end":140460829,"feature_type":"variation","strand":1,"source":"dbSNP","start":140460829,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1794597348","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140460830,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460830,"source":"dbSNP","seq_region_name":"7","id":"rs1449694368","clinical_significance":[]},{"alleles":["A","T"],"end":140460834,"strand":1,"feature_type":"variation","start":140460834,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130273783","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140460835,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460835,"clinical_significance":[],"seq_region_name":"7","id":"rs1585471388"},{"seq_region_name":"7","id":"rs1794597527","clinical_significance":[],"start":140460841,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140460841,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460842,"source":"dbSNP","strand":1,"feature_type":"variation","end":140460842,"alleles":["G","A","C"],"seq_region_name":"7","id":"rs979450672","clinical_significance":[]},{"source":"dbSNP","start":140460843,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140460843,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1248078969"},{"feature_type":"variation","strand":1,"end":140460849,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460849,"clinical_significance":[],"seq_region_name":"7","id":"rs185251114"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794597795","end":140460853,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140460853,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140460857,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460857,"clinical_significance":[],"seq_region_name":"7","id":"rs1331176828"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1358376306","end":140460858,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140460858,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794598354","source":"dbSNP","start":140460859,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140460859,"feature_type":"variation","strand":1},{"end":140460860,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140460860,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1227990061"},{"seq_region_name":"7","id":"rs190067339","clinical_significance":[],"strand":1,"feature_type":"variation","end":140460861,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460861,"source":"dbSNP"},{"start":140460862,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140460862,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794598521","clinical_significance":[]},{"seq_region_name":"7","id":"rs988189560","clinical_significance":[],"start":140460863,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140460863,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1439750865","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460865,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140460865},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794598749","feature_type":"variation","strand":1,"alleles":["G","-"],"end":140460865,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460865},{"id":"rs1794598815","seq_region_name":"7","clinical_significance":[],"alleles":["C","A"],"end":140460866,"strand":1,"feature_type":"variation","start":140460866,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1794598874","clinical_significance":[],"start":140460872,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140460872,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1276872316","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460882,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140460882},{"feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140460885,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460885,"clinical_significance":[],"id":"rs760354763","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2885922","feature_type":"variation","strand":1,"end":140460887,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460887},{"source":"dbSNP","start":140460893,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140460893,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1459226683"},{"seq_region_name":"7","id":"rs1387109522","clinical_significance":[],"start":140460894,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140460894,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1237635027","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460897,"feature_type":"variation","strand":1,"end":140460897,"alleles":["T","C"]},{"alleles":["G","A"],"end":140460898,"strand":1,"feature_type":"variation","start":140460898,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs981441517","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140460900,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460900,"clinical_significance":[],"seq_region_name":"7","id":"rs1794599394"},{"seq_region_name":"7","id":"rs1425390953","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140460903,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460903,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794599526","feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140460904,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460904},{"alleles":["T","C"],"end":140460907,"strand":1,"feature_type":"variation","start":140460907,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1192613504","clinical_significance":[]},{"id":"rs1462199835","seq_region_name":"7","clinical_significance":[],"end":140460909,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140460909,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs56898551","source":"dbSNP","start":140460910,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140460910,"alleles":["C","T"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140460911,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140460911,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs931548603"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794599866","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140460914,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460914},{"clinical_significance":[],"id":"rs1005565844","seq_region_name":"7","end":140460915,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140460915,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1466151961","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460919,"feature_type":"variation","strand":1,"end":140460919,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs530595001","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460920,"feature_type":"variation","strand":1,"end":140460920,"alleles":["T","A","C"]},{"start":140460921,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140460921,"alleles":["G","A","C","T"],"strand":1,"feature_type":"variation","id":"rs776132740","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130274312","source":"dbSNP","start":140460923,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140460923,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1794600319","clinical_significance":[],"strand":1,"feature_type":"variation","end":140460927,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460927,"source":"dbSNP"},{"alleles":["G","A"],"end":140460928,"strand":1,"feature_type":"variation","start":140460928,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1217653621","clinical_significance":[]},{"clinical_significance":[],"id":"rs1421271003","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140460930,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460930},{"seq_region_name":"7","id":"rs902080384","clinical_significance":[],"start":140460933,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140460933,"alleles":["C","A","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs997162854","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140460934,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460934,"source":"dbSNP"},{"alleles":["T","C"],"end":140460938,"feature_type":"variation","strand":1,"source":"dbSNP","start":140460938,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794600649"},{"end":140460940,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140460940,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794600713"},{"end":140460941,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140460941,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794600771"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794600825","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460943,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140460943},{"source":"dbSNP","start":140460946,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140460946,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs76357496"},{"clinical_significance":[],"id":"rs1794600996","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","-"],"end":140460955,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460955},{"seq_region_name":"7","id":"rs1406159994","clinical_significance":[],"alleles":["T","C"],"end":140460957,"strand":1,"feature_type":"variation","start":140460957,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460959,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140460959,"seq_region_name":"7","id":"rs901692566","clinical_significance":[]},{"seq_region_name":"7","id":"rs953165598","clinical_significance":[],"end":140460960,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140460960,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140460964,"alleles":["A","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460964,"source":"dbSNP","id":"rs1794601267","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1011246722","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140460965,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460965},{"source":"dbSNP","start":140460967,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140460967,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1021878862"},{"alleles":["G","A"],"end":140460973,"strand":1,"feature_type":"variation","start":140460973,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1585471717","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1394113921","seq_region_name":"7","source":"dbSNP","start":140460974,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140460974,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1794601544","clinical_significance":[],"alleles":["C","A","T"],"end":140460982,"strand":1,"feature_type":"variation","start":140460982,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794601626","source":"dbSNP","start":140460983,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140460983,"alleles":["A","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1794601695","clinical_significance":[],"alleles":["C","T"],"end":140460984,"strand":1,"feature_type":"variation","start":140460984,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794601765","end":140460985,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140460985,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460991,"feature_type":"variation","strand":1,"end":140460991,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794601829"},{"clinical_significance":[],"id":"rs1168974541","seq_region_name":"7","source":"dbSNP","start":140460995,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140460995,"alleles":["A","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs967212341","feature_type":"variation","strand":1,"alleles":["A","T"],"end":140460997,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140460997},{"id":"rs1259549496","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140460999,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140460999},{"seq_region_name":"7","id":"rs977753688","clinical_significance":[],"start":140461005,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140461005,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794602104","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461006,"feature_type":"variation","strand":1,"end":140461006,"alleles":["T","G"]},{"source":"dbSNP","start":140461007,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140461007,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1000775671","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794602228","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461008,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140461008},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794602276","source":"dbSNP","start":140461013,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140461013,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1381793094","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140461015,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461015,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140461018,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461018,"clinical_significance":[],"id":"rs1794602389","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1032351273","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461020,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140461020},{"seq_region_name":"7","id":"rs567737679","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461021,"source":"dbSNP","strand":1,"feature_type":"variation","end":140461021,"alleles":["G","A","C"]},{"start":140461024,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140461024,"alleles":["A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794602566","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140461025,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461025,"clinical_significance":[],"seq_region_name":"7","id":"rs1485461608"},{"start":140461026,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140461026,"strand":1,"feature_type":"variation","id":"rs1794602699","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794602768","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461029,"feature_type":"variation","strand":1,"alleles":["ACA","A"],"end":140461031},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794602837","end":140461030,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140461030,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["TATA","TA"],"end":140461038,"feature_type":"variation","strand":1,"source":"dbSNP","start":140461035,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794602909"},{"source":"dbSNP","start":140461036,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140461036,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794602972"},{"seq_region_name":"7","id":"rs1431261335","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461037,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140461037},{"clinical_significance":[],"seq_region_name":"7","id":"rs768248846","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461045,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140461045},{"id":"rs928596787","seq_region_name":"7","clinical_significance":[],"alleles":["T","A","C"],"end":140461046,"strand":1,"feature_type":"variation","start":140461046,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794603232","source":"dbSNP","start":140461049,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140461049,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1794603285","clinical_significance":[],"end":140461049,"alleles":["T","TTGTT"],"strand":1,"feature_type":"variation","start":140461049,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1794603344","clinical_significance":[],"strand":1,"feature_type":"variation","end":140461051,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461051,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461054,"feature_type":"variation","strand":1,"end":140461054,"alleles":["C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794603399"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140461055,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461055,"source":"dbSNP","seq_region_name":"7","id":"rs2130274981","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794603456","end":140461056,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140461056,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1794603502","seq_region_name":"7","clinical_significance":[],"alleles":["G","T"],"end":140461060,"strand":1,"feature_type":"variation","start":140461060,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461068,"feature_type":"variation","strand":1,"end":140461068,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1231028130"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1271681488","alleles":["C","G"],"end":140461069,"feature_type":"variation","strand":1,"source":"dbSNP","start":140461069,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1340540428","alleles":["G","C"],"end":140461071,"feature_type":"variation","strand":1,"source":"dbSNP","start":140461071,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1794603681","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461073,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140461073},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461075,"source":"dbSNP","strand":1,"feature_type":"variation","end":140461075,"alleles":["A","C"],"id":"rs1341813955","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140461077,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140461085,"alleles":["ACTGACTGA","ACTGA"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1295331569"},{"id":"rs1794603853","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461083,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140461083},{"start":140461100,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140461100,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794603913","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1229352340","end":140461101,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140461101,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461105,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140461105,"clinical_significance":[],"id":"rs1794604058","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140461106,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461106,"source":"dbSNP","seq_region_name":"7","id":"rs988240229","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130275159","clinical_significance":[],"end":140461108,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140461108,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140461109,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140461109,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1304018913","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1213011294","end":140461111,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140461111,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461114,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140461114,"seq_region_name":"7","id":"rs6966049","clinical_significance":[]},{"seq_region_name":"7","id":"rs76740656","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461119,"source":"dbSNP","strand":1,"feature_type":"variation","end":140461119,"alleles":["A","C"]},{"id":"rs1206159128","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140461122,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461122,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140461123,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461123,"source":"dbSNP","id":"rs2130275247","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","A","C"],"end":140461124,"feature_type":"variation","strand":1,"source":"dbSNP","start":140461124,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs747933712"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130275271","feature_type":"variation","strand":1,"end":140461125,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461125},{"end":140461126,"alleles":["T","A","G"],"strand":1,"feature_type":"variation","start":140461126,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs6966056","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461128,"feature_type":"variation","strand":1,"end":140461128,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130275315"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130275332","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140461132,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461132},{"clinical_significance":[],"id":"rs1442328443","seq_region_name":"7","feature_type":"variation","strand":1,"end":140461134,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461134},{"strand":1,"feature_type":"variation","end":140461142,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461142,"source":"dbSNP","seq_region_name":"7","id":"rs763509963","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794605049","clinical_significance":[],"start":140461143,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140461143,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"start":140461144,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140461144,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794605109","clinical_significance":[]},{"source":"dbSNP","start":140461146,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140461146,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1185895508"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461150,"source":"dbSNP","strand":1,"feature_type":"variation","end":140461152,"alleles":["ATA","A"],"id":"rs1794605232","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794605296","source":"dbSNP","start":140461154,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140461154,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs931602475","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140461163,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461163},{"seq_region_name":"7","id":"rs1252780713","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140461164,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461164,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140461165,"alleles":["CT","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461164,"clinical_significance":[],"id":"rs1194398182","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130275465","alleles":["T","C"],"end":140461165,"feature_type":"variation","strand":1,"source":"dbSNP","start":140461165,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1794605519","clinical_significance":[],"start":140461170,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140461170,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs984306282","clinical_significance":[],"start":140461172,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140461172,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs984870489","clinical_significance":[],"alleles":["G","A"],"end":140461174,"strand":1,"feature_type":"variation","start":140461174,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1794605707","seq_region_name":"7","clinical_significance":[],"alleles":["A","C"],"end":140461176,"strand":1,"feature_type":"variation","start":140461176,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1794605769","seq_region_name":"7","clinical_significance":[],"end":140461177,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140461177,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1482212737","end":140461179,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140461179,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1794605880","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461180,"feature_type":"variation","strand":1,"alleles":["ACA","A"],"end":140461182},{"seq_region_name":"7","id":"rs767028711","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140461183,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461183,"source":"dbSNP"},{"clinical_significance":[],"id":"rs909385104","seq_region_name":"7","feature_type":"variation","strand":1,"end":140461188,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461188},{"seq_region_name":"7","id":"rs1222788793","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140461190,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461190,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140461192,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461192,"source":"dbSNP","seq_region_name":"7","id":"rs1794606064","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461194,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140461194,"seq_region_name":"7","id":"rs1324015450","clinical_significance":[]},{"id":"rs539059871","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461202,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140461202},{"seq_region_name":"7","id":"rs1794606263","clinical_significance":[],"alleles":["T","C"],"end":140461204,"strand":1,"feature_type":"variation","start":140461204,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140461205,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140461205,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs908885824","clinical_significance":[]},{"clinical_significance":[],"id":"rs1230902749","seq_region_name":"7","alleles":["A","C"],"end":140461209,"feature_type":"variation","strand":1,"source":"dbSNP","start":140461209,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["T","C"],"end":140461219,"strand":1,"feature_type":"variation","start":140461219,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794606459","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs752155615","end":140461222,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140461222,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1794606592","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140461227,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461227,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794606642","source":"dbSNP","start":140461231,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140461231,"alleles":["T","G"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461234,"feature_type":"variation","strand":1,"end":140461234,"alleles":["A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794606697"},{"clinical_significance":[],"id":"rs1474257293","seq_region_name":"7","feature_type":"variation","strand":1,"end":140461239,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461239},{"seq_region_name":"7","id":"rs1794606839","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461243,"source":"dbSNP","strand":1,"feature_type":"variation","end":140461243,"alleles":["T","G"]},{"strand":1,"feature_type":"variation","end":140461258,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461258,"source":"dbSNP","seq_region_name":"7","id":"rs1288464085","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130275835","clinical_significance":[],"strand":1,"feature_type":"variation","end":140461260,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461260,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461261,"feature_type":"variation","strand":1,"end":140461261,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794606950"},{"id":"rs1794607005","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140461262,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461262,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs940337392","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461264,"feature_type":"variation","strand":1,"end":140461264,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1393900459","source":"dbSNP","start":140461265,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140461265,"alleles":["T","-"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130275907","end":140461265,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140461265,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1794607188","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140461271,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461271,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1036535292","source":"dbSNP","start":140461272,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140461272,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461280,"source":"dbSNP","strand":1,"feature_type":"variation","end":140461280,"alleles":["T","C"],"seq_region_name":"7","id":"rs1192412633","clinical_significance":[]},{"seq_region_name":"7","id":"rs1429414077","clinical_significance":[],"end":140461282,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140461282,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461287,"source":"dbSNP","strand":1,"feature_type":"variation","end":140461287,"alleles":["T","C"],"seq_region_name":"7","id":"rs1794607444","clinical_significance":[]},{"seq_region_name":"7","id":"rs1470641224","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461290,"source":"dbSNP","strand":1,"feature_type":"variation","end":140461290,"alleles":["A","G"]},{"source":"dbSNP","start":140461299,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140461299,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794607633"},{"id":"rs1351518690","seq_region_name":"7","clinical_significance":[],"alleles":["C","A","T"],"end":140461306,"strand":1,"feature_type":"variation","start":140461306,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1458283092","source":"dbSNP","start":140461306,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140461314,"alleles":["CCATCTCCA","CCATCTCCATCTCCA"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461309,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140461309,"id":"rs1162763307","seq_region_name":"7","clinical_significance":[]},{"start":140461310,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140461310,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs901623434","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461319,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140461319,"clinical_significance":[],"seq_region_name":"7","id":"rs933061607"},{"strand":1,"feature_type":"variation","end":140461320,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461320,"source":"dbSNP","seq_region_name":"7","id":"rs1036919507","clinical_significance":[]},{"start":140461321,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140461321,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794608372","clinical_significance":[]},{"alleles":["GGGG","GGGGG"],"end":140461325,"strand":1,"feature_type":"variation","start":140461322,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs558596730","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461325,"source":"dbSNP","strand":1,"feature_type":"variation","end":140461325,"alleles":["G","A"],"seq_region_name":"7","id":"rs1250148271","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130276095","feature_type":"variation","strand":1,"alleles":["T","A"],"end":140461330,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461330},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461332,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140461332,"seq_region_name":"7","id":"rs1794608647","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794608720","clinical_significance":[],"start":140461335,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140461335,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs902142998","clinical_significance":[],"start":140461338,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140461338,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461341,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140461341,"clinical_significance":[],"id":"rs1401212715","seq_region_name":"7"},{"start":140461344,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140461344,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1489700852","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794609083","clinical_significance":[],"alleles":["G","A"],"end":140461348,"strand":1,"feature_type":"variation","start":140461348,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["T","A"],"end":140461353,"strand":1,"feature_type":"variation","start":140461353,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs2130276184","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461357,"source":"dbSNP","strand":1,"feature_type":"variation","end":140461357,"alleles":["T","C"],"seq_region_name":"7","id":"rs1271688700","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140461358,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461358,"clinical_significance":[],"seq_region_name":"7","id":"rs1794609253"},{"clinical_significance":[],"id":"rs1794609327","seq_region_name":"7","source":"dbSNP","start":140461359,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140461359,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1213571071","source":"dbSNP","start":140461362,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140461362,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1330433923","alleles":["C","A"],"end":140461364,"feature_type":"variation","strand":1,"source":"dbSNP","start":140461364,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140461365,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140461365,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1268147367"},{"alleles":["T","G"],"end":140461368,"strand":1,"feature_type":"variation","start":140461368,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs557666952","clinical_significance":[]},{"source":"dbSNP","start":140461370,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140461370,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1229763875"},{"id":"rs933567323","seq_region_name":"7","clinical_significance":[],"start":140461371,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140461371,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs534176511","clinical_significance":[],"alleles":["G","A"],"end":140461375,"strand":1,"feature_type":"variation","start":140461375,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140461376,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461376,"clinical_significance":[],"seq_region_name":"7","id":"rs1794610054"},{"alleles":["C","A"],"end":140461378,"feature_type":"variation","strand":1,"source":"dbSNP","start":140461378,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794610123"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461380,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140461380,"id":"rs1794610225","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140461391,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140461395,"alleles":["CCAAC","CCAACCAAC"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1387112350","seq_region_name":"7"},{"alleles":["C","T"],"end":140461392,"strand":1,"feature_type":"variation","start":140461392,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1369398913","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","C"],"end":140461399,"strand":1,"feature_type":"variation","start":140461399,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs576042204","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1460792874","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140461401,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461401},{"strand":1,"feature_type":"variation","end":140461402,"alleles":["GG","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461401,"source":"dbSNP","id":"rs1794610620","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs888742091","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461411,"source":"dbSNP","strand":1,"feature_type":"variation","end":140461411,"alleles":["G","A"]},{"source":"dbSNP","start":140461412,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140461412,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs181306331"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140461417,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461417,"clinical_significance":[],"seq_region_name":"7","id":"rs1161444045"},{"source":"dbSNP","start":140461421,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140461421,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794610831"},{"seq_region_name":"7","id":"rs1794610877","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","-"],"end":140461421,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461421,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["TT","-"],"end":140461426,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461425,"source":"dbSNP","id":"rs2130276512","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461427,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140461427,"clinical_significance":[],"seq_region_name":"7","id":"rs2130276527"},{"strand":1,"feature_type":"variation","alleles":["A","C","G","T"],"end":140461428,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461428,"source":"dbSNP","seq_region_name":"7","id":"rs1021344579","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794611121","clinical_significance":[],"alleles":["G","A"],"end":140461429,"strand":1,"feature_type":"variation","start":140461429,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130276567","source":"dbSNP","start":140461431,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140461431,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1363406141","alleles":["G","C"],"end":140461434,"feature_type":"variation","strand":1,"source":"dbSNP","start":140461434,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130276599","end":140461440,"alleles":["TGT","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140461438,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140461439,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140461439,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794611275"},{"seq_region_name":"7","id":"rs970877766","clinical_significance":[],"strand":1,"feature_type":"variation","end":140461444,"alleles":["AAGA","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461441,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130276641","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461442,"feature_type":"variation","strand":1,"alleles":["-","TCG"],"end":140461441},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140461442,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461442,"clinical_significance":[],"seq_region_name":"7","id":"rs554912627"},{"id":"rs1251452349","seq_region_name":"7","clinical_significance":[],"end":140461443,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140461443,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140461445,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461445,"clinical_significance":[],"seq_region_name":"7","id":"rs902917315"},{"seq_region_name":"7","id":"rs2130276704","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461448,"source":"dbSNP","strand":1,"feature_type":"variation","end":140461448,"alleles":["G","T"]},{"end":140461453,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140461453,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1193420581"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461454,"source":"dbSNP","strand":1,"feature_type":"variation","end":140461454,"alleles":["C","T"],"seq_region_name":"7","id":"rs752859458","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130276748","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461455,"feature_type":"variation","strand":1,"alleles":["-","TGACATGGT"],"end":140461454},{"seq_region_name":"7","id":"rs1794611884","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140461455,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461455,"source":"dbSNP"},{"source":"dbSNP","start":140461458,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140461458,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1794611929","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140461459,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461459,"source":"dbSNP","seq_region_name":"7","id":"rs1794611997","clinical_significance":[]},{"source":"dbSNP","start":140461461,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140461461,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130276793"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461462,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140461462,"seq_region_name":"7","id":"rs998721089","clinical_significance":[]},{"seq_region_name":"7","id":"rs1206231171","clinical_significance":[],"start":140461463,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140461463,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140461465,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140461465,"alleles":["C","A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1002693426"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461468,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140461468,"clinical_significance":[],"seq_region_name":"7","id":"rs1445596276"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461470,"source":"dbSNP","strand":1,"feature_type":"variation","end":140461470,"alleles":["C","T"],"seq_region_name":"7","id":"rs1585472274","clinical_significance":[]},{"seq_region_name":"7","id":"rs1033862213","clinical_significance":[],"end":140461472,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140461472,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140461477,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461477,"clinical_significance":[],"id":"rs1794612540","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140461480,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461480,"clinical_significance":[],"seq_region_name":"7","id":"rs1794612657"},{"start":140461482,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140461482,"alleles":["A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794612755","clinical_significance":[]},{"id":"rs1585472283","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461483,"source":"dbSNP","strand":1,"feature_type":"variation","end":140461483,"alleles":["A","G"]},{"source":"dbSNP","start":140461485,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140461485,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1794612928","seq_region_name":"7"},{"alleles":["C","T"],"end":140461488,"feature_type":"variation","strand":1,"source":"dbSNP","start":140461488,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1794613021","seq_region_name":"7"},{"seq_region_name":"7","id":"rs756365193","clinical_significance":[],"end":140461489,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140461489,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140461490,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140461490,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs573387518"},{"alleles":["C","T"],"end":140461493,"strand":1,"feature_type":"variation","start":140461493,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794613289","clinical_significance":[]},{"alleles":["T","C"],"end":140461495,"feature_type":"variation","strand":1,"source":"dbSNP","start":140461495,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1300906238"},{"end":140461497,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140461497,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1439971328"},{"alleles":["C","T"],"end":140461501,"feature_type":"variation","strand":1,"source":"dbSNP","start":140461501,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs991367312"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140461502,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461502,"source":"dbSNP","seq_region_name":"7","id":"rs540729256","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461503,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140461503,"clinical_significance":[],"seq_region_name":"7","id":"rs559413970"},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140461505,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461505,"source":"dbSNP","seq_region_name":"7","id":"rs577537641","clinical_significance":[]},{"clinical_significance":[],"id":"rs1794614127","seq_region_name":"7","feature_type":"variation","strand":1,"end":140461507,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461507},{"id":"rs1173239642","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140461508,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461508,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140461510,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461510,"clinical_significance":[],"id":"rs1467723618","seq_region_name":"7"},{"start":140461515,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140461515,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1470478310","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461520,"feature_type":"variation","strand":1,"end":140461520,"alleles":["C","G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1173405081"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140461526,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461526,"source":"dbSNP","seq_region_name":"7","id":"rs1563089670","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794614668","source":"dbSNP","start":140461530,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140461530,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1794614747","clinical_significance":[],"start":140461532,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140461532,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461533,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140461533,"seq_region_name":"7","id":"rs1794614813","clinical_significance":[]},{"clinical_significance":[],"id":"rs1450528079","seq_region_name":"7","source":"dbSNP","start":140461534,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140461534,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1392547289","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461539,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140461539},{"id":"rs1160159009","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140461541,"alleles":["A","C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461541,"source":"dbSNP"},{"seq_region_name":"7","id":"rs186654084","clinical_significance":[],"start":140461543,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140461543,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs757367027","end":140461548,"alleles":["T","A","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140461548,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1260347980","feature_type":"variation","strand":1,"end":140461551,"alleles":["T","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461551},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140461555,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461555,"source":"dbSNP","seq_region_name":"7","id":"rs191443949","clinical_significance":[]},{"alleles":["C","G"],"end":140461557,"strand":1,"feature_type":"variation","start":140461557,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1486440871","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794615663","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461558,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140461558},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794615753","source":"dbSNP","start":140461560,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140461560,"alleles":["G","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1277831437","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461562,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140461562},{"source":"dbSNP","start":140461564,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140461564,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1233251900"},{"strand":1,"feature_type":"variation","end":140461565,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461565,"source":"dbSNP","seq_region_name":"7","id":"rs1342669101","clinical_significance":[]},{"clinical_significance":[],"id":"rs1585472410","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461566,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140461566},{"start":140461567,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140461567,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs530751585","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794616386","end":140461568,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140461568,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs922921082","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461570,"feature_type":"variation","strand":1,"end":140461570,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs933091240","feature_type":"variation","strand":1,"end":140461573,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461573},{"seq_region_name":"7","id":"rs1327315433","clinical_significance":[],"strand":1,"feature_type":"variation","end":140461577,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461577,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794616813","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461579,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140461579},{"seq_region_name":"7","id":"rs1325799889","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140461584,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461584,"source":"dbSNP"},{"start":140461586,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140461586,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794617009","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1050557257","feature_type":"variation","strand":1,"end":140461588,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461588},{"clinical_significance":[],"id":"rs1794617212","seq_region_name":"7","source":"dbSNP","start":140461589,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140461589,"alleles":["C","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794617292","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461591,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140461591},{"clinical_significance":[],"seq_region_name":"7","id":"rs1397932659","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461594,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140461594},{"clinical_significance":[],"seq_region_name":"7","id":"rs1366472504","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461595,"feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140461595},{"source":"dbSNP","start":140461596,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140461596,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs972292108","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1312554269","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140461597,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461597},{"clinical_significance":[],"seq_region_name":"7","id":"rs910405143","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140461598,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461598},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461602,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140461602,"seq_region_name":"7","id":"rs1372752419","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1166519747","alleles":["C","T"],"end":140461604,"feature_type":"variation","strand":1,"source":"dbSNP","start":140461604,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs923407794","source":"dbSNP","start":140461606,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140461606,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140461607,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140461607,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1475338119"},{"seq_region_name":"7","id":"rs1585472524","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140461611,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461611,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461612,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140461612,"clinical_significance":[],"seq_region_name":"7","id":"rs1585472536"},{"seq_region_name":"7","id":"rs2130277709","clinical_significance":[],"end":140461616,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140461616,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140461617,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461617,"clinical_significance":[],"seq_region_name":"7","id":"rs1369603722"},{"id":"rs1187633382","seq_region_name":"7","clinical_significance":[],"start":140461620,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140461620,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140461622,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140461622,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794619054"},{"source":"dbSNP","start":140461627,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140461627,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs936460983"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794619209","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140461628,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461628},{"feature_type":"variation","strand":1,"end":140461633,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461633,"clinical_significance":[],"seq_region_name":"7","id":"rs1794619295"},{"clinical_significance":[],"id":"rs2130277802","seq_region_name":"7","alleles":["AAAAAA","AAAAAAA"],"end":140461640,"feature_type":"variation","strand":1,"source":"dbSNP","start":140461635,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1254931036","clinical_significance":[],"end":140461639,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140461639,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1330538882","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461641,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140461641},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461644,"source":"dbSNP","strand":1,"feature_type":"variation","end":140461644,"alleles":["T","A"],"seq_region_name":"7","id":"rs1209659725","clinical_significance":[]},{"start":140461645,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140461645,"alleles":["A","T"],"strand":1,"feature_type":"variation","id":"rs374037508","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs555908205","seq_region_name":"7","end":140461653,"alleles":["AAAAAAAAA","AAAAAAAA","AAAAAAAAAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140461645,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1794619814","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140461646,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461646,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1794619875","clinical_significance":[],"start":140461647,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140461647,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1193918634","end":140461649,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140461649,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["A","C","G"],"end":140461656,"feature_type":"variation","strand":1,"source":"dbSNP","start":140461656,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794620020"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794620134","feature_type":"variation","strand":1,"end":140461671,"alleles":["AAGCATAGCAAGCAT","AAGCAT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461657},{"clinical_significance":[],"id":"rs1406986149","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461658,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140461658},{"alleles":["G","GG"],"end":140461664,"feature_type":"variation","strand":1,"source":"dbSNP","start":140461664,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs141137827"},{"seq_region_name":"7","id":"rs1585472611","clinical_significance":[],"end":140461664,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140461664,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1794620554","clinical_significance":[],"start":140461665,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140461665,"strand":1,"feature_type":"variation"},{"alleles":["A","C"],"end":140461666,"feature_type":"variation","strand":1,"source":"dbSNP","start":140461666,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1410593927"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461666,"source":"dbSNP","strand":1,"feature_type":"variation","end":140461667,"alleles":["AA","A","AAA"],"seq_region_name":"7","id":"rs906493529","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461666,"source":"dbSNP","strand":1,"feature_type":"variation","end":140461668,"alleles":["AAG","AAGAAG"],"id":"rs1046427383","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1050612940","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461668,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140461668},{"seq_region_name":"7","id":"rs1292949950","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140461674,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461674,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461676,"source":"dbSNP","strand":1,"feature_type":"variation","end":140461676,"alleles":["C","G","T"],"seq_region_name":"7","id":"rs1585472666","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140461681,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461681,"source":"dbSNP","seq_region_name":"7","id":"rs779942844","clinical_significance":[]},{"seq_region_name":"7","id":"rs947100795","clinical_significance":[],"alleles":["G","C"],"end":140461682,"strand":1,"feature_type":"variation","start":140461682,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461684,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140461684,"seq_region_name":"7","id":"rs1392041606","clinical_significance":[]},{"start":140461685,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140461684,"alleles":["-","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1490754934","clinical_significance":[]},{"alleles":["C","T"],"end":140461691,"strand":1,"feature_type":"variation","start":140461691,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs747023842","clinical_significance":[]},{"seq_region_name":"7","id":"rs1219725704","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461693,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CACA","CA"],"end":140461696},{"alleles":["C","G"],"end":140461695,"strand":1,"feature_type":"variation","start":140461695,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1794621874","seq_region_name":"7","clinical_significance":[]},{"id":"rs1414936276","seq_region_name":"7","clinical_significance":[],"end":140461696,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140461696,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140461698,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140461698,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs768328495"},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140461700,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461700,"source":"dbSNP","seq_region_name":"7","id":"rs1266058075","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1437863497","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140461701,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461701},{"alleles":["C","G"],"end":140461704,"strand":1,"feature_type":"variation","start":140461704,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1186625289","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794622324","clinical_significance":[],"start":140461705,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140461705,"alleles":["T","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1472707084","seq_region_name":"7","feature_type":"variation","strand":1,"end":140461708,"alleles":["A","AA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461708},{"feature_type":"variation","strand":1,"end":140461709,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461709,"clinical_significance":[],"seq_region_name":"7","id":"rs1043094565"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461710,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140461710,"clinical_significance":[],"seq_region_name":"7","id":"rs145472716"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461715,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140461715,"clinical_significance":[],"id":"rs1794622596","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794622688","feature_type":"variation","strand":1,"end":140461716,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461716},{"alleles":["C","G"],"end":140461723,"strand":1,"feature_type":"variation","start":140461723,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs998978999","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","C"],"end":140461725,"feature_type":"variation","strand":1,"source":"dbSNP","start":140461725,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794622895"},{"seq_region_name":"7","id":"rs1794622980","clinical_significance":[],"strand":1,"feature_type":"variation","end":140461726,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461726,"source":"dbSNP"},{"alleles":["A","T"],"end":140461728,"strand":1,"feature_type":"variation","start":140461728,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs961639034","clinical_significance":[]},{"source":"dbSNP","start":140461730,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140461730,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794623068"},{"id":"rs11974988","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140461731,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461731,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1794623279","clinical_significance":[],"start":140461735,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140461735,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1332588340","clinical_significance":[],"start":140461738,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140461738,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1272559994","clinical_significance":[],"end":140461744,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140461744,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1563089808","seq_region_name":"7","alleles":["G","C"],"end":140461748,"feature_type":"variation","strand":1,"source":"dbSNP","start":140461748,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140461749,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140461749,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585472800"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1229149081","source":"dbSNP","start":140461750,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140461750,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1794623637","clinical_significance":[],"start":140461752,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140461752,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461754,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140461754,"seq_region_name":"7","id":"rs1164047390","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140461755,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461755,"clinical_significance":[],"id":"rs773084739","seq_region_name":"7"},{"alleles":["G","A"],"end":140461756,"feature_type":"variation","strand":1,"source":"dbSNP","start":140461756,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1441906046"},{"alleles":["T","G"],"end":140461758,"strand":1,"feature_type":"variation","start":140461758,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs983508142","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461761,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140461761,"clinical_significance":[],"seq_region_name":"7","id":"rs1585472855"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794624115","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461763,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140461763},{"clinical_significance":[],"seq_region_name":"7","id":"rs1426808061","source":"dbSNP","start":140461764,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140461764,"feature_type":"variation","strand":1},{"end":140461766,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140461766,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794627193","clinical_significance":[]},{"start":140461769,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140461769,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs922963291","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461770,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140461770,"seq_region_name":"7","id":"rs1794627293","clinical_significance":[]},{"start":140461771,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140461771,"alleles":["G","T"],"strand":1,"feature_type":"variation","id":"rs560880962","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140461772,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461772,"clinical_significance":[],"seq_region_name":"7","id":"rs1585472878"},{"id":"rs1563089832","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140461773,"strand":1,"feature_type":"variation","start":140461773,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461774,"feature_type":"variation","strand":1,"end":140461774,"alleles":["G","A","C"],"clinical_significance":[],"id":"rs1022917818","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140461775,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461775,"source":"dbSNP","seq_region_name":"7","id":"rs1794627773","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs576751546","end":140461778,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140461778,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs546751155","clinical_significance":[],"start":140461781,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140461781,"strand":1,"feature_type":"variation"},{"end":140461786,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140461786,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1457351790","seq_region_name":"7"},{"alleles":["C","G"],"end":140461790,"feature_type":"variation","strand":1,"source":"dbSNP","start":140461790,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794628111"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461794,"feature_type":"variation","strand":1,"end":140461794,"alleles":["A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794628194"},{"clinical_significance":[],"seq_region_name":"7","id":"rs867252400","alleles":["C","A"],"end":140461796,"feature_type":"variation","strand":1,"source":"dbSNP","start":140461796,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1794628339","seq_region_name":"7","alleles":["T","C"],"end":140461801,"feature_type":"variation","strand":1,"source":"dbSNP","start":140461801,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1156400480","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461809,"feature_type":"variation","strand":1,"alleles":["CCCC","CC","CCCCC"],"end":140461812},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140461811,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461811,"clinical_significance":[],"seq_region_name":"7","id":"rs1794628590"},{"id":"rs1794628684","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140461812,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461812,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs984849064","end":140461813,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140461813,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140461820,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461820,"clinical_significance":[],"seq_region_name":"7","id":"rs1195278941"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461822,"source":"dbSNP","strand":1,"feature_type":"variation","end":140461822,"alleles":["A","T"],"seq_region_name":"7","id":"rs1467070906","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1016670607","alleles":["T","C"],"end":140461827,"feature_type":"variation","strand":1,"source":"dbSNP","start":140461827,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794628971","source":"dbSNP","start":140461829,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140461829,"feature_type":"variation","strand":1},{"alleles":["A","G"],"end":140461830,"strand":1,"feature_type":"variation","start":140461830,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1794629200","seq_region_name":"7","clinical_significance":[]},{"start":140461835,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140461835,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585472954","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461836,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140461836,"clinical_significance":[],"seq_region_name":"7","id":"rs374001509"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461837,"source":"dbSNP","strand":1,"feature_type":"variation","end":140461837,"alleles":["G","T"],"seq_region_name":"7","id":"rs1585472972","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs368416139","feature_type":"variation","strand":1,"end":140461839,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461839},{"clinical_significance":[],"seq_region_name":"7","id":"rs1282273576","feature_type":"variation","strand":1,"end":140461840,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461840},{"seq_region_name":"7","id":"rs1223391715","clinical_significance":[],"strand":1,"feature_type":"variation","end":140461841,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461841,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585472995","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461845,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140461845},{"clinical_significance":[],"seq_region_name":"7","id":"rs1446678688","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461846,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140461846},{"clinical_significance":[],"id":"rs923458730","seq_region_name":"7","alleles":["T","C","G"],"end":140461848,"feature_type":"variation","strand":1,"source":"dbSNP","start":140461848,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs954846475","clinical_significance":[],"start":140461851,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140461851,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140461852,"alleles":["G","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461852,"clinical_significance":[],"seq_region_name":"7","id":"rs183717864"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140461855,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461855,"clinical_significance":[],"seq_region_name":"7","id":"rs910826516"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461856,"source":"dbSNP","strand":1,"feature_type":"variation","end":140461856,"alleles":["G","A"],"seq_region_name":"7","id":"rs1794630432","clinical_significance":[]},{"id":"rs1794630490","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140461858,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461858,"source":"dbSNP"},{"alleles":["G","A"],"end":140461860,"feature_type":"variation","strand":1,"source":"dbSNP","start":140461860,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794630542"},{"start":140461865,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140461865,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs10241951","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461867,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140461867,"clinical_significance":[],"id":"rs1264446942","seq_region_name":"7"},{"id":"rs1042761386","seq_region_name":"7","clinical_significance":[],"start":140461871,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140461871,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461871,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","-"],"end":140461871,"seq_region_name":"7","id":"rs1794630811","clinical_significance":[]},{"seq_region_name":"7","id":"rs1339633836","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140461879,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461879,"source":"dbSNP"},{"clinical_significance":[],"id":"rs924235976","seq_region_name":"7","feature_type":"variation","strand":1,"end":140461880,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461880},{"strand":1,"feature_type":"variation","end":140461884,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461884,"source":"dbSNP","id":"rs769588632","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461890,"source":"dbSNP","strand":1,"feature_type":"variation","end":140461890,"alleles":["G","A"],"seq_region_name":"7","id":"rs1794631062","clinical_significance":[]},{"end":140461891,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140461891,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs371131149","clinical_significance":[]},{"start":140461893,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140461893,"alleles":["G","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs111795113","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140461894,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461894,"clinical_significance":[],"id":"rs1794631290","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794631372","source":"dbSNP","start":140461899,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140461899,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794631426","feature_type":"variation","strand":1,"end":140461901,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461901},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461902,"feature_type":"variation","strand":1,"end":140461902,"alleles":["G","C"],"clinical_significance":[],"id":"rs1794631472","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1457309485","clinical_significance":[],"start":140461907,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140461907,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs555252548","seq_region_name":"7","source":"dbSNP","start":140461913,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140461913,"alleles":["G","A"],"feature_type":"variation","strand":1},{"start":140461914,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140461914,"strand":1,"feature_type":"variation","id":"rs573322900","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs534425608","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140461915,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461915},{"clinical_significance":[],"id":"rs888404520","seq_region_name":"7","feature_type":"variation","strand":1,"end":140461919,"alleles":["G","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461919},{"clinical_significance":[],"id":"rs1585473101","seq_region_name":"7","alleles":["T","G"],"end":140461920,"feature_type":"variation","strand":1,"source":"dbSNP","start":140461920,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140461921,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140461921,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1189077481","clinical_significance":[]},{"alleles":["G","-"],"end":140461922,"strand":1,"feature_type":"variation","start":140461922,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1163776225","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140461922,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461922,"source":"dbSNP","seq_region_name":"7","id":"rs1486824698","clinical_significance":[]},{"alleles":["G","A"],"end":140461927,"strand":1,"feature_type":"variation","start":140461927,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1368151462","clinical_significance":[]},{"alleles":["C","T"],"end":140461931,"feature_type":"variation","strand":1,"source":"dbSNP","start":140461931,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585473136"},{"end":140461933,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140461933,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs766417548","clinical_significance":[]},{"source":"dbSNP","start":140461934,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140461934,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1794632237","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1794632294","clinical_significance":[],"start":140461935,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140461935,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794632361","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140461938,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461938},{"end":140461944,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140461944,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1169782701","clinical_significance":[]},{"alleles":["G","C"],"end":140461946,"strand":1,"feature_type":"variation","start":140461946,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs772812341","clinical_significance":[]},{"seq_region_name":"7","id":"rs1055038375","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140461955,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461955,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461957,"feature_type":"variation","strand":1,"end":140461957,"alleles":["T","C"],"clinical_significance":[],"id":"rs1794632588","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1794632642","clinical_significance":[],"alleles":["G","A"],"end":140461958,"strand":1,"feature_type":"variation","start":140461958,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140461959,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140461959,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs192510427","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140461967,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461967,"clinical_significance":[],"seq_region_name":"7","id":"rs1005847362"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585473183","feature_type":"variation","strand":1,"end":140461975,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461975},{"clinical_significance":[],"id":"rs1794633457","seq_region_name":"7","source":"dbSNP","start":140461976,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140461976,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1298846458","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140461977,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461977},{"start":140461980,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140461980,"strand":1,"feature_type":"variation","id":"rs1016269553","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs577350751","seq_region_name":"7","feature_type":"variation","strand":1,"end":140461981,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461981},{"seq_region_name":"7","id":"rs1385464497","clinical_significance":[],"start":140461982,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140461982,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs182271042","clinical_significance":[],"alleles":["C","G","T"],"end":140461983,"strand":1,"feature_type":"variation","start":140461983,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140461983,"alleles":["-","AAAAG"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140461984,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794634361"},{"clinical_significance":[],"seq_region_name":"7","id":"rs7786843","feature_type":"variation","strand":1,"end":140461984,"alleles":["G","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461984},{"seq_region_name":"7","id":"rs377044537","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461984,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GAAAG","-"],"end":140461988},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461985,"source":"dbSNP","strand":1,"feature_type":"variation","end":140461985,"alleles":["A","C"],"id":"rs1794634626","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461985,"source":"dbSNP","strand":1,"feature_type":"variation","end":140461999,"alleles":["AAAGAAAAGAAAAGA","AAAGAAAAGA"],"seq_region_name":"7","id":"rs1015720894","clinical_significance":[]},{"alleles":["AAAA","AAAAA"],"end":140461992,"strand":1,"feature_type":"variation","start":140461989,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs897274729","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140461990,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140461990,"seq_region_name":"7","id":"rs1794634966","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140461993,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140461993,"clinical_significance":[],"seq_region_name":"7","id":"rs1794635017"},{"seq_region_name":"7","id":"rs1432500825","clinical_significance":[],"start":140461994,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AAAA","AA"],"end":140461997,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140461995,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140461995,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1374581494"},{"seq_region_name":"7","id":"rs1794635179","clinical_significance":[],"start":140461999,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140461999,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462002,"source":"dbSNP","strand":1,"feature_type":"variation","end":140462002,"alleles":["A","G"],"id":"rs1794635234","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794635290","source":"dbSNP","start":140462004,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140462004,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462004,"feature_type":"variation","strand":1,"alleles":["TATCACAAT","TATCACAATATCACAAT"],"end":140462012,"clinical_significance":[],"seq_region_name":"7","id":"rs1794635334"},{"alleles":["T","A","C"],"end":140462006,"strand":1,"feature_type":"variation","start":140462006,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1229143425","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794635468","source":"dbSNP","start":140462014,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140462014,"alleles":["C","A"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462018,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140462018,"seq_region_name":"7","id":"rs1170881569","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140462027,"alleles":["ATTTTA","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462022,"clinical_significance":[],"seq_region_name":"7","id":"rs1794635583"},{"id":"rs1794635640","seq_region_name":"7","clinical_significance":[],"start":140462025,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140462025,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140462028,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462028,"source":"dbSNP","seq_region_name":"7","id":"rs1430226257","clinical_significance":[]},{"source":"dbSNP","start":140462034,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140462034,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1417375914"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462038,"feature_type":"variation","strand":1,"end":140462038,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs556684652"},{"feature_type":"variation","strand":1,"end":140462040,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462040,"clinical_significance":[],"seq_region_name":"7","id":"rs542525566"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140462046,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462046,"clinical_significance":[],"seq_region_name":"7","id":"rs1030298672"},{"seq_region_name":"7","id":"rs1208954214","clinical_significance":[],"strand":1,"feature_type":"variation","end":140462051,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462051,"source":"dbSNP"},{"start":140462051,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140462055,"alleles":["AGAGA","AGA"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1259730249","clinical_significance":[]},{"end":140462054,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140462054,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794636119"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794636155","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140462056,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462056},{"alleles":["C","T"],"end":140462058,"feature_type":"variation","strand":1,"source":"dbSNP","start":140462058,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1794636229","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1794636283","seq_region_name":"7","source":"dbSNP","start":140462060,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["CTCT","CT"],"end":140462063,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs954307124","clinical_significance":[],"alleles":["T","C"],"end":140462061,"strand":1,"feature_type":"variation","start":140462061,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1794636390","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["-","G"],"end":140462063,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462064,"source":"dbSNP"},{"alleles":["A","G"],"end":140462064,"feature_type":"variation","strand":1,"source":"dbSNP","start":140462064,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1794636443","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140462070,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462070,"clinical_significance":[],"seq_region_name":"7","id":"rs1316677664"},{"seq_region_name":"7","id":"rs1485472793","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462073,"source":"dbSNP","strand":1,"feature_type":"variation","end":140462073,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs986223161","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462075,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140462075},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462077,"feature_type":"variation","strand":1,"end":140462077,"alleles":["G","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585473371"},{"end":140462080,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140462080,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794636704","clinical_significance":[]},{"seq_region_name":"7","id":"rs1017277209","clinical_significance":[],"end":140462081,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140462081,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140462083,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462083,"source":"dbSNP","seq_region_name":"7","id":"rs561260123","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs578098949","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462084,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140462084},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462085,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140462085,"clinical_significance":[],"seq_region_name":"7","id":"rs1585473398"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462086,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140462086,"seq_region_name":"7","id":"rs1794637012","clinical_significance":[]},{"end":140462087,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140462087,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794637067"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140462088,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462088,"clinical_significance":[],"id":"rs1181131893","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs954773674","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140462089,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462089},{"seq_region_name":"7","id":"rs1262148955","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462090,"source":"dbSNP","strand":1,"feature_type":"variation","end":140462090,"alleles":["T","C"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462099,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140462099,"seq_region_name":"7","id":"rs1355486286","clinical_significance":[]},{"clinical_significance":[],"id":"rs957808957","seq_region_name":"7","alleles":["A","G"],"end":140462102,"feature_type":"variation","strand":1,"source":"dbSNP","start":140462102,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140462107,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462107,"clinical_significance":[],"seq_region_name":"7","id":"rs1412467109"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462112,"feature_type":"variation","strand":1,"end":140462112,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs986300524"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794637730","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140462113,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462113},{"seq_region_name":"7","id":"rs1794637810","clinical_significance":[],"strand":1,"feature_type":"variation","end":140462118,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462118,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1421615090","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140462120,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462120,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130280436","feature_type":"variation","strand":1,"end":140462130,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462130},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462131,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140462131,"clinical_significance":[],"seq_region_name":"7","id":"rs910710575"},{"source":"dbSNP","start":140462132,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140462132,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1298529345"},{"seq_region_name":"7","id":"rs1463370725","clinical_significance":[],"start":140462134,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140462134,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs989197072","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140462135,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462135,"source":"dbSNP"},{"alleles":["G","A","T"],"end":140462136,"feature_type":"variation","strand":1,"source":"dbSNP","start":140462136,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs969001805"},{"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140462139,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462139,"clinical_significance":[],"seq_region_name":"7","id":"rs979402454"},{"clinical_significance":[],"seq_region_name":"7","id":"rs982066999","end":140462140,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140462140,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140462142,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140462142,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794638583"},{"clinical_significance":[],"id":"rs1794638695","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","T"],"end":140462145,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462145},{"alleles":["C","G"],"end":140462147,"feature_type":"variation","strand":1,"source":"dbSNP","start":140462147,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs545712021"},{"seq_region_name":"7","id":"rs1794638908","clinical_significance":[],"alleles":["CCTCCT","CCTCCTCCT"],"end":140462152,"strand":1,"feature_type":"variation","start":140462147,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs186938029","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","C","T"],"end":140462153,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462153,"source":"dbSNP"},{"end":140462158,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140462158,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs113348418"},{"source":"dbSNP","start":140462162,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140462162,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794639303"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462165,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140462165,"seq_region_name":"7","id":"rs917043425","clinical_significance":[]},{"seq_region_name":"7","id":"rs540457157","clinical_significance":[],"end":140462166,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140462166,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462169,"feature_type":"variation","strand":1,"end":140462169,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794639527"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140462171,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462171,"clinical_significance":[],"seq_region_name":"7","id":"rs948444326"},{"seq_region_name":"7","id":"rs1383567477","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462175,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140462175},{"start":140462176,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140462176,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs565226696","clinical_significance":[]},{"start":140462179,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140462179,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1337589469","clinical_significance":[]},{"seq_region_name":"7","id":"rs1274440612","clinical_significance":[],"strand":1,"feature_type":"variation","end":140462180,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462180,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs888238244","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462182,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140462182},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140462184,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462184,"source":"dbSNP","seq_region_name":"7","id":"rs368750212","clinical_significance":[]},{"alleles":["G","A","T"],"end":140462185,"feature_type":"variation","strand":1,"source":"dbSNP","start":140462185,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs551099053","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs569234135","alleles":["C","A"],"end":140462186,"feature_type":"variation","strand":1,"source":"dbSNP","start":140462186,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140462189,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140462189,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","id":"rs1794640202","seq_region_name":"7","clinical_significance":[]},{"end":140462190,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140462190,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794640274"},{"id":"rs530132845","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462191,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140462191},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462191,"source":"dbSNP","strand":1,"feature_type":"variation","end":140462196,"alleles":["CTAACT","CT"],"id":"rs1794640394","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140462192,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140462192,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1310426985"},{"seq_region_name":"7","id":"rs1794640508","clinical_significance":[],"strand":1,"feature_type":"variation","end":140462195,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462195,"source":"dbSNP"},{"seq_region_name":"7","id":"rs993481782","clinical_significance":[],"strand":1,"feature_type":"variation","end":140462196,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462196,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462196,"source":"dbSNP","strand":1,"feature_type":"variation","end":140462202,"alleles":["TTTTTTT","TTTTTT","TTTTTTTT"],"id":"rs1297401083","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140462199,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140462199,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794640706"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462201,"source":"dbSNP","strand":1,"feature_type":"variation","end":140462205,"alleles":["TTATT","TT"],"id":"rs1162870121","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462202,"feature_type":"variation","strand":1,"end":140462202,"alleles":["T","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794640893"},{"start":140462203,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140462203,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs760157707","clinical_significance":[]},{"clinical_significance":[],"id":"rs1261097807","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462204,"feature_type":"variation","strand":1,"end":140462204,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1461021318","feature_type":"variation","strand":1,"end":140462209,"alleles":["TTTTTT","TTTTTTT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462204},{"end":140462207,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140462207,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794641272","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140462210,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462210,"source":"dbSNP","seq_region_name":"7","id":"rs954824148","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794641434","clinical_significance":[],"start":140462215,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140462215,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140462217,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462217,"clinical_significance":[],"id":"rs1794641541","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462218,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140462218,"clinical_significance":[],"seq_region_name":"7","id":"rs1794641638"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462226,"feature_type":"variation","strand":1,"end":140462226,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794641739"},{"clinical_significance":[],"id":"rs764267297","seq_region_name":"7","feature_type":"variation","strand":1,"end":140462229,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462229},{"clinical_significance":[],"seq_region_name":"7","id":"rs1219099661","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462230,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140462230},{"strand":1,"feature_type":"variation","end":140462237,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462237,"source":"dbSNP","id":"rs1794642019","seq_region_name":"7","clinical_significance":[]},{"alleles":["GG","GGG"],"end":140462240,"strand":1,"feature_type":"variation","start":140462239,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130281175","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794642114","clinical_significance":[],"end":140462245,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140462245,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462248,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140462248,"clinical_significance":[],"id":"rs753119671","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1250170921","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140462251,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462251,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs75932038","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140462254,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462254},{"seq_region_name":"7","id":"rs1794642573","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140462260,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462260,"source":"dbSNP"},{"source":"dbSNP","start":140462263,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140462263,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1200313091"},{"start":140462266,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140462266,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794642778","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794642862","clinical_significance":[],"start":140462266,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140462266,"alleles":["C","CC"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1251726303","clinical_significance":[],"end":140462269,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140462269,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794643049","source":"dbSNP","start":140462270,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140462270,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794643141","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462273,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140462273},{"alleles":["C","T"],"end":140462274,"strand":1,"feature_type":"variation","start":140462274,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1211253957","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1487846091","clinical_significance":[],"alleles":["T","C"],"end":140462280,"strand":1,"feature_type":"variation","start":140462280,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140462283,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140462283,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs957654211"},{"end":140462288,"alleles":["CCC","CC"],"strand":1,"feature_type":"variation","start":140462286,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1240659261","seq_region_name":"7","clinical_significance":[]},{"id":"rs2130281385","seq_region_name":"7","clinical_significance":[],"start":140462287,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140462287,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140462289,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C","G"],"end":140462289,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs7808589","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1794643617","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["AAA","A"],"end":140462291,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462289,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1306011571","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462293,"feature_type":"variation","strand":1,"end":140462293,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1794643813","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462295,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140462295},{"seq_region_name":"7","id":"rs77824866","clinical_significance":[],"end":140462296,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140462296,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140462298,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140462298,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794644018","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462299,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140462299,"seq_region_name":"7","id":"rs2130281504","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794644130","clinical_significance":[],"start":140462300,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140462300,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"end":140462302,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140462302,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1373049114"},{"seq_region_name":"7","id":"rs1794644304","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140462306,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462306,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1323860972","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462309,"source":"dbSNP","strand":1,"feature_type":"variation","end":140462309,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1032365161","feature_type":"variation","strand":1,"alleles":["C","A","G","T"],"end":140462310,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462310},{"clinical_significance":[],"seq_region_name":"7","id":"rs1346194851","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462311,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140462311},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794644737","feature_type":"variation","strand":1,"end":140462313,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462313},{"start":140462316,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140462316,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs368647793","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs956314478","alleles":["G","A","C"],"end":140462317,"feature_type":"variation","strand":1,"source":"dbSNP","start":140462317,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462318,"source":"dbSNP","strand":1,"feature_type":"variation","end":140462318,"alleles":["G","A"],"seq_region_name":"7","id":"rs374700056","clinical_significance":[]},{"clinical_significance":[],"id":"rs916884902","seq_region_name":"7","source":"dbSNP","start":140462324,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140462324,"alleles":["C","A","G","T"],"feature_type":"variation","strand":1},{"id":"rs559145356","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140462325,"strand":1,"feature_type":"variation","start":140462325,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794645425","source":"dbSNP","start":140462326,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140462326,"feature_type":"variation","strand":1},{"id":"rs1794645517","seq_region_name":"7","clinical_significance":[],"start":140462327,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140462327,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs571004491","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140462328,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462328,"source":"dbSNP"},{"alleles":["T","C"],"end":140462331,"feature_type":"variation","strand":1,"source":"dbSNP","start":140462331,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs979823889"},{"id":"rs1794645790","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462332,"source":"dbSNP","strand":1,"feature_type":"variation","end":140462332,"alleles":["A","C"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462334,"feature_type":"variation","strand":1,"end":140462334,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794645869"},{"strand":1,"feature_type":"variation","end":140462340,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462340,"source":"dbSNP","seq_region_name":"7","id":"rs2130281771","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794645968","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462341,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140462341},{"start":140462344,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140462344,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1364792879","clinical_significance":[]},{"clinical_significance":[],"id":"rs764270011","seq_region_name":"7","feature_type":"variation","strand":1,"end":140462346,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462346},{"clinical_significance":[],"seq_region_name":"7","id":"rs538298064","alleles":["A","G"],"end":140462347,"feature_type":"variation","strand":1,"source":"dbSNP","start":140462347,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1794646366","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462350,"source":"dbSNP","strand":1,"feature_type":"variation","end":140462350,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1448089070","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462351,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140462351},{"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140462352,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462352,"source":"dbSNP","seq_region_name":"7","id":"rs146484032","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140462357,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462357,"source":"dbSNP","seq_region_name":"7","id":"rs2130281885","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1206440930","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462359,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140462359},{"id":"rs574868421","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140462360,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462360,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1318631077","source":"dbSNP","start":140462361,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140462361,"alleles":["T","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130281926","feature_type":"variation","strand":1,"end":140462362,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462362},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140462363,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462363,"source":"dbSNP","seq_region_name":"7","id":"rs767879173","clinical_significance":[]},{"seq_region_name":"7","id":"rs1237742365","clinical_significance":[],"start":140462364,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140462364,"strand":1,"feature_type":"variation"},{"id":"rs990656546","seq_region_name":"7","clinical_significance":[],"start":140462367,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140462367,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"id":"rs1284911496","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462368,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140462368},{"alleles":["TTT","TT"],"end":140462370,"feature_type":"variation","strand":1,"source":"dbSNP","start":140462368,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794647224"},{"feature_type":"variation","strand":1,"end":140462372,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462372,"clinical_significance":[],"seq_region_name":"7","id":"rs1794647326"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140462374,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462374,"source":"dbSNP","seq_region_name":"7","id":"rs2130282038","clinical_significance":[]},{"clinical_significance":[],"id":"rs1794647410","seq_region_name":"7","source":"dbSNP","start":140462377,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140462377,"alleles":["G","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794647499","source":"dbSNP","start":140462378,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140462378,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1794647590","seq_region_name":"7","source":"dbSNP","start":140462381,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140462381,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140462382,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462382,"clinical_significance":[],"id":"rs1794647699","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1211299777","clinical_significance":[],"start":140462382,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140462384,"alleles":["ATA","A"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462385,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140462385,"seq_region_name":"7","id":"rs1585473922","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462388,"feature_type":"variation","strand":1,"end":140462391,"alleles":["TATA","TA"],"clinical_significance":[],"seq_region_name":"7","id":"rs1285040059"},{"seq_region_name":"7","id":"rs909902302","clinical_significance":[],"start":140462390,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140462390,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs539801195","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462391,"feature_type":"variation","strand":1,"end":140462391,"alleles":["A","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794648275","end":140462392,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140462392,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1232356999","clinical_significance":[],"start":140462392,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["GTTTGTTATCAAGTGGTT","GTT"],"end":140462409,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1563090164","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462393,"source":"dbSNP","strand":1,"feature_type":"variation","end":140462393,"alleles":["T","C"]},{"start":140462394,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140462398,"alleles":["TTGTT","TT"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1248534689","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130282243","clinical_significance":[],"strand":1,"feature_type":"variation","end":140462397,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462397,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462400,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140462400,"clinical_significance":[],"seq_region_name":"7","id":"rs1036980574"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462401,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140462401,"id":"rs1487525094","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462404,"source":"dbSNP","strand":1,"feature_type":"variation","end":140462404,"alleles":["G","A"],"seq_region_name":"7","id":"rs1783762529","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462414,"feature_type":"variation","strand":1,"end":140462414,"alleles":["T","A"],"clinical_significance":[],"id":"rs1794649056","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140462417,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462417,"source":"dbSNP","seq_region_name":"7","id":"rs1794649129","clinical_significance":[]},{"clinical_significance":[],"id":"rs2130282330","seq_region_name":"7","end":140462418,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140462418,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1313663298","clinical_significance":[],"alleles":["A","G"],"end":140462419,"strand":1,"feature_type":"variation","start":140462419,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462423,"feature_type":"variation","strand":1,"end":140462423,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1944097101"},{"alleles":["A","T"],"end":140462429,"feature_type":"variation","strand":1,"source":"dbSNP","start":140462429,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794649305"},{"feature_type":"variation","strand":1,"end":140462434,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462434,"clinical_significance":[],"id":"rs1436852628","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs755586695","source":"dbSNP","start":140462438,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140462438,"alleles":["T","-"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462441,"feature_type":"variation","strand":1,"end":140462441,"alleles":["T","C"],"clinical_significance":[],"id":"rs1173424214","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462444,"feature_type":"variation","strand":1,"end":140462444,"alleles":["G","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794649641"},{"feature_type":"variation","strand":1,"end":140462445,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462445,"clinical_significance":[],"seq_region_name":"7","id":"rs1409421770"},{"clinical_significance":[],"id":"rs1036848001","seq_region_name":"7","alleles":["G","A"],"end":140462446,"feature_type":"variation","strand":1,"source":"dbSNP","start":140462446,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140462449,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","-"],"end":140462449,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794649896"},{"strand":1,"feature_type":"variation","end":140462450,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462450,"source":"dbSNP","seq_region_name":"7","id":"rs2130282468","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794649989","feature_type":"variation","strand":1,"end":140462451,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462451},{"end":140462452,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140462452,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794650082","clinical_significance":[]},{"id":"rs144862274","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140462453,"strand":1,"feature_type":"variation","start":140462453,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1194652746","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140462455,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462455},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462456,"source":"dbSNP","strand":1,"feature_type":"variation","end":140462456,"alleles":["C","A"],"seq_region_name":"7","id":"rs1794650371","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462459,"feature_type":"variation","strand":1,"end":140462459,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794650469"},{"seq_region_name":"7","id":"rs933900752","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462460,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140462460},{"end":140462461,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140462461,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585474056","clinical_significance":[]},{"id":"rs1794650750","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140462464,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462464,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1426265938","alleles":["T","A","C"],"end":140462466,"feature_type":"variation","strand":1,"source":"dbSNP","start":140462466,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1188170900","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462467,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140462467},{"clinical_significance":[],"seq_region_name":"7","id":"rs1610271","feature_type":"variation","strand":1,"end":140462468,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462468},{"end":140462469,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140462469,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs113276142"},{"feature_type":"variation","strand":1,"end":140462475,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462475,"clinical_significance":[],"seq_region_name":"7","id":"rs1794651307"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794651401","feature_type":"variation","strand":1,"alleles":["TAAAGTAAA","TAAA"],"end":140462484,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462476},{"id":"rs1794651484","seq_region_name":"7","clinical_significance":[],"end":140462477,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140462477,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["AAA","AAAA"],"end":140462479,"strand":1,"feature_type":"variation","start":140462477,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794651568","clinical_significance":[]},{"source":"dbSNP","start":140462481,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","TT"],"end":140462481,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1051734189"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462481,"feature_type":"variation","strand":1,"alleles":["T","-"],"end":140462481,"clinical_significance":[],"id":"rs1794651752","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1794651851","clinical_significance":[],"start":140462482,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140462482,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"id":"rs1007614434","seq_region_name":"7","clinical_significance":[],"end":140462496,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140462496,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140462498,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462498,"source":"dbSNP","seq_region_name":"7","id":"rs1794652011","clinical_significance":[]},{"seq_region_name":"7","id":"rs1253058345","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462501,"source":"dbSNP","strand":1,"feature_type":"variation","end":140462501,"alleles":["T","C","G"]},{"source":"dbSNP","start":140462504,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140462504,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130282832"},{"alleles":["C","A","T"],"end":140462505,"strand":1,"feature_type":"variation","start":140462505,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1424905071","clinical_significance":[]},{"clinical_significance":[],"id":"rs1794652291","seq_region_name":"7","end":140462506,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140462506,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794652357","alleles":["G","A"],"end":140462515,"feature_type":"variation","strand":1,"source":"dbSNP","start":140462515,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1293990761","feature_type":"variation","strand":1,"alleles":["GC","-"],"end":140462516,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462515},{"seq_region_name":"7","id":"rs1585474136","clinical_significance":[],"strand":1,"feature_type":"variation","end":140462516,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462516,"source":"dbSNP"},{"source":"dbSNP","start":140462519,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140462519,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1416794848","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462529,"source":"dbSNP","strand":1,"feature_type":"variation","end":140462529,"alleles":["G","A"],"seq_region_name":"7","id":"rs1018136157","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794652785","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462531,"feature_type":"variation","strand":1,"end":140462531,"alleles":["G","A"]},{"end":140462533,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140462533,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs889928714","clinical_significance":[]},{"clinical_significance":[],"id":"rs374449569","seq_region_name":"7","source":"dbSNP","start":140462534,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140462534,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140462537,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462537,"clinical_significance":[],"seq_region_name":"7","id":"rs1794653051"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462538,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140462538,"clinical_significance":[],"seq_region_name":"7","id":"rs1794653134"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794653227","end":140462541,"alleles":["-","TTAC"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140462542,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1794653318","clinical_significance":[],"start":140462542,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140462542,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462546,"feature_type":"variation","strand":1,"end":140462547,"alleles":["TT","-"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794653408"},{"end":140462547,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140462547,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs904589618","seq_region_name":"7"},{"start":140462548,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140462548,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1165042381","clinical_significance":[]},{"seq_region_name":"7","id":"rs1399227167","clinical_significance":[],"strand":1,"feature_type":"variation","end":140462557,"alleles":["TTATTATTA","TTATTA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462549,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1794653804","clinical_significance":[],"strand":1,"feature_type":"variation","end":140462551,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462551,"source":"dbSNP"},{"end":140462552,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140462552,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794653852"},{"seq_region_name":"7","id":"rs1347633565","clinical_significance":[],"end":140462553,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140462553,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140462554,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140462554,"alleles":["A","G"],"strand":1,"feature_type":"variation","id":"rs1794653963","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140462555,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462555,"clinical_significance":[],"seq_region_name":"7","id":"rs1166610891"},{"clinical_significance":[],"seq_region_name":"7","id":"rs893489555","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462557,"feature_type":"variation","strand":1,"end":140462557,"alleles":["A","C"]},{"seq_region_name":"7","id":"rs2130283174","clinical_significance":[],"end":140462561,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140462561,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462565,"feature_type":"variation","strand":1,"end":140462565,"alleles":["C","T"],"clinical_significance":[],"id":"rs1422200079","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1010608225","clinical_significance":[],"alleles":["A","G"],"end":140462566,"strand":1,"feature_type":"variation","start":140462566,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1000812028","seq_region_name":"7","clinical_significance":[],"end":140462574,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140462574,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140462576,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140462576,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1255043003","seq_region_name":"7"},{"source":"dbSNP","start":140462578,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140462578,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794654352"},{"strand":1,"feature_type":"variation","end":140462579,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462579,"source":"dbSNP","id":"rs1186541402","seq_region_name":"7","clinical_significance":[]},{"end":140462583,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140462583,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1298220179"},{"clinical_significance":[],"id":"rs1794654524","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462585,"feature_type":"variation","strand":1,"end":140462585,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794654582","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462589,"feature_type":"variation","strand":1,"end":140462589,"alleles":["G","A"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462595,"feature_type":"variation","strand":1,"end":140462595,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794654669"},{"id":"rs1794654755","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140462598,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462598,"source":"dbSNP"},{"source":"dbSNP","start":140462600,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140462600,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs966902790","seq_region_name":"7"},{"alleles":["G","A"],"end":140462602,"feature_type":"variation","strand":1,"source":"dbSNP","start":140462602,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794654967"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462603,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140462603,"clinical_significance":[],"seq_region_name":"7","id":"rs184043997"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794655090","source":"dbSNP","start":140462605,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140462605,"alleles":["G","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs956283472","clinical_significance":[],"end":140462606,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140462606,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1794655184","clinical_significance":[],"start":140462607,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140462607,"strand":1,"feature_type":"variation"},{"end":140462609,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140462609,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1317237651","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585474263","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462610,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140462610},{"clinical_significance":[],"seq_region_name":"7","id":"rs1273878644","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462615,"feature_type":"variation","strand":1,"end":140462615,"alleles":["G","A"]},{"alleles":["GCTCAGGGGTTAGAGACAAGCCTGGGC","GC"],"end":140462641,"strand":1,"feature_type":"variation","start":140462615,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1359805694","clinical_significance":[]},{"alleles":["C","T"],"end":140462616,"strand":1,"feature_type":"variation","start":140462616,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1235291367","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1332920792","feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140462622,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462622},{"seq_region_name":"7","id":"rs1563090274","clinical_significance":[],"strand":1,"feature_type":"variation","end":140462623,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462623,"source":"dbSNP"},{"source":"dbSNP","start":140462629,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140462629,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1283869059"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462644,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140462644,"id":"rs1794655683","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794655729","alleles":["A","G"],"end":140462645,"feature_type":"variation","strand":1,"source":"dbSNP","start":140462645,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1794655771","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462646,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140462646},{"clinical_significance":[],"seq_region_name":"7","id":"rs993041686","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462649,"feature_type":"variation","strand":1,"end":140462649,"alleles":["C","T"]},{"id":"rs1337860279","seq_region_name":"7","clinical_significance":[],"alleles":["A","G"],"end":140462652,"strand":1,"feature_type":"variation","start":140462652,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1327271072","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462655,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140462655},{"clinical_significance":[],"seq_region_name":"7","id":"rs1023995314","source":"dbSNP","start":140462657,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140462657,"feature_type":"variation","strand":1},{"alleles":["G","A","C"],"end":140462658,"feature_type":"variation","strand":1,"source":"dbSNP","start":140462658,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1395926131"},{"end":140462659,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140462659,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1794656125","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1794656167","seq_region_name":"7","feature_type":"variation","strand":1,"end":140462660,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462660},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794656216","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462664,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140462664},{"seq_region_name":"7","id":"rs2130283758","clinical_significance":[],"alleles":["ACTAAAAATAAAAAAATTA","-"],"end":140462682,"strand":1,"feature_type":"variation","start":140462664,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140462665,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462665,"clinical_significance":[],"seq_region_name":"7","id":"rs969683846"},{"id":"rs990708752","seq_region_name":"7","clinical_significance":[],"end":140462666,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140462666,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140462667,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462667,"clinical_significance":[],"seq_region_name":"7","id":"rs565026820"},{"clinical_significance":[],"id":"rs532357170","seq_region_name":"7","alleles":["A","G"],"end":140462668,"feature_type":"variation","strand":1,"source":"dbSNP","start":140462668,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140462672,"alleles":["T","A","C","G"],"strand":1,"feature_type":"variation","start":140462672,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1969394","clinical_significance":[]},{"start":140462673,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AAAAAAA","AAAAAAAA"],"end":140462679,"strand":1,"feature_type":"variation","id":"rs1794656658","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462675,"source":"dbSNP","strand":1,"feature_type":"variation","end":140462675,"alleles":["A","C"],"seq_region_name":"7","id":"rs941115845","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794656766","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462676,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140462676},{"clinical_significance":[],"seq_region_name":"7","id":"rs973010721","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462681,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140462681},{"source":"dbSNP","start":140462683,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140462683,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs372215010"},{"alleles":["A","C"],"end":140462686,"strand":1,"feature_type":"variation","start":140462686,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130283949","clinical_significance":[]},{"clinical_significance":[],"id":"rs933910624","seq_region_name":"7","end":140462690,"alleles":["C","A","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140462690,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs562992317","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140462691,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462691,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794657093","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462693,"feature_type":"variation","strand":1,"end":140462693,"alleles":["A","G"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462694,"source":"dbSNP","strand":1,"feature_type":"variation","end":140462694,"alleles":["G","C"],"id":"rs2130284011","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462697,"source":"dbSNP","strand":1,"feature_type":"variation","end":140462697,"alleles":["G","A"],"id":"rs1794657151","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462699,"feature_type":"variation","strand":1,"alleles":["TCACGCCTGTAATCCCAGCATTTTGGGAGGCTGAGGTGGGTGGATCACG","TCACG"],"end":140462747,"clinical_significance":[],"id":"rs1794657193","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462700,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140462700,"id":"rs1794657248","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794657306","clinical_significance":[],"end":140462702,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140462702,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462703,"feature_type":"variation","strand":1,"end":140462703,"alleles":["G","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs530578114"},{"feature_type":"variation","strand":1,"end":140462704,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462704,"clinical_significance":[],"id":"rs1794657435","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462709,"feature_type":"variation","strand":1,"end":140462709,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs918587693"},{"id":"rs1794657545","seq_region_name":"7","clinical_significance":[],"end":140462711,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140462711,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794657598","source":"dbSNP","start":140462716,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140462716,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1289279939","clinical_significance":[],"start":140462718,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140462718,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140462719,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140462719,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1459488222"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462726,"source":"dbSNP","strand":1,"feature_type":"variation","end":140462726,"alleles":["A","T"],"id":"rs1224476590","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140462728,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140462728,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1585474414","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140462729,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462729,"clinical_significance":[],"seq_region_name":"7","id":"rs934075642"},{"seq_region_name":"7","id":"rs1177239385","clinical_significance":[],"start":140462730,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140462730,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1237985720","clinical_significance":[],"strand":1,"feature_type":"variation","end":140462731,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462731,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1278131378","source":"dbSNP","start":140462734,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140462734,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1794659101","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462735,"source":"dbSNP","strand":1,"feature_type":"variation","end":140462735,"alleles":["T","C"]},{"source":"dbSNP","start":140462739,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140462739,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs943398572"},{"seq_region_name":"7","id":"rs1039033177","clinical_significance":[],"start":140462743,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140462743,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1165340878","feature_type":"variation","strand":1,"end":140462744,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462744},{"end":140462746,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140462746,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1328577329","clinical_significance":[]},{"start":140462747,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140462747,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","id":"rs753337639","seq_region_name":"7","clinical_significance":[]},{"id":"rs1794659489","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140462754,"strand":1,"feature_type":"variation","start":140462754,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1794659540","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140462755,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462755},{"alleles":["A","T"],"end":140462758,"strand":1,"feature_type":"variation","start":140462758,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794659600","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462760,"feature_type":"variation","strand":1,"end":140462760,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1000252789"},{"seq_region_name":"7","id":"rs188313548","clinical_significance":[],"start":140462761,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140462761,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs192819185","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462768,"feature_type":"variation","strand":1,"alleles":["T","A","C","G"],"end":140462768},{"source":"dbSNP","start":140462768,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TCCTGGCT","T"],"end":140462775,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794659878"},{"start":140462773,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140462773,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1464006032","clinical_significance":[]},{"end":140462775,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140462775,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794659985","clinical_significance":[]},{"seq_region_name":"7","id":"rs1330549133","clinical_significance":[],"start":140462777,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140462781,"alleles":["ACACG","-"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462779,"source":"dbSNP","strand":1,"feature_type":"variation","end":140462779,"alleles":["A","G"],"seq_region_name":"7","id":"rs1383289541","clinical_significance":[]},{"clinical_significance":[],"id":"rs1454423697","seq_region_name":"7","alleles":["C","G","T"],"end":140462780,"feature_type":"variation","strand":1,"source":"dbSNP","start":140462780,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140462781,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140462781,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1452501777"},{"alleles":["G","T"],"end":140462782,"strand":1,"feature_type":"variation","start":140462782,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1282185875","clinical_significance":[]},{"source":"dbSNP","start":140462783,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140462783,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794660320"},{"clinical_significance":[],"seq_region_name":"7","id":"rs891946445","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140462787,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462787},{"start":140462788,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140462791,"alleles":["CCCC","CCCCC"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794660430","clinical_significance":[]},{"seq_region_name":"7","id":"rs1448953939","clinical_significance":[],"alleles":["C","T"],"end":140462790,"strand":1,"feature_type":"variation","start":140462790,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs550248048","clinical_significance":[],"strand":1,"feature_type":"variation","end":140462791,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462791,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1024591959","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462792,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140462792},{"seq_region_name":"7","id":"rs1794660680","clinical_significance":[],"alleles":["C","G"],"end":140462796,"strand":1,"feature_type":"variation","start":140462796,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1320040849","seq_region_name":"7","source":"dbSNP","start":140462798,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140462798,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794660793","alleles":["C","A","T"],"end":140462799,"feature_type":"variation","strand":1,"source":"dbSNP","start":140462799,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs970278215","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140462800,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462800,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462801,"feature_type":"variation","strand":1,"end":140462806,"alleles":["AAAAAA","AAAAA","AAAAAAA"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794661101"},{"seq_region_name":"7","id":"rs1367587525","clinical_significance":[],"start":140462807,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140462807,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462809,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140462809,"seq_region_name":"7","id":"rs1001646523","clinical_significance":[]},{"start":140462813,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140462813,"alleles":["A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794661355","clinical_significance":[]},{"id":"rs75106034","seq_region_name":"7","clinical_significance":[],"end":140462818,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","start":140462818,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1430872941","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462822,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140462822},{"start":140462823,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140462823,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs111797775","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1418749213","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462824,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140462824},{"strand":1,"feature_type":"variation","end":140462825,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462825,"source":"dbSNP","seq_region_name":"7","id":"rs1585474601","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462826,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140462826,"seq_region_name":"7","id":"rs962784226","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462827,"feature_type":"variation","strand":1,"end":140462827,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs902143750"},{"id":"rs1175301284","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462831,"source":"dbSNP","strand":1,"feature_type":"variation","end":140462831,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1412676246","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462832,"source":"dbSNP","strand":1,"feature_type":"variation","end":140462832,"alleles":["G","C"]},{"seq_region_name":"7","id":"rs1794661949","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462833,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140462833},{"alleles":["T","C"],"end":140462834,"strand":1,"feature_type":"variation","start":140462834,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1424457694","clinical_significance":[]},{"end":140462835,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140462835,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1794662214","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140462836,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462836,"source":"dbSNP","seq_region_name":"7","id":"rs1794662268","clinical_significance":[]},{"source":"dbSNP","start":140462838,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140462838,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1003721501"},{"id":"rs748010536","seq_region_name":"7","clinical_significance":[],"start":140462839,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140462839,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1794662450","clinical_significance":[],"start":140462840,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140462840,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs959099841","source":"dbSNP","start":140462848,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140462848,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1794662566","clinical_significance":[],"end":140462849,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140462849,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140462851,"alleles":["A","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140462851,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1193133487"},{"seq_region_name":"7","id":"rs1794662686","clinical_significance":[],"strand":1,"feature_type":"variation","end":140462851,"alleles":["A","AAAA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462851,"source":"dbSNP"},{"source":"dbSNP","start":140462852,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140462852,"alleles":["C","A","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1381118840"},{"clinical_significance":[],"seq_region_name":"7","id":"rs552594994","feature_type":"variation","strand":1,"end":140462855,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462855},{"end":140462865,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140462865,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1209261168"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462866,"feature_type":"variation","strand":1,"end":140462866,"alleles":["T","A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs918435469"},{"source":"dbSNP","start":140462872,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140462879,"alleles":["ACAAGAAT","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794662937"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1274378104","feature_type":"variation","strand":1,"end":140462873,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462873},{"clinical_significance":[],"seq_region_name":"7","id":"rs1012057995","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462874,"feature_type":"variation","strand":1,"end":140462874,"alleles":["A","G"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462876,"source":"dbSNP","strand":1,"feature_type":"variation","end":140462876,"alleles":["G","A"],"seq_region_name":"7","id":"rs955239112","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["AAT","-"],"end":140462879,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462877,"source":"dbSNP","seq_region_name":"7","id":"rs35688062","clinical_significance":[]},{"id":"rs1794663220","seq_region_name":"7","clinical_significance":[],"start":140462880,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140462880,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"start":140462883,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140462883,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794663287","clinical_significance":[]},{"seq_region_name":"7","id":"rs1275767102","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462885,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140462885},{"clinical_significance":[],"id":"rs1398946781","seq_region_name":"7","end":140462886,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140462886,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140462888,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462888,"source":"dbSNP","seq_region_name":"7","id":"rs1794663456","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs570668535","alleles":["C","T"],"end":140462897,"feature_type":"variation","strand":1,"source":"dbSNP","start":140462897,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140462898,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140462898,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs769755314"},{"alleles":["G","A"],"end":140462899,"feature_type":"variation","strand":1,"source":"dbSNP","start":140462899,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1314488569"},{"start":140462902,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140462902,"strand":1,"feature_type":"variation","id":"rs962635464","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794663738","end":140462905,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140462905,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","T"],"end":140462906,"strand":1,"feature_type":"variation","start":140462906,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs185290201","seq_region_name":"7","clinical_significance":[]},{"start":140462907,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140462907,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs942625773","clinical_significance":[]},{"clinical_significance":[],"id":"rs2130285343","seq_region_name":"7","end":140462910,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140462910,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1794663947","seq_region_name":"7","clinical_significance":[],"start":140462916,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140462916,"strand":1,"feature_type":"variation"},{"start":140462917,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140462917,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1411595168","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140462920,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462920,"clinical_significance":[],"seq_region_name":"7","id":"rs1039454474"},{"seq_region_name":"7","id":"rs569064342","clinical_significance":[],"end":140462921,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140462921,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462924,"feature_type":"variation","strand":1,"end":140462924,"alleles":["C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1186679126"},{"end":140462933,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140462933,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794664321"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462939,"source":"dbSNP","strand":1,"feature_type":"variation","end":140462939,"alleles":["C","G","T"],"seq_region_name":"7","id":"rs925937915","clinical_significance":[]},{"source":"dbSNP","start":140462943,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140462943,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs955380155"},{"strand":1,"feature_type":"variation","end":140462946,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462946,"source":"dbSNP","seq_region_name":"7","id":"rs1794664495","clinical_significance":[]},{"clinical_significance":[],"id":"rs1483098995","seq_region_name":"7","feature_type":"variation","strand":1,"end":140462948,"alleles":["ACA","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462946},{"seq_region_name":"7","id":"rs1794664617","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140462949,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462949,"source":"dbSNP"},{"source":"dbSNP","start":140462961,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140462961,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs987303568"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462963,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140462963,"seq_region_name":"7","id":"rs936102874","clinical_significance":[]},{"id":"rs1794666668","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140462965,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462965,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462970,"feature_type":"variation","strand":1,"end":140462970,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794666726"},{"clinical_significance":[],"id":"rs1053181055","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462971,"feature_type":"variation","strand":1,"end":140462971,"alleles":["C","A","G"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462974,"feature_type":"variation","strand":1,"end":140462974,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794666826"},{"id":"rs1794666929","seq_region_name":"7","clinical_significance":[],"start":140462975,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140462977,"alleles":["AAA","A","AAAA"],"strand":1,"feature_type":"variation"},{"start":140462977,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140462977,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs911338520","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794667070","feature_type":"variation","strand":1,"end":140462978,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462978},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140462980,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140462980,"clinical_significance":[],"seq_region_name":"7","id":"rs1794667114"},{"seq_region_name":"7","id":"rs891872805","clinical_significance":[],"start":140462983,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140462983,"strand":1,"feature_type":"variation"},{"end":140462984,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140462984,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1306286555"},{"clinical_significance":[],"id":"rs1014453668","seq_region_name":"7","source":"dbSNP","start":140462985,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140462985,"feature_type":"variation","strand":1},{"id":"rs190369199","seq_region_name":"7","clinical_significance":[],"start":140462986,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140462986,"strand":1,"feature_type":"variation"},{"alleles":["C","T"],"end":140462987,"strand":1,"feature_type":"variation","start":140462987,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1335044114","clinical_significance":[]},{"id":"rs1476528168","seq_region_name":"7","clinical_significance":[],"start":140462988,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140462988,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs906146138","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140462990,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140462990,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585474852","source":"dbSNP","start":140462993,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140462993,"alleles":["C","A","T"],"feature_type":"variation","strand":1},{"end":140462994,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140462994,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794667721"},{"end":140462998,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140462998,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794667821","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463001,"source":"dbSNP","strand":1,"feature_type":"variation","end":140463001,"alleles":["T","C"],"seq_region_name":"7","id":"rs1378122951","clinical_significance":[]},{"end":140463003,"alleles":["T","TT"],"strand":1,"feature_type":"variation","start":140463003,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1298547136","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140463004,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140463004,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794668153"},{"clinical_significance":[],"seq_region_name":"7","id":"rs182005789","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463009,"feature_type":"variation","strand":1,"end":140463009,"alleles":["C","T"]},{"clinical_significance":[],"id":"rs183577062","seq_region_name":"7","source":"dbSNP","start":140463014,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140463014,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130285872","alleles":["T","C"],"end":140463015,"feature_type":"variation","strand":1,"source":"dbSNP","start":140463015,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140463016,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140463016,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs1017011678","seq_region_name":"7","clinical_significance":[]},{"start":140463017,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140463017,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs772980351","clinical_significance":[]},{"clinical_significance":[],"id":"rs1794668447","seq_region_name":"7","end":140463019,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140463019,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463025,"source":"dbSNP","strand":1,"feature_type":"variation","end":140463025,"alleles":["C","T"],"seq_region_name":"7","id":"rs1794668501","clinical_significance":[]},{"end":140463026,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140463026,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1794668557","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463028,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140463028,"id":"rs1794668601","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794668655","clinical_significance":[],"alleles":["G","A"],"end":140463029,"strand":1,"feature_type":"variation","start":140463029,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1462076411","end":140463030,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140463030,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1420139426","clinical_significance":[],"alleles":["A","G"],"end":140463031,"strand":1,"feature_type":"variation","start":140463031,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140463034,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463034,"source":"dbSNP","seq_region_name":"7","id":"rs2130286021","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794668856","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140463035,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463035,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463038,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140463038,"clinical_significance":[],"seq_region_name":"7","id":"rs1585474917"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794668972","end":140463039,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140463039,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794669044","source":"dbSNP","start":140463042,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TT","-"],"end":140463043,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140463043,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140463043,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1358290780"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794669161","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463044,"feature_type":"variation","strand":1,"end":140463044,"alleles":["G","A","T"]},{"start":140463046,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140463046,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1563090467","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463047,"feature_type":"variation","strand":1,"end":140463047,"alleles":["G","A"],"clinical_significance":[],"id":"rs1794669287","seq_region_name":"7"},{"id":"rs554597446","seq_region_name":"7","clinical_significance":[],"end":140463049,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140463049,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1423470384","seq_region_name":"7","end":140463050,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140463050,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs994227268","end":140463053,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140463053,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130286197","source":"dbSNP","start":140463055,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140463055,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463057,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140463057,"clinical_significance":[],"seq_region_name":"7","id":"rs1025374711"},{"seq_region_name":"7","id":"rs1179382385","clinical_significance":[],"end":140463058,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140463058,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463062,"source":"dbSNP","strand":1,"feature_type":"variation","end":140463062,"alleles":["C","G"],"seq_region_name":"7","id":"rs955124233","clinical_significance":[]},{"clinical_significance":[],"id":"rs946289947","seq_region_name":"7","alleles":["CC","C"],"end":140463063,"feature_type":"variation","strand":1,"source":"dbSNP","start":140463062,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs140400480","clinical_significance":[],"start":140463068,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140463068,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140463071,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463071,"clinical_significance":[],"id":"rs1270938134","seq_region_name":"7"},{"source":"dbSNP","start":140463074,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140463074,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1274538799"},{"id":"rs1794669858","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463076,"source":"dbSNP","strand":1,"feature_type":"variation","end":140463076,"alleles":["A","G"]},{"id":"rs868829633","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463078,"source":"dbSNP","strand":1,"feature_type":"variation","end":140463078,"alleles":["G","A","T"]},{"id":"rs939056476","seq_region_name":"7","clinical_significance":[],"end":140463079,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140463079,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs2130286361","seq_region_name":"7","clinical_significance":[],"end":140463086,"alleles":["TGAAACC","-"],"strand":1,"feature_type":"variation","start":140463080,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1794670054","clinical_significance":[],"start":140463084,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140463090,"alleles":["ACCACCA","ACCA"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1056514465","clinical_significance":[],"start":140463085,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140463085,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"end":140463088,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140463088,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs188261401"},{"seq_region_name":"7","id":"rs1277640357","clinical_significance":[],"start":140463090,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140463090,"strand":1,"feature_type":"variation"},{"alleles":["C","G"],"end":140463092,"feature_type":"variation","strand":1,"source":"dbSNP","start":140463092,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1374539849","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140463095,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463095,"clinical_significance":[],"seq_region_name":"7","id":"rs180904549"},{"alleles":["A","G"],"end":140463098,"strand":1,"feature_type":"variation","start":140463098,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs894937072","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140463099,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463099,"source":"dbSNP","seq_region_name":"7","id":"rs1794670515","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs577083606","feature_type":"variation","strand":1,"end":140463101,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463101},{"source":"dbSNP","start":140463103,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A","C"],"end":140463103,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1396693248"},{"id":"rs1291877223","seq_region_name":"7","clinical_significance":[],"alleles":["A","C"],"end":140463106,"strand":1,"feature_type":"variation","start":140463106,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140463107,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463107,"clinical_significance":[],"seq_region_name":"7","id":"rs1011943281"},{"id":"rs1346086445","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140463109,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463109,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140463112,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463112,"source":"dbSNP","seq_region_name":"7","id":"rs1794670782","clinical_significance":[]},{"start":140463112,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["CTC","C"],"end":140463114,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1442167303","clinical_significance":[]},{"seq_region_name":"7","id":"rs1016729947","clinical_significance":[],"end":140463113,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","start":140463113,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794670958","end":140463119,"alleles":["TCTT","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140463116,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1794671016","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140463118,"strand":1,"feature_type":"variation","start":140463118,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463125,"source":"dbSNP","strand":1,"feature_type":"variation","end":140463125,"alleles":["T","C"],"seq_region_name":"7","id":"rs1794671064","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463127,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140463127,"clinical_significance":[],"seq_region_name":"7","id":"rs1794671121"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1438283549","source":"dbSNP","start":140463138,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140463138,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1216096366","seq_region_name":"7","source":"dbSNP","start":140463140,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140463140,"feature_type":"variation","strand":1},{"start":140463141,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140463141,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs866154099","clinical_significance":[]},{"source":"dbSNP","start":140463142,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140463142,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794671365"},{"id":"rs544446265","seq_region_name":"7","clinical_significance":[],"start":140463146,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140463146,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463147,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140463147,"id":"rs1264948964","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140463151,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140463151,"alleles":["A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1455970846"},{"seq_region_name":"7","id":"rs1268823509","clinical_significance":[],"start":140463155,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140463155,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs936044701","feature_type":"variation","strand":1,"end":140463159,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463159},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794671709","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463167,"feature_type":"variation","strand":1,"end":140463167,"alleles":["T","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1053089692","alleles":["T","C"],"end":140463173,"feature_type":"variation","strand":1,"source":"dbSNP","start":140463173,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1794671791","clinical_significance":[],"end":140463174,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140463174,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140463178,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463178,"clinical_significance":[],"seq_region_name":"7","id":"rs1794671860"},{"alleles":["C","T"],"end":140463179,"feature_type":"variation","strand":1,"source":"dbSNP","start":140463179,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1207621802","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1794671932","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["CC","C"],"end":140463180,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463179,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794671979","end":140463180,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140463180,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["A","T"],"end":140463181,"strand":1,"feature_type":"variation","start":140463181,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794672034","clinical_significance":[]},{"alleles":["C","G"],"end":140463182,"feature_type":"variation","strand":1,"source":"dbSNP","start":140463182,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1794672108","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1487936017","feature_type":"variation","strand":1,"alleles":["AAAAA","AAAA"],"end":140463187,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463183},{"seq_region_name":"7","id":"rs1585475138","clinical_significance":[],"strand":1,"feature_type":"variation","end":140463194,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463194,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs913358229","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463196,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140463196},{"clinical_significance":[],"seq_region_name":"7","id":"rs994511216","end":140463197,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140463197,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794672615","feature_type":"variation","strand":1,"end":140463199,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463199},{"feature_type":"variation","strand":1,"end":140463203,"alleles":["TTCT","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463200,"clinical_significance":[],"seq_region_name":"7","id":"rs1794672685"},{"seq_region_name":"7","id":"rs1794672777","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463202,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140463202},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794672843","source":"dbSNP","start":140463203,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TATA","TA"],"end":140463206,"feature_type":"variation","strand":1},{"id":"rs950103977","seq_region_name":"7","clinical_significance":[],"start":140463205,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140463205,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1308261102","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463206,"feature_type":"variation","strand":1,"end":140463206,"alleles":["A","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1045937553","feature_type":"variation","strand":1,"end":140463207,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463207},{"clinical_significance":[],"seq_region_name":"7","id":"rs562953548","alleles":["C","G"],"end":140463216,"feature_type":"variation","strand":1,"source":"dbSNP","start":140463216,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140463219,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140463219,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1429302866","seq_region_name":"7"},{"seq_region_name":"7","id":"rs905990519","clinical_significance":[],"alleles":["A","G"],"end":140463222,"strand":1,"feature_type":"variation","start":140463222,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["G","A"],"end":140463223,"strand":1,"feature_type":"variation","start":140463223,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1478968894","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1362896508","clinical_significance":[],"start":140463226,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140463226,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1002209332","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463233,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140463233},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463234,"source":"dbSNP","strand":1,"feature_type":"variation","end":140463234,"alleles":["A","C"],"seq_region_name":"7","id":"rs375318591","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463240,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140463240,"clinical_significance":[],"seq_region_name":"7","id":"rs1038587224"},{"end":140463244,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140463244,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs574915710","seq_region_name":"7"},{"alleles":["A","G"],"end":140463246,"strand":1,"feature_type":"variation","start":140463246,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794673749","clinical_significance":[]},{"end":140463250,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140463250,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs541852717"},{"source":"dbSNP","start":140463254,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140463254,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794673874"},{"alleles":["T","-"],"end":140463254,"strand":1,"feature_type":"variation","start":140463254,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs2130287224","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794673940","clinical_significance":[],"strand":1,"feature_type":"variation","end":140463258,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463258,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1360216942","clinical_significance":[],"start":140463258,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["CTCT","CT"],"end":140463261,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140463260,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["CTTTCACTTTCACT","CTTTCACT"],"end":140463273,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs778238146","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1174720039","clinical_significance":[],"alleles":["T","A"],"end":140463262,"strand":1,"feature_type":"variation","start":140463262,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1794674176","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140463263,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463263,"source":"dbSNP"},{"id":"rs186192286","seq_region_name":"7","clinical_significance":[],"alleles":["A","T"],"end":140463265,"strand":1,"feature_type":"variation","start":140463265,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463267,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140463267,"seq_region_name":"7","id":"rs890884680","clinical_significance":[]},{"source":"dbSNP","start":140463275,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140463275,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794674369"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463276,"feature_type":"variation","strand":1,"end":140463276,"alleles":["T","C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs964160763"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1261854080","alleles":["G","A","C"],"end":140463277,"feature_type":"variation","strand":1,"source":"dbSNP","start":140463277,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140463278,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AA","AAA"],"end":140463279,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1401122586"},{"end":140463279,"alleles":["A","AAGTGGGGA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140463279,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1487109872","seq_region_name":"7"},{"source":"dbSNP","start":140463280,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140463280,"alleles":["C","A","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs990200850"},{"seq_region_name":"7","id":"rs914748848","clinical_significance":[],"end":140463281,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140463281,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1347001769","end":140463282,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140463282,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1362763802","clinical_significance":[],"end":140463282,"alleles":["G","GGGGAAAG"],"strand":1,"feature_type":"variation","start":140463282,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463285,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140463285,"id":"rs1254231492","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463288,"feature_type":"variation","strand":1,"alleles":["AA","A"],"end":140463289,"clinical_significance":[],"id":"rs1794675065","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs773918282","end":140463290,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140463290,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463293,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140463293,"clinical_significance":[],"seq_region_name":"7","id":"rs1794675198"},{"source":"dbSNP","start":140463297,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140463297,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs551696452"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1398369981","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140463298,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463298},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140463299,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463299,"source":"dbSNP","seq_region_name":"7","id":"rs1794675373","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140463300,"alleles":["A","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463300,"clinical_significance":[],"seq_region_name":"7","id":"rs1794675419"},{"start":140463303,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140463303,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794675469","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1398322184","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463304,"feature_type":"variation","strand":1,"end":140463304,"alleles":["T","C"]},{"end":140463305,"alleles":["TA","-"],"strand":1,"feature_type":"variation","start":140463304,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1297822321","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463309,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140463309,"id":"rs1297673216","seq_region_name":"7","clinical_significance":[]},{"id":"rs946205910","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463312,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140463312},{"start":140463319,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140463319,"alleles":["T","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1417062111","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463321,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140463321,"clinical_significance":[],"id":"rs1400542546","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1172461779","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140463323,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463323,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1007893899","clinical_significance":[],"start":140463324,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140463324,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1346158347","source":"dbSNP","start":140463326,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140463326,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140463331,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463331,"source":"dbSNP","seq_region_name":"7","id":"rs10256074","clinical_significance":[]},{"start":140463335,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140463335,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs150394608","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140463338,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463338,"source":"dbSNP","id":"rs1794676207","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463339,"source":"dbSNP","strand":1,"feature_type":"variation","end":140463340,"alleles":["TT","TTT"],"id":"rs1273538182","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585475457","feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140463340,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463340},{"id":"rs1262074521","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463351,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140463351},{"alleles":["G","C"],"end":140463352,"feature_type":"variation","strand":1,"source":"dbSNP","start":140463352,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794676453"},{"clinical_significance":[],"id":"rs1794676513","seq_region_name":"7","alleles":["GGG","GG"],"end":140463354,"feature_type":"variation","strand":1,"source":"dbSNP","start":140463352,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs191438817","clinical_significance":[],"start":140463354,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140463354,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140463356,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463356,"source":"dbSNP","seq_region_name":"7","id":"rs1443883473","clinical_significance":[]},{"start":140463359,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","TT"],"end":140463359,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1253857683","clinical_significance":[]},{"seq_region_name":"7","id":"rs571695230","clinical_significance":[],"strand":1,"feature_type":"variation","end":140463360,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463360,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463364,"source":"dbSNP","strand":1,"feature_type":"variation","end":140463364,"alleles":["C","G"],"seq_region_name":"7","id":"rs1199740120","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794676837","clinical_significance":[],"start":140463366,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140463382,"alleles":["GCTCTATACAGTACAGC","GC"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs2130287957","seq_region_name":"7","feature_type":"variation","strand":1,"end":140463367,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463367},{"start":140463372,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140463372,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794676894","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130287978","feature_type":"variation","strand":1,"end":140463376,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463376},{"seq_region_name":"7","id":"rs1340008661","clinical_significance":[],"start":140463378,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140463378,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"start":140463379,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140463379,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585475501","clinical_significance":[]},{"clinical_significance":[],"id":"rs1794677049","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463382,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140463382},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463386,"source":"dbSNP","strand":1,"feature_type":"variation","end":140463386,"alleles":["C","T"],"seq_region_name":"7","id":"rs938929162","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1216918590","source":"dbSNP","start":140463390,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C","G"],"end":140463390,"feature_type":"variation","strand":1},{"id":"rs531774353","seq_region_name":"7","clinical_significance":[],"start":140463391,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140463391,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463392,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140463392,"clinical_significance":[],"seq_region_name":"7","id":"rs1794677299"},{"seq_region_name":"7","id":"rs1247295455","clinical_significance":[],"start":140463396,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140463396,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1224729561","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["CATC","CATCATC"],"end":140463399,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463396,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140463399,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463399,"source":"dbSNP","seq_region_name":"7","id":"rs1794677473","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794677539","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140463400,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463400,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1032284426","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140463403,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463403},{"alleles":["C","T"],"end":140463405,"feature_type":"variation","strand":1,"source":"dbSNP","start":140463405,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1333932911","seq_region_name":"7"},{"end":140463407,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140463407,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1392464367","clinical_significance":[]},{"seq_region_name":"7","id":"rs1399347130","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463409,"source":"dbSNP","strand":1,"feature_type":"variation","end":140463411,"alleles":["AGA","A"]},{"strand":1,"feature_type":"variation","end":140463412,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463412,"source":"dbSNP","seq_region_name":"7","id":"rs1585475573","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794677866","clinical_significance":[],"start":140463414,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TACATACA","TACA"],"end":140463421,"strand":1,"feature_type":"variation"},{"id":"rs1794677913","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140463416,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463416,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1794677956","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463418,"source":"dbSNP","strand":1,"feature_type":"variation","end":140463418,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs947808577","source":"dbSNP","start":140463420,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140463420,"alleles":["C","A","G","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1165149099","seq_region_name":"7","source":"dbSNP","start":140463427,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140463429,"alleles":["AAA","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1473579090","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463432,"feature_type":"variation","strand":1,"end":140463432,"alleles":["C","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463438,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140463438,"seq_region_name":"7","id":"rs1215349255","clinical_significance":[]},{"id":"rs1186649176","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140463443,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463443,"source":"dbSNP"},{"start":140463449,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G","T"],"end":140463449,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1269010085","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794678362","clinical_significance":[],"start":140463451,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140463451,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463452,"source":"dbSNP","strand":1,"feature_type":"variation","end":140463452,"alleles":["T","C"],"seq_region_name":"7","id":"rs747850766","clinical_significance":[]},{"source":"dbSNP","start":140463457,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["ATACCTGCA","A"],"end":140463465,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794678477"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140463459,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463459,"source":"dbSNP","seq_region_name":"7","id":"rs1196695634","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794678555","feature_type":"variation","strand":1,"alleles":["CC","C"],"end":140463461,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463460},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140463463,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463463,"clinical_significance":[],"id":"rs1794678631","seq_region_name":"7"},{"clinical_significance":[],"id":"rs749800438","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463464,"feature_type":"variation","strand":1,"alleles":["C","CC"],"end":140463464},{"start":140463464,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140463464,"alleles":["C","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130288421","clinical_significance":[]},{"seq_region_name":"7","id":"rs988844399","clinical_significance":[],"start":140463467,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140463467,"alleles":["G","A","C"],"strand":1,"feature_type":"variation"},{"id":"rs1457340612","seq_region_name":"7","clinical_significance":[],"start":140463476,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140463476,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"alleles":["A","G"],"end":140463482,"feature_type":"variation","strand":1,"source":"dbSNP","start":140463482,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1196099805","seq_region_name":"7"},{"start":140463483,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140463483,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794678919","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1211798466","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140463485,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463485},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463487,"feature_type":"variation","strand":1,"alleles":["G","-"],"end":140463487,"clinical_significance":[],"seq_region_name":"7","id":"rs1794679049"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140463489,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463489,"clinical_significance":[],"seq_region_name":"7","id":"rs1354579154"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463493,"source":"dbSNP","strand":1,"feature_type":"variation","end":140463493,"alleles":["A","G"],"seq_region_name":"7","id":"rs1246093077","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs994044004","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463494,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140463494},{"seq_region_name":"7","id":"rs181719032","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140463499,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463499,"source":"dbSNP"},{"clinical_significance":[],"id":"rs950113918","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140463500,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463500},{"feature_type":"variation","strand":1,"end":140463503,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463503,"clinical_significance":[],"seq_region_name":"7","id":"rs1025881348"},{"clinical_significance":[],"seq_region_name":"7","id":"rs796860766","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140463506,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463506},{"seq_region_name":"7","id":"rs1446738057","clinical_significance":[],"end":140463513,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140463513,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463514,"feature_type":"variation","strand":1,"end":140463514,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794679571"},{"alleles":["G","A"],"end":140463518,"feature_type":"variation","strand":1,"source":"dbSNP","start":140463518,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794679627"},{"seq_region_name":"7","id":"rs1794679678","clinical_significance":[],"end":140463522,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140463522,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463530,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140463530,"id":"rs1794679726","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140463532,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463532,"source":"dbSNP","seq_region_name":"7","id":"rs1160297136","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463534,"source":"dbSNP","strand":1,"feature_type":"variation","end":140463534,"alleles":["G","A"],"seq_region_name":"7","id":"rs891085856","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794679899","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463538,"feature_type":"variation","strand":1,"end":140463538,"alleles":["G","T"]},{"seq_region_name":"7","id":"rs1406727786","clinical_significance":[],"end":140463539,"alleles":["A","G","T"],"strand":1,"feature_type":"variation","start":140463539,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140463550,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140463550,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1794680018","seq_region_name":"7"},{"alleles":["A","T"],"end":140463551,"strand":1,"feature_type":"variation","start":140463551,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1388181904","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794680118","clinical_significance":[],"strand":1,"feature_type":"variation","end":140463554,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463554,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1008556739","seq_region_name":"7","end":140463562,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140463562,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140463573,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463573,"source":"dbSNP","seq_region_name":"7","id":"rs981500454","clinical_significance":[]},{"source":"dbSNP","start":140463574,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G","T"],"end":140463574,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1381971791"},{"clinical_significance":[],"id":"rs1794680348","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463574,"feature_type":"variation","strand":1,"alleles":["AGCAGCA","AGCA"],"end":140463580},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463575,"feature_type":"variation","strand":1,"end":140463575,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794680405"},{"clinical_significance":[],"seq_region_name":"7","id":"rs964002682","source":"dbSNP","start":140463576,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140463576,"alleles":["C","T"],"feature_type":"variation","strand":1},{"alleles":["G","A"],"end":140463578,"feature_type":"variation","strand":1,"source":"dbSNP","start":140463578,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794680516"},{"clinical_significance":[],"id":"rs1439019369","seq_region_name":"7","alleles":["C","T"],"end":140463579,"feature_type":"variation","strand":1,"source":"dbSNP","start":140463579,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["A","G"],"end":140463580,"feature_type":"variation","strand":1,"source":"dbSNP","start":140463580,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs990245007"},{"start":140463582,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140463582,"strand":1,"feature_type":"variation","id":"rs1223950311","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140463585,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463585,"source":"dbSNP","seq_region_name":"7","id":"rs1327765509","clinical_significance":[]},{"id":"rs1450054688","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463586,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140463586},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794680801","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463586,"feature_type":"variation","strand":1,"end":140463602,"alleles":["CCTTAGAAATCCAGCCC","CC"]},{"id":"rs1289499484","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140463589,"strand":1,"feature_type":"variation","start":140463589,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140463591,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140463591,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1205970705","clinical_significance":[]},{"source":"dbSNP","start":140463594,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140463594,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794680958"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1356252024","alleles":["C","T"],"end":140463597,"feature_type":"variation","strand":1,"source":"dbSNP","start":140463597,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1794681064","clinical_significance":[],"end":140463600,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140463600,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1284332321","clinical_significance":[],"strand":1,"feature_type":"variation","end":140463601,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463601,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794681181","end":140463604,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140463604,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140463605,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140463605,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1418105427"},{"clinical_significance":[],"id":"rs1794681326","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463606,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140463606},{"seq_region_name":"7","id":"rs117821902","clinical_significance":[],"alleles":["T","A","C","G"],"end":140463607,"strand":1,"feature_type":"variation","start":140463607,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs937550334","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140463608,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463608},{"clinical_significance":[],"seq_region_name":"7","id":"rs117152518","alleles":["A","G","T"],"end":140463610,"feature_type":"variation","strand":1,"source":"dbSNP","start":140463610,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1321640251","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140463611,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463611,"source":"dbSNP"},{"source":"dbSNP","start":140463612,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140463612,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs898784869"},{"seq_region_name":"7","id":"rs566428878","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463613,"source":"dbSNP","strand":1,"feature_type":"variation","end":140463613,"alleles":["C","G","T"]},{"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140463614,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463614,"source":"dbSNP","seq_region_name":"7","id":"rs138147788","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794681992","source":"dbSNP","start":140463615,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140463615,"alleles":["G","A"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463618,"feature_type":"variation","strand":1,"end":140463618,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs149577943"},{"feature_type":"variation","strand":1,"end":140463619,"alleles":["C","A","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463619,"clinical_significance":[],"seq_region_name":"7","id":"rs1192973416"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1007946231","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463620,"feature_type":"variation","strand":1,"end":140463620,"alleles":["T","A","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130289310","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463620,"feature_type":"variation","strand":1,"end":140463633,"alleles":["TCACGCCTGTAATC","TC"]},{"source":"dbSNP","start":140463621,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140463621,"alleles":["C","A","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs991661094"},{"seq_region_name":"7","id":"rs1794682361","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463622,"source":"dbSNP","strand":1,"feature_type":"variation","end":140463622,"alleles":["A","G"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463623,"source":"dbSNP","strand":1,"feature_type":"variation","end":140463623,"alleles":["C","G","T"],"seq_region_name":"7","id":"rs538377050","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs899561317","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463624,"feature_type":"variation","strand":1,"end":140463624,"alleles":["G","A","C"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463625,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140463625,"seq_region_name":"7","id":"rs1281281279","clinical_significance":[]},{"source":"dbSNP","start":140463626,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140463626,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1218014031"},{"alleles":["G","A"],"end":140463628,"strand":1,"feature_type":"variation","start":140463628,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1207619938","clinical_significance":[]},{"end":140463629,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140463629,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1273743388","clinical_significance":[]},{"id":"rs1000744081","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463630,"source":"dbSNP","strand":1,"feature_type":"variation","end":140463630,"alleles":["A","G"]},{"id":"rs1794682826","seq_region_name":"7","clinical_significance":[],"start":140463632,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140463632,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1032581686","seq_region_name":"7","source":"dbSNP","start":140463633,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140463633,"feature_type":"variation","strand":1},{"alleles":["C","T"],"end":140463634,"feature_type":"variation","strand":1,"source":"dbSNP","start":140463634,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs956657127"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463635,"feature_type":"variation","strand":1,"end":140463635,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs538028747"},{"seq_region_name":"7","id":"rs1236168813","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140463636,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463636,"source":"dbSNP"},{"start":140463637,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140463637,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","id":"rs890922056","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130289551","clinical_significance":[],"end":140463639,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140463639,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs556442483","source":"dbSNP","start":140463640,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140463640,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463642,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140463642,"id":"rs375863587","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","C"],"end":140463643,"strand":1,"feature_type":"variation","start":140463643,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1794683399","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1171548079","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140463644,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463644,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463646,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140463646,"seq_region_name":"7","id":"rs1011606070","clinical_significance":[]},{"clinical_significance":[],"id":"rs988015841","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140463648,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463648},{"clinical_significance":[],"seq_region_name":"7","id":"rs574547567","source":"dbSNP","start":140463650,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140463650,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs542265519","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463651,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140463651},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463652,"source":"dbSNP","strand":1,"feature_type":"variation","end":140463652,"alleles":["A","G"],"seq_region_name":"7","id":"rs369979344","clinical_significance":[]},{"clinical_significance":[],"id":"rs1794683779","seq_region_name":"7","end":140463653,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140463653,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1794683836","seq_region_name":"7","feature_type":"variation","strand":1,"end":140463655,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463655},{"start":140463656,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140463656,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","id":"rs578156577","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1021630650","alleles":["G","A","C"],"end":140463657,"feature_type":"variation","strand":1,"source":"dbSNP","start":140463657,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["G","A","C"],"end":140463658,"strand":1,"feature_type":"variation","start":140463658,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs927441260","clinical_significance":[]},{"source":"dbSNP","start":140463659,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140463659,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs999310972"},{"seq_region_name":"7","id":"rs369963812","clinical_significance":[],"alleles":["C","A","G","T"],"end":140463660,"strand":1,"feature_type":"variation","start":140463660,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1794684330","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463661,"source":"dbSNP","strand":1,"feature_type":"variation","end":140463660,"alleles":["-","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs991715053","feature_type":"variation","strand":1,"end":140463661,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463661},{"clinical_significance":[],"seq_region_name":"7","id":"rs916193924","source":"dbSNP","start":140463662,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140463662,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140463663,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140463663,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs963579383"},{"end":140463664,"alleles":["T","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140463664,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs973748933","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs373393062","source":"dbSNP","start":140463665,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140463665,"alleles":["C","T"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140463666,"alleles":["-","GGAGATCGCCCAT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463667,"source":"dbSNP","seq_region_name":"7","id":"rs1794684716","clinical_significance":[]},{"clinical_significance":[],"id":"rs929752032","seq_region_name":"7","feature_type":"variation","strand":1,"end":140463667,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463667},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463668,"feature_type":"variation","strand":1,"end":140463667,"alleles":["-","CT"],"clinical_significance":[],"id":"rs1794684840","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs187147657","source":"dbSNP","start":140463668,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140463668,"alleles":["A","C","G","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1416390122","clinical_significance":[],"start":140463670,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C","T"],"end":140463670,"strand":1,"feature_type":"variation"},{"id":"rs1239367578","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463671,"source":"dbSNP","strand":1,"feature_type":"variation","end":140463671,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs112279242","clinical_significance":[],"alleles":["T","C"],"end":140463672,"strand":1,"feature_type":"variation","start":140463672,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs768799927","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463673,"source":"dbSNP","strand":1,"feature_type":"variation","end":140463673,"alleles":["C","G","T"]},{"clinical_significance":[],"id":"rs920049732","seq_region_name":"7","source":"dbSNP","start":140463674,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140463674,"feature_type":"variation","strand":1},{"id":"rs1794685312","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463675,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GGAGATGGAGA","GGAGA"],"end":140463685},{"clinical_significance":[],"seq_region_name":"7","id":"rs368871661","feature_type":"variation","strand":1,"end":140463676,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463676},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794685441","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463677,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140463677},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463678,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140463678,"clinical_significance":[],"seq_region_name":"7","id":"rs1047276868"},{"feature_type":"variation","strand":1,"end":140463679,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463679,"clinical_significance":[],"seq_region_name":"7","id":"rs564431902"},{"clinical_significance":[],"seq_region_name":"7","id":"rs774234396","alleles":["T","C","G"],"end":140463680,"feature_type":"variation","strand":1,"source":"dbSNP","start":140463680,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs10238372","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463681,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C","T"],"end":140463681},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463682,"source":"dbSNP","strand":1,"feature_type":"variation","end":140463682,"alleles":["G","A","T"],"seq_region_name":"7","id":"rs1039772998","clinical_significance":[]},{"end":140463684,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140463684,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1264365194","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794686015","feature_type":"variation","strand":1,"end":140463685,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463685},{"seq_region_name":"7","id":"rs2130290206","clinical_significance":[],"start":140463686,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140463686,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs903143235","source":"dbSNP","start":140463688,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140463688,"alleles":["A","G"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140463689,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140463689,"alleles":["T","A","C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs899614484"},{"seq_region_name":"7","id":"rs1381354985","clinical_significance":[],"start":140463690,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140463690,"alleles":["C","G","T"],"strand":1,"feature_type":"variation"},{"start":140463691,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140463691,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs562268978","clinical_significance":[]},{"seq_region_name":"7","id":"rs1053628423","clinical_significance":[],"start":140463692,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C","G"],"end":140463692,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463693,"source":"dbSNP","strand":1,"feature_type":"variation","end":140463693,"alleles":["G","A","T"],"seq_region_name":"7","id":"rs540795508","clinical_significance":[]},{"seq_region_name":"7","id":"rs1266892534","clinical_significance":[],"strand":1,"feature_type":"variation","end":140463694,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463694,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463695,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140463695,"clinical_significance":[],"seq_region_name":"7","id":"rs1009499417"},{"alleles":["T","C"],"end":140463696,"strand":1,"feature_type":"variation","start":140463696,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs572355158","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs566471740","source":"dbSNP","start":140463697,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140463697,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1002910241","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463698,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140463698},{"feature_type":"variation","strand":1,"end":140463699,"alleles":["C","A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463699,"clinical_significance":[],"seq_region_name":"7","id":"rs1308578683"},{"source":"dbSNP","start":140463700,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140463700,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1387472446"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463701,"feature_type":"variation","strand":1,"end":140463701,"alleles":["C","A","G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs533753974"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463702,"feature_type":"variation","strand":1,"alleles":["G","A","C","T"],"end":140463702,"clinical_significance":[],"seq_region_name":"7","id":"rs10238384"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463703,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140463703,"seq_region_name":"7","id":"rs1160889795","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1465560509","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140463704,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463704},{"start":140463710,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140463710,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794687330","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs373225924","feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140463711,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463711},{"clinical_significance":[],"id":"rs1563091003","seq_region_name":"7","alleles":["T","-"],"end":140463711,"feature_type":"variation","strand":1,"source":"dbSNP","start":140463711,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["TCGT","-"],"end":140463714,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463711,"clinical_significance":[],"seq_region_name":"7","id":"rs1794687650"},{"start":140463712,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140463712,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs920119561","clinical_significance":[]},{"seq_region_name":"7","id":"rs573282745","clinical_significance":[],"strand":1,"feature_type":"variation","end":140463713,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463713,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1794687924","clinical_significance":[],"strand":1,"feature_type":"variation","end":140463714,"alleles":["GT","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463713,"source":"dbSNP"},{"start":140463714,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140463714,"alleles":["T","A"],"strand":1,"feature_type":"variation","id":"rs1794688005","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794688100","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463715,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140463715},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794688188","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463716,"feature_type":"variation","strand":1,"alleles":["-","CA"],"end":140463715},{"seq_region_name":"7","id":"rs1189037829","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140463716,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463716,"source":"dbSNP"},{"end":140463718,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140463718,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs570753412","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140463720,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463720,"clinical_significance":[],"seq_region_name":"7","id":"rs975276170"},{"seq_region_name":"7","id":"rs190982135","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463722,"source":"dbSNP","strand":1,"feature_type":"variation","end":140463722,"alleles":["A","G"]},{"id":"rs1263623337","seq_region_name":"7","clinical_significance":[],"start":140463722,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140463726,"alleles":["AAAAA","AAAA","AAAAAA"],"strand":1,"feature_type":"variation"},{"alleles":["C","A","T"],"end":140463729,"strand":1,"feature_type":"variation","start":140463729,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1260020237","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs762023333","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463730,"source":"dbSNP","strand":1,"feature_type":"variation","end":140463735,"alleles":["AAAAAA","AAAAAAA"]},{"seq_region_name":"7","id":"rs912854498","clinical_significance":[],"strand":1,"feature_type":"variation","end":140463731,"alleles":["A","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463731,"source":"dbSNP"},{"start":140463733,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140463733,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1275739715","clinical_significance":[]},{"end":140463734,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140463734,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794689259"},{"alleles":["A","T"],"end":140463735,"feature_type":"variation","strand":1,"source":"dbSNP","start":140463735,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1233916339"},{"source":"dbSNP","start":140463738,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140463738,"alleles":["A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1794689431","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1794689513","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463740,"feature_type":"variation","strand":1,"end":140463740,"alleles":["C","A"]},{"seq_region_name":"7","id":"rs2130290798","clinical_significance":[],"end":140463741,"alleles":["CC","CCC"],"strand":1,"feature_type":"variation","start":140463740,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140463741,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140463741,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs767719339"},{"clinical_significance":[],"seq_region_name":"7","id":"rs544342923","source":"dbSNP","start":140463742,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140463742,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs920889307","clinical_significance":[],"start":140463744,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140463744,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs936450247","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463745,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140463745},{"strand":1,"feature_type":"variation","end":140463746,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463746,"source":"dbSNP","seq_region_name":"7","id":"rs1482133196","clinical_significance":[]},{"seq_region_name":"7","id":"rs562436610","clinical_significance":[],"start":140463747,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140463747,"alleles":["T","A","C"],"strand":1,"feature_type":"variation"},{"start":140463748,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140463748,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1360315937","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463750,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140463750,"clinical_significance":[],"seq_region_name":"7","id":"rs1794690306"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140463751,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463751,"source":"dbSNP","seq_region_name":"7","id":"rs1794690355","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs892205436","source":"dbSNP","start":140463753,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140463753,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463754,"feature_type":"variation","strand":1,"end":140463754,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs112023355"},{"start":140463755,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140463755,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs554225501","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585476473","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140463756,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463756,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs572491041","end":140463757,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140463757,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1195423285","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140463758,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463758,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["CCTGTAGTCCCA","-"],"end":140463770,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463759,"source":"dbSNP","id":"rs1012947737","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140463760,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140463760,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs545792798"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1002493915","alleles":["T","C"],"end":140463761,"feature_type":"variation","strand":1,"source":"dbSNP","start":140463761,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs552760910","alleles":["G","A"],"end":140463762,"feature_type":"variation","strand":1,"source":"dbSNP","start":140463762,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463763,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140463763,"clinical_significance":[],"seq_region_name":"7","id":"rs1023098932"},{"clinical_significance":[],"seq_region_name":"7","id":"rs576038370","source":"dbSNP","start":140463765,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140463765,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140463765,"alleles":["G","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463765,"clinical_significance":[],"seq_region_name":"7","id":"rs1196023393"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463766,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140463766,"seq_region_name":"7","id":"rs1477789119","clinical_significance":[]},{"source":"dbSNP","start":140463767,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140463767,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1794691356","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1280285988","clinical_significance":[],"start":140463771,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140463771,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1217071693","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463772,"feature_type":"variation","strand":1,"end":140463772,"alleles":["C","G","T"]},{"start":140463773,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140463773,"alleles":["T","C","G"],"strand":1,"feature_type":"variation","id":"rs995120836","seq_region_name":"7","clinical_significance":[]},{"end":140463774,"alleles":["A","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140463774,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs543675036"},{"end":140463775,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140463775,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585476565","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794691741","end":140463776,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140463776,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1398300292","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140463777,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463777},{"clinical_significance":[],"seq_region_name":"7","id":"rs1026956458","alleles":["G","A","C"],"end":140463778,"feature_type":"variation","strand":1,"source":"dbSNP","start":140463778,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140463778,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140463780,"alleles":["GGG","GG"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1400741473","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794691957","end":140463779,"alleles":["-","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140463780,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1468784587","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140463782,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463782,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794692082","end":140463788,"alleles":["G","C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140463788,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140463789,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140463789,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794692144","clinical_significance":[]},{"source":"dbSNP","start":140463789,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140463795,"alleles":["GGAGGAG","GGAG"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794692202"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463790,"feature_type":"variation","strand":1,"alleles":["G","A","C","T"],"end":140463790,"clinical_significance":[],"seq_region_name":"7","id":"rs376539828"},{"start":140463791,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140463791,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794692364","clinical_significance":[]},{"alleles":["A","C","G"],"end":140463794,"feature_type":"variation","strand":1,"source":"dbSNP","start":140463794,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794692418"},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140463795,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463795,"clinical_significance":[],"seq_region_name":"7","id":"rs1302611158"},{"seq_region_name":"7","id":"rs1425459190","clinical_significance":[],"end":140463798,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140463798,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794692590","alleles":["G","A"],"end":140463799,"feature_type":"variation","strand":1,"source":"dbSNP","start":140463799,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1019267781","clinical_significance":[],"alleles":["G","A"],"end":140463800,"strand":1,"feature_type":"variation","start":140463800,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140463801,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","G","T"],"end":140463801,"strand":1,"feature_type":"variation","id":"rs995507456","seq_region_name":"7","clinical_significance":[]},{"start":140463802,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140463801,"alleles":["-","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs35523693","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1027508657","source":"dbSNP","start":140463802,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140463802,"feature_type":"variation","strand":1},{"end":140463803,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140463803,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1295812113","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463804,"source":"dbSNP","strand":1,"feature_type":"variation","end":140463804,"alleles":["G","T"],"seq_region_name":"7","id":"rs147514770","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463806,"source":"dbSNP","strand":1,"feature_type":"variation","end":140463806,"alleles":["A","C","G"],"seq_region_name":"7","id":"rs1247500790","clinical_significance":[]},{"source":"dbSNP","start":140463807,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140463808,"alleles":["CC","CCC"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1219776200"},{"start":140463808,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140463808,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585476697","clinical_significance":[]},{"start":140463809,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C","G"],"end":140463809,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs370877096","clinical_significance":[]},{"start":140463810,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140463810,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs912695545","clinical_significance":[]},{"end":140463813,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140463813,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1310348494","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1332864503","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463814,"source":"dbSNP","strand":1,"feature_type":"variation","end":140463814,"alleles":["G","A"]},{"end":140463815,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140463815,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794693619"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463816,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140463816,"clinical_significance":[],"seq_region_name":"7","id":"rs965603446"},{"source":"dbSNP","start":140463817,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140463817,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs976044902"},{"clinical_significance":[],"id":"rs2130291677","seq_region_name":"7","feature_type":"variation","strand":1,"end":140463818,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463818},{"seq_region_name":"7","id":"rs947175186","clinical_significance":[],"start":140463819,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140463819,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"id":"rs1794693831","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140463820,"strand":1,"feature_type":"variation","start":140463820,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["C","A","G"],"end":140463824,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463824,"source":"dbSNP","seq_region_name":"7","id":"rs920950527","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463826,"feature_type":"variation","strand":1,"end":140463826,"alleles":["A","G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1182843345"},{"seq_region_name":"7","id":"rs1440301644","clinical_significance":[],"start":140463829,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["GAGAGAG","GAGAG"],"end":140463835,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463830,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140463830,"id":"rs1240096601","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1218999763","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463831,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140463831},{"alleles":["A","-"],"end":140463832,"strand":1,"feature_type":"variation","start":140463832,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1794694205","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140463833,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140463833,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1437439569"},{"strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140463834,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463834,"source":"dbSNP","seq_region_name":"7","id":"rs1290795686","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140463834,"alleles":["A","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463834,"clinical_significance":[],"seq_region_name":"7","id":"rs1794694358"},{"start":140463835,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140463835,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs2130291860","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463836,"source":"dbSNP","strand":1,"feature_type":"variation","end":140463836,"alleles":["C","G"],"seq_region_name":"7","id":"rs2130291876","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140463837,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463837,"clinical_significance":[],"seq_region_name":"7","id":"rs1794694416"},{"source":"dbSNP","start":140463838,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140463838,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1354603411"},{"seq_region_name":"7","id":"rs1291518758","clinical_significance":[],"end":140463841,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140463841,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140463843,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140463843,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs560184072","clinical_significance":[]},{"end":140463847,"alleles":["CGCGC","CGC"],"strand":1,"feature_type":"variation","start":140463843,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794694629","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1485561727","alleles":["G","A"],"end":140463844,"feature_type":"variation","strand":1,"source":"dbSNP","start":140463844,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140463845,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140463845,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs527429894","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","A"],"end":140463846,"feature_type":"variation","strand":1,"source":"dbSNP","start":140463846,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs936361105"},{"seq_region_name":"7","id":"rs1794694888","clinical_significance":[],"start":140463849,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140463849,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140463851,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463851,"source":"dbSNP","seq_region_name":"7","id":"rs1794694960","clinical_significance":[]},{"id":"rs1053436707","seq_region_name":"7","clinical_significance":[],"start":140463853,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140463853,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140463854,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140463854,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1585476863","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140463855,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463855,"source":"dbSNP","seq_region_name":"7","id":"rs1270155461","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794695376","clinical_significance":[],"alleles":["C","CC"],"end":140463855,"strand":1,"feature_type":"variation","start":140463855,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["CCA","CCACCA"],"end":140463859,"strand":1,"feature_type":"variation","start":140463857,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1794695456","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1794695533","seq_region_name":"7","source":"dbSNP","start":140463858,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140463858,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1794695610","clinical_significance":[],"strand":1,"feature_type":"variation","end":140463860,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463860,"source":"dbSNP"},{"alleles":["T","C"],"end":140463863,"feature_type":"variation","strand":1,"source":"dbSNP","start":140463863,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794695690"},{"feature_type":"variation","strand":1,"end":140463864,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463864,"clinical_significance":[],"seq_region_name":"7","id":"rs1323764308"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140463865,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463865,"clinical_significance":[],"seq_region_name":"7","id":"rs1431929742"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463866,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140463866,"id":"rs1794695974","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463867,"source":"dbSNP","strand":1,"feature_type":"variation","end":140463867,"alleles":["C","T"],"seq_region_name":"7","id":"rs913689900","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140463868,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463868,"clinical_significance":[],"id":"rs868768103","seq_region_name":"7"},{"start":140463870,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140463870,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1162766826","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1420198853","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463872,"feature_type":"variation","strand":1,"end":140463872,"alleles":["G","C"]},{"seq_region_name":"7","id":"rs1794696468","clinical_significance":[],"start":140463874,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140463874,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["C","CC"],"end":140463875,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463875,"source":"dbSNP","seq_region_name":"7","id":"rs1044436823","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1046268979","feature_type":"variation","strand":1,"end":140463876,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463876},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463878,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140463878,"seq_region_name":"7","id":"rs1794696678","clinical_significance":[]},{"clinical_significance":[],"id":"rs1794696776","seq_region_name":"7","alleles":["T","G"],"end":140463881,"feature_type":"variation","strand":1,"source":"dbSNP","start":140463881,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463884,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140463884,"seq_region_name":"7","id":"rs1794696863","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794696951","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["AT","ATAT"],"end":140463885,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463884,"source":"dbSNP"},{"clinical_significance":[],"id":"rs183512341","seq_region_name":"7","source":"dbSNP","start":140463885,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A","C"],"end":140463885,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1156401957","seq_region_name":"7","feature_type":"variation","strand":1,"end":140463886,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463886},{"alleles":["C","A"],"end":140463888,"strand":1,"feature_type":"variation","start":140463888,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1201198296","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140463889,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140463889,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs187968634"},{"end":140463898,"alleles":["AAAAAAAAAA","AAAAAAAAA","AAAAAAAAAAA","AAAAAAAAAAAA"],"strand":1,"feature_type":"variation","start":140463889,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1268624733","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794697603","clinical_significance":[],"end":140463892,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140463892,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1794697675","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463893,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140463893},{"seq_region_name":"7","id":"rs995445400","clinical_significance":[],"end":140463894,"alleles":["A","C","T"],"strand":1,"feature_type":"variation","start":140463894,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463895,"feature_type":"variation","strand":1,"end":140463895,"alleles":["A","G"],"clinical_significance":[],"id":"rs1284441247","seq_region_name":"7"},{"id":"rs1223746665","seq_region_name":"7","clinical_significance":[],"start":140463899,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140463899,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140463904,"alleles":["AAAAA","AA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463900,"source":"dbSNP","seq_region_name":"7","id":"rs1794698069","clinical_significance":[]},{"clinical_significance":[],"id":"rs1349257143","seq_region_name":"7","feature_type":"variation","strand":1,"end":140463902,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463902},{"source":"dbSNP","start":140463904,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140463904,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1274943354"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1026478099","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463905,"feature_type":"variation","strand":1,"end":140463905,"alleles":["G","T"]},{"alleles":["C","A"],"end":140463910,"feature_type":"variation","strand":1,"source":"dbSNP","start":140463910,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs189704478"},{"source":"dbSNP","start":140463913,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140463913,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1055480344"},{"feature_type":"variation","strand":1,"end":140463914,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463914,"clinical_significance":[],"seq_region_name":"7","id":"rs1794698637"},{"alleles":["CCC","CC"],"end":140463916,"feature_type":"variation","strand":1,"source":"dbSNP","start":140463914,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1302279888","seq_region_name":"7"},{"clinical_significance":[],"id":"rs899064807","seq_region_name":"7","end":140463916,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140463916,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1563091215","clinical_significance":[],"end":140463919,"alleles":["AAA","AAAAA"],"strand":1,"feature_type":"variation","start":140463917,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140463921,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140463921,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1400330457","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463922,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140463922,"clinical_significance":[],"seq_region_name":"7","id":"rs1794698998"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140463936,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463936,"source":"dbSNP","seq_region_name":"7","id":"rs1794699071","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463939,"feature_type":"variation","strand":1,"alleles":["TTTTGTTTTGTTTT","TTTTGTTTT"],"end":140463952,"clinical_significance":[],"id":"rs886722953","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1009115107","clinical_significance":[],"start":140463943,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140463943,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140463944,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140463944,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794699348"},{"start":140463949,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140463949,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1386082876","clinical_significance":[]},{"id":"rs1794699525","seq_region_name":"7","clinical_significance":[],"start":140463949,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140463954,"alleles":["TTTTTT","TTTTT","TTTTTTT"],"strand":1,"feature_type":"variation"},{"id":"rs1309733498","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463953,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140463953},{"start":140463955,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140463955,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794699742","clinical_significance":[]},{"alleles":["ACA","A"],"end":140463960,"feature_type":"variation","strand":1,"source":"dbSNP","start":140463958,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1416331394"},{"seq_region_name":"7","id":"rs1174461237","clinical_significance":[],"alleles":["T","C"],"end":140463962,"strand":1,"feature_type":"variation","start":140463962,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1794700012","seq_region_name":"7","feature_type":"variation","strand":1,"end":140463963,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463963},{"id":"rs1477145985","seq_region_name":"7","clinical_significance":[],"start":140463964,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140463975,"alleles":["TCACTCTGTCAC","TCAC"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140463965,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463965,"clinical_significance":[],"id":"rs1585477061","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140463967,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463967,"clinical_significance":[],"seq_region_name":"7","id":"rs1794700291"},{"feature_type":"variation","strand":1,"alleles":["CTCT","CT"],"end":140463970,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463967,"clinical_significance":[],"seq_region_name":"7","id":"rs1428917868"},{"seq_region_name":"7","id":"rs995953733","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463969,"source":"dbSNP","strand":1,"feature_type":"variation","end":140463969,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1286230057","end":140463970,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140463970,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1261490034","clinical_significance":[],"strand":1,"feature_type":"variation","end":140463971,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463971,"source":"dbSNP"},{"source":"dbSNP","start":140463973,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140463973,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1019291149"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1443559555","source":"dbSNP","start":140463979,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C","T"],"end":140463979,"feature_type":"variation","strand":1},{"alleles":["G","A"],"end":140463983,"feature_type":"variation","strand":1,"source":"dbSNP","start":140463983,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs965017325"},{"end":140463986,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140463986,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1378775480"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463987,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140463987,"clinical_significance":[],"id":"rs1794701020","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1794701095","clinical_significance":[],"start":140463988,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140463988,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463991,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140463991,"seq_region_name":"7","id":"rs1794701175","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs996612193","feature_type":"variation","strand":1,"end":140463992,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140463992},{"seq_region_name":"7","id":"rs1028105272","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140463993,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140463993},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794701375","end":140463994,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140463994,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1794701453","seq_region_name":"7","source":"dbSNP","start":140463995,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140463995,"alleles":["G","A"],"feature_type":"variation","strand":1},{"end":140463999,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","start":140463999,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs968439154","clinical_significance":[]},{"clinical_significance":[],"id":"rs1794701664","seq_region_name":"7","end":140464001,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140464001,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464002,"source":"dbSNP","strand":1,"feature_type":"variation","end":140464002,"alleles":["C","A"],"id":"rs1794701762","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs979042138","end":140464004,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140464004,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794701941","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140464007,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464007},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464009,"source":"dbSNP","strand":1,"feature_type":"variation","end":140464009,"alleles":["C","G","T"],"id":"rs924461627","seq_region_name":"7","clinical_significance":[]},{"start":140464010,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140464010,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794702122","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140464011,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464011,"source":"dbSNP","seq_region_name":"7","id":"rs1359714994","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585477150","source":"dbSNP","start":140464017,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140464017,"alleles":["A","C","T"],"feature_type":"variation","strand":1},{"start":140464019,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140464019,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794702401","clinical_significance":[]},{"start":140464020,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140464020,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585477154","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140464025,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464025,"source":"dbSNP","seq_region_name":"7","id":"rs1026934395","clinical_significance":[]},{"start":140464027,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140464027,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585477173","clinical_significance":[]},{"id":"rs1336223722","seq_region_name":"7","clinical_significance":[],"start":140464029,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140464029,"alleles":["T","TT"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585477183","end":140464029,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140464029,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464031,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140464031,"clinical_significance":[],"id":"rs956159744","seq_region_name":"7"},{"id":"rs1585477207","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140464033,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464033,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585477212","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464035,"feature_type":"variation","strand":1,"end":140464035,"alleles":["A","C"]},{"clinical_significance":[],"id":"rs2130293260","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140464037,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464037},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794703216","feature_type":"variation","strand":1,"end":140464038,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464038},{"alleles":["C","G"],"end":140464042,"strand":1,"feature_type":"variation","start":140464042,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794703298","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585477221","clinical_significance":[],"alleles":["A","C","G"],"end":140464043,"strand":1,"feature_type":"variation","start":140464043,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130293323","feature_type":"variation","strand":1,"alleles":["T","A"],"end":140464046,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464046},{"source":"dbSNP","start":140464047,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140464047,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1284193500"},{"end":140464048,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140464048,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1794703574","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794703652","end":140464052,"alleles":["GCTGG","GCTGGCTGG"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140464048,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140464051,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464051,"clinical_significance":[],"seq_region_name":"7","id":"rs1794703750"},{"source":"dbSNP","start":140464054,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140464054,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585477232"},{"alleles":["T","A","C"],"end":140464055,"strand":1,"feature_type":"variation","start":140464055,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs550019366","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1478934925","end":140464057,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140464057,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464060,"feature_type":"variation","strand":1,"end":140464060,"alleles":["G","C"],"clinical_significance":[],"id":"rs1417799885","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140464062,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464062,"source":"dbSNP","seq_region_name":"7","id":"rs375019294","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794704364","clinical_significance":[],"end":140464063,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140464063,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs535631154","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464064,"source":"dbSNP","strand":1,"feature_type":"variation","end":140464064,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1239670959","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464065,"feature_type":"variation","strand":1,"end":140464065,"alleles":["G","A"]},{"strand":1,"feature_type":"variation","end":140464078,"alleles":["CCACCAAGCC","CC"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464069,"source":"dbSNP","id":"rs1208676248","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464070,"source":"dbSNP","strand":1,"feature_type":"variation","end":140464070,"alleles":["C","G"],"seq_region_name":"7","id":"rs1794704693","clinical_significance":[]},{"start":140464072,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140464072,"alleles":["C","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794704769","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464077,"source":"dbSNP","strand":1,"feature_type":"variation","end":140464077,"alleles":["C","A","T"],"id":"rs1487792652","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140464081,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464081,"clinical_significance":[],"seq_region_name":"7","id":"rs1794704959"},{"seq_region_name":"7","id":"rs948696111","clinical_significance":[],"strand":1,"feature_type":"variation","end":140464084,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464084,"source":"dbSNP"},{"source":"dbSNP","start":140464089,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140464089,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794705114"},{"clinical_significance":[],"id":"rs1198867876","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464090,"feature_type":"variation","strand":1,"end":140464090,"alleles":["T","G"]},{"end":140464091,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140464091,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1193490476","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1044364017","source":"dbSNP","start":140464103,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140464103,"alleles":["G","A","C"],"feature_type":"variation","strand":1},{"alleles":["G","A"],"end":140464105,"feature_type":"variation","strand":1,"source":"dbSNP","start":140464105,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1239191492","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1379652513","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140464107,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464107,"source":"dbSNP"},{"seq_region_name":"7","id":"rs182327018","clinical_significance":[],"strand":1,"feature_type":"variation","end":140464108,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464108,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140464112,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464112,"clinical_significance":[],"id":"rs1585477324","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1794705554","seq_region_name":"7","source":"dbSNP","start":140464114,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140464114,"alleles":["T","A"],"feature_type":"variation","strand":1},{"alleles":["C","A"],"end":140464115,"strand":1,"feature_type":"variation","start":140464115,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1177139596","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140464119,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464119,"source":"dbSNP","id":"rs1794705668","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1019758565","clinical_significance":[],"end":140464120,"alleles":["T","C","G"],"strand":1,"feature_type":"variation","start":140464120,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140464124,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464124,"source":"dbSNP","seq_region_name":"7","id":"rs2130293767","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794705794","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140464129,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464129},{"start":140464129,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["GG","GGG"],"end":140464130,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1379366325","clinical_significance":[]},{"id":"rs1405592301","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140464130,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464130,"source":"dbSNP"},{"source":"dbSNP","start":140464133,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140464133,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794705974"},{"end":140464143,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140464143,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1794706031","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140464144,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464144,"source":"dbSNP","seq_region_name":"7","id":"rs1166300303","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140464150,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464150,"clinical_significance":[],"seq_region_name":"7","id":"rs187790402"},{"start":140464152,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140464152,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1467377642","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140464157,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464157,"source":"dbSNP","id":"rs1353024507","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1170030957","seq_region_name":"7","source":"dbSNP","start":140464162,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140464162,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1794706287","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140464165,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464165,"source":"dbSNP"},{"source":"dbSNP","start":140464167,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140464167,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1048367422"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464174,"feature_type":"variation","strand":1,"end":140464174,"alleles":["C","T"],"clinical_significance":[],"id":"rs1794706330","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464176,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140464176,"clinical_significance":[],"seq_region_name":"7","id":"rs1794706380"},{"source":"dbSNP","start":140464178,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140464178,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794706432"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464180,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140464180,"seq_region_name":"7","id":"rs565543713","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794706544","alleles":["G","A"],"end":140464183,"feature_type":"variation","strand":1,"source":"dbSNP","start":140464183,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140464186,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140464186,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1794706592","seq_region_name":"7"},{"id":"rs1794706652","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464187,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140464187},{"end":140464193,"alleles":["TT","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140464192,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794706713"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1331907530","source":"dbSNP","start":140464197,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140464197,"alleles":["G","A"],"feature_type":"variation","strand":1},{"id":"rs1029014637","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140464199,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464199,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140464200,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464200,"source":"dbSNP","id":"rs958311018","seq_region_name":"7","clinical_significance":[]},{"end":140464202,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140464202,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1178761073"},{"feature_type":"variation","strand":1,"end":140464205,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464205,"clinical_significance":[],"seq_region_name":"7","id":"rs1378984677"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464206,"feature_type":"variation","strand":1,"end":140464206,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs989561212"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794707099","alleles":["C","T"],"end":140464209,"feature_type":"variation","strand":1,"source":"dbSNP","start":140464209,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs913532983","clinical_significance":[],"start":140464210,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140464210,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs539507629","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464211,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140464211},{"source":"dbSNP","start":140464212,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140464212,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs376981805"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140464217,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464217,"clinical_significance":[],"seq_region_name":"7","id":"rs1585477467"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1372956339","source":"dbSNP","start":140464220,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140464220,"feature_type":"variation","strand":1},{"start":140464238,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140464238,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794707446","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794707532","clinical_significance":[],"start":140464240,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140464241,"alleles":["TT","TTTT"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1229036231","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464242,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140464242},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464256,"feature_type":"variation","strand":1,"end":140464256,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs754053215"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464258,"feature_type":"variation","strand":1,"end":140464258,"alleles":["G","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs557845481"},{"end":140464259,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140464259,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1243670200","clinical_significance":[]},{"seq_region_name":"7","id":"rs193002910","clinical_significance":[],"start":140464260,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140464260,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs754399214","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140464262,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464262},{"end":140464265,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140464265,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1794708173","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs996537254","feature_type":"variation","strand":1,"end":140464266,"alleles":["TT","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464265},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794708360","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464266,"feature_type":"variation","strand":1,"end":140464266,"alleles":["T","G"]},{"start":140464268,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140464268,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585477539","clinical_significance":[]},{"seq_region_name":"7","id":"rs1027990777","clinical_significance":[],"strand":1,"feature_type":"variation","end":140464269,"alleles":["T","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464269,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464271,"feature_type":"variation","strand":1,"end":140464271,"alleles":["G","C"],"clinical_significance":[],"id":"rs1585477551","seq_region_name":"7"},{"alleles":["T","C"],"end":140464273,"strand":1,"feature_type":"variation","start":140464273,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585477558","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1297752154","feature_type":"variation","strand":1,"end":140464274,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464274},{"alleles":["A","C"],"end":140464276,"strand":1,"feature_type":"variation","start":140464276,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1585477562","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1437473427","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140464277,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464277,"source":"dbSNP"},{"alleles":["C","T"],"end":140464278,"feature_type":"variation","strand":1,"source":"dbSNP","start":140464278,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1351970682","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464279,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CTATAATTCCAGCTA","CTA"],"end":140464293,"id":"rs1162136457","seq_region_name":"7","clinical_significance":[]},{"end":140464281,"alleles":["A","G","T"],"strand":1,"feature_type":"variation","start":140464281,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs968907802","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1161000196","feature_type":"variation","strand":1,"end":140464282,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464282},{"seq_region_name":"7","id":"rs765170748","clinical_significance":[],"start":140464284,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140464284,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"start":140464289,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140464289,"alleles":["A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794709499","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464294,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140464294,"seq_region_name":"7","id":"rs1794709581","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1247808699","alleles":["G","A","T"],"end":140464297,"feature_type":"variation","strand":1,"source":"dbSNP","start":140464297,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140464299,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464299,"clinical_significance":[],"seq_region_name":"7","id":"rs1794709764"},{"source":"dbSNP","start":140464301,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140464301,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1563091390","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464307,"source":"dbSNP","strand":1,"feature_type":"variation","end":140464307,"alleles":["G","C"],"seq_region_name":"7","id":"rs1794709925","clinical_significance":[]},{"seq_region_name":"7","id":"rs1176214793","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464308,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140464308},{"seq_region_name":"7","id":"rs1585477617","clinical_significance":[],"end":140464309,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140464309,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1232601764","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464310,"source":"dbSNP","strand":1,"feature_type":"variation","end":140464315,"alleles":["GGGAGG","GG"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464315,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140464315,"seq_region_name":"7","id":"rs1794710272","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140464316,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464316,"source":"dbSNP","id":"rs930542603","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794710451","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464318,"source":"dbSNP","strand":1,"feature_type":"variation","end":140464318,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1048384765","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464319,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140464319},{"id":"rs1563091401","seq_region_name":"7","clinical_significance":[],"end":140464323,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140464323,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140464326,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464326,"clinical_significance":[],"seq_region_name":"7","id":"rs1794710694"},{"strand":1,"feature_type":"variation","end":140464328,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464328,"source":"dbSNP","seq_region_name":"7","id":"rs1270776010","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464331,"feature_type":"variation","strand":1,"end":140464331,"alleles":["G","A"],"clinical_significance":[],"id":"rs1794710849","seq_region_name":"7"},{"end":140464336,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140464336,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130294933"},{"clinical_significance":[],"id":"rs1794710917","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464339,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140464339},{"source":"dbSNP","start":140464342,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140464342,"alleles":["T","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794710986"},{"clinical_significance":[],"id":"rs1472930841","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140464345,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464345},{"seq_region_name":"7","id":"rs1220029058","clinical_significance":[],"start":140464347,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140464347,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1639382822","clinical_significance":[],"start":140464348,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140464348,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs185128140","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464354,"source":"dbSNP","strand":1,"feature_type":"variation","end":140464354,"alleles":["C","A","G","T"]},{"id":"rs1411037224","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464355,"source":"dbSNP","strand":1,"feature_type":"variation","end":140464355,"alleles":["G","A","C"]},{"end":140464359,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140464359,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1315143971","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794711488","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464363,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140464363},{"end":140464365,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140464365,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs556009170","seq_region_name":"7"},{"seq_region_name":"7","id":"rs992718426","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140464368,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464368,"source":"dbSNP"},{"source":"dbSNP","start":140464369,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140464369,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585477695"},{"alleles":["AG","AGAG"],"end":140464375,"strand":1,"feature_type":"variation","start":140464374,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1170747918","seq_region_name":"7","clinical_significance":[]},{"end":140464377,"alleles":["C","A","G","T"],"strand":1,"feature_type":"variation","start":140464377,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1019683411","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140464381,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464381,"source":"dbSNP","seq_region_name":"7","id":"rs901238704","clinical_significance":[]},{"id":"rs1794711900","seq_region_name":"7","clinical_significance":[],"start":140464385,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140464385,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464387,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140464387,"clinical_significance":[],"seq_region_name":"7","id":"rs1402444990"},{"seq_region_name":"7","id":"rs1404669773","clinical_significance":[],"start":140464388,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140464388,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1794712090","clinical_significance":[],"end":140464391,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140464391,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130295290","alleles":["C","T"],"end":140464395,"feature_type":"variation","strand":1,"source":"dbSNP","start":140464395,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["T","C"],"end":140464396,"strand":1,"feature_type":"variation","start":140464396,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1361609813","seq_region_name":"7","clinical_significance":[]},{"id":"rs1794712201","seq_region_name":"7","clinical_significance":[],"start":140464398,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140464398,"alleles":["T","-"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1463995152","end":140464414,"alleles":["AAAAAA","AAA","AAAAAAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140464409,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1330427032","clinical_significance":[],"strand":1,"feature_type":"variation","end":140464413,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464413,"source":"dbSNP"},{"seq_region_name":"7","id":"rs2130295367","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464420,"source":"dbSNP","strand":1,"feature_type":"variation","end":140464420,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1359465004","clinical_significance":[],"end":140464423,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140464423,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464425,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140464425,"clinical_significance":[],"seq_region_name":"7","id":"rs997461111"},{"seq_region_name":"7","id":"rs1304763432","clinical_significance":[],"start":140464428,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140464428,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1028459454","alleles":["C","G","T"],"end":140464429,"feature_type":"variation","strand":1,"source":"dbSNP","start":140464429,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140464430,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140464430,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1157823879"},{"feature_type":"variation","strand":1,"end":140464431,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464431,"clinical_significance":[],"seq_region_name":"7","id":"rs969931831"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464432,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140464432,"clinical_significance":[],"seq_region_name":"7","id":"rs980104681"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464434,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140464434,"id":"rs1794712857","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1196873211","seq_region_name":"7","end":140464436,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140464436,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464437,"source":"dbSNP","strand":1,"feature_type":"variation","end":140464437,"alleles":["C","T"],"id":"rs1239753075","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140464441,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464441,"clinical_significance":[],"seq_region_name":"7","id":"rs1490105191"},{"end":140464487,"alleles":["CACCTGTAATCCCAGCACTTTGGGAGGCCGAGGTGGGCGATCACCTG","CACCTG"],"strand":1,"feature_type":"variation","start":140464441,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794713063","clinical_significance":[]},{"alleles":["A","G"],"end":140464442,"strand":1,"feature_type":"variation","start":140464442,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs920558911","clinical_significance":[]},{"clinical_significance":[],"id":"rs958537152","seq_region_name":"7","end":140464443,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140464443,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1484890758","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","A","G"],"end":140464445,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464445},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563091445","source":"dbSNP","start":140464446,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140464446,"alleles":["G","A"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140464449,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140464449,"alleles":["A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1047782639"},{"end":140464451,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140464451,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs989709370"},{"source":"dbSNP","start":140464453,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140464453,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1325786916"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794713582","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464457,"feature_type":"variation","strand":1,"end":140464457,"alleles":["A","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1020648337","alleles":["C","T"],"end":140464458,"feature_type":"variation","strand":1,"source":"dbSNP","start":140464458,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794713699","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464462,"feature_type":"variation","strand":1,"alleles":["GGG","GG"],"end":140464464},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464468,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140464468,"id":"rs966394845","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs981755877","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464469,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140464469},{"alleles":["G","A"],"end":140464470,"feature_type":"variation","strand":1,"source":"dbSNP","start":140464470,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1272773112"},{"source":"dbSNP","start":140464470,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140464491,"alleles":["GAGGTGGGCGATCACCTGAGGT","GAGGT"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1217278984"},{"seq_region_name":"7","id":"rs927738494","clinical_significance":[],"strand":1,"feature_type":"variation","end":140464472,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464472,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1794714254","clinical_significance":[],"start":140464473,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140464473,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1794714335","seq_region_name":"7","feature_type":"variation","strand":1,"end":140464476,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464476},{"seq_region_name":"7","id":"rs1794714432","clinical_significance":[],"alleles":["GGCG","G"],"end":140464479,"strand":1,"feature_type":"variation","start":140464476,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["C","A","T"],"end":140464478,"feature_type":"variation","strand":1,"source":"dbSNP","start":140464478,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs937769443"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464479,"source":"dbSNP","strand":1,"feature_type":"variation","end":140464479,"alleles":["G","A"],"seq_region_name":"7","id":"rs991066934","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140464482,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464482,"source":"dbSNP","seq_region_name":"7","id":"rs1794714737","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140464484,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464484,"source":"dbSNP","seq_region_name":"7","id":"rs920400942","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794714929","alleles":["T","C"],"end":140464486,"feature_type":"variation","strand":1,"source":"dbSNP","start":140464486,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["G","A","T"],"end":140464489,"feature_type":"variation","strand":1,"source":"dbSNP","start":140464489,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs930573307"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1479939209","source":"dbSNP","start":140464492,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140464492,"alleles":["C","A","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1794715248","clinical_significance":[],"end":140464493,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140464493,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["-","CC"],"end":140464493,"strand":1,"feature_type":"variation","start":140464494,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794715318","clinical_significance":[]},{"start":140464494,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140464494,"alleles":["G","C","T"],"strand":1,"feature_type":"variation","id":"rs1794715407","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794715505","clinical_significance":[],"start":140464497,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140464497,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464498,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140464498,"seq_region_name":"7","id":"rs1794715587","clinical_significance":[]},{"alleles":["C","G","T"],"end":140464500,"feature_type":"variation","strand":1,"source":"dbSNP","start":140464500,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1235429981"},{"id":"rs1794715781","seq_region_name":"7","clinical_significance":[],"start":140464501,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140464501,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1047608565","feature_type":"variation","strand":1,"end":140464502,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464502},{"end":140464504,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140464504,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs907781988"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794716035","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140464505,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464505},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464508,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140464508,"clinical_significance":[],"seq_region_name":"7","id":"rs1794716117"},{"seq_region_name":"7","id":"rs1794716173","clinical_significance":[],"alleles":["G","A"],"end":140464512,"strand":1,"feature_type":"variation","start":140464512,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140464515,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140464515,"strand":1,"feature_type":"variation","id":"rs1794716234","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs796314474","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464516,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140464516},{"start":140464519,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140464519,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794716340","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140464520,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464520,"clinical_significance":[],"seq_region_name":"7","id":"rs1485133000"},{"seq_region_name":"7","id":"rs2130296102","clinical_significance":[],"end":140464521,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140464521,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140464527,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464527,"source":"dbSNP","seq_region_name":"7","id":"rs750533992","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464528,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140464528,"id":"rs1794716864","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140464530,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464530,"clinical_significance":[],"id":"rs1260901161","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs940046479","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464531,"feature_type":"variation","strand":1,"end":140464531,"alleles":["C","T"]},{"id":"rs1041019609","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464532,"source":"dbSNP","strand":1,"feature_type":"variation","end":140464532,"alleles":["G","A"]},{"source":"dbSNP","start":140464533,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140464533,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794717085"},{"source":"dbSNP","start":140464534,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140464534,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794717145"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1261355762","end":140464536,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140464536,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1794717279","seq_region_name":"7","feature_type":"variation","strand":1,"end":140464543,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464543},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464546,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140464546,"seq_region_name":"7","id":"rs574292130","clinical_significance":[]},{"seq_region_name":"7","id":"rs901286578","clinical_significance":[],"end":140464547,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140464547,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1253417231","source":"dbSNP","start":140464549,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140464549,"alleles":["A","C"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140464550,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464550,"source":"dbSNP","id":"rs754828567","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794717572","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464553,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140464553},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794717625","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464557,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140464557},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464559,"feature_type":"variation","strand":1,"end":140464559,"alleles":["G","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1326238683"},{"clinical_significance":[],"id":"rs1476806320","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464560,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140464560},{"id":"rs1313978113","seq_region_name":"7","clinical_significance":[],"alleles":["G","A","C"],"end":140464563,"strand":1,"feature_type":"variation","start":140464563,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1000372779","clinical_significance":[],"strand":1,"feature_type":"variation","end":140464564,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464564,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794717853","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464566,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140464566},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563091523","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140464568,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464568},{"seq_region_name":"7","id":"rs1794717965","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464569,"source":"dbSNP","strand":1,"feature_type":"variation","end":140464569,"alleles":["G","T"]},{"seq_region_name":"7","id":"rs1384342717","clinical_significance":[],"alleles":["T","C"],"end":140464570,"strand":1,"feature_type":"variation","start":140464570,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1794718071","clinical_significance":[],"start":140464572,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140464572,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464573,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140464573,"id":"rs781157100","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1468938260","clinical_significance":[],"strand":1,"feature_type":"variation","end":140464574,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464574,"source":"dbSNP"},{"start":140464575,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140464575,"strand":1,"feature_type":"variation","id":"rs1400635600","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs893947708","clinical_significance":[],"end":140464578,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140464578,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140464580,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140464580,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1794718382","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1011068211","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464581,"feature_type":"variation","strand":1,"end":140464581,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1372296024","end":140464584,"alleles":["A","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140464584,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130296568","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464588,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140464588},{"seq_region_name":"7","id":"rs2130296579","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464589,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140464589},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464595,"source":"dbSNP","strand":1,"feature_type":"variation","end":140464595,"alleles":["C","T"],"seq_region_name":"7","id":"rs1794718509","clinical_significance":[]},{"seq_region_name":"7","id":"rs1021240782","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464597,"source":"dbSNP","strand":1,"feature_type":"variation","end":140464597,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs752630346","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140464598,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464598},{"clinical_significance":[],"id":"rs1794718718","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464598,"feature_type":"variation","strand":1,"alleles":["GGGAG","G"],"end":140464602},{"alleles":["G","T"],"end":140464599,"strand":1,"feature_type":"variation","start":140464599,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs371624854","clinical_significance":[]},{"seq_region_name":"7","id":"rs1183113023","clinical_significance":[],"start":140464600,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140464600,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1331940081","clinical_significance":[],"alleles":["G","A"],"end":140464608,"strand":1,"feature_type":"variation","start":140464608,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140464613,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140464613,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794718973","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464615,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140464615,"seq_region_name":"7","id":"rs1458368049","clinical_significance":[]},{"seq_region_name":"7","id":"rs755963094","clinical_significance":[],"alleles":["T","A"],"end":140464618,"strand":1,"feature_type":"variation","start":140464618,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs112920383","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464619,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140464619},{"alleles":["G","A"],"end":140464620,"strand":1,"feature_type":"variation","start":140464620,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1034656358","clinical_significance":[]},{"id":"rs1563091572","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140464624,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464624,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563091577","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464624,"feature_type":"variation","strand":1,"end":140464631,"alleles":["GAACCTGG","G"]},{"seq_region_name":"7","id":"rs1339074983","clinical_significance":[],"end":140464627,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140464627,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1794719462","clinical_significance":[],"strand":1,"feature_type":"variation","end":140464628,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464628,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140464630,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464630,"clinical_significance":[],"id":"rs1298901287","seq_region_name":"7"},{"alleles":["C","T"],"end":140464636,"strand":1,"feature_type":"variation","start":140464636,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1342398221","clinical_significance":[]},{"id":"rs1398730469","seq_region_name":"7","clinical_significance":[],"start":140464637,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140464637,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464638,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140464638,"clinical_significance":[],"id":"rs1794719698","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140464639,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464639,"source":"dbSNP","seq_region_name":"7","id":"rs1794719754","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130296865","end":140464640,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140464640,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464648,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140464648,"seq_region_name":"7","id":"rs1270169582","clinical_significance":[]},{"start":140464649,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140464649,"alleles":["G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794719864","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130296910","clinical_significance":[],"strand":1,"feature_type":"variation","end":140464653,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464653,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1794719925","clinical_significance":[],"end":140464654,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140464654,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140464659,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464659,"clinical_significance":[],"id":"rs777780424","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1352985944","clinical_significance":[],"strand":1,"feature_type":"variation","end":140464660,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464660,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs559641534","alleles":["T","G"],"end":140464661,"feature_type":"variation","strand":1,"source":"dbSNP","start":140464661,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1794720267","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464663,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140464663},{"id":"rs1221350885","seq_region_name":"7","clinical_significance":[],"end":140464666,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140464666,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140464670,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140464670,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130297000","clinical_significance":[]},{"seq_region_name":"7","id":"rs1276941218","clinical_significance":[],"start":140464671,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140464671,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1794720406","clinical_significance":[],"start":140464674,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140464674,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"end":140464675,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140464675,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794720449"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464680,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140464680,"id":"rs1585478225","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","T"],"end":140464683,"feature_type":"variation","strand":1,"source":"dbSNP","start":140464683,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794720558"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464693,"feature_type":"variation","strand":1,"end":140464693,"alleles":["G","A"],"clinical_significance":[],"id":"rs1794720598","seq_region_name":"7"},{"seq_region_name":"7","id":"rs541220348","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464694,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AAA","AAAA"],"end":140464696},{"seq_region_name":"7","id":"rs1794720817","clinical_significance":[],"alleles":["C","A"],"end":140464697,"strand":1,"feature_type":"variation","start":140464697,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140464698,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140464698,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1216807286","clinical_significance":[]},{"clinical_significance":[],"id":"rs1163696492","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140464699,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464699},{"feature_type":"variation","strand":1,"alleles":["A","AA"],"end":140464700,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464700,"clinical_significance":[],"id":"rs1395490218","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140464703,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464703,"source":"dbSNP","seq_region_name":"7","id":"rs959385328","clinical_significance":[]},{"id":"rs1383363741","seq_region_name":"7","clinical_significance":[],"start":140464704,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140464704,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"end":140464712,"alleles":["AAAAAAA","AAAAAAAA"],"strand":1,"feature_type":"variation","start":140464706,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1162879197","clinical_significance":[]},{"id":"rs990560519","seq_region_name":"7","clinical_significance":[],"start":140464709,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140464709,"strand":1,"feature_type":"variation"},{"id":"rs373353800","seq_region_name":"7","clinical_significance":[],"alleles":["AAACAAACAAACAAA","AAACAAACAAA"],"end":140464724,"strand":1,"feature_type":"variation","start":140464710,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140464711,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140464711,"alleles":["A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs533572847","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1264729966","feature_type":"variation","strand":1,"alleles":["AACAA","AA"],"end":140464715,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464711},{"clinical_significance":[],"seq_region_name":"7","id":"rs920437164","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464712,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140464712},{"seq_region_name":"7","id":"rs1794721887","clinical_significance":[],"alleles":["C","G"],"end":140464713,"strand":1,"feature_type":"variation","start":140464713,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140464717,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140464717,"alleles":["C","A","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs951907188"},{"seq_region_name":"7","id":"rs115927984","clinical_significance":[],"end":140464718,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140464718,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464718,"source":"dbSNP","strand":1,"feature_type":"variation","end":140464731,"alleles":["AAACAAAACAAAAC","AAACAAAACAAAACAAAAC"],"seq_region_name":"7","id":"rs1028086842","clinical_significance":[]},{"source":"dbSNP","start":140464719,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AACAA","AA"],"end":140464723,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1794722238","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1247280990","clinical_significance":[],"start":140464721,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140464721,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140464723,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140464723,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1794722385","seq_region_name":"7"},{"start":140464726,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140464726,"strand":1,"feature_type":"variation","id":"rs1794722442","seq_region_name":"7","clinical_significance":[]},{"alleles":["AAAA","AAA"],"end":140464730,"strand":1,"feature_type":"variation","start":140464727,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1350696481","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464730,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140464730,"id":"rs1280842016","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140464731,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464731,"source":"dbSNP","seq_region_name":"7","id":"rs2130297398","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140464735,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464735,"clinical_significance":[],"seq_region_name":"7","id":"rs1236427027"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794722597","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464746,"feature_type":"variation","strand":1,"end":140464746,"alleles":["G","A","T"]},{"start":140464749,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140464749,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs118101705","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1303515142","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464750,"feature_type":"variation","strand":1,"end":140464750,"alleles":["A","G"]},{"end":140464752,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140464752,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1170603247"},{"id":"rs1394192369","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140464755,"alleles":["CC","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464754,"source":"dbSNP"},{"id":"rs1302403902","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464755,"source":"dbSNP","strand":1,"feature_type":"variation","end":140464755,"alleles":["C","A"]},{"alleles":["CA","-"],"end":140464756,"feature_type":"variation","strand":1,"source":"dbSNP","start":140464755,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1491462823"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585478352","end":140464756,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140464756,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs199775052","clinical_significance":[],"start":140464756,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140464768,"alleles":["AAAAAAAAAAAAA","AAAAAAAAAA","AAAAAAAAAAA","AAAAAAAAAAAA","AAAAAAAAAAAAAA","AAAAAAAAAAAAAAA"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1794723319","seq_region_name":"7","alleles":["A","C"],"end":140464757,"feature_type":"variation","strand":1,"source":"dbSNP","start":140464757,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs983843677","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464760,"feature_type":"variation","strand":1,"end":140464760,"alleles":["A","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794723437","feature_type":"variation","strand":1,"alleles":["A","T"],"end":140464764,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464764},{"source":"dbSNP","start":140464767,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140464767,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794723491"},{"source":"dbSNP","start":140464767,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AAT","-"],"end":140464769,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs907975293","seq_region_name":"7"},{"end":140464768,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140464768,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1479623682"},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140464769,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464769,"source":"dbSNP","seq_region_name":"7","id":"rs1268645454","clinical_significance":[]},{"start":140464770,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140464770,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1217973444","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794723816","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464771,"source":"dbSNP","strand":1,"feature_type":"variation","end":140464771,"alleles":["A","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs944784696","source":"dbSNP","start":140464772,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140464772,"alleles":["G","C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794723940","alleles":["T","C"],"end":140464773,"feature_type":"variation","strand":1,"source":"dbSNP","start":140464773,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140464774,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464774,"source":"dbSNP","seq_region_name":"7","id":"rs1794723991","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464776,"source":"dbSNP","strand":1,"feature_type":"variation","end":140464776,"alleles":["T","A"],"seq_region_name":"7","id":"rs1794724044","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs531319074","end":140464782,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140464782,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140464784,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464784,"clinical_significance":[],"seq_region_name":"7","id":"rs2130297798"},{"source":"dbSNP","start":140464786,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140464786,"alleles":["C","A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794724178"},{"seq_region_name":"7","id":"rs1349362811","clinical_significance":[],"start":140464788,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140464788,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs922061496","clinical_significance":[],"alleles":["A","G"],"end":140464790,"strand":1,"feature_type":"variation","start":140464790,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1794724361","seq_region_name":"7","clinical_significance":[],"start":140464791,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140464791,"strand":1,"feature_type":"variation"},{"end":140464792,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140464792,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585478441"},{"start":140464798,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140464798,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1224977123","clinical_significance":[]},{"seq_region_name":"7","id":"rs1399077675","clinical_significance":[],"start":140464799,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140464799,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140464800,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464800,"source":"dbSNP","seq_region_name":"7","id":"rs1794724562","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1317709114","alleles":["C","T"],"end":140464804,"feature_type":"variation","strand":1,"source":"dbSNP","start":140464804,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140464807,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140464807,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794724718","clinical_significance":[]},{"start":140464810,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140464810,"strand":1,"feature_type":"variation","id":"rs932224806","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1041027928","source":"dbSNP","start":140464814,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140464814,"feature_type":"variation","strand":1},{"id":"rs1431345645","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140464820,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464820,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1346943172","source":"dbSNP","start":140464821,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140464821,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140464821,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","AA"],"end":140464821,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794725146"},{"alleles":["CTCT","CT"],"end":140464825,"feature_type":"variation","strand":1,"source":"dbSNP","start":140464822,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs551241286"},{"clinical_significance":[],"id":"rs1794725321","seq_region_name":"7","feature_type":"variation","strand":1,"end":140464826,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464826},{"seq_region_name":"7","id":"rs904201975","clinical_significance":[],"start":140464831,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140464831,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464836,"source":"dbSNP","strand":1,"feature_type":"variation","end":140464836,"alleles":["C","T"],"id":"rs148578872","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1178784141","seq_region_name":"7","source":"dbSNP","start":140464839,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140464839,"alleles":["G","A","T"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464841,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140464841,"seq_region_name":"7","id":"rs1563091723","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1370650017","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464844,"feature_type":"variation","strand":1,"end":140464844,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1794725788","clinical_significance":[],"start":140464845,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140464845,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1240461129","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140464847,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464847,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140464851,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464851,"source":"dbSNP","id":"rs13227264","seq_region_name":"7","clinical_significance":[]},{"id":"rs1287764084","seq_region_name":"7","clinical_significance":[],"alleles":["C","G"],"end":140464858,"strand":1,"feature_type":"variation","start":140464858,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1794726028","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140464860,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464860,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140464861,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464861,"source":"dbSNP","seq_region_name":"7","id":"rs1794726117","clinical_significance":[]},{"source":"dbSNP","start":140464863,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140464863,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs935710442","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140464864,"alleles":["A","C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464864,"clinical_significance":[],"seq_region_name":"7","id":"rs13227268"},{"seq_region_name":"7","id":"rs13221981","clinical_significance":[],"end":140464865,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140464865,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs142011069","feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140464868,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464868},{"clinical_significance":[],"id":"rs1049868741","seq_region_name":"7","alleles":["G","A"],"end":140464869,"feature_type":"variation","strand":1,"source":"dbSNP","start":140464869,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","T"],"end":140464870,"strand":1,"feature_type":"variation","start":140464870,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs529130936","seq_region_name":"7","clinical_significance":[]},{"id":"rs1794726680","seq_region_name":"7","clinical_significance":[],"end":140464882,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140464882,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs188793281","feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140464884,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464884},{"start":140464886,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140464886,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1205165182","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464896,"feature_type":"variation","strand":1,"end":140464896,"alleles":["T","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs893865019"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563091751","source":"dbSNP","start":140464900,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140464900,"feature_type":"variation","strand":1},{"end":140464904,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140464904,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1289894263","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1011118975","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464907,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140464907},{"seq_region_name":"7","id":"rs1321019035","clinical_significance":[],"strand":1,"feature_type":"variation","end":140464908,"alleles":["CA","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464907,"source":"dbSNP"},{"start":140464908,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140464908,"alleles":["A","T"],"strand":1,"feature_type":"variation","id":"rs1453272199","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464909,"feature_type":"variation","strand":1,"end":140464912,"alleles":["GTCT","-"],"clinical_significance":[],"id":"rs1262251919","seq_region_name":"7"},{"source":"dbSNP","start":140464913,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140464913,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1196606000","seq_region_name":"7"},{"start":140464915,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140464915,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585478640","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464916,"feature_type":"variation","strand":1,"end":140464916,"alleles":["C","A","G"],"clinical_significance":[],"id":"rs1042572573","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464920,"source":"dbSNP","strand":1,"feature_type":"variation","end":140464955,"alleles":["AGCTGGGACTACAGGTACACACCACCACACCCAGCT","AGCT"],"seq_region_name":"7","id":"rs2130298400","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464921,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140464921,"id":"rs1794727456","seq_region_name":"7","clinical_significance":[]},{"start":140464924,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140464926,"alleles":["GGG","GG","GGGG"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs375709866","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794727596","clinical_significance":[],"end":140464928,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140464928,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140464932,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140464932,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794727655","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140464933,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464933,"source":"dbSNP","seq_region_name":"7","id":"rs2130298459","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464935,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140464935,"seq_region_name":"7","id":"rs902776416","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1268278105","end":140464937,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140464937,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1585478676","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140464940,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464940},{"seq_region_name":"7","id":"rs1429955434","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140464941,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464941,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1383600485","source":"dbSNP","start":140464946,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140464946,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1338862100","feature_type":"variation","strand":1,"alleles":["C","-"],"end":140464947,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464947},{"start":140464947,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140464947,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794727976","clinical_significance":[]},{"clinical_significance":[],"id":"rs1450684205","seq_region_name":"7","alleles":["C","T"],"end":140464950,"feature_type":"variation","strand":1,"source":"dbSNP","start":140464950,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1405694535","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464956,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140464956},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464958,"feature_type":"variation","strand":1,"end":140464962,"alleles":["TTTTT","TT"],"clinical_significance":[],"id":"rs1171425136","seq_region_name":"7"},{"end":140464960,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140464960,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794728250","clinical_significance":[]},{"clinical_significance":[],"id":"rs1794728303","seq_region_name":"7","source":"dbSNP","start":140464970,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140464970,"alleles":["A","G"],"feature_type":"variation","strand":1},{"end":140464971,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140464971,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794728350","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1411966376","end":140464975,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140464975,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1417824250","alleles":["G","A"],"end":140464976,"feature_type":"variation","strand":1,"source":"dbSNP","start":140464976,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140464977,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140464977,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1003757873","seq_region_name":"7"},{"end":140464979,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140464979,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs778238230","clinical_significance":[]},{"seq_region_name":"7","id":"rs1445833447","clinical_significance":[],"start":140464980,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140464980,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"id":"rs1794728810","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140464982,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464982,"source":"dbSNP"},{"start":140464983,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140464983,"strand":1,"feature_type":"variation","id":"rs1794728866","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1180252852","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464988,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140464988},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794729006","feature_type":"variation","strand":1,"end":140464989,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140464989},{"alleles":["G","A"],"end":140464992,"feature_type":"variation","strand":1,"source":"dbSNP","start":140464992,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1243183911"},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140464993,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140464993,"source":"dbSNP","seq_region_name":"7","id":"rs1035117117","clinical_significance":[]},{"clinical_significance":[],"id":"rs1585478750","seq_region_name":"7","source":"dbSNP","start":140464997,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C","G"],"end":140464997,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130298813","end":140464998,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140464998,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140465001,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140465001,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs150708322"},{"source":"dbSNP","start":140465004,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140465004,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs959041530"},{"seq_region_name":"7","id":"rs192408007","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140465008,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465008,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465011,"source":"dbSNP","strand":1,"feature_type":"variation","end":140465011,"alleles":["G","A"],"id":"rs1794729450","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","T"],"end":140465012,"strand":1,"feature_type":"variation","start":140465012,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1459608064","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465015,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140465015,"id":"rs1794729802","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","A"],"end":140465017,"strand":1,"feature_type":"variation","start":140465017,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1213388232","clinical_significance":[]},{"clinical_significance":[],"id":"rs1794730014","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465018,"feature_type":"variation","strand":1,"end":140465018,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1204783767","clinical_significance":[],"start":140465019,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140465019,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"end":140465021,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140465021,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs80206918"},{"source":"dbSNP","start":140465022,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140465022,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1270693457","seq_region_name":"7"},{"source":"dbSNP","start":140465028,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140465028,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs951793129"},{"seq_region_name":"7","id":"rs1391466215","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465029,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140465029},{"alleles":["C","T"],"end":140465032,"strand":1,"feature_type":"variation","start":140465032,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs569848274","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465034,"source":"dbSNP","strand":1,"feature_type":"variation","end":140465034,"alleles":["G","T"],"seq_region_name":"7","id":"rs1794730469","clinical_significance":[]},{"source":"dbSNP","start":140465036,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140465036,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794730520"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794730570","end":140465037,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140465037,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465047,"source":"dbSNP","strand":1,"feature_type":"variation","end":140465047,"alleles":["G","A"],"seq_region_name":"7","id":"rs1001418521","clinical_significance":[]},{"clinical_significance":[],"id":"rs1407594482","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465051,"feature_type":"variation","strand":1,"end":140465051,"alleles":["A","G"]},{"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140465052,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465052,"clinical_significance":[],"seq_region_name":"7","id":"rs1794730762"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1450480509","end":140465054,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140465054,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1794730869","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465059,"feature_type":"variation","strand":1,"end":140465059,"alleles":["T","G"]},{"alleles":["C","T"],"end":140465064,"strand":1,"feature_type":"variation","start":140465064,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs560471355","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794730978","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140465067,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465067},{"clinical_significance":[],"seq_region_name":"7","id":"rs527549548","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140465068,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465068},{"clinical_significance":[],"seq_region_name":"7","id":"rs1014675408","source":"dbSNP","start":140465071,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140465071,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140465072,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140465072,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794731157"},{"id":"rs771531252","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465077,"source":"dbSNP","strand":1,"feature_type":"variation","end":140465077,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs975998079","clinical_significance":[],"end":140465079,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140465079,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140465080,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140465080,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794731321"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1353112886","feature_type":"variation","strand":1,"alleles":["A","T"],"end":140465088,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465088},{"seq_region_name":"7","id":"rs2130299247","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465089,"source":"dbSNP","strand":1,"feature_type":"variation","end":140465089,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1311915735","source":"dbSNP","start":140465090,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140465090,"alleles":["A","C"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140465091,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465091,"clinical_significance":[],"id":"rs776050451","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140465093,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465093,"source":"dbSNP","seq_region_name":"7","id":"rs555525416","clinical_significance":[]},{"end":140465096,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140465096,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1563091831","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1794731674","clinical_significance":[],"alleles":["T","C"],"end":140465098,"strand":1,"feature_type":"variation","start":140465098,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794731724","source":"dbSNP","start":140465100,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140465100,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs985862732","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465101,"source":"dbSNP","strand":1,"feature_type":"variation","end":140465101,"alleles":["C","G","T"]},{"start":140465102,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140465102,"alleles":["C","A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1284303371","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794731924","source":"dbSNP","start":140465103,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140465103,"alleles":["T","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1357803793","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","C","T"],"end":140465104,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465104},{"seq_region_name":"7","id":"rs573980436","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140465106,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465106,"source":"dbSNP"},{"alleles":["G","A"],"end":140465109,"feature_type":"variation","strand":1,"source":"dbSNP","start":140465109,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs549283233","seq_region_name":"7"},{"alleles":["A","C"],"end":140465113,"feature_type":"variation","strand":1,"source":"dbSNP","start":140465113,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1481449890"},{"clinical_significance":[],"id":"rs1794732258","seq_region_name":"7","alleles":["C","T"],"end":140465114,"feature_type":"variation","strand":1,"source":"dbSNP","start":140465114,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs534963422","clinical_significance":[],"start":140465115,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140465115,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794732426","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465117,"feature_type":"variation","strand":1,"end":140465117,"alleles":["C","T"]},{"clinical_significance":[],"id":"rs1200375699","seq_region_name":"7","source":"dbSNP","start":140465118,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C","G"],"end":140465118,"feature_type":"variation","strand":1},{"alleles":["C","A"],"end":140465120,"feature_type":"variation","strand":1,"source":"dbSNP","start":140465120,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1794732592","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1236061836","feature_type":"variation","strand":1,"end":140465121,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465121},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794732708","alleles":["A","G"],"end":140465122,"feature_type":"variation","strand":1,"source":"dbSNP","start":140465122,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1417570040","source":"dbSNP","start":140465124,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140465124,"alleles":["C","T"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465128,"source":"dbSNP","strand":1,"feature_type":"variation","end":140465128,"alleles":["T","C"],"seq_region_name":"7","id":"rs922114393","clinical_significance":[]},{"id":"rs1369155835","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465129,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140465129},{"seq_region_name":"7","id":"rs1794732923","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465130,"source":"dbSNP","strand":1,"feature_type":"variation","end":140465130,"alleles":["G","A"]},{"start":140465131,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140465131,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs932110373","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140465135,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465135,"clinical_significance":[],"seq_region_name":"7","id":"rs1794733018"},{"clinical_significance":[],"seq_region_name":"7","id":"rs189363804","end":140465140,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140465140,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794733125","alleles":["T","C"],"end":140465142,"feature_type":"variation","strand":1,"source":"dbSNP","start":140465142,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs865906167","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465144,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140465144},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794733248","alleles":["G","T"],"end":140465146,"feature_type":"variation","strand":1,"source":"dbSNP","start":140465146,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["A","G"],"end":140465154,"feature_type":"variation","strand":1,"source":"dbSNP","start":140465154,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs979998645"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794733349","feature_type":"variation","strand":1,"end":140465156,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465156},{"seq_region_name":"7","id":"rs939596502","clinical_significance":[],"start":140465157,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140465157,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"id":"rs925583772","seq_region_name":"7","clinical_significance":[],"start":140465159,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140465159,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130299804","end":140465160,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140465160,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1056745731","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140465165,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465165},{"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140465166,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465166,"source":"dbSNP","seq_region_name":"7","id":"rs1371509767","clinical_significance":[]},{"alleles":["CAGTTGGTCCA","CAGTTGGTCCAGTTGGTCCA"],"end":140465179,"strand":1,"feature_type":"variation","start":140465169,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794733646","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465170,"feature_type":"variation","strand":1,"end":140465170,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1405889435"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465172,"feature_type":"variation","strand":1,"end":140465172,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1162848236"},{"clinical_significance":[],"seq_region_name":"7","id":"rs935581917","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140465174,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465174},{"clinical_significance":[],"seq_region_name":"7","id":"rs895367172","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465175,"feature_type":"variation","strand":1,"end":140465175,"alleles":["G","A","T"]},{"alleles":["A","G"],"end":140465179,"strand":1,"feature_type":"variation","start":140465179,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794733965","clinical_significance":[]},{"seq_region_name":"7","id":"rs755381915","clinical_significance":[],"start":140465183,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140465183,"alleles":["A","C","G"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140465184,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140465184,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1159246182","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794734143","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140465185,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465185},{"id":"rs1405285888","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["CAAAACTCCAAACAA","CAA"],"end":140465199,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465185,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140465186,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465186,"source":"dbSNP","id":"rs1794734268","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794734333","end":140465189,"alleles":["AAAA","AAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140465186,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1181055180","seq_region_name":"7","source":"dbSNP","start":140465187,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140465187,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465190,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140465190,"clinical_significance":[],"id":"rs1794734441","seq_region_name":"7"},{"start":140465190,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140465190,"alleles":["C","-"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794734495","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1480603961","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465194,"feature_type":"variation","strand":1,"end":140465194,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1466542250","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140465197,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465197},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794734649","feature_type":"variation","strand":1,"end":140465199,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465199},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465203,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140465203,"seq_region_name":"7","id":"rs1220145575","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140465208,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465208,"clinical_significance":[],"id":"rs1563091893","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130300153","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465214,"feature_type":"variation","strand":1,"end":140465214,"alleles":["C","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465216,"feature_type":"variation","strand":1,"end":140465216,"alleles":["G","C"],"clinical_significance":[],"id":"rs1488137957","seq_region_name":"7"},{"start":140465218,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140465218,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794734873","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794734935","source":"dbSNP","start":140465220,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140465220,"alleles":["A","G"],"feature_type":"variation","strand":1},{"alleles":["G","C"],"end":140465221,"feature_type":"variation","strand":1,"source":"dbSNP","start":140465221,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs578196028"},{"id":"rs1794735049","seq_region_name":"7","clinical_significance":[],"end":140465222,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140465222,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140465225,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140465225,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs761236190","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1027724859","feature_type":"variation","strand":1,"end":140465226,"alleles":["G","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465226},{"seq_region_name":"7","id":"rs1794735256","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465228,"source":"dbSNP","strand":1,"feature_type":"variation","end":140465228,"alleles":["T","C"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465230,"feature_type":"variation","strand":1,"end":140465230,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794735319"},{"alleles":["T","C"],"end":140465231,"feature_type":"variation","strand":1,"source":"dbSNP","start":140465231,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794735367"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465234,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140465234,"seq_region_name":"7","id":"rs367787651","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1004566410","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465236,"feature_type":"variation","strand":1,"end":140465236,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs1347762559","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465237,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CCTGTAATCC","CCTGTAATCCTGTAATCC"],"end":140465246},{"end":140465248,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140465248,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1014725989","clinical_significance":[]},{"seq_region_name":"7","id":"rs1363335515","clinical_significance":[],"start":140465249,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140465249,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"start":140465249,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140465249,"alleles":["A","AA"],"strand":1,"feature_type":"variation","id":"rs1404845113","seq_region_name":"7","clinical_significance":[]},{"end":140465254,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140465254,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs879657559","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794735754","source":"dbSNP","start":140465254,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140465258,"alleles":["TTTGG","-"],"feature_type":"variation","strand":1},{"alleles":["T","C"],"end":140465255,"feature_type":"variation","strand":1,"source":"dbSNP","start":140465255,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1454858675","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1341871144","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140465258,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465258,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1794735907","clinical_significance":[],"strand":1,"feature_type":"variation","end":140465259,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465259,"source":"dbSNP"},{"end":140465261,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140465261,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1157888150","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465261,"source":"dbSNP","strand":1,"feature_type":"variation","end":140465262,"alleles":["GG","G"],"seq_region_name":"7","id":"rs1794736031","clinical_significance":[]},{"seq_region_name":"7","id":"rs1470052325","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140465263,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465263,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465264,"source":"dbSNP","strand":1,"feature_type":"variation","end":140465264,"alleles":["C","T"],"id":"rs1230988872","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1292128285","clinical_significance":[],"alleles":["G","A","C"],"end":140465265,"strand":1,"feature_type":"variation","start":140465265,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140465267,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140465267,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794736273"},{"clinical_significance":[],"id":"rs1794736330","seq_region_name":"7","source":"dbSNP","start":140465269,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140465269,"alleles":["C","G","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1197069176","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140465272,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465272,"source":"dbSNP"},{"source":"dbSNP","start":140465273,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140465273,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585479168"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465275,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140465275,"clinical_significance":[],"id":"rs965881728","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1794736622","clinical_significance":[],"alleles":["TTACTT","TT"],"end":140465282,"strand":1,"feature_type":"variation","start":140465277,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs139063128","clinical_significance":[],"alleles":["G","A"],"end":140465285,"strand":1,"feature_type":"variation","start":140465285,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465287,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140465287,"seq_region_name":"7","id":"rs905606422","clinical_significance":[]},{"start":140465291,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140465291,"strand":1,"feature_type":"variation","id":"rs778490317","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1049365654","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140465298,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465298},{"source":"dbSNP","start":140465299,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140465299,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794736940"},{"alleles":["C","G","T"],"end":140465306,"strand":1,"feature_type":"variation","start":140465306,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs576253569","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140465307,"alleles":["T","TT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465307,"source":"dbSNP","seq_region_name":"7","id":"rs1255945058","clinical_significance":[]},{"alleles":["G","A"],"end":140465308,"strand":1,"feature_type":"variation","start":140465308,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1325974266","clinical_significance":[]},{"id":"rs191102924","seq_region_name":"7","clinical_significance":[],"start":140465310,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140465310,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs561487486","clinical_significance":[],"start":140465313,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140465313,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465326,"feature_type":"variation","strand":1,"end":140465327,"alleles":["CT","-"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794737215"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794737263","alleles":["T","C"],"end":140465327,"feature_type":"variation","strand":1,"source":"dbSNP","start":140465327,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465328,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140465328,"seq_region_name":"7","id":"rs1794737315","clinical_significance":[]},{"source":"dbSNP","start":140465332,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140465332,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794737362"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465333,"source":"dbSNP","strand":1,"feature_type":"variation","end":140465333,"alleles":["T","C"],"id":"rs1794737471","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465337,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140465337,"seq_region_name":"7","id":"rs1257184164","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140465339,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465339,"source":"dbSNP","seq_region_name":"7","id":"rs1444326729","clinical_significance":[]},{"source":"dbSNP","start":140465341,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140465341,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs866130112"},{"id":"rs1794737711","seq_region_name":"7","clinical_significance":[],"start":140465342,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140465342,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1794737777","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465344,"feature_type":"variation","strand":1,"end":140465344,"alleles":["A","C","G"]},{"seq_region_name":"7","id":"rs528899678","clinical_significance":[],"end":140465345,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140465345,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1794737934","seq_region_name":"7","clinical_significance":[],"start":140465346,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140465346,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1794737985","clinical_significance":[],"start":140465347,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140465347,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1794738042","clinical_significance":[],"strand":1,"feature_type":"variation","end":140465350,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465350,"source":"dbSNP"},{"seq_region_name":"7","id":"rs547346879","clinical_significance":[],"start":140465351,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140465351,"alleles":["T","G"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140465352,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140465352,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1381040212"},{"seq_region_name":"7","id":"rs1794738203","clinical_significance":[],"strand":1,"feature_type":"variation","end":140465360,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465360,"source":"dbSNP"},{"id":"rs1794738273","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465361,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140465361},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465363,"feature_type":"variation","strand":1,"end":140465363,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs559251369"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794738363","source":"dbSNP","start":140465366,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140465366,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1359243086","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140465367,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465367,"source":"dbSNP"},{"start":140465386,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140465386,"alleles":["C","G"],"strand":1,"feature_type":"variation","id":"rs1794738497","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465389,"feature_type":"variation","strand":1,"end":140465389,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1256828332"},{"start":140465392,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140465392,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs149904769","clinical_significance":[]},{"id":"rs1563091967","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","CC"],"end":140465392,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465392,"source":"dbSNP"},{"start":140465393,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140465393,"strand":1,"feature_type":"variation","id":"rs567691578","seq_region_name":"7","clinical_significance":[]},{"start":140465397,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140465397,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs1794738822","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794738874","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140465402,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465402},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465408,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140465408,"seq_region_name":"7","id":"rs1794738923","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140465411,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465411,"clinical_significance":[],"seq_region_name":"7","id":"rs371500114"},{"clinical_significance":[],"seq_region_name":"7","id":"rs966011900","alleles":["G","A"],"end":140465416,"feature_type":"variation","strand":1,"source":"dbSNP","start":140465416,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140465418,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140465418,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs768938697"},{"seq_region_name":"7","id":"rs1794739147","clinical_significance":[],"start":140465421,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","TT"],"end":140465421,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465424,"feature_type":"variation","strand":1,"end":140465424,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs776990486"},{"source":"dbSNP","start":140465426,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140465426,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1173848228","seq_region_name":"7"},{"end":140465427,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140465427,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1373443154","clinical_significance":[]},{"clinical_significance":[],"id":"rs1465298659","seq_region_name":"7","end":140465439,"alleles":["TGCACCACTGCAC","TGCAC"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140465427,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","T"],"end":140465437,"strand":1,"feature_type":"variation","start":140465437,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130301139","clinical_significance":[]},{"end":140465441,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140465441,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1461839812"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1426730296","feature_type":"variation","strand":1,"end":140465442,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465442},{"seq_region_name":"7","id":"rs1794739484","clinical_significance":[],"alleles":["C","A"],"end":140465446,"strand":1,"feature_type":"variation","start":140465446,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140465451,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140465451,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs146463356","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794739608","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465452,"feature_type":"variation","strand":1,"end":140465452,"alleles":["G","A"]},{"end":140465454,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140465454,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs113064536","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465456,"source":"dbSNP","strand":1,"feature_type":"variation","end":140465456,"alleles":["G","A"],"seq_region_name":"7","id":"rs1057030092","clinical_significance":[]},{"start":140465459,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140465459,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794739801","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465462,"source":"dbSNP","strand":1,"feature_type":"variation","end":140465462,"alleles":["G","A"],"seq_region_name":"7","id":"rs895431255","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs948268664","end":140465463,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140465463,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1481132863","source":"dbSNP","start":140465465,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140465465,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1048723147","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465466,"feature_type":"variation","strand":1,"end":140465466,"alleles":["C","G"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465471,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","TT"],"end":140465471,"seq_region_name":"7","id":"rs1253513075","clinical_significance":[]},{"seq_region_name":"7","id":"rs1340544548","clinical_significance":[],"alleles":["T","-"],"end":140465471,"strand":1,"feature_type":"variation","start":140465471,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140465471,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465471,"clinical_significance":[],"id":"rs1794740106","seq_region_name":"7"},{"end":140465480,"alleles":["AAAAAAAAA","AAAAAAAA","AAAAAAAAAA","AAAAAAAAAAAAAAAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140465472,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs979665622","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140465473,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465473,"source":"dbSNP","seq_region_name":"7","id":"rs925437815","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794740415","source":"dbSNP","start":140465474,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G","T"],"end":140465474,"feature_type":"variation","strand":1},{"id":"rs1794740489","seq_region_name":"7","clinical_significance":[],"start":140465478,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140465478,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1794740549","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465478,"source":"dbSNP","strand":1,"feature_type":"variation","end":140465487,"alleles":["AAAGAAAGAA","AAAGAA"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794740612","feature_type":"variation","strand":1,"end":140465479,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465479},{"seq_region_name":"7","id":"rs1024504195","clinical_significance":[],"start":140465481,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140465481,"strand":1,"feature_type":"variation"},{"alleles":["A","G"],"end":140465482,"feature_type":"variation","strand":1,"source":"dbSNP","start":140465482,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794740706"},{"seq_region_name":"7","id":"rs1293393854","clinical_significance":[],"alleles":["AAGAAG","AAG"],"end":140465488,"strand":1,"feature_type":"variation","start":140465483,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs887416545","seq_region_name":"7","feature_type":"variation","strand":1,"end":140465485,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465485},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794740855","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465486,"feature_type":"variation","strand":1,"end":140465486,"alleles":["A","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465487,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140465487,"id":"rs1794740912","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","A"],"end":140465488,"feature_type":"variation","strand":1,"source":"dbSNP","start":140465488,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794740964"},{"source":"dbSNP","start":140465492,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140465492,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585479430"},{"end":140465493,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140465493,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1306821655","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140465494,"alleles":["C","A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465494,"clinical_significance":[],"seq_region_name":"7","id":"rs906024288"},{"seq_region_name":"7","id":"rs1794741198","clinical_significance":[],"alleles":["A","G"],"end":140465501,"strand":1,"feature_type":"variation","start":140465501,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140465504,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465504,"source":"dbSNP","seq_region_name":"7","id":"rs2130301500","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794741260","clinical_significance":[],"strand":1,"feature_type":"variation","end":140465507,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465507,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465508,"source":"dbSNP","strand":1,"feature_type":"variation","end":140465508,"alleles":["C","T"],"seq_region_name":"7","id":"rs1257531525","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794741368","source":"dbSNP","start":140465511,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140465511,"alleles":["T","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1334218612","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465514,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140465514},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465514,"feature_type":"variation","strand":1,"end":140465517,"alleles":["CCCC","CCC"],"clinical_significance":[],"seq_region_name":"7","id":"rs1384368614"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465515,"source":"dbSNP","strand":1,"feature_type":"variation","end":140465515,"alleles":["C","T"],"seq_region_name":"7","id":"rs1395151289","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465519,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140465519,"seq_region_name":"7","id":"rs1396939683","clinical_significance":[]},{"seq_region_name":"7","id":"rs1004494231","clinical_significance":[],"start":140465521,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140465521,"alleles":["G","A","C"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140465521,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["GGG","GG"],"end":140465523,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794741690"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1350344050","end":140465523,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140465523,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1208941785","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465535,"source":"dbSNP","strand":1,"feature_type":"variation","end":140465537,"alleles":["AAA","A"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465538,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140465538,"seq_region_name":"7","id":"rs1460383355","clinical_significance":[]},{"clinical_significance":[],"id":"rs1164168425","seq_region_name":"7","feature_type":"variation","strand":1,"end":140465540,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465540},{"clinical_significance":[],"seq_region_name":"7","id":"rs1366086576","end":140465542,"alleles":["TG","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140465541,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140465543,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140465543,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130301690","clinical_significance":[]},{"seq_region_name":"7","id":"rs988773337","clinical_significance":[],"end":140465544,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140465544,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465549,"source":"dbSNP","strand":1,"feature_type":"variation","end":140465549,"alleles":["C","G","T"],"id":"rs549462653","seq_region_name":"7","clinical_significance":[]},{"end":140465565,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140465565,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794742166","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794742223","feature_type":"variation","strand":1,"end":140465573,"alleles":["ATACTA","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465568},{"seq_region_name":"7","id":"rs1253069659","clinical_significance":[],"alleles":["T","C"],"end":140465569,"strand":1,"feature_type":"variation","start":140465569,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs138435986","end":140465580,"alleles":["ACTAGACTAGA","ACTAGA","ACTAGACTAGACTAGA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140465570,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140465572,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140465572,"alleles":["T","A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1794742437","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585479548","feature_type":"variation","strand":1,"end":140465574,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465574},{"clinical_significance":[],"seq_region_name":"7","id":"rs1482949204","alleles":["T","C"],"end":140465577,"feature_type":"variation","strand":1,"source":"dbSNP","start":140465577,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1293051978","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140465579,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465579},{"start":140465580,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140465580,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1225383020","clinical_significance":[]},{"source":"dbSNP","start":140465581,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140465581,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1045354014"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465584,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140465584,"seq_region_name":"7","id":"rs1281987783","clinical_significance":[]},{"clinical_significance":[],"id":"rs1243572994","seq_region_name":"7","end":140465585,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140465585,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs2130301883","seq_region_name":"7","end":140465590,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140465590,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465592,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140465592,"seq_region_name":"7","id":"rs1014652542","clinical_significance":[]},{"source":"dbSNP","start":140465593,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140465593,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1308726232","seq_region_name":"7"},{"start":140465594,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140465594,"strand":1,"feature_type":"variation","id":"rs1794743016","seq_region_name":"7","clinical_significance":[]},{"id":"rs567515517","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465596,"source":"dbSNP","strand":1,"feature_type":"variation","end":140465596,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1407723630","feature_type":"variation","strand":1,"end":140465597,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465597},{"start":140465599,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140465599,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794743159","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140465603,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465603,"source":"dbSNP","seq_region_name":"7","id":"rs1585479604","clinical_significance":[]},{"start":140465605,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140465605,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","id":"rs901601200","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs997393353","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465606,"source":"dbSNP","strand":1,"feature_type":"variation","end":140465606,"alleles":["G","A","T"]},{"source":"dbSNP","start":140465607,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140465607,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1794743397","seq_region_name":"7"},{"seq_region_name":"7","id":"rs927084689","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140465610,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465610,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1363788456","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465617,"feature_type":"variation","strand":1,"end":140465617,"alleles":["A","C","T"]},{"end":140465620,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140465620,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1794743572","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140465621,"alleles":["G","C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465621,"source":"dbSNP","seq_region_name":"7","id":"rs535037008","clinical_significance":[]},{"end":140465622,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140465622,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794743714"},{"clinical_significance":[],"seq_region_name":"7","id":"rs553678681","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465623,"feature_type":"variation","strand":1,"end":140465623,"alleles":["C","A"]},{"id":"rs1794743830","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465624,"source":"dbSNP","strand":1,"feature_type":"variation","end":140465624,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs758183727","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465626,"source":"dbSNP","strand":1,"feature_type":"variation","end":140465626,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs578260593","source":"dbSNP","start":140465628,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140465628,"alleles":["C","T"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140465637,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465637,"source":"dbSNP","seq_region_name":"7","id":"rs1794744019","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465638,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140465638,"seq_region_name":"7","id":"rs1794744072","clinical_significance":[]},{"end":140465640,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140465640,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1022315771","clinical_significance":[]},{"id":"rs1472434055","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140465641,"alleles":["C","A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465641,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["CC","CCC"],"end":140465645,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465644,"source":"dbSNP","seq_region_name":"7","id":"rs1794744303","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794744354","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140465645,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465645,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140465646,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465646,"clinical_significance":[],"seq_region_name":"7","id":"rs1585479691"},{"seq_region_name":"7","id":"rs116168613","clinical_significance":[],"strand":1,"feature_type":"variation","end":140465648,"alleles":["T","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465648,"source":"dbSNP"},{"alleles":["C","A","G","T"],"end":140465650,"feature_type":"variation","strand":1,"source":"dbSNP","start":140465650,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs978066262"},{"seq_region_name":"7","id":"rs924061784","clinical_significance":[],"alleles":["G","A","T"],"end":140465651,"strand":1,"feature_type":"variation","start":140465651,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1379673532","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140465652,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465652,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1208676796","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465652,"source":"dbSNP","strand":1,"feature_type":"variation","end":140465654,"alleles":["AAA","AA","AAAA"]},{"end":140465657,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140465657,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs961067424"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140465663,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465663,"source":"dbSNP","id":"rs1794744887","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794744944","clinical_significance":[],"end":140465672,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140465672,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1226206784","seq_region_name":"7","source":"dbSNP","start":140465672,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["CTCTC","CTC"],"end":140465676,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794745069","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465677,"feature_type":"variation","strand":1,"end":140465678,"alleles":["AA","AAA"]},{"source":"dbSNP","start":140465678,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140465678,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794745129"},{"seq_region_name":"7","id":"rs1349640764","clinical_significance":[],"start":140465681,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140465681,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1563092106","clinical_significance":[],"alleles":["T","C"],"end":140465682,"strand":1,"feature_type":"variation","start":140465682,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs992345835","clinical_significance":[],"strand":1,"feature_type":"variation","end":140465685,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465685,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1794745347","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140465689,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465689},{"seq_region_name":"7","id":"rs1794745412","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465691,"source":"dbSNP","strand":1,"feature_type":"variation","end":140465691,"alleles":["T","C"]},{"start":140465696,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["CTATC","CTATCTATC"],"end":140465700,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794745485","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140465700,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465700,"source":"dbSNP","seq_region_name":"7","id":"rs1794745535","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140465704,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465704,"clinical_significance":[],"seq_region_name":"7","id":"rs1794745582"},{"id":"rs750654604","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140465705,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465705,"source":"dbSNP"},{"id":"rs1794745717","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465709,"source":"dbSNP","strand":1,"feature_type":"variation","end":140465709,"alleles":["T","C"]},{"source":"dbSNP","start":140465712,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140465712,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs557546267"},{"feature_type":"variation","strand":1,"end":140465714,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465714,"clinical_significance":[],"id":"rs1794745839","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794745904","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465717,"feature_type":"variation","strand":1,"end":140465717,"alleles":["C","A","G","T"]},{"strand":1,"feature_type":"variation","end":140465719,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465719,"source":"dbSNP","id":"rs1794745987","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794746043","clinical_significance":[],"start":140465720,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140465720,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1794746112","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465721,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140465721},{"clinical_significance":[],"id":"rs1283766399","seq_region_name":"7","feature_type":"variation","strand":1,"end":140465722,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465722},{"seq_region_name":"7","id":"rs1406667946","clinical_significance":[],"end":140465724,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140465724,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1172584931","clinical_significance":[],"start":140465728,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140465728,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1794746331","clinical_significance":[],"end":140465735,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140465735,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140465736,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465736,"clinical_significance":[],"seq_region_name":"7","id":"rs1794746378"},{"alleles":["G","A"],"end":140465737,"strand":1,"feature_type":"variation","start":140465737,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794746437","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140465740,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465740,"clinical_significance":[],"seq_region_name":"7","id":"rs916695387"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465741,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140465741,"clinical_significance":[],"id":"rs1794746569","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs575806620","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140465742,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465742},{"seq_region_name":"7","id":"rs1322843026","clinical_significance":[],"end":140465744,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140465744,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465745,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140465745,"id":"rs1794746724","seq_region_name":"7","clinical_significance":[]},{"start":140465746,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140465748,"alleles":["GGG","GG"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1401287539","clinical_significance":[]},{"clinical_significance":[],"id":"rs1794746844","seq_region_name":"7","end":140465753,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140465753,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs948344705","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465755,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140465755},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465765,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140465765,"clinical_significance":[],"id":"rs1794746953","seq_region_name":"7"},{"id":"rs1387246612","seq_region_name":"7","clinical_significance":[],"start":140465766,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140465768,"alleles":["AAA","A"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140465769,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465769,"source":"dbSNP","seq_region_name":"7","id":"rs1794747065","clinical_significance":[]},{"clinical_significance":[],"id":"rs1004821728","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465770,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140465770},{"end":140465774,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140465774,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1585479825","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","C"],"end":140465780,"feature_type":"variation","strand":1,"source":"dbSNP","start":140465780,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794747229"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1036661556","alleles":["C","A","T"],"end":140465781,"feature_type":"variation","strand":1,"source":"dbSNP","start":140465781,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140465782,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140465782,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794747367","clinical_significance":[]},{"start":140465783,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140465782,"alleles":["-","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794747462","clinical_significance":[]},{"seq_region_name":"7","id":"rs1049330161","clinical_significance":[],"start":140465787,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140465787,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140465790,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465790,"source":"dbSNP","seq_region_name":"7","id":"rs909450813","clinical_significance":[]},{"seq_region_name":"7","id":"rs940400395","clinical_significance":[],"strand":1,"feature_type":"variation","end":140465795,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465795,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465797,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140465797,"clinical_significance":[],"id":"rs1202106164","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130302872","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140465798,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465798},{"clinical_significance":[],"seq_region_name":"7","id":"rs1476726399","feature_type":"variation","strand":1,"end":140465799,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465799},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465800,"source":"dbSNP","strand":1,"feature_type":"variation","end":140465800,"alleles":["G","A"],"id":"rs2130302891","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140465803,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465803,"source":"dbSNP","seq_region_name":"7","id":"rs1035981156","clinical_significance":[]},{"source":"dbSNP","start":140465804,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140465804,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs543116880","seq_region_name":"7"},{"seq_region_name":"7","id":"rs763070213","clinical_significance":[],"start":140465805,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140465805,"alleles":["G","C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1794748021","clinical_significance":[],"alleles":["G","A"],"end":140465806,"strand":1,"feature_type":"variation","start":140465806,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1447022593","clinical_significance":[],"strand":1,"feature_type":"variation","end":140465808,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465808,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465809,"source":"dbSNP","strand":1,"feature_type":"variation","end":140465809,"alleles":["T","C"],"seq_region_name":"7","id":"rs1263298948","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140465811,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465811,"clinical_significance":[],"id":"rs997637519","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465812,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140465812,"seq_region_name":"7","id":"rs1794748272","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794748338","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140465813,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465813,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1286594617","source":"dbSNP","start":140465815,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140465815,"alleles":["C","T"],"feature_type":"variation","strand":1},{"alleles":["C","G"],"end":140465817,"strand":1,"feature_type":"variation","start":140465817,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130303024","clinical_significance":[]},{"id":"rs2130303039","seq_region_name":"7","clinical_significance":[],"end":140465818,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140465818,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1361265284","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465819,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140465819},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465820,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140465820,"id":"rs777547513","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","A"],"end":140465821,"strand":1,"feature_type":"variation","start":140465821,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794748627","clinical_significance":[]},{"start":140465822,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140465822,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs953478456","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","A"],"end":140465829,"feature_type":"variation","strand":1,"source":"dbSNP","start":140465829,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1342654445"},{"clinical_significance":[],"seq_region_name":"7","id":"rs111654741","end":140465833,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140465833,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140465834,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","G","T"],"end":140465834,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1274130345"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465835,"source":"dbSNP","strand":1,"feature_type":"variation","end":140465835,"alleles":["C","A","T"],"seq_region_name":"7","id":"rs888916292","clinical_significance":[]},{"end":140465836,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140465836,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794749022"},{"seq_region_name":"7","id":"rs1794749079","clinical_significance":[],"strand":1,"feature_type":"variation","end":140465838,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465838,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794749133","feature_type":"variation","strand":1,"end":140465840,"alleles":["G","C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465840},{"seq_region_name":"7","id":"rs1794749208","clinical_significance":[],"end":140465851,"alleles":["GAGGCCGAGG","GAGG"],"strand":1,"feature_type":"variation","start":140465842,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140465843,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140465843,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585479943","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794749311","source":"dbSNP","start":140465845,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140465845,"alleles":["G","A"],"feature_type":"variation","strand":1},{"id":"rs1368470284","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140465846,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465846,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs374119836","source":"dbSNP","start":140465846,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["CC","C"],"end":140465847,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs550288356","feature_type":"variation","strand":1,"end":140465847,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465847},{"end":140465848,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140465848,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1279942852"},{"seq_region_name":"7","id":"rs1794749643","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465849,"source":"dbSNP","strand":1,"feature_type":"variation","end":140465849,"alleles":["A","C"]},{"seq_region_name":"7","id":"rs573535781","clinical_significance":[],"strand":1,"feature_type":"variation","end":140465851,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465851,"source":"dbSNP"},{"clinical_significance":[],"id":"rs2130303318","seq_region_name":"7","feature_type":"variation","strand":1,"end":140465852,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465852},{"end":140465855,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140465855,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1178858760","clinical_significance":[]},{"alleles":["C","A","T"],"end":140465856,"feature_type":"variation","strand":1,"source":"dbSNP","start":140465856,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs572457657"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465857,"source":"dbSNP","strand":1,"feature_type":"variation","end":140465857,"alleles":["G","A","C"],"id":"rs1424931192","seq_region_name":"7","clinical_significance":[]},{"end":140465858,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140465858,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs752680880","clinical_significance":[]},{"source":"dbSNP","start":140465858,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140465859,"alleles":["GA","GAGA"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794750041"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1168973941","end":140465872,"alleles":["GATCAGGAGGTCAGA","GA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140465858,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1374285992","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465859,"source":"dbSNP","strand":1,"feature_type":"variation","end":140465859,"alleles":["A","G"]},{"start":140465863,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140465863,"alleles":["G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130303415","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465864,"source":"dbSNP","strand":1,"feature_type":"variation","end":140465864,"alleles":["G","A"],"id":"rs571609081","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794750268","feature_type":"variation","strand":1,"end":140465865,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465865},{"start":140465868,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140465868,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585480002","clinical_significance":[]},{"end":140465872,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140465872,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1563092210","clinical_significance":[]},{"clinical_significance":[],"id":"rs559211787","seq_region_name":"7","end":140465873,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140465873,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465874,"source":"dbSNP","strand":1,"feature_type":"variation","end":140465874,"alleles":["G","A"],"seq_region_name":"7","id":"rs1218123786","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794750570","source":"dbSNP","start":140465875,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140465875,"alleles":["A","G"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140465877,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465877,"source":"dbSNP","seq_region_name":"7","id":"rs756125970","clinical_significance":[]},{"seq_region_name":"7","id":"rs988312817","clinical_significance":[],"strand":1,"feature_type":"variation","end":140465878,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465878,"source":"dbSNP"},{"end":140465881,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140465881,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1277707136"},{"alleles":["C","T"],"end":140465883,"strand":1,"feature_type":"variation","start":140465883,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1030972183","clinical_significance":[]},{"clinical_significance":[],"id":"rs1794750933","seq_region_name":"7","source":"dbSNP","start":140465887,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140465887,"alleles":["C","A"],"feature_type":"variation","strand":1},{"end":140465888,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140465888,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs918191497"},{"start":140465891,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140465891,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794751045","clinical_significance":[]},{"id":"rs970951118","seq_region_name":"7","clinical_significance":[],"start":140465892,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140465892,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465895,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140465895,"clinical_significance":[],"seq_region_name":"7","id":"rs1794751105"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465896,"source":"dbSNP","strand":1,"feature_type":"variation","end":140465896,"alleles":["A","G"],"id":"rs1210905479","seq_region_name":"7","clinical_significance":[]},{"id":"rs981106799","seq_region_name":"7","clinical_significance":[],"start":140465897,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A","C"],"end":140465897,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140465899,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465899,"clinical_significance":[],"seq_region_name":"7","id":"rs184674199"},{"seq_region_name":"7","id":"rs1794751284","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465902,"source":"dbSNP","strand":1,"feature_type":"variation","end":140465904,"alleles":["AAA","AA"]},{"clinical_significance":[],"id":"rs1383659342","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465906,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140465906},{"seq_region_name":"7","id":"rs1338888085","clinical_significance":[],"start":140465907,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140465907,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs6964170","feature_type":"variation","strand":1,"end":140465908,"alleles":["T","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465908},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794751576","end":140465909,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140465909,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465912,"source":"dbSNP","strand":1,"feature_type":"variation","end":140465912,"alleles":["T","G"],"seq_region_name":"7","id":"rs1794751639","clinical_significance":[]},{"alleles":["T","C"],"end":140465913,"strand":1,"feature_type":"variation","start":140465913,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1563092245","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794751758","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465916,"feature_type":"variation","strand":1,"end":140465916,"alleles":["C","T"]},{"start":140465917,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140465917,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794751814","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140465924,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465924,"clinical_significance":[],"seq_region_name":"7","id":"rs1794751868"},{"clinical_significance":[],"id":"rs1193373598","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["AAAAAAA","AAAAAA","AAAAAAAA"],"end":140465931,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465925},{"strand":1,"feature_type":"variation","end":140465927,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465927,"source":"dbSNP","seq_region_name":"7","id":"rs1794752009","clinical_significance":[]},{"start":140465929,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140465929,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1330048523","clinical_significance":[]},{"end":140465931,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140465931,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585480106"},{"start":140465933,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140465933,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs770794143","clinical_significance":[]},{"end":140465934,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140465934,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs563101620"},{"seq_region_name":"7","id":"rs937110461","clinical_significance":[],"strand":1,"feature_type":"variation","end":140465938,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465938,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794752362","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465941,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140465941},{"seq_region_name":"7","id":"rs1441150480","clinical_significance":[],"start":140465942,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C","G"],"end":140465942,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465945,"feature_type":"variation","strand":1,"end":140465945,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs916657519"},{"clinical_significance":[],"seq_region_name":"7","id":"rs189539366","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140465947,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465947},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465951,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140465951,"clinical_significance":[],"id":"rs1448302555","seq_region_name":"7"},{"clinical_significance":[],"id":"rs984921965","seq_region_name":"7","feature_type":"variation","strand":1,"end":140465952,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465952},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794752744","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465952,"feature_type":"variation","strand":1,"alleles":["G","GG"],"end":140465952},{"clinical_significance":[],"id":"rs1385374792","seq_region_name":"7","feature_type":"variation","strand":1,"end":140465954,"alleles":["GCG","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465952},{"strand":1,"feature_type":"variation","end":140465953,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465953,"source":"dbSNP","id":"rs909503049","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140465953,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140465953,"alleles":["C","CCTCAGCC"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1471645887"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794752951","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465954,"feature_type":"variation","strand":1,"end":140465953,"alleles":["-","CTCA"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs940915090","source":"dbSNP","start":140465954,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140465954,"alleles":["G","A","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794753068","feature_type":"variation","strand":1,"end":140465955,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465955},{"seq_region_name":"7","id":"rs1794753127","clinical_significance":[],"start":140465955,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140465957,"alleles":["CCT","CCTCCT"],"strand":1,"feature_type":"variation"},{"alleles":["T","A"],"end":140465957,"strand":1,"feature_type":"variation","start":140465957,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1439348804","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140465959,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140465959,"alleles":["T","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1272337919","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1204376356","seq_region_name":"7","alleles":["T","G"],"end":140465962,"feature_type":"variation","strand":1,"source":"dbSNP","start":140465962,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794753358","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465962,"feature_type":"variation","strand":1,"alleles":["TCCCA","-"],"end":140465966},{"source":"dbSNP","start":140465964,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140465964,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1458377633"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465964,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CCAGCT","-"],"end":140465969,"id":"rs1794753488","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794753549","end":140465969,"alleles":["T","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140465969,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140465971,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465971,"source":"dbSNP","seq_region_name":"7","id":"rs1794753609","clinical_significance":[]},{"source":"dbSNP","start":140465973,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140465973,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1317300442"},{"source":"dbSNP","start":140465976,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140465976,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794753720"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465976,"feature_type":"variation","strand":1,"alleles":["GAG","GAGAG"],"end":140465978,"clinical_significance":[],"seq_region_name":"7","id":"rs2130304191"},{"id":"rs1794753777","seq_region_name":"7","clinical_significance":[],"start":140465977,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140465977,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1794753834","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140465980,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140465980},{"clinical_significance":[],"seq_region_name":"7","id":"rs909060399","source":"dbSNP","start":140465981,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140465981,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1794753963","clinical_significance":[],"alleles":["G","C"],"end":140465985,"strand":1,"feature_type":"variation","start":140465985,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1794754027","clinical_significance":[],"alleles":["C","A"],"end":140465988,"strand":1,"feature_type":"variation","start":140465988,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140465989,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465989,"clinical_significance":[],"seq_region_name":"7","id":"rs780805030"},{"alleles":["G","A"],"end":140465990,"feature_type":"variation","strand":1,"source":"dbSNP","start":140465990,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs922908112"},{"alleles":["G","T"],"end":140465991,"feature_type":"variation","strand":1,"source":"dbSNP","start":140465991,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794754181"},{"source":"dbSNP","start":140465992,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140465992,"alleles":["A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130304311"},{"seq_region_name":"7","id":"rs1794754239","clinical_significance":[],"start":140465992,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140465994,"alleles":["AAT","AATAAT"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140465994,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140465994,"clinical_significance":[],"seq_region_name":"7","id":"rs933099578"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1050627351","source":"dbSNP","start":140465995,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140465995,"alleles":["C","T"],"feature_type":"variation","strand":1},{"id":"rs888851773","seq_region_name":"7","clinical_significance":[],"start":140465996,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140465996,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"alleles":["T","C","G"],"end":140465998,"feature_type":"variation","strand":1,"source":"dbSNP","start":140465998,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794754462"},{"seq_region_name":"7","id":"rs1439971583","clinical_significance":[],"start":140466004,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140466004,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1011453223","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466006,"feature_type":"variation","strand":1,"end":140466006,"alleles":["A","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs901801480","end":140466007,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140466007,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1377937221","clinical_significance":[],"strand":1,"feature_type":"variation","end":140466010,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466010,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466012,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140466012,"clinical_significance":[],"seq_region_name":"7","id":"rs1225625761"},{"clinical_significance":[],"id":"rs1042903653","seq_region_name":"7","alleles":["G","A"],"end":140466013,"feature_type":"variation","strand":1,"source":"dbSNP","start":140466013,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794754881","feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140466016,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466016},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794754958","feature_type":"variation","strand":1,"end":140466017,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466017},{"seq_region_name":"7","id":"rs1794755056","clinical_significance":[],"end":140466018,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140466018,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466022,"source":"dbSNP","strand":1,"feature_type":"variation","end":140466022,"alleles":["A","C"],"seq_region_name":"7","id":"rs1794755117","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140466023,"alleles":["T","C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466023,"clinical_significance":[],"id":"rs148889998","seq_region_name":"7"},{"end":140466024,"alleles":["TT","TTT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140466023,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs543853277"},{"id":"rs1794755426","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140466024,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466024,"source":"dbSNP"},{"source":"dbSNP","start":140466024,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140466025,"alleles":["TG","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794755522"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1473422320","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466029,"feature_type":"variation","strand":1,"end":140466029,"alleles":["C","G","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794755703","feature_type":"variation","strand":1,"end":140466030,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466030},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794755792","feature_type":"variation","strand":1,"end":140466031,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466031},{"strand":1,"feature_type":"variation","end":140466034,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466034,"source":"dbSNP","seq_region_name":"7","id":"rs1275652660","clinical_significance":[]},{"alleles":["C","A"],"end":140466035,"strand":1,"feature_type":"variation","start":140466035,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs889095217","clinical_significance":[]},{"clinical_significance":[],"id":"rs1794756064","seq_region_name":"7","source":"dbSNP","start":140466036,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140466036,"alleles":["A","C"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140466037,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466037,"source":"dbSNP","seq_region_name":"7","id":"rs1794756150","clinical_significance":[]},{"source":"dbSNP","start":140466037,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","-"],"end":140466037,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794756224"},{"start":140466038,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140466038,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs756931108","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466043,"feature_type":"variation","strand":1,"end":140466043,"alleles":["T","A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1305939957"},{"seq_region_name":"7","id":"rs1794756492","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466049,"source":"dbSNP","strand":1,"feature_type":"variation","end":140466049,"alleles":["C","G"]},{"seq_region_name":"7","id":"rs1794756549","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466053,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140466053},{"start":140466056,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140466056,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794756612","clinical_significance":[]},{"source":"dbSNP","start":140466059,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140466059,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1031025651","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1294022081","alleles":["GACAGAGCGAGAC","GAC"],"end":140466071,"feature_type":"variation","strand":1,"source":"dbSNP","start":140466059,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140466061,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466061,"source":"dbSNP","id":"rs143607620","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1285163385","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466062,"feature_type":"variation","strand":1,"alleles":["AGAG","AG"],"end":140466065},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466064,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140466064,"id":"rs1794756902","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140466066,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140466066,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs181554815"},{"end":140466067,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140466067,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1024179147"},{"feature_type":"variation","strand":1,"end":140466071,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466071,"clinical_significance":[],"seq_region_name":"7","id":"rs1794757252"},{"seq_region_name":"7","id":"rs969492678","clinical_significance":[],"start":140466075,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140466075,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"end":140466079,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140466079,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1347878867"},{"source":"dbSNP","start":140466080,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AAAAAAAA","AAAAAAAAA"],"end":140466087,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs747067866"},{"seq_region_name":"7","id":"rs1292295076","clinical_significance":[],"start":140466081,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140466081,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794757711","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466086,"feature_type":"variation","strand":1,"end":140466090,"alleles":["AACAA","AA"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1175078719","alleles":["A","C"],"end":140466087,"feature_type":"variation","strand":1,"source":"dbSNP","start":140466087,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1794757815","seq_region_name":"7","source":"dbSNP","start":140466088,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140466088,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466089,"feature_type":"variation","strand":1,"alleles":["AAAAAAA","AAAAA","AAAAAA","AAAAAAAA"],"end":140466095,"clinical_significance":[],"seq_region_name":"7","id":"rs1348817002"},{"seq_region_name":"7","id":"rs1406754750","clinical_significance":[],"strand":1,"feature_type":"variation","end":140466091,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466091,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794758027","end":140466092,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140466092,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs980949882","feature_type":"variation","strand":1,"end":140466094,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466094},{"seq_region_name":"7","id":"rs1794758144","clinical_significance":[],"end":140466101,"alleles":["AAGATAAG","AAG"],"strand":1,"feature_type":"variation","start":140466094,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1794758199","clinical_significance":[],"strand":1,"feature_type":"variation","end":140466096,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466096,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1409478623","source":"dbSNP","start":140466098,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140466098,"alleles":["T","A","C"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140466098,"alleles":["T","TT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466098,"clinical_significance":[],"id":"rs1794758355","seq_region_name":"7"},{"seq_region_name":"7","id":"rs2130305169","clinical_significance":[],"start":140466100,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140466100,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466101,"feature_type":"variation","strand":1,"end":140466101,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs984934938"},{"seq_region_name":"7","id":"rs1016349855","clinical_significance":[],"start":140466102,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140466102,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466113,"feature_type":"variation","strand":1,"end":140466113,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794758573"},{"feature_type":"variation","strand":1,"end":140466115,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466115,"clinical_significance":[],"seq_region_name":"7","id":"rs1794758616"},{"seq_region_name":"7","id":"rs1585480397","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466118,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["ATCAT","AT"],"end":140466122},{"end":140466122,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140466122,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1794758733","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1269289233","feature_type":"variation","strand":1,"end":140466124,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466124},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466125,"feature_type":"variation","strand":1,"end":140466125,"alleles":["T","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794758854"},{"seq_region_name":"7","id":"rs1794758904","clinical_significance":[],"strand":1,"feature_type":"variation","end":140466127,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466127,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1585480414","clinical_significance":[],"start":140466131,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140466131,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140466132,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466132,"clinical_significance":[],"seq_region_name":"7","id":"rs572418638"},{"strand":1,"feature_type":"variation","end":140466141,"alleles":["CAAGCA","CA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466136,"source":"dbSNP","id":"rs1794759055","seq_region_name":"7","clinical_significance":[]},{"start":140466137,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140466137,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs962289962","clinical_significance":[]},{"end":140466139,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140466139,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1563092352","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140466146,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466146,"clinical_significance":[],"seq_region_name":"7","id":"rs547064911"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140466147,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466147,"clinical_significance":[],"seq_region_name":"7","id":"rs1415673020"},{"source":"dbSNP","start":140466148,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140466148,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs151033858"},{"seq_region_name":"7","id":"rs933002772","clinical_significance":[],"start":140466149,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140466149,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1309010610","clinical_significance":[],"start":140466150,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140466150,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140466153,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466153,"clinical_significance":[],"seq_region_name":"7","id":"rs1794759471"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466155,"feature_type":"variation","strand":1,"alleles":["C","A","G"],"end":140466155,"clinical_significance":[],"id":"rs1585480466","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1794759597","clinical_significance":[],"end":140466156,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140466156,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140466161,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TTT","T","TT"],"end":140466163,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1327417331","clinical_significance":[]},{"seq_region_name":"7","id":"rs1267760127","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466163,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140466163},{"clinical_significance":[],"id":"rs985809503","seq_region_name":"7","feature_type":"variation","strand":1,"end":140466166,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466166},{"clinical_significance":[],"seq_region_name":"7","id":"rs910325204","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466168,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140466168},{"source":"dbSNP","start":140466169,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TCT","T"],"end":140466171,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1224436618"},{"seq_region_name":"7","id":"rs1794759944","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466171,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140466171},{"start":140466177,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140466177,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794760011","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["TAGCTAG","TAG"],"end":140466183,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466177,"clinical_significance":[],"id":"rs1326140832","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1299758371","clinical_significance":[],"strand":1,"feature_type":"variation","end":140466181,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466181,"source":"dbSNP"},{"id":"rs1386755045","seq_region_name":"7","clinical_significance":[],"start":140466184,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140466184,"strand":1,"feature_type":"variation"},{"start":140466185,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140466185,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1563092384","clinical_significance":[]},{"seq_region_name":"7","id":"rs112642535","clinical_significance":[],"strand":1,"feature_type":"variation","end":140466186,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466186,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140466194,"alleles":["CAATCAA","CAA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466188,"clinical_significance":[],"id":"rs1794760388","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794760455","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466190,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140466190},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794760519","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466194,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140466194},{"seq_region_name":"7","id":"rs771605436","clinical_significance":[],"start":140466195,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140466195,"strand":1,"feature_type":"variation"},{"alleles":["A","G"],"end":140466202,"feature_type":"variation","strand":1,"source":"dbSNP","start":140466202,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1402137432"},{"seq_region_name":"7","id":"rs1794760702","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466206,"source":"dbSNP","strand":1,"feature_type":"variation","end":140466206,"alleles":["T","C"]},{"end":140466208,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140466208,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1319474198"},{"strand":1,"feature_type":"variation","end":140466209,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466209,"source":"dbSNP","seq_region_name":"7","id":"rs1585480541","clinical_significance":[]},{"alleles":["C","T"],"end":140466210,"feature_type":"variation","strand":1,"source":"dbSNP","start":140466210,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794760855"},{"seq_region_name":"7","id":"rs1794760907","clinical_significance":[],"end":140466211,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140466211,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466212,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140466212,"clinical_significance":[],"id":"rs923068805","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140466213,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466213,"clinical_significance":[],"id":"rs1794761031","seq_region_name":"7"},{"seq_region_name":"7","id":"rs902994117","clinical_significance":[],"alleles":["C","T"],"end":140466220,"strand":1,"feature_type":"variation","start":140466220,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs542750795","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466221,"source":"dbSNP","strand":1,"feature_type":"variation","end":140466221,"alleles":["T","G"]},{"start":140466225,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140466225,"strand":1,"feature_type":"variation","id":"rs1794761216","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1432591458","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466226,"feature_type":"variation","strand":1,"end":140466226,"alleles":["T","C","G"]},{"seq_region_name":"7","id":"rs1420303251","clinical_significance":[],"start":140466228,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140466228,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1190529745","clinical_significance":[],"start":140466230,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140466230,"alleles":["C","A","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1247600668","clinical_significance":[],"end":140466231,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140466231,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140466232,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140466232,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794761541","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794761600","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140466233,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466233,"source":"dbSNP"},{"alleles":["T","C"],"end":140466234,"feature_type":"variation","strand":1,"source":"dbSNP","start":140466234,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1484429193"},{"id":"rs1204572875","seq_region_name":"7","clinical_significance":[],"start":140466234,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TAT","TATAT"],"end":140466236,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs569324453","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466236,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140466236},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466239,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140466239,"clinical_significance":[],"seq_region_name":"7","id":"rs1794761816"},{"id":"rs1794761868","seq_region_name":"7","clinical_significance":[],"start":140466242,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140466242,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1794761925","clinical_significance":[],"start":140466248,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140466248,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466248,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CAAGTAGACTAC","C"],"end":140466259,"seq_region_name":"7","id":"rs1233153762","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794762040","source":"dbSNP","start":140466250,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140466250,"feature_type":"variation","strand":1},{"alleles":["G","A","C"],"end":140466251,"strand":1,"feature_type":"variation","start":140466251,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs747455384","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140466254,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466254,"source":"dbSNP","seq_region_name":"7","id":"rs1308660651","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466255,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["ACTACTA","ACTA"],"end":140466261,"seq_region_name":"7","id":"rs1300459671","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140466257,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466257,"source":"dbSNP","seq_region_name":"7","id":"rs536878632","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140466258,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466258,"clinical_significance":[],"seq_region_name":"7","id":"rs1229879784"},{"id":"rs1362436125","seq_region_name":"7","clinical_significance":[],"start":140466261,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140466261,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1229016814","source":"dbSNP","start":140466262,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140466262,"alleles":["T","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1319407297","clinical_significance":[],"alleles":["A","C"],"end":140466263,"strand":1,"feature_type":"variation","start":140466263,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466265,"source":"dbSNP","strand":1,"feature_type":"variation","end":140466265,"alleles":["T","C"],"seq_region_name":"7","id":"rs1794762540","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794762592","clinical_significance":[],"end":140466267,"alleles":["TTT","TT"],"strand":1,"feature_type":"variation","start":140466265,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140466267,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140466267,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794762634"},{"end":140466268,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140466268,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794762680"},{"seq_region_name":"7","id":"rs1794762737","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466269,"source":"dbSNP","strand":1,"feature_type":"variation","end":140466269,"alleles":["T","C"]},{"clinical_significance":[],"id":"rs1057426796","seq_region_name":"7","end":140466273,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140466273,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1794762852","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140466274,"strand":1,"feature_type":"variation","start":140466274,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140466281,"alleles":["TTCCTTTC","TTC"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140466274,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1794762907","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1794762967","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466275,"source":"dbSNP","strand":1,"feature_type":"variation","end":140466275,"alleles":["T","C"]},{"start":140466276,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140466276,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1563092422","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466278,"feature_type":"variation","strand":1,"end":140466278,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794763076"},{"seq_region_name":"7","id":"rs1794763135","clinical_significance":[],"strand":1,"feature_type":"variation","end":140466281,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466281,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140466282,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466282,"clinical_significance":[],"seq_region_name":"7","id":"rs1333339353"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466288,"source":"dbSNP","strand":1,"feature_type":"variation","end":140466288,"alleles":["T","C"],"id":"rs1404085372","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794763318","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466292,"feature_type":"variation","strand":1,"end":140466293,"alleles":["AA","-"]},{"seq_region_name":"7","id":"rs1794763375","clinical_significance":[],"alleles":["G","GTG"],"end":140466296,"strand":1,"feature_type":"variation","start":140466296,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1794763447","clinical_significance":[],"start":140466298,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140466298,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140466299,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466299,"source":"dbSNP","seq_region_name":"7","id":"rs1794763495","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794763547","source":"dbSNP","start":140466300,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140466300,"alleles":["T","C"],"feature_type":"variation","strand":1},{"id":"rs936689170","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140466306,"strand":1,"feature_type":"variation","start":140466306,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794763682","source":"dbSNP","start":140466308,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140466308,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466309,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140466309,"clinical_significance":[],"seq_region_name":"7","id":"rs1794763738"},{"seq_region_name":"7","id":"rs1465372829","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466314,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140466314},{"strand":1,"feature_type":"variation","end":140466320,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466320,"source":"dbSNP","seq_region_name":"7","id":"rs1794763840","clinical_significance":[]},{"seq_region_name":"7","id":"rs1354972568","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140466324,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466324,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1170449722","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140466328,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466328,"source":"dbSNP"},{"id":"rs555155743","seq_region_name":"7","clinical_significance":[],"end":140466330,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","start":140466330,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466332,"feature_type":"variation","strand":1,"end":140466332,"alleles":["A","ATTTA"],"clinical_significance":[],"seq_region_name":"7","id":"rs1389684860"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1184407724","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140466333,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466333},{"seq_region_name":"7","id":"rs892585555","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466335,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140466335},{"end":140466336,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140466336,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1259148710"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466339,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140466339,"clinical_significance":[],"seq_region_name":"7","id":"rs1794764445"},{"feature_type":"variation","strand":1,"end":140466344,"alleles":["A","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466344,"clinical_significance":[],"id":"rs1014037975","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1794764626","clinical_significance":[],"start":140466346,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140466346,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"end":140466348,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140466348,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1200176990"},{"source":"dbSNP","start":140466349,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140466349,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1023602250"},{"end":140466350,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140466350,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1203657534","seq_region_name":"7","clinical_significance":[]},{"id":"rs1202845048","seq_region_name":"7","clinical_significance":[],"start":140466351,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140466355,"alleles":["AGCTA","AGCTAGCTA"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466352,"source":"dbSNP","strand":1,"feature_type":"variation","end":140466352,"alleles":["G","C"],"seq_region_name":"7","id":"rs1794764956","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794765012","clinical_significance":[],"end":140466356,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140466356,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466358,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140466358,"clinical_significance":[],"seq_region_name":"7","id":"rs1339412070"},{"feature_type":"variation","strand":1,"end":140466359,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466359,"clinical_significance":[],"seq_region_name":"7","id":"rs1794765103"},{"feature_type":"variation","strand":1,"end":140466364,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466364,"clinical_significance":[],"id":"rs1794765155","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466366,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AAAA","AAA"],"end":140466369,"seq_region_name":"7","id":"rs1794765209","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140466379,"alleles":["AAAAGGAAAATTAA","AAAAGGAAAATTAAAAAGGAAAATTAA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466366,"source":"dbSNP","seq_region_name":"7","id":"rs1794765292","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794765382","clinical_significance":[],"end":140466380,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140466380,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1025107216","seq_region_name":"7","feature_type":"variation","strand":1,"end":140466382,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466382},{"strand":1,"feature_type":"variation","end":140466389,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466389,"source":"dbSNP","id":"rs905291348","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466391,"source":"dbSNP","strand":1,"feature_type":"variation","end":140466391,"alleles":["C","A"],"id":"rs1245053780","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","T"],"end":140466392,"feature_type":"variation","strand":1,"source":"dbSNP","start":140466392,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585480797"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1006240402","end":140466393,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140466393,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1794765850","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466394,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140466394},{"end":140466395,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140466395,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1341835984","clinical_significance":[]},{"source":"dbSNP","start":140466396,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140466396,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1310145061"},{"seq_region_name":"7","id":"rs1016402218","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466397,"source":"dbSNP","strand":1,"feature_type":"variation","end":140466397,"alleles":["G","T"]},{"seq_region_name":"7","id":"rs377711325","clinical_significance":[],"alleles":["C","T"],"end":140466398,"strand":1,"feature_type":"variation","start":140466398,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1483370938","clinical_significance":[],"strand":1,"feature_type":"variation","end":140466404,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466404,"source":"dbSNP"},{"end":140466405,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140466405,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794766423","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466408,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140466408,"seq_region_name":"7","id":"rs1794766478","clinical_significance":[]},{"alleles":["G","A","T"],"end":140466409,"feature_type":"variation","strand":1,"source":"dbSNP","start":140466409,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794766543"},{"start":140466411,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140466411,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794766605","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140466412,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466412,"source":"dbSNP","seq_region_name":"7","id":"rs962215810","clinical_significance":[]},{"alleles":["T","C"],"end":140466421,"strand":1,"feature_type":"variation","start":140466421,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs972186752","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794766840","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466423,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140466423},{"clinical_significance":[],"seq_region_name":"7","id":"rs1370023819","feature_type":"variation","strand":1,"end":140466427,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466427},{"seq_region_name":"7","id":"rs1031038992","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466428,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140466428},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794766984","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140466429,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466429},{"clinical_significance":[],"seq_region_name":"7","id":"rs1033915394","alleles":["G","T"],"end":140466433,"feature_type":"variation","strand":1,"source":"dbSNP","start":140466433,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1254700933","seq_region_name":"7","alleles":["G","T"],"end":140466434,"feature_type":"variation","strand":1,"source":"dbSNP","start":140466434,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1794767263","clinical_significance":[],"strand":1,"feature_type":"variation","end":140466436,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466436,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1187142446","feature_type":"variation","strand":1,"end":140466443,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466443},{"seq_region_name":"7","id":"rs1794767429","clinical_significance":[],"strand":1,"feature_type":"variation","end":140466446,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466446,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794767510","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466447,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140466447},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794767572","source":"dbSNP","start":140466453,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140466453,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1419994209","clinical_significance":[],"start":140466454,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140466454,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466455,"feature_type":"variation","strand":1,"end":140466455,"alleles":["G","A"],"clinical_significance":[],"id":"rs1794767732","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1794767812","clinical_significance":[],"start":140466455,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["GGG","GG"],"end":140466457,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140466458,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140466458,"alleles":["A","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1254474024"},{"strand":1,"feature_type":"variation","alleles":["GAGA","GA"],"end":140466466,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466463,"source":"dbSNP","seq_region_name":"7","id":"rs1171249014","clinical_significance":[]},{"seq_region_name":"7","id":"rs952979318","clinical_significance":[],"end":140466465,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140466465,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466467,"feature_type":"variation","strand":1,"end":140466467,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130307337"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1209849069","alleles":["A","G"],"end":140466469,"feature_type":"variation","strand":1,"source":"dbSNP","start":140466469,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140466470,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140466470,"alleles":["A","G"],"strand":1,"feature_type":"variation","id":"rs1357888313","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140466472,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466472,"clinical_significance":[],"id":"rs1263267652","seq_region_name":"7"},{"clinical_significance":[],"id":"rs954973772","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466474,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140466474},{"seq_region_name":"7","id":"rs986208323","clinical_significance":[],"strand":1,"feature_type":"variation","end":140466475,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466475,"source":"dbSNP"},{"alleles":["G","A"],"end":140466476,"strand":1,"feature_type":"variation","start":140466476,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794768518","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs910179022","end":140466480,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140466480,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140466481,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140466481,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794768669","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466482,"feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140466482,"clinical_significance":[],"seq_region_name":"7","id":"rs1169468899"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794768869","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466483,"feature_type":"variation","strand":1,"end":140466483,"alleles":["A","T"]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140466484,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466484,"clinical_significance":[],"seq_region_name":"7","id":"rs769171494"},{"clinical_significance":[],"id":"rs573722916","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140466485,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466485},{"clinical_significance":[],"id":"rs1388549369","seq_region_name":"7","source":"dbSNP","start":140466488,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140466488,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466490,"feature_type":"variation","strand":1,"end":140466490,"alleles":["C","T"],"clinical_significance":[],"id":"rs540619992","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466490,"feature_type":"variation","strand":1,"end":140466493,"alleles":["CCCC","CCC","CCCCC"],"clinical_significance":[],"seq_region_name":"7","id":"rs573344072"},{"seq_region_name":"7","id":"rs1353604061","clinical_significance":[],"end":140466491,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140466491,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs552505202","clinical_significance":[],"start":140466493,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140466493,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140466494,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466494,"source":"dbSNP","seq_region_name":"7","id":"rs1157327086","clinical_significance":[]},{"seq_region_name":"7","id":"rs978477022","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466495,"source":"dbSNP","strand":1,"feature_type":"variation","end":140466495,"alleles":["T","G"]},{"seq_region_name":"7","id":"rs1414216350","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466495,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TCTCT","T"],"end":140466499},{"end":140466496,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140466496,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs924339970","seq_region_name":"7"},{"start":140466499,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140466499,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1472473133","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs971770953","feature_type":"variation","strand":1,"end":140466501,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466501},{"seq_region_name":"7","id":"rs923119784","clinical_significance":[],"start":140466502,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140466502,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["AAACAGAATAAA","AAA"],"end":140466513,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466502,"source":"dbSNP","seq_region_name":"7","id":"rs1201677385","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466505,"source":"dbSNP","strand":1,"feature_type":"variation","end":140466505,"alleles":["C","-"],"seq_region_name":"7","id":"rs954553238","clinical_significance":[]},{"end":140466510,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140466510,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs577227732"},{"start":140466511,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140466511,"alleles":["A","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794770324","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["AAAAAAA","AAAAAA","AAAAAAAA"],"end":140466517,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466511,"clinical_significance":[],"seq_region_name":"7","id":"rs1208865555"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794770537","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466513,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140466513},{"seq_region_name":"7","id":"rs1342074822","clinical_significance":[],"start":140466518,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140466518,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1794770707","clinical_significance":[],"end":140466520,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140466520,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466526,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140466526,"clinical_significance":[],"id":"rs186674713","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1272660598","alleles":["G","A","T"],"end":140466527,"feature_type":"variation","strand":1,"source":"dbSNP","start":140466527,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1275319139","end":140466528,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140466528,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs188973322","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466530,"feature_type":"variation","strand":1,"end":140466530,"alleles":["C","T"]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140466531,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466531,"source":"dbSNP","seq_region_name":"7","id":"rs530595653","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466532,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140466532,"seq_region_name":"7","id":"rs948627978","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1045493086","alleles":["G","A"],"end":140466533,"feature_type":"variation","strand":1,"source":"dbSNP","start":140466533,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794771295","end":140466535,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140466535,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140466537,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140466537,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1585481075","seq_region_name":"7"},{"end":140466538,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140466538,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs905175298","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140466542,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466542,"clinical_significance":[],"seq_region_name":"7","id":"rs1006166524"},{"start":140466543,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140466543,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1193728888","clinical_significance":[]},{"alleles":["A","G"],"end":140466549,"strand":1,"feature_type":"variation","start":140466549,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794771593","clinical_significance":[]},{"end":140466550,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140466550,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1037772517","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs910495080","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466552,"feature_type":"variation","strand":1,"end":140466554,"alleles":["CCC","CC"]},{"seq_region_name":"7","id":"rs897908989","clinical_significance":[],"start":140466553,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140466553,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1794771795","seq_region_name":"7","end":140466554,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140466554,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466555,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140466555,"clinical_significance":[],"seq_region_name":"7","id":"rs994104678"},{"clinical_significance":[],"id":"rs1425532271","seq_region_name":"7","source":"dbSNP","start":140466556,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140466556,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466563,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140466563,"clinical_significance":[],"seq_region_name":"7","id":"rs1197477925"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1435592838","feature_type":"variation","strand":1,"end":140466565,"alleles":["GGG","GG"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466563},{"clinical_significance":[],"id":"rs1794771984","seq_region_name":"7","source":"dbSNP","start":140466566,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140466566,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466568,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140466568,"clinical_significance":[],"seq_region_name":"7","id":"rs542840367"},{"seq_region_name":"7","id":"rs1794772090","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140466569,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466569,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140466570,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466570,"source":"dbSNP","id":"rs181637627","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140466571,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466571,"clinical_significance":[],"seq_region_name":"7","id":"rs1434252472"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1007785638","source":"dbSNP","start":140466575,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140466575,"alleles":["C","T"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466576,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140466576,"seq_region_name":"7","id":"rs1464253027","clinical_significance":[]},{"start":140466578,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140466578,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1017293554","clinical_significance":[]},{"clinical_significance":[],"id":"rs952050457","seq_region_name":"7","alleles":["T","C","G"],"end":140466579,"feature_type":"variation","strand":1,"source":"dbSNP","start":140466579,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1794772486","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466581,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140466581},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466583,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140466583,"clinical_significance":[],"seq_region_name":"7","id":"rs1794772547"},{"alleles":["T","C"],"end":140466586,"strand":1,"feature_type":"variation","start":140466586,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs968400539","clinical_significance":[]},{"start":140466587,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140466587,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs1794772655","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466589,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140466589,"clinical_significance":[],"seq_region_name":"7","id":"rs1794772713"},{"seq_region_name":"7","id":"rs528541189","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466590,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140466590},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794772821","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140466594,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466594},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140466597,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466597,"clinical_significance":[],"seq_region_name":"7","id":"rs1274192329"},{"end":140466600,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140466600,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794772867","clinical_significance":[]},{"seq_region_name":"7","id":"rs1429166161","clinical_significance":[],"start":140466601,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140466601,"strand":1,"feature_type":"variation"},{"alleles":["A","G"],"end":140466602,"feature_type":"variation","strand":1,"source":"dbSNP","start":140466602,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794772962"},{"seq_region_name":"7","id":"rs1794772999","clinical_significance":[],"alleles":["A","G"],"end":140466607,"strand":1,"feature_type":"variation","start":140466607,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140466610,"alleles":["CC","C"],"strand":1,"feature_type":"variation","start":140466609,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1794773053","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1794773130","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140466611,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466611},{"source":"dbSNP","start":140466614,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140466614,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1270004538","seq_region_name":"7"},{"start":140466615,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140466615,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1046441217","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs924391839","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140466620,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466620},{"seq_region_name":"7","id":"rs1794773509","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466621,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140466621},{"clinical_significance":[],"seq_region_name":"7","id":"rs1360106408","source":"dbSNP","start":140466622,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140466622,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1336620974","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140466624,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466624},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794773756","alleles":["C","A"],"end":140466628,"feature_type":"variation","strand":1,"source":"dbSNP","start":140466628,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1794773832","clinical_significance":[],"strand":1,"feature_type":"variation","end":140466630,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466630,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1829771","clinical_significance":[],"end":140466631,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140466631,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140466632,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140466632,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585481278","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466634,"source":"dbSNP","strand":1,"feature_type":"variation","end":140466640,"alleles":["CTCTACT","CT"],"seq_region_name":"7","id":"rs1794774107","clinical_significance":[]},{"clinical_significance":[],"id":"rs1794774195","seq_region_name":"7","feature_type":"variation","strand":1,"end":140466635,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466635},{"seq_region_name":"7","id":"rs10259468","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466636,"source":"dbSNP","strand":1,"feature_type":"variation","end":140466636,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585481290","alleles":["T","C"],"end":140466637,"feature_type":"variation","strand":1,"source":"dbSNP","start":140466637,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1253212149","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466640,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140466640},{"end":140466644,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140466644,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1794774528","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1002354512","feature_type":"variation","strand":1,"alleles":["A","T"],"end":140466645,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466645},{"seq_region_name":"7","id":"rs1794774711","clinical_significance":[],"strand":1,"feature_type":"variation","end":140466654,"alleles":["AAAAAA","AAAAAAA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466649,"source":"dbSNP"},{"id":"rs1169817175","seq_region_name":"7","clinical_significance":[],"alleles":["A","C"],"end":140466652,"strand":1,"feature_type":"variation","start":140466652,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1449488012","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466653,"source":"dbSNP","strand":1,"feature_type":"variation","end":140466653,"alleles":["A","C"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466654,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["-","T"],"end":140466653,"seq_region_name":"7","id":"rs1794774967","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140466654,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466654,"source":"dbSNP","seq_region_name":"7","id":"rs1794775050","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466655,"feature_type":"variation","strand":1,"end":140466655,"alleles":["T","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794775122"},{"clinical_significance":[],"id":"rs993073254","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140466660,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466660},{"seq_region_name":"7","id":"rs1391529998","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466660,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CGGGCGCGGTGGCGGGCGC","CGGGCGC"],"end":140466678},{"clinical_significance":[],"seq_region_name":"7","id":"rs571637281","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466661,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140466661},{"source":"dbSNP","start":140466662,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140466662,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs888733113"},{"id":"rs1346685506","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140466664,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466664,"source":"dbSNP"},{"start":140466665,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140466665,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs948660839","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1285661625","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466666,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140466666},{"alleles":["G","A","C"],"end":140466667,"feature_type":"variation","strand":1,"source":"dbSNP","start":140466667,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs532572528"},{"seq_region_name":"7","id":"rs1214921863","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466669,"source":"dbSNP","strand":1,"feature_type":"variation","end":140466669,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1794776544","clinical_significance":[],"strand":1,"feature_type":"variation","end":140466670,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466670,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1247096632","clinical_significance":[],"end":140466672,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140466672,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs551275219","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140466673,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466673},{"seq_region_name":"7","id":"rs1191506360","clinical_significance":[],"start":140466676,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140466676,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466677,"source":"dbSNP","strand":1,"feature_type":"variation","end":140466677,"alleles":["G","A"],"seq_region_name":"7","id":"rs1446223022","clinical_significance":[]},{"alleles":["T","C"],"end":140466680,"strand":1,"feature_type":"variation","start":140466680,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1393580198","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140466681,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466681,"source":"dbSNP","seq_region_name":"7","id":"rs1309143702","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466682,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140466682,"clinical_significance":[],"seq_region_name":"7","id":"rs1794777097"},{"seq_region_name":"7","id":"rs942073843","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466684,"source":"dbSNP","strand":1,"feature_type":"variation","end":140466684,"alleles":["G","A","C"]},{"feature_type":"variation","strand":1,"end":140466687,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466687,"clinical_significance":[],"seq_region_name":"7","id":"rs1794777292"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466690,"feature_type":"variation","strand":1,"end":140466690,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs983395191"},{"clinical_significance":[],"id":"rs1794777438","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466691,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140466691},{"clinical_significance":[],"seq_region_name":"7","id":"rs1432209509","alleles":["C","A"],"end":140466694,"feature_type":"variation","strand":1,"source":"dbSNP","start":140466694,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs961684626","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140466696,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466696},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466697,"feature_type":"variation","strand":1,"end":140466697,"alleles":["G","A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1453939753"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794777817","end":140466701,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140466701,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1642646689","seq_region_name":"7","source":"dbSNP","start":140466705,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140466705,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466706,"source":"dbSNP","strand":1,"feature_type":"variation","end":140466706,"alleles":["A","G"],"seq_region_name":"7","id":"rs993146688","clinical_significance":[]},{"clinical_significance":[],"id":"rs1159234532","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466707,"feature_type":"variation","strand":1,"end":140466707,"alleles":["G","C"]},{"alleles":["G","A","T"],"end":140466712,"strand":1,"feature_type":"variation","start":140466712,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1387171030","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794778107","clinical_significance":[],"end":140466714,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140466714,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1037656469","seq_region_name":"7","clinical_significance":[],"start":140466718,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C"],"end":140466718,"strand":1,"feature_type":"variation"},{"start":140466720,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140466720,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794778220","clinical_significance":[]},{"clinical_significance":[],"id":"rs897918813","seq_region_name":"7","end":140466721,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140466721,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466722,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","G"],"end":140466722,"id":"rs1585481460","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794778419","clinical_significance":[],"alleles":["A","C","T"],"end":140466725,"strand":1,"feature_type":"variation","start":140466725,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["C","T"],"end":140466726,"strand":1,"feature_type":"variation","start":140466726,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585481468","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs186297292","source":"dbSNP","start":140466727,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140466727,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140466728,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140466728,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs954437705","seq_region_name":"7"},{"alleles":["G","C"],"end":140466729,"feature_type":"variation","strand":1,"source":"dbSNP","start":140466729,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794778741"},{"seq_region_name":"7","id":"rs986002297","clinical_significance":[],"end":140466731,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140466731,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794778831","feature_type":"variation","strand":1,"end":140466732,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466732},{"alleles":["A","G"],"end":140466733,"feature_type":"variation","strand":1,"source":"dbSNP","start":140466733,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1484029366"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585481500","source":"dbSNP","start":140466734,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140466734,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs993556430","clinical_significance":[],"start":140466735,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140466735,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"start":140466736,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140466736,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1052382367","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140466738,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466738,"source":"dbSNP","seq_region_name":"7","id":"rs1794779061","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794779117","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466744,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140466744},{"feature_type":"variation","strand":1,"end":140466745,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466745,"clinical_significance":[],"seq_region_name":"7","id":"rs1204438699"},{"id":"rs1794779239","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466746,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140466746},{"seq_region_name":"7","id":"rs375134472","clinical_significance":[],"alleles":["A","G"],"end":140466748,"strand":1,"feature_type":"variation","start":140466748,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1008126709","clinical_significance":[],"start":140466749,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140466749,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1794779411","clinical_significance":[],"start":140466750,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140466750,"alleles":["G","A","C"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466752,"feature_type":"variation","strand":1,"end":140466752,"alleles":["C","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1017910586"},{"source":"dbSNP","start":140466753,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140466753,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1240343687","seq_region_name":"7"},{"alleles":["G","A"],"end":140466755,"feature_type":"variation","strand":1,"source":"dbSNP","start":140466755,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs910347447"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466756,"feature_type":"variation","strand":1,"end":140466756,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794779657"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1289441005","end":140466757,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140466757,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1412203123","seq_region_name":"7","source":"dbSNP","start":140466758,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140466758,"feature_type":"variation","strand":1},{"start":140466759,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140466759,"alleles":["G","T"],"strand":1,"feature_type":"variation","id":"rs968952924","seq_region_name":"7","clinical_significance":[]},{"end":140466760,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140466760,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs999870911","clinical_significance":[]},{"seq_region_name":"7","id":"rs1031303050","clinical_significance":[],"start":140466761,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140466761,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466762,"source":"dbSNP","strand":1,"feature_type":"variation","end":140466762,"alleles":["C","G","T"],"seq_region_name":"7","id":"rs1794780932","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140466763,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466763,"source":"dbSNP","seq_region_name":"7","id":"rs1794780981","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140466768,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466768,"clinical_significance":[],"seq_region_name":"7","id":"rs1222687688"},{"feature_type":"variation","strand":1,"end":140466770,"alleles":["G","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466770,"clinical_significance":[],"seq_region_name":"7","id":"rs1794781310"},{"seq_region_name":"7","id":"rs956003627","clinical_significance":[],"strand":1,"feature_type":"variation","end":140466773,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466773,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466774,"feature_type":"variation","strand":1,"end":140466774,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs543822592"},{"id":"rs1211598247","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466776,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140466776},{"seq_region_name":"7","id":"rs1416883049","clinical_significance":[],"alleles":["G","A"],"end":140466777,"strand":1,"feature_type":"variation","start":140466777,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs562607067","clinical_significance":[],"strand":1,"feature_type":"variation","end":140466780,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466780,"source":"dbSNP"},{"clinical_significance":[],"id":"rs969942381","seq_region_name":"7","alleles":["G","A"],"end":140466781,"feature_type":"variation","strand":1,"source":"dbSNP","start":140466781,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1249478319","seq_region_name":"7","source":"dbSNP","start":140466782,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140466782,"alleles":["G","A"],"feature_type":"variation","strand":1},{"start":140466785,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140466785,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1176573650","clinical_significance":[]},{"source":"dbSNP","start":140466786,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140466786,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794781842"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1488835277","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466788,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140466788},{"clinical_significance":[],"seq_region_name":"7","id":"rs1468222699","alleles":["C","A","T"],"end":140466789,"feature_type":"variation","strand":1,"source":"dbSNP","start":140466789,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140466790,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466790,"clinical_significance":[],"seq_region_name":"7","id":"rs980338923"},{"start":140466795,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140466795,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1365727595","clinical_significance":[]},{"start":140466796,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140466796,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs1794782221","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140466797,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466797,"source":"dbSNP","seq_region_name":"7","id":"rs577638369","clinical_significance":[]},{"source":"dbSNP","start":140466798,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140466798,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1468710683","seq_region_name":"7"},{"id":"rs1288251065","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C","T"],"end":140466799,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466799,"source":"dbSNP"},{"seq_region_name":"7","id":"rs2130309590","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466800,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140466800},{"feature_type":"variation","strand":1,"end":140466803,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466803,"clinical_significance":[],"seq_region_name":"7","id":"rs1585481674"},{"end":140466805,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140466805,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794782509","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140466806,"alleles":["G","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466806,"clinical_significance":[],"id":"rs1158052783","seq_region_name":"7"},{"start":140466807,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140466807,"alleles":["T","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794782726","clinical_significance":[]},{"alleles":["TCTC","TC"],"end":140466810,"strand":1,"feature_type":"variation","start":140466807,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794782811","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794782887","clinical_significance":[],"start":140466808,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140466808,"alleles":["C","A","T"],"strand":1,"feature_type":"variation"},{"start":140466809,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140466809,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1367689963","clinical_significance":[]},{"clinical_significance":[],"id":"rs1794783062","seq_region_name":"7","feature_type":"variation","strand":1,"end":140466809,"alleles":["T","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466809},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466809,"feature_type":"variation","strand":1,"alleles":["TCA","-"],"end":140466811,"clinical_significance":[],"seq_region_name":"7","id":"rs1794783138"},{"end":140466809,"alleles":["-","A","AA","AAA"],"strand":1,"feature_type":"variation","start":140466810,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1794783228","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1186275340","clinical_significance":[],"strand":1,"feature_type":"variation","end":140466810,"alleles":["C","A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466810,"source":"dbSNP"},{"start":140466810,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","-"],"end":140466810,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1294837423","clinical_significance":[]},{"alleles":["CA","-"],"end":140466811,"strand":1,"feature_type":"variation","start":140466810,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1794783565","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466810,"feature_type":"variation","strand":1,"alleles":["CAA","-"],"end":140466812,"clinical_significance":[],"seq_region_name":"7","id":"rs1433693679"},{"clinical_significance":[],"id":"rs1393191769","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466810,"feature_type":"variation","strand":1,"alleles":["CAAA","-"],"end":140466813},{"seq_region_name":"7","id":"rs1419292435","clinical_significance":[],"strand":1,"feature_type":"variation","end":140466821,"alleles":["CAAAAAAAAAAA","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466810,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1794783905","clinical_significance":[],"start":140466811,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140466811,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140466811,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AAAAAAAAAAAAAAAAAAAAAAA","AAAAAAA","AAAAAAAAA","AAAAAAAAAA","AAAAAAAAAAA","AAAAAAAAAAAA","AAAAAAAAAAAAA","AAAAAAAAAAAAAA","AAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA"],"end":140466833,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs563645827"},{"source":"dbSNP","start":140466814,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["-","G"],"end":140466813,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1288127320"},{"id":"rs1794785061","seq_region_name":"7","clinical_significance":[],"start":140466814,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140466814,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1794785128","seq_region_name":"7","alleles":["A","ACA"],"end":140466814,"feature_type":"variation","strand":1,"source":"dbSNP","start":140466814,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140466815,"alleles":["-","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140466816,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1466370131"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585481816","alleles":["A","G"],"end":140466818,"feature_type":"variation","strand":1,"source":"dbSNP","start":140466818,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140466821,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140466821,"alleles":["A","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585481829"},{"end":140466822,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","start":140466822,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs909835305","clinical_significance":[]},{"clinical_significance":[],"id":"rs1173898186","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466823,"feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140466823},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140466824,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466824,"clinical_significance":[],"id":"rs941245542","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140466825,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466825,"clinical_significance":[],"seq_region_name":"7","id":"rs867446070"},{"source":"dbSNP","start":140466826,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G","T"],"end":140466826,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1261315099"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466826,"source":"dbSNP","strand":1,"feature_type":"variation","end":140466836,"alleles":["AAAAAAAAGAA","AA"],"seq_region_name":"7","id":"rs2130310084","clinical_significance":[]},{"seq_region_name":"7","id":"rs1190753451","clinical_significance":[],"start":140466826,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AAAAAAAAGAATAAAAAAA","AAAAAAA"],"end":140466844,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1794786280","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466827,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["-","G"],"end":140466826},{"clinical_significance":[],"seq_region_name":"7","id":"rs1447954605","feature_type":"variation","strand":1,"alleles":["A","AGA"],"end":140466827,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466827},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585481871","feature_type":"variation","strand":1,"alleles":["A","T"],"end":140466827,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466827},{"clinical_significance":[],"id":"rs1055702898","seq_region_name":"7","feature_type":"variation","strand":1,"end":140466828,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466828},{"alleles":["-","G"],"end":140466828,"strand":1,"feature_type":"variation","start":140466829,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1554448651","clinical_significance":[]},{"seq_region_name":"7","id":"rs938092737","clinical_significance":[],"end":140466833,"alleles":["AAAAA","AAAAAAAAAAAAAAAACAAAAA"],"strand":1,"feature_type":"variation","start":140466829,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140466830,"alleles":["A","C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140466830,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs888585780"},{"end":140466832,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140466832,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794786889","clinical_significance":[]},{"clinical_significance":[],"id":"rs369455420","seq_region_name":"7","end":140466834,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140466834,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140466834,"alleles":["G","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466834,"source":"dbSNP","seq_region_name":"7","id":"rs1794787057","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1333610736","feature_type":"variation","strand":1,"alleles":["GAAT","-"],"end":140466837,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466834},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466836,"feature_type":"variation","strand":1,"end":140466836,"alleles":["A","G","T"],"clinical_significance":[],"id":"rs13234915","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs148503395","source":"dbSNP","start":140466837,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140466837,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1231330396","alleles":["A","G"],"end":140466838,"feature_type":"variation","strand":1,"source":"dbSNP","start":140466838,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466838,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AAAAAAA","AAA","AAAAAAAA"],"end":140466844,"seq_region_name":"7","id":"rs1210858105","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1274814511","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466840,"feature_type":"variation","strand":1,"end":140466840,"alleles":["A","G"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466842,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140466842,"seq_region_name":"7","id":"rs1794787690","clinical_significance":[]},{"source":"dbSNP","start":140466843,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140466843,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794787746"},{"strand":1,"feature_type":"variation","end":140466844,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466844,"source":"dbSNP","id":"rs1272354394","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1318390765","seq_region_name":"7","alleles":["C","A"],"end":140466845,"feature_type":"variation","strand":1,"source":"dbSNP","start":140466845,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140466847,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466847,"source":"dbSNP","seq_region_name":"7","id":"rs1252994108","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794788001","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466848,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140466848},{"seq_region_name":"7","id":"rs1037666349","clinical_significance":[],"start":140466849,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140466849,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140466850,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466850,"source":"dbSNP","seq_region_name":"7","id":"rs919235678","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140466851,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466851,"source":"dbSNP","id":"rs1794788154","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1436284493","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466855,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140466855},{"seq_region_name":"7","id":"rs1362504575","clinical_significance":[],"start":140466856,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["GTGGTGGT","GTGGTGGTGTGGTGGT"],"end":140466863,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466857,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140466857,"clinical_significance":[],"seq_region_name":"7","id":"rs1585482001"},{"end":140466858,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140466858,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1006226911","seq_region_name":"7"},{"id":"rs1181175809","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140466859,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466859,"source":"dbSNP"},{"alleles":["T","G"],"end":140466860,"strand":1,"feature_type":"variation","start":140466860,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs2130310513","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140466862,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140466862,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1563092775","seq_region_name":"7"},{"alleles":["C","T"],"end":140466866,"feature_type":"variation","strand":1,"source":"dbSNP","start":140466866,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1037312724","seq_region_name":"7"},{"start":140466867,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140466867,"strand":1,"feature_type":"variation","id":"rs897399826","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466868,"feature_type":"variation","strand":1,"end":140466868,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794788670"},{"feature_type":"variation","strand":1,"end":140466869,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466869,"clinical_significance":[],"seq_region_name":"7","id":"rs1434102501"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794788770","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466873,"feature_type":"variation","strand":1,"end":140466873,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs929394140","clinical_significance":[],"strand":1,"feature_type":"variation","end":140466874,"alleles":["C","A","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466874,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1051884198","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466875,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140466875},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466877,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140466877,"clinical_significance":[],"seq_region_name":"7","id":"rs1794788962"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466880,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140466880,"seq_region_name":"7","id":"rs1794789018","clinical_significance":[]},{"source":"dbSNP","start":140466882,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140466882,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs890517673"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1372682228","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466888,"feature_type":"variation","strand":1,"end":140466888,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1756473567","alleles":["G","A"],"end":140466889,"feature_type":"variation","strand":1,"source":"dbSNP","start":140466889,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs943585420","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466894,"feature_type":"variation","strand":1,"end":140466894,"alleles":["C","G","T"]},{"seq_region_name":"7","id":"rs1425900350","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466896,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140466896},{"alleles":["T","C"],"end":140466900,"strand":1,"feature_type":"variation","start":140466900,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1254560554","clinical_significance":[]},{"clinical_significance":[],"id":"rs954448869","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140466901,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466901},{"seq_region_name":"7","id":"rs1030000853","clinical_significance":[],"start":140466901,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140466916,"alleles":["GGGCAAGAGGGCAAGA","GGGCAAGAGGGCAAGAGGGCAAGA"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1794789482","clinical_significance":[],"strand":1,"feature_type":"variation","end":140466902,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466902,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140466907,"alleles":["GGCAAG","GGCAAGGCAAG"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466902,"clinical_significance":[],"seq_region_name":"7","id":"rs1163351873"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466904,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140466904,"clinical_significance":[],"seq_region_name":"7","id":"rs1039187975"},{"clinical_significance":[],"id":"rs1206591262","seq_region_name":"7","source":"dbSNP","start":140466907,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140466907,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1336913884","clinical_significance":[],"end":140466908,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140466908,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140466910,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140466910,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1250394154","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1417735644","seq_region_name":"7","alleles":["G","A"],"end":140466911,"feature_type":"variation","strand":1,"source":"dbSNP","start":140466911,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140466919,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140466919,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1007277402","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794789940","alleles":["G","A","T"],"end":140466920,"feature_type":"variation","strand":1,"source":"dbSNP","start":140466920,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140466937,"alleles":["AAAACAAAGAAA","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466926,"source":"dbSNP","seq_region_name":"7","id":"rs1794789982","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794790024","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466927,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140466927},{"seq_region_name":"7","id":"rs904778584","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140466930,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466930,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["AAAGAAAGAAA","AAAGAAA"],"end":140466941,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466931,"source":"dbSNP","seq_region_name":"7","id":"rs1794790132","clinical_significance":[]},{"start":140466932,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140466932,"alleles":["A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794790192","clinical_significance":[]},{"id":"rs1794790251","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466933,"source":"dbSNP","strand":1,"feature_type":"variation","end":140466933,"alleles":["A","C"]},{"seq_region_name":"7","id":"rs76893674","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466938,"source":"dbSNP","strand":1,"feature_type":"variation","end":140466938,"alleles":["G","C"]},{"seq_region_name":"7","id":"rs1563092816","clinical_significance":[],"start":140466939,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140466941,"alleles":["AAA","AAAA"],"strand":1,"feature_type":"variation"},{"start":140466939,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140466948,"alleles":["AAACAAACAA","AAACAA","AAACAAACAAACAA"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs201584159","clinical_significance":[]},{"source":"dbSNP","start":140466942,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140466942,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1309812319"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794790545","alleles":["AACAACAA","AACAA"],"end":140466951,"feature_type":"variation","strand":1,"source":"dbSNP","start":140466944,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140466946,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140466946,"alleles":["C","A"],"strand":1,"feature_type":"variation","id":"rs116454670","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs957872837","clinical_significance":[],"start":140466948,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140466948,"alleles":["A","AACCA"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1794790661","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466948,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140466948},{"seq_region_name":"7","id":"rs989700415","clinical_significance":[],"alleles":["AACCAATTAA","AA"],"end":140466960,"strand":1,"feature_type":"variation","start":140466951,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140466955,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140466955,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs891491661"},{"source":"dbSNP","start":140466957,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140466957,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794790931"},{"seq_region_name":"7","id":"rs1794790991","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466958,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140466958},{"id":"rs534374067","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466959,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140466959},{"feature_type":"variation","strand":1,"end":140466961,"alleles":["G","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466961,"clinical_significance":[],"seq_region_name":"7","id":"rs1473124247"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1312987100","end":140466970,"alleles":["TTCCTTTC","TTC"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140466963,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["T","A"],"end":140466964,"feature_type":"variation","strand":1,"source":"dbSNP","start":140466964,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794791246"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585482255","source":"dbSNP","start":140466966,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140466966,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs927927586","alleles":["T","C"],"end":140466968,"feature_type":"variation","strand":1,"source":"dbSNP","start":140466968,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794791393","end":140466971,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140466971,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466972,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140466972,"clinical_significance":[],"seq_region_name":"7","id":"rs1024099900"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466976,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140466976,"seq_region_name":"7","id":"rs1794791501","clinical_significance":[]},{"clinical_significance":[],"id":"rs1249292165","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466976,"feature_type":"variation","strand":1,"alleles":["TTTCTTT","TTT"],"end":140466982},{"alleles":["TTCTT","TT"],"end":140466981,"strand":1,"feature_type":"variation","start":140466977,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1210053650","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs970201792","source":"dbSNP","start":140466979,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140466979,"alleles":["C","T"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140466980,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466980,"clinical_significance":[],"id":"rs1794791719","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs371673846","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466980,"feature_type":"variation","strand":1,"end":140466994,"alleles":["TTTTTTTTTTTTTTT","TTTTT","TTTTTTTT","TTTTTTTTTT","TTTTTTTTTTT","TTTTTTTTTTTT","TTTTTTTTTTTTT","TTTTTTTTTTTTTT","TTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTT"]},{"end":140466981,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","start":140466981,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1292652683","clinical_significance":[]},{"seq_region_name":"7","id":"rs979911783","clinical_significance":[],"alleles":["T","C"],"end":140466982,"strand":1,"feature_type":"variation","start":140466982,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["-","C"],"end":140466982,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466983,"source":"dbSNP","id":"rs1794792005","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs545203482","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466983,"feature_type":"variation","strand":1,"end":140466983,"alleles":["T","A","C"]},{"seq_region_name":"7","id":"rs1325511296","clinical_significance":[],"start":140466984,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140466984,"alleles":["T","TCT"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1458048971","clinical_significance":[],"start":140466984,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140466984,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140466985,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466985,"clinical_significance":[],"seq_region_name":"7","id":"rs1391340969"},{"start":140466988,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140466988,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1157587674","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140466992,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466992,"source":"dbSNP","seq_region_name":"7","id":"rs1794792454","clinical_significance":[]},{"id":"rs1794792523","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140466993,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TTG","-"],"end":140466995},{"start":140466994,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140466994,"strand":1,"feature_type":"variation","id":"rs776772713","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1249332395","seq_region_name":"7","end":140466995,"alleles":["G","C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140466995,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466995,"feature_type":"variation","strand":1,"end":140466995,"alleles":["G","-"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794792848"},{"source":"dbSNP","start":140466996,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140466996,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794792936"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1198871395","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140466997,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140466997},{"start":140466999,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140466999,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1434432212","clinical_significance":[]},{"seq_region_name":"7","id":"rs1337705549","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","AA"],"end":140467000,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467000,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs941569790","alleles":["AGAG","AG"],"end":140467003,"feature_type":"variation","strand":1,"source":"dbSNP","start":140467000,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1794793425","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140467001,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467001,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467002,"feature_type":"variation","strand":1,"end":140467002,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1212733536"},{"id":"rs1465154413","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467003,"source":"dbSNP","strand":1,"feature_type":"variation","end":140467003,"alleles":["G","A","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467007,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140467007,"seq_region_name":"7","id":"rs1269858492","clinical_significance":[]},{"seq_region_name":"7","id":"rs1037601034","clinical_significance":[],"strand":1,"feature_type":"variation","end":140467008,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467008,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794793892","end":140467009,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140467009,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140467013,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467013,"clinical_significance":[],"seq_region_name":"7","id":"rs1349789922"},{"clinical_significance":[],"seq_region_name":"7","id":"rs552665430","feature_type":"variation","strand":1,"end":140467014,"alleles":["G","A","C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467014},{"clinical_significance":[],"seq_region_name":"7","id":"rs918485252","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467037,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140467037},{"clinical_significance":[],"seq_region_name":"7","id":"rs1368896646","source":"dbSNP","start":140467037,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140467056,"alleles":["GTACGATCTTGGCTCACCAC","-"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140467038,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140467038,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1436181993","seq_region_name":"7"},{"alleles":["A","G"],"end":140467039,"strand":1,"feature_type":"variation","start":140467039,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1563092895","clinical_significance":[]},{"clinical_significance":[],"id":"rs1367781353","seq_region_name":"7","source":"dbSNP","start":140467040,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140467040,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467041,"feature_type":"variation","strand":1,"end":140467041,"alleles":["G","A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs560423515"},{"alleles":["T","C"],"end":140467045,"strand":1,"feature_type":"variation","start":140467045,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1051437832","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1403486829","feature_type":"variation","strand":1,"end":140467046,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467046},{"id":"rs2130311628","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140467056,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467056,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1174852486","clinical_significance":[],"start":140467057,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140467057,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794794966","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467061,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140467061},{"seq_region_name":"7","id":"rs1257517645","clinical_significance":[],"start":140467061,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140467069,"alleles":["TCCACCTCC","TCC"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794795156","alleles":["C","T"],"end":140467062,"feature_type":"variation","strand":1,"source":"dbSNP","start":140467062,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs890098084","clinical_significance":[],"strand":1,"feature_type":"variation","end":140467063,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467063,"source":"dbSNP"},{"end":140467064,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140467064,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585482500"},{"seq_region_name":"7","id":"rs1192611373","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140467070,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467070,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467071,"feature_type":"variation","strand":1,"end":140467071,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1007740366"},{"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140467073,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467073,"source":"dbSNP","seq_region_name":"7","id":"rs191039080","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1190672697","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467074,"feature_type":"variation","strand":1,"alleles":["TTCAAGTGATTC","TTC"],"end":140467085},{"end":140467075,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140467075,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794795667","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140467078,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467078,"clinical_significance":[],"seq_region_name":"7","id":"rs1446244253"},{"seq_region_name":"7","id":"rs1429560462","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467080,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140467080},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794795799","end":140467086,"alleles":["T","TT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140467086,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467087,"source":"dbSNP","strand":1,"feature_type":"variation","end":140467087,"alleles":["C","A"],"seq_region_name":"7","id":"rs987869734","clinical_significance":[]},{"end":140467089,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140467089,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794795893"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467091,"feature_type":"variation","strand":1,"end":140467091,"alleles":["C","A"],"clinical_significance":[],"id":"rs1794795949","seq_region_name":"7"},{"id":"rs1794796002","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140467094,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467094,"source":"dbSNP"},{"id":"rs911989778","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467102,"source":"dbSNP","strand":1,"feature_type":"variation","end":140467102,"alleles":["A","G"]},{"end":140467109,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140467109,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1371653710","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467110,"feature_type":"variation","strand":1,"end":140467110,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1461203039"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140467112,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467112,"clinical_significance":[],"seq_region_name":"7","id":"rs943409269"},{"alleles":["G","A"],"end":140467113,"strand":1,"feature_type":"variation","start":140467113,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs893532974","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467120,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140467120,"clinical_significance":[],"seq_region_name":"7","id":"rs1794796349"},{"alleles":["C","A"],"end":140467122,"feature_type":"variation","strand":1,"source":"dbSNP","start":140467122,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1010773188","seq_region_name":"7"},{"seq_region_name":"7","id":"rs376584673","clinical_significance":[],"strand":1,"feature_type":"variation","end":140467124,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467124,"source":"dbSNP"},{"alleles":["C","T"],"end":140467126,"strand":1,"feature_type":"variation","start":140467126,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs904665413","clinical_significance":[]},{"seq_region_name":"7","id":"rs966600299","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467127,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140467127},{"seq_region_name":"7","id":"rs541104440","clinical_significance":[],"start":140467128,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140467128,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140467131,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467131,"source":"dbSNP","seq_region_name":"7","id":"rs1413543427","clinical_significance":[]},{"start":140467132,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140467132,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs981958449","clinical_significance":[]},{"id":"rs1794796970","seq_region_name":"7","clinical_significance":[],"start":140467134,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140467134,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140467136,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467136,"clinical_significance":[],"seq_region_name":"7","id":"rs13438384"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467140,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140467140,"clinical_significance":[],"id":"rs1794797144","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1304505883","seq_region_name":"7","source":"dbSNP","start":140467141,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140467141,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140467143,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467143,"clinical_significance":[],"seq_region_name":"7","id":"rs1350322306"},{"seq_region_name":"7","id":"rs1429832787","clinical_significance":[],"strand":1,"feature_type":"variation","end":140467148,"alleles":["TTTT","TTTTTT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467145,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1208825730","clinical_significance":[],"alleles":["T","C"],"end":140467147,"strand":1,"feature_type":"variation","start":140467147,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467152,"feature_type":"variation","strand":1,"end":140467152,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs770108800"},{"seq_region_name":"7","id":"rs1165813344","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467152,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TTTTT","TTTTTT"],"end":140467156},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467156,"feature_type":"variation","strand":1,"end":140467156,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794797584"},{"clinical_significance":[],"id":"rs959375125","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467157,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140467157},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467159,"feature_type":"variation","strand":1,"end":140467159,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794797699"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1189519541","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467160,"feature_type":"variation","strand":1,"alleles":["AGAGA","AGA"],"end":140467164},{"strand":1,"feature_type":"variation","end":140467163,"alleles":["G","GGG"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467163,"source":"dbSNP","seq_region_name":"7","id":"rs1794797803","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140467165,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467165,"clinical_significance":[],"seq_region_name":"7","id":"rs1484617597"},{"seq_region_name":"7","id":"rs1486492343","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467166,"source":"dbSNP","strand":1,"feature_type":"variation","end":140467166,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs892042393","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140467167,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467167,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1585482716","seq_region_name":"7","alleles":["T","G"],"end":140467170,"feature_type":"variation","strand":1,"source":"dbSNP","start":140467170,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140467173,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467173,"source":"dbSNP","seq_region_name":"7","id":"rs1013953888","clinical_significance":[]},{"start":140467178,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140467178,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs910003476","clinical_significance":[]},{"id":"rs1794798206","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467179,"source":"dbSNP","strand":1,"feature_type":"variation","end":140467179,"alleles":["G","T"]},{"clinical_significance":[],"id":"rs941441219","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140467180,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467180},{"start":140467181,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140467181,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585482740","clinical_significance":[]},{"seq_region_name":"7","id":"rs182554681","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140467184,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467184,"source":"dbSNP"},{"end":140467185,"alleles":["GG","GGG"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140467184,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1443229201"},{"seq_region_name":"7","id":"rs1794798502","clinical_significance":[],"alleles":["G","A"],"end":140467185,"strand":1,"feature_type":"variation","start":140467185,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140467186,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140467186,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1024355619"},{"seq_region_name":"7","id":"rs74555990","clinical_significance":[],"start":140467189,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140467189,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"end":140467192,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140467192,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1260225372","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs549344433","feature_type":"variation","strand":1,"end":140467193,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467193},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794798822","feature_type":"variation","strand":1,"alleles":["AAAT","AAATAAAT"],"end":140467197,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467194},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140467197,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467197,"source":"dbSNP","seq_region_name":"7","id":"rs13438583","clinical_significance":[]},{"source":"dbSNP","start":140467199,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140467199,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794799084"},{"id":"rs1355303233","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467200,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140467200},{"feature_type":"variation","strand":1,"end":140467201,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467201,"clinical_significance":[],"seq_region_name":"7","id":"rs191112351"},{"feature_type":"variation","strand":1,"end":140467202,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467202,"clinical_significance":[],"id":"rs972521013","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs943078398","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467214,"feature_type":"variation","strand":1,"end":140467214,"alleles":["T","C"]},{"clinical_significance":[],"id":"rs1563092996","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467215,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140467215},{"clinical_significance":[],"seq_region_name":"7","id":"rs1025599356","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467217,"feature_type":"variation","strand":1,"end":140467217,"alleles":["T","A"]},{"id":"rs1794799654","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140467218,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467218,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1409071588","source":"dbSNP","start":140467218,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140467219,"alleles":["CC","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1172487174","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467220,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140467220},{"end":140467228,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140467228,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs561470607","clinical_significance":[]},{"end":140467230,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140467230,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1363817440","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1228541671","feature_type":"variation","strand":1,"end":140467234,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467234},{"seq_region_name":"7","id":"rs1455310717","clinical_significance":[],"start":140467237,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140467237,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1794800053","clinical_significance":[],"start":140467238,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140467238,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467240,"feature_type":"variation","strand":1,"end":140467240,"alleles":["C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs551035890"},{"seq_region_name":"7","id":"rs1794800175","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467244,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140467244},{"start":140467257,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140467257,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794800222","clinical_significance":[]},{"alleles":["C","T"],"end":140467260,"strand":1,"feature_type":"variation","start":140467260,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585482872","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794800336","clinical_significance":[],"alleles":["C","T"],"end":140467262,"strand":1,"feature_type":"variation","start":140467262,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1794800395","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467262,"feature_type":"variation","strand":1,"end":140467263,"alleles":["CC","C"]},{"alleles":["C","G"],"end":140467263,"feature_type":"variation","strand":1,"source":"dbSNP","start":140467263,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs911858818"},{"seq_region_name":"7","id":"rs1794800513","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467264,"source":"dbSNP","strand":1,"feature_type":"variation","end":140467264,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs1794800564","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140467265,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467265,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140467266,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467266,"clinical_significance":[],"seq_region_name":"7","id":"rs28413623"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1020749693","end":140467272,"alleles":["C","A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140467272,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140467273,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140467273,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs183378662"},{"seq_region_name":"7","id":"rs1327593366","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467274,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140467274},{"clinical_significance":[],"id":"rs548610386","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467275,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140467275},{"id":"rs1794800978","seq_region_name":"7","clinical_significance":[],"start":140467275,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["CCCCC","CCCC"],"end":140467279,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140467285,"alleles":["CCCCCTCCCCC","CCCCCTCCCCCTCCCCC"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467275,"source":"dbSNP","seq_region_name":"7","id":"rs1204075059","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467277,"feature_type":"variation","strand":1,"end":140467277,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1292293529"},{"start":140467279,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140467279,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1231799530","clinical_significance":[]},{"clinical_significance":[],"id":"rs2130312819","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467280,"feature_type":"variation","strand":1,"alleles":["T","-"],"end":140467280},{"end":140467281,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140467281,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1794801226","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130312846","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467282,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140467282},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794801304","source":"dbSNP","start":140467285,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140467285,"alleles":["C","G","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794801414","alleles":["A","G"],"end":140467286,"feature_type":"variation","strand":1,"source":"dbSNP","start":140467286,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140467287,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140467287,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs1334635951","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1289497578","seq_region_name":"7","source":"dbSNP","start":140467288,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TTTCTTTT","TTT"],"end":140467295,"feature_type":"variation","strand":1},{"end":140467295,"alleles":["TTTT","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140467292,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1232305712"},{"clinical_significance":[],"seq_region_name":"7","id":"rs567019574","source":"dbSNP","start":140467296,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140467296,"alleles":["A","G"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467300,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140467300,"clinical_significance":[],"seq_region_name":"7","id":"rs1034931308"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1053274523","end":140467301,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140467301,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1317641167","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140467307,"alleles":["T","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467307,"source":"dbSNP"},{"end":140467308,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140467308,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs143134966","clinical_significance":[]},{"seq_region_name":"7","id":"rs546265425","clinical_significance":[],"end":140467310,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140467310,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467313,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TTT","T"],"end":140467315,"seq_region_name":"7","id":"rs1459660288","clinical_significance":[]},{"end":140467319,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140467319,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs950307450","clinical_significance":[]},{"clinical_significance":[],"id":"rs1794802496","seq_region_name":"7","end":140467322,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140467322,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140467323,"alleles":["C","A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140467323,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794802591"},{"seq_region_name":"7","id":"rs1159809892","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467326,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140467326},{"end":140467328,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140467328,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794802801","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467330,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140467330,"clinical_significance":[],"seq_region_name":"7","id":"rs962835302"},{"seq_region_name":"7","id":"rs2130313132","clinical_significance":[],"start":140467333,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140467333,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467334,"feature_type":"variation","strand":1,"end":140467334,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794802987"},{"feature_type":"variation","strand":1,"end":140467335,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467335,"clinical_significance":[],"seq_region_name":"7","id":"rs1420864676"},{"strand":1,"feature_type":"variation","end":140467336,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467336,"source":"dbSNP","seq_region_name":"7","id":"rs1794803172","clinical_significance":[]},{"end":140467340,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140467340,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794803258"},{"seq_region_name":"7","id":"rs2130313209","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467349,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140467349},{"feature_type":"variation","strand":1,"end":140467350,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467350,"clinical_significance":[],"seq_region_name":"7","id":"rs1794803344"},{"feature_type":"variation","strand":1,"end":140467352,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467352,"clinical_significance":[],"seq_region_name":"7","id":"rs972785954"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1464835367","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140467359,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467359},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467361,"source":"dbSNP","strand":1,"feature_type":"variation","end":140467361,"alleles":["C","G"],"seq_region_name":"7","id":"rs1794803631","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467363,"source":"dbSNP","strand":1,"feature_type":"variation","end":140467363,"alleles":["A","C"],"seq_region_name":"7","id":"rs1214707547","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794803815","clinical_significance":[],"alleles":["C","T"],"end":140467365,"strand":1,"feature_type":"variation","start":140467365,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs918776921","clinical_significance":[],"strand":1,"feature_type":"variation","end":140467366,"alleles":["CT","CTCT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467365,"source":"dbSNP"},{"start":140467368,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140467368,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794804013","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467369,"feature_type":"variation","strand":1,"end":140467369,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794804107"},{"id":"rs1794804186","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140467372,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467372,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140467374,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467374,"source":"dbSNP","seq_region_name":"7","id":"rs1794804293","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794804378","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140467377,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467377},{"seq_region_name":"7","id":"rs1794804460","clinical_significance":[],"start":140467381,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140467381,"strand":1,"feature_type":"variation"},{"start":140467383,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140467383,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1255067507","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794804618","clinical_significance":[],"start":140467385,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140467385,"strand":1,"feature_type":"variation"},{"alleles":["CCC","CC"],"end":140467389,"feature_type":"variation","strand":1,"source":"dbSNP","start":140467387,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1794804691","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1794804783","clinical_significance":[],"start":140467389,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140467389,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1045417603","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467391,"feature_type":"variation","strand":1,"end":140467391,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1794804972","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140467394,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467394,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1468293586","seq_region_name":"7","alleles":["G","A"],"end":140467396,"feature_type":"variation","strand":1,"source":"dbSNP","start":140467396,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","T"],"end":140467400,"feature_type":"variation","strand":1,"source":"dbSNP","start":140467400,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1269234686","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794805234","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140467402,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467402},{"end":140467409,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140467409,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1210987673"},{"alleles":["G","A"],"end":140467420,"feature_type":"variation","strand":1,"source":"dbSNP","start":140467420,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794805389"},{"end":140467423,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140467423,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585483084","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs368997689","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467424,"feature_type":"variation","strand":1,"end":140467424,"alleles":["C","T"]},{"feature_type":"variation","strand":1,"end":140467425,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467425,"clinical_significance":[],"seq_region_name":"7","id":"rs866021596"},{"id":"rs1794805734","seq_region_name":"7","clinical_significance":[],"start":140467431,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140467431,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"alleles":["A","G"],"end":140467433,"strand":1,"feature_type":"variation","start":140467433,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1190231911","clinical_significance":[]},{"seq_region_name":"7","id":"rs1408223901","clinical_significance":[],"end":140467434,"alleles":["T","C","G"],"strand":1,"feature_type":"variation","start":140467434,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs905496031","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140467435,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467435},{"seq_region_name":"7","id":"rs1001142613","clinical_significance":[],"start":140467436,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","G","T"],"end":140467436,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1794806267","clinical_significance":[],"strand":1,"feature_type":"variation","end":140467439,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467439,"source":"dbSNP"},{"alleles":["T","G"],"end":140467442,"strand":1,"feature_type":"variation","start":140467442,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794806353","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794806436","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140467444,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467444},{"seq_region_name":"7","id":"rs187090120","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C","T"],"end":140467450,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467450,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140467453,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467453,"source":"dbSNP","seq_region_name":"7","id":"rs942943329","clinical_significance":[]},{"seq_region_name":"7","id":"rs898247389","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467461,"source":"dbSNP","strand":1,"feature_type":"variation","end":140467461,"alleles":["A","T"]},{"feature_type":"variation","strand":1,"end":140467464,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467464,"clinical_significance":[],"id":"rs1343317600","seq_region_name":"7"},{"alleles":["C","T"],"end":140467466,"strand":1,"feature_type":"variation","start":140467466,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1158319099","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["CGAGGTTTAACCATGTTGGC","C"],"end":140467485,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467466,"clinical_significance":[],"seq_region_name":"7","id":"rs1794806995"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1363163760","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467467,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140467467},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794807178","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467469,"feature_type":"variation","strand":1,"end":140467469,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1461845253","source":"dbSNP","start":140467470,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C","T"],"end":140467470,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1794807369","seq_region_name":"7","feature_type":"variation","strand":1,"end":140467471,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467471},{"clinical_significance":[],"seq_region_name":"7","id":"rs10273061","feature_type":"variation","strand":1,"alleles":["T","A","C","G"],"end":140467479,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467479},{"seq_region_name":"7","id":"rs914856458","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467481,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TT","T"],"end":140467482},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794807726","alleles":["C","T"],"end":140467485,"feature_type":"variation","strand":1,"source":"dbSNP","start":140467485,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467492,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140467492,"clinical_significance":[],"seq_region_name":"7","id":"rs1025861460"},{"source":"dbSNP","start":140467499,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140467499,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1485110495","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467507,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140467507,"seq_region_name":"7","id":"rs1585483207","clinical_significance":[]},{"clinical_significance":[],"id":"rs868065632","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467508,"feature_type":"variation","strand":1,"end":140467508,"alleles":["C","T"]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140467511,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467511,"source":"dbSNP","seq_region_name":"7","id":"rs1585483222","clinical_significance":[]},{"alleles":["A","C"],"end":140467513,"feature_type":"variation","strand":1,"source":"dbSNP","start":140467513,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1794808054","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1008533928","clinical_significance":[],"alleles":["G","C"],"end":140467514,"strand":1,"feature_type":"variation","start":140467514,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140467517,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140467517,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1018179921"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1439856729","source":"dbSNP","start":140467518,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140467518,"alleles":["T","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs964732555","clinical_significance":[],"end":140467520,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140467520,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140467521,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467521,"clinical_significance":[],"id":"rs1293212819","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467523,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140467523,"clinical_significance":[],"seq_region_name":"7","id":"rs1281919647"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794808451","source":"dbSNP","start":140467524,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140467524,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs556870883","clinical_significance":[],"start":140467525,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140467525,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"start":140467527,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140467527,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs926063420","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794808606","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467531,"source":"dbSNP","strand":1,"feature_type":"variation","end":140467531,"alleles":["G","C"]},{"alleles":["C","T"],"end":140467533,"strand":1,"feature_type":"variation","start":140467533,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs957406091","clinical_significance":[]},{"source":"dbSNP","start":140467534,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140467534,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1794808746","seq_region_name":"7"},{"id":"rs1304878259","seq_region_name":"7","clinical_significance":[],"start":140467541,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140467541,"alleles":["A","G","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1383651760","seq_region_name":"7","feature_type":"variation","strand":1,"end":140467542,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467542},{"start":140467543,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G","T"],"end":140467543,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1329088641","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs988995591","alleles":["G","A"],"end":140467544,"feature_type":"variation","strand":1,"source":"dbSNP","start":140467544,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs913365196","seq_region_name":"7","source":"dbSNP","start":140467545,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140467545,"alleles":["C","G","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs950340324","clinical_significance":[],"start":140467546,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140467546,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140467548,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140467548,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794809201"},{"start":140467549,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140467549,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs191918076","clinical_significance":[]},{"seq_region_name":"7","id":"rs927531434","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467550,"source":"dbSNP","strand":1,"feature_type":"variation","end":140467550,"alleles":["A","G","T"]},{"seq_region_name":"7","id":"rs1390966716","clinical_significance":[],"start":140467556,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140467556,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["G","C","T"],"end":140467557,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467557,"clinical_significance":[],"seq_region_name":"7","id":"rs1172871680"},{"strand":1,"feature_type":"variation","alleles":["T","TT"],"end":140467558,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467558,"source":"dbSNP","seq_region_name":"7","id":"rs1585483354","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467561,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140467561,"seq_region_name":"7","id":"rs1794809491","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794809541","source":"dbSNP","start":140467565,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140467567,"alleles":["CAC","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs963011640","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467566,"feature_type":"variation","strand":1,"end":140467566,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs1794809629","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467566,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","-"],"end":140467566},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467568,"feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140467568,"clinical_significance":[],"seq_region_name":"7","id":"rs937047107"},{"seq_region_name":"7","id":"rs1794809739","clinical_significance":[],"alleles":["T","-"],"end":140467568,"strand":1,"feature_type":"variation","start":140467568,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1794809793","seq_region_name":"7","end":140467571,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140467571,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140467572,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140467572,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs1182940232","seq_region_name":"7","clinical_significance":[]},{"start":140467576,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140467576,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794809897","clinical_significance":[]},{"clinical_significance":[],"id":"rs1486908268","seq_region_name":"7","source":"dbSNP","start":140467578,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140467578,"alleles":["C","T"],"feature_type":"variation","strand":1},{"start":140467579,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140467579,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1037992439","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130314932","source":"dbSNP","start":140467581,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140467581,"alleles":["T","C"],"feature_type":"variation","strand":1},{"id":"rs2130314957","seq_region_name":"7","clinical_significance":[],"start":140467590,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140467590,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140467593,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140467593,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1208045252"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467594,"feature_type":"variation","strand":1,"alleles":["CC","CCC"],"end":140467595,"clinical_significance":[],"seq_region_name":"7","id":"rs1794810094"},{"seq_region_name":"7","id":"rs1794810150","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467595,"source":"dbSNP","strand":1,"feature_type":"variation","end":140467607,"alleles":["CATCTGCATCTGC","CATCTGC"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs898254027","source":"dbSNP","start":140467598,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140467598,"alleles":["C","G","T"],"feature_type":"variation","strand":1},{"end":140467603,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","start":140467603,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs993855116","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1046906304","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140467604,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467604},{"clinical_significance":[],"seq_region_name":"7","id":"rs890983856","feature_type":"variation","strand":1,"end":140467605,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467605},{"clinical_significance":[],"seq_region_name":"7","id":"rs1305546642","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467613,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140467613},{"clinical_significance":[],"seq_region_name":"7","id":"rs1174989511","end":140467614,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140467614,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs987006941","clinical_significance":[],"strand":1,"feature_type":"variation","end":140467615,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467615,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794810570","source":"dbSNP","start":140467615,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","TT"],"end":140467615,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1357247011","clinical_significance":[],"end":140467619,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140467619,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs182896855","clinical_significance":[],"strand":1,"feature_type":"variation","end":140467624,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467624,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1794810731","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467626,"source":"dbSNP","strand":1,"feature_type":"variation","end":140467626,"alleles":["C","A","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467628,"feature_type":"variation","strand":1,"alleles":["AAAA","AAA"],"end":140467631,"clinical_significance":[],"seq_region_name":"7","id":"rs1190031324"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140467630,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467630,"clinical_significance":[],"id":"rs1794810846","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140467633,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467633,"source":"dbSNP","id":"rs1794810900","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563093206","feature_type":"variation","strand":1,"end":140467634,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467634},{"seq_region_name":"7","id":"rs554592291","clinical_significance":[],"alleles":["G","A","T"],"end":140467635,"strand":1,"feature_type":"variation","start":140467635,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794811068","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467636,"feature_type":"variation","strand":1,"end":140467639,"alleles":["GAAC","-"]},{"seq_region_name":"7","id":"rs964333830","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467643,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140467643},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140467644,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467644,"source":"dbSNP","id":"rs1018649584","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1460713605","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140467646,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467646,"source":"dbSNP"},{"source":"dbSNP","start":140467647,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140467647,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1372737968","seq_region_name":"7"},{"end":140467652,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140467652,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1460783249","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140467653,"alleles":["T","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467653,"clinical_significance":[],"id":"rs914928581","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140467655,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467655,"clinical_significance":[],"seq_region_name":"7","id":"rs1794811462"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467657,"feature_type":"variation","strand":1,"end":140467657,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1170876881"},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140467659,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467659,"clinical_significance":[],"seq_region_name":"7","id":"rs573053579"},{"seq_region_name":"7","id":"rs963951287","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140467662,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467662,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1794811679","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467665,"source":"dbSNP","strand":1,"feature_type":"variation","end":140467665,"alleles":["C","T"]},{"source":"dbSNP","start":140467669,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140467669,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794811734"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1187924935","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467670,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140467670},{"seq_region_name":"7","id":"rs1794811851","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467671,"source":"dbSNP","strand":1,"feature_type":"variation","end":140467671,"alleles":["G","A"]},{"end":140467672,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140467672,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1485040498"},{"clinical_significance":[],"id":"rs996188843","seq_region_name":"7","alleles":["C","T"],"end":140467675,"feature_type":"variation","strand":1,"source":"dbSNP","start":140467675,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs540468220","end":140467676,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140467676,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140467683,"alleles":["GCAAAG","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467678,"clinical_significance":[],"id":"rs1794812098","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1794812160","clinical_significance":[],"start":140467683,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140467683,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1032970877","clinical_significance":[],"start":140467687,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","G","T"],"end":140467687,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1794812294","seq_region_name":"7","source":"dbSNP","start":140467689,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140467689,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140467696,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467696,"clinical_significance":[],"seq_region_name":"7","id":"rs138277443"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1415441876","alleles":["T","C"],"end":140467701,"feature_type":"variation","strand":1,"source":"dbSNP","start":140467701,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1794812473","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467704,"source":"dbSNP","strand":1,"feature_type":"variation","end":140467704,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1214039522","clinical_significance":[],"start":140467706,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140467706,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140467708,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467708,"source":"dbSNP","seq_region_name":"7","id":"rs989271989","clinical_significance":[]},{"start":140467709,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["ACACA","ACA"],"end":140467713,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794812630","clinical_significance":[]},{"id":"rs1295704908","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140467710,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467710,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs4424177","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467711,"feature_type":"variation","strand":1,"end":140467711,"alleles":["A","G"]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140467712,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467712,"clinical_significance":[],"seq_region_name":"7","id":"rs1794812843"},{"clinical_significance":[],"seq_region_name":"7","id":"rs939066777","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467714,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140467714},{"source":"dbSNP","start":140467721,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["GG","G"],"end":140467722,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794812894"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1228176224","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467725,"feature_type":"variation","strand":1,"end":140467729,"alleles":["GGGGG","GGG","GGGGGG"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794813007","end":140467728,"alleles":["G","C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140467728,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467729,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140467729,"clinical_significance":[],"seq_region_name":"7","id":"rs1794813155"},{"feature_type":"variation","strand":1,"end":140467730,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467730,"clinical_significance":[],"id":"rs1794813214","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467734,"source":"dbSNP","strand":1,"feature_type":"variation","end":140467734,"alleles":["G","C"],"seq_region_name":"7","id":"rs1794813273","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140467740,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467740,"clinical_significance":[],"id":"rs1336417536","seq_region_name":"7"},{"clinical_significance":[],"id":"rs971994866","seq_region_name":"7","feature_type":"variation","strand":1,"end":140467741,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467741},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794813443","feature_type":"variation","strand":1,"end":140467742,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467742},{"end":140467745,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140467745,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794813493"},{"seq_region_name":"7","id":"rs1794813543","clinical_significance":[],"alleles":["T","C"],"end":140467749,"strand":1,"feature_type":"variation","start":140467749,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467754,"source":"dbSNP","strand":1,"feature_type":"variation","end":140467754,"alleles":["G","T"],"seq_region_name":"7","id":"rs1389752779","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1274084774","alleles":["C","A","T"],"end":140467759,"feature_type":"variation","strand":1,"source":"dbSNP","start":140467759,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1308918900","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467761,"feature_type":"variation","strand":1,"alleles":["GGG","GGGG"],"end":140467763},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467762,"feature_type":"variation","strand":1,"end":140467762,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1463319651"},{"feature_type":"variation","strand":1,"end":140467768,"alleles":["T","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467768,"clinical_significance":[],"id":"rs1201957997","seq_region_name":"7"},{"end":140467769,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140467769,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1794813904","seq_region_name":"7","clinical_significance":[]},{"end":140467772,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140467772,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1794813960","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1273427870","clinical_significance":[],"end":140467773,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140467773,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140467774,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140467774,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs981630232"},{"alleles":["GGG","GGGGGG"],"end":140467776,"strand":1,"feature_type":"variation","start":140467774,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585483663","clinical_significance":[]},{"seq_region_name":"7","id":"rs1473237383","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140467775,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467775,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1189435467","seq_region_name":"7","source":"dbSNP","start":140467776,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140467776,"alleles":["G","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs927583642","clinical_significance":[],"start":140467777,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","G","T"],"end":140467777,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs937556001","source":"dbSNP","start":140467778,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140467778,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585483690","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140467780,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467780},{"end":140467781,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140467781,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1585483693","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1249354727","feature_type":"variation","strand":1,"end":140467784,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467784},{"clinical_significance":[],"seq_region_name":"7","id":"rs953324945","alleles":["T","C"],"end":140467786,"feature_type":"variation","strand":1,"source":"dbSNP","start":140467786,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140467789,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467789,"clinical_significance":[],"seq_region_name":"7","id":"rs2130316410"},{"seq_region_name":"7","id":"rs1794814661","clinical_significance":[],"end":140467791,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140467791,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs894944740","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467792,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140467792},{"clinical_significance":[],"seq_region_name":"7","id":"rs1186899723","feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140467795,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467795},{"source":"dbSNP","start":140467798,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A","C","G"],"end":140467798,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1012185714"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467799,"feature_type":"variation","strand":1,"end":140467802,"alleles":["TCAA","-"],"clinical_significance":[],"id":"rs1794814928","seq_region_name":"7"},{"alleles":["C","A","T"],"end":140467800,"feature_type":"variation","strand":1,"source":"dbSNP","start":140467800,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs187750299"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467808,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140467808,"seq_region_name":"7","id":"rs1794815061","clinical_significance":[]},{"id":"rs1794815115","seq_region_name":"7","clinical_significance":[],"start":140467809,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140467809,"strand":1,"feature_type":"variation"},{"id":"rs1563093283","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467813,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140467813},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467819,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140467819,"clinical_significance":[],"seq_region_name":"7","id":"rs1794815234"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467820,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140467820,"clinical_significance":[],"seq_region_name":"7","id":"rs919565767"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467821,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140467821,"id":"rs929645727","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794815430","feature_type":"variation","strand":1,"alleles":["-","C"],"end":140467823,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467824},{"source":"dbSNP","start":140467824,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140467824,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1794815484","seq_region_name":"7"},{"start":140467825,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140467827,"alleles":["AAA","AAAA"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1236907507","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs979379081","source":"dbSNP","start":140467827,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140467827,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1794815644","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140467828,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467828,"source":"dbSNP"},{"end":140467829,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140467829,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1794815706","seq_region_name":"7"},{"end":140467831,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140467831,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs867356813"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794815830","source":"dbSNP","start":140467832,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140467831,"alleles":["-","CATT"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs890878961","clinical_significance":[],"strand":1,"feature_type":"variation","end":140467832,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467832,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs943905737","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467833,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140467833},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794816022","feature_type":"variation","strand":1,"alleles":["CC","C"],"end":140467834,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467833},{"id":"rs1794816078","seq_region_name":"7","clinical_significance":[],"end":140467833,"alleles":["-","A"],"strand":1,"feature_type":"variation","start":140467834,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1369220367","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140467834,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467834},{"clinical_significance":[],"seq_region_name":"7","id":"rs796785261","feature_type":"variation","strand":1,"end":140467841,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467841},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130316870","alleles":["T","A"],"end":140467846,"feature_type":"variation","strand":1,"source":"dbSNP","start":140467846,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs2130316883","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140467850,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467850,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467852,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140467852,"clinical_significance":[],"seq_region_name":"7","id":"rs1401655064"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794816341","end":140467853,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140467853,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794816404","source":"dbSNP","start":140467854,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140467854,"alleles":["T","C"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467858,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140467858,"clinical_significance":[],"seq_region_name":"7","id":"rs1585483828"},{"clinical_significance":[],"id":"rs1387715287","seq_region_name":"7","feature_type":"variation","strand":1,"end":140467862,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467862},{"seq_region_name":"7","id":"rs1794816547","clinical_significance":[],"start":140467865,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140467865,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467867,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140467867,"clinical_significance":[],"id":"rs1447883365","seq_region_name":"7"},{"end":140467869,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140467869,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs531589624","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","T"],"end":140467872,"strand":1,"feature_type":"variation","start":140467872,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794816724","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1450957529","source":"dbSNP","start":140467876,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140467876,"alleles":["C","G","T"],"feature_type":"variation","strand":1},{"start":140467884,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140467884,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1008280893","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467885,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140467885,"clinical_significance":[],"seq_region_name":"7","id":"rs1173866757"},{"seq_region_name":"7","id":"rs1794816947","clinical_significance":[],"start":140467889,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140467889,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1794816996","clinical_significance":[],"start":140467890,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140467890,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794817049","source":"dbSNP","start":140467891,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C","G"],"end":140467891,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1794817115","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467892,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140467892},{"clinical_significance":[],"seq_region_name":"7","id":"rs1455264258","alleles":["T","C"],"end":140467893,"feature_type":"variation","strand":1,"source":"dbSNP","start":140467893,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["T","C"],"end":140467894,"feature_type":"variation","strand":1,"source":"dbSNP","start":140467894,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794817214"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1000757767","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467895,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140467895},{"feature_type":"variation","strand":1,"end":140467897,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467897,"clinical_significance":[],"seq_region_name":"7","id":"rs1794817321"},{"clinical_significance":[],"id":"rs1794817370","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467899,"feature_type":"variation","strand":1,"end":140467899,"alleles":["G","A"]},{"alleles":["G","A"],"end":140467903,"feature_type":"variation","strand":1,"source":"dbSNP","start":140467903,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1033023059"},{"clinical_significance":[],"id":"rs753873956","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467905,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140467905},{"seq_region_name":"7","id":"rs1794817557","clinical_significance":[],"start":140467906,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140467906,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467907,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140467907,"clinical_significance":[],"seq_region_name":"7","id":"rs530055616"},{"start":140467909,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140467909,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1020827055","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794817743","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467914,"source":"dbSNP","strand":1,"feature_type":"variation","end":140467914,"alleles":["A","G"]},{"end":140467918,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140467918,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794817814","clinical_significance":[]},{"end":140467919,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140467919,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs964535173"},{"seq_region_name":"7","id":"rs1794817927","clinical_significance":[],"start":140467923,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140467923,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs192670837","alleles":["C","A","T"],"end":140467926,"feature_type":"variation","strand":1,"source":"dbSNP","start":140467926,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs982024869","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467927,"feature_type":"variation","strand":1,"end":140467927,"alleles":["G","A"]},{"end":140467932,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140467932,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794818429","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585483953","clinical_significance":[],"end":140467933,"alleles":["T","C","G"],"strand":1,"feature_type":"variation","start":140467933,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140467934,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140467934,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794818556","clinical_significance":[]},{"id":"rs1794818601","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467935,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140467935},{"seq_region_name":"7","id":"rs1794818656","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467938,"source":"dbSNP","strand":1,"feature_type":"variation","end":140467938,"alleles":["G","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585483960","end":140467939,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140467939,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1794818760","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467941,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140467941},{"source":"dbSNP","start":140467942,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140467942,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1350035745"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467943,"source":"dbSNP","strand":1,"feature_type":"variation","end":140467943,"alleles":["G","A"],"seq_region_name":"7","id":"rs1281200975","clinical_significance":[]},{"seq_region_name":"7","id":"rs184293482","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140467950,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467950,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140467951,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467951,"source":"dbSNP","id":"rs1296494628","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140467953,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467953,"clinical_significance":[],"id":"rs1794819041","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140467957,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467957,"clinical_significance":[],"seq_region_name":"7","id":"rs1345909894"},{"clinical_significance":[],"id":"rs958960404","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140467958,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467958},{"clinical_significance":[],"id":"rs974326031","seq_region_name":"7","alleles":["T","C"],"end":140467963,"feature_type":"variation","strand":1,"source":"dbSNP","start":140467963,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["TT","T"],"end":140467964,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467963,"source":"dbSNP","seq_region_name":"7","id":"rs1794819265","clinical_significance":[]},{"start":140467964,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140467964,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794819318","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467965,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140467965,"seq_region_name":"7","id":"rs1794819371","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794819421","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467965,"feature_type":"variation","strand":1,"alleles":["G","-"],"end":140467965},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585484021","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467967,"feature_type":"variation","strand":1,"end":140467967,"alleles":["A","C"]},{"seq_region_name":"7","id":"rs1585484034","clinical_significance":[],"end":140467969,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","start":140467969,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1348152894","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140467971,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467971},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467973,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140467973,"seq_region_name":"7","id":"rs920160166","clinical_significance":[]},{"clinical_significance":[],"id":"rs2130317796","seq_region_name":"7","alleles":["T","C"],"end":140467976,"feature_type":"variation","strand":1,"source":"dbSNP","start":140467976,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140467977,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140467977,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1022321620"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467980,"source":"dbSNP","strand":1,"feature_type":"variation","end":140467980,"alleles":["C","A","T"],"seq_region_name":"7","id":"rs1277493987","clinical_significance":[]},{"seq_region_name":"7","id":"rs1376611567","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467981,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AA","A"],"end":140467982},{"seq_region_name":"7","id":"rs1794819915","clinical_significance":[],"end":140467982,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140467982,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1794819966","clinical_significance":[],"strand":1,"feature_type":"variation","end":140467985,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467985,"source":"dbSNP"},{"source":"dbSNP","start":140467986,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140467986,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs929672180"},{"feature_type":"variation","strand":1,"end":140467988,"alleles":["G","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467988,"clinical_significance":[],"seq_region_name":"7","id":"rs1216354633"},{"seq_region_name":"7","id":"rs982462604","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140467989,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140467989,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467990,"feature_type":"variation","strand":1,"end":140467990,"alleles":["G","A"],"clinical_significance":[],"id":"rs751283056","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140467998,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140467998,"clinical_significance":[],"seq_region_name":"7","id":"rs1794820281"},{"seq_region_name":"7","id":"rs1794820345","clinical_significance":[],"start":140467999,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TCTC","TCTCTC"],"end":140468002,"strand":1,"feature_type":"variation"},{"end":140468000,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140468000,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1309611011"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1373948050","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468001,"feature_type":"variation","strand":1,"end":140468001,"alleles":["T","A"]},{"source":"dbSNP","start":140468001,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140468001,"alleles":["T","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130318004"},{"feature_type":"variation","strand":1,"end":140468001,"alleles":["-","A","AA","AAAA","AAAAA","AAAAAA","AAAAAAA","AAAAAAAA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468002,"clinical_significance":[],"seq_region_name":"7","id":"rs1794820504"},{"seq_region_name":"7","id":"rs1395642788","clinical_significance":[],"end":140468002,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140468002,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["C","CC"],"end":140468002,"feature_type":"variation","strand":1,"source":"dbSNP","start":140468002,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1446293979"},{"source":"dbSNP","start":140468002,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","-"],"end":140468002,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794820753"},{"end":140468002,"alleles":["-","TCAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140468003,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1213061941"},{"feature_type":"variation","strand":1,"end":140468003,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468003,"clinical_significance":[],"seq_region_name":"7","id":"rs1190031276"},{"clinical_significance":[],"seq_region_name":"7","id":"rs566154288","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468003,"feature_type":"variation","strand":1,"alleles":["AAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAA","AAAAAAAAAAAAAA","AAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAA"],"end":140468021},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794820921","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468006,"feature_type":"variation","strand":1,"end":140468006,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794820972","source":"dbSNP","start":140468008,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140468007,"alleles":["-","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs977732321","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468008,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140468008},{"clinical_significance":[],"id":"rs943765823","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","C","T"],"end":140468011,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468011},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468012,"feature_type":"variation","strand":1,"end":140468014,"alleles":["AAA","AAATAAA"],"clinical_significance":[],"seq_region_name":"7","id":"rs1256976543"},{"feature_type":"variation","strand":1,"alleles":["AAAAAAAA","AAAAAAAACAAAAAAAA"],"end":140468019,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468012,"clinical_significance":[],"seq_region_name":"7","id":"rs1794821224"},{"seq_region_name":"7","id":"rs1794821270","clinical_significance":[],"end":140468014,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140468014,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140468015,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["-","T"],"end":140468014,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1187682365","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs923576423","end":140468015,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140468015,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1794821407","clinical_significance":[],"end":140468015,"alleles":["-","TAAAT"],"strand":1,"feature_type":"variation","start":140468016,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140468016,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140468017,"alleles":["AA","AATAA"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1563093396","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794821497","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468016,"feature_type":"variation","strand":1,"end":140468018,"alleles":["AAA","AAATAAA"]},{"start":140468016,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AAAAA","AAAAATAAAAA"],"end":140468020,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1563093399","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1439711408","source":"dbSNP","start":140468020,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140468020,"alleles":["A","ATA"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1271191207","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468022,"feature_type":"variation","strand":1,"alleles":["T","TT"],"end":140468022},{"start":140468022,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140468022,"alleles":["T","A","C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1313596720","clinical_significance":[]},{"id":"rs1794821813","seq_region_name":"7","clinical_significance":[],"start":140468022,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140468022,"alleles":["T","-"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1175628533","feature_type":"variation","strand":1,"end":140468023,"alleles":["G","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468023},{"clinical_significance":[],"seq_region_name":"7","id":"rs527861804","feature_type":"variation","strand":1,"end":140468024,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468024},{"start":140468025,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140468025,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs899636206","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","AAAAAAAA"],"end":140468025,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468025,"source":"dbSNP","id":"rs1794822092","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs992295737","clinical_significance":[],"alleles":["G","T"],"end":140468028,"strand":1,"feature_type":"variation","start":140468028,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1794822219","clinical_significance":[],"start":140468030,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140468030,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1413948523","seq_region_name":"7","feature_type":"variation","strand":1,"end":140468032,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468032},{"clinical_significance":[],"id":"rs936474454","seq_region_name":"7","source":"dbSNP","start":140468033,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140468033,"alleles":["A","G"],"feature_type":"variation","strand":1},{"id":"rs1283028524","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468034,"source":"dbSNP","strand":1,"feature_type":"variation","end":140468034,"alleles":["G","A"]},{"feature_type":"variation","strand":1,"end":140468035,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468035,"clinical_significance":[],"id":"rs1794822433","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1794822485","clinical_significance":[],"strand":1,"feature_type":"variation","end":140468038,"alleles":["CACA","CA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468035,"source":"dbSNP"},{"alleles":["C","G"],"end":140468037,"feature_type":"variation","strand":1,"source":"dbSNP","start":140468037,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585484270"},{"id":"rs1585484274","seq_region_name":"7","clinical_significance":[],"start":140468039,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140468039,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585484278","end":140468040,"alleles":["A","C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140468040,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468044,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140468044,"clinical_significance":[],"seq_region_name":"7","id":"rs1585484284"},{"seq_region_name":"7","id":"rs916315424","clinical_significance":[],"strand":1,"feature_type":"variation","end":140468049,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468049,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468050,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140468050,"seq_region_name":"7","id":"rs1794822858","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140468056,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468056,"source":"dbSNP","seq_region_name":"7","id":"rs1794822908","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140468057,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468057,"clinical_significance":[],"seq_region_name":"7","id":"rs1053724521"},{"seq_region_name":"7","id":"rs1319611897","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468057,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TTCATTTT","TTCATTTTCATTTT"],"end":140468064},{"seq_region_name":"7","id":"rs1794823102","clinical_significance":[],"alleles":["T","C"],"end":140468058,"strand":1,"feature_type":"variation","start":140468058,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["A","G"],"end":140468060,"feature_type":"variation","strand":1,"source":"dbSNP","start":140468060,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585484309"},{"seq_region_name":"7","id":"rs1794823208","clinical_significance":[],"strand":1,"feature_type":"variation","end":140468061,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468061,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140468067,"alleles":["TTTTTTT","TTTTTT","TTTTTTTT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468061,"clinical_significance":[],"seq_region_name":"7","id":"rs1038198468"},{"start":140468062,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140468062,"alleles":["T","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1320234205","clinical_significance":[]},{"alleles":["T","G"],"end":140468063,"feature_type":"variation","strand":1,"source":"dbSNP","start":140468063,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1459758735","seq_region_name":"7"},{"seq_region_name":"7","id":"rs892379903","clinical_significance":[],"start":140468065,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140468065,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1371300647","clinical_significance":[],"strand":1,"feature_type":"variation","end":140468068,"alleles":["C","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468068,"source":"dbSNP"},{"seq_region_name":"7","id":"rs929839428","clinical_significance":[],"alleles":["A","AA"],"end":140468069,"strand":1,"feature_type":"variation","start":140468069,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140468071,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140468071,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1300660353","clinical_significance":[]},{"start":140468075,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TCCATCTACACAGTCCAT","TCCAT"],"end":140468092,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1471215154","clinical_significance":[]},{"end":140468076,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140468076,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1794823676","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1231377770","clinical_significance":[],"start":140468078,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140468078,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs2130319038","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140468081,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468081},{"clinical_significance":[],"id":"rs2130319052","seq_region_name":"7","end":140468083,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140468083,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1010686058","feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140468085,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468085},{"seq_region_name":"7","id":"rs1794823839","clinical_significance":[],"strand":1,"feature_type":"variation","end":140468088,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468088,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1275501901","source":"dbSNP","start":140468089,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140468089,"alleles":["C","A","T"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140468091,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468091,"clinical_significance":[],"seq_region_name":"7","id":"rs1047100679"},{"feature_type":"variation","strand":1,"end":140468096,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468096,"clinical_significance":[],"seq_region_name":"7","id":"rs1020250215"},{"clinical_significance":[],"id":"rs1334694553","seq_region_name":"7","source":"dbSNP","start":140468097,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140468097,"feature_type":"variation","strand":1},{"alleles":["G","C"],"end":140468099,"strand":1,"feature_type":"variation","start":140468099,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794824117","clinical_significance":[]},{"seq_region_name":"7","id":"rs907299882","clinical_significance":[],"start":140468104,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140468104,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"id":"rs1794824329","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468104,"source":"dbSNP","strand":1,"feature_type":"variation","end":140468111,"alleles":["CTTCTTCT","CTTCT"]},{"end":140468110,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140468110,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1223806618","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140468111,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468111,"source":"dbSNP","seq_region_name":"7","id":"rs1585484404","clinical_significance":[]},{"seq_region_name":"7","id":"rs891102539","clinical_significance":[],"start":140468115,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140468115,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468116,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140468116,"clinical_significance":[],"seq_region_name":"7","id":"rs1794824568"},{"seq_region_name":"7","id":"rs1008333028","clinical_significance":[],"alleles":["A","G"],"end":140468125,"strand":1,"feature_type":"variation","start":140468125,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1794824624","clinical_significance":[],"start":140468126,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140468126,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140468139,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140468139,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1794824691","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1018795862","clinical_significance":[],"start":140468140,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140468140,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"start":140468141,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140468141,"alleles":["A","G","T"],"strand":1,"feature_type":"variation","id":"rs1794824816","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140468144,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468144,"clinical_significance":[],"seq_region_name":"7","id":"rs899899640"},{"seq_region_name":"7","id":"rs1665830736","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468153,"source":"dbSNP","strand":1,"feature_type":"variation","end":140468153,"alleles":["C","G"]},{"end":140468155,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140468155,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs756798463","clinical_significance":[]},{"clinical_significance":[],"id":"rs1012199841","seq_region_name":"7","source":"dbSNP","start":140468157,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140468157,"feature_type":"variation","strand":1},{"end":140468162,"alleles":["CACA","CA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140468159,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1021758760"},{"start":140468165,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","T"],"end":140468165,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585484447","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140468166,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468166,"clinical_significance":[],"seq_region_name":"7","id":"rs967613125"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794825232","alleles":["A","C"],"end":140468167,"feature_type":"variation","strand":1,"source":"dbSNP","start":140468167,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140468168,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TT","TTT"],"end":140468169,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1402487962","clinical_significance":[]},{"id":"rs1794825332","seq_region_name":"7","clinical_significance":[],"start":140468169,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140468169,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1405963451","clinical_significance":[],"strand":1,"feature_type":"variation","end":140468178,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468178,"source":"dbSNP"},{"clinical_significance":[],"id":"rs977616038","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468180,"feature_type":"variation","strand":1,"alleles":["TG","TGTG"],"end":140468181},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468183,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140468183,"clinical_significance":[],"seq_region_name":"7","id":"rs1454827705"},{"seq_region_name":"7","id":"rs1255128364","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468184,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140468184},{"end":140468186,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140468186,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs925149171","clinical_significance":[]},{"end":140468187,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140468187,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1002930410","clinical_significance":[]},{"start":140468191,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140468191,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1030643352","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140468192,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468192,"source":"dbSNP","id":"rs1243177310","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1034384783","end":140468193,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140468193,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468203,"feature_type":"variation","strand":1,"alleles":["CTCTC","CTC"],"end":140468207,"clinical_significance":[],"seq_region_name":"7","id":"rs1794825837"},{"start":140468208,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G","T"],"end":140468208,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130319597","clinical_significance":[]},{"end":140468212,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140468212,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1218646111"},{"clinical_significance":[],"seq_region_name":"7","id":"rs552392475","feature_type":"variation","strand":1,"end":140468219,"alleles":["A","C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468219},{"clinical_significance":[],"seq_region_name":"7","id":"rs974211405","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140468227,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468227},{"id":"rs1027229948","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140468230,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468230,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794826125","alleles":["C","G"],"end":140468231,"feature_type":"variation","strand":1,"source":"dbSNP","start":140468231,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1348109613","seq_region_name":"7","alleles":["A","G","T"],"end":140468233,"feature_type":"variation","strand":1,"source":"dbSNP","start":140468233,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1305209635","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468234,"feature_type":"variation","strand":1,"end":140468234,"alleles":["G","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794826300","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468236,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140468236},{"clinical_significance":[],"seq_region_name":"7","id":"rs1438419065","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468236,"feature_type":"variation","strand":1,"alleles":["CACA","CA"],"end":140468239},{"end":140468241,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140468241,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794826402","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs189578801","source":"dbSNP","start":140468244,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140468244,"feature_type":"variation","strand":1},{"id":"rs1794826498","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468246,"source":"dbSNP","strand":1,"feature_type":"variation","end":140468246,"alleles":["A","G"]},{"id":"rs1289368227","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140468248,"strand":1,"feature_type":"variation","start":140468248,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs916350334","source":"dbSNP","start":140468251,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140468251,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1469099751","clinical_significance":[],"end":140468257,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140468257,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["T","C"],"end":140468263,"strand":1,"feature_type":"variation","start":140468263,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs947826724","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140468266,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468266,"clinical_significance":[],"seq_region_name":"7","id":"rs982860581"},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140468269,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468269,"clinical_significance":[],"seq_region_name":"7","id":"rs1435448940"},{"seq_region_name":"7","id":"rs1195778611","clinical_significance":[],"alleles":["A","G"],"end":140468271,"strand":1,"feature_type":"variation","start":140468271,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794826911","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140468272,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468272},{"feature_type":"variation","strand":1,"end":140468277,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468277,"clinical_significance":[],"seq_region_name":"7","id":"rs1794826972"},{"clinical_significance":[],"id":"rs1172060267","seq_region_name":"7","end":140468278,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140468278,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140468280,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468280,"clinical_significance":[],"seq_region_name":"7","id":"rs974315723"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1188676384","end":140468286,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140468286,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1794827223","seq_region_name":"7","end":140468288,"alleles":["T","TT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140468288,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1794827273","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468289,"source":"dbSNP","strand":1,"feature_type":"variation","end":140468289,"alleles":["C","A"]},{"feature_type":"variation","strand":1,"end":140468293,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468293,"clinical_significance":[],"seq_region_name":"7","id":"rs1477773997"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468294,"feature_type":"variation","strand":1,"end":140468294,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794827370"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468295,"source":"dbSNP","strand":1,"feature_type":"variation","end":140468295,"alleles":["C","A","T"],"id":"rs1485141627","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468299,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140468299,"seq_region_name":"7","id":"rs1794827478","clinical_significance":[]},{"start":140468302,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140468302,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130320112","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468303,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140468303,"id":"rs1794827520","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs538308304","alleles":["C","G"],"end":140468305,"feature_type":"variation","strand":1,"source":"dbSNP","start":140468305,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["A","G"],"end":140468307,"feature_type":"variation","strand":1,"source":"dbSNP","start":140468307,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1215203187","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468308,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140468308,"id":"rs1485743092","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794827668","feature_type":"variation","strand":1,"end":140468309,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468309},{"clinical_significance":[],"seq_region_name":"7","id":"rs929890232","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468310,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140468310},{"alleles":["C","A"],"end":140468311,"feature_type":"variation","strand":1,"source":"dbSNP","start":140468311,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs765005610"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794827854","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140468312,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468312},{"seq_region_name":"7","id":"rs1585484666","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468313,"source":"dbSNP","strand":1,"feature_type":"variation","end":140468313,"alleles":["G","A"]},{"end":140468315,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140468315,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs868347647","clinical_significance":[]},{"end":140468318,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140468318,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1410812485"},{"seq_region_name":"7","id":"rs1456061362","clinical_significance":[],"start":140468320,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140468320,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs192420257","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468329,"feature_type":"variation","strand":1,"end":140468329,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1794828204","clinical_significance":[],"start":140468330,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140468330,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140468332,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140468332,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1046989320","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1359727080","feature_type":"variation","strand":1,"end":140468336,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468336},{"clinical_significance":[],"seq_region_name":"7","id":"rs1395618720","source":"dbSNP","start":140468337,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140468337,"alleles":["T","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1415451324","alleles":["T","A","G"],"end":140468338,"feature_type":"variation","strand":1,"source":"dbSNP","start":140468338,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140468339,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140468339,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs61455390","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140468340,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468340,"clinical_significance":[],"seq_region_name":"7","id":"rs535899968"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1465681550","source":"dbSNP","start":140468346,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140468346,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140468348,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140468348,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1366565110"},{"id":"rs1039698726","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468349,"source":"dbSNP","strand":1,"feature_type":"variation","end":140468349,"alleles":["C","A","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1172939445","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140468352,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468352},{"clinical_significance":[],"id":"rs1794828911","seq_region_name":"7","source":"dbSNP","start":140468353,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140468353,"alleles":["T","G"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140468355,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468355,"clinical_significance":[],"seq_region_name":"7","id":"rs2130320575"},{"clinical_significance":[],"id":"rs1330134315","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468357,"feature_type":"variation","strand":1,"end":140468357,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs10216203","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140468358,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468358,"source":"dbSNP"},{"end":140468359,"alleles":["TG","CA"],"strand":1,"feature_type":"variation","start":140468358,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs386718464","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs573216217","source":"dbSNP","start":140468359,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140468359,"alleles":["G","A","C"],"feature_type":"variation","strand":1},{"alleles":["G","A"],"end":140468364,"strand":1,"feature_type":"variation","start":140468364,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1011629696","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1348470656","alleles":["C","T"],"end":140468367,"feature_type":"variation","strand":1,"source":"dbSNP","start":140468367,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130320705","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140468369,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468369},{"alleles":["T","C"],"end":140468371,"feature_type":"variation","strand":1,"source":"dbSNP","start":140468371,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1043631715"},{"seq_region_name":"7","id":"rs903339796","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140468375,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468375,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140468376,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468376,"clinical_significance":[],"id":"rs1794829516","seq_region_name":"7"},{"start":140468377,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","TT"],"end":140468377,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794829578","clinical_significance":[]},{"end":140468379,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140468379,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs184731575","clinical_significance":[]},{"start":140468380,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140468380,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794829700","clinical_significance":[]},{"seq_region_name":"7","id":"rs998961348","clinical_significance":[],"end":140468381,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140468381,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140468382,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140468382,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs188704676","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468383,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140468383,"clinical_significance":[],"seq_region_name":"7","id":"rs1273705408"},{"seq_region_name":"7","id":"rs960272870","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140468387,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468387,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794830028","alleles":["T","C"],"end":140468389,"feature_type":"variation","strand":1,"source":"dbSNP","start":140468389,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140468391,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140468391,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794830077"},{"alleles":["C","A","G"],"end":140468394,"strand":1,"feature_type":"variation","start":140468394,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1013709057","clinical_significance":[]},{"seq_region_name":"7","id":"rs907230068","clinical_significance":[],"start":140468404,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140468404,"alleles":["C","A","T"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468406,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140468406,"id":"rs547851621","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","C"],"end":140468410,"feature_type":"variation","strand":1,"source":"dbSNP","start":140468410,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1395559811","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1794830344","clinical_significance":[],"start":140468412,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140468412,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs2130321037","seq_region_name":"7","alleles":["G","A"],"end":140468417,"feature_type":"variation","strand":1,"source":"dbSNP","start":140468417,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1374270931","alleles":["G","A","C"],"end":140468419,"feature_type":"variation","strand":1,"source":"dbSNP","start":140468419,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468423,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140468423,"seq_region_name":"7","id":"rs1300168913","clinical_significance":[]},{"source":"dbSNP","start":140468424,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140468424,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1288076017"},{"start":140468427,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140468427,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794830597","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794830646","clinical_significance":[],"alleles":["C","G","T"],"end":140468428,"strand":1,"feature_type":"variation","start":140468428,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1451189291","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468429,"feature_type":"variation","strand":1,"end":140468429,"alleles":["G","A"]},{"alleles":["T","C"],"end":140468431,"feature_type":"variation","strand":1,"source":"dbSNP","start":140468431,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1400116223","seq_region_name":"7"},{"alleles":["C","T"],"end":140468434,"strand":1,"feature_type":"variation","start":140468434,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794830819","clinical_significance":[]},{"seq_region_name":"7","id":"rs867721146","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140468438,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468438,"source":"dbSNP"},{"alleles":["G","A"],"end":140468439,"feature_type":"variation","strand":1,"source":"dbSNP","start":140468439,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794830945"},{"seq_region_name":"7","id":"rs1794831007","clinical_significance":[],"strand":1,"feature_type":"variation","end":140468441,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468441,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs969552370","end":140468443,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140468443,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140468448,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140468448,"strand":1,"feature_type":"variation","id":"rs2130321268","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1794831126","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468448,"feature_type":"variation","strand":1,"alleles":["CCC","CCCC"],"end":140468450},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468449,"feature_type":"variation","strand":1,"end":140468449,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130321298"},{"source":"dbSNP","start":140468452,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140468452,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1055847328","seq_region_name":"7"},{"end":140468453,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140468453,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs894558969"},{"id":"rs1794831304","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140468454,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468454,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1794831361","clinical_significance":[],"end":140468456,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140468456,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794831421","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468457,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140468457},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794831473","source":"dbSNP","start":140468460,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140468460,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs75056805","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468461,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140468461},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140468462,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468462,"source":"dbSNP","seq_region_name":"7","id":"rs1794831575","clinical_significance":[]},{"alleles":["G","A"],"end":140468463,"feature_type":"variation","strand":1,"source":"dbSNP","start":140468463,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794831626"},{"seq_region_name":"7","id":"rs1422747783","clinical_significance":[],"start":140468464,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140468464,"strand":1,"feature_type":"variation"},{"id":"rs78143375","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140468465,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468465,"source":"dbSNP"},{"id":"rs951216132","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140468466,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468466,"source":"dbSNP"},{"clinical_significance":[],"id":"rs77965259","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468467,"feature_type":"variation","strand":1,"end":140468467,"alleles":["G","A"]},{"start":140468469,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140468469,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794831930","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794831988","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468470,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140468470},{"clinical_significance":[],"seq_region_name":"7","id":"rs995641172","source":"dbSNP","start":140468471,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140468471,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468472,"source":"dbSNP","strand":1,"feature_type":"variation","end":140468472,"alleles":["A","G","T"],"id":"rs1471912896","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140468473,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140468473,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1027118032"},{"source":"dbSNP","start":140468474,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140468474,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs565981734"},{"seq_region_name":"7","id":"rs1463394422","clinical_significance":[],"start":140468475,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140468475,"strand":1,"feature_type":"variation"},{"start":140468479,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140468479,"strand":1,"feature_type":"variation","id":"rs181439485","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468480,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140468480,"seq_region_name":"7","id":"rs912515708","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140468482,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468482,"source":"dbSNP","id":"rs1794832458","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130321646","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468482,"feature_type":"variation","strand":1,"alleles":["CC","-"],"end":140468483},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794832510","alleles":["T","C"],"end":140468489,"feature_type":"variation","strand":1,"source":"dbSNP","start":140468489,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140468499,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140468499,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1794832570","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140468503,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468503,"clinical_significance":[],"seq_region_name":"7","id":"rs1244135141"},{"seq_region_name":"7","id":"rs1020270863","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468504,"source":"dbSNP","strand":1,"feature_type":"variation","end":140468504,"alleles":["C","G"]},{"seq_region_name":"7","id":"rs1161821659","clinical_significance":[],"alleles":["T","C"],"end":140468509,"strand":1,"feature_type":"variation","start":140468509,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140468515,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468515,"clinical_significance":[],"seq_region_name":"7","id":"rs943932751"},{"seq_region_name":"7","id":"rs1389570087","clinical_significance":[],"end":140468516,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140468516,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140468517,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","start":140468517,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1794832912","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140468518,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140468518,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1309422358"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140468521,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468521,"clinical_significance":[],"seq_region_name":"7","id":"rs1794833057"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468522,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140468522,"seq_region_name":"7","id":"rs965094991","clinical_significance":[]},{"seq_region_name":"7","id":"rs1326915012","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140468529,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468529,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["T","TT"],"end":140468529,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468529,"source":"dbSNP","seq_region_name":"7","id":"rs1376451168","clinical_significance":[]},{"alleles":["A","G"],"end":140468530,"feature_type":"variation","strand":1,"source":"dbSNP","start":140468530,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1443605100"},{"source":"dbSNP","start":140468531,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140468531,"alleles":["A","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1392856160"},{"end":140468532,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140468532,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1040119847","clinical_significance":[]},{"start":140468534,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140468534,"strand":1,"feature_type":"variation","id":"rs921248561","seq_region_name":"7","clinical_significance":[]},{"id":"rs975070907","seq_region_name":"7","clinical_significance":[],"alleles":["C","G","T"],"end":140468537,"strand":1,"feature_type":"variation","start":140468537,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1410124030","source":"dbSNP","start":140468545,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140468545,"alleles":["G","A","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs947478899","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468546,"source":"dbSNP","strand":1,"feature_type":"variation","end":140468546,"alleles":["C","A","T"]},{"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140468550,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468550,"clinical_significance":[],"seq_region_name":"7","id":"rs1160825119"},{"seq_region_name":"7","id":"rs1043146543","clinical_significance":[],"strand":1,"feature_type":"variation","end":140468551,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468551,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140468554,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468554,"clinical_significance":[],"seq_region_name":"7","id":"rs1237222846"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468556,"source":"dbSNP","strand":1,"feature_type":"variation","end":140468556,"alleles":["C","G","T"],"seq_region_name":"7","id":"rs1193976784","clinical_significance":[]},{"source":"dbSNP","start":140468558,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140468558,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1794833931","seq_region_name":"7"},{"start":140468559,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140468559,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794833997","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794834055","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140468564,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468564},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468564,"feature_type":"variation","strand":1,"alleles":["GG","GGG"],"end":140468565,"clinical_significance":[],"seq_region_name":"7","id":"rs1330332097"},{"seq_region_name":"7","id":"rs1265148276","clinical_significance":[],"end":140468565,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140468565,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1794834211","clinical_significance":[],"end":140468568,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140468568,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1794834271","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140468569,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468569,"source":"dbSNP"},{"start":140468570,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C","T"],"end":140468570,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs903263132","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140468571,"alleles":["C","A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468571,"clinical_significance":[],"seq_region_name":"7","id":"rs921048070"},{"alleles":["A","G"],"end":140468572,"strand":1,"feature_type":"variation","start":140468572,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794834484","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794834546","source":"dbSNP","start":140468573,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A","G"],"end":140468573,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1057228472","clinical_significance":[],"end":140468575,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140468575,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468578,"feature_type":"variation","strand":1,"end":140468578,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794834613"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468579,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140468579,"seq_region_name":"7","id":"rs1238057716","clinical_significance":[]},{"alleles":["A","T"],"end":140468580,"feature_type":"variation","strand":1,"source":"dbSNP","start":140468580,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794834711"},{"source":"dbSNP","start":140468582,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140468582,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs896058776"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468583,"feature_type":"variation","strand":1,"alleles":["C","A","G"],"end":140468583,"clinical_significance":[],"seq_region_name":"7","id":"rs1794834774"},{"source":"dbSNP","start":140468584,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140468584,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs536441973","seq_region_name":"7"},{"source":"dbSNP","start":140468585,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140468585,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1236924950"},{"end":140468587,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140468587,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1293895724"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468588,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140468588,"seq_region_name":"7","id":"rs1794835040","clinical_significance":[]},{"seq_region_name":"7","id":"rs1323470283","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468589,"source":"dbSNP","strand":1,"feature_type":"variation","end":140468589,"alleles":["T","C"]},{"feature_type":"variation","strand":1,"end":140468592,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468592,"clinical_significance":[],"seq_region_name":"7","id":"rs1023734550"},{"source":"dbSNP","start":140468593,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140468593,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1387783598"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468593,"feature_type":"variation","strand":1,"alleles":["CCG","CCGAGGTTGCCG"],"end":140468595,"clinical_significance":[],"seq_region_name":"7","id":"rs1010951800"},{"clinical_significance":[],"id":"rs989315172","seq_region_name":"7","alleles":["C","G","T"],"end":140468594,"feature_type":"variation","strand":1,"source":"dbSNP","start":140468594,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs757997807","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468595,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140468595},{"end":140468599,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140468599,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1379282897","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794835485","feature_type":"variation","strand":1,"end":140468600,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468600},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130322512","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468601,"feature_type":"variation","strand":1,"end":140468601,"alleles":["T","C"]},{"clinical_significance":[],"id":"rs1794835536","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468603,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140468603},{"feature_type":"variation","strand":1,"end":140468605,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468605,"clinical_significance":[],"seq_region_name":"7","id":"rs186268067"},{"clinical_significance":[],"id":"rs1026762133","seq_region_name":"7","alleles":["C","T"],"end":140468606,"feature_type":"variation","strand":1,"source":"dbSNP","start":140468606,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140468607,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140468611,"alleles":["AGGAG","AG"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1375781144","clinical_significance":[]},{"seq_region_name":"7","id":"rs1197927162","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468609,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140468609},{"end":140468611,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140468611,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1794835736","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1046334850","feature_type":"variation","strand":1,"end":140468614,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468614},{"end":140468615,"alleles":["T","C","G"],"strand":1,"feature_type":"variation","start":140468615,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs927868923","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794835936","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140468616,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468616},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468618,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140468618,"clinical_significance":[],"seq_region_name":"7","id":"rs2130322642"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1214477247","end":140468619,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140468619,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1488031096","alleles":["G","C","T"],"end":140468626,"feature_type":"variation","strand":1,"source":"dbSNP","start":140468626,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["G","A","T"],"end":140468628,"strand":1,"feature_type":"variation","start":140468628,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs938720385","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468631,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140468631,"clinical_significance":[],"seq_region_name":"7","id":"rs1585485283"},{"clinical_significance":[],"id":"rs1055689938","seq_region_name":"7","source":"dbSNP","start":140468632,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","G","T"],"end":140468632,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs894569042","seq_region_name":"7","end":140468633,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140468633,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794836337","source":"dbSNP","start":140468633,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["GG","G"],"end":140468634,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468638,"feature_type":"variation","strand":1,"alleles":["T","A","C","G"],"end":140468638,"clinical_significance":[],"seq_region_name":"7","id":"rs779488455"},{"clinical_significance":[],"seq_region_name":"7","id":"rs541889503","end":140468642,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140468642,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468643,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140468643,"seq_region_name":"7","id":"rs560402278","clinical_significance":[]},{"seq_region_name":"7","id":"rs1049050545","clinical_significance":[],"strand":1,"feature_type":"variation","end":140468647,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468647,"source":"dbSNP"},{"end":140468648,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140468648,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130322851"},{"seq_region_name":"7","id":"rs1397551940","clinical_significance":[],"alleles":["G","A"],"end":140468652,"strand":1,"feature_type":"variation","start":140468652,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794836601","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140468655,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468655},{"source":"dbSNP","start":140468656,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140468656,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1258909238","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1794836708","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468662,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140468662},{"start":140468663,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140468663,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794836752","clinical_significance":[]},{"clinical_significance":[],"id":"rs1313094015","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468666,"feature_type":"variation","strand":1,"end":140468693,"alleles":["ACTCCAACCTGGCGACAGACTGAGACTC","ACTC"]},{"end":140468669,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140468669,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794836857"},{"strand":1,"feature_type":"variation","end":140468670,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468670,"source":"dbSNP","seq_region_name":"7","id":"rs1415760117","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140468672,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468672,"clinical_significance":[],"seq_region_name":"7","id":"rs887309529"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468673,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140468673,"clinical_significance":[],"seq_region_name":"7","id":"rs1794836999"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468675,"source":"dbSNP","strand":1,"feature_type":"variation","end":140468675,"alleles":["T","G"],"seq_region_name":"7","id":"rs1585485358","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1399620149","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468677,"feature_type":"variation","strand":1,"end":140468677,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs189425176","feature_type":"variation","strand":1,"end":140468678,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468678},{"end":140468679,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140468679,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1019903155"},{"id":"rs1185886638","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","AA"],"end":140468680,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468680,"source":"dbSNP"},{"source":"dbSNP","start":140468684,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140468684,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs965610831","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs996520887","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468687,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140468687},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794837440","feature_type":"variation","strand":1,"end":140468690,"alleles":["GAGA","GA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468687},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140468689,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468689,"clinical_significance":[],"seq_region_name":"7","id":"rs1258389845"},{"feature_type":"variation","strand":1,"alleles":["CTCT","CT"],"end":140468694,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468691,"clinical_significance":[],"seq_region_name":"7","id":"rs1794837537"},{"clinical_significance":[],"id":"rs1794837595","seq_region_name":"7","source":"dbSNP","start":140468693,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140468693,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140468695,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468695,"source":"dbSNP","seq_region_name":"7","id":"rs2130323165","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140468697,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468697,"source":"dbSNP","id":"rs2130323173","seq_region_name":"7","clinical_significance":[]},{"id":"rs1585485403","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140468698,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468698,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1343479452","seq_region_name":"7","alleles":["C","A","G"],"end":140468699,"feature_type":"variation","strand":1,"source":"dbSNP","start":140468699,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794837755","source":"dbSNP","start":140468699,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["CACA","CA","CACACA"],"end":140468702,"feature_type":"variation","strand":1},{"id":"rs4725701","seq_region_name":"7","clinical_significance":[],"start":140468700,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140468700,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1794837852","clinical_significance":[],"start":140468700,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","AA","AAAAAAA"],"end":140468700,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140468701,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468701,"source":"dbSNP","id":"rs1207819561","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794837984","clinical_significance":[],"strand":1,"feature_type":"variation","end":140468701,"alleles":["C","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468701,"source":"dbSNP"},{"start":140468702,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140468702,"alleles":["A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1475928879","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468702,"source":"dbSNP","strand":1,"feature_type":"variation","end":140468725,"alleles":["AAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAA","AAAAAAAAAAAAA","AAAAAAAAAAAAAA","AAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA"],"seq_region_name":"7","id":"rs528725182","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1491138580","feature_type":"variation","strand":1,"alleles":["-","C","G"],"end":140468702,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468703},{"clinical_significance":[],"id":"rs975336027","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468703,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140468703},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794838737","feature_type":"variation","strand":1,"alleles":["-","T"],"end":140468705,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468706},{"source":"dbSNP","start":140468709,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["-","G"],"end":140468708,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794838789"},{"source":"dbSNP","start":140468710,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140468710,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1198410897"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1428623923","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468713,"feature_type":"variation","strand":1,"alleles":["AAAAAAAAAA","AAAAAAAAAAGAAAAAAAAAA"],"end":140468722},{"end":140468714,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140468714,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1027953225","clinical_significance":[]},{"seq_region_name":"7","id":"rs957792384","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468716,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140468716},{"start":140468718,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AAAAAAAA","AAAAAAAAAAAAAAAAAAATAAAAAAAA"],"end":140468725,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794838924","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468719,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140468719,"clinical_significance":[],"id":"rs1275627071","seq_region_name":"7"},{"start":140468719,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140468725,"alleles":["AAAAAAA","AAAAAAAAAAAAAACAAAAAAA"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794839033","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468719,"source":"dbSNP","strand":1,"feature_type":"variation","end":140468727,"alleles":["AAAAAAAGA","A"],"id":"rs1312885946","seq_region_name":"7","clinical_significance":[]},{"end":140468725,"alleles":["AAAA","AAAAAAAAAAAAACAAAA"],"strand":1,"feature_type":"variation","start":140468722,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794839148","clinical_significance":[]},{"end":140468729,"alleles":["AAAAGACA","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140468722,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794839203"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468723,"source":"dbSNP","strand":1,"feature_type":"variation","end":140468725,"alleles":["AAA","AAAAAAAAAAAACAAA"],"seq_region_name":"7","id":"rs1794839252","clinical_significance":[]},{"clinical_significance":[],"id":"rs1229519822","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140468725,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468725},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468725,"feature_type":"variation","strand":1,"end":140468725,"alleles":["A","AAAAAAAAAAATA","AAAAAAAAAACA","AAAAAAAAACA","AAAAAAAAACACA"],"clinical_significance":[],"id":"rs1794839341","seq_region_name":"7"},{"start":140468726,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140468726,"strand":1,"feature_type":"variation","id":"rs989274482","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140468726,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["GAC","-"],"end":140468728,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130323720"},{"alleles":["A","T"],"end":140468727,"feature_type":"variation","strand":1,"source":"dbSNP","start":140468727,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1394171786","seq_region_name":"7"},{"source":"dbSNP","start":140468728,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["-","AAAAAAAAAC"],"end":140468727,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130323749"},{"feature_type":"variation","strand":1,"end":140468728,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468728,"clinical_significance":[],"seq_region_name":"7","id":"rs1311785920"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468729,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140468729,"seq_region_name":"7","id":"rs1794839654","clinical_significance":[]},{"end":140468730,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140468730,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794839699","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794839756","clinical_significance":[],"start":140468732,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140468732,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1283234131","seq_region_name":"7","feature_type":"variation","strand":1,"end":140468734,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468734},{"start":140468734,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TGGTGG","TGG"],"end":140468739,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794839853","clinical_significance":[]},{"source":"dbSNP","start":140468735,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140468735,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794839921"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1052071198","source":"dbSNP","start":140468737,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140468737,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1442564545","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468738,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140468738},{"id":"rs1794840059","seq_region_name":"7","clinical_significance":[],"alleles":["GAGAG","GAG"],"end":140468743,"strand":1,"feature_type":"variation","start":140468739,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140468741,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140468741,"alleles":["G","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794840116","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468747,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140468747,"clinical_significance":[],"seq_region_name":"7","id":"rs1794840173"},{"seq_region_name":"7","id":"rs1794840230","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468750,"source":"dbSNP","strand":1,"feature_type":"variation","end":140468755,"alleles":["AATAAT","AAT"]},{"end":140468752,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140468752,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1378675699"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468756,"feature_type":"variation","strand":1,"end":140468756,"alleles":["G","T"],"clinical_significance":[],"id":"rs2130323987","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794840327","feature_type":"variation","strand":1,"end":140468758,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468758},{"source":"dbSNP","start":140468760,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140468760,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794840381"},{"seq_region_name":"7","id":"rs1794840448","clinical_significance":[],"strand":1,"feature_type":"variation","end":140468761,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468761,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1328964991","end":140468765,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140468765,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["T","G"],"end":140468769,"feature_type":"variation","strand":1,"source":"dbSNP","start":140468769,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1021105328"},{"source":"dbSNP","start":140468771,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140468771,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794840623"},{"source":"dbSNP","start":140468772,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140468772,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1445804068"},{"seq_region_name":"7","id":"rs921164435","clinical_significance":[],"start":140468775,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140468775,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794840782","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468776,"feature_type":"variation","strand":1,"end":140468776,"alleles":["C","T"]},{"clinical_significance":[],"id":"rs548715066","seq_region_name":"7","end":140468777,"alleles":["CT","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140468776,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1403670461","source":"dbSNP","start":140468777,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140468777,"feature_type":"variation","strand":1},{"id":"rs2130324162","seq_region_name":"7","clinical_significance":[],"start":140468783,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140468783,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"alleles":["AATAAT","AATAATAAT"],"end":140468791,"feature_type":"variation","strand":1,"source":"dbSNP","start":140468786,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794840945"},{"id":"rs1229306044","seq_region_name":"7","clinical_significance":[],"end":140468788,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","start":140468788,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140468796,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468796,"clinical_significance":[],"id":"rs1413236316","seq_region_name":"7"},{"alleles":["T","C"],"end":140468804,"feature_type":"variation","strand":1,"source":"dbSNP","start":140468804,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1794841114","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1159230199","clinical_significance":[],"end":140468805,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140468805,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140468809,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140468809,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs2130324256","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468812,"feature_type":"variation","strand":1,"end":140468812,"alleles":["G","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs113221534"},{"clinical_significance":[],"seq_region_name":"7","id":"rs552462509","source":"dbSNP","start":140468814,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140468814,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs982347330","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140468819,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468819,"source":"dbSNP"},{"end":140468822,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140468822,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs746549500","seq_region_name":"7"},{"alleles":["A","G"],"end":140468824,"feature_type":"variation","strand":1,"source":"dbSNP","start":140468824,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs937892972","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468825,"feature_type":"variation","strand":1,"end":140468825,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794841557"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140468828,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468828,"clinical_significance":[],"seq_region_name":"7","id":"rs2130324344"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140468830,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468830,"source":"dbSNP","seq_region_name":"7","id":"rs991469734","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140468831,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468831,"source":"dbSNP","seq_region_name":"7","id":"rs1227767945","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1340293644","feature_type":"variation","strand":1,"alleles":["AAA","AA"],"end":140468833,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468831},{"feature_type":"variation","strand":1,"end":140468836,"alleles":["AACAA","AA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468832,"clinical_significance":[],"id":"rs1794841757","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1255412353","feature_type":"variation","strand":1,"end":140468834,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468834},{"clinical_significance":[],"seq_region_name":"7","id":"rs1220094333","feature_type":"variation","strand":1,"alleles":["AAA","A"],"end":140468837,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468835},{"clinical_significance":[],"id":"rs10258350","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140468839,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468839},{"feature_type":"variation","strand":1,"end":140468844,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468844,"clinical_significance":[],"seq_region_name":"7","id":"rs781651241"},{"alleles":["T","C","G"],"end":140468845,"strand":1,"feature_type":"variation","start":140468845,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1223857630","clinical_significance":[]},{"seq_region_name":"7","id":"rs182523545","clinical_significance":[],"strand":1,"feature_type":"variation","end":140468846,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468846,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794842198","end":140468853,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140468853,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468859,"feature_type":"variation","strand":1,"end":140468859,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs934707612"},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140468861,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468861,"source":"dbSNP","id":"rs1794842302","seq_region_name":"7","clinical_significance":[]},{"start":140468866,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140468866,"strand":1,"feature_type":"variation","id":"rs1057236744","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["ACACA","ACA"],"end":140468871,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468867,"source":"dbSNP","seq_region_name":"7","id":"rs1199203529","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468868,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140468868,"seq_region_name":"7","id":"rs2130324602","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1048494605","source":"dbSNP","start":140468870,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140468870,"alleles":["C","G","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794842488","feature_type":"variation","strand":1,"end":140468871,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468871},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468872,"source":"dbSNP","strand":1,"feature_type":"variation","end":140468872,"alleles":["G","A"],"seq_region_name":"7","id":"rs1585485710","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794842603","alleles":["T","C"],"end":140468873,"feature_type":"variation","strand":1,"source":"dbSNP","start":140468873,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468875,"source":"dbSNP","strand":1,"feature_type":"variation","end":140468875,"alleles":["A","C"],"id":"rs2130324669","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794842669","clinical_significance":[],"strand":1,"feature_type":"variation","end":140468880,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468880,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794842718","end":140468885,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140468885,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140468887,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468887,"source":"dbSNP","id":"rs1794842783","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468887,"feature_type":"variation","strand":1,"end":140468892,"alleles":["TCTTCT","TCT"],"clinical_significance":[],"seq_region_name":"7","id":"rs1256042458"},{"strand":1,"feature_type":"variation","alleles":["TCTCT","TCT"],"end":140468894,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468890,"source":"dbSNP","seq_region_name":"7","id":"rs1794842894","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140468892,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468892,"source":"dbSNP","seq_region_name":"7","id":"rs550631625","clinical_significance":[]},{"end":140468893,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140468893,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794843010","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1295203546","alleles":["C","G"],"end":140468897,"feature_type":"variation","strand":1,"source":"dbSNP","start":140468897,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468898,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140468898,"clinical_significance":[],"id":"rs1434133823","seq_region_name":"7"},{"source":"dbSNP","start":140468901,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140468901,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794843170"},{"alleles":["C","G"],"end":140468906,"strand":1,"feature_type":"variation","start":140468906,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs895954746","clinical_significance":[]},{"source":"dbSNP","start":140468911,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140468911,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1319015248","seq_region_name":"7"},{"seq_region_name":"7","id":"rs887186484","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468915,"source":"dbSNP","strand":1,"feature_type":"variation","end":140468915,"alleles":["C","G"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468918,"feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140468918,"clinical_significance":[],"id":"rs1585485751","seq_region_name":"7"},{"clinical_significance":[],"id":"rs34594147","seq_region_name":"7","end":140468919,"alleles":["TT","T","TTT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140468918,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1794843786","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468919,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140468919},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794843843","end":140468924,"alleles":["TAATAA","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140468919,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs200345550","feature_type":"variation","strand":1,"alleles":["AA","A"],"end":140468921,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468920},{"clinical_significance":[],"id":"rs1794843942","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468921,"feature_type":"variation","strand":1,"alleles":["-","T"],"end":140468920},{"source":"dbSNP","start":140468922,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140468922,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1378679400","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140468923,"alleles":["-","TT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468924,"clinical_significance":[],"id":"rs1195777660","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794844099","source":"dbSNP","start":140468926,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140468926,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140468931,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468931,"source":"dbSNP","id":"rs1794844153","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","G"],"end":140468932,"strand":1,"feature_type":"variation","start":140468932,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1794844203","seq_region_name":"7","clinical_significance":[]},{"start":140468940,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140468940,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1044674938","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794844391","clinical_significance":[],"start":140468945,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140468945,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"alleles":["A","C"],"end":140468946,"feature_type":"variation","strand":1,"source":"dbSNP","start":140468946,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794844477"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468947,"source":"dbSNP","strand":1,"feature_type":"variation","end":140468947,"alleles":["T","C"],"seq_region_name":"7","id":"rs1387943564","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585485795","feature_type":"variation","strand":1,"end":140468949,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468949},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794844720","source":"dbSNP","start":140468954,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140468954,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1794844810","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468955,"source":"dbSNP","strand":1,"feature_type":"variation","end":140468955,"alleles":["C","G"]},{"clinical_significance":[],"id":"rs1585485806","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468958,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140468958},{"alleles":["C","T"],"end":140468960,"strand":1,"feature_type":"variation","start":140468960,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794844990","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1448445853","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468964,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140468964},{"id":"rs1794845187","seq_region_name":"7","clinical_significance":[],"alleles":["AATAAT","AAT"],"end":140468970,"strand":1,"feature_type":"variation","start":140468965,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1794845279","clinical_significance":[],"end":140468966,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140468966,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140468967,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468967,"source":"dbSNP","seq_region_name":"7","id":"rs1173744893","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794845452","clinical_significance":[],"start":140468971,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140468971,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140468974,"source":"dbSNP","strand":1,"feature_type":"variation","end":140468974,"alleles":["A","-"],"seq_region_name":"7","id":"rs779942925","clinical_significance":[]},{"source":"dbSNP","start":140468976,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140468976,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs748266478"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794845690","alleles":["G","A"],"end":140468981,"feature_type":"variation","strand":1,"source":"dbSNP","start":140468981,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140468984,"feature_type":"variation","strand":1,"end":140468984,"alleles":["C","T"],"clinical_significance":[],"id":"rs185865956","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1396326580","end":140468988,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140468988,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140468989,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140468989,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794845929"},{"source":"dbSNP","start":140468996,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140468996,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1454980280"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469000,"source":"dbSNP","strand":1,"feature_type":"variation","end":140469000,"alleles":["T","A"],"seq_region_name":"7","id":"rs1794846027","clinical_significance":[]},{"seq_region_name":"7","id":"rs940235834","clinical_significance":[],"end":140469006,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140469006,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1794846129","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469008,"feature_type":"variation","strand":1,"end":140469008,"alleles":["A","C"]},{"strand":1,"feature_type":"variation","end":140469010,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469010,"source":"dbSNP","id":"rs1794846180","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1189856946","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["ACA","A"],"end":140469013,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469011,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs529684047","feature_type":"variation","strand":1,"end":140469025,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469025},{"start":140469029,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140469029,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794846334","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130325375","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469037,"source":"dbSNP","strand":1,"feature_type":"variation","end":140469037,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1243230823","clinical_significance":[],"end":140469040,"alleles":["C","-"],"strand":1,"feature_type":"variation","start":140469040,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140469041,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TAT","T"],"end":140469043,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1216675225","clinical_significance":[]},{"end":140469042,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140469042,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794846451"},{"source":"dbSNP","start":140469043,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140469043,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs144416485","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1489007524","clinical_significance":[],"start":140469046,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140469046,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140469052,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140469052,"alleles":["C","A","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs537870370"},{"id":"rs1794846721","seq_region_name":"7","clinical_significance":[],"start":140469057,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140469057,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469059,"feature_type":"variation","strand":1,"end":140469059,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794846774"},{"feature_type":"variation","strand":1,"end":140469062,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469062,"clinical_significance":[],"seq_region_name":"7","id":"rs1283431858"},{"seq_region_name":"7","id":"rs148397521","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469064,"source":"dbSNP","strand":1,"feature_type":"variation","end":140469064,"alleles":["C","A","T"]},{"source":"dbSNP","start":140469065,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140469065,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs534037868"},{"feature_type":"variation","strand":1,"end":140469066,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469066,"clinical_significance":[],"seq_region_name":"7","id":"rs1794847035"},{"seq_region_name":"7","id":"rs1217292410","clinical_significance":[],"start":140469067,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140469067,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1366755924","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469069,"feature_type":"variation","strand":1,"end":140469069,"alleles":["G","A"]},{"feature_type":"variation","strand":1,"end":140469075,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469075,"clinical_significance":[],"seq_region_name":"7","id":"rs997076729"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469076,"feature_type":"variation","strand":1,"end":140469076,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1401893895"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140469077,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469077,"source":"dbSNP","seq_region_name":"7","id":"rs1358778500","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794847454","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469078,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140469078},{"start":140469083,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140469083,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1383772267","clinical_significance":[]},{"id":"rs1794847584","seq_region_name":"7","clinical_significance":[],"start":140469084,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140469084,"strand":1,"feature_type":"variation"},{"alleles":["G","T"],"end":140469085,"feature_type":"variation","strand":1,"source":"dbSNP","start":140469085,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794847641"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1318219526","end":140469086,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140469086,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469087,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140469087,"seq_region_name":"7","id":"rs1794847754","clinical_significance":[]},{"end":140469089,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140469089,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585485964"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469090,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140469090,"clinical_significance":[],"id":"rs1794847868","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140469091,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469091,"source":"dbSNP","seq_region_name":"7","id":"rs886866439","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469092,"feature_type":"variation","strand":1,"end":140469092,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1563093868"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1363301059","end":140469097,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140469097,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469098,"source":"dbSNP","strand":1,"feature_type":"variation","end":140469098,"alleles":["T","A"],"seq_region_name":"7","id":"rs1794848122","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469099,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140469099,"seq_region_name":"7","id":"rs1003937840","clinical_significance":[]},{"source":"dbSNP","start":140469101,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140469101,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1434583539"},{"seq_region_name":"7","id":"rs1794848394","clinical_significance":[],"start":140469102,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140469102,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"id":"rs1585486000","seq_region_name":"7","clinical_significance":[],"start":140469104,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140469104,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140469105,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140469105,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1585486007","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs11766079","feature_type":"variation","strand":1,"end":140469108,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469108},{"end":140469109,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140469109,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs893499492"},{"seq_region_name":"7","id":"rs570631673","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140469111,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469111,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585486051","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469113,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140469113},{"end":140469118,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140469118,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs975639327"},{"strand":1,"feature_type":"variation","end":140469119,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469119,"source":"dbSNP","id":"rs1257414642","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1207735240","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140469125,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469125,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469129,"source":"dbSNP","strand":1,"feature_type":"variation","end":140469129,"alleles":["A","C","G"],"id":"rs1585486078","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1311436094","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140469130,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469130,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1258630067","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469132,"source":"dbSNP","strand":1,"feature_type":"variation","end":140469132,"alleles":["C","T"]},{"source":"dbSNP","start":140469134,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140469134,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs537673023"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469137,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140469137,"seq_region_name":"7","id":"rs1255997243","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140469140,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469140,"clinical_significance":[],"seq_region_name":"7","id":"rs2130326050"},{"end":140469142,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140469142,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1351945669","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130326078","end":140469143,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140469143,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140469149,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469149,"source":"dbSNP","seq_region_name":"7","id":"rs2130326092","clinical_significance":[]},{"start":140469150,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140469150,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794849340","clinical_significance":[]},{"seq_region_name":"7","id":"rs1277575732","clinical_significance":[],"start":140469151,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140469151,"strand":1,"feature_type":"variation"},{"start":140469153,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140469153,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1210989586","clinical_significance":[]},{"end":140469154,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140469154,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs969038521","clinical_significance":[]},{"end":140469156,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140469156,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs978735758","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140469157,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469157,"source":"dbSNP","seq_region_name":"7","id":"rs1465851820","clinical_significance":[]},{"seq_region_name":"7","id":"rs1355537140","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469158,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140469158},{"id":"rs1794849761","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140469159,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469159,"source":"dbSNP"},{"start":140469160,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G","T"],"end":140469160,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1173288785","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794849808","clinical_significance":[],"alleles":["T","C"],"end":140469168,"strand":1,"feature_type":"variation","start":140469168,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs145943865","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469170,"feature_type":"variation","strand":1,"end":140469170,"alleles":["C","G","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794849973","alleles":["AAAAAA","AAAAAAA"],"end":140469176,"feature_type":"variation","strand":1,"source":"dbSNP","start":140469171,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794850039","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469179,"feature_type":"variation","strand":1,"end":140469179,"alleles":["A","C"]},{"start":140469183,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140469183,"strand":1,"feature_type":"variation","id":"rs1794850119","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469186,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140469186,"clinical_significance":[],"seq_region_name":"7","id":"rs966829206"},{"feature_type":"variation","strand":1,"end":140469187,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469187,"clinical_significance":[],"seq_region_name":"7","id":"rs7786776"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469189,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140469189,"id":"rs917303134","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469192,"feature_type":"variation","strand":1,"end":140469192,"alleles":["G","T"],"clinical_significance":[],"id":"rs1794850587","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1034795320","clinical_significance":[],"alleles":["C","T"],"end":140469194,"strand":1,"feature_type":"variation","start":140469194,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs866926219","clinical_significance":[],"start":140469195,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140469195,"alleles":["G","A","T"],"strand":1,"feature_type":"variation"},{"end":140469196,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140469196,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794850857","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469198,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140469198,"seq_region_name":"7","id":"rs959298399","clinical_significance":[]},{"start":140469199,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140469199,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","id":"rs1431006287","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469200,"source":"dbSNP","strand":1,"feature_type":"variation","end":140469200,"alleles":["C","A","T"],"seq_region_name":"7","id":"rs1563093934","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469204,"source":"dbSNP","strand":1,"feature_type":"variation","end":140469204,"alleles":["T","C"],"id":"rs1315946199","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","C"],"end":140469206,"strand":1,"feature_type":"variation","start":140469206,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1257372131","seq_region_name":"7","clinical_significance":[]},{"start":140469207,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140469207,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1245585167","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1174738215","alleles":["C","T"],"end":140469208,"feature_type":"variation","strand":1,"source":"dbSNP","start":140469208,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs990723626","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469209,"feature_type":"variation","strand":1,"end":140469209,"alleles":["C","T"]},{"id":"rs1794851739","seq_region_name":"7","clinical_significance":[],"end":140469211,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140469211,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1310831513","clinical_significance":[],"start":140469217,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140469217,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs920491809","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469219,"feature_type":"variation","strand":1,"end":140469219,"alleles":["A","G"]},{"alleles":["G","A"],"end":140469220,"feature_type":"variation","strand":1,"source":"dbSNP","start":140469220,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794852008"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140469221,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469221,"clinical_significance":[],"id":"rs948941491","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794852194","source":"dbSNP","start":140469222,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140469222,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1044948367","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140469223,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469223},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794852422","feature_type":"variation","strand":1,"alleles":["A","C","T"],"end":140469228,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469228},{"id":"rs1794852540","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140469233,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469233,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1794852615","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469234,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140469234},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140469235,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469235,"clinical_significance":[],"id":"rs1794852706","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140469236,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469236,"source":"dbSNP","seq_region_name":"7","id":"rs1794852799","clinical_significance":[]},{"alleles":["G","A","C"],"end":140469240,"strand":1,"feature_type":"variation","start":140469240,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1794852872","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794852979","feature_type":"variation","strand":1,"end":140469241,"alleles":["GG","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469240},{"alleles":["C","T"],"end":140469242,"feature_type":"variation","strand":1,"source":"dbSNP","start":140469242,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs190923399"},{"clinical_significance":[],"seq_region_name":"7","id":"rs930842147","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469243,"feature_type":"variation","strand":1,"end":140469243,"alleles":["G","A","C","T"]},{"clinical_significance":[],"id":"rs1455229377","seq_region_name":"7","source":"dbSNP","start":140469244,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A","C"],"end":140469244,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140469246,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AA","A"],"end":140469247,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1337587883"},{"clinical_significance":[],"seq_region_name":"7","id":"rs553702121","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469250,"feature_type":"variation","strand":1,"end":140469250,"alleles":["C","T"]},{"start":140469251,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140469251,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs908631952","clinical_significance":[]},{"id":"rs1441324315","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140469253,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469253,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140469255,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469255,"source":"dbSNP","seq_region_name":"7","id":"rs1794853580","clinical_significance":[]},{"start":140469256,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140469256,"alleles":["G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs572126057","clinical_significance":[]},{"clinical_significance":[],"id":"rs1585486321","seq_region_name":"7","source":"dbSNP","start":140469257,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140469257,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140469258,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469258,"clinical_significance":[],"seq_region_name":"7","id":"rs546061546"},{"strand":1,"feature_type":"variation","end":140469259,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469259,"source":"dbSNP","id":"rs1794853822","seq_region_name":"7","clinical_significance":[]},{"end":140469260,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140469260,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794853887"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794853938","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469262,"feature_type":"variation","strand":1,"end":140469262,"alleles":["C","G"]},{"id":"rs1794853994","seq_region_name":"7","clinical_significance":[],"start":140469265,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140469265,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140469266,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469266,"clinical_significance":[],"seq_region_name":"7","id":"rs143268949"},{"seq_region_name":"7","id":"rs1794854122","clinical_significance":[],"end":140469268,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140469268,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs901312310","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469269,"feature_type":"variation","strand":1,"alleles":["T","A","G"],"end":140469269},{"start":140469278,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140469278,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1456313937","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794854325","clinical_significance":[],"strand":1,"feature_type":"variation","end":140469283,"alleles":["A","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469283,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140469284,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469284,"source":"dbSNP","seq_region_name":"7","id":"rs1336895920","clinical_significance":[]},{"seq_region_name":"7","id":"rs1230734596","clinical_significance":[],"alleles":["C","T"],"end":140469285,"strand":1,"feature_type":"variation","start":140469285,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140469286,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140469286,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130327128"},{"strand":1,"feature_type":"variation","end":140469287,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469287,"source":"dbSNP","seq_region_name":"7","id":"rs1794854523","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs932788982","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140469288,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469288},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469289,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140469289,"seq_region_name":"7","id":"rs1489430003","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130327214","source":"dbSNP","start":140469292,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140469292,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469299,"feature_type":"variation","strand":1,"end":140469299,"alleles":["C","G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs34662984"},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140469301,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469301,"clinical_significance":[],"seq_region_name":"7","id":"rs1266751960"},{"clinical_significance":[],"id":"rs1794854850","seq_region_name":"7","source":"dbSNP","start":140469302,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140469302,"alleles":["G","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1794854910","clinical_significance":[],"start":140469303,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140469303,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794854974","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469305,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140469305},{"source":"dbSNP","start":140469307,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140469307,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs553901436"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794855109","feature_type":"variation","strand":1,"end":140469308,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469308},{"start":140469310,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140469310,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","id":"rs1238387524","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140469311,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469311,"clinical_significance":[],"seq_region_name":"7","id":"rs894056266"},{"alleles":["A","T"],"end":140469312,"strand":1,"feature_type":"variation","start":140469312,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794855281","clinical_significance":[]},{"source":"dbSNP","start":140469313,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140469313,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs182611244"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469314,"source":"dbSNP","strand":1,"feature_type":"variation","end":140469314,"alleles":["A","G"],"seq_region_name":"7","id":"rs1266907967","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469317,"feature_type":"variation","strand":1,"end":140469317,"alleles":["C","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1291250657"},{"end":140469318,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140469318,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794855628"},{"source":"dbSNP","start":140469319,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140469319,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs562602801","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140469320,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469320,"source":"dbSNP","seq_region_name":"7","id":"rs1190135174","clinical_significance":[]},{"alleles":["C","T"],"end":140469321,"feature_type":"variation","strand":1,"source":"dbSNP","start":140469321,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794855912"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1250552955","source":"dbSNP","start":140469322,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140469322,"alleles":["T","A"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140469323,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469323,"clinical_significance":[],"id":"rs906040803","seq_region_name":"7"},{"seq_region_name":"7","id":"rs759021807","clinical_significance":[],"end":140469338,"alleles":["AAAAAAAAAAAAAAA","AAAAAA","AAAAAAAAAAAA","AAAAAAAAAAAAA","AAAAAAAAAAAAAA","AAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAA"],"strand":1,"feature_type":"variation","start":140469324,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469337,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140469337,"seq_region_name":"7","id":"rs1794856494","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794856563","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469339,"feature_type":"variation","strand":1,"end":140469338,"alleles":["-","G"]},{"seq_region_name":"7","id":"rs1010580226","clinical_significance":[],"strand":1,"feature_type":"variation","end":140469339,"alleles":["T","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469339,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469340,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140469340,"clinical_significance":[],"id":"rs996731171","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs7776957","alleles":["T","A","C","G"],"end":140469341,"feature_type":"variation","strand":1,"source":"dbSNP","start":140469341,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140469344,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140469344,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs548316448","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794857162","clinical_significance":[],"alleles":["TAT","T"],"end":140469346,"strand":1,"feature_type":"variation","start":140469344,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1187936473","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469346,"feature_type":"variation","strand":1,"end":140469346,"alleles":["T","C"]},{"source":"dbSNP","start":140469347,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140469347,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs146712871"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469351,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140469351,"clinical_significance":[],"seq_region_name":"7","id":"rs1288424875"},{"clinical_significance":[],"id":"rs1461827141","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140469352,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469352},{"seq_region_name":"7","id":"rs527303737","clinical_significance":[],"alleles":["G","A","C"],"end":140469353,"strand":1,"feature_type":"variation","start":140469353,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469354,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140469354,"seq_region_name":"7","id":"rs1794857722","clinical_significance":[]},{"alleles":["A","G"],"end":140469357,"strand":1,"feature_type":"variation","start":140469357,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs978619653","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs902279581","alleles":["T","C"],"end":140469361,"feature_type":"variation","strand":1,"source":"dbSNP","start":140469361,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469362,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140469362,"seq_region_name":"7","id":"rs1329807935","clinical_significance":[]},{"source":"dbSNP","start":140469366,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140469367,"alleles":["CC","CCC"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1301245672"},{"id":"rs1403766142","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140469367,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469367,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs370307259","source":"dbSNP","start":140469368,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140469368,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794858343","feature_type":"variation","strand":1,"alleles":["TAGTGGTTTA","TA"],"end":140469382,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469373},{"feature_type":"variation","strand":1,"alleles":["G","-"],"end":140469375,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469375,"clinical_significance":[],"id":"rs1299512015","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140469376,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469376,"source":"dbSNP","seq_region_name":"7","id":"rs1417406024","clinical_significance":[]},{"alleles":["G","C"],"end":140469378,"strand":1,"feature_type":"variation","start":140469378,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1359531794","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794858576","alleles":["A","G"],"end":140469384,"feature_type":"variation","strand":1,"source":"dbSNP","start":140469384,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469385,"source":"dbSNP","strand":1,"feature_type":"variation","end":140469385,"alleles":["G","A"],"seq_region_name":"7","id":"rs1456541408","clinical_significance":[]},{"seq_region_name":"7","id":"rs1467434468","clinical_significance":[],"start":140469386,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140469387,"alleles":["TA","-"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794858739","source":"dbSNP","start":140469388,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140469388,"feature_type":"variation","strand":1},{"id":"rs1375825279","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469389,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140469389},{"clinical_significance":[],"seq_region_name":"7","id":"rs1034721409","source":"dbSNP","start":140469390,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140469390,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1478183784","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469392,"source":"dbSNP","strand":1,"feature_type":"variation","end":140469392,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1397357403","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469393,"feature_type":"variation","strand":1,"end":140469393,"alleles":["A","C"]},{"seq_region_name":"7","id":"rs1794859046","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140469394,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469394,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469401,"source":"dbSNP","strand":1,"feature_type":"variation","end":140469401,"alleles":["T","C"],"id":"rs1794859103","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1191606502","source":"dbSNP","start":140469402,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140469402,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469404,"source":"dbSNP","strand":1,"feature_type":"variation","end":140469404,"alleles":["A","C"],"seq_region_name":"7","id":"rs771083519","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794859279","clinical_significance":[],"start":140469406,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140469406,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs917372701","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469407,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140469407},{"alleles":["G","A"],"end":140469408,"strand":1,"feature_type":"variation","start":140469408,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs7787217","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469410,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140469410,"seq_region_name":"7","id":"rs1287065261","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469411,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140469411,"clinical_significance":[],"seq_region_name":"7","id":"rs1027561296"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469417,"source":"dbSNP","strand":1,"feature_type":"variation","end":140469417,"alleles":["C","G","T"],"seq_region_name":"7","id":"rs1320627221","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs952020337","end":140469423,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140469423,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1794859807","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469427,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140469427},{"seq_region_name":"7","id":"rs1794859879","clinical_significance":[],"start":140469428,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140469428,"strand":1,"feature_type":"variation"},{"alleles":["A","G"],"end":140469432,"feature_type":"variation","strand":1,"source":"dbSNP","start":140469432,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794859947"},{"clinical_significance":[],"id":"rs1397615363","seq_region_name":"7","alleles":["C","G"],"end":140469436,"feature_type":"variation","strand":1,"source":"dbSNP","start":140469436,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs920724929","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469438,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140469438},{"seq_region_name":"7","id":"rs1794860131","clinical_significance":[],"strand":1,"feature_type":"variation","end":140469440,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469440,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469441,"feature_type":"variation","strand":1,"end":140469441,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794860190"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469442,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140469442,"clinical_significance":[],"seq_region_name":"7","id":"rs1794860249"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1234286042","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469443,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140469443},{"seq_region_name":"7","id":"rs984140565","clinical_significance":[],"start":140469446,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140469446,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1794860420","clinical_significance":[],"end":140469448,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140469448,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140469449,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140469449,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794860479","clinical_significance":[]},{"end":140469451,"alleles":["T","-"],"strand":1,"feature_type":"variation","start":140469451,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs930902297","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585486762","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469454,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140469454},{"clinical_significance":[],"id":"rs1794860649","seq_region_name":"7","feature_type":"variation","strand":1,"end":140469458,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469458},{"seq_region_name":"7","id":"rs1315202766","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["ACTTAGTAACTTAGT","ACTTAGT"],"end":140469473,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469459,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["TAGTA","TA"],"end":140469466,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469462,"source":"dbSNP","seq_region_name":"7","id":"rs1794860758","clinical_significance":[]},{"end":140469463,"alleles":["A","C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140469463,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs908514625"},{"end":140469467,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140469467,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1399868171","clinical_significance":[]},{"id":"rs908113159","seq_region_name":"7","clinical_significance":[],"end":140469470,"alleles":["TT","-"],"strand":1,"feature_type":"variation","start":140469469,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1466020846","seq_region_name":"7","clinical_significance":[],"start":140469471,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140469471,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469472,"feature_type":"variation","strand":1,"end":140469472,"alleles":["G","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs961496580"},{"feature_type":"variation","strand":1,"end":140469475,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469475,"clinical_significance":[],"seq_region_name":"7","id":"rs1168564106"},{"clinical_significance":[],"id":"rs1477565280","seq_region_name":"7","source":"dbSNP","start":140469477,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140469477,"alleles":["G","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs367677273","alleles":["A","C"],"end":140469478,"feature_type":"variation","strand":1,"source":"dbSNP","start":140469478,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140469482,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140469482,"alleles":["A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1220320936","clinical_significance":[]},{"seq_region_name":"7","id":"rs976863303","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140469486,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469486,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1041106606","source":"dbSNP","start":140469489,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140469489,"alleles":["A","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1483778105","clinical_significance":[],"strand":1,"feature_type":"variation","end":140469490,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469490,"source":"dbSNP"},{"alleles":["A","G"],"end":140469492,"strand":1,"feature_type":"variation","start":140469492,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1255826331","clinical_significance":[]},{"seq_region_name":"7","id":"rs900923730","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469495,"source":"dbSNP","strand":1,"feature_type":"variation","end":140469495,"alleles":["G","A","C","T"]},{"seq_region_name":"7","id":"rs538035690","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469496,"source":"dbSNP","strand":1,"feature_type":"variation","end":140469496,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs556131241","clinical_significance":[],"alleles":["A","G"],"end":140469497,"strand":1,"feature_type":"variation","start":140469497,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs996968017","feature_type":"variation","strand":1,"end":140469498,"alleles":["T","C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469498},{"id":"rs1049593925","seq_region_name":"7","clinical_significance":[],"start":140469505,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TCTG","TCTGTCTG"],"end":140469508,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1794861956","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140469508,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469508,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1338256753","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469512,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140469512},{"clinical_significance":[],"seq_region_name":"7","id":"rs932840008","alleles":["G","C"],"end":140469515,"feature_type":"variation","strand":1,"source":"dbSNP","start":140469515,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140469516,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140469516,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794862152"},{"start":140469521,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AAAA","AAA"],"end":140469524,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1475462634","clinical_significance":[]},{"end":140469527,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140469527,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1246464332","clinical_significance":[]},{"end":140469529,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140469529,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794862323","clinical_significance":[]},{"seq_region_name":"7","id":"rs1338343381","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469530,"source":"dbSNP","strand":1,"feature_type":"variation","end":140469530,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1049890281","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140469537,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469537},{"clinical_significance":[],"seq_region_name":"7","id":"rs915501372","source":"dbSNP","start":140469538,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140469538,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469545,"feature_type":"variation","strand":1,"end":140469551,"alleles":["CCTCCTC","CCTC"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794862566"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794862646","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469549,"feature_type":"variation","strand":1,"alleles":["CTCT","CT"],"end":140469552},{"start":140469552,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140469555,"alleles":["TGTT","-"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794862696","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794862755","feature_type":"variation","strand":1,"end":140469556,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469556},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469557,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140469557,"clinical_significance":[],"id":"rs1794862799","seq_region_name":"7"},{"source":"dbSNP","start":140469559,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140469559,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs946937553"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469562,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140469562,"clinical_significance":[],"seq_region_name":"7","id":"rs1402342442"},{"clinical_significance":[],"id":"rs1422998121","seq_region_name":"7","source":"dbSNP","start":140469569,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140469569,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469570,"source":"dbSNP","strand":1,"feature_type":"variation","end":140469570,"alleles":["G","A"],"seq_region_name":"7","id":"rs999967680","clinical_significance":[]},{"seq_region_name":"7","id":"rs1414699652","clinical_significance":[],"strand":1,"feature_type":"variation","end":140469573,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469573,"source":"dbSNP"},{"source":"dbSNP","start":140469576,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140469576,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794863304"},{"alleles":["T","C"],"end":140469583,"strand":1,"feature_type":"variation","start":140469583,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794863355","clinical_significance":[]},{"alleles":["C","T"],"end":140469585,"strand":1,"feature_type":"variation","start":140469585,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1042069623","seq_region_name":"7","clinical_significance":[]},{"start":140469586,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140469586,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1165078770","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1031578442","end":140469589,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140469589,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469590,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140469590,"seq_region_name":"7","id":"rs1384871224","clinical_significance":[]},{"start":140469597,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140469597,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1179625624","clinical_significance":[]},{"clinical_significance":[],"id":"rs1794863688","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469598,"feature_type":"variation","strand":1,"end":140469598,"alleles":["A","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs7777404","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469599,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140469599},{"clinical_significance":[],"seq_region_name":"7","id":"rs373906866","feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140469600,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469600},{"alleles":["T","G"],"end":140469602,"feature_type":"variation","strand":1,"source":"dbSNP","start":140469602,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1370499383","seq_region_name":"7"},{"id":"rs1056179476","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140469603,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469603,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140469606,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469606,"clinical_significance":[],"seq_region_name":"7","id":"rs1794864072"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794864122","source":"dbSNP","start":140469612,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140469612,"alleles":["C","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs535546147","end":140469615,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140469615,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469624,"source":"dbSNP","strand":1,"feature_type":"variation","end":140469624,"alleles":["C","T"],"seq_region_name":"7","id":"rs1415881464","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs894888158","feature_type":"variation","strand":1,"end":140469626,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469626},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469629,"source":"dbSNP","strand":1,"feature_type":"variation","end":140469629,"alleles":["T","C"],"seq_region_name":"7","id":"rs1794864471","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794864563","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469631,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140469631},{"seq_region_name":"7","id":"rs1313990343","clinical_significance":[],"start":140469634,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140469634,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794864723","source":"dbSNP","start":140469638,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140469638,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs776174505","feature_type":"variation","strand":1,"end":140469639,"alleles":["G","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469639},{"start":140469639,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["GGGG","GGG"],"end":140469642,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794864875","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs553871830","source":"dbSNP","start":140469640,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140469640,"alleles":["G","A","C"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140469641,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469641,"clinical_significance":[],"seq_region_name":"7","id":"rs185282593"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794864972","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469642,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140469642},{"id":"rs1585487040","seq_region_name":"7","clinical_significance":[],"alleles":["T","G"],"end":140469643,"strand":1,"feature_type":"variation","start":140469643,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs190294147","seq_region_name":"7","clinical_significance":[],"start":140469646,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140469646,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140469650,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469650,"clinical_significance":[],"seq_region_name":"7","id":"rs1014829736"},{"source":"dbSNP","start":140469651,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140469651,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1295932422"},{"seq_region_name":"7","id":"rs1794865538","clinical_significance":[],"strand":1,"feature_type":"variation","end":140469653,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469653,"source":"dbSNP"},{"end":140469655,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140469655,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs961715722","clinical_significance":[]},{"alleles":["C","A"],"end":140469660,"strand":1,"feature_type":"variation","start":140469660,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794865724","clinical_significance":[]},{"start":140469665,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","T"],"end":140469665,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1024686026","clinical_significance":[]},{"start":140469666,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C","T"],"end":140469666,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs182860677","clinical_significance":[]},{"start":140469667,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140469667,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1441912579","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469668,"feature_type":"variation","strand":1,"alleles":["TTT","TT"],"end":140469670,"clinical_significance":[],"id":"rs1585487115","seq_region_name":"7"},{"id":"rs1794866240","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140469669,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469669,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469675,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140469675,"clinical_significance":[],"seq_region_name":"7","id":"rs1794866340"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794866428","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140469676,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469676},{"seq_region_name":"7","id":"rs2130329574","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469678,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AAA","AA"],"end":140469680},{"alleles":["A","T"],"end":140469680,"strand":1,"feature_type":"variation","start":140469680,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs980572862","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140469685,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469685,"source":"dbSNP","id":"rs1794866605","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","A"],"end":140469686,"strand":1,"feature_type":"variation","start":140469686,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs922689929","clinical_significance":[]},{"clinical_significance":[],"id":"rs954072714","seq_region_name":"7","feature_type":"variation","strand":1,"end":140469687,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469687},{"end":140469689,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140469689,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794866764","clinical_significance":[]},{"end":140469699,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140469699,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs985646911","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs915368566","source":"dbSNP","start":140469700,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140469700,"alleles":["C","T"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140469703,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469703,"source":"dbSNP","seq_region_name":"7","id":"rs908165167","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469709,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140469709,"seq_region_name":"7","id":"rs1794867002","clinical_significance":[]},{"alleles":["A","G"],"end":140469712,"strand":1,"feature_type":"variation","start":140469712,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794867081","clinical_significance":[]},{"id":"rs1794867169","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140469713,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469713,"source":"dbSNP"},{"start":140469714,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140469714,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs944902336","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469718,"feature_type":"variation","strand":1,"end":140469718,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1290574437"},{"clinical_significance":[],"id":"rs1216963812","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469720,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140469720},{"start":140469724,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","G"],"end":140469724,"strand":1,"feature_type":"variation","id":"rs1794867973","seq_region_name":"7","clinical_significance":[]},{"start":140469726,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140469726,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1235647295","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585487188","clinical_significance":[],"start":140469730,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140469730,"alleles":["T","C","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1355426833","clinical_significance":[],"start":140469730,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TAGTGAAACCCCGTCTCTACTAAAAATACAAAAGTTAGTG","TAGTG"],"end":140469769,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140469731,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469731,"clinical_significance":[],"seq_region_name":"7","id":"rs1794868365"},{"seq_region_name":"7","id":"rs1283567795","clinical_significance":[],"start":140469732,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140469732,"strand":1,"feature_type":"variation"},{"id":"rs946894701","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140469733,"alleles":["T","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469733,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1276585979","clinical_significance":[],"start":140469734,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140469734,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1434389815","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469738,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140469738},{"clinical_significance":[],"seq_region_name":"7","id":"rs1482840653","feature_type":"variation","strand":1,"end":140469739,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469739},{"end":140469740,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140469740,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs7801933","clinical_significance":[]},{"seq_region_name":"7","id":"rs1298894901","clinical_significance":[],"end":140469741,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140469741,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs796562439","clinical_significance":[],"start":140469742,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140469742,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140469743,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140469743,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794868999"},{"seq_region_name":"7","id":"rs1391018508","clinical_significance":[],"end":140469746,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140469746,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140469748,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469748,"source":"dbSNP","seq_region_name":"7","id":"rs904267950","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585487266","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469751,"source":"dbSNP","strand":1,"feature_type":"variation","end":140469751,"alleles":["A","G"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469756,"source":"dbSNP","strand":1,"feature_type":"variation","end":140469756,"alleles":["T","C"],"seq_region_name":"7","id":"rs1794869245","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140469759,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469759,"source":"dbSNP","id":"rs1794869302","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469759,"feature_type":"variation","strand":1,"alleles":["AAAA","AA"],"end":140469762,"clinical_significance":[],"id":"rs1000019984","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1794869410","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469761,"source":"dbSNP","strand":1,"feature_type":"variation","end":140469761,"alleles":["A","G"]},{"id":"rs1794869463","seq_region_name":"7","clinical_significance":[],"start":140469762,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140469762,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469765,"source":"dbSNP","strand":1,"feature_type":"variation","end":140469765,"alleles":["T","C"],"seq_region_name":"7","id":"rs1052879621","clinical_significance":[]},{"source":"dbSNP","start":140469767,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140469767,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585487294"},{"source":"dbSNP","start":140469768,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140469768,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1794869630","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1794869683","clinical_significance":[],"end":140469770,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140469770,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["G","C"],"end":140469772,"feature_type":"variation","strand":1,"source":"dbSNP","start":140469772,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794869739"},{"seq_region_name":"7","id":"rs1794869784","clinical_significance":[],"start":140469774,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140469774,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1190047546","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140469775,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469775},{"seq_region_name":"7","id":"rs1794869922","clinical_significance":[],"start":140469776,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140469776,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140469777,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469777,"source":"dbSNP","seq_region_name":"7","id":"rs1563094223","clinical_significance":[]},{"seq_region_name":"7","id":"rs116896510","clinical_significance":[],"end":140469778,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140469778,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs149956625","clinical_significance":[],"end":140469780,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140469780,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs939047482","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140469781,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469781,"source":"dbSNP"},{"seq_region_name":"7","id":"rs565167444","clinical_significance":[],"start":140469783,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140469783,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1214769073","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469784,"source":"dbSNP","strand":1,"feature_type":"variation","end":140469784,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs187492660","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469785,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140469785},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469786,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140469786,"clinical_significance":[],"seq_region_name":"7","id":"rs970488025"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469787,"feature_type":"variation","strand":1,"end":140469787,"alleles":["G","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs562103836"},{"seq_region_name":"7","id":"rs1278881471","clinical_significance":[],"start":140469790,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140469790,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs894899520","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469791,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140469791},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140469792,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469792,"clinical_significance":[],"seq_region_name":"7","id":"rs1338690848"},{"seq_region_name":"7","id":"rs1288556400","clinical_significance":[],"start":140469796,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140469796,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"start":140469801,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140469801,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1001532658","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140469801,"alleles":["A","AA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469801,"source":"dbSNP","seq_region_name":"7","id":"rs2130330418","clinical_significance":[]},{"start":140469802,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G","T"],"end":140469802,"strand":1,"feature_type":"variation","id":"rs1361321604","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1011926933","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469803,"feature_type":"variation","strand":1,"end":140469803,"alleles":["A","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1170300719","feature_type":"variation","strand":1,"end":140469812,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469812},{"source":"dbSNP","start":140469813,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140469813,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1375703984"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469814,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140469814,"clinical_significance":[],"seq_region_name":"7","id":"rs1465754154"},{"end":140469814,"alleles":["-","G"],"strand":1,"feature_type":"variation","start":140469815,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794871232","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1303571194","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469815,"feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140469815},{"source":"dbSNP","start":140469816,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140469816,"alleles":["T","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1048894317"},{"source":"dbSNP","start":140469817,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140469817,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1433060196","seq_region_name":"7"},{"id":"rs1319964492","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140469818,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469818,"source":"dbSNP"},{"start":140469819,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["-","CTCATGCCTACAATCCCAGCCTCCCAA","CTCATGCCTACAATCCCAGCCTCCCCA"],"end":140469818,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794871526","clinical_significance":[]},{"alleles":["G","GCTCATGCCTACAATCCCAGCCTCCCAAG","GCTCATGCCTACAATCCCAGCCTCCCCAG"],"end":140469819,"strand":1,"feature_type":"variation","start":140469819,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1170746567","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1447768892","source":"dbSNP","start":140469819,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140469819,"feature_type":"variation","strand":1},{"id":"rs59578412","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469826,"source":"dbSNP","strand":1,"feature_type":"variation","end":140469826,"alleles":["G","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794872931","source":"dbSNP","start":140469832,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140469832,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794872983","end":140469835,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140469835,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1794873052","seq_region_name":"7","clinical_significance":[],"end":140469838,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140469838,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140469843,"alleles":["AGGAG","AG"],"strand":1,"feature_type":"variation","start":140469839,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794873113","clinical_significance":[]},{"start":140469840,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140469840,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1813321322","clinical_significance":[]},{"id":"rs952106332","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469841,"source":"dbSNP","strand":1,"feature_type":"variation","end":140469841,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1238918126","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469843,"source":"dbSNP","strand":1,"feature_type":"variation","end":140469843,"alleles":["G","A"]},{"alleles":["A","T"],"end":140469844,"feature_type":"variation","strand":1,"source":"dbSNP","start":140469844,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs193062946"},{"seq_region_name":"7","id":"rs1794873391","clinical_significance":[],"start":140469851,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140469851,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469852,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140469852,"clinical_significance":[],"seq_region_name":"7","id":"rs1432392803"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469855,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140469855,"id":"rs1460780245","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","G"],"end":140469856,"strand":1,"feature_type":"variation","start":140469856,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1258691208","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140469857,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469857,"source":"dbSNP","id":"rs1585487556","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140469866,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469866,"clinical_significance":[],"seq_region_name":"7","id":"rs1296380411"},{"end":140469875,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140469875,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794873764","clinical_significance":[]},{"source":"dbSNP","start":140469879,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140469879,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs560315047"},{"seq_region_name":"7","id":"rs908009161","clinical_significance":[],"alleles":["T","A"],"end":140469882,"strand":1,"feature_type":"variation","start":140469882,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140469885,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469885,"source":"dbSNP","id":"rs1316214429","seq_region_name":"7","clinical_significance":[]},{"start":140469893,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140469893,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794874004","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469900,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140469900,"clinical_significance":[],"id":"rs1794874056","seq_region_name":"7"},{"clinical_significance":[],"id":"rs966333782","seq_region_name":"7","source":"dbSNP","start":140469902,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140469902,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs976715807","end":140469903,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140469903,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140469904,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140469904,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs901726458"},{"clinical_significance":[],"seq_region_name":"7","id":"rs55780162","source":"dbSNP","start":140469906,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C","G"],"end":140469906,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469907,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140469907,"clinical_significance":[],"seq_region_name":"7","id":"rs1029646566"},{"seq_region_name":"7","id":"rs1220443563","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469909,"source":"dbSNP","strand":1,"feature_type":"variation","end":140469909,"alleles":["G","A"]},{"start":140469911,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140469911,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs954125101","clinical_significance":[]},{"alleles":["C","T"],"end":140469913,"strand":1,"feature_type":"variation","start":140469913,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1401619335","clinical_significance":[]},{"clinical_significance":[],"id":"rs985135180","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469914,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140469914},{"seq_region_name":"7","id":"rs1585487651","clinical_significance":[],"start":140469916,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140469916,"alleles":["T","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs985573494","clinical_significance":[],"start":140469917,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140469917,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140469920,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140469920,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794874802"},{"seq_region_name":"7","id":"rs183951959","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469929,"source":"dbSNP","strand":1,"feature_type":"variation","end":140469929,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs968658044","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469930,"feature_type":"variation","strand":1,"end":140469930,"alleles":["C","G"]},{"seq_region_name":"7","id":"rs1370781530","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469932,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140469932},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469940,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140469940,"clinical_significance":[],"seq_region_name":"7","id":"rs1794875065"},{"clinical_significance":[],"seq_region_name":"7","id":"rs978274676","alleles":["G","A","C"],"end":140469941,"feature_type":"variation","strand":1,"source":"dbSNP","start":140469941,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140469947,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469947,"clinical_significance":[],"seq_region_name":"7","id":"rs1794875229"},{"id":"rs1585487701","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469948,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140469948},{"source":"dbSNP","start":140469951,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140469951,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1415542286"},{"clinical_significance":[],"id":"rs1181506434","seq_region_name":"7","source":"dbSNP","start":140469953,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140469953,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs543863255","alleles":["G","A"],"end":140469958,"feature_type":"variation","strand":1,"source":"dbSNP","start":140469958,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1238713699","feature_type":"variation","strand":1,"alleles":["AA","A"],"end":140469960,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469959},{"seq_region_name":"7","id":"rs2130331319","clinical_significance":[],"strand":1,"feature_type":"variation","end":140469963,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469963,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140469964,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469964,"source":"dbSNP","id":"rs1794875684","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","C"],"end":140469965,"strand":1,"feature_type":"variation","start":140469965,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1249609243","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1479625777","feature_type":"variation","strand":1,"end":140469967,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140469967},{"seq_region_name":"7","id":"rs2130331379","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469972,"source":"dbSNP","strand":1,"feature_type":"variation","end":140469972,"alleles":["T","C"]},{"end":140469973,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140469973,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130331395","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140469976,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469976,"source":"dbSNP","seq_region_name":"7","id":"rs1794875871","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794875931","clinical_significance":[],"strand":1,"feature_type":"variation","end":140469977,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469977,"source":"dbSNP"},{"source":"dbSNP","start":140469979,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C","G"],"end":140469979,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1250766505"},{"start":140469982,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140469982,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1466444817","clinical_significance":[]},{"start":140469982,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140469982,"alleles":["A","-"],"strand":1,"feature_type":"variation","id":"rs2130331460","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794876113","clinical_significance":[],"strand":1,"feature_type":"variation","end":140469983,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469983,"source":"dbSNP"},{"id":"rs1222446392","seq_region_name":"7","clinical_significance":[],"start":140469985,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C","G"],"end":140469985,"strand":1,"feature_type":"variation"},{"start":140469987,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140469987,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs113944210","clinical_significance":[]},{"end":140469994,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140469994,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1313237520","seq_region_name":"7"},{"alleles":["C","G"],"end":140469995,"feature_type":"variation","strand":1,"source":"dbSNP","start":140469995,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1794876358","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140469995,"alleles":["-","CGAAAT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140469996,"source":"dbSNP","seq_region_name":"7","id":"rs2130331536","clinical_significance":[]},{"source":"dbSNP","start":140469997,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140469997,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs991804100","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470008,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140470008,"clinical_significance":[],"seq_region_name":"7","id":"rs530237435"},{"seq_region_name":"7","id":"rs1247616730","clinical_significance":[],"start":140470010,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140470010,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140470011,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140470011,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs548347803"},{"seq_region_name":"7","id":"rs2130331601","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470012,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140470012},{"seq_region_name":"7","id":"rs1794876648","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["AGCCTGGCGACAGAG","-"],"end":140470032,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470018,"source":"dbSNP"},{"alleles":["G","GG"],"end":140470019,"feature_type":"variation","strand":1,"source":"dbSNP","start":140470019,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794876695"},{"clinical_significance":[],"seq_region_name":"7","id":"rs568135663","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470025,"feature_type":"variation","strand":1,"end":140470025,"alleles":["C","T"]},{"alleles":["G","A"],"end":140470026,"strand":1,"feature_type":"variation","start":140470026,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs867083462","clinical_significance":[]},{"alleles":["G","A"],"end":140470030,"feature_type":"variation","strand":1,"source":"dbSNP","start":140470030,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130331695"},{"alleles":["A","G"],"end":140470031,"strand":1,"feature_type":"variation","start":140470031,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1396448390","clinical_significance":[]},{"alleles":["C","A"],"end":140470033,"feature_type":"variation","strand":1,"source":"dbSNP","start":140470033,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1297057816"},{"seq_region_name":"7","id":"rs1794876988","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470034,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140470034},{"seq_region_name":"7","id":"rs1794877054","clinical_significance":[],"end":140470035,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140470035,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140470036,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["GGCTCTG","G"],"end":140470042,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794877100","clinical_significance":[]},{"end":140470038,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140470038,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1423702078","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140470039,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470039,"clinical_significance":[],"id":"rs1458015847","seq_region_name":"7"},{"end":140470040,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140470040,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1351230507","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470041,"source":"dbSNP","strand":1,"feature_type":"variation","end":140470041,"alleles":["T","C"],"seq_region_name":"7","id":"rs1794877358","clinical_significance":[]},{"clinical_significance":[],"id":"rs2130331810","seq_region_name":"7","feature_type":"variation","strand":1,"end":140470042,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470042},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470043,"source":"dbSNP","strand":1,"feature_type":"variation","end":140470043,"alleles":["T","G"],"seq_region_name":"7","id":"rs1794877405","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470043,"source":"dbSNP","strand":1,"feature_type":"variation","end":140470046,"alleles":["TCTC","TC"],"id":"rs1794877464","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1161359835","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470044,"source":"dbSNP","strand":1,"feature_type":"variation","end":140470044,"alleles":["C","T"]},{"strand":1,"feature_type":"variation","alleles":["T","-"],"end":140470045,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470045,"source":"dbSNP","seq_region_name":"7","id":"rs1794877563","clinical_significance":[]},{"clinical_significance":[],"id":"rs2130331867","seq_region_name":"7","feature_type":"variation","strand":1,"end":140470045,"alleles":["T","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470045},{"seq_region_name":"7","id":"rs1794877625","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470046,"source":"dbSNP","strand":1,"feature_type":"variation","end":140470045,"alleles":["-","A"]},{"seq_region_name":"7","id":"rs1301729145","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470046,"source":"dbSNP","strand":1,"feature_type":"variation","end":140470046,"alleles":["C","A"]},{"end":140470046,"alleles":["C","-"],"strand":1,"feature_type":"variation","start":140470046,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1443771590","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1491426952","source":"dbSNP","start":140470046,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["CA","-"],"end":140470047,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794877862","source":"dbSNP","start":140470046,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["CAA","-"],"end":140470048,"feature_type":"variation","strand":1},{"alleles":["A","C"],"end":140470047,"feature_type":"variation","strand":1,"source":"dbSNP","start":140470047,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs77195178"},{"clinical_significance":[],"id":"rs1794877987","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470047,"feature_type":"variation","strand":1,"end":140470047,"alleles":["A","ATAAA"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs35753653","feature_type":"variation","strand":1,"alleles":["AAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAA","AAAAAAAAAA","AAAAAAAAAAAA","AAAAAAAAAAAAA","AAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAA"],"end":140470071,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470047},{"clinical_significance":[],"id":"rs75539995","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140470048,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470048},{"seq_region_name":"7","id":"rs77519955","clinical_significance":[],"start":140470050,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140470050,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["-","T"],"end":140470050,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470051,"source":"dbSNP","seq_region_name":"7","id":"rs1160415777","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585488014","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470051,"feature_type":"variation","strand":1,"end":140470051,"alleles":["A","T"]},{"strand":1,"feature_type":"variation","alleles":["-","T"],"end":140470051,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470052,"source":"dbSNP","seq_region_name":"7","id":"rs1391340900","clinical_significance":[]},{"seq_region_name":"7","id":"rs1363152604","clinical_significance":[],"start":140470052,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140470052,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"start":140470052,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","ATA"],"end":140470052,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1554449385","clinical_significance":[]},{"seq_region_name":"7","id":"rs1455957377","clinical_significance":[],"end":140470052,"alleles":["-","T"],"strand":1,"feature_type":"variation","start":140470053,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140470053,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140470053,"alleles":["A","T"],"strand":1,"feature_type":"variation","id":"rs947710662","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140470053,"alleles":["A","ATA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470053,"clinical_significance":[],"seq_region_name":"7","id":"rs1794878988"},{"seq_region_name":"7","id":"rs1794879053","clinical_significance":[],"start":140470054,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["-","T"],"end":140470053,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140470054,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140470054,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1049308649"},{"alleles":["A","ATA"],"end":140470054,"feature_type":"variation","strand":1,"source":"dbSNP","start":140470054,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1176777222"},{"source":"dbSNP","start":140470055,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140470054,"alleles":["-","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1266774371"},{"clinical_significance":[],"seq_region_name":"7","id":"rs867990833","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470055,"feature_type":"variation","strand":1,"end":140470055,"alleles":["A","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs74711649","source":"dbSNP","start":140470057,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140470057,"alleles":["A","T"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140470058,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["-","T"],"end":140470057,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1563094402","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470058,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140470058,"seq_region_name":"7","id":"rs76733449","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1265675277","alleles":["A","ATA"],"end":140470058,"feature_type":"variation","strand":1,"source":"dbSNP","start":140470058,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["AA","AATAA"],"end":140470059,"feature_type":"variation","strand":1,"source":"dbSNP","start":140470058,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1554449402"},{"feature_type":"variation","strand":1,"end":140470058,"alleles":["-","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470059,"clinical_significance":[],"seq_region_name":"7","id":"rs56268869"},{"clinical_significance":[],"seq_region_name":"7","id":"rs565550129","feature_type":"variation","strand":1,"end":140470059,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470059},{"seq_region_name":"7","id":"rs1554449407","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470059,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","ATA"],"end":140470059},{"seq_region_name":"7","id":"rs1563094415","clinical_significance":[],"strand":1,"feature_type":"variation","end":140470059,"alleles":["-","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470060,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140470060,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470060,"source":"dbSNP","seq_region_name":"7","id":"rs997404153","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470061,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140470061,"seq_region_name":"7","id":"rs1794880014","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470062,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140470062,"clinical_significance":[],"seq_region_name":"7","id":"rs535295477"},{"strand":1,"feature_type":"variation","end":140470062,"alleles":["-","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470063,"source":"dbSNP","seq_region_name":"7","id":"rs1794880141","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470063,"feature_type":"variation","strand":1,"end":140470063,"alleles":["A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1340711949"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1222626852","feature_type":"variation","strand":1,"alleles":["A","T"],"end":140470064,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470064},{"strand":1,"feature_type":"variation","end":140470065,"alleles":["A","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470065,"source":"dbSNP","seq_region_name":"7","id":"rs1371278552","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140470066,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470066,"source":"dbSNP","seq_region_name":"7","id":"rs1380297241","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794880462","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470067,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140470067},{"start":140470068,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140470068,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1028900044","clinical_significance":[]},{"id":"rs1437988294","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470069,"source":"dbSNP","strand":1,"feature_type":"variation","end":140470068,"alleles":["-","T"]},{"seq_region_name":"7","id":"rs1272511380","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140470069,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470069,"source":"dbSNP"},{"seq_region_name":"7","id":"rs79906306","clinical_significance":[],"end":140470071,"alleles":["A","G","T"],"strand":1,"feature_type":"variation","start":140470071,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs62490445","seq_region_name":"7","clinical_significance":[],"start":140470073,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140470073,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140470074,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470074,"source":"dbSNP","seq_region_name":"7","id":"rs1366844290","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794880898","clinical_significance":[],"start":140470075,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140470075,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470076,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140470076,"clinical_significance":[],"seq_region_name":"7","id":"rs889812411"},{"end":140470077,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140470077,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794881047"},{"seq_region_name":"7","id":"rs1467481941","clinical_significance":[],"strand":1,"feature_type":"variation","end":140470078,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470078,"source":"dbSNP"},{"alleles":["G","T"],"end":140470080,"feature_type":"variation","strand":1,"source":"dbSNP","start":140470080,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs949898110"},{"end":140470081,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140470081,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585488237"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140470082,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470082,"clinical_significance":[],"seq_region_name":"7","id":"rs1794881332"},{"feature_type":"variation","strand":1,"end":140470083,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470083,"clinical_significance":[],"seq_region_name":"7","id":"rs1585488247"},{"end":140470086,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140470086,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1585488255","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140470089,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470089,"source":"dbSNP","seq_region_name":"7","id":"rs1585488264","clinical_significance":[]},{"seq_region_name":"7","id":"rs1175769822","clinical_significance":[],"strand":1,"feature_type":"variation","end":140470091,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470091,"source":"dbSNP"},{"end":140470092,"alleles":["A","C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140470092,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1006890717"},{"seq_region_name":"7","id":"rs1794881731","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470093,"source":"dbSNP","strand":1,"feature_type":"variation","end":140470093,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1305630249","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470098,"source":"dbSNP","strand":1,"feature_type":"variation","end":140470098,"alleles":["G","A"]},{"id":"rs1794881845","seq_region_name":"7","clinical_significance":[],"start":140470099,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140470099,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1585488308","clinical_significance":[],"end":140470102,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","start":140470102,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["T","A","C"],"end":140470105,"strand":1,"feature_type":"variation","start":140470105,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1269906964","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["GCT","GCTGCT"],"end":140470109,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470107,"clinical_significance":[],"seq_region_name":"7","id":"rs1794882067"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794882135","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470109,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140470109},{"seq_region_name":"7","id":"rs1585488321","clinical_significance":[],"alleles":["T","A"],"end":140470112,"strand":1,"feature_type":"variation","start":140470112,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1191379677","source":"dbSNP","start":140470114,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140470114,"alleles":["T","G"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140470117,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470117,"source":"dbSNP","seq_region_name":"7","id":"rs547470611","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470118,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140470118,"clinical_significance":[],"id":"rs570344969","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794882438","end":140470119,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140470119,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470121,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140470121,"seq_region_name":"7","id":"rs1794882492","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470122,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140470122,"clinical_significance":[],"seq_region_name":"7","id":"rs1794882558"},{"seq_region_name":"7","id":"rs978669321","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470123,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140470123},{"seq_region_name":"7","id":"rs1794882679","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470124,"source":"dbSNP","strand":1,"feature_type":"variation","end":140470124,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs565877174","clinical_significance":[],"start":140470125,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140470125,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140470126,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470126,"source":"dbSNP","seq_region_name":"7","id":"rs188851457","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470129,"feature_type":"variation","strand":1,"end":140470129,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1027617571"},{"seq_region_name":"7","id":"rs1794882871","clinical_significance":[],"alleles":["A","G"],"end":140470132,"strand":1,"feature_type":"variation","start":140470132,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794882938","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140470133,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470133},{"seq_region_name":"7","id":"rs1245016587","clinical_significance":[],"start":140470134,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C","G"],"end":140470134,"strand":1,"feature_type":"variation"},{"start":140470136,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140470136,"alleles":["T","A"],"strand":1,"feature_type":"variation","id":"rs1794883062","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1271440838","clinical_significance":[],"strand":1,"feature_type":"variation","end":140470139,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470139,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140470140,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470140,"source":"dbSNP","seq_region_name":"7","id":"rs56059991","clinical_significance":[]},{"alleles":["A","T"],"end":140470142,"feature_type":"variation","strand":1,"source":"dbSNP","start":140470142,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs144592133","seq_region_name":"7"},{"seq_region_name":"7","id":"rs537314189","clinical_significance":[],"end":140470143,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140470143,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs966633822","seq_region_name":"7","clinical_significance":[],"start":140470144,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140470144,"alleles":["G","A","C"],"strand":1,"feature_type":"variation"},{"alleles":["C","T"],"end":140470145,"feature_type":"variation","strand":1,"source":"dbSNP","start":140470145,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs916813479","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs947763025","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470146,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140470146},{"seq_region_name":"7","id":"rs1466196745","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140470147,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470147,"source":"dbSNP"},{"source":"dbSNP","start":140470149,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C","T"],"end":140470149,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1406687561"},{"start":140470151,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140470151,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130333266","clinical_significance":[]},{"start":140470152,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140470152,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794883713","clinical_significance":[]},{"end":140470155,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140470155,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794883781","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470157,"feature_type":"variation","strand":1,"end":140470157,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1321043342"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1348832037","source":"dbSNP","start":140470158,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C","G"],"end":140470158,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794883972","alleles":["G","A"],"end":140470160,"feature_type":"variation","strand":1,"source":"dbSNP","start":140470160,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs13229884","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470164,"feature_type":"variation","strand":1,"end":140470164,"alleles":["T","A","C","G"]},{"end":140470165,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140470165,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1029692998","seq_region_name":"7"},{"source":"dbSNP","start":140470168,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140470168,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1190026713"},{"end":140470169,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140470169,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794884304"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1348553327","source":"dbSNP","start":140470172,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140470172,"alleles":["G","A"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140470174,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470174,"source":"dbSNP","id":"rs1585488490","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1443240082","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470175,"source":"dbSNP","strand":1,"feature_type":"variation","end":140470175,"alleles":["C","T"]},{"id":"rs1794884556","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470177,"source":"dbSNP","strand":1,"feature_type":"variation","end":140470177,"alleles":["T","A"]},{"seq_region_name":"7","id":"rs1227571167","clinical_significance":[],"alleles":["G","A"],"end":140470178,"strand":1,"feature_type":"variation","start":140470178,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1794884702","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470180,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140470180},{"seq_region_name":"7","id":"rs1794884770","clinical_significance":[],"alleles":["T","C"],"end":140470182,"strand":1,"feature_type":"variation","start":140470182,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs192543869","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470185,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140470185},{"seq_region_name":"7","id":"rs1199752469","clinical_significance":[],"end":140470187,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140470187,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["T","G"],"end":140470188,"strand":1,"feature_type":"variation","start":140470188,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794884945","clinical_significance":[]},{"end":140470189,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140470189,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794885003"},{"seq_region_name":"7","id":"rs1794885064","clinical_significance":[],"start":140470192,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140470192,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1794885115","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470193,"source":"dbSNP","strand":1,"feature_type":"variation","end":140470193,"alleles":["C","G"]},{"alleles":["T","C","G"],"end":140470199,"feature_type":"variation","strand":1,"source":"dbSNP","start":140470199,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1293630073"},{"id":"rs2130333590","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140470200,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470200,"source":"dbSNP"},{"end":140470202,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140470202,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1794885259","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130333618","clinical_significance":[],"alleles":["C","G"],"end":140470203,"strand":1,"feature_type":"variation","start":140470203,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1459481998","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140470206,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470206,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794885359","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140470207,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470207},{"alleles":["A","C","G"],"end":140470209,"strand":1,"feature_type":"variation","start":140470209,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1274449454","clinical_significance":[]},{"id":"rs1193594843","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470211,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140470211},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794885521","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470213,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140470213},{"alleles":["CC","CCC"],"end":140470214,"strand":1,"feature_type":"variation","start":140470213,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794885578","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470214,"source":"dbSNP","strand":1,"feature_type":"variation","end":140470214,"alleles":["C","T"],"seq_region_name":"7","id":"rs1794885634","clinical_significance":[]},{"seq_region_name":"7","id":"rs115738944","clinical_significance":[],"strand":1,"feature_type":"variation","end":140470215,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470215,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1284464157","clinical_significance":[],"end":140470217,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140470217,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140470218,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140470218,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130333759","clinical_significance":[]},{"id":"rs1247897632","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140470220,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470220,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130333785","end":140470220,"alleles":["G","GG"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140470220,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140470221,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470221,"clinical_significance":[],"seq_region_name":"7","id":"rs1794885846"},{"start":140470221,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140470232,"alleles":["AAAAAAAAAAAA","AAAAAAAAAA","AAAAAAAAAAA","AAAAAAAAAAAAA","AAAAAAAAAAAAAA"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1277671425","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs75970201","end":140470222,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140470222,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130333861","source":"dbSNP","start":140470223,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140470223,"feature_type":"variation","strand":1},{"id":"rs1794886104","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140470225,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470225,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470228,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140470228,"seq_region_name":"7","id":"rs1447339671","clinical_significance":[]},{"seq_region_name":"7","id":"rs1211900582","clinical_significance":[],"start":140470232,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140470232,"strand":1,"feature_type":"variation"},{"alleles":["G","A"],"end":140470233,"feature_type":"variation","strand":1,"source":"dbSNP","start":140470233,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1337503284"},{"source":"dbSNP","start":140470239,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140470239,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1585488596","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470240,"feature_type":"variation","strand":1,"end":140470240,"alleles":["T","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1287967824"},{"clinical_significance":[],"id":"rs1451169993","seq_region_name":"7","alleles":["T","G"],"end":140470243,"feature_type":"variation","strand":1,"source":"dbSNP","start":140470243,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794886576","source":"dbSNP","start":140470247,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140470254,"alleles":["AAACCAAA","AAACCAAAACCAAA"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140470252,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140470254,"alleles":["AAA","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1326886327"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1205955392","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470260,"feature_type":"variation","strand":1,"end":140470260,"alleles":["C","A"]},{"alleles":["T","C"],"end":140470261,"strand":1,"feature_type":"variation","start":140470261,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs940428328","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794886861","alleles":["C","T"],"end":140470263,"feature_type":"variation","strand":1,"source":"dbSNP","start":140470263,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["ACA","A"],"end":140470268,"feature_type":"variation","strand":1,"source":"dbSNP","start":140470266,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1409508872","seq_region_name":"7"},{"id":"rs1794886985","seq_region_name":"7","clinical_significance":[],"start":140470267,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140470267,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"alleles":["C","T"],"end":140470271,"feature_type":"variation","strand":1,"source":"dbSNP","start":140470271,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794887039"},{"start":140470272,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140470272,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794887102","clinical_significance":[]},{"id":"rs184351524","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140470273,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470273,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140470274,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470274,"source":"dbSNP","id":"rs1471861297","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1181930244","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470276,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140470276},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794887340","source":"dbSNP","start":140470277,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140470277,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470278,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140470278,"clinical_significance":[],"id":"rs1422986720","seq_region_name":"7"},{"alleles":["T","G"],"end":140470279,"strand":1,"feature_type":"variation","start":140470279,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794887458","clinical_significance":[]},{"start":140470280,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140470280,"strand":1,"feature_type":"variation","id":"rs1794887525","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1369368885","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140470281,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470281,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140470283,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470283,"clinical_significance":[],"id":"rs1794887656","seq_region_name":"7"},{"alleles":["C","G"],"end":140470284,"strand":1,"feature_type":"variation","start":140470284,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1794887708","seq_region_name":"7","clinical_significance":[]},{"id":"rs1384923826","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140470285,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470285,"source":"dbSNP"},{"source":"dbSNP","start":140470289,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140470289,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794887816"},{"id":"rs1179687076","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470295,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","-"],"end":140470295},{"alleles":["C","T"],"end":140470295,"strand":1,"feature_type":"variation","start":140470295,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1471414273","clinical_significance":[]},{"source":"dbSNP","start":140470301,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140470301,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1473959621"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470303,"source":"dbSNP","strand":1,"feature_type":"variation","end":140470303,"alleles":["G","T"],"seq_region_name":"7","id":"rs1231721933","clinical_significance":[]},{"id":"rs1161145366","seq_region_name":"7","clinical_significance":[],"alleles":["C","A","T"],"end":140470310,"strand":1,"feature_type":"variation","start":140470310,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1036617435","alleles":["C","G","T"],"end":140470312,"feature_type":"variation","strand":1,"source":"dbSNP","start":140470312,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1256164474","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470313,"feature_type":"variation","strand":1,"end":140470313,"alleles":["C","T"]},{"strand":1,"feature_type":"variation","end":140470315,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470315,"source":"dbSNP","id":"rs756997991","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794888349","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470320,"source":"dbSNP","strand":1,"feature_type":"variation","end":140470320,"alleles":["C","A"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470322,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140470322,"seq_region_name":"7","id":"rs1224183578","clinical_significance":[]},{"clinical_significance":[],"id":"rs1794888477","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140470323,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470323},{"alleles":["G","A","C"],"end":140470327,"feature_type":"variation","strand":1,"source":"dbSNP","start":140470327,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1585488734","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140470328,"alleles":["T","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470328,"source":"dbSNP","seq_region_name":"7","id":"rs1585488744","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1429909883","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140470331,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470331},{"clinical_significance":[],"seq_region_name":"7","id":"rs375959231","feature_type":"variation","strand":1,"alleles":["C","A","G"],"end":140470332,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470332},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470336,"feature_type":"variation","strand":1,"end":140470336,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs55714045"},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140470337,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470337,"clinical_significance":[],"seq_region_name":"7","id":"rs1794888903"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130334663","source":"dbSNP","start":140470338,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["-","TACTCCGGAAGATGAGGCAGGAGAATCGCTTGA"],"end":140470337,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794888970","end":140470341,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140470341,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1240632447","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140470347,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470347},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470350,"feature_type":"variation","strand":1,"end":140470350,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs933120027"},{"alleles":["G","A"],"end":140470351,"feature_type":"variation","strand":1,"source":"dbSNP","start":140470351,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1050370651"},{"end":140470354,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140470354,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130334736"},{"end":140470355,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140470355,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs538618976","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs187136926","source":"dbSNP","start":140470356,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140470356,"alleles":["G","A","T"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470357,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140470357,"seq_region_name":"7","id":"rs755833287","clinical_significance":[]},{"alleles":["G","A"],"end":140470358,"strand":1,"feature_type":"variation","start":140470358,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1342091677","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["GTGGATCACCTGAGGTCAG","G"],"end":140470376,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470358,"source":"dbSNP","id":"rs1794889509","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs779783560","clinical_significance":[],"strand":1,"feature_type":"variation","end":140470361,"alleles":["GG","GGG"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470360,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1242318860","seq_region_name":"7","end":140470362,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140470362,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs532870826","clinical_significance":[],"end":140470366,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140470366,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["T","A"],"end":140470368,"feature_type":"variation","strand":1,"source":"dbSNP","start":140470368,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1794889809","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1794889860","clinical_significance":[],"end":140470373,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140470373,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140470374,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140470374,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1282707234","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470374,"feature_type":"variation","strand":1,"end":140470375,"alleles":["CA","-"],"clinical_significance":[],"id":"rs1794889976","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs912969687","alleles":["A","C"],"end":140470375,"feature_type":"variation","strand":1,"source":"dbSNP","start":140470375,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140470377,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140470377,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585488864"},{"seq_region_name":"7","id":"rs1406417488","clinical_significance":[],"end":140470378,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140470378,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470380,"feature_type":"variation","strand":1,"end":140470380,"alleles":["T","C"],"clinical_significance":[],"id":"rs1358906845","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140470381,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470381,"source":"dbSNP","seq_region_name":"7","id":"rs1794890261","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs999589341","source":"dbSNP","start":140470382,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140470382,"alleles":["C","T"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470383,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140470383,"clinical_significance":[],"seq_region_name":"7","id":"rs1031492244"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470386,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140470386,"seq_region_name":"7","id":"rs1585488910","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1276809093","source":"dbSNP","start":140470387,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140470387,"alleles":["C","G"],"feature_type":"variation","strand":1},{"id":"rs1482380832","seq_region_name":"7","clinical_significance":[],"start":140470388,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140470388,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1489694495","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470394,"source":"dbSNP","strand":1,"feature_type":"variation","end":140470394,"alleles":["G","C"]},{"end":140470401,"alleles":["CAACA","CA"],"strand":1,"feature_type":"variation","start":140470397,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1267798949","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470398,"source":"dbSNP","strand":1,"feature_type":"variation","end":140470398,"alleles":["A","T"],"seq_region_name":"7","id":"rs1794890700","clinical_significance":[]},{"seq_region_name":"7","id":"rs1217032872","clinical_significance":[],"alleles":["C","A","T"],"end":140470400,"strand":1,"feature_type":"variation","start":140470400,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140470402,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470402,"source":"dbSNP","seq_region_name":"7","id":"rs1794890912","clinical_significance":[]},{"end":140470404,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140470404,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1205129672","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140470406,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140470406,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794891125"},{"seq_region_name":"7","id":"rs1794891188","clinical_significance":[],"end":140470408,"alleles":["-","TTTTT"],"strand":1,"feature_type":"variation","start":140470409,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1794891244","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470410,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CTCC","-"],"end":140470413},{"feature_type":"variation","strand":1,"end":140470418,"alleles":["CTCCGTCTC","CTC"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470410,"clinical_significance":[],"seq_region_name":"7","id":"rs1794891297"},{"source":"dbSNP","start":140470411,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140470411,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1257455815"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470413,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140470413,"seq_region_name":"7","id":"rs1444553852","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140470414,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470414,"clinical_significance":[],"seq_region_name":"7","id":"rs1345665892"},{"id":"rs1794891545","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140470415,"strand":1,"feature_type":"variation","start":140470415,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1185864220","clinical_significance":[],"start":140470419,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140470419,"strand":1,"feature_type":"variation"},{"end":140470420,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140470420,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1236539767"},{"end":140470421,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140470421,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs949959116"},{"clinical_significance":[],"id":"rs1449648672","seq_region_name":"7","source":"dbSNP","start":140470422,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140470422,"alleles":["T","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1345085476","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470427,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140470427},{"clinical_significance":[],"seq_region_name":"7","id":"rs563885230","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140470428,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470428},{"clinical_significance":[],"seq_region_name":"7","id":"rs572122826","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470430,"feature_type":"variation","strand":1,"end":140470430,"alleles":["C","A","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1013705148","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140470438,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470438},{"seq_region_name":"7","id":"rs1343745681","clinical_significance":[],"start":140470440,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","-"],"end":140470440,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs202121634","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140470441,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470441,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794892261","end":140470456,"alleles":["GGTGTGGTGGCGGG","GG"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140470443,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140470444,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140470444,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1023850131"},{"id":"rs2130335515","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470447,"source":"dbSNP","strand":1,"feature_type":"variation","end":140470447,"alleles":["T","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794892377","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470448,"feature_type":"variation","strand":1,"end":140470448,"alleles":["G","A","C"]},{"seq_region_name":"7","id":"rs1794892454","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470449,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140470449},{"end":140470453,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140470453,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1415508359","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470454,"source":"dbSNP","strand":1,"feature_type":"variation","end":140470454,"alleles":["G","A"],"seq_region_name":"7","id":"rs1173145360","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130335593","clinical_significance":[],"start":140470456,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["-","T"],"end":140470455,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470456,"source":"dbSNP","strand":1,"feature_type":"variation","end":140470456,"alleles":["G","A"],"seq_region_name":"7","id":"rs969573345","clinical_significance":[]},{"clinical_significance":[],"id":"rs1404256937","seq_region_name":"7","alleles":["C","T"],"end":140470457,"feature_type":"variation","strand":1,"source":"dbSNP","start":140470457,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140470458,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140470457,"alleles":["-","AT"],"strand":1,"feature_type":"variation","id":"rs2130335638","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794892762","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470458,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140470458},{"clinical_significance":[],"seq_region_name":"7","id":"rs984881410","end":140470463,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140470463,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140470464,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AATC","AATCAATC"],"end":140470467,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs537310796"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470467,"source":"dbSNP","strand":1,"feature_type":"variation","end":140470467,"alleles":["C","G","T"],"id":"rs908847696","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1186806436","source":"dbSNP","start":140470468,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140470468,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470474,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140470474,"seq_region_name":"7","id":"rs1794893118","clinical_significance":[]},{"source":"dbSNP","start":140470477,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140470477,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs961999706"},{"start":140470478,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140470478,"alleles":["C","A","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs971861615","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470479,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140470479,"seq_region_name":"7","id":"rs923011427","clinical_significance":[]},{"start":140470481,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140470481,"alleles":["A","C"],"strand":1,"feature_type":"variation","id":"rs1461694640","seq_region_name":"7","clinical_significance":[]},{"start":140470482,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140470482,"alleles":["A","G"],"strand":1,"feature_type":"variation","id":"rs1264972161","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs531359850","clinical_significance":[],"alleles":["T","A"],"end":140470485,"strand":1,"feature_type":"variation","start":140470485,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140470488,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470488,"clinical_significance":[],"seq_region_name":"7","id":"rs1050221789"},{"alleles":["A","AA"],"end":140470491,"strand":1,"feature_type":"variation","start":140470491,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1436041901","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1322991882","end":140470492,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140470492,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1794893756","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","T"],"end":140470494,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470494},{"seq_region_name":"7","id":"rs549786776","clinical_significance":[],"start":140470496,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140470496,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140470498,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140470498,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794893872"},{"id":"rs910475908","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","G","T"],"end":140470499,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470499,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140470500,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470500,"clinical_significance":[],"seq_region_name":"7","id":"rs1360174160"},{"seq_region_name":"7","id":"rs1585489142","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140470503,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470503,"source":"dbSNP"},{"end":140470507,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140470507,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs887754751","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794894280","clinical_significance":[],"start":140470509,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140470509,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140470510,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140470510,"alleles":["A","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1340195274","seq_region_name":"7"},{"end":140470511,"alleles":["AG","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140470510,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs555760296"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794894467","source":"dbSNP","start":140470511,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140470511,"alleles":["G","A"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140470516,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470516,"clinical_significance":[],"seq_region_name":"7","id":"rs1794894527"},{"end":140470517,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140470517,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs191907234"},{"id":"rs866592803","seq_region_name":"7","clinical_significance":[],"end":140470520,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140470520,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140470521,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140470521,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1794894660","seq_region_name":"7"},{"end":140470522,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140470522,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585489182"},{"seq_region_name":"7","id":"rs1257167318","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470523,"source":"dbSNP","strand":1,"feature_type":"variation","end":140470523,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs2130336212","clinical_significance":[],"strand":1,"feature_type":"variation","end":140470525,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470525,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1429871167","source":"dbSNP","start":140470527,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140470527,"alleles":["G","A","T"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470528,"feature_type":"variation","strand":1,"end":140470528,"alleles":["T","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs901919309"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1347674470","source":"dbSNP","start":140470533,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140470533,"feature_type":"variation","strand":1},{"alleles":["G","A"],"end":140470534,"strand":1,"feature_type":"variation","start":140470534,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs529044547","clinical_significance":[]},{"end":140470536,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140470536,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585489218"},{"seq_region_name":"7","id":"rs903883784","clinical_significance":[],"end":140470538,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140470538,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470539,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140470539,"seq_region_name":"7","id":"rs1460820677","clinical_significance":[]},{"id":"rs2130336349","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470539,"source":"dbSNP","strand":1,"feature_type":"variation","end":140470540,"alleles":["TG","-"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1278311504","alleles":["C","T"],"end":140470541,"feature_type":"variation","strand":1,"source":"dbSNP","start":140470541,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs2130336381","clinical_significance":[],"alleles":["-","TT"],"end":140470541,"strand":1,"feature_type":"variation","start":140470542,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1465604348","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140470542,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470542},{"strand":1,"feature_type":"variation","end":140470547,"alleles":["T","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470547,"source":"dbSNP","seq_region_name":"7","id":"rs1794895300","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794895356","source":"dbSNP","start":140470548,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140470548,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1190161401","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140470549,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470549,"source":"dbSNP"},{"start":140470549,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140470551,"alleles":["CAC","CACAC"],"strand":1,"feature_type":"variation","id":"rs1305964217","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470550,"source":"dbSNP","strand":1,"feature_type":"variation","end":140470550,"alleles":["A","G"],"seq_region_name":"7","id":"rs1794895547","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140470552,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470552,"clinical_significance":[],"seq_region_name":"7","id":"rs1272618262"},{"feature_type":"variation","strand":1,"end":140470554,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470554,"clinical_significance":[],"seq_region_name":"7","id":"rs1245801317"},{"end":140470556,"alleles":["AG","AGAG"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140470555,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794895654"},{"seq_region_name":"7","id":"rs1229248661","clinical_significance":[],"alleles":["CC","C"],"end":140470558,"strand":1,"feature_type":"variation","start":140470557,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794895748","source":"dbSNP","start":140470559,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140470559,"alleles":["T","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs999916365","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470563,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140470563},{"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140470564,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470564,"source":"dbSNP","seq_region_name":"7","id":"rs1052508552","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794895929","feature_type":"variation","strand":1,"end":140470567,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470567},{"start":140470569,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140470569,"alleles":["G","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1452493317","clinical_significance":[]},{"id":"rs1794896023","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140470571,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470571,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470572,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140470572,"clinical_significance":[],"seq_region_name":"7","id":"rs547239052"},{"source":"dbSNP","start":140470575,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140470575,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1379308990"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470577,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140470577,"seq_region_name":"7","id":"rs1378316660","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470586,"feature_type":"variation","strand":1,"end":140470586,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1013708788"},{"seq_region_name":"7","id":"rs1298225572","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470586,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AAACAAAACAAA","AAACAAA"],"end":140470597},{"source":"dbSNP","start":140470589,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140470589,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794896357"},{"feature_type":"variation","strand":1,"end":140470591,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470591,"clinical_significance":[],"seq_region_name":"7","id":"rs1463105075"},{"feature_type":"variation","strand":1,"end":140470601,"alleles":["AAACAAACAAA","AAACAAA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470591,"clinical_significance":[],"seq_region_name":"7","id":"rs1794896451"},{"clinical_significance":[],"id":"rs1794896513","seq_region_name":"7","feature_type":"variation","strand":1,"end":140470626,"alleles":["AAACAAACAAAAAAACCCAAACAAACAAACAAAAAA","AAACAAACAAAAAA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470591},{"seq_region_name":"7","id":"rs62490448","clinical_significance":[],"end":140470593,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","start":140470593,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs28784908","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470595,"source":"dbSNP","strand":1,"feature_type":"variation","end":140470595,"alleles":["A","C"]},{"start":140470599,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140470599,"alleles":["A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1389162995","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1169377337","end":140470605,"alleles":["AAAAAAA","AAAAAA","AAAAAAAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140470599,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs539509531","clinical_significance":[],"alleles":["A","G"],"end":140470604,"strand":1,"feature_type":"variation","start":140470604,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140470606,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470606,"source":"dbSNP","seq_region_name":"7","id":"rs1386791644","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470608,"source":"dbSNP","strand":1,"feature_type":"variation","end":140470623,"alleles":["CAAACAAACAAACAAA","CAAACAAACAAA","CAAACAAACAAACAAACAAA"],"id":"rs547480688","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","C"],"end":140470609,"feature_type":"variation","strand":1,"source":"dbSNP","start":140470609,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1001042545","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1178997451","source":"dbSNP","start":140470614,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140470614,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1322874547","clinical_significance":[],"start":140470617,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140470617,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1794897184","clinical_significance":[],"alleles":["A","G"],"end":140470619,"strand":1,"feature_type":"variation","start":140470619,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794897238","end":140470620,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140470620,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140470621,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140470626,"alleles":["AAAAAA","AAA"],"strand":1,"feature_type":"variation","id":"rs1794897288","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140470624,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470624,"source":"dbSNP","seq_region_name":"7","id":"rs2130336991","clinical_significance":[]},{"seq_region_name":"7","id":"rs1223435444","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140470625,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470625,"source":"dbSNP"},{"source":"dbSNP","start":140470625,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AACAA","AA"],"end":140470629,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1032656003"},{"clinical_significance":[],"id":"rs1585489427","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470627,"feature_type":"variation","strand":1,"end":140470627,"alleles":["C","A"]},{"seq_region_name":"7","id":"rs1361898667","clinical_significance":[],"end":140470628,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140470628,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470631,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140470631,"seq_region_name":"7","id":"rs28880113","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140470632,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470632,"clinical_significance":[],"seq_region_name":"7","id":"rs1006500891"},{"alleles":["G","C"],"end":140470634,"feature_type":"variation","strand":1,"source":"dbSNP","start":140470634,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs913014045"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1374703637","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470635,"feature_type":"variation","strand":1,"end":140470635,"alleles":["G","A","T"]},{"seq_region_name":"7","id":"rs1794897829","clinical_significance":[],"start":140470636,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140470641,"alleles":["CTGGGC","-"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470638,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140470638,"seq_region_name":"7","id":"rs369847440","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470644,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140470644,"clinical_significance":[],"seq_region_name":"7","id":"rs1309868501"},{"alleles":["T","C"],"end":140470646,"feature_type":"variation","strand":1,"source":"dbSNP","start":140470646,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1016909004"},{"alleles":["G","A"],"end":140470647,"strand":1,"feature_type":"variation","start":140470647,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1392613259","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs569920789","source":"dbSNP","start":140470651,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140470651,"alleles":["C","T"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140470652,"alleles":["A","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470652,"clinical_significance":[],"seq_region_name":"7","id":"rs1381728404"},{"seq_region_name":"7","id":"rs1794898190","clinical_significance":[],"end":140470655,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140470655,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs2130337244","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140470656,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470656,"source":"dbSNP"},{"id":"rs1794898228","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470657,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140470657},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585489517","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470658,"feature_type":"variation","strand":1,"end":140470658,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794898335","end":140470659,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140470659,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["A","C","T"],"end":140470660,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470660,"clinical_significance":[],"seq_region_name":"7","id":"rs961774874"},{"seq_region_name":"7","id":"rs113609274","clinical_significance":[],"end":140470664,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140470664,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140470666,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140470666,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1224913471"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1333363908","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470670,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140470670},{"start":140470673,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140470673,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs923026323","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140470675,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470675,"clinical_significance":[],"id":"rs954408334","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470678,"feature_type":"variation","strand":1,"end":140470678,"alleles":["G","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794898772"},{"seq_region_name":"7","id":"rs985982384","clinical_significance":[],"start":140470681,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G","T"],"end":140470681,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs937260477","feature_type":"variation","strand":1,"end":140470682,"alleles":["G","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470682},{"start":140470685,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140470685,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs1417256240","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470690,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140470690,"clinical_significance":[],"seq_region_name":"7","id":"rs1249826340"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1200255182","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470698,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140470698},{"clinical_significance":[],"id":"rs772211196","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140470700,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470700},{"id":"rs1563094744","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470704,"source":"dbSNP","strand":1,"feature_type":"variation","end":140470704,"alleles":["T","C"]},{"start":140470709,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140470709,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1263036654","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140470713,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470713,"source":"dbSNP","seq_region_name":"7","id":"rs866932281","clinical_significance":[]},{"clinical_significance":[],"id":"rs1262877699","seq_region_name":"7","source":"dbSNP","start":140470714,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140470714,"feature_type":"variation","strand":1},{"end":140470718,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140470718,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs775724728","clinical_significance":[]},{"seq_region_name":"7","id":"rs1237430708","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470719,"source":"dbSNP","strand":1,"feature_type":"variation","end":140470719,"alleles":["T","TT"]},{"seq_region_name":"7","id":"rs1794899201","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140470724,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470724,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470725,"feature_type":"variation","strand":1,"end":140470725,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1330315332"},{"end":140470726,"alleles":["G","C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140470726,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1316876836"},{"alleles":["C","T"],"end":140470728,"feature_type":"variation","strand":1,"source":"dbSNP","start":140470728,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1287109026"},{"id":"rs947197640","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140470731,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470731,"source":"dbSNP"},{"alleles":["A","C","G","T"],"end":140470732,"strand":1,"feature_type":"variation","start":140470732,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs978726616","seq_region_name":"7","clinical_significance":[]},{"start":140470732,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["ATGATGA","ATGA"],"end":140470738,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794899632","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1300704252","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470736,"feature_type":"variation","strand":1,"end":140470736,"alleles":["T","C","G"]},{"id":"rs1794899852","seq_region_name":"7","clinical_significance":[],"start":140470737,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140470737,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1794899909","clinical_significance":[],"start":140470741,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["CCC","CC"],"end":140470743,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794899966","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140470742,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470742},{"clinical_significance":[],"seq_region_name":"7","id":"rs1265851224","feature_type":"variation","strand":1,"alleles":["CT","-"],"end":140470744,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470743},{"id":"rs1794900100","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140470744,"strand":1,"feature_type":"variation","start":140470744,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1036362592","source":"dbSNP","start":140470745,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","GG"],"end":140470745,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140470745,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140470745,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794900157"},{"feature_type":"variation","strand":1,"end":140470759,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470759,"clinical_significance":[],"id":"rs924521502","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470762,"feature_type":"variation","strand":1,"end":140470762,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794900365"},{"seq_region_name":"7","id":"rs1794900425","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140470767,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470767,"source":"dbSNP"},{"source":"dbSNP","start":140470773,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140470773,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs373987127","seq_region_name":"7"},{"end":140470774,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140470774,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs62490449"},{"clinical_significance":[],"seq_region_name":"7","id":"rs771235509","alleles":["G","A"],"end":140470776,"feature_type":"variation","strand":1,"source":"dbSNP","start":140470776,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1363203686","clinical_significance":[],"alleles":["T","C","G"],"end":140470779,"strand":1,"feature_type":"variation","start":140470779,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1177199582","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470781,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140470781},{"seq_region_name":"7","id":"rs949441668","clinical_significance":[],"alleles":["C","T"],"end":140470787,"strand":1,"feature_type":"variation","start":140470787,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470788,"source":"dbSNP","strand":1,"feature_type":"variation","end":140470788,"alleles":["G","A"],"seq_region_name":"7","id":"rs769647114","clinical_significance":[]},{"seq_region_name":"7","id":"rs1198899350","clinical_significance":[],"alleles":["A","C"],"end":140470792,"strand":1,"feature_type":"variation","start":140470792,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140470794,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470794,"clinical_significance":[],"seq_region_name":"7","id":"rs1585489710"},{"alleles":["A","G"],"end":140470797,"strand":1,"feature_type":"variation","start":140470797,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794901034","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794901085","source":"dbSNP","start":140470800,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140470800,"alleles":["C","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794901134","feature_type":"variation","strand":1,"end":140470801,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470801},{"id":"rs1430922456","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470802,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140470802},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130337962","end":140470803,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140470803,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1794901248","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140470807,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470807,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1198140589","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470809,"feature_type":"variation","strand":1,"end":140470809,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs2130337992","clinical_significance":[],"alleles":["G","C"],"end":140470810,"strand":1,"feature_type":"variation","start":140470810,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140470814,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470814,"source":"dbSNP","seq_region_name":"7","id":"rs1794901346","clinical_significance":[]},{"end":140470815,"alleles":["A","G","T"],"strand":1,"feature_type":"variation","start":140470815,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs2130338013","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140470816,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470816,"source":"dbSNP","seq_region_name":"7","id":"rs2130338034","clinical_significance":[]},{"id":"rs889265710","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470817,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140470817},{"clinical_significance":[],"id":"rs1051043822","seq_region_name":"7","source":"dbSNP","start":140470817,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140470818,"alleles":["TG","-"],"feature_type":"variation","strand":1},{"alleles":["A","G"],"end":140470819,"feature_type":"variation","strand":1,"source":"dbSNP","start":140470819,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794901514"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1473490061","source":"dbSNP","start":140470821,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140470821,"alleles":["G","T"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140470823,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AGGAG","AG"],"end":140470827,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794901649"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140470824,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470824,"source":"dbSNP","seq_region_name":"7","id":"rs1203780452","clinical_significance":[]},{"clinical_significance":[],"id":"rs565179546","seq_region_name":"7","source":"dbSNP","start":140470825,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140470825,"alleles":["G","A"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470827,"feature_type":"variation","strand":1,"end":140470827,"alleles":["G","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs905382449"},{"source":"dbSNP","start":140470829,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140470829,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1000968984"},{"id":"rs1203748520","seq_region_name":"7","clinical_significance":[],"start":140470830,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140470830,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1453263299","clinical_significance":[],"alleles":["T","C"],"end":140470831,"strand":1,"feature_type":"variation","start":140470831,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140470833,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140470833,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1006796854"},{"end":140470835,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140470835,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794902206","clinical_significance":[]},{"clinical_significance":[],"id":"rs1032592425","seq_region_name":"7","end":140470838,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140470838,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140470839,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470839,"source":"dbSNP","seq_region_name":"7","id":"rs1294308922","clinical_significance":[]},{"seq_region_name":"7","id":"rs1393031693","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470841,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140470841},{"alleles":["G","A"],"end":140470842,"strand":1,"feature_type":"variation","start":140470842,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1385141248","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs555766215","clinical_significance":[],"strand":1,"feature_type":"variation","end":140470847,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470847,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140470849,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470849,"source":"dbSNP","seq_region_name":"7","id":"rs1351567136","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["-","TG"],"end":140470849,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470850,"clinical_significance":[],"seq_region_name":"7","id":"rs1794902661"},{"source":"dbSNP","start":140470850,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140470850,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794902713"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470852,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140470852,"seq_region_name":"7","id":"rs1794902766","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794902815","feature_type":"variation","strand":1,"end":140470856,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470856},{"seq_region_name":"7","id":"rs1380352325","clinical_significance":[],"start":140470858,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140470858,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs956952274","clinical_significance":[],"start":140470860,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C","G"],"end":140470860,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470864,"feature_type":"variation","strand":1,"end":140470864,"alleles":["C","G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794902974"},{"feature_type":"variation","strand":1,"end":140470865,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470865,"clinical_significance":[],"seq_region_name":"7","id":"rs574424037"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794903129","source":"dbSNP","start":140470866,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140470866,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1470923372","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470866,"feature_type":"variation","strand":1,"alleles":["GAGA","GA"],"end":140470869},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470867,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140470867,"clinical_significance":[],"id":"rs1286790680","seq_region_name":"7"},{"alleles":["G","A"],"end":140470868,"feature_type":"variation","strand":1,"source":"dbSNP","start":140470868,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1315995799","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1245123134","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470870,"source":"dbSNP","strand":1,"feature_type":"variation","end":140470872,"alleles":["TCT","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585489885","end":140470872,"alleles":["T","A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140470872,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140470878,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470878,"source":"dbSNP","seq_region_name":"7","id":"rs773239169","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1475837340","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140470880,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470880},{"clinical_significance":[],"seq_region_name":"7","id":"rs1375052092","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470884,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140470884},{"seq_region_name":"7","id":"rs1487254248","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470884,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","TT"],"end":140470884},{"end":140470886,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140470886,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794903819"},{"source":"dbSNP","start":140470891,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C","G"],"end":140470891,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1019914865"},{"seq_region_name":"7","id":"rs1794903942","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["GGG","GG"],"end":140470894,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470892,"source":"dbSNP"},{"source":"dbSNP","start":140470895,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140470895,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs371392949"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1428364457","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470896,"feature_type":"variation","strand":1,"alleles":["AA","A"],"end":140470897},{"source":"dbSNP","start":140470898,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140470898,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794904111"},{"start":140470899,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C","G"],"end":140470899,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794904170","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140470900,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470900,"source":"dbSNP","seq_region_name":"7","id":"rs1221090926","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470901,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140470901,"clinical_significance":[],"seq_region_name":"7","id":"rs535227442"},{"seq_region_name":"7","id":"rs1794904310","clinical_significance":[],"strand":1,"feature_type":"variation","end":140470902,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470902,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470903,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140470903,"id":"rs1483962927","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470904,"feature_type":"variation","strand":1,"end":140470904,"alleles":["G","A","T"],"clinical_significance":[],"id":"rs1460379188","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585489969","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470908,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140470908},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140470909,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470909,"source":"dbSNP","id":"rs1794904545","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140470913,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470913,"source":"dbSNP","seq_region_name":"7","id":"rs898035604","clinical_significance":[]},{"end":140470914,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140470914,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs762630851","clinical_significance":[]},{"id":"rs1339618094","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140470917,"strand":1,"feature_type":"variation","start":140470917,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["C","T"],"end":140470919,"feature_type":"variation","strand":1,"source":"dbSNP","start":140470919,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs958555785"},{"clinical_significance":[],"seq_region_name":"7","id":"rs927018560","alleles":["CACACACACA","CACACA","CACACACA"],"end":140470928,"feature_type":"variation","strand":1,"source":"dbSNP","start":140470919,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["A","T"],"end":140470920,"feature_type":"variation","strand":1,"source":"dbSNP","start":140470920,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794904972"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470922,"source":"dbSNP","strand":1,"feature_type":"variation","end":140470922,"alleles":["A","G"],"seq_region_name":"7","id":"rs1364118378","clinical_significance":[]},{"seq_region_name":"7","id":"rs766222725","clinical_significance":[],"start":140470925,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140470925,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794905190","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470927,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140470927},{"start":140470928,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140470928,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs984614184","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140470933,"alleles":["AAAAAA","AAAAAAAAAA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470928,"source":"dbSNP","seq_region_name":"7","id":"rs1794905303","clinical_significance":[]},{"seq_region_name":"7","id":"rs751211854","clinical_significance":[],"alleles":["A","C"],"end":140470929,"strand":1,"feature_type":"variation","start":140470929,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140470934,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470934,"clinical_significance":[],"seq_region_name":"7","id":"rs1333566589"},{"seq_region_name":"7","id":"rs1411011092","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470941,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140470941},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794905467","end":140470942,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140470942,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470943,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140470943,"seq_region_name":"7","id":"rs2130339070","clinical_significance":[]},{"source":"dbSNP","start":140470944,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140470944,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1398904988","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140470947,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470947,"source":"dbSNP","seq_region_name":"7","id":"rs1794905587","clinical_significance":[]},{"start":140470952,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140470952,"strand":1,"feature_type":"variation","id":"rs1166432239","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140470959,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140470959,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1794905699","seq_region_name":"7"},{"end":140470961,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140470961,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1429365799"},{"feature_type":"variation","strand":1,"end":140470962,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470962,"clinical_significance":[],"id":"rs909168419","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140470966,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470966,"clinical_significance":[],"seq_region_name":"7","id":"rs1794905851"},{"id":"rs115293713","seq_region_name":"7","clinical_significance":[],"start":140470972,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140470972,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140470973,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470973,"source":"dbSNP","id":"rs1794906217","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1443274336","source":"dbSNP","start":140470978,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140470978,"alleles":["T","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1243108532","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140470980,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470980,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794906470","feature_type":"variation","strand":1,"end":140470982,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140470982},{"strand":1,"feature_type":"variation","end":140470984,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470984,"source":"dbSNP","id":"rs1186213284","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","G"],"end":140470991,"feature_type":"variation","strand":1,"source":"dbSNP","start":140470991,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs766960735"},{"strand":1,"feature_type":"variation","alleles":["A","C","G","T"],"end":140470992,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470992,"source":"dbSNP","seq_region_name":"7","id":"rs28699169","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470992,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","-"],"end":140470992,"seq_region_name":"7","id":"rs1585490120","clinical_significance":[]},{"seq_region_name":"7","id":"rs1193648725","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140470993,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470993,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470994,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","T"],"end":140470994,"seq_region_name":"7","id":"rs1341059608","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1370410440","end":140470995,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140470995,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs28563126","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470997,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140470997},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140470998,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140470998,"seq_region_name":"7","id":"rs1357152229","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471000,"source":"dbSNP","strand":1,"feature_type":"variation","end":140471000,"alleles":["C","G","T"],"seq_region_name":"7","id":"rs778113540","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471006,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140471006,"id":"rs1443005752","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794907741","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471006,"feature_type":"variation","strand":1,"end":140471006,"alleles":["G","GG"]},{"clinical_significance":[],"id":"rs1337555475","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471008,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140471008},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471009,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AGAA","A"],"end":140471012,"seq_region_name":"7","id":"rs1326943343","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794907927","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471011,"feature_type":"variation","strand":1,"end":140471012,"alleles":["AA","-"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471012,"feature_type":"variation","strand":1,"end":140471012,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1050555246"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471013,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140471013,"seq_region_name":"7","id":"rs1366455926","clinical_significance":[]},{"id":"rs754419325","seq_region_name":"7","clinical_significance":[],"start":140471016,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A","C"],"end":140471016,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140471021,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471021,"source":"dbSNP","seq_region_name":"7","id":"rs1412172362","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794908413","clinical_significance":[],"end":140471027,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140471027,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140471034,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471034,"clinical_significance":[],"seq_region_name":"7","id":"rs1423202904"},{"id":"rs1306688847","seq_region_name":"7","clinical_significance":[],"start":140471040,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140471040,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"start":140471041,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140471041,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794908661","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794908743","clinical_significance":[],"end":140471042,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140471042,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["C","T"],"end":140471045,"feature_type":"variation","strand":1,"source":"dbSNP","start":140471045,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1159591824"},{"clinical_significance":[],"id":"rs1794908921","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140471048,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471048},{"feature_type":"variation","strand":1,"end":140471054,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471054,"clinical_significance":[],"seq_region_name":"7","id":"rs557864165"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1373123548","source":"dbSNP","start":140471058,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140471058,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1179077385","source":"dbSNP","start":140471064,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140471064,"alleles":["A","C"],"feature_type":"variation","strand":1},{"id":"rs1585490257","seq_region_name":"7","clinical_significance":[],"start":140471064,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140471066,"alleles":["AAA","A"],"strand":1,"feature_type":"variation"},{"start":140471066,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140471066,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794909382","clinical_significance":[]},{"id":"rs1794909491","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140471071,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471071,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471074,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140471074,"clinical_significance":[],"seq_region_name":"7","id":"rs1482510853"},{"seq_region_name":"7","id":"rs1224438309","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471082,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140471082},{"strand":1,"feature_type":"variation","end":140471083,"alleles":["CC","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471082,"source":"dbSNP","seq_region_name":"7","id":"rs1229236804","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471088,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140471088,"seq_region_name":"7","id":"rs1489815851","clinical_significance":[]},{"source":"dbSNP","start":140471092,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140471092,"alleles":["T","A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1001029639"},{"seq_region_name":"7","id":"rs1224208482","clinical_significance":[],"strand":1,"feature_type":"variation","end":140471093,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471093,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1794909918","seq_region_name":"7","end":140471095,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140471095,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471099,"source":"dbSNP","strand":1,"feature_type":"variation","end":140471099,"alleles":["T","C"],"seq_region_name":"7","id":"rs575933685","clinical_significance":[]},{"source":"dbSNP","start":140471100,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140471100,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs757690776","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471102,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140471102,"seq_region_name":"7","id":"rs1277806926","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140471103,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471103,"source":"dbSNP","seq_region_name":"7","id":"rs184468420","clinical_significance":[]},{"source":"dbSNP","start":140471106,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140471106,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1346379388"},{"end":140471115,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140471115,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794910280"},{"clinical_significance":[],"id":"rs934549540","seq_region_name":"7","source":"dbSNP","start":140471116,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140471116,"feature_type":"variation","strand":1},{"id":"rs375494370","seq_region_name":"7","clinical_significance":[],"start":140471117,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140471117,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1794910481","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471119,"source":"dbSNP","strand":1,"feature_type":"variation","end":140471119,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs917944273","feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140471120,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471120},{"seq_region_name":"7","id":"rs949368341","clinical_significance":[],"strand":1,"feature_type":"variation","end":140471122,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471122,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471125,"source":"dbSNP","strand":1,"feature_type":"variation","end":140471125,"alleles":["G","A"],"seq_region_name":"7","id":"rs1794910680","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs529108423","end":140471126,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140471126,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140471128,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471128,"source":"dbSNP","seq_region_name":"7","id":"rs1344268986","clinical_significance":[]},{"seq_region_name":"7","id":"rs540938633","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471129,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140471129},{"clinical_significance":[],"id":"rs2130340235","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140471130,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471130},{"strand":1,"feature_type":"variation","end":140471131,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471131,"source":"dbSNP","seq_region_name":"7","id":"rs1563094993","clinical_significance":[]},{"start":140471132,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140471132,"alleles":["C","A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1156277678","clinical_significance":[]},{"clinical_significance":[],"id":"rs1472017054","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471134,"feature_type":"variation","strand":1,"end":140471134,"alleles":["A","G"]},{"clinical_significance":[],"id":"rs2130340290","seq_region_name":"7","feature_type":"variation","strand":1,"end":140471135,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471135},{"start":140471142,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140471142,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794911161","clinical_significance":[]},{"id":"rs1429541475","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140471143,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471143,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1794911289","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140471144,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471144,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140471148,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471148,"source":"dbSNP","seq_region_name":"7","id":"rs1585490389","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471150,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140471150,"seq_region_name":"7","id":"rs1002940862","clinical_significance":[]},{"alleles":["A","C"],"end":140471151,"strand":1,"feature_type":"variation","start":140471151,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794911483","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794911541","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471152,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140471152},{"alleles":["C","T"],"end":140471154,"feature_type":"variation","strand":1,"source":"dbSNP","start":140471154,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs905265606"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471158,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140471158,"clinical_significance":[],"seq_region_name":"7","id":"rs2130340389"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471159,"feature_type":"variation","strand":1,"end":140471159,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130340406"},{"alleles":["T","C"],"end":140471162,"strand":1,"feature_type":"variation","start":140471162,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs559090450","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471166,"source":"dbSNP","strand":1,"feature_type":"variation","end":140471166,"alleles":["T","C"],"seq_region_name":"7","id":"rs2130340442","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1245876671","feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140471170,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471170},{"source":"dbSNP","start":140471172,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140471172,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794911787"},{"seq_region_name":"7","id":"rs1216268611","clinical_significance":[],"end":140471175,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140471175,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs779421929","clinical_significance":[],"end":140471179,"alleles":["T","C","G"],"strand":1,"feature_type":"variation","start":140471179,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140471180,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140471180,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130340508"},{"end":140471181,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140471181,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1208168710","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471184,"feature_type":"variation","strand":1,"end":140471184,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794912176"},{"start":140471187,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140471187,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794912262","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140471191,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471191,"clinical_significance":[],"seq_region_name":"7","id":"rs1324294375"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471192,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140471192,"clinical_significance":[],"seq_region_name":"7","id":"rs898098027"},{"strand":1,"feature_type":"variation","end":140471194,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471194,"source":"dbSNP","seq_region_name":"7","id":"rs746028532","clinical_significance":[]},{"end":140471195,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140471195,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1285273977","clinical_significance":[]},{"clinical_significance":[],"id":"rs993723538","seq_region_name":"7","end":140471196,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140471196,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140471201,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471201,"clinical_significance":[],"seq_region_name":"7","id":"rs2130340610"},{"seq_region_name":"7","id":"rs1258545451","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471203,"source":"dbSNP","strand":1,"feature_type":"variation","end":140471203,"alleles":["T","C"]},{"end":140471204,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140471204,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1221869808","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471209,"feature_type":"variation","strand":1,"end":140471209,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1442952023"},{"source":"dbSNP","start":140471210,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140471210,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1271113851"},{"source":"dbSNP","start":140471211,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140471211,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585490474"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471212,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140471212,"id":"rs1433379474","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs984624350","seq_region_name":"7","feature_type":"variation","strand":1,"end":140471213,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471213},{"source":"dbSNP","start":140471218,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140471218,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794913551"},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140471221,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471221,"clinical_significance":[],"id":"rs1030576616","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs961965373","alleles":["AAAAAA","AAAAA","AAAAAAA"],"end":140471227,"feature_type":"variation","strand":1,"source":"dbSNP","start":140471222,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1178009944","clinical_significance":[],"start":140471225,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140471225,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471227,"source":"dbSNP","strand":1,"feature_type":"variation","end":140471227,"alleles":["A","T"],"seq_region_name":"7","id":"rs532983779","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130340780","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471229,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140471229},{"clinical_significance":[],"seq_region_name":"7","id":"rs1412353923","alleles":["A","G"],"end":140471236,"feature_type":"variation","strand":1,"source":"dbSNP","start":140471236,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794914101","alleles":["G","A"],"end":140471238,"feature_type":"variation","strand":1,"source":"dbSNP","start":140471238,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140471241,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140471241,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794914183","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585490515","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471241,"feature_type":"variation","strand":1,"end":140471243,"alleles":["GTG","G"]},{"id":"rs772444945","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471244,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140471244},{"start":140471246,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140471246,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs551560993","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794914566","end":140471250,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140471250,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140471254,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471254,"clinical_significance":[],"seq_region_name":"7","id":"rs1794914641"},{"clinical_significance":[],"id":"rs923161675","seq_region_name":"7","feature_type":"variation","strand":1,"end":140471256,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471256},{"clinical_significance":[],"seq_region_name":"7","id":"rs1007230853","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471257,"feature_type":"variation","strand":1,"end":140471257,"alleles":["G","T"]},{"strand":1,"feature_type":"variation","end":140471259,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471259,"source":"dbSNP","seq_region_name":"7","id":"rs933364495","clinical_significance":[]},{"start":140471262,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140471262,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","id":"rs1449223515","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471267,"source":"dbSNP","strand":1,"feature_type":"variation","end":140471267,"alleles":["C","A","T"],"id":"rs1461734360","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471270,"source":"dbSNP","strand":1,"feature_type":"variation","end":140471270,"alleles":["G","C"],"seq_region_name":"7","id":"rs1265029950","clinical_significance":[]},{"seq_region_name":"7","id":"rs1304900458","clinical_significance":[],"end":140471273,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140471273,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471274,"source":"dbSNP","strand":1,"feature_type":"variation","end":140471274,"alleles":["G","A"],"seq_region_name":"7","id":"rs1311793750","clinical_significance":[]},{"id":"rs7811221","seq_region_name":"7","clinical_significance":[],"end":140471276,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140471276,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["T","G"],"end":140471277,"strand":1,"feature_type":"variation","start":140471277,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794915748","clinical_significance":[]},{"id":"rs1936468360","seq_region_name":"7","clinical_significance":[],"start":140471278,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140471278,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1794915838","clinical_significance":[],"strand":1,"feature_type":"variation","end":140471280,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471280,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140471283,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471283,"source":"dbSNP","seq_region_name":"7","id":"rs1216677846","clinical_significance":[]},{"seq_region_name":"7","id":"rs1360242345","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471284,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140471284},{"clinical_significance":[],"seq_region_name":"7","id":"rs547969694","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471285,"feature_type":"variation","strand":1,"end":140471285,"alleles":["G","C"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471287,"feature_type":"variation","strand":1,"end":140471287,"alleles":["G","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794916203"},{"start":140471289,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140471289,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794916289","clinical_significance":[]},{"seq_region_name":"7","id":"rs936725229","clinical_significance":[],"alleles":["C","T"],"end":140471291,"strand":1,"feature_type":"variation","start":140471291,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1794916480","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140471297,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471297},{"id":"rs978635385","seq_region_name":"7","clinical_significance":[],"start":140471300,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140471300,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471302,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140471302,"seq_region_name":"7","id":"rs1794916659","clinical_significance":[]},{"seq_region_name":"7","id":"rs1385653193","clinical_significance":[],"start":140471303,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140471303,"strand":1,"feature_type":"variation"},{"start":140471307,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C"],"end":140471307,"strand":1,"feature_type":"variation","id":"rs1297838288","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794916943","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471310,"source":"dbSNP","strand":1,"feature_type":"variation","end":140471310,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1794917027","clinical_significance":[],"end":140471313,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140471313,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140471319,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140471319,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1338108359"},{"seq_region_name":"7","id":"rs1445230779","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140471320,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471320,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1794917240","clinical_significance":[],"alleles":["G","A"],"end":140471323,"strand":1,"feature_type":"variation","start":140471323,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140471325,"alleles":["AA","A"],"strand":1,"feature_type":"variation","start":140471324,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794917322","clinical_significance":[]},{"id":"rs1585490659","seq_region_name":"7","clinical_significance":[],"alleles":["G","C"],"end":140471326,"strand":1,"feature_type":"variation","start":140471326,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1585490670","clinical_significance":[],"alleles":["G","-"],"end":140471328,"strand":1,"feature_type":"variation","start":140471328,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140471328,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140471328,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794917496"},{"source":"dbSNP","start":140471329,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140471329,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1366810517"},{"alleles":["C","T"],"end":140471330,"strand":1,"feature_type":"variation","start":140471330,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1794917760","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130341313","clinical_significance":[],"alleles":["A","T"],"end":140471332,"strand":1,"feature_type":"variation","start":140471332,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1031893460","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471333,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140471333},{"source":"dbSNP","start":140471334,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140471334,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794917969"},{"seq_region_name":"7","id":"rs775943360","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471335,"source":"dbSNP","strand":1,"feature_type":"variation","end":140471335,"alleles":["C","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471340,"source":"dbSNP","strand":1,"feature_type":"variation","end":140471340,"alleles":["G","A"],"id":"rs1411300619","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794918220","clinical_significance":[],"alleles":["A","C"],"end":140471342,"strand":1,"feature_type":"variation","start":140471342,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1388044892","clinical_significance":[],"end":140471343,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140471343,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140471345,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140471345,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs955885283"},{"id":"rs1167750483","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140471355,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471355,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794918568","end":140471357,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140471357,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["C","A","G"],"end":140471360,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471360,"source":"dbSNP","seq_region_name":"7","id":"rs1244935823","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1180186964","end":140471364,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140471364,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794919434","feature_type":"variation","strand":1,"end":140471366,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471366},{"seq_region_name":"7","id":"rs147072972","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471368,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140471368},{"clinical_significance":[],"id":"rs1794919625","seq_region_name":"7","end":140471369,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140471369,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140471372,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140471372,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs892614132"},{"clinical_significance":[],"id":"rs1794919810","seq_region_name":"7","source":"dbSNP","start":140471374,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140471374,"feature_type":"variation","strand":1},{"start":140471377,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140471383,"alleles":["AAAAAAA","AAAAAAAA"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1211999908","clinical_significance":[]},{"start":140471379,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140471379,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs531129596","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1253980410","alleles":["AAATAAATAAA","AAATAAA"],"end":140471391,"feature_type":"variation","strand":1,"source":"dbSNP","start":140471381,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140471383,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140471383,"alleles":["A","C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs113270948"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471388,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140471388,"clinical_significance":[],"id":"rs1794920339","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs879699257","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471389,"feature_type":"variation","strand":1,"end":140471394,"alleles":["AAAAAA","AAA"]},{"alleles":["A","G"],"end":140471391,"feature_type":"variation","strand":1,"source":"dbSNP","start":140471391,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1794920501","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794920594","feature_type":"variation","strand":1,"end":140471392,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471392},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794920665","end":140471394,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140471394,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471399,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140471399,"id":"rs763555036","seq_region_name":"7","clinical_significance":[]},{"start":140471405,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140471405,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794920859","clinical_significance":[]},{"start":140471407,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TTACTT","TT"],"end":140471412,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1313648063","clinical_significance":[]},{"source":"dbSNP","start":140471412,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140471412,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130341685"},{"seq_region_name":"7","id":"rs1794921028","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471424,"source":"dbSNP","strand":1,"feature_type":"variation","end":140471424,"alleles":["A","G"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471425,"feature_type":"variation","strand":1,"end":140471425,"alleles":["C","T"],"clinical_significance":[],"id":"rs1794921103","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471427,"source":"dbSNP","strand":1,"feature_type":"variation","end":140471427,"alleles":["G","A","T"],"id":"rs970735077","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794921258","clinical_significance":[],"start":140471427,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["GAT","-"],"end":140471429,"strand":1,"feature_type":"variation"},{"id":"rs1046674896","seq_region_name":"7","clinical_significance":[],"end":140471434,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140471434,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs773007458","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471436,"feature_type":"variation","strand":1,"end":140471436,"alleles":["C","A"]},{"end":140471437,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140471437,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs763017092","clinical_significance":[]},{"source":"dbSNP","start":140471440,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140471440,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1233317865"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471446,"feature_type":"variation","strand":1,"end":140471446,"alleles":["T","C"],"clinical_significance":[],"id":"rs1585490826","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1248872059","clinical_significance":[],"start":140471453,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140471453,"alleles":["T","C","G"],"strand":1,"feature_type":"variation"},{"start":140471457,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140471457,"strand":1,"feature_type":"variation","id":"rs1794921898","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794921996","end":140471459,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140471459,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140471460,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471460,"clinical_significance":[],"seq_region_name":"7","id":"rs770648015"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140471461,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471461,"source":"dbSNP","seq_region_name":"7","id":"rs942087962","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794922286","clinical_significance":[],"end":140471463,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140471463,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140471467,"alleles":["AAAA","AAAAA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471464,"source":"dbSNP","seq_region_name":"7","id":"rs796181302","clinical_significance":[]},{"start":140471469,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","T"],"end":140471469,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs769277543","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140471471,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471471,"source":"dbSNP","seq_region_name":"7","id":"rs1585490857","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794922714","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471471,"feature_type":"variation","strand":1,"alleles":["CTAC","CTACTAC"],"end":140471474},{"seq_region_name":"7","id":"rs1794922808","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471472,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140471472},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471474,"source":"dbSNP","strand":1,"feature_type":"variation","end":140471476,"alleles":["CCC","CCCC"],"seq_region_name":"7","id":"rs1425139223","clinical_significance":[]},{"seq_region_name":"7","id":"rs1184792455","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471477,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AA","A"],"end":140471478},{"id":"rs1563095162","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471478,"source":"dbSNP","strand":1,"feature_type":"variation","end":140471478,"alleles":["A","G","T"]},{"source":"dbSNP","start":140471479,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140471479,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1037889084"},{"seq_region_name":"7","id":"rs1162530220","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471479,"source":"dbSNP","strand":1,"feature_type":"variation","end":140471487,"alleles":["TTTTTTTTT","TTTTTT","TTTTTTTT","TTTTTTTTTT"]},{"end":140471482,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140471482,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs919449653","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471483,"source":"dbSNP","strand":1,"feature_type":"variation","end":140471483,"alleles":["T","G"],"seq_region_name":"7","id":"rs1794923577","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs567667652","source":"dbSNP","start":140471485,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140471485,"feature_type":"variation","strand":1},{"id":"rs1408760229","seq_region_name":"7","clinical_significance":[],"start":140471490,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["GG","-"],"end":140471491,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1419443687","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471490,"feature_type":"variation","strand":1,"alleles":["GGTGG","G"],"end":140471494},{"seq_region_name":"7","id":"rs774149297","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140471491,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471491,"source":"dbSNP"},{"alleles":["T","C"],"end":140471492,"feature_type":"variation","strand":1,"source":"dbSNP","start":140471492,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs894234864"},{"source":"dbSNP","start":140471493,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140471493,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1005946104"},{"source":"dbSNP","start":140471494,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["-","CA"],"end":140471493,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1415498712","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471496,"feature_type":"variation","strand":1,"end":140471496,"alleles":["G","C"],"clinical_significance":[],"id":"rs1794924299","seq_region_name":"7"},{"alleles":["C","A","T"],"end":140471500,"feature_type":"variation","strand":1,"source":"dbSNP","start":140471500,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1052056545"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471501,"source":"dbSNP","strand":1,"feature_type":"variation","end":140471501,"alleles":["G","A","C"],"seq_region_name":"7","id":"rs890704709","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794924616","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140471504,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471504},{"feature_type":"variation","strand":1,"alleles":["C","-"],"end":140471504,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471504,"clinical_significance":[],"id":"rs1794924706","seq_region_name":"7"},{"start":140471511,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140471511,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs961895531","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs767150753","end":140471515,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140471515,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs148139968","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140471517,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471517,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs553717375","source":"dbSNP","start":140471519,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140471519,"feature_type":"variation","strand":1},{"start":140471521,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140471521,"alleles":["G","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1320890798","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs7811669","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471522,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140471522},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471523,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140471523,"clinical_significance":[],"seq_region_name":"7","id":"rs910523780"},{"start":140471525,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140471525,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794925475","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130342314","clinical_significance":[],"start":140471530,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140471530,"strand":1,"feature_type":"variation"},{"id":"rs767189745","seq_region_name":"7","clinical_significance":[],"start":140471531,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140471531,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"alleles":["G","A"],"end":140471532,"feature_type":"variation","strand":1,"source":"dbSNP","start":140471532,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1031399914"},{"clinical_significance":[],"seq_region_name":"7","id":"rs936779337","source":"dbSNP","start":140471536,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140471536,"alleles":["C","T"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471537,"source":"dbSNP","strand":1,"feature_type":"variation","end":140471537,"alleles":["T","C"],"seq_region_name":"7","id":"rs752434814","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471543,"feature_type":"variation","strand":1,"end":140471543,"alleles":["C","T"],"clinical_significance":[],"id":"rs1794925838","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1585490979","clinical_significance":[],"start":140471544,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140471544,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130342391","source":"dbSNP","start":140471545,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140471545,"feature_type":"variation","strand":1},{"start":140471546,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140471546,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs913976840","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","G"],"end":140471553,"strand":1,"feature_type":"variation","start":140471553,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1161343629","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140471555,"alleles":["CC","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471554,"source":"dbSNP","id":"rs569336280","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140471555,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140471555,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1411496667"},{"id":"rs1585491007","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140471556,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471556,"source":"dbSNP"},{"source":"dbSNP","start":140471557,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140471557,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs955911897"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1200318036","feature_type":"variation","strand":1,"alleles":["CC","CCC"],"end":140471558,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471557},{"feature_type":"variation","strand":1,"end":140471562,"alleles":["C","A","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471562,"clinical_significance":[],"seq_region_name":"7","id":"rs1265646393"},{"seq_region_name":"7","id":"rs370763087","clinical_significance":[],"strand":1,"feature_type":"variation","end":140471563,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471563,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140471565,"alleles":["GGG","GG"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471563,"source":"dbSNP","seq_region_name":"7","id":"rs762844109","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140471565,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471565,"source":"dbSNP","seq_region_name":"7","id":"rs1263086188","clinical_significance":[]},{"alleles":["T","G"],"end":140471566,"strand":1,"feature_type":"variation","start":140471566,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585491049","clinical_significance":[]},{"source":"dbSNP","start":140471577,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["CTCCT","CT"],"end":140471581,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794927215"},{"id":"rs1794927315","seq_region_name":"7","clinical_significance":[],"start":140471578,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140471578,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471580,"feature_type":"variation","strand":1,"end":140471580,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs539256705"},{"source":"dbSNP","start":140471582,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140471582,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794927501"},{"start":140471585,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140471585,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794927586","clinical_significance":[]},{"source":"dbSNP","start":140471591,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140471591,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794927664"},{"strand":1,"feature_type":"variation","end":140471593,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471593,"source":"dbSNP","seq_region_name":"7","id":"rs1585491062","clinical_significance":[]},{"clinical_significance":[],"id":"rs1024182695","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471594,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140471594},{"strand":1,"feature_type":"variation","end":140471597,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471597,"source":"dbSNP","seq_region_name":"7","id":"rs1794927934","clinical_significance":[]},{"seq_region_name":"7","id":"rs1326389158","clinical_significance":[],"strand":1,"feature_type":"variation","end":140471602,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471602,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471604,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140471604,"seq_region_name":"7","id":"rs969907106","clinical_significance":[]},{"seq_region_name":"7","id":"rs980816451","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140471605,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471605,"source":"dbSNP"},{"id":"rs1332486231","seq_region_name":"7","clinical_significance":[],"start":140471608,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140471608,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140471610,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140471610,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1220910557"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130342709","source":"dbSNP","start":140471610,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["CAGACGCACACCA","CA"],"end":140471622,"feature_type":"variation","strand":1},{"alleles":["A","T"],"end":140471611,"strand":1,"feature_type":"variation","start":140471611,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794928554","clinical_significance":[]},{"clinical_significance":[],"id":"rs938226050","seq_region_name":"7","source":"dbSNP","start":140471612,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140471612,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140471614,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471614,"clinical_significance":[],"seq_region_name":"7","id":"rs557559576"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471615,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140471615,"clinical_significance":[],"id":"rs1362572423","seq_region_name":"7"},{"seq_region_name":"7","id":"rs963399261","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140471616,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471616,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563095257","alleles":["CACACCAC","C"],"end":140471623,"feature_type":"variation","strand":1,"source":"dbSNP","start":140471616,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140471620,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471620,"source":"dbSNP","seq_region_name":"7","id":"rs576133629","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1209120872","source":"dbSNP","start":140471621,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140471621,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1471064318","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471624,"source":"dbSNP","strand":1,"feature_type":"variation","end":140471624,"alleles":["C","T"]},{"alleles":["T","C"],"end":140471626,"strand":1,"feature_type":"variation","start":140471626,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1376172652","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794930022","clinical_significance":[],"alleles":["C","A"],"end":140471628,"strand":1,"feature_type":"variation","start":140471628,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140471629,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471629,"source":"dbSNP","seq_region_name":"7","id":"rs1794930095","clinical_significance":[]},{"id":"rs150267428","seq_region_name":"7","clinical_significance":[],"alleles":["A","C"],"end":140471631,"strand":1,"feature_type":"variation","start":140471631,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140471633,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140471633,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1198589992","clinical_significance":[]},{"end":140471635,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140471635,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs973921720","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140471639,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471639,"clinical_significance":[],"id":"rs2130342893","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs760083070","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471644,"feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140471644},{"start":140471645,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140471645,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794930588","clinical_significance":[]},{"end":140471647,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140471647,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1794930667","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794930745","alleles":["G","A"],"end":140471651,"feature_type":"variation","strand":1,"source":"dbSNP","start":140471651,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140471652,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140471652,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1466378740","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1187152588","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471657,"source":"dbSNP","strand":1,"feature_type":"variation","end":140471657,"alleles":["A","G"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471659,"source":"dbSNP","strand":1,"feature_type":"variation","end":140471659,"alleles":["G","A"],"seq_region_name":"7","id":"rs1585491180","clinical_significance":[]},{"alleles":["G","C"],"end":140471661,"feature_type":"variation","strand":1,"source":"dbSNP","start":140471661,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs554904921","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140471663,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471663,"clinical_significance":[],"id":"rs573319509","seq_region_name":"7"},{"source":"dbSNP","start":140471668,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140471668,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs2130343003","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1794931297","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471671,"source":"dbSNP","strand":1,"feature_type":"variation","end":140471671,"alleles":["G","A","C"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471672,"source":"dbSNP","strand":1,"feature_type":"variation","end":140471672,"alleles":["G","A"],"seq_region_name":"7","id":"rs1464866619","clinical_significance":[]},{"seq_region_name":"7","id":"rs1213764736","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471676,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140471676},{"start":140471680,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140471680,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs929495899","clinical_significance":[]},{"clinical_significance":[],"id":"rs1585491208","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140471685,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471685},{"seq_region_name":"7","id":"rs1051900065","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471697,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140471697},{"seq_region_name":"7","id":"rs2130343075","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471701,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140471701},{"seq_region_name":"7","id":"rs1241555813","clinical_significance":[],"alleles":["T","G"],"end":140471702,"strand":1,"feature_type":"variation","start":140471702,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471712,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140471712,"clinical_significance":[],"id":"rs1346649926","seq_region_name":"7"},{"seq_region_name":"7","id":"rs374173810","clinical_significance":[],"start":140471718,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140471718,"alleles":["C","A","T"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471719,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140471719,"seq_region_name":"7","id":"rs1478379020","clinical_significance":[]},{"alleles":["A","T"],"end":140471722,"strand":1,"feature_type":"variation","start":140471722,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1005872054","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1232246179","seq_region_name":"7","feature_type":"variation","strand":1,"end":140471723,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471723},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471727,"feature_type":"variation","strand":1,"end":140471727,"alleles":["C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs12537112"},{"id":"rs1794932559","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140471729,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471729,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471730,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140471730,"clinical_significance":[],"id":"rs2130343205","seq_region_name":"7"},{"id":"rs1794932651","seq_region_name":"7","clinical_significance":[],"start":140471733,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140471733,"strand":1,"feature_type":"variation"},{"end":140471736,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140471736,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1299580131","clinical_significance":[]},{"clinical_significance":[],"id":"rs1432744534","seq_region_name":"7","feature_type":"variation","strand":1,"end":140471738,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471738},{"feature_type":"variation","strand":1,"end":140471739,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471739,"clinical_significance":[],"seq_region_name":"7","id":"rs1364430888"},{"source":"dbSNP","start":140471745,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140471745,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs559249045","seq_region_name":"7"},{"start":140471746,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140471746,"alleles":["A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs376672992","clinical_significance":[]},{"seq_region_name":"7","id":"rs897560529","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471747,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140471747},{"alleles":["G","A"],"end":140471748,"strand":1,"feature_type":"variation","start":140471748,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130343314","clinical_significance":[]},{"clinical_significance":[],"id":"rs1794933318","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471754,"feature_type":"variation","strand":1,"end":140471754,"alleles":["G","C"]},{"seq_region_name":"7","id":"rs1794933410","clinical_significance":[],"start":140471756,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","T"],"end":140471756,"strand":1,"feature_type":"variation"},{"id":"rs943571830","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140471757,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471757,"source":"dbSNP"},{"start":140471758,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140471758,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1400316644","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471763,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140471763,"clinical_significance":[],"seq_region_name":"7","id":"rs1794933713"},{"id":"rs1794933807","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140471765,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471765,"source":"dbSNP"},{"alleles":["C","G"],"end":140471767,"strand":1,"feature_type":"variation","start":140471767,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1172145578","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140471769,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471769,"source":"dbSNP","seq_region_name":"7","id":"rs1794933986","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471772,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140471772,"seq_region_name":"7","id":"rs1462700142","clinical_significance":[]},{"clinical_significance":[],"id":"rs1794934166","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140471774,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471774},{"seq_region_name":"7","id":"rs2130343459","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471775,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140471775},{"alleles":["T","C"],"end":140471787,"strand":1,"feature_type":"variation","start":140471787,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1039274405","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794934256","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471789,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140471789},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471790,"feature_type":"variation","strand":1,"end":140471790,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1167132638"},{"start":140471790,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TTTTT","TTTT"],"end":140471794,"strand":1,"feature_type":"variation","id":"rs1480315657","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs532943384","clinical_significance":[],"start":140471791,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140471791,"alleles":["T","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130343531","end":140471800,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140471800,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794934511","end":140471804,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140471804,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140471807,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140471807,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130343561","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1160288710","feature_type":"variation","strand":1,"alleles":["T","TT"],"end":140471808,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471808},{"seq_region_name":"7","id":"rs1794934667","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471808,"source":"dbSNP","strand":1,"feature_type":"variation","end":140471808,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs999861788","clinical_significance":[],"end":140471819,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140471819,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1183650958","seq_region_name":"7","source":"dbSNP","start":140471823,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TAT","T"],"end":140471825,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs747393464","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471824,"feature_type":"variation","strand":1,"end":140471824,"alleles":["A","G","T"]},{"seq_region_name":"7","id":"rs1053312340","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140471826,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471826,"source":"dbSNP"},{"id":"rs1794935324","seq_region_name":"7","clinical_significance":[],"start":140471827,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A","C"],"end":140471827,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs369383734","seq_region_name":"7","source":"dbSNP","start":140471831,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140471831,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs2130343691","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471835,"feature_type":"variation","strand":1,"end":140471835,"alleles":["C","A"]},{"clinical_significance":[],"id":"rs138927547","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471836,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140471836},{"clinical_significance":[],"id":"rs1394301642","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140471843,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471843},{"seq_region_name":"7","id":"rs745791313","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471846,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140471846},{"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140471850,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471850,"source":"dbSNP","seq_region_name":"7","id":"rs756172762","clinical_significance":[]},{"start":140471852,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140471852,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs779870354","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140471855,"alleles":["CCCC","CCCCC"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471852,"clinical_significance":[],"id":"rs753238796","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1317761482","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471853,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140471853},{"clinical_significance":[],"seq_region_name":"7","id":"rs749056281","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471855,"feature_type":"variation","strand":1,"end":140471855,"alleles":["C","G"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140471856,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140471856,"seq_region_name":"7","id":"rs1794936466","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1014043455","alleles":["C","G","T"],"end":140471860,"feature_type":"variation","strand":1,"source":"dbSNP","start":140471860,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794936658","feature_type":"variation","strand":1,"end":140471866,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471866},{"clinical_significance":[],"id":"rs563624738","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471872,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140471872},{"source":"dbSNP","start":140471875,"consequence_type":"splice_region_variant","assembly_name":"GRCh38","end":140471875,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs747860651","seq_region_name":"7"},{"source":"dbSNP","start":140471877,"consequence_type":"splice_donor_region_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140471877,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs771557348"},{"alleles":["T","A"],"end":140471879,"strand":1,"feature_type":"variation","start":140471879,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_donor_region_variant","seq_region_name":"7","id":"rs374897484","clinical_significance":[]},{"clinical_significance":[],"id":"rs1172444012","seq_region_name":"7","source":"dbSNP","start":140471883,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140471883,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140471886,"alleles":["C","T"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471886,"clinical_significance":[],"seq_region_name":"7","id":"rs761138220"},{"alleles":["G","A"],"end":140471888,"feature_type":"variation","strand":1,"source":"dbSNP","start":140471888,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs969962959"},{"seq_region_name":"7","id":"rs142266018","clinical_significance":[],"start":140471889,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["C","A","T"],"end":140471889,"strand":1,"feature_type":"variation"},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471890,"feature_type":"variation","strand":1,"end":140471890,"alleles":["G","A","C","T"],"clinical_significance":[],"id":"rs759833443","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140471891,"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140471891,"source":"dbSNP","id":"rs368299978","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1016834959","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","A"],"end":140471892,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471892},{"clinical_significance":[],"seq_region_name":"7","id":"rs752963204","end":140471893,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140471893,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs963749977","source":"dbSNP","start":140471898,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140471898,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1362812980","clinical_significance":[],"strand":1,"feature_type":"variation","end":140471904,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140471904,"source":"dbSNP"},{"clinical_significance":[],"id":"rs763329575","seq_region_name":"7","alleles":["A","C"],"end":140471908,"feature_type":"variation","strand":1,"source":"dbSNP","start":140471908,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs189177147","end":140471909,"alleles":["C","A","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140471909,"consequence_type":"synonymous_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140471910,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140471910,"source":"dbSNP","seq_region_name":"7","id":"rs1340127667","clinical_significance":[]},{"seq_region_name":"7","id":"rs1366164789","clinical_significance":[],"strand":1,"feature_type":"variation","end":140471912,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140471912,"source":"dbSNP"},{"id":"rs145220948","seq_region_name":"7","clinical_significance":[],"end":140471913,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140471913,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794938902","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471916,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140471916},{"clinical_significance":["uncertain significance"],"seq_region_name":"7","id":"rs148479842","end":140471917,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140471917,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1794939043","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140471928,"source":"dbSNP","strand":1,"feature_type":"variation","end":140471928,"alleles":["C","A"]},{"source":"dbSNP","start":140471929,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140471929,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794939120"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1310919085","end":140471931,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140471931,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1794939269","clinical_significance":["uncertain significance"],"start":140471932,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140471932,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"end":140471936,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140471936,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794939329"},{"clinical_significance":[],"seq_region_name":"7","id":"rs756041794","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471937,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140471937},{"seq_region_name":"7","id":"rs1794939467","clinical_significance":[],"alleles":["A","T"],"end":140471941,"strand":1,"feature_type":"variation","start":140471941,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"start":140471942,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","alleles":["C","A","T"],"end":140471942,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs11556754","clinical_significance":[]},{"alleles":["G","A","C"],"end":140471943,"strand":1,"feature_type":"variation","start":140471943,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","id":"rs528516903","seq_region_name":"7","clinical_significance":["uncertain significance"]},{"seq_region_name":"7","id":"rs547299372","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140471945,"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140471945,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1202759091","clinical_significance":[],"strand":1,"feature_type":"variation","end":140471947,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140471947,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs771751617","source":"dbSNP","start":140471948,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140471948,"feature_type":"variation","strand":1},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471956,"feature_type":"variation","strand":1,"end":140471956,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs777223427"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1191511437","source":"dbSNP","start":140471957,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","end":140471957,"alleles":["G","A"],"feature_type":"variation","strand":1},{"start":140471960,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140471960,"alleles":["A","C"],"strand":1,"feature_type":"variation","id":"rs1794940016","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471961,"feature_type":"variation","strand":1,"end":140471961,"alleles":["T","A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs746543306"},{"seq_region_name":"7","id":"rs771413369","clinical_significance":[],"alleles":["C","A","T"],"end":140471963,"strand":1,"feature_type":"variation","start":140471963,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant"},{"start":140471964,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140471964,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs760157410","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140471965,"alleles":["A","T"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471965,"clinical_significance":[],"seq_region_name":"7","id":"rs1361247050"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1421524839","alleles":["G","A"],"end":140471966,"feature_type":"variation","strand":1,"source":"dbSNP","start":140471966,"consequence_type":"synonymous_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1794940562","seq_region_name":"7","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471967,"feature_type":"variation","strand":1,"end":140471967,"alleles":["T","C"]},{"end":140471969,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140471969,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1296437744"},{"clinical_significance":[],"seq_region_name":"7","id":"rs770042700","end":140471970,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140471970,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs371054341","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140471971,"source":"dbSNP","strand":1,"feature_type":"variation","end":140471971,"alleles":["G","A","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1354202081","alleles":["A","G"],"end":140471972,"feature_type":"variation","strand":1,"source":"dbSNP","start":140471972,"consequence_type":"synonymous_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1794941213","clinical_significance":[],"alleles":["C","G"],"end":140471973,"strand":1,"feature_type":"variation","start":140471973,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140471975,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140471975,"source":"dbSNP","id":"rs1283641772","seq_region_name":"7","clinical_significance":[]},{"end":140471979,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140471979,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794941439"},{"strand":1,"feature_type":"variation","end":140471980,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140471980,"source":"dbSNP","seq_region_name":"7","id":"rs764444396","clinical_significance":["uncertain significance"]},{"seq_region_name":"7","id":"rs1344379260","clinical_significance":[],"end":140471982,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140471982,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"end":140471983,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140471983,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs1794941790","clinical_significance":[]},{"id":"rs142729794","seq_region_name":"7","clinical_significance":[],"end":140471984,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140471984,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant"},{"id":"rs928091301","seq_region_name":"7","clinical_significance":[],"start":140471990,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","end":140471990,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"alleles":["A","C","G"],"end":140471993,"strand":1,"feature_type":"variation","start":140471993,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","seq_region_name":"7","id":"rs761801209","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs938295103","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140471995,"feature_type":"variation","strand":1,"end":140471995,"alleles":["C","T"]},{"id":"rs767699720","seq_region_name":"7","clinical_significance":[],"start":140471996,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","alleles":["C","T"],"end":140471996,"strand":1,"feature_type":"variation"},{"start":140471999,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","alleles":["A","G"],"end":140471999,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1356483503","clinical_significance":[]},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472000,"feature_type":"variation","strand":1,"end":140472000,"alleles":["T","C"],"clinical_significance":["uncertain significance"],"seq_region_name":"7","id":"rs572012392"},{"start":140472003,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["A","G"],"end":140472003,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs754992132","clinical_significance":[]},{"start":140472013,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_acceptor_variant","end":140472013,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs2130344899","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","A"],"end":140472014,"feature_type":"variation","strand":1,"source":"dbSNP","start":140472014,"consequence_type":"splice_region_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs778646668"},{"clinical_significance":[],"id":"rs1563095463","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140472017,"consequence_type":"splice_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472017},{"alleles":["G","A"],"end":140472018,"strand":1,"feature_type":"variation","start":140472018,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_region_variant","seq_region_name":"7","id":"rs1794943125","clinical_significance":[]},{"end":140472020,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140472020,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_polypyrimidine_tract_variant","id":"rs752518959","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs779371407","end":140472021,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140472021,"consequence_type":"splice_polypyrimidine_tract_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs750845113","seq_region_name":"7","consequence_type":"splice_polypyrimidine_tract_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472022,"feature_type":"variation","strand":1,"end":140472022,"alleles":["A","G"]},{"assembly_name":"GRCh38","consequence_type":"splice_polypyrimidine_tract_variant","start":140472022,"source":"dbSNP","strand":1,"feature_type":"variation","end":140472024,"alleles":["AAA","AAAA"],"seq_region_name":"7","id":"rs1794943393","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130344998","clinical_significance":[],"start":140472024,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_polypyrimidine_tract_variant","end":140472026,"alleles":["AGA","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1794943446","seq_region_name":"7","end":140472027,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140472027,"consequence_type":"splice_polypyrimidine_tract_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794943496","end":140472029,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140472029,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1476959578","source":"dbSNP","start":140472030,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140472030,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140472035,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140472035,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794943594"},{"clinical_significance":[],"seq_region_name":"7","id":"rs777418168","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472037,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140472037},{"seq_region_name":"7","id":"rs758664278","clinical_significance":[],"alleles":["GG","G"],"end":140472038,"strand":1,"feature_type":"variation","start":140472037,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs750075580","clinical_significance":[],"start":140472038,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140472038,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"start":140472045,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140472045,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs746462989","clinical_significance":[]},{"source":"dbSNP","start":140472046,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140472046,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs756718847","seq_region_name":"7"},{"id":"rs780813440","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472048,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140472048},{"seq_region_name":"7","id":"rs374316963","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140472050,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472050,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1794944047","clinical_significance":[],"end":140472052,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140472052,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472054,"feature_type":"variation","strand":1,"end":140472054,"alleles":["T","C"],"clinical_significance":[],"id":"rs1325852334","seq_region_name":"7"},{"source":"dbSNP","start":140472055,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140472055,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1348363278","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140472059,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472059,"clinical_significance":[],"seq_region_name":"7","id":"rs770376927"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472061,"source":"dbSNP","strand":1,"feature_type":"variation","end":140472061,"alleles":["A","G"],"seq_region_name":"7","id":"rs1794944258","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794944299","clinical_significance":[],"alleles":["T","C","G"],"end":140472069,"strand":1,"feature_type":"variation","start":140472069,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794944378","feature_type":"variation","strand":1,"end":140472071,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472071},{"alleles":["T","G"],"end":140472073,"strand":1,"feature_type":"variation","start":140472073,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794944466","clinical_significance":[]},{"id":"rs535176999","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140472075,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472075,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140472078,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472078,"clinical_significance":[],"seq_region_name":"7","id":"rs1051622273"},{"id":"rs1794944780","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140472081,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472081,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472085,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140472085,"clinical_significance":[],"seq_region_name":"7","id":"rs1794944861"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1269283426","feature_type":"variation","strand":1,"end":140472095,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472095},{"start":140472100,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140472100,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1200784844","clinical_significance":[]},{"alleles":["G","A","C"],"end":140472101,"feature_type":"variation","strand":1,"source":"dbSNP","start":140472101,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs557483143"},{"alleles":["T","-"],"end":140472102,"strand":1,"feature_type":"variation","start":140472102,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1289129599","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794945257","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140472102,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472102,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1794945427","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472102,"source":"dbSNP","strand":1,"feature_type":"variation","end":140472107,"alleles":["TAAATA","TAAATAAATA"]},{"seq_region_name":"7","id":"rs1585491973","clinical_significance":[],"start":140472103,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140472103,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1007336123","clinical_significance":[],"start":140472105,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140472105,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140472107,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140472107,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794945678"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794945754","alleles":["ACACA","A"],"end":140472111,"feature_type":"variation","strand":1,"source":"dbSNP","start":140472107,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1331235464","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140472108,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472108,"source":"dbSNP"},{"id":"rs1794945930","seq_region_name":"7","clinical_significance":[],"end":140472114,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140472114,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140472118,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140472118,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs935671739","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs569362501","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140472119,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472119},{"clinical_significance":[],"id":"rs1794946228","seq_region_name":"7","source":"dbSNP","start":140472123,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140472123,"alleles":["T","A","C"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140472127,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472127,"source":"dbSNP","id":"rs1017510369","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140472129,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472129,"clinical_significance":[],"id":"rs372370683","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140472130,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472130,"source":"dbSNP","seq_region_name":"7","id":"rs1794946439","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472133,"source":"dbSNP","strand":1,"feature_type":"variation","end":140472133,"alleles":["G","C"],"seq_region_name":"7","id":"rs1490315263","clinical_significance":[]},{"seq_region_name":"7","id":"rs113573240","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140472134,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472134,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1794946723","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140472137,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472137},{"source":"dbSNP","start":140472138,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140472138,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1010863925"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794946918","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472138,"feature_type":"variation","strand":1,"end":140472153,"alleles":["GGCCAGGCATGGTGGC","GGC"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1021338792","source":"dbSNP","start":140472140,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140472140,"alleles":["C","A"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472145,"feature_type":"variation","strand":1,"end":140472145,"alleles":["C","A"],"clinical_significance":[],"id":"rs1794947094","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472146,"source":"dbSNP","strand":1,"feature_type":"variation","end":140472146,"alleles":["A","G"],"id":"rs1331031172","seq_region_name":"7","clinical_significance":[]},{"start":140472151,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140472151,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794947276","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140472152,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472152,"source":"dbSNP","seq_region_name":"7","id":"rs537117334","clinical_significance":[]},{"seq_region_name":"7","id":"rs1459298142","clinical_significance":[],"end":140472155,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140472155,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472156,"feature_type":"variation","strand":1,"end":140472156,"alleles":["A","T"],"clinical_significance":[],"id":"rs949774737","seq_region_name":"7"},{"end":140472160,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140472160,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794947589","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1468899942","source":"dbSNP","start":140472162,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140472162,"feature_type":"variation","strand":1},{"alleles":["C","T"],"end":140472168,"strand":1,"feature_type":"variation","start":140472168,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1794947744","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1794947818","seq_region_name":"7","feature_type":"variation","strand":1,"end":140472172,"alleles":["CAGT","CAGTCAGT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472169},{"alleles":["T","C"],"end":140472177,"strand":1,"feature_type":"variation","start":140472177,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1794947914","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472179,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140472179,"clinical_significance":[],"seq_region_name":"7","id":"rs1794947990"},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140472180,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472180,"clinical_significance":[],"seq_region_name":"7","id":"rs1390142486"},{"clinical_significance":[],"id":"rs1157691355","seq_region_name":"7","source":"dbSNP","start":140472181,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140472181,"alleles":["G","A"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140472182,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472182,"source":"dbSNP","id":"rs747310168","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs555067372","end":140472188,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140472188,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140472188,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140472191,"alleles":["AGGT","AGGTCAGGT"],"strand":1,"feature_type":"variation","id":"rs1794948422","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140472189,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140472189,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1406609572"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472191,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","TT"],"end":140472191,"id":"rs1794948620","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs966831303","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472192,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140472192},{"seq_region_name":"7","id":"rs1245913742","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140472194,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472194,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472195,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140472195,"seq_region_name":"7","id":"rs982579483","clinical_significance":[]},{"alleles":["C","T"],"end":140472200,"feature_type":"variation","strand":1,"source":"dbSNP","start":140472200,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1466212741","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472203,"source":"dbSNP","strand":1,"feature_type":"variation","end":140472203,"alleles":["C","G"],"seq_region_name":"7","id":"rs928052472","clinical_significance":[]},{"end":140472214,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140472214,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794949088"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472216,"feature_type":"variation","strand":1,"end":140472216,"alleles":["T","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794949135"},{"start":140472219,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140472219,"strand":1,"feature_type":"variation","id":"rs1208245334","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1324524110","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472221,"source":"dbSNP","strand":1,"feature_type":"variation","end":140472221,"alleles":["G","A"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472225,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140472225,"seq_region_name":"7","id":"rs1794949292","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794949343","feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140472227,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472227},{"clinical_significance":[],"seq_region_name":"7","id":"rs1001375152","end":140472228,"alleles":["G","A","C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140472228,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472231,"source":"dbSNP","strand":1,"feature_type":"variation","end":140472231,"alleles":["T","C"],"seq_region_name":"7","id":"rs1217695735","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472232,"source":"dbSNP","strand":1,"feature_type":"variation","end":140472232,"alleles":["C","T"],"seq_region_name":"7","id":"rs570183348","clinical_significance":[]},{"start":140472233,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140472233,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs959835165","clinical_significance":[]},{"alleles":["A","G"],"end":140472234,"strand":1,"feature_type":"variation","start":140472234,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs760327114","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794949659","source":"dbSNP","start":140472240,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140472240,"alleles":["G","A"],"feature_type":"variation","strand":1},{"alleles":["C","G"],"end":140472242,"strand":1,"feature_type":"variation","start":140472242,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794949746","clinical_significance":[]},{"end":140472243,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140472243,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794949830"},{"strand":1,"feature_type":"variation","end":140472246,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472246,"source":"dbSNP","seq_region_name":"7","id":"rs898379569","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472247,"source":"dbSNP","strand":1,"feature_type":"variation","end":140472247,"alleles":["C","A","T"],"seq_region_name":"7","id":"rs995249253","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140472249,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472249,"source":"dbSNP","id":"rs1794950050","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472250,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140472250,"clinical_significance":[],"seq_region_name":"7","id":"rs1026296269"},{"alleles":["T","C"],"end":140472252,"feature_type":"variation","strand":1,"source":"dbSNP","start":140472252,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794950165"},{"clinical_significance":[],"id":"rs950682164","seq_region_name":"7","feature_type":"variation","strand":1,"end":140472253,"alleles":["G","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472253},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472255,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140472255,"clinical_significance":[],"seq_region_name":"7","id":"rs1794950271"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472260,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140472260,"clinical_significance":[],"seq_region_name":"7","id":"rs987576525"},{"clinical_significance":[],"id":"rs1794950367","seq_region_name":"7","source":"dbSNP","start":140472262,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140472262,"alleles":["C","A"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472263,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140472263,"clinical_significance":[],"seq_region_name":"7","id":"rs1424141778"},{"end":140472264,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140472264,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1169017874"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472269,"feature_type":"variation","strand":1,"end":140472269,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794950542"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1019035562","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472271,"feature_type":"variation","strand":1,"alleles":["C","A","G"],"end":140472271},{"seq_region_name":"7","id":"rs201369563","clinical_significance":[],"strand":1,"feature_type":"variation","end":140472277,"alleles":["AAAAA","AAAA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472273,"source":"dbSNP"},{"start":140472277,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C","T"],"end":140472277,"strand":1,"feature_type":"variation","id":"rs965280097","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","T"],"end":140472279,"feature_type":"variation","strand":1,"source":"dbSNP","start":140472279,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585492268"},{"start":140472280,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140472280,"alleles":["C","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1208225410","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794951348","clinical_significance":[],"start":140472281,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140472281,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs974902042","feature_type":"variation","strand":1,"end":140472288,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472288},{"clinical_significance":[],"seq_region_name":"7","id":"rs928969390","alleles":["C","G","T"],"end":140472290,"feature_type":"variation","strand":1,"source":"dbSNP","start":140472290,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1051980958","seq_region_name":"7","source":"dbSNP","start":140472292,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140472292,"alleles":["G","T"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472294,"source":"dbSNP","strand":1,"feature_type":"variation","end":140472294,"alleles":["T","A","C"],"seq_region_name":"7","id":"rs890206046","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1289629565","source":"dbSNP","start":140472297,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140472297,"alleles":["G","C"],"feature_type":"variation","strand":1},{"alleles":["G","A","C"],"end":140472298,"feature_type":"variation","strand":1,"source":"dbSNP","start":140472298,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs943246567"},{"id":"rs1794951773","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140472299,"strand":1,"feature_type":"variation","start":140472299,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140472301,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140472301,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs753625864"},{"id":"rs1304098644","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140472305,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472305,"source":"dbSNP"},{"end":140472306,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140472306,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1445301180","clinical_significance":[]},{"end":140472307,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140472307,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs10267810","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1794952344","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472307,"source":"dbSNP","strand":1,"feature_type":"variation","end":140472308,"alleles":["AT","-"]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140472316,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472316,"source":"dbSNP","id":"rs988447166","seq_region_name":"7","clinical_significance":[]},{"end":140472317,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140472317,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs778798004"},{"seq_region_name":"7","id":"rs1794952549","clinical_significance":[],"start":140472319,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140472319,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1794952597","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472321,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140472321},{"end":140472322,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140472322,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1167823340","clinical_significance":[]},{"end":140472369,"alleles":["GGAGGCTGAGGCAGGAGAACTGCTTACACGTGGGAGGCTGAGG","GGAGGCTGAGG"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140472327,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1206558717","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472328,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140472328,"clinical_significance":[],"seq_region_name":"7","id":"rs1794952797"},{"seq_region_name":"7","id":"rs1794952849","clinical_significance":[],"start":140472330,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140472330,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140472334,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140472334,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs902535188","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140472336,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472336,"clinical_significance":[],"id":"rs141626150","seq_region_name":"7"},{"alleles":["A","G"],"end":140472339,"strand":1,"feature_type":"variation","start":140472339,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1794952967","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472340,"source":"dbSNP","strand":1,"feature_type":"variation","end":140472340,"alleles":["G","A"],"id":"rs144519594","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1181460104","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140472341,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472341,"source":"dbSNP"},{"clinical_significance":[],"id":"rs4726816","seq_region_name":"7","source":"dbSNP","start":140472346,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","G","T"],"end":140472346,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140472349,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140472349,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1482239327","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1473548944","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472350,"feature_type":"variation","strand":1,"end":140472350,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs990995801","source":"dbSNP","start":140472355,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140472355,"feature_type":"variation","strand":1},{"id":"rs1274384909","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472355,"source":"dbSNP","strand":1,"feature_type":"variation","end":140472356,"alleles":["CG","-"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs538640820","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472356,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140472356},{"seq_region_name":"7","id":"rs1226179446","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472360,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140472360},{"alleles":["T","C"],"end":140472365,"strand":1,"feature_type":"variation","start":140472365,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130346647","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794953726","alleles":["G","A"],"end":140472368,"feature_type":"variation","strand":1,"source":"dbSNP","start":140472368,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140472370,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140472370,"alleles":["T","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585492437"},{"seq_region_name":"7","id":"rs1429801061","clinical_significance":[],"start":140472371,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140472371,"alleles":["T","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1038169107","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472374,"source":"dbSNP","strand":1,"feature_type":"variation","end":140472374,"alleles":["A","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130346711","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472376,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140472376},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472379,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140472379,"seq_region_name":"7","id":"rs1288517862","clinical_significance":[]},{"source":"dbSNP","start":140472381,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140472381,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585492465"},{"id":"rs770880814","seq_region_name":"7","clinical_significance":[],"start":140472382,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140472382,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472385,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140472385,"seq_region_name":"7","id":"rs544975007","clinical_significance":[]},{"id":"rs1794954188","seq_region_name":"7","clinical_significance":[],"start":140472386,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140472386,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs774093832","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140472387,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472387},{"clinical_significance":[],"id":"rs1794954323","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472387,"feature_type":"variation","strand":1,"alleles":["CGCGC","CGC"],"end":140472391},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472388,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140472388,"clinical_significance":[],"seq_region_name":"7","id":"rs563455817"},{"end":140472389,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140472389,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs575364482","clinical_significance":[]},{"clinical_significance":[],"id":"rs543077713","seq_region_name":"7","feature_type":"variation","strand":1,"end":140472390,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472390},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472393,"feature_type":"variation","strand":1,"end":140472393,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1008894092"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472394,"source":"dbSNP","strand":1,"feature_type":"variation","end":140472394,"alleles":["T","C"],"seq_region_name":"7","id":"rs1019046850","clinical_significance":[]},{"id":"rs1794954733","seq_region_name":"7","clinical_significance":[],"start":140472398,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140472398,"strand":1,"feature_type":"variation"},{"alleles":["C","T"],"end":140472399,"strand":1,"feature_type":"variation","start":140472399,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs561402956","clinical_significance":[]},{"alleles":["C","A","T"],"end":140472405,"feature_type":"variation","strand":1,"source":"dbSNP","start":140472405,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs771952983","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140472419,"alleles":["CTGGGAGACAGAGC","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472406,"source":"dbSNP","seq_region_name":"7","id":"rs1794955024","clinical_significance":[]},{"start":140472410,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140472410,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs1412799198","seq_region_name":"7","clinical_significance":[]},{"start":140472414,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140472414,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794955234","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["AGAG","AG"],"end":140472418,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472415,"clinical_significance":[],"id":"rs1794955364","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1794955433","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472417,"source":"dbSNP","strand":1,"feature_type":"variation","end":140472417,"alleles":["A","C"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472423,"feature_type":"variation","strand":1,"end":140472423,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1184542243"},{"seq_region_name":"7","id":"rs1454815237","clinical_significance":[],"start":140472426,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140472426,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140472432,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140472432,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1471744481"},{"clinical_significance":[],"seq_region_name":"7","id":"rs911634997","source":"dbSNP","start":140472433,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AAAAAAAAAAAA","AAAAAAAAAAA","AAAAAAAAAAAAA"],"end":140472444,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs964785034","seq_region_name":"7","source":"dbSNP","start":140472438,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140472438,"alleles":["A","T"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140472439,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472439,"clinical_significance":[],"id":"rs59356360","seq_region_name":"7"},{"start":140472440,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140472440,"strand":1,"feature_type":"variation","id":"rs75808767","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs957756937","seq_region_name":"7","feature_type":"variation","strand":1,"end":140472441,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472441},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472443,"source":"dbSNP","strand":1,"feature_type":"variation","end":140472443,"alleles":["A","C"],"id":"rs1794956477","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1337956167","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472445,"feature_type":"variation","strand":1,"end":140472445,"alleles":["T","C","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs751309870","feature_type":"variation","strand":1,"end":140472450,"alleles":["AAAAA","AA","AAAAAA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472446},{"seq_region_name":"7","id":"rs1229809356","clinical_significance":[],"end":140472447,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140472447,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140472449,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140472449,"alleles":["A","C"],"strand":1,"feature_type":"variation","id":"rs1042726329","seq_region_name":"7","clinical_significance":[]},{"id":"rs1195614095","seq_region_name":"7","clinical_significance":[],"end":140472454,"alleles":["AAGAAG","AAG"],"strand":1,"feature_type":"variation","start":140472449,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1794957138","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472451,"source":"dbSNP","strand":1,"feature_type":"variation","end":140472451,"alleles":["G","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585492666","feature_type":"variation","strand":1,"end":140472456,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472456},{"strand":1,"feature_type":"variation","end":140472457,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472457,"source":"dbSNP","seq_region_name":"7","id":"rs1794957314","clinical_significance":[]},{"source":"dbSNP","start":140472458,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140472458,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs58647694"},{"start":140472461,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C","G"],"end":140472461,"strand":1,"feature_type":"variation","id":"rs913484538","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1291643506","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472468,"feature_type":"variation","strand":1,"end":140472468,"alleles":["A","G"]},{"id":"rs1457356378","seq_region_name":"7","clinical_significance":[],"start":140472469,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140472469,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794957798","source":"dbSNP","start":140472473,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140472473,"alleles":["T","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1389403912","source":"dbSNP","start":140472476,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140472476,"feature_type":"variation","strand":1},{"id":"rs2130347305","seq_region_name":"7","clinical_significance":[],"end":140472477,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140472477,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["T","C","G"],"end":140472482,"feature_type":"variation","strand":1,"source":"dbSNP","start":140472482,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130347320"},{"start":140472484,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140472484,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794957902","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140472485,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472485,"clinical_significance":[],"seq_region_name":"7","id":"rs1585492700"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1003991513","alleles":["T","C"],"end":140472487,"feature_type":"variation","strand":1,"source":"dbSNP","start":140472487,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140472489,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472489,"source":"dbSNP","seq_region_name":"7","id":"rs971073538","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472490,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140472490,"clinical_significance":[],"seq_region_name":"7","id":"rs565283560"},{"clinical_significance":[],"id":"rs1177244239","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140472492,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472492},{"start":140472493,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140472493,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs566143657","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140472513,"alleles":["GTTTTTGCATTGTGTTTTTGC","GTTTTTGC"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472493,"source":"dbSNP","seq_region_name":"7","id":"rs1435212100","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794958367","clinical_significance":[],"alleles":["T","C"],"end":140472498,"strand":1,"feature_type":"variation","start":140472498,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs763452160","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140472500,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472500},{"clinical_significance":[],"seq_region_name":"7","id":"rs879678328","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140472502,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472502},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472502,"feature_type":"variation","strand":1,"end":140472503,"alleles":["TT","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794958518"},{"end":140472505,"alleles":["T","-"],"strand":1,"feature_type":"variation","start":140472505,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1449618474","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794958581","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140472505,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472505,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140472508,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472508,"source":"dbSNP","seq_region_name":"7","id":"rs1191077889","clinical_significance":[]},{"alleles":["T","C"],"end":140472511,"feature_type":"variation","strand":1,"source":"dbSNP","start":140472511,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794958743"},{"seq_region_name":"7","id":"rs1012315473","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472513,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140472513},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794958804","source":"dbSNP","start":140472514,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140472514,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1248074546","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472515,"feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140472515},{"seq_region_name":"7","id":"rs1210107704","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472518,"source":"dbSNP","strand":1,"feature_type":"variation","end":140472518,"alleles":["T","C"]},{"end":140472519,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140472519,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1794958988","seq_region_name":"7"},{"alleles":["AG","-"],"end":140472520,"strand":1,"feature_type":"variation","start":140472519,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1189871514","clinical_significance":[]},{"seq_region_name":"7","id":"rs1259850822","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140472521,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472521,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1794959143","seq_region_name":"7","feature_type":"variation","strand":1,"end":140472524,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472524},{"alleles":["A","G"],"end":140472529,"feature_type":"variation","strand":1,"source":"dbSNP","start":140472529,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs927038211"},{"seq_region_name":"7","id":"rs1794959228","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140472531,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472531,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794959291","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472532,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140472532},{"seq_region_name":"7","id":"rs2130347636","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140472533,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472533,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1371287465","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472534,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140472534},{"seq_region_name":"7","id":"rs536385088","clinical_significance":[],"end":140472535,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140472535,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140472536,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140472536,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1017012193","clinical_significance":[]},{"end":140472537,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140472537,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1365889308","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs148449388","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140472538,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472538},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472540,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140472540,"seq_region_name":"7","id":"rs1794959897","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794959969","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140472541,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472541},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140472543,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472543,"source":"dbSNP","id":"rs919793176","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs929791848","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472545,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140472545},{"seq_region_name":"7","id":"rs1404140618","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472546,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140472546},{"source":"dbSNP","start":140472547,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140472547,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794960331"},{"clinical_significance":[],"id":"rs1047046926","seq_region_name":"7","source":"dbSNP","start":140472549,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140472549,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1335047287","source":"dbSNP","start":140472550,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140472550,"alleles":["G","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs891014192","clinical_significance":[],"start":140472551,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140472551,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140472552,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472552,"clinical_significance":[],"seq_region_name":"7","id":"rs1794960698"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472557,"feature_type":"variation","strand":1,"end":140472557,"alleles":["T","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1008903873"},{"end":140472559,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140472559,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1040372836","clinical_significance":[]},{"id":"rs1175847522","seq_region_name":"7","clinical_significance":[],"start":140472561,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140472561,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472562,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140472562,"seq_region_name":"7","id":"rs900595328","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140472569,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472569,"source":"dbSNP","id":"rs1435927429","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs996302154","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472574,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140472574},{"id":"rs1026357835","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472576,"source":"dbSNP","strand":1,"feature_type":"variation","end":140472576,"alleles":["G","C"]},{"seq_region_name":"7","id":"rs1297758095","clinical_significance":[],"strand":1,"feature_type":"variation","end":140472578,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472578,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472579,"feature_type":"variation","strand":1,"end":140472579,"alleles":["A","G"],"clinical_significance":[],"id":"rs1585492879","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794961570","source":"dbSNP","start":140472579,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AG","-"],"end":140472580,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130347945","alleles":["T","G"],"end":140472583,"feature_type":"variation","strand":1,"source":"dbSNP","start":140472583,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140472585,"alleles":["TTT","TT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472583,"source":"dbSNP","seq_region_name":"7","id":"rs1189934056","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472588,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140472588,"clinical_significance":[],"id":"rs1033494556","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794961686","end":140472589,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140472589,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140472590,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140472590,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1463109389"},{"end":140472591,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140472591,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1794961801","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs957601571","end":140472592,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140472592,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["T","A","C"],"end":140472593,"feature_type":"variation","strand":1,"source":"dbSNP","start":140472593,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794961931"},{"clinical_significance":[],"id":"rs1794961997","seq_region_name":"7","source":"dbSNP","start":140472593,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140472595,"alleles":["TTA","-"],"feature_type":"variation","strand":1},{"end":140472594,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140472594,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1010355197","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794962130","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140472596,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472596},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140472597,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472597,"clinical_significance":[],"seq_region_name":"7","id":"rs1794962190"},{"start":140472598,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140472598,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1484045882","clinical_significance":[]},{"source":"dbSNP","start":140472599,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140472599,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794962309"},{"seq_region_name":"7","id":"rs1020504024","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472600,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140472600},{"alleles":["C","A","T"],"end":140472607,"feature_type":"variation","strand":1,"source":"dbSNP","start":140472607,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794962403"},{"source":"dbSNP","start":140472609,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140472609,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs59212496"},{"seq_region_name":"7","id":"rs1794962525","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["CG","-"],"end":140472610,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472609,"source":"dbSNP"},{"end":140472610,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140472610,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs955613246"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472615,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140472615,"seq_region_name":"7","id":"rs1794962654","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1326171675","source":"dbSNP","start":140472616,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140472616,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140472618,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472618,"clinical_significance":[],"id":"rs1794962833","seq_region_name":"7"},{"alleles":["C","G","T"],"end":140472620,"strand":1,"feature_type":"variation","start":140472620,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs181806692","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs536476746","source":"dbSNP","start":140472621,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140472621,"alleles":["C","A"],"feature_type":"variation","strand":1},{"id":"rs61689769","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140472623,"alleles":["T","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472623,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794963095","alleles":["G","C"],"end":140472626,"feature_type":"variation","strand":1,"source":"dbSNP","start":140472626,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1794963135","clinical_significance":[],"strand":1,"feature_type":"variation","end":140472627,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472627,"source":"dbSNP"},{"source":"dbSNP","start":140472630,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140472630,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs943138517"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1465028424","feature_type":"variation","strand":1,"alleles":["T","TT"],"end":140472630,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472630},{"clinical_significance":[],"id":"rs2130348322","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472631,"feature_type":"variation","strand":1,"end":140472631,"alleles":["G","T"]},{"end":140472633,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140472633,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130348332","clinical_significance":[]},{"end":140472634,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140472634,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1585493007","seq_region_name":"7"},{"id":"rs1325883186","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140472635,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472635,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1585493016","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472636,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140472636},{"start":140472639,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140472639,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs60785888","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1259103286","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472640,"feature_type":"variation","strand":1,"end":140472640,"alleles":["G","A"]},{"clinical_significance":[],"id":"rs974486275","seq_region_name":"7","alleles":["T","C"],"end":140472655,"feature_type":"variation","strand":1,"source":"dbSNP","start":140472655,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472657,"feature_type":"variation","strand":1,"end":140472657,"alleles":["A","G"],"clinical_significance":[],"id":"rs201834129","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472658,"source":"dbSNP","strand":1,"feature_type":"variation","end":140472658,"alleles":["G","C"],"seq_region_name":"7","id":"rs567061693","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472659,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140472659,"id":"rs1167195549","seq_region_name":"7","clinical_significance":[]},{"end":140472660,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140472660,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1449416979"},{"end":140472661,"alleles":["T","A","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140472661,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1199561344","seq_region_name":"7"},{"source":"dbSNP","start":140472664,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140472664,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs185549849"},{"seq_region_name":"7","id":"rs1794964336","clinical_significance":[],"alleles":["G","A"],"end":140472666,"strand":1,"feature_type":"variation","start":140472666,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1425159335","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140472667,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472667,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140472668,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472668,"source":"dbSNP","id":"rs1253710606","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794968107","source":"dbSNP","start":140472669,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140472669,"alleles":["T","TT"],"feature_type":"variation","strand":1},{"end":140472670,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140472670,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1209716825","seq_region_name":"7","clinical_significance":[]},{"start":140472671,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140472671,"alleles":["A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1483228828","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472673,"feature_type":"variation","strand":1,"end":140472674,"alleles":["CC","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1479334352"},{"alleles":["C","T"],"end":140472674,"strand":1,"feature_type":"variation","start":140472674,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794968370","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1202896136","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472678,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140472678},{"seq_region_name":"7","id":"rs770070817","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140472679,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472679,"source":"dbSNP"},{"source":"dbSNP","start":140472680,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140472680,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs190398356"},{"end":140472682,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140472682,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1457933051","seq_region_name":"7"},{"source":"dbSNP","start":140472683,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140472683,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs943905275","seq_region_name":"7"},{"source":"dbSNP","start":140472684,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140472684,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794968768"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472685,"feature_type":"variation","strand":1,"end":140472685,"alleles":["G","T"],"clinical_significance":[],"id":"rs1040012261","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1382946730","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472691,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140472691},{"id":"rs1292828787","seq_region_name":"7","clinical_significance":[],"alleles":["T","A"],"end":140472692,"strand":1,"feature_type":"variation","start":140472692,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1794969032","seq_region_name":"7","feature_type":"variation","strand":1,"end":140472693,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472693},{"strand":1,"feature_type":"variation","end":140472696,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472696,"source":"dbSNP","id":"rs1410679318","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1352663206","clinical_significance":[],"end":140472697,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140472697,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs939255701","end":140472699,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140472699,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1794969311","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140472700,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472700,"source":"dbSNP"},{"seq_region_name":"7","id":"rs900522670","clinical_significance":[],"end":140472703,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140472703,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472705,"source":"dbSNP","strand":1,"feature_type":"variation","end":140472705,"alleles":["A","G"],"seq_region_name":"7","id":"rs1392138093","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794969442","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140472706,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472706,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1794969502","clinical_significance":[],"end":140472707,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140472707,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs996579395","feature_type":"variation","strand":1,"end":140472709,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472709},{"clinical_significance":[],"seq_region_name":"7","id":"rs1054581244","feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140472710,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472710},{"clinical_significance":[],"id":"rs893190661","seq_region_name":"7","alleles":["A","T"],"end":140472711,"feature_type":"variation","strand":1,"source":"dbSNP","start":140472711,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140472713,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472713,"clinical_significance":[],"seq_region_name":"7","id":"rs765805041"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472716,"feature_type":"variation","strand":1,"end":140472716,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794969828"},{"seq_region_name":"7","id":"rs1794969903","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472721,"source":"dbSNP","strand":1,"feature_type":"variation","end":140472721,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130348966","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472722,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140472722},{"seq_region_name":"7","id":"rs751011787","clinical_significance":[],"start":140472723,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140472723,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1794970120","seq_region_name":"7","feature_type":"variation","strand":1,"end":140472724,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472724},{"seq_region_name":"7","id":"rs1253671794","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472726,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140472726},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140472727,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472727,"source":"dbSNP","seq_region_name":"7","id":"rs1025779349","clinical_significance":[]},{"clinical_significance":[],"id":"rs1179810300","seq_region_name":"7","end":140472731,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140472731,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["T","G"],"end":140472732,"strand":1,"feature_type":"variation","start":140472732,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794970460","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140472734,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472734,"source":"dbSNP","seq_region_name":"7","id":"rs1794970513","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794970557","clinical_significance":[],"strand":1,"feature_type":"variation","end":140472737,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472737,"source":"dbSNP"},{"source":"dbSNP","start":140472739,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140472739,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1794970618","seq_region_name":"7"},{"end":140472746,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140472746,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1437150700","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140472747,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472747,"source":"dbSNP","seq_region_name":"7","id":"rs577574654","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140472751,"alleles":["A","AA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472751,"clinical_significance":[],"seq_region_name":"7","id":"rs1794970792"},{"source":"dbSNP","start":140472753,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140472753,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs907479393"},{"source":"dbSNP","start":140472755,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140472758,"alleles":["CTCT","CT"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs112120514","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472756,"feature_type":"variation","strand":1,"end":140472756,"alleles":["T","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794971119"},{"clinical_significance":[],"id":"rs1794971214","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472757,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140472757},{"alleles":["G","T"],"end":140472759,"strand":1,"feature_type":"variation","start":140472759,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1354264464","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1272648861","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140472760,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472760,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1229202161","source":"dbSNP","start":140472761,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140472761,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1240803807","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472764,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140472764},{"end":140472770,"alleles":["AAAAAAA","AAAAAAAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140472764,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794971699"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794971810","feature_type":"variation","strand":1,"end":140472769,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472769},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794971900","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472771,"feature_type":"variation","strand":1,"end":140472771,"alleles":["T","A","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1258563795","end":140472772,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140472772,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794972106","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472773,"feature_type":"variation","strand":1,"end":140472783,"alleles":["TAATAATAATA","TAATAATAATAATA"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472775,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140472775,"seq_region_name":"7","id":"rs1794972205","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472779,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140472779,"id":"rs180887107","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1332172128","seq_region_name":"7","feature_type":"variation","strand":1,"end":140472782,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472782},{"seq_region_name":"7","id":"rs1794972486","clinical_significance":[],"start":140472784,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140472784,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"id":"rs556994762","seq_region_name":"7","clinical_significance":[],"start":140472785,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140472785,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1794972544","seq_region_name":"7","end":140472790,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140472790,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472791,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140472791,"clinical_significance":[],"seq_region_name":"7","id":"rs1794972605"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1209841449","source":"dbSNP","start":140472792,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140472792,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472796,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140472796,"clinical_significance":[],"seq_region_name":"7","id":"rs185236041"},{"id":"rs1794972743","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140472802,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472802,"source":"dbSNP"},{"start":140472803,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140472803,"alleles":["T","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs61577108","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472807,"feature_type":"variation","strand":1,"alleles":["TAACT","T"],"end":140472811,"clinical_significance":[],"seq_region_name":"7","id":"rs1457423283"},{"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140472808,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472808,"source":"dbSNP","seq_region_name":"7","id":"rs1794973004","clinical_significance":[]},{"end":140472810,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140472810,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1794973060","seq_region_name":"7"},{"seq_region_name":"7","id":"rs561366522","clinical_significance":[],"alleles":["T","A","C"],"end":140472812,"strand":1,"feature_type":"variation","start":140472812,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472814,"feature_type":"variation","strand":1,"end":140472814,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs558580200"},{"seq_region_name":"7","id":"rs1198464672","clinical_significance":[],"alleles":["A","G"],"end":140472815,"strand":1,"feature_type":"variation","start":140472815,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140472816,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140472816,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs375635732","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140472819,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472819,"source":"dbSNP","seq_region_name":"7","id":"rs1473438345","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140472820,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472820,"clinical_significance":[],"id":"rs1794973471","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140472821,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472821,"source":"dbSNP","seq_region_name":"7","id":"rs1247079064","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472823,"source":"dbSNP","strand":1,"feature_type":"variation","end":140472823,"alleles":["A","T"],"seq_region_name":"7","id":"rs1794973582","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472824,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140472824,"clinical_significance":[],"id":"rs1794973638","seq_region_name":"7"},{"end":140472825,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140472825,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1554450027","clinical_significance":[]},{"end":140472826,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140472826,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1252418426"},{"source":"dbSNP","start":140472826,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AAAAAAAAA","AAAAAAAA","AAAAAAAAAA"],"end":140472834,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs915032228"},{"clinical_significance":[],"id":"rs951086032","seq_region_name":"7","end":140472829,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140472829,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140472831,"alleles":["A","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140472831,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585493373"},{"id":"rs1794973992","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472834,"source":"dbSNP","strand":1,"feature_type":"variation","end":140472834,"alleles":["A","C","G"]},{"strand":1,"feature_type":"variation","end":140472835,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472835,"source":"dbSNP","seq_region_name":"7","id":"rs1794974058","clinical_significance":[]},{"alleles":["C","T"],"end":140472838,"feature_type":"variation","strand":1,"source":"dbSNP","start":140472838,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794974115"},{"clinical_significance":[],"seq_region_name":"7","id":"rs978337266","source":"dbSNP","start":140472842,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140472842,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472843,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140472843,"clinical_significance":[],"seq_region_name":"7","id":"rs982622657"},{"strand":1,"feature_type":"variation","end":140472844,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472844,"source":"dbSNP","seq_region_name":"7","id":"rs912427590","clinical_significance":[]},{"start":140472845,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140472845,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1277007668","clinical_significance":[]},{"id":"rs377151535","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140472846,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472846,"source":"dbSNP"},{"source":"dbSNP","start":140472850,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140472850,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs943833286"},{"seq_region_name":"7","id":"rs1794974486","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472851,"source":"dbSNP","strand":1,"feature_type":"variation","end":140472851,"alleles":["C","T"]},{"end":140472852,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140472852,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1794974538","seq_region_name":"7"},{"id":"rs1163860702","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472853,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140472853},{"feature_type":"variation","strand":1,"alleles":["CACAC","CACACAC"],"end":140472857,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472853,"clinical_significance":[],"seq_region_name":"7","id":"rs1370976905"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472855,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140472855,"clinical_significance":[],"seq_region_name":"7","id":"rs975396812"},{"seq_region_name":"7","id":"rs1794974792","clinical_significance":[],"strand":1,"feature_type":"variation","end":140472856,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472856,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140472857,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472857,"source":"dbSNP","seq_region_name":"7","id":"rs1794974856","clinical_significance":[]},{"source":"dbSNP","start":140472858,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140472858,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794974928"},{"seq_region_name":"7","id":"rs573328515","clinical_significance":[],"start":140472859,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140472859,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472860,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140472860,"seq_region_name":"7","id":"rs540740633","clinical_significance":[]},{"end":140472862,"alleles":["TA","-"],"strand":1,"feature_type":"variation","start":140472861,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794975392","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472865,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140472865,"clinical_significance":[],"seq_region_name":"7","id":"rs1425555157"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472869,"source":"dbSNP","strand":1,"feature_type":"variation","end":140472869,"alleles":["G","A"],"seq_region_name":"7","id":"rs1794975475","clinical_significance":[]},{"id":"rs113482098","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472872,"source":"dbSNP","strand":1,"feature_type":"variation","end":140472872,"alleles":["C","A"]},{"seq_region_name":"7","id":"rs1794975699","clinical_significance":[],"end":140472875,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140472875,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472877,"source":"dbSNP","strand":1,"feature_type":"variation","end":140472877,"alleles":["G","A"],"id":"rs1794975804","seq_region_name":"7","clinical_significance":[]},{"end":140472878,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140472878,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794975898"},{"seq_region_name":"7","id":"rs893241300","clinical_significance":[],"alleles":["G","A"],"end":140472880,"strand":1,"feature_type":"variation","start":140472880,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1038342307","alleles":["G","C"],"end":140472881,"feature_type":"variation","strand":1,"source":"dbSNP","start":140472881,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1394460391","seq_region_name":"7","clinical_significance":[],"start":140472882,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["CC","C"],"end":140472883,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140472883,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472883,"source":"dbSNP","id":"rs1189288015","seq_region_name":"7","clinical_significance":[]},{"id":"rs755243872","seq_region_name":"7","clinical_significance":[],"alleles":["A","G"],"end":140472884,"strand":1,"feature_type":"variation","start":140472884,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1585493494","clinical_significance":[],"end":140472888,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140472888,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs369500621","feature_type":"variation","strand":1,"end":140472889,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472889},{"alleles":["A","G"],"end":140472891,"strand":1,"feature_type":"variation","start":140472891,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1240440434","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472893,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140472893,"seq_region_name":"7","id":"rs1393494356","clinical_significance":[]},{"alleles":["A","T"],"end":140472895,"feature_type":"variation","strand":1,"source":"dbSNP","start":140472895,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs2130350087","seq_region_name":"7"},{"seq_region_name":"7","id":"rs150568542","clinical_significance":[],"strand":1,"feature_type":"variation","end":140472896,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472896,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1794976761","clinical_significance":[],"alleles":["C","T"],"end":140472899,"strand":1,"feature_type":"variation","start":140472899,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140472900,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472900,"source":"dbSNP","id":"rs1281146815","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1041772171","clinical_significance":[],"start":140472902,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140472902,"strand":1,"feature_type":"variation"},{"start":140472903,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140472903,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs2130350135","seq_region_name":"7","clinical_significance":[]},{"id":"rs190050080","seq_region_name":"7","clinical_significance":[],"end":140472905,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140472905,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["A","C"],"end":140472906,"feature_type":"variation","strand":1,"source":"dbSNP","start":140472906,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1047694034"},{"alleles":["A","T"],"end":140472909,"feature_type":"variation","strand":1,"source":"dbSNP","start":140472909,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794977083"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1244916452","alleles":["G","A"],"end":140472910,"feature_type":"variation","strand":1,"source":"dbSNP","start":140472910,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs563074596","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472911,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140472911},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472914,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140472914,"clinical_significance":[],"seq_region_name":"7","id":"rs1794977258"},{"seq_region_name":"7","id":"rs1231276196","clinical_significance":[],"end":140472916,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140472916,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472917,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140472917,"seq_region_name":"7","id":"rs1794977376","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1036562840","alleles":["C","A","T"],"end":140472922,"feature_type":"variation","strand":1,"source":"dbSNP","start":140472922,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs891315102","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472923,"source":"dbSNP","strand":1,"feature_type":"variation","end":140472923,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794977573","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472926,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140472926},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472927,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140472927,"clinical_significance":[],"seq_region_name":"7","id":"rs1794977640"},{"feature_type":"variation","strand":1,"end":140472930,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472930,"clinical_significance":[],"seq_region_name":"7","id":"rs1794977695"},{"clinical_significance":[],"id":"rs530302652","seq_region_name":"7","source":"dbSNP","start":140472931,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140472931,"alleles":["T","C"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140472933,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140472933,"alleles":["T","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs548419363"},{"clinical_significance":[],"seq_region_name":"7","id":"rs566723148","source":"dbSNP","start":140472934,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140472934,"alleles":["G","A"],"feature_type":"variation","strand":1},{"alleles":["G","A"],"end":140472935,"strand":1,"feature_type":"variation","start":140472935,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130350334","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140472936,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472936,"clinical_significance":[],"seq_region_name":"7","id":"rs577041093"},{"alleles":["AAA","AAAA"],"end":140472940,"feature_type":"variation","strand":1,"source":"dbSNP","start":140472938,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1432697113"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1374628763","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472941,"feature_type":"variation","strand":1,"end":140472941,"alleles":["C","A"]},{"clinical_significance":[],"id":"rs964260232","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472943,"feature_type":"variation","strand":1,"end":140472943,"alleles":["C","T"]},{"source":"dbSNP","start":140472944,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140472944,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794978228"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140472945,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472945,"clinical_significance":[],"seq_region_name":"7","id":"rs1356609848"},{"feature_type":"variation","strand":1,"end":140472947,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472947,"clinical_significance":[],"seq_region_name":"7","id":"rs1794978430"},{"seq_region_name":"7","id":"rs1034613863","clinical_significance":[],"start":140472956,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140472956,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs386718465","seq_region_name":"7","source":"dbSNP","start":140472956,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AAG","CAA"],"end":140472958,"feature_type":"variation","strand":1},{"end":140472958,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140472958,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs894679487","clinical_significance":[]},{"id":"rs181295699","seq_region_name":"7","clinical_significance":[],"start":140472959,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140472959,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"end":140472967,"alleles":["AAAAAA","AAAAA"],"strand":1,"feature_type":"variation","start":140472962,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1563096030","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472963,"feature_type":"variation","strand":1,"end":140472963,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs56006349"},{"seq_region_name":"7","id":"rs1027035171","clinical_significance":[],"alleles":["A","C","G"],"end":140472965,"strand":1,"feature_type":"variation","start":140472965,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140472968,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472968,"clinical_significance":[],"seq_region_name":"7","id":"rs1794979017"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472970,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140472970,"id":"rs968221862","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1175201073","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472973,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140472973},{"start":140472974,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140472974,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1248704241","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140472978,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472978,"source":"dbSNP","seq_region_name":"7","id":"rs1794979295","clinical_significance":[]},{"seq_region_name":"7","id":"rs1418681785","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472981,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140472981},{"seq_region_name":"7","id":"rs1794979458","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472982,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140472982},{"clinical_significance":[],"id":"rs977893562","seq_region_name":"7","feature_type":"variation","strand":1,"end":140472983,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472983},{"seq_region_name":"7","id":"rs1794979582","clinical_significance":[],"start":140472985,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140472985,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140472990,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472990,"source":"dbSNP","id":"rs1794979658","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794979712","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140472990,"source":"dbSNP","strand":1,"feature_type":"variation","end":140473027,"alleles":["ACCTGTAATCCCAACTACTCGGGAGGCTGAGGCAGGGA","A"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472992,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140472992,"clinical_significance":[],"seq_region_name":"7","id":"rs1794979768"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794979839","feature_type":"variation","strand":1,"end":140472998,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140472998},{"strand":1,"feature_type":"variation","end":140473003,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473003,"source":"dbSNP","seq_region_name":"7","id":"rs1275828848","clinical_significance":[]},{"seq_region_name":"7","id":"rs1207867381","clinical_significance":[],"start":140473004,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140473004,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1306306747","clinical_significance":[],"end":140473007,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140473007,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140473009,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473009,"source":"dbSNP","seq_region_name":"7","id":"rs923673039","clinical_significance":[]},{"id":"rs756227431","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140473010,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473010,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1379434900","source":"dbSNP","start":140473011,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140473011,"alleles":["G","A","C"],"feature_type":"variation","strand":1},{"start":140473015,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140473015,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs991992972","clinical_significance":[]},{"seq_region_name":"7","id":"rs1387214423","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140473016,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473016,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585493766","alleles":["A","G"],"end":140473019,"feature_type":"variation","strand":1,"source":"dbSNP","start":140473019,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs982550671","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473020,"source":"dbSNP","strand":1,"feature_type":"variation","end":140473020,"alleles":["G","A","C"]},{"feature_type":"variation","strand":1,"end":140473028,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473028,"clinical_significance":[],"seq_region_name":"7","id":"rs1354529528"},{"clinical_significance":[],"id":"rs1563096064","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["GCAGTGAGC","GC"],"end":140473038,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473030},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473031,"feature_type":"variation","strand":1,"end":140473031,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1308453868"},{"strand":1,"feature_type":"variation","end":140473034,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473034,"source":"dbSNP","id":"rs1794980949","seq_region_name":"7","clinical_significance":[]},{"id":"rs1431530009","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473036,"source":"dbSNP","strand":1,"feature_type":"variation","end":140473036,"alleles":["A","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794981048","end":140473037,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140473037,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140473039,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473039,"source":"dbSNP","id":"rs1422807180","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs185569644","seq_region_name":"7","end":140473040,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140473040,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140473041,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140473041,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1405961037","seq_region_name":"7"},{"clinical_significance":[],"id":"rs947919920","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473042,"feature_type":"variation","strand":1,"end":140473042,"alleles":["G","A"]},{"source":"dbSNP","start":140473045,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140473045,"alleles":["C","A","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs974084936"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473046,"source":"dbSNP","strand":1,"feature_type":"variation","end":140473046,"alleles":["G","A"],"id":"rs1794981444","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794981489","clinical_significance":[],"start":140473050,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140473050,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"end":140473051,"alleles":["CA","-"],"strand":1,"feature_type":"variation","start":140473050,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794981536","clinical_significance":[]},{"end":140473052,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140473052,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs60137728","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473053,"source":"dbSNP","strand":1,"feature_type":"variation","end":140473053,"alleles":["T","C","G"],"seq_region_name":"7","id":"rs1794981702","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140473054,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473054,"clinical_significance":[],"id":"rs1184846684","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794981821","end":140473056,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140473056,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473057,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140473057,"seq_region_name":"7","id":"rs975619670","clinical_significance":[]},{"start":140473058,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140473058,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs921196094","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473059,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","-"],"end":140473059,"seq_region_name":"7","id":"rs1794982035","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140473061,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473061,"source":"dbSNP","seq_region_name":"7","id":"rs2130351065","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473063,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140473063,"seq_region_name":"7","id":"rs191707654","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs990179423","source":"dbSNP","start":140473064,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140473064,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794982262","source":"dbSNP","start":140473065,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140473065,"feature_type":"variation","strand":1},{"alleles":["T","C"],"end":140473066,"feature_type":"variation","strand":1,"source":"dbSNP","start":140473066,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794982321"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473067,"source":"dbSNP","strand":1,"feature_type":"variation","end":140473067,"alleles":["C","T"],"id":"rs1274527020","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","G"],"end":140473071,"strand":1,"feature_type":"variation","start":140473071,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130351137","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1372199788","source":"dbSNP","start":140473075,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140473075,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473075,"feature_type":"variation","strand":1,"end":140473077,"alleles":["GAC","-"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794982516"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473076,"feature_type":"variation","strand":1,"end":140473081,"alleles":["ACAACA","ACA"],"clinical_significance":[],"seq_region_name":"7","id":"rs1333768679"},{"seq_region_name":"7","id":"rs1794982632","clinical_significance":[],"start":140473079,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140473081,"alleles":["ACA","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs914605303","seq_region_name":"7","source":"dbSNP","start":140473080,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140473080,"alleles":["C","G","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1288737917","source":"dbSNP","start":140473081,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AGAGAGA","AGAGA"],"end":140473087,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1411506961","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140473082,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473082},{"seq_region_name":"7","id":"rs946033425","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473084,"source":"dbSNP","strand":1,"feature_type":"variation","end":140473084,"alleles":["G","A","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs745865464","end":140473088,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140473088,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140473090,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["CC","C"],"end":140473091,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794982968"},{"seq_region_name":"7","id":"rs907261815","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473091,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140473091},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794983086","source":"dbSNP","start":140473095,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140473095,"alleles":["T","A"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473097,"feature_type":"variation","strand":1,"end":140473101,"alleles":["AAAAA","AAAA"],"clinical_significance":[],"seq_region_name":"7","id":"rs1563096110"},{"clinical_significance":[],"seq_region_name":"7","id":"rs559356136","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473097,"feature_type":"variation","strand":1,"end":140473125,"alleles":["AAAAAGAAAAAGAAAAAGAAAAAGAAAAA","AAAAAGAAAAAGAAAAA","AAAAAGAAAAAGAAAAAGAAAAA","AAAAAGAAAAAGAAAAAGAAAAAGAAAAAGAAAAA","AAAAAGAAAAAGAAAAAGAAAAAGAAAAAGAAAAAGAAAAA"]},{"id":"rs1461095980","seq_region_name":"7","clinical_significance":[],"alleles":["A","G"],"end":140473101,"strand":1,"feature_type":"variation","start":140473101,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140473102,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C"],"end":140473102,"strand":1,"feature_type":"variation","id":"rs1413049473","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140473103,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140473103,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585493931"},{"strand":1,"feature_type":"variation","end":140473104,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473104,"source":"dbSNP","seq_region_name":"7","id":"rs1794983542","clinical_significance":[]},{"end":140473110,"alleles":["AAGAA","AA"],"strand":1,"feature_type":"variation","start":140473106,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1380013802","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795823951","source":"dbSNP","start":140473107,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140473107,"alleles":["A","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1417629786","clinical_significance":[],"alleles":["G","A","T"],"end":140473108,"strand":1,"feature_type":"variation","start":140473108,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473108,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","-"],"end":140473108,"seq_region_name":"7","id":"rs1794983715","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140473110,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473110,"clinical_significance":[],"seq_region_name":"7","id":"rs1039808117"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473110,"source":"dbSNP","strand":1,"feature_type":"variation","end":140473114,"alleles":["AAAAG","AAAAGTAAAAG"],"seq_region_name":"7","id":"rs1192229302","clinical_significance":[]},{"source":"dbSNP","start":140473111,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AAAGAAA","AAA"],"end":140473117,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1244598812","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1275270761","end":140473114,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140473114,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["A","C","G"],"end":140473116,"strand":1,"feature_type":"variation","start":140473116,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1563096127","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794984110","alleles":["A","G"],"end":140473119,"feature_type":"variation","strand":1,"source":"dbSNP","start":140473119,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1309126768","source":"dbSNP","start":140473120,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140473120,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140473121,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473121,"clinical_significance":[],"id":"rs1794984228","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473122,"source":"dbSNP","strand":1,"feature_type":"variation","end":140473122,"alleles":["A","G"],"seq_region_name":"7","id":"rs1794984283","clinical_significance":[]},{"end":140473130,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140473130,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs116030971"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1056343627","end":140473132,"alleles":["T","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140473132,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140473135,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140473135,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs894737907","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140473136,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473136,"clinical_significance":[],"id":"rs574470350","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1306064580","clinical_significance":[],"alleles":["C","T"],"end":140473139,"strand":1,"feature_type":"variation","start":140473139,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["G","A"],"end":140473140,"strand":1,"feature_type":"variation","start":140473140,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1048657712","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794984670","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473142,"source":"dbSNP","strand":1,"feature_type":"variation","end":140473142,"alleles":["C","A"]},{"end":140473143,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140473143,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1373160317"},{"alleles":["G","T"],"end":140473146,"strand":1,"feature_type":"variation","start":140473146,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1204612483","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473147,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140473147,"seq_region_name":"7","id":"rs886811164","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473148,"feature_type":"variation","strand":1,"alleles":["ATTTCTCCTCCAAACA","A"],"end":140473163,"clinical_significance":[],"seq_region_name":"7","id":"rs1794984898"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140473149,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473149,"clinical_significance":[],"seq_region_name":"7","id":"rs1794984964"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794985018","source":"dbSNP","start":140473152,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140473152,"alleles":["C","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs2130351667","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140473153,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473153,"source":"dbSNP"},{"seq_region_name":"7","id":"rs2130351682","clinical_significance":[],"end":140473154,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140473154,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1442858226","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473155,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140473155},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473156,"feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140473156,"clinical_significance":[],"seq_region_name":"7","id":"rs1389468686"},{"feature_type":"variation","strand":1,"end":140473158,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473158,"clinical_significance":[],"id":"rs1322736847","seq_region_name":"7"},{"id":"rs1451921261","seq_region_name":"7","clinical_significance":[],"end":140473162,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140473162,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794985366","alleles":["C","T"],"end":140473168,"feature_type":"variation","strand":1,"source":"dbSNP","start":140473168,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473169,"feature_type":"variation","strand":1,"end":140473169,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1182997484"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794985479","alleles":["T","C"],"end":140473172,"feature_type":"variation","strand":1,"source":"dbSNP","start":140473172,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473175,"feature_type":"variation","strand":1,"end":140473175,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1794985529"},{"source":"dbSNP","start":140473176,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140473176,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1003875784"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473176,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TATAAGTATA","TATA"],"end":140473185,"seq_region_name":"7","id":"rs903548206","clinical_significance":[]},{"source":"dbSNP","start":140473177,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140473177,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs554764279","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794985778","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473178,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140473178},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794985833","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473181,"feature_type":"variation","strand":1,"end":140473181,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794985881","alleles":["A","G"],"end":140473183,"feature_type":"variation","strand":1,"source":"dbSNP","start":140473183,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794985941","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473184,"feature_type":"variation","strand":1,"end":140473184,"alleles":["T","C"]},{"alleles":["A","G"],"end":140473185,"feature_type":"variation","strand":1,"source":"dbSNP","start":140473185,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1794985994"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794986054","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140473186,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473186},{"id":"rs1794986113","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140473189,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473189,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1030790055","clinical_significance":[],"alleles":["T","G"],"end":140473190,"strand":1,"feature_type":"variation","start":140473190,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["T","C"],"end":140473191,"strand":1,"feature_type":"variation","start":140473191,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794986230","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140473192,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473192,"clinical_significance":[],"seq_region_name":"7","id":"rs2130351923"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473200,"feature_type":"variation","strand":1,"alleles":["ATGAT","AT"],"end":140473204,"clinical_significance":[],"id":"rs1332483384","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs997884464","feature_type":"variation","strand":1,"end":140473201,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473201},{"seq_region_name":"7","id":"rs2130351959","clinical_significance":[],"start":140473205,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140473205,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["ACCACCA","ACCA"],"end":140473211,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473205,"source":"dbSNP","id":"rs1794986404","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140473207,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473207,"source":"dbSNP","seq_region_name":"7","id":"rs573092635","clinical_significance":[]},{"id":"rs35197255","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140473208,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473208,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140473208,"alleles":["A","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473208,"source":"dbSNP","id":"rs1794986610","seq_region_name":"7","clinical_significance":[]},{"end":140473209,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140473209,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1195412780"},{"start":140473209,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140473210,"alleles":["CC","-"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1238658292","clinical_significance":[]},{"alleles":["-","A"],"end":140473209,"strand":1,"feature_type":"variation","start":140473210,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794986782","clinical_significance":[]},{"start":140473210,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140473210,"alleles":["C","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1453207522","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794986902","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473211,"source":"dbSNP","strand":1,"feature_type":"variation","end":140473211,"alleles":["A","C"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473211,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AAAAAAAAAAAAAAAAA","AAAAAAAAAAAA","AAAAAAAAAAAAAA","AAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAA"],"end":140473227,"seq_region_name":"7","id":"rs534529617","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140473212,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473212,"source":"dbSNP","seq_region_name":"7","id":"rs1395232763","clinical_significance":[]},{"seq_region_name":"7","id":"rs1306425261","clinical_significance":[],"start":140473218,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["-","G"],"end":140473217,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1297853841","clinical_significance":[],"strand":1,"feature_type":"variation","end":140473220,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473220,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140473221,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473221,"clinical_significance":[],"seq_region_name":"7","id":"rs960699034"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473223,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["-","C"],"end":140473222,"id":"rs1794987738","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1563096190","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473223,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140473223},{"clinical_significance":[],"id":"rs1794987911","seq_region_name":"7","source":"dbSNP","start":140473224,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["-","C"],"end":140473223,"feature_type":"variation","strand":1},{"end":140473224,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140473224,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794987964","clinical_significance":[]},{"source":"dbSNP","start":140473224,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140473227,"alleles":["AAAA","AAAAAACAAAA"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1563096194"},{"feature_type":"variation","strand":1,"end":140473225,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473225,"clinical_significance":[],"seq_region_name":"7","id":"rs77927799"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563096199","source":"dbSNP","start":140473226,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140473226,"feature_type":"variation","strand":1},{"id":"rs1794988237","seq_region_name":"7","clinical_significance":[],"start":140473226,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","ACA"],"end":140473226,"strand":1,"feature_type":"variation"},{"end":140473229,"alleles":["AACA","A"],"strand":1,"feature_type":"variation","start":140473226,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1352421313","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794988366","clinical_significance":[],"strand":1,"feature_type":"variation","end":140473226,"alleles":["-","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473227,"source":"dbSNP"},{"source":"dbSNP","start":140473227,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140473227,"alleles":["A","C","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs183457410"},{"id":"rs1465083146","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["ACA","A","ACACA"],"end":140473229,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473227,"source":"dbSNP"},{"start":140473228,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","CC"],"end":140473228,"strand":1,"feature_type":"variation","id":"rs58539466","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs369293522","clinical_significance":[],"end":140473228,"alleles":["C","-"],"strand":1,"feature_type":"variation","start":140473228,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs775959791","feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140473228,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473228},{"start":140473228,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140473234,"alleles":["CATCATC","CATC"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794988785","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140473230,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473230,"source":"dbSNP","id":"rs749694506","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140473230,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140473231,"alleles":["TC","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1291504745","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473231,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140473231,"clinical_significance":[],"seq_region_name":"7","id":"rs768929967"},{"feature_type":"variation","strand":1,"end":140473232,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473232,"clinical_significance":[],"seq_region_name":"7","id":"rs1443825043"},{"start":140473233,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140473233,"alleles":["T","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130352437","clinical_significance":[]},{"seq_region_name":"7","id":"rs1794989087","clinical_significance":[],"start":140473234,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140473234,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"id":"rs1794989155","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473235,"source":"dbSNP","strand":1,"feature_type":"variation","end":140473235,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs774409593","end":140473236,"alleles":["CA","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140473235,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1304799010","seq_region_name":"7","clinical_significance":[],"start":140473237,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140473237,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"end":140473242,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140473242,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1330636673"},{"start":140473243,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140473243,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs1194756096","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140473245,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473245,"clinical_significance":[],"seq_region_name":"7","id":"rs188857707"},{"id":"rs1260685540","seq_region_name":"7","clinical_significance":[],"alleles":["AA","AAA"],"end":140473248,"strand":1,"feature_type":"variation","start":140473247,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140473249,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140473249,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1182090233"},{"seq_region_name":"7","id":"rs1238595789","clinical_significance":[],"alleles":["G","C"],"end":140473252,"strand":1,"feature_type":"variation","start":140473252,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140473255,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473255,"clinical_significance":[],"seq_region_name":"7","id":"rs965463899"},{"start":140473256,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140473256,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","id":"rs1176756256","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1023445799","source":"dbSNP","start":140473259,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140473259,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1473127947","clinical_significance":[],"alleles":["C","T"],"end":140473260,"strand":1,"feature_type":"variation","start":140473260,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140473263,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140473263,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs996712891"},{"clinical_significance":[],"seq_region_name":"7","id":"rs762149845","end":140473264,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140473264,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1585494368","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140473266,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473266},{"end":140473275,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140473275,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1563096250"},{"feature_type":"variation","strand":1,"end":140473277,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473277,"clinical_significance":[],"id":"rs1342830059","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794990305","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473278,"feature_type":"variation","strand":1,"end":140473278,"alleles":["C","A"]},{"feature_type":"variation","strand":1,"end":140473280,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473280,"clinical_significance":[],"id":"rs140562693","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1171790454","clinical_significance":[],"start":140473281,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140473281,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs767469268","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473282,"feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140473282},{"clinical_significance":[],"seq_region_name":"7","id":"rs748176263","source":"dbSNP","start":140473283,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140473289,"alleles":["TATTATT","TATT"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140473284,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140473284,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794990605"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140473294,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473294,"clinical_significance":[],"seq_region_name":"7","id":"rs989828664"},{"source":"dbSNP","start":140473297,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140473297,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1794990658","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140473298,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473298,"source":"dbSNP","seq_region_name":"7","id":"rs773380874","clinical_significance":[]},{"alleles":["C","G"],"end":140473299,"feature_type":"variation","strand":1,"source":"dbSNP","start":140473299,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs930025541","seq_region_name":"7"},{"id":"rs17161569","seq_region_name":"7","clinical_significance":[],"start":140473302,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140473302,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs765180570","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473305,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140473305},{"alleles":["T","C","G"],"end":140473307,"feature_type":"variation","strand":1,"source":"dbSNP","start":140473307,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs563191919"},{"source":"dbSNP","start":140473310,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140473310,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1448056885","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1285473283","source":"dbSNP","start":140473312,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140473314,"alleles":["AGA","A"],"feature_type":"variation","strand":1},{"end":140473318,"alleles":["CTCT","CT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140473315,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1215533077"},{"seq_region_name":"7","id":"rs1353773918","clinical_significance":[],"strand":1,"feature_type":"variation","end":140473316,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473316,"source":"dbSNP"},{"id":"rs1794991389","seq_region_name":"7","clinical_significance":[],"end":140473318,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140473318,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140473322,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140473322,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1794991452","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1253522585","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473323,"feature_type":"variation","strand":1,"end":140473323,"alleles":["C","A","T"]},{"seq_region_name":"7","id":"rs1399328041","clinical_significance":[],"end":140473326,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140473326,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs200135272","clinical_significance":[],"start":140473327,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C"],"end":140473327,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473332,"source":"dbSNP","strand":1,"feature_type":"variation","end":140473332,"alleles":["A","G"],"seq_region_name":"7","id":"rs977352554","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473333,"source":"dbSNP","strand":1,"feature_type":"variation","end":140473333,"alleles":["C","T"],"seq_region_name":"7","id":"rs1794991769","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140473337,"alleles":["TGTG","TG"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473334,"clinical_significance":[],"id":"rs944090982","seq_region_name":"7"},{"end":140473338,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140473338,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs928741666","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473339,"feature_type":"variation","strand":1,"end":140473339,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130352994"},{"seq_region_name":"7","id":"rs1476001160","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473341,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140473341},{"end":140473342,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140473342,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1480971454","seq_region_name":"7"},{"alleles":["AAAA","AA","AAA"],"end":140473345,"strand":1,"feature_type":"variation","start":140473342,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1039860781","clinical_significance":[]},{"start":140473343,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140473343,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs530279708","clinical_significance":[]},{"clinical_significance":[],"id":"rs1794992248","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473347,"feature_type":"variation","strand":1,"alleles":["ACA","A"],"end":140473349},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140473348,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473348,"source":"dbSNP","id":"rs1252499825","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473357,"source":"dbSNP","strand":1,"feature_type":"variation","end":140473358,"alleles":["CT","CTCT"],"seq_region_name":"7","id":"rs1194018226","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140473360,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473360,"clinical_significance":[],"id":"rs1055868097","seq_region_name":"7"},{"alleles":["A","C"],"end":140473362,"feature_type":"variation","strand":1,"source":"dbSNP","start":140473362,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585494537"},{"alleles":["C","T"],"end":140473366,"feature_type":"variation","strand":1,"source":"dbSNP","start":140473366,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1426798957","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473370,"feature_type":"variation","strand":1,"end":140473370,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs79453306"},{"seq_region_name":"7","id":"rs931495371","clinical_significance":[],"start":140473374,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140473374,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1235337716","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473375,"source":"dbSNP","strand":1,"feature_type":"variation","end":140473375,"alleles":["T","G"]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140473376,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473376,"clinical_significance":[],"seq_region_name":"7","id":"rs1794992834"},{"seq_region_name":"7","id":"rs1794992883","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473377,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140473377},{"clinical_significance":[],"seq_region_name":"7","id":"rs1333031615","alleles":["C","T"],"end":140473379,"feature_type":"variation","strand":1,"source":"dbSNP","start":140473379,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140473392,"alleles":["CTTAGAAACCT","CTTAGAAACCTTAGAAACCT"],"strand":1,"feature_type":"variation","start":140473382,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585494570","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140473384,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473384,"source":"dbSNP","seq_region_name":"7","id":"rs1048708867","clinical_significance":[]},{"start":140473385,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","AA"],"end":140473385,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794993095","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473393,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140473393,"clinical_significance":[],"id":"rs1794993156","seq_region_name":"7"},{"start":140473395,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140473395,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs947546505","clinical_significance":[]},{"alleles":["G","A"],"end":140473399,"feature_type":"variation","strand":1,"source":"dbSNP","start":140473399,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1794993269","seq_region_name":"7"},{"end":140473400,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140473400,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794993327","clinical_significance":[]},{"seq_region_name":"7","id":"rs1563096307","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473401,"source":"dbSNP","strand":1,"feature_type":"variation","end":140473401,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1794993421","clinical_significance":[],"start":140473402,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140473402,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs144527441","alleles":["A","T"],"end":140473407,"feature_type":"variation","strand":1,"source":"dbSNP","start":140473407,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1794993534","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473408,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140473408},{"end":140473410,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140473410,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1410895899"},{"seq_region_name":"7","id":"rs1337902712","clinical_significance":[],"strand":1,"feature_type":"variation","end":140473415,"alleles":["AGAGA","AGA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473411,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1327366554","clinical_significance":[],"alleles":["G","A"],"end":140473412,"strand":1,"feature_type":"variation","start":140473412,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140473413,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473413,"source":"dbSNP","seq_region_name":"7","id":"rs887324834","clinical_significance":[]},{"source":"dbSNP","start":140473414,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140473414,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794993782"},{"id":"rs1003885738","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473415,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","T"],"end":140473415},{"alleles":["C","T"],"end":140473417,"strand":1,"feature_type":"variation","start":140473417,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1040712362","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140473418,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473418,"clinical_significance":[],"seq_region_name":"7","id":"rs1165062498"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473420,"feature_type":"variation","strand":1,"end":140473420,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs147874404"},{"source":"dbSNP","start":140473427,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140473427,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs764895891","seq_region_name":"7"},{"clinical_significance":[],"id":"rs112863893","seq_region_name":"7","source":"dbSNP","start":140473431,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140473431,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1794994278","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140473432,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473432,"source":"dbSNP"},{"source":"dbSNP","start":140473434,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140473434,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130353420"},{"alleles":["C","T"],"end":140473435,"strand":1,"feature_type":"variation","start":140473435,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1794994339","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140473437,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473437,"clinical_significance":[],"seq_region_name":"7","id":"rs1028055449"},{"seq_region_name":"7","id":"rs1428033620","clinical_significance":[],"start":140473437,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["CT","CTACT"],"end":140473438,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1288218232","feature_type":"variation","strand":1,"end":140473438,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473438},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794994507","source":"dbSNP","start":140473439,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140473439,"alleles":["G","GG"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473441,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140473441,"clinical_significance":[],"seq_region_name":"7","id":"rs1794994594"},{"id":"rs958151892","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473443,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140473443},{"feature_type":"variation","strand":1,"end":140473445,"alleles":["GGG","GG"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473443,"clinical_significance":[],"seq_region_name":"7","id":"rs554770337"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1470357547","source":"dbSNP","start":140473445,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140473445,"alleles":["G","T"],"feature_type":"variation","strand":1},{"start":140473447,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140473447,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794994947","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140473448,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473448,"source":"dbSNP","seq_region_name":"7","id":"rs1794995042","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1368139839","feature_type":"variation","strand":1,"end":140473450,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473450},{"clinical_significance":[],"seq_region_name":"7","id":"rs1225137237","feature_type":"variation","strand":1,"end":140473451,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473451},{"alleles":["A","G"],"end":140473452,"strand":1,"feature_type":"variation","start":140473452,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1365347376","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140473453,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473453,"clinical_significance":[],"seq_region_name":"7","id":"rs1179528119"},{"id":"rs1437211885","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473456,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140473456},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473471,"source":"dbSNP","strand":1,"feature_type":"variation","end":140473471,"alleles":["A","G"],"seq_region_name":"7","id":"rs1794995535","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140473474,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473474,"source":"dbSNP","id":"rs1794995629","seq_region_name":"7","clinical_significance":[]},{"start":140473477,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140473477,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794995696","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794995753","alleles":["C","G"],"end":140473478,"feature_type":"variation","strand":1,"source":"dbSNP","start":140473478,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140473481,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140473481,"alleles":["T","C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1215700307","clinical_significance":[]},{"end":140473483,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140473483,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1794995867","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1467306617","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473484,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140473484},{"clinical_significance":[],"seq_region_name":"7","id":"rs571287773","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140473485,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473485},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794996034","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473487,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140473487},{"seq_region_name":"7","id":"rs1794996083","clinical_significance":[],"start":140473491,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140473491,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140473496,"alleles":["AACAAC","AAC"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473491,"source":"dbSNP","id":"rs1229254850","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794996207","feature_type":"variation","strand":1,"end":140473494,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473494},{"seq_region_name":"7","id":"rs1353221922","clinical_significance":[],"start":140473496,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140473496,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140473498,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473498,"source":"dbSNP","seq_region_name":"7","id":"rs1794996339","clinical_significance":[]},{"source":"dbSNP","start":140473502,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140473502,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794996403"},{"seq_region_name":"7","id":"rs1794996464","clinical_significance":[],"end":140473503,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140473503,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1794996523","seq_region_name":"7","source":"dbSNP","start":140473505,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140473505,"alleles":["G","C"],"feature_type":"variation","strand":1},{"alleles":["T","C"],"end":140473508,"feature_type":"variation","strand":1,"source":"dbSNP","start":140473508,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs896250514"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1020829696","source":"dbSNP","start":140473514,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140473514,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1332225680","seq_region_name":"7","source":"dbSNP","start":140473518,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TT","T"],"end":140473519,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794996744","feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140473521,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473521},{"start":140473522,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140473522,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794996832","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794996881","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473524,"feature_type":"variation","strand":1,"end":140473524,"alleles":["A","G"]},{"start":140473524,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AATA","-"],"end":140473527,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1794996940","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140473525,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473525,"clinical_significance":[],"seq_region_name":"7","id":"rs1585494776"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473529,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140473529,"clinical_significance":[],"seq_region_name":"7","id":"rs966576067"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140473533,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473533,"clinical_significance":[],"id":"rs1325977911","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1013319407","clinical_significance":[],"end":140473534,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140473534,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140473543,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","T"],"end":140473543,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1391670462","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1324746507","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473550,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140473550},{"clinical_significance":[],"seq_region_name":"7","id":"rs1023370195","source":"dbSNP","start":140473551,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140473551,"alleles":["C","G","T"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473553,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GCAG","G"],"end":140473556,"seq_region_name":"7","id":"rs1322526860","clinical_significance":[]},{"seq_region_name":"7","id":"rs969238033","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473557,"source":"dbSNP","strand":1,"feature_type":"variation","end":140473557,"alleles":["T","C"]},{"end":140473560,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140473560,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1156648993","clinical_significance":[]},{"seq_region_name":"7","id":"rs977405113","clinical_significance":[],"start":140473565,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140473565,"alleles":["C","A","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1223185914","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473566,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140473566},{"clinical_significance":[],"seq_region_name":"7","id":"rs1395684928","feature_type":"variation","strand":1,"end":140473567,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473567},{"clinical_significance":[],"seq_region_name":"7","id":"rs73735279","source":"dbSNP","start":140473572,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C","G"],"end":140473572,"feature_type":"variation","strand":1},{"id":"rs1794998408","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473573,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140473573},{"id":"rs1794998500","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473577,"source":"dbSNP","strand":1,"feature_type":"variation","end":140473579,"alleles":["TTT","TT"]},{"source":"dbSNP","start":140473590,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140473590,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794998611"},{"seq_region_name":"7","id":"rs1252472238","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473593,"source":"dbSNP","strand":1,"feature_type":"variation","end":140473593,"alleles":["T","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794998787","alleles":["AC","-"],"end":140473601,"feature_type":"variation","strand":1,"source":"dbSNP","start":140473600,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473601,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140473601,"seq_region_name":"7","id":"rs1209551465","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140473602,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473602,"clinical_significance":[],"seq_region_name":"7","id":"rs1585494881"},{"alleles":["A","G"],"end":140473603,"strand":1,"feature_type":"variation","start":140473603,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1026941346","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473604,"source":"dbSNP","strand":1,"feature_type":"variation","end":140473604,"alleles":["T","C"],"id":"rs1282569032","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1204972937","feature_type":"variation","strand":1,"end":140473613,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473613},{"clinical_significance":[],"seq_region_name":"7","id":"rs1318884719","feature_type":"variation","strand":1,"alleles":["G","-"],"end":140473616,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473616},{"id":"rs1794999352","seq_region_name":"7","clinical_significance":[],"start":140473618,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140473618,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794999395","end":140473625,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140473625,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140473627,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473627,"source":"dbSNP","id":"rs1213648431","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs368801583","seq_region_name":"7","end":140473629,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140473629,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140473630,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473630,"clinical_significance":[],"seq_region_name":"7","id":"rs1232769267"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1794999561","source":"dbSNP","start":140473633,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140473633,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140473634,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473634,"clinical_significance":[],"seq_region_name":"7","id":"rs1242060386"},{"seq_region_name":"7","id":"rs1794999703","clinical_significance":[],"strand":1,"feature_type":"variation","end":140473637,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473637,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs982810505","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473640,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140473640},{"source":"dbSNP","start":140473641,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140473641,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1430988616"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1327894703","feature_type":"variation","strand":1,"end":140473646,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473646},{"seq_region_name":"7","id":"rs960047902","clinical_significance":[],"start":140473651,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140473651,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140473656,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140473660,"alleles":["TTTTT","TTTT","TTTTTT"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1794999939"},{"source":"dbSNP","start":140473661,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140473661,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795000007"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473662,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140473662,"clinical_significance":[],"seq_region_name":"7","id":"rs1490642754"},{"seq_region_name":"7","id":"rs992021271","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140473665,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473665,"source":"dbSNP"},{"source":"dbSNP","start":140473667,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140473667,"alleles":["A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1267270416"},{"id":"rs915988326","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473668,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140473668},{"seq_region_name":"7","id":"rs1795000366","clinical_significance":[],"strand":1,"feature_type":"variation","end":140473672,"alleles":["TAT","TATAT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473670,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs975497931","source":"dbSNP","start":140473672,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140473672,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140473676,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473676,"source":"dbSNP","seq_region_name":"7","id":"rs1795000420","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1409619327","alleles":["C","G","T"],"end":140473680,"feature_type":"variation","strand":1,"source":"dbSNP","start":140473680,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473681,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140473681,"seq_region_name":"7","id":"rs879257140","clinical_significance":[]},{"clinical_significance":[],"id":"rs1398461192","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473682,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140473682},{"seq_region_name":"7","id":"rs2130354434","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140473683,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473683,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130354450","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473684,"feature_type":"variation","strand":1,"alleles":["ATATATA","ATATA"],"end":140473690},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473685,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140473685,"clinical_significance":[],"id":"rs1795000704","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140473707,"alleles":["TATATACTTGTTAGAAAAAGGTA","TA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473685,"source":"dbSNP","id":"rs1240645498","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140473687,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140473687,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1192767064"},{"seq_region_name":"7","id":"rs1795000880","clinical_significance":[],"strand":1,"feature_type":"variation","end":140473689,"alleles":["T","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473689,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1585495031","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473692,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140473692},{"seq_region_name":"7","id":"rs1486176383","clinical_significance":[],"end":140473694,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140473694,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473695,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140473695,"seq_region_name":"7","id":"rs1282953409","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1209317169","feature_type":"variation","strand":1,"end":140473701,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473701},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473702,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AAGGTAGAA","AA"],"end":140473710,"seq_region_name":"7","id":"rs1347859525","clinical_significance":[]},{"alleles":["A","C"],"end":140473703,"feature_type":"variation","strand":1,"source":"dbSNP","start":140473703,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1278980568"},{"id":"rs1048556924","seq_region_name":"7","clinical_significance":[],"alleles":["G","A","C","T"],"end":140473704,"strand":1,"feature_type":"variation","start":140473704,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs947596950","clinical_significance":[],"start":140473706,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C","G"],"end":140473706,"strand":1,"feature_type":"variation"},{"start":140473708,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140473708,"alleles":["G","-"],"strand":1,"feature_type":"variation","id":"rs1795002022","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140473711,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140473711,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795002099"},{"seq_region_name":"7","id":"rs1795002202","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473712,"source":"dbSNP","strand":1,"feature_type":"variation","end":140473712,"alleles":["G","GGG"]},{"start":140473714,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140473714,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs908815218","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795002292","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140473715,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473715},{"end":140473716,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140473716,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs940228955"},{"source":"dbSNP","start":140473717,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140473717,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1429612772"},{"start":140473718,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140473718,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1041305862","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140473719,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473719,"clinical_significance":[],"seq_region_name":"7","id":"rs1157670791"},{"clinical_significance":[],"seq_region_name":"7","id":"rs377194381","feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140473721,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473721},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473722,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140473722,"clinical_significance":[],"id":"rs1795002854","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795002937","clinical_significance":[],"start":140473724,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140473724,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1795003016","clinical_significance":[],"alleles":["G","A"],"end":140473725,"strand":1,"feature_type":"variation","start":140473725,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795003111","clinical_significance":[],"alleles":["T","G"],"end":140473727,"strand":1,"feature_type":"variation","start":140473727,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140473729,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140473729,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795003175","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs10279172","source":"dbSNP","start":140473730,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140473730,"alleles":["T","C","G"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140473732,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473732,"source":"dbSNP","seq_region_name":"7","id":"rs1795003450","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1301195913","end":140473735,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140473735,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795003661","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473739,"feature_type":"variation","strand":1,"end":140473739,"alleles":["T","C"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473740,"source":"dbSNP","strand":1,"feature_type":"variation","end":140473742,"alleles":["CCC","CC"],"seq_region_name":"7","id":"rs1171217546","clinical_significance":[]},{"end":140473743,"alleles":["CCA","CCACCA"],"strand":1,"feature_type":"variation","start":140473741,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795003881","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140473744,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473744,"clinical_significance":[],"seq_region_name":"7","id":"rs1052128025"},{"strand":1,"feature_type":"variation","end":140473746,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473746,"source":"dbSNP","seq_region_name":"7","id":"rs1417489322","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473747,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140473747,"seq_region_name":"7","id":"rs2130354877","clinical_significance":[]},{"end":140473748,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140473748,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1049977903","clinical_significance":[]},{"end":140473749,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140473749,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1167516809","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795004289","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473751,"source":"dbSNP","strand":1,"feature_type":"variation","end":140473751,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1344707372","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473753,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140473753},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473754,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140473754,"seq_region_name":"7","id":"rs1260027720","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473756,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GC","GCGC"],"end":140473757,"seq_region_name":"7","id":"rs1186329147","clinical_significance":[]},{"seq_region_name":"7","id":"rs1410208956","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473758,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140473758},{"end":140473759,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140473759,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1280364475","clinical_significance":[]},{"start":140473761,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140473761,"alleles":["G","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795004734","clinical_significance":[]},{"clinical_significance":[],"id":"rs145430123","seq_region_name":"7","alleles":["C","T"],"end":140473763,"feature_type":"variation","strand":1,"source":"dbSNP","start":140473763,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1010711917","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A","C","T"],"end":140473764,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473764},{"clinical_significance":[],"seq_region_name":"7","id":"rs200166752","feature_type":"variation","strand":1,"end":140473766,"alleles":["GGG","GG"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473764},{"alleles":["G","A"],"end":140473765,"feature_type":"variation","strand":1,"source":"dbSNP","start":140473765,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs752595820"},{"source":"dbSNP","start":140473766,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140473766,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1270307567","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473767,"feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140473767,"clinical_significance":[],"seq_region_name":"7","id":"rs1585495239"},{"start":140473769,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140473769,"alleles":["G","C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795005363","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473770,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140473770,"clinical_significance":[],"id":"rs1020715135","seq_region_name":"7"},{"id":"rs1222163662","seq_region_name":"7","clinical_significance":[],"end":140473771,"alleles":["T","C","G"],"strand":1,"feature_type":"variation","start":140473771,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795005553","clinical_significance":[],"alleles":["T","C"],"end":140473772,"strand":1,"feature_type":"variation","start":140473772,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1283602938","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473775,"source":"dbSNP","strand":1,"feature_type":"variation","end":140473775,"alleles":["C","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473779,"feature_type":"variation","strand":1,"end":140473779,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs192113631"},{"id":"rs1795005773","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140473780,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473780,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1003436171","clinical_significance":[],"start":140473781,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A","C"],"end":140473781,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795005919","source":"dbSNP","start":140473787,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140473787,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140473788,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A","G"],"end":140473788,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585495276"},{"seq_region_name":"7","id":"rs1795006058","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473789,"source":"dbSNP","strand":1,"feature_type":"variation","end":140473789,"alleles":["T","C"]},{"end":140473791,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140473791,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795006135","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140473795,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473795,"source":"dbSNP","seq_region_name":"7","id":"rs1034939610","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795006260","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["CT","-"],"end":140473801,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473800,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795006331","end":140473801,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140473801,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140473804,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140473804,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795006398","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473808,"source":"dbSNP","strand":1,"feature_type":"variation","end":140473808,"alleles":["C","A","T"],"seq_region_name":"7","id":"rs1354585676","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1335411272","end":140473810,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140473810,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140473812,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140473812,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1225439756","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795006657","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473814,"source":"dbSNP","strand":1,"feature_type":"variation","end":140473814,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1298631401","clinical_significance":[],"alleles":["A","G"],"end":140473815,"strand":1,"feature_type":"variation","start":140473815,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs182254568","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473819,"source":"dbSNP","strand":1,"feature_type":"variation","end":140473819,"alleles":["C","A","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs995354541","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140473820,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473820},{"seq_region_name":"7","id":"rs1795006851","clinical_significance":[],"start":140473825,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140473825,"alleles":["C","G","T"],"strand":1,"feature_type":"variation"},{"id":"rs1027198701","seq_region_name":"7","clinical_significance":[],"start":140473828,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140473828,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs991470057","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140473829,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473829,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473830,"feature_type":"variation","strand":1,"alleles":["AAAAA","AAA"],"end":140473834,"clinical_significance":[],"seq_region_name":"7","id":"rs1490289820"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473831,"source":"dbSNP","strand":1,"feature_type":"variation","end":140473831,"alleles":["A","G"],"seq_region_name":"7","id":"rs1163060901","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795007179","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140473832,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473832,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140473838,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473838,"source":"dbSNP","seq_region_name":"7","id":"rs1795007237","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795007308","feature_type":"variation","strand":1,"end":140473839,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473839},{"clinical_significance":[],"id":"rs1475053625","seq_region_name":"7","source":"dbSNP","start":140473845,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140473845,"alleles":["A","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1409197681","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140473846,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473846},{"clinical_significance":[],"id":"rs1795007614","seq_region_name":"7","source":"dbSNP","start":140473847,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140473847,"alleles":["C","G"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473848,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","G","T"],"end":140473848,"seq_region_name":"7","id":"rs1182905075","clinical_significance":[]},{"seq_region_name":"7","id":"rs1234274240","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473849,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140473849},{"source":"dbSNP","start":140473852,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140473852,"alleles":["T","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1468245708"},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140473855,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473855,"source":"dbSNP","id":"rs1795007950","seq_region_name":"7","clinical_significance":[]},{"id":"rs1795008009","seq_region_name":"7","clinical_significance":[],"end":140473856,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140473856,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1176235120","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140473860,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473860,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473861,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140473861,"seq_region_name":"7","id":"rs951343723","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140473862,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473862,"clinical_significance":[],"seq_region_name":"7","id":"rs1320851707"},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140473863,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473863,"clinical_significance":[],"seq_region_name":"7","id":"rs1385373414"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473865,"source":"dbSNP","strand":1,"feature_type":"variation","end":140473865,"alleles":["G","A"],"seq_region_name":"7","id":"rs566652980","clinical_significance":[]},{"alleles":["C","T"],"end":140473866,"feature_type":"variation","strand":1,"source":"dbSNP","start":140473866,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795008705"},{"source":"dbSNP","start":140473868,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140473868,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs952751538"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795008822","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473869,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140473869},{"clinical_significance":[],"id":"rs984304256","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473878,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140473878},{"clinical_significance":[],"id":"rs1441645366","seq_region_name":"7","end":140473880,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140473880,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs908741616","source":"dbSNP","start":140473883,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140473883,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs940153467","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140473884,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473884,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473887,"feature_type":"variation","strand":1,"end":140473887,"alleles":["G","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795009134"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473890,"feature_type":"variation","strand":1,"end":140473890,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795009190"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140473892,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473892,"source":"dbSNP","seq_region_name":"7","id":"rs1324075526","clinical_significance":[]},{"source":"dbSNP","start":140473893,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140473893,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs977041404"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473893,"feature_type":"variation","strand":1,"end":140473899,"alleles":["GAGAGAG","GAGAG"],"clinical_significance":[],"seq_region_name":"7","id":"rs1461148190"},{"clinical_significance":[],"seq_region_name":"7","id":"rs374008701","feature_type":"variation","strand":1,"end":140473895,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473895},{"alleles":["GAGAGGAAAATCGCTGGAACCCAGGAGATGGCGATTGCACCGAG","GAGAGGAAAATCGCTGGAACCCAGGAGATGGCGATTGCACCGAGAGGAAAATCGCTGGAACCCAGGAGATGGCGATTGCACCGAG"],"end":140473938,"feature_type":"variation","strand":1,"source":"dbSNP","start":140473895,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795009532"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795009595","end":140473900,"alleles":["GG","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140473899,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1161790258","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140473900,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473900},{"source":"dbSNP","start":140473901,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140473901,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs922872272","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795009753","feature_type":"variation","strand":1,"alleles":["AAATCGCTG","-"],"end":140473910,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473902},{"clinical_significance":[],"seq_region_name":"7","id":"rs1417839547","end":140473906,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140473906,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473907,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C","T"],"end":140473907,"seq_region_name":"7","id":"rs932310289","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795009981","clinical_significance":[],"start":140473909,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140473909,"alleles":["T","-"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140473911,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140473911,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1049380363"},{"end":140473922,"alleles":["GAACCCAGGAGA","GA"],"strand":1,"feature_type":"variation","start":140473911,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795010130","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795010217","clinical_significance":[],"start":140473912,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140473912,"strand":1,"feature_type":"variation"},{"start":140473913,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140473913,"strand":1,"feature_type":"variation","id":"rs1585495469","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585495477","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473914,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140473914},{"clinical_significance":[],"seq_region_name":"7","id":"rs965384350","feature_type":"variation","strand":1,"end":140473915,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473915},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473923,"feature_type":"variation","strand":1,"end":140473923,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585495487"},{"clinical_significance":[],"seq_region_name":"7","id":"rs893559219","source":"dbSNP","start":140473925,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140473925,"alleles":["G","A"],"feature_type":"variation","strand":1},{"end":140473926,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140473926,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs145279462"},{"alleles":["G","A","T"],"end":140473927,"strand":1,"feature_type":"variation","start":140473927,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs751979672","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1308783836","source":"dbSNP","start":140473929,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A","C"],"end":140473929,"feature_type":"variation","strand":1},{"end":140473930,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","start":140473930,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1314917904","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585495521","clinical_significance":[],"strand":1,"feature_type":"variation","end":140473931,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473931,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1383704133","seq_region_name":"7","source":"dbSNP","start":140473933,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C","G"],"end":140473933,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795011292","feature_type":"variation","strand":1,"end":140473934,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473934},{"seq_region_name":"7","id":"rs1795011366","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473935,"source":"dbSNP","strand":1,"feature_type":"variation","end":140473935,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs149169645","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473936,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140473936},{"seq_region_name":"7","id":"rs1795011563","clinical_significance":[],"start":140473937,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AGCCAAG","AG"],"end":140473943,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs571207928","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140473938,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473938,"source":"dbSNP"},{"end":140473939,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140473939,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795011809"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473940,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140473940,"seq_region_name":"7","id":"rs978967439","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795011972","seq_region_name":"7","source":"dbSNP","start":140473943,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140473943,"feature_type":"variation","strand":1},{"end":140473945,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140473945,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795012080","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs924752762","feature_type":"variation","strand":1,"end":140473947,"alleles":["G","A","C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473947},{"start":140473947,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","-"],"end":140473947,"strand":1,"feature_type":"variation","id":"rs1301386952","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140473948,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473948,"clinical_significance":[],"seq_region_name":"7","id":"rs1795012455"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1362988685","feature_type":"variation","strand":1,"alleles":["T","A","G"],"end":140473950,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473950},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473951,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140473951,"seq_region_name":"7","id":"rs1795012618","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["CACTGCAC","C"],"end":140473958,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473951,"source":"dbSNP","id":"rs1290994927","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795012807","clinical_significance":[],"strand":1,"feature_type":"variation","end":140473952,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473952,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473955,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140473955,"id":"rs934829325","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140473956,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473956,"clinical_significance":[],"seq_region_name":"7","id":"rs1196773406"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795013099","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140473958,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473958},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473960,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140473960,"clinical_significance":[],"seq_region_name":"7","id":"rs1585495592"},{"seq_region_name":"7","id":"rs1795013293","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473962,"source":"dbSNP","strand":1,"feature_type":"variation","end":140473962,"alleles":["A","AA"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473964,"source":"dbSNP","strand":1,"feature_type":"variation","end":140473964,"alleles":["C","T"],"id":"rs1795013359","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1344987090","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473967,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GGGCAACAACAG","G"],"end":140473978},{"seq_region_name":"7","id":"rs1275595722","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140473968,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473968,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473968,"source":"dbSNP","strand":1,"feature_type":"variation","end":140473970,"alleles":["GGC","-"],"seq_region_name":"7","id":"rs1174773297","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1437169051","feature_type":"variation","strand":1,"end":140473971,"alleles":["A","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473971},{"strand":1,"feature_type":"variation","end":140473973,"alleles":["C","A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473973,"source":"dbSNP","id":"rs1795013712","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473974,"feature_type":"variation","strand":1,"alleles":["AA","A"],"end":140473975,"clinical_significance":[],"id":"rs1396341239","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1795013849","seq_region_name":"7","alleles":["AGCGAAACTCCGTCTCAAAAAAAAAAAAAAAAGAAAGAAAG","AG"],"end":140474017,"feature_type":"variation","strand":1,"source":"dbSNP","start":140473977,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473977,"feature_type":"variation","strand":1,"end":140474021,"alleles":["AGCGAAACTCCGTCTCAAAAAAAAAAAAAAAAGAAAGAAAGAAAG","AG"],"clinical_significance":[],"seq_region_name":"7","id":"rs1191271201"},{"end":140473979,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140473979,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1436408636"},{"seq_region_name":"7","id":"rs1795014065","clinical_significance":[],"end":140474005,"alleles":["CGAAACTCCGTCTCAAAAAAAAAAAAA","-"],"strand":1,"feature_type":"variation","start":140473979,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs2130356351","seq_region_name":"7","alleles":["AAA","AAAA"],"end":140473983,"feature_type":"variation","strand":1,"source":"dbSNP","start":140473981,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140473982,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473982,"source":"dbSNP","seq_region_name":"7","id":"rs1795014146","clinical_significance":[]},{"start":140473983,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140473983,"alleles":["A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795014224","clinical_significance":[]},{"end":140473984,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140473984,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1261919429"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1032199539","feature_type":"variation","strand":1,"end":140473987,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473987},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473988,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140473988,"seq_region_name":"7","id":"rs1484744793","clinical_significance":[]},{"clinical_significance":[],"id":"rs1285077557","seq_region_name":"7","source":"dbSNP","start":140473989,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TCTC","TC"],"end":140473992,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1211464194","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473989,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TCTCAAAAA","-"],"end":140473997},{"clinical_significance":[],"id":"rs1350020352","seq_region_name":"7","source":"dbSNP","start":140473989,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140474005,"alleles":["TCTCAAAAAAAAAAAAA","-"],"feature_type":"variation","strand":1},{"end":140473992,"alleles":["CTC","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140473990,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1278262503","seq_region_name":"7"},{"id":"rs1232711984","seq_region_name":"7","clinical_significance":[],"start":140473991,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140473991,"alleles":["T","-"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1374246126","end":140473991,"alleles":["T","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140473991,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1308156785","feature_type":"variation","strand":1,"end":140473993,"alleles":["TCA","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473991},{"alleles":["TCAA","-"],"end":140473994,"feature_type":"variation","strand":1,"source":"dbSNP","start":140473991,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1297920263"},{"strand":1,"feature_type":"variation","end":140473995,"alleles":["TCAAA","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473991,"source":"dbSNP","seq_region_name":"7","id":"rs1380766259","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140473996,"alleles":["TCAAAA","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473991,"source":"dbSNP","seq_region_name":"7","id":"rs1340262726","clinical_significance":[]},{"end":140473998,"alleles":["TCAAAAAA","-"],"strand":1,"feature_type":"variation","start":140473991,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1313925252","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140474000,"alleles":["TCAAAAAAAA","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473991,"source":"dbSNP","seq_region_name":"7","id":"rs1795015716","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795015791","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["TCAAAAAAAAA","-"],"end":140474001,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473991,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473991,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TCAAAAAAAAAAA","-"],"end":140474003,"seq_region_name":"7","id":"rs1795015890","clinical_significance":[]},{"start":140473991,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TCAAAAAAAAAAAAAAA","-"],"end":140474007,"strand":1,"feature_type":"variation","id":"rs1417147577","seq_region_name":"7","clinical_significance":[]},{"id":"rs1795016060","seq_region_name":"7","clinical_significance":[],"start":140473992,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140473991,"alleles":["-","A"],"strand":1,"feature_type":"variation"},{"id":"rs1173572082","seq_region_name":"7","clinical_significance":[],"start":140473992,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140473992,"alleles":["C","-"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473992,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","G"],"end":140473992,"id":"rs1373174971","seq_region_name":"7","clinical_significance":[]},{"id":"rs1795016339","seq_region_name":"7","clinical_significance":[],"end":140473993,"alleles":["CA","-"],"strand":1,"feature_type":"variation","start":140473992,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1465061510","feature_type":"variation","strand":1,"end":140473994,"alleles":["CAA","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473992},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795016489","feature_type":"variation","strand":1,"end":140473995,"alleles":["CAAA","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473992},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473992,"feature_type":"variation","strand":1,"alleles":["CAAAA","-"],"end":140473996,"clinical_significance":[],"seq_region_name":"7","id":"rs1795016565"},{"feature_type":"variation","strand":1,"end":140474000,"alleles":["CAAAAAAAA","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473992,"clinical_significance":[],"id":"rs1795016669","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["CAAAAAAAAAAA","-"],"end":140474003,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473992,"clinical_significance":[],"seq_region_name":"7","id":"rs1795016759"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1243376960","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473992,"feature_type":"variation","strand":1,"alleles":["CAAAAAAAAAAAA","-"],"end":140474004},{"source":"dbSNP","start":140473993,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140473993,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1294288318"},{"clinical_significance":[],"seq_region_name":"7","id":"rs750043239","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473993,"feature_type":"variation","strand":1,"end":140474008,"alleles":["AAAAAAAAAAAAAAAA","AA","AAA","AAAAA","AAAAAA","AAAAAAA","AAAAAAAA","AAAAAAAAA","AAAAAAAAAA","AAAAAAAAAAA","AAAAAAAAAAAA","AAAAAAAAAAAAA","AAAAAAAAAAAAAA","AAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAA"]},{"seq_region_name":"7","id":"rs1795017635","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["AAAAAAAAAAAAAAAA","-"],"end":140474008,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473993,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1727982783","seq_region_name":"7","feature_type":"variation","strand":1,"end":140474024,"alleles":["AAAAAAAAAAAAAAAAGAAAGAAAGAAAGAAA","AAA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473993},{"seq_region_name":"7","id":"rs113594767","clinical_significance":[],"end":140473994,"alleles":["A","G","T"],"strand":1,"feature_type":"variation","start":140473994,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140473995,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473995,"source":"dbSNP","seq_region_name":"7","id":"rs1795017915","clinical_significance":[]},{"id":"rs1334033634","seq_region_name":"7","clinical_significance":[],"alleles":["A","G"],"end":140473996,"strand":1,"feature_type":"variation","start":140473996,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140473996,"alleles":["-","G"],"strand":1,"feature_type":"variation","start":140473997,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1491051646","seq_region_name":"7","clinical_significance":[]},{"end":140473997,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140473997,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1396548400"},{"id":"rs1795018215","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473997,"source":"dbSNP","strand":1,"feature_type":"variation","end":140473997,"alleles":["A","AGA"]},{"seq_region_name":"7","id":"rs1795018281","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["AAAAAAAAAAAAGAAAGAAA","AAA"],"end":140474016,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473997,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473998,"feature_type":"variation","strand":1,"end":140473997,"alleles":["-","GG"],"clinical_significance":[],"seq_region_name":"7","id":"rs1392515909"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1463719223","feature_type":"variation","strand":1,"end":140473998,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473998},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795018389","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473998,"feature_type":"variation","strand":1,"end":140474000,"alleles":["AAA","AAAGAAAGAAA"]},{"clinical_significance":[],"id":"rs1795018457","seq_region_name":"7","alleles":["AAAAAAAAAAAGAAA","AAA"],"end":140474012,"feature_type":"variation","strand":1,"source":"dbSNP","start":140473998,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1299428999","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["AAAAAAAAAAAGAAAGAAA","AAA"],"end":140474016,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140473998,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1795018604","seq_region_name":"7","end":140474032,"alleles":["AAAAAAAAAAAGAAAGAAAGAAAGAAAGAAAGAAA","AAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140473998,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140473999,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["-","G"],"end":140473998,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795018702","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140473999,"alleles":["A","C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140473999,"clinical_significance":[],"seq_region_name":"7","id":"rs1181156204"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795018944","end":140473999,"alleles":["-","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140474000,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140474000,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474000,"source":"dbSNP","seq_region_name":"7","id":"rs1415423669","clinical_significance":[]},{"start":140474000,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","AGA"],"end":140474000,"strand":1,"feature_type":"variation","id":"rs1795019164","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474001,"feature_type":"variation","strand":1,"alleles":["-","G"],"end":140474000,"clinical_significance":[],"seq_region_name":"7","id":"rs1165199260"},{"clinical_significance":[],"seq_region_name":"7","id":"rs868439209","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474001,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140474001},{"end":140474002,"alleles":["AA","AAGGAA"],"strand":1,"feature_type":"variation","start":140474001,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1554450271","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474001,"feature_type":"variation","strand":1,"alleles":["AAAAAAAAGAAAGAAAGAAAGAAAGAAAGAAA","AAA"],"end":140474032,"clinical_significance":[],"id":"rs1186701160","seq_region_name":"7"},{"alleles":["AAAAAAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAA","AAA"],"end":140474036,"feature_type":"variation","strand":1,"source":"dbSNP","start":140474001,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1438374961"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795019770","source":"dbSNP","start":140474001,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140474044,"alleles":["AAAAAAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAA","AAA"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1554450277","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474002,"feature_type":"variation","strand":1,"end":140474001,"alleles":["-","G","GAAAGAAAGAAAGAAAG","GAAAGGAAGAAAGAAAGGAAGAAAGAAAGGAAGAAAGAAAGGAAGAAAGAAAGGAAG","GAAAGGAAGAAAGAAAGGAAGAAAGAAAGGAAGAAAGAAAGGAAGAAAGAAAGGAAGAAAG","GAAG"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474002,"feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140474002,"clinical_significance":[],"seq_region_name":"7","id":"rs1338102359"},{"strand":1,"feature_type":"variation","alleles":["AA","AAGAA","AAGAAAGAA"],"end":140474003,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474002,"source":"dbSNP","seq_region_name":"7","id":"rs1563096704","clinical_significance":[]},{"clinical_significance":[],"id":"rs1252740224","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474002,"feature_type":"variation","strand":1,"end":140474004,"alleles":["AAA","AAAGAAA","AAAGAAAGAAA","AAAGAAAGAAAGAAA","AAAGAAAGAAAGAAAGAAAGAAA","AAAGAAAGAAAGAAAGAAAGAAAGAAA"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474002,"source":"dbSNP","strand":1,"feature_type":"variation","end":140474012,"alleles":["AAAAAAAGAAA","AAA"],"seq_region_name":"7","id":"rs1215815161","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1333101137","end":140474016,"alleles":["AAAAAAAGAAAGAAA","AAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140474002,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["AAAAAAAGAAAGAAAGAAA","AAA"],"end":140474020,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474002,"source":"dbSNP","id":"rs1292202428","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["AAAAAAAGAAAGAAAGAAAGAAA","AAA"],"end":140474024,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474002,"clinical_significance":[],"seq_region_name":"7","id":"rs1240357211"},{"feature_type":"variation","strand":1,"alleles":["AAAAAAAGAAAGAAAGAAAGAAAGAAA","AAA"],"end":140474028,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474002,"clinical_significance":[],"seq_region_name":"7","id":"rs1563096719"},{"source":"dbSNP","start":140474002,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140474032,"alleles":["AAAAAAAGAAAGAAAGAAAGAAAGAAAGAAA","AAA"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1563096725"},{"clinical_significance":[],"id":"rs1563096731","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474002,"feature_type":"variation","strand":1,"alleles":["AAAAAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAA","AAA"],"end":140474036},{"seq_region_name":"7","id":"rs1563096735","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474002,"source":"dbSNP","strand":1,"feature_type":"variation","end":140474044,"alleles":["AAAAAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAA","AAA"]},{"seq_region_name":"7","id":"rs1795021343","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["-","GG"],"end":140474002,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474003,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1398934969","source":"dbSNP","start":140474003,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C","G"],"end":140474003,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["A","AGAAAGA"],"end":140474003,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474003,"clinical_significance":[],"id":"rs1795021558","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1308510437","clinical_significance":[],"alleles":["AAAAAAGAAA","AAA"],"end":140474012,"strand":1,"feature_type":"variation","start":140474003,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["AAAAAAGAAAGAAA","AAA"],"end":140474016,"feature_type":"variation","strand":1,"source":"dbSNP","start":140474003,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795021703"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563096740","source":"dbSNP","start":140474003,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140474032,"alleles":["AAAAAAGAAAGAAAGAAAGAAAGAAAGAAA","AAA"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563096745","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474003,"feature_type":"variation","strand":1,"alleles":["AAAAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAA","AAA"],"end":140474036},{"seq_region_name":"7","id":"rs1443848995","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474003,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AAAAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAA","AAA"],"end":140474044},{"end":140474003,"alleles":["-","G"],"strand":1,"feature_type":"variation","start":140474004,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795021967","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140474004,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474004,"clinical_significance":[],"seq_region_name":"7","id":"rs1253744124"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563096758","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474004,"feature_type":"variation","strand":1,"alleles":["AAAAAGAAA","AAA"],"end":140474012},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474004,"feature_type":"variation","strand":1,"alleles":["AAAAAGAAAGAAA","AAA"],"end":140474016,"clinical_significance":[],"seq_region_name":"7","id":"rs1326107788"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1462719014","source":"dbSNP","start":140474004,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AAAAAGAAAGAAAGAAA","AAA"],"end":140474020,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795022470","alleles":["AAAAAGAAAGAAAGAAAGAAAGAAA","AAA"],"end":140474028,"feature_type":"variation","strand":1,"source":"dbSNP","start":140474004,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474004,"feature_type":"variation","strand":1,"end":140474032,"alleles":["AAAAAGAAAGAAAGAAAGAAAGAAAGAAA","AAA"],"clinical_significance":[],"seq_region_name":"7","id":"rs1563096766"},{"strand":1,"feature_type":"variation","alleles":["AAAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAA","AAA"],"end":140474036,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474004,"source":"dbSNP","seq_region_name":"7","id":"rs1388283535","clinical_significance":[]},{"start":140474004,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140474040,"alleles":["AAAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAA","AAA"],"strand":1,"feature_type":"variation","id":"rs1162494175","seq_region_name":"7","clinical_significance":[]},{"end":140474044,"alleles":["AAAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAA","AAA"],"strand":1,"feature_type":"variation","start":140474004,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1470470209","clinical_significance":[]},{"end":140474048,"alleles":["AAAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAA","AAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140474004,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1365402017"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1176719470","alleles":["AAAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAA","AAA"],"end":140474052,"feature_type":"variation","strand":1,"source":"dbSNP","start":140474004,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1439113885","feature_type":"variation","strand":1,"alleles":["-","G"],"end":140474004,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474005},{"id":"rs865882330","seq_region_name":"7","clinical_significance":[],"end":140474005,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140474005,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140474005,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140474005,"alleles":["A","AGA"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795023425"},{"feature_type":"variation","strand":1,"alleles":["AAA","AAAGAAAGAAA"],"end":140474007,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474005,"clinical_significance":[],"seq_region_name":"7","id":"rs1554450298"},{"id":"rs1195704000","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140474012,"alleles":["AAAAGAAA","AAA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474005,"source":"dbSNP"},{"source":"dbSNP","start":140474005,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140474016,"alleles":["AAAAGAAAGAAA","AAA"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1467345900"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474005,"source":"dbSNP","strand":1,"feature_type":"variation","end":140474020,"alleles":["AAAAGAAAGAAAGAAA","AAA"],"seq_region_name":"7","id":"rs1289594231","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1206158270","end":140474024,"alleles":["AAAAGAAAGAAAGAAAGAAA","AAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140474005,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["AAAAGAAAGAAAGAAAGAAAGAAA","AAA"],"end":140474028,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474005,"source":"dbSNP","seq_region_name":"7","id":"rs1353290809","clinical_significance":[]},{"alleles":["AAAAGAAAGAAAGAAAGAAAGAAAGAAA","AAA"],"end":140474032,"strand":1,"feature_type":"variation","start":140474005,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1259426769","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs761718411","clinical_significance":[],"start":140474005,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140474036,"alleles":["AAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAA","AAA"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474005,"source":"dbSNP","strand":1,"feature_type":"variation","end":140474040,"alleles":["AAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAA","AAA"],"id":"rs1375469134","seq_region_name":"7","clinical_significance":[]},{"alleles":["AAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAA","AAA"],"end":140474044,"strand":1,"feature_type":"variation","start":140474005,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1303557117","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1442632434","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474005,"feature_type":"variation","strand":1,"alleles":["AAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAA","AAA"],"end":140474048},{"seq_region_name":"7","id":"rs1329062553","clinical_significance":[],"start":140474005,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140474052,"alleles":["AAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAA","AAA"],"strand":1,"feature_type":"variation"},{"start":140474006,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140474005,"alleles":["-","CG","G","GAAAG","GAAAGAAAG","GAAAGAAAGAAAGAAAGGAAAGAAAGG","GG","GGAAGAAAGAAAGGAAGAAAGAAAGGAAGAAAGAAAGGAAGAAAGAAAGGAAG"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1554450296","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140474006,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474006,"source":"dbSNP","id":"rs1476535986","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1554450299","clinical_significance":[],"alleles":["A","ACA","AGA","AGAAAGAAAGAAAGAAAGAAAAAGAAAGA","AGAAAGAAAGAAAGAAAGAAAAAGAAAGAAAGA","AGAAGA","AGAAGAAAGA","AGGA"],"end":140474006,"strand":1,"feature_type":"variation","start":140474006,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474006,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AA","AAGAA","AAGAAAAAAAAGAAAGAAAGAAAGAAAGAAAAGAA","AAGAAAGAA","AAGAAAGAAAGAA","AAGAAAGAAAGAAAGAA","AAGAAAGAAAGAAAGAAAGAA","AAGAAAGAAAGAAAGAAAGAAAGAA","AAGAAAGAAAGAAAGAAAGAAAGAAAGAA"],"end":140474007,"seq_region_name":"7","id":"rs1554450297","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1336764327","source":"dbSNP","start":140474006,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140474008,"alleles":["AAA","AAAAAAAAGAAA","AAAAAAAGAAAGAAA","AAAAAAAGAAAGAAAGAAA","AAAAAAAGAAAGAAAGAAAGAAA","AAAAAAGAAA","AAAAAAGAAAGAAAGAAA","AAAAAAGAAAGAAAGAAAGAAAGAAAGAAA","AAAAAGAAA","AAAAGAAA","AAAAGAAAGAAA","AAAAGAAAGAAAGAAA","AAAAGAAAGAAAGAAAGAAAGAAAGAAA","AAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAATGAAAGAAAGAAA","AAATAAAGAAA"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140474006,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140474010,"alleles":["AAAGA","AAAGACAGAAAGA"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795025676"},{"start":140474006,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140474011,"alleles":["AAAGAA","AAAGAAGAAAGAAAGAA"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795025763","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474006,"feature_type":"variation","strand":1,"alleles":["AAAGAAA","AAAGAAATAAAGAAAGAAAGAAA"],"end":140474012,"clinical_significance":[],"seq_region_name":"7","id":"rs1795025832"},{"strand":1,"feature_type":"variation","end":140474034,"alleles":["AAAGAAAGAAAGAAAGAAAGAAAGAAAGA","AAAGAAAGAAAGAAAGAAAGAAAGAAAGACAGAAAGAAAGAAAGACAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474006,"source":"dbSNP","seq_region_name":"7","id":"rs1795025916","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs71272543","end":140474067,"alleles":["AAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA","AAAGAAAGAAAGAAAGAAAGAA","AAAGAAAGAAAGAAAGAAAGAAAGAA","AAAGAAAGAAAGAAAGAAAGAAAGAAAGAA","AAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA","AAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA","AAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA","AAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA","AAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA","AAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA","AAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA","AAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA","AAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA","AAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA","AAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA","AAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA","AAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA","AAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA","AAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA","AAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA","AAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA","AAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140474006,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1424576257","clinical_significance":[],"start":140474007,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["-","G","GG","GGAAGAAAGAAAGG"],"end":140474006,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1563096848","clinical_significance":[],"alleles":["A","AGGA"],"end":140474007,"strand":1,"feature_type":"variation","start":140474007,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585496107","end":140474007,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140474007,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["AAGAA","AA"],"end":140474011,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474007,"clinical_significance":[],"seq_region_name":"7","id":"rs1193482161"},{"seq_region_name":"7","id":"rs1486206042","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474007,"source":"dbSNP","strand":1,"feature_type":"variation","end":140474015,"alleles":["AAGAAAGAA","AA"]},{"seq_region_name":"7","id":"rs1260160598","clinical_significance":[],"start":140474007,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140474019,"alleles":["AAGAAAGAAAGAA","AA"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474007,"feature_type":"variation","strand":1,"alleles":["AAGAAAGAAAGAAAGAA","AA"],"end":140474023,"clinical_significance":[],"id":"rs1795027103","seq_region_name":"7"},{"end":140474027,"alleles":["AAGAAAGAAAGAAAGAAAGAA","AA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140474007,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1208672511"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795027225","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474007,"feature_type":"variation","strand":1,"alleles":["AAGAAAGAAAGAAAGAAAGAAAGAA","AA"],"end":140474031},{"end":140474035,"alleles":["AAGAAAGAAAGAAAGAAAGAAAGAAAGAA","AA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140474007,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795027282"},{"seq_region_name":"7","id":"rs1475679734","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474008,"source":"dbSNP","strand":1,"feature_type":"variation","end":140474008,"alleles":["A","C","G"]},{"seq_region_name":"7","id":"rs1440160212","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474008,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AGA","A"],"end":140474010},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474008,"source":"dbSNP","strand":1,"feature_type":"variation","end":140474026,"alleles":["AGAAAGAAAGAAAGAAAGA","AGAAAGAAAGAAAGAAAGAGAGAAAGAAAGAAAGAAAGA"],"seq_region_name":"7","id":"rs1795027510","clinical_significance":[]},{"seq_region_name":"7","id":"rs1384561839","clinical_significance":[],"start":140474008,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AGAAAGAAAGAAAGAAAGAAAGAAAGA","A"],"end":140474034,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140474008,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AGAAAGAAAGAAAGAAAGAAAGAAAGAAAGA","A"],"end":140474038,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795027624"},{"alleles":["AGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGA","A"],"end":140474042,"feature_type":"variation","strand":1,"source":"dbSNP","start":140474008,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795027709"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795027796","feature_type":"variation","strand":1,"alleles":["AGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGA","A"],"end":140474046,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474008},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474009,"source":"dbSNP","strand":1,"feature_type":"variation","end":140474009,"alleles":["G","A","C","T"],"id":"rs4725702","seq_region_name":"7","clinical_significance":[]},{"end":140474009,"alleles":["G","-"],"strand":1,"feature_type":"variation","start":140474009,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1341112545","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795028046","clinical_significance":[],"strand":1,"feature_type":"variation","end":140474009,"alleles":["G","GG"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474009,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1563096875","clinical_significance":[],"alleles":["GAAAG","-"],"end":140474013,"strand":1,"feature_type":"variation","start":140474009,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563096886","end":140474017,"alleles":["GAAAGAAAG","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140474009,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1795028499","seq_region_name":"7","clinical_significance":[],"start":140474009,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140474023,"alleles":["GAAAGAAAGAAAGAA","GAAAGAAAGAAAGAAGGAAAGAAAGAAAGAA"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474009,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GAAAGAAAGAAAGAAAG","-"],"end":140474025,"id":"rs1563096895","seq_region_name":"7","clinical_significance":[]},{"start":140474009,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140474029,"alleles":["GAAAGAAAGAAAGAAAGAAAG","-"],"strand":1,"feature_type":"variation","id":"rs1563096899","seq_region_name":"7","clinical_significance":[]},{"start":140474009,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["GAAAGAAAGAAAGAAAGAAAGAAAG","-"],"end":140474033,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1563096903","clinical_significance":[]},{"seq_region_name":"7","id":"rs1314591767","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140474010,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474010,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1217715094","source":"dbSNP","start":140474010,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140474012,"alleles":["AAA","AA","AAAA"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1563096913","clinical_significance":[],"end":140474016,"alleles":["AAAGAAA","AA"],"strand":1,"feature_type":"variation","start":140474010,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1394137323","source":"dbSNP","start":140474011,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140474011,"alleles":["A","C","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795029265","clinical_significance":[],"start":140474012,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140474012,"alleles":["A","C","G"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140474014,"alleles":["AGA","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474012,"source":"dbSNP","id":"rs1563096923","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795029463","clinical_significance":[],"alleles":["AGAAAGAAAGA","A"],"end":140474022,"strand":1,"feature_type":"variation","start":140474012,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1409148429","clinical_significance":[],"start":140474013,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140474012,"alleles":["-","AG"],"strand":1,"feature_type":"variation"},{"id":"rs4725703","seq_region_name":"7","clinical_significance":[],"alleles":["G","A","C"],"end":140474013,"strand":1,"feature_type":"variation","start":140474013,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140474013,"alleles":["G","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140474013,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1563096932"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795029774","feature_type":"variation","strand":1,"end":140474013,"alleles":["G","GG"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474013},{"end":140474014,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140474014,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795029931","clinical_significance":[]},{"clinical_significance":[],"id":"rs1330935175","seq_region_name":"7","source":"dbSNP","start":140474014,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140474016,"alleles":["AAA","AAAA"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["AAAGAAA","AAAGAAAAAGAAA"],"end":140474020,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474014,"clinical_significance":[],"seq_region_name":"7","id":"rs1554450313"},{"id":"rs1475713107","seq_region_name":"7","clinical_significance":[],"start":140474015,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C","G"],"end":140474015,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["AAGAAAG","AAGAAAGGAAGAAAG"],"end":140474021,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474015,"clinical_significance":[],"seq_region_name":"7","id":"rs1795030325"},{"id":"rs1407029425","seq_region_name":"7","clinical_significance":[],"start":140474015,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AAGAAAGAAAGAAAGAAAGAAAGAAAGAA","AA"],"end":140474043,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1454669438","clinical_significance":[],"alleles":["A","C","G"],"end":140474016,"strand":1,"feature_type":"variation","start":140474016,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["AGA","A"],"end":140474018,"feature_type":"variation","strand":1,"source":"dbSNP","start":140474016,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1420519053"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795030724","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474017,"feature_type":"variation","strand":1,"alleles":["-","AG"],"end":140474016},{"seq_region_name":"7","id":"rs970437926","clinical_significance":[],"start":140474017,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140474017,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1255696391","feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140474018,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474018},{"clinical_significance":[],"seq_region_name":"7","id":"rs1312962229","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474018,"feature_type":"variation","strand":1,"end":140474020,"alleles":["AAA","AAAA","AAAAGAAAA"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474018,"feature_type":"variation","strand":1,"alleles":["AAAGAAA","AAAGAAAAAGAAA"],"end":140474024,"clinical_significance":[],"seq_region_name":"7","id":"rs1554450318"},{"seq_region_name":"7","id":"rs1228852803","clinical_significance":[],"strand":1,"feature_type":"variation","end":140474019,"alleles":["A","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474019,"source":"dbSNP"},{"alleles":["AAGAA","AA"],"end":140474023,"feature_type":"variation","strand":1,"source":"dbSNP","start":140474019,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1339913561"},{"alleles":["AAGAAAGAA","AA"],"end":140474027,"feature_type":"variation","strand":1,"source":"dbSNP","start":140474019,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795031501"},{"alleles":["A","C","G"],"end":140474020,"feature_type":"variation","strand":1,"source":"dbSNP","start":140474020,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795031596"},{"seq_region_name":"7","id":"rs1795031703","clinical_significance":[],"strand":1,"feature_type":"variation","end":140474020,"alleles":["-","AG"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474021,"source":"dbSNP"},{"clinical_significance":[],"id":"rs980816964","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474021,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140474021},{"feature_type":"variation","strand":1,"end":140474021,"alleles":["G","GG"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474021,"clinical_significance":[],"seq_region_name":"7","id":"rs1226512524"},{"seq_region_name":"7","id":"rs1280070175","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474022,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AAA","A","AAAA","AAAAA"],"end":140474024},{"end":140474040,"alleles":["AAAGAAAGAAAGAAAGAAA","AAAGAAAGAAAGAAAGAAAAAGAAAGAAAGAAAGAAA"],"strand":1,"feature_type":"variation","start":140474022,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs2130358637","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140474023,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["-","T"],"end":140474022,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1398232085"},{"alleles":["A","C","G"],"end":140474023,"feature_type":"variation","strand":1,"source":"dbSNP","start":140474023,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1337935113"},{"feature_type":"variation","strand":1,"alleles":["-","C"],"end":140474023,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474024,"clinical_significance":[],"seq_region_name":"7","id":"rs1795032327"},{"seq_region_name":"7","id":"rs1214283004","clinical_significance":[],"alleles":["A","C","G","T"],"end":140474024,"strand":1,"feature_type":"variation","start":140474024,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140474026,"alleles":["AGA","A"],"strand":1,"feature_type":"variation","start":140474024,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795032558","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795032636","clinical_significance":[],"strand":1,"feature_type":"variation","end":140474030,"alleles":["AGAAAGA","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474024,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795032716","clinical_significance":[],"start":140474025,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140474024,"alleles":["-","AG","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs868449474","source":"dbSNP","start":140474025,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140474025,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795032937","source":"dbSNP","start":140474025,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["GA","GATGA"],"end":140474026,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795033013","end":140474031,"alleles":["GAAAGAA","GAAAGAAGGAAAGAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140474025,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140474026,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474026,"clinical_significance":[],"seq_region_name":"7","id":"rs1409266447"},{"start":140474026,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140474028,"alleles":["AAA","AAAA","AAAAA"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1405290743","clinical_significance":[]},{"id":"rs1263386734","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474027,"source":"dbSNP","strand":1,"feature_type":"variation","end":140474027,"alleles":["A","C","G"]},{"source":"dbSNP","start":140474028,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C","T"],"end":140474028,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1462342202"},{"end":140474030,"alleles":["AGA","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140474028,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795033566"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474029,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["-","AG"],"end":140474028,"seq_region_name":"7","id":"rs1795033655","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140474029,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474029,"source":"dbSNP","seq_region_name":"7","id":"rs866136453","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","GG"],"end":140474029,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474029,"source":"dbSNP","seq_region_name":"7","id":"rs1440944947","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474029,"source":"dbSNP","strand":1,"feature_type":"variation","end":140474029,"alleles":["G","-"],"id":"rs1563096988","seq_region_name":"7","clinical_significance":[]},{"start":140474030,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140474030,"alleles":["A","C","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1219028614","clinical_significance":[]},{"seq_region_name":"7","id":"rs1468680614","clinical_significance":[],"strand":1,"feature_type":"variation","end":140474032,"alleles":["AAA","A","AAAA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474030,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1266976171","clinical_significance":[],"start":140474030,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140474036,"alleles":["AAAGAAA","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563096989","feature_type":"variation","strand":1,"end":140474048,"alleles":["AAAGAAAGAAAGAAAGAAA","AAAGAAAGAAAGAAAGAAAAGAAAGAAAGAAAGAAA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474030},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474031,"feature_type":"variation","strand":1,"end":140474031,"alleles":["A","C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1201267954"},{"strand":1,"feature_type":"variation","alleles":["A","C","G","T"],"end":140474032,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474032,"source":"dbSNP","seq_region_name":"7","id":"rs867709003","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["AGA","A"],"end":140474034,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474032,"clinical_significance":[],"id":"rs1795034696","seq_region_name":"7"},{"id":"rs577311101","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140474033,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474033,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140474068,"alleles":["GAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAT","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474033,"source":"dbSNP","seq_region_name":"7","id":"rs1795034920","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474034,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140474034,"clinical_significance":[],"seq_region_name":"7","id":"rs1447059666"},{"alleles":["AA","AATAAAAAAA"],"end":140474035,"strand":1,"feature_type":"variation","start":140474034,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795035065","clinical_significance":[]},{"alleles":["AAA","A","AA","AAAA","AAAAA"],"end":140474036,"feature_type":"variation","strand":1,"source":"dbSNP","start":140474034,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1292001620"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474034,"source":"dbSNP","strand":1,"feature_type":"variation","end":140474036,"alleles":["AAA","-"],"seq_region_name":"7","id":"rs1563097013","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795035315","clinical_significance":[],"start":140474034,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140474040,"alleles":["AAAGAAA","AAAGAAAAAGAAA","AAAGAAAAGAAA"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1057511421","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474035,"feature_type":"variation","strand":1,"end":140474035,"alleles":["A","C","G"]},{"feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140474036,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474036,"clinical_significance":[],"seq_region_name":"7","id":"rs1195321322"},{"source":"dbSNP","start":140474036,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AGA","A"],"end":140474038,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1161860409"},{"source":"dbSNP","start":140474036,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AGAAAGA","A"],"end":140474042,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795035601"},{"start":140474036,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AGAAAGAAAGA","A"],"end":140474046,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795035654","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140474036,"alleles":["-","AG"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474037,"source":"dbSNP","id":"rs1795035712","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474037,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140474037,"seq_region_name":"7","id":"rs867128278","clinical_significance":[]},{"alleles":["G","GG"],"end":140474037,"strand":1,"feature_type":"variation","start":140474037,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795035833","clinical_significance":[]},{"alleles":["GAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAT","-"],"end":140474068,"feature_type":"variation","strand":1,"source":"dbSNP","start":140474037,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1297558097"},{"source":"dbSNP","start":140474038,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140474038,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1157586519","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1377920780","clinical_significance":[],"end":140474040,"alleles":["AAA","AA","AAAA","AAAAA"],"strand":1,"feature_type":"variation","start":140474038,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1795036110","seq_region_name":"7","source":"dbSNP","start":140474038,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AAAGAAAGAAA","A"],"end":140474048,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1563097019","seq_region_name":"7","source":"dbSNP","start":140474038,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140474067,"alleles":["AAAGAAAGAAAGAAAGAAAGAAAGAAAGAA","AAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1371199760","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474039,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140474039},{"seq_region_name":"7","id":"rs1795036308","clinical_significance":[],"strand":1,"feature_type":"variation","end":140474043,"alleles":["AAGAA","AA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474039,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474040,"source":"dbSNP","strand":1,"feature_type":"variation","end":140474040,"alleles":["A","C","T"],"id":"rs1474965758","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs75292092","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474041,"source":"dbSNP","strand":1,"feature_type":"variation","end":140474041,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1795036522","clinical_significance":[],"end":140474041,"alleles":["G","GG"],"strand":1,"feature_type":"variation","start":140474041,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140474068,"alleles":["GAAAGAAAGAAAGAAAGAAAGAAAGAAT","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140474041,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130359277"},{"clinical_significance":[],"id":"rs1218680330","seq_region_name":"7","end":140474042,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140474042,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140474042,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140474044,"alleles":["AAA","AAAA"],"strand":1,"feature_type":"variation","id":"rs1242533099","seq_region_name":"7","clinical_significance":[]},{"end":140474043,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140474043,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs917494810"},{"source":"dbSNP","start":140474043,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140474047,"alleles":["AAGAA","AA"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1430282389"},{"strand":1,"feature_type":"variation","alleles":["AGA","AGACAGA"],"end":140474046,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474044,"source":"dbSNP","seq_region_name":"7","id":"rs1795037119","clinical_significance":[]},{"id":"rs1235034153","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474045,"source":"dbSNP","strand":1,"feature_type":"variation","end":140474045,"alleles":["G","A","C","T"]},{"start":140474046,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AAA","AA","AAAA"],"end":140474048,"strand":1,"feature_type":"variation","id":"rs1795037296","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140474046,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140474052,"alleles":["AAAGAAA","AAAGAAAAGAAA"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795037366","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140474046,"alleles":["-","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474047,"clinical_significance":[],"seq_region_name":"7","id":"rs1795037436"},{"seq_region_name":"7","id":"rs949070904","clinical_significance":[],"start":140474047,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140474047,"alleles":["A","C","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1795037598","seq_region_name":"7","end":140474048,"alleles":["A","C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140474048,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795037697","clinical_significance":[],"end":140474049,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140474049,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1795037774","seq_region_name":"7","clinical_significance":[],"end":140474049,"alleles":["G","-"],"strand":1,"feature_type":"variation","start":140474049,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140474050,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474050,"source":"dbSNP","seq_region_name":"7","id":"rs2130359477","clinical_significance":[]},{"seq_region_name":"7","id":"rs1044711474","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140474051,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474051,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1398679566","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474052,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140474052},{"seq_region_name":"7","id":"rs1314035263","clinical_significance":[],"start":140474053,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140474053,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140474053,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["GAAAGAA","GAAAGAAGGAAAGAA"],"end":140474059,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795038053","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474054,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140474054,"seq_region_name":"7","id":"rs1434746100","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1382845564","feature_type":"variation","strand":1,"end":140474055,"alleles":["A","C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474055},{"seq_region_name":"7","id":"rs1795038286","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474055,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AAGAA","AA"],"end":140474059},{"seq_region_name":"7","id":"rs904949887","clinical_significance":[],"alleles":["A","G","T"],"end":140474056,"strand":1,"feature_type":"variation","start":140474056,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795038457","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["AGA","A","AGAGAGA"],"end":140474058,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474056,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140474057,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474057,"clinical_significance":[],"seq_region_name":"7","id":"rs995633767"},{"seq_region_name":"7","id":"rs1795038683","clinical_significance":[],"start":140474057,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["GAAAGAA","GAAAGAAGGAAAGAA"],"end":140474063,"strand":1,"feature_type":"variation"},{"id":"rs1320857265","seq_region_name":"7","clinical_significance":[],"end":140474068,"alleles":["GAAAGAAAGAAT","-"],"strand":1,"feature_type":"variation","start":140474057,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs145519615","clinical_significance":[],"end":140474057,"alleles":["-","GAAA"],"strand":1,"feature_type":"variation","start":140474058,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140474058,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474058,"clinical_significance":[],"seq_region_name":"7","id":"rs1795038953"},{"alleles":["AAA","AAAA"],"end":140474060,"feature_type":"variation","strand":1,"source":"dbSNP","start":140474058,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795039035"},{"seq_region_name":"7","id":"rs1795039127","clinical_significance":[],"alleles":["AAAGAAA","AAAGAAATAAAGAAA"],"end":140474064,"strand":1,"feature_type":"variation","start":140474058,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140474058,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140474072,"alleles":["AAAGAAAGAATAAAA","AA"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795039217"},{"id":"rs1325139929","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140474059,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474059,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1795039390","seq_region_name":"7","source":"dbSNP","start":140474059,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140474067,"alleles":["AAGAAAGAA","AA"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140474060,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140474060,"alleles":["A","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795039488"},{"alleles":["AGA","A"],"end":140474062,"feature_type":"variation","strand":1,"source":"dbSNP","start":140474060,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1419952417","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474061,"feature_type":"variation","strand":1,"alleles":["G","-"],"end":140474061,"clinical_significance":[],"seq_region_name":"7","id":"rs1399809705"},{"clinical_significance":[],"id":"rs1585496741","seq_region_name":"7","alleles":["G","A","T"],"end":140474061,"feature_type":"variation","strand":1,"source":"dbSNP","start":140474061,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140474062,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140474062,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1003321641","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795039994","end":140474064,"alleles":["AAA","AAAAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140474062,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["AAAGAA","AAAGAAAAAGAA"],"end":140474067,"strand":1,"feature_type":"variation","start":140474062,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795040096","clinical_significance":[]},{"seq_region_name":"7","id":"rs1326067064","clinical_significance":[],"start":140474063,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140474063,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474063,"source":"dbSNP","strand":1,"feature_type":"variation","end":140474065,"alleles":["AAG","AAGGAAG"],"seq_region_name":"7","id":"rs1795040276","clinical_significance":[]},{"seq_region_name":"7","id":"rs1284287970","clinical_significance":[],"end":140474067,"alleles":["AAGAA","AA","AAGAAAGGAAGAA"],"strand":1,"feature_type":"variation","start":140474063,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1035355374","alleles":["A","G","T"],"end":140474064,"feature_type":"variation","strand":1,"source":"dbSNP","start":140474064,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795040648","clinical_significance":[],"end":140474066,"alleles":["AGA","A"],"strand":1,"feature_type":"variation","start":140474064,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs564646288","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474065,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140474065},{"feature_type":"variation","strand":1,"end":140474067,"alleles":["GAA","GAAAGAAAGAAAGAAAGAAGGAA","GAAAGAAAGAAAGAAAGAATGAA","GAAAGAAAGAAAGAATGAA","GAAAGAAAGAATGAA","GAAAGAATGAA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474065,"clinical_significance":[],"id":"rs1563097061","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1262307670","seq_region_name":"7","end":140474068,"alleles":["GAAT","GAATGAAT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140474065,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474065,"feature_type":"variation","strand":1,"end":140474068,"alleles":["GAAT","-"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795041176"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474066,"source":"dbSNP","strand":1,"feature_type":"variation","end":140474066,"alleles":["A","G"],"id":"rs886965075","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1048242237","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474066,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AA","AAA","AAAAAA","AAAGAAAAAA","AAAGAAAGAAAAAA","AAAGAAAGAAAGAAAAAA","AAAGAAAGAAAGAAAGAAAAAA","AAAGAATAAA"],"end":140474067},{"strand":1,"feature_type":"variation","alleles":["AATAAA","AA"],"end":140474071,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474066,"source":"dbSNP","seq_region_name":"7","id":"rs1340320765","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795041651","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474066,"feature_type":"variation","strand":1,"alleles":["AATAAAA","AA"],"end":140474072},{"clinical_significance":[],"seq_region_name":"7","id":"rs1004042939","end":140474067,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140474067,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795041830","feature_type":"variation","strand":1,"end":140474067,"alleles":["A","AAGGA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474067},{"clinical_significance":[],"seq_region_name":"7","id":"rs367545500","alleles":["T","A","C","G"],"end":140474068,"feature_type":"variation","strand":1,"source":"dbSNP","start":140474068,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474068,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","-"],"end":140474068,"id":"rs1585496826","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474069,"source":"dbSNP","strand":1,"feature_type":"variation","end":140474069,"alleles":["A","G"],"seq_region_name":"7","id":"rs574505182","clinical_significance":[]},{"alleles":["AAAA","AA"],"end":140474072,"feature_type":"variation","strand":1,"source":"dbSNP","start":140474069,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1465232759"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474070,"feature_type":"variation","strand":1,"end":140474069,"alleles":["-","GAAAG"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585496859"},{"clinical_significance":[],"id":"rs1172395309","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474070,"feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140474070},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140474071,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474071,"clinical_significance":[],"id":"rs2130360162","seq_region_name":"7"},{"end":140474073,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140474073,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795042595","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474074,"source":"dbSNP","strand":1,"feature_type":"variation","end":140474074,"alleles":["A","C","G","T"],"seq_region_name":"7","id":"rs1476687731","clinical_significance":[]},{"clinical_significance":[],"id":"rs1350767986","seq_region_name":"7","feature_type":"variation","strand":1,"end":140474075,"alleles":["C","A","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474075},{"seq_region_name":"7","id":"rs1206320508","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474076,"source":"dbSNP","strand":1,"feature_type":"variation","end":140474076,"alleles":["T","A","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795043073","alleles":["G","A"],"end":140474077,"feature_type":"variation","strand":1,"source":"dbSNP","start":140474077,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["T","A","C","G"],"end":140474078,"feature_type":"variation","strand":1,"source":"dbSNP","start":140474078,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1022939541","seq_region_name":"7"},{"start":140474078,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140474078,"alleles":["T","-"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1422689580","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795043378","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140474080,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474080},{"strand":1,"feature_type":"variation","end":140474081,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474081,"source":"dbSNP","seq_region_name":"7","id":"rs1425539608","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1254155504","source":"dbSNP","start":140474082,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140474082,"feature_type":"variation","strand":1},{"end":140474083,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140474083,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795043614","seq_region_name":"7"},{"alleles":["GGG","GGGG"],"end":140474086,"strand":1,"feature_type":"variation","start":140474084,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1446314832","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795043817","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140474086,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474086},{"source":"dbSNP","start":140474087,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140474087,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1200012260","seq_region_name":"7"},{"start":140474087,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140474089,"alleles":["CCC","CCCC"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs34918735","clinical_significance":[]},{"start":140474089,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140474089,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs547962654","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795044173","clinical_significance":[],"start":140474089,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140474092,"alleles":["CGGT","CGGTCGGT"],"strand":1,"feature_type":"variation"},{"end":140474090,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140474090,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs560441295"},{"seq_region_name":"7","id":"rs996810959","clinical_significance":[],"alleles":["G","A","T"],"end":140474091,"strand":1,"feature_type":"variation","start":140474091,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["G","A","T"],"end":140474094,"feature_type":"variation","strand":1,"source":"dbSNP","start":140474094,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs781132163"},{"id":"rs1563097128","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474096,"source":"dbSNP","strand":1,"feature_type":"variation","end":140474109,"alleles":["TCACACCTACAATC","TC"]},{"end":140474099,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140474099,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1294340220","clinical_significance":[]},{"id":"rs1795044839","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140474110,"alleles":["CCTACAATCC","CC"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474101,"source":"dbSNP"},{"start":140474102,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140474102,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1247607478","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1479325274","source":"dbSNP","start":140474103,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140474104,"alleles":["TA","-"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1339292115","source":"dbSNP","start":140474105,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140474105,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795045208","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474107,"source":"dbSNP","strand":1,"feature_type":"variation","end":140474107,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs1377216321","clinical_significance":[],"alleles":["T","G"],"end":140474108,"strand":1,"feature_type":"variation","start":140474108,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140474113,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474113,"clinical_significance":[],"seq_region_name":"7","id":"rs755118277"},{"alleles":["G","-"],"end":140474113,"feature_type":"variation","strand":1,"source":"dbSNP","start":140474113,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1454386453"},{"seq_region_name":"7","id":"rs1795045535","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140474114,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474114,"source":"dbSNP"},{"end":140474114,"alleles":["-","CCA"],"strand":1,"feature_type":"variation","start":140474115,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795045580","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1160324849","clinical_significance":[],"alleles":["A","-"],"end":140474115,"strand":1,"feature_type":"variation","start":140474115,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795045643","clinical_significance":[],"start":140474115,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140474115,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474116,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140474116,"clinical_significance":[],"id":"rs1713735475","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1585497002","clinical_significance":[],"end":140474118,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140474118,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1394884121","clinical_significance":[],"end":140474121,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140474121,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795045834","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140474124,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474124},{"id":"rs1377028129","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140474125,"strand":1,"feature_type":"variation","start":140474125,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140474127,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474127,"clinical_significance":[],"seq_region_name":"7","id":"rs1795045945"},{"start":140474134,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140474134,"alleles":["G","C"],"strand":1,"feature_type":"variation","id":"rs968794537","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474135,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140474135,"seq_region_name":"7","id":"rs528759141","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140474136,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474136,"source":"dbSNP","seq_region_name":"7","id":"rs1585497034","clinical_significance":[]},{"alleles":["A","G"],"end":140474139,"feature_type":"variation","strand":1,"source":"dbSNP","start":140474139,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585497043"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474140,"source":"dbSNP","strand":1,"feature_type":"variation","end":140474140,"alleles":["T","A"],"seq_region_name":"7","id":"rs979281047","clinical_significance":[]},{"source":"dbSNP","start":140474141,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140474141,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795046317"},{"seq_region_name":"7","id":"rs1795046372","clinical_significance":[],"alleles":["A","G"],"end":140474142,"strand":1,"feature_type":"variation","start":140474142,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1585497055","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","G"],"end":140474143,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474143,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795046478","clinical_significance":[],"start":140474143,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["CC","-"],"end":140474144,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140474148,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474148,"source":"dbSNP","id":"rs1795046530","seq_region_name":"7","clinical_significance":[]},{"start":140474150,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140474150,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585497060","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140474151,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474151,"clinical_significance":[],"seq_region_name":"7","id":"rs1795046633"},{"seq_region_name":"7","id":"rs1795046687","clinical_significance":[],"start":140474154,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140474157,"alleles":["GTGT","GT"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474155,"feature_type":"variation","strand":1,"end":140474155,"alleles":["T","G"],"clinical_significance":[],"id":"rs1585497067","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474159,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140474159,"clinical_significance":[],"seq_region_name":"7","id":"rs1795046803"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474168,"feature_type":"variation","strand":1,"end":140474168,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1399249910"},{"seq_region_name":"7","id":"rs1585497076","clinical_significance":[],"start":140474170,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140474170,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474171,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140474171,"clinical_significance":[],"seq_region_name":"7","id":"rs1163684801"},{"start":140474173,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140474173,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1459378272","clinical_significance":[]},{"id":"rs1031745091","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474176,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140474176},{"id":"rs1795047094","seq_region_name":"7","clinical_significance":[],"end":140474177,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140474177,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1186769213","end":140474182,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140474182,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140474183,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140474183,"strand":1,"feature_type":"variation","id":"rs1795047209","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","T"],"end":140474187,"feature_type":"variation","strand":1,"source":"dbSNP","start":140474187,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130360898"},{"id":"rs1419708068","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474188,"source":"dbSNP","strand":1,"feature_type":"variation","end":140474188,"alleles":["C","A"]},{"alleles":["A","G"],"end":140474193,"strand":1,"feature_type":"variation","start":140474193,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1240147894","clinical_significance":[]},{"id":"rs1176976409","seq_region_name":"7","clinical_significance":[],"start":140474194,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140474194,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474198,"feature_type":"variation","strand":1,"end":140474198,"alleles":["C","A","T"],"clinical_significance":[],"id":"rs984228972","seq_region_name":"7"},{"start":140474205,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140474205,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795047503","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474212,"feature_type":"variation","strand":1,"end":140474212,"alleles":["A","C"],"clinical_significance":[],"id":"rs1457528117","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130360985","feature_type":"variation","strand":1,"alleles":["T","A"],"end":140474213,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474213},{"id":"rs1015684537","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474214,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140474214},{"seq_region_name":"7","id":"rs1211932212","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474218,"source":"dbSNP","strand":1,"feature_type":"variation","end":140474218,"alleles":["C","T"]},{"clinical_significance":[],"id":"rs2130361013","seq_region_name":"7","source":"dbSNP","start":140474219,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140474219,"alleles":["C","T"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474220,"source":"dbSNP","strand":1,"feature_type":"variation","end":140474220,"alleles":["A","C","G"],"seq_region_name":"7","id":"rs961572856","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs750515711","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140474222,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474222},{"clinical_significance":[],"seq_region_name":"7","id":"rs976914451","source":"dbSNP","start":140474223,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140474223,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1265318072","end":140474225,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140474225,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474226,"feature_type":"variation","strand":1,"end":140474226,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs767748988"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474227,"source":"dbSNP","strand":1,"feature_type":"variation","end":140474227,"alleles":["G","T"],"seq_region_name":"7","id":"rs1795048085","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140474230,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474230,"clinical_significance":[],"seq_region_name":"7","id":"rs993006896"},{"clinical_significance":[],"seq_region_name":"7","id":"rs569761314","alleles":["C","G"],"end":140474231,"feature_type":"variation","strand":1,"source":"dbSNP","start":140474231,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140474232,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140474232,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795048300","seq_region_name":"7","clinical_significance":[]},{"start":140474233,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140474233,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795048361","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130361143","end":140474236,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140474236,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1403417094","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474237,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140474237},{"start":140474238,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140474238,"strand":1,"feature_type":"variation","id":"rs1795048484","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140474245,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474245,"source":"dbSNP","seq_region_name":"7","id":"rs1795048575","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795048632","end":140474248,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140474248,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140474249,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474249,"source":"dbSNP","seq_region_name":"7","id":"rs1300177952","clinical_significance":[]},{"source":"dbSNP","start":140474258,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140474258,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1335927158","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795048792","clinical_significance":[],"end":140474261,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140474261,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795048855","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140474262,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474262},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474263,"source":"dbSNP","strand":1,"feature_type":"variation","end":140474263,"alleles":["T","C"],"seq_region_name":"7","id":"rs1444111207","clinical_significance":[]},{"seq_region_name":"7","id":"rs1375779418","clinical_significance":[],"start":140474264,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140474264,"strand":1,"feature_type":"variation"},{"end":140474265,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140474265,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs2130361254","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1323815802","clinical_significance":[],"alleles":["G","A"],"end":140474266,"strand":1,"feature_type":"variation","start":140474266,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1795049089","seq_region_name":"7","source":"dbSNP","start":140474268,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140474268,"alleles":["C","T"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474269,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140474269,"id":"rs948915519","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","A","T"],"end":140474271,"feature_type":"variation","strand":1,"source":"dbSNP","start":140474271,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs980445744","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474272,"feature_type":"variation","strand":1,"end":140474272,"alleles":["T","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585497244"},{"alleles":["G","A"],"end":140474273,"strand":1,"feature_type":"variation","start":140474273,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795049329","clinical_significance":[]},{"end":140474278,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140474278,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795049386","clinical_significance":[]},{"seq_region_name":"7","id":"rs1162552215","clinical_significance":[],"alleles":["T","A","C"],"end":140474279,"strand":1,"feature_type":"variation","start":140474279,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140474282,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474282,"source":"dbSNP","seq_region_name":"7","id":"rs2130361354","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1240594014","source":"dbSNP","start":140474283,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140474283,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs932890133","feature_type":"variation","strand":1,"end":140474288,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474288},{"clinical_significance":[],"seq_region_name":"7","id":"rs6966930","source":"dbSNP","start":140474291,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140474291,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140474292,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474292,"source":"dbSNP","seq_region_name":"7","id":"rs1795050006","clinical_significance":[]},{"id":"rs1156997668","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474298,"source":"dbSNP","strand":1,"feature_type":"variation","end":140474298,"alleles":["C","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs546120097","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474300,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140474300},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474301,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","G"],"end":140474301,"seq_region_name":"7","id":"rs1795050314","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795050447","seq_region_name":"7","end":140474305,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140474305,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474307,"source":"dbSNP","strand":1,"feature_type":"variation","end":140474307,"alleles":["C","G"],"seq_region_name":"7","id":"rs1223209897","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474313,"feature_type":"variation","strand":1,"end":140474313,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795050642"},{"clinical_significance":[],"seq_region_name":"7","id":"rs930975684","end":140474315,"alleles":["G","A","C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140474315,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["T","G"],"end":140474316,"strand":1,"feature_type":"variation","start":140474316,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1450199063","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140474322,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140474322,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1267157785"},{"source":"dbSNP","start":140474325,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140474325,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795051053"},{"start":140474326,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140474326,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs946380342","clinical_significance":[]},{"end":140474328,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140474328,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795051151","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474334,"feature_type":"variation","strand":1,"alleles":["AAAAA","AA"],"end":140474338,"clinical_significance":[],"seq_region_name":"7","id":"rs1293849055"},{"seq_region_name":"7","id":"rs1287538661","clinical_significance":[],"alleles":["C","T"],"end":140474341,"strand":1,"feature_type":"variation","start":140474341,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs148752843","seq_region_name":"7","end":140474349,"alleles":["AAAAAAAA","AAAAAAA","AAAAAAAAA","AAAAAAAAAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140474342,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140474347,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140474347,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585497337"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474347,"feature_type":"variation","strand":1,"alleles":["AAACAAACAA","AAACAA"],"end":140474356,"clinical_significance":[],"seq_region_name":"7","id":"rs1258444718"},{"id":"rs1048653816","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474348,"source":"dbSNP","strand":1,"feature_type":"variation","end":140474348,"alleles":["A","G"]},{"source":"dbSNP","start":140474349,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140474349,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs186920218","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140474351,"alleles":["ACA","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474349,"clinical_significance":[],"seq_region_name":"7","id":"rs563560734"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474350,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140474350,"seq_region_name":"7","id":"rs923656953","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474350,"source":"dbSNP","strand":1,"feature_type":"variation","end":140474350,"alleles":["C","CC"],"seq_region_name":"7","id":"rs1491223682","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795052006","feature_type":"variation","strand":1,"end":140474351,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474351},{"alleles":["T","A","C"],"end":140474357,"strand":1,"feature_type":"variation","start":140474357,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs763944720","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs939189459","feature_type":"variation","strand":1,"end":140474359,"alleles":["A","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474359},{"seq_region_name":"7","id":"rs1419116596","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474362,"source":"dbSNP","strand":1,"feature_type":"variation","end":140474362,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1425995822","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474368,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140474368},{"clinical_significance":[],"seq_region_name":"7","id":"rs532069904","feature_type":"variation","strand":1,"end":140474370,"alleles":["G","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474370},{"seq_region_name":"7","id":"rs1000190839","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140474371,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474371,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1475545043","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474374,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CACACACC","C"],"end":140474381},{"alleles":["A","G"],"end":140474377,"strand":1,"feature_type":"variation","start":140474377,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1489479437","clinical_significance":[]},{"end":140474378,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140474378,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs550666477","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140474382,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474382,"clinical_significance":[],"seq_region_name":"7","id":"rs756983765"},{"seq_region_name":"7","id":"rs1795053117","clinical_significance":[],"strand":1,"feature_type":"variation","end":140474383,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474383,"source":"dbSNP"},{"end":140474384,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140474384,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795053222"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140474388,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474388,"clinical_significance":[],"seq_region_name":"7","id":"rs895070611"},{"clinical_significance":[],"seq_region_name":"7","id":"rs780539503","source":"dbSNP","start":140474391,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140474391,"alleles":["A","G"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474394,"feature_type":"variation","strand":1,"end":140474394,"alleles":["T","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1171726063"},{"end":140474396,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140474396,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs956107605","clinical_significance":[]},{"end":140474397,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140474397,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1012197242","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140474398,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474398,"clinical_significance":[],"seq_region_name":"7","id":"rs993002429"},{"end":140474401,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140474401,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1273883605"},{"id":"rs1464333547","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474404,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140474404},{"seq_region_name":"7","id":"rs745419100","clinical_significance":[],"alleles":["T","C"],"end":140474406,"strand":1,"feature_type":"variation","start":140474406,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130361936","end":140474408,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140474408,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1403478186","clinical_significance":[],"start":140474409,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C"],"end":140474409,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140474410,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140474410,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795054296"},{"seq_region_name":"7","id":"rs1385530050","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474412,"source":"dbSNP","strand":1,"feature_type":"variation","end":140474412,"alleles":["A","ATGA"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474413,"feature_type":"variation","strand":1,"end":140474413,"alleles":["G","A"],"clinical_significance":[],"id":"rs1795054490","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474414,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140474414,"seq_region_name":"7","id":"rs1795054581","clinical_significance":[]},{"clinical_significance":[],"id":"rs1049434933","seq_region_name":"7","end":140474416,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140474416,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474418,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140474418,"id":"rs1795054770","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140474422,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474422,"clinical_significance":[],"seq_region_name":"7","id":"rs1024449710"},{"id":"rs1335583783","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474425,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140474425},{"source":"dbSNP","start":140474427,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140474427,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs191699429"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1005548635","feature_type":"variation","strand":1,"end":140474428,"alleles":["G","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474428},{"seq_region_name":"7","id":"rs1015695876","clinical_significance":[],"strand":1,"feature_type":"variation","end":140474429,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474429,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474431,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140474431,"seq_region_name":"7","id":"rs1478979475","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474432,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140474432,"seq_region_name":"7","id":"rs1342003646","clinical_significance":[]},{"alleles":["G","A","T"],"end":140474434,"strand":1,"feature_type":"variation","start":140474434,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs961430015","clinical_significance":[]},{"source":"dbSNP","start":140474435,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140474435,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1250580350"},{"start":140474436,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A","G"],"end":140474436,"strand":1,"feature_type":"variation","id":"rs1345586452","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1215356340","clinical_significance":[],"end":140474438,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140474438,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140474445,"alleles":["GGGGGGGG","GGGGGGG","GGGGGGGGG","GGGGGGGGGG"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474438,"source":"dbSNP","seq_region_name":"7","id":"rs771760476","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474439,"source":"dbSNP","strand":1,"feature_type":"variation","end":140474439,"alleles":["G","A","C","T"],"seq_region_name":"7","id":"rs375578575","clinical_significance":[]},{"clinical_significance":[],"id":"rs1276569791","seq_region_name":"7","source":"dbSNP","start":140474440,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140474440,"feature_type":"variation","strand":1},{"start":140474441,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140474441,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1441980503","clinical_significance":[]},{"start":140474443,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140474443,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1194486551","clinical_significance":[]},{"alleles":["G","A","C","T"],"end":140474444,"feature_type":"variation","strand":1,"source":"dbSNP","start":140474444,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs73489099"},{"source":"dbSNP","start":140474445,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140474445,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs140693905"},{"start":140474446,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140474446,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1476979709","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474450,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140474450,"seq_region_name":"7","id":"rs2130362263","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1029859515","source":"dbSNP","start":140474451,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140474451,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs779672763","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474452,"feature_type":"variation","strand":1,"end":140474452,"alleles":["G","A"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474453,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140474453,"clinical_significance":[],"seq_region_name":"7","id":"rs533970873"},{"source":"dbSNP","start":140474454,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140474454,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs552038196"},{"clinical_significance":[],"id":"rs760397934","seq_region_name":"7","alleles":["TT","T"],"end":140474455,"feature_type":"variation","strand":1,"source":"dbSNP","start":140474454,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1479277977","clinical_significance":[],"alleles":["T","C"],"end":140474455,"strand":1,"feature_type":"variation","start":140474455,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140474459,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474459,"source":"dbSNP","seq_region_name":"7","id":"rs1795057304","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140474461,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474461,"source":"dbSNP","seq_region_name":"7","id":"rs1795057368","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs954337144","source":"dbSNP","start":140474464,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140474464,"alleles":["C","A","G","T"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140474466,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140474466,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs920833987"},{"seq_region_name":"7","id":"rs1475962135","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140474467,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474467,"source":"dbSNP"},{"source":"dbSNP","start":140474471,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140474471,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1402122065"},{"feature_type":"variation","strand":1,"end":140474473,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474473,"clinical_significance":[],"seq_region_name":"7","id":"rs79050370"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474474,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140474474,"clinical_significance":[],"seq_region_name":"7","id":"rs1298299725"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140474476,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474476,"clinical_significance":[],"seq_region_name":"7","id":"rs537916236"},{"id":"rs1397789648","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140474479,"strand":1,"feature_type":"variation","start":140474479,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140474485,"alleles":["T","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474485,"clinical_significance":[],"id":"rs112212371","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140474487,"alleles":["C","A","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474487,"clinical_significance":[],"seq_region_name":"7","id":"rs773115826"},{"id":"rs923712528","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140474488,"strand":1,"feature_type":"variation","start":140474488,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140474489,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474489,"clinical_significance":[],"seq_region_name":"7","id":"rs1795058935"},{"seq_region_name":"7","id":"rs1272935853","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474491,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140474491},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474492,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140474492,"seq_region_name":"7","id":"rs1322120221","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795059203","seq_region_name":"7","source":"dbSNP","start":140474492,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","-"],"end":140474492,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140474493,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474493,"clinical_significance":[],"seq_region_name":"7","id":"rs75759485"},{"clinical_significance":[],"id":"rs10709936","seq_region_name":"7","feature_type":"variation","strand":1,"end":140474502,"alleles":["AAAAAAAAAA","AAAAAAAA","AAAAAAAAA","AAAAAAAAAAA","AAAAAAAAAAAA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474493},{"id":"rs1795059764","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474497,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140474497},{"source":"dbSNP","start":140474498,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140474498,"alleles":["A","C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1310152726"},{"seq_region_name":"7","id":"rs184049917","clinical_significance":[],"start":140474499,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140474499,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["AAAATAAA","AAA"],"end":140474506,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474499,"clinical_significance":[],"seq_region_name":"7","id":"rs1217375095"},{"seq_region_name":"7","id":"rs901038534","clinical_significance":[],"start":140474500,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140474499,"alleles":["-","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs759012247","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474500,"feature_type":"variation","strand":1,"alleles":["AAATAAATAAATAAA","AAATAAATAAA","AAATAAATAAATAAATAAA"],"end":140474514},{"source":"dbSNP","start":140474501,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140474501,"alleles":["A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795060322","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140474505,"alleles":["AATAA","AA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474501,"clinical_significance":[],"id":"rs1288293919","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1056606133","clinical_significance":[],"end":140474503,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140474503,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1487413364","feature_type":"variation","strand":1,"end":140474503,"alleles":["T","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474503},{"seq_region_name":"7","id":"rs1795060702","clinical_significance":[],"end":140474504,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140474504,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140474512,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140474512,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1268480347","clinical_significance":[]},{"id":"rs1435350542","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474515,"source":"dbSNP","strand":1,"feature_type":"variation","end":140474515,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs1296362945","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140474516,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474516,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1197216765","seq_region_name":"7","end":140474517,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140474517,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1377510645","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140474519,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474519,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474523,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140474523,"seq_region_name":"7","id":"rs1234055792","clinical_significance":[]},{"end":140474528,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140474528,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs916443146"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474530,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140474530,"seq_region_name":"7","id":"rs1405340542","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585497944","end":140474531,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140474531,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1440880289","source":"dbSNP","start":140474532,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140474532,"alleles":["T","C"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140474533,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474533,"clinical_significance":[],"id":"rs1795061774","seq_region_name":"7"},{"source":"dbSNP","start":140474534,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140474534,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585497956"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585497960","feature_type":"variation","strand":1,"end":140474536,"alleles":["-","AAATAAATAAATAAAA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474537},{"clinical_significance":[],"seq_region_name":"7","id":"rs904435489","source":"dbSNP","start":140474538,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C","G"],"end":140474538,"feature_type":"variation","strand":1},{"alleles":["T","-"],"end":140474538,"feature_type":"variation","strand":1,"source":"dbSNP","start":140474538,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585497972"},{"id":"rs1378039541","seq_region_name":"7","clinical_significance":[],"start":140474540,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C","T"],"end":140474540,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs947878310","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474542,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140474542},{"seq_region_name":"7","id":"rs1176291633","clinical_significance":[],"start":140474542,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140474543,"alleles":["GG","G","GGG"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474543,"feature_type":"variation","strand":1,"end":140474543,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs145915770"},{"end":140474544,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140474544,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1227725548"},{"seq_region_name":"7","id":"rs1795062835","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140474545,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474545,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795062928","end":140474546,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140474546,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["T","C"],"end":140474548,"strand":1,"feature_type":"variation","start":140474548,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130363064","clinical_significance":[]},{"source":"dbSNP","start":140474549,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140474549,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1296194643","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1795063123","seq_region_name":"7","end":140474551,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140474551,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140474552,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140474552,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1585498028","seq_region_name":"7"},{"end":140474554,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140474554,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795063295","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","A","T"],"end":140474557,"feature_type":"variation","strand":1,"source":"dbSNP","start":140474557,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs188041107"},{"end":140474558,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140474558,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1031636938","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1256421040","clinical_significance":[],"start":140474560,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140474560,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474564,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140474564,"seq_region_name":"7","id":"rs1795064437","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795064519","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["AAA","AA"],"end":140474566,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474564,"source":"dbSNP"},{"start":140474571,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TTTTT","TTT"],"end":140474575,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1318511243","clinical_significance":[]},{"start":140474577,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140474577,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795064700","clinical_significance":[]},{"seq_region_name":"7","id":"rs1457449171","clinical_significance":[],"end":140474580,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140474580,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140474587,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474587,"source":"dbSNP","id":"rs138525922","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1005559998","clinical_significance":[],"strand":1,"feature_type":"variation","end":140474588,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474588,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474593,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140474593,"clinical_significance":[],"seq_region_name":"7","id":"rs1795065117"},{"source":"dbSNP","start":140474595,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140474595,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795065194","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1292209785","source":"dbSNP","start":140474597,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140474597,"alleles":["T","C"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140474599,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474599,"clinical_significance":[],"id":"rs1795065343","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795065425","clinical_significance":[],"start":140474603,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140474603,"strand":1,"feature_type":"variation"},{"id":"rs2130363289","seq_region_name":"7","clinical_significance":[],"end":140474607,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140474607,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140474613,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474613,"source":"dbSNP","seq_region_name":"7","id":"rs1795065498","clinical_significance":[]},{"clinical_significance":[],"id":"rs1024376320","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474614,"feature_type":"variation","strand":1,"end":140474614,"alleles":["T","G"]},{"clinical_significance":[],"id":"rs1361661164","seq_region_name":"7","feature_type":"variation","strand":1,"end":140474616,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474616},{"end":140474620,"alleles":["ATTA","-"],"strand":1,"feature_type":"variation","start":140474617,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs970242157","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1001700901","alleles":["T","C"],"end":140474618,"feature_type":"variation","strand":1,"source":"dbSNP","start":140474618,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795065897","clinical_significance":[],"start":140474618,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140474624,"alleles":["TTACTTA","TTA"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs769175344","seq_region_name":"7","source":"dbSNP","start":140474621,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140474621,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1037004364","alleles":["T","G"],"end":140474622,"feature_type":"variation","strand":1,"source":"dbSNP","start":140474622,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs2130363379","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140474625,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474625},{"seq_region_name":"7","id":"rs897145642","clinical_significance":[],"start":140474630,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140474630,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140474631,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474631,"clinical_significance":[],"seq_region_name":"7","id":"rs1430678656"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474633,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140474633,"id":"rs1563097481","seq_region_name":"7","clinical_significance":[]},{"end":140474635,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140474635,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795066507","clinical_significance":[]},{"seq_region_name":"7","id":"rs1563097483","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474636,"source":"dbSNP","strand":1,"feature_type":"variation","end":140474636,"alleles":["A","T"]},{"id":"rs1292515842","seq_region_name":"7","clinical_significance":[],"end":140474638,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140474638,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs2130363442","clinical_significance":[],"alleles":["T","C"],"end":140474642,"strand":1,"feature_type":"variation","start":140474642,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs998304040","clinical_significance":[],"start":140474643,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140474643,"strand":1,"feature_type":"variation"},{"end":140474644,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140474644,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1479994623","seq_region_name":"7"},{"clinical_significance":[],"id":"rs536874043","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474656,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140474656},{"clinical_significance":[],"id":"rs1218741166","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140474657,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474657},{"source":"dbSNP","start":140474660,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140474660,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795067129"},{"seq_region_name":"7","id":"rs1470033880","clinical_significance":[],"strand":1,"feature_type":"variation","end":140474665,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474665,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795067266","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474666,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140474666},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474667,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140474667,"clinical_significance":[],"seq_region_name":"7","id":"rs1795067332"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474669,"feature_type":"variation","strand":1,"end":140474669,"alleles":["C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795067385"},{"start":140474676,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","T"],"end":140474676,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs141560777","clinical_significance":[]},{"seq_region_name":"7","id":"rs1007433401","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474677,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140474677},{"clinical_significance":[],"seq_region_name":"7","id":"rs1022503833","source":"dbSNP","start":140474683,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140474683,"feature_type":"variation","strand":1},{"start":140474685,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C","G"],"end":140474685,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs968247259","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140474686,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474686,"clinical_significance":[],"seq_region_name":"7","id":"rs1795067708"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795067760","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474686,"feature_type":"variation","strand":1,"end":140474686,"alleles":["C","-"]},{"feature_type":"variation","strand":1,"alleles":["AGATA","A"],"end":140474693,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474689,"clinical_significance":[],"seq_region_name":"7","id":"rs546175431"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1314236955","feature_type":"variation","strand":1,"end":140474690,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474690},{"seq_region_name":"7","id":"rs1795067939","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140474695,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474695,"source":"dbSNP"},{"seq_region_name":"7","id":"rs977742087","clinical_significance":[],"end":140474696,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140474696,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs961012082","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140474702,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474702},{"clinical_significance":[],"id":"rs78890773","seq_region_name":"7","source":"dbSNP","start":140474707,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140474707,"feature_type":"variation","strand":1},{"start":140474709,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140474708,"alleles":["-","GA"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1446651949","clinical_significance":[]},{"clinical_significance":[],"id":"rs1289382856","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474710,"feature_type":"variation","strand":1,"alleles":["TTTC","-"],"end":140474713},{"seq_region_name":"7","id":"rs1398740817","clinical_significance":[],"start":140474715,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140474724,"alleles":["TTCTTTCTTT","TTCTTT"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563097528","end":140474722,"alleles":["TCTTTCT","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140474716,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs960633910","feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140474717,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474717},{"alleles":["CTTTC","-"],"end":140474721,"strand":1,"feature_type":"variation","start":140474717,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1363923878","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474718,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140474718,"id":"rs1173543664","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140474718,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TTT","TT"],"end":140474720,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795068646"},{"end":140474725,"alleles":["TTTCTTTT","TTT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140474718,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1360475074"},{"end":140474719,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140474719,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795068766","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1380343198","seq_region_name":"7","end":140474720,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140474720,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["C","-"],"end":140474721,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474721,"clinical_significance":[],"id":"rs1424119389","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1476831513","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474721,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140474721},{"id":"rs1795068978","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140474722,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474722,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs10706027","feature_type":"variation","strand":1,"alleles":["TTTTTTTTTTTTTTT","TTTTTTT","TTTTTTTTTT","TTTTTTTTTTT","TTTTTTTTTTTT","TTTTTTTTTTTTT","TTTTTTTTTTTTTT","TTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTT"],"end":140474736,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474722},{"end":140474723,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140474723,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795069285","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1277368367","source":"dbSNP","start":140474725,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140474725,"alleles":["T","C"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474726,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140474726,"clinical_significance":[],"id":"rs1585498290","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140474727,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474727,"source":"dbSNP","seq_region_name":"7","id":"rs1795069500","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs991961982","alleles":["T","A"],"end":140474728,"feature_type":"variation","strand":1,"source":"dbSNP","start":140474728,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795069658","feature_type":"variation","strand":1,"alleles":["-","C"],"end":140474728,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474729},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563097567","end":140474729,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140474729,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140474732,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140474732,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs922350336"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474733,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140474733,"seq_region_name":"7","id":"rs76850745","clinical_significance":[]},{"id":"rs79207427","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474735,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140474735},{"seq_region_name":"7","id":"rs1795070090","clinical_significance":[],"strand":1,"feature_type":"variation","end":140474736,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474736,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1036574129","clinical_significance":[],"end":140474737,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140474737,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474737,"source":"dbSNP","strand":1,"feature_type":"variation","end":140474737,"alleles":["G","-"],"seq_region_name":"7","id":"rs1260448458","clinical_significance":[]},{"id":"rs1310519089","seq_region_name":"7","clinical_significance":[],"start":140474738,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140474738,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140474739,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140474739,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1326285433","seq_region_name":"7"},{"end":140474741,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140474741,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs932523688"},{"clinical_significance":[],"seq_region_name":"7","id":"rs576599539","source":"dbSNP","start":140474742,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140474742,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140474743,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474743,"clinical_significance":[],"seq_region_name":"7","id":"rs1795070591"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140474745,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474745,"clinical_significance":[],"seq_region_name":"7","id":"rs1795070669"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474749,"feature_type":"variation","strand":1,"end":140474751,"alleles":["CAC","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795070740"},{"id":"rs1795070811","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140474750,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474750,"source":"dbSNP"},{"start":140474751,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140474751,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1469010890","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140474754,"alleles":["CTCT","CT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474751,"clinical_significance":[],"id":"rs748616686","seq_region_name":"7"},{"end":140474753,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140474753,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1262981724"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795071188","source":"dbSNP","start":140474771,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A","G"],"end":140474771,"feature_type":"variation","strand":1},{"end":140474774,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140474774,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1309917720","clinical_significance":[]},{"seq_region_name":"7","id":"rs1480963187","clinical_significance":[],"end":140474776,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140474776,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140474778,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474778,"source":"dbSNP","seq_region_name":"7","id":"rs1795071775","clinical_significance":[]},{"clinical_significance":[],"id":"rs1585498409","seq_region_name":"7","feature_type":"variation","strand":1,"end":140474779,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474779},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795071944","source":"dbSNP","start":140474781,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140474781,"alleles":["C","A"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140474782,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474782,"source":"dbSNP","seq_region_name":"7","id":"rs1795072021","clinical_significance":[]},{"end":140474783,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140474783,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1201221775","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474784,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140474784,"clinical_significance":[],"id":"rs1422543035","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140474789,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474789,"source":"dbSNP","id":"rs1795072289","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474795,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140474795,"seq_region_name":"7","id":"rs925868444","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474797,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140474797,"clinical_significance":[],"seq_region_name":"7","id":"rs935902628"},{"end":140474798,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140474798,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1372375628","clinical_significance":[]},{"start":140474801,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140474801,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs1795072561","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140474802,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474802,"clinical_significance":[],"seq_region_name":"7","id":"rs1053546915"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1413430229","feature_type":"variation","strand":1,"end":140474804,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474804},{"seq_region_name":"7","id":"rs111477021","clinical_significance":[],"strand":1,"feature_type":"variation","end":140474806,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474806,"source":"dbSNP"},{"seq_region_name":"7","id":"rs947922862","clinical_significance":[],"strand":1,"feature_type":"variation","end":140474809,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474809,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs984585320","feature_type":"variation","strand":1,"end":140474813,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474813},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474820,"source":"dbSNP","strand":1,"feature_type":"variation","end":140474820,"alleles":["G","C"],"id":"rs1795073145","seq_region_name":"7","clinical_significance":[]},{"end":140474826,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140474826,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795073236","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795073316","clinical_significance":[],"start":140474826,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","CC"],"end":140474826,"strand":1,"feature_type":"variation"},{"alleles":["A","C"],"end":140474831,"feature_type":"variation","strand":1,"source":"dbSNP","start":140474831,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1585498476","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795073467","clinical_significance":[],"start":140474832,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140474832,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1183202201","source":"dbSNP","start":140474835,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140474835,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1458429927","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474838,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140474838},{"clinical_significance":[],"seq_region_name":"7","id":"rs1240409826","feature_type":"variation","strand":1,"alleles":["A","AA"],"end":140474843,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474843},{"clinical_significance":[],"id":"rs1045882986","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140474845,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474845},{"source":"dbSNP","start":140474847,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140474847,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795073925"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474848,"source":"dbSNP","strand":1,"feature_type":"variation","end":140474848,"alleles":["G","A"],"seq_region_name":"7","id":"rs558686580","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795074132","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140474853,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474853},{"strand":1,"feature_type":"variation","end":140474857,"alleles":["GGATT","GGATTGGATT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474853,"source":"dbSNP","id":"rs1795074209","seq_region_name":"7","clinical_significance":[]},{"end":140474855,"alleles":["A","G","T"],"strand":1,"feature_type":"variation","start":140474855,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs902067157","clinical_significance":[]},{"id":"rs1266507936","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140474862,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474862,"source":"dbSNP"},{"source":"dbSNP","start":140474864,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140474864,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795074435"},{"alleles":["C","A","T"],"end":140474867,"feature_type":"variation","strand":1,"source":"dbSNP","start":140474867,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1451601359"},{"alleles":["G","A","C"],"end":140474868,"feature_type":"variation","strand":1,"source":"dbSNP","start":140474868,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs940615466"},{"seq_region_name":"7","id":"rs1322972252","clinical_significance":[],"strand":1,"feature_type":"variation","end":140474871,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474871,"source":"dbSNP"},{"id":"rs193018219","seq_region_name":"7","clinical_significance":[],"end":140474872,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140474872,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs185357155","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474873,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140474873},{"feature_type":"variation","strand":1,"end":140474875,"alleles":["C","A","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474875,"clinical_significance":[],"seq_region_name":"7","id":"rs1377102178"},{"source":"dbSNP","start":140474876,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140474876,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs190603494"},{"strand":1,"feature_type":"variation","end":140474877,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474877,"source":"dbSNP","seq_region_name":"7","id":"rs527548907","clinical_significance":[]},{"seq_region_name":"7","id":"rs1005159284","clinical_significance":[],"alleles":["G","A"],"end":140474881,"strand":1,"feature_type":"variation","start":140474881,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140474891,"alleles":["G","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474891,"clinical_significance":[],"seq_region_name":"7","id":"rs1395550504"},{"end":140474892,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140474892,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1294008924","clinical_significance":[]},{"start":140474896,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140474896,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1015580803","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140474898,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474898,"source":"dbSNP","seq_region_name":"7","id":"rs552458927","clinical_significance":[]},{"id":"rs137964584","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474900,"source":"dbSNP","strand":1,"feature_type":"variation","end":140474900,"alleles":["G","A"]},{"id":"rs1218754266","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140474908,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474908,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1285096152","clinical_significance":[],"start":140474909,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140474909,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"start":140474910,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140474910,"alleles":["G","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1382349527","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140474911,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474911,"source":"dbSNP","seq_region_name":"7","id":"rs1177037814","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474912,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140474912,"clinical_significance":[],"seq_region_name":"7","id":"rs7779827"},{"strand":1,"feature_type":"variation","alleles":["TTT","TTTTT"],"end":140474914,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474912,"source":"dbSNP","seq_region_name":"7","id":"rs1437577168","clinical_significance":[]},{"seq_region_name":"7","id":"rs1212135229","clinical_significance":[],"start":140474915,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140474915,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795075908","source":"dbSNP","start":140474916,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140474916,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130364801","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140474920,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474920},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474921,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140474921,"clinical_significance":[],"id":"rs549845792","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1291693074","seq_region_name":"7","source":"dbSNP","start":140474922,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140474922,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474925,"feature_type":"variation","strand":1,"end":140474925,"alleles":["G","A"],"clinical_significance":[],"id":"rs182263426","seq_region_name":"7"},{"id":"rs1022392709","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474926,"source":"dbSNP","strand":1,"feature_type":"variation","end":140474926,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1795076781","clinical_significance":[],"start":140474927,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140474927,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474931,"feature_type":"variation","strand":1,"end":140474931,"alleles":["C","A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs183563917"},{"seq_region_name":"7","id":"rs1795076920","clinical_significance":[],"start":140474933,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140474933,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"id":"rs2130364881","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140474935,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474935,"source":"dbSNP"},{"start":140474938,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140474938,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1201974441","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs535453781","source":"dbSNP","start":140474939,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140474939,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1310952399","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474939,"feature_type":"variation","strand":1,"alleles":["G","GG"],"end":140474939},{"source":"dbSNP","start":140474940,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140474940,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795077051","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140474944,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474944,"clinical_significance":[],"id":"rs1795077116","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1388443401","clinical_significance":[],"start":140474945,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140474945,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"end":140474956,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140474956,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs770608961","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474957,"source":"dbSNP","strand":1,"feature_type":"variation","end":140474957,"alleles":["G","T"],"seq_region_name":"7","id":"rs1795077265","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140474958,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474958,"source":"dbSNP","seq_region_name":"7","id":"rs1795077312","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474959,"feature_type":"variation","strand":1,"end":140474959,"alleles":["T","C"],"clinical_significance":[],"id":"rs1363567450","seq_region_name":"7"},{"alleles":["C","T"],"end":140474964,"strand":1,"feature_type":"variation","start":140474964,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1302495871","clinical_significance":[]},{"start":140474965,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140474965,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs188050998","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795077533","clinical_significance":[],"alleles":["T","-"],"end":140474965,"strand":1,"feature_type":"variation","start":140474965,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1362581367","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140474970,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474970},{"source":"dbSNP","start":140474971,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140474971,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795078249"},{"start":140474972,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140474972,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs572124124","clinical_significance":[]},{"source":"dbSNP","start":140474978,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140474978,"alleles":["C","A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1177400707"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1053070434","feature_type":"variation","strand":1,"end":140474979,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474979},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140474980,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140474980,"clinical_significance":[],"seq_region_name":"7","id":"rs1201374544"},{"id":"rs913132952","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474982,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140474982},{"clinical_significance":[],"seq_region_name":"7","id":"rs1268742763","source":"dbSNP","start":140474985,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140474985,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs539717327","clinical_significance":[],"start":140474987,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140474987,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"id":"rs112122053","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474988,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140474988},{"seq_region_name":"7","id":"rs1287603152","clinical_significance":[],"strand":1,"feature_type":"variation","end":140474992,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140474992,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795078787","feature_type":"variation","strand":1,"end":140475000,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475000},{"clinical_significance":[],"id":"rs1202990400","seq_region_name":"7","source":"dbSNP","start":140475001,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140475004,"alleles":["GAGA","GAGAGA"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130365183","source":"dbSNP","start":140475003,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140475003,"alleles":["G","A"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475005,"feature_type":"variation","strand":1,"end":140475005,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1023388041"},{"start":140475007,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140475007,"alleles":["C","A","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs905961209","clinical_significance":[]},{"end":140475008,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140475008,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1343440315"},{"alleles":["C","T"],"end":140475010,"strand":1,"feature_type":"variation","start":140475010,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1282525693","clinical_significance":[]},{"seq_region_name":"7","id":"rs7790232","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475011,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140475011},{"clinical_significance":[],"id":"rs984524759","seq_region_name":"7","alleles":["C","T"],"end":140475014,"feature_type":"variation","strand":1,"source":"dbSNP","start":140475014,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs763323081","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475017,"feature_type":"variation","strand":1,"end":140475017,"alleles":["C","G"]},{"alleles":["CTGATCT","CT"],"end":140475023,"feature_type":"variation","strand":1,"source":"dbSNP","start":140475017,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795079394"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1400194952","feature_type":"variation","strand":1,"alleles":["-","A"],"end":140475018,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475019},{"start":140475019,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C","T"],"end":140475019,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1403105182","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795079572","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","T"],"end":140475020,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475020},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795079632","end":140475025,"alleles":["TCTTT","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140475021,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140475022,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["-","A"],"end":140475021,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1468530325"},{"seq_region_name":"7","id":"rs1429079882","clinical_significance":[],"alleles":["TTT","TTTTT"],"end":140475025,"strand":1,"feature_type":"variation","start":140475023,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795079798","source":"dbSNP","start":140475025,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140475025,"alleles":["T","C"],"feature_type":"variation","strand":1},{"start":140475027,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140475027,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795079850","clinical_significance":[]},{"alleles":["G","A"],"end":140475028,"strand":1,"feature_type":"variation","start":140475028,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs940500879","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475028,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GT","-"],"end":140475029,"seq_region_name":"7","id":"rs1795079969","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475032,"feature_type":"variation","strand":1,"end":140475032,"alleles":["C","A","G","T"],"clinical_significance":[],"id":"rs140548381","seq_region_name":"7"},{"source":"dbSNP","start":140475033,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140475033,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs117323193"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1243341624","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475038,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140475038},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140475042,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475042,"clinical_significance":[],"seq_region_name":"7","id":"rs1349061194"},{"clinical_significance":[],"seq_region_name":"7","id":"rs574536064","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475043,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140475043},{"seq_region_name":"7","id":"rs774764855","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475044,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140475044},{"clinical_significance":[],"seq_region_name":"7","id":"rs1015217544","alleles":["A","G","T"],"end":140475048,"feature_type":"variation","strand":1,"source":"dbSNP","start":140475048,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140475061,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475061,"clinical_significance":[],"seq_region_name":"7","id":"rs1795080573"},{"seq_region_name":"7","id":"rs759922530","clinical_significance":[],"start":140475069,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","T"],"end":140475069,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs889889556","seq_region_name":"7","feature_type":"variation","strand":1,"end":140475070,"alleles":["G","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475070},{"start":140475070,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["GGGGG","GGGGGGG"],"end":140475074,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs902062483","clinical_significance":[]},{"source":"dbSNP","start":140475074,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140475074,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795080838"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475077,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CATGCCTGTAATCCCA","CATGCCTGTAATCCCACATGCCTGTAATCCCA"],"end":140475092,"seq_region_name":"7","id":"rs1795080918","clinical_significance":[]},{"seq_region_name":"7","id":"rs180914251","clinical_significance":[],"end":140475078,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140475078,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1795081026","seq_region_name":"7","clinical_significance":[],"end":140475088,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140475088,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795081092","clinical_significance":[],"start":140475093,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140475093,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140475096,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475096,"clinical_significance":[],"seq_region_name":"7","id":"rs560153695"},{"end":140475099,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140475099,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs111559619","clinical_significance":[]},{"seq_region_name":"7","id":"rs1309193231","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475100,"source":"dbSNP","strand":1,"feature_type":"variation","end":140475100,"alleles":["G","A"]},{"end":140475102,"alleles":["GGG","GGGG"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140475100,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795081871"},{"id":"rs1795081927","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140475102,"strand":1,"feature_type":"variation","start":140475102,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795081987","clinical_significance":[],"strand":1,"feature_type":"variation","end":140475104,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475104,"source":"dbSNP"},{"start":140475108,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AA","A"],"end":140475109,"strand":1,"feature_type":"variation","id":"rs1430045100","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1360742314","seq_region_name":"7","feature_type":"variation","strand":1,"end":140475110,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475110},{"clinical_significance":[],"id":"rs1795082167","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475111,"feature_type":"variation","strand":1,"end":140475111,"alleles":["G","A"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475115,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140475115,"clinical_significance":[],"id":"rs1341179970","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795082277","end":140475118,"alleles":["GG","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140475117,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140475121,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140475121,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795082344"},{"source":"dbSNP","start":140475123,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140475123,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1225325114"},{"clinical_significance":[],"seq_region_name":"7","id":"rs999641041","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475124,"feature_type":"variation","strand":1,"end":140475124,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795082547","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475125,"feature_type":"variation","strand":1,"end":140475125,"alleles":["T","A"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475126,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140475126,"seq_region_name":"7","id":"rs1450794034","clinical_significance":[]},{"id":"rs985249970","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140475128,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475128,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1031222981","source":"dbSNP","start":140475130,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140475130,"alleles":["T","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1405793002","source":"dbSNP","start":140475132,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140475132,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140475134,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140475134,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1171915976"},{"clinical_significance":[],"seq_region_name":"7","id":"rs896693986","alleles":["G","C"],"end":140475136,"feature_type":"variation","strand":1,"source":"dbSNP","start":140475136,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585499045","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475137,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140475137},{"clinical_significance":[],"id":"rs1013272180","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475139,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140475139},{"alleles":["A","C","G"],"end":140475143,"strand":1,"feature_type":"variation","start":140475143,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1023695137","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475147,"feature_type":"variation","strand":1,"end":140475147,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795083149"},{"seq_region_name":"7","id":"rs1451377917","clinical_significance":[],"start":140475148,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140475148,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1795083265","clinical_significance":[],"start":140475149,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140475149,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140475150,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475150,"source":"dbSNP","seq_region_name":"7","id":"rs536622088","clinical_significance":[]},{"start":140475151,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140475151,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130365877","clinical_significance":[]},{"clinical_significance":[],"id":"rs541779598","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140475152,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475152},{"start":140475158,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140475158,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795083460","clinical_significance":[]},{"clinical_significance":[],"id":"rs1234187987","seq_region_name":"7","source":"dbSNP","start":140475159,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C","G"],"end":140475159,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140475160,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475160,"clinical_significance":[],"seq_region_name":"7","id":"rs1795083622"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795083682","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475161,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140475161},{"source":"dbSNP","start":140475163,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140475163,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1563097784","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140475163,"alleles":["G","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475163,"source":"dbSNP","seq_region_name":"7","id":"rs1795083801","clinical_significance":[]},{"start":140475166,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140475166,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585499099","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475170,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140475170,"seq_region_name":"7","id":"rs1795083936","clinical_significance":[]},{"end":140475171,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140475171,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795083992","clinical_significance":[]},{"end":140475172,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140475172,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1417923743","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1585499106","seq_region_name":"7","end":140475173,"alleles":["-","ATT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140475174,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140475178,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140475178,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130366023"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475179,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140475179,"seq_region_name":"7","id":"rs2130366044","clinical_significance":[]},{"start":140475183,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140475183,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1006011714","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs558148463","end":140475184,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140475184,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs2130366079","clinical_significance":[],"end":140475187,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140475187,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs961881551","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140475190,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475190,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1287989605","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140475191,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475191},{"id":"rs1795085048","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475191,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","TT"],"end":140475191},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795085099","alleles":["G","C"],"end":140475197,"feature_type":"variation","strand":1,"source":"dbSNP","start":140475197,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140475199,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140475199,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs372671101"},{"seq_region_name":"7","id":"rs531395744","clinical_significance":[],"alleles":["G","A"],"end":140475200,"strand":1,"feature_type":"variation","start":140475200,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140475205,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140475205,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795085313"},{"id":"rs1198975387","seq_region_name":"7","clinical_significance":[],"start":140475206,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140475206,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1370111224","feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140475208,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475208},{"clinical_significance":[],"seq_region_name":"7","id":"rs71171000","feature_type":"variation","strand":1,"end":140475234,"alleles":["TGGCACGTGCCTGTAATCCCAGCTTCT","TGGCACGTGCCTGTAATCCCAGCTTCTGGCACGTGCCTGTAATCCCAGCTTCT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475208},{"end":140475212,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140475212,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1240838378"},{"alleles":["C","A","T"],"end":140475213,"strand":1,"feature_type":"variation","start":140475213,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs923231482","clinical_significance":[]},{"seq_region_name":"7","id":"rs117861379","clinical_significance":[],"strand":1,"feature_type":"variation","end":140475214,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475214,"source":"dbSNP"},{"alleles":["TGCCTGTAAT","T"],"end":140475224,"strand":1,"feature_type":"variation","start":140475215,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1213958810","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1351675390","clinical_significance":[],"end":140475217,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140475217,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140475218,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140475218,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1238599167","clinical_significance":[]},{"clinical_significance":[],"id":"rs1286090941","seq_region_name":"7","source":"dbSNP","start":140475225,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140475225,"alleles":["C","A","G","T"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475229,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140475229,"seq_region_name":"7","id":"rs1382223962","clinical_significance":[]},{"id":"rs1244050821","seq_region_name":"7","clinical_significance":[],"end":140475243,"alleles":["GCTTCTCGGAAGGCT","GCT"],"strand":1,"feature_type":"variation","start":140475229,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140475232,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475232,"source":"dbSNP","seq_region_name":"7","id":"rs1795086118","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140475234,"alleles":["T","TGGCACGTGCCTGTAAT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475234,"clinical_significance":[],"seq_region_name":"7","id":"rs753187323"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475235,"feature_type":"variation","strand":1,"end":140475234,"alleles":["-","GGCACGTGC"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585499230"},{"seq_region_name":"7","id":"rs1266198456","clinical_significance":[],"strand":1,"feature_type":"variation","end":140475235,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475235,"source":"dbSNP"},{"clinical_significance":[],"id":"rs759006970","seq_region_name":"7","end":140475245,"alleles":["CGGAAGGCTGA","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140475235,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475236,"feature_type":"variation","strand":1,"end":140475236,"alleles":["G","A"],"clinical_significance":[],"id":"rs10262721","seq_region_name":"7"},{"alleles":["G","A","C"],"end":140475237,"strand":1,"feature_type":"variation","start":140475237,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1208390872","clinical_significance":[]},{"start":140475239,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140475239,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1252807064","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475240,"feature_type":"variation","strand":1,"end":140475240,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs911237769"},{"feature_type":"variation","strand":1,"end":140475240,"alleles":["-","TGCCTGTAATCCCA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475241,"clinical_significance":[],"id":"rs1458585788","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1181115064","seq_region_name":"7","feature_type":"variation","strand":1,"end":140475242,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475242},{"seq_region_name":"7","id":"rs1795086873","clinical_significance":[],"start":140475243,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140475243,"strand":1,"feature_type":"variation"},{"start":140475244,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140475244,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795086932","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475248,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140475248,"id":"rs1239460154","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795087055","clinical_significance":[],"start":140475249,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140475249,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"id":"rs942701976","seq_region_name":"7","clinical_significance":[],"start":140475250,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140475250,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"id":"rs1157754801","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140475251,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475251,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs751414816","source":"dbSNP","start":140475252,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G","T"],"end":140475252,"feature_type":"variation","strand":1},{"start":140475253,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140475253,"strand":1,"feature_type":"variation","id":"rs1795087306","seq_region_name":"7","clinical_significance":[]},{"start":140475256,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140475256,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1459153592","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795087427","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140475259,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475259},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140475266,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475266,"clinical_significance":[],"seq_region_name":"7","id":"rs1161214943"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1182071812","source":"dbSNP","start":140475269,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140475269,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140475273,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475273,"clinical_significance":[],"seq_region_name":"7","id":"rs11769245"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475280,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140475280,"seq_region_name":"7","id":"rs1447410100","clinical_significance":[]},{"seq_region_name":"7","id":"rs1442250714","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475281,"source":"dbSNP","strand":1,"feature_type":"variation","end":140475281,"alleles":["T","G"]},{"feature_type":"variation","strand":1,"end":140475286,"alleles":["GTAGT","GT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475282,"clinical_significance":[],"seq_region_name":"7","id":"rs1795087795"},{"seq_region_name":"7","id":"rs1333362392","clinical_significance":[],"start":140475283,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140475283,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1422406574","clinical_significance":[],"strand":1,"feature_type":"variation","end":140475285,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475285,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140475287,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475287,"clinical_significance":[],"seq_region_name":"7","id":"rs1384164612"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140475289,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475289,"source":"dbSNP","id":"rs1374579773","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795088105","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475289,"source":"dbSNP","strand":1,"feature_type":"variation","end":140475302,"alleles":["GCCGAGATCGTGCC","GCC"]},{"seq_region_name":"7","id":"rs1390842397","clinical_significance":[],"strand":1,"feature_type":"variation","end":140475291,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475291,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1043823771","clinical_significance":[],"strand":1,"feature_type":"variation","end":140475292,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475292,"source":"dbSNP"},{"start":140475293,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140475293,"alleles":["A","G"],"strand":1,"feature_type":"variation","id":"rs1795088381","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140475294,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475294,"source":"dbSNP","seq_region_name":"7","id":"rs1481476298","clinical_significance":[]},{"seq_region_name":"7","id":"rs575665028","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475295,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140475295},{"end":140475297,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140475297,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1242939816","clinical_significance":[]},{"alleles":["CG","-"],"end":140475298,"feature_type":"variation","strand":1,"source":"dbSNP","start":140475297,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1323693946"},{"start":140475298,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140475298,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1272929958","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1319115718","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475299,"feature_type":"variation","strand":1,"end":140475299,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs10274673","end":140475301,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140475301,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140475301,"alleles":["C","CAC"],"strand":1,"feature_type":"variation","start":140475301,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1200919237","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1293865083","alleles":["T","C"],"end":140475305,"feature_type":"variation","strand":1,"source":"dbSNP","start":140475305,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1480605930","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475307,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140475307},{"seq_region_name":"7","id":"rs1176085299","clinical_significance":[],"start":140475308,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140475308,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140475312,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475312,"source":"dbSNP","seq_region_name":"7","id":"rs935506863","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1358847966","feature_type":"variation","strand":1,"alleles":["G","GG"],"end":140475314,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475314},{"strand":1,"feature_type":"variation","end":140475316,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475316,"source":"dbSNP","seq_region_name":"7","id":"rs1256297728","clinical_significance":[]},{"clinical_significance":[],"id":"rs570653241","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475318,"feature_type":"variation","strand":1,"alleles":["GGG","GGGG"],"end":140475320},{"source":"dbSNP","start":140475321,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140475321,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs749849007","seq_region_name":"7"},{"source":"dbSNP","start":140475322,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140475322,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1053010732","seq_region_name":"7"},{"id":"rs751905767","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475323,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["ACACA","ACA"],"end":140475327},{"source":"dbSNP","start":140475325,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140475325,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs896748994"},{"clinical_significance":[],"id":"rs1049181224","seq_region_name":"7","end":140475326,"alleles":["C","CC"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140475326,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1465888235","clinical_significance":[],"start":140475326,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G","T"],"end":140475326,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475330,"source":"dbSNP","strand":1,"feature_type":"variation","end":140475330,"alleles":["C","T"],"seq_region_name":"7","id":"rs1422169535","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475331,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140475331,"id":"rs1014276143","seq_region_name":"7","clinical_significance":[]},{"id":"rs1172582684","seq_region_name":"7","clinical_significance":[],"start":140475334,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140475334,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"alleles":["T","A"],"end":140475335,"feature_type":"variation","strand":1,"source":"dbSNP","start":140475335,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1397971400"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140475338,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475338,"source":"dbSNP","seq_region_name":"7","id":"rs1461453554","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130367022","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475339,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140475339},{"seq_region_name":"7","id":"rs1795090465","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["AGAAAA","A"],"end":140475344,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475339,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140475340,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475340,"clinical_significance":[],"id":"rs547508779","seq_region_name":"7"},{"source":"dbSNP","start":140475341,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140475344,"alleles":["AAAA","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs755492635","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475341,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AAAACAAA","AAA"],"end":140475348,"seq_region_name":"7","id":"rs2130367056","clinical_significance":[]},{"seq_region_name":"7","id":"rs139052285","clinical_significance":[],"alleles":["AAACAAACAAACAAACAAACAAA","AAACAAACAAA","AAACAAACAAACAAA","AAACAAACAAACAAACAAA","AAACAAACAAACAAACAAACAAACAAA"],"end":140475364,"strand":1,"feature_type":"variation","start":140475342,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585499579","feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140475345,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475345},{"source":"dbSNP","start":140475346,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140475346,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1478241613"},{"alleles":["C","G","T"],"end":140475349,"strand":1,"feature_type":"variation","start":140475349,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs565914950","clinical_significance":[]},{"source":"dbSNP","start":140475349,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","CC"],"end":140475349,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795091050","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475350,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140475350,"clinical_significance":[],"seq_region_name":"7","id":"rs940874960"},{"id":"rs1795091175","seq_region_name":"7","clinical_significance":[],"end":140475357,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140475357,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs904891019","clinical_significance":[],"end":140475360,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140475360,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475362,"source":"dbSNP","strand":1,"feature_type":"variation","end":140475365,"alleles":["AAAA","-"],"id":"rs2130367190","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","T"],"end":140475371,"strand":1,"feature_type":"variation","start":140475371,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795091307","clinical_significance":[]},{"id":"rs1490200125","seq_region_name":"7","clinical_significance":[],"end":140475378,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140475378,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1036901297","seq_region_name":"7","alleles":["C","T"],"end":140475380,"feature_type":"variation","strand":1,"source":"dbSNP","start":140475380,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475381,"feature_type":"variation","strand":1,"end":140475381,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1394044589"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1292828792","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475383,"feature_type":"variation","strand":1,"end":140475383,"alleles":["A","G"]},{"id":"rs1005854163","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140475384,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475384,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795091666","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475385,"feature_type":"variation","strand":1,"end":140475384,"alleles":["-","TT"]},{"start":140475387,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140475387,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795091724","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795091773","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475389,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140475389},{"seq_region_name":"7","id":"rs564733383","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140475391,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475391,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475395,"source":"dbSNP","strand":1,"feature_type":"variation","end":140475395,"alleles":["C","A","T"],"seq_region_name":"7","id":"rs1795091913","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140475399,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475399,"clinical_significance":[],"seq_region_name":"7","id":"rs1795091979"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1220125810","end":140475402,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140475402,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["TC","TCTC"],"end":140475407,"feature_type":"variation","strand":1,"source":"dbSNP","start":140475406,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795092089"},{"feature_type":"variation","strand":1,"end":140475407,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475407,"clinical_significance":[],"seq_region_name":"7","id":"rs1795092167"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795092216","feature_type":"variation","strand":1,"end":140475414,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475414},{"clinical_significance":[],"id":"rs2130367368","seq_region_name":"7","source":"dbSNP","start":140475415,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140475415,"alleles":["T","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563097953","feature_type":"variation","strand":1,"end":140475418,"alleles":["A","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475418},{"clinical_significance":[],"seq_region_name":"7","id":"rs1347812465","feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140475419,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475419},{"alleles":["C","A","G","T"],"end":140475425,"feature_type":"variation","strand":1,"source":"dbSNP","start":140475425,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1029180675"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475426,"source":"dbSNP","strand":1,"feature_type":"variation","end":140475426,"alleles":["G","A"],"seq_region_name":"7","id":"rs1475627716","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475428,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140475428,"clinical_significance":[],"seq_region_name":"7","id":"rs1585499686"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140475430,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475430,"source":"dbSNP","id":"rs1344311287","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140475431,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475431,"clinical_significance":[],"seq_region_name":"7","id":"rs889477962"},{"end":140475432,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140475432,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795092745","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1006958978","source":"dbSNP","start":140475433,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140475433,"feature_type":"variation","strand":1},{"start":140475434,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140475434,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585499717","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795092951","clinical_significance":[],"start":140475436,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AAA","AAAA"],"end":140475438,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140475439,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475439,"clinical_significance":[],"seq_region_name":"7","id":"rs1795093014"},{"source":"dbSNP","start":140475443,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140475443,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs780015373","seq_region_name":"7"},{"source":"dbSNP","start":140475447,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140475447,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs539857697"},{"end":140475449,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140475449,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795093187","clinical_significance":[]},{"seq_region_name":"7","id":"rs751505483","clinical_significance":[],"start":140475451,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140475451,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1326724721","clinical_significance":[],"start":140475452,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140475452,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1585499746","clinical_significance":[],"alleles":["T","G"],"end":140475455,"strand":1,"feature_type":"variation","start":140475455,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140475461,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475461,"clinical_significance":[],"seq_region_name":"7","id":"rs1170219681"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795093516","source":"dbSNP","start":140475464,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140475464,"alleles":["A","G"],"feature_type":"variation","strand":1},{"id":"rs1795093564","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475465,"source":"dbSNP","strand":1,"feature_type":"variation","end":140475490,"alleles":["GCCTAGGCAACAGGGTGAAACCCTGT","GCCTAGGCAACAGGGTGAAACCCTGTGCCTAGGCAACAGGGTGAAACCCTGT"]},{"seq_region_name":"7","id":"rs1431223956","clinical_significance":[],"start":140475466,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140475466,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475467,"source":"dbSNP","strand":1,"feature_type":"variation","end":140475467,"alleles":["C","T"],"seq_region_name":"7","id":"rs1197171964","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475469,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140475469,"seq_region_name":"7","id":"rs1795093740","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475470,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140475470,"seq_region_name":"7","id":"rs1795093797","clinical_significance":[]},{"end":140475471,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140475471,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795093881","clinical_significance":[]},{"seq_region_name":"7","id":"rs1480106958","clinical_significance":[],"end":140475472,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140475472,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475473,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140475473,"clinical_significance":[],"seq_region_name":"7","id":"rs1795094004"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475479,"source":"dbSNP","strand":1,"feature_type":"variation","end":140475479,"alleles":["G","A"],"seq_region_name":"7","id":"rs1263819207","clinical_significance":[]},{"id":"rs1795094126","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140475480,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475480,"source":"dbSNP"},{"source":"dbSNP","start":140475485,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140475485,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs139858841"},{"source":"dbSNP","start":140475489,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140475489,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1397790139"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475496,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140475496,"seq_region_name":"7","id":"rs957314726","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs954551442","end":140475504,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140475504,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140475505,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140475505,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795094432"},{"id":"rs988675959","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["AAAAAAAAA","AAAAAAAA","AAAAAAAAAA"],"end":140475514,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475506,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795094608","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140475511,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475511},{"clinical_significance":[],"seq_region_name":"7","id":"rs1326079265","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475512,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140475512},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795094744","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475514,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140475514},{"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140475515,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475515,"clinical_significance":[],"seq_region_name":"7","id":"rs1795094827"},{"clinical_significance":[],"seq_region_name":"7","id":"rs971202807","feature_type":"variation","strand":1,"alleles":["TT","T"],"end":140475516,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475515},{"clinical_significance":[],"seq_region_name":"7","id":"rs986493337","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140475516,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475516},{"seq_region_name":"7","id":"rs1795095471","clinical_significance":[],"start":140475517,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140475517,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140475518,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140475518,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1563098009"},{"alleles":["G","T"],"end":140475524,"strand":1,"feature_type":"variation","start":140475524,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795095652","clinical_significance":[]},{"alleles":["G","T"],"end":140475525,"strand":1,"feature_type":"variation","start":140475525,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1223438974","seq_region_name":"7","clinical_significance":[]},{"start":140475527,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["GG","GGG"],"end":140475528,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795095770","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140475528,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475528,"source":"dbSNP","id":"rs1795095834","seq_region_name":"7","clinical_significance":[]},{"end":140475529,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140475529,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs2130367922","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140475530,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475530,"source":"dbSNP","id":"rs12537434","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140475531,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475531,"source":"dbSNP","seq_region_name":"7","id":"rs185318829","clinical_significance":[]},{"seq_region_name":"7","id":"rs1298391841","clinical_significance":[],"start":140475532,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140475532,"strand":1,"feature_type":"variation"},{"start":140475534,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G","T"],"end":140475534,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs781135848","clinical_significance":[]},{"clinical_significance":[],"id":"rs979365110","seq_region_name":"7","source":"dbSNP","start":140475535,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140475535,"feature_type":"variation","strand":1},{"alleles":["C","A"],"end":140475538,"feature_type":"variation","strand":1,"source":"dbSNP","start":140475538,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795096277","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475539,"source":"dbSNP","strand":1,"feature_type":"variation","end":140475539,"alleles":["C","T"],"seq_region_name":"7","id":"rs925390930","clinical_significance":[]},{"clinical_significance":[],"id":"rs1173904233","seq_region_name":"7","end":140475541,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140475541,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1791955615","clinical_significance":[],"start":140475549,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140475549,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140475556,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140475559,"alleles":["GGGG","GGG"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1217703443"},{"clinical_significance":[],"id":"rs1795096444","seq_region_name":"7","alleles":["G","A"],"end":140475559,"feature_type":"variation","strand":1,"source":"dbSNP","start":140475559,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs111671771","clinical_significance":[],"start":140475562,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140475562,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140475563,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475563,"clinical_significance":[],"seq_region_name":"7","id":"rs1052519341"},{"feature_type":"variation","strand":1,"end":140475566,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475566,"clinical_significance":[],"seq_region_name":"7","id":"rs570375625"},{"seq_region_name":"7","id":"rs1795096718","clinical_significance":[],"start":140475568,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140475568,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475571,"feature_type":"variation","strand":1,"end":140475571,"alleles":["G","A"],"clinical_significance":[],"id":"rs918117572","seq_region_name":"7"},{"end":140475572,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140475572,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1325081886","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1172481347","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140475573,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475573,"source":"dbSNP"},{"id":"rs574297085","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475574,"source":"dbSNP","strand":1,"feature_type":"variation","end":140475574,"alleles":["G","A","C"]},{"seq_region_name":"7","id":"rs1795097026","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475575,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140475575},{"start":140475576,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140475576,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs909304050","clinical_significance":[]},{"seq_region_name":"7","id":"rs1261186295","clinical_significance":[],"alleles":["T","C"],"end":140475577,"strand":1,"feature_type":"variation","start":140475577,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140475579,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475579,"source":"dbSNP","seq_region_name":"7","id":"rs940739851","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475580,"feature_type":"variation","strand":1,"end":140475580,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1045730439"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795097328","source":"dbSNP","start":140475582,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140475582,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1241541690","clinical_significance":[],"strand":1,"feature_type":"variation","end":140475586,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475586,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795097431","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140475589,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475589,"source":"dbSNP"},{"seq_region_name":"7","id":"rs562331202","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475591,"source":"dbSNP","strand":1,"feature_type":"variation","end":140475591,"alleles":["G","C"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475593,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140475593,"id":"rs923463515","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140475594,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140475594,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130368222"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1253557761","feature_type":"variation","strand":1,"end":140475595,"alleles":["T","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475595},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140475607,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475607,"clinical_significance":[],"seq_region_name":"7","id":"rs1795097767"},{"clinical_significance":[],"id":"rs376689265","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475610,"feature_type":"variation","strand":1,"end":140475610,"alleles":["G","A"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475617,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140475617,"seq_region_name":"7","id":"rs2130368267","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475618,"feature_type":"variation","strand":1,"end":140475618,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795097905"},{"source":"dbSNP","start":140475622,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140475622,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs769596467"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1477368953","feature_type":"variation","strand":1,"end":140475627,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475627},{"clinical_significance":[],"id":"rs142761884","seq_region_name":"7","alleles":["C","T"],"end":140475637,"feature_type":"variation","strand":1,"source":"dbSNP","start":140475637,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1246079609","source":"dbSNP","start":140475639,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140475639,"alleles":["A","C"],"feature_type":"variation","strand":1},{"end":140475640,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140475640,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795098244"},{"start":140475643,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140475643,"strand":1,"feature_type":"variation","id":"rs1384469462","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795098351","feature_type":"variation","strand":1,"end":140475646,"alleles":["ACA","ACACA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475644},{"clinical_significance":[],"id":"rs1795098401","seq_region_name":"7","source":"dbSNP","start":140475645,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140475645,"alleles":["C","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs181839343","source":"dbSNP","start":140475647,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140475647,"alleles":["G","C"],"feature_type":"variation","strand":1},{"end":140475650,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140475650,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs897481390","clinical_significance":[]},{"seq_region_name":"7","id":"rs1396995428","clinical_significance":[],"alleles":["G","A"],"end":140475651,"strand":1,"feature_type":"variation","start":140475651,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475653,"feature_type":"variation","strand":1,"end":140475653,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795098649"},{"seq_region_name":"7","id":"rs1795098717","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140475655,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475655,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1299788960","end":140475656,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140475656,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795098837","source":"dbSNP","start":140475665,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140475665,"alleles":["A","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795098900","source":"dbSNP","start":140475666,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140475666,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1460456939","seq_region_name":"7","alleles":["AAATACAAATAAATACAAATAAA","AAATACAAATAAA"],"end":140475689,"feature_type":"variation","strand":1,"source":"dbSNP","start":140475667,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140475670,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475670,"clinical_significance":[],"seq_region_name":"7","id":"rs1372575441"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475672,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140475672,"id":"rs10278060","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","C"],"end":140475676,"strand":1,"feature_type":"variation","start":140475676,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1030080036","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795099237","seq_region_name":"7","end":140475680,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140475680,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475682,"source":"dbSNP","strand":1,"feature_type":"variation","end":140475682,"alleles":["C","G"],"seq_region_name":"7","id":"rs1795099283","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1446536979","feature_type":"variation","strand":1,"end":140475686,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475686},{"start":140475693,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140475693,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795099381","clinical_significance":[]},{"start":140475695,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140475695,"alleles":["A","G"],"strand":1,"feature_type":"variation","id":"rs1795099423","seq_region_name":"7","clinical_significance":[]},{"id":"rs1006561159","seq_region_name":"7","clinical_significance":[],"alleles":["AAAA","AA"],"end":140475700,"strand":1,"feature_type":"variation","start":140475697,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140475698,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140475698,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs755194237"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130368554","alleles":["A","C"],"end":140475699,"feature_type":"variation","strand":1,"source":"dbSNP","start":140475699,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1440671769","feature_type":"variation","strand":1,"alleles":["AGAG","AG"],"end":140475703,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475700},{"clinical_significance":[],"id":"rs186931846","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475701,"feature_type":"variation","strand":1,"end":140475701,"alleles":["G","T"]},{"feature_type":"variation","strand":1,"end":140475702,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475702,"clinical_significance":[],"seq_region_name":"7","id":"rs1401846288"},{"seq_region_name":"7","id":"rs192214932","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475707,"source":"dbSNP","strand":1,"feature_type":"variation","end":140475707,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs531586684","source":"dbSNP","start":140475709,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C","G"],"end":140475709,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140475710,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475710,"clinical_significance":[],"seq_region_name":"7","id":"rs1266556068"},{"end":140475727,"alleles":["AAAAATTAAAAATTAAA","AAAAATTAAA"],"strand":1,"feature_type":"variation","start":140475711,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795100061","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795100122","clinical_significance":[],"end":140475717,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140475717,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1020033859","clinical_significance":[],"start":140475723,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140475723,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"end":140475726,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140475726,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795100238","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1338997337","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475727,"feature_type":"variation","strand":1,"alleles":["ACAC","AC"],"end":140475730},{"feature_type":"variation","strand":1,"end":140475758,"alleles":["ACTTGTTTTTTTGTGTATTATTTCAACTAC","AC"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475729,"clinical_significance":[],"seq_region_name":"7","id":"rs1399712454"},{"feature_type":"variation","strand":1,"end":140475730,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475730,"clinical_significance":[],"id":"rs1795100462","seq_region_name":"7"},{"source":"dbSNP","start":140475733,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140475733,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795100526"},{"clinical_significance":[],"id":"rs1795100583","seq_region_name":"7","alleles":["G","-"],"end":140475733,"feature_type":"variation","strand":1,"source":"dbSNP","start":140475733,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs971255577","clinical_significance":[],"end":140475740,"alleles":["TTTTTTT","TTTTTT","TTTTTTTT"],"strand":1,"feature_type":"variation","start":140475734,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs968584859","clinical_significance":[],"alleles":["G","A"],"end":140475741,"strand":1,"feature_type":"variation","start":140475741,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475747,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140475747,"id":"rs1336112447","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","T"],"end":140475752,"strand":1,"feature_type":"variation","start":140475752,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs979417438","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1002706838","feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140475755,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475755},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140475757,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475757,"source":"dbSNP","id":"rs1795100989","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1032334639","seq_region_name":"7","source":"dbSNP","start":140475758,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140475758,"feature_type":"variation","strand":1},{"id":"rs956701141","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475760,"source":"dbSNP","strand":1,"feature_type":"variation","end":140475760,"alleles":["A","C","G"]},{"strand":1,"feature_type":"variation","end":140475766,"alleles":["ACAC","AC"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475763,"source":"dbSNP","id":"rs772318416","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795101222","seq_region_name":"7","source":"dbSNP","start":140475765,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140475765,"alleles":["A","G"],"feature_type":"variation","strand":1},{"end":140475766,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140475766,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130368848","clinical_significance":[]},{"clinical_significance":[],"id":"rs1303712756","seq_region_name":"7","end":140475767,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140475767,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs74330703","clinical_significance":[],"start":140475770,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140475770,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140475773,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475773,"source":"dbSNP","seq_region_name":"7","id":"rs2130368893","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140475777,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475777,"source":"dbSNP","seq_region_name":"7","id":"rs917972364","clinical_significance":[]},{"seq_region_name":"7","id":"rs561518268","clinical_significance":[],"start":140475780,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140475780,"strand":1,"feature_type":"variation"},{"start":140475780,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","-"],"end":140475780,"strand":1,"feature_type":"variation","id":"rs1795101516","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795101584","seq_region_name":"7","feature_type":"variation","strand":1,"end":140475782,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475782},{"feature_type":"variation","strand":1,"end":140475788,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475788,"clinical_significance":[],"id":"rs1585500176","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795101708","clinical_significance":[],"alleles":["G","A"],"end":140475798,"strand":1,"feature_type":"variation","start":140475798,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475800,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140475800,"id":"rs1254949817","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs980939249","clinical_significance":[],"start":140475802,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140475802,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs926875046","source":"dbSNP","start":140475803,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140475803,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140475808,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475808,"clinical_significance":[],"seq_region_name":"7","id":"rs1163151451"},{"seq_region_name":"7","id":"rs1795102009","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475809,"source":"dbSNP","strand":1,"feature_type":"variation","end":140475809,"alleles":["A","G","T"]},{"alleles":["T","C"],"end":140475810,"strand":1,"feature_type":"variation","start":140475810,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130369015","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140475814,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475814,"source":"dbSNP","id":"rs1470672058","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475826,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140475826,"seq_region_name":"7","id":"rs1795102134","clinical_significance":[]},{"id":"rs1795102191","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475827,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140475827},{"strand":1,"feature_type":"variation","end":140475829,"alleles":["T","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475829,"source":"dbSNP","seq_region_name":"7","id":"rs1365761362","clinical_significance":[]},{"start":140475831,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140475831,"alleles":["A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs984819734","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140475835,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475835,"clinical_significance":[],"seq_region_name":"7","id":"rs1795102390"},{"start":140475836,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140475836,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795102438","clinical_significance":[]},{"start":140475846,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140475846,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130369097","clinical_significance":[]},{"seq_region_name":"7","id":"rs942288149","clinical_significance":[],"start":140475857,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140475857,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795102568","alleles":["ACTCAAGGTAACTCAAGGTA","ACTCAAGGTA"],"end":140475876,"feature_type":"variation","strand":1,"source":"dbSNP","start":140475857,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140475866,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140475866,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1268618634","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795102679","clinical_significance":[],"alleles":["C","T"],"end":140475868,"strand":1,"feature_type":"variation","start":140475868,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140475869,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140475869,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1218785399","seq_region_name":"7","clinical_significance":[]},{"start":140475869,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","-"],"end":140475869,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1350744911","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs962051049","end":140475872,"alleles":["AA","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140475871,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1289028150","source":"dbSNP","start":140475873,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140475873,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140475874,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475874,"source":"dbSNP","seq_region_name":"7","id":"rs1795103003","clinical_significance":[]},{"start":140475875,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140475875,"strand":1,"feature_type":"variation","id":"rs1283710520","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140475887,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A","C"],"end":140475887,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs972149467","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1037939206","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475893,"feature_type":"variation","strand":1,"end":140475893,"alleles":["T","C"]},{"start":140475895,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TCT","T"],"end":140475897,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1262137905","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140475899,"alleles":["T","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475899,"source":"dbSNP","seq_region_name":"7","id":"rs1795103333","clinical_significance":[]},{"source":"dbSNP","start":140475902,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140475902,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1236554823"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130369298","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475906,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140475906},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140475907,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475907,"clinical_significance":[],"seq_region_name":"7","id":"rs368633258"},{"end":140475909,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140475909,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795103538","clinical_significance":[]},{"alleles":["G","A","C"],"end":140475911,"strand":1,"feature_type":"variation","start":140475911,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1563098158","clinical_significance":[]},{"start":140475916,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140475922,"alleles":["AATAAAA","AA"],"strand":1,"feature_type":"variation","id":"rs1795103668","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475925,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140475925,"clinical_significance":[],"seq_region_name":"7","id":"rs529082387"},{"seq_region_name":"7","id":"rs1795103835","clinical_significance":[],"start":140475927,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140475927,"alleles":["T","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs933530089","clinical_significance":[],"end":140475935,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140475935,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1343706108","source":"dbSNP","start":140475936,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140475936,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1050515537","feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140475937,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475937},{"seq_region_name":"7","id":"rs1435172113","clinical_significance":[],"end":140475942,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140475942,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795104140","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475944,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140475944},{"source":"dbSNP","start":140475945,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140475945,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs910818129"},{"feature_type":"variation","strand":1,"end":140475952,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475952,"clinical_significance":[],"seq_region_name":"7","id":"rs1795104194"},{"seq_region_name":"7","id":"rs139579114","clinical_significance":[],"end":140475959,"alleles":["ACACA","ACA"],"strand":1,"feature_type":"variation","start":140475955,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140475956,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475956,"source":"dbSNP","seq_region_name":"7","id":"rs1795104314","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140475959,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475959,"source":"dbSNP","seq_region_name":"7","id":"rs1470551997","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795104429","alleles":["A","G"],"end":140475971,"feature_type":"variation","strand":1,"source":"dbSNP","start":140475971,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140475973,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140475973,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1453459708"},{"seq_region_name":"7","id":"rs1795104544","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475974,"source":"dbSNP","strand":1,"feature_type":"variation","end":140475974,"alleles":["G","A"]},{"start":140475975,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140475975,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795104610","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795104675","clinical_significance":[],"end":140475977,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140475977,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475977,"source":"dbSNP","strand":1,"feature_type":"variation","end":140475977,"alleles":["T","TT"],"seq_region_name":"7","id":"rs1795104727","clinical_significance":[]},{"source":"dbSNP","start":140475981,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140475981,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795104787"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475981,"source":"dbSNP","strand":1,"feature_type":"variation","end":140475985,"alleles":["ACACA","ACA"],"seq_region_name":"7","id":"rs1430489942","clinical_significance":[]},{"id":"rs1054023433","seq_region_name":"7","clinical_significance":[],"end":140475984,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140475984,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475993,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140475993,"seq_region_name":"7","id":"rs1479779985","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140475994,"feature_type":"variation","strand":1,"end":140475994,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1197996662"},{"id":"rs1447101818","seq_region_name":"7","clinical_significance":[],"alleles":["C","G"],"end":140475996,"strand":1,"feature_type":"variation","start":140475996,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795105126","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140475999,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140475999},{"id":"rs1585500365","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140476001,"strand":1,"feature_type":"variation","start":140476001,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476002,"feature_type":"variation","strand":1,"end":140476002,"alleles":["A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795105251"},{"end":140476011,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140476011,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1160980994"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795105363","feature_type":"variation","strand":1,"end":140476016,"alleles":["AAAAAA","AAAAAAA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476011},{"seq_region_name":"7","id":"rs1263355963","clinical_significance":[],"start":140476017,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140476017,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1795105476","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476020,"source":"dbSNP","strand":1,"feature_type":"variation","end":140476032,"alleles":["AACCAGTAGGAAA","AA"]},{"strand":1,"feature_type":"variation","alleles":["AACCAGTAGGAAAATACAGGTGA","-"],"end":140476042,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476020,"source":"dbSNP","seq_region_name":"7","id":"rs1203055617","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476026,"source":"dbSNP","strand":1,"feature_type":"variation","end":140476026,"alleles":["T","C","G"],"seq_region_name":"7","id":"rs892823416","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1263594792","end":140476027,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140476027,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1795105724","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476031,"feature_type":"variation","strand":1,"end":140476031,"alleles":["A","C"]},{"clinical_significance":[],"id":"rs1795105823","seq_region_name":"7","source":"dbSNP","start":140476032,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140476032,"alleles":["A","G"],"feature_type":"variation","strand":1},{"end":140476034,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140476034,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs183498887","clinical_significance":[]},{"id":"rs370283297","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476036,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140476036},{"strand":1,"feature_type":"variation","end":140476037,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476037,"source":"dbSNP","seq_region_name":"7","id":"rs1321259289","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140476039,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476039,"source":"dbSNP","seq_region_name":"7","id":"rs1795106239","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140476040,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476040,"clinical_significance":[],"seq_region_name":"7","id":"rs1282583024"},{"strand":1,"feature_type":"variation","end":140476041,"alleles":["G","GG"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476041,"source":"dbSNP","seq_region_name":"7","id":"rs1431516897","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140476045,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476045,"clinical_significance":[],"seq_region_name":"7","id":"rs73735281"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140476046,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476046,"source":"dbSNP","id":"rs117298880","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476047,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C","T"],"end":140476047,"id":"rs187977189","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs747173350","feature_type":"variation","strand":1,"alleles":["A","-"],"end":140476048,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476048},{"feature_type":"variation","strand":1,"end":140476050,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476050,"clinical_significance":[],"id":"rs1795107001","seq_region_name":"7"},{"id":"rs774909572","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140476051,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476051,"source":"dbSNP"},{"end":140476055,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140476055,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1300157203","clinical_significance":[]},{"id":"rs1795107287","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476055,"source":"dbSNP","strand":1,"feature_type":"variation","end":140476059,"alleles":["AAAAA","AAA"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1335835020","feature_type":"variation","strand":1,"end":140476060,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476060},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795107476","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476061,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140476061},{"alleles":["A","C"],"end":140476066,"strand":1,"feature_type":"variation","start":140476066,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795107540","clinical_significance":[]},{"seq_region_name":"7","id":"rs904354482","clinical_significance":[],"start":140476067,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140476067,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140476070,"alleles":["A","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476070,"clinical_significance":[],"seq_region_name":"7","id":"rs1374347921"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476070,"feature_type":"variation","strand":1,"end":140476073,"alleles":["AAAA","AAA"],"clinical_significance":[],"id":"rs1795107744","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs760029780","source":"dbSNP","start":140476074,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140476074,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795107937","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476077,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140476077},{"source":"dbSNP","start":140476078,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140476078,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1352841453"},{"seq_region_name":"7","id":"rs1795108085","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140476080,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476080,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140476081,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476081,"clinical_significance":[],"seq_region_name":"7","id":"rs1243388130"},{"alleles":["T","A"],"end":140476082,"strand":1,"feature_type":"variation","start":140476082,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795108193","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795108249","source":"dbSNP","start":140476083,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140476083,"alleles":["G","A"],"feature_type":"variation","strand":1},{"alleles":["GAAGAA","GAA"],"end":140476088,"feature_type":"variation","strand":1,"source":"dbSNP","start":140476083,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1205274828"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795108367","end":140476086,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140476086,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795108425","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476089,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140476089},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140476091,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476091,"source":"dbSNP","seq_region_name":"7","id":"rs1459834937","clinical_significance":[]},{"seq_region_name":"7","id":"rs1034153286","clinical_significance":[],"strand":1,"feature_type":"variation","end":140476097,"alleles":["T","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476097,"source":"dbSNP"},{"id":"rs1341544037","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140476099,"strand":1,"feature_type":"variation","start":140476099,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476101,"source":"dbSNP","strand":1,"feature_type":"variation","end":140476101,"alleles":["C","G"],"id":"rs1268559395","seq_region_name":"7","clinical_significance":[]},{"end":140476109,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140476109,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795108705","seq_region_name":"7"},{"seq_region_name":"7","id":"rs958670930","clinical_significance":[],"strand":1,"feature_type":"variation","end":140476113,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476113,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476115,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140476115,"clinical_significance":[],"seq_region_name":"7","id":"rs1383731447"},{"seq_region_name":"7","id":"rs1006576816","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140476116,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476116,"source":"dbSNP"},{"clinical_significance":[],"id":"rs569957528","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476118,"feature_type":"variation","strand":1,"end":140476118,"alleles":["G","A","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795109047","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476121,"feature_type":"variation","strand":1,"end":140476121,"alleles":["T","C"]},{"strand":1,"feature_type":"variation","end":140476122,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476122,"source":"dbSNP","seq_region_name":"7","id":"rs534609185","clinical_significance":[]},{"alleles":["T","C"],"end":140476124,"strand":1,"feature_type":"variation","start":140476124,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1412190798","clinical_significance":[]},{"id":"rs1398006571","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140476125,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476125,"source":"dbSNP"},{"alleles":["T","C"],"end":140476126,"strand":1,"feature_type":"variation","start":140476126,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs151042927","seq_region_name":"7","clinical_significance":[]},{"id":"rs1025498423","seq_region_name":"7","clinical_significance":[],"end":140476129,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140476129,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140476129,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140476132,"alleles":["TATA","TATATA"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1266861984","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476130,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140476130,"id":"rs954759071","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476131,"feature_type":"variation","strand":1,"end":140476131,"alleles":["T","A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs970808878"},{"alleles":["A","T"],"end":140476132,"strand":1,"feature_type":"variation","start":140476132,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795109996","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476133,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GGG","GG"],"end":140476135,"seq_region_name":"7","id":"rs1236742228","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795110044","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140476134,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476134,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1458282605","source":"dbSNP","start":140476135,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140476135,"alleles":["G","C"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476141,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140476141,"seq_region_name":"7","id":"rs1795110163","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476144,"source":"dbSNP","strand":1,"feature_type":"variation","end":140476144,"alleles":["G","A"],"id":"rs1180537837","seq_region_name":"7","clinical_significance":[]},{"start":140476152,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140476152,"alleles":["A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795110274","clinical_significance":[]},{"alleles":["C","A"],"end":140476153,"feature_type":"variation","strand":1,"source":"dbSNP","start":140476153,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1439420895"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1270815752","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476159,"feature_type":"variation","strand":1,"end":140476159,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs986280911","clinical_significance":[],"start":140476162,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140476162,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140476163,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140476163,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs910733937"},{"end":140476164,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140476164,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795110661","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140476165,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476165,"source":"dbSNP","id":"rs1795110722","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs981249636","seq_region_name":"7","end":140476167,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140476167,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795110847","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476168,"source":"dbSNP","strand":1,"feature_type":"variation","end":140476168,"alleles":["A","AA"]},{"clinical_significance":[],"id":"rs1244122787","seq_region_name":"7","source":"dbSNP","start":140476170,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140476170,"alleles":["C","T"],"feature_type":"variation","strand":1},{"id":"rs1764160024","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140476172,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476172,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140476173,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476173,"clinical_significance":[],"seq_region_name":"7","id":"rs1795110946"},{"end":140476179,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140476179,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1382486022","seq_region_name":"7"},{"source":"dbSNP","start":140476181,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140476181,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1280576446"},{"source":"dbSNP","start":140476183,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140476183,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs189711517"},{"clinical_significance":[],"id":"rs926801386","seq_region_name":"7","alleles":["T","C"],"end":140476186,"feature_type":"variation","strand":1,"source":"dbSNP","start":140476186,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476187,"source":"dbSNP","strand":1,"feature_type":"variation","end":140476187,"alleles":["G","A"],"seq_region_name":"7","id":"rs1353214383","clinical_significance":[]},{"clinical_significance":[],"id":"rs369627492","seq_region_name":"7","source":"dbSNP","start":140476192,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140476192,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1379038336","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476194,"source":"dbSNP","strand":1,"feature_type":"variation","end":140476194,"alleles":["T","C","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795111552","source":"dbSNP","start":140476197,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140476197,"alleles":["C","G","T"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140476200,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476200,"source":"dbSNP","seq_region_name":"7","id":"rs1439668885","clinical_significance":[]},{"start":140476201,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140476201,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795111661","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476202,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140476202,"id":"rs371916087","seq_region_name":"7","clinical_significance":[]},{"alleles":["ATAT","AT"],"end":140476205,"strand":1,"feature_type":"variation","start":140476202,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1164753077","clinical_significance":[]},{"start":140476203,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140476203,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795111940","clinical_significance":[]},{"start":140476205,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140476205,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1165070666","clinical_significance":[]},{"clinical_significance":[],"id":"rs1456649392","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476207,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140476207},{"clinical_significance":[],"seq_region_name":"7","id":"rs942173858","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476212,"feature_type":"variation","strand":1,"end":140476212,"alleles":["T","A","C"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476212,"feature_type":"variation","strand":1,"alleles":["TGTTT","T"],"end":140476216,"clinical_significance":[],"seq_region_name":"7","id":"rs1795112339"},{"clinical_significance":[],"seq_region_name":"7","id":"rs990172285","end":140476213,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140476213,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140476216,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140476216,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1471053140","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795112623","seq_region_name":"7","alleles":["A","G"],"end":140476217,"feature_type":"variation","strand":1,"source":"dbSNP","start":140476217,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795112728","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140476219,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476219,"source":"dbSNP"},{"seq_region_name":"7","id":"rs535266588","clinical_significance":[],"start":140476220,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140476220,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1231066437","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476221,"feature_type":"variation","strand":1,"end":140476221,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795113005","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476227,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140476227},{"seq_region_name":"7","id":"rs569669438","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476229,"source":"dbSNP","strand":1,"feature_type":"variation","end":140476229,"alleles":["G","A","T"]},{"clinical_significance":[],"id":"rs2130370602","seq_region_name":"7","end":140476230,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140476230,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","G"],"end":140476232,"feature_type":"variation","strand":1,"source":"dbSNP","start":140476232,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795113187"},{"clinical_significance":[],"id":"rs1490528093","seq_region_name":"7","source":"dbSNP","start":140476234,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140476234,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476236,"feature_type":"variation","strand":1,"end":140476236,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs553575845"},{"source":"dbSNP","start":140476238,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140476238,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795113452"},{"seq_region_name":"7","id":"rs572151998","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476240,"source":"dbSNP","strand":1,"feature_type":"variation","end":140476240,"alleles":["T","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1321280864","end":140476242,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140476242,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1285242420","clinical_significance":[],"strand":1,"feature_type":"variation","end":140476250,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476250,"source":"dbSNP"},{"source":"dbSNP","start":140476263,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140476263,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795113804","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476265,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140476265,"seq_region_name":"7","id":"rs867052976","clinical_significance":[]},{"source":"dbSNP","start":140476266,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140476266,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs928968188"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795114032","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476271,"feature_type":"variation","strand":1,"end":140476273,"alleles":["CCC","CC"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1375490242","end":140476278,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140476278,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795114158","clinical_significance":[],"alleles":["T","A"],"end":140476279,"strand":1,"feature_type":"variation","start":140476279,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1371676683","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140476282,"strand":1,"feature_type":"variation","start":140476282,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140476283,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140476283,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1051415847"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563098334","feature_type":"variation","strand":1,"end":140476287,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476287},{"seq_region_name":"7","id":"rs1248947838","clinical_significance":[],"start":140476288,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140476340,"alleles":["ATGTTTACTTACTGAATGATTGAATAAGGTAGTTCCAGAAAAAATATACATGT","ATGT"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs890218261","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476291,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140476291},{"alleles":["T","C"],"end":140476292,"feature_type":"variation","strand":1,"source":"dbSNP","start":140476292,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs139725038","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795114503","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476296,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TTACTGAATGATT","TT"],"end":140476308},{"alleles":["T","C"],"end":140476297,"feature_type":"variation","strand":1,"source":"dbSNP","start":140476297,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs73491007","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795114636","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140476299,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476299,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476305,"feature_type":"variation","strand":1,"end":140476305,"alleles":["G","A"],"clinical_significance":[],"id":"rs1243725338","seq_region_name":"7"},{"seq_region_name":"7","id":"rs904397319","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140476307,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476307,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140476311,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476311,"clinical_significance":[],"seq_region_name":"7","id":"rs1795114815"},{"seq_region_name":"7","id":"rs1795114869","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476317,"source":"dbSNP","strand":1,"feature_type":"variation","end":140476317,"alleles":["T","G"]},{"seq_region_name":"7","id":"rs1795114918","clinical_significance":[],"strand":1,"feature_type":"variation","end":140476320,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476320,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795114985","clinical_significance":[],"alleles":["G","C"],"end":140476325,"strand":1,"feature_type":"variation","start":140476325,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140476331,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476331,"clinical_significance":[],"seq_region_name":"7","id":"rs1348890656"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476332,"feature_type":"variation","strand":1,"end":140476332,"alleles":["T","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs999949893"},{"source":"dbSNP","start":140476334,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140476334,"alleles":["T","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795115135","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1159422182","alleles":["A","C","G"],"end":140476337,"feature_type":"variation","strand":1,"source":"dbSNP","start":140476337,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140476338,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140476338,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795115243"},{"seq_region_name":"7","id":"rs1318826445","clinical_significance":[],"alleles":["G","A"],"end":140476339,"strand":1,"feature_type":"variation","start":140476339,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1402202658","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140476344,"alleles":["CC","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476343,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476344,"source":"dbSNP","strand":1,"feature_type":"variation","end":140476344,"alleles":["C","T"],"seq_region_name":"7","id":"rs552898314","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs530665762","feature_type":"variation","strand":1,"end":140476345,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476345},{"source":"dbSNP","start":140476348,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140476348,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1236489243"},{"clinical_significance":[],"id":"rs1795115628","seq_region_name":"7","end":140476349,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140476349,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1457365347","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476352,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140476352},{"id":"rs1795115751","seq_region_name":"7","clinical_significance":[],"start":140476361,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140476361,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140476363,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476363,"source":"dbSNP","seq_region_name":"7","id":"rs1009995630","clinical_significance":[]},{"source":"dbSNP","start":140476364,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140476364,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1197296250"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795115925","alleles":["A","G","T"],"end":140476365,"feature_type":"variation","strand":1,"source":"dbSNP","start":140476365,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1488213944","seq_region_name":"7","clinical_significance":[],"alleles":["G","A","C"],"end":140476366,"strand":1,"feature_type":"variation","start":140476366,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795116046","clinical_significance":[],"start":140476371,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140476371,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"alleles":["G","A"],"end":140476375,"feature_type":"variation","strand":1,"source":"dbSNP","start":140476375,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795116099"},{"strand":1,"feature_type":"variation","end":140476380,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476380,"source":"dbSNP","seq_region_name":"7","id":"rs1025004182","clinical_significance":[]},{"seq_region_name":"7","id":"rs1218266172","clinical_significance":[],"end":140476383,"alleles":["GAGA","GA"],"strand":1,"feature_type":"variation","start":140476380,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795116270","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476383,"feature_type":"variation","strand":1,"end":140476384,"alleles":["AA","AAA"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs543292870","end":140476386,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140476386,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140476387,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476387,"source":"dbSNP","seq_region_name":"7","id":"rs754056154","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795116501","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["GCTTGAACCCAGGAGGCAGAGGTTGCAGTGAGCTGAGATCTCGCCACTGCACTCCAGC","GCTTGAACCCAGGAGGCAGAGGTTGCAGTGAGCTGAGATCTCGCCACTGCACTCCAGCTTGAACCCAGGAGGCAGAGGTTGCAGTGAGCTGAGATCTCGCCACTGCACTCCAGC"],"end":140476444,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476387},{"seq_region_name":"7","id":"rs1795116558","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476394,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140476394},{"seq_region_name":"7","id":"rs1795116617","clinical_significance":[],"alleles":["A","G"],"end":140476397,"strand":1,"feature_type":"variation","start":140476397,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140476398,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140476398,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1326202310","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140476407,"alleles":["AGAG","AGAGAG"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476404,"clinical_significance":[],"seq_region_name":"7","id":"rs566649454"},{"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140476407,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476407,"clinical_significance":[],"seq_region_name":"7","id":"rs1795116815"},{"clinical_significance":[],"seq_region_name":"7","id":"rs761935687","source":"dbSNP","start":140476408,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140476408,"alleles":["G","C"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476409,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140476409,"clinical_significance":[],"seq_region_name":"7","id":"rs1585500967"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585500972","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476416,"feature_type":"variation","strand":1,"end":140476416,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795117070","alleles":["T","G"],"end":140476420,"feature_type":"variation","strand":1,"source":"dbSNP","start":140476420,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140476423,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140476423,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795117121","clinical_significance":[]},{"seq_region_name":"7","id":"rs376738656","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476428,"source":"dbSNP","strand":1,"feature_type":"variation","end":140476428,"alleles":["C","T"]},{"source":"dbSNP","start":140476429,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140476429,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1466906453"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795117297","source":"dbSNP","start":140476430,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140476430,"alleles":["C","T"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140476434,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476434,"source":"dbSNP","seq_region_name":"7","id":"rs1795117366","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1399002390","alleles":["G","A"],"end":140476435,"feature_type":"variation","strand":1,"source":"dbSNP","start":140476435,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795117478","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["GCACTCCAGCCTGGGCGACAGAGCG","GCACTCCAGCCTGGGCGACAGAGCGGCACTCCAGCCTGGGCGACAGAGCG"],"end":140476459,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476435,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs149800514","feature_type":"variation","strand":1,"end":140476436,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476436},{"seq_region_name":"7","id":"rs897708045","clinical_significance":[],"strand":1,"feature_type":"variation","end":140476437,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476437,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476439,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140476439,"seq_region_name":"7","id":"rs1585501005","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs993467380","alleles":["C","G"],"end":140476440,"feature_type":"variation","strand":1,"source":"dbSNP","start":140476440,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140476446,"alleles":["T","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476446,"source":"dbSNP","seq_region_name":"7","id":"rs1795117847","clinical_significance":[]},{"start":140476449,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140476462,"alleles":["GCGACAGAGCGACA","GCGACA"],"strand":1,"feature_type":"variation","id":"rs1795117922","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476450,"source":"dbSNP","strand":1,"feature_type":"variation","end":140476450,"alleles":["C","G","T"],"seq_region_name":"7","id":"rs146843628","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140476451,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476451,"source":"dbSNP","id":"rs1470138080","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1376827594","clinical_significance":[],"strand":1,"feature_type":"variation","end":140476452,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476452,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1395275551","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140476453,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476453},{"seq_region_name":"7","id":"rs1431291775","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140476455,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476455,"source":"dbSNP"},{"seq_region_name":"7","id":"rs540876854","clinical_significance":[],"start":140476458,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140476458,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476459,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["-","T"],"end":140476458,"seq_region_name":"7","id":"rs1795118360","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1009380120","alleles":["G","A","C"],"end":140476459,"feature_type":"variation","strand":1,"source":"dbSNP","start":140476459,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1220758641","clinical_significance":[],"alleles":["C","G"],"end":140476461,"strand":1,"feature_type":"variation","start":140476461,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585501065","source":"dbSNP","start":140476462,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140476462,"alleles":["A","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1795118595","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476463,"feature_type":"variation","strand":1,"end":140476463,"alleles":["C","T"]},{"strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140476464,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476464,"source":"dbSNP","id":"rs1256318439","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476465,"source":"dbSNP","strand":1,"feature_type":"variation","end":140476465,"alleles":["C","T"],"id":"rs1795118716","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1317384950","clinical_significance":[],"alleles":["C","A"],"end":140476466,"strand":1,"feature_type":"variation","start":140476466,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["T","A","C","G"],"end":140476468,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476468,"source":"dbSNP","id":"rs1473694056","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140476469,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476469,"source":"dbSNP","seq_region_name":"7","id":"rs1180234548","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140476470,"alleles":["T","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476470,"source":"dbSNP","seq_region_name":"7","id":"rs1413140697","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795119028","clinical_significance":[],"strand":1,"feature_type":"variation","end":140476470,"alleles":["-","A","AA","AAA","AAAA","AAAAA","AAAAAAA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476471,"source":"dbSNP"},{"id":"rs372207882","seq_region_name":"7","clinical_significance":[],"start":140476471,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140476471,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795119234","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476471,"feature_type":"variation","strand":1,"end":140476471,"alleles":["C","-"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795119286","feature_type":"variation","strand":1,"end":140476472,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476472},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476472,"feature_type":"variation","strand":1,"alleles":["AAAAAAAAAAAAAAAAAA","AAAAAAAAA","AAAAAAAAAA","AAAAAAAAAAA","AAAAAAAAAAAAA","AAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA"],"end":140476489,"clinical_significance":[],"seq_region_name":"7","id":"rs59392050"},{"end":140476474,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140476474,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1258319670","seq_region_name":"7"},{"start":140476474,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140476489,"alleles":["AAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAATGGAAAAAAAAAAAAAAAA"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130371768","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130371773","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476475,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAATGGAAGAAAAAAAAAAAAAAA"],"end":140476489},{"seq_region_name":"7","id":"rs1795119958","clinical_significance":[],"strand":1,"feature_type":"variation","end":140476476,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476476,"source":"dbSNP"},{"seq_region_name":"7","id":"rs2130371793","clinical_significance":[],"strand":1,"feature_type":"variation","end":140476489,"alleles":["AAAAAAAAAAAA","AAAAAAAAAAAAAATGGAAAAAAAAAAAA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476478,"source":"dbSNP"},{"start":140476485,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140476485,"alleles":["A","G"],"strand":1,"feature_type":"variation","id":"rs1795120018","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140476486,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140476486,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585501163"},{"seq_region_name":"7","id":"rs1184483900","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476489,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140476489},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476490,"feature_type":"variation","strand":1,"alleles":["-","T"],"end":140476489,"clinical_significance":[],"seq_region_name":"7","id":"rs1795120179"},{"alleles":["G","A"],"end":140476490,"feature_type":"variation","strand":1,"source":"dbSNP","start":140476490,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1181768286"},{"strand":1,"feature_type":"variation","end":140476491,"alleles":["GG","G","GGG"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476490,"source":"dbSNP","seq_region_name":"7","id":"rs1446801781","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1200383047","feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140476491,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476491},{"feature_type":"variation","strand":1,"end":140476494,"alleles":["G","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476494,"clinical_significance":[],"seq_region_name":"7","id":"rs1479005298"},{"seq_region_name":"7","id":"rs1795120547","clinical_significance":[],"start":140476495,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["ATACACAT","ATACACATACACAT"],"end":140476502,"strand":1,"feature_type":"variation"},{"start":140476496,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140476496,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1191071321","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476496,"feature_type":"variation","strand":1,"alleles":["TACAC","TACACTACAC"],"end":140476500,"clinical_significance":[],"id":"rs1795120681","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795120739","feature_type":"variation","strand":1,"end":140476497,"alleles":["A","AA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476497},{"start":140476498,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140476498,"alleles":["C","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1422398495","clinical_significance":[]},{"start":140476499,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140476499,"alleles":["A","C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1253614350","clinical_significance":[]},{"alleles":["C","T"],"end":140476500,"feature_type":"variation","strand":1,"source":"dbSNP","start":140476500,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795120920"},{"source":"dbSNP","start":140476501,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140476502,"alleles":["AT","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1205952640"},{"start":140476502,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140476502,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1339496017","clinical_significance":[]},{"id":"rs2130372014","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476503,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140476503},{"strand":1,"feature_type":"variation","alleles":["G","-"],"end":140476505,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476505,"source":"dbSNP","seq_region_name":"7","id":"rs758877021","clinical_significance":[]},{"source":"dbSNP","start":140476505,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140476505,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795121075"},{"alleles":["C","T"],"end":140476508,"strand":1,"feature_type":"variation","start":140476508,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795121177","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130372060","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476510,"source":"dbSNP","strand":1,"feature_type":"variation","end":140476510,"alleles":["G","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795121226","feature_type":"variation","strand":1,"end":140476511,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476511},{"id":"rs1246331250","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["TT","T"],"end":140476512,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476511,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1177558841","feature_type":"variation","strand":1,"alleles":["GTACTTTGTCTTTGGT","-"],"end":140476530,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476515},{"end":140476515,"alleles":["-","AAAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140476516,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795121395"},{"seq_region_name":"7","id":"rs182332176","clinical_significance":[],"start":140476517,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140476517,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476518,"source":"dbSNP","strand":1,"feature_type":"variation","end":140476518,"alleles":["C","A","G","T"],"seq_region_name":"7","id":"rs1395251730","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795121617","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476518,"feature_type":"variation","strand":1,"end":140476518,"alleles":["C","-"]},{"strand":1,"feature_type":"variation","alleles":["CTTTGT","G"],"end":140476523,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476518,"source":"dbSNP","seq_region_name":"7","id":"rs1554450903","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs535467637","feature_type":"variation","strand":1,"alleles":["CTTTGTCTTTG","CTTTG"],"end":140476528,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476518},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795121792","end":140476520,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140476520,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1795121836","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476521,"source":"dbSNP","strand":1,"feature_type":"variation","end":140476521,"alleles":["T","C"]},{"start":140476522,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140476522,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585501268","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476523,"feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140476523,"clinical_significance":[],"id":"rs1795121931","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1585501279","seq_region_name":"7","source":"dbSNP","start":140476524,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140476524,"alleles":["C","T"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140476535,"alleles":["TTTGGTAATTT","TTTGGTAATTTGGTAATTT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476525,"clinical_significance":[],"seq_region_name":"7","id":"rs2130372231"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1465529948","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140476526,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476526},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140476527,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476527,"clinical_significance":[],"seq_region_name":"7","id":"rs1299847782"},{"seq_region_name":"7","id":"rs1585501299","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140476528,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476528,"source":"dbSNP"},{"alleles":["T","A"],"end":140476534,"strand":1,"feature_type":"variation","start":140476534,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1289366682","clinical_significance":[]},{"end":140476537,"alleles":["C","A","G"],"strand":1,"feature_type":"variation","start":140476537,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1362219985","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795122365","clinical_significance":[],"strand":1,"feature_type":"variation","end":140476538,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476538,"source":"dbSNP"},{"id":"rs1795122413","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140476540,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476540,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1795122479","seq_region_name":"7","alleles":["TTTT","TT","TTTTT"],"end":140476544,"feature_type":"variation","strand":1,"source":"dbSNP","start":140476541,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140476548,"alleles":["TTTGTTT","TTT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140476542,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1164440426"},{"id":"rs1795122619","seq_region_name":"7","clinical_significance":[],"start":140476543,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140476543,"alleles":["T","C","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs954690886","feature_type":"variation","strand":1,"alleles":["TTGTT","TT"],"end":140476547,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476543},{"clinical_significance":[],"seq_region_name":"7","id":"rs1340071684","end":140476546,"alleles":["TGT","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140476544,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs377589590","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476545,"feature_type":"variation","strand":1,"alleles":["G","-"],"end":140476545},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140476545,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476545,"source":"dbSNP","seq_region_name":"7","id":"rs866850446","clinical_significance":[]},{"source":"dbSNP","start":140476546,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140476546,"alleles":["T","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1361079403","seq_region_name":"7"},{"clinical_significance":[],"id":"rs72087358","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["TTTTTTTTTTTTTT","TTTTTTTTTTT","TTTTTTTTTTTT","TTTTTTTTTTTTT","TTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTT"],"end":140476559,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476546},{"strand":1,"feature_type":"variation","end":140476547,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476547,"source":"dbSNP","seq_region_name":"7","id":"rs1303560533","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476548,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","G"],"end":140476548,"seq_region_name":"7","id":"rs1310503292","clinical_significance":[]},{"source":"dbSNP","start":140476549,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140476549,"alleles":["T","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1210115660","seq_region_name":"7"},{"seq_region_name":"7","id":"rs533427309","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476550,"source":"dbSNP","strand":1,"feature_type":"variation","end":140476550,"alleles":["T","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1489483624","source":"dbSNP","start":140476551,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140476551,"alleles":["T","G"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476552,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140476552,"clinical_significance":[],"seq_region_name":"7","id":"rs1214841699"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1017679635","feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140476553,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476553},{"clinical_significance":[],"seq_region_name":"7","id":"rs958486130","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140476554,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476554},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476557,"source":"dbSNP","strand":1,"feature_type":"variation","end":140476557,"alleles":["T","C"],"id":"rs1585501439","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140476559,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476559,"source":"dbSNP","id":"rs989623056","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476559,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TA","-"],"end":140476560,"seq_region_name":"7","id":"rs1388788231","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1478176048","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476560,"feature_type":"variation","strand":1,"end":140476560,"alleles":["A","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795123835","feature_type":"variation","strand":1,"alleles":["AA","A"],"end":140476561,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476560},{"start":140476561,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140476561,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1192552488","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140476562,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476562,"source":"dbSNP","seq_region_name":"7","id":"rs1422522177","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476563,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140476563,"clinical_significance":[],"seq_region_name":"7","id":"rs1432090915"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476563,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GAAAG","GAAAGAAAG"],"end":140476567,"id":"rs1795124052","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795124107","source":"dbSNP","start":140476566,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AGCAG","AG"],"end":140476570,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476568,"feature_type":"variation","strand":1,"end":140476568,"alleles":["C","T"],"clinical_significance":[],"id":"rs1795124165","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs868590595","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476572,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140476572},{"strand":1,"feature_type":"variation","end":140476573,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476573,"source":"dbSNP","seq_region_name":"7","id":"rs1795124286","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1362324817","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476575,"feature_type":"variation","strand":1,"end":140476575,"alleles":["A","T"]},{"start":140476578,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140476578,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1157577733","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130372651","source":"dbSNP","start":140476581,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140476581,"feature_type":"variation","strand":1},{"end":140476583,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140476583,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585501496"},{"clinical_significance":[],"id":"rs1795124460","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140476586,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476586},{"seq_region_name":"7","id":"rs1417664472","clinical_significance":[],"end":140476599,"alleles":["TGTTAAAGTG","TG"],"strand":1,"feature_type":"variation","start":140476590,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1297397660","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140476591,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476591,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1270250316","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476594,"feature_type":"variation","strand":1,"end":140476594,"alleles":["A","G","T"]},{"seq_region_name":"7","id":"rs1033756865","clinical_significance":[],"start":140476599,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140476599,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"end":140476607,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140476607,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs914145692","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795124831","clinical_significance":[],"start":140476608,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140476608,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130372766","feature_type":"variation","strand":1,"end":140476609,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476609},{"source":"dbSNP","start":140476610,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140476610,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1365937733"},{"start":140476611,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140476611,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795124945","clinical_significance":[]},{"seq_region_name":"7","id":"rs1208921027","clinical_significance":[],"alleles":["A","G"],"end":140476613,"strand":1,"feature_type":"variation","start":140476613,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1437527781","end":140476616,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140476616,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs945579788","end":140476617,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140476617,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795125161","clinical_significance":[],"alleles":["TTT","T"],"end":140476622,"strand":1,"feature_type":"variation","start":140476620,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476622,"feature_type":"variation","strand":1,"end":140476622,"alleles":["T","C"],"clinical_significance":[],"id":"rs1795125220","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795125264","clinical_significance":[],"alleles":["A","G"],"end":140476623,"strand":1,"feature_type":"variation","start":140476623,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140476627,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476627,"source":"dbSNP","seq_region_name":"7","id":"rs1795125314","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476630,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","G"],"end":140476630,"id":"rs1262343108","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476633,"source":"dbSNP","strand":1,"feature_type":"variation","end":140476633,"alleles":["C","G"],"seq_region_name":"7","id":"rs1795125403","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476634,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140476634,"clinical_significance":[],"seq_region_name":"7","id":"rs1795125450"},{"feature_type":"variation","strand":1,"end":140476638,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476638,"clinical_significance":[],"seq_region_name":"7","id":"rs1795125509"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476641,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140476641,"clinical_significance":[],"seq_region_name":"7","id":"rs1295499743"},{"seq_region_name":"7","id":"rs963548171","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140476642,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476642,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476645,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CTCAGTATCTGCTCAG","CTCAG"],"end":140476660,"seq_region_name":"7","id":"rs1585501541","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs551597767","end":140476647,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140476647,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1365587459","alleles":["CA","CACA"],"end":140476648,"feature_type":"variation","strand":1,"source":"dbSNP","start":140476647,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476649,"feature_type":"variation","strand":1,"end":140476649,"alleles":["G","C"],"clinical_significance":[],"id":"rs1328322457","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1283878792","feature_type":"variation","strand":1,"end":140476650,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476650},{"seq_region_name":"7","id":"rs1795125893","clinical_significance":[],"alleles":["A","G"],"end":140476651,"strand":1,"feature_type":"variation","start":140476651,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140476652,"alleles":["T","A","G"],"strand":1,"feature_type":"variation","start":140476652,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs563669187","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1329462762","source":"dbSNP","start":140476653,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140476653,"feature_type":"variation","strand":1},{"end":140476656,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140476656,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs530954609","clinical_significance":[]},{"seq_region_name":"7","id":"rs575355799","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476657,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TCAGG","TCAGGTCAGG","TCAGGTCAGTCAGG"],"end":140476661},{"alleles":["C","G"],"end":140476658,"feature_type":"variation","strand":1,"source":"dbSNP","start":140476658,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795126208","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795126266","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476658,"feature_type":"variation","strand":1,"alleles":["CAGGATACTCAGTAACTGAGTATCCTGTTCATGATACTGGAAC","CAGGATACTCAGTAACTGAGTATCCTGTTCATGATACTGGAACAGGATACTCAGTAACTGAGTATCCTGTTCATGATACTGGAAC"],"end":140476700},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476660,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140476660,"clinical_significance":[],"id":"rs549680663","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1022287698","source":"dbSNP","start":140476661,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["GATACTCAGTAACTGAGTATCCTGTTCATGATACT","GATACT","GATACTCAGTAACTGAGTATCCTGTTCATGATACTCAGTAACTGAGTATCCTGTTAATGATACTCAGTAACTGAGTATCCTGTTCATGATACT","GATACTCAGTAACTGAGTATCCTGTTCATGATACTCAGTAACTGAGTATCCTGTTCATGATACT","GATACTCAGTAACTGAGTATCCTGTTCATGATACTCAGTAACTGAGTATCCTGTTCATGATACTCAGTAACTGAGTATCCTGTTCATGATACTCAGTAACTGAGTATCCTGTTCATGATACT"],"end":140476695,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1457065094","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476662,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140476662},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476662,"feature_type":"variation","strand":1,"alleles":["ATACTCAGTAA","A"],"end":140476672,"clinical_significance":[],"seq_region_name":"7","id":"rs1356420717"},{"clinical_significance":[],"id":"rs1795126638","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476664,"feature_type":"variation","strand":1,"alleles":["ACTCAGTAACT","ACT"],"end":140476674},{"strand":1,"feature_type":"variation","end":140476665,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476665,"source":"dbSNP","seq_region_name":"7","id":"rs1795126692","clinical_significance":[]},{"seq_region_name":"7","id":"rs1430558720","clinical_significance":[],"strand":1,"feature_type":"variation","end":140476669,"alleles":["AG","AGAG"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476668,"source":"dbSNP"},{"source":"dbSNP","start":140476668,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140476679,"alleles":["AGTAACTGAGTA","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1179258532"},{"feature_type":"variation","strand":1,"alleles":["AGTAACTGAGTATCCTGTTCATGATACTG","AGTAACTGAGTATCCTGTTCATGATACTGAGTAACTGAGTATCCTGTTCATGATACTG"],"end":140476696,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476668,"clinical_significance":[],"seq_region_name":"7","id":"rs1795126855"},{"seq_region_name":"7","id":"rs1795126904","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476669,"source":"dbSNP","strand":1,"feature_type":"variation","end":140476669,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585501626","feature_type":"variation","strand":1,"end":140476669,"alleles":["-","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476670},{"clinical_significance":[],"seq_region_name":"7","id":"rs1478711838","source":"dbSNP","start":140476670,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140476670,"alleles":["T","A"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140476671,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476671,"source":"dbSNP","seq_region_name":"7","id":"rs1375485450","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795127117","feature_type":"variation","strand":1,"alleles":["AACTGAGTATCCTGTTCATGATACTGGAACTGAG","AACTGAG"],"end":140476704,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476671},{"feature_type":"variation","strand":1,"alleles":["-","CTGAGAT"],"end":140476671,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476672,"clinical_significance":[],"id":"rs1585501640","seq_region_name":"7"},{"id":"rs1795127241","seq_region_name":"7","clinical_significance":[],"start":140476673,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["CTGAGTATCCTGTTCATGATACT","CTGAGTATCCTGTTCATGATACTCAGTAACTGAGTATCCTGTTCATGATACTCAGTACCTGAGTATCCTGTTCATGATACT"],"end":140476695,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1795127303","clinical_significance":[],"start":140476675,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140476675,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"alleles":["-","TATACTC"],"end":140476675,"feature_type":"variation","strand":1,"source":"dbSNP","start":140476676,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585501648"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1197720483","feature_type":"variation","strand":1,"alleles":["AG","AGATACTGTATACTCAG"],"end":140476677,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476676},{"clinical_significance":[],"id":"rs1795127464","seq_region_name":"7","source":"dbSNP","start":140476681,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140476681,"alleles":["C","A"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140476685,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140476685,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795127521"},{"start":140476687,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140476687,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795127569","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476688,"feature_type":"variation","strand":1,"end":140476688,"alleles":["A","C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1238575017"},{"id":"rs1447153026","seq_region_name":"7","clinical_significance":[],"start":140476691,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140476691,"alleles":["A","-"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476693,"feature_type":"variation","strand":1,"end":140476693,"alleles":["A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs938316826"},{"seq_region_name":"7","id":"rs1795127820","clinical_significance":[],"strand":1,"feature_type":"variation","end":140476694,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476694,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1263428912","clinical_significance":[],"strand":1,"feature_type":"variation","end":140476695,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476695,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795127908","clinical_significance":[],"end":140476695,"alleles":["T","TCAGTAACTGAGTATCCTGTTCATGATACTCAGTAACTGAGTATCCTGTTAATGATAAT"],"strand":1,"feature_type":"variation","start":140476695,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795127965","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140476696,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476696,"source":"dbSNP"},{"end":140476709,"alleles":["GGAACTGAGGAAAG","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140476696,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795128014"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1206540029","feature_type":"variation","strand":1,"end":140476733,"alleles":["GGAACTGAGGAAAGAAACTGAGGAACTGAGGAAAGAAA","GGAACTGAGGAAAGAAA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476696},{"source":"dbSNP","start":140476697,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140476697,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs919521510","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795128176","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["AACTGAGGAAAGAAACTGAGGAA","AACTGAGGAA","AACTGAGGAAAGAAACTGAGGAAAGAAACTGAGGAA"],"end":140476720,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476698,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140476701,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476701,"clinical_significance":[],"seq_region_name":"7","id":"rs1795128246"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476702,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140476702,"seq_region_name":"7","id":"rs1464300189","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795128380","clinical_significance":[],"alleles":["G","A"],"end":140476704,"strand":1,"feature_type":"variation","start":140476704,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["A","C"],"end":140476706,"strand":1,"feature_type":"variation","start":140476706,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1055988432","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs778310370","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476708,"feature_type":"variation","strand":1,"end":140476708,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1285820717","feature_type":"variation","strand":1,"end":140476728,"alleles":["AACTGAGGAACTGAGGAA","AACTGAGGAA","AACTGAGGAACTGAGGAACTGAGGAA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476711},{"start":140476714,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140476715,"alleles":["TG","-"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1205541044","clinical_significance":[]},{"seq_region_name":"7","id":"rs950969733","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140476718,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476718,"source":"dbSNP"},{"end":140476721,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140476721,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795128971","clinical_significance":[]},{"end":140476727,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140476727,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795129035"},{"clinical_significance":[],"seq_region_name":"7","id":"rs894224178","source":"dbSNP","start":140476730,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140476730,"alleles":["G","A"],"feature_type":"variation","strand":1},{"end":140476733,"alleles":["A","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140476733,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs988118584"},{"source":"dbSNP","start":140476742,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140476742,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs567999863"},{"seq_region_name":"7","id":"rs535225690","clinical_significance":[],"start":140476744,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140476744,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1795129255","seq_region_name":"7","feature_type":"variation","strand":1,"end":140476745,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476745},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476749,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140476749,"seq_region_name":"7","id":"rs747473262","clinical_significance":[]},{"clinical_significance":[],"id":"rs941862675","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","-"],"end":140476749,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476749},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795129431","alleles":["G","C"],"end":140476751,"feature_type":"variation","strand":1,"source":"dbSNP","start":140476751,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476757,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140476757,"id":"rs2130373570","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140476759,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140476759,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130373580"},{"source":"dbSNP","start":140476760,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140476760,"alleles":["T","A","C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs943028252"},{"seq_region_name":"7","id":"rs2130373609","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476762,"source":"dbSNP","strand":1,"feature_type":"variation","end":140476762,"alleles":["T","C"]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140476766,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476766,"source":"dbSNP","id":"rs2130373621","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140476768,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476768,"clinical_significance":[],"seq_region_name":"7","id":"rs1487884255"},{"seq_region_name":"7","id":"rs2130373652","clinical_significance":[],"alleles":["G","A"],"end":140476770,"strand":1,"feature_type":"variation","start":140476770,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795129545","end":140476771,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140476771,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs897760255","seq_region_name":"7","feature_type":"variation","strand":1,"end":140476772,"alleles":["G","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476772},{"alleles":["C","T"],"end":140476773,"feature_type":"variation","strand":1,"source":"dbSNP","start":140476773,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795129665"},{"source":"dbSNP","start":140476775,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140476775,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs2130373724","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130373740","end":140476777,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140476777,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs993399936","seq_region_name":"7","end":140476779,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140476779,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140476780,"alleles":["T","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140476780,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1030191726"},{"end":140476799,"alleles":["GAACGATAAGGATCATAGA","GA"],"strand":1,"feature_type":"variation","start":140476781,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795129786","clinical_significance":[]},{"clinical_significance":[],"id":"rs2130373806","seq_region_name":"7","source":"dbSNP","start":140476782,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140476782,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs547125400","seq_region_name":"7","alleles":["C","G","T"],"end":140476784,"feature_type":"variation","strand":1,"source":"dbSNP","start":140476784,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["CGATAAGGATCATAGACCG","CGATAAGGATCATAGACCGATAAGGATCATAGACCG"],"end":140476802,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476784,"clinical_significance":[],"seq_region_name":"7","id":"rs1795129920"},{"feature_type":"variation","strand":1,"end":140476808,"alleles":["CGATAAGGATCATAGACCGGGTGCG","CG"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476784,"clinical_significance":[],"id":"rs1795129983","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1381591454","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476785,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140476785},{"seq_region_name":"7","id":"rs1475470480","clinical_significance":[],"end":140476787,"alleles":["T","TT"],"strand":1,"feature_type":"variation","start":140476787,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140476788,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140476788,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795130257","clinical_significance":[]},{"clinical_significance":[],"id":"rs1391591000","seq_region_name":"7","feature_type":"variation","strand":1,"end":140476795,"alleles":["AGGATCA","AGGATCACAGACCAGGATCA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476789},{"alleles":["AGGATCATAG","AG"],"end":140476798,"feature_type":"variation","strand":1,"source":"dbSNP","start":140476789,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795130369","seq_region_name":"7"},{"source":"dbSNP","start":140476790,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140476790,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795130431","seq_region_name":"7"},{"end":140476795,"alleles":["GGATCA","GGATCACAGACCGGATCA"],"strand":1,"feature_type":"variation","start":140476790,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795130481","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795130528","clinical_significance":[],"start":140476791,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140476790,"alleles":["-","T"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476791,"feature_type":"variation","strand":1,"end":140476791,"alleles":["G","A"],"clinical_significance":[],"id":"rs925664809","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476793,"source":"dbSNP","strand":1,"feature_type":"variation","end":140476793,"alleles":["T","A","C"],"seq_region_name":"7","id":"rs1186329081","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140476795,"alleles":["A","ACAGACCAGGA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476795,"clinical_significance":[],"seq_region_name":"7","id":"rs1795130692"},{"source":"dbSNP","start":140476795,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140476795,"alleles":["A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130373961"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476795,"feature_type":"variation","strand":1,"end":140476797,"alleles":["ATA","-"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795130751"},{"seq_region_name":"7","id":"rs17621391","clinical_significance":[],"strand":1,"feature_type":"variation","end":140476796,"alleles":["T","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476796,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795130927","clinical_significance":[],"end":140476796,"alleles":["-","CAC"],"strand":1,"feature_type":"variation","start":140476797,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795130996","source":"dbSNP","start":140476797,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AGA","AGAGA"],"end":140476799,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140476801,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476801,"clinical_significance":[],"seq_region_name":"7","id":"rs751443579"},{"seq_region_name":"7","id":"rs754882059","clinical_significance":[],"alleles":["G","A","C","T"],"end":140476802,"strand":1,"feature_type":"variation","start":140476802,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140476803,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140476803,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795131217","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795131265","feature_type":"variation","strand":1,"alleles":["GGTGCGGTG","GGTGCGGTGCGGTG"],"end":140476811,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476803},{"seq_region_name":"7","id":"rs570361442","clinical_significance":[],"start":140476807,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G","T"],"end":140476807,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs539492373","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140476808,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476808,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476809,"source":"dbSNP","strand":1,"feature_type":"variation","end":140476809,"alleles":["G","C"],"seq_region_name":"7","id":"rs557596517","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476810,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140476810,"clinical_significance":[],"seq_region_name":"7","id":"rs1795131522"},{"source":"dbSNP","start":140476812,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140476812,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1046057846"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1341607947","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140476813,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476813},{"seq_region_name":"7","id":"rs1348308264","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476816,"source":"dbSNP","strand":1,"feature_type":"variation","end":140476816,"alleles":["A","AA"]},{"id":"rs1440304536","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140476817,"alleles":["C","A","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476817,"source":"dbSNP"},{"id":"rs112912250","seq_region_name":"7","clinical_significance":[],"start":140476818,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140476818,"strand":1,"feature_type":"variation"},{"start":140476820,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140476820,"strand":1,"feature_type":"variation","id":"rs1795131930","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140476822,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140476822,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2099857623"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795131982","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476823,"feature_type":"variation","strand":1,"alleles":["TAATCCCAGCACTTTG","TAATCCCAGCACTTTGTAATCCCAGCACTTTG"],"end":140476838},{"feature_type":"variation","strand":1,"alleles":["TCCCAGCACTTT","-"],"end":140476837,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476826,"clinical_significance":[],"seq_region_name":"7","id":"rs1340343427"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1379182002","source":"dbSNP","start":140476827,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140476827,"alleles":["C","A","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795132166","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140476833,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476833,"source":"dbSNP"},{"start":140476834,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140476834,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs990065968","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795132278","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476838,"source":"dbSNP","strand":1,"feature_type":"variation","end":140476838,"alleles":["G","C"]},{"id":"rs1795132327","seq_region_name":"7","clinical_significance":[],"start":140476839,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140476839,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"alleles":["G","C"],"end":140476840,"strand":1,"feature_type":"variation","start":140476840,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795132419","clinical_significance":[]},{"id":"rs1021096094","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140476843,"strand":1,"feature_type":"variation","start":140476843,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476846,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140476846,"clinical_significance":[],"id":"rs2130374270","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1002172072","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476848,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140476848},{"seq_region_name":"7","id":"rs966851668","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476849,"source":"dbSNP","strand":1,"feature_type":"variation","end":140476849,"alleles":["G","A"]},{"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140476851,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476851,"source":"dbSNP","seq_region_name":"7","id":"rs1166322094","clinical_significance":[]},{"end":140476852,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140476852,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs536690045","seq_region_name":"7"},{"end":140476855,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140476855,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1445293596","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1471704755","feature_type":"variation","strand":1,"end":140476856,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476856},{"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140476857,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476857,"source":"dbSNP","seq_region_name":"7","id":"rs1309170777","clinical_significance":[]},{"end":140476864,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140476864,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795133294","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1236798547","source":"dbSNP","start":140476867,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140476867,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs982391887","clinical_significance":[],"alleles":["T","A"],"end":140476868,"strand":1,"feature_type":"variation","start":140476868,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1357507053","source":"dbSNP","start":140476869,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140476869,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1249796475","feature_type":"variation","strand":1,"end":140476870,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476870},{"clinical_significance":[],"seq_region_name":"7","id":"rs1230335984","feature_type":"variation","strand":1,"end":140476871,"alleles":["G","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476871},{"clinical_significance":[],"seq_region_name":"7","id":"rs1033766771","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140476875,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476875},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795134039","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476877,"feature_type":"variation","strand":1,"end":140476877,"alleles":["C","G","T"]},{"start":140476878,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140476878,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795134154","clinical_significance":[]},{"id":"rs963433580","seq_region_name":"7","clinical_significance":[],"alleles":["G","C"],"end":140476880,"strand":1,"feature_type":"variation","start":140476880,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140476885,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476885,"source":"dbSNP","id":"rs1795134328","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476887,"source":"dbSNP","strand":1,"feature_type":"variation","end":140476887,"alleles":["C","G","T"],"id":"rs756016515","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1226927360","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476889,"feature_type":"variation","strand":1,"end":140476889,"alleles":["G","-"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476889,"feature_type":"variation","strand":1,"end":140476889,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1356144378"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1320783743","source":"dbSNP","start":140476891,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140476891,"alleles":["C","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1280629866","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476894,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140476894},{"seq_region_name":"7","id":"rs995019959","clinical_significance":[],"start":140476895,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","T"],"end":140476895,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476896,"source":"dbSNP","strand":1,"feature_type":"variation","end":140476896,"alleles":["A","G"],"seq_region_name":"7","id":"rs928195377","clinical_significance":[]},{"start":140476897,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140476897,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs555241275","clinical_significance":[]},{"seq_region_name":"7","id":"rs959734985","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140476898,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476898,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476899,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140476899,"clinical_significance":[],"id":"rs1795135327","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795135410","clinical_significance":[],"strand":1,"feature_type":"variation","end":140476904,"alleles":["AAA","AAAA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476902,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476904,"feature_type":"variation","strand":1,"end":140476904,"alleles":["A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1365767283"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1166521906","source":"dbSNP","start":140476907,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140476907,"feature_type":"variation","strand":1},{"alleles":["G","A","T"],"end":140476909,"strand":1,"feature_type":"variation","start":140476909,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs145878319","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795135756","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","TT"],"end":140476910,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476910,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1795135843","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476911,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140476911},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795135921","source":"dbSNP","start":140476911,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["CTC","-"],"end":140476913,"feature_type":"variation","strand":1},{"end":140476917,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140476917,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795135996"},{"clinical_significance":[],"seq_region_name":"7","id":"rs915654885","feature_type":"variation","strand":1,"alleles":["T","A"],"end":140476923,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476923},{"clinical_significance":[],"id":"rs941762016","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476928,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140476928},{"feature_type":"variation","strand":1,"alleles":["TT","T"],"end":140476931,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476930,"clinical_significance":[],"seq_region_name":"7","id":"rs1795136074"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795136178","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140476931,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476931},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795136258","alleles":["A","T"],"end":140476932,"feature_type":"variation","strand":1,"source":"dbSNP","start":140476932,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795136342","alleles":["AGTCAG","AG"],"end":140476937,"feature_type":"variation","strand":1,"source":"dbSNP","start":140476932,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1795136432","seq_region_name":"7","alleles":["G","A"],"end":140476933,"feature_type":"variation","strand":1,"source":"dbSNP","start":140476933,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1473668596","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476940,"feature_type":"variation","strand":1,"end":140476940,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1409682386","clinical_significance":[],"start":140476944,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140476944,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1795136695","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476946,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140476946},{"clinical_significance":[],"seq_region_name":"7","id":"rs1181489884","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476948,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140476948},{"id":"rs1585502054","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140476953,"strand":1,"feature_type":"variation","start":140476953,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140476954,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140476954,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585502068"},{"seq_region_name":"7","id":"rs540978909","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140476955,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476955,"source":"dbSNP"},{"clinical_significance":[],"id":"rs748951818","seq_region_name":"7","source":"dbSNP","start":140476956,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140476956,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1412763266","clinical_significance":[],"start":140476957,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140476957,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs964347956","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476958,"source":"dbSNP","strand":1,"feature_type":"variation","end":140476958,"alleles":["C","T"]},{"clinical_significance":[],"id":"rs1451385000","seq_region_name":"7","alleles":["T","C"],"end":140476961,"feature_type":"variation","strand":1,"source":"dbSNP","start":140476961,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140476962,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476962,"source":"dbSNP","seq_region_name":"7","id":"rs974353839","clinical_significance":[]},{"clinical_significance":[],"id":"rs1051669974","seq_region_name":"7","source":"dbSNP","start":140476964,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140476964,"alleles":["T","A","C"],"feature_type":"variation","strand":1},{"start":140476965,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140476965,"strand":1,"feature_type":"variation","id":"rs1250050614","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795137794","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140476966,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476966,"source":"dbSNP"},{"alleles":["C","A"],"end":140476967,"strand":1,"feature_type":"variation","start":140476967,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1288301795","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795137963","end":140476968,"alleles":["A","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140476968,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140476969,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476969,"clinical_significance":[],"seq_region_name":"7","id":"rs1345647843"},{"seq_region_name":"7","id":"rs1464072985","clinical_significance":[],"strand":1,"feature_type":"variation","end":140476969,"alleles":["G","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476969,"source":"dbSNP"},{"id":"rs1795138798","seq_region_name":"7","clinical_significance":[],"alleles":["C","G"],"end":140476970,"strand":1,"feature_type":"variation","start":140476970,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140476971,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476971,"clinical_significance":[],"seq_region_name":"7","id":"rs1795138898"},{"source":"dbSNP","start":140476978,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140476978,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs925716270"},{"strand":1,"feature_type":"variation","end":140476979,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476979,"source":"dbSNP","id":"rs890331533","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795139186","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476981,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140476981},{"alleles":["G","A"],"end":140476984,"strand":1,"feature_type":"variation","start":140476984,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1007979238","clinical_significance":[]},{"clinical_significance":[],"id":"rs1318659560","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476986,"feature_type":"variation","strand":1,"end":140476986,"alleles":["A","G"]},{"source":"dbSNP","start":140476987,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140476987,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795139458"},{"end":140476994,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140476994,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1386314882"},{"id":"rs1458639250","seq_region_name":"7","clinical_significance":[],"start":140476994,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","AA"],"end":140476994,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140476995,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140476995,"source":"dbSNP","seq_region_name":"7","id":"rs1158391801","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140476998,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140476998,"clinical_significance":[],"seq_region_name":"7","id":"rs866132289"},{"alleles":["G","A"],"end":140477001,"feature_type":"variation","strand":1,"source":"dbSNP","start":140477001,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1427431045"},{"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140477002,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477002,"source":"dbSNP","id":"rs1052784234","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477003,"feature_type":"variation","strand":1,"end":140477003,"alleles":["C","T"],"clinical_significance":[],"id":"rs913102516","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs188249481","alleles":["G","A"],"end":140477005,"feature_type":"variation","strand":1,"source":"dbSNP","start":140477005,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1210924914","seq_region_name":"7","end":140477006,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140477006,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1021039439","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477008,"feature_type":"variation","strand":1,"end":140477008,"alleles":["G","C","T"]},{"seq_region_name":"7","id":"rs1268028108","clinical_significance":[],"strand":1,"feature_type":"variation","end":140477018,"alleles":["AATTAA","AA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477013,"source":"dbSNP"},{"source":"dbSNP","start":140477014,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140477014,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs966903843"},{"feature_type":"variation","strand":1,"end":140477015,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477015,"clinical_significance":[],"seq_region_name":"7","id":"rs1312259583"},{"seq_region_name":"7","id":"rs1795141568","clinical_significance":[],"start":140477020,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140477020,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs577780914","clinical_significance":[],"start":140477024,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140477024,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1216983521","feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140477025,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477025},{"alleles":["G","A"],"end":140477028,"feature_type":"variation","strand":1,"source":"dbSNP","start":140477028,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1259587275"},{"seq_region_name":"7","id":"rs1366410836","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140477029,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477029,"source":"dbSNP"},{"end":140477030,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140477030,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs949914966","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795142128","source":"dbSNP","start":140477034,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140477034,"alleles":["G","A"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477035,"source":"dbSNP","strand":1,"feature_type":"variation","end":140477035,"alleles":["T","C","G"],"id":"rs1585502274","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140477036,"alleles":["TT","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477035,"source":"dbSNP","seq_region_name":"7","id":"rs1197433204","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140477038,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477038,"clinical_significance":[],"id":"rs1386250694","seq_region_name":"7"},{"start":140477039,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140477039,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1319796953","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795142595","clinical_significance":[],"start":140477040,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140477040,"alleles":["G","A","T"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477041,"feature_type":"variation","strand":1,"alleles":["T","TT"],"end":140477041,"clinical_significance":[],"id":"rs1470303256","seq_region_name":"7"},{"seq_region_name":"7","id":"rs2130375266","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477045,"source":"dbSNP","strand":1,"feature_type":"variation","end":140477044,"alleles":["-","CCT"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1360837703","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140477045,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477045},{"source":"dbSNP","start":140477046,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140477046,"alleles":["A","AA"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1173978968"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130375307","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477046,"feature_type":"variation","strand":1,"end":140477048,"alleles":["AGA","-"]},{"alleles":["AGAGA","AGA"],"end":140477050,"strand":1,"feature_type":"variation","start":140477046,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1414005553","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477050,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140477050,"clinical_significance":[],"id":"rs545461129","seq_region_name":"7"},{"end":140477054,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140477054,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130375343","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130375355","clinical_significance":[],"strand":1,"feature_type":"variation","end":140477055,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477055,"source":"dbSNP"},{"id":"rs905737814","seq_region_name":"7","clinical_significance":[],"start":140477058,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140477058,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"id":"rs2130375373","seq_region_name":"7","clinical_significance":[],"start":140477059,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140477059,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1795143253","clinical_significance":[],"end":140477064,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140477064,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477065,"source":"dbSNP","strand":1,"feature_type":"variation","end":140477065,"alleles":["T","C"],"seq_region_name":"7","id":"rs938012921","clinical_significance":[]},{"alleles":["C","A","T"],"end":140477066,"strand":1,"feature_type":"variation","start":140477066,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795143443","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795143553","end":140477067,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140477067,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140477070,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140477070,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs375822760","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477073,"feature_type":"variation","strand":1,"end":140477073,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1184597567"},{"clinical_significance":[],"id":"rs1448028932","seq_region_name":"7","source":"dbSNP","start":140477073,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140477075,"alleles":["GGG","GG"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477073,"source":"dbSNP","strand":1,"feature_type":"variation","end":140477090,"alleles":["GGGAAACAAGAGGGAAAC","GGGAAAC"],"id":"rs1247866652","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140477074,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477074,"source":"dbSNP","seq_region_name":"7","id":"rs1795144003","clinical_significance":[]},{"id":"rs2130375462","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477076,"source":"dbSNP","strand":1,"feature_type":"variation","end":140477076,"alleles":["A","T"]},{"end":140477077,"alleles":["A","G","T"],"strand":1,"feature_type":"variation","start":140477077,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795144099","clinical_significance":[]},{"alleles":["A","T"],"end":140477078,"feature_type":"variation","strand":1,"source":"dbSNP","start":140477078,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795144173"},{"seq_region_name":"7","id":"rs980698485","clinical_significance":[],"strand":1,"feature_type":"variation","end":140477079,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477079,"source":"dbSNP"},{"seq_region_name":"7","id":"rs2130375502","clinical_significance":[],"alleles":["AA","A"],"end":140477081,"strand":1,"feature_type":"variation","start":140477080,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140477082,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477082,"source":"dbSNP","id":"rs1795144367","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477083,"source":"dbSNP","strand":1,"feature_type":"variation","end":140477083,"alleles":["A","T"],"seq_region_name":"7","id":"rs1795144465","clinical_significance":[]},{"seq_region_name":"7","id":"rs1185263674","clinical_significance":[],"strand":1,"feature_type":"variation","end":140477084,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477084,"source":"dbSNP"},{"end":140477085,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140477085,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130375547"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1484491884","source":"dbSNP","start":140477086,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140477086,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs2130375567","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477088,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140477088},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477090,"feature_type":"variation","strand":1,"alleles":["CTCT","CT"],"end":140477093,"clinical_significance":[],"id":"rs553319517","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585502377","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140477091,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477091},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795144754","feature_type":"variation","strand":1,"end":140477093,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477093},{"feature_type":"variation","strand":1,"end":140477094,"alleles":["G","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477094,"clinical_significance":[],"seq_region_name":"7","id":"rs2130375620"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477095,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140477095,"id":"rs1477985423","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1311148473","end":140477096,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140477096,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["T","A"],"end":140477097,"strand":1,"feature_type":"variation","start":140477097,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1429574370","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477098,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["-","A","AA","AAA","AAAA"],"end":140477097,"seq_region_name":"7","id":"rs1795144912","clinical_significance":[]},{"start":140477098,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140477098,"alleles":["C","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1309009446","clinical_significance":[]},{"end":140477098,"alleles":["C","-"],"strand":1,"feature_type":"variation","start":140477098,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795145064","clinical_significance":[]},{"source":"dbSNP","start":140477098,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140477099,"alleles":["CA","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795145117"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477099,"source":"dbSNP","strand":1,"feature_type":"variation","end":140477117,"alleles":["AAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAA","AAAAAAAAAAAAA","AAAAAAAAAAAAAA","AAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAA"],"id":"rs35476052","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795145495","source":"dbSNP","start":140477101,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140477101,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs2130375774","clinical_significance":[],"alleles":["A","G"],"end":140477103,"strand":1,"feature_type":"variation","start":140477103,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130375783","feature_type":"variation","strand":1,"end":140477105,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477105},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585502430","source":"dbSNP","start":140477109,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140477109,"alleles":["A","AGA"],"feature_type":"variation","strand":1},{"alleles":["A","G"],"end":140477115,"feature_type":"variation","strand":1,"source":"dbSNP","start":140477115,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130375802"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477116,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AAT","-"],"end":140477118,"seq_region_name":"7","id":"rs1795145607","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795145657","clinical_significance":[],"strand":1,"feature_type":"variation","end":140477116,"alleles":["-","TG"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477117,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477117,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AT","-"],"end":140477118,"id":"rs2130375844","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs60553667","clinical_significance":[],"strand":1,"feature_type":"variation","end":140477118,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477118,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs202132256","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477118,"feature_type":"variation","strand":1,"end":140477118,"alleles":["T","-"]},{"seq_region_name":"7","id":"rs1795145825","clinical_significance":[],"alleles":["TG","-"],"end":140477119,"strand":1,"feature_type":"variation","start":140477118,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140477119,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140477119,"alleles":["G","A","C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585502447","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1389798492","feature_type":"variation","strand":1,"end":140477120,"alleles":["A","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477120},{"start":140477120,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140477120,"alleles":["A","AAAA"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1788933954","clinical_significance":[]},{"source":"dbSNP","start":140477121,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140477121,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1476907776"},{"start":140477124,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140477124,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1055103349","clinical_significance":[]},{"source":"dbSNP","start":140477125,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140477140,"alleles":["TGACATTCCTCTATCT","TGACATTCCTCTATCTCCTGACATTCCTCTATCT"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795146122"},{"end":140477127,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140477127,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1402944488","clinical_significance":[]},{"alleles":["A","C"],"end":140477129,"strand":1,"feature_type":"variation","start":140477129,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795146232","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477133,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CTCT","CTCTCT"],"end":140477136,"seq_region_name":"7","id":"rs1254652427","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795146331","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477134,"source":"dbSNP","strand":1,"feature_type":"variation","end":140477141,"alleles":["TCTATCTA","TCTA"]},{"feature_type":"variation","strand":1,"end":140477135,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477135,"clinical_significance":[],"seq_region_name":"7","id":"rs899153526"},{"clinical_significance":[],"id":"rs1416670592","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477138,"feature_type":"variation","strand":1,"end":140477138,"alleles":["T","A"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477138,"feature_type":"variation","strand":1,"end":140477144,"alleles":["TCTAAAG","TCTAAAGTCTAAAG"],"clinical_significance":[],"id":"rs1795146582","seq_region_name":"7"},{"id":"rs1482637663","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477139,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140477139},{"clinical_significance":[],"id":"rs1795146940","seq_region_name":"7","end":140477143,"alleles":["AAA","AAAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140477141,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140477143,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140477143,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs994948877","clinical_significance":[]},{"end":140477144,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140477144,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1251820908","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477145,"feature_type":"variation","strand":1,"end":140477145,"alleles":["G","A"],"clinical_significance":[],"id":"rs1206671485","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1026815493","end":140477146,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140477146,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140477150,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477150,"clinical_significance":[],"id":"rs1795147368","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs991576669","source":"dbSNP","start":140477152,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140477152,"alleles":["T","A","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1245288621","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477157,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140477157},{"clinical_significance":[],"id":"rs915556250","seq_region_name":"7","alleles":["TAAGTAAG","TAAG"],"end":140477165,"feature_type":"variation","strand":1,"source":"dbSNP","start":140477158,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1795147754","seq_region_name":"7","source":"dbSNP","start":140477159,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AA","AAA"],"end":140477160,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs963361318","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477163,"feature_type":"variation","strand":1,"end":140477163,"alleles":["A","T"]},{"id":"rs563663692","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477164,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140477164},{"source":"dbSNP","start":140477167,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140477167,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs756787637"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795148134","feature_type":"variation","strand":1,"end":140477168,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477168},{"seq_region_name":"7","id":"rs1795148229","clinical_significance":[],"start":140477170,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140477170,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1332695867","seq_region_name":"7","source":"dbSNP","start":140477173,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140477173,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140477174,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140477174,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1309999207"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477175,"feature_type":"variation","strand":1,"end":140477178,"alleles":["TGGT","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1375295089"},{"end":140477176,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140477176,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs59923382","clinical_significance":[]},{"start":140477177,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140477177,"alleles":["G","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795148846","clinical_significance":[]},{"start":140477180,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140477180,"alleles":["C","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1009438417","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140477181,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477181,"source":"dbSNP","seq_region_name":"7","id":"rs1795149001","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1294297803","feature_type":"variation","strand":1,"alleles":["AACAAC","AAC"],"end":140477190,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477185},{"seq_region_name":"7","id":"rs1795149116","clinical_significance":[],"alleles":["A","G"],"end":140477186,"strand":1,"feature_type":"variation","start":140477186,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140477187,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477187,"clinical_significance":[],"seq_region_name":"7","id":"rs1459787133"},{"strand":1,"feature_type":"variation","end":140477190,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477190,"source":"dbSNP","seq_region_name":"7","id":"rs919003511","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477191,"source":"dbSNP","strand":1,"feature_type":"variation","end":140477191,"alleles":["C","A","G","T"],"seq_region_name":"7","id":"rs77927479","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140477192,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477192,"source":"dbSNP","seq_region_name":"7","id":"rs964900897","clinical_significance":[]},{"id":"rs1274949375","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140477198,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477198,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795149490","clinical_significance":[],"start":140477202,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140477202,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795149555","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477204,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140477204},{"id":"rs1795149614","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477208,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140477208},{"end":140477209,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140477209,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130376367","clinical_significance":[]},{"start":140477211,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140477211,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs911820627","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477214,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140477214,"clinical_significance":[],"seq_region_name":"7","id":"rs1795149740"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477215,"source":"dbSNP","strand":1,"feature_type":"variation","end":140477215,"alleles":["C","T"],"id":"rs1210006247","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140477216,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477216,"source":"dbSNP","seq_region_name":"7","id":"rs974950251","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795149905","source":"dbSNP","start":140477217,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140477217,"alleles":["C","T"],"feature_type":"variation","strand":1},{"start":140477218,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140477218,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1346431869","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs776015475","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477219,"feature_type":"variation","strand":1,"end":140477219,"alleles":["A","T"]},{"alleles":["G","A"],"end":140477220,"feature_type":"variation","strand":1,"source":"dbSNP","start":140477220,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs10441209"},{"clinical_significance":[],"seq_region_name":"7","id":"rs561269207","end":140477222,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140477222,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1198664305","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477225,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140477225},{"clinical_significance":[],"seq_region_name":"7","id":"rs528755093","end":140477231,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140477231,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140477232,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477232,"clinical_significance":[],"id":"rs1795150197","seq_region_name":"7"},{"seq_region_name":"7","id":"rs912939959","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A","G"],"end":140477234,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477234,"source":"dbSNP"},{"id":"rs1290104430","seq_region_name":"7","clinical_significance":[],"start":140477236,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140477236,"alleles":["T","A","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1226683917","seq_region_name":"7","end":140477245,"alleles":["ACAACAA","ACAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140477239,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1349893371","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477244,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AATAA","AA"],"end":140477248},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795150534","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477246,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140477246},{"seq_region_name":"7","id":"rs146644993","clinical_significance":[],"strand":1,"feature_type":"variation","end":140477247,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477247,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1488525284","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477247,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AAAAAA","AAAAA"],"end":140477252},{"seq_region_name":"7","id":"rs1388670377","clinical_significance":[],"alleles":["A","C"],"end":140477251,"strand":1,"feature_type":"variation","start":140477251,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140477254,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140477254,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795150800","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477256,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140477256,"seq_region_name":"7","id":"rs1795150857","clinical_significance":[]},{"clinical_significance":[],"id":"rs1388839054","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477261,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140477261},{"source":"dbSNP","start":140477262,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140477262,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs893837831"},{"seq_region_name":"7","id":"rs571791048","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140477268,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477268,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140477271,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477271,"source":"dbSNP","seq_region_name":"7","id":"rs1391514793","clinical_significance":[]},{"source":"dbSNP","start":140477271,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140477271,"alleles":["A","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795151126"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477273,"feature_type":"variation","strand":1,"end":140477273,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585502733"},{"clinical_significance":[],"id":"rs1157529573","seq_region_name":"7","source":"dbSNP","start":140477274,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140477274,"feature_type":"variation","strand":1},{"start":140477275,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140477280,"alleles":["AAAAAA","AAAAA"],"strand":1,"feature_type":"variation","id":"rs1795151335","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140477276,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140477276,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795151384","seq_region_name":"7"},{"end":140477280,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140477280,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585502748"},{"seq_region_name":"7","id":"rs538897208","clinical_significance":[],"start":140477281,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140477281,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140477281,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["CCCCC","CCCC","CCCCCC"],"end":140477285,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1471333643"},{"seq_region_name":"7","id":"rs1042537100","clinical_significance":[],"start":140477282,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140477282,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs902562392","clinical_significance":[],"end":140477285,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140477285,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140477286,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140477286,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs79767534"},{"seq_region_name":"7","id":"rs1795151800","clinical_significance":[],"start":140477287,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140477287,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795151851","end":140477288,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140477288,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140477291,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140477291,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs937271889","clinical_significance":[]},{"start":140477292,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140477292,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs569460906","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs899205376","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140477295,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477295},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795152061","source":"dbSNP","start":140477297,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140477297,"alleles":["A","T"],"feature_type":"variation","strand":1},{"end":140477302,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140477302,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1563099015"},{"start":140477304,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140477304,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795152177","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140477305,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477305,"clinical_significance":[],"seq_region_name":"7","id":"rs1795152236"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1328582919","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477306,"feature_type":"variation","strand":1,"end":140477306,"alleles":["T","C","G"]},{"seq_region_name":"7","id":"rs1206676912","clinical_significance":[],"start":140477306,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140477324,"alleles":["TCTTTCTTTTCTTTCTTTT","TCTTTCTTTT"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1795152444","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140477307,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477307,"source":"dbSNP"},{"end":140477308,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140477308,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1275580852","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1235494271","alleles":["T","C"],"end":140477309,"feature_type":"variation","strand":1,"source":"dbSNP","start":140477309,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140477312,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140477315,"alleles":["TTTT","-"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1329611571","clinical_significance":[]},{"start":140477313,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TTTCTTTCTTT","TTTCTTT"],"end":140477323,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1378284212","clinical_significance":[]},{"start":140477317,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140477317,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795152727","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477317,"source":"dbSNP","strand":1,"feature_type":"variation","end":140477319,"alleles":["TTT","TTTT"],"seq_region_name":"7","id":"rs1795152792","clinical_significance":[]},{"clinical_significance":[],"id":"rs1436310494","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477317,"feature_type":"variation","strand":1,"alleles":["TTTCTTTTT","-"],"end":140477325},{"source":"dbSNP","start":140477317,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140477330,"alleles":["TTTCTTTTTCTTTT","TTT"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1367725461","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795152960","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477319,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140477319},{"end":140477320,"alleles":["C","A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140477320,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795153014"},{"source":"dbSNP","start":140477321,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TTTTT","T"],"end":140477325,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1479046765"},{"feature_type":"variation","strand":1,"end":140477324,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477324,"clinical_significance":[],"id":"rs1171398125","seq_region_name":"7"},{"alleles":["T","C"],"end":140477330,"feature_type":"variation","strand":1,"source":"dbSNP","start":140477330,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795153203"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477332,"feature_type":"variation","strand":1,"end":140477334,"alleles":["TGT","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs869113475"},{"clinical_significance":[],"seq_region_name":"7","id":"rs11353146","alleles":["G","-"],"end":140477333,"feature_type":"variation","strand":1,"source":"dbSNP","start":140477333,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477333,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140477333,"id":"rs63284260","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs200509710","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477333,"source":"dbSNP","strand":1,"feature_type":"variation","end":140477333,"alleles":["G","GG"]},{"seq_region_name":"7","id":"rs1795153517","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477334,"source":"dbSNP","strand":1,"feature_type":"variation","end":140477338,"alleles":["TTTTT","TTTT"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477337,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140477337,"clinical_significance":[],"id":"rs76569765","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1358968872","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477339,"feature_type":"variation","strand":1,"end":140477339,"alleles":["C","T"]},{"source":"dbSNP","start":140477341,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140477341,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1375603840"},{"clinical_significance":[],"id":"rs1323730210","seq_region_name":"7","source":"dbSNP","start":140477344,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140477344,"alleles":["G","C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1192562068","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140477346,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477346},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477347,"feature_type":"variation","strand":1,"end":140477350,"alleles":["AGAG","AG"],"clinical_significance":[],"seq_region_name":"7","id":"rs374383608"},{"id":"rs1795153982","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140477351,"strand":1,"feature_type":"variation","start":140477351,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477356,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140477356,"clinical_significance":[],"seq_region_name":"7","id":"rs1795154037"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477359,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140477359,"clinical_significance":[],"id":"rs1017596868","seq_region_name":"7"},{"id":"rs1795154172","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140477360,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477360,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1047809999","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140477361,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477361},{"id":"rs886498753","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477368,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140477368},{"clinical_significance":[],"id":"rs1795154400","seq_region_name":"7","source":"dbSNP","start":140477370,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["-","CCA"],"end":140477369,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs141442776","clinical_significance":[],"strand":1,"feature_type":"variation","end":140477374,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477374,"source":"dbSNP"},{"end":140477378,"alleles":["GAAG","GAAGCGAAG"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140477375,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1464430767","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1279212146","alleles":["A","T"],"end":140477376,"feature_type":"variation","strand":1,"source":"dbSNP","start":140477376,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140477377,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140477377,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1202285441","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477378,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140477378,"seq_region_name":"7","id":"rs1342904820","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795154830","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477382,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140477382},{"seq_region_name":"7","id":"rs1302638146","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477384,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140477384},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795155048","end":140477385,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140477385,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1354368225","feature_type":"variation","strand":1,"end":140477387,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477387},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795155257","alleles":["A","G"],"end":140477388,"feature_type":"variation","strand":1,"source":"dbSNP","start":140477388,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs192784159","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477389,"feature_type":"variation","strand":1,"end":140477389,"alleles":["T","A","C"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477397,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140477397,"clinical_significance":[],"seq_region_name":"7","id":"rs1283642853"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140477398,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477398,"source":"dbSNP","seq_region_name":"7","id":"rs973003502","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140477399,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477399,"clinical_significance":[],"seq_region_name":"7","id":"rs1434798456"},{"end":140477402,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140477402,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1563099101"},{"seq_region_name":"7","id":"rs1485385117","clinical_significance":[],"alleles":["C","T"],"end":140477403,"strand":1,"feature_type":"variation","start":140477403,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795155929","clinical_significance":[],"end":140477404,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140477404,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140477407,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140477407,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795156021","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477408,"source":"dbSNP","strand":1,"feature_type":"variation","end":140477408,"alleles":["G","A","C"],"seq_region_name":"7","id":"rs1336672931","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795156204","clinical_significance":[],"start":140477409,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140477409,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1397293054","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477413,"source":"dbSNP","strand":1,"feature_type":"variation","end":140477413,"alleles":["C","A","G"]},{"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140477414,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477414,"source":"dbSNP","seq_region_name":"7","id":"rs2130377402","clinical_significance":[]},{"id":"rs1795156423","seq_region_name":"7","clinical_significance":[],"alleles":["G","C"],"end":140477417,"strand":1,"feature_type":"variation","start":140477417,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1585503056","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140477418,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477418,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1399362962","feature_type":"variation","strand":1,"end":140477419,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477419},{"start":140477422,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140477422,"alleles":["A","C"],"strand":1,"feature_type":"variation","id":"rs1019558341","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795156782","clinical_significance":[],"alleles":["G","A"],"end":140477423,"strand":1,"feature_type":"variation","start":140477423,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477424,"source":"dbSNP","strand":1,"feature_type":"variation","end":140477424,"alleles":["C","A","G"],"seq_region_name":"7","id":"rs900660819","clinical_significance":[]},{"seq_region_name":"7","id":"rs1430081365","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477427,"source":"dbSNP","strand":1,"feature_type":"variation","end":140477427,"alleles":["C","T"]},{"end":140477429,"alleles":["CTC","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140477427,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1204844710"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795157135","end":140477429,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140477429,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140477430,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477430,"clinical_significance":[],"seq_region_name":"7","id":"rs534887233"},{"end":140477432,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140477432,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1033215715","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477432,"feature_type":"variation","strand":1,"alleles":["TG","TGTG"],"end":140477433,"clinical_significance":[],"seq_region_name":"7","id":"rs1391613734"},{"source":"dbSNP","start":140477434,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140477434,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585503091"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140477437,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477437,"clinical_significance":[],"id":"rs1268303416","seq_region_name":"7"},{"alleles":["A","C"],"end":140477438,"strand":1,"feature_type":"variation","start":140477438,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1253180581","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs957042253","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477439,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140477439},{"seq_region_name":"7","id":"rs1166531681","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477440,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140477440},{"start":140477441,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140477441,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795157998","clinical_significance":[]},{"seq_region_name":"7","id":"rs1026026169","clinical_significance":[],"start":140477443,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140477443,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"alleles":["C","A","T"],"end":140477444,"strand":1,"feature_type":"variation","start":140477444,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1238009874","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477445,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140477445,"clinical_significance":[],"seq_region_name":"7","id":"rs988843898"},{"seq_region_name":"7","id":"rs1795158393","clinical_significance":[],"start":140477448,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140477448,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1795158452","clinical_significance":[],"strand":1,"feature_type":"variation","end":140477449,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477449,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140477451,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477451,"clinical_significance":[],"seq_region_name":"7","id":"rs1795158719"},{"seq_region_name":"7","id":"rs1256989225","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140477452,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477452,"source":"dbSNP"},{"id":"rs769063050","seq_region_name":"7","clinical_significance":[],"start":140477455,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140477455,"alleles":["A","G","T"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["AGA","-"],"end":140477457,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477455,"clinical_significance":[],"id":"rs1196807078","seq_region_name":"7"},{"start":140477455,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AGATTA","-"],"end":140477460,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1205944162","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795159017","clinical_significance":[],"start":140477456,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140477456,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140477461,"alleles":["TAC","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477459,"source":"dbSNP","seq_region_name":"7","id":"rs1252410121","clinical_significance":[]},{"clinical_significance":[],"id":"rs1020050631","seq_region_name":"7","feature_type":"variation","strand":1,"end":140477461,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477461},{"clinical_significance":[],"id":"rs1795159202","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477462,"feature_type":"variation","strand":1,"alleles":["AA","A"],"end":140477463},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140477464,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477464,"clinical_significance":[],"id":"rs950440451","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795159321","feature_type":"variation","strand":1,"end":140477465,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477465},{"seq_region_name":"7","id":"rs971526916","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477466,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140477466},{"end":140477475,"alleles":["CCTGTCACC","CC"],"strand":1,"feature_type":"variation","start":140477467,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130377810","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795159445","source":"dbSNP","start":140477469,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140477469,"alleles":["T","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795159511","clinical_significance":[],"alleles":["G","A"],"end":140477470,"strand":1,"feature_type":"variation","start":140477470,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs981202852","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140477472,"strand":1,"feature_type":"variation","start":140477472,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140477474,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140477474,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795159604"},{"start":140477475,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140477475,"strand":1,"feature_type":"variation","id":"rs1228170078","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477477,"feature_type":"variation","strand":1,"end":140477477,"alleles":["C","T"],"clinical_significance":[],"id":"rs772881377","seq_region_name":"7"},{"end":140477478,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140477478,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1378855744","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs937157083","feature_type":"variation","strand":1,"end":140477479,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477479},{"clinical_significance":[],"id":"rs1795159891","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477480,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140477480},{"id":"rs1243166852","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140477481,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477481,"source":"dbSNP"},{"seq_region_name":"7","id":"rs553017556","clinical_significance":[],"start":140477482,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C","T"],"end":140477482,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs974022829","feature_type":"variation","strand":1,"end":140477488,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477488},{"source":"dbSNP","start":140477489,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140477489,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795160123","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1311804588","clinical_significance":[],"end":140477495,"alleles":["TTTTTT","TTTTTTT"],"strand":1,"feature_type":"variation","start":140477490,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs577749075","clinical_significance":[],"strand":1,"feature_type":"variation","end":140477491,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477491,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1409876143","source":"dbSNP","start":140477493,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140477493,"alleles":["T","C","G"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140477497,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477497,"clinical_significance":[],"id":"rs1372062343","seq_region_name":"7"},{"seq_region_name":"7","id":"rs919810169","clinical_significance":[],"start":140477498,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140477498,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140477503,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140477503,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130378051"},{"end":140477506,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140477506,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130378063"},{"seq_region_name":"7","id":"rs911748394","clinical_significance":[],"strand":1,"feature_type":"variation","end":140477508,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477508,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140477510,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477510,"clinical_significance":[],"seq_region_name":"7","id":"rs930676854"},{"source":"dbSNP","start":140477512,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140477512,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795160636","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1384680023","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140477513,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477513},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477515,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140477515,"clinical_significance":[],"seq_region_name":"7","id":"rs1471804655"},{"clinical_significance":[],"id":"rs1048160785","seq_region_name":"7","source":"dbSNP","start":140477517,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140477517,"alleles":["T","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs907855325","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140477522,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477522},{"alleles":["C","G"],"end":140477526,"strand":1,"feature_type":"variation","start":140477526,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs544913585","clinical_significance":[]},{"id":"rs1183039567","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477527,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140477527},{"clinical_significance":[],"id":"rs1795161071","seq_region_name":"7","end":140477528,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140477528,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795161137","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477529,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140477529},{"clinical_significance":[],"id":"rs567966215","seq_region_name":"7","feature_type":"variation","strand":1,"end":140477530,"alleles":["GG","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477529},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477532,"source":"dbSNP","strand":1,"feature_type":"variation","end":140477532,"alleles":["C","T"],"seq_region_name":"7","id":"rs535503782","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795161366","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140477533,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477533,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477536,"feature_type":"variation","strand":1,"end":140477536,"alleles":["C","T"],"clinical_significance":[],"id":"rs1040432353","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140477538,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477538,"source":"dbSNP","seq_region_name":"7","id":"rs563768192","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795161672","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140477539,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477539},{"seq_region_name":"7","id":"rs1585503275","clinical_significance":[],"alleles":["T","G"],"end":140477540,"strand":1,"feature_type":"variation","start":140477540,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140477543,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477543,"clinical_significance":[],"seq_region_name":"7","id":"rs900713374"},{"seq_region_name":"7","id":"rs1795161950","clinical_significance":[],"start":140477544,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140477544,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1563099218","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477546,"source":"dbSNP","strand":1,"feature_type":"variation","end":140477546,"alleles":["G","C"]},{"clinical_significance":[],"id":"rs1245217751","seq_region_name":"7","source":"dbSNP","start":140477554,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140477554,"alleles":["C","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1356318090","clinical_significance":[],"end":140477555,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140477555,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs183594507","clinical_significance":[],"start":140477556,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140477556,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"alleles":["C","T"],"end":140477563,"feature_type":"variation","strand":1,"source":"dbSNP","start":140477563,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs902614668"},{"id":"rs1585503328","seq_region_name":"7","clinical_significance":[],"alleles":["A","C"],"end":140477565,"strand":1,"feature_type":"variation","start":140477565,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140477566,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140477566,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585503332"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477567,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140477567,"seq_region_name":"7","id":"rs939393668","clinical_significance":[]},{"end":140477568,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","start":140477568,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1212003687","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140477573,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140477573,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1054638457"},{"feature_type":"variation","strand":1,"alleles":["GCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACTGTGCCCGGCCTAATTTTTGTATTCTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCCTTACCTCAGGCGATCCGCCCGCCTCAGCCTCCCAAA","GCCTCCCAAA"],"end":140477720,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477575,"clinical_significance":[],"seq_region_name":"7","id":"rs1563099237"},{"id":"rs1795163128","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477576,"source":"dbSNP","strand":1,"feature_type":"variation","end":140477576,"alleles":["C","T"]},{"clinical_significance":[],"id":"rs893365831","seq_region_name":"7","end":140477578,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140477578,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1286080979","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477579,"source":"dbSNP","strand":1,"feature_type":"variation","end":140477579,"alleles":["C","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795163408","feature_type":"variation","strand":1,"end":140477582,"alleles":["A","C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477582},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140477584,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477584,"source":"dbSNP","seq_region_name":"7","id":"rs1056545009","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140477585,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477585,"source":"dbSNP","seq_region_name":"7","id":"rs1350098900","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477587,"source":"dbSNP","strand":1,"feature_type":"variation","end":140477587,"alleles":["G","T"],"seq_region_name":"7","id":"rs1458216347","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140477590,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477590,"clinical_significance":[],"seq_region_name":"7","id":"rs1403360474"},{"seq_region_name":"7","id":"rs1181129028","clinical_significance":[],"start":140477591,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140477591,"alleles":["G","A","C"],"strand":1,"feature_type":"variation"},{"end":140477592,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140477592,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1159753760"},{"start":140477596,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140477596,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs895349882","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140477598,"alleles":["A","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477598,"source":"dbSNP","seq_region_name":"7","id":"rs1236867366","clinical_significance":[]},{"clinical_significance":[],"id":"rs776904077","seq_region_name":"7","source":"dbSNP","start":140477599,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140477599,"alleles":["G","C"],"feature_type":"variation","strand":1},{"end":140477601,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140477601,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1418907615","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1188637423","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477602,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140477602},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477604,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140477604,"clinical_significance":[],"seq_region_name":"7","id":"rs1020400247"},{"clinical_significance":[],"id":"rs971071376","seq_region_name":"7","source":"dbSNP","start":140477606,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140477606,"alleles":["G","A"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477613,"source":"dbSNP","strand":1,"feature_type":"variation","end":140477613,"alleles":["T","A"],"seq_region_name":"7","id":"rs1795164618","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140477614,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477614,"source":"dbSNP","seq_region_name":"7","id":"rs1012826775","clinical_significance":[]},{"seq_region_name":"7","id":"rs1017188241","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477615,"source":"dbSNP","strand":1,"feature_type":"variation","end":140477615,"alleles":["C","A","G"]},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140477618,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477618,"clinical_significance":[],"seq_region_name":"7","id":"rs1795164754"},{"clinical_significance":[],"seq_region_name":"7","id":"rs557288780","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140477623,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477623},{"source":"dbSNP","start":140477624,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140477624,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795164877"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795164933","end":140477626,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140477626,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795164986","clinical_significance":[],"strand":1,"feature_type":"variation","end":140477632,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477632,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795165058","clinical_significance":[],"strand":1,"feature_type":"variation","end":140477635,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477635,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477637,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140477637,"clinical_significance":[],"seq_region_name":"7","id":"rs1795165117"},{"end":140477639,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140477639,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130378677"},{"alleles":["T","C"],"end":140477640,"feature_type":"variation","strand":1,"source":"dbSNP","start":140477640,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795165183"},{"source":"dbSNP","start":140477641,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140477641,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795165246"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795165297","alleles":["A","G"],"end":140477647,"feature_type":"variation","strand":1,"source":"dbSNP","start":140477647,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795165343","clinical_significance":[],"start":140477648,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140477648,"strand":1,"feature_type":"variation"},{"end":140477649,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140477649,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795165399"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477650,"source":"dbSNP","strand":1,"feature_type":"variation","end":140477650,"alleles":["G","C"],"seq_region_name":"7","id":"rs1795165457","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1003076385","alleles":["A","C"],"end":140477655,"feature_type":"variation","strand":1,"source":"dbSNP","start":140477655,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140477658,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477658,"clinical_significance":[],"id":"rs1795165572","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs574535260","source":"dbSNP","start":140477659,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140477659,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1456080220","clinical_significance":[],"alleles":["G","C","T"],"end":140477660,"strand":1,"feature_type":"variation","start":140477660,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795165737","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477661,"feature_type":"variation","strand":1,"end":140477661,"alleles":["T","C"]},{"clinical_significance":[],"id":"rs1795165797","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140477662,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477662},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477663,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140477663,"seq_region_name":"7","id":"rs1795165860","clinical_significance":[]},{"source":"dbSNP","start":140477664,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140477664,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795165901"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140477667,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477667,"source":"dbSNP","seq_region_name":"7","id":"rs1795165965","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795166024","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140477669,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477669},{"seq_region_name":"7","id":"rs1795166079","clinical_significance":[],"end":140477670,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140477670,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs958537852","seq_region_name":"7","source":"dbSNP","start":140477672,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140477672,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1211058195","clinical_significance":[],"alleles":["G","A"],"end":140477673,"strand":1,"feature_type":"variation","start":140477673,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477675,"feature_type":"variation","strand":1,"end":140477675,"alleles":["C","G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs973877155"},{"seq_region_name":"7","id":"rs2130378913","clinical_significance":[],"alleles":["C","G"],"end":140477677,"strand":1,"feature_type":"variation","start":140477677,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477678,"feature_type":"variation","strand":1,"end":140477678,"alleles":["G","C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs994473039"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1466722189","end":140477681,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140477681,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["T","A"],"end":140477682,"strand":1,"feature_type":"variation","start":140477682,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795166469","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585503537","clinical_significance":[],"strand":1,"feature_type":"variation","end":140477684,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477684,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477684,"feature_type":"variation","strand":1,"alleles":["CTT","-"],"end":140477686,"clinical_significance":[],"seq_region_name":"7","id":"rs61034923"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477684,"feature_type":"variation","strand":1,"alleles":["CTT","CTTCTT"],"end":140477686,"clinical_significance":[],"id":"rs769972180","seq_region_name":"7"},{"alleles":["T","G"],"end":140477685,"strand":1,"feature_type":"variation","start":140477685,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs543151817","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795166623","clinical_significance":[],"end":140477686,"alleles":["TT","T"],"strand":1,"feature_type":"variation","start":140477685,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs763980967","clinical_significance":[],"alleles":["TTA","-"],"end":140477687,"strand":1,"feature_type":"variation","start":140477685,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585503576","feature_type":"variation","strand":1,"end":140477686,"alleles":["T","C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477686},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477687,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140477687,"clinical_significance":[],"seq_region_name":"7","id":"rs1372489001"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477689,"source":"dbSNP","strand":1,"feature_type":"variation","end":140477689,"alleles":["C","T"],"id":"rs1369899640","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477694,"source":"dbSNP","strand":1,"feature_type":"variation","end":140477694,"alleles":["G","T"],"seq_region_name":"7","id":"rs1321145321","clinical_significance":[]},{"seq_region_name":"7","id":"rs1458819168","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477695,"source":"dbSNP","strand":1,"feature_type":"variation","end":140477695,"alleles":["C","T"]},{"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140477696,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477696,"clinical_significance":[],"seq_region_name":"7","id":"rs951402797"},{"id":"rs1158534795","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477697,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["ATCCGCCCGCC","-"],"end":140477707},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477699,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140477699,"clinical_significance":[],"seq_region_name":"7","id":"rs1415076018"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795167642","feature_type":"variation","strand":1,"alleles":["CCGCCCGCC","CC"],"end":140477707,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477699},{"clinical_significance":[],"id":"rs1563099313","seq_region_name":"7","end":140477700,"alleles":["C","A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140477700,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140477701,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140477701,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1427559923","seq_region_name":"7","clinical_significance":[]},{"id":"rs1795167851","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477702,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140477702},{"clinical_significance":[],"id":"rs1396494016","seq_region_name":"7","feature_type":"variation","strand":1,"end":140477703,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477703},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140477704,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477704,"clinical_significance":[],"seq_region_name":"7","id":"rs1795167970"},{"strand":1,"feature_type":"variation","end":140477705,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477705,"source":"dbSNP","seq_region_name":"7","id":"rs982699922","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795168099","alleles":["C","T"],"end":140477707,"feature_type":"variation","strand":1,"source":"dbSNP","start":140477707,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1249110854","source":"dbSNP","start":140477708,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140477708,"alleles":["T","A"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140477709,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140477709,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1190895147","seq_region_name":"7"},{"seq_region_name":"7","id":"rs907906081","clinical_significance":[],"strand":1,"feature_type":"variation","end":140477710,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477710,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795168312","clinical_significance":[],"end":140477711,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140477711,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1795168370","seq_region_name":"7","clinical_significance":[],"end":140477712,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140477712,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1746901302","seq_region_name":"7","alleles":["C","A","T"],"end":140477713,"feature_type":"variation","strand":1,"source":"dbSNP","start":140477713,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140477715,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140477715,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs368885258"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1463975959","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477718,"feature_type":"variation","strand":1,"end":140477718,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs1338421980","clinical_significance":[],"end":140477773,"alleles":["GCTGGGATTACAGGCGTGAGCCACCACGCCGACCTAGCCACCCCGACAGGC","GC"],"strand":1,"feature_type":"variation","start":140477723,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1214497016","seq_region_name":"7","source":"dbSNP","start":140477725,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140477725,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477728,"feature_type":"variation","strand":1,"end":140477728,"alleles":["G","A"],"clinical_significance":[],"id":"rs944715523","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1312212379","alleles":["A","-"],"end":140477729,"feature_type":"variation","strand":1,"source":"dbSNP","start":140477729,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs561232195","source":"dbSNP","start":140477733,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140477733,"alleles":["C","T"],"feature_type":"variation","strand":1},{"start":140477735,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140477735,"alleles":["G","C"],"strand":1,"feature_type":"variation","id":"rs1231689108","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795168900","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477736,"feature_type":"variation","strand":1,"end":140477736,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1795168971","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477737,"source":"dbSNP","strand":1,"feature_type":"variation","end":140477737,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1795169037","clinical_significance":[],"start":140477738,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140477738,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140477740,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477740,"clinical_significance":[],"id":"rs1280313160","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477742,"feature_type":"variation","strand":1,"end":140477742,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1272776266"},{"end":140477753,"alleles":["GCCACCACGCCG","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140477742,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1563099338","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1318763409","seq_region_name":"7","alleles":["C","T"],"end":140477743,"feature_type":"variation","strand":1,"source":"dbSNP","start":140477743,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1795169332","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477746,"feature_type":"variation","strand":1,"end":140477746,"alleles":["C","T"]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140477749,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477749,"source":"dbSNP","id":"rs1200577279","seq_region_name":"7","clinical_significance":[]},{"start":140477749,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140477751,"alleles":["CGC","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795169434","clinical_significance":[]},{"seq_region_name":"7","id":"rs1250165035","clinical_significance":[],"end":140477753,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140477753,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140477755,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477755,"clinical_significance":[],"seq_region_name":"7","id":"rs1436978359"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477756,"feature_type":"variation","strand":1,"end":140477756,"alleles":["C","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795169667"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1040443737","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477757,"feature_type":"variation","strand":1,"end":140477757,"alleles":["T","C"]},{"source":"dbSNP","start":140477759,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140477767,"alleles":["GCCACCCCG","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795169808"},{"alleles":["C","T"],"end":140477760,"strand":1,"feature_type":"variation","start":140477760,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1781370326","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477763,"feature_type":"variation","strand":1,"end":140477763,"alleles":["C","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs921980199"},{"source":"dbSNP","start":140477764,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140477764,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795169943"},{"id":"rs1795170034","seq_region_name":"7","clinical_significance":[],"end":140477769,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140477769,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477771,"feature_type":"variation","strand":1,"end":140477771,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795170098"},{"start":140477774,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140477774,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1258711491","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140477775,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477775,"source":"dbSNP","seq_region_name":"7","id":"rs1795170255","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477776,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140477776,"clinical_significance":[],"seq_region_name":"7","id":"rs1563099351"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1474430228","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140477777,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477777},{"end":140477779,"alleles":["TTT","TTTT"],"strand":1,"feature_type":"variation","start":140477777,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1563099354","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477779,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140477779,"id":"rs1360904873","seq_region_name":"7","clinical_significance":[]},{"end":140477780,"alleles":["C","A","G"],"strand":1,"feature_type":"variation","start":140477780,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1186854599","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1423871552","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140477781,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477781},{"seq_region_name":"7","id":"rs1174043104","clinical_significance":[],"alleles":["C","A","T"],"end":140477784,"strand":1,"feature_type":"variation","start":140477784,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795170739","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477789,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AAAA","AAA"],"end":140477792},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795170795","source":"dbSNP","start":140477790,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140477790,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs374789407","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477794,"feature_type":"variation","strand":1,"alleles":["A","-"],"end":140477794},{"seq_region_name":"7","id":"rs1019104855","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477794,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","T"],"end":140477794},{"id":"rs1795170991","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477795,"source":"dbSNP","strand":1,"feature_type":"variation","end":140477795,"alleles":["T","C"]},{"alleles":["T","C"],"end":140477797,"strand":1,"feature_type":"variation","start":140477797,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1478539689","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795171120","clinical_significance":[],"strand":1,"feature_type":"variation","end":140477797,"alleles":["T","TT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477797,"source":"dbSNP"},{"source":"dbSNP","start":140477798,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140477798,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1390999159"},{"seq_region_name":"7","id":"rs761942491","clinical_significance":[],"end":140477802,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140477802,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1795171308","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477803,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140477803},{"start":140477804,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140477804,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795171367","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795171429","end":140477805,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140477805,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795171495","alleles":["T","C"],"end":140477808,"feature_type":"variation","strand":1,"source":"dbSNP","start":140477808,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1353364015","clinical_significance":[],"start":140477810,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140477810,"alleles":["T","C","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1054524444","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140477811,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477811,"source":"dbSNP"},{"end":140477812,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140477812,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1419454598"},{"clinical_significance":[],"id":"rs1182892830","seq_region_name":"7","source":"dbSNP","start":140477815,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140477815,"alleles":["C","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795171783","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140477818,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477818,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140477819,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477819,"clinical_significance":[],"seq_region_name":"7","id":"rs1483294564"},{"source":"dbSNP","start":140477821,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140477821,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795171874"},{"seq_region_name":"7","id":"rs1466501156","clinical_significance":[],"end":140477823,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140477823,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1304447496","clinical_significance":[],"end":140477824,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140477824,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477826,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140477826,"clinical_significance":[],"id":"rs528523311","seq_region_name":"7"},{"seq_region_name":"7","id":"rs964616838","clinical_significance":[],"start":140477833,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140477833,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"end":140477836,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140477836,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1230372945"},{"seq_region_name":"7","id":"rs2130379897","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477841,"source":"dbSNP","strand":1,"feature_type":"variation","end":140477843,"alleles":["AGA","A"]},{"clinical_significance":[],"id":"rs1697868728","seq_region_name":"7","alleles":["A","G"],"end":140477845,"feature_type":"variation","strand":1,"source":"dbSNP","start":140477845,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1292956488","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477846,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140477846},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140477848,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477848,"source":"dbSNP","seq_region_name":"7","id":"rs540906635","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140477851,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477851,"source":"dbSNP","seq_region_name":"7","id":"rs974944077","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1294783741","feature_type":"variation","strand":1,"end":140477855,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477855},{"end":140477856,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140477856,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1341322862","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585503900","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140477857,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477857},{"strand":1,"feature_type":"variation","alleles":["G","C","T"],"end":140477858,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477858,"source":"dbSNP","seq_region_name":"7","id":"rs1381242403","clinical_significance":[]},{"source":"dbSNP","start":140477859,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140477859,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1311194308"},{"seq_region_name":"7","id":"rs1414216253","clinical_significance":[],"start":140477861,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140477861,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140477863,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477863,"clinical_significance":[],"seq_region_name":"7","id":"rs893293091"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477864,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140477864,"clinical_significance":[],"id":"rs1220648116","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs773189640","end":140477865,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140477865,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["G","A"],"end":140477867,"strand":1,"feature_type":"variation","start":140477867,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1372801644","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477870,"source":"dbSNP","strand":1,"feature_type":"variation","end":140477870,"alleles":["G","T"],"seq_region_name":"7","id":"rs1306926858","clinical_significance":[]},{"source":"dbSNP","start":140477880,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140477884,"alleles":["AATCA","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795173040"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1426135571","source":"dbSNP","start":140477882,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140477882,"feature_type":"variation","strand":1},{"start":140477886,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140477886,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1010929764","clinical_significance":[]},{"clinical_significance":[],"id":"rs759509572","seq_region_name":"7","end":140477891,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140477891,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1563099442","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477900,"source":"dbSNP","strand":1,"feature_type":"variation","end":140477900,"alleles":["T","C"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477902,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140477902,"seq_region_name":"7","id":"rs1795173356","clinical_significance":[]},{"seq_region_name":"7","id":"rs1234692332","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140477903,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477903,"source":"dbSNP"},{"alleles":["T","C"],"end":140477909,"feature_type":"variation","strand":1,"source":"dbSNP","start":140477909,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs906899009"},{"clinical_significance":[],"seq_region_name":"7","id":"rs867091130","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140477910,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477910},{"seq_region_name":"7","id":"rs565481370","clinical_significance":[],"end":140477911,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140477911,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795173703","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477912,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140477912},{"id":"rs764769419","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140477916,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477916,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795173814","clinical_significance":[],"start":140477918,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140477918,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"start":140477923,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140477923,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs946588651","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477925,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140477925,"id":"rs1795173903","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs372944909","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140477928,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477928},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140477929,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477929,"source":"dbSNP","seq_region_name":"7","id":"rs1002511126","clinical_significance":[]},{"id":"rs1264298896","seq_region_name":"7","clinical_significance":[],"start":140477931,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140477931,"strand":1,"feature_type":"variation"},{"start":140477932,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140477932,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs978107053","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1489079480","alleles":["G","A"],"end":140477934,"feature_type":"variation","strand":1,"source":"dbSNP","start":140477934,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140477938,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477938,"source":"dbSNP","seq_region_name":"7","id":"rs532738433","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795174472","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477944,"feature_type":"variation","strand":1,"alleles":["AT","-"],"end":140477945},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140477945,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477945,"clinical_significance":[],"id":"rs1206783309","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477947,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140477947,"id":"rs1795174595","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477948,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140477948,"clinical_significance":[],"seq_region_name":"7","id":"rs2130380330"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795174648","source":"dbSNP","start":140477949,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140477949,"alleles":["G","C","T"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140477953,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477953,"clinical_significance":[],"seq_region_name":"7","id":"rs550850645"},{"alleles":["T","C"],"end":140477954,"strand":1,"feature_type":"variation","start":140477954,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1184344841","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795174842","seq_region_name":"7","feature_type":"variation","strand":1,"end":140477955,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477955},{"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140477956,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477956,"source":"dbSNP","seq_region_name":"7","id":"rs375876759","clinical_significance":[]},{"seq_region_name":"7","id":"rs7795146","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140477959,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477959,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs188483435","source":"dbSNP","start":140477962,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140477962,"alleles":["A","G"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477963,"source":"dbSNP","strand":1,"feature_type":"variation","end":140477963,"alleles":["C","T"],"seq_region_name":"7","id":"rs1585504114","clinical_significance":[]},{"clinical_significance":[],"id":"rs995239788","seq_region_name":"7","alleles":["T","A"],"end":140477965,"feature_type":"variation","strand":1,"source":"dbSNP","start":140477965,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140477967,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140477967,"clinical_significance":[],"id":"rs1291322601","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795175428","clinical_significance":[],"start":140477969,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140477969,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140477973,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A","C"],"end":140477973,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs528822483"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140477974,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477974,"source":"dbSNP","seq_region_name":"7","id":"rs1795175663","clinical_significance":[]},{"alleles":["A","G"],"end":140477976,"strand":1,"feature_type":"variation","start":140477976,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795175747","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs143421592","source":"dbSNP","start":140477987,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140477987,"alleles":["G","A","C"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140477989,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477989,"source":"dbSNP","seq_region_name":"7","id":"rs1290451348","clinical_significance":[]},{"source":"dbSNP","start":140477992,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140477992,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795175974"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140477993,"source":"dbSNP","strand":1,"feature_type":"variation","end":140477993,"alleles":["C","T"],"seq_region_name":"7","id":"rs1795176036","clinical_significance":[]},{"source":"dbSNP","start":140478004,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C","G"],"end":140478004,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795176093"},{"clinical_significance":[],"seq_region_name":"7","id":"rs868466436","end":140478009,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140478009,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1393166791","seq_region_name":"7","source":"dbSNP","start":140478011,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140478011,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140478013,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478013,"source":"dbSNP","id":"rs1433907540","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1389956185","clinical_significance":[],"alleles":["A","C","G"],"end":140478014,"strand":1,"feature_type":"variation","start":140478014,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140478015,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","TT"],"end":140478015,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130380589","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1396022166","source":"dbSNP","start":140478017,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140478017,"feature_type":"variation","strand":1},{"start":140478022,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C"],"end":140478022,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1298610459","clinical_significance":[]},{"source":"dbSNP","start":140478023,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140478023,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795176515","seq_region_name":"7"},{"alleles":["G","A"],"end":140478026,"feature_type":"variation","strand":1,"source":"dbSNP","start":140478026,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs755960935"},{"seq_region_name":"7","id":"rs117046038","clinical_significance":[],"strand":1,"feature_type":"variation","end":140478028,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478028,"source":"dbSNP"},{"end":140478031,"alleles":["GA","GAGGA"],"strand":1,"feature_type":"variation","start":140478030,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1392956405","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478031,"feature_type":"variation","strand":1,"end":140478031,"alleles":["A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1164769043"},{"strand":1,"feature_type":"variation","end":140478041,"alleles":["CCTTCGAAGG","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478032,"source":"dbSNP","seq_region_name":"7","id":"rs1460476217","clinical_significance":[]},{"end":140478033,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140478033,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795176769"},{"seq_region_name":"7","id":"rs1411969121","clinical_significance":[],"strand":1,"feature_type":"variation","end":140478037,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478037,"source":"dbSNP"},{"alleles":["G","A"],"end":140478040,"strand":1,"feature_type":"variation","start":140478040,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795176898","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1585504227","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478041,"feature_type":"variation","strand":1,"end":140478041,"alleles":["G","C"]},{"seq_region_name":"7","id":"rs1183703388","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478043,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140478043},{"end":140478044,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140478044,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1416991768","seq_region_name":"7"},{"end":140478048,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140478048,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs983138594"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1191593008","feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140478055,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478055},{"seq_region_name":"7","id":"rs1249349673","clinical_significance":[],"strand":1,"feature_type":"variation","end":140478057,"alleles":["TGT","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478055,"source":"dbSNP"},{"alleles":["G","A"],"end":140478056,"feature_type":"variation","strand":1,"source":"dbSNP","start":140478056,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795177338","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1489312404","clinical_significance":[],"alleles":["T","C"],"end":140478057,"strand":1,"feature_type":"variation","start":140478057,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs763862344","clinical_significance":[],"strand":1,"feature_type":"variation","end":140478060,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478060,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1212920700","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478062,"source":"dbSNP","strand":1,"feature_type":"variation","end":140478062,"alleles":["C","A"]},{"feature_type":"variation","strand":1,"end":140478064,"alleles":["T","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478064,"clinical_significance":[],"seq_region_name":"7","id":"rs948253158"},{"alleles":["C","T"],"end":140478065,"feature_type":"variation","strand":1,"source":"dbSNP","start":140478065,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1236942784"},{"seq_region_name":"7","id":"rs1335439380","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478066,"source":"dbSNP","strand":1,"feature_type":"variation","end":140478068,"alleles":["AAA","AA"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478067,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140478067,"clinical_significance":[],"seq_region_name":"7","id":"rs766582118"},{"source":"dbSNP","start":140478071,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140478071,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795177866"},{"clinical_significance":[],"id":"rs1038913347","seq_region_name":"7","source":"dbSNP","start":140478072,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","-"],"end":140478072,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs898765238","alleles":["G","A"],"end":140478073,"feature_type":"variation","strand":1,"source":"dbSNP","start":140478073,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478074,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140478074,"clinical_significance":[],"seq_region_name":"7","id":"rs1369157190"},{"seq_region_name":"7","id":"rs1325826191","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478076,"source":"dbSNP","strand":1,"feature_type":"variation","end":140478076,"alleles":["A","C"]},{"seq_region_name":"7","id":"rs534353721","clinical_significance":[],"end":140478078,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140478078,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795178215","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478079,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140478079},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130380950","end":140478080,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140478080,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140478085,"alleles":["A","C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478085,"clinical_significance":[],"id":"rs1795178266","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1458287358","source":"dbSNP","start":140478086,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140478086,"alleles":["A","G"],"feature_type":"variation","strand":1},{"end":140478087,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140478087,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1391446262","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795178448","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140478089,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478089,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795178511","end":140478097,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140478097,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1287331008","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478098,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140478098},{"seq_region_name":"7","id":"rs1159838960","clinical_significance":[],"alleles":["TACTAC","TAC"],"end":140478104,"strand":1,"feature_type":"variation","start":140478099,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1450951137","end":140478100,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140478100,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs966442619","seq_region_name":"7","clinical_significance":[],"start":140478115,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140478115,"strand":1,"feature_type":"variation"},{"start":140478120,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140478120,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1325314312","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1176262995","feature_type":"variation","strand":1,"alleles":["A","-"],"end":140478123,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478123},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140478123,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478123,"clinical_significance":[],"seq_region_name":"7","id":"rs1434692346"},{"end":140478124,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140478124,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1250981199","clinical_significance":[]},{"seq_region_name":"7","id":"rs994400729","clinical_significance":[],"start":140478125,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140478125,"alleles":["T","G"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140478132,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478132,"clinical_significance":[],"id":"rs1025837372","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1361436204","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","A"],"end":140478135,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478135},{"end":140478136,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140478136,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795179173","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478137,"source":"dbSNP","strand":1,"feature_type":"variation","end":140478137,"alleles":["G","A"],"id":"rs1795179231","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1219866499","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478138,"feature_type":"variation","strand":1,"end":140478138,"alleles":["C","G","T"]},{"id":"rs1249780616","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140478140,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478140,"source":"dbSNP"},{"source":"dbSNP","start":140478144,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C","G"],"end":140478144,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585504423"},{"source":"dbSNP","start":140478148,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140478148,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795179482"},{"end":140478150,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140478150,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs976032552","clinical_significance":[]},{"alleles":["CA","CACA"],"end":140478157,"strand":1,"feature_type":"variation","start":140478156,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795179601","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140478159,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478159,"source":"dbSNP","seq_region_name":"7","id":"rs1795179665","clinical_significance":[]},{"alleles":["C","T"],"end":140478167,"feature_type":"variation","strand":1,"source":"dbSNP","start":140478167,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795179729"},{"alleles":["G","A"],"end":140478168,"feature_type":"variation","strand":1,"source":"dbSNP","start":140478168,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs922033914"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140478169,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478169,"source":"dbSNP","seq_region_name":"7","id":"rs1256822415","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795179895","clinical_significance":[],"end":140478170,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140478170,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["A","G"],"end":140478171,"strand":1,"feature_type":"variation","start":140478171,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795179941","clinical_significance":[]},{"clinical_significance":[],"id":"rs1234139932","seq_region_name":"7","source":"dbSNP","start":140478172,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140478172,"alleles":["T","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795180071","clinical_significance":[],"strand":1,"feature_type":"variation","end":140478177,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478177,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs6962593","source":"dbSNP","start":140478178,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140478178,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs990176652","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478182,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140478182},{"id":"rs1795180282","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140478192,"strand":1,"feature_type":"variation","start":140478192,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1795180349","seq_region_name":"7","end":140478193,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140478193,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1008517231","clinical_significance":[],"start":140478194,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140478194,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1356214732","clinical_significance":[],"start":140478195,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140478195,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478196,"source":"dbSNP","strand":1,"feature_type":"variation","end":140478196,"alleles":["A","G"],"seq_region_name":"7","id":"rs1795180550","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130381356","source":"dbSNP","start":140478197,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140478197,"alleles":["G","C"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478198,"source":"dbSNP","strand":1,"feature_type":"variation","end":140478198,"alleles":["A","G"],"id":"rs1303197795","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478199,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140478199,"seq_region_name":"7","id":"rs1213292739","clinical_significance":[]},{"seq_region_name":"7","id":"rs1018700814","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478203,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140478203},{"seq_region_name":"7","id":"rs1316797247","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478208,"source":"dbSNP","strand":1,"feature_type":"variation","end":140478208,"alleles":["G","A"]},{"start":140478209,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140478209,"alleles":["C","A","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs369936202","clinical_significance":[]},{"start":140478212,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140478212,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1488547601","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140478214,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478214,"source":"dbSNP","seq_region_name":"7","id":"rs996038804","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585504512","source":"dbSNP","start":140478217,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140478217,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140478218,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478218,"clinical_significance":[],"seq_region_name":"7","id":"rs1795181040"},{"alleles":["C","A"],"end":140478219,"strand":1,"feature_type":"variation","start":140478219,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795181099","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1192395993","source":"dbSNP","start":140478224,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140478224,"alleles":["G","A"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478229,"source":"dbSNP","strand":1,"feature_type":"variation","end":140478229,"alleles":["C","T"],"seq_region_name":"7","id":"rs1022526190","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs914766514","end":140478231,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140478231,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795181336","clinical_significance":[],"end":140478238,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140478238,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs571497090","source":"dbSNP","start":140478239,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140478239,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1250550338","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478240,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140478240},{"source":"dbSNP","start":140478241,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140478241,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1453743989"},{"seq_region_name":"7","id":"rs1042371487","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478242,"source":"dbSNP","strand":1,"feature_type":"variation","end":140478242,"alleles":["G","A"]},{"clinical_significance":[],"id":"rs1374744631","seq_region_name":"7","end":140478243,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140478243,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140478248,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140478248,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1190859564","clinical_significance":[]},{"seq_region_name":"7","id":"rs756876163","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478249,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140478249},{"alleles":["AAAAAA","AA","AAAAA","AAAAAAA"],"end":140478254,"feature_type":"variation","strand":1,"source":"dbSNP","start":140478249,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs573514808"},{"strand":1,"feature_type":"variation","end":140478254,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478254,"source":"dbSNP","id":"rs1382018243","seq_region_name":"7","clinical_significance":[]},{"start":140478255,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140478255,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs907414517","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795182054","clinical_significance":[],"end":140478256,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140478256,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140478257,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140478257,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795182110"},{"seq_region_name":"7","id":"rs192175713","clinical_significance":[],"strand":1,"feature_type":"variation","end":140478259,"alleles":["C","A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478259,"source":"dbSNP"},{"start":140478266,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140478266,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs866260692","clinical_significance":[]},{"id":"rs1795182296","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140478267,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478267,"source":"dbSNP"},{"start":140478268,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140478268,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1229637196","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1344690621","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478269,"feature_type":"variation","strand":1,"end":140478269,"alleles":["C","T"]},{"clinical_significance":[],"id":"rs1268940380","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478272,"feature_type":"variation","strand":1,"alleles":["T","-"],"end":140478272},{"id":"rs1227427913","seq_region_name":"7","clinical_significance":[],"end":140478277,"alleles":["TCTTCT","TCT"],"strand":1,"feature_type":"variation","start":140478272,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1437409838","end":140478274,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140478274,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140478275,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140478275,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795182619"},{"strand":1,"feature_type":"variation","end":140478276,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478276,"source":"dbSNP","id":"rs1795182675","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs557152788","source":"dbSNP","start":140478279,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140478279,"alleles":["C","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795182776","source":"dbSNP","start":140478280,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["GTAG","GTAGTAG"],"end":140478283,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478281,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140478281,"seq_region_name":"7","id":"rs1295384419","clinical_significance":[]},{"start":140478283,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140478283,"strand":1,"feature_type":"variation","id":"rs1341581781","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478284,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140478284,"seq_region_name":"7","id":"rs575526244","clinical_significance":[]},{"id":"rs1795182999","seq_region_name":"7","clinical_significance":[],"start":140478285,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C"],"end":140478285,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs745337067","seq_region_name":"7","alleles":["C","G"],"end":140478286,"feature_type":"variation","strand":1,"source":"dbSNP","start":140478286,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478288,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140478288,"seq_region_name":"7","id":"rs1795183135","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795183187","source":"dbSNP","start":140478289,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140478289,"alleles":["G","C"],"feature_type":"variation","strand":1},{"end":140478291,"alleles":["T","C","G"],"strand":1,"feature_type":"variation","start":140478291,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1416056703","clinical_significance":[]},{"seq_region_name":"7","id":"rs1373270438","clinical_significance":[],"strand":1,"feature_type":"variation","end":140478294,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478294,"source":"dbSNP"},{"seq_region_name":"7","id":"rs916683367","clinical_significance":[],"start":140478299,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140478299,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795183434","source":"dbSNP","start":140478300,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","AA"],"end":140478300,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478303,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140478303,"seq_region_name":"7","id":"rs948109483","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140478311,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478311,"source":"dbSNP","seq_region_name":"7","id":"rs1430181122","clinical_significance":[]},{"seq_region_name":"7","id":"rs894126813","clinical_significance":[],"strand":1,"feature_type":"variation","end":140478314,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478314,"source":"dbSNP"},{"id":"rs1398275303","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478314,"source":"dbSNP","strand":1,"feature_type":"variation","end":140478315,"alleles":["CC","C"]},{"end":140478317,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140478317,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130381905"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478318,"feature_type":"variation","strand":1,"end":140478318,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1165931440"},{"seq_region_name":"7","id":"rs543122788","clinical_significance":[],"alleles":["C","A","G"],"end":140478319,"strand":1,"feature_type":"variation","start":140478319,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs920120686","end":140478323,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140478323,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1379650613","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140478324,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478324,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795183983","feature_type":"variation","strand":1,"end":140478325,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478325},{"clinical_significance":[],"id":"rs1368957864","seq_region_name":"7","feature_type":"variation","strand":1,"end":140478326,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478326},{"end":140478331,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140478331,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1222398732","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795184152","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478338,"source":"dbSNP","strand":1,"feature_type":"variation","end":140478338,"alleles":["T","G"]},{"clinical_significance":[],"id":"rs1026726526","seq_region_name":"7","alleles":["T","C"],"end":140478339,"feature_type":"variation","strand":1,"source":"dbSNP","start":140478339,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs886948780","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478342,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140478342},{"start":140478342,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TAATA","TA"],"end":140478346,"strand":1,"feature_type":"variation","id":"rs930135847","seq_region_name":"7","clinical_significance":[]},{"start":140478343,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AA","A"],"end":140478344,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795184379","clinical_significance":[]},{"start":140478344,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140478344,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1004010400","clinical_significance":[]},{"id":"rs1270736062","seq_region_name":"7","clinical_significance":[],"start":140478345,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140478345,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140478347,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478347,"clinical_significance":[],"id":"rs891342168","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140478348,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478348,"clinical_significance":[],"seq_region_name":"7","id":"rs562391630"},{"alleles":["T","A"],"end":140478349,"strand":1,"feature_type":"variation","start":140478349,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795184679","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478352,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140478352,"seq_region_name":"7","id":"rs757951911","clinical_significance":[]},{"seq_region_name":"7","id":"rs1008526960","clinical_significance":[],"start":140478357,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140478357,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs965295782","feature_type":"variation","strand":1,"end":140478359,"alleles":["A","C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478359},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140478360,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478360,"clinical_significance":[],"id":"rs1286427352","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795184999","feature_type":"variation","strand":1,"alleles":["AAACCAAAACCAAA","AAACCAAAACCAAAACCAAA"],"end":140478377,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478364},{"seq_region_name":"7","id":"rs1795185065","clinical_significance":[],"start":140478372,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140478372,"strand":1,"feature_type":"variation"},{"alleles":["C","T"],"end":140478373,"strand":1,"feature_type":"variation","start":140478373,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs900269151","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140478377,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478377,"source":"dbSNP","seq_region_name":"7","id":"rs1585504861","clinical_significance":[]},{"id":"rs996353845","seq_region_name":"7","clinical_significance":[],"alleles":["CTCTCTCTCT","CTCTCT","CTCTCTCT","CTCTCTCTCTCT"],"end":140478388,"strand":1,"feature_type":"variation","start":140478379,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1239913772","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478380,"source":"dbSNP","strand":1,"feature_type":"variation","end":140478380,"alleles":["T","A","C"]},{"source":"dbSNP","start":140478381,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140478381,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795185425","seq_region_name":"7"},{"end":140478383,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140478383,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs975288394","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1337145232","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478383,"feature_type":"variation","strand":1,"alleles":["C","CC"],"end":140478383},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795185725","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478394,"feature_type":"variation","strand":1,"end":140478394,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1409116844","source":"dbSNP","start":140478396,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140478396,"alleles":["G","A","C"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478398,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140478398,"seq_region_name":"7","id":"rs1563099664","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478399,"source":"dbSNP","strand":1,"feature_type":"variation","end":140478399,"alleles":["A","T"],"id":"rs2130382247","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs967908716","clinical_significance":[],"alleles":["A","G"],"end":140478400,"strand":1,"feature_type":"variation","start":140478400,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478401,"source":"dbSNP","strand":1,"feature_type":"variation","end":140478401,"alleles":["G","A"],"seq_region_name":"7","id":"rs1028974717","clinical_significance":[]},{"seq_region_name":"7","id":"rs1166943209","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478404,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140478404},{"seq_region_name":"7","id":"rs780525860","clinical_significance":[],"end":140478405,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140478405,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140478407,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140478407,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795186208","clinical_significance":[]},{"source":"dbSNP","start":140478407,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TTT","TT"],"end":140478409,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795186267"},{"start":140478414,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["CCC","C","CCCC"],"end":140478416,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1459949789","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1326169273","end":140478416,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140478416,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs953378487","alleles":["T","A"],"end":140478418,"feature_type":"variation","strand":1,"source":"dbSNP","start":140478418,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs990230571","alleles":["C","G"],"end":140478419,"feature_type":"variation","strand":1,"source":"dbSNP","start":140478419,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1219666703","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478420,"source":"dbSNP","strand":1,"feature_type":"variation","end":140478421,"alleles":["GG","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs747577739","end":140478422,"alleles":["A","C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140478422,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795186780","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140478428,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478428,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478432,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140478432,"id":"rs1181576929","seq_region_name":"7","clinical_significance":[]},{"id":"rs1167281909","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478437,"source":"dbSNP","strand":1,"feature_type":"variation","end":140478437,"alleles":["C","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795186908","alleles":["AAAAGA","A"],"end":140478443,"feature_type":"variation","strand":1,"source":"dbSNP","start":140478438,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1452501132","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140478442,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478442},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795187050","source":"dbSNP","start":140478443,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140478443,"feature_type":"variation","strand":1},{"id":"rs371227317","seq_region_name":"7","clinical_significance":[],"start":140478444,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140478444,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140478445,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478445,"clinical_significance":[],"seq_region_name":"7","id":"rs1275611313"},{"seq_region_name":"7","id":"rs1795187239","clinical_significance":[],"start":140478447,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140478447,"strand":1,"feature_type":"variation"},{"start":140478450,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A","C"],"end":140478450,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1392459494","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478454,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140478454,"clinical_significance":[],"seq_region_name":"7","id":"rs1795187385"},{"strand":1,"feature_type":"variation","end":140478458,"alleles":["G","C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478458,"source":"dbSNP","id":"rs946212144","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130382480","source":"dbSNP","start":140478460,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140478460,"alleles":["G","T"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478461,"feature_type":"variation","strand":1,"end":140478461,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795187520"},{"end":140478464,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140478464,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1460972970","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478468,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140478468,"seq_region_name":"7","id":"rs1375123229","clinical_significance":[]},{"clinical_significance":[],"id":"rs1277361442","seq_region_name":"7","alleles":["A","C"],"end":140478470,"feature_type":"variation","strand":1,"source":"dbSNP","start":140478470,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1795187748","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478470,"feature_type":"variation","strand":1,"end":140478471,"alleles":["AA","AAA"]},{"start":140478473,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140478473,"strand":1,"feature_type":"variation","id":"rs555136349","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478476,"source":"dbSNP","strand":1,"feature_type":"variation","end":140478476,"alleles":["C","T"],"seq_region_name":"7","id":"rs1795187889","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478477,"source":"dbSNP","strand":1,"feature_type":"variation","end":140478477,"alleles":["A","G"],"seq_region_name":"7","id":"rs1332686154","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478488,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140478488,"clinical_significance":[],"seq_region_name":"7","id":"rs992190224"},{"start":140478488,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140478509,"alleles":["ACCGCGGGTGGAGAAGACGACC","ACCGCGGGTGGAGAAGACGACCGCGGGTGGAGAAGACGACC"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1338015979","clinical_significance":[]},{"seq_region_name":"7","id":"rs977596051","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140478489,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478489,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs761880647","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478492,"feature_type":"variation","strand":1,"end":140478492,"alleles":["C","-"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795188193","end":140478492,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140478492,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140478493,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478493,"source":"dbSNP","seq_region_name":"7","id":"rs1160053933","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478493,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GGG","GG"],"end":140478495,"seq_region_name":"7","id":"rs1393614647","clinical_significance":[]},{"start":140478496,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140478496,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1402480253","clinical_significance":[]},{"clinical_significance":[],"id":"rs1406089443","seq_region_name":"7","source":"dbSNP","start":140478499,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140478499,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1158153415","seq_region_name":"7","source":"dbSNP","start":140478500,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140478500,"alleles":["G","A","C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs916590713","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140478502,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478502,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140478503,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478503,"source":"dbSNP","seq_region_name":"7","id":"rs1192126939","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478505,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","CACCC"],"end":140478505,"id":"rs1795188877","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","C"],"end":140478507,"strand":1,"feature_type":"variation","start":140478507,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585505117","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs386718466","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478510,"feature_type":"variation","strand":1,"alleles":["CCGGCCCCCGAACGCCTG","GCGGGTGGAGAAGACGACCCCGGCCCCCGAACGCCTC"],"end":140478527},{"seq_region_name":"7","id":"rs928780347","clinical_significance":[],"alleles":["C","A"],"end":140478511,"strand":1,"feature_type":"variation","start":140478511,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140478513,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140478513,"alleles":["G","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585505137","clinical_significance":[]},{"seq_region_name":"7","id":"rs371387410","clinical_significance":[],"end":140478513,"alleles":["-","GTGGAGAAGA"],"strand":1,"feature_type":"variation","start":140478514,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1260477980","source":"dbSNP","start":140478514,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140478514,"alleles":["C","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs969400384","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478516,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140478516},{"feature_type":"variation","strand":1,"end":140478517,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478517,"clinical_significance":[],"seq_region_name":"7","id":"rs1215917477"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795189405","source":"dbSNP","start":140478519,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140478519,"feature_type":"variation","strand":1},{"id":"rs938936757","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140478522,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478522,"source":"dbSNP"},{"end":140478526,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140478526,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1281709587","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478526,"feature_type":"variation","strand":1,"alleles":["TGCTT","T"],"end":140478530,"clinical_significance":[],"seq_region_name":"7","id":"rs1795189558"},{"seq_region_name":"7","id":"rs4431522","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478527,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C","T"],"end":140478527},{"start":140478531,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140478531,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795189766","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795189829","source":"dbSNP","start":140478532,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140478532,"alleles":["T","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs73735283","clinical_significance":[],"start":140478535,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140478535,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1795189974","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140478541,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478541,"source":"dbSNP"},{"source":"dbSNP","start":140478542,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140478542,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795190037"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478544,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140478544,"seq_region_name":"7","id":"rs1305415895","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1333583306","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478546,"feature_type":"variation","strand":1,"end":140478546,"alleles":["G","A","T"]},{"source":"dbSNP","start":140478547,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140478547,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795190244","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140478548,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478548,"clinical_significance":[],"id":"rs1047185471","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795190382","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140478556,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478556,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1585505214","clinical_significance":[],"end":140478558,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140478558,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs912830131","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140478559,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478559,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1259386846","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140478560,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478560},{"start":140478562,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140478562,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795190622","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs930931751","end":140478566,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140478566,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140478567,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140478567,"alleles":["A","G"],"strand":1,"feature_type":"variation","id":"rs1343439091","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563099753","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478568,"feature_type":"variation","strand":1,"end":140478568,"alleles":["T","C"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478569,"feature_type":"variation","strand":1,"end":140478573,"alleles":["ACAAA","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795190843"},{"clinical_significance":[],"id":"rs944265094","seq_region_name":"7","source":"dbSNP","start":140478570,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140478570,"alleles":["C","T"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["AAGAAGAA","AAGAA"],"end":140478579,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478572,"clinical_significance":[],"seq_region_name":"7","id":"rs1436034400"},{"seq_region_name":"7","id":"rs1795191037","clinical_significance":[],"alleles":["G","C","T"],"end":140478574,"strand":1,"feature_type":"variation","start":140478574,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140478575,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140478575,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130383005"},{"seq_region_name":"7","id":"rs367800830","clinical_significance":[],"start":140478577,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C"],"end":140478577,"strand":1,"feature_type":"variation"},{"alleles":["C","A","T"],"end":140478583,"strand":1,"feature_type":"variation","start":140478583,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1172205066","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1039938722","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478584,"feature_type":"variation","strand":1,"end":140478584,"alleles":["A","G"]},{"end":140478588,"alleles":["G","C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140478588,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs886838772"},{"alleles":["G","-"],"end":140478588,"strand":1,"feature_type":"variation","start":140478588,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1237845591","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478589,"feature_type":"variation","strand":1,"end":140478589,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs748350041"},{"id":"rs1795191537","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478589,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CTTCTTCT","CTTCT"],"end":140478596},{"alleles":["T","G"],"end":140478591,"strand":1,"feature_type":"variation","start":140478591,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795191595","clinical_significance":[]},{"end":140478592,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140478592,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1190402344"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478594,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140478594,"seq_region_name":"7","id":"rs1043868651","clinical_significance":[]},{"alleles":["C","T"],"end":140478595,"feature_type":"variation","strand":1,"source":"dbSNP","start":140478595,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795191786"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1019472394","source":"dbSNP","start":140478599,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140478599,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1485818335","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478600,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140478600},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140478601,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478601,"clinical_significance":[],"id":"rs1281975860","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140478602,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478602,"clinical_significance":[],"seq_region_name":"7","id":"rs900996019"},{"seq_region_name":"7","id":"rs996759864","clinical_significance":[],"end":140478606,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140478606,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795192197","clinical_significance":[],"end":140478608,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140478608,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478611,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140478611,"seq_region_name":"7","id":"rs1795192257","clinical_significance":[]},{"id":"rs1028190753","seq_region_name":"7","clinical_significance":[],"alleles":["G","A","T"],"end":140478612,"strand":1,"feature_type":"variation","start":140478612,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795192382","clinical_significance":[],"start":140478614,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140478614,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478615,"feature_type":"variation","strand":1,"end":140478620,"alleles":["GGGGGG","GGGGG"],"clinical_significance":[],"id":"rs1346807458","seq_region_name":"7"},{"alleles":["GGG","GGGACGGAGGG"],"end":140478619,"strand":1,"feature_type":"variation","start":140478617,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1296212661","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs545184733","feature_type":"variation","strand":1,"alleles":["GGGGCGGAGGG","GGG","GGGGCGGAGGGGCGGAGGG"],"end":140478627,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478617},{"clinical_significance":[],"seq_region_name":"7","id":"rs4427086","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478620,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140478620},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478621,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140478621,"id":"rs1408722914","seq_region_name":"7","clinical_significance":[]},{"start":140478621,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["CGGAGGGACGGAGGGACG","CGGAGGGACG","CGGAGGGACGGAGGGACGGAGGGACG"],"end":140478638,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs896300607","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs990130148","alleles":["G","T"],"end":140478622,"feature_type":"variation","strand":1,"source":"dbSNP","start":140478622,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1022148309","seq_region_name":"7","clinical_significance":[],"start":140478623,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140478623,"strand":1,"feature_type":"variation"},{"id":"rs1563099809","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140478624,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478624,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1328769847","clinical_significance":[],"alleles":["G","C"],"end":140478625,"strand":1,"feature_type":"variation","start":140478625,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140478626,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140478626,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1013948310"},{"strand":1,"feature_type":"variation","end":140478627,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478627,"source":"dbSNP","seq_region_name":"7","id":"rs1023541892","clinical_significance":[]},{"source":"dbSNP","start":140478628,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140478628,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795193069"},{"start":140478629,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140478629,"alleles":["C","CC"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795193122","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140478630,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478630,"source":"dbSNP","id":"rs1427311348","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140478634,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140478634,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585505452"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478635,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140478635,"seq_region_name":"7","id":"rs1419387941","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140478638,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478638,"source":"dbSNP","id":"rs967515322","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795193405","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478640,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140478640},{"seq_region_name":"7","id":"rs969832114","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140478642,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478642,"source":"dbSNP"},{"end":140478645,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140478645,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1475222266","clinical_significance":[]},{"source":"dbSNP","start":140478647,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140478647,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795193600","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795193654","end":140478648,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140478648,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1259194764","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478649,"feature_type":"variation","strand":1,"end":140478649,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795193719","source":"dbSNP","start":140478651,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140478651,"alleles":["A","G"],"feature_type":"variation","strand":1},{"alleles":["A","G"],"end":140478653,"feature_type":"variation","strand":1,"source":"dbSNP","start":140478653,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs544522428"},{"clinical_significance":[],"seq_region_name":"7","id":"rs112456354","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478657,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140478657},{"alleles":["G","A"],"end":140478658,"feature_type":"variation","strand":1,"source":"dbSNP","start":140478658,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs73480264","seq_region_name":"7"},{"source":"dbSNP","start":140478660,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140478660,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795193931"},{"strand":1,"feature_type":"variation","end":140478661,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478661,"source":"dbSNP","seq_region_name":"7","id":"rs1310743001","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795194054","feature_type":"variation","strand":1,"end":140478662,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478662},{"clinical_significance":[],"id":"rs1485137928","seq_region_name":"7","end":140478665,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140478665,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140478666,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478666,"source":"dbSNP","id":"rs1251732801","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478667,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140478667,"clinical_significance":[],"seq_region_name":"7","id":"rs977887919"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1206326304","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478667,"feature_type":"variation","strand":1,"end":140478673,"alleles":["GAGAGAG","GAGAG","GAGAGAGAG"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478668,"source":"dbSNP","strand":1,"feature_type":"variation","end":140478668,"alleles":["A","AA"],"seq_region_name":"7","id":"rs1272152108","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140478668,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478668,"clinical_significance":[],"seq_region_name":"7","id":"rs1795194408"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140478669,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478669,"clinical_significance":[],"id":"rs1354461954","seq_region_name":"7"},{"source":"dbSNP","start":140478669,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["GAGAGGAGAGG","GAGAGG"],"end":140478679,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1234000004"},{"start":140478670,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140478670,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2094788678","clinical_significance":[]},{"clinical_significance":[],"id":"rs773525976","seq_region_name":"7","alleles":["G","T"],"end":140478671,"feature_type":"variation","strand":1,"source":"dbSNP","start":140478671,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478673,"source":"dbSNP","strand":1,"feature_type":"variation","end":140478673,"alleles":["G","C"],"id":"rs960185356","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795194783","clinical_significance":[],"start":140478674,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140478674,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478676,"source":"dbSNP","strand":1,"feature_type":"variation","end":140478676,"alleles":["G","A"],"id":"rs1218810711","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478677,"source":"dbSNP","strand":1,"feature_type":"variation","end":140478677,"alleles":["A","T"],"seq_region_name":"7","id":"rs991747357","clinical_significance":[]},{"end":140478678,"alleles":["G","C","T"],"strand":1,"feature_type":"variation","start":140478678,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs763107303","clinical_significance":[]},{"clinical_significance":[],"id":"rs1166031615","seq_region_name":"7","end":140478679,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140478679,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478683,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140478683,"seq_region_name":"7","id":"rs1461510791","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs982933619","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478685,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140478685},{"strand":1,"feature_type":"variation","end":140478686,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478686,"source":"dbSNP","seq_region_name":"7","id":"rs1795195263","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795195314","source":"dbSNP","start":140478687,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140478687,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs375326503","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478688,"feature_type":"variation","strand":1,"end":140478688,"alleles":["C","G"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478691,"source":"dbSNP","strand":1,"feature_type":"variation","end":140478691,"alleles":["G","A"],"seq_region_name":"7","id":"rs1185137084","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs912754485","source":"dbSNP","start":140478692,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140478692,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478693,"source":"dbSNP","strand":1,"feature_type":"variation","end":140478693,"alleles":["C","T"],"seq_region_name":"7","id":"rs1585505575","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130383729","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478699,"source":"dbSNP","strand":1,"feature_type":"variation","end":140478699,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs944207796","end":140478702,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140478702,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1279558458","alleles":["G","A"],"end":140478703,"feature_type":"variation","strand":1,"source":"dbSNP","start":140478703,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1479506675","source":"dbSNP","start":140478704,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140478704,"feature_type":"variation","strand":1},{"start":140478705,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140478705,"strand":1,"feature_type":"variation","id":"rs916126313","seq_region_name":"7","clinical_significance":[]},{"id":"rs976105354","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478706,"source":"dbSNP","strand":1,"feature_type":"variation","end":140478706,"alleles":["G","C","T"]},{"start":140478712,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140478712,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795195921","clinical_significance":[]},{"start":140478713,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140478713,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795195982","clinical_significance":[]},{"end":140478715,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140478715,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1336804294","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795196110","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478716,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140478716},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478717,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140478717,"clinical_significance":[],"seq_region_name":"7","id":"rs930984914"},{"alleles":["G","A","T"],"end":140478718,"strand":1,"feature_type":"variation","start":140478718,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs921523466","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs908258724","end":140478719,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140478719,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478720,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140478720,"seq_region_name":"7","id":"rs1309364934","clinical_significance":[]},{"source":"dbSNP","start":140478721,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140478721,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795196402"},{"strand":1,"feature_type":"variation","end":140478724,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478724,"source":"dbSNP","seq_region_name":"7","id":"rs1585505645","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1048030201","feature_type":"variation","strand":1,"end":140478725,"alleles":["G","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478725},{"feature_type":"variation","strand":1,"end":140478727,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478727,"clinical_significance":[],"id":"rs908190772","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478729,"feature_type":"variation","strand":1,"end":140478729,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs939810162"},{"end":140478730,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140478730,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1443824980","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478731,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140478731,"id":"rs1208423046","seq_region_name":"7","clinical_significance":[]},{"id":"rs1795196853","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140478732,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478732,"source":"dbSNP"},{"alleles":["G","A"],"end":140478733,"strand":1,"feature_type":"variation","start":140478733,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795196917","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478735,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140478735,"clinical_significance":[],"seq_region_name":"7","id":"rs1795196977"},{"id":"rs1795197048","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140478736,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478736,"source":"dbSNP"},{"alleles":["A","G"],"end":140478737,"strand":1,"feature_type":"variation","start":140478737,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1041189883","clinical_significance":[]},{"seq_region_name":"7","id":"rs750281563","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["CGC","C"],"end":140478741,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478739,"source":"dbSNP"},{"end":140478741,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140478741,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795197240","seq_region_name":"7","clinical_significance":[]},{"start":140478743,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140478743,"alleles":["G","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795197304","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140478745,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478745,"clinical_significance":[],"seq_region_name":"7","id":"rs1485478051"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478746,"source":"dbSNP","strand":1,"feature_type":"variation","end":140478746,"alleles":["A","G"],"seq_region_name":"7","id":"rs1456932599","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795197486","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478747,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140478747},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795197551","end":140478749,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140478749,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1795197620","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478750,"feature_type":"variation","strand":1,"end":140478750,"alleles":["C","A"]},{"end":140478754,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140478754,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs111862082","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130384028","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478756,"source":"dbSNP","strand":1,"feature_type":"variation","end":140478756,"alleles":["C","G"]},{"seq_region_name":"7","id":"rs1795197824","clinical_significance":[],"end":140478758,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140478758,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795197880","clinical_significance":[],"alleles":["T","C"],"end":140478760,"strand":1,"feature_type":"variation","start":140478760,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs935091673","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140478761,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478761},{"strand":1,"feature_type":"variation","end":140478762,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478762,"source":"dbSNP","seq_region_name":"7","id":"rs1795197998","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["ACCACC","ACC"],"end":140478767,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478762,"clinical_significance":[],"seq_region_name":"7","id":"rs1160766159"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1374866219","alleles":["C","A"],"end":140478763,"feature_type":"variation","strand":1,"source":"dbSNP","start":140478763,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795198179","source":"dbSNP","start":140478764,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140478764,"alleles":["C","G","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585505727","feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140478765,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478765},{"source":"dbSNP","start":140478766,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140478766,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795198327"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140478772,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478772,"source":"dbSNP","seq_region_name":"7","id":"rs1416938211","clinical_significance":[]},{"clinical_significance":[],"id":"rs1249628647","seq_region_name":"7","source":"dbSNP","start":140478773,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140478773,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1795198503","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478773,"feature_type":"variation","strand":1,"end":140478778,"alleles":["AGCCCC","-"]},{"strand":1,"feature_type":"variation","end":140478774,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478774,"source":"dbSNP","id":"rs1795198561","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140478775,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140478775,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1194007476"},{"source":"dbSNP","start":140478781,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140478781,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1469802358"},{"alleles":["A","C"],"end":140478782,"feature_type":"variation","strand":1,"source":"dbSNP","start":140478782,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795198730"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478783,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140478783,"seq_region_name":"7","id":"rs1795198781","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795198839","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478785,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140478785},{"id":"rs1795198902","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478786,"source":"dbSNP","strand":1,"feature_type":"variation","end":140478786,"alleles":["G","A"]},{"end":140478787,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140478787,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs2130384193","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140478793,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478793,"clinical_significance":[],"seq_region_name":"7","id":"rs1585505755"},{"id":"rs1251020953","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140478794,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478794,"source":"dbSNP"},{"seq_region_name":"7","id":"rs996602867","clinical_significance":[],"strand":1,"feature_type":"variation","end":140478796,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478796,"source":"dbSNP"},{"alleles":["C","G","T"],"end":140478797,"strand":1,"feature_type":"variation","start":140478797,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1486203754","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140478798,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478798,"clinical_significance":[],"seq_region_name":"7","id":"rs1167898564"},{"alleles":["G","A","T"],"end":140478799,"strand":1,"feature_type":"variation","start":140478799,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs147984240","clinical_significance":[]},{"source":"dbSNP","start":140478800,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140478800,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs548650732"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1012007775","source":"dbSNP","start":140478801,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140478801,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140478802,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478802,"clinical_significance":[],"seq_region_name":"7","id":"rs1311466346"},{"id":"rs1375159497","seq_region_name":"7","clinical_significance":[],"end":140478803,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140478803,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1021648595","clinical_significance":[],"end":140478804,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140478804,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795199721","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478805,"feature_type":"variation","strand":1,"end":140478805,"alleles":["T","A"]},{"end":140478806,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140478806,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1023978194","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1325761303","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140478807,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478807},{"clinical_significance":[],"seq_region_name":"7","id":"rs1385745195","alleles":["C","G"],"end":140478810,"feature_type":"variation","strand":1,"source":"dbSNP","start":140478810,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478811,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140478811,"clinical_significance":[],"id":"rs1795199922","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140478812,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478812,"clinical_significance":[],"seq_region_name":"7","id":"rs2130384350"},{"seq_region_name":"7","id":"rs967777608","clinical_significance":[],"end":140478813,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140478813,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478815,"source":"dbSNP","strand":1,"feature_type":"variation","end":140478815,"alleles":["G","A","T"],"seq_region_name":"7","id":"rs141677563","clinical_significance":[]},{"seq_region_name":"7","id":"rs1747939118","clinical_significance":[],"alleles":["G","T"],"end":140478816,"strand":1,"feature_type":"variation","start":140478816,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1795200090","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478820,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GGGAGG","GGGAGGGAGG"],"end":140478825},{"clinical_significance":[],"id":"rs1035742480","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140478821,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478821},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140478822,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478822,"source":"dbSNP","seq_region_name":"7","id":"rs1795200206","clinical_significance":[]},{"source":"dbSNP","start":140478823,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140478823,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs972175335"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795200324","alleles":["G","A"],"end":140478824,"feature_type":"variation","strand":1,"source":"dbSNP","start":140478824,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795200382","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140478826,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478826,"source":"dbSNP"},{"id":"rs1379272957","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478826,"source":"dbSNP","strand":1,"feature_type":"variation","end":140478862,"alleles":["AGCCAGCCCACCTCTCCCCGATGCGCTCGCAGCCAGC","AGCCAGC"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478827,"feature_type":"variation","strand":1,"end":140478827,"alleles":["G","A","T"],"clinical_significance":[],"id":"rs1795200520","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478828,"source":"dbSNP","strand":1,"feature_type":"variation","end":140478828,"alleles":["C","G"],"seq_region_name":"7","id":"rs1174066932","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795200652","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478832,"source":"dbSNP","strand":1,"feature_type":"variation","end":140478832,"alleles":["C","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478833,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140478833,"clinical_significance":[],"seq_region_name":"7","id":"rs960196712"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478836,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140478836,"clinical_significance":[],"seq_region_name":"7","id":"rs1455385363"},{"alleles":["C","G"],"end":140478837,"feature_type":"variation","strand":1,"source":"dbSNP","start":140478837,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795200835"},{"end":140478842,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140478842,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1393212860","clinical_significance":[]},{"start":140478843,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140478843,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1275406364","clinical_significance":[]},{"clinical_significance":[],"id":"rs991631350","seq_region_name":"7","feature_type":"variation","strand":1,"end":140478844,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478844},{"start":140478847,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140478847,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1264015580","clinical_significance":[]},{"end":140478857,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140478857,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1231924808","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140478858,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478858,"clinical_significance":[],"seq_region_name":"7","id":"rs916178745"},{"id":"rs1795201260","seq_region_name":"7","clinical_significance":[],"start":140478861,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140478861,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1203441033","alleles":["C","T"],"end":140478862,"feature_type":"variation","strand":1,"source":"dbSNP","start":140478862,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1795201470","seq_region_name":"7","end":140478864,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140478864,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140478866,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140478866,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1485685939"},{"seq_region_name":"7","id":"rs1795201638","clinical_significance":[],"strand":1,"feature_type":"variation","end":140478867,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478867,"source":"dbSNP"},{"start":140478868,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140478868,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1279355268","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795201726","clinical_significance":[],"alleles":["A","C","G"],"end":140478869,"strand":1,"feature_type":"variation","start":140478869,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478871,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140478871,"clinical_significance":[],"seq_region_name":"7","id":"rs952968887"},{"seq_region_name":"7","id":"rs995929185","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478872,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140478872},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478873,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140478873,"clinical_significance":[],"id":"rs1795202015","seq_region_name":"7"},{"clinical_significance":[],"id":"rs984761927","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478874,"feature_type":"variation","strand":1,"end":140478874,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1303317020","clinical_significance":[],"end":140478875,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140478875,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140478876,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140478876,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795202267","seq_region_name":"7"},{"end":140478877,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140478877,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs528084379"},{"id":"rs1228867472","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140478879,"alleles":["GGG","GG","GGGG"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478877,"source":"dbSNP"},{"clinical_significance":[],"id":"rs775565034","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478878,"feature_type":"variation","strand":1,"end":140478878,"alleles":["G","A"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478879,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140478879,"seq_region_name":"7","id":"rs1795202652","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","C","G","T"],"end":140478880,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478880,"source":"dbSNP","id":"rs939675232","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","C","G"],"end":140478881,"strand":1,"feature_type":"variation","start":140478881,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1264099918","clinical_significance":[]},{"clinical_significance":[],"id":"rs1445394596","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478882,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140478882},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140478883,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478883,"source":"dbSNP","seq_region_name":"7","id":"rs951365611","clinical_significance":[]},{"seq_region_name":"7","id":"rs1040809206","clinical_significance":[],"alleles":["G","A","C","T"],"end":140478884,"strand":1,"feature_type":"variation","start":140478884,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478886,"source":"dbSNP","strand":1,"feature_type":"variation","end":140478886,"alleles":["A","T"],"seq_region_name":"7","id":"rs1436362079","clinical_significance":[]},{"start":140478888,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140478888,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1247316191","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795203456","clinical_significance":[],"strand":1,"feature_type":"variation","end":140478908,"alleles":["GCGGCGGTGCAGCCCCGCGGC","GCGGCGGTGCAGCCCCGCGGCGCGGCGGTGCAGCCCCGCGGC"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478888,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1455978320","source":"dbSNP","start":140478889,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140478889,"feature_type":"variation","strand":1},{"start":140478894,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140478894,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130384758","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130384769","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478895,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140478895},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478897,"source":"dbSNP","strand":1,"feature_type":"variation","end":140478897,"alleles":["C","T"],"seq_region_name":"7","id":"rs1373466931","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1172247490","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478899,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140478899},{"source":"dbSNP","start":140478900,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140478900,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795203883"},{"seq_region_name":"7","id":"rs1171764694","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478900,"source":"dbSNP","strand":1,"feature_type":"variation","end":140478903,"alleles":["CCCC","CCC"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795204081","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478902,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140478902},{"end":140478903,"alleles":["C","A","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140478903,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs922319016"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130384849","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478905,"feature_type":"variation","strand":1,"end":140478905,"alleles":["C","G"]},{"clinical_significance":[],"id":"rs1795204228","seq_region_name":"7","source":"dbSNP","start":140478906,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140478906,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478907,"feature_type":"variation","strand":1,"end":140478907,"alleles":["G","A"],"clinical_significance":[],"id":"rs1795204285","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795204336","end":140478908,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140478908,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795204385","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478910,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140478910},{"clinical_significance":[],"seq_region_name":"7","id":"rs982858598","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140478915,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478915},{"id":"rs2130384907","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140478916,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478916,"source":"dbSNP"},{"id":"rs2130384929","seq_region_name":"7","clinical_significance":[],"alleles":["A","G"],"end":140478918,"strand":1,"feature_type":"variation","start":140478918,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140478919,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478919,"source":"dbSNP","id":"rs1394927567","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478920,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140478920,"clinical_significance":[],"seq_region_name":"7","id":"rs932507307"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478921,"source":"dbSNP","strand":1,"feature_type":"variation","end":140478921,"alleles":["G","A"],"id":"rs1795204710","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795204765","feature_type":"variation","strand":1,"end":140478923,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478923},{"end":140478926,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140478926,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1477508254","seq_region_name":"7"},{"source":"dbSNP","start":140478926,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["CCGCC","CC"],"end":140478930,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1420677585"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1159987545","alleles":["C","T"],"end":140478927,"feature_type":"variation","strand":1,"source":"dbSNP","start":140478927,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs189350158","clinical_significance":[],"start":140478928,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140478928,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs191111318","alleles":["C","G"],"end":140478929,"feature_type":"variation","strand":1,"source":"dbSNP","start":140478929,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs184547380","seq_region_name":"7","alleles":["C","A"],"end":140478930,"feature_type":"variation","strand":1,"source":"dbSNP","start":140478930,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140478931,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140478931,"strand":1,"feature_type":"variation","id":"rs530420743","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs373373966","source":"dbSNP","start":140478931,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140478932,"alleles":["AG","AGAAG"],"feature_type":"variation","strand":1},{"id":"rs1795205379","seq_region_name":"7","clinical_significance":[],"start":140478932,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140478932,"strand":1,"feature_type":"variation"},{"alleles":["GGCCTCCGCGG","G"],"end":140478942,"strand":1,"feature_type":"variation","start":140478932,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1563100089","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140478932,"alleles":["-","AAA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478933,"clinical_significance":[],"id":"rs1795205484","seq_region_name":"7"},{"start":140478935,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140478963,"alleles":["CTCCGCGGACAGCGCTGAGGGCTCCGCGG","CTCCGCGG"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1342126035","clinical_significance":[]},{"id":"rs1795205599","seq_region_name":"7","clinical_significance":[],"end":140478940,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140478940,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478943,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140478943,"id":"rs947640308","seq_region_name":"7","clinical_significance":[]},{"start":140478944,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["CAGCGCTG","-"],"end":140478951,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1563100102","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140478945,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478945,"source":"dbSNP","seq_region_name":"7","id":"rs1224632774","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795205809","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478946,"source":"dbSNP","strand":1,"feature_type":"variation","end":140478946,"alleles":["G","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs13307121","end":140478947,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140478947,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1563100108","seq_region_name":"7","clinical_significance":[],"start":140478949,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140478949,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478952,"feature_type":"variation","strand":1,"end":140478952,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs893620669"},{"seq_region_name":"7","id":"rs1372463920","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478953,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140478953},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478954,"source":"dbSNP","strand":1,"feature_type":"variation","end":140478954,"alleles":["G","A"],"seq_region_name":"7","id":"rs1795206086","clinical_significance":[]},{"seq_region_name":"7","id":"rs1438626455","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478955,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140478955},{"seq_region_name":"7","id":"rs1010861447","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140478956,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478956,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478957,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140478957,"clinical_significance":[],"id":"rs2130385180","seq_region_name":"7"},{"alleles":["G","A"],"end":140478962,"strand":1,"feature_type":"variation","start":140478962,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1293371796","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["GG","GGG"],"end":140478963,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478962,"source":"dbSNP","id":"rs1795206314","seq_region_name":"7","clinical_significance":[]},{"id":"rs1795206371","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478966,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140478966},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140478969,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478969,"clinical_significance":[],"seq_region_name":"7","id":"rs1416303408"},{"seq_region_name":"7","id":"rs1795206483","clinical_significance":[],"start":140478970,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140478970,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1042688500","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478971,"source":"dbSNP","strand":1,"feature_type":"variation","end":140478971,"alleles":["G","A"]},{"clinical_significance":[],"id":"rs569056791","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140478972,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478972},{"clinical_significance":[],"seq_region_name":"7","id":"rs934974111","feature_type":"variation","strand":1,"end":140478973,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478973},{"seq_region_name":"7","id":"rs999222463","clinical_significance":[],"alleles":["G","C","T"],"end":140478974,"strand":1,"feature_type":"variation","start":140478974,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["GTTG","G"],"end":140478977,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478974,"source":"dbSNP","seq_region_name":"7","id":"rs1398574337","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140478977,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478977,"source":"dbSNP","id":"rs1377432093","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478980,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140478980,"clinical_significance":[],"seq_region_name":"7","id":"rs10257086"},{"seq_region_name":"7","id":"rs1258700749","clinical_significance":[],"strand":1,"feature_type":"variation","end":140478981,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478981,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1474373208","clinical_significance":[],"start":140478984,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140478984,"strand":1,"feature_type":"variation"},{"start":140478987,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140478987,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1237080863","clinical_significance":[]},{"end":140478988,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140478988,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1439866013","seq_region_name":"7","clinical_significance":[]},{"start":140478988,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","TT"],"end":140478988,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795207294","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["GGGGG","GGGGGG"],"end":140478993,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478989,"clinical_significance":[],"id":"rs1348844200","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1585506311","clinical_significance":[],"start":140478990,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140478990,"strand":1,"feature_type":"variation"},{"alleles":["G","A","T"],"end":140478992,"feature_type":"variation","strand":1,"source":"dbSNP","start":140478992,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs960082119"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478993,"feature_type":"variation","strand":1,"end":140478993,"alleles":["G","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1204716622"},{"start":140478996,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140478996,"strand":1,"feature_type":"variation","id":"rs1273894820","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140478998,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140478998,"source":"dbSNP","seq_region_name":"7","id":"rs896196266","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1234552967","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140478999,"feature_type":"variation","strand":1,"end":140478999,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1332259664","clinical_significance":[],"start":140479000,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140479000,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140479001,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140479001,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs949251890","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140479002,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140479002,"source":"dbSNP","seq_region_name":"7","id":"rs1469876276","clinical_significance":[]},{"seq_region_name":"7","id":"rs1044877386","clinical_significance":[],"start":140479007,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140479007,"alleles":["C","A","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795208110","source":"dbSNP","start":140479010,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140479010,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1012992536","feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140479011,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479011},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140479012,"source":"dbSNP","strand":1,"feature_type":"variation","end":140479012,"alleles":["G","A"],"seq_region_name":"7","id":"rs1795208262","clinical_significance":[]},{"alleles":["C","T"],"end":140479013,"feature_type":"variation","strand":1,"source":"dbSNP","start":140479013,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1023163026"},{"alleles":["C","T"],"end":140479014,"strand":1,"feature_type":"variation","start":140479014,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1446014329","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140479015,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140479015,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1395090204"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795208507","source":"dbSNP","start":140479015,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["GCGAGGGCTGC","GC"],"end":140479025,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs905130054","clinical_significance":[],"start":140479019,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C"],"end":140479019,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795208704","feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140479021,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479021},{"seq_region_name":"7","id":"rs995409150","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140479023,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140479023,"source":"dbSNP"},{"alleles":["A","C"],"end":140479026,"strand":1,"feature_type":"variation","start":140479026,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1159301800","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795208969","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140479027,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479027},{"start":140479029,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C"],"end":140479029,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1048287390","clinical_significance":[]},{"id":"rs1227479936","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140479030,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140479030,"source":"dbSNP"},{"end":140479032,"alleles":["C","A","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140479032,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1252894831"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1440739897","source":"dbSNP","start":140479033,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140479033,"feature_type":"variation","strand":1},{"start":140479035,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140479035,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795209478","clinical_significance":[]},{"seq_region_name":"7","id":"rs1184463810","clinical_significance":[],"end":140479037,"alleles":["C","-"],"strand":1,"feature_type":"variation","start":140479037,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1178383382","source":"dbSNP","start":140479038,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C","G"],"end":140479038,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140479041,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140479041,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1362371046"},{"id":"rs1452617923","seq_region_name":"7","clinical_significance":[],"start":140479042,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140479042,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140479043,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140479043,"seq_region_name":"7","id":"rs952991135","clinical_significance":[]},{"source":"dbSNP","start":140479044,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140479044,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1163408991"},{"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140479045,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140479045,"source":"dbSNP","seq_region_name":"7","id":"rs984424923","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795209947","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","-"],"end":140479046,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140479046,"source":"dbSNP"},{"id":"rs887143187","seq_region_name":"7","clinical_significance":[],"start":140479047,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140479047,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1795210052","clinical_significance":[],"start":140479048,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140479048,"alleles":["C","G","T"],"strand":1,"feature_type":"variation"},{"end":140479049,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140479049,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1396117943"},{"start":140479049,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140479053,"alleles":["CCGCC","CC"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795210169","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1016227591","source":"dbSNP","start":140479050,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140479050,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs867986074","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479053,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140479053},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140479058,"source":"dbSNP","strand":1,"feature_type":"variation","end":140479058,"alleles":["C","A"],"seq_region_name":"7","id":"rs1004167944","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs961076035","feature_type":"variation","strand":1,"end":140479059,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479059},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479061,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140479061,"clinical_significance":[],"seq_region_name":"7","id":"rs1795210428"},{"seq_region_name":"7","id":"rs1795210471","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140479065,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140479065,"source":"dbSNP"},{"seq_region_name":"7","id":"rs555099514","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140479069,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140479069},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795210585","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479073,"feature_type":"variation","strand":1,"end":140479073,"alleles":["A","C"]},{"source":"dbSNP","start":140479074,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140479074,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795210637"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795210690","feature_type":"variation","strand":1,"alleles":["GGCCGGCCG","GGCCGGCCGGCCG"],"end":140479082,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479074},{"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140479077,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479077,"clinical_significance":[],"seq_region_name":"7","id":"rs1795210745"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795210812","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479078,"feature_type":"variation","strand":1,"end":140479078,"alleles":["G","A","C"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479079,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140479079,"clinical_significance":[],"seq_region_name":"7","id":"rs1795210876"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130385781","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479080,"feature_type":"variation","strand":1,"end":140479080,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1795210930","clinical_significance":[],"alleles":["C","A","G"],"end":140479081,"strand":1,"feature_type":"variation","start":140479081,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795210989","clinical_significance":[],"strand":1,"feature_type":"variation","end":140479083,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140479083,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1795211030","seq_region_name":"7","source":"dbSNP","start":140479083,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["CCC","CC"],"end":140479085,"feature_type":"variation","strand":1},{"start":140479084,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G","T"],"end":140479084,"strand":1,"feature_type":"variation","id":"rs1019660397","seq_region_name":"7","clinical_significance":[]},{"id":"rs1327769029","seq_region_name":"7","clinical_significance":[],"start":140479084,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140479091,"alleles":["CCTCCTCC","CCTCC"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479086,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140479086,"clinical_significance":[],"id":"rs1349443586","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1400986122","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479090,"feature_type":"variation","strand":1,"end":140479090,"alleles":["C","A"]},{"seq_region_name":"7","id":"rs976366087","clinical_significance":[],"end":140479092,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140479092,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140479092,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140479108,"alleles":["CTCCCGCGCCGCAGGCT","CT"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2045251191","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140479093,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140479093,"source":"dbSNP","seq_region_name":"7","id":"rs879754601","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs932433943","feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140479094,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479094},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479095,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140479095,"clinical_significance":[],"seq_region_name":"7","id":"rs1585506582"},{"end":140479105,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140479105,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1238690216","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795211560","clinical_significance":[],"end":140479106,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140479106,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140479110,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140479110,"id":"rs1220800200","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1397443991","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479111,"feature_type":"variation","strand":1,"end":140479111,"alleles":["G","A"]},{"end":140479112,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140479112,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs985170766"},{"start":140479112,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140479114,"alleles":["CCC","CC"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs746143193","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140479114,"source":"dbSNP","strand":1,"feature_type":"variation","end":140479114,"alleles":["C","T"],"seq_region_name":"7","id":"rs1477984894","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1307395572","alleles":["G","A"],"end":140479115,"feature_type":"variation","strand":1,"source":"dbSNP","start":140479115,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140479117,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479117,"clinical_significance":[],"seq_region_name":"7","id":"rs997441237"},{"clinical_significance":[],"seq_region_name":"7","id":"rs573211181","end":140479118,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140479118,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs969277812","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479119,"feature_type":"variation","strand":1,"end":140479119,"alleles":["C","A"]},{"id":"rs1585506657","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140479119,"source":"dbSNP","strand":1,"feature_type":"variation","end":140479134,"alleles":["CCCCCTCCCCGCGCCC","CCCCCTCCCCGCGCCCCCCTCCCCGCGCCC"]},{"clinical_significance":[],"id":"rs946505986","seq_region_name":"7","alleles":["C","A"],"end":140479120,"feature_type":"variation","strand":1,"source":"dbSNP","start":140479120,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","A"],"end":140479122,"strand":1,"feature_type":"variation","start":140479122,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795212242","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140479123,"source":"dbSNP","strand":1,"feature_type":"variation","end":140479123,"alleles":["C","T"],"seq_region_name":"7","id":"rs979040213","clinical_significance":[]},{"start":140479124,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140479124,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs933591233","clinical_significance":[]},{"end":140479125,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140479125,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795212415","seq_region_name":"7"},{"seq_region_name":"7","id":"rs924851479","clinical_significance":[],"strand":1,"feature_type":"variation","end":140479128,"alleles":["CCCC","CCC"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140479125,"source":"dbSNP"},{"seq_region_name":"7","id":"rs747526366","clinical_significance":[],"start":140479127,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140479127,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"alleles":["C","A","G"],"end":140479128,"strand":1,"feature_type":"variation","start":140479128,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs902404161","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140479131,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140479131,"seq_region_name":"7","id":"rs1208112064","clinical_significance":[]},{"end":140479132,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140479132,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1349413316","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130386079","feature_type":"variation","strand":1,"end":140479135,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479135},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795212778","feature_type":"variation","strand":1,"end":140479138,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479138},{"clinical_significance":[],"id":"rs1210440558","seq_region_name":"7","source":"dbSNP","start":140479140,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140479140,"alleles":["T","C"],"feature_type":"variation","strand":1},{"start":140479142,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","T"],"end":140479142,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs934691793","clinical_significance":[]},{"start":140479145,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140479145,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs917673605","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479146,"feature_type":"variation","strand":1,"end":140479146,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs949142658"},{"clinical_significance":[],"seq_region_name":"7","id":"rs570173552","alleles":["G","A"],"end":140479148,"feature_type":"variation","strand":1,"source":"dbSNP","start":140479148,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140479150,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479150,"clinical_significance":[],"seq_region_name":"7","id":"rs1239096774"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1172148420","feature_type":"variation","strand":1,"end":140479151,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479151},{"alleles":["C","A","T"],"end":140479152,"strand":1,"feature_type":"variation","start":140479152,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_region_variant","seq_region_name":"7","id":"rs540731213","clinical_significance":[]},{"start":140479153,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_region_variant","end":140479153,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs779106753","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"splice_donor_region_variant","start":140479154,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","G"],"end":140479154,"seq_region_name":"7","id":"rs1585506765","clinical_significance":[]},{"seq_region_name":"7","id":"rs1186620267","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140479157,"assembly_name":"GRCh38","consequence_type":"splice_donor_region_variant","start":140479157,"source":"dbSNP"},{"end":140479159,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140479159,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_donor_variant","id":"rs1176789228","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs931141195","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479163,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140479163},{"seq_region_name":"7","id":"rs1795213686","clinical_significance":[],"strand":1,"feature_type":"variation","end":140479165,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140479165,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795213741","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140479167,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479167},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479171,"feature_type":"variation","strand":1,"end":140479171,"alleles":["C","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1360832538"},{"seq_region_name":"7","id":"rs1192575951","clinical_significance":["uncertain significance"],"alleles":["T","C"],"end":140479172,"strand":1,"feature_type":"variation","start":140479172,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"alleles":["G","T"],"end":140479173,"feature_type":"variation","strand":1,"source":"dbSNP","start":140479173,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1219203498"},{"clinical_significance":[],"seq_region_name":"7","id":"rs748568314","feature_type":"variation","strand":1,"end":140479175,"alleles":["T","C"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479175},{"seq_region_name":"7","id":"rs1312373651","clinical_significance":[],"start":140479176,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140479176,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1585506826","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["CCAGCCGCC","-"],"end":140479188,"assembly_name":"GRCh38","consequence_type":"inframe_deletion","start":140479180,"source":"dbSNP"},{"seq_region_name":"7","id":"rs756250337","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"inframe_insertion","start":140479183,"source":"dbSNP","strand":1,"feature_type":"variation","end":140479193,"alleles":["GCCGCCGCCGC","GCCGCCGC","GCCGCCGCCGCCGC"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795214642","alleles":["GCCGCCGCCGCTGCCGTCGCTGCCGCCGCC","GCCGCCGCC"],"end":140479212,"feature_type":"variation","strand":1,"source":"dbSNP","start":140479183,"consequence_type":"inframe_deletion","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795214719","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"inframe_insertion","start":140479186,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GCCGCCGCTGCCG","GCCGCCGCTGCCGCCGCTGCCG"],"end":140479198},{"clinical_significance":[],"seq_region_name":"7","id":"rs1361369501","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479188,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140479188},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140479189,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479189,"clinical_significance":[],"seq_region_name":"7","id":"rs1175681077"},{"source":"dbSNP","start":140479190,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140479190,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1402125968"},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140479191,"source":"dbSNP","strand":1,"feature_type":"variation","end":140479191,"alleles":["C","T"],"seq_region_name":"7","id":"rs1013045830","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs780350644","consequence_type":"protein_altering_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479191,"feature_type":"variation","strand":1,"alleles":["CGCTGCCGTCGCTGCCG","CGCTGCCGTCGCTGCCGTCGCTGCCG"],"end":140479207},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479194,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140479194,"clinical_significance":[],"seq_region_name":"7","id":"rs1795215153"},{"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479195,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140479195,"clinical_significance":[],"id":"rs1361770336","seq_region_name":"7"},{"id":"rs1273565702","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["GCCGTCGCTGCCGCCG","GCCGTCGCTGCCGCCGTCGCTGCCGCCG"],"end":140479210,"assembly_name":"GRCh38","consequence_type":"inframe_insertion","start":140479195,"source":"dbSNP"},{"seq_region_name":"7","id":"rs772125991","clinical_significance":[],"start":140479197,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["C","G"],"end":140479197,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1041025000","seq_region_name":"7","source":"dbSNP","start":140479199,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140479199,"alleles":["T","C"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140479200,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140479200,"seq_region_name":"7","id":"rs778058982","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1277640284","end":140479211,"alleles":["CGCTGCCGCCGC","CGC","CGCTGCCGCCGCTGCCGCCGC"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140479200,"consequence_type":"inframe_deletion","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140479204,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140479204,"id":"rs558648072","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140479204,"consequence_type":"inframe_insertion","assembly_name":"GRCh38","end":140479212,"alleles":["GCCGCCGCC","GCCGCCGCCGCCGCCGCC"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795215789"},{"clinical_significance":["uncertain significance"],"id":"rs1357580673","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140479206,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479206},{"end":140479207,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140479207,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1279039287","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1447698458","alleles":["C","T"],"end":140479211,"feature_type":"variation","strand":1,"source":"dbSNP","start":140479211,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140479211,"consequence_type":"frameshift_variant","assembly_name":"GRCh38","end":140479215,"alleles":["CCCCC","CCCC"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1488398510"},{"clinical_significance":["uncertain significance"],"seq_region_name":"7","id":"rs1355639273","alleles":["C","T"],"end":140479212,"feature_type":"variation","strand":1,"source":"dbSNP","start":140479212,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"consequence_type":"frameshift_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479213,"feature_type":"variation","strand":1,"end":140479222,"alleles":["CCCTCCGCCC","CCC"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795216144"},{"seq_region_name":"7","id":"rs1795216204","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140479215,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140479215,"source":"dbSNP"},{"alleles":["C","T"],"end":140479218,"strand":1,"feature_type":"variation","start":140479218,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs1218405254","clinical_significance":[]},{"consequence_type":"inframe_insertion","assembly_name":"GRCh38","source":"dbSNP","start":140479220,"feature_type":"variation","strand":1,"alleles":["CCC","CCCCCC"],"end":140479222,"clinical_significance":[],"seq_region_name":"7","id":"rs1240139362"},{"strand":1,"feature_type":"variation","alleles":["G","A","C","T"],"end":140479223,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140479223,"source":"dbSNP","seq_region_name":"7","id":"rs770987129","clinical_significance":[]},{"seq_region_name":"7","id":"rs1173082510","clinical_significance":[],"end":140479224,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140479224,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140479225,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479225,"clinical_significance":[],"id":"rs1408712595","seq_region_name":"7"},{"alleles":["C","T"],"end":140479228,"strand":1,"feature_type":"variation","start":140479228,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","seq_region_name":"7","id":"rs776740671","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140479229,"source":"dbSNP","strand":1,"feature_type":"variation","end":140479229,"alleles":["A","C"],"seq_region_name":"7","id":"rs528273101","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1427116232","end":140479231,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140479231,"consequence_type":"synonymous_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs888630935","seq_region_name":"7","source":"dbSNP","start":140479232,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140479232,"alleles":["G","A","T"],"feature_type":"variation","strand":1},{"id":"rs1169319017","seq_region_name":"7","clinical_significance":[],"end":140479235,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140479235,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"start":140479236,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["G","A"],"end":140479236,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs901150933","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1006095959","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140479238,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479238},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140479239,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479239,"clinical_significance":[],"id":"rs1475355571","seq_region_name":"7"},{"id":"rs762846600","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140479240,"source":"dbSNP","strand":1,"feature_type":"variation","end":140479240,"alleles":["G","A","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130386643","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479242,"feature_type":"variation","strand":1,"end":140479242,"alleles":["T","G"]},{"seq_region_name":"7","id":"rs1173054220","clinical_significance":[],"start":140479243,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","end":140479243,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":["uncertain significance"],"seq_region_name":"7","id":"rs768673416","end":140479245,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140479245,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140479246,"consequence_type":"frameshift_variant","assembly_name":"GRCh38","end":140479249,"alleles":["TGTG","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795218259","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795218324","feature_type":"variation","strand":1,"end":140479247,"alleles":["G","A"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479247},{"end":140479248,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140479248,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs961903306"},{"clinical_significance":["uncertain significance"],"seq_region_name":"7","id":"rs773972832","source":"dbSNP","start":140479251,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140479251,"alleles":["G","C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1585507076","clinical_significance":["likely benign"],"start":140479255,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","end":140479255,"alleles":["C","A","T"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140479256,"source":"dbSNP","strand":1,"feature_type":"variation","end":140479256,"alleles":["G","A","C","T"],"seq_region_name":"7","id":"rs200911173","clinical_significance":["uncertain significance"]},{"alleles":["G","A"],"end":140479257,"strand":1,"feature_type":"variation","start":140479257,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs1795218748","clinical_significance":[]},{"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479258,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140479258,"clinical_significance":[],"id":"rs1344839510","seq_region_name":"7"},{"id":"rs889148960","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140479260,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140479260,"source":"dbSNP"},{"clinical_significance":[],"id":"rs542039727","seq_region_name":"7","consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479261,"feature_type":"variation","strand":1,"alleles":["G","A","C","T"],"end":140479261},{"consequence_type":"frameshift_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479261,"feature_type":"variation","strand":1,"end":140479265,"alleles":["GGGGG","GGGG"],"clinical_significance":[],"seq_region_name":"7","id":"rs1437563916"},{"clinical_significance":[],"id":"rs1563100422","seq_region_name":"7","consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479264,"feature_type":"variation","strand":1,"end":140479264,"alleles":["G","A"]},{"feature_type":"variation","strand":1,"end":140479265,"alleles":["G","A","T"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479265,"clinical_significance":["uncertain significance"],"seq_region_name":"7","id":"rs765951978"},{"seq_region_name":"7","id":"rs1234260868","clinical_significance":[],"start":140479266,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["A","G"],"end":140479266,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs953703843","source":"dbSNP","start":140479267,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","end":140479267,"alleles":["G","A","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1353875469","alleles":["G","C"],"end":140479268,"feature_type":"variation","strand":1,"source":"dbSNP","start":140479268,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"inframe_deletion","start":140479268,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GCTGCTGC","GCTGC"],"end":140479275,"seq_region_name":"7","id":"rs1228113665","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140479269,"source":"dbSNP","strand":1,"feature_type":"variation","end":140479269,"alleles":["C","G","T"],"seq_region_name":"7","id":"rs917617233","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795219679","clinical_significance":[],"alleles":["T","C"],"end":140479270,"strand":1,"feature_type":"variation","start":140479270,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant"},{"alleles":["G","A"],"end":140479271,"feature_type":"variation","strand":1,"source":"dbSNP","start":140479271,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs753428863","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795219803","clinical_significance":[],"start":140479272,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140479272,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"end":140479273,"alleles":["T","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140479273,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1281627946"},{"clinical_significance":[],"id":"rs1795220004","seq_region_name":"7","feature_type":"variation","strand":1,"end":140479274,"alleles":["G","A"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479274},{"clinical_significance":[],"seq_region_name":"7","id":"rs368688966","alleles":["C","G","T"],"end":140479276,"feature_type":"variation","strand":1,"source":"dbSNP","start":140479276,"consequence_type":"synonymous_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795220160","source":"dbSNP","start":140479276,"consequence_type":"inframe_insertion","assembly_name":"GRCh38","end":140479286,"alleles":["CGCCGTCGCCG","CGCCGTCGCCGTCGCCG"],"feature_type":"variation","strand":1},{"alleles":["G","C"],"end":140479277,"feature_type":"variation","strand":1,"source":"dbSNP","start":140479277,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1221976155","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1248285966","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140479279,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140479279},{"end":140479280,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140479280,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs980582271"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795220416","consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479282,"feature_type":"variation","strand":1,"end":140479282,"alleles":["C","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1554451679","feature_type":"variation","strand":1,"alleles":["CGCCGC","CGCCGCCGC"],"end":140479287,"consequence_type":"inframe_insertion","assembly_name":"GRCh38","source":"dbSNP","start":140479282},{"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140479283,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140479283,"source":"dbSNP","id":"rs1467068819","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1419586706","consequence_type":"inframe_insertion","assembly_name":"GRCh38","source":"dbSNP","start":140479283,"feature_type":"variation","strand":1,"alleles":["GCCGCTGCCGCT","GCCGCT","GCCGCTGCCGCTGCCGCT"],"end":140479294},{"source":"dbSNP","start":140479284,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140479284,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795220695"},{"consequence_type":"inframe_deletion","assembly_name":"GRCh38","source":"dbSNP","start":140479284,"feature_type":"variation","strand":1,"end":140479296,"alleles":["CCGCTGCCGCTCC","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795220753"},{"seq_region_name":"7","id":"rs374472977","clinical_significance":["uncertain significance"],"start":140479286,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140479286,"alleles":["G","A","C","T"],"strand":1,"feature_type":"variation"},{"end":140479287,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140479287,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs1795220955","clinical_significance":[]},{"alleles":["T","A"],"end":140479288,"strand":1,"feature_type":"variation","start":140479288,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","seq_region_name":"7","id":"rs1238862358","clinical_significance":[]},{"source":"dbSNP","start":140479289,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140479289,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs758786694"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1457592414","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479290,"feature_type":"variation","strand":1,"end":140479290,"alleles":["C","A","T"]},{"seq_region_name":"7","id":"rs931152624","clinical_significance":[],"strand":1,"feature_type":"variation","end":140479291,"alleles":["C","A","G","T"],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140479291,"source":"dbSNP"},{"id":"rs199946433","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140479292,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140479292},{"end":140479304,"alleles":["GCTCCTGCTCCTG","GCTCCTG"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140479292,"consequence_type":"inframe_deletion","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1563100501"},{"feature_type":"variation","strand":1,"alleles":["C","A","G","T"],"end":140479295,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479295,"clinical_significance":[],"id":"rs939963126","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140479297,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140479297,"source":"dbSNP","id":"rs978299746","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1041346542","clinical_significance":[],"strand":1,"feature_type":"variation","end":140479298,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140479298,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140479299,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140479299,"source":"dbSNP","seq_region_name":"7","id":"rs1795221885","clinical_significance":[]},{"seq_region_name":"7","id":"rs189817584","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140479300,"source":"dbSNP","strand":1,"feature_type":"variation","end":140479300,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs369712962","end":140479301,"alleles":["C","A","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140479301,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1441006044","seq_region_name":"7","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479302,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140479302},{"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140479303,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479303,"clinical_significance":[],"seq_region_name":"7","id":"rs1795222182"},{"clinical_significance":[],"seq_region_name":"7","id":"rs749334129","end":140479311,"alleles":["TGTTGT","TGT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140479306,"consequence_type":"inframe_deletion","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs904572315","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140479307,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479307},{"seq_region_name":"7","id":"rs1457135327","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140479309,"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140479309,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140479310,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479310,"clinical_significance":["uncertain significance"],"seq_region_name":"7","id":"rs1345383434"},{"clinical_significance":["uncertain significance"],"seq_region_name":"7","id":"rs1430580572","source":"dbSNP","start":140479311,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140479311,"alleles":["T","C"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140479312,"alleles":["G","C"],"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479312,"clinical_significance":[],"seq_region_name":"7","id":"rs1440809016"},{"clinical_significance":["uncertain significance"],"seq_region_name":"7","id":"rs1171646602","end":140479314,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140479314,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"alleles":["T","C"],"end":140479315,"feature_type":"variation","strand":1,"source":"dbSNP","start":140479315,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1379620238"},{"strand":1,"feature_type":"variation","alleles":["TG","TGGTG"],"end":140479316,"assembly_name":"GRCh38","consequence_type":"inframe_insertion","start":140479315,"source":"dbSNP","seq_region_name":"7","id":"rs1554451708","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs142316327","end":140479316,"alleles":["G","GGGG"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140479316,"consequence_type":"inframe_insertion","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1332552486","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479316,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140479316},{"clinical_significance":[],"seq_region_name":"7","id":"rs781213059","source":"dbSNP","start":140479317,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140479317,"alleles":["T","C","G"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140479318,"alleles":["T","G"],"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479318,"clinical_significance":[],"seq_region_name":"7","id":"rs1563100564"},{"feature_type":"variation","strand":1,"end":140479319,"alleles":["G","C","T"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479319,"clinical_significance":[],"id":"rs1443680161","seq_region_name":"7"},{"alleles":["T","A"],"end":140479320,"feature_type":"variation","strand":1,"source":"dbSNP","start":140479320,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs546690208"},{"end":140479322,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140479322,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","id":"rs1056393310","seq_region_name":"7","clinical_significance":["uncertain significance"]},{"source":"dbSNP","start":140479323,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140479323,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795223522"},{"source":"dbSNP","start":140479325,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140479325,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs564697889"},{"id":"rs1795223760","seq_region_name":"7","clinical_significance":[],"start":140479326,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140479326,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140479329,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140479329,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130387492"},{"seq_region_name":"7","id":"rs895854476","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140479332,"source":"dbSNP","strand":1,"feature_type":"variation","end":140479332,"alleles":["C","T"]},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140479334,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140479334,"seq_region_name":"7","id":"rs948667095","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140479335,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140479335,"source":"dbSNP","seq_region_name":"7","id":"rs1795224062","clinical_significance":[]},{"end":140479336,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140479336,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","seq_region_name":"7","id":"rs1265421505","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795224276","consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479339,"feature_type":"variation","strand":1,"end":140479339,"alleles":["C","T"]},{"consequence_type":"start_lost","assembly_name":"GRCh38","source":"dbSNP","start":140479342,"feature_type":"variation","strand":1,"end":140479342,"alleles":["C","T"],"clinical_significance":[],"id":"rs1209287756","seq_region_name":"7"},{"consequence_type":"start_lost","assembly_name":"GRCh38","source":"dbSNP","start":140479344,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140479344,"clinical_significance":[],"seq_region_name":"7","id":"rs1486336656"},{"source":"dbSNP","start":140479346,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","end":140479346,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1262666747","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs532167277","alleles":["T","A"],"end":140479348,"feature_type":"variation","strand":1,"source":"dbSNP","start":140479348,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38"},{"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479350,"feature_type":"variation","strand":1,"end":140479350,"alleles":["T","C"],"clinical_significance":[],"id":"rs1795224780","seq_region_name":"7"},{"id":"rs1795224874","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","start":140479358,"source":"dbSNP","strand":1,"feature_type":"variation","end":140479358,"alleles":["A","G","T"]},{"alleles":["C","A","G"],"end":140479361,"strand":1,"feature_type":"variation","start":140479361,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","seq_region_name":"7","id":"rs1000380284","clinical_significance":[]},{"source":"dbSNP","start":140479364,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140479364,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs745972902"},{"alleles":["A","G"],"end":140479366,"strand":1,"feature_type":"variation","start":140479366,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","seq_region_name":"7","id":"rs1795225168","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795225243","feature_type":"variation","strand":1,"alleles":["A","T"],"end":140479367,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479367},{"source":"dbSNP","start":140479369,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","end":140479369,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1353353070","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795225409","clinical_significance":[],"start":140479370,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","alleles":["C","A"],"end":140479370,"strand":1,"feature_type":"variation"},{"end":140479371,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140479371,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795225498"},{"seq_region_name":"7","id":"rs1281484600","clinical_significance":[],"start":140479373,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","end":140479373,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1332496787","consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479374,"feature_type":"variation","strand":1,"end":140479374,"alleles":["G","A","C"]},{"seq_region_name":"7","id":"rs1795225771","clinical_significance":[],"start":140479375,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","alleles":["G","C"],"end":140479375,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140479376,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","end":140479376,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130387697"},{"source":"dbSNP","start":140479377,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140479377,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1464891538"},{"alleles":["C","A"],"end":140479378,"strand":1,"feature_type":"variation","start":140479378,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","id":"rs1237217438","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130387725","end":140479379,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140479379,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140479382,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479382,"clinical_significance":[],"seq_region_name":"7","id":"rs1044503245"},{"source":"dbSNP","start":140479384,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140479384,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1329832552"},{"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140479385,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479385,"clinical_significance":[],"seq_region_name":"7","id":"rs888507374"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1385693033","alleles":["A","T"],"end":140479391,"feature_type":"variation","strand":1,"source":"dbSNP","start":140479391,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1362244181","consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479392,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140479392},{"seq_region_name":"7","id":"rs1795226206","clinical_significance":[],"alleles":["G","A"],"end":140479399,"strand":1,"feature_type":"variation","start":140479399,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant"},{"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479400,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140479400,"clinical_significance":[],"seq_region_name":"7","id":"rs1795226263"},{"clinical_significance":[],"id":"rs780744521","seq_region_name":"7","end":140479401,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140479401,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38"},{"end":140479402,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140479402,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1005733932"},{"start":140479403,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","end":140479403,"alleles":["C","A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795226455","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","start":140479408,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GCGGGGAGAGG","GCGGGGAGAGGGCGGGGAGAGG"],"end":140479418,"seq_region_name":"7","id":"rs1795226504","clinical_significance":[]},{"start":140479409,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","alleles":["C","T"],"end":140479409,"strand":1,"feature_type":"variation","id":"rs1031821657","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795226647","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140479410,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479410},{"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479411,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140479411,"clinical_significance":[],"id":"rs891953061","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1016207967","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","start":140479412,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140479412},{"feature_type":"variation","strand":1,"alleles":["G","A","C","T"],"end":140479413,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479413,"clinical_significance":[],"seq_region_name":"7","id":"rs1024970835"},{"alleles":["G","A"],"end":140479415,"strand":1,"feature_type":"variation","start":140479415,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","id":"rs897305582","seq_region_name":"7","clinical_significance":[]},{"id":"rs1795226988","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140479416,"assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","start":140479416,"source":"dbSNP"},{"alleles":["G","A"],"end":140479418,"strand":1,"feature_type":"variation","start":140479418,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","seq_region_name":"7","id":"rs1563100650","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs550884706","alleles":["C","A","T"],"end":140479420,"feature_type":"variation","strand":1,"source":"dbSNP","start":140479420,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["G","C","T"],"end":140479421,"assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","start":140479421,"source":"dbSNP","id":"rs1795227150","seq_region_name":"7","clinical_significance":[]},{"start":140479422,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","end":140479422,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1307451524","clinical_significance":[]},{"source":"dbSNP","start":140479423,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140479423,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs998424717","seq_region_name":"7"},{"source":"dbSNP","start":140479427,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140479427,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs980807046","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1033398235","consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479430,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140479430},{"clinical_significance":[],"seq_region_name":"7","id":"rs1191855397","feature_type":"variation","strand":1,"alleles":["AGGCGAGG","AGG"],"end":140479437,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479430},{"assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","start":140479431,"source":"dbSNP","strand":1,"feature_type":"variation","end":140479431,"alleles":["G","A"],"seq_region_name":"7","id":"rs1488077138","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795227569","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140479436,"assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","start":140479436,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1281552489","clinical_significance":[],"end":140479437,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140479437,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant"},{"start":140479440,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","end":140479440,"alleles":["A","G"],"strand":1,"feature_type":"variation","id":"rs1585507616","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140479441,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479441,"clinical_significance":[],"seq_region_name":"7","id":"rs1029834104"},{"seq_region_name":"7","id":"rs1585507620","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","start":140479442,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140479442},{"seq_region_name":"7","id":"rs953715157","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","start":140479443,"source":"dbSNP","strand":1,"feature_type":"variation","end":140479443,"alleles":["G","C"]},{"seq_region_name":"7","id":"rs1006487287","clinical_significance":[],"strand":1,"feature_type":"variation","end":140479447,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","start":140479447,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["A","C","T"],"end":140479451,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479451,"clinical_significance":[],"seq_region_name":"7","id":"rs12539598"},{"seq_region_name":"7","id":"rs1022057746","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140479452,"assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","start":140479452,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","start":140479453,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140479453,"id":"rs1307641630","seq_region_name":"7","clinical_significance":[]},{"end":140479454,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140479454,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","seq_region_name":"7","id":"rs1585507658","clinical_significance":[]},{"id":"rs968230316","seq_region_name":"7","clinical_significance":[],"end":140479457,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140479457,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant"},{"seq_region_name":"7","id":"rs1795228272","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","start":140479458,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140479458},{"clinical_significance":[],"id":"rs1053892158","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140479459,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479459},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795228387","alleles":["C","G","T"],"end":140479460,"feature_type":"variation","strand":1,"source":"dbSNP","start":140479460,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","start":140479461,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140479461,"seq_region_name":"7","id":"rs977849614","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1486585625","source":"dbSNP","start":140479464,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","end":140479464,"alleles":["T","C"],"feature_type":"variation","strand":1},{"alleles":["T","C","G"],"end":140479465,"strand":1,"feature_type":"variation","start":140479465,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","id":"rs1795228595","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140479466,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","start":140479466,"source":"dbSNP","id":"rs1397514466","seq_region_name":"7","clinical_significance":[]},{"id":"rs150126646","seq_region_name":"7","clinical_significance":[],"start":140479467,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","alleles":["G","C","T"],"end":140479467,"strand":1,"feature_type":"variation"},{"alleles":["T","G"],"end":140479469,"strand":1,"feature_type":"variation","start":140479469,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","id":"rs536555446","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","start":140479470,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140479470,"seq_region_name":"7","id":"rs1795228836","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795228889","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["CCCC","CCC"],"end":140479473,"assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","start":140479470,"source":"dbSNP"},{"seq_region_name":"7","id":"rs548366578","clinical_significance":[],"start":140479471,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","end":140479471,"alleles":["C","G","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs916463086","clinical_significance":[],"start":140479472,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","end":140479472,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1477640427","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140479473,"assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","start":140479473,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140479474,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479474,"clinical_significance":[],"seq_region_name":"7","id":"rs1258441413"},{"id":"rs566676137","seq_region_name":"7","clinical_significance":[],"alleles":["C","G"],"end":140479476,"strand":1,"feature_type":"variation","start":140479476,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant"},{"source":"dbSNP","start":140479480,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","end":140479480,"alleles":["T","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1440983898"},{"seq_region_name":"7","id":"rs1795229277","clinical_significance":[],"alleles":["C","T"],"end":140479482,"strand":1,"feature_type":"variation","start":140479482,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant"},{"seq_region_name":"7","id":"rs534011735","clinical_significance":[],"alleles":["G","A","T"],"end":140479483,"strand":1,"feature_type":"variation","start":140479483,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1196945405","end":140479484,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140479484,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38"},{"alleles":["G","A"],"end":140479485,"strand":1,"feature_type":"variation","start":140479485,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","seq_region_name":"7","id":"rs1050161434","clinical_significance":[]},{"start":140479488,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","end":140479488,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1259480593","clinical_significance":[]},{"seq_region_name":"7","id":"rs576499628","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","start":140479490,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140479490},{"source":"dbSNP","start":140479491,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140479491,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs904627942"},{"id":"rs1795229697","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140479492,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","start":140479492,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795229760","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140479493,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479493},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140479494,"assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","start":140479494,"source":"dbSNP","seq_region_name":"7","id":"rs1795229808","clinical_significance":[]},{"source":"dbSNP","start":140479500,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","end":140479500,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795229865"},{"source":"dbSNP","start":140479501,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140479501,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1293470491"},{"end":140479503,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140479503,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","seq_region_name":"7","id":"rs1246721001","clinical_significance":[]},{"start":140479505,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","end":140479505,"alleles":["C","A","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1433849620","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130388358","consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479506,"feature_type":"variation","strand":1,"end":140479505,"alleles":["-","CCCTCTCCTCTTCTTATAGGGGCAAAAATCATTGGATTTAGG"]},{"seq_region_name":"7","id":"rs1044764238","clinical_significance":[],"end":140479506,"alleles":["G","C","T"],"strand":1,"feature_type":"variation","start":140479506,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant"},{"assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","start":140479507,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140479507,"seq_region_name":"7","id":"rs1585507807","clinical_significance":[]},{"id":"rs2130388385","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","start":140479509,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["-","TTTCCTAATCCAATATGGCTGTTATA"],"end":140479508},{"clinical_significance":[],"id":"rs1795230278","seq_region_name":"7","consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479509,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140479509},{"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479509,"feature_type":"variation","strand":1,"alleles":["A","-"],"end":140479509,"clinical_significance":[],"seq_region_name":"7","id":"rs2130388401"},{"seq_region_name":"7","id":"rs909873257","clinical_significance":[],"strand":1,"feature_type":"variation","end":140479510,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","start":140479510,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795230374","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","start":140479516,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140479516},{"source":"dbSNP","start":140479517,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","end":140479516,"alleles":["-","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1391942021"},{"id":"rs941468795","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140479517,"alleles":["T","C","G"],"assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","start":140479517,"source":"dbSNP"},{"start":140479517,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","alleles":["TGCGGGCCCAGAGCATGCG","TGCGGGCCCAGAGCATGCGGGCCCAGAGCATGCG"],"end":140479535,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795230532","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","start":140479518,"source":"dbSNP","strand":1,"feature_type":"variation","end":140479518,"alleles":["G","T"],"seq_region_name":"7","id":"rs1402329970","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","A","G"],"end":140479519,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479519,"clinical_significance":[],"seq_region_name":"7","id":"rs117397064"},{"seq_region_name":"7","id":"rs1465124910","clinical_significance":[],"strand":1,"feature_type":"variation","end":140479520,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","start":140479520,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1418864147","feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140479521,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479521},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795230832","consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479522,"feature_type":"variation","strand":1,"end":140479540,"alleles":["GCCCAGAGCATGCGCGCCC","GCCCAGAGCATGCGCGCCCAGAGCATGCGCGCCC"]},{"seq_region_name":"7","id":"rs1053182485","clinical_significance":[],"end":140479523,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140479523,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795230925","consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479524,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140479524},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140479525,"assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","start":140479525,"source":"dbSNP","id":"rs1795230977","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1346048543","end":140479526,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140479526,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795231082","end":140479527,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140479527,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795231127","clinical_significance":[],"start":140479528,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","end":140479528,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"alleles":["G","A","C"],"end":140479529,"strand":1,"feature_type":"variation","start":140479529,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","seq_region_name":"7","id":"rs546359738","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1182946787","consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479531,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140479531},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130388566","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140479532,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479532},{"seq_region_name":"7","id":"rs760215848","clinical_significance":[],"strand":1,"feature_type":"variation","end":140479538,"alleles":["GCGCGC","GCGC"],"assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","start":140479533,"source":"dbSNP"},{"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479535,"feature_type":"variation","strand":1,"end":140479535,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1236837222"},{"feature_type":"variation","strand":1,"end":140479537,"alleles":["G","A","T"],"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479537,"clinical_significance":[],"id":"rs1361285442","seq_region_name":"7"},{"source":"dbSNP","start":140479538,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","end":140479538,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585507888"},{"clinical_significance":[],"seq_region_name":"7","id":"rs537887239","source":"dbSNP","start":140479540,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","end":140479540,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795231577","clinical_significance":[],"alleles":["G","A"],"end":140479541,"strand":1,"feature_type":"variation","start":140479541,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant"},{"start":140479542,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","alleles":["C","A","G"],"end":140479542,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1051303035","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140479543,"alleles":["G","C"],"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479543,"clinical_significance":[],"seq_region_name":"7","id":"rs556433969"},{"feature_type":"variation","strand":1,"end":140479546,"alleles":["C","T"],"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479546,"clinical_significance":[],"seq_region_name":"7","id":"rs890014350"},{"clinical_significance":[],"id":"rs1795231820","seq_region_name":"7","source":"dbSNP","start":140479547,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140479547,"feature_type":"variation","strand":1},{"start":140479549,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","end":140479549,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs906076541","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1283420646","alleles":["A","G"],"end":140479552,"feature_type":"variation","strand":1,"source":"dbSNP","start":140479552,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140479553,"alleles":["C","T"],"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479553,"clinical_significance":[],"seq_region_name":"7","id":"rs1239448323"},{"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479554,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140479554,"clinical_significance":[],"seq_region_name":"7","id":"rs1795232072"},{"clinical_significance":[],"id":"rs1007079082","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140479555,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479555},{"alleles":["C","A"],"end":140479559,"feature_type":"variation","strand":1,"source":"dbSNP","start":140479559,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795232174","seq_region_name":"7"},{"id":"rs1022408361","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140479563,"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140479563,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795232290","source":"dbSNP","start":140479571,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","end":140479571,"alleles":["G","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1001890946","seq_region_name":"7","consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479572,"feature_type":"variation","strand":1,"end":140479572,"alleles":["A","G"]},{"start":140479577,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","end":140479577,"alleles":["A","-"],"strand":1,"feature_type":"variation","id":"rs1033329372","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","T"],"end":140479577,"strand":1,"feature_type":"variation","start":140479577,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","seq_region_name":"7","id":"rs1795232527","clinical_significance":[]},{"alleles":["C","T"],"end":140479578,"feature_type":"variation","strand":1,"source":"dbSNP","start":140479578,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs11981376"},{"clinical_significance":[],"id":"rs1585507949","seq_region_name":"7","consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479579,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140479579},{"alleles":["T","G"],"end":140479580,"strand":1,"feature_type":"variation","start":140479580,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","id":"rs1395388074","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795232844","source":"dbSNP","start":140479581,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","alleles":["CTCCTCC","CTCC"],"end":140479587,"feature_type":"variation","strand":1},{"start":140479582,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","alleles":["T","C","G"],"end":140479582,"strand":1,"feature_type":"variation","id":"rs1285341143","seq_region_name":"7","clinical_significance":[]},{"end":140479583,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140479583,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","seq_region_name":"7","id":"rs1795232986","clinical_significance":[]},{"source":"dbSNP","start":140479584,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140479584,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795233033"},{"clinical_significance":[],"seq_region_name":"7","id":"rs746023858","alleles":["T","C","G"],"end":140479585,"feature_type":"variation","strand":1,"source":"dbSNP","start":140479585,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140479586,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140479586,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795233171"},{"seq_region_name":"7","id":"rs1213141048","clinical_significance":[],"strand":1,"feature_type":"variation","end":140479587,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140479587,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1441871386","clinical_significance":[],"start":140479588,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","alleles":["G","A"],"end":140479588,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1015293983","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140479589,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479589},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795233430","feature_type":"variation","strand":1,"end":140479597,"alleles":["C","T"],"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479597},{"seq_region_name":"7","id":"rs1795233479","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140479600,"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140479600,"source":"dbSNP"},{"source":"dbSNP","start":140479602,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","alleles":["C","-"],"end":140479602,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1178632397"},{"start":140479602,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","alleles":["C","A"],"end":140479602,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795233529","clinical_significance":[]},{"start":140479605,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","alleles":["A","G"],"end":140479605,"strand":1,"feature_type":"variation","id":"rs961237015","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1200331018","source":"dbSNP","start":140479606,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","end":140479606,"alleles":["C","T"],"feature_type":"variation","strand":1},{"id":"rs1288640937","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140479607,"strand":1,"feature_type":"variation","start":140479607,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant"},{"seq_region_name":"7","id":"rs1246831738","clinical_significance":[],"start":140479607,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","end":140479611,"alleles":["GGGGG","GGG","GGGGGG"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1259632477","clinical_significance":[],"alleles":["G","A","C"],"end":140479609,"strand":1,"feature_type":"variation","start":140479609,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant"},{"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140479610,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140479610,"seq_region_name":"7","id":"rs1030710065","clinical_significance":[]},{"id":"rs960536980","seq_region_name":"7","clinical_significance":[],"end":140479611,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140479611,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant"},{"id":"rs1585508045","seq_region_name":"7","clinical_significance":[],"end":140479612,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140479612,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant"},{"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140479613,"source":"dbSNP","strand":1,"feature_type":"variation","end":140479613,"alleles":["C","T"],"id":"rs991961769","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140479615,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","end":140479615,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795234171","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs542125103","alleles":["A","G","T"],"end":140479619,"feature_type":"variation","strand":1,"source":"dbSNP","start":140479619,"consequence_type":"TF_binding_site_variant","assembly_name":"GRCh38"},{"end":140479619,"alleles":["A","-"],"strand":1,"feature_type":"variation","start":140479619,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","seq_region_name":"7","id":"rs1795234319","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140479621,"consequence_type":"TF_binding_site_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479621,"clinical_significance":[],"seq_region_name":"7","id":"rs1795234361"},{"assembly_name":"GRCh38","consequence_type":"TF_binding_site_variant","start":140479623,"source":"dbSNP","strand":1,"feature_type":"variation","end":140479623,"alleles":["G","A"],"seq_region_name":"7","id":"rs1795234410","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140479626,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479626,"clinical_significance":[],"id":"rs1795234462","seq_region_name":"7"},{"seq_region_name":"7","id":"rs761706801","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140479627,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140479627},{"clinical_significance":[],"id":"rs1371602420","seq_region_name":"7","feature_type":"variation","strand":1,"end":140479629,"alleles":["T","G"],"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479629},{"seq_region_name":"7","id":"rs1215544567","clinical_significance":[],"strand":1,"feature_type":"variation","end":140479630,"alleles":["A","C","G"],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140479630,"source":"dbSNP"},{"alleles":["G","A"],"end":140479631,"feature_type":"variation","strand":1,"source":"dbSNP","start":140479631,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795234673"},{"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140479634,"source":"dbSNP","strand":1,"feature_type":"variation","end":140479634,"alleles":["T","C"],"seq_region_name":"7","id":"rs1795234718","clinical_significance":[]},{"seq_region_name":"7","id":"rs1251033447","clinical_significance":[],"start":140479635,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","end":140479635,"alleles":["C","A","G"],"strand":1,"feature_type":"variation"},{"id":"rs1276722184","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140479638,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140479638},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140479640,"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140479640,"source":"dbSNP","id":"rs764773817","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs984710032","seq_region_name":"7","consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479644,"feature_type":"variation","strand":1,"end":140479644,"alleles":["G","A"]},{"source":"dbSNP","start":140479646,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","end":140479646,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795234975","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140479647,"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140479647,"source":"dbSNP","seq_region_name":"7","id":"rs1795235006","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140479650,"alleles":["G","C"],"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479650,"clinical_significance":[],"seq_region_name":"7","id":"rs1177595690"},{"seq_region_name":"7","id":"rs909905392","clinical_significance":[],"alleles":["A","G"],"end":140479651,"strand":1,"feature_type":"variation","start":140479651,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant"},{"start":140479653,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","alleles":["A","G"],"end":140479653,"strand":1,"feature_type":"variation","id":"rs1421116354","seq_region_name":"7","clinical_significance":[]},{"end":140479654,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140479654,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795235247"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795235294","consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479656,"feature_type":"variation","strand":1,"end":140479656,"alleles":["C","A"]},{"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479658,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140479658,"clinical_significance":[],"seq_region_name":"7","id":"rs932536313"},{"alleles":["T","C"],"end":140479659,"feature_type":"variation","strand":1,"source":"dbSNP","start":140479659,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1435925043"},{"seq_region_name":"7","id":"rs1795235448","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["TAGTTAG","TAG"],"end":140479665,"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140479659,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140479660,"alleles":["A","G"],"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479660,"clinical_significance":[],"seq_region_name":"7","id":"rs1758870344"},{"seq_region_name":"7","id":"rs2130389135","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140479665,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140479665},{"strand":1,"feature_type":"variation","end":140479666,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140479666,"source":"dbSNP","seq_region_name":"7","id":"rs1427817385","clinical_significance":[]},{"seq_region_name":"7","id":"rs985379095","clinical_significance":[],"end":140479669,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140479669,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140479674,"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140479674,"source":"dbSNP","seq_region_name":"7","id":"rs1476721789","clinical_significance":[]},{"end":140479675,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140479675,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795235659"},{"end":140479676,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140479676,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","seq_region_name":"7","id":"rs1795235707","clinical_significance":[]},{"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479677,"feature_type":"variation","strand":1,"end":140479677,"alleles":["C","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs181420735"},{"start":140479680,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","alleles":["G","A","C"],"end":140479680,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795235837","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795235880","end":140479682,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140479682,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs941335046","clinical_significance":[],"end":140479686,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140479686,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant"},{"id":"rs925973781","seq_region_name":"7","clinical_significance":[],"start":140479687,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","alleles":["C","G","T"],"end":140479687,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1354108007","clinical_significance":[],"start":140479688,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","end":140479688,"alleles":["T","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs750133287","clinical_significance":[],"start":140479689,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","alleles":["G","C"],"end":140479689,"strand":1,"feature_type":"variation"},{"end":140479690,"alleles":["A","G","T"],"strand":1,"feature_type":"variation","start":140479690,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","id":"rs1194006637","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","C"],"end":140479693,"feature_type":"variation","strand":1,"source":"dbSNP","start":140479693,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1037532528"},{"alleles":["A","G"],"end":140479694,"strand":1,"feature_type":"variation","start":140479694,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","seq_region_name":"7","id":"rs935982141","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1462010180","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140479695,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479695},{"clinical_significance":[],"seq_region_name":"7","id":"rs1215576189","end":140479696,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140479696,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140479704,"alleles":["TGGAGCTGG","TGG"],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140479696,"source":"dbSNP","seq_region_name":"7","id":"rs1795236401","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140479697,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479697,"clinical_significance":[],"seq_region_name":"7","id":"rs1328569922"},{"seq_region_name":"7","id":"rs1585508197","clinical_significance":[],"strand":1,"feature_type":"variation","end":140479699,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140479699,"source":"dbSNP"},{"source":"dbSNP","start":140479700,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","end":140479700,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs7811509"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795236733","source":"dbSNP","start":140479701,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","end":140479701,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130389332","source":"dbSNP","start":140479704,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140479704,"feature_type":"variation","strand":1},{"end":140479705,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140479705,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","id":"rs1795236790","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140479710,"alleles":["G","A"],"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479710,"clinical_significance":[],"seq_region_name":"7","id":"rs1280579038"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130389351","end":140479711,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140479711,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs372393787","end":140479712,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140479712,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1585508232","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140479713,"source":"dbSNP","strand":1,"feature_type":"variation","end":140479713,"alleles":["A","G"]},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140479714,"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140479714,"source":"dbSNP","seq_region_name":"7","id":"rs539927901","clinical_significance":[]},{"clinical_significance":[],"id":"rs889939817","seq_region_name":"7","end":140479721,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140479721,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38"},{"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479729,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140479729,"clinical_significance":[],"seq_region_name":"7","id":"rs1007588583"},{"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479734,"feature_type":"variation","strand":1,"end":140479734,"alleles":["G","A"],"clinical_significance":[],"id":"rs1795237147","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795237188","clinical_significance":[],"start":140479737,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","end":140479737,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140479740,"alleles":["G","A"],"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479740,"clinical_significance":[],"id":"rs1795237234","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795237301","clinical_significance":[],"strand":1,"feature_type":"variation","end":140479741,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140479741,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140479742,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479742,"clinical_significance":[],"seq_region_name":"7","id":"rs1585508263"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1043980088","source":"dbSNP","start":140479743,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140479743,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140479745,"source":"dbSNP","strand":1,"feature_type":"variation","end":140479745,"alleles":["G","C"],"seq_region_name":"7","id":"rs1795237474","clinical_significance":[]},{"seq_region_name":"7","id":"rs1221780273","clinical_significance":[],"start":140479749,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","end":140479749,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140479752,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479752,"clinical_significance":[],"seq_region_name":"7","id":"rs1795237589"},{"start":140479753,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","end":140479753,"alleles":["A","G"],"strand":1,"feature_type":"variation","id":"rs1046291107","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140479754,"source":"dbSNP","strand":1,"feature_type":"variation","end":140479754,"alleles":["C","T"],"seq_region_name":"7","id":"rs903519239","clinical_significance":[]},{"clinical_significance":[],"id":"rs1415726910","seq_region_name":"7","source":"dbSNP","start":140479758,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140479758,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140479759,"alleles":["C","A","T"],"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479759,"clinical_significance":[],"id":"rs1795237834","seq_region_name":"7"},{"start":140479761,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","alleles":["A","G"],"end":140479761,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795237886","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795237926","clinical_significance":[],"start":140479762,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","end":140479764,"alleles":["TTT","TT"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs906011706","seq_region_name":"7","consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479769,"feature_type":"variation","strand":1,"end":140479769,"alleles":["A","G"]},{"feature_type":"variation","strand":1,"end":140479773,"alleles":["A","C"],"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479773,"clinical_significance":[],"id":"rs1795238048","seq_region_name":"7"},{"end":140479776,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140479776,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","id":"rs1002222166","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","C"],"end":140479779,"strand":1,"feature_type":"variation","start":140479779,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","seq_region_name":"7","id":"rs1795238164","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140479782,"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140479782,"source":"dbSNP","id":"rs1049293134","seq_region_name":"7","clinical_significance":[]},{"id":"rs1795238279","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140479783,"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140479783,"source":"dbSNP"},{"alleles":["G","A","T"],"end":140479785,"strand":1,"feature_type":"variation","start":140479785,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","id":"rs1377969983","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795238397","clinical_significance":[],"strand":1,"feature_type":"variation","end":140479786,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140479786,"source":"dbSNP"},{"alleles":["A","G"],"end":140479788,"strand":1,"feature_type":"variation","start":140479788,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","seq_region_name":"7","id":"rs1795238449","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795238491","source":"dbSNP","start":140479789,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","end":140479789,"alleles":["C","T"],"feature_type":"variation","strand":1},{"start":140479792,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","alleles":["G","A"],"end":140479792,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs535775203","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140479794,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479794,"clinical_significance":[],"seq_region_name":"7","id":"rs1795238640"},{"start":140479794,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","end":140479800,"alleles":["TCTATCT","TCT"],"strand":1,"feature_type":"variation","id":"rs1795238685","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479797,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140479797,"clinical_significance":[],"seq_region_name":"7","id":"rs1031181320"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1015303557","source":"dbSNP","start":140479798,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","end":140479798,"alleles":["T","A","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1192688341","seq_region_name":"7","consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479799,"feature_type":"variation","strand":1,"end":140479799,"alleles":["C","G"]},{"seq_region_name":"7","id":"rs377186120","clinical_significance":[],"start":140479801,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","alleles":["G","A"],"end":140479801,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140479803,"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140479803,"source":"dbSNP","seq_region_name":"7","id":"rs752003244","clinical_significance":[]},{"seq_region_name":"7","id":"rs1238988077","clinical_significance":[],"start":140479808,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","end":140479808,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs868334772","clinical_significance":[],"strand":1,"feature_type":"variation","end":140479819,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140479819,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1013322294","clinical_significance":[],"start":140479820,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","end":140479820,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1029935250","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140479828,"source":"dbSNP","strand":1,"feature_type":"variation","end":140479828,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795239294","feature_type":"variation","strand":1,"end":140479829,"alleles":["A","G","T"],"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479829},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795239372","alleles":["G","A"],"end":140479831,"feature_type":"variation","strand":1,"source":"dbSNP","start":140479831,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795239429","clinical_significance":[],"end":140479834,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140479834,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant"},{"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479837,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140479837,"clinical_significance":[],"seq_region_name":"7","id":"rs1795239484"},{"strand":1,"feature_type":"variation","end":140479838,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140479838,"source":"dbSNP","id":"rs550549681","seq_region_name":"7","clinical_significance":[]},{"start":140479841,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","alleles":["G","C"],"end":140479841,"strand":1,"feature_type":"variation","id":"rs1467991418","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140479843,"source":"dbSNP","strand":1,"feature_type":"variation","end":140479843,"alleles":["C","T"],"id":"rs1795239637","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs748855724","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140479844,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479844},{"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140479847,"source":"dbSNP","strand":1,"feature_type":"variation","end":140479847,"alleles":["C","T"],"id":"rs969200056","seq_region_name":"7","clinical_significance":[]},{"start":140479850,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","end":140479850,"alleles":["A","G"],"strand":1,"feature_type":"variation","id":"rs2130389790","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs985411331","source":"dbSNP","start":140479851,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","end":140479851,"alleles":["T","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs562477836","source":"dbSNP","start":140479852,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","end":140479852,"alleles":["G","C"],"feature_type":"variation","strand":1},{"alleles":["G","T"],"end":140479853,"feature_type":"variation","strand":1,"source":"dbSNP","start":140479853,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585508417"},{"alleles":["T","G"],"end":140479855,"feature_type":"variation","strand":1,"source":"dbSNP","start":140479855,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795239992"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1316318488","end":140479857,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140479857,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140479864,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140479864,"source":"dbSNP","seq_region_name":"7","id":"rs1277737316","clinical_significance":[]},{"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479868,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140479868,"clinical_significance":[],"id":"rs1234466023","seq_region_name":"7"},{"clinical_significance":[],"id":"rs985118241","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140479871,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479871},{"start":140479872,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","end":140479872,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs781581950","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140479875,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140479875,"source":"dbSNP","seq_region_name":"7","id":"rs1795240290","clinical_significance":[]},{"id":"rs925860550","seq_region_name":"7","clinical_significance":[],"end":140479876,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140479876,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant"},{"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140479877,"source":"dbSNP","strand":1,"feature_type":"variation","end":140479877,"alleles":["C","T"],"seq_region_name":"7","id":"rs1381879671","clinical_significance":[]},{"end":140479878,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140479878,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1301438898"},{"clinical_significance":[],"id":"rs1447995483","seq_region_name":"7","feature_type":"variation","strand":1,"end":140479879,"alleles":["T","C"],"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479879},{"seq_region_name":"7","id":"rs1795240499","clinical_significance":[],"start":140479887,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","end":140479887,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"alleles":["A","C"],"end":140479892,"feature_type":"variation","strand":1,"source":"dbSNP","start":140479892,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1355584883"},{"end":140479893,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140479893,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795240594"},{"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140479894,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140479894,"seq_region_name":"7","id":"rs138808638","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs957360443","feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140479897,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479897},{"alleles":["G","C"],"end":140479898,"strand":1,"feature_type":"variation","start":140479898,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","id":"rs768521834","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140479902,"alleles":["C","G"],"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479902,"clinical_significance":[],"seq_region_name":"7","id":"rs972736365"},{"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479904,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140479904,"clinical_significance":[],"seq_region_name":"7","id":"rs1475636742"},{"seq_region_name":"7","id":"rs1169607098","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140479907,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140479907},{"seq_region_name":"7","id":"rs918570936","clinical_significance":[],"start":140479909,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","end":140479909,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1415749876","clinical_significance":[],"strand":1,"feature_type":"variation","end":140479912,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140479912,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1179866782","clinical_significance":[],"start":140479918,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","end":140479922,"alleles":["ACTTA","A"],"strand":1,"feature_type":"variation"},{"id":"rs1472442654","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140479921,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TAATAA","TAA"],"end":140479926},{"clinical_significance":[],"id":"rs1795241224","seq_region_name":"7","feature_type":"variation","strand":1,"end":140479923,"alleles":["A","G"],"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479923},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795241283","source":"dbSNP","start":140479924,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","end":140479924,"alleles":["T","A"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140479926,"source":"dbSNP","strand":1,"feature_type":"variation","end":140479932,"alleles":["AAGGTTA","A"],"seq_region_name":"7","id":"rs1238659301","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140479932,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140479932,"source":"dbSNP","seq_region_name":"7","id":"rs934107028","clinical_significance":[]},{"start":140479934,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","end":140479934,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs1795241460","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","G","T"],"end":140479937,"feature_type":"variation","strand":1,"source":"dbSNP","start":140479937,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1456446603"},{"end":140479945,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140479945,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs116802650"},{"start":140479946,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","end":140479946,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs911429740","clinical_significance":[]},{"alleles":["C","G"],"end":140479948,"feature_type":"variation","strand":1,"source":"dbSNP","start":140479948,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1222660785"},{"strand":1,"feature_type":"variation","end":140479953,"alleles":["AGAGA","AGA"],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140479949,"source":"dbSNP","id":"rs1323698887","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479953,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140479953,"clinical_significance":[],"id":"rs1330140627","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585508586","source":"dbSNP","start":140479958,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","end":140479958,"alleles":["A","G","T"],"feature_type":"variation","strand":1},{"alleles":["T","A"],"end":140479959,"feature_type":"variation","strand":1,"source":"dbSNP","start":140479959,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1311067670"},{"seq_region_name":"7","id":"rs2130390105","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140479960,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140479960},{"clinical_significance":[],"seq_region_name":"7","id":"rs1356698570","feature_type":"variation","strand":1,"end":140479962,"alleles":["TT","TTT"],"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479961},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795242081","end":140479962,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140479962,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1228056632","seq_region_name":"7","feature_type":"variation","strand":1,"end":140479972,"alleles":["GCCAAGTAT","-"],"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479964},{"clinical_significance":[],"seq_region_name":"7","id":"rs566529973","consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479967,"feature_type":"variation","strand":1,"end":140479967,"alleles":["A","G"]},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140479973,"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140479973,"source":"dbSNP","id":"rs1378307748","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795242251","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140479977,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140479977},{"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140479982,"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140479982,"source":"dbSNP","seq_region_name":"7","id":"rs942844281","clinical_significance":[]},{"alleles":["C","G"],"end":140479983,"strand":1,"feature_type":"variation","start":140479983,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","seq_region_name":"7","id":"rs1795242356","clinical_significance":[]},{"end":140479985,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140479985,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","seq_region_name":"7","id":"rs1044377214","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795242435","end":140479990,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140479990,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140479992,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140479992,"seq_region_name":"7","id":"rs1795242476","clinical_significance":[]},{"alleles":["G","A"],"end":140479993,"feature_type":"variation","strand":1,"source":"dbSNP","start":140479993,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795242517"},{"clinical_significance":[],"seq_region_name":"7","id":"rs753338916","feature_type":"variation","strand":1,"alleles":["GGG","GG"],"end":140479997,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140479995},{"alleles":["G","T"],"end":140479997,"feature_type":"variation","strand":1,"source":"dbSNP","start":140479997,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1297079323"},{"seq_region_name":"7","id":"rs2130390238","clinical_significance":[],"start":140480000,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","T"],"end":140480000,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs748432759","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480003,"feature_type":"variation","strand":1,"end":140480003,"alleles":["C","G"]},{"start":140480004,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","G"],"end":140480004,"strand":1,"feature_type":"variation","id":"rs1795242698","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140480008,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480008,"clinical_significance":[],"id":"rs935009453","seq_region_name":"7"},{"source":"dbSNP","start":140480010,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140480010,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs950155753"},{"seq_region_name":"7","id":"rs1795242839","clinical_significance":[],"start":140480010,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","-"],"end":140480010,"strand":1,"feature_type":"variation"},{"alleles":["C","T"],"end":140480013,"strand":1,"feature_type":"variation","start":140480013,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1052122006","clinical_significance":[]},{"id":"rs28756184","seq_region_name":"7","clinical_significance":[],"start":140480018,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140480018,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs2130390299","clinical_significance":[],"start":140480021,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140480021,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs937521089","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140480025,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480025},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140480027,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480027,"source":"dbSNP","seq_region_name":"7","id":"rs1380849689","clinical_significance":[]},{"seq_region_name":"7","id":"rs1049303214","clinical_significance":[],"strand":1,"feature_type":"variation","end":140480029,"alleles":["A","C","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480029,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140480034,"alleles":["A","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480034,"clinical_significance":[],"seq_region_name":"7","id":"rs1795243677"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480035,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140480035,"clinical_significance":[],"seq_region_name":"7","id":"rs1437735307"},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140480037,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480037,"clinical_significance":[],"seq_region_name":"7","id":"rs2130390346"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1237690325","source":"dbSNP","start":140480038,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140480038,"feature_type":"variation","strand":1},{"end":140480039,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140480039,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795243921"},{"seq_region_name":"7","id":"rs1585508717","clinical_significance":[],"start":140480042,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140480042,"strand":1,"feature_type":"variation"},{"start":140480043,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","A","T"],"end":140480043,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1191802838","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140480055,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480055,"source":"dbSNP","seq_region_name":"7","id":"rs1489600977","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480058,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140480058,"clinical_significance":[],"seq_region_name":"7","id":"rs1013372975"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1263844049","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480061,"feature_type":"variation","strand":1,"end":140480061,"alleles":["T","G"]},{"clinical_significance":[],"id":"rs1023384978","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480066,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140480066},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480071,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140480071,"clinical_significance":[],"seq_region_name":"7","id":"rs2130390423"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1234687267","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480072,"feature_type":"variation","strand":1,"end":140480073,"alleles":["CT","CTCT"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs905037915","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480075,"feature_type":"variation","strand":1,"end":140480075,"alleles":["C","A"]},{"seq_region_name":"7","id":"rs1288580265","clinical_significance":[],"start":140480081,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","G","T"],"end":140480081,"strand":1,"feature_type":"variation"},{"id":"rs1006026687","seq_region_name":"7","clinical_significance":[],"end":140480084,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140480084,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs77774226","clinical_significance":[],"start":140480097,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140480097,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1036631275","end":140480112,"alleles":["AATAATAATAATAATA","AATAATAATAATA","AATAATAATAATAATAATA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140480097,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480100,"feature_type":"variation","strand":1,"alleles":["AATAA","A"],"end":140480104,"clinical_significance":[],"seq_region_name":"7","id":"rs1369305560"},{"start":140480107,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140480108,"alleles":["AT","ATCAT"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1215153244","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480113,"source":"dbSNP","strand":1,"feature_type":"variation","end":140480113,"alleles":["G","A","T"],"id":"rs1403949873","seq_region_name":"7","clinical_significance":[]},{"end":140480115,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140480115,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130390546"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480119,"source":"dbSNP","strand":1,"feature_type":"variation","end":140480119,"alleles":["G","T"],"seq_region_name":"7","id":"rs2130390548","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480123,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140480123,"id":"rs1795245136","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795245186","seq_region_name":"7","feature_type":"variation","strand":1,"end":140480124,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480124},{"end":140480126,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140480126,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1275002785","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140480131,"alleles":["A","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480131,"clinical_significance":[],"seq_region_name":"7","id":"rs1795245297"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140480132,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480132,"source":"dbSNP","seq_region_name":"7","id":"rs1795245339","clinical_significance":[]},{"end":140480132,"alleles":["C","CC"],"strand":1,"feature_type":"variation","start":140480132,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1795245383","clinical_significance":[]},{"seq_region_name":"7","id":"rs998373525","clinical_significance":[],"start":140480133,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","T"],"end":140480133,"strand":1,"feature_type":"variation"},{"alleles":["T","C"],"end":140480136,"feature_type":"variation","strand":1,"source":"dbSNP","start":140480136,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795245506","seq_region_name":"7"},{"id":"rs1363109240","seq_region_name":"7","clinical_significance":[],"start":140480139,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140480139,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140480140,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480140,"source":"dbSNP","id":"rs1176898386","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1203600794","source":"dbSNP","start":140480141,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140480141,"alleles":["T","A"],"feature_type":"variation","strand":1},{"start":140480142,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","G"],"end":140480142,"strand":1,"feature_type":"variation","id":"rs1795245718","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480143,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140480143,"seq_region_name":"7","id":"rs1265350180","clinical_significance":[]},{"seq_region_name":"7","id":"rs570969070","clinical_significance":[],"end":140480149,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140480149,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"id":"rs1795245872","seq_region_name":"7","feature_type":"variation","strand":1,"end":140480150,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480150},{"seq_region_name":"7","id":"rs537954966","clinical_significance":[],"end":140480151,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140480151,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795245974","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480152,"feature_type":"variation","strand":1,"end":140480152,"alleles":["T","C"]},{"start":140480160,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140480160,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1257908137","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140480163,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480163,"clinical_significance":[],"seq_region_name":"7","id":"rs777848821"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1486128260","end":140480165,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140480165,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1190246269","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480166,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140480166},{"clinical_significance":[],"seq_region_name":"7","id":"rs972379260","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480167,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140480167},{"seq_region_name":"7","id":"rs954056579","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480168,"source":"dbSNP","strand":1,"feature_type":"variation","end":140480168,"alleles":["G","A","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1255578426","feature_type":"variation","strand":1,"end":140480169,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480169},{"seq_region_name":"7","id":"rs1472501577","clinical_significance":[],"alleles":["A","G"],"end":140480171,"strand":1,"feature_type":"variation","start":140480171,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"alleles":["A","T"],"end":140480172,"feature_type":"variation","strand":1,"source":"dbSNP","start":140480172,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795246471"},{"alleles":["A","C"],"end":140480175,"feature_type":"variation","strand":1,"source":"dbSNP","start":140480175,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795246521"},{"end":140480177,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140480177,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1025634731"},{"start":140480178,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140480178,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795246625","clinical_significance":[]},{"seq_region_name":"7","id":"rs1169044815","clinical_significance":[],"end":140480179,"alleles":["TG","-"],"strand":1,"feature_type":"variation","start":140480178,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"end":140480179,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140480179,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1795246693","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480180,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140480180,"seq_region_name":"7","id":"rs749593147","clinical_significance":[]},{"end":140480182,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140480182,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795246818"},{"seq_region_name":"7","id":"rs1257043480","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140480183,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480183,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130390814","end":140480186,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140480186,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"end":140480187,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140480187,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs986849832"},{"feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140480188,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480188,"clinical_significance":[],"seq_region_name":"7","id":"rs1408668242"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480190,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140480190,"seq_region_name":"7","id":"rs2130390851","clinical_significance":[]},{"source":"dbSNP","start":140480192,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140480192,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1313510260","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480193,"source":"dbSNP","strand":1,"feature_type":"variation","end":140480193,"alleles":["G","C"],"seq_region_name":"7","id":"rs1795247159","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1032937032","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480195,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140480195},{"seq_region_name":"7","id":"rs200041673","clinical_significance":[],"strand":1,"feature_type":"variation","end":140480197,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480197,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130390916","end":140480200,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140480200,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs957246922","clinical_significance":[],"alleles":["C","A","T"],"end":140480202,"strand":1,"feature_type":"variation","start":140480202,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"start":140480204,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140480204,"strand":1,"feature_type":"variation","id":"rs988831017","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795247493","feature_type":"variation","strand":1,"end":140480205,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480205},{"seq_region_name":"7","id":"rs1795247536","clinical_significance":[],"start":140480206,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140480206,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"start":140480210,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140480210,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1299830821","clinical_significance":[]},{"source":"dbSNP","start":140480211,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140480211,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795247623"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795247680","alleles":["T","C"],"end":140480215,"feature_type":"variation","strand":1,"source":"dbSNP","start":140480215,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795247727","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480220,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140480220},{"id":"rs911271816","seq_region_name":"7","clinical_significance":[],"start":140480223,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140480223,"alleles":["C","A","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs942874861","end":140480224,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140480224,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"alleles":["T","C"],"end":140480228,"feature_type":"variation","strand":1,"source":"dbSNP","start":140480228,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1339421525"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480231,"source":"dbSNP","strand":1,"feature_type":"variation","end":140480231,"alleles":["C","T"],"seq_region_name":"7","id":"rs1795247953","clinical_significance":[]},{"source":"dbSNP","start":140480238,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140480238,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795247991"},{"end":140480243,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140480243,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795248041"},{"seq_region_name":"7","id":"rs186883828","clinical_significance":[],"strand":1,"feature_type":"variation","end":140480245,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480245,"source":"dbSNP"},{"end":140480247,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140480247,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1430786908","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140480250,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480250,"source":"dbSNP","seq_region_name":"7","id":"rs1175757329","clinical_significance":[]},{"seq_region_name":"7","id":"rs1271393712","clinical_significance":[],"alleles":["C","T"],"end":140480251,"strand":1,"feature_type":"variation","start":140480251,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480252,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140480252,"id":"rs771072221","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs979600155","clinical_significance":[],"alleles":["G","A"],"end":140480253,"strand":1,"feature_type":"variation","start":140480253,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1425995209","clinical_significance":[],"start":140480254,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140480254,"alleles":["G","A","C"],"strand":1,"feature_type":"variation"},{"id":"rs2130391104","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140480255,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480255,"source":"dbSNP"},{"alleles":["G","A"],"end":140480256,"feature_type":"variation","strand":1,"source":"dbSNP","start":140480256,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs925423257"},{"feature_type":"variation","strand":1,"end":140480262,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480262,"clinical_significance":[],"seq_region_name":"7","id":"rs1585509062"},{"seq_region_name":"7","id":"rs1337396771","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140480264,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480264,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1488131207","clinical_significance":[],"end":140480266,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140480266,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480270,"feature_type":"variation","strand":1,"end":140480270,"alleles":["C","T"],"clinical_significance":[],"id":"rs1795248703","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1257298035","feature_type":"variation","strand":1,"end":140480271,"alleles":["A","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480271},{"id":"rs2130391142","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140480273,"strand":1,"feature_type":"variation","start":140480273,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"id":"rs1795248800","seq_region_name":"7","alleles":["ACTCA","A"],"end":140480279,"feature_type":"variation","strand":1,"source":"dbSNP","start":140480275,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480276,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140480276,"clinical_significance":[],"seq_region_name":"7","id":"rs1795248847"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480278,"source":"dbSNP","strand":1,"feature_type":"variation","end":140480278,"alleles":["C","T"],"seq_region_name":"7","id":"rs1795248890","clinical_significance":[]},{"seq_region_name":"7","id":"rs935623559","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140480279,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480279,"source":"dbSNP"},{"start":140480287,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140480287,"alleles":["G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1202767686","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140480291,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480291,"clinical_significance":[],"seq_region_name":"7","id":"rs1213859449"},{"seq_region_name":"7","id":"rs2130391193","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["-","T"],"end":140480293,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480294,"source":"dbSNP"},{"id":"rs1482550372","seq_region_name":"7","clinical_significance":[],"end":140480294,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140480294,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"id":"rs2130391202","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["AA","-"],"end":140480298,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480297},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480298,"feature_type":"variation","strand":1,"end":140480298,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795249616"},{"alleles":["T","C"],"end":140480299,"feature_type":"variation","strand":1,"source":"dbSNP","start":140480299,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1253779511","seq_region_name":"7"},{"seq_region_name":"7","id":"rs2130391221","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["TTCCTT","TT"],"end":140480304,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480299,"source":"dbSNP"},{"end":140480301,"alleles":["-","ACAAGGAGG"],"strand":1,"feature_type":"variation","start":140480302,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs2130391227","clinical_significance":[]},{"alleles":["A","C","G"],"end":140480307,"strand":1,"feature_type":"variation","start":140480307,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1585509111","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1222321822","seq_region_name":"7","alleles":["C","G","T"],"end":140480309,"feature_type":"variation","strand":1,"source":"dbSNP","start":140480309,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140480310,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480310,"clinical_significance":[],"seq_region_name":"7","id":"rs1795249826"},{"start":140480311,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140480311,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1280784572","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585509126","clinical_significance":[],"alleles":["G","A"],"end":140480318,"strand":1,"feature_type":"variation","start":140480318,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480319,"source":"dbSNP","strand":1,"feature_type":"variation","end":140480319,"alleles":["G","A","C"],"seq_region_name":"7","id":"rs1349773171","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140480321,"alleles":["G","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480321,"clinical_significance":[],"id":"rs1213358030","seq_region_name":"7"},{"end":140480322,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140480322,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1278430451"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1441955643","source":"dbSNP","start":140480323,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140480323,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795250263","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480327,"feature_type":"variation","strand":1,"end":140480327,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs2130391328","clinical_significance":[],"start":140480328,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","C"],"end":140480328,"strand":1,"feature_type":"variation"},{"id":"rs1795250309","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140480332,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480332,"source":"dbSNP"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480333,"feature_type":"variation","strand":1,"end":140480333,"alleles":["C","A"],"clinical_significance":[],"id":"rs1795250361","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795250403","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480340,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140480340},{"id":"rs1795250450","seq_region_name":"7","clinical_significance":[],"end":140480341,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140480341,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1795250499","clinical_significance":[],"start":140480342,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140480342,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1194029823","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480343,"feature_type":"variation","strand":1,"end":140480347,"alleles":["GCCAC","GCCACCGCACTCCAGCCAC","GCCACCGCACTCTAGCCAC"]},{"alleles":["T","A","C"],"end":140480348,"strand":1,"feature_type":"variation","start":140480348,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1243866813","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140480349,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480349,"clinical_significance":[],"seq_region_name":"7","id":"rs1474717067"},{"feature_type":"variation","strand":1,"end":140480351,"alleles":["A","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480351,"clinical_significance":[],"seq_region_name":"7","id":"rs1795250787"},{"clinical_significance":[],"id":"rs1188483852","seq_region_name":"7","source":"dbSNP","start":140480353,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140480353,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480354,"source":"dbSNP","strand":1,"feature_type":"variation","end":140480354,"alleles":["C","G"],"seq_region_name":"7","id":"rs2130391442","clinical_significance":[]},{"alleles":["C","A","T"],"end":140480355,"feature_type":"variation","strand":1,"source":"dbSNP","start":140480355,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1396127214","seq_region_name":"7"},{"alleles":["G","A"],"end":140480363,"feature_type":"variation","strand":1,"source":"dbSNP","start":140480363,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs2130391462","seq_region_name":"7"},{"start":140480364,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140480364,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1171412004","clinical_significance":[]},{"seq_region_name":"7","id":"rs1052677766","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480372,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140480372},{"end":140480376,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140480376,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795251118","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["T","A","C","G"],"end":140480377,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480377,"source":"dbSNP","seq_region_name":"7","id":"rs10808045","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480379,"source":"dbSNP","strand":1,"feature_type":"variation","end":140480379,"alleles":["C","G"],"seq_region_name":"7","id":"rs1168889404","clinical_significance":[]},{"seq_region_name":"7","id":"rs1475202155","clinical_significance":[],"alleles":["C","G","T"],"end":140480380,"strand":1,"feature_type":"variation","start":140480380,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"alleles":["G","A"],"end":140480381,"feature_type":"variation","strand":1,"source":"dbSNP","start":140480381,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1369458289"},{"strand":1,"feature_type":"variation","end":140480382,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480382,"source":"dbSNP","seq_region_name":"7","id":"rs1795251588","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480383,"feature_type":"variation","strand":1,"end":140480383,"alleles":["C","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795251648"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480388,"feature_type":"variation","strand":1,"alleles":["AATAATAATAATA","AATAATAATA"],"end":140480400,"clinical_significance":[],"seq_region_name":"7","id":"rs1190014724"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795251753","source":"dbSNP","start":140480390,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140480390,"alleles":["T","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs535721381","source":"dbSNP","start":140480391,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140480391,"feature_type":"variation","strand":1},{"start":140480391,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["AA","A"],"end":140480392,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795251905","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795251999","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480394,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140480394},{"id":"rs1554451991","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140480395,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480395,"source":"dbSNP"},{"id":"rs1218499027","seq_region_name":"7","clinical_significance":[],"start":140480396,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140480407,"alleles":["TAATAGTAATAG","TAATAG"],"strand":1,"feature_type":"variation"},{"alleles":["-","ATT"],"end":140480398,"strand":1,"feature_type":"variation","start":140480399,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs565035900","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480399,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140480399,"seq_region_name":"7","id":"rs1585509279","clinical_significance":[]},{"source":"dbSNP","start":140480401,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140480401,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795252715","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1202486476","clinical_significance":[],"alleles":["G","A","C"],"end":140480407,"strand":1,"feature_type":"variation","start":140480407,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"id":"rs1795252828","seq_region_name":"7","feature_type":"variation","strand":1,"end":140480411,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480411},{"clinical_significance":[],"id":"rs1457874391","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480414,"feature_type":"variation","strand":1,"end":140480414,"alleles":["G","A"]},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140480416,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480416,"source":"dbSNP","id":"rs937516633","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795252996","feature_type":"variation","strand":1,"end":140480418,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480418},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480423,"feature_type":"variation","strand":1,"end":140480423,"alleles":["T","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs554476930"},{"end":140480426,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140480426,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs984892661"},{"feature_type":"variation","strand":1,"end":140480433,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480433,"clinical_significance":[],"seq_region_name":"7","id":"rs1434364753"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140480437,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480437,"source":"dbSNP","seq_region_name":"7","id":"rs1246657896","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140480441,"alleles":["G","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480441,"clinical_significance":[],"seq_region_name":"7","id":"rs1795253250"},{"seq_region_name":"7","id":"rs1304045723","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140480442,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480442,"source":"dbSNP"},{"end":140480443,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140480443,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1338645791"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585509317","source":"dbSNP","start":140480445,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140480445,"alleles":["A","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795253481","end":140480447,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140480447,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"end":140480452,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140480452,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1795253542","clinical_significance":[]},{"seq_region_name":"7","id":"rs1372970656","clinical_significance":[],"start":140480467,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["TTT","TT"],"end":140480469,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs572538238","feature_type":"variation","strand":1,"end":140480469,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480469},{"seq_region_name":"7","id":"rs1795253732","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480470,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140480470},{"seq_region_name":"7","id":"rs10224232","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480471,"source":"dbSNP","strand":1,"feature_type":"variation","end":140480471,"alleles":["T","A","C","G"]},{"start":140480472,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140480472,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795253956","clinical_significance":[]},{"id":"rs1273987830","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480474,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140480474},{"clinical_significance":[],"id":"rs1447423386","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140480476,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480476},{"clinical_significance":[],"id":"rs1795254122","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480477,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140480477},{"end":140480478,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140480478,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1044851597","clinical_significance":[]},{"source":"dbSNP","start":140480479,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140480479,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795254234"},{"seq_region_name":"7","id":"rs1329372566","clinical_significance":[],"alleles":["G","A","T"],"end":140480481,"strand":1,"feature_type":"variation","start":140480481,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"start":140480482,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","A","T"],"end":140480482,"strand":1,"feature_type":"variation","id":"rs10952680","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140480483,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140480483,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1286514646","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140480484,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480484,"clinical_significance":[],"seq_region_name":"7","id":"rs1795254591"},{"alleles":["G","A"],"end":140480485,"strand":1,"feature_type":"variation","start":140480485,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1391674168","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1006365971","clinical_significance":[],"end":140480492,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140480492,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"end":140480494,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140480494,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1563101455"},{"alleles":["G","A","T"],"end":140480495,"strand":1,"feature_type":"variation","start":140480495,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1445341150","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480497,"source":"dbSNP","strand":1,"feature_type":"variation","end":140480497,"alleles":["C","T"],"seq_region_name":"7","id":"rs1208705410","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1456651707","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480504,"feature_type":"variation","strand":1,"end":140480504,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1384999065","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140480505,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480505},{"id":"rs1795255091","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480508,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140480508},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140480509,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480509,"source":"dbSNP","seq_region_name":"7","id":"rs1795255172","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795255251","feature_type":"variation","strand":1,"end":140480510,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480510},{"source":"dbSNP","start":140480512,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140480512,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1179879695"},{"feature_type":"variation","strand":1,"end":140480513,"alleles":["T","A","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480513,"clinical_significance":[],"seq_region_name":"7","id":"rs1795255411"},{"seq_region_name":"7","id":"rs1037570491","clinical_significance":[],"start":140480514,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140480514,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"id":"rs1795255625","seq_region_name":"7","clinical_significance":[],"start":140480515,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140480515,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480517,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140480517,"seq_region_name":"7","id":"rs1795255720","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480518,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","-"],"end":140480518,"id":"rs1455936159","seq_region_name":"7","clinical_significance":[]},{"end":140480519,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140480519,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1239505742","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480522,"feature_type":"variation","strand":1,"end":140480522,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs543805042"},{"id":"rs1436881839","seq_region_name":"7","clinical_significance":[],"start":140480523,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140480523,"alleles":["G","A","C"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140480524,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140480524,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs993414951"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480525,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140480525,"id":"rs933670749","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["GGGGGG","GGGGG"],"end":140480530,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480525,"source":"dbSNP","seq_region_name":"7","id":"rs1795256321","clinical_significance":[]},{"end":140480526,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140480526,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1377369625","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1470309956","source":"dbSNP","start":140480527,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140480527,"feature_type":"variation","strand":1},{"end":140480531,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140480531,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1476420870","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795256752","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140480532,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480532},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795256825","end":140480535,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140480535,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795256881","clinical_significance":[],"alleles":["C","T"],"end":140480536,"strand":1,"feature_type":"variation","start":140480536,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"strand":1,"feature_type":"variation","end":140480539,"alleles":["C","A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480539,"source":"dbSNP","seq_region_name":"7","id":"rs544337772","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480541,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140480541,"seq_region_name":"7","id":"rs1795257005","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140480542,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480542,"source":"dbSNP","id":"rs889510654","seq_region_name":"7","clinical_significance":[]},{"id":"rs1795257149","seq_region_name":"7","clinical_significance":[],"end":140480544,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140480544,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1563101503","clinical_significance":[],"strand":1,"feature_type":"variation","end":140480552,"alleles":["TT","TTT"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480551,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140480552,"alleles":["T","C","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480552,"source":"dbSNP","seq_region_name":"7","id":"rs1382210745","clinical_significance":[]},{"alleles":["G","C"],"end":140480553,"strand":1,"feature_type":"variation","start":140480553,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1795257297","seq_region_name":"7","clinical_significance":[]},{"end":140480559,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140480559,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795257346"},{"source":"dbSNP","start":140480560,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140480560,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795257398","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140480562,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480562,"clinical_significance":[],"id":"rs1385293492","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795257487","source":"dbSNP","start":140480563,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140480563,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs2130392206","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480564,"source":"dbSNP","strand":1,"feature_type":"variation","end":140480564,"alleles":["G","A"]},{"id":"rs1795257555","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140480567,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480567,"source":"dbSNP"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480572,"feature_type":"variation","strand":1,"end":140480572,"alleles":["C","T"],"clinical_significance":[],"id":"rs189882252","seq_region_name":"7"},{"end":140480574,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140480574,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs867253172"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480575,"source":"dbSNP","strand":1,"feature_type":"variation","end":140480575,"alleles":["T","G"],"seq_region_name":"7","id":"rs1008154213","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480579,"source":"dbSNP","strand":1,"feature_type":"variation","end":140480579,"alleles":["A","G"],"seq_region_name":"7","id":"rs1795257840","clinical_significance":[]},{"end":140480580,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140480580,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs2130392248","clinical_significance":[]},{"clinical_significance":[],"id":"rs1159594730","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480580,"feature_type":"variation","strand":1,"end":140480583,"alleles":["CCCC","CCCCC"]},{"end":140480581,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140480581,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs28648799"},{"clinical_significance":[],"id":"rs1378950340","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480582,"feature_type":"variation","strand":1,"end":140480582,"alleles":["C","A","G"]},{"end":140480583,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140480583,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1156322678","clinical_significance":[]},{"end":140480584,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140480584,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1585509558","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585509563","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140480589,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480589},{"id":"rs373336337","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140480593,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480593,"source":"dbSNP"},{"source":"dbSNP","start":140480593,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140480598,"alleles":["AAAAAA","AAAAA"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs570964832"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480595,"source":"dbSNP","strand":1,"feature_type":"variation","end":140480595,"alleles":["A","G"],"seq_region_name":"7","id":"rs560440817","clinical_significance":[]},{"end":140480599,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140480599,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1010190743"},{"clinical_significance":[],"id":"rs1795258714","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480600,"feature_type":"variation","strand":1,"end":140480600,"alleles":["A","G"]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480602,"feature_type":"variation","strand":1,"alleles":["AAAAAAA","AAAAAA","AAAAAAAA"],"end":140480608,"clinical_significance":[],"seq_region_name":"7","id":"rs1267970249"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480603,"source":"dbSNP","strand":1,"feature_type":"variation","end":140480603,"alleles":["A","G"],"seq_region_name":"7","id":"rs1795258855","clinical_significance":[]},{"seq_region_name":"7","id":"rs527493987","clinical_significance":[],"end":140480609,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140480609,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795258994","end":140480614,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140480614,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795259048","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480615,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140480615},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795259125","source":"dbSNP","start":140480617,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140480617,"alleles":["T","A","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs552303796","source":"dbSNP","start":140480618,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140480618,"alleles":["C","G","T"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140480619,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480619,"source":"dbSNP","seq_region_name":"7","id":"rs971806497","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140480620,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480620,"clinical_significance":[],"seq_region_name":"7","id":"rs979910778"},{"clinical_significance":[],"id":"rs2130392475","seq_region_name":"7","source":"dbSNP","start":140480621,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140480621,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795259481","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480622,"feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140480622},{"seq_region_name":"7","id":"rs1345873389","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480623,"source":"dbSNP","strand":1,"feature_type":"variation","end":140480623,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1795259585","clinical_significance":[],"strand":1,"feature_type":"variation","end":140480626,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480626,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1795259639","seq_region_name":"7","feature_type":"variation","strand":1,"end":140480628,"alleles":["G","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480628},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480629,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140480629,"clinical_significance":[],"seq_region_name":"7","id":"rs1795259689"},{"seq_region_name":"7","id":"rs1585509613","clinical_significance":[],"start":140480630,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140480630,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795259799","end":140480631,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140480631,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1276665180","clinical_significance":[],"start":140480632,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","G","T"],"end":140480632,"strand":1,"feature_type":"variation"},{"alleles":["C","T"],"end":140480633,"strand":1,"feature_type":"variation","start":140480633,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1231383921","clinical_significance":[]},{"clinical_significance":[],"id":"rs1336125872","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480634,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140480634},{"id":"rs925506918","seq_region_name":"7","clinical_significance":[],"end":140480637,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","start":140480637,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1795260137","clinical_significance":[],"alleles":["G","T"],"end":140480638,"strand":1,"feature_type":"variation","start":140480638,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"id":"rs1795260179","seq_region_name":"7","clinical_significance":[],"start":140480642,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140480642,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480643,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140480643,"seq_region_name":"7","id":"rs74527832","clinical_significance":[]},{"start":140480644,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140480644,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1318327160","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795260396","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480646,"feature_type":"variation","strand":1,"end":140480646,"alleles":["T","C"]},{"strand":1,"feature_type":"variation","end":140480648,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480648,"source":"dbSNP","seq_region_name":"7","id":"rs1795260437","clinical_significance":[]},{"end":140480651,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140480651,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585509661"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795260591","feature_type":"variation","strand":1,"alleles":["CGAGGCTGAGGCAGGAGAATG","-"],"end":140480671,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480651},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480652,"feature_type":"variation","strand":1,"end":140480652,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1415536043"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795260681","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140480654,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480654},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480660,"feature_type":"variation","strand":1,"end":140480660,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs958756994"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140480663,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480663,"source":"dbSNP","seq_region_name":"7","id":"rs988392327","clinical_significance":[]},{"alleles":["G","A"],"end":140480664,"strand":1,"feature_type":"variation","start":140480664,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1585509676","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140480666,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140480666,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585509681"},{"seq_region_name":"7","id":"rs918147993","clinical_significance":[],"strand":1,"feature_type":"variation","end":140480670,"alleles":["T","A","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480670,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480671,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140480671,"seq_region_name":"7","id":"rs1585509697","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140480672,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480672,"source":"dbSNP","seq_region_name":"7","id":"rs1479271045","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1428105816","source":"dbSNP","start":140480673,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140480673,"alleles":["A","C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1194135851","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140480674,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480674},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480675,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140480675,"seq_region_name":"7","id":"rs1585509717","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795261521","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480676,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140480676},{"feature_type":"variation","strand":1,"end":140480681,"alleles":["C","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480681,"clinical_significance":[],"seq_region_name":"7","id":"rs1795261572"},{"end":140480682,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140480682,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs565289417","clinical_significance":[]},{"source":"dbSNP","start":140480684,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140480684,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1327212751"},{"clinical_significance":[],"seq_region_name":"7","id":"rs909413070","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480687,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140480687},{"id":"rs2130392716","seq_region_name":"7","clinical_significance":[],"alleles":["C","G","T"],"end":140480688,"strand":1,"feature_type":"variation","start":140480688,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"alleles":["A","C","G"],"end":140480690,"strand":1,"feature_type":"variation","start":140480690,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs765189440","clinical_significance":[]},{"alleles":["A","G"],"end":140480691,"strand":1,"feature_type":"variation","start":140480691,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs2130392745","clinical_significance":[]},{"alleles":["C","G"],"end":140480693,"feature_type":"variation","strand":1,"source":"dbSNP","start":140480693,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1442899439","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["C","-"],"end":140480693,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480693,"clinical_significance":[],"seq_region_name":"7","id":"rs1795262017"},{"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140480694,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480694,"clinical_significance":[],"id":"rs1795262058","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1227902764","clinical_significance":[],"start":140480697,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140480697,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1795262195","clinical_significance":[],"alleles":["T","C"],"end":140480700,"strand":1,"feature_type":"variation","start":140480700,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140480701,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480701,"source":"dbSNP","seq_region_name":"7","id":"rs1795262252","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140480705,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480705,"clinical_significance":[],"seq_region_name":"7","id":"rs2130392792"},{"seq_region_name":"7","id":"rs1280862588","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480707,"source":"dbSNP","strand":1,"feature_type":"variation","end":140480707,"alleles":["A","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795262341","feature_type":"variation","strand":1,"end":140480708,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480708},{"clinical_significance":[],"seq_region_name":"7","id":"rs940856298","source":"dbSNP","start":140480711,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140480711,"alleles":["C","G","T"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480712,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140480712,"id":"rs2130392816","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480714,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140480714,"clinical_significance":[],"seq_region_name":"7","id":"rs1795262461"},{"seq_region_name":"7","id":"rs949053013","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140480717,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480717,"source":"dbSNP"},{"source":"dbSNP","start":140480718,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140480718,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795262567"},{"clinical_significance":[],"id":"rs540847165","seq_region_name":"7","feature_type":"variation","strand":1,"end":140480719,"alleles":["C","G","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480719},{"alleles":["C","T"],"end":140480721,"strand":1,"feature_type":"variation","start":140480721,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1208508734","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1267181755","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480722,"feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140480722},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480723,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140480723,"seq_region_name":"7","id":"rs1438736783","clinical_significance":[]},{"seq_region_name":"7","id":"rs926270431","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140480725,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480725,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs149536768","end":140480726,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140480726,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"id":"rs1795263030","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480727,"source":"dbSNP","strand":1,"feature_type":"variation","end":140480727,"alleles":["A","C"]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480730,"feature_type":"variation","strand":1,"end":140480730,"alleles":["C","T"],"clinical_significance":[],"id":"rs1037854409","seq_region_name":"7"},{"alleles":["T","C"],"end":140480733,"strand":1,"feature_type":"variation","start":140480733,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs897661290","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1472037379","source":"dbSNP","start":140480734,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140480734,"alleles":["G","A"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480735,"source":"dbSNP","strand":1,"feature_type":"variation","end":140480735,"alleles":["C","T"],"seq_region_name":"7","id":"rs1467721738","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1404715897","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480737,"feature_type":"variation","strand":1,"end":140480737,"alleles":["C","G","T"]},{"start":140480740,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140480740,"alleles":["C","A"],"strand":1,"feature_type":"variation","id":"rs1171020851","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1478584458","alleles":["C","T"],"end":140480744,"feature_type":"variation","strand":1,"source":"dbSNP","start":140480744,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480746,"feature_type":"variation","strand":1,"end":140480746,"alleles":["G","A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs115149391"},{"seq_region_name":"7","id":"rs1795263550","clinical_significance":[],"start":140480748,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140480748,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480750,"feature_type":"variation","strand":1,"alleles":["G","C","T"],"end":140480750,"clinical_significance":[],"seq_region_name":"7","id":"rs1051645290"},{"seq_region_name":"7","id":"rs1585509849","clinical_significance":[],"strand":1,"feature_type":"variation","end":140480752,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480752,"source":"dbSNP"},{"id":"rs1473096978","seq_region_name":"7","clinical_significance":[],"end":140480753,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","start":140480753,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"source":"dbSNP","start":140480759,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140480759,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1419315268"},{"alleles":["G","T"],"end":140480760,"feature_type":"variation","strand":1,"source":"dbSNP","start":140480760,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795263909","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1795263987","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480762,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140480762},{"id":"rs2130393016","seq_region_name":"7","clinical_significance":[],"alleles":["C","A"],"end":140480765,"strand":1,"feature_type":"variation","start":140480765,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1201853446","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480766,"source":"dbSNP","strand":1,"feature_type":"variation","end":140480766,"alleles":["A","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795264147","feature_type":"variation","strand":1,"end":140480767,"alleles":["T","A","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480767},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480768,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140480768,"seq_region_name":"7","id":"rs1795264244","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585509871","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480769,"feature_type":"variation","strand":1,"end":140480769,"alleles":["T","A","C","G"]},{"start":140480770,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["-","A","AA"],"end":140480769,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795264420","clinical_significance":[]},{"seq_region_name":"7","id":"rs1460984111","clinical_significance":[],"alleles":["C","A"],"end":140480770,"strand":1,"feature_type":"variation","start":140480770,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480771,"feature_type":"variation","strand":1,"end":140480782,"alleles":["AAAAAAAAAAAA","AAAAAAAAAA","AAAAAAAAAAA","AAAAAAAAAAAAA","AAAAAAAAAAAAAA","AAAAAAAAAAAAAAA"],"clinical_significance":[],"seq_region_name":"7","id":"rs34290301"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795264959","feature_type":"variation","strand":1,"alleles":["AAAAAAAAAAAACAAAAAGCAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAA"],"end":140480808,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480771},{"seq_region_name":"7","id":"rs1795265061","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480771,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AAAAAAAAAAAACAAAAAGCAAAAAAAAAAAAAAAAAAAC","AAAAAAAAAAAAC"],"end":140480810},{"seq_region_name":"7","id":"rs1795265168","clinical_significance":[],"strand":1,"feature_type":"variation","end":140480775,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480775,"source":"dbSNP"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480776,"feature_type":"variation","strand":1,"end":140480776,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795265252"},{"clinical_significance":[],"id":"rs1795265332","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480777,"feature_type":"variation","strand":1,"end":140480777,"alleles":["A","T"]},{"seq_region_name":"7","id":"rs1459811255","clinical_significance":[],"start":140480778,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140480777,"alleles":["-","G","T"],"strand":1,"feature_type":"variation"},{"id":"rs2130393124","seq_region_name":"7","clinical_significance":[],"end":140480778,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140480778,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795265561","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480779,"feature_type":"variation","strand":1,"alleles":["-","C"],"end":140480778},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480782,"source":"dbSNP","strand":1,"feature_type":"variation","end":140480782,"alleles":["A","C","G"],"seq_region_name":"7","id":"rs1783636441","clinical_significance":[]},{"seq_region_name":"7","id":"rs1793674190","clinical_significance":[],"strand":1,"feature_type":"variation","end":140480782,"alleles":["-","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480783,"source":"dbSNP"},{"end":140480783,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140480783,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs28424111","clinical_significance":[]},{"alleles":["C","-"],"end":140480783,"feature_type":"variation","strand":1,"source":"dbSNP","start":140480783,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1292859955","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["C","CC"],"end":140480783,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480783,"clinical_significance":[],"seq_region_name":"7","id":"rs1795265795"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480783,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CAAAAAGC","-"],"end":140480790,"id":"rs372789235","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1392888145","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140480784,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480784,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140480788,"alleles":["AAAAA","AAAA","AAAAAA"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480784,"clinical_significance":[],"seq_region_name":"7","id":"rs1795266132"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1381986348","source":"dbSNP","start":140480785,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140480785,"alleles":["A","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1585509950","clinical_significance":[],"start":140480787,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140480787,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140480788,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480788,"source":"dbSNP","id":"rs2130393214","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795266374","seq_region_name":"7","end":140480791,"alleles":["AGCA","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140480788,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1015308467","source":"dbSNP","start":140480789,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A","C","T"],"end":140480789,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795266602","alleles":["G","GG"],"end":140480789,"feature_type":"variation","strand":1,"source":"dbSNP","start":140480789,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795266676","feature_type":"variation","strand":1,"end":140480789,"alleles":["G","-"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480789},{"clinical_significance":[],"seq_region_name":"7","id":"rs145412338","feature_type":"variation","strand":1,"alleles":["GC","-"],"end":140480790,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480789},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480790,"feature_type":"variation","strand":1,"end":140480789,"alleles":["-","A","AA"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795266893"},{"feature_type":"variation","strand":1,"end":140480790,"alleles":["C","-"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480790,"clinical_significance":[],"id":"rs371180902","seq_region_name":"7"},{"start":140480790,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140480790,"alleles":["C","A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs961138218","clinical_significance":[]},{"alleles":["CA","-"],"end":140480791,"strand":1,"feature_type":"variation","start":140480790,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1795267121","clinical_significance":[]},{"id":"rs1795267190","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480790,"source":"dbSNP","strand":1,"feature_type":"variation","end":140480792,"alleles":["CAA","-"]},{"strand":1,"feature_type":"variation","end":140480793,"alleles":["CAAA","-"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480790,"source":"dbSNP","seq_region_name":"7","id":"rs1795267280","clinical_significance":[]},{"id":"rs1795267361","seq_region_name":"7","clinical_significance":[],"alleles":["-","CAAAAAA"],"end":140480790,"strand":1,"feature_type":"variation","start":140480791,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"alleles":["A","C","G","T"],"end":140480791,"strand":1,"feature_type":"variation","start":140480791,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1795267444","clinical_significance":[]},{"start":140480791,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140480809,"alleles":["AAAAAAAAAAAAAAAAAAA","AAAAAAAAA","AAAAAAAAAAAA","AAAAAAAAAAAAAA","AAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAAAAAAAAAA"],"strand":1,"feature_type":"variation","id":"rs375455729","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140480793,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140480793,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1409380092"},{"start":140480794,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140480794,"alleles":["A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795268678","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795268747","alleles":["A","G"],"end":140480799,"feature_type":"variation","strand":1,"source":"dbSNP","start":140480799,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1795268813","seq_region_name":"7","source":"dbSNP","start":140480801,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140480801,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1180546073","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480802,"feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140480802},{"source":"dbSNP","start":140480803,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140480802,"alleles":["-","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1238914029"},{"seq_region_name":"7","id":"rs1795269065","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480803,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140480803},{"alleles":["A","ACA"],"end":140480803,"feature_type":"variation","strand":1,"source":"dbSNP","start":140480803,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795269148"},{"seq_region_name":"7","id":"rs1479794517","clinical_significance":[],"start":140480804,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140480804,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs889558726","alleles":["A","C"],"end":140480805,"feature_type":"variation","strand":1,"source":"dbSNP","start":140480805,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140480806,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480806,"source":"dbSNP","seq_region_name":"7","id":"rs890348476","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130393505","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480807,"feature_type":"variation","strand":1,"end":140480806,"alleles":["-","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1007412741","feature_type":"variation","strand":1,"end":140480807,"alleles":["A","C","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480807},{"clinical_significance":[],"seq_region_name":"7","id":"rs1323937912","feature_type":"variation","strand":1,"end":140480810,"alleles":["AAAC","-"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480807},{"id":"rs1585510063","seq_region_name":"7","clinical_significance":[],"alleles":["A","C"],"end":140480808,"strand":1,"feature_type":"variation","start":140480808,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"alleles":["AAC","-"],"end":140480810,"feature_type":"variation","strand":1,"source":"dbSNP","start":140480808,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1245938718","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1355001206","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["AACCCCTTTGCATTGTGCTTTTCA","A"],"end":140480831,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480808,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1392563080","alleles":["A","C"],"end":140480809,"feature_type":"variation","strand":1,"source":"dbSNP","start":140480809,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["AC","-"],"end":140480810,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480809,"source":"dbSNP","id":"rs1309376737","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs868792070","feature_type":"variation","strand":1,"end":140480810,"alleles":["C","A","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480810},{"start":140480810,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["CCCC","CCC","CCCCC"],"end":140480813,"strand":1,"feature_type":"variation","id":"rs200125231","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","T"],"end":140480811,"feature_type":"variation","strand":1,"source":"dbSNP","start":140480811,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1436736955"},{"strand":1,"feature_type":"variation","end":140480812,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480812,"source":"dbSNP","seq_region_name":"7","id":"rs1265346817","clinical_significance":[]},{"start":140480813,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140480813,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795270521","clinical_significance":[]},{"seq_region_name":"7","id":"rs1161412025","clinical_significance":[],"alleles":["T","A","C"],"end":140480814,"strand":1,"feature_type":"variation","start":140480814,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"start":140480816,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","A"],"end":140480816,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1340543595","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1197959481","source":"dbSNP","start":140480817,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140480817,"alleles":["G","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1380788244","seq_region_name":"7","source":"dbSNP","start":140480819,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140480819,"alleles":["A","G"],"feature_type":"variation","strand":1},{"id":"rs2130393635","seq_region_name":"7","clinical_significance":[],"alleles":["G","T"],"end":140480822,"strand":1,"feature_type":"variation","start":140480822,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"start":140480824,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140480824,"alleles":["G","T"],"strand":1,"feature_type":"variation","id":"rs1250003322","seq_region_name":"7","clinical_significance":[]},{"end":140480825,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140480825,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs2130393652","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140480826,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480826,"source":"dbSNP","seq_region_name":"7","id":"rs1795271008","clinical_significance":[]},{"start":140480826,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140480829,"alleles":["TTTT","TTT"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1482531096","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795271210","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480830,"feature_type":"variation","strand":1,"alleles":["CACAC","CAC"],"end":140480834},{"seq_region_name":"7","id":"rs1795271277","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480836,"source":"dbSNP","strand":1,"feature_type":"variation","end":140480836,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1407344125","clinical_significance":[],"end":140480839,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140480839,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"end":140480840,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140480840,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1018304356"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480842,"feature_type":"variation","strand":1,"alleles":["AATA","AATAAATA"],"end":140480845,"clinical_significance":[],"seq_region_name":"7","id":"rs942451717"},{"clinical_significance":[],"id":"rs1795271610","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480846,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140480846},{"alleles":["T","C"],"end":140480851,"strand":1,"feature_type":"variation","start":140480851,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1267249353","clinical_significance":[]},{"end":140480852,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140480852,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795271761"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480858,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140480858,"id":"rs1795271846","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs964382030","clinical_significance":[],"start":140480859,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140480859,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1795272037","seq_region_name":"7","source":"dbSNP","start":140480860,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140480860,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1259078134","source":"dbSNP","start":140480862,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140480862,"alleles":["A","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs893013265","alleles":["A","G"],"end":140480864,"feature_type":"variation","strand":1,"source":"dbSNP","start":140480864,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"id":"rs556032945","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140480865,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480865,"source":"dbSNP"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480868,"feature_type":"variation","strand":1,"end":140480868,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795272412"},{"start":140480871,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","T"],"end":140480871,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1237512056","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795272538","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480873,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140480873},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480874,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140480874,"id":"rs1795272613","seq_region_name":"7","clinical_significance":[]},{"id":"rs1314679729","seq_region_name":"7","clinical_significance":[],"start":140480876,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140480876,"alleles":["T","C","G"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140480882,"alleles":["C","CC"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480882,"source":"dbSNP","seq_region_name":"7","id":"rs1795272773","clinical_significance":[]},{"start":140480883,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140480891,"alleles":["TTTTTTTTT","TTTTTTTT","TTTTTTTTTT"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs561295664","clinical_significance":[]},{"start":140480890,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140480890,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795272959","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs371376598","source":"dbSNP","start":140480891,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140480891,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1473927446","feature_type":"variation","strand":1,"end":140480892,"alleles":["A","C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480892},{"strand":1,"feature_type":"variation","end":140480893,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480893,"source":"dbSNP","seq_region_name":"7","id":"rs1164048559","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140480894,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480894,"source":"dbSNP","seq_region_name":"7","id":"rs1346966766","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1373605527","end":140480895,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140480895,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1032798735","clinical_significance":[],"alleles":["C","A","T"],"end":140480896,"strand":1,"feature_type":"variation","start":140480896,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480897,"source":"dbSNP","strand":1,"feature_type":"variation","end":140480897,"alleles":["G","A","T"],"id":"rs1165957057","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1369648933","alleles":["C","T"],"end":140480899,"feature_type":"variation","strand":1,"source":"dbSNP","start":140480899,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"end":140480906,"alleles":["AAAA","AAAAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140480903,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795273626"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480905,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140480905,"clinical_significance":[],"seq_region_name":"7","id":"rs1795273699"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480909,"feature_type":"variation","strand":1,"end":140480909,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795273741"},{"clinical_significance":[],"id":"rs1020627836","seq_region_name":"7","end":140480911,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140480911,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480912,"source":"dbSNP","strand":1,"feature_type":"variation","end":140480912,"alleles":["T","A"],"id":"rs907087565","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140480913,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140480913,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795273939","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1451512475","clinical_significance":[],"strand":1,"feature_type":"variation","end":140480914,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480914,"source":"dbSNP"},{"alleles":["A","G"],"end":140480915,"strand":1,"feature_type":"variation","start":140480915,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1795274043","clinical_significance":[]},{"seq_region_name":"7","id":"rs1003301691","clinical_significance":[],"end":140480919,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140480919,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480923,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140480923,"id":"rs1795274142","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs956909968","end":140480931,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140480931,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480932,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TT","T"],"end":140480933,"seq_region_name":"7","id":"rs1795274229","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140480934,"alleles":["G","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480934,"clinical_significance":[],"id":"rs1585510290","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480940,"source":"dbSNP","strand":1,"feature_type":"variation","end":140480940,"alleles":["A","C","T"],"seq_region_name":"7","id":"rs1176831406","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795274535","clinical_significance":[],"end":140480945,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140480945,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"alleles":["T","A","G"],"end":140480947,"strand":1,"feature_type":"variation","start":140480947,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs988286548","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1034376827","clinical_significance":[],"end":140480951,"alleles":["C","A","G"],"strand":1,"feature_type":"variation","start":140480951,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"id":"rs1795274958","seq_region_name":"7","source":"dbSNP","start":140480952,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140480952,"alleles":["C","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs10265395","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480955,"feature_type":"variation","strand":1,"end":140480955,"alleles":["G","A","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585510331","source":"dbSNP","start":140480957,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140480957,"alleles":["G","A"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480960,"source":"dbSNP","strand":1,"feature_type":"variation","end":140480960,"alleles":["G","A"],"seq_region_name":"7","id":"rs1795275231","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795275280","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480961,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140480961},{"seq_region_name":"7","id":"rs1795275337","clinical_significance":[],"start":140480962,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140480962,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1265774638","clinical_significance":[],"alleles":["T","C","G"],"end":140480968,"strand":1,"feature_type":"variation","start":140480968,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"id":"rs1795275477","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140480973,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480973,"source":"dbSNP"},{"end":140480974,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140480974,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1795275530","clinical_significance":[]},{"clinical_significance":[],"id":"rs1203947632","seq_region_name":"7","end":140480977,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140480977,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480981,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140480981,"seq_region_name":"7","id":"rs1357499284","clinical_significance":[]},{"seq_region_name":"7","id":"rs1006297456","clinical_significance":[],"strand":1,"feature_type":"variation","end":140480986,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140480986,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1259667790","source":"dbSNP","start":140480990,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140480990,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140480991,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480991,"clinical_significance":[],"id":"rs1016301935","seq_region_name":"7"},{"start":140480992,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","G"],"end":140480992,"strand":1,"feature_type":"variation","id":"rs1795275860","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795275918","seq_region_name":"7","source":"dbSNP","start":140480993,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140480993,"alleles":["A","C"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140480995,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140480995,"clinical_significance":[],"seq_region_name":"7","id":"rs1795275966"},{"start":140480996,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140480996,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs1394330002","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140480997,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140480997,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs2130394161","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795276063","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481000,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140481000},{"seq_region_name":"7","id":"rs764443772","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481007,"source":"dbSNP","strand":1,"feature_type":"variation","end":140481007,"alleles":["T","G"]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481010,"source":"dbSNP","strand":1,"feature_type":"variation","end":140481010,"alleles":["T","C"],"id":"rs1795276170","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1325260782","clinical_significance":[],"alleles":["G","T"],"end":140481011,"strand":1,"feature_type":"variation","start":140481011,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"feature_type":"variation","strand":1,"alleles":["AAAAA","AAAA"],"end":140481032,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481028,"clinical_significance":[],"seq_region_name":"7","id":"rs1795276262"},{"id":"rs1312038888","seq_region_name":"7","clinical_significance":[],"end":140481032,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","start":140481032,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs535877427","clinical_significance":[],"strand":1,"feature_type":"variation","end":140481035,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481035,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1795276500","seq_region_name":"7","source":"dbSNP","start":140481036,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["AA","A"],"end":140481037,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1230187093","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481039,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140481039},{"source":"dbSNP","start":140481039,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["CTCTACTCT","CTCT"],"end":140481047,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs962189862"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481043,"feature_type":"variation","strand":1,"end":140481043,"alleles":["A","C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs76152253"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1303512236","alleles":["C","G"],"end":140481044,"feature_type":"variation","strand":1,"source":"dbSNP","start":140481044,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"start":140481046,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140481046,"strand":1,"feature_type":"variation","id":"rs1585510409","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481048,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140481048,"clinical_significance":[],"id":"rs923532590","seq_region_name":"7"},{"id":"rs1795277020","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481049,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140481049},{"clinical_significance":[],"seq_region_name":"7","id":"rs186303233","feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140481050,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481050},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795277191","feature_type":"variation","strand":1,"end":140481053,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481053},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481057,"feature_type":"variation","strand":1,"end":140481057,"alleles":["T","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs926350175"},{"id":"rs1795277305","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140481059,"strand":1,"feature_type":"variation","start":140481059,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"start":140481060,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140481060,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2082588890","clinical_significance":[]},{"start":140481063,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140481063,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs757815095","clinical_significance":[]},{"id":"rs1211220590","seq_region_name":"7","clinical_significance":[],"start":140481063,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140481075,"alleles":["ATACAATACAATA","ATACAATA"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140481066,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481066,"clinical_significance":[],"seq_region_name":"7","id":"rs1466321753"},{"seq_region_name":"7","id":"rs1482049071","clinical_significance":[],"end":140481067,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140481067,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1281985644","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481067,"source":"dbSNP","strand":1,"feature_type":"variation","end":140481068,"alleles":["AA","AAA"]},{"start":140481068,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140481068,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795277652","clinical_significance":[]},{"start":140481074,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140481079,"alleles":["TATTAT","TAT"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795277703","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795277788","end":140481075,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140481075,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481077,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140481077,"seq_region_name":"7","id":"rs1795277832","clinical_significance":[]},{"seq_region_name":"7","id":"rs1375185849","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481079,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TCTATTAACATTAATCATAGTCTTC","TC"],"end":140481103},{"alleles":["TATTAACATTAATCATA","-"],"end":140481097,"strand":1,"feature_type":"variation","start":140481081,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1180799789","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140481082,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481082,"clinical_significance":[],"seq_region_name":"7","id":"rs1795277966"},{"clinical_significance":[],"seq_region_name":"7","id":"rs941652359","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140481087,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481087},{"id":"rs1261747062","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140481088,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481088,"source":"dbSNP"},{"alleles":["T","C"],"end":140481090,"feature_type":"variation","strand":1,"source":"dbSNP","start":140481090,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1430245243"},{"end":140481093,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140481093,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1795278133","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481095,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140481095,"seq_region_name":"7","id":"rs1186594197","clinical_significance":[]},{"end":140481098,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140481098,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130394380"},{"seq_region_name":"7","id":"rs1389385218","clinical_significance":[],"end":140481104,"alleles":["TCTTCC","-"],"strand":1,"feature_type":"variation","start":140481099,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs750010226","source":"dbSNP","start":140481100,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140481100,"feature_type":"variation","strand":1},{"end":140481103,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140481103,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs973184649","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130394419","feature_type":"variation","strand":1,"end":140481104,"alleles":["CC","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481103},{"clinical_significance":[],"seq_region_name":"7","id":"rs566316006","source":"dbSNP","start":140481104,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140481104,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140481105,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140481105,"alleles":["G","A","C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs191215744","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481107,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140481107,"id":"rs1202683076","seq_region_name":"7","clinical_significance":[]},{"id":"rs1051568875","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481108,"source":"dbSNP","strand":1,"feature_type":"variation","end":140481108,"alleles":["G","A","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795278643","alleles":["C","T"],"end":140481111,"feature_type":"variation","strand":1,"source":"dbSNP","start":140481111,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs890272927","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481112,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140481112},{"seq_region_name":"7","id":"rs1795278760","clinical_significance":[],"start":140481114,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140481113,"alleles":["-","CG"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs943321766","seq_region_name":"7","source":"dbSNP","start":140481114,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140481114,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795278854","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140481118,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481118,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1464689119","alleles":["A","G"],"end":140481124,"feature_type":"variation","strand":1,"source":"dbSNP","start":140481124,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1302349847","clinical_significance":[],"start":140481125,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","G"],"end":140481125,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1454496916","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140481126,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481126},{"alleles":["T","C"],"end":140481129,"feature_type":"variation","strand":1,"source":"dbSNP","start":140481129,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795279063"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140481131,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481131,"source":"dbSNP","seq_region_name":"7","id":"rs1795279108","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481133,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140481133,"clinical_significance":[],"seq_region_name":"7","id":"rs1795279148"},{"strand":1,"feature_type":"variation","end":140481136,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481136,"source":"dbSNP","seq_region_name":"7","id":"rs1795279192","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795279241","seq_region_name":"7","feature_type":"variation","strand":1,"end":140481139,"alleles":["A","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481139},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795279279","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481147,"feature_type":"variation","strand":1,"alleles":["-","A"],"end":140481146},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481148,"feature_type":"variation","strand":1,"end":140481148,"alleles":["G","A"],"clinical_significance":[],"id":"rs1795279313","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795279357","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481149,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140481149},{"seq_region_name":"7","id":"rs2130394555","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140481150,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481150,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140481151,"alleles":["G","A","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481151,"clinical_significance":[],"seq_region_name":"7","id":"rs1380734398"},{"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140481155,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481155,"source":"dbSNP","seq_region_name":"7","id":"rs1385672356","clinical_significance":[]},{"start":140481156,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140481156,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","id":"rs1466367528","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1166535581","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481159,"source":"dbSNP","strand":1,"feature_type":"variation","end":140481159,"alleles":["C","G","T"]},{"feature_type":"variation","strand":1,"end":140481160,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481160,"clinical_significance":[],"seq_region_name":"7","id":"rs1795279606"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1039358806","source":"dbSNP","start":140481161,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140481161,"alleles":["G","A","T"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140481162,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140481162,"alleles":["A","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs899831556"},{"alleles":["A","T"],"end":140481165,"feature_type":"variation","strand":1,"source":"dbSNP","start":140481165,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1461740779"},{"id":"rs2130394608","seq_region_name":"7","clinical_significance":[],"end":140481167,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140481167,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"source":"dbSNP","start":140481171,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140481171,"alleles":["T","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs923472209","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1001238477","clinical_significance":[],"alleles":["C","T"],"end":140481189,"strand":1,"feature_type":"variation","start":140481189,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481190,"source":"dbSNP","strand":1,"feature_type":"variation","end":140481190,"alleles":["C","T"],"seq_region_name":"7","id":"rs544936460","clinical_significance":[]},{"alleles":["A","C","G"],"end":140481192,"strand":1,"feature_type":"variation","start":140481192,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs892580071","clinical_significance":[]},{"id":"rs1235518568","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140481193,"alleles":["G","C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481193,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795280107","feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140481200,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481200},{"seq_region_name":"7","id":"rs1009643557","clinical_significance":[],"end":140481201,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140481201,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"start":140481202,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140481202,"strand":1,"feature_type":"variation","id":"rs1585510606","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795280262","feature_type":"variation","strand":1,"end":140481203,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481203},{"seq_region_name":"7","id":"rs1252143082","clinical_significance":[],"start":140481208,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","C","T"],"end":140481208,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795280361","end":140481211,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140481211,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs2130394687","clinical_significance":[],"end":140481212,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140481212,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs942340373","clinical_significance":[],"alleles":["C","G","T"],"end":140481214,"strand":1,"feature_type":"variation","start":140481214,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140481217,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481217,"source":"dbSNP","seq_region_name":"7","id":"rs1795280436","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481219,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140481219,"clinical_significance":[],"id":"rs1795280469","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140481221,"alleles":["C","-"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481221,"source":"dbSNP","seq_region_name":"7","id":"rs1338567201","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795280540","source":"dbSNP","start":140481221,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140481223,"alleles":["CAA","-"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs371114658","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481222,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140481222},{"feature_type":"variation","strand":1,"end":140481226,"alleles":["A","C","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481226,"clinical_significance":[],"seq_region_name":"7","id":"rs73480279"},{"seq_region_name":"7","id":"rs1795280714","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481227,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140481227},{"seq_region_name":"7","id":"rs1248137249","clinical_significance":[],"strand":1,"feature_type":"variation","end":140481229,"alleles":["A","AA"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481229,"source":"dbSNP"},{"alleles":["A","G"],"end":140481229,"feature_type":"variation","strand":1,"source":"dbSNP","start":140481229,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795280762"},{"seq_region_name":"7","id":"rs778631876","clinical_significance":[],"end":140481236,"alleles":["AAAAAA","AAAA","AAAAAAA"],"strand":1,"feature_type":"variation","start":140481231,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"strand":1,"feature_type":"variation","end":140481235,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481235,"source":"dbSNP","seq_region_name":"7","id":"rs1795280938","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795280984","alleles":["A","G"],"end":140481236,"feature_type":"variation","strand":1,"source":"dbSNP","start":140481236,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"start":140481239,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","C","G"],"end":140481239,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs576729608","clinical_significance":[]},{"end":140481240,"alleles":["AG","GC"],"strand":1,"feature_type":"variation","start":140481239,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs386718467","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140481240,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481240,"clinical_significance":[],"seq_region_name":"7","id":"rs115197246"},{"seq_region_name":"7","id":"rs1795281137","clinical_significance":[],"strand":1,"feature_type":"variation","end":140481245,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481245,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs556326467","source":"dbSNP","start":140481246,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140481246,"alleles":["C","T"],"feature_type":"variation","strand":1},{"end":140481247,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140481247,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1391028063","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795281254","clinical_significance":[],"start":140481252,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140481253,"alleles":["GG","G"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140481258,"alleles":["T","C","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481258,"source":"dbSNP","seq_region_name":"7","id":"rs1585510661","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130394825","clinical_significance":[],"start":140481259,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140481259,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481260,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140481260,"id":"rs1247305179","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1391967560","clinical_significance":[],"start":140481262,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140481262,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481265,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140481265,"seq_region_name":"7","id":"rs1305296639","clinical_significance":[]},{"start":140481271,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140481271,"alleles":["A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585510673","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1423316423","feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140481279,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481279},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481281,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140481281,"id":"rs1162381951","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140481287,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481287,"clinical_significance":[],"seq_region_name":"7","id":"rs963089921"},{"start":140481290,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["GCAGGAGAATGGCGTGAACCCGGCAGGTG","GCAGGAGAATGGCGTGAACCCGGCAGGTGCAGGAGAATGGCGTGAACCCGGCAGGTG"],"end":140481318,"strand":1,"feature_type":"variation","id":"rs1195286921","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795281741","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481292,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140481292},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585510687","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481295,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140481295},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795281818","feature_type":"variation","strand":1,"end":140481300,"alleles":["G","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481300},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795281849","source":"dbSNP","start":140481301,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140481301,"alleles":["G","A"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481302,"source":"dbSNP","strand":1,"feature_type":"variation","end":140481302,"alleles":["C","T"],"seq_region_name":"7","id":"rs563032466","clinical_significance":[]},{"clinical_significance":[],"id":"rs374523153","seq_region_name":"7","source":"dbSNP","start":140481303,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140481303,"alleles":["G","A","T"],"feature_type":"variation","strand":1},{"start":140481305,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140481305,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs1179279245","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795282044","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481306,"feature_type":"variation","strand":1,"end":140481306,"alleles":["A","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795282084","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481308,"feature_type":"variation","strand":1,"alleles":["CCCGGCAGGTGAGGCTTGCAGTGAGCTGAGATC","C"],"end":140481340},{"strand":1,"feature_type":"variation","end":140481309,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481309,"source":"dbSNP","seq_region_name":"7","id":"rs1055629011","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs894521377","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481310,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140481310},{"id":"rs749979351","seq_region_name":"7","clinical_significance":[],"start":140481311,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140481311,"alleles":["G","A","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1006139004","seq_region_name":"7","alleles":["G","T"],"end":140481312,"feature_type":"variation","strand":1,"source":"dbSNP","start":140481312,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140481315,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140481315,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1175620490"},{"clinical_significance":[],"seq_region_name":"7","id":"rs929085711","source":"dbSNP","start":140481316,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140481316,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1585510714","clinical_significance":[],"start":140481317,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C","G"],"end":140481317,"strand":1,"feature_type":"variation"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481318,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140481318,"clinical_significance":[],"seq_region_name":"7","id":"rs1290868033"},{"id":"rs1795282473","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481318,"source":"dbSNP","strand":1,"feature_type":"variation","end":140481318,"alleles":["G","GG"]},{"start":140481319,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140481319,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130394982","clinical_significance":[]},{"source":"dbSNP","start":140481320,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140481320,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130394987"},{"id":"rs530538481","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140481325,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481325,"source":"dbSNP"},{"alleles":["T","C"],"end":140481329,"strand":1,"feature_type":"variation","start":140481329,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1585510739","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481330,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140481330,"seq_region_name":"7","id":"rs1353008083","clinical_significance":[]},{"end":140481333,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140481333,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795282672"},{"seq_region_name":"7","id":"rs1277833110","clinical_significance":[],"start":140481334,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140481334,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1795282761","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481336,"feature_type":"variation","strand":1,"end":140481336,"alleles":["A","C","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795282801","source":"dbSNP","start":140481337,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140481337,"feature_type":"variation","strand":1},{"end":140481342,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140481342,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1238655624","seq_region_name":"7"},{"alleles":["A","C"],"end":140481346,"strand":1,"feature_type":"variation","start":140481346,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1585510758","clinical_significance":[]},{"start":140481351,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140481351,"alleles":["C","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795282930","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130395046","end":140481353,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140481353,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1741785135","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481357,"source":"dbSNP","strand":1,"feature_type":"variation","end":140481357,"alleles":["G","A"]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481359,"feature_type":"variation","strand":1,"end":140481359,"alleles":["C","G"],"clinical_significance":[],"id":"rs1795282970","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140481363,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481363,"source":"dbSNP","seq_region_name":"7","id":"rs1563102023","clinical_significance":[]},{"seq_region_name":"7","id":"rs1331847798","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140481364,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481364,"source":"dbSNP"},{"end":140481370,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140481370,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1795283110","seq_region_name":"7","clinical_significance":[]},{"start":140481371,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A","T"],"end":140481371,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1455384661","clinical_significance":[]},{"source":"dbSNP","start":140481373,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140481373,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795283210"},{"alleles":["G","A"],"end":140481375,"feature_type":"variation","strand":1,"source":"dbSNP","start":140481375,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs541859577"},{"start":140481376,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140481376,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795283271","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795283293","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481377,"feature_type":"variation","strand":1,"end":140481377,"alleles":["C","T"]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481378,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140481378,"clinical_significance":[],"seq_region_name":"7","id":"rs962076053"},{"id":"rs1299400066","seq_region_name":"7","clinical_significance":[],"start":140481379,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140481379,"alleles":["G","A","C"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140481382,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","A","C"],"end":140481382,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1318578861"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795283488","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481383,"feature_type":"variation","strand":1,"end":140481382,"alleles":["-","A","AA"]},{"alleles":["C","A"],"end":140481383,"strand":1,"feature_type":"variation","start":140481383,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1386545533","seq_region_name":"7","clinical_significance":[]},{"alleles":["AAAAAAAAAAAAAAA","AAAAAAAAAAAAA","AAAAAAAAAAAAAA","AAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAA"],"end":140481398,"feature_type":"variation","strand":1,"source":"dbSNP","start":140481384,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs11398120"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481385,"feature_type":"variation","strand":1,"end":140481385,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1388577072"},{"start":140481387,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140481387,"alleles":["A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795283817","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795283863","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481388,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140481388},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140481390,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481390,"source":"dbSNP","seq_region_name":"7","id":"rs1479372589","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1442211654","end":140481393,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140481393,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140481397,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140481397,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795284083"},{"seq_region_name":"7","id":"rs1795284124","clinical_significance":[],"end":140481402,"alleles":["ATCAT","AT"],"strand":1,"feature_type":"variation","start":140481398,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs994093256","end":140481399,"alleles":["T","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140481399,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795284222","clinical_significance":[],"end":140481400,"alleles":["TC","-"],"strand":1,"feature_type":"variation","start":140481399,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"id":"rs1216473337","seq_region_name":"7","clinical_significance":[],"start":140481400,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140481400,"alleles":["C","A","T"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140481401,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481401,"source":"dbSNP","seq_region_name":"7","id":"rs1795284297","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140481402,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481402,"source":"dbSNP","seq_region_name":"7","id":"rs911763411","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795284366","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481403,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140481403},{"end":140481406,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140481406,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs943166182","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140481410,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481410,"source":"dbSNP","seq_region_name":"7","id":"rs1795284448","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795284476","feature_type":"variation","strand":1,"end":140481412,"alleles":["G","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481412},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481413,"feature_type":"variation","strand":1,"end":140481413,"alleles":["T","G"],"clinical_significance":[],"id":"rs1585510827","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1030524965","clinical_significance":[],"start":140481415,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140481415,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1204570986","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140481416,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481416,"source":"dbSNP"},{"id":"rs955032815","seq_region_name":"7","clinical_significance":[],"start":140481419,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140481419,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"start":140481420,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140481420,"alleles":["T","G"],"strand":1,"feature_type":"variation","id":"rs1365927618","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1218341504","source":"dbSNP","start":140481425,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140481425,"feature_type":"variation","strand":1},{"end":140481432,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140481432,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795284757"},{"clinical_significance":[],"seq_region_name":"7","id":"rs986436969","source":"dbSNP","start":140481433,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140481433,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795284846","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481434,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140481434},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481435,"source":"dbSNP","strand":1,"feature_type":"variation","end":140481435,"alleles":["T","C"],"seq_region_name":"7","id":"rs1795284877","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795284905","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481439,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140481439},{"strand":1,"feature_type":"variation","end":140481442,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481442,"source":"dbSNP","seq_region_name":"7","id":"rs182260599","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481444,"feature_type":"variation","strand":1,"end":140481444,"alleles":["T","G"],"clinical_significance":[],"id":"rs1795284938","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481449,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140481449,"seq_region_name":"7","id":"rs1795284972","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795285002","feature_type":"variation","strand":1,"end":140481454,"alleles":["C","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481454},{"strand":1,"feature_type":"variation","end":140481456,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481456,"source":"dbSNP","seq_region_name":"7","id":"rs963713218","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140481465,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481465,"source":"dbSNP","seq_region_name":"7","id":"rs1563102059","clinical_significance":[]},{"clinical_significance":[],"id":"rs186086151","seq_region_name":"7","source":"dbSNP","start":140481466,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140481466,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795285142","clinical_significance":[],"start":140481471,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140481471,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795285174","end":140481473,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140481473,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140481476,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140481476,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs904416625"},{"start":140481477,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140481477,"alleles":["T","-"],"strand":1,"feature_type":"variation","id":"rs1795285235","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","A"],"end":140481478,"strand":1,"feature_type":"variation","start":140481478,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs989784074","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481480,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140481480,"clinical_significance":[],"seq_region_name":"7","id":"rs914343501"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795285305","alleles":["C","T"],"end":140481481,"feature_type":"variation","strand":1,"source":"dbSNP","start":140481481,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"end":140481482,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140481482,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1406173360","clinical_significance":[]},{"seq_region_name":"7","id":"rs945839569","clinical_significance":[],"alleles":["C","T"],"end":140481483,"strand":1,"feature_type":"variation","start":140481483,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"strand":1,"feature_type":"variation","alleles":["CCCC","CCCCC"],"end":140481490,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481487,"source":"dbSNP","seq_region_name":"7","id":"rs1467883792","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140481491,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481491,"clinical_significance":[],"seq_region_name":"7","id":"rs1795285927"},{"clinical_significance":[],"id":"rs368181433","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140481496,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481496},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481497,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140481497,"seq_region_name":"7","id":"rs1041844843","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795286084","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481499,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140481499},{"id":"rs1795286127","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["CCTGG","-"],"end":140481503,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481499,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795286156","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140481504,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481504,"source":"dbSNP"},{"id":"rs1795286189","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481509,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140481509},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795286226","feature_type":"variation","strand":1,"end":140481513,"alleles":["G","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481513},{"start":140481514,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140481514,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1476358327","clinical_significance":[]},{"id":"rs1795286289","seq_region_name":"7","clinical_significance":[],"end":140481516,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140481516,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"source":"dbSNP","start":140481516,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["CTACTCTGTTGCTATGTATTCAACTTTTTCACATCTTCAC","CTACTCTGTTGCTATGTATTCAACTTTTTCACATCTTCACTACTCTGTTGCTATGTATTCAACTTTTTCACATCTTCAC"],"end":140481555,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130395535"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795286316","source":"dbSNP","start":140481518,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140481518,"alleles":["A","G"],"feature_type":"variation","strand":1},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481519,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140481519,"clinical_significance":[],"seq_region_name":"7","id":"rs1563102074"},{"start":140481520,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","A"],"end":140481520,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795286378","clinical_significance":[]},{"start":140481521,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140481521,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1468869672","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1192378240","alleles":["T","G"],"end":140481524,"feature_type":"variation","strand":1,"source":"dbSNP","start":140481524,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs2130395579","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481525,"source":"dbSNP","strand":1,"feature_type":"variation","end":140481525,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130395588","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140481526,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481526},{"alleles":["C","G"],"end":140481536,"feature_type":"variation","strand":1,"source":"dbSNP","start":140481536,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs754558111"},{"seq_region_name":"7","id":"rs1795286530","clinical_significance":[],"strand":1,"feature_type":"variation","end":140481538,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481538,"source":"dbSNP"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481545,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140481545,"clinical_significance":[],"seq_region_name":"7","id":"rs1461875290"},{"id":"rs935917347","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140481550,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481550,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140481554,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481554,"clinical_significance":[],"seq_region_name":"7","id":"rs928520689"},{"clinical_significance":[],"id":"rs6967008","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140481555,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481555},{"seq_region_name":"7","id":"rs1055642410","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481556,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140481556},{"seq_region_name":"7","id":"rs1216636749","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481556,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","-"],"end":140481556},{"clinical_significance":[],"id":"rs1270200882","seq_region_name":"7","feature_type":"variation","strand":1,"end":140481560,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481560},{"start":140481561,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140481561,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1449381570","clinical_significance":[]},{"seq_region_name":"7","id":"rs144203966","clinical_significance":[],"strand":1,"feature_type":"variation","end":140481562,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481562,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140481576,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481576,"source":"dbSNP","id":"rs1009695446","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140481577,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481577,"clinical_significance":[],"seq_region_name":"7","id":"rs531430897"},{"source":"dbSNP","start":140481580,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140481580,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1585510970","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140481591,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481591,"clinical_significance":[],"id":"rs1795287116","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1795287137","seq_region_name":"7","alleles":["G","T"],"end":140481593,"feature_type":"variation","strand":1,"source":"dbSNP","start":140481593,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs148727267","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481594,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140481594},{"source":"dbSNP","start":140481595,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140481595,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1037644942","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481602,"source":"dbSNP","strand":1,"feature_type":"variation","end":140481602,"alleles":["C","G"],"seq_region_name":"7","id":"rs1795287202","clinical_significance":[]},{"id":"rs142338845","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140481609,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481609,"source":"dbSNP"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481610,"feature_type":"variation","strand":1,"end":140481610,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130395714"},{"clinical_significance":[],"id":"rs1473667329","seq_region_name":"7","source":"dbSNP","start":140481613,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140481613,"alleles":["A","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795287284","clinical_significance":[],"end":140481614,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140481614,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1795287300","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481615,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140481615},{"clinical_significance":[],"seq_region_name":"7","id":"rs1002755544","source":"dbSNP","start":140481616,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140481616,"alleles":["T","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1033953680","end":140481619,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140481619,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140481620,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481620,"clinical_significance":[],"seq_region_name":"7","id":"rs1795287352"},{"seq_region_name":"7","id":"rs1030825612","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481621,"source":"dbSNP","strand":1,"feature_type":"variation","end":140481621,"alleles":["C","A","T"]},{"alleles":["G","T"],"end":140481623,"strand":1,"feature_type":"variation","start":140481623,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1795287367","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795287388","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140481624,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481624},{"source":"dbSNP","start":140481629,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140481629,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795287410"},{"clinical_significance":[],"seq_region_name":"7","id":"rs529371467","feature_type":"variation","strand":1,"end":140481630,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481630},{"id":"rs973666040","seq_region_name":"7","clinical_significance":[],"start":140481632,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140481632,"alleles":["A","C","G"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481634,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140481634,"seq_region_name":"7","id":"rs2130395752","clinical_significance":[]},{"source":"dbSNP","start":140481636,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140481636,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795287499"},{"strand":1,"feature_type":"variation","end":140481640,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481640,"source":"dbSNP","id":"rs1795287522","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","T"],"end":140481641,"feature_type":"variation","strand":1,"source":"dbSNP","start":140481641,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795287769","seq_region_name":"7"},{"end":140481651,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140481651,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1795287782","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795287827","source":"dbSNP","start":140481655,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140481655,"feature_type":"variation","strand":1},{"id":"rs1585510992","seq_region_name":"7","clinical_significance":[],"alleles":["A","G"],"end":140481656,"strand":1,"feature_type":"variation","start":140481656,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1167514237","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481660,"source":"dbSNP","strand":1,"feature_type":"variation","end":140481660,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs2130395782","clinical_significance":[],"start":140481660,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["AGGTAGTAACCTTTAGAGACACAATAGGT","AGGT"],"end":140481688,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1461050453","end":140481661,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140481661,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481672,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140481672,"seq_region_name":"7","id":"rs1348555961","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1206889184","feature_type":"variation","strand":1,"end":140481676,"alleles":["A","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481676},{"strand":1,"feature_type":"variation","alleles":["C","CC"],"end":140481679,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481679,"source":"dbSNP","seq_region_name":"7","id":"rs2130395799","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481680,"source":"dbSNP","strand":1,"feature_type":"variation","end":140481680,"alleles":["A","G"],"seq_region_name":"7","id":"rs1306184650","clinical_significance":[]},{"seq_region_name":"7","id":"rs1025969905","clinical_significance":[],"strand":1,"feature_type":"variation","end":140481684,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481684,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585511003","feature_type":"variation","strand":1,"alleles":["GG","-"],"end":140481687,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481686},{"clinical_significance":[],"seq_region_name":"7","id":"rs950383167","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481687,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140481687},{"end":140481690,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140481690,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs987182622","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140481693,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481693,"source":"dbSNP","seq_region_name":"7","id":"rs1795288041","clinical_significance":[]},{"id":"rs1585511010","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140481694,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481694,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs911606073","end":140481696,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140481696,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"alleles":["T","G"],"end":140481709,"strand":1,"feature_type":"variation","start":140481709,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs964585813","clinical_significance":[]},{"start":140481714,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140481714,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1377801445","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130395842","source":"dbSNP","start":140481715,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140481715,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140481716,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481716,"clinical_significance":[],"seq_region_name":"7","id":"rs1298448461"},{"start":140481720,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140481727,"alleles":["TCAGACTC","TC"],"strand":1,"feature_type":"variation","id":"rs1795288174","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1443896679","clinical_significance":[],"end":140481723,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140481723,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140481724,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481724,"clinical_significance":[],"seq_region_name":"7","id":"rs1352581477"},{"seq_region_name":"7","id":"rs1287163175","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481726,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140481726},{"end":140481727,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140481727,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1327890604","clinical_significance":[]},{"seq_region_name":"7","id":"rs1425244760","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481728,"source":"dbSNP","strand":1,"feature_type":"variation","end":140481728,"alleles":["T","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs547728460","feature_type":"variation","strand":1,"end":140481729,"alleles":["C","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481729},{"start":140481730,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","T"],"end":140481730,"strand":1,"feature_type":"variation","id":"rs1386951082","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481731,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140481731,"seq_region_name":"7","id":"rs1334914156","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs975007689","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481741,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140481741},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481746,"source":"dbSNP","strand":1,"feature_type":"variation","end":140481746,"alleles":["G","A"],"seq_region_name":"7","id":"rs2130395885","clinical_significance":[]},{"seq_region_name":"7","id":"rs967440263","clinical_significance":[],"strand":1,"feature_type":"variation","end":140481748,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481748,"source":"dbSNP"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481749,"feature_type":"variation","strand":1,"end":140481749,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs925798227"},{"clinical_significance":[],"seq_region_name":"7","id":"rs928335540","source":"dbSNP","start":140481751,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140481751,"alleles":["G","A"],"feature_type":"variation","strand":1},{"start":140481752,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","T"],"end":140481752,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130395902","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795288565","clinical_significance":[],"alleles":["G","A"],"end":140481757,"strand":1,"feature_type":"variation","start":140481757,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"alleles":["G","T"],"end":140481758,"strand":1,"feature_type":"variation","start":140481758,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs938537881","seq_region_name":"7","clinical_significance":[]},{"end":140481762,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140481762,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs991253825","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140481763,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481763,"clinical_significance":[],"seq_region_name":"7","id":"rs1585511059"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481764,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140481764,"seq_region_name":"7","id":"rs1795288724","clinical_significance":[]},{"clinical_significance":[],"id":"rs1490984449","seq_region_name":"7","end":140481765,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140481765,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140481766,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140481766,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs565954459"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481767,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140481767,"clinical_significance":[],"seq_region_name":"7","id":"rs532806672"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481770,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140481770,"seq_region_name":"7","id":"rs1795288817","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795288861","clinical_significance":[],"strand":1,"feature_type":"variation","end":140481773,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481773,"source":"dbSNP"},{"seq_region_name":"7","id":"rs913907732","clinical_significance":[],"end":140481774,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140481774,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"alleles":["T","C"],"end":140481776,"feature_type":"variation","strand":1,"source":"dbSNP","start":140481776,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795288900","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795288924","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140481777,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481777},{"id":"rs1795288944","seq_region_name":"7","clinical_significance":[],"start":140481778,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140481778,"strand":1,"feature_type":"variation"},{"start":140481779,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140481779,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1225146909","clinical_significance":[]},{"source":"dbSNP","start":140481780,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140481780,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795288990","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1370662357","source":"dbSNP","start":140481784,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140481784,"alleles":["A","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795289017","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481785,"source":"dbSNP","strand":1,"feature_type":"variation","end":140481785,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs945326629","clinical_significance":[],"end":140481787,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140481787,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"source":"dbSNP","start":140481788,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140481788,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1405261692"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481789,"source":"dbSNP","strand":1,"feature_type":"variation","end":140481789,"alleles":["G","A"],"seq_region_name":"7","id":"rs528140877","clinical_significance":[]},{"alleles":["C","T"],"end":140481791,"feature_type":"variation","strand":1,"source":"dbSNP","start":140481791,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1585511080","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140481795,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481795,"clinical_significance":[],"seq_region_name":"7","id":"rs1037571194"},{"start":140481798,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140481798,"alleles":["T","G"],"strand":1,"feature_type":"variation","id":"rs1180288832","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140481801,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481801,"clinical_significance":[],"seq_region_name":"7","id":"rs1795289150"},{"start":140481802,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140481802,"strand":1,"feature_type":"variation","id":"rs1301281362","seq_region_name":"7","clinical_significance":[]},{"id":"rs1795289193","seq_region_name":"7","clinical_significance":[],"start":140481814,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["AAG","AAGAAG"],"end":140481816,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481817,"source":"dbSNP","strand":1,"feature_type":"variation","end":140481817,"alleles":["G","A","C"],"seq_region_name":"7","id":"rs1457324685","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795289239","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481819,"feature_type":"variation","strand":1,"end":140481819,"alleles":["A","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1345907522","feature_type":"variation","strand":1,"end":140481821,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481821},{"feature_type":"variation","strand":1,"end":140481823,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481823,"clinical_significance":[],"seq_region_name":"7","id":"rs191330556"},{"end":140481832,"alleles":["CTAGCTTCT","CTAGCTTCTAGCTTCT"],"strand":1,"feature_type":"variation","start":140481824,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1795289560","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140481825,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140481825,"alleles":["T","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1417583832"},{"end":140481826,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140481826,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795289609","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1475565121","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481827,"feature_type":"variation","strand":1,"end":140481827,"alleles":["G","C"]},{"id":"rs929258492","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481828,"source":"dbSNP","strand":1,"feature_type":"variation","end":140481828,"alleles":["C","T"]},{"end":140481834,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140481834,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1795289699","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140481836,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481836,"clinical_significance":[],"seq_region_name":"7","id":"rs906593331"},{"strand":1,"feature_type":"variation","alleles":["A","C","T"],"end":140481840,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481840,"source":"dbSNP","seq_region_name":"7","id":"rs986792188","clinical_significance":[]},{"alleles":["CTT","-"],"end":140481843,"feature_type":"variation","strand":1,"source":"dbSNP","start":140481841,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1481655245"},{"end":140481841,"alleles":["-","A"],"strand":1,"feature_type":"variation","start":140481842,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1795289770","clinical_significance":[]},{"seq_region_name":"7","id":"rs1217235416","clinical_significance":[],"alleles":["T","C"],"end":140481842,"strand":1,"feature_type":"variation","start":140481842,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481842,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TTTTTTTTTTTTTTTT","TTTTTTTTTTTT","TTTTTTTTTTTTT","TTTTTTTTTTTTTT","TTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTT"],"end":140481857,"seq_region_name":"7","id":"rs201790890","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140481845,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481845,"clinical_significance":[],"seq_region_name":"7","id":"rs1314767355"},{"end":140481846,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140481846,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795289817","seq_region_name":"7"},{"end":140481847,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140481847,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1184149101","clinical_significance":[]},{"id":"rs1795289849","seq_region_name":"7","clinical_significance":[],"start":140481850,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","G"],"end":140481850,"strand":1,"feature_type":"variation"},{"alleles":["T","C"],"end":140481851,"feature_type":"variation","strand":1,"source":"dbSNP","start":140481851,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1412299927","seq_region_name":"7"},{"source":"dbSNP","start":140481858,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140481858,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1171573733"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795289909","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481858,"feature_type":"variation","strand":1,"alleles":["G","-"],"end":140481858},{"clinical_significance":[],"seq_region_name":"7","id":"rs1281112115","source":"dbSNP","start":140481860,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140481860,"alleles":["G","T"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140481862,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140481862,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1386174199"},{"seq_region_name":"7","id":"rs1427497494","clinical_significance":[],"strand":1,"feature_type":"variation","end":140481862,"alleles":["-","GG"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481863,"source":"dbSNP"},{"seq_region_name":"7","id":"rs561571561","clinical_significance":[],"end":140481863,"alleles":["C","A","G","T"],"strand":1,"feature_type":"variation","start":140481863,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"source":"dbSNP","start":140481864,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140481864,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1355595141"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140481865,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481865,"source":"dbSNP","seq_region_name":"7","id":"rs1449626032","clinical_significance":[]},{"id":"rs1051863008","seq_region_name":"7","clinical_significance":[],"alleles":["C","G","T"],"end":140481866,"strand":1,"feature_type":"variation","start":140481866,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"feature_type":"variation","strand":1,"end":140481867,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481867,"clinical_significance":[],"seq_region_name":"7","id":"rs1378366895"},{"source":"dbSNP","start":140481868,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140481868,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1215021190"},{"source":"dbSNP","start":140481869,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140481869,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1177479692"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481872,"source":"dbSNP","strand":1,"feature_type":"variation","end":140481872,"alleles":["C","T"],"seq_region_name":"7","id":"rs1471058550","clinical_significance":[]},{"id":"rs1795290190","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140481874,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481874,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140481876,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481876,"source":"dbSNP","seq_region_name":"7","id":"rs1427677983","clinical_significance":[]},{"source":"dbSNP","start":140481877,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140481876,"alleles":["-","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1274940449"},{"seq_region_name":"7","id":"rs1339795431","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140481877,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481877,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs570245197","alleles":["C","G","T"],"end":140481878,"feature_type":"variation","strand":1,"source":"dbSNP","start":140481878,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1274156729","alleles":["G","A"],"end":140481882,"feature_type":"variation","strand":1,"source":"dbSNP","start":140481882,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1645367040","feature_type":"variation","strand":1,"end":140481885,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481885},{"seq_region_name":"7","id":"rs1486096913","clinical_significance":[],"start":140481886,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A","T"],"end":140481886,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585511142","source":"dbSNP","start":140481887,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140481887,"feature_type":"variation","strand":1},{"id":"rs1585511145","seq_region_name":"7","clinical_significance":[],"end":140481889,"alleles":["T","A","G"],"strand":1,"feature_type":"variation","start":140481889,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"source":"dbSNP","start":140481890,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140481890,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795290369"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1055730412","feature_type":"variation","strand":1,"end":140481891,"alleles":["C","G","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481891},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140481893,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481893,"source":"dbSNP","seq_region_name":"7","id":"rs1795290416","clinical_significance":[]},{"source":"dbSNP","start":140481895,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140481895,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795290436"},{"seq_region_name":"7","id":"rs537680135","clinical_significance":[],"start":140481897,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140481897,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140481898,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481898,"source":"dbSNP","seq_region_name":"7","id":"rs1472758363","clinical_significance":[]},{"source":"dbSNP","start":140481898,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140481908,"alleles":["GCGATCTCGGC","GC"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130396134"},{"clinical_significance":[],"id":"rs1187608398","seq_region_name":"7","feature_type":"variation","strand":1,"end":140481899,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481899},{"source":"dbSNP","start":140481900,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140481900,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs541737712","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1325201534","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140481902,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481902},{"seq_region_name":"7","id":"rs1026483652","clinical_significance":[],"strand":1,"feature_type":"variation","end":140481905,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481905,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795290675","source":"dbSNP","start":140481906,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140481906,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1448020618","clinical_significance":[],"start":140481906,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140481914,"alleles":["GGCTCACTG","GGCTCACTGGCTCACTG"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140481913,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140481913,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1167617060","seq_region_name":"7"},{"source":"dbSNP","start":140481917,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140481917,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585511162"},{"source":"dbSNP","start":140481922,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140481922,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1017809380"},{"id":"rs1415763704","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140481925,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481925,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1297705925","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481926,"source":"dbSNP","strand":1,"feature_type":"variation","end":140481926,"alleles":["T","G"]},{"alleles":["C","A"],"end":140481927,"feature_type":"variation","strand":1,"source":"dbSNP","start":140481927,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795290867"},{"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140481928,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481928,"source":"dbSNP","seq_region_name":"7","id":"rs1380432695","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481929,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140481929,"id":"rs71552618","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs182847920","clinical_significance":[],"strand":1,"feature_type":"variation","end":140481930,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481930,"source":"dbSNP"},{"start":140481931,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140481931,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795291002","clinical_significance":[]},{"start":140481932,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140481932,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs370315151","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481935,"source":"dbSNP","strand":1,"feature_type":"variation","end":140481935,"alleles":["T","A","C"],"seq_region_name":"7","id":"rs202049304","clinical_significance":[]},{"seq_region_name":"7","id":"rs1299711211","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481939,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140481939},{"alleles":["A","C","G"],"end":140481940,"feature_type":"variation","strand":1,"source":"dbSNP","start":140481940,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs200340951","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481944,"source":"dbSNP","strand":1,"feature_type":"variation","end":140481944,"alleles":["C","T"],"id":"rs1375129416","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","C"],"end":140481945,"strand":1,"feature_type":"variation","start":140481945,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs974511788","clinical_significance":[]},{"alleles":["C","A"],"end":140481947,"strand":1,"feature_type":"variation","start":140481947,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1795291606","clinical_significance":[]},{"clinical_significance":[],"id":"rs1169017339","seq_region_name":"7","end":140481951,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140481951,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140481959,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481959,"clinical_significance":[],"seq_region_name":"7","id":"rs1795291682"},{"end":140481960,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140481960,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1011195799"},{"start":140481961,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","A","T"],"end":140481961,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1227429184","clinical_significance":[]},{"id":"rs1303806031","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140481962,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481962,"source":"dbSNP"},{"source":"dbSNP","start":140481964,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140481964,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795291785","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1021621447","alleles":["C","G"],"end":140481968,"feature_type":"variation","strand":1,"source":"dbSNP","start":140481968,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481974,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140481974,"id":"rs1348883423","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1202323356","clinical_significance":[],"start":140481977,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140481977,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140481980,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140481980,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1276670544","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130396238","alleles":["AC","-"],"end":140481981,"feature_type":"variation","strand":1,"source":"dbSNP","start":140481980,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140481981,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481981,"source":"dbSNP","id":"rs1795291922","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs571969133","seq_region_name":"7","feature_type":"variation","strand":1,"end":140481982,"alleles":["G","A","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481982},{"clinical_significance":[],"seq_region_name":"7","id":"rs1480862492","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481983,"feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140481983},{"start":140481985,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140481985,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs1252817209","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs550891112","source":"dbSNP","start":140481986,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140481986,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1341310173","seq_region_name":"7","alleles":["C","T"],"end":140481987,"feature_type":"variation","strand":1,"source":"dbSNP","start":140481987,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"end":140481990,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140481990,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1795292111","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140481993,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481993,"source":"dbSNP","seq_region_name":"7","id":"rs546057314","clinical_significance":[]},{"start":140481994,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140481994,"strand":1,"feature_type":"variation","id":"rs1463897299","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795292193","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140481996,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140481996,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140481999,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140481999,"clinical_significance":[],"seq_region_name":"7","id":"rs778918104"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563102206","source":"dbSNP","start":140482000,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140482000,"feature_type":"variation","strand":1},{"alleles":["A","G"],"end":140482002,"strand":1,"feature_type":"variation","start":140482002,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1795292266","clinical_significance":[]},{"start":140482002,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["AA","A"],"end":140482003,"strand":1,"feature_type":"variation","id":"rs1248178666","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795292302","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482003,"source":"dbSNP","strand":1,"feature_type":"variation","end":140482016,"alleles":["ATTTTTGTATTTTT","ATTTTT"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795292321","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482004,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140482004},{"start":140482008,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140482008,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795292334","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140482009,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482009,"source":"dbSNP","id":"rs1188343582","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs913124505","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482010,"feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140482010},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795292390","source":"dbSNP","start":140482011,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140482011,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795292403","clinical_significance":[],"strand":1,"feature_type":"variation","end":140482016,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482016,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795292422","alleles":["TAGTAG","TAG"],"end":140482021,"feature_type":"variation","strand":1,"source":"dbSNP","start":140482016,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795292442","end":140482017,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140482017,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140482019,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140482019,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1333827924"},{"clinical_significance":[],"seq_region_name":"7","id":"rs945378858","alleles":["C","G","T"],"end":140482029,"feature_type":"variation","strand":1,"source":"dbSNP","start":140482029,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795292517","clinical_significance":[],"start":140482030,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","A"],"end":140482030,"strand":1,"feature_type":"variation"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482034,"feature_type":"variation","strand":1,"end":140482034,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1396001829"},{"alleles":["A","G","T"],"end":140482037,"feature_type":"variation","strand":1,"source":"dbSNP","start":140482037,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1046456129"},{"seq_region_name":"7","id":"rs1386345724","clinical_significance":[],"start":140482042,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140482049,"alleles":["GGCCAGGC","GGC"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs564074170","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482043,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140482043},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482045,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140482045,"seq_region_name":"7","id":"rs1434414048","clinical_significance":[]},{"alleles":["G","C"],"end":140482047,"feature_type":"variation","strand":1,"source":"dbSNP","start":140482047,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795292639"},{"seq_region_name":"7","id":"rs1585511235","clinical_significance":[],"start":140482049,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140482049,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482052,"source":"dbSNP","strand":1,"feature_type":"variation","end":140482052,"alleles":["G","C"],"seq_region_name":"7","id":"rs1446004711","clinical_significance":[]},{"id":"rs1366176751","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140482053,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482053,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482055,"source":"dbSNP","strand":1,"feature_type":"variation","end":140482055,"alleles":["T","C"],"id":"rs1478844967","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1585511244","seq_region_name":"7","source":"dbSNP","start":140482056,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140482056,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs747944459","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482057,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140482057},{"start":140482059,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","G"],"end":140482059,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795292758","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585511256","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482066,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140482066},{"start":140482070,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140482070,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1252427183","clinical_significance":[]},{"clinical_significance":[],"id":"rs111506871","seq_region_name":"7","source":"dbSNP","start":140482071,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140482071,"alleles":["G","A"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140482073,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482073,"source":"dbSNP","seq_region_name":"7","id":"rs1035458779","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140482074,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482074,"source":"dbSNP","id":"rs1795292855","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585511266","feature_type":"variation","strand":1,"end":140482075,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482075},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482077,"feature_type":"variation","strand":1,"end":140482077,"alleles":["C","T"],"clinical_significance":[],"id":"rs1055211603","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140482078,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482078,"clinical_significance":[],"seq_region_name":"7","id":"rs1400755900"},{"seq_region_name":"7","id":"rs899330431","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482079,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140482079},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482081,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140482081,"seq_region_name":"7","id":"rs994979419","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140482082,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482082,"clinical_significance":[],"seq_region_name":"7","id":"rs1240069948"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482082,"source":"dbSNP","strand":1,"feature_type":"variation","end":140482091,"alleles":["GCCTAGGCCT","GCCT"],"seq_region_name":"7","id":"rs1795293004","clinical_significance":[]},{"end":140482085,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140482085,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795293025"},{"strand":1,"feature_type":"variation","end":140482086,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482086,"source":"dbSNP","id":"rs1795293042","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1337707420","alleles":["G","T"],"end":140482088,"feature_type":"variation","strand":1,"source":"dbSNP","start":140482088,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"alleles":["C","T"],"end":140482090,"strand":1,"feature_type":"variation","start":140482090,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1585511284","seq_region_name":"7","clinical_significance":[]},{"start":140482095,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","C"],"end":140482095,"strand":1,"feature_type":"variation","id":"rs1795293084","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140482099,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140482099,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795293107"},{"start":140482100,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","C"],"end":140482100,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1305331386","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482102,"source":"dbSNP","strand":1,"feature_type":"variation","end":140482109,"alleles":["TAGGATTA","TA"],"seq_region_name":"7","id":"rs1795293138","clinical_significance":[]},{"seq_region_name":"7","id":"rs1047977448","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482103,"source":"dbSNP","strand":1,"feature_type":"variation","end":140482103,"alleles":["A","C","G"]},{"seq_region_name":"7","id":"rs991183286","clinical_significance":[],"strand":1,"feature_type":"variation","end":140482119,"alleles":["GTGAG","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482115,"source":"dbSNP"},{"end":140482116,"alleles":["T","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140482116,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1386382814","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482118,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AGC","-"],"end":140482120,"id":"rs1434198496","seq_region_name":"7","clinical_significance":[]},{"end":140482120,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140482120,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs886666429","seq_region_name":"7"},{"end":140482123,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140482123,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1795293251","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1423252587","feature_type":"variation","strand":1,"end":140482126,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482126},{"id":"rs1009092966","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140482127,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482127,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1162071224","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482128,"feature_type":"variation","strand":1,"end":140482128,"alleles":["C","T"]},{"strand":1,"feature_type":"variation","end":140482129,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482129,"source":"dbSNP","seq_region_name":"7","id":"rs941862442","clinical_significance":[]},{"seq_region_name":"7","id":"rs13246753","clinical_significance":[],"start":140482130,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140482130,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs111661389","clinical_significance":[],"end":140482131,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140482131,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"id":"rs2130396467","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482132,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140482132},{"start":140482133,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","A"],"end":140482133,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1269307433","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140482146,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482146,"source":"dbSNP","id":"rs1273275407","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482153,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140482153,"id":"rs1795293522","seq_region_name":"7","clinical_significance":[]},{"id":"rs929334720","seq_region_name":"7","clinical_significance":[],"end":140482157,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140482157,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1052173183","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482168,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140482168},{"alleles":["G","A","C"],"end":140482170,"feature_type":"variation","strand":1,"source":"dbSNP","start":140482170,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1289273305"},{"clinical_significance":[],"id":"rs1795293622","seq_region_name":"7","source":"dbSNP","start":140482174,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140482174,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140482175,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482175,"source":"dbSNP","seq_region_name":"7","id":"rs996332720","clinical_significance":[]},{"alleles":["T","G"],"end":140482177,"feature_type":"variation","strand":1,"source":"dbSNP","start":140482177,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1563102238"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140482179,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482179,"clinical_significance":[],"seq_region_name":"7","id":"rs1795293686"},{"start":140482187,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140482187,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795293714","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1344448755","source":"dbSNP","start":140482191,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["GGG","GGGG"],"end":140482193,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1032728826","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482192,"source":"dbSNP","strand":1,"feature_type":"variation","end":140482192,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1205733946","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","-"],"end":140482194,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482194,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140482196,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482196,"clinical_significance":[],"seq_region_name":"7","id":"rs957446610"},{"seq_region_name":"7","id":"rs1795293849","clinical_significance":[],"alleles":["G","A"],"end":140482198,"strand":1,"feature_type":"variation","start":140482198,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1795293871","clinical_significance":[],"start":140482198,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140482199,"alleles":["GG","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795293893","feature_type":"variation","strand":1,"alleles":["CTCACT","CT"],"end":140482206,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482201},{"start":140482207,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140482207,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795293923","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1353120107","source":"dbSNP","start":140482215,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140482215,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795293965","clinical_significance":[],"alleles":["GGCTGGTCTCCAGCACCTGG","GG"],"end":140482236,"strand":1,"feature_type":"variation","start":140482217,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482221,"source":"dbSNP","strand":1,"feature_type":"variation","end":140482221,"alleles":["G","C"],"seq_region_name":"7","id":"rs890441409","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140482223,"alleles":["T","-"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482223,"clinical_significance":[],"seq_region_name":"7","id":"rs1229122175"},{"end":140482223,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140482223,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1585511330","seq_region_name":"7"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482224,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140482224,"clinical_significance":[],"id":"rs943462132","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795294574","feature_type":"variation","strand":1,"end":140482227,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482227},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482230,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140482230,"seq_region_name":"7","id":"rs1463938227","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs529353872","feature_type":"variation","strand":1,"end":140482238,"alleles":["C","G","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482238},{"alleles":["T","C"],"end":140482239,"feature_type":"variation","strand":1,"source":"dbSNP","start":140482239,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130396544"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1254086046","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482246,"feature_type":"variation","strand":1,"end":140482246,"alleles":["A","C"]},{"start":140482254,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","C"],"end":140482254,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs547595759","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795294718","clinical_significance":[],"alleles":["C","G"],"end":140482266,"strand":1,"feature_type":"variation","start":140482266,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"source":"dbSNP","start":140482267,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140482267,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795294737"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482270,"source":"dbSNP","strand":1,"feature_type":"variation","end":140482270,"alleles":["G","A"],"seq_region_name":"7","id":"rs375245065","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1386475458","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482278,"feature_type":"variation","strand":1,"end":140482278,"alleles":["A","G"]},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140482280,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482280,"source":"dbSNP","id":"rs1795294803","seq_region_name":"7","clinical_significance":[]},{"end":140482281,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140482281,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1196357288"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482291,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140482291,"seq_region_name":"7","id":"rs2130396581","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1456352187","feature_type":"variation","strand":1,"end":140482294,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482294},{"alleles":["C","T"],"end":140482295,"strand":1,"feature_type":"variation","start":140482295,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1795294866","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795294887","clinical_significance":[],"end":140482298,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140482298,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1297087183","clinical_significance":[],"strand":1,"feature_type":"variation","end":140482299,"alleles":["G","A","C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482299,"source":"dbSNP"},{"seq_region_name":"7","id":"rs551198606","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482301,"source":"dbSNP","strand":1,"feature_type":"variation","end":140482301,"alleles":["C","G","T"]},{"seq_region_name":"7","id":"rs745918022","clinical_significance":[],"end":140482302,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140482302,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482302,"feature_type":"variation","strand":1,"end":140482304,"alleles":["GGG","GGGGG"],"clinical_significance":[],"id":"rs1795294990","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140482304,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482304,"source":"dbSNP","seq_region_name":"7","id":"rs1245991695","clinical_significance":[]},{"start":140482305,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140482305,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795295048","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140482306,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482306,"source":"dbSNP","seq_region_name":"7","id":"rs1795295064","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585511353","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140482312,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482312,"source":"dbSNP"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482314,"feature_type":"variation","strand":1,"end":140482314,"alleles":["G","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1193808712"},{"seq_region_name":"7","id":"rs772249196","clinical_significance":[],"alleles":["T","C"],"end":140482318,"strand":1,"feature_type":"variation","start":140482318,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1246228739","feature_type":"variation","strand":1,"end":140482324,"alleles":["TTAATTA","TTA"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482318},{"source":"dbSNP","start":140482324,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140482324,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1042653852"},{"strand":1,"feature_type":"variation","alleles":["CCCC","CCC"],"end":140482333,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482330,"source":"dbSNP","seq_region_name":"7","id":"rs1409039016","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795295226","clinical_significance":[],"start":140482333,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140482333,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs937987066","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140482334,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482334,"source":"dbSNP"},{"alleles":["G","T"],"end":140482339,"strand":1,"feature_type":"variation","start":140482339,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs991318659","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1217765622","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140482341,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482341,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1344746634","clinical_significance":[],"alleles":["A","G"],"end":140482343,"strand":1,"feature_type":"variation","start":140482343,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"end":140482346,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140482346,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs551767572","clinical_significance":[]},{"alleles":["C","T"],"end":140482348,"feature_type":"variation","strand":1,"source":"dbSNP","start":140482348,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795295350"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795295369","source":"dbSNP","start":140482350,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140482350,"alleles":["A","T"],"feature_type":"variation","strand":1},{"id":"rs1795295392","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140482351,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482351,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482358,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140482358,"seq_region_name":"7","id":"rs1795295424","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795295450","clinical_significance":[],"alleles":["A","G"],"end":140482360,"strand":1,"feature_type":"variation","start":140482360,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1433475624","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140482361,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482361},{"end":140482368,"alleles":["TATTA","TATTATTA"],"strand":1,"feature_type":"variation","start":140482364,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1795295486","clinical_significance":[]},{"id":"rs1035787419","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140482365,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482365,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140482369,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482369,"source":"dbSNP","id":"rs1317910912","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140482370,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482370,"source":"dbSNP","seq_region_name":"7","id":"rs930829561","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795295579","end":140482371,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140482371,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795295597","alleles":["CTCT","CT"],"end":140482374,"feature_type":"variation","strand":1,"source":"dbSNP","start":140482371,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482373,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140482373,"seq_region_name":"7","id":"rs1795295622","clinical_significance":[]},{"seq_region_name":"7","id":"rs959688770","clinical_significance":[],"end":140482374,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140482374,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"source":"dbSNP","start":140482374,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140482374,"alleles":["T","TT"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795295680"},{"source":"dbSNP","start":140482375,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140482375,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs533203125","seq_region_name":"7"},{"start":140482384,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140482384,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795295739","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795295770","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140482385,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482385},{"clinical_significance":[],"seq_region_name":"7","id":"rs550338387","feature_type":"variation","strand":1,"alleles":["TTTTT","TTTT"],"end":140482395,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482391},{"alleles":["C","T"],"end":140482396,"feature_type":"variation","strand":1,"source":"dbSNP","start":140482396,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1178331943"},{"source":"dbSNP","start":140482399,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140482399,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs2130396709","seq_region_name":"7"},{"end":140482400,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140482400,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1412613254"},{"alleles":["G","A"],"end":140482401,"feature_type":"variation","strand":1,"source":"dbSNP","start":140482401,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795295836","seq_region_name":"7"},{"start":140482404,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140482404,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1022668563","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482409,"source":"dbSNP","strand":1,"feature_type":"variation","end":140482409,"alleles":["G","A"],"id":"rs552091129","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs139676958","clinical_significance":[],"alleles":["C","A","T"],"end":140482412,"strand":1,"feature_type":"variation","start":140482412,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs7799539","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482413,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140482413},{"seq_region_name":"7","id":"rs1245271785","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482419,"source":"dbSNP","strand":1,"feature_type":"variation","end":140482419,"alleles":["T","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795296176","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140482421,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482421},{"end":140482422,"alleles":["G","A","C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140482422,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs188317398"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795296250","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482423,"feature_type":"variation","strand":1,"end":140482423,"alleles":["T","A"]},{"feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140482424,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482424,"clinical_significance":[],"seq_region_name":"7","id":"rs987392671"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795296303","feature_type":"variation","strand":1,"end":140482429,"alleles":["C","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482429},{"clinical_significance":[],"seq_region_name":"7","id":"rs911914622","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140482432,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482432},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482433,"source":"dbSNP","strand":1,"feature_type":"variation","end":140482433,"alleles":["G","A"],"seq_region_name":"7","id":"rs78284791","clinical_significance":[]},{"seq_region_name":"7","id":"rs1294785275","clinical_significance":[],"start":140482434,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140482434,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482440,"feature_type":"variation","strand":1,"end":140482440,"alleles":["G","A"],"clinical_significance":[],"id":"rs1795296498","seq_region_name":"7"},{"seq_region_name":"7","id":"rs773012592","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482442,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140482442},{"id":"rs1226940964","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["AATCAGCCTATTAATCA","AATCA"],"end":140482461,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482445,"source":"dbSNP"},{"source":"dbSNP","start":140482447,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140482447,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1266517725","seq_region_name":"7"},{"id":"rs1795296626","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140482449,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482449,"source":"dbSNP"},{"clinical_significance":[],"id":"rs566859032","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482451,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140482451},{"seq_region_name":"7","id":"rs1795296670","clinical_significance":[],"start":140482452,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140482452,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"start":140482454,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140482454,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795296696","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795296738","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482459,"feature_type":"variation","strand":1,"end":140482459,"alleles":["T","C"]},{"strand":1,"feature_type":"variation","end":140482466,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482466,"source":"dbSNP","seq_region_name":"7","id":"rs1795296763","clinical_significance":[]},{"end":140482467,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140482467,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs535507540","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140482468,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482468,"clinical_significance":[],"seq_region_name":"7","id":"rs7777768"},{"clinical_significance":[],"seq_region_name":"7","id":"rs377117974","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482468,"feature_type":"variation","strand":1,"end":140482469,"alleles":["CC","TG"]},{"seq_region_name":"7","id":"rs7777769","clinical_significance":[],"strand":1,"feature_type":"variation","end":140482469,"alleles":["C","A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482469,"source":"dbSNP"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482469,"feature_type":"variation","strand":1,"alleles":["CC","TG"],"end":140482470,"clinical_significance":[],"id":"rs1554452348","seq_region_name":"7"},{"source":"dbSNP","start":140482470,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140482470,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1289536355"},{"feature_type":"variation","strand":1,"end":140482471,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482471,"clinical_significance":[],"seq_region_name":"7","id":"rs946882299"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1368553526","alleles":["T","A","C","G"],"end":140482473,"feature_type":"variation","strand":1,"source":"dbSNP","start":140482473,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795297193","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140482477,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482477,"source":"dbSNP"},{"alleles":["CCCAACAC","C"],"end":140482484,"strand":1,"feature_type":"variation","start":140482477,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1042927232","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585511447","end":140482478,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140482478,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482489,"source":"dbSNP","strand":1,"feature_type":"variation","end":140482489,"alleles":["A","G"],"seq_region_name":"7","id":"rs1183889616","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140482494,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482494,"source":"dbSNP","id":"rs1387139597","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482495,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140482495,"seq_region_name":"7","id":"rs1249055672","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs892910609","alleles":["G","T"],"end":140482496,"feature_type":"variation","strand":1,"source":"dbSNP","start":140482496,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"start":140482499,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140482499,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795297371","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482500,"feature_type":"variation","strand":1,"end":140482500,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795297398"},{"strand":1,"feature_type":"variation","end":140482503,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482503,"source":"dbSNP","seq_region_name":"7","id":"rs560029536","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795297460","end":140482514,"alleles":["AACAACA","AACA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140482508,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795297481","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140482509,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482509,"source":"dbSNP"},{"alleles":["A","G"],"end":140482511,"strand":1,"feature_type":"variation","start":140482511,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1233841190","clinical_significance":[]},{"source":"dbSNP","start":140482520,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140482520,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1471965125"},{"id":"rs1795297553","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482525,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140482525},{"clinical_significance":[],"id":"rs1009976420","seq_region_name":"7","source":"dbSNP","start":140482530,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140482530,"alleles":["C","T"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140482536,"alleles":["G","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482536,"clinical_significance":[],"seq_region_name":"7","id":"rs1795297613"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795297633","source":"dbSNP","start":140482537,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140482537,"feature_type":"variation","strand":1},{"id":"rs368476181","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140482539,"alleles":["A","C","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482539,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1482363668","clinical_significance":[],"strand":1,"feature_type":"variation","end":140482541,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482541,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563102310","end":140482542,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140482542,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1223868203","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482544,"feature_type":"variation","strand":1,"end":140482544,"alleles":["A","G"]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482544,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","-"],"end":140482544,"id":"rs1456283609","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1359597999","feature_type":"variation","strand":1,"end":140482545,"alleles":["C","A","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482545},{"clinical_significance":[],"seq_region_name":"7","id":"rs1056711730","feature_type":"variation","strand":1,"end":140482548,"alleles":["C","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482548},{"seq_region_name":"7","id":"rs1795297848","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482553,"source":"dbSNP","strand":1,"feature_type":"variation","end":140482560,"alleles":["TAACTAAC","TAAC"]},{"clinical_significance":[],"id":"rs1226276869","seq_region_name":"7","alleles":["A","T"],"end":140482555,"feature_type":"variation","strand":1,"source":"dbSNP","start":140482555,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795297907","clinical_significance":[],"start":140482556,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140482556,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs774040890","clinical_significance":[],"alleles":["A","G"],"end":140482558,"strand":1,"feature_type":"variation","start":140482558,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1795297973","clinical_significance":[],"start":140482560,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140482560,"strand":1,"feature_type":"variation"},{"id":"rs1795298000","seq_region_name":"7","clinical_significance":[],"start":140482561,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140482561,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140482563,"alleles":["T","-"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482563,"clinical_significance":[],"id":"rs1430709565","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140482564,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482564,"clinical_significance":[],"seq_region_name":"7","id":"rs971217434"},{"seq_region_name":"7","id":"rs981359361","clinical_significance":[],"end":140482569,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140482569,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140482570,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482570,"source":"dbSNP","seq_region_name":"7","id":"rs1022681581","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482578,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140482578,"id":"rs1409324934","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","C"],"end":140482582,"feature_type":"variation","strand":1,"source":"dbSNP","start":140482582,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130396951"},{"end":140482585,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140482585,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1313474723","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140482589,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482589,"clinical_significance":[],"id":"rs1795298231","seq_region_name":"7"},{"id":"rs1795298256","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140482596,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482596,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs7785094","source":"dbSNP","start":140482602,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140482602,"alleles":["A","G"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140482604,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140482604,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795298375"},{"seq_region_name":"7","id":"rs1795298398","clinical_significance":[],"end":140482605,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140482605,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482606,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140482606,"seq_region_name":"7","id":"rs1162711537","clinical_significance":[]},{"source":"dbSNP","start":140482608,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140482608,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1405001090"},{"source":"dbSNP","start":140482609,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140482609,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1243163521"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482610,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140482610,"seq_region_name":"7","id":"rs1179165892","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482611,"source":"dbSNP","strand":1,"feature_type":"variation","end":140482611,"alleles":["T","C"],"seq_region_name":"7","id":"rs1795298487","clinical_significance":[]},{"seq_region_name":"7","id":"rs1471849978","clinical_significance":[],"strand":1,"feature_type":"variation","end":140482612,"alleles":["TT","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482611,"source":"dbSNP"},{"id":"rs1795298595","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482617,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140482617},{"seq_region_name":"7","id":"rs1251520043","clinical_significance":[],"end":140482619,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140482619,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"id":"rs1795298658","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140482620,"strand":1,"feature_type":"variation","start":140482620,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"source":"dbSNP","start":140482622,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140482622,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs375494486","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1490968970","clinical_significance":[],"alleles":["G","A"],"end":140482623,"strand":1,"feature_type":"variation","start":140482623,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"id":"rs2130397026","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140482625,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482625},{"source":"dbSNP","start":140482626,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140482626,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1026592918","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1218652679","source":"dbSNP","start":140482628,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140482628,"alleles":["G","A"],"feature_type":"variation","strand":1},{"end":140482629,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140482629,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs990810879","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795298877","source":"dbSNP","start":140482631,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140482631,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140482634,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482634,"clinical_significance":[],"id":"rs575891358","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1229825423","feature_type":"variation","strand":1,"end":140482635,"alleles":["G","A","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482635},{"clinical_significance":[],"seq_region_name":"7","id":"rs1287441287","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482637,"feature_type":"variation","strand":1,"end":140482637,"alleles":["C","A","T"]},{"clinical_significance":[],"id":"rs1405508308","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482638,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140482638},{"seq_region_name":"7","id":"rs930764356","clinical_significance":[],"start":140482639,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A","C"],"end":140482639,"strand":1,"feature_type":"variation"},{"start":140482640,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140482640,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585511523","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs983498367","alleles":["C","T"],"end":140482645,"feature_type":"variation","strand":1,"source":"dbSNP","start":140482645,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140482646,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482646,"source":"dbSNP","seq_region_name":"7","id":"rs1291866159","clinical_significance":[]},{"id":"rs1206910649","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482648,"source":"dbSNP","strand":1,"feature_type":"variation","end":140482648,"alleles":["G","A"]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140482649,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482649,"clinical_significance":[],"id":"rs950571912","seq_region_name":"7"},{"seq_region_name":"7","id":"rs908055376","clinical_significance":[],"end":140482653,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140482653,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"start":140482654,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140482654,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795299215","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130397076","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140482656,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482656,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1482501071","clinical_significance":[],"start":140482659,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140482659,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482660,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140482660,"id":"rs1280553983","seq_region_name":"7","clinical_significance":[]},{"end":140482661,"alleles":["C","-"],"strand":1,"feature_type":"variation","start":140482661,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1411733681","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140482662,"alleles":["A","C","G","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482662,"clinical_significance":[],"seq_region_name":"7","id":"rs1200556204"},{"end":140482663,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140482663,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1265958548"},{"clinical_significance":[],"id":"rs911771796","seq_region_name":"7","end":140482667,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140482667,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482671,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140482671,"seq_region_name":"7","id":"rs368494374","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482672,"feature_type":"variation","strand":1,"end":140482672,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1422054781"},{"seq_region_name":"7","id":"rs1795299553","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["GGATTGCATGAGGTCAGGA","GGATTGCATGAGGTCAGGATTGCATGAGGTCAGGA"],"end":140482690,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482672,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795299576","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140482676,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482676,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1041039273","clinical_significance":[],"start":140482679,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140482679,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795299636","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482680,"feature_type":"variation","strand":1,"end":140482680,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1563102354","clinical_significance":[],"end":140482681,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140482681,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482683,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140482683,"clinical_significance":[],"seq_region_name":"7","id":"rs1795299685"},{"alleles":["G","A","C"],"end":140482684,"strand":1,"feature_type":"variation","start":140482684,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1186737523","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482686,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140482686,"clinical_significance":[],"seq_region_name":"7","id":"rs915347792"},{"end":140482694,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140482694,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs900730381","seq_region_name":"7"},{"clinical_significance":[],"id":"rs144364759","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482695,"feature_type":"variation","strand":1,"end":140482695,"alleles":["G","A"]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140482697,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482697,"clinical_significance":[],"id":"rs1042462169","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795299979","feature_type":"variation","strand":1,"alleles":["A","T"],"end":140482701,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482701},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482705,"feature_type":"variation","strand":1,"end":140482705,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795300009"},{"seq_region_name":"7","id":"rs146613136","clinical_significance":[],"strand":1,"feature_type":"variation","end":140482706,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482706,"source":"dbSNP"},{"id":"rs113247159","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482714,"source":"dbSNP","strand":1,"feature_type":"variation","end":140482714,"alleles":["T","A","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795300116","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140482715,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482715},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795300167","feature_type":"variation","strand":1,"end":140482721,"alleles":["AAAAA","AAAA"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482717},{"clinical_significance":[],"id":"rs1795300194","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482719,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140482719},{"seq_region_name":"7","id":"rs1585511573","clinical_significance":[],"end":140482721,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140482721,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"end":140482722,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140482722,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795300253"},{"id":"rs1010027314","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140482726,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482726,"source":"dbSNP"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482727,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140482727,"clinical_significance":[],"seq_region_name":"7","id":"rs1795300314"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585511575","source":"dbSNP","start":140482728,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140482728,"alleles":["T","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1303501926","alleles":["C","T"],"end":140482731,"feature_type":"variation","strand":1,"source":"dbSNP","start":140482731,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"alleles":["AAAAA","AAAA","AAAAAA"],"end":140482740,"strand":1,"feature_type":"variation","start":140482736,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1404431209","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140482740,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482740,"source":"dbSNP","id":"rs1394858457","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482743,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140482743,"clinical_significance":[],"seq_region_name":"7","id":"rs1312601535"},{"alleles":["A","G"],"end":140482745,"feature_type":"variation","strand":1,"source":"dbSNP","start":140482745,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs559629210"},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140482748,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482748,"clinical_significance":[],"id":"rs2130397199","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482750,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140482750,"seq_region_name":"7","id":"rs1433200984","clinical_significance":[]},{"seq_region_name":"7","id":"rs1388091805","clinical_significance":[],"start":140482752,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140482752,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1020006002","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482753,"feature_type":"variation","strand":1,"end":140482753,"alleles":["C","G","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795300634","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140482755,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482755},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482757,"feature_type":"variation","strand":1,"end":140482757,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs533355627"},{"clinical_significance":[],"id":"rs1467951122","seq_region_name":"7","source":"dbSNP","start":140482759,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140482759,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1746853054","clinical_significance":[],"end":140482760,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140482760,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"alleles":["C","T"],"end":140482766,"strand":1,"feature_type":"variation","start":140482766,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs551755460","clinical_significance":[]},{"clinical_significance":[],"id":"rs1002677268","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482767,"feature_type":"variation","strand":1,"end":140482767,"alleles":["G","A","C","T"]},{"start":140482767,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["GTGTGT","GTGT"],"end":140482772,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1176023002","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs563684573","source":"dbSNP","start":140482775,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140482775,"alleles":["G","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1585511599","clinical_significance":[],"start":140482779,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140482779,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1295794672","clinical_significance":[],"start":140482780,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140482780,"strand":1,"feature_type":"variation"},{"id":"rs1795300933","seq_region_name":"7","clinical_significance":[],"start":140482783,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","T"],"end":140482783,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1341036863","alleles":["C","G"],"end":140482785,"feature_type":"variation","strand":1,"source":"dbSNP","start":140482785,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"end":140482791,"alleles":["CC","C"],"strand":1,"feature_type":"variation","start":140482790,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1795300990","clinical_significance":[]},{"clinical_significance":[],"id":"rs2130397266","seq_region_name":"7","end":140482791,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140482791,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"end":140482795,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140482795,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1044061435","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1257307620","clinical_significance":[],"start":140482798,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["-","ATAT"],"end":140482797,"strand":1,"feature_type":"variation"},{"alleles":["G","C"],"end":140482798,"feature_type":"variation","strand":1,"source":"dbSNP","start":140482798,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs898819792"},{"source":"dbSNP","start":140482799,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140482798,"alleles":["-","AGCTTGCCCTCCCCGT"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1481977310"},{"start":140482801,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140482801,"alleles":["A","G"],"strand":1,"feature_type":"variation","id":"rs1180591827","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795301167","feature_type":"variation","strand":1,"alleles":["A","-"],"end":140482801,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482801},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795301204","alleles":["-","GGGTTGGGATCATC"],"end":140482802,"feature_type":"variation","strand":1,"source":"dbSNP","start":140482803,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140482803,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482803,"source":"dbSNP","seq_region_name":"7","id":"rs531197953","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs548564112","source":"dbSNP","start":140482804,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140482804,"alleles":["C","A","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795301307","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482805,"feature_type":"variation","strand":1,"end":140482804,"alleles":["-","TCT"]},{"feature_type":"variation","strand":1,"end":140482805,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482805,"clinical_significance":[],"seq_region_name":"7","id":"rs1026060933"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140482807,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482807,"clinical_significance":[],"id":"rs958671295","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795301396","clinical_significance":[],"strand":1,"feature_type":"variation","end":140482807,"alleles":["-","GTTCTCCCTGTGCACATTAATAAATGTGTATGCCTTTTCATCAATA"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482808,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1232486389","clinical_significance":[],"start":140482808,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140482808,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs995814769","seq_region_name":"7","source":"dbSNP","start":140482811,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140482811,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["T","-"],"end":140482811,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482811,"clinical_significance":[],"id":"rs1795301484","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140482813,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482813,"source":"dbSNP","seq_region_name":"7","id":"rs1585511623","clinical_significance":[]},{"seq_region_name":"7","id":"rs1299919701","clinical_significance":[],"start":140482817,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140482817,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795301651","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140482821,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482821},{"alleles":["T","A"],"end":140482822,"strand":1,"feature_type":"variation","start":140482822,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1226357564","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs886273238","clinical_significance":[],"end":140482827,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140482827,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"alleles":["A","G"],"end":140482831,"strand":1,"feature_type":"variation","start":140482831,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1795301735","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140482832,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482832,"source":"dbSNP","seq_region_name":"7","id":"rs1389252458","clinical_significance":[]},{"id":"rs1316051767","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482832,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["ACTAC","AC"],"end":140482836},{"strand":1,"feature_type":"variation","end":140482833,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482833,"source":"dbSNP","seq_region_name":"7","id":"rs1397974038","clinical_significance":[]},{"id":"rs1585511633","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140482836,"strand":1,"feature_type":"variation","start":140482836,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482837,"feature_type":"variation","strand":1,"end":140482837,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1008696703"},{"alleles":["T","A"],"end":140482841,"feature_type":"variation","strand":1,"source":"dbSNP","start":140482841,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795301903","seq_region_name":"7"},{"start":140482843,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140482843,"alleles":["C","A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1302581188","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795301968","clinical_significance":[],"start":140482846,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","G"],"end":140482846,"strand":1,"feature_type":"variation"},{"end":140482850,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140482850,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs545409663","clinical_significance":[]},{"alleles":["A","G"],"end":140482851,"feature_type":"variation","strand":1,"source":"dbSNP","start":140482851,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs191906683"},{"id":"rs1795302073","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482857,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140482857},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482859,"source":"dbSNP","strand":1,"feature_type":"variation","end":140482859,"alleles":["A","G"],"seq_region_name":"7","id":"rs1795302097","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1167258605","alleles":["A","C"],"end":140482863,"feature_type":"variation","strand":1,"source":"dbSNP","start":140482863,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs757742257","clinical_significance":[],"start":140482872,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","A","T"],"end":140482872,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140482873,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482873,"source":"dbSNP","seq_region_name":"7","id":"rs983509753","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140482875,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482875,"clinical_significance":[],"seq_region_name":"7","id":"rs1795302535"},{"strand":1,"feature_type":"variation","end":140482876,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482876,"source":"dbSNP","id":"rs867614035","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1425148441","clinical_significance":[],"start":140482877,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140482877,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1253848795","clinical_significance":[],"alleles":["T","C"],"end":140482878,"strand":1,"feature_type":"variation","start":140482878,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"id":"rs1795302731","seq_region_name":"7","clinical_significance":[],"start":140482880,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140482880,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs966200141","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482885,"source":"dbSNP","strand":1,"feature_type":"variation","end":140482885,"alleles":["T","G"]},{"alleles":["C","G"],"end":140482886,"feature_type":"variation","strand":1,"source":"dbSNP","start":140482886,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795302784"},{"start":140482888,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","A","T"],"end":140482888,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1302296390","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795302857","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482889,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140482889},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795302881","feature_type":"variation","strand":1,"end":140482892,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482892},{"seq_region_name":"7","id":"rs1390048689","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482896,"source":"dbSNP","strand":1,"feature_type":"variation","end":140482896,"alleles":["A","C"]},{"seq_region_name":"7","id":"rs1276755723","clinical_significance":[],"end":140482898,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140482898,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"id":"rs1480832145","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482898,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CCC","CC"],"end":140482900},{"clinical_significance":[],"id":"rs1022335080","seq_region_name":"7","source":"dbSNP","start":140482900,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140482900,"alleles":["C","T"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140482902,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482902,"source":"dbSNP","seq_region_name":"7","id":"rs1795303065","clinical_significance":[]},{"start":140482904,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140482904,"alleles":["A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795303088","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs976302564","end":140482905,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140482905,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795303151","feature_type":"variation","strand":1,"end":140482907,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482907},{"alleles":["A","G"],"end":140482910,"feature_type":"variation","strand":1,"source":"dbSNP","start":140482910,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs968071120"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795303217","alleles":["A","G"],"end":140482912,"feature_type":"variation","strand":1,"source":"dbSNP","start":140482912,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140482916,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140482916,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs922082295","seq_region_name":"7"},{"clinical_significance":[],"id":"rs932284609","seq_region_name":"7","feature_type":"variation","strand":1,"end":140482921,"alleles":["C","G","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482921},{"clinical_significance":[],"seq_region_name":"7","id":"rs1312464569","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482922,"feature_type":"variation","strand":1,"end":140482922,"alleles":["G","A"]},{"clinical_significance":[],"id":"rs1364907636","seq_region_name":"7","source":"dbSNP","start":140482923,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140482923,"alleles":["G","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs567828065","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482925,"source":"dbSNP","strand":1,"feature_type":"variation","end":140482925,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs759202847","clinical_significance":[],"end":140482926,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140482926,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"alleles":["G","A"],"end":140482927,"strand":1,"feature_type":"variation","start":140482927,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1306774392","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140482932,"alleles":["C","G","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482932,"clinical_significance":[],"seq_region_name":"7","id":"rs1429643686"},{"clinical_significance":[],"id":"rs1055112893","seq_region_name":"7","source":"dbSNP","start":140482933,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140482933,"alleles":["G","A"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140482934,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140482934,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795303555"},{"seq_region_name":"7","id":"rs914243766","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482935,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G","T"],"end":140482935},{"clinical_significance":[],"id":"rs945660085","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140482940,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482940},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140482944,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482944,"clinical_significance":[],"id":"rs1459137270","seq_region_name":"7"},{"end":140482946,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140482946,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1041499078","seq_region_name":"7","clinical_significance":[]},{"end":140482947,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140482947,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585511703"},{"seq_region_name":"7","id":"rs1795303738","clinical_significance":[],"strand":1,"feature_type":"variation","end":140482952,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482952,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482954,"source":"dbSNP","strand":1,"feature_type":"variation","end":140482954,"alleles":["G","T"],"seq_region_name":"7","id":"rs1186380824","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1472822661","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482956,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140482956},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482959,"source":"dbSNP","strand":1,"feature_type":"variation","end":140482959,"alleles":["G","A"],"seq_region_name":"7","id":"rs1253662502","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140482960,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482960,"clinical_significance":[],"id":"rs1310036843","seq_region_name":"7"},{"id":"rs1179962643","seq_region_name":"7","clinical_significance":[],"start":140482964,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","G"],"end":140482964,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1482658761","clinical_significance":[],"start":140482965,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140482965,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140482966,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482966,"clinical_significance":[],"seq_region_name":"7","id":"rs767832130"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482967,"source":"dbSNP","strand":1,"feature_type":"variation","end":140482967,"alleles":["G","A","T"],"id":"rs1211644416","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482972,"feature_type":"variation","strand":1,"end":140482972,"alleles":["A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs924011578"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140482974,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140482974,"seq_region_name":"7","id":"rs906926059","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1240003055","feature_type":"variation","strand":1,"end":140482979,"alleles":["T","A","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482979},{"end":140482985,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140482985,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795304032","seq_region_name":"7"},{"end":140482991,"alleles":["AAAAA","AAAAAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140482987,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795304061"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482991,"feature_type":"variation","strand":1,"end":140482991,"alleles":["A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs939524812"},{"start":140482993,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140482993,"alleles":["T","A"],"strand":1,"feature_type":"variation","id":"rs1286807905","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130397499","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482994,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140482994},{"start":140482998,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140482998,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795304372","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140482999,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140482999,"clinical_significance":[],"id":"rs1795304406","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1409774288","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483003,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140483003},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795304425","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483009,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140483009},{"end":140483010,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140483010,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs992261126","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140483012,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140483012,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1331145712"},{"id":"rs1003015796","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483013,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140483013},{"seq_region_name":"7","id":"rs1206733773","clinical_significance":[],"alleles":["T","C"],"end":140483014,"strand":1,"feature_type":"variation","start":140483014,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1055659628","clinical_significance":[],"strand":1,"feature_type":"variation","end":140483017,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483017,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483018,"source":"dbSNP","strand":1,"feature_type":"variation","end":140483018,"alleles":["G","A","T"],"seq_region_name":"7","id":"rs894299660","clinical_significance":[]},{"seq_region_name":"7","id":"rs1413931015","clinical_significance":[],"end":140483019,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140483019,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"start":140483021,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140483021,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs563773117","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs141076625","clinical_significance":[],"alleles":["G","A"],"end":140483022,"strand":1,"feature_type":"variation","start":140483022,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140483023,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483023,"clinical_significance":[],"seq_region_name":"7","id":"rs1247286334"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1269773225","feature_type":"variation","strand":1,"end":140483026,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483026},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140483028,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483028,"clinical_significance":[],"id":"rs547460791","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483029,"source":"dbSNP","strand":1,"feature_type":"variation","end":140483029,"alleles":["G","A"],"seq_region_name":"7","id":"rs1449990861","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795304921","clinical_significance":[],"start":140483032,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140483032,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"start":140483036,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140483036,"alleles":["C","A"],"strand":1,"feature_type":"variation","id":"rs1431605894","seq_region_name":"7","clinical_significance":[]},{"start":140483041,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140483041,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1266723990","clinical_significance":[]},{"id":"rs1795304993","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140483045,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483045,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1175813230","seq_region_name":"7","source":"dbSNP","start":140483046,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140483046,"alleles":["G","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1004816655","alleles":["G","T"],"end":140483047,"feature_type":"variation","strand":1,"source":"dbSNP","start":140483047,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140483049,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483049,"clinical_significance":[],"seq_region_name":"7","id":"rs1209634058"},{"clinical_significance":[],"id":"rs1412712994","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483050,"feature_type":"variation","strand":1,"end":140483050,"alleles":["G","A"]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483051,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140483051,"clinical_significance":[],"seq_region_name":"7","id":"rs916727085"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483052,"feature_type":"variation","strand":1,"end":140483052,"alleles":["G","A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1459337920"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483054,"feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140483054,"clinical_significance":[],"seq_region_name":"7","id":"rs182886667"},{"source":"dbSNP","start":140483055,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140483055,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795305181"},{"source":"dbSNP","start":140483056,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140483056,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1277165331","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1795305238","seq_region_name":"7","source":"dbSNP","start":140483059,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140483059,"alleles":["G","A"],"feature_type":"variation","strand":1},{"start":140483064,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140483064,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs966128928","clinical_significance":[]},{"id":"rs1795305356","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140483065,"strand":1,"feature_type":"variation","start":140483065,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"id":"rs1328877407","seq_region_name":"7","clinical_significance":[],"start":140483069,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","C"],"end":140483069,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585511787","source":"dbSNP","start":140483070,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140483070,"feature_type":"variation","strand":1},{"end":140483071,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140483071,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs898873817"},{"clinical_significance":[],"seq_region_name":"7","id":"rs539156464","end":140483073,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140483073,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1435378419","end":140483074,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140483074,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483078,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140483078,"clinical_significance":[],"seq_region_name":"7","id":"rs2130397596"},{"source":"dbSNP","start":140483079,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140483079,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795305463","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1390302787","clinical_significance":[],"alleles":["T","C"],"end":140483080,"strand":1,"feature_type":"variation","start":140483080,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483081,"source":"dbSNP","strand":1,"feature_type":"variation","end":140483081,"alleles":["G","A"],"id":"rs1318117050","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140483084,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483084,"clinical_significance":[],"seq_region_name":"7","id":"rs930287244"},{"seq_region_name":"7","id":"rs976566728","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140483085,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483085,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1174288568","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483089,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140483089},{"source":"dbSNP","start":140483094,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140483094,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs922162756"},{"source":"dbSNP","start":140483096,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140483096,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795305622"},{"seq_region_name":"7","id":"rs1795305638","clinical_significance":[],"start":140483097,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140483097,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1047941821","seq_region_name":"7","alleles":["A","G"],"end":140483098,"feature_type":"variation","strand":1,"source":"dbSNP","start":140483098,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"start":140483100,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140483100,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs953631058","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140483101,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483101,"clinical_significance":[],"id":"rs1795305686","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795305708","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483104,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140483104},{"alleles":["AA","-"],"end":140483105,"feature_type":"variation","strand":1,"source":"dbSNP","start":140483104,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795305721"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795305735","source":"dbSNP","start":140483105,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140483105,"alleles":["A","C"],"feature_type":"variation","strand":1},{"end":140483106,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140483106,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795305746"},{"seq_region_name":"7","id":"rs1377165025","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140483107,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483107,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795305769","end":140483107,"alleles":["C","CAC"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140483107,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483108,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140483108,"clinical_significance":[],"seq_region_name":"7","id":"rs1365072188"},{"alleles":["G","A"],"end":140483112,"strand":1,"feature_type":"variation","start":140483112,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1795305801","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140483114,"alleles":["A","C","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483114,"clinical_significance":[],"seq_region_name":"7","id":"rs557295718"},{"source":"dbSNP","start":140483115,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140483115,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs990424292"},{"seq_region_name":"7","id":"rs1288510148","clinical_significance":[],"start":140483117,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140483117,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795305879","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483119,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140483119},{"clinical_significance":[],"seq_region_name":"7","id":"rs34526173","source":"dbSNP","start":140483119,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140483120,"alleles":["AA","AAA"],"feature_type":"variation","strand":1},{"end":140483120,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140483120,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs914798086","clinical_significance":[]},{"end":140483121,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140483121,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs945710758","clinical_significance":[]},{"id":"rs1041424664","seq_region_name":"7","clinical_significance":[],"start":140483124,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140483124,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140483138,"alleles":["GAGTGAG","GAG"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483132,"clinical_significance":[],"seq_region_name":"7","id":"rs1795305952"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483133,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140483133,"seq_region_name":"7","id":"rs928270614","clinical_significance":[]},{"id":"rs1408598801","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483134,"source":"dbSNP","strand":1,"feature_type":"variation","end":140483134,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1009165606","clinical_significance":[],"strand":1,"feature_type":"variation","end":140483136,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483136,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140483138,"alleles":["G","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483138,"clinical_significance":[],"seq_region_name":"7","id":"rs1226545869"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483140,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140483140,"seq_region_name":"7","id":"rs1795306075","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795306091","clinical_significance":[],"end":140483148,"alleles":["CTCTGTCTC","CTC"],"strand":1,"feature_type":"variation","start":140483140,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"alleles":["C","G"],"end":140483142,"strand":1,"feature_type":"variation","start":140483142,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs2130397686","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795306143","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483143,"feature_type":"variation","strand":1,"alleles":["T","TTT"],"end":140483143},{"seq_region_name":"7","id":"rs1228587726","clinical_significance":[],"end":140483149,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140483149,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs938477596","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483150,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140483150},{"id":"rs1295011969","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483151,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AAATAAATAAAT","AAATAAAT"],"end":140483162},{"alleles":["TAAATTAA","TAA"],"end":140483165,"strand":1,"feature_type":"variation","start":140483158,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1433866160","clinical_significance":[]},{"end":140483159,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140483159,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs374831003","clinical_significance":[]},{"seq_region_name":"7","id":"rs996129741","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483160,"source":"dbSNP","strand":1,"feature_type":"variation","end":140483160,"alleles":["A","C","G"]},{"seq_region_name":"7","id":"rs796521141","clinical_significance":[],"alleles":["AATTAATTAATTAA","AATTAATTAA"],"end":140483173,"strand":1,"feature_type":"variation","start":140483160,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"feature_type":"variation","strand":1,"end":140483162,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483162,"clinical_significance":[],"seq_region_name":"7","id":"rs1169141207"},{"clinical_significance":[],"seq_region_name":"7","id":"rs758339437","source":"dbSNP","start":140483163,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140483163,"alleles":["T","A","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795306422","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483164,"feature_type":"variation","strand":1,"alleles":["AA","A"],"end":140483165},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140483173,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483173,"clinical_significance":[],"id":"rs1388363532","seq_region_name":"7"},{"end":140483176,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140483176,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1795306452","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140483185,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483185,"clinical_significance":[],"seq_region_name":"7","id":"rs6971596"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1473219010","feature_type":"variation","strand":1,"end":140483198,"alleles":["C","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483198},{"clinical_significance":[],"id":"rs1795306560","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140483199,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483199},{"seq_region_name":"7","id":"rs2130397741","clinical_significance":[],"end":140483200,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140483200,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1239592204","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483201,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140483201},{"start":140483204,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","A"],"end":140483204,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1185781449","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1048318070","feature_type":"variation","strand":1,"end":140483205,"alleles":["A","C","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483205},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140483209,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483209,"clinical_significance":[],"seq_region_name":"7","id":"rs1223522367"},{"clinical_significance":[],"id":"rs1276048805","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483211,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140483211},{"seq_region_name":"7","id":"rs1795306656","clinical_significance":[],"start":140483216,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140483216,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs77283328","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483217,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140483217},{"feature_type":"variation","strand":1,"alleles":["AAAAAAAA","AAAAAA","AAAAAAA","AAAAAAAAA","AAAAAAAAAAAA"],"end":140483224,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483217,"clinical_significance":[],"seq_region_name":"7","id":"rs140569384"},{"seq_region_name":"7","id":"rs112424242","clinical_significance":[],"start":140483218,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140483218,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140483218,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140483221,"alleles":["AAAA","AAAAGAAAA"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs768004430"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1554452450","alleles":["-","G"],"end":140483218,"feature_type":"variation","strand":1,"source":"dbSNP","start":140483219,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs34649745","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["AAA","AAAGAAA","AAAGAAAAAACAAAAAAGAAA"],"end":140483221,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483219,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1487630826","clinical_significance":[],"end":140483221,"alleles":["AA","AAGAA"],"strand":1,"feature_type":"variation","start":140483220,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"id":"rs1198951437","seq_region_name":"7","feature_type":"variation","strand":1,"end":140483221,"alleles":["A","AGA"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483221},{"clinical_significance":[],"seq_region_name":"7","id":"rs1339644283","source":"dbSNP","start":140483221,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["AAAACAAA","AAA"],"end":140483228,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140483222,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["-","G"],"end":140483221,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs77172386","seq_region_name":"7"},{"clinical_significance":[],"id":"rs11972850","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483222,"feature_type":"variation","strand":1,"end":140483222,"alleles":["A","G"]},{"end":140483228,"alleles":["AAACAAA","AAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140483222,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1308596569","seq_region_name":"7"},{"alleles":["A","C"],"end":140483224,"feature_type":"variation","strand":1,"source":"dbSNP","start":140483224,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1731184518"},{"id":"rs1369783454","seq_region_name":"7","clinical_significance":[],"start":140483225,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140483225,"alleles":["C","-"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1252690175","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483226,"source":"dbSNP","strand":1,"feature_type":"variation","end":140483231,"alleles":["AAATAA","AA"]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483229,"source":"dbSNP","strand":1,"feature_type":"variation","end":140483229,"alleles":["T","C"],"seq_region_name":"7","id":"rs1795307416","clinical_significance":[]},{"seq_region_name":"7","id":"rs1368812875","clinical_significance":[],"strand":1,"feature_type":"variation","end":140483230,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483230,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs887049207","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483232,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140483232},{"source":"dbSNP","start":140483233,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140483233,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1436805007"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483235,"source":"dbSNP","strand":1,"feature_type":"variation","end":140483235,"alleles":["A","G"],"id":"rs747985181","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795307563","source":"dbSNP","start":140483248,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140483248,"alleles":["G","C"],"feature_type":"variation","strand":1},{"start":140483249,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140483249,"strand":1,"feature_type":"variation","id":"rs529093026","seq_region_name":"7","clinical_significance":[]},{"id":"rs1585511933","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140483250,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483250,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs150281981","end":140483252,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140483252,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"alleles":["C","G"],"end":140483259,"strand":1,"feature_type":"variation","start":140483259,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1472703412","clinical_significance":[]},{"alleles":["A","G"],"end":140483264,"strand":1,"feature_type":"variation","start":140483264,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1252953127","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795307753","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140483271,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483271},{"clinical_significance":[],"id":"rs888333527","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483275,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140483275},{"source":"dbSNP","start":140483276,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140483276,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1014912860","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795307824","feature_type":"variation","strand":1,"end":140483279,"alleles":["T","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483279},{"clinical_significance":[],"seq_region_name":"7","id":"rs1185013332","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483280,"feature_type":"variation","strand":1,"end":140483280,"alleles":["C","-"]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483280,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140483280,"clinical_significance":[],"seq_region_name":"7","id":"rs1482333495"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483281,"source":"dbSNP","strand":1,"feature_type":"variation","end":140483281,"alleles":["T","A"],"id":"rs1249004762","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1203129494","source":"dbSNP","start":140483282,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140483282,"alleles":["T","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795307949","feature_type":"variation","strand":1,"end":140483283,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483283},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795307972","feature_type":"variation","strand":1,"end":140483286,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483286},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795308008","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140483291,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483291},{"source":"dbSNP","start":140483297,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140483297,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1321792504"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483300,"feature_type":"variation","strand":1,"end":140483300,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs769752598"},{"feature_type":"variation","strand":1,"end":140483304,"alleles":["G","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483304,"clinical_significance":[],"seq_region_name":"7","id":"rs992187557"},{"feature_type":"variation","strand":1,"end":140483312,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483312,"clinical_significance":[],"seq_region_name":"7","id":"rs550453492"},{"id":"rs1795308128","seq_region_name":"7","clinical_significance":[],"start":140483315,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140483315,"strand":1,"feature_type":"variation"},{"alleles":["T","C"],"end":140483316,"strand":1,"feature_type":"variation","start":140483316,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1795308151","seq_region_name":"7","clinical_significance":[]},{"end":140483319,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140483319,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs948220019","seq_region_name":"7"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483323,"feature_type":"variation","strand":1,"end":140483323,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1029457657"},{"clinical_significance":[],"seq_region_name":"7","id":"rs974298344","end":140483325,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140483325,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795308268","source":"dbSNP","start":140483330,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140483330,"feature_type":"variation","strand":1},{"start":140483331,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","A","G","T"],"end":140483331,"strand":1,"feature_type":"variation","id":"rs562819826","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140483332,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140483332,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs990697208"},{"end":140483333,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140483333,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795308353"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483334,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140483334,"seq_region_name":"7","id":"rs1021781351","clinical_significance":[]},{"id":"rs967650299","seq_region_name":"7","clinical_significance":[],"end":140483337,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140483337,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"end":140483340,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140483340,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1423665599","clinical_significance":[]},{"clinical_significance":[],"id":"rs1471903000","seq_region_name":"7","source":"dbSNP","start":140483341,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140483341,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs749061827","clinical_significance":[],"start":140483344,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","C"],"end":140483344,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140483346,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140483346,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs10227027","seq_region_name":"7"},{"start":140483348,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140483348,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795308629","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483349,"source":"dbSNP","strand":1,"feature_type":"variation","end":140483349,"alleles":["T","TT"],"seq_region_name":"7","id":"rs2130397950","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1488541874","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140483350,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483350},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140483352,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483352,"clinical_significance":[],"id":"rs1371909356","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795308711","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483357,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140483357},{"seq_region_name":"7","id":"rs928289974","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140483358,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483358,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1467702608","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140483364,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483364,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795308769","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483372,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140483372},{"clinical_significance":[],"seq_region_name":"7","id":"rs773990043","alleles":["T","A","C"],"end":140483373,"feature_type":"variation","strand":1,"source":"dbSNP","start":140483373,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"start":140483374,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140483374,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795308844","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795308872","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483379,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140483379},{"seq_region_name":"7","id":"rs1287105130","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483379,"source":"dbSNP","strand":1,"feature_type":"variation","end":140483383,"alleles":["GAGAG","GAG"]},{"feature_type":"variation","strand":1,"end":140483382,"alleles":["A","AA"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483382,"clinical_significance":[],"seq_region_name":"7","id":"rs1795308929"},{"feature_type":"variation","strand":1,"end":140483383,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483383,"clinical_significance":[],"seq_region_name":"7","id":"rs1795308957"},{"alleles":["T","A","C"],"end":140483384,"strand":1,"feature_type":"variation","start":140483384,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs991270363","clinical_significance":[]},{"clinical_significance":[],"id":"rs1230067051","seq_region_name":"7","feature_type":"variation","strand":1,"end":140483386,"alleles":["TCT","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483384},{"seq_region_name":"7","id":"rs1229894456","clinical_significance":[],"start":140483386,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140483386,"alleles":["T","TT"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1219715928","clinical_significance":[],"start":140483387,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140483387,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795309223","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483388,"feature_type":"variation","strand":1,"end":140483392,"alleles":["ACAAC","AC"]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483390,"feature_type":"variation","strand":1,"end":140483390,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs915623992"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483391,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140483391,"clinical_significance":[],"seq_region_name":"7","id":"rs187756752"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483392,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140483392,"id":"rs1320866914","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs931060595","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483393,"source":"dbSNP","strand":1,"feature_type":"variation","end":140483393,"alleles":["G","A","C"]},{"alleles":["T","C"],"end":140483395,"strand":1,"feature_type":"variation","start":140483395,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1363549108","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483401,"feature_type":"variation","strand":1,"end":140483401,"alleles":["C","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1040139709"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1435387624","source":"dbSNP","start":140483402,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140483402,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1048244890","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483403,"source":"dbSNP","strand":1,"feature_type":"variation","end":140483403,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1275661986","source":"dbSNP","start":140483403,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140483409,"alleles":["TGAAGGA","-"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140483404,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483404,"source":"dbSNP","id":"rs1484132290","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140483412,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140483412,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795309562"},{"clinical_significance":[],"id":"rs1453256321","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483412,"feature_type":"variation","strand":1,"alleles":["CAT","-"],"end":140483414},{"clinical_significance":[],"id":"rs1248332392","seq_region_name":"7","source":"dbSNP","start":140483413,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140483413,"feature_type":"variation","strand":1},{"id":"rs1795309632","seq_region_name":"7","clinical_significance":[],"start":140483414,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140483414,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795309657","feature_type":"variation","strand":1,"end":140483421,"alleles":["C","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483421},{"clinical_significance":[],"id":"rs1210174953","seq_region_name":"7","feature_type":"variation","strand":1,"end":140483423,"alleles":["T","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483423},{"source":"dbSNP","start":140483426,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140483426,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1463416530","seq_region_name":"7"},{"start":140483426,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140483430,"alleles":["TGTGT","TGT"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795309721","clinical_significance":[]},{"seq_region_name":"7","id":"rs1203131715","clinical_significance":[],"end":140483430,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140483430,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483438,"source":"dbSNP","strand":1,"feature_type":"variation","end":140483438,"alleles":["G","C"],"seq_region_name":"7","id":"rs886936098","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483439,"source":"dbSNP","strand":1,"feature_type":"variation","end":140483439,"alleles":["G","A"],"seq_region_name":"7","id":"rs1795309782","clinical_significance":[]},{"alleles":["CTGCTAC","C"],"end":140483446,"feature_type":"variation","strand":1,"source":"dbSNP","start":140483440,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1259878518","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1210764764","clinical_significance":[],"strand":1,"feature_type":"variation","end":140483441,"alleles":["T","A","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483441,"source":"dbSNP"},{"alleles":["T","C"],"end":140483444,"feature_type":"variation","strand":1,"source":"dbSNP","start":140483444,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs779622350"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1473452881","source":"dbSNP","start":140483445,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140483445,"alleles":["A","C","G"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140483447,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483447,"source":"dbSNP","seq_region_name":"7","id":"rs1184101132","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130398055","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483450,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140483450},{"seq_region_name":"7","id":"rs1795309984","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483451,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140483451},{"seq_region_name":"7","id":"rs1795310024","clinical_significance":[],"alleles":["T","C"],"end":140483452,"strand":1,"feature_type":"variation","start":140483452,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"start":140483460,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140483460,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130398063","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795310047","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483461,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140483461},{"seq_region_name":"7","id":"rs1412137220","clinical_significance":[],"end":140483463,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140483463,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1040900168","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483464,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140483464},{"seq_region_name":"7","id":"rs775091556","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483468,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140483468},{"clinical_significance":[],"seq_region_name":"7","id":"rs553132930","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483469,"feature_type":"variation","strand":1,"end":140483469,"alleles":["C","A","G","T"]},{"feature_type":"variation","strand":1,"end":140483470,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483470,"clinical_significance":[],"seq_region_name":"7","id":"rs997897386"},{"feature_type":"variation","strand":1,"end":140483471,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483471,"clinical_significance":[],"seq_region_name":"7","id":"rs1433136050"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483473,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140483473,"seq_region_name":"7","id":"rs1359544262","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795310268","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483475,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140483475},{"source":"dbSNP","start":140483477,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140483477,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1303724776"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1468044483","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140483482,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483482},{"clinical_significance":[],"seq_region_name":"7","id":"rs192672436","end":140483485,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140483485,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1205690242","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483486,"feature_type":"variation","strand":1,"end":140483486,"alleles":["G","A"]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483488,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140483488,"clinical_significance":[],"seq_region_name":"7","id":"rs1795310402"},{"strand":1,"feature_type":"variation","end":140483492,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483492,"source":"dbSNP","id":"rs903741359","seq_region_name":"7","clinical_significance":[]},{"start":140483496,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140483496,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795310459","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140483499,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483499,"source":"dbSNP","seq_region_name":"7","id":"rs1585512083","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483507,"source":"dbSNP","strand":1,"feature_type":"variation","end":140483507,"alleles":["A","G"],"seq_region_name":"7","id":"rs1795310498","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs999829885","source":"dbSNP","start":140483509,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140483509,"alleles":["C","T"],"feature_type":"variation","strand":1},{"start":140483511,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140483511,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1169573075","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1031028291","end":140483512,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140483512,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483513,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140483513,"clinical_significance":[],"id":"rs1372044315","seq_region_name":"7"},{"alleles":["A","G"],"end":140483514,"feature_type":"variation","strand":1,"source":"dbSNP","start":140483514,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795310613"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795310631","alleles":["C","G"],"end":140483516,"feature_type":"variation","strand":1,"source":"dbSNP","start":140483516,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"alleles":["C","T"],"end":140483524,"strand":1,"feature_type":"variation","start":140483524,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs184417449","clinical_significance":[]},{"source":"dbSNP","start":140483528,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140483528,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1013661195"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140483529,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483529,"source":"dbSNP","seq_region_name":"7","id":"rs1023635891","clinical_significance":[]},{"source":"dbSNP","start":140483530,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140483530,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1484103146"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483535,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140483535,"seq_region_name":"7","id":"rs1795310736","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1327607829","feature_type":"variation","strand":1,"end":140483540,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483540},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483541,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140483541,"seq_region_name":"7","id":"rs1795310801","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483543,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140483543,"seq_region_name":"7","id":"rs1795310814","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483544,"source":"dbSNP","strand":1,"feature_type":"variation","end":140483544,"alleles":["T","C"],"id":"rs1795310837","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1254244370","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140483545,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483545},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483546,"feature_type":"variation","strand":1,"end":140483546,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795310864"},{"end":140483548,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140483548,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs551681373"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795310904","source":"dbSNP","start":140483549,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140483549,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs969536509","clinical_significance":[],"alleles":["T","C"],"end":140483552,"strand":1,"feature_type":"variation","start":140483552,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"id":"rs1738454050","seq_region_name":"7","clinical_significance":[],"start":140483554,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140483554,"strand":1,"feature_type":"variation"},{"id":"rs1343020301","seq_region_name":"7","clinical_significance":[],"end":140483557,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140483557,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"id":"rs1450185969","seq_region_name":"7","alleles":["A","T"],"end":140483558,"feature_type":"variation","strand":1,"source":"dbSNP","start":140483558,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"start":140483560,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140483560,"strand":1,"feature_type":"variation","id":"rs1795310971","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483561,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140483561,"clinical_significance":[],"seq_region_name":"7","id":"rs1226473941"},{"seq_region_name":"7","id":"rs974182129","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140483562,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483562,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1313693471","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483565,"source":"dbSNP","strand":1,"feature_type":"variation","end":140483568,"alleles":["CCCC","CCCCC"]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483569,"source":"dbSNP","strand":1,"feature_type":"variation","end":140483569,"alleles":["A","G"],"seq_region_name":"7","id":"rs1795311105","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483576,"feature_type":"variation","strand":1,"end":140483576,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1398228754"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1377392638","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483583,"feature_type":"variation","strand":1,"end":140483583,"alleles":["C","A"]},{"id":"rs1585512126","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140483585,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483585,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795311154","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483586,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140483586},{"alleles":["A","G"],"end":140483587,"feature_type":"variation","strand":1,"source":"dbSNP","start":140483587,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795311164","seq_region_name":"7"},{"start":140483588,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140483588,"alleles":["G","C"],"strand":1,"feature_type":"variation","id":"rs1795311184","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","A"],"end":140483591,"strand":1,"feature_type":"variation","start":140483591,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1312859258","clinical_significance":[]},{"seq_region_name":"7","id":"rs889220970","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140483595,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483595,"source":"dbSNP"},{"alleles":["T","C"],"end":140483597,"strand":1,"feature_type":"variation","start":140483597,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1795311226","clinical_significance":[]},{"start":140483598,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140483598,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795311247","clinical_significance":[]},{"alleles":["A","G"],"end":140483599,"feature_type":"variation","strand":1,"source":"dbSNP","start":140483599,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1370671243"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795311288","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483603,"feature_type":"variation","strand":1,"end":140483603,"alleles":["T","C"]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483604,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140483604,"seq_region_name":"7","id":"rs545537692","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140483606,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483606,"clinical_significance":[],"seq_region_name":"7","id":"rs1795311331"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1021835296","alleles":["C","G","T"],"end":140483612,"feature_type":"variation","strand":1,"source":"dbSNP","start":140483612,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs189290542","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","C","T"],"end":140483613,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483613,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140483615,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483615,"source":"dbSNP","id":"rs1165030373","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795311494","source":"dbSNP","start":140483616,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140483616,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140483618,"alleles":["G","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483618,"clinical_significance":[],"id":"rs764667229","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1795311541","seq_region_name":"7","alleles":["G","A"],"end":140483619,"feature_type":"variation","strand":1,"source":"dbSNP","start":140483619,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483620,"source":"dbSNP","strand":1,"feature_type":"variation","end":140483620,"alleles":["G","A"],"id":"rs1795311568","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795311607","source":"dbSNP","start":140483621,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140483621,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1425373063","clinical_significance":[],"end":140483623,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140483623,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs1795311653","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483624,"source":"dbSNP","strand":1,"feature_type":"variation","end":140483624,"alleles":["G","A"]},{"end":140483628,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140483628,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs2130398249","clinical_significance":[]},{"clinical_significance":[],"id":"rs1255104961","seq_region_name":"7","end":140483629,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140483629,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1187157737","end":140483634,"alleles":["C","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140483634,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795311713","clinical_significance":[],"end":140483635,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140483635,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"strand":1,"feature_type":"variation","end":140483636,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483636,"source":"dbSNP","seq_region_name":"7","id":"rs1795311731","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795311751","source":"dbSNP","start":140483641,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140483641,"alleles":["G","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs977679028","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140483644,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483644},{"end":140483645,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140483645,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1483306462","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795311808","seq_region_name":"7","source":"dbSNP","start":140483650,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140483650,"feature_type":"variation","strand":1},{"start":140483654,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140483654,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1254090961","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483656,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140483656,"clinical_significance":[],"seq_region_name":"7","id":"rs1035917557"},{"alleles":["T","C"],"end":140483657,"feature_type":"variation","strand":1,"source":"dbSNP","start":140483657,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs2130398275","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483663,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140483663,"seq_region_name":"7","id":"rs959754484","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795311879","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140483667,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483667},{"id":"rs1795311910","seq_region_name":"7","clinical_significance":[],"end":140483670,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140483670,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"start":140483672,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140483672,"strand":1,"feature_type":"variation","id":"rs1795311931","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140483675,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483675,"source":"dbSNP","seq_region_name":"7","id":"rs1299477176","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1266304890","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483685,"feature_type":"variation","strand":1,"end":140483685,"alleles":["T","C"]},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140483689,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483689,"clinical_significance":[],"seq_region_name":"7","id":"rs991586654"},{"clinical_significance":[],"id":"rs1795311992","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483691,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140483691},{"clinical_significance":[],"id":"rs777963975","seq_region_name":"7","source":"dbSNP","start":140483700,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["TTTGTTTGTTT","TTTGTTT"],"end":140483710,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140483700,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["TTTGTTTGTTTCTTTGTTTGTTT","TTTGTTTGTTT"],"end":140483722,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795312044"},{"clinical_significance":[],"id":"rs1272457909","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483703,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140483703},{"seq_region_name":"7","id":"rs1443047590","clinical_significance":[],"end":140483706,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140483706,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795312297","source":"dbSNP","start":140483707,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140483707,"alleles":["G","C"],"feature_type":"variation","strand":1},{"end":140483708,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140483708,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs983427414","clinical_significance":[]},{"source":"dbSNP","start":140483708,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140483714,"alleles":["TTTCTTT","TTT"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795312334","seq_region_name":"7"},{"source":"dbSNP","start":140483711,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140483711,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1352804631"},{"seq_region_name":"7","id":"rs1389243479","clinical_significance":[],"end":140483722,"alleles":["TTTGTTTGTTT","TTTGTTT"],"strand":1,"feature_type":"variation","start":140483712,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"feature_type":"variation","strand":1,"alleles":["TTTGTTTGTTTTGTTTGTTTTG","TTTGTTTGTTTTG"],"end":140483733,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483712,"clinical_significance":[],"seq_region_name":"7","id":"rs1795312406"},{"alleles":["G","-"],"end":140483715,"strand":1,"feature_type":"variation","start":140483715,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1795312426","clinical_significance":[]},{"alleles":["TTT","TTTT"],"end":140483718,"strand":1,"feature_type":"variation","start":140483716,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1212912878","clinical_significance":[]},{"seq_region_name":"7","id":"rs907568514","clinical_significance":[],"start":140483721,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["TTTGTTTGTTT","TTTGTTT"],"end":140483731,"strand":1,"feature_type":"variation"},{"end":140483728,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140483728,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs530958362"},{"start":140483731,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140483731,"strand":1,"feature_type":"variation","id":"rs944352730","seq_region_name":"7","clinical_significance":[]},{"end":140483733,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140483733,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1453920999"},{"feature_type":"variation","strand":1,"end":140483738,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483738,"clinical_significance":[],"seq_region_name":"7","id":"rs1795312552"},{"clinical_significance":[],"id":"rs543329030","seq_region_name":"7","alleles":["G","C"],"end":140483740,"feature_type":"variation","strand":1,"source":"dbSNP","start":140483740,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140483745,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140483745,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs9648842","seq_region_name":"7"},{"alleles":["G","A"],"end":140483746,"strand":1,"feature_type":"variation","start":140483746,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs114396382","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1189627103","end":140483749,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140483749,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483751,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140483751,"seq_region_name":"7","id":"rs757688870","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795312728","seq_region_name":"7","source":"dbSNP","start":140483752,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140483752,"alleles":["T","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130398376","source":"dbSNP","start":140483757,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140483757,"alleles":["T","C"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140483769,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483769,"source":"dbSNP","seq_region_name":"7","id":"rs1414182675","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795312767","seq_region_name":"7","end":140483771,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140483771,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483772,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140483772,"clinical_significance":[],"seq_region_name":"7","id":"rs1795312787"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140483774,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483774,"clinical_significance":[],"seq_region_name":"7","id":"rs1795312806"},{"alleles":["G","A"],"end":140483776,"strand":1,"feature_type":"variation","start":140483776,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1795312822","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140483777,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483777,"clinical_significance":[],"seq_region_name":"7","id":"rs1795312841"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483778,"feature_type":"variation","strand":1,"end":140483778,"alleles":["A","G"],"clinical_significance":[],"id":"rs1179534752","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140483782,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483782,"clinical_significance":[],"seq_region_name":"7","id":"rs1795312884"},{"start":140483783,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140483783,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs983833730","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795312908","feature_type":"variation","strand":1,"end":140483788,"alleles":["C","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483788},{"end":140483791,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140483791,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1437369661"},{"alleles":["G","A"],"end":140483792,"feature_type":"variation","strand":1,"source":"dbSNP","start":140483792,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs931817437","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483793,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140483793,"seq_region_name":"7","id":"rs1795312948","clinical_significance":[]},{"seq_region_name":"7","id":"rs1043544921","clinical_significance":[],"start":140483796,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140483796,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"alleles":["CCCC","CCC"],"end":140483800,"feature_type":"variation","strand":1,"source":"dbSNP","start":140483797,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795313026"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1392342539","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483798,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140483798},{"seq_region_name":"7","id":"rs1758119784","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483799,"source":"dbSNP","strand":1,"feature_type":"variation","end":140483799,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563102607","feature_type":"variation","strand":1,"end":140483801,"alleles":["A","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483801},{"seq_region_name":"7","id":"rs1795313095","clinical_significance":[],"alleles":["C","T"],"end":140483802,"strand":1,"feature_type":"variation","start":140483802,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795313110","source":"dbSNP","start":140483803,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140483803,"alleles":["C","T"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140483807,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483807,"clinical_significance":[],"seq_region_name":"7","id":"rs9648843"},{"clinical_significance":[],"id":"rs144891594","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483808,"feature_type":"variation","strand":1,"end":140483808,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1040952674","source":"dbSNP","start":140483810,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140483810,"feature_type":"variation","strand":1},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483811,"feature_type":"variation","strand":1,"end":140483811,"alleles":["C","A"],"clinical_significance":[],"id":"rs1229457362","seq_region_name":"7"},{"id":"rs1795313563","seq_region_name":"7","clinical_significance":[],"start":140483814,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140483814,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1795313582","clinical_significance":[],"end":140483815,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140483815,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"id":"rs149040646","seq_region_name":"7","end":140483817,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140483817,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs896488642","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483818,"feature_type":"variation","strand":1,"end":140483818,"alleles":["G","A","T"]},{"clinical_significance":[],"id":"rs1795313724","seq_region_name":"7","alleles":["A","G"],"end":140483819,"feature_type":"variation","strand":1,"source":"dbSNP","start":140483819,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"end":140483824,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140483824,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1013505891","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140483825,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483825,"clinical_significance":[],"id":"rs1023686744","seq_region_name":"7"},{"source":"dbSNP","start":140483832,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140483832,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1672981992"},{"feature_type":"variation","strand":1,"end":140483836,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483836,"clinical_significance":[],"seq_region_name":"7","id":"rs969420808"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1388169576","feature_type":"variation","strand":1,"end":140483847,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483847},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483850,"feature_type":"variation","strand":1,"end":140483850,"alleles":["G","T"],"clinical_significance":[],"id":"rs1795314127","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795314151","feature_type":"variation","strand":1,"end":140483852,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483852},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795314184","end":140483854,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140483854,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795314216","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140483855,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483855,"source":"dbSNP"},{"alleles":["A","C"],"end":140483860,"feature_type":"variation","strand":1,"source":"dbSNP","start":140483860,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs932563917"},{"seq_region_name":"7","id":"rs1324802289","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483865,"source":"dbSNP","strand":1,"feature_type":"variation","end":140483865,"alleles":["C","A"]},{"seq_region_name":"7","id":"rs1391911185","clinical_significance":[],"start":140483865,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["CCC","CC"],"end":140483867,"strand":1,"feature_type":"variation"},{"id":"rs1795314689","seq_region_name":"7","clinical_significance":[],"start":140483870,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140483870,"alleles":["A","-"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1050884467","feature_type":"variation","strand":1,"end":140483871,"alleles":["C","A","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483871},{"clinical_significance":[],"seq_region_name":"7","id":"rs143072221","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483872,"feature_type":"variation","strand":1,"end":140483872,"alleles":["G","A","C"]},{"start":140483873,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140483873,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795314814","clinical_significance":[]},{"source":"dbSNP","start":140483884,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140483884,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1469529602"},{"clinical_significance":[],"id":"rs1795314870","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","TT"],"end":140483888,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483888},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483890,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140483890,"clinical_significance":[],"seq_region_name":"7","id":"rs1795314880"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795314892","end":140483893,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140483893,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140483896,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140483896,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1027185032"},{"strand":1,"feature_type":"variation","end":140483903,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483903,"source":"dbSNP","id":"rs62490453","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483905,"source":"dbSNP","strand":1,"feature_type":"variation","end":140483905,"alleles":["G","C","T"],"id":"rs1043129797","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs903366614","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483906,"source":"dbSNP","strand":1,"feature_type":"variation","end":140483906,"alleles":["G","A"]},{"start":140483911,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140483911,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs983095227","clinical_significance":[]},{"end":140483912,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140483912,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1209557770"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483914,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140483914,"clinical_significance":[],"id":"rs1585512276","seq_region_name":"7"},{"seq_region_name":"7","id":"rs2130398539","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140483916,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483916,"source":"dbSNP"},{"id":"rs1466566708","seq_region_name":"7","clinical_significance":[],"end":140483929,"alleles":["TGATGTCCTAGCTG","TG"],"strand":1,"feature_type":"variation","start":140483916,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"seq_region_name":"7","id":"rs999002958","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483917,"source":"dbSNP","strand":1,"feature_type":"variation","end":140483917,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1205089285","feature_type":"variation","strand":1,"end":140483918,"alleles":["A","G","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483918},{"id":"rs569293075","seq_region_name":"7","clinical_significance":[],"end":140483919,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140483919,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs975719089","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140483920,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483920},{"seq_region_name":"7","id":"rs1585512294","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483921,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140483921},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140483922,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483922,"clinical_significance":[],"id":"rs1795315168","seq_region_name":"7"},{"end":140483926,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140483926,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs960597767","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs746968380","feature_type":"variation","strand":1,"end":140483934,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483934},{"seq_region_name":"7","id":"rs538453933","clinical_significance":[],"end":140483935,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140483935,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"start":140483940,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140483940,"strand":1,"feature_type":"variation","id":"rs1023093140","seq_region_name":"7","clinical_significance":[]},{"start":140483943,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["GGG","GG"],"end":140483945,"strand":1,"feature_type":"variation","id":"rs1795315259","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","A"],"end":140483945,"feature_type":"variation","strand":1,"source":"dbSNP","start":140483945,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795315269"},{"start":140483946,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140483946,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795315298","clinical_significance":[]},{"seq_region_name":"7","id":"rs1269799502","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140483947,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483947,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1435305503","feature_type":"variation","strand":1,"end":140483951,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483951},{"start":140483954,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140483954,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1367134934","clinical_significance":[]},{"source":"dbSNP","start":140483957,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140483957,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs979581206"},{"id":"rs925177854","seq_region_name":"7","clinical_significance":[],"start":140483958,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140483967,"alleles":["TCTTGTCTTG","TCTTG"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1402896598","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483960,"feature_type":"variation","strand":1,"end":140483960,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1795315427","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483967,"source":"dbSNP","strand":1,"feature_type":"variation","end":140483967,"alleles":["G","A"]},{"start":140483968,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140483968,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs952343123","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795315467","end":140483974,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140483974,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140483975,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140483975,"clinical_significance":[],"seq_region_name":"7","id":"rs983841821"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483983,"source":"dbSNP","strand":1,"feature_type":"variation","end":140483983,"alleles":["A","G"],"id":"rs1221039560","seq_region_name":"7","clinical_significance":[]},{"id":"rs1795315529","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140483986,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483986,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs536687811","source":"dbSNP","start":140483990,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140483990,"alleles":["C","T"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140483993,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140483993,"source":"dbSNP","seq_region_name":"7","id":"rs1394531908","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1189478188","alleles":["C","T"],"end":140483996,"feature_type":"variation","strand":1,"source":"dbSNP","start":140483996,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795315621","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484000,"source":"dbSNP","strand":1,"feature_type":"variation","end":140484000,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1795315635","clinical_significance":[],"strand":1,"feature_type":"variation","end":140484006,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484006,"source":"dbSNP"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484010,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140484010,"clinical_significance":[],"seq_region_name":"7","id":"rs1585512334"},{"strand":1,"feature_type":"variation","alleles":["C","A","G"],"end":140484012,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484012,"source":"dbSNP","id":"rs1795315677","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs908270099","clinical_significance":[],"strand":1,"feature_type":"variation","end":140484015,"alleles":["T","A","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484015,"source":"dbSNP"},{"source":"dbSNP","start":140484022,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140484022,"alleles":["A","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1192997632"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1443352479","end":140484022,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140484022,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"alleles":["G","A"],"end":140484024,"strand":1,"feature_type":"variation","start":140484024,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1795315794","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130398635","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140484027,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484027,"source":"dbSNP"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484028,"feature_type":"variation","strand":1,"end":140484028,"alleles":["C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs138705485"},{"clinical_significance":[],"seq_region_name":"7","id":"rs567399165","end":140484033,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140484033,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"id":"rs922445839","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140484034,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484034,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140484035,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484035,"clinical_significance":[],"id":"rs2130398647","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795315913","source":"dbSNP","start":140484037,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140484037,"alleles":["C","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1585512352","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140484039,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484039,"source":"dbSNP"},{"start":140484040,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140484040,"alleles":["G","C"],"strand":1,"feature_type":"variation","id":"rs1193415361","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","G"],"end":140484042,"feature_type":"variation","strand":1,"source":"dbSNP","start":140484042,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795315963"},{"alleles":["T","C"],"end":140484043,"strand":1,"feature_type":"variation","start":140484043,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1795315988","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1345148611","clinical_significance":[],"strand":1,"feature_type":"variation","end":140484051,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484051,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1585512359","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140484052,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484052,"source":"dbSNP"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484054,"feature_type":"variation","strand":1,"end":140484054,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795316045"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1045067918","source":"dbSNP","start":140484056,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140484056,"alleles":["A","G"],"feature_type":"variation","strand":1},{"start":140484060,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140484060,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs932593109","clinical_significance":[]},{"clinical_significance":[],"id":"rs558244004","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140484062,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484062},{"clinical_significance":[],"seq_region_name":"7","id":"rs1250356613","feature_type":"variation","strand":1,"end":140484064,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484064},{"clinical_significance":[],"id":"rs142764436","seq_region_name":"7","end":140484066,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140484066,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1192872765","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484070,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140484070},{"id":"rs1795316174","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140484071,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484071,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795316194","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140484072,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484072,"source":"dbSNP"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484078,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140484078,"clinical_significance":[],"seq_region_name":"7","id":"rs4726825"},{"seq_region_name":"7","id":"rs1340811272","clinical_significance":[],"start":140484080,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140484080,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"end":140484082,"alleles":["A","C","G","T"],"strand":1,"feature_type":"variation","start":140484082,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs192761377","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795316359","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484084,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140484084},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130398727","alleles":["A","T"],"end":140484088,"feature_type":"variation","strand":1,"source":"dbSNP","start":140484088,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"end":140484091,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140484091,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585512389"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1043183349","feature_type":"variation","strand":1,"end":140484094,"alleles":["C","G","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484094},{"seq_region_name":"7","id":"rs1795316408","clinical_significance":[],"start":140484097,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140484097,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140484099,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140484099,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1169223722","seq_region_name":"7"},{"id":"rs540679834","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484101,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140484101},{"start":140484104,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140484104,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1417725488","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140484107,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484107,"source":"dbSNP","seq_region_name":"7","id":"rs796365349","clinical_significance":[]},{"id":"rs1795316497","seq_region_name":"7","clinical_significance":[],"start":140484108,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140484108,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"alleles":["G","A"],"end":140484111,"feature_type":"variation","strand":1,"source":"dbSNP","start":140484111,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1473360340"},{"seq_region_name":"7","id":"rs1795316530","clinical_significance":[],"end":140484115,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140484115,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585512405","source":"dbSNP","start":140484116,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140484116,"alleles":["A","C"],"feature_type":"variation","strand":1},{"end":140484120,"alleles":["T","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140484120,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1019878925"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1427979808","source":"dbSNP","start":140484121,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140484121,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484129,"source":"dbSNP","strand":1,"feature_type":"variation","end":140484129,"alleles":["A","C"],"id":"rs1457755045","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130398778","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140484135,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484135,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1485593262","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484137,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140484137},{"clinical_significance":[],"seq_region_name":"7","id":"rs1161251557","feature_type":"variation","strand":1,"end":140484155,"alleles":["TAACAACATGTTGTATTAA","TAA"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484137},{"end":140484140,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140484140,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795316681","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484143,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140484143,"id":"rs1563102679","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1256212741","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140484145,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484145},{"clinical_significance":[],"seq_region_name":"7","id":"rs965598326","alleles":["T","C"],"end":140484147,"feature_type":"variation","strand":1,"source":"dbSNP","start":140484147,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484151,"feature_type":"variation","strand":1,"end":140484151,"alleles":["A","G"],"clinical_significance":[],"id":"rs1795316755","seq_region_name":"7"},{"end":140484159,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140484159,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1795316786","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1308745708","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484163,"source":"dbSNP","strand":1,"feature_type":"variation","end":140484163,"alleles":["C","-"]},{"source":"dbSNP","start":140484164,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140484164,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795316835","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1270494835","clinical_significance":[],"end":140484168,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140484168,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484171,"feature_type":"variation","strand":1,"end":140484171,"alleles":["A","C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs545499040"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484178,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140484178,"clinical_significance":[],"id":"rs538974550","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484180,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140484180,"seq_region_name":"7","id":"rs1795316947","clinical_significance":[]},{"id":"rs575702036","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140484183,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484183,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140484184,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484184,"clinical_significance":[],"seq_region_name":"7","id":"rs1331917805"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484190,"source":"dbSNP","strand":1,"feature_type":"variation","end":140484190,"alleles":["G","A"],"seq_region_name":"7","id":"rs768910054","clinical_significance":[]},{"seq_region_name":"7","id":"rs1231380618","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["GGGG","GGG"],"end":140484193,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484190,"source":"dbSNP"},{"source":"dbSNP","start":140484192,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140484192,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1013589544","seq_region_name":"7"},{"id":"rs1795317095","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484201,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140484201},{"clinical_significance":[],"id":"rs1308561712","seq_region_name":"7","source":"dbSNP","start":140484206,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140484206,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs747428641","feature_type":"variation","strand":1,"alleles":["-","T"],"end":140484206,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484207},{"source":"dbSNP","start":140484208,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140484208,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795317156","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795317182","clinical_significance":[],"end":140484212,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140484212,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"id":"rs1795317205","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484213,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140484213},{"start":140484218,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140484218,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs542702030","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1352819014","source":"dbSNP","start":140484219,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140484219,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484222,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140484222,"id":"rs184614121","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140484223,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140484223,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795317320"},{"clinical_significance":[],"id":"rs1795317350","seq_region_name":"7","alleles":["T","C"],"end":140484225,"feature_type":"variation","strand":1,"source":"dbSNP","start":140484225,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140484226,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140484226,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795317368"},{"id":"rs1795317397","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140484227,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484227,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1328465060","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140484229,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484229},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795317445","end":140484231,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140484231,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795317469","clinical_significance":[],"end":140484233,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140484233,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484240,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140484240,"id":"rs1406130557","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585512472","clinical_significance":[],"strand":1,"feature_type":"variation","end":140484242,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484242,"source":"dbSNP"},{"source":"dbSNP","start":140484250,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140484250,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795317522"},{"end":140484254,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140484254,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1795317548","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484255,"feature_type":"variation","strand":1,"end":140484255,"alleles":["C","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795317563"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484258,"feature_type":"variation","strand":1,"end":140484258,"alleles":["A","G"],"clinical_significance":[],"id":"rs1795317597","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1281530415","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484260,"source":"dbSNP","strand":1,"feature_type":"variation","end":140484260,"alleles":["T","C"]},{"source":"dbSNP","start":140484261,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140484261,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795317654"},{"strand":1,"feature_type":"variation","alleles":["A","C","T"],"end":140484269,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484269,"source":"dbSNP","seq_region_name":"7","id":"rs188716833","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795317719","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484273,"source":"dbSNP","strand":1,"feature_type":"variation","end":140484273,"alleles":["C","T"]},{"clinical_significance":[],"id":"rs1163156450","seq_region_name":"7","alleles":["G","C"],"end":140484277,"feature_type":"variation","strand":1,"source":"dbSNP","start":140484277,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795317751","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["GG","G"],"end":140484282,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484281,"source":"dbSNP"},{"end":140484282,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140484282,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1475078512","clinical_significance":[]},{"alleles":["TTTTT","TTTT","TTTTTT"],"end":140484290,"strand":1,"feature_type":"variation","start":140484286,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1184930493","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1229601768","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484290,"feature_type":"variation","strand":1,"end":140484290,"alleles":["T","G"]},{"clinical_significance":[],"id":"rs979206103","seq_region_name":"7","feature_type":"variation","strand":1,"end":140484291,"alleles":["G","A","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484291},{"clinical_significance":[],"seq_region_name":"7","id":"rs781408681","feature_type":"variation","strand":1,"end":140484299,"alleles":["TATT","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484296},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795317948","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140484297,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484297},{"strand":1,"feature_type":"variation","end":140484298,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484298,"source":"dbSNP","seq_region_name":"7","id":"rs1795317963","clinical_significance":[]},{"end":140484299,"alleles":["TT","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140484298,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs924989920"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484298,"feature_type":"variation","strand":1,"end":140484307,"alleles":["TTGTTGTTGT","TTGTTGT"],"clinical_significance":[],"seq_region_name":"7","id":"rs935191480"},{"id":"rs1795318067","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140484300,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484300,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795318090","source":"dbSNP","start":140484302,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140484302,"alleles":["T","G"],"feature_type":"variation","strand":1},{"end":140484303,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140484303,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1389452086"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484304,"source":"dbSNP","strand":1,"feature_type":"variation","end":140484304,"alleles":["T","C"],"id":"rs555789861","seq_region_name":"7","clinical_significance":[]},{"start":140484308,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140484308,"alleles":["G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1333847743","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484310,"feature_type":"variation","strand":1,"end":140484310,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1288971102"},{"clinical_significance":[],"id":"rs1225349801","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484311,"feature_type":"variation","strand":1,"end":140484311,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1795318244","clinical_significance":[],"start":140484312,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A"],"end":140484312,"strand":1,"feature_type":"variation"},{"id":"rs1795318270","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140484314,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484314,"source":"dbSNP"},{"source":"dbSNP","start":140484320,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140484320,"alleles":["G","C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1371317946"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484322,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140484322,"seq_region_name":"7","id":"rs1563102711","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484324,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140484324,"clinical_significance":[],"id":"rs1005152132","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140484325,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484325,"source":"dbSNP","seq_region_name":"7","id":"rs1795318361","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795318395","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484327,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140484327},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484329,"feature_type":"variation","strand":1,"end":140484329,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795318423"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484329,"source":"dbSNP","strand":1,"feature_type":"variation","end":140484368,"alleles":["ATGGAATCTCGCTCTGTCGCCCAGACTGGGGTGCAGGTGC","-"],"seq_region_name":"7","id":"rs1795318447","clinical_significance":[]},{"seq_region_name":"7","id":"rs1278966043","clinical_significance":[],"alleles":["T","-"],"end":140484337,"strand":1,"feature_type":"variation","start":140484337,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"start":140484338,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140484338,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1015195633","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140484339,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484339,"clinical_significance":[],"seq_region_name":"7","id":"rs1349102158"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140484342,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484342,"source":"dbSNP","seq_region_name":"7","id":"rs1397033018","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs988356053","source":"dbSNP","start":140484345,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140484345,"alleles":["T","C"],"feature_type":"variation","strand":1},{"alleles":["C","T"],"end":140484346,"feature_type":"variation","strand":1,"source":"dbSNP","start":140484346,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs917731337"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484347,"feature_type":"variation","strand":1,"end":140484347,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795318605"},{"alleles":["C","G"],"end":140484349,"feature_type":"variation","strand":1,"source":"dbSNP","start":140484349,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1389813074"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140484351,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484351,"clinical_significance":[],"seq_region_name":"7","id":"rs949332957"},{"source":"dbSNP","start":140484353,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140484353,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1417806664"},{"seq_region_name":"7","id":"rs1405165314","clinical_significance":[],"start":140484355,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140484355,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"alleles":["TG","-"],"end":140484356,"feature_type":"variation","strand":1,"source":"dbSNP","start":140484355,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795318981"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484356,"feature_type":"variation","strand":1,"end":140484356,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795319002"},{"seq_region_name":"7","id":"rs1176066422","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140484359,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484359,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs961138146","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484360,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140484360},{"id":"rs879195592","seq_region_name":"7","clinical_significance":[],"end":140484361,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140484361,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484365,"source":"dbSNP","strand":1,"feature_type":"variation","end":140484365,"alleles":["G","A","T"],"id":"rs1795319078","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140484368,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140484368,"alleles":["C","A","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs181447372"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140484369,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484369,"source":"dbSNP","seq_region_name":"7","id":"rs186252026","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795319207","clinical_significance":[],"alleles":["T","C"],"end":140484371,"strand":1,"feature_type":"variation","start":140484371,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs189402353","alleles":["C","T"],"end":140484374,"feature_type":"variation","strand":1,"source":"dbSNP","start":140484374,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"start":140484375,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","A","T"],"end":140484375,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs985795292","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484379,"source":"dbSNP","strand":1,"feature_type":"variation","end":140484379,"alleles":["C","T"],"seq_region_name":"7","id":"rs1314997162","clinical_significance":[]},{"alleles":["C","T"],"end":140484381,"feature_type":"variation","strand":1,"source":"dbSNP","start":140484381,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795319344"},{"clinical_significance":[],"id":"rs1196286737","seq_region_name":"7","feature_type":"variation","strand":1,"end":140484386,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484386},{"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140484388,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484388,"clinical_significance":[],"seq_region_name":"7","id":"rs1267611654"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795319395","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484388,"feature_type":"variation","strand":1,"alleles":["C","-"],"end":140484388},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484394,"source":"dbSNP","strand":1,"feature_type":"variation","end":140484394,"alleles":["C","T"],"seq_region_name":"7","id":"rs1795319408","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795319435","clinical_significance":[],"strand":1,"feature_type":"variation","end":140484396,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484396,"source":"dbSNP"},{"source":"dbSNP","start":140484397,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140484397,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795319453","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1585512565","clinical_significance":[],"start":140484398,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","TT"],"end":140484398,"strand":1,"feature_type":"variation"},{"end":140484406,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140484406,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1585512568","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795319543","source":"dbSNP","start":140484407,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140484407,"alleles":["G","C"],"feature_type":"variation","strand":1},{"start":140484408,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","A","C"],"end":140484408,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs11974767","clinical_significance":[]},{"source":"dbSNP","start":140484409,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140484409,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795319607"},{"alleles":["C","T"],"end":140484413,"strand":1,"feature_type":"variation","start":140484413,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1795319644","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130399077","feature_type":"variation","strand":1,"end":140484415,"alleles":["T","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484415},{"source":"dbSNP","start":140484418,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140484418,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795319660"},{"clinical_significance":[],"id":"rs1283460076","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484424,"feature_type":"variation","strand":1,"end":140484424,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1795319680","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484426,"source":"dbSNP","strand":1,"feature_type":"variation","end":140484426,"alleles":["C","G"]},{"seq_region_name":"7","id":"rs774213627","clinical_significance":[],"alleles":["C","T"],"end":140484428,"strand":1,"feature_type":"variation","start":140484428,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"start":140484430,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140484430,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs554038788","clinical_significance":[]},{"seq_region_name":"7","id":"rs532601813","clinical_significance":[],"start":140484431,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140484431,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs931268397","source":"dbSNP","start":140484432,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140484432,"alleles":["A","G"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140484433,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140484433,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1409697233","seq_region_name":"7"},{"start":140484434,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140484434,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795319866","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795319888","source":"dbSNP","start":140484436,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["GCTGGGACTACAGGCGC","GC"],"end":140484452,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140484439,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140484439,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1048482985"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140484441,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484441,"source":"dbSNP","seq_region_name":"7","id":"rs1795319934","clinical_significance":[]},{"seq_region_name":"7","id":"rs1163629441","clinical_significance":[],"start":140484443,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140484443,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1392612218","feature_type":"variation","strand":1,"end":140484445,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484445},{"start":140484446,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140484446,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795320029","clinical_significance":[]},{"end":140484447,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140484447,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795320054"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140484448,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484448,"clinical_significance":[],"seq_region_name":"7","id":"rs1795320074"},{"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140484450,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484450,"clinical_significance":[],"seq_region_name":"7","id":"rs745466085"},{"start":140484451,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140484451,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs1177389056","seq_region_name":"7","clinical_significance":[]},{"id":"rs574312824","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484457,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140484457},{"seq_region_name":"7","id":"rs771791296","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484458,"source":"dbSNP","strand":1,"feature_type":"variation","end":140484458,"alleles":["A","C","G"]},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140484459,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484459,"clinical_significance":[],"seq_region_name":"7","id":"rs1795320255"},{"alleles":["CC","C"],"end":140484460,"strand":1,"feature_type":"variation","start":140484459,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs2130399135","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795320281","seq_region_name":"7","feature_type":"variation","strand":1,"end":140484460,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484460},{"seq_region_name":"7","id":"rs1004406139","clinical_significance":[],"alleles":["A","G"],"end":140484461,"strand":1,"feature_type":"variation","start":140484461,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484462,"feature_type":"variation","strand":1,"end":140484462,"alleles":["T","C"],"clinical_significance":[],"id":"rs1191398672","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795320378","alleles":["C","A"],"end":140484464,"feature_type":"variation","strand":1,"source":"dbSNP","start":140484464,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140484466,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484466,"source":"dbSNP","id":"rs1585512611","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484468,"source":"dbSNP","strand":1,"feature_type":"variation","end":140484468,"alleles":["G","A"],"seq_region_name":"7","id":"rs1795320413","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484470,"source":"dbSNP","strand":1,"feature_type":"variation","end":140484470,"alleles":["T","A"],"seq_region_name":"7","id":"rs1795320439","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484473,"feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140484473,"clinical_significance":[],"seq_region_name":"7","id":"rs1795320468"},{"clinical_significance":[],"seq_region_name":"7","id":"rs924599601","alleles":["T","C"],"end":140484484,"feature_type":"variation","strand":1,"source":"dbSNP","start":140484484,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1585512615","seq_region_name":"7","end":140484487,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140484487,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1301500795","source":"dbSNP","start":140484490,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140484490,"feature_type":"variation","strand":1},{"alleles":["G","A","T"],"end":140484492,"feature_type":"variation","strand":1,"source":"dbSNP","start":140484492,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1453352360"},{"source":"dbSNP","start":140484495,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140484495,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1410539815"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1365147740","source":"dbSNP","start":140484495,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["GGGG","GGGGG"],"end":140484498,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484496,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140484496,"seq_region_name":"7","id":"rs1188112563","clinical_significance":[]},{"alleles":["G","A"],"end":140484497,"strand":1,"feature_type":"variation","start":140484497,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1343076815","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795320920","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484498,"source":"dbSNP","strand":1,"feature_type":"variation","end":140484498,"alleles":["G","T"]},{"seq_region_name":"7","id":"rs1241484917","clinical_significance":[],"strand":1,"feature_type":"variation","end":140484499,"alleles":["T","A","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484499,"source":"dbSNP"},{"seq_region_name":"7","id":"rs934772376","clinical_significance":[],"strand":1,"feature_type":"variation","end":140484504,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484504,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1057179503","feature_type":"variation","strand":1,"end":140484507,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484507},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484508,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140484508,"clinical_significance":[],"seq_region_name":"7","id":"rs1238951394"},{"source":"dbSNP","start":140484512,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140484512,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585512638"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1233847714","alleles":["G","T"],"end":140484517,"feature_type":"variation","strand":1,"source":"dbSNP","start":140484517,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1795321055","seq_region_name":"7","feature_type":"variation","strand":1,"end":140484520,"alleles":["G","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484520},{"id":"rs1343061900","seq_region_name":"7","clinical_significance":[],"start":140484521,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","T"],"end":140484521,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484522,"source":"dbSNP","strand":1,"feature_type":"variation","end":140484522,"alleles":["T","G"],"id":"rs1795321085","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140484525,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484525,"clinical_significance":[],"seq_region_name":"7","id":"rs895981952"},{"end":140484526,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140484526,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1358878231","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484527,"feature_type":"variation","strand":1,"end":140484528,"alleles":["AA","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1361675063"},{"seq_region_name":"7","id":"rs1795321140","clinical_significance":[],"alleles":["A","C"],"end":140484528,"strand":1,"feature_type":"variation","start":140484528,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs182003243","source":"dbSNP","start":140484529,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140484529,"alleles":["C","A","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795321220","source":"dbSNP","start":140484530,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140484530,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140484534,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484534,"clinical_significance":[],"id":"rs1795321239","seq_region_name":"7"},{"source":"dbSNP","start":140484535,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140484535,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1045059864"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484536,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140484536,"clinical_significance":[],"seq_region_name":"7","id":"rs1483152792"},{"id":"rs1795321315","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484537,"source":"dbSNP","strand":1,"feature_type":"variation","end":140484537,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1206702194","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140484539,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484539,"source":"dbSNP"},{"start":140484542,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","C"],"end":140484542,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1028538926","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140484548,"alleles":["TGATTG","TGATTGATTG"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484543,"source":"dbSNP","seq_region_name":"7","id":"rs1795321412","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484544,"source":"dbSNP","strand":1,"feature_type":"variation","end":140484544,"alleles":["G","A"],"seq_region_name":"7","id":"rs953031224","clinical_significance":[]},{"seq_region_name":"7","id":"rs979477839","clinical_significance":[],"start":140484546,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140484546,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1188149981","alleles":["G","A"],"end":140484549,"feature_type":"variation","strand":1,"source":"dbSNP","start":140484549,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484554,"feature_type":"variation","strand":1,"end":140484554,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs888722174"},{"clinical_significance":[],"id":"rs1795321551","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484555,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140484555},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795321577","feature_type":"variation","strand":1,"end":140484557,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484557},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140484564,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484564,"source":"dbSNP","id":"rs1172050563","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1370027090","end":140484566,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140484566,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1005745975","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140484567,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484567},{"end":140484569,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140484569,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795321686"},{"strand":1,"feature_type":"variation","end":140484570,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484570,"source":"dbSNP","seq_region_name":"7","id":"rs1426567823","clinical_significance":[]},{"start":140484572,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140484572,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795321741","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1260715800","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484573,"feature_type":"variation","strand":1,"end":140484590,"alleles":["TGGGATTACAGGCATGGG","TGGG"]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484575,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140484575,"clinical_significance":[],"id":"rs1795321791","seq_region_name":"7"},{"source":"dbSNP","start":140484579,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140484579,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1182408586"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1015244882","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140484580,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484580},{"seq_region_name":"7","id":"rs1486572899","clinical_significance":[],"end":140484581,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140484581,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484583,"feature_type":"variation","strand":1,"end":140484583,"alleles":["G","A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1255503659"},{"feature_type":"variation","strand":1,"alleles":["CATGGGCCCTGCCCATG","CATG"],"end":140484601,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484585,"clinical_significance":[],"seq_region_name":"7","id":"rs1795321911"},{"clinical_significance":[],"id":"rs2130399286","seq_region_name":"7","source":"dbSNP","start":140484586,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140484586,"feature_type":"variation","strand":1},{"alleles":["T","C"],"end":140484587,"feature_type":"variation","strand":1,"source":"dbSNP","start":140484587,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795321943"},{"source":"dbSNP","start":140484589,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140484589,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795321963","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484590,"source":"dbSNP","strand":1,"feature_type":"variation","end":140484590,"alleles":["G","A"],"id":"rs896821366","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs998344287","clinical_significance":[],"start":140484594,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140484594,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484595,"feature_type":"variation","strand":1,"end":140484595,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs530520802"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795322065","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140484596,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484596},{"end":140484597,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140484597,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1032109198","seq_region_name":"7","clinical_significance":[]},{"start":140484599,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","C","G"],"end":140484599,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1029378546","clinical_significance":[]},{"source":"dbSNP","start":140484600,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140484600,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1253354505"},{"clinical_significance":[],"id":"rs1795322171","seq_region_name":"7","source":"dbSNP","start":140484602,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140484602,"alleles":["T","C"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140484606,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140484606,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795322198"},{"alleles":["TGT","T"],"end":140484612,"strand":1,"feature_type":"variation","start":140484610,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs987894670","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140484611,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484611,"source":"dbSNP","id":"rs1307321610","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs572543163","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484612,"feature_type":"variation","strand":1,"end":140484618,"alleles":["TTTTTTT","TTTTTT","TTTTTTTT"]},{"seq_region_name":"7","id":"rs548658256","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484616,"source":"dbSNP","strand":1,"feature_type":"variation","end":140484616,"alleles":["T","A"]},{"alleles":["T","C"],"end":140484617,"feature_type":"variation","strand":1,"source":"dbSNP","start":140484617,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795322298"},{"id":"rs954033471","seq_region_name":"7","clinical_significance":[],"start":140484618,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","A"],"end":140484618,"strand":1,"feature_type":"variation"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484619,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140484619,"clinical_significance":[],"seq_region_name":"7","id":"rs567272206"},{"feature_type":"variation","strand":1,"end":140484620,"alleles":["A","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484620,"clinical_significance":[],"seq_region_name":"7","id":"rs1310005499"},{"seq_region_name":"7","id":"rs1394404647","clinical_significance":[],"alleles":["T","C"],"end":140484621,"strand":1,"feature_type":"variation","start":140484621,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"strand":1,"feature_type":"variation","end":140484624,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484624,"source":"dbSNP","seq_region_name":"7","id":"rs1022126000","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1413679336","end":140484629,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140484629,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"end":140484630,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140484630,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs868691233","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795322454","alleles":["G","C"],"end":140484631,"feature_type":"variation","strand":1,"source":"dbSNP","start":140484631,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs978000818","clinical_significance":[],"start":140484633,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140484633,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140484635,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140484635,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs931345099"},{"feature_type":"variation","strand":1,"end":140484637,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484637,"clinical_significance":[],"seq_region_name":"7","id":"rs1372292800"},{"source":"dbSNP","start":140484640,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140484640,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795322526"},{"strand":1,"feature_type":"variation","end":140484641,"alleles":["T","C","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484641,"source":"dbSNP","id":"rs1165300903","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140484642,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484642,"clinical_significance":[],"seq_region_name":"7","id":"rs1795322573"},{"alleles":["CCCC","CCCCCC"],"end":140484647,"strand":1,"feature_type":"variation","start":140484644,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1476055248","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140484645,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484645,"clinical_significance":[],"id":"rs75529260","seq_region_name":"7"},{"alleles":["C","T"],"end":140484646,"feature_type":"variation","strand":1,"source":"dbSNP","start":140484646,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs908524672"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585512720","feature_type":"variation","strand":1,"end":140484647,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484647},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795322661","source":"dbSNP","start":140484655,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140484655,"alleles":["C","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1244271009","clinical_significance":[],"start":140484656,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140484656,"alleles":["C","A","G","T"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140484660,"alleles":["G","A","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484660,"clinical_significance":[],"id":"rs940131856","seq_region_name":"7"},{"seq_region_name":"7","id":"rs546903682","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484661,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140484661},{"clinical_significance":[],"seq_region_name":"7","id":"rs761977954","source":"dbSNP","start":140484664,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140484664,"alleles":["T","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795322786","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484668,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140484668},{"start":140484672,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","A"],"end":140484672,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs996981766","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs917315590","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484673,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140484673},{"alleles":["G","A","C"],"end":140484675,"feature_type":"variation","strand":1,"source":"dbSNP","start":140484675,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795322848"},{"seq_region_name":"7","id":"rs1333113346","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484676,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140484676},{"start":140484677,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140484677,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1293267834","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795322894","clinical_significance":[],"start":140484683,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140484683,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140484684,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140484684,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795322914","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130399431","feature_type":"variation","strand":1,"end":140484687,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484687},{"feature_type":"variation","strand":1,"end":140484692,"alleles":["CC","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484691,"clinical_significance":[],"id":"rs1795322932","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140484703,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484703,"clinical_significance":[],"seq_region_name":"7","id":"rs1795322960"},{"feature_type":"variation","strand":1,"end":140484704,"alleles":["T","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484704,"clinical_significance":[],"seq_region_name":"7","id":"rs1050016520"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795323010","source":"dbSNP","start":140484707,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140484707,"alleles":["C","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs948796322","source":"dbSNP","start":140484708,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140484708,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140484710,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484710,"source":"dbSNP","seq_region_name":"7","id":"rs904748556","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140484711,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484711,"clinical_significance":[],"seq_region_name":"7","id":"rs2130399446"},{"clinical_significance":[],"id":"rs75932365","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484714,"feature_type":"variation","strand":1,"end":140484714,"alleles":["A","C","G","T"]},{"clinical_significance":[],"id":"rs1201006078","seq_region_name":"7","end":140484717,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140484717,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795323167","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484724,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140484724},{"seq_region_name":"7","id":"rs1795323192","clinical_significance":[],"end":140484725,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140484725,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"alleles":["G","A"],"end":140484726,"feature_type":"variation","strand":1,"source":"dbSNP","start":140484726,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795323209"},{"id":"rs1795323231","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140484727,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484727,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795323254","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484729,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140484729},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795323276","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484731,"feature_type":"variation","strand":1,"end":140484731,"alleles":["C","T"]},{"alleles":["G","A"],"end":140484735,"strand":1,"feature_type":"variation","start":140484735,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1258208967","clinical_significance":[]},{"start":140484741,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140484741,"alleles":["G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1032451788","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795323356","clinical_significance":[],"start":140484744,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","C"],"end":140484744,"strand":1,"feature_type":"variation"},{"alleles":["G","A"],"end":140484748,"feature_type":"variation","strand":1,"source":"dbSNP","start":140484748,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs888604812"},{"id":"rs1248402865","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484749,"source":"dbSNP","strand":1,"feature_type":"variation","end":140484749,"alleles":["T","A"]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484752,"feature_type":"variation","strand":1,"end":140484752,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1009311682"},{"seq_region_name":"7","id":"rs1024642423","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140484753,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484753,"source":"dbSNP"},{"start":140484754,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140484754,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130399508","clinical_significance":[]},{"seq_region_name":"7","id":"rs1179820815","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484760,"source":"dbSNP","strand":1,"feature_type":"variation","end":140484760,"alleles":["T","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795323538","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484766,"feature_type":"variation","strand":1,"end":140484766,"alleles":["G","T"]},{"seq_region_name":"7","id":"rs941654061","clinical_significance":[],"strand":1,"feature_type":"variation","end":140484767,"alleles":["A","C","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484767,"source":"dbSNP"},{"alleles":["C","T"],"end":140484769,"strand":1,"feature_type":"variation","start":140484769,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1795323593","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795323620","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484776,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140484776},{"end":140484777,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140484777,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795323645","seq_region_name":"7"},{"source":"dbSNP","start":140484778,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140484778,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs980546025"},{"seq_region_name":"7","id":"rs1195712220","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140484787,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484787,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140484798,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484798,"source":"dbSNP","id":"rs1795323957","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1467431644","clinical_significance":[],"strand":1,"feature_type":"variation","end":140484800,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484800,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795323996","clinical_significance":[],"start":140484803,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","T"],"end":140484803,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1795324015","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484805,"source":"dbSNP","strand":1,"feature_type":"variation","end":140484805,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1795324028","clinical_significance":[],"end":140484807,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140484807,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"id":"rs1795324050","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484811,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","-"],"end":140484811},{"seq_region_name":"7","id":"rs1209910709","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484812,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140484812},{"source":"dbSNP","start":140484812,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140484817,"alleles":["GGGGGG","GGGGG","GGGGGGG"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1272899169"},{"seq_region_name":"7","id":"rs1037204395","clinical_significance":[],"start":140484813,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140484813,"alleles":["G","A","C","T"],"strand":1,"feature_type":"variation"},{"id":"rs1795324145","seq_region_name":"7","clinical_significance":[],"start":140484814,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","C"],"end":140484814,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563102800","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484815,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140484815},{"strand":1,"feature_type":"variation","alleles":["GGGTGC","GGGTGCGGGTGC"],"end":140484820,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484815,"source":"dbSNP","id":"rs539801309","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130399573","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484815,"source":"dbSNP","strand":1,"feature_type":"variation","end":140484820,"alleles":["GGGTGC","-"]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484816,"feature_type":"variation","strand":1,"alleles":["G","C","T"],"end":140484816,"clinical_significance":[],"seq_region_name":"7","id":"rs896832740"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484817,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140484817,"id":"rs538878237","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484819,"feature_type":"variation","strand":1,"end":140484819,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1442601783"},{"strand":1,"feature_type":"variation","end":140484820,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484820,"source":"dbSNP","id":"rs1368524889","seq_region_name":"7","clinical_significance":[]},{"end":140484823,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140484823,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1795324260","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1324910979","clinical_significance":[],"start":140484824,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140484824,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"end":140484826,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140484826,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs563110215"},{"end":140484836,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140484836,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795324310"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1029725854","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484839,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140484839},{"id":"rs889574636","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484840,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140484840},{"seq_region_name":"7","id":"rs768345626","clinical_significance":[],"strand":1,"feature_type":"variation","end":140484849,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484849,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1387133627","source":"dbSNP","start":140484850,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140484850,"alleles":["C","A"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484851,"source":"dbSNP","strand":1,"feature_type":"variation","end":140484856,"alleles":["AGAAGA","AGA"],"id":"rs1156713010","seq_region_name":"7","clinical_significance":[]},{"end":140484856,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140484856,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs374459869"},{"clinical_significance":[],"id":"rs1795324498","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484857,"feature_type":"variation","strand":1,"end":140484857,"alleles":["T","A"]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484858,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140484858,"clinical_significance":[],"seq_region_name":"7","id":"rs1022176626"},{"clinical_significance":[],"seq_region_name":"7","id":"rs967835047","feature_type":"variation","strand":1,"end":140484861,"alleles":["T","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484861},{"start":140484862,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140484862,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795324549","clinical_significance":[]},{"seq_region_name":"7","id":"rs939994722","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484864,"source":"dbSNP","strand":1,"feature_type":"variation","end":140484864,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795324592","source":"dbSNP","start":140484869,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140484869,"alleles":["C","T"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484875,"source":"dbSNP","strand":1,"feature_type":"variation","end":140484875,"alleles":["C","A","G"],"seq_region_name":"7","id":"rs1585512819","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484876,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140484876,"clinical_significance":[],"seq_region_name":"7","id":"rs62490454"},{"source":"dbSNP","start":140484880,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140484880,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795324702"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1451014457","source":"dbSNP","start":140484883,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140484883,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140484883,"alleles":["T","TT"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484883,"source":"dbSNP","id":"rs1795324743","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1336566280","clinical_significance":[],"start":140484885,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["G","C"],"end":140484885,"strand":1,"feature_type":"variation"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484887,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140484887,"clinical_significance":[],"seq_region_name":"7","id":"rs1252777669"},{"start":140484888,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","A","C"],"end":140484888,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs773384132","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795324828","clinical_significance":[],"strand":1,"feature_type":"variation","end":140484892,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484892,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484893,"source":"dbSNP","strand":1,"feature_type":"variation","end":140484893,"alleles":["G","A"],"seq_region_name":"7","id":"rs1030895302","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795324852","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484896,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140484896},{"alleles":["G","A"],"end":140484897,"feature_type":"variation","strand":1,"source":"dbSNP","start":140484897,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795324871","seq_region_name":"7"},{"seq_region_name":"7","id":"rs2130399691","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484912,"source":"dbSNP","strand":1,"feature_type":"variation","end":140484912,"alleles":["A","G"]},{"alleles":["C","A"],"end":140484918,"feature_type":"variation","strand":1,"source":"dbSNP","start":140484918,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs765647746"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130399705","feature_type":"variation","strand":1,"end":140484922,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484922},{"feature_type":"variation","strand":1,"end":140484940,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484940,"clinical_significance":[],"seq_region_name":"7","id":"rs750829768"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140484942,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484942,"source":"dbSNP","seq_region_name":"7","id":"rs932823546","clinical_significance":[]},{"source":"dbSNP","start":140484943,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140484943,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1205034921"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1352381604","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484945,"feature_type":"variation","strand":1,"end":140484945,"alleles":["A","C"]},{"clinical_significance":[],"id":"rs1280337348","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484946,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140484946},{"seq_region_name":"7","id":"rs1236064074","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484954,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140484954},{"start":140484956,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140484956,"alleles":["G","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs575762480","clinical_significance":[]},{"end":140484959,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140484959,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1049944630","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484960,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140484960,"clinical_significance":[],"seq_region_name":"7","id":"rs2130399729"},{"clinical_significance":[],"id":"rs904676203","seq_region_name":"7","feature_type":"variation","strand":1,"end":140484963,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484963},{"source":"dbSNP","start":140484964,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140484964,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130399738"},{"clinical_significance":[],"seq_region_name":"7","id":"rs992866189","end":140484966,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140484966,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"start":140484968,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140484968,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1327959152","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140484971,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484971,"clinical_significance":[],"seq_region_name":"7","id":"rs1795326447"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140484972,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140484972,"clinical_significance":[],"id":"rs910699401","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795326515","clinical_significance":[],"end":140484974,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140484974,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484976,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140484976,"id":"rs1795326547","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1381536382","clinical_significance":[],"end":140484983,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140484983,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"strand":1,"feature_type":"variation","end":140484986,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484986,"source":"dbSNP","seq_region_name":"7","id":"rs536766139","clinical_significance":[]},{"alleles":["A","T"],"end":140484988,"strand":1,"feature_type":"variation","start":140484988,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1314763645","clinical_significance":[]},{"clinical_significance":[],"id":"rs1306519599","seq_region_name":"7","source":"dbSNP","start":140484990,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140484990,"feature_type":"variation","strand":1},{"id":"rs1585512875","seq_region_name":"7","clinical_significance":[],"start":140484993,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140484993,"alleles":["G","A","C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs79283273","clinical_significance":[],"strand":1,"feature_type":"variation","end":140484997,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140484997,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795326731","end":140484998,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140484998,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140485002,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140485002,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs763266726"},{"clinical_significance":[],"id":"rs1476619954","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140485005,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485005},{"seq_region_name":"7","id":"rs1683554545","clinical_significance":[],"start":140485006,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140485006,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1795326929","seq_region_name":"7","feature_type":"variation","strand":1,"end":140485007,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485007},{"seq_region_name":"7","id":"rs941497297","clinical_significance":[],"start":140485008,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140485008,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"start":140485010,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140485010,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1371647540","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140485011,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485011,"clinical_significance":[],"seq_region_name":"7","id":"rs2130399794"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1037258204","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485012,"feature_type":"variation","strand":1,"end":140485012,"alleles":["A","T"]},{"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140485016,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485016,"clinical_significance":[],"id":"rs187506431","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1486254039","seq_region_name":"7","feature_type":"variation","strand":1,"end":140485020,"alleles":["G","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485020},{"id":"rs1260218034","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140485021,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140485021,"source":"dbSNP"},{"start":140485028,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140485028,"strand":1,"feature_type":"variation","id":"rs540553812","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485030,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140485030,"clinical_significance":[],"id":"rs190639456","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1484386998","clinical_significance":[],"start":140485034,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140485034,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140485037,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140485037,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795327415"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485039,"feature_type":"variation","strand":1,"alleles":["G","C","T"],"end":140485039,"clinical_significance":[],"seq_region_name":"7","id":"rs1795327448"},{"clinical_significance":[],"seq_region_name":"7","id":"rs59738001","feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140485042,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485042},{"source":"dbSNP","start":140485046,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140485046,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795327610"},{"seq_region_name":"7","id":"rs544350251","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140485047,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140485047,"source":"dbSNP"},{"source":"dbSNP","start":140485048,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140485048,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795327650"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140485049,"source":"dbSNP","strand":1,"feature_type":"variation","end":140485049,"alleles":["C","A"],"seq_region_name":"7","id":"rs1292226636","clinical_significance":[]},{"seq_region_name":"7","id":"rs1341250346","clinical_significance":[],"end":140485050,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140485050,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"start":140485051,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140485051,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1050817797","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1217949877","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485052,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140485052},{"seq_region_name":"7","id":"rs766783563","clinical_significance":[],"start":140485052,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140485053,"alleles":["CT","-"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140485052,"source":"dbSNP","strand":1,"feature_type":"variation","end":140485057,"alleles":["CTGTCT","CT"],"seq_region_name":"7","id":"rs1248462410","clinical_significance":[]},{"source":"dbSNP","start":140485053,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140485053,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795327846"},{"source":"dbSNP","start":140485054,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140485054,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1356075152"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140485058,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485058,"clinical_significance":[],"id":"rs1314641681","seq_region_name":"7"},{"start":140485059,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140485067,"alleles":["TTATCTTAT","TTAT"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1413052299","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1024694157","end":140485061,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140485061,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140485067,"alleles":["T","C"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485067,"clinical_significance":[],"seq_region_name":"7","id":"rs1329814741"},{"seq_region_name":"7","id":"rs544281900","clinical_significance":[],"start":140485071,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","A"],"end":140485071,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140485078,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140485078,"source":"dbSNP","seq_region_name":"7","id":"rs1795328035","clinical_significance":[]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485078,"feature_type":"variation","strand":1,"alleles":["AGGAAGGAAG","AGGAAG"],"end":140485087,"clinical_significance":[],"seq_region_name":"7","id":"rs772087695"},{"feature_type":"variation","strand":1,"end":140485080,"alleles":["G","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485080,"clinical_significance":[],"id":"rs1795328120","seq_region_name":"7"},{"source":"dbSNP","start":140485083,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140485083,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795328145"},{"seq_region_name":"7","id":"rs562571849","clinical_significance":[],"strand":1,"feature_type":"variation","end":140485084,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140485084,"source":"dbSNP"},{"start":140485090,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140485090,"alleles":["C","A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs562750453","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140485095,"source":"dbSNP","strand":1,"feature_type":"variation","end":140485095,"alleles":["A","G"],"seq_region_name":"7","id":"rs1006646030","clinical_significance":[]},{"start":140485096,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["T","A"],"end":140485096,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1033962198","clinical_significance":[]},{"end":140485097,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140485097,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795328430"},{"seq_region_name":"7","id":"rs367921904","clinical_significance":[],"start":140485104,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140485104,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140485112,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485112,"clinical_significance":[],"id":"rs984445740","seq_region_name":"7"},{"start":140485116,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140485116,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795328554","clinical_significance":[]},{"seq_region_name":"7","id":"rs1186400181","clinical_significance":[],"end":140485118,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140485118,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"end":140485121,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140485121,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795328596","seq_region_name":"7"},{"start":140485124,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140485124,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs549086416","clinical_significance":[]},{"source":"dbSNP","start":140485126,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140485126,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795328655"},{"id":"rs560701403","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140485128,"source":"dbSNP","strand":1,"feature_type":"variation","end":140485128,"alleles":["A","T"]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140485131,"source":"dbSNP","strand":1,"feature_type":"variation","end":140485131,"alleles":["A","G"],"seq_region_name":"7","id":"rs999334762","clinical_significance":[]},{"end":140485133,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140485133,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795328711"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140485135,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140485135,"source":"dbSNP","seq_region_name":"7","id":"rs1030820248","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795328743","clinical_significance":[],"start":140485137,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140485137,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140485145,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485145,"clinical_significance":[],"seq_region_name":"7","id":"rs1795328758"},{"seq_region_name":"7","id":"rs528125977","clinical_significance":[],"strand":1,"feature_type":"variation","end":140485150,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140485150,"source":"dbSNP"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485154,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140485154,"clinical_significance":[],"seq_region_name":"7","id":"rs6966907"},{"alleles":["T","C"],"end":140485156,"strand":1,"feature_type":"variation","start":140485156,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1270428108","clinical_significance":[]},{"start":140485159,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","T"],"end":140485159,"strand":1,"feature_type":"variation","id":"rs1176309243","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130399935","feature_type":"variation","strand":1,"end":140485162,"alleles":["A","G"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485162},{"end":140485164,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140485164,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795328909"},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140485169,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485169,"clinical_significance":[],"seq_region_name":"7","id":"rs1389895452"},{"source":"dbSNP","start":140485170,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140485170,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs922578213"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140485178,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140485178,"seq_region_name":"7","id":"rs1795328965","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140485192,"source":"dbSNP","strand":1,"feature_type":"variation","end":140485192,"alleles":["C","G"],"seq_region_name":"7","id":"rs1795328986","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130399950","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140485194,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140485194},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795329005","source":"dbSNP","start":140485199,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140485199,"alleles":["C","G"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140485200,"source":"dbSNP","strand":1,"feature_type":"variation","end":140485200,"alleles":["C","T"],"seq_region_name":"7","id":"rs1024348743","clinical_significance":[]},{"seq_region_name":"7","id":"rs970424041","clinical_significance":[],"start":140485201,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140485201,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140485202,"source":"dbSNP","strand":1,"feature_type":"variation","end":140485202,"alleles":["T","C"],"seq_region_name":"7","id":"rs980163636","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs909940293","feature_type":"variation","strand":1,"end":140485209,"alleles":["T","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485209},{"clinical_significance":[],"seq_region_name":"7","id":"rs1053788901","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485210,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140485210},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485211,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140485211,"clinical_significance":[],"id":"rs571616875","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795329285","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140485215,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485215},{"feature_type":"variation","strand":1,"end":140485220,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485220,"clinical_significance":[],"seq_region_name":"7","id":"rs182880821"},{"source":"dbSNP","start":140485225,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140485225,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs550756041"},{"strand":1,"feature_type":"variation","end":140485229,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140485229,"source":"dbSNP","seq_region_name":"7","id":"rs1795329339","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140485232,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485232,"clinical_significance":[],"seq_region_name":"7","id":"rs2130399988"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485236,"feature_type":"variation","strand":1,"end":140485236,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795329351"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140485241,"source":"dbSNP","strand":1,"feature_type":"variation","end":140485241,"alleles":["A","G"],"id":"rs186154211","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["ACTACT","ACT","ACTACTACT"],"end":140485246,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485241,"clinical_significance":[],"seq_region_name":"7","id":"rs1328402804"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140485244,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140485244,"source":"dbSNP","id":"rs1795329424","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795329443","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485245,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140485245},{"source":"dbSNP","start":140485247,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140485247,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795329465","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795329481","source":"dbSNP","start":140485248,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140485248,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140485250,"alleles":["T","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485250,"clinical_significance":[],"seq_region_name":"7","id":"rs1795329495"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140485261,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140485261,"id":"rs1343067463","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140485268,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140485268,"source":"dbSNP","id":"rs1397080102","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs200783399","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140485275,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485275},{"source":"dbSNP","start":140485277,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140485277,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795329569"},{"seq_region_name":"7","id":"rs1268723469","clinical_significance":[],"alleles":["A","C"],"end":140485278,"strand":1,"feature_type":"variation","start":140485278,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"source":"dbSNP","start":140485280,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140485280,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1331066380"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130400046","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485284,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140485284},{"clinical_significance":[],"id":"rs1795329625","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140485285,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485285},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140485288,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140485288,"source":"dbSNP","seq_region_name":"7","id":"rs1051748017","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795329662","clinical_significance":[],"end":140485289,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140485289,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485290,"feature_type":"variation","strand":1,"end":140485290,"alleles":["C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795329677"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1213405799","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485292,"feature_type":"variation","strand":1,"end":140485292,"alleles":["A","C","T"]},{"source":"dbSNP","start":140485294,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140485294,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795329698"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140485297,"source":"dbSNP","strand":1,"feature_type":"variation","end":140485297,"alleles":["G","A","T"],"seq_region_name":"7","id":"rs1177597072","clinical_significance":[]},{"alleles":["C","A","T"],"end":140485299,"strand":1,"feature_type":"variation","start":140485299,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1468766039","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140485301,"source":"dbSNP","strand":1,"feature_type":"variation","end":140485301,"alleles":["C","T"],"id":"rs910899747","seq_region_name":"7","clinical_significance":[]},{"start":140485302,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140485302,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs942316142","clinical_significance":[]},{"source":"dbSNP","start":140485305,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140485305,"alleles":["T","A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1001945478"},{"strand":1,"feature_type":"variation","end":140485309,"alleles":["GGA","-"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140485307,"source":"dbSNP","seq_region_name":"7","id":"rs1211744799","clinical_significance":[]},{"source":"dbSNP","start":140485309,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140485309,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795329804","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563102911","alleles":["T","C"],"end":140485312,"feature_type":"variation","strand":1,"source":"dbSNP","start":140485312,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1043515572","end":140485313,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140485313,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"start":140485314,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140485314,"alleles":["G","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795329880","clinical_significance":[]},{"end":140485315,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140485315,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs2130400091","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1765766125","alleles":["T","C"],"end":140485317,"feature_type":"variation","strand":1,"source":"dbSNP","start":140485317,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"end":140485323,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140485323,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs888282790"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795329920","alleles":["C","-"],"end":140485323,"feature_type":"variation","strand":1,"source":"dbSNP","start":140485323,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140485324,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140485328,"alleles":["TGTGT","TGT"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795329934","seq_region_name":"7"},{"end":140485327,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140485327,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795329947","seq_region_name":"7"},{"start":140485329,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["C","G"],"end":140485329,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130400104","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795329964","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140485330,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140485330},{"end":140485333,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140485333,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs370761479"},{"source":"dbSNP","start":140485334,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140485334,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs999261101"},{"clinical_significance":[],"seq_region_name":"7","id":"rs138122892","feature_type":"variation","strand":1,"end":140485336,"alleles":["C","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485336},{"clinical_significance":[],"id":"rs1373656497","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485340,"feature_type":"variation","strand":1,"end":140485340,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1186367411","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140485340,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CCC","CCCC"],"end":140485342},{"clinical_significance":[],"id":"rs1795330120","seq_region_name":"7","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485341,"feature_type":"variation","strand":1,"end":140485341,"alleles":["C","A"]},{"start":140485345,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140485345,"strand":1,"feature_type":"variation","id":"rs1436185897","seq_region_name":"7","clinical_significance":[]},{"start":140485346,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140485349,"alleles":["CCCC","CCCCC"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1271203927","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140485348,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140485348,"source":"dbSNP","seq_region_name":"7","id":"rs1795330255","clinical_significance":[]},{"seq_region_name":"7","id":"rs896303686","clinical_significance":[],"end":140485349,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140485349,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"strand":1,"feature_type":"variation","end":140485350,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140485350,"source":"dbSNP","seq_region_name":"7","id":"rs1368427973","clinical_significance":[]},{"source":"dbSNP","start":140485353,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","end":140485353,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795331592"},{"strand":1,"feature_type":"variation","end":140485356,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140485356,"source":"dbSNP","seq_region_name":"7","id":"rs1479480887","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs753717082","alleles":["T","C"],"end":140485365,"feature_type":"variation","strand":1,"source":"dbSNP","start":140485365,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795331688","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140485368,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485368},{"clinical_significance":[],"seq_region_name":"7","id":"rs538440085","end":140485370,"alleles":["G","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140485370,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795331712","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485370,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140485370},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485372,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140485372,"clinical_significance":[],"seq_region_name":"7","id":"rs1198737185"},{"clinical_significance":[],"seq_region_name":"7","id":"rs141781271","end":140485373,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140485373,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140485385,"source":"dbSNP","strand":1,"feature_type":"variation","end":140485385,"alleles":["T","G"],"seq_region_name":"7","id":"rs1795331830","clinical_significance":[]},{"alleles":["C","T"],"end":140485389,"strand":1,"feature_type":"variation","start":140485389,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1795331862","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795331885","seq_region_name":"7","end":140485391,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140485391,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"alleles":["C","A","T"],"end":140485392,"strand":1,"feature_type":"variation","start":140485392,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1454392864","clinical_significance":[]},{"id":"rs1254480184","seq_region_name":"7","clinical_significance":[],"start":140485394,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140485396,"alleles":["TTT","TT"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1795331968","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["-","TAATCAGTTTTCTCTATTA"],"end":140485396,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485397},{"seq_region_name":"7","id":"rs1795331991","clinical_significance":[],"end":140485397,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140485397,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"start":140485400,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","C"],"end":140485400,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1191587606","clinical_significance":[]},{"id":"rs1795332035","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140485403,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"TF_binding_site_variant","start":140485403,"source":"dbSNP"},{"alleles":["A","G"],"end":140485405,"feature_type":"variation","strand":1,"source":"dbSNP","start":140485405,"consequence_type":"TF_binding_site_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585513075"},{"id":"rs1421328798","seq_region_name":"7","clinical_significance":[],"alleles":["TTTTT","TTTT"],"end":140485410,"strand":1,"feature_type":"variation","start":140485406,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"TF_binding_site_variant"},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140485414,"consequence_type":"TF_binding_site_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485414,"clinical_significance":[],"id":"rs1488017936","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs150600473","end":140485417,"alleles":["G","A","C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140485417,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"start":140485421,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140485421,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795332158","clinical_significance":[]},{"alleles":["T","G"],"end":140485424,"feature_type":"variation","strand":1,"source":"dbSNP","start":140485424,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1217805882"},{"alleles":["G","T"],"end":140485429,"strand":1,"feature_type":"variation","start":140485429,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs954024201","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140485430,"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140485430,"source":"dbSNP","seq_region_name":"7","id":"rs985951716","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795332232","source":"dbSNP","start":140485431,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140485431,"feature_type":"variation","strand":1},{"id":"rs1235320453","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140485434,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AGGAGGA","AGGA"],"end":140485440},{"alleles":["G","A"],"end":140485435,"feature_type":"variation","strand":1,"source":"dbSNP","start":140485435,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795332276","seq_region_name":"7"},{"source":"dbSNP","start":140485436,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140485436,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795332291","seq_region_name":"7"},{"seq_region_name":"7","id":"rs970096018","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140485437,"source":"dbSNP","strand":1,"feature_type":"variation","end":140485437,"alleles":["A","C","G"]},{"start":140485438,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["GG","G"],"end":140485439,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795332336","clinical_significance":[]},{"alleles":["G","A"],"end":140485439,"feature_type":"variation","strand":1,"source":"dbSNP","start":140485439,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1301516788"},{"seq_region_name":"7","id":"rs745647800","clinical_significance":[],"end":140485442,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140485442,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"feature_type":"variation","strand":1,"end":140485445,"alleles":["C","A","G","T"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485445,"clinical_significance":[],"id":"rs1363061681","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140485446,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","-"],"end":140485446,"seq_region_name":"7","id":"rs1291167358","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140485446,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140485446,"source":"dbSNP","id":"rs1429190078","seq_region_name":"7","clinical_significance":[]},{"start":140485449,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","end":140485449,"alleles":["G","T"],"strand":1,"feature_type":"variation","id":"rs534244078","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1358078095","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485450,"feature_type":"variation","strand":1,"end":140485450,"alleles":["C","T"]},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485451,"feature_type":"variation","strand":1,"end":140485451,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs558530160"},{"end":140485452,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140485452,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","id":"rs1434796880","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1585513105","seq_region_name":"7","end":140485453,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140485453,"consequence_type":"intergenic_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs77779168","clinical_significance":[],"strand":1,"feature_type":"variation","end":140485454,"alleles":["G","C","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140485454,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1795332621","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140485455,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485455},{"seq_region_name":"7","id":"rs1795332642","clinical_significance":[],"strand":1,"feature_type":"variation","end":140485459,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140485459,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1585513112","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140485460,"source":"dbSNP","strand":1,"feature_type":"variation","end":140485460,"alleles":["T","G"]},{"start":140485461,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","alleles":["A","G"],"end":140485461,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs913373630","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140485465,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140485465,"source":"dbSNP","seq_region_name":"7","id":"rs779749938","clinical_significance":[]},{"id":"rs1419921278","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140485467,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140485467},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795332901","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485469,"feature_type":"variation","strand":1,"end":140485469,"alleles":["C","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1188213404","feature_type":"variation","strand":1,"end":140485474,"alleles":["C","A"],"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485474},{"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140485478,"source":"dbSNP","strand":1,"feature_type":"variation","end":140485478,"alleles":["G","A"],"id":"rs1795332941","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140485485,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485485,"clinical_significance":[],"seq_region_name":"7","id":"rs1484821086"},{"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485489,"feature_type":"variation","strand":1,"end":140485489,"alleles":["T","C"],"clinical_significance":[],"id":"rs1795333001","seq_region_name":"7"},{"source":"dbSNP","start":140485492,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140485492,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1585513122","seq_region_name":"7"},{"seq_region_name":"7","id":"rs962802948","clinical_significance":[],"end":140485495,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140485495,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"feature_type":"variation","strand":1,"alleles":["TTTT","TTTTTT"],"end":140485498,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485495,"clinical_significance":[],"seq_region_name":"7","id":"rs1795333080"},{"seq_region_name":"7","id":"rs1262369198","clinical_significance":[],"end":140485498,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140485498,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563102940","consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485499,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140485499},{"clinical_significance":[],"seq_region_name":"7","id":"rs747159502","feature_type":"variation","strand":1,"alleles":["AGAG","AG"],"end":140485503,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485500},{"alleles":["G","A"],"end":140485501,"strand":1,"feature_type":"variation","start":140485501,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intergenic_variant","seq_region_name":"7","id":"rs1795333190","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795333214","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intergenic_variant","start":140485504,"source":"dbSNP","strand":1,"feature_type":"variation","end":140485504,"alleles":["T","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs190302419","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140485505,"consequence_type":"intergenic_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485505},{"clinical_significance":[],"id":"rs1278514712","seq_region_name":"7","end":140485513,"alleles":["TC","TCTC"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140485512,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38"},{"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485515,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140485515,"clinical_significance":[],"seq_region_name":"7","id":"rs1795333294"},{"seq_region_name":"7","id":"rs972789805","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140485520,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140485520},{"clinical_significance":[],"seq_region_name":"7","id":"rs1308478111","consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485524,"feature_type":"variation","strand":1,"end":140485524,"alleles":["C","A"]},{"strand":1,"feature_type":"variation","end":140485525,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140485525,"source":"dbSNP","seq_region_name":"7","id":"rs906249993","clinical_significance":[]},{"seq_region_name":"7","id":"rs759691914","clinical_significance":[],"start":140485525,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","alleles":["AAAA","AA"],"end":140485528,"strand":1,"feature_type":"variation"},{"end":140485526,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140485526,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1213337036"},{"id":"rs1795333480","seq_region_name":"7","clinical_significance":[],"start":140485529,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","alleles":["G","T"],"end":140485529,"strand":1,"feature_type":"variation"},{"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485534,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140485534,"clinical_significance":[],"seq_region_name":"7","id":"rs1795333504"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1352264738","feature_type":"variation","strand":1,"end":140485538,"alleles":["C","T"],"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485538},{"seq_region_name":"7","id":"rs1340520244","clinical_significance":[],"strand":1,"feature_type":"variation","end":140485542,"alleles":["G","C","T"],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140485542,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140485546,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485546,"clinical_significance":[],"id":"rs918766151","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1294413406","end":140485550,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140485550,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1563102953","seq_region_name":"7","source":"dbSNP","start":140485553,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140485553,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140485554,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140485554,"source":"dbSNP","seq_region_name":"7","id":"rs1414920794","clinical_significance":[]},{"start":140485555,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","end":140485555,"alleles":["A","C"],"strand":1,"feature_type":"variation","id":"rs1795333686","seq_region_name":"7","clinical_significance":[]},{"id":"rs955696368","seq_region_name":"7","clinical_significance":[],"end":140485556,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","start":140485556,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant"},{"seq_region_name":"7","id":"rs1795333741","clinical_significance":[],"alleles":["T","C"],"end":140485557,"strand":1,"feature_type":"variation","start":140485557,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant"},{"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140485560,"source":"dbSNP","strand":1,"feature_type":"variation","end":140485560,"alleles":["A","G"],"seq_region_name":"7","id":"rs139680508","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140485562,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485562,"clinical_significance":[],"seq_region_name":"7","id":"rs1376692916"},{"start":140485563,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","alleles":["T","C"],"end":140485563,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795333809","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795333826","source":"dbSNP","start":140485564,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","end":140485564,"alleles":["A","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1300754404","source":"dbSNP","start":140485566,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","end":140485566,"alleles":["T","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795333867","feature_type":"variation","strand":1,"end":140485574,"alleles":["A","C"],"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485574},{"alleles":["C","A"],"end":140485575,"feature_type":"variation","strand":1,"source":"dbSNP","start":140485575,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1465176924"},{"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485577,"feature_type":"variation","strand":1,"end":140485577,"alleles":["G","C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1354911909"},{"id":"rs1795333969","seq_region_name":"7","clinical_significance":[],"end":140485581,"alleles":["AAAA","AAA"],"strand":1,"feature_type":"variation","start":140485578,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant"},{"source":"dbSNP","start":140485583,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","end":140485583,"alleles":["T","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1476714550"},{"seq_region_name":"7","id":"rs1222004960","clinical_significance":[],"start":140485584,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","alleles":["T","G"],"end":140485584,"strand":1,"feature_type":"variation"},{"end":140485585,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140485585,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795334579"},{"seq_region_name":"7","id":"rs1188537037","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C","T"],"end":140485587,"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140485587,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["A","C","T"],"end":140485591,"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140485591,"source":"dbSNP","seq_region_name":"7","id":"rs1795334625","clinical_significance":[]},{"alleles":["T","A"],"end":140485596,"feature_type":"variation","strand":1,"source":"dbSNP","start":140485596,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795334651"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140485597,"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140485597,"source":"dbSNP","seq_region_name":"7","id":"rs4726826","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563102966","source":"dbSNP","start":140485601,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","end":140485602,"alleles":["AG","-"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795334861","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140485602,"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140485602,"source":"dbSNP"},{"start":140485606,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","end":140485606,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs911441886","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140485609,"alleles":["T","G"],"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485609,"clinical_significance":[],"id":"rs1795334912","seq_region_name":"7"},{"start":140485610,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","end":140485610,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs567128426","seq_region_name":"7","clinical_significance":[]},{"end":140485612,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140485612,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","seq_region_name":"7","id":"rs1795334966","clinical_significance":[]},{"seq_region_name":"7","id":"rs1245853789","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140485614,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140485614},{"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140485618,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140485618,"seq_region_name":"7","id":"rs1294263573","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1481048192","feature_type":"variation","strand":1,"end":140485620,"alleles":["AG","-"],"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485619},{"source":"dbSNP","start":140485621,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140485621,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130400432"},{"source":"dbSNP","start":140485629,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140485629,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795335043"},{"end":140485631,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140485631,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","id":"rs1795335073","seq_region_name":"7","clinical_significance":[]},{"end":140485632,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140485632,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","seq_region_name":"7","id":"rs1253278412","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140485635,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485635,"clinical_significance":[],"id":"rs1202917384","seq_region_name":"7"},{"start":140485636,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","end":140485636,"alleles":["T","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795335143","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140485638,"source":"dbSNP","strand":1,"feature_type":"variation","end":140485638,"alleles":["T","C"],"seq_region_name":"7","id":"rs1489907033","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140485640,"source":"dbSNP","strand":1,"feature_type":"variation","end":140485640,"alleles":["G","C"],"seq_region_name":"7","id":"rs1221847699","clinical_significance":[]},{"seq_region_name":"7","id":"rs1317658584","clinical_significance":[],"strand":1,"feature_type":"variation","end":140485641,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140485641,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1795335251","seq_region_name":"7","source":"dbSNP","start":140485644,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140485644,"feature_type":"variation","strand":1},{"alleles":["T","A","C"],"end":140485645,"feature_type":"variation","strand":1,"source":"dbSNP","start":140485645,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs979120104"},{"id":"rs1298544300","seq_region_name":"7","clinical_significance":[],"start":140485648,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","alleles":["A","C"],"end":140485648,"strand":1,"feature_type":"variation"},{"start":140485650,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","end":140485650,"alleles":["A","G"],"strand":1,"feature_type":"variation","id":"rs1274376675","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1235641575","alleles":["A","C"],"end":140485652,"feature_type":"variation","strand":1,"source":"dbSNP","start":140485652,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs374733852","clinical_significance":[],"strand":1,"feature_type":"variation","end":140485659,"alleles":["G","GG"],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140485659,"source":"dbSNP"},{"end":140485660,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140485660,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585513229"},{"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485662,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140485662,"clinical_significance":[],"seq_region_name":"7","id":"rs1585513233"},{"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140485663,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140485663,"id":"rs1321069939","seq_region_name":"7","clinical_significance":[]},{"start":140485664,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","alleles":["G","T"],"end":140485664,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1309891600","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795335513","source":"dbSNP","start":140485679,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","end":140485679,"alleles":["C","A"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140485680,"alleles":["C","T"],"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485680,"clinical_significance":[],"id":"rs888177239","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs924931450","consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485682,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140485682},{"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140485685,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CA","-"],"end":140485686,"seq_region_name":"7","id":"rs1585513248","clinical_significance":[]},{"alleles":["T","C"],"end":140485690,"feature_type":"variation","strand":1,"source":"dbSNP","start":140485690,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795335588","seq_region_name":"7"},{"alleles":["TTGTTG","TTG"],"end":140485698,"strand":1,"feature_type":"variation","start":140485693,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","id":"rs1299491691","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140485694,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","end":140485694,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs561081335","seq_region_name":"7"},{"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485695,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140485695,"clinical_significance":[],"id":"rs1463910281","seq_region_name":"7"},{"start":140485696,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","end":140485696,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs1399208920","seq_region_name":"7","clinical_significance":[]},{"id":"rs1481939457","seq_region_name":"7","clinical_significance":[],"start":140485700,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","alleles":["T","C"],"end":140485700,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1005693565","clinical_significance":[],"alleles":["A","T"],"end":140485702,"strand":1,"feature_type":"variation","start":140485702,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant"},{"seq_region_name":"7","id":"rs1015456108","clinical_significance":[],"start":140485706,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","alleles":["A","G"],"end":140485706,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140485711,"source":"dbSNP","strand":1,"feature_type":"variation","end":140485711,"alleles":["C","A","T"],"id":"rs1795336102","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs140792548","end":140485715,"alleles":["AAAA","AAAAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140485712,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["C","CC"],"end":140485716,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485716,"clinical_significance":[],"seq_region_name":"7","id":"rs761325490"},{"end":140485716,"alleles":["C","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140485716,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs766061014"},{"seq_region_name":"7","id":"rs1585513271","clinical_significance":[],"strand":1,"feature_type":"variation","end":140485719,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140485719,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1187000883","end":140485720,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140485720,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140485721,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","end":140485721,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs935105041"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585513283","source":"dbSNP","start":140485722,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140485722,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1176951824","alleles":["G","A"],"end":140485723,"feature_type":"variation","strand":1,"source":"dbSNP","start":140485723,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs746764678","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140485724,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140485724},{"end":140485725,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140485725,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs768220886"},{"strand":1,"feature_type":"variation","end":140485726,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140485726,"source":"dbSNP","seq_region_name":"7","id":"rs113363597","clinical_significance":[]},{"start":140485729,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","end":140485729,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795336526","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795336564","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140485732,"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140485732,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795336586","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140485734,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140485734},{"strand":1,"feature_type":"variation","end":140485735,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140485735,"source":"dbSNP","id":"rs1585513295","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs896327321","source":"dbSNP","start":140485737,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","end":140485737,"alleles":["C","T"],"feature_type":"variation","strand":1},{"start":140485738,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","alleles":["G","A","C"],"end":140485738,"strand":1,"feature_type":"variation","id":"rs998141569","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140485739,"alleles":["C","T"],"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485739,"clinical_significance":[],"seq_region_name":"7","id":"rs1795336721"},{"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140485741,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140485741,"seq_region_name":"7","id":"rs1795336743","clinical_significance":[]},{"clinical_significance":[],"id":"rs1383014087","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140485743,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485743},{"start":140485746,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","alleles":["T","C"],"end":140485746,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585513308","clinical_significance":[]},{"id":"rs1795336833","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140485747,"source":"dbSNP","strand":1,"feature_type":"variation","end":140485747,"alleles":["C","T"]},{"start":140485748,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","alleles":["C","T"],"end":140485748,"strand":1,"feature_type":"variation","id":"rs1243481254","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140485752,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140485752,"seq_region_name":"7","id":"rs1316960780","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs9648845","consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485753,"feature_type":"variation","strand":1,"alleles":["G","A","C","T"],"end":140485753},{"clinical_significance":[],"id":"rs954035565","seq_region_name":"7","consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485754,"feature_type":"variation","strand":1,"end":140485754,"alleles":["C","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs540188802","consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485756,"feature_type":"variation","strand":1,"end":140485756,"alleles":["T","C","G"]},{"seq_region_name":"7","id":"rs1585513333","clinical_significance":[],"alleles":["T","G"],"end":140485757,"strand":1,"feature_type":"variation","start":140485757,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585513336","alleles":["C","T"],"end":140485765,"feature_type":"variation","strand":1,"source":"dbSNP","start":140485765,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1045006345","alleles":["C","A","T"],"end":140485774,"feature_type":"variation","strand":1,"source":"dbSNP","start":140485774,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140485775,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140485775,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs905148820"},{"source":"dbSNP","start":140485781,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140485781,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1162565572"},{"strand":1,"feature_type":"variation","end":140485786,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140485786,"source":"dbSNP","seq_region_name":"7","id":"rs1795337191","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs762370095","source":"dbSNP","start":140485790,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","end":140485790,"alleles":["G","A"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140485791,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AA","-"],"end":140485792,"seq_region_name":"7","id":"rs1795337256","clinical_significance":[]},{"start":140485793,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","alleles":["T","C"],"end":140485793,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs149359669","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795337313","clinical_significance":[],"end":140485794,"alleles":["-","A"],"strand":1,"feature_type":"variation","start":140485795,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1016929640","alleles":["G","A"],"end":140485801,"feature_type":"variation","strand":1,"source":"dbSNP","start":140485801,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38"},{"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485804,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140485804,"clinical_significance":[],"id":"rs957501888","seq_region_name":"7"},{"seq_region_name":"7","id":"rs530211859","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140485805,"source":"dbSNP","strand":1,"feature_type":"variation","end":140485805,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1795337457","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140485813,"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140485813,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1195970691","clinical_significance":[],"start":140485815,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","alleles":["C","A"],"end":140485815,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs770303450","seq_region_name":"7","source":"dbSNP","start":140485817,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140485817,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140485829,"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140485829,"source":"dbSNP","seq_region_name":"7","id":"rs62490456","clinical_significance":[]},{"alleles":["G","A"],"end":140485832,"feature_type":"variation","strand":1,"source":"dbSNP","start":140485832,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795337721"},{"clinical_significance":[],"seq_region_name":"7","id":"rs182865058","consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485834,"feature_type":"variation","strand":1,"end":140485834,"alleles":["C","G","T"]},{"end":140485835,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140485835,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","seq_region_name":"7","id":"rs1795337800","clinical_significance":[]},{"seq_region_name":"7","id":"rs116297340","clinical_significance":[],"end":140485837,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140485837,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1485924891","source":"dbSNP","start":140485838,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","end":140485838,"alleles":["A","C"],"feature_type":"variation","strand":1},{"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485840,"feature_type":"variation","strand":1,"end":140485840,"alleles":["T","C"],"clinical_significance":[],"id":"rs1261901908","seq_region_name":"7"},{"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485841,"feature_type":"variation","strand":1,"end":140485841,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1273994466"},{"end":140485842,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140485842,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","seq_region_name":"7","id":"rs2130400700","clinical_significance":[]},{"source":"dbSNP","start":140485843,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","alleles":["CAACAGAGAAAGAGTAATTCA","CA"],"end":140485863,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1312575252"},{"clinical_significance":[],"seq_region_name":"7","id":"rs76244767","source":"dbSNP","start":140485847,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","alleles":["AGAGA","A","AGAGAGAGA"],"end":140485851,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140485847,"source":"dbSNP","strand":1,"feature_type":"variation","end":140485856,"alleles":["AGAGAAAGAG","AGAG"],"seq_region_name":"7","id":"rs1303684483","clinical_significance":[]},{"clinical_significance":[],"id":"rs1585513379","seq_region_name":"7","alleles":["G","A","C"],"end":140485848,"feature_type":"variation","strand":1,"source":"dbSNP","start":140485848,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38"},{"id":"rs927518586","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["AGAAAGA","AGA"],"end":140485855,"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140485849,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585513383","source":"dbSNP","start":140485850,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","end":140485850,"alleles":["G","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795338224","feature_type":"variation","strand":1,"end":140485854,"alleles":["G","A"],"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485854},{"clinical_significance":[],"id":"rs1795338245","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","T"],"end":140485855,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485855},{"clinical_significance":[],"seq_region_name":"7","id":"rs955587517","end":140485856,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140485856,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140485857,"source":"dbSNP","strand":1,"feature_type":"variation","end":140485857,"alleles":["T","C"],"seq_region_name":"7","id":"rs1795338290","clinical_significance":[]},{"seq_region_name":"7","id":"rs987400367","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140485858,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140485858},{"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485863,"feature_type":"variation","strand":1,"end":140485863,"alleles":["A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1322847596"},{"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485865,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140485865,"clinical_significance":[],"seq_region_name":"7","id":"rs1795338375"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795338394","source":"dbSNP","start":140485866,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","end":140485866,"alleles":["C","T"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140485870,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485870,"clinical_significance":[],"seq_region_name":"7","id":"rs937691334"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1275503941","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140485872,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485872},{"clinical_significance":[],"seq_region_name":"7","id":"rs1296491874","source":"dbSNP","start":140485874,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","end":140485874,"alleles":["G","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1419170356","clinical_significance":[],"strand":1,"feature_type":"variation","end":140485879,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140485879,"source":"dbSNP"},{"alleles":["C","T"],"end":140485880,"feature_type":"variation","strand":1,"source":"dbSNP","start":140485880,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1018429454"},{"clinical_significance":[],"seq_region_name":"7","id":"rs548388154","feature_type":"variation","strand":1,"end":140485881,"alleles":["G","A"],"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485881},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140485882,"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140485882,"source":"dbSNP","seq_region_name":"7","id":"rs979676420","clinical_significance":[]},{"source":"dbSNP","start":140485884,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","end":140485884,"alleles":["A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795338643"},{"seq_region_name":"7","id":"rs1795338669","clinical_significance":[],"start":140485886,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","end":140485886,"alleles":["A","C","T"],"strand":1,"feature_type":"variation"},{"end":140485888,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140485888,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","id":"rs1795338698","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485889,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140485889,"clinical_significance":[],"seq_region_name":"7","id":"rs1377380906"},{"clinical_significance":[],"seq_region_name":"7","id":"rs941151987","end":140485893,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140485893,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38"},{"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485894,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140485894,"clinical_significance":[],"id":"rs1232830871","seq_region_name":"7"},{"start":140485898,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","end":140485898,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1430753070","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140485899,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TAT","T"],"end":140485901,"seq_region_name":"7","id":"rs1261636952","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140485901,"alleles":["T","C"],"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485901,"clinical_significance":[],"seq_region_name":"7","id":"rs1037185591"},{"clinical_significance":[],"id":"rs1487657365","seq_region_name":"7","consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485904,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140485904},{"feature_type":"variation","strand":1,"end":140485906,"alleles":["C","G","T"],"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485906,"clinical_significance":[],"id":"rs924941308","seq_region_name":"7"},{"source":"dbSNP","start":140485910,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140485910,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795338962","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795338990","consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485912,"feature_type":"variation","strand":1,"end":140485912,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs1563103052","clinical_significance":[],"start":140485915,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","end":140485920,"alleles":["CTCCTG","-"],"strand":1,"feature_type":"variation"},{"alleles":["T","C"],"end":140485916,"feature_type":"variation","strand":1,"source":"dbSNP","start":140485916,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs896993104"},{"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140485917,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140485917,"id":"rs1795339074","seq_region_name":"7","clinical_significance":[]},{"id":"rs1273969680","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140485922,"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140485922,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795339135","clinical_significance":[],"start":140485923,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","alleles":["G","A"],"end":140485923,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1241683702","clinical_significance":[],"start":140485924,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","end":140485924,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140485926,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140485926,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795339179"},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140485928,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485928,"clinical_significance":[],"id":"rs997984765","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795339248","clinical_significance":[],"end":140485941,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140485941,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant"},{"feature_type":"variation","strand":1,"end":140485945,"alleles":["A","G"],"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485945,"clinical_significance":[],"seq_region_name":"7","id":"rs1795339279"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1328200664","end":140485948,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140485948,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs934949277","clinical_significance":[],"end":140485950,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140485950,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant"},{"strand":1,"feature_type":"variation","end":140485952,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140485952,"source":"dbSNP","id":"rs1585513422","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795339350","consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485959,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140485959},{"alleles":["G","A"],"end":140485960,"feature_type":"variation","strand":1,"source":"dbSNP","start":140485960,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795339367"},{"start":140485962,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","alleles":["G","C"],"end":140485962,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs62490457","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1315042407","consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485963,"feature_type":"variation","strand":1,"end":140485963,"alleles":["C","A","G","T"]},{"source":"dbSNP","start":140485964,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","end":140485964,"alleles":["G","A","C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs548787132","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140485964,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GGGGG","GGGGGG"],"end":140485968,"seq_region_name":"7","id":"rs1168817666","clinical_significance":[]},{"alleles":["G","C"],"end":140485968,"feature_type":"variation","strand":1,"source":"dbSNP","start":140485968,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1476590050"},{"source":"dbSNP","start":140485969,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","end":140485969,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs937853238"},{"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485970,"feature_type":"variation","strand":1,"end":140485970,"alleles":["A","C","G"],"clinical_significance":[],"id":"rs1010361099","seq_region_name":"7"},{"seq_region_name":"7","id":"rs957594763","clinical_significance":[],"strand":1,"feature_type":"variation","end":140485975,"alleles":["GGGGG","GGGGGG"],"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140485971,"source":"dbSNP"},{"seq_region_name":"7","id":"rs554051026","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140485973,"source":"dbSNP","strand":1,"feature_type":"variation","end":140485973,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1225524051","consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140485975,"feature_type":"variation","strand":1,"end":140485975,"alleles":["G","A"]},{"strand":1,"feature_type":"variation","end":140485991,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140485991,"source":"dbSNP","seq_region_name":"7","id":"rs917634341","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795339782","source":"dbSNP","start":140485999,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140485999,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1407745732","feature_type":"variation","strand":1,"end":140486000,"alleles":["T","C"],"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486000},{"clinical_significance":[],"id":"rs1795339814","seq_region_name":"7","feature_type":"variation","strand":1,"end":140486001,"alleles":["T","A"],"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486001},{"source":"dbSNP","start":140486006,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140486006,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs375265909","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1169077311","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140486007,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486007},{"seq_region_name":"7","id":"rs1020289627","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140486008,"source":"dbSNP","strand":1,"feature_type":"variation","end":140486008,"alleles":["T","C"]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140486016,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486016,"clinical_significance":[],"seq_region_name":"7","id":"rs1795339891"},{"seq_region_name":"7","id":"rs1795339912","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140486020,"source":"dbSNP","strand":1,"feature_type":"variation","end":140486020,"alleles":["T","C"]},{"end":140486022,"alleles":["CC","C"],"strand":1,"feature_type":"variation","start":140486021,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","seq_region_name":"7","id":"rs1440398796","clinical_significance":[]},{"id":"rs1795339976","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140486023,"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140486023,"source":"dbSNP"},{"end":140486024,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140486024,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","seq_region_name":"7","id":"rs1795339998","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs187492904","alleles":["G","A"],"end":140486026,"feature_type":"variation","strand":1,"source":"dbSNP","start":140486026,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38"},{"end":140486031,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140486031,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795340084","seq_region_name":"7"},{"start":140486032,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","alleles":["G","A"],"end":140486032,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs190813223","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795340142","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140486034,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140486034},{"seq_region_name":"7","id":"rs1196203243","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140486036,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140486036},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140486038,"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140486038,"source":"dbSNP","seq_region_name":"7","id":"rs1319713399","clinical_significance":[]},{"start":140486042,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","alleles":["C","A","G"],"end":140486042,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs538791823","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140486046,"alleles":["T","A"],"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486046,"clinical_significance":[],"id":"rs1356177691","seq_region_name":"7"},{"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486050,"feature_type":"variation","strand":1,"end":140486050,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs146306330"},{"clinical_significance":[],"seq_region_name":"7","id":"rs959013951","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140486052,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486052},{"start":140486056,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","end":140486056,"alleles":["G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1445895824","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs985438324","feature_type":"variation","strand":1,"end":140486070,"alleles":["GGGGG","GGGG"],"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486066},{"start":140486068,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","alleles":["G","A"],"end":140486068,"strand":1,"feature_type":"variation","id":"rs1329752773","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795340364","source":"dbSNP","start":140486071,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","end":140486071,"alleles":["C","T"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140486074,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","end":140486074,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs909588566"},{"id":"rs533561841","seq_region_name":"7","clinical_significance":[],"start":140486076,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","end":140486076,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140486078,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","end":140486078,"alleles":["A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1452241721","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795340483","clinical_significance":[],"strand":1,"feature_type":"variation","end":140486083,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140486083,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795340514","source":"dbSNP","start":140486084,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","end":140486084,"alleles":["T","C"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140486085,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140486085,"source":"dbSNP","seq_region_name":"7","id":"rs940985006","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795340587","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140486091,"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140486091,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1462371199","clinical_significance":[],"strand":1,"feature_type":"variation","end":140486093,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140486093,"source":"dbSNP"},{"id":"rs1795340620","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140486096,"source":"dbSNP","strand":1,"feature_type":"variation","end":140486096,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795340651","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140486103,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486103},{"end":140486104,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140486104,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","seq_region_name":"7","id":"rs1563103080","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140486108,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486108,"clinical_significance":[],"seq_region_name":"7","id":"rs555104915"},{"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140486109,"source":"dbSNP","strand":1,"feature_type":"variation","end":140486109,"alleles":["T","G"],"seq_region_name":"7","id":"rs1795340757","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795340780","clinical_significance":[],"alleles":["C","T"],"end":140486111,"strand":1,"feature_type":"variation","start":140486111,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs62490458","alleles":["G","A","C"],"end":140486115,"feature_type":"variation","strand":1,"source":"dbSNP","start":140486115,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1795340927","seq_region_name":"7","alleles":["G","A"],"end":140486127,"feature_type":"variation","strand":1,"source":"dbSNP","start":140486127,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38"},{"end":140486130,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140486130,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs183744759"},{"clinical_significance":[],"id":"rs994553971","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140486131,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486131},{"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140486134,"assembly_name":"GRCh38","consequence_type":"splice_region_variant","start":140486134,"source":"dbSNP","seq_region_name":"7","id":"rs1471506936","clinical_significance":[]},{"seq_region_name":"7","id":"rs1236590165","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"splice_region_variant","start":140486135,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140486135},{"alleles":["T","G"],"end":140486137,"strand":1,"feature_type":"variation","start":140486137,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_acceptor_variant","seq_region_name":"7","id":"rs1795341067","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140486139,"assembly_name":"GRCh38","consequence_type":"splice_region_variant","start":140486139,"source":"dbSNP","seq_region_name":"7","id":"rs1795341094","clinical_significance":[]},{"consequence_type":"splice_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486140,"feature_type":"variation","strand":1,"alleles":["A","C","T"],"end":140486140,"clinical_significance":[],"id":"rs1182018512","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1458947434","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140486141,"consequence_type":"splice_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486141},{"alleles":["A","C"],"end":140486150,"strand":1,"feature_type":"variation","start":140486150,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_polypyrimidine_tract_variant","seq_region_name":"7","id":"rs1795341185","clinical_significance":[]},{"end":140486152,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140486152,"consequence_type":"splice_polypyrimidine_tract_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795341209","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs62490459","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486155,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140486155},{"id":"rs1050939856","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486158,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140486158},{"alleles":["T","C","G"],"end":140486159,"feature_type":"variation","strand":1,"source":"dbSNP","start":140486159,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1335453069"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1006844091","source":"dbSNP","start":140486160,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140486160,"alleles":["C","G","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs554077147","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486161,"source":"dbSNP","strand":1,"feature_type":"variation","end":140486161,"alleles":["T","A"]},{"strand":1,"feature_type":"variation","end":140486168,"alleles":["TTTTTTTT","TTTT","TTTTTTT","TTTTTTTTT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486161,"source":"dbSNP","seq_region_name":"7","id":"rs889612582","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486168,"source":"dbSNP","strand":1,"feature_type":"variation","end":140486168,"alleles":["T","C"],"id":"rs1375163490","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140486176,"alleles":["TTTTTTT","TTTTTTTT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486170,"clinical_significance":[],"seq_region_name":"7","id":"rs1331166797"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1008302780","alleles":["G","A"],"end":140486183,"feature_type":"variation","strand":1,"source":"dbSNP","start":140486183,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["G","C"],"end":140486184,"strand":1,"feature_type":"variation","start":140486184,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795341607","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130401109","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486188,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140486188},{"id":"rs1261719031","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486189,"source":"dbSNP","strand":1,"feature_type":"variation","end":140486189,"alleles":["A","AA"]},{"strand":1,"feature_type":"variation","end":140486191,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486191,"source":"dbSNP","seq_region_name":"7","id":"rs369508772","clinical_significance":[]},{"seq_region_name":"7","id":"rs572855413","clinical_significance":[],"end":140486192,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140486192,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140486195,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140486195,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795341712"},{"id":"rs1001125291","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486196,"source":"dbSNP","strand":1,"feature_type":"variation","end":140486196,"alleles":["T","C","G"]},{"seq_region_name":"7","id":"rs778890817","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486199,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140486199},{"clinical_significance":[],"seq_region_name":"7","id":"rs1403121921","source":"dbSNP","start":140486200,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140486200,"alleles":["G","A","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1032565671","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486202,"feature_type":"variation","strand":1,"end":140486202,"alleles":["T","C","G"]},{"seq_region_name":"7","id":"rs1585513593","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486203,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140486203},{"clinical_significance":[],"id":"rs1243511953","seq_region_name":"7","source":"dbSNP","start":140486207,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140486207,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1177848267","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486208,"source":"dbSNP","strand":1,"feature_type":"variation","end":140486208,"alleles":["A","G"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486211,"feature_type":"variation","strand":1,"end":140486211,"alleles":["T","A"],"clinical_significance":[],"id":"rs1474190486","seq_region_name":"7"},{"id":"rs1468724520","seq_region_name":"7","clinical_significance":[],"start":140486215,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140486215,"alleles":["T","G"],"strand":1,"feature_type":"variation"},{"start":140486221,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140486221,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs956377065","clinical_significance":[]},{"seq_region_name":"7","id":"rs988234852","clinical_significance":[],"alleles":["T","A"],"end":140486222,"strand":1,"feature_type":"variation","start":140486222,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1185437973","clinical_significance":[],"start":140486224,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140486224,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486225,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140486225,"id":"rs62492360","seq_region_name":"7","clinical_significance":[]},{"start":140486226,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140486226,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795342266","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795342289","alleles":["T","A","C"],"end":140486228,"feature_type":"variation","strand":1,"source":"dbSNP","start":140486228,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1795342315","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140486229,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486229,"source":"dbSNP"},{"source":"dbSNP","start":140486231,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140486231,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs970923832"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486232,"feature_type":"variation","strand":1,"end":140486232,"alleles":["G","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs564852499"},{"clinical_significance":[],"id":"rs1308765750","seq_region_name":"7","feature_type":"variation","strand":1,"end":140486233,"alleles":["G","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486233},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486236,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140486236,"clinical_significance":[],"seq_region_name":"7","id":"rs1034512485"},{"seq_region_name":"7","id":"rs1795342475","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486237,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140486237},{"seq_region_name":"7","id":"rs1795342503","clinical_significance":[],"strand":1,"feature_type":"variation","end":140486241,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486241,"source":"dbSNP"},{"start":140486242,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C","G"],"end":140486242,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795342538","clinical_significance":[]},{"start":140486244,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140486244,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1370124868","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795342557","source":"dbSNP","start":140486249,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140486249,"alleles":["A","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs577922901","clinical_significance":[],"strand":1,"feature_type":"variation","end":140486253,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486253,"source":"dbSNP"},{"end":140486256,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140486256,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795342649"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140486259,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486259,"source":"dbSNP","seq_region_name":"7","id":"rs1585513628","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140486263,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486263,"clinical_significance":[],"id":"rs941842608","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs985061602","feature_type":"variation","strand":1,"end":140486264,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486264},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486267,"feature_type":"variation","strand":1,"end":140486267,"alleles":["T","C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795342757"},{"feature_type":"variation","strand":1,"end":140486274,"alleles":["G","C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486274,"clinical_significance":[],"seq_region_name":"7","id":"rs1037602367"},{"clinical_significance":[],"id":"rs1420981895","seq_region_name":"7","alleles":["T","TGTAT"],"end":140486277,"feature_type":"variation","strand":1,"source":"dbSNP","start":140486277,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140486277,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486277,"source":"dbSNP","seq_region_name":"7","id":"rs1795342821","clinical_significance":[]},{"alleles":["A","G"],"end":140486278,"feature_type":"variation","strand":1,"source":"dbSNP","start":140486278,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs919201370"},{"feature_type":"variation","strand":1,"end":140486285,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486285,"clinical_significance":[],"seq_region_name":"7","id":"rs1795342892"},{"seq_region_name":"7","id":"rs1358276409","clinical_significance":[],"start":140486285,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140486287,"alleles":["CCC","CC"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140486287,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486287,"source":"dbSNP","seq_region_name":"7","id":"rs545177891","clinical_significance":[]},{"alleles":["G","A"],"end":140486288,"feature_type":"variation","strand":1,"source":"dbSNP","start":140486288,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1457590091"},{"id":"rs146120624","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140486295,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486295,"source":"dbSNP"},{"alleles":["G","A","C","T"],"end":140486296,"feature_type":"variation","strand":1,"source":"dbSNP","start":140486296,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1426926313"},{"seq_region_name":"7","id":"rs1795343077","clinical_significance":[],"end":140486305,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140486305,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140486311,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140486311,"alleles":["G","-"],"strand":1,"feature_type":"variation","id":"rs1319969165","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486314,"feature_type":"variation","strand":1,"alleles":["TTAGTT","TT"],"end":140486319,"clinical_significance":[],"seq_region_name":"7","id":"rs972369575"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1328428505","source":"dbSNP","start":140486315,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140486315,"feature_type":"variation","strand":1},{"end":140486316,"alleles":["-","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140486317,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795343183"},{"clinical_significance":[],"seq_region_name":"7","id":"rs73480302","feature_type":"variation","strand":1,"end":140486317,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486317},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140486321,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486321,"source":"dbSNP","seq_region_name":"7","id":"rs1487338152","clinical_significance":[]},{"source":"dbSNP","start":140486323,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140486323,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1285611274"},{"start":140486324,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140486324,"strand":1,"feature_type":"variation","id":"rs548323023","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140486325,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486325,"source":"dbSNP","seq_region_name":"7","id":"rs1795343339","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140486327,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486327,"source":"dbSNP","seq_region_name":"7","id":"rs2130401273","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1269739452","source":"dbSNP","start":140486329,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140486329,"alleles":["A","G"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486330,"source":"dbSNP","strand":1,"feature_type":"variation","end":140486330,"alleles":["C","T"],"seq_region_name":"7","id":"rs1008728804","clinical_significance":[]},{"start":140486331,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140486331,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1039773476","clinical_significance":[]},{"seq_region_name":"7","id":"rs900013726","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486334,"source":"dbSNP","strand":1,"feature_type":"variation","end":140486334,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1218991471","clinical_significance":[],"strand":1,"feature_type":"variation","end":140486345,"alleles":["TGT","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486343,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486344,"source":"dbSNP","strand":1,"feature_type":"variation","end":140486344,"alleles":["G","C"],"seq_region_name":"7","id":"rs1363350231","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486347,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140486347,"id":"rs1280612805","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140486348,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486348,"source":"dbSNP","seq_region_name":"7","id":"rs1346209329","clinical_significance":[]},{"seq_region_name":"7","id":"rs573926529","clinical_significance":[],"end":140486350,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140486350,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1358017576","end":140486352,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140486352,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1225935985","seq_region_name":"7","alleles":["G","A","C"],"end":140486353,"feature_type":"variation","strand":1,"source":"dbSNP","start":140486353,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795343672","clinical_significance":[],"alleles":["A","T"],"end":140486358,"strand":1,"feature_type":"variation","start":140486358,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130401327","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486365,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140486365},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486368,"feature_type":"variation","strand":1,"end":140486368,"alleles":["C","T"],"clinical_significance":[],"id":"rs1281967177","seq_region_name":"7"},{"alleles":["C","T"],"end":140486370,"strand":1,"feature_type":"variation","start":140486370,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585513705","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486374,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140486374,"id":"rs1795343758","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1360524714","source":"dbSNP","start":140486376,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140486376,"feature_type":"variation","strand":1},{"start":140486377,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140486377,"strand":1,"feature_type":"variation","id":"rs1795343813","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1173777952","clinical_significance":[],"strand":1,"feature_type":"variation","end":140486378,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486378,"source":"dbSNP"},{"start":140486390,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140486390,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795343863","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1001011088","end":140486394,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140486394,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140486397,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140486397,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795343918"},{"seq_region_name":"7","id":"rs1032492096","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140486406,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486406,"source":"dbSNP"},{"alleles":["G","C"],"end":140486409,"strand":1,"feature_type":"variation","start":140486409,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795343964","clinical_significance":[]},{"seq_region_name":"7","id":"rs1420203728","clinical_significance":[],"start":140486410,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140486410,"strand":1,"feature_type":"variation"},{"start":140486411,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140486411,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585513725","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140486413,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486413,"source":"dbSNP","id":"rs62492361","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140486414,"alleles":["T","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486414,"clinical_significance":[],"seq_region_name":"7","id":"rs986541887"},{"source":"dbSNP","start":140486415,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140486415,"alleles":["C","A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs542891391"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140486418,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486418,"clinical_significance":[],"id":"rs1214602453","seq_region_name":"7"},{"source":"dbSNP","start":140486420,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140486420,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795344209","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1484392197","alleles":["G","C"],"end":140486425,"feature_type":"variation","strand":1,"source":"dbSNP","start":140486425,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140486432,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140486432,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs62492362"},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140486436,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486436,"source":"dbSNP","id":"rs1795344320","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486437,"source":"dbSNP","strand":1,"feature_type":"variation","end":140486437,"alleles":["C","T"],"id":"rs1795344339","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140486438,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486438,"source":"dbSNP","seq_region_name":"7","id":"rs1585513745","clinical_significance":[]},{"seq_region_name":"7","id":"rs1209906347","clinical_significance":[],"end":140486449,"alleles":["GCTG","G"],"strand":1,"feature_type":"variation","start":140486446,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140486449,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140486449,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1308422630"},{"clinical_significance":[],"id":"rs1795344439","seq_region_name":"7","source":"dbSNP","start":140486450,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140486450,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795344457","clinical_significance":[],"start":140486451,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140486451,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1585513748","seq_region_name":"7","feature_type":"variation","strand":1,"end":140486456,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486456},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486458,"feature_type":"variation","strand":1,"end":140486458,"alleles":["G","A","C"],"clinical_significance":[],"id":"rs1260574554","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140486460,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486460,"source":"dbSNP","id":"rs1795344486","seq_region_name":"7","clinical_significance":[]},{"start":140486460,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["CACCCGCCACC","-"],"end":140486470,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795344510","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585513752","clinical_significance":[],"alleles":["A","C"],"end":140486461,"strand":1,"feature_type":"variation","start":140486461,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140486462,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140486462,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs552283967","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140486464,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486464,"clinical_significance":[],"id":"rs1277085006","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486465,"source":"dbSNP","strand":1,"feature_type":"variation","end":140486465,"alleles":["G","A"],"seq_region_name":"7","id":"rs570498775","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130401442","clinical_significance":[],"alleles":["C","G"],"end":140486466,"strand":1,"feature_type":"variation","start":140486466,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795344602","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486470,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140486470},{"strand":1,"feature_type":"variation","alleles":["C","A","G","T"],"end":140486472,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486472,"source":"dbSNP","id":"rs537893145","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140486473,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486473,"source":"dbSNP","seq_region_name":"7","id":"rs1196583961","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795344679","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486474,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140486474},{"feature_type":"variation","strand":1,"end":140486476,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486476,"clinical_significance":[],"id":"rs893017529","seq_region_name":"7"},{"end":140486478,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140486478,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1172740909","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486482,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140486482,"seq_region_name":"7","id":"rs1422809127","clinical_significance":[]},{"alleles":["TTTTTTT","TTTTTTTT"],"end":140486489,"feature_type":"variation","strand":1,"source":"dbSNP","start":140486483,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1463944250"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795344770","feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140486484,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486484},{"clinical_significance":[],"id":"rs980942865","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140486486,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486486},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486499,"source":"dbSNP","strand":1,"feature_type":"variation","end":140486499,"alleles":["G","A"],"seq_region_name":"7","id":"rs945947109","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140486502,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486502,"clinical_significance":[],"id":"rs1563103152","seq_region_name":"7"},{"end":140486506,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140486506,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1205268786"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486507,"source":"dbSNP","strand":1,"feature_type":"variation","end":140486507,"alleles":["G","A","T"],"id":"rs764842880","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585513774","end":140486511,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140486511,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486514,"feature_type":"variation","strand":1,"end":140486514,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs963082781"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795344936","alleles":["G","A"],"end":140486515,"feature_type":"variation","strand":1,"source":"dbSNP","start":140486515,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1563103164","clinical_significance":[],"alleles":["C","T"],"end":140486516,"strand":1,"feature_type":"variation","start":140486516,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs556438185","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486520,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140486520},{"start":140486524,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140486524,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs973239850","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585513781","clinical_significance":[],"strand":1,"feature_type":"variation","end":140486534,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486534,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486543,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140486543,"clinical_significance":[],"id":"rs1795345060","seq_region_name":"7"},{"id":"rs1563103168","seq_region_name":"7","clinical_significance":[],"start":140486549,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140486549,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1197132151","end":140486553,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140486553,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486554,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140486554,"clinical_significance":[],"seq_region_name":"7","id":"rs1795345093"},{"strand":1,"feature_type":"variation","end":140486557,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486557,"source":"dbSNP","seq_region_name":"7","id":"rs1317904742","clinical_significance":[]},{"id":"rs1795345134","seq_region_name":"7","clinical_significance":[],"end":140486558,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140486558,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs919085347","feature_type":"variation","strand":1,"end":140486562,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486562},{"end":140486566,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140486566,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1002951803","clinical_significance":[]},{"end":140486567,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140486567,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1322950609"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795345242","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486572,"feature_type":"variation","strand":1,"end":140486572,"alleles":["C","T"]},{"source":"dbSNP","start":140486574,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140486574,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1310182353"},{"source":"dbSNP","start":140486581,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140486581,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1034356988"},{"clinical_significance":[],"id":"rs1377386078","seq_region_name":"7","feature_type":"variation","strand":1,"end":140486582,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486582},{"clinical_significance":[],"id":"rs1795345314","seq_region_name":"7","source":"dbSNP","start":140486583,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140486583,"alleles":["G","A"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140486585,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486585,"clinical_significance":[],"id":"rs894651036","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs73482205","source":"dbSNP","start":140486588,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140486588,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs2130401549","clinical_significance":[],"strand":1,"feature_type":"variation","end":140486593,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486593,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486594,"source":"dbSNP","strand":1,"feature_type":"variation","end":140486594,"alleles":["A","C"],"seq_region_name":"7","id":"rs535784523","clinical_significance":[]},{"end":140486599,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140486599,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795345423","seq_region_name":"7"},{"id":"rs1399506026","seq_region_name":"7","clinical_significance":[],"start":140486601,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140486601,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1795345453","clinical_significance":[],"strand":1,"feature_type":"variation","end":140486613,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486613,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1294015648","clinical_significance":[],"start":140486619,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140486619,"strand":1,"feature_type":"variation"},{"id":"rs774721068","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140486623,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486623,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795345531","clinical_significance":[],"start":140486624,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140486624,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486625,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140486625,"seq_region_name":"7","id":"rs1795345548","clinical_significance":[]},{"alleles":["T","C"],"end":140486626,"feature_type":"variation","strand":1,"source":"dbSNP","start":140486626,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795345566","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795345577","end":140486629,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140486629,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795345595","end":140486630,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140486630,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140486632,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486632,"source":"dbSNP","seq_region_name":"7","id":"rs1795345616","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140486633,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486633,"clinical_significance":[],"seq_region_name":"7","id":"rs1585513815"},{"end":140486636,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140486636,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs62492363"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140486639,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486639,"clinical_significance":[],"seq_region_name":"7","id":"rs560295833"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140486642,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486642,"source":"dbSNP","seq_region_name":"7","id":"rs1795345665","clinical_significance":[]},{"seq_region_name":"7","id":"rs62492364","clinical_significance":[],"start":140486644,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140486644,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs972297384","clinical_significance":[],"start":140486645,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140486645,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1795345755","clinical_significance":[],"end":140486649,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140486649,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1025349958","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486651,"feature_type":"variation","strand":1,"end":140486651,"alleles":["T","C"]},{"alleles":["A","C"],"end":140486653,"feature_type":"variation","strand":1,"source":"dbSNP","start":140486653,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795345794"},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140486656,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486656,"clinical_significance":[],"seq_region_name":"7","id":"rs1795345803"},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140486666,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486666,"source":"dbSNP","seq_region_name":"7","id":"rs1177205758","clinical_significance":[]},{"start":140486669,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","T"],"end":140486669,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs954984098","clinical_significance":[]},{"id":"rs1795345865","seq_region_name":"7","clinical_significance":[],"start":140486670,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140486671,"alleles":["TT","T"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140486677,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140486677,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795345881"},{"clinical_significance":[],"id":"rs1795345906","seq_region_name":"7","end":140486678,"alleles":["A","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140486678,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140486680,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486680,"clinical_significance":[],"seq_region_name":"7","id":"rs1585513852"},{"seq_region_name":"7","id":"rs1039828978","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140486684,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486684,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795345991","clinical_significance":[],"start":140486685,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140486685,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140486686,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486686,"clinical_significance":[],"seq_region_name":"7","id":"rs899941364"},{"clinical_significance":[],"id":"rs571363547","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486690,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140486690},{"id":"rs1263108492","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140486695,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486695,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1243411090","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486699,"source":"dbSNP","strand":1,"feature_type":"variation","end":140486699,"alleles":["A","G"]},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140486701,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486701,"clinical_significance":[],"seq_region_name":"7","id":"rs1354051088"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1310954602","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486702,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140486702},{"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140486706,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486706,"source":"dbSNP","seq_region_name":"7","id":"rs942574995","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486708,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140486708,"clinical_significance":[],"seq_region_name":"7","id":"rs1795346135"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795346157","feature_type":"variation","strand":1,"end":140486712,"alleles":["C","A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486712},{"strand":1,"feature_type":"variation","end":140486720,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486720,"source":"dbSNP","id":"rs1795346171","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1053998596","alleles":["G","A"],"end":140486722,"feature_type":"variation","strand":1,"source":"dbSNP","start":140486722,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140486724,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140486726,"alleles":["TCT","T"],"strand":1,"feature_type":"variation","id":"rs1348942053","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1388685290","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486727,"source":"dbSNP","strand":1,"feature_type":"variation","end":140486727,"alleles":["G","A"]},{"id":"rs532569031","seq_region_name":"7","clinical_significance":[],"end":140486732,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140486732,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs914385245","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486733,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140486733},{"source":"dbSNP","start":140486738,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140486738,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1362746588"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486739,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140486739,"seq_region_name":"7","id":"rs1292080607","clinical_significance":[]},{"clinical_significance":[],"id":"rs945976168","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140486740,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486740},{"strand":1,"feature_type":"variation","end":140486742,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486742,"source":"dbSNP","seq_region_name":"7","id":"rs1010242571","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795346334","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486746,"source":"dbSNP","strand":1,"feature_type":"variation","end":140486746,"alleles":["A","G"]},{"end":140486747,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140486747,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs866285845"},{"strand":1,"feature_type":"variation","end":140486748,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486748,"source":"dbSNP","seq_region_name":"7","id":"rs1795346382","clinical_significance":[]},{"seq_region_name":"7","id":"rs1201669250","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140486749,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486749,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140486754,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486754,"source":"dbSNP","seq_region_name":"7","id":"rs1795346421","clinical_significance":[]},{"seq_region_name":"7","id":"rs1432009954","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140486764,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486764,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140486766,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486766,"source":"dbSNP","id":"rs1795346456","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795346471","end":140486769,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140486769,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140486774,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486774,"source":"dbSNP","id":"rs1490720513","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1267264120","clinical_significance":[],"start":140486777,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140486777,"alleles":["T","TT"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1795346532","clinical_significance":[],"start":140486780,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140486780,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1221140110","source":"dbSNP","start":140486785,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140486785,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1488317699","seq_region_name":"7","feature_type":"variation","strand":1,"end":140486802,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486802},{"seq_region_name":"7","id":"rs1287742799","clinical_significance":[],"start":140486803,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140486803,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140486806,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486806,"source":"dbSNP","seq_region_name":"7","id":"rs1563103205","clinical_significance":[]},{"source":"dbSNP","start":140486807,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140486807,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs928679590"},{"id":"rs1219620198","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140486809,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486809,"source":"dbSNP"},{"start":140486810,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140486810,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795346821","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486816,"feature_type":"variation","strand":1,"end":140486816,"alleles":["T","C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1267549020"},{"source":"dbSNP","start":140486817,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140486817,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs938677754"},{"seq_region_name":"7","id":"rs2130401746","clinical_significance":[],"end":140486820,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140486820,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486826,"source":"dbSNP","strand":1,"feature_type":"variation","end":140486826,"alleles":["C","A","G"],"id":"rs1795346862","seq_region_name":"7","clinical_significance":[]},{"end":140486829,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140486829,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585513910","clinical_significance":[]},{"start":140486831,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140486831,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1235138027","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140486832,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486832,"source":"dbSNP","seq_region_name":"7","id":"rs1055912261","clinical_significance":[]},{"seq_region_name":"7","id":"rs1483373222","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486838,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140486838},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486840,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140486840,"seq_region_name":"7","id":"rs1400716160","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1342409403","alleles":["G","A"],"end":140486843,"feature_type":"variation","strand":1,"source":"dbSNP","start":140486843,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486844,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140486844,"seq_region_name":"7","id":"rs906212014","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140486847,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486847,"clinical_significance":[],"seq_region_name":"7","id":"rs1795347002"},{"source":"dbSNP","start":140486849,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140486849,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1001851946","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140486850,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486850,"source":"dbSNP","id":"rs1033295594","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140486853,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140486853,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs151335585"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140486857,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486857,"source":"dbSNP","seq_region_name":"7","id":"rs1361891939","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1419269745","feature_type":"variation","strand":1,"end":140486858,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486858},{"seq_region_name":"7","id":"rs1469470771","clinical_significance":[],"alleles":["T","G"],"end":140486863,"strand":1,"feature_type":"variation","start":140486863,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795347123","clinical_significance":[],"alleles":["T","G"],"end":140486868,"strand":1,"feature_type":"variation","start":140486868,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["TCTCTCTCT","TCTCTCT"],"end":140486876,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486868,"clinical_significance":[],"seq_region_name":"7","id":"rs1795347136"},{"seq_region_name":"7","id":"rs1795347151","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486871,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140486871},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486878,"source":"dbSNP","strand":1,"feature_type":"variation","end":140486878,"alleles":["T","C"],"id":"rs973122742","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","C"],"end":140486884,"feature_type":"variation","strand":1,"source":"dbSNP","start":140486884,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795347206","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140486887,"alleles":["T","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486887,"clinical_significance":[],"id":"rs1795347231","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1174743343","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486892,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140486892},{"feature_type":"variation","strand":1,"end":140486896,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486896,"clinical_significance":[],"seq_region_name":"7","id":"rs1795347282"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486899,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140486899,"seq_region_name":"7","id":"rs760798339","clinical_significance":[]},{"end":140486902,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140486902,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585513936","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1006281968","feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140486903,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486903},{"seq_region_name":"7","id":"rs189120353","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140486904,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486904,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795347434","clinical_significance":[],"start":140486908,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140486908,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1377601955","source":"dbSNP","start":140486910,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140486910,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1426714127","clinical_significance":[],"start":140486913,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140486913,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1795347512","clinical_significance":[],"end":140486923,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140486923,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795347533","alleles":["G","A"],"end":140486924,"feature_type":"variation","strand":1,"source":"dbSNP","start":140486924,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["T","G"],"end":140486925,"feature_type":"variation","strand":1,"source":"dbSNP","start":140486925,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795347557"},{"alleles":["G","C"],"end":140486929,"feature_type":"variation","strand":1,"source":"dbSNP","start":140486929,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795347585"},{"seq_region_name":"7","id":"rs1194965552","clinical_significance":[],"start":140486937,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140486937,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1477878909","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140486941,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486941,"source":"dbSNP"},{"alleles":["C","G"],"end":140486944,"strand":1,"feature_type":"variation","start":140486944,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs192174342","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486947,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140486947,"clinical_significance":[],"seq_region_name":"7","id":"rs1191080286"},{"clinical_significance":[],"id":"rs1038288199","seq_region_name":"7","feature_type":"variation","strand":1,"end":140486951,"alleles":["AA","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486950},{"alleles":["C","T"],"end":140486952,"strand":1,"feature_type":"variation","start":140486952,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795347935","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140486955,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486955,"source":"dbSNP","seq_region_name":"7","id":"rs184488703","clinical_significance":[]},{"id":"rs987804638","seq_region_name":"7","clinical_significance":[],"start":140486962,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140486962,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486966,"source":"dbSNP","strand":1,"feature_type":"variation","end":140486966,"alleles":["G","A"],"seq_region_name":"7","id":"rs911789038","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486971,"feature_type":"variation","strand":1,"end":140486971,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795348090"},{"seq_region_name":"7","id":"rs1342554208","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486972,"source":"dbSNP","strand":1,"feature_type":"variation","end":140486972,"alleles":["A","G"]},{"start":140486973,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140486973,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795348145","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1262467314","end":140486974,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140486974,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486974,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CAAAAATACAAAAAT","CAAAAAT"],"end":140486988,"seq_region_name":"7","id":"rs1795348200","clinical_significance":[]},{"id":"rs1219095505","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140486975,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140486975},{"alleles":["A","C"],"end":140486978,"strand":1,"feature_type":"variation","start":140486978,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs993751467","clinical_significance":[]},{"alleles":["AAAAA","AAAAAA"],"end":140486987,"feature_type":"variation","strand":1,"source":"dbSNP","start":140486983,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1365024305"},{"feature_type":"variation","strand":1,"end":140486987,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486987,"clinical_significance":[],"id":"rs1276453157","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140486992,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140486992,"clinical_significance":[],"seq_region_name":"7","id":"rs943262135"},{"source":"dbSNP","start":140486993,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140486993,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1399479112"},{"source":"dbSNP","start":140486998,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140486998,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs975439529","seq_region_name":"7"},{"end":140487000,"alleles":["ATG","-"],"strand":1,"feature_type":"variation","start":140486998,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1341334669","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs921257383","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140487003,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487003},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487004,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GTGTGTGT","GTGTGT"],"end":140487011,"seq_region_name":"7","id":"rs369408229","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487006,"feature_type":"variation","strand":1,"end":140487006,"alleles":["G","A"],"clinical_significance":[],"id":"rs1172015548","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1467588801","end":140487007,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140487007,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1795351304","seq_region_name":"7","clinical_significance":[],"alleles":["G","T"],"end":140487008,"strand":1,"feature_type":"variation","start":140487008,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1334455209","alleles":["T","C"],"end":140487013,"feature_type":"variation","strand":1,"source":"dbSNP","start":140487013,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1167967795","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487015,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140487015},{"end":140487017,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140487017,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1441946384","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140487019,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487019,"clinical_significance":[],"seq_region_name":"7","id":"rs1795351395"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140487023,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487023,"source":"dbSNP","id":"rs750314277","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795351590","clinical_significance":[],"start":140487025,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140487025,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1795351608","clinical_significance":[],"alleles":["C","T"],"end":140487029,"strand":1,"feature_type":"variation","start":140487029,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140487040,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140487040,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1361236949","clinical_significance":[]},{"end":140487047,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140487047,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585513995"},{"id":"rs1440490272","seq_region_name":"7","clinical_significance":[],"alleles":["A","G"],"end":140487049,"strand":1,"feature_type":"variation","start":140487049,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1242247368","seq_region_name":"7","alleles":["C","A"],"end":140487051,"feature_type":"variation","strand":1,"source":"dbSNP","start":140487051,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1243299536","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140487052,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487052},{"seq_region_name":"7","id":"rs1290469203","clinical_significance":[],"start":140487053,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140487053,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487054,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140487054,"clinical_significance":[],"seq_region_name":"7","id":"rs1795351730"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487060,"source":"dbSNP","strand":1,"feature_type":"variation","end":140487060,"alleles":["C","A","T"],"seq_region_name":"7","id":"rs1339441589","clinical_significance":[]},{"source":"dbSNP","start":140487061,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140487061,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs187124279"},{"id":"rs1459091574","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140487063,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487063,"source":"dbSNP"},{"source":"dbSNP","start":140487072,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140487072,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1248360850"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795351823","source":"dbSNP","start":140487073,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","-"],"end":140487073,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487079,"feature_type":"variation","strand":1,"end":140487079,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs547555827"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140487081,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487081,"source":"dbSNP","seq_region_name":"7","id":"rs751406742","clinical_significance":[]},{"seq_region_name":"7","id":"rs1188004688","clinical_significance":[],"strand":1,"feature_type":"variation","end":140487084,"alleles":["G","C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487084,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487088,"feature_type":"variation","strand":1,"end":140487088,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795351876"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1244743077","end":140487091,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140487091,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["C","A","G","T"],"end":140487093,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487093,"clinical_significance":[],"seq_region_name":"7","id":"rs1446735757"},{"seq_region_name":"7","id":"rs945542241","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487094,"source":"dbSNP","strand":1,"feature_type":"variation","end":140487094,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585514019","end":140487102,"alleles":["A","C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140487102,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795352001","clinical_significance":[],"strand":1,"feature_type":"variation","end":140487103,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487103,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1286203836","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140487110,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487110,"source":"dbSNP"},{"seq_region_name":"7","id":"rs59857834","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487122,"source":"dbSNP","strand":1,"feature_type":"variation","end":140487122,"alleles":["G","A","C"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487123,"source":"dbSNP","strand":1,"feature_type":"variation","end":140487123,"alleles":["C","A"],"seq_region_name":"7","id":"rs977344276","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1255836914","source":"dbSNP","start":140487127,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140487127,"alleles":["A","G"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140487131,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487131,"clinical_significance":[],"seq_region_name":"7","id":"rs1795352115"},{"source":"dbSNP","start":140487138,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140487138,"alleles":["C","A","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs906816033"},{"clinical_significance":[],"id":"rs1384798425","seq_region_name":"7","feature_type":"variation","strand":1,"end":140487139,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487139},{"clinical_significance":[],"id":"rs112857604","seq_region_name":"7","feature_type":"variation","strand":1,"end":140487144,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487144},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487144,"feature_type":"variation","strand":1,"alleles":["C","-"],"end":140487144,"clinical_significance":[],"seq_region_name":"7","id":"rs1462581226"},{"end":140487145,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140487145,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1408897144","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487145,"source":"dbSNP","strand":1,"feature_type":"variation","end":140487150,"alleles":["AAAAAA","AAAAAAA"],"seq_region_name":"7","id":"rs1795352226","clinical_significance":[]},{"id":"rs938707544","seq_region_name":"7","clinical_significance":[],"end":140487146,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140487146,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["A","G"],"end":140487147,"strand":1,"feature_type":"variation","start":140487147,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130402040","clinical_significance":[]},{"start":140487151,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140487151,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795352272","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795352289","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487154,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140487154},{"strand":1,"feature_type":"variation","end":140487163,"alleles":["AAATAAA","AAA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487157,"source":"dbSNP","seq_region_name":"7","id":"rs1795352306","clinical_significance":[]},{"source":"dbSNP","start":140487173,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140487173,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795352325"},{"strand":1,"feature_type":"variation","end":140487178,"alleles":["AAAAAA","AAAAAAA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487173,"source":"dbSNP","seq_region_name":"7","id":"rs1394968589","clinical_significance":[]},{"clinical_significance":[],"id":"rs61672202","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487176,"feature_type":"variation","strand":1,"end":140487194,"alleles":["AAACAAACAAACAAACAAA","AAACAAACAAACAAA","AAACAAACAAACAAACAAACAAA","AAACAAACAAACAAACAAACAAACAAA"]},{"source":"dbSNP","start":140487178,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140487178,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1409887476"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487179,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140487179,"seq_region_name":"7","id":"rs1179070895","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487182,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140487182,"seq_region_name":"7","id":"rs1795352461","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795352477","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140487183,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487183,"source":"dbSNP"},{"clinical_significance":[],"id":"rs942115776","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487184,"feature_type":"variation","strand":1,"end":140487184,"alleles":["A","C"]},{"seq_region_name":"7","id":"rs2130402081","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487188,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AAA","AA"],"end":140487190},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487189,"feature_type":"variation","strand":1,"alleles":["A","C","T"],"end":140487189,"clinical_significance":[],"seq_region_name":"7","id":"rs751368588"},{"strand":1,"feature_type":"variation","end":140487191,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487191,"source":"dbSNP","id":"rs1795352555","seq_region_name":"7","clinical_significance":[]},{"alleles":["AAAAA","AAAA"],"end":140487196,"strand":1,"feature_type":"variation","start":140487192,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130402093","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1452257662","end":140487200,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140487200,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1585514063","seq_region_name":"7","end":140487206,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140487206,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs898033567","seq_region_name":"7","clinical_significance":[],"alleles":["AAAAAAA","AAAAAA","AAAAAAAA"],"end":140487212,"strand":1,"feature_type":"variation","start":140487206,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140487207,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C","G"],"end":140487207,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs754868377","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140487209,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487209,"source":"dbSNP","seq_region_name":"7","id":"rs1359075687","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140487211,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487211,"clinical_significance":[],"seq_region_name":"7","id":"rs58941533"},{"source":"dbSNP","start":140487214,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140487214,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1242796404","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1375095670","clinical_significance":[],"start":140487217,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140487217,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"id":"rs541778845","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140487219,"strand":1,"feature_type":"variation","start":140487219,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140487221,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140487221,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs890732522","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795353124","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487235,"feature_type":"variation","strand":1,"end":140487235,"alleles":["A","G"]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140487236,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487236,"clinical_significance":[],"seq_region_name":"7","id":"rs1563103285"},{"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140487243,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487243,"source":"dbSNP","seq_region_name":"7","id":"rs55840736","clinical_significance":[]},{"start":140487244,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140487244,"strand":1,"feature_type":"variation","id":"rs1026032950","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795353215","clinical_significance":[],"start":140487248,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140487248,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795353228","source":"dbSNP","start":140487255,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AAA","AA"],"end":140487257,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1325032212","alleles":["A","G"],"end":140487257,"feature_type":"variation","strand":1,"source":"dbSNP","start":140487257,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140487258,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140487258,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795353261"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487260,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140487260,"id":"rs560275534","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs950625836","source":"dbSNP","start":140487262,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140487262,"alleles":["A","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795353331","source":"dbSNP","start":140487263,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140487263,"alleles":["T","C"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140487265,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487265,"source":"dbSNP","seq_region_name":"7","id":"rs61401494","clinical_significance":[]},{"clinical_significance":[],"id":"rs10253030","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","A","C","G"],"end":140487274,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487274},{"seq_region_name":"7","id":"rs2130402179","clinical_significance":[],"alleles":["A","G"],"end":140487275,"strand":1,"feature_type":"variation","start":140487275,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1011782164","clinical_significance":[],"end":140487277,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140487277,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795353503","clinical_significance":[],"alleles":["T","C"],"end":140487281,"strand":1,"feature_type":"variation","start":140487281,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585514111","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140487292,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487292},{"clinical_significance":[],"seq_region_name":"7","id":"rs1204208146","source":"dbSNP","start":140487294,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140487294,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1021367607","clinical_significance":[],"strand":1,"feature_type":"variation","end":140487295,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487295,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs964656797","source":"dbSNP","start":140487298,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140487298,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs536578983","feature_type":"variation","strand":1,"end":140487299,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487299},{"id":"rs201458857","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140487300,"strand":1,"feature_type":"variation","start":140487300,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140487301,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487301,"clinical_significance":[],"seq_region_name":"7","id":"rs531696293"},{"seq_region_name":"7","id":"rs550109134","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487302,"source":"dbSNP","strand":1,"feature_type":"variation","end":140487302,"alleles":["G","A"]},{"source":"dbSNP","start":140487302,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140487303,"alleles":["GG","GGG"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795353690"},{"seq_region_name":"7","id":"rs928447925","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487303,"source":"dbSNP","strand":1,"feature_type":"variation","end":140487303,"alleles":["G","A"]},{"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140487304,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487304,"source":"dbSNP","seq_region_name":"7","id":"rs1585514142","clinical_significance":[]},{"source":"dbSNP","start":140487305,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140487305,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1287047389"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585514146","end":140487307,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140487307,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1218985128","clinical_significance":[],"strand":1,"feature_type":"variation","end":140487309,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487309,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140487311,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487311,"clinical_significance":[],"seq_region_name":"7","id":"rs13247786"},{"seq_region_name":"7","id":"rs7810075","clinical_significance":[],"strand":1,"feature_type":"variation","end":140487316,"alleles":["A","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487316,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1220169331","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487321,"feature_type":"variation","strand":1,"end":140487321,"alleles":["C","T"]},{"id":"rs1461964252","seq_region_name":"7","clinical_significance":[],"start":140487322,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140487322,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795353966","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140487332,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487332},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140487335,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487335,"source":"dbSNP","seq_region_name":"7","id":"rs1273556199","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795354015","clinical_significance":[],"alleles":["G","A"],"end":140487336,"strand":1,"feature_type":"variation","start":140487336,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs915898848","seq_region_name":"7","source":"dbSNP","start":140487337,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140487337,"feature_type":"variation","strand":1},{"end":140487338,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140487338,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs537807247"},{"feature_type":"variation","strand":1,"alleles":["CC","CCC"],"end":140487339,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487338,"clinical_significance":[],"seq_region_name":"7","id":"rs66794008"},{"id":"rs7802945","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140487339,"strand":1,"feature_type":"variation","start":140487339,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs386718468","feature_type":"variation","strand":1,"end":140487340,"alleles":["CA","TG"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487339},{"source":"dbSNP","start":140487340,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140487340,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs7810087","seq_region_name":"7"},{"end":140487340,"alleles":["A","TG"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140487340,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1554452850"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1343061430","feature_type":"variation","strand":1,"end":140487343,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487343},{"source":"dbSNP","start":140487344,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140487344,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs938266527"},{"seq_region_name":"7","id":"rs191889814","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487345,"source":"dbSNP","strand":1,"feature_type":"variation","end":140487345,"alleles":["G","A"]},{"feature_type":"variation","strand":1,"end":140487348,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487348,"clinical_significance":[],"id":"rs2130402312","seq_region_name":"7"},{"start":140487349,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140487349,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1427208789","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585514197","clinical_significance":[],"end":140487350,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140487350,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140487354,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140487354,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1189357562","seq_region_name":"7"},{"end":140487356,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140487356,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs929481328","clinical_significance":[]},{"clinical_significance":[],"id":"rs1563103327","seq_region_name":"7","source":"dbSNP","start":140487357,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140487357,"alleles":["A","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1383556971","source":"dbSNP","start":140487358,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140487358,"alleles":["G","A"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487359,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140487359,"clinical_significance":[],"seq_region_name":"7","id":"rs898845924"},{"start":140487361,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140487361,"strand":1,"feature_type":"variation","id":"rs1292896802","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795354750","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487365,"feature_type":"variation","strand":1,"end":140487365,"alleles":["A","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130402337","end":140487367,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140487367,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1795354778","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140487368,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487368,"source":"dbSNP"},{"id":"rs558386459","seq_region_name":"7","clinical_significance":[],"start":140487369,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","G","T"],"end":140487369,"strand":1,"feature_type":"variation"},{"alleles":["G","A"],"end":140487370,"strand":1,"feature_type":"variation","start":140487370,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1047829976","seq_region_name":"7","clinical_significance":[]},{"id":"rs1795354888","seq_region_name":"7","clinical_significance":[],"alleles":["A","T"],"end":140487373,"strand":1,"feature_type":"variation","start":140487373,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140487374,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487374,"source":"dbSNP","id":"rs1285139495","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140487375,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487375,"source":"dbSNP","seq_region_name":"7","id":"rs1795354949","clinical_significance":[]},{"end":140487377,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140487377,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs547648540"},{"clinical_significance":[],"seq_region_name":"7","id":"rs576968774","source":"dbSNP","start":140487379,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140487379,"alleles":["C","G","T"],"feature_type":"variation","strand":1},{"alleles":["T","G"],"end":140487380,"strand":1,"feature_type":"variation","start":140487380,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1018817540","seq_region_name":"7","clinical_significance":[]},{"id":"rs537951765","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487384,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140487384},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140487385,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487385,"source":"dbSNP","id":"rs996109985","seq_region_name":"7","clinical_significance":[]},{"start":140487386,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140487386,"strand":1,"feature_type":"variation","id":"rs1795355181","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs556095467","feature_type":"variation","strand":1,"end":140487389,"alleles":["T","C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487389},{"clinical_significance":[],"seq_region_name":"7","id":"rs574375604","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487390,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140487390},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487391,"source":"dbSNP","strand":1,"feature_type":"variation","end":140487391,"alleles":["G","A","C"],"seq_region_name":"7","id":"rs957256878","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1021354650","source":"dbSNP","start":140487392,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140487392,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487397,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140487397,"clinical_significance":[],"seq_region_name":"7","id":"rs542094585"},{"seq_region_name":"7","id":"rs1585514230","clinical_significance":[],"start":140487399,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140487399,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140487400,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140487400,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs199998403","seq_region_name":"7"},{"seq_region_name":"7","id":"rs966860766","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487401,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140487401},{"start":140487405,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140487405,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs982567995","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["ACTAAAAATACAAAAAATTAACTGGGCATGGTGGCATGCGCCTATAGTCCCAGTTACTCAGGAGGCTGAGGCA","ACTAAAAATACAAAAAATTAACTGGGCATGGTGGCATGCGCCTATAGTCCCAGTTACTCAGGAGGCTGAGGCACTAAAAATACAAAAAATTAACTGGGCATGGTGGCATGCGCCTATAGTCCCAGTTACTCAGGAGGCTGAGGCA"],"end":140487479,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487407,"clinical_significance":[],"seq_region_name":"7","id":"rs1795355625"},{"end":140487409,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140487409,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1419097581","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140487414,"alleles":["AAAAA","AAAA","AAAAAA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487410,"source":"dbSNP","id":"rs1479707186","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140487411,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487411,"source":"dbSNP","seq_region_name":"7","id":"rs928143189","clinical_significance":[]},{"alleles":["A","C","G"],"end":140487413,"strand":1,"feature_type":"variation","start":140487413,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs938151531","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140487417,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487417,"clinical_significance":[],"seq_region_name":"7","id":"rs1175884190"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1236033525","feature_type":"variation","strand":1,"end":140487423,"alleles":["AAAAAA","AAAAAAA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487418},{"end":140487419,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140487419,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs2130402434","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795355819","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487420,"source":"dbSNP","strand":1,"feature_type":"variation","end":140487420,"alleles":["A","G"]},{"alleles":["A","G"],"end":140487423,"strand":1,"feature_type":"variation","start":140487423,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1203420817","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487424,"feature_type":"variation","strand":1,"end":140487424,"alleles":["T","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795355866"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130402441","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487429,"feature_type":"variation","strand":1,"end":140487429,"alleles":["T","G"]},{"source":"dbSNP","start":140487431,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140487431,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1458659300"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487434,"feature_type":"variation","strand":1,"end":140487434,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1364726060"},{"alleles":["G","C"],"end":140487437,"strand":1,"feature_type":"variation","start":140487437,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1455069608","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487439,"feature_type":"variation","strand":1,"alleles":["GG","G"],"end":140487440,"clinical_significance":[],"id":"rs1795355983","seq_region_name":"7"},{"source":"dbSNP","start":140487441,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140487441,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795356008"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1035494474","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487442,"feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140487442},{"end":140487443,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140487443,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1055320482","clinical_significance":[]},{"end":140487445,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140487445,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs57074330","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs138032435","source":"dbSNP","start":140487446,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140487446,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795356223","source":"dbSNP","start":140487450,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140487450,"alleles":["A","G"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487451,"feature_type":"variation","strand":1,"end":140487451,"alleles":["T","C"],"clinical_significance":[],"id":"rs1795356238","seq_region_name":"7"},{"end":140487452,"alleles":["-","AG"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140487453,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1380867914"},{"seq_region_name":"7","id":"rs1795356290","clinical_significance":[],"strand":1,"feature_type":"variation","end":140487453,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487453,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140487455,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487455,"clinical_significance":[],"seq_region_name":"7","id":"rs1795356324"},{"id":"rs1304361323","seq_region_name":"7","clinical_significance":[],"start":140487456,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140487456,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487460,"feature_type":"variation","strand":1,"end":140487460,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1451600671"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487463,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140487463,"clinical_significance":[],"id":"rs1585514286","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140487464,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487464,"source":"dbSNP","seq_region_name":"7","id":"rs1795356432","clinical_significance":[]},{"start":140487466,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140487466,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs963735448","clinical_significance":[]},{"end":140487474,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140487474,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs554042485","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487477,"feature_type":"variation","strand":1,"end":140487477,"alleles":["G","A"],"clinical_significance":[],"id":"rs1460559622","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140487483,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487483,"source":"dbSNP","seq_region_name":"7","id":"rs1795356556","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487486,"source":"dbSNP","strand":1,"feature_type":"variation","end":140487486,"alleles":["T","C"],"id":"rs886101360","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487487,"feature_type":"variation","strand":1,"end":140487487,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585514299"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487488,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140487488,"clinical_significance":[],"seq_region_name":"7","id":"rs1008655993"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1318468387","feature_type":"variation","strand":1,"end":140487489,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487489},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487495,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140487495,"clinical_significance":[],"seq_region_name":"7","id":"rs1795356688"},{"source":"dbSNP","start":140487496,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140487496,"alleles":["C","A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1165769482"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487500,"feature_type":"variation","strand":1,"end":140487500,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1425841645"},{"clinical_significance":[],"seq_region_name":"7","id":"rs531658890","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487505,"feature_type":"variation","strand":1,"end":140487505,"alleles":["A","C","G"]},{"source":"dbSNP","start":140487508,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140487508,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1236567669"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487509,"feature_type":"variation","strand":1,"end":140487509,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795356820"},{"id":"rs1671821494","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487514,"source":"dbSNP","strand":1,"feature_type":"variation","end":140487514,"alleles":["A","G"]},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140487516,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487516,"source":"dbSNP","seq_region_name":"7","id":"rs1259211145","clinical_significance":[]},{"seq_region_name":"7","id":"rs1040500067","clinical_significance":[],"start":140487517,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140487517,"strand":1,"feature_type":"variation"},{"start":140487518,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140487518,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130402557","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487520,"feature_type":"variation","strand":1,"alleles":["C","A","G","T"],"end":140487520,"clinical_significance":[],"id":"rs1488055156","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487521,"feature_type":"variation","strand":1,"end":140487521,"alleles":["C","A","T"],"clinical_significance":[],"id":"rs1440679021","seq_region_name":"7"},{"start":140487522,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140487522,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1240597369","clinical_significance":[]},{"seq_region_name":"7","id":"rs1197227965","clinical_significance":[],"start":140487527,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140487527,"alleles":["C","A","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1479379549","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487528,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140487528},{"seq_region_name":"7","id":"rs1223333175","clinical_significance":[],"start":140487529,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C","G"],"end":140487529,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["CACTGCACT","CACT"],"end":140487540,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487532,"clinical_significance":[],"seq_region_name":"7","id":"rs1221654022"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487533,"feature_type":"variation","strand":1,"end":140487533,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130402585"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795357160","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487534,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140487534},{"seq_region_name":"7","id":"rs1323183575","clinical_significance":[],"start":140487536,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140487536,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1312430042","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487537,"source":"dbSNP","strand":1,"feature_type":"variation","end":140487537,"alleles":["C","T"]},{"id":"rs929386246","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140487538,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487538,"source":"dbSNP"},{"alleles":["C","A"],"end":140487541,"feature_type":"variation","strand":1,"source":"dbSNP","start":140487541,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795357416"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487543,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140487543,"id":"rs1795357438","seq_region_name":"7","clinical_significance":[]},{"end":140487547,"alleles":["-","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140487548,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130402611"},{"clinical_significance":[],"id":"rs1795357462","seq_region_name":"7","end":140487549,"alleles":["GG","GGG"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140487548,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140487548,"alleles":["-","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487549,"clinical_significance":[],"id":"rs1377307226","seq_region_name":"7"},{"source":"dbSNP","start":140487549,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140487549,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1311385414"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795357516","source":"dbSNP","start":140487549,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","GGGGACAGAGTG"],"end":140487549,"feature_type":"variation","strand":1},{"start":140487550,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140487550,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs184446089","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487550,"feature_type":"variation","strand":1,"alleles":["C","-"],"end":140487550,"clinical_significance":[],"seq_region_name":"7","id":"rs1490019733"},{"clinical_significance":[],"seq_region_name":"7","id":"rs4726830","alleles":["G","A","C"],"end":140487551,"feature_type":"variation","strand":1,"source":"dbSNP","start":140487551,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1795357618","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487553,"source":"dbSNP","strand":1,"feature_type":"variation","end":140487553,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1294265092","clinical_significance":[],"end":140487555,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140487555,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487557,"source":"dbSNP","strand":1,"feature_type":"variation","end":140487557,"alleles":["A","G"],"seq_region_name":"7","id":"rs1459483035","clinical_significance":[]},{"source":"dbSNP","start":140487560,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140487560,"alleles":["A","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1421270889"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140487563,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487563,"source":"dbSNP","seq_region_name":"7","id":"rs1379306977","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140487566,"alleles":["CTCT","CT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487563,"source":"dbSNP","seq_region_name":"7","id":"rs758789036","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795357738","feature_type":"variation","strand":1,"end":140487565,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487565},{"seq_region_name":"7","id":"rs1795357757","clinical_significance":[],"start":140487576,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140487576,"strand":1,"feature_type":"variation"},{"id":"rs1795357782","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487582,"source":"dbSNP","strand":1,"feature_type":"variation","end":140487582,"alleles":["A","C"]},{"seq_region_name":"7","id":"rs1795357806","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487583,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140487583},{"clinical_significance":[],"seq_region_name":"7","id":"rs1382493030","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487585,"feature_type":"variation","strand":1,"end":140487585,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs1795357849","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487592,"source":"dbSNP","strand":1,"feature_type":"variation","end":140487592,"alleles":["A","C"]},{"id":"rs1032834042","seq_region_name":"7","clinical_significance":[],"alleles":["A","G"],"end":140487594,"strand":1,"feature_type":"variation","start":140487594,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140487595,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487595,"clinical_significance":[],"seq_region_name":"7","id":"rs1795357989"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1419070441","source":"dbSNP","start":140487605,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140487605,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1795358021","seq_region_name":"7","source":"dbSNP","start":140487608,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140487614,"alleles":["TTGTTTT","TT"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140487627,"alleles":["TTGTTTTAATTGCTGTTGTT","TTGTTTTAATTGCTGTTGTTTTAATTGCTGTTGTT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487608,"source":"dbSNP","id":"rs1268627479","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140487619,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487619,"source":"dbSNP","seq_region_name":"7","id":"rs1191314694","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795358091","end":140487621,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140487621,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795358113","clinical_significance":[],"end":140487623,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140487623,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1585514376","seq_region_name":"7","end":140487625,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140487625,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140487628,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140487628,"alleles":["A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795358147"},{"end":140487631,"alleles":["T","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140487631,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs957311062"},{"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140487632,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487632,"clinical_significance":[],"seq_region_name":"7","id":"rs1010568324"},{"start":140487633,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140487633,"strand":1,"feature_type":"variation","id":"rs1795358217","seq_region_name":"7","clinical_significance":[]},{"end":140487635,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140487635,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795358233","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140487637,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487637,"source":"dbSNP","seq_region_name":"7","id":"rs1795358254","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487639,"source":"dbSNP","strand":1,"feature_type":"variation","end":140487639,"alleles":["G","A"],"seq_region_name":"7","id":"rs1354170844","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487642,"source":"dbSNP","strand":1,"feature_type":"variation","end":140487642,"alleles":["T","C"],"seq_region_name":"7","id":"rs1020958624","clinical_significance":[]},{"start":140487644,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140487644,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs529309287","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795358318","seq_region_name":"7","source":"dbSNP","start":140487645,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140487645,"feature_type":"variation","strand":1},{"id":"rs967077654","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140487649,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487649,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795358364","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487651,"source":"dbSNP","strand":1,"feature_type":"variation","end":140487651,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1563103399","clinical_significance":[],"alleles":["A","G"],"end":140487653,"strand":1,"feature_type":"variation","start":140487653,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487656,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140487656,"seq_region_name":"7","id":"rs1236610271","clinical_significance":[]},{"end":140487661,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140487661,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1335142044","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140487662,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487662,"clinical_significance":[],"seq_region_name":"7","id":"rs56160706"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795358450","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487667,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140487667},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487669,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140487669,"clinical_significance":[],"seq_region_name":"7","id":"rs1795358468"},{"start":140487670,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140487670,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs772486466","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130402758","source":"dbSNP","start":140487671,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140487671,"feature_type":"variation","strand":1},{"start":140487674,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140487674,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1363138029","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140487677,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487677,"clinical_significance":[],"seq_region_name":"7","id":"rs1399460799"},{"seq_region_name":"7","id":"rs2130402766","clinical_significance":[],"start":140487678,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140487678,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1795358536","clinical_significance":[],"start":140487680,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140487680,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"id":"rs1795358560","seq_region_name":"7","clinical_significance":[],"end":140487683,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140487683,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140487689,"alleles":["CCC","CCCC"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487687,"source":"dbSNP","seq_region_name":"7","id":"rs34249766","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585514409","clinical_significance":[],"start":140487691,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140487691,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487693,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140487693,"id":"rs1795358605","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs982230547","seq_region_name":"7","end":140487695,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140487695,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs946935871","clinical_significance":[],"start":140487697,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140487697,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1795358675","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487698,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140487698},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140487700,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487700,"clinical_significance":[],"seq_region_name":"7","id":"rs1298708521"},{"seq_region_name":"7","id":"rs775620715","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487708,"source":"dbSNP","strand":1,"feature_type":"variation","end":140487708,"alleles":["C","T"]},{"alleles":["C","T"],"end":140487712,"feature_type":"variation","strand":1,"source":"dbSNP","start":140487712,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1042716280"},{"seq_region_name":"7","id":"rs1795358766","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487713,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140487713},{"seq_region_name":"7","id":"rs1585514424","clinical_significance":[],"strand":1,"feature_type":"variation","end":140487719,"alleles":["GG","GGG"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487718,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140487720,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487720,"clinical_significance":[],"seq_region_name":"7","id":"rs1795358805"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1157231092","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487721,"feature_type":"variation","strand":1,"end":140487721,"alleles":["A","T"]},{"seq_region_name":"7","id":"rs928027224","clinical_significance":[],"end":140487722,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140487722,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140487724,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140487724,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1378739752"},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140487728,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487728,"source":"dbSNP","seq_region_name":"7","id":"rs1795358860","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795358874","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487731,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140487731},{"alleles":["G","T"],"end":140487735,"feature_type":"variation","strand":1,"source":"dbSNP","start":140487735,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130402829"},{"alleles":["A","G"],"end":140487737,"feature_type":"variation","strand":1,"source":"dbSNP","start":140487737,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1389477376"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487740,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140487740,"seq_region_name":"7","id":"rs959428598","clinical_significance":[]},{"id":"rs1035398040","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140487747,"strand":1,"feature_type":"variation","start":140487747,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["C","T"],"end":140487748,"strand":1,"feature_type":"variation","start":140487748,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795358959","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1198055076","end":140487752,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140487752,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140487756,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140487756,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1488452552","clinical_significance":[]},{"seq_region_name":"7","id":"rs1263373185","clinical_significance":[],"strand":1,"feature_type":"variation","end":140487758,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487758,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487761,"feature_type":"variation","strand":1,"end":140487761,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs760817935"},{"seq_region_name":"7","id":"rs1795359032","clinical_significance":[],"start":140487763,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140487763,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs990975666","source":"dbSNP","start":140487765,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140487765,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs920754032","seq_region_name":"7","alleles":["C","T"],"end":140487767,"feature_type":"variation","strand":1,"source":"dbSNP","start":140487767,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs548065561","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140487771,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487771,"source":"dbSNP"},{"start":140487772,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140487772,"strand":1,"feature_type":"variation","id":"rs1235248551","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487776,"feature_type":"variation","strand":1,"end":140487776,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs542601833"},{"clinical_significance":[],"id":"rs1795359145","seq_region_name":"7","alleles":["G","A"],"end":140487781,"feature_type":"variation","strand":1,"source":"dbSNP","start":140487781,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140487789,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140487789,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs907548625"},{"start":140487790,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140487790,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795359181","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1400657031","feature_type":"variation","strand":1,"end":140487792,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487792},{"clinical_significance":[],"seq_region_name":"7","id":"rs963342566","feature_type":"variation","strand":1,"end":140487803,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487803},{"id":"rs1795359301","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140487810,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487810,"source":"dbSNP"},{"source":"dbSNP","start":140487822,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140487822,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1316428797"},{"seq_region_name":"7","id":"rs1382038709","clinical_significance":[],"end":140487825,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140487825,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140487831,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140487831,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1403269323","clinical_significance":[]},{"id":"rs1305129444","seq_region_name":"7","clinical_significance":[],"start":140487833,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140487833,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1220881967","source":"dbSNP","start":140487839,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140487839,"alleles":["G","A"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140487841,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487841,"clinical_significance":[],"id":"rs1563103417","seq_region_name":"7"},{"seq_region_name":"7","id":"rs140036656","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487842,"source":"dbSNP","strand":1,"feature_type":"variation","end":140487851,"alleles":["AAGTTAAGTT","AAGTT"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487844,"source":"dbSNP","strand":1,"feature_type":"variation","end":140487844,"alleles":["G","C"],"id":"rs1429197974","seq_region_name":"7","clinical_significance":[]},{"start":140487846,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140487846,"alleles":["T","G"],"strand":1,"feature_type":"variation","id":"rs779032807","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1233979026","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487848,"source":"dbSNP","strand":1,"feature_type":"variation","end":140487848,"alleles":["A","C"]},{"seq_region_name":"7","id":"rs1026324057","clinical_significance":[],"start":140487849,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140487849,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140487851,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140487851,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs950695233"},{"source":"dbSNP","start":140487858,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140487858,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs944348537"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487861,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140487861,"clinical_significance":[],"seq_region_name":"7","id":"rs1795359779"},{"feature_type":"variation","strand":1,"end":140487869,"alleles":["TAAATAA","TAA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487863,"clinical_significance":[],"seq_region_name":"7","id":"rs1795359808"},{"seq_region_name":"7","id":"rs1190527322","clinical_significance":[],"alleles":["A","G"],"end":140487866,"strand":1,"feature_type":"variation","start":140487866,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["A","G"],"end":140487868,"strand":1,"feature_type":"variation","start":140487868,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795359867","clinical_significance":[]},{"id":"rs1040045653","seq_region_name":"7","clinical_significance":[],"start":140487873,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140487873,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs566329883","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140487876,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487876},{"alleles":["T","C"],"end":140487881,"feature_type":"variation","strand":1,"source":"dbSNP","start":140487881,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795359941"},{"source":"dbSNP","start":140487886,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140487886,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs764181149"},{"start":140487887,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140487887,"alleles":["T","-"],"strand":1,"feature_type":"variation","id":"rs1256667121","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487890,"source":"dbSNP","strand":1,"feature_type":"variation","end":140487890,"alleles":["A","G"],"seq_region_name":"7","id":"rs561227024","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795360052","end":140487907,"alleles":["ATGACATGA","ATGA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140487899,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795360070","clinical_significance":[],"start":140487905,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140487905,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140487911,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487911,"source":"dbSNP","seq_region_name":"7","id":"rs1795360102","clinical_significance":[]},{"start":140487913,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C","G"],"end":140487913,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs987589831","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487914,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140487914,"clinical_significance":[],"seq_region_name":"7","id":"rs1219349019"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795360206","source":"dbSNP","start":140487917,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140487921,"alleles":["AAAAA","AAAA"],"feature_type":"variation","strand":1},{"end":140487925,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140487925,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1341509216","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795360247","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140487927,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487927,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1795360267","seq_region_name":"7","feature_type":"variation","strand":1,"end":140487929,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487929},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795360279","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487930,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140487930},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487940,"feature_type":"variation","strand":1,"end":140487942,"alleles":["AAA","AA"],"clinical_significance":[],"id":"rs1481867540","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1268638529","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487945,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140487945},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140487948,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487948,"source":"dbSNP","seq_region_name":"7","id":"rs965271846","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130402986","end":140487954,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140487954,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs974957560","alleles":["A","G","T"],"end":140487956,"feature_type":"variation","strand":1,"source":"dbSNP","start":140487956,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140487957,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140487957,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs915366975","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140487959,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487959,"source":"dbSNP","seq_region_name":"7","id":"rs946997728","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795360418","clinical_significance":[],"start":140487964,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140487964,"strand":1,"feature_type":"variation"},{"id":"rs1795360440","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487970,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140487970},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487973,"feature_type":"variation","strand":1,"end":140487973,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs540144255"},{"end":140487974,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140487974,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795360477"},{"feature_type":"variation","strand":1,"end":140487975,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487975,"clinical_significance":[],"id":"rs1795360489","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1175915592","clinical_significance":[],"strand":1,"feature_type":"variation","end":140487979,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487979,"source":"dbSNP"},{"seq_region_name":"7","id":"rs776601970","clinical_significance":[],"start":140487980,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140487980,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140487981,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487981,"clinical_significance":[],"seq_region_name":"7","id":"rs1795360543"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487982,"feature_type":"variation","strand":1,"end":140487982,"alleles":["A","G"],"clinical_significance":[],"id":"rs900283342","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1563103437","clinical_significance":[],"start":140487985,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140487986,"alleles":["CC","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1237941093","clinical_significance":[],"strand":1,"feature_type":"variation","end":140487988,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140487988,"source":"dbSNP"},{"end":140487989,"alleles":["-","TA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140487990,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795360614"},{"feature_type":"variation","strand":1,"end":140487993,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487993,"clinical_significance":[],"seq_region_name":"7","id":"rs2130403028"},{"alleles":["CCC","CC"],"end":140487995,"strand":1,"feature_type":"variation","start":140487993,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1465721028","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140487994,"feature_type":"variation","strand":1,"end":140487994,"alleles":["C","T"],"clinical_significance":[],"id":"rs1795360660","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs931714184","alleles":["C","G","T"],"end":140487995,"feature_type":"variation","strand":1,"source":"dbSNP","start":140487995,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs761992916","clinical_significance":[],"strand":1,"feature_type":"variation","end":140488000,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488000,"source":"dbSNP"},{"end":140488003,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140488003,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795360726","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795360745","end":140488008,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140488008,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1795360764","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488011,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140488011},{"start":140488013,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140488013,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs551968139","clinical_significance":[]},{"id":"rs1054330866","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140488015,"strand":1,"feature_type":"variation","start":140488015,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140488016,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140488016,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795360826","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488018,"source":"dbSNP","strand":1,"feature_type":"variation","end":140488018,"alleles":["G","C"],"seq_region_name":"7","id":"rs1368651451","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488020,"source":"dbSNP","strand":1,"feature_type":"variation","end":140488020,"alleles":["T","A","C"],"seq_region_name":"7","id":"rs1795360858","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795360881","clinical_significance":[],"alleles":["G","T"],"end":140488022,"strand":1,"feature_type":"variation","start":140488022,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795360894","clinical_significance":[],"end":140488024,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140488024,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140488027,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140488027,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1185244815","clinical_significance":[]},{"end":140488030,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140488030,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs934318114","clinical_significance":[]},{"seq_region_name":"7","id":"rs1242487427","clinical_significance":[],"start":140488033,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140488033,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1795360954","clinical_significance":[],"alleles":["T","C"],"end":140488034,"strand":1,"feature_type":"variation","start":140488034,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1795360977","seq_region_name":"7","end":140488035,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140488035,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs2130403100","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488036,"source":"dbSNP","strand":1,"feature_type":"variation","end":140488036,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs1585514505","clinical_significance":[],"start":140488041,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A","C","G"],"end":140488041,"strand":1,"feature_type":"variation"},{"id":"rs1795361006","seq_region_name":"7","clinical_significance":[],"start":140488043,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140488043,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs892937531","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140488046,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488046},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488047,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140488047,"seq_region_name":"7","id":"rs1010164831","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140488050,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488050,"clinical_significance":[],"id":"rs1795361063","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1020590024","clinical_significance":[],"end":140488051,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140488051,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795361101","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140488053,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488053,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488054,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140488054,"seq_region_name":"7","id":"rs143176944","clinical_significance":[]},{"id":"rs576364769","seq_region_name":"7","clinical_significance":[],"start":140488055,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140488055,"strand":1,"feature_type":"variation"},{"alleles":["A","G"],"end":140488059,"feature_type":"variation","strand":1,"source":"dbSNP","start":140488059,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795361166"},{"alleles":["A","G"],"end":140488062,"strand":1,"feature_type":"variation","start":140488062,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1317402518","clinical_significance":[]},{"start":140488065,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140488065,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs2130403141","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795361197","clinical_significance":[],"strand":1,"feature_type":"variation","end":140488071,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488071,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488071,"feature_type":"variation","strand":1,"alleles":["CCCCC","CCCC"],"end":140488075,"clinical_significance":[],"seq_region_name":"7","id":"rs1795361214"},{"strand":1,"feature_type":"variation","end":140488072,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488072,"source":"dbSNP","seq_region_name":"7","id":"rs1356217311","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795361246","alleles":["C","A"],"end":140488075,"feature_type":"variation","strand":1,"source":"dbSNP","start":140488075,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795361266","alleles":["A","G"],"end":140488076,"feature_type":"variation","strand":1,"source":"dbSNP","start":140488076,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1795361284","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140488078,"strand":1,"feature_type":"variation","start":140488078,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs188954670","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488081,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140488081},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140488084,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488084,"source":"dbSNP","seq_region_name":"7","id":"rs1795361330","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1044246961","source":"dbSNP","start":140488085,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140488085,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795361426","feature_type":"variation","strand":1,"end":140488086,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488086},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488087,"feature_type":"variation","strand":1,"end":140488087,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795361460"},{"end":140488089,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140488089,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1460403787"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488090,"feature_type":"variation","strand":1,"end":140488090,"alleles":["T","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795361528"},{"seq_region_name":"7","id":"rs1034968901","clinical_significance":[],"start":140488093,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140488093,"alleles":["A","C","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs898957775","clinical_significance":[],"start":140488093,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AAAAAAA","AAAAAAAA"],"end":140488099,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140488094,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140488094,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs2130403194","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488100,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140488100,"clinical_significance":[],"id":"rs1795361629","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140488101,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488101,"clinical_significance":[],"seq_region_name":"7","id":"rs1795361657"},{"feature_type":"variation","strand":1,"end":140488104,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488104,"clinical_significance":[],"seq_region_name":"7","id":"rs1795361679"},{"feature_type":"variation","strand":1,"end":140488108,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488108,"clinical_significance":[],"id":"rs1330494885","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795361727","source":"dbSNP","start":140488109,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140488109,"alleles":["T","G"],"feature_type":"variation","strand":1},{"id":"rs1585514519","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488110,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140488110},{"clinical_significance":[],"id":"rs1383230990","seq_region_name":"7","source":"dbSNP","start":140488111,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140488111,"alleles":["A","G"],"feature_type":"variation","strand":1},{"start":140488112,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140488112,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs959481112","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs751602603","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488113,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140488113},{"feature_type":"variation","strand":1,"alleles":["GG","G"],"end":140488114,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488113,"clinical_significance":[],"seq_region_name":"7","id":"rs1391029987"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488116,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140488116,"clinical_significance":[],"seq_region_name":"7","id":"rs1422516594"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488117,"feature_type":"variation","strand":1,"end":140488117,"alleles":["G","T"],"clinical_significance":[],"id":"rs1795361948","seq_region_name":"7"},{"end":140488118,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140488118,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1384311574","clinical_significance":[]},{"seq_region_name":"7","id":"rs990861137","clinical_significance":[],"strand":1,"feature_type":"variation","end":140488119,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488119,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs116774569","feature_type":"variation","strand":1,"end":140488121,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488121},{"id":"rs1231077111","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488122,"source":"dbSNP","strand":1,"feature_type":"variation","end":140488122,"alleles":["G","A"]},{"start":140488133,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140488133,"alleles":["T","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795362118","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140488134,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488134,"clinical_significance":[],"seq_region_name":"7","id":"rs1317471871"},{"alleles":["CTACT","CT"],"end":140488143,"feature_type":"variation","strand":1,"source":"dbSNP","start":140488139,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1181244695","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1286633612","source":"dbSNP","start":140488140,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140488140,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488142,"feature_type":"variation","strand":1,"end":140488142,"alleles":["C","T"],"clinical_significance":[],"id":"rs952283995","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795362251","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140488145,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488145,"source":"dbSNP"},{"alleles":["C","T"],"end":140488151,"strand":1,"feature_type":"variation","start":140488151,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795362288","clinical_significance":[]},{"end":140488153,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140488153,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795362341","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795362370","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140488156,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488156},{"start":140488157,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140488157,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs1795362399","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795362416","end":140488159,"alleles":["C","A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140488159,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1585514540","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140488160,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488160,"source":"dbSNP"},{"seq_region_name":"7","id":"rs574366893","clinical_significance":[],"start":140488166,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140488166,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488167,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140488167,"clinical_significance":[],"seq_region_name":"7","id":"rs148263575"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1294263446","end":140488168,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140488168,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140488170,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488170,"clinical_significance":[],"seq_region_name":"7","id":"rs908144944"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1220453474","feature_type":"variation","strand":1,"end":140488171,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488171},{"clinical_significance":[],"seq_region_name":"7","id":"rs1359193042","end":140488173,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140488173,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140488174,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140488174,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs944964371","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140488175,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488175,"clinical_significance":[],"id":"rs1795362691","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1019340746","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488176,"feature_type":"variation","strand":1,"end":140488176,"alleles":["C","A"]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140488181,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488181,"source":"dbSNP","id":"rs1795362743","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140488182,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488182,"source":"dbSNP","seq_region_name":"7","id":"rs975781360","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795362931","clinical_significance":[],"start":140488183,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140488183,"strand":1,"feature_type":"variation"},{"id":"rs1795362958","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488184,"source":"dbSNP","strand":1,"feature_type":"variation","end":140488184,"alleles":["A","G"]},{"clinical_significance":[],"id":"rs1273798822","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488185,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140488185},{"alleles":["G","A"],"end":140488188,"strand":1,"feature_type":"variation","start":140488188,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1279435092","clinical_significance":[]},{"id":"rs1440875191","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488195,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140488195},{"seq_region_name":"7","id":"rs1345521457","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140488198,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488198,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1563103470","clinical_significance":[],"start":140488200,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140488200,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1795363063","seq_region_name":"7","source":"dbSNP","start":140488204,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140488204,"alleles":["A","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs921597137","source":"dbSNP","start":140488208,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140488208,"alleles":["C","A","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs931725623","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140488209,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488209},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488210,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140488210,"clinical_significance":[],"id":"rs1795363124","seq_region_name":"7"},{"end":140488211,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140488211,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795363141","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585514567","clinical_significance":[],"start":140488212,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140488212,"strand":1,"feature_type":"variation"},{"end":140488213,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140488213,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795363174","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488214,"source":"dbSNP","strand":1,"feature_type":"variation","end":140488214,"alleles":["T","-"],"seq_region_name":"7","id":"rs1795363195","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1257862888","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488217,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140488217},{"clinical_significance":[],"id":"rs1364570055","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["CTC","C"],"end":140488220,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488218},{"clinical_significance":[],"id":"rs553735302","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488224,"feature_type":"variation","strand":1,"end":140488224,"alleles":["C","G"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488228,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140488228,"clinical_significance":[],"seq_region_name":"7","id":"rs915415562"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1402215176","source":"dbSNP","start":140488233,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140488233,"alleles":["C","T"],"feature_type":"variation","strand":1},{"alleles":["C","G"],"end":140488235,"strand":1,"feature_type":"variation","start":140488235,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1462067521","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795363346","clinical_significance":[],"start":140488236,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140488236,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs968183954","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140488237,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488237},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140488238,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488238,"source":"dbSNP","seq_region_name":"7","id":"rs374495127","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140488239,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488239,"source":"dbSNP","seq_region_name":"7","id":"rs2130403381","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795363405","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488243,"feature_type":"variation","strand":1,"end":140488243,"alleles":["C","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488246,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140488246,"clinical_significance":[],"seq_region_name":"7","id":"rs892980972"},{"alleles":["G","A"],"end":140488247,"strand":1,"feature_type":"variation","start":140488247,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs545707291","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs76518658","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488251,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140488251},{"start":140488252,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140488252,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795363502","clinical_significance":[]},{"id":"rs112974898","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140488262,"alleles":["AAAAAAAAAAA","AAAAAAAAAA","AAAAAAAAAAAA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488252,"source":"dbSNP"},{"end":140488253,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140488253,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs76747220","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140488255,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488255,"source":"dbSNP","id":"rs1264140868","seq_region_name":"7","clinical_significance":[]},{"start":140488257,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140488257,"alleles":["A","G"],"strand":1,"feature_type":"variation","id":"rs569619617","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140488258,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488258,"source":"dbSNP","seq_region_name":"7","id":"rs182034685","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140488260,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488260,"clinical_significance":[],"seq_region_name":"7","id":"rs907141258"},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140488265,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488265,"clinical_significance":[],"seq_region_name":"7","id":"rs1795363660"},{"clinical_significance":[],"seq_region_name":"7","id":"rs565058934","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488266,"feature_type":"variation","strand":1,"alleles":["ACGTAGTGTTAAAGGAAAATAAA","A"],"end":140488288},{"end":140488267,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140488267,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs754814999"},{"seq_region_name":"7","id":"rs141371264","clinical_significance":[],"strand":1,"feature_type":"variation","end":140488268,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488268,"source":"dbSNP"},{"end":140488271,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140488271,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1044537858"},{"source":"dbSNP","start":140488273,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140488273,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs899033577","seq_region_name":"7"},{"start":140488283,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140488283,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795363812","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs543889306","end":140488284,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140488284,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140488287,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488287,"source":"dbSNP","id":"rs562087501","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140488288,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140488288,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795363871"},{"seq_region_name":"7","id":"rs1012293415","clinical_significance":[],"start":140488290,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140488290,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1432678374","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140488291,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488291},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795363925","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140488292,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488292},{"seq_region_name":"7","id":"rs1795363943","clinical_significance":[],"end":140488296,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140488296,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140488300,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140488300,"strand":1,"feature_type":"variation","id":"rs1027672261","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","A"],"end":140488301,"feature_type":"variation","strand":1,"source":"dbSNP","start":140488301,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1317574918"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488304,"feature_type":"variation","strand":1,"end":140488304,"alleles":["A","G"],"clinical_significance":[],"id":"rs1406682915","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488311,"source":"dbSNP","strand":1,"feature_type":"variation","end":140488311,"alleles":["A","G"],"id":"rs1585514653","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488312,"source":"dbSNP","strand":1,"feature_type":"variation","end":140488312,"alleles":["G","A"],"seq_region_name":"7","id":"rs752341835","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1431348172","source":"dbSNP","start":140488313,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140488313,"alleles":["C","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795364066","source":"dbSNP","start":140488314,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140488314,"feature_type":"variation","strand":1},{"start":140488315,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140488315,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1334371435","clinical_significance":[]},{"end":140488317,"alleles":["AAA","AA"],"strand":1,"feature_type":"variation","start":140488315,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1174429959","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140488320,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488320,"source":"dbSNP","seq_region_name":"7","id":"rs1795364108","clinical_significance":[]},{"seq_region_name":"7","id":"rs1424644937","clinical_significance":[],"end":140488323,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140488323,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1795364142","seq_region_name":"7","clinical_significance":[],"alleles":["A","G"],"end":140488324,"strand":1,"feature_type":"variation","start":140488324,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["G","A","T"],"end":140488325,"feature_type":"variation","strand":1,"source":"dbSNP","start":140488325,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1357708119"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1447556146","feature_type":"variation","strand":1,"alleles":["T","A"],"end":140488326,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488326},{"feature_type":"variation","strand":1,"alleles":["AAGCTGGAAA","AAGCTGGAAAAGCTGGAAA"],"end":140488337,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488328,"clinical_significance":[],"id":"rs1795364209","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1241955185","feature_type":"variation","strand":1,"end":140488330,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488330},{"seq_region_name":"7","id":"rs1795364424","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488332,"source":"dbSNP","strand":1,"feature_type":"variation","end":140488332,"alleles":["T","C"]},{"alleles":["C","T"],"end":140488338,"strand":1,"feature_type":"variation","start":140488338,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1211254933","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795364456","clinical_significance":[],"end":140488339,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140488339,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140488340,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140488340,"alleles":["T","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795364502","clinical_significance":[]},{"source":"dbSNP","start":140488341,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140488341,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795364517","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795364534","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488344,"feature_type":"variation","strand":1,"end":140488344,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs529391098","end":140488346,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140488346,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1364133752","source":"dbSNP","start":140488348,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140488348,"alleles":["C","A"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488349,"feature_type":"variation","strand":1,"end":140488349,"alleles":["C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795364585"},{"seq_region_name":"7","id":"rs1201258216","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140488353,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488353,"source":"dbSNP"},{"id":"rs1322167365","seq_region_name":"7","clinical_significance":[],"start":140488358,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140488358,"alleles":["T","-"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488362,"feature_type":"variation","strand":1,"end":140488362,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1015086394"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488366,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140488366,"seq_region_name":"7","id":"rs1008791014","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795364681","clinical_significance":[],"end":140488367,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140488367,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1795364701","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488370,"source":"dbSNP","strand":1,"feature_type":"variation","end":140488370,"alleles":["C","A"]},{"id":"rs1795364725","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140488371,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488371,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1359414169","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488374,"feature_type":"variation","strand":1,"alleles":["G","GG"],"end":140488374},{"clinical_significance":[],"seq_region_name":"7","id":"rs1756968228","alleles":["G","A"],"end":140488374,"feature_type":"variation","strand":1,"source":"dbSNP","start":140488374,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","T"],"end":140488378,"feature_type":"variation","strand":1,"source":"dbSNP","start":140488378,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs966735804","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488378,"feature_type":"variation","strand":1,"end":140488381,"alleles":["CCCC","CCC"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795364755"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488381,"source":"dbSNP","strand":1,"feature_type":"variation","end":140488381,"alleles":["C","A","G","T"],"seq_region_name":"7","id":"rs1212839719","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","-"],"end":140488382,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488382,"source":"dbSNP","seq_region_name":"7","id":"rs1749593032","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795364812","clinical_significance":[],"end":140488383,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140488383,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488385,"source":"dbSNP","strand":1,"feature_type":"variation","end":140488385,"alleles":["G","A"],"id":"rs1795364839","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488386,"source":"dbSNP","strand":1,"feature_type":"variation","end":140488386,"alleles":["G","A"],"seq_region_name":"7","id":"rs1795364860","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488393,"source":"dbSNP","strand":1,"feature_type":"variation","end":140488393,"alleles":["A","T"],"seq_region_name":"7","id":"rs1408237552","clinical_significance":[]},{"source":"dbSNP","start":140488400,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140488400,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs867949024"},{"clinical_significance":[],"id":"rs755745454","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488401,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140488401},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795364939","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140488402,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488402},{"seq_region_name":"7","id":"rs1172601100","clinical_significance":[],"start":140488403,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140488403,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1355126472","clinical_significance":[],"strand":1,"feature_type":"variation","end":140488404,"alleles":["T","TT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488404,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795364988","source":"dbSNP","start":140488405,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140488405,"alleles":["A","T"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488412,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140488412,"clinical_significance":[],"seq_region_name":"7","id":"rs1795365008"},{"end":140488417,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140488417,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs921607304"},{"start":140488421,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140488421,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1427028289","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488430,"feature_type":"variation","strand":1,"end":140488430,"alleles":["C","T"],"clinical_significance":[],"id":"rs1419033417","seq_region_name":"7"},{"seq_region_name":"7","id":"rs6950304","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488433,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140488433},{"start":140488435,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140488435,"strand":1,"feature_type":"variation","id":"rs559799257","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140488437,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140488437,"alleles":["A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795365154"},{"strand":1,"feature_type":"variation","end":140488440,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488440,"source":"dbSNP","seq_region_name":"7","id":"rs1795365177","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1261656481","feature_type":"variation","strand":1,"end":140488442,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488442},{"strand":1,"feature_type":"variation","end":140488447,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488447,"source":"dbSNP","seq_region_name":"7","id":"rs1795365218","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140488449,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488449,"source":"dbSNP","seq_region_name":"7","id":"rs114702055","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488454,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140488454,"clinical_significance":[],"seq_region_name":"7","id":"rs867333701"},{"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140488455,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488455,"clinical_significance":[],"seq_region_name":"7","id":"rs1795365282"},{"strand":1,"feature_type":"variation","end":140488458,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488458,"source":"dbSNP","seq_region_name":"7","id":"rs1585514722","clinical_significance":[]},{"id":"rs1795365326","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488461,"source":"dbSNP","strand":1,"feature_type":"variation","end":140488461,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130403622","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140488462,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488462},{"clinical_significance":[],"seq_region_name":"7","id":"rs1216043970","feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140488463,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488463},{"source":"dbSNP","start":140488464,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140488464,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1243390108"},{"seq_region_name":"7","id":"rs996314978","clinical_significance":[],"start":140488465,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140488465,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140488468,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140488468,"alleles":["A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1192245301"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488469,"feature_type":"variation","strand":1,"end":140488469,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1251444520"},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140488470,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488470,"clinical_significance":[],"seq_region_name":"7","id":"rs1206004344"},{"alleles":["A","C"],"end":140488472,"strand":1,"feature_type":"variation","start":140488472,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1305449293","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140488474,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488474,"source":"dbSNP","seq_region_name":"7","id":"rs1795365470","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs532433485","feature_type":"variation","strand":1,"end":140488475,"alleles":["T","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488475},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488480,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140488480,"seq_region_name":"7","id":"rs1022793628","clinical_significance":[]},{"start":140488483,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140488483,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs547466354","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488487,"source":"dbSNP","strand":1,"feature_type":"variation","end":140488487,"alleles":["A","C"],"seq_region_name":"7","id":"rs552129768","clinical_significance":[]},{"clinical_significance":[],"id":"rs1429910022","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140488491,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488491},{"feature_type":"variation","strand":1,"end":140488495,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488495,"clinical_significance":[],"seq_region_name":"7","id":"rs1451893289"},{"seq_region_name":"7","id":"rs1373958699","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140488496,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488496,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140488497,"alleles":["G","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488497,"clinical_significance":[],"seq_region_name":"7","id":"rs968214003"},{"alleles":["G","C"],"end":140488498,"strand":1,"feature_type":"variation","start":140488498,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795365662","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","G","T"],"end":140488504,"feature_type":"variation","strand":1,"source":"dbSNP","start":140488504,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1354189589"},{"seq_region_name":"7","id":"rs1164412495","clinical_significance":[],"start":140488507,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140488507,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140488508,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488508,"source":"dbSNP","seq_region_name":"7","id":"rs945801586","clinical_significance":[]},{"id":"rs1795365732","seq_region_name":"7","clinical_significance":[],"end":140488513,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140488513,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140488518,"alleles":["TTTTTT","TTTT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488513,"source":"dbSNP","id":"rs1426955223","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs185394400","clinical_significance":[],"strand":1,"feature_type":"variation","end":140488516,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488516,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1383709609","end":140488519,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140488519,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488522,"source":"dbSNP","strand":1,"feature_type":"variation","end":140488522,"alleles":["T","C"],"seq_region_name":"7","id":"rs1174065172","clinical_significance":[]},{"clinical_significance":[],"id":"rs1585514760","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488527,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140488527},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140488530,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488530,"clinical_significance":[],"id":"rs1795366030","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1424175244","clinical_significance":[],"start":140488531,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140488531,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488536,"feature_type":"variation","strand":1,"end":140488536,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1420276867"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1253250699","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140488537,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488537},{"seq_region_name":"7","id":"rs1300987728","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140488545,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488545,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1795366105","seq_region_name":"7","end":140488546,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140488546,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140488547,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C","G"],"end":140488547,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1479347884","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1414160557","feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140488551,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488551},{"id":"rs1795366162","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140488555,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488555,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795366176","clinical_significance":[],"alleles":["T","G"],"end":140488557,"strand":1,"feature_type":"variation","start":140488557,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1041973870","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488560,"feature_type":"variation","strand":1,"end":140488560,"alleles":["A","G"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488562,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140488562,"id":"rs1222694350","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488563,"source":"dbSNP","strand":1,"feature_type":"variation","end":140488563,"alleles":["G","A","T"],"seq_region_name":"7","id":"rs115740018","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs938602875","source":"dbSNP","start":140488565,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140488565,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1244930824","clinical_significance":[],"alleles":["A","G"],"end":140488567,"strand":1,"feature_type":"variation","start":140488567,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["T","G"],"end":140488570,"feature_type":"variation","strand":1,"source":"dbSNP","start":140488570,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1347134528"},{"seq_region_name":"7","id":"rs1795366297","clinical_significance":[],"alleles":["G","A"],"end":140488571,"strand":1,"feature_type":"variation","start":140488571,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488575,"source":"dbSNP","strand":1,"feature_type":"variation","end":140488575,"alleles":["A","T"],"seq_region_name":"7","id":"rs1055603094","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs757625088","feature_type":"variation","strand":1,"end":140488579,"alleles":["A","AA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488579},{"seq_region_name":"7","id":"rs73163266","clinical_significance":[],"alleles":["C","T"],"end":140488580,"strand":1,"feature_type":"variation","start":140488580,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488581,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140488581,"id":"rs1297585978","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs2130403785","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140488583,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488583},{"start":140488586,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140488586,"alleles":["A","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs568020699","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140488589,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488589,"clinical_significance":[],"id":"rs916964797","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1795366478","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488597,"feature_type":"variation","strand":1,"end":140488597,"alleles":["G","T"]},{"strand":1,"feature_type":"variation","end":140488602,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488602,"source":"dbSNP","seq_region_name":"7","id":"rs1795366495","clinical_significance":[]},{"id":"rs1795366511","seq_region_name":"7","clinical_significance":[],"alleles":["A","G"],"end":140488603,"strand":1,"feature_type":"variation","start":140488603,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs746443466","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140488610,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488610,"source":"dbSNP"},{"id":"rs2885921","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488619,"source":"dbSNP","strand":1,"feature_type":"variation","end":140488619,"alleles":["A","C"]},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140488621,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488621,"clinical_significance":[],"seq_region_name":"7","id":"rs1795366630"},{"alleles":["G","T"],"end":140488623,"strand":1,"feature_type":"variation","start":140488623,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795366648","clinical_significance":[]},{"source":"dbSNP","start":140488625,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140488625,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1454612274","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs979906562","alleles":["C","G","T"],"end":140488628,"feature_type":"variation","strand":1,"source":"dbSNP","start":140488628,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1366089169","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488628,"feature_type":"variation","strand":1,"end":140488629,"alleles":["CC","C"]},{"start":140488629,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140488629,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1416805347","clinical_significance":[]},{"start":140488630,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140488630,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs887894023","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488634,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140488634,"seq_region_name":"7","id":"rs1004967917","clinical_significance":[]},{"id":"rs553317643","seq_region_name":"7","clinical_significance":[],"end":140488635,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140488635,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140488636,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140488636,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs548610706","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795366800","end":140488637,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140488637,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1795366842","seq_region_name":"7","clinical_significance":[],"end":140488638,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140488638,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1266295832","clinical_significance":[],"alleles":["AT","-"],"end":140488639,"strand":1,"feature_type":"variation","start":140488638,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs886240026","source":"dbSNP","start":140488639,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140488639,"alleles":["T","A","G"],"feature_type":"variation","strand":1},{"end":140488648,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140488648,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795366873"},{"clinical_significance":[],"seq_region_name":"7","id":"rs997781870","alleles":["C","A","T"],"end":140488651,"feature_type":"variation","strand":1,"source":"dbSNP","start":140488651,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488652,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","G","T"],"end":140488652,"seq_region_name":"7","id":"rs1029222876","clinical_significance":[]},{"id":"rs570283304","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488654,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140488654},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795366990","source":"dbSNP","start":140488658,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140488658,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs941163718","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488660,"feature_type":"variation","strand":1,"end":140488660,"alleles":["G","A","C"]},{"seq_region_name":"7","id":"rs944608719","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140488661,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488661,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1284078698","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488662,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140488662},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795367064","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140488663,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488663},{"alleles":["G","A","C"],"end":140488665,"feature_type":"variation","strand":1,"source":"dbSNP","start":140488665,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs542717516","seq_region_name":"7"},{"source":"dbSNP","start":140488666,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140488666,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs539327826","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795367147","clinical_significance":[],"start":140488669,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140488669,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488672,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140488672,"clinical_significance":[],"seq_region_name":"7","id":"rs1795367168"},{"clinical_significance":[],"seq_region_name":"7","id":"rs557669677","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488674,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140488674},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563103553","source":"dbSNP","start":140488675,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140488675,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140488676,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488676,"clinical_significance":[],"seq_region_name":"7","id":"rs576181899"},{"alleles":["A","C"],"end":140488677,"feature_type":"variation","strand":1,"source":"dbSNP","start":140488677,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs989841498"},{"source":"dbSNP","start":140488678,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140488678,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs543204960"},{"seq_region_name":"7","id":"rs372151550","clinical_significance":[],"alleles":["G","A","T"],"end":140488679,"strand":1,"feature_type":"variation","start":140488679,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585514845","source":"dbSNP","start":140488683,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140488683,"alleles":["G","A"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140488684,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488684,"clinical_significance":[],"seq_region_name":"7","id":"rs1795367362"},{"end":140488690,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140488690,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130403941","clinical_significance":[]},{"seq_region_name":"7","id":"rs1470402240","clinical_significance":[],"strand":1,"feature_type":"variation","end":140488694,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488694,"source":"dbSNP"},{"source":"dbSNP","start":140488695,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140488695,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1430567233"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488696,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G","T"],"end":140488696,"id":"rs555546422","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140488697,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488697,"clinical_significance":[],"seq_region_name":"7","id":"rs574013032"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795367479","source":"dbSNP","start":140488699,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140488699,"alleles":["G","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs537466990","source":"dbSNP","start":140488700,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140488700,"alleles":["G","A","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs914233204","source":"dbSNP","start":140488706,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140488706,"alleles":["C","G","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs967571219","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488707,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140488707},{"clinical_significance":[],"id":"rs1795367572","seq_region_name":"7","alleles":["T","A"],"end":140488708,"feature_type":"variation","strand":1,"source":"dbSNP","start":140488708,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1585514859","clinical_significance":[],"strand":1,"feature_type":"variation","end":140488709,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488709,"source":"dbSNP"},{"start":140488710,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140488710,"alleles":["G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795367606","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488711,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140488711,"clinical_significance":[],"seq_region_name":"7","id":"rs541533204"},{"strand":1,"feature_type":"variation","end":140488712,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488712,"source":"dbSNP","id":"rs1795367636","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140488714,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488714,"clinical_significance":[],"seq_region_name":"7","id":"rs138258837"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795367652","feature_type":"variation","strand":1,"end":140488716,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488716},{"start":140488717,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C","T"],"end":140488717,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs928465376","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795367698","end":140488719,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140488719,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1158186856","seq_region_name":"7","clinical_significance":[],"start":140488720,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140488720,"alleles":["T","A","C"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140488723,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140488724,"alleles":["TT","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795367738"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488726,"feature_type":"variation","strand":1,"end":140488726,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs768726774"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488727,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140488727,"clinical_significance":[],"seq_region_name":"7","id":"rs1585514874"},{"seq_region_name":"7","id":"rs2130404026","clinical_significance":[],"start":140488729,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140488729,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130404032","feature_type":"variation","strand":1,"end":140488730,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488730},{"clinical_significance":[],"seq_region_name":"7","id":"rs1366250338","alleles":["G","T"],"end":140488733,"feature_type":"variation","strand":1,"source":"dbSNP","start":140488733,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["A","G"],"end":140488734,"feature_type":"variation","strand":1,"source":"dbSNP","start":140488734,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795367818","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130404041","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488736,"feature_type":"variation","strand":1,"end":140488736,"alleles":["T","A"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488738,"source":"dbSNP","strand":1,"feature_type":"variation","end":140488745,"alleles":["CCAAACCA","CCA"],"seq_region_name":"7","id":"rs781608565","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140488739,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488739,"source":"dbSNP","seq_region_name":"7","id":"rs2130404047","clinical_significance":[]},{"source":"dbSNP","start":140488741,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140488741,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130404051"},{"clinical_significance":[],"seq_region_name":"7","id":"rs960860205","alleles":["C","A"],"end":140488743,"feature_type":"variation","strand":1,"source":"dbSNP","start":140488743,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140488744,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140488744,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1293922628","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1381985740","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488745,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140488745},{"clinical_significance":[],"seq_region_name":"7","id":"rs1407348332","feature_type":"variation","strand":1,"end":140488748,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488748},{"clinical_significance":[],"seq_region_name":"7","id":"rs1322185080","source":"dbSNP","start":140488751,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140488751,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs2130404075","seq_region_name":"7","source":"dbSNP","start":140488753,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140488753,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140488755,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488755,"source":"dbSNP","seq_region_name":"7","id":"rs1055535670","clinical_significance":[]},{"alleles":["C","G"],"end":140488756,"strand":1,"feature_type":"variation","start":140488756,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795367977","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795367997","seq_region_name":"7","source":"dbSNP","start":140488757,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140488757,"feature_type":"variation","strand":1},{"start":140488758,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140488758,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs1470674750","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795368028","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488761,"feature_type":"variation","strand":1,"end":140488761,"alleles":["T","C"]},{"end":140488766,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140488766,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1403199232"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488768,"source":"dbSNP","strand":1,"feature_type":"variation","end":140488768,"alleles":["C","G","T"],"seq_region_name":"7","id":"rs1772383595","clinical_significance":[]},{"end":140488769,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140488769,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1024296600","seq_region_name":"7"},{"alleles":["T","C"],"end":140488771,"strand":1,"feature_type":"variation","start":140488771,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795368082","clinical_significance":[]},{"alleles":["A","C"],"end":140488776,"feature_type":"variation","strand":1,"source":"dbSNP","start":140488776,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795368100"},{"id":"rs1259477276","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140488778,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488778,"source":"dbSNP"},{"seq_region_name":"7","id":"rs2130404114","clinical_significance":[],"start":140488779,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140488779,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1795368128","clinical_significance":[],"start":140488783,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140488783,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs969775779","clinical_significance":[],"end":140488785,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140488785,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1374405564","seq_region_name":"7","clinical_significance":[],"start":140488786,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140488786,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140488791,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488791,"clinical_significance":[],"seq_region_name":"7","id":"rs915858497"},{"seq_region_name":"7","id":"rs1448598125","clinical_significance":[],"alleles":["A","T"],"end":140488794,"strand":1,"feature_type":"variation","start":140488794,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488797,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140488797,"seq_region_name":"7","id":"rs931224217","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs776985774","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488798,"feature_type":"variation","strand":1,"alleles":["G","A","C","T"],"end":140488798},{"seq_region_name":"7","id":"rs1185282926","clinical_significance":[],"end":140488802,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140488802,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795368296","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488803,"source":"dbSNP","strand":1,"feature_type":"variation","end":140488803,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1459914560","clinical_significance":[],"end":140488806,"alleles":["TGGT","T"],"strand":1,"feature_type":"variation","start":140488803,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488804,"source":"dbSNP","strand":1,"feature_type":"variation","end":140488804,"alleles":["G","A","T"],"id":"rs761785193","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs887747270","feature_type":"variation","strand":1,"end":140488805,"alleles":["G","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488805},{"start":140488806,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140488806,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795368378","clinical_significance":[]},{"seq_region_name":"7","id":"rs2363825","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488811,"source":"dbSNP","strand":1,"feature_type":"variation","end":140488811,"alleles":["T","C"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488813,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140488813,"clinical_significance":[],"seq_region_name":"7","id":"rs1361012812"},{"feature_type":"variation","strand":1,"end":140488818,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488818,"clinical_significance":[],"seq_region_name":"7","id":"rs1795368505"},{"clinical_significance":[],"id":"rs1795368521","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140488821,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488821},{"seq_region_name":"7","id":"rs1795368541","clinical_significance":[],"end":140488823,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140488823,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1036423033","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488828,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140488828},{"strand":1,"feature_type":"variation","end":140488833,"alleles":["T","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488833,"source":"dbSNP","seq_region_name":"7","id":"rs902033438","clinical_significance":[]},{"id":"rs774362804","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488834,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140488834},{"clinical_significance":[],"seq_region_name":"7","id":"rs1451175829","alleles":["G","T"],"end":140488836,"feature_type":"variation","strand":1,"source":"dbSNP","start":140488836,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1382695687","seq_region_name":"7","clinical_significance":[],"alleles":["G","C","T"],"end":140488838,"strand":1,"feature_type":"variation","start":140488838,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140488840,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488840,"clinical_significance":[],"seq_region_name":"7","id":"rs1289075810"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488845,"source":"dbSNP","strand":1,"feature_type":"variation","end":140488845,"alleles":["G","C"],"seq_region_name":"7","id":"rs1398213958","clinical_significance":[]},{"seq_region_name":"7","id":"rs1438255858","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140488847,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488847,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1795368762","seq_region_name":"7","feature_type":"variation","strand":1,"end":140488848,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488848},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795368829","alleles":["G","C"],"end":140488849,"feature_type":"variation","strand":1,"source":"dbSNP","start":140488849,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1428883801","end":140488851,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140488851,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795368861","end":140488851,"alleles":["G","GG"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140488851,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs983160453","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","-"],"end":140488854,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488854,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488857,"source":"dbSNP","strand":1,"feature_type":"variation","end":140488857,"alleles":["C","-"],"seq_region_name":"7","id":"rs770408194","clinical_significance":[]},{"seq_region_name":"7","id":"rs1442747170","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140488863,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488863,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1236805554","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140488865,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488865,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140488866,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488866,"source":"dbSNP","seq_region_name":"7","id":"rs1230951516","clinical_significance":[]},{"clinical_significance":[],"id":"rs1439591539","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488868,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140488868},{"start":140488870,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140488870,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs1795368992","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1585514954","seq_region_name":"7","alleles":["T","G"],"end":140488872,"feature_type":"variation","strand":1,"source":"dbSNP","start":140488872,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488877,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140488877,"seq_region_name":"7","id":"rs1795369020","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585514957","clinical_significance":[],"start":140488878,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A","C","G"],"end":140488878,"strand":1,"feature_type":"variation"},{"id":"rs1563103590","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488883,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140488883},{"clinical_significance":[],"id":"rs1795369064","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488885,"feature_type":"variation","strand":1,"end":140488885,"alleles":["G","A"]},{"source":"dbSNP","start":140488886,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140488886,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1438120018"},{"alleles":["A","G"],"end":140488890,"feature_type":"variation","strand":1,"source":"dbSNP","start":140488890,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1178226188"},{"end":140488893,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140488893,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs759562469"},{"clinical_significance":[],"id":"rs907748900","seq_region_name":"7","alleles":["T","C"],"end":140488897,"feature_type":"variation","strand":1,"source":"dbSNP","start":140488897,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140488899,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140488899,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795369179"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1360426424","feature_type":"variation","strand":1,"alleles":["A","T"],"end":140488901,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488901},{"seq_region_name":"7","id":"rs1795369213","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140488905,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488905,"source":"dbSNP"},{"source":"dbSNP","start":140488906,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140488906,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130404246"},{"clinical_significance":[],"seq_region_name":"7","id":"rs779966897","feature_type":"variation","strand":1,"alleles":["C","CC"],"end":140488907,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488907},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795369246","source":"dbSNP","start":140488909,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140488909,"alleles":["A","C"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488911,"feature_type":"variation","strand":1,"end":140488911,"alleles":["T","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795369258"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488913,"feature_type":"variation","strand":1,"end":140488913,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1244199559"},{"source":"dbSNP","start":140488915,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140488918,"alleles":["TGGG","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795369290"},{"id":"rs1356323460","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488916,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GGGGG","GGGG"],"end":140488920},{"end":140488923,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140488923,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795369328"},{"feature_type":"variation","strand":1,"end":140488924,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488924,"clinical_significance":[],"seq_region_name":"7","id":"rs1795369347"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488926,"feature_type":"variation","strand":1,"end":140488926,"alleles":["G","A"],"clinical_significance":[],"id":"rs944529645","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140488932,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488932,"source":"dbSNP","id":"rs1336955685","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs771856466","clinical_significance":[],"alleles":["CTCT","CT"],"end":140488935,"strand":1,"feature_type":"variation","start":140488932,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1935067810","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488933,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140488933},{"seq_region_name":"7","id":"rs1795369422","clinical_significance":[],"end":140488939,"alleles":["TCTGTCT","TCT"],"strand":1,"feature_type":"variation","start":140488933,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140488934,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140488934,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs545709404","clinical_significance":[]},{"end":140488935,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140488935,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795369456","clinical_significance":[]},{"id":"rs1408911545","seq_region_name":"7","clinical_significance":[],"alleles":["TGT","T"],"end":140488937,"strand":1,"feature_type":"variation","start":140488935,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1190771392","clinical_significance":[],"start":140488938,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140488938,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1029150740","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488942,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140488942},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795369538","feature_type":"variation","strand":1,"end":140488946,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488946},{"end":140488952,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140488952,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795369554","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1304778836","source":"dbSNP","start":140488954,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140488954,"alleles":["G","A","C"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140488955,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488955,"source":"dbSNP","seq_region_name":"7","id":"rs1390656541","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795369617","clinical_significance":[],"strand":1,"feature_type":"variation","end":140488956,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488956,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1411002049","clinical_significance":[],"strand":1,"feature_type":"variation","end":140488957,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488957,"source":"dbSNP"},{"start":140488958,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140488958,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs190638893","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795369682","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488960,"feature_type":"variation","strand":1,"end":140488960,"alleles":["G","A","C"]},{"seq_region_name":"7","id":"rs1362196672","clinical_significance":[],"end":140488961,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140488961,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795369715","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488966,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140488966},{"end":140488967,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140488967,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1011827499","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","G","T"],"end":140488968,"strand":1,"feature_type":"variation","start":140488968,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1490587566","clinical_significance":[]},{"seq_region_name":"7","id":"rs1021711760","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488973,"source":"dbSNP","strand":1,"feature_type":"variation","end":140488973,"alleles":["T","C"]},{"clinical_significance":[],"id":"rs1795369763","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488973,"feature_type":"variation","strand":1,"alleles":["T","-"],"end":140488973},{"start":140488974,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140488974,"strand":1,"feature_type":"variation","id":"rs531242155","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795369800","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140488975,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488975},{"seq_region_name":"7","id":"rs967035583","clinical_significance":[],"start":140488977,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140488977,"strand":1,"feature_type":"variation"},{"id":"rs796660327","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140488980,"strand":1,"feature_type":"variation","start":140488980,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795369870","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140488981,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488981,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["CTCC","C"],"end":140488990,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140488987,"source":"dbSNP","id":"rs931893095","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795369902","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140488989,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140488989},{"start":140488990,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140488990,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1044127398","clinical_significance":[]},{"alleles":["C","T"],"end":140488992,"feature_type":"variation","strand":1,"source":"dbSNP","start":140488992,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1285955472"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795369958","source":"dbSNP","start":140488993,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140488993,"alleles":["C","T"],"feature_type":"variation","strand":1},{"alleles":["T","G"],"end":140488998,"strand":1,"feature_type":"variation","start":140488998,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1227216536","clinical_significance":[]},{"source":"dbSNP","start":140488999,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140488999,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795369988","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795370008","clinical_significance":[],"start":140489002,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140489002,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs903828528","clinical_significance":[],"end":140489003,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140489003,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1384469373","seq_region_name":"7","alleles":["T","A"],"end":140489005,"feature_type":"variation","strand":1,"source":"dbSNP","start":140489005,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs146100274","clinical_significance":[],"end":140489008,"alleles":["T","A","G"],"strand":1,"feature_type":"variation","start":140489008,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140489014,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489014,"clinical_significance":[],"seq_region_name":"7","id":"rs1795370088"},{"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140489017,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489017,"clinical_significance":[],"seq_region_name":"7","id":"rs567864939"},{"end":140489018,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140489018,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs991317318"},{"source":"dbSNP","start":140489021,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140489021,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs915742612","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795370157","clinical_significance":[],"end":140489022,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140489022,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1014154023","alleles":["C","A"],"end":140489025,"feature_type":"variation","strand":1,"source":"dbSNP","start":140489025,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1340056272","seq_region_name":"7","clinical_significance":[],"start":140489026,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G","T"],"end":140489026,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1197462970","feature_type":"variation","strand":1,"alleles":["AAAAAAA","AAAAA","AAAAAA","AAAAAAAA"],"end":140489037,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489031},{"clinical_significance":[],"seq_region_name":"7","id":"rs571245949","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489033,"feature_type":"variation","strand":1,"end":140489056,"alleles":["AAAAACAAAAACAAAAACAAAAAC","AAAAACAAAAAC","AAAAACAAAAACAAAAAC","AAAAACAAAAACAAAAACAAAAACAAAAAC"]},{"feature_type":"variation","strand":1,"end":140489034,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489034,"clinical_significance":[],"seq_region_name":"7","id":"rs1795370292"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489035,"source":"dbSNP","strand":1,"feature_type":"variation","end":140489035,"alleles":["A","G"],"seq_region_name":"7","id":"rs970059099","clinical_significance":[]},{"clinical_significance":[],"id":"rs1563103624","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489038,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140489038},{"strand":1,"feature_type":"variation","alleles":["AAAAA","-"],"end":140489043,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489039,"source":"dbSNP","seq_region_name":"7","id":"rs1243122083","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["AAAAA","AAA"],"end":140489043,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489039,"clinical_significance":[],"seq_region_name":"7","id":"rs1477813364"},{"seq_region_name":"7","id":"rs1457181670","clinical_significance":[],"alleles":["A","G"],"end":140489042,"strand":1,"feature_type":"variation","start":140489042,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs995739145","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489044,"feature_type":"variation","strand":1,"end":140489044,"alleles":["C","G","T"]},{"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140489045,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489045,"clinical_significance":[],"seq_region_name":"7","id":"rs931234295"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489045,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AAAAA","AAAA"],"end":140489049,"seq_region_name":"7","id":"rs1795370686","clinical_significance":[]},{"source":"dbSNP","start":140489046,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140489046,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs984022836","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489049,"feature_type":"variation","strand":1,"end":140489049,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1323537504"},{"alleles":["AAAACTAAAA","AAAACTAAAACTAAAA"],"end":140489061,"strand":1,"feature_type":"variation","start":140489052,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1284818720","clinical_significance":[]},{"source":"dbSNP","start":140489056,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["CT","-"],"end":140489057,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795370745"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795370760","alleles":["T","A"],"end":140489057,"feature_type":"variation","strand":1,"source":"dbSNP","start":140489057,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs983232943","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489058,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140489058},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795370794","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489059,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140489059},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489065,"feature_type":"variation","strand":1,"end":140489070,"alleles":["CCTCCT","CCT"],"clinical_significance":[],"seq_region_name":"7","id":"rs1366466042"},{"clinical_significance":[],"id":"rs1185582361","seq_region_name":"7","feature_type":"variation","strand":1,"end":140489066,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489066},{"clinical_significance":[],"seq_region_name":"7","id":"rs907611422","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489067,"feature_type":"variation","strand":1,"end":140489067,"alleles":["T","G"]},{"source":"dbSNP","start":140489069,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140489069,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795370883"},{"id":"rs1795370894","seq_region_name":"7","clinical_significance":[],"start":140489071,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140489071,"alleles":["G","A","T"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140489073,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489073,"clinical_significance":[],"seq_region_name":"7","id":"rs1795370917"},{"seq_region_name":"7","id":"rs1270592387","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140489076,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489076,"source":"dbSNP"},{"start":140489079,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140489079,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs965928439","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795370960","feature_type":"variation","strand":1,"end":140489082,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489082},{"clinical_significance":[],"seq_region_name":"7","id":"rs10239030","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140489087,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489087},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140489088,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489088,"clinical_significance":[],"seq_region_name":"7","id":"rs1795371013"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1170176695","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489091,"feature_type":"variation","strand":1,"end":140489091,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1795371058","clinical_significance":[],"start":140489097,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140489097,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140489098,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489098,"source":"dbSNP","seq_region_name":"7","id":"rs1795371080","clinical_significance":[]},{"seq_region_name":"7","id":"rs940680432","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489099,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140489099},{"clinical_significance":[],"seq_region_name":"7","id":"rs1398676862","alleles":["A","G"],"end":140489100,"feature_type":"variation","strand":1,"source":"dbSNP","start":140489100,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140489102,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489102,"clinical_significance":[],"seq_region_name":"7","id":"rs1795371162"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795371185","source":"dbSNP","start":140489107,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140489107,"feature_type":"variation","strand":1},{"end":140489108,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140489108,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130404515"},{"end":140489109,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140489109,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585515116","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs538765658","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489110,"feature_type":"variation","strand":1,"end":140489110,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130404530","source":"dbSNP","start":140489113,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140489113,"alleles":["T","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1470348809","clinical_significance":[],"end":140489116,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140489116,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140489126,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489126,"source":"dbSNP","id":"rs1795371250","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs760562181","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489127,"feature_type":"variation","strand":1,"end":140489127,"alleles":["C","G"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489128,"source":"dbSNP","strand":1,"feature_type":"variation","end":140489128,"alleles":["C","T"],"id":"rs1795371289","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795371312","clinical_significance":[],"start":140489131,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140489131,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489132,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140489132,"clinical_significance":[],"seq_region_name":"7","id":"rs547120314"},{"start":140489133,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140489133,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs901955102","clinical_significance":[]},{"start":140489134,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140489134,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795371368","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140489136,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489136,"clinical_significance":[],"seq_region_name":"7","id":"rs1337726162"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489137,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140489137,"seq_region_name":"7","id":"rs1420461937","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140489138,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489138,"source":"dbSNP","seq_region_name":"7","id":"rs933382005","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489139,"source":"dbSNP","strand":1,"feature_type":"variation","end":140489139,"alleles":["A","T"],"seq_region_name":"7","id":"rs1050621506","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795371484","clinical_significance":[],"strand":1,"feature_type":"variation","end":140489140,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489140,"source":"dbSNP"},{"clinical_significance":[],"id":"rs763636689","seq_region_name":"7","source":"dbSNP","start":140489144,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140489144,"alleles":["C","G","T"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140489147,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489147,"clinical_significance":[],"seq_region_name":"7","id":"rs1795371526"},{"feature_type":"variation","strand":1,"end":140489152,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489152,"clinical_significance":[],"seq_region_name":"7","id":"rs1795371544"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489153,"feature_type":"variation","strand":1,"end":140489153,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795371560"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795371577","end":140489155,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140489155,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140489157,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489157,"clinical_significance":[],"seq_region_name":"7","id":"rs1795371589"},{"seq_region_name":"7","id":"rs1326474566","clinical_significance":[],"strand":1,"feature_type":"variation","end":140489159,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489159,"source":"dbSNP"},{"alleles":["A","G"],"end":140489161,"strand":1,"feature_type":"variation","start":140489161,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs71213485","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1021848883","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489162,"feature_type":"variation","strand":1,"end":140489162,"alleles":["T","A","C"]},{"end":140489164,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140489164,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1317167678","clinical_significance":[]},{"start":140489165,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140489165,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1223903608","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795371720","feature_type":"variation","strand":1,"alleles":["TTT","TT"],"end":140489169,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489167},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489169,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140489169,"seq_region_name":"7","id":"rs1795371738","clinical_significance":[]},{"start":140489170,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140489170,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs902865293","clinical_significance":[]},{"source":"dbSNP","start":140489176,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140489180,"alleles":["AGGAG","AG"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1264768290","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140489182,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489182,"clinical_significance":[],"seq_region_name":"7","id":"rs1484386721"},{"id":"rs1795371823","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140489183,"strand":1,"feature_type":"variation","start":140489183,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489186,"feature_type":"variation","strand":1,"end":140489186,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585515152"},{"id":"rs998560930","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489191,"source":"dbSNP","strand":1,"feature_type":"variation","end":140489191,"alleles":["T","A","G"]},{"clinical_significance":[],"id":"rs1795371871","seq_region_name":"7","feature_type":"variation","strand":1,"end":140489195,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489195},{"start":140489197,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140489197,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795371888","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140489201,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489201,"source":"dbSNP","seq_region_name":"7","id":"rs1035311816","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140489210,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489210,"source":"dbSNP","id":"rs1795371921","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140489211,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489211,"source":"dbSNP","seq_region_name":"7","id":"rs547689179","clinical_significance":[]},{"source":"dbSNP","start":140489212,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140489212,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1013642931"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489216,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140489216,"clinical_significance":[],"seq_region_name":"7","id":"rs1795371989"},{"alleles":["G","T"],"end":140489222,"strand":1,"feature_type":"variation","start":140489222,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1384863207","clinical_significance":[]},{"end":140489224,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","start":140489224,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1301215818","clinical_significance":[]},{"seq_region_name":"7","id":"rs1045649365","clinical_significance":[],"alleles":["C","A","T"],"end":140489227,"strand":1,"feature_type":"variation","start":140489227,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs959821732","seq_region_name":"7","alleles":["G","A"],"end":140489228,"feature_type":"variation","strand":1,"source":"dbSNP","start":140489228,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1355370148","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489228,"feature_type":"variation","strand":1,"alleles":["G","-"],"end":140489228},{"seq_region_name":"7","id":"rs1795372109","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140489229,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489229,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1447674225","end":140489229,"alleles":["-","TTT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140489230,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489236,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140489236,"seq_region_name":"7","id":"rs991160561","clinical_significance":[]},{"seq_region_name":"7","id":"rs1563103662","clinical_significance":[],"strand":1,"feature_type":"variation","end":140489239,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489239,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489240,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140489240,"clinical_significance":[],"id":"rs1795372184","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795372204","source":"dbSNP","start":140489240,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140489256,"alleles":["AATGTTGCCTGTAATCA","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs756758438","clinical_significance":[],"start":140489245,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140489245,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489246,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140489246,"seq_region_name":"7","id":"rs113412344","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs539092603","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489249,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140489249},{"seq_region_name":"7","id":"rs762517267","clinical_significance":[],"start":140489251,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TAATCACATAGCCCATAA","TAA"],"end":140489268,"strand":1,"feature_type":"variation"},{"id":"rs984465356","seq_region_name":"7","clinical_significance":[],"alleles":["T","A"],"end":140489254,"strand":1,"feature_type":"variation","start":140489254,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795372343","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489256,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140489256},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140489257,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489257,"source":"dbSNP","id":"rs908482162","seq_region_name":"7","clinical_significance":[]},{"end":140489259,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140489259,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs939916832","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1014574787","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489261,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140489261},{"id":"rs1206115261","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489266,"source":"dbSNP","strand":1,"feature_type":"variation","end":140489266,"alleles":["T","G"]},{"alleles":["G","A"],"end":140489269,"feature_type":"variation","strand":1,"source":"dbSNP","start":140489269,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs972121963","seq_region_name":"7"},{"start":140489270,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A","C"],"end":140489270,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1273695843","clinical_significance":[]},{"seq_region_name":"7","id":"rs1246406130","clinical_significance":[],"start":140489272,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140489272,"alleles":["A","AA"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489273,"feature_type":"variation","strand":1,"end":140489273,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795372505"},{"source":"dbSNP","start":140489279,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140489279,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795372536","seq_region_name":"7"},{"source":"dbSNP","start":140489282,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140489282,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1563103677"},{"alleles":["G","C"],"end":140489284,"feature_type":"variation","strand":1,"source":"dbSNP","start":140489284,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795372571","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs923262076","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489286,"feature_type":"variation","strand":1,"end":140489286,"alleles":["G","A"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489297,"feature_type":"variation","strand":1,"end":140489297,"alleles":["T","C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs750878311"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795372628","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140489301,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489301},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140489302,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489302,"clinical_significance":[],"seq_region_name":"7","id":"rs975821805"},{"start":140489308,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140489308,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs557332544","clinical_significance":[]},{"seq_region_name":"7","id":"rs1374075625","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489320,"source":"dbSNP","strand":1,"feature_type":"variation","end":140489320,"alleles":["C","A","T"]},{"seq_region_name":"7","id":"rs1795372708","clinical_significance":[],"start":140489322,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140489322,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795372725","source":"dbSNP","start":140489323,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140489323,"feature_type":"variation","strand":1},{"id":"rs1050465145","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140489325,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489325,"source":"dbSNP"},{"source":"dbSNP","start":140489327,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140489327,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795372752"},{"source":"dbSNP","start":140489328,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140489329,"alleles":["GG","GGG"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795372766","seq_region_name":"7"},{"source":"dbSNP","start":140489332,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140489332,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1408304317"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489334,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140489334,"seq_region_name":"7","id":"rs2130404749","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489336,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140489336,"clinical_significance":[],"seq_region_name":"7","id":"rs180836291"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140489337,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489337,"source":"dbSNP","seq_region_name":"7","id":"rs1795372827","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489339,"source":"dbSNP","strand":1,"feature_type":"variation","end":140489339,"alleles":["C","T"],"seq_region_name":"7","id":"rs889299843","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585515195","source":"dbSNP","start":140489346,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140489346,"feature_type":"variation","strand":1},{"id":"rs947555732","seq_region_name":"7","clinical_significance":[],"alleles":["G","T"],"end":140489350,"strand":1,"feature_type":"variation","start":140489350,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["G","C"],"end":140489351,"feature_type":"variation","strand":1,"source":"dbSNP","start":140489351,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795372895"},{"alleles":["A","T"],"end":140489352,"strand":1,"feature_type":"variation","start":140489352,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1043604526","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140489354,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489354,"source":"dbSNP","seq_region_name":"7","id":"rs1385170260","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489357,"feature_type":"variation","strand":1,"end":140489357,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs903469602"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563103685","source":"dbSNP","start":140489365,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140489365,"alleles":["A","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs979348731","seq_region_name":"7","alleles":["A","G"],"end":140489366,"feature_type":"variation","strand":1,"source":"dbSNP","start":140489366,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140489367,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G","T"],"end":140489367,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795373005"},{"seq_region_name":"7","id":"rs2130404794","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489369,"source":"dbSNP","strand":1,"feature_type":"variation","end":140489369,"alleles":["A","G"]},{"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140489375,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489375,"source":"dbSNP","id":"rs1795373019","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs4257939","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489376,"feature_type":"variation","strand":1,"end":140489376,"alleles":["T","A","C"]},{"id":"rs1164615461","seq_region_name":"7","clinical_significance":[],"start":140489376,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TA","-"],"end":140489377,"strand":1,"feature_type":"variation"},{"end":140489378,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140489378,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1295739304"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795373149","feature_type":"variation","strand":1,"end":140489382,"alleles":["CGGCC","CGGCCGGGCGGCC"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489378},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795373178","feature_type":"variation","strand":1,"end":140489379,"alleles":["G","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489379},{"start":140489380,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140489380,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1183671906","clinical_significance":[]},{"end":140489381,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140489381,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1481895209","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1050807978","alleles":["C","A","G","T"],"end":140489382,"feature_type":"variation","strand":1,"source":"dbSNP","start":140489382,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs10235810","seq_region_name":"7","clinical_significance":[],"start":140489383,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140489383,"alleles":["A","G","T"],"strand":1,"feature_type":"variation"},{"start":140489386,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140489386,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1285000116","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs185244236","source":"dbSNP","start":140489387,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140489387,"alleles":["G","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1563103701","clinical_significance":[],"alleles":["-","GC"],"end":140489387,"strand":1,"feature_type":"variation","start":140489388,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1052400312","source":"dbSNP","start":140489388,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140489388,"alleles":["C","A","T"],"feature_type":"variation","strand":1},{"id":"rs10277322","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489389,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140489389},{"seq_region_name":"7","id":"rs1563103708","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489390,"source":"dbSNP","strand":1,"feature_type":"variation","end":140489390,"alleles":["G","GGCGCAG"]},{"id":"rs535103900","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489391,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140489391},{"feature_type":"variation","strand":1,"end":140489392,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489392,"clinical_significance":[],"seq_region_name":"7","id":"rs1296808563"},{"clinical_significance":[],"id":"rs373413775","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489398,"feature_type":"variation","strand":1,"end":140489398,"alleles":["C","A","T"]},{"start":140489399,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140489399,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1255641713","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1407156263","feature_type":"variation","strand":1,"alleles":["GCCTGTAATCCCAGC","GCCTGTAATCCCAGCCTGTAATCCCAGC"],"end":140489413,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489399},{"id":"rs949503915","seq_region_name":"7","clinical_significance":[],"start":140489401,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140489401,"alleles":["C","G","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs866901609","clinical_significance":[],"strand":1,"feature_type":"variation","end":140489403,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489403,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs578069276","end":140489404,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140489404,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489408,"feature_type":"variation","strand":1,"end":140489408,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585515262"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489410,"source":"dbSNP","strand":1,"feature_type":"variation","end":140489410,"alleles":["C","T"],"seq_region_name":"7","id":"rs1218971392","clinical_significance":[]},{"clinical_significance":[],"id":"rs111671465","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140489413,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489413},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795374636","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489414,"feature_type":"variation","strand":1,"end":140489414,"alleles":["A","G"]},{"clinical_significance":[],"id":"rs1585515271","seq_region_name":"7","source":"dbSNP","start":140489415,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140489415,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795374688","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["TTT","TT"],"end":140489418,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489416,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489417,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140489417,"seq_region_name":"7","id":"rs1035323221","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140489419,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489419,"source":"dbSNP","seq_region_name":"7","id":"rs1199619701","clinical_significance":[]},{"id":"rs1410771869","seq_region_name":"7","clinical_significance":[],"start":140489419,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140489421,"alleles":["GGG","GGGG"],"strand":1,"feature_type":"variation"},{"start":140489420,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140489420,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795374800","clinical_significance":[]},{"alleles":["AG","AGCCTTCTATTTTAAG"],"end":140489423,"strand":1,"feature_type":"variation","start":140489422,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1488279143","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1219839674","alleles":["-","CCTTCTATTTTAA","CCTTCTATTTTAAGGCTGAGAAATAAGGAATATCCTA"],"end":140489423,"feature_type":"variation","strand":1,"source":"dbSNP","start":140489424,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1434529326","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489424,"feature_type":"variation","strand":1,"end":140489424,"alleles":["G","C"]},{"seq_region_name":"7","id":"rs1319364553","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489425,"source":"dbSNP","strand":1,"feature_type":"variation","end":140489424,"alleles":["-","GCTGAGAAATAAGGAATAT","GCTGAGAAATAAGGAATATCCTAGCTTCTGAGGATTACTTTTTTTTTTTTTTTTAGA"]},{"start":140489425,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140489425,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1265083677","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140489425,"alleles":["-","TGAGAAATAAGGAATATCCTAGCTT","TGAGAAATAAGGAATATCCTAGCTTCTGAGGATTACTTTTT","TT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489426,"clinical_significance":[],"seq_region_name":"7","id":"rs1585515291"},{"seq_region_name":"7","id":"rs1200745450","clinical_significance":[],"start":140489426,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140489426,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"id":"rs1270045633","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489427,"source":"dbSNP","strand":1,"feature_type":"variation","end":140489427,"alleles":["A","G","T"]},{"strand":1,"feature_type":"variation","end":140489427,"alleles":["-","CC"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489428,"source":"dbSNP","seq_region_name":"7","id":"rs2130404953","clinical_significance":[]},{"alleles":["C","A","T"],"end":140489431,"feature_type":"variation","strand":1,"source":"dbSNP","start":140489431,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1431825109"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1262370784","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140489432,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489432},{"clinical_significance":[],"id":"rs1206941268","seq_region_name":"7","end":140489435,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140489435,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs545376562","feature_type":"variation","strand":1,"end":140489436,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489436},{"end":140489437,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140489437,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs563684553"},{"end":140489442,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140489442,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1364028645"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489443,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140489443,"seq_region_name":"7","id":"rs575816385","clinical_significance":[]},{"source":"dbSNP","start":140489447,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140489447,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs190054399"},{"seq_region_name":"7","id":"rs561301996","clinical_significance":[],"alleles":["T","C"],"end":140489448,"strand":1,"feature_type":"variation","start":140489448,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1364731598","clinical_significance":[],"start":140489449,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140489449,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"id":"rs528719728","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489451,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140489451},{"end":140489452,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140489452,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs547081759","clinical_significance":[]},{"end":140489453,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140489453,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs181295876","clinical_significance":[]},{"source":"dbSNP","start":140489454,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140489454,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795375531"},{"id":"rs532873079","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489455,"source":"dbSNP","strand":1,"feature_type":"variation","end":140489455,"alleles":["T","G"]},{"seq_region_name":"7","id":"rs543466390","clinical_significance":[],"alleles":["C","A","G","T"],"end":140489456,"strand":1,"feature_type":"variation","start":140489456,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489457,"feature_type":"variation","strand":1,"end":140489457,"alleles":["G","A","C"],"clinical_significance":[],"id":"rs1386012963","seq_region_name":"7"},{"source":"dbSNP","start":140489461,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140489461,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs983998268"},{"start":140489464,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C","G"],"end":140489464,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795375705","clinical_significance":[]},{"seq_region_name":"7","id":"rs1428852965","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489465,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140489465},{"alleles":["T","C"],"end":140489467,"strand":1,"feature_type":"variation","start":140489467,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1249823005","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489470,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140489470,"seq_region_name":"7","id":"rs1186535654","clinical_significance":[]},{"id":"rs536922933","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140489471,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489471,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795375786","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489472,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140489472},{"seq_region_name":"7","id":"rs1336634791","clinical_significance":[],"start":140489475,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140489475,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1202219916","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489476,"feature_type":"variation","strand":1,"end":140489476,"alleles":["C","T"]},{"end":140489477,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140489477,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs529865595","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795375861","clinical_significance":[],"end":140489479,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140489479,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["C","T"],"end":140489486,"strand":1,"feature_type":"variation","start":140489486,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1255585243","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140489488,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489488,"source":"dbSNP","seq_region_name":"7","id":"rs144798729","clinical_significance":[]},{"id":"rs1795375921","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140489489,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489489,"source":"dbSNP"},{"clinical_significance":[],"id":"rs2130405057","seq_region_name":"7","alleles":["C","G"],"end":140489490,"feature_type":"variation","strand":1,"source":"dbSNP","start":140489490,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1284025459","clinical_significance":[],"alleles":["AAAAA","AAAA","AAAAAA"],"end":140489501,"strand":1,"feature_type":"variation","start":140489497,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs148574521","feature_type":"variation","strand":1,"end":140489499,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489499},{"alleles":["A","C"],"end":140489500,"feature_type":"variation","strand":1,"source":"dbSNP","start":140489500,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1384140744"},{"seq_region_name":"7","id":"rs576825170","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140489505,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489505,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795376016","clinical_significance":[],"start":140489516,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140489516,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs199766788","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489520,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140489520},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489523,"source":"dbSNP","strand":1,"feature_type":"variation","end":140489523,"alleles":["G","A"],"seq_region_name":"7","id":"rs1399655398","clinical_significance":[]},{"seq_region_name":"7","id":"rs200444479","clinical_significance":[],"end":140489524,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","start":140489524,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1171565215","seq_region_name":"7","source":"dbSNP","start":140489524,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TGTGGTGGTGGGGGCCTGT","TGT"],"end":140489542,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1166482173","clinical_significance":[],"end":140489525,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140489525,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1795376155","seq_region_name":"7","clinical_significance":[],"start":140489527,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140489527,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1448836523","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489531,"source":"dbSNP","strand":1,"feature_type":"variation","end":140489531,"alleles":["G","A"]},{"strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140489532,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489532,"source":"dbSNP","seq_region_name":"7","id":"rs751196807","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489533,"feature_type":"variation","strand":1,"end":140489537,"alleles":["GGGGG","GGGG"],"clinical_significance":[],"id":"rs1795376211","seq_region_name":"7"},{"alleles":["G","A"],"end":140489534,"strand":1,"feature_type":"variation","start":140489534,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1440701027","clinical_significance":[]},{"seq_region_name":"7","id":"rs1251676367","clinical_significance":[],"strand":1,"feature_type":"variation","end":140489536,"alleles":["G","C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489536,"source":"dbSNP"},{"alleles":["GG","CA"],"end":140489537,"strand":1,"feature_type":"variation","start":140489536,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs386718469","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140489537,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489537,"clinical_significance":[],"seq_region_name":"7","id":"rs1484156708"},{"id":"rs1795376319","seq_region_name":"7","clinical_significance":[],"start":140489538,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140489538,"alleles":["C","A","G"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489540,"source":"dbSNP","strand":1,"feature_type":"variation","end":140489540,"alleles":["T","C"],"id":"rs1795376341","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1441203197","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489544,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140489544},{"seq_region_name":"7","id":"rs541171275","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489548,"source":"dbSNP","strand":1,"feature_type":"variation","end":140489548,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795376401","alleles":["G","C"],"end":140489550,"feature_type":"variation","strand":1,"source":"dbSNP","start":140489550,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140489553,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489553,"source":"dbSNP","id":"rs1228095947","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1563103760","clinical_significance":[],"alleles":["A","G"],"end":140489559,"strand":1,"feature_type":"variation","start":140489559,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140489560,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["-","G"],"end":140489559,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795376471","clinical_significance":[]},{"alleles":["A","C","G"],"end":140489560,"feature_type":"variation","strand":1,"source":"dbSNP","start":140489560,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs905392975"},{"seq_region_name":"7","id":"rs1246357329","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140489563,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489563,"source":"dbSNP"},{"start":140489569,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140489569,"strand":1,"feature_type":"variation","id":"rs1424756945","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140489570,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489570,"source":"dbSNP","seq_region_name":"7","id":"rs1166203024","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795376656","clinical_significance":[],"start":140489577,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140489577,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1391687795","clinical_significance":[],"alleles":["G","A"],"end":140489579,"strand":1,"feature_type":"variation","start":140489579,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1348122323","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140489581,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489581,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1306012258","source":"dbSNP","start":140489585,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140489585,"alleles":["A","G"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140489589,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489589,"clinical_significance":[],"seq_region_name":"7","id":"rs1457331056"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140489592,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489592,"clinical_significance":[],"id":"rs567693233","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1444260685","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489593,"source":"dbSNP","strand":1,"feature_type":"variation","end":140489593,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795376809","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489594,"feature_type":"variation","strand":1,"end":140489594,"alleles":["G","A"]},{"alleles":["A","G"],"end":140489596,"feature_type":"variation","strand":1,"source":"dbSNP","start":140489596,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1307377087"},{"start":140489600,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140489600,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795376845","clinical_significance":[]},{"end":140489612,"alleles":["C","A","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140489612,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs578116769"},{"source":"dbSNP","start":140489613,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140489613,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1246815923"},{"id":"rs1368037928","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489615,"source":"dbSNP","strand":1,"feature_type":"variation","end":140489615,"alleles":["G","A"]},{"id":"rs1182580364","seq_region_name":"7","clinical_significance":[],"start":140489618,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","G"],"end":140489618,"strand":1,"feature_type":"variation"},{"start":140489619,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C","T"],"end":140489619,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs10952693","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs557045601","end":140489620,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140489620,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140489621,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140489621,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","id":"rs530234233","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489622,"feature_type":"variation","strand":1,"end":140489622,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs575623935"},{"seq_region_name":"7","id":"rs1585515431","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140489629,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489629,"source":"dbSNP"},{"id":"rs1795377100","seq_region_name":"7","clinical_significance":[],"end":140489630,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140489630,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs548735855","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489641,"source":"dbSNP","strand":1,"feature_type":"variation","end":140489641,"alleles":["A","G"]},{"source":"dbSNP","start":140489642,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140489642,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs561667286"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489642,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","-"],"end":140489642,"seq_region_name":"7","id":"rs1795377169","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140489643,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489643,"clinical_significance":[],"seq_region_name":"7","id":"rs563844377"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489647,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140489647,"seq_region_name":"7","id":"rs531271069","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1228452128","alleles":["A","G"],"end":140489651,"feature_type":"variation","strand":1,"source":"dbSNP","start":140489651,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795377261","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489660,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140489660},{"seq_region_name":"7","id":"rs1351979034","clinical_significance":[],"end":140489663,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140489663,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140489670,"alleles":["AAAAAAA","AAAAAAAA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489664,"clinical_significance":[],"seq_region_name":"7","id":"rs1285994612"},{"seq_region_name":"7","id":"rs1795377323","clinical_significance":[],"alleles":["-","G"],"end":140489665,"strand":1,"feature_type":"variation","start":140489666,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795377347","clinical_significance":[],"end":140489669,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140489669,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs199553818","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489670,"feature_type":"variation","strand":1,"end":140489670,"alleles":["A","T"]},{"seq_region_name":"7","id":"rs1795377388","clinical_significance":[],"end":140489670,"alleles":["-","AT"],"strand":1,"feature_type":"variation","start":140489671,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489671,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140489671,"seq_region_name":"7","id":"rs200726223","clinical_significance":[]},{"seq_region_name":"7","id":"rs1159240497","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489672,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140489672},{"seq_region_name":"7","id":"rs66481122","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489672,"source":"dbSNP","strand":1,"feature_type":"variation","end":140489681,"alleles":["AAAAAAAAAA","AAAAAAAAA","AAAAAAAAAAA","AAAAAAAAAAAA"]},{"strand":1,"feature_type":"variation","alleles":["-","T"],"end":140489672,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489673,"source":"dbSNP","id":"rs1444860094","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1410042769","alleles":["A","T"],"end":140489673,"feature_type":"variation","strand":1,"source":"dbSNP","start":140489673,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1183155853","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489674,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["-","T"],"end":140489673},{"start":140489676,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140489675,"alleles":["-","T"],"strand":1,"feature_type":"variation","id":"rs1795377578","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140489682,"alleles":["G","GG"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489682,"clinical_significance":[],"seq_region_name":"7","id":"rs1181658557"},{"seq_region_name":"7","id":"rs1795377601","clinical_significance":[],"start":140489682,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140489682,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"end":140489692,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140489692,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs571309727"},{"start":140489701,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140489701,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585515463","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs986233004","source":"dbSNP","start":140489708,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140489708,"alleles":["A","G"],"feature_type":"variation","strand":1},{"end":140489716,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140489716,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795377738","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140489728,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489728,"clinical_significance":[],"seq_region_name":"7","id":"rs910663766"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1197166757","source":"dbSNP","start":140489738,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140489738,"alleles":["A","T"],"feature_type":"variation","strand":1},{"start":140489739,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140489739,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1423212926","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1451589683","alleles":["A","G"],"end":140489751,"feature_type":"variation","strand":1,"source":"dbSNP","start":140489751,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["T","C"],"end":140489755,"strand":1,"feature_type":"variation","start":140489755,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs75106010","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1043269641","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140489756,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489756},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130405323","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489763,"feature_type":"variation","strand":1,"end":140489763,"alleles":["C","T"]},{"feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140489766,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489766,"clinical_significance":[],"seq_region_name":"7","id":"rs11764660"},{"id":"rs1795378068","seq_region_name":"7","clinical_significance":[],"end":140489769,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140489769,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140489781,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140489781,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1265679146","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140489791,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489791,"clinical_significance":[],"seq_region_name":"7","id":"rs1227470941"},{"clinical_significance":[],"seq_region_name":"7","id":"rs934937382","source":"dbSNP","start":140489793,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140489793,"alleles":["T","C"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489795,"feature_type":"variation","strand":1,"end":140489795,"alleles":["G","A"],"clinical_significance":[],"id":"rs532834700","seq_region_name":"7"},{"id":"rs1795378152","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489801,"source":"dbSNP","strand":1,"feature_type":"variation","end":140489801,"alleles":["A","C"]},{"alleles":["T","A","C"],"end":140489803,"feature_type":"variation","strand":1,"source":"dbSNP","start":140489803,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1276446031","seq_region_name":"7"},{"start":140489813,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140489813,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795378203","clinical_significance":[]},{"end":140489815,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140489815,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795378220","seq_region_name":"7"},{"id":"rs1433968572","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489820,"source":"dbSNP","strand":1,"feature_type":"variation","end":140489820,"alleles":["G","A","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489824,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140489824,"clinical_significance":[],"id":"rs1795378259","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489825,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140489825,"id":"rs1330482033","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140489832,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489832,"clinical_significance":[],"seq_region_name":"7","id":"rs1458898341"},{"seq_region_name":"7","id":"rs1795378329","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489833,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140489833},{"source":"dbSNP","start":140489840,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140489840,"alleles":["T","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs551086427"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140489860,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489860,"source":"dbSNP","seq_region_name":"7","id":"rs1795378379","clinical_significance":[]},{"alleles":["T","C"],"end":140489863,"feature_type":"variation","strand":1,"source":"dbSNP","start":140489863,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1330352727"},{"start":140489871,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140489871,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795378413","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795378437","source":"dbSNP","start":140489874,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140489874,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140489878,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140489878,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1158516274"},{"alleles":["A","G"],"end":140489879,"feature_type":"variation","strand":1,"source":"dbSNP","start":140489879,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1057288419"},{"seq_region_name":"7","id":"rs1427506736","clinical_significance":[],"start":140489883,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140489883,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1171216404","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140489901,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489901,"source":"dbSNP"},{"alleles":["G","T"],"end":140489908,"feature_type":"variation","strand":1,"source":"dbSNP","start":140489908,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1449018054"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489917,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140489917,"seq_region_name":"7","id":"rs1477864616","clinical_significance":[]},{"seq_region_name":"7","id":"rs750217280","clinical_significance":[],"start":140489923,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140489923,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140489927,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489927,"source":"dbSNP","id":"rs1243209050","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140489930,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489930,"source":"dbSNP","seq_region_name":"7","id":"rs1304715893","clinical_significance":[]},{"seq_region_name":"7","id":"rs1377106648","clinical_significance":[],"start":140489940,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140489940,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1795378648","clinical_significance":[],"start":140489941,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140489941,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"start":140489943,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140489943,"strand":1,"feature_type":"variation","id":"rs112384450","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140489949,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489949,"source":"dbSNP","seq_region_name":"7","id":"rs1296931795","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140489951,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489951,"clinical_significance":[],"seq_region_name":"7","id":"rs1795378728"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489952,"feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140489952,"clinical_significance":[],"id":"rs1207526759","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1795378759","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140489954,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489954},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795378784","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489964,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140489964},{"id":"rs1795378809","seq_region_name":"7","clinical_significance":[],"end":140489976,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140489976,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489977,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140489977,"clinical_significance":[],"seq_region_name":"7","id":"rs1795378831"},{"seq_region_name":"7","id":"rs1795378851","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140489979,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140489979},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140489980,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489980,"clinical_significance":[],"seq_region_name":"7","id":"rs1795378881"},{"start":140489984,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140489984,"alleles":["A","G"],"strand":1,"feature_type":"variation","id":"rs1312432767","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","C","T"],"end":140489986,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140489986,"clinical_significance":[],"id":"rs1795378931","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795378988","source":"dbSNP","start":140489998,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140489998,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490004,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140490004,"clinical_significance":[],"seq_region_name":"7","id":"rs1280249952"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490008,"source":"dbSNP","strand":1,"feature_type":"variation","end":140490008,"alleles":["G","A"],"seq_region_name":"7","id":"rs1795379026","clinical_significance":[]},{"end":140490009,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140490009,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795379043","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795379061","alleles":["A","G"],"end":140490010,"feature_type":"variation","strand":1,"source":"dbSNP","start":140490010,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795379079","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490013,"feature_type":"variation","strand":1,"end":140490013,"alleles":["C","A"]},{"alleles":["A","G"],"end":140490016,"strand":1,"feature_type":"variation","start":140490016,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130405457","clinical_significance":[]},{"alleles":["T","C"],"end":140490017,"feature_type":"variation","strand":1,"source":"dbSNP","start":140490017,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795379101"},{"seq_region_name":"7","id":"rs1217269770","clinical_significance":[],"start":140490033,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["GG","G"],"end":140490034,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490036,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140490036,"clinical_significance":[],"id":"rs1012561952","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1795379158","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140490041,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490041},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490048,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140490048,"seq_region_name":"7","id":"rs756102969","clinical_significance":[]},{"id":"rs1298047029","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490059,"source":"dbSNP","strand":1,"feature_type":"variation","end":140490059,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1044029374","feature_type":"variation","strand":1,"end":140490060,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490060},{"feature_type":"variation","strand":1,"alleles":["-","GTATT"],"end":140490060,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490061,"clinical_significance":[],"seq_region_name":"7","id":"rs1795379238"},{"seq_region_name":"7","id":"rs1448793686","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490061,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140490061},{"seq_region_name":"7","id":"rs1554453144","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","TATT"],"end":140490061,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490061,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490061,"feature_type":"variation","strand":1,"alleles":["TT","T"],"end":140490062,"clinical_significance":[],"seq_region_name":"7","id":"rs558684224"},{"clinical_significance":[],"seq_region_name":"7","id":"rs572248150","feature_type":"variation","strand":1,"alleles":["TTATTTTATTTTATTTT","TTATTTTATTTT","TTATTTTATTTTATTTTATTTT"],"end":140490077,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490061},{"clinical_significance":[],"seq_region_name":"7","id":"rs1361151265","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490062,"feature_type":"variation","strand":1,"end":140490062,"alleles":["T","C"]},{"source":"dbSNP","start":140490070,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140490070,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795379359"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1174146194","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140490080,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490080},{"clinical_significance":[],"seq_region_name":"7","id":"rs565719836","feature_type":"variation","strand":1,"end":140490082,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490082},{"end":140490086,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140490086,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs530565377","clinical_significance":[]},{"start":140490088,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C","G"],"end":140490088,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs536077598","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490091,"feature_type":"variation","strand":1,"end":140490113,"alleles":["TTTATTTTATTTTATTTTATTTT","TTTATTTTATTTT","TTTATTTTATTTTATTTT","TTTATTTTATTTTATTTTATTTTATTTT","TTTATTTTATTTTATTTTATTTTATTTTATTTT"],"clinical_significance":[],"seq_region_name":"7","id":"rs1170836393"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795379516","source":"dbSNP","start":140490094,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140490094,"alleles":["A","G"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140490099,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490099,"clinical_significance":[],"seq_region_name":"7","id":"rs113280040"},{"end":140490119,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140490119,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795379533","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs370755124","end":140490125,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140490125,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140490127,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","T"],"end":140490127,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1238856506","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140490128,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490128,"source":"dbSNP","id":"rs779946998","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140490133,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140490133,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs2130405537","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140490139,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490139,"clinical_significance":[],"seq_region_name":"7","id":"rs1795379616"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490146,"source":"dbSNP","strand":1,"feature_type":"variation","end":140490146,"alleles":["G","C"],"seq_region_name":"7","id":"rs1207657640","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1482657386","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490148,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140490148},{"start":140490149,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140490149,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs546784935","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs28655858","end":140490151,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140490151,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140490154,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490154,"source":"dbSNP","seq_region_name":"7","id":"rs1425696518","clinical_significance":[]},{"source":"dbSNP","start":140490156,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140490156,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1296735504"},{"seq_region_name":"7","id":"rs1476799903","clinical_significance":[],"start":140490157,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140490157,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs539113680","alleles":["A","G"],"end":140490158,"feature_type":"variation","strand":1,"source":"dbSNP","start":140490158,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs557464460","end":140490159,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140490159,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["T","C"],"end":140490162,"feature_type":"variation","strand":1,"source":"dbSNP","start":140490162,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1447622596","seq_region_name":"7"},{"id":"rs1415300351","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490163,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CTAGGCT","CT"],"end":140490169},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140490165,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490165,"source":"dbSNP","seq_region_name":"7","id":"rs1178530009","clinical_significance":[]},{"end":140490166,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140490166,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1357580246","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1447392188","source":"dbSNP","start":140490170,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140490170,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140490172,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140490172,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1298875261"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490174,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140490174,"clinical_significance":[],"seq_region_name":"7","id":"rs1342996931"},{"strand":1,"feature_type":"variation","end":140490178,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490178,"source":"dbSNP","id":"rs1398668630","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","T"],"end":140490187,"strand":1,"feature_type":"variation","start":140490187,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795379989","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140490189,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490189,"clinical_significance":[],"seq_region_name":"7","id":"rs1278007664"},{"strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140490190,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490190,"source":"dbSNP","seq_region_name":"7","id":"rs28620562","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs113086845","source":"dbSNP","start":140490191,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140490191,"alleles":["G","A","C"],"feature_type":"variation","strand":1},{"start":140490196,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140490196,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1166034923","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490197,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140490197,"clinical_significance":[],"seq_region_name":"7","id":"rs1221246064"},{"clinical_significance":[],"id":"rs1415418764","seq_region_name":"7","alleles":["G","A"],"end":140490198,"feature_type":"variation","strand":1,"source":"dbSNP","start":140490198,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1276081718","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140490200,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490200},{"clinical_significance":[],"seq_region_name":"7","id":"rs1179578620","end":140490202,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140490202,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140490204,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490204,"source":"dbSNP","id":"rs2130405646","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140490205,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490205,"source":"dbSNP","id":"rs1585515606","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140490209,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490209,"clinical_significance":[],"seq_region_name":"7","id":"rs1795380205"},{"seq_region_name":"7","id":"rs1311183986","clinical_significance":[],"start":140490221,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140490221,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs112383913","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490224,"source":"dbSNP","strand":1,"feature_type":"variation","end":140490224,"alleles":["C","A","G"]},{"feature_type":"variation","strand":1,"end":140490225,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490225,"clinical_significance":[],"id":"rs1252028416","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140490229,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490229,"source":"dbSNP","seq_region_name":"7","id":"rs1795380299","clinical_significance":[]},{"seq_region_name":"7","id":"rs1487298661","clinical_significance":[],"start":140490234,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140490234,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1207078570","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490235,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140490235},{"id":"rs1795380342","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140490238,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490238,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1481914659","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490240,"source":"dbSNP","strand":1,"feature_type":"variation","end":140490242,"alleles":["GAG","G"]},{"feature_type":"variation","strand":1,"alleles":["A","C","G","T"],"end":140490241,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490241,"clinical_significance":[],"id":"rs28530673","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1323396738","clinical_significance":[],"alleles":["G","C"],"end":140490242,"strand":1,"feature_type":"variation","start":140490242,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1310724737","clinical_significance":[],"end":140490244,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140490244,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140490245,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490245,"clinical_significance":[],"seq_region_name":"7","id":"rs1763967616"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1227762479","end":140490246,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140490246,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","T"],"end":140490250,"feature_type":"variation","strand":1,"source":"dbSNP","start":140490250,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795380474"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490252,"feature_type":"variation","strand":1,"end":140490252,"alleles":["A","G"],"clinical_significance":[],"id":"rs1351368960","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1269446005","end":140490253,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140490253,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490254,"source":"dbSNP","strand":1,"feature_type":"variation","end":140490254,"alleles":["G","A"],"id":"rs1370397339","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1294485459","clinical_significance":[],"start":140490258,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140490258,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1478892368","end":140490260,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140490260,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs113104489","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490264,"source":"dbSNP","strand":1,"feature_type":"variation","end":140490264,"alleles":["T","A"]},{"seq_region_name":"7","id":"rs1459935968","clinical_significance":[],"strand":1,"feature_type":"variation","end":140490269,"alleles":["TTTTTT","TTTTT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490264,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140490283,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490283,"clinical_significance":[],"seq_region_name":"7","id":"rs1348626019"},{"seq_region_name":"7","id":"rs28524976","clinical_significance":[],"start":140490284,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C","G","T"],"end":140490284,"strand":1,"feature_type":"variation"},{"end":140490285,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140490285,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795380695","clinical_significance":[]},{"seq_region_name":"7","id":"rs1412266974","clinical_significance":[],"end":140490286,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140490286,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140490287,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490287,"source":"dbSNP","seq_region_name":"7","id":"rs1471400830","clinical_significance":[]},{"source":"dbSNP","start":140490287,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["GGGG","GGG"],"end":140490290,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1183967633"},{"clinical_significance":[],"id":"rs1585515667","seq_region_name":"7","alleles":["T","G"],"end":140490291,"feature_type":"variation","strand":1,"source":"dbSNP","start":140490291,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1249601941","seq_region_name":"7","alleles":["T","A"],"end":140490292,"feature_type":"variation","strand":1,"source":"dbSNP","start":140490292,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140490295,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140490295,"alleles":["A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795380788","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140490297,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490297,"source":"dbSNP","seq_region_name":"7","id":"rs573165714","clinical_significance":[]},{"clinical_significance":[],"id":"rs540546456","seq_region_name":"7","feature_type":"variation","strand":1,"end":140490298,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490298},{"alleles":["A","G"],"end":140490312,"strand":1,"feature_type":"variation","start":140490312,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795380846","clinical_significance":[]},{"id":"rs1220932526","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490314,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140490314},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490317,"source":"dbSNP","strand":1,"feature_type":"variation","end":140490317,"alleles":["C","G"],"seq_region_name":"7","id":"rs1329869067","clinical_significance":[]},{"end":140490318,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140490318,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795380890","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140490322,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490322,"clinical_significance":[],"seq_region_name":"7","id":"rs1795380911"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1270078987","source":"dbSNP","start":140490333,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140490333,"feature_type":"variation","strand":1},{"id":"rs1159378781","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["TCTGCCCGCCTCGTC","TC"],"end":140490350,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490336,"source":"dbSNP"},{"id":"rs1795380960","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490342,"source":"dbSNP","strand":1,"feature_type":"variation","end":140490342,"alleles":["C","A"]},{"strand":1,"feature_type":"variation","end":140490343,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490343,"source":"dbSNP","seq_region_name":"7","id":"rs1226864614","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795380992","clinical_significance":[],"strand":1,"feature_type":"variation","end":140490347,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490347,"source":"dbSNP"},{"source":"dbSNP","start":140490348,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140490348,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1362505298"},{"id":"rs1302473706","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140490359,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490359,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795381054","source":"dbSNP","start":140490361,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140490361,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140490362,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140490362,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1298145528"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490364,"source":"dbSNP","strand":1,"feature_type":"variation","end":140490364,"alleles":["G","C"],"seq_region_name":"7","id":"rs1332124181","clinical_significance":[]},{"source":"dbSNP","start":140490365,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140490365,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795381109","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1439061702","source":"dbSNP","start":140490376,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140490376,"feature_type":"variation","strand":1},{"id":"rs1273440625","seq_region_name":"7","clinical_significance":[],"end":140490380,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140490380,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1388843044","end":140490382,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140490382,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795381190","clinical_significance":[],"end":140490385,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140490385,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490386,"source":"dbSNP","strand":1,"feature_type":"variation","end":140490386,"alleles":["G","A"],"seq_region_name":"7","id":"rs1366541989","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1240395631","feature_type":"variation","strand":1,"end":140490387,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490387},{"start":140490389,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140490389,"strand":1,"feature_type":"variation","id":"rs1350909790","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140490391,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C","T"],"end":140490391,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs11773605"},{"end":140490392,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140490392,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795381399","clinical_significance":[]},{"start":140490396,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140490396,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795381421","clinical_significance":[]},{"seq_region_name":"7","id":"rs1160694220","clinical_significance":[],"strand":1,"feature_type":"variation","end":140490414,"alleles":["TTTTATTTTTATTTTTA","TTTTATTTTTA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490398,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1585515701","clinical_significance":[],"alleles":["T","A"],"end":140490404,"strand":1,"feature_type":"variation","start":140490404,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs2130405835","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490408,"source":"dbSNP","strand":1,"feature_type":"variation","end":140490408,"alleles":["A","C"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490409,"source":"dbSNP","strand":1,"feature_type":"variation","end":140490409,"alleles":["T","C"],"seq_region_name":"7","id":"rs1455358770","clinical_significance":[]},{"end":140490415,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140490415,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795381503","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795381524","clinical_significance":[],"start":140490419,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140490419,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"end":140490420,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140490420,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1048700887"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490424,"feature_type":"variation","strand":1,"end":140490424,"alleles":["A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1176561553"},{"seq_region_name":"7","id":"rs1434620065","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","-"],"end":140490425,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490425,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585515711","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490427,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140490427},{"clinical_significance":[],"id":"rs1795381597","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490429,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140490429},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795381612","source":"dbSNP","start":140490436,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140490436,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs558743280","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490437,"feature_type":"variation","strand":1,"end":140490439,"alleles":["CCC","CC"]},{"alleles":["G","A","T"],"end":140490442,"feature_type":"variation","strand":1,"source":"dbSNP","start":140490442,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1265198725","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490446,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C","T"],"end":140490446,"id":"rs1453248304","seq_region_name":"7","clinical_significance":[]},{"start":140490449,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140490449,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1196548460","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795381716","alleles":["G","A"],"end":140490453,"feature_type":"variation","strand":1,"source":"dbSNP","start":140490453,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140490455,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140490455,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130405866","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1206880227","alleles":["GG","G"],"end":140490456,"feature_type":"variation","strand":1,"source":"dbSNP","start":140490455,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140490459,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140490459,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs1328778430","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130405873","source":"dbSNP","start":140490460,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140490460,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130405874","end":140490464,"alleles":["-","TCATAC"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140490465,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140490467,"alleles":["G","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490467,"source":"dbSNP","seq_region_name":"7","id":"rs2130405878","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1256771106","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140490469,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490469},{"seq_region_name":"7","id":"rs540983352","clinical_significance":[],"start":140490470,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140490470,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140490473,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490473,"source":"dbSNP","seq_region_name":"7","id":"rs1235898497","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490474,"feature_type":"variation","strand":1,"end":140490474,"alleles":["T","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs553072349"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1310755108","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140490478,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490478},{"seq_region_name":"7","id":"rs1795381852","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140490482,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490482,"source":"dbSNP"},{"clinical_significance":[],"id":"rs183715541","seq_region_name":"7","end":140490489,"alleles":["T","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140490489,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140490490,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490490,"source":"dbSNP","id":"rs1436510945","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","A"],"end":140490492,"feature_type":"variation","strand":1,"source":"dbSNP","start":140490492,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585515730"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1367942072","source":"dbSNP","start":140490498,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140490498,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490499,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140490499,"seq_region_name":"7","id":"rs1585515732","clinical_significance":[]},{"seq_region_name":"7","id":"rs541944413","clinical_significance":[],"start":140490500,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140490500,"alleles":["G","A","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795381969","alleles":["C","T"],"end":140490506,"feature_type":"variation","strand":1,"source":"dbSNP","start":140490506,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490507,"feature_type":"variation","strand":1,"end":140490507,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795381985"},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140490508,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490508,"source":"dbSNP","seq_region_name":"7","id":"rs1477844478","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795382017","source":"dbSNP","start":140490510,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140490510,"feature_type":"variation","strand":1},{"alleles":["T","C"],"end":140490512,"feature_type":"variation","strand":1,"source":"dbSNP","start":140490512,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795382035"},{"start":140490516,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140490516,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1321995204","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140490519,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490519,"source":"dbSNP","id":"rs1795382069","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140490520,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490520,"source":"dbSNP","seq_region_name":"7","id":"rs1795382085","clinical_significance":[]},{"source":"dbSNP","start":140490521,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140490521,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1179530002"},{"clinical_significance":[],"id":"rs1795382119","seq_region_name":"7","end":140490521,"alleles":["T","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140490521,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140490522,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140490522,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1382349737","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490524,"source":"dbSNP","strand":1,"feature_type":"variation","end":140490524,"alleles":["G","A"],"seq_region_name":"7","id":"rs1383795358","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795382184","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490526,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140490526},{"seq_region_name":"7","id":"rs577054544","clinical_significance":[],"start":140490534,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140490534,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140490536,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490536,"clinical_significance":[],"seq_region_name":"7","id":"rs1795382220"},{"source":"dbSNP","start":140490537,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140490537,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs11762588"},{"seq_region_name":"7","id":"rs1467249136","clinical_significance":[],"end":140490539,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140490539,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["G","C"],"end":140490540,"feature_type":"variation","strand":1,"source":"dbSNP","start":140490540,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795382322","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140490541,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490541,"source":"dbSNP","id":"rs1172749859","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490541,"feature_type":"variation","strand":1,"alleles":["C","CGTGCACCACC"],"end":140490541,"clinical_significance":[],"seq_region_name":"7","id":"rs1375786460"},{"seq_region_name":"7","id":"rs1795382361","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490541,"source":"dbSNP","strand":1,"feature_type":"variation","end":140490542,"alleles":["CA","-"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs11763994","alleles":["A","C","G","T"],"end":140490542,"feature_type":"variation","strand":1,"source":"dbSNP","start":140490542,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1795382451","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490543,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140490543},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490544,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140490544,"clinical_significance":[],"seq_region_name":"7","id":"rs1446438515"},{"end":140490545,"alleles":["C","CCC"],"strand":1,"feature_type":"variation","start":140490545,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795382474","clinical_significance":[]},{"seq_region_name":"7","id":"rs1407563223","clinical_significance":[],"start":140490546,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140490546,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795382504","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490547,"feature_type":"variation","strand":1,"end":140490547,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1795382520","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490548,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140490548},{"end":140490552,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140490552,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795382539","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1425662093","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490553,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140490553},{"clinical_significance":[],"seq_region_name":"7","id":"rs1202463106","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490554,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140490554},{"clinical_significance":[],"seq_region_name":"7","id":"rs1322046841","feature_type":"variation","strand":1,"end":140490556,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490556},{"seq_region_name":"7","id":"rs2130406001","clinical_significance":[],"end":140490557,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140490557,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs2130406004","clinical_significance":[],"strand":1,"feature_type":"variation","end":140490558,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490558,"source":"dbSNP"},{"alleles":["A","C"],"end":140490562,"feature_type":"variation","strand":1,"source":"dbSNP","start":140490562,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1349635991"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1280125407","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490565,"feature_type":"variation","strand":1,"end":140490565,"alleles":["T","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795382635","source":"dbSNP","start":140490567,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140490567,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140490571,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490571,"source":"dbSNP","seq_region_name":"7","id":"rs1585515771","clinical_significance":[]},{"seq_region_name":"7","id":"rs1229530228","clinical_significance":[],"end":140490575,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140490575,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs11764909","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490579,"feature_type":"variation","strand":1,"end":140490579,"alleles":["T","A","C","G"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490580,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140490580,"seq_region_name":"7","id":"rs1795382771","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490587,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140490587,"clinical_significance":[],"seq_region_name":"7","id":"rs887376519"},{"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140490588,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490588,"source":"dbSNP","seq_region_name":"7","id":"rs1311012271","clinical_significance":[]},{"source":"dbSNP","start":140490589,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140490589,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs186352162","seq_region_name":"7"},{"end":140490591,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140490591,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1397459501","seq_region_name":"7","clinical_significance":[]},{"id":"rs1374108536","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140490593,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490593,"source":"dbSNP"},{"seq_region_name":"7","id":"rs191817162","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490594,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140490594},{"feature_type":"variation","strand":1,"end":140490594,"alleles":["G","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490594,"clinical_significance":[],"id":"rs1795382917","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1430124770","source":"dbSNP","start":140490607,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140490607,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1284258694","seq_region_name":"7","source":"dbSNP","start":140490609,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140490609,"alleles":["C","T"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140490611,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140490611,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1358442305"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140490618,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490618,"clinical_significance":[],"id":"rs1795383006","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490619,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140490619,"clinical_significance":[],"seq_region_name":"7","id":"rs1795383029"},{"seq_region_name":"7","id":"rs1795383051","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140490620,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490620,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140490623,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490623,"source":"dbSNP","seq_region_name":"7","id":"rs1207953834","clinical_significance":[]},{"clinical_significance":[],"id":"rs1369199702","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490625,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140490625},{"clinical_significance":[],"id":"rs2130406069","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490628,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140490628},{"clinical_significance":[],"seq_region_name":"7","id":"rs1189676164","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490632,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140490632},{"id":"rs1289008553","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490633,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140490633},{"alleles":["CA","-"],"end":140490635,"strand":1,"feature_type":"variation","start":140490634,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1257024197","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490637,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140490637,"clinical_significance":[],"id":"rs1795383176","seq_region_name":"7"},{"id":"rs1458063396","seq_region_name":"7","clinical_significance":[],"end":140490638,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140490638,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140490640,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","start":140490640,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs530532346","clinical_significance":[]},{"alleles":["A","-"],"end":140490640,"strand":1,"feature_type":"variation","start":140490640,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1484207492","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795383241","source":"dbSNP","start":140490640,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140490640,"alleles":["A","AA"],"feature_type":"variation","strand":1},{"end":140490640,"alleles":["-","ACC","ACCC"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140490641,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795383276","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1246293057","clinical_significance":[],"start":140490641,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140490641,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795383310","source":"dbSNP","start":140490641,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","CACCCC"],"end":140490641,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490641,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CCCCCCC","CCCCCC","CCCCCCCC","CCCCCCCCCCCCCC","CCCCCCCCCCCCCCCCCCC","CCCCCCCCCCCCCCCCCCCCCCCCCCC"],"end":140490647,"seq_region_name":"7","id":"rs200256684","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795383411","clinical_significance":[],"end":140490642,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140490642,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1338371285","source":"dbSNP","start":140490645,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["CCCACCCCCCTTCAGTCTCCCA","CCCA"],"end":140490666,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1200233707","seq_region_name":"7","source":"dbSNP","start":140490646,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140490646,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs117840017","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","G","T"],"end":140490647,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490647,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1362188850","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490648,"feature_type":"variation","strand":1,"end":140490648,"alleles":["A","C","G","T"]},{"clinical_significance":[],"id":"rs1409349962","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490648,"feature_type":"variation","strand":1,"alleles":["A","-"],"end":140490648},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795383568","alleles":["CCCCCC","CCCCCCC"],"end":140490654,"feature_type":"variation","strand":1,"source":"dbSNP","start":140490649,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","T"],"end":140490650,"strand":1,"feature_type":"variation","start":140490650,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795383590","clinical_significance":[]},{"id":"rs1417429346","seq_region_name":"7","clinical_significance":[],"start":140490651,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140490651,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1178172054","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140490652,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490652,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490653,"source":"dbSNP","strand":1,"feature_type":"variation","end":140490653,"alleles":["C","A","G","T"],"seq_region_name":"7","id":"rs116245131","clinical_significance":[]},{"end":140490654,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140490654,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1250115615","clinical_significance":[]},{"end":140490655,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140490655,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1226693289"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795383958","feature_type":"variation","strand":1,"end":140490656,"alleles":["TT","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490655},{"strand":1,"feature_type":"variation","alleles":["TTCAGT","-"],"end":140490660,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490655,"source":"dbSNP","seq_region_name":"7","id":"rs1585515862","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140490656,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490656,"source":"dbSNP","id":"rs1162015469","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140490657,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490657,"source":"dbSNP","seq_region_name":"7","id":"rs1181509547","clinical_significance":[]},{"start":140490658,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140490658,"strand":1,"feature_type":"variation","id":"rs1466471703","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140490660,"alleles":["AGT","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490658,"clinical_significance":[],"seq_region_name":"7","id":"rs1413648388"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140490660,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490660,"clinical_significance":[],"id":"rs1795384124","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1397741540","clinical_significance":[],"start":140490661,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140490661,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140490662,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490662,"clinical_significance":[],"seq_region_name":"7","id":"rs1445551025"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1334288058","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490666,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140490666},{"id":"rs2130406181","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140490669,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490669,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490670,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140490670,"clinical_significance":[],"seq_region_name":"7","id":"rs1795384242"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1341777163","source":"dbSNP","start":140490671,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140490671,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1241926299","clinical_significance":[],"end":140490674,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140490674,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140490677,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140490677,"alleles":["A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1331959888","clinical_significance":[]},{"start":140490681,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140490681,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1271977662","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795384361","seq_region_name":"7","source":"dbSNP","start":140490686,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140490686,"alleles":["A","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs565651860","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490687,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140490687},{"end":140490693,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140490693,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs528370265"},{"source":"dbSNP","start":140490700,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140490700,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795384464"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490703,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140490703,"seq_region_name":"7","id":"rs1795384482","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1028731176","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490704,"feature_type":"variation","strand":1,"end":140490704,"alleles":["C","G"]},{"seq_region_name":"7","id":"rs546944234","clinical_significance":[],"strand":1,"feature_type":"variation","end":140490705,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490705,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795384564","alleles":["A","G"],"end":140490707,"feature_type":"variation","strand":1,"source":"dbSNP","start":140490707,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1441155964","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140490708,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490708},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490726,"feature_type":"variation","strand":1,"end":140490726,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1715205086"},{"alleles":["T","C"],"end":140490735,"feature_type":"variation","strand":1,"source":"dbSNP","start":140490735,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1255906225"},{"seq_region_name":"7","id":"rs6961573","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490736,"source":"dbSNP","strand":1,"feature_type":"variation","end":140490736,"alleles":["T","A","C","G"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490748,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140490748,"clinical_significance":[],"seq_region_name":"7","id":"rs1384991499"},{"source":"dbSNP","start":140490749,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140490749,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1195415670"},{"seq_region_name":"7","id":"rs532389440","clinical_significance":[],"start":140490750,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140490750,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795384841","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140490751,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490751},{"clinical_significance":[],"seq_region_name":"7","id":"rs1444225124","alleles":["G","A"],"end":140490752,"feature_type":"variation","strand":1,"source":"dbSNP","start":140490752,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1158385596","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490755,"feature_type":"variation","strand":1,"end":140490755,"alleles":["T","C"]},{"id":"rs1563103970","seq_region_name":"7","clinical_significance":[],"start":140490756,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140490756,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140490760,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490760,"clinical_significance":[],"seq_region_name":"7","id":"rs1795384921"},{"seq_region_name":"7","id":"rs1478523696","clinical_significance":[],"start":140490763,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140490763,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490764,"feature_type":"variation","strand":1,"end":140490764,"alleles":["T","C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1185423651"},{"strand":1,"feature_type":"variation","end":140490769,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490769,"source":"dbSNP","seq_region_name":"7","id":"rs1237474473","clinical_significance":[]},{"start":140490773,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140490773,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs979255599","clinical_significance":[]},{"alleles":["G","A"],"end":140490774,"strand":1,"feature_type":"variation","start":140490774,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795385054","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","A","G","T"],"end":140490775,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490775,"clinical_significance":[],"seq_region_name":"7","id":"rs6464786"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1208749980","end":140490780,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140490780,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs956631285","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140490782,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490782,"source":"dbSNP"},{"id":"rs1281652647","seq_region_name":"7","clinical_significance":[],"start":140490785,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140490785,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140490786,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490786,"clinical_significance":[],"id":"rs1421895288","seq_region_name":"7"},{"seq_region_name":"7","id":"rs569873889","clinical_significance":[],"alleles":["G","A"],"end":140490787,"strand":1,"feature_type":"variation","start":140490787,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs372885694","seq_region_name":"7","feature_type":"variation","strand":1,"end":140490788,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490788},{"seq_region_name":"7","id":"rs1232080834","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490789,"source":"dbSNP","strand":1,"feature_type":"variation","end":140490789,"alleles":["G","A"]},{"id":"rs1370140757","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140490791,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490791,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1172821698","alleles":["C","T"],"end":140490794,"feature_type":"variation","strand":1,"source":"dbSNP","start":140490794,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["G","A"],"end":140490795,"strand":1,"feature_type":"variation","start":140490795,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1437283837","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490800,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140490800,"seq_region_name":"7","id":"rs1585515952","clinical_significance":[]},{"source":"dbSNP","start":140490800,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140490800,"alleles":["A","AA"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795385538"},{"end":140490802,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140490802,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1195956287"},{"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140490803,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490803,"clinical_significance":[],"id":"rs917951793","seq_region_name":"7"},{"end":140490806,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140490806,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585515958","clinical_significance":[]},{"id":"rs1795385670","seq_region_name":"7","clinical_significance":[],"start":140490808,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140490808,"alleles":["C","A","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs6949345","clinical_significance":[],"end":140490810,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140490810,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1563103987","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140490814,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490814,"source":"dbSNP"},{"source":"dbSNP","start":140490816,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140490816,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs949406124"},{"alleles":["C","A","T"],"end":140490817,"feature_type":"variation","strand":1,"source":"dbSNP","start":140490817,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1332926416","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585515972","end":140490818,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140490818,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1563103990","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490819,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140490819},{"clinical_significance":[],"id":"rs1795385888","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490823,"feature_type":"variation","strand":1,"end":140490823,"alleles":["T","C"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490825,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AA","-"],"end":140490826,"id":"rs1795385911","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130406349","clinical_significance":[],"strand":1,"feature_type":"variation","end":140490826,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490826,"source":"dbSNP"},{"id":"rs1415231903","seq_region_name":"7","clinical_significance":[],"end":140490827,"alleles":["G","-"],"strand":1,"feature_type":"variation","start":140490827,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140490828,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490828,"source":"dbSNP","seq_region_name":"7","id":"rs1341122548","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490830,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140490830,"seq_region_name":"7","id":"rs1427740108","clinical_significance":[]},{"start":140490845,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","G","T"],"end":140490845,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs981292076","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795386070","source":"dbSNP","start":140490846,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140490846,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795386094","clinical_significance":[],"alleles":["C","T"],"end":140490849,"strand":1,"feature_type":"variation","start":140490849,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795386116","clinical_significance":[],"strand":1,"feature_type":"variation","end":140490852,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490852,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490853,"feature_type":"variation","strand":1,"end":140490853,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1391259450"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1401744831","end":140490855,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140490855,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1795386196","seq_region_name":"7","clinical_significance":[],"end":140490863,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140490863,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140490864,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490864,"clinical_significance":[],"seq_region_name":"7","id":"rs1795386216"},{"seq_region_name":"7","id":"rs569292294","clinical_significance":[],"start":140490866,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140490866,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1465824562","clinical_significance":[],"end":140490870,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140490870,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["G","A"],"end":140490871,"feature_type":"variation","strand":1,"source":"dbSNP","start":140490871,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs926708573"},{"source":"dbSNP","start":140490872,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140490872,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1233644682"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1256830353","feature_type":"variation","strand":1,"end":140490873,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490873},{"alleles":["C","T"],"end":140490874,"feature_type":"variation","strand":1,"source":"dbSNP","start":140490874,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs931362465"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490877,"source":"dbSNP","strand":1,"feature_type":"variation","end":140490877,"alleles":["C","T"],"seq_region_name":"7","id":"rs1347388725","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795386785","seq_region_name":"7","source":"dbSNP","start":140490878,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140490878,"alleles":["C","A"],"feature_type":"variation","strand":1},{"alleles":["A","C"],"end":140490879,"strand":1,"feature_type":"variation","start":140490879,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1208386081","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585516005","feature_type":"variation","strand":1,"end":140490881,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490881},{"clinical_significance":[],"id":"rs1347065946","seq_region_name":"7","source":"dbSNP","start":140490882,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140490882,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140490882,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["CCC","CC"],"end":140490884,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795386886","seq_region_name":"7"},{"start":140490883,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140490883,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1048606593","clinical_significance":[]},{"source":"dbSNP","start":140490887,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140490887,"alleles":["C","A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs6949390","seq_region_name":"7"},{"source":"dbSNP","start":140490890,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140490890,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1360013579"},{"seq_region_name":"7","id":"rs1795387014","clinical_significance":[],"start":140490891,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140490891,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"end":140490897,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140490897,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1585516016","seq_region_name":"7","clinical_significance":[]},{"id":"rs1269636969","seq_region_name":"7","clinical_significance":[],"end":140490898,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140490898,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140490899,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140490899,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1585516020","seq_region_name":"7"},{"source":"dbSNP","start":140490903,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140490903,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585516024"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795387208","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140490904,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490904},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490905,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140490905,"seq_region_name":"7","id":"rs1279670835","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490906,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140490906,"clinical_significance":[],"seq_region_name":"7","id":"rs1361096063"},{"seq_region_name":"7","id":"rs1795387311","clinical_significance":[],"strand":1,"feature_type":"variation","end":140490912,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490912,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1311452955","seq_region_name":"7","source":"dbSNP","start":140490913,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140490913,"alleles":["A","G"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490914,"source":"dbSNP","strand":1,"feature_type":"variation","end":140490914,"alleles":["G","T"],"seq_region_name":"7","id":"rs1434451189","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1371741457","feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140490915,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490915},{"end":140490916,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140490916,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1171095456","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140490921,"alleles":["A","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490921,"clinical_significance":[],"id":"rs1488925006","seq_region_name":"7"},{"start":140490925,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140490925,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1416856441","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140490929,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490929,"source":"dbSNP","id":"rs1795387437","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1196503403","clinical_significance":[],"strand":1,"feature_type":"variation","end":140490933,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490933,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1795387470","seq_region_name":"7","end":140490934,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140490934,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140490938,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140490938,"strand":1,"feature_type":"variation","id":"rs1472930092","seq_region_name":"7","clinical_significance":[]},{"start":140490943,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140490943,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1238779019","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490944,"feature_type":"variation","strand":1,"end":140490944,"alleles":["C","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795387521"},{"seq_region_name":"7","id":"rs1585516038","clinical_significance":[],"start":140490946,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140490946,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140490959,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140490959,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795387557","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140490960,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490960,"source":"dbSNP","seq_region_name":"7","id":"rs1795387576","clinical_significance":[]},{"end":140490964,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140490964,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585516069","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1485193590","feature_type":"variation","strand":1,"end":140490965,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490965},{"clinical_significance":[],"seq_region_name":"7","id":"rs887237869","feature_type":"variation","strand":1,"end":140490966,"alleles":["CC","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490965},{"clinical_significance":[],"seq_region_name":"7","id":"rs1275057342","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140490966,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490966},{"start":140490967,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140490967,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs6976355","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490969,"source":"dbSNP","strand":1,"feature_type":"variation","end":140490969,"alleles":["C","T"],"seq_region_name":"7","id":"rs1795387694","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795387710","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490970,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140490970},{"alleles":["A","C"],"end":140490971,"strand":1,"feature_type":"variation","start":140490971,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130406496","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1305687691","source":"dbSNP","start":140490972,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140490972,"alleles":["C","T"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140490976,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140490976,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795387752"},{"start":140490977,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140490977,"strand":1,"feature_type":"variation","id":"rs1428306508","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs28873178","source":"dbSNP","start":140490979,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140490979,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490981,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140490981,"clinical_significance":[],"seq_region_name":"7","id":"rs1795387821"},{"end":140490983,"alleles":["CCC","CCCC"],"strand":1,"feature_type":"variation","start":140490981,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1199943068","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140490988,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490988,"clinical_significance":[],"seq_region_name":"7","id":"rs1228900943"},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140490989,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490989,"source":"dbSNP","seq_region_name":"7","id":"rs1795387877","clinical_significance":[]},{"id":"rs2130406521","seq_region_name":"7","clinical_significance":[],"alleles":["G","C"],"end":140490992,"strand":1,"feature_type":"variation","start":140490992,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795387890","clinical_significance":[],"strand":1,"feature_type":"variation","end":140490995,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140490995,"source":"dbSNP"},{"source":"dbSNP","start":140490997,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140490997,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1381664494"},{"clinical_significance":[],"id":"rs1795387923","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140490999,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140490999},{"clinical_significance":[],"id":"rs1291618977","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491000,"feature_type":"variation","strand":1,"end":140491000,"alleles":["A","G"]},{"end":140491002,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140491002,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1414378289"},{"clinical_significance":[],"seq_region_name":"7","id":"rs940256715","alleles":["T","G"],"end":140491005,"feature_type":"variation","strand":1,"source":"dbSNP","start":140491005,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795387978","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491006,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140491006},{"feature_type":"variation","strand":1,"end":140491008,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491008,"clinical_significance":[],"seq_region_name":"7","id":"rs1795387990"},{"seq_region_name":"7","id":"rs1585516102","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491013,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140491013},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491015,"source":"dbSNP","strand":1,"feature_type":"variation","end":140491015,"alleles":["C","A","T"],"seq_region_name":"7","id":"rs1379076712","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1464220298","source":"dbSNP","start":140491016,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140491016,"alleles":["G","A","C"],"feature_type":"variation","strand":1},{"id":"rs781726406","seq_region_name":"7","clinical_significance":[],"start":140491021,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140491021,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491023,"feature_type":"variation","strand":1,"end":140491023,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1171538485"},{"seq_region_name":"7","id":"rs1360571644","clinical_significance":[],"alleles":["G","A"],"end":140491024,"strand":1,"feature_type":"variation","start":140491024,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1795388108","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140491026,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491026},{"start":140491029,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140491029,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795388127","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140491033,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491033,"source":"dbSNP","seq_region_name":"7","id":"rs1419599647","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795388167","clinical_significance":[],"start":140491034,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140491034,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140491037,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491037,"source":"dbSNP","seq_region_name":"7","id":"rs1185411058","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140491042,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491042,"clinical_significance":[],"seq_region_name":"7","id":"rs1420947304"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795388224","alleles":["G","T"],"end":140491050,"feature_type":"variation","strand":1,"source":"dbSNP","start":140491050,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795388240","clinical_significance":[],"alleles":["A","C"],"end":140491053,"strand":1,"feature_type":"variation","start":140491053,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["T","A"],"end":140491056,"feature_type":"variation","strand":1,"source":"dbSNP","start":140491056,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1252350393"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491058,"feature_type":"variation","strand":1,"end":140491058,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795388261"},{"seq_region_name":"7","id":"rs1196096068","clinical_significance":[],"alleles":["G","T"],"end":140491060,"strand":1,"feature_type":"variation","start":140491060,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1482805310","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491064,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140491064},{"alleles":["A","-"],"end":140491065,"strand":1,"feature_type":"variation","start":140491065,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795388349","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491065,"feature_type":"variation","strand":1,"end":140491074,"alleles":["ATTTATATAT","ATTTATATATTTATATAT"],"clinical_significance":[],"seq_region_name":"7","id":"rs1238180443"},{"feature_type":"variation","strand":1,"alleles":["ATTTATATATAT","AT"],"end":140491076,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491065,"clinical_significance":[],"seq_region_name":"7","id":"rs1479622731"},{"source":"dbSNP","start":140491065,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140491078,"alleles":["ATTTATATATATAT","AT"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1232197516","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491065,"feature_type":"variation","strand":1,"end":140491080,"alleles":["ATTTATATATATATAT","AT"],"clinical_significance":[],"seq_region_name":"7","id":"rs1222437417"},{"seq_region_name":"7","id":"rs1323635883","clinical_significance":[],"strand":1,"feature_type":"variation","end":140491082,"alleles":["ATTTATATATATATATAT","AT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491065,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1271320058","clinical_significance":[],"start":140491065,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140491084,"alleles":["ATTTATATATATATATATAT","AT"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140491086,"alleles":["ATTTATATATATATATATATAT","AT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491065,"clinical_significance":[],"id":"rs1232976742","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795388578","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140491066,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491066,"source":"dbSNP"},{"alleles":["TTT","T","TTTTT"],"end":140491068,"strand":1,"feature_type":"variation","start":140491066,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1330073053","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1296292596","end":140491066,"alleles":["-","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140491067,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1277826527","source":"dbSNP","start":140491067,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140491067,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140491068,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140491068,"alleles":["T","TTATATATAT","TTTAT","TTTATAT","TTTATATAT","TTTATATATAT","TTTATATATATAT","TTTATATATATATAT","TTTATATATATATATAT","TTTATATATATATATATAT","TTTATATATATATATATATAT"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1377199857"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795388717","feature_type":"variation","strand":1,"end":140491068,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491068},{"clinical_significance":[],"id":"rs1554453242","seq_region_name":"7","feature_type":"variation","strand":1,"end":140491070,"alleles":["TAT","TATTTATATATATAT","TATTTATATATATATAT","TATTTATATATATATATAT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491068},{"seq_region_name":"7","id":"rs1795388848","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491068,"source":"dbSNP","strand":1,"feature_type":"variation","end":140491072,"alleles":["TATAT","TATATGTATATAT"]},{"id":"rs372009473","seq_region_name":"7","clinical_significance":[],"start":140491068,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TATATATATATATATATATATATATATATAT","TATATATATATAT","TATATATATATATAT","TATATATATATATATAT","TATATATATATATATATAT","TATATATATATATATATATAT","TATATATATATATATATATATAT","TATATATATATATATATATATATAT","TATATATATATATATATATATATATAT","TATATATATATATATATATATATATATAT","TATATATATATATATATATATATATATATATAT","TATATATATATATATATATATATATATATATATAT","TATATATATATATATATATATATATATATATATATAT","TATATATATATATATATATATATATATATATATATATAT","TATATATATATATATATATATATATATATATATATATATAT","TATATATATATATATATATATATATATATATATATATATATAT","TATATATATATATATATATATATATATATATATATATATATATAT","TATATATATATATATATATATATATATATATATATATATATATATAT","TATATATATATATATATATATATATATATATATATATATATATATATATATAT","TATATATATATATATATATATATATATATATATATATATATATATATATATATATAT"],"end":140491098,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1339694054","feature_type":"variation","strand":1,"alleles":["A","-"],"end":140491069,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491069},{"clinical_significance":[],"id":"rs1387198844","seq_region_name":"7","source":"dbSNP","start":140491069,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140491069,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795389201","clinical_significance":[],"start":140491070,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","TTT"],"end":140491070,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1323321650","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491071,"feature_type":"variation","strand":1,"end":140491071,"alleles":["A","T"]},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140491073,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491073,"source":"dbSNP","seq_region_name":"7","id":"rs1795389305","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795389324","seq_region_name":"7","feature_type":"variation","strand":1,"end":140491080,"alleles":["TATATAT","TATATATTATATAT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491074},{"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140491075,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491075,"clinical_significance":[],"id":"rs1231293530","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491078,"feature_type":"variation","strand":1,"end":140491078,"alleles":["T","TGT"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795389357"},{"end":140491079,"alleles":["A","-"],"strand":1,"feature_type":"variation","start":140491079,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795389377","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795389398","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491079,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["ATATATATATATATATA","-"],"end":140491095},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795389416","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140491080,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491080},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795389429","source":"dbSNP","start":140491080,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140491102,"alleles":["TATATATATATATATATATTTTT","T"],"feature_type":"variation","strand":1},{"id":"rs1795389446","seq_region_name":"7","clinical_significance":[],"alleles":["TATATATATATATATATATTTTTTT","T"],"end":140491104,"strand":1,"feature_type":"variation","start":140491080,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491080,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TATATATATATATATATATTTTTTTTTTT","T"],"end":140491108,"seq_region_name":"7","id":"rs1388954506","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["TATATATATATATATATATTTTTTTTTTTTTT","T"],"end":140491111,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491080,"clinical_significance":[],"seq_region_name":"7","id":"rs1290319984"},{"end":140491114,"alleles":["TATATATATATATATATATTTTTTTTTTTTTTTTT","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140491080,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1451139953"},{"seq_region_name":"7","id":"rs1279830958","clinical_significance":[],"alleles":["A","-"],"end":140491081,"strand":1,"feature_type":"variation","start":140491081,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795389545","clinical_significance":[],"start":140491081,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140491081,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140491081,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140491091,"alleles":["ATATATATATA","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795389595"},{"clinical_significance":[],"id":"rs1795389623","seq_region_name":"7","alleles":["ATATATATATATA","-"],"end":140491093,"feature_type":"variation","strand":1,"source":"dbSNP","start":140491081,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491081,"feature_type":"variation","strand":1,"alleles":["ATATATATATATATATA","-"],"end":140491097,"clinical_significance":[],"seq_region_name":"7","id":"rs1363085175"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140491082,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491082,"source":"dbSNP","seq_region_name":"7","id":"rs1485662141","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491082,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","TT"],"end":140491082,"id":"rs1795389684","seq_region_name":"7","clinical_significance":[]},{"start":140491082,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TATATATATATATATATT","T"],"end":140491099,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1176506564","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1455545711","source":"dbSNP","start":140491082,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TATATATATATATATATTT","T"],"end":140491100,"feature_type":"variation","strand":1},{"start":140491082,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TATATATATATATATATTTT","T"],"end":140491101,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1393122704","clinical_significance":[]},{"alleles":["TATATATATATATATATTTTT","T"],"end":140491102,"feature_type":"variation","strand":1,"source":"dbSNP","start":140491082,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1193122344"},{"seq_region_name":"7","id":"rs1795389808","clinical_significance":[],"end":140491104,"alleles":["TATATATATATATATATTTTTTT","T"],"strand":1,"feature_type":"variation","start":140491082,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1450110199","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491082,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TATATATATATATATATTTTTTTTTTT","T"],"end":140491108},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795389866","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491082,"feature_type":"variation","strand":1,"alleles":["TATATATATATATATATTTTTTTTTTTT","T"],"end":140491109},{"clinical_significance":[],"seq_region_name":"7","id":"rs1263918196","end":140491110,"alleles":["TATATATATATATATATTTTTTTTTTTTT","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140491082,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1203651064","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491082,"source":"dbSNP","strand":1,"feature_type":"variation","end":140491112,"alleles":["TATATATATATATATATTTTTTTTTTTTTTT","T"]},{"strand":1,"feature_type":"variation","end":140491083,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491083,"source":"dbSNP","seq_region_name":"7","id":"rs1585516181","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","-"],"end":140491083,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491083,"source":"dbSNP","seq_region_name":"7","id":"rs1795389985","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795390003","feature_type":"variation","strand":1,"end":140491085,"alleles":["ATA","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491083},{"clinical_significance":[],"id":"rs1563104074","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491083,"feature_type":"variation","strand":1,"alleles":["ATATATA","-"],"end":140491089},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491083,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["ATATATATATA","-"],"end":140491093,"id":"rs1563104080","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1257010942","clinical_significance":[],"start":140491083,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["ATATATATATATATA","-"],"end":140491097,"strand":1,"feature_type":"variation"},{"start":140491084,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140491084,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1373581457","clinical_significance":[]},{"source":"dbSNP","start":140491084,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140491086,"alleles":["TAT","TATGTAT"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795390155"},{"alleles":["TATATATATATATATT","T"],"end":140491099,"strand":1,"feature_type":"variation","start":140491084,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1563104086","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1212611310","clinical_significance":[],"start":140491084,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140491100,"alleles":["TATATATATATATATTT","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1346342914","alleles":["TATATATATATATATTTT","T"],"end":140491101,"feature_type":"variation","strand":1,"source":"dbSNP","start":140491084,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["TATATATATATATATTTTT","T"],"end":140491102,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491084,"clinical_significance":[],"id":"rs1303258658","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1229765527","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491084,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TATATATATATATATTTTTT","T"],"end":140491103},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491084,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TATATATATATATATTTTTTT","T"],"end":140491104,"seq_region_name":"7","id":"rs1563104095","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1365350673","source":"dbSNP","start":140491084,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140491105,"alleles":["TATATATATATATATTTTTTTT","T"],"feature_type":"variation","strand":1},{"alleles":["TATATATATATATATTTTTTTTT","T"],"end":140491106,"strand":1,"feature_type":"variation","start":140491084,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1297096734","clinical_significance":[]},{"clinical_significance":[],"id":"rs1380231304","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491084,"feature_type":"variation","strand":1,"end":140491108,"alleles":["TATATATATATATATTTTTTTTTTT","T"]},{"start":140491084,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TATATATATATATATTTTTTTTTTTT","T"],"end":140491109,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1383725330","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795390462","source":"dbSNP","start":140491084,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TATATATATATATATTTTTTTTTTTTT","T"],"end":140491110,"feature_type":"variation","strand":1},{"end":140491111,"alleles":["TATATATATATATATTTTTTTTTTTTTT","T"],"strand":1,"feature_type":"variation","start":140491084,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1563104100","clinical_significance":[]},{"source":"dbSNP","start":140491084,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TATATATATATATATTTTTTTTTTTTTTT","T"],"end":140491112,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1303216578"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491084,"source":"dbSNP","strand":1,"feature_type":"variation","end":140491113,"alleles":["TATATATATATATATTTTTTTTTTTTTTTT","T"],"seq_region_name":"7","id":"rs1436312886","clinical_significance":[]},{"id":"rs1795390543","seq_region_name":"7","clinical_significance":[],"end":140491127,"alleles":["TATATATATATATATTTTTTTTTTTTTTTTTTTTTTTAATAAGC","-"],"strand":1,"feature_type":"variation","start":140491084,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1585516220","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491085,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140491085},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491085,"feature_type":"variation","strand":1,"end":140491085,"alleles":["A","-"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795390576"},{"seq_region_name":"7","id":"rs1563104108","clinical_significance":[],"end":140491087,"alleles":["ATA","-"],"strand":1,"feature_type":"variation","start":140491085,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140491085,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140491089,"alleles":["ATATA","-"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1172987078","clinical_significance":[]},{"alleles":["ATATATA","-"],"end":140491091,"feature_type":"variation","strand":1,"source":"dbSNP","start":140491085,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1430294797","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795390646","alleles":["ATATATATA","-"],"end":140491093,"feature_type":"variation","strand":1,"source":"dbSNP","start":140491085,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140491095,"alleles":["ATATATATATA","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140491085,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1563104118"},{"clinical_significance":[],"id":"rs1374926360","seq_region_name":"7","source":"dbSNP","start":140491085,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140491097,"alleles":["ATATATATATATA","-"],"feature_type":"variation","strand":1},{"id":"rs1795390703","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491086,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","TT","TTT","TTTT"],"end":140491086},{"source":"dbSNP","start":140491086,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TATATATATATATT","T"],"end":140491099,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1191094093"},{"clinical_significance":[],"id":"rs1428153772","seq_region_name":"7","end":140491100,"alleles":["TATATATATATATTT","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140491086,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140491101,"alleles":["TATATATATATATTTT","T"],"strand":1,"feature_type":"variation","start":140491086,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1257038313","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1190547378","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491086,"feature_type":"variation","strand":1,"alleles":["TATATATATATATTTTT","T"],"end":140491102},{"clinical_significance":[],"seq_region_name":"7","id":"rs1484925948","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491086,"feature_type":"variation","strand":1,"end":140491103,"alleles":["TATATATATATATTTTTT","T"]},{"end":140491104,"alleles":["TATATATATATATTTTTTT","T","TATATATATATATTTTTTTATATATATATATTTTTTT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140491086,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs201435888"},{"seq_region_name":"7","id":"rs1206587948","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["TATATATATATATTTTTTTT","T"],"end":140491105,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491086,"source":"dbSNP"},{"end":140491106,"alleles":["TATATATATATATTTTTTTTT","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140491086,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1342073359"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491086,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TATATATATATATTTTTTTTTTT","T"],"end":140491108,"seq_region_name":"7","id":"rs1252570452","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491086,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TATATATATATATTTTTTTTTTTT","T"],"end":140491109,"seq_region_name":"7","id":"rs1224530328","clinical_significance":[]},{"seq_region_name":"7","id":"rs1325522054","clinical_significance":[],"start":140491086,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TATATATATATATTTTTTTTTTTTT","T"],"end":140491110,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1398469686","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491087,"feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140491087},{"strand":1,"feature_type":"variation","end":140491087,"alleles":["A","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491087,"source":"dbSNP","seq_region_name":"7","id":"rs1563104130","clinical_significance":[]},{"seq_region_name":"7","id":"rs1312929039","clinical_significance":[],"start":140491087,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["ATA","-"],"end":140491089,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491087,"feature_type":"variation","strand":1,"alleles":["ATATA","-"],"end":140491091,"clinical_significance":[],"seq_region_name":"7","id":"rs1416218091"},{"start":140491087,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140491091,"alleles":["ATATA","ATATAGATATAGATATA"],"strand":1,"feature_type":"variation","id":"rs1795391003","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1353371624","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491087,"source":"dbSNP","strand":1,"feature_type":"variation","end":140491093,"alleles":["ATATATA","-"]},{"strand":1,"feature_type":"variation","alleles":["ATATATATA","-"],"end":140491095,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491087,"source":"dbSNP","seq_region_name":"7","id":"rs1312040864","clinical_significance":[]},{"seq_region_name":"7","id":"rs1430394233","clinical_significance":[],"alleles":["ATATATATATA","-"],"end":140491097,"strand":1,"feature_type":"variation","start":140491087,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140491088,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140491088,"alleles":["T","TT","TTT","TTTT","TTTTT"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795391103"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1166233040","end":140491099,"alleles":["TATATATATATT","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140491088,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1461506522","seq_region_name":"7","alleles":["TATATATATATTT","T"],"end":140491100,"feature_type":"variation","strand":1,"source":"dbSNP","start":140491088,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["TATATATATATTTT","T"],"end":140491101,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491088,"source":"dbSNP","seq_region_name":"7","id":"rs1795391175","clinical_significance":[]},{"id":"rs1369288219","seq_region_name":"7","clinical_significance":[],"start":140491088,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TATATATATATTTTT","T"],"end":140491102,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1167427178","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491088,"feature_type":"variation","strand":1,"end":140491103,"alleles":["TATATATATATTTTTT","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491088,"feature_type":"variation","strand":1,"end":140491104,"alleles":["TATATATATATTTTTTT","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1474349284"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491088,"source":"dbSNP","strand":1,"feature_type":"variation","end":140491105,"alleles":["TATATATATATTTTTTTT","T"],"seq_region_name":"7","id":"rs1257332567","clinical_significance":[]},{"id":"rs1183276578","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140491106,"alleles":["TATATATATATTTTTTTTT","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491088,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1440064794","clinical_significance":[],"alleles":["TATATATATATTTTTTTTTT","T"],"end":140491107,"strand":1,"feature_type":"variation","start":140491088,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491088,"feature_type":"variation","strand":1,"end":140491108,"alleles":["TATATATATATTTTTTTTTTT","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1248987704"},{"strand":1,"feature_type":"variation","end":140491109,"alleles":["TATATATATATTTTTTTTTTTT","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491088,"source":"dbSNP","seq_region_name":"7","id":"rs1193595997","clinical_significance":[]},{"end":140491110,"alleles":["TATATATATATTTTTTTTTTTTT","T"],"strand":1,"feature_type":"variation","start":140491088,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1338235767","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491089,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140491089,"clinical_significance":[],"seq_region_name":"7","id":"rs1410130294"},{"clinical_significance":[],"id":"rs1563104141","seq_region_name":"7","alleles":["A","-"],"end":140491089,"feature_type":"variation","strand":1,"source":"dbSNP","start":140491089,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["A","ACA"],"end":140491089,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491089,"source":"dbSNP","seq_region_name":"7","id":"rs1795391399","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["ATA","-"],"end":140491091,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491089,"source":"dbSNP","seq_region_name":"7","id":"rs1273236092","clinical_significance":[]},{"seq_region_name":"7","id":"rs1234821529","clinical_significance":[],"strand":1,"feature_type":"variation","end":140491093,"alleles":["ATATA","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491089,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795391472","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491089,"feature_type":"variation","strand":1,"end":140491095,"alleles":["ATATATA","-"]},{"clinical_significance":[],"id":"rs1332199952","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491089,"feature_type":"variation","strand":1,"alleles":["ATATATATA","-"],"end":140491097},{"feature_type":"variation","strand":1,"end":140491090,"alleles":["T","TT","TTT","TTTT","TTTTT","TTTTTTTT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491090,"clinical_significance":[],"seq_region_name":"7","id":"rs1292459515"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795391514","end":140491090,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140491090,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795391561","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491090,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TAT","TATGTAT"],"end":140491092},{"end":140491099,"alleles":["TATATATATT","T"],"strand":1,"feature_type":"variation","start":140491090,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795391586","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1337493032","alleles":["TATATATATTT","T"],"end":140491100,"feature_type":"variation","strand":1,"source":"dbSNP","start":140491090,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1326710055","feature_type":"variation","strand":1,"alleles":["TATATATATTTT","T"],"end":140491101,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491090},{"alleles":["TATATATATTTTT","T"],"end":140491102,"strand":1,"feature_type":"variation","start":140491090,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1390722632","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["TATATATATTTTTT","T"],"end":140491103,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491090,"clinical_significance":[],"id":"rs1391631874","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1327993764","clinical_significance":[],"alleles":["TATATATATTTTTTT","T"],"end":140491104,"strand":1,"feature_type":"variation","start":140491090,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1460086886","clinical_significance":[],"start":140491090,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TATATATATTTTTTTT","T"],"end":140491105,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1417339178","feature_type":"variation","strand":1,"end":140491106,"alleles":["TATATATATTTTTTTTT","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491090},{"seq_region_name":"7","id":"rs1160415794","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491090,"source":"dbSNP","strand":1,"feature_type":"variation","end":140491107,"alleles":["TATATATATTTTTTTTTT","T"]},{"end":140491108,"alleles":["TATATATATTTTTTTTTTT","T"],"strand":1,"feature_type":"variation","start":140491090,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1471334050","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["TATATATATTTTTTTTTTTT","T"],"end":140491109,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491090,"clinical_significance":[],"seq_region_name":"7","id":"rs1362401736"},{"id":"rs1181767306","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491090,"source":"dbSNP","strand":1,"feature_type":"variation","end":140491110,"alleles":["TATATATATTTTTTTTTTTTT","T"]},{"seq_region_name":"7","id":"rs1452688359","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491090,"source":"dbSNP","strand":1,"feature_type":"variation","end":140491113,"alleles":["TATATATATTTTTTTTTTTTTTTT","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1224147165","source":"dbSNP","start":140491091,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140491091,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563104155","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491091,"feature_type":"variation","strand":1,"end":140491091,"alleles":["A","-"]},{"seq_region_name":"7","id":"rs1795391881","clinical_significance":[],"start":140491091,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","AGATATAGA"],"end":140491091,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140491091,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["ATA","-"],"end":140491093,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1253148303"},{"clinical_significance":[],"id":"rs1214950225","seq_region_name":"7","source":"dbSNP","start":140491091,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140491095,"alleles":["ATATA","-"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1466859963","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["ATATATA","-"],"end":140491097,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491091,"source":"dbSNP"},{"alleles":["T","TT","TTT","TTTT","TTTTT"],"end":140491092,"strand":1,"feature_type":"variation","start":140491092,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1272100255","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795391963","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491092,"source":"dbSNP","strand":1,"feature_type":"variation","end":140491092,"alleles":["T","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795392028","alleles":["TAT","TATGTAT"],"end":140491094,"feature_type":"variation","strand":1,"source":"dbSNP","start":140491092,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1352631046","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491092,"feature_type":"variation","strand":1,"alleles":["TATATATT","T"],"end":140491099},{"start":140491092,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TATATATTT","T"],"end":140491100,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1277555067","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795392118","feature_type":"variation","strand":1,"alleles":["TATATATTTT","T"],"end":140491101,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491092},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491092,"feature_type":"variation","strand":1,"end":140491102,"alleles":["TATATATTTTT","T"],"clinical_significance":[],"id":"rs1238320234","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1371571456","feature_type":"variation","strand":1,"alleles":["TATATATTTTTT","T"],"end":140491103,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491092},{"end":140491104,"alleles":["TATATATTTTTTT","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140491092,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1305728995"},{"source":"dbSNP","start":140491092,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TATATATTTTTTTT","T"],"end":140491105,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795392226"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1438756212","alleles":["TATATATTTTTTTTT","T"],"end":140491106,"feature_type":"variation","strand":1,"source":"dbSNP","start":140491092,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1394057232","feature_type":"variation","strand":1,"alleles":["TATATATTTTTTTTTT","T"],"end":140491107,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491092},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491092,"feature_type":"variation","strand":1,"alleles":["TATATATTTTTTTTTTT","T"],"end":140491108,"clinical_significance":[],"seq_region_name":"7","id":"rs1321523592"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491092,"feature_type":"variation","strand":1,"end":140491109,"alleles":["TATATATTTTTTTTTTTT","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1402637124"},{"seq_region_name":"7","id":"rs1383341336","clinical_significance":[],"strand":1,"feature_type":"variation","end":140491110,"alleles":["TATATATTTTTTTTTTTTT","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491092,"source":"dbSNP"},{"id":"rs1795392377","seq_region_name":"7","clinical_significance":[],"alleles":["TATATATTTTTTTTTTTTTT","T"],"end":140491111,"strand":1,"feature_type":"variation","start":140491092,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1041295270","feature_type":"variation","strand":1,"end":140491112,"alleles":["TATATATTTTTTTTTTTTTTT","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491092},{"seq_region_name":"7","id":"rs1451977630","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140491093,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491093,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1478650447","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491093,"feature_type":"variation","strand":1,"alleles":["A","-"],"end":140491093},{"source":"dbSNP","start":140491093,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["ATA","-"],"end":140491095,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1397353303","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1194984874","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491093,"source":"dbSNP","strand":1,"feature_type":"variation","end":140491097,"alleles":["ATATA","-"]},{"id":"rs1563104177","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140491094,"alleles":["T","TT","TTT","TTTT","TTTTT","TTTTTT","TTTTTTT","TTTTTTTTT","TTTTTTTTTT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491094,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1251806572","seq_region_name":"7","source":"dbSNP","start":140491094,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140491099,"alleles":["TATATT","T"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140491100,"alleles":["TATATTT","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491094,"clinical_significance":[],"seq_region_name":"7","id":"rs1216151920"},{"clinical_significance":[],"id":"rs1448360030","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491094,"feature_type":"variation","strand":1,"alleles":["TATATTTT","T"],"end":140491101},{"seq_region_name":"7","id":"rs1281908114","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491094,"source":"dbSNP","strand":1,"feature_type":"variation","end":140491102,"alleles":["TATATTTTT","T"]},{"source":"dbSNP","start":140491094,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TATATTTTTT","T"],"end":140491103,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1204263470"},{"strand":1,"feature_type":"variation","alleles":["TATATTTTTTT","T"],"end":140491104,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491094,"source":"dbSNP","seq_region_name":"7","id":"rs1348542755","clinical_significance":[]},{"clinical_significance":[],"id":"rs1305472304","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491094,"feature_type":"variation","strand":1,"alleles":["TATATTTTTTTT","T"],"end":140491105},{"start":140491094,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140491106,"alleles":["TATATTTTTTTTT","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1231965681","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140491107,"alleles":["TATATTTTTTTTTT","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491094,"source":"dbSNP","seq_region_name":"7","id":"rs1370395369","clinical_significance":[]},{"end":140491108,"alleles":["TATATTTTTTTTTTT","T"],"strand":1,"feature_type":"variation","start":140491094,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1270840515","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["TATATTTTTTTTTTTT","T"],"end":140491109,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491094,"clinical_significance":[],"seq_region_name":"7","id":"rs1795392902"},{"strand":1,"feature_type":"variation","alleles":["TATATTTTTTTTTTTTT","T"],"end":140491110,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491094,"source":"dbSNP","seq_region_name":"7","id":"rs1433222635","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["TATATTTTTTTTTTTTTT","T"],"end":140491111,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491094,"source":"dbSNP","seq_region_name":"7","id":"rs1795392963","clinical_significance":[]},{"start":140491094,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TATATTTTTTTTTTTTTTT","T"],"end":140491112,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795392987","clinical_significance":[]},{"start":140491095,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140491095,"alleles":["A","-"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1354528763","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1434605400","feature_type":"variation","strand":1,"alleles":["A","T"],"end":140491095,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491095},{"clinical_significance":[],"seq_region_name":"7","id":"rs1318079538","feature_type":"variation","strand":1,"alleles":["ATA","-"],"end":140491097,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491095},{"end":140491096,"alleles":["T","TT","TTT","TTTT","TTTTT","TTTTTT","TTTTTTTT","TTTTTTTTTT","TTTTTTTTTTT","TTTTTTTTTTTT","TTTTTTTTTTTTT","TTTTTTTTTTTTTT","TTTTTTTTTTTTTTTT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140491096,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1435680554"},{"alleles":["TATT","T"],"end":140491099,"feature_type":"variation","strand":1,"source":"dbSNP","start":140491096,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795393233"},{"seq_region_name":"7","id":"rs1394016146","clinical_significance":[],"end":140491100,"alleles":["TATTT","T"],"strand":1,"feature_type":"variation","start":140491096,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1186536387","end":140491101,"alleles":["TATTTT","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140491096,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1476194771","alleles":["TATTTTT","T"],"end":140491102,"feature_type":"variation","strand":1,"source":"dbSNP","start":140491096,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["TATTTTTT","T"],"end":140491103,"feature_type":"variation","strand":1,"source":"dbSNP","start":140491096,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795393367"},{"alleles":["TATTTTTTT","T"],"end":140491104,"feature_type":"variation","strand":1,"source":"dbSNP","start":140491096,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1239968783"},{"clinical_significance":[],"id":"rs1192232989","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491096,"feature_type":"variation","strand":1,"end":140491105,"alleles":["TATTTTTTTT","T"]},{"start":140491096,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TATTTTTTTTT","T"],"end":140491106,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1330082890","clinical_significance":[]},{"seq_region_name":"7","id":"rs1282161054","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491096,"source":"dbSNP","strand":1,"feature_type":"variation","end":140491107,"alleles":["TATTTTTTTTTT","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491096,"feature_type":"variation","strand":1,"alleles":["TATTTTTTTTTTT","T"],"end":140491108,"clinical_significance":[],"seq_region_name":"7","id":"rs1208725847"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1347039404","feature_type":"variation","strand":1,"end":140491109,"alleles":["TATTTTTTTTTTTT","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491096},{"seq_region_name":"7","id":"rs1273820541","clinical_significance":[],"start":140491096,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TATTTTTTTTTTTTT","T"],"end":140491110,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491096,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TATTTTTTTTTTTTTT","T"],"end":140491111,"id":"rs1795393590","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140491096,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TATTTTTTTTTTTTTTT","T"],"end":140491112,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795393614"},{"alleles":["A","T"],"end":140491097,"feature_type":"variation","strand":1,"source":"dbSNP","start":140491097,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs55881645"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1218808875","alleles":["A","-"],"end":140491097,"feature_type":"variation","strand":1,"source":"dbSNP","start":140491097,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["T","TATATATATATATATATATATTTTTTTTTTTT","TATATATATATATATATATT","TATATATATATATATATATTTTTTTT","TATATATATATATATATT","TATATATATATATATATTT","TATATATATATATATATTTT","TATATATATATATATATTTTTTTT","TATATATATATATATATTTTTTTTTTTTTTT","TATATATATATATATATTTTTTTTTTTTTTTT","TATATATATATATATT","TATATATATATATATTT","TATATATATATATATTTT","TATATATATATATATTTTTT","TATATATATATATATTTTTTT","TATATATATATATATTTTTTTT","TATATATATATATATTTTTTTTT","TATATATATATATATTTTTTTTTTTTT","TATATATATATATATTTTTTTTTTTTTTT","TATATATATATATT","TATATATATATATTT","TATATATATATATTTT","TATATATATATATTTTTT","TATATATATATATTTTTTTT","TATATATATATATTTTTTTTTTTT","TATATATATATATTTTTTTTTTTTT","TATATATATATT","TATATATATATTT","TATATATATATTTT","TATATATATATTTTT","TATATATATATTTTTT","TATATATATATTTTTTT","TATATATATATTTTTTTT","TATATATATATTTTTTTTT","TATATATATATTTTTTTTTTTTTTTTTT","TATATATATT","TATATATATTT","TATATATATTTT","TATATATATTTTT","TATATATATTTTTT","TATATATATTTTTTT","TATATATATTTTTTTT","TATATATATTTTTTTTT","TATATATATTTTTTTTTT","TATATATT","TATATATTT","TATATATTTATTTTTT","TATATATTTT","TATATATTTTT","TATATATTTTTT","TATATATTTTTTT","TATATATTTTTTTT","TATATATTTTTTTTT","TATATATTTTTTTTTT","TATATATTTTTTTTTTTT","TATATCTTTTTTTTTTTT","TATATT","TATATTT","TATATTTT","TATATTTTT","TATATTTTTT","TATATTTTTTT","TATATTTTTTTT","TATATTTTTTTTT","TATATTTTTTTTTT","TATATTTTTTTTTTT","TATT","TATTT","TATTTT","TATTTTT","TATTTTTT","TATTTTTTT","TATTTTTTTT","TATTTTTTTTT","TATTTTTTTTTT","TATTTTTTTTTTT","TATTTTTTTTTTTT","TATTTTTTTTTTTTT"],"end":140491098,"strand":1,"feature_type":"variation","start":140491098,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1195488517","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795393755","end":140491098,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140491098,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795394327","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491098,"feature_type":"variation","strand":1,"alleles":["TTT","TTTATATTTTTTT","TTTATTTTTTTTTT","TTTATTTTTTTTTTT"],"end":140491100},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795394371","feature_type":"variation","strand":1,"alleles":["TTTT","TTTTCTTTT"],"end":140491101,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491098},{"source":"dbSNP","start":140491098,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140491120,"alleles":["TTTTTTTTTTTTTTTTTTTTTTT","TTTTT","TTTTTT","TTTTTTT","TTTTTTTT","TTTTTTTTT","TTTTTTTTTT","TTTTTTTTTTT","TTTTTTTTTTTT","TTTTTTTTTTTTT","TTTTTTTTTTTTTT","TTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs57741072"},{"alleles":["-","A","ATA","ATATA","ATATACATA","ATATATA","ATATATATA","ATATATATATA","ATATATATATATA","ATATATATATATATA","ATATATATATATATATA","ATATATATATATATATATA","ATATATATATATATATATATA","ATATATATATATATATATATATA","ATATATGTATA","ATATTTATA"],"end":140491098,"strand":1,"feature_type":"variation","start":140491099,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1491452491","clinical_significance":[]},{"source":"dbSNP","start":140491099,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140491099,"alleles":["T","A","C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs11765682","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1554453282","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491099,"source":"dbSNP","strand":1,"feature_type":"variation","end":140491099,"alleles":["T","TAAAAAAAAATATATATATATAT"]},{"seq_region_name":"7","id":"rs1563104227","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491100,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["-","A","ATA","ATATA","ATATATA","ATATATATA","ATATATATATATA","ATATATATATATATA","ATATATATATATATATA"],"end":140491099},{"clinical_significance":[],"id":"rs1284509859","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491100,"feature_type":"variation","strand":1,"end":140491100,"alleles":["T","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563104231","alleles":["-","A"],"end":140491100,"feature_type":"variation","strand":1,"source":"dbSNP","start":140491101,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140491101,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491101,"clinical_significance":[],"seq_region_name":"7","id":"rs1214007409"},{"clinical_significance":[],"id":"rs1795395127","seq_region_name":"7","end":140491101,"alleles":["T","TAT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140491101,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795395154","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491101,"source":"dbSNP","strand":1,"feature_type":"variation","end":140491102,"alleles":["TT","TTATT"]},{"seq_region_name":"7","id":"rs1563104233","clinical_significance":[],"alleles":["-","ATATATAAA"],"end":140491101,"strand":1,"feature_type":"variation","start":140491102,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491102,"feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140491102,"clinical_significance":[],"seq_region_name":"7","id":"rs1485825158"},{"id":"rs1210874451","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140491103,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491103,"source":"dbSNP"},{"id":"rs1269888049","seq_region_name":"7","clinical_significance":[],"end":140491104,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140491104,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140491105,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140491105,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1431136483","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491106,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","G"],"end":140491106,"seq_region_name":"7","id":"rs868742547","clinical_significance":[]},{"seq_region_name":"7","id":"rs866049342","clinical_significance":[],"alleles":["T","A"],"end":140491107,"strand":1,"feature_type":"variation","start":140491107,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["T","A","G"],"end":140491108,"strand":1,"feature_type":"variation","start":140491108,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs866911428","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs868627308","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491109,"feature_type":"variation","strand":1,"end":140491109,"alleles":["T","A"]},{"strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140491110,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491110,"source":"dbSNP","seq_region_name":"7","id":"rs1359883642","clinical_significance":[]},{"seq_region_name":"7","id":"rs1563104244","clinical_significance":[],"alleles":["TTTTTTTTTTTA","-"],"end":140491121,"strand":1,"feature_type":"variation","start":140491110,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1458323498","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491111,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140491111},{"feature_type":"variation","strand":1,"end":140491111,"alleles":["T","TCT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491111,"clinical_significance":[],"id":"rs1795395526","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1295107362","feature_type":"variation","strand":1,"alleles":["T","A"],"end":140491112,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491112},{"seq_region_name":"7","id":"rs1563104251","clinical_significance":[],"alleles":["TTTTTTTTTA","-"],"end":140491121,"strand":1,"feature_type":"variation","start":140491112,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140491113,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140491113,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795395613"},{"start":140491114,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140491114,"alleles":["T","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1198182098","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563104254","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491114,"feature_type":"variation","strand":1,"alleles":["TTTTTTTA","-"],"end":140491121},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491115,"source":"dbSNP","strand":1,"feature_type":"variation","end":140491115,"alleles":["T","A","G"],"seq_region_name":"7","id":"rs1429341834","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795395716","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","A"],"end":140491116,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491116},{"clinical_significance":[],"id":"rs1795395741","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491117,"feature_type":"variation","strand":1,"end":140491117,"alleles":["T","G"]},{"end":140491121,"alleles":["TTTA","-"],"strand":1,"feature_type":"variation","start":140491118,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795395767","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491120,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140491120,"clinical_significance":[],"id":"rs1196850016","seq_region_name":"7"},{"id":"rs1554453276","seq_region_name":"7","clinical_significance":[],"start":140491121,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140491120,"alleles":["-","TA","TTA","TTTA","TTTTA","TTTTTA","TTTTTTA","TTTTTTTTA","TTTTTTTTTA","TTTTTTTTTTA","TTTTTTTTTTTATA","TTTTTTTTTTTTA","TTTTTTTTTTTTTTTTA"],"strand":1,"feature_type":"variation"},{"start":140491121,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G","T"],"end":140491121,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs191509666","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795395961","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491121,"source":"dbSNP","strand":1,"feature_type":"variation","end":140491122,"alleles":["AA","AAA"]},{"id":"rs1795395992","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["AA","-"],"end":140491122,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491121,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491122,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140491122,"clinical_significance":[],"seq_region_name":"7","id":"rs1385961912"},{"start":140491123,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140491123,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795396046","clinical_significance":[]},{"end":140491124,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140491124,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1302966595","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1377839735","clinical_significance":[],"start":140491126,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140491126,"alleles":["G","A","T"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491127,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140491127,"id":"rs1242488665","seq_region_name":"7","clinical_significance":[]},{"end":140491129,"alleles":["A","C","G","T"],"strand":1,"feature_type":"variation","start":140491129,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1307161196","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795396183","alleles":["T","A"],"end":140491130,"feature_type":"variation","strand":1,"source":"dbSNP","start":140491130,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140491131,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140491131,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs746209498","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795396242","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491132,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140491132},{"source":"dbSNP","start":140491133,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140491133,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795396276","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795396301","end":140491134,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140491134,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140491135,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491135,"clinical_significance":[],"seq_region_name":"7","id":"rs1316894423"},{"seq_region_name":"7","id":"rs1795396353","clinical_significance":[],"end":140491140,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140491140,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["C","A"],"end":140491141,"feature_type":"variation","strand":1,"source":"dbSNP","start":140491141,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795396372"},{"start":140491143,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140491143,"strand":1,"feature_type":"variation","id":"rs1795396390","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1307740729","clinical_significance":[],"start":140491157,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140491157,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"end":140491160,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140491160,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs901537074","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1380142287","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140491165,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491165,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1339669271","clinical_significance":[],"alleles":["T","C"],"end":140491167,"strand":1,"feature_type":"variation","start":140491167,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1313249291","clinical_significance":[],"start":140491169,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140491169,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140491171,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491171,"source":"dbSNP","seq_region_name":"7","id":"rs2130407466","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140491181,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491181,"clinical_significance":[],"id":"rs1585516460","seq_region_name":"7"},{"source":"dbSNP","start":140491188,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140491188,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795396996"},{"clinical_significance":[],"id":"rs1585516465","seq_region_name":"7","end":140491189,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140491189,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs997175163","source":"dbSNP","start":140491190,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140491190,"alleles":["T","C","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1267715828","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140491196,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491196},{"start":140491199,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140491199,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs375752198","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491200,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140491200,"clinical_significance":[],"seq_region_name":"7","id":"rs1487724034"},{"start":140491201,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140491201,"strand":1,"feature_type":"variation","id":"rs1795397121","seq_region_name":"7","clinical_significance":[]},{"id":"rs1795397139","seq_region_name":"7","clinical_significance":[],"end":140491203,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140491203,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130407498","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491204,"feature_type":"variation","strand":1,"end":140491204,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795397159","source":"dbSNP","start":140491210,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140491210,"alleles":["A","C"],"feature_type":"variation","strand":1},{"id":"rs1213399166","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140491212,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491212,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795397193","source":"dbSNP","start":140491213,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140491213,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140491219,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491219,"source":"dbSNP","seq_region_name":"7","id":"rs1374842305","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491220,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140491220,"id":"rs1238415933","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1029055399","seq_region_name":"7","source":"dbSNP","start":140491223,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140491223,"alleles":["C","G"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140491231,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491231,"source":"dbSNP","seq_region_name":"7","id":"rs888880822","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491235,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140491235,"clinical_significance":[],"seq_region_name":"7","id":"rs1795397309"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130407521","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140491239,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491239},{"id":"rs1795397326","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140491247,"strand":1,"feature_type":"variation","start":140491247,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140491248,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491248,"source":"dbSNP","seq_region_name":"7","id":"rs1795397339","clinical_significance":[]},{"seq_region_name":"7","id":"rs1000537554","clinical_significance":[],"end":140491253,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140491253,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs184024210","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491254,"feature_type":"variation","strand":1,"end":140491254,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1032138892","source":"dbSNP","start":140491261,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140491261,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs2363817","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140491262,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491262},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130407543","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491262,"feature_type":"variation","strand":1,"alleles":["C","-"],"end":140491262},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491264,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140491264,"clinical_significance":[],"id":"rs1795397487","seq_region_name":"7"},{"end":140491266,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140491266,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795397502","seq_region_name":"7"},{"alleles":["G","A"],"end":140491267,"feature_type":"variation","strand":1,"source":"dbSNP","start":140491267,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs534202575"},{"end":140491275,"alleles":["AATTAA","AA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140491270,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1216477088","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795397563","clinical_significance":[],"end":140491276,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140491276,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140491277,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140491277,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1024878454"},{"start":140491278,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140491278,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs1293684134","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs998114032","clinical_significance":[],"end":140491279,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140491279,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1366583979","alleles":["C","G","T"],"end":140491283,"feature_type":"variation","strand":1,"source":"dbSNP","start":140491283,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["G","A"],"end":140491288,"feature_type":"variation","strand":1,"source":"dbSNP","start":140491288,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795397676"},{"end":140491291,"alleles":["G","A","C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140491291,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1029561388"},{"source":"dbSNP","start":140491299,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140491299,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs926587891"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140491301,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491301,"clinical_significance":[],"seq_region_name":"7","id":"rs953924387"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795397742","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140491302,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491302},{"seq_region_name":"7","id":"rs1795397760","clinical_significance":[],"start":140491304,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140491304,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140491305,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491305,"source":"dbSNP","seq_region_name":"7","id":"rs1795397776","clinical_significance":[]},{"source":"dbSNP","start":140491315,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140491315,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795397792","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1398806545","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140491318,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491318},{"feature_type":"variation","strand":1,"end":140491319,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491319,"clinical_significance":[],"seq_region_name":"7","id":"rs1331786039"},{"seq_region_name":"7","id":"rs1795397839","clinical_significance":[],"start":140491323,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140491323,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"alleles":["G","A"],"end":140491325,"strand":1,"feature_type":"variation","start":140491325,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795397858","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140491333,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491333,"source":"dbSNP","seq_region_name":"7","id":"rs1401373798","clinical_significance":[]},{"end":140491334,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140491334,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795397900"},{"clinical_significance":[],"seq_region_name":"7","id":"rs986159494","end":140491336,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140491336,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140491337,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140491337,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1449252033","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491338,"source":"dbSNP","strand":1,"feature_type":"variation","end":140491338,"alleles":["T","C"],"seq_region_name":"7","id":"rs1795398153","clinical_significance":[]},{"id":"rs910540945","seq_region_name":"7","clinical_significance":[],"start":140491344,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140491344,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795398182","source":"dbSNP","start":140491350,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140491350,"alleles":["G","A"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140491353,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140491353,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs372389048"},{"source":"dbSNP","start":140491357,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140491357,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1474461392"},{"seq_region_name":"7","id":"rs1585516530","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140491358,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491358,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1368227984","clinical_significance":[],"start":140491360,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G","T"],"end":140491360,"strand":1,"feature_type":"variation"},{"id":"rs1329440652","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491363,"source":"dbSNP","strand":1,"feature_type":"variation","end":140491363,"alleles":["G","A"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491364,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140491364,"clinical_significance":[],"seq_region_name":"7","id":"rs1795398266"},{"start":140491367,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140491367,"alleles":["A","AA"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1421385337","clinical_significance":[]},{"source":"dbSNP","start":140491371,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140491371,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795398289"},{"id":"rs979222028","seq_region_name":"7","clinical_significance":[],"start":140491379,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140491379,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140491380,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491380,"source":"dbSNP","seq_region_name":"7","id":"rs558860425","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795398343","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491385,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140491385},{"id":"rs1196140276","seq_region_name":"7","clinical_significance":[],"start":140491388,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140491388,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs908748201","feature_type":"variation","strand":1,"end":140491389,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491389},{"id":"rs1795398389","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491395,"source":"dbSNP","strand":1,"feature_type":"variation","end":140491395,"alleles":["T","G"]},{"seq_region_name":"7","id":"rs1795398406","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140491396,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491396,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130407641","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140491403,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491403},{"clinical_significance":[],"id":"rs1795398420","seq_region_name":"7","end":140491406,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140491406,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491410,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140491410,"id":"rs1273370166","seq_region_name":"7","clinical_significance":[]},{"end":140491414,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140491414,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1228917485","clinical_significance":[]},{"alleles":["T","G"],"end":140491417,"strand":1,"feature_type":"variation","start":140491417,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs924817917","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130407664","feature_type":"variation","strand":1,"alleles":["GGG","G"],"end":140491421,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491419},{"strand":1,"feature_type":"variation","alleles":["-","CTCCC"],"end":140491419,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491420,"source":"dbSNP","seq_region_name":"7","id":"rs1734289506","clinical_significance":[]},{"start":140491420,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140491420,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs577017272","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140491421,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491421,"source":"dbSNP","seq_region_name":"7","id":"rs1585516558","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130407677","clinical_significance":[],"start":140491422,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140491421,"alleles":["-","CTCCCAA"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1233134329","clinical_significance":[],"strand":1,"feature_type":"variation","end":140491423,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491423,"source":"dbSNP"},{"start":140491424,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140491423,"alleles":["-","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795398553","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491426,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140491426,"clinical_significance":[],"id":"rs140784704","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491431,"source":"dbSNP","strand":1,"feature_type":"variation","end":140491431,"alleles":["C","T"],"id":"rs1239749462","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491432,"feature_type":"variation","strand":1,"end":140491432,"alleles":["A","G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1829765"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1717698420","end":140491433,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140491433,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140491434,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140491434,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1304960739"},{"feature_type":"variation","strand":1,"end":140491435,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491435,"clinical_significance":[],"seq_region_name":"7","id":"rs1446067988"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491438,"feature_type":"variation","strand":1,"end":140491438,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795398735"},{"clinical_significance":[],"id":"rs901445199","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491447,"feature_type":"variation","strand":1,"end":140491447,"alleles":["G","A"]},{"clinical_significance":[],"id":"rs1328224897","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491448,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140491448},{"end":140491449,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140491449,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs2130407714","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491454,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140491454,"clinical_significance":[],"seq_region_name":"7","id":"rs1829766"},{"end":140491455,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140491455,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795398887"},{"clinical_significance":[],"id":"rs1795398919","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491467,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140491467},{"alleles":["A","G"],"end":140491471,"feature_type":"variation","strand":1,"source":"dbSNP","start":140491471,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs917530295"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795398965","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491472,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140491472},{"clinical_significance":[],"seq_region_name":"7","id":"rs1050106080","source":"dbSNP","start":140491473,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140491473,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs888743645","clinical_significance":[],"strand":1,"feature_type":"variation","end":140491478,"alleles":["T","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491478,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140491483,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491483,"clinical_significance":[],"seq_region_name":"7","id":"rs1795399061"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1231902706","source":"dbSNP","start":140491483,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["CCCCC","CCCCCC"],"end":140491487,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491484,"feature_type":"variation","strand":1,"end":140491484,"alleles":["C","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130407744"},{"alleles":["C","T"],"end":140491486,"feature_type":"variation","strand":1,"source":"dbSNP","start":140491486,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1455811466"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585516594","end":140491487,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140491487,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1829767","source":"dbSNP","start":140491488,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140491488,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1183030180","source":"dbSNP","start":140491495,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140491495,"alleles":["C","T"],"feature_type":"variation","strand":1},{"end":140491496,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140491496,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795399269","seq_region_name":"7","clinical_significance":[]},{"id":"rs763471850","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491503,"source":"dbSNP","strand":1,"feature_type":"variation","end":140491503,"alleles":["A","T"]},{"clinical_significance":[],"id":"rs1176262746","seq_region_name":"7","source":"dbSNP","start":140491515,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140491515,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140491521,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491521,"source":"dbSNP","seq_region_name":"7","id":"rs1044077649","clinical_significance":[]},{"alleles":["TT","T"],"end":140491524,"feature_type":"variation","strand":1,"source":"dbSNP","start":140491523,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1253046587"},{"clinical_significance":[],"id":"rs892330413","seq_region_name":"7","end":140491525,"alleles":["G","C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140491525,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs2130407775","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140491527,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491527,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1009383206","clinical_significance":[],"alleles":["C","A","T"],"end":140491529,"strand":1,"feature_type":"variation","start":140491529,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs2130407779","clinical_significance":[],"alleles":["A","G"],"end":140491531,"strand":1,"feature_type":"variation","start":140491531,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1025204601","clinical_significance":[],"strand":1,"feature_type":"variation","end":140491536,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491536,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1288891232","seq_region_name":"7","feature_type":"variation","strand":1,"end":140491538,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491538},{"alleles":["C","A","T"],"end":140491544,"feature_type":"variation","strand":1,"source":"dbSNP","start":140491544,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs551710792"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491545,"source":"dbSNP","strand":1,"feature_type":"variation","end":140491545,"alleles":["C","T"],"seq_region_name":"7","id":"rs1795400044","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585516618","clinical_significance":[],"strand":1,"feature_type":"variation","end":140491546,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491546,"source":"dbSNP"},{"seq_region_name":"7","id":"rs970683038","clinical_significance":[],"end":140491549,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140491549,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs888068993","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140491555,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491555,"source":"dbSNP"},{"alleles":["G","A","C","T"],"end":140491558,"strand":1,"feature_type":"variation","start":140491558,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1033680263","clinical_significance":[]},{"alleles":["A","C"],"end":140491559,"strand":1,"feature_type":"variation","start":140491559,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130407810","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795400150","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491565,"source":"dbSNP","strand":1,"feature_type":"variation","end":140491565,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795400169","source":"dbSNP","start":140491570,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140491570,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795400188","clinical_significance":[],"strand":1,"feature_type":"variation","end":140491571,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491571,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795400210","clinical_significance":[],"start":140491572,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140491572,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140491574,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491574,"source":"dbSNP","id":"rs866135881","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491580,"source":"dbSNP","strand":1,"feature_type":"variation","end":140491580,"alleles":["C","T"],"seq_region_name":"7","id":"rs138589047","clinical_significance":[]},{"end":140491582,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140491582,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs952685477","clinical_significance":[]},{"seq_region_name":"7","id":"rs570111525","clinical_significance":[],"alleles":["A","C"],"end":140491584,"strand":1,"feature_type":"variation","start":140491584,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140491586,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140491586,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795400327","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795400343","alleles":["A","G"],"end":140491587,"feature_type":"variation","strand":1,"source":"dbSNP","start":140491587,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["G","A"],"end":140491588,"feature_type":"variation","strand":1,"source":"dbSNP","start":140491588,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1330676572"},{"alleles":["G","A"],"end":140491589,"strand":1,"feature_type":"variation","start":140491589,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1319429509","clinical_significance":[]},{"start":140491592,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140491592,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs528127604","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130407846","clinical_significance":[],"end":140491596,"alleles":["-","TGTGGTGAGCTGTGAGCATG"],"strand":1,"feature_type":"variation","start":140491597,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs2130407850","clinical_significance":[],"strand":1,"feature_type":"variation","end":140491599,"alleles":["A","ATTGCAGTCAAGCCTGAGTGACAGGGCAAGACCCTGTCTCAAAAAAAAA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491599,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491604,"source":"dbSNP","strand":1,"feature_type":"variation","end":140491603,"alleles":["-","GGATCTGTGAGTCTATACCAATAATACCAATAT"],"seq_region_name":"7","id":"rs2130407852","clinical_significance":[]},{"seq_region_name":"7","id":"rs1171187730","clinical_significance":[],"start":140491610,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140491610,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491612,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140491612,"clinical_significance":[],"id":"rs1383229818","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1158612548","source":"dbSNP","start":140491620,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140491620,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795400459","clinical_significance":[],"strand":1,"feature_type":"variation","end":140491626,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491626,"source":"dbSNP"},{"clinical_significance":[],"id":"rs984237213","seq_region_name":"7","alleles":["C","T"],"end":140491630,"feature_type":"variation","strand":1,"source":"dbSNP","start":140491630,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1037158322","source":"dbSNP","start":140491632,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140491632,"alleles":["A","G"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491634,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140491634,"clinical_significance":[],"id":"rs1585516642","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795400535","clinical_significance":[],"start":140491637,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140491637,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs897003501","end":140491644,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140491644,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs998041861","seq_region_name":"7","clinical_significance":[],"start":140491647,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140491647,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"end":140491648,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140491648,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs369349680","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140491649,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491649,"source":"dbSNP","seq_region_name":"7","id":"rs1174909287","clinical_significance":[]},{"alleles":["G","A","C"],"end":140491655,"strand":1,"feature_type":"variation","start":140491655,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1029489266","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491659,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140491659,"id":"rs1245727521","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","G"],"end":140491670,"strand":1,"feature_type":"variation","start":140491670,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585516659","clinical_significance":[]},{"source":"dbSNP","start":140491673,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140491673,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1193430613","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795400679","clinical_significance":[],"start":140491678,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140491678,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"alleles":["C","T"],"end":140491680,"feature_type":"variation","strand":1,"source":"dbSNP","start":140491680,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795400693"},{"strand":1,"feature_type":"variation","end":140491681,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491681,"source":"dbSNP","seq_region_name":"7","id":"rs1448562576","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795400722","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491682,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140491682},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795400743","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140491684,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491684},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491686,"feature_type":"variation","strand":1,"end":140491686,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs961431902"},{"alleles":["T","A"],"end":140491694,"feature_type":"variation","strand":1,"source":"dbSNP","start":140491694,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1354100794"},{"start":140491698,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140491698,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs953982837","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491699,"source":"dbSNP","strand":1,"feature_type":"variation","end":140491699,"alleles":["G","C"],"seq_region_name":"7","id":"rs1795400825","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491700,"source":"dbSNP","strand":1,"feature_type":"variation","end":140491700,"alleles":["T","G"],"seq_region_name":"7","id":"rs1585516663","clinical_significance":[]},{"end":140491702,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140491702,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs540525406","clinical_significance":[]},{"clinical_significance":[],"id":"rs1448859953","seq_region_name":"7","feature_type":"variation","strand":1,"end":140491705,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491705},{"clinical_significance":[],"seq_region_name":"7","id":"rs1423565970","alleles":["C","T"],"end":140491714,"feature_type":"variation","strand":1,"source":"dbSNP","start":140491714,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491716,"feature_type":"variation","strand":1,"end":140491716,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795400919"},{"source":"dbSNP","start":140491721,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140491721,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795400945","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491722,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140491722,"clinical_significance":[],"seq_region_name":"7","id":"rs1795400963"},{"feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140491723,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491723,"clinical_significance":[],"seq_region_name":"7","id":"rs2363816"},{"clinical_significance":[],"seq_region_name":"7","id":"rs922730151","alleles":["C","T"],"end":140491724,"feature_type":"variation","strand":1,"source":"dbSNP","start":140491724,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1563104359","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140491725,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491725,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491726,"feature_type":"variation","strand":1,"end":140491726,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1271038925"},{"feature_type":"variation","strand":1,"end":140491729,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491729,"clinical_significance":[],"seq_region_name":"7","id":"rs553368175"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1279341315","feature_type":"variation","strand":1,"end":140491730,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491730},{"id":"rs1795401183","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491730,"source":"dbSNP","strand":1,"feature_type":"variation","end":140491730,"alleles":["A","-"]},{"start":140491734,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140491734,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585516689","clinical_significance":[]},{"start":140491742,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140491742,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs532310490","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491743,"feature_type":"variation","strand":1,"end":140491743,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795401233"},{"seq_region_name":"7","id":"rs1795401247","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140491744,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491744,"source":"dbSNP"},{"end":140491747,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140491747,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1338992090"},{"seq_region_name":"7","id":"rs1563104371","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140491751,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491751,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795401310","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140491754,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491754,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1297954905","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491757,"feature_type":"variation","strand":1,"end":140491760,"alleles":["TATC","TATCTATC"]},{"source":"dbSNP","start":140491760,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140491760,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1017613929","seq_region_name":"7"},{"start":140491761,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140491761,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs57745995","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795401403","source":"dbSNP","start":140491761,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140491764,"alleles":["GCCA","GCCAGCCA"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1217119393","seq_region_name":"7","feature_type":"variation","strand":1,"end":140491764,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491764},{"start":140491765,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140491765,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795401444","clinical_significance":[]},{"id":"rs932921382","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140491769,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491769,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491770,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140491770,"clinical_significance":[],"seq_region_name":"7","id":"rs1050427932"},{"clinical_significance":[],"seq_region_name":"7","id":"rs187199685","source":"dbSNP","start":140491771,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140491771,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1168208404","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140491772,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491772},{"clinical_significance":[],"id":"rs1795401539","seq_region_name":"7","source":"dbSNP","start":140491773,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140491773,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs978888852","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140491774,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491774,"source":"dbSNP"},{"id":"rs1795401570","seq_region_name":"7","clinical_significance":[],"end":140491787,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140491787,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1476182711","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491788,"source":"dbSNP","strand":1,"feature_type":"variation","end":140491788,"alleles":["A","G"]},{"start":140491790,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140491790,"alleles":["A","G"],"strand":1,"feature_type":"variation","id":"rs1312404975","seq_region_name":"7","clinical_significance":[]},{"start":140491794,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140491794,"alleles":["A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795401623","clinical_significance":[]},{"end":140491803,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140491803,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795401639","seq_region_name":"7"},{"start":140491806,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140491806,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130408035","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1192588748","alleles":["C","G"],"end":140491807,"feature_type":"variation","strand":1,"source":"dbSNP","start":140491807,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795401674","source":"dbSNP","start":140491808,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140491808,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795401694","clinical_significance":[],"start":140491813,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140491813,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491817,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140491817,"clinical_significance":[],"seq_region_name":"7","id":"rs1795401732"},{"end":140491821,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140491821,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130408044"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140491823,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491823,"clinical_significance":[],"seq_region_name":"7","id":"rs1211690367"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1032198662","end":140491827,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140491827,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140491828,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140491828,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1253719238"},{"id":"rs1795401811","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140491834,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491834,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs4726832","feature_type":"variation","strand":1,"end":140491836,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491836},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491842,"feature_type":"variation","strand":1,"end":140491842,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795401908"},{"feature_type":"variation","strand":1,"end":140491843,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491843,"clinical_significance":[],"id":"rs1053491130","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140491847,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491847,"source":"dbSNP","seq_region_name":"7","id":"rs2130408083","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795401952","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491848,"source":"dbSNP","strand":1,"feature_type":"variation","end":140491848,"alleles":["A","G"]},{"end":140491849,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140491849,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs767186747","clinical_significance":[]},{"seq_region_name":"7","id":"rs992993522","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140491851,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491851,"source":"dbSNP"},{"clinical_significance":[],"id":"rs892233782","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491857,"feature_type":"variation","strand":1,"alleles":["TATTTATTTATTTATTT","TATTTATTTATTT"],"end":140491873},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795402034","source":"dbSNP","start":140491860,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140491860,"feature_type":"variation","strand":1},{"alleles":["T","C"],"end":140491861,"strand":1,"feature_type":"variation","start":140491861,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1273795726","clinical_significance":[]},{"seq_region_name":"7","id":"rs1216602833","clinical_significance":[],"alleles":["T","C"],"end":140491867,"strand":1,"feature_type":"variation","start":140491867,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491870,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140491870,"seq_region_name":"7","id":"rs548425010","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795402109","source":"dbSNP","start":140491871,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140491871,"feature_type":"variation","strand":1},{"start":140491874,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140491874,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs948973434","clinical_significance":[]},{"seq_region_name":"7","id":"rs1234239858","clinical_significance":[],"end":140491882,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140491882,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795402161","clinical_significance":[],"start":140491888,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140491888,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1357938491","clinical_significance":[],"strand":1,"feature_type":"variation","end":140491890,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491890,"source":"dbSNP"},{"source":"dbSNP","start":140491891,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140491891,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795402196"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491891,"source":"dbSNP","strand":1,"feature_type":"variation","end":140491894,"alleles":["CTCT","CT"],"seq_region_name":"7","id":"rs1185654233","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130408124","clinical_significance":[],"strand":1,"feature_type":"variation","end":140491892,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491892,"source":"dbSNP"},{"start":140491893,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140491893,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795402236","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795402253","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491894,"source":"dbSNP","strand":1,"feature_type":"variation","end":140491894,"alleles":["T","A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs140395014","source":"dbSNP","start":140491907,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140491907,"alleles":["G","A"],"feature_type":"variation","strand":1},{"end":140491913,"alleles":["GGAGTGC","GGAGTGCCGGAGTGC"],"strand":1,"feature_type":"variation","start":140491907,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1447940581","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795402324","clinical_significance":[],"start":140491911,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140491911,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1328879751","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491914,"source":"dbSNP","strand":1,"feature_type":"variation","end":140491914,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs1415246699","clinical_significance":[],"strand":1,"feature_type":"variation","end":140491915,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491915,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1466870384","feature_type":"variation","strand":1,"end":140491921,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491921},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140491922,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491922,"clinical_significance":[],"seq_region_name":"7","id":"rs909562310"},{"clinical_significance":[],"seq_region_name":"7","id":"rs750268107","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491924,"feature_type":"variation","strand":1,"end":140491924,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs940999837","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491927,"feature_type":"variation","strand":1,"end":140491927,"alleles":["C","T"]},{"id":"rs533975198","seq_region_name":"7","clinical_significance":[],"start":140491928,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140491928,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"alleles":["G","T"],"end":140491929,"feature_type":"variation","strand":1,"source":"dbSNP","start":140491929,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1180110162"},{"source":"dbSNP","start":140491933,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140491933,"alleles":["A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795402737"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1472416479","source":"dbSNP","start":140491934,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140491934,"alleles":["C","A","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795402792","source":"dbSNP","start":140491939,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140491939,"alleles":["A","G"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491940,"feature_type":"variation","strand":1,"end":140491940,"alleles":["T","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585516750"},{"seq_region_name":"7","id":"rs1795402834","clinical_significance":[],"alleles":["T","C"],"end":140491942,"strand":1,"feature_type":"variation","start":140491942,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs6464787","clinical_significance":[],"alleles":["C","T"],"end":140491944,"strand":1,"feature_type":"variation","start":140491944,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140491945,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491945,"source":"dbSNP","seq_region_name":"7","id":"rs933720115","clinical_significance":[]},{"end":140491949,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140491949,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585516754"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585516755","end":140491955,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140491955,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1050919283","clinical_significance":[],"end":140491959,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140491959,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1456635140","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140491960,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491960,"source":"dbSNP"},{"seq_region_name":"7","id":"rs6464788","clinical_significance":[],"end":140491961,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140491961,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1005576377","seq_region_name":"7","feature_type":"variation","strand":1,"end":140491962,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491962},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795403240","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491963,"feature_type":"variation","strand":1,"end":140491963,"alleles":["A","T"]},{"end":140491966,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140491966,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1337493153","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140491968,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491968,"source":"dbSNP","seq_region_name":"7","id":"rs1015576338","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1006826613","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491969,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140491969},{"strand":1,"feature_type":"variation","end":140491971,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491971,"source":"dbSNP","seq_region_name":"7","id":"rs1022611919","clinical_significance":[]},{"end":140491972,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140491972,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs112160300","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140491979,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491979,"source":"dbSNP","id":"rs1448293791","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1373990078","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140491980,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491980},{"clinical_significance":[],"id":"rs1795403520","seq_region_name":"7","alleles":["T","C"],"end":140491983,"feature_type":"variation","strand":1,"source":"dbSNP","start":140491983,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795403543","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140491985,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491985,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491987,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140491987,"seq_region_name":"7","id":"rs556691256","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491987,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","-"],"end":140491987,"seq_region_name":"7","id":"rs1220574053","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491989,"feature_type":"variation","strand":1,"end":140491989,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1031666576"},{"id":"rs926191114","seq_region_name":"7","clinical_significance":[],"start":140491990,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140491990,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140491992,"feature_type":"variation","strand":1,"end":140491992,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795403707"},{"strand":1,"feature_type":"variation","alleles":["GGG","GGGGG"],"end":140491994,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491992,"source":"dbSNP","seq_region_name":"7","id":"rs1162358153","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140491993,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140491993,"source":"dbSNP","seq_region_name":"7","id":"rs1404695928","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1408573801","source":"dbSNP","start":140492002,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140492002,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1180610835","feature_type":"variation","strand":1,"end":140492004,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492004},{"seq_region_name":"7","id":"rs534354790","clinical_significance":[],"alleles":["C","A","T"],"end":140492007,"strand":1,"feature_type":"variation","start":140492007,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1237607244","seq_region_name":"7","alleles":["C","A","T"],"end":140492013,"feature_type":"variation","strand":1,"source":"dbSNP","start":140492013,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795403985","end":140492022,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140492022,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs992836315","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492024,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140492024},{"seq_region_name":"7","id":"rs1264054780","clinical_significance":[],"alleles":["T","C"],"end":140492026,"strand":1,"feature_type":"variation","start":140492026,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140492026,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140492032,"alleles":["TTTTTTT","TTTTTTTT"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs936232846"},{"id":"rs1221251233","seq_region_name":"7","clinical_significance":[],"alleles":["T","G"],"end":140492028,"strand":1,"feature_type":"variation","start":140492028,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs766781763","alleles":["T","C"],"end":140492030,"feature_type":"variation","strand":1,"source":"dbSNP","start":140492030,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492033,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140492033,"id":"rs2130408302","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1053396422","feature_type":"variation","strand":1,"end":140492035,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492035},{"source":"dbSNP","start":140492041,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140492041,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1214886541"},{"source":"dbSNP","start":140492044,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140492044,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795404190","seq_region_name":"7"},{"start":140492045,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140492045,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1024437858","clinical_significance":[]},{"seq_region_name":"7","id":"rs1238575006","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492047,"source":"dbSNP","strand":1,"feature_type":"variation","end":140492047,"alleles":["G","A"]},{"source":"dbSNP","start":140492049,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140492049,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795404267"},{"source":"dbSNP","start":140492052,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140492052,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1374099388"},{"alleles":["C","T"],"end":140492057,"feature_type":"variation","strand":1,"source":"dbSNP","start":140492057,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795404313"},{"id":"rs2130408323","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492058,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140492058},{"seq_region_name":"7","id":"rs536330600","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140492059,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492059,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1478861564","clinical_significance":[],"start":140492060,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140492060,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1441192680","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140492063,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492063},{"id":"rs945148048","seq_region_name":"7","clinical_significance":[],"alleles":["G","A","T"],"end":140492066,"strand":1,"feature_type":"variation","start":140492066,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140492067,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492067,"clinical_significance":[],"seq_region_name":"7","id":"rs2130408346"},{"seq_region_name":"7","id":"rs554745796","clinical_significance":[],"start":140492069,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","G"],"end":140492069,"strand":1,"feature_type":"variation"},{"alleles":["A","G"],"end":140492070,"strand":1,"feature_type":"variation","start":140492070,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs572874690","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140492071,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492071,"clinical_significance":[],"id":"rs1795404524","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1160423434","clinical_significance":[],"start":140492073,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140492073,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492075,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140492075,"seq_region_name":"7","id":"rs1054943191","clinical_significance":[]},{"clinical_significance":[],"id":"rs1379782112","seq_region_name":"7","alleles":["G","C","T"],"end":140492076,"feature_type":"variation","strand":1,"source":"dbSNP","start":140492076,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140492080,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140492080,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs1174269461","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140492081,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492081,"source":"dbSNP","id":"rs1435162446","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795404692","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492082,"source":"dbSNP","strand":1,"feature_type":"variation","end":140492082,"alleles":["A","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1159317569","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492088,"feature_type":"variation","strand":1,"end":140492088,"alleles":["T","A"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492089,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140492089,"seq_region_name":"7","id":"rs1363081938","clinical_significance":[]},{"clinical_significance":[],"id":"rs1190811278","seq_region_name":"7","feature_type":"variation","strand":1,"end":140492094,"alleles":["C","A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492094},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585516819","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492099,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140492099},{"alleles":["CCGCC","CCGCCGCC"],"end":140492104,"feature_type":"variation","strand":1,"source":"dbSNP","start":140492100,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795404800","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs540190636","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492101,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140492101},{"feature_type":"variation","strand":1,"end":140492102,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492102,"clinical_significance":[],"seq_region_name":"7","id":"rs1244191972"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492104,"source":"dbSNP","strand":1,"feature_type":"variation","end":140492104,"alleles":["C","T"],"seq_region_name":"7","id":"rs1795404882","clinical_significance":[]},{"seq_region_name":"7","id":"rs941609248","clinical_significance":[],"alleles":["C","A","T"],"end":140492105,"strand":1,"feature_type":"variation","start":140492105,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs575802268","seq_region_name":"7","clinical_significance":[],"end":140492106,"alleles":["G","A","C","T"],"strand":1,"feature_type":"variation","start":140492106,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs764146821","source":"dbSNP","start":140492110,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140492110,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs918217032","end":140492111,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140492111,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs577038870","clinical_significance":[],"start":140492113,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140492113,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"id":"rs1795405034","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492118,"source":"dbSNP","strand":1,"feature_type":"variation","end":140492118,"alleles":["C","G"]},{"clinical_significance":[],"id":"rs1585516845","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492119,"feature_type":"variation","strand":1,"end":140492119,"alleles":["A","C","G"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492124,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140492124,"clinical_significance":[],"seq_region_name":"7","id":"rs1050802727"},{"clinical_significance":[],"seq_region_name":"7","id":"rs544207366","end":140492127,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140492127,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs942550646","end":140492129,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140492129,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1030148293","clinical_significance":[],"start":140492130,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140492130,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140492131,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140492131,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs4725710"},{"alleles":["G","A"],"end":140492136,"strand":1,"feature_type":"variation","start":140492136,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795405256","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492141,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140492141,"clinical_significance":[],"seq_region_name":"7","id":"rs1223175568"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140492143,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492143,"source":"dbSNP","seq_region_name":"7","id":"rs1795405306","clinical_significance":[]},{"alleles":["C","T"],"end":140492144,"strand":1,"feature_type":"variation","start":140492144,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795405322","clinical_significance":[]},{"seq_region_name":"7","id":"rs1313587603","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492145,"source":"dbSNP","strand":1,"feature_type":"variation","end":140492145,"alleles":["C","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1290460003","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140492146,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492146},{"seq_region_name":"7","id":"rs1795405364","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492147,"source":"dbSNP","strand":1,"feature_type":"variation","end":140492289,"alleles":["CCGCACCCGGCCATTCTGGACTATTTCTGTGTCCACTTGTGGCTGAGTATAGCAACCATACAATAAAACCCCTCTTCCACTGTCTTAGCTGAAGAACTAAAAAAAAAAAAAAAAAAAAATGAGTGGTGCATGCCTGTAGTCCC","CC"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563104476","feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140492148,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492148},{"seq_region_name":"7","id":"rs185464259","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492149,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140492149},{"strand":1,"feature_type":"variation","end":140492151,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492151,"source":"dbSNP","seq_region_name":"7","id":"rs1375971024","clinical_significance":[]},{"source":"dbSNP","start":140492153,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140492153,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1219041432"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1251434257","source":"dbSNP","start":140492154,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140492154,"alleles":["C","T"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492155,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140492155,"clinical_significance":[],"seq_region_name":"7","id":"rs1468202384"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1179382717","end":140492156,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140492156,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795405544","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492158,"source":"dbSNP","strand":1,"feature_type":"variation","end":140492158,"alleles":["C","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492160,"source":"dbSNP","strand":1,"feature_type":"variation","end":140492160,"alleles":["T","G"],"seq_region_name":"7","id":"rs1795405573","clinical_significance":[]},{"seq_region_name":"7","id":"rs999444022","clinical_significance":[],"end":140492163,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140492163,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140492165,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140492165,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130408501","clinical_significance":[]},{"seq_region_name":"7","id":"rs548273178","clinical_significance":[],"start":140492171,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140492171,"strand":1,"feature_type":"variation"},{"id":"rs1795405635","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140492173,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492173,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492177,"source":"dbSNP","strand":1,"feature_type":"variation","end":140492177,"alleles":["G","A","T"],"seq_region_name":"7","id":"rs957625075","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492180,"feature_type":"variation","strand":1,"end":140492180,"alleles":["C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1563104486"},{"clinical_significance":[],"id":"rs1795405700","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492183,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140492183},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140492185,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492185,"clinical_significance":[],"seq_region_name":"7","id":"rs988983580"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492186,"source":"dbSNP","strand":1,"feature_type":"variation","end":140492186,"alleles":["T","A"],"id":"rs1795405740","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795405757","source":"dbSNP","start":140492191,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140492191,"alleles":["G","C"],"feature_type":"variation","strand":1},{"id":"rs1795405771","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492192,"source":"dbSNP","strand":1,"feature_type":"variation","end":140492192,"alleles":["A","C"]},{"source":"dbSNP","start":140492193,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140492193,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs560166220"},{"start":140492195,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140492195,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs527787492","clinical_significance":[]},{"source":"dbSNP","start":140492196,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140492196,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs2130408541","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140492197,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492197,"source":"dbSNP","seq_region_name":"7","id":"rs1232095157","clinical_significance":[]},{"start":140492202,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140492202,"strand":1,"feature_type":"variation","id":"rs1307651949","seq_region_name":"7","clinical_significance":[]},{"start":140492205,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140492205,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130408549","clinical_significance":[]},{"id":"rs2130408551","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140492210,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492210,"source":"dbSNP"},{"end":140492216,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140492216,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130408553","clinical_significance":[]},{"source":"dbSNP","start":140492225,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C","T"],"end":140492225,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585516883"},{"clinical_significance":[],"seq_region_name":"7","id":"rs981911619","feature_type":"variation","strand":1,"end":140492229,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492229},{"clinical_significance":[],"seq_region_name":"7","id":"rs927683992","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492230,"feature_type":"variation","strand":1,"alleles":["C","A","G"],"end":140492230},{"seq_region_name":"7","id":"rs1293879793","clinical_significance":[],"alleles":["T","C"],"end":140492232,"strand":1,"feature_type":"variation","start":140492232,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795405957","clinical_significance":[],"start":140492234,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140492234,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1163204765","source":"dbSNP","start":140492236,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A","G"],"end":140492236,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140492240,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492240,"source":"dbSNP","seq_region_name":"7","id":"rs1447018732","clinical_significance":[]},{"alleles":["ACTA","A"],"end":140492245,"strand":1,"feature_type":"variation","start":140492242,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1332845205","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795406042","feature_type":"variation","strand":1,"alleles":["C","A","G"],"end":140492243,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492243},{"seq_region_name":"7","id":"rs1795406067","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492243,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","-"],"end":140492243},{"seq_region_name":"7","id":"rs1333515709","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492243,"source":"dbSNP","strand":1,"feature_type":"variation","end":140492244,"alleles":["CT","-"]},{"start":140492244,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A","C"],"end":140492244,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1462689834","clinical_significance":[]},{"end":140492244,"alleles":["T","-"],"strand":1,"feature_type":"variation","start":140492244,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1674620045","clinical_significance":[]},{"start":140492244,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TA","-"],"end":140492245,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1563104497","clinical_significance":[]},{"source":"dbSNP","start":140492244,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TAA","-"],"end":140492246,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs755117101"},{"alleles":["TAAA","-"],"end":140492247,"feature_type":"variation","strand":1,"source":"dbSNP","start":140492244,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs759229543"},{"alleles":["A","G","T"],"end":140492245,"strand":1,"feature_type":"variation","start":140492245,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1457952513","clinical_significance":[]},{"source":"dbSNP","start":140492245,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAA","AAAAAAAAAAAAA","AAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA"],"end":140492265,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs561156827"},{"end":140492246,"alleles":["A","C","G","T"],"strand":1,"feature_type":"variation","start":140492246,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1440752930","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492247,"feature_type":"variation","strand":1,"alleles":["A","C","T"],"end":140492247,"clinical_significance":[],"id":"rs1284725776","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140492248,"alleles":["A","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492248,"source":"dbSNP","seq_region_name":"7","id":"rs1358366897","clinical_significance":[]},{"alleles":["A","G"],"end":140492250,"strand":1,"feature_type":"variation","start":140492250,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1265799751","seq_region_name":"7","clinical_significance":[]},{"end":140492251,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140492251,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795406572","clinical_significance":[]},{"alleles":["A","G"],"end":140492259,"strand":1,"feature_type":"variation","start":140492259,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795406591","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795406610","clinical_significance":[],"start":140492261,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["-","G"],"end":140492260,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795406632","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492261,"feature_type":"variation","strand":1,"end":140492261,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs1795406664","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["AAAAAT","-"],"end":140492266,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492261,"source":"dbSNP"},{"start":140492262,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140492262,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1272279049","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs201024388","feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140492264,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492264},{"strand":1,"feature_type":"variation","end":140492266,"alleles":["AAT","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492264,"source":"dbSNP","seq_region_name":"7","id":"rs1334502264","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["-","G"],"end":140492264,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492265,"source":"dbSNP","seq_region_name":"7","id":"rs1563104510","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795406863","clinical_significance":[],"strand":1,"feature_type":"variation","end":140492265,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492265,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795406875","alleles":["A","AAAAAGA"],"end":140492265,"feature_type":"variation","strand":1,"source":"dbSNP","start":140492265,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563104512","feature_type":"variation","strand":1,"alleles":["AT","-"],"end":140492266,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492265},{"seq_region_name":"7","id":"rs79397509","clinical_significance":[],"end":140492266,"alleles":["T","A","G"],"strand":1,"feature_type":"variation","start":140492266,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1199532154","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492266,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","-"],"end":140492266},{"clinical_significance":[],"seq_region_name":"7","id":"rs1436155927","source":"dbSNP","start":140492268,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140492268,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492269,"feature_type":"variation","strand":1,"end":140492269,"alleles":["G","C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1379177677"},{"feature_type":"variation","strand":1,"end":140492270,"alleles":["T","A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492270,"clinical_significance":[],"seq_region_name":"7","id":"rs1035645485"},{"strand":1,"feature_type":"variation","end":140492272,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492272,"source":"dbSNP","seq_region_name":"7","id":"rs1795407138","clinical_significance":[]},{"alleles":["T","C","G"],"end":140492273,"strand":1,"feature_type":"variation","start":140492273,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1238613674","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1474055294","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492274,"feature_type":"variation","strand":1,"end":140492274,"alleles":["G","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1163270833","feature_type":"variation","strand":1,"alleles":["T","A","C","G"],"end":140492277,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492277},{"alleles":["C","T"],"end":140492280,"strand":1,"feature_type":"variation","start":140492280,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1395747286","clinical_significance":[]},{"clinical_significance":[],"id":"rs1054974730","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492284,"feature_type":"variation","strand":1,"end":140492284,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs888244462","source":"dbSNP","start":140492293,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140492293,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795407363","clinical_significance":[],"alleles":["A","G"],"end":140492294,"strand":1,"feature_type":"variation","start":140492294,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492296,"feature_type":"variation","strand":1,"end":140492296,"alleles":["T","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795407392"},{"seq_region_name":"7","id":"rs570780198","clinical_significance":[],"start":140492297,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140492297,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140492302,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492302,"source":"dbSNP","seq_region_name":"7","id":"rs941299998","clinical_significance":[]},{"seq_region_name":"7","id":"rs1024321666","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492303,"source":"dbSNP","strand":1,"feature_type":"variation","end":140492303,"alleles":["G","T"]},{"id":"rs1795407509","seq_region_name":"7","clinical_significance":[],"start":140492305,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140492305,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"id":"rs1183139856","seq_region_name":"7","clinical_significance":[],"start":140492305,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140492308,"alleles":["TGAG","TGAGTGAG"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795407531","source":"dbSNP","start":140492310,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140492310,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140492318,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492318,"clinical_significance":[],"seq_region_name":"7","id":"rs1466435698"},{"feature_type":"variation","strand":1,"end":140492319,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492319,"clinical_significance":[],"seq_region_name":"7","id":"rs1239466805"},{"start":140492320,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140492320,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs970098891","clinical_significance":[]},{"alleles":["T","C"],"end":140492322,"strand":1,"feature_type":"variation","start":140492322,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1290331913","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140492324,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492324,"source":"dbSNP","id":"rs1211368507","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1354187443","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492334,"feature_type":"variation","strand":1,"end":140492334,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs538510409","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492336,"source":"dbSNP","strand":1,"feature_type":"variation","end":140492336,"alleles":["C","G","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs111528037","source":"dbSNP","start":140492337,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140492337,"alleles":["G","A","T"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492343,"source":"dbSNP","strand":1,"feature_type":"variation","end":140492343,"alleles":["T","G"],"seq_region_name":"7","id":"rs1585516971","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140492344,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492344,"clinical_significance":[],"seq_region_name":"7","id":"rs1408924434"},{"start":140492345,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140492345,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585516975","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1446336883","feature_type":"variation","strand":1,"end":140492347,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492347},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795407966","alleles":["T","C"],"end":140492348,"feature_type":"variation","strand":1,"source":"dbSNP","start":140492348,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1795407989","seq_region_name":"7","source":"dbSNP","start":140492349,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140492349,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795408012","clinical_significance":[],"alleles":["C","G"],"end":140492352,"strand":1,"feature_type":"variation","start":140492352,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1371950344","end":140492353,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140492353,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140492357,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492357,"source":"dbSNP","seq_region_name":"7","id":"rs1325973723","clinical_significance":[]},{"seq_region_name":"7","id":"rs963329890","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492361,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","G","T"],"end":140492361},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492362,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140492362,"seq_region_name":"7","id":"rs1390431207","clinical_significance":[]},{"end":140492377,"alleles":["GCCACTGGTGCCACTG","GCCACTGGTGCCACTGGTGCCACTG"],"strand":1,"feature_type":"variation","start":140492362,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795408154","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795408177","source":"dbSNP","start":140492363,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140492363,"alleles":["C","T"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140492365,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140492365,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130408795"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795408218","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492366,"feature_type":"variation","strand":1,"end":140492366,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795408241","end":140492367,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140492367,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1159724189","seq_region_name":"7","source":"dbSNP","start":140492368,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140492368,"alleles":["G","A"],"feature_type":"variation","strand":1},{"alleles":["C","T"],"end":140492372,"feature_type":"variation","strand":1,"source":"dbSNP","start":140492372,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795408294"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1422050587","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492374,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140492374},{"clinical_significance":[],"id":"rs1342236995","seq_region_name":"7","feature_type":"variation","strand":1,"end":140492378,"alleles":["C","A","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492378},{"seq_region_name":"7","id":"rs568632988","clinical_significance":[],"start":140492379,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140492379,"alleles":["G","A","T"],"strand":1,"feature_type":"variation"},{"alleles":["G","A"],"end":140492381,"strand":1,"feature_type":"variation","start":140492381,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1246874796","clinical_significance":[]},{"source":"dbSNP","start":140492383,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140492383,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1200516857","seq_region_name":"7"},{"start":140492387,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140492387,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","id":"rs1449694318","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs535724210","source":"dbSNP","start":140492388,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140492388,"alleles":["G","A","C"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492388,"feature_type":"variation","strand":1,"end":140492392,"alleles":["GGGGG","GGGG"],"clinical_significance":[],"id":"rs1266403656","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1795409569","seq_region_name":"7","feature_type":"variation","strand":1,"end":140492389,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492389},{"seq_region_name":"7","id":"rs1284013417","clinical_significance":[],"alleles":["G","C"],"end":140492392,"strand":1,"feature_type":"variation","start":140492392,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["CAGAGCGAGATTACAGCCCCAGGGGACAGAGCGAGA","CAGAGCGAGA"],"end":140492428,"feature_type":"variation","strand":1,"source":"dbSNP","start":140492393,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1340928643","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492395,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140492395,"clinical_significance":[],"seq_region_name":"7","id":"rs1795409660"},{"seq_region_name":"7","id":"rs1795409679","clinical_significance":[],"start":140492396,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140492396,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["C","A","G","T"],"end":140492398,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492398,"source":"dbSNP","seq_region_name":"7","id":"rs564791473","clinical_significance":[]},{"clinical_significance":[],"id":"rs1239457965","seq_region_name":"7","alleles":["G","A"],"end":140492399,"feature_type":"variation","strand":1,"source":"dbSNP","start":140492399,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795409771","clinical_significance":[],"start":140492403,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140492402,"alleles":["-","C"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140492403,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140492403,"alleles":["T","A","C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs6943301"},{"source":"dbSNP","start":140492404,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140492403,"alleles":["-","ACAGCCCCAGGAGACAGAGCGAGAC"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795409790"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492405,"source":"dbSNP","strand":1,"feature_type":"variation","end":140492405,"alleles":["A","C"],"seq_region_name":"7","id":"rs1795409813","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492406,"source":"dbSNP","strand":1,"feature_type":"variation","end":140492406,"alleles":["C","T"],"id":"rs986445430","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1231335346","source":"dbSNP","start":140492408,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140492408,"alleles":["G","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795409882","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492410,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140492410},{"seq_region_name":"7","id":"rs1795409914","clinical_significance":[],"end":140492412,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140492412,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1033142395","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492413,"feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140492413},{"feature_type":"variation","strand":1,"alleles":["-","A"],"end":140492415,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492416,"clinical_significance":[],"seq_region_name":"7","id":"rs1795409966"},{"clinical_significance":[],"seq_region_name":"7","id":"rs4725711","alleles":["G","A","C","T"],"end":140492416,"feature_type":"variation","strand":1,"source":"dbSNP","start":140492416,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795410080","source":"dbSNP","start":140492417,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140492416,"alleles":["-","ACAGAGCGAGACTCCAGCCCCAGGA"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795410100","clinical_significance":[],"start":140492417,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140492417,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"alleles":["C","G"],"end":140492419,"strand":1,"feature_type":"variation","start":140492419,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs989054110","seq_region_name":"7","clinical_significance":[]},{"end":140492420,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140492420,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795410137","clinical_significance":[]},{"source":"dbSNP","start":140492420,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140492423,"alleles":["AGAG","AG"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1295831840"},{"end":140492421,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140492421,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1418613595","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492424,"source":"dbSNP","strand":1,"feature_type":"variation","end":140492424,"alleles":["C","A","G","T"],"seq_region_name":"7","id":"rs1563104555","clinical_significance":[]},{"source":"dbSNP","start":140492425,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140492425,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs942455816","seq_region_name":"7"},{"end":140492431,"alleles":["GACTC","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140492427,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1174035138"},{"source":"dbSNP","start":140492429,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140492429,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130408926"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795410279","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140492432,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492432},{"clinical_significance":[],"id":"rs1476828578","seq_region_name":"7","feature_type":"variation","strand":1,"end":140492437,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492437},{"seq_region_name":"7","id":"rs140995823","clinical_significance":[],"start":140492438,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140492438,"strand":1,"feature_type":"variation"},{"start":140492439,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140492439,"alleles":["A","ACAGA"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795410351","clinical_significance":[]},{"alleles":["AA","AAGAA"],"end":140492440,"feature_type":"variation","strand":1,"source":"dbSNP","start":140492439,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130408936"},{"end":140492446,"alleles":["AAAGAAAG","AAAGAAAGAAAG"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140492439,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs35344869"},{"feature_type":"variation","strand":1,"alleles":["AA","AAAGAA"],"end":140492441,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492440,"clinical_significance":[],"seq_region_name":"7","id":"rs141527169"},{"end":140492443,"alleles":["AGA","AGACAGA"],"strand":1,"feature_type":"variation","start":140492441,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs966424863","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["AAA","AAACAAA"],"end":140492445,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492443,"clinical_significance":[],"seq_region_name":"7","id":"rs1795410478"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795410499","feature_type":"variation","strand":1,"end":140492444,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492444},{"clinical_significance":[],"seq_region_name":"7","id":"rs1554453404","end":140492445,"alleles":["AA","AAAGAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140492444,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1486966740","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492445,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AG","AGAGAG"],"end":140492446},{"clinical_significance":[],"seq_region_name":"7","id":"rs397807313","source":"dbSNP","start":140492447,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["-","AAAT"],"end":140492446,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1257355326","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492447,"feature_type":"variation","strand":1,"end":140492447,"alleles":["T","A"]},{"seq_region_name":"7","id":"rs1043989964","clinical_significance":[],"start":140492452,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140492452,"strand":1,"feature_type":"variation"},{"end":140492455,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140492455,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1215770745","seq_region_name":"7"},{"id":"rs1795410636","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492458,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140492458},{"end":140492464,"alleles":["AAAT","-"],"strand":1,"feature_type":"variation","start":140492461,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1196287517","clinical_significance":[]},{"clinical_significance":[],"id":"rs1280815180","seq_region_name":"7","feature_type":"variation","strand":1,"end":140492472,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492472},{"id":"rs1198967600","seq_region_name":"7","clinical_significance":[],"end":140492473,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140492473,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140492475,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140492475,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795410721","clinical_significance":[]},{"seq_region_name":"7","id":"rs533895075","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492477,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140492477},{"source":"dbSNP","start":140492490,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140492490,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs937749330","seq_region_name":"7"},{"alleles":["C","-"],"end":140492490,"strand":1,"feature_type":"variation","start":140492490,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1474860225","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492491,"feature_type":"variation","strand":1,"end":140492491,"alleles":["G","A"],"clinical_significance":[],"id":"rs990568910","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492492,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140492492,"clinical_significance":[],"seq_region_name":"7","id":"rs1432280349"},{"clinical_significance":[],"id":"rs925103981","seq_region_name":"7","alleles":["C","A","G","T"],"end":140492495,"feature_type":"variation","strand":1,"source":"dbSNP","start":140492495,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140492500,"alleles":["TT","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492499,"clinical_significance":[],"seq_region_name":"7","id":"rs1795410886"},{"start":140492500,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140492500,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs935255092","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795410924","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492503,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140492503},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140492504,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492504,"clinical_significance":[],"seq_region_name":"7","id":"rs1795410946"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1052276979","alleles":["C","A","T"],"end":140492507,"feature_type":"variation","strand":1,"source":"dbSNP","start":140492507,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140492508,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140492508,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1361024799","clinical_significance":[]},{"source":"dbSNP","start":140492510,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140492510,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs4725712"},{"seq_region_name":"7","id":"rs941161040","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140492512,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492512,"source":"dbSNP"},{"seq_region_name":"7","id":"rs746044796","clinical_significance":[],"end":140492513,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140492513,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795411118","feature_type":"variation","strand":1,"end":140492519,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492519},{"seq_region_name":"7","id":"rs1795411146","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492522,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140492522},{"clinical_significance":[],"seq_region_name":"7","id":"rs1170922530","alleles":["A","G"],"end":140492525,"feature_type":"variation","strand":1,"source":"dbSNP","start":140492525,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1036974750","clinical_significance":[],"strand":1,"feature_type":"variation","end":140492526,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492526,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492538,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140492538,"clinical_significance":[],"seq_region_name":"7","id":"rs1795411221"},{"source":"dbSNP","start":140492541,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140492541,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1293168948","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492545,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140492545,"id":"rs1421203893","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1324944107","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492555,"feature_type":"variation","strand":1,"end":140492555,"alleles":["A","C"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492560,"source":"dbSNP","strand":1,"feature_type":"variation","end":140492560,"alleles":["C","T"],"id":"rs1795411383","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795411396","clinical_significance":[],"start":140492569,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140492569,"strand":1,"feature_type":"variation"},{"alleles":["T","C"],"end":140492570,"strand":1,"feature_type":"variation","start":140492570,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1014234814","clinical_significance":[]},{"start":140492573,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A","C","G"],"end":140492573,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs11766760","clinical_significance":[]},{"alleles":["T","C","G"],"end":140492576,"feature_type":"variation","strand":1,"source":"dbSNP","start":140492576,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs933893133"},{"clinical_significance":[],"id":"rs1185463539","seq_region_name":"7","alleles":["AAATAAAAAATAAAAA","AAATAAAAA"],"end":140492593,"feature_type":"variation","strand":1,"source":"dbSNP","start":140492578,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140492579,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492579,"source":"dbSNP","id":"rs1442080443","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492581,"feature_type":"variation","strand":1,"end":140492581,"alleles":["T","C"],"clinical_significance":[],"id":"rs1350155546","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1795411575","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492586,"feature_type":"variation","strand":1,"end":140492586,"alleles":["A","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492588,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140492588,"clinical_significance":[],"id":"rs1200723528","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1051542228","alleles":["A","G"],"end":140492590,"feature_type":"variation","strand":1,"source":"dbSNP","start":140492590,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795411636","clinical_significance":[],"start":140492594,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140492594,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1208752241","clinical_significance":[],"alleles":["C","T"],"end":140492596,"strand":1,"feature_type":"variation","start":140492596,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140492597,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140492597,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs4725713"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492598,"source":"dbSNP","strand":1,"feature_type":"variation","end":140492598,"alleles":["C","T"],"seq_region_name":"7","id":"rs1795411767","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492599,"source":"dbSNP","strand":1,"feature_type":"variation","end":140492599,"alleles":["C","T"],"seq_region_name":"7","id":"rs1229406071","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs562686981","end":140492600,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140492600,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795411833","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492600,"feature_type":"variation","strand":1,"alleles":["GGG","GGGG"],"end":140492602},{"seq_region_name":"7","id":"rs1795411861","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492601,"source":"dbSNP","strand":1,"feature_type":"variation","end":140492601,"alleles":["G","A"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492602,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140492602,"clinical_significance":[],"seq_region_name":"7","id":"rs574678305"},{"alleles":["CGTGGTGGCTC","C"],"end":140492613,"feature_type":"variation","strand":1,"source":"dbSNP","start":140492603,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs201311384"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492604,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C","T"],"end":140492604,"id":"rs4725714","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492605,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140492605,"clinical_significance":[],"seq_region_name":"7","id":"rs1795412010"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492607,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140492607,"seq_region_name":"7","id":"rs1381364189","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140492614,"alleles":["CTCA","CTCACTCA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492611,"source":"dbSNP","seq_region_name":"7","id":"rs1795412169","clinical_significance":[]},{"start":140492613,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140492613,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1260060694","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492614,"source":"dbSNP","strand":1,"feature_type":"variation","end":140492614,"alleles":["A","G"],"seq_region_name":"7","id":"rs1428239708","clinical_significance":[]},{"alleles":["G","A"],"end":140492616,"feature_type":"variation","strand":1,"source":"dbSNP","start":140492616,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs559933214","seq_region_name":"7"},{"end":140492620,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140492620,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1001624363"},{"source":"dbSNP","start":140492623,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140492623,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1169405928"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1452046881","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140492625,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492625},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492626,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140492626,"id":"rs1415808616","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795412328","source":"dbSNP","start":140492626,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140492634,"alleles":["CCAGCACTT","-"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1017528484","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492630,"source":"dbSNP","strand":1,"feature_type":"variation","end":140492630,"alleles":["C","G"]},{"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140492633,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492633,"clinical_significance":[],"seq_region_name":"7","id":"rs1795412368"},{"start":140492635,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140492635,"alleles":["T","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795412384","clinical_significance":[]},{"end":140492654,"alleles":["AGGCCGAGGCGGGCAG","AG"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140492639,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795412406"},{"clinical_significance":[],"seq_region_name":"7","id":"rs962882387","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140492640,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492640},{"start":140492641,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140492641,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795412439","clinical_significance":[]},{"seq_region_name":"7","id":"rs1472531103","clinical_significance":[],"strand":1,"feature_type":"variation","end":140492642,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492642,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492643,"source":"dbSNP","strand":1,"feature_type":"variation","end":140492643,"alleles":["C","A","T"],"seq_region_name":"7","id":"rs11975266","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492644,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140492644,"id":"rs769206562","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130409233","clinical_significance":[],"end":140492646,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140492646,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795412574","clinical_significance":[],"strand":1,"feature_type":"variation","end":140492648,"alleles":["C","A","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492648,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492649,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140492649,"seq_region_name":"7","id":"rs955593119","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140492658,"alleles":["CAGATCA","CAGATCAGATCA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492652,"source":"dbSNP","seq_region_name":"7","id":"rs1795412628","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492653,"source":"dbSNP","strand":1,"feature_type":"variation","end":140492653,"alleles":["A","G"],"id":"rs2130409249","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140492654,"alleles":["G","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492654,"clinical_significance":[],"id":"rs1795412651","seq_region_name":"7"},{"id":"rs1222721269","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492659,"source":"dbSNP","strand":1,"feature_type":"variation","end":140492659,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130409264","feature_type":"variation","strand":1,"end":140492659,"alleles":["-","CT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492660},{"clinical_significance":[],"seq_region_name":"7","id":"rs1323856817","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492660,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140492660},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140492662,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492662,"clinical_significance":[],"seq_region_name":"7","id":"rs371904541"},{"start":140492663,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140492663,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795412723","clinical_significance":[]},{"source":"dbSNP","start":140492666,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140492666,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs986497651"},{"seq_region_name":"7","id":"rs1228249454","clinical_significance":[],"start":140492667,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140492668,"alleles":["GG","G"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140492676,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140492676,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1358181551"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140492677,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492677,"clinical_significance":[],"seq_region_name":"7","id":"rs1795412808"},{"end":140492678,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140492678,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795412825"},{"seq_region_name":"7","id":"rs1795412845","clinical_significance":[],"alleles":["C","A"],"end":140492679,"strand":1,"feature_type":"variation","start":140492679,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140492681,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492681,"source":"dbSNP","seq_region_name":"7","id":"rs1795412865","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140492682,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492682,"source":"dbSNP","seq_region_name":"7","id":"rs1795412889","clinical_significance":[]},{"clinical_significance":[],"id":"rs910886335","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492684,"feature_type":"variation","strand":1,"end":140492684,"alleles":["T","G"]},{"seq_region_name":"7","id":"rs1795412940","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492686,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140492686},{"end":140492687,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140492687,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1448541586"},{"strand":1,"feature_type":"variation","alleles":["AA","AAA"],"end":140492690,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492689,"source":"dbSNP","id":"rs869308394","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs190359452","feature_type":"variation","strand":1,"end":140492690,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492690},{"clinical_significance":[],"seq_region_name":"7","id":"rs1554453436","feature_type":"variation","strand":1,"end":140492691,"alleles":["C","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492691},{"seq_region_name":"7","id":"rs1795412974","clinical_significance":[],"end":140492691,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140492691,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140492693,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492693,"source":"dbSNP","seq_region_name":"7","id":"rs1795413030","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1324476321","feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140492694,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492694},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492695,"feature_type":"variation","strand":1,"end":140492695,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795413069"},{"alleles":["C","T"],"end":140492701,"feature_type":"variation","strand":1,"source":"dbSNP","start":140492701,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795413090"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492701,"source":"dbSNP","strand":1,"feature_type":"variation","end":140492707,"alleles":["CCCCCTC","C"],"seq_region_name":"7","id":"rs1373456641","clinical_significance":[]},{"source":"dbSNP","start":140492702,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140492702,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795413126"},{"clinical_significance":[],"seq_region_name":"7","id":"rs564490090","alleles":["C","T"],"end":140492704,"feature_type":"variation","strand":1,"source":"dbSNP","start":140492704,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["C","A","G","T"],"end":140492705,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492705,"source":"dbSNP","seq_region_name":"7","id":"rs11765323","clinical_significance":[]},{"clinical_significance":[],"id":"rs1739717155","seq_region_name":"7","alleles":["T","A"],"end":140492706,"feature_type":"variation","strand":1,"source":"dbSNP","start":140492706,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","G","T"],"end":140492709,"feature_type":"variation","strand":1,"source":"dbSNP","start":140492709,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs867973228"},{"seq_region_name":"7","id":"rs546560862","clinical_significance":[],"start":140492712,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G","T"],"end":140492712,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140492718,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492718,"source":"dbSNP","seq_region_name":"7","id":"rs1795413312","clinical_significance":[]},{"alleles":["A","C"],"end":140492722,"feature_type":"variation","strand":1,"source":"dbSNP","start":140492722,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795413344"},{"seq_region_name":"7","id":"rs925124039","clinical_significance":[],"end":140492729,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140492729,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140492733,"alleles":["G","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492733,"clinical_significance":[],"seq_region_name":"7","id":"rs935157201"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492734,"feature_type":"variation","strand":1,"end":140492734,"alleles":["G","A"],"clinical_significance":[],"id":"rs1052203354","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs747673144","source":"dbSNP","start":140492736,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140492736,"alleles":["C","T"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492737,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140492737,"seq_region_name":"7","id":"rs1191961633","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585517200","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140492741,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492741},{"id":"rs1489710734","seq_region_name":"7","clinical_significance":[],"end":140492744,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140492744,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs949296960","clinical_significance":[],"alleles":["G","A"],"end":140492745,"strand":1,"feature_type":"variation","start":140492745,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs962432133","clinical_significance":[],"end":140492748,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140492748,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795413533","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492750,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140492750},{"seq_region_name":"7","id":"rs972992601","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492752,"source":"dbSNP","strand":1,"feature_type":"variation","end":140492752,"alleles":["T","C"]},{"alleles":["T","C"],"end":140492754,"feature_type":"variation","strand":1,"source":"dbSNP","start":140492754,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1286150967"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1241627056","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492758,"feature_type":"variation","strand":1,"end":140492760,"alleles":["CCC","CC"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1350830177","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140492762,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492762},{"start":140492766,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140492766,"alleles":["C","G"],"strand":1,"feature_type":"variation","id":"rs918391625","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1045749222","source":"dbSNP","start":140492767,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140492767,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1254556544","clinical_significance":[],"start":140492768,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140492768,"alleles":["C","A","T"],"strand":1,"feature_type":"variation"},{"alleles":["G","A","C"],"end":140492769,"strand":1,"feature_type":"variation","start":140492769,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs905825338","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","A"],"end":140492770,"feature_type":"variation","strand":1,"source":"dbSNP","start":140492770,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1192505423"},{"seq_region_name":"7","id":"rs1795413748","clinical_significance":[],"alleles":["AGGCTGAGGCAGG","AGG"],"end":140492784,"strand":1,"feature_type":"variation","start":140492772,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1369533075","seq_region_name":"7","source":"dbSNP","start":140492774,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140492774,"feature_type":"variation","strand":1},{"id":"rs1795413786","seq_region_name":"7","clinical_significance":[],"start":140492779,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140492779,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140492780,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140492780,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795413799"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1002038816","end":140492784,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140492784,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1563104679","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140492786,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492786,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795413867","alleles":["G","T"],"end":140492790,"feature_type":"variation","strand":1,"source":"dbSNP","start":140492790,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140492793,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140492793,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1038431046"},{"feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140492797,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492797,"clinical_significance":[],"id":"rs933903750","seq_region_name":"7"},{"seq_region_name":"7","id":"rs898555862","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140492800,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492800,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563104685","alleles":["A","G"],"end":140492801,"feature_type":"variation","strand":1,"source":"dbSNP","start":140492801,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["G","A"],"end":140492803,"feature_type":"variation","strand":1,"source":"dbSNP","start":140492803,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1156870713"},{"source":"dbSNP","start":140492806,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140492806,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1363103564"},{"source":"dbSNP","start":140492807,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140492807,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1177133156"},{"seq_region_name":"7","id":"rs1435071005","clinical_significance":[],"start":140492808,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140492808,"alleles":["G","A","C"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140492810,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492810,"source":"dbSNP","seq_region_name":"7","id":"rs771751802","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140492811,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492811,"clinical_significance":[],"id":"rs75345065","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1478449660","feature_type":"variation","strand":1,"end":140492812,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492812},{"seq_region_name":"7","id":"rs1795414117","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140492813,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492813,"source":"dbSNP"},{"alleles":["TT","T"],"end":140492814,"strand":1,"feature_type":"variation","start":140492813,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795414131","clinical_significance":[]},{"alleles":["A","G"],"end":140492817,"feature_type":"variation","strand":1,"source":"dbSNP","start":140492817,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795414159"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492820,"feature_type":"variation","strand":1,"end":140492820,"alleles":["G","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs891420600"},{"seq_region_name":"7","id":"rs1795414201","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","-"],"end":140492823,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492823,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795414217","source":"dbSNP","start":140492828,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140492828,"alleles":["A","G"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492830,"feature_type":"variation","strand":1,"end":140492834,"alleles":["TGCAC","-"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795414235"},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140492831,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492831,"clinical_significance":[],"seq_region_name":"7","id":"rs1795414251"},{"seq_region_name":"7","id":"rs368510346","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492832,"source":"dbSNP","strand":1,"feature_type":"variation","end":140492832,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs529624840","clinical_significance":[],"end":140492837,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140492837,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795414299","alleles":["T","G"],"end":140492838,"feature_type":"variation","strand":1,"source":"dbSNP","start":140492838,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492839,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140492839,"id":"rs1795414325","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","AA"],"end":140492841,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492841,"source":"dbSNP","seq_region_name":"7","id":"rs1795414347","clinical_significance":[]},{"source":"dbSNP","start":140492842,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140492842,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1266040979","seq_region_name":"7"},{"source":"dbSNP","start":140492843,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140492843,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795414382"},{"alleles":["C","G","T"],"end":140492844,"strand":1,"feature_type":"variation","start":140492844,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1438956934","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492847,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140492847,"seq_region_name":"7","id":"rs1795414426","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492850,"source":"dbSNP","strand":1,"feature_type":"variation","end":140492850,"alleles":["T","C"],"seq_region_name":"7","id":"rs1487058454","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492853,"source":"dbSNP","strand":1,"feature_type":"variation","end":140492853,"alleles":["G","A"],"seq_region_name":"7","id":"rs1795414446","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130409543","clinical_significance":[],"strand":1,"feature_type":"variation","end":140492854,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492854,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1017963200","seq_region_name":"7","source":"dbSNP","start":140492856,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140492856,"alleles":["A","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs963720820","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492857,"feature_type":"variation","strand":1,"end":140492857,"alleles":["C","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs979610830","source":"dbSNP","start":140492862,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140492862,"alleles":["C","A","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795414529","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492863,"feature_type":"variation","strand":1,"end":140492863,"alleles":["G","A"]},{"start":140492870,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140492870,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs1210400195","seq_region_name":"7","clinical_significance":[]},{"id":"rs10234306","seq_region_name":"7","clinical_significance":[],"start":140492871,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140492871,"alleles":["G","A","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1054491898","end":140492876,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140492876,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1222620858","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492876,"feature_type":"variation","strand":1,"alleles":["AAAA","-"],"end":140492879},{"start":140492876,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AAAATAAATAAATAAATAAATAAAAATAAATAAA","AAAATAAATAAA"],"end":140492909,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795414705","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["AAATAAATAAATAAATAAATAAA","AAATAAATAAA","AAATAAATAAATAAATAAA","AAATAAATAAATAAATAAATAAATAAA"],"end":140492899,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492877,"clinical_significance":[],"seq_region_name":"7","id":"rs893239484"},{"end":140492879,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140492879,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795414779","clinical_significance":[]},{"id":"rs2130409602","seq_region_name":"7","clinical_significance":[],"start":140492880,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140492880,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492884,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140492884,"seq_region_name":"7","id":"rs956647358","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795414819","seq_region_name":"7","source":"dbSNP","start":140492885,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AAATAAATAAATAAAAATAAATAAA","AAATAAATAAA"],"end":140492909,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs2130409613","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492888,"feature_type":"variation","strand":1,"end":140492888,"alleles":["T","A"]},{"seq_region_name":"7","id":"rs183564214","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140492889,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492889,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492889,"feature_type":"variation","strand":1,"end":140492911,"alleles":["AAATAAATAAAAATAAATAAAAA","AAATAAATAAAAA"],"clinical_significance":[],"seq_region_name":"7","id":"rs1303436095"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795414867","feature_type":"variation","strand":1,"alleles":["T","A","G"],"end":140492892,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492892},{"seq_region_name":"7","id":"rs1393146340","clinical_significance":[],"alleles":["A","G"],"end":140492893,"strand":1,"feature_type":"variation","start":140492893,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1357598398","source":"dbSNP","start":140492895,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140492895,"alleles":["A","G"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140492896,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140492896,"alleles":["T","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130409628"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1466502667","feature_type":"variation","strand":1,"end":140492897,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492897},{"clinical_significance":[],"seq_region_name":"7","id":"rs1175951972","source":"dbSNP","start":140492897,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140492901,"alleles":["AAAAA","AAA","AAAAAA"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["AAATAAATAAA","AAATAAA","AAATAAATAAATAAA"],"end":140492909,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492899,"clinical_significance":[],"seq_region_name":"7","id":"rs1426223434"},{"source":"dbSNP","start":140492900,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140492900,"alleles":["A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1010247135","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1042283600","clinical_significance":[],"start":140492902,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140492902,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs533854020","seq_region_name":"7","feature_type":"variation","strand":1,"end":140492903,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492903},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130409647","alleles":["AAA","AA"],"end":140492905,"feature_type":"variation","strand":1,"source":"dbSNP","start":140492903,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492907,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140492907,"seq_region_name":"7","id":"rs1585517258","clinical_significance":[]},{"seq_region_name":"7","id":"rs1181895162","clinical_significance":[],"start":140492915,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140492915,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140492916,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492916,"source":"dbSNP","seq_region_name":"7","id":"rs987969138","clinical_significance":[]},{"start":140492921,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140492921,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs917747684","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1275402287","alleles":["T","C"],"end":140492922,"feature_type":"variation","strand":1,"source":"dbSNP","start":140492922,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140492930,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["-","G"],"end":140492929,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs199750235"},{"feature_type":"variation","strand":1,"end":140492930,"alleles":["A","AA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492930,"clinical_significance":[],"seq_region_name":"7","id":"rs1795415255"},{"feature_type":"variation","strand":1,"end":140492931,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492931,"clinical_significance":[],"seq_region_name":"7","id":"rs1795415279"},{"end":140492934,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140492934,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs776516701","clinical_significance":[]},{"alleles":["T","A"],"end":140492937,"feature_type":"variation","strand":1,"source":"dbSNP","start":140492937,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1332285792","seq_region_name":"7"},{"seq_region_name":"7","id":"rs2130409675","clinical_significance":[],"start":140492939,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140492939,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1003572892","clinical_significance":[],"alleles":["T","C"],"end":140492953,"strand":1,"feature_type":"variation","start":140492953,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1795415321","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140492954,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492954},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795415342","feature_type":"variation","strand":1,"end":140492956,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492956},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492958,"feature_type":"variation","strand":1,"end":140492958,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1563104719"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795415379","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492959,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140492959},{"alleles":["T","C"],"end":140492961,"feature_type":"variation","strand":1,"source":"dbSNP","start":140492961,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795415396"},{"end":140492962,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140492962,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1034594191","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795415440","clinical_significance":[],"start":140492962,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["GGGG","GGG"],"end":140492965,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1202635831","seq_region_name":"7","alleles":["G","T"],"end":140492964,"feature_type":"variation","strand":1,"source":"dbSNP","start":140492964,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492965,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140492965,"clinical_significance":[],"seq_region_name":"7","id":"rs1795415477"},{"seq_region_name":"7","id":"rs558724099","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492966,"source":"dbSNP","strand":1,"feature_type":"variation","end":140492966,"alleles":["C","T"]},{"source":"dbSNP","start":140492967,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140492967,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1238361274"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795415557","source":"dbSNP","start":140492969,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140492969,"alleles":["T","C"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140492971,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140492971,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs760273392"},{"source":"dbSNP","start":140492974,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140492974,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795415605","seq_region_name":"7"},{"id":"rs1216730334","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140492975,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492975,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1481329027","end":140492980,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140492980,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs372011891","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140492983,"feature_type":"variation","strand":1,"end":140492983,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs949306679","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140492984,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492984,"source":"dbSNP"},{"end":140492988,"alleles":["CTCCC","C"],"strand":1,"feature_type":"variation","start":140492984,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795415716","seq_region_name":"7","clinical_significance":[]},{"id":"rs980627694","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492986,"source":"dbSNP","strand":1,"feature_type":"variation","end":140492986,"alleles":["C","T"]},{"alleles":["C","T"],"end":140492995,"strand":1,"feature_type":"variation","start":140492995,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs35159272","clinical_significance":[]},{"seq_region_name":"7","id":"rs1424297442","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140492997,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140492997,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795415861","source":"dbSNP","start":140492998,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140492998,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140492999,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140492999,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795415879"},{"source":"dbSNP","start":140493000,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140493000,"alleles":["A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs937381695"},{"alleles":["A","G"],"end":140493001,"feature_type":"variation","strand":1,"source":"dbSNP","start":140493001,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1377031257"},{"clinical_significance":[],"id":"rs1795415936","seq_region_name":"7","feature_type":"variation","strand":1,"end":140493003,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493003},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795415951","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493003,"feature_type":"variation","strand":1,"end":140493005,"alleles":["GGG","GG"]},{"id":"rs1016581923","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140493004,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493004,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493009,"source":"dbSNP","strand":1,"feature_type":"variation","end":140493009,"alleles":["G","A"],"seq_region_name":"7","id":"rs1795415999","clinical_significance":[]},{"id":"rs1447773508","seq_region_name":"7","clinical_significance":[],"end":140493013,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140493013,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["A","G"],"end":140493015,"strand":1,"feature_type":"variation","start":140493015,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1415425414","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493018,"source":"dbSNP","strand":1,"feature_type":"variation","end":140493018,"alleles":["G","A"],"seq_region_name":"7","id":"rs2130409789","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493023,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140493023,"id":"rs1402920699","seq_region_name":"7","clinical_significance":[]},{"end":140493026,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140493026,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1038762718","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795416099","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140493033,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493033},{"clinical_significance":[],"seq_region_name":"7","id":"rs1461946968","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493036,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140493036},{"start":140493040,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140493040,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130409805","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1460694034","end":140493043,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140493043,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1369500415","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140493047,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493047,"source":"dbSNP"},{"id":"rs1795416179","seq_region_name":"7","clinical_significance":[],"end":140493048,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140493048,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140493051,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493051,"clinical_significance":[],"seq_region_name":"7","id":"rs1795416204"},{"clinical_significance":[],"seq_region_name":"7","id":"rs188048425","end":140493052,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140493052,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140493058,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140493058,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1167498633","clinical_significance":[]},{"id":"rs11978191","seq_region_name":"7","clinical_significance":[],"start":140493059,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140493059,"alleles":["T","A","C","G"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493061,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140493061,"seq_region_name":"7","id":"rs1795416375","clinical_significance":[]},{"id":"rs535439065","seq_region_name":"7","clinical_significance":[],"end":140493071,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140493071,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493072,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140493072,"seq_region_name":"7","id":"rs1296516054","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1239812393","source":"dbSNP","start":140493073,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140493073,"alleles":["G","A","C"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140493075,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140493075,"alleles":["T","TT"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795416487"},{"end":140493080,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140493080,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795416514","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795416534","alleles":["A","G"],"end":140493081,"feature_type":"variation","strand":1,"source":"dbSNP","start":140493081,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140493083,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493083,"clinical_significance":[],"id":"rs1585517325","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140493088,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493088,"source":"dbSNP","id":"rs1193811986","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130409878","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493101,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140493101},{"clinical_significance":[],"id":"rs1373299587","seq_region_name":"7","source":"dbSNP","start":140493103,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140493103,"alleles":["C","A","G","T"],"feature_type":"variation","strand":1},{"alleles":["C","A","T"],"end":140493104,"strand":1,"feature_type":"variation","start":140493104,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1397096382","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795416654","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493106,"source":"dbSNP","strand":1,"feature_type":"variation","end":140493106,"alleles":["C","G"]},{"end":140493107,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140493107,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795416669"},{"source":"dbSNP","start":140493108,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140493108,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795416687"},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140493109,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493109,"source":"dbSNP","id":"rs1795416706","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493111,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140493111,"clinical_significance":[],"id":"rs1795416722","seq_region_name":"7"},{"id":"rs1795416744","seq_region_name":"7","clinical_significance":[],"start":140493114,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140493114,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140493116,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493116,"clinical_significance":[],"seq_region_name":"7","id":"rs1563104759"},{"clinical_significance":[],"id":"rs1295597070","seq_region_name":"7","end":140493118,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140493118,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140493122,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140493122,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795416820","clinical_significance":[]},{"end":140493126,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140493126,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1353984536"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795416868","alleles":["A","G"],"end":140493127,"feature_type":"variation","strand":1,"source":"dbSNP","start":140493127,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795416892","feature_type":"variation","strand":1,"end":140493144,"alleles":["G","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493144},{"clinical_significance":[],"seq_region_name":"7","id":"rs1232981320","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493148,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140493148},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140493149,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493149,"clinical_significance":[],"seq_region_name":"7","id":"rs180910785"},{"end":140493151,"alleles":["T","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140493151,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795416966"},{"seq_region_name":"7","id":"rs1795416984","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140493155,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493155,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795417010","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493158,"source":"dbSNP","strand":1,"feature_type":"variation","end":140493158,"alleles":["A","G"]},{"clinical_significance":[],"id":"rs1308891844","seq_region_name":"7","source":"dbSNP","start":140493159,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140493159,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs891263043","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493163,"feature_type":"variation","strand":1,"end":140493163,"alleles":["G","A"]},{"end":140493164,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140493164,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795417079"},{"seq_region_name":"7","id":"rs1795417109","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493166,"source":"dbSNP","strand":1,"feature_type":"variation","end":140493166,"alleles":["G","T"]},{"end":140493172,"alleles":["AAAAA","AAAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140493168,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795417132","seq_region_name":"7"},{"source":"dbSNP","start":140493172,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140493172,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1391227844"},{"alleles":["G","T"],"end":140493174,"feature_type":"variation","strand":1,"source":"dbSNP","start":140493174,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1201877556"},{"seq_region_name":"7","id":"rs1585517361","clinical_significance":[],"start":140493178,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140493178,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140493179,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140493179,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795417214"},{"clinical_significance":[],"seq_region_name":"7","id":"rs955227199","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140493182,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493182},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493183,"source":"dbSNP","strand":1,"feature_type":"variation","end":140493183,"alleles":["G","C"],"seq_region_name":"7","id":"rs1008499988","clinical_significance":[]},{"id":"rs1456788133","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140493186,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493186,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1382859332","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493191,"feature_type":"variation","strand":1,"end":140493191,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs185310102","clinical_significance":[],"start":140493192,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","G","T"],"end":140493192,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493193,"source":"dbSNP","strand":1,"feature_type":"variation","end":140493193,"alleles":["T","G"],"seq_region_name":"7","id":"rs1381835596","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs900066817","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140493194,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493194},{"alleles":["G","A"],"end":140493196,"feature_type":"variation","strand":1,"source":"dbSNP","start":140493196,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs553529976"},{"seq_region_name":"7","id":"rs1000567692","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140493200,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493200,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493201,"source":"dbSNP","strand":1,"feature_type":"variation","end":140493201,"alleles":["G","A"],"seq_region_name":"7","id":"rs1795417445","clinical_significance":[]},{"seq_region_name":"7","id":"rs1255233280","clinical_significance":[],"strand":1,"feature_type":"variation","end":140493208,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493208,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1474766498","clinical_significance":[],"start":140493209,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140493209,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140493216,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["ATCTGATCTGA","ATCTGA"],"end":140493226,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1489819559","seq_region_name":"7"},{"alleles":["C","A"],"end":140493218,"feature_type":"variation","strand":1,"source":"dbSNP","start":140493218,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795417513"},{"source":"dbSNP","start":140493219,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140493219,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1194098141","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795417560","clinical_significance":[],"alleles":["G","A"],"end":140493220,"strand":1,"feature_type":"variation","start":140493220,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493228,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140493228,"id":"rs1291169424","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1240901820","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493233,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CCC","CCCC"],"end":140493235},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130410024","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493237,"feature_type":"variation","strand":1,"end":140493237,"alleles":["T","C"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493238,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140493238,"clinical_significance":[],"seq_region_name":"7","id":"rs74323019"},{"seq_region_name":"7","id":"rs191434633","clinical_significance":[],"alleles":["G","A"],"end":140493239,"strand":1,"feature_type":"variation","start":140493239,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493245,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140493245,"seq_region_name":"7","id":"rs1795417773","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795417801","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493246,"feature_type":"variation","strand":1,"end":140493246,"alleles":["T","C"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493247,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140493247,"clinical_significance":[],"seq_region_name":"7","id":"rs1238596638"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795417851","end":140493250,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140493250,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140493255,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140493255,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs564472185"},{"source":"dbSNP","start":140493261,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140493261,"alleles":["T","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs987811480"},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140493263,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493263,"clinical_significance":[],"seq_region_name":"7","id":"rs1795417936"},{"feature_type":"variation","strand":1,"alleles":["G","A","C","T"],"end":140493266,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493266,"clinical_significance":[],"seq_region_name":"7","id":"rs1795417963"},{"seq_region_name":"7","id":"rs1795417995","clinical_significance":[],"start":140493269,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140493269,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140493271,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493271,"clinical_significance":[],"id":"rs1585517398","seq_region_name":"7"},{"start":140493272,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140493272,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs757386931","clinical_significance":[]},{"seq_region_name":"7","id":"rs1385625894","clinical_significance":[],"strand":1,"feature_type":"variation","end":140493273,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493273,"source":"dbSNP"},{"source":"dbSNP","start":140493274,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140493274,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1365454610"},{"id":"rs767734913","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493277,"source":"dbSNP","strand":1,"feature_type":"variation","end":140493277,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795418167","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493278,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140493278},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795418187","feature_type":"variation","strand":1,"end":140493282,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493282},{"end":140493284,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140493284,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1435372279","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140493285,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493285,"source":"dbSNP","id":"rs1361897542","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585517411","clinical_significance":[],"end":140493288,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140493288,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493289,"feature_type":"variation","strand":1,"end":140493289,"alleles":["G","A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs980554246"},{"alleles":["T","-"],"end":140493291,"feature_type":"variation","strand":1,"source":"dbSNP","start":140493291,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795418374"},{"seq_region_name":"7","id":"rs1469254104","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493294,"source":"dbSNP","strand":1,"feature_type":"variation","end":140493294,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130410112","feature_type":"variation","strand":1,"end":140493300,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493300},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493304,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140493304,"seq_region_name":"7","id":"rs1795418443","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795418470","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493312,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140493312},{"start":140493313,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140493313,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130410118","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","AA"],"end":140493318,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493318,"clinical_significance":[],"seq_region_name":"7","id":"rs1377991229"},{"clinical_significance":[],"seq_region_name":"7","id":"rs531837731","feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140493319,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493319},{"clinical_significance":[],"seq_region_name":"7","id":"rs1479427388","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493323,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140493323},{"seq_region_name":"7","id":"rs1795418515","clinical_significance":[],"strand":1,"feature_type":"variation","end":140493326,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493326,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493327,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140493327,"clinical_significance":[],"seq_region_name":"7","id":"rs926588745"},{"start":140493331,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140493331,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795418696","clinical_significance":[]},{"source":"dbSNP","start":140493336,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140493336,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs373446272"},{"seq_region_name":"7","id":"rs1795418743","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140493337,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493337,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493340,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140493340,"clinical_significance":[],"seq_region_name":"7","id":"rs753081829"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1282172202","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493341,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140493341},{"end":140493345,"alleles":["CC","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140493344,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795418819","seq_region_name":"7"},{"alleles":["C","T"],"end":140493345,"feature_type":"variation","strand":1,"source":"dbSNP","start":140493345,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795418845"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493346,"source":"dbSNP","strand":1,"feature_type":"variation","end":140493346,"alleles":["A","G"],"id":"rs2130410163","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1585517445","seq_region_name":"7","source":"dbSNP","start":140493348,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140493348,"alleles":["C","A","T"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493349,"source":"dbSNP","strand":1,"feature_type":"variation","end":140493349,"alleles":["G","A","T"],"seq_region_name":"7","id":"rs575780812","clinical_significance":[]},{"source":"dbSNP","start":140493350,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140493350,"alleles":["C","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs543794877","seq_region_name":"7"},{"alleles":["GGCTCATGC","-"],"end":140493362,"feature_type":"variation","strand":1,"source":"dbSNP","start":140493354,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795418972","seq_region_name":"7"},{"seq_region_name":"7","id":"rs543413323","clinical_significance":[],"start":140493355,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140493355,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1795419015","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493356,"source":"dbSNP","strand":1,"feature_type":"variation","end":140493356,"alleles":["C","A","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493359,"feature_type":"variation","strand":1,"alleles":["A","C","T"],"end":140493359,"clinical_significance":[],"seq_region_name":"7","id":"rs7777753"},{"clinical_significance":[],"id":"rs1222115863","seq_region_name":"7","source":"dbSNP","start":140493360,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140493360,"alleles":["T","C","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795419148","clinical_significance":[],"alleles":["-","T"],"end":140493361,"strand":1,"feature_type":"variation","start":140493362,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795419168","clinical_significance":[],"strand":1,"feature_type":"variation","end":140493362,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493362,"source":"dbSNP"},{"source":"dbSNP","start":140493363,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140493363,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795419188","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1436918085","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493366,"source":"dbSNP","strand":1,"feature_type":"variation","end":140493366,"alleles":["T","C"]},{"end":140493368,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140493368,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795419237","seq_region_name":"7"},{"seq_region_name":"7","id":"rs919879468","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493372,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140493372},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795419295","end":140493374,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140493374,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140493375,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493375,"clinical_significance":[],"seq_region_name":"7","id":"rs930050599"},{"end":140493376,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140493376,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130410224","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493377,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140493377,"id":"rs1271108907","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","C"],"end":140493379,"strand":1,"feature_type":"variation","start":140493379,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1279455867","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1402378283","seq_region_name":"7","alleles":["T","C"],"end":140493380,"feature_type":"variation","strand":1,"source":"dbSNP","start":140493380,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1363702151","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140493381,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493381,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1047152083","alleles":["G","A"],"end":140493382,"feature_type":"variation","strand":1,"source":"dbSNP","start":140493382,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs368263127","clinical_significance":[],"start":140493384,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AGGCCGAAGC","AGGCCGAAGCAGGCCGAAGC"],"end":140493393,"strand":1,"feature_type":"variation"},{"end":140493397,"alleles":["GGCCGAAGCGGGC","GGC"],"strand":1,"feature_type":"variation","start":140493385,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs376554699","clinical_significance":[]},{"seq_region_name":"7","id":"rs181714590","clinical_significance":[],"strand":1,"feature_type":"variation","end":140493388,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493388,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493388,"source":"dbSNP","strand":1,"feature_type":"variation","end":140493398,"alleles":["CGAAGCGGGCG","A"],"seq_region_name":"7","id":"rs386718470","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493389,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140493389,"seq_region_name":"7","id":"rs548140978","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493390,"feature_type":"variation","strand":1,"end":140493391,"alleles":["AA","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585517482"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493391,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140493391,"seq_region_name":"7","id":"rs1235781457","clinical_significance":[]},{"seq_region_name":"7","id":"rs944212781","clinical_significance":[],"start":140493392,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140493392,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140493393,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140493393,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1278177234"},{"strand":1,"feature_type":"variation","end":140493394,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493394,"source":"dbSNP","seq_region_name":"7","id":"rs4726836","clinical_significance":[]},{"source":"dbSNP","start":140493394,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140493398,"alleles":["GGGCG","AGGCA"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs386718471","seq_region_name":"7"},{"source":"dbSNP","start":140493395,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140493395,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1173947337"},{"seq_region_name":"7","id":"rs1217119969","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140493396,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493396,"source":"dbSNP"},{"end":140493397,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140493397,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs2130410289","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140493398,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493398,"clinical_significance":[],"seq_region_name":"7","id":"rs7792629"},{"seq_region_name":"7","id":"rs1585517506","clinical_significance":[],"strand":1,"feature_type":"variation","end":140493399,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493399,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1428333203","clinical_significance":[],"start":140493403,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G","T"],"end":140493403,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1484740887","seq_region_name":"7","feature_type":"variation","strand":1,"end":140493404,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493404},{"strand":1,"feature_type":"variation","alleles":["C","A","G","T"],"end":140493405,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493405,"source":"dbSNP","seq_region_name":"7","id":"rs955407985","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493406,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140493406,"seq_region_name":"7","id":"rs1478723819","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795420274","clinical_significance":[],"start":140493410,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140493410,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563104823","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493412,"feature_type":"variation","strand":1,"end":140493412,"alleles":["C","A","T"]},{"seq_region_name":"7","id":"rs1795420318","clinical_significance":[],"strand":1,"feature_type":"variation","end":140493412,"alleles":["C","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493412,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["A","C","G","T"],"end":140493413,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493413,"source":"dbSNP","seq_region_name":"7","id":"rs4726837","clinical_significance":[]},{"seq_region_name":"7","id":"rs1563104825","clinical_significance":[],"alleles":["A","-"],"end":140493413,"strand":1,"feature_type":"variation","start":140493413,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140493414,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493414,"source":"dbSNP","seq_region_name":"7","id":"rs1454772175","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795420461","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493415,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140493415},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130410352","source":"dbSNP","start":140493416,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140493416,"alleles":["G","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1040265024","clinical_significance":[],"start":140493417,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140493417,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs900117102","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140493420,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493420},{"seq_region_name":"7","id":"rs1393851753","clinical_significance":[],"start":140493423,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140493423,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs570410785","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493425,"source":"dbSNP","strand":1,"feature_type":"variation","end":140493425,"alleles":["C","A"]},{"source":"dbSNP","start":140493426,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140493426,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130410373"},{"seq_region_name":"7","id":"rs1053459319","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140493429,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493429,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140493435,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493435,"clinical_significance":[],"id":"rs1795420594","seq_region_name":"7"},{"start":140493438,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140493438,"alleles":["C","A"],"strand":1,"feature_type":"variation","id":"rs1259037142","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795420643","source":"dbSNP","start":140493439,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140493439,"alleles":["A","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs963936169","clinical_significance":[],"end":140493440,"alleles":["T","C","G"],"strand":1,"feature_type":"variation","start":140493440,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140493441,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140493441,"alleles":["G","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795420697","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1267924640","feature_type":"variation","strand":1,"alleles":["A","T"],"end":140493443,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493443},{"seq_region_name":"7","id":"rs1585517533","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493445,"source":"dbSNP","strand":1,"feature_type":"variation","end":140493445,"alleles":["A","C"]},{"alleles":["C","G","T"],"end":140493449,"feature_type":"variation","strand":1,"source":"dbSNP","start":140493449,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795420739"},{"seq_region_name":"7","id":"rs1434624860","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140493450,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493450,"source":"dbSNP"},{"end":140493451,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140493451,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1319506452","clinical_significance":[]},{"clinical_significance":[],"id":"rs892098209","seq_region_name":"7","end":140493452,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140493452,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["A","AA"],"end":140493458,"feature_type":"variation","strand":1,"source":"dbSNP","start":140493458,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs946055661"},{"alleles":["T","C"],"end":140493460,"strand":1,"feature_type":"variation","start":140493460,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795420870","clinical_significance":[]},{"alleles":["A","G"],"end":140493461,"strand":1,"feature_type":"variation","start":140493461,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs146952387","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493465,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140493465,"clinical_significance":[],"seq_region_name":"7","id":"rs1795420938"},{"seq_region_name":"7","id":"rs1405089235","clinical_significance":[],"alleles":["A","G"],"end":140493467,"strand":1,"feature_type":"variation","start":140493467,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140493468,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140493468,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1563104840","clinical_significance":[]},{"seq_region_name":"7","id":"rs1171074493","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["AAAAAAA","AAAAA","AAAAAA"],"end":140493475,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493469,"source":"dbSNP"},{"end":140493471,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140493471,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1563104850"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1287939373","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140493473,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493473},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140493474,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493474,"clinical_significance":[],"seq_region_name":"7","id":"rs928756779"},{"id":"rs1024702670","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493475,"source":"dbSNP","strand":1,"feature_type":"variation","end":140493475,"alleles":["A","C"]},{"id":"rs1795421099","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140493477,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493477,"source":"dbSNP"},{"clinical_significance":[],"id":"rs970436136","seq_region_name":"7","alleles":["G","A","T"],"end":140493479,"feature_type":"variation","strand":1,"source":"dbSNP","start":140493479,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795421144","end":140493499,"alleles":["CAGGCGTGCTGGCGCAGGC","CAGGC"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140493481,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1300584069","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493482,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140493482},{"start":140493485,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140493485,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1239269206","clinical_significance":[]},{"start":140493486,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140493486,"alleles":["G","A","C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1002077355","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795421247","feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140493487,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493487},{"end":140493489,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140493489,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1240815001"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1239208845","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140493492,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493492},{"id":"rs7806816","seq_region_name":"7","clinical_significance":[],"start":140493493,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140493493,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493494,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140493494,"clinical_significance":[],"seq_region_name":"7","id":"rs1436413231"},{"end":140493495,"alleles":["-","CT"],"strand":1,"feature_type":"variation","start":140493496,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795421498","clinical_significance":[]},{"clinical_significance":[],"id":"rs1272974948","seq_region_name":"7","source":"dbSNP","start":140493496,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140493496,"alleles":["A","G"],"feature_type":"variation","strand":1},{"start":140493497,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140493497,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795421568","clinical_significance":[]},{"id":"rs1585517583","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140493498,"alleles":["G","A","C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493498,"source":"dbSNP"},{"start":140493499,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140493499,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1229390441","clinical_significance":[]},{"seq_region_name":"7","id":"rs963327769","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140493500,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493500,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1314910568","clinical_significance":[],"end":140493501,"alleles":["T","TT"],"strand":1,"feature_type":"variation","start":140493501,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140493511,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140493511,"alleles":["G","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795421695","clinical_significance":[]},{"id":"rs1356508952","seq_region_name":"7","clinical_significance":[],"start":140493514,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140493514,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"alleles":["C","A"],"end":140493517,"strand":1,"feature_type":"variation","start":140493517,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1214735113","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493519,"source":"dbSNP","strand":1,"feature_type":"variation","end":140493519,"alleles":["C","G"],"seq_region_name":"7","id":"rs1795421786","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs776479384","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493520,"feature_type":"variation","strand":1,"end":140493520,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1241800687","end":140493520,"alleles":["G","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140493520,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1316460424","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493520,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GAGCCTGAGG","G"],"end":140493529},{"seq_region_name":"7","id":"rs1195632782","clinical_significance":[],"alleles":["GCCTGAGG","-"],"end":140493529,"strand":1,"feature_type":"variation","start":140493522,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1381522651","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493523,"source":"dbSNP","strand":1,"feature_type":"variation","end":140493523,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1795421973","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140493525,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493525,"source":"dbSNP"},{"seq_region_name":"7","id":"rs938737706","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493526,"source":"dbSNP","strand":1,"feature_type":"variation","end":140493526,"alleles":["G","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs7792789","end":140493529,"alleles":["G","A","C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140493529,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140493531,"alleles":["GCG","ACA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493529,"clinical_significance":[],"seq_region_name":"7","id":"rs386718472"},{"alleles":["C","G","T"],"end":140493530,"strand":1,"feature_type":"variation","start":140493530,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs111274442","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140493531,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140493531,"alleles":["G","A","C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs7792790","seq_region_name":"7"},{"id":"rs942297866","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140493532,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493532,"source":"dbSNP"},{"id":"rs1795422382","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140493533,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493533,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140493535,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493535,"clinical_significance":[],"id":"rs1159658408","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493547,"source":"dbSNP","strand":1,"feature_type":"variation","end":140493547,"alleles":["C","T"],"seq_region_name":"7","id":"rs1795422488","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1410723673","end":140493548,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140493548,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1795422527","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493549,"feature_type":"variation","strand":1,"end":140493549,"alleles":["T","TT"]},{"seq_region_name":"7","id":"rs1399379827","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493550,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140493550},{"end":140493556,"alleles":["AGGC","AGGCAGGC"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140493553,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795422592"},{"clinical_significance":[],"id":"rs1381207948","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493556,"feature_type":"variation","strand":1,"end":140493556,"alleles":["C","A","T"]},{"seq_region_name":"7","id":"rs772782846","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493557,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140493557},{"seq_region_name":"7","id":"rs1585517638","clinical_significance":[],"end":140493559,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140493559,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140493561,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140493561,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795422663","clinical_significance":[]},{"seq_region_name":"7","id":"rs553691808","clinical_significance":[],"strand":1,"feature_type":"variation","end":140493562,"alleles":["T","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493562,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795422706","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140493563,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493563,"source":"dbSNP"},{"end":140493565,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140493565,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs944098359"},{"seq_region_name":"7","id":"rs1442620860","clinical_significance":[],"end":140493566,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140493566,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs112070978","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140493570,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493570,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140493573,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493573,"source":"dbSNP","seq_region_name":"7","id":"rs191890537","clinical_significance":[]},{"seq_region_name":"7","id":"rs1453793001","clinical_significance":[],"start":140493574,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140493574,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1442208096","seq_region_name":"7","alleles":["G","T"],"end":140493576,"feature_type":"variation","strand":1,"source":"dbSNP","start":140493576,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493579,"source":"dbSNP","strand":1,"feature_type":"variation","end":140493579,"alleles":["C","A","T"],"seq_region_name":"7","id":"rs1281223148","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1358064135","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493581,"feature_type":"variation","strand":1,"end":140493581,"alleles":["C","A"]},{"source":"dbSNP","start":140493582,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140493582,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs890892034"},{"start":140493585,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140493585,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795422932","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795422968","seq_region_name":"7","end":140493587,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140493587,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs936947066","clinical_significance":[],"start":140493590,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140493590,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140493592,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493592,"clinical_significance":[],"seq_region_name":"7","id":"rs1054418378"},{"strand":1,"feature_type":"variation","end":140493594,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493594,"source":"dbSNP","seq_region_name":"7","id":"rs1795423059","clinical_significance":[]},{"start":140493600,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140493600,"alleles":["G","C"],"strand":1,"feature_type":"variation","id":"rs1795423081","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","G"],"end":140493604,"feature_type":"variation","strand":1,"source":"dbSNP","start":140493604,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795423098"},{"end":140493607,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140493607,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795423119"},{"start":140493608,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140493608,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795423151","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130410675","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140493611,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493611,"source":"dbSNP"},{"id":"rs1273560386","seq_region_name":"7","clinical_significance":[],"end":140493612,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140493612,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493613,"source":"dbSNP","strand":1,"feature_type":"variation","end":140493613,"alleles":["G","A"],"id":"rs557944312","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs113450539","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140493616,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493616},{"seq_region_name":"7","id":"rs1215827901","clinical_significance":[],"end":140493621,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140493621,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140493628,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493628,"source":"dbSNP","id":"rs186482747","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1011478522","clinical_significance":[],"strand":1,"feature_type":"variation","end":140493629,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493629,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493629,"feature_type":"variation","strand":1,"end":140493629,"alleles":["G","-"],"clinical_significance":[],"seq_region_name":"7","id":"rs1678719227"},{"id":"rs906330221","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140493631,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493631,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493634,"feature_type":"variation","strand":1,"end":140493634,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1021479067"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140493643,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493643,"clinical_significance":[],"seq_region_name":"7","id":"rs967679323"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795423496","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493646,"feature_type":"variation","strand":1,"end":140493646,"alleles":["C","G"]},{"end":140493647,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140493647,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1161631260","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493648,"source":"dbSNP","strand":1,"feature_type":"variation","end":140493648,"alleles":["A","G"],"seq_region_name":"7","id":"rs977464639","clinical_significance":[]},{"seq_region_name":"7","id":"rs561917434","clinical_significance":[],"start":140493649,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140493649,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1795423592","seq_region_name":"7","source":"dbSNP","start":140493656,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140493656,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs960154685","clinical_significance":[],"alleles":["T","C"],"end":140493657,"strand":1,"feature_type":"variation","start":140493657,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140493658,"alleles":["A","C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493658,"clinical_significance":[],"seq_region_name":"7","id":"rs1795423641"},{"seq_region_name":"7","id":"rs1795423662","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493664,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140493664},{"end":140493671,"alleles":["CTCT","CT"],"strand":1,"feature_type":"variation","start":140493668,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1481610364","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140493669,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493669,"clinical_significance":[],"seq_region_name":"7","id":"rs1267427959"},{"strand":1,"feature_type":"variation","alleles":["C","A","G"],"end":140493670,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493670,"source":"dbSNP","seq_region_name":"7","id":"rs1199322679","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1002320419","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493675,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140493675},{"end":140493678,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140493678,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs189683124","clinical_significance":[]},{"source":"dbSNP","start":140493684,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140493684,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1286031291"},{"alleles":["C","A"],"end":140493685,"feature_type":"variation","strand":1,"source":"dbSNP","start":140493685,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1217498059"},{"feature_type":"variation","strand":1,"alleles":["CTTGACTT","CTT"],"end":140493701,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493694,"clinical_significance":[],"seq_region_name":"7","id":"rs1314718231"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493695,"source":"dbSNP","strand":1,"feature_type":"variation","end":140493695,"alleles":["T","C"],"seq_region_name":"7","id":"rs1283327021","clinical_significance":[]},{"seq_region_name":"7","id":"rs1182604517","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493697,"source":"dbSNP","strand":1,"feature_type":"variation","end":140493697,"alleles":["G","T"]},{"id":"rs1219642171","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","-"],"end":140493699,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493699,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1347130905","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140493699,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493699,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795423947","clinical_significance":[],"end":140493700,"alleles":["CT","-"],"strand":1,"feature_type":"variation","start":140493699,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140493700,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140493700,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1281376946","clinical_significance":[]},{"start":140493701,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140493701,"alleles":["T","A"],"strand":1,"feature_type":"variation","id":"rs1795423980","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1404245382","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493707,"source":"dbSNP","strand":1,"feature_type":"variation","end":140493707,"alleles":["T","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563104929","source":"dbSNP","start":140493710,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140493710,"alleles":["T","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1033523475","clinical_significance":[],"end":140493718,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140493718,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1419059051","clinical_significance":[],"strand":1,"feature_type":"variation","end":140493726,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493726,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140493735,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493735,"source":"dbSNP","seq_region_name":"7","id":"rs1795424094","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493736,"feature_type":"variation","strand":1,"end":140493736,"alleles":["G","C"],"clinical_significance":[],"id":"rs1290641412","seq_region_name":"7"},{"source":"dbSNP","start":140493737,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140493737,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1463305722"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130410805","source":"dbSNP","start":140493738,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140493738,"alleles":["C","T"],"feature_type":"variation","strand":1},{"alleles":["C","T"],"end":140493739,"feature_type":"variation","strand":1,"source":"dbSNP","start":140493739,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1344880345"},{"clinical_significance":[],"seq_region_name":"7","id":"rs773944612","source":"dbSNP","start":140493740,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140493740,"alleles":["G","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795424201","clinical_significance":[],"alleles":["GGG","GG"],"end":140493742,"strand":1,"feature_type":"variation","start":140493740,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140493741,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493741,"source":"dbSNP","id":"rs1795424218","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1471198530","source":"dbSNP","start":140493742,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140493742,"alleles":["G","A"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493748,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140493748,"seq_region_name":"7","id":"rs1795424255","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493749,"feature_type":"variation","strand":1,"end":140493749,"alleles":["G","A"],"clinical_significance":[],"id":"rs916113568","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140493754,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493754,"source":"dbSNP","seq_region_name":"7","id":"rs1795424296","clinical_significance":[]},{"seq_region_name":"7","id":"rs1199343123","clinical_significance":[],"end":140493755,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140493755,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795424324","clinical_significance":[],"strand":1,"feature_type":"variation","end":140493756,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493756,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493758,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140493758,"clinical_significance":[],"seq_region_name":"7","id":"rs1393200127"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795424371","source":"dbSNP","start":140493760,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140493760,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1261852519","seq_region_name":"7","alleles":["TA","TATA"],"end":140493762,"feature_type":"variation","strand":1,"source":"dbSNP","start":140493761,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795424412","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493766,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140493766},{"start":140493767,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140493767,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795424438","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140493771,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493771,"source":"dbSNP","seq_region_name":"7","id":"rs1795424453","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140493772,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493772,"clinical_significance":[],"id":"rs942160659","seq_region_name":"7"},{"alleles":["T","C"],"end":140493774,"feature_type":"variation","strand":1,"source":"dbSNP","start":140493774,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130410860"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795424496","end":140493777,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140493777,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs541739743","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493783,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140493783},{"id":"rs372472064","seq_region_name":"7","clinical_significance":[],"alleles":["G","-"],"end":140493784,"strand":1,"feature_type":"variation","start":140493784,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140493784,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140493784,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs560040716","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795424606","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493785,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140493785},{"clinical_significance":[],"seq_region_name":"7","id":"rs151194944","source":"dbSNP","start":140493786,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140493786,"alleles":["G","A","T"],"feature_type":"variation","strand":1},{"start":140493788,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140493788,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585517747","clinical_significance":[]},{"id":"rs1222829934","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140493789,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493789,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795424709","clinical_significance":[],"strand":1,"feature_type":"variation","end":140493790,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493790,"source":"dbSNP"},{"end":140493792,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140493792,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795424721","seq_region_name":"7","clinical_significance":[]},{"id":"rs1795424739","seq_region_name":"7","clinical_significance":[],"start":140493797,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140493797,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140493801,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493801,"source":"dbSNP","seq_region_name":"7","id":"rs1795424754","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140493803,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493803,"source":"dbSNP","seq_region_name":"7","id":"rs2130410902","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1046733843","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493806,"feature_type":"variation","strand":1,"end":140493806,"alleles":["T","G"]},{"seq_region_name":"7","id":"rs1795425001","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493807,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140493807},{"clinical_significance":[],"seq_region_name":"7","id":"rs1297607982","source":"dbSNP","start":140493809,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140493809,"feature_type":"variation","strand":1},{"id":"rs7783010","seq_region_name":"7","clinical_significance":[],"start":140493815,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A","C","G"],"end":140493815,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1795425169","clinical_significance":[],"start":140493816,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140493816,"strand":1,"feature_type":"variation"},{"id":"rs1585517766","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140493819,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493819,"source":"dbSNP"},{"start":140493820,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140493820,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs950602639","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795425231","clinical_significance":[],"start":140493825,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140493825,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs546879482","clinical_significance":[],"start":140493829,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["CC","C"],"end":140493830,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1039416340","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140493832,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493832},{"alleles":["C","G","T"],"end":140493833,"feature_type":"variation","strand":1,"source":"dbSNP","start":140493833,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs770556097"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140493834,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493834,"clinical_significance":[],"id":"rs1795425331","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493843,"feature_type":"variation","strand":1,"end":140493843,"alleles":["C","A"],"clinical_significance":[],"id":"rs1795425356","seq_region_name":"7"},{"seq_region_name":"7","id":"rs776338016","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493844,"source":"dbSNP","strand":1,"feature_type":"variation","end":140493844,"alleles":["C","G"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493845,"feature_type":"variation","strand":1,"end":140493845,"alleles":["C","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs982816907"},{"clinical_significance":[],"id":"rs2130410977","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493852,"feature_type":"variation","strand":1,"end":140493852,"alleles":["A","G"]},{"source":"dbSNP","start":140493855,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140493859,"alleles":["AAAAA","AAAAAA"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795425842","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585517787","feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140493859,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493859},{"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140493860,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493860,"clinical_significance":[],"id":"rs1795425911","seq_region_name":"7"},{"alleles":["A","G"],"end":140493870,"feature_type":"variation","strand":1,"source":"dbSNP","start":140493870,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795425930"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795425950","feature_type":"variation","strand":1,"end":140493872,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493872},{"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140493873,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493873,"clinical_significance":[],"seq_region_name":"7","id":"rs182299925"},{"alleles":["G","A"],"end":140493874,"strand":1,"feature_type":"variation","start":140493874,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1291727789","clinical_significance":[]},{"seq_region_name":"7","id":"rs1355909391","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140493875,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493875,"source":"dbSNP"},{"end":140493876,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140493876,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795426054","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493881,"source":"dbSNP","strand":1,"feature_type":"variation","end":140493881,"alleles":["G","A"],"seq_region_name":"7","id":"rs531286933","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493883,"feature_type":"variation","strand":1,"end":140493883,"alleles":["G","A"],"clinical_significance":[],"id":"rs1795426100","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140493884,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493884,"source":"dbSNP","seq_region_name":"7","id":"rs1795426110","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795426135","seq_region_name":"7","end":140493890,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140493890,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493892,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140493892,"clinical_significance":[],"seq_region_name":"7","id":"rs1795426156"},{"seq_region_name":"7","id":"rs568213801","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493893,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140493893},{"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140493895,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493895,"clinical_significance":[],"seq_region_name":"7","id":"rs1418153332"},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140493901,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493901,"source":"dbSNP","id":"rs1795426230","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585517797","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493904,"source":"dbSNP","strand":1,"feature_type":"variation","end":140493904,"alleles":["A","G"]},{"end":140493905,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140493905,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs374837351"},{"seq_region_name":"7","id":"rs1021850813","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140493906,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493906,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493908,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140493908,"seq_region_name":"7","id":"rs1795426294","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493910,"source":"dbSNP","strand":1,"feature_type":"variation","end":140493910,"alleles":["G","A"],"seq_region_name":"7","id":"rs1462325559","clinical_significance":[]},{"alleles":["G","C"],"end":140493912,"strand":1,"feature_type":"variation","start":140493912,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs187135323","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140493916,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493916,"source":"dbSNP","id":"rs1202850638","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs936858922","clinical_significance":[],"strand":1,"feature_type":"variation","end":140493920,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493920,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1480818924","clinical_significance":[],"strand":1,"feature_type":"variation","end":140493921,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493921,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1795426410","seq_region_name":"7","source":"dbSNP","start":140493936,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140493936,"alleles":["A","G"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140493937,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493937,"clinical_significance":[],"seq_region_name":"7","id":"rs989650854"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795426447","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140493938,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493938},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493945,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140493945,"clinical_significance":[],"id":"rs1795426463","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs759340525","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140493946,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493946},{"clinical_significance":[],"seq_region_name":"7","id":"rs1436103587","source":"dbSNP","start":140493949,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140493949,"feature_type":"variation","strand":1},{"id":"rs1795426522","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140493952,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493952,"source":"dbSNP"},{"end":140493955,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140493955,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1307003956","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","A"],"end":140493962,"feature_type":"variation","strand":1,"source":"dbSNP","start":140493962,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1204477379"},{"alleles":["A","C"],"end":140493964,"feature_type":"variation","strand":1,"source":"dbSNP","start":140493964,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585517817"},{"source":"dbSNP","start":140493965,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140493965,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs535126104","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1258744969","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493966,"source":"dbSNP","strand":1,"feature_type":"variation","end":140493966,"alleles":["T","C"]},{"start":140493973,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140493973,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1248478342","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585517826","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493975,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140493975},{"strand":1,"feature_type":"variation","end":140493977,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493977,"source":"dbSNP","id":"rs2130411108","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs967330104","feature_type":"variation","strand":1,"end":140493978,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493978},{"source":"dbSNP","start":140493979,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140493979,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795426708"},{"alleles":["T","C","G"],"end":140493980,"strand":1,"feature_type":"variation","start":140493980,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs999140743","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140493981,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493981,"source":"dbSNP","seq_region_name":"7","id":"rs1399079054","clinical_significance":[]},{"end":140493985,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140493985,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130411122","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795426787","feature_type":"variation","strand":1,"alleles":["ACAC","AC"],"end":140493990,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493987},{"end":140493988,"alleles":["C","A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140493988,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1393737668"},{"seq_region_name":"7","id":"rs1035732020","clinical_significance":[],"start":140493988,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["CACTCA","CA"],"end":140493993,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140493989,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493989,"source":"dbSNP","seq_region_name":"7","id":"rs764896546","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493990,"source":"dbSNP","strand":1,"feature_type":"variation","end":140493990,"alleles":["C","T"],"seq_region_name":"7","id":"rs1372007622","clinical_significance":[]},{"seq_region_name":"7","id":"rs1313423609","clinical_significance":[],"alleles":["T","A"],"end":140493991,"strand":1,"feature_type":"variation","start":140493991,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140493992,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140493992,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1163625979"},{"source":"dbSNP","start":140493993,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140493993,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1298661657","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140493994,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493994,"clinical_significance":[],"id":"rs1563105013","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493995,"feature_type":"variation","strand":1,"end":140493995,"alleles":["T","G"],"clinical_significance":[],"id":"rs2130411148","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140493997,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140493997,"clinical_significance":[],"seq_region_name":"7","id":"rs1795427019"},{"end":140493998,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140493998,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1383043576","clinical_significance":[]},{"clinical_significance":[],"id":"rs1446105940","seq_region_name":"7","alleles":["C","-"],"end":140493998,"feature_type":"variation","strand":1,"source":"dbSNP","start":140493998,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1563105018","seq_region_name":"7","end":140493998,"alleles":["-","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140493999,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1377182421","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140493999,"source":"dbSNP","strand":1,"feature_type":"variation","end":140493999,"alleles":["A","C","G"]},{"end":140494013,"alleles":["AAAAAAAAAAAAAAA","AAAAAAAAAAAAA","AAAAAAAAAAAAAA","AAAAAAAAAAAAAAAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140493999,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs35901185"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795427192","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494005,"feature_type":"variation","strand":1,"end":140494005,"alleles":["A","C"]},{"seq_region_name":"7","id":"rs1194008106","clinical_significance":[],"start":140494009,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140494009,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs994222420","seq_region_name":"7","source":"dbSNP","start":140494012,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140494012,"alleles":["A","C"],"feature_type":"variation","strand":1},{"id":"rs12536163","seq_region_name":"7","clinical_significance":[],"alleles":["A","C"],"end":140494013,"strand":1,"feature_type":"variation","start":140494013,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140494013,"alleles":["-","AAAAAAAAAAAAAAC","AAC","AC"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494014,"clinical_significance":[],"id":"rs1795427339","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494014,"feature_type":"variation","strand":1,"alleles":["C","CC"],"end":140494014,"clinical_significance":[],"seq_region_name":"7","id":"rs1282565337"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494014,"feature_type":"variation","strand":1,"end":140494014,"alleles":["C","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795427370"},{"strand":1,"feature_type":"variation","end":140494014,"alleles":["C","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494014,"source":"dbSNP","seq_region_name":"7","id":"rs2130411209","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795427411","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["-","T"],"end":140494014,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494015,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1412778869","source":"dbSNP","start":140494015,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140494015,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140494017,"alleles":["G","C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494017,"clinical_significance":[],"seq_region_name":"7","id":"rs1585517884"},{"seq_region_name":"7","id":"rs955254828","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494018,"source":"dbSNP","strand":1,"feature_type":"variation","end":140494018,"alleles":["T","G"]},{"source":"dbSNP","start":140494019,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140494019,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1340146847"},{"seq_region_name":"7","id":"rs1795427523","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494021,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140494021},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494022,"source":"dbSNP","strand":1,"feature_type":"variation","end":140494022,"alleles":["G","A"],"id":"rs1228454877","seq_region_name":"7","clinical_significance":[]},{"start":140494023,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140494023,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585517890","clinical_significance":[]},{"id":"rs1795427581","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140494024,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494024,"source":"dbSNP"},{"id":"rs1795427598","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494025,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140494025},{"end":140494026,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140494026,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1241137178"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494039,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140494039,"clinical_significance":[],"id":"rs1337918104","seq_region_name":"7"},{"id":"rs1795427652","seq_region_name":"7","clinical_significance":[],"end":140494040,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140494040,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140494041,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140494041,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795427672","clinical_significance":[]},{"source":"dbSNP","start":140494044,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140494044,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs757526588","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1391357377","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494052,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140494052},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140494055,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494055,"clinical_significance":[],"seq_region_name":"7","id":"rs1795427743"},{"clinical_significance":[],"id":"rs546994961","seq_region_name":"7","source":"dbSNP","start":140494056,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140494056,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494058,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","G"],"end":140494058,"id":"rs1585517901","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1227681243","source":"dbSNP","start":140494063,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140494063,"alleles":["C","T"],"feature_type":"variation","strand":1},{"id":"rs367907879","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494064,"source":"dbSNP","strand":1,"feature_type":"variation","end":140494064,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795427858","end":140494068,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140494068,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140494069,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140494069,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795427883","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs10952698","source":"dbSNP","start":140494071,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C","T"],"end":140494071,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs374396250","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494074,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140494074},{"seq_region_name":"7","id":"rs767713425","clinical_significance":[],"start":140494076,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140494076,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1795428117","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494078,"source":"dbSNP","strand":1,"feature_type":"variation","end":140494078,"alleles":["G","A"]},{"strand":1,"feature_type":"variation","end":140494081,"alleles":["TTT","TTTT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494079,"source":"dbSNP","id":"rs1255934148","seq_region_name":"7","clinical_significance":[]},{"start":140494083,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140494083,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795428186","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140494084,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494084,"source":"dbSNP","seq_region_name":"7","id":"rs1795428215","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795428243","source":"dbSNP","start":140494089,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140494089,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs963433418","clinical_significance":[],"start":140494091,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140494091,"strand":1,"feature_type":"variation"},{"id":"rs1795428289","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494096,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140494096},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140494099,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494099,"clinical_significance":[],"seq_region_name":"7","id":"rs1418261140"},{"clinical_significance":[],"seq_region_name":"7","id":"rs557641616","source":"dbSNP","start":140494100,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G","T"],"end":140494100,"feature_type":"variation","strand":1},{"end":140494103,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140494103,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1194890712"},{"id":"rs1795428377","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140494105,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494105,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795428396","feature_type":"variation","strand":1,"end":140494107,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494107},{"seq_region_name":"7","id":"rs1795428418","clinical_significance":[],"strand":1,"feature_type":"variation","end":140494112,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494112,"source":"dbSNP"},{"start":140494113,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140494113,"alleles":["A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs973581414","clinical_significance":[]},{"seq_region_name":"7","id":"rs1489897550","clinical_significance":[],"strand":1,"feature_type":"variation","end":140494114,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494114,"source":"dbSNP"},{"clinical_significance":[],"id":"rs919385712","seq_region_name":"7","alleles":["C","G"],"end":140494115,"feature_type":"variation","strand":1,"source":"dbSNP","start":140494115,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494120,"source":"dbSNP","strand":1,"feature_type":"variation","end":140494120,"alleles":["C","T"],"seq_region_name":"7","id":"rs1795428524","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795428542","seq_region_name":"7","alleles":["AAAAA","AAAAAA"],"end":140494126,"feature_type":"variation","strand":1,"source":"dbSNP","start":140494122,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["A","G"],"end":140494123,"feature_type":"variation","strand":1,"source":"dbSNP","start":140494123,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795428567"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494127,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140494127,"seq_region_name":"7","id":"rs1205950112","clinical_significance":[]},{"start":140494129,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140494129,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795428608","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494134,"source":"dbSNP","strand":1,"feature_type":"variation","end":140494134,"alleles":["A","T"],"seq_region_name":"7","id":"rs1353067689","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140494142,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494142,"clinical_significance":[],"seq_region_name":"7","id":"rs1795428641"},{"strand":1,"feature_type":"variation","end":140494147,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494147,"source":"dbSNP","seq_region_name":"7","id":"rs1795428655","clinical_significance":[]},{"id":"rs576219264","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140494148,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494148,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1173711729","seq_region_name":"7","source":"dbSNP","start":140494155,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140494155,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140494158,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140494158,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795428727"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494159,"source":"dbSNP","strand":1,"feature_type":"variation","end":140494159,"alleles":["C","G"],"seq_region_name":"7","id":"rs1396858702","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140494160,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494160,"source":"dbSNP","seq_region_name":"7","id":"rs1285815090","clinical_significance":[]},{"clinical_significance":[],"id":"rs929575413","seq_region_name":"7","alleles":["C","T"],"end":140494166,"feature_type":"variation","strand":1,"source":"dbSNP","start":140494166,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1795428817","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494167,"feature_type":"variation","strand":1,"end":140494167,"alleles":["C","A","T"]},{"start":140494170,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140494170,"strand":1,"feature_type":"variation","id":"rs1795428842","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494174,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140494174,"clinical_significance":[],"seq_region_name":"7","id":"rs1795428864"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1343101394","source":"dbSNP","start":140494176,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140494176,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1052440100","end":140494177,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140494177,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140494180,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494180,"source":"dbSNP","id":"rs1432762791","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1312146115","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494181,"feature_type":"variation","strand":1,"end":140494181,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1795429108","clinical_significance":[],"start":140494182,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140494182,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs750491144","seq_region_name":"7","end":140494185,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140494185,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494187,"feature_type":"variation","strand":1,"end":140494187,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1229058328"},{"alleles":["G","T"],"end":140494188,"strand":1,"feature_type":"variation","start":140494188,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1385440018","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585517942","clinical_significance":[],"strand":1,"feature_type":"variation","end":140494190,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494190,"source":"dbSNP"},{"source":"dbSNP","start":140494199,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140494199,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs750530031"},{"start":140494206,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140494206,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1452879576","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585517949","source":"dbSNP","start":140494208,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140494208,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1429724329","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494209,"feature_type":"variation","strand":1,"end":140494209,"alleles":["A","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585517956","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494215,"feature_type":"variation","strand":1,"end":140494215,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1178519085","clinical_significance":[],"start":140494220,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140494220,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494221,"feature_type":"variation","strand":1,"end":140494221,"alleles":["T","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585517958"},{"end":140494222,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140494222,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795429434","clinical_significance":[]},{"id":"rs537137740","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140494225,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494225,"source":"dbSNP"},{"start":140494227,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140494227,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585517961","clinical_significance":[]},{"id":"rs10952699","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494230,"source":"dbSNP","strand":1,"feature_type":"variation","end":140494230,"alleles":["G","A","C"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494234,"feature_type":"variation","strand":1,"end":140494234,"alleles":["A","C"],"clinical_significance":[],"id":"rs1039321329","seq_region_name":"7"},{"alleles":["GCACGCCACTGCACCCCAGCCTGGGCA","GCACGCCACTGCACCCCAGCCTGGGCACGCCACTGCACCCCAGCCTGGGCA"],"end":140494263,"feature_type":"variation","strand":1,"source":"dbSNP","start":140494237,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1193931228"},{"start":140494238,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140494238,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1434548131","clinical_significance":[]},{"id":"rs1304213665","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494240,"source":"dbSNP","strand":1,"feature_type":"variation","end":140494240,"alleles":["C","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494241,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140494241,"seq_region_name":"7","id":"rs1204757649","clinical_significance":[]},{"id":"rs1350084481","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494248,"source":"dbSNP","strand":1,"feature_type":"variation","end":140494248,"alleles":["C","A","T"]},{"start":140494249,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C","G"],"end":140494249,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs80331552","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1255857188","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494250,"feature_type":"variation","strand":1,"end":140494250,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1351869789","clinical_significance":[],"strand":1,"feature_type":"variation","end":140494251,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494251,"source":"dbSNP"},{"start":140494256,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140494256,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs1207247752","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1011249895","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494258,"feature_type":"variation","strand":1,"end":140494258,"alleles":["T","G"]},{"source":"dbSNP","start":140494259,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140494259,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795429814"},{"alleles":["C","G"],"end":140494262,"strand":1,"feature_type":"variation","start":140494262,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1259312788","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1464138964","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494263,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140494263},{"seq_region_name":"7","id":"rs2130411520","clinical_significance":[],"alleles":["A","AA"],"end":140494266,"strand":1,"feature_type":"variation","start":140494266,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1563105085","seq_region_name":"7","feature_type":"variation","strand":1,"end":140494269,"alleles":["AGAG","AG"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494266},{"alleles":["G","C"],"end":140494267,"strand":1,"feature_type":"variation","start":140494267,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1430873007","seq_region_name":"7","clinical_significance":[]},{"id":"rs1327680058","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140494269,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494269,"source":"dbSNP"},{"alleles":["T","A","G"],"end":140494270,"strand":1,"feature_type":"variation","start":140494270,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1193775157","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140494275,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494275,"clinical_significance":[],"id":"rs1795429952","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs541395955","alleles":["C","A","T"],"end":140494278,"feature_type":"variation","strand":1,"source":"dbSNP","start":140494278,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1451987762","clinical_significance":[],"alleles":["G","A"],"end":140494279,"strand":1,"feature_type":"variation","start":140494279,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs376540581","source":"dbSNP","start":140494284,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140494284,"alleles":["G","A","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1338411256","clinical_significance":[],"start":140494284,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","-"],"end":140494284,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140494285,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G","T"],"end":140494285,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs79209729"},{"clinical_significance":[],"id":"rs34470264","seq_region_name":"7","source":"dbSNP","start":140494285,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140494296,"alleles":["AAAAAAAAAAAA","AAAAAAAAA","AAAAAAAAAA","AAAAAAAAAAA","AAAAAAAAAAAAAA"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494286,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140494286,"seq_region_name":"7","id":"rs1795430176","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795430191","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140494287,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494287,"source":"dbSNP"},{"end":140494292,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140494292,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1563105095","clinical_significance":[]},{"start":140494295,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140494301,"alleles":["AAGATAA","AA"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1371347420","clinical_significance":[]},{"start":140494298,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["ATAAATAAATAAA","ATAAATAAA"],"end":140494310,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795430246","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140494300,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494300,"source":"dbSNP","seq_region_name":"7","id":"rs1795430266","clinical_significance":[]},{"source":"dbSNP","start":140494301,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140494301,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1192752708"},{"source":"dbSNP","start":140494305,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140494305,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795430300","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140494306,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494306,"clinical_significance":[],"seq_region_name":"7","id":"rs1795430315"},{"alleles":["A","G"],"end":140494310,"feature_type":"variation","strand":1,"source":"dbSNP","start":140494310,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795430334"},{"seq_region_name":"7","id":"rs990062334","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140494313,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494313,"source":"dbSNP"},{"seq_region_name":"7","id":"rs10952700","clinical_significance":[],"alleles":["C","A","G","T"],"end":140494314,"strand":1,"feature_type":"variation","start":140494314,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1274401684","end":140494315,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140494315,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140494316,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140494316,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1585518032","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494317,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140494317,"id":"rs1216820002","seq_region_name":"7","clinical_significance":[]},{"end":140494318,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140494318,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1340881687"},{"clinical_significance":[],"seq_region_name":"7","id":"rs903015420","alleles":["T","G"],"end":140494324,"feature_type":"variation","strand":1,"source":"dbSNP","start":140494324,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1227257704","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140494327,"strand":1,"feature_type":"variation","start":140494327,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140494330,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494330,"source":"dbSNP","seq_region_name":"7","id":"rs1795430543","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140494331,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494331,"source":"dbSNP","seq_region_name":"7","id":"rs998815979","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795430593","source":"dbSNP","start":140494338,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140494341,"alleles":["TTTT","TT"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs57639890","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494341,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TGTGTGTGTGTGTG","TGTGTGTGTG","TGTGTGTGTGTG"],"end":140494354},{"clinical_significance":[],"id":"rs147429861","seq_region_name":"7","source":"dbSNP","start":140494342,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140494342,"alleles":["G","A","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563105114","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494344,"feature_type":"variation","strand":1,"end":140494344,"alleles":["G","C","T"]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140494345,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494345,"source":"dbSNP","id":"rs1795430799","seq_region_name":"7","clinical_significance":[]},{"start":140494350,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140494350,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795430817","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494351,"source":"dbSNP","strand":1,"feature_type":"variation","end":140494351,"alleles":["T","C"],"id":"rs1450235079","seq_region_name":"7","clinical_significance":[]},{"id":"rs2130411675","seq_region_name":"7","clinical_significance":[],"start":140494353,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140494353,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130411680","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494354,"feature_type":"variation","strand":1,"end":140494354,"alleles":["G","T"]},{"clinical_significance":[],"id":"rs2130411682","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494355,"feature_type":"variation","strand":1,"end":140494355,"alleles":["A","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795430855","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494362,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140494362},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494364,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140494364,"seq_region_name":"7","id":"rs1795430869","clinical_significance":[]},{"source":"dbSNP","start":140494371,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140494371,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1383122310"},{"seq_region_name":"7","id":"rs1795430905","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494375,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140494375},{"start":140494376,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140494376,"strand":1,"feature_type":"variation","id":"rs1418801495","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1456891720","end":140494377,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140494377,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1326782588","clinical_significance":[],"start":140494380,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140494380,"strand":1,"feature_type":"variation"},{"end":140494381,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140494381,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795430996"},{"end":140494382,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140494382,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585518062","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1159089613","source":"dbSNP","start":140494383,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140494383,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140494384,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494384,"clinical_significance":[],"id":"rs578242595","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1438735568","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494385,"source":"dbSNP","strand":1,"feature_type":"variation","end":140494385,"alleles":["T","C"]},{"end":140494387,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140494387,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795431121","seq_region_name":"7"},{"alleles":["C","T"],"end":140494390,"strand":1,"feature_type":"variation","start":140494390,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795431145","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494392,"feature_type":"variation","strand":1,"end":140494392,"alleles":["C","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1036001976"},{"seq_region_name":"7","id":"rs1336866575","clinical_significance":[],"start":140494393,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140494393,"alleles":["G","A","C"],"strand":1,"feature_type":"variation"},{"alleles":["G","A"],"end":140494397,"strand":1,"feature_type":"variation","start":140494397,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1444474807","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140494401,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494401,"clinical_significance":[],"seq_region_name":"7","id":"rs1233756168"},{"clinical_significance":[],"id":"rs1207256127","seq_region_name":"7","alleles":["C","T"],"end":140494404,"feature_type":"variation","strand":1,"source":"dbSNP","start":140494404,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1795431275","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140494405,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494405,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494409,"source":"dbSNP","strand":1,"feature_type":"variation","end":140494409,"alleles":["C","T"],"seq_region_name":"7","id":"rs1795431290","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795431311","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140494416,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494416},{"clinical_significance":[],"id":"rs1259312071","seq_region_name":"7","feature_type":"variation","strand":1,"end":140494420,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494420},{"seq_region_name":"7","id":"rs1241676209","clinical_significance":[],"start":140494420,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["CA","-"],"end":140494421,"strand":1,"feature_type":"variation"},{"id":"rs1328855351","seq_region_name":"7","clinical_significance":[],"start":140494421,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140494421,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"alleles":["G","GAGTGG"],"end":140494423,"strand":1,"feature_type":"variation","start":140494423,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1213961577","clinical_significance":[]},{"source":"dbSNP","start":140494424,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140494424,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1270303123"},{"feature_type":"variation","strand":1,"end":140494426,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494426,"clinical_significance":[],"id":"rs2130411753","seq_region_name":"7"},{"id":"rs895841435","seq_region_name":"7","clinical_significance":[],"start":140494429,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140494429,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140494430,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494430,"source":"dbSNP","seq_region_name":"7","id":"rs1012938370","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140494431,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494431,"source":"dbSNP","seq_region_name":"7","id":"rs1795431465","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795431488","end":140494432,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140494432,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140494433,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140494433,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795431522"},{"start":140494434,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140494434,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1316800202","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["-","CT"],"end":140494436,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494437,"clinical_significance":[],"seq_region_name":"7","id":"rs2130411774"},{"clinical_significance":[],"seq_region_name":"7","id":"rs11763754","source":"dbSNP","start":140494437,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C","T"],"end":140494437,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs867973016","end":140494440,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140494440,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140494442,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140494442,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs963464184","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130411805","feature_type":"variation","strand":1,"end":140494443,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494443},{"clinical_significance":[],"seq_region_name":"7","id":"rs1279880239","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494445,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140494445},{"feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140494448,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494448,"clinical_significance":[],"seq_region_name":"7","id":"rs1795431707"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494449,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140494449,"id":"rs2130411812","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1444321098","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494450,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140494450},{"start":140494451,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140494451,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs1420770163","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1179453972","clinical_significance":[],"start":140494457,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C","G"],"end":140494457,"strand":1,"feature_type":"variation"},{"end":140494459,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140494459,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1325019555","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795431816","source":"dbSNP","start":140494460,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140494460,"feature_type":"variation","strand":1},{"start":140494464,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140494464,"alleles":["C","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1563105146","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494468,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140494468,"id":"rs1795431846","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494470,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140494470,"seq_region_name":"7","id":"rs868184375","clinical_significance":[]},{"alleles":["G","A","C","T"],"end":140494471,"feature_type":"variation","strand":1,"source":"dbSNP","start":140494471,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1165947565"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1339905712","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494472,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140494472},{"id":"rs1367512378","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494478,"source":"dbSNP","strand":1,"feature_type":"variation","end":140494478,"alleles":["C","A","T"]},{"source":"dbSNP","start":140494481,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140494481,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795431955"},{"feature_type":"variation","strand":1,"end":140494482,"alleles":["A","C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494482,"clinical_significance":[],"id":"rs1396949904","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494490,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140494490,"seq_region_name":"7","id":"rs1795431998","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795432022","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140494494,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494494},{"source":"dbSNP","start":140494496,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140494496,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795432048","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130411859","source":"dbSNP","start":140494498,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140494498,"alleles":["T","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585518134","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494504,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140494504},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494513,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140494513,"clinical_significance":[],"seq_region_name":"7","id":"rs1795432104"},{"clinical_significance":[],"seq_region_name":"7","id":"rs141138891","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494514,"feature_type":"variation","strand":1,"end":140494514,"alleles":["C","T"]},{"alleles":["G","A"],"end":140494515,"feature_type":"variation","strand":1,"source":"dbSNP","start":140494515,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs192987414"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494517,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140494517,"seq_region_name":"7","id":"rs1179272932","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140494518,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494518,"clinical_significance":[],"seq_region_name":"7","id":"rs1795432182"},{"feature_type":"variation","strand":1,"end":140494519,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494519,"clinical_significance":[],"seq_region_name":"7","id":"rs1026522024"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494520,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140494520,"seq_region_name":"7","id":"rs1393671883","clinical_significance":[]},{"id":"rs1795432323","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494524,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140494524},{"clinical_significance":[],"id":"rs1200779661","seq_region_name":"7","source":"dbSNP","start":140494526,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140494526,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1046047048","clinical_significance":[],"end":140494527,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140494527,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1293239379","seq_region_name":"7","clinical_significance":[],"end":140494531,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140494531,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs906173272","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494533,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140494533},{"alleles":["C","G"],"end":140494536,"strand":1,"feature_type":"variation","start":140494536,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1219836168","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795432444","clinical_significance":[],"strand":1,"feature_type":"variation","end":140494541,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494541,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494543,"feature_type":"variation","strand":1,"end":140494543,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795432460"},{"clinical_significance":[],"id":"rs1320690570","seq_region_name":"7","source":"dbSNP","start":140494549,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140494549,"feature_type":"variation","strand":1},{"start":140494550,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140494550,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1234221649","clinical_significance":[]},{"end":140494554,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140494554,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs937786075"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1348266223","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494557,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140494557},{"source":"dbSNP","start":140494559,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140494559,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs950936522"},{"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140494560,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494560,"clinical_significance":[],"seq_region_name":"7","id":"rs1405422344"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1301332222","alleles":["G","T"],"end":140494561,"feature_type":"variation","strand":1,"source":"dbSNP","start":140494561,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs549608369","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140494562,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494562,"source":"dbSNP"},{"start":140494564,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140494564,"strand":1,"feature_type":"variation","id":"rs1436059108","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140494566,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494566,"source":"dbSNP","seq_region_name":"7","id":"rs987764981","clinical_significance":[]},{"seq_region_name":"7","id":"rs1161515600","clinical_significance":[],"start":140494568,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140494568,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140494570,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494570,"clinical_significance":[],"seq_region_name":"7","id":"rs1795432707"},{"seq_region_name":"7","id":"rs1399388541","clinical_significance":[],"end":140494572,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140494572,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1055256998","clinical_significance":[],"start":140494575,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140494575,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1411676062","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494578,"source":"dbSNP","strand":1,"feature_type":"variation","end":140494578,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585518168","alleles":["A","G"],"end":140494580,"feature_type":"variation","strand":1,"source":"dbSNP","start":140494580,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1795432798","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494587,"feature_type":"variation","strand":1,"end":140494587,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs1585518170","clinical_significance":[],"end":140494588,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140494588,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs898897979","clinical_significance":[],"strand":1,"feature_type":"variation","end":140494589,"alleles":["T","A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494589,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795432859","source":"dbSNP","start":140494590,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140494590,"alleles":["G","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795432875","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494597,"source":"dbSNP","strand":1,"feature_type":"variation","end":140494597,"alleles":["G","C"]},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140494602,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494602,"source":"dbSNP","seq_region_name":"7","id":"rs1795432903","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1251358432","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494603,"feature_type":"variation","strand":1,"end":140494603,"alleles":["A","C"]},{"end":140494604,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140494604,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795432956","clinical_significance":[]},{"alleles":["C","T"],"end":140494605,"strand":1,"feature_type":"variation","start":140494605,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1481681441","clinical_significance":[]},{"source":"dbSNP","start":140494609,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140494609,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1270440825","seq_region_name":"7"},{"alleles":["T","C"],"end":140494613,"feature_type":"variation","strand":1,"source":"dbSNP","start":140494613,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1194012159"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494613,"feature_type":"variation","strand":1,"end":140494616,"alleles":["TCCA","TCCATCCA"],"clinical_significance":[],"seq_region_name":"7","id":"rs1481298753"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1250915951","source":"dbSNP","start":140494617,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140494617,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494618,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140494618,"seq_region_name":"7","id":"rs1795433079","clinical_significance":[]},{"start":140494621,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140494621,"alleles":["G","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1475448149","clinical_significance":[]},{"seq_region_name":"7","id":"rs1189798939","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494622,"source":"dbSNP","strand":1,"feature_type":"variation","end":140494622,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1317357866","end":140494623,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140494623,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795433233","clinical_significance":[],"strand":1,"feature_type":"variation","end":140494624,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494624,"source":"dbSNP"},{"source":"dbSNP","start":140494625,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140494625,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs561402409","seq_region_name":"7"},{"end":140494636,"alleles":["AGAGAGAGA","AGAGAGAGAGA"],"strand":1,"feature_type":"variation","start":140494628,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795433265","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494630,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140494630,"clinical_significance":[],"seq_region_name":"7","id":"rs1795433287"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1314920855","source":"dbSNP","start":140494631,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140494631,"alleles":["G","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs2130412019","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494632,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140494632},{"end":140494634,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140494634,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795433326","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494637,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140494637,"id":"rs1420346198","seq_region_name":"7","clinical_significance":[]},{"start":140494640,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140494640,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs528966926","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140494641,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494641,"clinical_significance":[],"seq_region_name":"7","id":"rs1164289018"},{"seq_region_name":"7","id":"rs1373751267","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","G"],"end":140494645,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494645,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1795433409","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494649,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140494649},{"id":"rs1795433451","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140494652,"strand":1,"feature_type":"variation","start":140494652,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1218762539","clinical_significance":[],"strand":1,"feature_type":"variation","end":140494662,"alleles":["AAAAAAAAAA","AAAAAAAAA","AAAAAAAAAAA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494653,"source":"dbSNP"},{"id":"rs1795433495","seq_region_name":"7","clinical_significance":[],"start":140494655,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140494655,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"id":"rs1290916361","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494659,"source":"dbSNP","strand":1,"feature_type":"variation","end":140494659,"alleles":["A","T"]},{"seq_region_name":"7","id":"rs1795433522","clinical_significance":[],"start":140494660,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140494660,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1428824957","clinical_significance":[],"start":140494661,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140494661,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1795433549","clinical_significance":[],"alleles":["A","G"],"end":140494662,"strand":1,"feature_type":"variation","start":140494662,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1388402466","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494663,"source":"dbSNP","strand":1,"feature_type":"variation","end":140494663,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795433585","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494664,"feature_type":"variation","strand":1,"end":140494663,"alleles":["-","AACCATC"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130412071","feature_type":"variation","strand":1,"alleles":["T","A"],"end":140494665,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494665},{"id":"rs1585518201","seq_region_name":"7","clinical_significance":[],"end":140494674,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140494674,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["C","T"],"end":140494677,"strand":1,"feature_type":"variation","start":140494677,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795433620","clinical_significance":[]},{"source":"dbSNP","start":140494678,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140494678,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1337745497"},{"clinical_significance":[],"id":"rs1306732346","seq_region_name":"7","source":"dbSNP","start":140494679,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140494679,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs143951822","alleles":["C","T"],"end":140494682,"feature_type":"variation","strand":1,"source":"dbSNP","start":140494682,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1415854290","feature_type":"variation","strand":1,"end":140494683,"alleles":["G","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494683},{"clinical_significance":[],"seq_region_name":"7","id":"rs1315136890","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494684,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140494684},{"source":"dbSNP","start":140494684,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140494684,"alleles":["C","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795433731"},{"clinical_significance":[],"id":"rs943595107","seq_region_name":"7","source":"dbSNP","start":140494685,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140494685,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1419531575","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494686,"feature_type":"variation","strand":1,"end":140494686,"alleles":["G","A","T"]},{"end":140494689,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140494689,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1227403764","clinical_significance":[]},{"start":140494692,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140494692,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1463240134","clinical_significance":[]},{"source":"dbSNP","start":140494694,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140494694,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1247211838","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494695,"feature_type":"variation","strand":1,"end":140494695,"alleles":["C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585518227"},{"feature_type":"variation","strand":1,"end":140494699,"alleles":["G","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494699,"clinical_significance":[],"id":"rs1204119391","seq_region_name":"7"},{"source":"dbSNP","start":140494704,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140494704,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs995110484","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1462462811","clinical_significance":[],"strand":1,"feature_type":"variation","end":140494705,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494705,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795433915","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494707,"feature_type":"variation","strand":1,"end":140494707,"alleles":["A","T"]},{"seq_region_name":"7","id":"rs1261255411","clinical_significance":[],"start":140494709,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140494709,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795433949","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494714,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140494714},{"id":"rs1295765843","seq_region_name":"7","clinical_significance":[],"end":140494722,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140494722,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140494726,"alleles":["T","A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494726,"clinical_significance":[],"seq_region_name":"7","id":"rs1585518242"},{"id":"rs57565309","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494726,"source":"dbSNP","strand":1,"feature_type":"variation","end":140494727,"alleles":["TT","T"]},{"id":"rs1585518256","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494727,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140494727},{"source":"dbSNP","start":140494728,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140494728,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1308168544"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494729,"source":"dbSNP","strand":1,"feature_type":"variation","end":140494729,"alleles":["G","A"],"id":"rs2130412175","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130412177","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140494732,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494732},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494736,"source":"dbSNP","strand":1,"feature_type":"variation","end":140494736,"alleles":["C","T"],"seq_region_name":"7","id":"rs1224600434","clinical_significance":[]},{"id":"rs1026146179","seq_region_name":"7","clinical_significance":[],"end":140494737,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140494737,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["C","T"],"end":140494738,"strand":1,"feature_type":"variation","start":140494738,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795434158","clinical_significance":[]},{"start":140494740,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140494740,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795434173","clinical_significance":[]},{"seq_region_name":"7","id":"rs149375384","clinical_significance":[],"start":140494741,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140494741,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494743,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140494743,"clinical_significance":[],"seq_region_name":"7","id":"rs1795434219"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1315957923","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140494744,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494744},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140494746,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494746,"source":"dbSNP","seq_region_name":"7","id":"rs1795434236","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795434260","clinical_significance":[],"start":140494748,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140494749,"alleles":["GG","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1212818476","source":"dbSNP","start":140494753,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140494753,"alleles":["T","C"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140494759,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494759,"clinical_significance":[],"seq_region_name":"7","id":"rs1008781269"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494762,"source":"dbSNP","strand":1,"feature_type":"variation","end":140494762,"alleles":["G","C"],"seq_region_name":"7","id":"rs1462882741","clinical_significance":[]},{"clinical_significance":[],"id":"rs1563105217","seq_region_name":"7","source":"dbSNP","start":140494767,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140494767,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795434344","feature_type":"variation","strand":1,"end":140494768,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494768},{"clinical_significance":[],"seq_region_name":"7","id":"rs779897359","source":"dbSNP","start":140494769,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140494769,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494772,"feature_type":"variation","strand":1,"end":140494772,"alleles":["C","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795434374"},{"id":"rs1795434395","seq_region_name":"7","clinical_significance":[],"end":140494773,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140494773,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795434415","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140494775,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494775,"source":"dbSNP"},{"seq_region_name":"7","id":"rs2130412226","clinical_significance":[],"end":140494777,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140494777,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140494780,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140494780,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1354645906","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs539335916","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494782,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140494782},{"feature_type":"variation","strand":1,"end":140494783,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494783,"clinical_significance":[],"id":"rs1795434483","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1171847208","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494785,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140494785},{"clinical_significance":[],"id":"rs1447112782","seq_region_name":"7","feature_type":"variation","strand":1,"end":140494793,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494793},{"alleles":["A","G"],"end":140494797,"feature_type":"variation","strand":1,"source":"dbSNP","start":140494797,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1389215351"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494799,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140494799,"clinical_significance":[],"seq_region_name":"7","id":"rs1795434579"},{"end":140494802,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140494802,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795434608"},{"clinical_significance":[],"id":"rs1183816474","seq_region_name":"7","alleles":["A","T"],"end":140494805,"feature_type":"variation","strand":1,"source":"dbSNP","start":140494805,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140494808,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494808,"source":"dbSNP","seq_region_name":"7","id":"rs965730135","clinical_significance":[]},{"seq_region_name":"7","id":"rs975543433","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494809,"source":"dbSNP","strand":1,"feature_type":"variation","end":140494809,"alleles":["T","C"]},{"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140494815,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494815,"source":"dbSNP","seq_region_name":"7","id":"rs1028854603","clinical_significance":[]},{"clinical_significance":[],"id":"rs1730321752","seq_region_name":"7","source":"dbSNP","start":140494818,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140494818,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140494821,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494821,"clinical_significance":[],"id":"rs1253750108","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs758900166","end":140494824,"alleles":["G","C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140494824,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","A","G"],"end":140494828,"strand":1,"feature_type":"variation","start":140494828,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs4473943","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140494830,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494830,"clinical_significance":[],"seq_region_name":"7","id":"rs989645271"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795434935","source":"dbSNP","start":140494831,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140494831,"alleles":["C","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1203158771","source":"dbSNP","start":140494837,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140494837,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494839,"source":"dbSNP","strand":1,"feature_type":"variation","end":140494839,"alleles":["C","G"],"seq_region_name":"7","id":"rs138457247","clinical_significance":[]},{"alleles":["C","A","T"],"end":140494841,"feature_type":"variation","strand":1,"source":"dbSNP","start":140494841,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs759074344","seq_region_name":"7"},{"source":"dbSNP","start":140494843,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140494843,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795435091"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795435117","end":140494847,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140494847,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140494848,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140494848,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs934469152"},{"feature_type":"variation","strand":1,"end":140494850,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494850,"clinical_significance":[],"seq_region_name":"7","id":"rs1795435170"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1166791521","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140494854,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494854},{"clinical_significance":[],"seq_region_name":"7","id":"rs1381042361","feature_type":"variation","strand":1,"end":140494855,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494855},{"clinical_significance":[],"id":"rs1795435252","seq_region_name":"7","source":"dbSNP","start":140494859,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140494859,"feature_type":"variation","strand":1},{"alleles":["G","A"],"end":140494860,"strand":1,"feature_type":"variation","start":140494860,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795435274","clinical_significance":[]},{"seq_region_name":"7","id":"rs1390142055","clinical_significance":[],"alleles":["C","T"],"end":140494862,"strand":1,"feature_type":"variation","start":140494862,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140494871,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140494871,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs544876734","clinical_significance":[]},{"alleles":["G","A"],"end":140494872,"feature_type":"variation","strand":1,"source":"dbSNP","start":140494872,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1176020220"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795435377","end":140494874,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140494874,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs945637940","feature_type":"variation","strand":1,"end":140494876,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494876},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494878,"source":"dbSNP","strand":1,"feature_type":"variation","end":140494878,"alleles":["A","C"],"seq_region_name":"7","id":"rs1585518316","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494879,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140494879,"seq_region_name":"7","id":"rs1795435452","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795435478","alleles":["C","T"],"end":140494881,"feature_type":"variation","strand":1,"source":"dbSNP","start":140494881,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140494882,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494882,"clinical_significance":[],"seq_region_name":"7","id":"rs1296928968"},{"seq_region_name":"7","id":"rs1376232007","clinical_significance":[],"start":140494882,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","-"],"end":140494882,"strand":1,"feature_type":"variation"},{"alleles":["G","C"],"end":140494883,"strand":1,"feature_type":"variation","start":140494883,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs895749133","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140494885,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494885,"clinical_significance":[],"seq_region_name":"7","id":"rs1795435570"},{"clinical_significance":[],"seq_region_name":"7","id":"rs537199680","alleles":["C","T"],"end":140494887,"feature_type":"variation","strand":1,"source":"dbSNP","start":140494887,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs555610044","clinical_significance":[],"start":140494888,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140494888,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"alleles":["A","G"],"end":140494890,"strand":1,"feature_type":"variation","start":140494890,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1585518337","seq_region_name":"7","clinical_significance":[]},{"end":140494891,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140494891,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs183377361"},{"source":"dbSNP","start":140494892,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140494892,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585518341"},{"start":140494893,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140494893,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585518342","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494896,"source":"dbSNP","strand":1,"feature_type":"variation","end":140494896,"alleles":["T","G"],"seq_region_name":"7","id":"rs1585518347","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494901,"feature_type":"variation","strand":1,"end":140494901,"alleles":["A","G"],"clinical_significance":[],"id":"rs1022973382","seq_region_name":"7"},{"seq_region_name":"7","id":"rs927649346","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140494902,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494902,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1585518355","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140494903,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494903},{"seq_region_name":"7","id":"rs867333415","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494904,"source":"dbSNP","strand":1,"feature_type":"variation","end":140494904,"alleles":["C","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494905,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140494905,"seq_region_name":"7","id":"rs376150775","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494906,"source":"dbSNP","strand":1,"feature_type":"variation","end":140494906,"alleles":["A","G"],"seq_region_name":"7","id":"rs1795435851","clinical_significance":[]},{"clinical_significance":[],"id":"rs937699746","seq_region_name":"7","end":140494908,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140494908,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140494910,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140494910,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1054788491"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494912,"source":"dbSNP","strand":1,"feature_type":"variation","end":140494912,"alleles":["C","T"],"seq_region_name":"7","id":"rs188781978","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494913,"feature_type":"variation","strand":1,"end":140494913,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs930409873"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140494917,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494917,"clinical_significance":[],"seq_region_name":"7","id":"rs1795435957"},{"source":"dbSNP","start":140494919,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140494919,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1047598789"},{"id":"rs886240122","seq_region_name":"7","clinical_significance":[],"end":140494920,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140494920,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494921,"source":"dbSNP","strand":1,"feature_type":"variation","end":140494921,"alleles":["A","C"],"seq_region_name":"7","id":"rs1225042681","clinical_significance":[]},{"source":"dbSNP","start":140494923,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140494923,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130412434"},{"source":"dbSNP","start":140494924,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140494924,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1354453671"},{"seq_region_name":"7","id":"rs1265066364","clinical_significance":[],"end":140494927,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140494927,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs988058281","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494937,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140494937},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795436188","alleles":["AA","-"],"end":140494939,"feature_type":"variation","strand":1,"source":"dbSNP","start":140494938,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1236448292","clinical_significance":[],"end":140494939,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140494939,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1795436249","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494940,"source":"dbSNP","strand":1,"feature_type":"variation","end":140494940,"alleles":["G","A"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494943,"feature_type":"variation","strand":1,"end":140494943,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs577997247"},{"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140494944,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494944,"clinical_significance":[],"seq_region_name":"7","id":"rs964936531"},{"strand":1,"feature_type":"variation","end":140494947,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494947,"source":"dbSNP","id":"rs1795436335","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs974964785","alleles":["T","C"],"end":140494951,"feature_type":"variation","strand":1,"source":"dbSNP","start":140494951,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1216218213","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140494954,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494954},{"end":140494956,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140494956,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1303191518","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494957,"source":"dbSNP","strand":1,"feature_type":"variation","end":140494957,"alleles":["A","C"],"seq_region_name":"7","id":"rs75730896","clinical_significance":[]},{"source":"dbSNP","start":140494957,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AAAAAAAAAAA","AAAAAAAAA","AAAAAAAAAA","AAAAAAAAAAAA"],"end":140494967,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs920965705"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494958,"feature_type":"variation","strand":1,"end":140494958,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795436504"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494963,"feature_type":"variation","strand":1,"end":140494963,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1162278806"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494964,"source":"dbSNP","strand":1,"feature_type":"variation","end":140494964,"alleles":["A","T"],"seq_region_name":"7","id":"rs1795436552","clinical_significance":[]},{"alleles":["AAGAAG","AAG"],"end":140494971,"strand":1,"feature_type":"variation","start":140494966,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795436583","clinical_significance":[]},{"source":"dbSNP","start":140494967,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G","T"],"end":140494967,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs78483591"},{"seq_region_name":"7","id":"rs1795436661","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494967,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AGA","A"],"end":140494969},{"alleles":["G","T"],"end":140494968,"strand":1,"feature_type":"variation","start":140494968,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs978556777","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494969,"source":"dbSNP","strand":1,"feature_type":"variation","end":140494969,"alleles":["A","G"],"seq_region_name":"7","id":"rs1795436729","clinical_significance":[]},{"clinical_significance":[],"id":"rs924371805","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494970,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140494970},{"seq_region_name":"7","id":"rs1795436771","clinical_significance":[],"start":140494980,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140494981,"alleles":["GG","G"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140494981,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494981,"clinical_significance":[],"seq_region_name":"7","id":"rs1795436793"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494984,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140494984,"seq_region_name":"7","id":"rs1472199401","clinical_significance":[]},{"seq_region_name":"7","id":"rs771551889","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494987,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140494987},{"alleles":["G","A"],"end":140494988,"strand":1,"feature_type":"variation","start":140494988,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1057371212","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795436891","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140494990,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140494990,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140494997,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140494997,"clinical_significance":[],"seq_region_name":"7","id":"rs1486951577"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795436936","end":140494998,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140494998,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495000,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140495000,"clinical_significance":[],"seq_region_name":"7","id":"rs1795436962"},{"end":140495002,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140495002,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795436979"},{"start":140495003,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140495003,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1186810694","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs895611976","source":"dbSNP","start":140495004,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140495004,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1795437081","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495011,"feature_type":"variation","strand":1,"end":140495011,"alleles":["C","A"]},{"seq_region_name":"7","id":"rs948655802","clinical_significance":[],"start":140495017,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140495017,"alleles":["A","C","T"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140495022,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495022,"clinical_significance":[],"id":"rs557682869","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs997289600","source":"dbSNP","start":140495024,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140495024,"alleles":["T","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1585518416","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C","T"],"end":140495028,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495028,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1196071820","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495029,"feature_type":"variation","strand":1,"end":140495029,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs1423669758","clinical_significance":[],"start":140495031,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140495031,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1324945928","seq_region_name":"7","feature_type":"variation","strand":1,"end":140495033,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495033},{"id":"rs1795437293","seq_region_name":"7","clinical_significance":[],"start":140495040,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140495040,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1414326933","alleles":["G","A"],"end":140495052,"feature_type":"variation","strand":1,"source":"dbSNP","start":140495052,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1285712939","clinical_significance":[],"start":140495058,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140495058,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140495066,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495066,"clinical_significance":[],"seq_region_name":"7","id":"rs1795437373"},{"end":140495073,"alleles":["TGTGTGTG","TGTGTG"],"strand":1,"feature_type":"variation","start":140495066,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1160249626","clinical_significance":[]},{"id":"rs1795437441","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140495067,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495067,"source":"dbSNP"},{"start":140495073,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140495073,"strand":1,"feature_type":"variation","id":"rs1795437462","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140495075,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140495075,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1028320644","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140495087,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495087,"clinical_significance":[],"seq_region_name":"7","id":"rs1322485406"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495089,"source":"dbSNP","strand":1,"feature_type":"variation","end":140495089,"alleles":["C","G"],"id":"rs1382368781","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585518427","feature_type":"variation","strand":1,"end":140495092,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495092},{"seq_region_name":"7","id":"rs1795437609","clinical_significance":[],"strand":1,"feature_type":"variation","end":140495094,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495094,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1386903482","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495098,"feature_type":"variation","strand":1,"end":140495098,"alleles":["C","G"]},{"source":"dbSNP","start":140495099,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140495099,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1318238246","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1456491247","source":"dbSNP","start":140495104,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140495104,"alleles":["T","C"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140495108,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495108,"clinical_significance":[],"seq_region_name":"7","id":"rs1795437721"},{"seq_region_name":"7","id":"rs1455341205","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140495110,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495110,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1319427067","end":140495114,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140495114,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs117396759","alleles":["G","A","T"],"end":140495115,"feature_type":"variation","strand":1,"source":"dbSNP","start":140495115,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495124,"feature_type":"variation","strand":1,"end":140495124,"alleles":["C","A","G","T"],"clinical_significance":[],"id":"rs1477115036","seq_region_name":"7"},{"id":"rs1795437907","seq_region_name":"7","clinical_significance":[],"end":140495125,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140495125,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs543168893","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495132,"source":"dbSNP","strand":1,"feature_type":"variation","end":140495132,"alleles":["G","A","T"]},{"strand":1,"feature_type":"variation","end":140495141,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495141,"source":"dbSNP","seq_region_name":"7","id":"rs1795437966","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs989488332","alleles":["A","G"],"end":140495144,"feature_type":"variation","strand":1,"source":"dbSNP","start":140495144,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795438018","clinical_significance":[],"start":140495146,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140495146,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140495155,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140495155,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs561164028","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495163,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140495163,"id":"rs1194177913","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585518453","end":140495167,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140495167,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140495176,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495176,"clinical_significance":[],"seq_region_name":"7","id":"rs1795438110"},{"seq_region_name":"7","id":"rs886531624","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495184,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140495184},{"seq_region_name":"7","id":"rs1795438161","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495188,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140495188},{"seq_region_name":"7","id":"rs192951065","clinical_significance":[],"strand":1,"feature_type":"variation","end":140495191,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495191,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795438228","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495193,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140495193},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140495197,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495197,"source":"dbSNP","seq_region_name":"7","id":"rs1208537249","clinical_significance":[]},{"id":"rs545533149","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140495207,"alleles":["TTGATGAACTT","TT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495197,"source":"dbSNP"},{"end":140495199,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140495199,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1462040446"},{"clinical_significance":[],"seq_region_name":"7","id":"rs6959190","end":140495201,"alleles":["T","A","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140495201,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140495202,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140495202,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs966824405"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140495203,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495203,"source":"dbSNP","seq_region_name":"7","id":"rs1795438555","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140495207,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495207,"clinical_significance":[],"seq_region_name":"7","id":"rs1563105270"},{"alleles":["C","G","T"],"end":140495209,"feature_type":"variation","strand":1,"source":"dbSNP","start":140495209,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1019112058"},{"feature_type":"variation","strand":1,"end":140495210,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495210,"clinical_significance":[],"seq_region_name":"7","id":"rs558911816"},{"end":140495212,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140495212,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795438640","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495215,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TT","T"],"end":140495216,"seq_region_name":"7","id":"rs2130412727","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140495219,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495219,"source":"dbSNP","seq_region_name":"7","id":"rs532988441","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795438679","seq_region_name":"7","end":140495223,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140495223,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495224,"source":"dbSNP","strand":1,"feature_type":"variation","end":140495224,"alleles":["G","A"],"id":"rs1795438702","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140495231,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A","C"],"end":140495231,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs996411918","seq_region_name":"7"},{"id":"rs1795438751","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140495237,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495237,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495238,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140495238,"seq_region_name":"7","id":"rs1294909379","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795438797","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495241,"source":"dbSNP","strand":1,"feature_type":"variation","end":140495241,"alleles":["T","C"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495243,"source":"dbSNP","strand":1,"feature_type":"variation","end":140495243,"alleles":["T","C"],"seq_region_name":"7","id":"rs1286061395","clinical_significance":[]},{"source":"dbSNP","start":140495244,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140495244,"alleles":["A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1314859815","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1207093033","source":"dbSNP","start":140495248,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AAA","AA"],"end":140495250,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140495252,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495252,"source":"dbSNP","seq_region_name":"7","id":"rs1336111762","clinical_significance":[]},{"id":"rs764507835","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140495254,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495254,"source":"dbSNP"},{"start":140495257,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140495257,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795438961","clinical_significance":[]},{"seq_region_name":"7","id":"rs1022483996","clinical_significance":[],"alleles":["C","A"],"end":140495260,"strand":1,"feature_type":"variation","start":140495260,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["A","G"],"end":140495262,"feature_type":"variation","strand":1,"source":"dbSNP","start":140495262,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1469011413"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795439043","source":"dbSNP","start":140495263,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140495263,"alleles":["G","A"],"feature_type":"variation","strand":1},{"id":"rs1168521251","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495267,"source":"dbSNP","strand":1,"feature_type":"variation","end":140495267,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs541091480","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495268,"feature_type":"variation","strand":1,"end":140495268,"alleles":["G","A","C"]},{"strand":1,"feature_type":"variation","end":140495270,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495270,"source":"dbSNP","seq_region_name":"7","id":"rs1795439144","clinical_significance":[]},{"source":"dbSNP","start":140495271,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140495271,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1245523895"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495272,"feature_type":"variation","strand":1,"end":140495272,"alleles":["G","A"],"clinical_significance":[],"id":"rs1585518508","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1477975728","seq_region_name":"7","source":"dbSNP","start":140495275,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140495275,"alleles":["C","T"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140495277,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140495277,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1445629221"},{"end":140495278,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140495278,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1178235591","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495279,"feature_type":"variation","strand":1,"end":140495279,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1186086150"},{"seq_region_name":"7","id":"rs990932687","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140495287,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495287,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495288,"source":"dbSNP","strand":1,"feature_type":"variation","end":140495288,"alleles":["C","T"],"seq_region_name":"7","id":"rs1795439376","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs924266710","source":"dbSNP","start":140495291,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","-"],"end":140495291,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495291,"feature_type":"variation","strand":1,"end":140495291,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795439410"},{"source":"dbSNP","start":140495292,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140495292,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795439469"},{"strand":1,"feature_type":"variation","end":140495296,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495296,"source":"dbSNP","id":"rs1274294281","seq_region_name":"7","clinical_significance":[]},{"end":140495298,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140495298,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795439541","seq_region_name":"7","clinical_significance":[]},{"start":140495300,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140495300,"strand":1,"feature_type":"variation","id":"rs1195915735","seq_region_name":"7","clinical_significance":[]},{"end":140495305,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140495305,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs920237185","clinical_significance":[]},{"seq_region_name":"7","id":"rs930389040","clinical_significance":[],"end":140495306,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140495306,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495310,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140495310,"id":"rs551089991","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs377159143","source":"dbSNP","start":140495311,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140495311,"alleles":["G","A","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1394744531","source":"dbSNP","start":140495311,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["GGG","GGGG"],"end":140495313,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140495314,"alleles":["T","A","C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495314,"clinical_significance":[],"seq_region_name":"7","id":"rs12537630"},{"id":"rs1320975199","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495314,"source":"dbSNP","strand":1,"feature_type":"variation","end":140495314,"alleles":["T","-"]},{"seq_region_name":"7","id":"rs1040223632","clinical_significance":[],"alleles":["G","A"],"end":140495315,"strand":1,"feature_type":"variation","start":140495315,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1368719137","end":140495316,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140495316,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563105322","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495317,"feature_type":"variation","strand":1,"alleles":["A","AA"],"end":140495317},{"source":"dbSNP","start":140495317,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140495317,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1585518554","seq_region_name":"7"},{"alleles":["T","G"],"end":140495318,"strand":1,"feature_type":"variation","start":140495318,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1585518557","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs900457963","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495319,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140495319},{"seq_region_name":"7","id":"rs1425493963","clinical_significance":[],"alleles":["C","T"],"end":140495321,"strand":1,"feature_type":"variation","start":140495321,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140495322,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140495322,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs992573973","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130412893","source":"dbSNP","start":140495322,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140495323,"alleles":["CT","-"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140495326,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495326,"source":"dbSNP","seq_region_name":"7","id":"rs1281171538","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1161877274","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495329,"feature_type":"variation","strand":1,"end":140495329,"alleles":["C","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495330,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140495330,"id":"rs530054496","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795440228","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495331,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140495331},{"start":140495335,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140495335,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130412916","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795440247","clinical_significance":[],"end":140495336,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140495336,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495337,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140495337,"seq_region_name":"7","id":"rs917121432","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585518570","feature_type":"variation","strand":1,"end":140495341,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495341},{"source":"dbSNP","start":140495347,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140495347,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs2130412936","seq_region_name":"7"},{"start":140495350,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140495350,"alleles":["A","G"],"strand":1,"feature_type":"variation","id":"rs1227543125","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1288037430","clinical_significance":[],"strand":1,"feature_type":"variation","end":140495351,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495351,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1335687921","clinical_significance":[],"strand":1,"feature_type":"variation","end":140495355,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495355,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1211763129","clinical_significance":[],"start":140495357,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140495357,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1585518581","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140495359,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495359,"source":"dbSNP"},{"end":140495360,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140495360,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1248903996"},{"start":140495364,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140495364,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585518585","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495365,"feature_type":"variation","strand":1,"end":140495365,"alleles":["C","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1204046393"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1291553687","end":140495366,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140495366,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1287846557","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495368,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140495368},{"clinical_significance":[],"seq_region_name":"7","id":"rs1050198367","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495369,"feature_type":"variation","strand":1,"end":140495369,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs948518057","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495373,"source":"dbSNP","strand":1,"feature_type":"variation","end":140495373,"alleles":["C","G"]},{"seq_region_name":"7","id":"rs745459954","clinical_significance":[],"start":140495374,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140495374,"alleles":["T","C","G"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495377,"feature_type":"variation","strand":1,"end":140495377,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs893775662"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585518605","feature_type":"variation","strand":1,"alleles":["T","A"],"end":140495383,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495383},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495391,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140495391,"seq_region_name":"7","id":"rs549170696","clinical_significance":[]},{"source":"dbSNP","start":140495395,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140495395,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1021017636"},{"clinical_significance":[],"seq_region_name":"7","id":"rs966754306","end":140495396,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140495396,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140495400,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495400,"source":"dbSNP","id":"rs1482310966","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs184582132","seq_region_name":"7","feature_type":"variation","strand":1,"end":140495401,"alleles":["G","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495401},{"source":"dbSNP","start":140495402,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","TT"],"end":140495402,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1321826972","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495402,"feature_type":"variation","strand":1,"end":140495402,"alleles":["T","A"],"clinical_significance":[],"id":"rs1795440887","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1035194679","clinical_significance":[],"end":140495404,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140495404,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495405,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140495405,"clinical_significance":[],"seq_region_name":"7","id":"rs1795440967"},{"seq_region_name":"7","id":"rs1475968697","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495406,"source":"dbSNP","strand":1,"feature_type":"variation","end":140495406,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1471876209","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495408,"feature_type":"variation","strand":1,"end":140495408,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1161044745","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495409,"feature_type":"variation","strand":1,"end":140495409,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs959895936","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495410,"source":"dbSNP","strand":1,"feature_type":"variation","end":140495410,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1490362389","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495412,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140495412},{"id":"rs1795441111","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140495414,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495414,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1412483665","clinical_significance":[],"strand":1,"feature_type":"variation","end":140495418,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495418,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495425,"feature_type":"variation","strand":1,"end":140495425,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795441149"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495426,"source":"dbSNP","strand":1,"feature_type":"variation","end":140495426,"alleles":["G","A","C"],"seq_region_name":"7","id":"rs1795441171","clinical_significance":[]},{"seq_region_name":"7","id":"rs1248151935","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140495427,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495427,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140495429,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495429,"source":"dbSNP","seq_region_name":"7","id":"rs1409972786","clinical_significance":[]},{"seq_region_name":"7","id":"rs1450821624","clinical_significance":[],"strand":1,"feature_type":"variation","end":140495435,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495435,"source":"dbSNP"},{"alleles":["A","G"],"end":140495436,"feature_type":"variation","strand":1,"source":"dbSNP","start":140495436,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795441268"},{"strand":1,"feature_type":"variation","end":140495437,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495437,"source":"dbSNP","seq_region_name":"7","id":"rs535107792","clinical_significance":[]},{"seq_region_name":"7","id":"rs920267796","clinical_significance":[],"end":140495438,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140495438,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140495440,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140495440,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1368629873"},{"start":140495443,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140495443,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1409031963","clinical_significance":[]},{"clinical_significance":[],"id":"rs1585518650","seq_region_name":"7","source":"dbSNP","start":140495444,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140495444,"feature_type":"variation","strand":1},{"end":140495450,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140495450,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795441435"},{"source":"dbSNP","start":140495454,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140495454,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1313240685"},{"clinical_significance":[],"id":"rs951670278","seq_region_name":"7","end":140495455,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140495455,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1224279109","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140495457,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495457},{"seq_region_name":"7","id":"rs1369804282","clinical_significance":[],"start":140495458,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140495458,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495459,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140495459,"seq_region_name":"7","id":"rs1795441513","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795441526","alleles":["G","C"],"end":140495467,"feature_type":"variation","strand":1,"source":"dbSNP","start":140495467,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1247304148","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140495468,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495468,"source":"dbSNP"},{"start":140495471,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140495471,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795441563","clinical_significance":[]},{"seq_region_name":"7","id":"rs983098290","clinical_significance":[],"alleles":["G","A"],"end":140495472,"strand":1,"feature_type":"variation","start":140495472,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795441594","clinical_significance":[],"strand":1,"feature_type":"variation","end":140495475,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495475,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795441609","source":"dbSNP","start":140495476,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140495476,"alleles":["G","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1585518669","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495477,"source":"dbSNP","strand":1,"feature_type":"variation","end":140495477,"alleles":["T","G"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495479,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140495479,"seq_region_name":"7","id":"rs1282579670","clinical_significance":[]},{"end":140495480,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140495480,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1292016959"},{"end":140495482,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140495482,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795441676","clinical_significance":[]},{"end":140495484,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140495484,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1435944165"},{"clinical_significance":[],"seq_region_name":"7","id":"rs6464790","end":140495487,"alleles":["C","A","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140495487,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495489,"source":"dbSNP","strand":1,"feature_type":"variation","end":140495489,"alleles":["A","G"],"id":"rs1215229160","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140495490,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495490,"clinical_significance":[],"id":"rs1277474749","seq_region_name":"7"},{"start":140495493,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140495493,"strand":1,"feature_type":"variation","id":"rs775083838","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["TT","T"],"end":140495494,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495493,"clinical_significance":[],"seq_region_name":"7","id":"rs1340615621"},{"end":140495494,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140495494,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1433276232"},{"clinical_significance":[],"id":"rs1204951222","seq_region_name":"7","alleles":["A","C","G"],"end":140495497,"feature_type":"variation","strand":1,"source":"dbSNP","start":140495497,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1426573608","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495498,"feature_type":"variation","strand":1,"end":140495499,"alleles":["CC","C"]},{"clinical_significance":[],"id":"rs1795441915","seq_region_name":"7","source":"dbSNP","start":140495500,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140495500,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140495501,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140495501,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1258678003","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140495503,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495503,"source":"dbSNP","seq_region_name":"7","id":"rs1795441955","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1486835630","feature_type":"variation","strand":1,"alleles":["T","-"],"end":140495507,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495507},{"seq_region_name":"7","id":"rs1585518699","clinical_significance":[],"start":140495510,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140495510,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140495511,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140495511,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795442000"},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140495513,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495513,"clinical_significance":[],"seq_region_name":"7","id":"rs1795442021"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795442043","feature_type":"variation","strand":1,"end":140495515,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495515},{"clinical_significance":[],"id":"rs1795442057","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495517,"feature_type":"variation","strand":1,"end":140495517,"alleles":["A","G"]},{"alleles":["C","T"],"end":140495518,"strand":1,"feature_type":"variation","start":140495518,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1184965436","clinical_significance":[]},{"start":140495519,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140495519,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1242316324","clinical_significance":[]},{"start":140495524,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140495524,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795442113","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795442132","source":"dbSNP","start":140495525,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140495525,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140495527,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495527,"source":"dbSNP","seq_region_name":"7","id":"rs1236473878","clinical_significance":[]},{"id":"rs1795442171","seq_region_name":"7","clinical_significance":[],"alleles":["A","G"],"end":140495530,"strand":1,"feature_type":"variation","start":140495530,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1463372322","feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140495531,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495531},{"seq_region_name":"7","id":"rs1585518713","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495532,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140495532},{"clinical_significance":[],"seq_region_name":"7","id":"rs1475495190","source":"dbSNP","start":140495534,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140495534,"alleles":["C","A"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495536,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140495536,"seq_region_name":"7","id":"rs1795442228","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130413197","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495536,"feature_type":"variation","strand":1,"end":140495539,"alleles":["TCTC","TC"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795442249","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495537,"feature_type":"variation","strand":1,"end":140495537,"alleles":["C","A"]},{"id":"rs1200364393","seq_region_name":"7","clinical_significance":[],"end":140495538,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","start":140495538,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795442300","clinical_significance":[],"start":140495538,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140495538,"alleles":["T","-"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495539,"feature_type":"variation","strand":1,"alleles":["-","AA","AAA","AAAA"],"end":140495538,"clinical_significance":[],"seq_region_name":"7","id":"rs1267493751"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1431573602","alleles":["C","A"],"end":140495539,"feature_type":"variation","strand":1,"source":"dbSNP","start":140495539,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","-"],"end":140495539,"feature_type":"variation","strand":1,"source":"dbSNP","start":140495539,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795442391"},{"seq_region_name":"7","id":"rs1795442423","clinical_significance":[],"end":140495542,"alleles":["AAA","AAAGAAA"],"strand":1,"feature_type":"variation","start":140495540,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795442448","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495540,"feature_type":"variation","strand":1,"alleles":["AAAA","AAAAGAAAA"],"end":140495543},{"seq_region_name":"7","id":"rs763054163","clinical_significance":[],"start":140495540,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AAAAAAAAAAA","AAAAAAAAAA","AAAAAAAAAAAA","AAAAAAAAAAAAA","AAAAAAAAAAAAAA","AAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAA"],"end":140495550,"strand":1,"feature_type":"variation"},{"start":140495543,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140495555,"alleles":["AAAAAAAAGAAAA","AAAA"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795442625","clinical_significance":[]},{"end":140495555,"alleles":["AAAAAAAGAAAA","AAAA"],"strand":1,"feature_type":"variation","start":140495544,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1388301950","seq_region_name":"7","clinical_significance":[]},{"end":140495546,"alleles":["AA","AAGAA"],"strand":1,"feature_type":"variation","start":140495545,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1467988744","clinical_significance":[]},{"start":140495545,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AAAAAAGAAAA","AAAA"],"end":140495555,"strand":1,"feature_type":"variation","id":"rs1795442852","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140495546,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495546,"clinical_significance":[],"seq_region_name":"7","id":"rs1795442885"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795442906","source":"dbSNP","start":140495546,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140495548,"alleles":["AAA","AAAGAAA"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140495546,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140495555,"alleles":["AAAAAGAAAA","AAAA"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1429055059"},{"strand":1,"feature_type":"variation","end":140495546,"alleles":["-","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495547,"source":"dbSNP","seq_region_name":"7","id":"rs1795442962","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795442986","source":"dbSNP","start":140495547,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140495550,"alleles":["AAAA","AAAAAAAAAAAAAGAAAA","AAAAAAAAGAAAA"],"feature_type":"variation","strand":1},{"end":140495569,"alleles":["AAAAGAAAAGAAAAGAAAAGAAA","AAAAGAAAAGAAAAGAAA","AAAAGAAAAGAAAAGAAAAGAAAAGAAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140495547,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1174146303"},{"seq_region_name":"7","id":"rs2130413269","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495548,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AA","AAGAA"],"end":140495549},{"seq_region_name":"7","id":"rs1413376378","clinical_significance":[],"strand":1,"feature_type":"variation","end":140495554,"alleles":["AAAGAAA","AAA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495548,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795443093","clinical_significance":[],"start":140495549,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AA","AAAGAA"],"end":140495550,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495549,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AAGAA","AA"],"end":140495553,"seq_region_name":"7","id":"rs1377056204","clinical_significance":[]},{"seq_region_name":"7","id":"rs1190095027","clinical_significance":[],"strand":1,"feature_type":"variation","end":140495552,"alleles":["AGA","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495550,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140495551,"alleles":["G","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495551,"clinical_significance":[],"seq_region_name":"7","id":"rs7802826"},{"feature_type":"variation","strand":1,"alleles":["G","-"],"end":140495551,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495551,"clinical_significance":[],"seq_region_name":"7","id":"rs200553478"},{"seq_region_name":"7","id":"rs869075157","clinical_significance":[],"start":140495551,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","AAAA"],"end":140495551,"strand":1,"feature_type":"variation"},{"alleles":["AAAA","AAA","AAAAA","AAAAAA","AAAAAAA","AAAAAAAA"],"end":140495555,"strand":1,"feature_type":"variation","start":140495552,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs768084359","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1484168735","feature_type":"variation","strand":1,"end":140495554,"alleles":["AA","AAGAA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495553},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563105391","source":"dbSNP","start":140495553,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140495555,"alleles":["AAA","AAAAGAAA"],"feature_type":"variation","strand":1},{"alleles":["AAAGAAA","AAAGAAAGAAA"],"end":140495559,"feature_type":"variation","strand":1,"source":"dbSNP","start":140495553,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795443464"},{"seq_region_name":"7","id":"rs1308150808","clinical_significance":[],"strand":1,"feature_type":"variation","end":140495555,"alleles":["A","C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495555,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1340088553","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","AAAGA"],"end":140495555,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495555,"source":"dbSNP"},{"seq_region_name":"7","id":"rs2130413316","clinical_significance":[],"alleles":["AGA","A"],"end":140495557,"strand":1,"feature_type":"variation","start":140495555,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140495555,"alleles":["-","AAC","AAT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140495556,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1209561118"},{"source":"dbSNP","start":140495556,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140495556,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs201426210"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795443626","alleles":["G","-"],"end":140495556,"feature_type":"variation","strand":1,"source":"dbSNP","start":140495556,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140495558,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140495558,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795443660"},{"end":140495560,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140495560,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795443667","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1346378763","source":"dbSNP","start":140495561,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140495561,"alleles":["G","A","C"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140495566,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495566,"clinical_significance":[],"seq_region_name":"7","id":"rs1340074453"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1228351744","feature_type":"variation","strand":1,"end":140495570,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495570},{"clinical_significance":[],"seq_region_name":"7","id":"rs1226371668","feature_type":"variation","strand":1,"end":140495571,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495571},{"seq_region_name":"7","id":"rs1281586444","clinical_significance":[],"alleles":["A","T"],"end":140495573,"strand":1,"feature_type":"variation","start":140495573,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795443789","source":"dbSNP","start":140495574,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140495574,"alleles":["A","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585518781","alleles":["T","A","C"],"end":140495575,"feature_type":"variation","strand":1,"source":"dbSNP","start":140495575,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795443837","source":"dbSNP","start":140495578,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140495578,"alleles":["C","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1316104640","source":"dbSNP","start":140495580,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140495580,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795443875","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495581,"feature_type":"variation","strand":1,"alleles":["TT","T"],"end":140495582},{"clinical_significance":[],"seq_region_name":"7","id":"rs907658888","source":"dbSNP","start":140495582,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140495582,"alleles":["T","C","G"],"feature_type":"variation","strand":1},{"alleles":["C","T"],"end":140495583,"feature_type":"variation","strand":1,"source":"dbSNP","start":140495583,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1199078862","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140495584,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495584,"clinical_significance":[],"seq_region_name":"7","id":"rs571548352"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795443950","feature_type":"variation","strand":1,"alleles":["AGGTG","AGGTGAGGTG"],"end":140495589,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495585},{"end":140495588,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140495588,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585518787"},{"id":"rs886441016","seq_region_name":"7","clinical_significance":[],"end":140495589,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140495589,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140495590,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140495590,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795444017","clinical_significance":[]},{"start":140495591,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140495591,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795444047","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495597,"source":"dbSNP","strand":1,"feature_type":"variation","end":140495597,"alleles":["A","G","T"],"seq_region_name":"7","id":"rs944435375","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795444109","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495603,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140495603},{"start":140495604,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140495607,"alleles":["CACA","CA"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795444139","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140495606,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495606,"source":"dbSNP","id":"rs1795444161","seq_region_name":"7","clinical_significance":[]},{"end":140495611,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140495611,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795444177","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795444189","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495611,"feature_type":"variation","strand":1,"alleles":["TTAGG","TTAGGTTAGG"],"end":140495615},{"clinical_significance":[],"seq_region_name":"7","id":"rs538977255","source":"dbSNP","start":140495617,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140495617,"alleles":["G","C"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140495619,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140495619,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795444226"},{"clinical_significance":[],"seq_region_name":"7","id":"rs557089998","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495620,"feature_type":"variation","strand":1,"end":140495620,"alleles":["A","G"]},{"end":140495626,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140495626,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795444255","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1370575780","alleles":["C","T"],"end":140495628,"feature_type":"variation","strand":1,"source":"dbSNP","start":140495628,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1040612744","alleles":["C","T"],"end":140495631,"feature_type":"variation","strand":1,"source":"dbSNP","start":140495631,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1427379162","source":"dbSNP","start":140495632,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140495632,"alleles":["G","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs2130413412","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140495634,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495634,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130413414","feature_type":"variation","strand":1,"end":140495653,"alleles":["ATTCCTTCATTCCTTCATTC","ATTCCTTCATTCCTTCATTCCTTCATTC"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495634},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795444319","feature_type":"variation","strand":1,"end":140495637,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495637},{"seq_region_name":"7","id":"rs1795444338","clinical_significance":[],"strand":1,"feature_type":"variation","end":140495638,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495638,"source":"dbSNP"},{"source":"dbSNP","start":140495639,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140495639,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs189366029"},{"source":"dbSNP","start":140495643,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140495649,"alleles":["TTCCTTC","TTC"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs2130413424","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795444379","clinical_significance":[],"end":140495644,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140495644,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["T","A"],"end":140495648,"feature_type":"variation","strand":1,"source":"dbSNP","start":140495648,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795444396"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495650,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140495650,"clinical_significance":[],"id":"rs1165283190","seq_region_name":"7"},{"end":140495653,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140495653,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795444430"},{"clinical_significance":[],"id":"rs1563105418","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495655,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140495655},{"seq_region_name":"7","id":"rs921752945","clinical_significance":[],"alleles":["C","A","T"],"end":140495659,"strand":1,"feature_type":"variation","start":140495659,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140495660,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140495660,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs931903158","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795444570","feature_type":"variation","strand":1,"end":140495661,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495661},{"end":140495662,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140495662,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795444596","seq_region_name":"7"},{"clinical_significance":[],"id":"rs12534545","seq_region_name":"7","end":140495663,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140495663,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs893035297","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140495664,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495664},{"end":140495665,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140495665,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585518826"},{"seq_region_name":"7","id":"rs1795444820","clinical_significance":[],"strand":1,"feature_type":"variation","end":140495667,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495667,"source":"dbSNP"},{"start":140495670,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140495670,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs554723629","clinical_significance":[]},{"end":140495674,"alleles":["G","A","C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140495674,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs573139668"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1266227815","feature_type":"variation","strand":1,"end":140495675,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495675},{"seq_region_name":"7","id":"rs1464418321","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495681,"source":"dbSNP","strand":1,"feature_type":"variation","end":140495681,"alleles":["T","-"]},{"seq_region_name":"7","id":"rs1795444928","clinical_significance":[],"start":140495682,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140495682,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495686,"feature_type":"variation","strand":1,"end":140495686,"alleles":["C","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1042363660"},{"start":140495687,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140495687,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs902646287","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495688,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140495688,"id":"rs1003546220","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1224762641","clinical_significance":[],"alleles":["A","G"],"end":140495690,"strand":1,"feature_type":"variation","start":140495690,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495691,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140495691,"clinical_significance":[],"seq_region_name":"7","id":"rs1350606534"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795445028","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495697,"feature_type":"variation","strand":1,"end":140495697,"alleles":["A","C"]},{"alleles":["G","A"],"end":140495701,"feature_type":"variation","strand":1,"source":"dbSNP","start":140495701,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs140993256"},{"seq_region_name":"7","id":"rs1795445073","clinical_significance":[],"start":140495702,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140495702,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495704,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140495704,"clinical_significance":[],"seq_region_name":"7","id":"rs959540047"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495705,"source":"dbSNP","strand":1,"feature_type":"variation","end":140495705,"alleles":["T","C"],"seq_region_name":"7","id":"rs1795445103","clinical_significance":[]},{"seq_region_name":"7","id":"rs1407434043","clinical_significance":[],"start":140495708,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140495708,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1369609967","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495709,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140495709},{"seq_region_name":"7","id":"rs968711863","clinical_significance":[],"start":140495712,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140495712,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"end":140495726,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140495726,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1322757203","clinical_significance":[]},{"seq_region_name":"7","id":"rs1012931192","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495728,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140495728},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495728,"feature_type":"variation","strand":1,"end":140495728,"alleles":["A","AA"],"clinical_significance":[],"id":"rs1363120776","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495729,"source":"dbSNP","strand":1,"feature_type":"variation","end":140495729,"alleles":["T","C"],"seq_region_name":"7","id":"rs1795445221","clinical_significance":[]},{"start":140495730,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140495730,"alleles":["G","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1366427661","clinical_significance":[]},{"end":140495746,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140495746,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1027931116","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140495747,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495747,"source":"dbSNP","id":"rs1472847105","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140495749,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140495749,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795445812"},{"end":140495751,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140495751,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs952261404"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495752,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140495752,"id":"rs559349995","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495761,"feature_type":"variation","strand":1,"end":140495761,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1482767298"},{"clinical_significance":[],"seq_region_name":"7","id":"rs370263845","alleles":["GGG","GG"],"end":140495765,"feature_type":"variation","strand":1,"source":"dbSNP","start":140495763,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495765,"feature_type":"variation","strand":1,"end":140495765,"alleles":["G","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795445919"},{"feature_type":"variation","strand":1,"end":140495768,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495768,"clinical_significance":[],"seq_region_name":"7","id":"rs112041748"},{"seq_region_name":"7","id":"rs532892367","clinical_significance":[],"end":140495772,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140495772,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1487713337","clinical_significance":[],"end":140495773,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140495773,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585518882","feature_type":"variation","strand":1,"end":140495774,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495774},{"alleles":["A","G"],"end":140495776,"feature_type":"variation","strand":1,"source":"dbSNP","start":140495776,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1265187910","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1229573751","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495777,"feature_type":"variation","strand":1,"end":140495777,"alleles":["T","C"]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140495780,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495780,"clinical_significance":[],"id":"rs1795446061","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140495782,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495782,"clinical_significance":[],"id":"rs1795446085","seq_region_name":"7"},{"source":"dbSNP","start":140495783,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140495783,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1331904962","seq_region_name":"7"},{"source":"dbSNP","start":140495784,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140495784,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs191102925"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1226115483","source":"dbSNP","start":140495785,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140495785,"alleles":["A","T"],"feature_type":"variation","strand":1},{"end":140495789,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140495789,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585518891","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585518893","clinical_significance":[],"alleles":["G","T"],"end":140495792,"strand":1,"feature_type":"variation","start":140495792,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs975828243","seq_region_name":"7","source":"dbSNP","start":140495793,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140495793,"alleles":["C","T"],"feature_type":"variation","strand":1},{"alleles":["C","T"],"end":140495794,"feature_type":"variation","strand":1,"source":"dbSNP","start":140495794,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs921777409"},{"alleles":["T","C"],"end":140495799,"feature_type":"variation","strand":1,"source":"dbSNP","start":140495799,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795446359"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495803,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140495803,"seq_region_name":"7","id":"rs931855401","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1388107360","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495804,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140495804},{"feature_type":"variation","strand":1,"end":140495805,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495805,"clinical_significance":[],"seq_region_name":"7","id":"rs1795446432"},{"clinical_significance":[],"seq_region_name":"7","id":"rs917021786","source":"dbSNP","start":140495810,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140495810,"alleles":["C","T"],"feature_type":"variation","strand":1},{"start":140495811,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140495811,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs990374803","clinical_significance":[]},{"id":"rs2130413616","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495815,"source":"dbSNP","strand":1,"feature_type":"variation","end":140495815,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585518910","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140495816,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495816},{"source":"dbSNP","start":140495818,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140495818,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs979939956","seq_region_name":"7"},{"start":140495823,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140495823,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1464097819","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495824,"feature_type":"variation","strand":1,"end":140495824,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1156840832"},{"alleles":["T","C"],"end":140495829,"feature_type":"variation","strand":1,"source":"dbSNP","start":140495829,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1472312199"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795446682","source":"dbSNP","start":140495830,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140495830,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795446716","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495833,"source":"dbSNP","strand":1,"feature_type":"variation","end":140495833,"alleles":["G","C"]},{"id":"rs1795446745","seq_region_name":"7","clinical_significance":[],"end":140495837,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140495837,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140495840,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140495840,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795446783","clinical_significance":[]},{"alleles":["C","T"],"end":140495841,"feature_type":"variation","strand":1,"source":"dbSNP","start":140495841,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1213770078"},{"seq_region_name":"7","id":"rs1269421741","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495844,"source":"dbSNP","strand":1,"feature_type":"variation","end":140495844,"alleles":["G","A"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495847,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140495847,"clinical_significance":[],"seq_region_name":"7","id":"rs1795446871"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495857,"source":"dbSNP","strand":1,"feature_type":"variation","end":140495857,"alleles":["G","A"],"seq_region_name":"7","id":"rs1201320717","clinical_significance":[]},{"start":140495858,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140495858,"alleles":["G","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1431609413","clinical_significance":[]},{"source":"dbSNP","start":140495859,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140495859,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795446964","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs914523446","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140495872,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495872},{"source":"dbSNP","start":140495873,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140495873,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795447016","seq_region_name":"7"},{"end":140495875,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140495875,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs2130413688","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs945966237","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140495876,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495876,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495877,"feature_type":"variation","strand":1,"end":140495877,"alleles":["G","A"],"clinical_significance":[],"id":"rs1042375134","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495882,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140495882,"seq_region_name":"7","id":"rs1364191768","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140495887,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495887,"source":"dbSNP","seq_region_name":"7","id":"rs930597622","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795447166","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495891,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140495891},{"end":140495892,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140495892,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795447196"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1266847733","alleles":["T","C"],"end":140495898,"feature_type":"variation","strand":1,"source":"dbSNP","start":140495898,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["A","G"],"end":140495902,"strand":1,"feature_type":"variation","start":140495902,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585518932","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795447268","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140495905,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495905,"source":"dbSNP"},{"end":140495906,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140495906,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130413720","clinical_significance":[]},{"end":140495908,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140495908,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1208590763"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140495911,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495911,"clinical_significance":[],"id":"rs1047634089","seq_region_name":"7"},{"source":"dbSNP","start":140495912,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140495912,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1161666644","seq_region_name":"7"},{"seq_region_name":"7","id":"rs907897509","clinical_significance":[],"start":140495916,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140495916,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140495921,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495921,"clinical_significance":[],"seq_region_name":"7","id":"rs1386708569"},{"strand":1,"feature_type":"variation","end":140495922,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495922,"source":"dbSNP","seq_region_name":"7","id":"rs1329031197","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795447468","clinical_significance":[],"start":140495927,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140495927,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1456839506","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140495934,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495934},{"seq_region_name":"7","id":"rs563159651","clinical_significance":[],"end":140495937,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140495937,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1435616232","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495944,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140495944},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495945,"source":"dbSNP","strand":1,"feature_type":"variation","end":140495945,"alleles":["A","G"],"seq_region_name":"7","id":"rs1795447558","clinical_significance":[]},{"end":140495950,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140495950,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795447583"},{"seq_region_name":"7","id":"rs1367019168","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495956,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140495956},{"seq_region_name":"7","id":"rs1318465847","clinical_significance":[],"end":140495958,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140495958,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["T","C"],"end":140495959,"feature_type":"variation","strand":1,"source":"dbSNP","start":140495959,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1456603263"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795447683","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140495960,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495960},{"id":"rs902627284","seq_region_name":"7","clinical_significance":[],"start":140495965,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AGCAGTAAAGA","A"],"end":140495975,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495967,"feature_type":"variation","strand":1,"end":140495987,"alleles":["CAGTAAAGAACAGTAAAGAAC","CAGTAAAGAAC"],"clinical_significance":[],"seq_region_name":"7","id":"rs71171002"},{"end":140495971,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140495971,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1563105492","clinical_significance":[]},{"clinical_significance":[],"id":"rs1563105498","seq_region_name":"7","end":140495972,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140495972,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495974,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140495974,"clinical_significance":[],"seq_region_name":"7","id":"rs1563105499"},{"clinical_significance":[],"seq_region_name":"7","id":"rs80109830","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495976,"feature_type":"variation","strand":1,"end":140495976,"alleles":["A","G","T"]},{"strand":1,"feature_type":"variation","end":140495979,"alleles":["CAG","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495977,"source":"dbSNP","seq_region_name":"7","id":"rs1392911620","clinical_significance":[]},{"alleles":["A","G"],"end":140495978,"strand":1,"feature_type":"variation","start":140495978,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs74690505","clinical_significance":[]},{"end":140495979,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140495979,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs866398552"},{"seq_region_name":"7","id":"rs1377352931","clinical_significance":[],"strand":1,"feature_type":"variation","end":140495988,"alleles":["GTAAAGAACG","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495979,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795448108","clinical_significance":[],"strand":1,"feature_type":"variation","end":140495986,"alleles":["TAAAGAA","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495980,"source":"dbSNP"},{"alleles":["A","G"],"end":140495981,"strand":1,"feature_type":"variation","start":140495981,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130413808","clinical_significance":[]},{"source":"dbSNP","start":140495981,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140495987,"alleles":["AAAGAAC","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1385624651"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140495983,"source":"dbSNP","strand":1,"feature_type":"variation","end":140495983,"alleles":["A","G"],"seq_region_name":"7","id":"rs1189444488","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130413815","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140495984,"feature_type":"variation","strand":1,"end":140495984,"alleles":["G","T"]},{"end":140495986,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140495986,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs902490236"},{"alleles":["C","T"],"end":140495987,"feature_type":"variation","strand":1,"source":"dbSNP","start":140495987,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs939446680","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1188507242","clinical_significance":[],"alleles":["G","A"],"end":140495988,"strand":1,"feature_type":"variation","start":140495988,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1585518985","clinical_significance":[],"start":140495997,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["ACAGAAGCTGGCTACA","ACA"],"end":140496012,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1056529529","source":"dbSNP","start":140496003,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140496003,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs895203446","clinical_significance":[],"end":140496010,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140496010,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795448321","feature_type":"variation","strand":1,"end":140496011,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496011},{"seq_region_name":"7","id":"rs1043875550","clinical_significance":[],"end":140496014,"alleles":["AAA","AAAA"],"strand":1,"feature_type":"variation","start":140496012,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1012446089","source":"dbSNP","start":140496013,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140496013,"alleles":["A","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs530810570","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140496014,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496014,"source":"dbSNP"},{"start":140496017,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140496017,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795448462","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496024,"feature_type":"variation","strand":1,"end":140496024,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585519001"},{"clinical_significance":[],"id":"rs1292160604","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496030,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140496030},{"clinical_significance":[],"seq_region_name":"7","id":"rs904018068","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140496033,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496033},{"clinical_significance":[],"id":"rs1028234307","seq_region_name":"7","end":140496034,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140496034,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140496036,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496036,"source":"dbSNP","seq_region_name":"7","id":"rs1279174489","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795448628","clinical_significance":[],"start":140496042,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140496042,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1795448651","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140496043,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496043,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["-","TTTTT"],"end":140496044,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496045,"clinical_significance":[],"seq_region_name":"7","id":"rs1795448685"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585519009","source":"dbSNP","start":140496045,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140496045,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs144601373","source":"dbSNP","start":140496046,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TTTTCTTTT","TTTTCTTTTCTTTT"],"end":140496054,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496051,"feature_type":"variation","strand":1,"alleles":["TTTTGTTTT","TTTT"],"end":140496059,"clinical_significance":[],"id":"rs1795448804","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs71173203","feature_type":"variation","strand":1,"alleles":["-","C"],"end":140496054,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496055},{"source":"dbSNP","start":140496055,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C","T"],"end":140496055,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs10247166"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496059,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140496059,"seq_region_name":"7","id":"rs1795448923","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140496060,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496060,"clinical_significance":[],"seq_region_name":"7","id":"rs116040904"},{"start":140496060,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["CTTTTTTTTG","-"],"end":140496069,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795448998","clinical_significance":[]},{"start":140496061,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140496061,"alleles":["T","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585519025","clinical_significance":[]},{"start":140496061,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140496068,"alleles":["TTTTTTTT","TTTT","TTTTTTT","TTTTTTTTT"],"strand":1,"feature_type":"variation","id":"rs1429741480","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795449094","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140496064,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496064,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1000219011","clinical_significance":[],"strand":1,"feature_type":"variation","end":140496081,"alleles":["TTTTTGTTTTTGTTTTTG","TTTTTGTTTTTGTTTTTGTTTTTG"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496064,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs114278782","alleles":["T","C"],"end":140496065,"feature_type":"variation","strand":1,"source":"dbSNP","start":140496065,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496069,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140496069,"seq_region_name":"7","id":"rs1440084007","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795449222","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496069,"feature_type":"variation","strand":1,"end":140496069,"alleles":["G","-"]},{"end":140496070,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140496070,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795449254","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795449278","feature_type":"variation","strand":1,"end":140496074,"alleles":["TTTTT","TTTT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496070},{"source":"dbSNP","start":140496075,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C","T"],"end":140496075,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585519041"},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140496081,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496081,"clinical_significance":[],"seq_region_name":"7","id":"rs2130413928"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585519044","end":140496084,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140496084,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140496085,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496085,"source":"dbSNP","id":"rs1169476305","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140496086,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496086,"source":"dbSNP","seq_region_name":"7","id":"rs1585519049","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795449496","clinical_significance":[],"start":140496089,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140496089,"strand":1,"feature_type":"variation"},{"start":140496090,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140496090,"alleles":["A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1431805611","clinical_significance":[]},{"source":"dbSNP","start":140496091,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140496091,"alleles":["T","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1388521853"},{"seq_region_name":"7","id":"rs1168392895","clinical_significance":[],"start":140496092,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140496092,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs549331894","clinical_significance":[],"start":140496093,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140496093,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"start":140496094,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G","T"],"end":140496094,"strand":1,"feature_type":"variation","id":"rs1795449630","seq_region_name":"7","clinical_significance":[]},{"start":140496097,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140496097,"alleles":["G","T"],"strand":1,"feature_type":"variation","id":"rs1209167856","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1185973256","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496099,"feature_type":"variation","strand":1,"end":140496099,"alleles":["T","C"]},{"alleles":["AA","A"],"end":140496102,"strand":1,"feature_type":"variation","start":140496101,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795449725","clinical_significance":[]},{"source":"dbSNP","start":140496102,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140496101,"alleles":["-","T","TT"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795449749"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496102,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140496102,"seq_region_name":"7","id":"rs1483860687","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1213844018","feature_type":"variation","strand":1,"alleles":["TTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTT","TTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT"],"end":140496124,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496103},{"seq_region_name":"7","id":"rs2130413991","clinical_significance":[],"start":140496104,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140496103,"alleles":["-","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795449987","source":"dbSNP","start":140496113,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140496112,"alleles":["-","C"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496114,"feature_type":"variation","strand":1,"end":140496113,"alleles":["-","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795450012"},{"source":"dbSNP","start":140496118,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140496118,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795450039"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795450061","source":"dbSNP","start":140496124,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TG","-"],"end":140496125,"feature_type":"variation","strand":1},{"alleles":["-","TTA"],"end":140496124,"feature_type":"variation","strand":1,"source":"dbSNP","start":140496125,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795450088"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1242440307","alleles":["G","-"],"end":140496125,"feature_type":"variation","strand":1,"source":"dbSNP","start":140496125,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140496125,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496125,"clinical_significance":[],"id":"rs1251080300","seq_region_name":"7"},{"end":140496126,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140496126,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1483946652","seq_region_name":"7","clinical_significance":[]},{"end":140496127,"alleles":["G","C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140496127,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs112372511"},{"source":"dbSNP","start":140496129,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140496129,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795450213"},{"alleles":["G","A"],"end":140496130,"feature_type":"variation","strand":1,"source":"dbSNP","start":140496130,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1410082282"},{"id":"rs1585519072","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140496132,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496132,"source":"dbSNP"},{"start":140496133,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140496133,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1472400603","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795450319","clinical_significance":[],"start":140496134,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140496134,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795450338","source":"dbSNP","start":140496135,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140496135,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1369016473","feature_type":"variation","strand":1,"alleles":["CTCACTC","CTC"],"end":140496141,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496135},{"source":"dbSNP","start":140496136,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140496136,"alleles":["T","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1328416044"},{"start":140496138,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140496138,"alleles":["A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585519080","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496139,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CTCT","CT"],"end":140496142,"seq_region_name":"7","id":"rs1406331208","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496142,"source":"dbSNP","strand":1,"feature_type":"variation","end":140496142,"alleles":["T","-"],"seq_region_name":"7","id":"rs1795450442","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496143,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140496143,"clinical_significance":[],"seq_region_name":"7","id":"rs1585519083"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1416323010","feature_type":"variation","strand":1,"end":140496144,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496144},{"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140496146,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496146,"clinical_significance":[],"seq_region_name":"7","id":"rs1795450515"},{"seq_region_name":"7","id":"rs1795450537","clinical_significance":[],"end":140496149,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140496149,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1585519089","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496150,"source":"dbSNP","strand":1,"feature_type":"variation","end":140496150,"alleles":["A","C"]},{"seq_region_name":"7","id":"rs1795450583","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496151,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140496151},{"end":140496152,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140496152,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1162011279"},{"clinical_significance":[],"id":"rs1795450634","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140496156,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496156},{"id":"rs1585519093","seq_region_name":"7","clinical_significance":[],"start":140496157,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140496157,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496158,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140496158,"id":"rs1795450684","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496159,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140496159,"clinical_significance":[],"seq_region_name":"7","id":"rs1472728779"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1413317733","feature_type":"variation","strand":1,"end":140496162,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496162},{"seq_region_name":"7","id":"rs1165702226","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496163,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140496163},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140496165,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496165,"clinical_significance":[],"seq_region_name":"7","id":"rs1473285598"},{"end":140496166,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140496166,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1249241920"},{"feature_type":"variation","strand":1,"end":140496167,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496167,"clinical_significance":[],"seq_region_name":"7","id":"rs1370276520"},{"seq_region_name":"7","id":"rs1291712883","clinical_significance":[],"alleles":["G","A"],"end":140496168,"strand":1,"feature_type":"variation","start":140496168,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1585519110","clinical_significance":[],"alleles":["A","C"],"end":140496171,"strand":1,"feature_type":"variation","start":140496171,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140496173,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496173,"clinical_significance":[],"seq_region_name":"7","id":"rs1795450905"},{"seq_region_name":"7","id":"rs1456409789","clinical_significance":[],"start":140496176,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140496176,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140496177,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496177,"source":"dbSNP","seq_region_name":"7","id":"rs567459522","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795450986","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496183,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140496183},{"seq_region_name":"7","id":"rs1585519116","clinical_significance":[],"alleles":["A","C"],"end":140496187,"strand":1,"feature_type":"variation","start":140496187,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["C","A"],"end":140496189,"feature_type":"variation","strand":1,"source":"dbSNP","start":140496189,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1397833224","seq_region_name":"7"},{"seq_region_name":"7","id":"rs2130414094","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140496190,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496190,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1306531643","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496192,"feature_type":"variation","strand":1,"end":140496192,"alleles":["C","A","T"]},{"strand":1,"feature_type":"variation","end":140496193,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496193,"source":"dbSNP","id":"rs1350198723","seq_region_name":"7","clinical_significance":[]},{"start":140496194,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140496194,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1415048078","clinical_significance":[]},{"seq_region_name":"7","id":"rs1348648170","clinical_significance":[],"start":140496197,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140496197,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1314345342","seq_region_name":"7","alleles":["C","A","T"],"end":140496198,"feature_type":"variation","strand":1,"source":"dbSNP","start":140496198,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1319416922","clinical_significance":[],"start":140496199,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140496199,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140496200,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496200,"clinical_significance":[],"id":"rs1795451268","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1243415243","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496201,"feature_type":"variation","strand":1,"end":140496201,"alleles":["A","G"]},{"feature_type":"variation","strand":1,"end":140496205,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496205,"clinical_significance":[],"seq_region_name":"7","id":"rs1795451323"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795451346","end":140496207,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140496207,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1344184125","seq_region_name":"7","clinical_significance":[],"start":140496209,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140496209,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1202880983","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140496210,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496210},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140496212,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496212,"source":"dbSNP","seq_region_name":"7","id":"rs896707385","clinical_significance":[]},{"id":"rs1250843381","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496214,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140496214},{"seq_region_name":"7","id":"rs1485837991","clinical_significance":[],"start":140496215,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140496215,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs11980241","clinical_significance":[],"end":140496219,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","start":140496219,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140496220,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496220,"source":"dbSNP","seq_region_name":"7","id":"rs2130414152","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1422209458","source":"dbSNP","start":140496221,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140496221,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795451673","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","-"],"end":140496224,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496224,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795451691","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140496226,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496226,"source":"dbSNP"},{"id":"rs1008291333","seq_region_name":"7","clinical_significance":[],"start":140496230,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","G"],"end":140496230,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140496231,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140496231,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1164138167"},{"seq_region_name":"7","id":"rs1391382040","clinical_significance":[],"alleles":["A","G","T"],"end":140496232,"strand":1,"feature_type":"variation","start":140496232,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496233,"feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140496233,"clinical_significance":[],"id":"rs1432190884","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1167213652","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496234,"feature_type":"variation","strand":1,"end":140496234,"alleles":["G","A"]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140496235,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496235,"clinical_significance":[],"id":"rs1196558543","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1467855695","clinical_significance":[],"end":140496238,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140496238,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1795451896","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140496241,"strand":1,"feature_type":"variation","start":140496241,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795451925","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496243,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140496243},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496244,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140496244,"id":"rs1449132634","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["CTACAGGCGCCCGCCACCAAGCCCGGCTA","CTA"],"end":140496272,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496244,"clinical_significance":[],"id":"rs1370338017","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496245,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140496245,"id":"rs1304285690","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1376512788","source":"dbSNP","start":140496247,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140496247,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1283589906","clinical_significance":[],"start":140496248,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140496248,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585519160","feature_type":"variation","strand":1,"end":140496249,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496249},{"seq_region_name":"7","id":"rs1219863441","clinical_significance":[],"end":140496251,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140496251,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795452160","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496253,"source":"dbSNP","strand":1,"feature_type":"variation","end":140496253,"alleles":["C","A"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496255,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140496255,"clinical_significance":[],"id":"rs1394985467","seq_region_name":"7"},{"source":"dbSNP","start":140496256,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140496256,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1295647096"},{"seq_region_name":"7","id":"rs1366694069","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C","G","T"],"end":140496263,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496263,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1226095234","feature_type":"variation","strand":1,"end":140496264,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496264},{"clinical_significance":[],"seq_region_name":"7","id":"rs1323147982","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496265,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140496265},{"seq_region_name":"7","id":"rs1273752732","clinical_significance":[],"alleles":["C","A","T"],"end":140496267,"strand":1,"feature_type":"variation","start":140496267,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1348399842","source":"dbSNP","start":140496268,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140496268,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496274,"source":"dbSNP","strand":1,"feature_type":"variation","end":140496274,"alleles":["T","G"],"seq_region_name":"7","id":"rs1211973577","clinical_significance":[]},{"seq_region_name":"7","id":"rs1342951146","clinical_significance":[],"start":140496274,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140496279,"alleles":["TTTTTT","TTTTT","TTTTTTT"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140496275,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140496275,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585519183"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1414535422","source":"dbSNP","start":140496276,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140496276,"alleles":["T","G"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496277,"feature_type":"variation","strand":1,"end":140496277,"alleles":["T","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs546819709"},{"start":140496280,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140496280,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs1795452537","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496281,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140496281,"clinical_significance":[],"seq_region_name":"7","id":"rs1795452560"},{"source":"dbSNP","start":140496288,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140496288,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795452581"},{"source":"dbSNP","start":140496289,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","-"],"end":140496289,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1482388029"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140496290,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496290,"clinical_significance":[],"id":"rs571674994","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140496294,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496294,"source":"dbSNP","seq_region_name":"7","id":"rs1795452663","clinical_significance":[]},{"id":"rs1563105595","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140496296,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496296,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795452714","clinical_significance":[],"end":140496307,"alleles":["CC","C"],"strand":1,"feature_type":"variation","start":140496306,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1248367173","source":"dbSNP","start":140496307,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140496307,"alleles":["C","T"],"feature_type":"variation","strand":1},{"alleles":["G","A"],"end":140496308,"strand":1,"feature_type":"variation","start":140496308,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1248753975","clinical_significance":[]},{"end":140496312,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140496312,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1451331652"},{"seq_region_name":"7","id":"rs1795452862","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496314,"source":"dbSNP","strand":1,"feature_type":"variation","end":140496314,"alleles":["G","C"]},{"seq_region_name":"7","id":"rs1187239474","clinical_significance":[],"alleles":["C","T"],"end":140496316,"strand":1,"feature_type":"variation","start":140496316,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["A","G"],"end":140496317,"strand":1,"feature_type":"variation","start":140496317,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795452934","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1241416336","source":"dbSNP","start":140496318,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140496318,"alleles":["G","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1210994900","source":"dbSNP","start":140496319,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140496319,"alleles":["G","A"],"feature_type":"variation","strand":1},{"id":"rs979848220","seq_region_name":"7","clinical_significance":[],"alleles":["A","G","T"],"end":140496320,"strand":1,"feature_type":"variation","start":140496320,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140496322,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140496322,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1027938109","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs538774481","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496327,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140496327},{"clinical_significance":[],"seq_region_name":"7","id":"rs1415468754","source":"dbSNP","start":140496328,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140496328,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1300214304","alleles":["T","G"],"end":140496330,"feature_type":"variation","strand":1,"source":"dbSNP","start":140496330,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1178648234","clinical_significance":[],"start":140496331,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140496331,"alleles":["C","A","T"],"strand":1,"feature_type":"variation"},{"id":"rs1795453377","seq_region_name":"7","clinical_significance":[],"end":140496334,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140496334,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795453399","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496340,"feature_type":"variation","strand":1,"end":140496340,"alleles":["T","C"]},{"source":"dbSNP","start":140496341,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140496341,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1303918066","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1448136115","seq_region_name":"7","source":"dbSNP","start":140496342,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140496342,"alleles":["G","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795453476","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496347,"source":"dbSNP","strand":1,"feature_type":"variation","end":140496347,"alleles":["C","G"]},{"source":"dbSNP","start":140496350,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140496350,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1360321776","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795453523","end":140496353,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140496353,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1357115967","clinical_significance":[],"start":140496367,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C","G"],"end":140496367,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140496369,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140496369,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130414326"},{"seq_region_name":"7","id":"rs1795453590","clinical_significance":[],"alleles":["G","T"],"end":140496371,"strand":1,"feature_type":"variation","start":140496371,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs28521710","alleles":["C","T"],"end":140496372,"feature_type":"variation","strand":1,"source":"dbSNP","start":140496372,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140496381,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140496381,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1433659929"},{"seq_region_name":"7","id":"rs199728275","clinical_significance":[],"alleles":["CAG","CAGCAG"],"end":140496383,"strand":1,"feature_type":"variation","start":140496381,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs550829687","clinical_significance":[],"end":140496382,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140496382,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1465263657","clinical_significance":[],"start":140496385,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140496385,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140496386,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140496386,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1320733309","seq_region_name":"7"},{"source":"dbSNP","start":140496391,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140496391,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1170297352","seq_region_name":"7"},{"id":"rs1390221933","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140496394,"strand":1,"feature_type":"variation","start":140496394,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1418788169","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496399,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140496399},{"source":"dbSNP","start":140496400,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140496400,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795453853"},{"source":"dbSNP","start":140496401,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A","C"],"end":140496401,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1432247694"},{"id":"rs1296876965","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140496402,"strand":1,"feature_type":"variation","start":140496402,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs983799609","clinical_significance":[],"strand":1,"feature_type":"variation","end":140496404,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496404,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795453958","clinical_significance":[],"end":140496406,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140496406,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140496413,"alleles":["A","C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140496413,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585519247"},{"clinical_significance":[],"id":"rs1795454031","seq_region_name":"7","feature_type":"variation","strand":1,"end":140496414,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496414},{"feature_type":"variation","strand":1,"end":140496421,"alleles":["TTTTTTTT","TTTTTT","TTTTTTT","TTTTTTTTT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496414,"clinical_significance":[],"seq_region_name":"7","id":"rs535847392"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496415,"feature_type":"variation","strand":1,"end":140496415,"alleles":["T","G"],"clinical_significance":[],"id":"rs1220790526","seq_region_name":"7"},{"end":140496421,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140496421,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795454153","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140496430,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140496430,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs367558188"},{"id":"rs1298956991","seq_region_name":"7","clinical_significance":[],"alleles":["A","T"],"end":140496431,"strand":1,"feature_type":"variation","start":140496431,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["C","T"],"end":140496432,"feature_type":"variation","strand":1,"source":"dbSNP","start":140496432,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130414396"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496434,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140496434,"id":"rs557298964","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs976060589","clinical_significance":[],"strand":1,"feature_type":"variation","end":140496436,"alleles":["A","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496436,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1209680908","feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140496437,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496437},{"seq_region_name":"7","id":"rs1307217557","clinical_significance":[],"alleles":["TCT","T"],"end":140496440,"strand":1,"feature_type":"variation","start":140496438,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1268936243","clinical_significance":[],"strand":1,"feature_type":"variation","end":140496439,"alleles":["C","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496439,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496439,"feature_type":"variation","strand":1,"end":140496439,"alleles":["C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795454393"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1466353812","end":140496440,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140496440,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["TTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTT","TTTTTTTTTTTTTT","TTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTT"],"end":140496457,"feature_type":"variation","strand":1,"source":"dbSNP","start":140496440,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs57891726"},{"start":140496441,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140496441,"alleles":["T","C","G"],"strand":1,"feature_type":"variation","id":"rs1585519296","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496447,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140496447,"seq_region_name":"7","id":"rs1309459572","clinical_significance":[]},{"seq_region_name":"7","id":"rs1247991601","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140496449,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496449,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130414454","end":140496451,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140496451,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140496452,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496452,"clinical_significance":[],"seq_region_name":"7","id":"rs1795454706"},{"id":"rs1193378087","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140496458,"alleles":["TTTTTA","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496453,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795454767","feature_type":"variation","strand":1,"end":140496454,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496454},{"clinical_significance":[],"seq_region_name":"7","id":"rs1423512853","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496454,"feature_type":"variation","strand":1,"end":140496458,"alleles":["TTTTA","-"]},{"strand":1,"feature_type":"variation","end":140496455,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496455,"source":"dbSNP","id":"rs202203878","seq_region_name":"7","clinical_significance":[]},{"id":"rs1432907038","seq_region_name":"7","clinical_significance":[],"start":140496455,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140496458,"alleles":["TTTA","-"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1795454925","seq_region_name":"7","feature_type":"variation","strand":1,"end":140496455,"alleles":["-","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496456},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496456,"source":"dbSNP","strand":1,"feature_type":"variation","end":140496456,"alleles":["T","A","G"],"seq_region_name":"7","id":"rs200302713","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs199717075","source":"dbSNP","start":140496456,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TTA","-"],"end":140496458,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496456,"feature_type":"variation","strand":1,"end":140496459,"alleles":["TTAG","GAT"],"clinical_significance":[],"id":"rs796568281","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs58616035","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496457,"feature_type":"variation","strand":1,"alleles":["T","A","G"],"end":140496457},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496457,"feature_type":"variation","strand":1,"alleles":["TA","-"],"end":140496458,"clinical_significance":[],"seq_region_name":"7","id":"rs1563105644"},{"end":140496459,"alleles":["TAG","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140496457,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs200769100","seq_region_name":"7"},{"start":140496458,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140496457,"alleles":["-","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1563105652","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496458,"feature_type":"variation","strand":1,"alleles":["A","-"],"end":140496458,"clinical_significance":[],"id":"rs1425439003","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795455266","clinical_significance":[],"alleles":["A","T"],"end":140496458,"strand":1,"feature_type":"variation","start":140496458,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140496458,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140496460,"alleles":["AGA","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1563105657","clinical_significance":[]},{"alleles":["AGA","-"],"end":140496460,"strand":1,"feature_type":"variation","start":140496458,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1563105659","clinical_significance":[]},{"source":"dbSNP","start":140496458,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140496465,"alleles":["AGATAGAG","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1563105661","seq_region_name":"7"},{"id":"rs60075764","seq_region_name":"7","clinical_significance":[],"start":140496459,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140496459,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"start":140496460,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140496462,"alleles":["ATA","ATATA"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs765485030","clinical_significance":[]},{"id":"rs1563105665","seq_region_name":"7","clinical_significance":[],"start":140496463,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140496462,"alleles":["-","TC","TG","TT"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1455227090","feature_type":"variation","strand":1,"end":140496463,"alleles":["G","C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496463},{"seq_region_name":"7","id":"rs1795455615","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140496469,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496469,"source":"dbSNP"},{"start":140496470,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140496470,"alleles":["A","C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1349910057","clinical_significance":[]},{"source":"dbSNP","start":140496473,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140496473,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795455689"},{"clinical_significance":[],"id":"rs1472949241","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496477,"feature_type":"variation","strand":1,"end":140496477,"alleles":["C","G"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496478,"source":"dbSNP","strand":1,"feature_type":"variation","end":140496478,"alleles":["A","T"],"seq_region_name":"7","id":"rs2130414547","clinical_significance":[]},{"end":140496480,"alleles":["C","A","G"],"strand":1,"feature_type":"variation","start":140496480,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1254255332","clinical_significance":[]},{"seq_region_name":"7","id":"rs1194228414","clinical_significance":[],"end":140496482,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140496482,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140496483,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140496483,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1480527578"},{"end":140496493,"alleles":["GCTGAAGTGC","GC"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140496484,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795455827","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140496493,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496493,"source":"dbSNP","seq_region_name":"7","id":"rs1438556862","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140496495,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496495,"clinical_significance":[],"id":"rs1320482320","seq_region_name":"7"},{"end":140496496,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140496496,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585519347"},{"id":"rs1232213300","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140496501,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496501,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140496503,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496503,"source":"dbSNP","seq_region_name":"7","id":"rs1317503569","clinical_significance":[]},{"seq_region_name":"7","id":"rs1350507983","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496508,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140496508},{"seq_region_name":"7","id":"rs189535137","clinical_significance":[],"alleles":["C","T"],"end":140496514,"strand":1,"feature_type":"variation","start":140496514,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795456071","clinical_significance":[],"start":140496517,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140496517,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140496520,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496520,"clinical_significance":[],"seq_region_name":"7","id":"rs1795456104"},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140496522,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496522,"source":"dbSNP","seq_region_name":"7","id":"rs1795456128","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496525,"source":"dbSNP","strand":1,"feature_type":"variation","end":140496525,"alleles":["A","C","G"],"seq_region_name":"7","id":"rs1289841691","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585519363","clinical_significance":[],"end":140496526,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140496526,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140496529,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140496529,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1389283783"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496533,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140496533,"seq_region_name":"7","id":"rs1795456227","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140496571,"alleles":["TCAAGCAATTCTCCTGCCTCAGCCTCCTGAGTAGCT","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496536,"source":"dbSNP","id":"rs1795456243","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1291641384","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496542,"source":"dbSNP","strand":1,"feature_type":"variation","end":140496542,"alleles":["A","G"]},{"clinical_significance":[],"id":"rs1366659597","seq_region_name":"7","source":"dbSNP","start":140496548,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140496548,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795456344","clinical_significance":[],"start":140496551,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140496551,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1395537753","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496552,"feature_type":"variation","strand":1,"end":140496552,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795456393","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496553,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140496553},{"end":140496558,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140496558,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795456430"},{"alleles":["T","A","C"],"end":140496563,"feature_type":"variation","strand":1,"source":"dbSNP","start":140496563,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1293947617"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795456479","feature_type":"variation","strand":1,"end":140496564,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496564},{"seq_region_name":"7","id":"rs1459224588","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140496569,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496569,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1795456517","seq_region_name":"7","alleles":["C","G"],"end":140496570,"feature_type":"variation","strand":1,"source":"dbSNP","start":140496570,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs921895187","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140496574,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496574},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496576,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140496576,"seq_region_name":"7","id":"rs1795456565","clinical_significance":[]},{"seq_region_name":"7","id":"rs1228761597","clinical_significance":[],"start":140496579,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140496579,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs866173031","clinical_significance":[],"end":140496582,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140496582,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1457837358","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140496583,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496583,"source":"dbSNP"},{"source":"dbSNP","start":140496584,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140496583,"alleles":["-","ACAT"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795456680","seq_region_name":"7"},{"alleles":["G","A"],"end":140496584,"strand":1,"feature_type":"variation","start":140496584,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs573202420","clinical_significance":[]},{"id":"rs57352707","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496585,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140496585},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496586,"source":"dbSNP","strand":1,"feature_type":"variation","end":140496586,"alleles":["C","A","T"],"id":"rs1795456760","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","C","G","T"],"end":140496587,"strand":1,"feature_type":"variation","start":140496587,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs13311547","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140496588,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496588,"source":"dbSNP","seq_region_name":"7","id":"rs1226704983","clinical_significance":[]},{"id":"rs1795456919","seq_region_name":"7","clinical_significance":[],"alleles":["CC","C"],"end":140496590,"strand":1,"feature_type":"variation","start":140496589,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1795456942","seq_region_name":"7","alleles":["A","G"],"end":140496594,"feature_type":"variation","strand":1,"source":"dbSNP","start":140496594,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140496595,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140496595,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs181507570"},{"strand":1,"feature_type":"variation","end":140496599,"alleles":["CACCT","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496595,"source":"dbSNP","id":"rs1795457007","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","T"],"end":140496597,"feature_type":"variation","strand":1,"source":"dbSNP","start":140496597,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795457034","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795457056","clinical_significance":[],"start":140496601,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140496601,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1209834267","feature_type":"variation","strand":1,"alleles":["TTTTGTATATTTT","TTTT"],"end":140496619,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496607},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496611,"source":"dbSNP","strand":1,"feature_type":"variation","end":140496611,"alleles":["G","A","T"],"seq_region_name":"7","id":"rs1227540442","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1452185007","feature_type":"variation","strand":1,"end":140496612,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496612},{"seq_region_name":"7","id":"rs201462482","clinical_significance":[],"start":140496612,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TATAT","TAT"],"end":140496616,"strand":1,"feature_type":"variation"},{"start":140496613,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","-"],"end":140496613,"strand":1,"feature_type":"variation","id":"rs1795457241","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795457279","clinical_significance":[],"end":140496614,"alleles":["T","TT"],"strand":1,"feature_type":"variation","start":140496614,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140496617,"alleles":["TATT","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496614,"clinical_significance":[],"seq_region_name":"7","id":"rs1224448539"},{"clinical_significance":[],"seq_region_name":"7","id":"rs28652588","end":140496615,"alleles":["A","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140496615,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs56796233","seq_region_name":"7","clinical_significance":[],"alleles":["A","-"],"end":140496615,"strand":1,"feature_type":"variation","start":140496615,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs764567620","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","AA"],"end":140496615,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496615,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795457603","clinical_significance":[],"alleles":["TTTTTTTTTT","TTTTTTTTT"],"end":140496625,"strand":1,"feature_type":"variation","start":140496616,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1301541947","clinical_significance":[],"end":140496617,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140496617,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140496621,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496621,"clinical_significance":[],"id":"rs1388306953","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1368427035","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496625,"feature_type":"variation","strand":1,"end":140496625,"alleles":["T","C"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496627,"source":"dbSNP","strand":1,"feature_type":"variation","end":140496627,"alleles":["G","C"],"seq_region_name":"7","id":"rs1795457709","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795457738","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140496630,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496630},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795457763","source":"dbSNP","start":140496632,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140496632,"alleles":["G","C"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140496633,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496633,"clinical_significance":[],"seq_region_name":"7","id":"rs1325171385"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496634,"source":"dbSNP","strand":1,"feature_type":"variation","end":140496634,"alleles":["C","T"],"seq_region_name":"7","id":"rs186459138","clinical_significance":[]},{"seq_region_name":"7","id":"rs190101122","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496635,"source":"dbSNP","strand":1,"feature_type":"variation","end":140496635,"alleles":["G","A","T"]},{"feature_type":"variation","strand":1,"end":140496638,"alleles":["GGGG","GGGGG"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496635,"clinical_significance":[],"seq_region_name":"7","id":"rs1563105697"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1413785957","source":"dbSNP","start":140496638,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140496638,"alleles":["G","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs571024663","clinical_significance":[],"start":140496639,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140496639,"strand":1,"feature_type":"variation"},{"id":"rs2130414754","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496642,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140496642},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496643,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140496643,"clinical_significance":[],"id":"rs1157910237","seq_region_name":"7"},{"alleles":["C","T"],"end":140496644,"strand":1,"feature_type":"variation","start":140496644,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795458051","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140496646,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496646,"clinical_significance":[],"seq_region_name":"7","id":"rs1795458078"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496647,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140496647,"seq_region_name":"7","id":"rs1795458113","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs181625252","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140496648,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496648},{"seq_region_name":"7","id":"rs1795458179","clinical_significance":[],"end":140496651,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140496651,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795458218","feature_type":"variation","strand":1,"end":140496652,"alleles":["A","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496652},{"clinical_significance":[],"id":"rs1585519433","seq_region_name":"7","source":"dbSNP","start":140496655,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140496655,"alleles":["A","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795458279","clinical_significance":[],"start":140496657,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140496657,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795458303","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496660,"feature_type":"variation","strand":1,"end":140496660,"alleles":["G","A","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1452969219","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496665,"feature_type":"variation","strand":1,"end":140496665,"alleles":["C","T"]},{"id":"rs1252719849","seq_region_name":"7","clinical_significance":[],"end":140496666,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140496666,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1189802812","feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140496668,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496668},{"id":"rs1466679208","seq_region_name":"7","clinical_significance":[],"end":140496669,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140496669,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140496677,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140496677,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs2130414797","seq_region_name":"7"},{"start":140496679,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140496679,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585519440","clinical_significance":[]},{"seq_region_name":"7","id":"rs1260225344","clinical_significance":[],"start":140496680,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140496680,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1202925404","source":"dbSNP","start":140496681,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140496681,"alleles":["T","C"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496684,"feature_type":"variation","strand":1,"end":140496684,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs186286899"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585519444","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496687,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140496687},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496690,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140496690,"clinical_significance":[],"id":"rs1410249241","seq_region_name":"7"},{"alleles":["G","A"],"end":140496691,"feature_type":"variation","strand":1,"source":"dbSNP","start":140496691,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795458666"},{"source":"dbSNP","start":140496693,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140496693,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585519447"},{"seq_region_name":"7","id":"rs1795458720","clinical_significance":[],"alleles":["C","T"],"end":140496695,"strand":1,"feature_type":"variation","start":140496695,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1585519449","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496696,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140496696},{"alleles":["C","T"],"end":140496698,"strand":1,"feature_type":"variation","start":140496698,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795458782","clinical_significance":[]},{"seq_region_name":"7","id":"rs1309595519","clinical_significance":[],"end":140496703,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140496703,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140496704,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496704,"source":"dbSNP","seq_region_name":"7","id":"rs1795458847","clinical_significance":[]},{"source":"dbSNP","start":140496707,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140496707,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795458875"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496708,"feature_type":"variation","strand":1,"end":140496708,"alleles":["T","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1348341647"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1408266528","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496709,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140496709},{"seq_region_name":"7","id":"rs2130414839","clinical_significance":[],"alleles":["CTGGGATTAC","-"],"end":140496719,"strand":1,"feature_type":"variation","start":140496710,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1279127088","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140496713,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496713},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140496714,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496714,"clinical_significance":[],"seq_region_name":"7","id":"rs1656008485"},{"strand":1,"feature_type":"variation","end":140496721,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496721,"source":"dbSNP","seq_region_name":"7","id":"rs888031688","clinical_significance":[]},{"seq_region_name":"7","id":"rs1005103991","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140496723,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496723,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496724,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140496724,"clinical_significance":[],"seq_region_name":"7","id":"rs1288400411"},{"clinical_significance":[],"id":"rs1359324412","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140496725,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496725},{"alleles":["G","A"],"end":140496726,"feature_type":"variation","strand":1,"source":"dbSNP","start":140496726,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1316128195"},{"id":"rs1381727145","seq_region_name":"7","clinical_significance":[],"alleles":["A","C"],"end":140496731,"strand":1,"feature_type":"variation","start":140496731,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["C","T"],"end":140496732,"strand":1,"feature_type":"variation","start":140496732,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1014610889","clinical_significance":[]},{"seq_region_name":"7","id":"rs965676135","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496735,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140496735},{"seq_region_name":"7","id":"rs376959209","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496738,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","G"],"end":140496738},{"clinical_significance":[],"id":"rs1795459283","seq_region_name":"7","source":"dbSNP","start":140496739,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140496739,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs191208364","source":"dbSNP","start":140496743,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140496743,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1433047952","clinical_significance":[],"start":140496744,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140496744,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496745,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140496745,"seq_region_name":"7","id":"rs896744023","clinical_significance":[]},{"seq_region_name":"7","id":"rs1013806330","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496746,"source":"dbSNP","strand":1,"feature_type":"variation","end":140496746,"alleles":["A","T"]},{"id":"rs1795459427","seq_region_name":"7","clinical_significance":[],"end":140496748,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140496748,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140496750,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140496750,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795459456"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1028768959","feature_type":"variation","strand":1,"end":140496751,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496751},{"feature_type":"variation","strand":1,"end":140496752,"alleles":["T","A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496752,"clinical_significance":[],"id":"rs1795459500","seq_region_name":"7"},{"seq_region_name":"7","id":"rs953238120","clinical_significance":[],"end":140496753,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140496753,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496757,"source":"dbSNP","strand":1,"feature_type":"variation","end":140496757,"alleles":["T","A"],"seq_region_name":"7","id":"rs1795459545","clinical_significance":[]},{"alleles":["G","A","C"],"end":140496767,"strand":1,"feature_type":"variation","start":140496767,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs542941556","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496770,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140496770,"seq_region_name":"7","id":"rs1795459605","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795459625","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496779,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140496779},{"seq_region_name":"7","id":"rs1445943974","clinical_significance":[],"strand":1,"feature_type":"variation","end":140496784,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496784,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1256197531","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496786,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140496786},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496787,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140496787,"seq_region_name":"7","id":"rs914368799","clinical_significance":[]},{"seq_region_name":"7","id":"rs1484515034","clinical_significance":[],"start":140496788,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140496788,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140496792,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140496792,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585519492"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1279146676","feature_type":"variation","strand":1,"end":140496794,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496794},{"start":140496797,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","G"],"end":140496797,"strand":1,"feature_type":"variation","id":"rs1181019690","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140496802,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496802,"clinical_significance":[],"id":"rs945977675","seq_region_name":"7"},{"clinical_significance":[],"id":"rs977282329","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496804,"feature_type":"variation","strand":1,"end":140496804,"alleles":["T","C"]},{"alleles":["A","G"],"end":140496818,"feature_type":"variation","strand":1,"source":"dbSNP","start":140496818,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1228956715"},{"end":140496821,"alleles":["G","C","T"],"strand":1,"feature_type":"variation","start":140496821,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1341130519","clinical_significance":[]},{"seq_region_name":"7","id":"rs1237680048","clinical_significance":[],"end":140496830,"alleles":["C","A","G"],"strand":1,"feature_type":"variation","start":140496830,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140496837,"alleles":["T","A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496837,"clinical_significance":[],"seq_region_name":"7","id":"rs1341176389"},{"id":"rs1795460034","seq_region_name":"7","clinical_significance":[],"alleles":["A","C"],"end":140496845,"strand":1,"feature_type":"variation","start":140496845,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140496847,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140496847,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1295241824","clinical_significance":[]},{"clinical_significance":[],"id":"rs1412987806","seq_region_name":"7","alleles":["A","G"],"end":140496848,"feature_type":"variation","strand":1,"source":"dbSNP","start":140496848,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496849,"source":"dbSNP","strand":1,"feature_type":"variation","end":140496849,"alleles":["A","C","G"],"seq_region_name":"7","id":"rs1795460106","clinical_significance":[]},{"id":"rs1473530214","seq_region_name":"7","clinical_significance":[],"alleles":["AGAAAGA","AGA"],"end":140496861,"strand":1,"feature_type":"variation","start":140496855,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496857,"feature_type":"variation","strand":1,"alleles":["AAA","AA"],"end":140496859,"clinical_significance":[],"seq_region_name":"7","id":"rs1795460165"},{"alleles":["A","T"],"end":140496859,"strand":1,"feature_type":"variation","start":140496859,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795460187","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs182250884","alleles":["A","T"],"end":140496861,"feature_type":"variation","strand":1,"source":"dbSNP","start":140496861,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140496864,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140496864,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795460249"},{"clinical_significance":[],"id":"rs1795460279","seq_region_name":"7","feature_type":"variation","strand":1,"end":140496881,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496881},{"clinical_significance":[],"seq_region_name":"7","id":"rs1308855776","alleles":["T","A","C"],"end":140496884,"feature_type":"variation","strand":1,"source":"dbSNP","start":140496884,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140496890,"alleles":["AAAAAA","AAAAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140496885,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1413040140"},{"alleles":["A","G"],"end":140496890,"feature_type":"variation","strand":1,"source":"dbSNP","start":140496890,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795460374"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1430357950","source":"dbSNP","start":140496891,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140496891,"alleles":["T","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795460417","end":140496893,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140496893,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496894,"source":"dbSNP","strand":1,"feature_type":"variation","end":140496894,"alleles":["A","G"],"seq_region_name":"7","id":"rs939391545","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140496895,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496895,"clinical_significance":[],"seq_region_name":"7","id":"rs1001316682"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496899,"feature_type":"variation","strand":1,"end":140496899,"alleles":["G","A"],"clinical_significance":[],"id":"rs1795460498","seq_region_name":"7"},{"clinical_significance":[],"id":"rs750674964","seq_region_name":"7","feature_type":"variation","strand":1,"end":140496901,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496901},{"seq_region_name":"7","id":"rs1795460540","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496909,"source":"dbSNP","strand":1,"feature_type":"variation","end":140496909,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs1795460574","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496914,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140496914},{"seq_region_name":"7","id":"rs1795460585","clinical_significance":[],"start":140496914,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140496914,"alleles":["G","-"],"strand":1,"feature_type":"variation"},{"alleles":["TTCGGCAAATT","T"],"end":140496925,"feature_type":"variation","strand":1,"source":"dbSNP","start":140496915,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs2130415017","seq_region_name":"7"},{"id":"rs1795460609","seq_region_name":"7","clinical_significance":[],"end":140496916,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140496916,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1170368692","clinical_significance":[],"start":140496917,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140496917,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs149686942","clinical_significance":[],"start":140496918,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140496918,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"alleles":["A","G"],"end":140496922,"feature_type":"variation","strand":1,"source":"dbSNP","start":140496922,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795460691"},{"clinical_significance":[],"seq_region_name":"7","id":"rs895267726","source":"dbSNP","start":140496926,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140496926,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140496928,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496928,"clinical_significance":[],"seq_region_name":"7","id":"rs1189518412"},{"seq_region_name":"7","id":"rs1795460749","clinical_significance":[],"start":140496930,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140496930,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1473937744","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496935,"feature_type":"variation","strand":1,"end":140496935,"alleles":["A","G"]},{"id":"rs951860829","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496940,"source":"dbSNP","strand":1,"feature_type":"variation","end":140496940,"alleles":["C","T"]},{"feature_type":"variation","strand":1,"end":140496944,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496944,"clinical_significance":[],"seq_region_name":"7","id":"rs1205355651"},{"clinical_significance":[],"seq_region_name":"7","id":"rs948094833","source":"dbSNP","start":140496945,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140496945,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["GTCTGT","GTCTGTCTGT"],"end":140496950,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496945,"clinical_significance":[],"seq_region_name":"7","id":"rs1795460899"},{"start":140496946,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140496946,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1015134497","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795460941","end":140496952,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140496952,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs373947553","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496956,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140496956},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140496958,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496958,"source":"dbSNP","seq_region_name":"7","id":"rs1049264764","clinical_significance":[]},{"start":140496959,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140496959,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795461006","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140496961,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496961,"clinical_significance":[],"seq_region_name":"7","id":"rs1795461030"},{"id":"rs1795461052","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496963,"source":"dbSNP","strand":1,"feature_type":"variation","end":140496963,"alleles":["T","G"]},{"start":140496968,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140496968,"alleles":["A","G"],"strand":1,"feature_type":"variation","id":"rs1357022943","seq_region_name":"7","clinical_significance":[]},{"id":"rs1428853362","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140496969,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496969,"source":"dbSNP"},{"alleles":["G","A"],"end":140496970,"strand":1,"feature_type":"variation","start":140496970,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs975968825","seq_region_name":"7","clinical_significance":[]},{"end":140496971,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140496971,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs546742746"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1005156249","feature_type":"variation","strand":1,"end":140496972,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140496972},{"strand":1,"feature_type":"variation","end":140496975,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496975,"source":"dbSNP","id":"rs1795461233","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585519543","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496977,"source":"dbSNP","strand":1,"feature_type":"variation","end":140496977,"alleles":["T","G"]},{"strand":1,"feature_type":"variation","end":140496979,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496979,"source":"dbSNP","seq_region_name":"7","id":"rs1015206600","clinical_significance":[]},{"source":"dbSNP","start":140496981,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140496981,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1450359932","seq_region_name":"7"},{"end":140496982,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140496982,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs925405309","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140496983,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496983,"source":"dbSNP","id":"rs564957355","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140496984,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140496984,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs111463773"},{"alleles":["A","C"],"end":140496987,"strand":1,"feature_type":"variation","start":140496987,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs550832348","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496989,"source":"dbSNP","strand":1,"feature_type":"variation","end":140496989,"alleles":["C","A","T"],"id":"rs61638073","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs918088157","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140496997,"source":"dbSNP","strand":1,"feature_type":"variation","end":140496997,"alleles":["A","G"]},{"strand":1,"feature_type":"variation","end":140497001,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497001,"source":"dbSNP","seq_region_name":"7","id":"rs949652970","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130415136","clinical_significance":[],"end":140497002,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140497002,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs59517838","clinical_significance":[],"strand":1,"feature_type":"variation","end":140497005,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497005,"source":"dbSNP"},{"seq_region_name":"7","id":"rs60819576","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497007,"source":"dbSNP","strand":1,"feature_type":"variation","end":140497007,"alleles":["A","G"]},{"alleles":["G","A"],"end":140497012,"strand":1,"feature_type":"variation","start":140497012,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795461578","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs568369751","feature_type":"variation","strand":1,"end":140497013,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497013},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497018,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140497018,"clinical_significance":[],"id":"rs58064262","seq_region_name":"7"},{"clinical_significance":[],"id":"rs953161040","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497022,"feature_type":"variation","strand":1,"end":140497022,"alleles":["C","A"]},{"id":"rs1230793880","seq_region_name":"7","clinical_significance":[],"alleles":["A","G"],"end":140497023,"strand":1,"feature_type":"variation","start":140497023,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795461691","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["ATA","A"],"end":140497025,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497023,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497024,"source":"dbSNP","strand":1,"feature_type":"variation","end":140497024,"alleles":["T","C"],"seq_region_name":"7","id":"rs1795461712","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140497025,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497025,"source":"dbSNP","seq_region_name":"7","id":"rs58960936","clinical_significance":[]},{"start":140497028,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140497028,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs1795461756","seq_region_name":"7","clinical_significance":[]},{"id":"rs1795461779","seq_region_name":"7","clinical_significance":[],"start":140497031,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140497031,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs905553816","clinical_significance":[],"start":140497034,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140497034,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795461825","end":140497035,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140497035,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs57527067","clinical_significance":[],"start":140497036,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140497036,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"end":140497043,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140497043,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1340552094","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1011710307","alleles":["A","G"],"end":140497053,"feature_type":"variation","strand":1,"source":"dbSNP","start":140497053,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1001229451","seq_region_name":"7","end":140497057,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140497057,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1049173588","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497059,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140497059},{"end":140497061,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140497061,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795462082"},{"alleles":["C","T"],"end":140497062,"strand":1,"feature_type":"variation","start":140497062,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795462116","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1021428563","end":140497064,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140497064,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497066,"feature_type":"variation","strand":1,"end":140497066,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1348884545"},{"alleles":["C","G","T"],"end":140497067,"strand":1,"feature_type":"variation","start":140497067,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs61407649","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140497068,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497068,"clinical_significance":[],"seq_region_name":"7","id":"rs967160750"},{"clinical_significance":[],"id":"rs887539950","seq_region_name":"7","feature_type":"variation","strand":1,"end":140497070,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497070},{"id":"rs2130415221","seq_region_name":"7","clinical_significance":[],"start":140497071,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140497071,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497073,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140497073,"clinical_significance":[],"id":"rs186211566","seq_region_name":"7"},{"seq_region_name":"7","id":"rs548184307","clinical_significance":[],"start":140497074,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140497074,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs928585777","feature_type":"variation","strand":1,"end":140497075,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497075},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497076,"feature_type":"variation","strand":1,"end":140497076,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs58156882"},{"seq_region_name":"7","id":"rs965841432","clinical_significance":[],"end":140497077,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140497077,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140497081,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140497081,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs997416483"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497082,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140497082,"clinical_significance":[],"id":"rs1795462452","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140497083,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497083,"clinical_significance":[],"seq_region_name":"7","id":"rs1795462483"},{"source":"dbSNP","start":140497084,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140497084,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs960222329"},{"seq_region_name":"7","id":"rs1388245308","clinical_significance":[],"start":140497084,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140497085,"alleles":["AA","AAA"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795462563","source":"dbSNP","start":140497085,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140497085,"alleles":["A","G"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140497089,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497089,"source":"dbSNP","seq_region_name":"7","id":"rs1795462586","clinical_significance":[]},{"end":140497091,"alleles":["G","A","C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140497091,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs7812236"},{"source":"dbSNP","start":140497091,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140497091,"alleles":["G","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1554453903"},{"clinical_significance":[],"seq_region_name":"7","id":"rs386718473","alleles":["GC","AT"],"end":140497092,"feature_type":"variation","strand":1,"source":"dbSNP","start":140497091,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs879526934","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497091,"feature_type":"variation","strand":1,"end":140497092,"alleles":["GC","A","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs10262827","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140497092,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497092},{"seq_region_name":"7","id":"rs1554453902","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497092,"source":"dbSNP","strand":1,"feature_type":"variation","end":140497092,"alleles":["C","-"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497096,"source":"dbSNP","strand":1,"feature_type":"variation","end":140497096,"alleles":["C","G","T"],"seq_region_name":"7","id":"rs948175364","clinical_significance":[]},{"source":"dbSNP","start":140497098,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140497098,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1049150246"},{"seq_region_name":"7","id":"rs59714080","clinical_significance":[],"end":140497099,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140497099,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497103,"source":"dbSNP","strand":1,"feature_type":"variation","end":140497103,"alleles":["A","G"],"seq_region_name":"7","id":"rs57449845","clinical_significance":[]},{"seq_region_name":"7","id":"rs1191485332","clinical_significance":[],"strand":1,"feature_type":"variation","end":140497105,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497105,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140497109,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497109,"source":"dbSNP","seq_region_name":"7","id":"rs1416415111","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795463052","alleles":["G","A"],"end":140497113,"feature_type":"variation","strand":1,"source":"dbSNP","start":140497113,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497114,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140497114,"clinical_significance":[],"seq_region_name":"7","id":"rs1248556962"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795463101","source":"dbSNP","start":140497120,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140497120,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs940866342","feature_type":"variation","strand":1,"end":140497127,"alleles":["A","C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497127},{"seq_region_name":"7","id":"rs1795463158","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497128,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140497128},{"source":"dbSNP","start":140497129,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140497129,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795463185"},{"clinical_significance":[],"seq_region_name":"7","id":"rs925236426","end":140497130,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140497130,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1283842488","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140497132,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497132},{"clinical_significance":[],"id":"rs779960159","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140497134,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497134},{"start":140497135,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140497135,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1219987030","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585519676","feature_type":"variation","strand":1,"end":140497136,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497136},{"strand":1,"feature_type":"variation","alleles":["T","A","C","G"],"end":140497137,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497137,"source":"dbSNP","id":"rs7802244","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1405452465","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497139,"feature_type":"variation","strand":1,"end":140497139,"alleles":["A","G","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs577398104","feature_type":"variation","strand":1,"end":140497142,"alleles":["T","C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497142},{"clinical_significance":[],"seq_region_name":"7","id":"rs1291137352","feature_type":"variation","strand":1,"alleles":["A","T"],"end":140497146,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497146},{"end":140497146,"alleles":["A","AA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140497146,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1366631592","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795463526","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497155,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140497155},{"feature_type":"variation","strand":1,"end":140497161,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497161,"clinical_significance":[],"seq_region_name":"7","id":"rs1432290549"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497161,"feature_type":"variation","strand":1,"alleles":["C","-"],"end":140497161,"clinical_significance":[],"seq_region_name":"7","id":"rs1435883821"},{"feature_type":"variation","strand":1,"end":140497162,"alleles":["G","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497162,"clinical_significance":[],"id":"rs1300528361","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795463625","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140497163,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497163,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795463645","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140497164,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497164,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1795463681","seq_region_name":"7","end":140497165,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140497165,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140497167,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140497167,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585519690"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497168,"source":"dbSNP","strand":1,"feature_type":"variation","end":140497168,"alleles":["G","A"],"id":"rs988624893","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140497170,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497170,"clinical_significance":[],"seq_region_name":"7","id":"rs1585519693"},{"seq_region_name":"7","id":"rs902130490","clinical_significance":[],"alleles":["C","G"],"end":140497171,"strand":1,"feature_type":"variation","start":140497171,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795463770","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497173,"source":"dbSNP","strand":1,"feature_type":"variation","end":140497173,"alleles":["C","G","T"]},{"id":"rs998139540","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140497174,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497174,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1050105870","clinical_significance":[],"strand":1,"feature_type":"variation","end":140497178,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497178,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140497180,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497180,"clinical_significance":[],"seq_region_name":"7","id":"rs888752684"},{"strand":1,"feature_type":"variation","end":140497181,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497181,"source":"dbSNP","seq_region_name":"7","id":"rs1795463858","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795463879","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["GCGACAAGAGCGA","GCGA"],"end":140497194,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497182,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1011302265","clinical_significance":[],"start":140497183,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140497183,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1275832367","seq_region_name":"7","feature_type":"variation","strand":1,"end":140497184,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497184},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795463937","source":"dbSNP","start":140497184,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","-"],"end":140497184,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140497187,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497187,"source":"dbSNP","seq_region_name":"7","id":"rs1795463960","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs191104108","feature_type":"variation","strand":1,"end":140497192,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497192},{"seq_region_name":"7","id":"rs967088625","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497193,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140497193},{"source":"dbSNP","start":140497198,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140497198,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585519721"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1262108439","feature_type":"variation","strand":1,"end":140497199,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497199},{"alleles":["C","T"],"end":140497200,"feature_type":"variation","strand":1,"source":"dbSNP","start":140497200,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795464090"},{"end":140497202,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140497202,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1241553028","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1484947756","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497202,"feature_type":"variation","strand":1,"alleles":["TCTC","-"],"end":140497205},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795464150","source":"dbSNP","start":140497203,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140497206,"alleles":["CTCA","-"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1210867015","clinical_significance":[],"strand":1,"feature_type":"variation","end":140497207,"alleles":["TCAA","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497204,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1278440462","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497205,"feature_type":"variation","strand":1,"end":140497205,"alleles":["C","A","G"]},{"id":"rs747838376","seq_region_name":"7","clinical_significance":[],"alleles":["CAAA","-"],"end":140497208,"strand":1,"feature_type":"variation","start":140497205,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140497209,"alleles":["CAAAA","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497205,"clinical_significance":[],"seq_region_name":"7","id":"rs763651518"},{"source":"dbSNP","start":140497206,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140497206,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1210023620","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140497223,"alleles":["AAAAAAAAAAAAAAAAAA","AAAAAAAAAAA","AAAAAAAAAAAA","AAAAAAAAAAAAA","AAAAAAAAAAAAAA","AAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497206,"clinical_significance":[],"seq_region_name":"7","id":"rs58743847"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497209,"feature_type":"variation","strand":1,"alleles":["A","C","G","T"],"end":140497209,"clinical_significance":[],"id":"rs949515431","seq_region_name":"7"},{"start":140497212,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140497212,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795464604","clinical_significance":[]},{"alleles":["A","G"],"end":140497215,"feature_type":"variation","strand":1,"source":"dbSNP","start":140497215,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1376972164"},{"start":140497216,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140497216,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1310627059","clinical_significance":[]},{"seq_region_name":"7","id":"rs1199443406","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["AAAAAT","-"],"end":140497224,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497219,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1795464700","seq_region_name":"7","alleles":["AAAAATTCATTCTA","A"],"end":140497232,"feature_type":"variation","strand":1,"source":"dbSNP","start":140497219,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140497220,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497220,"source":"dbSNP","seq_region_name":"7","id":"rs991247363","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497220,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AAAAT","G"],"end":140497224,"seq_region_name":"7","id":"rs796354294","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1379163628","alleles":["AAAATT","-"],"end":140497225,"feature_type":"variation","strand":1,"source":"dbSNP","start":140497220,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1795464781","seq_region_name":"7","clinical_significance":[],"end":140497227,"alleles":["AAAATTCA","A"],"strand":1,"feature_type":"variation","start":140497220,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497221,"source":"dbSNP","strand":1,"feature_type":"variation","end":140497224,"alleles":["AAAT","-"],"seq_region_name":"7","id":"rs761094626","clinical_significance":[]},{"clinical_significance":[],"id":"rs761043898","seq_region_name":"7","alleles":["AAATT","-"],"end":140497225,"feature_type":"variation","strand":1,"source":"dbSNP","start":140497221,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1563105841","seq_region_name":"7","source":"dbSNP","start":140497222,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AAT","-"],"end":140497224,"feature_type":"variation","strand":1},{"start":140497223,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140497223,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs998681339","clinical_significance":[]},{"end":140497224,"alleles":["T","A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140497224,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs10590334"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563105843","source":"dbSNP","start":140497225,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["-","GG"],"end":140497224,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140497226,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["-","GC","GG"],"end":140497225,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1476887818"},{"clinical_significance":[],"id":"rs1426702618","seq_region_name":"7","alleles":["C","G"],"end":140497226,"feature_type":"variation","strand":1,"source":"dbSNP","start":140497226,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1418676680","alleles":["A","G"],"end":140497227,"feature_type":"variation","strand":1,"source":"dbSNP","start":140497227,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795465076","feature_type":"variation","strand":1,"end":140497233,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497233},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795465103","source":"dbSNP","start":140497235,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140497235,"alleles":["C","-"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs2130415581","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497237,"feature_type":"variation","strand":1,"alleles":["GTGT","GTGTGT"],"end":140497240},{"id":"rs1188817812","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140497244,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497244,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140497245,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497245,"clinical_significance":[],"seq_region_name":"7","id":"rs959991088"},{"clinical_significance":[],"id":"rs1187417550","seq_region_name":"7","end":140497257,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140497257,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","T"],"end":140497258,"feature_type":"variation","strand":1,"source":"dbSNP","start":140497258,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs139216881"},{"feature_type":"variation","strand":1,"end":140497261,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497261,"clinical_significance":[],"seq_region_name":"7","id":"rs1795465211"},{"seq_region_name":"7","id":"rs1253401358","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497269,"source":"dbSNP","strand":1,"feature_type":"variation","end":140497269,"alleles":["C","G"]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140497271,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497271,"clinical_significance":[],"seq_region_name":"7","id":"rs1202845029"},{"alleles":["C","T"],"end":140497273,"feature_type":"variation","strand":1,"source":"dbSNP","start":140497273,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs916603089"},{"end":140497274,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140497274,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1291215839"},{"seq_region_name":"7","id":"rs1233374209","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497280,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140497280},{"seq_region_name":"7","id":"rs1795465368","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497286,"source":"dbSNP","strand":1,"feature_type":"variation","end":140497286,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs183165209","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497288,"source":"dbSNP","strand":1,"feature_type":"variation","end":140497288,"alleles":["C","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497289,"feature_type":"variation","strand":1,"end":140497289,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1291082050"},{"source":"dbSNP","start":140497293,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140497293,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795465474"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1413746231","source":"dbSNP","start":140497298,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140497298,"feature_type":"variation","strand":1},{"id":"rs1373567225","seq_region_name":"7","clinical_significance":[],"start":140497299,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140497299,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497305,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140497305,"seq_region_name":"7","id":"rs2130415628","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497307,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140497307,"id":"rs1585519811","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140497308,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140497308,"alleles":["T","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1772334746"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497313,"source":"dbSNP","strand":1,"feature_type":"variation","end":140497313,"alleles":["A","G"],"seq_region_name":"7","id":"rs778626907","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795465579","source":"dbSNP","start":140497315,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140497315,"feature_type":"variation","strand":1},{"end":140497316,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140497316,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs887436409","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795465631","clinical_significance":[],"start":140497317,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140497317,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"alleles":["A","G"],"end":140497318,"feature_type":"variation","strand":1,"source":"dbSNP","start":140497318,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795465650"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795465673","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497325,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140497325},{"source":"dbSNP","start":140497330,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C","G"],"end":140497330,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1324707217","seq_region_name":"7"},{"id":"rs1795465727","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497331,"source":"dbSNP","strand":1,"feature_type":"variation","end":140497331,"alleles":["G","A"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497333,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140497333,"seq_region_name":"7","id":"rs745514183","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497335,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140497335,"seq_region_name":"7","id":"rs1795465770","clinical_significance":[]},{"id":"rs1795465792","seq_region_name":"7","clinical_significance":[],"start":140497338,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140497338,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1333204930","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497340,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140497340},{"clinical_significance":[],"seq_region_name":"7","id":"rs1165473203","end":140497341,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140497341,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140497342,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497342,"clinical_significance":[],"id":"rs574901054","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140497343,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497343,"source":"dbSNP","seq_region_name":"7","id":"rs1795465876","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140497344,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497344,"source":"dbSNP","seq_region_name":"7","id":"rs1463090769","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140497346,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497346,"clinical_significance":[],"seq_region_name":"7","id":"rs1415701236"},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140497347,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497347,"clinical_significance":[],"seq_region_name":"7","id":"rs1231522368"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140497352,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497352,"source":"dbSNP","id":"rs1563105866","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795465995","clinical_significance":[],"strand":1,"feature_type":"variation","end":140497357,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497357,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140497361,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497361,"clinical_significance":[],"id":"rs1795466008","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1187536194","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140497362,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497362,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497365,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140497365,"clinical_significance":[],"seq_region_name":"7","id":"rs1419953533"},{"seq_region_name":"7","id":"rs1282288370","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140497366,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497366,"source":"dbSNP"},{"source":"dbSNP","start":140497368,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140497368,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130415704"},{"seq_region_name":"7","id":"rs909328745","clinical_significance":[],"end":140497372,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140497372,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140497374,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140497376,"alleles":["GGG","GG"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795466088","clinical_significance":[]},{"start":140497381,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140497381,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1329396969","clinical_significance":[]},{"source":"dbSNP","start":140497389,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140497389,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795466122"},{"alleles":["C","T"],"end":140497392,"strand":1,"feature_type":"variation","start":140497392,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1252917268","clinical_significance":[]},{"seq_region_name":"7","id":"rs368530173","clinical_significance":[],"alleles":["G","A"],"end":140497395,"strand":1,"feature_type":"variation","start":140497395,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497397,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140497397,"clinical_significance":[],"seq_region_name":"7","id":"rs1795466186"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585519836","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497407,"feature_type":"variation","strand":1,"end":140497407,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1795466239","clinical_significance":[],"end":140497410,"alleles":["CCCC","CCCCC"],"strand":1,"feature_type":"variation","start":140497407,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497408,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140497408,"clinical_significance":[],"id":"rs573148932","seq_region_name":"7"},{"end":140497415,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140497415,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1480474474","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497416,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140497416,"clinical_significance":[],"seq_region_name":"7","id":"rs144083633"},{"id":"rs1585519849","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140497421,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497421,"source":"dbSNP"},{"clinical_significance":[],"id":"rs540190069","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140497423,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497423},{"source":"dbSNP","start":140497427,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140497427,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795466387"},{"seq_region_name":"7","id":"rs1795466412","clinical_significance":[],"start":140497432,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140497432,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"alleles":["G","A"],"end":140497433,"feature_type":"variation","strand":1,"source":"dbSNP","start":140497433,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs188051739"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140497434,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497434,"source":"dbSNP","seq_region_name":"7","id":"rs1485223341","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497436,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140497436,"seq_region_name":"7","id":"rs1795466506","clinical_significance":[]},{"end":140497438,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140497438,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795466542","clinical_significance":[]},{"source":"dbSNP","start":140497439,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140497439,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1336346625","seq_region_name":"7"},{"seq_region_name":"7","id":"rs2130415773","clinical_significance":[],"start":140497442,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140497442,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"end":140497444,"alleles":["A","G","T"],"strand":1,"feature_type":"variation","start":140497444,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1270771424","clinical_significance":[]},{"start":140497447,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140497447,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1210377646","clinical_significance":[]},{"end":140497448,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140497448,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs545345202"},{"clinical_significance":[],"seq_region_name":"7","id":"rs933602293","feature_type":"variation","strand":1,"alleles":["G","C","T"],"end":140497452,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497452},{"seq_region_name":"7","id":"rs1389465312","clinical_significance":[],"alleles":["T","C"],"end":140497453,"strand":1,"feature_type":"variation","start":140497453,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497456,"feature_type":"variation","strand":1,"end":140497456,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1036056293"},{"clinical_significance":[],"id":"rs1326520322","seq_region_name":"7","source":"dbSNP","start":140497458,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140497458,"alleles":["G","A"],"feature_type":"variation","strand":1},{"alleles":["T","A"],"end":140497467,"strand":1,"feature_type":"variation","start":140497467,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1442955572","clinical_significance":[]},{"seq_region_name":"7","id":"rs1051095629","clinical_significance":[],"start":140497469,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140497469,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs371834231","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497476,"feature_type":"variation","strand":1,"end":140497476,"alleles":["C","T"]},{"strand":1,"feature_type":"variation","end":140497479,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497479,"source":"dbSNP","seq_region_name":"7","id":"rs1392157273","clinical_significance":[]},{"start":140497482,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140497482,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs1795467259","seq_region_name":"7","clinical_significance":[]},{"id":"rs557451161","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497483,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140497483},{"seq_region_name":"7","id":"rs1795467320","clinical_significance":[],"start":140497494,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140497494,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1795467350","seq_region_name":"7","source":"dbSNP","start":140497498,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140497498,"alleles":["G","C"],"feature_type":"variation","strand":1},{"id":"rs1454374123","seq_region_name":"7","clinical_significance":[],"start":140497499,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140497499,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497500,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140497500,"clinical_significance":[],"seq_region_name":"7","id":"rs1198378396"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795467445","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497507,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140497507},{"alleles":["A","G"],"end":140497509,"strand":1,"feature_type":"variation","start":140497509,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1011225731","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497519,"source":"dbSNP","strand":1,"feature_type":"variation","end":140497519,"alleles":["T","C"],"seq_region_name":"7","id":"rs1268506108","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497521,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140497521,"id":"rs1795467534","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1473053226","alleles":["C","G","T"],"end":140497522,"feature_type":"variation","strand":1,"source":"dbSNP","start":140497522,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497534,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140497534,"clinical_significance":[],"seq_region_name":"7","id":"rs1795467597"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497536,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140497536,"clinical_significance":[],"seq_region_name":"7","id":"rs1467563476"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795467648","source":"dbSNP","start":140497540,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140497540,"feature_type":"variation","strand":1},{"id":"rs113628000","seq_region_name":"7","clinical_significance":[],"end":140497542,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140497542,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1028750305","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497543,"source":"dbSNP","strand":1,"feature_type":"variation","end":140497543,"alleles":["C","G","T"]},{"strand":1,"feature_type":"variation","end":140497551,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497551,"source":"dbSNP","seq_region_name":"7","id":"rs1485869487","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs775166048","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140497555,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497555},{"clinical_significance":[],"seq_region_name":"7","id":"rs1236369073","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497560,"feature_type":"variation","strand":1,"end":140497560,"alleles":["G","A"]},{"end":140497561,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140497561,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs953299061","clinical_significance":[]},{"start":140497564,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140497564,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795467864","clinical_significance":[]},{"source":"dbSNP","start":140497567,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140497567,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs550751921"},{"end":140497575,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140497575,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1303926580","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1236209580","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497579,"feature_type":"variation","strand":1,"end":140497580,"alleles":["CC","C"]},{"source":"dbSNP","start":140497582,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140497582,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795467966"},{"start":140497586,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AA","A"],"end":140497587,"strand":1,"feature_type":"variation","id":"rs766718332","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1164409521","clinical_significance":[],"end":140497593,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140497593,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1382863652","end":140497596,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140497596,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1585519911","seq_region_name":"7","feature_type":"variation","strand":1,"end":140497598,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497598},{"end":140497601,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140497601,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2363815","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140497603,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497603,"clinical_significance":[],"seq_region_name":"7","id":"rs1287368346"},{"alleles":["C","T"],"end":140497609,"feature_type":"variation","strand":1,"source":"dbSNP","start":140497609,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795468236"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497610,"feature_type":"variation","strand":1,"end":140497610,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130415925"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1297154561","alleles":["C","A"],"end":140497614,"feature_type":"variation","strand":1,"source":"dbSNP","start":140497614,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497615,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140497615,"clinical_significance":[],"id":"rs1395897411","seq_region_name":"7"},{"seq_region_name":"7","id":"rs998526130","clinical_significance":[],"start":140497617,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140497617,"alleles":["A","G","T"],"strand":1,"feature_type":"variation"},{"end":140497618,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140497618,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795468351"},{"start":140497619,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140497619,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795468375","clinical_significance":[]},{"start":140497621,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140497621,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585519927","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140497624,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497624,"clinical_significance":[],"seq_region_name":"7","id":"rs1452957651"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795468470","alleles":["C","T"],"end":140497626,"feature_type":"variation","strand":1,"source":"dbSNP","start":140497626,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1035540708","feature_type":"variation","strand":1,"end":140497631,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497631},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497633,"source":"dbSNP","strand":1,"feature_type":"variation","end":140497633,"alleles":["C","G"],"id":"rs1795468502","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs530147489","alleles":["C","G"],"end":140497637,"feature_type":"variation","strand":1,"source":"dbSNP","start":140497637,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795468561","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497645,"feature_type":"variation","strand":1,"end":140497645,"alleles":["A","T"]},{"feature_type":"variation","strand":1,"end":140497649,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497649,"clinical_significance":[],"id":"rs1194445171","seq_region_name":"7"},{"start":140497650,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140497650,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs895614865","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140497656,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497656,"clinical_significance":[],"seq_region_name":"7","id":"rs1795468613"},{"source":"dbSNP","start":140497659,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140497659,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1428615415","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1012734360","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140497660,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497660},{"clinical_significance":[],"seq_region_name":"7","id":"rs1263168986","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497662,"feature_type":"variation","strand":1,"end":140497662,"alleles":["G","T"]},{"start":140497669,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140497669,"strand":1,"feature_type":"variation","id":"rs1563105917","seq_region_name":"7","clinical_significance":[]},{"id":"rs1795468701","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","-"],"end":140497669,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497669,"source":"dbSNP"},{"seq_region_name":"7","id":"rs558355243","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["TTTT","TTTTT"],"end":140497677,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497674,"source":"dbSNP"},{"seq_region_name":"7","id":"rs988268764","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140497676,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497676,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497677,"feature_type":"variation","strand":1,"end":140497677,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585519946"},{"source":"dbSNP","start":140497683,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140497683,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1023330300"},{"source":"dbSNP","start":140497687,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140497687,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130416000"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130416004","alleles":["G","T"],"end":140497692,"feature_type":"variation","strand":1,"source":"dbSNP","start":140497692,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1212764872","source":"dbSNP","start":140497700,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140497700,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795468920","clinical_significance":[],"start":140497704,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140497704,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140497706,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497706,"source":"dbSNP","seq_region_name":"7","id":"rs2130416013","clinical_significance":[]},{"seq_region_name":"7","id":"rs548148512","clinical_significance":[],"alleles":["A","G"],"end":140497707,"strand":1,"feature_type":"variation","start":140497707,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140497708,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140497708,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs193031835"},{"start":140497712,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140497712,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1228015049","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795469008","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497715,"feature_type":"variation","strand":1,"end":140497715,"alleles":["C","T"]},{"source":"dbSNP","start":140497718,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140497718,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs984826682"},{"start":140497719,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140497719,"alleles":["A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795469056","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795469078","clinical_significance":[],"start":140497734,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140497736,"alleles":["TAT","T"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140497735,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140497735,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585519961"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1243554860","end":140497739,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140497739,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1016232879","source":"dbSNP","start":140497741,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140497741,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs962130482","seq_region_name":"7","alleles":["A","T"],"end":140497743,"feature_type":"variation","strand":1,"source":"dbSNP","start":140497743,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140497751,"alleles":["TTTTTTTT","TTTTTTT","TTTTTTTTT"],"strand":1,"feature_type":"variation","start":140497744,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1286013797","clinical_significance":[]},{"alleles":["T","A","G"],"end":140497747,"strand":1,"feature_type":"variation","start":140497747,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs972116141","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140497752,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140497752,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795469347","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795469374","clinical_significance":[],"start":140497756,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140497756,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"id":"rs1795469400","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140497757,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497757,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140497758,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497758,"source":"dbSNP","id":"rs1585519974","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795469468","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497759,"source":"dbSNP","strand":1,"feature_type":"variation","end":140497759,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs182901897","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497760,"source":"dbSNP","strand":1,"feature_type":"variation","end":140497760,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs367699073","clinical_significance":[],"strand":1,"feature_type":"variation","end":140497762,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497762,"source":"dbSNP"},{"seq_region_name":"7","id":"rs2885917","clinical_significance":[],"start":140497763,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140497763,"alleles":["G","A","C","T"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140497764,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140497764,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs986302869","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497765,"feature_type":"variation","strand":1,"end":140497765,"alleles":["G","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs910830190"},{"source":"dbSNP","start":140497766,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140497766,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1354135976"},{"id":"rs1795469755","seq_region_name":"7","clinical_significance":[],"start":140497770,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140497770,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs2130416099","clinical_significance":[],"start":140497771,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140497771,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs947637944","source":"dbSNP","start":140497772,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140497772,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs2130416108","clinical_significance":[],"start":140497773,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140497772,"alleles":["-","TGG"],"strand":1,"feature_type":"variation"},{"alleles":["C","T"],"end":140497774,"feature_type":"variation","strand":1,"source":"dbSNP","start":140497774,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs762229755"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1275123789","end":140497775,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140497775,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140497781,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140497781,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130416129","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795469885","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140497787,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497787},{"seq_region_name":"7","id":"rs1483874774","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140497793,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497793,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497799,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140497799,"seq_region_name":"7","id":"rs1795469948","clinical_significance":[]},{"seq_region_name":"7","id":"rs1184628603","clinical_significance":[],"strand":1,"feature_type":"variation","end":140497805,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497805,"source":"dbSNP"},{"seq_region_name":"7","id":"rs2130416151","clinical_significance":[],"strand":1,"feature_type":"variation","end":140497815,"alleles":["ACTGCAAC","AC"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497808,"source":"dbSNP"},{"end":140497810,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140497810,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1477172811","clinical_significance":[]},{"alleles":["C","T"],"end":140497815,"strand":1,"feature_type":"variation","start":140497815,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795470044","seq_region_name":"7","clinical_significance":[]},{"id":"rs1795470073","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140497818,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497818,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1248671013","end":140497819,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140497819,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795470126","alleles":["C","T"],"end":140497821,"feature_type":"variation","strand":1,"source":"dbSNP","start":140497821,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140497822,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497822,"clinical_significance":[],"seq_region_name":"7","id":"rs1418619923"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497826,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140497826,"clinical_significance":[],"seq_region_name":"7","id":"rs1795470177"},{"feature_type":"variation","strand":1,"end":140497827,"alleles":["G","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497827,"clinical_significance":[],"seq_region_name":"7","id":"rs765523432"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497828,"source":"dbSNP","strand":1,"feature_type":"variation","end":140497828,"alleles":["G","T"],"seq_region_name":"7","id":"rs1795470329","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795470358","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140497829,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497829},{"clinical_significance":[],"seq_region_name":"7","id":"rs1277703208","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497832,"feature_type":"variation","strand":1,"end":140497832,"alleles":["C","G"]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140497836,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497836,"source":"dbSNP","seq_region_name":"7","id":"rs1795470421","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795470451","clinical_significance":[],"start":140497837,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140497837,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140497840,"alleles":["TT","TTT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497839,"clinical_significance":[],"seq_region_name":"7","id":"rs1795470483"},{"seq_region_name":"7","id":"rs934428813","clinical_significance":[],"start":140497843,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140497843,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497846,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140497846,"seq_region_name":"7","id":"rs1795470554","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497847,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140497847,"seq_region_name":"7","id":"rs1795470583","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140497855,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497855,"clinical_significance":[],"id":"rs1795470608","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497858,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140497858,"clinical_significance":[],"seq_region_name":"7","id":"rs1196138982"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497859,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140497859,"seq_region_name":"7","id":"rs1795470660","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140497865,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497865,"source":"dbSNP","seq_region_name":"7","id":"rs1341459617","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497867,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140497867,"seq_region_name":"7","id":"rs1057307212","clinical_significance":[]},{"alleles":["G","T"],"end":140497869,"strand":1,"feature_type":"variation","start":140497869,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1218094716","clinical_significance":[]},{"seq_region_name":"7","id":"rs1356104874","clinical_significance":[],"start":140497872,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140497872,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1295371728","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140497874,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497874,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs895553738","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497880,"feature_type":"variation","strand":1,"end":140497880,"alleles":["C","T"]},{"alleles":["A","G"],"end":140497881,"strand":1,"feature_type":"variation","start":140497881,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1340060487","clinical_significance":[]},{"end":140497882,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140497882,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs552633405","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140497883,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497883,"source":"dbSNP","seq_region_name":"7","id":"rs1423331735","clinical_significance":[]},{"clinical_significance":[],"id":"rs933032979","seq_region_name":"7","end":140497886,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140497886,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497887,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140497887,"clinical_significance":[],"id":"rs1163242120","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497892,"source":"dbSNP","strand":1,"feature_type":"variation","end":140497892,"alleles":["C","T"],"id":"rs1371575303","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1432006442","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497897,"source":"dbSNP","strand":1,"feature_type":"variation","end":140497897,"alleles":["C","G","T"]},{"id":"rs1795471680","seq_region_name":"7","clinical_significance":[],"end":140497898,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140497898,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["A","G"],"end":140497899,"feature_type":"variation","strand":1,"source":"dbSNP","start":140497899,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1464673546"},{"alleles":["A","G"],"end":140497900,"strand":1,"feature_type":"variation","start":140497900,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1050261282","clinical_significance":[]},{"seq_region_name":"7","id":"rs1745092603","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140497902,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497902,"source":"dbSNP"},{"seq_region_name":"7","id":"rs535263876","clinical_significance":[],"end":140497906,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140497906,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140497909,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497909,"clinical_significance":[],"seq_region_name":"7","id":"rs1022792543"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795471830","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140497916,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497916},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795471859","alleles":["AGACA","A"],"end":140497922,"feature_type":"variation","strand":1,"source":"dbSNP","start":140497918,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1372114726","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497924,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140497924},{"alleles":["G","C"],"end":140497926,"strand":1,"feature_type":"variation","start":140497926,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs888365979","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497927,"source":"dbSNP","strand":1,"feature_type":"variation","end":140497927,"alleles":["G","A","C"],"id":"rs888940688","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497929,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140497929,"clinical_significance":[],"id":"rs1795471997","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140497934,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497934,"source":"dbSNP","id":"rs1182338085","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140497934,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140497962,"alleles":["CCATGTTGGCCAGGCTAGTCTTGAATTCC","CC"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1236524982"},{"clinical_significance":[],"id":"rs1795472072","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497936,"feature_type":"variation","strand":1,"end":140497936,"alleles":["A","G"]},{"feature_type":"variation","strand":1,"end":140497940,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497940,"clinical_significance":[],"id":"rs1795472100","seq_region_name":"7"},{"alleles":["G","A"],"end":140497942,"strand":1,"feature_type":"variation","start":140497942,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795472130","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795472172","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497946,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140497946},{"seq_region_name":"7","id":"rs1000819379","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140497947,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497947,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795472231","alleles":["C","T"],"end":140497948,"feature_type":"variation","strand":1,"source":"dbSNP","start":140497948,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140497952,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140497952,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1396152064","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140497953,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497953,"clinical_significance":[],"seq_region_name":"7","id":"rs773423696"},{"seq_region_name":"7","id":"rs571021771","clinical_significance":[],"start":140497963,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140497963,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585520087","end":140497970,"alleles":["A","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140497970,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1197877907","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497972,"feature_type":"variation","strand":1,"end":140497972,"alleles":["G","A","T"]},{"alleles":["GTGA","-"],"end":140497975,"feature_type":"variation","strand":1,"source":"dbSNP","start":140497972,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795472388"},{"feature_type":"variation","strand":1,"end":140497980,"alleles":["GATTCAC","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497974,"clinical_significance":[],"seq_region_name":"7","id":"rs1275165251"},{"clinical_significance":[],"id":"rs1795472437","seq_region_name":"7","source":"dbSNP","start":140497977,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140497977,"alleles":["T","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1338148571","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497978,"feature_type":"variation","strand":1,"end":140497978,"alleles":["C","A"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497978,"source":"dbSNP","strand":1,"feature_type":"variation","end":140497981,"alleles":["CACC","C"],"seq_region_name":"7","id":"rs1795472504","clinical_significance":[]},{"alleles":["A","C"],"end":140497979,"strand":1,"feature_type":"variation","start":140497979,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585520088","clinical_significance":[]},{"id":"rs1016288369","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140497980,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497980,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1355980168","clinical_significance":[],"alleles":["C","A"],"end":140497981,"strand":1,"feature_type":"variation","start":140497981,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140497982,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140497982,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795472617","clinical_significance":[]},{"start":140497983,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140497983,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs376746704","clinical_significance":[]},{"seq_region_name":"7","id":"rs1280295423","clinical_significance":[],"start":140497987,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G","T"],"end":140497987,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs538009674","alleles":["G","A","C"],"end":140497988,"feature_type":"variation","strand":1,"source":"dbSNP","start":140497988,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140497989,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140497989,"clinical_significance":[],"id":"rs1331301666","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140497990,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140497990,"source":"dbSNP","seq_region_name":"7","id":"rs1442335812","clinical_significance":[]},{"seq_region_name":"7","id":"rs1275195031","clinical_significance":[],"start":140497991,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["CTCCCAAG","CTCCCAAGCTCCCAAG"],"end":140497998,"strand":1,"feature_type":"variation"},{"start":140497992,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140497992,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1397297017","clinical_significance":[]},{"clinical_significance":[],"id":"rs972074358","seq_region_name":"7","alleles":["G","A","C"],"end":140497998,"feature_type":"variation","strand":1,"source":"dbSNP","start":140497998,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1327401329","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498001,"feature_type":"variation","strand":1,"end":140498001,"alleles":["G","T"]},{"seq_region_name":"7","id":"rs1795472921","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140498004,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498004,"source":"dbSNP"},{"start":140498005,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140498005,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1024947652","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498007,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140498007,"clinical_significance":[],"seq_region_name":"7","id":"rs1585520111"},{"alleles":["G","A","T"],"end":140498013,"strand":1,"feature_type":"variation","start":140498013,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1158727661","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585520120","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498014,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140498014},{"start":140498015,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140498015,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs1795473074","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130416378","clinical_significance":[],"end":140498016,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140498016,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498021,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140498021,"clinical_significance":[],"id":"rs1030861470","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498025,"feature_type":"variation","strand":1,"end":140498025,"alleles":["C","A","T"],"clinical_significance":[],"id":"rs954810467","seq_region_name":"7"},{"start":140498026,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140498026,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs986744774","clinical_significance":[]},{"source":"dbSNP","start":140498027,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140498027,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1468895777"},{"start":140498028,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140498028,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1254798857","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140498031,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498031,"clinical_significance":[],"seq_region_name":"7","id":"rs556725931"},{"clinical_significance":[],"seq_region_name":"7","id":"rs910682580","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498032,"feature_type":"variation","strand":1,"end":140498032,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs368373639","feature_type":"variation","strand":1,"end":140498034,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498034},{"start":140498046,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140498046,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795473340","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140498047,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498047,"source":"dbSNP","seq_region_name":"7","id":"rs1795473362","clinical_significance":[]},{"clinical_significance":[],"id":"rs1585520145","seq_region_name":"7","alleles":["A","C","G"],"end":140498048,"feature_type":"variation","strand":1,"source":"dbSNP","start":140498048,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1033879664","seq_region_name":"7","feature_type":"variation","strand":1,"end":140498061,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498061},{"end":140498064,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140498064,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1201211771","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs952977591","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498067,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140498067},{"seq_region_name":"7","id":"rs984412039","clinical_significance":[],"strand":1,"feature_type":"variation","end":140498068,"alleles":["A","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498068,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498068,"source":"dbSNP","strand":1,"feature_type":"variation","end":140498075,"alleles":["AGTTAGTT","AGTT"],"id":"rs1795473531","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498073,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140498073,"seq_region_name":"7","id":"rs947652454","clinical_significance":[]},{"end":140498074,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140498074,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs978959422","clinical_significance":[]},{"start":140498077,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140498077,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795473613","clinical_significance":[]},{"alleles":["T","G"],"end":140498081,"feature_type":"variation","strand":1,"source":"dbSNP","start":140498081,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs940257194"},{"clinical_significance":[],"id":"rs1183580322","seq_region_name":"7","source":"dbSNP","start":140498083,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140498083,"alleles":["C","T"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140498088,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498088,"clinical_significance":[],"seq_region_name":"7","id":"rs1391326512"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1318599588","end":140498093,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140498093,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["G","-"],"end":140498094,"feature_type":"variation","strand":1,"source":"dbSNP","start":140498094,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1402121819"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795473751","source":"dbSNP","start":140498094,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140498094,"alleles":["G","A"],"feature_type":"variation","strand":1},{"id":"rs924846938","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498097,"source":"dbSNP","strand":1,"feature_type":"variation","end":140498097,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs2130416461","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498098,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140498098},{"seq_region_name":"7","id":"rs1451758038","clinical_significance":[],"start":140498101,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140498101,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs763106032","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140498103,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498103},{"clinical_significance":[],"id":"rs934356768","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140498105,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498105},{"seq_region_name":"7","id":"rs1358204575","clinical_significance":[],"alleles":["C","T"],"end":140498106,"strand":1,"feature_type":"variation","start":140498106,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795473925","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498109,"source":"dbSNP","strand":1,"feature_type":"variation","end":140498109,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs2130416479","clinical_significance":[],"end":140498112,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140498112,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140498115,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498115,"clinical_significance":[],"seq_region_name":"7","id":"rs1157884794"},{"seq_region_name":"7","id":"rs867317579","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140498119,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498119,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795474006","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140498124,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498124,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140498130,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498130,"source":"dbSNP","seq_region_name":"7","id":"rs1795474024","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498132,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140498132,"clinical_significance":[],"seq_region_name":"7","id":"rs1056789729"},{"start":140498133,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140498133,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs895591914","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498141,"source":"dbSNP","strand":1,"feature_type":"variation","end":140498141,"alleles":["T","A","C"],"seq_region_name":"7","id":"rs948456304","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140498148,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498148,"clinical_significance":[],"seq_region_name":"7","id":"rs1585520180"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563106021","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498150,"feature_type":"variation","strand":1,"alleles":["TCTCT","TCT"],"end":140498154},{"id":"rs1795474191","seq_region_name":"7","clinical_significance":[],"start":140498153,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140498153,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1477760229","clinical_significance":[],"alleles":["T","C"],"end":140498155,"strand":1,"feature_type":"variation","start":140498155,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1242821008","source":"dbSNP","start":140498166,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140498166,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1795474236","seq_region_name":"7","end":140498171,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140498171,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140498174,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140498174,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1218013094","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140498177,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498177,"clinical_significance":[],"seq_region_name":"7","id":"rs561760896"},{"seq_region_name":"7","id":"rs187749257","clinical_significance":[],"alleles":["G","A"],"end":140498178,"strand":1,"feature_type":"variation","start":140498178,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs888979636","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140498184,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498184,"source":"dbSNP"},{"seq_region_name":"7","id":"rs536376876","clinical_significance":[],"strand":1,"feature_type":"variation","end":140498187,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498187,"source":"dbSNP"},{"alleles":["C","G"],"end":140498200,"strand":1,"feature_type":"variation","start":140498200,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs143208026","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795474396","feature_type":"variation","strand":1,"end":140498201,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498201},{"clinical_significance":[],"id":"rs1795474410","seq_region_name":"7","feature_type":"variation","strand":1,"end":140498203,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498203},{"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140498207,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498207,"clinical_significance":[],"seq_region_name":"7","id":"rs192666214"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140498210,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498210,"clinical_significance":[],"seq_region_name":"7","id":"rs1795474460"},{"alleles":["G","A"],"end":140498211,"feature_type":"variation","strand":1,"source":"dbSNP","start":140498211,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795474482","seq_region_name":"7"},{"start":140498212,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140498212,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs892387688","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795474519","source":"dbSNP","start":140498214,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140498214,"alleles":["G","A"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498218,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140498218,"seq_region_name":"7","id":"rs1795474535","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140498221,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498221,"source":"dbSNP","id":"rs1795474552","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1363234112","feature_type":"variation","strand":1,"end":140498227,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498227},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795474587","source":"dbSNP","start":140498229,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140498229,"alleles":["C","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1270313893","clinical_significance":[],"end":140498230,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140498230,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["G","A"],"end":140498234,"feature_type":"variation","strand":1,"source":"dbSNP","start":140498234,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs755099245"},{"seq_region_name":"7","id":"rs1795474644","clinical_significance":[],"end":140498234,"alleles":["G","GG"],"strand":1,"feature_type":"variation","start":140498234,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140498241,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498241,"source":"dbSNP","id":"rs764007838","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs993939699","end":140498242,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140498242,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs753787163","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498243,"source":"dbSNP","strand":1,"feature_type":"variation","end":140498243,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130416572","source":"dbSNP","start":140498244,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140498244,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795474757","source":"dbSNP","start":140498245,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140498245,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1377011610","feature_type":"variation","strand":1,"end":140498246,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498246},{"id":"rs1413891467","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["TTT","TT"],"end":140498249,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498247,"source":"dbSNP"},{"seq_region_name":"7","id":"rs954962454","clinical_significance":[],"start":140498251,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140498251,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs2130416589","clinical_significance":[],"strand":1,"feature_type":"variation","end":140498252,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498252,"source":"dbSNP"},{"end":140498254,"alleles":["T","TT"],"strand":1,"feature_type":"variation","start":140498254,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795474950","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795474966","seq_region_name":"7","end":140498256,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140498256,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1007609295","seq_region_name":"7","clinical_significance":[],"start":140498260,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140498260,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1017746451","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140498263,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498263},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498265,"source":"dbSNP","strand":1,"feature_type":"variation","end":140498265,"alleles":["G","A"],"id":"rs968881319","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140498268,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498268,"clinical_significance":[],"id":"rs1585520229","seq_region_name":"7"},{"source":"dbSNP","start":140498269,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140498269,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795475067"},{"alleles":["T","C"],"end":140498270,"feature_type":"variation","strand":1,"source":"dbSNP","start":140498270,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs866778767","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140498271,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498271,"source":"dbSNP","seq_region_name":"7","id":"rs1795475109","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585520235","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140498273,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498273},{"id":"rs978886319","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140498274,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498274,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795475159","feature_type":"variation","strand":1,"end":140498277,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498277},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140498278,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498278,"clinical_significance":[],"seq_region_name":"7","id":"rs1486875537"},{"feature_type":"variation","strand":1,"end":140498290,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498290,"clinical_significance":[],"id":"rs1795475197","seq_region_name":"7"},{"source":"dbSNP","start":140498291,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140498291,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795475211"},{"seq_region_name":"7","id":"rs1278689220","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498293,"source":"dbSNP","strand":1,"feature_type":"variation","end":140498301,"alleles":["CAGACCCAG","CAG"]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140498299,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498299,"clinical_significance":[],"seq_region_name":"7","id":"rs1209823008"},{"alleles":["G","A"],"end":140498305,"feature_type":"variation","strand":1,"source":"dbSNP","start":140498305,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795475262"},{"source":"dbSNP","start":140498306,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140498306,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs924900625","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498310,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140498310,"seq_region_name":"7","id":"rs1257974945","clinical_significance":[]},{"id":"rs1795475314","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140498312,"strand":1,"feature_type":"variation","start":140498312,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140498315,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498315,"clinical_significance":[],"seq_region_name":"7","id":"rs73735363"},{"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140498320,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498320,"clinical_significance":[],"id":"rs1034160427","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498323,"source":"dbSNP","strand":1,"feature_type":"variation","end":140498323,"alleles":["C","G","T"],"seq_region_name":"7","id":"rs992904727","clinical_significance":[]},{"id":"rs916887459","seq_region_name":"7","clinical_significance":[],"start":140498324,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140498324,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498330,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140498330,"seq_region_name":"7","id":"rs778589566","clinical_significance":[]},{"start":140498333,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140498337,"alleles":["GAGAG","GAG"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795475461","clinical_significance":[]},{"source":"dbSNP","start":140498334,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140498334,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs948488022","seq_region_name":"7"},{"id":"rs558522908","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140498335,"strand":1,"feature_type":"variation","start":140498335,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140498338,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140498338,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1415065916"},{"end":140498342,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140498342,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs909616745","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498345,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140498345,"id":"rs941205234","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1356955571","seq_region_name":"7","source":"dbSNP","start":140498346,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140498346,"alleles":["G","A","T"],"feature_type":"variation","strand":1},{"end":140498347,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140498347,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1466653964"},{"id":"rs1795475599","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498348,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140498348},{"alleles":["G","C"],"end":140498349,"feature_type":"variation","strand":1,"source":"dbSNP","start":140498349,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795475623"},{"id":"rs1795475646","seq_region_name":"7","clinical_significance":[],"end":140498351,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140498351,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1447011527","alleles":["G","A","C"],"end":140498353,"feature_type":"variation","strand":1,"source":"dbSNP","start":140498353,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585520281","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498355,"feature_type":"variation","strand":1,"end":140498355,"alleles":["T","G"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498356,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140498356,"seq_region_name":"7","id":"rs1185245501","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498356,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AGA","AGACAGA"],"end":140498358,"seq_region_name":"7","id":"rs1355043479","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs7781853","source":"dbSNP","start":140498359,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140498359,"alleles":["G","C","T"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498360,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140498360,"clinical_significance":[],"seq_region_name":"7","id":"rs897114275"},{"feature_type":"variation","strand":1,"end":140498361,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498361,"clinical_significance":[],"seq_region_name":"7","id":"rs1165708998"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795475886","feature_type":"variation","strand":1,"end":140498363,"alleles":["G","GG"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498363},{"end":140498370,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140498370,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795475911","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs998074853","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140498371,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498371,"source":"dbSNP"},{"id":"rs1563106077","seq_region_name":"7","clinical_significance":[],"start":140498372,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","G"],"end":140498372,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140498373,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498373,"clinical_significance":[],"seq_region_name":"7","id":"rs2130416765"},{"id":"rs1795475967","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498377,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140498377},{"start":140498381,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140498381,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1254315496","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498382,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140498382,"id":"rs1795476004","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498386,"feature_type":"variation","strand":1,"alleles":["GG","G"],"end":140498387,"clinical_significance":[],"seq_region_name":"7","id":"rs1795476022"},{"seq_region_name":"7","id":"rs1795476049","clinical_significance":[],"start":140498389,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140498389,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"start":140498390,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140498390,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1052208804","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498392,"feature_type":"variation","strand":1,"end":140498392,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795476078"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140498396,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498396,"source":"dbSNP","seq_region_name":"7","id":"rs1795476096","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498398,"feature_type":"variation","strand":1,"end":140498398,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1481123889"},{"clinical_significance":[],"id":"rs890437919","seq_region_name":"7","end":140498402,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140498402,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["ATA","A"],"end":140498404,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498402,"source":"dbSNP","seq_region_name":"7","id":"rs1795476151","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795476167","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498404,"feature_type":"variation","strand":1,"end":140498404,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs1795476183","clinical_significance":[],"alleles":["G","C"],"end":140498405,"strand":1,"feature_type":"variation","start":140498405,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498406,"source":"dbSNP","strand":1,"feature_type":"variation","end":140498406,"alleles":["T","C"],"id":"rs1795476203","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585520323","clinical_significance":[],"end":140498413,"alleles":["T","C","G"],"strand":1,"feature_type":"variation","start":140498413,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs779898448","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498430,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140498430},{"source":"dbSNP","start":140498431,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140498431,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1007953294"},{"alleles":["T","C"],"end":140498435,"feature_type":"variation","strand":1,"source":"dbSNP","start":140498435,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs544040798"},{"end":140498442,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140498442,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1317815757","seq_region_name":"7"},{"id":"rs1563106081","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498443,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140498443},{"seq_region_name":"7","id":"rs2885916","clinical_significance":[],"alleles":["C","A","G","T"],"end":140498446,"strand":1,"feature_type":"variation","start":140498446,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1795476499","seq_region_name":"7","clinical_significance":[],"start":140498453,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140498453,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140498455,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498455,"source":"dbSNP","seq_region_name":"7","id":"rs1795476515","clinical_significance":[]},{"id":"rs1468880091","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140498456,"strand":1,"feature_type":"variation","start":140498456,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795476554","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498459,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140498459},{"seq_region_name":"7","id":"rs151246605","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498461,"source":"dbSNP","strand":1,"feature_type":"variation","end":140498461,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1336580385","source":"dbSNP","start":140498462,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140498462,"alleles":["T","A"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498463,"feature_type":"variation","strand":1,"end":140498463,"alleles":["C","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795476642"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498464,"feature_type":"variation","strand":1,"end":140498464,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795476657"},{"end":140498466,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140498466,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs985738351","clinical_significance":[]},{"source":"dbSNP","start":140498468,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140498468,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs140458769"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795476750","alleles":["GGG","GG"],"end":140498473,"feature_type":"variation","strand":1,"source":"dbSNP","start":140498471,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1373729770","source":"dbSNP","start":140498473,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140498473,"alleles":["G","C"],"feature_type":"variation","strand":1},{"end":140498478,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140498478,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1299846199"},{"feature_type":"variation","strand":1,"end":140498487,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498487,"clinical_significance":[],"seq_region_name":"7","id":"rs936402708"},{"seq_region_name":"7","id":"rs1795476803","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498490,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140498490},{"alleles":["T","G"],"end":140498491,"feature_type":"variation","strand":1,"source":"dbSNP","start":140498491,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795476821"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1399430513","feature_type":"variation","strand":1,"end":140498492,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498492},{"id":"rs1326727535","seq_region_name":"7","clinical_significance":[],"start":140498497,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140498497,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs763334614","source":"dbSNP","start":140498498,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C","T"],"end":140498498,"feature_type":"variation","strand":1},{"alleles":["G","T"],"end":140498499,"feature_type":"variation","strand":1,"source":"dbSNP","start":140498499,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs764388715"},{"id":"rs1795476983","seq_region_name":"7","clinical_significance":[],"start":140498500,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140498500,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498501,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140498501,"id":"rs183559293","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140498502,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498502,"clinical_significance":[],"seq_region_name":"7","id":"rs1164273067"},{"alleles":["A","C"],"end":140498514,"strand":1,"feature_type":"variation","start":140498514,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1420086911","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs913730565","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140498518,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498518},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498519,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140498519,"clinical_significance":[],"id":"rs1795477073","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140498525,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498525,"source":"dbSNP","seq_region_name":"7","id":"rs2130416917","clinical_significance":[]},{"alleles":["T","G"],"end":140498526,"strand":1,"feature_type":"variation","start":140498526,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795477093","clinical_significance":[]},{"source":"dbSNP","start":140498528,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140498528,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs945307117"},{"id":"rs1795477133","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140498529,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498529,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1046332284","source":"dbSNP","start":140498533,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140498533,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140498538,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498538,"source":"dbSNP","id":"rs1795477170","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795477191","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498541,"source":"dbSNP","strand":1,"feature_type":"variation","end":140498541,"alleles":["C","T"]},{"strand":1,"feature_type":"variation","end":140498543,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498543,"source":"dbSNP","seq_region_name":"7","id":"rs1795477221","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140498546,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498546,"clinical_significance":[],"seq_region_name":"7","id":"rs1795477249"},{"clinical_significance":[],"id":"rs1031758752","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498549,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140498549},{"seq_region_name":"7","id":"rs1795477294","clinical_significance":[],"strand":1,"feature_type":"variation","end":140498555,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498555,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795477320","clinical_significance":[],"end":140498557,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140498557,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs748614654","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140498564,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498564},{"seq_region_name":"7","id":"rs1795477377","clinical_significance":[],"end":140498565,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140498565,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs114048143","clinical_significance":[],"start":140498566,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140498566,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1795477443","clinical_significance":[],"alleles":["T","A"],"end":140498568,"strand":1,"feature_type":"variation","start":140498568,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795477467","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498573,"source":"dbSNP","strand":1,"feature_type":"variation","end":140498573,"alleles":["G","A"]},{"end":140498577,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140498577,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130416977"},{"strand":1,"feature_type":"variation","alleles":["TGTTG","TGTTGTTG"],"end":140498583,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498579,"source":"dbSNP","seq_region_name":"7","id":"rs2130416980","clinical_significance":[]},{"id":"rs1220730495","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140498585,"strand":1,"feature_type":"variation","start":140498585,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140498590,"alleles":["AAAAA","AAAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140498586,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1002222576"},{"alleles":["A","G"],"end":140498590,"strand":1,"feature_type":"variation","start":140498590,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130416989","clinical_significance":[]},{"alleles":["G","A"],"end":140498593,"feature_type":"variation","strand":1,"source":"dbSNP","start":140498593,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1220320849"},{"end":140498594,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140498594,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795477587","clinical_significance":[]},{"end":140498595,"alleles":["C","CCGGC"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140498595,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585520418"},{"start":140498597,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140498597,"strand":1,"feature_type":"variation","id":"rs1317105557","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs114602075","seq_region_name":"7","source":"dbSNP","start":140498601,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140498601,"alleles":["C","T"],"feature_type":"variation","strand":1},{"alleles":["G","C"],"end":140498604,"feature_type":"variation","strand":1,"source":"dbSNP","start":140498604,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1321651064","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs969775762","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498607,"feature_type":"variation","strand":1,"end":140498607,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1795477767","clinical_significance":[],"strand":1,"feature_type":"variation","end":140498608,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498608,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795477790","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498615,"source":"dbSNP","strand":1,"feature_type":"variation","end":140498615,"alleles":["C","A"]},{"feature_type":"variation","strand":1,"end":140498618,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498618,"clinical_significance":[],"seq_region_name":"7","id":"rs1795477809"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563106117","feature_type":"variation","strand":1,"end":140498621,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498621},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498622,"feature_type":"variation","strand":1,"end":140498622,"alleles":["T","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795477856"},{"id":"rs571017211","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140498625,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498625,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140498626,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498626,"source":"dbSNP","seq_region_name":"7","id":"rs1223085066","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140498628,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498628,"clinical_significance":[],"seq_region_name":"7","id":"rs1585520429"},{"start":140498629,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140498629,"alleles":["T","C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795477953","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795477974","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498630,"source":"dbSNP","strand":1,"feature_type":"variation","end":140498630,"alleles":["G","A"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498634,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140498634,"clinical_significance":[],"seq_region_name":"7","id":"rs1795478001"},{"alleles":["A","G"],"end":140498640,"strand":1,"feature_type":"variation","start":140498640,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130417034","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs979753596","feature_type":"variation","strand":1,"end":140498641,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498641},{"clinical_significance":[],"seq_region_name":"7","id":"rs1443211244","end":140498644,"alleles":["TTT","TTTT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140498642,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["T","C"],"end":140498644,"strand":1,"feature_type":"variation","start":140498644,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795478092","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140498657,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498657,"source":"dbSNP","seq_region_name":"7","id":"rs1795478120","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795478139","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140498660,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498660},{"seq_region_name":"7","id":"rs1268886443","clinical_significance":[],"end":140498665,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140498665,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs551765742","clinical_significance":[],"end":140498666,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140498666,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs909669175","source":"dbSNP","start":140498669,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140498669,"alleles":["T","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563106127","end":140498670,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140498670,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1292986204","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498672,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140498672},{"seq_region_name":"7","id":"rs1795478288","clinical_significance":[],"end":140498673,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140498673,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140498675,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140498675,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1055103997","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs888536841","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140498687,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498687,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140498688,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498688,"source":"dbSNP","seq_region_name":"7","id":"rs1157304729","clinical_significance":[]},{"seq_region_name":"7","id":"rs1439400632","clinical_significance":[],"start":140498689,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140498689,"strand":1,"feature_type":"variation"},{"alleles":["C","T"],"end":140498690,"strand":1,"feature_type":"variation","start":140498690,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1396227164","clinical_significance":[]},{"id":"rs532049374","seq_region_name":"7","clinical_significance":[],"start":140498693,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","T"],"end":140498693,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498697,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140498697,"id":"rs150424557","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1264699627","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498698,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140498698},{"seq_region_name":"7","id":"rs918393304","clinical_significance":[],"end":140498699,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140498699,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795478529","source":"dbSNP","start":140498701,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140498701,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["AT","ATAGCAAGACCCTGTCTAT"],"end":140498704,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498703,"clinical_significance":[],"id":"rs2130417107","seq_region_name":"7"},{"id":"rs1193254765","seq_region_name":"7","clinical_significance":[],"start":140498704,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140498704,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"alleles":["T","TAGCAAGACCCTGTCTATTGATTTATTTATT","TAGCAAGACCCTGTCTATTGATTTATTTATTTGCTT","TAGCAAGACCCTGTCTATTGATTTATTTATTTGCTTT","TAGCAAGACCCTGTCTATTGATTTATTTATTTGCTTTT"],"end":140498704,"strand":1,"feature_type":"variation","start":140498704,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795478560","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498705,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["-","AGCAAGACCC","AGCAAGACCCTGTC"],"end":140498704,"id":"rs2130417120","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1267151388","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498705,"feature_type":"variation","strand":1,"end":140498705,"alleles":["T","A","C"]},{"source":"dbSNP","start":140498707,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140498707,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1479923653","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140498707,"alleles":["T","TCT","TCTATTGATTTATTTATTTGCTTTTT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498707,"clinical_significance":[],"seq_region_name":"7","id":"rs2130417129"},{"end":140498712,"alleles":["AAAAA","AAAAAA"],"strand":1,"feature_type":"variation","start":140498708,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1287707443","clinical_significance":[]},{"id":"rs1795478670","seq_region_name":"7","clinical_significance":[],"end":140498710,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140498710,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs2130417139","clinical_significance":[],"strand":1,"feature_type":"variation","end":140498711,"alleles":["-","CCCTGTCT","CCCTGTCTATTG","CCCTGTCTATTGATTT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498712,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs757634436","feature_type":"variation","strand":1,"alleles":["T","A"],"end":140498713,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498713},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130417144","feature_type":"variation","strand":1,"alleles":["TT","TTGATTTATTTATTTGCTTTTT"],"end":140498714,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498713},{"clinical_significance":[],"seq_region_name":"7","id":"rs1159355231","feature_type":"variation","strand":1,"alleles":["T","A"],"end":140498714,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498714},{"start":140498715,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["-","G"],"end":140498714,"strand":1,"feature_type":"variation","id":"rs2130417147","seq_region_name":"7","clinical_significance":[]},{"start":140498715,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140498715,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs138359144","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1016211192","end":140498722,"alleles":["AAAAAAAA","AAAAAAA","AAAAAAAAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140498715,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130417155","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498716,"feature_type":"variation","strand":1,"alleles":["-","TTTATTTATTTGCTTTTT"],"end":140498715},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140498720,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498720,"clinical_significance":[],"seq_region_name":"7","id":"rs189344827"},{"start":140498729,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["GGG","GG"],"end":140498731,"strand":1,"feature_type":"variation","id":"rs1795478838","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","C"],"end":140498732,"feature_type":"variation","strand":1,"source":"dbSNP","start":140498732,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs192378178"},{"seq_region_name":"7","id":"rs1329256748","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498737,"source":"dbSNP","strand":1,"feature_type":"variation","end":140498737,"alleles":["T","C"]},{"source":"dbSNP","start":140498742,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140498742,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1398436845","seq_region_name":"7"},{"end":140498743,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140498743,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs116650077","clinical_significance":[]},{"seq_region_name":"7","id":"rs1350362917","clinical_significance":[],"end":140498748,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140498748,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1795479009","seq_region_name":"7","clinical_significance":[],"start":140498750,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C","G"],"end":140498750,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs889686572","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498752,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140498752},{"strand":1,"feature_type":"variation","end":140498754,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498754,"source":"dbSNP","seq_region_name":"7","id":"rs1296519110","clinical_significance":[]},{"id":"rs1419506228","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140498755,"strand":1,"feature_type":"variation","start":140498755,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140498758,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498758,"clinical_significance":[],"id":"rs1301093025","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498762,"feature_type":"variation","strand":1,"end":140498762,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1376406210"},{"clinical_significance":[],"id":"rs943415434","seq_region_name":"7","source":"dbSNP","start":140498765,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140498765,"alleles":["C","A"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140498767,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498767,"clinical_significance":[],"id":"rs1175883464","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1465025165","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498773,"source":"dbSNP","strand":1,"feature_type":"variation","end":140498773,"alleles":["T","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130417199","alleles":["TT","TTT"],"end":140498781,"feature_type":"variation","strand":1,"source":"dbSNP","start":140498780,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["T","A"],"end":140498781,"strand":1,"feature_type":"variation","start":140498781,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1585520529","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs60287668","feature_type":"variation","strand":1,"alleles":["AAAAAAAAAAA","AAAAAAAAAA","AAAAAAAAAAAA","AAAAAAAAAAAAA"],"end":140498792,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498782},{"strand":1,"feature_type":"variation","alleles":["-","T"],"end":140498786,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498787,"source":"dbSNP","seq_region_name":"7","id":"rs1264898704","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1190992279","end":140498787,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140498787,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140498791,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140498791,"alleles":["A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1039006264","clinical_significance":[]},{"id":"rs1795479464","seq_region_name":"7","clinical_significance":[],"end":140498795,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140498795,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1487856383","clinical_significance":[],"strand":1,"feature_type":"variation","end":140498796,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498796,"source":"dbSNP"},{"end":140498800,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140498800,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs904618519"},{"source":"dbSNP","start":140498802,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140498802,"alleles":["T","A","C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs767125315"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1289160279","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498803,"feature_type":"variation","strand":1,"end":140498803,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs542239019","clinical_significance":[],"start":140498804,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140498804,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140498805,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","G","T"],"end":140498805,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1255271079"},{"id":"rs1031812646","seq_region_name":"7","clinical_significance":[],"start":140498806,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140498806,"alleles":["G","A","T"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140498808,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140498808,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs986211367"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1399674378","feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140498810,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498810},{"clinical_significance":[],"seq_region_name":"7","id":"rs891938615","end":140498811,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140498811,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498813,"source":"dbSNP","strand":1,"feature_type":"variation","end":140498813,"alleles":["C","T"],"id":"rs1795479747","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140498815,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498815,"clinical_significance":[],"seq_region_name":"7","id":"rs1284228003"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140498817,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498817,"clinical_significance":[],"seq_region_name":"7","id":"rs1322876085"},{"id":"rs1014820211","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140498818,"strand":1,"feature_type":"variation","start":140498818,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140498822,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140498822,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1402118940","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498823,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140498823,"clinical_significance":[],"id":"rs1563106179","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1168937943","clinical_significance":[],"alleles":["A","G"],"end":140498824,"strand":1,"feature_type":"variation","start":140498824,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140498829,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498829,"source":"dbSNP","id":"rs1795480013","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498830,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140498830,"clinical_significance":[],"seq_region_name":"7","id":"rs1563106184"},{"end":140498831,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140498831,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585520577","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1462070197","source":"dbSNP","start":140498832,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140498832,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795480140","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498835,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140498835},{"clinical_significance":[],"seq_region_name":"7","id":"rs184715608","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140498838,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498838},{"seq_region_name":"7","id":"rs749891795","clinical_significance":[],"strand":1,"feature_type":"variation","end":140498840,"alleles":["GGG","GG"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498838,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1477325642","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498841,"feature_type":"variation","strand":1,"end":140498841,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs189575589","alleles":["C","G","T"],"end":140498845,"feature_type":"variation","strand":1,"source":"dbSNP","start":140498845,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1585520593","clinical_significance":[],"start":140498846,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140498846,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"end":140498848,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140498848,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1257776432","clinical_significance":[]},{"end":140498852,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140498852,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs970708048","clinical_significance":[]},{"id":"rs1795480506","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498854,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140498854},{"clinical_significance":[],"seq_region_name":"7","id":"rs10237292","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498855,"feature_type":"variation","strand":1,"alleles":["G","A","C","T"],"end":140498855},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140498857,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498857,"clinical_significance":[],"seq_region_name":"7","id":"rs1255419381"},{"seq_region_name":"7","id":"rs1196268714","clinical_significance":[],"start":140498860,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140498860,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs767590546","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498861,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140498861},{"clinical_significance":[],"seq_region_name":"7","id":"rs1182521227","source":"dbSNP","start":140498862,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140498862,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1795480777","seq_region_name":"7","end":140498865,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140498865,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795480804","clinical_significance":[],"start":140498868,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140498872,"alleles":["AGGAG","AG"],"strand":1,"feature_type":"variation"},{"start":140498869,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140498869,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795480829","clinical_significance":[]},{"end":140498875,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140498875,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1253515228"},{"id":"rs1468188338","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498876,"source":"dbSNP","strand":1,"feature_type":"variation","end":140498876,"alleles":["A","G"]},{"strand":1,"feature_type":"variation","end":140498878,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498878,"source":"dbSNP","seq_region_name":"7","id":"rs1335809390","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795480950","clinical_significance":[],"strand":1,"feature_type":"variation","end":140498879,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498879,"source":"dbSNP"},{"start":140498880,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140498880,"alleles":["C","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795480974","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140498886,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498886,"source":"dbSNP","id":"rs1795480998","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498890,"feature_type":"variation","strand":1,"end":140498890,"alleles":["T","C"],"clinical_significance":[],"id":"rs989235186","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1176097623","alleles":["A","G"],"end":140498891,"feature_type":"variation","strand":1,"source":"dbSNP","start":140498891,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1413828286","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498892,"source":"dbSNP","strand":1,"feature_type":"variation","end":140498892,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795481111","source":"dbSNP","start":140498894,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140498894,"alleles":["A","G"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498895,"source":"dbSNP","strand":1,"feature_type":"variation","end":140498895,"alleles":["T","C"],"seq_region_name":"7","id":"rs181584724","clinical_significance":[]},{"alleles":["G","A"],"end":140498899,"strand":1,"feature_type":"variation","start":140498899,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1449701193","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140498900,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498900,"source":"dbSNP","id":"rs867950121","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs146660991","feature_type":"variation","strand":1,"end":140498903,"alleles":["A","C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498903},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498904,"feature_type":"variation","strand":1,"end":140498904,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1328773888"},{"clinical_significance":[],"seq_region_name":"7","id":"rs945172062","feature_type":"variation","strand":1,"end":140498906,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498906},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498907,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140498907,"seq_region_name":"7","id":"rs1795481300","clinical_significance":[]},{"seq_region_name":"7","id":"rs972449570","clinical_significance":[],"strand":1,"feature_type":"variation","end":140498909,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498909,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140498910,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498910,"clinical_significance":[],"seq_region_name":"7","id":"rs1795481359"},{"clinical_significance":[],"seq_region_name":"7","id":"rs184680342","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498911,"feature_type":"variation","strand":1,"end":140498911,"alleles":["C","G"]},{"alleles":["T","C"],"end":140498912,"feature_type":"variation","strand":1,"source":"dbSNP","start":140498912,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1471708161"},{"feature_type":"variation","strand":1,"end":140498913,"alleles":["A","C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498913,"clinical_significance":[],"seq_region_name":"7","id":"rs753755038"},{"id":"rs1441528962","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498914,"source":"dbSNP","strand":1,"feature_type":"variation","end":140498914,"alleles":["C","T"]},{"source":"dbSNP","start":140498916,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140498920,"alleles":["AAAAA","AAAA"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1236279686"},{"id":"rs1308938063","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498919,"source":"dbSNP","strand":1,"feature_type":"variation","end":140498919,"alleles":["A","G"]},{"start":140498924,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140498930,"alleles":["AAAAAAA","AAAAAA","AAAAAAAA"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1198090489","clinical_significance":[]},{"seq_region_name":"7","id":"rs1468920507","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498925,"source":"dbSNP","strand":1,"feature_type":"variation","end":140498925,"alleles":["A","G"]},{"alleles":["A","G"],"end":140498927,"strand":1,"feature_type":"variation","start":140498927,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795481615","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498928,"source":"dbSNP","strand":1,"feature_type":"variation","end":140498928,"alleles":["A","G"],"seq_region_name":"7","id":"rs555923794","clinical_significance":[]},{"source":"dbSNP","start":140498934,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140498934,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795481676"},{"seq_region_name":"7","id":"rs911177811","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498936,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140498936},{"seq_region_name":"7","id":"rs779019534","clinical_significance":[],"strand":1,"feature_type":"variation","end":140498952,"alleles":["CGGGCGTGGTGGCGGGC","CGGGC"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498936,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1355868217","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498937,"feature_type":"variation","strand":1,"end":140498937,"alleles":["G","A"]},{"id":"rs574330434","seq_region_name":"7","clinical_significance":[],"start":140498938,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140498938,"strand":1,"feature_type":"variation"},{"end":140498939,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140498939,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1279068347"},{"seq_region_name":"7","id":"rs1280567174","clinical_significance":[],"strand":1,"feature_type":"variation","end":140498940,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498940,"source":"dbSNP"},{"clinical_significance":[],"id":"rs541916625","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498941,"feature_type":"variation","strand":1,"end":140498941,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1039017978","clinical_significance":[],"alleles":["C","T"],"end":140498948,"strand":1,"feature_type":"variation","start":140498948,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1309097531","clinical_significance":[],"start":140498949,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140498949,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498951,"feature_type":"variation","strand":1,"end":140498951,"alleles":["G","A"],"clinical_significance":[],"id":"rs1795482009","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1445436209","clinical_significance":[],"strand":1,"feature_type":"variation","end":140498952,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498952,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140498953,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498953,"source":"dbSNP","seq_region_name":"7","id":"rs1795482065","clinical_significance":[]},{"seq_region_name":"7","id":"rs1554454053","clinical_significance":[],"start":140498954,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140498954,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs189396436","source":"dbSNP","start":140498957,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140498957,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140498971,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498971,"source":"dbSNP","id":"rs1795482153","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130417495","feature_type":"variation","strand":1,"end":140498973,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498973},{"clinical_significance":[],"seq_region_name":"7","id":"rs888446892","alleles":["A","G"],"end":140498977,"feature_type":"variation","strand":1,"source":"dbSNP","start":140498977,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498978,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140498978,"seq_region_name":"7","id":"rs1795482212","clinical_significance":[]},{"start":140498981,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140498981,"strand":1,"feature_type":"variation","id":"rs936104313","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795482265","feature_type":"variation","strand":1,"end":140498987,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498987},{"id":"rs1795482284","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498991,"source":"dbSNP","strand":1,"feature_type":"variation","end":140498991,"alleles":["G","C"]},{"seq_region_name":"7","id":"rs1585520660","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140498992,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498992,"source":"dbSNP"},{"start":140498994,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140498994,"alleles":["A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130417519","clinical_significance":[]},{"seq_region_name":"7","id":"rs139253563","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140498996,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140498996},{"clinical_significance":[],"seq_region_name":"7","id":"rs1389546784","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140498997,"feature_type":"variation","strand":1,"end":140498997,"alleles":["A","G"]},{"id":"rs1206270323","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499003,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140499003},{"clinical_significance":[],"seq_region_name":"7","id":"rs748102257","end":140499005,"alleles":["GCG","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140499003,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs891862646","source":"dbSNP","start":140499004,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140499004,"feature_type":"variation","strand":1},{"id":"rs534808547","seq_region_name":"7","clinical_significance":[],"start":140499004,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["CGTGAACCCCGGGAGGCAGAGTT","-"],"end":140499026,"strand":1,"feature_type":"variation"},{"end":140499005,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140499005,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1014459791","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1378417242","clinical_significance":[],"alleles":["TGAACCCCGGGAGGCAGAGTTTGTAGT","-"],"end":140499032,"strand":1,"feature_type":"variation","start":140499006,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["AACCCCGGGAGGCAGAGTTTGTAGT","-"],"end":140499032,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499008,"source":"dbSNP","id":"rs771888970","seq_region_name":"7","clinical_significance":[]},{"end":140499010,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140499010,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs369930433","seq_region_name":"7","clinical_significance":[]},{"end":140499013,"alleles":["CCCC","CCC"],"strand":1,"feature_type":"variation","start":140499010,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795482735","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499012,"source":"dbSNP","strand":1,"feature_type":"variation","end":140499012,"alleles":["C","A","T"],"seq_region_name":"7","id":"rs1454787666","clinical_significance":[]},{"start":140499013,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140499013,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs906119626","clinical_significance":[]},{"id":"rs897223085","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140499014,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499014,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1285140062","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499015,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140499015},{"source":"dbSNP","start":140499017,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140499017,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585520694"},{"id":"rs1795483215","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140499020,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499020,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140499024,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499024,"source":"dbSNP","seq_region_name":"7","id":"rs1001754891","clinical_significance":[]},{"source":"dbSNP","start":140499025,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TTTGT","TTTGTTTTGT"],"end":140499029,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795483259"},{"seq_region_name":"7","id":"rs1181742357","clinical_significance":[],"strand":1,"feature_type":"variation","end":140499027,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499027,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499028,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140499028,"seq_region_name":"7","id":"rs182017570","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499029,"feature_type":"variation","strand":1,"alleles":["TAGT","-"],"end":140499032,"clinical_significance":[],"seq_region_name":"7","id":"rs574748008"},{"start":140499031,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C"],"end":140499031,"strand":1,"feature_type":"variation","id":"rs1285973358","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795483458","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499033,"source":"dbSNP","strand":1,"feature_type":"variation","end":140499033,"alleles":["G","A"]},{"alleles":["G","C"],"end":140499040,"feature_type":"variation","strand":1,"source":"dbSNP","start":140499040,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795483474"},{"seq_region_name":"7","id":"rs1795483494","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499042,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140499042},{"seq_region_name":"7","id":"rs1449892215","clinical_significance":[],"start":140499043,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G","T"],"end":140499043,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1276169584","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140499044,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499044},{"id":"rs1433667560","seq_region_name":"7","clinical_significance":[],"start":140499045,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140499045,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499046,"source":"dbSNP","strand":1,"feature_type":"variation","end":140499046,"alleles":["A","C","G"],"id":"rs1330150084","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140499047,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140499047,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1298363563"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499049,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140499049,"seq_region_name":"7","id":"rs1795483605","clinical_significance":[]},{"source":"dbSNP","start":140499053,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140499053,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1421307607"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1011390774","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499054,"feature_type":"variation","strand":1,"end":140499054,"alleles":["A","C"]},{"end":140499056,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140499056,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1358347845","seq_region_name":"7","clinical_significance":[]},{"end":140499062,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140499062,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795483676","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1157795076","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140499066,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499066},{"id":"rs149428285","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140499070,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499070,"source":"dbSNP"},{"id":"rs954299549","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499075,"source":"dbSNP","strand":1,"feature_type":"variation","end":140499075,"alleles":["C","A"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499076,"feature_type":"variation","strand":1,"end":140499076,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1170900239"},{"seq_region_name":"7","id":"rs1585520725","clinical_significance":[],"end":140499079,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140499079,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1394017160","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499080,"feature_type":"variation","strand":1,"end":140499080,"alleles":["C","A","T"]},{"id":"rs1394947304","seq_region_name":"7","clinical_significance":[],"end":140499081,"alleles":["CC","CCC"],"strand":1,"feature_type":"variation","start":140499080,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795483837","feature_type":"variation","strand":1,"alleles":["CC","-"],"end":140499081,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499080},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795483859","feature_type":"variation","strand":1,"end":140499080,"alleles":["-","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499081},{"clinical_significance":[],"seq_region_name":"7","id":"rs1007143153","end":140499081,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140499081,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140499082,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C","G"],"end":140499082,"strand":1,"feature_type":"variation","id":"rs10254988","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs766233700","feature_type":"variation","strand":1,"end":140499082,"alleles":["A","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499082},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499084,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140499084,"id":"rs1795484012","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795484036","clinical_significance":[],"alleles":["-","CCTTT","CTTTT"],"end":140499084,"strand":1,"feature_type":"variation","start":140499085,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140499085,"alleles":["T","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499085,"source":"dbSNP","id":"rs868144480","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140499099,"alleles":["TTTTTTTTTTTTTTT","TTTTTTTT","TTTTTTTTTTT","TTTTTTTTTTTT","TTTTTTTTTTTTT","TTTTTTTTTTTTTT","TTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499085,"source":"dbSNP","seq_region_name":"7","id":"rs79163463","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140499086,"alleles":["T","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499086,"source":"dbSNP","id":"rs1359873902","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1297414837","source":"dbSNP","start":140499087,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140499087,"alleles":["T","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1448401685","alleles":["T","G"],"end":140499090,"feature_type":"variation","strand":1,"source":"dbSNP","start":140499090,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140499098,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499098,"clinical_significance":[],"seq_region_name":"7","id":"rs1795484263"},{"strand":1,"feature_type":"variation","end":140499099,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499099,"source":"dbSNP","id":"rs1795484283","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1454641072","clinical_significance":[],"end":140499100,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140499100,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795484315","end":140499101,"alleles":["GG","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140499100,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795484340","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499100,"source":"dbSNP","strand":1,"feature_type":"variation","end":140499104,"alleles":["GGTGC","-"]},{"seq_region_name":"7","id":"rs1217799771","clinical_significance":[],"start":140499101,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140499101,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499102,"feature_type":"variation","strand":1,"end":140499102,"alleles":["T","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585520767"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1335363925","end":140499103,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140499103,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499104,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140499104,"seq_region_name":"7","id":"rs1382661937","clinical_significance":[]},{"id":"rs1229723051","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499105,"source":"dbSNP","strand":1,"feature_type":"variation","end":140499105,"alleles":["A","C","G","T"]},{"id":"rs1795484475","seq_region_name":"7","clinical_significance":[],"alleles":["A","G"],"end":140499106,"strand":1,"feature_type":"variation","start":140499106,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140499108,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140499108,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1554454072"},{"id":"rs1795484515","seq_region_name":"7","clinical_significance":[],"end":140499114,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140499114,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140499115,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499115,"clinical_significance":[],"seq_region_name":"7","id":"rs1795484528"},{"seq_region_name":"7","id":"rs1172887503","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140499116,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499116,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140499122,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499122,"source":"dbSNP","seq_region_name":"7","id":"rs1795484555","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499123,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140499123,"clinical_significance":[],"id":"rs1795484577","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795484600","clinical_significance":[],"start":140499125,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C","G"],"end":140499125,"strand":1,"feature_type":"variation"},{"id":"rs1795484622","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499148,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140499148},{"seq_region_name":"7","id":"rs1795484638","clinical_significance":[],"strand":1,"feature_type":"variation","end":140499151,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499151,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499152,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140499152,"seq_region_name":"7","id":"rs1476999170","clinical_significance":[]},{"source":"dbSNP","start":140499153,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140499153,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1423179656","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1182806728","clinical_significance":[],"strand":1,"feature_type":"variation","end":140499162,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499162,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1272325854","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499163,"feature_type":"variation","strand":1,"end":140499163,"alleles":["T","C"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499169,"source":"dbSNP","strand":1,"feature_type":"variation","end":140499169,"alleles":["G","T"],"seq_region_name":"7","id":"rs1585520792","clinical_significance":[]},{"end":140499170,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140499170,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1484407077"},{"seq_region_name":"7","id":"rs957712029","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140499171,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499171,"source":"dbSNP"},{"seq_region_name":"7","id":"rs989656319","clinical_significance":[],"alleles":["GGG","GG"],"end":140499177,"strand":1,"feature_type":"variation","start":140499175,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs531891322","feature_type":"variation","strand":1,"end":140499179,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499179},{"clinical_significance":[],"seq_region_name":"7","id":"rs187312215","alleles":["A","G","T"],"end":140499183,"feature_type":"variation","strand":1,"source":"dbSNP","start":140499183,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1219917750","end":140499185,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140499185,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795484881","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499192,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140499192},{"seq_region_name":"7","id":"rs2130417851","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140499193,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499193,"source":"dbSNP"},{"start":140499194,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140499194,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1213646332","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1278879723","source":"dbSNP","start":140499196,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140499196,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1462319706","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499198,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140499198},{"alleles":["C","T"],"end":140499200,"strand":1,"feature_type":"variation","start":140499200,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795484984","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795485006","end":140499203,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140499203,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["G","A"],"end":140499204,"strand":1,"feature_type":"variation","start":140499204,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795485021","clinical_significance":[]},{"seq_region_name":"7","id":"rs1201199996","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499209,"source":"dbSNP","strand":1,"feature_type":"variation","end":140499209,"alleles":["A","C"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499211,"source":"dbSNP","strand":1,"feature_type":"variation","end":140499211,"alleles":["T","C"],"seq_region_name":"7","id":"rs1020733719","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499212,"feature_type":"variation","strand":1,"end":140499212,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1300837093"},{"seq_region_name":"7","id":"rs1465308532","clinical_significance":[],"alleles":["TT","T"],"end":140499222,"strand":1,"feature_type":"variation","start":140499221,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs966420779","clinical_significance":[],"start":140499223,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140499223,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499225,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140499225,"seq_region_name":"7","id":"rs1585520818","clinical_significance":[]},{"end":140499229,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140499229,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1400929217","clinical_significance":[]},{"start":140499231,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140499231,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795485178","clinical_significance":[]},{"alleles":["G","C"],"end":140499233,"strand":1,"feature_type":"variation","start":140499233,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795485200","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795485226","seq_region_name":"7","end":140499240,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140499240,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140499243,"alleles":["T","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499243,"clinical_significance":[],"seq_region_name":"7","id":"rs190905136"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1464066550","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140499244,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499244},{"end":140499252,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140499252,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1399850885","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795485330","clinical_significance":[],"end":140499257,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140499257,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795485356","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499259,"source":"dbSNP","strand":1,"feature_type":"variation","end":140499259,"alleles":["G","C"]},{"clinical_significance":[],"id":"rs368899050","seq_region_name":"7","end":140499262,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140499262,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1165682515","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499267,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140499267},{"end":140499268,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140499268,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795485431"},{"start":140499278,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140499278,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795485460","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499280,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140499280,"seq_region_name":"7","id":"rs1795485489","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795485518","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499286,"feature_type":"variation","strand":1,"end":140499286,"alleles":["A","G"]},{"source":"dbSNP","start":140499289,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140499289,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs927743182"},{"clinical_significance":[],"id":"rs1474951883","seq_region_name":"7","source":"dbSNP","start":140499290,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140499290,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795485612","clinical_significance":[],"end":140499299,"alleles":["CTGTCTCT","CT"],"strand":1,"feature_type":"variation","start":140499292,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1167624045","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["TGT","T"],"end":140499295,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499293,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499295,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TCTCT","TCT"],"end":140499299,"seq_region_name":"7","id":"rs57889896","clinical_significance":[]},{"seq_region_name":"7","id":"rs376788112","clinical_significance":[],"end":140499296,"alleles":["C","A","G"],"strand":1,"feature_type":"variation","start":140499296,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs2130417982","seq_region_name":"7","source":"dbSNP","start":140499296,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","-"],"end":140499296,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1440908128","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140499298,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499298,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1181617219","source":"dbSNP","start":140499298,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["CTATTG","-"],"end":140499303,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499299,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140499299,"seq_region_name":"7","id":"rs955295538","clinical_significance":[]},{"id":"rs1240566458","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140499299,"alleles":["-","TG"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499300,"source":"dbSNP"},{"seq_region_name":"7","id":"rs986651220","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499300,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140499300},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499302,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140499302,"seq_region_name":"7","id":"rs1795486010","clinical_significance":[]},{"end":140499303,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140499303,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1456035089"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1250444880","alleles":["A","G"],"end":140499304,"feature_type":"variation","strand":1,"source":"dbSNP","start":140499304,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563106300","feature_type":"variation","strand":1,"alleles":["ATTTATTTATTT","ATTTATTT","ATTTATTTATTTATTT"],"end":140499315,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499304},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499305,"feature_type":"variation","strand":1,"end":140499305,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs937959878"},{"seq_region_name":"7","id":"rs911011980","clinical_significance":[],"alleles":["T","G"],"end":140499307,"strand":1,"feature_type":"variation","start":140499307,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs990740301","end":140499312,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140499312,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140499315,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140499315,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1227529945","clinical_significance":[]},{"id":"rs942633395","seq_region_name":"7","clinical_significance":[],"alleles":["G","T"],"end":140499316,"strand":1,"feature_type":"variation","start":140499316,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795486292","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140499317,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499317},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499322,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140499322,"seq_region_name":"7","id":"rs1585520883","clinical_significance":[]},{"start":140499323,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140499323,"alleles":["A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs568664588","clinical_significance":[]},{"id":"rs1795486392","seq_region_name":"7","clinical_significance":[],"end":140499326,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140499326,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1795486421","seq_region_name":"7","clinical_significance":[],"alleles":["T","A","C"],"end":140499330,"strand":1,"feature_type":"variation","start":140499330,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs138362478","seq_region_name":"7","clinical_significance":[],"start":140499330,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140499342,"alleles":["TTATTTATTTATT","TTATT","TTATTTATT"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140499333,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140499333,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1585520891","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499338,"source":"dbSNP","strand":1,"feature_type":"variation","end":140499338,"alleles":["T","G"],"seq_region_name":"7","id":"rs925182188","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795486610","alleles":["T","A","C"],"end":140499339,"feature_type":"variation","strand":1,"source":"dbSNP","start":140499339,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499341,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140499341,"clinical_significance":[],"seq_region_name":"7","id":"rs1795486641"},{"clinical_significance":[],"seq_region_name":"7","id":"rs529561857","alleles":["T","C"],"end":140499342,"feature_type":"variation","strand":1,"source":"dbSNP","start":140499342,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1430459260","seq_region_name":"7","feature_type":"variation","strand":1,"end":140499343,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499343},{"seq_region_name":"7","id":"rs1795486726","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499354,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140499354},{"start":140499355,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140499355,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs1275115021","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140499362,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499362,"clinical_significance":[],"seq_region_name":"7","id":"rs1348345408"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1164595913","feature_type":"variation","strand":1,"end":140499364,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499364},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795487034","source":"dbSNP","start":140499365,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140499365,"alleles":["T","C"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140499366,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140499366,"alleles":["T","A","C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs10952704"},{"seq_region_name":"7","id":"rs1382727099","clinical_significance":[],"strand":1,"feature_type":"variation","end":140499373,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499373,"source":"dbSNP"},{"end":140499377,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140499377,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1177271082","clinical_significance":[]},{"alleles":["G","A"],"end":140499378,"feature_type":"variation","strand":1,"source":"dbSNP","start":140499378,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs934040059"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499381,"source":"dbSNP","strand":1,"feature_type":"variation","end":140499381,"alleles":["A","G"],"id":"rs1191259387","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795487223","source":"dbSNP","start":140499382,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140499382,"feature_type":"variation","strand":1},{"end":140499384,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140499384,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs779845410","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1221254982","source":"dbSNP","start":140499385,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140499385,"feature_type":"variation","strand":1},{"start":140499387,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140499387,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795487323","clinical_significance":[]},{"source":"dbSNP","start":140499389,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140499389,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795487345"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499390,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140499390,"clinical_significance":[],"id":"rs557365152","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795487389","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499392,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140499392},{"id":"rs1795487422","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140499394,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499394,"source":"dbSNP"},{"alleles":["C","T"],"end":140499395,"feature_type":"variation","strand":1,"source":"dbSNP","start":140499395,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs913355911"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795487462","source":"dbSNP","start":140499408,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140499408,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1261970963","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499413,"feature_type":"variation","strand":1,"end":140499413,"alleles":["A","C"]},{"alleles":["C","T"],"end":140499415,"feature_type":"variation","strand":1,"source":"dbSNP","start":140499415,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795487510"},{"end":140499420,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140499420,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795487536"},{"id":"rs180900407","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140499425,"strand":1,"feature_type":"variation","start":140499425,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs533908859","clinical_significance":[],"strand":1,"feature_type":"variation","end":140499426,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499426,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140499427,"alleles":["G","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499427,"clinical_significance":[],"seq_region_name":"7","id":"rs551864409"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499430,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140499430,"clinical_significance":[],"id":"rs1795487702","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585520943","end":140499441,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140499441,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs906003853","clinical_significance":[],"strand":1,"feature_type":"variation","end":140499443,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499443,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499446,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140499446,"clinical_significance":[],"seq_region_name":"7","id":"rs1585520947"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499447,"source":"dbSNP","strand":1,"feature_type":"variation","end":140499447,"alleles":["C","T"],"seq_region_name":"7","id":"rs1302140112","clinical_significance":[]},{"start":140499451,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140499451,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1001806908","clinical_significance":[]},{"clinical_significance":[],"id":"rs570460549","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140499453,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499453},{"id":"rs537738710","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140499455,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499455,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499457,"feature_type":"variation","strand":1,"alleles":["C","A","G","T"],"end":140499457,"clinical_significance":[],"seq_region_name":"7","id":"rs1199275229"},{"seq_region_name":"7","id":"rs898739867","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499458,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140499458},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795488010","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499460,"feature_type":"variation","strand":1,"alleles":["GTAGCTGG","G"],"end":140499467},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499461,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140499461,"clinical_significance":[],"seq_region_name":"7","id":"rs1795488035"},{"clinical_significance":[],"id":"rs1795488066","seq_region_name":"7","alleles":["C","T"],"end":140499464,"feature_type":"variation","strand":1,"source":"dbSNP","start":140499464,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795488087","clinical_significance":[],"alleles":["T","C"],"end":140499465,"strand":1,"feature_type":"variation","start":140499465,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1795488115","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140499466,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499466},{"clinical_significance":[],"id":"rs1481557681","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140499467,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499467},{"strand":1,"feature_type":"variation","end":140499473,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499473,"source":"dbSNP","seq_region_name":"7","id":"rs1419687722","clinical_significance":[]},{"alleles":["A","C"],"end":140499474,"feature_type":"variation","strand":1,"source":"dbSNP","start":140499474,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1378719222","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140499476,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499476,"source":"dbSNP","id":"rs1795488199","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140499477,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499477,"clinical_significance":[],"id":"rs1795488220","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499478,"source":"dbSNP","strand":1,"feature_type":"variation","end":140499478,"alleles":["G","T"],"seq_region_name":"7","id":"rs1174468173","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499482,"feature_type":"variation","strand":1,"end":140499482,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795488267"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1434342690","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140499484,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499484},{"clinical_significance":[],"seq_region_name":"7","id":"rs1264850087","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499489,"feature_type":"variation","strand":1,"end":140499489,"alleles":["T","A","C"]},{"start":140499492,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140499492,"alleles":["C","G"],"strand":1,"feature_type":"variation","id":"rs1795488305","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140499494,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499494,"clinical_significance":[],"seq_region_name":"7","id":"rs557135422"},{"clinical_significance":[],"id":"rs1795488340","seq_region_name":"7","end":140499497,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140499497,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1198186349","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499499,"source":"dbSNP","strand":1,"feature_type":"variation","end":140499499,"alleles":["A","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1488393498","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499503,"feature_type":"variation","strand":1,"alleles":["TTTGTATTTGTA","TTTGTA"],"end":140499514},{"clinical_significance":[],"seq_region_name":"7","id":"rs1428704801","source":"dbSNP","start":140499506,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140499506,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1214160671","clinical_significance":[],"end":140499507,"alleles":["T","A","G"],"strand":1,"feature_type":"variation","start":140499507,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140499508,"alleles":["A","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499508,"clinical_significance":[],"seq_region_name":"7","id":"rs1457826529"},{"feature_type":"variation","strand":1,"end":140499511,"alleles":["TTT","TT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499509,"clinical_significance":[],"seq_region_name":"7","id":"rs1256445549"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499512,"feature_type":"variation","strand":1,"end":140499512,"alleles":["G","T"],"clinical_significance":[],"id":"rs1235527249","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1310479238","clinical_significance":[],"start":140499518,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140499518,"alleles":["G","A","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1795488517","clinical_significance":[],"strand":1,"feature_type":"variation","end":140499523,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499523,"source":"dbSNP"},{"source":"dbSNP","start":140499524,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140499524,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795488537","seq_region_name":"7"},{"id":"rs556085061","seq_region_name":"7","clinical_significance":[],"end":140499525,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140499525,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795488564","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499527,"feature_type":"variation","strand":1,"end":140499527,"alleles":["T","C"]},{"alleles":["T","C","G"],"end":140499535,"strand":1,"feature_type":"variation","start":140499535,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795488582","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795488611","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140499536,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499536},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585520987","source":"dbSNP","start":140499543,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C","T"],"end":140499543,"feature_type":"variation","strand":1},{"alleles":["AA","A"],"end":140499544,"strand":1,"feature_type":"variation","start":140499543,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs71173204","clinical_significance":[]},{"source":"dbSNP","start":140499544,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G","T"],"end":140499544,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585521002"},{"start":140499545,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["GG","G"],"end":140499546,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130418290","clinical_significance":[]},{"end":140499546,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140499546,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795488760"},{"id":"rs1795488775","seq_region_name":"7","clinical_significance":[],"end":140499547,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140499547,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["C","T"],"end":140499552,"feature_type":"variation","strand":1,"source":"dbSNP","start":140499552,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130418297"},{"strand":1,"feature_type":"variation","end":140499554,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499554,"source":"dbSNP","seq_region_name":"7","id":"rs2130418300","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795488790","clinical_significance":[],"strand":1,"feature_type":"variation","end":140499555,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499555,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1219531016","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499561,"feature_type":"variation","strand":1,"end":140499561,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1342601838","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499563,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140499563},{"start":140499565,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140499565,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795488847","clinical_significance":[]},{"seq_region_name":"7","id":"rs539999981","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499568,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140499568},{"id":"rs1795488889","seq_region_name":"7","clinical_significance":[],"end":140499569,"alleles":["CA","-"],"strand":1,"feature_type":"variation","start":140499568,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795488908","source":"dbSNP","start":140499576,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140499576,"alleles":["C","A"],"feature_type":"variation","strand":1},{"alleles":["A","G","T"],"end":140499578,"feature_type":"variation","strand":1,"source":"dbSNP","start":140499578,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1399714008"},{"seq_region_name":"7","id":"rs1376439189","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499579,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140499579},{"seq_region_name":"7","id":"rs574393849","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499580,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140499580},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499581,"feature_type":"variation","strand":1,"end":140499581,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795488991"},{"seq_region_name":"7","id":"rs1795489008","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140499582,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499582,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["CC","CCCACC"],"end":140499584,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499583,"source":"dbSNP","seq_region_name":"7","id":"rs1795489030","clinical_significance":[]},{"source":"dbSNP","start":140499585,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140499585,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1400544519"},{"alleles":["C","T"],"end":140499586,"feature_type":"variation","strand":1,"source":"dbSNP","start":140499586,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs186317257","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs190296069","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140499587,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499587},{"id":"rs1034880097","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","C","T"],"end":140499588,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499588,"source":"dbSNP"},{"alleles":["C","T"],"end":140499589,"strand":1,"feature_type":"variation","start":140499589,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1191243332","clinical_significance":[]},{"end":140499590,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140499590,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1402732317","clinical_significance":[]},{"source":"dbSNP","start":140499595,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140499595,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1256817283"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499600,"feature_type":"variation","strand":1,"end":140499600,"alleles":["G","A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795489257"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499601,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140499601,"clinical_significance":[],"id":"rs1795489275","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795489300","end":140499603,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140499603,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1202147338","alleles":["A","C","G"],"end":140499604,"feature_type":"variation","strand":1,"source":"dbSNP","start":140499604,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["G","C","T"],"end":140499605,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499605,"source":"dbSNP","seq_region_name":"7","id":"rs144855098","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499606,"source":"dbSNP","strand":1,"feature_type":"variation","end":140499606,"alleles":["A","G"],"id":"rs182856996","seq_region_name":"7","clinical_significance":[]},{"start":140499613,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140499613,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1240523253","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1258939267","feature_type":"variation","strand":1,"end":140499614,"alleles":["T","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499614},{"clinical_significance":[],"id":"rs1795489452","seq_region_name":"7","alleles":["G","A","T"],"end":140499615,"feature_type":"variation","strand":1,"source":"dbSNP","start":140499615,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140499620,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499620,"source":"dbSNP","seq_region_name":"7","id":"rs1320278613","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795489475","source":"dbSNP","start":140499623,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140499623,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1276481035","clinical_significance":[],"end":140499626,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140499626,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs187489099","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499627,"source":"dbSNP","strand":1,"feature_type":"variation","end":140499627,"alleles":["G","A","T"]},{"id":"rs991038766","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140499642,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499642,"source":"dbSNP"},{"end":140499648,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140499648,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs925238435","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs576425712","feature_type":"variation","strand":1,"end":140499653,"alleles":["A","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499653},{"strand":1,"feature_type":"variation","alleles":["AAAAAAA","AAAAAA","AAAAAAAA"],"end":140499659,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499653,"source":"dbSNP","seq_region_name":"7","id":"rs1394848864","clinical_significance":[]},{"end":140499658,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140499658,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795489622","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140499659,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499659,"source":"dbSNP","seq_region_name":"7","id":"rs13225803","clinical_significance":[]},{"seq_region_name":"7","id":"rs117652947","clinical_significance":[],"start":140499660,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140499660,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1335577713","clinical_significance":[],"strand":1,"feature_type":"variation","end":140499669,"alleles":["TTTTTTTTTT","TTTTTTTTT","TTTTTTTTTTT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499660,"source":"dbSNP"},{"id":"rs918587365","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499661,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140499661},{"strand":1,"feature_type":"variation","end":140499663,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499663,"source":"dbSNP","id":"rs1795489771","seq_region_name":"7","clinical_significance":[]},{"end":140499669,"alleles":["T","TTTAAT"],"strand":1,"feature_type":"variation","start":140499669,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795489786","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795489804","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140499670,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499670},{"seq_region_name":"7","id":"rs1268444164","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140499672,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499672,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1368884963","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499674,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140499674},{"id":"rs2130418453","seq_region_name":"7","clinical_significance":[],"start":140499674,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","-"],"end":140499674,"strand":1,"feature_type":"variation"},{"end":140499675,"alleles":["A","AA"],"strand":1,"feature_type":"variation","start":140499675,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795489874","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs546311846","alleles":["AGAG","AG"],"end":140499678,"feature_type":"variation","strand":1,"source":"dbSNP","start":140499675,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795489917","source":"dbSNP","start":140499677,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140499677,"alleles":["A","G"],"feature_type":"variation","strand":1},{"end":140499678,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140499678,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs767891114"},{"id":"rs913192027","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499682,"source":"dbSNP","strand":1,"feature_type":"variation","end":140499682,"alleles":["C","G","T"]},{"clinical_significance":[],"id":"rs573758427","seq_region_name":"7","feature_type":"variation","strand":1,"end":140499683,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499683},{"clinical_significance":[],"seq_region_name":"7","id":"rs1459109796","end":140499688,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140499688,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795490020","source":"dbSNP","start":140499692,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140499692,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795490036","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499694,"source":"dbSNP","strand":1,"feature_type":"variation","end":140499694,"alleles":["C","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795490049","source":"dbSNP","start":140499695,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140499695,"alleles":["C","G"],"feature_type":"variation","strand":1},{"end":140499703,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140499703,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795490067","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795490077","clinical_significance":[],"alleles":["T","C"],"end":140499705,"strand":1,"feature_type":"variation","start":140499705,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140499706,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140499706,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs889974147","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140499709,"alleles":["G","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499709,"clinical_significance":[],"seq_region_name":"7","id":"rs1795490123"},{"id":"rs1795490135","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140499712,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499712,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs11764287","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499714,"feature_type":"variation","strand":1,"end":140499714,"alleles":["G","A","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499715,"feature_type":"variation","strand":1,"end":140499715,"alleles":["G","A","C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795490232"},{"alleles":["A","G"],"end":140499717,"strand":1,"feature_type":"variation","start":140499717,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1470103042","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130418511","source":"dbSNP","start":140499719,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140499719,"alleles":["C","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1164283901","alleles":["C","T"],"end":140499721,"feature_type":"variation","strand":1,"source":"dbSNP","start":140499721,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585521075","feature_type":"variation","strand":1,"end":140499723,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499723},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140499724,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499724,"clinical_significance":[],"id":"rs113988341","seq_region_name":"7"},{"start":140499727,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140499727,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1243063323","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499731,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140499731,"clinical_significance":[],"id":"rs2130418533","seq_region_name":"7"},{"source":"dbSNP","start":140499733,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140499733,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585521087"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140499735,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499735,"source":"dbSNP","seq_region_name":"7","id":"rs11766896","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795490413","seq_region_name":"7","source":"dbSNP","start":140499737,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140499737,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1310559526","feature_type":"variation","strand":1,"end":140499738,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499738},{"clinical_significance":[],"seq_region_name":"7","id":"rs1378527063","feature_type":"variation","strand":1,"end":140499739,"alleles":["A","C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499739},{"clinical_significance":[],"seq_region_name":"7","id":"rs1373737170","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499740,"feature_type":"variation","strand":1,"end":140499740,"alleles":["C","G","T"]},{"start":140499749,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140499749,"strand":1,"feature_type":"variation","id":"rs1302190100","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1055001673","clinical_significance":[],"alleles":["A","C","G"],"end":140499752,"strand":1,"feature_type":"variation","start":140499752,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1795490546","seq_region_name":"7","clinical_significance":[],"start":140499756,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140499756,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs545304426","feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140499757,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499757},{"strand":1,"feature_type":"variation","end":140499761,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499761,"source":"dbSNP","id":"rs1795490589","seq_region_name":"7","clinical_significance":[]},{"start":140499763,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140499763,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1384561880","clinical_significance":[]},{"id":"rs1795490620","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499765,"source":"dbSNP","strand":1,"feature_type":"variation","end":140499765,"alleles":["G","A","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1179138339","source":"dbSNP","start":140499767,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140499767,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795490654","alleles":["G","A"],"end":140499771,"feature_type":"variation","strand":1,"source":"dbSNP","start":140499771,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499772,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140499772,"clinical_significance":[],"seq_region_name":"7","id":"rs1392720753"},{"source":"dbSNP","start":140499773,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140499773,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795490686"},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140499780,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499780,"source":"dbSNP","seq_region_name":"7","id":"rs1795490701","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795490713","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499783,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140499783},{"seq_region_name":"7","id":"rs1304265780","clinical_significance":[],"strand":1,"feature_type":"variation","end":140499784,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499784,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130418597","source":"dbSNP","start":140499786,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140499786,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1010864607","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499788,"feature_type":"variation","strand":1,"end":140499788,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795490777","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499789,"feature_type":"variation","strand":1,"end":140499789,"alleles":["A","T"]},{"alleles":["A","G"],"end":140499792,"feature_type":"variation","strand":1,"source":"dbSNP","start":140499792,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1236481742"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795490807","alleles":["C","T"],"end":140499793,"feature_type":"variation","strand":1,"source":"dbSNP","start":140499793,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1181155367","source":"dbSNP","start":140499796,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140499796,"alleles":["G","A"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499797,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140499797,"clinical_significance":[],"id":"rs1020671438","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1452472591","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499806,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140499806},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499809,"source":"dbSNP","strand":1,"feature_type":"variation","end":140499809,"alleles":["C","A","G","T"],"id":"rs1245451435","seq_region_name":"7","clinical_significance":[]},{"id":"rs1046210540","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140499810,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499810,"source":"dbSNP"},{"end":140499815,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140499815,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs902167825"},{"clinical_significance":[],"id":"rs201959376","seq_region_name":"7","feature_type":"variation","strand":1,"end":140499820,"alleles":["T","A","C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499820},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499820,"source":"dbSNP","strand":1,"feature_type":"variation","end":140499830,"alleles":["TTTTTTTTTTT","TTTTTTTTTT","TTTTTTTTTTTT"],"seq_region_name":"7","id":"rs34339230","clinical_significance":[]},{"id":"rs927345075","seq_region_name":"7","clinical_significance":[],"start":140499824,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140499824,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs527378584","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140499829,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499829,"source":"dbSNP"},{"source":"dbSNP","start":140499829,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TT","AA"],"end":140499830,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs796218624"},{"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140499830,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499830,"clinical_significance":[],"seq_region_name":"7","id":"rs139673158"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1325062940","feature_type":"variation","strand":1,"end":140499831,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499831},{"seq_region_name":"7","id":"rs1795491162","clinical_significance":[],"strand":1,"feature_type":"variation","end":140499832,"alleles":["AA","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499831,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795491181","feature_type":"variation","strand":1,"end":140499842,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499842},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499846,"feature_type":"variation","strand":1,"end":140499846,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1012090997"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499847,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140499847,"clinical_significance":[],"id":"rs2130418654","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1364771639","clinical_significance":[],"start":140499848,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140499848,"alleles":["A","AA"],"strand":1,"feature_type":"variation"},{"start":140499848,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140499848,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795491220","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130418665","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499852,"source":"dbSNP","strand":1,"feature_type":"variation","end":140499854,"alleles":["TAA","-"]},{"seq_region_name":"7","id":"rs1158998304","clinical_significance":[],"start":140499855,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140499855,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795491272","feature_type":"variation","strand":1,"end":140499862,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499862},{"clinical_significance":[],"id":"rs898749755","seq_region_name":"7","feature_type":"variation","strand":1,"end":140499863,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499863},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499868,"source":"dbSNP","strand":1,"feature_type":"variation","end":140499868,"alleles":["T","C"],"seq_region_name":"7","id":"rs994791742","clinical_significance":[]},{"id":"rs1046739863","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140499869,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499869,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140499870,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499870,"clinical_significance":[],"seq_region_name":"7","id":"rs1795491333"},{"end":140499871,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140499871,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1158071793"},{"seq_region_name":"7","id":"rs1478362567","clinical_significance":[],"start":140499874,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140499874,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140499876,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499876,"source":"dbSNP","seq_region_name":"7","id":"rs1248695640","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1291380834","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140499880,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499880},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140499881,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499881,"source":"dbSNP","seq_region_name":"7","id":"rs1481096172","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140499888,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499888,"clinical_significance":[],"id":"rs1017142490","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795491476","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499892,"source":"dbSNP","strand":1,"feature_type":"variation","end":140499892,"alleles":["C","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499893,"feature_type":"variation","strand":1,"end":140499893,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795491494"},{"seq_region_name":"7","id":"rs1219245174","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499900,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140499900},{"seq_region_name":"7","id":"rs1197733659","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499903,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140499903},{"clinical_significance":[],"seq_region_name":"7","id":"rs1248515077","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499905,"feature_type":"variation","strand":1,"end":140499905,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1284116319","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499908,"feature_type":"variation","strand":1,"end":140499908,"alleles":["C","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499911,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140499911,"seq_region_name":"7","id":"rs374173683","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs111408805","feature_type":"variation","strand":1,"end":140499912,"alleles":["G","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499912},{"seq_region_name":"7","id":"rs1795492019","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499920,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140499920},{"clinical_significance":[],"id":"rs972619541","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499921,"feature_type":"variation","strand":1,"end":140499921,"alleles":["C","A"]},{"end":140499924,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140499924,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1298650371"},{"clinical_significance":[],"seq_region_name":"7","id":"rs371241776","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499927,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140499927},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499928,"feature_type":"variation","strand":1,"end":140499928,"alleles":["C","A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795492127"},{"seq_region_name":"7","id":"rs1795492153","clinical_significance":[],"start":140499933,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140499933,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140499940,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140499940,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795492161"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140499943,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499943,"source":"dbSNP","seq_region_name":"7","id":"rs1795492185","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140499952,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499952,"source":"dbSNP","seq_region_name":"7","id":"rs1343376522","clinical_significance":[]},{"end":140499954,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140499954,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1018007001","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795492245","end":140499957,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140499957,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140499959,"alleles":["T","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499959,"clinical_significance":[],"seq_region_name":"7","id":"rs1563106420"},{"seq_region_name":"7","id":"rs1415139976","clinical_significance":[],"end":140499963,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140499963,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1427402599","seq_region_name":"7","clinical_significance":[],"alleles":["T","G"],"end":140499965,"strand":1,"feature_type":"variation","start":140499965,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["G","A"],"end":140499966,"strand":1,"feature_type":"variation","start":140499966,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1443218045","clinical_significance":[]},{"source":"dbSNP","start":140499967,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140499967,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1174352728","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499969,"feature_type":"variation","strand":1,"end":140499969,"alleles":["A","G"],"clinical_significance":[],"id":"rs1480271294","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499970,"source":"dbSNP","strand":1,"feature_type":"variation","end":140499970,"alleles":["T","C"],"seq_region_name":"7","id":"rs1795492409","clinical_significance":[]},{"id":"rs1424523416","seq_region_name":"7","clinical_significance":[],"end":140499971,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140499971,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499972,"feature_type":"variation","strand":1,"end":140499972,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1196317160"},{"alleles":["T","C"],"end":140499974,"strand":1,"feature_type":"variation","start":140499974,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1487485915","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499975,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140499975,"seq_region_name":"7","id":"rs1242083703","clinical_significance":[]},{"alleles":["CCCCCC","CCCCC"],"end":140499980,"feature_type":"variation","strand":1,"source":"dbSNP","start":140499975,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795492560"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795492587","source":"dbSNP","start":140499976,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140499976,"alleles":["C","T"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499979,"feature_type":"variation","strand":1,"end":140499979,"alleles":["C","A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs918613579"},{"seq_region_name":"7","id":"rs1795492649","clinical_significance":[],"start":140499980,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140499980,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585521232","source":"dbSNP","start":140499981,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140499981,"alleles":["T","C"],"feature_type":"variation","strand":1},{"id":"rs955354554","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499982,"source":"dbSNP","strand":1,"feature_type":"variation","end":140499982,"alleles":["C","G","T"]},{"end":140499983,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140499983,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795492755","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585521240","clinical_significance":[],"start":140499984,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140499984,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"start":140499986,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","G","T"],"end":140499986,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1201222343","clinical_significance":[]},{"start":140499987,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C"],"end":140499987,"strand":1,"feature_type":"variation","id":"rs1463199763","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499987,"source":"dbSNP","strand":1,"feature_type":"variation","end":140499988,"alleles":["GA","-"],"seq_region_name":"7","id":"rs2130418780","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585521244","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140499988,"feature_type":"variation","strand":1,"end":140499988,"alleles":["A","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1220261043","source":"dbSNP","start":140499989,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140499989,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795492951","clinical_significance":[],"start":140499990,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140499990,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140499991,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499991,"source":"dbSNP","seq_region_name":"7","id":"rs1795492972","clinical_significance":[]},{"end":140499992,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140499992,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795492998","clinical_significance":[]},{"id":"rs1585521253","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140499993,"source":"dbSNP","strand":1,"feature_type":"variation","end":140499993,"alleles":["A","C"]},{"source":"dbSNP","start":140500006,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140500006,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795493049"},{"id":"rs1296028572","seq_region_name":"7","clinical_significance":[],"start":140500007,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140500014,"alleles":["TATTATTA","TATTA"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs986737616","end":140500010,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140500010,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500011,"feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140500011,"clinical_significance":[],"seq_region_name":"7","id":"rs1395221827"},{"feature_type":"variation","strand":1,"end":140500012,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500012,"clinical_significance":[],"seq_region_name":"7","id":"rs1396106694"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130418813","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500017,"feature_type":"variation","strand":1,"end":140500021,"alleles":["AGAGA","AGA"]},{"seq_region_name":"7","id":"rs911321631","clinical_significance":[],"start":140500018,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140500018,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500019,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140500019,"id":"rs1338669519","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795493325","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500024,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140500024},{"id":"rs1380465755","seq_region_name":"7","clinical_significance":[],"end":140500025,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140500025,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140500026,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140500026,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs537401837","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795493393","clinical_significance":[],"strand":1,"feature_type":"variation","end":140500027,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500027,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140500032,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500032,"clinical_significance":[],"id":"rs1585521270","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795493453","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500033,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140500033},{"alleles":["A","G"],"end":140500034,"feature_type":"variation","strand":1,"source":"dbSNP","start":140500034,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795493492","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1334794402","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500035,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140500035},{"id":"rs1795493558","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140500041,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500041,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1469305950","clinical_significance":[],"start":140500043,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140500043,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1795493635","clinical_significance":[],"start":140500045,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140500045,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"start":140500047,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140500047,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795493684","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795493719","feature_type":"variation","strand":1,"end":140500052,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500052},{"seq_region_name":"7","id":"rs1401334049","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140500053,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500053,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs139151202","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140500054,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500054},{"clinical_significance":[],"seq_region_name":"7","id":"rs1000694646","end":140500058,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140500058,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140500059,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140500059,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1563106448","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1032096597","feature_type":"variation","strand":1,"end":140500064,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500064},{"seq_region_name":"7","id":"rs188807048","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140500065,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500065,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500068,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140500068,"clinical_significance":[],"seq_region_name":"7","id":"rs1419317213"},{"feature_type":"variation","strand":1,"end":140500069,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500069,"clinical_significance":[],"id":"rs988437678","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140500077,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500077,"source":"dbSNP","id":"rs1795494041","seq_region_name":"7","clinical_significance":[]},{"alleles":["CC","C"],"end":140500079,"feature_type":"variation","strand":1,"source":"dbSNP","start":140500078,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795494078","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500091,"feature_type":"variation","strand":1,"end":140500091,"alleles":["C","T"],"clinical_significance":[],"id":"rs942743797","seq_region_name":"7"},{"end":140500092,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140500092,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1474095437","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140500097,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500097,"source":"dbSNP","seq_region_name":"7","id":"rs1795494177","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1241762777","feature_type":"variation","strand":1,"end":140500098,"alleles":["G","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500098},{"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140500099,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500099,"clinical_significance":[],"seq_region_name":"7","id":"rs1795494245"},{"strand":1,"feature_type":"variation","end":140500100,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500100,"source":"dbSNP","seq_region_name":"7","id":"rs1181227682","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs913252784","source":"dbSNP","start":140500102,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140500102,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs971829482","alleles":["G","A","T"],"end":140500104,"feature_type":"variation","strand":1,"source":"dbSNP","start":140500104,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs914722395","clinical_significance":[],"strand":1,"feature_type":"variation","end":140500109,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500109,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795494398","clinical_significance":[],"start":140500112,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140500112,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1249830779","seq_region_name":"7","feature_type":"variation","strand":1,"end":140500113,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500113},{"clinical_significance":[],"seq_region_name":"7","id":"rs192523033","alleles":["G","A"],"end":140500114,"feature_type":"variation","strand":1,"source":"dbSNP","start":140500114,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140500121,"alleles":["AGTCA","AGTCAGTCA"],"strand":1,"feature_type":"variation","start":140500117,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1228608647","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795494508","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500122,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140500122},{"seq_region_name":"7","id":"rs1795494542","clinical_significance":[],"start":140500123,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140500123,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"id":"rs759770620","seq_region_name":"7","clinical_significance":[],"end":140500127,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140500127,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140500130,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500130,"source":"dbSNP","seq_region_name":"7","id":"rs1795494608","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["CC","C"],"end":140500133,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500132,"clinical_significance":[],"seq_region_name":"7","id":"rs1041974442"},{"end":140500136,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140500136,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795494665","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500138,"feature_type":"variation","strand":1,"end":140500138,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs981456849"},{"feature_type":"variation","strand":1,"end":140500144,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500144,"clinical_significance":[],"seq_region_name":"7","id":"rs1795494718"},{"clinical_significance":[],"id":"rs1795494753","seq_region_name":"7","feature_type":"variation","strand":1,"end":140500146,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500146},{"clinical_significance":[],"id":"rs1795494782","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500147,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140500147},{"seq_region_name":"7","id":"rs1795494806","clinical_significance":[],"strand":1,"feature_type":"variation","end":140500149,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500149,"source":"dbSNP"},{"id":"rs1795494835","seq_region_name":"7","clinical_significance":[],"start":140500150,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140500150,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500153,"source":"dbSNP","strand":1,"feature_type":"variation","end":140500153,"alleles":["G","C"],"seq_region_name":"7","id":"rs1312772442","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500156,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140500156,"clinical_significance":[],"seq_region_name":"7","id":"rs927398974"},{"seq_region_name":"7","id":"rs2130418995","clinical_significance":[],"end":140500157,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140500157,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["C","A"],"end":140500161,"strand":1,"feature_type":"variation","start":140500161,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs2130418996","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500162,"feature_type":"variation","strand":1,"end":140500162,"alleles":["A","G"],"clinical_significance":[],"id":"rs2130419001","seq_region_name":"7"},{"source":"dbSNP","start":140500167,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140500167,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs375461227","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1333426646","seq_region_name":"7","feature_type":"variation","strand":1,"end":140500170,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500170},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795495030","alleles":["A","G"],"end":140500172,"feature_type":"variation","strand":1,"source":"dbSNP","start":140500172,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795495061","clinical_significance":[],"alleles":["C","G","T"],"end":140500173,"strand":1,"feature_type":"variation","start":140500173,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795495110","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500178,"feature_type":"variation","strand":1,"end":140500178,"alleles":["A","G"]},{"end":140500179,"alleles":["G","C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140500179,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs868739251"},{"seq_region_name":"7","id":"rs1795495185","clinical_significance":[],"start":140500180,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140500180,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1585521303","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140500182,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500182,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795495262","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500185,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140500185},{"strand":1,"feature_type":"variation","end":140500191,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500191,"source":"dbSNP","id":"rs568723730","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795495338","end":140500193,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140500193,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140500197,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140500197,"alleles":["A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795495366","clinical_significance":[]},{"start":140500200,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140500200,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs56237987","clinical_significance":[]},{"source":"dbSNP","start":140500202,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140500202,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1354151672"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140500206,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500206,"clinical_significance":[],"seq_region_name":"7","id":"rs2130419034"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795495445","end":140500208,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140500208,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs572240835","seq_region_name":"7","clinical_significance":[],"start":140500210,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140500210,"strand":1,"feature_type":"variation"},{"alleles":["GGG","GG"],"end":140500213,"feature_type":"variation","strand":1,"source":"dbSNP","start":140500211,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795495513"},{"source":"dbSNP","start":140500212,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140500212,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1165930975","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795495556","source":"dbSNP","start":140500217,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140500217,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1407373036","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500220,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140500220},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500236,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140500236,"clinical_significance":[],"id":"rs1383946136","seq_region_name":"7"},{"alleles":["G","A"],"end":140500240,"feature_type":"variation","strand":1,"source":"dbSNP","start":140500240,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1163460727","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140500241,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500241,"source":"dbSNP","id":"rs1795495684","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140500242,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500242,"clinical_significance":[],"seq_region_name":"7","id":"rs1460394653"},{"id":"rs1795495763","seq_region_name":"7","clinical_significance":[],"alleles":["A","G"],"end":140500248,"strand":1,"feature_type":"variation","start":140500248,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795495799","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500249,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140500249},{"start":140500254,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140500254,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795495829","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500261,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140500261,"id":"rs1585521323","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795495906","end":140500262,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140500262,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795495933","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140500263,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500263,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140500266,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500266,"clinical_significance":[],"seq_region_name":"7","id":"rs1183442532"},{"seq_region_name":"7","id":"rs539543024","clinical_significance":[],"strand":1,"feature_type":"variation","end":140500268,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500268,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1178427083","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500269,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140500269},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500272,"feature_type":"variation","strand":1,"end":140500272,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs78519862"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563106472","alleles":["ACCCCTTC","-"],"end":140500280,"feature_type":"variation","strand":1,"source":"dbSNP","start":140500273,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140500274,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500274,"source":"dbSNP","seq_region_name":"7","id":"rs930261105","clinical_significance":[]},{"clinical_significance":[],"id":"rs1222061634","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500282,"feature_type":"variation","strand":1,"end":140500282,"alleles":["A","G"]},{"clinical_significance":[],"id":"rs1012409096","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500287,"feature_type":"variation","strand":1,"end":140500287,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs1289290032","clinical_significance":[],"start":140500289,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140500289,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1795496238","clinical_significance":[],"end":140500290,"alleles":["G","-"],"strand":1,"feature_type":"variation","start":140500290,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1585521352","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140500292,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500292},{"end":140500294,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140500294,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1016804079"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130419111","end":140500295,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140500295,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140500299,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140500299,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795496324","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500302,"feature_type":"variation","strand":1,"end":140500302,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1311638430"},{"feature_type":"variation","strand":1,"alleles":["T","TT"],"end":140500303,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500303,"clinical_significance":[],"seq_region_name":"7","id":"rs1354315939"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500305,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140500305,"clinical_significance":[],"id":"rs1795496414","seq_region_name":"7"},{"id":"rs1795496444","seq_region_name":"7","clinical_significance":[],"end":140500306,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140500306,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795496499","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140500307,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500307,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1389675362","seq_region_name":"7","alleles":["A","T"],"end":140500309,"feature_type":"variation","strand":1,"source":"dbSNP","start":140500309,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500313,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140500313,"clinical_significance":[],"seq_region_name":"7","id":"rs1372885906"},{"start":140500318,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140500318,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1294288372","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140500321,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500321,"source":"dbSNP","id":"rs1372115389","seq_region_name":"7","clinical_significance":[]},{"end":140500322,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140500322,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1364140933","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1047784944","clinical_significance":[],"start":140500324,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140500324,"strand":1,"feature_type":"variation"},{"id":"rs1585521366","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500332,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140500332},{"alleles":["T","C"],"end":140500333,"strand":1,"feature_type":"variation","start":140500333,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1420896723","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140500334,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500334,"clinical_significance":[],"seq_region_name":"7","id":"rs1469915763"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500335,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140500335,"seq_region_name":"7","id":"rs962852117","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140500336,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500336,"clinical_significance":[],"id":"rs1795496817","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs891363988","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500337,"feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140500337},{"seq_region_name":"7","id":"rs1795496870","clinical_significance":[],"end":140500340,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140500340,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1416742245","source":"dbSNP","start":140500343,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140500343,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500344,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140500344,"seq_region_name":"7","id":"rs1795496926","clinical_significance":[]},{"seq_region_name":"7","id":"rs755615188","clinical_significance":[],"strand":1,"feature_type":"variation","end":140500349,"alleles":["A","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500349,"source":"dbSNP"},{"start":140500350,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140500350,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795497004","clinical_significance":[]},{"clinical_significance":[],"id":"rs1490732842","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500352,"feature_type":"variation","strand":1,"end":140500352,"alleles":["A","T"]},{"alleles":["TTTTTTTTTTT","TTTTTTTTTT","TTTTTTTTTTTT"],"end":140500363,"feature_type":"variation","strand":1,"source":"dbSNP","start":140500353,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs994066143"},{"seq_region_name":"7","id":"rs1177997826","clinical_significance":[],"end":140500356,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140500356,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs184528673","feature_type":"variation","strand":1,"end":140500363,"alleles":["T","A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500363},{"seq_region_name":"7","id":"rs115856412","clinical_significance":[],"start":140500364,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140500364,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1039342719","seq_region_name":"7","feature_type":"variation","strand":1,"end":140500365,"alleles":["A","C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500365},{"clinical_significance":[],"id":"rs1363893218","seq_region_name":"7","source":"dbSNP","start":140500366,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140500366,"alleles":["A","T"],"feature_type":"variation","strand":1},{"end":140500372,"alleles":["TTTTTT","TTTTTTT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140500367,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795497343","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1316371241","source":"dbSNP","start":140500373,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140500373,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs899594502","clinical_significance":[],"start":140500376,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G","T"],"end":140500376,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1302030480","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140500378,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500378,"source":"dbSNP"},{"end":140500379,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140500379,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795497436"},{"clinical_significance":[],"id":"rs1795497479","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140500380,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500380},{"source":"dbSNP","start":140500381,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140500381,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1000537446","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1221202050","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500385,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140500385},{"alleles":["G","A","C"],"end":140500386,"strand":1,"feature_type":"variation","start":140500386,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs539368646","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs892272837","seq_region_name":"7","end":140500397,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140500397,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140500398,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500398,"clinical_significance":[],"seq_region_name":"7","id":"rs1795497659"},{"alleles":["A","G"],"end":140500399,"feature_type":"variation","strand":1,"source":"dbSNP","start":140500399,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1380281657"},{"end":140500401,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140500401,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1293763939","seq_region_name":"7","clinical_significance":[]},{"id":"rs1287591926","seq_region_name":"7","clinical_significance":[],"start":140500404,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140500404,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs964200191","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500405,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140500405},{"clinical_significance":[],"id":"rs1009386371","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140500408,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500408},{"clinical_significance":[],"seq_region_name":"7","id":"rs1481254332","end":140500409,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140500409,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140500412,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140500412,"strand":1,"feature_type":"variation","id":"rs1795497944","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140500413,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140500413,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1265082601","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1321428574","end":140500414,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140500414,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["C","A","G","T"],"end":140500418,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500418,"clinical_significance":[],"id":"rs144048059","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795498158","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500419,"source":"dbSNP","strand":1,"feature_type":"variation","end":140500419,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs970666908","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140500421,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500421},{"alleles":["A","C"],"end":140500422,"strand":1,"feature_type":"variation","start":140500422,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795498217","clinical_significance":[]},{"source":"dbSNP","start":140500423,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140500423,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs981851418","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795498279","source":"dbSNP","start":140500424,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140500424,"alleles":["T","C"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140500426,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500426,"clinical_significance":[],"seq_region_name":"7","id":"rs1203358398"},{"alleles":["C","T"],"end":140500427,"feature_type":"variation","strand":1,"source":"dbSNP","start":140500427,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1485489686","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500436,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140500436,"seq_region_name":"7","id":"rs1585521443","clinical_significance":[]},{"alleles":["C","T"],"end":140500437,"strand":1,"feature_type":"variation","start":140500437,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795498387","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795498413","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500438,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140500438},{"clinical_significance":[],"seq_region_name":"7","id":"rs1256724380","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500438,"feature_type":"variation","strand":1,"end":140500441,"alleles":["CTCT","CT"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795498469","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500439,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140500439},{"source":"dbSNP","start":140500440,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140500440,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs188219418"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795498555","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500441,"feature_type":"variation","strand":1,"end":140500441,"alleles":["T","C"]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140500442,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500442,"source":"dbSNP","seq_region_name":"7","id":"rs1795498580","clinical_significance":[]},{"seq_region_name":"7","id":"rs958789116","clinical_significance":[],"start":140500443,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140500443,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1282830886","clinical_significance":[],"start":140500444,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140500444,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1585521452","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140500446,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500446},{"clinical_significance":[],"id":"rs1185122238","seq_region_name":"7","source":"dbSNP","start":140500447,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140500447,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs974129413","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500448,"feature_type":"variation","strand":1,"end":140500448,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1328602568","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140500449,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500449},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500451,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140500451,"clinical_significance":[],"seq_region_name":"7","id":"rs1795498746"},{"feature_type":"variation","strand":1,"end":140500452,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500452,"clinical_significance":[],"seq_region_name":"7","id":"rs1795498765"},{"start":140500458,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140500458,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs928878733","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140500459,"alleles":["G","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500459,"clinical_significance":[],"seq_region_name":"7","id":"rs375276905"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500464,"source":"dbSNP","strand":1,"feature_type":"variation","end":140500464,"alleles":["T","C"],"id":"rs1795498862","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs919989631","clinical_significance":[],"strand":1,"feature_type":"variation","end":140500465,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500465,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs938874655","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500467,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140500467},{"source":"dbSNP","start":140500471,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140500471,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795498910","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795498939","feature_type":"variation","strand":1,"end":140500472,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500472},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795498958","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140500475,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500475},{"source":"dbSNP","start":140500476,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140500476,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1426611047"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500479,"source":"dbSNP","strand":1,"feature_type":"variation","end":140500479,"alleles":["C","T"],"seq_region_name":"7","id":"rs1795499006","clinical_significance":[]},{"seq_region_name":"7","id":"rs559681322","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140500480,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500480,"source":"dbSNP"},{"alleles":["G","A"],"end":140500481,"strand":1,"feature_type":"variation","start":140500481,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs572707398","clinical_significance":[]},{"seq_region_name":"7","id":"rs912846967","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140500483,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500483,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1232528832","clinical_significance":[],"start":140500484,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140500484,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140500487,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500487,"source":"dbSNP","seq_region_name":"7","id":"rs2130419388","clinical_significance":[]},{"end":140500491,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140500491,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1346869687","seq_region_name":"7"},{"seq_region_name":"7","id":"rs894794158","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500492,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140500492},{"end":140500493,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140500493,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs533619905","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500496,"feature_type":"variation","strand":1,"end":140500496,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795499312"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140500502,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500502,"clinical_significance":[],"seq_region_name":"7","id":"rs1795499339"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500504,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140500504,"clinical_significance":[],"seq_region_name":"7","id":"rs1451476418"},{"source":"dbSNP","start":140500505,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140500505,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1190742420"},{"start":140500505,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["GCCACCACGTCCGGC","GC"],"end":140500519,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795499405","clinical_significance":[]},{"clinical_significance":[],"id":"rs1585521488","seq_region_name":"7","end":140500508,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140500508,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140500510,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140500510,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795499456"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1427918423","feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140500512,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500512},{"id":"rs944265000","seq_region_name":"7","clinical_significance":[],"start":140500513,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140500513,"strand":1,"feature_type":"variation"},{"alleles":["C","G","T"],"end":140500516,"strand":1,"feature_type":"variation","start":140500516,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs551684967","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500517,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140500517,"clinical_significance":[],"id":"rs1038513254","seq_region_name":"7"},{"alleles":["A","G"],"end":140500521,"feature_type":"variation","strand":1,"source":"dbSNP","start":140500521,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs898229412","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1199557298","clinical_significance":[],"alleles":["A","C"],"end":140500522,"strand":1,"feature_type":"variation","start":140500522,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1795499724","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500523,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140500523},{"clinical_significance":[],"id":"rs1795499750","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140500524,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500524},{"clinical_significance":[],"seq_region_name":"7","id":"rs868405507","feature_type":"variation","strand":1,"end":140500531,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500531},{"seq_region_name":"7","id":"rs1795499806","clinical_significance":[],"strand":1,"feature_type":"variation","end":140500531,"alleles":["-","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500532,"source":"dbSNP"},{"end":140500543,"alleles":["TTTTTTTTTTTT","TTTTTTTTTTT","TTTTTTTTTTTTT"],"strand":1,"feature_type":"variation","start":140500532,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs993976129","clinical_significance":[]},{"seq_region_name":"7","id":"rs1563106540","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140500541,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500541,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1025399127","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500543,"source":"dbSNP","strand":1,"feature_type":"variation","end":140500543,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795499946","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500544,"feature_type":"variation","strand":1,"end":140500544,"alleles":["C","T"]},{"id":"rs1795499986","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140500546,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500546,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1285412485","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500549,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140500549},{"clinical_significance":[],"id":"rs1795500026","seq_region_name":"7","alleles":["T","G"],"end":140500550,"feature_type":"variation","strand":1,"source":"dbSNP","start":140500550,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795500056","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500552,"source":"dbSNP","strand":1,"feature_type":"variation","end":140500552,"alleles":["G","T"]},{"id":"rs1317721419","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500554,"source":"dbSNP","strand":1,"feature_type":"variation","end":140500554,"alleles":["G","A","T"]},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140500555,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500555,"source":"dbSNP","seq_region_name":"7","id":"rs1795500112","clinical_significance":[]},{"clinical_significance":[],"id":"rs1454149792","seq_region_name":"7","end":140500556,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140500556,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795500184","alleles":["C","A"],"end":140500560,"feature_type":"variation","strand":1,"source":"dbSNP","start":140500560,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1343794708","clinical_significance":[],"alleles":["T","C"],"end":140500561,"strand":1,"feature_type":"variation","start":140500561,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1379994546","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140500562,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500562,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795500243","source":"dbSNP","start":140500568,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140500568,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585521525","source":"dbSNP","start":140500570,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140500570,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795500292","clinical_significance":[],"start":140500574,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140500574,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1335468840","clinical_significance":[],"start":140500581,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140500581,"strand":1,"feature_type":"variation"},{"end":140500585,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140500585,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795500334","clinical_significance":[]},{"seq_region_name":"7","id":"rs1447142376","clinical_significance":[],"start":140500589,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140500589,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563106546","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500590,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140500590},{"source":"dbSNP","start":140500592,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140500592,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795500444"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500593,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140500593,"seq_region_name":"7","id":"rs1398181997","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs891045895","source":"dbSNP","start":140500599,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140500599,"alleles":["C","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795500507","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500606,"feature_type":"variation","strand":1,"end":140500606,"alleles":["C","T"]},{"feature_type":"variation","strand":1,"end":140500609,"alleles":["G","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500609,"clinical_significance":[],"seq_region_name":"7","id":"rs1008096881"},{"start":140500611,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A","C"],"end":140500611,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs191882955","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795500614","clinical_significance":[],"alleles":["C","T"],"end":140500613,"strand":1,"feature_type":"variation","start":140500613,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140500614,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140500614,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795500635","clinical_significance":[]},{"alleles":["C","T"],"end":140500615,"strand":1,"feature_type":"variation","start":140500615,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130419539","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795500654","clinical_significance":[],"start":140500617,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140500617,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500620,"feature_type":"variation","strand":1,"end":140500620,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795500678"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140500623,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500623,"source":"dbSNP","seq_region_name":"7","id":"rs531322233","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140500626,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500626,"clinical_significance":[],"seq_region_name":"7","id":"rs1795500732"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1369019269","source":"dbSNP","start":140500627,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140500627,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1165437376","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500630,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140500630},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500631,"source":"dbSNP","strand":1,"feature_type":"variation","end":140500631,"alleles":["A","G"],"seq_region_name":"7","id":"rs1795500833","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795500865","clinical_significance":[],"start":140500636,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140500636,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs2130419564","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500638,"source":"dbSNP","strand":1,"feature_type":"variation","end":140500638,"alleles":["C","T"]},{"id":"rs1795500896","seq_region_name":"7","clinical_significance":[],"end":140500639,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140500639,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140500641,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140500641,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795500928","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795500953","clinical_significance":[],"start":140500642,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140500642,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140500644,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500644,"source":"dbSNP","seq_region_name":"7","id":"rs936445525","clinical_significance":[]},{"seq_region_name":"7","id":"rs1053494015","clinical_significance":[],"end":140500646,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140500646,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs549338598","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500650,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140500650},{"seq_region_name":"7","id":"rs1795501054","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500651,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140500651},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795501079","feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140500652,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500652},{"seq_region_name":"7","id":"rs1795501106","clinical_significance":[],"start":140500653,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140500653,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140500655,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500655,"source":"dbSNP","seq_region_name":"7","id":"rs1439778123","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795501152","feature_type":"variation","strand":1,"end":140500656,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500656},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500661,"feature_type":"variation","strand":1,"end":140500661,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795501180"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140500662,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500662,"source":"dbSNP","seq_region_name":"7","id":"rs2130419599","clinical_significance":[]},{"source":"dbSNP","start":140500663,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140500663,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1022140218","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140500665,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500665,"clinical_significance":[],"seq_region_name":"7","id":"rs1195613986"},{"id":"rs1357453543","seq_region_name":"7","clinical_significance":[],"start":140500672,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140500672,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs202068008","source":"dbSNP","start":140500673,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140500673,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1244485578","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500674,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140500674},{"start":140500676,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140500676,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795501330","clinical_significance":[]},{"id":"rs1795501348","seq_region_name":"7","clinical_significance":[],"alleles":["C","G"],"end":140500678,"strand":1,"feature_type":"variation","start":140500678,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140500681,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140500681,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795501370","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795501392","source":"dbSNP","start":140500687,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140500687,"alleles":["T","G"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140500688,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500688,"source":"dbSNP","seq_region_name":"7","id":"rs1359334020","clinical_significance":[]},{"seq_region_name":"7","id":"rs1313826406","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500692,"source":"dbSNP","strand":1,"feature_type":"variation","end":140500692,"alleles":["T","C"]},{"feature_type":"variation","strand":1,"end":140500694,"alleles":["A","C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500694,"clinical_significance":[],"seq_region_name":"7","id":"rs1585521564"},{"strand":1,"feature_type":"variation","end":140500695,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500695,"source":"dbSNP","seq_region_name":"7","id":"rs1024769216","clinical_significance":[]},{"seq_region_name":"7","id":"rs1442216353","clinical_significance":[],"start":140500695,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140500703,"alleles":["TTTTTTTGT","TTTTTTTGTTTTTTTGT"],"strand":1,"feature_type":"variation"},{"alleles":["G","T"],"end":140500702,"feature_type":"variation","strand":1,"source":"dbSNP","start":140500702,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1326399149"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795501646","alleles":["A","T"],"end":140500708,"feature_type":"variation","strand":1,"source":"dbSNP","start":140500708,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795501672","alleles":["G","C"],"end":140500714,"feature_type":"variation","strand":1,"source":"dbSNP","start":140500714,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs906447714","seq_region_name":"7","end":140500716,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140500716,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500716,"source":"dbSNP","strand":1,"feature_type":"variation","end":140500728,"alleles":["CAGGGTTTCACCA","CA"],"seq_region_name":"7","id":"rs1795501724","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795501745","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500718,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140500718},{"end":140500719,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140500719,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1366011792","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500720,"feature_type":"variation","strand":1,"end":140500720,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795501795"},{"id":"rs1795501818","seq_region_name":"7","clinical_significance":[],"start":140500722,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140500722,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1304715500","clinical_significance":[],"start":140500723,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140500723,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500729,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140500729,"seq_region_name":"7","id":"rs2130419667","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140500731,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500731,"clinical_significance":[],"id":"rs1795501862","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585521574","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500732,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140500732},{"alleles":["C","G","T"],"end":140500735,"strand":1,"feature_type":"variation","start":140500735,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1490599650","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500738,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140500738,"clinical_significance":[],"seq_region_name":"7","id":"rs1224328069"},{"seq_region_name":"7","id":"rs1002090189","clinical_significance":[],"strand":1,"feature_type":"variation","end":140500745,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500745,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1384457701","end":140500748,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140500748,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500751,"source":"dbSNP","strand":1,"feature_type":"variation","end":140500751,"alleles":["C","G"],"id":"rs1159337455","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500752,"source":"dbSNP","strand":1,"feature_type":"variation","end":140500752,"alleles":["T","C"],"seq_region_name":"7","id":"rs1034369127","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140500755,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500755,"source":"dbSNP","seq_region_name":"7","id":"rs1795502038","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs977587481","end":140500757,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140500757,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs928783911","clinical_significance":[],"start":140500759,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140500759,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs765068575","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500761,"source":"dbSNP","strand":1,"feature_type":"variation","end":140500761,"alleles":["C","G","T"]},{"start":140500762,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140500762,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs958718510","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140500770,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140500770,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1479851275"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1177296310","end":140500772,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140500772,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140500773,"alleles":["-","AAGTG","AAGTGCTGAGC"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500774,"source":"dbSNP","seq_region_name":"7","id":"rs1795502302","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140500774,"alleles":["C","A","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500774,"clinical_significance":[],"seq_region_name":"7","id":"rs995493266"},{"source":"dbSNP","start":140500775,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140500774,"alleles":["-","TGAGCA"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795502374","seq_region_name":"7"},{"seq_region_name":"7","id":"rs567747515","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500777,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140500777},{"alleles":["G","A"],"end":140500778,"strand":1,"feature_type":"variation","start":140500778,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs184439570","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs372020935","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500785,"feature_type":"variation","strand":1,"alleles":["C","A","G","T"],"end":140500785},{"seq_region_name":"7","id":"rs1795502617","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500790,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140500790},{"clinical_significance":[],"seq_region_name":"7","id":"rs1158207412","source":"dbSNP","start":140500794,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140500794,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs547712264","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140500796,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500796},{"seq_region_name":"7","id":"rs772511060","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500799,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","-"],"end":140500799},{"clinical_significance":[],"seq_region_name":"7","id":"rs1352267045","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140500800,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500800},{"id":"rs1366022253","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140500809,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500809,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500810,"feature_type":"variation","strand":1,"end":140500810,"alleles":["G","A"],"clinical_significance":[],"id":"rs1237949388","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795502820","alleles":["A","G"],"end":140500817,"feature_type":"variation","strand":1,"source":"dbSNP","start":140500817,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795502838","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500822,"source":"dbSNP","strand":1,"feature_type":"variation","end":140500822,"alleles":["T","C"]},{"source":"dbSNP","start":140500824,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TTTTTTT","TTTTTT","TTTTTTTT"],"end":140500830,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs938948508"},{"end":140500825,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140500825,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130419773","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1402806110","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500828,"feature_type":"variation","strand":1,"end":140500828,"alleles":["T","G"]},{"feature_type":"variation","strand":1,"end":140500830,"alleles":["T","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500830,"clinical_significance":[],"seq_region_name":"7","id":"rs983358817"},{"seq_region_name":"7","id":"rs1795502952","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500831,"source":"dbSNP","strand":1,"feature_type":"variation","end":140500831,"alleles":["A","T"]},{"feature_type":"variation","strand":1,"end":140500835,"alleles":["G","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500835,"clinical_significance":[],"seq_region_name":"7","id":"rs1795502985"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795503007","feature_type":"variation","strand":1,"end":140500840,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500840},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585521621","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500843,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140500843},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500844,"source":"dbSNP","strand":1,"feature_type":"variation","end":140500846,"alleles":["TTT","TTTT"],"seq_region_name":"7","id":"rs1795503061","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140500847,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500847,"source":"dbSNP","seq_region_name":"7","id":"rs1318849407","clinical_significance":[]},{"id":"rs1795503111","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500848,"source":"dbSNP","strand":1,"feature_type":"variation","end":140500848,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs1585521625","clinical_significance":[],"end":140500849,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140500849,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140500851,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140500851,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795503168"},{"clinical_significance":[],"seq_region_name":"7","id":"rs375688992","source":"dbSNP","start":140500856,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140500856,"alleles":["G","A"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140500857,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500857,"clinical_significance":[],"seq_region_name":"7","id":"rs992136026"},{"end":140500858,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140500858,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795503258"},{"alleles":["A","T"],"end":140500860,"feature_type":"variation","strand":1,"source":"dbSNP","start":140500860,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1158056106"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500863,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140500863,"seq_region_name":"7","id":"rs916270016","clinical_significance":[]},{"source":"dbSNP","start":140500865,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140500865,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795503339"},{"start":140500869,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140500869,"strand":1,"feature_type":"variation","id":"rs571490080","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500870,"feature_type":"variation","strand":1,"end":140500870,"alleles":["C","G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs565734878"},{"clinical_significance":[],"seq_region_name":"7","id":"rs538974568","source":"dbSNP","start":140500871,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140500871,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795503430","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500874,"feature_type":"variation","strand":1,"end":140500874,"alleles":["C","A"]},{"id":"rs1795503456","seq_region_name":"7","clinical_significance":[],"start":140500875,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140500875,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"start":140500877,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140500877,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795503486","clinical_significance":[]},{"source":"dbSNP","start":140500881,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140500881,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795503512"},{"start":140500882,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140500882,"alleles":["C","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs539576027","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140500883,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500883,"source":"dbSNP","seq_region_name":"7","id":"rs1795503572","clinical_significance":[]},{"alleles":["C","A"],"end":140500886,"strand":1,"feature_type":"variation","start":140500886,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795503600","clinical_significance":[]},{"seq_region_name":"7","id":"rs1480291042","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140500889,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500889,"source":"dbSNP"},{"seq_region_name":"7","id":"rs912696751","clinical_significance":[],"end":140500890,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140500890,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1280247410","clinical_significance":[],"alleles":["T","C"],"end":140500891,"strand":1,"feature_type":"variation","start":140500891,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140500892,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500892,"source":"dbSNP","id":"rs1375539681","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140500894,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140500894,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795503751"},{"seq_region_name":"7","id":"rs1281603987","clinical_significance":[],"start":140500898,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140500898,"strand":1,"feature_type":"variation"},{"start":140500904,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140500904,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs966028271","clinical_significance":[]},{"start":140500909,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140500909,"strand":1,"feature_type":"variation","id":"rs1795503846","seq_region_name":"7","clinical_significance":[]},{"start":140500913,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140500913,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs975615198","clinical_significance":[]},{"end":140500914,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140500914,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1284746791","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1309155774","feature_type":"variation","strand":1,"end":140500948,"alleles":["TGAGCCACCACGCCCAGCGTGTGAGCCACC","TGAGCCACC"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500919},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500920,"feature_type":"variation","strand":1,"end":140500920,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1344686364"},{"feature_type":"variation","strand":1,"end":140500923,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500923,"clinical_significance":[],"id":"rs1795503951","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585521652","source":"dbSNP","start":140500928,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140500928,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140500929,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500929,"source":"dbSNP","seq_region_name":"7","id":"rs114348232","clinical_significance":[]},{"seq_region_name":"7","id":"rs1270531872","clinical_significance":[],"end":140500957,"alleles":["CGCCCAGCGTGTGAGCCACCGCGCCCAGC","CGCCCAGC"],"strand":1,"feature_type":"variation","start":140500929,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs936371864","seq_region_name":"7","source":"dbSNP","start":140500930,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140500930,"alleles":["G","A","T"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140500931,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500931,"clinical_significance":[],"id":"rs1053378811","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1317733276","clinical_significance":[],"end":140500936,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140500936,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs913641909","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500937,"feature_type":"variation","strand":1,"end":140500937,"alleles":["G","A"]},{"start":140500940,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140500940,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1289983689","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795504245","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500944,"feature_type":"variation","strand":1,"end":140500944,"alleles":["C","A","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500948,"source":"dbSNP","strand":1,"feature_type":"variation","end":140500948,"alleles":["C","T"],"seq_region_name":"7","id":"rs945110328","clinical_significance":[]},{"id":"rs11765322","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140500949,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500949,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1046670300","clinical_significance":[],"start":140500950,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140500950,"alleles":["C","A","T"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140500951,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140500951,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795504429"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1469462964","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500961,"feature_type":"variation","strand":1,"end":140500961,"alleles":["A","T"]},{"clinical_significance":[],"id":"rs1795504479","seq_region_name":"7","end":140500967,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140500967,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs906340696","seq_region_name":"7","alleles":["A","G"],"end":140500969,"feature_type":"variation","strand":1,"source":"dbSNP","start":140500969,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs2130419920","seq_region_name":"7","clinical_significance":[],"start":140500979,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140500979,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1795504531","seq_region_name":"7","feature_type":"variation","strand":1,"end":140500987,"alleles":["TTCCTTTC","TTC"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500980},{"end":140500981,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140500981,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs368304926"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140500982,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140500982,"clinical_significance":[],"id":"rs1002019632","seq_region_name":"7"},{"start":140500987,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","T"],"end":140500987,"strand":1,"feature_type":"variation","id":"rs1795504613","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1474714625","seq_region_name":"7","source":"dbSNP","start":140500988,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140500988,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1204692498","clinical_significance":[],"start":140500989,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140500989,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1241983366","clinical_significance":[],"strand":1,"feature_type":"variation","end":140500990,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140500990,"source":"dbSNP"},{"id":"rs1795504712","seq_region_name":"7","clinical_significance":[],"end":140500995,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140500995,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs867825009","seq_region_name":"7","clinical_significance":[],"alleles":["A","T"],"end":140500999,"strand":1,"feature_type":"variation","start":140500999,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs899719208","clinical_significance":[],"start":140501001,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G","T"],"end":140501001,"strand":1,"feature_type":"variation"},{"end":140501022,"alleles":["TTTATTTATTTATTTATTT","TTTATTTATTTATTT","TTTATTTATTTATTTATTTATTT"],"strand":1,"feature_type":"variation","start":140501004,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1479363247","clinical_significance":[]},{"source":"dbSNP","start":140501008,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TTT","TT"],"end":140501010,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795504823"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1201444494","feature_type":"variation","strand":1,"end":140501013,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501013},{"seq_region_name":"7","id":"rs1795504880","clinical_significance":[],"end":140501014,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140501014,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs537568247","clinical_significance":[],"end":140501018,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140501018,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795504917","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140501019,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501019,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1176613076","feature_type":"variation","strand":1,"alleles":["T","A","G"],"end":140501021,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501021},{"strand":1,"feature_type":"variation","end":140501023,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501023,"source":"dbSNP","id":"rs1011998318","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140501024,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501024,"clinical_significance":[],"seq_region_name":"7","id":"rs1795505011"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1446275155","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501028,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140501028},{"id":"rs1161472388","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501031,"source":"dbSNP","strand":1,"feature_type":"variation","end":140501031,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1697342452","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140501032,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501032},{"clinical_significance":[],"seq_region_name":"7","id":"rs547681595","feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140501038,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501038},{"seq_region_name":"7","id":"rs1453247149","clinical_significance":[],"start":140501039,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140501039,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"id":"rs762766260","seq_region_name":"7","clinical_significance":[],"start":140501044,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140501044,"strand":1,"feature_type":"variation"},{"start":140501044,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["GTTGCCCAGGCTGGAGTGCAGT","GTTGCCCAGGCTGGAGTGCAGTTGCCCAGGCTGGAGTGCAGT"],"end":140501065,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1404992718","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs995545771","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501053,"feature_type":"variation","strand":1,"end":140501053,"alleles":["G","A","C"]},{"seq_region_name":"7","id":"rs1795505222","clinical_significance":[],"end":140501054,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140501054,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs2130419996","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501063,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140501063},{"seq_region_name":"7","id":"rs1026949354","clinical_significance":[],"start":140501068,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140501068,"strand":1,"feature_type":"variation"},{"end":140501069,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140501069,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs951555092","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501072,"feature_type":"variation","strand":1,"end":140501072,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1452274024"},{"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140501078,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501078,"source":"dbSNP","id":"rs1355262950","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","A"],"end":140501086,"strand":1,"feature_type":"variation","start":140501086,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1004272047","clinical_significance":[]},{"seq_region_name":"7","id":"rs1408519804","clinical_significance":[],"end":140501091,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140501091,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1440109260","clinical_significance":[],"strand":1,"feature_type":"variation","end":140501093,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501093,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795505426","source":"dbSNP","start":140501099,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140501099,"alleles":["C","T"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501100,"feature_type":"variation","strand":1,"end":140501100,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795505451"},{"seq_region_name":"7","id":"rs1433153684","clinical_significance":[],"start":140501104,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140501104,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1020220382","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140501115,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501115,"source":"dbSNP"},{"id":"rs1331316481","seq_region_name":"7","clinical_significance":[],"start":140501118,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140501118,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1384211589","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501132,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140501132},{"id":"rs555252293","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501133,"source":"dbSNP","strand":1,"feature_type":"variation","end":140501133,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795505640","alleles":["G","A"],"end":140501135,"feature_type":"variation","strand":1,"source":"dbSNP","start":140501135,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501141,"feature_type":"variation","strand":1,"end":140501141,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795505667"},{"strand":1,"feature_type":"variation","end":140501145,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501145,"source":"dbSNP","seq_region_name":"7","id":"rs1585521728","clinical_significance":[]},{"source":"dbSNP","start":140501147,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140501147,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585521730"},{"clinical_significance":[],"seq_region_name":"7","id":"rs975541673","end":140501150,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140501150,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795505775","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501152,"source":"dbSNP","strand":1,"feature_type":"variation","end":140501152,"alleles":["A","G"]},{"feature_type":"variation","strand":1,"end":140501156,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501156,"clinical_significance":[],"id":"rs2130420044","seq_region_name":"7"},{"source":"dbSNP","start":140501157,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140501157,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs188971441","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795505841","clinical_significance":[],"start":140501158,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140501158,"strand":1,"feature_type":"variation"},{"start":140501159,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C","T"],"end":140501159,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1047300454","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs958282459","source":"dbSNP","start":140501163,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140501163,"alleles":["T","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1356015116","clinical_significance":[],"start":140501163,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140501163,"alleles":["T","-"],"strand":1,"feature_type":"variation"},{"alleles":["C","T"],"end":140501165,"feature_type":"variation","strand":1,"source":"dbSNP","start":140501165,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795505953"},{"start":140501166,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140501166,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795505982","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140501167,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501167,"source":"dbSNP","seq_region_name":"7","id":"rs1206390598","clinical_significance":[]},{"end":140501169,"alleles":["G","C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140501169,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130420073"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501171,"feature_type":"variation","strand":1,"end":140501171,"alleles":["A","C","G","T"],"clinical_significance":[],"id":"rs62484131","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs66667105","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501171,"feature_type":"variation","strand":1,"alleles":["AAA","A","AA"],"end":140501173},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563106627","feature_type":"variation","strand":1,"alleles":["-","T","TT","TTT","TTTTT","TTTTTT","TTTTTTT","TTTTTTTT","TTTTTTTTTT","TTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTT"],"end":140501172,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501173},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501173,"feature_type":"variation","strand":1,"end":140501173,"alleles":["A","C","G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs10435243"},{"source":"dbSNP","start":140501173,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AT","-"],"end":140501174,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs140835272"},{"seq_region_name":"7","id":"rs777782950","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501173,"source":"dbSNP","strand":1,"feature_type":"variation","end":140501174,"alleles":["AT","ATAT"]},{"source":"dbSNP","start":140501173,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140501175,"alleles":["ATT","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1463634077"},{"feature_type":"variation","strand":1,"end":140501176,"alleles":["ATTT","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501173,"clinical_significance":[],"seq_region_name":"7","id":"rs1563106629"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501173,"feature_type":"variation","strand":1,"end":140501177,"alleles":["ATTTT","-"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795506518"},{"seq_region_name":"7","id":"rs1313016918","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501173,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["ATTTTT","-"],"end":140501178},{"end":140501179,"alleles":["ATTTTTT","-"],"strand":1,"feature_type":"variation","start":140501173,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1245260297","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140501173,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140501180,"alleles":["ATTTTTTT","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1374353951","seq_region_name":"7"},{"start":140501173,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["ATTTTTTTT","-"],"end":140501181,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1300069128","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795506633","source":"dbSNP","start":140501173,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140501182,"alleles":["ATTTTTTTTT","-"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["ATTTTTTTTTT","-"],"end":140501183,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501173,"source":"dbSNP","seq_region_name":"7","id":"rs754194999","clinical_significance":[]},{"alleles":["ATTTTTTTTTTT","-"],"end":140501184,"feature_type":"variation","strand":1,"source":"dbSNP","start":140501173,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795506674"},{"id":"rs1795506696","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501174,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140501174},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501174,"feature_type":"variation","strand":1,"end":140501194,"alleles":["TTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTT","TTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTT"],"clinical_significance":[],"id":"rs1161151509","seq_region_name":"7"},{"alleles":["T","A"],"end":140501178,"feature_type":"variation","strand":1,"source":"dbSNP","start":140501178,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585521781"},{"clinical_significance":[],"id":"rs1795506908","seq_region_name":"7","alleles":["T","G"],"end":140501179,"feature_type":"variation","strand":1,"source":"dbSNP","start":140501179,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501181,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140501181,"id":"rs1243168602","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795506965","end":140501186,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140501186,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1585521791","clinical_significance":[],"start":140501191,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140501191,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1242317972","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501195,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140501195},{"end":140501196,"alleles":["GG","G"],"strand":1,"feature_type":"variation","start":140501195,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1181611023","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140501196,"alleles":["G","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501196,"clinical_significance":[],"seq_region_name":"7","id":"rs78902587"},{"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140501198,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501198,"source":"dbSNP","id":"rs1585521796","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501200,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140501200,"clinical_significance":[],"id":"rs1795507155","seq_region_name":"7"},{"alleles":["G","C"],"end":140501201,"strand":1,"feature_type":"variation","start":140501201,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1168781618","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795507213","source":"dbSNP","start":140501202,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140501202,"alleles":["A","G"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["AA","A"],"end":140501205,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501204,"source":"dbSNP","seq_region_name":"7","id":"rs1250886148","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130420216","alleles":["A","G"],"end":140501205,"feature_type":"variation","strand":1,"source":"dbSNP","start":140501205,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1222865294","alleles":["G","C"],"end":140501206,"feature_type":"variation","strand":1,"source":"dbSNP","start":140501206,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140501207,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501207,"source":"dbSNP","seq_region_name":"7","id":"rs1490823329","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs977494341","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140501209,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501209},{"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140501211,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501211,"clinical_significance":[],"seq_region_name":"7","id":"rs1035886812"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501212,"feature_type":"variation","strand":1,"end":140501212,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1421879718"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795507400","feature_type":"variation","strand":1,"end":140501214,"alleles":["TTT","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501212},{"seq_region_name":"7","id":"rs1795507425","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501215,"source":"dbSNP","strand":1,"feature_type":"variation","end":140501215,"alleles":["A","T"]},{"start":140501217,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140501217,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130420242","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140501224,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501224,"clinical_significance":[],"seq_region_name":"7","id":"rs1317633293"},{"seq_region_name":"7","id":"rs1795507475","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140501226,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501226,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1795507502","seq_region_name":"7","alleles":["T","C"],"end":140501231,"feature_type":"variation","strand":1,"source":"dbSNP","start":140501231,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501232,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","G"],"end":140501232,"seq_region_name":"7","id":"rs1795507527","clinical_significance":[]},{"end":140501236,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140501236,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs2130420274","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1408376124","clinical_significance":[],"alleles":["C","G"],"end":140501238,"strand":1,"feature_type":"variation","start":140501238,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140501238,"alleles":["C","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501238,"source":"dbSNP","seq_region_name":"7","id":"rs1795507588","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1309213888","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501239,"feature_type":"variation","strand":1,"alleles":["T","A","G"],"end":140501239},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501242,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140501242,"seq_region_name":"7","id":"rs1222344377","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140501244,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501244,"source":"dbSNP","seq_region_name":"7","id":"rs1372871233","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140501245,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501245,"source":"dbSNP","seq_region_name":"7","id":"rs1284334535","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501252,"source":"dbSNP","strand":1,"feature_type":"variation","end":140501252,"alleles":["T","G"],"seq_region_name":"7","id":"rs1795507717","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1407087775","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501255,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140501255},{"start":140501256,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140501256,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795507773","clinical_significance":[]},{"start":140501257,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140501257,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1364278295","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501259,"source":"dbSNP","strand":1,"feature_type":"variation","end":140501259,"alleles":["C","T"],"seq_region_name":"7","id":"rs1795507817","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501260,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140501260,"seq_region_name":"7","id":"rs1795507849","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501266,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140501266,"seq_region_name":"7","id":"rs2130420315","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs989557857","source":"dbSNP","start":140501270,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140501270,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501271,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140501271,"seq_region_name":"7","id":"rs913537412","clinical_significance":[]},{"end":140501275,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140501275,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs574121642","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501275,"source":"dbSNP","strand":1,"feature_type":"variation","end":140501277,"alleles":["AAA","A"],"seq_region_name":"7","id":"rs1345328040","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs991651493","feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140501276,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501276},{"seq_region_name":"7","id":"rs1795508043","clinical_significance":[],"start":140501278,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140501278,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"start":140501281,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140501281,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs945136706","clinical_significance":[]},{"alleles":["A","G"],"end":140501286,"strand":1,"feature_type":"variation","start":140501286,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1199905021","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130420358","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501290,"source":"dbSNP","strand":1,"feature_type":"variation","end":140501290,"alleles":["G","C"]},{"alleles":["C","A","T"],"end":140501300,"feature_type":"variation","strand":1,"source":"dbSNP","start":140501300,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795508096"},{"clinical_significance":[],"seq_region_name":"7","id":"rs149739010","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501301,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140501301},{"clinical_significance":[],"seq_region_name":"7","id":"rs927690475","feature_type":"variation","strand":1,"end":140501306,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501306},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501307,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140501307,"clinical_significance":[],"seq_region_name":"7","id":"rs974150487"},{"alleles":["C","A"],"end":140501309,"strand":1,"feature_type":"variation","start":140501309,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1486148317","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795508251","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501313,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140501313},{"alleles":["T","C"],"end":140501314,"feature_type":"variation","strand":1,"source":"dbSNP","start":140501314,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795508282"},{"id":"rs919592303","seq_region_name":"7","clinical_significance":[],"end":140501316,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140501316,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs766287137","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140501324,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501324,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501325,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140501325,"seq_region_name":"7","id":"rs1054961262","clinical_significance":[]},{"seq_region_name":"7","id":"rs1431888506","clinical_significance":[],"start":140501329,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140501329,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"end":140501331,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140501331,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1271623673","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130420393","clinical_significance":[],"start":140501332,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140501332,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1795508455","clinical_significance":[],"strand":1,"feature_type":"variation","end":140501343,"alleles":["AAAA","AAA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501340,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501346,"source":"dbSNP","strand":1,"feature_type":"variation","end":140501346,"alleles":["C","G"],"id":"rs4726847","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140501352,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AT","-"],"end":140501353,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795508533","seq_region_name":"7"},{"end":140501353,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140501353,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795508595","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140501354,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140501354,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs2130420414","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140501358,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501358,"clinical_significance":[],"seq_region_name":"7","id":"rs1795508637"},{"source":"dbSNP","start":140501361,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140501361,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795508660","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1585521871","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140501362,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501362,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795508732","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501363,"feature_type":"variation","strand":1,"end":140501363,"alleles":["A","G"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501365,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140501365,"clinical_significance":[],"seq_region_name":"7","id":"rs1263939384"},{"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140501370,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501370,"source":"dbSNP","seq_region_name":"7","id":"rs578194173","clinical_significance":[]},{"source":"dbSNP","start":140501371,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140501371,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1283025865"},{"source":"dbSNP","start":140501379,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140501379,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs2130420438","seq_region_name":"7"},{"clinical_significance":[],"id":"rs545548697","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140501381,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501381},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501382,"feature_type":"variation","strand":1,"end":140501382,"alleles":["C","T"],"clinical_significance":[],"id":"rs1795508897","seq_region_name":"7"},{"start":140501387,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140501387,"alleles":["A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs563753360","clinical_significance":[]},{"end":140501388,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140501388,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795508940","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795508955","end":140501389,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140501389,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["G","A"],"end":140501391,"strand":1,"feature_type":"variation","start":140501391,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795508979","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501399,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140501399,"clinical_significance":[],"seq_region_name":"7","id":"rs887092078"},{"feature_type":"variation","strand":1,"end":140501403,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501403,"clinical_significance":[],"id":"rs1795510138","seq_region_name":"7"},{"seq_region_name":"7","id":"rs533740120","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140501405,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501405,"source":"dbSNP"},{"source":"dbSNP","start":140501406,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140501406,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1450932955"},{"alleles":["G","-"],"end":140501406,"feature_type":"variation","strand":1,"source":"dbSNP","start":140501406,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795510233"},{"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140501407,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501407,"clinical_significance":[],"id":"rs541926300","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs531284258","alleles":["T","C","G"],"end":140501421,"feature_type":"variation","strand":1,"source":"dbSNP","start":140501421,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140501422,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140501422,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795510357"},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140501427,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501427,"source":"dbSNP","id":"rs1795510387","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501428,"feature_type":"variation","strand":1,"end":140501428,"alleles":["T","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs901259407"},{"alleles":["C","T"],"end":140501429,"feature_type":"variation","strand":1,"source":"dbSNP","start":140501429,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1447405627"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1195085709","source":"dbSNP","start":140501434,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140501434,"feature_type":"variation","strand":1},{"end":140501435,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140501435,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1429055738"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140501436,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501436,"clinical_significance":[],"seq_region_name":"7","id":"rs1795510548"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795510576","source":"dbSNP","start":140501439,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140501439,"alleles":["T","G"],"feature_type":"variation","strand":1},{"end":140501443,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140501443,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs997011937","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501444,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140501444,"seq_region_name":"7","id":"rs543149800","clinical_significance":[]},{"id":"rs1795510656","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140501446,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501446,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140501453,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501453,"source":"dbSNP","seq_region_name":"7","id":"rs1263694653","clinical_significance":[]},{"source":"dbSNP","start":140501456,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140501456,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1184881704"},{"seq_region_name":"7","id":"rs1795510732","clinical_significance":[],"start":140501457,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TGT","T"],"end":140501459,"strand":1,"feature_type":"variation"},{"end":140501458,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140501458,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1028411814","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795510786","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501464,"source":"dbSNP","strand":1,"feature_type":"variation","end":140501464,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1795510815","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140501467,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501467,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501468,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140501468,"seq_region_name":"7","id":"rs1474552043","clinical_significance":[]},{"end":140501472,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140501472,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs561339218","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501474,"source":"dbSNP","strand":1,"feature_type":"variation","end":140501474,"alleles":["T","C"],"seq_region_name":"7","id":"rs958293733","clinical_significance":[]},{"id":"rs754708498","seq_region_name":"7","clinical_significance":[],"start":140501484,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140501484,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140501489,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501489,"clinical_significance":[],"seq_region_name":"7","id":"rs1321665721"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501491,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140501491,"clinical_significance":[],"seq_region_name":"7","id":"rs1255774705"},{"id":"rs78405470","seq_region_name":"7","clinical_significance":[],"start":140501492,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140501492,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1021604997","alleles":["T","C"],"end":140501495,"feature_type":"variation","strand":1,"source":"dbSNP","start":140501495,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1043112103","source":"dbSNP","start":140501503,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140501503,"alleles":["G","A"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501504,"source":"dbSNP","strand":1,"feature_type":"variation","end":140501504,"alleles":["C","G"],"id":"rs2130420545","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","A"],"end":140501512,"feature_type":"variation","strand":1,"source":"dbSNP","start":140501512,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs966431430"},{"end":140501519,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140501519,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130420551","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501520,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140501520,"clinical_significance":[],"seq_region_name":"7","id":"rs982177433"},{"id":"rs1336800035","seq_region_name":"7","clinical_significance":[],"start":140501523,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140501523,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140501525,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140501525,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795511362"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1454311358","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501528,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140501528},{"seq_region_name":"7","id":"rs1403364091","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501529,"source":"dbSNP","strand":1,"feature_type":"variation","end":140501529,"alleles":["C","A","T"]},{"start":140501534,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140501534,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs752125721","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1470992102","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140501536,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501536},{"end":140501540,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140501540,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1174954270"},{"source":"dbSNP","start":140501540,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AGAAGAAGAAGA","AGAAGAAGA"],"end":140501551,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1171799741","seq_region_name":"7"},{"start":140501541,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140501541,"alleles":["G","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795511571","clinical_significance":[]},{"seq_region_name":"7","id":"rs541971684","clinical_significance":[],"start":140501542,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140501543,"alleles":["AA","A"],"strand":1,"feature_type":"variation"},{"alleles":["G","A"],"end":140501544,"strand":1,"feature_type":"variation","start":140501544,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795511629","clinical_significance":[]},{"seq_region_name":"7","id":"rs1374755480","clinical_significance":[],"start":140501546,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140501546,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs2130420580","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501546,"source":"dbSNP","strand":1,"feature_type":"variation","end":140501553,"alleles":["AGAAGAGA","AGA"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501558,"feature_type":"variation","strand":1,"end":140501558,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1168289247"},{"seq_region_name":"7","id":"rs1448772977","clinical_significance":[],"strand":1,"feature_type":"variation","end":140501559,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501559,"source":"dbSNP"},{"source":"dbSNP","start":140501561,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G","T"],"end":140501561,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1035792925"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795511731","alleles":["G","A"],"end":140501564,"feature_type":"variation","strand":1,"source":"dbSNP","start":140501564,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1185421099","seq_region_name":"7","clinical_significance":[],"alleles":["C","G","T"],"end":140501566,"strand":1,"feature_type":"variation","start":140501566,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501567,"source":"dbSNP","strand":1,"feature_type":"variation","end":140501567,"alleles":["A","T"],"seq_region_name":"7","id":"rs1795511787","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs927736803","source":"dbSNP","start":140501568,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140501568,"feature_type":"variation","strand":1},{"id":"rs1795511843","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501569,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140501569},{"strand":1,"feature_type":"variation","end":140501580,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501580,"source":"dbSNP","seq_region_name":"7","id":"rs1795511870","clinical_significance":[]},{"clinical_significance":[],"id":"rs1320731174","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140501582,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501582},{"end":140501583,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140501583,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795511927"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795511951","alleles":["A","G"],"end":140501584,"feature_type":"variation","strand":1,"source":"dbSNP","start":140501584,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["C","A","G"],"end":140501594,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501594,"clinical_significance":[],"id":"rs547084074","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs565928287","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140501597,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501597},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501606,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140501606,"seq_region_name":"7","id":"rs1795512032","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795512058","clinical_significance":[],"alleles":["G","A"],"end":140501608,"strand":1,"feature_type":"variation","start":140501608,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140501610,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140501610,"strand":1,"feature_type":"variation","id":"rs1795512089","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585521949","clinical_significance":[],"end":140501612,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140501612,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1196773411","alleles":["C","T"],"end":140501615,"feature_type":"variation","strand":1,"source":"dbSNP","start":140501615,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140501625,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501625,"clinical_significance":[],"seq_region_name":"7","id":"rs1795512150"},{"clinical_significance":[],"seq_region_name":"7","id":"rs937703790","feature_type":"variation","strand":1,"end":140501628,"alleles":["A","C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501628},{"end":140501629,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140501629,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795512202","clinical_significance":[]},{"start":140501632,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140501632,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130420638","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501634,"feature_type":"variation","strand":1,"end":140501634,"alleles":["G","A"],"clinical_significance":[],"id":"rs1249951549","seq_region_name":"7"},{"alleles":["G","A"],"end":140501643,"strand":1,"feature_type":"variation","start":140501643,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs960125448","clinical_significance":[]},{"source":"dbSNP","start":140501644,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140501644,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1283509532","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501649,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140501649,"id":"rs1585521955","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795512312","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501650,"source":"dbSNP","strand":1,"feature_type":"variation","end":140501650,"alleles":["C","A","G"]},{"id":"rs1795512351","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140501651,"alleles":["T","A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501651,"source":"dbSNP"},{"alleles":["G","A","C","T"],"end":140501653,"strand":1,"feature_type":"variation","start":140501653,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs4637729","clinical_significance":[]},{"id":"rs920398664","seq_region_name":"7","clinical_significance":[],"start":140501656,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140501656,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1795512629","clinical_significance":[],"end":140501657,"alleles":["T","C","G"],"strand":1,"feature_type":"variation","start":140501657,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501659,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140501659,"id":"rs73163274","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1338364385","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140501662,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501662},{"seq_region_name":"7","id":"rs1795512788","clinical_significance":[],"start":140501663,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140501663,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1795512841","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140501671,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501671,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501674,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140501674,"seq_region_name":"7","id":"rs1795512874","clinical_significance":[]},{"start":140501677,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140501677,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs778139877","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795512944","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501682,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140501682},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795512969","feature_type":"variation","strand":1,"end":140501687,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501687},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140501696,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501696,"source":"dbSNP","seq_region_name":"7","id":"rs1023096638","clinical_significance":[]},{"id":"rs1795513034","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140501698,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501698,"source":"dbSNP"},{"source":"dbSNP","start":140501703,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","AA"],"end":140501703,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795513057"},{"seq_region_name":"7","id":"rs1795513089","clinical_significance":[],"strand":1,"feature_type":"variation","end":140501704,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501704,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501708,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140501708,"seq_region_name":"7","id":"rs2130420707","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130420709","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140501712,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501712},{"seq_region_name":"7","id":"rs1398429333","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501713,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140501713},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140501714,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501714,"clinical_significance":[],"seq_region_name":"7","id":"rs1296229304"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1206753326","end":140501715,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140501715,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140501720,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140501720,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585521975"},{"seq_region_name":"7","id":"rs886345061","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140501723,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501723,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140501726,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501726,"source":"dbSNP","id":"rs1385722780","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501728,"feature_type":"variation","strand":1,"end":140501728,"alleles":["G","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs940073177"},{"clinical_significance":[],"seq_region_name":"7","id":"rs145657946","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140501733,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501733},{"feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140501738,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501738,"clinical_significance":[],"id":"rs1367929955","seq_region_name":"7"},{"clinical_significance":[],"id":"rs377178216","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501741,"feature_type":"variation","strand":1,"end":140501746,"alleles":["TTCTTT","TT"]},{"id":"rs1269828212","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501741,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TTCTTTT","TT"],"end":140501747},{"seq_region_name":"7","id":"rs901270686","clinical_significance":[],"strand":1,"feature_type":"variation","end":140501742,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501742,"source":"dbSNP"},{"source":"dbSNP","start":140501742,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TCT","T"],"end":140501744,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1182856377","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1421090816","feature_type":"variation","strand":1,"alleles":["C","-"],"end":140501743,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501743},{"source":"dbSNP","start":140501743,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140501743,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1490660896"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1481486584","source":"dbSNP","start":140501744,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140501744,"alleles":["T","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs57972172","source":"dbSNP","start":140501744,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTT","TTTTTTTTTTTT","TTTTTTTTTTTTT","TTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT"],"end":140501768,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795514001","alleles":["T","A","C"],"end":140501745,"feature_type":"variation","strand":1,"source":"dbSNP","start":140501745,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140501746,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501746,"clinical_significance":[],"id":"rs1196877997","seq_region_name":"7"},{"start":140501747,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140501747,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795514060","clinical_significance":[]},{"source":"dbSNP","start":140501748,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140501748,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1304918718"},{"alleles":["T","C"],"end":140501750,"feature_type":"variation","strand":1,"source":"dbSNP","start":140501750,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs964007285"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795514121","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140501751,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501751},{"seq_region_name":"7","id":"rs1795514148","clinical_significance":[],"start":140501756,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140501756,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140501760,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140501760,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795514170"},{"clinical_significance":[],"id":"rs1795514208","seq_region_name":"7","alleles":["T","C"],"end":140501762,"feature_type":"variation","strand":1,"source":"dbSNP","start":140501762,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1390179270","clinical_significance":[],"start":140501765,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140501765,"strand":1,"feature_type":"variation"},{"id":"rs1795514258","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501766,"source":"dbSNP","strand":1,"feature_type":"variation","end":140501769,"alleles":["TTTA","-"]},{"alleles":["TTA","-"],"end":140501769,"feature_type":"variation","strand":1,"source":"dbSNP","start":140501767,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795514280","seq_region_name":"7"},{"id":"rs1795514308","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140501768,"strand":1,"feature_type":"variation","start":140501768,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795514337","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["TA","-"],"end":140501769,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501768,"source":"dbSNP"},{"end":140501769,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140501769,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1256115816","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501771,"feature_type":"variation","strand":1,"alleles":["G","A","C","T"],"end":140501771,"clinical_significance":[],"id":"rs996856861","seq_region_name":"7"},{"alleles":["C","G","T"],"end":140501773,"strand":1,"feature_type":"variation","start":140501773,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1585522018","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501774,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140501774,"seq_region_name":"7","id":"rs1795514460","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795514483","clinical_significance":[],"start":140501777,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140501777,"strand":1,"feature_type":"variation"},{"id":"rs2130420833","seq_region_name":"7","clinical_significance":[],"alleles":["C","A"],"end":140501779,"strand":1,"feature_type":"variation","start":140501779,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140501783,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140501783,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795514515"},{"alleles":["C","T"],"end":140501789,"strand":1,"feature_type":"variation","start":140501789,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1159210692","clinical_significance":[]},{"alleles":["CCC","CC"],"end":140501793,"strand":1,"feature_type":"variation","start":140501791,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795514585","clinical_significance":[]},{"end":140501792,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140501792,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1028465565","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795514657","end":140501803,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140501803,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs893998096","source":"dbSNP","start":140501804,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140501804,"alleles":["G","A"],"feature_type":"variation","strand":1},{"start":140501807,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140501807,"strand":1,"feature_type":"variation","id":"rs879490398","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1011478258","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501808,"source":"dbSNP","strand":1,"feature_type":"variation","end":140501808,"alleles":["C","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501810,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140501810,"clinical_significance":[],"id":"rs1480947034","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795514839","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501811,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140501811},{"id":"rs1160743435","seq_region_name":"7","clinical_significance":[],"end":140501819,"alleles":["GC","GCGC"],"strand":1,"feature_type":"variation","start":140501818,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1197950908","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140501824,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501824,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140501825,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501825,"source":"dbSNP","id":"rs1795514934","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1021241373","clinical_significance":[],"start":140501826,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","G"],"end":140501826,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585522046","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501828,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140501828},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501829,"source":"dbSNP","strand":1,"feature_type":"variation","end":140501833,"alleles":["CCTCC","CCTCCTCC"],"id":"rs1451525844","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501833,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140501833,"clinical_significance":[],"seq_region_name":"7","id":"rs769774326"},{"clinical_significance":[],"id":"rs1205143944","seq_region_name":"7","alleles":["G","A"],"end":140501834,"feature_type":"variation","strand":1,"source":"dbSNP","start":140501834,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140501836,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140501836,"strand":1,"feature_type":"variation","id":"rs967360430","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795515142","source":"dbSNP","start":140501839,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140501839,"alleles":["C","T"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140501840,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501840,"source":"dbSNP","id":"rs1419478407","seq_region_name":"7","clinical_significance":[]},{"start":140501841,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140501841,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs537531988","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["GGG","GG"],"end":140501843,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501841,"source":"dbSNP","seq_region_name":"7","id":"rs1795515248","clinical_significance":[]},{"seq_region_name":"7","id":"rs1345962559","clinical_significance":[],"alleles":["G","A"],"end":140501842,"strand":1,"feature_type":"variation","start":140501842,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140501843,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140501843,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs981802179"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1034651786","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140501857,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501857},{"end":140501866,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140501866,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs555942877","clinical_significance":[]},{"seq_region_name":"7","id":"rs1402474978","clinical_significance":[],"start":140501867,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140501867,"strand":1,"feature_type":"variation"},{"start":140501868,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140501868,"alleles":["C","G"],"strand":1,"feature_type":"variation","id":"rs959125476","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140501870,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501870,"clinical_significance":[],"seq_region_name":"7","id":"rs749802008"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501872,"feature_type":"variation","strand":1,"end":140501872,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1322309220"},{"start":140501873,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140501873,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs990545922","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1470413315","source":"dbSNP","start":140501882,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140501882,"feature_type":"variation","strand":1},{"start":140501884,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140501884,"alleles":["A","G"],"strand":1,"feature_type":"variation","id":"rs1795515545","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501887,"feature_type":"variation","strand":1,"alleles":["ACAGGTGCCTACCACCAC","AC"],"end":140501904,"clinical_significance":[],"seq_region_name":"7","id":"rs2130420920"},{"clinical_significance":[],"seq_region_name":"7","id":"rs920324479","end":140501888,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140501888,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1277694446","source":"dbSNP","start":140501890,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140501890,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140501892,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501892,"clinical_significance":[],"seq_region_name":"7","id":"rs1477994989"},{"clinical_significance":[],"id":"rs148906624","seq_region_name":"7","source":"dbSNP","start":140501894,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140501894,"alleles":["C","A","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1448266289","clinical_significance":[],"start":140501895,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140501895,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140501896,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501896,"source":"dbSNP","seq_region_name":"7","id":"rs1245638956","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140501897,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501897,"source":"dbSNP","seq_region_name":"7","id":"rs1207776212","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795515852","seq_region_name":"7","alleles":["C","T"],"end":140501898,"feature_type":"variation","strand":1,"source":"dbSNP","start":140501898,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140501899,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140501899,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1323798305","seq_region_name":"7"},{"seq_region_name":"7","id":"rs2130420951","clinical_significance":[],"strand":1,"feature_type":"variation","end":140501903,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501903,"source":"dbSNP"},{"start":140501904,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140501904,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1264771215","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1217209071","source":"dbSNP","start":140501905,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140501905,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs912319179","seq_region_name":"7","end":140501906,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140501906,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140501908,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501908,"source":"dbSNP","seq_region_name":"7","id":"rs1293608604","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1490911589","source":"dbSNP","start":140501909,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140501909,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1563106770","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501911,"source":"dbSNP","strand":1,"feature_type":"variation","end":140501911,"alleles":["C","A"]},{"alleles":["A","C"],"end":140501913,"feature_type":"variation","strand":1,"source":"dbSNP","start":140501913,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1208221022"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795516130","feature_type":"variation","strand":1,"alleles":["TTTTT","TTTTTT"],"end":140501919,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501915},{"seq_region_name":"7","id":"rs1795516163","clinical_significance":[],"strand":1,"feature_type":"variation","end":140501916,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501916,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs181655754","alleles":["T","G"],"end":140501917,"feature_type":"variation","strand":1,"source":"dbSNP","start":140501917,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140501918,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501918,"clinical_significance":[],"seq_region_name":"7","id":"rs1795516229"},{"end":140501921,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140501921,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs943762670","seq_region_name":"7"},{"alleles":["-","G"],"end":140501925,"feature_type":"variation","strand":1,"source":"dbSNP","start":140501926,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1319956209","seq_region_name":"7"},{"alleles":["T","C"],"end":140501926,"strand":1,"feature_type":"variation","start":140501926,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1039981256","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs983685030","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501927,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140501927},{"alleles":["A","C","G"],"end":140501932,"strand":1,"feature_type":"variation","start":140501932,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs779274476","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795516428","clinical_significance":[],"end":140501935,"alleles":["T","C","G"],"strand":1,"feature_type":"variation","start":140501935,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1414222320","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501936,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140501936},{"source":"dbSNP","start":140501937,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140501937,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs553107564","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795516510","feature_type":"variation","strand":1,"end":140501939,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501939},{"id":"rs1420630099","seq_region_name":"7","clinical_significance":[],"start":140501941,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140501941,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140501944,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501944,"clinical_significance":[],"seq_region_name":"7","id":"rs944583564"},{"clinical_significance":[],"id":"rs1170197921","seq_region_name":"7","source":"dbSNP","start":140501945,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140501945,"alleles":["C","T"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140501946,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501946,"clinical_significance":[],"id":"rs1378972178","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140501947,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501947,"source":"dbSNP","id":"rs1795516639","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1448186583","clinical_significance":[],"start":140501949,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140501949,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["-","T"],"end":140501953,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501954,"clinical_significance":[],"seq_region_name":"7","id":"rs1387850923"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501955,"feature_type":"variation","strand":1,"end":140501955,"alleles":["C","A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1187307858"},{"seq_region_name":"7","id":"rs1795516741","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501958,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140501958},{"clinical_significance":[],"seq_region_name":"7","id":"rs1041035363","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501959,"feature_type":"variation","strand":1,"end":140501959,"alleles":["T","A","C"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501964,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140501964,"clinical_significance":[],"id":"rs901156155","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1795516838","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501970,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140501970},{"seq_region_name":"7","id":"rs1795516872","clinical_significance":[],"end":140501971,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140501971,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["C","T"],"end":140501972,"strand":1,"feature_type":"variation","start":140501972,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs185533717","clinical_significance":[]},{"end":140501977,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140501977,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1049827877"},{"seq_region_name":"7","id":"rs1387394478","clinical_significance":[],"end":140501980,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140501980,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1216317922","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501981,"feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140501981},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795517055","end":140501982,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140501982,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140501985,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140501985,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1422374058","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1246732840","clinical_significance":[],"start":140501989,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140501989,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140501990,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501990,"source":"dbSNP","seq_region_name":"7","id":"rs1385300954","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140501991,"source":"dbSNP","strand":1,"feature_type":"variation","end":140501991,"alleles":["C","T"],"id":"rs1301357125","seq_region_name":"7","clinical_significance":[]},{"end":140501992,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140501992,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs147668072"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1396670257","source":"dbSNP","start":140501993,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140501993,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs998872107","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140501997,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140501997},{"seq_region_name":"7","id":"rs1011111634","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502000,"source":"dbSNP","strand":1,"feature_type":"variation","end":140502000,"alleles":["A","G"]},{"start":140502007,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140502007,"alleles":["A","G"],"strand":1,"feature_type":"variation","id":"rs1042910887","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs557117830","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140502012,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502012},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130421059","alleles":["G","-"],"end":140502012,"feature_type":"variation","strand":1,"source":"dbSNP","start":140502012,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140502015,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140502015,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130421060"},{"end":140502016,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140502016,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795517412"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140502018,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502018,"source":"dbSNP","seq_region_name":"7","id":"rs1370421617","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140502019,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502019,"source":"dbSNP","seq_region_name":"7","id":"rs1326826552","clinical_significance":[]},{"end":140502020,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140502020,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1167444939"},{"alleles":["ACAGGCATGAGCCA","ACAGGCATGAGCCATGCACAGGCATGAGCCA"],"end":140502034,"feature_type":"variation","strand":1,"source":"dbSNP","start":140502021,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1376089903"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795517581","source":"dbSNP","start":140502023,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140502023,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140502024,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140502024,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795517616","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795517638","feature_type":"variation","strand":1,"alleles":["GG","G"],"end":140502025,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502024},{"alleles":["G","A"],"end":140502025,"strand":1,"feature_type":"variation","start":140502025,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1563106796","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502026,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140502026,"clinical_significance":[],"seq_region_name":"7","id":"rs1795517696"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1453240679","source":"dbSNP","start":140502029,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140502029,"alleles":["G","A"],"feature_type":"variation","strand":1},{"id":"rs1795517768","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140502034,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502034,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1795517793","seq_region_name":"7","end":140502035,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140502035,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140502036,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502036,"source":"dbSNP","seq_region_name":"7","id":"rs575474531","clinical_significance":[]},{"seq_region_name":"7","id":"rs1179809636","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502037,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140502037},{"clinical_significance":[],"seq_region_name":"7","id":"rs1472253465","end":140502045,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140502045,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs142388611","clinical_significance":[],"end":140502047,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140502047,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140502048,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502048,"source":"dbSNP","seq_region_name":"7","id":"rs1795518444","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795518480","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502051,"source":"dbSNP","strand":1,"feature_type":"variation","end":140502051,"alleles":["C","T"]},{"feature_type":"variation","strand":1,"end":140502052,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502052,"clinical_significance":[],"seq_region_name":"7","id":"rs1795518517"},{"alleles":["T","C"],"end":140502054,"feature_type":"variation","strand":1,"source":"dbSNP","start":140502054,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs564811780","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795518564","alleles":["A","G"],"end":140502057,"feature_type":"variation","strand":1,"source":"dbSNP","start":140502057,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1206949129","source":"dbSNP","start":140502060,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140502060,"alleles":["T","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs561402228","end":140502063,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140502063,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1273774356","seq_region_name":"7","source":"dbSNP","start":140502064,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140502064,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs959051900","seq_region_name":"7","end":140502068,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140502068,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140502070,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140502070,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795518714","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502077,"source":"dbSNP","strand":1,"feature_type":"variation","end":140502077,"alleles":["G","A"],"seq_region_name":"7","id":"rs963565655","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502078,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140502078,"clinical_significance":[],"id":"rs1361743247","seq_region_name":"7"},{"start":140502085,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140502085,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795518819","clinical_significance":[]},{"source":"dbSNP","start":140502100,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140502100,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs995073840"},{"end":140502102,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140502102,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1011907014"},{"alleles":["G","A"],"end":140502110,"strand":1,"feature_type":"variation","start":140502110,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795518911","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140502111,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502111,"clinical_significance":[],"seq_region_name":"7","id":"rs1027442204"},{"id":"rs951886087","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502116,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140502116},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795519044","source":"dbSNP","start":140502117,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140502117,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1026542587","clinical_significance":[],"strand":1,"feature_type":"variation","end":140502118,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502118,"source":"dbSNP"},{"alleles":["C","A","T"],"end":140502120,"strand":1,"feature_type":"variation","start":140502120,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs528966932","clinical_significance":[]},{"start":140502121,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140502122,"alleles":["TT","-"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795519156","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502126,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140502126,"clinical_significance":[],"seq_region_name":"7","id":"rs950934469"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795519191","source":"dbSNP","start":140502130,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140502130,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs540990522","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502131,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140502131},{"id":"rs2130421150","seq_region_name":"7","clinical_significance":[],"start":140502136,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140502142,"alleles":["ATGGGGA","ATGGGGAATGGGGA"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502139,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140502139,"seq_region_name":"7","id":"rs2130421151","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502143,"feature_type":"variation","strand":1,"end":140502143,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795519241"},{"strand":1,"feature_type":"variation","end":140502144,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502144,"source":"dbSNP","seq_region_name":"7","id":"rs1236382065","clinical_significance":[]},{"start":140502148,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","-"],"end":140502148,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1304325510","clinical_significance":[]},{"alleles":["G","T"],"end":140502151,"feature_type":"variation","strand":1,"source":"dbSNP","start":140502151,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1427090358","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1388639097","seq_region_name":"7","source":"dbSNP","start":140502154,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140502154,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502160,"feature_type":"variation","strand":1,"alleles":["GG","G"],"end":140502161,"clinical_significance":[],"id":"rs1162085960","seq_region_name":"7"},{"seq_region_name":"7","id":"rs982415608","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502161,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140502161},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140502162,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502162,"source":"dbSNP","seq_region_name":"7","id":"rs1408192434","clinical_significance":[]},{"source":"dbSNP","start":140502164,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140502164,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs983309315"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502168,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140502168,"seq_region_name":"7","id":"rs117577396","clinical_significance":[]},{"source":"dbSNP","start":140502173,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140502173,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1471509634"},{"seq_region_name":"7","id":"rs114380104","clinical_significance":[],"strand":1,"feature_type":"variation","end":140502175,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502175,"source":"dbSNP"},{"id":"rs975174850","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140502176,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502176,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1422428711","clinical_significance":[],"alleles":["T","C"],"end":140502178,"strand":1,"feature_type":"variation","start":140502178,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1489418473","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140502184,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502184},{"start":140502185,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140502185,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795519790","clinical_significance":[]},{"alleles":["C","T"],"end":140502186,"feature_type":"variation","strand":1,"source":"dbSNP","start":140502186,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795519823","seq_region_name":"7"},{"start":140502187,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140502187,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795519857","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130421197","clinical_significance":[],"end":140502193,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140502193,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1263759714","clinical_significance":[],"start":140502195,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140502195,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1220850022","seq_region_name":"7","source":"dbSNP","start":140502202,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140502202,"alleles":["G","A"],"feature_type":"variation","strand":1},{"start":140502205,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140502205,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795519949","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795519971","feature_type":"variation","strand":1,"end":140502208,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502208},{"source":"dbSNP","start":140502218,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140502218,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795520002"},{"source":"dbSNP","start":140502218,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140502220,"alleles":["CCC","CC"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1317765573"},{"seq_region_name":"7","id":"rs1795520062","clinical_significance":[],"start":140502219,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140502219,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1286562278","clinical_significance":[],"start":140502220,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140502240,"alleles":["CTGCAGCTGCCGGTTTTGCTG","CTG"],"strand":1,"feature_type":"variation"},{"start":140502221,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140502221,"alleles":["T","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795520114","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502229,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140502229,"seq_region_name":"7","id":"rs1563106836","clinical_significance":[]},{"seq_region_name":"7","id":"rs551425128","clinical_significance":[],"alleles":["C","T"],"end":140502230,"strand":1,"feature_type":"variation","start":140502230,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502231,"source":"dbSNP","strand":1,"feature_type":"variation","end":140502231,"alleles":["G","A"],"seq_region_name":"7","id":"rs1795520209","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140502233,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502233,"source":"dbSNP","seq_region_name":"7","id":"rs563468715","clinical_significance":[]},{"source":"dbSNP","start":140502246,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140502246,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585522281"},{"id":"rs1328968278","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140502247,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502247,"source":"dbSNP"},{"clinical_significance":[],"id":"rs2130421225","seq_region_name":"7","source":"dbSNP","start":140502249,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140502249,"feature_type":"variation","strand":1},{"end":140502252,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140502252,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1284316644"},{"start":140502257,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140502257,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs947257768","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502263,"feature_type":"variation","strand":1,"end":140502263,"alleles":["G","T"],"clinical_significance":[],"id":"rs1795520370","seq_region_name":"7"},{"alleles":["A","G"],"end":140502265,"strand":1,"feature_type":"variation","start":140502265,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795520405","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795520427","clinical_significance":[],"start":140502266,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140502266,"alleles":["T","C","G"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140502268,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502268,"clinical_significance":[],"seq_region_name":"7","id":"rs1407369796"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502269,"source":"dbSNP","strand":1,"feature_type":"variation","end":140502269,"alleles":["T","C"],"id":"rs1795520478","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs762056800","clinical_significance":[],"alleles":["A","C"],"end":140502274,"strand":1,"feature_type":"variation","start":140502274,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["G","T"],"end":140502275,"feature_type":"variation","strand":1,"source":"dbSNP","start":140502275,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1366025299"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795520556","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140502279,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502279},{"end":140502284,"alleles":["A","G","T"],"strand":1,"feature_type":"variation","start":140502284,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs921837077","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502285,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140502285,"seq_region_name":"7","id":"rs978560371","clinical_significance":[]},{"end":140502286,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140502286,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795520651"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1291302346","feature_type":"variation","strand":1,"end":140502287,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502287},{"clinical_significance":[],"seq_region_name":"7","id":"rs1435067439","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502289,"feature_type":"variation","strand":1,"alleles":["TTCTACACACAAGCTGTTCT","TTCT"],"end":140502308},{"strand":1,"feature_type":"variation","end":140502292,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502292,"source":"dbSNP","seq_region_name":"7","id":"rs530675583","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795520793","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140502293,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502293},{"start":140502294,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140502294,"strand":1,"feature_type":"variation","id":"rs1345234074","seq_region_name":"7","clinical_significance":[]},{"start":140502300,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140502300,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1160986157","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140502301,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502301,"source":"dbSNP","id":"rs1795520902","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","T"],"end":140502302,"strand":1,"feature_type":"variation","start":140502302,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1455305150","clinical_significance":[]},{"start":140502304,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140502304,"alleles":["G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1411045877","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140502306,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502306,"source":"dbSNP","seq_region_name":"7","id":"rs1163680199","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502309,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140502309,"clinical_significance":[],"seq_region_name":"7","id":"rs1176799773"},{"id":"rs35122631","seq_region_name":"7","clinical_significance":[],"end":140502314,"alleles":["AAAAA","AAAA","AAAAAA"],"strand":1,"feature_type":"variation","start":140502310,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795521065","source":"dbSNP","start":140502317,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140502317,"feature_type":"variation","strand":1},{"alleles":["A","G"],"end":140502318,"feature_type":"variation","strand":1,"source":"dbSNP","start":140502318,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1373263790"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502321,"source":"dbSNP","strand":1,"feature_type":"variation","end":140502321,"alleles":["A","G"],"seq_region_name":"7","id":"rs1795521122","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140502325,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502325,"source":"dbSNP","seq_region_name":"7","id":"rs924534134","clinical_significance":[]},{"seq_region_name":"7","id":"rs1463152579","clinical_significance":[],"alleles":["T","C"],"end":140502328,"strand":1,"feature_type":"variation","start":140502328,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1167952669","seq_region_name":"7","end":140502331,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140502331,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1190714953","seq_region_name":"7","alleles":["T","A"],"end":140502342,"feature_type":"variation","strand":1,"source":"dbSNP","start":140502342,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795521272","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502346,"feature_type":"variation","strand":1,"end":140502346,"alleles":["C","T"]},{"start":140502347,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140502347,"alleles":["A","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1486259617","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs549207439","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502349,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140502349},{"clinical_significance":[],"seq_region_name":"7","id":"rs1398840884","feature_type":"variation","strand":1,"alleles":["T","A"],"end":140502350,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502350},{"seq_region_name":"7","id":"rs1795521410","clinical_significance":[],"start":140502351,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140502351,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140502354,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140502354,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795521439","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1795521468","seq_region_name":"7","alleles":["C","A"],"end":140502356,"feature_type":"variation","strand":1,"source":"dbSNP","start":140502356,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795521498","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140502357,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502357},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502362,"feature_type":"variation","strand":1,"end":140502362,"alleles":["A","C"],"clinical_significance":[],"id":"rs1795521521","seq_region_name":"7"},{"start":140502363,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140502363,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1207129280","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140502364,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502364,"clinical_significance":[],"seq_region_name":"7","id":"rs115337963"},{"seq_region_name":"7","id":"rs545365985","clinical_significance":[],"strand":1,"feature_type":"variation","end":140502365,"alleles":["G","A","C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502365,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585522347","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502369,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140502369},{"id":"rs576417354","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502376,"source":"dbSNP","strand":1,"feature_type":"variation","end":140502376,"alleles":["C","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502377,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140502377,"clinical_significance":[],"seq_region_name":"7","id":"rs1301141557"},{"source":"dbSNP","start":140502378,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140502378,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795521770"},{"clinical_significance":[],"seq_region_name":"7","id":"rs895809991","end":140502382,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140502382,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1395206141","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502385,"source":"dbSNP","strand":1,"feature_type":"variation","end":140502385,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs146641175","alleles":["C","A","T"],"end":140502387,"feature_type":"variation","strand":1,"source":"dbSNP","start":140502387,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795521885","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502388,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140502388},{"clinical_significance":[],"id":"rs772445768","seq_region_name":"7","feature_type":"variation","strand":1,"end":140502398,"alleles":["TCTGTCTAT","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502390},{"seq_region_name":"7","id":"rs1387376914","clinical_significance":[],"alleles":["C","G"],"end":140502391,"strand":1,"feature_type":"variation","start":140502391,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs946756565","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502393,"source":"dbSNP","strand":1,"feature_type":"variation","end":140502393,"alleles":["G","A"]},{"source":"dbSNP","start":140502394,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140502394,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs768783505","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795522052","end":140502395,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140502395,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795522076","alleles":["T","C"],"end":140502396,"feature_type":"variation","strand":1,"source":"dbSNP","start":140502396,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1467350884","source":"dbSNP","start":140502400,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140502400,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795522115","end":140502404,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140502404,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502407,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140502407,"clinical_significance":[],"seq_region_name":"7","id":"rs1795522143"},{"alleles":["T","C"],"end":140502408,"strand":1,"feature_type":"variation","start":140502408,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1375692769","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795522196","clinical_significance":[],"start":140502410,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140502410,"alleles":["T","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1795522215","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502413,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140502413},{"clinical_significance":[],"seq_region_name":"7","id":"rs560356836","source":"dbSNP","start":140502426,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140502426,"alleles":["C","A","G"],"feature_type":"variation","strand":1},{"start":140502430,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140502430,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795522288","clinical_significance":[]},{"id":"rs1795522312","seq_region_name":"7","clinical_significance":[],"start":140502431,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140502431,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502435,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140502435,"seq_region_name":"7","id":"rs1795522335","clinical_significance":[]},{"seq_region_name":"7","id":"rs994980115","clinical_significance":[],"start":140502436,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140502436,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1585522384","clinical_significance":[],"alleles":["T","C"],"end":140502440,"strand":1,"feature_type":"variation","start":140502440,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795522414","feature_type":"variation","strand":1,"end":140502444,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502444},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502449,"feature_type":"variation","strand":1,"end":140502449,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1392178741"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1026401898","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502451,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140502451},{"clinical_significance":[],"id":"rs1795522494","seq_region_name":"7","feature_type":"variation","strand":1,"end":140502452,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502452},{"alleles":["C","-"],"end":140502453,"feature_type":"variation","strand":1,"source":"dbSNP","start":140502453,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1464626143","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1468580863","clinical_significance":[],"strand":1,"feature_type":"variation","end":140502453,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502453,"source":"dbSNP"},{"seq_region_name":"7","id":"rs886730120","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502454,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140502454},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795522610","alleles":["T","A"],"end":140502456,"feature_type":"variation","strand":1,"source":"dbSNP","start":140502456,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795522649","source":"dbSNP","start":140502460,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140502460,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502462,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140502462,"clinical_significance":[],"id":"rs1795522672","seq_region_name":"7"},{"start":140502464,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140502464,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs902656623","clinical_significance":[]},{"start":140502467,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140502467,"strand":1,"feature_type":"variation","id":"rs1795522738","seq_region_name":"7","clinical_significance":[]},{"id":"rs1795522764","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502469,"source":"dbSNP","strand":1,"feature_type":"variation","end":140502469,"alleles":["T","TT"]},{"seq_region_name":"7","id":"rs1003697796","clinical_significance":[],"end":140502473,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140502473,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795522811","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140502474,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502474,"source":"dbSNP"},{"alleles":["C","G"],"end":140502475,"feature_type":"variation","strand":1,"source":"dbSNP","start":140502475,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1482508745"},{"clinical_significance":[],"id":"rs1056764016","seq_region_name":"7","source":"dbSNP","start":140502477,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140502477,"alleles":["A","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1585522406","seq_region_name":"7","feature_type":"variation","strand":1,"end":140502479,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502479},{"start":140502480,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140502480,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795522927","clinical_significance":[]},{"id":"rs1205907040","seq_region_name":"7","clinical_significance":[],"alleles":["TTT","TTTTT"],"end":140502483,"strand":1,"feature_type":"variation","start":140502481,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140502485,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502485,"source":"dbSNP","seq_region_name":"7","id":"rs1795522989","clinical_significance":[]},{"seq_region_name":"7","id":"rs190402652","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502491,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140502491},{"seq_region_name":"7","id":"rs1795523079","clinical_significance":[],"strand":1,"feature_type":"variation","end":140502492,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502492,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1011960801","alleles":["G","A","C"],"end":140502494,"feature_type":"variation","strand":1,"source":"dbSNP","start":140502494,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1225482540","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140502498,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502498,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1027287683","source":"dbSNP","start":140502499,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140502499,"alleles":["G","T"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140502501,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502501,"source":"dbSNP","id":"rs1795523177","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1265505029","source":"dbSNP","start":140502503,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140502503,"alleles":["A","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs951839942","feature_type":"variation","strand":1,"end":140502505,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502505},{"clinical_significance":[],"seq_region_name":"7","id":"rs1313035598","source":"dbSNP","start":140502506,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140502506,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1482507381","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502511,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140502511},{"seq_region_name":"7","id":"rs1397397261","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502512,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140502512},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502514,"feature_type":"variation","strand":1,"end":140502514,"alleles":["C","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130421433"},{"seq_region_name":"7","id":"rs139221877","clinical_significance":[],"alleles":["G","A"],"end":140502517,"strand":1,"feature_type":"variation","start":140502517,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1014655208","seq_region_name":"7","source":"dbSNP","start":140502519,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140502519,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs966299715","clinical_significance":[],"alleles":["C","A","T"],"end":140502523,"strand":1,"feature_type":"variation","start":140502523,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs113826182","clinical_significance":[],"end":140502524,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140502524,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140502525,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140502525,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1462438845","seq_region_name":"7"},{"seq_region_name":"7","id":"rs562126478","clinical_significance":[],"end":140502527,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140502527,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1166822683","alleles":["A","T"],"end":140502530,"feature_type":"variation","strand":1,"source":"dbSNP","start":140502530,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs975458223","feature_type":"variation","strand":1,"end":140502531,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502531},{"strand":1,"feature_type":"variation","end":140502532,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502532,"source":"dbSNP","id":"rs1795523664","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs953256700","clinical_significance":[],"start":140502536,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140502536,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1422369477","seq_region_name":"7","end":140502538,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140502538,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140502540,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140502540,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1422274671","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502541,"source":"dbSNP","strand":1,"feature_type":"variation","end":140502540,"alleles":["-","G"],"seq_region_name":"7","id":"rs1189943991","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140502542,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502542,"source":"dbSNP","seq_region_name":"7","id":"rs1795523815","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1255905503","source":"dbSNP","start":140502543,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140502543,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs73163275","seq_region_name":"7","source":"dbSNP","start":140502546,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140502546,"alleles":["T","A","C"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140502547,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502547,"clinical_significance":[],"seq_region_name":"7","id":"rs1273058065"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795523959","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502549,"feature_type":"variation","strand":1,"end":140502549,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs968425051","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502554,"source":"dbSNP","strand":1,"feature_type":"variation","end":140502554,"alleles":["G","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502555,"feature_type":"variation","strand":1,"end":140502555,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795524019"},{"seq_region_name":"7","id":"rs1340907973","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502557,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140502557},{"start":140502560,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140502560,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs978596541","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795524105","clinical_significance":[],"start":140502561,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140502561,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs915198333","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140502563,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502563},{"id":"rs1795524139","seq_region_name":"7","clinical_significance":[],"start":140502564,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140502564,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795524160","end":140502568,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140502568,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502581,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140502581,"seq_region_name":"7","id":"rs1563106893","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502582,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140502582,"seq_region_name":"7","id":"rs1585522471","clinical_significance":[]},{"source":"dbSNP","start":140502582,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["CGGGCGGG","CGGG"],"end":140502589,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1563106894"},{"seq_region_name":"7","id":"rs557279284","clinical_significance":[],"start":140502583,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140502583,"alleles":["G","A","T"],"strand":1,"feature_type":"variation"},{"id":"rs2130421510","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140502585,"alleles":["GGG","GG"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502583,"source":"dbSNP"},{"seq_region_name":"7","id":"rs71173205","clinical_significance":[],"start":140502585,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["-","C"],"end":140502584,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs924439258","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502586,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140502586},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502587,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140502587,"seq_region_name":"7","id":"rs575537853","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502588,"feature_type":"variation","strand":1,"alleles":["G","C","T"],"end":140502588,"clinical_significance":[],"id":"rs1352296464","seq_region_name":"7"},{"end":140502589,"alleles":["G","A","C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140502589,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs924037763"},{"source":"dbSNP","start":140502590,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140502590,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1429009871"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502594,"source":"dbSNP","strand":1,"feature_type":"variation","end":140502594,"alleles":["C","G"],"seq_region_name":"7","id":"rs1585522481","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1366342459","end":140502596,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140502596,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1563106902","seq_region_name":"7","clinical_significance":[],"end":140502598,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140502598,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1165006343","source":"dbSNP","start":140502599,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140502599,"alleles":["G","A","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795524507","clinical_significance":[],"end":140502600,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140502600,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140502610,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140502610,"strand":1,"feature_type":"variation","id":"rs939534556","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1563106903","clinical_significance":[],"alleles":["A","G"],"end":140502611,"strand":1,"feature_type":"variation","start":140502611,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502612,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140502612,"seq_region_name":"7","id":"rs1795524557","clinical_significance":[]},{"end":140502614,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140502614,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1563106906","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1368065072","seq_region_name":"7","feature_type":"variation","strand":1,"end":140502615,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502615},{"clinical_significance":[],"seq_region_name":"7","id":"rs536409609","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502617,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140502617},{"id":"rs1183021085","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140502623,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502623,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795524645","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502624,"feature_type":"variation","strand":1,"end":140502624,"alleles":["G","A"]},{"clinical_significance":[],"id":"rs1473798667","seq_region_name":"7","end":140502626,"alleles":["T","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140502626,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795524677","source":"dbSNP","start":140502627,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140502627,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795524693","alleles":["G","A"],"end":140502629,"feature_type":"variation","strand":1,"source":"dbSNP","start":140502629,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1795524715","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502630,"feature_type":"variation","strand":1,"end":140502630,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795524730","end":140502631,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140502631,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140502632,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140502632,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs934600858","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs180889832","feature_type":"variation","strand":1,"end":140502633,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502633},{"feature_type":"variation","strand":1,"end":140502635,"alleles":["T","C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502635,"clinical_significance":[],"id":"rs1490655410","seq_region_name":"7"},{"clinical_significance":[],"id":"rs753396060","seq_region_name":"7","alleles":["G","A","T"],"end":140502637,"feature_type":"variation","strand":1,"source":"dbSNP","start":140502637,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1353851660","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502639,"source":"dbSNP","strand":1,"feature_type":"variation","end":140502639,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795524865","source":"dbSNP","start":140502641,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140502641,"alleles":["A","G"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502643,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140502643,"clinical_significance":[],"seq_region_name":"7","id":"rs1795524882"},{"alleles":["T","A"],"end":140502649,"feature_type":"variation","strand":1,"source":"dbSNP","start":140502649,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585522517"},{"end":140502650,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140502650,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585522525"},{"end":140502653,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140502653,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1056645030"},{"seq_region_name":"7","id":"rs1264455880","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502654,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140502654},{"start":140502656,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140502656,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130421611","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140502659,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502659,"clinical_significance":[],"seq_region_name":"7","id":"rs1228593662"},{"feature_type":"variation","strand":1,"end":140502662,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502662,"clinical_significance":[],"seq_region_name":"7","id":"rs1585522540"},{"seq_region_name":"7","id":"rs1795525005","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502663,"source":"dbSNP","strand":1,"feature_type":"variation","end":140502663,"alleles":["C","T"]},{"id":"rs1795525021","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140502664,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502664,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502667,"source":"dbSNP","strand":1,"feature_type":"variation","end":140502667,"alleles":["C","T"],"seq_region_name":"7","id":"rs1795525046","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502671,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140502671,"seq_region_name":"7","id":"rs1386792339","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795525111","seq_region_name":"7","source":"dbSNP","start":140502672,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140502672,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1286219340","feature_type":"variation","strand":1,"end":140502674,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502674},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502677,"source":"dbSNP","strand":1,"feature_type":"variation","end":140502677,"alleles":["A","G"],"seq_region_name":"7","id":"rs1795525172","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs917262851","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502680,"feature_type":"variation","strand":1,"end":140502680,"alleles":["G","A"]},{"feature_type":"variation","strand":1,"end":140502681,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502681,"clinical_significance":[],"seq_region_name":"7","id":"rs1276536254"},{"seq_region_name":"7","id":"rs1339991847","clinical_significance":[],"strand":1,"feature_type":"variation","end":140502682,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502682,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1585522556","seq_region_name":"7","feature_type":"variation","strand":1,"end":140502685,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502685},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502686,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140502686,"seq_region_name":"7","id":"rs1563106916","clinical_significance":[]},{"id":"rs948768232","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502689,"source":"dbSNP","strand":1,"feature_type":"variation","end":140502689,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs866899634","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140502690,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502690,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1160243247","clinical_significance":[],"strand":1,"feature_type":"variation","end":140502695,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502695,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795525412","clinical_significance":[],"alleles":["A","G"],"end":140502696,"strand":1,"feature_type":"variation","start":140502696,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1459010907","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502704,"feature_type":"variation","strand":1,"end":140502704,"alleles":["T","C"]},{"id":"rs150460616","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140502705,"strand":1,"feature_type":"variation","start":140502705,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140502706,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140502706,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1158805333","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1481058203","feature_type":"variation","strand":1,"end":140502716,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502716},{"clinical_significance":[],"id":"rs948254136","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502717,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140502717},{"end":140502718,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140502718,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs540800855","clinical_significance":[]},{"id":"rs1449420162","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140502721,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502721,"source":"dbSNP"},{"source":"dbSNP","start":140502722,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140502722,"alleles":["C","A","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1487048108"},{"clinical_significance":[],"id":"rs559289125","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502723,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140502723},{"feature_type":"variation","strand":1,"end":140502725,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502725,"clinical_significance":[],"seq_region_name":"7","id":"rs113770060"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502728,"feature_type":"variation","strand":1,"end":140502728,"alleles":["G","GTG"],"clinical_significance":[],"seq_region_name":"7","id":"rs879402201"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140502729,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502729,"clinical_significance":[],"seq_region_name":"7","id":"rs759309292"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502730,"feature_type":"variation","strand":1,"end":140502729,"alleles":["-","GG"],"clinical_significance":[],"id":"rs1209037062","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2363813","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502730,"feature_type":"variation","strand":1,"end":140502730,"alleles":["A","C","G","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502730,"source":"dbSNP","strand":1,"feature_type":"variation","end":140502731,"alleles":["AA","GG"],"seq_region_name":"7","id":"rs71531983","clinical_significance":[]},{"end":140502731,"alleles":["AA","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140502730,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs759627971"},{"end":140502731,"alleles":["AA","A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140502730,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1554454391"},{"id":"rs386718475","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["AAGCA","GCGTG"],"end":140502734,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502730,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795526150","alleles":["-","GG"],"end":140502730,"feature_type":"variation","strand":1,"source":"dbSNP","start":140502731,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["A","C","G","T"],"end":140502731,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502731,"source":"dbSNP","seq_region_name":"7","id":"rs2363814","clinical_significance":[]},{"source":"dbSNP","start":140502731,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AG","-"],"end":140502732,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1345669983"},{"seq_region_name":"7","id":"rs777563008","clinical_significance":[],"end":140502732,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140502732,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140502733,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140502733,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs199561885","clinical_significance":[]},{"id":"rs1491474764","seq_region_name":"7","clinical_significance":[],"end":140502735,"alleles":["CAC","C"],"strand":1,"feature_type":"variation","start":140502733,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs775757141","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502734,"feature_type":"variation","strand":1,"alleles":["-","GT"],"end":140502733},{"clinical_significance":[],"seq_region_name":"7","id":"rs200729050","source":"dbSNP","start":140502734,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G","T"],"end":140502734,"feature_type":"variation","strand":1},{"id":"rs1563106938","seq_region_name":"7","clinical_significance":[],"end":140502734,"alleles":["-","GG","TG"],"strand":1,"feature_type":"variation","start":140502735,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1795526595","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140502735,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502735},{"seq_region_name":"7","id":"rs1432530649","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502736,"source":"dbSNP","strand":1,"feature_type":"variation","end":140502736,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1427666433","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502738,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140502738},{"clinical_significance":[],"seq_region_name":"7","id":"rs1015119764","alleles":["A","C"],"end":140502740,"feature_type":"variation","strand":1,"source":"dbSNP","start":140502740,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140502741,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140502741,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs549170751"},{"feature_type":"variation","strand":1,"end":140502744,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502744,"clinical_significance":[],"id":"rs1585522621","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502745,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140502745,"clinical_significance":[],"seq_region_name":"7","id":"rs1376577570"},{"strand":1,"feature_type":"variation","end":140502748,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502748,"source":"dbSNP","seq_region_name":"7","id":"rs1795526702","clinical_significance":[]},{"id":"rs1188575341","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140502749,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502749,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502753,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140502753,"clinical_significance":[],"seq_region_name":"7","id":"rs901589002"},{"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140502754,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502754,"source":"dbSNP","id":"rs1563106946","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795526786","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502754,"feature_type":"variation","strand":1,"alleles":["GGGCAGGG","GGG"],"end":140502761},{"strand":1,"feature_type":"variation","end":140502756,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502756,"source":"dbSNP","seq_region_name":"7","id":"rs1795526807","clinical_significance":[]},{"id":"rs1296631766","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140502757,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502757,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795526849","clinical_significance":[],"start":140502757,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","-"],"end":140502757,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1795526869","seq_region_name":"7","source":"dbSNP","start":140502759,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140502764,"alleles":["GGGGGG","GG"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140502760,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140502760,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs997305412"},{"end":140502762,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140502762,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1019210763","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140502763,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502763,"source":"dbSNP","seq_region_name":"7","id":"rs900720983","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795526979","clinical_significance":[],"end":140502765,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140502765,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502765,"feature_type":"variation","strand":1,"alleles":["CC","C"],"end":140502766,"clinical_significance":[],"seq_region_name":"7","id":"rs1795527003"},{"seq_region_name":"7","id":"rs1405734542","clinical_significance":[],"alleles":["C","T"],"end":140502766,"strand":1,"feature_type":"variation","start":140502766,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs10253841","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502767,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140502767},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795527127","source":"dbSNP","start":140502771,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140502771,"alleles":["C","T"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140502772,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140502772,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795527157"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502775,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140502775,"seq_region_name":"7","id":"rs1298442363","clinical_significance":[]},{"alleles":["G","A"],"end":140502776,"strand":1,"feature_type":"variation","start":140502776,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1230639554","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs12538900","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140502778,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502778},{"seq_region_name":"7","id":"rs1219219020","clinical_significance":[],"strand":1,"feature_type":"variation","end":140502779,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502779,"source":"dbSNP"},{"seq_region_name":"7","id":"rs968497714","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502780,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140502780},{"start":140502781,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140502781,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs990002861","clinical_significance":[]},{"id":"rs1795527439","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502783,"source":"dbSNP","strand":1,"feature_type":"variation","end":140502783,"alleles":["T","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1332526877","source":"dbSNP","start":140502784,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140502784,"feature_type":"variation","strand":1},{"id":"rs1414410390","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140502785,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502785,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs867716946","end":140502786,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140502786,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1585522657","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140502787,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502787,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs968483068","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502788,"feature_type":"variation","strand":1,"end":140502788,"alleles":["C","T"]},{"source":"dbSNP","start":140502790,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140502790,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1450835943"},{"clinical_significance":[],"seq_region_name":"7","id":"rs978110792","source":"dbSNP","start":140502791,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140502791,"feature_type":"variation","strand":1},{"end":140502796,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140502796,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795527647"},{"strand":1,"feature_type":"variation","end":140502797,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502797,"source":"dbSNP","seq_region_name":"7","id":"rs57993427","clinical_significance":[]},{"alleles":["G","A"],"end":140502798,"feature_type":"variation","strand":1,"source":"dbSNP","start":140502798,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs939379042"},{"clinical_significance":[],"id":"rs1795527767","seq_region_name":"7","end":140502799,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140502799,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs142457023","feature_type":"variation","strand":1,"end":140502801,"alleles":["A","C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502801},{"strand":1,"feature_type":"variation","end":140502802,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502802,"source":"dbSNP","seq_region_name":"7","id":"rs145976927","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140502804,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502804,"source":"dbSNP","seq_region_name":"7","id":"rs1244532184","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs56913990","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502809,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140502809},{"clinical_significance":[],"seq_region_name":"7","id":"rs1273997789","source":"dbSNP","start":140502810,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140502810,"alleles":["G","A","C","T"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140502812,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502812,"clinical_significance":[],"seq_region_name":"7","id":"rs1795528016"},{"seq_region_name":"7","id":"rs1585522682","clinical_significance":[],"strand":1,"feature_type":"variation","end":140502814,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502814,"source":"dbSNP"},{"clinical_significance":[],"id":"rs569175904","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140502815,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502815},{"seq_region_name":"7","id":"rs1795528111","clinical_significance":[],"start":140502818,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140502818,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502821,"source":"dbSNP","strand":1,"feature_type":"variation","end":140502821,"alleles":["A","G","T"],"seq_region_name":"7","id":"rs148659666","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502822,"source":"dbSNP","strand":1,"feature_type":"variation","end":140502822,"alleles":["C","G","T"],"seq_region_name":"7","id":"rs554725460","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502823,"source":"dbSNP","strand":1,"feature_type":"variation","end":140502823,"alleles":["G","A"],"seq_region_name":"7","id":"rs940387942","clinical_significance":[]},{"clinical_significance":[],"id":"rs1437694257","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502824,"feature_type":"variation","strand":1,"end":140502824,"alleles":["C","T"]},{"strand":1,"feature_type":"variation","end":140502828,"alleles":["C","A","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502828,"source":"dbSNP","seq_region_name":"7","id":"rs573396118","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs901607767","source":"dbSNP","start":140502829,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140502829,"feature_type":"variation","strand":1},{"alleles":["C","T"],"end":140502830,"strand":1,"feature_type":"variation","start":140502830,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795528349","clinical_significance":[]},{"start":140502832,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140502832,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs997193787","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502837,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140502837,"seq_region_name":"7","id":"rs1585522695","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs186116848","source":"dbSNP","start":140502840,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140502840,"feature_type":"variation","strand":1},{"alleles":["G","A"],"end":140502841,"strand":1,"feature_type":"variation","start":140502841,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1028801128","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1415449774","feature_type":"variation","strand":1,"end":140502845,"alleles":["GGGGG","GGG","GGGGGG"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502841},{"end":140502845,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140502845,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795528512","clinical_significance":[]},{"source":"dbSNP","start":140502847,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140502847,"alleles":["C","A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs757179355"},{"id":"rs1795528587","seq_region_name":"7","clinical_significance":[],"start":140502852,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140502852,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140502853,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140502853,"alleles":["T","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585522707"},{"start":140502856,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140502856,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795528622","clinical_significance":[]},{"seq_region_name":"7","id":"rs1252252583","clinical_significance":[],"end":140502857,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140502857,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140502861,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140502861,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795528651","clinical_significance":[]},{"end":140502864,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140502864,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795528662"},{"id":"rs1167161724","seq_region_name":"7","clinical_significance":[],"start":140502865,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140502865,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795528710","feature_type":"variation","strand":1,"end":140502865,"alleles":["-","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502866},{"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140502866,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502866,"source":"dbSNP","seq_region_name":"7","id":"rs1184334391","clinical_significance":[]},{"clinical_significance":[],"id":"rs1348281097","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140502867,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502867},{"seq_region_name":"7","id":"rs574488951","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["AAAAAAAAAAAAAAA","AAAAAAAAAAAA","AAAAAAAAAAAAA","AAAAAAAAAAAAAA","AAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAA"],"end":140502881,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502867,"source":"dbSNP"},{"seq_region_name":"7","id":"rs888972710","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502871,"source":"dbSNP","strand":1,"feature_type":"variation","end":140502871,"alleles":["A","C"]},{"end":140502880,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140502880,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1011396062","clinical_significance":[]},{"alleles":["-","C"],"end":140502880,"feature_type":"variation","strand":1,"source":"dbSNP","start":140502881,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1299292894"},{"seq_region_name":"7","id":"rs1795528917","clinical_significance":[],"start":140502881,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140502881,"strand":1,"feature_type":"variation"},{"alleles":["T","A"],"end":140502882,"feature_type":"variation","strand":1,"source":"dbSNP","start":140502882,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1379797418"},{"source":"dbSNP","start":140502886,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140502886,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1288037142"},{"clinical_significance":[],"seq_region_name":"7","id":"rs552745468","alleles":["C","T"],"end":140502887,"feature_type":"variation","strand":1,"source":"dbSNP","start":140502887,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140502890,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502890,"source":"dbSNP","seq_region_name":"7","id":"rs1585522747","clinical_significance":[]},{"seq_region_name":"7","id":"rs1330317127","clinical_significance":[],"start":140502894,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140502894,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs944048310","source":"dbSNP","start":140502895,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140502895,"alleles":["T","C","G"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140502898,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502898,"clinical_significance":[],"id":"rs780163149","seq_region_name":"7"},{"seq_region_name":"7","id":"rs978502163","clinical_significance":[],"start":140502899,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140502899,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs944886604","clinical_significance":[],"start":140502900,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140502900,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502906,"feature_type":"variation","strand":1,"end":140502906,"alleles":["T","C"],"clinical_significance":[],"id":"rs1795529231","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502908,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140502908,"seq_region_name":"7","id":"rs577676153","clinical_significance":[]},{"end":140502908,"alleles":["T","TT"],"strand":1,"feature_type":"variation","start":140502908,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795529280","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140502909,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502909,"source":"dbSNP","seq_region_name":"7","id":"rs1795529302","clinical_significance":[]},{"id":"rs1795529322","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502910,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140502910},{"seq_region_name":"7","id":"rs1287262421","clinical_significance":[],"end":140502915,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140502915,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1795529360","seq_region_name":"7","source":"dbSNP","start":140502916,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140502916,"alleles":["G","A"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502919,"source":"dbSNP","strand":1,"feature_type":"variation","end":140502919,"alleles":["A","G"],"seq_region_name":"7","id":"rs1320640095","clinical_significance":[]},{"alleles":["T","C"],"end":140502922,"feature_type":"variation","strand":1,"source":"dbSNP","start":140502922,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1321236012"},{"feature_type":"variation","strand":1,"end":140502923,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502923,"clinical_significance":[],"id":"rs755513182","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1412525566","alleles":["G","A"],"end":140502927,"feature_type":"variation","strand":1,"source":"dbSNP","start":140502927,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140502929,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502929,"source":"dbSNP","seq_region_name":"7","id":"rs992222653","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585522790","source":"dbSNP","start":140502931,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140502931,"alleles":["G","A"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502934,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140502934,"clinical_significance":[],"seq_region_name":"7","id":"rs1795529486"},{"end":140502936,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140502936,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1049441932","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795529528","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502937,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140502937},{"source":"dbSNP","start":140502938,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140502938,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs916652100","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1585522794","clinical_significance":[],"end":140502941,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140502941,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795529583","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502943,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140502943},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502946,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140502946,"id":"rs1795529600","seq_region_name":"7","clinical_significance":[]},{"id":"rs142147052","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502947,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140502947},{"id":"rs984973359","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140502949,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502949,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140502954,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502954,"source":"dbSNP","seq_region_name":"7","id":"rs1456390231","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502957,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140502957,"clinical_significance":[],"seq_region_name":"7","id":"rs1795529698"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140502959,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502959,"clinical_significance":[],"seq_region_name":"7","id":"rs999970469"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1489532383","end":140502961,"alleles":["T","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140502961,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs370323562","clinical_significance":[],"start":140502963,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140502963,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs2130421971","clinical_significance":[],"alleles":["C","T"],"end":140502965,"strand":1,"feature_type":"variation","start":140502965,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795529816","alleles":["G","A"],"end":140502970,"feature_type":"variation","strand":1,"source":"dbSNP","start":140502970,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","T"],"end":140502977,"feature_type":"variation","strand":1,"source":"dbSNP","start":140502977,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1245041535"},{"alleles":["G","A"],"end":140502981,"strand":1,"feature_type":"variation","start":140502981,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585522807","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502983,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140502983,"id":"rs1795529870","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502984,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","G"],"end":140502984,"seq_region_name":"7","id":"rs955746547","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140502986,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502986,"source":"dbSNP","id":"rs563294535","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140502988,"feature_type":"variation","strand":1,"end":140502988,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1014096508"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795530010","source":"dbSNP","start":140502989,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140502989,"alleles":["C","T"],"feature_type":"variation","strand":1},{"end":140502995,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140502995,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1226893253"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140502996,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140502996,"source":"dbSNP","seq_region_name":"7","id":"rs1177865902","clinical_significance":[]},{"source":"dbSNP","start":140502998,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140502998,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1302637016","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1243592174","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503001,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140503001},{"clinical_significance":[],"seq_region_name":"7","id":"rs909455431","source":"dbSNP","start":140503003,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140503003,"alleles":["C","A","G","T"],"feature_type":"variation","strand":1},{"start":140503004,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140503004,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs575587873","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795530134","seq_region_name":"7","feature_type":"variation","strand":1,"end":140503006,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503006},{"start":140503010,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140503010,"strand":1,"feature_type":"variation","id":"rs1585522840","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","G"],"end":140503011,"strand":1,"feature_type":"variation","start":140503011,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs533569529","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130422019","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140503016,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503016},{"id":"rs1795530191","seq_region_name":"7","clinical_significance":[],"start":140503020,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140503020,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["T","-"],"end":140503023,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503023,"source":"dbSNP","seq_region_name":"7","id":"rs1795530212","clinical_significance":[]},{"end":140503024,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140503024,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795530235"},{"start":140503025,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AAAATAAAATAA","AAAATAA"],"end":140503036,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1411870710","clinical_significance":[]},{"source":"dbSNP","start":140503033,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["ATAAGA","A"],"end":140503038,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795530277"},{"seq_region_name":"7","id":"rs970033957","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140503037,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503037,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["AAAAA","AAAAAA"],"end":140503042,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503038,"source":"dbSNP","id":"rs1344358541","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795530332","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503040,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140503040},{"seq_region_name":"7","id":"rs1176777095","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503042,"source":"dbSNP","strand":1,"feature_type":"variation","end":140503042,"alleles":["A","G"]},{"source":"dbSNP","start":140503047,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140503047,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795530364"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795530377","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503050,"feature_type":"variation","strand":1,"end":140503050,"alleles":["A","C"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503054,"source":"dbSNP","strand":1,"feature_type":"variation","end":140503054,"alleles":["A","T"],"seq_region_name":"7","id":"rs190046616","clinical_significance":[]},{"alleles":["A","G"],"end":140503057,"strand":1,"feature_type":"variation","start":140503057,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795530408","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140503058,"alleles":["G","C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503058,"clinical_significance":[],"seq_region_name":"7","id":"rs10435202"},{"source":"dbSNP","start":140503059,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140503059,"alleles":["A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1193023016"},{"source":"dbSNP","start":140503060,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140503060,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1450350457"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795530536","end":140503063,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140503063,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795530561","end":140503069,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140503069,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140503073,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140503073,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795530585","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503075,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140503075,"clinical_significance":[],"seq_region_name":"7","id":"rs1250092480"},{"clinical_significance":[],"id":"rs922916985","seq_region_name":"7","alleles":["G","A"],"end":140503078,"feature_type":"variation","strand":1,"source":"dbSNP","start":140503078,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795530644","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140503088,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503088,"source":"dbSNP"},{"start":140503090,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C","G"],"end":140503090,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs952063780","clinical_significance":[]},{"source":"dbSNP","start":140503091,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140503091,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1256945888","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140503095,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503095,"source":"dbSNP","seq_region_name":"7","id":"rs1795530705","clinical_significance":[]},{"seq_region_name":"7","id":"rs1171265541","clinical_significance":[],"end":140503099,"alleles":["G","C","T"],"strand":1,"feature_type":"variation","start":140503099,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1795530748","seq_region_name":"7","feature_type":"variation","strand":1,"end":140503103,"alleles":["GGGGG","GG"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503099},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503101,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140503101,"clinical_significance":[],"seq_region_name":"7","id":"rs1402472224"},{"strand":1,"feature_type":"variation","end":140503102,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503102,"source":"dbSNP","id":"rs1795530812","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1310892085","source":"dbSNP","start":140503105,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140503105,"alleles":["A","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1300646524","clinical_significance":[],"start":140503107,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140503111,"alleles":["GGGGG","GGGG","GGGGGG"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1464534693","clinical_significance":[],"alleles":["G","A"],"end":140503109,"strand":1,"feature_type":"variation","start":140503109,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795530939","end":140503111,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140503111,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795531013","clinical_significance":[],"start":140503113,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140503113,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs932970690","clinical_significance":[],"strand":1,"feature_type":"variation","end":140503114,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503114,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140503116,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503116,"clinical_significance":[],"seq_region_name":"7","id":"rs1795531081"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503123,"feature_type":"variation","strand":1,"end":140503123,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795531108"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140503125,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503125,"clinical_significance":[],"id":"rs1331251613","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503133,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140503133,"clinical_significance":[],"id":"rs754296397","seq_region_name":"7"},{"end":140503134,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140503134,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs888858138"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503140,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140503140,"seq_region_name":"7","id":"rs1795531233","clinical_significance":[]},{"alleles":["T","C"],"end":140503141,"feature_type":"variation","strand":1,"source":"dbSNP","start":140503141,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1361095119"},{"start":140503142,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140503142,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130422127","clinical_significance":[]},{"seq_region_name":"7","id":"rs907971055","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["AAAAAAAA","AAAAA","AAAAAAA","AAAAAAAAA"],"end":140503149,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503142,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503144,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140503144,"clinical_significance":[],"id":"rs1378029631","seq_region_name":"7"},{"seq_region_name":"7","id":"rs183167175","clinical_significance":[],"start":140503146,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140503146,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140503149,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503149,"clinical_significance":[],"seq_region_name":"7","id":"rs1430529861"},{"start":140503152,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140503152,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1392078026","clinical_significance":[]},{"clinical_significance":[],"id":"rs1259442579","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140503156,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503156},{"start":140503157,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140503157,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795531492","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585522911","clinical_significance":[],"start":140503158,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140503158,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140503167,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140503167,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1186976340"},{"feature_type":"variation","strand":1,"end":140503168,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503168,"clinical_significance":[],"seq_region_name":"7","id":"rs1795531549"},{"alleles":["A","G"],"end":140503171,"strand":1,"feature_type":"variation","start":140503171,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795531577","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1040589112","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503174,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140503174},{"seq_region_name":"7","id":"rs1795531626","clinical_significance":[],"start":140503183,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140503183,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503185,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140503185,"seq_region_name":"7","id":"rs1795531648","clinical_significance":[]},{"clinical_significance":[],"id":"rs2130422163","seq_region_name":"7","feature_type":"variation","strand":1,"end":140503186,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503186},{"alleles":["C","T"],"end":140503189,"feature_type":"variation","strand":1,"source":"dbSNP","start":140503189,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1257313154"},{"end":140503190,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140503190,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1042858103","seq_region_name":"7"},{"start":140503193,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140503193,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795531720","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503196,"source":"dbSNP","strand":1,"feature_type":"variation","end":140503196,"alleles":["G","A"],"seq_region_name":"7","id":"rs1183907763","clinical_significance":[]},{"clinical_significance":[],"id":"rs540427685","seq_region_name":"7","alleles":["T","C"],"end":140503197,"feature_type":"variation","strand":1,"source":"dbSNP","start":140503197,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs903108501","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503199,"source":"dbSNP","strand":1,"feature_type":"variation","end":140503199,"alleles":["G","A"]},{"alleles":["T","C"],"end":140503200,"feature_type":"variation","strand":1,"source":"dbSNP","start":140503200,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795531819"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795531846","source":"dbSNP","start":140503202,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140503202,"alleles":["G","A"],"feature_type":"variation","strand":1},{"id":"rs1315515288","seq_region_name":"7","clinical_significance":[],"end":140503203,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140503203,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs181092298","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503204,"source":"dbSNP","strand":1,"feature_type":"variation","end":140503204,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1031029049","clinical_significance":[],"start":140503209,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140503209,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140503211,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503211,"source":"dbSNP","seq_region_name":"7","id":"rs2130422183","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140503214,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503214,"clinical_significance":[],"id":"rs1795532188","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585522938","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503218,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140503218},{"end":140503235,"alleles":["TTTCTTTTTTCTTTTTT","TTTCTTTTTTCTTTTTTCTTTTTT"],"strand":1,"feature_type":"variation","start":140503219,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795532240","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1276148976","feature_type":"variation","strand":1,"end":140503221,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503221},{"end":140503222,"alleles":["C","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140503222,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs376774972"},{"seq_region_name":"7","id":"rs921247444","clinical_significance":[],"end":140503222,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140503222,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795532348","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140503225,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503225,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503225,"feature_type":"variation","strand":1,"end":140503233,"alleles":["TTTTCTTTT","TTTT"],"clinical_significance":[],"id":"rs1224792834","seq_region_name":"7"},{"alleles":["T","C"],"end":140503227,"strand":1,"feature_type":"variation","start":140503227,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1325429192","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795532430","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503228,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TCT","T"],"end":140503230},{"end":140503229,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140503229,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs947487645"},{"id":"rs1795532506","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503229,"source":"dbSNP","strand":1,"feature_type":"variation","end":140503229,"alleles":["C","-"]},{"seq_region_name":"7","id":"rs1461687313","clinical_significance":[],"strand":1,"feature_type":"variation","end":140503230,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503230,"source":"dbSNP"},{"seq_region_name":"7","id":"rs750376724","clinical_significance":[],"end":140503247,"alleles":["TTTTTTTTTTTTTTTTTT","TTTTTTTT","TTTTTTTTTT","TTTTTTTTTTT","TTTTTTTTTTTT","TTTTTTTTTTTTTT","TTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT"],"strand":1,"feature_type":"variation","start":140503230,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795532784","source":"dbSNP","start":140503232,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140503232,"alleles":["T","A"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503233,"source":"dbSNP","strand":1,"feature_type":"variation","end":140503233,"alleles":["T","C"],"seq_region_name":"7","id":"rs1207785809","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1369224676","source":"dbSNP","start":140503235,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140503235,"alleles":["T","C"],"feature_type":"variation","strand":1},{"end":140503236,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140503236,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1167136959","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1044352763","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503237,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140503237},{"clinical_significance":[],"id":"rs1472596509","seq_region_name":"7","alleles":["T","C"],"end":140503238,"feature_type":"variation","strand":1,"source":"dbSNP","start":140503238,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1183614395","end":140503240,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140503240,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs904082317","clinical_significance":[],"end":140503241,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140503241,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140503242,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503242,"clinical_significance":[],"seq_region_name":"7","id":"rs532656725"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503247,"source":"dbSNP","strand":1,"feature_type":"variation","end":140503247,"alleles":["T","G"],"id":"rs1585522979","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795533072","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503247,"feature_type":"variation","strand":1,"end":140503248,"alleles":["TG","-"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1170654612","feature_type":"variation","strand":1,"end":140503248,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503248},{"id":"rs1476862898","seq_region_name":"7","clinical_significance":[],"start":140503248,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140503248,"alleles":["G","-"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795533156","end":140503251,"alleles":["GAGA","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140503248,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140503249,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140503249,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1407497567"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795533202","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503249,"feature_type":"variation","strand":1,"end":140503249,"alleles":["A","-"]},{"seq_region_name":"7","id":"rs1795533225","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503250,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140503250},{"end":140503253,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140503253,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585522987"},{"seq_region_name":"7","id":"rs1416613001","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140503255,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503255,"source":"dbSNP"},{"seq_region_name":"7","id":"rs537988607","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503256,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140503256},{"clinical_significance":[],"seq_region_name":"7","id":"rs1332613171","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503257,"feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140503257},{"seq_region_name":"7","id":"rs1585522995","clinical_significance":[],"end":140503260,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140503260,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1585522998","clinical_significance":[],"alleles":["T","G"],"end":140503262,"strand":1,"feature_type":"variation","start":140503262,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs150776993","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503265,"source":"dbSNP","strand":1,"feature_type":"variation","end":140503265,"alleles":["C","T"]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140503266,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503266,"source":"dbSNP","seq_region_name":"7","id":"rs1246509429","clinical_significance":[]},{"start":140503269,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140503269,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1431083186","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140503271,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503271,"clinical_significance":[],"seq_region_name":"7","id":"rs1795533541"},{"seq_region_name":"7","id":"rs1585523013","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503272,"source":"dbSNP","strand":1,"feature_type":"variation","end":140503272,"alleles":["G","T"]},{"id":"rs1585523016","seq_region_name":"7","clinical_significance":[],"end":140503275,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140503275,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1292448420","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503279,"source":"dbSNP","strand":1,"feature_type":"variation","end":140503279,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs2130422288","clinical_significance":[],"alleles":["A","G"],"end":140503280,"strand":1,"feature_type":"variation","start":140503280,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140503282,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503282,"source":"dbSNP","id":"rs999877388","seq_region_name":"7","clinical_significance":[]},{"start":140503286,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140503286,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585523021","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795533702","source":"dbSNP","start":140503287,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140503287,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503288,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140503288,"seq_region_name":"7","id":"rs1337829350","clinical_significance":[]},{"end":140503289,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140503289,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1217461054","clinical_significance":[]},{"seq_region_name":"7","id":"rs1283314490","clinical_significance":[],"strand":1,"feature_type":"variation","end":140503293,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503293,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130422305","end":140503295,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140503295,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140503296,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503296,"source":"dbSNP","seq_region_name":"7","id":"rs1795533815","clinical_significance":[]},{"alleles":["A","G"],"end":140503297,"feature_type":"variation","strand":1,"source":"dbSNP","start":140503297,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1295565205"},{"clinical_significance":[],"seq_region_name":"7","id":"rs116785885","source":"dbSNP","start":140503299,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C","T"],"end":140503299,"feature_type":"variation","strand":1},{"id":"rs530317626","seq_region_name":"7","clinical_significance":[],"start":140503304,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140503304,"strand":1,"feature_type":"variation"},{"start":140503305,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140503305,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs548515947","clinical_significance":[]},{"clinical_significance":[],"id":"rs969421085","seq_region_name":"7","source":"dbSNP","start":140503306,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140503306,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1473870886","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140503315,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503315},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585523033","alleles":["A","C"],"end":140503316,"feature_type":"variation","strand":1,"source":"dbSNP","start":140503316,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503318,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140503318,"seq_region_name":"7","id":"rs1795534122","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs891554580","feature_type":"variation","strand":1,"end":140503319,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503319},{"start":140503321,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140503321,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs1181685242","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140503322,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503322,"source":"dbSNP","id":"rs1436771940","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503323,"feature_type":"variation","strand":1,"end":140503323,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1014413553"},{"seq_region_name":"7","id":"rs1795534295","clinical_significance":[],"start":140503324,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140503324,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140503326,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140503326,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1211337521"},{"source":"dbSNP","start":140503327,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140503327,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1466812958"},{"id":"rs746214232","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140503328,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503328,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs772551136","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140503329,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503329},{"strand":1,"feature_type":"variation","end":140503336,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503336,"source":"dbSNP","seq_region_name":"7","id":"rs1795534433","clinical_significance":[]},{"seq_region_name":"7","id":"rs567155636","clinical_significance":[],"end":140503338,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140503338,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140503339,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503339,"source":"dbSNP","id":"rs1277750661","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","C"],"end":140503341,"feature_type":"variation","strand":1,"source":"dbSNP","start":140503341,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795534523"},{"seq_region_name":"7","id":"rs1024170515","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503344,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140503344},{"start":140503345,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140503345,"alleles":["C","G"],"strand":1,"feature_type":"variation","id":"rs1795534591","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1217670108","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140503346,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503346,"source":"dbSNP"},{"end":140503350,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140503350,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs909353029","seq_region_name":"7","clinical_significance":[]},{"start":140503352,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140503352,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1331818041","clinical_significance":[]},{"seq_region_name":"7","id":"rs1303413175","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503354,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140503354},{"alleles":["T","G"],"end":140503357,"strand":1,"feature_type":"variation","start":140503357,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795534741","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503360,"feature_type":"variation","strand":1,"end":140503360,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795534765"},{"alleles":["T","G"],"end":140503361,"strand":1,"feature_type":"variation","start":140503361,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1439000339","clinical_significance":[]},{"source":"dbSNP","start":140503362,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140503362,"alleles":["A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795534819"},{"seq_region_name":"7","id":"rs1265576870","clinical_significance":[],"start":140503363,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140503363,"strand":1,"feature_type":"variation"},{"start":140503366,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140503366,"strand":1,"feature_type":"variation","id":"rs1795534877","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs962626549","clinical_significance":[],"strand":1,"feature_type":"variation","end":140503367,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503367,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585523059","end":140503368,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140503368,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503370,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140503370,"clinical_significance":[],"seq_region_name":"7","id":"rs1795534974"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140503373,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503373,"clinical_significance":[],"seq_region_name":"7","id":"rs1795535010"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503375,"feature_type":"variation","strand":1,"end":140503375,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130422375"},{"end":140503376,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140503376,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1321681931"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503377,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140503377,"clinical_significance":[],"seq_region_name":"7","id":"rs1795535059"},{"clinical_significance":[],"id":"rs11771430","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140503378,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503378},{"source":"dbSNP","start":140503379,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140503379,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1383235350"},{"seq_region_name":"7","id":"rs538793718","clinical_significance":[],"alleles":["C","A","T"],"end":140503380,"strand":1,"feature_type":"variation","start":140503380,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs933022941","source":"dbSNP","start":140503381,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140503381,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503383,"source":"dbSNP","strand":1,"feature_type":"variation","end":140503383,"alleles":["C","A","T"],"id":"rs1795535261","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs185532176","clinical_significance":[],"strand":1,"feature_type":"variation","end":140503384,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503384,"source":"dbSNP"},{"alleles":["G","A","T"],"end":140503385,"strand":1,"feature_type":"variation","start":140503385,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1171321157","clinical_significance":[]},{"source":"dbSNP","start":140503386,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140503386,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs910306161"},{"clinical_significance":[],"seq_region_name":"7","id":"rs983416608","alleles":["C","A","T"],"end":140503390,"feature_type":"variation","strand":1,"source":"dbSNP","start":140503390,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795535404","source":"dbSNP","start":140503391,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140503391,"feature_type":"variation","strand":1},{"start":140503392,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140503392,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs947125245","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503393,"feature_type":"variation","strand":1,"end":140503393,"alleles":["G","A"],"clinical_significance":[],"id":"rs1043296855","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795535484","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140503394,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503394},{"id":"rs1795535511","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503403,"source":"dbSNP","strand":1,"feature_type":"variation","end":140503408,"alleles":["TTTTTT","TTTTT"]},{"source":"dbSNP","start":140503404,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140503404,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1299709690"},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140503408,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503408,"source":"dbSNP","seq_region_name":"7","id":"rs1795535572","clinical_significance":[]},{"alleles":["G","A"],"end":140503409,"feature_type":"variation","strand":1,"source":"dbSNP","start":140503409,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1345557483"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795535629","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503410,"feature_type":"variation","strand":1,"end":140503410,"alleles":["T","C"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503411,"feature_type":"variation","strand":1,"end":140503411,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795535654"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1358257106","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503423,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140503423},{"seq_region_name":"7","id":"rs1398963928","clinical_significance":[],"start":140503424,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140503424,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1232129173","clinical_significance":[],"alleles":["T","C"],"end":140503425,"strand":1,"feature_type":"variation","start":140503425,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140503426,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140503426,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795535770"},{"seq_region_name":"7","id":"rs1563107115","clinical_significance":[],"start":140503427,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140503427,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1303238701","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503428,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140503428},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503429,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140503429,"clinical_significance":[],"seq_region_name":"7","id":"rs1298673107"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1437532125","source":"dbSNP","start":140503436,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140503436,"alleles":["T","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1325122631","clinical_significance":[],"end":140503438,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140503438,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs572269131","clinical_significance":[],"alleles":["T","A","C"],"end":140503441,"strand":1,"feature_type":"variation","start":140503441,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503442,"source":"dbSNP","strand":1,"feature_type":"variation","end":140503442,"alleles":["G","C"],"seq_region_name":"7","id":"rs1014878194","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503443,"source":"dbSNP","strand":1,"feature_type":"variation","end":140503443,"alleles":["G","A"],"seq_region_name":"7","id":"rs149959645","clinical_significance":[]},{"clinical_significance":[],"id":"rs1404921987","seq_region_name":"7","end":140503444,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140503444,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140503445,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503445,"clinical_significance":[],"seq_region_name":"7","id":"rs1795536082"},{"seq_region_name":"7","id":"rs902995020","clinical_significance":[],"start":140503448,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140503448,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140503452,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140503452,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795536147"},{"end":140503454,"alleles":["C","CC"],"strand":1,"feature_type":"variation","start":140503454,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs34916974","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs999078649","seq_region_name":"7","feature_type":"variation","strand":1,"end":140503456,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503456},{"clinical_significance":[],"seq_region_name":"7","id":"rs1393936992","alleles":["G","A"],"end":140503457,"feature_type":"variation","strand":1,"source":"dbSNP","start":140503457,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140503459,"alleles":["A","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140503459,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs976561835"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503463,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140503463,"seq_region_name":"7","id":"rs1450871877","clinical_significance":[]},{"end":140503464,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140503464,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs538765888","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795536388","alleles":["G","A"],"end":140503465,"feature_type":"variation","strand":1,"source":"dbSNP","start":140503465,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1585523119","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503466,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140503466},{"alleles":["CC","C"],"end":140503468,"feature_type":"variation","strand":1,"source":"dbSNP","start":140503467,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795536440"},{"feature_type":"variation","strand":1,"end":140503470,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503470,"clinical_significance":[],"id":"rs2130422469","seq_region_name":"7"},{"id":"rs1442965755","seq_region_name":"7","clinical_significance":[],"start":140503472,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140503472,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1795536493","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503473,"source":"dbSNP","strand":1,"feature_type":"variation","end":140503473,"alleles":["G","A"]},{"start":140503474,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140503474,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1280701603","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs922148319","end":140503475,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140503475,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140503476,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503476,"source":"dbSNP","seq_region_name":"7","id":"rs1795538012","clinical_significance":[]},{"alleles":["C","G"],"end":140503479,"strand":1,"feature_type":"variation","start":140503479,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795538030","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795538056","clinical_significance":[],"strand":1,"feature_type":"variation","end":140503485,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503485,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795538084","alleles":["C","T"],"end":140503486,"feature_type":"variation","strand":1,"source":"dbSNP","start":140503486,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140503487,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140503487,"alleles":["T","A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs556981096"},{"end":140503495,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140503495,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130422484","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503496,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140503496,"clinical_significance":[],"seq_region_name":"7","id":"rs1347322191"},{"seq_region_name":"7","id":"rs932161228","clinical_significance":[],"start":140503499,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140503499,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503502,"source":"dbSNP","strand":1,"feature_type":"variation","end":140503502,"alleles":["G","C"],"seq_region_name":"7","id":"rs2130422489","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795538177","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503512,"feature_type":"variation","strand":1,"end":140503512,"alleles":["C","T"]},{"clinical_significance":[],"id":"rs979568566","seq_region_name":"7","alleles":["G","A"],"end":140503515,"feature_type":"variation","strand":1,"source":"dbSNP","start":140503515,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795538240","alleles":["G","A"],"end":140503519,"feature_type":"variation","strand":1,"source":"dbSNP","start":140503519,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140503522,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140503522,"alleles":["C","A"],"strand":1,"feature_type":"variation","id":"rs1337633830","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","T"],"end":140503523,"feature_type":"variation","strand":1,"source":"dbSNP","start":140503523,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1270005960"},{"seq_region_name":"7","id":"rs1795538307","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503525,"source":"dbSNP","strand":1,"feature_type":"variation","end":140503525,"alleles":["C","T"]},{"source":"dbSNP","start":140503525,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140503526,"alleles":["CC","CCC"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs370229590"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503526,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140503526,"clinical_significance":[],"seq_region_name":"7","id":"rs1268215531"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140503528,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503528,"source":"dbSNP","seq_region_name":"7","id":"rs1795538408","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140503533,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503533,"clinical_significance":[],"seq_region_name":"7","id":"rs1585523138"},{"seq_region_name":"7","id":"rs1795538456","clinical_significance":[],"strand":1,"feature_type":"variation","end":140503537,"alleles":["T","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503537,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503538,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140503538,"seq_region_name":"7","id":"rs1057102345","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503541,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140503541,"clinical_significance":[],"seq_region_name":"7","id":"rs1795538528"},{"alleles":["C","G"],"end":140503546,"strand":1,"feature_type":"variation","start":140503546,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795538556","clinical_significance":[]},{"start":140503549,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140503549,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1311651098","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503551,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140503551,"clinical_significance":[],"seq_region_name":"7","id":"rs1795538624"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503554,"feature_type":"variation","strand":1,"end":140503554,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs895731247"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503555,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140503555,"id":"rs1795538696","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","T"],"end":140503556,"strand":1,"feature_type":"variation","start":140503556,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795538722","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["AAAAA","AAAA"],"end":140503561,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503557,"source":"dbSNP","seq_region_name":"7","id":"rs1795538748","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","C","T"],"end":140503560,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503560,"source":"dbSNP","id":"rs748357806","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503562,"source":"dbSNP","strand":1,"feature_type":"variation","end":140503562,"alleles":["C","T"],"seq_region_name":"7","id":"rs190333900","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503563,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140503563,"id":"rs561359190","seq_region_name":"7","clinical_significance":[]},{"id":"rs374670208","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503564,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140503564},{"feature_type":"variation","strand":1,"end":140503565,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503565,"clinical_significance":[],"id":"rs542941448","seq_region_name":"7"},{"alleles":["A","C"],"end":140503570,"feature_type":"variation","strand":1,"source":"dbSNP","start":140503570,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795538995","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795539018","clinical_significance":[],"strand":1,"feature_type":"variation","end":140503570,"alleles":["A","AA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503570,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1166926559","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503571,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140503571},{"clinical_significance":[],"seq_region_name":"7","id":"rs1473032236","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503572,"feature_type":"variation","strand":1,"end":140503572,"alleles":["T","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1016742651","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503576,"feature_type":"variation","strand":1,"end":140503576,"alleles":["G","C"]},{"start":140503577,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140503577,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs554522671","clinical_significance":[]},{"end":140503578,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140503578,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs117486495"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795539241","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503579,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140503579},{"alleles":["A","G"],"end":140503582,"strand":1,"feature_type":"variation","start":140503582,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795539267","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795539291","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503584,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140503584},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503589,"source":"dbSNP","strand":1,"feature_type":"variation","end":140503589,"alleles":["A","G"],"seq_region_name":"7","id":"rs1795539316","clinical_significance":[]},{"seq_region_name":"7","id":"rs1440796838","clinical_significance":[],"alleles":["A","T"],"end":140503591,"strand":1,"feature_type":"variation","start":140503591,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795539374","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503594,"feature_type":"variation","strand":1,"end":140503594,"alleles":["A","T"]},{"strand":1,"feature_type":"variation","end":140503595,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503595,"source":"dbSNP","seq_region_name":"7","id":"rs147664961","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795539457","clinical_significance":[],"start":140503604,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140503604,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1252646339","clinical_significance":[],"start":140503605,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140503605,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1001780676","end":140503606,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140503606,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140503609,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503609,"source":"dbSNP","seq_region_name":"7","id":"rs772336886","clinical_significance":[]},{"end":140503612,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140503612,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1207324276","clinical_significance":[]},{"alleles":["TTTACTTTA","TTTA"],"end":140503621,"strand":1,"feature_type":"variation","start":140503613,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1436325685","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1378787006","source":"dbSNP","start":140503615,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140503615,"feature_type":"variation","strand":1},{"end":140503617,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140503617,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795539670","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503622,"feature_type":"variation","strand":1,"end":140503622,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1229085840"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795539855","end":140503625,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140503625,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795539877","alleles":["T","C"],"end":140503628,"feature_type":"variation","strand":1,"source":"dbSNP","start":140503628,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140503634,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140503634,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795539901"},{"alleles":["A","T"],"end":140503638,"strand":1,"feature_type":"variation","start":140503638,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1585523200","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs923565015","clinical_significance":[],"strand":1,"feature_type":"variation","end":140503640,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503640,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1795539983","seq_region_name":"7","source":"dbSNP","start":140503646,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140503646,"alleles":["A","G"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503647,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140503647,"clinical_significance":[],"seq_region_name":"7","id":"rs1795540004"},{"clinical_significance":[],"id":"rs1358980927","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503650,"feature_type":"variation","strand":1,"end":140503650,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1795540049","clinical_significance":[],"start":140503651,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C","G"],"end":140503651,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130422619","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140503654,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503654},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140503660,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503660,"source":"dbSNP","seq_region_name":"7","id":"rs954920897","clinical_significance":[]},{"alleles":["C","T"],"end":140503662,"strand":1,"feature_type":"variation","start":140503662,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1233220087","clinical_significance":[]},{"source":"dbSNP","start":140503663,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140503663,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795540108"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130422623","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503664,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140503664},{"seq_region_name":"7","id":"rs1351586076","clinical_significance":[],"start":140503667,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140503667,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140503668,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503668,"source":"dbSNP","seq_region_name":"7","id":"rs1163817044","clinical_significance":[]},{"seq_region_name":"7","id":"rs565112529","clinical_significance":[],"start":140503669,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140503669,"strand":1,"feature_type":"variation"},{"start":140503669,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AAAAAAAA","AAAAAAA","AAAAAAAAA"],"end":140503676,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs773560457","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140503671,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503671,"clinical_significance":[],"seq_region_name":"7","id":"rs1795540219"},{"clinical_significance":[],"id":"rs1563107170","seq_region_name":"7","feature_type":"variation","strand":1,"end":140503676,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503676},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503679,"feature_type":"variation","strand":1,"end":140503679,"alleles":["T","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585523233"},{"seq_region_name":"7","id":"rs1795540272","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140503684,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503684,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795540289","alleles":["T","C"],"end":140503686,"feature_type":"variation","strand":1,"source":"dbSNP","start":140503686,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140503687,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140503687,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795540314","clinical_significance":[]},{"start":140503689,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140503689,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585523249","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs142377415","alleles":["C","T"],"end":140503693,"feature_type":"variation","strand":1,"source":"dbSNP","start":140503693,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503694,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140503694,"clinical_significance":[],"seq_region_name":"7","id":"rs1384542862"},{"seq_region_name":"7","id":"rs1795540402","clinical_significance":[],"end":140503696,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140503696,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1585523251","seq_region_name":"7","end":140503697,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140503697,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503700,"source":"dbSNP","strand":1,"feature_type":"variation","end":140503700,"alleles":["A","G"],"seq_region_name":"7","id":"rs2130422655","clinical_significance":[]},{"seq_region_name":"7","id":"rs1405590829","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503705,"source":"dbSNP","strand":1,"feature_type":"variation","end":140503705,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1419768110","alleles":["G","A","T"],"end":140503706,"feature_type":"variation","strand":1,"source":"dbSNP","start":140503706,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140503712,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503712,"clinical_significance":[],"seq_region_name":"7","id":"rs1795540476"},{"seq_region_name":"7","id":"rs1014909566","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140503713,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503713,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1795540522","seq_region_name":"7","alleles":["A","G"],"end":140503714,"feature_type":"variation","strand":1,"source":"dbSNP","start":140503714,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140503717,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140503717,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130422669"},{"strand":1,"feature_type":"variation","end":140503719,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503719,"source":"dbSNP","id":"rs1795540539","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140503722,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503722,"source":"dbSNP","seq_region_name":"7","id":"rs1322249645","clinical_significance":[]},{"id":"rs1474853958","seq_region_name":"7","clinical_significance":[],"start":140503726,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140503726,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585523270","source":"dbSNP","start":140503730,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140503730,"feature_type":"variation","strand":1},{"alleles":["C","T"],"end":140503731,"feature_type":"variation","strand":1,"source":"dbSNP","start":140503731,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795540613"},{"strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140503737,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503737,"source":"dbSNP","id":"rs1412576564","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503739,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140503739,"clinical_significance":[],"id":"rs1178851306","seq_region_name":"7"},{"end":140503741,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140503741,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1448811255","clinical_significance":[]},{"source":"dbSNP","start":140503742,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140503742,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795540707"},{"feature_type":"variation","strand":1,"end":140503743,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503743,"clinical_significance":[],"seq_region_name":"7","id":"rs1795540725"},{"end":140503744,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140503744,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1306823722"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503745,"feature_type":"variation","strand":1,"end":140503745,"alleles":["A","AAAA"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795540768"},{"clinical_significance":[],"id":"rs1352698659","seq_region_name":"7","source":"dbSNP","start":140503746,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140503746,"alleles":["T","A","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs966424433","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503747,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","T"],"end":140503747},{"seq_region_name":"7","id":"rs1266227735","clinical_significance":[],"alleles":["T","A","C"],"end":140503749,"strand":1,"feature_type":"variation","start":140503749,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["TT","TTT"],"end":140503750,"feature_type":"variation","strand":1,"source":"dbSNP","start":140503749,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1271684804"},{"id":"rs1795540886","seq_region_name":"7","clinical_significance":[],"start":140503750,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140503749,"alleles":["-","A","C"],"strand":1,"feature_type":"variation"},{"start":140503750,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140503750,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","id":"rs1213413402","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140503751,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["-","TA"],"end":140503750,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795540936"},{"feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140503751,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503751,"clinical_significance":[],"seq_region_name":"7","id":"rs1795540955"},{"alleles":["AAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAA","AAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAA"],"end":140503768,"feature_type":"variation","strand":1,"source":"dbSNP","start":140503751,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs34173812"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1318913796","source":"dbSNP","start":140503758,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140503757,"alleles":["-","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795541141","source":"dbSNP","start":140503758,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140503758,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1585523295","seq_region_name":"7","source":"dbSNP","start":140503764,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140503764,"alleles":["A","G"],"feature_type":"variation","strand":1},{"id":"rs1795541181","seq_region_name":"7","clinical_significance":[],"end":140503765,"alleles":["-","C"],"strand":1,"feature_type":"variation","start":140503766,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140503768,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140503767,"alleles":["-","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1358625423","clinical_significance":[]},{"seq_region_name":"7","id":"rs576024175","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503768,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140503768},{"seq_region_name":"7","id":"rs1563107190","clinical_significance":[],"alleles":["-","T"],"end":140503768,"strand":1,"feature_type":"variation","start":140503769,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503769,"source":"dbSNP","strand":1,"feature_type":"variation","end":140503769,"alleles":["G","A","C"],"id":"rs976088220","seq_region_name":"7","clinical_significance":[]},{"start":140503769,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140503770,"alleles":["GG","GGG"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1563107192","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1289191433","source":"dbSNP","start":140503770,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140503770,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs12673419","clinical_significance":[],"end":140503771,"alleles":["A","C","T"],"strand":1,"feature_type":"variation","start":140503771,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1029505171","source":"dbSNP","start":140503772,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140503772,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140503782,"alleles":["CGGTGTGTGGT","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503772,"clinical_significance":[],"id":"rs1554454508","seq_region_name":"7"},{"end":140503773,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140503773,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1180992701","seq_region_name":"7","clinical_significance":[]},{"end":140503774,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140503774,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795541389","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs998677102","clinical_significance":[],"start":140503775,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140503775,"alleles":["T","A","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795541443","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503776,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140503776},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503777,"feature_type":"variation","strand":1,"end":140503777,"alleles":["T","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585523325"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503778,"feature_type":"variation","strand":1,"end":140503778,"alleles":["G","T"],"clinical_significance":[],"id":"rs2130422765","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503779,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140503779,"seq_region_name":"7","id":"rs112128200","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1439469734","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503781,"feature_type":"variation","strand":1,"end":140503781,"alleles":["G","A"]},{"id":"rs1057424271","seq_region_name":"7","clinical_significance":[],"end":140503782,"alleles":["T","A","G"],"strand":1,"feature_type":"variation","start":140503782,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["A","G"],"end":140503783,"strand":1,"feature_type":"variation","start":140503783,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1193214547","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503787,"feature_type":"variation","strand":1,"end":140503787,"alleles":["T","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1465676704"},{"clinical_significance":[],"id":"rs2130422784","seq_region_name":"7","feature_type":"variation","strand":1,"end":140503788,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503788},{"seq_region_name":"7","id":"rs1262859542","clinical_significance":[],"strand":1,"feature_type":"variation","end":140503791,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503791,"source":"dbSNP"},{"end":140503792,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140503792,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs979599675"},{"seq_region_name":"7","id":"rs1795541653","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503797,"source":"dbSNP","strand":1,"feature_type":"variation","end":140503797,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs535948681","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140503798,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503798,"source":"dbSNP"},{"source":"dbSNP","start":140503799,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140503799,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1585523340","seq_region_name":"7"},{"clinical_significance":[],"id":"rs895764352","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140503802,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503802},{"alleles":["T","C","G"],"end":140503808,"strand":1,"feature_type":"variation","start":140503808,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795541736","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140503810,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503810,"clinical_significance":[],"seq_region_name":"7","id":"rs1585523344"},{"alleles":["C","T"],"end":140503812,"strand":1,"feature_type":"variation","start":140503812,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1282972771","clinical_significance":[]},{"alleles":["C","T"],"end":140503813,"strand":1,"feature_type":"variation","start":140503813,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795541805","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140503814,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503814,"source":"dbSNP","seq_region_name":"7","id":"rs1219268367","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795541837","source":"dbSNP","start":140503815,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140503815,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503817,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","G"],"end":140503817,"seq_region_name":"7","id":"rs1585523354","clinical_significance":[]},{"source":"dbSNP","start":140503822,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140503822,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1369857291","seq_region_name":"7"},{"start":140503822,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140503823,"alleles":["CC","CCCC"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1372503012","clinical_significance":[]},{"start":140503823,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140503823,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585523362","clinical_significance":[]},{"seq_region_name":"7","id":"rs1365662278","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503824,"source":"dbSNP","strand":1,"feature_type":"variation","end":140503824,"alleles":["A","G"]},{"strand":1,"feature_type":"variation","end":140503828,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503828,"source":"dbSNP","seq_region_name":"7","id":"rs1290351422","clinical_significance":[]},{"start":140503829,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140503829,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs925440239","clinical_significance":[]},{"clinical_significance":[],"id":"rs1344492316","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503830,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140503830},{"alleles":["A","G"],"end":140503831,"feature_type":"variation","strand":1,"source":"dbSNP","start":140503831,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1176661234"},{"id":"rs1795542035","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503832,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140503832},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585523368","source":"dbSNP","start":140503833,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140503833,"alleles":["C","A"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503837,"feature_type":"variation","strand":1,"end":140503843,"alleles":["TTGTTTT","TT"],"clinical_significance":[],"id":"rs1795542071","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503839,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140503839,"seq_region_name":"7","id":"rs1436713095","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795542131","seq_region_name":"7","end":140503840,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140503840,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["T","A"],"end":140503842,"feature_type":"variation","strand":1,"source":"dbSNP","start":140503842,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1162128948"},{"end":140503849,"alleles":["TTATCTGA","TTATCTGATTATCTGA"],"strand":1,"feature_type":"variation","start":140503842,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795542173","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1173320607","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140503843,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503843},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585523376","source":"dbSNP","start":140503846,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140503846,"alleles":["C","A"],"feature_type":"variation","strand":1},{"start":140503850,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140503850,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130422850","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140503851,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503851,"clinical_significance":[],"seq_region_name":"7","id":"rs1585523380"},{"start":140503852,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A","C","G"],"end":140503852,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs79288441","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795542255","feature_type":"variation","strand":1,"end":140503854,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503854},{"alleles":["T","C"],"end":140503855,"strand":1,"feature_type":"variation","start":140503855,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795542294","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1264316443","seq_region_name":"7","alleles":["T","A","G"],"end":140503856,"feature_type":"variation","strand":1,"source":"dbSNP","start":140503856,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1485846298","clinical_significance":[],"start":140503857,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140503857,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140503860,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503860,"clinical_significance":[],"seq_region_name":"7","id":"rs1238600969"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585523395","alleles":["G","A"],"end":140503863,"feature_type":"variation","strand":1,"source":"dbSNP","start":140503863,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140503867,"alleles":["G","A","C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140503867,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1213622012"},{"start":140503869,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140503869,"alleles":["C","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130422876","clinical_significance":[]},{"start":140503869,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["CTTTCAGCCTCTC","-"],"end":140503881,"strand":1,"feature_type":"variation","id":"rs1795542462","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795542488","seq_region_name":"7","alleles":["T","G"],"end":140503872,"feature_type":"variation","strand":1,"source":"dbSNP","start":140503872,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140503873,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503873,"clinical_significance":[],"seq_region_name":"7","id":"rs1795542522"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1349498676","alleles":["AGCCTCTCAAAAAAAAAAAAAAAAAAAGA","A"],"end":140503902,"feature_type":"variation","strand":1,"source":"dbSNP","start":140503874,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1277572790","seq_region_name":"7","alleles":["C","A","T"],"end":140503876,"feature_type":"variation","strand":1,"source":"dbSNP","start":140503876,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140503877,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["CTCTC","CTC"],"end":140503881,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795542607","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585523401","clinical_significance":[],"strand":1,"feature_type":"variation","end":140503878,"alleles":["T","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503878,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1233121017","feature_type":"variation","strand":1,"end":140503879,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503879},{"clinical_significance":[],"id":"rs1585523406","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503880,"feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140503880},{"seq_region_name":"7","id":"rs1795542705","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","-"],"end":140503880,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503880,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140503881,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503881,"source":"dbSNP","seq_region_name":"7","id":"rs1307665597","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503881,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","-"],"end":140503881,"seq_region_name":"7","id":"rs1795542775","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1190698894","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503882,"feature_type":"variation","strand":1,"alleles":["AAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAA","AAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA"],"end":140503900},{"start":140503886,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AAAAAAAAAA","AAAAAAAAAAGAAAAAAAAAA"],"end":140503895,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1254845425","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795543167","clinical_significance":[],"start":140503888,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AAAAAAA","AAAAAAAGAAAAAAA"],"end":140503894,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503890,"feature_type":"variation","strand":1,"end":140503890,"alleles":["A","G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795543187"},{"id":"rs1795543209","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140503893,"alleles":["AAAA","AAAAGAAAA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503890,"source":"dbSNP"},{"start":140503891,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140503891,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1209492727","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795543272","alleles":["AAAAA","AAAAAGAAAAA"],"end":140503895,"feature_type":"variation","strand":1,"source":"dbSNP","start":140503891,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs2130422928","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503892,"source":"dbSNP","strand":1,"feature_type":"variation","end":140503891,"alleles":["-","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1480652442","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503892,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140503892},{"seq_region_name":"7","id":"rs1795543325","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["AAA","AAAGAAA"],"end":140503894,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503892,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795543353","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["AAAAAAAAGAAAAGAAAGAAAGAAAAAGAAAAA","AAAAA"],"end":140503925,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503893,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795543386","end":140503894,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140503894,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["AAAAAAAGAAAAGAAAGAAAGAAAAAGAAAAA","AAAAA"],"end":140503925,"strand":1,"feature_type":"variation","start":140503894,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1329219754","clinical_significance":[]},{"id":"rs1375925931","seq_region_name":"7","clinical_significance":[],"end":140503894,"alleles":["-","G"],"strand":1,"feature_type":"variation","start":140503895,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140503925,"alleles":["AAAAAAGAAAAGAAAGAAAGAAAAAGAAAAA","AAAAA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503895,"clinical_significance":[],"seq_region_name":"7","id":"rs1795543452"},{"seq_region_name":"7","id":"rs1453069391","clinical_significance":[],"start":140503896,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140503895,"alleles":["-","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs112363246","clinical_significance":[],"end":140503896,"alleles":["A","C","G","T"],"strand":1,"feature_type":"variation","start":140503896,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1795543539","seq_region_name":"7","clinical_significance":[],"start":140503896,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140503905,"alleles":["AAAAAGAAAA","AAAA"],"strand":1,"feature_type":"variation"},{"start":140503896,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140503924,"alleles":["AAAAAGAAAAGAAAGAAAGAAAAAGAAAA","AAAAAGAAAA"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795543554","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140503925,"alleles":["AAAAAGAAAAGAAAGAAAGAAAAAGAAAAA","AAAAA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503896,"clinical_significance":[],"seq_region_name":"7","id":"rs1795543572"},{"start":140503897,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140503896,"alleles":["-","G","GAAAAAAG","GAAAAAG","GAAAAGAAAAG"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1554454545","clinical_significance":[]},{"clinical_significance":[],"id":"rs1554454543","seq_region_name":"7","source":"dbSNP","start":140503897,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","AGA","AGAAAAAAAAGA","AGAAAAAAGA","AGAAAAAGA","AGAAAAGA"],"end":140503897,"feature_type":"variation","strand":1},{"alleles":["A","G"],"end":140503897,"strand":1,"feature_type":"variation","start":140503897,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795543613","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1554454546","source":"dbSNP","start":140503897,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140503898,"alleles":["AA","AAGAA","AAGAAAAGAA"],"feature_type":"variation","strand":1},{"start":140503897,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AAA","AAAGAAA","AAAGAAAGAAA"],"end":140503899,"strand":1,"feature_type":"variation","id":"rs1554454547","seq_region_name":"7","clinical_significance":[]},{"alleles":["AAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAACAAGAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAACAAAAAAAGAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAACAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAGAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAATAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAGAAAA","AAAAAAAAAAAAAAAAAAAAAAAAGAAAA","AAAAAAAAAAAAAAAAAAAAAAAGAAAA","AAAAAAAAAAAAAAAAAAAAAAATAAAA","AAAAAAAAAAAAAAAAAAAAAAGAAAA","AAAAAAAAAAAAAAAAAAAAAGAAAA","AAAAAAAAAAAAAAAAAAAAGAAAA","AAAAAAAAAAAAAAAAAAAGAAAA","AAAAAAAAAAAAAAAAAAGAAAA","AAAAAAAAAAAAAAAAAGAAAA","AAAAAAAAAAAAAAAAAGAAAGAAAGAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAA","AAAAAAAAAAAAAAAAGAAAA","AAAAAAAAAAAAAAAGAAAA","AAAAAAAAAAAAAAGAAAA","AAAAAAAAAAAAAGAAAA","AAAAAAAAAAAAGAAAA","AAAAAAAAAAAGAAAA","AAAAAAAAAAGAAAA","AAAAAAAAAGAAAA","AAAAAAAAGAAAA","AAAAAAAGAAAA","AAAAAAAGAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAA","AAAAAAAGAAAAGAAAAAAAAAAAGAAAA","AAAAAAAGAAAGAAAA","AAAAAAGAAAA","AAAAACAAAAAAAAAAGAAAA","AAAAAGAAAA","AAAAAGAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAA","AAAAAGAAAAGAAAA"],"end":140503900,"strand":1,"feature_type":"variation","start":140503897,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs781346966","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795544021","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["AAAAGAAAA","AAAAGAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAAGAAAA"],"end":140503905,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503897,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1554454544","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503897,"feature_type":"variation","strand":1,"end":140503909,"alleles":["AAAAGAAAAGAAA","AAAAGAAAAGAAAAGAAA","AAAAGAAAAGAAAAGAAAAGAAA"]},{"source":"dbSNP","start":140503897,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140503913,"alleles":["AAAAGAAAAGAAAGAAA","AAAAGAAAAGAAAGAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAAGAAAAGAAAGAAA"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795544117"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503897,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AAAAGAAAAGAAAGAAAGAAAA","AAAA"],"end":140503918,"id":"rs1273634702","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795544182","clinical_significance":[],"strand":1,"feature_type":"variation","end":140503924,"alleles":["AAAAGAAAAGAAAGAAAGAAAAAGAAAA","AAAA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503897,"source":"dbSNP"},{"start":140503897,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AAAAGAAAAGAAAGAAAGAAAAAGAAAAA","AAAAGAAAAGAAAGAAAGAAAAAGAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAAGAAAAGAAAGAAAGAAAAAGAAAAA"],"end":140503925,"strand":1,"feature_type":"variation","id":"rs1795544200","seq_region_name":"7","clinical_significance":[]},{"alleles":["-","GG","T"],"end":140503897,"feature_type":"variation","strand":1,"source":"dbSNP","start":140503898,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1215301016"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563107258","feature_type":"variation","strand":1,"end":140503900,"alleles":["AAA","AAAAAAAAAAAAAAAAAAAAAAATAAA","AAAAAAAAAAAAAAAAAAAAGGAAA","AAAAAAAAAAAAAAAAAAGGAAA","AAAAAAAAAAAAAAAAAGGAAA","AAAAAAAAAAAAAAAAGGAAA","AAAAAAAAAAGGAAA","AAAAAAAAAGGAAA","AAAAAAGGAAA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503898},{"seq_region_name":"7","id":"rs1795544307","clinical_significance":[],"start":140503898,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140503904,"alleles":["AAAGAAA","AAA"],"strand":1,"feature_type":"variation"},{"end":140503917,"alleles":["AAAGAAAAGAAAGAAAGAAA","AAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140503898,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795544324"},{"strand":1,"feature_type":"variation","end":140503923,"alleles":["AAAGAAAAGAAAGAAAGAAAAAGAAA","AAA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503898,"source":"dbSNP","seq_region_name":"7","id":"rs1795544343","clinical_significance":[]},{"alleles":["-","GAG"],"end":140503898,"strand":1,"feature_type":"variation","start":140503899,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1332354619","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503899,"feature_type":"variation","strand":1,"end":140503903,"alleles":["AAGAA","AA"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795544385"},{"clinical_significance":[],"id":"rs1795544407","seq_region_name":"7","source":"dbSNP","start":140503899,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AAGAAAAGAA","AA"],"end":140503908,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795544438","source":"dbSNP","start":140503899,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140503912,"alleles":["AAGAAAAGAAAGAA","AA"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503900,"feature_type":"variation","strand":1,"end":140503902,"alleles":["AGA","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1314552035"},{"seq_region_name":"7","id":"rs1239604963","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503900,"source":"dbSNP","strand":1,"feature_type":"variation","end":140503907,"alleles":["AGAAAAGA","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795544534","alleles":["AGAAAAGAAAGAAAGAAAAAGA","A"],"end":140503921,"feature_type":"variation","strand":1,"source":"dbSNP","start":140503900,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140503901,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140503900,"alleles":["-","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAC","AAAAAAAAAAAAAAAAAAAAAT"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795544559"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503901,"feature_type":"variation","strand":1,"end":140503901,"alleles":["G","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs200142537"},{"id":"rs1432983287","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503901,"source":"dbSNP","strand":1,"feature_type":"variation","end":140503901,"alleles":["G","-"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795544656","feature_type":"variation","strand":1,"end":140503906,"alleles":["GAAAAG","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503901},{"end":140503910,"alleles":["GAAAAGAAAG","-"],"strand":1,"feature_type":"variation","start":140503901,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1337614308","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795544700","source":"dbSNP","start":140503901,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140503914,"alleles":["GAAAAGAAAGAAAG","-"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1304947649","clinical_significance":[],"start":140503901,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140503920,"alleles":["GAAAAGAAAGAAAGAAAAAG","-"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140503926,"alleles":["GAAAAGAAAGAAAGAAAAAGAAAAAT","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503901,"source":"dbSNP","seq_region_name":"7","id":"rs1795544758","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140503902,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503902,"clinical_significance":[],"seq_region_name":"7","id":"rs1795544783"},{"end":140503903,"alleles":["AA","AACAAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140503902,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795544810"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503902,"feature_type":"variation","strand":1,"alleles":["AAAA","AAA","AAAAA","AAAAAAA","AAAAAAAAA","AAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAA"],"end":140503905,"clinical_significance":[],"seq_region_name":"7","id":"rs1328127920"},{"seq_region_name":"7","id":"rs1795544904","clinical_significance":[],"start":140503902,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AAAA","-"],"end":140503905,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795544943","alleles":["-","GAAAAG"],"end":140503902,"feature_type":"variation","strand":1,"source":"dbSNP","start":140503903,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140503903,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAGAAA","AAAAGAAAAGAAA"],"end":140503905,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795544966","clinical_significance":[]},{"start":140503903,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AAAGAAA","AAAGAAAAGAAAGAAA"],"end":140503909,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1554454556","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503903,"feature_type":"variation","strand":1,"end":140503917,"alleles":["AAAGAAAGAAAGAAA","AAAGAAAGAAAGAAAGAAA"],"clinical_significance":[],"seq_region_name":"7","id":"rs1460228565"},{"seq_region_name":"7","id":"rs1795545081","clinical_significance":[],"start":140503903,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140503923,"alleles":["AAAGAAAGAAAGAAAAAGAAA","AAA"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140503922,"alleles":["AAGAAAGAAAGAAAAAGAA","AA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503904,"source":"dbSNP","seq_region_name":"7","id":"rs1342519020","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503905,"feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140503905,"clinical_significance":[],"id":"rs1160560808","seq_region_name":"7"},{"source":"dbSNP","start":140503905,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AGAAAGAAAGAAAAAGA","A"],"end":140503921,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1242796822"},{"seq_region_name":"7","id":"rs1795545207","clinical_significance":[],"start":140503906,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140503905,"alleles":["-","AAAAAG","AAAG"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs963004799","feature_type":"variation","strand":1,"end":140503906,"alleles":["G","A","C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503906},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563107265","feature_type":"variation","strand":1,"alleles":["G","-"],"end":140503906,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503906},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503906,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","GG"],"end":140503906,"seq_region_name":"7","id":"rs1795545295","clinical_significance":[]},{"id":"rs1795545348","seq_region_name":"7","clinical_significance":[],"alleles":["GAAA","GAAACGAAA"],"end":140503909,"strand":1,"feature_type":"variation","start":140503906,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1365095132","seq_region_name":"7","clinical_significance":[],"alleles":["GAAAG","-"],"end":140503910,"strand":1,"feature_type":"variation","start":140503906,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140503914,"alleles":["GAAAGAAAG","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503906,"source":"dbSNP","seq_region_name":"7","id":"rs1563107267","clinical_significance":[]},{"start":140503906,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["GAAAGAAAGAAAAAG","-"],"end":140503920,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795545460","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1418188768","feature_type":"variation","strand":1,"end":140503909,"alleles":["AAA","AAAA","AAAAA","AAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAACAAA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503907},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503907,"feature_type":"variation","strand":1,"end":140503918,"alleles":["AAAGAAAGAAAA","AAA"],"clinical_significance":[],"seq_region_name":"7","id":"rs1563107269"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503908,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AA","AAAGAAAAGAAAAGGAA"],"end":140503909,"seq_region_name":"7","id":"rs1795545610","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795545642","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["-","AAAAAC"],"end":140503909,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503910,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140503910,"alleles":["G","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503910,"clinical_significance":[],"seq_region_name":"7","id":"rs994551915"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503910,"feature_type":"variation","strand":1,"end":140503910,"alleles":["G","-"],"clinical_significance":[],"id":"rs1563107272","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["GAAAG","-"],"end":140503914,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503910,"clinical_significance":[],"seq_region_name":"7","id":"rs1282585189"},{"clinical_significance":[],"id":"rs1795545771","seq_region_name":"7","alleles":["GAAAGAAAAAG","-"],"end":140503920,"feature_type":"variation","strand":1,"source":"dbSNP","start":140503910,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503911,"feature_type":"variation","strand":1,"alleles":["AAA","AAAA"],"end":140503913,"clinical_significance":[],"seq_region_name":"7","id":"rs1795545802"},{"id":"rs1795545827","seq_region_name":"7","clinical_significance":[],"alleles":["AAAGAAAA","AAA"],"end":140503918,"strand":1,"feature_type":"variation","start":140503911,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563107276","source":"dbSNP","start":140503913,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AGA","A"],"end":140503915,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140503914,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140503914,"alleles":["G","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs754445309","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503914,"feature_type":"variation","strand":1,"end":140503914,"alleles":["G","A","C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1026023077"},{"seq_region_name":"7","id":"rs1563107282","clinical_significance":[],"start":140503915,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140503919,"alleles":["AAAAA","AAA","AAAA","AAAAAA"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1205710703","alleles":["A","G","T"],"end":140503916,"feature_type":"variation","strand":1,"source":"dbSNP","start":140503916,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs935597674","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503917,"feature_type":"variation","strand":1,"end":140503917,"alleles":["A","G","T"]},{"seq_region_name":"7","id":"rs1795546064","clinical_significance":[],"start":140503917,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AA","AAGAA"],"end":140503918,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503917,"feature_type":"variation","strand":1,"end":140503935,"alleles":["AAAGAAAAATAAAGAAAAA","AAAGAAAAA"],"clinical_significance":[],"id":"rs531074110","seq_region_name":"7"},{"end":140503922,"alleles":["AAGAA","AA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140503918,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795546123"},{"end":140503919,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140503919,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1238465483","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140503921,"alleles":["AGA","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503919,"clinical_significance":[],"seq_region_name":"7","id":"rs1318686582"},{"seq_region_name":"7","id":"rs747704025","clinical_significance":[],"strand":1,"feature_type":"variation","end":140503920,"alleles":["G","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503920,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503920,"feature_type":"variation","strand":1,"alleles":["G","A","C","T"],"end":140503920,"clinical_significance":[],"seq_region_name":"7","id":"rs951647912"},{"seq_region_name":"7","id":"rs1256685110","clinical_significance":[],"strand":1,"feature_type":"variation","end":140503921,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503921,"source":"dbSNP"},{"start":140503921,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140503925,"alleles":["AAAAA","AAAAAAAA","AAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAGAAAAAAAAAAAAAAAAAAA"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795546339","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795546385","clinical_significance":[],"start":140503922,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140503921,"alleles":["-","T"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503922,"feature_type":"variation","strand":1,"end":140503922,"alleles":["A","T"],"clinical_significance":[],"id":"rs1370813199","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1795546449","seq_region_name":"7","alleles":["AA","AATAA"],"end":140503923,"feature_type":"variation","strand":1,"source":"dbSNP","start":140503922,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140503942,"alleles":["AAAATAAAGAAAAAAAAAGAA","AA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503922,"source":"dbSNP","seq_region_name":"7","id":"rs1795546482","clinical_significance":[]},{"seq_region_name":"7","id":"rs1457670041","clinical_significance":[],"start":140503923,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140503923,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1563107299","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503923,"feature_type":"variation","strand":1,"alleles":["A","ATA"],"end":140503923},{"alleles":["AAA","AAAAAAAAAAAAAAACAAAAAAAAAAAGAAA"],"end":140503925,"strand":1,"feature_type":"variation","start":140503923,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795546575","clinical_significance":[]},{"seq_region_name":"7","id":"rs1319377003","clinical_significance":[],"start":140503923,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140503929,"alleles":["AAATAAA","AAA"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140503924,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503924,"clinical_significance":[],"id":"rs1201417636","seq_region_name":"7"},{"start":140503925,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140503924,"alleles":["-","GAAAAGAAAGAAAG"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795546669","clinical_significance":[]},{"seq_region_name":"7","id":"rs1247135419","clinical_significance":[],"start":140503926,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","-"],"end":140503926,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140503926,"alleles":["T","A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503926,"clinical_significance":[],"id":"rs1258618447","seq_region_name":"7"},{"start":140503926,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140503930,"alleles":["TAAAG","-"],"strand":1,"feature_type":"variation","id":"rs1795546758","seq_region_name":"7","clinical_significance":[]},{"start":140503929,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140503929,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1395097734","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503930,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140503930,"id":"rs1317672194","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585523545","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503931,"source":"dbSNP","strand":1,"feature_type":"variation","end":140503931,"alleles":["A","G","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs112461967","end":140503939,"alleles":["AAAAAAAAA","AAAAAAAA","AAAAAAAAAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140503931,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140503948,"alleles":["AAAAAAAAAGAACAAAAA","AAAAA"],"strand":1,"feature_type":"variation","start":140503931,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1193598985","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795546991","clinical_significance":[],"alleles":["A","G"],"end":140503934,"strand":1,"feature_type":"variation","start":140503934,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795547011","source":"dbSNP","start":140503935,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140503935,"alleles":["A","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795547037","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503936,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140503936},{"seq_region_name":"7","id":"rs1795547064","clinical_significance":[],"strand":1,"feature_type":"variation","end":140503941,"alleles":["AGA","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503939,"source":"dbSNP"},{"alleles":["G","A"],"end":140503940,"strand":1,"feature_type":"variation","start":140503940,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1423800021","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795547137","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","GG"],"end":140503940,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503940},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503940,"source":"dbSNP","strand":1,"feature_type":"variation","end":140503943,"alleles":["GAAC","-"],"seq_region_name":"7","id":"rs1186384437","clinical_significance":[]},{"id":"rs1478497878","seq_region_name":"7","clinical_significance":[],"start":140503941,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140503941,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs988372609","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503943,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140503943},{"clinical_significance":[],"seq_region_name":"7","id":"rs918152507","end":140503944,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140503944,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140503956,"alleles":["AAAAGAAAGAAA","AAAAGAAAGAAAAGAAAGAAA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503945,"source":"dbSNP","seq_region_name":"7","id":"rs1795547321","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503946,"source":"dbSNP","strand":1,"feature_type":"variation","end":140503957,"alleles":["AAAGAAAGAAAG","AAAGAAAG"],"id":"rs1348695340","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1399489406","feature_type":"variation","strand":1,"end":140503949,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503949},{"seq_region_name":"7","id":"rs1795547420","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503950,"source":"dbSNP","strand":1,"feature_type":"variation","end":140503950,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs1795547460","clinical_significance":[],"start":140503953,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140503953,"strand":1,"feature_type":"variation"},{"alleles":["-","T"],"end":140503953,"feature_type":"variation","strand":1,"source":"dbSNP","start":140503954,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795547481"},{"start":140503954,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AAAGTA","AAAGTAAAGTA"],"end":140503959,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795547508","clinical_significance":[]},{"alleles":["AAGTA","A"],"end":140503959,"strand":1,"feature_type":"variation","start":140503955,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1232442211","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503958,"source":"dbSNP","strand":1,"feature_type":"variation","end":140503958,"alleles":["T","A"],"seq_region_name":"7","id":"rs1563107309","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503959,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140503959,"clinical_significance":[],"id":"rs2130423283","seq_region_name":"7"},{"id":"rs1585523561","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140503963,"strand":1,"feature_type":"variation","start":140503963,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140503966,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140503966,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1466451744","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503969,"source":"dbSNP","strand":1,"feature_type":"variation","end":140503969,"alleles":["G","A","T"],"id":"rs1304377285","seq_region_name":"7","clinical_significance":[]},{"id":"rs1399721982","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503971,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140503971},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503972,"feature_type":"variation","strand":1,"end":140503972,"alleles":["T","C"],"clinical_significance":[],"id":"rs1795547741","seq_region_name":"7"},{"alleles":["T","G"],"end":140503975,"strand":1,"feature_type":"variation","start":140503975,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795547764","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795547795","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140503976,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503976},{"clinical_significance":[],"seq_region_name":"7","id":"rs1394570900","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503978,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140503978},{"clinical_significance":[],"seq_region_name":"7","id":"rs1324999360","source":"dbSNP","start":140503984,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["CC","CCCC"],"end":140503985,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503985,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140503985,"seq_region_name":"7","id":"rs949765389","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","-"],"end":140503987,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503987,"source":"dbSNP","seq_region_name":"7","id":"rs1312278840","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140503987,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140503987,"clinical_significance":[],"seq_region_name":"7","id":"rs1415861440"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1341256052","source":"dbSNP","start":140503992,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140503992,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1795548013","seq_region_name":"7","alleles":["A","G"],"end":140503995,"feature_type":"variation","strand":1,"source":"dbSNP","start":140503995,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","A"],"end":140503997,"feature_type":"variation","strand":1,"source":"dbSNP","start":140503997,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs529987731","seq_region_name":"7"},{"end":140503999,"alleles":["CAC","CACCAC"],"strand":1,"feature_type":"variation","start":140503997,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795548070","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140503998,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503998,"source":"dbSNP","seq_region_name":"7","id":"rs1795548096","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795548122","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140503999,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140503999,"source":"dbSNP"},{"end":140504009,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140504009,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1220523364"},{"clinical_significance":[],"id":"rs1795548185","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504010,"feature_type":"variation","strand":1,"alleles":["TGAGGTGAGTGGATCACTTGAGG","TGAGG"],"end":140504032},{"clinical_significance":[],"id":"rs1045366990","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140504013,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504013},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504014,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140504014,"clinical_significance":[],"id":"rs1168090714","seq_region_name":"7"},{"start":140504017,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140504017,"alleles":["A","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs79412100","clinical_significance":[]},{"id":"rs1585523597","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140504019,"alleles":["T","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504019,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563107329","alleles":["C","G","T"],"end":140504024,"feature_type":"variation","strand":1,"source":"dbSNP","start":140504024,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1317844124","seq_region_name":"7","clinical_significance":[],"start":140504026,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140504026,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504032,"feature_type":"variation","strand":1,"end":140504032,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs147894523"},{"source":"dbSNP","start":140504033,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140504033,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1048917888"},{"alleles":["G","A"],"end":140504036,"feature_type":"variation","strand":1,"source":"dbSNP","start":140504036,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1258194543"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504037,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140504037,"seq_region_name":"7","id":"rs1795548533","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140504038,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504038,"clinical_significance":[],"id":"rs910191582","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140504040,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504040,"source":"dbSNP","seq_region_name":"7","id":"rs1585523614","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1004782356","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504041,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140504041},{"seq_region_name":"7","id":"rs2130423380","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504049,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140504049},{"start":140504051,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140504051,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs947145460","seq_region_name":"7","clinical_significance":[]},{"start":140504052,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140504052,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs978561496","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795548674","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504054,"source":"dbSNP","strand":1,"feature_type":"variation","end":140504054,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs528008761","clinical_significance":[],"start":140504059,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140504059,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs924345736","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504061,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140504061},{"source":"dbSNP","start":140504067,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140504067,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795548718"},{"end":140504069,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140504069,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1269971764","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130423408","clinical_significance":[],"start":140504071,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140504071,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"end":140504073,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140504073,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs552472451","seq_region_name":"7"},{"id":"rs901731450","seq_region_name":"7","clinical_significance":[],"start":140504074,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140504074,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504075,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140504075,"clinical_significance":[],"seq_region_name":"7","id":"rs1795548802"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140504076,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504076,"source":"dbSNP","id":"rs1795548820","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795548836","clinical_significance":[],"start":140504086,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140504086,"strand":1,"feature_type":"variation"},{"id":"rs1294635571","seq_region_name":"7","clinical_significance":[],"alleles":["C","G"],"end":140504090,"strand":1,"feature_type":"variation","start":140504090,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795548868","clinical_significance":[],"start":140504100,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140504100,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs2130423427","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504102,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140504102},{"clinical_significance":[],"seq_region_name":"7","id":"rs12703959","alleles":["C","A","G"],"end":140504104,"feature_type":"variation","strand":1,"source":"dbSNP","start":140504104,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1412413523","feature_type":"variation","strand":1,"end":140504105,"alleles":["CC","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504104},{"source":"dbSNP","start":140504105,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140504105,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1411296484"},{"feature_type":"variation","strand":1,"end":140504106,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504106,"clinical_significance":[],"id":"rs538727980","seq_region_name":"7"},{"end":140504107,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140504107,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1169668228"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795549054","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504109,"feature_type":"variation","strand":1,"end":140504109,"alleles":["G","A"]},{"clinical_significance":[],"id":"rs1795549092","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","A"],"end":140504110,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504110},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130423461","source":"dbSNP","start":140504113,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140504113,"alleles":["T","A"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504114,"source":"dbSNP","strand":1,"feature_type":"variation","end":140504114,"alleles":["A","G","T"],"seq_region_name":"7","id":"rs1795549104","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130423467","feature_type":"variation","strand":1,"end":140504117,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504117},{"clinical_significance":[],"seq_region_name":"7","id":"rs1475518321","alleles":["G","A"],"end":140504122,"feature_type":"variation","strand":1,"source":"dbSNP","start":140504122,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs895742652","seq_region_name":"7","source":"dbSNP","start":140504126,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140504126,"alleles":["T","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795549153","end":140504127,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140504127,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1028956747","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504135,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140504135},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504137,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140504137,"clinical_significance":[],"id":"rs953627736","seq_region_name":"7"},{"start":140504138,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C","T"],"end":140504138,"strand":1,"feature_type":"variation","id":"rs557140724","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1000937444","clinical_significance":[],"alleles":["G","A"],"end":140504146,"strand":1,"feature_type":"variation","start":140504146,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795549232","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504149,"feature_type":"variation","strand":1,"end":140504149,"alleles":["G","A","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504150,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140504150,"seq_region_name":"7","id":"rs568977596","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795549288","clinical_significance":[],"strand":1,"feature_type":"variation","end":140504151,"alleles":["A","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504151,"source":"dbSNP"},{"start":140504152,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140504152,"strand":1,"feature_type":"variation","id":"rs1045107995","seq_region_name":"7","clinical_significance":[]},{"id":"rs143739380","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504159,"source":"dbSNP","strand":1,"feature_type":"variation","end":140504159,"alleles":["C","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504160,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140504160,"clinical_significance":[],"seq_region_name":"7","id":"rs1006622112"},{"alleles":["T","C"],"end":140504163,"feature_type":"variation","strand":1,"source":"dbSNP","start":140504163,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1465335033","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504164,"feature_type":"variation","strand":1,"end":140504164,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1233141702"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504166,"feature_type":"variation","strand":1,"end":140504166,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1312555632"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1361440838","source":"dbSNP","start":140504172,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140504172,"alleles":["G","C"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504178,"feature_type":"variation","strand":1,"end":140504178,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs58958884"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504181,"source":"dbSNP","strand":1,"feature_type":"variation","end":140504181,"alleles":["A","-"],"id":"rs1402004217","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130423508","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504181,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140504181},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795549475","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504182,"feature_type":"variation","strand":1,"end":140504182,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1016383537","clinical_significance":[],"strand":1,"feature_type":"variation","end":140504186,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504186,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1279621656","end":140504191,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140504191,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140504192,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504192,"clinical_significance":[],"seq_region_name":"7","id":"rs2130423518"},{"seq_region_name":"7","id":"rs1795549515","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504193,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140504193},{"clinical_significance":[],"seq_region_name":"7","id":"rs1443990258","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504201,"feature_type":"variation","strand":1,"end":140504204,"alleles":["CCCC","CCC"]},{"seq_region_name":"7","id":"rs897902986","clinical_significance":[],"strand":1,"feature_type":"variation","end":140504203,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504203,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504207,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140504207,"clinical_significance":[],"seq_region_name":"7","id":"rs1795549570"},{"clinical_significance":[],"seq_region_name":"7","id":"rs988279724","source":"dbSNP","start":140504209,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140504209,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1330221789","clinical_significance":[],"start":140504216,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140504216,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1296431343","feature_type":"variation","strand":1,"end":140504218,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504218},{"alleles":["G","A"],"end":140504221,"strand":1,"feature_type":"variation","start":140504221,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs2130423539","seq_region_name":"7","clinical_significance":[]},{"end":140504223,"alleles":["C","A","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140504223,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs541580707"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504224,"source":"dbSNP","strand":1,"feature_type":"variation","end":140504224,"alleles":["G","A"],"id":"rs183437239","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795549693","feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140504235,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504235},{"start":140504236,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140504236,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1304012792","clinical_significance":[]},{"seq_region_name":"7","id":"rs981552552","clinical_significance":[],"alleles":["T","C"],"end":140504237,"strand":1,"feature_type":"variation","start":140504237,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504239,"feature_type":"variation","strand":1,"end":140504241,"alleles":["TGT","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795549787"},{"seq_region_name":"7","id":"rs1408876498","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504244,"source":"dbSNP","strand":1,"feature_type":"variation","end":140504244,"alleles":["C","A"]},{"alleles":["A","AGA"],"end":140504245,"feature_type":"variation","strand":1,"source":"dbSNP","start":140504245,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1554454605"},{"start":140504245,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140504245,"alleles":["A","G"],"strand":1,"feature_type":"variation","id":"rs1585523706","seq_region_name":"7","clinical_significance":[]},{"alleles":["AAAAAAAAAAAA","AAAAAAAAAA","AAAAAAAAAAA","AAAAAAAAAAAAA","AAAAAAAAAAAAAA"],"end":140504256,"feature_type":"variation","strand":1,"source":"dbSNP","start":140504245,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs776319798"},{"start":140504246,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["-","G"],"end":140504245,"strand":1,"feature_type":"variation","id":"rs34633127","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs76083367","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504246,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140504246},{"alleles":["A","G"],"end":140504247,"feature_type":"variation","strand":1,"source":"dbSNP","start":140504247,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795550112"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504248,"feature_type":"variation","strand":1,"alleles":["A","C","G","T"],"end":140504248,"clinical_significance":[],"seq_region_name":"7","id":"rs1221557135"},{"alleles":["-","C"],"end":140504248,"feature_type":"variation","strand":1,"source":"dbSNP","start":140504249,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795550174"},{"alleles":["G","T"],"end":140504257,"feature_type":"variation","strand":1,"source":"dbSNP","start":140504257,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1318025898"},{"strand":1,"feature_type":"variation","end":140504258,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504258,"source":"dbSNP","seq_region_name":"7","id":"rs2130423600","clinical_significance":[]},{"source":"dbSNP","start":140504261,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140504261,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795550211"},{"id":"rs1287141749","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140504262,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504262,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["AAAAAA","AAA"],"end":140504267,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504262,"source":"dbSNP","id":"rs1284392391","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1347860831","clinical_significance":[],"start":140504263,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140504263,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504265,"feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140504265,"clinical_significance":[],"id":"rs34984111","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140504266,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504266,"source":"dbSNP","seq_region_name":"7","id":"rs1795550365","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504278,"feature_type":"variation","strand":1,"end":140504278,"alleles":["C","A"],"clinical_significance":[],"id":"rs375629506","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1372996683","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504281,"feature_type":"variation","strand":1,"alleles":["G","C","T"],"end":140504281},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504286,"source":"dbSNP","strand":1,"feature_type":"variation","end":140504289,"alleles":["CTAT","CTATCTAT"],"seq_region_name":"7","id":"rs1795550512","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1323624699","source":"dbSNP","start":140504287,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140504287,"alleles":["T","C"],"feature_type":"variation","strand":1},{"end":140504289,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140504289,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs141093977"},{"seq_region_name":"7","id":"rs1435729794","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504291,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140504291},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504292,"source":"dbSNP","strand":1,"feature_type":"variation","end":140504292,"alleles":["C","G","T"],"seq_region_name":"7","id":"rs1795550634","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795550666","feature_type":"variation","strand":1,"end":140504294,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504294},{"clinical_significance":[],"seq_region_name":"7","id":"rs1345677444","feature_type":"variation","strand":1,"end":140504300,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504300},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130423651","alleles":["A","G"],"end":140504301,"feature_type":"variation","strand":1,"source":"dbSNP","start":140504301,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs189035231","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504302,"source":"dbSNP","strand":1,"feature_type":"variation","end":140504302,"alleles":["T","G"]},{"source":"dbSNP","start":140504303,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140504303,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795550714"},{"seq_region_name":"7","id":"rs145189812","clinical_significance":[],"start":140504306,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140504306,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140504308,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504308,"source":"dbSNP","seq_region_name":"7","id":"rs954972911","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140504312,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504312,"clinical_significance":[],"id":"rs908944519","seq_region_name":"7"},{"seq_region_name":"7","id":"rs986325052","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140504316,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504316,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795550817","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140504317,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504317,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1018256819","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504318,"feature_type":"variation","strand":1,"end":140504318,"alleles":["A","G"]},{"clinical_significance":[],"id":"rs1795550861","seq_region_name":"7","source":"dbSNP","start":140504325,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140504325,"alleles":["A","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795550884","clinical_significance":[],"start":140504326,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140504326,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1795550898","clinical_significance":[],"alleles":["C","G"],"end":140504335,"strand":1,"feature_type":"variation","start":140504335,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140504336,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140504336,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs2885918","seq_region_name":"7"},{"start":140504337,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140504337,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs544002132","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504340,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140504340,"id":"rs1585523786","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1469464374","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504341,"feature_type":"variation","strand":1,"end":140504341,"alleles":["C","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1455738269","source":"dbSNP","start":140504342,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140504342,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1795551057","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504344,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140504344},{"seq_region_name":"7","id":"rs2130423698","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504351,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TT","T"],"end":140504352},{"clinical_significance":[],"id":"rs2363818","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504352,"feature_type":"variation","strand":1,"alleles":["T","A","C","G"],"end":140504352},{"seq_region_name":"7","id":"rs2130423711","clinical_significance":[],"alleles":["T","A"],"end":140504355,"strand":1,"feature_type":"variation","start":140504355,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs2130423713","clinical_significance":[],"start":140504355,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","-"],"end":140504355,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs759246627","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504356,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140504356},{"clinical_significance":[],"id":"rs752305582","seq_region_name":"7","end":140504364,"alleles":["TTTTTTTT","TTTTTTT","TTTTTTTTT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140504357,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140504358,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504358,"source":"dbSNP","seq_region_name":"7","id":"rs924386099","clinical_significance":[]},{"end":140504364,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140504364,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795551223"},{"clinical_significance":[],"id":"rs1159027182","seq_region_name":"7","alleles":["A","G"],"end":140504368,"feature_type":"variation","strand":1,"source":"dbSNP","start":140504368,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140504369,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504369,"clinical_significance":[],"seq_region_name":"7","id":"rs1795551254"},{"clinical_significance":[],"id":"rs1284680044","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504371,"feature_type":"variation","strand":1,"end":140504371,"alleles":["T","C"]},{"source":"dbSNP","start":140504372,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140504372,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs574578503"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504378,"source":"dbSNP","strand":1,"feature_type":"variation","end":140504378,"alleles":["A","G"],"id":"rs1795551332","seq_region_name":"7","clinical_significance":[]},{"start":140504379,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140504379,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs767350320","clinical_significance":[]},{"start":140504387,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140504387,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795551374","clinical_significance":[]},{"start":140504391,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140504391,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795551396","clinical_significance":[]},{"id":"rs1795551413","seq_region_name":"7","clinical_significance":[],"alleles":["A","G"],"end":140504394,"strand":1,"feature_type":"variation","start":140504394,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1795551432","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140504396,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504396},{"seq_region_name":"7","id":"rs1000844563","clinical_significance":[],"strand":1,"feature_type":"variation","end":140504401,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504401,"source":"dbSNP"},{"start":140504402,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140504402,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1362333965","clinical_significance":[]},{"seq_region_name":"7","id":"rs1290569718","clinical_significance":[],"start":140504403,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140504403,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1428551922","clinical_significance":[],"alleles":["C","T"],"end":140504405,"strand":1,"feature_type":"variation","start":140504405,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140504407,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140504407,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs541887372","seq_region_name":"7"},{"id":"rs1313537290","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140504413,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504413,"source":"dbSNP"},{"start":140504415,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140504415,"alleles":["A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795551577","clinical_significance":[]},{"seq_region_name":"7","id":"rs1157072853","clinical_significance":[],"alleles":["C","T"],"end":140504417,"strand":1,"feature_type":"variation","start":140504417,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795551603","feature_type":"variation","strand":1,"end":140504434,"alleles":["AGGGAGACGGATTTGAG","AG"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504418},{"clinical_significance":[],"id":"rs1436862869","seq_region_name":"7","source":"dbSNP","start":140504421,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140504421,"feature_type":"variation","strand":1},{"alleles":["G","C"],"end":140504423,"feature_type":"variation","strand":1,"source":"dbSNP","start":140504423,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1032441105"},{"seq_region_name":"7","id":"rs560511571","clinical_significance":[],"alleles":["C","A","T"],"end":140504425,"strand":1,"feature_type":"variation","start":140504425,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs796262251","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140504426,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504426},{"seq_region_name":"7","id":"rs1795551717","clinical_significance":[],"strand":1,"feature_type":"variation","end":140504427,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504427,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1009739213","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504432,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140504432},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504438,"feature_type":"variation","strand":1,"end":140504438,"alleles":["G","A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs531295617"},{"end":140504441,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140504441,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1488241503","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1366152764","feature_type":"variation","strand":1,"end":140504442,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504442},{"seq_region_name":"7","id":"rs1795551852","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504448,"source":"dbSNP","strand":1,"feature_type":"variation","end":140504448,"alleles":["C","A"]},{"end":140504450,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140504450,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1210937424","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504453,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140504453,"clinical_significance":[],"seq_region_name":"7","id":"rs1795551902"},{"start":140504453,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140504455,"alleles":["GGG","GG"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1253900598","clinical_significance":[]},{"seq_region_name":"7","id":"rs948516393","clinical_significance":[],"strand":1,"feature_type":"variation","end":140504456,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504456,"source":"dbSNP"},{"end":140504459,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140504459,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795551976"},{"start":140504461,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140504461,"strand":1,"feature_type":"variation","id":"rs1307931843","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs971418955","clinical_significance":[],"alleles":["A","C"],"end":140504463,"strand":1,"feature_type":"variation","start":140504463,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795552034","clinical_significance":[],"start":140504463,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140504476,"alleles":["ACCCCTTGTACCCC","ACCCC"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504464,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140504464,"seq_region_name":"7","id":"rs1044362117","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504465,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140504465,"clinical_significance":[],"seq_region_name":"7","id":"rs1795552069"},{"source":"dbSNP","start":140504466,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140504466,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs549908267","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795552130","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504468,"source":"dbSNP","strand":1,"feature_type":"variation","end":140504468,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs926977177","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504468,"feature_type":"variation","strand":1,"end":140504469,"alleles":["TT","T","TTT"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs552796064","feature_type":"variation","strand":1,"end":140504469,"alleles":["T","C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504469},{"alleles":["CCCCCC","CCCCC"],"end":140504478,"strand":1,"feature_type":"variation","start":140504473,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795552239","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs958386036","alleles":["C","G","T"],"end":140504474,"feature_type":"variation","strand":1,"source":"dbSNP","start":140504474,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795552318","feature_type":"variation","strand":1,"end":140504475,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504475},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563107441","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140504476,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504476},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504477,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140504477,"seq_region_name":"7","id":"rs1795552397","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504478,"feature_type":"variation","strand":1,"end":140504478,"alleles":["C","A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs2363819"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504480,"feature_type":"variation","strand":1,"end":140504480,"alleles":["C","A"],"clinical_significance":[],"id":"rs1795552551","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795552574","feature_type":"variation","strand":1,"end":140504482,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504482},{"seq_region_name":"7","id":"rs1795552602","clinical_significance":[],"start":140504487,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140504487,"strand":1,"feature_type":"variation"},{"alleles":["C","T"],"end":140504489,"feature_type":"variation","strand":1,"source":"dbSNP","start":140504489,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795552628"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504491,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140504491,"seq_region_name":"7","id":"rs1795552660","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs942082238","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140504494,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504494},{"seq_region_name":"7","id":"rs1168747800","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504499,"source":"dbSNP","strand":1,"feature_type":"variation","end":140504507,"alleles":["CTTCTTCTT","CTTCTT"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs142373515","source":"dbSNP","start":140504514,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","AA"],"end":140504514,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140504518,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140504518,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795552861"},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140504521,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504521,"clinical_significance":[],"id":"rs1038068187","seq_region_name":"7"},{"start":140504522,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140504522,"alleles":["T","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs940405318","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795552944","clinical_significance":[],"alleles":["G","A"],"end":140504527,"strand":1,"feature_type":"variation","start":140504527,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs2130423871","clinical_significance":[],"alleles":["T","C"],"end":140504529,"strand":1,"feature_type":"variation","start":140504529,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs115295972","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504532,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140504532},{"clinical_significance":[],"id":"rs1223163666","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140504533,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504533},{"clinical_significance":[],"id":"rs1795553055","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504537,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140504537},{"start":140504542,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140504542,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs115682570","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1180985745","seq_region_name":"7","feature_type":"variation","strand":1,"end":140504543,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504543},{"end":140504544,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140504544,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795553087"},{"seq_region_name":"7","id":"rs2130423881","clinical_significance":[],"end":140504548,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140504548,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140504549,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504549,"source":"dbSNP","seq_region_name":"7","id":"rs1795553108","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140504552,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504552,"source":"dbSNP","seq_region_name":"7","id":"rs1488122409","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140504553,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504553,"clinical_significance":[],"id":"rs2130423889","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130423891","alleles":["T","C"],"end":140504560,"feature_type":"variation","strand":1,"source":"dbSNP","start":140504560,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140504563,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504563,"source":"dbSNP","seq_region_name":"7","id":"rs1480743908","clinical_significance":[]},{"alleles":["A","C"],"end":140504565,"feature_type":"variation","strand":1,"source":"dbSNP","start":140504565,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585523900"},{"alleles":["C","A"],"end":140504567,"feature_type":"variation","strand":1,"source":"dbSNP","start":140504567,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1563107468"},{"feature_type":"variation","strand":1,"end":140504571,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504571,"clinical_significance":[],"seq_region_name":"7","id":"rs1252898890"},{"clinical_significance":[],"seq_region_name":"7","id":"rs933256212","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140504576,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504576},{"clinical_significance":[],"id":"rs1179162336","seq_region_name":"7","feature_type":"variation","strand":1,"end":140504580,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504580},{"alleles":["A","G"],"end":140504582,"strand":1,"feature_type":"variation","start":140504582,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130423908","clinical_significance":[]},{"end":140504585,"alleles":["GG","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140504584,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795553285"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504590,"source":"dbSNP","strand":1,"feature_type":"variation","end":140504590,"alleles":["G","T"],"seq_region_name":"7","id":"rs1795553305","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504592,"feature_type":"variation","strand":1,"end":140504592,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795553331"},{"strand":1,"feature_type":"variation","alleles":["C","A","G","T"],"end":140504596,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504596,"source":"dbSNP","seq_region_name":"7","id":"rs1030477816","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795553446","end":140504600,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140504600,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1437555854","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504601,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140504601},{"start":140504603,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140504603,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs1795553503","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1234989197","seq_region_name":"7","end":140504605,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140504605,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs756813515","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504606,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140504606},{"seq_region_name":"7","id":"rs1407558981","clinical_significance":[],"alleles":["C","A"],"end":140504611,"strand":1,"feature_type":"variation","start":140504611,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs192092544","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140504617,"strand":1,"feature_type":"variation","start":140504617,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs536320740","seq_region_name":"7","alleles":["A","C"],"end":140504623,"feature_type":"variation","strand":1,"source":"dbSNP","start":140504623,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["A","G","T"],"end":140504626,"feature_type":"variation","strand":1,"source":"dbSNP","start":140504626,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1296623027","seq_region_name":"7"},{"seq_region_name":"7","id":"rs750940275","clinical_significance":[],"alleles":["T","C"],"end":140504627,"strand":1,"feature_type":"variation","start":140504627,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140504629,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140504629,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1395596232","clinical_significance":[]},{"start":140504630,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140504630,"strand":1,"feature_type":"variation","id":"rs1795553839","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1167826626","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504630,"source":"dbSNP","strand":1,"feature_type":"variation","end":140504634,"alleles":["AAAAA","AAAA"]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140504634,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504634,"clinical_significance":[],"id":"rs1053745957","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1795553906","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504636,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140504636},{"seq_region_name":"7","id":"rs1366260496","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140504639,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504639,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1167007317","clinical_significance":[],"strand":1,"feature_type":"variation","end":140504640,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504640,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504641,"source":"dbSNP","strand":1,"feature_type":"variation","end":140504641,"alleles":["G","A"],"seq_region_name":"7","id":"rs1419111437","clinical_significance":[]},{"id":"rs1795554074","seq_region_name":"7","clinical_significance":[],"end":140504648,"alleles":["GGGCGTGG","GG"],"strand":1,"feature_type":"variation","start":140504641,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140504644,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504644,"source":"dbSNP","seq_region_name":"7","id":"rs969335253","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs547896314","alleles":["G","A","T"],"end":140504645,"feature_type":"variation","strand":1,"source":"dbSNP","start":140504645,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140504650,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140504650,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795554189","clinical_significance":[]},{"id":"rs1795554209","seq_region_name":"7","clinical_significance":[],"end":140504651,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140504651,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504652,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140504652,"clinical_significance":[],"seq_region_name":"7","id":"rs2130423969"},{"end":140504653,"alleles":["CA","-"],"strand":1,"feature_type":"variation","start":140504652,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1332627352","clinical_significance":[]},{"clinical_significance":[],"id":"rs566426450","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504654,"feature_type":"variation","strand":1,"end":140504654,"alleles":["T","C","G"]},{"alleles":["A","G"],"end":140504655,"strand":1,"feature_type":"variation","start":140504655,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795554273","clinical_significance":[]},{"id":"rs182758606","seq_region_name":"7","clinical_significance":[],"start":140504656,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140504656,"strand":1,"feature_type":"variation"},{"alleles":["-","AT"],"end":140504656,"strand":1,"feature_type":"variation","start":140504657,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795554338","clinical_significance":[]},{"id":"rs558861700","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504657,"source":"dbSNP","strand":1,"feature_type":"variation","end":140504657,"alleles":["G","A"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504657,"feature_type":"variation","strand":1,"alleles":["G","GTG"],"end":140504657,"clinical_significance":[],"id":"rs1795554401","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795554451","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140504659,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504659},{"strand":1,"feature_type":"variation","end":140504660,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504660,"source":"dbSNP","seq_region_name":"7","id":"rs1795554494","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504661,"feature_type":"variation","strand":1,"end":140504661,"alleles":["G","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795554528"},{"alleles":["T","A","G"],"end":140504664,"feature_type":"variation","strand":1,"source":"dbSNP","start":140504664,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs955791953","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585523962","end":140504668,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140504668,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504669,"feature_type":"variation","strand":1,"end":140504669,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs992600259"},{"seq_region_name":"7","id":"rs1795554628","clinical_significance":[],"alleles":["C","G"],"end":140504671,"strand":1,"feature_type":"variation","start":140504671,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140504673,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140504673,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795554650","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504674,"source":"dbSNP","strand":1,"feature_type":"variation","end":140504674,"alleles":["C","T"],"seq_region_name":"7","id":"rs1795554683","clinical_significance":[]},{"source":"dbSNP","start":140504676,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140504676,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs916989126"},{"id":"rs1379486919","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140504677,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504677,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795554789","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140504678,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504678},{"id":"rs969913275","seq_region_name":"7","clinical_significance":[],"alleles":["G","T"],"end":140504679,"strand":1,"feature_type":"variation","start":140504679,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504685,"feature_type":"variation","strand":1,"end":140504685,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585523973"},{"seq_region_name":"7","id":"rs1307361939","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504688,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140504688},{"clinical_significance":[],"seq_region_name":"7","id":"rs1229616282","feature_type":"variation","strand":1,"end":140504689,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504689},{"id":"rs980340653","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504690,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140504690},{"id":"rs1310024129","seq_region_name":"7","clinical_significance":[],"end":140504692,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140504692,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140504699,"alleles":["A","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504699,"source":"dbSNP","seq_region_name":"7","id":"rs1333514313","clinical_significance":[]},{"id":"rs1795555044","seq_region_name":"7","clinical_significance":[],"start":140504699,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["ACT","-"],"end":140504701,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1385637316","clinical_significance":[],"end":140504700,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140504700,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140504706,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140504706,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1390687823"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130424045","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140504707,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504707},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140504708,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504708,"source":"dbSNP","id":"rs909803108","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795555146","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504709,"feature_type":"variation","strand":1,"end":140504709,"alleles":["G","A","C"]},{"alleles":["G","T"],"end":140504710,"strand":1,"feature_type":"variation","start":140504710,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130424048","clinical_significance":[]},{"source":"dbSNP","start":140504711,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140504711,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs941241737","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795555211","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504714,"feature_type":"variation","strand":1,"end":140504714,"alleles":["G","A"]},{"clinical_significance":[],"id":"rs576718368","seq_region_name":"7","source":"dbSNP","start":140504715,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140504715,"alleles":["C","T"],"feature_type":"variation","strand":1},{"start":140504716,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140504716,"strand":1,"feature_type":"variation","id":"rs1037721551","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504720,"feature_type":"variation","strand":1,"end":140504720,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs537685127"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140504721,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504721,"clinical_significance":[],"seq_region_name":"7","id":"rs1668861033"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1237769028","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140504722,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504722},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795555389","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504723,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140504723},{"seq_region_name":"7","id":"rs1795555420","clinical_significance":[],"strand":1,"feature_type":"variation","end":140504728,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504728,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795555459","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504730,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140504730},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504731,"feature_type":"variation","strand":1,"end":140504731,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795555487"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504732,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140504732,"clinical_significance":[],"seq_region_name":"7","id":"rs929291908"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1183803799","end":140504733,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140504733,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504734,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140504734,"clinical_significance":[],"id":"rs1051828249","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140504736,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504736,"source":"dbSNP","seq_region_name":"7","id":"rs1795555648","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140504738,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504738,"source":"dbSNP","seq_region_name":"7","id":"rs1266610800","clinical_significance":[]},{"seq_region_name":"7","id":"rs758629579","clinical_significance":[],"end":140504739,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140504739,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1172080660","clinical_significance":[],"strand":1,"feature_type":"variation","end":140504740,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504740,"source":"dbSNP"},{"end":140504741,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140504741,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1007682648","clinical_significance":[]},{"id":"rs1403118346","seq_region_name":"7","clinical_significance":[],"start":140504742,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140504742,"alleles":["C","G","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1464487740","clinical_significance":[],"start":140504745,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140504745,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795555886","end":140504746,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140504746,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140504747,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504747,"clinical_significance":[],"seq_region_name":"7","id":"rs1795555910"},{"clinical_significance":[],"id":"rs1231560059","seq_region_name":"7","feature_type":"variation","strand":1,"end":140504748,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504748},{"source":"dbSNP","start":140504749,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140504749,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585524024"},{"id":"rs1039576894","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504750,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140504750},{"seq_region_name":"7","id":"rs1795556004","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504753,"source":"dbSNP","strand":1,"feature_type":"variation","end":140504753,"alleles":["C","T"]},{"start":140504754,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140504754,"strand":1,"feature_type":"variation","id":"rs904785192","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","A","T"],"end":140504755,"feature_type":"variation","strand":1,"source":"dbSNP","start":140504755,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs370737513"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140504757,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504757,"source":"dbSNP","seq_region_name":"7","id":"rs1319565469","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504759,"source":"dbSNP","strand":1,"feature_type":"variation","end":140504759,"alleles":["G","A"],"seq_region_name":"7","id":"rs1384416256","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140504761,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504761,"source":"dbSNP","seq_region_name":"7","id":"rs1795556126","clinical_significance":[]},{"start":140504762,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140504762,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs137873265","clinical_significance":[]},{"alleles":["G","A"],"end":140504763,"strand":1,"feature_type":"variation","start":140504763,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795556202","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140504765,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504765,"clinical_significance":[],"seq_region_name":"7","id":"rs1015878530"},{"alleles":["G","A"],"end":140504769,"feature_type":"variation","strand":1,"source":"dbSNP","start":140504769,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs955719407"},{"alleles":["G","A"],"end":140504775,"feature_type":"variation","strand":1,"source":"dbSNP","start":140504775,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs751353514"},{"seq_region_name":"7","id":"rs1013920700","clinical_significance":[],"start":140504780,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140504780,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1173916456","seq_region_name":"7","alleles":["C","T"],"end":140504783,"feature_type":"variation","strand":1,"source":"dbSNP","start":140504783,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504784,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140504784,"seq_region_name":"7","id":"rs1795556359","clinical_significance":[]},{"clinical_significance":[],"id":"rs2130424135","seq_region_name":"7","source":"dbSNP","start":140504786,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140504786,"feature_type":"variation","strand":1},{"end":140504787,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140504787,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795556385","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140504808,"alleles":["AAATAAATAAATAAATAAA","AAATAAATAAATAAA","AAATAAATAAATAAATAAATAAA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504790,"clinical_significance":[],"id":"rs1476924323","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1024099848","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504795,"source":"dbSNP","strand":1,"feature_type":"variation","end":140504795,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs778552310","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504802,"feature_type":"variation","strand":1,"alleles":["AAA","AAAA"],"end":140504804},{"source":"dbSNP","start":140504804,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140504804,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795556532"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504810,"feature_type":"variation","strand":1,"end":140504810,"alleles":["T","C"],"clinical_significance":[],"id":"rs574615414","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1261179949","clinical_significance":[],"strand":1,"feature_type":"variation","end":140504816,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504816,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504817,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140504817,"clinical_significance":[],"seq_region_name":"7","id":"rs780486720"},{"clinical_significance":[],"id":"rs909692644","seq_region_name":"7","end":140504820,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140504820,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs962680845","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504821,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140504821},{"id":"rs933179958","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504822,"source":"dbSNP","strand":1,"feature_type":"variation","end":140504822,"alleles":["G","A"]},{"alleles":["G","A"],"end":140504823,"feature_type":"variation","strand":1,"source":"dbSNP","start":140504823,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1198878440"},{"seq_region_name":"7","id":"rs747157179","clinical_significance":[],"alleles":["C","T"],"end":140504824,"strand":1,"feature_type":"variation","start":140504824,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504825,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140504825,"clinical_significance":[],"seq_region_name":"7","id":"rs142384769"},{"seq_region_name":"7","id":"rs1795556867","clinical_significance":[],"end":140504828,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140504828,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140504829,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504829,"clinical_significance":[],"id":"rs1795556896","seq_region_name":"7"},{"alleles":["G","A"],"end":140504830,"feature_type":"variation","strand":1,"source":"dbSNP","start":140504830,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795556921"},{"id":"rs918472835","seq_region_name":"7","clinical_significance":[],"start":140504831,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140504831,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["C","A","G","T"],"end":140504836,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504836,"clinical_significance":[],"seq_region_name":"7","id":"rs1443926895"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140504837,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504837,"clinical_significance":[],"id":"rs929314601","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795557006","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504841,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140504841},{"seq_region_name":"7","id":"rs1585524063","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504851,"source":"dbSNP","strand":1,"feature_type":"variation","end":140504851,"alleles":["C","T"]},{"start":140504852,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140504852,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795557045","clinical_significance":[]},{"clinical_significance":[],"id":"rs2130424184","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140504859,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504859},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795557060","feature_type":"variation","strand":1,"end":140504861,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504861},{"start":140504864,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140504864,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1051715709","clinical_significance":[]},{"seq_region_name":"7","id":"rs936567253","clinical_significance":[],"strand":1,"feature_type":"variation","end":140504865,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504865,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140504869,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504869,"source":"dbSNP","id":"rs1375456736","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504870,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140504870,"seq_region_name":"7","id":"rs912013562","clinical_significance":[]},{"seq_region_name":"7","id":"rs943437201","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504871,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140504871},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140504872,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504872,"source":"dbSNP","seq_region_name":"7","id":"rs1401296244","clinical_significance":[]},{"clinical_significance":[],"id":"rs1168253216","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140504873,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504873},{"alleles":["C","A"],"end":140504878,"feature_type":"variation","strand":1,"source":"dbSNP","start":140504878,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795557236"},{"feature_type":"variation","strand":1,"end":140504880,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504880,"clinical_significance":[],"seq_region_name":"7","id":"rs1466958660"},{"alleles":["C","A"],"end":140504881,"feature_type":"variation","strand":1,"source":"dbSNP","start":140504881,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs144611345"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504882,"feature_type":"variation","strand":1,"alleles":["TGATG","TG"],"end":140504886,"clinical_significance":[],"seq_region_name":"7","id":"rs1192779825"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504885,"feature_type":"variation","strand":1,"end":140504885,"alleles":["T","A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795557298"},{"strand":1,"feature_type":"variation","end":140504886,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504886,"source":"dbSNP","seq_region_name":"7","id":"rs1425787866","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795557354","source":"dbSNP","start":140504890,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140504890,"alleles":["G","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1259700143","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504894,"source":"dbSNP","strand":1,"feature_type":"variation","end":140504894,"alleles":["T","C","G"]},{"source":"dbSNP","start":140504896,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140504896,"alleles":["T","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs904709195"},{"clinical_significance":[],"id":"rs1442035451","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504897,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140504897},{"strand":1,"feature_type":"variation","end":140504899,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504899,"source":"dbSNP","id":"rs1795557437","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795557454","alleles":["C","A"],"end":140504901,"feature_type":"variation","strand":1,"source":"dbSNP","start":140504901,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795557482","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504909,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140504909},{"end":140504915,"alleles":["A","AA"],"strand":1,"feature_type":"variation","start":140504915,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795557502","clinical_significance":[]},{"start":140504918,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140504918,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1274195867","clinical_significance":[]},{"source":"dbSNP","start":140504924,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["CCC","CC"],"end":140504926,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795557548"},{"seq_region_name":"7","id":"rs1197958507","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140504927,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504927,"source":"dbSNP"},{"start":140504931,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140504931,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1316395123","clinical_significance":[]},{"start":140504934,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140504934,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1000341240","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs565712711","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140504939,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504939},{"alleles":["A","T"],"end":140504940,"strand":1,"feature_type":"variation","start":140504940,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795557639","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795557656","clinical_significance":[],"alleles":["AAAAAA","AAAAA"],"end":140504950,"strand":1,"feature_type":"variation","start":140504945,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["A","G"],"end":140504950,"strand":1,"feature_type":"variation","start":140504950,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1234363671","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795557722","clinical_significance":[],"start":140504953,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140504953,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140504957,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140504957,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1355612816","seq_region_name":"7"},{"clinical_significance":[],"id":"rs892013487","seq_region_name":"7","source":"dbSNP","start":140504960,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140504960,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504961,"source":"dbSNP","strand":1,"feature_type":"variation","end":140504961,"alleles":["A","G","T"],"seq_region_name":"7","id":"rs10279867","clinical_significance":[]},{"seq_region_name":"7","id":"rs1329064427","clinical_significance":[],"strand":1,"feature_type":"variation","end":140504962,"alleles":["T","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504962,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1795557911","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504966,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140504966},{"id":"rs1585524124","seq_region_name":"7","clinical_significance":[],"start":140504968,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140504968,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140504970,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504970,"source":"dbSNP","seq_region_name":"7","id":"rs1467007504","clinical_significance":[]},{"seq_region_name":"7","id":"rs1397766135","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504971,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140504971},{"start":140504972,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140504972,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795557973","clinical_significance":[]},{"seq_region_name":"7","id":"rs1169967256","clinical_significance":[],"strand":1,"feature_type":"variation","end":140504973,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504973,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140504977,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504977,"source":"dbSNP","seq_region_name":"7","id":"rs1461883390","clinical_significance":[]},{"clinical_significance":[],"id":"rs781079810","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140504979,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504979},{"clinical_significance":[],"seq_region_name":"7","id":"rs1416494614","feature_type":"variation","strand":1,"end":140504987,"alleles":["A","C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504987},{"clinical_significance":[],"seq_region_name":"7","id":"rs1161502103","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504988,"feature_type":"variation","strand":1,"end":140504988,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1472485781","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504990,"feature_type":"variation","strand":1,"end":140504990,"alleles":["C","T"]},{"clinical_significance":[],"id":"rs1233689202","seq_region_name":"7","feature_type":"variation","strand":1,"end":140504992,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504992},{"seq_region_name":"7","id":"rs1180676793","clinical_significance":[],"alleles":["G","A"],"end":140504993,"strand":1,"feature_type":"variation","start":140504993,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1002386538","clinical_significance":[],"start":140504994,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140504994,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140504995,"feature_type":"variation","strand":1,"end":140504995,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795558162"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140504998,"source":"dbSNP","strand":1,"feature_type":"variation","end":140504998,"alleles":["C","G"],"seq_region_name":"7","id":"rs1237946959","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs368885363","alleles":["C","T"],"end":140504999,"feature_type":"variation","strand":1,"source":"dbSNP","start":140504999,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505000,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140505000,"clinical_significance":[],"seq_region_name":"7","id":"rs1795558274"},{"end":140505002,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140505002,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795558308","clinical_significance":[]},{"clinical_significance":[],"id":"rs149271675","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505005,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140505005},{"seq_region_name":"7","id":"rs1288307820","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505006,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140505006},{"source":"dbSNP","start":140505008,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140505008,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1226143488"},{"strand":1,"feature_type":"variation","end":140505010,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505010,"source":"dbSNP","seq_region_name":"7","id":"rs1354973897","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140505014,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505014,"clinical_significance":[],"seq_region_name":"7","id":"rs1795558459"},{"clinical_significance":[],"seq_region_name":"7","id":"rs750325123","feature_type":"variation","strand":1,"end":140505015,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505015},{"clinical_significance":[],"id":"rs1448529711","seq_region_name":"7","source":"dbSNP","start":140505019,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140505019,"alleles":["G","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795558557","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505022,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140505022},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795558582","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505023,"feature_type":"variation","strand":1,"end":140505023,"alleles":["C","T"]},{"id":"rs186891455","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140505025,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505025,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1585524169","clinical_significance":[],"start":140505031,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140505031,"alleles":["T","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1330402295","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505035,"feature_type":"variation","strand":1,"end":140505035,"alleles":["G","A"]},{"start":140505036,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140505036,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1337758155","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585524179","clinical_significance":[],"alleles":["T","C","G"],"end":140505037,"strand":1,"feature_type":"variation","start":140505037,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1001672536","seq_region_name":"7","feature_type":"variation","strand":1,"end":140505040,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505040},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505044,"feature_type":"variation","strand":1,"end":140505044,"alleles":["G","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1351575749"},{"id":"rs1795558825","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505047,"source":"dbSNP","strand":1,"feature_type":"variation","end":140505047,"alleles":["C","A"]},{"strand":1,"feature_type":"variation","end":140505048,"alleles":["T","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505048,"source":"dbSNP","seq_region_name":"7","id":"rs10224830","clinical_significance":[]},{"alleles":["G","A","C"],"end":140505049,"feature_type":"variation","strand":1,"source":"dbSNP","start":140505049,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1016658490","seq_region_name":"7"},{"start":140505054,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","T"],"end":140505054,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1408720932","clinical_significance":[]},{"id":"rs1217289942","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505055,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140505055},{"seq_region_name":"7","id":"rs1279295958","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505056,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140505056},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505057,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140505057,"id":"rs1563107602","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1015913129","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140505060,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505060,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795559216","clinical_significance":[],"strand":1,"feature_type":"variation","end":140505061,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505061,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140505064,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505064,"source":"dbSNP","seq_region_name":"7","id":"rs1795559242","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1380126868","end":140505065,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140505065,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505072,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140505072,"clinical_significance":[],"id":"rs1194690395","seq_region_name":"7"},{"start":140505081,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140505081,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585524198","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505086,"feature_type":"variation","strand":1,"end":140505086,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1489645041"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1245501189","alleles":["C","A"],"end":140505087,"feature_type":"variation","strand":1,"source":"dbSNP","start":140505087,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1221396618","clinical_significance":[],"strand":1,"feature_type":"variation","end":140505088,"alleles":["A","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505088,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505091,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140505091,"clinical_significance":[],"seq_region_name":"7","id":"rs1347438289"},{"feature_type":"variation","strand":1,"alleles":["G","-"],"end":140505092,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505092,"clinical_significance":[],"seq_region_name":"7","id":"rs1284331811"},{"source":"dbSNP","start":140505092,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140505092,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795559439"},{"source":"dbSNP","start":140505094,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140505094,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1353550082"},{"seq_region_name":"7","id":"rs1795559528","clinical_significance":[],"end":140505097,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140505097,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795559558","clinical_significance":[],"strand":1,"feature_type":"variation","end":140505100,"alleles":["TCTC","TC"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505097,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["T","-"],"end":140505099,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505099,"source":"dbSNP","seq_region_name":"7","id":"rs1563107631","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs747592263","feature_type":"variation","strand":1,"end":140505100,"alleles":["C","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505100},{"clinical_significance":[],"id":"rs1351013926","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140505100,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505100},{"seq_region_name":"7","id":"rs1554454711","clinical_significance":[],"alleles":["CA","-"],"end":140505101,"strand":1,"feature_type":"variation","start":140505100,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585524215","feature_type":"variation","strand":1,"end":140505101,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505101},{"clinical_significance":[],"seq_region_name":"7","id":"rs34344129","source":"dbSNP","start":140505101,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AAAAAAAAAAAAAAAAAA","AAAAAAAAAA","AAAAAAAAAAAAAA","AAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAA"],"end":140505118,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140505103,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505103,"clinical_significance":[],"seq_region_name":"7","id":"rs962873920"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140505110,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505110,"clinical_significance":[],"seq_region_name":"7","id":"rs1795559997"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795560021","feature_type":"variation","strand":1,"end":140505111,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505111},{"clinical_significance":[],"seq_region_name":"7","id":"rs972556329","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505118,"feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140505118},{"seq_region_name":"7","id":"rs1217601591","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["AT","-"],"end":140505119,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505118,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1265510386","end":140505119,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140505119,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1445321063","clinical_significance":[],"end":140505120,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140505120,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795560154","clinical_significance":[],"alleles":["TT","T"],"end":140505122,"strand":1,"feature_type":"variation","start":140505121,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs576036402","feature_type":"variation","strand":1,"end":140505123,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505123},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795560206","source":"dbSNP","start":140505123,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140505126,"alleles":["CCCC","CCC"],"feature_type":"variation","strand":1},{"alleles":["A","C","G"],"end":140505127,"feature_type":"variation","strand":1,"source":"dbSNP","start":140505127,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585524247"},{"start":140505133,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140505133,"alleles":["T","G"],"strand":1,"feature_type":"variation","id":"rs1056990201","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795560271","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140505140,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505140,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140505141,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505141,"source":"dbSNP","seq_region_name":"7","id":"rs544302388","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140505145,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505145,"clinical_significance":[],"id":"rs955286215","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1247823852","clinical_significance":[],"start":140505150,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140505150,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140505155,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505155,"clinical_significance":[],"seq_region_name":"7","id":"rs1174438383"},{"strand":1,"feature_type":"variation","end":140505157,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505157,"source":"dbSNP","seq_region_name":"7","id":"rs1795560356","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140505161,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505161,"clinical_significance":[],"seq_region_name":"7","id":"rs1795560372"},{"end":140505163,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140505163,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795560400"},{"seq_region_name":"7","id":"rs1795560414","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505165,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140505165},{"seq_region_name":"7","id":"rs543364615","clinical_significance":[],"start":140505178,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140505178,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505180,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140505180,"clinical_significance":[],"seq_region_name":"7","id":"rs1795560463"},{"id":"rs1423499871","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505181,"source":"dbSNP","strand":1,"feature_type":"variation","end":140505181,"alleles":["G","T"]},{"source":"dbSNP","start":140505183,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140505183,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs911876210"},{"clinical_significance":[],"id":"rs2130424478","seq_region_name":"7","source":"dbSNP","start":140505185,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140505185,"feature_type":"variation","strand":1},{"end":140505186,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140505186,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1191184411","seq_region_name":"7","clinical_significance":[]},{"id":"rs954571443","seq_region_name":"7","clinical_significance":[],"start":140505188,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140505188,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140505193,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505193,"source":"dbSNP","id":"rs1263325519","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs79998812","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505196,"source":"dbSNP","strand":1,"feature_type":"variation","end":140505196,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1394796295","clinical_significance":[],"alleles":["G","A"],"end":140505197,"strand":1,"feature_type":"variation","start":140505197,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1284881970","seq_region_name":"7","end":140505199,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140505199,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795560618","clinical_significance":[],"end":140505201,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140505201,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140505203,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140505203,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795560630","seq_region_name":"7"},{"clinical_significance":[],"id":"rs376025029","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505205,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140505205},{"seq_region_name":"7","id":"rs936600286","clinical_significance":[],"strand":1,"feature_type":"variation","end":140505207,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505207,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs926026382","feature_type":"variation","strand":1,"end":140505208,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505208},{"seq_region_name":"7","id":"rs1160082480","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505211,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140505211},{"clinical_significance":[],"seq_region_name":"7","id":"rs1358122402","source":"dbSNP","start":140505212,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140505212,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1218623899","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505214,"feature_type":"variation","strand":1,"end":140505214,"alleles":["A","G"]},{"start":140505215,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C","G"],"end":140505215,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs936170992","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795560807","end":140505218,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140505218,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140505219,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140505219,"strand":1,"feature_type":"variation","id":"rs1795560827","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140505221,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505221,"clinical_significance":[],"id":"rs191522138","seq_region_name":"7"},{"start":140505223,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140505223,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585524274","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs184040985","source":"dbSNP","start":140505229,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140505229,"alleles":["G","A","C"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505233,"feature_type":"variation","strand":1,"end":140505233,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795561116"},{"seq_region_name":"7","id":"rs1398248860","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505234,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140505234},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140505237,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505237,"source":"dbSNP","seq_region_name":"7","id":"rs1339854597","clinical_significance":[]},{"clinical_significance":[],"id":"rs1313793416","seq_region_name":"7","alleles":["A","G"],"end":140505246,"feature_type":"variation","strand":1,"source":"dbSNP","start":140505246,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs566444040","feature_type":"variation","strand":1,"end":140505247,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505247},{"end":140505250,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140505250,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs950267173","seq_region_name":"7"},{"alleles":["C","A","G"],"end":140505252,"feature_type":"variation","strand":1,"source":"dbSNP","start":140505252,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1045447318"},{"seq_region_name":"7","id":"rs2130424571","clinical_significance":[],"start":140505256,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140505256,"alleles":["T","G"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140505258,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140505258,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795561277","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140505261,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505261,"clinical_significance":[],"id":"rs1795561296","seq_region_name":"7"},{"seq_region_name":"7","id":"rs905544132","clinical_significance":[],"alleles":["G","A","C"],"end":140505268,"strand":1,"feature_type":"variation","start":140505268,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1001178811","seq_region_name":"7","end":140505273,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140505273,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1434131137","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505274,"feature_type":"variation","strand":1,"end":140505274,"alleles":["T","C"]},{"start":140505280,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140505280,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1017101586","clinical_significance":[]},{"start":140505286,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140505286,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795561397","clinical_significance":[]},{"end":140505287,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140505287,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1302435655","clinical_significance":[]},{"alleles":["T","G"],"end":140505293,"feature_type":"variation","strand":1,"source":"dbSNP","start":140505293,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795561432","seq_region_name":"7"},{"source":"dbSNP","start":140505294,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140505294,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1192055009"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505300,"source":"dbSNP","strand":1,"feature_type":"variation","end":140505300,"alleles":["T","G"],"seq_region_name":"7","id":"rs1795561467","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140505301,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505301,"clinical_significance":[],"seq_region_name":"7","id":"rs906623663"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130424597","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505306,"feature_type":"variation","strand":1,"end":140505306,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1261825230","end":140505308,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140505308,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140505309,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140505309,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs898202839"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505310,"feature_type":"variation","strand":1,"end":140505310,"alleles":["G","A"],"clinical_significance":[],"id":"rs994444114","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1025421748","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505311,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140505311},{"seq_region_name":"7","id":"rs1795561578","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140505319,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505319,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795561598","alleles":["G","A"],"end":140505326,"feature_type":"variation","strand":1,"source":"dbSNP","start":140505326,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","A"],"end":140505328,"strand":1,"feature_type":"variation","start":140505328,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795561613","clinical_significance":[]},{"seq_region_name":"7","id":"rs1241196632","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505331,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140505331},{"strand":1,"feature_type":"variation","end":140505332,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505332,"source":"dbSNP","seq_region_name":"7","id":"rs1795561657","clinical_significance":[]},{"clinical_significance":[],"id":"rs1288395478","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140505333,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505333},{"seq_region_name":"7","id":"rs1795561699","clinical_significance":[],"start":140505337,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140505337,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1209193593","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140505338,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505338},{"clinical_significance":[],"seq_region_name":"7","id":"rs1254065464","feature_type":"variation","strand":1,"alleles":["TGTGT","TGT"],"end":140505342,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505338},{"seq_region_name":"7","id":"rs1795561756","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505341,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140505341},{"seq_region_name":"7","id":"rs1795561773","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505346,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140505346},{"alleles":["A","G"],"end":140505347,"strand":1,"feature_type":"variation","start":140505347,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs955316848","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505348,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140505348,"seq_region_name":"7","id":"rs533827711","clinical_significance":[]},{"id":"rs986699888","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505349,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140505349},{"id":"rs1204660461","seq_region_name":"7","clinical_significance":[],"start":140505350,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140505350,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1317436265","clinical_significance":[],"alleles":["C","T"],"end":140505352,"strand":1,"feature_type":"variation","start":140505352,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1585524321","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505353,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140505353},{"seq_region_name":"7","id":"rs888603095","clinical_significance":[],"alleles":["AT","-"],"end":140505354,"strand":1,"feature_type":"variation","start":140505353,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505356,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140505356,"seq_region_name":"7","id":"rs1398050384","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505357,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140505357,"clinical_significance":[],"id":"rs1377288502","seq_region_name":"7"},{"id":"rs1795561982","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505358,"source":"dbSNP","strand":1,"feature_type":"variation","end":140505358,"alleles":["T","G"]},{"end":140505361,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140505361,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1453847644"},{"start":140505362,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140505362,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1443399318","clinical_significance":[]},{"id":"rs1795562043","seq_region_name":"7","clinical_significance":[],"start":140505363,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140505363,"strand":1,"feature_type":"variation"},{"end":140505364,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140505364,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795562061","clinical_significance":[]},{"alleles":["A","T"],"end":140505366,"feature_type":"variation","strand":1,"source":"dbSNP","start":140505366,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795562082"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1005783654","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505370,"feature_type":"variation","strand":1,"end":140505370,"alleles":["G","A"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505375,"source":"dbSNP","strand":1,"feature_type":"variation","end":140505375,"alleles":["C","T"],"seq_region_name":"7","id":"rs1018120407","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795562139","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505378,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140505378},{"source":"dbSNP","start":140505382,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140505382,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1402819592"},{"seq_region_name":"7","id":"rs1192294337","clinical_significance":[],"start":140505385,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140505385,"strand":1,"feature_type":"variation"},{"alleles":["A","C"],"end":140505387,"feature_type":"variation","strand":1,"source":"dbSNP","start":140505387,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130424667"},{"seq_region_name":"7","id":"rs1734326195","clinical_significance":[],"alleles":["G","T"],"end":140505388,"strand":1,"feature_type":"variation","start":140505388,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505391,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140505391,"id":"rs1169242947","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505392,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140505392,"clinical_significance":[],"id":"rs2130424678","seq_region_name":"7"},{"id":"rs1037258202","seq_region_name":"7","clinical_significance":[],"start":140505396,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140505396,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795562243","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505406,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140505406},{"seq_region_name":"7","id":"rs1795562262","clinical_significance":[],"end":140505409,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140505409,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505410,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140505410,"clinical_significance":[],"id":"rs1422353503","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795562305","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505418,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140505418},{"seq_region_name":"7","id":"rs965082451","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505424,"source":"dbSNP","strand":1,"feature_type":"variation","end":140505424,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1440669030","alleles":["C","T"],"end":140505425,"feature_type":"variation","strand":1,"source":"dbSNP","start":140505425,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140505426,"alleles":["T","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505426,"source":"dbSNP","id":"rs745831864","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140505427,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505427,"clinical_significance":[],"id":"rs926069782","seq_region_name":"7"},{"seq_region_name":"7","id":"rs558643019","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505430,"source":"dbSNP","strand":1,"feature_type":"variation","end":140505430,"alleles":["A","C","T"]},{"seq_region_name":"7","id":"rs551741591","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140505432,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505432,"source":"dbSNP"},{"seq_region_name":"7","id":"rs2130424707","clinical_significance":[],"strand":1,"feature_type":"variation","end":140505434,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505434,"source":"dbSNP"},{"source":"dbSNP","start":140505434,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TT","T"],"end":140505435,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1458100023","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795562469","clinical_significance":[],"strand":1,"feature_type":"variation","end":140505437,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505437,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140505439,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505439,"clinical_significance":[],"seq_region_name":"7","id":"rs1795562495"},{"clinical_significance":[],"id":"rs936092258","seq_region_name":"7","source":"dbSNP","start":140505440,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140505440,"alleles":["T","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs989007687","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140505444,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505444,"source":"dbSNP"},{"alleles":["GGG","GG"],"end":140505448,"feature_type":"variation","strand":1,"source":"dbSNP","start":140505446,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1196730597"},{"seq_region_name":"7","id":"rs1795562566","clinical_significance":[],"start":140505448,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140505448,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505449,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140505449,"seq_region_name":"7","id":"rs954516939","clinical_significance":[]},{"end":140505450,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140505450,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs913384469","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140505451,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505451,"clinical_significance":[],"id":"rs950172835","seq_region_name":"7"},{"source":"dbSNP","start":140505452,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140505452,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs187210898"},{"source":"dbSNP","start":140505453,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140505453,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs369596344"},{"seq_region_name":"7","id":"rs1795562714","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505459,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140505459},{"source":"dbSNP","start":140505474,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140505474,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130424730"},{"id":"rs373509252","seq_region_name":"7","clinical_significance":[],"end":140505478,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140505478,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs937003871","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140505479,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505479,"source":"dbSNP"},{"source":"dbSNP","start":140505481,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140505481,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795562765"},{"id":"rs1795562785","seq_region_name":"7","clinical_significance":[],"alleles":["AGAGCTAGGA","A"],"end":140505491,"strand":1,"feature_type":"variation","start":140505482,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1379652197","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505483,"feature_type":"variation","strand":1,"alleles":["GAGCTAGGAAAGGG","GAGCTAGGAAAGGGGAGCTAGGAAAGGG"],"end":140505496},{"id":"rs1329698585","seq_region_name":"7","clinical_significance":[],"alleles":["G","A","T"],"end":140505485,"strand":1,"feature_type":"variation","start":140505485,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1795562843","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505486,"source":"dbSNP","strand":1,"feature_type":"variation","end":140505486,"alleles":["C","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795562860","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505487,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140505487},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585524363","feature_type":"variation","strand":1,"end":140505488,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505488},{"alleles":["G","T"],"end":140505490,"strand":1,"feature_type":"variation","start":140505490,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1038034826","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505492,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140505492,"clinical_significance":[],"seq_region_name":"7","id":"rs1795562936"},{"start":140505494,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140505494,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795562952","clinical_significance":[]},{"alleles":["G","T"],"end":140505495,"feature_type":"variation","strand":1,"source":"dbSNP","start":140505495,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795562970"},{"feature_type":"variation","strand":1,"end":140505496,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505496,"clinical_significance":[],"seq_region_name":"7","id":"rs1295744261"},{"seq_region_name":"7","id":"rs1795563006","clinical_significance":[],"alleles":["T","G"],"end":140505497,"strand":1,"feature_type":"variation","start":140505497,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs966992643","clinical_significance":[],"end":140505498,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140505498,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140505499,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140505499,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795563045","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505500,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140505500,"clinical_significance":[],"id":"rs771717350","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs993861597","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505501,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140505501},{"seq_region_name":"7","id":"rs1439902990","clinical_significance":[],"alleles":["A","G","T"],"end":140505507,"strand":1,"feature_type":"variation","start":140505507,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795563150","source":"dbSNP","start":140505508,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140505508,"alleles":["T","C"],"feature_type":"variation","strand":1},{"start":140505511,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140505511,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795563172","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1381988527","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140505512,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505512},{"alleles":["C","T"],"end":140505514,"strand":1,"feature_type":"variation","start":140505514,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795563216","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1025325965","source":"dbSNP","start":140505517,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140505517,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs775388543","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140505518,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505518,"source":"dbSNP"},{"end":140505521,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140505521,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795563295"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140505524,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505524,"clinical_significance":[],"seq_region_name":"7","id":"rs1795563309"},{"clinical_significance":[],"seq_region_name":"7","id":"rs938139629","alleles":["C","T"],"end":140505525,"feature_type":"variation","strand":1,"source":"dbSNP","start":140505525,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["G","A"],"end":140505527,"feature_type":"variation","strand":1,"source":"dbSNP","start":140505527,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795563350"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795563377","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505532,"feature_type":"variation","strand":1,"end":140505532,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1238528987","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505533,"source":"dbSNP","strand":1,"feature_type":"variation","end":140505533,"alleles":["G","A","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505534,"source":"dbSNP","strand":1,"feature_type":"variation","end":140505534,"alleles":["C","A"],"seq_region_name":"7","id":"rs1055116747","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130424792","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505540,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140505540},{"seq_region_name":"7","id":"rs2130424795","clinical_significance":[],"start":140505541,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140505541,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"start":140505542,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140505542,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585524386","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585524388","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140505548,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505548},{"clinical_significance":[],"seq_region_name":"7","id":"rs537720280","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505549,"feature_type":"variation","strand":1,"end":140505549,"alleles":["G","A"]},{"alleles":["T","G"],"end":140505552,"strand":1,"feature_type":"variation","start":140505552,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1358556702","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140505553,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505553,"clinical_significance":[],"id":"rs1264920072","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140505554,"alleles":["T","A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505554,"clinical_significance":[],"id":"rs1007982385","seq_region_name":"7"},{"alleles":["C","T"],"end":140505555,"feature_type":"variation","strand":1,"source":"dbSNP","start":140505555,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795563541"},{"clinical_significance":[],"id":"rs1217683095","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505557,"feature_type":"variation","strand":1,"end":140505557,"alleles":["A","G"]},{"id":"rs1018151140","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505561,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140505561},{"source":"dbSNP","start":140505562,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140505562,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1585524399","seq_region_name":"7"},{"id":"rs963992184","seq_region_name":"7","clinical_significance":[],"start":140505565,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","T"],"end":140505565,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs760430346","seq_region_name":"7","alleles":["G","A","T"],"end":140505566,"feature_type":"variation","strand":1,"source":"dbSNP","start":140505566,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["A","G"],"end":140505569,"strand":1,"feature_type":"variation","start":140505569,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795563670","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795563688","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505574,"feature_type":"variation","strand":1,"end":140505574,"alleles":["A","G","T"]},{"seq_region_name":"7","id":"rs1585524404","clinical_significance":[],"strand":1,"feature_type":"variation","end":140505579,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505579,"source":"dbSNP"},{"clinical_significance":[],"id":"rs2130424841","seq_region_name":"7","source":"dbSNP","start":140505580,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140505580,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1037121443","source":"dbSNP","start":140505581,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140505581,"alleles":["T","A"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140505584,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505584,"source":"dbSNP","id":"rs1304139305","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795563756","alleles":["G","A"],"end":140505589,"feature_type":"variation","strand":1,"source":"dbSNP","start":140505589,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795563776","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140505590,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505590},{"clinical_significance":[],"seq_region_name":"7","id":"rs191977662","feature_type":"variation","strand":1,"end":140505594,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505594},{"seq_region_name":"7","id":"rs1795563795","clinical_significance":[],"strand":1,"feature_type":"variation","end":140505596,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505596,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1388012063","end":140505597,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140505597,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["G","A"],"end":140505601,"feature_type":"variation","strand":1,"source":"dbSNP","start":140505601,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1301960186","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1200953877","seq_region_name":"7","feature_type":"variation","strand":1,"end":140505604,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505604},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140505606,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505606,"clinical_significance":[],"seq_region_name":"7","id":"rs1248782699"},{"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140505607,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505607,"clinical_significance":[],"seq_region_name":"7","id":"rs1585524418"},{"id":"rs574252978","seq_region_name":"7","clinical_significance":[],"start":140505608,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140505608,"strand":1,"feature_type":"variation"},{"start":140505610,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140505610,"strand":1,"feature_type":"variation","id":"rs1795563936","seq_region_name":"7","clinical_significance":[]},{"id":"rs535581050","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505612,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140505612},{"clinical_significance":[],"seq_region_name":"7","id":"rs763717706","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505616,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140505616},{"clinical_significance":[],"seq_region_name":"7","id":"rs1377982191","source":"dbSNP","start":140505618,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140505618,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["CCC","CC"],"end":140505622,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505620,"source":"dbSNP","seq_region_name":"7","id":"rs1436880519","clinical_significance":[]},{"seq_region_name":"7","id":"rs1200981616","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140505623,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505623,"source":"dbSNP"},{"clinical_significance":[],"id":"rs957709557","seq_region_name":"7","source":"dbSNP","start":140505631,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140505631,"alleles":["C","A","T"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140505632,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140505632,"alleles":["G","A","C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs35619729"},{"source":"dbSNP","start":140505636,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140505636,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1284157683","seq_region_name":"7"},{"seq_region_name":"7","id":"rs185359284","clinical_significance":[],"start":140505638,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140505638,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs9969354","feature_type":"variation","strand":1,"end":140505639,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505639},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795564229","feature_type":"variation","strand":1,"alleles":["A","T"],"end":140505643,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505643},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140505647,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505647,"source":"dbSNP","seq_region_name":"7","id":"rs1795564247","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505651,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140505651,"seq_region_name":"7","id":"rs558160240","clinical_significance":[]},{"start":140505651,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TTT","T"],"end":140505653,"strand":1,"feature_type":"variation","id":"rs1795564297","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505655,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140505655,"id":"rs1331070578","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs927572821","feature_type":"variation","strand":1,"alleles":["C","A","G","T"],"end":140505657,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505657},{"seq_region_name":"7","id":"rs1400096071","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505658,"source":"dbSNP","strand":1,"feature_type":"variation","end":140505658,"alleles":["G","A"]},{"clinical_significance":[],"id":"rs190605623","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140505660,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505660},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795564419","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505664,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140505664},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140505667,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505667,"clinical_significance":[],"seq_region_name":"7","id":"rs1296030853"},{"source":"dbSNP","start":140505668,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140505668,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130424917"},{"clinical_significance":[],"id":"rs1402700804","seq_region_name":"7","alleles":["G","C"],"end":140505672,"feature_type":"variation","strand":1,"source":"dbSNP","start":140505672,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs150856059","alleles":["GAGGAGGA","GAGGA"],"end":140505679,"feature_type":"variation","strand":1,"source":"dbSNP","start":140505672,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130424925","end":140505678,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140505678,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1174079037","clinical_significance":[],"start":140505682,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140505682,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"alleles":["G","C","T"],"end":140505685,"strand":1,"feature_type":"variation","start":140505685,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795564517","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795564534","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140505686,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505686},{"clinical_significance":[],"seq_region_name":"7","id":"rs1021206853","alleles":["G","A"],"end":140505690,"feature_type":"variation","strand":1,"source":"dbSNP","start":140505690,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["G","A"],"end":140505691,"strand":1,"feature_type":"variation","start":140505691,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795564580","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505695,"feature_type":"variation","strand":1,"end":140505699,"alleles":["TTCTT","TT"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795564593"},{"strand":1,"feature_type":"variation","end":140505696,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505696,"source":"dbSNP","id":"rs1377020388","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1038470132","source":"dbSNP","start":140505697,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140505697,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs193135537","clinical_significance":[],"end":140505700,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140505700,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505701,"feature_type":"variation","strand":1,"end":140505701,"alleles":["G","T"],"clinical_significance":[],"id":"rs1795564649","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795564672","feature_type":"variation","strand":1,"end":140505715,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505715},{"clinical_significance":[],"seq_region_name":"7","id":"rs1391105751","source":"dbSNP","start":140505722,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140505722,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140505725,"alleles":["GGGG","GGGGG"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505722,"clinical_significance":[],"seq_region_name":"7","id":"rs1795564723"},{"clinical_significance":[],"id":"rs1478883231","seq_region_name":"7","alleles":["G","A"],"end":140505723,"feature_type":"variation","strand":1,"source":"dbSNP","start":140505723,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140505725,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140505725,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs929617320","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795564784","clinical_significance":[],"end":140505727,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140505727,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1335067791","clinical_significance":[],"start":140505728,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140505728,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505729,"source":"dbSNP","strand":1,"feature_type":"variation","end":140505729,"alleles":["C","T"],"id":"rs966686259","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1046808002","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140505730,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505730},{"clinical_significance":[],"id":"rs2130424967","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140505733,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505733},{"seq_region_name":"7","id":"rs1258488313","clinical_significance":[],"strand":1,"feature_type":"variation","end":140505741,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505741,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505743,"feature_type":"variation","strand":1,"end":140505743,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1292708757"},{"id":"rs1795564900","seq_region_name":"7","clinical_significance":[],"start":140505744,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140505744,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505745,"feature_type":"variation","strand":1,"end":140505745,"alleles":["G","C"],"clinical_significance":[],"id":"rs2130424986","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140505746,"alleles":["G","A","C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505746,"clinical_significance":[],"id":"rs890837394","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505751,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140505751,"seq_region_name":"7","id":"rs1008055727","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140505752,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505752,"clinical_significance":[],"seq_region_name":"7","id":"rs1795565712"},{"source":"dbSNP","start":140505756,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140505756,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1039530999"},{"start":140505760,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140505760,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1319220395","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1344686018","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505762,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140505762},{"clinical_significance":[],"id":"rs148465927","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505764,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140505764},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505770,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140505770,"seq_region_name":"7","id":"rs1795565790","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1259274949","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505774,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140505774},{"clinical_significance":[],"seq_region_name":"7","id":"rs1220998135","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505782,"feature_type":"variation","strand":1,"end":140505782,"alleles":["A","G"]},{"strand":1,"feature_type":"variation","end":140505784,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505784,"source":"dbSNP","id":"rs1319453683","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505794,"source":"dbSNP","strand":1,"feature_type":"variation","end":140505794,"alleles":["T","G"],"id":"rs1275729213","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140505795,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140505795,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795567736"},{"end":140505801,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140505801,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1429635488"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505802,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140505802,"clinical_significance":[],"seq_region_name":"7","id":"rs1795567771"},{"source":"dbSNP","start":140505803,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140505803,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795567789","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140505813,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505813,"source":"dbSNP","id":"rs1795567807","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs559943201","source":"dbSNP","start":140505814,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140505814,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140505816,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505816,"clinical_significance":[],"id":"rs1032648752","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs957370084","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505817,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140505817},{"seq_region_name":"7","id":"rs1585524527","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505824,"source":"dbSNP","strand":1,"feature_type":"variation","end":140505824,"alleles":["G","A"]},{"end":140505825,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140505825,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1250041280","clinical_significance":[]},{"alleles":["G","A"],"end":140505826,"strand":1,"feature_type":"variation","start":140505826,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795567978","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs959385828","clinical_significance":[],"start":140505827,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140505827,"strand":1,"feature_type":"variation"},{"start":140505829,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140505829,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs56298549","clinical_significance":[]},{"seq_region_name":"7","id":"rs77285844","clinical_significance":[],"end":140505831,"alleles":["A","C","T"],"strand":1,"feature_type":"variation","start":140505831,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs909971897","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140505832,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505832},{"source":"dbSNP","start":140505833,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140505833,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795568108"},{"clinical_significance":[],"id":"rs1795568122","seq_region_name":"7","source":"dbSNP","start":140505834,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140505834,"alleles":["T","A","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1473141387","alleles":["G","T"],"end":140505842,"feature_type":"variation","strand":1,"source":"dbSNP","start":140505842,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs2074084926","clinical_significance":[],"start":140505843,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140505843,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505844,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CAGGGTTGGTTTCTTCTGAGGTCTCTC","C"],"end":140505870,"seq_region_name":"7","id":"rs1795568171","clinical_significance":[]},{"seq_region_name":"7","id":"rs541258452","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505848,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140505848},{"seq_region_name":"7","id":"rs1044255716","clinical_significance":[],"end":140505849,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140505849,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795568243","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140505851,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505851,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585524553","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505853,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140505853},{"id":"rs1185611224","seq_region_name":"7","clinical_significance":[],"end":140505860,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140505860,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["A","G"],"end":140505862,"feature_type":"variation","strand":1,"source":"dbSNP","start":140505862,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs941446335"},{"id":"rs1795568311","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140505864,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505864,"source":"dbSNP"},{"source":"dbSNP","start":140505866,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140505866,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1037235885"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1257858522","source":"dbSNP","start":140505867,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140505867,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1020381806","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140505868,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505868,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795568393","feature_type":"variation","strand":1,"end":140505870,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505870},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140505873,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505873,"clinical_significance":[],"seq_region_name":"7","id":"rs1585524563"},{"clinical_significance":[],"id":"rs934282372","seq_region_name":"7","feature_type":"variation","strand":1,"end":140505875,"alleles":["CTT","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505873},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505880,"feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140505880,"clinical_significance":[],"seq_region_name":"7","id":"rs1795568442"},{"strand":1,"feature_type":"variation","end":140505886,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505886,"source":"dbSNP","id":"rs1795568476","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs542522815","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505888,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140505888},{"end":140505889,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140505889,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs184378469"},{"seq_region_name":"7","id":"rs981638164","clinical_significance":[],"end":140505893,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140505893,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs112391552","clinical_significance":[],"strand":1,"feature_type":"variation","end":140505896,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505896,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140505898,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505898,"clinical_significance":[],"id":"rs890016760","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140505899,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505899,"source":"dbSNP","seq_region_name":"7","id":"rs1263203675","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505900,"feature_type":"variation","strand":1,"end":140505900,"alleles":["C","T"],"clinical_significance":[],"id":"rs1478794877","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795568678","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505901,"feature_type":"variation","strand":1,"end":140505901,"alleles":["C","T"]},{"alleles":["T","C"],"end":140505903,"feature_type":"variation","strand":1,"source":"dbSNP","start":140505903,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795568702","seq_region_name":"7"},{"id":"rs758973868","seq_region_name":"7","clinical_significance":[],"start":140505905,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140505905,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505907,"source":"dbSNP","strand":1,"feature_type":"variation","end":140505907,"alleles":["C","G"],"seq_region_name":"7","id":"rs1448669857","clinical_significance":[]},{"id":"rs1795568834","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140505909,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505909,"source":"dbSNP"},{"source":"dbSNP","start":140505911,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140505911,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1398058429"},{"source":"dbSNP","start":140505912,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140505912,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795568876"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505913,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140505913,"clinical_significance":[],"seq_region_name":"7","id":"rs943025318"},{"clinical_significance":[],"id":"rs771381074","seq_region_name":"7","alleles":["A","G"],"end":140505914,"feature_type":"variation","strand":1,"source":"dbSNP","start":140505914,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140505915,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505915,"clinical_significance":[],"seq_region_name":"7","id":"rs1795568941"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505918,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140505918,"seq_region_name":"7","id":"rs1563107856","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["TCTCTCT","TCT"],"end":140505925,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505919,"clinical_significance":[],"seq_region_name":"7","id":"rs1795568978"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140505921,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505921,"clinical_significance":[],"id":"rs1795568992","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1416051823","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505922,"source":"dbSNP","strand":1,"feature_type":"variation","end":140505922,"alleles":["C","T"]},{"source":"dbSNP","start":140505928,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140505928,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795569033"},{"id":"rs959105116","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505934,"source":"dbSNP","strand":1,"feature_type":"variation","end":140505934,"alleles":["C","T"]},{"alleles":["T","C"],"end":140505935,"feature_type":"variation","strand":1,"source":"dbSNP","start":140505935,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795569081"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1161734504","feature_type":"variation","strand":1,"end":140505936,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505936},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505939,"source":"dbSNP","strand":1,"feature_type":"variation","end":140505939,"alleles":["T","C"],"id":"rs188013449","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1444208807","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140505940,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505940},{"strand":1,"feature_type":"variation","end":140505942,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505942,"source":"dbSNP","seq_region_name":"7","id":"rs1795569172","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140505943,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505943,"clinical_significance":[],"seq_region_name":"7","id":"rs1795569346"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505945,"source":"dbSNP","strand":1,"feature_type":"variation","end":140505959,"alleles":["TTTCTTTCTTTCTTT","TTTCTTTCTTT","TTTCTTTCTTTCTTTCTTT"],"seq_region_name":"7","id":"rs1466342196","clinical_significance":[]},{"clinical_significance":[],"id":"rs1038682779","seq_region_name":"7","feature_type":"variation","strand":1,"end":140505949,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505949},{"strand":1,"feature_type":"variation","end":140505951,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505951,"source":"dbSNP","seq_region_name":"7","id":"rs1795569452","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs570081629","source":"dbSNP","start":140505957,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140505957,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1438169084","clinical_significance":[],"alleles":["TTTTTTTT","TTTTTTT","TTTTTTTTT"],"end":140505964,"strand":1,"feature_type":"variation","start":140505957,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1232822713","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140505962,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505962},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505963,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140505963,"clinical_significance":[],"seq_region_name":"7","id":"rs1795569619"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505969,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140505969,"clinical_significance":[],"id":"rs35122880","seq_region_name":"7"},{"end":140505970,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140505970,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs920139642","seq_region_name":"7"},{"id":"rs751903955","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505972,"source":"dbSNP","strand":1,"feature_type":"variation","end":140505972,"alleles":["A","T"]},{"id":"rs1795569830","seq_region_name":"7","clinical_significance":[],"start":140505974,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140505974,"strand":1,"feature_type":"variation"},{"start":140505977,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C","T"],"end":140505977,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs10266532","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505978,"feature_type":"variation","strand":1,"end":140505978,"alleles":["G","A"],"clinical_significance":[],"id":"rs1046713222","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505979,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140505979,"id":"rs1795570090","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795570124","source":"dbSNP","start":140505981,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140505981,"feature_type":"variation","strand":1},{"id":"rs912346888","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505983,"source":"dbSNP","strand":1,"feature_type":"variation","end":140505983,"alleles":["G","A"]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140505988,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140505988,"source":"dbSNP","id":"rs1795570167","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505989,"feature_type":"variation","strand":1,"end":140505989,"alleles":["C","T"],"clinical_significance":[],"id":"rs796797030","seq_region_name":"7"},{"seq_region_name":"7","id":"rs943776708","clinical_significance":[],"start":140505990,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140505990,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1795570227","seq_region_name":"7","feature_type":"variation","strand":1,"end":140505992,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505992},{"clinical_significance":[],"id":"rs1795570264","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140505994,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140505994},{"clinical_significance":[],"id":"rs1437088727","seq_region_name":"7","source":"dbSNP","start":140506000,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140506000,"alleles":["G","T"],"feature_type":"variation","strand":1},{"start":140506003,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140506003,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795570319","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795570350","clinical_significance":[],"strand":1,"feature_type":"variation","end":140506004,"alleles":["T","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506004,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795570400","clinical_significance":[],"start":140506009,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140506009,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1307373322","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506010,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140506010},{"seq_region_name":"7","id":"rs1795570456","clinical_significance":[],"start":140506011,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140506011,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140506015,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506015,"source":"dbSNP","seq_region_name":"7","id":"rs1795570473","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140506016,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506016,"clinical_significance":[],"id":"rs1234454505","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506021,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140506021,"clinical_significance":[],"seq_region_name":"7","id":"rs1258061740"},{"source":"dbSNP","start":140506022,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140506022,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs2130425228","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140506030,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506030,"source":"dbSNP","seq_region_name":"7","id":"rs1795570544","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140506031,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506031,"clinical_significance":[],"seq_region_name":"7","id":"rs1039966517"},{"alleles":["C","A"],"end":140506038,"feature_type":"variation","strand":1,"source":"dbSNP","start":140506038,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs959241409"},{"end":140506044,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140506044,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1361435352","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs990818670","seq_region_name":"7","source":"dbSNP","start":140506048,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140506048,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795570643","alleles":["T","A"],"end":140506049,"feature_type":"variation","strand":1,"source":"dbSNP","start":140506049,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1438226614","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140506057,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506057,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1407708171","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506061,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140506061},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506065,"feature_type":"variation","strand":1,"end":140506065,"alleles":["A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1209688648"},{"seq_region_name":"7","id":"rs1192336991","clinical_significance":[],"strand":1,"feature_type":"variation","end":140506066,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506066,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1479273056","clinical_significance":[],"strand":1,"feature_type":"variation","end":140506067,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506067,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795570730","alleles":["A","G"],"end":140506073,"feature_type":"variation","strand":1,"source":"dbSNP","start":140506073,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["T","C"],"end":140506075,"feature_type":"variation","strand":1,"source":"dbSNP","start":140506075,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795570746"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795570762","end":140506079,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140506079,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1795570785","seq_region_name":"7","end":140506083,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140506083,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506087,"source":"dbSNP","strand":1,"feature_type":"variation","end":140506087,"alleles":["C","G"],"seq_region_name":"7","id":"rs899683012","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1016882198","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506089,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140506089},{"id":"rs140626016","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506091,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140506091},{"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140506092,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506092,"clinical_significance":[],"id":"rs7795188","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs892347642","source":"dbSNP","start":140506093,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140506093,"feature_type":"variation","strand":1},{"alleles":["G","A","C","T"],"end":140506094,"feature_type":"variation","strand":1,"source":"dbSNP","start":140506094,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs151249273","seq_region_name":"7"},{"id":"rs1020287073","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506095,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140506095},{"clinical_significance":[],"id":"rs1585524637","seq_region_name":"7","source":"dbSNP","start":140506096,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140506096,"alleles":["A","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795571108","feature_type":"variation","strand":1,"end":140506097,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506097},{"alleles":["A","C","G"],"end":140506099,"strand":1,"feature_type":"variation","start":140506099,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs907312160","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795571168","feature_type":"variation","strand":1,"end":140506100,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506100},{"clinical_significance":[],"seq_region_name":"7","id":"rs566191174","source":"dbSNP","start":140506102,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C","G"],"end":140506102,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1002979474","clinical_significance":[],"strand":1,"feature_type":"variation","end":140506103,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506103,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140506104,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506104,"clinical_significance":[],"seq_region_name":"7","id":"rs539911325"},{"clinical_significance":[],"id":"rs558196966","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140506105,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506105},{"start":140506106,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140506106,"alleles":["C","A"],"strand":1,"feature_type":"variation","id":"rs760847176","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","T"],"end":140506108,"strand":1,"feature_type":"variation","start":140506108,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1345015030","clinical_significance":[]},{"source":"dbSNP","start":140506109,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140506109,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1177289089"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1416472326","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506111,"feature_type":"variation","strand":1,"alleles":["T","TT"],"end":140506111},{"id":"rs1795571367","seq_region_name":"7","clinical_significance":[],"alleles":["TAT","T"],"end":140506113,"strand":1,"feature_type":"variation","start":140506111,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795571383","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["TATTT","T"],"end":140506115,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506111,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1554454807","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["TATTTTT","T"],"end":140506117,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506111,"source":"dbSNP"},{"id":"rs747592322","seq_region_name":"7","clinical_significance":[],"start":140506111,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140506118,"alleles":["TATTTTTT","T"],"strand":1,"feature_type":"variation"},{"alleles":["TATTTTTTT","T"],"end":140506119,"strand":1,"feature_type":"variation","start":140506111,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs777000321","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1263261836","end":140506112,"alleles":["A","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140506112,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["A","-"],"end":140506112,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506112,"source":"dbSNP","seq_region_name":"7","id":"rs1795571483","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506113,"source":"dbSNP","strand":1,"feature_type":"variation","end":140506133,"alleles":["TTTTTTTTTTTTTTTTTTTTT","TTTTTTT","TTTTTTTT","TTTTTTTTT","TTTTTTTTTT","TTTTTTTTTTT","TTTTTTTTTTTT","TTTTTTTTTTTTT","TTTTTTTTTTTTTT","TTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT"],"id":"rs759828428","seq_region_name":"7","clinical_significance":[]},{"end":140506113,"alleles":["-","C"],"strand":1,"feature_type":"variation","start":140506114,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130425370","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506115,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140506115,"clinical_significance":[],"seq_region_name":"7","id":"rs1795571782"},{"end":140506115,"alleles":["-","A","G"],"strand":1,"feature_type":"variation","start":140506116,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795571804","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs958912082","source":"dbSNP","start":140506116,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A","C"],"end":140506116,"feature_type":"variation","strand":1},{"alleles":["T","A"],"end":140506118,"strand":1,"feature_type":"variation","start":140506118,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585524688","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506119,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140506119,"seq_region_name":"7","id":"rs1450644739","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs974609627","end":140506120,"alleles":["T","A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140506120,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140506121,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506121,"clinical_significance":[],"seq_region_name":"7","id":"rs1795571926"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140506122,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506122,"source":"dbSNP","seq_region_name":"7","id":"rs1795571940","clinical_significance":[]},{"id":"rs911482128","seq_region_name":"7","clinical_significance":[],"start":140506123,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140506123,"alleles":["T","C","G"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["T","A","G"],"end":140506127,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506127,"source":"dbSNP","seq_region_name":"7","id":"rs1476192469","clinical_significance":[]},{"seq_region_name":"7","id":"rs1303929682","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506128,"source":"dbSNP","strand":1,"feature_type":"variation","end":140506128,"alleles":["T","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1387793314","end":140506135,"alleles":["TTTTTTGT","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140506128,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140506129,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140506129,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1585524699","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["TTTTTGT","T"],"end":140506135,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506129,"clinical_significance":[],"seq_region_name":"7","id":"rs1795572103"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795572131","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140506130,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506130},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506130,"feature_type":"variation","strand":1,"end":140506140,"alleles":["TTTTGTATTTT","TTTT"],"clinical_significance":[],"seq_region_name":"7","id":"rs1563107943"},{"seq_region_name":"7","id":"rs1795572173","clinical_significance":[],"start":140506131,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140506139,"alleles":["TTTGTATTT","TTT"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140506132,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140506132,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1426167228","seq_region_name":"7"},{"start":140506133,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140506133,"strand":1,"feature_type":"variation","id":"rs1418364252","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["TGT","T"],"end":140506135,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506133,"source":"dbSNP","seq_region_name":"7","id":"rs1795572248","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506134,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140506134,"seq_region_name":"7","id":"rs1026494804","clinical_significance":[]},{"seq_region_name":"7","id":"rs1182013626","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","-"],"end":140506134,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506134,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795572319","clinical_significance":[],"end":140506136,"alleles":["GTA","-"],"strand":1,"feature_type":"variation","start":140506134,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs150455556","alleles":["T","G"],"end":140506135,"feature_type":"variation","strand":1,"source":"dbSNP","start":140506135,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs886218278","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506136,"feature_type":"variation","strand":1,"alleles":["A","C","T"],"end":140506136},{"end":140506137,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140506137,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs942930621","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1355334968","end":140506140,"alleles":["TT","TTTTTTTTTTTTTTGTT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140506139,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140506140,"alleles":["T","TTTTTTTTGT"],"strand":1,"feature_type":"variation","start":140506140,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1554454818","seq_region_name":"7","clinical_significance":[]},{"end":140506141,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140506141,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1480506264","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795573328","feature_type":"variation","strand":1,"end":140506155,"alleles":["ACGTAGAGATGGGGG","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506141},{"feature_type":"variation","strand":1,"alleles":["C","A","G","T"],"end":140506142,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506142,"clinical_significance":[],"seq_region_name":"7","id":"rs1259586711"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506143,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140506143,"seq_region_name":"7","id":"rs1488777987","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1250947740","source":"dbSNP","start":140506149,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140506149,"alleles":["A","G","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795573414","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506150,"source":"dbSNP","strand":1,"feature_type":"variation","end":140506150,"alleles":["T","A"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506151,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140506151,"id":"rs1795573435","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506154,"source":"dbSNP","strand":1,"feature_type":"variation","end":140506154,"alleles":["G","C","T"],"seq_region_name":"7","id":"rs1585524728","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506156,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140506156,"seq_region_name":"7","id":"rs1585524730","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1027278541","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506161,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140506161},{"clinical_significance":[],"seq_region_name":"7","id":"rs1230230939","feature_type":"variation","strand":1,"end":140506161,"alleles":["C","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506161},{"end":140506162,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140506162,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs951624037"},{"clinical_significance":[],"id":"rs982441945","seq_region_name":"7","source":"dbSNP","start":140506163,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140506163,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795573600","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140506169,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506169,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1178962043","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506170,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140506170},{"clinical_significance":[],"seq_region_name":"7","id":"rs1177925872","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506173,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140506173},{"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140506176,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506176,"source":"dbSNP","seq_region_name":"7","id":"rs571245847","clinical_significance":[]},{"clinical_significance":[],"id":"rs1381160906","seq_region_name":"7","alleles":["A","C"],"end":140506182,"feature_type":"variation","strand":1,"source":"dbSNP","start":140506182,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795573902","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140506185,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506185,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140506188,"alleles":["CC","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506187,"clinical_significance":[],"seq_region_name":"7","id":"rs1460028496"},{"end":140506189,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140506189,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1353408368","clinical_significance":[]},{"id":"rs1421067487","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506190,"source":"dbSNP","strand":1,"feature_type":"variation","end":140506190,"alleles":["G","C"]},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140506191,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506191,"source":"dbSNP","id":"rs1795574003","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140506192,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506192,"source":"dbSNP","seq_region_name":"7","id":"rs201238314","clinical_significance":[]},{"id":"rs1344665888","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506193,"source":"dbSNP","strand":1,"feature_type":"variation","end":140506193,"alleles":["C","T"]},{"feature_type":"variation","strand":1,"end":140506195,"alleles":["C","CC"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506195,"clinical_significance":[],"seq_region_name":"7","id":"rs1182781540"},{"strand":1,"feature_type":"variation","end":140506197,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506197,"source":"dbSNP","seq_region_name":"7","id":"rs1795574124","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs544128896","end":140506198,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140506198,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140506204,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140506204,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1239942439","clinical_significance":[]},{"clinical_significance":[],"id":"rs1194004819","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506210,"feature_type":"variation","strand":1,"end":140506210,"alleles":["C","T"]},{"end":140506214,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140506214,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs975202264","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140506219,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506219,"clinical_significance":[],"seq_region_name":"7","id":"rs1266091288"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506221,"feature_type":"variation","strand":1,"end":140506221,"alleles":["C","T"],"clinical_significance":[],"id":"rs1328512360","seq_region_name":"7"},{"seq_region_name":"7","id":"rs946472824","clinical_significance":[],"start":140506227,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140506227,"strand":1,"feature_type":"variation"},{"alleles":["TGGGATTACAGGCATG","TG"],"end":140506244,"strand":1,"feature_type":"variation","start":140506229,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795574369","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140506230,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140506230,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795574386"},{"seq_region_name":"7","id":"rs1795574412","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140506237,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506237,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140506238,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506238,"source":"dbSNP","id":"rs1314566772","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506239,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140506239,"clinical_significance":[],"id":"rs1241341097","seq_region_name":"7"},{"end":140506242,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140506242,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795574467","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1440644497","source":"dbSNP","start":140506243,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140506243,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1310360621","clinical_significance":[],"end":140506244,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140506244,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs920978243","seq_region_name":"7","source":"dbSNP","start":140506245,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140506245,"alleles":["A","C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1305577992","clinical_significance":[],"end":140506247,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140506247,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140506253,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140506253,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795574559"},{"start":140506254,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140506254,"alleles":["A","T"],"strand":1,"feature_type":"variation","id":"rs180874848","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs11983491","seq_region_name":"7","source":"dbSNP","start":140506256,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140506256,"alleles":["C","A","G","T"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140506259,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140506259,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1003788679"},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140506260,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506260,"source":"dbSNP","id":"rs1054024053","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","T"],"end":140506261,"strand":1,"feature_type":"variation","start":140506261,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1363347417","clinical_significance":[]},{"alleles":["C","T"],"end":140506262,"feature_type":"variation","strand":1,"source":"dbSNP","start":140506262,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795574778"},{"start":140506265,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140506265,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1162462141","clinical_significance":[]},{"start":140506266,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140506266,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795574827","clinical_significance":[]},{"alleles":["C","G"],"end":140506270,"strand":1,"feature_type":"variation","start":140506270,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130425563","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506273,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140506273,"seq_region_name":"7","id":"rs1795574850","clinical_significance":[]},{"id":"rs1034856423","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140506281,"strand":1,"feature_type":"variation","start":140506281,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs895100651","clinical_significance":[],"start":140506282,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140506282,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795574889","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506286,"feature_type":"variation","strand":1,"end":140506286,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795574908","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506290,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140506290},{"alleles":["C","A"],"end":140506291,"strand":1,"feature_type":"variation","start":140506291,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795574928","clinical_significance":[]},{"seq_region_name":"7","id":"rs541640173","clinical_significance":[],"alleles":["A","T"],"end":140506292,"strand":1,"feature_type":"variation","start":140506292,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130425584","feature_type":"variation","strand":1,"end":140506293,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506293},{"start":140506294,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140506294,"strand":1,"feature_type":"variation","id":"rs1246984698","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795575027","clinical_significance":[],"start":140506298,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140506298,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140506299,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506299,"source":"dbSNP","id":"rs945261084","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795575164","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140506300,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506300},{"alleles":["T","G"],"end":140506301,"feature_type":"variation","strand":1,"source":"dbSNP","start":140506301,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1046325832","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140506305,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506305,"source":"dbSNP","seq_region_name":"7","id":"rs1267919616","clinical_significance":[]},{"source":"dbSNP","start":140506307,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140506307,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795575207"},{"clinical_significance":[],"id":"rs1795575231","seq_region_name":"7","alleles":["C","A"],"end":140506310,"feature_type":"variation","strand":1,"source":"dbSNP","start":140506310,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1585524807","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140506312,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506312,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506319,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140506319,"clinical_significance":[],"seq_region_name":"7","id":"rs1193010352"},{"seq_region_name":"7","id":"rs1795575260","clinical_significance":[],"start":140506323,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140506323,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"start":140506329,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140506329,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs559664042","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795575325","seq_region_name":"7","source":"dbSNP","start":140506330,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140506330,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1016911544","clinical_significance":[],"strand":1,"feature_type":"variation","end":140506334,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506334,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506335,"source":"dbSNP","strand":1,"feature_type":"variation","end":140506335,"alleles":["T","A","G"],"seq_region_name":"7","id":"rs907218722","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130425622","clinical_significance":[],"strand":1,"feature_type":"variation","end":140506336,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506336,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1291320893","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140506338,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506338,"source":"dbSNP"},{"id":"rs962702077","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506349,"source":"dbSNP","strand":1,"feature_type":"variation","end":140506349,"alleles":["C","A","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1003253964","feature_type":"variation","strand":1,"end":140506350,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506350},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506353,"source":"dbSNP","strand":1,"feature_type":"variation","end":140506353,"alleles":["A","G","T"],"seq_region_name":"7","id":"rs1795575575","clinical_significance":[]},{"alleles":["T","C"],"end":140506364,"strand":1,"feature_type":"variation","start":140506364,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795575608","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795575637","clinical_significance":[],"start":140506365,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140506365,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795575677","feature_type":"variation","strand":1,"end":140506375,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506375},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506378,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140506378,"clinical_significance":[],"id":"rs1199074362","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506379,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140506379,"clinical_significance":[],"seq_region_name":"7","id":"rs1795575741"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1034442552","source":"dbSNP","start":140506380,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140506380,"alleles":["T","A","G"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140506385,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506385,"source":"dbSNP","seq_region_name":"7","id":"rs527398289","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1332202012","feature_type":"variation","strand":1,"end":140506388,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506388},{"feature_type":"variation","strand":1,"alleles":["G","C","T"],"end":140506393,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506393,"clinical_significance":[],"id":"rs894550042","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140506395,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506395,"source":"dbSNP","id":"rs1026156390","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140506396,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140506396,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs995724473"},{"source":"dbSNP","start":140506401,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140506401,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1302213843","seq_region_name":"7"},{"end":140506404,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140506404,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1400206874","clinical_significance":[]},{"start":140506406,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C","T"],"end":140506406,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795576036","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795576070","alleles":["T","G"],"end":140506410,"feature_type":"variation","strand":1,"source":"dbSNP","start":140506410,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1175671623","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506420,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140506420},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506428,"source":"dbSNP","strand":1,"feature_type":"variation","end":140506428,"alleles":["C","G","T"],"seq_region_name":"7","id":"rs987416724","clinical_significance":[]},{"alleles":["G","T"],"end":140506430,"feature_type":"variation","strand":1,"source":"dbSNP","start":140506430,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs545452612"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506433,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140506433,"seq_region_name":"7","id":"rs1424460817","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795576241","clinical_significance":[],"alleles":["A","T"],"end":140506434,"strand":1,"feature_type":"variation","start":140506434,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506435,"feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140506435,"clinical_significance":[],"seq_region_name":"7","id":"rs1795576266"},{"end":140506436,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140506436,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795576297"},{"feature_type":"variation","strand":1,"alleles":["AA","A"],"end":140506437,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506436,"clinical_significance":[],"id":"rs942961407","seq_region_name":"7"},{"source":"dbSNP","start":140506438,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140506438,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs951655264"},{"seq_region_name":"7","id":"rs1268249108","clinical_significance":[],"end":140506439,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140506439,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["G","C"],"end":140506443,"feature_type":"variation","strand":1,"source":"dbSNP","start":140506443,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs983013786"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506448,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140506448,"seq_region_name":"7","id":"rs1795576444","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1194714101","source":"dbSNP","start":140506449,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140506449,"feature_type":"variation","strand":1},{"start":140506451,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C","G"],"end":140506451,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1489375807","clinical_significance":[]},{"source":"dbSNP","start":140506456,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140506456,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1259866646","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1019796040","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506459,"source":"dbSNP","strand":1,"feature_type":"variation","end":140506459,"alleles":["G","A"]},{"alleles":["T","C"],"end":140506466,"feature_type":"variation","strand":1,"source":"dbSNP","start":140506466,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs756248375","seq_region_name":"7"},{"start":140506471,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140506471,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795576644","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140506475,"alleles":["CCCCC","CCCC"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506471,"source":"dbSNP","id":"rs2130425707","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140506472,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506472,"source":"dbSNP","seq_region_name":"7","id":"rs1795576672","clinical_significance":[]},{"end":140506473,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140506473,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795576702"},{"end":140506474,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140506474,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs946389470","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795576756","clinical_significance":[],"start":140506475,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140506475,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140506477,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506477,"clinical_significance":[],"seq_region_name":"7","id":"rs965080452"},{"clinical_significance":[],"id":"rs1222212332","seq_region_name":"7","source":"dbSNP","start":140506482,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140506482,"alleles":["A","G"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140506483,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140506483,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs375359248"},{"source":"dbSNP","start":140506485,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140506485,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1282059216","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1795576900","seq_region_name":"7","feature_type":"variation","strand":1,"end":140506486,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506486},{"clinical_significance":[],"seq_region_name":"7","id":"rs975444961","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506488,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140506488},{"clinical_significance":[],"seq_region_name":"7","id":"rs139285867","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506492,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140506492},{"clinical_significance":[],"seq_region_name":"7","id":"rs1356616534","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506493,"feature_type":"variation","strand":1,"end":140506493,"alleles":["G","C","T"]},{"end":140506494,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140506494,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795577035","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1315710788","feature_type":"variation","strand":1,"end":140506499,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506499},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140506500,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506500,"source":"dbSNP","seq_region_name":"7","id":"rs921060314","clinical_significance":[]},{"seq_region_name":"7","id":"rs1381441754","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140506503,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506503,"source":"dbSNP"},{"alleles":["TCCTTT","T"],"end":140506508,"strand":1,"feature_type":"variation","start":140506503,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130425745","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506504,"feature_type":"variation","strand":1,"end":140506504,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1402633600"},{"seq_region_name":"7","id":"rs1795577144","clinical_significance":[],"alleles":["C","A"],"end":140506516,"strand":1,"feature_type":"variation","start":140506516,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506517,"feature_type":"variation","strand":1,"end":140506517,"alleles":["T","G"],"clinical_significance":[],"id":"rs1338683702","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140506520,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506520,"clinical_significance":[],"seq_region_name":"7","id":"rs1795577172"},{"id":"rs1468145884","seq_region_name":"7","clinical_significance":[],"end":140506521,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140506521,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1439618295","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140506522,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506522},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795577240","source":"dbSNP","start":140506524,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140506524,"alleles":["T","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs923725160","seq_region_name":"7","alleles":["G","A"],"end":140506526,"feature_type":"variation","strand":1,"source":"dbSNP","start":140506526,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140506527,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140506527,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs939106877"},{"seq_region_name":"7","id":"rs1371561978","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506530,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140506530},{"id":"rs2130425780","seq_region_name":"7","clinical_significance":[],"start":140506532,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140506532,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140506534,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506534,"clinical_significance":[],"seq_region_name":"7","id":"rs1795577336"},{"end":140506537,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140506537,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1192742635","clinical_significance":[]},{"id":"rs1795577426","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506544,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140506544},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506546,"feature_type":"variation","strand":1,"end":140506546,"alleles":["A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs531253202"},{"source":"dbSNP","start":140506546,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AGAGTAAATAGGCTAGAGT","AGAGT"],"end":140506564,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1000032430"},{"seq_region_name":"7","id":"rs1795577546","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506554,"source":"dbSNP","strand":1,"feature_type":"variation","end":140506554,"alleles":["T","C"]},{"feature_type":"variation","strand":1,"end":140506557,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506557,"clinical_significance":[],"id":"rs1795577571","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1258681247","feature_type":"variation","strand":1,"end":140506558,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506558},{"seq_region_name":"7","id":"rs777956563","clinical_significance":[],"end":140506561,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140506561,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506563,"feature_type":"variation","strand":1,"end":140506563,"alleles":["G","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795578153"},{"end":140506564,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140506564,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1585524883","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140506566,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506566,"clinical_significance":[],"seq_region_name":"7","id":"rs1795578207"},{"clinical_significance":[],"id":"rs1585524887","seq_region_name":"7","source":"dbSNP","start":140506569,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140506569,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1461291368","clinical_significance":[],"end":140506570,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140506570,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506571,"feature_type":"variation","strand":1,"end":140506571,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs913757204"},{"alleles":["G","C","T"],"end":140506583,"strand":1,"feature_type":"variation","start":140506583,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795578326","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140506586,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506586,"source":"dbSNP","id":"rs185274140","seq_region_name":"7","clinical_significance":[]},{"id":"rs1218719941","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506588,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140506588},{"clinical_significance":[],"id":"rs1795578402","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140506589,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506589},{"id":"rs1340771169","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140506590,"strand":1,"feature_type":"variation","start":140506590,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506596,"feature_type":"variation","strand":1,"end":140506598,"alleles":["GGG","GG"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795578454"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795578482","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506597,"feature_type":"variation","strand":1,"end":140506597,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1268115733","clinical_significance":[],"start":140506598,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140506598,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1795578541","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506599,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140506599},{"end":140506603,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140506603,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795578569"},{"clinical_significance":[],"seq_region_name":"7","id":"rs945165507","end":140506604,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140506604,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140506610,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140506610,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1226218467","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs537543970","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506611,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140506611},{"clinical_significance":[],"seq_region_name":"7","id":"rs1316851066","feature_type":"variation","strand":1,"end":140506615,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506615},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795578724","source":"dbSNP","start":140506616,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140506616,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795578754","clinical_significance":[],"start":140506620,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140506620,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["TTTTTTTTT","TTTT","TTTTTTTT","TTTTTTTTTT"],"end":140506629,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506621,"source":"dbSNP","seq_region_name":"7","id":"rs1038262706","clinical_significance":[]},{"source":"dbSNP","start":140506622,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140506622,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795578859","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140506629,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506629,"source":"dbSNP","id":"rs1290864243","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs529153045","clinical_significance":[],"strand":1,"feature_type":"variation","end":140506632,"alleles":["G","C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506632,"source":"dbSNP"},{"start":140506637,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140506637,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs559138870","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1331876496","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506640,"feature_type":"variation","strand":1,"end":140506640,"alleles":["G","A"]},{"alleles":["G","A"],"end":140506643,"strand":1,"feature_type":"variation","start":140506643,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795579017","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506644,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140506644,"clinical_significance":[],"seq_region_name":"7","id":"rs188726687"},{"strand":1,"feature_type":"variation","end":140506647,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506647,"source":"dbSNP","seq_region_name":"7","id":"rs1219147500","clinical_significance":[]},{"end":140506648,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140506648,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs898383168","clinical_significance":[]},{"id":"rs1274907525","seq_region_name":"7","clinical_significance":[],"start":140506649,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140506649,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140506654,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506654,"clinical_significance":[],"seq_region_name":"7","id":"rs1795579175"},{"clinical_significance":[],"id":"rs1305550091","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506655,"feature_type":"variation","strand":1,"end":140506655,"alleles":["T","C"]},{"alleles":["A","G"],"end":140506660,"feature_type":"variation","strand":1,"source":"dbSNP","start":140506660,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs547170179"},{"seq_region_name":"7","id":"rs1795579257","clinical_significance":[],"start":140506662,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C"],"end":140506662,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140506671,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506671,"source":"dbSNP","seq_region_name":"7","id":"rs994579939","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506673,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140506673,"seq_region_name":"7","id":"rs1202766741","clinical_significance":[]},{"id":"rs565907680","seq_region_name":"7","clinical_significance":[],"start":140506675,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140506675,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795579387","source":"dbSNP","start":140506677,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140506677,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs2130425884","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506681,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140506681},{"clinical_significance":[],"seq_region_name":"7","id":"rs906410403","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506682,"feature_type":"variation","strand":1,"end":140506682,"alleles":["C","A"]},{"end":140506684,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140506684,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130425891","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506692,"feature_type":"variation","strand":1,"alleles":["G","C","T"],"end":140506692,"clinical_significance":[],"seq_region_name":"7","id":"rs1387275016"},{"seq_region_name":"7","id":"rs1182160579","clinical_significance":[],"start":140506695,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140506695,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1025643500","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506696,"source":"dbSNP","strand":1,"feature_type":"variation","end":140506696,"alleles":["C","T"]},{"id":"rs955678018","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506698,"source":"dbSNP","strand":1,"feature_type":"variation","end":140506698,"alleles":["C","G"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506703,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140506703,"clinical_significance":[],"seq_region_name":"7","id":"rs1008299504"},{"alleles":["G","A","T"],"end":140506704,"feature_type":"variation","strand":1,"source":"dbSNP","start":140506704,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs181786580"},{"source":"dbSNP","start":140506709,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140506709,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1056193273"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506722,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140506722,"seq_region_name":"7","id":"rs1194911538","clinical_significance":[]},{"end":140506726,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140506726,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795579709","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506735,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140506735,"seq_region_name":"7","id":"rs745759635","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs117505215","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506736,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140506736},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506737,"feature_type":"variation","strand":1,"end":140506737,"alleles":["T","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1243506290"},{"seq_region_name":"7","id":"rs1795579848","clinical_significance":[],"start":140506738,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140506738,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1381762710","seq_region_name":"7","source":"dbSNP","start":140506742,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140506742,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140506749,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506749,"source":"dbSNP","seq_region_name":"7","id":"rs1048440066","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1309962457","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140506750,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506750},{"seq_region_name":"7","id":"rs35855703","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506755,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","T"],"end":140506755},{"seq_region_name":"7","id":"rs1795580098","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C","T"],"end":140506760,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506760,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140506762,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506762,"source":"dbSNP","seq_region_name":"7","id":"rs1795580135","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795580174","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506762,"feature_type":"variation","strand":1,"alleles":["GTAACGGCTATGTAAA","GTAACGGCTATGTAAAGGGTAACGGCTATGTAAA"],"end":140506777},{"seq_region_name":"7","id":"rs1795580210","clinical_significance":[],"start":140506763,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140506763,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1334102263","seq_region_name":"7","feature_type":"variation","strand":1,"end":140506765,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506765},{"clinical_significance":[],"seq_region_name":"7","id":"rs1328312248","end":140506766,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140506766,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs150020933","clinical_significance":[],"start":140506767,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140506767,"alleles":["G","A","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1795580443","seq_region_name":"7","end":140506772,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140506772,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506773,"source":"dbSNP","strand":1,"feature_type":"variation","end":140506773,"alleles":["G","A"],"id":"rs1585524977","seq_region_name":"7","clinical_significance":[]},{"end":140506774,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140506774,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs762885497"},{"seq_region_name":"7","id":"rs1161828158","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506776,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140506776},{"start":140506777,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140506777,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1424498363","clinical_significance":[]},{"source":"dbSNP","start":140506778,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140506778,"alleles":["T","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs74421108","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs746757379","source":"dbSNP","start":140506779,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140506779,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140506790,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506790,"clinical_significance":[],"seq_region_name":"7","id":"rs1179510857"},{"start":140506793,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140506793,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs966009798","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795580708","seq_region_name":"7","alleles":["T","G"],"end":140506800,"feature_type":"variation","strand":1,"source":"dbSNP","start":140506800,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506803,"feature_type":"variation","strand":1,"alleles":["-","A"],"end":140506802,"clinical_significance":[],"seq_region_name":"7","id":"rs1795580789"},{"alleles":["G","T"],"end":140506803,"feature_type":"variation","strand":1,"source":"dbSNP","start":140506803,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795580817"},{"seq_region_name":"7","id":"rs1469024600","clinical_significance":[],"alleles":["T","-"],"end":140506804,"strand":1,"feature_type":"variation","start":140506804,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506808,"source":"dbSNP","strand":1,"feature_type":"variation","end":140506829,"alleles":["GCTCACACAGAGCTCACACAGA","GCTCACACAGA","GCTCACACAGAGCTCACACAGAGCTCACACAGA"],"id":"rs1180496848","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506809,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140506809,"id":"rs1795580976","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1490353854","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506810,"source":"dbSNP","strand":1,"feature_type":"variation","end":140506810,"alleles":["T","-"]},{"strand":1,"feature_type":"variation","end":140506816,"alleles":["CACACA","CACA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506811,"source":"dbSNP","seq_region_name":"7","id":"rs1795581053","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506813,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140506813,"clinical_significance":[],"seq_region_name":"7","id":"rs1293577133"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140506814,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506814,"source":"dbSNP","seq_region_name":"7","id":"rs1219782896","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1358528493","source":"dbSNP","start":140506815,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140506815,"feature_type":"variation","strand":1},{"end":140506819,"alleles":["AGAG","AG"],"strand":1,"feature_type":"variation","start":140506816,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795581189","clinical_significance":[]},{"end":140506818,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140506818,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1422173247","seq_region_name":"7"},{"start":140506822,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["CACACA","CACA"],"end":140506827,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795581253","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140506823,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506823,"clinical_significance":[],"id":"rs1286431923","seq_region_name":"7"},{"end":140506828,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140506828,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795581311","clinical_significance":[]},{"start":140506829,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140506829,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs996558765","clinical_significance":[]},{"clinical_significance":[],"id":"rs1348487370","seq_region_name":"7","alleles":["G","A"],"end":140506833,"feature_type":"variation","strand":1,"source":"dbSNP","start":140506833,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140506835,"alleles":["G","A","C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506835,"clinical_significance":[],"seq_region_name":"7","id":"rs967651283"},{"id":"rs112084318","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506836,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140506836},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506839,"source":"dbSNP","strand":1,"feature_type":"variation","end":140506839,"alleles":["G","A"],"id":"rs1795581434","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140506842,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506842,"source":"dbSNP","seq_region_name":"7","id":"rs1301584603","clinical_significance":[]},{"end":140506845,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140506845,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1404541852"},{"clinical_significance":[],"id":"rs1361617329","seq_region_name":"7","source":"dbSNP","start":140506846,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140506846,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs923615027","clinical_significance":[],"end":140506852,"alleles":["C","A","G"],"strand":1,"feature_type":"variation","start":140506852,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506855,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140506855,"seq_region_name":"7","id":"rs768509307","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130426047","alleles":["T","C"],"end":140506856,"feature_type":"variation","strand":1,"source":"dbSNP","start":140506856,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs989244681","source":"dbSNP","start":140506857,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140506857,"alleles":["A","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1407909722","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140506860,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506860,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795581684","source":"dbSNP","start":140506861,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140506861,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795581717","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506866,"feature_type":"variation","strand":1,"end":140506866,"alleles":["A","G"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506869,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140506869,"clinical_significance":[],"seq_region_name":"7","id":"rs1354236560"},{"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140506870,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506870,"source":"dbSNP","seq_region_name":"7","id":"rs776255791","clinical_significance":[]},{"seq_region_name":"7","id":"rs916302021","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140506872,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506872,"source":"dbSNP"},{"alleles":["C","G"],"end":140506874,"feature_type":"variation","strand":1,"source":"dbSNP","start":140506874,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1224832743"},{"alleles":["GG","G"],"end":140506877,"strand":1,"feature_type":"variation","start":140506876,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1270387985","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1255745870","clinical_significance":[],"strand":1,"feature_type":"variation","end":140506877,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506877,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140506880,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506880,"clinical_significance":[],"seq_region_name":"7","id":"rs1795581873"},{"seq_region_name":"7","id":"rs1795581901","clinical_significance":[],"start":140506883,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140506885,"alleles":["GGG","GG"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140506884,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506884,"clinical_significance":[],"seq_region_name":"7","id":"rs1196889449"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506885,"source":"dbSNP","strand":1,"feature_type":"variation","end":140506885,"alleles":["G","T"],"seq_region_name":"7","id":"rs62485798","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795582014","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506889,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140506889},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506890,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140506890,"clinical_significance":[],"seq_region_name":"7","id":"rs1795582040"},{"strand":1,"feature_type":"variation","end":140506898,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506898,"source":"dbSNP","seq_region_name":"7","id":"rs1242293846","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140506905,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506905,"source":"dbSNP","seq_region_name":"7","id":"rs1795582092","clinical_significance":[]},{"alleles":["C","G"],"end":140506911,"feature_type":"variation","strand":1,"source":"dbSNP","start":140506911,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795582115","seq_region_name":"7"},{"id":"rs2130426080","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140506912,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506912,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506915,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140506915,"seq_region_name":"7","id":"rs2130426087","clinical_significance":[]},{"seq_region_name":"7","id":"rs1271846002","clinical_significance":[],"start":140506916,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140506916,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140506918,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140506918,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1217696938"},{"start":140506920,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140506920,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795582169","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs115537853","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506927,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140506927},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506931,"source":"dbSNP","strand":1,"feature_type":"variation","end":140506931,"alleles":["C","A","T"],"seq_region_name":"7","id":"rs1283552755","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1219723271","source":"dbSNP","start":140506937,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140506937,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1795582258","seq_region_name":"7","source":"dbSNP","start":140506938,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140506938,"feature_type":"variation","strand":1},{"start":140506939,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["CAGTCAG","CAG"],"end":140506945,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585525049","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506940,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140506940,"clinical_significance":[],"seq_region_name":"7","id":"rs1795582290"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506941,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140506941,"clinical_significance":[],"seq_region_name":"7","id":"rs898447763"},{"source":"dbSNP","start":140506949,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140506949,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795582329"},{"clinical_significance":[],"seq_region_name":"7","id":"rs927901854","end":140506950,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140506950,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795582369","feature_type":"variation","strand":1,"end":140506957,"alleles":["AAG","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506955},{"id":"rs1795582391","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140506958,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506958,"source":"dbSNP"},{"id":"rs1281416595","seq_region_name":"7","clinical_significance":[],"start":140506961,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140506961,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1222937828","end":140506964,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140506964,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140506965,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140506965,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795582446","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140506966,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506966,"clinical_significance":[],"id":"rs769265591","seq_region_name":"7"},{"end":140506967,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140506967,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795582508","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","A"],"end":140506969,"strand":1,"feature_type":"variation","start":140506969,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1055822678","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140506970,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506970,"clinical_significance":[],"seq_region_name":"7","id":"rs1795582551"},{"seq_region_name":"7","id":"rs772741204","clinical_significance":[],"start":140506971,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140506971,"strand":1,"feature_type":"variation"},{"end":140506977,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140506977,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1348895994","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506981,"feature_type":"variation","strand":1,"end":140506981,"alleles":["T","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1344961382"},{"alleles":["T","A","C"],"end":140506983,"feature_type":"variation","strand":1,"source":"dbSNP","start":140506983,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs891112193"},{"id":"rs1427770541","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140506988,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506988,"source":"dbSNP"},{"id":"rs1018387100","seq_region_name":"7","clinical_significance":[],"start":140506990,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140506990,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140506995,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140506995,"source":"dbSNP","id":"rs1479793139","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130426138","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506997,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140506997},{"clinical_significance":[],"seq_region_name":"7","id":"rs1213257774","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140506998,"feature_type":"variation","strand":1,"end":140506998,"alleles":["G","A"]},{"alleles":["G","A"],"end":140507002,"strand":1,"feature_type":"variation","start":140507002,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1419799700","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507003,"feature_type":"variation","strand":1,"end":140507003,"alleles":["C","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs931300863"},{"clinical_significance":[],"seq_region_name":"7","id":"rs553541794","source":"dbSNP","start":140507004,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140507004,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795582783","source":"dbSNP","start":140507005,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140507005,"alleles":["C","A"],"feature_type":"variation","strand":1},{"id":"rs1484802158","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507007,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C","T"],"end":140507007},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130426154","source":"dbSNP","start":140507010,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140507010,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795582942","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507019,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140507019},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507022,"feature_type":"variation","strand":1,"end":140507022,"alleles":["T","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1241279311"},{"alleles":["C","T"],"end":140507023,"feature_type":"variation","strand":1,"source":"dbSNP","start":140507023,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1204266013"},{"seq_region_name":"7","id":"rs1462620355","clinical_significance":[],"start":140507027,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140507027,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs868583863","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140507029,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507029},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795583044","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507030,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140507030},{"seq_region_name":"7","id":"rs1261122647","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507036,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140507036},{"id":"rs1795583084","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140507038,"strand":1,"feature_type":"variation","start":140507038,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["A","C"],"end":140507042,"strand":1,"feature_type":"variation","start":140507042,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1011790603","clinical_significance":[]},{"id":"rs1795583199","seq_region_name":"7","clinical_significance":[],"start":140507045,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140507045,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507046,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140507046,"id":"rs1795583215","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507048,"source":"dbSNP","strand":1,"feature_type":"variation","end":140507048,"alleles":["G","T"],"seq_region_name":"7","id":"rs1195100925","clinical_significance":[]},{"clinical_significance":[],"id":"rs1298073735","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507050,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140507050},{"clinical_significance":[],"seq_region_name":"7","id":"rs1021792794","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507051,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140507051},{"clinical_significance":[],"seq_region_name":"7","id":"rs887152891","source":"dbSNP","start":140507056,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140507056,"alleles":["C","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1563108163","seq_region_name":"7","feature_type":"variation","strand":1,"end":140507064,"alleles":["GCTAACT","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507058},{"seq_region_name":"7","id":"rs1795583321","clinical_significance":[],"end":140507059,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140507059,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1244344008","source":"dbSNP","start":140507061,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140507061,"alleles":["A","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1285190772","clinical_significance":[],"strand":1,"feature_type":"variation","end":140507062,"alleles":["AA","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507061,"source":"dbSNP"},{"start":140507067,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140507067,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","id":"rs1585525096","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1004376105","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507068,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140507068},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507075,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140507075,"clinical_significance":[],"seq_region_name":"7","id":"rs1795583515"},{"clinical_significance":[],"id":"rs577296056","seq_region_name":"7","source":"dbSNP","start":140507077,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140507077,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795583569","source":"dbSNP","start":140507082,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140507082,"alleles":["C","G"],"feature_type":"variation","strand":1},{"start":140507083,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140507083,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795583586","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795583608","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140507086,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507086},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795583628","source":"dbSNP","start":140507088,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140507092,"alleles":["CCCCC","CCCC"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140507100,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507100,"source":"dbSNP","id":"rs901451671","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs997487112","clinical_significance":[],"start":140507102,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140507102,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1795583697","clinical_significance":[],"alleles":["C","T"],"end":140507108,"strand":1,"feature_type":"variation","start":140507108,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140507110,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140507110,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1028547868","clinical_significance":[]},{"clinical_significance":[],"id":"rs565733262","seq_region_name":"7","source":"dbSNP","start":140507113,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140507120,"alleles":["CCTCCCCC","CC"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs957952436","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507115,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140507115},{"seq_region_name":"7","id":"rs1795583744","clinical_significance":[],"start":140507116,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140507116,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["CCCCCC","CCCCCCC"],"end":140507121,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507116,"clinical_significance":[],"seq_region_name":"7","id":"rs960417007"},{"strand":1,"feature_type":"variation","end":140507117,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507117,"source":"dbSNP","seq_region_name":"7","id":"rs569585904","clinical_significance":[]},{"seq_region_name":"7","id":"rs545193683","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140507118,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507118,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs916333032","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507119,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140507119},{"seq_region_name":"7","id":"rs186908760","clinical_significance":[],"start":140507120,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","G","T"],"end":140507120,"strand":1,"feature_type":"variation"},{"id":"rs766851839","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","G"],"end":140507121,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507121,"source":"dbSNP"},{"start":140507121,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["CT","-"],"end":140507122,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1182906173","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1253119653","alleles":["T","C"],"end":140507122,"feature_type":"variation","strand":1,"source":"dbSNP","start":140507122,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1481028361","feature_type":"variation","strand":1,"end":140507122,"alleles":["T","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507122},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795583972","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507123,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140507123},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140507124,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507124,"source":"dbSNP","seq_region_name":"7","id":"rs919757180","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1307155957","feature_type":"variation","strand":1,"end":140507127,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507127},{"start":140507129,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140507129,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs865891277","clinical_significance":[]},{"start":140507135,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140507135,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs575716046","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795584070","clinical_significance":[],"alleles":["T","-"],"end":140507135,"strand":1,"feature_type":"variation","start":140507135,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140507137,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140507137,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1046995409"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795584114","feature_type":"variation","strand":1,"end":140507139,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507139},{"clinical_significance":[],"seq_region_name":"7","id":"rs1381027031","feature_type":"variation","strand":1,"end":140507141,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507141},{"seq_region_name":"7","id":"rs1795584158","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","-"],"end":140507151,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507151,"source":"dbSNP"},{"id":"rs1315041753","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140507154,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507154,"source":"dbSNP"},{"seq_region_name":"7","id":"rs891010258","clinical_significance":[],"start":140507159,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140507159,"alleles":["G","A","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1039688049","clinical_significance":[],"start":140507164,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140507164,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1459983439","source":"dbSNP","start":140507165,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140507165,"alleles":["G","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs899949937","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507167,"source":"dbSNP","strand":1,"feature_type":"variation","end":140507167,"alleles":["C","G"]},{"seq_region_name":"7","id":"rs981971736","clinical_significance":[],"start":140507168,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140507168,"strand":1,"feature_type":"variation"},{"start":140507169,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140507169,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795584306","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1022231873","feature_type":"variation","strand":1,"end":140507171,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507171},{"source":"dbSNP","start":140507175,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140507175,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1383130597"},{"id":"rs536932828","seq_region_name":"7","clinical_significance":[],"alleles":["A","G"],"end":140507177,"strand":1,"feature_type":"variation","start":140507177,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140507182,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507182,"clinical_significance":[],"seq_region_name":"7","id":"rs73735366"},{"seq_region_name":"7","id":"rs759974214","clinical_significance":[],"end":140507183,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140507183,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795584477","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507186,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140507186},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507188,"feature_type":"variation","strand":1,"end":140507188,"alleles":["C","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795584492"},{"feature_type":"variation","strand":1,"end":140507192,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507192,"clinical_significance":[],"seq_region_name":"7","id":"rs2130426311"},{"start":140507193,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140507193,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs372321326","clinical_significance":[]},{"end":140507195,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140507195,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795584526"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795584555","source":"dbSNP","start":140507198,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140507198,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs374505895","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140507199,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507199},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140507203,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507203,"source":"dbSNP","seq_region_name":"7","id":"rs1269949585","clinical_significance":[]},{"seq_region_name":"7","id":"rs991156822","clinical_significance":[],"alleles":["G","A"],"end":140507209,"strand":1,"feature_type":"variation","start":140507209,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140507216,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140507216,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1585525159","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs920489374","feature_type":"variation","strand":1,"end":140507224,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507224},{"strand":1,"feature_type":"variation","end":140507231,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507231,"source":"dbSNP","seq_region_name":"7","id":"rs1236849792","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507232,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140507232,"seq_region_name":"7","id":"rs1795584682","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507241,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140507241,"clinical_significance":[],"seq_region_name":"7","id":"rs115517940"},{"end":140507242,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140507242,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585525170","clinical_significance":[]},{"clinical_significance":[],"id":"rs1291465992","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507252,"feature_type":"variation","strand":1,"end":140507253,"alleles":["TT","TTT"]},{"end":140507260,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140507260,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs984082411","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1795584772","seq_region_name":"7","source":"dbSNP","start":140507261,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140507261,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507262,"feature_type":"variation","strand":1,"end":140507262,"alleles":["G","A","C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs559499816"},{"clinical_significance":[],"seq_region_name":"7","id":"rs940093615","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140507267,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507267},{"clinical_significance":[],"id":"rs991825268","seq_region_name":"7","end":140507268,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140507268,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1795584862","seq_region_name":"7","clinical_significance":[],"end":140507269,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140507269,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507270,"feature_type":"variation","strand":1,"alleles":["A","C","G","T"],"end":140507270,"clinical_significance":[],"seq_region_name":"7","id":"rs1795584880"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507272,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140507272,"clinical_significance":[],"id":"rs1585525184","seq_region_name":"7"},{"end":140507277,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140507277,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1286377227"},{"source":"dbSNP","start":140507278,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140507278,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1303441639","seq_region_name":"7"},{"alleles":["G","A"],"end":140507282,"strand":1,"feature_type":"variation","start":140507282,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795584975","clinical_significance":[]},{"seq_region_name":"7","id":"rs1023251268","clinical_significance":[],"start":140507285,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140507285,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"end":140507288,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140507288,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs969140208","clinical_significance":[]},{"end":140507290,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140507290,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130426372","clinical_significance":[]},{"id":"rs1198520625","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507295,"source":"dbSNP","strand":1,"feature_type":"variation","end":140507295,"alleles":["G","A","T"]},{"seq_region_name":"7","id":"rs1041218284","clinical_significance":[],"strand":1,"feature_type":"variation","end":140507299,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507299,"source":"dbSNP"},{"seq_region_name":"7","id":"rs533206530","clinical_significance":[],"start":140507302,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140507302,"alleles":["G","A","C","T"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507306,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140507306,"clinical_significance":[],"seq_region_name":"7","id":"rs1585525198"},{"alleles":["A","G"],"end":140507309,"strand":1,"feature_type":"variation","start":140507309,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1156829597","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507314,"feature_type":"variation","strand":1,"end":140507314,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795585163"},{"alleles":["G","C"],"end":140507317,"feature_type":"variation","strand":1,"source":"dbSNP","start":140507317,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1418632719"},{"id":"rs1215670831","seq_region_name":"7","clinical_significance":[],"start":140507318,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C"],"end":140507318,"strand":1,"feature_type":"variation"},{"alleles":["C","CC"],"end":140507322,"feature_type":"variation","strand":1,"source":"dbSNP","start":140507322,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs761630744","seq_region_name":"7"},{"source":"dbSNP","start":140507322,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140507322,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795585224"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507324,"source":"dbSNP","strand":1,"feature_type":"variation","end":140507324,"alleles":["G","A"],"id":"rs1489930898","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs919648787","feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140507331,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507331},{"seq_region_name":"7","id":"rs551589098","clinical_significance":[],"start":140507332,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140507332,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140507333,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140507333,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs114257959"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507335,"source":"dbSNP","strand":1,"feature_type":"variation","end":140507335,"alleles":["G","A"],"id":"rs1795585357","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs767255159","clinical_significance":[],"end":140507338,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140507338,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1192079663","end":140507339,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140507339,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795585418","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507340,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140507340},{"source":"dbSNP","start":140507341,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140507341,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2363820"},{"start":140507343,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140507343,"alleles":["A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1238944002","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507344,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140507344,"clinical_significance":[],"seq_region_name":"7","id":"rs894057138"},{"seq_region_name":"7","id":"rs549374651","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140507345,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507345,"source":"dbSNP"},{"end":140507350,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140507350,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795585566"},{"source":"dbSNP","start":140507351,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140507351,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1327911865"},{"feature_type":"variation","strand":1,"end":140507355,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507355,"clinical_significance":[],"seq_region_name":"7","id":"rs1439880982"},{"start":140507363,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140507363,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs755979945","clinical_significance":[]},{"start":140507368,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140507368,"strand":1,"feature_type":"variation","id":"rs752944540","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs567513510","feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140507369,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507369},{"clinical_significance":[],"id":"rs1795585724","seq_region_name":"7","end":140507371,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140507371,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795585744","source":"dbSNP","start":140507379,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140507379,"alleles":["G","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795585765","feature_type":"variation","strand":1,"end":140507380,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507380},{"feature_type":"variation","strand":1,"alleles":["T","TT"],"end":140507385,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507385,"clinical_significance":[],"seq_region_name":"7","id":"rs1795585786"},{"seq_region_name":"7","id":"rs1795585805","clinical_significance":[],"alleles":["G","C"],"end":140507386,"strand":1,"feature_type":"variation","start":140507386,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["G","A"],"end":140507387,"feature_type":"variation","strand":1,"source":"dbSNP","start":140507387,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1382635727"},{"seq_region_name":"7","id":"rs1386850446","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507388,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","G","T"],"end":140507388},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795585877","source":"dbSNP","start":140507389,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140507389,"alleles":["C","T"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507390,"feature_type":"variation","strand":1,"end":140507390,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795585909"},{"feature_type":"variation","strand":1,"end":140507392,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507392,"clinical_significance":[],"seq_region_name":"7","id":"rs902288427"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1287090184","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507395,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140507395},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795585981","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140507397,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507397},{"end":140507408,"alleles":["AAGATAAGA","AAGA"],"strand":1,"feature_type":"variation","start":140507400,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs576908749","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130426470","clinical_significance":[],"strand":1,"feature_type":"variation","end":140507405,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507405,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795586038","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["AA","-"],"end":140507406,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507405,"source":"dbSNP"},{"end":140507407,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140507407,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs947343953"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795586101","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507415,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140507415},{"clinical_significance":[],"id":"rs1795586125","seq_region_name":"7","alleles":["A","G"],"end":140507418,"feature_type":"variation","strand":1,"source":"dbSNP","start":140507418,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1178709678","clinical_significance":[],"end":140507420,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140507420,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["G","A","C"],"end":140507421,"strand":1,"feature_type":"variation","start":140507421,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1479465926","clinical_significance":[]},{"alleles":["T","C"],"end":140507424,"strand":1,"feature_type":"variation","start":140507424,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795586190","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs192187254","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140507425,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507425},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507426,"source":"dbSNP","strand":1,"feature_type":"variation","end":140507426,"alleles":["G","A","T"],"seq_region_name":"7","id":"rs1400084802","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585525244","source":"dbSNP","start":140507427,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140507427,"alleles":["C","G"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140507430,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140507430,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1428869219","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["AA","A"],"end":140507431,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507430,"source":"dbSNP","seq_region_name":"7","id":"rs1795586339","clinical_significance":[]},{"alleles":["G","T"],"end":140507432,"feature_type":"variation","strand":1,"source":"dbSNP","start":140507432,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795586360","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["C","A","G"],"end":140507434,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507434,"source":"dbSNP","id":"rs1795586388","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795586426","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507434,"feature_type":"variation","strand":1,"end":140507440,"alleles":["CTCCTCC","CTCC"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795586443","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507436,"feature_type":"variation","strand":1,"end":140507447,"alleles":["CCTCCCCTCCCC","CCTCCCC"]},{"seq_region_name":"7","id":"rs1043160187","clinical_significance":[],"end":140507437,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140507437,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1003312685","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507442,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140507442},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507445,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140507445,"id":"rs2130426516","seq_region_name":"7","clinical_significance":[]},{"id":"rs1430725412","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507446,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140507446},{"start":140507448,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140507448,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1034747915","clinical_significance":[]},{"seq_region_name":"7","id":"rs1462171585","clinical_significance":[],"end":140507451,"alleles":["GG","G"],"strand":1,"feature_type":"variation","start":140507450,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795586624","clinical_significance":[],"start":140507460,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140507460,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"alleles":["C","A"],"end":140507463,"feature_type":"variation","strand":1,"source":"dbSNP","start":140507463,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1265480208"},{"seq_region_name":"7","id":"rs1795586668","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507466,"source":"dbSNP","strand":1,"feature_type":"variation","end":140507466,"alleles":["T","C"]},{"id":"rs1795586687","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507468,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140507468},{"strand":1,"feature_type":"variation","end":140507472,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507472,"source":"dbSNP","seq_region_name":"7","id":"rs1795586710","clinical_significance":[]},{"seq_region_name":"7","id":"rs149199929","clinical_significance":[],"end":140507473,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140507473,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140507475,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140507475,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795586768"},{"end":140507477,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140507477,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1438454376"},{"end":140507479,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140507479,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795586834"},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140507480,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507480,"clinical_significance":[],"seq_region_name":"7","id":"rs577906410"},{"strand":1,"feature_type":"variation","end":140507483,"alleles":["T","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507483,"source":"dbSNP","id":"rs1795586859","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1028023269","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507489,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140507489},{"clinical_significance":[],"id":"rs1795586923","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140507493,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507493},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140507494,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507494,"source":"dbSNP","id":"rs1328026112","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507495,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140507495,"seq_region_name":"7","id":"rs1795586976","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140507497,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507497,"source":"dbSNP","seq_region_name":"7","id":"rs951955704","clinical_significance":[]},{"end":140507498,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140507498,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs183719965","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507501,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140507501,"seq_region_name":"7","id":"rs1795587080","clinical_significance":[]},{"start":140507504,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140507504,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130426593","clinical_significance":[]},{"seq_region_name":"7","id":"rs1338548814","clinical_significance":[],"start":140507508,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140507508,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140507513,"alleles":["A","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507513,"source":"dbSNP","seq_region_name":"7","id":"rs11972243","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1401569139","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507514,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140507514},{"id":"rs1795587207","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507521,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140507521},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585525302","source":"dbSNP","start":140507522,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140507522,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795587262","clinical_significance":[],"end":140507536,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140507536,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140507540,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140507540,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs969045369"},{"clinical_significance":[],"seq_region_name":"7","id":"rs557109632","source":"dbSNP","start":140507541,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140507541,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs56344848","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140507544,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507544,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs541467060","source":"dbSNP","start":140507548,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140507548,"alleles":["G","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1445544460","source":"dbSNP","start":140507549,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140507549,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507550,"feature_type":"variation","strand":1,"end":140507550,"alleles":["G","A"],"clinical_significance":[],"id":"rs561732372","seq_region_name":"7"},{"alleles":["GGAT","GGATGGAT"],"end":140507553,"strand":1,"feature_type":"variation","start":140507550,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795587580","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507557,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140507557,"seq_region_name":"7","id":"rs1795587617","clinical_significance":[]},{"seq_region_name":"7","id":"rs1182269048","clinical_significance":[],"strand":1,"feature_type":"variation","end":140507558,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507558,"source":"dbSNP"},{"id":"rs1763486831","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507559,"source":"dbSNP","strand":1,"feature_type":"variation","end":140507559,"alleles":["G","A"]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140507561,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507561,"source":"dbSNP","seq_region_name":"7","id":"rs1274369321","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507562,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140507562,"clinical_significance":[],"id":"rs146867326","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507563,"feature_type":"variation","strand":1,"end":140507563,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795587757"},{"clinical_significance":[],"id":"rs559767973","seq_region_name":"7","feature_type":"variation","strand":1,"end":140507564,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507564},{"id":"rs1249203458","seq_region_name":"7","clinical_significance":[],"end":140507569,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140507569,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140507575,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507575,"source":"dbSNP","seq_region_name":"7","id":"rs1049917067","clinical_significance":[]},{"clinical_significance":[],"id":"rs1383255707","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140507577,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507577},{"feature_type":"variation","strand":1,"end":140507578,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507578,"clinical_significance":[],"seq_region_name":"7","id":"rs912370547"},{"strand":1,"feature_type":"variation","end":140507580,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507580,"source":"dbSNP","seq_region_name":"7","id":"rs1795587907","clinical_significance":[]},{"seq_region_name":"7","id":"rs1450330473","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140507584,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507584,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507585,"feature_type":"variation","strand":1,"end":140507585,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1339987537"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795587993","source":"dbSNP","start":140507586,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140507586,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs965311050","source":"dbSNP","start":140507589,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140507589,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1393153920","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140507591,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507591},{"id":"rs1394610616","seq_region_name":"7","clinical_significance":[],"start":140507592,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140507592,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"end":140507600,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140507600,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1438095442","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs559425351","clinical_significance":[],"end":140507604,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140507604,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs975343312","seq_region_name":"7","source":"dbSNP","start":140507610,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140507610,"alleles":["A","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs921151176","clinical_significance":[],"start":140507619,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140507619,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140507625,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507625,"source":"dbSNP","seq_region_name":"7","id":"rs1795588270","clinical_significance":[]},{"clinical_significance":[],"id":"rs1163272207","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507629,"feature_type":"variation","strand":1,"end":140507629,"alleles":["T","G"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507631,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140507631,"seq_region_name":"7","id":"rs11972270","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795588349","feature_type":"variation","strand":1,"end":140507634,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507634},{"seq_region_name":"7","id":"rs753903341","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507637,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140507637},{"id":"rs1459769784","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507638,"source":"dbSNP","strand":1,"feature_type":"variation","end":140507638,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1042640522","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507641,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140507641},{"start":140507642,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140507642,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1203986697","clinical_significance":[]},{"clinical_significance":[],"id":"rs1359949892","seq_region_name":"7","source":"dbSNP","start":140507644,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140507644,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795588529","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140507646,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507646},{"end":140507647,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140507647,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs902195435","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs778085553","feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140507648,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507648},{"clinical_significance":[],"seq_region_name":"7","id":"rs1355573154","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507651,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140507651},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795588640","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507653,"feature_type":"variation","strand":1,"end":140507653,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs947377757","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507654,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140507654},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140507655,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507655,"source":"dbSNP","seq_region_name":"7","id":"rs1795588715","clinical_significance":[]},{"clinical_significance":[],"id":"rs1585525391","seq_region_name":"7","feature_type":"variation","strand":1,"end":140507661,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507661},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507665,"source":"dbSNP","strand":1,"feature_type":"variation","end":140507665,"alleles":["T","G"],"seq_region_name":"7","id":"rs1334040097","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795588790","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507669,"source":"dbSNP","strand":1,"feature_type":"variation","end":140507669,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1331118469","alleles":["G","A","C"],"end":140507670,"feature_type":"variation","strand":1,"source":"dbSNP","start":140507670,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507675,"source":"dbSNP","strand":1,"feature_type":"variation","end":140507675,"alleles":["G","T"],"seq_region_name":"7","id":"rs747178195","clinical_significance":[]},{"clinical_significance":[],"id":"rs533245396","seq_region_name":"7","source":"dbSNP","start":140507681,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140507681,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507683,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140507683,"seq_region_name":"7","id":"rs1795588929","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs757293554","source":"dbSNP","start":140507687,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140507687,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs924758727","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507690,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140507690},{"clinical_significance":[],"seq_region_name":"7","id":"rs551626309","source":"dbSNP","start":140507691,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140507691,"feature_type":"variation","strand":1},{"start":140507692,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140507692,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs894891837","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140507693,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507693,"clinical_significance":[],"seq_region_name":"7","id":"rs1795589067"},{"clinical_significance":[],"id":"rs1795589089","seq_region_name":"7","source":"dbSNP","start":140507694,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140507694,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507695,"feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140507695,"clinical_significance":[],"seq_region_name":"7","id":"rs1057330839"},{"start":140507699,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140507699,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1441569631","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507700,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140507700,"seq_region_name":"7","id":"rs1795589196","clinical_significance":[]},{"seq_region_name":"7","id":"rs186494933","clinical_significance":[],"start":140507701,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140507701,"alleles":["C","A","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs531036486","alleles":["G","A","T"],"end":140507702,"feature_type":"variation","strand":1,"source":"dbSNP","start":140507702,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs899392902","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507709,"source":"dbSNP","strand":1,"feature_type":"variation","end":140507709,"alleles":["A","G"]},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140507716,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507716,"source":"dbSNP","seq_region_name":"7","id":"rs1795589292","clinical_significance":[]},{"start":140507724,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140507724,"alleles":["C","A"],"strand":1,"feature_type":"variation","id":"rs1219115110","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs549163421","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507729,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140507729},{"alleles":["C","A"],"end":140507732,"strand":1,"feature_type":"variation","start":140507732,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130426781","clinical_significance":[]},{"seq_region_name":"7","id":"rs1027065989","clinical_significance":[],"start":140507734,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140507734,"alleles":["G","A","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1340492324","alleles":["G","T"],"end":140507740,"feature_type":"variation","strand":1,"source":"dbSNP","start":140507740,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795589604","clinical_significance":[],"strand":1,"feature_type":"variation","end":140507742,"alleles":["A","C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507742,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140507746,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507746,"clinical_significance":[],"id":"rs983349304","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1014763819","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507754,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140507754},{"clinical_significance":[],"id":"rs961363302","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507755,"feature_type":"variation","strand":1,"end":140507755,"alleles":["T","C"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507757,"source":"dbSNP","strand":1,"feature_type":"variation","end":140507757,"alleles":["A","G"],"id":"rs1004349506","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1019348401","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507760,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140507760},{"id":"rs1347640414","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140507763,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507763,"source":"dbSNP"},{"id":"rs1281542756","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507766,"source":"dbSNP","strand":1,"feature_type":"variation","end":140507766,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585525433","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507769,"feature_type":"variation","strand":1,"end":140507769,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs965218596","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140507772,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507772},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507773,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140507773,"clinical_significance":[],"seq_region_name":"7","id":"rs1795589904"},{"strand":1,"feature_type":"variation","end":140507776,"alleles":["TCTC","TC"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507773,"source":"dbSNP","seq_region_name":"7","id":"rs1346146746","clinical_significance":[]},{"seq_region_name":"7","id":"rs567746014","clinical_significance":[],"alleles":["C","A","T"],"end":140507774,"strand":1,"feature_type":"variation","start":140507774,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140507775,"alleles":["T","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507775,"clinical_significance":[],"seq_region_name":"7","id":"rs1795589992"},{"id":"rs1795590011","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140507777,"alleles":["TCA","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507775,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140507776,"alleles":["C","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507776,"source":"dbSNP","seq_region_name":"7","id":"rs1320912408","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1480439793","end":140507776,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140507776,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140507776,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140507777,"alleles":["CA","-"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1491231915","clinical_significance":[]},{"seq_region_name":"7","id":"rs1388498007","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507776,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CAA","-"],"end":140507778},{"feature_type":"variation","strand":1,"end":140507779,"alleles":["CAAA","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507776,"clinical_significance":[],"seq_region_name":"7","id":"rs1157789135"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507777,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140507777,"clinical_significance":[],"seq_region_name":"7","id":"rs1795590140"},{"seq_region_name":"7","id":"rs66945646","clinical_significance":[],"start":140507777,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAA"],"end":140507799,"strand":1,"feature_type":"variation"},{"end":140507778,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140507778,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1436793832"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1188079377","end":140507779,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140507779,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795590349","clinical_significance":[],"start":140507780,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140507780,"alleles":["A","C","G"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140507782,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140507782,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795590363"},{"clinical_significance":[],"id":"rs1585525455","seq_region_name":"7","source":"dbSNP","start":140507783,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140507783,"alleles":["A","G"],"feature_type":"variation","strand":1},{"end":140507786,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140507786,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1258983324"},{"seq_region_name":"7","id":"rs2130426901","clinical_significance":[],"strand":1,"feature_type":"variation","end":140507790,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507790,"source":"dbSNP"},{"end":140507793,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140507793,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795590421"},{"start":140507794,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140507801,"alleles":["AAAAAAGA","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795590437","clinical_significance":[]},{"start":140507795,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140507795,"alleles":["A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1204394865","clinical_significance":[]},{"end":140507801,"alleles":["AAAAGA","A"],"strand":1,"feature_type":"variation","start":140507796,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1325759170","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1474211021","alleles":["AAAGA","A"],"end":140507801,"feature_type":"variation","strand":1,"source":"dbSNP","start":140507797,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1164126423","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507798,"feature_type":"variation","strand":1,"end":140507801,"alleles":["AAGA","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1272321584","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507799,"feature_type":"variation","strand":1,"end":140507799,"alleles":["A","T"]},{"clinical_significance":[],"id":"rs869061700","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507799,"feature_type":"variation","strand":1,"alleles":["AGA","A"],"end":140507801},{"feature_type":"variation","strand":1,"end":140507800,"alleles":["G","A","C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507800,"clinical_significance":[],"seq_region_name":"7","id":"rs11982560"},{"id":"rs1429002573","seq_region_name":"7","clinical_significance":[],"alleles":["G","-"],"end":140507800,"strand":1,"feature_type":"variation","start":140507800,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795590619","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507801,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140507801},{"seq_region_name":"7","id":"rs1795590646","clinical_significance":[],"alleles":["AT","-"],"end":140507802,"strand":1,"feature_type":"variation","start":140507801,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507802,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","G"],"end":140507802,"seq_region_name":"7","id":"rs1165872560","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130426940","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507802,"feature_type":"variation","strand":1,"alleles":["T","-"],"end":140507802},{"clinical_significance":[],"id":"rs1394644702","seq_region_name":"7","source":"dbSNP","start":140507806,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140507806,"alleles":["A","G","T"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140507807,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507807,"source":"dbSNP","id":"rs1469918480","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130426948","source":"dbSNP","start":140507808,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140507808,"feature_type":"variation","strand":1},{"start":140507809,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140507809,"alleles":["T","A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130426949","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507813,"source":"dbSNP","strand":1,"feature_type":"variation","end":140507812,"alleles":["-","ATGCCA"],"seq_region_name":"7","id":"rs1795590789","clinical_significance":[]},{"id":"rs1585525484","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140507813,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507813,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1407626657","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507816,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140507816},{"id":"rs1585525488","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140507817,"strand":1,"feature_type":"variation","start":140507817,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795590884","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507818,"feature_type":"variation","strand":1,"end":140507817,"alleles":["-","ATAACATGTCCATGCCA"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507819,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140507819,"clinical_significance":[],"id":"rs1173566535","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507822,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140507822,"seq_region_name":"7","id":"rs1585525491","clinical_significance":[]},{"end":140507823,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140507823,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs975210091","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1419725517","source":"dbSNP","start":140507824,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A","G"],"end":140507824,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507826,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140507826,"clinical_significance":[],"id":"rs1795591032","seq_region_name":"7"},{"end":140507827,"alleles":["C","A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140507827,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1447369255"},{"feature_type":"variation","strand":1,"end":140507829,"alleles":["T","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507829,"clinical_significance":[],"seq_region_name":"7","id":"rs1585525497"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140507833,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507833,"source":"dbSNP","seq_region_name":"7","id":"rs1585525500","clinical_significance":[]},{"clinical_significance":[],"id":"rs1247419592","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507834,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140507834},{"id":"rs1184119424","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507835,"source":"dbSNP","strand":1,"feature_type":"variation","end":140507835,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1462751078","alleles":["A","G","T"],"end":140507839,"feature_type":"variation","strand":1,"source":"dbSNP","start":140507839,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795591247","feature_type":"variation","strand":1,"end":140507840,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507840},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507844,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140507844,"id":"rs1795591279","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1209458427","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507845,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140507845},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795591324","source":"dbSNP","start":140507845,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["ACT","-"],"end":140507847,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["C","-"],"end":140507846,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507846,"source":"dbSNP","seq_region_name":"7","id":"rs1795591344","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507846,"feature_type":"variation","strand":1,"alleles":["CTT","-"],"end":140507848,"clinical_significance":[],"seq_region_name":"7","id":"rs1308326101"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507846,"feature_type":"variation","strand":1,"end":140507849,"alleles":["CTTT","-"],"clinical_significance":[],"seq_region_name":"7","id":"rs1275297930"},{"seq_region_name":"7","id":"rs1409556362","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507847,"source":"dbSNP","strand":1,"feature_type":"variation","end":140507847,"alleles":["T","C"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507847,"source":"dbSNP","strand":1,"feature_type":"variation","end":140507866,"alleles":["TTTTTTTTTTTTTTTTTTTT","TTTTTTTTTT","TTTTTTTTTTT","TTTTTTTTTTTTTT","TTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTT"],"seq_region_name":"7","id":"rs138504258","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507849,"feature_type":"variation","strand":1,"end":140507849,"alleles":["T","C"],"clinical_significance":[],"id":"rs1795591668","seq_region_name":"7"},{"start":140507850,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140507850,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795591688","clinical_significance":[]},{"seq_region_name":"7","id":"rs1172089414","clinical_significance":[],"start":140507854,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140507854,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795591752","end":140507859,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140507859,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507860,"feature_type":"variation","strand":1,"end":140507860,"alleles":["T","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1427651599"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1313611551","source":"dbSNP","start":140507864,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140507867,"alleles":["TTTG","-"],"feature_type":"variation","strand":1},{"start":140507865,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140507867,"alleles":["TTG","-"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1357412475","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507866,"source":"dbSNP","strand":1,"feature_type":"variation","end":140507866,"alleles":["T","G"],"seq_region_name":"7","id":"rs1480997236","clinical_significance":[]},{"source":"dbSNP","start":140507866,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140507867,"alleles":["TG","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1446404683"},{"id":"rs1253937921","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["TGA","-"],"end":140507868,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507866,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507866,"feature_type":"variation","strand":1,"end":140507869,"alleles":["TGAA","-"],"clinical_significance":[],"id":"rs1399031326","seq_region_name":"7"},{"source":"dbSNP","start":140507867,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140507867,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs73735367"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1234870644","feature_type":"variation","strand":1,"end":140507867,"alleles":["G","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507867},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507867,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GA","-"],"end":140507868,"id":"rs1795592075","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1203257259","alleles":["GAAGA","GA"],"end":140507871,"feature_type":"variation","strand":1,"source":"dbSNP","start":140507867,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1585525560","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["AA","A"],"end":140507869,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507868,"source":"dbSNP"},{"source":"dbSNP","start":140507869,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140507869,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795592155"},{"end":140507870,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140507870,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795592176"},{"feature_type":"variation","strand":1,"end":140507873,"alleles":["TT","TTTT","TTTTTTTTTGTTTTTTTTTTTTT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507872,"clinical_significance":[],"seq_region_name":"7","id":"rs1293197978"},{"source":"dbSNP","start":140507874,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140507874,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1028555292"},{"end":140507876,"alleles":["G","C","T"],"strand":1,"feature_type":"variation","start":140507876,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1249931317","clinical_significance":[]},{"end":140507877,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140507877,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1338365371"},{"clinical_significance":[],"id":"rs1248554781","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140507878,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507878},{"clinical_significance":[],"id":"rs1320453215","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507883,"feature_type":"variation","strand":1,"end":140507883,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs968718237","clinical_significance":[],"strand":1,"feature_type":"variation","end":140507884,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507884,"source":"dbSNP"},{"alleles":["A","G"],"end":140507887,"feature_type":"variation","strand":1,"source":"dbSNP","start":140507887,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795592423"},{"end":140507888,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140507888,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1281931978"},{"source":"dbSNP","start":140507890,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140507890,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795592485"},{"id":"rs921183946","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140507893,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507893,"source":"dbSNP"},{"source":"dbSNP","start":140507894,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","G","T"],"end":140507894,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs7783408"},{"alleles":["G","A"],"end":140507895,"feature_type":"variation","strand":1,"source":"dbSNP","start":140507895,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs922715303"},{"start":140507896,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140507896,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795592691","clinical_significance":[]},{"clinical_significance":[],"id":"rs954143946","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507898,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140507898},{"end":140507900,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140507900,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795592714","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs986056125","feature_type":"variation","strand":1,"end":140507903,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507903},{"clinical_significance":[],"id":"rs1303560889","seq_region_name":"7","source":"dbSNP","start":140507905,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140507905,"alleles":["A","G"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140507909,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507909,"source":"dbSNP","seq_region_name":"7","id":"rs1795592768","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795592783","clinical_significance":[],"end":140507911,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140507911,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507913,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140507913,"seq_region_name":"7","id":"rs1426255839","clinical_significance":[]},{"source":"dbSNP","start":140507914,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140507914,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs915431117"},{"seq_region_name":"7","id":"rs1795592838","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507918,"source":"dbSNP","strand":1,"feature_type":"variation","end":140507918,"alleles":["C","G"]},{"start":140507922,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140507922,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs116619132","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585525610","clinical_significance":[],"alleles":["T","G"],"end":140507925,"strand":1,"feature_type":"variation","start":140507925,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795592899","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507927,"source":"dbSNP","strand":1,"feature_type":"variation","end":140507927,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs924594216","source":"dbSNP","start":140507933,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140507933,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795592947","clinical_significance":[],"start":140507936,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140507936,"strand":1,"feature_type":"variation"},{"start":140507941,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140507941,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795592974","clinical_significance":[]},{"seq_region_name":"7","id":"rs934786746","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507943,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140507943},{"seq_region_name":"7","id":"rs571634891","clinical_significance":[],"end":140507947,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140507947,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507951,"source":"dbSNP","strand":1,"feature_type":"variation","end":140507951,"alleles":["C","T"],"seq_region_name":"7","id":"rs1795593039","clinical_significance":[]},{"clinical_significance":[],"id":"rs1057467279","seq_region_name":"7","source":"dbSNP","start":140507953,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140507953,"feature_type":"variation","strand":1},{"start":140507956,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140507956,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1225189884","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507974,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140507974,"clinical_significance":[],"seq_region_name":"7","id":"rs1042671131"},{"source":"dbSNP","start":140507975,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140507975,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795593120"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507976,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140507976,"clinical_significance":[],"seq_region_name":"7","id":"rs1430196620"},{"clinical_significance":[],"seq_region_name":"7","id":"rs924150189","source":"dbSNP","start":140507977,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140507977,"alleles":["A","G"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507978,"feature_type":"variation","strand":1,"end":140507978,"alleles":["T","G"],"clinical_significance":[],"id":"rs1795593186","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140507982,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507982,"clinical_significance":[],"seq_region_name":"7","id":"rs542032288"},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140507983,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140507983,"clinical_significance":[],"id":"rs1585525632","seq_region_name":"7"},{"end":140507985,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140507985,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1056124895"},{"start":140507987,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140507987,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795593270","clinical_significance":[]},{"alleles":["C","T"],"end":140507989,"feature_type":"variation","strand":1,"source":"dbSNP","start":140507989,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1225988195"},{"seq_region_name":"7","id":"rs1044506612","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507990,"source":"dbSNP","strand":1,"feature_type":"variation","end":140507990,"alleles":["A","C"]},{"seq_region_name":"7","id":"rs899465162","clinical_significance":[],"strand":1,"feature_type":"variation","end":140507992,"alleles":["A","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140507992,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795593348","source":"dbSNP","start":140507996,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140508001,"alleles":["AAGAAG","AAG"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs768420970","clinical_significance":[],"end":140507997,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140507997,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795593398","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508001,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140508001},{"strand":1,"feature_type":"variation","end":140508008,"alleles":["T","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508008,"source":"dbSNP","seq_region_name":"7","id":"rs1292908201","clinical_significance":[]},{"alleles":["C","G","T"],"end":140508011,"feature_type":"variation","strand":1,"source":"dbSNP","start":140508011,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1174490156"},{"alleles":["C","G"],"end":140508015,"strand":1,"feature_type":"variation","start":140508015,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795593452","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140508017,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508017,"clinical_significance":[],"seq_region_name":"7","id":"rs1795593465"},{"feature_type":"variation","strand":1,"alleles":["T","A","G"],"end":140508027,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508027,"clinical_significance":[],"seq_region_name":"7","id":"rs1377413030"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795593499","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508028,"feature_type":"variation","strand":1,"end":140508028,"alleles":["A","G"]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140508032,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508032,"clinical_significance":[],"id":"rs189702127","seq_region_name":"7"},{"id":"rs71543376","seq_region_name":"7","clinical_significance":[],"end":140508040,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140508040,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1157045805","clinical_significance":[],"alleles":["A","C"],"end":140508041,"strand":1,"feature_type":"variation","start":140508041,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs563988802","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508046,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140508046},{"end":140508048,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140508048,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795593666","seq_region_name":"7"},{"end":140508051,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140508051,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs557148151","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1472266164","clinical_significance":[],"strand":1,"feature_type":"variation","end":140508056,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508056,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1430323155","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508063,"source":"dbSNP","strand":1,"feature_type":"variation","end":140508063,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1048080529","source":"dbSNP","start":140508064,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140508064,"alleles":["G","A","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1431852852","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508072,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140508072},{"source":"dbSNP","start":140508073,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140508073,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1386347267"},{"source":"dbSNP","start":140508075,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140508075,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1384366702"},{"alleles":["G","A"],"end":140508079,"strand":1,"feature_type":"variation","start":140508079,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1487150189","clinical_significance":[]},{"id":"rs1293933830","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508082,"source":"dbSNP","strand":1,"feature_type":"variation","end":140508082,"alleles":["G","A"]},{"end":140508083,"alleles":["GG","G"],"strand":1,"feature_type":"variation","start":140508082,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795593860","clinical_significance":[]},{"source":"dbSNP","start":140508083,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C","T"],"end":140508083,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795593880","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140508084,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508084,"clinical_significance":[],"seq_region_name":"7","id":"rs1326207865"},{"id":"rs1795593926","seq_region_name":"7","clinical_significance":[],"alleles":["A","G"],"end":140508086,"strand":1,"feature_type":"variation","start":140508086,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795593939","clinical_significance":[],"end":140508087,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140508087,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140508090,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140508090,"strand":1,"feature_type":"variation","id":"rs886791765","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795594377","clinical_significance":[],"strand":1,"feature_type":"variation","end":140508091,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508091,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1327849659","clinical_significance":[],"start":140508092,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140508092,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"id":"rs1795594424","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140508093,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508093,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1011978146","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140508095,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508095,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1003851676","source":"dbSNP","start":140508100,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140508100,"alleles":["C","T"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140508102,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508102,"source":"dbSNP","seq_region_name":"7","id":"rs1019380817","clinical_significance":[]},{"alleles":["G","A"],"end":140508103,"strand":1,"feature_type":"variation","start":140508103,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs11772142","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795594576","source":"dbSNP","start":140508105,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140508105,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140508112,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508112,"source":"dbSNP","id":"rs1328956548","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1209571621","source":"dbSNP","start":140508113,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140508113,"alleles":["A","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795594638","clinical_significance":[],"start":140508116,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140508116,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508117,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140508117,"clinical_significance":[],"seq_region_name":"7","id":"rs747970345"},{"alleles":["C","T"],"end":140508118,"strand":1,"feature_type":"variation","start":140508118,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1382513610","clinical_significance":[]},{"seq_region_name":"7","id":"rs996721897","clinical_significance":[],"start":140508120,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G","T"],"end":140508120,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140508123,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508123,"clinical_significance":[],"id":"rs887623411","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508127,"feature_type":"variation","strand":1,"end":140508127,"alleles":["C","T"],"clinical_significance":[],"id":"rs1585525686","seq_region_name":"7"},{"id":"rs968691369","seq_region_name":"7","clinical_significance":[],"end":140508128,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140508128,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795594926","alleles":["A","C"],"end":140508129,"feature_type":"variation","strand":1,"source":"dbSNP","start":140508129,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1203278317","end":140508130,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140508130,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140508132,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508132,"clinical_significance":[],"seq_region_name":"7","id":"rs1174579236"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795595000","alleles":["AGAGAG","AGAG"],"end":140508140,"feature_type":"variation","strand":1,"source":"dbSNP","start":140508135,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508137,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140508137,"clinical_significance":[],"seq_region_name":"7","id":"rs1795595028"},{"seq_region_name":"7","id":"rs1004636368","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140508140,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508140,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508142,"feature_type":"variation","strand":1,"end":140508142,"alleles":["T","G"],"clinical_significance":[],"id":"rs1795595083","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1795595107","seq_region_name":"7","source":"dbSNP","start":140508143,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140508143,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795595136","clinical_significance":[],"end":140508152,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140508152,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140508155,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508155,"clinical_significance":[],"seq_region_name":"7","id":"rs2130427294"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508156,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140508156,"clinical_significance":[],"seq_region_name":"7","id":"rs1014835628"},{"start":140508159,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140508159,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795595173","clinical_significance":[]},{"id":"rs1260861638","seq_region_name":"7","clinical_significance":[],"start":140508161,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140508161,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"alleles":["A","G"],"end":140508166,"strand":1,"feature_type":"variation","start":140508166,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795595227","seq_region_name":"7","clinical_significance":[]},{"start":140508167,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140508167,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795595256","clinical_significance":[]},{"end":140508171,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140508171,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1454538210","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs965929218","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140508176,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508176,"source":"dbSNP"},{"id":"rs116031901","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140508177,"strand":1,"feature_type":"variation","start":140508177,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140508178,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508178,"clinical_significance":[],"seq_region_name":"7","id":"rs537152178"},{"end":140508179,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140508179,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795595474"},{"end":140508182,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140508182,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs992754398","seq_region_name":"7","clinical_significance":[]},{"end":140508184,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140508184,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585525710"},{"start":140508185,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140508185,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1188459649","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795595582","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508186,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140508186},{"seq_region_name":"7","id":"rs1464079865","clinical_significance":[],"start":140508187,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140508187,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140508190,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140508190,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1175475542"},{"alleles":["T","C"],"end":140508191,"feature_type":"variation","strand":1,"source":"dbSNP","start":140508191,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1364430565"},{"source":"dbSNP","start":140508192,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140508192,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs954159995","seq_region_name":"7"},{"start":140508195,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140508195,"alleles":["C","A"],"strand":1,"feature_type":"variation","id":"rs1585525723","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1342448022","clinical_significance":[],"start":140508196,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G","T"],"end":140508196,"strand":1,"feature_type":"variation"},{"end":140508197,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140508197,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs985577075"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795595816","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508200,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140508200},{"start":140508201,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140508201,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1254979028","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795595878","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508207,"feature_type":"variation","strand":1,"end":140508207,"alleles":["C","T"]},{"feature_type":"variation","strand":1,"end":140508209,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508209,"clinical_significance":[],"seq_region_name":"7","id":"rs1795595907"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508215,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140508215,"id":"rs555215216","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795595974","source":"dbSNP","start":140508217,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140508217,"alleles":["T","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795596007","source":"dbSNP","start":140508218,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140508218,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140508221,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508221,"clinical_significance":[],"seq_region_name":"7","id":"rs1795596026"},{"id":"rs1287621019","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508222,"source":"dbSNP","strand":1,"feature_type":"variation","end":140508222,"alleles":["G","A","T"]},{"source":"dbSNP","start":140508223,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140508223,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795596115","seq_region_name":"7"},{"seq_region_name":"7","id":"rs948805221","clinical_significance":[],"strand":1,"feature_type":"variation","end":140508228,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508228,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1388478962","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508231,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140508231},{"clinical_significance":[],"id":"rs1795596209","seq_region_name":"7","end":140508237,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140508237,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140508242,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A","C"],"end":140508242,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1434243887","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1336275173","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508245,"feature_type":"variation","strand":1,"end":140508245,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1394306406","source":"dbSNP","start":140508246,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140508246,"alleles":["C","A"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140508251,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508251,"source":"dbSNP","seq_region_name":"7","id":"rs915295863","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140508255,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508255,"source":"dbSNP","seq_region_name":"7","id":"rs1795596355","clinical_significance":[]},{"id":"rs1795596381","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140508257,"alleles":["CCC","CC"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508255,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["AAA","AA"],"end":140508260,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508258,"source":"dbSNP","seq_region_name":"7","id":"rs980274938","clinical_significance":[]},{"source":"dbSNP","start":140508261,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140508261,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795596458"},{"seq_region_name":"7","id":"rs573668099","clinical_significance":[],"start":140508262,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140508262,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs978252612","end":140508263,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140508263,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140508268,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140508268,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795596562"},{"seq_region_name":"7","id":"rs1442109865","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508269,"source":"dbSNP","strand":1,"feature_type":"variation","end":140508272,"alleles":["TTTT","-"]},{"id":"rs1388672047","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508280,"source":"dbSNP","strand":1,"feature_type":"variation","end":140508280,"alleles":["T","C"]},{"strand":1,"feature_type":"variation","end":140508282,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508282,"source":"dbSNP","seq_region_name":"7","id":"rs1795596662","clinical_significance":[]},{"source":"dbSNP","start":140508286,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140508286,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs920742633"},{"start":140508287,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140508287,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795596718","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508292,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140508292,"seq_region_name":"7","id":"rs1445789679","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585525763","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508294,"feature_type":"variation","strand":1,"end":140508294,"alleles":["C","G"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508298,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","C","G"],"end":140508298,"seq_region_name":"7","id":"rs182316202","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130427408","clinical_significance":[],"end":140508305,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140508305,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140508314,"alleles":["CTTCTT","CTT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508309,"source":"dbSNP","seq_region_name":"7","id":"rs1189019524","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140508314,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508314,"clinical_significance":[],"seq_region_name":"7","id":"rs1585525770"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508317,"feature_type":"variation","strand":1,"end":140508317,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs939605845"},{"clinical_significance":[],"id":"rs1440188873","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140508324,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508324},{"start":140508332,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140508332,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1224763698","clinical_significance":[]},{"clinical_significance":[],"id":"rs1195999846","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140508334,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508334},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140508337,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508337,"source":"dbSNP","seq_region_name":"7","id":"rs1056555651","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140508341,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508341,"clinical_significance":[],"id":"rs373409460","seq_region_name":"7"},{"source":"dbSNP","start":140508346,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140508346,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795597089"},{"start":140508348,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140508348,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs1795597113","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs144563448","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508350,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140508350},{"seq_region_name":"7","id":"rs1227338466","clinical_significance":[],"strand":1,"feature_type":"variation","end":140508365,"alleles":["T","A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508365,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1285815646","source":"dbSNP","start":140508366,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140508366,"alleles":["T","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs886657006","clinical_significance":[],"alleles":["T","C"],"end":140508373,"strand":1,"feature_type":"variation","start":140508373,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs939684781","end":140508376,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140508376,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1048803876","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508377,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140508377},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508378,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140508378,"clinical_significance":[],"seq_region_name":"7","id":"rs1585525803"},{"seq_region_name":"7","id":"rs1795600992","clinical_significance":[],"start":140508379,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140508379,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"end":140508383,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140508383,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs887527898"},{"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140508384,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508384,"source":"dbSNP","seq_region_name":"7","id":"rs576040001","clinical_significance":[]},{"seq_region_name":"7","id":"rs1036143259","clinical_significance":[],"strand":1,"feature_type":"variation","end":140508385,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508385,"source":"dbSNP"},{"source":"dbSNP","start":140508391,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140508391,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130427451"},{"source":"dbSNP","start":140508393,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140508393,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1425613767"},{"start":140508396,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140508396,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795601153","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508399,"feature_type":"variation","strand":1,"end":140508399,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1416667616"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795601195","end":140508400,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140508400,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1161960769","clinical_significance":[],"start":140508406,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140508406,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795601233","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508406,"feature_type":"variation","strand":1,"alleles":["ACCCCAGCAC","AC"],"end":140508415},{"start":140508408,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140508408,"strand":1,"feature_type":"variation","id":"rs1795601255","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs545284013","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508411,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140508411},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508412,"source":"dbSNP","strand":1,"feature_type":"variation","end":140508412,"alleles":["G","C"],"seq_region_name":"7","id":"rs1795601292","clinical_significance":[]},{"seq_region_name":"7","id":"rs901784054","clinical_significance":[],"start":140508413,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140508413,"strand":1,"feature_type":"variation"},{"start":140508414,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140508414,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs997461833","clinical_significance":[]},{"end":140508415,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140508415,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs546496892"},{"seq_region_name":"7","id":"rs1367348600","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508419,"source":"dbSNP","strand":1,"feature_type":"variation","end":140508419,"alleles":["G","T"]},{"feature_type":"variation","strand":1,"end":140508420,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508420,"clinical_significance":[],"seq_region_name":"7","id":"rs1585525837"},{"seq_region_name":"7","id":"rs1182224440","clinical_significance":[],"start":140508430,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140508430,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"id":"rs954080239","seq_region_name":"7","clinical_significance":[],"end":140508431,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140508431,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795601477","source":"dbSNP","start":140508432,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140508432,"feature_type":"variation","strand":1},{"id":"rs1007264676","seq_region_name":"7","clinical_significance":[],"end":140508433,"alleles":["G","C","T"],"strand":1,"feature_type":"variation","start":140508433,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140508435,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508435,"source":"dbSNP","seq_region_name":"7","id":"rs1585525846","clinical_significance":[]},{"alleles":["A","G"],"end":140508436,"feature_type":"variation","strand":1,"source":"dbSNP","start":140508436,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795601564","seq_region_name":"7"},{"alleles":["T","C"],"end":140508439,"strand":1,"feature_type":"variation","start":140508439,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1022426419","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1250852623","source":"dbSNP","start":140508442,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140508442,"feature_type":"variation","strand":1},{"end":140508444,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140508444,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1490451347"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1467346021","source":"dbSNP","start":140508447,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140508447,"alleles":["G","A"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508450,"feature_type":"variation","strand":1,"end":140508450,"alleles":["C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1207953904"},{"end":140508456,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140508456,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795601938"},{"source":"dbSNP","start":140508467,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140508467,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs968115854"},{"seq_region_name":"7","id":"rs978284020","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140508468,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508468,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795601979","source":"dbSNP","start":140508475,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140508475,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585525853","source":"dbSNP","start":140508476,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140508476,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1280232179","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140508478,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508478,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508479,"source":"dbSNP","strand":1,"feature_type":"variation","end":140508479,"alleles":["G","A"],"seq_region_name":"7","id":"rs1795602039","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563108449","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508480,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140508480},{"clinical_significance":[],"seq_region_name":"7","id":"rs1251412116","feature_type":"variation","strand":1,"end":140508482,"alleles":["A","C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508482},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795602117","end":140508485,"alleles":["AAAA","AAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140508482,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140508486,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140508486,"alleles":["C","A","G"],"strand":1,"feature_type":"variation","id":"rs924587392","seq_region_name":"7","clinical_significance":[]},{"id":"rs1405993721","seq_region_name":"7","clinical_significance":[],"end":140508487,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140508487,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795602184","clinical_significance":[],"alleles":["C","G"],"end":140508488,"strand":1,"feature_type":"variation","start":140508488,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795602200","clinical_significance":[],"start":140508490,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140508490,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140508491,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508491,"source":"dbSNP","id":"rs1322193469","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1406241715","seq_region_name":"7","source":"dbSNP","start":140508491,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","-"],"end":140508491,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508496,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140508496,"clinical_significance":[],"id":"rs1156932975","seq_region_name":"7"},{"end":140508497,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140508497,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1411916986"},{"seq_region_name":"7","id":"rs1795602310","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508499,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AAAAA","AAAAAA"],"end":140508503},{"alleles":["T","C"],"end":140508504,"strand":1,"feature_type":"variation","start":140508504,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795602333","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1031156245","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508506,"feature_type":"variation","strand":1,"end":140508506,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1032015670","clinical_significance":[],"start":140508507,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AAAAAAA","AAAAAA","AAAAAAAA"],"end":140508513,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs955945979","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140508513,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508513},{"id":"rs1409396041","seq_region_name":"7","clinical_significance":[],"end":140508517,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140508517,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795602448","clinical_significance":[],"start":140508521,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140508527,"alleles":["GGCATAG","G"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140508527,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508527,"clinical_significance":[],"seq_region_name":"7","id":"rs1795602462"},{"feature_type":"variation","strand":1,"end":140508530,"alleles":["T","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508530,"clinical_significance":[],"seq_region_name":"7","id":"rs1795602475"},{"seq_region_name":"7","id":"rs992830128","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508532,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140508532},{"alleles":["-","GG"],"end":140508532,"feature_type":"variation","strand":1,"source":"dbSNP","start":140508533,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795602517","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795602537","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140508533,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508533,"source":"dbSNP"},{"seq_region_name":"7","id":"rs770415180","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508534,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140508534},{"strand":1,"feature_type":"variation","end":140508535,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508535,"source":"dbSNP","id":"rs1024253151","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","T"],"end":140508537,"feature_type":"variation","strand":1,"source":"dbSNP","start":140508537,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs970146494","seq_region_name":"7"},{"source":"dbSNP","start":140508538,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140508538,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs148195731"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130427580","end":140508542,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140508542,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140508544,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508544,"source":"dbSNP","seq_region_name":"7","id":"rs55928081","clinical_significance":[]},{"end":140508546,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140508546,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs992434009","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130427588","clinical_significance":[],"start":140508552,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140508552,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585525891","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508554,"feature_type":"variation","strand":1,"end":140508556,"alleles":["CAG","CAGCAG"]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140508555,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508555,"clinical_significance":[],"id":"rs530663443","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508557,"source":"dbSNP","strand":1,"feature_type":"variation","end":140508557,"alleles":["G","A"],"seq_region_name":"7","id":"rs920659519","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508561,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140508561,"clinical_significance":[],"seq_region_name":"7","id":"rs1585525896"},{"seq_region_name":"7","id":"rs1284785805","clinical_significance":[],"strand":1,"feature_type":"variation","end":140508563,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508563,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1392701684","end":140508566,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140508566,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795602808","clinical_significance":[],"strand":1,"feature_type":"variation","end":140508567,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508567,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140508570,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508570,"clinical_significance":[],"seq_region_name":"7","id":"rs1435394488"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795602847","source":"dbSNP","start":140508571,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140508571,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1298378868","clinical_significance":[],"start":140508574,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140508574,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs916782289","source":"dbSNP","start":140508575,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140508575,"alleles":["T","C","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1327143184","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508582,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140508582},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140508585,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508585,"source":"dbSNP","seq_region_name":"7","id":"rs371691650","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585525916","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508586,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140508586},{"clinical_significance":[],"seq_region_name":"7","id":"rs187145367","end":140508590,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140508590,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140508591,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140508591,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs983597475","seq_region_name":"7"},{"start":140508593,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140508593,"alleles":["A","G"],"strand":1,"feature_type":"variation","id":"rs2130427640","seq_region_name":"7","clinical_significance":[]},{"end":140508596,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140508596,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795603063","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508598,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140508598,"clinical_significance":[],"id":"rs1795603084","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508599,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140508599,"clinical_significance":[],"seq_region_name":"7","id":"rs1795603118"},{"clinical_significance":[],"id":"rs908159428","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508600,"feature_type":"variation","strand":1,"end":140508600,"alleles":["G","T"]},{"alleles":["T","A","G"],"end":140508604,"strand":1,"feature_type":"variation","start":140508604,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585525923","clinical_significance":[]},{"source":"dbSNP","start":140508605,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140508605,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs944932131"},{"end":140508606,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140508606,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1327538604","clinical_significance":[]},{"start":140508607,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140508607,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1323135128","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs984414448","source":"dbSNP","start":140508609,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140508609,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508610,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140508610,"clinical_significance":[],"seq_region_name":"7","id":"rs1157719032"},{"alleles":["C","G","T"],"end":140508615,"feature_type":"variation","strand":1,"source":"dbSNP","start":140508615,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs112116196"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140508616,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508616,"clinical_significance":[],"seq_region_name":"7","id":"rs940428107"},{"clinical_significance":[],"seq_region_name":"7","id":"rs546698021","feature_type":"variation","strand":1,"end":140508617,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508617},{"alleles":["G","A","C"],"end":140508618,"feature_type":"variation","strand":1,"source":"dbSNP","start":140508618,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1333875105"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508622,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140508622,"seq_region_name":"7","id":"rs1463630043","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1036046662","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508623,"feature_type":"variation","strand":1,"end":140508623,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795605942","feature_type":"variation","strand":1,"alleles":["TGCACTCCAGCCTGGGCAACAGTGTGAGACTCCGTCTCAAAAAAAAAAAAAAAAAAAAAGGGAAAAGGAAAATACATAACCATGGTGGTGTGTGCTTGTAACTACTTGGGAGGCTGAAGTGGGGTTGGGCCCAGGAGGTCCAAGCTGCAGTGAGCTGTGATGGTGCCATTGCACTCCAGCCTGGGCAACAG","TGCACTCCAGCCTGGGCAACAG"],"end":140508813,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508623},{"seq_region_name":"7","id":"rs1795605958","clinical_significance":[],"strand":1,"feature_type":"variation","end":140508626,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508626,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508629,"source":"dbSNP","strand":1,"feature_type":"variation","end":140508629,"alleles":["C","A"],"id":"rs1204887721","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508631,"source":"dbSNP","strand":1,"feature_type":"variation","end":140508631,"alleles":["A","G"],"id":"rs1795606001","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508638,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140508638,"clinical_significance":[],"seq_region_name":"7","id":"rs901690297"},{"strand":1,"feature_type":"variation","end":140508640,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508640,"source":"dbSNP","seq_region_name":"7","id":"rs1481719767","clinical_significance":[]},{"start":140508642,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140508642,"strand":1,"feature_type":"variation","id":"rs1314182537","seq_region_name":"7","clinical_significance":[]},{"start":140508643,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140508643,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1175579908","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508644,"feature_type":"variation","strand":1,"end":140508644,"alleles":["G","T"],"clinical_significance":[],"id":"rs1251141583","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["GTGTG","GTG"],"end":140508648,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508644,"source":"dbSNP","seq_region_name":"7","id":"rs2130427693","clinical_significance":[]},{"source":"dbSNP","start":140508645,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140508645,"alleles":["T","A","C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1475844305"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508647,"feature_type":"variation","strand":1,"end":140508647,"alleles":["T","A","C"],"clinical_significance":[],"id":"rs1219076842","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1340481709","seq_region_name":"7","alleles":["G","A"],"end":140508648,"feature_type":"variation","strand":1,"source":"dbSNP","start":140508648,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1190688432","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140508651,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508651,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1416218236","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508652,"feature_type":"variation","strand":1,"end":140508652,"alleles":["C","G"]},{"start":140508653,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C","G"],"end":140508653,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1405154256","clinical_significance":[]},{"start":140508655,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","G","T"],"end":140508655,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs57020212","clinical_significance":[]},{"seq_region_name":"7","id":"rs932283507","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140508656,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508656,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508657,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140508657,"seq_region_name":"7","id":"rs2130427712","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130427717","source":"dbSNP","start":140508658,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140508658,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140508658,"alleles":["-","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508659,"source":"dbSNP","id":"rs1795606445","seq_region_name":"7","clinical_significance":[]},{"end":140508659,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140508659,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1450183077"},{"alleles":["T","-"],"end":140508659,"feature_type":"variation","strand":1,"source":"dbSNP","start":140508659,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795606499"},{"seq_region_name":"7","id":"rs1795606523","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508660,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["-","A","AA"],"end":140508659},{"start":140508660,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140508660,"alleles":["C","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1222184692","clinical_significance":[]},{"seq_region_name":"7","id":"rs1319317017","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","-"],"end":140508660,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508660,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140508661,"alleles":["A","C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508661,"clinical_significance":[],"seq_region_name":"7","id":"rs933115680"},{"clinical_significance":[],"seq_region_name":"7","id":"rs60829150","feature_type":"variation","strand":1,"end":140508681,"alleles":["AAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAA","AAAAAAAAAAAA","AAAAAAAAAAAAA","AAAAAAAAAAAAAA","AAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508661},{"feature_type":"variation","strand":1,"end":140508670,"alleles":["-","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508671,"clinical_significance":[],"seq_region_name":"7","id":"rs1795606908"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795606933","feature_type":"variation","strand":1,"end":140508671,"alleles":["A","ACA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508671},{"source":"dbSNP","start":140508672,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140508671,"alleles":["-","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1049519617"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585525998","alleles":["A","ATA"],"end":140508672,"feature_type":"variation","strand":1,"source":"dbSNP","start":140508672,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795607003","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508675,"source":"dbSNP","strand":1,"feature_type":"variation","end":140508675,"alleles":["A","G"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508676,"feature_type":"variation","strand":1,"end":140508676,"alleles":["A","AGA","ATA"],"clinical_significance":[],"id":"rs1795607027","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["-","T"],"end":140508676,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508677,"source":"dbSNP","seq_region_name":"7","id":"rs1355502918","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795607081","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140508679,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508679,"source":"dbSNP"},{"end":140508680,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140508680,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1585526008","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508681,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["-","G"],"end":140508680,"seq_region_name":"7","id":"rs1795607132","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1342079226","alleles":["A","G","T"],"end":140508681,"feature_type":"variation","strand":1,"source":"dbSNP","start":140508681,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1585526020","clinical_significance":[],"strand":1,"feature_type":"variation","end":140508682,"alleles":["AG","AGAG"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508681,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795607224","source":"dbSNP","start":140508682,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["-","AG"],"end":140508681,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs904238834","seq_region_name":"7","alleles":["G","A","T"],"end":140508682,"feature_type":"variation","strand":1,"source":"dbSNP","start":140508682,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1291381822","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508682,"source":"dbSNP","strand":1,"feature_type":"variation","end":140508684,"alleles":["GGG","-"]},{"feature_type":"variation","strand":1,"end":140508684,"alleles":["GGG","GG"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508682,"clinical_significance":[],"seq_region_name":"7","id":"rs1795607285"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508683,"feature_type":"variation","strand":1,"end":140508683,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130427791"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1380675421","source":"dbSNP","start":140508684,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140508684,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1446872305","clinical_significance":[],"end":140508685,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140508685,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140508689,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508689,"source":"dbSNP","seq_region_name":"7","id":"rs1795607426","clinical_significance":[]},{"start":140508689,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140508690,"alleles":["GG","-"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795607466","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508690,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140508690,"seq_region_name":"7","id":"rs1795607487","clinical_significance":[]},{"alleles":["T","A","C"],"end":140508695,"strand":1,"feature_type":"variation","start":140508695,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs993311049","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1309637877","alleles":["A","C"],"end":140508696,"feature_type":"variation","strand":1,"source":"dbSNP","start":140508696,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795607552","clinical_significance":[],"start":140508697,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140508697,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140508698,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508698,"clinical_significance":[],"id":"rs1427509040","seq_region_name":"7"},{"start":140508699,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140508699,"alleles":["T","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1369945972","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508701,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140508701,"id":"rs192788148","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795607638","source":"dbSNP","start":140508702,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140508702,"feature_type":"variation","strand":1},{"alleles":["C","A","G","T"],"end":140508703,"strand":1,"feature_type":"variation","start":140508703,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs4725720","seq_region_name":"7","clinical_significance":[]},{"id":"rs1795607739","seq_region_name":"7","clinical_significance":[],"alleles":["T","A"],"end":140508705,"strand":1,"feature_type":"variation","start":140508705,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140508708,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140508708,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1585526046","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140508710,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508710,"source":"dbSNP","seq_region_name":"7","id":"rs1309537569","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1254163581","feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140508711,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508711},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508712,"feature_type":"variation","strand":1,"end":140508712,"alleles":["G","A"],"clinical_significance":[],"id":"rs1795607849","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1203249549","seq_region_name":"7","source":"dbSNP","start":140508714,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140508714,"alleles":["G","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs867411165","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140508715,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508715},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795607907","feature_type":"variation","strand":1,"end":140508717,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508717},{"seq_region_name":"7","id":"rs1050368473","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140508720,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508720,"source":"dbSNP"},{"source":"dbSNP","start":140508724,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140508724,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs73490364"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508725,"feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140508725,"clinical_significance":[],"seq_region_name":"7","id":"rs1795608045"},{"alleles":["C","G"],"end":140508727,"strand":1,"feature_type":"variation","start":140508727,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795608090","clinical_significance":[]},{"alleles":["T","G"],"end":140508729,"strand":1,"feature_type":"variation","start":140508729,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130427867","clinical_significance":[]},{"end":140508730,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140508730,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1014114074"},{"clinical_significance":[],"seq_region_name":"7","id":"rs529920469","source":"dbSNP","start":140508734,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140508734,"feature_type":"variation","strand":1},{"id":"rs1795608200","seq_region_name":"7","clinical_significance":[],"end":140508736,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140508736,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508737,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140508737,"clinical_significance":[],"id":"rs1022292503","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508740,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140508740,"clinical_significance":[],"seq_region_name":"7","id":"rs2130427882"},{"strand":1,"feature_type":"variation","end":140508741,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508741,"source":"dbSNP","seq_region_name":"7","id":"rs1472733805","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795608301","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508742,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140508742},{"clinical_significance":[],"seq_region_name":"7","id":"rs183600892","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140508746,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508746},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795608741","end":140508747,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140508747,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140508751,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140508751,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs999627460","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508752,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140508752,"seq_region_name":"7","id":"rs1031061454","clinical_significance":[]},{"end":140508753,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140508753,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1028154151","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs544677925","alleles":["C","T"],"end":140508754,"feature_type":"variation","strand":1,"source":"dbSNP","start":140508754,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["G","A"],"end":140508756,"strand":1,"feature_type":"variation","start":140508756,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795608840","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585526091","end":140508759,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140508759,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795608875","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140508760,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508760},{"clinical_significance":[],"seq_region_name":"7","id":"rs1349631241","source":"dbSNP","start":140508766,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140508766,"alleles":["G","T"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140508769,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508769,"clinical_significance":[],"seq_region_name":"7","id":"rs1259689846"},{"seq_region_name":"7","id":"rs1795608934","clinical_significance":[],"end":140508770,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140508770,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140508772,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140508772,"alleles":["G","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1294087744","clinical_significance":[]},{"alleles":["G","A"],"end":140508776,"strand":1,"feature_type":"variation","start":140508776,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs4725721","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140508785,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508785,"clinical_significance":[],"id":"rs1795609097","seq_region_name":"7"},{"end":140508787,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140508787,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1348003289"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508789,"feature_type":"variation","strand":1,"end":140508789,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1164175097"},{"feature_type":"variation","strand":1,"end":140508796,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508796,"clinical_significance":[],"seq_region_name":"7","id":"rs1023926187"},{"source":"dbSNP","start":140508797,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140508797,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs908021495"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508801,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140508801,"seq_region_name":"7","id":"rs1375619079","clinical_significance":[]},{"seq_region_name":"7","id":"rs761141503","clinical_significance":[],"end":140508803,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140508803,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["G","A","T"],"end":140508807,"strand":1,"feature_type":"variation","start":140508807,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1180260808","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508808,"feature_type":"variation","strand":1,"end":140508808,"alleles":["C","-"],"clinical_significance":[],"seq_region_name":"7","id":"rs1472491287"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508810,"source":"dbSNP","strand":1,"feature_type":"variation","end":140508810,"alleles":["A","G"],"seq_region_name":"7","id":"rs966305606","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795609648","seq_region_name":"7","end":140508811,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140508811,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508814,"feature_type":"variation","strand":1,"end":140508814,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795609678"},{"start":140508816,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140508816,"alleles":["C","A","G"],"strand":1,"feature_type":"variation","id":"rs1436050064","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","A","G","T"],"end":140508822,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508822,"source":"dbSNP","seq_region_name":"7","id":"rs4725722","clinical_significance":[]},{"clinical_significance":[],"id":"rs970033426","seq_region_name":"7","source":"dbSNP","start":140508824,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A","C"],"end":140508824,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1795609910","seq_region_name":"7","source":"dbSNP","start":140508826,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140508826,"feature_type":"variation","strand":1},{"end":140508829,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140508829,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs932313169"},{"id":"rs1795609964","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508830,"source":"dbSNP","strand":1,"feature_type":"variation","end":140508831,"alleles":["AA","AAA"]},{"clinical_significance":[],"id":"rs1585526127","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508831,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140508831},{"feature_type":"variation","strand":1,"end":140508833,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508833,"clinical_significance":[],"id":"rs1329222249","seq_region_name":"7"},{"start":140508834,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140508834,"alleles":["A","G","T"],"strand":1,"feature_type":"variation","id":"rs984447269","seq_region_name":"7","clinical_significance":[]},{"end":140508844,"alleles":["AAAAAAAAAAA","AAAAAAAAAA","AAAAAAAAAAAA","AAAAAAAAAAAAA"],"strand":1,"feature_type":"variation","start":140508834,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs61008035","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130427990","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508835,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["-","T"],"end":140508834},{"id":"rs1049365270","seq_region_name":"7","clinical_significance":[],"end":140508836,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140508836,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140508838,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140508838,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs908903805","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795610249","seq_region_name":"7","end":140508844,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140508844,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140508847,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140508847,"strand":1,"feature_type":"variation","id":"rs1301748506","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508849,"feature_type":"variation","strand":1,"end":140508849,"alleles":["C","T"],"clinical_significance":[],"id":"rs1795610299","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795610331","feature_type":"variation","strand":1,"end":140508850,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508850},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508852,"source":"dbSNP","strand":1,"feature_type":"variation","end":140508852,"alleles":["A","G"],"seq_region_name":"7","id":"rs1388226218","clinical_significance":[]},{"clinical_significance":[],"id":"rs1271756423","seq_region_name":"7","alleles":["T","A"],"end":140508853,"feature_type":"variation","strand":1,"source":"dbSNP","start":140508853,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508855,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140508855,"clinical_significance":[],"id":"rs2130428010","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs138022717","feature_type":"variation","strand":1,"end":140508858,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508858},{"clinical_significance":[],"seq_region_name":"7","id":"rs754007231","source":"dbSNP","start":140508862,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140508862,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1325118663","clinical_significance":[],"start":140508867,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140508867,"alleles":["T","A","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1435963780","clinical_significance":[],"start":140508869,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140508869,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508872,"source":"dbSNP","strand":1,"feature_type":"variation","end":140508872,"alleles":["G","A"],"id":"rs1795610531","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","C"],"end":140508883,"feature_type":"variation","strand":1,"source":"dbSNP","start":140508883,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795610557"},{"seq_region_name":"7","id":"rs553015980","clinical_significance":[],"start":140508884,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140508884,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1795610597","clinical_significance":[],"strand":1,"feature_type":"variation","end":140508889,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508889,"source":"dbSNP"},{"alleles":["G","A"],"end":140508892,"strand":1,"feature_type":"variation","start":140508892,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs115645333","clinical_significance":[]},{"source":"dbSNP","start":140508896,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140508896,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1053392378"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140508899,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508899,"clinical_significance":[],"id":"rs1795610694","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1456934730","seq_region_name":"7","feature_type":"variation","strand":1,"end":140508902,"alleles":["T","TT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508902},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140508903,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508903,"source":"dbSNP","seq_region_name":"7","id":"rs971795844","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795610775","feature_type":"variation","strand":1,"end":140508903,"alleles":["A","AA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508903},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508904,"feature_type":"variation","strand":1,"end":140508904,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795610798"},{"feature_type":"variation","strand":1,"end":140508905,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508905,"clinical_significance":[],"id":"rs73490368","seq_region_name":"7"},{"id":"rs1795610869","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140508907,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508907,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508908,"source":"dbSNP","strand":1,"feature_type":"variation","end":140508908,"alleles":["T","G"],"seq_region_name":"7","id":"rs1795610900","clinical_significance":[]},{"start":140508913,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140508913,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795610932","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140508914,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508914,"clinical_significance":[],"id":"rs1795610958","seq_region_name":"7"},{"end":140508920,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140508920,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1585526160","seq_region_name":"7"},{"alleles":["A","G"],"end":140508923,"strand":1,"feature_type":"variation","start":140508923,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795611020","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140508924,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508924,"source":"dbSNP","seq_region_name":"7","id":"rs557333015","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795611076","seq_region_name":"7","end":140508927,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140508927,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795611102","feature_type":"variation","strand":1,"end":140508930,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508930},{"clinical_significance":[],"seq_region_name":"7","id":"rs369005193","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508934,"feature_type":"variation","strand":1,"alleles":["T","A","G"],"end":140508934},{"seq_region_name":"7","id":"rs1050676904","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508940,"source":"dbSNP","strand":1,"feature_type":"variation","end":140508940,"alleles":["G","A"]},{"source":"dbSNP","start":140508946,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140508946,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130428074"},{"clinical_significance":[],"seq_region_name":"7","id":"rs575480814","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508949,"feature_type":"variation","strand":1,"end":140508949,"alleles":["C","A","T"]},{"clinical_significance":[],"id":"rs1249385315","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508950,"feature_type":"variation","strand":1,"end":140508950,"alleles":["C","G"]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140508953,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508953,"source":"dbSNP","seq_region_name":"7","id":"rs1585526175","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795611283","clinical_significance":[],"start":140508957,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140508957,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140508959,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508959,"source":"dbSNP","seq_region_name":"7","id":"rs1795611310","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1001527998","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140508960,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508960},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508967,"feature_type":"variation","strand":1,"end":140508967,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795611368"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130428090","feature_type":"variation","strand":1,"end":140508969,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508969},{"id":"rs1349524717","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140508972,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508972,"source":"dbSNP"},{"seq_region_name":"7","id":"rs947268412","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140508975,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140508975},{"clinical_significance":[],"seq_region_name":"7","id":"rs1485107123","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508988,"feature_type":"variation","strand":1,"end":140508988,"alleles":["A","G"]},{"clinical_significance":[],"id":"rs1795611488","seq_region_name":"7","end":140508989,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140508989,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1829770","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140508990,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508990},{"feature_type":"variation","strand":1,"end":140508992,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508992,"clinical_significance":[],"id":"rs1795611673","seq_region_name":"7"},{"alleles":["T","C"],"end":140508993,"feature_type":"variation","strand":1,"source":"dbSNP","start":140508993,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1302631373"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140508997,"feature_type":"variation","strand":1,"end":140508997,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795611728"},{"source":"dbSNP","start":140508999,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140508999,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795611751"},{"source":"dbSNP","start":140509000,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140509000,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs188491468"},{"id":"rs1585526206","seq_region_name":"7","clinical_significance":[],"end":140509001,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140509001,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140509002,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509002,"clinical_significance":[],"seq_region_name":"7","id":"rs1795611841"},{"strand":1,"feature_type":"variation","end":140509003,"alleles":["CC","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509002,"source":"dbSNP","id":"rs1795611872","seq_region_name":"7","clinical_significance":[]},{"end":140509005,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140509005,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1367208381","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","G"],"end":140509006,"feature_type":"variation","strand":1,"source":"dbSNP","start":140509006,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs999490201","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509007,"feature_type":"variation","strand":1,"end":140509007,"alleles":["C","A"],"clinical_significance":[],"id":"rs1795611946","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1585526215","clinical_significance":[],"start":140509009,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140509009,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509012,"source":"dbSNP","strand":1,"feature_type":"variation","end":140509012,"alleles":["T","C"],"seq_region_name":"7","id":"rs1031085372","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795612037","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509014,"source":"dbSNP","strand":1,"feature_type":"variation","end":140509014,"alleles":["T","A"]},{"start":140509015,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140509015,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795612067","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130428143","clinical_significance":[],"strand":1,"feature_type":"variation","end":140509016,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509016,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1381653802","source":"dbSNP","start":140509021,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140509021,"alleles":["A","G"],"feature_type":"variation","strand":1},{"id":"rs1318634379","seq_region_name":"7","clinical_significance":[],"alleles":["AAAAAAA","AAAAAA","AAAAAAAA"],"end":140509027,"strand":1,"feature_type":"variation","start":140509021,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509023,"source":"dbSNP","strand":1,"feature_type":"variation","end":140509023,"alleles":["A","G","T"],"seq_region_name":"7","id":"rs1795612163","clinical_significance":[]},{"id":"rs1795612199","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140509024,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509024,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509028,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140509028,"clinical_significance":[],"id":"rs528591316","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795612272","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509037,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140509037},{"source":"dbSNP","start":140509038,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140509038,"alleles":["A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795612303","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140509039,"alleles":["AG","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509038,"clinical_significance":[],"id":"rs1423818783","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1795612350","seq_region_name":"7","alleles":["G","A"],"end":140509039,"feature_type":"variation","strand":1,"source":"dbSNP","start":140509039,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509041,"source":"dbSNP","strand":1,"feature_type":"variation","end":140509041,"alleles":["G","A"],"seq_region_name":"7","id":"rs540288028","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795612408","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140509042,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509042,"source":"dbSNP"},{"clinical_significance":[],"id":"rs2130428168","seq_region_name":"7","feature_type":"variation","strand":1,"end":140509044,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509044},{"seq_region_name":"7","id":"rs1320193249","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140509047,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509047,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509048,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140509048,"id":"rs1795612461","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140509049,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509049,"source":"dbSNP","seq_region_name":"7","id":"rs1795612486","clinical_significance":[]},{"seq_region_name":"7","id":"rs1024206943","clinical_significance":[],"strand":1,"feature_type":"variation","end":140509055,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509055,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795612534","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509057,"feature_type":"variation","strand":1,"end":140509057,"alleles":["A","G"]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140509058,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509058,"source":"dbSNP","seq_region_name":"7","id":"rs1795612552","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140509061,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509061,"source":"dbSNP","seq_region_name":"7","id":"rs2130428188","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509063,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140509063,"seq_region_name":"7","id":"rs1394830899","clinical_significance":[]},{"id":"rs371625969","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140509065,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509065,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1451908058","end":140509068,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140509068,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1388798535","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509069,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140509069},{"clinical_significance":[],"id":"rs1795614676","seq_region_name":"7","end":140509084,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140509084,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509085,"feature_type":"variation","strand":1,"end":140509085,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1434095253"},{"alleles":["C","T"],"end":140509089,"feature_type":"variation","strand":1,"source":"dbSNP","start":140509089,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795614719"},{"seq_region_name":"7","id":"rs1186194873","clinical_significance":[],"alleles":["T","-"],"end":140509090,"strand":1,"feature_type":"variation","start":140509090,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795614760","clinical_significance":[],"alleles":["G","T"],"end":140509093,"strand":1,"feature_type":"variation","start":140509093,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509094,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140509094,"clinical_significance":[],"seq_region_name":"7","id":"rs1326288050"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1372026878","source":"dbSNP","start":140509095,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140509095,"alleles":["C","T"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509096,"feature_type":"variation","strand":1,"end":140509096,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1201781816"},{"seq_region_name":"7","id":"rs1795614835","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509102,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140509102},{"seq_region_name":"7","id":"rs1482048324","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509105,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140509105},{"start":140509107,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140509107,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1279370998","clinical_significance":[]},{"id":"rs1795614899","seq_region_name":"7","clinical_significance":[],"start":140509108,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140509108,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509109,"feature_type":"variation","strand":1,"end":140509109,"alleles":["G","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795614920"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509112,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140509112,"clinical_significance":[],"seq_region_name":"7","id":"rs1795614935"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140509114,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509114,"clinical_significance":[],"seq_region_name":"7","id":"rs1795614949"},{"clinical_significance":[],"seq_region_name":"7","id":"rs532415549","feature_type":"variation","strand":1,"end":140509119,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509119},{"id":"rs1795614986","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509122,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140509122},{"end":140509123,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140509123,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795614998","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140509125,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509125,"source":"dbSNP","id":"rs193169540","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795615051","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509126,"source":"dbSNP","strand":1,"feature_type":"variation","end":140509126,"alleles":["A","-"]},{"seq_region_name":"7","id":"rs147198619","clinical_significance":[],"start":140509128,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140509128,"alleles":["C","G","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1295310954","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509130,"source":"dbSNP","strand":1,"feature_type":"variation","end":140509130,"alleles":["G","A"]},{"feature_type":"variation","strand":1,"end":140509132,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509132,"clinical_significance":[],"seq_region_name":"7","id":"rs2130428244"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795615133","feature_type":"variation","strand":1,"end":140509133,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509133},{"seq_region_name":"7","id":"rs1016436755","clinical_significance":[],"start":140509134,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140509134,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509135,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140509135,"seq_region_name":"7","id":"rs1795615178","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795615195","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509136,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140509136},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509137,"feature_type":"variation","strand":1,"end":140509137,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795615216"},{"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140509139,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509139,"clinical_significance":[],"seq_region_name":"7","id":"rs1795615233"},{"source":"dbSNP","start":140509140,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140509140,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795615250","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140509141,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509141,"clinical_significance":[],"id":"rs530394370","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795615326","clinical_significance":[],"alleles":["T","C"],"end":140509142,"strand":1,"feature_type":"variation","start":140509142,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140509143,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140509143,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1341118420"},{"alleles":["C","T"],"end":140509150,"feature_type":"variation","strand":1,"source":"dbSNP","start":140509150,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795615378"},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140509152,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509152,"source":"dbSNP","seq_region_name":"7","id":"rs1315156360","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509153,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140509153,"id":"rs10952706","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","C","G"],"end":140509154,"strand":1,"feature_type":"variation","start":140509154,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs985566141","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140509158,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509158,"clinical_significance":[],"seq_region_name":"7","id":"rs1795615621"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509161,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140509161,"clinical_significance":[],"seq_region_name":"7","id":"rs1795615663"},{"alleles":["A","C"],"end":140509164,"strand":1,"feature_type":"variation","start":140509164,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs971704091","clinical_significance":[]},{"end":140509174,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140509174,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795615743"},{"id":"rs923077810","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140509177,"strand":1,"feature_type":"variation","start":140509177,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795615796","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140509180,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509180},{"source":"dbSNP","start":140509183,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140509183,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795615828"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509185,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140509185,"clinical_significance":[],"seq_region_name":"7","id":"rs1369306002"},{"strand":1,"feature_type":"variation","end":140509186,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509186,"source":"dbSNP","id":"rs796809806","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140509187,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A","C"],"end":140509187,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795615970"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795616003","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140509188,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509188},{"clinical_significance":[],"seq_region_name":"7","id":"rs986004959","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509189,"feature_type":"variation","strand":1,"end":140509189,"alleles":["G","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509190,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140509190,"clinical_significance":[],"seq_region_name":"7","id":"rs910395502"},{"end":140509193,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140509193,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795616085"},{"end":140509197,"alleles":["CCCCC","CCCC"],"strand":1,"feature_type":"variation","start":140509193,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795616111","seq_region_name":"7","clinical_significance":[]},{"start":140509194,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140509194,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795616132","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1188962708","feature_type":"variation","strand":1,"end":140509195,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509195},{"alleles":["C","G"],"end":140509196,"feature_type":"variation","strand":1,"source":"dbSNP","start":140509196,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795616172"},{"clinical_significance":[],"id":"rs1421700340","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509197,"feature_type":"variation","strand":1,"end":140509197,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1256285187","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140509199,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509199,"source":"dbSNP"},{"seq_region_name":"7","id":"rs947172195","clinical_significance":[],"alleles":["C","T"],"end":140509200,"strand":1,"feature_type":"variation","start":140509200,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140509205,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G","T"],"end":140509205,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs567015428","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795616358","clinical_significance":[],"start":140509209,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140509209,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"end":140509213,"alleles":["T","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140509213,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795616388","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1470212737","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509214,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140509214},{"clinical_significance":[],"seq_region_name":"7","id":"rs1159727685","source":"dbSNP","start":140509218,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140509218,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1052885382","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509223,"source":"dbSNP","strand":1,"feature_type":"variation","end":140509223,"alleles":["G","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509224,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140509224,"clinical_significance":[],"seq_region_name":"7","id":"rs1795616516"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140509233,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509233,"source":"dbSNP","id":"rs1795616548","seq_region_name":"7","clinical_significance":[]},{"start":140509235,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140509235,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1405741511","clinical_significance":[]},{"id":"rs1795616605","seq_region_name":"7","clinical_significance":[],"start":140509237,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140509237,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"alleles":["A","G"],"end":140509240,"strand":1,"feature_type":"variation","start":140509240,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1165436560","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509242,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140509242,"clinical_significance":[],"seq_region_name":"7","id":"rs1396365556"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1267330872","source":"dbSNP","start":140509247,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140509247,"alleles":["C","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795616721","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140509250,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509250,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795616747","end":140509255,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140509255,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1585526290","clinical_significance":[],"start":140509256,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140509256,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1242628140","clinical_significance":[],"start":140509257,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C"],"end":140509257,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795616834","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509260,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140509260},{"seq_region_name":"7","id":"rs1355069416","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509261,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C","T"],"end":140509261},{"seq_region_name":"7","id":"rs1289201151","clinical_significance":[],"alleles":["T","C"],"end":140509263,"strand":1,"feature_type":"variation","start":140509263,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795616924","alleles":["G","A"],"end":140509264,"feature_type":"variation","strand":1,"source":"dbSNP","start":140509264,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140509265,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140509265,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1563108672","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795616966","feature_type":"variation","strand":1,"end":140509269,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509269},{"seq_region_name":"7","id":"rs142904757","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509270,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140509270},{"end":140509271,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140509271,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1348978678","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795617022","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140509274,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509274,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1795617051","seq_region_name":"7","end":140509276,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140509276,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140509277,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140509277,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795617069","clinical_significance":[]},{"end":140509278,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140509278,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs924481947"},{"seq_region_name":"7","id":"rs1795617105","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509279,"source":"dbSNP","strand":1,"feature_type":"variation","end":140509279,"alleles":["T","C","G"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509280,"feature_type":"variation","strand":1,"end":140509280,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1330677888"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140509281,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509281,"source":"dbSNP","seq_region_name":"7","id":"rs1795617152","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509282,"feature_type":"variation","strand":1,"end":140509282,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1443065851"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795617173","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509283,"feature_type":"variation","strand":1,"end":140509283,"alleles":["G","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1281309634","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140509286,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509286},{"seq_region_name":"7","id":"rs754873093","clinical_significance":[],"alleles":["T","A"],"end":140509292,"strand":1,"feature_type":"variation","start":140509292,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795617229","clinical_significance":[],"alleles":["C","T"],"end":140509294,"strand":1,"feature_type":"variation","start":140509294,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["A","C"],"end":140509295,"strand":1,"feature_type":"variation","start":140509295,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795617244","clinical_significance":[]},{"source":"dbSNP","start":140509296,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140509296,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs575093438"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1164497942","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509300,"feature_type":"variation","strand":1,"end":140509302,"alleles":["GGG","GG"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509302,"feature_type":"variation","strand":1,"end":140509302,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795617292"},{"clinical_significance":[],"seq_region_name":"7","id":"rs896594989","source":"dbSNP","start":140509303,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140509303,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140509304,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140509304,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1014108071"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1349239509","end":140509306,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140509306,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1795617380","seq_region_name":"7","alleles":["AG","AGAG"],"end":140509308,"feature_type":"variation","strand":1,"source":"dbSNP","start":140509307,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140509308,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140509308,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1416793711","seq_region_name":"7"},{"end":140509309,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140509309,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795618367","seq_region_name":"7","clinical_significance":[]},{"start":140509314,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140509317,"alleles":["CTCT","CT"],"strand":1,"feature_type":"variation","id":"rs1228287630","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1473473750","clinical_significance":[],"end":140509316,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140509316,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795618447","clinical_significance":[],"strand":1,"feature_type":"variation","end":140509332,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509332,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509334,"source":"dbSNP","strand":1,"feature_type":"variation","end":140509334,"alleles":["A","G"],"seq_region_name":"7","id":"rs571356535","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140509336,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509336,"source":"dbSNP","id":"rs1585526318","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","G"],"end":140509344,"strand":1,"feature_type":"variation","start":140509344,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795618507","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140509352,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509352,"clinical_significance":[],"seq_region_name":"7","id":"rs1795618529"},{"seq_region_name":"7","id":"rs1795618552","clinical_significance":[],"alleles":["G","A"],"end":140509356,"strand":1,"feature_type":"variation","start":140509356,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795618580","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140509359,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509359,"source":"dbSNP"},{"end":140509361,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140509361,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795618615","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","C"],"end":140509363,"strand":1,"feature_type":"variation","start":140509363,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1180768215","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140509365,"alleles":["T","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509365,"source":"dbSNP","id":"rs1045537012","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140509371,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509371,"source":"dbSNP","seq_region_name":"7","id":"rs1795618718","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795618745","clinical_significance":[],"end":140509380,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140509380,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795618762","clinical_significance":[],"end":140509382,"alleles":["TTT","TTTT"],"strand":1,"feature_type":"variation","start":140509380,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1269296670","alleles":["TTTGTTT","TTT"],"end":140509386,"feature_type":"variation","strand":1,"source":"dbSNP","start":140509380,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["TGT","T"],"end":140509384,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509382,"clinical_significance":[],"seq_region_name":"7","id":"rs1208211571"},{"seq_region_name":"7","id":"rs1795618867","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["-","TC"],"end":140509382,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509383,"source":"dbSNP"},{"seq_region_name":"7","id":"rs10236997","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509383,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C","T"],"end":140509383},{"end":140509383,"alleles":["G","-"],"strand":1,"feature_type":"variation","start":140509383,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs879870146","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs386718476","source":"dbSNP","start":140509383,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140509384,"alleles":["GT","TC"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1554455160","clinical_significance":[],"strand":1,"feature_type":"variation","end":140509384,"alleles":["GT","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509383,"source":"dbSNP"},{"start":140509383,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140509388,"alleles":["GTTTTC","-"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs905821740","clinical_significance":[]},{"end":140509384,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","start":140509384,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs10258000","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1554455159","source":"dbSNP","start":140509384,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140509387,"alleles":["TTTT","TTT"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140509385,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140509385,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1438005044","seq_region_name":"7"},{"id":"rs1327274174","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140509386,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509386,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1183382571","source":"dbSNP","start":140509387,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["-","C","CTC"],"end":140509386,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140509401,"alleles":["TCTCTCTCTCTCTCT","TCTCTCTCTCTCT","TCTCTCTCTCTCTCTCTCT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509387,"clinical_significance":[],"id":"rs1795619936","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140509388,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509388,"clinical_significance":[],"seq_region_name":"7","id":"rs1006307128"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1248958509","source":"dbSNP","start":140509388,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140509388,"alleles":["C","-"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1472244905","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509389,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140509389},{"clinical_significance":[],"id":"rs1188557968","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140509390,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509390},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795620044","end":140509391,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140509391,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs553457736","seq_region_name":"7","clinical_significance":[],"start":140509392,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140509392,"alleles":["C","G","T"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140509396,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140509396,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1438145889"},{"seq_region_name":"7","id":"rs1005264687","clinical_significance":[],"strand":1,"feature_type":"variation","end":140509407,"alleles":["TCTTTCTTT","TCTTT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509399,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1458513719","feature_type":"variation","strand":1,"end":140509403,"alleles":["TTT","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509401},{"seq_region_name":"7","id":"rs1795620201","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509401,"source":"dbSNP","strand":1,"feature_type":"variation","end":140509409,"alleles":["TTTCTTTTT","TTT"]},{"end":140509402,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140509402,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1459688761"},{"feature_type":"variation","strand":1,"end":140509404,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509404,"clinical_significance":[],"seq_region_name":"7","id":"rs1795620254"},{"seq_region_name":"7","id":"rs1157788672","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509405,"source":"dbSNP","strand":1,"feature_type":"variation","end":140509411,"alleles":["TTTTTTT","TTTTTT"]},{"source":"dbSNP","start":140509410,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140509410,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795620314"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509411,"feature_type":"variation","strand":1,"end":140509411,"alleles":["T","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1478232629"},{"id":"rs1015017724","seq_region_name":"7","clinical_significance":[],"start":140509413,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AGAAG","AG"],"end":140509417,"strand":1,"feature_type":"variation"},{"id":"rs1016510413","seq_region_name":"7","clinical_significance":[],"start":140509414,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140509414,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"alleles":["G","A"],"end":140509417,"strand":1,"feature_type":"variation","start":140509417,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795620380","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795620398","source":"dbSNP","start":140509417,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140509438,"alleles":["GGAGTCTCGCTCTGTCACCAGG","-"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140509418,"alleles":["G","A","C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509418,"clinical_significance":[],"seq_region_name":"7","id":"rs901889816"},{"strand":1,"feature_type":"variation","end":140509421,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509421,"source":"dbSNP","seq_region_name":"7","id":"rs1467943436","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1390321778","source":"dbSNP","start":140509422,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140509422,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140509423,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140509423,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1210605509"},{"end":140509424,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140509424,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1463717275"},{"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140509425,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509425,"clinical_significance":[],"seq_region_name":"7","id":"rs144674896"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795620583","feature_type":"variation","strand":1,"end":140509426,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509426},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509432,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140509432,"id":"rs1029159153","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1366496831","clinical_significance":[],"end":140509434,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140509434,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509434,"source":"dbSNP","strand":1,"feature_type":"variation","end":140509435,"alleles":["CC","CCC"],"seq_region_name":"7","id":"rs1410727707","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1234243225","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509435,"feature_type":"variation","strand":1,"alleles":["-","T"],"end":140509434},{"seq_region_name":"7","id":"rs993204803","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509436,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140509436},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509439,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140509439,"clinical_significance":[],"seq_region_name":"7","id":"rs1030391959"},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140509442,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509442,"clinical_significance":[],"seq_region_name":"7","id":"rs1436567888"},{"source":"dbSNP","start":140509443,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140509443,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795620744"},{"seq_region_name":"7","id":"rs1348704536","clinical_significance":[],"strand":1,"feature_type":"variation","end":140509445,"alleles":["T","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509445,"source":"dbSNP"},{"seq_region_name":"7","id":"rs954379006","clinical_significance":[],"end":140509446,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140509446,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1414863629","source":"dbSNP","start":140509447,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140509447,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs184551356","clinical_significance":[],"strand":1,"feature_type":"variation","end":140509448,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509448,"source":"dbSNP"},{"id":"rs1795620856","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140509449,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509449,"source":"dbSNP"},{"end":140509452,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140509452,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795620883"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1171465064","end":140509453,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140509453,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1357843163","clinical_significance":[],"start":140509454,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140509454,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140509455,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509455,"clinical_significance":[],"seq_region_name":"7","id":"rs1795620933"},{"source":"dbSNP","start":140509456,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140509456,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs910267415"},{"clinical_significance":[],"id":"rs968540300","seq_region_name":"7","feature_type":"variation","strand":1,"end":140509461,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509461},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509462,"source":"dbSNP","strand":1,"feature_type":"variation","end":140509462,"alleles":["G","A","T"],"seq_region_name":"7","id":"rs554475914","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509465,"feature_type":"variation","strand":1,"end":140509465,"alleles":["T","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1241795250"},{"seq_region_name":"7","id":"rs1211050968","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140509471,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509471,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795621081","clinical_significance":[],"strand":1,"feature_type":"variation","end":140509472,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509472,"source":"dbSNP"},{"start":140509474,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140509474,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1444303269","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795621118","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509475,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140509475},{"seq_region_name":"7","id":"rs1278664749","clinical_significance":[],"start":140509478,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140509478,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs924555622","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509479,"feature_type":"variation","strand":1,"end":140509479,"alleles":["G","A"]},{"end":140509480,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140509480,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1343510830"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509482,"feature_type":"variation","strand":1,"end":140509482,"alleles":["T","C"],"clinical_significance":[],"id":"rs934547221","seq_region_name":"7"},{"source":"dbSNP","start":140509483,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140509483,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs949794277"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795621251","alleles":["C","A"],"end":140509484,"feature_type":"variation","strand":1,"source":"dbSNP","start":140509484,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1359211134","seq_region_name":"7","clinical_significance":[],"end":140509485,"alleles":["C","A","G","T"],"strand":1,"feature_type":"variation","start":140509485,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1585526430","clinical_significance":[],"start":140509486,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140509486,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1482433198","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140509489,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509489,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509491,"source":"dbSNP","strand":1,"feature_type":"variation","end":140509491,"alleles":["C","T"],"seq_region_name":"7","id":"rs1563108731","clinical_significance":[]},{"id":"rs1057026272","seq_region_name":"7","clinical_significance":[],"alleles":["C","A","G","T"],"end":140509493,"strand":1,"feature_type":"variation","start":140509493,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1795621384","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509494,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140509494},{"alleles":["C","G","T"],"end":140509495,"feature_type":"variation","strand":1,"source":"dbSNP","start":140509495,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs572945225"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509496,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","G"],"end":140509496,"id":"rs1433863152","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140509502,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509502,"clinical_significance":[],"seq_region_name":"7","id":"rs917927164"},{"seq_region_name":"7","id":"rs1795621463","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509510,"source":"dbSNP","strand":1,"feature_type":"variation","end":140509510,"alleles":["A","G"]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140509512,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509512,"clinical_significance":[],"seq_region_name":"7","id":"rs1371149898"},{"seq_region_name":"7","id":"rs747881757","clinical_significance":[],"end":140509516,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140509516,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140509517,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","G","T"],"end":140509517,"strand":1,"feature_type":"variation","id":"rs1045559556","seq_region_name":"7","clinical_significance":[]},{"id":"rs1421939170","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140509518,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509518,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795621609","source":"dbSNP","start":140509519,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140509519,"alleles":["A","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585526456","source":"dbSNP","start":140509520,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140509520,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1255594188","clinical_significance":[],"start":140509521,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140509521,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509524,"feature_type":"variation","strand":1,"end":140509524,"alleles":["C","T"],"clinical_significance":[],"id":"rs937146422","seq_region_name":"7"},{"start":140509525,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140509525,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1483580838","clinical_significance":[]},{"seq_region_name":"7","id":"rs376302747","clinical_significance":[],"start":140509530,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140509530,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs905284724","clinical_significance":[],"start":140509534,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140509534,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1186641180","clinical_significance":[],"strand":1,"feature_type":"variation","end":140509537,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509537,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795621808","clinical_significance":[],"start":140509538,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140509538,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"alleles":["C","T"],"end":140509541,"feature_type":"variation","strand":1,"source":"dbSNP","start":140509541,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1006380868","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs148520874","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509542,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140509542},{"end":140509544,"alleles":["GCT","ACC"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140509542,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs386718477","seq_region_name":"7"},{"clinical_significance":[],"id":"rs142860977","seq_region_name":"7","end":140509544,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140509544,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509547,"source":"dbSNP","strand":1,"feature_type":"variation","end":140509547,"alleles":["C","T"],"seq_region_name":"7","id":"rs781727562","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs940704869","source":"dbSNP","start":140509550,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140509550,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509551,"source":"dbSNP","strand":1,"feature_type":"variation","end":140509551,"alleles":["C","A"],"seq_region_name":"7","id":"rs1795621989","clinical_significance":[]},{"clinical_significance":[],"id":"rs1291040024","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509553,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140509553},{"clinical_significance":[],"seq_region_name":"7","id":"rs1413992941","source":"dbSNP","start":140509554,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140509554,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509555,"source":"dbSNP","strand":1,"feature_type":"variation","end":140509555,"alleles":["G","A"],"seq_region_name":"7","id":"rs1795622053","clinical_significance":[]},{"clinical_significance":[],"id":"rs1368886602","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509559,"feature_type":"variation","strand":1,"end":140509559,"alleles":["A","G","T"]},{"source":"dbSNP","start":140509560,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140509560,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs994173521","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509560,"source":"dbSNP","strand":1,"feature_type":"variation","end":140509565,"alleles":["TTTTTT","TTTTT"],"seq_region_name":"7","id":"rs1795622125","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140509566,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509566,"clinical_significance":[],"id":"rs1030554354","seq_region_name":"7"},{"alleles":["T","C"],"end":140509570,"strand":1,"feature_type":"variation","start":140509570,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795622207","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130428698","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509572,"source":"dbSNP","strand":1,"feature_type":"variation","end":140509572,"alleles":["T","C"]},{"id":"rs1429192403","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140509575,"strand":1,"feature_type":"variation","start":140509575,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140509576,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140509576,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795622246","clinical_significance":[]},{"start":140509580,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140509580,"alleles":["G","C"],"strand":1,"feature_type":"variation","id":"rs1795622268","seq_region_name":"7","clinical_significance":[]},{"id":"rs1795622298","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140509582,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509582,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1460427282","source":"dbSNP","start":140509583,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140509583,"alleles":["A","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1353799255","end":140509585,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140509585,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1313514103","seq_region_name":"7","clinical_significance":[],"start":140509586,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140509586,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140509588,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140509588,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1585526481","seq_region_name":"7"},{"source":"dbSNP","start":140509593,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140509593,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1377821163"},{"id":"rs890123479","seq_region_name":"7","clinical_significance":[],"start":140509594,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140509594,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509596,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140509596,"seq_region_name":"7","id":"rs1165582245","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1407152256","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509599,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140509599},{"seq_region_name":"7","id":"rs1416040545","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509600,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140509600},{"alleles":["A","G"],"end":140509604,"strand":1,"feature_type":"variation","start":140509604,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1164457045","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509606,"source":"dbSNP","strand":1,"feature_type":"variation","end":140509606,"alleles":["A","G"],"seq_region_name":"7","id":"rs1007185685","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509607,"source":"dbSNP","strand":1,"feature_type":"variation","end":140509607,"alleles":["T","C"],"seq_region_name":"7","id":"rs1333969955","clinical_significance":[]},{"seq_region_name":"7","id":"rs1036362925","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509608,"source":"dbSNP","strand":1,"feature_type":"variation","end":140509608,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1795622770","clinical_significance":[],"end":140509609,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140509609,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140509612,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509612,"clinical_significance":[],"seq_region_name":"7","id":"rs1017403075"},{"alleles":["C","G","T"],"end":140509613,"feature_type":"variation","strand":1,"source":"dbSNP","start":140509613,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1175785853","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509615,"source":"dbSNP","strand":1,"feature_type":"variation","end":140509615,"alleles":["A","G"],"seq_region_name":"7","id":"rs1795622857","clinical_significance":[]},{"alleles":["C","A"],"end":140509617,"feature_type":"variation","strand":1,"source":"dbSNP","start":140509617,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795622887"},{"clinical_significance":[],"id":"rs1795622923","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509618,"feature_type":"variation","strand":1,"end":140509618,"alleles":["T","A","C"]},{"start":140509619,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140509619,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs576909141","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585526507","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140509623,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509623},{"id":"rs1795622999","seq_region_name":"7","clinical_significance":[],"start":140509624,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140509624,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140509627,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140509627,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs901963208"},{"strand":1,"feature_type":"variation","end":140509628,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509628,"source":"dbSNP","id":"rs968447319","seq_region_name":"7","clinical_significance":[]},{"end":140509631,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140509631,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795623098","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140509634,"alleles":["CC","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509633,"clinical_significance":[],"id":"rs756042172","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509634,"feature_type":"variation","strand":1,"end":140509634,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1221734457"},{"id":"rs978616152","seq_region_name":"7","clinical_significance":[],"alleles":["G","A","C","T"],"end":140509635,"strand":1,"feature_type":"variation","start":140509635,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140509636,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140509636,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795623236"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509641,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140509641,"clinical_significance":[],"seq_region_name":"7","id":"rs544223264"},{"strand":1,"feature_type":"variation","end":140509644,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509644,"source":"dbSNP","seq_region_name":"7","id":"rs1795623285","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1031528738","feature_type":"variation","strand":1,"end":140509647,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509647},{"seq_region_name":"7","id":"rs1029190143","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140509650,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509650,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1340935997","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140509651,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509651,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509652,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140509652,"id":"rs1308899242","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","G"],"end":140509653,"strand":1,"feature_type":"variation","start":140509653,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1234415907","clinical_significance":[]},{"end":140509657,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140509657,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1389394623"},{"id":"rs955872664","seq_region_name":"7","clinical_significance":[],"end":140509660,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140509660,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1372609425","feature_type":"variation","strand":1,"end":140509661,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509661},{"id":"rs1795623552","seq_region_name":"7","clinical_significance":[],"start":140509665,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140509665,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1795623570","clinical_significance":[],"alleles":["A","G"],"end":140509666,"strand":1,"feature_type":"variation","start":140509666,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140509671,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140509671,"strand":1,"feature_type":"variation","id":"rs1281818584","seq_region_name":"7","clinical_significance":[]},{"end":140509672,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140509672,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130428787"},{"seq_region_name":"7","id":"rs1438766531","clinical_significance":[],"strand":1,"feature_type":"variation","end":140509674,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509674,"source":"dbSNP"},{"start":140509678,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140509678,"alleles":["C","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs889308106","clinical_significance":[]},{"clinical_significance":[],"id":"rs1482261027","seq_region_name":"7","end":140509681,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140509681,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140509682,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140509682,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs993164811"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140509687,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509687,"clinical_significance":[],"seq_region_name":"7","id":"rs917134916"},{"start":140509688,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140509688,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs562868730","clinical_significance":[]},{"start":140509689,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140509689,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795623828","clinical_significance":[]},{"clinical_significance":[],"id":"rs777477445","seq_region_name":"7","source":"dbSNP","start":140509690,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140509690,"alleles":["C","A","G"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509692,"feature_type":"variation","strand":1,"end":140509714,"alleles":["TTTTTATTTTTATTTTTATTTTT","TTTTTATTTTTATTTTT","TTTTTATTTTTATTTTTATTTTTATTTTT"],"clinical_significance":[],"seq_region_name":"7","id":"rs766249808"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1186367147","feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140509696,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509696},{"seq_region_name":"7","id":"rs957173725","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509700,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140509700},{"clinical_significance":[],"seq_region_name":"7","id":"rs926740285","source":"dbSNP","start":140509703,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C","T"],"end":140509703,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1388585978","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509704,"feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140509704},{"id":"rs1795624019","seq_region_name":"7","clinical_significance":[],"start":140509707,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140509707,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140509709,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509709,"source":"dbSNP","id":"rs1795624037","seq_region_name":"7","clinical_significance":[]},{"id":"rs1212461914","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140509710,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509710,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140509715,"alleles":["TTTTTT","TTTTTTT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509710,"clinical_significance":[],"seq_region_name":"7","id":"rs1585526583"},{"seq_region_name":"7","id":"rs1795624090","clinical_significance":[],"end":140509711,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140509711,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140509715,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140509715,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795624111","clinical_significance":[]},{"source":"dbSNP","start":140509718,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140509718,"alleles":["A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs530338737","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509719,"feature_type":"variation","strand":1,"end":140509719,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795624149"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509720,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140509720,"clinical_significance":[],"seq_region_name":"7","id":"rs1465072756"},{"feature_type":"variation","strand":1,"end":140509722,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509722,"clinical_significance":[],"seq_region_name":"7","id":"rs2130428844"},{"end":140509723,"alleles":["G","A","C","T"],"strand":1,"feature_type":"variation","start":140509723,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs189329890","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs867227450","end":140509727,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140509727,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs756617345","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","C","T"],"end":140509728,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509728,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1368616875","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509729,"source":"dbSNP","strand":1,"feature_type":"variation","end":140509729,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs898011702","clinical_significance":[],"alleles":["T","C"],"end":140509730,"strand":1,"feature_type":"variation","start":140509730,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1325303724","seq_region_name":"7","source":"dbSNP","start":140509732,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140509732,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140509733,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509733,"clinical_significance":[],"seq_region_name":"7","id":"rs1585526602"},{"seq_region_name":"7","id":"rs1795624349","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","-"],"end":140509733,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509733,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509735,"feature_type":"variation","strand":1,"end":140509735,"alleles":["T","C"],"clinical_significance":[],"id":"rs1435895848","seq_region_name":"7"},{"seq_region_name":"7","id":"rs557613765","clinical_significance":[],"start":140509737,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C","G"],"end":140509737,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1585526607","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140509741,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509741,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140509742,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509742,"clinical_significance":[],"seq_region_name":"7","id":"rs1795624496"},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140509744,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509744,"source":"dbSNP","seq_region_name":"7","id":"rs1585526609","clinical_significance":[]},{"alleles":["A","G"],"end":140509748,"feature_type":"variation","strand":1,"source":"dbSNP","start":140509748,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585526612"},{"seq_region_name":"7","id":"rs1302759445","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509750,"source":"dbSNP","strand":1,"feature_type":"variation","end":140509750,"alleles":["T","G"]},{"source":"dbSNP","start":140509750,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TG","TGTG"],"end":140509751,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1465038848"},{"start":140509753,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140509753,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795624589","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1052447695","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509754,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140509754},{"feature_type":"variation","strand":1,"end":140509758,"alleles":["T","C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509758,"clinical_significance":[],"seq_region_name":"7","id":"rs1453545078"},{"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140509759,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509759,"source":"dbSNP","seq_region_name":"7","id":"rs1585526620","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509768,"feature_type":"variation","strand":1,"end":140509768,"alleles":["G","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs372583018"},{"end":140509769,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140509769,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1437728781","seq_region_name":"7"},{"id":"rs1795624704","seq_region_name":"7","clinical_significance":[],"end":140509771,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140509771,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795624716","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","-"],"end":140509771,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509771,"source":"dbSNP"},{"end":140509774,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140509774,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs560620930","clinical_significance":[]},{"alleles":["C","G"],"end":140509779,"strand":1,"feature_type":"variation","start":140509779,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795624759","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1017267138","alleles":["G","A","C"],"end":140509783,"feature_type":"variation","strand":1,"source":"dbSNP","start":140509783,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1585526637","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509784,"source":"dbSNP","strand":1,"feature_type":"variation","end":140509784,"alleles":["A","C"]},{"seq_region_name":"7","id":"rs904167423","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509785,"source":"dbSNP","strand":1,"feature_type":"variation","end":140509785,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1394938035","end":140509786,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140509786,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1192537954","source":"dbSNP","start":140509788,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140509788,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509789,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140509789,"clinical_significance":[],"seq_region_name":"7","id":"rs770452401"},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140509790,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509790,"clinical_significance":[],"id":"rs927016230","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509791,"feature_type":"variation","strand":1,"end":140509791,"alleles":["A","C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs191265698"},{"seq_region_name":"7","id":"rs1795624909","clinical_significance":[],"start":140509792,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140509792,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1202978296","seq_region_name":"7","source":"dbSNP","start":140509796,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140509796,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1485319790","clinical_significance":[],"alleles":["CC","CCC"],"end":140509801,"strand":1,"feature_type":"variation","start":140509800,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1795624955","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509801,"feature_type":"variation","strand":1,"end":140509801,"alleles":["C","A"]},{"seq_region_name":"7","id":"rs1795624977","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509805,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140509805},{"source":"dbSNP","start":140509806,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140509806,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1305084326"},{"end":140509814,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140509814,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs151073136","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1231818620","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509816,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140509816},{"end":140509818,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140509818,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795625070","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","A","C"],"end":140509821,"feature_type":"variation","strand":1,"source":"dbSNP","start":140509821,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs4354233","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs538709214","end":140509822,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140509822,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs550611564","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509837,"source":"dbSNP","strand":1,"feature_type":"variation","end":140509837,"alleles":["C","T"]},{"alleles":["G","T"],"end":140509839,"feature_type":"variation","strand":1,"source":"dbSNP","start":140509839,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795625379","seq_region_name":"7"},{"source":"dbSNP","start":140509842,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140509842,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs980761832"},{"end":140509843,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140509843,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs926643849","clinical_significance":[]},{"source":"dbSNP","start":140509844,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140509844,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs374536818","seq_region_name":"7"},{"alleles":["T","C"],"end":140509845,"strand":1,"feature_type":"variation","start":140509845,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1381885832","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509848,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140509848,"clinical_significance":[],"seq_region_name":"7","id":"rs1247158026"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509850,"feature_type":"variation","strand":1,"end":140509850,"alleles":["C","G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1380088067"},{"clinical_significance":[],"seq_region_name":"7","id":"rs536157752","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140509851,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509851},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795626473","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509853,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140509853},{"seq_region_name":"7","id":"rs1375435539","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509855,"source":"dbSNP","strand":1,"feature_type":"variation","end":140509855,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs183756320","feature_type":"variation","strand":1,"end":140509860,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509860},{"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140509871,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509871,"clinical_significance":[],"id":"rs923250494","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140509877,"alleles":["TTTTTT","TTTTTTT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509872,"clinical_significance":[],"seq_region_name":"7","id":"rs1194499794"},{"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140509873,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509873,"source":"dbSNP","seq_region_name":"7","id":"rs112590729","clinical_significance":[]},{"seq_region_name":"7","id":"rs533769819","clinical_significance":[],"end":140509878,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140509878,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140509880,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140509880,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1190318846"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1175365747","alleles":["AG","-"],"end":140509887,"feature_type":"variation","strand":1,"source":"dbSNP","start":140509886,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1427555425","alleles":["GGG","GG"],"end":140509889,"feature_type":"variation","strand":1,"source":"dbSNP","start":140509887,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795626775","clinical_significance":[],"start":140509893,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140509893,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509895,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140509895,"clinical_significance":[],"seq_region_name":"7","id":"rs1256412842"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140509896,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509896,"clinical_significance":[],"id":"rs2130429023","seq_region_name":"7"},{"seq_region_name":"7","id":"rs973466048","clinical_significance":[],"strand":1,"feature_type":"variation","end":140509897,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509897,"source":"dbSNP"},{"source":"dbSNP","start":140509900,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140509900,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795626973"},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140509901,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509901,"clinical_significance":[],"id":"rs1795627003","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509903,"feature_type":"variation","strand":1,"end":140509903,"alleles":["A","AA"],"clinical_significance":[],"seq_region_name":"7","id":"rs1189869050"},{"seq_region_name":"7","id":"rs1795627067","clinical_significance":[],"end":140509908,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140509908,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795627094","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140509909,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509909,"source":"dbSNP"},{"end":140509917,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140509917,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795627130"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1484554215","end":140509920,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140509920,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140509925,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140509925,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1279569222","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509926,"source":"dbSNP","strand":1,"feature_type":"variation","end":140509926,"alleles":["T","G"],"seq_region_name":"7","id":"rs1795627183","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795627205","source":"dbSNP","start":140509933,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140509933,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585526732","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140509937,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509937},{"start":140509938,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140509938,"alleles":["C","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795627239","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795627250","clinical_significance":[],"start":140509940,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140509940,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509941,"source":"dbSNP","strand":1,"feature_type":"variation","end":140509941,"alleles":["G","T"],"seq_region_name":"7","id":"rs1795627266","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795627284","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509942,"feature_type":"variation","strand":1,"end":140509942,"alleles":["C","T"]},{"source":"dbSNP","start":140509943,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140509943,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585526736"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795627331","source":"dbSNP","start":140509944,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140509944,"alleles":["T","C"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509945,"feature_type":"variation","strand":1,"end":140509945,"alleles":["C","G","T"],"clinical_significance":[],"id":"rs1364909649","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140509946,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509946,"source":"dbSNP","seq_region_name":"7","id":"rs188476101","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795627415","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509948,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140509948},{"alleles":["G","C"],"end":140509959,"strand":1,"feature_type":"variation","start":140509959,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795627435","clinical_significance":[]},{"clinical_significance":[],"id":"rs1249704674","seq_region_name":"7","end":140509963,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140509963,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140509966,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509966,"source":"dbSNP","seq_region_name":"7","id":"rs1795627486","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795627506","clinical_significance":[],"start":140509970,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140509970,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140509978,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509978,"source":"dbSNP","seq_region_name":"7","id":"rs919306899","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509981,"source":"dbSNP","strand":1,"feature_type":"variation","end":140509981,"alleles":["A","C"],"seq_region_name":"7","id":"rs1585526744","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509983,"source":"dbSNP","strand":1,"feature_type":"variation","end":140509983,"alleles":["C","G"],"id":"rs1795627560","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1226697428","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140509987,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509987,"source":"dbSNP"},{"end":140509989,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140509989,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs929502029"},{"feature_type":"variation","strand":1,"end":140509992,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140509992,"clinical_significance":[],"id":"rs2130429094","seq_region_name":"7"},{"id":"rs1051927765","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140509994,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509994,"source":"dbSNP"},{"source":"dbSNP","start":140509995,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140509995,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1295336839"},{"alleles":["T","C"],"end":140509996,"strand":1,"feature_type":"variation","start":140509996,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1413379431","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140509998,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140509998,"source":"dbSNP","seq_region_name":"7","id":"rs1795627671","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140510011,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510011,"clinical_significance":[],"seq_region_name":"7","id":"rs890729732"},{"alleles":["A","G"],"end":140510013,"strand":1,"feature_type":"variation","start":140510013,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2363821","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510017,"feature_type":"variation","strand":1,"end":140510017,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs867529392"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795627889","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510019,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140510019},{"source":"dbSNP","start":140510021,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140510021,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1039276720"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510024,"source":"dbSNP","strand":1,"feature_type":"variation","end":140510024,"alleles":["C","T"],"id":"rs1795627928","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130429126","feature_type":"variation","strand":1,"end":140510025,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510025},{"start":140510027,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G","T"],"end":140510027,"strand":1,"feature_type":"variation","id":"rs904199944","seq_region_name":"7","clinical_significance":[]},{"start":140510028,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C"],"end":140510028,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1461693587","clinical_significance":[]},{"source":"dbSNP","start":140510038,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C","G"],"end":140510038,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs892746244"},{"seq_region_name":"7","id":"rs1795628025","clinical_significance":[],"start":140510038,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140510043,"alleles":["TAAACC","TAAACCTAAACC"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs2130429138","seq_region_name":"7","source":"dbSNP","start":140510043,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140510043,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs181361700","clinical_significance":[],"end":140510046,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140510046,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510052,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140510052,"clinical_significance":[],"seq_region_name":"7","id":"rs1052895704"},{"alleles":["C","G"],"end":140510058,"feature_type":"variation","strand":1,"source":"dbSNP","start":140510058,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs540640732","seq_region_name":"7"},{"seq_region_name":"7","id":"rs2130429148","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510059,"source":"dbSNP","strand":1,"feature_type":"variation","end":140510059,"alleles":["A","G"]},{"start":140510062,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140510062,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585526787","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140510066,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510066,"source":"dbSNP","id":"rs1485552689","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510069,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140510069,"seq_region_name":"7","id":"rs971051064","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510070,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140510070,"clinical_significance":[],"seq_region_name":"7","id":"rs1795628189"},{"seq_region_name":"7","id":"rs1795628210","clinical_significance":[],"alleles":["T","G"],"end":140510071,"strand":1,"feature_type":"variation","start":140510071,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795628227","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510072,"feature_type":"variation","strand":1,"end":140510072,"alleles":["G","A"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510076,"source":"dbSNP","strand":1,"feature_type":"variation","end":140510076,"alleles":["C","A"],"seq_region_name":"7","id":"rs1795628249","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140510077,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510077,"source":"dbSNP","seq_region_name":"7","id":"rs1585526792","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510079,"feature_type":"variation","strand":1,"end":140510079,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795628282"},{"seq_region_name":"7","id":"rs1795628305","clinical_significance":[],"alleles":["T","C"],"end":140510084,"strand":1,"feature_type":"variation","start":140510084,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510085,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140510085,"seq_region_name":"7","id":"rs1337515325","clinical_significance":[]},{"source":"dbSNP","start":140510087,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140510087,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs140083811"},{"id":"rs1248324489","seq_region_name":"7","clinical_significance":[],"start":140510092,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C","T"],"end":140510092,"strand":1,"feature_type":"variation"},{"start":140510096,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140510096,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1195361592","clinical_significance":[]},{"end":140510101,"alleles":["TTTT","TTT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140510098,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1267339588"},{"start":140510102,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140510102,"strand":1,"feature_type":"variation","id":"rs1795628451","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795628464","alleles":["C","T"],"end":140510104,"feature_type":"variation","strand":1,"source":"dbSNP","start":140510104,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140510108,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510108,"clinical_significance":[],"seq_region_name":"7","id":"rs1357121430"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1275329114","source":"dbSNP","start":140510109,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140510109,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs764428903","clinical_significance":[],"end":140510110,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140510110,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1024126026","clinical_significance":[],"end":140510115,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140510115,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795628573","clinical_significance":[],"alleles":["CAATCA","CA"],"end":140510121,"strand":1,"feature_type":"variation","start":140510116,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510119,"feature_type":"variation","strand":1,"end":140510119,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795628590"},{"seq_region_name":"7","id":"rs1795628615","clinical_significance":[],"strand":1,"feature_type":"variation","end":140510123,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510123,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130429191","source":"dbSNP","start":140510129,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140510129,"feature_type":"variation","strand":1},{"id":"rs1034065681","seq_region_name":"7","clinical_significance":[],"end":140510130,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140510130,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140510133,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140510133,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795628658"},{"start":140510140,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140510140,"strand":1,"feature_type":"variation","id":"rs1335222140","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs6945832","clinical_significance":[],"strand":1,"feature_type":"variation","end":140510141,"alleles":["G","A","C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510141,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795628889","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510142,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140510142},{"end":140510146,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140510146,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795628920","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140510147,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510147,"clinical_significance":[],"id":"rs1264118840","seq_region_name":"7"},{"end":140510149,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140510149,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1001418437","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795628976","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510151,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140510151},{"start":140510155,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140510155,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585526832","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140510168,"alleles":["TTTTTTTTTTTTT","TTTTTTTTTT","TTTTTTTTTTT","TTTTTTTTTTTT","TTTTTTTTTTTTTT","TTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510156,"clinical_significance":[],"seq_region_name":"7","id":"rs61572645"},{"clinical_significance":[],"id":"rs1795629110","seq_region_name":"7","end":140510158,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140510158,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140510163,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140510163,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1267461036","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs996988176","alleles":["G","A","T"],"end":140510169,"feature_type":"variation","strand":1,"source":"dbSNP","start":140510169,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795629178","source":"dbSNP","start":140510169,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","-"],"end":140510169,"feature_type":"variation","strand":1},{"end":140510171,"alleles":["GAG","-"],"strand":1,"feature_type":"variation","start":140510169,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1487604252","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130429253","clinical_significance":[],"strand":1,"feature_type":"variation","end":140510171,"alleles":["G","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510171,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1251300884","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["-","TTTT"],"end":140510171,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510172,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510172,"feature_type":"variation","strand":1,"end":140510172,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795629242"},{"source":"dbSNP","start":140510174,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140510174,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1473896941"},{"clinical_significance":[],"id":"rs1180633950","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510176,"feature_type":"variation","strand":1,"alleles":["-","TTTTTTT"],"end":140510175},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140510177,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510177,"source":"dbSNP","id":"rs1416626265","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1158999202","feature_type":"variation","strand":1,"end":140510186,"alleles":["CTCT","CT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510183},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510187,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140510187,"seq_region_name":"7","id":"rs1795629316","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1016770466","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140510189,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510189},{"clinical_significance":[],"seq_region_name":"7","id":"rs541848675","feature_type":"variation","strand":1,"end":140510190,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510190},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510191,"feature_type":"variation","strand":1,"end":140510191,"alleles":["C","T"],"clinical_significance":[],"id":"rs1795629392","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140510193,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510193,"clinical_significance":[],"seq_region_name":"7","id":"rs1180964808"},{"alleles":["C","T"],"end":140510197,"feature_type":"variation","strand":1,"source":"dbSNP","start":140510197,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795629437"},{"seq_region_name":"7","id":"rs1468830600","clinical_significance":[],"strand":1,"feature_type":"variation","end":140510200,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510200,"source":"dbSNP"},{"source":"dbSNP","start":140510203,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140510203,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585526873"},{"seq_region_name":"7","id":"rs1254992075","clinical_significance":[],"start":140510206,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140510206,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1795629513","clinical_significance":[],"end":140510208,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140510208,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs111735625","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140510210,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510210,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1468254469","end":140510211,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140510211,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795629588","feature_type":"variation","strand":1,"end":140510213,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510213},{"clinical_significance":[],"seq_region_name":"7","id":"rs377238856","source":"dbSNP","start":140510214,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140510214,"alleles":["A","G"],"feature_type":"variation","strand":1},{"start":140510217,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","G"],"end":140510217,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs973372788","clinical_significance":[]},{"seq_region_name":"7","id":"rs1225879061","clinical_significance":[],"alleles":["C","A"],"end":140510219,"strand":1,"feature_type":"variation","start":140510219,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140510220,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140510220,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795629669","clinical_significance":[]},{"start":140510229,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140510229,"alleles":["C","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1167302740","clinical_significance":[]},{"alleles":["C","A"],"end":140510232,"feature_type":"variation","strand":1,"source":"dbSNP","start":140510232,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1279294943"},{"alleles":["C","T"],"end":140510233,"strand":1,"feature_type":"variation","start":140510233,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs919369619","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795629748","clinical_significance":[],"alleles":["T","G"],"end":140510236,"strand":1,"feature_type":"variation","start":140510236,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795629760","clinical_significance":[],"strand":1,"feature_type":"variation","end":140510239,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510239,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795629783","source":"dbSNP","start":140510242,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140510242,"alleles":["C","T"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140510243,"alleles":["C","A","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510243,"source":"dbSNP","id":"rs143768419","seq_region_name":"7","clinical_significance":[]},{"id":"rs367634469","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510244,"source":"dbSNP","strand":1,"feature_type":"variation","end":140510244,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs546440097","clinical_significance":[],"start":140510246,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140510246,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1298288672","feature_type":"variation","strand":1,"end":140510251,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510251},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510253,"feature_type":"variation","strand":1,"end":140510253,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795629914"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510257,"source":"dbSNP","strand":1,"feature_type":"variation","end":140510257,"alleles":["T","A"],"seq_region_name":"7","id":"rs1795629927","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510258,"source":"dbSNP","strand":1,"feature_type":"variation","end":140510258,"alleles":["C","T"],"seq_region_name":"7","id":"rs1585526907","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140510263,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510263,"source":"dbSNP","id":"rs1318544736","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs2130429333","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510270,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140510270},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140510271,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510271,"clinical_significance":[],"seq_region_name":"7","id":"rs1795629955"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795629976","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140510275,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510275},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510279,"feature_type":"variation","strand":1,"end":140510279,"alleles":["T","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs962013246"},{"seq_region_name":"7","id":"rs34739734","clinical_significance":[],"start":140510283,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140510285,"alleles":["GGG","GGGG"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1382553418","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140510284,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510284,"source":"dbSNP"},{"id":"rs988067924","seq_region_name":"7","clinical_significance":[],"start":140510285,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140510285,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1157735555","seq_region_name":"7","feature_type":"variation","strand":1,"end":140510286,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510286},{"clinical_significance":[],"id":"rs1183246338","seq_region_name":"7","feature_type":"variation","strand":1,"end":140510287,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510287},{"feature_type":"variation","strand":1,"end":140510292,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510292,"clinical_significance":[],"seq_region_name":"7","id":"rs1407979222"},{"seq_region_name":"7","id":"rs1795630117","clinical_significance":[],"alleles":["GG","G"],"end":140510293,"strand":1,"feature_type":"variation","start":140510292,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs912077820","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510296,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140510296},{"id":"rs1396803664","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510300,"source":"dbSNP","strand":1,"feature_type":"variation","end":140510300,"alleles":["C","T"]},{"id":"rs1191888094","seq_region_name":"7","clinical_significance":[],"alleles":["C","A"],"end":140510301,"strand":1,"feature_type":"variation","start":140510301,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140510305,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140510305,"alleles":["A","C"],"strand":1,"feature_type":"variation","id":"rs2130429362","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795630176","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510306,"source":"dbSNP","strand":1,"feature_type":"variation","end":140510306,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1287661694","source":"dbSNP","start":140510307,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140510307,"alleles":["G","A"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140510308,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140510308,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795630215"},{"alleles":["C","A","T"],"end":140510310,"feature_type":"variation","strand":1,"source":"dbSNP","start":140510310,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs61174733","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795630385","source":"dbSNP","start":140510311,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140510311,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs146848126","clinical_significance":[],"start":140510313,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C","T"],"end":140510313,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1218248973","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510329,"feature_type":"variation","strand":1,"end":140510329,"alleles":["C","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510336,"source":"dbSNP","strand":1,"feature_type":"variation","end":140510336,"alleles":["G","A"],"seq_region_name":"7","id":"rs1445444679","clinical_significance":[]},{"seq_region_name":"7","id":"rs1039306337","clinical_significance":[],"alleles":["C","T"],"end":140510338,"strand":1,"feature_type":"variation","start":140510338,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140510339,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C"],"end":140510339,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs765531110","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795630530","clinical_significance":[],"start":140510340,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140510340,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"start":140510341,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["GGG","GG"],"end":140510343,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795630546","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510342,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140510342,"clinical_significance":[],"seq_region_name":"7","id":"rs1795630563"},{"feature_type":"variation","strand":1,"end":140510343,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510343,"clinical_significance":[],"seq_region_name":"7","id":"rs2130429399"},{"strand":1,"feature_type":"variation","end":140510344,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510344,"source":"dbSNP","seq_region_name":"7","id":"rs1585526925","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130429407","clinical_significance":[],"start":140510346,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140510346,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140510350,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510350,"clinical_significance":[],"seq_region_name":"7","id":"rs1795630591"},{"start":140510351,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140510351,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs935689288","clinical_significance":[]},{"seq_region_name":"7","id":"rs1320187510","clinical_significance":[],"end":140510353,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140510353,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140510355,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140510355,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795630643"},{"start":140510357,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140510357,"strand":1,"feature_type":"variation","id":"rs1795630661","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1052776200","clinical_significance":[],"alleles":["C","A"],"end":140510362,"strand":1,"feature_type":"variation","start":140510362,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs933318016","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140510364,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510364},{"seq_region_name":"7","id":"rs1278798031","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510365,"source":"dbSNP","strand":1,"feature_type":"variation","end":140510365,"alleles":["G","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130429428","end":140510367,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140510367,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140510369,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510369,"source":"dbSNP","seq_region_name":"7","id":"rs1795630743","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795630761","clinical_significance":[],"start":140510372,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140510372,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140510373,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140510373,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1231505865","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795630795","feature_type":"variation","strand":1,"end":140510375,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510375},{"feature_type":"variation","strand":1,"end":140510379,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510379,"clinical_significance":[],"id":"rs1585526939","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510380,"feature_type":"variation","strand":1,"end":140510380,"alleles":["C","T"],"clinical_significance":[],"id":"rs2130429442","seq_region_name":"7"},{"end":140510383,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140510383,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795630835","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795630857","clinical_significance":[],"alleles":["A","G"],"end":140510384,"strand":1,"feature_type":"variation","start":140510384,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130429448","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510385,"feature_type":"variation","strand":1,"alleles":["-","AG"],"end":140510384},{"id":"rs1252025675","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510385,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140510385},{"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140510387,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510387,"source":"dbSNP","id":"rs1484084956","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140510389,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140510389,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1203033278"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1251773446","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510394,"feature_type":"variation","strand":1,"end":140510394,"alleles":["C","T"]},{"start":140510395,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140510395,"strand":1,"feature_type":"variation","id":"rs1585526953","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140510397,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510397,"clinical_significance":[],"seq_region_name":"7","id":"rs1795630984"},{"source":"dbSNP","start":140510399,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140510399,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs532254478"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585526958","alleles":["T","C"],"end":140510404,"feature_type":"variation","strand":1,"source":"dbSNP","start":140510404,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1585526960","seq_region_name":"7","clinical_significance":[],"alleles":["A","C"],"end":140510408,"strand":1,"feature_type":"variation","start":140510408,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510409,"source":"dbSNP","strand":1,"feature_type":"variation","end":140510409,"alleles":["A","G"],"seq_region_name":"7","id":"rs1795631057","clinical_significance":[]},{"seq_region_name":"7","id":"rs891564177","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510411,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140510411},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510412,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140510412,"clinical_significance":[],"seq_region_name":"7","id":"rs1795631174"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1014021162","alleles":["G","A"],"end":140510413,"feature_type":"variation","strand":1,"source":"dbSNP","start":140510413,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510417,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140510417,"clinical_significance":[],"seq_region_name":"7","id":"rs1585526965"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140510418,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510418,"clinical_significance":[],"id":"rs1795631234","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795631247","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510419,"source":"dbSNP","strand":1,"feature_type":"variation","end":140510419,"alleles":["A","T"]},{"start":140510423,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140510423,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1324265271","clinical_significance":[]},{"source":"dbSNP","start":140510427,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A","G"],"end":140510427,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1585526969","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140510430,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510430,"source":"dbSNP","id":"rs1795631296","seq_region_name":"7","clinical_significance":[]},{"start":140510431,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140510431,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130429491","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140510432,"alleles":["G","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510432,"clinical_significance":[],"id":"rs1585526971","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795631331","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510434,"feature_type":"variation","strand":1,"alleles":["-","GGTG"],"end":140510433},{"seq_region_name":"7","id":"rs1045862116","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510437,"source":"dbSNP","strand":1,"feature_type":"variation","end":140510437,"alleles":["C","A","T"]},{"clinical_significance":[],"id":"rs905701620","seq_region_name":"7","feature_type":"variation","strand":1,"end":140510438,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510438},{"clinical_significance":[],"seq_region_name":"7","id":"rs1171645672","alleles":["T","A","C"],"end":140510439,"feature_type":"variation","strand":1,"source":"dbSNP","start":140510439,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795631432","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140510440,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510440,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140510441,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510441,"clinical_significance":[],"seq_region_name":"7","id":"rs1795631456"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795631471","source":"dbSNP","start":140510443,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140510443,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140510445,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140510445,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs771702674","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1420342197","end":140510446,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140510446,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1795631513","seq_region_name":"7","source":"dbSNP","start":140510446,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140510447,"alleles":["CC","CCC"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1795631532","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140510449,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510449},{"start":140510452,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140510452,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs1585526991","seq_region_name":"7","clinical_significance":[]},{"id":"rs1795631574","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140510453,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510453,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1188296520","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510456,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140510456},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563108958","source":"dbSNP","start":140510457,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TTTTTT","TTTTT","TTTTTTT"],"end":140510462,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510458,"source":"dbSNP","strand":1,"feature_type":"variation","end":140510458,"alleles":["T","C"],"seq_region_name":"7","id":"rs892645298","clinical_significance":[]},{"source":"dbSNP","start":140510462,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140510462,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795631666"},{"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140510463,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510463,"clinical_significance":[],"id":"rs1001281636","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1241740789","end":140510469,"alleles":["AAAAAAA","AAAAAAAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140510463,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510470,"feature_type":"variation","strand":1,"end":140510470,"alleles":["T","A"],"clinical_significance":[],"id":"rs1486846007","seq_region_name":"7"},{"id":"rs1585527003","seq_region_name":"7","clinical_significance":[],"end":140510475,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140510475,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1412031629","alleles":["C","A","T"],"end":140510486,"feature_type":"variation","strand":1,"source":"dbSNP","start":140510486,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1016845703","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140510488,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510488,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1795631797","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140510490,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510490},{"source":"dbSNP","start":140510492,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140510495,"alleles":["TCAT","TCATCAT"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1210838783"},{"feature_type":"variation","strand":1,"end":140510497,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510497,"clinical_significance":[],"seq_region_name":"7","id":"rs1273117225"},{"start":140510497,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["CC","C"],"end":140510498,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1308551400","clinical_significance":[]},{"start":140510498,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140510498,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs1215750826","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1337100341","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510499,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140510499},{"id":"rs2130429569","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140510504,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510504,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795631904","alleles":["C","T"],"end":140510507,"feature_type":"variation","strand":1,"source":"dbSNP","start":140510507,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140510510,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140510510,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1422944943","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795631954","end":140510513,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140510513,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs112448024","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510514,"source":"dbSNP","strand":1,"feature_type":"variation","end":140510514,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1795631995","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510515,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140510515},{"seq_region_name":"7","id":"rs962594532","clinical_significance":[],"start":140510516,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140510516,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140510518,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510518,"source":"dbSNP","id":"rs1415209104","seq_region_name":"7","clinical_significance":[]},{"end":140510520,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140510520,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1357166854","clinical_significance":[]},{"end":140510523,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140510523,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795632090","clinical_significance":[]},{"source":"dbSNP","start":140510526,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140510526,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1009662006"},{"clinical_significance":[],"id":"rs1391567665","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140510533,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510533},{"id":"rs758488222","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510538,"source":"dbSNP","strand":1,"feature_type":"variation","end":140510538,"alleles":["G","C"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510544,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140510544,"seq_region_name":"7","id":"rs2130429600","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585527041","end":140510546,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140510546,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130429605","end":140510547,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140510547,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140510553,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510553,"source":"dbSNP","seq_region_name":"7","id":"rs372216448","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510554,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140510554,"seq_region_name":"7","id":"rs1427264088","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140510556,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510556,"source":"dbSNP","seq_region_name":"7","id":"rs1306829205","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1046638122","source":"dbSNP","start":140510560,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140510560,"feature_type":"variation","strand":1},{"start":140510561,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140510561,"alleles":["A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130429614","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795632251","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140510562,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510562,"source":"dbSNP"},{"seq_region_name":"7","id":"rs186644859","clinical_significance":[],"alleles":["G","C"],"end":140510567,"strand":1,"feature_type":"variation","start":140510567,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140510568,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510568,"source":"dbSNP","seq_region_name":"7","id":"rs752699043","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140510569,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510569,"clinical_significance":[],"seq_region_name":"7","id":"rs1795632329"},{"feature_type":"variation","strand":1,"end":140510574,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510574,"clinical_significance":[],"id":"rs1795632356","seq_region_name":"7"},{"start":140510576,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140510576,"strand":1,"feature_type":"variation","id":"rs755925278","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795632397","clinical_significance":[],"strand":1,"feature_type":"variation","end":140510580,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510580,"source":"dbSNP"},{"id":"rs1408264364","seq_region_name":"7","clinical_significance":[],"start":140510586,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140510586,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510595,"feature_type":"variation","strand":1,"end":140510595,"alleles":["T","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1419137229"},{"end":140510596,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140510596,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795632460","clinical_significance":[]},{"source":"dbSNP","start":140510597,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140510597,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795632481"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795632497","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510600,"feature_type":"variation","strand":1,"end":140510600,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs1585527065","clinical_significance":[],"end":140510610,"alleles":["T","C","G"],"strand":1,"feature_type":"variation","start":140510610,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510613,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140510613,"seq_region_name":"7","id":"rs189863110","clinical_significance":[]},{"end":140510618,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140510618,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795632565"},{"clinical_significance":[],"id":"rs1795632580","seq_region_name":"7","end":140510621,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140510621,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510622,"source":"dbSNP","strand":1,"feature_type":"variation","end":140510622,"alleles":["G","A"],"id":"rs1795632595","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs777478695","source":"dbSNP","start":140510623,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140510623,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140510626,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510626,"source":"dbSNP","seq_region_name":"7","id":"rs547879099","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs7455575","source":"dbSNP","start":140510627,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140510627,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795632742","alleles":["A","G"],"end":140510629,"feature_type":"variation","strand":1,"source":"dbSNP","start":140510629,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs756818993","clinical_significance":[],"alleles":["C","T"],"end":140510630,"strand":1,"feature_type":"variation","start":140510630,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140510631,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510631,"clinical_significance":[],"seq_region_name":"7","id":"rs974902315"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130429664","end":140510634,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140510634,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510637,"feature_type":"variation","strand":1,"end":140510637,"alleles":["A","C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs926223275"},{"clinical_significance":[],"id":"rs958511858","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510641,"feature_type":"variation","strand":1,"end":140510641,"alleles":["C","A"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510648,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140510648,"clinical_significance":[],"id":"rs1795632862","seq_region_name":"7"},{"alleles":["G","T"],"end":140510651,"feature_type":"variation","strand":1,"source":"dbSNP","start":140510651,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1563108986","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140510659,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510659,"clinical_significance":[],"id":"rs59098044","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140510661,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510661,"clinical_significance":[],"seq_region_name":"7","id":"rs1795632914"},{"seq_region_name":"7","id":"rs61664951","clinical_significance":[],"start":140510662,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C"],"end":140510662,"strand":1,"feature_type":"variation"},{"id":"rs1006367270","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140510665,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510665,"source":"dbSNP"},{"id":"rs936220873","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140510669,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510669,"source":"dbSNP"},{"id":"rs1053757839","seq_region_name":"7","clinical_significance":[],"start":140510675,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140510675,"strand":1,"feature_type":"variation"},{"start":140510676,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140510676,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs912908802","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140510677,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510677,"source":"dbSNP","seq_region_name":"7","id":"rs1795633043","clinical_significance":[]},{"source":"dbSNP","start":140510680,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140510680,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795633065"},{"start":140510681,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140510681,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795633080","clinical_significance":[]},{"clinical_significance":[],"id":"rs2130429711","seq_region_name":"7","feature_type":"variation","strand":1,"end":140510682,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510682},{"feature_type":"variation","strand":1,"end":140510684,"alleles":["G","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510684,"clinical_significance":[],"id":"rs1795633101","seq_region_name":"7"},{"seq_region_name":"7","id":"rs2130429716","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510685,"source":"dbSNP","strand":1,"feature_type":"variation","end":140510685,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585527093","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140510689,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510689},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140510690,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510690,"clinical_significance":[],"seq_region_name":"7","id":"rs1585527097"},{"seq_region_name":"7","id":"rs1585527101","clinical_significance":[],"start":140510695,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140510695,"strand":1,"feature_type":"variation"},{"start":140510700,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140510700,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs56372576","clinical_significance":[]},{"source":"dbSNP","start":140510704,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140510704,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795633185","seq_region_name":"7"},{"start":140510706,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140510706,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130429730","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795633200","clinical_significance":[],"strand":1,"feature_type":"variation","end":140510712,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510712,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140510716,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510716,"source":"dbSNP","seq_region_name":"7","id":"rs1291227018","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510717,"source":"dbSNP","strand":1,"feature_type":"variation","end":140510717,"alleles":["C","T"],"seq_region_name":"7","id":"rs1227519573","clinical_significance":[]},{"start":140510718,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140510718,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1374052757","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1299782343","feature_type":"variation","strand":1,"end":140510719,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510719},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795633296","feature_type":"variation","strand":1,"end":140510720,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510720},{"seq_region_name":"7","id":"rs949716039","clinical_significance":[],"end":140510721,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140510721,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["C","G"],"end":140510730,"strand":1,"feature_type":"variation","start":140510730,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795633337","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs971859268","seq_region_name":"7","source":"dbSNP","start":140510731,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140510731,"alleles":["C","G"],"feature_type":"variation","strand":1},{"id":"rs547859457","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140510732,"strand":1,"feature_type":"variation","start":140510732,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510733,"feature_type":"variation","strand":1,"end":140510733,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1273985778"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510734,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140510734,"clinical_significance":[],"seq_region_name":"7","id":"rs1486306483"},{"alleles":["G","C"],"end":140510735,"feature_type":"variation","strand":1,"source":"dbSNP","start":140510735,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1212850484"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510736,"source":"dbSNP","strand":1,"feature_type":"variation","end":140510736,"alleles":["C","T"],"seq_region_name":"7","id":"rs1795633468","clinical_significance":[]},{"source":"dbSNP","start":140510740,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","AA"],"end":140510740,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1236141407","seq_region_name":"7"},{"source":"dbSNP","start":140510741,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140510741,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795633487"},{"clinical_significance":[],"id":"rs1483133671","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140510744,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510744},{"clinical_significance":[],"seq_region_name":"7","id":"rs1187404797","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140510747,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510747},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795633577","alleles":["C","A"],"end":140510751,"feature_type":"variation","strand":1,"source":"dbSNP","start":140510751,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140510752,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140510752,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs566455729","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs923221066","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510753,"feature_type":"variation","strand":1,"end":140510753,"alleles":["A","C"]},{"end":140510757,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140510757,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1420021409","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1410870033","clinical_significance":[],"start":140510763,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140510763,"alleles":["G","A","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1795633674","clinical_significance":[],"start":140510765,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140510765,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1045486566","end":140510769,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140510769,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs905614851","source":"dbSNP","start":140510777,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140510777,"alleles":["A","G","T"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510780,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140510780,"clinical_significance":[],"seq_region_name":"7","id":"rs1795633737"},{"strand":1,"feature_type":"variation","end":140510781,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510781,"source":"dbSNP","seq_region_name":"7","id":"rs1167467613","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795633780","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140510783,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510783},{"start":140510786,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140510786,"strand":1,"feature_type":"variation","id":"rs1795633801","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510787,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140510787,"clinical_significance":[],"id":"rs1795633819","seq_region_name":"7"},{"seq_region_name":"7","id":"rs2130429809","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510788,"source":"dbSNP","strand":1,"feature_type":"variation","end":140510788,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs937209202","source":"dbSNP","start":140510790,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140510790,"feature_type":"variation","strand":1},{"end":140510792,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140510792,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1395158256"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510793,"source":"dbSNP","strand":1,"feature_type":"variation","end":140510793,"alleles":["A","C","G"],"seq_region_name":"7","id":"rs530580199","clinical_significance":[]},{"start":140510794,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140510794,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795633928","clinical_significance":[]},{"id":"rs1220603685","seq_region_name":"7","clinical_significance":[],"end":140510795,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140510795,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795633968","source":"dbSNP","start":140510797,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140510797,"alleles":["A","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795633996","source":"dbSNP","start":140510802,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140510802,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510807,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140510807,"clinical_significance":[],"seq_region_name":"7","id":"rs1317268768"},{"end":140510808,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140510808,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs898440627","clinical_significance":[]},{"alleles":["C","T"],"end":140510809,"feature_type":"variation","strand":1,"source":"dbSNP","start":140510809,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1358439964"},{"source":"dbSNP","start":140510812,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140510812,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795634128"},{"start":140510814,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140510814,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs112644220","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795634194","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510817,"feature_type":"variation","strand":1,"end":140510817,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs745316560","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510819,"source":"dbSNP","strand":1,"feature_type":"variation","end":140510819,"alleles":["C","G","T"]},{"start":140510820,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140510820,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs1375969721","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140510821,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140510821,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1322247745","seq_region_name":"7"},{"id":"rs1443175026","seq_region_name":"7","clinical_significance":[],"start":140510823,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C"],"end":140510823,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs140694801","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510824,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140510824},{"clinical_significance":[],"seq_region_name":"7","id":"rs1433133846","end":140510828,"alleles":["GGG","GG"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140510826,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140510831,"alleles":["G","A","C","T"],"strand":1,"feature_type":"variation","start":140510831,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs113518986","clinical_significance":[]},{"end":140510833,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140510833,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs886444321"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510843,"feature_type":"variation","strand":1,"end":140510843,"alleles":["T","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795634535"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795634564","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510847,"feature_type":"variation","strand":1,"end":140510847,"alleles":["G","A","T"]},{"strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140510850,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510850,"source":"dbSNP","seq_region_name":"7","id":"rs1157295682","clinical_significance":[]},{"seq_region_name":"7","id":"rs1009311039","clinical_significance":[],"strand":1,"feature_type":"variation","end":140510852,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510852,"source":"dbSNP"},{"source":"dbSNP","start":140510853,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140510853,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1019062896"},{"strand":1,"feature_type":"variation","end":140510854,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510854,"source":"dbSNP","seq_region_name":"7","id":"rs910522961","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140510868,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510868,"source":"dbSNP","seq_region_name":"7","id":"rs1795634697","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140510870,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510870,"clinical_significance":[],"seq_region_name":"7","id":"rs964779869"},{"seq_region_name":"7","id":"rs764297500","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510871,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140510871},{"clinical_significance":[],"id":"rs1795634797","seq_region_name":"7","source":"dbSNP","start":140510873,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140510873,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510880,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140510880,"clinical_significance":[],"seq_region_name":"7","id":"rs1250805325"},{"seq_region_name":"7","id":"rs1795634845","clinical_significance":[],"alleles":["C","T"],"end":140510886,"strand":1,"feature_type":"variation","start":140510886,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1312083130","seq_region_name":"7","alleles":["C","T"],"end":140510891,"feature_type":"variation","strand":1,"source":"dbSNP","start":140510891,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1657556439","feature_type":"variation","strand":1,"end":140510892,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510892},{"seq_region_name":"7","id":"rs1795634912","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510897,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140510897},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130429881","source":"dbSNP","start":140510900,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140510900,"feature_type":"variation","strand":1},{"end":140510910,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140510910,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795634933","seq_region_name":"7"},{"start":140510911,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140510911,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795634961","clinical_significance":[]},{"seq_region_name":"7","id":"rs1033198302","clinical_significance":[],"alleles":["C","A","T"],"end":140510914,"strand":1,"feature_type":"variation","start":140510914,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs866793706","clinical_significance":[],"start":140510915,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140510915,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140510917,"alleles":["GTG","GTGTG"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510915,"source":"dbSNP","seq_region_name":"7","id":"rs1485966797","clinical_significance":[]},{"seq_region_name":"7","id":"rs1352966483","clinical_significance":[],"strand":1,"feature_type":"variation","end":140510916,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510916,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1280944257","clinical_significance":[],"alleles":["G","A"],"end":140510918,"strand":1,"feature_type":"variation","start":140510918,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795635145","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140510920,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510920},{"clinical_significance":[],"seq_region_name":"7","id":"rs1236660336","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140510921,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510921},{"clinical_significance":[],"id":"rs1795635194","seq_region_name":"7","feature_type":"variation","strand":1,"end":140510925,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510925},{"end":140510926,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140510926,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs182023627","seq_region_name":"7"},{"end":140510928,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140510928,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1300633847","seq_region_name":"7","clinical_significance":[]},{"end":140510929,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140510929,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1382997916","clinical_significance":[]},{"alleles":["G","A","C"],"end":140510931,"feature_type":"variation","strand":1,"source":"dbSNP","start":140510931,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1187527170"},{"seq_region_name":"7","id":"rs1253180304","clinical_significance":[],"alleles":["AATC","-"],"end":140510936,"strand":1,"feature_type":"variation","start":140510933,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1376636997","seq_region_name":"7","source":"dbSNP","start":140510935,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140510935,"alleles":["T","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795635440","feature_type":"variation","strand":1,"end":140510937,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510937},{"seq_region_name":"7","id":"rs1795635468","clinical_significance":[],"strand":1,"feature_type":"variation","end":140510938,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510938,"source":"dbSNP"},{"id":"rs1176053574","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140510945,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510945,"source":"dbSNP"},{"start":140510950,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140510950,"alleles":["A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs186294066","clinical_significance":[]},{"end":140510952,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140510952,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1188913023","clinical_significance":[]},{"start":140510958,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["-","ACTACAGGCGCACTCCACCAC"],"end":140510957,"strand":1,"feature_type":"variation","id":"rs1795635600","seq_region_name":"7","clinical_significance":[]},{"id":"rs1392756341","seq_region_name":"7","clinical_significance":[],"start":140510961,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140510961,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs945551115","source":"dbSNP","start":140510964,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140510964,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1428757331","alleles":["A","G"],"end":140510969,"feature_type":"variation","strand":1,"source":"dbSNP","start":140510969,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510973,"source":"dbSNP","strand":1,"feature_type":"variation","end":140510973,"alleles":["G","A","C"],"seq_region_name":"7","id":"rs1795635710","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585527198","clinical_significance":[],"start":140510975,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140510975,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140510976,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140510976,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795635770"},{"alleles":["C","A","T"],"end":140510977,"feature_type":"variation","strand":1,"source":"dbSNP","start":140510977,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs372233671","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140510978,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510978,"clinical_significance":[],"id":"rs1401198930","seq_region_name":"7"},{"clinical_significance":[],"id":"rs949783836","seq_region_name":"7","end":140510979,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140510979,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795635895","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140510981,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510981},{"source":"dbSNP","start":140510985,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140510985,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs546714405"},{"clinical_significance":[],"seq_region_name":"7","id":"rs542020245","feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140510986,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510986},{"clinical_significance":[],"id":"rs1795636017","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140510989,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140510989},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140510990,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140510990,"id":"rs1795636044","seq_region_name":"7","clinical_significance":[]},{"id":"rs1795636076","seq_region_name":"7","clinical_significance":[],"start":140510994,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140510994,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1563109067","clinical_significance":[],"start":140510996,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140510996,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511002,"feature_type":"variation","strand":1,"end":140511002,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795636130"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511003,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140511003,"seq_region_name":"7","id":"rs2130429968","clinical_significance":[]},{"seq_region_name":"7","id":"rs145459168","clinical_significance":[],"strand":1,"feature_type":"variation","end":140511008,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511008,"source":"dbSNP"},{"seq_region_name":"7","id":"rs78430939","clinical_significance":[],"alleles":["G","A","T"],"end":140511009,"strand":1,"feature_type":"variation","start":140511009,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1320153257","clinical_significance":[],"start":140511010,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140511010,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"id":"rs938253506","seq_region_name":"7","clinical_significance":[],"start":140511011,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140511011,"alleles":["G","A","C"],"strand":1,"feature_type":"variation"},{"start":140511015,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140511015,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795636416","clinical_significance":[]},{"alleles":["C","T"],"end":140511018,"strand":1,"feature_type":"variation","start":140511018,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1038061086","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs898343823","source":"dbSNP","start":140511019,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C","T"],"end":140511019,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs929760525","source":"dbSNP","start":140511020,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140511020,"feature_type":"variation","strand":1},{"end":140511022,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140511022,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795636534"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511026,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","G"],"end":140511026,"seq_region_name":"7","id":"rs1315128695","clinical_significance":[]},{"source":"dbSNP","start":140511032,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140511032,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs200548024"},{"feature_type":"variation","strand":1,"end":140511034,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511034,"clinical_significance":[],"seq_region_name":"7","id":"rs1273101683"},{"seq_region_name":"7","id":"rs1171543317","clinical_significance":[],"start":140511035,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140511035,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795636704","source":"dbSNP","start":140511038,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140511038,"feature_type":"variation","strand":1},{"id":"rs572791154","seq_region_name":"7","clinical_significance":[],"end":140511041,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140511041,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1008930660","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511042,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140511042},{"feature_type":"variation","strand":1,"end":140511046,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511046,"clinical_significance":[],"id":"rs191224207","seq_region_name":"7"},{"seq_region_name":"7","id":"rs112760559","clinical_significance":[],"start":140511047,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A","C","G"],"end":140511047,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511049,"source":"dbSNP","strand":1,"feature_type":"variation","end":140511049,"alleles":["T","G"],"seq_region_name":"7","id":"rs2130430019","clinical_significance":[]},{"id":"rs1563109088","seq_region_name":"7","clinical_significance":[],"start":140511052,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140511052,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"alleles":["C","G"],"end":140511054,"feature_type":"variation","strand":1,"source":"dbSNP","start":140511054,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795636863","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795636896","clinical_significance":[],"strand":1,"feature_type":"variation","end":140511056,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511056,"source":"dbSNP"},{"id":"rs1189733634","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["AAATAAATAAATAAATAAATAAA","AAATAAATAAATAAA","AAATAAATAAATAAATAAA","AAATAAATAAATAAATAAATAAATAAA"],"end":140511079,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511057,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1484684811","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511060,"source":"dbSNP","strand":1,"feature_type":"variation","end":140511060,"alleles":["T","C"]},{"strand":1,"feature_type":"variation","end":140511065,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511065,"source":"dbSNP","id":"rs1327547921","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1255382370","clinical_significance":[],"start":140511065,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140511067,"alleles":["AAA","AAACAAA"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140511069,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140511069,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795637078"},{"strand":1,"feature_type":"variation","end":140511075,"alleles":["AAA","AAAA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511073,"source":"dbSNP","seq_region_name":"7","id":"rs1196499739","clinical_significance":[]},{"clinical_significance":[],"id":"rs1481646130","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511073,"feature_type":"variation","strand":1,"end":140511090,"alleles":["AAATAAAATAAAATAAAA","AAATAAAATAAAA","AAATAAAATAAAATAAAATAAAA"]},{"clinical_significance":[],"id":"rs1795637152","seq_region_name":"7","alleles":["T","A","C"],"end":140511076,"feature_type":"variation","strand":1,"source":"dbSNP","start":140511076,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["A","T"],"end":140511077,"strand":1,"feature_type":"variation","start":140511077,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs897541592","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1208427909","alleles":["AAAA","AAA"],"end":140511080,"feature_type":"variation","strand":1,"source":"dbSNP","start":140511077,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140511081,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511081,"clinical_significance":[],"id":"rs1795637258","seq_region_name":"7"},{"source":"dbSNP","start":140511087,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140511087,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs996276648"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140511090,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511090,"source":"dbSNP","seq_region_name":"7","id":"rs2130430050","clinical_significance":[]},{"seq_region_name":"7","id":"rs993362238","clinical_significance":[],"strand":1,"feature_type":"variation","end":140511092,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511092,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1033059191","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511101,"feature_type":"variation","strand":1,"end":140511101,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795637381","alleles":["AA","A"],"end":140511105,"feature_type":"variation","strand":1,"source":"dbSNP","start":140511104,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140511105,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511105,"clinical_significance":[],"seq_region_name":"7","id":"rs2130430063"},{"end":140511107,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140511107,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795637409"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1030155981","feature_type":"variation","strand":1,"end":140511118,"alleles":["TTTTTTTTTTTT","TTTTTTTTTT","TTTTTTTTTTT","TTTTTTTTTTTTT","TTTTTTTTTTTTTT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511107},{"start":140511109,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140511108,"alleles":["-","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1196197134","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs954631581","end":140511111,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140511111,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs986470500","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140511114,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511114,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795637582","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511117,"source":"dbSNP","strand":1,"feature_type":"variation","end":140511117,"alleles":["T","C"]},{"id":"rs1398055435","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140511118,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511118,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1472917457","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511119,"feature_type":"variation","strand":1,"end":140511119,"alleles":["G","C","T"]},{"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140511120,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511120,"clinical_significance":[],"seq_region_name":"7","id":"rs1184236146"},{"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140511121,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511121,"clinical_significance":[],"seq_region_name":"7","id":"rs1409586475"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1017490387","end":140511122,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140511122,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1795637766","seq_region_name":"7","alleles":["A","-"],"end":140511122,"feature_type":"variation","strand":1,"source":"dbSNP","start":140511122,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511124,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GG","G"],"end":140511125,"id":"rs1795637792","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs563912527","clinical_significance":[],"strand":1,"feature_type":"variation","end":140511127,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511127,"source":"dbSNP"},{"end":140511132,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140511132,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1166916233"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795637886","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511133,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140511133},{"clinical_significance":[],"id":"rs1472142713","seq_region_name":"7","source":"dbSNP","start":140511135,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140511135,"feature_type":"variation","strand":1},{"id":"rs1795637941","seq_region_name":"7","clinical_significance":[],"end":140511140,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140511140,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1585527283","seq_region_name":"7","clinical_significance":[],"end":140511142,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140511142,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511143,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140511143,"seq_region_name":"7","id":"rs2130430110","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795637983","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140511144,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511144},{"seq_region_name":"7","id":"rs1585527288","clinical_significance":[],"end":140511153,"alleles":["T","C","G"],"strand":1,"feature_type":"variation","start":140511153,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511156,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140511156,"seq_region_name":"7","id":"rs1367869773","clinical_significance":[]},{"id":"rs1585527293","seq_region_name":"7","clinical_significance":[],"start":140511158,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140511158,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140511162,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140511162,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1182466646","seq_region_name":"7"},{"alleles":["C","G","T"],"end":140511163,"feature_type":"variation","strand":1,"source":"dbSNP","start":140511163,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1391751495"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140511164,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511164,"source":"dbSNP","seq_region_name":"7","id":"rs1248513826","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs958287308","source":"dbSNP","start":140511166,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140511166,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs531989037","clinical_significance":[],"alleles":["C","T"],"end":140511169,"strand":1,"feature_type":"variation","start":140511169,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs914013825","source":"dbSNP","start":140511170,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140511170,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795638256","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511171,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140511171},{"clinical_significance":[],"id":"rs945456322","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511172,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140511172},{"seq_region_name":"7","id":"rs1356058727","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511176,"source":"dbSNP","strand":1,"feature_type":"variation","end":140511176,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1795638349","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140511178,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511178,"source":"dbSNP"},{"source":"dbSNP","start":140511181,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140511181,"alleles":["A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs2130430149","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140511182,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511182,"clinical_significance":[],"seq_region_name":"7","id":"rs1795638370"},{"seq_region_name":"7","id":"rs1410452933","clinical_significance":[],"start":140511186,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140511186,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1290760568","source":"dbSNP","start":140511187,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140511187,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511188,"source":"dbSNP","strand":1,"feature_type":"variation","end":140511188,"alleles":["C","G","T"],"seq_region_name":"7","id":"rs1334448759","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140511189,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511189,"source":"dbSNP","seq_region_name":"7","id":"rs1795638511","clinical_significance":[]},{"alleles":["T","G"],"end":140511190,"strand":1,"feature_type":"variation","start":140511190,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1445401200","clinical_significance":[]},{"alleles":["C","T"],"end":140511191,"strand":1,"feature_type":"variation","start":140511191,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1394816715","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795638589","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511192,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140511192},{"seq_region_name":"7","id":"rs1327477292","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140511193,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511193,"source":"dbSNP"},{"alleles":["G","A"],"end":140511194,"feature_type":"variation","strand":1,"source":"dbSNP","start":140511194,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs535997250","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585527324","end":140511196,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140511196,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140511199,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140511199,"alleles":["C","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130430170","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140511200,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511200,"clinical_significance":[],"seq_region_name":"7","id":"rs1228192590"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511201,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140511201,"id":"rs1158862675","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140511205,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511205,"source":"dbSNP","seq_region_name":"7","id":"rs1795638767","clinical_significance":[]},{"source":"dbSNP","start":140511209,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140511209,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1455294060"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140511211,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511211,"clinical_significance":[],"seq_region_name":"7","id":"rs1378389280"},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140511219,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511219,"source":"dbSNP","seq_region_name":"7","id":"rs1795638853","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140511221,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511221,"clinical_significance":[],"id":"rs2130430179","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140511228,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511228,"clinical_significance":[],"seq_region_name":"7","id":"rs1795638873"},{"source":"dbSNP","start":140511231,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140511231,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs982275340","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1285136866","source":"dbSNP","start":140511234,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140511234,"feature_type":"variation","strand":1},{"start":140511235,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140511235,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1358081369","clinical_significance":[]},{"start":140511238,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140511238,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1207698129","clinical_significance":[]},{"start":140511241,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140511241,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1384642925","clinical_significance":[]},{"end":140511245,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140511245,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1483103625","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1288596306","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["CGCACTCCACCACGCC","C"],"end":140511260,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511245,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140511246,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511246,"source":"dbSNP","seq_region_name":"7","id":"rs111955154","clinical_significance":[]},{"start":140511247,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140511247,"strand":1,"feature_type":"variation","id":"rs1249564063","seq_region_name":"7","clinical_significance":[]},{"end":140511248,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","start":140511248,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs77351879","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs888673537","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511250,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","G"],"end":140511250},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511255,"feature_type":"variation","strand":1,"end":140511255,"alleles":["C","T"],"clinical_significance":[],"id":"rs1349246897","seq_region_name":"7"},{"end":140511256,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140511256,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1285894512","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511257,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140511257,"clinical_significance":[],"seq_region_name":"7","id":"rs542286389"},{"alleles":["G","A","T"],"end":140511258,"strand":1,"feature_type":"variation","start":140511258,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795639396","clinical_significance":[]},{"start":140511258,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","GG"],"end":140511258,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795639424","clinical_significance":[]},{"alleles":["C","T"],"end":140511260,"strand":1,"feature_type":"variation","start":140511260,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1473935007","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140511261,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511261,"source":"dbSNP","seq_region_name":"7","id":"rs1161694385","clinical_significance":[]},{"start":140511262,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140511262,"strand":1,"feature_type":"variation","id":"rs1413261799","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs13224083","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511264,"source":"dbSNP","strand":1,"feature_type":"variation","end":140511264,"alleles":["C","A"]},{"start":140511267,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140511267,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1430519994","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511268,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140511268,"id":"rs1309878450","seq_region_name":"7","clinical_significance":[]},{"id":"rs1795639572","seq_region_name":"7","clinical_significance":[],"start":140511268,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140511268,"alleles":["G","-"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140511273,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140511273,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795639599"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795639622","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140511276,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511276},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140511281,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511281,"clinical_significance":[],"seq_region_name":"7","id":"rs1304939698"},{"feature_type":"variation","strand":1,"end":140511282,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511282,"clinical_significance":[],"id":"rs1795639654","seq_region_name":"7"},{"seq_region_name":"7","id":"rs2130430259","clinical_significance":[],"start":140511284,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140511284,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140511290,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140511290,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1369302638"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1330088808","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140511291,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511291},{"clinical_significance":[],"seq_region_name":"7","id":"rs1318789319","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140511292,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511292},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511295,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140511295,"seq_region_name":"7","id":"rs1383700895","clinical_significance":[]},{"id":"rs1358588401","seq_region_name":"7","clinical_significance":[],"alleles":["C","A","T"],"end":140511301,"strand":1,"feature_type":"variation","start":140511301,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs941697806","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140511302,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511302},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795639818","source":"dbSNP","start":140511306,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140511306,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511311,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140511311,"clinical_significance":[],"seq_region_name":"7","id":"rs1795639839"},{"strand":1,"feature_type":"variation","end":140511314,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511314,"source":"dbSNP","id":"rs1795639856","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1335356743","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140511316,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511316},{"seq_region_name":"7","id":"rs1795639897","clinical_significance":[],"end":140511318,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140511318,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140511320,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140511320,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1170839909"},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140511321,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511321,"clinical_significance":[],"seq_region_name":"7","id":"rs1722974800"},{"seq_region_name":"7","id":"rs1795639939","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511322,"source":"dbSNP","strand":1,"feature_type":"variation","end":140511322,"alleles":["G","C"]},{"alleles":["C","A"],"end":140511325,"feature_type":"variation","strand":1,"source":"dbSNP","start":140511325,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1342625108","seq_region_name":"7"},{"source":"dbSNP","start":140511327,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140511327,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585527397"},{"start":140511329,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140511329,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1242913396","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140511334,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511334,"clinical_significance":[],"id":"rs1795640011","seq_region_name":"7"},{"clinical_significance":[],"id":"rs13240511","seq_region_name":"7","feature_type":"variation","strand":1,"end":140511336,"alleles":["G","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511336},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511342,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140511342,"seq_region_name":"7","id":"rs897605276","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511343,"source":"dbSNP","strand":1,"feature_type":"variation","end":140511343,"alleles":["G","A","C"],"seq_region_name":"7","id":"rs1262859745","clinical_significance":[]},{"start":140511345,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140511345,"strand":1,"feature_type":"variation","id":"rs1795640128","seq_region_name":"7","clinical_significance":[]},{"end":140511348,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140511348,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795640154","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1212266824","source":"dbSNP","start":140511349,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140511349,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140511350,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140511350,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795640189","seq_region_name":"7"},{"alleles":["C","T"],"end":140511351,"strand":1,"feature_type":"variation","start":140511351,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1342380846","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511352,"feature_type":"variation","strand":1,"end":140511352,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs531059592"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795640272","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140511354,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511354},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511357,"feature_type":"variation","strand":1,"end":140511357,"alleles":["C","G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1281859640"},{"source":"dbSNP","start":140511360,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140511360,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs780226475"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585527422","feature_type":"variation","strand":1,"end":140511363,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511363},{"source":"dbSNP","start":140511366,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140511366,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs993226324"},{"clinical_significance":[],"seq_region_name":"7","id":"rs145913392","source":"dbSNP","start":140511368,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140511368,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511369,"source":"dbSNP","strand":1,"feature_type":"variation","end":140511369,"alleles":["G","A","C"],"id":"rs1297306269","seq_region_name":"7","clinical_significance":[]},{"id":"rs890306226","seq_region_name":"7","clinical_significance":[],"start":140511374,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140511374,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140511375,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140511375,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1377186476"},{"seq_region_name":"7","id":"rs1332355281","clinical_significance":[],"start":140511378,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140511378,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1341416971","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511379,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140511379},{"clinical_significance":[],"seq_region_name":"7","id":"rs1200957356","end":140511380,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140511380,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511381,"source":"dbSNP","strand":1,"feature_type":"variation","end":140511381,"alleles":["T","G"],"seq_region_name":"7","id":"rs1169894734","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140511386,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511386,"clinical_significance":[],"id":"rs1476941354","seq_region_name":"7"},{"id":"rs1795640649","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140511388,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511388,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795640668","clinical_significance":[],"start":140511389,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140511389,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140511390,"alleles":["G","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511390,"clinical_significance":[],"seq_region_name":"7","id":"rs1795640686"},{"seq_region_name":"7","id":"rs566092557","clinical_significance":[],"start":140511391,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140511391,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140511392,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140511392,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1189024141"},{"id":"rs2130430368","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140511395,"alleles":["CCC","CC"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511393,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs13224211","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511395,"feature_type":"variation","strand":1,"end":140511395,"alleles":["C","T"]},{"id":"rs957978011","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140511396,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511396,"source":"dbSNP"},{"end":140511397,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140511397,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs552102402"},{"source":"dbSNP","start":140511398,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140511398,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1242788526"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795640873","end":140511400,"alleles":["C","A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140511400,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511401,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140511401,"seq_region_name":"7","id":"rs2130430388","clinical_significance":[]},{"end":140511405,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140511405,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130430391","clinical_significance":[]},{"start":140511406,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140511405,"alleles":["-","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795640906","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511406,"source":"dbSNP","strand":1,"feature_type":"variation","end":140511406,"alleles":["C","A","G","T"],"id":"rs570407263","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs149792321","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511407,"feature_type":"variation","strand":1,"end":140511418,"alleles":["TTTTTTTTTTTT","TTTTTTTTTT","TTTTTTTTTTT","TTTTTTTTTTTTT","TTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTT"]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140511410,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511410,"source":"dbSNP","id":"rs1795641129","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795641160","feature_type":"variation","strand":1,"end":140511411,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511411},{"feature_type":"variation","strand":1,"end":140511413,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511413,"clinical_significance":[],"seq_region_name":"7","id":"rs1233673528"},{"feature_type":"variation","strand":1,"end":140511418,"alleles":["T","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511418,"clinical_significance":[],"id":"rs1450304732","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1170613315","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511419,"source":"dbSNP","strand":1,"feature_type":"variation","end":140511419,"alleles":["A","G","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795641292","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140511421,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511421},{"source":"dbSNP","start":140511424,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140511424,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795641324"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585527476","end":140511426,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140511426,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140511428,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140511428,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795641374","clinical_significance":[]},{"clinical_significance":[],"id":"rs1282336230","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140511429,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511429},{"feature_type":"variation","strand":1,"alleles":["CTTCT","CT"],"end":140511436,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511432,"clinical_significance":[],"id":"rs375931493","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795641477","feature_type":"variation","strand":1,"end":140511434,"alleles":["T","C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511434},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795641503","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511439,"feature_type":"variation","strand":1,"end":140511439,"alleles":["T","C"]},{"feature_type":"variation","strand":1,"end":140511441,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511441,"clinical_significance":[],"seq_region_name":"7","id":"rs1795641526"},{"seq_region_name":"7","id":"rs1355220530","clinical_significance":[],"strand":1,"feature_type":"variation","end":140511446,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511446,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795641577","clinical_significance":[],"start":140511448,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140511448,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs982180506","clinical_significance":[],"end":140511452,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140511452,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1464274161","clinical_significance":[],"start":140511453,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140511453,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1166184868","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140511457,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511457},{"start":140511457,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140511457,"alleles":["G","-"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1399818684","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795641704","alleles":["C","T"],"end":140511461,"feature_type":"variation","strand":1,"source":"dbSNP","start":140511461,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1795641726","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511462,"feature_type":"variation","strand":1,"end":140511462,"alleles":["A","G"]},{"start":140511465,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140511465,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585527490","clinical_significance":[]},{"seq_region_name":"7","id":"rs928025447","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C","T"],"end":140511471,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511471,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs957527074","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140511473,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511473},{"clinical_significance":[],"seq_region_name":"7","id":"rs1181810641","source":"dbSNP","start":140511477,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140511477,"alleles":["T","C"],"feature_type":"variation","strand":1},{"id":"rs755440812","seq_region_name":"7","clinical_significance":[],"end":140511483,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140511483,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1585527498","clinical_significance":[],"end":140511484,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140511484,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511487,"source":"dbSNP","strand":1,"feature_type":"variation","end":140511487,"alleles":["A","C"],"seq_region_name":"7","id":"rs1585527500","clinical_significance":[]},{"end":140511488,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140511488,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1394681224"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585527504","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511490,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140511490},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511493,"source":"dbSNP","strand":1,"feature_type":"variation","end":140511493,"alleles":["T","C"],"id":"rs2130430470","seq_region_name":"7","clinical_significance":[]},{"start":140511494,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140511494,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1333862396","clinical_significance":[]},{"id":"rs1795642058","seq_region_name":"7","clinical_significance":[],"start":140511496,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140511496,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511497,"feature_type":"variation","strand":1,"end":140511497,"alleles":["T","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585527509"},{"clinical_significance":[],"seq_region_name":"7","id":"rs989380185","alleles":["C","G","T"],"end":140511499,"feature_type":"variation","strand":1,"source":"dbSNP","start":140511499,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511500,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140511500,"clinical_significance":[],"seq_region_name":"7","id":"rs1456223350"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511502,"feature_type":"variation","strand":1,"end":140511502,"alleles":["G","A"],"clinical_significance":[],"id":"rs1585527514","seq_region_name":"7"},{"id":"rs1795642196","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511508,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140511508},{"feature_type":"variation","strand":1,"end":140511512,"alleles":["T","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511512,"clinical_significance":[],"seq_region_name":"7","id":"rs1256998486"},{"alleles":["T","C"],"end":140511514,"feature_type":"variation","strand":1,"source":"dbSNP","start":140511514,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1365535188"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1323308517","end":140511520,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140511520,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511525,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140511525,"id":"rs10266514","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795642391","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","-"],"end":140511525,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511525,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140511529,"alleles":["TGATT","TGATTGATT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511525,"clinical_significance":[],"seq_region_name":"7","id":"rs1310263442"},{"source":"dbSNP","start":140511526,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140511526,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs556064112"},{"start":140511528,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140511528,"strand":1,"feature_type":"variation","id":"rs1281403685","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130430518","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511532,"feature_type":"variation","strand":1,"end":140511532,"alleles":["C","G"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511534,"source":"dbSNP","strand":1,"feature_type":"variation","end":140511534,"alleles":["G","A"],"id":"rs573422898","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140511537,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511537,"clinical_significance":[],"seq_region_name":"7","id":"rs1585527542"},{"source":"dbSNP","start":140511539,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140511539,"alleles":["T","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1563109218"},{"strand":1,"feature_type":"variation","end":140511543,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511543,"source":"dbSNP","id":"rs182265250","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["GG","G"],"end":140511544,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511543,"clinical_significance":[],"seq_region_name":"7","id":"rs1376490631"},{"alleles":["C","T"],"end":140511545,"feature_type":"variation","strand":1,"source":"dbSNP","start":140511545,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs367558100"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140511546,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511546,"source":"dbSNP","seq_region_name":"7","id":"rs554145544","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs572423567","end":140511549,"alleles":["C","A","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140511549,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1199711793","source":"dbSNP","start":140511550,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140511550,"alleles":["G","A"],"feature_type":"variation","strand":1},{"start":140511551,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140511551,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1268496678","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140511552,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511552,"source":"dbSNP","id":"rs1795642856","seq_region_name":"7","clinical_significance":[]},{"id":"rs1585527562","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511553,"source":"dbSNP","strand":1,"feature_type":"variation","end":140511553,"alleles":["A","C","T"]},{"end":140511554,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140511554,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1401807672"},{"clinical_significance":[],"id":"rs1585527565","seq_region_name":"7","end":140511556,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140511556,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1410798126","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140511558,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511558},{"clinical_significance":[],"seq_region_name":"7","id":"rs1180016790","source":"dbSNP","start":140511563,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140511563,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140511566,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511566,"source":"dbSNP","seq_region_name":"7","id":"rs1051516337","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795643076","seq_region_name":"7","end":140511567,"alleles":["AA","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140511566,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511568,"feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140511568,"clinical_significance":[],"seq_region_name":"7","id":"rs1795643089"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511568,"feature_type":"variation","strand":1,"alleles":["TTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTT","TTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTT"],"end":140511586,"clinical_significance":[],"seq_region_name":"7","id":"rs61020778"},{"source":"dbSNP","start":140511569,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140511569,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1317515238","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511576,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140511576,"clinical_significance":[],"seq_region_name":"7","id":"rs1585527581"},{"seq_region_name":"7","id":"rs1224165510","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511577,"source":"dbSNP","strand":1,"feature_type":"variation","end":140511577,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1238122024","clinical_significance":[],"end":140511581,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140511581,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1353100489","source":"dbSNP","start":140511583,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140511583,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1585527587","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511586,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140511586},{"strand":1,"feature_type":"variation","alleles":["TG","-"],"end":140511587,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511586,"source":"dbSNP","seq_region_name":"7","id":"rs1304200885","clinical_significance":[]},{"seq_region_name":"7","id":"rs1190743090","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511587,"source":"dbSNP","strand":1,"feature_type":"variation","end":140511587,"alleles":["G","-"]},{"clinical_significance":[],"id":"rs1246359676","seq_region_name":"7","source":"dbSNP","start":140511587,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140511587,"alleles":["G","T"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511591,"source":"dbSNP","strand":1,"feature_type":"variation","end":140511591,"alleles":["C","T"],"id":"rs1795643570","seq_region_name":"7","clinical_significance":[]},{"start":140511592,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140511592,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585527593","clinical_significance":[]},{"start":140511594,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140511594,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585527595","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511595,"source":"dbSNP","strand":1,"feature_type":"variation","end":140511595,"alleles":["G","A"],"seq_region_name":"7","id":"rs1293380851","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511595,"source":"dbSNP","strand":1,"feature_type":"variation","end":140511595,"alleles":["G","-"],"seq_region_name":"7","id":"rs1795643668","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511599,"feature_type":"variation","strand":1,"end":140511599,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1427996573"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511601,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140511601,"clinical_significance":[],"seq_region_name":"7","id":"rs1795643734"},{"seq_region_name":"7","id":"rs1347520157","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511602,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140511602},{"source":"dbSNP","start":140511605,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140511605,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs890170079"},{"seq_region_name":"7","id":"rs1795643819","clinical_significance":[],"start":140511608,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140511608,"alleles":["G","-"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130430620","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511610,"feature_type":"variation","strand":1,"end":140511610,"alleles":["T","C"]},{"id":"rs2130430625","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511611,"source":"dbSNP","strand":1,"feature_type":"variation","end":140511611,"alleles":["T","C"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511612,"source":"dbSNP","strand":1,"feature_type":"variation","end":140511612,"alleles":["A","C"],"seq_region_name":"7","id":"rs1795643840","clinical_significance":[]},{"end":140511616,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140511616,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1007845018"},{"id":"rs1379159969","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140511621,"strand":1,"feature_type":"variation","start":140511621,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511623,"source":"dbSNP","strand":1,"feature_type":"variation","end":140511623,"alleles":["C","A","T"],"id":"rs1585527610","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1199619243","alleles":["G","A","C"],"end":140511624,"feature_type":"variation","strand":1,"source":"dbSNP","start":140511624,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140511626,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140511626,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs2130430639","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","G"],"end":140511629,"feature_type":"variation","strand":1,"source":"dbSNP","start":140511629,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1434604544"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795644010","source":"dbSNP","start":140511630,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140511630,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795644144","feature_type":"variation","strand":1,"end":140511633,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511633},{"alleles":["C","A","T"],"end":140511637,"strand":1,"feature_type":"variation","start":140511637,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1038859138","clinical_significance":[]},{"clinical_significance":[],"id":"rs185449980","seq_region_name":"7","end":140511638,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140511638,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["A","G"],"end":140511643,"feature_type":"variation","strand":1,"source":"dbSNP","start":140511643,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1486059093"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511646,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140511646,"clinical_significance":[],"seq_region_name":"7","id":"rs540900509"},{"seq_region_name":"7","id":"rs1795644300","clinical_significance":[],"strand":1,"feature_type":"variation","end":140511647,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511647,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140511648,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511648,"source":"dbSNP","seq_region_name":"7","id":"rs558526229","clinical_significance":[]},{"alleles":["A","C"],"end":140511649,"strand":1,"feature_type":"variation","start":140511649,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585527631","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511650,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140511650,"clinical_significance":[],"seq_region_name":"7","id":"rs1214396394"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511651,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140511651,"id":"rs1795644427","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795644452","seq_region_name":"7","end":140511655,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140511655,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511660,"feature_type":"variation","strand":1,"end":140511660,"alleles":["C","G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585527637"},{"end":140511661,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140511661,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1352805685","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs576790322","end":140511662,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140511662,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1458539889","seq_region_name":"7","alleles":["G","C"],"end":140511664,"feature_type":"variation","strand":1,"source":"dbSNP","start":140511664,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511665,"feature_type":"variation","strand":1,"end":140511665,"alleles":["T","G"],"clinical_significance":[],"id":"rs1585527643","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585527649","source":"dbSNP","start":140511667,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140511667,"alleles":["T","C"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140511670,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511670,"clinical_significance":[],"seq_region_name":"7","id":"rs1235494496"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1318139925","source":"dbSNP","start":140511676,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140511676,"feature_type":"variation","strand":1},{"alleles":["G","T"],"end":140511681,"strand":1,"feature_type":"variation","start":140511681,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1020805352","seq_region_name":"7","clinical_significance":[]},{"id":"rs1215340023","seq_region_name":"7","clinical_significance":[],"start":140511683,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140511683,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"id":"rs1363962149","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511691,"source":"dbSNP","strand":1,"feature_type":"variation","end":140511691,"alleles":["C","A"]},{"source":"dbSNP","start":140511695,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140511695,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795644857"},{"end":140511701,"alleles":["T","TGAGT"],"strand":1,"feature_type":"variation","start":140511701,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795644882","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511702,"feature_type":"variation","strand":1,"end":140511702,"alleles":["A","C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795644910"},{"source":"dbSNP","start":140511706,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140511706,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs972043673","seq_region_name":"7"},{"start":140511710,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140511710,"alleles":["A","-"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795644948","clinical_significance":[]},{"end":140511712,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140511712,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs966696514"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1386866479","feature_type":"variation","strand":1,"end":140511713,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511713},{"strand":1,"feature_type":"variation","end":140511719,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511719,"source":"dbSNP","seq_region_name":"7","id":"rs1795645040","clinical_significance":[]},{"end":140511723,"alleles":["CC","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140511722,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1399948570"},{"clinical_significance":[],"seq_region_name":"7","id":"rs981153842","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511723,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140511723},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511725,"feature_type":"variation","strand":1,"end":140511725,"alleles":["C","A","G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs565076279"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140511726,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511726,"clinical_significance":[],"seq_region_name":"7","id":"rs936978531"},{"start":140511727,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140511727,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1428698790","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511728,"feature_type":"variation","strand":1,"end":140511728,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1425506506"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1191163883","alleles":["G","T"],"end":140511729,"feature_type":"variation","strand":1,"source":"dbSNP","start":140511729,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1487953399","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511733,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140511733},{"seq_region_name":"7","id":"rs1563109278","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140511735,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511735,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140511736,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511736,"source":"dbSNP","seq_region_name":"7","id":"rs959484548","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1288816186","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140511742,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511742},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795645332","end":140511744,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140511744,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs991421895","clinical_significance":[],"start":140511747,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140511747,"alleles":["T","C","G"],"strand":1,"feature_type":"variation"},{"end":140511748,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140511748,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795645410"},{"seq_region_name":"7","id":"rs973797791","clinical_significance":[],"alleles":["C","T"],"end":140511751,"strand":1,"feature_type":"variation","start":140511751,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511753,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140511753,"clinical_significance":[],"id":"rs1795645463","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1320197863","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511754,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140511754},{"clinical_significance":[],"id":"rs1276767651","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511757,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140511757},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511758,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C","T"],"end":140511758,"seq_region_name":"7","id":"rs36072874","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1266503092","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140511759,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511759},{"source":"dbSNP","start":140511760,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140511760,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795645670"},{"feature_type":"variation","strand":1,"end":140511761,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511761,"clinical_significance":[],"seq_region_name":"7","id":"rs1315407212"},{"clinical_significance":[],"id":"rs1795645699","seq_region_name":"7","source":"dbSNP","start":140511762,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140511762,"feature_type":"variation","strand":1},{"id":"rs1795645719","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511763,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140511763},{"clinical_significance":[],"seq_region_name":"7","id":"rs1394750706","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511765,"feature_type":"variation","strand":1,"end":140511765,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs199781476","feature_type":"variation","strand":1,"alleles":["A","T"],"end":140511766,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511766},{"clinical_significance":[],"seq_region_name":"7","id":"rs541515758","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511767,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140511767},{"source":"dbSNP","start":140511768,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140511768,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs910031161"},{"source":"dbSNP","start":140511770,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140511770,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795645869"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511771,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140511771,"seq_region_name":"7","id":"rs182857658","clinical_significance":[]},{"clinical_significance":[],"id":"rs1585527701","seq_region_name":"7","source":"dbSNP","start":140511774,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140511774,"feature_type":"variation","strand":1},{"end":140511777,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140511777,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs912506823","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs200733639","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140511779,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511779,"source":"dbSNP"},{"seq_region_name":"7","id":"rs527329952","clinical_significance":[],"alleles":["G","T"],"end":140511780,"strand":1,"feature_type":"variation","start":140511780,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795646259","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511781,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140511781},{"source":"dbSNP","start":140511782,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140511782,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs943974324","seq_region_name":"7"},{"source":"dbSNP","start":140511788,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140511788,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795646323"},{"end":140511789,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140511789,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1039614005","clinical_significance":[]},{"alleles":["C","T"],"end":140511792,"strand":1,"feature_type":"variation","start":140511792,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs551741272","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140511798,"alleles":["A","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511798,"clinical_significance":[],"id":"rs1255576925","seq_region_name":"7"},{"start":140511799,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140511799,"alleles":["C","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795646396","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795646423","feature_type":"variation","strand":1,"end":140511803,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511803},{"clinical_significance":[],"id":"rs1795646445","seq_region_name":"7","source":"dbSNP","start":140511805,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140511805,"alleles":["G","A"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140511809,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511809,"clinical_significance":[],"seq_region_name":"7","id":"rs150806151"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511810,"source":"dbSNP","strand":1,"feature_type":"variation","end":140511810,"alleles":["G","A","T"],"seq_region_name":"7","id":"rs1459313241","clinical_significance":[]},{"id":"rs1256360898","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511815,"source":"dbSNP","strand":1,"feature_type":"variation","end":140511815,"alleles":["C","T"]},{"end":140511818,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140511818,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1198467177"},{"end":140511819,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140511819,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1473794740"},{"clinical_significance":[],"id":"rs1267563937","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511821,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140511821},{"start":140511824,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140511824,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795646604","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795646622","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140511832,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511832},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140511842,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511842,"clinical_significance":[],"id":"rs183477706","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1795646672","seq_region_name":"7","alleles":["G","A"],"end":140511844,"feature_type":"variation","strand":1,"source":"dbSNP","start":140511844,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1054582038","clinical_significance":[],"end":140511849,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140511849,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs893200670","feature_type":"variation","strand":1,"end":140511851,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511851},{"seq_region_name":"7","id":"rs1010432851","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140511857,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511857,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511858,"feature_type":"variation","strand":1,"end":140511858,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1344291425"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511859,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140511859,"clinical_significance":[],"seq_region_name":"7","id":"rs1795646771"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511860,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140511860,"seq_region_name":"7","id":"rs1311458478","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795646800","clinical_significance":[],"start":140511864,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140511864,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1795646828","clinical_significance":[],"start":140511874,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140511874,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140511875,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511875,"clinical_significance":[],"id":"rs1795646839","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511878,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140511878,"seq_region_name":"7","id":"rs531480650","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511883,"feature_type":"variation","strand":1,"end":140511883,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1446875938"},{"seq_region_name":"7","id":"rs2130430854","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140511886,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511886,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511887,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140511887,"seq_region_name":"7","id":"rs911678479","clinical_significance":[]},{"start":140511888,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140511888,"alleles":["G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1328904633","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795646945","alleles":["T","C"],"end":140511890,"feature_type":"variation","strand":1,"source":"dbSNP","start":140511890,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["A","G"],"end":140511894,"strand":1,"feature_type":"variation","start":140511894,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1020853290","clinical_significance":[]},{"end":140511894,"alleles":["A","AA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140511894,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795646983","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1795646998","seq_region_name":"7","alleles":["T","C"],"end":140511903,"feature_type":"variation","strand":1,"source":"dbSNP","start":140511903,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1795647026","seq_region_name":"7","clinical_significance":[],"alleles":["G","C"],"end":140511904,"strand":1,"feature_type":"variation","start":140511904,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795647045","clinical_significance":[],"alleles":["G","A"],"end":140511908,"strand":1,"feature_type":"variation","start":140511908,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1795647063","seq_region_name":"7","clinical_significance":[],"start":140511915,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140511915,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1563109342","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511916,"source":"dbSNP","strand":1,"feature_type":"variation","end":140511916,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs943120886","clinical_significance":[],"start":140511917,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140511917,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140511921,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511921,"source":"dbSNP","id":"rs1391198416","seq_region_name":"7","clinical_significance":[]},{"end":140511922,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140511922,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs971565501","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795647173","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511924,"feature_type":"variation","strand":1,"end":140511924,"alleles":["A","G"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511930,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140511930,"clinical_significance":[],"id":"rs1795647193","seq_region_name":"7"},{"id":"rs1795647209","seq_region_name":"7","clinical_significance":[],"start":140511935,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140511935,"strand":1,"feature_type":"variation"},{"end":140511939,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140511939,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795647231","seq_region_name":"7"},{"start":140511940,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140511940,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795647241","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140511944,"alleles":["ATCT","ATCTATCT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511941,"source":"dbSNP","id":"rs1795647254","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795647268","source":"dbSNP","start":140511942,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140511944,"alleles":["TCT","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs549965173","seq_region_name":"7","source":"dbSNP","start":140511945,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140511945,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1387938122","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511949,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140511949},{"id":"rs112295727","seq_region_name":"7","clinical_significance":[],"start":140511951,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140511951,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs958405516","clinical_significance":[],"alleles":["C","T"],"end":140511956,"strand":1,"feature_type":"variation","start":140511956,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140511959,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140511959,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795647335"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511961,"feature_type":"variation","strand":1,"end":140511961,"alleles":["C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795647354"},{"start":140511965,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140511965,"alleles":["A","G"],"strand":1,"feature_type":"variation","id":"rs2130430917","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs574086170","end":140511968,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140511968,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795647397","alleles":["T","C"],"end":140511969,"feature_type":"variation","strand":1,"source":"dbSNP","start":140511969,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795647415","clinical_significance":[],"alleles":["G","A"],"end":140511971,"strand":1,"feature_type":"variation","start":140511971,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1441594450","clinical_significance":[],"start":140511975,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140511975,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1795647453","clinical_significance":[],"end":140511979,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140511979,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs188296889","clinical_significance":[],"end":140511981,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140511981,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1178291912","clinical_significance":[],"end":140511982,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140511982,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140511984,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140511984,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795647492"},{"seq_region_name":"7","id":"rs1042294189","clinical_significance":[],"start":140511987,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140511987,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1795647544","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140511987,"source":"dbSNP","strand":1,"feature_type":"variation","end":140511988,"alleles":["CC","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795647568","feature_type":"variation","strand":1,"end":140511988,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140511988},{"start":140511989,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140511989,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs951189212","clinical_significance":[]},{"seq_region_name":"7","id":"rs1208414457","clinical_significance":[],"alleles":["T","TT"],"end":140511991,"strand":1,"feature_type":"variation","start":140511991,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["T","G"],"end":140511991,"strand":1,"feature_type":"variation","start":140511991,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795647608","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs982531397","end":140511992,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140511992,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140511993,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140511993,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795647661","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1356340669","source":"dbSNP","start":140511995,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140511995,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795647702","clinical_significance":[],"strand":1,"feature_type":"variation","end":140512000,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512000,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512001,"feature_type":"variation","strand":1,"end":140512001,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795647721"},{"seq_region_name":"7","id":"rs563000673","clinical_significance":[],"start":140512002,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TTTTTTTTT","TTTTTTTT","TTTTTTTTTT"],"end":140512010,"strand":1,"feature_type":"variation"},{"start":140512010,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A","C"],"end":140512010,"strand":1,"feature_type":"variation","id":"rs1795647774","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795647789","source":"dbSNP","start":140512012,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140512012,"alleles":["G","T"],"feature_type":"variation","strand":1},{"alleles":["C","T"],"end":140512014,"strand":1,"feature_type":"variation","start":140512014,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795647815","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1355270246","feature_type":"variation","strand":1,"end":140512017,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512017},{"feature_type":"variation","strand":1,"end":140512018,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512018,"clinical_significance":[],"seq_region_name":"7","id":"rs1563109365"},{"alleles":["TGTTGTT","TGTT"],"end":140512025,"feature_type":"variation","strand":1,"source":"dbSNP","start":140512019,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs902401590"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1445603694","feature_type":"variation","strand":1,"alleles":["G","-"],"end":140512023,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512023},{"feature_type":"variation","strand":1,"end":140512023,"alleles":["-","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512024,"clinical_significance":[],"seq_region_name":"7","id":"rs1331312450"},{"seq_region_name":"7","id":"rs1795647961","clinical_significance":[],"start":140512024,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140512030,"alleles":["TTTTTTT","TTTTTT"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1795647977","clinical_significance":[],"alleles":["T","C"],"end":140512027,"strand":1,"feature_type":"variation","start":140512027,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1325360113","seq_region_name":"7","alleles":["T","G"],"end":140512028,"feature_type":"variation","strand":1,"source":"dbSNP","start":140512028,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1795648007","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140512030,"strand":1,"feature_type":"variation","start":140512030,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585527772","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140512034,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512034},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140512035,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512035,"source":"dbSNP","id":"rs1384835713","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1287461305","clinical_significance":[],"strand":1,"feature_type":"variation","end":140512041,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512041,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512046,"source":"dbSNP","strand":1,"feature_type":"variation","end":140512046,"alleles":["G","A"],"seq_region_name":"7","id":"rs1795648106","clinical_significance":[]},{"seq_region_name":"7","id":"rs866559488","clinical_significance":[],"strand":1,"feature_type":"variation","end":140512050,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512050,"source":"dbSNP"},{"seq_region_name":"7","id":"rs912398631","clinical_significance":[],"strand":1,"feature_type":"variation","end":140512056,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512056,"source":"dbSNP"},{"seq_region_name":"7","id":"rs10270200","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512057,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140512057},{"source":"dbSNP","start":140512062,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140512062,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795648286"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1034978701","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140512063,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512063},{"seq_region_name":"7","id":"rs1378553729","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140512064,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512064,"source":"dbSNP"},{"alleles":["A","T"],"end":140512065,"strand":1,"feature_type":"variation","start":140512065,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795648370","clinical_significance":[]},{"id":"rs959741940","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512070,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140512070},{"source":"dbSNP","start":140512071,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140512071,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1379582017"},{"feature_type":"variation","strand":1,"alleles":["T","-"],"end":140512072,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512072,"clinical_significance":[],"seq_region_name":"7","id":"rs1267364340"},{"clinical_significance":[],"id":"rs1585527797","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140512073,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512073},{"clinical_significance":[],"seq_region_name":"7","id":"rs116237908","end":140512074,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140512074,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1795648591","seq_region_name":"7","clinical_significance":[],"alleles":["G","T"],"end":140512078,"strand":1,"feature_type":"variation","start":140512078,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1221756345","clinical_significance":[],"start":140512080,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140512080,"strand":1,"feature_type":"variation"},{"end":140512083,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140512083,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs921178704","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512084,"source":"dbSNP","strand":1,"feature_type":"variation","end":140512084,"alleles":["C","A"],"seq_region_name":"7","id":"rs1795648674","clinical_significance":[]},{"seq_region_name":"7","id":"rs1017403885","clinical_significance":[],"start":140512087,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140512087,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1264303094","clinical_significance":[],"strand":1,"feature_type":"variation","end":140512090,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512090,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140512100,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512100,"source":"dbSNP","seq_region_name":"7","id":"rs1795648756","clinical_significance":[]},{"source":"dbSNP","start":140512101,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140512101,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs932002087","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795648811","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512102,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140512102},{"seq_region_name":"7","id":"rs1054444894","clinical_significance":[],"strand":1,"feature_type":"variation","end":140512103,"alleles":["T","A","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512103,"source":"dbSNP"},{"id":"rs893244103","seq_region_name":"7","clinical_significance":[],"end":140512104,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140512104,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1180522876","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512105,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140512105},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512107,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140512107,"seq_region_name":"7","id":"rs1407714084","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795648937","clinical_significance":[],"end":140512110,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140512110,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140512114,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512114,"clinical_significance":[],"seq_region_name":"7","id":"rs1345331257"},{"end":140512115,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140512115,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1010754873"},{"seq_region_name":"7","id":"rs757086296","clinical_significance":[],"strand":1,"feature_type":"variation","end":140512116,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512116,"source":"dbSNP"},{"seq_region_name":"7","id":"rs564293602","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512122,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140512122},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512123,"source":"dbSNP","strand":1,"feature_type":"variation","end":140512123,"alleles":["G","A"],"id":"rs1423482758","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512126,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140512126,"clinical_significance":[],"seq_region_name":"7","id":"rs539873174"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512127,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140512127,"seq_region_name":"7","id":"rs987164083","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140512129,"alleles":["T","A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512129,"source":"dbSNP","seq_region_name":"7","id":"rs1002994533","clinical_significance":[]},{"alleles":["T","C","G"],"end":140512131,"strand":1,"feature_type":"variation","start":140512131,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795649105","clinical_significance":[]},{"seq_region_name":"7","id":"rs911543685","clinical_significance":[],"strand":1,"feature_type":"variation","end":140512142,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512142,"source":"dbSNP"},{"alleles":["G","T"],"end":140512152,"feature_type":"variation","strand":1,"source":"dbSNP","start":140512152,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795649200"},{"end":140512159,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140512159,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs558159966","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140512164,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512164,"clinical_significance":[],"id":"rs1415075901","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1315115940","source":"dbSNP","start":140512167,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140512167,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs943006772","end":140512168,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140512168,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1477785533","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512169,"feature_type":"variation","strand":1,"end":140512169,"alleles":["A","-"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512169,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140512169,"id":"rs2130431105","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs778638063","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512170,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140512170},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795649415","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512171,"feature_type":"variation","strand":1,"end":140512171,"alleles":["G","A"]},{"start":140512172,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140512172,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs576693320","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140512174,"alleles":["A","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512174,"clinical_significance":[],"seq_region_name":"7","id":"rs1196287778"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1263063295","feature_type":"variation","strand":1,"alleles":["C","A","G","T"],"end":140512175,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512175},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140512181,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512181,"source":"dbSNP","seq_region_name":"7","id":"rs1245400763","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140512186,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512186,"clinical_significance":[],"id":"rs1741463106","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1214519456","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512191,"feature_type":"variation","strand":1,"end":140512191,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs914942766","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512192,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140512192},{"seq_region_name":"7","id":"rs1280077357","clinical_significance":[],"alleles":["G","A"],"end":140512193,"strand":1,"feature_type":"variation","start":140512193,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["C","A"],"end":140512195,"feature_type":"variation","strand":1,"source":"dbSNP","start":140512195,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs537310237","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs74778059","alleles":["C","A","T"],"end":140512197,"feature_type":"variation","strand":1,"source":"dbSNP","start":140512197,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1027087260","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512201,"source":"dbSNP","strand":1,"feature_type":"variation","end":140512201,"alleles":["T","C"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512206,"source":"dbSNP","strand":1,"feature_type":"variation","end":140512206,"alleles":["C","A","G","T"],"seq_region_name":"7","id":"rs902475355","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795649897","seq_region_name":"7","alleles":["C","T"],"end":140512207,"feature_type":"variation","strand":1,"source":"dbSNP","start":140512207,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["-","GA"],"end":140512209,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512210,"clinical_significance":[],"seq_region_name":"7","id":"rs1448620937"},{"clinical_significance":[],"seq_region_name":"7","id":"rs951054165","feature_type":"variation","strand":1,"end":140512210,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512210},{"seq_region_name":"7","id":"rs1795649973","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512211,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140512211},{"seq_region_name":"7","id":"rs1795649999","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512214,"source":"dbSNP","strand":1,"feature_type":"variation","end":140512214,"alleles":["C","T"]},{"strand":1,"feature_type":"variation","alleles":["C","A","G","T"],"end":140512216,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512216,"source":"dbSNP","id":"rs528401141","seq_region_name":"7","clinical_significance":[]},{"end":140512216,"alleles":["-","AGAG"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140512217,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs141510456","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140512217,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512217,"clinical_significance":[],"seq_region_name":"7","id":"rs372894386"},{"seq_region_name":"7","id":"rs549140968","clinical_significance":[],"strand":1,"feature_type":"variation","end":140512219,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512219,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140512220,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512220,"source":"dbSNP","seq_region_name":"7","id":"rs2130431179","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512223,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140512223,"clinical_significance":[],"seq_region_name":"7","id":"rs1483788324"},{"clinical_significance":[],"id":"rs895159852","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512224,"feature_type":"variation","strand":1,"end":140512224,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1012625653","clinical_significance":[],"alleles":["C","T"],"end":140512226,"strand":1,"feature_type":"variation","start":140512226,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1183927565","clinical_significance":[],"end":140512228,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140512228,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140512231,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140512231,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795650294"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1474020962","feature_type":"variation","strand":1,"end":140512233,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512233},{"clinical_significance":[],"id":"rs1795650342","seq_region_name":"7","source":"dbSNP","start":140512236,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140512236,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1238715389","alleles":["T","C"],"end":140512240,"feature_type":"variation","strand":1,"source":"dbSNP","start":140512240,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs912272253","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512242,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140512242},{"clinical_significance":[],"seq_region_name":"7","id":"rs1721579948","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140512245,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512245},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140512246,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512246,"clinical_significance":[],"seq_region_name":"7","id":"rs1795650420"},{"seq_region_name":"7","id":"rs1795650454","clinical_significance":[],"start":140512248,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140512248,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1460645349","clinical_significance":[],"alleles":["C","G"],"end":140512250,"strand":1,"feature_type":"variation","start":140512250,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs61003189","feature_type":"variation","strand":1,"end":140512252,"alleles":["G","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512252},{"start":140512252,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140512252,"alleles":["G","T"],"strand":1,"feature_type":"variation","id":"rs1680456759","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1200355233","source":"dbSNP","start":140512256,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140512256,"feature_type":"variation","strand":1},{"start":140512262,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140512262,"strand":1,"feature_type":"variation","id":"rs1168718645","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs898572035","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512263,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140512263},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512270,"feature_type":"variation","strand":1,"end":140512270,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795650604"},{"feature_type":"variation","strand":1,"end":140512273,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512273,"clinical_significance":[],"seq_region_name":"7","id":"rs2130431221"},{"end":140512280,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140512280,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1228836083","seq_region_name":"7","clinical_significance":[]},{"start":140512286,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TTT","TTTT"],"end":140512288,"strand":1,"feature_type":"variation","id":"rs1391475918","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140512288,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["-","A"],"end":140512287,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1282571929"},{"seq_region_name":"7","id":"rs994371131","clinical_significance":[],"end":140512288,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140512288,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140512289,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140512289,"alleles":["A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795650955","clinical_significance":[]},{"id":"rs201869968","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512289,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AAAAAAAA","AAAAAAA","AAAAAAAAA"],"end":140512296},{"end":140512293,"alleles":["-","C"],"strand":1,"feature_type":"variation","start":140512294,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1464226222","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs546060259","feature_type":"variation","strand":1,"alleles":["-","T"],"end":140512295,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512296},{"alleles":["A","T"],"end":140512296,"strand":1,"feature_type":"variation","start":140512296,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs76928327","clinical_significance":[]},{"seq_region_name":"7","id":"rs542034776","clinical_significance":[],"alleles":["-","AT","C"],"end":140512296,"strand":1,"feature_type":"variation","start":140512297,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs571786623","seq_region_name":"7","clinical_significance":[],"start":140512297,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140512297,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs35043631","end":140512305,"alleles":["TTTTTTTTT","TTTTTTTT","TTTTTTTTTT","TTTTTTTTTTT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140512297,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1795651320","seq_region_name":"7","clinical_significance":[],"end":140512327,"alleles":["TTTAACTTTTTTTGTTGTTTTGTTT","TTT"],"strand":1,"feature_type":"variation","start":140512303,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["T","A"],"end":140512305,"feature_type":"variation","strand":1,"source":"dbSNP","start":140512305,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1456132046"},{"strand":1,"feature_type":"variation","end":140512306,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512306,"source":"dbSNP","seq_region_name":"7","id":"rs1359603510","clinical_significance":[]},{"clinical_significance":[],"id":"rs397753813","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512306,"feature_type":"variation","strand":1,"end":140512307,"alleles":["AA","AAA"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512309,"feature_type":"variation","strand":1,"end":140512315,"alleles":["TTTTTTT","TTTTTT"],"clinical_significance":[],"seq_region_name":"7","id":"rs1323476013"},{"alleles":["T","C"],"end":140512313,"feature_type":"variation","strand":1,"source":"dbSNP","start":140512313,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1449991456","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1018914990","source":"dbSNP","start":140512316,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140512316,"alleles":["G","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795651580","clinical_significance":[],"alleles":["T","C"],"end":140512318,"strand":1,"feature_type":"variation","start":140512318,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140512319,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","-"],"end":140512319,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1354542963","clinical_significance":[]},{"id":"rs1795651608","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140512319,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512319,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1300843415","feature_type":"variation","strand":1,"end":140512320,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512320},{"alleles":["T","C"],"end":140512322,"feature_type":"variation","strand":1,"source":"dbSNP","start":140512322,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795651668"},{"id":"rs2130431300","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140512323,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512323,"source":"dbSNP"},{"alleles":["G","C"],"end":140512324,"strand":1,"feature_type":"variation","start":140512324,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795651688","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795651700","source":"dbSNP","start":140512329,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140512329,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140512336,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512336,"clinical_significance":[],"id":"rs1795651735","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1311466522","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140512338,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512338},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512342,"source":"dbSNP","strand":1,"feature_type":"variation","end":140512342,"alleles":["G","-"],"id":"rs139196888","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140512342,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512342,"source":"dbSNP","seq_region_name":"7","id":"rs1376418313","clinical_significance":[]},{"end":140512344,"alleles":["TT","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140512343,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795651833"},{"start":140512344,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140512344,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1294549786","clinical_significance":[]},{"seq_region_name":"7","id":"rs192807576","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512347,"source":"dbSNP","strand":1,"feature_type":"variation","end":140512347,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs183049833","clinical_significance":[],"alleles":["C","T"],"end":140512348,"strand":1,"feature_type":"variation","start":140512348,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795651998","clinical_significance":[],"alleles":["G","T"],"end":140512350,"strand":1,"feature_type":"variation","start":140512350,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs921208512","clinical_significance":[],"end":140512352,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140512352,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140512354,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140512354,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs974776651","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795652069","clinical_significance":[],"strand":1,"feature_type":"variation","end":140512358,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512358,"source":"dbSNP"},{"source":"dbSNP","start":140512359,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140512359,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1348695841","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs149552794","source":"dbSNP","start":140512361,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140512361,"alleles":["A","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1795652124","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512363,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140512363},{"start":140512369,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140512369,"alleles":["A","G"],"strand":1,"feature_type":"variation","id":"rs1795652139","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140512374,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140512374,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795652162"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140512376,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512376,"clinical_significance":[],"seq_region_name":"7","id":"rs1298500685"},{"seq_region_name":"7","id":"rs1420796033","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512383,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140512383},{"clinical_significance":[],"seq_region_name":"7","id":"rs1367460076","alleles":["T","G"],"end":140512395,"feature_type":"variation","strand":1,"source":"dbSNP","start":140512395,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140512398,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["GGG","GG"],"end":140512400,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585528023"},{"alleles":["TCCTCCTC","TCCTC"],"end":140512411,"strand":1,"feature_type":"variation","start":140512404,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795652256","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140512407,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512407,"clinical_significance":[],"seq_region_name":"7","id":"rs1795652267"},{"seq_region_name":"7","id":"rs1795652284","clinical_significance":[],"start":140512409,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140512409,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1795652306","clinical_significance":[],"start":140512412,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AA","AAA"],"end":140512413,"strand":1,"feature_type":"variation"},{"end":140512418,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140512418,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1159918934"},{"seq_region_name":"7","id":"rs1563109458","clinical_significance":[],"end":140512421,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140512421,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140512424,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140512424,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs1437509771","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130431366","source":"dbSNP","start":140512428,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140512428,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795652385","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512432,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140512432},{"clinical_significance":[],"seq_region_name":"7","id":"rs1406750347","end":140512438,"alleles":["TAGCT","TAGCTAGCT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140512434,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140512437,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140512437,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585528031"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512439,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140512439,"clinical_significance":[],"id":"rs1191612120","seq_region_name":"7"},{"alleles":["T","C"],"end":140512446,"strand":1,"feature_type":"variation","start":140512446,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795652438","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512447,"feature_type":"variation","strand":1,"end":140512447,"alleles":["C","G"],"clinical_significance":[],"id":"rs1795652455","seq_region_name":"7"},{"id":"rs1489355651","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512452,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140512452},{"strand":1,"feature_type":"variation","end":140512462,"alleles":["G","C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512462,"source":"dbSNP","seq_region_name":"7","id":"rs1795652498","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140512463,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512463,"source":"dbSNP","seq_region_name":"7","id":"rs1795652524","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795652542","source":"dbSNP","start":140512474,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140512476,"alleles":["GGG","-"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1244728424","clinical_significance":[],"alleles":["GGGCAGG","G"],"end":140512480,"strand":1,"feature_type":"variation","start":140512474,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["C","T"],"end":140512477,"feature_type":"variation","strand":1,"source":"dbSNP","start":140512477,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1221664534","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1795652598","seq_region_name":"7","end":140512480,"alleles":["AGG","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140512478,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["G","A"],"end":140512479,"feature_type":"variation","strand":1,"source":"dbSNP","start":140512479,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795652619"},{"seq_region_name":"7","id":"rs563705439","clinical_significance":[],"start":140512480,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140512480,"alleles":["G","A","C"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140512483,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140512483,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs977926326","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512484,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140512484,"clinical_significance":[],"seq_region_name":"7","id":"rs757964701"},{"source":"dbSNP","start":140512488,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140512488,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1272967696","seq_region_name":"7"},{"start":140512491,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A","C"],"end":140512491,"strand":1,"feature_type":"variation","id":"rs914568818","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs939156908","clinical_significance":[],"start":140512493,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140512493,"alleles":["T","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1795652757","clinical_significance":[],"end":140512497,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140512497,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1056391241","clinical_significance":[],"strand":1,"feature_type":"variation","end":140512499,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512499,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512502,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140512502,"clinical_significance":[],"seq_region_name":"7","id":"rs1313245101"},{"id":"rs1795652827","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512506,"source":"dbSNP","strand":1,"feature_type":"variation","end":140512506,"alleles":["C","G"]},{"strand":1,"feature_type":"variation","end":140512507,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512507,"source":"dbSNP","seq_region_name":"7","id":"rs2130431410","clinical_significance":[]},{"seq_region_name":"7","id":"rs946034188","clinical_significance":[],"strand":1,"feature_type":"variation","end":140512509,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512509,"source":"dbSNP"},{"start":140512516,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140512516,"alleles":["A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795652870","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512518,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140512518,"seq_region_name":"7","id":"rs1795652897","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512519,"source":"dbSNP","strand":1,"feature_type":"variation","end":140512519,"alleles":["C","T"],"seq_region_name":"7","id":"rs1795652916","clinical_significance":[]},{"alleles":["A","C","G"],"end":140512520,"strand":1,"feature_type":"variation","start":140512520,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130431420","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130431426","alleles":["C","T"],"end":140512524,"feature_type":"variation","strand":1,"source":"dbSNP","start":140512524,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs2130431428","clinical_significance":[],"alleles":["T","C"],"end":140512530,"strand":1,"feature_type":"variation","start":140512530,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140512531,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140512531,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1254596958","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512533,"feature_type":"variation","strand":1,"end":140512533,"alleles":["C","G","T"],"clinical_significance":[],"id":"rs1042233995","seq_region_name":"7"},{"alleles":["C","T"],"end":140512534,"strand":1,"feature_type":"variation","start":140512534,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795652988","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512534,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CAGGGCAGGG","CAGGG"],"end":140512543,"seq_region_name":"7","id":"rs1795653008","clinical_significance":[]},{"end":140512544,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140512544,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs907278899","clinical_significance":[]},{"id":"rs898606064","seq_region_name":"7","clinical_significance":[],"start":140512546,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140512546,"alleles":["G","A","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795653074","alleles":["GGGGG","GGGGGG"],"end":140512550,"feature_type":"variation","strand":1,"source":"dbSNP","start":140512546,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["GGGATGGTGGCAGGGTGAGGG","GGG"],"end":140512568,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512548,"clinical_significance":[],"id":"rs1795653096","seq_region_name":"7"},{"end":140512551,"alleles":["A","-"],"strand":1,"feature_type":"variation","start":140512551,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1299542348","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140512557,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140512557,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1281301983","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140512558,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512558,"clinical_significance":[],"seq_region_name":"7","id":"rs1795653134"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795653152","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512561,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140512561},{"id":"rs1249438714","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140512562,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512562,"source":"dbSNP"},{"start":140512563,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C","G"],"end":140512563,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs994239873","clinical_significance":[]},{"seq_region_name":"7","id":"rs938882026","clinical_significance":[],"end":140512565,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140512565,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140512566,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512566,"clinical_significance":[],"id":"rs1055870945","seq_region_name":"7"},{"id":"rs894626273","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140512570,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512570,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1795653267","seq_region_name":"7","feature_type":"variation","strand":1,"end":140512571,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512571},{"strand":1,"feature_type":"variation","end":140512573,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512573,"source":"dbSNP","seq_region_name":"7","id":"rs1795653300","clinical_significance":[]},{"seq_region_name":"7","id":"rs995730579","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512574,"source":"dbSNP","strand":1,"feature_type":"variation","end":140512574,"alleles":["G","A"]},{"start":140512584,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140512584,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","id":"rs1795653355","seq_region_name":"7","clinical_significance":[]},{"start":140512585,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140512585,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130431477","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130431481","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512587,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140512587},{"seq_region_name":"7","id":"rs1422812740","clinical_significance":[],"end":140512590,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140512590,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512591,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C","T"],"end":140512591,"id":"rs10249780","seq_region_name":"7","clinical_significance":[]},{"start":140512594,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140512594,"strand":1,"feature_type":"variation","id":"rs1265203228","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","A"],"end":140512596,"strand":1,"feature_type":"variation","start":140512596,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1214607017","clinical_significance":[]},{"id":"rs891317472","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140512597,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512597,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795653571","clinical_significance":[],"end":140512599,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140512599,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140512600,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140512600,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs886778866"},{"seq_region_name":"7","id":"rs1795653623","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512602,"source":"dbSNP","strand":1,"feature_type":"variation","end":140512602,"alleles":["C","A"]},{"clinical_significance":[],"id":"rs1795653644","seq_region_name":"7","source":"dbSNP","start":140512602,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["CC","C"],"end":140512603,"feature_type":"variation","strand":1},{"start":140512603,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","G"],"end":140512603,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1008359378","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795653689","source":"dbSNP","start":140512606,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140512606,"alleles":["T","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795653712","clinical_significance":[],"strand":1,"feature_type":"variation","end":140512607,"alleles":["T","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512607,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1310655017","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140512608,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512608},{"clinical_significance":[],"id":"rs1283120681","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512612,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140512612},{"clinical_significance":[],"id":"rs1795653794","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512617,"feature_type":"variation","strand":1,"end":140512617,"alleles":["C","T"]},{"id":"rs1003877882","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512618,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140512618},{"start":140512619,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140512619,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795653866","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140512634,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512634,"clinical_significance":[],"seq_region_name":"7","id":"rs1342989172"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795653894","feature_type":"variation","strand":1,"end":140512637,"alleles":["-","AT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512638},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795653916","end":140512640,"alleles":["GG","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140512639,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140512641,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512641,"clinical_significance":[],"seq_region_name":"7","id":"rs549762150"},{"source":"dbSNP","start":140512648,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["GG","G"],"end":140512649,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1173777943","seq_region_name":"7"},{"start":140512654,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140512654,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795653981","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1382120706","alleles":["C","T"],"end":140512656,"feature_type":"variation","strand":1,"source":"dbSNP","start":140512656,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs55787138","clinical_significance":[],"start":140512660,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140512660,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1302862698","source":"dbSNP","start":140512661,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140512661,"feature_type":"variation","strand":1},{"end":140512662,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140512662,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs187726170"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512663,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140512663,"id":"rs2130431551","seq_region_name":"7","clinical_significance":[]},{"end":140512665,"alleles":["GG","G"],"strand":1,"feature_type":"variation","start":140512664,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795654175","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140512668,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512668,"source":"dbSNP","seq_region_name":"7","id":"rs1321477468","clinical_significance":[]},{"alleles":["G","A"],"end":140512669,"feature_type":"variation","strand":1,"source":"dbSNP","start":140512669,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130431558"},{"seq_region_name":"7","id":"rs144244200","clinical_significance":[],"strand":1,"feature_type":"variation","end":140512670,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512670,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512677,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140512677,"seq_region_name":"7","id":"rs1465926299","clinical_significance":[]},{"clinical_significance":[],"id":"rs2130431566","seq_region_name":"7","end":140512678,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140512678,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140512681,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512681,"source":"dbSNP","seq_region_name":"7","id":"rs1795654273","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512686,"feature_type":"variation","strand":1,"end":140512686,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs566203618"},{"source":"dbSNP","start":140512687,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140512687,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs957828599","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512690,"source":"dbSNP","strand":1,"feature_type":"variation","end":140512690,"alleles":["G","A"],"id":"rs989810643","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs2130431580","seq_region_name":"7","feature_type":"variation","strand":1,"end":140512695,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512695},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140512700,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512700,"source":"dbSNP","id":"rs1795654394","seq_region_name":"7","clinical_significance":[]},{"end":140512701,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140512701,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1427779640","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs539911272","source":"dbSNP","start":140512704,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140512704,"feature_type":"variation","strand":1},{"id":"rs73490402","seq_region_name":"7","clinical_significance":[],"start":140512705,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140512705,"strand":1,"feature_type":"variation"},{"alleles":["G","A"],"end":140512706,"strand":1,"feature_type":"variation","start":140512706,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs977831833","clinical_significance":[]},{"clinical_significance":[],"id":"rs946074570","seq_region_name":"7","source":"dbSNP","start":140512709,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140512709,"alleles":["A","T"],"feature_type":"variation","strand":1},{"id":"rs1262726289","seq_region_name":"7","clinical_significance":[],"alleles":["G","T"],"end":140512711,"strand":1,"feature_type":"variation","start":140512711,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1281836550","seq_region_name":"7","clinical_significance":[],"start":140512712,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140512712,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1585528189","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512714,"source":"dbSNP","strand":1,"feature_type":"variation","end":140512714,"alleles":["G","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512716,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140512716,"clinical_significance":[],"seq_region_name":"7","id":"rs569906422"},{"start":140512720,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140512720,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs923655354","clinical_significance":[]},{"id":"rs2130431607","seq_region_name":"7","clinical_significance":[],"alleles":["C","G"],"end":140512722,"strand":1,"feature_type":"variation","start":140512722,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140512731,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140512731,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1256488798","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs768998767","end":140512732,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140512732,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140512737,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512737,"source":"dbSNP","seq_region_name":"7","id":"rs1795654811","clinical_significance":[]},{"alleles":["A","G"],"end":140512739,"strand":1,"feature_type":"variation","start":140512739,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795654843","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795654865","feature_type":"variation","strand":1,"alleles":["T","A"],"end":140512743,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512743},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130431625","source":"dbSNP","start":140512744,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140512744,"alleles":["G","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1312889951","clinical_significance":[],"strand":1,"feature_type":"variation","end":140512746,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512746,"source":"dbSNP"},{"alleles":["C","A","T"],"end":140512747,"strand":1,"feature_type":"variation","start":140512747,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1209677901","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130431635","feature_type":"variation","strand":1,"end":140512749,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512749},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512759,"feature_type":"variation","strand":1,"alleles":["G","C","T"],"end":140512759,"clinical_significance":[],"seq_region_name":"7","id":"rs1795654939"},{"start":140512762,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140512762,"alleles":["A","G"],"strand":1,"feature_type":"variation","id":"rs1585528207","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs992395415","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140512765,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512765},{"seq_region_name":"7","id":"rs781730679","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512767,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140512767},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512769,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140512769,"id":"rs376731893","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512770,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140512770,"clinical_significance":[],"seq_region_name":"7","id":"rs1444874017"},{"feature_type":"variation","strand":1,"end":140512772,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512772,"clinical_significance":[],"seq_region_name":"7","id":"rs1447011300"},{"clinical_significance":[],"id":"rs1214505532","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512774,"feature_type":"variation","strand":1,"end":140512774,"alleles":["T","A"]},{"alleles":["G","C"],"end":140512779,"strand":1,"feature_type":"variation","start":140512779,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1165878792","clinical_significance":[]},{"end":140512782,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140512782,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs551847899"},{"seq_region_name":"7","id":"rs1795655323","clinical_significance":[],"strand":1,"feature_type":"variation","end":140512783,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512783,"source":"dbSNP"},{"alleles":["G","A"],"end":140512786,"feature_type":"variation","strand":1,"source":"dbSNP","start":140512786,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1368955815","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1167066400","seq_region_name":"7","end":140512791,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140512791,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140512794,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140512794,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs938787843","clinical_significance":[]},{"source":"dbSNP","start":140512800,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140512800,"alleles":["T","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1055780282"},{"clinical_significance":[],"id":"rs1189417006","seq_region_name":"7","source":"dbSNP","start":140512804,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140512804,"alleles":["G","A"],"feature_type":"variation","strand":1},{"alleles":["A","G"],"end":140512806,"feature_type":"variation","strand":1,"source":"dbSNP","start":140512806,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130431677"},{"strand":1,"feature_type":"variation","end":140512809,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512809,"source":"dbSNP","seq_region_name":"7","id":"rs1795655508","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512812,"source":"dbSNP","strand":1,"feature_type":"variation","end":140512812,"alleles":["G","A"],"id":"rs1179506663","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1459216376","feature_type":"variation","strand":1,"end":140512814,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512814},{"strand":1,"feature_type":"variation","end":140512815,"alleles":["A","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512815,"source":"dbSNP","seq_region_name":"7","id":"rs1795655583","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140512816,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512816,"clinical_significance":[],"seq_region_name":"7","id":"rs1236797947"},{"alleles":["C","G"],"end":140512820,"strand":1,"feature_type":"variation","start":140512820,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs894657363","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795655660","clinical_significance":[],"alleles":["T","C"],"end":140512821,"strand":1,"feature_type":"variation","start":140512821,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1357719636","alleles":["G","A"],"end":140512822,"feature_type":"variation","strand":1,"source":"dbSNP","start":140512822,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1795655709","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140512829,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512829,"source":"dbSNP"},{"start":140512832,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140512832,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1428433486","clinical_significance":[]},{"alleles":["G","A"],"end":140512833,"feature_type":"variation","strand":1,"source":"dbSNP","start":140512833,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795655778"},{"alleles":["G","T"],"end":140512835,"feature_type":"variation","strand":1,"source":"dbSNP","start":140512835,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795655797","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512837,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140512837,"id":"rs1795655822","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512845,"source":"dbSNP","strand":1,"feature_type":"variation","end":140512845,"alleles":["T","C"],"seq_region_name":"7","id":"rs1356683615","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512846,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140512846,"seq_region_name":"7","id":"rs563870751","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795655903","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512848,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140512848},{"seq_region_name":"7","id":"rs79177493","clinical_significance":[],"start":140512850,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G","T"],"end":140512850,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1652992816","end":140512851,"alleles":["AA","AAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140512850,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140512854,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512854,"clinical_significance":[],"seq_region_name":"7","id":"rs929937538"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1049163382","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512855,"feature_type":"variation","strand":1,"end":140512855,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs574261897","clinical_significance":[],"end":140512858,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140512858,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1391167543","source":"dbSNP","start":140512860,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140512860,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1585528277","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512869,"feature_type":"variation","strand":1,"end":140512869,"alleles":["A","C","G"]},{"seq_region_name":"7","id":"rs1391122793","clinical_significance":[],"strand":1,"feature_type":"variation","end":140512870,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512870,"source":"dbSNP"},{"id":"rs1563109536","seq_region_name":"7","clinical_significance":[],"start":140512876,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140512876,"strand":1,"feature_type":"variation"},{"start":140512882,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140512882,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1399139977","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1422602721","source":"dbSNP","start":140512884,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C","G"],"end":140512884,"feature_type":"variation","strand":1},{"end":140512886,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140512886,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs76378882"},{"alleles":["C","T"],"end":140512887,"strand":1,"feature_type":"variation","start":140512887,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130431754","clinical_significance":[]},{"end":140512888,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140512888,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1004311948","seq_region_name":"7"},{"end":140512889,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140512889,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795656331"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1019256791","source":"dbSNP","start":140512892,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140512892,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140512895,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140512895,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1441844415"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512897,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140512897,"seq_region_name":"7","id":"rs900815086","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795656441","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140512898,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512898,"source":"dbSNP"},{"start":140512905,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140512905,"alleles":["G","C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs74889382","clinical_significance":[]},{"alleles":["C","G","T"],"end":140512908,"feature_type":"variation","strand":1,"source":"dbSNP","start":140512908,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1040271614","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512909,"feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140512909,"clinical_significance":[],"id":"rs1208583188","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795656571","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140512914,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512914,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1290474154","seq_region_name":"7","source":"dbSNP","start":140512915,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140512915,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512916,"source":"dbSNP","strand":1,"feature_type":"variation","end":140512919,"alleles":["TTTT","TTT","TTTTT"],"seq_region_name":"7","id":"rs1490312502","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130431786","clinical_significance":[],"start":140512920,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140512920,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"end":140512927,"alleles":["TGCT","T"],"strand":1,"feature_type":"variation","start":140512924,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795656663","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585528309","clinical_significance":[],"strand":1,"feature_type":"variation","end":140512925,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512925,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795656718","clinical_significance":[],"end":140512925,"alleles":["-","TTT"],"strand":1,"feature_type":"variation","start":140512926,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1331481332","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512926,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140512926},{"id":"rs1438630648","seq_region_name":"7","clinical_significance":[],"alleles":["C","-"],"end":140512926,"strand":1,"feature_type":"variation","start":140512926,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795656796","clinical_significance":[],"alleles":["T","C"],"end":140512927,"strand":1,"feature_type":"variation","start":140512927,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["TTTTTTTTTTTTTTTT","TTTTTTTTTTT","TTTTTTTTTTTT","TTTTTTTTTTTTT","TTTTTTTTTTTTTT","TTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTT"],"end":140512942,"feature_type":"variation","strand":1,"source":"dbSNP","start":140512927,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs777228178"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512931,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140512931,"seq_region_name":"7","id":"rs1795656960","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512934,"source":"dbSNP","strand":1,"feature_type":"variation","end":140512934,"alleles":["T","C"],"seq_region_name":"7","id":"rs1795656987","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","TCT"],"end":140512935,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512935,"clinical_significance":[],"seq_region_name":"7","id":"rs900103838"},{"source":"dbSNP","start":140512942,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140512942,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1298922379"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1421565304","alleles":["-","TA"],"end":140512942,"feature_type":"variation","strand":1,"source":"dbSNP","start":140512943,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140512943,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140512943,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1345391040","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795657121","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512943,"feature_type":"variation","strand":1,"alleles":["AA","A"],"end":140512944},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512943,"feature_type":"variation","strand":1,"end":140512944,"alleles":["AA","-"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795657142"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512944,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140512944,"id":"rs116152268","seq_region_name":"7","clinical_significance":[]},{"start":140512945,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140512945,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1012227415","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1385561082","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512949,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140512949},{"source":"dbSNP","start":140512949,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140512950,"alleles":["GA","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1290563168"},{"clinical_significance":[],"id":"rs907537257","seq_region_name":"7","source":"dbSNP","start":140512950,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G","T"],"end":140512950,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795657417","clinical_significance":[],"end":140512954,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140512954,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1290076449","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512955,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140512955},{"feature_type":"variation","strand":1,"end":140512956,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512956,"clinical_significance":[],"seq_region_name":"7","id":"rs1452840722"},{"seq_region_name":"7","id":"rs1219574255","clinical_significance":[],"alleles":["C","A"],"end":140512960,"strand":1,"feature_type":"variation","start":140512960,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795657538","alleles":["G","T"],"end":140512964,"feature_type":"variation","strand":1,"source":"dbSNP","start":140512964,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1264504279","end":140512965,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140512965,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140512966,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512966,"source":"dbSNP","seq_region_name":"7","id":"rs1585528383","clinical_significance":[]},{"end":140512968,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140512968,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1219368228","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795657639","clinical_significance":[],"start":140512969,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140512969,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512971,"source":"dbSNP","strand":1,"feature_type":"variation","end":140512971,"alleles":["G","A"],"seq_region_name":"7","id":"rs1795657665","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140512973,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512973,"source":"dbSNP","seq_region_name":"7","id":"rs1795657697","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512976,"source":"dbSNP","strand":1,"feature_type":"variation","end":140512976,"alleles":["G","A"],"seq_region_name":"7","id":"rs1795657723","clinical_significance":[]},{"seq_region_name":"7","id":"rs1489003398","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512977,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140512977},{"source":"dbSNP","start":140512982,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140512982,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs571825311"},{"clinical_significance":[],"id":"rs2130431864","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512983,"feature_type":"variation","strand":1,"end":140512983,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1204203755","source":"dbSNP","start":140512985,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140512985,"alleles":["T","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1021857018","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512990,"source":"dbSNP","strand":1,"feature_type":"variation","end":140512990,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1795657859","clinical_significance":[],"alleles":["A","G"],"end":140512994,"strand":1,"feature_type":"variation","start":140512994,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140512997,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140512997,"source":"dbSNP","seq_region_name":"7","id":"rs1257616579","clinical_significance":[]},{"clinical_significance":[],"id":"rs1483331737","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140512998,"feature_type":"variation","strand":1,"end":140512998,"alleles":["G","A","C"]},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140513001,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513001,"source":"dbSNP","id":"rs1795657978","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140513003,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140513003,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1184122131"},{"seq_region_name":"7","id":"rs1361842021","clinical_significance":[],"start":140513004,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140513004,"strand":1,"feature_type":"variation"},{"alleles":["C","A","T"],"end":140513007,"strand":1,"feature_type":"variation","start":140513007,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs967691780","clinical_significance":[]},{"seq_region_name":"7","id":"rs1415313799","clinical_significance":[],"end":140513008,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140513008,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513011,"feature_type":"variation","strand":1,"end":140513011,"alleles":["G","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1404612803"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1174786673","source":"dbSNP","start":140513018,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140513018,"alleles":["A","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs545452750","feature_type":"variation","strand":1,"end":140513019,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513019},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140513024,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513024,"source":"dbSNP","seq_region_name":"7","id":"rs1795658186","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513030,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140513030,"clinical_significance":[],"seq_region_name":"7","id":"rs192633207"},{"start":140513033,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140513033,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs1414716839","seq_region_name":"7","clinical_significance":[]},{"end":140513034,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140513034,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs2130431907","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs575999397","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513036,"feature_type":"variation","strand":1,"end":140513036,"alleles":["C","T"]},{"start":140513037,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140513039,"alleles":["TTT","TTTT"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795658683","clinical_significance":[]},{"start":140513040,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140513042,"alleles":["GGG","GG"],"strand":1,"feature_type":"variation","id":"rs1795658706","seq_region_name":"7","clinical_significance":[]},{"start":140513042,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140513042,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795658720","clinical_significance":[]},{"clinical_significance":[],"id":"rs543396268","seq_region_name":"7","end":140513046,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140513046,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["T","A","C","G"],"end":140513047,"strand":1,"feature_type":"variation","start":140513047,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs561868522","clinical_significance":[]},{"end":140513052,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140513052,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs529162313","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795658859","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513054,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140513054},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513055,"source":"dbSNP","strand":1,"feature_type":"variation","end":140513055,"alleles":["G","T"],"seq_region_name":"7","id":"rs540054669","clinical_significance":[]},{"alleles":["C","T"],"end":140513056,"feature_type":"variation","strand":1,"source":"dbSNP","start":140513056,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1334367282"},{"seq_region_name":"7","id":"rs183542928","clinical_significance":[],"end":140513057,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140513057,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140513064,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513064,"source":"dbSNP","seq_region_name":"7","id":"rs200001329","clinical_significance":[]},{"source":"dbSNP","start":140513064,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140513065,"alleles":["CT","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1284460940","seq_region_name":"7"},{"id":"rs187502631","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140513073,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513073,"source":"dbSNP"},{"start":140513077,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A","C","G"],"end":140513077,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1243209767","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513079,"source":"dbSNP","strand":1,"feature_type":"variation","end":140513079,"alleles":["C","G","T"],"seq_region_name":"7","id":"rs992028883","clinical_significance":[]},{"alleles":["G","A"],"end":140513080,"feature_type":"variation","strand":1,"source":"dbSNP","start":140513080,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs533472759"},{"seq_region_name":"7","id":"rs1795659168","clinical_significance":[],"start":140513081,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140513081,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"id":"rs1585528430","seq_region_name":"7","clinical_significance":[],"start":140513083,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140513083,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs192742001","seq_region_name":"7","source":"dbSNP","start":140513085,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140513085,"alleles":["C","T"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513087,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140513087,"id":"rs1207192671","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795659290","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513088,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140513088},{"seq_region_name":"7","id":"rs969220718","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513090,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140513090},{"seq_region_name":"7","id":"rs1248253589","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513094,"source":"dbSNP","strand":1,"feature_type":"variation","end":140513094,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs572080859","source":"dbSNP","start":140513102,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140513102,"alleles":["T","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1437019461","source":"dbSNP","start":140513103,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140513103,"alleles":["G","A"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513107,"source":"dbSNP","strand":1,"feature_type":"variation","end":140513107,"alleles":["C","A","T"],"id":"rs570128613","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1187949399","source":"dbSNP","start":140513107,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140513110,"alleles":["CCCC","CCC","CCCCC"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1408785825","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140513108,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513108},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513109,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140513109,"clinical_significance":[],"seq_region_name":"7","id":"rs184593324"},{"alleles":["C","T"],"end":140513110,"strand":1,"feature_type":"variation","start":140513110,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1181896799","clinical_significance":[]},{"source":"dbSNP","start":140513111,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140513111,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs558102019"},{"feature_type":"variation","strand":1,"end":140513112,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513112,"clinical_significance":[],"seq_region_name":"7","id":"rs1244396896"},{"seq_region_name":"7","id":"rs567886830","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513113,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140513113},{"clinical_significance":[],"seq_region_name":"7","id":"rs200856321","end":140513116,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140513116,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140513117,"alleles":["A","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513117,"source":"dbSNP","seq_region_name":"7","id":"rs1238623719","clinical_significance":[]},{"seq_region_name":"7","id":"rs1206351166","clinical_significance":[],"start":140513120,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140513120,"strand":1,"feature_type":"variation"},{"start":140513121,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140513121,"alleles":["A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1409777744","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795659831","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140513124,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513124,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1272232801","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140513125,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513125},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140513127,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513127,"source":"dbSNP","seq_region_name":"7","id":"rs1795659928","clinical_significance":[]},{"source":"dbSNP","start":140513129,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140513129,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs2130432014","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795659961","end":140513135,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140513135,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513138,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140513138,"id":"rs11769715","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs571459507","clinical_significance":[],"end":140513139,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140513139,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1450001173","clinical_significance":[],"end":140513140,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140513140,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513142,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140513142,"clinical_significance":[],"seq_region_name":"7","id":"rs1245598022"},{"seq_region_name":"7","id":"rs1313809936","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140513143,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513143,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140513148,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513148,"clinical_significance":[],"seq_region_name":"7","id":"rs1795660265"},{"id":"rs912689548","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","AA"],"end":140513151,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513151,"source":"dbSNP"},{"id":"rs1354258619","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513151,"source":"dbSNP","strand":1,"feature_type":"variation","end":140513151,"alleles":["A","T"]},{"clinical_significance":[],"id":"rs1324813704","seq_region_name":"7","source":"dbSNP","start":140513152,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140513152,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs763211374","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513153,"source":"dbSNP","strand":1,"feature_type":"variation","end":140513153,"alleles":["G","C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1386568928","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140513154,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513154},{"start":140513156,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140513156,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130432045","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140513158,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513158,"source":"dbSNP","seq_region_name":"7","id":"rs1795660436","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795660462","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513162,"feature_type":"variation","strand":1,"end":140513162,"alleles":["G","A"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513166,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140513166,"seq_region_name":"7","id":"rs1585528488","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795660519","clinical_significance":[],"start":140513175,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140513175,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"start":140513180,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140513180,"strand":1,"feature_type":"variation","id":"rs1585528491","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140513183,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513183,"source":"dbSNP","seq_region_name":"7","id":"rs1795660563","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140513189,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513189,"source":"dbSNP","seq_region_name":"7","id":"rs1249576511","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795660618","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513190,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140513190},{"seq_region_name":"7","id":"rs1039899290","clinical_significance":[],"strand":1,"feature_type":"variation","end":140513191,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513191,"source":"dbSNP"},{"seq_region_name":"7","id":"rs111403544","clinical_significance":[],"strand":1,"feature_type":"variation","end":140513195,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513195,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795660737","alleles":["T","C"],"end":140513200,"feature_type":"variation","strand":1,"source":"dbSNP","start":140513200,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140513202,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140513202,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795660764","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795660793","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513205,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140513205},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513206,"source":"dbSNP","strand":1,"feature_type":"variation","end":140513206,"alleles":["C","T"],"seq_region_name":"7","id":"rs1178528380","clinical_significance":[]},{"clinical_significance":[],"id":"rs1468438292","seq_region_name":"7","source":"dbSNP","start":140513213,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140513213,"alleles":["C","T"],"feature_type":"variation","strand":1},{"start":140513214,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140513214,"alleles":["A","G"],"strand":1,"feature_type":"variation","id":"rs1795660866","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140513217,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513217,"clinical_significance":[],"seq_region_name":"7","id":"rs1232029341"},{"end":140513219,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140513219,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585528507","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585528510","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513225,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140513225},{"feature_type":"variation","strand":1,"end":140513232,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513232,"clinical_significance":[],"seq_region_name":"7","id":"rs1795660970"},{"end":140513242,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140513242,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795660999"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140513246,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513246,"source":"dbSNP","seq_region_name":"7","id":"rs1795661021","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140513247,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513247,"source":"dbSNP","seq_region_name":"7","id":"rs1585528514","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1490817388","feature_type":"variation","strand":1,"end":140513248,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513248},{"seq_region_name":"7","id":"rs1795661107","clinical_significance":[],"alleles":["T","C"],"end":140513249,"strand":1,"feature_type":"variation","start":140513249,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1289771519","clinical_significance":[],"start":140513250,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140513250,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513252,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140513252,"clinical_significance":[],"seq_region_name":"7","id":"rs1200873049"},{"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140513254,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513254,"source":"dbSNP","seq_region_name":"7","id":"rs1280435370","clinical_significance":[]},{"alleles":["C","T"],"end":140513255,"feature_type":"variation","strand":1,"source":"dbSNP","start":140513255,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795661223"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1354754461","alleles":["G","A","T"],"end":140513258,"feature_type":"variation","strand":1,"source":"dbSNP","start":140513258,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1181994260","source":"dbSNP","start":140513261,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140513261,"alleles":["A","C","G"],"feature_type":"variation","strand":1},{"alleles":["ACA","A"],"end":140513264,"strand":1,"feature_type":"variation","start":140513262,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795661310","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1242692083","clinical_significance":[],"start":140513264,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140513264,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"id":"rs1450204796","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513265,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140513265},{"seq_region_name":"7","id":"rs1795661396","clinical_significance":[],"start":140513265,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140513271,"alleles":["GAGTGAG","GAG"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1195360712","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513268,"feature_type":"variation","strand":1,"end":140513268,"alleles":["T","C","G"]},{"alleles":["G","A"],"end":140513269,"strand":1,"feature_type":"variation","start":140513269,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1371904814","clinical_significance":[]},{"seq_region_name":"7","id":"rs1475358468","clinical_significance":[],"alleles":["C","A","T"],"end":140513273,"strand":1,"feature_type":"variation","start":140513273,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140513276,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140513276,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1173592507","clinical_significance":[]},{"seq_region_name":"7","id":"rs1408736624","clinical_significance":[],"start":140513277,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140513277,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1795661558","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140513278,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513278,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795661595","feature_type":"variation","strand":1,"alleles":["-","A"],"end":140513280,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513281},{"alleles":["C","A"],"end":140513281,"strand":1,"feature_type":"variation","start":140513281,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1300788677","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795661640","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","-"],"end":140513281,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513281},{"strand":1,"feature_type":"variation","end":140513282,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513282,"source":"dbSNP","seq_region_name":"7","id":"rs1585528545","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140513293,"alleles":["AAAAAAAAAAAA","AAAAAAAAAA","AAAAAAAAAAA","AAAAAAAAAAAAA","AAAAAAAAAAAAAA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513282,"source":"dbSNP","id":"rs111911570","seq_region_name":"7","clinical_significance":[]},{"id":"rs1795661844","seq_region_name":"7","clinical_significance":[],"start":140513292,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140513292,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795661870","source":"dbSNP","start":140513294,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140513294,"alleles":["T","-"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140513296,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513296,"clinical_significance":[],"seq_region_name":"7","id":"rs181721926"},{"seq_region_name":"7","id":"rs1795661968","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513303,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140513303},{"id":"rs1795661989","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140513304,"strand":1,"feature_type":"variation","start":140513304,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140513306,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513306,"source":"dbSNP","seq_region_name":"7","id":"rs1043300073","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs184693559","source":"dbSNP","start":140513307,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140513307,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795662089","feature_type":"variation","strand":1,"end":140513316,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513316},{"seq_region_name":"7","id":"rs1198542364","clinical_significance":[],"strand":1,"feature_type":"variation","end":140513318,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513318,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1488674006","source":"dbSNP","start":140513319,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140513319,"feature_type":"variation","strand":1},{"start":140513322,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140513322,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130432230","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513323,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140513323,"clinical_significance":[],"seq_region_name":"7","id":"rs903439677"},{"seq_region_name":"7","id":"rs1795662225","clinical_significance":[],"alleles":["C","A"],"end":140513330,"strand":1,"feature_type":"variation","start":140513330,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140513332,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513332,"source":"dbSNP","seq_region_name":"7","id":"rs1316540083","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795662266","clinical_significance":[],"end":140513333,"alleles":["C","-"],"strand":1,"feature_type":"variation","start":140513333,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs999187948","clinical_significance":[],"start":140513339,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140513339,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513343,"feature_type":"variation","strand":1,"end":140513343,"alleles":["G","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1436670654"},{"seq_region_name":"7","id":"rs1585528580","clinical_significance":[],"start":140513344,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140513344,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1585528582","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140513345,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513345,"source":"dbSNP"},{"alleles":["C","A","T"],"end":140513351,"strand":1,"feature_type":"variation","start":140513351,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs370190351","clinical_significance":[]},{"seq_region_name":"7","id":"rs189406296","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140513352,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513352,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795662491","feature_type":"variation","strand":1,"end":140513353,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513353},{"alleles":["T","G"],"end":140513359,"feature_type":"variation","strand":1,"source":"dbSNP","start":140513359,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795662515"},{"source":"dbSNP","start":140513362,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140513362,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795662535"},{"end":140513363,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140513363,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1283241937"},{"alleles":["A","T"],"end":140513364,"strand":1,"feature_type":"variation","start":140513364,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795662571","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795662593","end":140513366,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140513366,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1325825346","clinical_significance":[],"start":140513375,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140513375,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1401072092","source":"dbSNP","start":140513376,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140513376,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140513377,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513377,"source":"dbSNP","id":"rs1362062041","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1290105172","source":"dbSNP","start":140513379,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140513379,"alleles":["G","A"],"feature_type":"variation","strand":1},{"id":"rs1451266356","seq_region_name":"7","clinical_significance":[],"start":140513381,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140513381,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795662725","source":"dbSNP","start":140513384,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140513384,"feature_type":"variation","strand":1},{"start":140513385,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140513385,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs1795662746","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","C"],"end":140513391,"feature_type":"variation","strand":1,"source":"dbSNP","start":140513391,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795662756"},{"id":"rs1795662772","seq_region_name":"7","clinical_significance":[],"end":140513395,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140513395,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513396,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140513396,"clinical_significance":[],"id":"rs1344209214","seq_region_name":"7"},{"id":"rs1795662807","seq_region_name":"7","clinical_significance":[],"start":140513399,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140513399,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1563109659","clinical_significance":[],"start":140513400,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G","T"],"end":140513400,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140513405,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140513405,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795662843"},{"seq_region_name":"7","id":"rs1795662870","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140513406,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513406,"source":"dbSNP"},{"end":140513407,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140513407,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1233865194","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795662913","alleles":["G","C"],"end":140513408,"feature_type":"variation","strand":1,"source":"dbSNP","start":140513408,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795662921","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513413,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140513413},{"source":"dbSNP","start":140513417,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AAAAA","AAAA"],"end":140513421,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1563109664","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513419,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140513419,"clinical_significance":[],"seq_region_name":"7","id":"rs1176590975"},{"source":"dbSNP","start":140513422,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140513422,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1563109671"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513423,"feature_type":"variation","strand":1,"end":140513423,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1563109673"},{"alleles":["C","T"],"end":140513424,"feature_type":"variation","strand":1,"source":"dbSNP","start":140513424,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795662993"},{"clinical_significance":[],"seq_region_name":"7","id":"rs896266512","feature_type":"variation","strand":1,"end":140513431,"alleles":["AAAAAAA","AAAAAA","AAAAAAAA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513425},{"clinical_significance":[],"id":"rs1175619150","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513431,"feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140513431},{"source":"dbSNP","start":140513434,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140513434,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1013766289"},{"seq_region_name":"7","id":"rs1795663084","clinical_significance":[],"end":140513438,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140513438,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1321158156","clinical_significance":[],"strand":1,"feature_type":"variation","end":140513441,"alleles":["T","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513441,"source":"dbSNP"},{"seq_region_name":"7","id":"rs867326626","clinical_significance":[],"start":140513446,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140513446,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"end":140513449,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140513449,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1264015415"},{"clinical_significance":[],"seq_region_name":"7","id":"rs555312012","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140513450,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513450},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795663193","source":"dbSNP","start":140513451,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140513451,"feature_type":"variation","strand":1},{"end":140513452,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140513452,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795663218","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1262780466","source":"dbSNP","start":140513453,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140513453,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140513454,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140513454,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs9770740"},{"alleles":["C","A"],"end":140513455,"feature_type":"variation","strand":1,"source":"dbSNP","start":140513455,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs575033646"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1259743760","source":"dbSNP","start":140513457,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140513457,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513459,"feature_type":"variation","strand":1,"end":140513459,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs182013874"},{"source":"dbSNP","start":140513464,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140513464,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795663391"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1026935796","alleles":["C","T"],"end":140513465,"feature_type":"variation","strand":1,"source":"dbSNP","start":140513465,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs186508757","seq_region_name":"7","clinical_significance":[],"end":140513470,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140513470,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1309779244","seq_region_name":"7","end":140513471,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140513471,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1297155957","seq_region_name":"7","source":"dbSNP","start":140513473,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140513473,"alleles":["T","A"],"feature_type":"variation","strand":1},{"end":140513479,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140513479,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795663516","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795663545","seq_region_name":"7","alleles":["T","C"],"end":140513480,"feature_type":"variation","strand":1,"source":"dbSNP","start":140513480,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140513519,"alleles":["GAGGCAGGAGAATGGTGTGGAGGCAGGAGAATGGTGTG","GAGGCAGGAGAATGGTGTG","GAGGCAGGAGAATGGTGTGGAGGCAGGAGAATGGTGTGGAGGCAGGAGAATGGTGTG"],"strand":1,"feature_type":"variation","start":140513482,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1380007383","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795663618","alleles":["G","T"],"end":140513485,"feature_type":"variation","strand":1,"source":"dbSNP","start":140513485,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","G"],"end":140513486,"strand":1,"feature_type":"variation","start":140513486,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795663640","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs545210545","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513488,"feature_type":"variation","strand":1,"end":140513488,"alleles":["G","A"]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140513489,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513489,"source":"dbSNP","seq_region_name":"7","id":"rs2130432395","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795663687","alleles":["A","G"],"end":140513490,"feature_type":"variation","strand":1,"source":"dbSNP","start":140513490,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1454184023","clinical_significance":[],"alleles":["G","A"],"end":140513495,"strand":1,"feature_type":"variation","start":140513495,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140513496,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140513496,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795663721"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795663739","feature_type":"variation","strand":1,"end":140513500,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513500},{"feature_type":"variation","strand":1,"end":140513501,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513501,"clinical_significance":[],"seq_region_name":"7","id":"rs1795663751"},{"strand":1,"feature_type":"variation","end":140513507,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513507,"source":"dbSNP","id":"rs1795663771","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513512,"source":"dbSNP","strand":1,"feature_type":"variation","end":140513512,"alleles":["A","G"],"id":"rs1403646629","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795663814","end":140513513,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140513513,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140513519,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140513519,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795663834","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585528679","alleles":["A","C"],"end":140513521,"feature_type":"variation","strand":1,"source":"dbSNP","start":140513521,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1175424500","clinical_significance":[],"alleles":["G","C"],"end":140513526,"strand":1,"feature_type":"variation","start":140513526,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140513528,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140513528,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795663885","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795663902","feature_type":"variation","strand":1,"end":140513529,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513529},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795663928","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513531,"feature_type":"variation","strand":1,"end":140513531,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1755274481","clinical_significance":[],"alleles":["A","G"],"end":140513532,"strand":1,"feature_type":"variation","start":140513532,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140513535,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140513535,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795663944"},{"feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140513538,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513538,"clinical_significance":[],"seq_region_name":"7","id":"rs1795663961"},{"clinical_significance":[],"id":"rs912551926","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140513540,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513540},{"start":140513543,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140513543,"strand":1,"feature_type":"variation","id":"rs532442605","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140513544,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513544,"clinical_significance":[],"seq_region_name":"7","id":"rs1795664036"},{"clinical_significance":[],"seq_region_name":"7","id":"rs975907726","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140513545,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513545},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513547,"source":"dbSNP","strand":1,"feature_type":"variation","end":140513547,"alleles":["C","A"],"id":"rs1795664088","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140513548,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140513548,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1428018312"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513549,"source":"dbSNP","strand":1,"feature_type":"variation","end":140513549,"alleles":["G","A"],"seq_region_name":"7","id":"rs1414543201","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795664129","source":"dbSNP","start":140513552,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140513552,"feature_type":"variation","strand":1},{"end":140513553,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140513553,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs766835013","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795664151","source":"dbSNP","start":140513555,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140513555,"alleles":["A","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1563109707","clinical_significance":[],"start":140513558,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140513558,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140513561,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140513561,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795664182"},{"seq_region_name":"7","id":"rs1795664206","clinical_significance":[],"start":140513563,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140513563,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513567,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140513567,"id":"rs2130432448","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795664232","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513571,"feature_type":"variation","strand":1,"end":140513571,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1795664253","clinical_significance":[],"start":140513572,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140513572,"strand":1,"feature_type":"variation"},{"id":"rs1185672406","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["GGG","GG"],"end":140513577,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513575,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1460141535","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513577,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140513577},{"seq_region_name":"7","id":"rs754144085","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140513578,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513578,"source":"dbSNP"},{"end":140513579,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140513579,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1481936497"},{"seq_region_name":"7","id":"rs563663482","clinical_significance":[],"strand":1,"feature_type":"variation","end":140513581,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513581,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1383636409","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140513582,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513582},{"clinical_significance":[],"id":"rs2130432472","seq_region_name":"7","source":"dbSNP","start":140513583,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140513583,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795664463","source":"dbSNP","start":140513585,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140513585,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140513586,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140513586,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs372029561"},{"seq_region_name":"7","id":"rs146360987","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513587,"source":"dbSNP","strand":1,"feature_type":"variation","end":140513587,"alleles":["G","A","T"]},{"seq_region_name":"7","id":"rs1795664593","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513587,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GAGA","GA"],"end":140513590},{"strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140513590,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513590,"source":"dbSNP","seq_region_name":"7","id":"rs1049959357","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1343515047","feature_type":"variation","strand":1,"end":140513594,"alleles":["CTCT","CT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513591},{"clinical_significance":[],"id":"rs1380114188","seq_region_name":"7","feature_type":"variation","strand":1,"end":140513592,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513592},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140513595,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513595,"clinical_significance":[],"id":"rs1335884677","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795664730","clinical_significance":[],"end":140513597,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140513597,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140513599,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140513599,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1391736446"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513600,"feature_type":"variation","strand":1,"alleles":["AAAAAAAAAAAA","AAAAAAAAA","AAAAAAAAAA","AAAAAAAAAAA","AAAAAAAAAAAAA"],"end":140513611,"clinical_significance":[],"seq_region_name":"7","id":"rs934902331"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513607,"source":"dbSNP","strand":1,"feature_type":"variation","end":140513607,"alleles":["A","C","T"],"id":"rs1222725029","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795664903","clinical_significance":[],"alleles":["A","G"],"end":140513609,"strand":1,"feature_type":"variation","start":140513609,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["T","C"],"end":140513617,"strand":1,"feature_type":"variation","start":140513617,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795664930","clinical_significance":[]},{"seq_region_name":"7","id":"rs1057286880","clinical_significance":[],"start":140513620,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140513620,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"start":140513622,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140513622,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795664988","clinical_significance":[]},{"id":"rs1795665017","seq_region_name":"7","clinical_significance":[],"alleles":["A","G"],"end":140513625,"strand":1,"feature_type":"variation","start":140513625,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140513626,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140513626,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1330160064","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795665079","alleles":["T","C"],"end":140513627,"feature_type":"variation","strand":1,"source":"dbSNP","start":140513627,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513628,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140513628,"clinical_significance":[],"seq_region_name":"7","id":"rs1795665106"},{"seq_region_name":"7","id":"rs1795665142","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513630,"source":"dbSNP","strand":1,"feature_type":"variation","end":140513630,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1241442023","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513631,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140513631},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513632,"feature_type":"variation","strand":1,"end":140513632,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795665224"},{"feature_type":"variation","strand":1,"end":140513633,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513633,"clinical_significance":[],"id":"rs1443054947","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795665290","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513635,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140513635},{"seq_region_name":"7","id":"rs1585528740","clinical_significance":[],"start":140513638,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140513638,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1259128578","seq_region_name":"7","source":"dbSNP","start":140513639,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140513639,"feature_type":"variation","strand":1},{"id":"rs1795665386","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513642,"source":"dbSNP","strand":1,"feature_type":"variation","end":140513642,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130432548","source":"dbSNP","start":140513644,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140513644,"alleles":["A","G","T"],"feature_type":"variation","strand":1},{"id":"rs2130432552","seq_region_name":"7","clinical_significance":[],"start":140513645,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140513645,"strand":1,"feature_type":"variation"},{"alleles":["TCATTTCAT","TCAT"],"end":140513653,"strand":1,"feature_type":"variation","start":140513645,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795665416","clinical_significance":[]},{"clinical_significance":[],"id":"rs2130432555","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140513646,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513646},{"clinical_significance":[],"id":"rs1384825490","seq_region_name":"7","end":140513647,"alleles":["A","C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140513647,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795665501","clinical_significance":[],"alleles":["T","C"],"end":140513648,"strand":1,"feature_type":"variation","start":140513648,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140513653,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140513653,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs896158984","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140513659,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513659,"clinical_significance":[],"seq_region_name":"7","id":"rs1585528749"},{"seq_region_name":"7","id":"rs1795665611","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513663,"source":"dbSNP","strand":1,"feature_type":"variation","end":140513663,"alleles":["A","G"]},{"strand":1,"feature_type":"variation","alleles":["GCTTTTTTTTTTTTT","-"],"end":140513682,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513668,"source":"dbSNP","seq_region_name":"7","id":"rs1795665640","clinical_significance":[]},{"clinical_significance":[],"id":"rs1585528754","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513669,"feature_type":"variation","strand":1,"alleles":["-","A","ATT","ATTTT","T","TT","TTTT"],"end":140513668},{"seq_region_name":"7","id":"rs1339285282","clinical_significance":[],"start":140513669,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","T"],"end":140513669,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["C","-"],"end":140513669,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513669,"source":"dbSNP","seq_region_name":"7","id":"rs1795665772","clinical_significance":[]},{"source":"dbSNP","start":140513670,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140513670,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1159376004","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs71173207","feature_type":"variation","strand":1,"alleles":["TTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTT","TTTTTTTTTTTTT","TTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT"],"end":140513695,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513670},{"id":"rs1795666099","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140513673,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513673,"source":"dbSNP"},{"start":140513674,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140513674,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795666130","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795666155","clinical_significance":[],"alleles":["T","C"],"end":140513676,"strand":1,"feature_type":"variation","start":140513676,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1455484968","feature_type":"variation","strand":1,"alleles":["-","C"],"end":140513680,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513681},{"source":"dbSNP","start":140513681,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140513681,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795666198"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130432633","source":"dbSNP","start":140513685,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140513685,"feature_type":"variation","strand":1},{"end":140513686,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140513686,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795666227","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795666261","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["TTTTTTTTG","-"],"end":140513696,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513688,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs762813388","source":"dbSNP","start":140513695,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TGAGATGAATCCT","T"],"end":140513707,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513696,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140513696,"seq_region_name":"7","id":"rs1452470496","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513696,"feature_type":"variation","strand":1,"alleles":["G","-"],"end":140513696,"clinical_significance":[],"id":"rs1485589426","seq_region_name":"7"},{"source":"dbSNP","start":140513697,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140513697,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1271712932","seq_region_name":"7"},{"alleles":["G","T"],"end":140513698,"feature_type":"variation","strand":1,"source":"dbSNP","start":140513698,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1481072145"},{"start":140513699,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G","T"],"end":140513699,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1489996976","clinical_significance":[]},{"clinical_significance":[],"id":"rs1585528782","seq_region_name":"7","end":140513700,"alleles":["T","TTTTT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140513700,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1199198383","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513701,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140513701},{"clinical_significance":[],"seq_region_name":"7","id":"rs1271652840","source":"dbSNP","start":140513703,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140513703,"alleles":["A","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs2130432677","clinical_significance":[],"alleles":["T","A"],"end":140513707,"strand":1,"feature_type":"variation","start":140513707,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1795666583","seq_region_name":"7","source":"dbSNP","start":140513708,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140513708,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1585528785","clinical_significance":[],"alleles":["A","C","T"],"end":140513709,"strand":1,"feature_type":"variation","start":140513709,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140513712,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140513712,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795666617","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513716,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","-"],"end":140513716,"id":"rs1252985633","seq_region_name":"7","clinical_significance":[]},{"end":140513716,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140513716,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1489656051"},{"strand":1,"feature_type":"variation","end":140513719,"alleles":["CGCC","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513716,"source":"dbSNP","seq_region_name":"7","id":"rs1197830988","clinical_significance":[]},{"source":"dbSNP","start":140513717,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140513717,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs564169751"},{"seq_region_name":"7","id":"rs1563109743","clinical_significance":[],"alleles":["CC","-"],"end":140513719,"strand":1,"feature_type":"variation","start":140513718,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs957859615","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513719,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140513719},{"source":"dbSNP","start":140513720,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140513720,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1352388671","seq_region_name":"7"},{"start":140513729,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140513729,"alleles":["T","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs989321844","clinical_significance":[]},{"start":140513729,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TGTAATG","TG"],"end":140513735,"strand":1,"feature_type":"variation","id":"rs1258786141","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1238037663","end":140513730,"alleles":["G","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140513730,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1421192935","clinical_significance":[],"strand":1,"feature_type":"variation","end":140513734,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513734,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513738,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140513738,"clinical_significance":[],"seq_region_name":"7","id":"rs1795666965"},{"end":140513740,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140513740,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795666988"},{"feature_type":"variation","strand":1,"end":140513743,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513743,"clinical_significance":[],"id":"rs2130432730","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1023812805","source":"dbSNP","start":140513745,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140513745,"alleles":["C","G"],"feature_type":"variation","strand":1},{"alleles":["A","C"],"end":140513747,"strand":1,"feature_type":"variation","start":140513747,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1585528805","seq_region_name":"7","clinical_significance":[]},{"start":140513748,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140513748,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs139729689","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795667113","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513749,"feature_type":"variation","strand":1,"end":140513749,"alleles":["C","T"]},{"end":140513751,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","start":140513751,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1344985999","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795667161","source":"dbSNP","start":140513754,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140513754,"alleles":["A","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1319045455","clinical_significance":[],"end":140513756,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140513756,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs995377133","clinical_significance":[],"start":140513758,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140513758,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1795667222","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513764,"feature_type":"variation","strand":1,"end":140513764,"alleles":["C","T"]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140513765,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513765,"clinical_significance":[],"id":"rs1026799380","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513768,"feature_type":"variation","strand":1,"end":140513768,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795667260"},{"clinical_significance":[],"id":"rs966634496","seq_region_name":"7","source":"dbSNP","start":140513770,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140513770,"feature_type":"variation","strand":1},{"alleles":["C","G","T"],"end":140513775,"feature_type":"variation","strand":1,"source":"dbSNP","start":140513775,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs753815481","seq_region_name":"7"},{"end":140513782,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140513782,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1207814303","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795667427","feature_type":"variation","strand":1,"end":140513785,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513785},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140513795,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513795,"clinical_significance":[],"seq_region_name":"7","id":"rs1795667465"},{"feature_type":"variation","strand":1,"end":140513796,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513796,"clinical_significance":[],"id":"rs528764495","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513797,"feature_type":"variation","strand":1,"end":140513797,"alleles":["C","G"],"clinical_significance":[],"id":"rs1795667517","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1363677233","end":140513801,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140513801,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["G","A","C"],"end":140513802,"strand":1,"feature_type":"variation","start":140513802,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1019490318","clinical_significance":[]},{"seq_region_name":"7","id":"rs928654933","clinical_significance":[],"start":140513807,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140513807,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"start":140513809,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140513809,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795667665","clinical_significance":[]},{"alleles":["C","T"],"end":140513817,"feature_type":"variation","strand":1,"source":"dbSNP","start":140513817,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795667699"},{"source":"dbSNP","start":140513818,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G","T"],"end":140513818,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs7790410"},{"seq_region_name":"7","id":"rs1245692076","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513819,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140513819},{"id":"rs1795667926","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140513825,"strand":1,"feature_type":"variation","start":140513825,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs372899593","alleles":["G","A","C"],"end":140513826,"feature_type":"variation","strand":1,"source":"dbSNP","start":140513826,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1259263768","clinical_significance":[],"start":140513831,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140513831,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795668034","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513832,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140513832},{"clinical_significance":[],"seq_region_name":"7","id":"rs1204149741","feature_type":"variation","strand":1,"end":140513833,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513833},{"id":"rs1795668100","seq_region_name":"7","clinical_significance":[],"end":140513834,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140513834,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140513838,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140513838,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs915994590"},{"seq_region_name":"7","id":"rs1585528853","clinical_significance":[],"start":140513840,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140513840,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1264713764","clinical_significance":[],"end":140513843,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140513843,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1563109779","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513847,"feature_type":"variation","strand":1,"end":140513847,"alleles":["T","C"]},{"id":"rs1221667758","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140513849,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513849,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795668289","clinical_significance":[],"alleles":["A","G"],"end":140513851,"strand":1,"feature_type":"variation","start":140513851,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1795668322","seq_region_name":"7","source":"dbSNP","start":140513854,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140513854,"alleles":["T","C"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140513863,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513863,"clinical_significance":[],"seq_region_name":"7","id":"rs2130432891"},{"seq_region_name":"7","id":"rs1795668359","clinical_significance":[],"strand":1,"feature_type":"variation","end":140513866,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513866,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1305176086","clinical_significance":[],"alleles":["T","A"],"end":140513867,"strand":1,"feature_type":"variation","start":140513867,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs149855883","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140513873,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513873,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140513874,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513874,"clinical_significance":[],"seq_region_name":"7","id":"rs1795668470"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513877,"feature_type":"variation","strand":1,"end":140513877,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795668490"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513880,"feature_type":"variation","strand":1,"end":140513880,"alleles":["G","C"],"clinical_significance":[],"id":"rs1795668529","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795668562","alleles":["A","C"],"end":140513885,"feature_type":"variation","strand":1,"source":"dbSNP","start":140513885,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795668604","clinical_significance":[],"start":140513887,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140513887,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs947476558","alleles":["TGGCC","TGGCCTGGCC"],"end":140513896,"feature_type":"variation","strand":1,"source":"dbSNP","start":140513892,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140513893,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513893,"source":"dbSNP","seq_region_name":"7","id":"rs1795668659","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140513894,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513894,"source":"dbSNP","seq_region_name":"7","id":"rs978929905","clinical_significance":[]},{"id":"rs765177921","seq_region_name":"7","clinical_significance":[],"start":140513903,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140513903,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs113316595","clinical_significance":[],"alleles":["C","A","G"],"end":140513905,"strand":1,"feature_type":"variation","start":140513905,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1453566967","source":"dbSNP","start":140513907,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140513907,"alleles":["G","A"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140513909,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513909,"source":"dbSNP","id":"rs1585528884","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","C"],"end":140513911,"feature_type":"variation","strand":1,"source":"dbSNP","start":140513911,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1408775062"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140513912,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513912,"source":"dbSNP","seq_region_name":"7","id":"rs1585528888","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795668879","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513913,"feature_type":"variation","strand":1,"end":140513913,"alleles":["T","C"]},{"source":"dbSNP","start":140513922,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140513922,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1222382120"},{"clinical_significance":[],"id":"rs1057319321","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513925,"feature_type":"variation","strand":1,"end":140513925,"alleles":["T","G"]},{"feature_type":"variation","strand":1,"end":140513926,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513926,"clinical_significance":[],"seq_region_name":"7","id":"rs1795668972"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795669002","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513931,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140513931},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513933,"source":"dbSNP","strand":1,"feature_type":"variation","end":140513933,"alleles":["T","G"],"seq_region_name":"7","id":"rs1469776017","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795669054","alleles":["C","A"],"end":140513934,"feature_type":"variation","strand":1,"source":"dbSNP","start":140513934,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1420820951","seq_region_name":"7","source":"dbSNP","start":140513934,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140513935,"alleles":["CC","CCC"],"feature_type":"variation","strand":1},{"id":"rs1795669131","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140513937,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513937,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs908808039","end":140513952,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140513952,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795669188","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513955,"feature_type":"variation","strand":1,"alleles":["AGTGCT","-"],"end":140513960},{"seq_region_name":"7","id":"rs1170101355","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513957,"source":"dbSNP","strand":1,"feature_type":"variation","end":140513957,"alleles":["T","C","G"]},{"clinical_significance":[],"id":"rs940301051","seq_region_name":"7","feature_type":"variation","strand":1,"end":140513958,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513958},{"clinical_significance":[],"seq_region_name":"7","id":"rs896034910","end":140513962,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140513962,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1370780124","source":"dbSNP","start":140513963,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140513963,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795669389","clinical_significance":[],"alleles":["T","C"],"end":140513966,"strand":1,"feature_type":"variation","start":140513966,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130433006","alleles":["A","G"],"end":140513967,"feature_type":"variation","strand":1,"source":"dbSNP","start":140513967,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs949106439","seq_region_name":"7","alleles":["G","A"],"end":140513973,"feature_type":"variation","strand":1,"source":"dbSNP","start":140513973,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1461483455","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513975,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140513975},{"feature_type":"variation","strand":1,"end":140513976,"alleles":["A","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513976,"clinical_significance":[],"id":"rs1041663857","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs190619326","end":140513986,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140513986,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1249440391","alleles":["A","G"],"end":140513989,"feature_type":"variation","strand":1,"source":"dbSNP","start":140513989,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795669574","clinical_significance":[],"end":140513991,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140513991,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140513992,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140513992,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1216214584","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585528927","feature_type":"variation","strand":1,"end":140513997,"alleles":["A","C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140513997},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140513999,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140513999,"seq_region_name":"7","id":"rs995241247","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1423996798","end":140514000,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140514000,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1795669719","seq_region_name":"7","source":"dbSNP","start":140514003,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140514003,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514008,"feature_type":"variation","strand":1,"end":140514008,"alleles":["G","A"],"clinical_significance":[],"id":"rs10257237","seq_region_name":"7"},{"end":140514009,"alleles":["A","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140514009,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs180906759"},{"alleles":["G","A"],"end":140514012,"feature_type":"variation","strand":1,"source":"dbSNP","start":140514012,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1385225426"},{"seq_region_name":"7","id":"rs1795669859","clinical_significance":[],"end":140514015,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140514015,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140514024,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140514024,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1313438487","clinical_significance":[]},{"start":140514027,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140514027,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795669919","clinical_significance":[]},{"alleles":["T","C"],"end":140514028,"strand":1,"feature_type":"variation","start":140514028,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795669950","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140514029,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514029,"source":"dbSNP","id":"rs1795669975","seq_region_name":"7","clinical_significance":[]},{"end":140514030,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140514030,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1452401088","clinical_significance":[]},{"seq_region_name":"7","id":"rs1048142933","clinical_significance":[],"start":140514035,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140514035,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1331467010","clinical_significance":[],"end":140514036,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140514036,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514039,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140514039,"seq_region_name":"7","id":"rs886956383","clinical_significance":[]},{"source":"dbSNP","start":140514043,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140514043,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795670085"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140514045,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514045,"source":"dbSNP","id":"rs758087463","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1423395965","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140514046,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514046},{"clinical_significance":[],"seq_region_name":"7","id":"rs893548710","source":"dbSNP","start":140514053,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140514053,"alleles":["G","A"],"feature_type":"variation","strand":1},{"start":140514055,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140514055,"strand":1,"feature_type":"variation","id":"rs2130433109","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140514056,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514056,"clinical_significance":[],"id":"rs1356169738","seq_region_name":"7"},{"end":140514057,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140514057,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1386680155","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140514058,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514058,"clinical_significance":[],"seq_region_name":"7","id":"rs1795670271"},{"source":"dbSNP","start":140514059,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140514059,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1011180669","seq_region_name":"7"},{"end":140514063,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140514063,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795670306"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130433124","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140514066,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514066},{"seq_region_name":"7","id":"rs1472360670","clinical_significance":[],"alleles":["T","C","G"],"end":140514068,"strand":1,"feature_type":"variation","start":140514068,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140514070,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514070,"clinical_significance":[],"seq_region_name":"7","id":"rs1585528970"},{"end":140514071,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140514071,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1233175365"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1020804777","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514076,"feature_type":"variation","strand":1,"end":140514076,"alleles":["G","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs771407324","alleles":["GGG","GG"],"end":140514078,"feature_type":"variation","strand":1,"source":"dbSNP","start":140514076,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs4726876","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140514080,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514080},{"strand":1,"feature_type":"variation","alleles":["GGA","-"],"end":140514083,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514081,"source":"dbSNP","seq_region_name":"7","id":"rs1563109825","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130433157","alleles":["G","A"],"end":140514082,"feature_type":"variation","strand":1,"source":"dbSNP","start":140514082,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140514083,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140514083,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs555076104","clinical_significance":[]},{"alleles":["A","G"],"end":140514085,"feature_type":"variation","strand":1,"source":"dbSNP","start":140514085,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795670770","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140514091,"alleles":["TTG","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514089,"source":"dbSNP","seq_region_name":"7","id":"rs1453652845","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514097,"feature_type":"variation","strand":1,"end":140514097,"alleles":["A","T"],"clinical_significance":[],"id":"rs1003472552","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1223291452","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140514099,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514099},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514100,"source":"dbSNP","strand":1,"feature_type":"variation","end":140514100,"alleles":["G","A"],"seq_region_name":"7","id":"rs1795670873","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514101,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TTTTT","TTTT"],"end":140514105,"seq_region_name":"7","id":"rs1795670902","clinical_significance":[]},{"source":"dbSNP","start":140514103,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140514103,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795670934","seq_region_name":"7"},{"alleles":["T","C"],"end":140514107,"strand":1,"feature_type":"variation","start":140514107,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1361620114","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514108,"source":"dbSNP","strand":1,"feature_type":"variation","end":140514108,"alleles":["C","A"],"seq_region_name":"7","id":"rs1795670995","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514109,"feature_type":"variation","strand":1,"end":140514109,"alleles":["C","T"],"clinical_significance":[],"id":"rs573631494","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514110,"feature_type":"variation","strand":1,"end":140514110,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs960071524"},{"clinical_significance":[],"id":"rs1374528690","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140514111,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514111},{"seq_region_name":"7","id":"rs1795671093","clinical_significance":[],"strand":1,"feature_type":"variation","end":140514112,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514112,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514121,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140514121,"id":"rs1281620595","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140514124,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140514124,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1245288140"},{"source":"dbSNP","start":140514125,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140514125,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs534593170"},{"start":140514126,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140514126,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs916023718","clinical_significance":[]},{"clinical_significance":[],"id":"rs956086033","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514131,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140514131},{"seq_region_name":"7","id":"rs1424774873","clinical_significance":[],"end":140514132,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140514132,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140514137,"alleles":["TTTTTT","TTTTT"],"strand":1,"feature_type":"variation","start":140514132,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs371786245","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1202912094","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514139,"feature_type":"variation","strand":1,"alleles":["A","C","T"],"end":140514139},{"feature_type":"variation","strand":1,"end":140514139,"alleles":["-","TT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514140,"clinical_significance":[],"seq_region_name":"7","id":"rs1795671392"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585529041","feature_type":"variation","strand":1,"end":140514140,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514140},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514140,"feature_type":"variation","strand":1,"alleles":["CT","CTCT"],"end":140514141,"clinical_significance":[],"id":"rs1366852625","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1554455630","clinical_significance":[],"alleles":["-","CTT"],"end":140514140,"strand":1,"feature_type":"variation","start":140514141,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140514141,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514141,"source":"dbSNP","seq_region_name":"7","id":"rs1795671480","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795671495","alleles":["T","TCTT"],"end":140514141,"feature_type":"variation","strand":1,"source":"dbSNP","start":140514141,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs764771234","clinical_significance":[],"strand":1,"feature_type":"variation","end":140514157,"alleles":["TTTTTTTTTTTTTTTTT","TTTTTTTT","TTTTTTTTTTTTT","TTTTTTTTTTTTTT","TTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514141,"source":"dbSNP"},{"end":140514142,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140514142,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1251099290"},{"start":140514142,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140514142,"alleles":["T","TCT"],"strand":1,"feature_type":"variation","id":"rs1795671674","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1490861616","alleles":["TT","TTTTCTT"],"end":140514157,"feature_type":"variation","strand":1,"source":"dbSNP","start":140514156,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs76074335","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140514157,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514157,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs59293189","feature_type":"variation","strand":1,"alleles":["-","TC"],"end":140514157,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514158},{"clinical_significance":[],"seq_region_name":"7","id":"rs75402617","end":140514158,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140514158,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1221182301","clinical_significance":[],"start":140514158,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","-"],"end":140514158,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514158,"feature_type":"variation","strand":1,"alleles":["CA","-"],"end":140514159,"clinical_significance":[],"id":"rs1767189053","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795671866","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514158,"feature_type":"variation","strand":1,"alleles":["CAA","-"],"end":140514160},{"clinical_significance":[],"seq_region_name":"7","id":"rs866919477","feature_type":"variation","strand":1,"alleles":["A","C","G","T"],"end":140514159,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514159},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514160,"source":"dbSNP","strand":1,"feature_type":"variation","end":140514160,"alleles":["A","C","G","T"],"seq_region_name":"7","id":"rs757915136","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140514162,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514162,"clinical_significance":[],"seq_region_name":"7","id":"rs1328857003"},{"seq_region_name":"7","id":"rs777194841","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514163,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C","T"],"end":140514163},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130433260","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514165,"feature_type":"variation","strand":1,"end":140514165,"alleles":["G","T"]},{"source":"dbSNP","start":140514168,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140514168,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs553340742","seq_region_name":"7"},{"alleles":["C","T"],"end":140514175,"feature_type":"variation","strand":1,"source":"dbSNP","start":140514175,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs746739163","seq_region_name":"7"},{"seq_region_name":"7","id":"rs952805948","clinical_significance":[],"end":140514176,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140514176,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1435398715","clinical_significance":[],"alleles":["C","T"],"end":140514185,"strand":1,"feature_type":"variation","start":140514185,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1345393848","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514186,"feature_type":"variation","strand":1,"end":140514186,"alleles":["C","G"]},{"end":140514188,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140514188,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1585529081","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1188591526","clinical_significance":[],"alleles":["T","C","G"],"end":140514195,"strand":1,"feature_type":"variation","start":140514195,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795672228","clinical_significance":[],"start":140514196,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140514196,"strand":1,"feature_type":"variation"},{"start":140514197,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140514197,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795672248","clinical_significance":[]},{"source":"dbSNP","start":140514199,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140514199,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs984586493"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140514200,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514200,"source":"dbSNP","id":"rs1795672307","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514203,"source":"dbSNP","strand":1,"feature_type":"variation","end":140514203,"alleles":["T","C"],"id":"rs1585529088","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514214,"feature_type":"variation","strand":1,"end":140514214,"alleles":["A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs577984386"},{"seq_region_name":"7","id":"rs1585529094","clinical_significance":[],"alleles":["A","C"],"end":140514222,"strand":1,"feature_type":"variation","start":140514222,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140514227,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140514227,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs544899374"},{"feature_type":"variation","strand":1,"end":140514230,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514230,"clinical_significance":[],"seq_region_name":"7","id":"rs1041321324"},{"seq_region_name":"7","id":"rs563463730","clinical_significance":[],"end":140514232,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140514232,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs992947829","clinical_significance":[],"alleles":["T","C"],"end":140514234,"strand":1,"feature_type":"variation","start":140514234,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140514235,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140514235,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795672557"},{"clinical_significance":[],"seq_region_name":"7","id":"rs922845326","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514238,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140514238},{"seq_region_name":"7","id":"rs1585529112","clinical_significance":[],"start":140514240,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G","T"],"end":140514240,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140514241,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514241,"clinical_significance":[],"id":"rs1470800779","seq_region_name":"7"},{"start":140514242,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140514242,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1486346536","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514246,"feature_type":"variation","strand":1,"end":140514246,"alleles":["G","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795672682"},{"id":"rs1244083996","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514251,"source":"dbSNP","strand":1,"feature_type":"variation","end":140514251,"alleles":["G","A","C"]},{"end":140514252,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140514252,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130433334","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs932335859","end":140514254,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140514254,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1464734610","clinical_significance":[],"strand":1,"feature_type":"variation","end":140514258,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514258,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1338979339","feature_type":"variation","strand":1,"end":140514260,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514260},{"strand":1,"feature_type":"variation","end":140514265,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514265,"source":"dbSNP","id":"rs1264083486","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140514267,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514267,"source":"dbSNP","seq_region_name":"7","id":"rs1795672854","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795672880","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140514274,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514274},{"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140514276,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514276,"clinical_significance":[],"id":"rs2130433350","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1563109878","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514278,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140514278},{"alleles":["C","A"],"end":140514281,"feature_type":"variation","strand":1,"source":"dbSNP","start":140514281,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795672937"},{"clinical_significance":[],"seq_region_name":"7","id":"rs186337192","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514282,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140514282},{"end":140514283,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140514283,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs948979261","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1298610995","feature_type":"variation","strand":1,"end":140514285,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514285},{"seq_region_name":"7","id":"rs1795673490","clinical_significance":[],"alleles":["T","G"],"end":140514289,"strand":1,"feature_type":"variation","start":140514289,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1795673517","seq_region_name":"7","source":"dbSNP","start":140514290,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140514290,"alleles":["T","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795673555","source":"dbSNP","start":140514291,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140514291,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795673581","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514291,"feature_type":"variation","strand":1,"end":140514292,"alleles":["AA","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs893455031","end":140514296,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140514296,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","T"],"end":140514299,"feature_type":"variation","strand":1,"source":"dbSNP","start":140514299,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1270811479","seq_region_name":"7"},{"end":140514301,"alleles":["A","G","T"],"strand":1,"feature_type":"variation","start":140514301,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs748748332","clinical_significance":[]},{"seq_region_name":"7","id":"rs567563914","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514305,"source":"dbSNP","strand":1,"feature_type":"variation","end":140514305,"alleles":["T","G"]},{"alleles":["G","C"],"end":140514313,"feature_type":"variation","strand":1,"source":"dbSNP","start":140514313,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1290269868"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1295415783","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514314,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140514314},{"source":"dbSNP","start":140514315,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140514315,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1042498259"},{"seq_region_name":"7","id":"rs112265153","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514319,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140514319},{"clinical_significance":[],"id":"rs1003787030","seq_region_name":"7","source":"dbSNP","start":140514321,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140514321,"alleles":["G","T"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140514323,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140514323,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs778149943"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140514324,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514324,"clinical_significance":[],"seq_region_name":"7","id":"rs1795673946"},{"alleles":["C","T"],"end":140514327,"strand":1,"feature_type":"variation","start":140514327,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1585529152","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140514328,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514328,"clinical_significance":[],"id":"rs1585529154","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140514329,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514329,"clinical_significance":[],"seq_region_name":"7","id":"rs1795674032"},{"id":"rs1427092877","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514330,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140514330},{"alleles":["G","C"],"end":140514331,"feature_type":"variation","strand":1,"source":"dbSNP","start":140514331,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs745618485"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514336,"source":"dbSNP","strand":1,"feature_type":"variation","end":140514336,"alleles":["T","C"],"seq_region_name":"7","id":"rs1260893396","clinical_significance":[]},{"start":140514338,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140514338,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795674142","clinical_significance":[]},{"alleles":["G","C"],"end":140514339,"feature_type":"variation","strand":1,"source":"dbSNP","start":140514339,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1421661183"},{"source":"dbSNP","start":140514339,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140514349,"alleles":["GATGTGTGTTT","GATGTGTGTTTTTTTGAGACAGATGTGTGTTT"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1035088392"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1185014248","alleles":["A","G"],"end":140514340,"feature_type":"variation","strand":1,"source":"dbSNP","start":140514340,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1048183410","seq_region_name":"7","source":"dbSNP","start":140514341,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140514341,"feature_type":"variation","strand":1},{"id":"rs749685369","seq_region_name":"7","clinical_significance":[],"end":140514342,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140514342,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514351,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140514351,"clinical_significance":[],"seq_region_name":"7","id":"rs886851650"},{"end":140514356,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140514356,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1004090099","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514359,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140514359,"seq_region_name":"7","id":"rs1460221067","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795674414","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514360,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140514360},{"seq_region_name":"7","id":"rs1795674440","clinical_significance":[],"strand":1,"feature_type":"variation","end":140514361,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514361,"source":"dbSNP"},{"seq_region_name":"7","id":"rs895051487","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514364,"source":"dbSNP","strand":1,"feature_type":"variation","end":140514364,"alleles":["G","T"]},{"feature_type":"variation","strand":1,"end":140514366,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514366,"clinical_significance":[],"seq_region_name":"7","id":"rs1012892152"},{"id":"rs1243342735","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514371,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140514371},{"feature_type":"variation","strand":1,"end":140514373,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514373,"clinical_significance":[],"seq_region_name":"7","id":"rs1795674521"},{"seq_region_name":"7","id":"rs1255952202","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514380,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140514380},{"clinical_significance":[],"seq_region_name":"7","id":"rs372398768","source":"dbSNP","start":140514381,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140514381,"alleles":["C","A","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795674689","clinical_significance":[],"end":140514384,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140514384,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs561044480","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514389,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140514389},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514390,"feature_type":"variation","strand":1,"end":140514390,"alleles":["G","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs984228806"},{"seq_region_name":"7","id":"rs1225804559","clinical_significance":[],"strand":1,"feature_type":"variation","end":140514396,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514396,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1425737491","end":140514397,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140514397,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1454400788","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140514399,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514399},{"start":140514402,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140514402,"alleles":["T","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795674948","clinical_significance":[]},{"id":"rs1399751166","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["TTTT","TT","TTT"],"end":140514411,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514408,"source":"dbSNP"},{"end":140514416,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140514416,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs996789923","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1028635079","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514421,"feature_type":"variation","strand":1,"end":140514421,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs1795675086","clinical_significance":[],"strand":1,"feature_type":"variation","end":140514422,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514422,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs374718774","source":"dbSNP","start":140514423,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140514423,"alleles":["G","A","T"],"feature_type":"variation","strand":1},{"start":140514425,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140514425,"alleles":["A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585529203","clinical_significance":[]},{"id":"rs1795675189","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140514428,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514428,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514431,"source":"dbSNP","strand":1,"feature_type":"variation","end":140514431,"alleles":["G","A"],"id":"rs1356414561","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1168423226","source":"dbSNP","start":140514433,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140514433,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514436,"source":"dbSNP","strand":1,"feature_type":"variation","end":140514436,"alleles":["G","C"],"seq_region_name":"7","id":"rs1795675267","clinical_significance":[]},{"id":"rs1469476101","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140514437,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514437,"source":"dbSNP"},{"seq_region_name":"7","id":"rs968693389","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140514442,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514442,"source":"dbSNP"},{"source":"dbSNP","start":140514443,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140514443,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1000117927"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795675411","source":"dbSNP","start":140514444,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140514444,"alleles":["G","T"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514452,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140514452,"clinical_significance":[],"id":"rs1795675437","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1443170601","clinical_significance":[],"strand":1,"feature_type":"variation","end":140514453,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514453,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140514459,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514459,"clinical_significance":[],"seq_region_name":"7","id":"rs1795675495"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514461,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140514461,"seq_region_name":"7","id":"rs1428636935","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795675547","alleles":["C","T"],"end":140514466,"feature_type":"variation","strand":1,"source":"dbSNP","start":140514466,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140514468,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514468,"source":"dbSNP","seq_region_name":"7","id":"rs1288832662","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795675613","feature_type":"variation","strand":1,"end":140514474,"alleles":["CCC","CC"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514472},{"feature_type":"variation","strand":1,"end":140514474,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514474,"clinical_significance":[],"seq_region_name":"7","id":"rs1795675641"},{"alleles":["C","T"],"end":140514476,"strand":1,"feature_type":"variation","start":140514476,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795675671","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795675710","source":"dbSNP","start":140514477,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140514477,"alleles":["T","G"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140514478,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514478,"source":"dbSNP","seq_region_name":"7","id":"rs2130433520","clinical_significance":[]},{"seq_region_name":"7","id":"rs528506653","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514479,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140514479},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514481,"feature_type":"variation","strand":1,"end":140514481,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs961606104"},{"source":"dbSNP","start":140514482,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140514482,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs759465372"},{"seq_region_name":"7","id":"rs1795675850","clinical_significance":[],"alleles":["A","T"],"end":140514483,"strand":1,"feature_type":"variation","start":140514483,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140514484,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140514484,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795675870"},{"end":140514490,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140514490,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795675895","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs546574026","source":"dbSNP","start":140514493,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C","T"],"end":140514493,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795675969","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140514496,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514496},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585529226","source":"dbSNP","start":140514504,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140514504,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140514507,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514507,"clinical_significance":[],"seq_region_name":"7","id":"rs1795676036"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514508,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140514508,"id":"rs1585529229","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs922872603","clinical_significance":[],"end":140514509,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140514509,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1322476834","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140514513,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514513,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1202376555","alleles":["C","G"],"end":140514514,"feature_type":"variation","strand":1,"source":"dbSNP","start":140514514,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs770271474","source":"dbSNP","start":140514517,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140514518,"alleles":["CC","C"],"feature_type":"variation","strand":1},{"start":140514518,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140514518,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs932907150","clinical_significance":[]},{"seq_region_name":"7","id":"rs1292096281","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514519,"source":"dbSNP","strand":1,"feature_type":"variation","end":140514519,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1247636114","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514520,"source":"dbSNP","strand":1,"feature_type":"variation","end":140514520,"alleles":["T","C"]},{"strand":1,"feature_type":"variation","end":140514525,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514525,"source":"dbSNP","seq_region_name":"7","id":"rs985681646","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs917408839","feature_type":"variation","strand":1,"end":140514526,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514526},{"start":140514528,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140514528,"strand":1,"feature_type":"variation","id":"rs1375403123","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140514529,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514529,"clinical_significance":[],"seq_region_name":"7","id":"rs1795676360"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514530,"feature_type":"variation","strand":1,"end":140514530,"alleles":["T","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585529253"},{"start":140514531,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140514531,"alleles":["G","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795676420","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140514533,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514533,"source":"dbSNP","seq_region_name":"7","id":"rs1795676462","clinical_significance":[]},{"alleles":["C","G"],"end":140514538,"feature_type":"variation","strand":1,"source":"dbSNP","start":140514538,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795676483","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514539,"source":"dbSNP","strand":1,"feature_type":"variation","end":140514542,"alleles":["TTTT","TTTTT"],"seq_region_name":"7","id":"rs1795676509","clinical_significance":[]},{"start":140514543,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","G"],"end":140514543,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585529257","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs914920555","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514544,"feature_type":"variation","strand":1,"end":140514544,"alleles":["A","C"]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140514547,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514547,"clinical_significance":[],"seq_region_name":"7","id":"rs980395966"},{"alleles":["C","T"],"end":140514548,"feature_type":"variation","strand":1,"source":"dbSNP","start":140514548,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1366199967","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140514549,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514549,"clinical_significance":[],"seq_region_name":"7","id":"rs1795676605"},{"clinical_significance":[],"id":"rs1214397579","seq_region_name":"7","end":140514553,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140514553,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140514561,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514561,"source":"dbSNP","seq_region_name":"7","id":"rs1456569314","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514566,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140514566,"clinical_significance":[],"seq_region_name":"7","id":"rs920804852"},{"alleles":["T","C"],"end":140514570,"strand":1,"feature_type":"variation","start":140514570,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs565264313","clinical_significance":[]},{"seq_region_name":"7","id":"rs946337332","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514571,"source":"dbSNP","strand":1,"feature_type":"variation","end":140514571,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1490811000","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514577,"feature_type":"variation","strand":1,"end":140514577,"alleles":["T","C"]},{"alleles":["AAAA","A"],"end":140514581,"strand":1,"feature_type":"variation","start":140514578,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1182043315","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1197096057","source":"dbSNP","start":140514583,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140514588,"alleles":["AAAAAA","AAAAAAA"],"feature_type":"variation","strand":1},{"alleles":["C","T"],"end":140514591,"feature_type":"variation","strand":1,"source":"dbSNP","start":140514591,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795676913"},{"source":"dbSNP","start":140514592,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140514592,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1042180521"},{"seq_region_name":"7","id":"rs1795676961","clinical_significance":[],"alleles":["G","A","C"],"end":140514594,"strand":1,"feature_type":"variation","start":140514594,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["GG","G"],"end":140514595,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514594,"source":"dbSNP","seq_region_name":"7","id":"rs1795677001","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563109939","feature_type":"variation","strand":1,"end":140514595,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514595},{"seq_region_name":"7","id":"rs1795677039","clinical_significance":[],"end":140514598,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140514598,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1224331849","clinical_significance":[],"start":140514601,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140514601,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"id":"rs1795677099","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514602,"source":"dbSNP","strand":1,"feature_type":"variation","end":140514602,"alleles":["G","A","C","T"]},{"strand":1,"feature_type":"variation","end":140514604,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514604,"source":"dbSNP","seq_region_name":"7","id":"rs117277573","clinical_significance":[]},{"source":"dbSNP","start":140514605,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140514605,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795677161","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs983787548","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514609,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140514609},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795677217","source":"dbSNP","start":140514611,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140514611,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140514613,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A","C"],"end":140514613,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs902255267","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130433625","source":"dbSNP","start":140514615,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140514615,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514624,"feature_type":"variation","strand":1,"end":140514624,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795677282"},{"end":140514628,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140514628,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795677308"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514630,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140514630,"clinical_significance":[],"seq_region_name":"7","id":"rs1795677340"},{"clinical_significance":[],"id":"rs1795677363","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140514631,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514631},{"strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140514633,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514633,"source":"dbSNP","seq_region_name":"7","id":"rs939229800","clinical_significance":[]},{"alleles":["GGG","GGGG"],"end":140514636,"strand":1,"feature_type":"variation","start":140514634,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs34364380","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs532635785","source":"dbSNP","start":140514635,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140514635,"alleles":["G","A"],"feature_type":"variation","strand":1},{"id":"rs1056206443","seq_region_name":"7","clinical_significance":[],"start":140514636,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140514636,"strand":1,"feature_type":"variation"},{"alleles":["G","A"],"end":140514638,"strand":1,"feature_type":"variation","start":140514638,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs894956568","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1041164981","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514639,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140514639},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585529326","source":"dbSNP","start":140514643,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140514643,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1409077000","source":"dbSNP","start":140514644,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140514644,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs901026096","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140514646,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514646,"source":"dbSNP"},{"seq_region_name":"7","id":"rs2130433649","clinical_significance":[],"end":140514647,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140514647,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1305026782","seq_region_name":"7","end":140514649,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140514649,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140514653,"alleles":["A","C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514653,"clinical_significance":[],"seq_region_name":"7","id":"rs1385347971"},{"seq_region_name":"7","id":"rs550960026","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140514654,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514654,"source":"dbSNP"},{"end":140514663,"alleles":["C","A","G","T"],"strand":1,"feature_type":"variation","start":140514663,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1159311220","clinical_significance":[]},{"end":140514669,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140514669,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585529341"},{"seq_region_name":"7","id":"rs550907784","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514675,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140514675},{"clinical_significance":[],"seq_region_name":"7","id":"rs1027494312","source":"dbSNP","start":140514682,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140514682,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs776414718","clinical_significance":[],"start":140514684,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140514684,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"end":140514691,"alleles":["T","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140514691,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs11773778"},{"seq_region_name":"7","id":"rs2130433690","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514692,"source":"dbSNP","strand":1,"feature_type":"variation","end":140514692,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795678129","source":"dbSNP","start":140514693,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140514693,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140514693,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140514694,"alleles":["GG","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1200335549"},{"alleles":["T","C","G"],"end":140514695,"strand":1,"feature_type":"variation","start":140514695,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1449564438","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1158452638","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140514698,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514698},{"source":"dbSNP","start":140514699,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140514699,"alleles":["T","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795678230"},{"source":"dbSNP","start":140514700,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140514700,"alleles":["T","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1205284813","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514702,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140514702,"clinical_significance":[],"seq_region_name":"7","id":"rs113850576"},{"seq_region_name":"7","id":"rs113997421","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514703,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140514703},{"alleles":["C","T"],"end":140514712,"strand":1,"feature_type":"variation","start":140514712,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1301748657","clinical_significance":[]},{"alleles":["C","A"],"end":140514713,"strand":1,"feature_type":"variation","start":140514713,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795678412","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130433729","clinical_significance":[],"start":140514719,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140514719,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140514720,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514720,"source":"dbSNP","seq_region_name":"7","id":"rs1795678443","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140514721,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514721,"source":"dbSNP","id":"rs1585529375","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140514726,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514726,"source":"dbSNP","id":"rs2130433732","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514727,"feature_type":"variation","strand":1,"end":140514727,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795678484"},{"feature_type":"variation","strand":1,"end":140514728,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514728,"clinical_significance":[],"id":"rs567355280","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs11773781","feature_type":"variation","strand":1,"alleles":["T","A","C","G"],"end":140514729,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514729},{"seq_region_name":"7","id":"rs1443300862","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140514730,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514730,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140514732,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514732,"clinical_significance":[],"id":"rs1795678683","seq_region_name":"7"},{"source":"dbSNP","start":140514733,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140514733,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795678705","seq_region_name":"7"},{"source":"dbSNP","start":140514734,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140514734,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1585529394","seq_region_name":"7"},{"source":"dbSNP","start":140514741,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140514741,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1330549986"},{"end":140514742,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140514742,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795678902"},{"source":"dbSNP","start":140514743,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140514743,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1319236829"},{"strand":1,"feature_type":"variation","alleles":["ACGA","ACGAACGA"],"end":140514747,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514744,"source":"dbSNP","seq_region_name":"7","id":"rs1795678952","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140514745,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514745,"source":"dbSNP","seq_region_name":"7","id":"rs1386984222","clinical_significance":[]},{"seq_region_name":"7","id":"rs1384083058","clinical_significance":[],"alleles":["-","TT"],"end":140514745,"strand":1,"feature_type":"variation","start":140514746,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs954160787","feature_type":"variation","strand":1,"end":140514746,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514746},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795679089","alleles":["A","G"],"end":140514747,"feature_type":"variation","strand":1,"source":"dbSNP","start":140514747,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140514748,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140514748,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1024785426","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140514749,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514749,"clinical_significance":[],"id":"rs867669402","seq_region_name":"7"},{"alleles":["A","G"],"end":140514752,"strand":1,"feature_type":"variation","start":140514752,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795679157","seq_region_name":"7","clinical_significance":[]},{"start":140514754,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140514754,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795679178","clinical_significance":[]},{"seq_region_name":"7","id":"rs1171286487","clinical_significance":[],"strand":1,"feature_type":"variation","end":140514768,"alleles":["AGCTCAAGACCAGC","AGC"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514755,"source":"dbSNP"},{"source":"dbSNP","start":140514756,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140514756,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795679216"},{"alleles":["C","T"],"end":140514757,"strand":1,"feature_type":"variation","start":140514757,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs915478244","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs552979179","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514762,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140514762},{"id":"rs1585529413","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514763,"source":"dbSNP","strand":1,"feature_type":"variation","end":140514763,"alleles":["A","C"]},{"strand":1,"feature_type":"variation","end":140514769,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514769,"source":"dbSNP","seq_region_name":"7","id":"rs1795679323","clinical_significance":[]},{"start":140514770,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140514770,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795679345","clinical_significance":[]},{"id":"rs578010545","seq_region_name":"7","clinical_significance":[],"alleles":["C","A"],"end":140514773,"strand":1,"feature_type":"variation","start":140514773,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1795679387","seq_region_name":"7","clinical_significance":[],"start":140514775,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140514775,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs980671331","seq_region_name":"7","end":140514777,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140514777,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140514779,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514779,"source":"dbSNP","seq_region_name":"7","id":"rs1563109975","clinical_significance":[]},{"start":140514787,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140514787,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1027950126","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795679490","clinical_significance":[],"start":140514788,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140514788,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1585529423","clinical_significance":[],"start":140514789,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","T"],"end":140514789,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514789,"feature_type":"variation","strand":1,"end":140514790,"alleles":["CT","-"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585529425"},{"alleles":["G","A","C"],"end":140514791,"feature_type":"variation","strand":1,"source":"dbSNP","start":140514791,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1290855856","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514792,"source":"dbSNP","strand":1,"feature_type":"variation","end":140514792,"alleles":["T","C"],"id":"rs191583675","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795679652","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514803,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140514803},{"seq_region_name":"7","id":"rs1795679679","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514804,"source":"dbSNP","strand":1,"feature_type":"variation","end":140514804,"alleles":["A","G"]},{"id":"rs1438211476","seq_region_name":"7","clinical_significance":[],"alleles":["A","ACAAA"],"end":140514806,"strand":1,"feature_type":"variation","start":140514806,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1461561759","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514807,"feature_type":"variation","strand":1,"end":140514807,"alleles":["A","G"]},{"strand":1,"feature_type":"variation","end":140514810,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514810,"source":"dbSNP","seq_region_name":"7","id":"rs1795679767","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795679796","seq_region_name":"7","source":"dbSNP","start":140514811,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140514811,"alleles":["T","C"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514813,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140514813,"seq_region_name":"7","id":"rs983818541","clinical_significance":[]},{"end":140514815,"alleles":["T","C","G"],"strand":1,"feature_type":"variation","start":140514815,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs923735850","clinical_significance":[]},{"alleles":["G","A"],"end":140514816,"strand":1,"feature_type":"variation","start":140514816,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1344422759","clinical_significance":[]},{"alleles":["A","G"],"end":140514820,"strand":1,"feature_type":"variation","start":140514820,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs908221315","seq_region_name":"7","clinical_significance":[]},{"id":"rs879492431","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514827,"source":"dbSNP","strand":1,"feature_type":"variation","end":140514827,"alleles":["C","T"]},{"id":"rs1056111511","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514828,"source":"dbSNP","strand":1,"feature_type":"variation","end":140514828,"alleles":["A","G"]},{"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140514829,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514829,"clinical_significance":[],"id":"rs1297391488","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs922311390","feature_type":"variation","strand":1,"end":140514830,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514830},{"clinical_significance":[],"seq_region_name":"7","id":"rs894989236","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140514831,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514831},{"feature_type":"variation","strand":1,"end":140514832,"alleles":["G","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514832,"clinical_significance":[],"seq_region_name":"7","id":"rs947850884"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1049009987","alleles":["C","T"],"end":140514833,"feature_type":"variation","strand":1,"source":"dbSNP","start":140514833,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795680178","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514834,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140514834},{"seq_region_name":"7","id":"rs887683052","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514836,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140514836},{"seq_region_name":"7","id":"rs1795680224","clinical_significance":[],"start":140514838,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140514838,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"start":140514841,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140514841,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795680247","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795680260","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514842,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140514842},{"seq_region_name":"7","id":"rs1167956970","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514843,"source":"dbSNP","strand":1,"feature_type":"variation","end":140514843,"alleles":["T","C"]},{"id":"rs556881962","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140514851,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514851,"source":"dbSNP"},{"end":140514852,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140514852,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs575444492"},{"start":140514853,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140514853,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs542446129","clinical_significance":[]},{"id":"rs1795680877","seq_region_name":"7","clinical_significance":[],"alleles":["A","T"],"end":140514855,"strand":1,"feature_type":"variation","start":140514855,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1387959783","clinical_significance":[],"start":140514861,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140514861,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514863,"feature_type":"variation","strand":1,"end":140514863,"alleles":["G","A"],"clinical_significance":[],"id":"rs1795680927","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1037457779","seq_region_name":"7","source":"dbSNP","start":140514873,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140514873,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs141110034","clinical_significance":[],"start":140514874,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C"],"end":140514874,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs998279896","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514877,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140514877},{"alleles":["A","C","G"],"end":140514880,"strand":1,"feature_type":"variation","start":140514880,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs182825565","clinical_significance":[]},{"seq_region_name":"7","id":"rs1333688036","clinical_significance":[],"strand":1,"feature_type":"variation","end":140514883,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514883,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs540252873","source":"dbSNP","start":140514884,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140514884,"alleles":["G","A","C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795681172","source":"dbSNP","start":140514886,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140514886,"alleles":["G","A"],"feature_type":"variation","strand":1},{"alleles":["A","G"],"end":140514891,"strand":1,"feature_type":"variation","start":140514891,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1315239016","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795681213","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514893,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140514893},{"source":"dbSNP","start":140514895,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140514895,"alleles":["G","C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1384366503","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1795681269","seq_region_name":"7","source":"dbSNP","start":140514899,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140514899,"feature_type":"variation","strand":1},{"start":140514900,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140514900,"alleles":["A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795681303","clinical_significance":[]},{"seq_region_name":"7","id":"rs1246903130","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514905,"source":"dbSNP","strand":1,"feature_type":"variation","end":140514905,"alleles":["G","C"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514907,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140514907,"clinical_significance":[],"seq_region_name":"7","id":"rs1243078638"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1282785298","source":"dbSNP","start":140514908,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140514908,"alleles":["G","A"],"feature_type":"variation","strand":1},{"id":"rs1314317065","seq_region_name":"7","clinical_significance":[],"start":140514910,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140514910,"strand":1,"feature_type":"variation"},{"start":140514913,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C","G","T"],"end":140514913,"strand":1,"feature_type":"variation","id":"rs1339972560","seq_region_name":"7","clinical_significance":[]},{"start":140514914,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140514914,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1336846653","clinical_significance":[]},{"start":140514915,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140514915,"alleles":["C","A","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs377390297","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514916,"feature_type":"variation","strand":1,"end":140514916,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs149866110"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1014629309","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514917,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140514917},{"clinical_significance":[],"seq_region_name":"7","id":"rs1436348944","feature_type":"variation","strand":1,"end":140514922,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514922},{"seq_region_name":"7","id":"rs1424893332","clinical_significance":[],"end":140514924,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140514924,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140514926,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514926,"source":"dbSNP","id":"rs1795681761","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1415783075","end":140514927,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140514927,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514928,"source":"dbSNP","strand":1,"feature_type":"variation","end":140514928,"alleles":["T","C"],"seq_region_name":"7","id":"rs1198266413","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514930,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140514930,"seq_region_name":"7","id":"rs1795681842","clinical_significance":[]},{"source":"dbSNP","start":140514931,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140514931,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795681913"},{"seq_region_name":"7","id":"rs1472455706","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514932,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140514932},{"clinical_significance":[],"seq_region_name":"7","id":"rs1233410738","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514934,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140514934},{"clinical_significance":[],"seq_region_name":"7","id":"rs1243906983","feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140514937,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514937},{"clinical_significance":[],"seq_region_name":"7","id":"rs1482118195","alleles":["G","A"],"end":140514938,"feature_type":"variation","strand":1,"source":"dbSNP","start":140514938,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795682030","alleles":["GACAGACTGA","GA"],"end":140514947,"feature_type":"variation","strand":1,"source":"dbSNP","start":140514938,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514940,"feature_type":"variation","strand":1,"end":140514940,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585529522"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795682070","source":"dbSNP","start":140514943,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140514943,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795682100","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514946,"source":"dbSNP","strand":1,"feature_type":"variation","end":140514946,"alleles":["G","T"]},{"seq_region_name":"7","id":"rs1585529525","clinical_significance":[],"start":140514949,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140514949,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795682157","alleles":["C","G"],"end":140514950,"feature_type":"variation","strand":1,"source":"dbSNP","start":140514950,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140514952,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514952,"source":"dbSNP","seq_region_name":"7","id":"rs1251153208","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs773161030","feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140514954,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514954},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795682263","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514955,"feature_type":"variation","strand":1,"end":140514958,"alleles":["TCTC","TC"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1323695699","source":"dbSNP","start":140514956,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140514956,"alleles":["C","A","G","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795682310","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514957,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["-","A"],"end":140514956},{"end":140514957,"alleles":["T","-"],"strand":1,"feature_type":"variation","start":140514957,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795682333","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514957,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140514957,"clinical_significance":[],"id":"rs2130433992","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1181805595","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514958,"source":"dbSNP","strand":1,"feature_type":"variation","end":140514957,"alleles":["-","A","AA"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs867000347","end":140514958,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140514958,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1288230308","clinical_significance":[],"start":140514958,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","-"],"end":140514958,"strand":1,"feature_type":"variation"},{"start":140514958,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140514958,"alleles":["C","CC"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795682418","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140514959,"alleles":["CA","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514958,"source":"dbSNP","id":"rs1491185565","seq_region_name":"7","clinical_significance":[]},{"alleles":["CAA","-"],"end":140514960,"strand":1,"feature_type":"variation","start":140514958,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1351794308","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563110066","source":"dbSNP","start":140514958,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["CAAA","-"],"end":140514961,"feature_type":"variation","strand":1},{"alleles":["AAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAA","AAAAAAAAAAAAAA","AAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAA"],"end":140514978,"feature_type":"variation","strand":1,"source":"dbSNP","start":140514959,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1305946375"},{"seq_region_name":"7","id":"rs1491409790","clinical_significance":[],"start":140514960,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140514959,"alleles":["-","G"],"strand":1,"feature_type":"variation"},{"id":"rs1795682708","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514960,"source":"dbSNP","strand":1,"feature_type":"variation","end":140514960,"alleles":["A","C","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs113417791","end":140514961,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140514961,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514962,"feature_type":"variation","strand":1,"alleles":["-","G"],"end":140514961,"clinical_significance":[],"seq_region_name":"7","id":"rs1161302138"},{"seq_region_name":"7","id":"rs113073497","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140514962,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514962,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140514963,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514963,"clinical_significance":[],"seq_region_name":"7","id":"rs1444766827"},{"strand":1,"feature_type":"variation","end":140514965,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514965,"source":"dbSNP","seq_region_name":"7","id":"rs1795682854","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2033697519","feature_type":"variation","strand":1,"end":140515030,"alleles":["AAAAAAAAAAAAAAGAACAGCCCTGGCAACATAGTGAGATCCCATCTCTACCAAAAAAAAAAAAAA","AAAAAAAAAAAAAA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514965},{"id":"rs1200205893","seq_region_name":"7","clinical_significance":[],"start":140514966,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["-","G"],"end":140514965,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1795682905","clinical_significance":[],"start":140514967,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140514967,"alleles":["A","AGA"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["-","G","T"],"end":140514967,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514968,"clinical_significance":[],"id":"rs1489476750","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795682969","clinical_significance":[],"strand":1,"feature_type":"variation","end":140514968,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514968,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795682995","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514971,"feature_type":"variation","strand":1,"end":140514970,"alleles":["-","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1245228734","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514971,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140514971},{"source":"dbSNP","start":140514973,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140514973,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795683061","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514974,"source":"dbSNP","strand":1,"feature_type":"variation","end":140514974,"alleles":["A","C"],"seq_region_name":"7","id":"rs1795683082","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795683106","feature_type":"variation","strand":1,"end":140514974,"alleles":["-","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514975},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514975,"source":"dbSNP","strand":1,"feature_type":"variation","end":140514975,"alleles":["A","G"],"seq_region_name":"7","id":"rs1409681173","clinical_significance":[]},{"id":"rs1795683154","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140514981,"alleles":["AAAAGAA","AA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514975,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795683174","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514976,"source":"dbSNP","strand":1,"feature_type":"variation","end":140514975,"alleles":["-","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795683195","alleles":["A","G"],"end":140514976,"feature_type":"variation","strand":1,"source":"dbSNP","start":140514976,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["A","G"],"end":140514977,"feature_type":"variation","strand":1,"source":"dbSNP","start":140514977,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795683217"},{"seq_region_name":"7","id":"rs1447950160","clinical_significance":[],"strand":1,"feature_type":"variation","end":140514981,"alleles":["AAGAA","AA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514977,"source":"dbSNP"},{"id":"rs1795683269","seq_region_name":"7","clinical_significance":[],"start":140514978,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140514977,"alleles":["-","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1287220552","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514978,"feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140514978},{"seq_region_name":"7","id":"rs1491247039","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514978,"source":"dbSNP","strand":1,"feature_type":"variation","end":140514980,"alleles":["AGA","A"]},{"alleles":["-","AT"],"end":140514978,"feature_type":"variation","strand":1,"source":"dbSNP","start":140514979,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1491211032"},{"start":140514979,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140514979,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs980154014","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140514979,"alleles":["G","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514979,"source":"dbSNP","seq_region_name":"7","id":"rs1260177946","clinical_significance":[]},{"seq_region_name":"7","id":"rs1554455749","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514979,"source":"dbSNP","strand":1,"feature_type":"variation","end":140514979,"alleles":["G","GG"]},{"seq_region_name":"7","id":"rs1407777255","clinical_significance":[],"end":140514982,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140514982,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140514983,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140514983,"alleles":["A","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795683520","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514984,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140514984,"id":"rs1585529596","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1435236967","feature_type":"variation","strand":1,"end":140514986,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514986},{"strand":1,"feature_type":"variation","end":140514991,"alleles":["CTGGC","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514987,"source":"dbSNP","seq_region_name":"7","id":"rs2130434081","clinical_significance":[]},{"source":"dbSNP","start":140514988,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140514988,"alleles":["T","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585529600"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585529602","feature_type":"variation","strand":1,"end":140514989,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514989},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514990,"feature_type":"variation","strand":1,"end":140514990,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1449898492"},{"seq_region_name":"7","id":"rs1322260982","clinical_significance":[],"strand":1,"feature_type":"variation","end":140514991,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514991,"source":"dbSNP"},{"seq_region_name":"7","id":"rs2130434096","clinical_significance":[],"alleles":["AA","AAAAAAAAAAAAAAAAA"],"end":140514993,"strand":1,"feature_type":"variation","start":140514992,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140514994,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140514994,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585529607","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514995,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140514995,"id":"rs1387844598","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140514995,"feature_type":"variation","strand":1,"end":140514995,"alleles":["A","AAA"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130434105"},{"alleles":["T","A"],"end":140514996,"strand":1,"feature_type":"variation","start":140514996,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585529611","clinical_significance":[]},{"seq_region_name":"7","id":"rs1177016928","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140514997,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514997,"source":"dbSNP"},{"seq_region_name":"7","id":"rs2130434113","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["GTG","-"],"end":140515000,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140514998,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1585529614","seq_region_name":"7","source":"dbSNP","start":140514999,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140514999,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1434982073","feature_type":"variation","strand":1,"end":140515002,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515002},{"seq_region_name":"7","id":"rs2130434121","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515002,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GATCCCATCT","-"],"end":140515011},{"start":140515004,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140515004,"strand":1,"feature_type":"variation","id":"rs1585529617","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795683919","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515006,"feature_type":"variation","strand":1,"end":140515006,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1335459091","end":140515007,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140515007,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1795683979","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140515009,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515009,"source":"dbSNP"},{"id":"rs2130434136","seq_region_name":"7","clinical_significance":[],"start":140515010,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140515010,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1795684006","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140515011,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515011,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs372043733","feature_type":"variation","strand":1,"end":140515012,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515012},{"strand":1,"feature_type":"variation","end":140515013,"alleles":["T","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515013,"source":"dbSNP","seq_region_name":"7","id":"rs1274432752","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs905942550","feature_type":"variation","strand":1,"end":140515014,"alleles":["A","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515014},{"source":"dbSNP","start":140515015,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140515015,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1459929843"},{"strand":1,"feature_type":"variation","alleles":["-","A","AAA","AAAA","AAAAA","AAAAAA"],"end":140515015,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515016,"source":"dbSNP","seq_region_name":"7","id":"rs1264341009","clinical_significance":[]},{"seq_region_name":"7","id":"rs866392185","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515016,"source":"dbSNP","strand":1,"feature_type":"variation","end":140515016,"alleles":["C","A"]},{"alleles":["-","CAAAAA","GAAAA"],"end":140515016,"feature_type":"variation","strand":1,"source":"dbSNP","start":140515017,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795684208"},{"seq_region_name":"7","id":"rs1229506130","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140515017,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515017,"source":"dbSNP"},{"source":"dbSNP","start":140515017,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140515034,"alleles":["AAAAAAAAAAAAAAAAAA","AAAAAAAAA","AAAAAAAAAAA","AAAAAAAAAAAAAA","AAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAA"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs773310260"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1449247258","alleles":["A","C"],"end":140515021,"feature_type":"variation","strand":1,"source":"dbSNP","start":140515021,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140515027,"alleles":["AAAAA","AAAAAGAAAAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140515023,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795684415"},{"id":"rs1795684438","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140515024,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515024,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1244068542","source":"dbSNP","start":140515025,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140515025,"alleles":["A","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795684486","clinical_significance":[],"start":140515025,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AAAAA","AAAAAGAAAAA"],"end":140515029,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795684515","alleles":["A","T"],"end":140515028,"feature_type":"variation","strand":1,"source":"dbSNP","start":140515028,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515030,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140515030,"id":"rs1795684525","seq_region_name":"7","clinical_significance":[]},{"start":140515033,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140515033,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795684546","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140515034,"alleles":["-","AAAAAT","AAAAATT","AAAAT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515035,"source":"dbSNP","seq_region_name":"7","id":"rs1795684569","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515035,"feature_type":"variation","strand":1,"end":140515035,"alleles":["T","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1243554297"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1446274867","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515036,"feature_type":"variation","strand":1,"end":140515036,"alleles":["T","A","C"]},{"strand":1,"feature_type":"variation","alleles":["C","A","G","T"],"end":140515037,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515037,"source":"dbSNP","seq_region_name":"7","id":"rs1190718683","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795684675","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140515038,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515038},{"seq_region_name":"7","id":"rs1264014461","clinical_significance":[],"strand":1,"feature_type":"variation","end":140515039,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515039,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140515044,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515044,"clinical_significance":[],"id":"rs2130434212","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1585529662","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140515045,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515045,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515046,"feature_type":"variation","strand":1,"end":140515046,"alleles":["A","C"],"clinical_significance":[],"id":"rs1585529664","seq_region_name":"7"},{"start":140515047,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140515047,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585529668","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795684782","seq_region_name":"7","source":"dbSNP","start":140515048,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140515048,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795684809","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515050,"source":"dbSNP","strand":1,"feature_type":"variation","end":140515050,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1184171926","clinical_significance":[],"alleles":["A","T"],"end":140515053,"strand":1,"feature_type":"variation","start":140515053,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795684850","source":"dbSNP","start":140515054,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140515054,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140515056,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515056,"clinical_significance":[],"seq_region_name":"7","id":"rs1795684867"},{"source":"dbSNP","start":140515058,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","G"],"end":140515058,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585529671"},{"seq_region_name":"7","id":"rs1462799140","clinical_significance":[],"alleles":["G","T"],"end":140515065,"strand":1,"feature_type":"variation","start":140515065,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs2130434248","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140515066,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515066,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795684937","clinical_significance":[],"end":140515067,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140515067,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795684955","source":"dbSNP","start":140515068,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TGAC","TGACTGAC"],"end":140515071,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs113788769","clinical_significance":[],"start":140515069,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140515069,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1795685035","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515071,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140515071},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515074,"source":"dbSNP","strand":1,"feature_type":"variation","end":140515074,"alleles":["C","G","T"],"id":"rs1795685052","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795685077","source":"dbSNP","start":140515076,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140515076,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140515079,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515079,"clinical_significance":[],"seq_region_name":"7","id":"rs2130434265"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515080,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","G"],"end":140515080,"seq_region_name":"7","id":"rs1027812703","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140515082,"alleles":["CCC","CC"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515080,"clinical_significance":[],"id":"rs1795685118","seq_region_name":"7"},{"start":140515083,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140515083,"strand":1,"feature_type":"variation","id":"rs1795685136","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130434275","clinical_significance":[],"alleles":["GGA","-"],"end":140515086,"strand":1,"feature_type":"variation","start":140515084,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["G","A","T"],"end":140515088,"feature_type":"variation","strand":1,"source":"dbSNP","start":140515088,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs952163618"},{"id":"rs2130434277","seq_region_name":"7","clinical_significance":[],"start":140515089,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140515089,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140515091,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515091,"clinical_significance":[],"seq_region_name":"7","id":"rs2130434280"},{"seq_region_name":"7","id":"rs1795685175","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515092,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140515092},{"clinical_significance":[],"seq_region_name":"7","id":"rs563036383","feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140515094,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515094},{"clinical_significance":[],"id":"rs1795685253","seq_region_name":"7","alleles":["C","G"],"end":140515095,"feature_type":"variation","strand":1,"source":"dbSNP","start":140515095,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140515096,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140515096,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1276335789","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs4726878","end":140515097,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140515097,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs112044653","clinical_significance":[],"start":140515098,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140515098,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515103,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","T"],"end":140515103,"id":"rs1795685380","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515104,"feature_type":"variation","strand":1,"end":140515104,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1313152510"},{"id":"rs1795685428","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140515105,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515105,"source":"dbSNP"},{"alleles":["A","G","T"],"end":140515107,"strand":1,"feature_type":"variation","start":140515107,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1585529695","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1397758650","source":"dbSNP","start":140515109,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C","G","T"],"end":140515109,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795685497","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515112,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140515112},{"seq_region_name":"7","id":"rs1371802994","clinical_significance":[],"start":140515112,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["CC","C","CCC"],"end":140515113,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140515113,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["-","ATTTT","T","TT","TTT"],"end":140515112,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1477709657"},{"seq_region_name":"7","id":"rs1462676408","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140515113,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515113,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795685599","source":"dbSNP","start":140515114,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140515113,"alleles":["-","CTT"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515114,"feature_type":"variation","strand":1,"end":140515114,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1265864811"},{"clinical_significance":[],"id":"rs1795685653","seq_region_name":"7","alleles":["TT","TTCTTT"],"end":140515115,"feature_type":"variation","strand":1,"source":"dbSNP","start":140515114,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["TTTTTTTTTTTTTTTTTTT","TTTTTTTTT","TTTTTTTTTTT","TTTTTTTTTTTT","TTTTTTTTTTTTTT","TTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTT"],"end":140515132,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515114,"clinical_significance":[],"seq_region_name":"7","id":"rs34254245"},{"seq_region_name":"7","id":"rs1177568329","clinical_significance":[],"start":140515115,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140515115,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1431032236","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140515118,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515118},{"strand":1,"feature_type":"variation","alleles":["TT","TTCTT"],"end":140515119,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515118,"source":"dbSNP","seq_region_name":"7","id":"rs1795685921","clinical_significance":[]},{"clinical_significance":[],"id":"rs1246751985","seq_region_name":"7","source":"dbSNP","start":140515119,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140515119,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795685949","clinical_significance":[],"alleles":["T","A","C"],"end":140515121,"strand":1,"feature_type":"variation","start":140515121,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["T","TAT"],"end":140515128,"strand":1,"feature_type":"variation","start":140515128,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795685976","clinical_significance":[]},{"end":140515129,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140515129,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1319663989"},{"clinical_significance":[],"id":"rs76434422","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515131,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140515131},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515131,"source":"dbSNP","strand":1,"feature_type":"variation","end":140515133,"alleles":["TTG","-"],"id":"rs1795686019","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1311928774","clinical_significance":[],"strand":1,"feature_type":"variation","end":140515132,"alleles":["T","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515132,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1795686031","seq_region_name":"7","source":"dbSNP","start":140515132,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TG","-"],"end":140515133,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795686079","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515132,"feature_type":"variation","strand":1,"alleles":["TGA","-"],"end":140515134},{"feature_type":"variation","strand":1,"alleles":["-","TTTTTTA"],"end":140515132,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515133,"clinical_significance":[],"id":"rs1795686085","seq_region_name":"7"},{"start":140515133,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140515133,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs79137340","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","GG"],"end":140515133,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515133,"clinical_significance":[],"seq_region_name":"7","id":"rs1228870234"},{"source":"dbSNP","start":140515133,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","-"],"end":140515133,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1399022555"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795686175","alleles":["GAG","-"],"end":140515135,"feature_type":"variation","strand":1,"source":"dbSNP","start":140515133,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["GAGA","GA"],"end":140515136,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515133,"clinical_significance":[],"id":"rs1795686189","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515133,"feature_type":"variation","strand":1,"end":140515139,"alleles":["GAGACAG","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795686227"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1403911083","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515134,"feature_type":"variation","strand":1,"end":140515134,"alleles":["A","G","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795686263","feature_type":"variation","strand":1,"end":140515134,"alleles":["A","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515134},{"start":140515135,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140515135,"alleles":["G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1171549281","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515136,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140515136,"clinical_significance":[],"seq_region_name":"7","id":"rs1409495034"},{"start":140515137,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140515137,"alleles":["C","A","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795686306","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515138,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140515138,"clinical_significance":[],"seq_region_name":"7","id":"rs1795686339"},{"alleles":["G","A"],"end":140515139,"strand":1,"feature_type":"variation","start":140515139,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1385070633","clinical_significance":[]},{"id":"rs1295466761","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140515140,"alleles":["T","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515140,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1383349346","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140515141,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515141,"source":"dbSNP"},{"alleles":["C","A","T"],"end":140515145,"strand":1,"feature_type":"variation","start":140515145,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795686405","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515146,"source":"dbSNP","strand":1,"feature_type":"variation","end":140515146,"alleles":["A","C","G"],"seq_region_name":"7","id":"rs1585529751","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140515148,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515148,"source":"dbSNP","seq_region_name":"7","id":"rs1368196099","clinical_significance":[]},{"source":"dbSNP","start":140515153,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140515153,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1316171954"},{"id":"rs1795686476","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515154,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140515154},{"clinical_significance":[],"seq_region_name":"7","id":"rs111275489","source":"dbSNP","start":140515155,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","G","T"],"end":140515155,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515156,"feature_type":"variation","strand":1,"end":140515156,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1482416217"},{"source":"dbSNP","start":140515157,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140515157,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs375747949","seq_region_name":"7"},{"id":"rs201361475","seq_region_name":"7","clinical_significance":[],"end":140515158,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140515158,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140515160,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515160,"clinical_significance":[],"seq_region_name":"7","id":"rs1264625039"},{"end":140515161,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140515161,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795686649","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140515163,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515163,"source":"dbSNP","id":"rs2130434441","seq_region_name":"7","clinical_significance":[]},{"start":140515164,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140515164,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1209354162","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140515165,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515165,"clinical_significance":[],"seq_region_name":"7","id":"rs1331098359"},{"strand":1,"feature_type":"variation","end":140515167,"alleles":["T","A","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515167,"source":"dbSNP","id":"rs976817234","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1303695291","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515168,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140515168},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515170,"source":"dbSNP","strand":1,"feature_type":"variation","end":140515170,"alleles":["A","G"],"id":"rs1795686747","seq_region_name":"7","clinical_significance":[]},{"end":140515171,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140515171,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1385290111","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795686789","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515172,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["-","CG"],"end":140515171},{"feature_type":"variation","strand":1,"end":140515172,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515172,"clinical_significance":[],"seq_region_name":"7","id":"rs1795686804"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515173,"feature_type":"variation","strand":1,"end":140515173,"alleles":["G","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795686829"},{"seq_region_name":"7","id":"rs546628049","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","G","T"],"end":140515175,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515175,"source":"dbSNP"},{"id":"rs571216088","seq_region_name":"7","clinical_significance":[],"start":140515176,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140515176,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1795686962","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515178,"source":"dbSNP","strand":1,"feature_type":"variation","end":140515178,"alleles":["G","A"]},{"source":"dbSNP","start":140515184,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140515184,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1351531070"},{"seq_region_name":"7","id":"rs1159027095","clinical_significance":[],"strand":1,"feature_type":"variation","end":140515188,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515188,"source":"dbSNP"},{"end":140515190,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140515190,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795687028"},{"seq_region_name":"7","id":"rs1795687050","clinical_significance":[],"strand":1,"feature_type":"variation","end":140515193,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515193,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1469189356","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140515194,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515194},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515195,"source":"dbSNP","strand":1,"feature_type":"variation","end":140515195,"alleles":["A","C","G","T"],"seq_region_name":"7","id":"rs1377644610","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515197,"source":"dbSNP","strand":1,"feature_type":"variation","end":140515197,"alleles":["C","T"],"id":"rs538253714","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140515199,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140515199,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1200627124"},{"clinical_significance":[],"seq_region_name":"7","id":"rs142056370","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515201,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140515201},{"source":"dbSNP","start":140515209,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140515209,"alleles":["A","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs73492312"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515214,"source":"dbSNP","strand":1,"feature_type":"variation","end":140515214,"alleles":["A","G"],"seq_region_name":"7","id":"rs1795687293","clinical_significance":[]},{"clinical_significance":[],"id":"rs2130434494","seq_region_name":"7","alleles":["A","G"],"end":140515215,"feature_type":"variation","strand":1,"source":"dbSNP","start":140515215,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795687306","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515216,"feature_type":"variation","strand":1,"end":140515216,"alleles":["G","A"]},{"feature_type":"variation","strand":1,"end":140515217,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515217,"clinical_significance":[],"id":"rs1795687321","seq_region_name":"7"},{"seq_region_name":"7","id":"rs954235039","clinical_significance":[],"start":140515218,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140515218,"strand":1,"feature_type":"variation"},{"start":140515219,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140515219,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795687358","clinical_significance":[]},{"seq_region_name":"7","id":"rs1266169524","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515221,"source":"dbSNP","strand":1,"feature_type":"variation","end":140515221,"alleles":["C","A","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515228,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140515228,"seq_region_name":"7","id":"rs777096326","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140515229,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515229,"source":"dbSNP","seq_region_name":"7","id":"rs536473965","clinical_significance":[]},{"seq_region_name":"7","id":"rs1257825328","clinical_significance":[],"start":140515234,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140515234,"strand":1,"feature_type":"variation"},{"id":"rs1795687476","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515241,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140515241},{"seq_region_name":"7","id":"rs1479629703","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140515243,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515243,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1231384056","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140515244,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515244,"source":"dbSNP"},{"source":"dbSNP","start":140515246,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140515246,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs925799545"},{"seq_region_name":"7","id":"rs1298549704","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140515249,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515249,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515251,"feature_type":"variation","strand":1,"end":140515251,"alleles":["A","AA"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795687569"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515255,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140515255,"clinical_significance":[],"seq_region_name":"7","id":"rs935811646"},{"strand":1,"feature_type":"variation","end":140515258,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515258,"source":"dbSNP","seq_region_name":"7","id":"rs968689045","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1363390006","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515259,"feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140515259},{"clinical_significance":[],"id":"rs1174922438","seq_region_name":"7","feature_type":"variation","strand":1,"end":140515263,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515263},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515264,"feature_type":"variation","strand":1,"end":140515264,"alleles":["G","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1052966768"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795687699","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515265,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140515265},{"id":"rs1795687712","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515266,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140515266},{"source":"dbSNP","start":140515267,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140515267,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795687728"},{"end":140515269,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140515269,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795687744"},{"source":"dbSNP","start":140515271,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140515271,"alleles":["C","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795687754"},{"strand":1,"feature_type":"variation","end":140515272,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515272,"source":"dbSNP","seq_region_name":"7","id":"rs1795687771","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515277,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140515277,"clinical_significance":[],"seq_region_name":"7","id":"rs1795687789"},{"seq_region_name":"7","id":"rs978342005","clinical_significance":[],"alleles":["A","G"],"end":140515281,"strand":1,"feature_type":"variation","start":140515281,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140515282,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140515286,"alleles":["TTTTT","TTTT"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1173790982","seq_region_name":"7"},{"clinical_significance":[],"id":"rs923612589","seq_region_name":"7","source":"dbSNP","start":140515283,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140515283,"alleles":["T","G"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515287,"source":"dbSNP","strand":1,"feature_type":"variation","end":140515287,"alleles":["G","A"],"seq_region_name":"7","id":"rs1795687874","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515290,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140515290,"clinical_significance":[],"seq_region_name":"7","id":"rs1156282623"},{"id":"rs1464276159","seq_region_name":"7","clinical_significance":[],"end":140515294,"alleles":["TTTTT","TTT"],"strand":1,"feature_type":"variation","start":140515290,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1359896228","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515293,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140515293},{"end":140515295,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140515295,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795687966"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140515297,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515297,"source":"dbSNP","seq_region_name":"7","id":"rs950120966","clinical_significance":[]},{"end":140515299,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140515299,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795688000","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515307,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140515307,"clinical_significance":[],"seq_region_name":"7","id":"rs960327627"},{"source":"dbSNP","start":140515314,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140515314,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795688036"},{"alleles":["A","C","G"],"end":140515315,"feature_type":"variation","strand":1,"source":"dbSNP","start":140515315,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs991871394"},{"clinical_significance":[],"id":"rs1795688147","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140515316,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515316},{"clinical_significance":[],"seq_region_name":"7","id":"rs1192459894","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515321,"feature_type":"variation","strand":1,"end":140515321,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs866585809","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140515325,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515325},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795688267","alleles":["T","C"],"end":140515328,"feature_type":"variation","strand":1,"source":"dbSNP","start":140515328,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs905977343","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140515329,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515329,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795688325","clinical_significance":[],"start":140515330,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140515330,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs916327970","clinical_significance":[],"strand":1,"feature_type":"variation","end":140515334,"alleles":["C","A","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515334,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs947924198","source":"dbSNP","start":140515335,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140515335,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795688464","source":"dbSNP","start":140515337,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140515337,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795688491","clinical_significance":[],"strand":1,"feature_type":"variation","end":140515338,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515338,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515339,"source":"dbSNP","strand":1,"feature_type":"variation","end":140515339,"alleles":["T","G"],"seq_region_name":"7","id":"rs1795688528","clinical_significance":[]},{"source":"dbSNP","start":140515344,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140515344,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1230818150"},{"strand":1,"feature_type":"variation","end":140515348,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515348,"source":"dbSNP","seq_region_name":"7","id":"rs1340562316","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1336552009","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140515353,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515353},{"id":"rs1297315432","seq_region_name":"7","clinical_significance":[],"end":140515358,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140515358,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140515359,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140515361,"alleles":["CCC","CC"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795688680"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515362,"feature_type":"variation","strand":1,"end":140515362,"alleles":["A","C","G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1049355660"},{"source":"dbSNP","start":140515363,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140515363,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795688765"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515364,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140515364,"seq_region_name":"7","id":"rs1795688802","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515366,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140515366,"seq_region_name":"7","id":"rs1049151786","clinical_significance":[]},{"end":140515369,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140515369,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795688904"},{"seq_region_name":"7","id":"rs1795688936","clinical_significance":[],"strand":1,"feature_type":"variation","end":140515370,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515370,"source":"dbSNP"},{"end":140515375,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140515375,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795688966","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795689000","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515376,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140515376},{"seq_region_name":"7","id":"rs887948623","clinical_significance":[],"strand":1,"feature_type":"variation","end":140515377,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515377,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140515378,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515378,"source":"dbSNP","seq_region_name":"7","id":"rs1005020615","clinical_significance":[]},{"source":"dbSNP","start":140515390,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140515390,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs909024022","seq_region_name":"7"},{"seq_region_name":"7","id":"rs940617352","clinical_significance":[],"strand":1,"feature_type":"variation","end":140515394,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515394,"source":"dbSNP"},{"source":"dbSNP","start":140515395,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140515395,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs759927939"},{"clinical_significance":[],"id":"rs1353695566","seq_region_name":"7","feature_type":"variation","strand":1,"end":140515396,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515396},{"alleles":["T","C"],"end":140515399,"strand":1,"feature_type":"variation","start":140515399,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs2130434679","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1223905295","feature_type":"variation","strand":1,"alleles":["TGTTTTGTTTTGTTTTG","TGTTTTGTTTTG","TGTTTTGTTTTGTTTTGTTTTG"],"end":140515415,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515399},{"seq_region_name":"7","id":"rs1795689309","clinical_significance":[],"alleles":["G","A"],"end":140515400,"strand":1,"feature_type":"variation","start":140515400,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1472974380","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140515411,"strand":1,"feature_type":"variation","start":140515411,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795689357","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515413,"feature_type":"variation","strand":1,"end":140515413,"alleles":["T","C"]},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140515415,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515415,"clinical_significance":[],"seq_region_name":"7","id":"rs1585529917"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515417,"source":"dbSNP","strand":1,"feature_type":"variation","end":140515417,"alleles":["A","G"],"id":"rs1795689390","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","G"],"end":140515418,"strand":1,"feature_type":"variation","start":140515418,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795689415","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["AGTCACTCAGGTTGCTC","AGTCACTCAGGTTGCTCAGTCACTCAGGTTGCTC"],"end":140515434,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515418,"source":"dbSNP","seq_region_name":"7","id":"rs1795689438","clinical_significance":[]},{"end":140515419,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140515419,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585529921","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515419,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GTCACTCAGGTTGCTCTGTCACTCAGGTTG","GTCACTCAGGTTGCTCTGTCACTCAGGTTGCTCTGTCACTCAGGTTG","GTCACTCAGGTTGCTCTGTCACTCAGGTTGCTCTGTCACTCAGGTTGCTCTGTCACTCAGGTTG"],"end":140515448,"seq_region_name":"7","id":"rs961165069","clinical_significance":[]},{"start":140515422,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140515422,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795689512","clinical_significance":[]},{"end":140515426,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140515426,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1294508005","clinical_significance":[]},{"alleles":["G","C"],"end":140515428,"strand":1,"feature_type":"variation","start":140515428,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1489971061","clinical_significance":[]},{"seq_region_name":"7","id":"rs1485395426","clinical_significance":[],"strand":1,"feature_type":"variation","end":140515430,"alleles":["T","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515430,"source":"dbSNP"},{"alleles":["T","C"],"end":140515435,"feature_type":"variation","strand":1,"source":"dbSNP","start":140515435,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795689591"},{"source":"dbSNP","start":140515437,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TCACTCA","TCACTCACTCA"],"end":140515443,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795689613"},{"end":140515438,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140515438,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs554314898","clinical_significance":[]},{"end":140515439,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140515439,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs138808596"},{"seq_region_name":"7","id":"rs985193319","clinical_significance":[],"start":140515440,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140515440,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515441,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140515441,"id":"rs1272806395","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515444,"source":"dbSNP","strand":1,"feature_type":"variation","end":140515444,"alleles":["G","C"],"seq_region_name":"7","id":"rs897162178","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515446,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140515446,"seq_region_name":"7","id":"rs754434498","clinical_significance":[]},{"end":140515450,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140515450,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs141372304"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795689802","source":"dbSNP","start":140515451,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140515451,"alleles":["G","A"],"feature_type":"variation","strand":1},{"end":140515452,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140515452,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1244683696","clinical_significance":[]},{"source":"dbSNP","start":140515455,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140515456,"alleles":["AG","AGAG"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1354345496"},{"start":140515456,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140515456,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs889864095","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515457,"feature_type":"variation","strand":1,"alleles":["T","TT"],"end":140515457,"clinical_significance":[],"id":"rs1795689873","seq_region_name":"7"},{"source":"dbSNP","start":140515460,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140515460,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585529953"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140515461,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515461,"clinical_significance":[],"seq_region_name":"7","id":"rs1795689908"},{"start":140515462,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140515462,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1308077537","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515463,"feature_type":"variation","strand":1,"end":140515463,"alleles":["A","G"],"clinical_significance":[],"id":"rs1165425677","seq_region_name":"7"},{"alleles":["A","G"],"end":140515464,"strand":1,"feature_type":"variation","start":140515464,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795689970","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795689990","clinical_significance":[],"alleles":["C","G"],"end":140515466,"strand":1,"feature_type":"variation","start":140515466,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1411326477","source":"dbSNP","start":140515468,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","G","T"],"end":140515468,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1585529959","clinical_significance":[],"start":140515469,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C"],"end":140515469,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140515470,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515470,"source":"dbSNP","id":"rs1585529963","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140515471,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515471,"source":"dbSNP","seq_region_name":"7","id":"rs1795690061","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140515473,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515473,"clinical_significance":[],"seq_region_name":"7","id":"rs1795690080"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515475,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140515475,"clinical_significance":[],"seq_region_name":"7","id":"rs1368334478"},{"seq_region_name":"7","id":"rs1795690120","clinical_significance":[],"start":140515476,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140515476,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs957207535","clinical_significance":[],"start":140515478,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140515478,"strand":1,"feature_type":"variation"},{"end":140515482,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140515482,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1363581700","clinical_significance":[]},{"source":"dbSNP","start":140515485,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140515485,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1405746744"},{"source":"dbSNP","start":140515486,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140515486,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1415625072","seq_region_name":"7"},{"alleles":["C","T"],"end":140515487,"strand":1,"feature_type":"variation","start":140515487,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585529980","clinical_significance":[]},{"start":140515488,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140515488,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1161452860","clinical_significance":[]},{"end":140515492,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140515492,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1007084486","clinical_significance":[]},{"source":"dbSNP","start":140515493,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140515493,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs576194971"},{"source":"dbSNP","start":140515494,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140515494,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585529986"},{"clinical_significance":[],"seq_region_name":"7","id":"rs968213048","end":140515495,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140515495,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795690329","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515499,"feature_type":"variation","strand":1,"alleles":["AA","A"],"end":140515500},{"clinical_significance":[],"seq_region_name":"7","id":"rs1000192753","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515502,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140515502},{"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140515505,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515505,"source":"dbSNP","seq_region_name":"7","id":"rs1298500234","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515509,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140515509,"clinical_significance":[],"seq_region_name":"7","id":"rs1795690375"},{"clinical_significance":[],"id":"rs1184411952","seq_region_name":"7","end":140515510,"alleles":["CC","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140515509,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140515512,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140515512,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs913174157","clinical_significance":[]},{"seq_region_name":"7","id":"rs1031212118","clinical_significance":[],"alleles":["C","G"],"end":140515514,"strand":1,"feature_type":"variation","start":140515514,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795690458","alleles":["C","T"],"end":140515520,"feature_type":"variation","strand":1,"source":"dbSNP","start":140515520,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs187464407","clinical_significance":[],"strand":1,"feature_type":"variation","end":140515522,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515522,"source":"dbSNP"},{"seq_region_name":"7","id":"rs868700336","clinical_significance":[],"start":140515529,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140515529,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140515530,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515530,"source":"dbSNP","seq_region_name":"7","id":"rs960399302","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515533,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140515533,"seq_region_name":"7","id":"rs1232522645","clinical_significance":[]},{"seq_region_name":"7","id":"rs1222507388","clinical_significance":[],"start":140515534,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["-","A"],"end":140515533,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs949997268","seq_region_name":"7","end":140515534,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140515534,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515535,"feature_type":"variation","strand":1,"end":140515535,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1288157952"},{"clinical_significance":[],"id":"rs1213664578","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140515536,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515536},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515537,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140515537,"id":"rs577212827","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","C"],"end":140515538,"strand":1,"feature_type":"variation","start":140515538,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795690640","clinical_significance":[]},{"seq_region_name":"7","id":"rs916360665","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515539,"source":"dbSNP","strand":1,"feature_type":"variation","end":140515539,"alleles":["A","C","G"]},{"alleles":["A","C","G"],"end":140515541,"strand":1,"feature_type":"variation","start":140515541,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs544266893","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1278607051","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515543,"feature_type":"variation","strand":1,"end":140515543,"alleles":["G","A"]},{"alleles":["A","C","G"],"end":140515544,"feature_type":"variation","strand":1,"source":"dbSNP","start":140515544,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1317804637","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1321307686","clinical_significance":[],"strand":1,"feature_type":"variation","end":140515546,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515546,"source":"dbSNP"},{"source":"dbSNP","start":140515547,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140515547,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1357899791","seq_region_name":"7"},{"alleles":["C","T"],"end":140515548,"feature_type":"variation","strand":1,"source":"dbSNP","start":140515548,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs200470473"},{"source":"dbSNP","start":140515549,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140515549,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs11769097"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795690928","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140515554,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515554},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515556,"feature_type":"variation","strand":1,"end":140515556,"alleles":["C","A","T"],"clinical_significance":[],"id":"rs75009904","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140515557,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515557,"source":"dbSNP","id":"rs1192059148","seq_region_name":"7","clinical_significance":[]},{"id":"rs909046860","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C","T"],"end":140515560,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515560,"source":"dbSNP"},{"source":"dbSNP","start":140515561,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140515561,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs940497223"},{"alleles":["T","A"],"end":140515564,"feature_type":"variation","strand":1,"source":"dbSNP","start":140515564,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs902120610"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515565,"source":"dbSNP","strand":1,"feature_type":"variation","end":140515565,"alleles":["A","G"],"id":"rs1270578127","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs998188837","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140515583,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515583},{"clinical_significance":[],"seq_region_name":"7","id":"rs1314678388","feature_type":"variation","strand":1,"end":140515587,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515587},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515589,"source":"dbSNP","strand":1,"feature_type":"variation","end":140515589,"alleles":["G","A"],"seq_region_name":"7","id":"rs542460687","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795691158","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515590,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140515590},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140515591,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515591,"source":"dbSNP","seq_region_name":"7","id":"rs1036728306","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515592,"feature_type":"variation","strand":1,"end":140515592,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs560627917"},{"id":"rs76692319","seq_region_name":"7","clinical_significance":[],"start":140515593,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140515593,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795691301","feature_type":"variation","strand":1,"end":140515597,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515597},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515599,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140515599,"seq_region_name":"7","id":"rs1369263022","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795691345","clinical_significance":[],"start":140515600,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140515600,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515602,"feature_type":"variation","strand":1,"end":140515602,"alleles":["A","C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1051078039"},{"alleles":["G","A"],"end":140515607,"feature_type":"variation","strand":1,"source":"dbSNP","start":140515607,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795691399"},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140515608,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515608,"clinical_significance":[],"seq_region_name":"7","id":"rs1795691414"},{"source":"dbSNP","start":140515612,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140515612,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795691430"},{"clinical_significance":[],"id":"rs1585530047","seq_region_name":"7","source":"dbSNP","start":140515618,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140515618,"alleles":["T","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795691479","alleles":["T","C"],"end":140515621,"feature_type":"variation","strand":1,"source":"dbSNP","start":140515621,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140515624,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140515624,"alleles":["A","G"],"strand":1,"feature_type":"variation","id":"rs1365580690","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140515628,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515628,"clinical_significance":[],"id":"rs1795691513","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1032755769","end":140515629,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140515629,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515630,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140515630,"seq_region_name":"7","id":"rs889769831","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795691567","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140515631,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515631,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795691594","clinical_significance":[],"alleles":["T","C","G"],"end":140515632,"strand":1,"feature_type":"variation","start":140515632,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140515636,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C","G"],"end":140515636,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs957101897","clinical_significance":[]},{"seq_region_name":"7","id":"rs1176852129","clinical_significance":[],"end":140515640,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140515640,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs988635584","seq_region_name":"7","clinical_significance":[],"start":140515641,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140515641,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795691675","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515644,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140515644},{"end":140515645,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140515645,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs546764576"},{"alleles":["C","T"],"end":140515647,"feature_type":"variation","strand":1,"source":"dbSNP","start":140515647,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795691721"},{"strand":1,"feature_type":"variation","end":140515648,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515648,"source":"dbSNP","seq_region_name":"7","id":"rs190580421","clinical_significance":[]},{"end":140515649,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140515649,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs763713242","seq_region_name":"7"},{"alleles":["C","A","T"],"end":140515657,"strand":1,"feature_type":"variation","start":140515657,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs942789816","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs757621060","end":140515660,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140515660,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140515661,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515661,"source":"dbSNP","seq_region_name":"7","id":"rs1563110281","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515662,"feature_type":"variation","strand":1,"end":140515662,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1423166644"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140515667,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515667,"source":"dbSNP","seq_region_name":"7","id":"rs1563110286","clinical_significance":[]},{"start":140515671,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140515671,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795691908","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1170960067","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515672,"feature_type":"variation","strand":1,"end":140515672,"alleles":["G","A"]},{"end":140515673,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140515673,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1450498171"},{"seq_region_name":"7","id":"rs1250276818","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140515675,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515675,"source":"dbSNP"},{"id":"rs532165288","seq_region_name":"7","clinical_significance":[],"alleles":["A","G"],"end":140515676,"strand":1,"feature_type":"variation","start":140515676,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs112815803","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140515678,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515678,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795692058","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140515680,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515680},{"seq_region_name":"7","id":"rs1329601899","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515683,"source":"dbSNP","strand":1,"feature_type":"variation","end":140515683,"alleles":["T","C","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1210238782","alleles":["C","G"],"end":140515688,"feature_type":"variation","strand":1,"source":"dbSNP","start":140515688,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140515693,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140515693,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1313403033"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515695,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140515695,"id":"rs1795692156","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","T"],"end":140515696,"strand":1,"feature_type":"variation","start":140515696,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1399773598","clinical_significance":[]},{"alleles":["C","T"],"end":140515697,"feature_type":"variation","strand":1,"source":"dbSNP","start":140515697,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795692193","seq_region_name":"7"},{"start":140515698,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140515698,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795692215","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1233091416","end":140515705,"alleles":["CTTCTT","CTT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140515700,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140515704,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515704,"clinical_significance":[],"seq_region_name":"7","id":"rs1380504755"},{"clinical_significance":[],"seq_region_name":"7","id":"rs143956884","feature_type":"variation","strand":1,"alleles":["TTTTTTTTT","TTTTTTTT","TTTTTTTTTT"],"end":140515712,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515704},{"strand":1,"feature_type":"variation","end":140515712,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515712,"source":"dbSNP","id":"rs999695682","seq_region_name":"7","clinical_significance":[]},{"end":140515713,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140515713,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585530117","clinical_significance":[]},{"start":140515717,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140515717,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1031246559","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795692400","seq_region_name":"7","source":"dbSNP","start":140515733,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140515733,"alleles":["A","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795692418","clinical_significance":[],"start":140515740,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140515740,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140515741,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140515741,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795692435"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795692462","source":"dbSNP","start":140515743,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140515743,"alleles":["A","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795692509","clinical_significance":[],"alleles":["C","G"],"end":140515745,"strand":1,"feature_type":"variation","start":140515745,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795692532","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515747,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140515747},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140515753,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515753,"clinical_significance":[],"id":"rs1795692560","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1795692577","seq_region_name":"7","alleles":["T","C"],"end":140515754,"feature_type":"variation","strand":1,"source":"dbSNP","start":140515754,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795692599","clinical_significance":[],"strand":1,"feature_type":"variation","end":140515755,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515755,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515764,"source":"dbSNP","strand":1,"feature_type":"variation","end":140515764,"alleles":["C","T"],"id":"rs1795692624","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515765,"source":"dbSNP","strand":1,"feature_type":"variation","end":140515765,"alleles":["A","G"],"seq_region_name":"7","id":"rs2130435045","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1453537184","end":140515767,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140515767,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs896729502","clinical_significance":[],"strand":1,"feature_type":"variation","end":140515768,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515768,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1795692698","seq_region_name":"7","source":"dbSNP","start":140515771,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140515771,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795692714","source":"dbSNP","start":140515773,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140515773,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515782,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140515782,"id":"rs1563110306","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1450300438","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515783,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140515783},{"source":"dbSNP","start":140515786,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140515786,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs746156738","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140515787,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515787,"source":"dbSNP","seq_region_name":"7","id":"rs1795692790","clinical_significance":[]},{"seq_region_name":"7","id":"rs937360245","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140515793,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515793,"source":"dbSNP"},{"source":"dbSNP","start":140515802,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140515802,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795692830"},{"seq_region_name":"7","id":"rs984787935","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515803,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140515803},{"seq_region_name":"7","id":"rs1312565299","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515805,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140515805},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515808,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140515808,"clinical_significance":[],"id":"rs1795692882","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140515814,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515814,"source":"dbSNP","id":"rs569152299","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795692927","clinical_significance":[],"end":140515815,"alleles":["A","-"],"strand":1,"feature_type":"variation","start":140515815,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1228264568","source":"dbSNP","start":140515818,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140515818,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1286462245","seq_region_name":"7","source":"dbSNP","start":140515819,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140515823,"alleles":["TTTTT","TTTT"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795692985","clinical_significance":[],"alleles":["T","G"],"end":140515823,"strand":1,"feature_type":"variation","start":140515823,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140515827,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515827,"clinical_significance":[],"seq_region_name":"7","id":"rs940741990"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515837,"feature_type":"variation","strand":1,"end":140515837,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795692998"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795693015","source":"dbSNP","start":140515840,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140515840,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140515845,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515845,"clinical_significance":[],"seq_region_name":"7","id":"rs1795693037"},{"seq_region_name":"7","id":"rs1795693047","clinical_significance":[],"end":140515846,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140515846,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515857,"feature_type":"variation","strand":1,"end":140515857,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130435107"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1428244536","source":"dbSNP","start":140515858,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["ATCAT","AT"],"end":140515862,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795693089","alleles":["T","C"],"end":140515859,"feature_type":"variation","strand":1,"source":"dbSNP","start":140515859,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1415200544","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515861,"feature_type":"variation","strand":1,"end":140515861,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs1023271083","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515862,"source":"dbSNP","strand":1,"feature_type":"variation","end":140515862,"alleles":["T","C"]},{"alleles":["T","C"],"end":140515863,"feature_type":"variation","strand":1,"source":"dbSNP","start":140515863,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs968993131"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1254765564","feature_type":"variation","strand":1,"end":140515864,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515864},{"clinical_significance":[],"seq_region_name":"7","id":"rs1036419913","source":"dbSNP","start":140515865,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140515865,"alleles":["T","A","C"],"feature_type":"variation","strand":1},{"alleles":["T","C"],"end":140515868,"feature_type":"variation","strand":1,"source":"dbSNP","start":140515868,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795693400"},{"source":"dbSNP","start":140515869,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140515869,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1483164009"},{"start":140515870,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140515870,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1349209923","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140515871,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515871,"clinical_significance":[],"seq_region_name":"7","id":"rs984950284"},{"alleles":["T","C"],"end":140515873,"feature_type":"variation","strand":1,"source":"dbSNP","start":140515873,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1257082420"},{"start":140515875,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140515875,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795693508","clinical_significance":[]},{"start":140515881,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140515881,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs1795693525","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs933462803","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515887,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140515887},{"start":140515888,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","-"],"end":140515888,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1051125045","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795693590","clinical_significance":[],"alleles":["CAAG","-"],"end":140515891,"strand":1,"feature_type":"variation","start":140515888,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795693599","clinical_significance":[],"alleles":["-","T","TAGGCTGGCGCCAGTCT"],"end":140515888,"strand":1,"feature_type":"variation","start":140515889,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140515889,"alleles":["A","C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515889,"source":"dbSNP","seq_region_name":"7","id":"rs4726880","clinical_significance":[]},{"end":140515889,"alleles":["-","GGCTGGCGCCAGTCTG"],"strand":1,"feature_type":"variation","start":140515890,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795693703","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515892,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140515892,"seq_region_name":"7","id":"rs1795693719","clinical_significance":[]},{"clinical_significance":[],"id":"rs2130435157","seq_region_name":"7","feature_type":"variation","strand":1,"end":140515893,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515893},{"seq_region_name":"7","id":"rs554351878","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515894,"source":"dbSNP","strand":1,"feature_type":"variation","end":140515894,"alleles":["T","G"]},{"seq_region_name":"7","id":"rs1006548971","clinical_significance":[],"start":140515897,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140515897,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs971910996","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515898,"feature_type":"variation","strand":1,"end":140515898,"alleles":["G","A"]},{"feature_type":"variation","strand":1,"end":140515901,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515901,"clinical_significance":[],"seq_region_name":"7","id":"rs2130435170"},{"seq_region_name":"7","id":"rs1795693806","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515902,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140515902},{"seq_region_name":"7","id":"rs1482613055","clinical_significance":[],"end":140515903,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140515903,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs73492319","clinical_significance":[],"end":140515904,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140515904,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1372670878","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515908,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140515908},{"clinical_significance":[],"seq_region_name":"7","id":"rs933245934","alleles":["C","G"],"end":140515910,"feature_type":"variation","strand":1,"source":"dbSNP","start":140515910,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515911,"feature_type":"variation","strand":1,"end":140515911,"alleles":["T","C"],"clinical_significance":[],"id":"rs1795693934","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140515912,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515912,"clinical_significance":[],"id":"rs1795693952","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1009962133","seq_region_name":"7","end":140515915,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140515915,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1795693992","seq_region_name":"7","end":140515916,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140515916,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1585530205","seq_region_name":"7","source":"dbSNP","start":140515922,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140515922,"alleles":["T","C","G"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515924,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140515924,"clinical_significance":[],"seq_region_name":"7","id":"rs1585530210"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795694042","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515926,"feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140515926},{"start":140515927,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140515929,"alleles":["GGG","GG"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1350775950","clinical_significance":[]},{"end":140515928,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140515928,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795694074","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140515929,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515929,"clinical_significance":[],"seq_region_name":"7","id":"rs1795694085"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130435209","feature_type":"variation","strand":1,"end":140515931,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515931},{"end":140515937,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140515937,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs986015140","seq_region_name":"7"},{"source":"dbSNP","start":140515942,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140515942,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1585530219","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515943,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140515943,"clinical_significance":[],"seq_region_name":"7","id":"rs533733471"},{"seq_region_name":"7","id":"rs1415082930","clinical_significance":[],"strand":1,"feature_type":"variation","end":140515946,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515946,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1186627276","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","C","T"],"end":140515947,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515947},{"id":"rs1423235947","seq_region_name":"7","clinical_significance":[],"start":140515948,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140515948,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1795694232","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515952,"source":"dbSNP","strand":1,"feature_type":"variation","end":140515952,"alleles":["T","C"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515953,"feature_type":"variation","strand":1,"alleles":["TGTGTGT","TGTGT"],"end":140515959,"clinical_significance":[],"id":"rs1470423979","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs775676388","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515954,"feature_type":"variation","strand":1,"end":140515954,"alleles":["G","A","C"]},{"clinical_significance":[],"id":"rs1795694313","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515955,"feature_type":"variation","strand":1,"alleles":["-","A"],"end":140515954},{"clinical_significance":[],"seq_region_name":"7","id":"rs1034720852","source":"dbSNP","start":140515955,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140515955,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563110359","source":"dbSNP","start":140515957,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140515957,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515957,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TGTCTGT","TGT"],"end":140515963,"seq_region_name":"7","id":"rs1357504727","clinical_significance":[]},{"seq_region_name":"7","id":"rs1265809804","clinical_significance":[],"alleles":["G","A"],"end":140515958,"strand":1,"feature_type":"variation","start":140515958,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140515959,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515959,"source":"dbSNP","id":"rs1795694418","seq_region_name":"7","clinical_significance":[]},{"start":140515966,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140515966,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795694433","clinical_significance":[]},{"alleles":["CC","CCC"],"end":140515971,"feature_type":"variation","strand":1,"source":"dbSNP","start":140515970,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs35727124"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515972,"source":"dbSNP","strand":1,"feature_type":"variation","end":140515972,"alleles":["A","G"],"id":"rs1447335693","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1289990690","alleles":["G","C"],"end":140515984,"feature_type":"variation","strand":1,"source":"dbSNP","start":140515984,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140515985,"alleles":["C","-"],"strand":1,"feature_type":"variation","start":140515985,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1563110368","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs376910716","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515988,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140515988},{"clinical_significance":[],"id":"rs1292546642","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140515991,"feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140515991},{"seq_region_name":"7","id":"rs903928164","clinical_significance":[],"strand":1,"feature_type":"variation","end":140515995,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140515995,"source":"dbSNP"},{"clinical_significance":[],"id":"rs935526210","seq_region_name":"7","source":"dbSNP","start":140515997,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140515997,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140515999,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140515999,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795694604"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1352345474","source":"dbSNP","start":140516001,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140516001,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1398579684","end":140516002,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140516002,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795694656","clinical_significance":[],"start":140516009,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["-","GGCTGT","GGCTGTAC"],"end":140516008,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516010,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["-","ATGAC"],"end":140516009,"seq_region_name":"7","id":"rs1795694675","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516010,"feature_type":"variation","strand":1,"end":140516010,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1284287241"},{"seq_region_name":"7","id":"rs1795694714","clinical_significance":[],"end":140516010,"alleles":["-","A","ACA"],"strand":1,"feature_type":"variation","start":140516011,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["G","A"],"end":140516011,"feature_type":"variation","strand":1,"source":"dbSNP","start":140516011,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs577245664"},{"seq_region_name":"7","id":"rs1795694757","clinical_significance":[],"alleles":["GT","-"],"end":140516012,"strand":1,"feature_type":"variation","start":140516011,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["T","A","G"],"end":140516013,"strand":1,"feature_type":"variation","start":140516013,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1368792992","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140516015,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516015,"clinical_significance":[],"seq_region_name":"7","id":"rs984817388"},{"end":140516016,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140516016,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1460154458","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1323884341","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516018,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140516018},{"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140516022,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516022,"clinical_significance":[],"seq_region_name":"7","id":"rs1795694862"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563110378","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140516023,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516023},{"alleles":["C","T"],"end":140516026,"feature_type":"variation","strand":1,"source":"dbSNP","start":140516026,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1160469596","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs909224263","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516028,"feature_type":"variation","strand":1,"end":140516028,"alleles":["C","G","T"]},{"clinical_significance":[],"id":"rs557790933","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516036,"feature_type":"variation","strand":1,"end":140516036,"alleles":["T","C","G"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516038,"feature_type":"variation","strand":1,"end":140516038,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs940648191"},{"source":"dbSNP","start":140516040,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140516040,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130435306"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140516043,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516043,"source":"dbSNP","seq_region_name":"7","id":"rs1418121172","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130435309","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516046,"feature_type":"variation","strand":1,"end":140516046,"alleles":["T","C"]},{"end":140516047,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140516047,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795694982"},{"alleles":["A","G"],"end":140516051,"strand":1,"feature_type":"variation","start":140516051,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs544617502","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795695028","clinical_significance":[],"alleles":["G","T"],"end":140516054,"strand":1,"feature_type":"variation","start":140516054,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795695043","clinical_significance":[],"alleles":["T","C"],"end":140516057,"strand":1,"feature_type":"variation","start":140516057,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140516058,"alleles":["G","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516058,"source":"dbSNP","id":"rs2130435327","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","C"],"end":140516059,"feature_type":"variation","strand":1,"source":"dbSNP","start":140516059,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795695064","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1267855852","clinical_significance":[],"alleles":["G","A"],"end":140516068,"strand":1,"feature_type":"variation","start":140516068,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["A","G"],"end":140516070,"feature_type":"variation","strand":1,"source":"dbSNP","start":140516070,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1192729278"},{"start":140516072,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140516072,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1466942472","clinical_significance":[]},{"clinical_significance":[],"id":"rs183105994","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516074,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140516074},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516075,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140516075,"clinical_significance":[],"seq_region_name":"7","id":"rs575086693"},{"clinical_significance":[],"seq_region_name":"7","id":"rs34683196","feature_type":"variation","strand":1,"alleles":["T","TT"],"end":140516076,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516076},{"start":140516076,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140516076,"alleles":["T","C","G"],"strand":1,"feature_type":"variation","id":"rs896634839","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1238662735","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516078,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140516078},{"start":140516083,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A","C","G"],"end":140516083,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1013800013","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1439163639","alleles":["C","G","T"],"end":140516084,"feature_type":"variation","strand":1,"source":"dbSNP","start":140516084,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1023804241","clinical_significance":[],"alleles":["C","A"],"end":140516086,"strand":1,"feature_type":"variation","start":140516086,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140516087,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516087,"source":"dbSNP","seq_region_name":"7","id":"rs1050612117","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1437893833","end":140516088,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140516088,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1795695613","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140516091,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516091,"source":"dbSNP"},{"end":140516094,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140516094,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795695638","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516096,"feature_type":"variation","strand":1,"end":140516096,"alleles":["C","T"],"clinical_significance":[],"id":"rs889396692","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs904897656","source":"dbSNP","start":140516097,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140516097,"alleles":["C","T"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516098,"source":"dbSNP","strand":1,"feature_type":"variation","end":140516098,"alleles":["C","T"],"id":"rs1005878079","seq_region_name":"7","clinical_significance":[]},{"id":"rs1053941964","seq_region_name":"7","clinical_significance":[],"start":140516105,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140516105,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1484835584","end":140516108,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140516108,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140516125,"alleles":["GGAGCCAAGGCGGGCGGA","GGA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140516108,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs764446312"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1175059532","feature_type":"variation","strand":1,"end":140516111,"alleles":["G","GG"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516111},{"seq_region_name":"7","id":"rs1795695857","clinical_significance":[],"end":140516111,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140516111,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140516112,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140516112,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795695902"},{"start":140516113,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140516113,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1452360470","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1252136183","source":"dbSNP","start":140516114,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140516114,"alleles":["A","G"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140516116,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516116,"clinical_significance":[],"seq_region_name":"7","id":"rs892809624"},{"seq_region_name":"7","id":"rs1009871474","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140516118,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516118,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1016456809","source":"dbSNP","start":140516119,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140516119,"alleles":["G","A","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs747112452","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516122,"feature_type":"variation","strand":1,"end":140516122,"alleles":["C","A","T"]},{"alleles":["G","A"],"end":140516123,"strand":1,"feature_type":"variation","start":140516123,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs971785685","clinical_significance":[]},{"seq_region_name":"7","id":"rs1481255956","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516124,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140516124},{"start":140516125,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140516125,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585530326","clinical_significance":[]},{"end":140516129,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140516129,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795696200"},{"feature_type":"variation","strand":1,"end":140516135,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516135,"clinical_significance":[],"seq_region_name":"7","id":"rs1347697016"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1030185573","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516145,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140516145},{"clinical_significance":[],"seq_region_name":"7","id":"rs780737575","alleles":["G","A"],"end":140516148,"feature_type":"variation","strand":1,"source":"dbSNP","start":140516148,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1795696336","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140516150,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516150,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795696354","alleles":["CC","C"],"end":140516151,"feature_type":"variation","strand":1,"source":"dbSNP","start":140516150,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140516152,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140516152,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs954491562","clinical_significance":[]},{"alleles":["C","A"],"end":140516154,"feature_type":"variation","strand":1,"source":"dbSNP","start":140516154,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs542497467"},{"clinical_significance":[],"id":"rs910467482","seq_region_name":"7","source":"dbSNP","start":140516155,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140516155,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140516159,"alleles":["T","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516159,"clinical_significance":[],"seq_region_name":"7","id":"rs11761212"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1016149077","alleles":["C","T"],"end":140516160,"feature_type":"variation","strand":1,"source":"dbSNP","start":140516160,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140516162,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140516162,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795696585","seq_region_name":"7"},{"source":"dbSNP","start":140516163,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140516163,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795696615"},{"seq_region_name":"7","id":"rs1795696638","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516164,"source":"dbSNP","strand":1,"feature_type":"variation","end":140516164,"alleles":["A","G"]},{"clinical_significance":[],"id":"rs1432478948","seq_region_name":"7","feature_type":"variation","strand":1,"end":140516165,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516165},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516167,"feature_type":"variation","strand":1,"end":140516167,"alleles":["G","A"],"clinical_significance":[],"id":"rs11769944","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1394300124","clinical_significance":[],"end":140516168,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140516168,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs11760346","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516174,"feature_type":"variation","strand":1,"end":140516174,"alleles":["A","C"]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140516176,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516176,"clinical_significance":[],"id":"rs1418391488","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs769800275","end":140516177,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140516177,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795696858","clinical_significance":[],"start":140516178,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140516178,"alleles":["T","C","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs560766343","clinical_significance":[],"start":140516179,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140516179,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795696925","end":140516180,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140516180,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140516182,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140516182,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1346548054","clinical_significance":[]},{"id":"rs11769946","seq_region_name":"7","clinical_significance":[],"end":140516183,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140516183,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795696999","clinical_significance":[],"strand":1,"feature_type":"variation","end":140516184,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516184,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["AAAAA","AAAA"],"end":140516190,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516186,"clinical_significance":[],"seq_region_name":"7","id":"rs1795697022"},{"seq_region_name":"7","id":"rs925382281","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516189,"source":"dbSNP","strand":1,"feature_type":"variation","end":140516189,"alleles":["A","T"]},{"seq_region_name":"7","id":"rs1795697067","clinical_significance":[],"start":140516190,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140516190,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs972080838","clinical_significance":[],"end":140516192,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140516192,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140516193,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516193,"clinical_significance":[],"seq_region_name":"7","id":"rs923388601"},{"seq_region_name":"7","id":"rs1795697160","clinical_significance":[],"start":140516194,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AAAAA","AAAAAA"],"end":140516198,"strand":1,"feature_type":"variation"},{"start":140516198,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140516198,"alleles":["A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795697184","clinical_significance":[]},{"seq_region_name":"7","id":"rs954797442","clinical_significance":[],"end":140516202,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140516202,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1485455717","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516204,"source":"dbSNP","strand":1,"feature_type":"variation","end":140516204,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1795697258","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140516205,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516205,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1275562897","clinical_significance":[],"start":140516206,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140516206,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1207780857","clinical_significance":[],"end":140516207,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140516207,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs986594965","seq_region_name":"7","clinical_significance":[],"start":140516209,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140516209,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"start":140516210,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140516210,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795697396","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795697416","source":"dbSNP","start":140516212,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140516212,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs572952781","clinical_significance":[],"start":140516216,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140516216,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140516217,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516217,"clinical_significance":[],"seq_region_name":"7","id":"rs540393682"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516218,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140516218,"clinical_significance":[],"id":"rs936805461","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1053974758","clinical_significance":[],"start":140516219,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140516219,"alleles":["C","G","T"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516220,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140516220,"clinical_significance":[],"seq_region_name":"7","id":"rs112126583"},{"clinical_significance":[],"id":"rs949553984","seq_region_name":"7","alleles":["G","A","T"],"end":140516221,"feature_type":"variation","strand":1,"source":"dbSNP","start":140516221,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["T","C"],"end":140516224,"feature_type":"variation","strand":1,"source":"dbSNP","start":140516224,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795697683"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585530387","alleles":["G","A"],"end":140516225,"feature_type":"variation","strand":1,"source":"dbSNP","start":140516225,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516227,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140516227,"clinical_significance":[],"seq_region_name":"7","id":"rs945742588"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140516228,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516228,"clinical_significance":[],"seq_region_name":"7","id":"rs1394051047"},{"id":"rs1215812795","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140516230,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516230,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140516231,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516231,"source":"dbSNP","seq_region_name":"7","id":"rs1585530400","clinical_significance":[]},{"seq_region_name":"7","id":"rs1041366631","clinical_significance":[],"start":140516233,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140516233,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140516234,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516234,"source":"dbSNP","id":"rs1420176976","seq_region_name":"7","clinical_significance":[]},{"id":"rs1292355936","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140516235,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516235,"source":"dbSNP"},{"alleles":["T","C"],"end":140516239,"strand":1,"feature_type":"variation","start":140516239,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795697944","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585530410","alleles":["A","T"],"end":140516241,"feature_type":"variation","strand":1,"source":"dbSNP","start":140516241,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140516243,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140516243,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1045325118","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs906976042","source":"dbSNP","start":140516245,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140516245,"alleles":["G","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1474898338","end":140516249,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140516249,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs546405215","source":"dbSNP","start":140516250,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140516250,"feature_type":"variation","strand":1},{"end":140516252,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140516252,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs905433033","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795698129","alleles":["GGGGG","GGGGGG"],"end":140516256,"feature_type":"variation","strand":1,"source":"dbSNP","start":140516252,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795698154","source":"dbSNP","start":140516253,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C","T"],"end":140516253,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795698176","end":140516256,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140516256,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1206823832","seq_region_name":"7","end":140516261,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140516261,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1436494341","alleles":["C","G","T"],"end":140516262,"feature_type":"variation","strand":1,"source":"dbSNP","start":140516262,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs373942339","clinical_significance":[],"start":140516263,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C","T"],"end":140516263,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516270,"source":"dbSNP","strand":1,"feature_type":"variation","end":140516270,"alleles":["C","T"],"seq_region_name":"7","id":"rs1795698280","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516271,"feature_type":"variation","strand":1,"end":140516271,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1245238148"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140516272,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516272,"source":"dbSNP","seq_region_name":"7","id":"rs532079595","clinical_significance":[]},{"seq_region_name":"7","id":"rs370193349","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516273,"source":"dbSNP","strand":1,"feature_type":"variation","end":140516273,"alleles":["G","A","C"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516277,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140516277,"clinical_significance":[],"seq_region_name":"7","id":"rs1795698398"},{"start":140516279,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140516279,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1410267530","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516281,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140516281,"clinical_significance":[],"seq_region_name":"7","id":"rs1795698453"},{"seq_region_name":"7","id":"rs1795698482","clinical_significance":[],"end":140516282,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140516282,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140516283,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516283,"source":"dbSNP","seq_region_name":"7","id":"rs1795698496","clinical_significance":[]},{"seq_region_name":"7","id":"rs766256802","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","C","T"],"end":140516284,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516284,"source":"dbSNP"},{"end":140516285,"alleles":["T","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140516285,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795698578"},{"clinical_significance":[],"id":"rs1795698625","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516287,"feature_type":"variation","strand":1,"end":140516287,"alleles":["G","A"]},{"feature_type":"variation","strand":1,"end":140516290,"alleles":["GCAG","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516287,"clinical_significance":[],"id":"rs1795698646","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795698680","feature_type":"variation","strand":1,"alleles":["GCAGTGAGCCAAGATCGTGCCGCTGCACTCCAGCCTGGGGGACAGAGC","GC"],"end":140516334,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516287},{"id":"rs993252375","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516289,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140516289},{"seq_region_name":"7","id":"rs1795698763","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516292,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GAGCCAAGA","-"],"end":140516300},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795698803","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516294,"feature_type":"variation","strand":1,"end":140516294,"alleles":["G","A"]},{"clinical_significance":[],"id":"rs961983823","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140516296,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516296},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140516297,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516297,"source":"dbSNP","id":"rs993927980","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1030346792","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140516299,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516299},{"alleles":["T","C"],"end":140516301,"feature_type":"variation","strand":1,"source":"dbSNP","start":140516301,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1396641734"},{"end":140516302,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140516302,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs954851123","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795699064","clinical_significance":[],"end":140516334,"alleles":["CGTGCCGCTGCACTCCAGCCTGGGGGACAGAGC","-"],"strand":1,"feature_type":"variation","start":140516302,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1030044870","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516303,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140516303},{"seq_region_name":"7","id":"rs1321953268","clinical_significance":[],"strand":1,"feature_type":"variation","end":140516304,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516304,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1349013914","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516305,"feature_type":"variation","strand":1,"end":140516305,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1412784741","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140516307,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516307,"source":"dbSNP"},{"seq_region_name":"7","id":"rs56332580","clinical_significance":[],"end":140516308,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140516308,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140516308,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["GCTGCACTCCAGC","GC"],"end":140516320,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs200239271"},{"seq_region_name":"7","id":"rs1468772663","clinical_significance":[],"strand":1,"feature_type":"variation","end":140516309,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516309,"source":"dbSNP"},{"end":140516310,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140516310,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs958234995","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1007389723","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140516311,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516311},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516320,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140516320,"seq_region_name":"7","id":"rs1017967416","clinical_significance":[]},{"clinical_significance":[],"id":"rs914179053","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516322,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140516322},{"seq_region_name":"7","id":"rs968645370","clinical_significance":[],"start":140516324,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140516324,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs4726881","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","C","T"],"end":140516326,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516326,"source":"dbSNP"},{"end":140516327,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140516327,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs867676015","seq_region_name":"7","clinical_significance":[]},{"end":140516328,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140516328,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1348128566","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140516330,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516330,"clinical_significance":[],"seq_region_name":"7","id":"rs1795700002"},{"seq_region_name":"7","id":"rs1795700037","clinical_significance":[],"start":140516331,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140516331,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs868316632","feature_type":"variation","strand":1,"end":140516332,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516332},{"end":140516334,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140516334,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs928338303","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795700171","source":"dbSNP","start":140516334,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","CTC"],"end":140516334,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140516335,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140516335,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs113028672","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795700335","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516337,"source":"dbSNP","strand":1,"feature_type":"variation","end":140516337,"alleles":["G","C"]},{"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140516339,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516339,"clinical_significance":[],"seq_region_name":"7","id":"rs2130435832"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516343,"feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140516343,"clinical_significance":[],"seq_region_name":"7","id":"rs925321174"},{"clinical_significance":[],"id":"rs1795700431","seq_region_name":"7","source":"dbSNP","start":140516345,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140516345,"feature_type":"variation","strand":1},{"id":"rs1323879098","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516347,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140516347},{"id":"rs879923899","seq_region_name":"7","clinical_significance":[],"start":140516348,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140516360,"alleles":["AAAAAAAAAAAAA","AAAAAAAAAA","AAAAAAAAAAA","AAAAAAAAAAAA","AAAAAAAAAAAAAA","AAAAAAAAAAAAAAA"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1161355735","clinical_significance":[],"start":140516350,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140516350,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1398980245","clinical_significance":[],"start":140516351,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140516351,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1407529366","seq_region_name":"7","source":"dbSNP","start":140516353,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AAAAAAAAGTAAATAAATTTAAAAAAAAGTA","AAAAAAAAGTA"],"end":140516383,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140516354,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516354,"clinical_significance":[],"seq_region_name":"7","id":"rs2130435866"},{"strand":1,"feature_type":"variation","end":140516356,"alleles":["A","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516356,"source":"dbSNP","seq_region_name":"7","id":"rs1585530506","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516358,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AAAG","-"],"end":140516361,"id":"rs1173318285","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795700777","seq_region_name":"7","source":"dbSNP","start":140516359,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["-","C"],"end":140516358,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795700802","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516359,"source":"dbSNP","strand":1,"feature_type":"variation","end":140516359,"alleles":["A","G"]},{"clinical_significance":[],"id":"rs1795700829","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["-","C"],"end":140516359,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516360},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585530511","alleles":["T","A"],"end":140516362,"feature_type":"variation","strand":1,"source":"dbSNP","start":140516362,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1795700876","seq_region_name":"7","alleles":["A","G"],"end":140516363,"feature_type":"variation","strand":1,"source":"dbSNP","start":140516363,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795700904","end":140516368,"alleles":["AATAA","AA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140516364,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1455896615","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516365,"feature_type":"variation","strand":1,"end":140516365,"alleles":["A","G"]},{"clinical_significance":[],"id":"rs749306319","seq_region_name":"7","end":140516368,"alleles":["A","C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140516368,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1795700999","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140516369,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516369,"source":"dbSNP"},{"seq_region_name":"7","id":"rs566418948","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516372,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140516372},{"seq_region_name":"7","id":"rs533767571","clinical_significance":[],"start":140516373,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C","T"],"end":140516373,"strand":1,"feature_type":"variation"},{"end":140516380,"alleles":["AAAAAAAA","AAAAAAA","AAAAAAAAA"],"strand":1,"feature_type":"variation","start":140516373,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1244286043","seq_region_name":"7","clinical_significance":[]},{"end":140516380,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140516380,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585530530"},{"strand":1,"feature_type":"variation","alleles":["G","-"],"end":140516381,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516381,"source":"dbSNP","seq_region_name":"7","id":"rs1240222502","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795701173","alleles":["T","G"],"end":140516382,"feature_type":"variation","strand":1,"source":"dbSNP","start":140516382,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140516383,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140516383,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs142039178","clinical_significance":[]},{"alleles":["T","C"],"end":140516384,"feature_type":"variation","strand":1,"source":"dbSNP","start":140516384,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1585530541","seq_region_name":"7"},{"clinical_significance":[],"id":"rs184681614","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516387,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140516387},{"seq_region_name":"7","id":"rs1386453863","clinical_significance":[],"start":140516388,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140516388,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs528054004","seq_region_name":"7","alleles":["T","C"],"end":140516390,"feature_type":"variation","strand":1,"source":"dbSNP","start":140516390,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140516393,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140516393,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1007509855"},{"clinical_significance":[],"id":"rs1362604603","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516395,"feature_type":"variation","strand":1,"end":140516395,"alleles":["C","T"]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140516396,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516396,"clinical_significance":[],"seq_region_name":"7","id":"rs1017682574"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516398,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140516398,"seq_region_name":"7","id":"rs1428733509","clinical_significance":[]},{"seq_region_name":"7","id":"rs958097633","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140516401,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516401,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140516404,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516404,"source":"dbSNP","seq_region_name":"7","id":"rs1795701525","clinical_significance":[]},{"start":140516406,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140516406,"strand":1,"feature_type":"variation","id":"rs1795701552","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140516414,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516414,"source":"dbSNP","seq_region_name":"7","id":"rs1335179803","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795701588","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140516417,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516417},{"id":"rs1795701617","seq_region_name":"7","clinical_significance":[],"start":140516422,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140516422,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140516423,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140516423,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs989636903"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795701667","source":"dbSNP","start":140516424,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140516424,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1393710094","alleles":["C","G","T"],"end":140516425,"feature_type":"variation","strand":1,"source":"dbSNP","start":140516425,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140516426,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516426,"source":"dbSNP","id":"rs1021136980","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140516428,"alleles":["G","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516428,"clinical_significance":[],"seq_region_name":"7","id":"rs1450435958"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516430,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140516430,"seq_region_name":"7","id":"rs1413544792","clinical_significance":[]},{"end":140516438,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140516438,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1410839496","clinical_significance":[]},{"source":"dbSNP","start":140516441,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["CTTGTACA","CTTGTACATCTTGTACA"],"end":140516448,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1185231864"},{"source":"dbSNP","start":140516443,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140516443,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1474174918"},{"seq_region_name":"7","id":"rs1795701993","clinical_significance":[],"strand":1,"feature_type":"variation","end":140516445,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516445,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs967255613","end":140516447,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140516447,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140516450,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140516450,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795702091","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140516454,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516454,"clinical_significance":[],"id":"rs1795702131","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516455,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140516455,"seq_region_name":"7","id":"rs1211210269","clinical_significance":[]},{"seq_region_name":"7","id":"rs1563110496","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516456,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140516456},{"seq_region_name":"7","id":"rs1330499768","clinical_significance":[],"alleles":["TTTT","TTT"],"end":140516461,"strand":1,"feature_type":"variation","start":140516458,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140516462,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140516462,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795702317","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140516463,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516463,"source":"dbSNP","seq_region_name":"7","id":"rs6950168","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795702445","end":140516465,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140516465,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516466,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140516466,"clinical_significance":[],"seq_region_name":"7","id":"rs1038327297"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140516467,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516467,"source":"dbSNP","id":"rs1795702518","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1445453963","clinical_significance":[],"start":140516469,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140516469,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140516473,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516473,"clinical_significance":[],"seq_region_name":"7","id":"rs1336808735"},{"clinical_significance":[],"seq_region_name":"7","id":"rs928172029","source":"dbSNP","start":140516474,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140516474,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1209891700","seq_region_name":"7","feature_type":"variation","strand":1,"end":140516479,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516479},{"alleles":["TGG","-"],"end":140516485,"feature_type":"variation","strand":1,"source":"dbSNP","start":140516483,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1307797453"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516489,"source":"dbSNP","strand":1,"feature_type":"variation","end":140516489,"alleles":["C","A","T"],"seq_region_name":"7","id":"rs938394839","clinical_significance":[]},{"seq_region_name":"7","id":"rs764517230","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516490,"source":"dbSNP","strand":1,"feature_type":"variation","end":140516490,"alleles":["G","A"]},{"alleles":["T","C"],"end":140516491,"feature_type":"variation","strand":1,"source":"dbSNP","start":140516491,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs574789573"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1051544424","source":"dbSNP","start":140516493,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140516493,"alleles":["C","G","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1373904401","feature_type":"variation","strand":1,"end":140516495,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516495},{"feature_type":"variation","strand":1,"end":140516497,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516497,"clinical_significance":[],"seq_region_name":"7","id":"rs1795703082"},{"feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140516498,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516498,"clinical_significance":[],"seq_region_name":"7","id":"rs890194709"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140516499,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516499,"source":"dbSNP","id":"rs1216061060","seq_region_name":"7","clinical_significance":[]},{"id":"rs1462826950","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140516503,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516503,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140516505,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516505,"clinical_significance":[],"seq_region_name":"7","id":"rs1795703253"},{"strand":1,"feature_type":"variation","end":140516506,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516506,"source":"dbSNP","seq_region_name":"7","id":"rs1260294967","clinical_significance":[]},{"start":140516507,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140516507,"alleles":["A","-"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs772998851","clinical_significance":[]},{"start":140516508,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140516508,"alleles":["G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1316265043","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1428413575","end":140516509,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140516509,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795703511","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516510,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140516510},{"start":140516515,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140516515,"strand":1,"feature_type":"variation","id":"rs1795703555","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140516525,"alleles":["T","TTTT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516525,"source":"dbSNP","seq_region_name":"7","id":"rs1795703593","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516526,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140516526,"clinical_significance":[],"seq_region_name":"7","id":"rs1795703640"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795703679","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516527,"feature_type":"variation","strand":1,"end":140516527,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs2130436226","clinical_significance":[],"strand":1,"feature_type":"variation","end":140516528,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516528,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516529,"feature_type":"variation","strand":1,"alleles":["-","G"],"end":140516528,"clinical_significance":[],"seq_region_name":"7","id":"rs1795703720"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516531,"feature_type":"variation","strand":1,"end":140516531,"alleles":["C","G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1418233757"},{"clinical_significance":[],"id":"rs2130436242","seq_region_name":"7","feature_type":"variation","strand":1,"end":140516533,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516533},{"id":"rs1795703827","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516535,"source":"dbSNP","strand":1,"feature_type":"variation","end":140516535,"alleles":["T","C"]},{"end":140516537,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140516537,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795703928","clinical_significance":[]},{"source":"dbSNP","start":140516538,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140516538,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585530682"},{"alleles":["C","T"],"end":140516541,"feature_type":"variation","strand":1,"source":"dbSNP","start":140516541,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1198163433","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516543,"feature_type":"variation","strand":1,"end":140516543,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795704059"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516548,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140516548,"seq_region_name":"7","id":"rs2130436277","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140516549,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516549,"source":"dbSNP","seq_region_name":"7","id":"rs897662826","clinical_significance":[]},{"end":140516552,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140516552,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795704153"},{"clinical_significance":[],"id":"rs1243810369","seq_region_name":"7","end":140516560,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140516560,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516565,"feature_type":"variation","strand":1,"end":140516565,"alleles":["G","-"],"clinical_significance":[],"seq_region_name":"7","id":"rs760464827"},{"id":"rs1758241075","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140516568,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516568,"source":"dbSNP"},{"seq_region_name":"7","id":"rs867688674","clinical_significance":[],"alleles":["T","A","C"],"end":140516569,"strand":1,"feature_type":"variation","start":140516569,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs929099949","clinical_significance":[],"start":140516569,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TT","TTT"],"end":140516570,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1306867798","alleles":["G","A"],"end":140516573,"feature_type":"variation","strand":1,"source":"dbSNP","start":140516573,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516574,"feature_type":"variation","strand":1,"end":140516574,"alleles":["A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1273693443"},{"clinical_significance":[],"id":"rs1795704566","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516583,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140516583},{"alleles":["A","G"],"end":140516585,"strand":1,"feature_type":"variation","start":140516585,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1017455765","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","C"],"end":140516586,"strand":1,"feature_type":"variation","start":140516586,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795704633","clinical_significance":[]},{"end":140516587,"alleles":["A","G","T"],"strand":1,"feature_type":"variation","start":140516587,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs968927574","clinical_significance":[]},{"seq_region_name":"7","id":"rs1353579351","clinical_significance":[],"start":140516588,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140516588,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140516592,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516592,"clinical_significance":[],"id":"rs1292971783","seq_region_name":"7"},{"end":140516593,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140516593,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130436372"},{"feature_type":"variation","strand":1,"end":140516594,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516594,"clinical_significance":[],"seq_region_name":"7","id":"rs1017546717"},{"clinical_significance":[],"id":"rs1000120350","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140516596,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516596},{"source":"dbSNP","start":140516600,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140516600,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795704846"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516608,"feature_type":"variation","strand":1,"end":140516608,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585530737"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795704912","source":"dbSNP","start":140516611,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140516611,"alleles":["A","-"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795704947","clinical_significance":[],"alleles":["T","C"],"end":140516612,"strand":1,"feature_type":"variation","start":140516612,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140516614,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140516614,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1186058436"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1296791018","source":"dbSNP","start":140516619,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140516623,"alleles":["AACAA","AA"],"feature_type":"variation","strand":1},{"end":140516629,"alleles":["AATATAAT","AAT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140516622,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795705058","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1461758900","clinical_significance":[],"strand":1,"feature_type":"variation","end":140516625,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516625,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1237362102","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516626,"feature_type":"variation","strand":1,"end":140516626,"alleles":["T","C"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516628,"source":"dbSNP","strand":1,"feature_type":"variation","end":140516628,"alleles":["A","G"],"seq_region_name":"7","id":"rs1395897850","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140516629,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516629,"source":"dbSNP","seq_region_name":"7","id":"rs1167653449","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585530752","source":"dbSNP","start":140516630,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140516630,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1032004370","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516631,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140516631},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140516632,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516632,"source":"dbSNP","seq_region_name":"7","id":"rs535842331","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795705271","clinical_significance":[],"alleles":["A","G"],"end":140516633,"strand":1,"feature_type":"variation","start":140516633,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["AAA","AA"],"end":140516635,"feature_type":"variation","strand":1,"source":"dbSNP","start":140516633,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795705298","seq_region_name":"7"},{"seq_region_name":"7","id":"rs956739797","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140516634,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516634,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs988090015","source":"dbSNP","start":140516638,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140516638,"alleles":["A","C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs74598980","seq_region_name":"7","end":140516641,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140516641,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs11374146","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516642,"source":"dbSNP","strand":1,"feature_type":"variation","end":140516648,"alleles":["AAAAAAA","AAAA","AAAAAA","AAAAAAAA","AAAAAAAAA"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795705526","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516647,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140516647},{"seq_region_name":"7","id":"rs918026409","clinical_significance":[],"start":140516648,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140516648,"strand":1,"feature_type":"variation"},{"alleles":["G","A","T"],"end":140516649,"strand":1,"feature_type":"variation","start":140516649,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1176628964","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","G"],"end":140516650,"feature_type":"variation","strand":1,"source":"dbSNP","start":140516650,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs79731793","seq_region_name":"7"},{"seq_region_name":"7","id":"rs551589472","clinical_significance":[],"strand":1,"feature_type":"variation","end":140516654,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516654,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140516656,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516656,"clinical_significance":[],"seq_region_name":"7","id":"rs1585530814"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140516657,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516657,"source":"dbSNP","id":"rs546439801","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs982680848","source":"dbSNP","start":140516658,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140516658,"feature_type":"variation","strand":1},{"start":140516671,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140516671,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs926821602","clinical_significance":[]},{"source":"dbSNP","start":140516671,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["CCC","CC"],"end":140516673,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795705838"},{"seq_region_name":"7","id":"rs1585530821","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516675,"source":"dbSNP","strand":1,"feature_type":"variation","end":140516675,"alleles":["T","C"]},{"start":140516678,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140516678,"strand":1,"feature_type":"variation","id":"rs942151539","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1240092808","seq_region_name":"7","source":"dbSNP","start":140516679,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140516679,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795705970","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516681,"source":"dbSNP","strand":1,"feature_type":"variation","end":140516681,"alleles":["G","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs973718091","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516682,"feature_type":"variation","strand":1,"end":140516682,"alleles":["C","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516685,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140516685,"clinical_significance":[],"id":"rs1318981535","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1326934250","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516688,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140516688},{"strand":1,"feature_type":"variation","end":140516694,"alleles":["A","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516694,"source":"dbSNP","seq_region_name":"7","id":"rs1795706090","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140516705,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516705,"clinical_significance":[],"id":"rs1795706146","seq_region_name":"7"},{"alleles":["G","A"],"end":140516708,"strand":1,"feature_type":"variation","start":140516708,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs959591658","clinical_significance":[]},{"source":"dbSNP","start":140516710,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140516710,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795706215"},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140516713,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516713,"source":"dbSNP","seq_region_name":"7","id":"rs1391186078","clinical_significance":[]},{"end":140516715,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140516715,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795706255"},{"seq_region_name":"7","id":"rs1432688860","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516720,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140516720},{"feature_type":"variation","strand":1,"end":140516721,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516721,"clinical_significance":[],"seq_region_name":"7","id":"rs2130436540"},{"seq_region_name":"7","id":"rs571273387","clinical_significance":[],"strand":1,"feature_type":"variation","end":140516733,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516733,"source":"dbSNP"},{"start":140516734,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140516734,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs779380142","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795706371","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516735,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140516735},{"source":"dbSNP","start":140516739,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140516739,"alleles":["T","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs991180692","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1338794963","end":140516742,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140516742,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1218268427","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516746,"source":"dbSNP","strand":1,"feature_type":"variation","end":140516746,"alleles":["A","G"]},{"id":"rs919493730","seq_region_name":"7","clinical_significance":[],"start":140516753,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140516753,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1162150590","clinical_significance":[],"start":140516755,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140516755,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs755387976","end":140516757,"alleles":["CCC","CCCCC"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140516755,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516757,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140516757,"seq_region_name":"7","id":"rs1795706567","clinical_significance":[]},{"end":140516758,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","start":140516758,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs4726882","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140516766,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516766,"clinical_significance":[],"seq_region_name":"7","id":"rs941639803"},{"seq_region_name":"7","id":"rs758600709","clinical_significance":[],"end":140516767,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140516767,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1051409460","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516770,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140516770},{"clinical_significance":[],"seq_region_name":"7","id":"rs973186137","end":140516776,"alleles":["T","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140516776,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1438918807","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516777,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140516777},{"end":140516781,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140516781,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1395454567","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs576878512","alleles":["G","A"],"end":140516782,"feature_type":"variation","strand":1,"source":"dbSNP","start":140516782,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["G","A"],"end":140516784,"feature_type":"variation","strand":1,"source":"dbSNP","start":140516784,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs929197280"},{"id":"rs890101551","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516785,"source":"dbSNP","strand":1,"feature_type":"variation","end":140516785,"alleles":["C","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795707018","end":140516791,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140516791,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1252248511","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140516807,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516807,"source":"dbSNP"},{"end":140516808,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140516808,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs943111941"},{"seq_region_name":"7","id":"rs1039159485","clinical_significance":[],"alleles":["C","A"],"end":140516811,"strand":1,"feature_type":"variation","start":140516811,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140516812,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516812,"clinical_significance":[],"seq_region_name":"7","id":"rs527897361"},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140516818,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516818,"clinical_significance":[],"seq_region_name":"7","id":"rs890408402"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140516824,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516824,"clinical_significance":[],"seq_region_name":"7","id":"rs1795707329"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795707355","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516825,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140516825},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516827,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140516827,"clinical_significance":[],"seq_region_name":"7","id":"rs943303714"},{"seq_region_name":"7","id":"rs1795707417","clinical_significance":[],"start":140516830,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140516830,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140516835,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140516838,"alleles":["TCAT","TCATCAT"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1196363041"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516836,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140516836,"seq_region_name":"7","id":"rs1261491870","clinical_significance":[]},{"end":140516840,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140516840,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1232486477","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1477660243","source":"dbSNP","start":140516845,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140516845,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs2130436665","clinical_significance":[],"start":140516847,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140516847,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795707564","feature_type":"variation","strand":1,"end":140516848,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516848},{"seq_region_name":"7","id":"rs2130436676","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516852,"source":"dbSNP","strand":1,"feature_type":"variation","end":140516852,"alleles":["T","C"]},{"id":"rs1199732046","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140516853,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516853,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516855,"feature_type":"variation","strand":1,"end":140516855,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1370947420"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795707626","end":140516871,"alleles":["CACACACAC","CACACAC"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140516863,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1795707655","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140516864,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516864,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140516866,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516866,"source":"dbSNP","seq_region_name":"7","id":"rs1795707686","clinical_significance":[]},{"end":140516869,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140516869,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795707714","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140516870,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516870,"source":"dbSNP","seq_region_name":"7","id":"rs139677105","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516871,"feature_type":"variation","strand":1,"end":140516871,"alleles":["C","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795707771"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130436714","source":"dbSNP","start":140516874,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","AA"],"end":140516874,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516875,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140516875,"seq_region_name":"7","id":"rs1795707804","clinical_significance":[]},{"alleles":["C","T"],"end":140516876,"feature_type":"variation","strand":1,"source":"dbSNP","start":140516876,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795707825"},{"seq_region_name":"7","id":"rs1795707849","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516878,"source":"dbSNP","strand":1,"feature_type":"variation","end":140516881,"alleles":["AGAG","AG"]},{"start":140516879,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140516879,"strand":1,"feature_type":"variation","id":"rs893810455","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1386477269","clinical_significance":[],"strand":1,"feature_type":"variation","end":140516881,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516881,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795707963","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516882,"feature_type":"variation","strand":1,"end":140516882,"alleles":["T","G"]},{"seq_region_name":"7","id":"rs532138383","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516882,"source":"dbSNP","strand":1,"feature_type":"variation","end":140516888,"alleles":["TTTTTTT","TTTTTT"]},{"alleles":["T","A"],"end":140516883,"feature_type":"variation","strand":1,"source":"dbSNP","start":140516883,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795708046"},{"source":"dbSNP","start":140516886,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140516886,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795708108"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516888,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140516888,"seq_region_name":"7","id":"rs1795708170","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795708214","clinical_significance":[],"start":140516897,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140516897,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516901,"feature_type":"variation","strand":1,"end":140516901,"alleles":["T","G"],"clinical_significance":[],"id":"rs1795708247","seq_region_name":"7"},{"source":"dbSNP","start":140516903,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140516903,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1031617511"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563110667","feature_type":"variation","strand":1,"end":140516905,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516905},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795708344","source":"dbSNP","start":140516907,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140516907,"alleles":["G","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795708378","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516910,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140516910},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795708410","source":"dbSNP","start":140516912,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140516912,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1418685799","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516913,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140516913},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563110670","source":"dbSNP","start":140516923,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140516923,"alleles":["T","G"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140516928,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140516928,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1042510132"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585531028","feature_type":"variation","strand":1,"end":140516930,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516930},{"clinical_significance":[],"seq_region_name":"7","id":"rs891697322","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140516933,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516933},{"start":140516935,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140516935,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1175308971","clinical_significance":[]},{"start":140516936,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140516936,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795708608","clinical_significance":[]},{"seq_region_name":"7","id":"rs1452301313","clinical_significance":[],"start":140516937,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140516937,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs187954398","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140516939,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516939},{"feature_type":"variation","strand":1,"end":140516940,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516940,"clinical_significance":[],"id":"rs1193743013","seq_region_name":"7"},{"id":"rs1003735600","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516941,"source":"dbSNP","strand":1,"feature_type":"variation","end":140516941,"alleles":["G","A"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516944,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140516944,"id":"rs1795708777","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130436808","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516957,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140516957},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516961,"feature_type":"variation","strand":1,"end":140516961,"alleles":["C","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795708806"},{"seq_region_name":"7","id":"rs548023202","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516962,"source":"dbSNP","strand":1,"feature_type":"variation","end":140516962,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795708865","source":"dbSNP","start":140516963,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140516963,"feature_type":"variation","strand":1},{"id":"rs2130436822","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140516964,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516964,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1259702375","seq_region_name":"7","feature_type":"variation","strand":1,"end":140516965,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140516965},{"strand":1,"feature_type":"variation","end":140516966,"alleles":["G","C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516966,"source":"dbSNP","seq_region_name":"7","id":"rs1795708931","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs368768029","alleles":["G","A"],"end":140516972,"feature_type":"variation","strand":1,"source":"dbSNP","start":140516972,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","A","T"],"end":140516973,"strand":1,"feature_type":"variation","start":140516973,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1421428421","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516974,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140516974,"seq_region_name":"7","id":"rs1296206107","clinical_significance":[]},{"id":"rs1585531052","seq_region_name":"7","clinical_significance":[],"start":140516980,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140516980,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795709120","end":140516981,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140516981,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1035583472","clinical_significance":[],"strand":1,"feature_type":"variation","end":140516988,"alleles":["A","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516988,"source":"dbSNP"},{"start":140516990,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140516990,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130436845","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516993,"source":"dbSNP","strand":1,"feature_type":"variation","end":140516993,"alleles":["T","C"],"id":"rs1795709203","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1209181148","alleles":["C","A","G"],"end":140516994,"feature_type":"variation","strand":1,"source":"dbSNP","start":140516994,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140516998,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140516998,"source":"dbSNP","seq_region_name":"7","id":"rs970670091","clinical_significance":[]},{"seq_region_name":"7","id":"rs1339602267","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517000,"source":"dbSNP","strand":1,"feature_type":"variation","end":140517000,"alleles":["A","G","T"]},{"seq_region_name":"7","id":"rs116041451","clinical_significance":[],"strand":1,"feature_type":"variation","end":140517002,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517002,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1795709307","seq_region_name":"7","source":"dbSNP","start":140517003,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140517003,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140517004,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517004,"source":"dbSNP","seq_region_name":"7","id":"rs1284220703","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795709374","clinical_significance":[],"strand":1,"feature_type":"variation","end":140517008,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517008,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795709400","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517010,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140517010},{"source":"dbSNP","start":140517014,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140517014,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1333018531"},{"source":"dbSNP","start":140517015,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140517015,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1012508628"},{"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140517017,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517017,"clinical_significance":[],"seq_region_name":"7","id":"rs150026869"},{"start":140517018,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C"],"end":140517018,"strand":1,"feature_type":"variation","id":"rs1795709536","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs527549142","seq_region_name":"7","feature_type":"variation","strand":1,"end":140517020,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517020},{"seq_region_name":"7","id":"rs1432649511","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140517023,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517023,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140517024,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517024,"source":"dbSNP","id":"rs963611177","seq_region_name":"7","clinical_significance":[]},{"id":"rs552358889","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517025,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140517025},{"alleles":["A","-"],"end":140517026,"strand":1,"feature_type":"variation","start":140517026,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs919036923","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140517028,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517028,"source":"dbSNP","seq_region_name":"7","id":"rs1371217285","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1193077849","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140517029,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517029},{"seq_region_name":"7","id":"rs1795709950","clinical_significance":[],"end":140517031,"alleles":["CCC","CC"],"strand":1,"feature_type":"variation","start":140517029,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1652330908","alleles":["C","T"],"end":140517030,"feature_type":"variation","strand":1,"source":"dbSNP","start":140517030,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517031,"feature_type":"variation","strand":1,"end":140517031,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs144339608"},{"clinical_significance":[],"id":"rs1284451087","seq_region_name":"7","source":"dbSNP","start":140517032,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140517032,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs768927603","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517033,"feature_type":"variation","strand":1,"end":140517033,"alleles":["G","C"]},{"strand":1,"feature_type":"variation","end":140517055,"alleles":["TAAGTTTTTCTTGTATTTTTA","TA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517035,"source":"dbSNP","id":"rs1795710077","seq_region_name":"7","clinical_significance":[]},{"id":"rs911745353","seq_region_name":"7","clinical_significance":[],"alleles":["AA","-"],"end":140517037,"strand":1,"feature_type":"variation","start":140517036,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795710131","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140517042,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517042,"source":"dbSNP"},{"seq_region_name":"7","id":"rs773271140","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517050,"source":"dbSNP","strand":1,"feature_type":"variation","end":140517050,"alleles":["T","G"]},{"strand":1,"feature_type":"variation","end":140517054,"alleles":["TTTTT","TTTT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517050,"source":"dbSNP","id":"rs1795710193","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140517051,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517051,"source":"dbSNP","id":"rs1795710230","seq_region_name":"7","clinical_significance":[]},{"end":140517059,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140517059,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795710257","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140517060,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517060,"clinical_significance":[],"seq_region_name":"7","id":"rs1585531098"},{"clinical_significance":[],"id":"rs549589348","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140517063,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517063},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795710330","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517065,"feature_type":"variation","strand":1,"end":140517065,"alleles":["G","T"]},{"clinical_significance":[],"id":"rs1274115585","seq_region_name":"7","alleles":["G","T"],"end":140517066,"feature_type":"variation","strand":1,"source":"dbSNP","start":140517066,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1795710379","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517070,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140517070},{"id":"rs1795710407","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517071,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140517071},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517072,"feature_type":"variation","strand":1,"alleles":["G","GG"],"end":140517072,"clinical_significance":[],"id":"rs1223662425","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1338045696","end":140517073,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140517073,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517075,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140517075,"seq_region_name":"7","id":"rs866405290","clinical_significance":[]},{"end":140517076,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140517076,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1217491188"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517077,"feature_type":"variation","strand":1,"end":140517077,"alleles":["G","A"],"clinical_significance":[],"id":"rs1795710591","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517081,"feature_type":"variation","strand":1,"end":140517081,"alleles":["G","C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs987692673"},{"alleles":["C","T"],"end":140517082,"strand":1,"feature_type":"variation","start":140517082,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1294812933","clinical_significance":[]},{"clinical_significance":[],"id":"rs1412499515","seq_region_name":"7","alleles":["G","A"],"end":140517085,"feature_type":"variation","strand":1,"source":"dbSNP","start":140517085,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1795710663","seq_region_name":"7","clinical_significance":[],"start":140517086,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140517086,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517088,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140517088,"seq_region_name":"7","id":"rs1431095706","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517090,"feature_type":"variation","strand":1,"end":140517090,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795710726"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130437018","source":"dbSNP","start":140517091,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140517091,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1585531156","seq_region_name":"7","end":140517097,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140517097,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140517109,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140517109,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1339704176","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517111,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140517111,"seq_region_name":"7","id":"rs1197616013","clinical_significance":[]},{"alleles":["A","G"],"end":140517114,"feature_type":"variation","strand":1,"source":"dbSNP","start":140517114,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs776743146","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1795710885","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517115,"feature_type":"variation","strand":1,"end":140517115,"alleles":["T","C"]},{"clinical_significance":[],"id":"rs538044199","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140517116,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517116},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795710939","end":140517117,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140517117,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1585531169","seq_region_name":"7","clinical_significance":[],"start":140517118,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140517118,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"end":140517129,"alleles":["CCTGCCTGCCT","CCTGCCTGCCTGCCT"],"strand":1,"feature_type":"variation","start":140517119,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1363894036","clinical_significance":[]},{"seq_region_name":"7","id":"rs1563110745","clinical_significance":[],"alleles":["G","T"],"end":140517122,"strand":1,"feature_type":"variation","start":140517122,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585531175","alleles":["C","T"],"end":140517124,"feature_type":"variation","strand":1,"source":"dbSNP","start":140517124,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1394253466","feature_type":"variation","strand":1,"alleles":["GCCTTGGCCT","GCCTTGGCCTTGGCCT"],"end":140517135,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517126},{"end":140517128,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140517128,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795711109","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1440931390","feature_type":"variation","strand":1,"end":140517130,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517130},{"source":"dbSNP","start":140517133,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140517133,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs191892447"},{"source":"dbSNP","start":140517135,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140517135,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795711187"},{"alleles":["T","G"],"end":140517137,"feature_type":"variation","strand":1,"source":"dbSNP","start":140517137,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795711216"},{"clinical_significance":[],"seq_region_name":"7","id":"rs915149997","end":140517145,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140517145,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1462085283","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517146,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140517146},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140517148,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517148,"source":"dbSNP","seq_region_name":"7","id":"rs1156812432","clinical_significance":[]},{"id":"rs568554183","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517149,"source":"dbSNP","strand":1,"feature_type":"variation","end":140517149,"alleles":["G","A"]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140517154,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517154,"source":"dbSNP","seq_region_name":"7","id":"rs1795711343","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795711374","clinical_significance":[],"end":140517155,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140517155,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs946758457","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140517156,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517156,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795711434","source":"dbSNP","start":140517158,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140517158,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1163101590","source":"dbSNP","start":140517160,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140517160,"alleles":["T","-"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140517161,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517161,"source":"dbSNP","id":"rs1795711486","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140517164,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517164,"clinical_significance":[],"seq_region_name":"7","id":"rs1795711508"},{"source":"dbSNP","start":140517170,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140517170,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs566149750","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517171,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140517171,"seq_region_name":"7","id":"rs1042760654","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1184466999","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517172,"feature_type":"variation","strand":1,"end":140517172,"alleles":["C","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517174,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140517174,"id":"rs535880755","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs554178944","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140517175,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517175},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140517176,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517176,"source":"dbSNP","seq_region_name":"7","id":"rs904257701","clinical_significance":[]},{"source":"dbSNP","start":140517178,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["CAGGCAGG","CAGG"],"end":140517185,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1385324031"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517179,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140517179,"clinical_significance":[],"seq_region_name":"7","id":"rs1274479471"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795711763","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517181,"feature_type":"variation","strand":1,"end":140517181,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795711789","source":"dbSNP","start":140517183,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140517183,"alleles":["A","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795711819","source":"dbSNP","start":140517185,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140517185,"alleles":["G","A"],"feature_type":"variation","strand":1},{"start":140517186,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140517186,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585531244","clinical_significance":[]},{"source":"dbSNP","start":140517189,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140517189,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795711870"},{"alleles":["T","A"],"end":140517194,"feature_type":"variation","strand":1,"source":"dbSNP","start":140517194,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795711906"},{"seq_region_name":"7","id":"rs1056527922","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517196,"source":"dbSNP","strand":1,"feature_type":"variation","end":140517196,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs2130437167","clinical_significance":[],"strand":1,"feature_type":"variation","end":140517207,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517207,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1280649086","seq_region_name":"7","source":"dbSNP","start":140517211,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140517211,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs935871573","clinical_significance":[],"end":140517214,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140517214,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517219,"feature_type":"variation","strand":1,"end":140517219,"alleles":["C","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs749289927"},{"id":"rs1355242722","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140517223,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517223,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1323064839","clinical_significance":[],"start":140517224,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G","T"],"end":140517224,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1336460159","source":"dbSNP","start":140517225,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140517225,"alleles":["G","C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795712167","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140517231,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517231},{"seq_region_name":"7","id":"rs1795712208","clinical_significance":[],"strand":1,"feature_type":"variation","end":140517236,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517236,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517239,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140517239,"seq_region_name":"7","id":"rs1242343519","clinical_significance":[]},{"alleles":["G","T"],"end":140517241,"feature_type":"variation","strand":1,"source":"dbSNP","start":140517241,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1053379637","seq_region_name":"7"},{"start":140517247,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140517247,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs572790900","clinical_significance":[]},{"start":140517250,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140517250,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs567502124","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130437213","source":"dbSNP","start":140517253,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140517253,"alleles":["G","A"],"feature_type":"variation","strand":1},{"alleles":["A","C"],"end":140517255,"feature_type":"variation","strand":1,"source":"dbSNP","start":140517255,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795712326","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140517258,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517258,"clinical_significance":[],"seq_region_name":"7","id":"rs540096094"},{"source":"dbSNP","start":140517262,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140517262,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1441508333","seq_region_name":"7"},{"clinical_significance":[],"id":"rs372212962","seq_region_name":"7","alleles":["C","G","T"],"end":140517263,"feature_type":"variation","strand":1,"source":"dbSNP","start":140517263,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1017239369","alleles":["C","T"],"end":140517265,"feature_type":"variation","strand":1,"source":"dbSNP","start":140517265,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1014131859","source":"dbSNP","start":140517271,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140517271,"alleles":["A","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1247257915","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517273,"feature_type":"variation","strand":1,"end":140517273,"alleles":["G","A","C"]},{"seq_region_name":"7","id":"rs1160461248","clinical_significance":[],"alleles":["A","G"],"end":140517275,"strand":1,"feature_type":"variation","start":140517275,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795712609","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140517278,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517278},{"seq_region_name":"7","id":"rs1468966849","clinical_significance":[],"start":140517279,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140517279,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1795712676","clinical_significance":[],"alleles":["C","T"],"end":140517285,"strand":1,"feature_type":"variation","start":140517285,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1380037096","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517287,"feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140517287},{"id":"rs1795712765","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517294,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140517294},{"clinical_significance":[],"id":"rs1194871932","seq_region_name":"7","alleles":["C","A"],"end":140517302,"feature_type":"variation","strand":1,"source":"dbSNP","start":140517302,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs2130437269","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517305,"source":"dbSNP","strand":1,"feature_type":"variation","end":140517306,"alleles":["GG","G"]},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140517306,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517306,"source":"dbSNP","seq_region_name":"7","id":"rs1024135124","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs962939563","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517310,"feature_type":"variation","strand":1,"end":140517310,"alleles":["G","A","C"]},{"id":"rs1218784314","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140517312,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517312,"source":"dbSNP"},{"alleles":["G","A"],"end":140517313,"feature_type":"variation","strand":1,"source":"dbSNP","start":140517313,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1208878792"},{"source":"dbSNP","start":140517314,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140517314,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1450490967","seq_region_name":"7"},{"end":140517315,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140517315,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795712994","clinical_significance":[]},{"clinical_significance":[],"id":"rs2130437292","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517317,"feature_type":"variation","strand":1,"end":140517317,"alleles":["G","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs994541606","source":"dbSNP","start":140517318,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140517318,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795713059","end":140517324,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140517324,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["A","G"],"end":140517326,"feature_type":"variation","strand":1,"source":"dbSNP","start":140517326,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795713087"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517327,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140517327,"clinical_significance":[],"seq_region_name":"7","id":"rs1026413118"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1351318404","feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140517328,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517328},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795713178","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517329,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140517329},{"feature_type":"variation","strand":1,"end":140517330,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517330,"clinical_significance":[],"id":"rs1250746801","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1271462398","clinical_significance":[],"end":140517331,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140517331,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140517332,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517332,"clinical_significance":[],"seq_region_name":"7","id":"rs1795713268"},{"source":"dbSNP","start":140517333,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140517333,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1458732668"},{"alleles":["A","G"],"end":140517335,"strand":1,"feature_type":"variation","start":140517335,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs906585678","clinical_significance":[]},{"seq_region_name":"7","id":"rs770601427","clinical_significance":[],"start":140517336,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140517336,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs950390613","clinical_significance":[],"strand":1,"feature_type":"variation","end":140517347,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517347,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1435873778","clinical_significance":[],"end":140517351,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140517351,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517353,"feature_type":"variation","strand":1,"end":140517353,"alleles":["T","A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs558333853"},{"start":140517359,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140517359,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1320574507","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517359,"source":"dbSNP","strand":1,"feature_type":"variation","end":140517362,"alleles":["CCCC","CCC"],"seq_region_name":"7","id":"rs2130437333","clinical_significance":[]},{"id":"rs987631546","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140517360,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517360,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795713557","clinical_significance":[],"alleles":["C","T"],"end":140517362,"strand":1,"feature_type":"variation","start":140517362,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140517364,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140517364,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1033799871","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140517373,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517373,"source":"dbSNP","seq_region_name":"7","id":"rs1795713614","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs911606414","end":140517374,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140517374,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140517378,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517378,"source":"dbSNP","seq_region_name":"7","id":"rs1174665345","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795713695","source":"dbSNP","start":140517380,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140517380,"feature_type":"variation","strand":1},{"end":140517381,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140517381,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs964547348","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130437358","end":140517386,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140517386,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs963774721","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517387,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140517387},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517389,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140517389,"clinical_significance":[],"id":"rs1477432631","seq_region_name":"7"},{"id":"rs1166758707","seq_region_name":"7","clinical_significance":[],"end":140517390,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140517390,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1217571296","clinical_significance":[],"strand":1,"feature_type":"variation","end":140517394,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517394,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563110864","feature_type":"variation","strand":1,"end":140517395,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517395},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795714015","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140517396,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517396},{"alleles":["C","T"],"end":140517397,"strand":1,"feature_type":"variation","start":140517397,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs576605369","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795714069","clinical_significance":[],"alleles":["C","G"],"end":140517405,"strand":1,"feature_type":"variation","start":140517405,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1284781383","end":140517406,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140517406,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140517407,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517407,"clinical_significance":[],"seq_region_name":"7","id":"rs946610365"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517408,"source":"dbSNP","strand":1,"feature_type":"variation","end":140517408,"alleles":["G","A"],"seq_region_name":"7","id":"rs1795714160","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1349720106","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140517413,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517413},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140517418,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517418,"clinical_significance":[],"id":"rs1795714213","seq_region_name":"7"},{"end":140517420,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140517420,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1276473028"},{"clinical_significance":[],"id":"rs1218539155","seq_region_name":"7","alleles":["C","G"],"end":140517429,"feature_type":"variation","strand":1,"source":"dbSNP","start":140517429,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1026498811","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140517433,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517433},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140517434,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517434,"clinical_significance":[],"seq_region_name":"7","id":"rs374794631"},{"id":"rs1457183284","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140517435,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517435,"source":"dbSNP"},{"source":"dbSNP","start":140517439,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140517439,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs923954675"},{"end":140517441,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140517441,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130437418","clinical_significance":[]},{"seq_region_name":"7","id":"rs1398158987","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517442,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140517442},{"id":"rs1795714466","seq_region_name":"7","clinical_significance":[],"start":140517443,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140517443,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs11981557","clinical_significance":[],"alleles":["G","A"],"end":140517444,"strand":1,"feature_type":"variation","start":140517444,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1795714566","seq_region_name":"7","end":140517445,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140517445,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140517447,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517447,"clinical_significance":[],"seq_region_name":"7","id":"rs1795714600"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795714628","feature_type":"variation","strand":1,"alleles":["T","-"],"end":140517450,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517450},{"clinical_significance":[],"seq_region_name":"7","id":"rs1313664580","alleles":["C","T"],"end":140517451,"feature_type":"variation","strand":1,"source":"dbSNP","start":140517451,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140517455,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140517455,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1437025797"},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140517459,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517459,"source":"dbSNP","seq_region_name":"7","id":"rs1373996108","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795714752","seq_region_name":"7","feature_type":"variation","strand":1,"end":140517463,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517463},{"seq_region_name":"7","id":"rs1056597316","clinical_significance":[],"end":140517464,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140517464,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1401276902","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140517469,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517469,"source":"dbSNP"},{"alleles":["G","A"],"end":140517470,"strand":1,"feature_type":"variation","start":140517470,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1422199148","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140517471,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517471,"clinical_significance":[],"seq_region_name":"7","id":"rs1449142702"},{"seq_region_name":"7","id":"rs987725316","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517472,"source":"dbSNP","strand":1,"feature_type":"variation","end":140517472,"alleles":["C","T"]},{"source":"dbSNP","start":140517474,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140517474,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795714939"},{"end":140517476,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140517476,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795714961"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795714998","source":"dbSNP","start":140517481,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140517481,"alleles":["C","T"],"feature_type":"variation","strand":1},{"id":"rs1795715019","seq_region_name":"7","clinical_significance":[],"start":140517483,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140517483,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140517485,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517485,"source":"dbSNP","seq_region_name":"7","id":"rs2130437466","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140517489,"alleles":["TGTGT","TGT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517485,"clinical_significance":[],"id":"rs1795715047","seq_region_name":"7"},{"source":"dbSNP","start":140517486,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140517486,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1476531346"},{"alleles":["G","A"],"end":140517488,"strand":1,"feature_type":"variation","start":140517488,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795715106","clinical_significance":[]},{"source":"dbSNP","start":140517492,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140517492,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1376886576"},{"alleles":["G","T"],"end":140517494,"strand":1,"feature_type":"variation","start":140517494,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795715160","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140517498,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517498,"clinical_significance":[],"seq_region_name":"7","id":"rs1795715184"},{"clinical_significance":[],"seq_region_name":"7","id":"rs372884999","source":"dbSNP","start":140517502,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140517502,"alleles":["C","G","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795715244","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517502,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CGCTGGTGAGAGCTGAGGGC","CGCTGGTGAGAGCTGAGGGCCGCTGGTGAGAGCTGAGGGC"],"end":140517521},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517503,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140517503,"seq_region_name":"7","id":"rs1486550752","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130437490","clinical_significance":[],"strand":1,"feature_type":"variation","end":140517509,"alleles":["TGGTG","TG"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517505,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1254017877","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517506,"feature_type":"variation","strand":1,"end":140517507,"alleles":["GG","G"]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140517510,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517510,"clinical_significance":[],"seq_region_name":"7","id":"rs574168220"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517511,"source":"dbSNP","strand":1,"feature_type":"variation","end":140517511,"alleles":["G","C"],"seq_region_name":"7","id":"rs964436541","clinical_significance":[]},{"seq_region_name":"7","id":"rs1308013275","clinical_significance":[],"alleles":["G","A"],"end":140517520,"strand":1,"feature_type":"variation","start":140517520,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140517521,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140517521,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795715414"},{"clinical_significance":[],"seq_region_name":"7","id":"rs974794828","source":"dbSNP","start":140517525,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140517525,"feature_type":"variation","strand":1},{"id":"rs1320330225","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140517527,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517527,"source":"dbSNP"},{"id":"rs1795715498","seq_region_name":"7","clinical_significance":[],"start":140517529,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","-"],"end":140517529,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1274982548","clinical_significance":[],"strand":1,"feature_type":"variation","end":140517531,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517531,"source":"dbSNP"},{"end":140517535,"alleles":["T","TT"],"strand":1,"feature_type":"variation","start":140517535,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs898636824","clinical_significance":[]},{"source":"dbSNP","start":140517535,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140517535,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795715545"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140517536,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517536,"source":"dbSNP","seq_region_name":"7","id":"rs1795715591","clinical_significance":[]},{"alleles":["T","A"],"end":140517538,"feature_type":"variation","strand":1,"source":"dbSNP","start":140517538,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130437536"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795715611","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517541,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140517541},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130437544","alleles":["C","T"],"end":140517542,"feature_type":"variation","strand":1,"source":"dbSNP","start":140517542,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517543,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140517543,"seq_region_name":"7","id":"rs1317353535","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517544,"feature_type":"variation","strand":1,"end":140517544,"alleles":["T","C"],"clinical_significance":[],"id":"rs1244459883","seq_region_name":"7"},{"seq_region_name":"7","id":"rs994845664","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517548,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140517548},{"start":140517552,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140517552,"alleles":["G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1416852609","clinical_significance":[]},{"clinical_significance":[],"id":"rs1377511743","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517553,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140517553},{"clinical_significance":[],"seq_region_name":"7","id":"rs925616621","end":140517559,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140517559,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140517560,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517560,"source":"dbSNP","id":"rs935761654","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140517561,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517561,"source":"dbSNP","seq_region_name":"7","id":"rs1585531574","clinical_significance":[]},{"seq_region_name":"7","id":"rs1356821941","clinical_significance":[],"end":140517563,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140517563,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517566,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140517566,"clinical_significance":[],"seq_region_name":"7","id":"rs1168888511"},{"end":140517569,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140517569,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs775815210"},{"alleles":["A","C","G"],"end":140517570,"strand":1,"feature_type":"variation","start":140517570,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795715954","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795715984","clinical_significance":[],"start":140517572,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140517572,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517579,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140517579,"seq_region_name":"7","id":"rs1052767947","clinical_significance":[]},{"seq_region_name":"7","id":"rs1319548697","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517580,"source":"dbSNP","strand":1,"feature_type":"variation","end":140517580,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1795716079","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517584,"source":"dbSNP","strand":1,"feature_type":"variation","end":140517584,"alleles":["C","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517587,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140517587,"clinical_significance":[],"id":"rs1795716109","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1422243463","alleles":["T","C"],"end":140517588,"feature_type":"variation","strand":1,"source":"dbSNP","start":140517588,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795716154","source":"dbSNP","start":140517589,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140517589,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1165276048","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517592,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140517592},{"feature_type":"variation","strand":1,"end":140517593,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517593,"clinical_significance":[],"seq_region_name":"7","id":"rs913066957"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795716338","feature_type":"variation","strand":1,"alleles":["TCCCCGCTGTCCCTGCTGTCCCC","TCCCCGCTGTCCCTGCTGTCCCCGCTGTCCCTGCTGTCCCC"],"end":140517617,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517595},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140517596,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517596,"source":"dbSNP","seq_region_name":"7","id":"rs1795716363","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517597,"source":"dbSNP","strand":1,"feature_type":"variation","end":140517597,"alleles":["C","T"],"seq_region_name":"7","id":"rs1795716396","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517599,"source":"dbSNP","strand":1,"feature_type":"variation","end":140517599,"alleles":["C","T"],"seq_region_name":"7","id":"rs541441268","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs771697503","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517600,"feature_type":"variation","strand":1,"end":140517600,"alleles":["G","A"]},{"end":140517601,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140517601,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795716493"},{"end":140517603,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140517603,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795716519","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140517604,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517604,"source":"dbSNP","seq_region_name":"7","id":"rs886111208","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795716582","clinical_significance":[],"start":140517609,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["GCTGTCCCC","GCTGTCCCCGCTGTCCCC"],"end":140517617,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140517610,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140517610,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs775125954"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517613,"feature_type":"variation","strand":1,"end":140517613,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795716645"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517614,"feature_type":"variation","strand":1,"end":140517614,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795716674"},{"clinical_significance":[],"seq_region_name":"7","id":"rs559678984","source":"dbSNP","start":140517618,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140517618,"alleles":["A","G"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140517619,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517619,"clinical_significance":[],"seq_region_name":"7","id":"rs1480810624"},{"id":"rs1795716758","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140517623,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517623,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517626,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140517626,"seq_region_name":"7","id":"rs527584321","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140517627,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517627,"source":"dbSNP","id":"rs1196644965","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517634,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140517634,"clinical_significance":[],"id":"rs552238599","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140517636,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517636,"source":"dbSNP","seq_region_name":"7","id":"rs564399730","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517638,"source":"dbSNP","strand":1,"feature_type":"variation","end":140517638,"alleles":["G","A"],"seq_region_name":"7","id":"rs1170845442","clinical_significance":[]},{"clinical_significance":[],"id":"rs531442082","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517641,"feature_type":"variation","strand":1,"end":140517641,"alleles":["C","G"]},{"feature_type":"variation","strand":1,"end":140517648,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517648,"clinical_significance":[],"seq_region_name":"7","id":"rs1320146951"},{"seq_region_name":"7","id":"rs549928293","clinical_significance":[],"alleles":["G","A","T"],"end":140517649,"strand":1,"feature_type":"variation","start":140517649,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130437677","source":"dbSNP","start":140517651,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140517651,"feature_type":"variation","strand":1},{"alleles":["C","T"],"end":140517652,"feature_type":"variation","strand":1,"source":"dbSNP","start":140517652,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs899138162"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1168722610","source":"dbSNP","start":140517654,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140517654,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["TTTTT","TTTTTT"],"end":140517662,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517658,"clinical_significance":[],"id":"rs1795717130","seq_region_name":"7"},{"seq_region_name":"7","id":"rs2130437691","clinical_significance":[],"start":140517663,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140517663,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1795717151","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517664,"source":"dbSNP","strand":1,"feature_type":"variation","end":140517664,"alleles":["G","A"]},{"clinical_significance":[],"id":"rs1375951668","seq_region_name":"7","source":"dbSNP","start":140517666,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140517666,"alleles":["C","G"],"feature_type":"variation","strand":1},{"alleles":["C","-"],"end":140517669,"strand":1,"feature_type":"variation","start":140517669,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795717227","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130437701","source":"dbSNP","start":140517669,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140517669,"alleles":["C","T"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140517669,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["CTCC","C"],"end":140517672,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs974574149"},{"start":140517675,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140517675,"alleles":["A","C"],"strand":1,"feature_type":"variation","id":"rs1585531655","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140517676,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517676,"clinical_significance":[],"seq_region_name":"7","id":"rs967883359"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517676,"source":"dbSNP","strand":1,"feature_type":"variation","end":140517678,"alleles":["CCC","CC"],"id":"rs1022095199","seq_region_name":"7","clinical_significance":[]},{"id":"rs1326007996","seq_region_name":"7","clinical_significance":[],"end":140517680,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140517680,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140517681,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140517681,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795717427"},{"strand":1,"feature_type":"variation","end":140517682,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517682,"source":"dbSNP","seq_region_name":"7","id":"rs1458960952","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795717473","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140517684,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517684},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585531683","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517684,"feature_type":"variation","strand":1,"end":140517708,"alleles":["GCTTCTGGTCCAGAAAACGCAAGCT","GCT"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795717537","feature_type":"variation","strand":1,"end":140517685,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517685},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517686,"feature_type":"variation","strand":1,"end":140517686,"alleles":["T","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1399654216"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795717601","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140517696,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517696},{"seq_region_name":"7","id":"rs1795717635","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517697,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AAAA","AAAAA"],"end":140517700},{"feature_type":"variation","strand":1,"end":140517698,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517698,"clinical_significance":[],"seq_region_name":"7","id":"rs1366378922"},{"start":140517701,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140517701,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","id":"rs760173150","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795717748","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517702,"feature_type":"variation","strand":1,"end":140517702,"alleles":["G","A"]},{"start":140517706,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140517706,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs995339182","clinical_significance":[]},{"source":"dbSNP","start":140517708,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140517708,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795717802","seq_region_name":"7"},{"id":"rs1409885456","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140517710,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517710,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795717864","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517711,"source":"dbSNP","strand":1,"feature_type":"variation","end":140517716,"alleles":["CTCTCT","CTCT"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1026363438","alleles":["C","T"],"end":140517713,"feature_type":"variation","strand":1,"source":"dbSNP","start":140517713,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1176765525","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["CTCTGGCTGC","C"],"end":140517722,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517713},{"seq_region_name":"7","id":"rs1253474697","clinical_significance":[],"alleles":["T","C"],"end":140517714,"strand":1,"feature_type":"variation","start":140517714,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795717965","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517723,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140517723},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517724,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140517724,"seq_region_name":"7","id":"rs1585531708","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795718012","seq_region_name":"7","source":"dbSNP","start":140517726,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140517726,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs763649946","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517727,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140517727},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517731,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","G"],"end":140517731,"seq_region_name":"7","id":"rs115551420","clinical_significance":[]},{"alleles":["C","T"],"end":140517736,"strand":1,"feature_type":"variation","start":140517736,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1009056119","clinical_significance":[]},{"seq_region_name":"7","id":"rs1377595343","clinical_significance":[],"end":140517736,"alleles":["C","-"],"strand":1,"feature_type":"variation","start":140517736,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs529370700","alleles":["G","A","C"],"end":140517737,"feature_type":"variation","strand":1,"source":"dbSNP","start":140517737,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs965349350","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517739,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140517739},{"clinical_significance":[],"seq_region_name":"7","id":"rs375183887","alleles":["G","A"],"end":140517740,"feature_type":"variation","strand":1,"source":"dbSNP","start":140517740,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140517741,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140517741,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795718300"},{"seq_region_name":"7","id":"rs974993271","clinical_significance":[],"start":140517742,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140517742,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1319173662","clinical_significance":[],"end":140517743,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140517743,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1307510543","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517745,"source":"dbSNP","strand":1,"feature_type":"variation","end":140517745,"alleles":["A","C"]},{"end":140517746,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140517746,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1239797857","clinical_significance":[]},{"id":"rs1342702679","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140517747,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517747,"source":"dbSNP"},{"end":140517748,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140517748,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs547819846","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585531754","alleles":["A","C"],"end":140517754,"feature_type":"variation","strand":1,"source":"dbSNP","start":140517754,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs762419478","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517755,"feature_type":"variation","strand":1,"end":140517755,"alleles":["C","A","T"]},{"seq_region_name":"7","id":"rs1306214510","clinical_significance":[],"start":140517757,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140517757,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140517759,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517759,"source":"dbSNP","id":"rs1795718609","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1388061812","end":140517766,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140517766,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1585531772","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140517769,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517769},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795718703","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517770,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140517770},{"seq_region_name":"7","id":"rs1795718731","clinical_significance":[],"start":140517771,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140517771,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140517772,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517772,"source":"dbSNP","seq_region_name":"7","id":"rs1323650562","clinical_significance":[]},{"start":140517778,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G","T"],"end":140517778,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs566029898","clinical_significance":[]},{"seq_region_name":"7","id":"rs1211588019","clinical_significance":[],"start":140517779,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140517779,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"end":140517781,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140517781,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585531784"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1453986525","end":140517783,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140517783,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795718910","end":140517785,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140517785,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795718937","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517786,"feature_type":"variation","strand":1,"end":140517786,"alleles":["G","C"]},{"seq_region_name":"7","id":"rs912978375","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517788,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140517788},{"feature_type":"variation","strand":1,"end":140517793,"alleles":["CCCCCC","CCCCC","CCCCCCC"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517788,"clinical_significance":[],"seq_region_name":"7","id":"rs1585531792"},{"source":"dbSNP","start":140517789,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140517789,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795719041"},{"seq_region_name":"7","id":"rs949917771","clinical_significance":[],"end":140517791,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140517791,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs35195849","seq_region_name":"7","feature_type":"variation","strand":1,"end":140517793,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517793},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517794,"source":"dbSNP","strand":1,"feature_type":"variation","end":140517794,"alleles":["G","A"],"seq_region_name":"7","id":"rs1795719197","clinical_significance":[]},{"seq_region_name":"7","id":"rs927126952","clinical_significance":[],"alleles":["C","A","T"],"end":140517795,"strand":1,"feature_type":"variation","start":140517795,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517795,"feature_type":"variation","strand":1,"alleles":["CCCCCC","CCCCC"],"end":140517800,"clinical_significance":[],"id":"rs1438806398","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517798,"feature_type":"variation","strand":1,"end":140517798,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1482884671"},{"seq_region_name":"7","id":"rs188965081","clinical_significance":[],"start":140517799,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140517799,"alleles":["C","A","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs369789663","seq_region_name":"7","feature_type":"variation","strand":1,"end":140517800,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517800},{"seq_region_name":"7","id":"rs1585531816","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517801,"source":"dbSNP","strand":1,"feature_type":"variation","end":140517801,"alleles":["A","C"]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140517803,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517803,"clinical_significance":[],"seq_region_name":"7","id":"rs1266752273"},{"seq_region_name":"7","id":"rs1038256852","clinical_significance":[],"alleles":["T","G"],"end":140517805,"strand":1,"feature_type":"variation","start":140517805,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563111015","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140517806,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517806},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517808,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140517808,"clinical_significance":[],"seq_region_name":"7","id":"rs1795719545"},{"end":140517821,"alleles":["ACAGGCAGTGCACA","ACA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140517808,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795719568"},{"id":"rs948133993","seq_region_name":"7","clinical_significance":[],"start":140517809,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140517809,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140517811,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517811,"source":"dbSNP","id":"rs899163845","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140517814,"alleles":["A","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517814,"source":"dbSNP","seq_region_name":"7","id":"rs994836552","clinical_significance":[]},{"source":"dbSNP","start":140517818,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140517818,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795719694"},{"seq_region_name":"7","id":"rs1476681566","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140517821,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517821,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1795719736","seq_region_name":"7","feature_type":"variation","strand":1,"end":140517826,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517826},{"end":140517833,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140517833,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs898664878","clinical_significance":[]},{"start":140517839,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140517839,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795719798","clinical_significance":[]},{"alleles":["G","A"],"end":140517842,"feature_type":"variation","strand":1,"source":"dbSNP","start":140517842,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1563111030","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140517849,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517849,"clinical_significance":[],"id":"rs181652216","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517850,"source":"dbSNP","strand":1,"feature_type":"variation","end":140517850,"alleles":["C","G","T"],"seq_region_name":"7","id":"rs1349023794","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517853,"feature_type":"variation","strand":1,"end":140517853,"alleles":["C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795719904"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795719942","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140517854,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517854},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517856,"source":"dbSNP","strand":1,"feature_type":"variation","end":140517856,"alleles":["G","A"],"id":"rs1795719979","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795720022","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140517863,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517863},{"alleles":["T","C"],"end":140517864,"strand":1,"feature_type":"variation","start":140517864,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1231705205","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795720093","seq_region_name":"7","source":"dbSNP","start":140517867,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140517867,"alleles":["G","A","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1047871269","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517869,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140517869},{"strand":1,"feature_type":"variation","end":140517870,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517870,"source":"dbSNP","seq_region_name":"7","id":"rs3748088","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1047794824","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517871,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140517871},{"clinical_significance":[],"seq_region_name":"7","id":"rs3748089","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517874,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140517874},{"clinical_significance":[],"seq_region_name":"7","id":"rs1342024146","feature_type":"variation","strand":1,"end":140517874,"alleles":["-","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517875},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517875,"source":"dbSNP","strand":1,"feature_type":"variation","end":140517875,"alleles":["T","C"],"seq_region_name":"7","id":"rs1423127636","clinical_significance":[]},{"seq_region_name":"7","id":"rs574205483","clinical_significance":[],"alleles":["C","T"],"end":140517876,"strand":1,"feature_type":"variation","start":140517876,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517877,"source":"dbSNP","strand":1,"feature_type":"variation","end":140517877,"alleles":["A","G"],"id":"rs1008538616","seq_region_name":"7","clinical_significance":[]},{"start":140517879,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140517879,"alleles":["A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1018549287","clinical_significance":[]},{"id":"rs1795720547","seq_region_name":"7","clinical_significance":[],"end":140517881,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140517881,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1464470260","seq_region_name":"7","source":"dbSNP","start":140517883,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140517883,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795720606","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517886,"feature_type":"variation","strand":1,"end":140517886,"alleles":["G","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1178316404","alleles":["T","A"],"end":140517888,"feature_type":"variation","strand":1,"source":"dbSNP","start":140517888,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795720632","clinical_significance":[],"alleles":["A","C"],"end":140517889,"strand":1,"feature_type":"variation","start":140517889,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140517890,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517890,"clinical_significance":[],"seq_region_name":"7","id":"rs1795720666"},{"clinical_significance":[],"id":"rs185374571","seq_region_name":"7","source":"dbSNP","start":140517894,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C","G"],"end":140517894,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs79755811","end":140517895,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140517895,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140517902,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517902,"source":"dbSNP","seq_region_name":"7","id":"rs553448162","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517905,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140517905,"seq_region_name":"7","id":"rs1182352675","clinical_significance":[]},{"source":"dbSNP","start":140517907,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140517907,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1261368072"},{"clinical_significance":[],"seq_region_name":"7","id":"rs752064958","source":"dbSNP","start":140517908,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140517908,"alleles":["G","A"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140517910,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517910,"clinical_significance":[],"seq_region_name":"7","id":"rs780422207"},{"seq_region_name":"7","id":"rs1021959926","clinical_significance":[],"start":140517918,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140517918,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs996832787","clinical_significance":[],"end":140517919,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140517919,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1033260803","source":"dbSNP","start":140517920,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140517920,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1362879555","source":"dbSNP","start":140517925,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140517925,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1252364876","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517927,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140517927},{"clinical_significance":[],"seq_region_name":"7","id":"rs977950407","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517929,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140517929},{"seq_region_name":"7","id":"rs112126663","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517930,"source":"dbSNP","strand":1,"feature_type":"variation","end":140517930,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795721346","alleles":["A","C"],"end":140517932,"feature_type":"variation","strand":1,"source":"dbSNP","start":140517932,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1253961282","source":"dbSNP","start":140517935,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140517935,"alleles":["C","T"],"feature_type":"variation","strand":1},{"id":"rs1795721447","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","-"],"end":140517937,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517937,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140517938,"source":"dbSNP","strand":1,"feature_type":"variation","end":140517938,"alleles":["A","C"],"seq_region_name":"7","id":"rs1399003281","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1398488502","alleles":["G","T"],"end":140517939,"feature_type":"variation","strand":1,"source":"dbSNP","start":140517939,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1795721592","seq_region_name":"7","clinical_significance":[],"end":140517943,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140517943,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1277232873","clinical_significance":[],"start":140517945,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140517945,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1393998025","seq_region_name":"7","end":140517947,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140517947,"consequence_type":"splice_region_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130438183","consequence_type":"splice_donor_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517951,"feature_type":"variation","strand":1,"end":140517951,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1795721763","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"splice_region_variant","start":140517954,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CTCT","CT"],"end":140517957},{"clinical_significance":[],"seq_region_name":"7","id":"rs1031359981","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140517956,"consequence_type":"splice_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517956},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140517957,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517957,"clinical_significance":[],"seq_region_name":"7","id":"rs957295851"},{"start":140517957,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","alleles":["TTTTT","TTTT"],"end":140517961,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1563111141","clinical_significance":[]},{"alleles":["T","C"],"end":140517958,"feature_type":"variation","strand":1,"source":"dbSNP","start":140517958,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130438210"},{"start":140517958,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","alleles":["TTTTGT","T"],"end":140517963,"strand":1,"feature_type":"variation","id":"rs1563111148","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795722028","consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517960,"feature_type":"variation","strand":1,"end":140517960,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs145343703","feature_type":"variation","strand":1,"alleles":["TGTGTGTGTG","TGTGTGTGTGTG"],"end":140517970,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517961},{"clinical_significance":[],"id":"rs1563111158","seq_region_name":"7","end":140517963,"alleles":["-","AAAAAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140517964,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1421573429","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140517964,"source":"dbSNP","strand":1,"feature_type":"variation","end":140517964,"alleles":["G","A","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795722255","source":"dbSNP","start":140517967,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","end":140517967,"alleles":["T","C"],"feature_type":"variation","strand":1},{"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517968,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140517968,"clinical_significance":[],"seq_region_name":"7","id":"rs751891974"},{"seq_region_name":"7","id":"rs1795722354","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140517969,"source":"dbSNP","strand":1,"feature_type":"variation","end":140517969,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1795722408","clinical_significance":[],"end":140517970,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140517970,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant"},{"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517970,"feature_type":"variation","strand":1,"alleles":["GC","GCGC"],"end":140517971,"clinical_significance":[],"id":"rs1795722465","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140517974,"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140517974,"source":"dbSNP","id":"rs960643398","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517976,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140517976,"clinical_significance":[],"id":"rs1185908697","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140517980,"alleles":["G","A","C"],"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517980,"clinical_significance":[],"seq_region_name":"7","id":"rs1442154752"},{"id":"rs992050359","seq_region_name":"7","clinical_significance":[],"end":140517982,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140517982,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant"},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140517983,"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140517983,"source":"dbSNP","seq_region_name":"7","id":"rs1585532169","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140517985,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140517985,"source":"dbSNP","id":"rs1020017183","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140517986,"feature_type":"variation","strand":1,"end":140517986,"alleles":["G","T"],"clinical_significance":[],"id":"rs1201037566","seq_region_name":"7"},{"seq_region_name":"7","id":"rs971140067","clinical_significance":[],"start":140517987,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","end":140517987,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140517990,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","end":140517990,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795722846"},{"seq_region_name":"7","id":"rs1255588142","clinical_significance":[],"strand":1,"feature_type":"variation","end":140517996,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140517996,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795723024","clinical_significance":[],"start":140517997,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","alleles":["C","G","T"],"end":140517997,"strand":1,"feature_type":"variation"},{"alleles":["T","C"],"end":140518000,"strand":1,"feature_type":"variation","start":140518000,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","id":"rs1217422556","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140518003,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518003,"clinical_significance":[],"seq_region_name":"7","id":"rs1335074598"},{"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140518005,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140518005,"seq_region_name":"7","id":"rs1285547326","clinical_significance":[]},{"seq_region_name":"7","id":"rs1242408123","clinical_significance":[],"start":140518013,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","end":140518013,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140518015,"source":"dbSNP","strand":1,"feature_type":"variation","end":140518015,"alleles":["C","T"],"seq_region_name":"7","id":"rs1585532236","clinical_significance":[]},{"id":"rs1339626092","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140518015,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CTTCTTCT","CTTCT"],"end":140518022},{"end":140518016,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140518016,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs981129633","seq_region_name":"7"},{"alleles":["T","G"],"end":140518017,"strand":1,"feature_type":"variation","start":140518017,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","seq_region_name":"7","id":"rs1448891109","clinical_significance":[]},{"end":140518021,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140518021,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","seq_region_name":"7","id":"rs947998558","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140518022,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518022,"clinical_significance":[],"id":"rs142478270","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140518029,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140518029,"seq_region_name":"7","id":"rs1795723646","clinical_significance":[]},{"clinical_significance":[],"id":"rs1585532269","seq_region_name":"7","consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518030,"feature_type":"variation","strand":1,"end":140518030,"alleles":["C","A","G"]},{"end":140518033,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140518033,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1461994251","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1215602941","clinical_significance":[],"strand":1,"feature_type":"variation","end":140518034,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140518034,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140518036,"alleles":["A","C"],"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518036,"clinical_significance":[],"id":"rs1795723876","seq_region_name":"7"},{"start":140518037,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","end":140518037,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795723949","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795723999","source":"dbSNP","start":140518040,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","end":140518046,"alleles":["AAGAAGA","AAGA"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1161656048","feature_type":"variation","strand":1,"end":140518041,"alleles":["A","G","T"],"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518041},{"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140518042,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140518042,"seq_region_name":"7","id":"rs937151715","clinical_significance":[]},{"id":"rs1795724177","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140518044,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140518044},{"feature_type":"variation","strand":1,"alleles":["AGAG","AG"],"end":140518047,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518044,"clinical_significance":[],"id":"rs1364732004","seq_region_name":"7"},{"id":"rs1795724288","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140518044,"alleles":["-","TTCTT"],"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140518045,"source":"dbSNP"},{"alleles":["G","A","C"],"end":140518045,"feature_type":"variation","strand":1,"source":"dbSNP","start":140518045,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1181118681"},{"alleles":["G","C"],"end":140518047,"strand":1,"feature_type":"variation","start":140518047,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","seq_region_name":"7","id":"rs1795724407","clinical_significance":[]},{"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518049,"feature_type":"variation","strand":1,"end":140518049,"alleles":["C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795724468"},{"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518052,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140518052,"clinical_significance":[],"seq_region_name":"7","id":"rs974436859"},{"clinical_significance":[],"id":"rs1585532322","seq_region_name":"7","alleles":["T","G"],"end":140518053,"feature_type":"variation","strand":1,"source":"dbSNP","start":140518053,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1795724613","seq_region_name":"7","source":"dbSNP","start":140518054,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","end":140518054,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1238030600","seq_region_name":"7","alleles":["CA","-"],"end":140518056,"feature_type":"variation","strand":1,"source":"dbSNP","start":140518055,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140518056,"alleles":["A","T"],"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518056,"clinical_significance":[],"id":"rs1795724715","seq_region_name":"7"},{"source":"dbSNP","start":140518060,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","end":140518060,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs545771360"},{"source":"dbSNP","start":140518064,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","alleles":["AGAGAGA","AGAGA"],"end":140518070,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795724830","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140518067,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140518067,"seq_region_name":"7","id":"rs919846047","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140518069,"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140518069,"source":"dbSNP","id":"rs147561142","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518071,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140518071,"clinical_significance":[],"seq_region_name":"7","id":"rs1207697819"},{"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140518072,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140518072,"seq_region_name":"7","id":"rs113206406","clinical_significance":[]},{"clinical_significance":[],"id":"rs1291635378","seq_region_name":"7","alleles":["G","GG"],"end":140518072,"feature_type":"variation","strand":1,"source":"dbSNP","start":140518072,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38"},{"id":"rs1309732180","seq_region_name":"7","clinical_significance":[],"alleles":["T","A"],"end":140518073,"strand":1,"feature_type":"variation","start":140518073,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant"},{"strand":1,"feature_type":"variation","end":140518077,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140518077,"source":"dbSNP","id":"rs1047208436","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1374612606","clinical_significance":[],"start":140518079,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","end":140518079,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1795725363","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140518080,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140518080},{"clinical_significance":[],"seq_region_name":"7","id":"rs781462511","consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518083,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140518083},{"seq_region_name":"7","id":"rs543266102","clinical_significance":[],"start":140518084,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","alleles":["G","A"],"end":140518084,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140518085,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140518085,"seq_region_name":"7","id":"rs1795725538","clinical_significance":[]},{"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518096,"feature_type":"variation","strand":1,"end":140518096,"alleles":["G","A","C"],"clinical_significance":[],"id":"rs1351656246","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795725655","clinical_significance":[],"start":140518099,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","alleles":["T","C"],"end":140518099,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs944779067","clinical_significance":[],"end":140518104,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140518104,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1040418421","end":140518110,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140518110,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1039909458","source":"dbSNP","start":140518111,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","end":140518111,"alleles":["C","T"],"feature_type":"variation","strand":1},{"end":140518112,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140518112,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","seq_region_name":"7","id":"rs900704814","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795725868","consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518113,"feature_type":"variation","strand":1,"end":140518113,"alleles":["G","A"]},{"id":"rs995763381","seq_region_name":"7","clinical_significance":[],"end":140518120,"alleles":["C","-"],"strand":1,"feature_type":"variation","start":140518120,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant"},{"id":"rs1159807489","seq_region_name":"7","clinical_significance":[],"start":140518122,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","end":140518122,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"start":140518123,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","end":140518123,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs1795726032","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518124,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140518124,"clinical_significance":[],"seq_region_name":"7","id":"rs1247939155"},{"end":140518128,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140518128,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795726134"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140518130,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518130,"clinical_significance":[],"seq_region_name":"7","id":"rs996349199"},{"clinical_significance":[],"id":"rs1450691718","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140518134,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518134},{"source":"dbSNP","start":140518135,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","end":140518135,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795726229"},{"start":140518137,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","alleles":["C","A"],"end":140518137,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585532498","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140518143,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140518143,"seq_region_name":"7","id":"rs1795726341","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs140324153","consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518144,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140518144},{"seq_region_name":"7","id":"rs770851365","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140518149,"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140518149,"source":"dbSNP"},{"alleles":["G","A","T"],"end":140518151,"strand":1,"feature_type":"variation","start":140518151,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","seq_region_name":"7","id":"rs1351207096","clinical_significance":[]},{"end":140518156,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140518156,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1285270451","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs368083698","end":140518157,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140518157,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38"},{"id":"rs529407583","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140518158,"source":"dbSNP","strand":1,"feature_type":"variation","end":140518158,"alleles":["T","C"]},{"clinical_significance":[],"id":"rs1585532561","seq_region_name":"7","consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518159,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140518159},{"clinical_significance":[],"id":"rs73492323","seq_region_name":"7","source":"dbSNP","start":140518160,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140518160,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1585532589","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140518162,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140518162},{"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140518164,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140518164,"seq_region_name":"7","id":"rs1438189344","clinical_significance":[]},{"alleles":["T","C"],"end":140518166,"feature_type":"variation","strand":1,"source":"dbSNP","start":140518166,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs2130438660","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1291362402","clinical_significance":[],"strand":1,"feature_type":"variation","end":140518167,"alleles":["A","AA"],"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140518167,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795726983","feature_type":"variation","strand":1,"end":140518167,"alleles":["A","T"],"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518167},{"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518168,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140518168,"clinical_significance":[],"seq_region_name":"7","id":"rs1795727095"},{"id":"rs1327276102","seq_region_name":"7","clinical_significance":[],"start":140518169,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","end":140518169,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs566168935","source":"dbSNP","start":140518174,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","end":140518174,"alleles":["A","G"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140518175,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140518175,"seq_region_name":"7","id":"rs1795727254","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140518177,"source":"dbSNP","strand":1,"feature_type":"variation","end":140518177,"alleles":["C","T"],"seq_region_name":"7","id":"rs1585532636","clinical_significance":[]},{"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518178,"feature_type":"variation","strand":1,"end":140518178,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795727354"},{"end":140518183,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140518183,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","seq_region_name":"7","id":"rs1795727408","clinical_significance":[]},{"alleles":["G","C"],"end":140518186,"feature_type":"variation","strand":1,"source":"dbSNP","start":140518186,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795727467"},{"alleles":["G","A"],"end":140518188,"strand":1,"feature_type":"variation","start":140518188,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","seq_region_name":"7","id":"rs1795727507","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1398589455","end":140518191,"alleles":["CCC","CCCCC"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140518189,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140518191,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140518191,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795727627"},{"clinical_significance":[],"id":"rs1795727686","seq_region_name":"7","consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518193,"feature_type":"variation","strand":1,"end":140518193,"alleles":["G","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs971003831","consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518200,"feature_type":"variation","strand":1,"end":140518200,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs1795727785","clinical_significance":[],"start":140518201,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","end":140518201,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140518202,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","end":140518202,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795727837"},{"seq_region_name":"7","id":"rs74327254","clinical_significance":[],"strand":1,"feature_type":"variation","end":140518207,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140518207,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140518208,"source":"dbSNP","strand":1,"feature_type":"variation","end":140518208,"alleles":["G","A"],"id":"rs1174887424","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795728016","clinical_significance":[],"alleles":["C","T"],"end":140518210,"strand":1,"feature_type":"variation","start":140518210,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795728071","feature_type":"variation","strand":1,"end":140518212,"alleles":["C","T"],"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518212},{"seq_region_name":"7","id":"rs1034100587","clinical_significance":[],"start":140518213,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","end":140518213,"alleles":["A","C","G","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs190817644","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140518214,"source":"dbSNP","strand":1,"feature_type":"variation","end":140518214,"alleles":["C","A","G"]},{"start":140518219,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","end":140518219,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs1795728240","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140518222,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140518222,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1585532696","seq_region_name":"7"},{"start":140518223,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","end":140518223,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1240185273","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795728382","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140518224,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140518224},{"clinical_significance":[],"seq_region_name":"7","id":"rs370104743","source":"dbSNP","start":140518225,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","end":140518225,"alleles":["C","T"],"feature_type":"variation","strand":1},{"id":"rs1170330865","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140518226,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140518226,"source":"dbSNP"},{"id":"rs1477381579","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140518229,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140518229},{"alleles":["C","A"],"end":140518232,"feature_type":"variation","strand":1,"source":"dbSNP","start":140518232,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1311438301"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1195354765","consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518233,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140518233},{"seq_region_name":"7","id":"rs1795728881","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140518234,"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140518234,"source":"dbSNP"},{"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518235,"feature_type":"variation","strand":1,"end":140518235,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795728954"},{"clinical_significance":[],"id":"rs1351380784","seq_region_name":"7","consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518238,"feature_type":"variation","strand":1,"end":140518238,"alleles":["C","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs114542045","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140518239,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518239},{"seq_region_name":"7","id":"rs973914591","clinical_significance":[],"start":140518240,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","end":140518240,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140518242,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140518242,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1453044153","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1013513202","feature_type":"variation","strand":1,"end":140518244,"alleles":["C","T"],"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518244},{"id":"rs1795729456","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140518245,"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140518245,"source":"dbSNP"},{"start":140518246,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","end":140518246,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795729510","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795729563","clinical_significance":[],"end":140518247,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140518247,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant"},{"id":"rs1795729620","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140518250,"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140518250,"source":"dbSNP"},{"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518253,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140518253,"clinical_significance":[],"seq_region_name":"7","id":"rs919730642"},{"end":140518254,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140518254,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","seq_region_name":"7","id":"rs144287682","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1218741568","feature_type":"variation","strand":1,"end":140518255,"alleles":["A","C"],"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518255},{"end":140518256,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140518256,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs969413040"},{"source":"dbSNP","start":140518259,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140518259,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs745608618","seq_region_name":"7"},{"seq_region_name":"7","id":"rs982660359","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140518261,"source":"dbSNP","strand":1,"feature_type":"variation","end":140518261,"alleles":["C","T"]},{"alleles":["A","G"],"end":140518262,"strand":1,"feature_type":"variation","start":140518262,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","id":"rs2130438893","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","C"],"end":140518263,"strand":1,"feature_type":"variation","start":140518263,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","id":"rs1795730020","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1398371407","clinical_significance":[],"alleles":["C","A","T"],"end":140518268,"strand":1,"feature_type":"variation","start":140518268,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant"},{"alleles":["G","A","C"],"end":140518269,"feature_type":"variation","strand":1,"source":"dbSNP","start":140518269,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs374389269"},{"id":"rs1450585419","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140518273,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140518273,"source":"dbSNP"},{"seq_region_name":"7","id":"rs771827700","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140518277,"source":"dbSNP","strand":1,"feature_type":"variation","end":140518277,"alleles":["C","T"]},{"alleles":["G","A","T"],"end":140518278,"strand":1,"feature_type":"variation","start":140518278,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","seq_region_name":"7","id":"rs1179299120","clinical_significance":[]},{"seq_region_name":"7","id":"rs907876891","clinical_significance":[],"alleles":["C","T"],"end":140518282,"strand":1,"feature_type":"variation","start":140518282,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs537710726","alleles":["G","A"],"end":140518283,"feature_type":"variation","strand":1,"source":"dbSNP","start":140518283,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38"},{"end":140518286,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140518286,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","seq_region_name":"7","id":"rs555545222","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","C","T"],"end":140518288,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518288,"clinical_significance":[],"seq_region_name":"7","id":"rs1438369937"},{"id":"rs1795730545","seq_region_name":"7","clinical_significance":[],"alleles":["C","G"],"end":140518289,"strand":1,"feature_type":"variation","start":140518289,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant"},{"seq_region_name":"7","id":"rs1795730594","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140518291,"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140518291,"source":"dbSNP"},{"end":140518294,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140518294,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795730651"},{"end":140518295,"alleles":["A","C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140518295,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1158513628"},{"seq_region_name":"7","id":"rs1795730777","clinical_significance":[],"end":140518301,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140518301,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795730833","consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518304,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140518304},{"seq_region_name":"7","id":"rs1422385551","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140518311,"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140518311,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs775107350","feature_type":"variation","strand":1,"end":140518312,"alleles":["C","G","T"],"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518312},{"start":140518313,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","end":140518313,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795731021","clinical_significance":[]},{"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518315,"feature_type":"variation","strand":1,"end":140518315,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1414982433"},{"seq_region_name":"7","id":"rs1795731136","clinical_significance":[],"alleles":["CTCCTC","CTC"],"end":140518320,"strand":1,"feature_type":"variation","start":140518315,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant"},{"id":"rs1484081319","seq_region_name":"7","clinical_significance":[],"alleles":["C","G","T"],"end":140518317,"strand":1,"feature_type":"variation","start":140518317,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant"},{"source":"dbSNP","start":140518318,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140518318,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1040891492"},{"seq_region_name":"7","id":"rs1795731254","clinical_significance":[],"start":140518319,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","end":140518319,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518320,"feature_type":"variation","strand":1,"end":140518320,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1209294559"},{"alleles":["T","C"],"end":140518322,"feature_type":"variation","strand":1,"source":"dbSNP","start":140518322,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130439021"},{"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518323,"feature_type":"variation","strand":1,"end":140518323,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795731363"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140518324,"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140518324,"source":"dbSNP","seq_region_name":"7","id":"rs1458321385","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140518326,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140518326,"id":"rs180823346","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795731502","feature_type":"variation","strand":1,"end":140518327,"alleles":["C","T"],"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518327},{"id":"rs932167815","seq_region_name":"7","clinical_significance":[],"start":140518328,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","alleles":["C","T"],"end":140518328,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1317552695","clinical_significance":[],"end":140518329,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140518329,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant"},{"feature_type":"variation","strand":1,"end":140518330,"alleles":["T","C"],"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518330,"clinical_significance":[],"seq_region_name":"7","id":"rs983241315"},{"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518331,"feature_type":"variation","strand":1,"end":140518331,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1313646671"},{"alleles":["T","C"],"end":140518334,"strand":1,"feature_type":"variation","start":140518334,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","seq_region_name":"7","id":"rs1795731778","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140518338,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518338,"clinical_significance":[],"seq_region_name":"7","id":"rs1162290737"},{"clinical_significance":[],"seq_region_name":"7","id":"rs750105323","consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518339,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140518339},{"clinical_significance":[],"id":"rs1795731964","seq_region_name":"7","consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518340,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140518340},{"alleles":["C","A"],"end":140518341,"strand":1,"feature_type":"variation","start":140518341,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","seq_region_name":"7","id":"rs199828930","clinical_significance":[]},{"alleles":["C","T"],"end":140518342,"feature_type":"variation","strand":1,"source":"dbSNP","start":140518342,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs186219631","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs760367355","consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518343,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140518343},{"seq_region_name":"7","id":"rs1332796488","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140518344,"source":"dbSNP","strand":1,"feature_type":"variation","end":140518344,"alleles":["G","A"]},{"alleles":["G","A"],"end":140518349,"strand":1,"feature_type":"variation","start":140518349,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","seq_region_name":"7","id":"rs1463566583","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs572087450","feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140518351,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518351},{"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140518352,"source":"dbSNP","strand":1,"feature_type":"variation","end":140518352,"alleles":["G","A"],"seq_region_name":"7","id":"rs1425373032","clinical_significance":[]},{"source":"dbSNP","start":140518353,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140518353,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1411344949"},{"end":140518355,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140518355,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1020455214","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1239895379","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140518356,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140518356},{"id":"rs1795732566","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140518358,"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140518358,"source":"dbSNP"},{"source":"dbSNP","start":140518361,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140518361,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795732651"},{"clinical_significance":[],"seq_region_name":"7","id":"rs944171032","feature_type":"variation","strand":1,"end":140518364,"alleles":["C","T"],"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518364},{"seq_region_name":"7","id":"rs1284664206","clinical_significance":[],"alleles":["G","A","T"],"end":140518365,"strand":1,"feature_type":"variation","start":140518365,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant"},{"source":"dbSNP","start":140518367,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","end":140518367,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1266304847","seq_region_name":"7"},{"seq_region_name":"7","id":"rs906918233","clinical_significance":[],"alleles":["G","A"],"end":140518375,"strand":1,"feature_type":"variation","start":140518375,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant"},{"seq_region_name":"7","id":"rs533635222","clinical_significance":[],"start":140518378,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","end":140518378,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1226375943","clinical_significance":[],"start":140518380,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","alleles":["G","A"],"end":140518380,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795733154","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140518381,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518381},{"clinical_significance":[],"id":"rs921507772","seq_region_name":"7","source":"dbSNP","start":140518385,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140518385,"feature_type":"variation","strand":1},{"alleles":["T","C"],"end":140518388,"feature_type":"variation","strand":1,"source":"dbSNP","start":140518388,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1288038783"},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140518397,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518397,"clinical_significance":[],"id":"rs1585533192","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140518399,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518399,"clinical_significance":[],"id":"rs1795733380","seq_region_name":"7"},{"seq_region_name":"7","id":"rs2130439201","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140518403,"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140518403,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1241244297","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140518404,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140518404},{"clinical_significance":[],"seq_region_name":"7","id":"rs1034543088","end":140518407,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140518407,"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1334435153","clinical_significance":[],"alleles":["A","-"],"end":140518408,"strand":1,"feature_type":"variation","start":140518408,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant"},{"feature_type":"variation","strand":1,"end":140518409,"alleles":["G","T"],"consequence_type":"regulatory_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518409,"clinical_significance":[],"seq_region_name":"7","id":"rs1199415979"},{"id":"rs1443995063","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","start":140518415,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140518415},{"start":140518417,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"regulatory_region_variant","end":140518417,"alleles":["A","G"],"strand":1,"feature_type":"variation","id":"rs1371941022","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140518418,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140518418,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795733770"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140518420,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140518420,"source":"dbSNP","seq_region_name":"7","id":"rs1795733827","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795733908","feature_type":"variation","strand":1,"end":140518421,"alleles":["A","G"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518421},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140518422,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518422,"clinical_significance":[],"id":"rs1795733982","seq_region_name":"7"},{"seq_region_name":"7","id":"rs931674520","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140518435,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140518435},{"clinical_significance":[],"seq_region_name":"7","id":"rs1459136368","source":"dbSNP","start":140518438,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140518438,"alleles":["T","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795734143","clinical_significance":[],"alleles":["T","C"],"end":140518440,"strand":1,"feature_type":"variation","start":140518440,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"alleles":["T","A"],"end":140518442,"feature_type":"variation","strand":1,"source":"dbSNP","start":140518442,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1394694918"},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518443,"feature_type":"variation","strand":1,"end":140518443,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795734299"},{"seq_region_name":"7","id":"rs1795734383","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140518445,"source":"dbSNP","strand":1,"feature_type":"variation","end":140518445,"alleles":["G","C"]},{"strand":1,"feature_type":"variation","end":140518447,"alleles":["T","TT"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140518447,"source":"dbSNP","seq_region_name":"7","id":"rs1795734479","clinical_significance":[]},{"id":"rs768118597","seq_region_name":"7","clinical_significance":[],"alleles":["A","T"],"end":140518448,"strand":1,"feature_type":"variation","start":140518448,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"id":"rs58426584","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140518458,"alleles":["AAAAAAAAAAA","AAAAAAA","AAAAAAAAA","AAAAAAAAAA","AAAAAAAAAAAA"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140518448,"source":"dbSNP"},{"id":"rs1795734860","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140518449,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140518449},{"alleles":["A","T"],"end":140518455,"strand":1,"feature_type":"variation","start":140518455,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","id":"rs1181759064","seq_region_name":"7","clinical_significance":[]},{"end":140518458,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140518458,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs545506102","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1238510860","clinical_significance":[],"start":140518459,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["C","A"],"end":140518459,"strand":1,"feature_type":"variation"},{"id":"rs62485801","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140518461,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140518461,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140518463,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518463,"clinical_significance":[],"seq_region_name":"7","id":"rs1795735491"},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518468,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140518468,"clinical_significance":[],"seq_region_name":"7","id":"rs999303363"},{"source":"dbSNP","start":140518469,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140518469,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1192933004"},{"clinical_significance":[],"id":"rs1795735918","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","T"],"end":140518475,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518475},{"start":140518476,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140518476,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs958499082","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140518476,"source":"dbSNP","strand":1,"feature_type":"variation","end":140518478,"alleles":["CCC","CC"],"id":"rs1474009353","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","G"],"end":140518479,"strand":1,"feature_type":"variation","start":140518479,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs1585533360","clinical_significance":[]},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518480,"feature_type":"variation","strand":1,"end":140518480,"alleles":["T","C"],"clinical_significance":[],"id":"rs1795736487","seq_region_name":"7"},{"clinical_significance":[],"id":"rs995635229","seq_region_name":"7","feature_type":"variation","strand":1,"end":140518484,"alleles":["C","T"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518484},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518485,"feature_type":"variation","strand":1,"end":140518485,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795736771"},{"feature_type":"variation","strand":1,"end":140518487,"alleles":["G","T"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518487,"clinical_significance":[],"seq_region_name":"7","id":"rs1795736898"},{"source":"dbSNP","start":140518489,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140518489,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1026826471","seq_region_name":"7"},{"source":"dbSNP","start":140518490,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140518490,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1240049007"},{"source":"dbSNP","start":140518492,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140518492,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs951152610"},{"id":"rs1412711667","seq_region_name":"7","clinical_significance":[],"end":140518493,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140518493,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"seq_region_name":"7","id":"rs1795737605","clinical_significance":[],"alleles":["C","T"],"end":140518495,"strand":1,"feature_type":"variation","start":140518495,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"id":"rs191081679","seq_region_name":"7","clinical_significance":[],"start":140518497,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140518497,"alleles":["C","G","T"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140518498,"alleles":["G","A"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518498,"clinical_significance":[],"seq_region_name":"7","id":"rs912473341"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140518507,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518507,"clinical_significance":[],"seq_region_name":"7","id":"rs1302121017"},{"alleles":["G","A","C"],"end":140518508,"feature_type":"variation","strand":1,"source":"dbSNP","start":140518508,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs377454904","seq_region_name":"7"},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518509,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140518509,"clinical_significance":[],"seq_region_name":"7","id":"rs1795738379"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795738459","source":"dbSNP","start":140518512,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140518512,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795738537","clinical_significance":[],"strand":1,"feature_type":"variation","end":140518517,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140518517,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1052577247","feature_type":"variation","strand":1,"end":140518520,"alleles":["T","C","G"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518520},{"clinical_significance":[],"seq_region_name":"7","id":"rs896329707","end":140518523,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140518523,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"alleles":["G","C"],"end":140518527,"strand":1,"feature_type":"variation","start":140518527,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs543652695","clinical_significance":[]},{"end":140518529,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140518529,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1178361287"},{"seq_region_name":"7","id":"rs114080575","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140518532,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140518532},{"end":140518533,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140518533,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585533458"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1268503577","source":"dbSNP","start":140518534,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140518534,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1023594613","clinical_significance":[],"alleles":["C","A","T"],"end":140518538,"strand":1,"feature_type":"variation","start":140518538,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518539,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140518539,"clinical_significance":[],"seq_region_name":"7","id":"rs573921957"},{"clinical_significance":[],"id":"rs1795739393","seq_region_name":"7","alleles":["G","A"],"end":140518540,"feature_type":"variation","strand":1,"source":"dbSNP","start":140518540,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140518545,"source":"dbSNP","strand":1,"feature_type":"variation","end":140518545,"alleles":["C","A"],"id":"rs2130439669","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795739483","source":"dbSNP","start":140518547,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140518547,"alleles":["G","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs932100639","seq_region_name":"7","source":"dbSNP","start":140518548,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140518548,"feature_type":"variation","strand":1},{"alleles":["C","T"],"end":140518551,"strand":1,"feature_type":"variation","start":140518551,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","id":"rs1216263578","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1346369272","source":"dbSNP","start":140518553,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140518553,"feature_type":"variation","strand":1},{"alleles":["T","C"],"end":140518555,"strand":1,"feature_type":"variation","start":140518555,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","id":"rs1795739880","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795739951","clinical_significance":[],"start":140518557,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140518557,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1795740015","clinical_significance":[],"alleles":["A","G"],"end":140518558,"strand":1,"feature_type":"variation","start":140518558,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"seq_region_name":"7","id":"rs1795740109","clinical_significance":[],"strand":1,"feature_type":"variation","end":140518561,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140518561,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130439728","end":140518562,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140518562,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1054915677","clinical_significance":[],"end":140518570,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140518570,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"seq_region_name":"7","id":"rs1795740304","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140518574,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140518574},{"seq_region_name":"7","id":"rs914746152","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140518575,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140518575},{"seq_region_name":"7","id":"rs780053859","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140518576,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140518576},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518581,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140518581,"clinical_significance":[],"seq_region_name":"7","id":"rs147788008"},{"seq_region_name":"7","id":"rs1795740727","clinical_significance":[],"start":140518585,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140518585,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518587,"feature_type":"variation","strand":1,"end":140518587,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795740834"},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518588,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140518588,"clinical_significance":[],"seq_region_name":"7","id":"rs1218849657"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140518589,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518589,"clinical_significance":[],"seq_region_name":"7","id":"rs181086892"},{"clinical_significance":[],"seq_region_name":"7","id":"rs533437224","alleles":["G","A"],"end":140518590,"feature_type":"variation","strand":1,"source":"dbSNP","start":140518590,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs879791830","alleles":["C","T"],"end":140518591,"feature_type":"variation","strand":1,"source":"dbSNP","start":140518591,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"start":140518592,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140518592,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs894098574","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1304487670","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140518594,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518594},{"alleles":["C","A"],"end":140518603,"feature_type":"variation","strand":1,"source":"dbSNP","start":140518603,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1195285280"},{"feature_type":"variation","strand":1,"end":140518604,"alleles":["C","T"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518604,"clinical_significance":[],"seq_region_name":"7","id":"rs185526072"},{"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140518605,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140518605,"source":"dbSNP","seq_region_name":"7","id":"rs376350934","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140518606,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140518606,"source":"dbSNP","seq_region_name":"7","id":"rs1795741701","clinical_significance":[]},{"source":"dbSNP","start":140518607,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140518607,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs951226124"},{"seq_region_name":"7","id":"rs1795741866","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140518608,"source":"dbSNP","strand":1,"feature_type":"variation","end":140518608,"alleles":["C","A"]},{"source":"dbSNP","start":140518609,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140518609,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs530807865"},{"id":"rs549307990","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140518610,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140518610,"source":"dbSNP"},{"clinical_significance":[],"id":"rs567606829","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140518611,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518611},{"seq_region_name":"7","id":"rs1192951999","clinical_significance":[],"start":140518611,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140518611,"alleles":["T","TT"],"strand":1,"feature_type":"variation"},{"start":140518612,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140518612,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795742321","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs369605774","feature_type":"variation","strand":1,"alleles":["A","T"],"end":140518615,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518615},{"alleles":["A","C"],"end":140518616,"strand":1,"feature_type":"variation","start":140518616,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","id":"rs1258926427","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs975535126","source":"dbSNP","start":140518617,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140518617,"alleles":["C","G","T"],"feature_type":"variation","strand":1},{"alleles":["T","C"],"end":140518619,"strand":1,"feature_type":"variation","start":140518619,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","id":"rs2130439982","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518620,"feature_type":"variation","strand":1,"end":140518620,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs921548173"},{"seq_region_name":"7","id":"rs1198652426","clinical_significance":[],"end":140518621,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140518621,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518622,"feature_type":"variation","strand":1,"end":140518622,"alleles":["G","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs947654075"},{"source":"dbSNP","start":140518628,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140518628,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs979400787"},{"feature_type":"variation","strand":1,"end":140518629,"alleles":["C","T"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518629,"clinical_significance":[],"seq_region_name":"7","id":"rs1795743009"},{"id":"rs924978017","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140518633,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140518633,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1195421747","seq_region_name":"7","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518635,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140518635},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518639,"feature_type":"variation","strand":1,"end":140518639,"alleles":["A","G"],"clinical_significance":[],"id":"rs965343994","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795743365","clinical_significance":[],"alleles":["G","A"],"end":140518640,"strand":1,"feature_type":"variation","start":140518640,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"end":140518641,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140518641,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs550708833","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140518643,"source":"dbSNP","strand":1,"feature_type":"variation","end":140518643,"alleles":["C","T"],"seq_region_name":"7","id":"rs1420989290","clinical_significance":[]},{"end":140518644,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","start":140518644,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","id":"rs1795743637","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518645,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140518645,"clinical_significance":[],"seq_region_name":"7","id":"rs934959473"},{"clinical_significance":[],"seq_region_name":"7","id":"rs975709670","end":140518646,"alleles":["C","A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140518646,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs73735368","clinical_significance":[],"alleles":["A","C"],"end":140518647,"strand":1,"feature_type":"variation","start":140518647,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"start":140518648,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140518648,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1405187731","clinical_significance":[]},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518649,"feature_type":"variation","strand":1,"end":140518649,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795744127"},{"seq_region_name":"7","id":"rs1052227659","clinical_significance":[],"strand":1,"feature_type":"variation","end":140518653,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140518653,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795744308","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140518654,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518654},{"feature_type":"variation","strand":1,"end":140518656,"alleles":["T","C"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518656,"clinical_significance":[],"seq_region_name":"7","id":"rs921964356"},{"seq_region_name":"7","id":"rs6852","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140518664,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","G","T"],"end":140518664},{"clinical_significance":[],"seq_region_name":"7","id":"rs1459055500","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518666,"feature_type":"variation","strand":1,"end":140518666,"alleles":["T","C"]},{"end":140518667,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140518667,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1179705854","seq_region_name":"7"},{"id":"rs774352280","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140518668,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140518668,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1044905841","seq_region_name":"7","source":"dbSNP","start":140518669,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140518669,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs2130440192","clinical_significance":[],"strand":1,"feature_type":"variation","end":140518673,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140518673,"source":"dbSNP"},{"id":"rs1795745074","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140518675,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140518675,"source":"dbSNP"},{"alleles":["C","A","T"],"end":140518676,"feature_type":"variation","strand":1,"source":"dbSNP","start":140518676,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs761711360"},{"seq_region_name":"7","id":"rs773176958","clinical_significance":[],"start":140518679,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["G","C"],"end":140518679,"strand":1,"feature_type":"variation"},{"alleles":["GGAGG","G"],"end":140518683,"feature_type":"variation","strand":1,"source":"dbSNP","start":140518679,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795745345"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140518680,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518680,"clinical_significance":[],"seq_region_name":"7","id":"rs760360375"},{"source":"dbSNP","start":140518682,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140518682,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1171857356"},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518683,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140518683,"clinical_significance":[],"id":"rs766151130","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1408753319","alleles":["G","A"],"end":140518686,"feature_type":"variation","strand":1,"source":"dbSNP","start":140518686,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518687,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140518687,"clinical_significance":[],"seq_region_name":"7","id":"rs1326256362"},{"start":140518688,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140518688,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs753340856","clinical_significance":[]},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518689,"feature_type":"variation","strand":1,"end":140518689,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795745942"},{"source":"dbSNP","start":140518691,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140518693,"alleles":["CCC","CCCC"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs35549110"},{"id":"rs990290557","seq_region_name":"7","clinical_significance":[],"start":140518696,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140518696,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1795746157","clinical_significance":[],"strand":1,"feature_type":"variation","end":140518699,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140518699,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1351579701","clinical_significance":[],"alleles":["C","G"],"end":140518700,"strand":1,"feature_type":"variation","start":140518700,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795746336","feature_type":"variation","strand":1,"end":140518702,"alleles":["G","C"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518702},{"seq_region_name":"7","id":"rs1473369415","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["GAGAG","G","GAG"],"end":140518706,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140518702,"source":"dbSNP"},{"alleles":["A","G"],"end":140518705,"feature_type":"variation","strand":1,"source":"dbSNP","start":140518705,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs759120157"},{"clinical_significance":[],"seq_region_name":"7","id":"rs764720501","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518706,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140518706},{"source":"dbSNP","start":140518707,"consequence_type":"stop_retained_variant","assembly_name":"GRCh38","end":140518707,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1353197709"},{"source":"dbSNP","start":140518708,"consequence_type":"stop_lost","assembly_name":"GRCh38","alleles":["T","A"],"end":140518708,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1232406686"},{"seq_region_name":"7","id":"rs1795746824","clinical_significance":[],"strand":1,"feature_type":"variation","end":140518710,"alleles":["T","C","G"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140518710,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1437020313","source":"dbSNP","start":140518718,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140518718,"feature_type":"variation","strand":1},{"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518719,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140518719,"clinical_significance":[],"id":"rs1795747054","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140518721,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140518721,"seq_region_name":"7","id":"rs1563112044","clinical_significance":[]},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518723,"feature_type":"variation","strand":1,"end":140518723,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795747229"},{"clinical_significance":[],"seq_region_name":"7","id":"rs753236055","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140518731,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518731},{"seq_region_name":"7","id":"rs995453114","clinical_significance":[],"start":140518734,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["A","C"],"end":140518734,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs755010227","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518735,"feature_type":"variation","strand":1,"end":140518735,"alleles":["T","G"]},{"id":"rs1341357797","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"splice_region_variant","start":140518741,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140518741},{"id":"rs771987437","seq_region_name":"7","clinical_significance":[],"alleles":["AAAAAAAA","AAAAAAA","AAAAAAAAA"],"end":140518748,"strand":1,"feature_type":"variation","start":140518741,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_polypyrimidine_tract_variant"},{"seq_region_name":"7","id":"rs1795747878","clinical_significance":[],"end":140518745,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140518745,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_region_variant"},{"id":"rs758880834","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"splice_polypyrimidine_tract_variant","start":140518747,"source":"dbSNP","strand":1,"feature_type":"variation","end":140518747,"alleles":["A","G"]},{"clinical_significance":[],"id":"rs565655946","seq_region_name":"7","feature_type":"variation","strand":1,"end":140518748,"alleles":["A","G"],"consequence_type":"splice_polypyrimidine_tract_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518748},{"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140518749,"assembly_name":"GRCh38","consequence_type":"splice_polypyrimidine_tract_variant","start":140518749,"source":"dbSNP","seq_region_name":"7","id":"rs1795748170","clinical_significance":[]},{"seq_region_name":"7","id":"rs1458697967","clinical_significance":[],"start":140518750,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_polypyrimidine_tract_variant","end":140518750,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1795748372","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"splice_polypyrimidine_tract_variant","start":140518751,"source":"dbSNP","strand":1,"feature_type":"variation","end":140518751,"alleles":["A","G"]},{"source":"dbSNP","start":140518752,"consequence_type":"splice_polypyrimidine_tract_variant","assembly_name":"GRCh38","end":140518752,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795748467","seq_region_name":"7"},{"source":"dbSNP","start":140518756,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140518756,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1194867149"},{"id":"rs746778251","seq_region_name":"7","clinical_significance":[],"start":140518756,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140518758,"alleles":["GAG","-"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1212352745","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518757,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140518757},{"start":140518763,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140518763,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs751952552","seq_region_name":"7","clinical_significance":[]},{"start":140518766,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140518766,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs1563112077","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140518767,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140518767,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs757426098"},{"seq_region_name":"7","id":"rs750963515","clinical_significance":[],"end":140518768,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140518768,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140518769,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140518769,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs745883825"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518773,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140518773,"clinical_significance":[],"seq_region_name":"7","id":"rs756218016"},{"seq_region_name":"7","id":"rs73492325","clinical_significance":[],"start":140518781,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140518781,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140518784,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518784,"clinical_significance":[],"id":"rs748083878","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140518786,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140518786,"source":"dbSNP","seq_region_name":"7","id":"rs1278402451","clinical_significance":[]},{"seq_region_name":"7","id":"rs771930149","clinical_significance":[],"start":140518787,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140518787,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140518788,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518788,"clinical_significance":[],"seq_region_name":"7","id":"rs1795749847"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1314204374","source":"dbSNP","start":140518789,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140518789,"alleles":["A","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1373202526","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518790,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140518790},{"seq_region_name":"7","id":"rs879664409","clinical_significance":[],"alleles":["T","C"],"end":140518792,"strand":1,"feature_type":"variation","start":140518792,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1226877918","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518800,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140518800},{"clinical_significance":[],"id":"rs1795750294","seq_region_name":"7","source":"dbSNP","start":140518804,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140518804,"feature_type":"variation","strand":1},{"end":140518813,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140518813,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs928777689","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1381976171","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140518817,"source":"dbSNP","strand":1,"feature_type":"variation","end":140518817,"alleles":["G","A","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130440703","end":140518819,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140518819,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1004612458","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140518820,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518820},{"seq_region_name":"7","id":"rs938954431","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140518822,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140518822},{"alleles":["C","T"],"end":140518823,"strand":1,"feature_type":"variation","start":140518823,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1056410482","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140518824,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518824,"clinical_significance":[],"seq_region_name":"7","id":"rs765303644"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563112162","source":"dbSNP","start":140518825,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140518825,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1347128938","source":"dbSNP","start":140518827,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","TT"],"end":140518827,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518830,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140518830,"clinical_significance":[],"seq_region_name":"7","id":"rs544528170"},{"clinical_significance":[],"seq_region_name":"7","id":"rs117680338","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518831,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140518831},{"alleles":["G","A","C"],"end":140518832,"strand":1,"feature_type":"variation","start":140518832,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795751422","clinical_significance":[]},{"source":"dbSNP","start":140518834,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140518834,"alleles":["G","A","C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs886837301"},{"seq_region_name":"7","id":"rs1795751682","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140518835,"source":"dbSNP","strand":1,"feature_type":"variation","end":140518835,"alleles":["C","T"]},{"source":"dbSNP","start":140518837,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140518837,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1393066729"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1488847955","source":"dbSNP","start":140518839,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140518839,"feature_type":"variation","strand":1},{"end":140518840,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140518840,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1028467151"},{"clinical_significance":[],"seq_region_name":"7","id":"rs537032680","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518841,"feature_type":"variation","strand":1,"alleles":["C","A","G","T"],"end":140518841},{"clinical_significance":[],"seq_region_name":"7","id":"rs1019474599","source":"dbSNP","start":140518842,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140518842,"alleles":["G","A"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140518845,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140518845,"id":"rs1585534236","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","T"],"end":140518847,"strand":1,"feature_type":"variation","start":140518847,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs140221572","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140518850,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","AA"],"end":140518850,"seq_region_name":"7","id":"rs1795752518","clinical_significance":[]},{"end":140518850,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140518850,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130440890"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795752620","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518852,"feature_type":"variation","strand":1,"end":140518852,"alleles":["G","A"]},{"clinical_significance":[],"id":"rs376358650","seq_region_name":"7","end":140518855,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140518855,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140518860,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140518860,"seq_region_name":"7","id":"rs1795752832","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795752935","clinical_significance":[],"end":140518863,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140518863,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795753027","clinical_significance":[],"start":140518872,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140518872,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1795753116","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140518874,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140518874,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140518877,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518877,"clinical_significance":[],"seq_region_name":"7","id":"rs1441070287"},{"strand":1,"feature_type":"variation","end":140518878,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140518878,"source":"dbSNP","seq_region_name":"7","id":"rs1585534279","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1230661901","feature_type":"variation","strand":1,"alleles":["CC","C"],"end":140518880,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518879},{"alleles":["A","G"],"end":140518882,"feature_type":"variation","strand":1,"source":"dbSNP","start":140518882,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs573960665"},{"seq_region_name":"7","id":"rs935052867","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140518884,"source":"dbSNP","strand":1,"feature_type":"variation","end":140518884,"alleles":["G","A","C"]},{"end":140518885,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140518885,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs751800699"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518887,"feature_type":"variation","strand":1,"alleles":["G","C","T"],"end":140518887,"clinical_significance":[],"seq_region_name":"7","id":"rs1358429825"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795753988","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518888,"feature_type":"variation","strand":1,"end":140518888,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1795754091","clinical_significance":[],"end":140518892,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140518892,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1286734102","end":140518903,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140518903,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140518906,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","start":140518906,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1242216144","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1476733922","source":"dbSNP","start":140518909,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140518909,"alleles":["C","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs996780111","clinical_significance":[],"alleles":["C","T"],"end":140518910,"strand":1,"feature_type":"variation","start":140518910,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140518911,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140518911,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1380817562"},{"id":"rs1437230690","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140518912,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140518912},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795754748","source":"dbSNP","start":140518915,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140518915,"alleles":["G","A"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518918,"feature_type":"variation","strand":1,"end":140518918,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1421334230"},{"source":"dbSNP","start":140518925,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140518925,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1321800647"},{"clinical_significance":[],"id":"rs1585534404","seq_region_name":"7","end":140518927,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140518927,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140518929,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140518929,"source":"dbSNP","seq_region_name":"7","id":"rs75842547","clinical_significance":[]},{"source":"dbSNP","start":140518930,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140518930,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs953440398"},{"seq_region_name":"7","id":"rs1361567414","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140518931,"source":"dbSNP","strand":1,"feature_type":"variation","end":140518934,"alleles":["GAGG","G"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140518933,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GGGGG","GGGG"],"end":140518937,"seq_region_name":"7","id":"rs949126697","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1383153595","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140518934,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140518934},{"end":140518936,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140518936,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1418421370"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1381880335","end":140518937,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140518937,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140518938,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140518938,"source":"dbSNP","id":"rs1407808047","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140518948,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","T"],"end":140518948,"seq_region_name":"7","id":"rs1157508393","clinical_significance":[]},{"id":"rs1324399886","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140518962,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140518962,"source":"dbSNP"},{"id":"rs1795756144","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140518964,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140518964},{"source":"dbSNP","start":140518968,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140518968,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs559459242","seq_region_name":"7"},{"id":"rs905029754","seq_region_name":"7","clinical_significance":[],"start":140518972,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140518972,"strand":1,"feature_type":"variation"},{"alleles":["G","-"],"end":140518985,"strand":1,"feature_type":"variation","start":140518985,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795756485","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795756567","clinical_significance":[],"strand":1,"feature_type":"variation","end":140518987,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140518987,"source":"dbSNP"},{"start":140518989,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C","G"],"end":140518989,"strand":1,"feature_type":"variation","id":"rs1490142895","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795756801","end":140518992,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140518992,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563112287","source":"dbSNP","start":140519003,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140519003,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1263653900","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519004,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140519004},{"id":"rs578037670","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140519005,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519005,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519007,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140519007,"clinical_significance":[],"seq_region_name":"7","id":"rs1445245084"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1283409284","feature_type":"variation","strand":1,"alleles":["A","T"],"end":140519010,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519010},{"alleles":["C","T"],"end":140519018,"feature_type":"variation","strand":1,"source":"dbSNP","start":140519018,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1219935153"},{"seq_region_name":"7","id":"rs1795757516","clinical_significance":[],"alleles":["T","C"],"end":140519020,"strand":1,"feature_type":"variation","start":140519020,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795757635","clinical_significance":[],"strand":1,"feature_type":"variation","end":140519022,"alleles":["A","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519022,"source":"dbSNP"},{"id":"rs150338345","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140519026,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519026,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519027,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140519027,"seq_region_name":"7","id":"rs1795757825","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1347172512","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519029,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140519029},{"clinical_significance":[],"id":"rs1281686428","seq_region_name":"7","end":140519032,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140519032,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140519033,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519033,"clinical_significance":[],"seq_region_name":"7","id":"rs1223120410"},{"start":140519034,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140519034,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1231124338","clinical_significance":[]},{"seq_region_name":"7","id":"rs1021687946","clinical_significance":[],"start":140519037,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140519037,"strand":1,"feature_type":"variation"},{"id":"rs563622554","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519038,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140519038},{"source":"dbSNP","start":140519040,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140519040,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795758596","seq_region_name":"7"},{"end":140519045,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140519045,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs887022381"},{"seq_region_name":"7","id":"rs1242841261","clinical_significance":[],"strand":1,"feature_type":"variation","end":140519048,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519048,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs562726491","alleles":["G","A","C"],"end":140519049,"feature_type":"variation","strand":1,"source":"dbSNP","start":140519049,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs977442451","clinical_significance":[],"alleles":["A","C","G"],"end":140519052,"strand":1,"feature_type":"variation","start":140519052,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1019588170","alleles":["C","T"],"end":140519055,"feature_type":"variation","strand":1,"source":"dbSNP","start":140519055,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140519057,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140519057,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1423848750"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795759273","source":"dbSNP","start":140519065,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140519065,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519071,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140519071,"seq_region_name":"7","id":"rs1195601958","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795759453","feature_type":"variation","strand":1,"end":140519076,"alleles":["CTCT","CT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519073},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140519075,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519075,"source":"dbSNP","id":"rs928809160","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519076,"feature_type":"variation","strand":1,"end":140519076,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130441578"},{"seq_region_name":"7","id":"rs901158048","clinical_significance":[],"strand":1,"feature_type":"variation","end":140519088,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519088,"source":"dbSNP"},{"source":"dbSNP","start":140519089,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140519089,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795759728","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795759830","clinical_significance":[],"start":140519091,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140519091,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs530971340","clinical_significance":[],"strand":1,"feature_type":"variation","end":140519092,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519092,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs190331642","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519094,"feature_type":"variation","strand":1,"end":140519094,"alleles":["C","G","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519095,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140519095,"id":"rs968950810","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","A"],"end":140519097,"strand":1,"feature_type":"variation","start":140519097,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1261354509","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs117937485","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519102,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140519102},{"strand":1,"feature_type":"variation","end":140519108,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519108,"source":"dbSNP","seq_region_name":"7","id":"rs1795760529","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795760688","clinical_significance":[],"start":140519110,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140519110,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140519113,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519113,"clinical_significance":[],"seq_region_name":"7","id":"rs1318911069"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795760990","source":"dbSNP","start":140519115,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140519115,"feature_type":"variation","strand":1},{"start":140519116,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140519116,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs916134272","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140519118,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519118,"clinical_significance":[],"seq_region_name":"7","id":"rs182902935"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519119,"source":"dbSNP","strand":1,"feature_type":"variation","end":140519119,"alleles":["C","A","T"],"id":"rs1048107320","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140519120,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519120,"source":"dbSNP","id":"rs527816849","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795761809","seq_region_name":"7","end":140519126,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140519126,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519128,"feature_type":"variation","strand":1,"end":140519128,"alleles":["C","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs546594088"},{"source":"dbSNP","start":140519131,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140519131,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795762122"},{"seq_region_name":"7","id":"rs1795762282","clinical_significance":[],"strand":1,"feature_type":"variation","end":140519132,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519132,"source":"dbSNP"},{"alleles":["C","T"],"end":140519133,"strand":1,"feature_type":"variation","start":140519133,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1404462866","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795762493","source":"dbSNP","start":140519134,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140519134,"feature_type":"variation","strand":1},{"alleles":["G","T"],"end":140519138,"strand":1,"feature_type":"variation","start":140519138,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs2130441803","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585534850","feature_type":"variation","strand":1,"end":140519139,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519139},{"start":140519144,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140519144,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585534862","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140519145,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519145,"clinical_significance":[],"seq_region_name":"7","id":"rs1334161222"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130441850","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140519146,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519146},{"start":140519149,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140519149,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1468790962","clinical_significance":[]},{"start":140519150,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140519150,"alleles":["C","A","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs10267882","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1040779096","alleles":["A","G"],"end":140519157,"feature_type":"variation","strand":1,"source":"dbSNP","start":140519157,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519159,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140519159,"clinical_significance":[],"seq_region_name":"7","id":"rs1408064440"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519160,"source":"dbSNP","strand":1,"feature_type":"variation","end":140519160,"alleles":["C","T"],"seq_region_name":"7","id":"rs1795763394","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs980524346","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519162,"feature_type":"variation","strand":1,"end":140519162,"alleles":["C","A","T"]},{"seq_region_name":"7","id":"rs901047488","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519163,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140519163},{"seq_region_name":"7","id":"rs1795763733","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519165,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140519165},{"seq_region_name":"7","id":"rs1795763833","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519166,"source":"dbSNP","strand":1,"feature_type":"variation","end":140519166,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1563112440","clinical_significance":[],"strand":1,"feature_type":"variation","end":140519167,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519167,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["TA","-"],"end":140519169,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519168,"source":"dbSNP","seq_region_name":"7","id":"rs1563112444","clinical_significance":[]},{"seq_region_name":"7","id":"rs1241153195","clinical_significance":[],"alleles":["TACTG","-"],"end":140519172,"strand":1,"feature_type":"variation","start":140519168,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["TACTGG","C"],"end":140519173,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519168,"source":"dbSNP","seq_region_name":"7","id":"rs796374776","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795764321","clinical_significance":[],"alleles":["T","TT"],"end":140519171,"strand":1,"feature_type":"variation","start":140519171,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140519173,"alleles":["TGG","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519171,"source":"dbSNP","id":"rs1458174220","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs779860919","end":140519172,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140519172,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["G","C"],"end":140519173,"feature_type":"variation","strand":1,"source":"dbSNP","start":140519173,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs926352653"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1028271328","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140519175,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519175},{"clinical_significance":[],"id":"rs1260312578","seq_region_name":"7","source":"dbSNP","start":140519176,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140519176,"feature_type":"variation","strand":1},{"id":"rs538851218","seq_region_name":"7","clinical_significance":[],"start":140519177,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140519177,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1307079117","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140519179,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519179,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1393103850","clinical_significance":[],"start":140519180,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140519180,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1291046980","feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140519181,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519181},{"end":140519184,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140519184,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795765121","clinical_significance":[]},{"clinical_significance":[],"id":"rs1048684722","seq_region_name":"7","alleles":["T","C"],"end":140519187,"feature_type":"variation","strand":1,"source":"dbSNP","start":140519187,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1795765611","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["TTTTTT","TTTTTTT"],"end":140519192,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519187,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140519188,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519188,"clinical_significance":[],"id":"rs908343270","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795765894","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519193,"feature_type":"variation","strand":1,"end":140519193,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795766041","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140519194,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519194},{"id":"rs1795766175","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140519195,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519195,"source":"dbSNP"},{"start":140519199,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140519199,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs893696520","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519203,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140519203,"clinical_significance":[],"seq_region_name":"7","id":"rs561184161"},{"clinical_significance":[],"id":"rs1376984952","seq_region_name":"7","feature_type":"variation","strand":1,"end":140519204,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519204},{"alleles":["C","A","G"],"end":140519210,"feature_type":"variation","strand":1,"source":"dbSNP","start":140519210,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1040901595"},{"end":140519218,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140519218,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130442165"},{"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140519219,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519219,"source":"dbSNP","id":"rs1795766572","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs531747285","clinical_significance":[],"end":140519225,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140519225,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140519232,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140519232,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1460162583"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795766879","feature_type":"variation","strand":1,"end":140519238,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519238},{"clinical_significance":[],"seq_region_name":"7","id":"rs6464818","alleles":["A","G"],"end":140519244,"feature_type":"variation","strand":1,"source":"dbSNP","start":140519244,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1795767145","seq_region_name":"7","end":140519245,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140519245,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1165256630","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140519249,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519249},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140519252,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519252,"clinical_significance":[],"id":"rs1406826204","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1795767415","seq_region_name":"7","feature_type":"variation","strand":1,"end":140519253,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519253},{"seq_region_name":"7","id":"rs1795767517","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519253,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GTAAGT","GT"],"end":140519258},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519255,"feature_type":"variation","strand":1,"end":140519255,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795767598"},{"alleles":["A","G"],"end":140519256,"strand":1,"feature_type":"variation","start":140519256,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1383353362","clinical_significance":[]},{"clinical_significance":[],"id":"rs1245959210","seq_region_name":"7","source":"dbSNP","start":140519262,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","AAA"],"end":140519262,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs776273723","seq_region_name":"7","feature_type":"variation","strand":1,"end":140519263,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519263},{"source":"dbSNP","start":140519264,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140519264,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs747691354","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795768086","clinical_significance":[],"start":140519271,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140519271,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1049841961","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519274,"feature_type":"variation","strand":1,"end":140519274,"alleles":["T","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs537071777","end":140519285,"alleles":["T","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140519285,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1247463671","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519290,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140519290},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130442329","source":"dbSNP","start":140519295,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140519295,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1224305960","feature_type":"variation","strand":1,"end":140519296,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519296},{"seq_region_name":"7","id":"rs960262507","clinical_significance":[],"start":140519298,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140519298,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140519299,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519299,"source":"dbSNP","seq_region_name":"7","id":"rs992046045","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140519300,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519300,"source":"dbSNP","id":"rs1795768791","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","-"],"end":140519307,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519307,"source":"dbSNP","id":"rs1795768890","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","C"],"end":140519308,"feature_type":"variation","strand":1,"source":"dbSNP","start":140519308,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs555371816"},{"clinical_significance":[],"seq_region_name":"7","id":"rs573998262","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519315,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140519315},{"seq_region_name":"7","id":"rs534868771","clinical_significance":[],"start":140519316,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","T"],"end":140519316,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140519317,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140519317,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs552990752"},{"clinical_significance":[],"seq_region_name":"7","id":"rs577808334","feature_type":"variation","strand":1,"end":140519319,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519319},{"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140519321,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519321,"clinical_significance":[],"id":"rs931569054","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1308523501","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519326,"source":"dbSNP","strand":1,"feature_type":"variation","end":140519326,"alleles":["T","A"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519327,"source":"dbSNP","strand":1,"feature_type":"variation","end":140519327,"alleles":["G","T"],"id":"rs1795769673","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140519328,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140519328,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs544861275"},{"id":"rs1795769839","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140519330,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519330,"source":"dbSNP"},{"end":140519331,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140519331,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1389133985","clinical_significance":[]},{"id":"rs61156297","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140519333,"strand":1,"feature_type":"variation","start":140519333,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs763338583","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519334,"source":"dbSNP","strand":1,"feature_type":"variation","end":140519334,"alleles":["G","A"]},{"clinical_significance":[],"id":"rs1795770212","seq_region_name":"7","source":"dbSNP","start":140519339,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140519339,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140519340,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519340,"clinical_significance":[],"seq_region_name":"7","id":"rs939666866"},{"source":"dbSNP","start":140519341,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140519341,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130442495"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1363474454","source":"dbSNP","start":140519342,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140519342,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795770486","feature_type":"variation","strand":1,"end":140519343,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519343},{"seq_region_name":"7","id":"rs575309745","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140519344,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519344,"source":"dbSNP"},{"seq_region_name":"7","id":"rs900907468","clinical_significance":[],"alleles":["G","A","C"],"end":140519353,"strand":1,"feature_type":"variation","start":140519353,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130442541","source":"dbSNP","start":140519358,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140519358,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795770802","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519359,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140519359},{"id":"rs145006736","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140519360,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519360,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140519361,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519361,"source":"dbSNP","id":"rs1795770999","seq_region_name":"7","clinical_significance":[]},{"end":140519367,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140519367,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130442576","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130442582","clinical_significance":[],"start":140519368,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140519368,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"end":140519370,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140519370,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs73485763","clinical_significance":[]},{"seq_region_name":"7","id":"rs1157046115","clinical_significance":[],"end":140519372,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140519372,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140519373,"alleles":["T","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519373,"clinical_significance":[],"id":"rs528762061","seq_region_name":"7"},{"id":"rs1460083017","seq_region_name":"7","clinical_significance":[],"start":140519377,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140519377,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140519378,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140519378,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795771476"},{"clinical_significance":[],"id":"rs980429630","seq_region_name":"7","alleles":["T","A"],"end":140519382,"feature_type":"variation","strand":1,"source":"dbSNP","start":140519382,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140519385,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140519385,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs893605456","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519386,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140519386,"seq_region_name":"7","id":"rs1795771740","clinical_significance":[]},{"alleles":["G","A"],"end":140519389,"strand":1,"feature_type":"variation","start":140519389,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795771823","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795771942","clinical_significance":[],"strand":1,"feature_type":"variation","end":140519395,"alleles":["AA","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519394,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1193131014","seq_region_name":"7","end":140519405,"alleles":["AAGACAGCAAGA","AAGA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140519394,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140519395,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140519395,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795772115","clinical_significance":[]},{"clinical_significance":[],"id":"rs540966223","seq_region_name":"7","end":140519400,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140519400,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs372921156","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519401,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140519401},{"end":140519402,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140519402,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1268638307"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795772479","alleles":["A","G"],"end":140519403,"feature_type":"variation","strand":1,"source":"dbSNP","start":140519403,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1042281099","feature_type":"variation","strand":1,"end":140519408,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519408},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140519409,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519409,"source":"dbSNP","seq_region_name":"7","id":"rs1795772640","clinical_significance":[]},{"end":140519410,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140519410,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1217719724","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs571880396","clinical_significance":[],"alleles":["C","G","T"],"end":140519411,"strand":1,"feature_type":"variation","start":140519411,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519412,"source":"dbSNP","strand":1,"feature_type":"variation","end":140519412,"alleles":["G","A","T"],"seq_region_name":"7","id":"rs769250142","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795773040","feature_type":"variation","strand":1,"end":140519415,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519415},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519417,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140519417,"id":"rs1236313915","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140519422,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519422,"clinical_significance":[],"seq_region_name":"7","id":"rs1315809885"},{"feature_type":"variation","strand":1,"end":140519423,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519423,"clinical_significance":[],"seq_region_name":"7","id":"rs1301616286"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1224980941","feature_type":"variation","strand":1,"end":140519425,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519425},{"start":140519431,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140519431,"alleles":["T","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795773526","clinical_significance":[]},{"clinical_significance":[],"id":"rs1373207880","seq_region_name":"7","end":140519439,"alleles":["GGGGG","GGGG"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140519435,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["G","A"],"end":140519437,"strand":1,"feature_type":"variation","start":140519437,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795773610","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585535525","clinical_significance":[],"end":140519440,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140519440,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140519443,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140519443,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs998797690","clinical_significance":[]},{"clinical_significance":[],"id":"rs1035801423","seq_region_name":"7","feature_type":"variation","strand":1,"end":140519444,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519444},{"end":140519448,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140519448,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs188768687","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140519451,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519451,"clinical_significance":[],"id":"rs1353896390","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140519453,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519453,"clinical_significance":[],"seq_region_name":"7","id":"rs1795774399"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519456,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140519456,"clinical_significance":[],"id":"rs769014574","seq_region_name":"7"},{"start":140519462,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140519462,"strand":1,"feature_type":"variation","id":"rs1585535590","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519469,"source":"dbSNP","strand":1,"feature_type":"variation","end":140519469,"alleles":["C","T"],"seq_region_name":"7","id":"rs550873152","clinical_significance":[]},{"start":140519470,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140519470,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs763410985","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140519472,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519472,"clinical_significance":[],"seq_region_name":"7","id":"rs569754998"},{"source":"dbSNP","start":140519479,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140519479,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585535637"},{"id":"rs1359798509","seq_region_name":"7","clinical_significance":[],"alleles":["AGGAGG","AGG"],"end":140519485,"strand":1,"feature_type":"variation","start":140519480,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519484,"feature_type":"variation","strand":1,"end":140519484,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1479579542"},{"seq_region_name":"7","id":"rs1178601106","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519484,"source":"dbSNP","strand":1,"feature_type":"variation","end":140519485,"alleles":["GG","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1428807610","source":"dbSNP","start":140519485,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140519485,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140519494,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519494,"clinical_significance":[],"seq_region_name":"7","id":"rs1278376849"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140519497,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519497,"source":"dbSNP","id":"rs1012971689","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795775536","source":"dbSNP","start":140519504,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140519504,"feature_type":"variation","strand":1},{"end":140519506,"alleles":["G","C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140519506,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs530585230"},{"seq_region_name":"7","id":"rs1795775752","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519507,"source":"dbSNP","strand":1,"feature_type":"variation","end":140519507,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1585535716","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["CCC","CC","CCCC"],"end":140519509,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519507,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1023564456","seq_region_name":"7","end":140519510,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140519510,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs539076024","clinical_significance":[],"end":140519512,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140519512,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519513,"source":"dbSNP","strand":1,"feature_type":"variation","end":140519513,"alleles":["G","A"],"seq_region_name":"7","id":"rs1205048667","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519519,"feature_type":"variation","strand":1,"end":140519519,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs939824036"},{"start":140519520,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140519520,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1256079800","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795776451","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140519524,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519524},{"alleles":["G","A"],"end":140519525,"feature_type":"variation","strand":1,"source":"dbSNP","start":140519525,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1040976490"},{"end":140519529,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140519529,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795776640"},{"clinical_significance":[],"id":"rs1321003072","seq_region_name":"7","feature_type":"variation","strand":1,"end":140519530,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519530},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795776821","feature_type":"variation","strand":1,"alleles":["T","A"],"end":140519534,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519534},{"clinical_significance":[],"seq_region_name":"7","id":"rs1196171913","source":"dbSNP","start":140519536,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140519536,"alleles":["T","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs551390715","source":"dbSNP","start":140519543,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140519543,"alleles":["C","T"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140519544,"alleles":["G","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519544,"clinical_significance":[],"seq_region_name":"7","id":"rs1483528356"},{"seq_region_name":"7","id":"rs922522144","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140519545,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519545,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1795777334","seq_region_name":"7","feature_type":"variation","strand":1,"end":140519547,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519547},{"clinical_significance":[],"seq_region_name":"7","id":"rs1293416549","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519554,"feature_type":"variation","strand":1,"end":140519554,"alleles":["G","A","C"]},{"seq_region_name":"7","id":"rs1379711587","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519559,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140519559},{"clinical_significance":[],"id":"rs1338816415","seq_region_name":"7","end":140519560,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140519560,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140519562,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140519562,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs932679862"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795777875","end":140519565,"alleles":["CC","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140519564,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140519565,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519565,"clinical_significance":[],"seq_region_name":"7","id":"rs112251962"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519566,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140519566,"seq_region_name":"7","id":"rs1253823692","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795778242","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519571,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140519571},{"end":140519573,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140519573,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585535879"},{"seq_region_name":"7","id":"rs1795778417","clinical_significance":[],"start":140519574,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140519574,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140519577,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519577,"source":"dbSNP","id":"rs984413767","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","A"],"end":140519578,"strand":1,"feature_type":"variation","start":140519578,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs904492767","clinical_significance":[]},{"seq_region_name":"7","id":"rs1424933789","clinical_significance":[],"end":140519582,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140519582,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519588,"feature_type":"variation","strand":1,"alleles":["GCTCAGAGGCACACAGGCTGGGC","GCTCAGAGGCACACAGGCTGGGCGCTCAGAGGCACACAGGCTGGGC"],"end":140519610,"clinical_significance":[],"seq_region_name":"7","id":"rs770752162"},{"clinical_significance":[],"id":"rs1317746308","seq_region_name":"7","source":"dbSNP","start":140519590,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140519590,"alleles":["T","-"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1184958054","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140519594,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519594,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519595,"feature_type":"variation","strand":1,"end":140519595,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795778963"},{"source":"dbSNP","start":140519597,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["CACACA","CACA"],"end":140519602,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs776241025"},{"id":"rs773091139","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519601,"source":"dbSNP","strand":1,"feature_type":"variation","end":140519601,"alleles":["C","T"]},{"feature_type":"variation","strand":1,"end":140519603,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519603,"clinical_significance":[],"seq_region_name":"7","id":"rs908788988"},{"start":140519604,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140519604,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1224970302","clinical_significance":[]},{"seq_region_name":"7","id":"rs1217206264","clinical_significance":[],"alleles":["T","C"],"end":140519606,"strand":1,"feature_type":"variation","start":140519606,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs746814060","alleles":["C","G","T"],"end":140519612,"feature_type":"variation","strand":1,"source":"dbSNP","start":140519612,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795779576","clinical_significance":[],"alleles":["C","T"],"end":140519613,"strand":1,"feature_type":"variation","start":140519613,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519615,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140519615,"clinical_significance":[],"seq_region_name":"7","id":"rs372325499"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130443378","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140519616,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519616},{"seq_region_name":"7","id":"rs1340965269","clinical_significance":[],"start":140519619,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140519619,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"alleles":["C","G","T"],"end":140519621,"feature_type":"variation","strand":1,"source":"dbSNP","start":140519621,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs759170730"},{"seq_region_name":"7","id":"rs534591251","clinical_significance":[],"end":140519622,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140519622,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1249404699","clinical_significance":[],"alleles":["GGGG","GGGGG"],"end":140519625,"strand":1,"feature_type":"variation","start":140519622,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_donor_region_variant"},{"start":140519623,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140519623,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795780305","clinical_significance":[]},{"id":"rs763477958","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140519624,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"splice_region_variant","start":140519624,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"splice_region_variant","start":140519625,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140519625,"id":"rs764611339","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"splice_donor_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519626,"feature_type":"variation","strand":1,"end":140519626,"alleles":["C","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs751868425"},{"id":"rs12538386","seq_region_name":"7","clinical_significance":[],"start":140519627,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_donor_5th_base_variant","end":140519627,"alleles":["C","A","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1563112759","clinical_significance":[],"end":140519632,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140519632,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"alleles":["A","C"],"end":140519634,"strand":1,"feature_type":"variation","start":140519634,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs1445573220","clinical_significance":[]},{"end":140519635,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140519635,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795781192"},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519638,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140519638,"clinical_significance":["uncertain significance"],"id":"rs373925432","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140519639,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140519639,"id":"rs750619110","seq_region_name":"7","clinical_significance":["uncertain significance"]},{"alleles":["G","A"],"end":140519645,"strand":1,"feature_type":"variation","start":140519645,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","seq_region_name":"7","id":"rs1479310833","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140519648,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519648,"clinical_significance":[],"seq_region_name":"7","id":"rs756328923"},{"clinical_significance":[],"seq_region_name":"7","id":"rs780137278","source":"dbSNP","start":140519652,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140519652,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795781823","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519656,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140519656},{"seq_region_name":"7","id":"rs1795781907","clinical_significance":[],"end":140519658,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140519658,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140519659,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140519659,"seq_region_name":"7","id":"rs749345443","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140519660,"source":"dbSNP","strand":1,"feature_type":"variation","end":140519660,"alleles":["G","A","T"],"seq_region_name":"7","id":"rs375723849","clinical_significance":[]},{"seq_region_name":"7","id":"rs777857876","clinical_significance":[],"alleles":["C","A","T"],"end":140519661,"strand":1,"feature_type":"variation","start":140519661,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"feature_type":"variation","strand":1,"end":140519663,"alleles":["G","C"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519663,"clinical_significance":[],"id":"rs2130443581","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1024601972","clinical_significance":[],"start":140519665,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140519665,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1317415805","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140519667,"source":"dbSNP","strand":1,"feature_type":"variation","end":140519667,"alleles":["T","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs906095259","end":140519668,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140519668,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"id":"rs747008356","seq_region_name":"7","clinical_significance":[],"end":140519675,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140519675,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant"},{"consequence_type":"frameshift_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519675,"feature_type":"variation","strand":1,"alleles":["GGGG","GGGGG"],"end":140519678,"clinical_significance":[],"seq_region_name":"7","id":"rs35301689"},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140519676,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140519676,"seq_region_name":"7","id":"rs1443074552","clinical_significance":[]},{"seq_region_name":"7","id":"rs1301324117","clinical_significance":[],"start":140519677,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140519677,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140519680,"source":"dbSNP","strand":1,"feature_type":"variation","end":140519680,"alleles":["G","A"],"id":"rs770835290","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140519681,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140519681,"seq_region_name":"7","id":"rs776619198","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795783399","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140519682,"source":"dbSNP","strand":1,"feature_type":"variation","end":140519682,"alleles":["G","A"]},{"strand":1,"feature_type":"variation","end":140519689,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140519689,"source":"dbSNP","seq_region_name":"7","id":"rs1795783504","clinical_significance":[]},{"source":"dbSNP","start":140519690,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140519690,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs370003015"},{"source":"dbSNP","start":140519695,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140519695,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs769364711"},{"source":"dbSNP","start":140519696,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140519696,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1204881174","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140519697,"source":"dbSNP","strand":1,"feature_type":"variation","end":140519697,"alleles":["T","C"],"seq_region_name":"7","id":"rs1795783930","clinical_significance":[]},{"start":140519699,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","alleles":["G","A"],"end":140519699,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795784034","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140519701,"source":"dbSNP","strand":1,"feature_type":"variation","end":140519701,"alleles":["C","A","T"],"id":"rs1795784132","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs762385988","source":"dbSNP","start":140519703,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140519703,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795784386","consequence_type":"stop_gained","assembly_name":"GRCh38","source":"dbSNP","start":140519704,"feature_type":"variation","strand":1,"end":140519704,"alleles":["G","A"]},{"start":140519704,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"frameshift_variant","alleles":["GG","G"],"end":140519705,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795784461","clinical_significance":[]},{"id":"rs1795784569","seq_region_name":"7","clinical_significance":[],"alleles":["C","A","G"],"end":140519714,"strand":1,"feature_type":"variation","start":140519714,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant"},{"clinical_significance":[],"id":"rs1795784687","seq_region_name":"7","alleles":["A","C"],"end":140519715,"feature_type":"variation","strand":1,"source":"dbSNP","start":140519715,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1247919688","feature_type":"variation","strand":1,"end":140519717,"alleles":["A","G"],"consequence_type":"splice_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519717},{"seq_region_name":"7","id":"rs1195059125","clinical_significance":[],"strand":1,"feature_type":"variation","end":140519725,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"splice_region_variant","start":140519725,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"splice_region_variant","start":140519726,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140519726,"seq_region_name":"7","id":"rs138801925","clinical_significance":[]},{"id":"rs1795785085","seq_region_name":"7","clinical_significance":[],"start":140519733,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_polypyrimidine_tract_variant","end":140519733,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140519734,"consequence_type":"splice_polypyrimidine_tract_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519734,"clinical_significance":[],"id":"rs774839406","seq_region_name":"7"},{"seq_region_name":"7","id":"rs2130443829","clinical_significance":[],"strand":1,"feature_type":"variation","end":140519737,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519737,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1358561212","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519738,"source":"dbSNP","strand":1,"feature_type":"variation","end":140519738,"alleles":["C","T"]},{"feature_type":"variation","strand":1,"end":140519743,"alleles":["A","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519743,"clinical_significance":[],"id":"rs762369000","seq_region_name":"7"},{"id":"rs767832417","seq_region_name":"7","clinical_significance":[],"start":140519745,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140519745,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1795785571","seq_region_name":"7","feature_type":"variation","strand":1,"end":140519747,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519747},{"clinical_significance":[],"id":"rs1795785663","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519748,"feature_type":"variation","strand":1,"end":140519748,"alleles":["A","G"]},{"id":"rs1795785749","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140519754,"strand":1,"feature_type":"variation","start":140519754,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140519759,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140519759,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795785844","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs758420881","clinical_significance":[],"strand":1,"feature_type":"variation","end":140519761,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519761,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795786033","clinical_significance":[],"alleles":["G","A"],"end":140519762,"strand":1,"feature_type":"variation","start":140519762,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519765,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140519765,"seq_region_name":"7","id":"rs1453203066","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795786220","source":"dbSNP","start":140519769,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140519769,"alleles":["T","C"],"feature_type":"variation","strand":1},{"id":"rs750779329","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140519770,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519770,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1241213855","end":140519772,"alleles":["AAA","AA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140519770,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585536386","alleles":["A","T"],"end":140519771,"feature_type":"variation","strand":1,"source":"dbSNP","start":140519771,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1334257621","clinical_significance":[],"start":140519773,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140519773,"strand":1,"feature_type":"variation"},{"id":"rs1328402770","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519775,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140519775},{"alleles":["C","T"],"end":140519779,"strand":1,"feature_type":"variation","start":140519779,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs2130443979","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140519784,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140519784,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795786747"},{"alleles":["C","T"],"end":140519785,"feature_type":"variation","strand":1,"source":"dbSNP","start":140519785,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1341983091"},{"alleles":["C","T"],"end":140519787,"feature_type":"variation","strand":1,"source":"dbSNP","start":140519787,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs117228068"},{"alleles":["C","T"],"end":140519788,"feature_type":"variation","strand":1,"source":"dbSNP","start":140519788,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs984285505"},{"start":140519791,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140519791,"alleles":["A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795787127","clinical_significance":[]},{"seq_region_name":"7","id":"rs1424587194","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519792,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140519792},{"clinical_significance":[],"id":"rs1563112935","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519794,"feature_type":"variation","strand":1,"alleles":["AGAGAA","A"],"end":140519799},{"clinical_significance":[],"id":"rs1312193687","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519796,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140519796},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130444060","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140519797,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519797},{"seq_region_name":"7","id":"rs1795787511","clinical_significance":[],"alleles":["G","A","C"],"end":140519802,"strand":1,"feature_type":"variation","start":140519802,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs759990629","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519806,"source":"dbSNP","strand":1,"feature_type":"variation","end":140519806,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs1795787737","clinical_significance":[],"start":140519807,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140519807,"strand":1,"feature_type":"variation"},{"end":140519808,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140519808,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795787844","clinical_significance":[]},{"end":140519809,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140519809,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1158661977","clinical_significance":[]},{"clinical_significance":[],"id":"rs556845461","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519813,"feature_type":"variation","strand":1,"end":140519813,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1057444532","clinical_significance":[],"strand":1,"feature_type":"variation","end":140519814,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519814,"source":"dbSNP"},{"seq_region_name":"7","id":"rs11984104","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519817,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140519817},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795788227","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519819,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140519819},{"start":140519823,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140519823,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs767779220","clinical_significance":[]},{"source":"dbSNP","start":140519825,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140519825,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795788431"},{"alleles":["G","A"],"end":140519826,"feature_type":"variation","strand":1,"source":"dbSNP","start":140519826,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795788535"},{"seq_region_name":"7","id":"rs778280402","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519827,"source":"dbSNP","strand":1,"feature_type":"variation","end":140519827,"alleles":["C","T"]},{"start":140519828,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140519828,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795788736","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795788836","clinical_significance":[],"start":140519830,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140519830,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs2130444192","clinical_significance":[],"alleles":["T","G"],"end":140519831,"strand":1,"feature_type":"variation","start":140519831,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140519834,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140519834,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs976537866","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563112958","source":"dbSNP","start":140519835,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140519835,"alleles":["A","G"],"feature_type":"variation","strand":1},{"end":140519836,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140519836,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs575346403"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1270786460","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519837,"feature_type":"variation","strand":1,"end":140519837,"alleles":["A","C"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519841,"source":"dbSNP","strand":1,"feature_type":"variation","end":140519841,"alleles":["A","G","T"],"seq_region_name":"7","id":"rs1795789347","clinical_significance":[]},{"source":"dbSNP","start":140519843,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140519843,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs952892534","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs932581079","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140519845,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519845},{"feature_type":"variation","strand":1,"end":140519847,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519847,"clinical_significance":[],"seq_region_name":"7","id":"rs542663838"},{"strand":1,"feature_type":"variation","end":140519848,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519848,"source":"dbSNP","seq_region_name":"7","id":"rs141986916","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs961643114","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519850,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140519850},{"start":140519853,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140519853,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs977002894","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795789962","clinical_significance":[],"alleles":["AGGAGG","AGG"],"end":140519858,"strand":1,"feature_type":"variation","start":140519853,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519854,"source":"dbSNP","strand":1,"feature_type":"variation","end":140519854,"alleles":["G","C"],"seq_region_name":"7","id":"rs1795790056","clinical_significance":[]},{"end":140519857,"alleles":["G","C","T"],"strand":1,"feature_type":"variation","start":140519857,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs922262526","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795790255","clinical_significance":[],"strand":1,"feature_type":"variation","end":140519858,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519858,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1795790353","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["TTTT","TTT"],"end":140519862,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519859},{"start":140519863,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140519863,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795790453","clinical_significance":[]},{"seq_region_name":"7","id":"rs953734095","clinical_significance":[],"start":140519867,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140519867,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519873,"feature_type":"variation","strand":1,"end":140519873,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs935980872"},{"seq_region_name":"7","id":"rs985647960","clinical_significance":[],"end":140519879,"alleles":["T","A","C","G"],"strand":1,"feature_type":"variation","start":140519879,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519889,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140519889,"id":"rs1234261152","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140519891,"alleles":["C","A","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519891,"clinical_significance":[],"seq_region_name":"7","id":"rs1053645922"},{"id":"rs1795791194","seq_region_name":"7","clinical_significance":[],"start":140519894,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["ACCT","-"],"end":140519897,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519895,"feature_type":"variation","strand":1,"end":140519895,"alleles":["C","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1361791186"},{"feature_type":"variation","strand":1,"alleles":["CCTGTGCAGTAACTCC","CC"],"end":140519910,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519895,"clinical_significance":[],"seq_region_name":"7","id":"rs1404665357"},{"clinical_significance":[],"id":"rs950218846","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519903,"feature_type":"variation","strand":1,"end":140519903,"alleles":["G","A"]},{"strand":1,"feature_type":"variation","end":140519904,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519904,"source":"dbSNP","seq_region_name":"7","id":"rs914978603","clinical_significance":[]},{"start":140519905,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140519904,"alleles":["-","TTC"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795791597","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795791695","source":"dbSNP","start":140519905,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140519905,"alleles":["A","C"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140519909,"alleles":["CTC","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519907,"clinical_significance":[],"seq_region_name":"7","id":"rs1402006916"},{"clinical_significance":[],"id":"rs1795791898","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519909,"feature_type":"variation","strand":1,"end":140519909,"alleles":["C","A"]},{"seq_region_name":"7","id":"rs1382121745","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140519910,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519910,"source":"dbSNP"},{"id":"rs1795792099","seq_region_name":"7","clinical_significance":[],"start":140519912,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140519912,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519912,"feature_type":"variation","strand":1,"end":140519914,"alleles":["TTT","TT"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795792206"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1157415104","feature_type":"variation","strand":1,"end":140519915,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519915},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795792419","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519916,"feature_type":"variation","strand":1,"end":140519916,"alleles":["G","T"]},{"strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140519917,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519917,"source":"dbSNP","seq_region_name":"7","id":"rs946573470","clinical_significance":[]},{"start":140519920,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140519920,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130444534","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs572938870","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519923,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140519923},{"clinical_significance":[],"seq_region_name":"7","id":"rs977910211","feature_type":"variation","strand":1,"end":140519924,"alleles":["T","A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519924},{"id":"rs1795792822","seq_region_name":"7","clinical_significance":[],"alleles":["A","G"],"end":140519927,"strand":1,"feature_type":"variation","start":140519927,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140519928,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140519928,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs367768446","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","G"],"end":140519931,"strand":1,"feature_type":"variation","start":140519931,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795793007","clinical_significance":[]},{"alleles":["C","T"],"end":140519933,"feature_type":"variation","strand":1,"source":"dbSNP","start":140519933,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1197074360","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1479972034","clinical_significance":[],"start":140519935,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140519935,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["ATA","-"],"end":140519938,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519936,"clinical_significance":[],"seq_region_name":"7","id":"rs1434558785"},{"id":"rs1795793375","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519937,"source":"dbSNP","strand":1,"feature_type":"variation","end":140519937,"alleles":["T","C"]},{"start":140519939,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140519939,"alleles":["G","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs756204125","clinical_significance":[]},{"alleles":["A","T"],"end":140519944,"feature_type":"variation","strand":1,"source":"dbSNP","start":140519944,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795793591"},{"start":140519947,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140519947,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1299169657","clinical_significance":[]},{"seq_region_name":"7","id":"rs117447751","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519953,"source":"dbSNP","strand":1,"feature_type":"variation","end":140519953,"alleles":["T","C"]},{"alleles":["T","C"],"end":140519955,"feature_type":"variation","strand":1,"source":"dbSNP","start":140519955,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795793925"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1283652357","source":"dbSNP","start":140519959,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140519959,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1204336783","seq_region_name":"7","end":140519960,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140519960,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["A","C"],"end":140519963,"strand":1,"feature_type":"variation","start":140519963,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795794212","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs532666767","clinical_significance":[],"start":140519966,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140519966,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs758289423","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519967,"source":"dbSNP","strand":1,"feature_type":"variation","end":140519967,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795794497","alleles":["C","T"],"end":140519969,"feature_type":"variation","strand":1,"source":"dbSNP","start":140519969,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140519973,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140519973,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs948743705"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140519974,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519974,"source":"dbSNP","seq_region_name":"7","id":"rs1223321396","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140519977,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519977,"source":"dbSNP","seq_region_name":"7","id":"rs1044906178","clinical_significance":[]},{"end":140519978,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140519978,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs888514502","clinical_significance":[]},{"id":"rs1795794973","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140519979,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519979,"source":"dbSNP"},{"alleles":["C","T"],"end":140519983,"strand":1,"feature_type":"variation","start":140519983,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1429252957","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1326317006","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140519984,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140519984},{"source":"dbSNP","start":140519985,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140519985,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795795219"},{"strand":1,"feature_type":"variation","end":140519987,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140519987,"source":"dbSNP","seq_region_name":"7","id":"rs1795795296","clinical_significance":[]},{"end":140519993,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140519993,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795795408","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1387987605","source":"dbSNP","start":140519995,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140519995,"alleles":["C","T"],"feature_type":"variation","strand":1},{"alleles":["G","A"],"end":140519996,"feature_type":"variation","strand":1,"source":"dbSNP","start":140519996,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs568228155"},{"start":140519997,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140519997,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1407897760","clinical_significance":[]},{"source":"dbSNP","start":140519998,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140519998,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1015784366","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520000,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140520000,"id":"rs897295180","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795795917","seq_region_name":"7","source":"dbSNP","start":140520001,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140520001,"alleles":["G","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs998882207","clinical_significance":[],"start":140520002,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A","C"],"end":140520002,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs961100856","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520002,"feature_type":"variation","strand":1,"alleles":["TTTT","TTTTTT"],"end":140520005},{"id":"rs767005213","seq_region_name":"7","clinical_significance":[],"start":140520004,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140520004,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"id":"rs1795796316","seq_region_name":"7","clinical_significance":[],"end":140520008,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140520008,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1795796405","seq_region_name":"7","clinical_significance":[],"start":140520013,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140520013,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1287917358","clinical_significance":[],"start":140520016,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140520016,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1187981173","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140520017,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520017,"source":"dbSNP"},{"alleles":["A","C","T"],"end":140520019,"feature_type":"variation","strand":1,"source":"dbSNP","start":140520019,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs10277775"},{"seq_region_name":"7","id":"rs1029467823","clinical_significance":[],"start":140520027,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140520027,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1795797229","seq_region_name":"7","end":140520029,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140520029,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs953872454","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520031,"source":"dbSNP","strand":1,"feature_type":"variation","end":140520031,"alleles":["T","C"]},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140520032,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520032,"clinical_significance":[],"seq_region_name":"7","id":"rs1795797434"},{"strand":1,"feature_type":"variation","alleles":["GG","G"],"end":140520033,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520032,"source":"dbSNP","seq_region_name":"7","id":"rs1462684125","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1213960861","end":140520034,"alleles":["T","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140520034,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795797749","clinical_significance":[],"strand":1,"feature_type":"variation","end":140520036,"alleles":["GG","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520035,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1585537038","clinical_significance":[],"start":140520037,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140520037,"alleles":["T","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1241602633","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520038,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140520038},{"clinical_significance":[],"seq_region_name":"7","id":"rs985125060","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520040,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140520040},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520041,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140520041,"seq_region_name":"7","id":"rs1488869568","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140520042,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520042,"clinical_significance":[],"seq_region_name":"7","id":"rs1275590557"},{"clinical_significance":[],"seq_region_name":"7","id":"rs985786954","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520043,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140520043},{"seq_region_name":"7","id":"rs925882471","clinical_significance":[],"end":140520044,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140520044,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140520045,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520045,"source":"dbSNP","id":"rs1795798597","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520046,"feature_type":"variation","strand":1,"end":140520046,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1316310543"},{"alleles":["C","T"],"end":140520053,"feature_type":"variation","strand":1,"source":"dbSNP","start":140520053,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1192983890"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130445029","alleles":["C","G"],"end":140520056,"feature_type":"variation","strand":1,"source":"dbSNP","start":140520056,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1452820697","seq_region_name":"7","clinical_significance":[],"end":140520057,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140520057,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520058,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140520058,"clinical_significance":[],"seq_region_name":"7","id":"rs1251740242"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1334056356","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140520059,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520059},{"source":"dbSNP","start":140520061,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140520061,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1446846352"},{"strand":1,"feature_type":"variation","end":140520062,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520062,"source":"dbSNP","seq_region_name":"7","id":"rs1795799326","clinical_significance":[]},{"alleles":["G","C"],"end":140520064,"feature_type":"variation","strand":1,"source":"dbSNP","start":140520064,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795799438","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520066,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140520066,"seq_region_name":"7","id":"rs1795799549","clinical_significance":[]},{"seq_region_name":"7","id":"rs1354708784","clinical_significance":[],"alleles":["G","A"],"end":140520073,"strand":1,"feature_type":"variation","start":140520073,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1585537166","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140520074,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520074,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140520079,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520079,"source":"dbSNP","seq_region_name":"7","id":"rs1795799871","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520080,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140520080,"seq_region_name":"7","id":"rs1172292123","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520084,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140520084,"clinical_significance":[],"seq_region_name":"7","id":"rs1407978586"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795800151","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140520090,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520090},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795800253","alleles":["A","G"],"end":140520091,"feature_type":"variation","strand":1,"source":"dbSNP","start":140520091,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs530315564","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140520092,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520092},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140520094,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520094,"clinical_significance":[],"id":"rs1159710692","seq_region_name":"7"},{"source":"dbSNP","start":140520095,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140520095,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795800576"},{"clinical_significance":[],"seq_region_name":"7","id":"rs145646774","end":140520096,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140520096,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1399270737","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520101,"source":"dbSNP","strand":1,"feature_type":"variation","end":140520101,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1241372915","alleles":["G","A"],"end":140520102,"feature_type":"variation","strand":1,"source":"dbSNP","start":140520102,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795800999","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520109,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140520109},{"seq_region_name":"7","id":"rs1182990348","clinical_significance":[],"strand":1,"feature_type":"variation","end":140520110,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520110,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795801198","source":"dbSNP","start":140520120,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140520120,"feature_type":"variation","strand":1},{"end":140520121,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140520121,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795801302"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520123,"feature_type":"variation","strand":1,"end":140520123,"alleles":["G","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1481095558"},{"start":140520125,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140520125,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795801397","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs967781733","alleles":["A","G"],"end":140520126,"feature_type":"variation","strand":1,"source":"dbSNP","start":140520126,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795801605","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520129,"feature_type":"variation","strand":1,"end":140520129,"alleles":["C","T"]},{"id":"rs1795801693","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140520130,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520130,"source":"dbSNP"},{"seq_region_name":"7","id":"rs555461610","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","G","T"],"end":140520131,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520131,"source":"dbSNP"},{"seq_region_name":"7","id":"rs923780811","clinical_significance":[],"end":140520134,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140520134,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795802056","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520140,"feature_type":"variation","strand":1,"end":140520140,"alleles":["C","A"]},{"seq_region_name":"7","id":"rs950125525","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140520141,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520141,"source":"dbSNP"},{"start":140520147,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140520147,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130445279","clinical_significance":[]},{"seq_region_name":"7","id":"rs567354840","clinical_significance":[],"end":140520148,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140520148,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs906039717","seq_region_name":"7","clinical_significance":[],"end":140520156,"alleles":["AAAAAAA","AAAAAA","AAAAAAAA"],"strand":1,"feature_type":"variation","start":140520150,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140520155,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140520155,"strand":1,"feature_type":"variation","id":"rs1795802364","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs937517593","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520158,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140520158},{"alleles":["G","T"],"end":140520160,"feature_type":"variation","strand":1,"source":"dbSNP","start":140520160,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795802580"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140520161,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520161,"source":"dbSNP","seq_region_name":"7","id":"rs1795802677","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795802784","seq_region_name":"7","source":"dbSNP","start":140520162,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140520162,"feature_type":"variation","strand":1},{"end":140520164,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140520164,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795802885","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795802981","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520165,"source":"dbSNP","strand":1,"feature_type":"variation","end":140520165,"alleles":["G","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795803094","alleles":["G","C"],"end":140520170,"feature_type":"variation","strand":1,"source":"dbSNP","start":140520170,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["T","G"],"end":140520171,"feature_type":"variation","strand":1,"source":"dbSNP","start":140520171,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1438071204"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520173,"source":"dbSNP","strand":1,"feature_type":"variation","end":140520173,"alleles":["G","A"],"seq_region_name":"7","id":"rs1323293810","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1049818603","end":140520174,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140520174,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs888019581","clinical_significance":[],"strand":1,"feature_type":"variation","end":140520175,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520175,"source":"dbSNP"},{"start":140520178,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140520178,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1439832904","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1369541035","alleles":["G","A"],"end":140520179,"feature_type":"variation","strand":1,"source":"dbSNP","start":140520179,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1795803995","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140520192,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520192,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520194,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140520194,"seq_region_name":"7","id":"rs1447433219","clinical_significance":[]},{"seq_region_name":"7","id":"rs528122024","clinical_significance":[],"alleles":["C","A","T"],"end":140520198,"strand":1,"feature_type":"variation","start":140520198,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140520199,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520199,"source":"dbSNP","seq_region_name":"7","id":"rs7803669","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795804517","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140520200,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520200},{"seq_region_name":"7","id":"rs1585537350","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140520202,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520202,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520211,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140520211,"clinical_significance":[],"seq_region_name":"7","id":"rs2130445472"},{"seq_region_name":"7","id":"rs1795804736","clinical_significance":[],"end":140520214,"alleles":["GG","G"],"strand":1,"feature_type":"variation","start":140520213,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520214,"source":"dbSNP","strand":1,"feature_type":"variation","end":140520214,"alleles":["G","A"],"seq_region_name":"7","id":"rs1392548768","clinical_significance":[]},{"id":"rs376161086","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520216,"source":"dbSNP","strand":1,"feature_type":"variation","end":140520216,"alleles":["A","C","G"]},{"source":"dbSNP","start":140520217,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140520217,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795805099"},{"start":140520220,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140520220,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1163064477","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140520221,"alleles":["G","A","C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520221,"clinical_significance":[],"seq_region_name":"7","id":"rs753504509"},{"seq_region_name":"7","id":"rs1795805524","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520223,"source":"dbSNP","strand":1,"feature_type":"variation","end":140520223,"alleles":["T","C"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520228,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140520228,"clinical_significance":[],"seq_region_name":"7","id":"rs896801492"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795805764","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520229,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140520229},{"seq_region_name":"7","id":"rs1795805868","clinical_significance":[],"start":140520230,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140520230,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140520231,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520231,"clinical_significance":[],"seq_region_name":"7","id":"rs916490178"},{"strand":1,"feature_type":"variation","alleles":["GGG","GG"],"end":140520233,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520231,"source":"dbSNP","seq_region_name":"7","id":"rs1795806062","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520234,"feature_type":"variation","strand":1,"end":140520234,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1468057098"},{"seq_region_name":"7","id":"rs948754369","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520237,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140520237},{"seq_region_name":"7","id":"rs1044435803","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140520238,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520238,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1270060419","clinical_significance":[],"start":140520243,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140520243,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"alleles":["G","A"],"end":140520245,"strand":1,"feature_type":"variation","start":140520245,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130445605","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585537479","clinical_significance":[],"end":140520247,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140520247,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1235080204","clinical_significance":[],"start":140520250,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140520250,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140520252,"alleles":["G","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520252,"clinical_significance":[],"seq_region_name":"7","id":"rs1795806770"},{"clinical_significance":[],"id":"rs997892231","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520253,"feature_type":"variation","strand":1,"end":140520253,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs888420233","clinical_significance":[],"start":140520255,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140520255,"strand":1,"feature_type":"variation"},{"id":"rs1795807096","seq_region_name":"7","clinical_significance":[],"start":140520258,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140520258,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795807203","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520259,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140520259},{"seq_region_name":"7","id":"rs1468962192","clinical_significance":[],"start":140520262,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140520262,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1220235551","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140520263,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520263,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1176984292","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140520264,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520264,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795807600","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140520271,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520271},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520273,"feature_type":"variation","strand":1,"end":140520273,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795807693"},{"clinical_significance":[],"id":"rs1652557496","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140520275,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520275},{"seq_region_name":"7","id":"rs1795807783","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140520278,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520278,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520280,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140520280,"seq_region_name":"7","id":"rs2130445733","clinical_significance":[]},{"id":"rs1001582016","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140520287,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520287,"source":"dbSNP"},{"alleles":["A","G"],"end":140520289,"strand":1,"feature_type":"variation","start":140520289,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1029331253","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795808087","clinical_significance":[],"start":140520292,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140520292,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs369409314","alleles":["T","C","G"],"end":140520293,"feature_type":"variation","strand":1,"source":"dbSNP","start":140520293,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1221726772","seq_region_name":"7","clinical_significance":[],"start":140520296,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140520296,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs953913183","clinical_significance":[],"alleles":["A","T"],"end":140520297,"strand":1,"feature_type":"variation","start":140520297,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["C","T"],"end":140520298,"strand":1,"feature_type":"variation","start":140520298,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs2130445796","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1027672083","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520299,"feature_type":"variation","strand":1,"end":140520299,"alleles":["T","C"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520300,"feature_type":"variation","strand":1,"end":140520300,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1406754801"},{"start":140520301,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140520301,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1006721263","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1393141295","source":"dbSNP","start":140520302,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140520302,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140520304,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520304,"source":"dbSNP","seq_region_name":"7","id":"rs1363682451","clinical_significance":[]},{"seq_region_name":"7","id":"rs7803826","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","C","T"],"end":140520305,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520305,"source":"dbSNP"},{"seq_region_name":"7","id":"rs983717882","clinical_significance":[],"start":140520306,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140520306,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"id":"rs1795809372","seq_region_name":"7","clinical_significance":[],"alleles":["-","G"],"end":140520306,"strand":1,"feature_type":"variation","start":140520307,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs568755938","source":"dbSNP","start":140520307,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140520307,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["AAAAAAAAAAAAAAAA","AAAAAAAAAAAA","AAAAAAAAAAAAA","AAAAAAAAAAAAAA","AAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAA"],"end":140520322,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520307,"source":"dbSNP","id":"rs762064430","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140520308,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140520308,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1033365149"},{"seq_region_name":"7","id":"rs1487102130","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140520316,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520316,"source":"dbSNP"},{"clinical_significance":[],"id":"rs2130445927","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520319,"feature_type":"variation","strand":1,"end":140520318,"alleles":["-","G"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520320,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140520320,"id":"rs1390743918","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1261974998","clinical_significance":[],"start":140520321,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140520321,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"start":140520322,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140520322,"alleles":["A","C","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1328113609","clinical_significance":[]},{"seq_region_name":"7","id":"rs1212986786","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520323,"source":"dbSNP","strand":1,"feature_type":"variation","end":140520322,"alleles":["-","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520323,"feature_type":"variation","strand":1,"end":140520323,"alleles":["G","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs536026933"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795810776","feature_type":"variation","strand":1,"end":140520323,"alleles":["G","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520323},{"id":"rs1284578498","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520324,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140520324},{"seq_region_name":"7","id":"rs1263345218","clinical_significance":[],"end":140520325,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140520325,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs192485031","end":140520330,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140520330,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140520331,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520331,"clinical_significance":[],"seq_region_name":"7","id":"rs572977658"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140520334,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520334,"clinical_significance":[],"seq_region_name":"7","id":"rs1795811191"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520338,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140520338,"seq_region_name":"7","id":"rs1037114508","clinical_significance":[]},{"id":"rs897348352","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140520339,"strand":1,"feature_type":"variation","start":140520339,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1291612991","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520340,"source":"dbSNP","strand":1,"feature_type":"variation","end":140520340,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs74785633","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520347,"source":"dbSNP","strand":1,"feature_type":"variation","end":140520347,"alleles":["G","A"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520348,"source":"dbSNP","strand":1,"feature_type":"variation","end":140520348,"alleles":["G","T"],"seq_region_name":"7","id":"rs1456751845","clinical_significance":[]},{"clinical_significance":[],"id":"rs1014740217","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140520349,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520349},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563113320","source":"dbSNP","start":140520350,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140520350,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520351,"source":"dbSNP","strand":1,"feature_type":"variation","end":140520351,"alleles":["G","A"],"seq_region_name":"7","id":"rs1795812181","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520352,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140520352,"seq_region_name":"7","id":"rs2130446099","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140520361,"alleles":["GTGTCTGTG","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520353,"clinical_significance":[],"seq_region_name":"7","id":"rs1407159891"},{"seq_region_name":"7","id":"rs966395305","clinical_significance":[],"start":140520354,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140520354,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140520355,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520355,"source":"dbSNP","id":"rs1795812486","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130446156","alleles":["T","C"],"end":140520356,"feature_type":"variation","strand":1,"source":"dbSNP","start":140520356,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140520357,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140520357,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795812571","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1468620165","feature_type":"variation","strand":1,"end":140520359,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520359},{"id":"rs1585537909","seq_region_name":"7","clinical_significance":[],"end":140520361,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140520361,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs913238962","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520363,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140520363},{"clinical_significance":[],"id":"rs1795812970","seq_region_name":"7","end":140520366,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140520366,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","A","G","T"],"end":140520368,"feature_type":"variation","strand":1,"source":"dbSNP","start":140520368,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1171484085"},{"seq_region_name":"7","id":"rs971353881","clinical_significance":[],"start":140520370,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140520372,"alleles":["TTT","TTTT"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140520371,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140520371,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1260196223"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1030351057","feature_type":"variation","strand":1,"end":140520375,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520375},{"seq_region_name":"7","id":"rs1464046173","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520379,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140520379},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520380,"feature_type":"variation","strand":1,"end":140520380,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585537980"},{"id":"rs2130446270","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140520384,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520384,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795813707","source":"dbSNP","start":140520386,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140520386,"alleles":["T","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1199316581","feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140520390,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520390},{"source":"dbSNP","start":140520391,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140520391,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1320894475"},{"seq_region_name":"7","id":"rs890060744","clinical_significance":[],"strand":1,"feature_type":"variation","end":140520398,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520398,"source":"dbSNP"},{"alleles":["T","A"],"end":140520407,"strand":1,"feature_type":"variation","start":140520407,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795814132","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140520414,"alleles":["GCTTAG","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520409,"clinical_significance":[],"seq_region_name":"7","id":"rs1227830698"},{"seq_region_name":"7","id":"rs1007521783","clinical_significance":[],"start":140520413,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140520413,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1436565763","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140520414,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520414,"source":"dbSNP"},{"seq_region_name":"7","id":"rs2130446344","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140520416,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520416,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520418,"source":"dbSNP","strand":1,"feature_type":"variation","end":140520418,"alleles":["T","C"],"seq_region_name":"7","id":"rs1795814454","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795814551","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520422,"source":"dbSNP","strand":1,"feature_type":"variation","end":140520422,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795814711","alleles":["G","A"],"end":140520423,"feature_type":"variation","strand":1,"source":"dbSNP","start":140520423,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1309241777","source":"dbSNP","start":140520426,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140520426,"alleles":["T","A"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140520428,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520428,"source":"dbSNP","seq_region_name":"7","id":"rs1795814995","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795815137","clinical_significance":[],"alleles":["TGTGGAGGTGTGGAGG","TGTGGAGGTGTGGAGGTGTGGAGG"],"end":140520447,"strand":1,"feature_type":"variation","start":140520432,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140520434,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140520434,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130446392","clinical_significance":[]},{"end":140520438,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140520438,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130446397"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1204370895","end":140520439,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140520439,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs558645992","feature_type":"variation","strand":1,"end":140520447,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520447},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520453,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140520453,"clinical_significance":[],"seq_region_name":"7","id":"rs2130446417"},{"id":"rs1795815738","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520457,"source":"dbSNP","strand":1,"feature_type":"variation","end":140520457,"alleles":["T","C"]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140520458,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520458,"clinical_significance":[],"seq_region_name":"7","id":"rs1434546640"},{"seq_region_name":"7","id":"rs1585538065","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520460,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140520460},{"start":140520462,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140520462,"alleles":["A","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1021923564","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140520463,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520463,"clinical_significance":[],"seq_region_name":"7","id":"rs967647267"},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140520469,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520469,"source":"dbSNP","id":"rs1338714372","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130446471","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520470,"feature_type":"variation","strand":1,"end":140520470,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs937531273","clinical_significance":[],"alleles":["C","G"],"end":140520471,"strand":1,"feature_type":"variation","start":140520471,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["TT","-"],"end":140520473,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520472,"source":"dbSNP","seq_region_name":"7","id":"rs1795816372","clinical_significance":[]},{"source":"dbSNP","start":140520473,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140520473,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795816469","seq_region_name":"7"},{"seq_region_name":"7","id":"rs2130446516","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520475,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140520475},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520476,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140520476,"seq_region_name":"7","id":"rs2130446522","clinical_significance":[]},{"source":"dbSNP","start":140520478,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140520478,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs780889132"},{"clinical_significance":[],"seq_region_name":"7","id":"rs537163146","source":"dbSNP","start":140520479,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140520479,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130446553","feature_type":"variation","strand":1,"end":140520480,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520480},{"feature_type":"variation","strand":1,"end":140520481,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520481,"clinical_significance":[],"seq_region_name":"7","id":"rs2130446560"},{"end":140520482,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140520482,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130446572","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130446580","clinical_significance":[],"end":140520483,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140520483,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140520487,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520487,"clinical_significance":[],"id":"rs2130446590","seq_region_name":"7"},{"seq_region_name":"7","id":"rs2130446599","clinical_significance":[],"alleles":["C","A"],"end":140520492,"strand":1,"feature_type":"variation","start":140520492,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130446604","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520493,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140520493},{"start":140520494,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140520494,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130446615","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1463823843","source":"dbSNP","start":140520501,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140520501,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795816932","end":140520506,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140520506,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1371919760","seq_region_name":"7","clinical_significance":[],"end":140520513,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140520513,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520527,"feature_type":"variation","strand":1,"end":140520527,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1168498030"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1477897972","source":"dbSNP","start":140520528,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140520528,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140520530,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520530,"clinical_significance":[],"seq_region_name":"7","id":"rs1049217230"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795817513","alleles":["T","C"],"end":140520535,"feature_type":"variation","strand":1,"source":"dbSNP","start":140520535,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140520536,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520536,"source":"dbSNP","seq_region_name":"7","id":"rs1393616563","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520539,"source":"dbSNP","strand":1,"feature_type":"variation","end":140520539,"alleles":["T","C"],"seq_region_name":"7","id":"rs960854481","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140520541,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520541,"clinical_significance":[],"seq_region_name":"7","id":"rs991989911"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520542,"feature_type":"variation","strand":1,"end":140520542,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795817887"},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140520546,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520546,"clinical_significance":[],"id":"rs1585538180","seq_region_name":"7"},{"id":"rs1795818110","seq_region_name":"7","clinical_significance":[],"start":140520548,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140520548,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140520550,"alleles":["G","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520550,"clinical_significance":[],"seq_region_name":"7","id":"rs1440361539"},{"seq_region_name":"7","id":"rs1255026444","clinical_significance":[],"end":140520552,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140520552,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs577474342","seq_region_name":"7","clinical_significance":[],"alleles":["C","A"],"end":140520555,"strand":1,"feature_type":"variation","start":140520555,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140520561,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140520561,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1334691935","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795818846","feature_type":"variation","strand":1,"end":140520561,"alleles":["A","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520561},{"feature_type":"variation","strand":1,"end":140520564,"alleles":["G","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520564,"clinical_significance":[],"seq_region_name":"7","id":"rs1249601249"},{"alleles":["-","C"],"end":140520564,"feature_type":"variation","strand":1,"source":"dbSNP","start":140520565,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795819165"},{"strand":1,"feature_type":"variation","end":140520565,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520565,"source":"dbSNP","seq_region_name":"7","id":"rs544625534","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs563122298","feature_type":"variation","strand":1,"alleles":["TTTTTTTTTTTT","TTTTTTTTTT","TTTTTTTTTTT","TTTTTTTTTTTTT","TTTTTTTTTTTTTT"],"end":140520576,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520565},{"alleles":["T","C"],"end":140520566,"feature_type":"variation","strand":1,"source":"dbSNP","start":140520566,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1317290163"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795819648","end":140520567,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140520567,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520568,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140520568,"clinical_significance":[],"id":"rs1795819738","seq_region_name":"7"},{"id":"rs909345657","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520570,"source":"dbSNP","strand":1,"feature_type":"variation","end":140520570,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1340148351","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520572,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140520572},{"seq_region_name":"7","id":"rs77537767","clinical_significance":[],"alleles":["T","G"],"end":140520576,"strand":1,"feature_type":"variation","start":140520576,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520577,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140520577,"clinical_significance":[],"seq_region_name":"7","id":"rs1329786917"},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140520579,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520579,"source":"dbSNP","seq_region_name":"7","id":"rs1393559812","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520580,"feature_type":"variation","strand":1,"end":140520580,"alleles":["A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795820268"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520581,"feature_type":"variation","strand":1,"end":140520581,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1394800920"},{"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140520583,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520583,"source":"dbSNP","seq_region_name":"7","id":"rs1307741826","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1425883718","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520589,"feature_type":"variation","strand":1,"end":140520589,"alleles":["C","T"]},{"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140520590,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520590,"source":"dbSNP","seq_region_name":"7","id":"rs563166985","clinical_significance":[]},{"alleles":["T","C"],"end":140520594,"strand":1,"feature_type":"variation","start":140520594,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795820667","clinical_significance":[]},{"end":140520599,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140520599,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130446915"},{"source":"dbSNP","start":140520605,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140520605,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1164991462"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795820840","source":"dbSNP","start":140520607,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140520607,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1311334366","feature_type":"variation","strand":1,"end":140520609,"alleles":["A","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520609},{"end":140520611,"alleles":["T","A","G"],"strand":1,"feature_type":"variation","start":140520611,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585538315","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140520619,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520619,"source":"dbSNP","seq_region_name":"7","id":"rs1585538325","clinical_significance":[]},{"alleles":["C","T"],"end":140520624,"feature_type":"variation","strand":1,"source":"dbSNP","start":140520624,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795821195"},{"source":"dbSNP","start":140520628,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140520628,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1355057585","seq_region_name":"7"},{"seq_region_name":"7","id":"rs940973229","clinical_significance":[],"alleles":["C","T"],"end":140520630,"strand":1,"feature_type":"variation","start":140520630,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140520631,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140520631,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795821487","seq_region_name":"7"},{"alleles":["C","T"],"end":140520632,"strand":1,"feature_type":"variation","start":140520632,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130447020","clinical_significance":[]},{"end":140520637,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140520637,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1182062214","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520640,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140520640,"clinical_significance":[],"seq_region_name":"7","id":"rs1219392070"},{"seq_region_name":"7","id":"rs1036531613","clinical_significance":[],"start":140520641,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140520641,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520644,"feature_type":"variation","strand":1,"end":140520644,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795821891"},{"clinical_significance":[],"id":"rs1272016135","seq_region_name":"7","alleles":["C","T"],"end":140520646,"feature_type":"variation","strand":1,"source":"dbSNP","start":140520646,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520647,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140520647,"clinical_significance":[],"seq_region_name":"7","id":"rs1337458800"},{"start":140520651,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140520651,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs141896403","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140520656,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520656,"clinical_significance":[],"seq_region_name":"7","id":"rs2130447099"},{"clinical_significance":[],"seq_region_name":"7","id":"rs542419993","source":"dbSNP","start":140520661,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140520661,"alleles":["C","T"],"feature_type":"variation","strand":1},{"start":140520662,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140520662,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1293827142","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs747808595","end":140520663,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140520663,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520664,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140520664,"clinical_significance":[],"seq_region_name":"7","id":"rs1795822532"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520667,"feature_type":"variation","strand":1,"end":140520667,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795822604"},{"seq_region_name":"7","id":"rs1795822685","clinical_significance":[],"end":140520668,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140520668,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140520675,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140520675,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795822765","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795822861","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520676,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140520676},{"source":"dbSNP","start":140520678,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140520678,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1486888502","seq_region_name":"7"},{"alleles":["G","T"],"end":140520684,"strand":1,"feature_type":"variation","start":140520684,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1280154153","clinical_significance":[]},{"end":140520686,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140520686,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1209144791"},{"end":140520691,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140520691,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795823212","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140520699,"alleles":["-","TCAGG"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520700,"source":"dbSNP","seq_region_name":"7","id":"rs1795823303","clinical_significance":[]},{"alleles":["A","T"],"end":140520700,"feature_type":"variation","strand":1,"source":"dbSNP","start":140520700,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795823433"},{"clinical_significance":[],"seq_region_name":"7","id":"rs150664333","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520703,"feature_type":"variation","strand":1,"end":140520703,"alleles":["C","T"]},{"clinical_significance":[],"id":"rs752640680","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520704,"feature_type":"variation","strand":1,"end":140520704,"alleles":["G","A"]},{"id":"rs1795823924","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140520705,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520705,"source":"dbSNP"},{"id":"rs1370873328","seq_region_name":"7","clinical_significance":[],"start":140520706,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140520706,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1474765522","source":"dbSNP","start":140520707,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140520707,"alleles":["T","A","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1173138177","feature_type":"variation","strand":1,"end":140520708,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520708},{"seq_region_name":"7","id":"rs1396777248","clinical_significance":[],"strand":1,"feature_type":"variation","end":140520709,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520709,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1405913551","clinical_significance":[],"strand":1,"feature_type":"variation","end":140520712,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520712,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1795824824","seq_region_name":"7","alleles":["CC","C"],"end":140520713,"feature_type":"variation","strand":1,"source":"dbSNP","start":140520712,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520713,"feature_type":"variation","strand":1,"alleles":["-","AG"],"end":140520712,"clinical_significance":[],"seq_region_name":"7","id":"rs1432701533"},{"clinical_significance":[],"id":"rs1795825124","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520713,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140520713},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585538519","alleles":["A","G"],"end":140520714,"feature_type":"variation","strand":1,"source":"dbSNP","start":140520714,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520714,"source":"dbSNP","strand":1,"feature_type":"variation","end":140520715,"alleles":["AT","-"],"seq_region_name":"7","id":"rs1172768251","clinical_significance":[]},{"seq_region_name":"7","id":"rs528143241","clinical_significance":[],"start":140520715,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A","C"],"end":140520715,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520715,"feature_type":"variation","strand":1,"end":140520715,"alleles":["T","-"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795825518"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520717,"source":"dbSNP","strand":1,"feature_type":"variation","end":140520717,"alleles":["C","T"],"seq_region_name":"7","id":"rs1301826836","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795825779","end":140520717,"alleles":["-","GCCCGGCTTTTT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140520718,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520718,"feature_type":"variation","strand":1,"end":140520718,"alleles":["C","G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795825924"},{"seq_region_name":"7","id":"rs1400846299","clinical_significance":[],"start":140520719,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","T"],"end":140520719,"strand":1,"feature_type":"variation"},{"id":"rs1320492196","seq_region_name":"7","clinical_significance":[],"start":140520720,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140520720,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795826375","feature_type":"variation","strand":1,"end":140520722,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520722},{"clinical_significance":[],"seq_region_name":"7","id":"rs1324788285","alleles":["TAAT","T"],"end":140520726,"feature_type":"variation","strand":1,"source":"dbSNP","start":140520723,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1389401179","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520725,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140520725},{"clinical_significance":[],"seq_region_name":"7","id":"rs1430080780","source":"dbSNP","start":140520730,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["-","C"],"end":140520729,"feature_type":"variation","strand":1},{"end":140520730,"alleles":["-","CCAG"],"strand":1,"feature_type":"variation","start":140520731,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130447423","clinical_significance":[]},{"clinical_significance":[],"id":"rs1276006757","seq_region_name":"7","end":140520731,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140520731,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs2130447439","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520734,"source":"dbSNP","strand":1,"feature_type":"variation","end":140520733,"alleles":["-","GTTTTTTTTTTTCT"]},{"start":140520738,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140520738,"strand":1,"feature_type":"variation","id":"rs1455050012","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795826930","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140520743,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520743,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520748,"source":"dbSNP","strand":1,"feature_type":"variation","end":140520748,"alleles":["A","C","G"],"seq_region_name":"7","id":"rs1409250011","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795827226","end":140520754,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140520754,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140520755,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140520755,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1480623325"},{"end":140520756,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140520756,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs139930134","seq_region_name":"7","clinical_significance":[]},{"end":140520758,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140520758,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs149424532","seq_region_name":"7","clinical_significance":[]},{"end":140520760,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140520760,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795827828","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1450894661","feature_type":"variation","strand":1,"end":140520762,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520762},{"start":140520764,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140520764,"alleles":["G","T"],"strand":1,"feature_type":"variation","id":"rs532128232","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1032858004","end":140520765,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140520765,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs182525185","alleles":["G","A"],"end":140520773,"feature_type":"variation","strand":1,"source":"dbSNP","start":140520773,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1206548533","seq_region_name":"7","source":"dbSNP","start":140520776,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140520776,"feature_type":"variation","strand":1},{"id":"rs1327400760","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140520778,"strand":1,"feature_type":"variation","start":140520778,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140520778,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","-"],"end":140520778,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795828554","clinical_significance":[]},{"clinical_significance":[],"id":"rs1259203295","seq_region_name":"7","alleles":["G","A","C"],"end":140520779,"feature_type":"variation","strand":1,"source":"dbSNP","start":140520779,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["A","C","G"],"end":140520781,"feature_type":"variation","strand":1,"source":"dbSNP","start":140520781,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585538719"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520782,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140520782,"id":"rs1347767444","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520785,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140520785,"id":"rs1445956128","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1281714609","seq_region_name":"7","source":"dbSNP","start":140520787,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140520787,"alleles":["G","A"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520791,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140520791,"seq_region_name":"7","id":"rs1795829470","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs957408744","source":"dbSNP","start":140520796,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140520796,"alleles":["T","A","C"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140520801,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520801,"source":"dbSNP","seq_region_name":"7","id":"rs1198947958","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1010163232","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140520803,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520803},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140520805,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520805,"source":"dbSNP","seq_region_name":"7","id":"rs147544540","clinical_significance":[]},{"source":"dbSNP","start":140520806,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140520806,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1446693221"},{"seq_region_name":"7","id":"rs1795830357","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520808,"source":"dbSNP","strand":1,"feature_type":"variation","end":140520808,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1172865559","end":140520810,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140520810,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520811,"feature_type":"variation","strand":1,"end":140520811,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1386051490"},{"strand":1,"feature_type":"variation","end":140520812,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520812,"source":"dbSNP","seq_region_name":"7","id":"rs1795830795","clinical_significance":[]},{"start":140520817,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140520817,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs1380718832","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140520818,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520818,"clinical_significance":[],"seq_region_name":"7","id":"rs1455110668"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520819,"source":"dbSNP","strand":1,"feature_type":"variation","end":140520819,"alleles":["A","G"],"seq_region_name":"7","id":"rs1795831072","clinical_significance":[]},{"start":140520819,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AAA","AAAA"],"end":140520821,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs34483239","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140520822,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520822,"clinical_significance":[],"seq_region_name":"7","id":"rs1452196329"},{"seq_region_name":"7","id":"rs556514184","clinical_significance":[],"end":140520825,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140520825,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795831598","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520827,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140520827},{"alleles":["A","G"],"end":140520830,"strand":1,"feature_type":"variation","start":140520830,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130447731","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140520833,"alleles":["A","AA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520833,"clinical_significance":[],"id":"rs1795831695","seq_region_name":"7"},{"start":140520838,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140520838,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs140204268","clinical_significance":[]},{"source":"dbSNP","start":140520839,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140520839,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs12703977","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140520840,"alleles":["C","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520840,"clinical_significance":[],"seq_region_name":"7","id":"rs927392321"},{"id":"rs1400268172","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520840,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140520840},{"id":"rs1477668762","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520841,"source":"dbSNP","strand":1,"feature_type":"variation","end":140520841,"alleles":["G","A","C"]},{"seq_region_name":"7","id":"rs1324292494","clinical_significance":[],"end":140520842,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140520842,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs566638235","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140520843,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520843,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140520846,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520846,"source":"dbSNP","id":"rs1795832613","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140520848,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520848,"clinical_significance":[],"seq_region_name":"7","id":"rs1463594014"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795832701","end":140520850,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140520850,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140520851,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140520851,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs533995717"},{"start":140520852,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140520852,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795832890","clinical_significance":[]},{"seq_region_name":"7","id":"rs958832978","clinical_significance":[],"alleles":["C","T"],"end":140520854,"strand":1,"feature_type":"variation","start":140520854,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140520855,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520855,"source":"dbSNP","id":"rs1250247279","seq_region_name":"7","clinical_significance":[]},{"start":140520855,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["GG","G"],"end":140520856,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585538950","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140520857,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520857,"source":"dbSNP","seq_region_name":"7","id":"rs35407266","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs985259987","source":"dbSNP","start":140520861,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140520861,"feature_type":"variation","strand":1},{"alleles":["C","T"],"end":140520864,"strand":1,"feature_type":"variation","start":140520864,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1276991761","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs544954541","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140520865,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520865},{"strand":1,"feature_type":"variation","end":140520866,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520866,"source":"dbSNP","seq_region_name":"7","id":"rs1218960893","clinical_significance":[]},{"seq_region_name":"7","id":"rs1340746797","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520869,"source":"dbSNP","strand":1,"feature_type":"variation","end":140520869,"alleles":["A","G","T"]},{"seq_region_name":"7","id":"rs1795833814","clinical_significance":[],"end":140520870,"alleles":["-","A"],"strand":1,"feature_type":"variation","start":140520871,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs377256335","clinical_significance":[],"alleles":["TTTTTTTTTTT","TTTTTTTTTT","TTTTTTTTTTTT","TTTTTTTTTTTTT"],"end":140520881,"strand":1,"feature_type":"variation","start":140520871,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520880,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140520880,"seq_region_name":"7","id":"rs1795834106","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563113626","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520881,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140520881},{"source":"dbSNP","start":140520882,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","G","T"],"end":140520882,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs921603768"},{"start":140520883,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140520883,"strand":1,"feature_type":"variation","id":"rs1563113639","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1563113646","clinical_significance":[],"start":140520883,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TTTTTTT","TTTTTT","TTTTTTTT"],"end":140520889,"strand":1,"feature_type":"variation"},{"alleles":["T","A","C"],"end":140520889,"feature_type":"variation","strand":1,"source":"dbSNP","start":140520889,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795834696"},{"end":140520890,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140520890,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1439377473","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795834888","seq_region_name":"7","source":"dbSNP","start":140520891,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140520891,"alleles":["T","-"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs558913028","clinical_significance":[],"end":140520893,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140520893,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795835071","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140520894,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520894},{"source":"dbSNP","start":140520898,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140520898,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1378175687","seq_region_name":"7"},{"start":140520906,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140520906,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs2130448055","seq_region_name":"7","clinical_significance":[]},{"end":140520908,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140520908,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs35533954"},{"clinical_significance":[],"id":"rs1795835421","seq_region_name":"7","alleles":["TT","T"],"end":140520910,"feature_type":"variation","strand":1,"source":"dbSNP","start":140520909,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585539099","source":"dbSNP","start":140520913,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140520913,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795835641","clinical_significance":[],"start":140520914,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140520914,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1452955004","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520915,"feature_type":"variation","strand":1,"end":140520915,"alleles":["C","T"]},{"end":140520917,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140520917,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1407780219","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795837122","clinical_significance":[],"alleles":["G","C"],"end":140520920,"strand":1,"feature_type":"variation","start":140520920,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["C","A"],"end":140520921,"feature_type":"variation","strand":1,"source":"dbSNP","start":140520921,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585539131"},{"start":140520923,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140520923,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795837353","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520926,"source":"dbSNP","strand":1,"feature_type":"variation","end":140520940,"alleles":["GTGCAATGGTGCAAT","GTGCAAT"],"seq_region_name":"7","id":"rs1795837446","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520930,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140520930,"id":"rs577209975","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1332000342","clinical_significance":[],"alleles":["A","G"],"end":140520931,"strand":1,"feature_type":"variation","start":140520931,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520932,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140520932,"seq_region_name":"7","id":"rs1413665932","clinical_significance":[]},{"alleles":["G","A"],"end":140520936,"feature_type":"variation","strand":1,"source":"dbSNP","start":140520936,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1036605270"},{"strand":1,"feature_type":"variation","end":140520937,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520937,"source":"dbSNP","seq_region_name":"7","id":"rs923520780","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs187980279","alleles":["A","C","G"],"end":140520938,"feature_type":"variation","strand":1,"source":"dbSNP","start":140520938,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1050703612","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520939,"source":"dbSNP","strand":1,"feature_type":"variation","end":140520939,"alleles":["A","G"]},{"id":"rs1585539228","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140520940,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520940,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140520943,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520943,"clinical_significance":[],"id":"rs1462845334","seq_region_name":"7"},{"alleles":["G","A"],"end":140520944,"feature_type":"variation","strand":1,"source":"dbSNP","start":140520944,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1210003207"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520948,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140520948,"clinical_significance":[],"seq_region_name":"7","id":"rs139327049"},{"start":140520949,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140520949,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs149589424","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs191518042","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520952,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140520952},{"id":"rs1209908369","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520953,"source":"dbSNP","strand":1,"feature_type":"variation","end":140520953,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1192963246","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520956,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140520956},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520959,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140520959,"clinical_significance":[],"id":"rs1238678180","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs931594925","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520963,"feature_type":"variation","strand":1,"end":140520963,"alleles":["C","T"]},{"alleles":["T","C"],"end":140520967,"strand":1,"feature_type":"variation","start":140520967,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1275791133","seq_region_name":"7","clinical_significance":[]},{"id":"rs889421133","seq_region_name":"7","clinical_significance":[],"alleles":["G","T"],"end":140520969,"strand":1,"feature_type":"variation","start":140520969,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520973,"source":"dbSNP","strand":1,"feature_type":"variation","end":140520973,"alleles":["C","G"],"id":"rs1585539353","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140520976,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140520976,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795839524"},{"start":140520977,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140520977,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs916376501","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1420701940","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520978,"feature_type":"variation","strand":1,"end":140520978,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1179375099","feature_type":"variation","strand":1,"end":140520979,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520979},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520985,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140520985,"seq_region_name":"7","id":"rs1246039602","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140520989,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140520989,"source":"dbSNP","seq_region_name":"7","id":"rs1795839918","clinical_significance":[]},{"alleles":["T","C","G"],"end":140520994,"strand":1,"feature_type":"variation","start":140520994,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1054580705","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1165869891","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140520995,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140520995},{"seq_region_name":"7","id":"rs1447085068","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","-"],"end":140521002,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521002,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1354913775","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521004,"feature_type":"variation","strand":1,"end":140521004,"alleles":["A","C"]},{"strand":1,"feature_type":"variation","end":140521009,"alleles":["G","C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521009,"source":"dbSNP","seq_region_name":"7","id":"rs893003843","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521011,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140521011,"clinical_significance":[],"seq_region_name":"7","id":"rs969346243"},{"strand":1,"feature_type":"variation","end":140521015,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521015,"source":"dbSNP","seq_region_name":"7","id":"rs1396826479","clinical_significance":[]},{"start":140521018,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140521018,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795840760","clinical_significance":[]},{"source":"dbSNP","start":140521019,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140521019,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1164351846"},{"alleles":["G","A"],"end":140521020,"feature_type":"variation","strand":1,"source":"dbSNP","start":140521020,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs575158246"},{"source":"dbSNP","start":140521023,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140521023,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs909888298"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521025,"feature_type":"variation","strand":1,"end":140521025,"alleles":["C","A"],"clinical_significance":[],"id":"rs1411980832","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140521026,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521026,"source":"dbSNP","seq_region_name":"7","id":"rs1795841154","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521031,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140521031,"seq_region_name":"7","id":"rs1795841245","clinical_significance":[]},{"source":"dbSNP","start":140521032,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140521032,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795841345"},{"feature_type":"variation","strand":1,"end":140521033,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521033,"clinical_significance":[],"seq_region_name":"7","id":"rs2130448470"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140521041,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521041,"clinical_significance":[],"seq_region_name":"7","id":"rs1181483702"},{"source":"dbSNP","start":140521044,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140521044,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1470596674","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140521046,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521046,"source":"dbSNP","id":"rs542460527","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1020237741","clinical_significance":[],"strand":1,"feature_type":"variation","end":140521047,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521047,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1563113771","clinical_significance":[],"start":140521047,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TTTATTTT","TTT"],"end":140521054,"strand":1,"feature_type":"variation"},{"start":140521048,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140521048,"alleles":["T","A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1483042394","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795841986","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521049,"feature_type":"variation","strand":1,"end":140521049,"alleles":["T","C"]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140521050,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521050,"clinical_significance":[],"id":"rs1585539544","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140521060,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521060,"source":"dbSNP","id":"rs1037145581","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795842205","seq_region_name":"7","source":"dbSNP","start":140521064,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140521064,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521065,"source":"dbSNP","strand":1,"feature_type":"variation","end":140521065,"alleles":["A","G"],"seq_region_name":"7","id":"rs1293096990","clinical_significance":[]},{"source":"dbSNP","start":140521067,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140521067,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs918661719"},{"alleles":["G","T"],"end":140521068,"strand":1,"feature_type":"variation","start":140521068,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1222667745","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521069,"feature_type":"variation","strand":1,"end":140521069,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795842518"},{"source":"dbSNP","start":140521072,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140521072,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1322981058"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130448590","end":140521073,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140521073,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140521077,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140521077,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1325883900"},{"clinical_significance":[],"id":"rs1397821552","seq_region_name":"7","end":140521078,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140521078,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1795842918","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521080,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140521080},{"end":140521085,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140521085,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795843014"},{"seq_region_name":"7","id":"rs1795843102","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521085,"source":"dbSNP","strand":1,"feature_type":"variation","end":140521085,"alleles":["A","-"]},{"seq_region_name":"7","id":"rs1393568810","clinical_significance":[],"alleles":["G","A"],"end":140521087,"strand":1,"feature_type":"variation","start":140521087,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["T","C"],"end":140521088,"strand":1,"feature_type":"variation","start":140521088,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130448656","clinical_significance":[]},{"alleles":["T","G"],"end":140521089,"feature_type":"variation","strand":1,"source":"dbSNP","start":140521089,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795843297"},{"alleles":["G","A"],"end":140521090,"strand":1,"feature_type":"variation","start":140521090,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs934045893","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521091,"source":"dbSNP","strand":1,"feature_type":"variation","end":140521091,"alleles":["A","G","T"],"seq_region_name":"7","id":"rs1305315257","clinical_significance":[]},{"start":140521093,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140521093,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1335485077","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140521096,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521096,"source":"dbSNP","id":"rs1245095162","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140521098,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140521098,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795843846"},{"end":140521105,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140521105,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1051283713","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521107,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140521107,"seq_region_name":"7","id":"rs1459563976","clinical_significance":[]},{"seq_region_name":"7","id":"rs1348221240","clinical_significance":[],"strand":1,"feature_type":"variation","end":140521116,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521116,"source":"dbSNP"},{"end":140521117,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140521117,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs889916022"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1401525419","feature_type":"variation","strand":1,"end":140521118,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521118},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521119,"feature_type":"variation","strand":1,"end":140521119,"alleles":["G","A"],"clinical_significance":[],"id":"rs1007097202","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795844753","source":"dbSNP","start":140521120,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140521120,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1585539707","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521122,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140521122},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130448770","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140521127,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521127},{"start":140521128,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140521128,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1043955276","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs560629852","alleles":["C","T"],"end":140521130,"feature_type":"variation","strand":1,"source":"dbSNP","start":140521130,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521133,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140521133,"clinical_significance":[],"seq_region_name":"7","id":"rs1002764055"},{"strand":1,"feature_type":"variation","end":140521134,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521134,"source":"dbSNP","seq_region_name":"7","id":"rs903565115","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs554188476","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521135,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140521135},{"strand":1,"feature_type":"variation","end":140521136,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521136,"source":"dbSNP","seq_region_name":"7","id":"rs1031194444","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521139,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140521139,"seq_region_name":"7","id":"rs1795845806","clinical_significance":[]},{"start":140521139,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140521141,"alleles":["GTG","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1212493946","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130448841","clinical_significance":[],"end":140521142,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140521142,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs540002476","clinical_significance":[],"strand":1,"feature_type":"variation","end":140521144,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521144,"source":"dbSNP"},{"seq_region_name":"7","id":"rs960506987","clinical_significance":[],"alleles":["A","T"],"end":140521147,"strand":1,"feature_type":"variation","start":140521147,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140521151,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521151,"clinical_significance":[],"id":"rs1382458578","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521155,"feature_type":"variation","strand":1,"end":140521155,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs572343752"},{"clinical_significance":[],"id":"rs1023476485","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140521156,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521156},{"seq_region_name":"7","id":"rs1220127759","clinical_significance":[],"strand":1,"feature_type":"variation","end":140521161,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521161,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521162,"feature_type":"variation","strand":1,"end":140521162,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1481570426"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795847168","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521163,"feature_type":"variation","strand":1,"end":140521163,"alleles":["A","G"]},{"clinical_significance":[],"id":"rs1795847294","seq_region_name":"7","alleles":["C","T"],"end":140521164,"feature_type":"variation","strand":1,"source":"dbSNP","start":140521164,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","G","T"],"end":140521165,"feature_type":"variation","strand":1,"source":"dbSNP","start":140521165,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1193949749"},{"clinical_significance":[],"id":"rs984899296","seq_region_name":"7","alleles":["A","G"],"end":140521166,"feature_type":"variation","strand":1,"source":"dbSNP","start":140521166,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1442751109","clinical_significance":[],"end":140521169,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140521169,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1226422632","clinical_significance":[],"strand":1,"feature_type":"variation","end":140521171,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521171,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs375352785","end":140521172,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140521172,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795847889","end":140521173,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140521173,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1795847984","seq_region_name":"7","end":140521179,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140521179,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140521187,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140521187,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1016750743","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs111320478","alleles":["C","T"],"end":140521192,"feature_type":"variation","strand":1,"source":"dbSNP","start":140521192,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140521193,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521193,"clinical_significance":[],"seq_region_name":"7","id":"rs1795848287"},{"feature_type":"variation","strand":1,"end":140521195,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521195,"clinical_significance":[],"seq_region_name":"7","id":"rs768051552"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1365346655","end":140521203,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140521203,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521210,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140521210,"seq_region_name":"7","id":"rs1293064178","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521212,"source":"dbSNP","strand":1,"feature_type":"variation","end":140521212,"alleles":["C","T"],"seq_region_name":"7","id":"rs550137378","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140521216,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521216,"clinical_significance":[],"id":"rs542719210","seq_region_name":"7"},{"source":"dbSNP","start":140521221,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140521221,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795848819"},{"id":"rs2130449073","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521226,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140521226},{"seq_region_name":"7","id":"rs1795848918","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521236,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C","T"],"end":140521236},{"source":"dbSNP","start":140521238,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140521238,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs923553392"},{"clinical_significance":[],"id":"rs1795849081","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521240,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140521240},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521248,"source":"dbSNP","strand":1,"feature_type":"variation","end":140521248,"alleles":["A","C"],"seq_region_name":"7","id":"rs1585539967","clinical_significance":[]},{"seq_region_name":"7","id":"rs933586670","clinical_significance":[],"alleles":["C","T"],"end":140521249,"strand":1,"feature_type":"variation","start":140521249,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs986322070","end":140521252,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140521252,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","T"],"end":140521255,"feature_type":"variation","strand":1,"source":"dbSNP","start":140521255,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795849434"},{"clinical_significance":[],"id":"rs1178644022","seq_region_name":"7","feature_type":"variation","strand":1,"end":140521259,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521259},{"end":140521260,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140521260,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795849604","clinical_significance":[]},{"start":140521260,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140521265,"alleles":["CAATCA","CA"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1431973573","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795849780","source":"dbSNP","start":140521261,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140521261,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140521266,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521266,"clinical_significance":[],"seq_region_name":"7","id":"rs962727302"},{"seq_region_name":"7","id":"rs1795849949","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521268,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140521268},{"clinical_significance":[],"id":"rs1267250354","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521270,"feature_type":"variation","strand":1,"end":140521270,"alleles":["T","A"]},{"feature_type":"variation","strand":1,"end":140521276,"alleles":["TTTTT","TTTT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521272,"clinical_significance":[],"seq_region_name":"7","id":"rs1563113944"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521275,"source":"dbSNP","strand":1,"feature_type":"variation","end":140521275,"alleles":["T","A"],"id":"rs1795850225","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521282,"feature_type":"variation","strand":1,"alleles":["TTTTTTTTTT","TTTTTTTTT","TTTTTTTTTTT"],"end":140521291,"clinical_significance":[],"id":"rs910891661","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585540025","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521283,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140521283},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140521287,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521287,"source":"dbSNP","seq_region_name":"7","id":"rs562462246","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1373651326","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521292,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140521292},{"clinical_significance":[],"seq_region_name":"7","id":"rs1296904954","source":"dbSNP","start":140521294,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140521294,"feature_type":"variation","strand":1},{"start":140521294,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["GACGGAG","-"],"end":140521300,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1463990729","clinical_significance":[]},{"id":"rs918552266","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521296,"source":"dbSNP","strand":1,"feature_type":"variation","end":140521296,"alleles":["C","T"]},{"id":"rs775758331","seq_region_name":"7","clinical_significance":[],"end":140521297,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140521297,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs934096059","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521304,"feature_type":"variation","strand":1,"end":140521304,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795852357","feature_type":"variation","strand":1,"alleles":["AA","A"],"end":140521314,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521313},{"strand":1,"feature_type":"variation","end":140521314,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521314,"source":"dbSNP","id":"rs1300495962","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1353162468","clinical_significance":[],"start":140521315,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G","T"],"end":140521315,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140521316,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521316,"clinical_significance":[],"seq_region_name":"7","id":"rs1795852810"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1232217754","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521319,"feature_type":"variation","strand":1,"end":140521319,"alleles":["G","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1367452925","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521320,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140521320},{"source":"dbSNP","start":140521325,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140521325,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1318544287"},{"clinical_significance":[],"id":"rs1051576148","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521326,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140521326},{"start":140521329,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140521329,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795853543","clinical_significance":[]},{"source":"dbSNP","start":140521331,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140521331,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs529903312"},{"end":140521335,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140521335,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795853817"},{"seq_region_name":"7","id":"rs1795853950","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140521337,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521337,"source":"dbSNP"},{"alleles":["A","C"],"end":140521338,"strand":1,"feature_type":"variation","start":140521338,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795854094","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521340,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140521340,"id":"rs547989257","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140521341,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140521341,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs942866042","seq_region_name":"7"},{"seq_region_name":"7","id":"rs147773056","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140521342,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521342,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1308701316","clinical_significance":[],"start":140521343,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140521343,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs111418008","feature_type":"variation","strand":1,"end":140521344,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521344},{"clinical_significance":[],"seq_region_name":"7","id":"rs1451818458","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140521345,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521345},{"clinical_significance":[],"id":"rs182554091","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140521359,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521359},{"strand":1,"feature_type":"variation","end":140521363,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521363,"source":"dbSNP","id":"rs372695110","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795855011","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521364,"feature_type":"variation","strand":1,"end":140521364,"alleles":["C","T"]},{"start":140521368,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140521368,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795855105","clinical_significance":[]},{"seq_region_name":"7","id":"rs1052119997","clinical_significance":[],"start":140521369,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140521369,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1795855317","clinical_significance":[],"end":140521370,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140521370,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1464197892","clinical_significance":[],"strand":1,"feature_type":"variation","end":140521371,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521371,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795855507","clinical_significance":[],"start":140521378,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140521378,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1795855594","seq_region_name":"7","alleles":["C","T"],"end":140521383,"feature_type":"variation","strand":1,"source":"dbSNP","start":140521383,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1243340897","seq_region_name":"7","clinical_significance":[],"start":140521384,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140521384,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521392,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140521392,"seq_region_name":"7","id":"rs1795855797","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs896106436","alleles":["T","C"],"end":140521393,"feature_type":"variation","strand":1,"source":"dbSNP","start":140521393,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","T"],"end":140521396,"strand":1,"feature_type":"variation","start":140521396,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1034644176","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1482144262","source":"dbSNP","start":140521397,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140521397,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795856192","alleles":["G","A"],"end":140521401,"feature_type":"variation","strand":1,"source":"dbSNP","start":140521401,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521411,"source":"dbSNP","strand":1,"feature_type":"variation","end":140521412,"alleles":["CC","C"],"seq_region_name":"7","id":"rs1255135464","clinical_significance":[]},{"source":"dbSNP","start":140521412,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140521412,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs894508675","seq_region_name":"7"},{"start":140521414,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140521414,"strand":1,"feature_type":"variation","id":"rs1795856520","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140521420,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521420,"clinical_significance":[],"seq_region_name":"7","id":"rs1344171116"},{"id":"rs1484816691","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140521426,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521426,"source":"dbSNP"},{"id":"rs1795856802","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140521428,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521428,"source":"dbSNP"},{"start":140521430,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140521430,"strand":1,"feature_type":"variation","id":"rs1295530627","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130449654","clinical_significance":[],"alleles":["A","G"],"end":140521431,"strand":1,"feature_type":"variation","start":140521431,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1013340452","source":"dbSNP","start":140521432,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140521432,"alleles":["C","T"],"feature_type":"variation","strand":1},{"alleles":["C","A","T"],"end":140521433,"feature_type":"variation","strand":1,"source":"dbSNP","start":140521433,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1187420244","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521434,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140521434,"clinical_significance":[],"seq_region_name":"7","id":"rs1023803323"},{"source":"dbSNP","start":140521436,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140521436,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795857295"},{"seq_region_name":"7","id":"rs1016371846","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140521437,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521437,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795857383","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521440,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140521440},{"strand":1,"feature_type":"variation","end":140521446,"alleles":["T","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521446,"source":"dbSNP","seq_region_name":"7","id":"rs969238081","clinical_significance":[]},{"seq_region_name":"7","id":"rs1006039385","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521453,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140521453},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140521461,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521461,"clinical_significance":[],"seq_region_name":"7","id":"rs1432205965"},{"alleles":["G","A"],"end":140521468,"feature_type":"variation","strand":1,"source":"dbSNP","start":140521468,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1369221583"},{"seq_region_name":"7","id":"rs1169003074","clinical_significance":[],"end":140521471,"alleles":["TT","TTT"],"strand":1,"feature_type":"variation","start":140521470,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1372983439","clinical_significance":[],"start":140521472,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140521472,"alleles":["G","GG"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1795858100","seq_region_name":"7","source":"dbSNP","start":140521473,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140521473,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1563114074","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521474,"feature_type":"variation","strand":1,"end":140521474,"alleles":["A","C"]},{"start":140521477,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140521477,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795858287","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140521478,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521478,"source":"dbSNP","seq_region_name":"7","id":"rs1795858384","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521479,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140521479,"clinical_significance":[],"seq_region_name":"7","id":"rs962088575"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795858580","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521483,"feature_type":"variation","strand":1,"end":140521483,"alleles":["T","C"]},{"strand":1,"feature_type":"variation","end":140521492,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521492,"source":"dbSNP","seq_region_name":"7","id":"rs570903634","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585540418","clinical_significance":[],"strand":1,"feature_type":"variation","end":140521493,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521493,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521495,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140521495,"seq_region_name":"7","id":"rs1795858850","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795858939","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140521496,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521496},{"alleles":["T","C"],"end":140521504,"feature_type":"variation","strand":1,"source":"dbSNP","start":140521504,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795859031","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521506,"feature_type":"variation","strand":1,"end":140521506,"alleles":["A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795859172"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521507,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140521507,"clinical_significance":[],"seq_region_name":"7","id":"rs535750050"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521511,"feature_type":"variation","strand":1,"end":140521511,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs972092205"},{"seq_region_name":"7","id":"rs187182916","clinical_significance":[],"start":140521512,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C","G"],"end":140521512,"strand":1,"feature_type":"variation"},{"start":140521515,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140521515,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795859845","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1030474836","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521517,"feature_type":"variation","strand":1,"end":140521517,"alleles":["T","C"]},{"clinical_significance":[],"id":"rs1795860161","seq_region_name":"7","feature_type":"variation","strand":1,"end":140521520,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521520},{"feature_type":"variation","strand":1,"end":140521530,"alleles":["GCATGCCTTGG","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521520,"clinical_significance":[],"seq_region_name":"7","id":"rs1189202906"},{"id":"rs1795860441","seq_region_name":"7","clinical_significance":[],"alleles":["C","A"],"end":140521521,"strand":1,"feature_type":"variation","start":140521521,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795860606","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521522,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140521522},{"source":"dbSNP","start":140521523,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C","G"],"end":140521523,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1421617703"},{"start":140521524,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140521524,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs1795860912","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","G","T"],"end":140521525,"feature_type":"variation","strand":1,"source":"dbSNP","start":140521525,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1016080526"},{"seq_region_name":"7","id":"rs1795861134","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521528,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140521528},{"id":"rs954836683","seq_region_name":"7","clinical_significance":[],"alleles":["G","-"],"end":140521540,"strand":1,"feature_type":"variation","start":140521540,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795861336","source":"dbSNP","start":140521545,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140521545,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795861439","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140521546,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521546,"source":"dbSNP"},{"source":"dbSNP","start":140521553,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140521555,"alleles":["AGG","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795861544","seq_region_name":"7"},{"source":"dbSNP","start":140521556,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140521556,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1272352995"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521557,"feature_type":"variation","strand":1,"end":140521557,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1435788965"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521559,"source":"dbSNP","strand":1,"feature_type":"variation","end":140521559,"alleles":["G","C"],"seq_region_name":"7","id":"rs986380759","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795861904","clinical_significance":[],"end":140521560,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140521560,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1795862006","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140521562,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521562,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521566,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140521566,"clinical_significance":[],"seq_region_name":"7","id":"rs1795862088"},{"clinical_significance":[],"id":"rs1795862187","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521567,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140521567},{"seq_region_name":"7","id":"rs1795862274","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140521569,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521569,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130450073","feature_type":"variation","strand":1,"alleles":["T","-"],"end":140521570,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521570},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521571,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140521571,"seq_region_name":"7","id":"rs1175908115","clinical_significance":[]},{"end":140521574,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140521574,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130450091"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795862466","source":"dbSNP","start":140521579,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140521579,"alleles":["C","T"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140521580,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140521580,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795862576"},{"id":"rs1795862662","seq_region_name":"7","clinical_significance":[],"start":140521589,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140521589,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1267242162","source":"dbSNP","start":140521590,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140521590,"feature_type":"variation","strand":1},{"id":"rs1795862848","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140521592,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521592,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795862952","clinical_significance":[],"strand":1,"feature_type":"variation","end":140521596,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521596,"source":"dbSNP"},{"seq_region_name":"7","id":"rs910792698","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521600,"source":"dbSNP","strand":1,"feature_type":"variation","end":140521600,"alleles":["G","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521611,"source":"dbSNP","strand":1,"feature_type":"variation","end":140521611,"alleles":["A","G"],"id":"rs1795863130","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs556565283","seq_region_name":"7","alleles":["T","G"],"end":140521612,"feature_type":"variation","strand":1,"source":"dbSNP","start":140521612,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140521618,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140521618,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130450175","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140521621,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521621,"source":"dbSNP","seq_region_name":"7","id":"rs979197091","clinical_significance":[]},{"seq_region_name":"7","id":"rs942405301","clinical_significance":[],"start":140521623,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140521623,"alleles":["C","G","T"],"strand":1,"feature_type":"variation"},{"alleles":["G","A"],"end":140521632,"feature_type":"variation","strand":1,"source":"dbSNP","start":140521632,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795863594"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1349252112","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140521636,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521636},{"seq_region_name":"7","id":"rs2130450216","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140521637,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521637,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs113602766","source":"dbSNP","start":140521641,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140521641,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795863902","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521643,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140521643},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140521645,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521645,"source":"dbSNP","seq_region_name":"7","id":"rs1425779237","clinical_significance":[]},{"clinical_significance":[],"id":"rs1025643777","seq_region_name":"7","feature_type":"variation","strand":1,"end":140521646,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521646},{"end":140521651,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140521651,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1380007354"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795864257","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140521655,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521655},{"clinical_significance":[],"seq_region_name":"7","id":"rs955552731","end":140521658,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140521658,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795864489","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521662,"source":"dbSNP","strand":1,"feature_type":"variation","end":140521662,"alleles":["G","T"]},{"start":140521668,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140521668,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs986936976","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1367511783","seq_region_name":"7","source":"dbSNP","start":140521669,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140521669,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1585540684","clinical_significance":[],"strand":1,"feature_type":"variation","end":140521670,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521670,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs568780930","source":"dbSNP","start":140521671,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140521671,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795864960","end":140521672,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140521672,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795865042","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521679,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140521679},{"seq_region_name":"7","id":"rs1473449325","clinical_significance":[],"end":140521680,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140521680,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs560997432","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521680,"feature_type":"variation","strand":1,"alleles":["CC","C"],"end":140521681},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521683,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140521683,"clinical_significance":[],"seq_region_name":"7","id":"rs1795865320"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1249605017","end":140521687,"alleles":["A","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140521687,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521688,"feature_type":"variation","strand":1,"alleles":["GGGGG","GGGGGGG"],"end":140521692,"clinical_significance":[],"seq_region_name":"7","id":"rs1181385626"},{"end":140521692,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140521692,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130450386"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1452046509","end":140521697,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140521697,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs2130450403","clinical_significance":[],"start":140521699,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140521699,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140521700,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521700,"clinical_significance":[],"seq_region_name":"7","id":"rs1795865717"},{"seq_region_name":"7","id":"rs1269599033","clinical_significance":[],"strand":1,"feature_type":"variation","end":140521703,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521703,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1795866112","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521704,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140521704},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795866189","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521708,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140521708},{"seq_region_name":"7","id":"rs1795866285","clinical_significance":[],"strand":1,"feature_type":"variation","end":140521717,"alleles":["CAGGGCA","CA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521711,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs536112846","source":"dbSNP","start":140521713,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140521713,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs554505794","clinical_significance":[],"end":140521714,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140521714,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140521725,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521725,"clinical_significance":[],"seq_region_name":"7","id":"rs1355959378"},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140521727,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521727,"source":"dbSNP","seq_region_name":"7","id":"rs1269002679","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795866792","clinical_significance":[],"start":140521734,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["GGGGG","GGGG"],"end":140521738,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1795866892","seq_region_name":"7","end":140521735,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140521735,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1585540791","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521738,"source":"dbSNP","strand":1,"feature_type":"variation","end":140521738,"alleles":["G","A"]},{"strand":1,"feature_type":"variation","end":140521741,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521741,"source":"dbSNP","seq_region_name":"7","id":"rs2130450526","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521745,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140521745,"seq_region_name":"7","id":"rs1230685877","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130450543","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521746,"feature_type":"variation","strand":1,"end":140521746,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs764403925","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140521751,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521751,"source":"dbSNP"},{"alleles":["C","T"],"end":140521753,"feature_type":"variation","strand":1,"source":"dbSNP","start":140521753,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1288042423"},{"id":"rs1277942127","seq_region_name":"7","clinical_significance":[],"end":140521755,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140521755,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1795867363","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["TGTG","TG"],"end":140521761,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521758,"source":"dbSNP"},{"source":"dbSNP","start":140521762,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140521762,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795867447"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795867531","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521764,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140521764},{"seq_region_name":"7","id":"rs1795867618","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521770,"source":"dbSNP","strand":1,"feature_type":"variation","end":140521770,"alleles":["C","G"]},{"strand":1,"feature_type":"variation","end":140521771,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521771,"source":"dbSNP","id":"rs1795867688","seq_region_name":"7","clinical_significance":[]},{"start":140521772,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140521772,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795867781","clinical_significance":[]},{"seq_region_name":"7","id":"rs1406124627","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521777,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140521777},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521778,"feature_type":"variation","strand":1,"end":140521778,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs780276677"},{"id":"rs1795868065","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521781,"source":"dbSNP","strand":1,"feature_type":"variation","end":140521781,"alleles":["C","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521783,"feature_type":"variation","strand":1,"end":140521783,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795868169"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521785,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140521785,"clinical_significance":[],"seq_region_name":"7","id":"rs1795868248"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521787,"feature_type":"variation","strand":1,"end":140521787,"alleles":["A","C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs925426138"},{"clinical_significance":[],"id":"rs1795868477","seq_region_name":"7","source":"dbSNP","start":140521790,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140521790,"alleles":["C","T"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140521791,"alleles":["A","C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521791,"source":"dbSNP","seq_region_name":"7","id":"rs753809805","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795868675","seq_region_name":"7","feature_type":"variation","strand":1,"end":140521796,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521796},{"start":140521797,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140521797,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1261498994","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140521798,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521798,"clinical_significance":[],"seq_region_name":"7","id":"rs112781685"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1053077452","feature_type":"variation","strand":1,"end":140521799,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521799},{"source":"dbSNP","start":140521801,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140521801,"alleles":["T","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795869087"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521804,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140521804,"id":"rs760900343","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs766522127","end":140521806,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140521806,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521807,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140521807,"id":"rs938485071","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140521808,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521808,"clinical_significance":[],"seq_region_name":"7","id":"rs1795869477"},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140521813,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521813,"source":"dbSNP","seq_region_name":"7","id":"rs370582001","clinical_significance":[]},{"seq_region_name":"7","id":"rs1409493784","clinical_significance":[],"start":140521814,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140521814,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs753887128","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140521817,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521817,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140521818,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521818,"clinical_significance":[],"id":"rs1795869798","seq_region_name":"7"},{"alleles":["C","T"],"end":140521821,"feature_type":"variation","strand":1,"source":"dbSNP","start":140521821,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs2130450801","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140521825,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521825,"clinical_significance":[],"seq_region_name":"7","id":"rs1322801864"},{"start":140521827,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G","T"],"end":140521827,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs755007816","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140521828,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140521828,"source":"dbSNP","id":"rs751522016","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795870242","clinical_significance":[],"end":140521835,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140521835,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140521836,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140521836,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs757300615"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795870474","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521842,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140521842},{"seq_region_name":"7","id":"rs1585541047","clinical_significance":[],"alleles":["G","C"],"end":140521846,"strand":1,"feature_type":"variation","start":140521846,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"splice_region_variant","start":140521848,"source":"dbSNP","strand":1,"feature_type":"variation","end":140521848,"alleles":["C","G"],"seq_region_name":"7","id":"rs781096739","clinical_significance":[]},{"seq_region_name":"7","id":"rs949058712","clinical_significance":[],"strand":1,"feature_type":"variation","end":140521849,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"splice_donor_region_variant","start":140521849,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1585541085","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140521853,"assembly_name":"GRCh38","consequence_type":"splice_donor_variant","start":140521853,"source":"dbSNP"},{"end":140521854,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140521854,"consequence_type":"splice_donor_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs745673798"},{"seq_region_name":"7","id":"rs1309285548","clinical_significance":[],"end":140521859,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140521859,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant"},{"start":140521860,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140521860,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs1334178787","seq_region_name":"7","clinical_significance":[]},{"id":"rs1238669126","seq_region_name":"7","clinical_significance":[],"alleles":["A","G"],"end":140521862,"strand":1,"feature_type":"variation","start":140521862,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant"},{"clinical_significance":["uncertain significance"],"seq_region_name":"7","id":"rs1266393139","alleles":["T","A","C"],"end":140521863,"feature_type":"variation","strand":1,"source":"dbSNP","start":140521863,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"id":"rs1337316941","seq_region_name":"7","clinical_significance":[],"start":140521864,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140521864,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs757340192","feature_type":"variation","strand":1,"end":140521866,"alleles":["T","G"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521866},{"id":"rs1212220136","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140521868,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140521868,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140521869,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140521869,"seq_region_name":"7","id":"rs202110826","clinical_significance":["uncertain significance"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1005946106","source":"dbSNP","start":140521870,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140521870,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140521870,"consequence_type":"frameshift_variant","assembly_name":"GRCh38","end":140521871,"alleles":["GG","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1563114302"},{"end":140521872,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140521872,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","id":"rs779580171","seq_region_name":"7","clinical_significance":["uncertain significance"]},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521873,"feature_type":"variation","strand":1,"end":140521873,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs558395690"},{"end":140521877,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140521877,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","seq_region_name":"7","id":"rs768145024","clinical_significance":[]},{"alleles":["C","T"],"end":140521879,"strand":1,"feature_type":"variation","start":140521879,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs773888010","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs762264653","source":"dbSNP","start":140521880,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140521880,"feature_type":"variation","strand":1},{"id":"rs368814564","seq_region_name":"7","clinical_significance":["uncertain significance"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140521881,"source":"dbSNP","strand":1,"feature_type":"variation","end":140521881,"alleles":["C","T"]},{"end":140521882,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140521882,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs372102093","clinical_significance":[]},{"alleles":["C","G"],"end":140521885,"strand":1,"feature_type":"variation","start":140521885,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","id":"rs1795872637","seq_region_name":"7","clinical_significance":[]},{"end":140521887,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140521887,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs576841801","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140521889,"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140521889,"source":"dbSNP","seq_region_name":"7","id":"rs531807720","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs897621525","end":140521891,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140521891,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1466117122","seq_region_name":"7","consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521895,"feature_type":"variation","strand":1,"end":140521895,"alleles":["G","A"]},{"id":"rs766831304","seq_region_name":"7","clinical_significance":[],"start":140521896,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140521896,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs148419180","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521899,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140521899},{"start":140521900,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["G","A"],"end":140521900,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs759886035","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795873542","clinical_significance":[],"start":140521908,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["T","C"],"end":140521908,"strand":1,"feature_type":"variation"},{"end":140521911,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140521911,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs1228294239","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs368264444","feature_type":"variation","strand":1,"end":140521913,"alleles":["C","T"],"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521913},{"id":"rs752856607","seq_region_name":"7","clinical_significance":[],"start":140521917,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["A","G"],"end":140521917,"strand":1,"feature_type":"variation"},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521918,"feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140521918,"clinical_significance":[],"seq_region_name":"7","id":"rs757214468"},{"clinical_significance":[],"id":"rs1330020425","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140521922,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521922},{"seq_region_name":"7","id":"rs1795874202","clinical_significance":["uncertain significance"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140521924,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140521924},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140521925,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521925,"clinical_significance":["uncertain significance"],"seq_region_name":"7","id":"rs781007205"},{"clinical_significance":[],"id":"rs2130451234","seq_region_name":"7","alleles":["C","T"],"end":140521928,"feature_type":"variation","strand":1,"source":"dbSNP","start":140521928,"consequence_type":"synonymous_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140521931,"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140521931,"source":"dbSNP","seq_region_name":"7","id":"rs562102502","clinical_significance":[]},{"seq_region_name":"7","id":"rs750168986","clinical_significance":[],"start":140521934,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","end":140521934,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"end":140521937,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140521937,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs755859873","seq_region_name":"7"},{"seq_region_name":"7","id":"rs779960525","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140521938,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140521938},{"strand":1,"feature_type":"variation","end":140521939,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140521939,"source":"dbSNP","seq_region_name":"7","id":"rs1479333982","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1436871288","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140521943,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521943},{"alleles":["T","C"],"end":140521948,"feature_type":"variation","strand":1,"source":"dbSNP","start":140521948,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1385929005"},{"start":140521949,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","end":140521949,"alleles":["G","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs993545668","clinical_significance":[]},{"id":"rs1795875183","seq_region_name":"7","clinical_significance":[],"start":140521952,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","alleles":["G","A"],"end":140521952,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs955431796","clinical_significance":[],"end":140521953,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140521953,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"clinical_significance":[],"id":"rs1194749291","seq_region_name":"7","alleles":["G","A"],"end":140521955,"feature_type":"variation","strand":1,"source":"dbSNP","start":140521955,"consequence_type":"synonymous_variant","assembly_name":"GRCh38"},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521957,"feature_type":"variation","strand":1,"end":140521957,"alleles":["C","T"],"clinical_significance":["uncertain significance"],"id":"rs372133526","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795875567","end":140521964,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140521964,"consequence_type":"synonymous_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs376717563","end":140521965,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140521965,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1185495323","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521966,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140521966},{"clinical_significance":[],"seq_region_name":"7","id":"rs192139201","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521977,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140521977},{"seq_region_name":"7","id":"rs747667851","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140521978,"source":"dbSNP","strand":1,"feature_type":"variation","end":140521978,"alleles":["G","A","C"]},{"seq_region_name":"7","id":"rs772500499","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140521982,"source":"dbSNP","strand":1,"feature_type":"variation","end":140521982,"alleles":["C","T"]},{"clinical_significance":[],"id":"rs61737087","seq_region_name":"7","source":"dbSNP","start":140521984,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140521984,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs201125871","clinical_significance":["uncertain significance"],"start":140521987,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140521987,"alleles":["T","A","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs200491602","feature_type":"variation","strand":1,"end":140521990,"alleles":["T","A"],"consequence_type":"stop_gained","assembly_name":"GRCh38","source":"dbSNP","start":140521990},{"seq_region_name":"7","id":"rs1795876627","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"inframe_deletion","start":140521991,"source":"dbSNP","strand":1,"feature_type":"variation","end":140521996,"alleles":["CTCCTC","CTC"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795876717","consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140521994,"feature_type":"variation","strand":1,"end":140521994,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs777094305","clinical_significance":[],"start":140521995,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["T","A"],"end":140521995,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1795876896","clinical_significance":[],"alleles":["A","G","T"],"end":140521997,"strand":1,"feature_type":"variation","start":140521997,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs751559195","alleles":["C","T"],"end":140521998,"feature_type":"variation","strand":1,"source":"dbSNP","start":140521998,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs759792604","source":"dbSNP","start":140521999,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140521999,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795877379","consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522000,"feature_type":"variation","strand":1,"end":140522000,"alleles":["C","T"]},{"clinical_significance":["uncertain significance"],"seq_region_name":"7","id":"rs765581146","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522002,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140522002},{"clinical_significance":[],"seq_region_name":"7","id":"rs775655015","alleles":["G","A","T"],"end":140522003,"feature_type":"variation","strand":1,"source":"dbSNP","start":140522003,"consequence_type":"synonymous_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs764303784","seq_region_name":"7","consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522006,"feature_type":"variation","strand":1,"end":140522006,"alleles":["C","T"]},{"end":140522007,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140522007,"consequence_type":"stop_gained","assembly_name":"GRCh38","clinical_significance":["uncertain significance"],"seq_region_name":"7","id":"rs371591723"},{"seq_region_name":"7","id":"rs756130122","clinical_significance":[],"start":140522009,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","end":140522009,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":["uncertain significance"],"seq_region_name":"7","id":"rs202112514","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522010,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140522010},{"source":"dbSNP","start":140522017,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140522017,"feature_type":"variation","strand":1,"clinical_significance":["uncertain significance"],"seq_region_name":"7","id":"rs753651444"},{"end":140522018,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140522018,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","seq_region_name":"7","id":"rs754564650","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795878806","consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522020,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140522020},{"alleles":["A","G"],"end":140522023,"feature_type":"variation","strand":1,"source":"dbSNP","start":140522023,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs778538204"},{"clinical_significance":[],"id":"rs925457225","seq_region_name":"7","alleles":["G","T"],"end":140522029,"feature_type":"variation","strand":1,"source":"dbSNP","start":140522029,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs747862380","clinical_significance":[],"end":140522032,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140522032,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"seq_region_name":"7","id":"rs370020995","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140522033,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140522033},{"clinical_significance":[],"seq_region_name":"7","id":"rs757832276","source":"dbSNP","start":140522036,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140522036,"alleles":["A","C"],"feature_type":"variation","strand":1},{"id":"rs185448935","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140522037,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140522037,"source":"dbSNP"},{"alleles":["C","G","T"],"end":140522039,"feature_type":"variation","strand":1,"source":"dbSNP","start":140522039,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs747441467"},{"alleles":["T","C"],"end":140522040,"feature_type":"variation","strand":1,"source":"dbSNP","start":140522040,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs771501270"},{"seq_region_name":"7","id":"rs918143759","clinical_significance":[],"start":140522041,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140522041,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140522044,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140522044,"feature_type":"variation","strand":1,"clinical_significance":["uncertain significance"],"seq_region_name":"7","id":"rs776812553"},{"seq_region_name":"7","id":"rs377365858","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140522045,"source":"dbSNP","strand":1,"feature_type":"variation","end":140522045,"alleles":["G","A","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs775853504","source":"dbSNP","start":140522052,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140522052,"alleles":["C","T"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140522053,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522053,"clinical_significance":[],"id":"rs763327681","seq_region_name":"7"},{"end":140522056,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140522056,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs201538505","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795880784","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140522059,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522059},{"clinical_significance":[],"seq_region_name":"7","id":"rs774533553","source":"dbSNP","start":140522060,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","end":140522060,"alleles":["G","A"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["G","C","T"],"end":140522061,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140522061,"source":"dbSNP","seq_region_name":"7","id":"rs749296380","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130451770","clinical_significance":[],"end":140522063,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140522063,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant"},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140522065,"source":"dbSNP","strand":1,"feature_type":"variation","end":140522065,"alleles":["C","T"],"id":"rs1361833470","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140522066,"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140522066,"source":"dbSNP","seq_region_name":"7","id":"rs1795881223","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140522068,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140522068,"source":"dbSNP","id":"rs766348939","seq_region_name":"7","clinical_significance":[]},{"end":140522070,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140522070,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1473862366"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140522075,"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140522075,"source":"dbSNP","seq_region_name":"7","id":"rs1387913257","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140522077,"alleles":["C","T"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522077,"clinical_significance":[],"seq_region_name":"7","id":"rs780892963"},{"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140522078,"source":"dbSNP","strand":1,"feature_type":"variation","end":140522078,"alleles":["G","A"],"seq_region_name":"7","id":"rs61737088","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140522086,"source":"dbSNP","strand":1,"feature_type":"variation","end":140522086,"alleles":["G","C"],"seq_region_name":"7","id":"rs1231449553","clinical_significance":[]},{"alleles":["G","T"],"end":140522087,"strand":1,"feature_type":"variation","start":140522087,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs1795881909","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140522089,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140522089,"seq_region_name":"7","id":"rs765072383","clinical_significance":[]},{"id":"rs752324657","seq_region_name":"7","clinical_significance":["uncertain significance"],"start":140522091,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["G","T"],"end":140522091,"strand":1,"feature_type":"variation"},{"start":140522096,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","end":140522096,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1217636787","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1240189082","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140522097,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522097},{"clinical_significance":[],"seq_region_name":"7","id":"rs1277359671","alleles":["C","T"],"end":140522100,"feature_type":"variation","strand":1,"source":"dbSNP","start":140522100,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"start":140522102,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_acceptor_variant","alleles":["T","G"],"end":140522102,"strand":1,"feature_type":"variation","id":"rs1795882476","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140522109,"alleles":["GAGTAAG","G"],"assembly_name":"GRCh38","consequence_type":"splice_region_variant","start":140522103,"source":"dbSNP","seq_region_name":"7","id":"rs1795882530","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs758108878","end":140522106,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140522106,"consequence_type":"splice_region_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1206752169","consequence_type":"splice_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522107,"feature_type":"variation","strand":1,"end":140522107,"alleles":["A","G"]},{"start":140522108,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_region_variant","end":140522108,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","id":"rs941959514","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs777107630","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"splice_polypyrimidine_tract_variant","start":140522109,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140522109},{"clinical_significance":[],"seq_region_name":"7","id":"rs1194257474","source":"dbSNP","start":140522114,"consequence_type":"splice_polypyrimidine_tract_variant","assembly_name":"GRCh38","end":140522114,"alleles":["G","A"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522119,"source":"dbSNP","strand":1,"feature_type":"variation","end":140522119,"alleles":["G","A"],"seq_region_name":"7","id":"rs1037583744","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522120,"feature_type":"variation","strand":1,"end":140522120,"alleles":["G","A","C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs190320727"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522125,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140522125,"seq_region_name":"7","id":"rs781766044","clinical_significance":[]},{"end":140522128,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140522128,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs746446543","clinical_significance":[]},{"end":140522129,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140522129,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs201876576"},{"feature_type":"variation","strand":1,"end":140522134,"alleles":["G","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522134,"clinical_significance":[],"id":"rs1795883644","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140522135,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522135,"clinical_significance":[],"seq_region_name":"7","id":"rs866737321"},{"end":140522138,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140522138,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1408938962"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1402702703","end":140522139,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140522139,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522148,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140522148,"clinical_significance":[],"seq_region_name":"7","id":"rs1795883998"},{"id":"rs7786835","seq_region_name":"7","clinical_significance":[],"start":140522149,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140522149,"strand":1,"feature_type":"variation"},{"start":140522152,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140522152,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1345031750","clinical_significance":[]},{"start":140522153,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140522153,"strand":1,"feature_type":"variation","id":"rs1795884263","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs993722439","seq_region_name":"7","source":"dbSNP","start":140522155,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140522155,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140522158,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522158,"source":"dbSNP","seq_region_name":"7","id":"rs890528096","clinical_significance":[]},{"end":140522163,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140522163,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795884541"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522164,"feature_type":"variation","strand":1,"end":140522164,"alleles":["A","T"],"clinical_significance":[],"id":"rs1795884625","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522167,"feature_type":"variation","strand":1,"end":140522167,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs781606448"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795884840","feature_type":"variation","strand":1,"end":140522169,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522169},{"clinical_significance":[],"id":"rs1323862351","seq_region_name":"7","source":"dbSNP","start":140522172,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140522172,"feature_type":"variation","strand":1},{"alleles":["T","C"],"end":140522173,"strand":1,"feature_type":"variation","start":140522173,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs142586390","clinical_significance":[]},{"source":"dbSNP","start":140522175,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140522175,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1442737584"},{"id":"rs1795885234","seq_region_name":"7","clinical_significance":[],"alleles":["A","G"],"end":140522183,"strand":1,"feature_type":"variation","start":140522183,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140522184,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","start":140522184,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1163083061","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1281073418","end":140522196,"alleles":["GAACAGTAACTG","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140522185,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140522188,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140522188,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795885502"},{"source":"dbSNP","start":140522189,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140522189,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs745571764","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1007450798","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522194,"feature_type":"variation","strand":1,"end":140522194,"alleles":["C","G","T"]},{"clinical_significance":[],"id":"rs1180653898","seq_region_name":"7","alleles":["C","T"],"end":140522197,"feature_type":"variation","strand":1,"source":"dbSNP","start":140522197,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs777495879","source":"dbSNP","start":140522200,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140522200,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs556760186","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522206,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140522206},{"feature_type":"variation","strand":1,"end":140522208,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522208,"clinical_significance":[],"seq_region_name":"7","id":"rs2130452203"},{"start":140522209,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140522209,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs963975258","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140522210,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522210,"source":"dbSNP","id":"rs1370829916","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","A"],"end":140522211,"strand":1,"feature_type":"variation","start":140522211,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795886402","clinical_significance":[]},{"seq_region_name":"7","id":"rs1231832444","clinical_significance":[],"alleles":["GG","G"],"end":140522212,"strand":1,"feature_type":"variation","start":140522211,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1011585716","end":140522217,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140522217,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140522219,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522219,"clinical_significance":[],"seq_region_name":"7","id":"rs566338646"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140522220,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522220,"clinical_significance":[],"seq_region_name":"7","id":"rs539665559"},{"feature_type":"variation","strand":1,"end":140522222,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522222,"clinical_significance":[],"seq_region_name":"7","id":"rs558294595"},{"alleles":["CCAGGAGGAGGGTTACCCAGG","CCAGG"],"end":140522246,"strand":1,"feature_type":"variation","start":140522226,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1232519715","seq_region_name":"7","clinical_significance":[]},{"end":140522230,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140522230,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1329622599","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140522231,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522231,"clinical_significance":[],"seq_region_name":"7","id":"rs1289916725"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795887239","alleles":["G","A"],"end":140522233,"feature_type":"variation","strand":1,"source":"dbSNP","start":140522233,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795887321","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140522245,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522245,"source":"dbSNP"},{"id":"rs1407958692","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140522246,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522246,"source":"dbSNP"},{"id":"rs576873493","seq_region_name":"7","clinical_significance":[],"end":140522258,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140522258,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795887585","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140522261,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522261},{"id":"rs1795887673","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522268,"source":"dbSNP","strand":1,"feature_type":"variation","end":140522268,"alleles":["T","C"]},{"end":140522269,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140522269,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1032382010"},{"source":"dbSNP","start":140522270,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140522270,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs956916191"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522275,"feature_type":"variation","strand":1,"alleles":["TTTTTT","TTTTTTT"],"end":140522280,"clinical_significance":[],"seq_region_name":"7","id":"rs1795887973"},{"clinical_significance":[],"id":"rs928396319","seq_region_name":"7","source":"dbSNP","start":140522280,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140522280,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522282,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140522282,"seq_region_name":"7","id":"rs2130452353","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585542443","clinical_significance":[],"start":140522291,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140522291,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140522301,"alleles":["AAAAAA","AAAAA","AAAAAAA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522296,"source":"dbSNP","seq_region_name":"7","id":"rs1795888263","clinical_significance":[]},{"id":"rs770630830","seq_region_name":"7","clinical_significance":[],"start":140522298,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140522298,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1795888498","clinical_significance":[],"start":140522299,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140522299,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"alleles":["A","C","G"],"end":140522301,"strand":1,"feature_type":"variation","start":140522301,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1348424652","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522302,"feature_type":"variation","strand":1,"end":140522302,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1325491483"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522304,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140522304,"clinical_significance":[],"seq_region_name":"7","id":"rs1795888772"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522307,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140522307,"clinical_significance":[],"seq_region_name":"7","id":"rs1457904051"},{"end":140522308,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140522308,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs988732899","clinical_significance":[]},{"seq_region_name":"7","id":"rs960071092","clinical_significance":[],"start":140522309,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A","G"],"end":140522309,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1205766329","clinical_significance":[],"end":140522329,"alleles":["TTTTTATTTTGTTTTTATTTT","TTTTTATTTT"],"strand":1,"feature_type":"variation","start":140522309,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522310,"source":"dbSNP","strand":1,"feature_type":"variation","end":140522310,"alleles":["T","G"],"seq_region_name":"7","id":"rs1472577528","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795889376","feature_type":"variation","strand":1,"alleles":["TTTTATTTT","TTTT"],"end":140522318,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522310},{"seq_region_name":"7","id":"rs1795889455","clinical_significance":[],"start":140522326,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140522326,"strand":1,"feature_type":"variation"},{"end":140522331,"alleles":["TTTTTT","TTTTTTT"],"strand":1,"feature_type":"variation","start":140522326,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1426444965","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140522334,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522334,"clinical_significance":[],"seq_region_name":"7","id":"rs1795889606"},{"clinical_significance":[],"seq_region_name":"7","id":"rs918062691","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140522336,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522336},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522341,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140522341,"seq_region_name":"7","id":"rs1563114833","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522342,"source":"dbSNP","strand":1,"feature_type":"variation","end":140522342,"alleles":["C","T"],"seq_region_name":"7","id":"rs1795889866","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130452515","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522344,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140522344},{"clinical_significance":[],"seq_region_name":"7","id":"rs971394385","end":140522348,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140522348,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130452531","source":"dbSNP","start":140522350,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140522350,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795890030","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522351,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TT","TTT"],"end":140522352},{"seq_region_name":"7","id":"rs373479115","clinical_significance":[],"alleles":["C","T"],"end":140522354,"strand":1,"feature_type":"variation","start":140522354,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795890214","clinical_significance":[],"alleles":["C","G"],"end":140522355,"strand":1,"feature_type":"variation","start":140522355,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1795890294","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522358,"feature_type":"variation","strand":1,"end":140522358,"alleles":["G","C"]},{"clinical_significance":[],"id":"rs1489165942","seq_region_name":"7","end":140522359,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140522359,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795890462","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522362,"source":"dbSNP","strand":1,"feature_type":"variation","end":140522362,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795890556","end":140522363,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140522363,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140522365,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140522365,"alleles":["G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795890630","clinical_significance":[]},{"start":140522369,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140522369,"alleles":["A","T"],"strand":1,"feature_type":"variation","id":"rs1795890729","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs991229508","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140522375,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522375,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140522376,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522376,"clinical_significance":[],"seq_region_name":"7","id":"rs1795890934"},{"strand":1,"feature_type":"variation","end":140522377,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522377,"source":"dbSNP","seq_region_name":"7","id":"rs915731740","clinical_significance":[]},{"clinical_significance":[],"id":"rs1465040461","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522387,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140522387},{"id":"rs1479839381","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140522390,"strand":1,"feature_type":"variation","start":140522390,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1269809664","seq_region_name":"7","source":"dbSNP","start":140522391,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140522391,"feature_type":"variation","strand":1},{"start":140522396,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140522396,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs1795891308","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140522399,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522399,"clinical_significance":[],"id":"rs543856217","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1181062887","source":"dbSNP","start":140522400,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140522400,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522401,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140522401,"seq_region_name":"7","id":"rs1795891567","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1418093194","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522402,"feature_type":"variation","strand":1,"end":140522402,"alleles":["C","T"]},{"strand":1,"feature_type":"variation","end":140522403,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522403,"source":"dbSNP","seq_region_name":"7","id":"rs555837939","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs779548670","alleles":["C","G","T"],"end":140522404,"feature_type":"variation","strand":1,"source":"dbSNP","start":140522404,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140522405,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522405,"source":"dbSNP","seq_region_name":"7","id":"rs1795892228","clinical_significance":[]},{"end":140522409,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140522409,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs768904940"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140522421,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522421,"source":"dbSNP","seq_region_name":"7","id":"rs1475934958","clinical_significance":[]},{"alleles":["A","G"],"end":140522431,"feature_type":"variation","strand":1,"source":"dbSNP","start":140522431,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs550455375","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1162161640","source":"dbSNP","start":140522433,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140522433,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522434,"source":"dbSNP","strand":1,"feature_type":"variation","end":140522434,"alleles":["C","T"],"id":"rs1302712931","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795892832","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140522437,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522437},{"alleles":["C","G","T"],"end":140522438,"strand":1,"feature_type":"variation","start":140522438,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs973761630","clinical_significance":[]},{"source":"dbSNP","start":140522439,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140522439,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs374678261"},{"seq_region_name":"7","id":"rs2130452806","clinical_significance":[],"start":140522440,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140522440,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140522442,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140522442,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795893136","seq_region_name":"7"},{"start":140522443,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140522443,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130452826","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140522451,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522451,"source":"dbSNP","seq_region_name":"7","id":"rs2130452833","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522452,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140522452,"clinical_significance":[],"seq_region_name":"7","id":"rs2130452838"},{"strand":1,"feature_type":"variation","end":140522454,"alleles":["T","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522454,"source":"dbSNP","seq_region_name":"7","id":"rs1360306094","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130452854","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140522455,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522455},{"seq_region_name":"7","id":"rs1795893313","clinical_significance":[],"strand":1,"feature_type":"variation","end":140522456,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522456,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1037482994","clinical_significance":[],"end":140522458,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140522458,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["C","T"],"end":140522462,"strand":1,"feature_type":"variation","start":140522462,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs541404304","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","A"],"end":140522463,"feature_type":"variation","strand":1,"source":"dbSNP","start":140522463,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1392761915"},{"id":"rs1192412497","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522464,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140522464},{"feature_type":"variation","strand":1,"end":140522465,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522465,"clinical_significance":[],"seq_region_name":"7","id":"rs929337767"},{"seq_region_name":"7","id":"rs1795893854","clinical_significance":[],"alleles":["C","T"],"end":140522467,"strand":1,"feature_type":"variation","start":140522467,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs374659972","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522470,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140522470},{"strand":1,"feature_type":"variation","end":140522471,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522471,"source":"dbSNP","id":"rs527548116","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1052048950","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522475,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140522475},{"feature_type":"variation","strand":1,"end":140522475,"alleles":["A","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522475,"clinical_significance":[],"seq_region_name":"7","id":"rs1795895971"},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140522486,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522486,"source":"dbSNP","seq_region_name":"7","id":"rs1563114908","clinical_significance":[]},{"seq_region_name":"7","id":"rs1256299941","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140522494,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522494,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1299709711","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522495,"source":"dbSNP","strand":1,"feature_type":"variation","end":140522495,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795896591","alleles":["G","A"],"end":140522500,"feature_type":"variation","strand":1,"source":"dbSNP","start":140522500,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795896748","clinical_significance":[],"start":140522502,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140522502,"alleles":["T","A","C"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140522503,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522503,"source":"dbSNP","seq_region_name":"7","id":"rs6464825","clinical_significance":[]},{"clinical_significance":[],"id":"rs543517665","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140522505,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522505},{"clinical_significance":[],"seq_region_name":"7","id":"rs1007892537","feature_type":"variation","strand":1,"end":140522506,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522506},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140522507,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522507,"source":"dbSNP","seq_region_name":"7","id":"rs1795897554","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795897710","clinical_significance":[],"start":140522509,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140522509,"strand":1,"feature_type":"variation"},{"id":"rs1795897854","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140522514,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522514,"source":"dbSNP"},{"id":"rs1038926557","seq_region_name":"7","clinical_significance":[],"end":140522515,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140522515,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795898160","alleles":["G","T"],"end":140522520,"feature_type":"variation","strand":1,"source":"dbSNP","start":140522520,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["A","G"],"end":140522524,"strand":1,"feature_type":"variation","start":140522524,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795898303","clinical_significance":[]},{"end":140522527,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140522527,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs899878995"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1356336283","feature_type":"variation","strand":1,"end":140522529,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522529},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522530,"feature_type":"variation","strand":1,"end":140522530,"alleles":["T","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795898788"},{"strand":1,"feature_type":"variation","end":140522532,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522532,"source":"dbSNP","id":"rs1585542878","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs547771434","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522533,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140522533},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795899310","feature_type":"variation","strand":1,"end":140522534,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522534},{"seq_region_name":"7","id":"rs1032280001","clinical_significance":[],"end":140522536,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140522536,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1291531676","clinical_significance":[],"alleles":["C","T"],"end":140522537,"strand":1,"feature_type":"variation","start":140522537,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522538,"source":"dbSNP","strand":1,"feature_type":"variation","end":140522538,"alleles":["T","C"],"seq_region_name":"7","id":"rs1795899781","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140522539,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522539,"clinical_significance":[],"seq_region_name":"7","id":"rs1795899907"},{"end":140522544,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140522544,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795900035","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522546,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140522546,"id":"rs1563114940","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795900320","feature_type":"variation","strand":1,"alleles":["T","-"],"end":140522546,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522546},{"end":140522547,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140522547,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585542916"},{"end":140522550,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140522550,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795900598"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522553,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140522553,"clinical_significance":[],"seq_region_name":"7","id":"rs1795900745"},{"seq_region_name":"7","id":"rs1011075246","clinical_significance":[],"start":140522559,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140522559,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140522560,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140522560,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795900900","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795901070","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522562,"feature_type":"variation","strand":1,"end":140522562,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs564261138","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140522565,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522565},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522566,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140522566,"clinical_significance":[],"id":"rs1009620240","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522574,"feature_type":"variation","strand":1,"end":140522574,"alleles":["A","G"],"clinical_significance":[],"id":"rs1795901493","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795901612","clinical_significance":[],"start":140522576,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140522576,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1021238918","clinical_significance":[],"end":140522587,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140522587,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1795901915","seq_region_name":"7","end":140522593,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140522593,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1275682094","clinical_significance":[],"start":140522594,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140522594,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522594,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","-"],"end":140522594,"seq_region_name":"7","id":"rs1563114955","clinical_significance":[]},{"start":140522600,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140522600,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1306172185","clinical_significance":[]},{"clinical_significance":[],"id":"rs1204868524","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522601,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140522601},{"source":"dbSNP","start":140522605,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140522605,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795902465"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795902616","feature_type":"variation","strand":1,"end":140522608,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522608},{"end":140522609,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140522609,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1486449305"},{"seq_region_name":"7","id":"rs1185269575","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140522610,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522610,"source":"dbSNP"},{"source":"dbSNP","start":140522614,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140522617,"alleles":["TTTT","TT"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1465007686","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522616,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140522616,"seq_region_name":"7","id":"rs114431160","clinical_significance":[]},{"end":140522618,"alleles":["A","G","T"],"strand":1,"feature_type":"variation","start":140522618,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1003767766","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795903345","source":"dbSNP","start":140522618,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","-"],"end":140522618,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522619,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140522619,"seq_region_name":"7","id":"rs1795903490","clinical_significance":[]},{"end":140522626,"alleles":["TTTTTTTT","TTTTTTT","TTTTTTTTT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140522619,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1172520711","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795903826","feature_type":"variation","strand":1,"alleles":["A","T"],"end":140522628,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522628},{"source":"dbSNP","start":140522629,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140522629,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1391698394"},{"clinical_significance":[],"seq_region_name":"7","id":"rs772610625","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522631,"feature_type":"variation","strand":1,"end":140522631,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs193278682","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522632,"source":"dbSNP","strand":1,"feature_type":"variation","end":140522632,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795904443","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522633,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140522633},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795904556","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522636,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140522636},{"clinical_significance":[],"id":"rs1795904645","seq_region_name":"7","source":"dbSNP","start":140522637,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140522637,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522638,"feature_type":"variation","strand":1,"end":140522639,"alleles":["TT","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1256621016"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522641,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140522641,"seq_region_name":"7","id":"rs1585543067","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522642,"feature_type":"variation","strand":1,"end":140522648,"alleles":["TCTGTCT","TCT"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795904923"},{"clinical_significance":[],"seq_region_name":"7","id":"rs568548378","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140522645,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522645},{"feature_type":"variation","strand":1,"end":140522649,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522649,"clinical_significance":[],"seq_region_name":"7","id":"rs926847398"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1409228032","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140522653,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522653},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522656,"feature_type":"variation","strand":1,"alleles":["TGGAGTG","TG"],"end":140522662,"clinical_significance":[],"id":"rs566472963","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795905450","alleles":["A","T"],"end":140522659,"feature_type":"variation","strand":1,"source":"dbSNP","start":140522659,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522661,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140522661,"id":"rs1174036480","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1279513502","clinical_significance":[],"strand":1,"feature_type":"variation","end":140522663,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522663,"source":"dbSNP"},{"id":"rs1795905751","seq_region_name":"7","clinical_significance":[],"end":140522664,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140522664,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1795905843","seq_region_name":"7","feature_type":"variation","strand":1,"end":140522665,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522665},{"id":"rs963063027","seq_region_name":"7","clinical_significance":[],"start":140522671,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140522671,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1416879440","clinical_significance":[],"end":140522674,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140522674,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs370658997","alleles":["C","T"],"end":140522677,"feature_type":"variation","strand":1,"source":"dbSNP","start":140522677,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140522678,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522678,"source":"dbSNP","seq_region_name":"7","id":"rs547739052","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795906398","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522680,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","TT"],"end":140522680},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140522683,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522683,"source":"dbSNP","seq_region_name":"7","id":"rs1585543184","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795906617","end":140522685,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140522685,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["A","C"],"end":140522689,"feature_type":"variation","strand":1,"source":"dbSNP","start":140522689,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1585543188","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522695,"source":"dbSNP","strand":1,"feature_type":"variation","end":140522695,"alleles":["G","C"],"id":"rs1272487834","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795906972","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522696,"source":"dbSNP","strand":1,"feature_type":"variation","end":140522696,"alleles":["C","A"]},{"seq_region_name":"7","id":"rs959693165","clinical_significance":[],"start":140522697,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140522697,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs758786317","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522701,"source":"dbSNP","strand":1,"feature_type":"variation","end":140522703,"alleles":["TAG","TAGTAG"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1315339770","end":140522704,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140522704,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140522709,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522709,"clinical_significance":[],"seq_region_name":"7","id":"rs991655205"},{"seq_region_name":"7","id":"rs1355458848","clinical_significance":[],"alleles":["C","T"],"end":140522710,"strand":1,"feature_type":"variation","start":140522710,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140522714,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140522714,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585543245","clinical_significance":[]},{"seq_region_name":"7","id":"rs929057950","clinical_significance":[],"end":140522715,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140522715,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs527238703","feature_type":"variation","strand":1,"end":140522717,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522717},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522721,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140522721,"clinical_significance":[],"id":"rs1309162131","seq_region_name":"7"},{"clinical_significance":[],"id":"rs111542697","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140522722,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522722},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522724,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140522724,"seq_region_name":"7","id":"rs1585543309","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1272485382","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522727,"feature_type":"variation","strand":1,"end":140522727,"alleles":["A","C"]},{"strand":1,"feature_type":"variation","end":140522730,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522730,"source":"dbSNP","seq_region_name":"7","id":"rs911754191","clinical_significance":[]},{"id":"rs1795908059","seq_region_name":"7","clinical_significance":[],"start":140522731,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140522731,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522732,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140522732,"clinical_significance":[],"id":"rs185628971","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795908251","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522733,"feature_type":"variation","strand":1,"end":140522733,"alleles":["G","A"]},{"id":"rs1360482784","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522734,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140522734},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522736,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140522736,"id":"rs1795908370","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs963568261","end":140522740,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140522740,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1228223087","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140522748,"strand":1,"feature_type":"variation","start":140522748,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795908673","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140522750,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522750},{"source":"dbSNP","start":140522752,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140522752,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1166735242"},{"seq_region_name":"7","id":"rs1038957788","clinical_significance":[],"end":140522753,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140522753,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs2130453774","seq_region_name":"7","clinical_significance":[],"start":140522755,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140522755,"strand":1,"feature_type":"variation"},{"start":140522757,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140522757,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs1182814412","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs760297083","alleles":["C","T"],"end":140522759,"feature_type":"variation","strand":1,"source":"dbSNP","start":140522759,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522760,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","T"],"end":140522760,"seq_region_name":"7","id":"rs973198090","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs768700218","feature_type":"variation","strand":1,"end":140522769,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522769},{"end":140522771,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140522771,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795909454"},{"seq_region_name":"7","id":"rs1795909534","clinical_significance":[],"alleles":["A","G","T"],"end":140522773,"strand":1,"feature_type":"variation","start":140522773,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140522774,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140522774,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795909659"},{"clinical_significance":[],"id":"rs1795909753","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522775,"feature_type":"variation","strand":1,"alleles":["TTTTT","TTTTTT"],"end":140522779},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140522780,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522780,"source":"dbSNP","seq_region_name":"7","id":"rs919064058","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140522796,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522796,"clinical_significance":[],"seq_region_name":"7","id":"rs1208314500"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1277454677","alleles":["G","A","T"],"end":140522797,"feature_type":"variation","strand":1,"source":"dbSNP","start":140522797,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522800,"feature_type":"variation","strand":1,"end":140522800,"alleles":["T","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130453888"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522804,"feature_type":"variation","strand":1,"end":140522804,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs929244470"},{"start":140522806,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140522806,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs1795910309","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140522808,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522808,"source":"dbSNP","seq_region_name":"7","id":"rs1795910425","clinical_significance":[]},{"seq_region_name":"7","id":"rs1243145690","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140522809,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522809,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1334627170","clinical_significance":[],"strand":1,"feature_type":"variation","end":140522810,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522810,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140522812,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522812,"source":"dbSNP","seq_region_name":"7","id":"rs987312065","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs911891562","source":"dbSNP","start":140522813,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140522813,"alleles":["G","A"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140522815,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140522815,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1000039766","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140522818,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522818,"source":"dbSNP","seq_region_name":"7","id":"rs1795911002","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130453975","clinical_significance":[],"end":140522821,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140522821,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585543482","source":"dbSNP","start":140522824,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140522824,"alleles":["T","G"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140522825,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522825,"source":"dbSNP","seq_region_name":"7","id":"rs1585543496","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522826,"source":"dbSNP","strand":1,"feature_type":"variation","end":140522833,"alleles":["TCGAACTC","TC"],"seq_region_name":"7","id":"rs1585543509","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs376616807","source":"dbSNP","start":140522827,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140522827,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs28384334","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522828,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140522828},{"seq_region_name":"7","id":"rs1326326584","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522830,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140522830},{"end":140522832,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140522832,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1390303525","clinical_significance":[]},{"clinical_significance":[],"id":"rs567336743","seq_region_name":"7","end":140522842,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140522842,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["G","A","T"],"end":140522844,"feature_type":"variation","strand":1,"source":"dbSNP","start":140522844,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1294935882","seq_region_name":"7"},{"seq_region_name":"7","id":"rs893870236","clinical_significance":[],"start":140522845,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A","G"],"end":140522845,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1795912228","seq_region_name":"7","source":"dbSNP","start":140522846,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140522846,"alleles":["G","A"],"feature_type":"variation","strand":1},{"start":140522851,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C","G"],"end":140522851,"strand":1,"feature_type":"variation","id":"rs1585543576","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522858,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140522858,"clinical_significance":[],"seq_region_name":"7","id":"rs1010103055"},{"strand":1,"feature_type":"variation","end":140522859,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522859,"source":"dbSNP","seq_region_name":"7","id":"rs765354285","clinical_significance":[]},{"seq_region_name":"7","id":"rs1473562359","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522860,"source":"dbSNP","strand":1,"feature_type":"variation","end":140522860,"alleles":["G","A"]},{"end":140522868,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140522868,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795912759","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1194133794","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522876,"feature_type":"variation","strand":1,"end":140522876,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1361968547","end":140522878,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140522878,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522879,"feature_type":"variation","strand":1,"end":140522879,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs537236966"},{"id":"rs1795913147","seq_region_name":"7","clinical_significance":[],"start":140522886,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140522886,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795913251","end":140522887,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140522887,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs2130454162","seq_region_name":"7","alleles":["C","A"],"end":140522893,"feature_type":"variation","strand":1,"source":"dbSNP","start":140522893,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130454169","end":140522895,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140522895,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140522897,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140522897,"strand":1,"feature_type":"variation","id":"rs1795913345","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1452239532","clinical_significance":[],"start":140522898,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140522898,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1432598758","alleles":["G","A","C"],"end":140522900,"feature_type":"variation","strand":1,"source":"dbSNP","start":140522900,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1269482580","clinical_significance":[],"start":140522901,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140522901,"strand":1,"feature_type":"variation"},{"start":140522904,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140522904,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs906722228","clinical_significance":[]},{"seq_region_name":"7","id":"rs1171087115","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140522906,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522906,"source":"dbSNP"},{"source":"dbSNP","start":140522907,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140522907,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs946901680","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1468164181","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["CACA","CA"],"end":140522910,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522907},{"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140522909,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522909,"clinical_significance":[],"seq_region_name":"7","id":"rs569068091"},{"id":"rs1042589910","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140522914,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522914,"source":"dbSNP"},{"source":"dbSNP","start":140522917,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140522917,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs765941416"},{"end":140522918,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140522918,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs902658927","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795914456","clinical_significance":[],"start":140522936,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140522936,"strand":1,"feature_type":"variation"},{"end":140522939,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140522939,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130454282","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522940,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140522940,"id":"rs1401753954","seq_region_name":"7","clinical_significance":[]},{"end":140522944,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140522944,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1401425107"},{"clinical_significance":[],"id":"rs1320373245","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522945,"feature_type":"variation","strand":1,"end":140522945,"alleles":["A","G"]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140522951,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522951,"clinical_significance":[],"seq_region_name":"7","id":"rs1002353515"},{"seq_region_name":"7","id":"rs1324698850","clinical_significance":[],"end":140522952,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140522952,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140522953,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140522953,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1435038871"},{"seq_region_name":"7","id":"rs1331180901","clinical_significance":[],"start":140522954,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140522956,"alleles":["CCC","CC"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585543791","source":"dbSNP","start":140522956,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140522956,"alleles":["C","T"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140522957,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522957,"source":"dbSNP","seq_region_name":"7","id":"rs1033825820","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140522959,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522959,"clinical_significance":[],"seq_region_name":"7","id":"rs61704926"},{"end":140522962,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140522962,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs963637401","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795915686","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140522963,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522963,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522969,"feature_type":"variation","strand":1,"end":140522969,"alleles":["A","G"],"clinical_significance":[],"id":"rs973619030","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795915892","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522973,"source":"dbSNP","strand":1,"feature_type":"variation","end":140522973,"alleles":["G","T"]},{"start":140522978,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140522978,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585543847","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795916077","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140522979,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140522979},{"seq_region_name":"7","id":"rs1795916236","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140522986,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140522986,"source":"dbSNP"},{"id":"rs1795916373","seq_region_name":"7","clinical_significance":[],"alleles":["T","-"],"end":140522991,"strand":1,"feature_type":"variation","start":140522991,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140522995,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140522995,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs146745843","clinical_significance":[]},{"start":140522996,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G","T"],"end":140522996,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs574166420","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1393252176","source":"dbSNP","start":140522997,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140522997,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795917027","source":"dbSNP","start":140522998,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140522998,"alleles":["C","A"],"feature_type":"variation","strand":1},{"alleles":["C","T"],"end":140522999,"feature_type":"variation","strand":1,"source":"dbSNP","start":140522999,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs950413409"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795917279","source":"dbSNP","start":140523001,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140523003,"alleles":["GGG","GG"],"feature_type":"variation","strand":1},{"end":140523002,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140523002,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1321023839","clinical_significance":[]},{"seq_region_name":"7","id":"rs759429439","clinical_significance":[],"alleles":["G","A"],"end":140523003,"strand":1,"feature_type":"variation","start":140523003,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795917733","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523004,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140523004},{"seq_region_name":"7","id":"rs535121776","clinical_significance":[],"start":140523007,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140523007,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs767513629","seq_region_name":"7","source":"dbSNP","start":140523009,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C","T"],"end":140523009,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795918220","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523010,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140523010},{"seq_region_name":"7","id":"rs1795918353","clinical_significance":[],"start":140523015,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140523015,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1382777923","end":140523016,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140523016,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140523030,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140523030,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1563115235","clinical_significance":[]},{"end":140523032,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140523032,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs553688576","clinical_significance":[]},{"alleles":["G","A"],"end":140523033,"feature_type":"variation","strand":1,"source":"dbSNP","start":140523033,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs752378977"},{"clinical_significance":[],"id":"rs1795919160","seq_region_name":"7","alleles":["G","T"],"end":140523035,"feature_type":"variation","strand":1,"source":"dbSNP","start":140523035,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140523042,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523042,"source":"dbSNP","id":"rs895505530","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","T"],"end":140523045,"strand":1,"feature_type":"variation","start":140523045,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130454585","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130454598","source":"dbSNP","start":140523046,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140523046,"feature_type":"variation","strand":1},{"end":140523048,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140523048,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130454607","clinical_significance":[]},{"id":"rs2130454613","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523049,"source":"dbSNP","strand":1,"feature_type":"variation","end":140523049,"alleles":["A","G"]},{"source":"dbSNP","start":140523050,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140523050,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795919465"},{"alleles":["G","A"],"end":140523051,"feature_type":"variation","strand":1,"source":"dbSNP","start":140523051,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795919618"},{"seq_region_name":"7","id":"rs911635095","clinical_significance":[],"strand":1,"feature_type":"variation","end":140523058,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523058,"source":"dbSNP"},{"seq_region_name":"7","id":"rs943230306","clinical_significance":[],"end":140523065,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140523065,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140523077,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140523077,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1563115251","seq_region_name":"7"},{"seq_region_name":"7","id":"rs974559931","clinical_significance":[],"end":140523081,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140523081,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140523082,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140523082,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs188007334","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523082,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","-"],"end":140523082,"seq_region_name":"7","id":"rs1191801297","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140523083,"alleles":["C","A","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523083,"source":"dbSNP","seq_region_name":"7","id":"rs1248873027","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140523088,"alleles":["CCCCCC","CCCCCCC"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523083,"source":"dbSNP","seq_region_name":"7","id":"rs1012582069","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795921003","alleles":["C","A"],"end":140523084,"feature_type":"variation","strand":1,"source":"dbSNP","start":140523084,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140523086,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523086,"clinical_significance":[],"seq_region_name":"7","id":"rs1023165190"},{"clinical_significance":[],"id":"rs546128418","seq_region_name":"7","end":140523088,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140523088,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1201560984","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523093,"feature_type":"variation","strand":1,"end":140523093,"alleles":["A","C"]},{"clinical_significance":[],"id":"rs1795921395","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523096,"feature_type":"variation","strand":1,"end":140523096,"alleles":["C","G"]},{"seq_region_name":"7","id":"rs1795921488","clinical_significance":[],"start":140523097,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140523097,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140523098,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140523098,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1206470072","seq_region_name":"7"},{"seq_region_name":"7","id":"rs140428189","clinical_significance":[],"end":140523101,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140523101,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140523108,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523108,"source":"dbSNP","seq_region_name":"7","id":"rs2130454782","clinical_significance":[]},{"end":140523110,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140523110,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1347698206","seq_region_name":"7"},{"clinical_significance":[],"id":"rs935920849","seq_region_name":"7","source":"dbSNP","start":140523112,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140523112,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs145617234","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140523115,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523115,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523118,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140523118,"id":"rs892495575","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795922158","source":"dbSNP","start":140523119,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140523119,"alleles":["G","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795922256","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523124,"source":"dbSNP","strand":1,"feature_type":"variation","end":140523124,"alleles":["G","T"]},{"id":"rs1369876887","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140523126,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523126,"source":"dbSNP"},{"alleles":["G","C"],"end":140523127,"strand":1,"feature_type":"variation","start":140523127,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795922450","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795922547","clinical_significance":[],"end":140523131,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140523131,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140523134,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140523134,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1585544235","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523150,"feature_type":"variation","strand":1,"end":140523150,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1026107952"},{"source":"dbSNP","start":140523153,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140523153,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs777285244","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795922920","clinical_significance":[],"start":140523163,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140523163,"strand":1,"feature_type":"variation"},{"start":140523167,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C"],"end":140523167,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs57124453","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523169,"source":"dbSNP","strand":1,"feature_type":"variation","end":140523169,"alleles":["T","A"],"seq_region_name":"7","id":"rs1795923124","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130454925","clinical_significance":[],"start":140523169,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140523184,"alleles":["TAAACAGAATGAGGCC","TAAACAGAATGAGGCCTAAACAGAATGAGGCC"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1464017778","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140523172,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523172},{"id":"rs1795923318","seq_region_name":"7","clinical_significance":[],"start":140523177,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140523177,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140523182,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523182,"source":"dbSNP","seq_region_name":"7","id":"rs1795923407","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130454943","clinical_significance":[],"alleles":["C","G"],"end":140523185,"strand":1,"feature_type":"variation","start":140523185,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1214288731","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140523188,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523188,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1046939965","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523192,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140523192},{"alleles":["C","G"],"end":140523194,"strand":1,"feature_type":"variation","start":140523194,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs906635249","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140523197,"alleles":["CC","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523196,"source":"dbSNP","id":"rs1795924026","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795924160","feature_type":"variation","strand":1,"end":140523201,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523201},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130454976","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523208,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140523208},{"alleles":["G","A"],"end":140523211,"strand":1,"feature_type":"variation","start":140523211,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1415017840","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs576342376","end":140523214,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140523214,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs6943477","clinical_significance":[],"start":140523215,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140523215,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1795924889","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523220,"feature_type":"variation","strand":1,"end":140523220,"alleles":["C","T"]},{"clinical_significance":[],"id":"rs1795925031","seq_region_name":"7","source":"dbSNP","start":140523223,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C","T"],"end":140523223,"feature_type":"variation","strand":1},{"end":140523224,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140523224,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1171920332","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1434165030","seq_region_name":"7","alleles":["G","A"],"end":140523227,"feature_type":"variation","strand":1,"source":"dbSNP","start":140523227,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs373226360","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523228,"source":"dbSNP","strand":1,"feature_type":"variation","end":140523228,"alleles":["G","A"]},{"alleles":["C","T"],"end":140523229,"strand":1,"feature_type":"variation","start":140523229,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs529370878","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140523234,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523234,"source":"dbSNP","id":"rs1795925679","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140523237,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140523237,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs974756095"},{"seq_region_name":"7","id":"rs1795925883","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523238,"source":"dbSNP","strand":1,"feature_type":"variation","end":140523238,"alleles":["A","G"]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140523240,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523240,"clinical_significance":[],"seq_region_name":"7","id":"rs1795925959"},{"source":"dbSNP","start":140523242,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140523242,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795926080"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523244,"feature_type":"variation","strand":1,"end":140523244,"alleles":["C","G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1241915341"},{"end":140523247,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140523247,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1188655941"},{"source":"dbSNP","start":140523252,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140523252,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1444676189"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523257,"source":"dbSNP","strand":1,"feature_type":"variation","end":140523257,"alleles":["A","C"],"seq_region_name":"7","id":"rs373822763","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140523258,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523258,"clinical_significance":[],"seq_region_name":"7","id":"rs749493186"},{"feature_type":"variation","strand":1,"end":140523259,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523259,"clinical_significance":[],"seq_region_name":"7","id":"rs1795926673"},{"clinical_significance":[],"id":"rs1379770937","seq_region_name":"7","end":140523261,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140523261,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1346545824","clinical_significance":[],"strand":1,"feature_type":"variation","end":140523262,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523262,"source":"dbSNP"},{"source":"dbSNP","start":140523263,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140523263,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1328440021"},{"alleles":["G","A"],"end":140523268,"strand":1,"feature_type":"variation","start":140523268,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1274649642","clinical_significance":[]},{"clinical_significance":[],"id":"rs2130455206","seq_region_name":"7","end":140523269,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140523269,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140523272,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523272,"source":"dbSNP","seq_region_name":"7","id":"rs1795927162","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs768941174","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523273,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140523273},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563115358","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140523281,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523281},{"consequence_type":"splice_donor_5th_base_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523282,"feature_type":"variation","strand":1,"end":140523303,"alleles":["CACTGGGAGGTGGCTGAACACT","CACT"],"clinical_significance":[],"seq_region_name":"7","id":"rs1563115361"},{"seq_region_name":"7","id":"rs1438024460","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140523283,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523283,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795927620","source":"dbSNP","start":140523288,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140523288,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs10273161","feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140523291,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523291},{"seq_region_name":"7","id":"rs1585544528","clinical_significance":[],"alleles":["T","G"],"end":140523292,"strand":1,"feature_type":"variation","start":140523292,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["G","A","C"],"end":140523293,"feature_type":"variation","strand":1,"source":"dbSNP","start":140523293,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs761954304"},{"id":"rs1585544536","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140523296,"strand":1,"feature_type":"variation","start":140523296,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs772107708","clinical_significance":[],"strand":1,"feature_type":"variation","end":140523297,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523297,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130455319","source":"dbSNP","start":140523297,"consequence_type":"splice_donor_5th_base_variant","assembly_name":"GRCh38","alleles":["GAACAC","-"],"end":140523302,"feature_type":"variation","strand":1},{"end":140523300,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140523300,"consequence_type":"splice_region_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1448470567"},{"clinical_significance":[],"id":"rs1585544564","seq_region_name":"7","consequence_type":"splice_donor_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523301,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140523301},{"clinical_significance":[],"id":"rs759241083","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["ACTTAC","ACTTACTTAC"],"end":140523306,"consequence_type":"splice_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523301},{"consequence_type":"splice_donor_5th_base_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523302,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140523302,"clinical_significance":[],"seq_region_name":"7","id":"rs1281877141"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795928657","end":140523303,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140523303,"consequence_type":"splice_donor_region_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1585544590","clinical_significance":[],"strand":1,"feature_type":"variation","end":140523305,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"splice_donor_variant","start":140523305,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["A","AA"],"end":140523305,"consequence_type":"splice_donor_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523305,"clinical_significance":[],"seq_region_name":"7","id":"rs1795928801"},{"clinical_significance":[],"id":"rs559651394","seq_region_name":"7","alleles":["C","G","T"],"end":140523307,"feature_type":"variation","strand":1,"source":"dbSNP","start":140523307,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"splice_region_variant","start":140523308,"source":"dbSNP","strand":1,"feature_type":"variation","end":140523308,"alleles":["G","A"],"id":"rs759517190","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs764986251","source":"dbSNP","start":140523310,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140523310,"alleles":["G","A","T"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140523311,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140523311,"source":"dbSNP","seq_region_name":"7","id":"rs1467108506","clinical_significance":[]},{"alleles":["C","T"],"end":140523315,"strand":1,"feature_type":"variation","start":140523315,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs752519297","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs762463828","source":"dbSNP","start":140523316,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140523316,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1471274918","consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523317,"feature_type":"variation","strand":1,"end":140523317,"alleles":["G","A"]},{"end":140523320,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140523320,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795929720"},{"feature_type":"variation","strand":1,"end":140523321,"alleles":["A","C"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523321,"clinical_significance":[],"id":"rs1175773822","seq_region_name":"7"},{"seq_region_name":"7","id":"rs778605332","clinical_significance":["uncertain significance"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140523322,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140523322},{"seq_region_name":"7","id":"rs1164268158","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140523323,"source":"dbSNP","strand":1,"feature_type":"variation","end":140523323,"alleles":["G","A","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs371547503","alleles":["G","A"],"end":140523325,"feature_type":"variation","strand":1,"source":"dbSNP","start":140523325,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130455514","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140523326,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523326},{"feature_type":"variation","strand":1,"end":140523328,"alleles":["C","G"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523328,"clinical_significance":[],"seq_region_name":"7","id":"rs756789377"},{"source":"dbSNP","start":140523331,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140523331,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs533169195"},{"source":"dbSNP","start":140523332,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","end":140523332,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs780910530"},{"feature_type":"variation","strand":1,"end":140523333,"alleles":["T","C"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523333,"clinical_significance":[],"id":"rs1322289751","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1056773766","clinical_significance":[],"start":140523337,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"stop_gained","end":140523337,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1795930791","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140523340,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140523340},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140523346,"source":"dbSNP","strand":1,"feature_type":"variation","end":140523346,"alleles":["C","T"],"id":"rs1251939512","seq_region_name":"7","clinical_significance":[]},{"start":140523347,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","alleles":["C","G"],"end":140523347,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs750946755","clinical_significance":[]},{"clinical_significance":[],"id":"rs756728721","seq_region_name":"7","source":"dbSNP","start":140523349,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140523349,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140523350,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140523350,"seq_region_name":"7","id":"rs1795931218","clinical_significance":[]},{"seq_region_name":"7","id":"rs895387304","clinical_significance":[],"end":140523352,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140523352,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"alleles":["G","A"],"end":140523353,"strand":1,"feature_type":"variation","start":140523353,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","id":"rs374442278","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140523356,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523356,"clinical_significance":[],"seq_region_name":"7","id":"rs1795931539"},{"start":140523374,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","alleles":["T","C"],"end":140523374,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795931626","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs368486455","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140523375,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523375},{"seq_region_name":"7","id":"rs1349520407","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140523380,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140523380},{"clinical_significance":[],"seq_region_name":"7","id":"rs1233632730","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140523382,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523382},{"alleles":["CC","C"],"end":140523386,"strand":1,"feature_type":"variation","start":140523385,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"frameshift_variant","seq_region_name":"7","id":"rs1294948018","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795932128","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523390,"feature_type":"variation","strand":1,"end":140523390,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563115550","end":140523393,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140523393,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"start":140523396,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140523396,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs768690238","clinical_significance":[]},{"seq_region_name":"7","id":"rs201046984","clinical_significance":["uncertain significance"],"start":140523397,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["G","A"],"end":140523397,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1262948665","clinical_significance":[],"alleles":["G","A"],"end":140523400,"strand":1,"feature_type":"variation","start":140523400,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523404,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140523404,"clinical_significance":[],"seq_region_name":"7","id":"rs994555289"},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140523405,"source":"dbSNP","strand":1,"feature_type":"variation","end":140523405,"alleles":["A","G"],"seq_region_name":"7","id":"rs1439572729","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140523406,"alleles":["T","A","C"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523406,"clinical_significance":[],"seq_region_name":"7","id":"rs748373537"},{"clinical_significance":[],"seq_region_name":"7","id":"rs772115351","feature_type":"variation","strand":1,"end":140523410,"alleles":["G","A"],"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523410},{"end":140523411,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140523411,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs571353919","clinical_significance":[]},{"end":140523415,"alleles":["TCCTC","TC"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140523411,"consequence_type":"inframe_deletion","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1300012793"},{"clinical_significance":["uncertain significance"],"seq_region_name":"7","id":"rs745399243","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140523418,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523418},{"id":"rs375396888","seq_region_name":"7","clinical_significance":[],"end":140523419,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140523419,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1416216441","end":140523423,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140523423,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs759429272","source":"dbSNP","start":140523424,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140523424,"alleles":["T","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs367934077","source":"dbSNP","start":140523427,"consequence_type":"splice_region_variant","assembly_name":"GRCh38","end":140523427,"alleles":["G","A"],"feature_type":"variation","strand":1},{"id":"rs1422288318","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"splice_region_variant","start":140523431,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140523431},{"seq_region_name":"7","id":"rs1563115619","clinical_significance":[],"start":140523441,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_polypyrimidine_tract_variant","end":140523441,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"id":"rs1585545029","seq_region_name":"7","clinical_significance":[],"start":140523442,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140523442,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"id":"rs775209372","seq_region_name":"7","clinical_significance":[],"end":140523443,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140523443,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1326317250","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140523444,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523444,"source":"dbSNP"},{"alleles":["T","C"],"end":140523452,"feature_type":"variation","strand":1,"source":"dbSNP","start":140523452,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1369522171"},{"clinical_significance":[],"seq_region_name":"7","id":"rs371749260","end":140523454,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140523454,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795934447","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523455,"source":"dbSNP","strand":1,"feature_type":"variation","end":140523457,"alleles":["GGG","GGGG"]},{"seq_region_name":"7","id":"rs772405732","clinical_significance":[],"strand":1,"feature_type":"variation","end":140523458,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523458,"source":"dbSNP"},{"seq_region_name":"7","id":"rs751214354","clinical_significance":[],"alleles":["C","T"],"end":140523460,"strand":1,"feature_type":"variation","start":140523460,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140523461,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140523461,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1243805668"},{"alleles":["G","A"],"end":140523464,"feature_type":"variation","strand":1,"source":"dbSNP","start":140523464,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1270639885","seq_region_name":"7"},{"seq_region_name":"7","id":"rs761425174","clinical_significance":[],"start":140523465,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140523465,"alleles":["G","A","C"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523466,"feature_type":"variation","strand":1,"end":140523466,"alleles":["C","A"],"clinical_significance":[],"id":"rs1212845441","seq_region_name":"7"},{"source":"dbSNP","start":140523468,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140523468,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130455904"},{"alleles":["C","T"],"end":140523469,"feature_type":"variation","strand":1,"source":"dbSNP","start":140523469,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1018996830"},{"seq_region_name":"7","id":"rs201080257","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523470,"source":"dbSNP","strand":1,"feature_type":"variation","end":140523470,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs749988704","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140523474,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523474,"source":"dbSNP"},{"source":"dbSNP","start":140523475,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140523475,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1255671931"},{"clinical_significance":[],"id":"rs756628386","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140523476,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523476},{"clinical_significance":[],"id":"rs1795935603","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140523478,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523478},{"end":140523483,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140523483,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1008669282"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585545210","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523486,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140523486},{"start":140523487,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140523487,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs112699797","clinical_significance":[]},{"alleles":["A","G"],"end":140523488,"strand":1,"feature_type":"variation","start":140523488,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs964670166","seq_region_name":"7","clinical_significance":[]},{"end":140523490,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140523490,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585545231"},{"source":"dbSNP","start":140523491,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140523491,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1469491713"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523495,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140523495,"seq_region_name":"7","id":"rs61677869","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140523499,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523499,"source":"dbSNP","id":"rs1795936461","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523500,"feature_type":"variation","strand":1,"end":140523500,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1212808446"},{"seq_region_name":"7","id":"rs1329851518","clinical_significance":[],"end":140523504,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140523504,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140523506,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140523506,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs935829474","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795936858","source":"dbSNP","start":140523507,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140523507,"alleles":["A","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795936938","source":"dbSNP","start":140523508,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140523508,"alleles":["G","A"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140523509,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523509,"clinical_significance":[],"seq_region_name":"7","id":"rs1795937033"},{"seq_region_name":"7","id":"rs1585545265","clinical_significance":[],"strand":1,"feature_type":"variation","end":140523515,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523515,"source":"dbSNP"},{"end":140523517,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140523517,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1362641219","clinical_significance":[]},{"end":140523518,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140523518,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795937368","clinical_significance":[]},{"source":"dbSNP","start":140523524,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140523524,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795937471"},{"id":"rs1585545298","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140523527,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523527,"source":"dbSNP"},{"end":140523529,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140523529,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795937629","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140523530,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523530,"clinical_significance":[],"id":"rs1795937770","seq_region_name":"7"},{"seq_region_name":"7","id":"rs915247096","clinical_significance":[],"start":140523531,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140523531,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"id":"rs1795938060","seq_region_name":"7","clinical_significance":[],"end":140523533,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140523533,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795938196","end":140523537,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140523537,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795938331","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523542,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140523542},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795938500","source":"dbSNP","start":140523543,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140523543,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523545,"feature_type":"variation","strand":1,"end":140523545,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1372711408"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795938613","end":140523547,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140523547,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs549132262","feature_type":"variation","strand":1,"end":140523556,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523556},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795938811","feature_type":"variation","strand":1,"alleles":["T","A"],"end":140523560,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523560},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523563,"source":"dbSNP","strand":1,"feature_type":"variation","end":140523563,"alleles":["G","A"],"seq_region_name":"7","id":"rs1795938910","clinical_significance":[]},{"seq_region_name":"7","id":"rs1250997227","clinical_significance":[],"strand":1,"feature_type":"variation","end":140523567,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523567,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140523572,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523572,"source":"dbSNP","id":"rs1275476480","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs989162584","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523573,"feature_type":"variation","strand":1,"end":140523573,"alleles":["T","A","C"]},{"start":140523576,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140523576,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs538967088","clinical_significance":[]},{"start":140523579,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140523579,"alleles":["G","-"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1325727677","clinical_significance":[]},{"alleles":["A","C"],"end":140523583,"feature_type":"variation","strand":1,"source":"dbSNP","start":140523583,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585545360"},{"strand":1,"feature_type":"variation","end":140523584,"alleles":["-","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523585,"source":"dbSNP","id":"rs1554458327","seq_region_name":"7","clinical_significance":[]},{"end":140523594,"alleles":["TTTTTTTTTT","TTTTTTTT","TTTTTTTTT","TTTTTTTTTTT"],"strand":1,"feature_type":"variation","start":140523585,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs35942512","clinical_significance":[]},{"clinical_significance":[],"id":"rs1400594800","seq_region_name":"7","feature_type":"variation","strand":1,"end":140523586,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523586},{"seq_region_name":"7","id":"rs949983850","clinical_significance":[],"strand":1,"feature_type":"variation","end":140523587,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523587,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523588,"source":"dbSNP","strand":1,"feature_type":"variation","end":140523588,"alleles":["T","A"],"seq_region_name":"7","id":"rs567825641","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795940144","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523590,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140523590},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140523592,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523592,"clinical_significance":[],"seq_region_name":"7","id":"rs939523099"},{"id":"rs1795940335","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140523595,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523595,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1795940435","seq_region_name":"7","end":140523596,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140523596,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140523597,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140523597,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795940536","clinical_significance":[]},{"end":140523603,"alleles":["AGAG","AG"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140523600,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795940640","seq_region_name":"7"},{"start":140523610,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140523610,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1455336191","clinical_significance":[]},{"id":"rs1250751106","seq_region_name":"7","clinical_significance":[],"start":140523612,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140523613,"alleles":["TT","-"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140523613,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523613,"source":"dbSNP","id":"rs1795940908","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523614,"source":"dbSNP","strand":1,"feature_type":"variation","end":140523614,"alleles":["G","A"],"id":"rs1056648131","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130456358","clinical_significance":[],"alleles":["T","G"],"end":140523615,"strand":1,"feature_type":"variation","start":140523615,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs77320856","feature_type":"variation","strand":1,"end":140523616,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523616},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523617,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140523617,"id":"rs906500172","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140523618,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140523618,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs180866911","seq_region_name":"7"},{"alleles":["A","G"],"end":140523619,"strand":1,"feature_type":"variation","start":140523619,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1055212473","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140523620,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523620,"source":"dbSNP","seq_region_name":"7","id":"rs572050247","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523630,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140523630,"seq_region_name":"7","id":"rs1795941657","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1236578517","alleles":["T","A"],"end":140523635,"feature_type":"variation","strand":1,"source":"dbSNP","start":140523635,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1165756674","clinical_significance":[],"end":140523639,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140523639,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1795941957","seq_region_name":"7","source":"dbSNP","start":140523640,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140523640,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795942057","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523646,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140523646},{"seq_region_name":"7","id":"rs1302963027","clinical_significance":[],"strand":1,"feature_type":"variation","end":140523656,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523656,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs899367450","source":"dbSNP","start":140523657,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140523657,"alleles":["A","G"],"feature_type":"variation","strand":1},{"id":"rs1585545557","seq_region_name":"7","clinical_significance":[],"start":140523658,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140523658,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523660,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140523660,"clinical_significance":[],"seq_region_name":"7","id":"rs1795942434"},{"seq_region_name":"7","id":"rs994992478","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523662,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140523662},{"alleles":["C","A"],"end":140523665,"feature_type":"variation","strand":1,"source":"dbSNP","start":140523665,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1436000361","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1420045728","clinical_significance":[],"alleles":["C","T"],"end":140523670,"strand":1,"feature_type":"variation","start":140523670,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs572405610","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523671,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140523671},{"clinical_significance":[],"seq_region_name":"7","id":"rs1048474522","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523672,"feature_type":"variation","strand":1,"end":140523672,"alleles":["G","T"]},{"feature_type":"variation","strand":1,"end":140523674,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523674,"clinical_significance":[],"seq_region_name":"7","id":"rs1795942999"},{"seq_region_name":"7","id":"rs1795943256","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523679,"source":"dbSNP","strand":1,"feature_type":"variation","end":140523679,"alleles":["G","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795943397","feature_type":"variation","strand":1,"end":140523682,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523682},{"clinical_significance":[],"id":"rs1795943555","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523683,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140523683},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795943677","source":"dbSNP","start":140523684,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140523684,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs539051117","feature_type":"variation","strand":1,"end":140523687,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523687},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523688,"feature_type":"variation","strand":1,"end":140523688,"alleles":["C","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1563115755"},{"source":"dbSNP","start":140523691,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140523691,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1163145774","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140523700,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523700,"source":"dbSNP","id":"rs1795944271","seq_region_name":"7","clinical_significance":[]},{"id":"rs868157613","seq_region_name":"7","clinical_significance":[],"end":140523707,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140523707,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140523709,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523709,"source":"dbSNP","seq_region_name":"7","id":"rs1392658936","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523712,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140523712,"clinical_significance":[],"seq_region_name":"7","id":"rs1172631519"},{"feature_type":"variation","strand":1,"end":140523715,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523715,"clinical_significance":[],"id":"rs1428709087","seq_region_name":"7"},{"alleles":["C","A","T"],"end":140523719,"feature_type":"variation","strand":1,"source":"dbSNP","start":140523719,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs764048964","seq_region_name":"7"},{"alleles":["G","A","T"],"end":140523720,"feature_type":"variation","strand":1,"source":"dbSNP","start":140523720,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs558109127"},{"source":"dbSNP","start":140523721,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140523721,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1485528067","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523722,"feature_type":"variation","strand":1,"end":140523722,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs751449077"},{"clinical_significance":[],"seq_region_name":"7","id":"rs995913855","feature_type":"variation","strand":1,"end":140523729,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523729},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523730,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140523730,"clinical_significance":[],"id":"rs576375103","seq_region_name":"7"},{"start":140523733,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140523733,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1414947042","clinical_significance":[]},{"id":"rs2130456711","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140523735,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523735,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795945985","source":"dbSNP","start":140523738,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140523738,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs957224576","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523744,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140523744},{"source":"dbSNP","start":140523749,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C","G"],"end":140523749,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1309460800"},{"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140523751,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523751,"clinical_significance":[],"seq_region_name":"7","id":"rs1294611332"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140523757,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523757,"source":"dbSNP","seq_region_name":"7","id":"rs898871860","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140523759,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523759,"source":"dbSNP","seq_region_name":"7","id":"rs1382005398","clinical_significance":[]},{"start":140523760,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140523760,"alleles":["G","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795946607","clinical_significance":[]},{"seq_region_name":"7","id":"rs542582094","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523764,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140523764},{"clinical_significance":[],"seq_region_name":"7","id":"rs1251784194","source":"dbSNP","start":140523766,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140523766,"alleles":["T","G"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523768,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140523768,"seq_region_name":"7","id":"rs2130456802","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140523774,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523774,"clinical_significance":[],"seq_region_name":"7","id":"rs1795946890"},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140523775,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523775,"source":"dbSNP","seq_region_name":"7","id":"rs1795946952","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795947069","clinical_significance":[],"alleles":["G","A"],"end":140523779,"strand":1,"feature_type":"variation","start":140523779,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140523784,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523784,"source":"dbSNP","seq_region_name":"7","id":"rs1341268249","clinical_significance":[]},{"clinical_significance":[],"id":"rs1795947268","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523787,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140523787},{"seq_region_name":"7","id":"rs1315374835","clinical_significance":[],"start":140523792,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G","T"],"end":140523792,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523793,"source":"dbSNP","strand":1,"feature_type":"variation","end":140523793,"alleles":["G","A"],"seq_region_name":"7","id":"rs913026990","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523798,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140523798,"id":"rs1373126459","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1193856012","seq_region_name":"7","source":"dbSNP","start":140523803,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140523803,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795947736","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523806,"feature_type":"variation","strand":1,"end":140523806,"alleles":["C","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795947826","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523807,"feature_type":"variation","strand":1,"end":140523807,"alleles":["A","G"]},{"clinical_significance":[],"id":"rs1585545881","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523807,"feature_type":"variation","strand":1,"end":140523808,"alleles":["AG","-"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1311696663","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140523815,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523815},{"clinical_significance":[],"id":"rs185288714","seq_region_name":"7","alleles":["G","A"],"end":140523816,"feature_type":"variation","strand":1,"source":"dbSNP","start":140523816,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795948193","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523817,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140523817},{"seq_region_name":"7","id":"rs1795948308","clinical_significance":[],"start":140523821,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140523821,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523824,"source":"dbSNP","strand":1,"feature_type":"variation","end":140523824,"alleles":["T","C"],"seq_region_name":"7","id":"rs1585545928","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140523825,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523825,"clinical_significance":[],"seq_region_name":"7","id":"rs981727198"},{"seq_region_name":"7","id":"rs1374407230","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523826,"source":"dbSNP","strand":1,"feature_type":"variation","end":140523826,"alleles":["G","C","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523828,"feature_type":"variation","strand":1,"end":140523828,"alleles":["C","T"],"clinical_significance":[],"id":"rs1795948682","seq_region_name":"7"},{"alleles":["C","T"],"end":140523832,"feature_type":"variation","strand":1,"source":"dbSNP","start":140523832,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795948773"},{"alleles":["A","G"],"end":140523834,"feature_type":"variation","strand":1,"source":"dbSNP","start":140523834,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs927990753"},{"seq_region_name":"7","id":"rs1795948937","clinical_significance":[],"end":140523840,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140523840,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795949030","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523841,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140523841},{"alleles":["TA","-"],"end":140523847,"feature_type":"variation","strand":1,"source":"dbSNP","start":140523846,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130456987"},{"seq_region_name":"7","id":"rs574182696","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523848,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140523848},{"feature_type":"variation","strand":1,"end":140523853,"alleles":["AGGCG","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523849,"clinical_significance":[],"seq_region_name":"7","id":"rs2130457003"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523852,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140523852,"clinical_significance":[],"seq_region_name":"7","id":"rs372239292"},{"start":140523853,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140523853,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs559583645","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["-","TGAGGCCAGGAGTTTGAGACCGGCCTGGGCAACATA","TGAGGCCAGGAGTTTGAGACCGGCCTGGGCAACATAGTGA"],"end":140523854,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523855,"source":"dbSNP","id":"rs1188866928","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795949590","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140523855,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523855,"source":"dbSNP"},{"clinical_significance":[],"id":"rs2130457046","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523856,"feature_type":"variation","strand":1,"alleles":["AGC","-"],"end":140523858},{"seq_region_name":"7","id":"rs1795949676","clinical_significance":[],"strand":1,"feature_type":"variation","end":140523862,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523862,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795949756","clinical_significance":[],"start":140523866,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140523866,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1190015334","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523867,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140523867},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523872,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140523872,"seq_region_name":"7","id":"rs886173804","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140523873,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523873,"source":"dbSNP","seq_region_name":"7","id":"rs188736899","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795950176","clinical_significance":[],"start":140523876,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140523876,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523880,"source":"dbSNP","strand":1,"feature_type":"variation","end":140523880,"alleles":["C","T"],"id":"rs1018799496","seq_region_name":"7","clinical_significance":[]},{"end":140523890,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140523890,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585546041","clinical_significance":[]},{"seq_region_name":"7","id":"rs920661752","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140523894,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523894,"source":"dbSNP"},{"source":"dbSNP","start":140523895,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140523895,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795950552","seq_region_name":"7"},{"source":"dbSNP","start":140523895,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140523897,"alleles":["GGG","GG"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795950683"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523899,"source":"dbSNP","strand":1,"feature_type":"variation","end":140523899,"alleles":["G","A"],"id":"rs1249824559","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523900,"source":"dbSNP","strand":1,"feature_type":"variation","end":140523900,"alleles":["C","A"],"id":"rs1226900377","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140523903,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523903,"source":"dbSNP","seq_region_name":"7","id":"rs1322702830","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs6963892","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140523904,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523904},{"feature_type":"variation","strand":1,"end":140523910,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523910,"clinical_significance":[],"seq_region_name":"7","id":"rs1795951483"},{"feature_type":"variation","strand":1,"end":140523914,"alleles":["CCAC","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523911,"clinical_significance":[],"seq_region_name":"7","id":"rs1374130070"},{"source":"dbSNP","start":140523912,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140523912,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1355363321"},{"source":"dbSNP","start":140523915,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140523915,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795951949"},{"end":140523917,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140523917,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs780040892"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130457231","source":"dbSNP","start":140523919,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140523919,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1311791206","seq_region_name":"7","end":140523923,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140523923,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1795952412","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523930,"feature_type":"variation","strand":1,"end":140523930,"alleles":["C","G"]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140523935,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523935,"source":"dbSNP","seq_region_name":"7","id":"rs1795952547","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795952678","alleles":["C","T"],"end":140523939,"feature_type":"variation","strand":1,"source":"dbSNP","start":140523939,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140523941,"alleles":["G","C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140523941,"clinical_significance":[],"id":"rs1047897086","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795953013","clinical_significance":[],"strand":1,"feature_type":"variation","end":140523943,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523943,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1795953168","clinical_significance":[],"start":140523951,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140523951,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"start":140523952,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140523952,"strand":1,"feature_type":"variation","id":"rs1795953326","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs886566065","clinical_significance":[],"alleles":["T","G"],"end":140523958,"strand":1,"feature_type":"variation","start":140523958,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1795953636","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140523959,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523959,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795953787","source":"dbSNP","start":140523962,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140523962,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1397934794","alleles":["T","C"],"end":140523963,"feature_type":"variation","strand":1,"source":"dbSNP","start":140523963,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523966,"source":"dbSNP","strand":1,"feature_type":"variation","end":140523966,"alleles":["A","AA"],"seq_region_name":"7","id":"rs200895236","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs563654637","end":140523967,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140523967,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140523970,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140523970,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs752745426","seq_region_name":"7"},{"source":"dbSNP","start":140523973,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140523973,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1166799057"},{"clinical_significance":[],"id":"rs1795954804","seq_region_name":"7","end":140523977,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140523977,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795954953","end":140523979,"alleles":["T","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140523979,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1795955148","clinical_significance":[],"strand":1,"feature_type":"variation","end":140523980,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140523980,"source":"dbSNP"},{"source":"dbSNP","start":140523990,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140523990,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs760372918","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524002,"source":"dbSNP","strand":1,"feature_type":"variation","end":140524002,"alleles":["G","A"],"seq_region_name":"7","id":"rs1314284362","clinical_significance":[]},{"clinical_significance":[],"id":"rs1376387049","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524004,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140524004},{"alleles":["C","G"],"end":140524007,"feature_type":"variation","strand":1,"source":"dbSNP","start":140524007,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1394921654"},{"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140524008,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524008,"clinical_significance":[],"seq_region_name":"7","id":"rs1420973348"},{"feature_type":"variation","strand":1,"end":140524011,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524011,"clinical_significance":[],"seq_region_name":"7","id":"rs114023627"},{"clinical_significance":[],"seq_region_name":"7","id":"rs149587455","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140524012,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524012},{"start":140524014,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","-"],"end":140524014,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1469037738","clinical_significance":[]},{"seq_region_name":"7","id":"rs1328138300","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524017,"source":"dbSNP","strand":1,"feature_type":"variation","end":140524017,"alleles":["G","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524019,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TTT","TTTT"],"end":140524021,"seq_region_name":"7","id":"rs1795956629","clinical_significance":[]},{"end":140524023,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140524023,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795956786","clinical_significance":[]},{"id":"rs1795956943","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524028,"source":"dbSNP","strand":1,"feature_type":"variation","end":140524028,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1275499128","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524035,"source":"dbSNP","strand":1,"feature_type":"variation","end":140524035,"alleles":["C","A"]},{"alleles":["G","A"],"end":140524037,"strand":1,"feature_type":"variation","start":140524037,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795957216","clinical_significance":[]},{"seq_region_name":"7","id":"rs1212182573","clinical_significance":[],"alleles":["G","A","T"],"end":140524041,"strand":1,"feature_type":"variation","start":140524041,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524045,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140524045,"clinical_significance":[],"seq_region_name":"7","id":"rs1795957446"},{"clinical_significance":[],"seq_region_name":"7","id":"rs763998156","feature_type":"variation","strand":1,"end":140524048,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524048},{"clinical_significance":[],"seq_region_name":"7","id":"rs1289513245","alleles":["G","A"],"end":140524051,"feature_type":"variation","strand":1,"source":"dbSNP","start":140524051,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524063,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140524063,"seq_region_name":"7","id":"rs1030978586","clinical_significance":[]},{"alleles":["C","G"],"end":140524064,"strand":1,"feature_type":"variation","start":140524064,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795958036","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140524066,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524066,"clinical_significance":[],"id":"rs2130457610","seq_region_name":"7"},{"source":"dbSNP","start":140524067,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C","T"],"end":140524067,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs960799507"},{"start":140524076,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140524076,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs992611997","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795958400","clinical_significance":[],"end":140524080,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140524080,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140524080,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140524082,"alleles":["GGG","GGGG"],"strand":1,"feature_type":"variation","id":"rs35511466","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524088,"feature_type":"variation","strand":1,"end":140524088,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1390510013"},{"clinical_significance":[],"id":"rs957131058","seq_region_name":"7","alleles":["G","T"],"end":140524089,"feature_type":"variation","strand":1,"source":"dbSNP","start":140524089,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1795958974","seq_region_name":"7","end":140524092,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140524092,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1371237301","alleles":["G","C"],"end":140524093,"feature_type":"variation","strand":1,"source":"dbSNP","start":140524093,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140524094,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140524094,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs2130457693","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130457703","source":"dbSNP","start":140524101,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140524101,"alleles":["T","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130457712","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524106,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140524106},{"id":"rs1327747077","seq_region_name":"7","clinical_significance":[],"alleles":["C","G","T"],"end":140524110,"strand":1,"feature_type":"variation","start":140524110,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140524114,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140524116,"alleles":["GGG","GGGG"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs35676689","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","-"],"end":140524120,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524120,"source":"dbSNP","seq_region_name":"7","id":"rs1795959594","clinical_significance":[]},{"start":140524120,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140524120,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130457738","clinical_significance":[]},{"id":"rs1795959744","seq_region_name":"7","clinical_significance":[],"start":140524122,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140524122,"strand":1,"feature_type":"variation"},{"end":140524130,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140524130,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795959894"},{"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140524131,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524131,"source":"dbSNP","id":"rs1459664271","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795960221","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524132,"feature_type":"variation","strand":1,"end":140524132,"alleles":["C","G"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524133,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140524133,"seq_region_name":"7","id":"rs1795960375","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["GGG","GG"],"end":140524139,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524137,"source":"dbSNP","id":"rs747209076","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140524139,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524139,"source":"dbSNP","seq_region_name":"7","id":"rs1010368574","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140524145,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524145,"clinical_significance":[],"seq_region_name":"7","id":"rs1020119351"},{"clinical_significance":[],"id":"rs971636211","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524146,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140524146},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140524150,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524150,"source":"dbSNP","seq_region_name":"7","id":"rs1795961129","clinical_significance":[]},{"clinical_significance":[],"id":"rs1273682303","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140524152,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524152},{"alleles":["C","G"],"end":140524156,"feature_type":"variation","strand":1,"source":"dbSNP","start":140524156,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795961437"},{"seq_region_name":"7","id":"rs1795961564","clinical_significance":[],"start":140524160,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140524160,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs948210571","clinical_significance":[],"start":140524164,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140524164,"strand":1,"feature_type":"variation"},{"id":"rs1181152020","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524168,"source":"dbSNP","strand":1,"feature_type":"variation","end":140524168,"alleles":["T","A","C"]},{"end":140524169,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140524169,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1454904515","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524182,"feature_type":"variation","strand":1,"end":140524182,"alleles":["T","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795962160"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524189,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140524189,"seq_region_name":"7","id":"rs1795962287","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524189,"feature_type":"variation","strand":1,"end":140524194,"alleles":["AAAAAA","AAAAAAA"],"clinical_significance":[],"seq_region_name":"7","id":"rs749541376"},{"end":140524194,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140524194,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1192219244"},{"alleles":["C","T"],"end":140524195,"feature_type":"variation","strand":1,"source":"dbSNP","start":140524195,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs73485769"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1285340145","end":140524196,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140524196,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524197,"feature_type":"variation","strand":1,"end":140524197,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1207428576"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140524199,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524199,"clinical_significance":[],"seq_region_name":"7","id":"rs1349129443"},{"start":140524201,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140524201,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs927184530","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140524205,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524205,"clinical_significance":[],"seq_region_name":"7","id":"rs1795963493"},{"alleles":["T","C"],"end":140524216,"strand":1,"feature_type":"variation","start":140524216,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1258475656","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140524218,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524218,"clinical_significance":[],"seq_region_name":"7","id":"rs1795963770"},{"clinical_significance":[],"seq_region_name":"7","id":"rs959387071","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524221,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140524221},{"end":140524222,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140524222,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795964059","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs6948786","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524224,"feature_type":"variation","strand":1,"end":140524224,"alleles":["A","G"]},{"clinical_significance":[],"id":"rs1795964513","seq_region_name":"7","alleles":["G","-"],"end":140524226,"feature_type":"variation","strand":1,"source":"dbSNP","start":140524226,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140524230,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524230,"source":"dbSNP","seq_region_name":"7","id":"rs375048685","clinical_significance":[]},{"source":"dbSNP","start":140524232,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140524232,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1047401852","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1482351927","alleles":["C","T"],"end":140524233,"feature_type":"variation","strand":1,"source":"dbSNP","start":140524233,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1438176881","source":"dbSNP","start":140524234,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140524234,"alleles":["A","AA"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795965121","clinical_significance":[],"start":140524234,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140524234,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs920567077","alleles":["C","T"],"end":140524235,"feature_type":"variation","strand":1,"source":"dbSNP","start":140524235,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["G","A"],"end":140524239,"strand":1,"feature_type":"variation","start":140524239,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795965400","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524242,"source":"dbSNP","strand":1,"feature_type":"variation","end":140524242,"alleles":["G","C"],"seq_region_name":"7","id":"rs1795965518","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524243,"feature_type":"variation","strand":1,"end":140524243,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1383903081"},{"alleles":["T","C"],"end":140524246,"strand":1,"feature_type":"variation","start":140524246,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795965826","clinical_significance":[]},{"end":140524251,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140524251,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs930745545","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585546745","clinical_significance":[],"strand":1,"feature_type":"variation","end":140524252,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524252,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524258,"feature_type":"variation","strand":1,"end":140524258,"alleles":["C","T"],"clinical_significance":[],"id":"rs369020043","seq_region_name":"7"},{"id":"rs1795966418","seq_region_name":"7","clinical_significance":[],"start":140524259,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140524259,"strand":1,"feature_type":"variation"},{"id":"rs1048273104","seq_region_name":"7","clinical_significance":[],"end":140524261,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140524261,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585546777","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140524264,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524264},{"seq_region_name":"7","id":"rs1158138820","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524267,"source":"dbSNP","strand":1,"feature_type":"variation","end":140524267,"alleles":["A","T"]},{"start":140524271,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140524271,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795966995","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140524280,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524280,"source":"dbSNP","seq_region_name":"7","id":"rs1795967141","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140524281,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524281,"clinical_significance":[],"id":"rs756926839","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524282,"feature_type":"variation","strand":1,"alleles":["TATAATTA","TATAATTATAATTA"],"end":140524289,"clinical_significance":[],"id":"rs1795967429","seq_region_name":"7"},{"clinical_significance":[],"id":"rs886085408","seq_region_name":"7","alleles":["A","G"],"end":140524283,"feature_type":"variation","strand":1,"source":"dbSNP","start":140524283,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795967722","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140524284,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524284},{"seq_region_name":"7","id":"rs1795967867","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524289,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140524289},{"feature_type":"variation","strand":1,"end":140524291,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524291,"clinical_significance":[],"seq_region_name":"7","id":"rs1585546801"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130458215","end":140524297,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140524297,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140524298,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524298,"clinical_significance":[],"id":"rs1172037349","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140524301,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524301,"source":"dbSNP","seq_region_name":"7","id":"rs944854710","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524306,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140524306,"seq_region_name":"7","id":"rs1430823204","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795968601","end":140524316,"alleles":["AGTTAG","AG"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140524311,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140524312,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524312,"clinical_significance":[],"id":"rs1040628158","seq_region_name":"7"},{"alleles":["G","A"],"end":140524316,"strand":1,"feature_type":"variation","start":140524316,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795969064","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs900781866","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524317,"feature_type":"variation","strand":1,"alleles":["G","A","C","T"],"end":140524317},{"id":"rs1261624827","seq_region_name":"7","clinical_significance":[],"start":140524324,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140524324,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1212152203","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524325,"source":"dbSNP","strand":1,"feature_type":"variation","end":140524325,"alleles":["A","G"]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140524334,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524334,"clinical_significance":[],"seq_region_name":"7","id":"rs1347981897"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524341,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140524341,"clinical_significance":[],"seq_region_name":"7","id":"rs1795970166"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140524343,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524343,"clinical_significance":[],"seq_region_name":"7","id":"rs1795970304"},{"seq_region_name":"7","id":"rs932206413","clinical_significance":[],"start":140524344,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140524344,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1231655875","clinical_significance":[],"strand":1,"feature_type":"variation","end":140524349,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524349,"source":"dbSNP"},{"seq_region_name":"7","id":"rs748515451","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["TGTGTGT","TGTGT"],"end":140524355,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524349,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524356,"source":"dbSNP","strand":1,"feature_type":"variation","end":140524356,"alleles":["T","C"],"id":"rs1054055776","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140524358,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524358,"clinical_significance":[],"seq_region_name":"7","id":"rs111580214"},{"strand":1,"feature_type":"variation","end":140524360,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524360,"source":"dbSNP","seq_region_name":"7","id":"rs1795971071","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795971172","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524367,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140524367},{"seq_region_name":"7","id":"rs1795971269","clinical_significance":[],"alleles":["A","G"],"end":140524369,"strand":1,"feature_type":"variation","start":140524369,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs543487541","alleles":["A","G"],"end":140524373,"feature_type":"variation","strand":1,"source":"dbSNP","start":140524373,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1040495243","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140524376,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524376},{"source":"dbSNP","start":140524378,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140524379,"alleles":["AA","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795971581"},{"seq_region_name":"7","id":"rs547506017","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524380,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140524380},{"clinical_significance":[],"seq_region_name":"7","id":"rs749892589","source":"dbSNP","start":140524392,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140524392,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1175176112","source":"dbSNP","start":140524399,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140524399,"alleles":["T","-"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524401,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140524401,"seq_region_name":"7","id":"rs1415277005","clinical_significance":[]},{"source":"dbSNP","start":140524403,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140524403,"alleles":["T","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs372924618"},{"seq_region_name":"7","id":"rs1795972206","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140524406,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524406,"source":"dbSNP"},{"alleles":["T","C"],"end":140524407,"feature_type":"variation","strand":1,"source":"dbSNP","start":140524407,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795972294","seq_region_name":"7"},{"end":140524409,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140524409,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs996410661"},{"seq_region_name":"7","id":"rs1311119023","clinical_significance":[],"start":140524414,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140524414,"strand":1,"feature_type":"variation"},{"start":140524415,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140524415,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1434376918","clinical_significance":[]},{"source":"dbSNP","start":140524420,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140524420,"alleles":["T","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1020446144"},{"id":"rs1795972811","seq_region_name":"7","clinical_significance":[],"start":140524433,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140524433,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1795972903","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524434,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140524434},{"strand":1,"feature_type":"variation","end":140524437,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524437,"source":"dbSNP","id":"rs2130458548","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524442,"source":"dbSNP","strand":1,"feature_type":"variation","end":140524442,"alleles":["C","T"],"seq_region_name":"7","id":"rs907064533","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130458564","end":140524445,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140524445,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140524451,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524451,"clinical_significance":[],"seq_region_name":"7","id":"rs1420485260"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1170062251","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524455,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140524455},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524460,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140524460,"clinical_significance":[],"seq_region_name":"7","id":"rs1795973279"},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140524461,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524461,"clinical_significance":[],"seq_region_name":"7","id":"rs565619881"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140524463,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524463,"source":"dbSNP","seq_region_name":"7","id":"rs1372798678","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130458600","clinical_significance":[],"start":140524473,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","-"],"end":140524473,"strand":1,"feature_type":"variation"},{"end":140524474,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140524474,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795973585","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524475,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C","T"],"end":140524475,"seq_region_name":"7","id":"rs903760196","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130458639","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524475,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","-"],"end":140524475},{"clinical_significance":[],"id":"rs1486912502","seq_region_name":"7","source":"dbSNP","start":140524481,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140524481,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795973898","clinical_significance":[],"end":140524491,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140524491,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524492,"source":"dbSNP","strand":1,"feature_type":"variation","end":140524492,"alleles":["T","C"],"seq_region_name":"7","id":"rs1795973991","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524496,"feature_type":"variation","strand":1,"end":140524496,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795974093"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795974185","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524503,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140524503},{"alleles":["T","C"],"end":140524504,"feature_type":"variation","strand":1,"source":"dbSNP","start":140524504,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1259066949","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795974386","clinical_significance":[],"start":140524505,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140524505,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1288958355","clinical_significance":[],"alleles":["C","T"],"end":140524519,"strand":1,"feature_type":"variation","start":140524519,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1034163012","clinical_significance":[],"end":140524520,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140524520,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140524523,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524523,"source":"dbSNP","seq_region_name":"7","id":"rs958625782","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524524,"feature_type":"variation","strand":1,"end":140524524,"alleles":["G","A"],"clinical_significance":[],"id":"rs960662059","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795974917","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524526,"source":"dbSNP","strand":1,"feature_type":"variation","end":140524526,"alleles":["G","T"]},{"source":"dbSNP","start":140524526,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140524531,"alleles":["GCGCGC","GCGC"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795975001","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1386435429","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524527,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140524527},{"end":140524528,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140524528,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs992288523"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524529,"source":"dbSNP","strand":1,"feature_type":"variation","end":140524529,"alleles":["C","T"],"id":"rs1432855390","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524529,"feature_type":"variation","strand":1,"end":140524529,"alleles":["C","CAC"],"clinical_significance":[],"seq_region_name":"7","id":"rs1554458490"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524529,"feature_type":"variation","strand":1,"alleles":["CGCACACACGCACACACG","CGCACACACG","CGCACACACGCACACACGCACACACG"],"end":140524546,"clinical_significance":[],"id":"rs1024135016","seq_region_name":"7"},{"alleles":["G","A"],"end":140524530,"feature_type":"variation","strand":1,"source":"dbSNP","start":140524530,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs10277628"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524531,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140524531,"id":"rs1795975761","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140524537,"alleles":["CACACAC","CACACACAC","CACACACACAC"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524531,"clinical_significance":[],"seq_region_name":"7","id":"rs771973166"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140524532,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524532,"clinical_significance":[],"seq_region_name":"7","id":"rs1296742927"},{"clinical_significance":[],"id":"rs1371522532","seq_region_name":"7","end":140524533,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140524533,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140524534,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524534,"clinical_significance":[],"seq_region_name":"7","id":"rs1795976187"},{"seq_region_name":"7","id":"rs1396257136","clinical_significance":[],"alleles":["A","G"],"end":140524536,"strand":1,"feature_type":"variation","start":140524536,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["C","T"],"end":140524537,"strand":1,"feature_type":"variation","start":140524537,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1476497085","clinical_significance":[]},{"seq_region_name":"7","id":"rs377065258","clinical_significance":[],"end":140524539,"alleles":["CGC","C"],"strand":1,"feature_type":"variation","start":140524537,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140524538,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524538,"clinical_significance":[],"seq_region_name":"7","id":"rs6964876"},{"alleles":["C","A"],"end":140524541,"feature_type":"variation","strand":1,"source":"dbSNP","start":140524541,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs747603739"},{"start":140524544,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140524544,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585547262","clinical_significance":[]},{"alleles":["C","T"],"end":140524545,"feature_type":"variation","strand":1,"source":"dbSNP","start":140524545,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs983581257"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524546,"feature_type":"variation","strand":1,"alleles":["-","AT"],"end":140524545,"clinical_significance":[],"seq_region_name":"7","id":"rs2130458949"},{"clinical_significance":[],"id":"rs569973083","seq_region_name":"7","source":"dbSNP","start":140524546,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140524546,"alleles":["G","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1795977128","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524548,"source":"dbSNP","strand":1,"feature_type":"variation","end":140524548,"alleles":["A","T"]},{"start":140524551,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140524551,"alleles":["T","A"],"strand":1,"feature_type":"variation","id":"rs1206205558","seq_region_name":"7","clinical_significance":[]},{"start":140524552,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140524552,"strand":1,"feature_type":"variation","id":"rs907932365","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs944784363","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524553,"feature_type":"variation","strand":1,"end":140524553,"alleles":["C","A","T"]},{"feature_type":"variation","strand":1,"end":140524554,"alleles":["A","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524554,"clinical_significance":[],"seq_region_name":"7","id":"rs976233567"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524556,"feature_type":"variation","strand":1,"alleles":["A","-"],"end":140524556,"clinical_significance":[],"id":"rs1795977682","seq_region_name":"7"},{"source":"dbSNP","start":140524557,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140524564,"alleles":["TTTTTTTT","TTTTTTT","TTTTTTTTT","TTTTTTTTTT"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1207432385"},{"clinical_significance":[],"seq_region_name":"7","id":"rs76564869","alleles":["T","C"],"end":140524564,"feature_type":"variation","strand":1,"source":"dbSNP","start":140524564,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140524565,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524565,"source":"dbSNP","id":"rs1374186339","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140524570,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140524570,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1455020017"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524572,"source":"dbSNP","strand":1,"feature_type":"variation","end":140524572,"alleles":["C","T"],"seq_region_name":"7","id":"rs1281306429","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795979903","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524573,"feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140524573},{"clinical_significance":[],"seq_region_name":"7","id":"rs745984367","end":140524580,"alleles":["TCTCTCT","TCT","TCTCT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140524574,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140524577,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140524577,"strand":1,"feature_type":"variation","id":"rs1795980345","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795980504","feature_type":"variation","strand":1,"end":140524581,"alleles":["TCTT","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524578},{"seq_region_name":"7","id":"rs1795980676","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524578,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TCTTT","T"],"end":140524582},{"alleles":["T","C"],"end":140524580,"strand":1,"feature_type":"variation","start":140524580,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1164845065","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs900233387","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524580,"feature_type":"variation","strand":1,"end":140524589,"alleles":["TTTTTTTTTT","TTTTTTTT","TTTTTTTTT","TTTTTTTTTTT"]},{"source":"dbSNP","start":140524581,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140524581,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1795981337"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1401758375","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524582,"feature_type":"variation","strand":1,"end":140524582,"alleles":["T","C"]},{"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140524583,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524583,"clinical_significance":[],"seq_region_name":"7","id":"rs1795981584"},{"clinical_significance":[],"id":"rs1423434732","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524590,"feature_type":"variation","strand":1,"end":140524590,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1795981769","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524590,"source":"dbSNP","strand":1,"feature_type":"variation","end":140524590,"alleles":["C","-"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524591,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140524591,"seq_region_name":"7","id":"rs1178395718","clinical_significance":[]},{"seq_region_name":"7","id":"rs1432261701","clinical_significance":[],"alleles":["C","T"],"end":140524593,"strand":1,"feature_type":"variation","start":140524593,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524596,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140524596,"clinical_significance":[],"id":"rs1468338047","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795982174","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524597,"feature_type":"variation","strand":1,"end":140524599,"alleles":["AAA","AA"]},{"seq_region_name":"7","id":"rs1795982288","clinical_significance":[],"alleles":["A","G"],"end":140524598,"strand":1,"feature_type":"variation","start":140524598,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs931863515","clinical_significance":[],"end":140524601,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140524601,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140524606,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524606,"clinical_significance":[],"seq_region_name":"7","id":"rs1193811285"},{"seq_region_name":"7","id":"rs374731007","clinical_significance":[],"strand":1,"feature_type":"variation","end":140524611,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524611,"source":"dbSNP"},{"clinical_significance":[],"id":"rs932239193","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140524612,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524612},{"alleles":["C","A","T"],"end":140524614,"strand":1,"feature_type":"variation","start":140524614,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795985849","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1220772385","feature_type":"variation","strand":1,"end":140524616,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524616},{"source":"dbSNP","start":140524618,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140524618,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1365079947"},{"seq_region_name":"7","id":"rs541714601","clinical_significance":[],"strand":1,"feature_type":"variation","end":140524619,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524619,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1353336826","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524625,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140524625},{"id":"rs1795986670","seq_region_name":"7","clinical_significance":[],"start":140524632,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140524632,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"id":"rs1319875365","seq_region_name":"7","clinical_significance":[],"start":140524635,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140524635,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs867369586","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524638,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140524638},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524639,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C","T"],"end":140524639,"id":"rs781500531","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1369286596","seq_region_name":"7","source":"dbSNP","start":140524641,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140524641,"feature_type":"variation","strand":1},{"id":"rs1293277598","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140524649,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524649,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140524652,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524652,"clinical_significance":[],"seq_region_name":"7","id":"rs1795987447"},{"source":"dbSNP","start":140524657,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140524657,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1432154865"},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140524662,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524662,"clinical_significance":[],"seq_region_name":"7","id":"rs1585547584"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795987903","source":"dbSNP","start":140524664,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140524664,"alleles":["C","G","T"],"feature_type":"variation","strand":1},{"end":140524667,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140524667,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs945691522","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1291582754","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524669,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140524669},{"id":"rs1795988457","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524673,"source":"dbSNP","strand":1,"feature_type":"variation","end":140524673,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1417333611","clinical_significance":[],"alleles":["C","T"],"end":140524682,"strand":1,"feature_type":"variation","start":140524682,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1795988626","clinical_significance":[],"alleles":["C","T"],"end":140524686,"strand":1,"feature_type":"variation","start":140524686,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140524690,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140524690,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1379083116"},{"alleles":["C","T"],"end":140524692,"feature_type":"variation","strand":1,"source":"dbSNP","start":140524692,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1173912065"},{"end":140524695,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140524695,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1795989150","seq_region_name":"7"},{"end":140524696,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140524696,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795989297"},{"strand":1,"feature_type":"variation","end":140524698,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524698,"source":"dbSNP","id":"rs1795989460","seq_region_name":"7","clinical_significance":[]},{"id":"rs1795989623","seq_region_name":"7","clinical_significance":[],"start":140524700,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140524700,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs559769549","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524702,"feature_type":"variation","strand":1,"end":140524702,"alleles":["C","A","T"]},{"seq_region_name":"7","id":"rs896523209","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140524703,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524703,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1795990239","seq_region_name":"7","source":"dbSNP","start":140524712,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140524712,"alleles":["G","A"],"feature_type":"variation","strand":1},{"end":140524714,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140524714,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585547672","clinical_significance":[]},{"seq_region_name":"7","id":"rs1795990602","clinical_significance":[],"end":140524719,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140524719,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140524720,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524720,"clinical_significance":[],"seq_region_name":"7","id":"rs555695575"},{"end":140524727,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140524727,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130459519"},{"id":"rs1795990917","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140524729,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524729,"source":"dbSNP"},{"alleles":["C","T"],"end":140524730,"strand":1,"feature_type":"variation","start":140524730,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795991016","clinical_significance":[]},{"end":140524740,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140524740,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795991137","clinical_significance":[]},{"start":140524751,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140524751,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs906967741","clinical_significance":[]},{"id":"rs531868946","seq_region_name":"7","clinical_significance":[],"end":140524760,"alleles":["TTTTTTT","TTTTTTTT"],"strand":1,"feature_type":"variation","start":140524754,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524755,"source":"dbSNP","strand":1,"feature_type":"variation","end":140524755,"alleles":["T","A"],"seq_region_name":"7","id":"rs1795991578","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524756,"source":"dbSNP","strand":1,"feature_type":"variation","end":140524764,"alleles":["TTTTTATAG","-"],"seq_region_name":"7","id":"rs1795991720","clinical_significance":[]},{"id":"rs1307936381","seq_region_name":"7","clinical_significance":[],"alleles":["T","G"],"end":140524759,"strand":1,"feature_type":"variation","start":140524759,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140524760,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524760,"clinical_significance":[],"seq_region_name":"7","id":"rs1002597097"},{"seq_region_name":"7","id":"rs1345948656","clinical_significance":[],"end":140524761,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140524761,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs71520098","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524764,"feature_type":"variation","strand":1,"alleles":["G","-"],"end":140524764},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795992423","source":"dbSNP","start":140524767,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","AA"],"end":140524767,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["ACAA","-"],"end":140524770,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524767,"source":"dbSNP","seq_region_name":"7","id":"rs1563116264","clinical_significance":[]},{"start":140524770,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140524770,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795992702","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140524771,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524771,"source":"dbSNP","seq_region_name":"7","id":"rs770573553","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140524772,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524772,"source":"dbSNP","seq_region_name":"7","id":"rs2130459665","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1034194182","source":"dbSNP","start":140524773,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140524773,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1364450534","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524774,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140524774},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524781,"feature_type":"variation","strand":1,"end":140524781,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1795993366"},{"clinical_significance":[],"id":"rs1287634580","seq_region_name":"7","alleles":["T","A"],"end":140524782,"feature_type":"variation","strand":1,"source":"dbSNP","start":140524782,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140524788,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524788,"source":"dbSNP","id":"rs1795993557","seq_region_name":"7","clinical_significance":[]},{"id":"rs1795993670","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524789,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140524789},{"source":"dbSNP","start":140524790,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140524790,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1399888042","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1359372396","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524794,"source":"dbSNP","strand":1,"feature_type":"variation","end":140524794,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1554458588","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524795,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140524795},{"clinical_significance":[],"seq_region_name":"7","id":"rs548288103","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524800,"feature_type":"variation","strand":1,"alleles":["TTT","TTTT"],"end":140524802},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524804,"feature_type":"variation","strand":1,"end":140524804,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585547849"},{"source":"dbSNP","start":140524812,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140524812,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1795994312","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140524813,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524813,"source":"dbSNP","seq_region_name":"7","id":"rs1795994402","clinical_significance":[]},{"source":"dbSNP","start":140524814,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140524814,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs969887920","seq_region_name":"7"},{"id":"rs1469318292","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140524815,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524815,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs866244790","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524817,"feature_type":"variation","strand":1,"end":140524817,"alleles":["A","T"]},{"alleles":["T","C"],"end":140524819,"strand":1,"feature_type":"variation","start":140524819,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs995455618","clinical_significance":[]},{"alleles":["G","A"],"end":140524820,"strand":1,"feature_type":"variation","start":140524820,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795994948","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140524822,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524822,"clinical_significance":[],"seq_region_name":"7","id":"rs1795995047"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524824,"source":"dbSNP","strand":1,"feature_type":"variation","end":140524824,"alleles":["C","T"],"seq_region_name":"7","id":"rs1795995139","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524827,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140524827,"clinical_significance":[],"seq_region_name":"7","id":"rs1488343508"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140524828,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524828,"clinical_significance":[],"seq_region_name":"7","id":"rs1421306753"},{"feature_type":"variation","strand":1,"alleles":["GCCTCAGCCTC","GCCTCAGCCTCAGCCTC"],"end":140524839,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524829,"clinical_significance":[],"id":"rs1795995447","seq_region_name":"7"},{"seq_region_name":"7","id":"rs148346324","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524830,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140524830},{"end":140524831,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140524831,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1795995674"},{"seq_region_name":"7","id":"rs540852102","clinical_significance":[],"strand":1,"feature_type":"variation","end":140524836,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524836,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140524839,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524839,"clinical_significance":[],"seq_region_name":"7","id":"rs1252214429"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795995987","feature_type":"variation","strand":1,"end":140524841,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524841},{"clinical_significance":[],"seq_region_name":"7","id":"rs1258362097","source":"dbSNP","start":140524845,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140524845,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524848,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140524848,"seq_region_name":"7","id":"rs1795996319","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1795996409","end":140524849,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140524849,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140524856,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C","T"],"end":140524856,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs6965362","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140524857,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524857,"clinical_significance":[],"id":"rs1157779147","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1795996591","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524857,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","TT"],"end":140524857},{"seq_region_name":"7","id":"rs1417875718","clinical_significance":[],"end":140524860,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140524860,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs79752651","clinical_significance":[],"alleles":["T","C"],"end":140524861,"strand":1,"feature_type":"variation","start":140524861,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["CCCC","CCC"],"end":140524868,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524865,"clinical_significance":[],"seq_region_name":"7","id":"rs1795996817"},{"start":140524868,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140524868,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs545010819","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524869,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140524869,"seq_region_name":"7","id":"rs1795997012","clinical_significance":[]},{"alleles":["G","A"],"end":140524870,"strand":1,"feature_type":"variation","start":140524870,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs966533290","clinical_significance":[]},{"start":140524873,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140524873,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585548057","clinical_significance":[]},{"seq_region_name":"7","id":"rs976097797","clinical_significance":[],"alleles":["G","A"],"end":140524874,"strand":1,"feature_type":"variation","start":140524874,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs563297184","source":"dbSNP","start":140524875,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140524875,"alleles":["G","A","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585548080","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524876,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140524876},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524880,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140524880,"seq_region_name":"7","id":"rs1293447719","clinical_significance":[]},{"alleles":["A","T"],"end":140524882,"strand":1,"feature_type":"variation","start":140524882,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1585548099","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1416078521","source":"dbSNP","start":140524883,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140524883,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524883,"source":"dbSNP","strand":1,"feature_type":"variation","end":140524888,"alleles":["TTCTTT","TT"],"id":"rs1795997951","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs144664901","seq_region_name":"7","source":"dbSNP","start":140524885,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","-"],"end":140524885,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs200448743","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524885,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140524885},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524886,"feature_type":"variation","strand":1,"end":140524903,"alleles":["TTTTTTTTTTTTTTTTTT","TTTTTTTTT","TTTTTTTTTT","TTTTTTTTTTT","TTTTTTTTTTTT","TTTTTTTTTTTTT","TTTTTTTTTTTTTT","TTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTT"],"clinical_significance":[],"seq_region_name":"7","id":"rs773550888"},{"alleles":["-","C"],"end":140524886,"strand":1,"feature_type":"variation","start":140524887,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1795998783","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140524887,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140524887,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs921586511"},{"start":140524888,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140524887,"alleles":["-","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1795998973","clinical_significance":[]},{"alleles":["TTTT","TTTTTGTTTT"],"end":140524903,"strand":1,"feature_type":"variation","start":140524900,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1795999106","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140524901,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524901,"clinical_significance":[],"id":"rs1795999217","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1198407305","clinical_significance":[],"strand":1,"feature_type":"variation","end":140524903,"alleles":["T","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524903,"source":"dbSNP"},{"id":"rs1795999517","seq_region_name":"7","clinical_significance":[],"end":140524904,"alleles":["TG","-"],"strand":1,"feature_type":"variation","start":140524903,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1336186823","alleles":["G","-"],"end":140524904,"feature_type":"variation","strand":1,"source":"dbSNP","start":140524904,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524904,"feature_type":"variation","strand":1,"end":140524904,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1442629468"},{"clinical_significance":[],"id":"rs756947972","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["GAAACGGAGTCTCGCTCTGTCGCCCAGGTT","AACTG"],"end":140524933,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524904},{"feature_type":"variation","strand":1,"end":140524905,"alleles":["A","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524905,"clinical_significance":[],"id":"rs1299014811","seq_region_name":"7"},{"source":"dbSNP","start":140524906,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140524906,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585548242"},{"id":"rs567251255","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140524908,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524908,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140524909,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524909,"clinical_significance":[],"id":"rs1338225587","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585548265","end":140524911,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140524911,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140524912,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524912,"clinical_significance":[],"seq_region_name":"7","id":"rs1796000498"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524913,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140524913,"seq_region_name":"7","id":"rs1585548272","clinical_significance":[]},{"id":"rs1311330492","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140524916,"strand":1,"feature_type":"variation","start":140524916,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1352555044","feature_type":"variation","strand":1,"end":140524917,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524917},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140524918,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524918,"source":"dbSNP","seq_region_name":"7","id":"rs1796000872","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140524919,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524919,"source":"dbSNP","id":"rs1408158312","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140524924,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524924,"clinical_significance":[],"seq_region_name":"7","id":"rs1329114075"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140524925,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524925,"source":"dbSNP","seq_region_name":"7","id":"rs1464916990","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs931726606","alleles":["C","T"],"end":140524927,"feature_type":"variation","strand":1,"source":"dbSNP","start":140524927,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140524930,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524930,"source":"dbSNP","id":"rs1167050816","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585548323","source":"dbSNP","start":140524932,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140524932,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524935,"source":"dbSNP","strand":1,"feature_type":"variation","end":140524935,"alleles":["G","C"],"seq_region_name":"7","id":"rs1287836798","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585548340","clinical_significance":[],"end":140524936,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","start":140524936,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140524937,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140524937,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1796001793","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140524946,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524946,"source":"dbSNP","seq_region_name":"7","id":"rs1456282576","clinical_significance":[]},{"start":140524947,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C"],"end":140524947,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs141501845","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140524948,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524948,"clinical_significance":[],"seq_region_name":"7","id":"rs1796002166"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796002261","alleles":["G","A"],"end":140524949,"feature_type":"variation","strand":1,"source":"dbSNP","start":140524949,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140524954,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G","T"],"end":140524954,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs113664505","clinical_significance":[]},{"start":140524955,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140524955,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","id":"rs1288327522","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140524956,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524956,"clinical_significance":[],"seq_region_name":"7","id":"rs1796002670"},{"strand":1,"feature_type":"variation","end":140524957,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524957,"source":"dbSNP","seq_region_name":"7","id":"rs774961379","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130460464","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524958,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140524958},{"id":"rs147515269","seq_region_name":"7","clinical_significance":[],"start":140524959,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140524959,"strand":1,"feature_type":"variation"},{"alleles":["T","C"],"end":140524961,"feature_type":"variation","strand":1,"source":"dbSNP","start":140524961,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1796003020","seq_region_name":"7"},{"source":"dbSNP","start":140524969,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140524969,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796003135"},{"seq_region_name":"7","id":"rs1796003235","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524970,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140524970},{"seq_region_name":"7","id":"rs1469194517","clinical_significance":[],"start":140524971,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140524971,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585548430","source":"dbSNP","start":140524972,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140524972,"alleles":["A","C","G"],"feature_type":"variation","strand":1},{"alleles":["C","A","T"],"end":140524973,"feature_type":"variation","strand":1,"source":"dbSNP","start":140524973,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs561233759"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796003713","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524975,"feature_type":"variation","strand":1,"end":140524975,"alleles":["T","C"]},{"start":140524986,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140524985,"alleles":["-","AG"],"strand":1,"feature_type":"variation","id":"rs1205657093","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524986,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140524986,"clinical_significance":[],"seq_region_name":"7","id":"rs1255244821"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1356238727","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524987,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140524987},{"feature_type":"variation","strand":1,"end":140524988,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524988,"clinical_significance":[],"id":"rs1796004142","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1254340734","clinical_significance":[],"start":140524988,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140524989,"alleles":["CT","-"],"strand":1,"feature_type":"variation"},{"id":"rs1208606434","seq_region_name":"7","clinical_significance":[],"start":140524988,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["CTATTC","CTATTCCTATTC"],"end":140524993,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1264397618","feature_type":"variation","strand":1,"alleles":["T","A"],"end":140524989,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140524989},{"seq_region_name":"7","id":"rs1481875546","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524990,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140524990},{"seq_region_name":"7","id":"rs1796004699","clinical_significance":[],"strand":1,"feature_type":"variation","end":140524996,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140524996,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1180942659","seq_region_name":"7","source":"dbSNP","start":140524999,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140524999,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1257640535","source":"dbSNP","start":140525002,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140525002,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140525003,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525003,"clinical_significance":[],"seq_region_name":"7","id":"rs1585548523"},{"seq_region_name":"7","id":"rs922144084","clinical_significance":[],"start":140525009,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140525009,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140525012,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525012,"source":"dbSNP","id":"rs1796005200","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs762828867","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525013,"feature_type":"variation","strand":1,"end":140525013,"alleles":["G","A","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796005468","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140525014,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525014},{"alleles":["T","C"],"end":140525018,"strand":1,"feature_type":"variation","start":140525018,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs935148710","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1410387229","source":"dbSNP","start":140525022,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140525022,"alleles":["A","C"],"feature_type":"variation","strand":1},{"start":140525023,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140525023,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1172273711","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525029,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140525029,"seq_region_name":"7","id":"rs749325894","clinical_significance":[]},{"id":"rs1371485697","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525030,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140525030},{"strand":1,"feature_type":"variation","alleles":["CGTAAA","-"],"end":140525035,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525030,"source":"dbSNP","id":"rs1428101392","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525031,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140525031,"clinical_significance":[],"seq_region_name":"7","id":"rs1052373722"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525032,"feature_type":"variation","strand":1,"end":140525032,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1385047665"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525036,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140525036,"clinical_significance":[],"seq_region_name":"7","id":"rs1389918562"},{"strand":1,"feature_type":"variation","end":140525042,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525042,"source":"dbSNP","seq_region_name":"7","id":"rs1796007014","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796007117","feature_type":"variation","strand":1,"end":140525044,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525044},{"start":140525045,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140525045,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1356235764","clinical_significance":[]},{"start":140525047,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140525047,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs528715664","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140525048,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525048,"source":"dbSNP","seq_region_name":"7","id":"rs990391370","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140525049,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525049,"source":"dbSNP","seq_region_name":"7","id":"rs1158307661","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796007631","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140525051,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525051},{"seq_region_name":"7","id":"rs531482099","clinical_significance":[],"alleles":["G","T"],"end":140525052,"strand":1,"feature_type":"variation","start":140525052,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1176382687","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140525053,"strand":1,"feature_type":"variation","start":140525053,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["CATGGTGGTGCATGCC","C"],"end":140525068,"feature_type":"variation","strand":1,"source":"dbSNP","start":140525053,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1397330310"},{"seq_region_name":"7","id":"rs1197166709","clinical_significance":[],"alleles":["G","A"],"end":140525059,"strand":1,"feature_type":"variation","start":140525059,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs946299080","seq_region_name":"7","clinical_significance":[],"start":140525060,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140525060,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796008209","end":140525061,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140525061,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525063,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140525063,"seq_region_name":"7","id":"rs1041792051","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525065,"feature_type":"variation","strand":1,"end":140525065,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs140143130"},{"seq_region_name":"7","id":"rs938449368","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140525066,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525066,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1796008646","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140525069,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525069,"source":"dbSNP"},{"end":140525077,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140525077,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796008729","clinical_significance":[]},{"end":140525081,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140525081,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1215612410"},{"strand":1,"feature_type":"variation","end":140525085,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525085,"source":"dbSNP","seq_region_name":"7","id":"rs905155151","clinical_significance":[]},{"alleles":["G","A"],"end":140525088,"strand":1,"feature_type":"variation","start":140525088,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796009016","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1283214264","end":140525098,"alleles":["AGGTGGGAAG","AGGTGGGAAGGTGGGAAG"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140525089,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1277236602","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525094,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140525094},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140525095,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525095,"clinical_significance":[],"seq_region_name":"7","id":"rs1340428806"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1239031784","end":140525103,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140525103,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525106,"source":"dbSNP","strand":1,"feature_type":"variation","end":140525106,"alleles":["G","A"],"seq_region_name":"7","id":"rs1796009518","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796009620","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525109,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140525109},{"end":140525112,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140525112,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1204051753","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585548771","clinical_significance":[],"start":140525115,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140525115,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525122,"source":"dbSNP","strand":1,"feature_type":"variation","end":140525122,"alleles":["G","T"],"seq_region_name":"7","id":"rs1796009948","clinical_significance":[]},{"id":"rs1055543282","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525124,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140525124},{"seq_region_name":"7","id":"rs181703538","clinical_significance":[],"start":140525125,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140525125,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs549604410","alleles":["G","A","C","T"],"end":140525126,"feature_type":"variation","strand":1,"source":"dbSNP","start":140525126,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140525137,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525137,"source":"dbSNP","seq_region_name":"7","id":"rs1796010403","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796010483","source":"dbSNP","start":140525139,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140525139,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140525144,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525144,"clinical_significance":[],"seq_region_name":"7","id":"rs1585548819"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525146,"feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140525146,"clinical_significance":[],"seq_region_name":"7","id":"rs1207404365"},{"seq_region_name":"7","id":"rs1796010803","clinical_significance":[],"strand":1,"feature_type":"variation","end":140525147,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525147,"source":"dbSNP"},{"source":"dbSNP","start":140525148,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140525148,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1330228997"},{"seq_region_name":"7","id":"rs1796011038","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525150,"source":"dbSNP","strand":1,"feature_type":"variation","end":140525150,"alleles":["T","A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585548852","end":140525151,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140525151,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1796011230","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140525152,"alleles":["T","TT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525152,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140525153,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525153,"clinical_significance":[],"seq_region_name":"7","id":"rs868583052"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796011463","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525154,"feature_type":"variation","strand":1,"end":140525154,"alleles":["T","C","G"]},{"feature_type":"variation","strand":1,"end":140525171,"alleles":["TTTTTTTTTTTTTTTTTT","TTTTTTTTTTTT","TTTTTTTTTTTTT","TTTTTTTTTTTTTT","TTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525154,"clinical_significance":[],"seq_region_name":"7","id":"rs1198329788"},{"start":140525160,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140525160,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1377484670","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","TCT"],"end":140525166,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525166,"source":"dbSNP","seq_region_name":"7","id":"rs1170974613","clinical_significance":[]},{"end":140525170,"alleles":["-","C"],"strand":1,"feature_type":"variation","start":140525171,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1475706859","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796012349","clinical_significance":[],"end":140525171,"alleles":["T","TTCT"],"strand":1,"feature_type":"variation","start":140525171,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["-","TTTTG"],"end":140525171,"strand":1,"feature_type":"variation","start":140525172,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796012464","clinical_significance":[]},{"source":"dbSNP","start":140525172,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140525172,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1200251899","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796012676","feature_type":"variation","strand":1,"end":140525173,"alleles":["GG","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525172},{"clinical_significance":[],"seq_region_name":"7","id":"rs1448624062","source":"dbSNP","start":140525174,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140525174,"alleles":["A","C","G","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1796012929","clinical_significance":[],"end":140525174,"alleles":["A","-"],"strand":1,"feature_type":"variation","start":140525174,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796013039","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525175,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140525175},{"clinical_significance":[],"id":"rs1585548959","seq_region_name":"7","end":140525176,"alleles":["A","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140525176,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140525177,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525177,"clinical_significance":[],"seq_region_name":"7","id":"rs1585548970"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1168264745","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525178,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140525178},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525180,"source":"dbSNP","strand":1,"feature_type":"variation","end":140525180,"alleles":["G","T"],"seq_region_name":"7","id":"rs1796013496","clinical_significance":[]},{"clinical_significance":[],"id":"rs571431501","seq_region_name":"7","source":"dbSNP","start":140525181,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140525181,"alleles":["A","C","G","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1796013773","clinical_significance":[],"end":140525190,"alleles":["TCTCACTCT","TCT"],"strand":1,"feature_type":"variation","start":140525182,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1371162803","seq_region_name":"7","alleles":["A","C","G","T"],"end":140525186,"feature_type":"variation","strand":1,"source":"dbSNP","start":140525186,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796014054","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525187,"feature_type":"variation","strand":1,"end":140525190,"alleles":["CTCT","CT"]},{"feature_type":"variation","strand":1,"end":140525191,"alleles":["G","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525191,"clinical_significance":[],"seq_region_name":"7","id":"rs1027021089"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1416318331","end":140525194,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140525194,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140525196,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140525196,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1796014432","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1344060118","alleles":["C","T"],"end":140525201,"feature_type":"variation","strand":1,"source":"dbSNP","start":140525201,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525202,"source":"dbSNP","strand":1,"feature_type":"variation","end":140525202,"alleles":["T","A","C"],"seq_region_name":"7","id":"rs951589935","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140525204,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525204,"clinical_significance":[],"seq_region_name":"7","id":"rs1796014825"},{"source":"dbSNP","start":140525205,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140525205,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796014905"},{"id":"rs1220434126","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525206,"source":"dbSNP","strand":1,"feature_type":"variation","end":140525206,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1796015291","clinical_significance":[],"alleles":["G","T"],"end":140525211,"strand":1,"feature_type":"variation","start":140525211,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140525212,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525212,"source":"dbSNP","seq_region_name":"7","id":"rs2130461397","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525213,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140525213,"clinical_significance":[],"seq_region_name":"7","id":"rs1796015385"},{"seq_region_name":"7","id":"rs187122190","clinical_significance":[],"end":140525215,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140525215,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1277706898","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525216,"source":"dbSNP","strand":1,"feature_type":"variation","end":140525216,"alleles":["G","A"]},{"clinical_significance":[],"id":"rs2130461427","seq_region_name":"7","source":"dbSNP","start":140525217,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140525217,"alleles":["C","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1796015678","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140525219,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525219},{"seq_region_name":"7","id":"rs1019895034","clinical_significance":[],"alleles":["T","A"],"end":140525222,"strand":1,"feature_type":"variation","start":140525222,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["C","G","T"],"end":140525223,"strand":1,"feature_type":"variation","start":140525223,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585549072","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525224,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140525224,"seq_region_name":"7","id":"rs1796015964","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1377298375","feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140525225,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525225},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796016192","alleles":["C","T"],"end":140525226,"feature_type":"variation","strand":1,"source":"dbSNP","start":140525226,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1796016296","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140525232,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525232,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1796016386","clinical_significance":[],"start":140525236,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140525236,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1332469914","feature_type":"variation","strand":1,"end":140525237,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525237},{"clinical_significance":[],"seq_region_name":"7","id":"rs34177311","end":140525240,"alleles":["CC","CCC"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140525239,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525240,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140525240,"clinical_significance":[],"seq_region_name":"7","id":"rs1796016657"},{"end":140525241,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140525241,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs2130461547","seq_region_name":"7","clinical_significance":[]},{"id":"rs1585549113","seq_region_name":"7","clinical_significance":[],"end":140525244,"alleles":["ACCT","ACCTACCT"],"strand":1,"feature_type":"variation","start":140525241,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1414084786","seq_region_name":"7","source":"dbSNP","start":140525242,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140525242,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525246,"source":"dbSNP","strand":1,"feature_type":"variation","end":140525246,"alleles":["C","T"],"seq_region_name":"7","id":"rs1397712007","clinical_significance":[]},{"end":140525250,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140525250,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1169986984","clinical_significance":[]},{"clinical_significance":[],"id":"rs1464574053","seq_region_name":"7","source":"dbSNP","start":140525252,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140525252,"alleles":["T","C"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525254,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140525254,"seq_region_name":"7","id":"rs1048202657","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525255,"feature_type":"variation","strand":1,"end":140525255,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs966028123"},{"end":140525258,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140525258,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1796017376","seq_region_name":"7"},{"alleles":["C","G"],"end":140525262,"feature_type":"variation","strand":1,"source":"dbSNP","start":140525262,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1796017604","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1358597500","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525262,"source":"dbSNP","strand":1,"feature_type":"variation","end":140525266,"alleles":["CTCCT","CT"]},{"feature_type":"variation","strand":1,"end":140525264,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525264,"clinical_significance":[],"seq_region_name":"7","id":"rs1796017824"},{"seq_region_name":"7","id":"rs373327171","clinical_significance":[],"start":140525265,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140525270,"alleles":["CTGTCT","CT"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140525266,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140525266,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796018039"},{"seq_region_name":"7","id":"rs1796018130","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525268,"source":"dbSNP","strand":1,"feature_type":"variation","end":140525268,"alleles":["T","C"]},{"start":140525271,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140525271,"strand":1,"feature_type":"variation","id":"rs921601872","seq_region_name":"7","clinical_significance":[]},{"id":"rs1796018448","seq_region_name":"7","clinical_significance":[],"end":140525277,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140525277,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525281,"feature_type":"variation","strand":1,"alleles":["A","C","T"],"end":140525281,"clinical_significance":[],"seq_region_name":"7","id":"rs2130461688"},{"clinical_significance":[],"id":"rs1796018591","seq_region_name":"7","source":"dbSNP","start":140525286,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140525286,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525287,"source":"dbSNP","strand":1,"feature_type":"variation","end":140525287,"alleles":["T","-"],"seq_region_name":"7","id":"rs1796018723","clinical_significance":[]},{"clinical_significance":[],"id":"rs953065357","seq_region_name":"7","end":140525297,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140525297,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140525300,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525300,"source":"dbSNP","seq_region_name":"7","id":"rs1796019020","clinical_significance":[]},{"clinical_significance":[],"id":"rs1796019155","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525305,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140525305},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525308,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140525308,"clinical_significance":[],"seq_region_name":"7","id":"rs1796019283"},{"clinical_significance":[],"id":"rs1441447985","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140525311,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525311},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525312,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140525312,"seq_region_name":"7","id":"rs1796019551","clinical_significance":[]},{"seq_region_name":"7","id":"rs979213605","clinical_significance":[],"start":140525314,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140525314,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"alleles":["A","G"],"end":140525320,"feature_type":"variation","strand":1,"source":"dbSNP","start":140525320,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796019839"},{"end":140525322,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140525322,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1200286022","seq_region_name":"7","clinical_significance":[]},{"end":140525326,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140525326,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796020081","clinical_significance":[]},{"source":"dbSNP","start":140525330,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140525330,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1303773885","seq_region_name":"7"},{"alleles":["A","G"],"end":140525336,"strand":1,"feature_type":"variation","start":140525336,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1316058119","clinical_significance":[]},{"start":140525344,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["GGGG","GGGGG"],"end":140525347,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1257366649","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140525345,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525345,"source":"dbSNP","id":"rs2130461811","seq_region_name":"7","clinical_significance":[]},{"start":140525346,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140525346,"alleles":["G","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs539680762","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525349,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140525349,"seq_region_name":"7","id":"rs551398070","clinical_significance":[]},{"id":"rs1381475734","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525353,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140525353},{"seq_region_name":"7","id":"rs887038261","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525355,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140525355},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525361,"feature_type":"variation","strand":1,"end":140525361,"alleles":["G","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs760705917"},{"feature_type":"variation","strand":1,"alleles":["G","A","C","T"],"end":140525366,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525366,"clinical_significance":[],"seq_region_name":"7","id":"rs1004098628"},{"seq_region_name":"7","id":"rs865854860","clinical_significance":[],"start":140525374,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140525374,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140525375,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140525375,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs569713066"},{"clinical_significance":[],"id":"rs1796021456","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140525378,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525378},{"seq_region_name":"7","id":"rs1796021551","clinical_significance":[],"start":140525381,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140525381,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"end":140525382,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140525382,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1333867577","clinical_significance":[]},{"clinical_significance":[],"id":"rs1445032414","seq_region_name":"7","source":"dbSNP","start":140525385,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140525385,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796021950","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525388,"feature_type":"variation","strand":1,"end":140525388,"alleles":["C","G","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs191894644","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525391,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140525391},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796022177","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525392,"feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140525392},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140525399,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525399,"source":"dbSNP","seq_region_name":"7","id":"rs1796022251","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796022324","feature_type":"variation","strand":1,"end":140525403,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525403},{"end":140525406,"alleles":["TCTC","TC"],"strand":1,"feature_type":"variation","start":140525403,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1166312128","clinical_significance":[]},{"end":140525407,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140525407,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796022496"},{"start":140525408,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140525408,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796022585","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525409,"source":"dbSNP","strand":1,"feature_type":"variation","end":140525409,"alleles":["C","G"],"id":"rs1796022665","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1463436235","source":"dbSNP","start":140525417,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140525417,"alleles":["A","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1415378315","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525420,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140525420},{"end":140525426,"alleles":["A","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140525426,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796022959"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796023053","alleles":["T","C"],"end":140525428,"feature_type":"variation","strand":1,"source":"dbSNP","start":140525428,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140525430,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525430,"source":"dbSNP","seq_region_name":"7","id":"rs1447049838","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525434,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140525434,"id":"rs1029021800","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs953571566","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140525437,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525437,"source":"dbSNP"},{"id":"rs555732535","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140525440,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525440,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1246105207","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525448,"feature_type":"variation","strand":1,"end":140525448,"alleles":["C","A","T"]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140525451,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525451,"clinical_significance":[],"id":"rs1796023717","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1796023806","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525452,"source":"dbSNP","strand":1,"feature_type":"variation","end":140525452,"alleles":["G","A","C"]},{"alleles":["C","A"],"end":140525453,"feature_type":"variation","strand":1,"source":"dbSNP","start":140525453,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796023909"},{"start":140525455,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140525455,"strand":1,"feature_type":"variation","id":"rs1180066028","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1052278284","end":140525461,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140525461,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1563116679","clinical_significance":[],"start":140525461,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AAAAA","AAAA","AAAAAA"],"end":140525465,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["AAAAA","AAAAAA"],"end":140525472,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525468,"source":"dbSNP","seq_region_name":"7","id":"rs1796024296","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525472,"feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140525472,"clinical_significance":[],"id":"rs990744509","seq_region_name":"7"},{"start":140525475,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140525492,"alleles":["TAGGTGCCTATAGTTATA","TAGGTGCCTATAGTTATATAGGTGCCTATAGTTATA"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796024507","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525477,"feature_type":"variation","strand":1,"end":140525477,"alleles":["G","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs144109674"},{"end":140525478,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140525478,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs968044120","clinical_significance":[]},{"seq_region_name":"7","id":"rs1227805705","clinical_significance":[],"alleles":["G","-"],"end":140525480,"strand":1,"feature_type":"variation","start":140525480,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140525481,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525481,"clinical_significance":[],"seq_region_name":"7","id":"rs1351408395"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1044957670","end":140525483,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140525483,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs905227941","source":"dbSNP","start":140525487,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140525487,"alleles":["G","A","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1439278365","feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140525488,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525488},{"seq_region_name":"7","id":"rs375477113","clinical_significance":[],"end":140525491,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140525491,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525493,"source":"dbSNP","strand":1,"feature_type":"variation","end":140525493,"alleles":["A","C","G"],"seq_region_name":"7","id":"rs977664617","clinical_significance":[]},{"start":140525497,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140525497,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130462289","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140525498,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525498,"clinical_significance":[],"seq_region_name":"7","id":"rs1796025500"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525501,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140525501,"seq_region_name":"7","id":"rs995465979","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs764158132","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525503,"feature_type":"variation","strand":1,"end":140525503,"alleles":["G","A","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525505,"feature_type":"variation","strand":1,"end":140525505,"alleles":["A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs9718814"},{"source":"dbSNP","start":140525508,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TTTTT","TTTTTT"],"end":140525512,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796025911"},{"clinical_significance":[],"id":"rs1055574213","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525510,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140525510},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140525511,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525511,"clinical_significance":[],"seq_region_name":"7","id":"rs2130462385"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525517,"source":"dbSNP","strand":1,"feature_type":"variation","end":140525517,"alleles":["T","C"],"seq_region_name":"7","id":"rs1160121747","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs73163296","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525526,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140525526},{"id":"rs1379511780","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140525529,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525529,"source":"dbSNP"},{"seq_region_name":"7","id":"rs2130462423","clinical_significance":[],"start":140525531,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140525531,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525537,"feature_type":"variation","strand":1,"end":140525537,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs764912553"},{"end":140525542,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140525542,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1343754453"},{"seq_region_name":"7","id":"rs1194017361","clinical_significance":[],"start":140525543,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140525543,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140525546,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140525546,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1489462813"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525547,"source":"dbSNP","strand":1,"feature_type":"variation","end":140525547,"alleles":["G","A"],"seq_region_name":"7","id":"rs1244915515","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525559,"feature_type":"variation","strand":1,"end":140525559,"alleles":["C","G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1220666104"},{"id":"rs1424597362","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140525560,"strand":1,"feature_type":"variation","start":140525560,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["T","G"],"end":140525561,"strand":1,"feature_type":"variation","start":140525561,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1447677764","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796027148","alleles":["A","G"],"end":140525568,"feature_type":"variation","strand":1,"source":"dbSNP","start":140525568,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140525572,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140525572,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585549704","clinical_significance":[]},{"alleles":["C","T"],"end":140525573,"strand":1,"feature_type":"variation","start":140525573,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1585549710","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140525577,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525577,"source":"dbSNP","seq_region_name":"7","id":"rs1457815782","clinical_significance":[]},{"alleles":["T","C"],"end":140525579,"strand":1,"feature_type":"variation","start":140525579,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1323207700","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796027625","source":"dbSNP","start":140525585,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140525585,"feature_type":"variation","strand":1},{"id":"rs931021053","seq_region_name":"7","clinical_significance":[],"start":140525587,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140525587,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140525591,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140525591,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1353227386"},{"start":140525595,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140525595,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796027911","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140525598,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525598,"clinical_significance":[],"seq_region_name":"7","id":"rs1796028010"},{"feature_type":"variation","strand":1,"end":140525600,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525600,"clinical_significance":[],"seq_region_name":"7","id":"rs1304698641"},{"clinical_significance":[],"id":"rs1221287764","seq_region_name":"7","alleles":["C","T"],"end":140525605,"feature_type":"variation","strand":1,"source":"dbSNP","start":140525605,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525607,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CAGCCCAGCCC","CAGCCC"],"end":140525617,"id":"rs768420523","seq_region_name":"7","clinical_significance":[]},{"end":140525618,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140525618,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1048711444"},{"strand":1,"feature_type":"variation","end":140525619,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525619,"source":"dbSNP","seq_region_name":"7","id":"rs1432065938","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796028653","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140525621,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525621,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1434921257","clinical_significance":[],"start":140525627,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140525627,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1585549803","clinical_significance":[],"end":140525628,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140525628,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525629,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140525629,"clinical_significance":[],"seq_region_name":"7","id":"rs1360655710"},{"start":140525634,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140525634,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1299477382","clinical_significance":[]},{"id":"rs1327008370","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140525640,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525640,"source":"dbSNP"},{"end":140525641,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140525641,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1333138498","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs901307421","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525642,"feature_type":"variation","strand":1,"end":140525642,"alleles":["C","T"]},{"end":140525644,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140525644,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs886905963"},{"end":140525656,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140525656,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1796029465","seq_region_name":"7"},{"source":"dbSNP","start":140525667,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140525667,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796029557"},{"id":"rs1585549867","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C","T"],"end":140525677,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525677,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525679,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140525679,"seq_region_name":"7","id":"rs1796029783","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796029863","clinical_significance":[],"end":140525683,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140525683,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["G","T"],"end":140525690,"strand":1,"feature_type":"variation","start":140525690,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1434700476","seq_region_name":"7","clinical_significance":[]},{"id":"rs1230662356","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140525696,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525696,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1194373514","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525703,"source":"dbSNP","strand":1,"feature_type":"variation","end":140525703,"alleles":["A","C","G"]},{"seq_region_name":"7","id":"rs780708233","clinical_significance":[],"strand":1,"feature_type":"variation","end":140525705,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525705,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525706,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140525706,"clinical_significance":[],"id":"rs1796030363","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1004576381","clinical_significance":[],"alleles":["T","C"],"end":140525709,"strand":1,"feature_type":"variation","start":140525709,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525713,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140525713,"seq_region_name":"7","id":"rs1796030569","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140525715,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525715,"source":"dbSNP","seq_region_name":"7","id":"rs1474736761","clinical_significance":[]},{"seq_region_name":"7","id":"rs1165630416","clinical_significance":[],"start":140525722,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140525722,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"end":140525725,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140525725,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796030835"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525727,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140525727,"id":"rs1413491240","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","C"],"end":140525728,"strand":1,"feature_type":"variation","start":140525728,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130462819","clinical_significance":[]},{"start":140525729,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["GGCCGTCGCTGGCC","GGCC"],"end":140525742,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585549957","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1389082459","source":"dbSNP","start":140525731,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140525731,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs200901456","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525732,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140525732},{"feature_type":"variation","strand":1,"end":140525733,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525733,"clinical_significance":[],"seq_region_name":"7","id":"rs372832400"},{"id":"rs779193196","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140525735,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525735,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140525736,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525736,"source":"dbSNP","seq_region_name":"7","id":"rs748370133","clinical_significance":[]},{"clinical_significance":[],"id":"rs1318768021","seq_region_name":"7","source":"dbSNP","start":140525737,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140525737,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140525740,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525740,"clinical_significance":[],"seq_region_name":"7","id":"rs1328103400"},{"end":140525741,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140525741,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs7781255"},{"seq_region_name":"7","id":"rs2130462925","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525742,"source":"dbSNP","strand":1,"feature_type":"variation","end":140525742,"alleles":["C","T"]},{"start":140525745,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_donor_region_variant","end":140525745,"alleles":["A","C"],"strand":1,"feature_type":"variation","id":"rs1585550036","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1281306224","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140525746,"consequence_type":"splice_donor_5th_base_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525746},{"feature_type":"variation","strand":1,"end":140525748,"alleles":["C","G","T"],"consequence_type":"splice_donor_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525748,"clinical_significance":[],"seq_region_name":"7","id":"rs777780915"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140525750,"consequence_type":"splice_donor_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525750,"clinical_significance":[],"seq_region_name":"7","id":"rs1796032718"},{"seq_region_name":"7","id":"rs1796032783","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140525757,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140525757},{"id":"rs369932936","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140525760,"strand":1,"feature_type":"variation","start":140525760,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs769653009","end":140525761,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140525761,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140525763,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525763,"clinical_significance":[],"seq_region_name":"7","id":"rs557027807"},{"clinical_significance":["uncertain significance"],"seq_region_name":"7","id":"rs749243995","alleles":["C","T"],"end":140525764,"feature_type":"variation","strand":1,"source":"dbSNP","start":140525764,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525765,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140525765,"clinical_significance":["uncertain significance"],"id":"rs373105289","seq_region_name":"7"},{"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525766,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140525766,"clinical_significance":[],"seq_region_name":"7","id":"rs774056832"},{"seq_region_name":"7","id":"rs1796033373","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140525768,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140525768,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs761490205","feature_type":"variation","strand":1,"end":140525770,"alleles":["T","G"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525770},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140525774,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140525774,"seq_region_name":"7","id":"rs201986896","clinical_significance":["uncertain significance"]},{"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525775,"feature_type":"variation","strand":1,"end":140525775,"alleles":["G","A"],"clinical_significance":[],"id":"rs772777594","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1454290650","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140525777,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525777},{"strand":1,"feature_type":"variation","end":140525778,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140525778,"source":"dbSNP","seq_region_name":"7","id":"rs61737086","clinical_significance":[]},{"clinical_significance":[],"id":"rs1585550198","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140525779,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525779},{"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525781,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140525781,"clinical_significance":[],"seq_region_name":"7","id":"rs766042489"},{"source":"dbSNP","start":140525783,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140525783,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs754345800"},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140525784,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525784,"clinical_significance":[],"id":"rs2130463159","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1585550231","clinical_significance":[],"end":140525786,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140525786,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"id":"rs542592596","seq_region_name":"7","clinical_significance":[],"start":140525787,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","end":140525787,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"id":"rs1386948118","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140525788,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140525788},{"alleles":["A","C"],"end":140525791,"strand":1,"feature_type":"variation","start":140525791,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs1796034632","clinical_significance":[]},{"consequence_type":"splice_polypyrimidine_tract_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525801,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140525801,"clinical_significance":[],"seq_region_name":"7","id":"rs561651686"},{"clinical_significance":[],"seq_region_name":"7","id":"rs753025149","consequence_type":"splice_polypyrimidine_tract_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525802,"feature_type":"variation","strand":1,"end":140525802,"alleles":["G","A"]},{"alleles":["C","T"],"end":140525806,"feature_type":"variation","strand":1,"source":"dbSNP","start":140525806,"consequence_type":"splice_polypyrimidine_tract_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs183941457","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"splice_polypyrimidine_tract_variant","start":140525807,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140525807,"seq_region_name":"7","id":"rs1443142602","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525811,"feature_type":"variation","strand":1,"end":140525813,"alleles":["GGG","GG"],"clinical_significance":[],"seq_region_name":"7","id":"rs1261097282"},{"alleles":["G","C"],"end":140525812,"strand":1,"feature_type":"variation","start":140525812,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs777977413","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796035337","clinical_significance":[],"start":140525813,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140525813,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"end":140525816,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140525816,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1330719834"},{"seq_region_name":"7","id":"rs1796035536","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525821,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140525821},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525822,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","-"],"end":140525822,"id":"rs1477542451","seq_region_name":"7","clinical_significance":[]},{"start":140525825,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","T"],"end":140525825,"strand":1,"feature_type":"variation","id":"rs747299398","seq_region_name":"7","clinical_significance":[]},{"end":140525827,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140525827,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs377002476","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525828,"source":"dbSNP","strand":1,"feature_type":"variation","end":140525828,"alleles":["C","G"],"id":"rs1348906159","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs749221164","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525830,"feature_type":"variation","strand":1,"end":140525830,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1274304751","clinical_significance":[],"start":140525832,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140525832,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs768510352","source":"dbSNP","start":140525833,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140525833,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs774150429","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525835,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140525835},{"feature_type":"variation","strand":1,"end":140525837,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525837,"clinical_significance":[],"id":"rs1796036329","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1264721350","feature_type":"variation","strand":1,"end":140525840,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525840},{"end":140525848,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140525848,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796036509","clinical_significance":[]},{"seq_region_name":"7","id":"rs75270012","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525849,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140525849},{"seq_region_name":"7","id":"rs2130463397","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525854,"source":"dbSNP","strand":1,"feature_type":"variation","end":140525854,"alleles":["C","T"]},{"end":140525857,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140525857,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796036699","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525862,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140525862,"seq_region_name":"7","id":"rs565287928","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525866,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140525866,"clinical_significance":[],"seq_region_name":"7","id":"rs1796036873"},{"seq_region_name":"7","id":"rs1585550397","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525867,"source":"dbSNP","strand":1,"feature_type":"variation","end":140525867,"alleles":["C","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1218511408","alleles":["T","C"],"end":140525871,"feature_type":"variation","strand":1,"source":"dbSNP","start":140525871,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140525877,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525877,"source":"dbSNP","seq_region_name":"7","id":"rs1796037132","clinical_significance":[]},{"alleles":["C","T"],"end":140525879,"strand":1,"feature_type":"variation","start":140525879,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1316788081","clinical_significance":[]},{"alleles":["A","G"],"end":140525888,"strand":1,"feature_type":"variation","start":140525888,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796037295","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1164312808","end":140525890,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140525890,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525893,"source":"dbSNP","strand":1,"feature_type":"variation","end":140525893,"alleles":["G","C"],"seq_region_name":"7","id":"rs1585550432","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140525894,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525894,"source":"dbSNP","seq_region_name":"7","id":"rs532748207","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525896,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140525896,"seq_region_name":"7","id":"rs915545753","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs931052062","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525897,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140525897},{"source":"dbSNP","start":140525900,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140525900,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796037911"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585550479","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525901,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140525901},{"source":"dbSNP","start":140525902,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140525902,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs551540587"},{"seq_region_name":"7","id":"rs1585550500","clinical_significance":[],"end":140525905,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140525905,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525906,"feature_type":"variation","strand":1,"end":140525906,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1796038273"},{"feature_type":"variation","strand":1,"end":140525908,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525908,"clinical_significance":[],"seq_region_name":"7","id":"rs1585550514"},{"source":"dbSNP","start":140525909,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140525909,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796038453"},{"seq_region_name":"7","id":"rs1796038527","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525912,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140525912},{"seq_region_name":"7","id":"rs1335986387","clinical_significance":[],"start":140525913,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140525913,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796038709","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525915,"feature_type":"variation","strand":1,"end":140525915,"alleles":["T","C"]},{"source":"dbSNP","start":140525931,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140525931,"alleles":["A","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1447246835"},{"clinical_significance":[],"seq_region_name":"7","id":"rs757826487","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525938,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140525938},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525939,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140525939,"seq_region_name":"7","id":"rs375288420","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1431460170","source":"dbSNP","start":140525940,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140525940,"alleles":["G","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796039227","alleles":["GC","-"],"end":140525944,"feature_type":"variation","strand":1,"source":"dbSNP","start":140525943,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525944,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140525944,"clinical_significance":[],"seq_region_name":"7","id":"rs757181363"},{"seq_region_name":"7","id":"rs2252397","clinical_significance":[],"end":140525950,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140525950,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140525951,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140525951,"alleles":["T","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585550605"},{"seq_region_name":"7","id":"rs1796039697","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525954,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140525954},{"clinical_significance":[],"seq_region_name":"7","id":"rs1041383599","end":140525960,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140525960,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1796039890","seq_region_name":"7","clinical_significance":[],"start":140525963,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140525963,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796039989","feature_type":"variation","strand":1,"end":140525964,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525964},{"seq_region_name":"7","id":"rs1585550637","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525965,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140525965},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796040160","source":"dbSNP","start":140525967,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140525967,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1796040258","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140525969,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525969,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525970,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140525970,"seq_region_name":"7","id":"rs1796040342","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140525971,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525971,"clinical_significance":[],"id":"rs1796040440","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140525973,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525973,"clinical_significance":[],"seq_region_name":"7","id":"rs1585550653"},{"id":"rs1796040634","seq_region_name":"7","clinical_significance":[],"start":140525974,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140525974,"alleles":["G","A","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585550662","alleles":["T","G"],"end":140525976,"feature_type":"variation","strand":1,"source":"dbSNP","start":140525976,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs530547889","seq_region_name":"7","source":"dbSNP","start":140525977,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140525977,"alleles":["C","G"],"feature_type":"variation","strand":1},{"alleles":["C","A"],"end":140525978,"feature_type":"variation","strand":1,"source":"dbSNP","start":140525978,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796040909"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130463794","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140525986,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140525986},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130463804","alleles":["A","G"],"end":140525991,"feature_type":"variation","strand":1,"source":"dbSNP","start":140525991,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525992,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140525992,"id":"rs1796041008","seq_region_name":"7","clinical_significance":[]},{"id":"rs1796041115","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525993,"source":"dbSNP","strand":1,"feature_type":"variation","end":140525993,"alleles":["G","T"]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140525994,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140525994,"source":"dbSNP","id":"rs1166987217","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs149899443","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526003,"feature_type":"variation","strand":1,"end":140526003,"alleles":["C","A","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526004,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140526004,"seq_region_name":"7","id":"rs755468420","clinical_significance":[]},{"seq_region_name":"7","id":"rs1179432707","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526005,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140526005},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140526008,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526008,"clinical_significance":[],"id":"rs1796041651","seq_region_name":"7"},{"alleles":["C","G","T"],"end":140526010,"strand":1,"feature_type":"variation","start":140526010,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1459388023","clinical_significance":[]},{"seq_region_name":"7","id":"rs567561093","clinical_significance":[],"alleles":["G","A"],"end":140526011,"strand":1,"feature_type":"variation","start":140526011,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1469287560","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526014,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140526014},{"end":140526018,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140526018,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796042045"},{"clinical_significance":[],"id":"rs1796042128","seq_region_name":"7","source":"dbSNP","start":140526022,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140526022,"feature_type":"variation","strand":1},{"id":"rs1265576206","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526024,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140526024},{"alleles":["T","C"],"end":140526026,"strand":1,"feature_type":"variation","start":140526026,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs956328041","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526030,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140526030,"clinical_significance":[],"id":"rs1796042462","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140526033,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526033,"clinical_significance":[],"seq_region_name":"7","id":"rs1319330616"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526034,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140526034,"clinical_significance":[],"seq_region_name":"7","id":"rs1354062531"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585550778","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526042,"feature_type":"variation","strand":1,"end":140526042,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs1796043017","clinical_significance":[],"start":140526044,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140526044,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526045,"source":"dbSNP","strand":1,"feature_type":"variation","end":140526045,"alleles":["C","T"],"seq_region_name":"7","id":"rs1585550789","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130463987","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526046,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140526046},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526048,"feature_type":"variation","strand":1,"end":140526048,"alleles":["C","A","T"],"clinical_significance":[],"id":"rs534568200","seq_region_name":"7"},{"seq_region_name":"7","id":"rs988333003","clinical_significance":[],"strand":1,"feature_type":"variation","end":140526049,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526049,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140526053,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526053,"source":"dbSNP","seq_region_name":"7","id":"rs1378892334","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130464027","source":"dbSNP","start":140526057,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140526057,"alleles":["T","C"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526058,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140526058,"clinical_significance":[],"seq_region_name":"7","id":"rs1796043532"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526061,"source":"dbSNP","strand":1,"feature_type":"variation","end":140526061,"alleles":["C","T"],"seq_region_name":"7","id":"rs1796043617","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1329024355","feature_type":"variation","strand":1,"end":140526066,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526066},{"alleles":["T","G"],"end":140526068,"strand":1,"feature_type":"variation","start":140526068,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796043778","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140526073,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526073,"source":"dbSNP","id":"rs546871138","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526075,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","GG"],"end":140526075,"seq_region_name":"7","id":"rs1446024438","clinical_significance":[]},{"alleles":["C","T"],"end":140526078,"strand":1,"feature_type":"variation","start":140526078,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs889078482","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796044329","end":140526080,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140526080,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140526083,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140526083,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1391362980"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526084,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140526084,"seq_region_name":"7","id":"rs1796044513","clinical_significance":[]},{"seq_region_name":"7","id":"rs1024725068","clinical_significance":[],"alleles":["C","G","T"],"end":140526085,"strand":1,"feature_type":"variation","start":140526085,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526086,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140526086,"seq_region_name":"7","id":"rs1184552102","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526088,"source":"dbSNP","strand":1,"feature_type":"variation","end":140526088,"alleles":["T","C"],"seq_region_name":"7","id":"rs571393656","clinical_significance":[]},{"seq_region_name":"7","id":"rs1367917092","clinical_significance":[],"alleles":["G","A"],"end":140526089,"strand":1,"feature_type":"variation","start":140526089,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526099,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140526099,"clinical_significance":[],"seq_region_name":"7","id":"rs1159508959"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526101,"source":"dbSNP","strand":1,"feature_type":"variation","end":140526101,"alleles":["G","A"],"seq_region_name":"7","id":"rs867180941","clinical_significance":[]},{"seq_region_name":"7","id":"rs753934058","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526103,"source":"dbSNP","strand":1,"feature_type":"variation","end":140526103,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1563117135","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526104,"source":"dbSNP","strand":1,"feature_type":"variation","end":140526104,"alleles":["G","C"]},{"seq_region_name":"7","id":"rs1012116258","clinical_significance":[],"strand":1,"feature_type":"variation","end":140526105,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526105,"source":"dbSNP"},{"source":"dbSNP","start":140526109,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140526109,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1441742598"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526113,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140526113,"clinical_significance":[],"seq_region_name":"7","id":"rs1796046057"},{"end":140526114,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140526114,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1796046167","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140526115,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526115,"source":"dbSNP","seq_region_name":"7","id":"rs970992737","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526116,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140526116,"clinical_significance":[],"seq_region_name":"7","id":"rs2130464225"},{"seq_region_name":"7","id":"rs1249753218","clinical_significance":[],"end":140526117,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140526117,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140526124,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526124,"source":"dbSNP","seq_region_name":"7","id":"rs538433018","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1021696886","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140526126,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526126},{"clinical_significance":[],"seq_region_name":"7","id":"rs1452759449","source":"dbSNP","start":140526127,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140526127,"alleles":["G","A"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526129,"source":"dbSNP","strand":1,"feature_type":"variation","end":140526129,"alleles":["T","A"],"seq_region_name":"7","id":"rs1270099808","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1472294040","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526143,"feature_type":"variation","strand":1,"end":140526143,"alleles":["G","A","C"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526144,"source":"dbSNP","strand":1,"feature_type":"variation","end":140526144,"alleles":["C","T"],"seq_region_name":"7","id":"rs867524780","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526147,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CCACCCTAGGGCCCCTGCCTT","CCACCCTAGGGCCCCTGCCTTCCACCCTAGGGCCCCTGCCTT"],"end":140526167,"seq_region_name":"7","id":"rs1796047253","clinical_significance":[]},{"source":"dbSNP","start":140526149,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140526149,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585551029"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526150,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140526150,"id":"rs1290342054","seq_region_name":"7","clinical_significance":[]},{"end":140526154,"alleles":["TA","TATA"],"strand":1,"feature_type":"variation","start":140526153,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1370699042","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796047673","source":"dbSNP","start":140526154,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140526154,"feature_type":"variation","strand":1},{"start":140526155,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140526155,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1456780502","clinical_significance":[]},{"id":"rs34939434","seq_region_name":"7","clinical_significance":[],"alleles":["GGG","GG"],"end":140526157,"strand":1,"feature_type":"variation","start":140526155,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140526158,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140526158,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1796047967","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1306896069","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140526159,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526159,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526168,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","-"],"end":140526168,"seq_region_name":"7","id":"rs1796048175","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526169,"source":"dbSNP","strand":1,"feature_type":"variation","end":140526169,"alleles":["T","A"],"seq_region_name":"7","id":"rs1239167687","clinical_significance":[]},{"start":140526176,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140526176,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1331414988","clinical_significance":[]},{"end":140526177,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140526177,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1796048452","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140526178,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526178,"clinical_significance":[],"seq_region_name":"7","id":"rs1796048552"},{"seq_region_name":"7","id":"rs557064321","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","G","T"],"end":140526181,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526181,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1384967308","clinical_significance":[],"start":140526182,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140526182,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140526183,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140526183,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796048893"},{"end":140526184,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140526184,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796048996","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796049095","clinical_significance":[],"start":140526186,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140526186,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796049200","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526190,"feature_type":"variation","strand":1,"end":140526190,"alleles":["T","A"]},{"end":140526193,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140526193,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796049305"},{"seq_region_name":"7","id":"rs1796049404","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526194,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140526194},{"start":140526195,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140526195,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1390160075","clinical_significance":[]},{"source":"dbSNP","start":140526196,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140526196,"alleles":["T","TT"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1298862292"},{"strand":1,"feature_type":"variation","end":140526197,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526197,"source":"dbSNP","seq_region_name":"7","id":"rs2130464479","clinical_significance":[]},{"end":140526200,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140526200,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs926431176","clinical_significance":[]},{"seq_region_name":"7","id":"rs1371509144","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526201,"source":"dbSNP","strand":1,"feature_type":"variation","end":140526201,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1796049936","clinical_significance":[],"start":140526204,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140526204,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1796050027","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526209,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140526209},{"seq_region_name":"7","id":"rs7792764","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140526210,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526210,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1158204094","clinical_significance":[],"alleles":["G","A"],"end":140526212,"strand":1,"feature_type":"variation","start":140526212,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1305766672","clinical_significance":[],"start":140526213,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140526213,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"id":"rs960286180","seq_region_name":"7","clinical_significance":[],"start":140526214,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140526214,"strand":1,"feature_type":"variation"},{"alleles":["G","A"],"end":140526216,"feature_type":"variation","strand":1,"source":"dbSNP","start":140526216,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796050538"},{"clinical_significance":[],"id":"rs1379679343","seq_region_name":"7","source":"dbSNP","start":140526216,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140526224,"alleles":["GAGGAGGAG","GAGGAG"],"feature_type":"variation","strand":1},{"start":140526217,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140526217,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796050750","clinical_significance":[]},{"alleles":["G","A"],"end":140526219,"feature_type":"variation","strand":1,"source":"dbSNP","start":140526219,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1197408596","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1349387707","end":140526221,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140526221,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526222,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140526222,"clinical_significance":[],"seq_region_name":"7","id":"rs781674086"},{"source":"dbSNP","start":140526232,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140526232,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1267631178","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140526234,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526234,"source":"dbSNP","seq_region_name":"7","id":"rs908582701","clinical_significance":[]},{"id":"rs1193755383","seq_region_name":"7","clinical_significance":[],"end":140526236,"alleles":["T","A","G"],"strand":1,"feature_type":"variation","start":140526236,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs6952208","clinical_significance":[],"end":140526238,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140526238,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526243,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140526243,"clinical_significance":[],"seq_region_name":"7","id":"rs1796051769"},{"seq_region_name":"7","id":"rs952403735","clinical_significance":[],"start":140526244,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140526244,"alleles":["C","G","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs756539925","clinical_significance":[],"strand":1,"feature_type":"variation","end":140526245,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526245,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1796052131","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526246,"source":"dbSNP","strand":1,"feature_type":"variation","end":140526246,"alleles":["G","A"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526261,"feature_type":"variation","strand":1,"end":140526261,"alleles":["T","C"],"clinical_significance":[],"id":"rs1257510824","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796052328","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526264,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140526264},{"start":140526268,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140526268,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1231040314","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140526269,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526269,"source":"dbSNP","seq_region_name":"7","id":"rs1796052530","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526272,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140526272,"clinical_significance":[],"seq_region_name":"7","id":"rs1796052644"},{"alleles":["G","A"],"end":140526273,"strand":1,"feature_type":"variation","start":140526273,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1796052751","seq_region_name":"7","clinical_significance":[]},{"start":140526274,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140526274,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs908268953","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140526275,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526275,"clinical_significance":[],"id":"rs1338631963","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130464752","source":"dbSNP","start":140526277,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140526277,"feature_type":"variation","strand":1},{"start":140526283,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["ATAAA","A"],"end":140526287,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796053073","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1330435898","feature_type":"variation","strand":1,"end":140526288,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526288},{"id":"rs2130464782","seq_region_name":"7","clinical_significance":[],"start":140526289,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140526289,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1796053291","clinical_significance":[],"strand":1,"feature_type":"variation","end":140526291,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526291,"source":"dbSNP"},{"alleles":["C","T"],"end":140526295,"feature_type":"variation","strand":1,"source":"dbSNP","start":140526295,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796053388"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1278989637","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526301,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140526301},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526304,"feature_type":"variation","strand":1,"end":140526304,"alleles":["C","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1796053593"},{"alleles":["A","C"],"end":140526317,"strand":1,"feature_type":"variation","start":140526317,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1243899266","clinical_significance":[]},{"alleles":["C","G"],"end":140526324,"strand":1,"feature_type":"variation","start":140526324,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796053806","clinical_significance":[]},{"id":"rs1338442188","seq_region_name":"7","clinical_significance":[],"start":140526336,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140526336,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526340,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140526340,"clinical_significance":[],"id":"rs932697253","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1796054142","clinical_significance":[],"alleles":["C","A"],"end":140526346,"strand":1,"feature_type":"variation","start":140526346,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1415214978","seq_region_name":"7","feature_type":"variation","strand":1,"end":140526349,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526349},{"seq_region_name":"7","id":"rs939743190","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140526353,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526353,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140526354,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526354,"source":"dbSNP","seq_region_name":"7","id":"rs1404847720","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1049942245","alleles":["G","A"],"end":140526356,"feature_type":"variation","strand":1,"source":"dbSNP","start":140526356,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1466039044","alleles":["C","A","T"],"end":140526357,"feature_type":"variation","strand":1,"source":"dbSNP","start":140526357,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140526361,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C","G"],"end":140526361,"strand":1,"feature_type":"variation","id":"rs1796054947","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796055043","alleles":["G","A"],"end":140526362,"feature_type":"variation","strand":1,"source":"dbSNP","start":140526362,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140526363,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140526363,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1270574147"},{"alleles":["C","A","T"],"end":140526364,"feature_type":"variation","strand":1,"source":"dbSNP","start":140526364,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs777961025"},{"seq_region_name":"7","id":"rs1478529925","clinical_significance":[],"start":140526365,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140526365,"strand":1,"feature_type":"variation"},{"alleles":["A","G"],"end":140526368,"strand":1,"feature_type":"variation","start":140526368,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs554570403","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130464973","source":"dbSNP","start":140526374,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140526374,"alleles":["C","T"],"feature_type":"variation","strand":1},{"alleles":["G","C"],"end":140526380,"feature_type":"variation","strand":1,"source":"dbSNP","start":140526380,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1158953895","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1796055682","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526385,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140526385},{"clinical_significance":[],"seq_region_name":"7","id":"rs6952414","end":140526391,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140526391,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1192077816","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140526394,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526394,"source":"dbSNP"},{"end":140526396,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140526396,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796056028","clinical_significance":[]},{"seq_region_name":"7","id":"rs377121765","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526399,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140526399},{"id":"rs114264595","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526400,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140526400},{"source":"dbSNP","start":140526401,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140526401,"alleles":["C","A","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1198508173","seq_region_name":"7"},{"seq_region_name":"7","id":"rs369393195","clinical_significance":[],"end":140526402,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140526402,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["A","C"],"end":140526403,"feature_type":"variation","strand":1,"source":"dbSNP","start":140526403,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585551498"},{"end":140526404,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140526404,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1796056737","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","G"],"end":140526405,"feature_type":"variation","strand":1,"source":"dbSNP","start":140526405,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs889151660"},{"id":"rs947389657","seq_region_name":"7","clinical_significance":[],"start":140526406,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140526406,"strand":1,"feature_type":"variation"},{"id":"rs1796057048","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140526407,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526407,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140526410,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526410,"source":"dbSNP","seq_region_name":"7","id":"rs1269636919","clinical_significance":[]},{"alleles":["A","G"],"end":140526413,"strand":1,"feature_type":"variation","start":140526413,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1043425100","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585551561","clinical_significance":[],"alleles":["A","C"],"end":140526415,"strand":1,"feature_type":"variation","start":140526415,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs903278542","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526416,"source":"dbSNP","strand":1,"feature_type":"variation","end":140526416,"alleles":["C","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs537188318","alleles":["C","G"],"end":140526417,"feature_type":"variation","strand":1,"source":"dbSNP","start":140526417,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140526422,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140526422,"alleles":["C","A","G"],"strand":1,"feature_type":"variation","id":"rs1035863178","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs895984791","clinical_significance":[],"start":140526426,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140526426,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1395826075","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140526427,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526427},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526431,"source":"dbSNP","strand":1,"feature_type":"variation","end":140526431,"alleles":["C","T"],"seq_region_name":"7","id":"rs1013208038","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140526435,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526435,"source":"dbSNP","seq_region_name":"7","id":"rs1796058168","clinical_significance":[]},{"alleles":["C","A","T"],"end":140526436,"strand":1,"feature_type":"variation","start":140526436,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs60213630","clinical_significance":[]},{"seq_region_name":"7","id":"rs1033476778","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526437,"source":"dbSNP","strand":1,"feature_type":"variation","end":140526437,"alleles":["G","A","T"]},{"seq_region_name":"7","id":"rs1796058571","clinical_significance":[],"start":140526439,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140526439,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs544797900","source":"dbSNP","start":140526441,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140526441,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs563394628","alleles":["G","A","T"],"end":140526442,"feature_type":"variation","strand":1,"source":"dbSNP","start":140526442,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526443,"source":"dbSNP","strand":1,"feature_type":"variation","end":140526443,"alleles":["G","A","C"],"seq_region_name":"7","id":"rs1369843362","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140526445,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526445,"source":"dbSNP","seq_region_name":"7","id":"rs2130465239","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140526446,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526446,"source":"dbSNP","id":"rs1796059047","seq_region_name":"7","clinical_significance":[]},{"id":"rs1184884359","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526449,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140526449},{"end":140526469,"alleles":["GCCAGGGGCCTGGATGGTC","-"],"strand":1,"feature_type":"variation","start":140526451,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1460719833","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796059322","alleles":["A","G"],"end":140526454,"feature_type":"variation","strand":1,"source":"dbSNP","start":140526454,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140526458,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526458,"source":"dbSNP","seq_region_name":"7","id":"rs983823097","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796059528","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526462,"feature_type":"variation","strand":1,"end":140526462,"alleles":["G","T"]},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140526473,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526473,"source":"dbSNP","seq_region_name":"7","id":"rs1585551696","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526477,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140526477,"clinical_significance":[],"id":"rs1238514042","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1391214552","clinical_significance":[],"start":140526480,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140526480,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1015648028","clinical_significance":[],"alleles":["C","T"],"end":140526483,"strand":1,"feature_type":"variation","start":140526483,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs908447287","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526485,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140526485},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140526489,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526489,"clinical_significance":[],"seq_region_name":"7","id":"rs758849376"},{"strand":1,"feature_type":"variation","alleles":["AT","-"],"end":140526492,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526491,"source":"dbSNP","seq_region_name":"7","id":"rs1228971059","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526493,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140526493,"id":"rs1166388254","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1245472201","source":"dbSNP","start":140526500,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140526500,"alleles":["C","A"],"feature_type":"variation","strand":1},{"id":"rs1378163202","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140526503,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526503,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796060626","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526509,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140526509},{"alleles":["A","G"],"end":140526512,"feature_type":"variation","strand":1,"source":"dbSNP","start":140526512,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1333763877"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796060812","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526513,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140526513},{"seq_region_name":"7","id":"rs1369550179","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526515,"source":"dbSNP","strand":1,"feature_type":"variation","end":140526515,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs961163210","feature_type":"variation","strand":1,"end":140526516,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526516},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526522,"feature_type":"variation","strand":1,"end":140526522,"alleles":["C","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1445291516"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526525,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140526525,"clinical_significance":[],"seq_region_name":"7","id":"rs2130465451"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130465457","source":"dbSNP","start":140526527,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140526527,"alleles":["A","AA"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1796061236","clinical_significance":[],"start":140526528,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140526528,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs976433298","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526529,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140526529},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526530,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140526530,"id":"rs961704213","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526530,"source":"dbSNP","strand":1,"feature_type":"variation","end":140526535,"alleles":["GGAGGG","GGAGGGAGGG"],"id":"rs1796061600","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1304093772","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140526531,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526531,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526533,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140526533,"seq_region_name":"7","id":"rs1796061808","clinical_significance":[]},{"seq_region_name":"7","id":"rs1399373376","clinical_significance":[],"start":140526537,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140526537,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs922481169","clinical_significance":[],"strand":1,"feature_type":"variation","end":140526539,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526539,"source":"dbSNP"},{"id":"rs1321102946","seq_region_name":"7","clinical_significance":[],"start":140526542,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140526542,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140526545,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526545,"clinical_significance":[],"seq_region_name":"7","id":"rs1796062122"},{"start":140526549,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140526549,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796062223","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526555,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140526555,"seq_region_name":"7","id":"rs1796062307","clinical_significance":[]},{"alleles":["C","T"],"end":140526556,"feature_type":"variation","strand":1,"source":"dbSNP","start":140526556,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796062404"},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140526558,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526558,"clinical_significance":[],"seq_region_name":"7","id":"rs530580851"},{"clinical_significance":[],"id":"rs1796062622","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526559,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140526559},{"clinical_significance":[],"id":"rs1415270956","seq_region_name":"7","source":"dbSNP","start":140526561,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140526561,"alleles":["A","T"],"feature_type":"variation","strand":1},{"alleles":["C","T"],"end":140526562,"strand":1,"feature_type":"variation","start":140526562,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs58690901","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs560769799","clinical_significance":[],"start":140526563,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140526563,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs528082039","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526567,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140526567},{"end":140526568,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140526568,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1180276604","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140526577,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526577,"source":"dbSNP","seq_region_name":"7","id":"rs1796063249","clinical_significance":[]},{"source":"dbSNP","start":140526582,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140526582,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1437521819"},{"clinical_significance":[],"seq_region_name":"7","id":"rs946595686","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140526587,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526587},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526588,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140526588,"clinical_significance":[],"seq_region_name":"7","id":"rs866917624"},{"id":"rs1796063640","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140526589,"strand":1,"feature_type":"variation","start":140526589,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526594,"source":"dbSNP","strand":1,"feature_type":"variation","end":140526594,"alleles":["G","A"],"seq_region_name":"7","id":"rs932752296","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140526596,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526596,"source":"dbSNP","seq_region_name":"7","id":"rs1796063861","clinical_significance":[]},{"source":"dbSNP","start":140526601,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140526601,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130465687"},{"seq_region_name":"7","id":"rs1585551989","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526603,"source":"dbSNP","strand":1,"feature_type":"variation","end":140526603,"alleles":["A","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1453433537","end":140526605,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140526605,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","T"],"end":140526610,"strand":1,"feature_type":"variation","start":140526610,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1796064223","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140526611,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140526611,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs867373707"},{"strand":1,"feature_type":"variation","end":140526613,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526613,"source":"dbSNP","seq_region_name":"7","id":"rs1585552025","clinical_significance":[]},{"end":140526615,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140526615,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs372341744","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526617,"feature_type":"variation","strand":1,"end":140526617,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1796064511"},{"seq_region_name":"7","id":"rs1043068604","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C","T"],"end":140526619,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526619,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526620,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140526620,"clinical_significance":[],"seq_region_name":"7","id":"rs1796064740"},{"clinical_significance":[],"id":"rs2130465762","seq_region_name":"7","source":"dbSNP","start":140526627,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140526627,"alleles":["T","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585552058","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526628,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140526628},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140526632,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526632,"source":"dbSNP","seq_region_name":"7","id":"rs1796064890","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140526645,"alleles":["GCACTGAAAGC","GC"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526635,"source":"dbSNP","seq_region_name":"7","id":"rs1796064995","clinical_significance":[]},{"end":140526638,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140526638,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs924566402","seq_region_name":"7"},{"end":140526639,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140526639,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1234181023","clinical_significance":[]},{"start":140526645,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140526645,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796065306","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796065410","clinical_significance":[],"start":140526646,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140526646,"strand":1,"feature_type":"variation"},{"id":"rs926145147","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526647,"source":"dbSNP","strand":1,"feature_type":"variation","end":140526647,"alleles":["C","T"]},{"feature_type":"variation","strand":1,"end":140526648,"alleles":["-","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526649,"clinical_significance":[],"id":"rs1796065630","seq_region_name":"7"},{"end":140526649,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140526649,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796065717","clinical_significance":[]},{"seq_region_name":"7","id":"rs1312003790","clinical_significance":[],"alleles":["C","T"],"end":140526654,"strand":1,"feature_type":"variation","start":140526654,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["G","A"],"end":140526655,"feature_type":"variation","strand":1,"source":"dbSNP","start":140526655,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs936154027"},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140526659,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526659,"clinical_significance":[],"seq_region_name":"7","id":"rs2130465880"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1372981104","end":140526662,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140526662,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130465896","feature_type":"variation","strand":1,"alleles":["G","-"],"end":140526665,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526665},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526669,"feature_type":"variation","strand":1,"end":140526669,"alleles":["A","G"],"clinical_significance":[],"id":"rs1275985208","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526670,"source":"dbSNP","strand":1,"feature_type":"variation","end":140526670,"alleles":["A","G"],"seq_region_name":"7","id":"rs1439168370","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140526674,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526674,"source":"dbSNP","seq_region_name":"7","id":"rs1053390329","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs892041241","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140526676,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526676},{"seq_region_name":"7","id":"rs77797887","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526677,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140526677},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796066805","alleles":["G","C"],"end":140526682,"feature_type":"variation","strand":1,"source":"dbSNP","start":140526682,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1046083800","source":"dbSNP","start":140526683,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140526683,"alleles":["A","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796067040","alleles":["C","G","T"],"end":140526688,"feature_type":"variation","strand":1,"source":"dbSNP","start":140526688,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs747574451","end":140526689,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140526689,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs2130466015","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526691,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140526691},{"clinical_significance":[],"seq_region_name":"7","id":"rs1057229636","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526693,"feature_type":"variation","strand":1,"end":140526693,"alleles":["C","G"]},{"clinical_significance":[],"id":"rs114545324","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526701,"feature_type":"variation","strand":1,"end":140526701,"alleles":["G","A","C"]},{"clinical_significance":[],"id":"rs1013072889","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526704,"feature_type":"variation","strand":1,"end":140526704,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1796067592","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526705,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140526705},{"id":"rs2130466058","seq_region_name":"7","clinical_significance":[],"start":140526710,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140526710,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526712,"source":"dbSNP","strand":1,"feature_type":"variation","end":140526712,"alleles":["T","C"],"seq_region_name":"7","id":"rs1044560212","clinical_significance":[]},{"seq_region_name":"7","id":"rs1406930084","clinical_significance":[],"strand":1,"feature_type":"variation","end":140526712,"alleles":["T","TT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526712,"source":"dbSNP"},{"clinical_significance":[],"id":"rs952570208","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526715,"feature_type":"variation","strand":1,"end":140526715,"alleles":["G","A","C"]},{"source":"dbSNP","start":140526716,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140526716,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1245117725","seq_region_name":"7"},{"start":140526723,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140526723,"strand":1,"feature_type":"variation","id":"rs1796068173","seq_region_name":"7","clinical_significance":[]},{"end":140526724,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140526724,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs115452035","clinical_significance":[]},{"end":140526726,"alleles":["C","A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140526726,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs6952999"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796068552","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140526727,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526727},{"feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140526730,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526730,"clinical_significance":[],"id":"rs1288440808","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130466164","source":"dbSNP","start":140526734,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140526734,"alleles":["G","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796068781","feature_type":"variation","strand":1,"end":140526736,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526736},{"alleles":["G","A","C"],"end":140526739,"feature_type":"variation","strand":1,"source":"dbSNP","start":140526739,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1796068874","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1796068993","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526741,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140526741},{"strand":1,"feature_type":"variation","end":140526743,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526743,"source":"dbSNP","id":"rs1466578966","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1214665958","seq_region_name":"7","feature_type":"variation","strand":1,"end":140526745,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526745},{"end":140526748,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140526748,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs2130466222","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs577391032","end":140526749,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140526749,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs111297382","clinical_significance":[],"start":140526750,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140526750,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1796069569","clinical_significance":[],"start":140526754,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G","T"],"end":140526754,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs2130466284","clinical_significance":[],"alleles":["C","T"],"end":140526756,"strand":1,"feature_type":"variation","start":140526756,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526757,"source":"dbSNP","strand":1,"feature_type":"variation","end":140526757,"alleles":["C","G"],"id":"rs1280883825","seq_region_name":"7","clinical_significance":[]},{"end":140526762,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140526762,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796069736","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796069818","clinical_significance":[],"start":140526763,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140526763,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796069910","source":"dbSNP","start":140526766,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140526766,"alleles":["C","T"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140526769,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526769,"source":"dbSNP","seq_region_name":"7","id":"rs536297525","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140526770,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526770,"clinical_significance":[],"seq_region_name":"7","id":"rs1796070100"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796070196","source":"dbSNP","start":140526774,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140526774,"alleles":["A","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1340548993","clinical_significance":[],"start":140526784,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140526784,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs2130466379","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526784,"source":"dbSNP","strand":1,"feature_type":"variation","end":140526786,"alleles":["TTT","TT"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585552329","source":"dbSNP","start":140526789,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140526789,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140526790,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140526790,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1433433505","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1428180234","source":"dbSNP","start":140526793,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140526793,"alleles":["C","T"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140526795,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140526795,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1344440254"},{"clinical_significance":[],"id":"rs1176508639","seq_region_name":"7","feature_type":"variation","strand":1,"end":140526805,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526805},{"seq_region_name":"7","id":"rs1416171745","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526806,"source":"dbSNP","strand":1,"feature_type":"variation","end":140526806,"alleles":["C","T"]},{"start":140526807,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140526807,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796070890","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140526808,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526808,"source":"dbSNP","seq_region_name":"7","id":"rs1427115155","clinical_significance":[]},{"source":"dbSNP","start":140526809,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140526809,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs73163298","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796071199","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526818,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140526818},{"clinical_significance":[],"id":"rs1796071287","seq_region_name":"7","end":140526822,"alleles":["CC","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140526821,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1796071396","clinical_significance":[],"alleles":["C","T"],"end":140526822,"strand":1,"feature_type":"variation","start":140526822,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140526825,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","G","T"],"end":140526825,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1375465545","clinical_significance":[]},{"end":140526826,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140526826,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs559073524","seq_region_name":"7","clinical_significance":[]},{"start":140526828,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140526828,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796071679","clinical_significance":[]},{"source":"dbSNP","start":140526836,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140526836,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796071760"},{"end":140526838,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140526838,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1265379087"},{"clinical_significance":[],"id":"rs1029356856","seq_region_name":"7","alleles":["G","A"],"end":140526844,"feature_type":"variation","strand":1,"source":"dbSNP","start":140526844,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140526852,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140526852,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796072035"},{"id":"rs1796072125","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140526854,"strand":1,"feature_type":"variation","start":140526854,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1485650830","alleles":["G","A","C"],"end":140526857,"feature_type":"variation","strand":1,"source":"dbSNP","start":140526857,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140526859,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140526859,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs2130466641","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140526866,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526866,"source":"dbSNP","seq_region_name":"7","id":"rs1238467572","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140526868,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526868,"clinical_significance":[],"id":"rs762445044","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1796072524","clinical_significance":[],"end":140526874,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140526874,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796072609","source":"dbSNP","start":140526875,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140526875,"alleles":["T","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1585552477","clinical_significance":[],"start":140526882,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140526882,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140526884,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526884,"source":"dbSNP","seq_region_name":"7","id":"rs985584795","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140526887,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526887,"source":"dbSNP","seq_region_name":"7","id":"rs1796072908","clinical_significance":[]},{"start":140526888,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140526888,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1321217100","clinical_significance":[]},{"seq_region_name":"7","id":"rs1465098432","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["TTT","TTTT"],"end":140526890,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526888,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs926011170","source":"dbSNP","start":140526889,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140526889,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs573194901","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526890,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140526890},{"seq_region_name":"7","id":"rs1796073389","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526892,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140526892},{"end":140526894,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140526894,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs534181783","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140526895,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526895,"clinical_significance":[],"seq_region_name":"7","id":"rs116654006"},{"alleles":["C","G"],"end":140526896,"feature_type":"variation","strand":1,"source":"dbSNP","start":140526896,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796073698"},{"start":140526899,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140526899,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","id":"rs915023047","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs913368490","clinical_significance":[],"end":140526900,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140526900,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526904,"source":"dbSNP","strand":1,"feature_type":"variation","end":140526904,"alleles":["C","T"],"seq_region_name":"7","id":"rs1279515891","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796074083","alleles":["T","C"],"end":140526905,"feature_type":"variation","strand":1,"source":"dbSNP","start":140526905,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526906,"source":"dbSNP","strand":1,"feature_type":"variation","end":140526906,"alleles":["A","C","T"],"seq_region_name":"7","id":"rs1380229006","clinical_significance":[]},{"end":140526911,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140526911,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs967994184"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796074254","end":140526912,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140526912,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140526914,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526914,"source":"dbSNP","seq_region_name":"7","id":"rs577585052","clinical_significance":[]},{"start":140526915,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140526915,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1387606174","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1046371007","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526916,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140526916},{"source":"dbSNP","start":140526918,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140526918,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1449965572"},{"seq_region_name":"7","id":"rs906233849","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526921,"source":"dbSNP","strand":1,"feature_type":"variation","end":140526921,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs1796074880","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140526923,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526923,"source":"dbSNP"},{"source":"dbSNP","start":140526924,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140526924,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796074980"},{"start":140526924,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TTGG","-"],"end":140526927,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs780265765","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140526926,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526926,"source":"dbSNP","seq_region_name":"7","id":"rs544834504","clinical_significance":[]},{"alleles":["GGGG","GG"],"end":140526929,"strand":1,"feature_type":"variation","start":140526926,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1466047133","clinical_significance":[]},{"seq_region_name":"7","id":"rs1054829428","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526928,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140526928},{"seq_region_name":"7","id":"rs888209352","clinical_significance":[],"end":140526930,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140526930,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140526931,"alleles":["T","TGCTAAACT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526931,"clinical_significance":[],"seq_region_name":"7","id":"rs1796075607"},{"seq_region_name":"7","id":"rs1005233963","clinical_significance":[],"end":140526940,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140526940,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs924669058","seq_region_name":"7","clinical_significance":[],"start":140526947,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","T"],"end":140526947,"strand":1,"feature_type":"variation"},{"id":"rs189691530","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526948,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140526948},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796076007","alleles":["C","T"],"end":140526956,"feature_type":"variation","strand":1,"source":"dbSNP","start":140526956,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1057261766","source":"dbSNP","start":140526957,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140526957,"alleles":["A","G"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140526959,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140526959,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs559883612"},{"seq_region_name":"7","id":"rs948755809","clinical_significance":[],"start":140526960,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140526960,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"id":"rs1796076367","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140526963,"strand":1,"feature_type":"variation","start":140526963,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1796076467","clinical_significance":[],"end":140526964,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140526964,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140526967,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140526967,"alleles":["A","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1029992908","seq_region_name":"7"},{"start":140526969,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140526969,"alleles":["C","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1044579738","clinical_significance":[]},{"start":140526971,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140526971,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1229635250","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796076866","end":140526972,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140526972,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1192615316","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140526974,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526974,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1314077092","source":"dbSNP","start":140526976,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140526976,"alleles":["G","A"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526980,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140526980,"clinical_significance":[],"id":"rs888576079","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1796077410","clinical_significance":[],"start":140526984,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140526984,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1402361193","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140526985,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526985},{"source":"dbSNP","start":140526986,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140526986,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1264823094"},{"alleles":["G","A"],"end":140526988,"feature_type":"variation","strand":1,"source":"dbSNP","start":140526988,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1461567368"},{"feature_type":"variation","strand":1,"end":140526990,"alleles":["G","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526990,"clinical_significance":[],"seq_region_name":"7","id":"rs1432171451"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796078130","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140526993,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526993},{"seq_region_name":"7","id":"rs1005843347","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140526994,"source":"dbSNP","strand":1,"feature_type":"variation","end":140526994,"alleles":["G","A"]},{"feature_type":"variation","strand":1,"end":140526999,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140526999,"clinical_significance":[],"id":"rs1390581955","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1385067083","end":140527000,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140527000,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527002,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140527002,"clinical_significance":[],"seq_region_name":"7","id":"rs1037684540"},{"seq_region_name":"7","id":"rs143971287","clinical_significance":[],"start":140527004,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140527004,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140527005,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140527005,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1796078855","seq_region_name":"7"},{"seq_region_name":"7","id":"rs374424646","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527006,"source":"dbSNP","strand":1,"feature_type":"variation","end":140527006,"alleles":["G","A","T"]},{"strand":1,"feature_type":"variation","end":140527008,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527008,"source":"dbSNP","id":"rs561020847","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140527009,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527009,"clinical_significance":[],"seq_region_name":"7","id":"rs528101017"},{"clinical_significance":[],"id":"rs927523614","seq_region_name":"7","source":"dbSNP","start":140527014,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140527014,"alleles":["G","C"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527015,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140527015,"id":"rs1796079326","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140527016,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527016,"clinical_significance":[],"seq_region_name":"7","id":"rs889538369"},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140527017,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527017,"source":"dbSNP","id":"rs1006553936","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796079593","clinical_significance":[],"start":140527022,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140527022,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs74329726","clinical_significance":[],"strand":1,"feature_type":"variation","end":140527023,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527023,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1223379324","clinical_significance":[],"alleles":["A","G"],"end":140527026,"strand":1,"feature_type":"variation","start":140527026,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527032,"feature_type":"variation","strand":1,"end":140527032,"alleles":["G","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs772711861"},{"start":140527035,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140527036,"alleles":["TT","-"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1563117748","clinical_significance":[]},{"id":"rs1796080350","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527037,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140527037},{"seq_region_name":"7","id":"rs1796080503","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["TTTT","TTT"],"end":140527045,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527042,"source":"dbSNP"},{"end":140527046,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140527046,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1356802192","seq_region_name":"7"},{"alleles":["A","G"],"end":140527049,"strand":1,"feature_type":"variation","start":140527049,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796080783","clinical_significance":[]},{"seq_region_name":"7","id":"rs1314192336","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527050,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140527050},{"strand":1,"feature_type":"variation","end":140527051,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527051,"source":"dbSNP","id":"rs1365758173","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140527052,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527052,"source":"dbSNP","seq_region_name":"7","id":"rs1796081220","clinical_significance":[]},{"seq_region_name":"7","id":"rs1054737419","clinical_significance":[],"start":140527053,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C"],"end":140527053,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140527054,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140527054,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796081504"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1390722588","feature_type":"variation","strand":1,"end":140527057,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527057},{"alleles":["T","C"],"end":140527060,"strand":1,"feature_type":"variation","start":140527060,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs888071670","clinical_significance":[]},{"clinical_significance":[],"id":"rs1295348327","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140527062,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527062},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796082093","feature_type":"variation","strand":1,"end":140527063,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527063},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527065,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140527065,"id":"rs2130467416","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","C"],"end":140527067,"feature_type":"variation","strand":1,"source":"dbSNP","start":140527067,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1423050235"},{"source":"dbSNP","start":140527075,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140527075,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1289090975"},{"end":140527079,"alleles":["CTTCT","CT"],"strand":1,"feature_type":"variation","start":140527075,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1404500339","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527084,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140527084,"seq_region_name":"7","id":"rs564849425","clinical_significance":[]},{"seq_region_name":"7","id":"rs1362381639","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140527085,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527085,"source":"dbSNP"},{"alleles":["GG","GGG"],"end":140527086,"strand":1,"feature_type":"variation","start":140527085,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs941120018","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796083176","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527086,"source":"dbSNP","strand":1,"feature_type":"variation","end":140527086,"alleles":["G","A"]},{"clinical_significance":[],"id":"rs1227133441","seq_region_name":"7","feature_type":"variation","strand":1,"end":140527094,"alleles":["A","C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527094},{"end":140527096,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140527096,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1434236380","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140527101,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527101,"source":"dbSNP","id":"rs114785488","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs978063435","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527102,"source":"dbSNP","strand":1,"feature_type":"variation","end":140527102,"alleles":["T","A","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1031317194","alleles":["T","A"],"end":140527107,"feature_type":"variation","strand":1,"source":"dbSNP","start":140527107,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140527114,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527114,"clinical_significance":[],"seq_region_name":"7","id":"rs1290591761"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796084109","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527117,"feature_type":"variation","strand":1,"end":140527120,"alleles":["AAAA","AAA"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527120,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140527120,"clinical_significance":[],"seq_region_name":"7","id":"rs75675261"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527122,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AG","-"],"end":140527123,"seq_region_name":"7","id":"rs1352627128","clinical_significance":[]},{"clinical_significance":[],"id":"rs1796084453","seq_region_name":"7","feature_type":"variation","strand":1,"end":140527123,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527123},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140527125,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527125,"source":"dbSNP","id":"rs1563117803","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs568761612","feature_type":"variation","strand":1,"end":140527129,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527129},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796084704","alleles":["T","G"],"end":140527133,"feature_type":"variation","strand":1,"source":"dbSNP","start":140527133,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140527136,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140527136,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1490090929","clinical_significance":[]},{"start":140527139,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140527139,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs889717608","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796084978","source":"dbSNP","start":140527142,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140527142,"feature_type":"variation","strand":1},{"start":140527146,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140527146,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1006790773","clinical_significance":[]},{"id":"rs1585553194","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140527148,"strand":1,"feature_type":"variation","start":140527148,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs992842079","source":"dbSNP","start":140527155,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140527155,"alleles":["A","G"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140527157,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527157,"clinical_significance":[],"id":"rs1796085348","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140527158,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527158,"clinical_significance":[],"seq_region_name":"7","id":"rs1796085491"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527160,"feature_type":"variation","strand":1,"end":140527160,"alleles":["C","T"],"clinical_significance":[],"id":"rs1796085582","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140527165,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527165,"source":"dbSNP","seq_region_name":"7","id":"rs1796085674","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1253403017","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527168,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140527168},{"start":140527170,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140527170,"alleles":["C","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs957324292","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527173,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140527173,"clinical_significance":[],"seq_region_name":"7","id":"rs1471313170"},{"start":140527174,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140527174,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs1344911098","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1299063036","clinical_significance":[],"strand":1,"feature_type":"variation","end":140527178,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527178,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527179,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140527179,"clinical_significance":[],"id":"rs1585553274","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140527180,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527180,"clinical_significance":[],"id":"rs1796086295","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1402045613","clinical_significance":[],"alleles":["C","T"],"end":140527181,"strand":1,"feature_type":"variation","start":140527181,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["G","C"],"end":140527191,"feature_type":"variation","strand":1,"source":"dbSNP","start":140527191,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1383320303"},{"seq_region_name":"7","id":"rs988929378","clinical_significance":[],"end":140527193,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140527193,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140527194,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140527194,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1467061873"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796086694","feature_type":"variation","strand":1,"end":140527198,"alleles":["CCCCC","CCCC"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527194},{"clinical_significance":[],"seq_region_name":"7","id":"rs917222121","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527196,"feature_type":"variation","strand":1,"end":140527196,"alleles":["C","T"]},{"start":140527197,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140527197,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1406950004","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527198,"feature_type":"variation","strand":1,"end":140527198,"alleles":["C","G"],"clinical_significance":[],"id":"rs1796086943","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527199,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140527199,"seq_region_name":"7","id":"rs1162443393","clinical_significance":[]},{"end":140527200,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140527200,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1479181495","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527201,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140527201,"seq_region_name":"7","id":"rs1020786213","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140527204,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527204,"clinical_significance":[],"seq_region_name":"7","id":"rs1424296706"},{"clinical_significance":[],"seq_region_name":"7","id":"rs948786767","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527207,"feature_type":"variation","strand":1,"end":140527207,"alleles":["C","T"]},{"alleles":["C","T"],"end":140527209,"feature_type":"variation","strand":1,"source":"dbSNP","start":140527209,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs529891596"},{"source":"dbSNP","start":140527210,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140527210,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1796087930","seq_region_name":"7"},{"end":140527211,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140527211,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1259486478"},{"id":"rs2130467859","seq_region_name":"7","clinical_significance":[],"start":140527217,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140527217,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1796088180","clinical_significance":[],"end":140527224,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140527224,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs2130467882","seq_region_name":"7","alleles":["C","G"],"end":140527226,"feature_type":"variation","strand":1,"source":"dbSNP","start":140527226,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["A","C"],"end":140527229,"strand":1,"feature_type":"variation","start":140527229,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796088321","clinical_significance":[]},{"end":140527234,"alleles":["CC","C"],"strand":1,"feature_type":"variation","start":140527233,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130467901","clinical_significance":[]},{"alleles":["C","T"],"end":140527234,"feature_type":"variation","strand":1,"source":"dbSNP","start":140527234,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs910086829"},{"end":140527235,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140527235,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs548429269","clinical_significance":[]},{"seq_region_name":"7","id":"rs1037312662","clinical_significance":[],"strand":1,"feature_type":"variation","end":140527238,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527238,"source":"dbSNP"},{"seq_region_name":"7","id":"rs897423620","clinical_significance":[],"end":140527239,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140527239,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs934208426","seq_region_name":"7","source":"dbSNP","start":140527241,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140527241,"alleles":["T","C"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140527246,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527246,"source":"dbSNP","seq_region_name":"7","id":"rs566936961","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796089252","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527248,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140527248},{"strand":1,"feature_type":"variation","end":140527255,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527255,"source":"dbSNP","seq_region_name":"7","id":"rs927460652","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1220751488","source":"dbSNP","start":140527259,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140527259,"alleles":["C","A","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs889445952","clinical_significance":[],"alleles":["G","A","C"],"end":140527260,"strand":1,"feature_type":"variation","start":140527260,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1324903957","clinical_significance":[],"strand":1,"feature_type":"variation","end":140527264,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527264,"source":"dbSNP"},{"end":140527265,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140527265,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs533962579","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796089886","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140527268,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527268},{"id":"rs1796089970","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140527270,"alleles":["G","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527270,"source":"dbSNP"},{"id":"rs1796090059","seq_region_name":"7","clinical_significance":[],"end":140527273,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140527273,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527276,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140527276,"seq_region_name":"7","id":"rs2293178","clinical_significance":[]},{"seq_region_name":"7","id":"rs377015181","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527277,"source":"dbSNP","strand":1,"feature_type":"variation","end":140527277,"alleles":["G","A"]},{"end":140527279,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140527279,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1437709673"},{"source":"dbSNP","start":140527281,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140527281,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1365194816"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527284,"source":"dbSNP","strand":1,"feature_type":"variation","end":140527284,"alleles":["G","A"],"seq_region_name":"7","id":"rs1796090630","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140527285,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527285,"clinical_significance":[],"seq_region_name":"7","id":"rs1468363510"},{"clinical_significance":[],"id":"rs2130468096","seq_region_name":"7","source":"dbSNP","start":140527286,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140527286,"feature_type":"variation","strand":1},{"id":"rs1158187479","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527288,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140527288},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527291,"source":"dbSNP","strand":1,"feature_type":"variation","end":140527291,"alleles":["G","A","C"],"id":"rs1395087125","seq_region_name":"7","clinical_significance":[]},{"start":140527292,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140527292,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1469719637","clinical_significance":[]},{"id":"rs772982645","seq_region_name":"7","clinical_significance":[],"end":140527294,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140527294,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140527296,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140527296,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs760450334"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796091229","source":"dbSNP","start":140527296,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","AA"],"end":140527296,"feature_type":"variation","strand":1},{"start":140527297,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140527297,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs1323958862","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527298,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140527298,"id":"rs1796091414","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140527299,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140527299,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1170768156","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs765879366","end":140527301,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140527301,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140527302,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527302,"source":"dbSNP","seq_region_name":"7","id":"rs909585034","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796091830","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527304,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140527304},{"alleles":["G","C"],"end":140527308,"strand":1,"feature_type":"variation","start":140527308,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796091924","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs776034788","consequence_type":"splice_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527311,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140527311},{"assembly_name":"GRCh38","consequence_type":"splice_donor_region_variant","start":140527315,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140527315,"seq_region_name":"7","id":"rs1191969939","clinical_significance":[]},{"alleles":["C","T"],"end":140527323,"strand":1,"feature_type":"variation","start":140527323,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs1796092182","clinical_significance":[]},{"id":"rs376931201","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140527327,"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140527327,"source":"dbSNP"},{"seq_region_name":"7","id":"rs765675447","clinical_significance":[],"start":140527328,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140527328,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs2486064641","clinical_significance":["uncertain significance"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140527331,"source":"ClinVar","strand":1,"feature_type":"variation","end":140527331,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1294336943","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527332,"feature_type":"variation","strand":1,"end":140527332,"alleles":["G","A","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs753039704","feature_type":"variation","strand":1,"end":140527333,"alleles":["C","G"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527333},{"strand":1,"feature_type":"variation","end":140527334,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140527334,"source":"dbSNP","seq_region_name":"7","id":"rs758758842","clinical_significance":[]},{"start":140527335,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140527335,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs764502827","clinical_significance":[]},{"seq_region_name":"7","id":"rs1201742747","clinical_significance":[],"start":140527336,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140527336,"alleles":["C","G","T"],"strand":1,"feature_type":"variation"},{"alleles":["C","G"],"end":140527337,"strand":1,"feature_type":"variation","start":140527337,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs751760395","clinical_significance":[]},{"id":"rs757513986","seq_region_name":"7","clinical_significance":[],"start":140527338,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140527338,"alleles":["T","C","G"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["GAG","GAGAAGTGGCAGCGAGCTGGAGAG"],"end":140527341,"assembly_name":"GRCh38","consequence_type":"inframe_insertion","start":140527339,"source":"dbSNP","seq_region_name":"7","id":"rs764719401","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140527341,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140527341,"seq_region_name":"7","id":"rs745960831","clinical_significance":[]},{"seq_region_name":"7","id":"rs371061412","clinical_significance":[],"alleles":["G","A"],"end":140527344,"strand":1,"feature_type":"variation","start":140527344,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant"},{"end":140527345,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140527345,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","seq_region_name":"7","id":"rs778708177","clinical_significance":[]},{"seq_region_name":"7","id":"rs11553487","clinical_significance":[],"end":140527347,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140527347,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"clinical_significance":[],"id":"rs1418380883","seq_region_name":"7","consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527348,"feature_type":"variation","strand":1,"end":140527348,"alleles":["C","T"]},{"strand":1,"feature_type":"variation","end":140527352,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140527352,"source":"dbSNP","seq_region_name":"7","id":"rs1476144652","clinical_significance":[]},{"seq_region_name":"7","id":"rs1162786138","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140527353,"source":"dbSNP","strand":1,"feature_type":"variation","end":140527353,"alleles":["A","G"]},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527358,"feature_type":"variation","strand":1,"alleles":["G","A","C","T"],"end":140527358,"clinical_significance":[],"seq_region_name":"7","id":"rs372774479"},{"seq_region_name":"7","id":"rs1462601819","clinical_significance":[],"start":140527360,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","end":140527360,"alleles":["G","A","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1299931267","feature_type":"variation","strand":1,"end":140527361,"alleles":["A","G"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527361},{"clinical_significance":[],"seq_region_name":"7","id":"rs1385501569","source":"dbSNP","start":140527362,"consequence_type":"frameshift_variant","assembly_name":"GRCh38","end":140527361,"alleles":["-","TGAG"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"frameshift_variant","start":140527367,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["-","GAG","GAGCAGTGGCA"],"end":140527366,"seq_region_name":"7","id":"rs1796094678","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1313356593","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140527367,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527367},{"seq_region_name":"7","id":"rs746618150","clinical_significance":[],"end":140527368,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140527368,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527369,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140527369,"clinical_significance":[],"id":"rs375568987","seq_region_name":"7"},{"consequence_type":"frameshift_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527370,"feature_type":"variation","strand":1,"end":140527370,"alleles":["A","-"],"clinical_significance":[],"seq_region_name":"7","id":"rs774995503"},{"clinical_significance":[],"seq_region_name":"7","id":"rs542386012","end":140527371,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140527371,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs368218935","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140527372,"source":"dbSNP","strand":1,"feature_type":"variation","end":140527372,"alleles":["G","A"]},{"id":"rs770511346","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140527374,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140527374,"source":"dbSNP"},{"seq_region_name":"7","id":"rs2130468554","clinical_significance":[],"start":140527379,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["G","A"],"end":140527379,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140527381,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140527381,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs370709180"},{"end":140527382,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140527382,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs373863707","clinical_significance":["uncertain significance"]},{"id":"rs76760136","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140527384,"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140527384,"source":"dbSNP"},{"source":"dbSNP","start":140527385,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140527385,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs893181775"},{"source":"dbSNP","start":140527387,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","end":140527387,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1010228220"},{"assembly_name":"GRCh38","consequence_type":"stop_gained","start":140527388,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140527388,"seq_region_name":"7","id":"rs1227560734","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1181516336","alleles":["G","C"],"end":140527390,"feature_type":"variation","strand":1,"source":"dbSNP","start":140527390,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527391,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140527391,"clinical_significance":[],"seq_region_name":"7","id":"rs1443711661"},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140527392,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140527392,"seq_region_name":"7","id":"rs775964284","clinical_significance":["uncertain significance"]},{"source":"dbSNP","start":140527393,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","end":140527393,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1339650625"},{"start":140527394,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["A","G"],"end":140527394,"strand":1,"feature_type":"variation","id":"rs1231389573","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1203911611","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140527395,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140527395},{"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140527396,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140527396,"seq_region_name":"7","id":"rs1257774081","clinical_significance":[]},{"clinical_significance":[],"id":"rs971906388","seq_region_name":"7","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527398,"feature_type":"variation","strand":1,"end":140527398,"alleles":["T","C"]},{"alleles":["C","T"],"end":140527401,"strand":1,"feature_type":"variation","start":140527401,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","id":"rs371401607","seq_region_name":"7","clinical_significance":["uncertain significance"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs764413244","feature_type":"variation","strand":1,"end":140527402,"alleles":["G","A","C"],"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527402},{"seq_region_name":"7","id":"rs751954587","clinical_significance":[],"start":140527406,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["A","G"],"end":140527406,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1796097633","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140527407,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140527407},{"start":140527408,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","end":140527408,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs970040736","clinical_significance":[]},{"seq_region_name":"7","id":"rs200369917","clinical_significance":[],"strand":1,"feature_type":"variation","end":140527410,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140527410,"source":"dbSNP"},{"seq_region_name":"7","id":"rs199555273","clinical_significance":[],"end":140527411,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140527411,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant"},{"seq_region_name":"7","id":"rs767651224","clinical_significance":[],"strand":1,"feature_type":"variation","end":140527412,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140527412,"source":"dbSNP"},{"source":"dbSNP","start":140527413,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140527413,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796098162"},{"seq_region_name":"7","id":"rs750719538","clinical_significance":[],"alleles":["T","G"],"end":140527414,"strand":1,"feature_type":"variation","start":140527414,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant"},{"seq_region_name":"7","id":"rs1796098365","clinical_significance":[],"alleles":["G","A"],"end":140527415,"strand":1,"feature_type":"variation","start":140527415,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140527417,"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140527417,"source":"dbSNP","id":"rs756130811","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140527417,"consequence_type":"frameshift_variant","assembly_name":"GRCh38","alleles":["CA","-"],"end":140527418,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1585554074","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1377483195","clinical_significance":[],"start":140527417,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"frameshift_variant","alleles":["CAGCACC","-"],"end":140527423,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585554095","feature_type":"variation","strand":1,"end":140527423,"alleles":["CACC","-"],"consequence_type":"frameshift_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527420},{"clinical_significance":[],"id":"rs909941466","seq_region_name":"7","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527422,"feature_type":"variation","strand":1,"end":140527422,"alleles":["C","G"]},{"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527423,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140527423,"clinical_significance":[],"seq_region_name":"7","id":"rs780228497"},{"end":140527424,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140527424,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1363298192","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1796099165","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140527425,"source":"dbSNP","strand":1,"feature_type":"variation","end":140527425,"alleles":["G","T"]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140527428,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"ClinVar","start":140527428,"clinical_significance":["uncertain significance"],"id":"rs2486065407","seq_region_name":"7"},{"end":140527434,"alleles":["T","A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140527434,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1384360611"},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140527438,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140527438,"source":"dbSNP","id":"rs752648311","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140527444,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140527444,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs758439481"},{"clinical_significance":["likely benign"],"seq_region_name":"7","id":"rs777661670","source":"dbSNP","start":140527446,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140527446,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs770559076","alleles":["G","A"],"end":140527447,"feature_type":"variation","strand":1,"source":"dbSNP","start":140527447,"consequence_type":"synonymous_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140527453,"alleles":["G","T"],"consequence_type":"stop_gained","assembly_name":"GRCh38","source":"dbSNP","start":140527453,"clinical_significance":[],"id":"rs780694689","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1045975514","seq_region_name":"7","end":140527454,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140527454,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1207790535","clinical_significance":[],"start":140527456,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","alleles":["G","A"],"end":140527456,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs745600490","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527458,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140527458},{"start":140527459,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","end":140527459,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs769154200","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs775027767","feature_type":"variation","strand":1,"end":140527462,"alleles":["C","T"],"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527462},{"seq_region_name":"7","id":"rs763399697","clinical_significance":[],"strand":1,"feature_type":"variation","end":140527463,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140527463,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140527471,"alleles":["C","A","T"],"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527471,"clinical_significance":[],"seq_region_name":"7","id":"rs769179634"},{"start":140527472,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140527472,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1194307029","clinical_significance":["uncertain significance"]},{"feature_type":"variation","strand":1,"end":140527473,"alleles":["C","A","T"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527473,"clinical_significance":["uncertain significance"],"seq_region_name":"7","id":"rs774627233"},{"clinical_significance":[],"seq_region_name":"7","id":"rs376819636","alleles":["G","A"],"end":140527474,"feature_type":"variation","strand":1,"source":"dbSNP","start":140527474,"consequence_type":"synonymous_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140527476,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140527476,"seq_region_name":"7","id":"rs1175815125","clinical_significance":[]},{"consequence_type":"frameshift_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527476,"feature_type":"variation","strand":1,"alleles":["GG","G"],"end":140527477,"clinical_significance":[],"id":"rs2130469028","seq_region_name":"7"},{"end":140527477,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140527477,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs767996612"},{"seq_region_name":"7","id":"rs750583752","clinical_significance":[],"strand":1,"feature_type":"variation","end":140527486,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140527486,"source":"dbSNP"},{"alleles":["C","T"],"end":140527489,"strand":1,"feature_type":"variation","start":140527489,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","seq_region_name":"7","id":"rs761009784","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1178917895","source":"dbSNP","start":140527491,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140527491,"feature_type":"variation","strand":1},{"alleles":["G","A","T"],"end":140527492,"feature_type":"variation","strand":1,"source":"dbSNP","start":140527492,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs766520796","seq_region_name":"7"},{"seq_region_name":"7","id":"rs6464833","clinical_significance":[],"strand":1,"feature_type":"variation","end":140527493,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140527493,"source":"dbSNP"},{"id":"rs972824891","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140527495,"strand":1,"feature_type":"variation","start":140527495,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_region_variant"},{"alleles":["C","G","T"],"end":140527496,"strand":1,"feature_type":"variation","start":140527496,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_acceptor_variant","seq_region_name":"7","id":"rs942342577","clinical_significance":[]},{"consequence_type":"splice_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527498,"feature_type":"variation","strand":1,"end":140527498,"alleles":["G","A"],"clinical_significance":[],"id":"rs1303447265","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1639872325","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140527502,"consequence_type":"splice_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527502},{"id":"rs762395989","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"splice_region_variant","start":140527502,"source":"dbSNP","strand":1,"feature_type":"variation","end":140527503,"alleles":["CC","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1217052253","feature_type":"variation","strand":1,"end":140527503,"alleles":["C","T"],"consequence_type":"splice_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527503},{"clinical_significance":[],"seq_region_name":"7","id":"rs375196042","end":140527504,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140527504,"consequence_type":"splice_polypyrimidine_tract_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs764141635","seq_region_name":"7","end":140527505,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140527505,"consequence_type":"splice_polypyrimidine_tract_variant","assembly_name":"GRCh38"},{"consequence_type":"splice_polypyrimidine_tract_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527507,"feature_type":"variation","strand":1,"end":140527507,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1796104135"},{"consequence_type":"splice_polypyrimidine_tract_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527510,"feature_type":"variation","strand":1,"end":140527510,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs933740064"},{"end":140527511,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140527511,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_polypyrimidine_tract_variant","seq_region_name":"7","id":"rs1217654666","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527514,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140527514,"id":"rs1354921633","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs531979786","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527518,"source":"dbSNP","strand":1,"feature_type":"variation","end":140527518,"alleles":["G","A","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs544143678","feature_type":"variation","strand":1,"end":140527519,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527519},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527520,"source":"dbSNP","strand":1,"feature_type":"variation","end":140527520,"alleles":["G","A"],"seq_region_name":"7","id":"rs2130469272","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1214422426","end":140527521,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140527521,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","G","T"],"end":140527527,"feature_type":"variation","strand":1,"source":"dbSNP","start":140527527,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs562427753"},{"clinical_significance":[],"seq_region_name":"7","id":"rs754490449","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527528,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140527528},{"seq_region_name":"7","id":"rs911092450","clinical_significance":[],"start":140527534,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140527534,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527535,"feature_type":"variation","strand":1,"end":140527535,"alleles":["C","T"],"clinical_significance":[],"id":"rs529876522","seq_region_name":"7"},{"seq_region_name":"7","id":"rs768009898","clinical_significance":[],"start":140527536,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140527536,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs942509080","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527538,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140527538},{"clinical_significance":[],"seq_region_name":"7","id":"rs769089755","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527539,"feature_type":"variation","strand":1,"end":140527539,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1346794146","end":140527540,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140527540,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527543,"source":"dbSNP","strand":1,"feature_type":"variation","end":140527543,"alleles":["C","G","T"],"seq_region_name":"7","id":"rs369401539","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A","C","T"],"end":140527544,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527544,"clinical_significance":[],"seq_region_name":"7","id":"rs748733944"},{"start":140527546,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140527546,"alleles":["G","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1326008220","clinical_significance":[]},{"clinical_significance":[],"id":"rs1398669520","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140527549,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527549},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796107632","end":140527550,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140527550,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140527552,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527552,"source":"dbSNP","seq_region_name":"7","id":"rs1407181869","clinical_significance":[]},{"end":140527553,"alleles":["T","-"],"strand":1,"feature_type":"variation","start":140527553,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130469413","clinical_significance":[]},{"start":140527556,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140527556,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796107942","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796108084","clinical_significance":[],"end":140527556,"alleles":["A","-"],"strand":1,"feature_type":"variation","start":140527556,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["G","A"],"end":140527559,"strand":1,"feature_type":"variation","start":140527559,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs759687831","clinical_significance":[]},{"seq_region_name":"7","id":"rs1013544362","clinical_significance":[],"end":140527560,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140527560,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140527561,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140527561,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1023545495","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130469475","alleles":["AGGCTCCTCCCAG","AG"],"end":140527576,"feature_type":"variation","strand":1,"source":"dbSNP","start":140527564,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140527566,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527566,"source":"dbSNP","seq_region_name":"7","id":"rs1796108738","clinical_significance":[]},{"start":140527567,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140527567,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796108925","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130469509","feature_type":"variation","strand":1,"end":140527569,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527569},{"seq_region_name":"7","id":"rs1481479847","clinical_significance":[],"start":140527570,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140527570,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140527572,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527572,"source":"dbSNP","seq_region_name":"7","id":"rs1042113220","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140527573,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527573,"clinical_significance":[],"seq_region_name":"7","id":"rs1266828381"},{"strand":1,"feature_type":"variation","end":140527578,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527578,"source":"dbSNP","id":"rs1796109574","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130469548","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527579,"source":"dbSNP","strand":1,"feature_type":"variation","end":140527579,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs753263143","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527580,"feature_type":"variation","strand":1,"end":140527580,"alleles":["C","T"]},{"feature_type":"variation","strand":1,"end":140527581,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527581,"clinical_significance":[],"seq_region_name":"7","id":"rs1796109856"},{"clinical_significance":[],"seq_region_name":"7","id":"rs970072158","end":140527583,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140527583,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1388040308","feature_type":"variation","strand":1,"end":140527585,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527585},{"feature_type":"variation","strand":1,"end":140527596,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527596,"clinical_significance":[],"id":"rs1796110316","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1003401408","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527600,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140527600},{"seq_region_name":"7","id":"rs1563118472","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527601,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140527601},{"seq_region_name":"7","id":"rs1585554705","clinical_significance":[],"alleles":["C","T"],"end":140527603,"strand":1,"feature_type":"variation","start":140527603,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs182475966","source":"dbSNP","start":140527604,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140527604,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527605,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140527605,"clinical_significance":[],"seq_region_name":"7","id":"rs1279979363"},{"feature_type":"variation","strand":1,"end":140527608,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527608,"clinical_significance":[],"seq_region_name":"7","id":"rs1796111258"},{"seq_region_name":"7","id":"rs1225848351","clinical_significance":[],"start":140527610,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140527610,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1585554744","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527612,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140527612},{"id":"rs1325119640","seq_region_name":"7","clinical_significance":[],"end":140527616,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140527616,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140527617,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140527617,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1167526603","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140527618,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527618,"clinical_significance":[],"seq_region_name":"7","id":"rs958885934"},{"source":"dbSNP","start":140527621,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140527621,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1362233676"},{"feature_type":"variation","strand":1,"end":140527622,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527622,"clinical_significance":[],"seq_region_name":"7","id":"rs1796112454"},{"id":"rs1290208684","seq_region_name":"7","clinical_significance":[],"end":140527631,"alleles":["GAGCACATGA","GA"],"strand":1,"feature_type":"variation","start":140527622,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140527626,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527626,"source":"dbSNP","seq_region_name":"7","id":"rs1016900295","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527631,"feature_type":"variation","strand":1,"end":140527631,"alleles":["A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs963118334"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140527632,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527632,"source":"dbSNP","id":"rs1796112962","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527634,"feature_type":"variation","strand":1,"end":140527634,"alleles":["G","A"],"clinical_significance":[],"id":"rs1796113061","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1428411255","clinical_significance":[],"start":140527638,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140527638,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796113487","end":140527641,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140527641,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527645,"source":"dbSNP","strand":1,"feature_type":"variation","end":140527645,"alleles":["G","A"],"seq_region_name":"7","id":"rs368209592","clinical_significance":[]},{"clinical_significance":[],"id":"rs1796113725","seq_region_name":"7","source":"dbSNP","start":140527646,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140527646,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1016359604","seq_region_name":"7","feature_type":"variation","strand":1,"end":140527647,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527647},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796114043","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140527652,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527652},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796114176","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527654,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140527654},{"alleles":["A","-"],"end":140527662,"feature_type":"variation","strand":1,"source":"dbSNP","start":140527662,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1470905114"},{"strand":1,"feature_type":"variation","end":140527663,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527663,"source":"dbSNP","seq_region_name":"7","id":"rs1174660428","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs962291376","source":"dbSNP","start":140527665,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140527665,"alleles":["G","A","T"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140527666,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140527666,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796114691"},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140527671,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527671,"source":"dbSNP","seq_region_name":"7","id":"rs972304944","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796114860","clinical_significance":[],"alleles":["C","T"],"end":140527672,"strand":1,"feature_type":"variation","start":140527672,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140527673,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527673,"source":"dbSNP","seq_region_name":"7","id":"rs6943131","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs35871682","alleles":["GA","AG"],"end":140527674,"feature_type":"variation","strand":1,"source":"dbSNP","start":140527673,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527674,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140527674,"id":"rs6965644","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1238378933","seq_region_name":"7","end":140527682,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140527682,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1796115475","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527686,"source":"dbSNP","strand":1,"feature_type":"variation","end":140527686,"alleles":["G","A"]},{"id":"rs1206175967","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140527689,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527689,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1460369657","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527694,"source":"dbSNP","strand":1,"feature_type":"variation","end":140527694,"alleles":["A","G"]},{"id":"rs1796115908","seq_region_name":"7","clinical_significance":[],"start":140527696,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140527696,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1796116020","clinical_significance":[],"end":140527698,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140527698,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1796116124","clinical_significance":[],"strand":1,"feature_type":"variation","end":140527705,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527705,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1262995054","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140527711,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527711},{"id":"rs1322991274","seq_region_name":"7","clinical_significance":[],"start":140527714,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140527714,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140527732,"alleles":["T","C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527732,"clinical_significance":[],"seq_region_name":"7","id":"rs1363414186"},{"alleles":["C","T"],"end":140527734,"feature_type":"variation","strand":1,"source":"dbSNP","start":140527734,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1297319988"},{"clinical_significance":[],"seq_region_name":"7","id":"rs987036817","end":140527735,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140527735,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527738,"source":"dbSNP","strand":1,"feature_type":"variation","end":140527744,"alleles":["TCCACAT","T"],"id":"rs1429635589","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140527743,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527743,"clinical_significance":[],"seq_region_name":"7","id":"rs1796117119"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140527746,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527746,"clinical_significance":[],"id":"rs1361077040","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527749,"source":"dbSNP","strand":1,"feature_type":"variation","end":140527749,"alleles":["G","A"],"seq_region_name":"7","id":"rs911493170","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796117461","source":"dbSNP","start":140527751,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140527751,"feature_type":"variation","strand":1},{"start":140527752,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140527752,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1315459290","clinical_significance":[]},{"seq_region_name":"7","id":"rs552701149","clinical_significance":[],"start":140527755,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140527755,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs570897997","source":"dbSNP","start":140527756,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140527756,"alleles":["G","A"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140527760,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527760,"clinical_significance":[],"seq_region_name":"7","id":"rs910956739"},{"id":"rs1796117992","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527763,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140527763},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527768,"source":"dbSNP","strand":1,"feature_type":"variation","end":140527768,"alleles":["C","T"],"id":"rs942937636","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1329801652","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140527769,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527769,"source":"dbSNP"},{"seq_region_name":"7","id":"rs538226071","clinical_significance":[],"strand":1,"feature_type":"variation","end":140527770,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527770,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527771,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C","T"],"end":140527771,"id":"rs914368410","seq_region_name":"7","clinical_significance":[]},{"id":"rs1446194878","seq_region_name":"7","clinical_significance":[],"start":140527773,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140527773,"strand":1,"feature_type":"variation"},{"end":140527774,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140527774,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1185817113","clinical_significance":[]},{"alleles":["T","A"],"end":140527775,"feature_type":"variation","strand":1,"source":"dbSNP","start":140527775,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs879074314"},{"seq_region_name":"7","id":"rs1796119060","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527778,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140527778},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796119220","source":"dbSNP","start":140527780,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140527780,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs536840937","alleles":["TTTTTTT","TTTTTT","TTTTTTTT"],"end":140527786,"feature_type":"variation","strand":1,"source":"dbSNP","start":140527780,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1796119538","seq_region_name":"7","source":"dbSNP","start":140527787,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140527787,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140527788,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527788,"clinical_significance":[],"seq_region_name":"7","id":"rs2130470202"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527789,"source":"dbSNP","strand":1,"feature_type":"variation","end":140527789,"alleles":["G","T"],"id":"rs1796119662","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1179769869","source":"dbSNP","start":140527797,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140527797,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1796119950","clinical_significance":[],"strand":1,"feature_type":"variation","end":140527798,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527798,"source":"dbSNP"},{"alleles":["G","T"],"end":140527807,"strand":1,"feature_type":"variation","start":140527807,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796120087","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796120170","clinical_significance":[],"strand":1,"feature_type":"variation","end":140527819,"alleles":["TTTATTTATT","TTTATT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527810,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140527826,"alleles":["TTATTTATTATTTATT","TTATTTATT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527811,"source":"dbSNP","seq_region_name":"7","id":"rs557268334","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796120372","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527812,"feature_type":"variation","strand":1,"end":140527812,"alleles":["T","A","C"]},{"end":140527815,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140527815,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs924933987"},{"clinical_significance":[],"seq_region_name":"7","id":"rs148220740","source":"dbSNP","start":140527815,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140527822,"alleles":["TTATTATT","TTATT"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140527816,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527816,"clinical_significance":[],"id":"rs1796120707","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527817,"feature_type":"variation","strand":1,"end":140527817,"alleles":["A","T"],"clinical_significance":[],"id":"rs1585555174","seq_region_name":"7"},{"seq_region_name":"7","id":"rs539829097","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527818,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TT","TTT","TTTATTT","TTTATTTATTT"],"end":140527819},{"start":140527818,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140527837,"alleles":["TTATTTATTTATTTATTTAT","TTATTTATTTAT","TTATTTATTTATTTAT","TTATTTATTTATTTATTTATTTAT"],"strand":1,"feature_type":"variation","id":"rs1554459356","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140527820,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140527820,"alleles":["A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs935116436"},{"strand":1,"feature_type":"variation","end":140527821,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527821,"source":"dbSNP","seq_region_name":"7","id":"rs1052177575","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140527825,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527825,"source":"dbSNP","id":"rs1796121378","seq_region_name":"7","clinical_significance":[]},{"start":140527830,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140527830,"alleles":["T","A"],"strand":1,"feature_type":"variation","id":"rs1796121465","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140527831,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140527831,"alleles":["T","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796121553"},{"strand":1,"feature_type":"variation","end":140527836,"alleles":["TTA","TTAGTTA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527834,"source":"dbSNP","seq_region_name":"7","id":"rs1375678922","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130470381","feature_type":"variation","strand":1,"alleles":["A","T"],"end":140527836,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527836},{"source":"dbSNP","start":140527837,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140527837,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1296507125"},{"source":"dbSNP","start":140527838,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140527838,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796121800"},{"id":"rs28472289","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140527845,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527845,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["TTTTTTT","TTTTTT","TTTTTTTT"],"end":140527852,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527846,"source":"dbSNP","id":"rs1055834224","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1366446258","clinical_significance":[],"start":140527847,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140527847,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"alleles":["T","C","G"],"end":140527848,"feature_type":"variation","strand":1,"source":"dbSNP","start":140527848,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1585555296","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140527857,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527857,"clinical_significance":[],"id":"rs894578881","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1400477207","clinical_significance":[],"start":140527858,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140527858,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140527861,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140527861,"alleles":["G","A","C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1006240268"},{"clinical_significance":[],"id":"rs1421386681","seq_region_name":"7","feature_type":"variation","strand":1,"end":140527865,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527865},{"source":"dbSNP","start":140527869,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140527869,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1796122498","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1796122591","clinical_significance":[],"strand":1,"feature_type":"variation","end":140527871,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527871,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796122673","alleles":["G","A"],"end":140527874,"feature_type":"variation","strand":1,"source":"dbSNP","start":140527874,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","T"],"end":140527875,"strand":1,"feature_type":"variation","start":140527875,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1563118630","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796122830","clinical_significance":[],"end":140527877,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140527877,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1248063326","clinical_significance":[],"alleles":["G","A"],"end":140527879,"strand":1,"feature_type":"variation","start":140527879,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140527880,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140527880,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1252135369"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140527884,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527884,"clinical_significance":[],"seq_region_name":"7","id":"rs1796123075"},{"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140527885,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527885,"source":"dbSNP","id":"rs896350935","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796123274","feature_type":"variation","strand":1,"end":140527888,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527888},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527890,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140527890,"seq_region_name":"7","id":"rs1332467131","clinical_significance":[]},{"seq_region_name":"7","id":"rs1482407970","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527895,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140527895},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527896,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140527896,"clinical_significance":[],"seq_region_name":"7","id":"rs1433794918"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796123624","source":"dbSNP","start":140527904,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140527904,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs754184875","feature_type":"variation","strand":1,"alleles":["C","A","G"],"end":140527906,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527906},{"id":"rs207468670","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140527907,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527907,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527908,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140527908,"seq_region_name":"7","id":"rs1796123890","clinical_significance":[]},{"seq_region_name":"7","id":"rs1282127974","clinical_significance":[],"strand":1,"feature_type":"variation","end":140527909,"alleles":["A","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527909,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1290730658","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140527914,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527914},{"seq_region_name":"7","id":"rs1796124058","clinical_significance":[],"strand":1,"feature_type":"variation","end":140527917,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527917,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1796124129","clinical_significance":[],"start":140527924,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140527924,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527926,"source":"dbSNP","strand":1,"feature_type":"variation","end":140527926,"alleles":["C","A"],"seq_region_name":"7","id":"rs1796124211","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585555495","clinical_significance":[],"strand":1,"feature_type":"variation","end":140527927,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527927,"source":"dbSNP"},{"id":"rs1350534773","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527927,"source":"dbSNP","strand":1,"feature_type":"variation","end":140527928,"alleles":["CA","-"]},{"id":"rs1230205185","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140527929,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527929,"source":"dbSNP"},{"alleles":["A","C"],"end":140527934,"strand":1,"feature_type":"variation","start":140527934,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796124579","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796124660","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140527936,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527936},{"strand":1,"feature_type":"variation","end":140527937,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527937,"source":"dbSNP","seq_region_name":"7","id":"rs1796124744","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527941,"feature_type":"variation","strand":1,"end":140527941,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130470706"},{"alleles":["A","C"],"end":140527944,"strand":1,"feature_type":"variation","start":140527944,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs2130470716","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1304710810","feature_type":"variation","strand":1,"end":140527945,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527945},{"id":"rs1266157125","seq_region_name":"7","clinical_significance":[],"end":140527952,"alleles":["CCC","CC"],"strand":1,"feature_type":"variation","start":140527950,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140527957,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527957,"clinical_significance":[],"seq_region_name":"7","id":"rs1016392392"},{"clinical_significance":[],"seq_region_name":"7","id":"rs897962300","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527958,"feature_type":"variation","strand":1,"end":140527958,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1291691773","clinical_significance":[],"end":140527963,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140527963,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs568840030","alleles":["T","C"],"end":140527965,"feature_type":"variation","strand":1,"source":"dbSNP","start":140527965,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1796125357","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140527968,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527968},{"alleles":["A","G"],"end":140527970,"strand":1,"feature_type":"variation","start":140527970,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1013408459","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527972,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140527972,"clinical_significance":[],"seq_region_name":"7","id":"rs148642297"},{"seq_region_name":"7","id":"rs2130470827","clinical_significance":[],"alleles":["G","A"],"end":140527980,"strand":1,"feature_type":"variation","start":140527980,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527981,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140527981,"seq_region_name":"7","id":"rs757452083","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527983,"source":"dbSNP","strand":1,"feature_type":"variation","end":140527983,"alleles":["G","A"],"seq_region_name":"7","id":"rs1796125744","clinical_significance":[]},{"start":140527984,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140527984,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1403314961","clinical_significance":[]},{"clinical_significance":[],"id":"rs1006095625","seq_region_name":"7","feature_type":"variation","strand":1,"end":140527985,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527985},{"source":"dbSNP","start":140527987,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140527987,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1268315315","seq_region_name":"7"},{"id":"rs1289816778","seq_region_name":"7","clinical_significance":[],"end":140527988,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140527988,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1472944585","source":"dbSNP","start":140527989,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140527989,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs778327396","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527990,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140527990},{"clinical_significance":[],"seq_region_name":"7","id":"rs751939133","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527994,"feature_type":"variation","strand":1,"end":140527994,"alleles":["C","A","T"]},{"feature_type":"variation","strand":1,"end":140527995,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527995,"clinical_significance":[],"id":"rs1796126494","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140527997,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140527997,"source":"dbSNP","seq_region_name":"7","id":"rs1429339705","clinical_significance":[]},{"source":"dbSNP","start":140527998,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140527998,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1470013240"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796126908","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140527999,"feature_type":"variation","strand":1,"end":140527999,"alleles":["C","G","T"]},{"start":140528001,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140528001,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs1796127026","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140528003,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528003,"clinical_significance":[],"seq_region_name":"7","id":"rs1201195029"},{"id":"rs1796127202","seq_region_name":"7","clinical_significance":[],"start":140528007,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140528007,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140528013,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528013,"source":"dbSNP","id":"rs994240472","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130470980","alleles":["C","T"],"end":140528014,"feature_type":"variation","strand":1,"source":"dbSNP","start":140528014,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140528016,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528016,"source":"dbSNP","seq_region_name":"7","id":"rs1796127390","clinical_significance":[]},{"alleles":["A","G"],"end":140528021,"feature_type":"variation","strand":1,"source":"dbSNP","start":140528021,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1025665517"},{"seq_region_name":"7","id":"rs1796127536","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528025,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140528025},{"start":140528026,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140528026,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs955434103","clinical_significance":[]},{"source":"dbSNP","start":140528027,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140528027,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs183336060"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140528029,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528029,"clinical_significance":[],"id":"rs1796127860","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140528030,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528030,"source":"dbSNP","id":"rs1486697352","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1258923641","end":140528031,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140528031,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140528041,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140528041,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1017930499","clinical_significance":[]},{"start":140528051,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140528051,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs963790535","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796128253","clinical_significance":[],"strand":1,"feature_type":"variation","end":140528056,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528056,"source":"dbSNP"},{"id":"rs1796128348","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528058,"source":"dbSNP","strand":1,"feature_type":"variation","end":140528058,"alleles":["C","T"]},{"id":"rs1796128430","seq_region_name":"7","clinical_significance":[],"end":140528059,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140528059,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796128508","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140528066,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528066},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528069,"source":"dbSNP","strand":1,"feature_type":"variation","end":140528069,"alleles":["G","T"],"id":"rs911356967","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1221988119","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140528074,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528074},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528083,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140528083,"seq_region_name":"7","id":"rs539329875","clinical_significance":[]},{"alleles":["G","A"],"end":140528084,"strand":1,"feature_type":"variation","start":140528084,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs535685219","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140528085,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528085,"clinical_significance":[],"seq_region_name":"7","id":"rs1319158508"},{"feature_type":"variation","strand":1,"end":140528086,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528086,"clinical_significance":[],"seq_region_name":"7","id":"rs924975346"},{"end":140528087,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140528087,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs200797167"},{"seq_region_name":"7","id":"rs1796129241","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140528092,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528092,"source":"dbSNP"},{"end":140528093,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140528093,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796129329","clinical_significance":[]},{"end":140528104,"alleles":["AGCCCCTCAAAG","AG"],"strand":1,"feature_type":"variation","start":140528093,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796129419","clinical_significance":[]},{"source":"dbSNP","start":140528096,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140528096,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1796129498","seq_region_name":"7"},{"source":"dbSNP","start":140528100,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140528100,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1796129573","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796129655","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528102,"feature_type":"variation","strand":1,"end":140528102,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs1796129744","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528106,"source":"dbSNP","strand":1,"feature_type":"variation","end":140528106,"alleles":["G","A"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528108,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140528108,"clinical_significance":[],"seq_region_name":"7","id":"rs1796129831"},{"source":"dbSNP","start":140528110,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140528110,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1796129925","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140528115,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528115,"clinical_significance":[],"seq_region_name":"7","id":"rs1796130016"},{"alleles":["CAGGC","CAGGCAGGC"],"end":140528120,"feature_type":"variation","strand":1,"source":"dbSNP","start":140528116,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1796130090","seq_region_name":"7"},{"alleles":["C","T"],"end":140528120,"strand":1,"feature_type":"variation","start":140528120,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs935001076","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528121,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140528121,"clinical_significance":[],"id":"rs1370702299","seq_region_name":"7"},{"id":"rs115041851","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528122,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140528122},{"alleles":["G","A"],"end":140528125,"strand":1,"feature_type":"variation","start":140528125,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1406245578","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140528126,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528126,"clinical_significance":[],"seq_region_name":"7","id":"rs746300886"},{"seq_region_name":"7","id":"rs572857991","clinical_significance":[],"start":140528131,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140528131,"strand":1,"feature_type":"variation"},{"start":140528134,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140528134,"alleles":["C","A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1245360076","clinical_significance":[]},{"alleles":["G","A"],"end":140528137,"strand":1,"feature_type":"variation","start":140528137,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1796130992","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528138,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140528138,"seq_region_name":"7","id":"rs1796131078","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs928554461","source":"dbSNP","start":140528144,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140528144,"feature_type":"variation","strand":1},{"start":140528145,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140528145,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1285761369","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1208096665","feature_type":"variation","strand":1,"end":140528149,"alleles":["G","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528149},{"clinical_significance":[],"seq_region_name":"7","id":"rs1353951043","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528156,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140528156},{"end":140528159,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140528159,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs540373121"},{"source":"dbSNP","start":140528160,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140528160,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1264858290"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528163,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140528163,"seq_region_name":"7","id":"rs1201870629","clinical_significance":[]},{"source":"dbSNP","start":140528168,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140528168,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1344333137"},{"source":"dbSNP","start":140528170,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140528170,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796131800"},{"id":"rs1796131898","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140528171,"strand":1,"feature_type":"variation","start":140528171,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1796131985","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140528174,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528174},{"id":"rs1271020319","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528175,"source":"dbSNP","strand":1,"feature_type":"variation","end":140528175,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1229841634","clinical_significance":[],"end":140528185,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140528185,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585555943","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140528186,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528186},{"clinical_significance":[],"id":"rs143783439","seq_region_name":"7","end":140528190,"alleles":["CCCCC","CCCC"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140528186,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140528187,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140528187,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1796132539","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs748138916","alleles":["C","G"],"end":140528189,"feature_type":"variation","strand":1,"source":"dbSNP","start":140528189,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796132718","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140528195,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528195},{"clinical_significance":[],"seq_region_name":"7","id":"rs1454045758","feature_type":"variation","strand":1,"alleles":["AAACAAAACAAAA","AAACAAAACAAAACAAAA"],"end":140528208,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528196},{"start":140528199,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140528199,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1385624379","clinical_significance":[]},{"source":"dbSNP","start":140528200,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AAAA","AAA"],"end":140528203,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs564797261"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140528205,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528205,"source":"dbSNP","id":"rs1207387538","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1248435317","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528209,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140528209},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528211,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140528211,"seq_region_name":"7","id":"rs1467803575","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528214,"feature_type":"variation","strand":1,"end":140528214,"alleles":["A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs558223839"},{"feature_type":"variation","strand":1,"end":140528216,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528216,"clinical_significance":[],"seq_region_name":"7","id":"rs942129205"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528217,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140528217,"clinical_significance":[],"seq_region_name":"7","id":"rs1168189089"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528218,"source":"dbSNP","strand":1,"feature_type":"variation","end":140528218,"alleles":["G","T"],"id":"rs1463190985","seq_region_name":"7","clinical_significance":[]},{"id":"rs1796133643","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140528231,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528231,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1370613418","clinical_significance":[],"start":140528233,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140528233,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528237,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140528237,"id":"rs1187707150","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528241,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140528241,"clinical_significance":[],"seq_region_name":"7","id":"rs1796133926"},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140528242,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528242,"source":"dbSNP","seq_region_name":"7","id":"rs1585556063","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585556073","end":140528245,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140528245,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140528249,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528249,"clinical_significance":[],"seq_region_name":"7","id":"rs576467052"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528252,"source":"dbSNP","strand":1,"feature_type":"variation","end":140528252,"alleles":["T","G"],"seq_region_name":"7","id":"rs113796544","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796134379","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528256,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TGAAGATCTGAAGATG","TG"],"end":140528271},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528259,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140528259,"clinical_significance":[],"seq_region_name":"7","id":"rs1037609709"},{"clinical_significance":[],"seq_region_name":"7","id":"rs562466130","source":"dbSNP","start":140528264,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140528264,"alleles":["T","G"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140528270,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528270,"source":"dbSNP","seq_region_name":"7","id":"rs1585556114","clinical_significance":[]},{"id":"rs1796134687","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140528276,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528276,"source":"dbSNP"},{"start":140528278,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140528278,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796134777","clinical_significance":[]},{"seq_region_name":"7","id":"rs1441954253","clinical_significance":[],"start":140528279,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140528279,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528281,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140528281,"clinical_significance":[],"seq_region_name":"7","id":"rs1796134941"},{"seq_region_name":"7","id":"rs373489944","clinical_significance":[],"strand":1,"feature_type":"variation","end":140528285,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528285,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528286,"feature_type":"variation","strand":1,"end":140528286,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs994147587"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1337689578","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528288,"feature_type":"variation","strand":1,"alleles":["TGT","T"],"end":140528290},{"clinical_significance":[],"seq_region_name":"7","id":"rs1274108233","end":140528298,"alleles":["G","C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140528298,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140528301,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528301,"clinical_significance":[],"seq_region_name":"7","id":"rs1247190139"},{"seq_region_name":"7","id":"rs1385387329","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140528306,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528306,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs769886182","feature_type":"variation","strand":1,"end":140528311,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528311},{"clinical_significance":[],"seq_region_name":"7","id":"rs1447919553","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528315,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140528315},{"strand":1,"feature_type":"variation","end":140528317,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528317,"source":"dbSNP","id":"rs773014482","seq_region_name":"7","clinical_significance":[]},{"start":140528318,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140528318,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs6975257","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796136157","feature_type":"variation","strand":1,"end":140528325,"alleles":["A","C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528325},{"source":"dbSNP","start":140528329,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140528329,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1796136276","seq_region_name":"7"},{"source":"dbSNP","start":140528330,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140528330,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796136360"},{"clinical_significance":[],"id":"rs1018898796","seq_region_name":"7","alleles":["C","G"],"end":140528332,"feature_type":"variation","strand":1,"source":"dbSNP","start":140528332,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs964237652","clinical_significance":[],"start":140528342,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140528342,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs890730620","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528346,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140528346},{"seq_region_name":"7","id":"rs1336063196","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140528350,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528350,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528351,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140528351,"seq_region_name":"7","id":"rs1007775064","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140528352,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528352,"source":"dbSNP","id":"rs1425097722","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796137066","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528354,"source":"dbSNP","strand":1,"feature_type":"variation","end":140528354,"alleles":["G","A"]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140528357,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528357,"clinical_significance":[],"seq_region_name":"7","id":"rs1796137170"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796137256","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528361,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140528361},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796137337","alleles":["C","A"],"end":140528362,"feature_type":"variation","strand":1,"source":"dbSNP","start":140528362,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140528364,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140528364,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796137434"},{"clinical_significance":[],"id":"rs770550790","seq_region_name":"7","source":"dbSNP","start":140528366,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140528366,"alleles":["A","C"],"feature_type":"variation","strand":1},{"id":"rs1796137598","seq_region_name":"7","clinical_significance":[],"start":140528374,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140528374,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["GG","G"],"end":140528377,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528376,"source":"dbSNP","seq_region_name":"7","id":"rs1796137705","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140528377,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528377,"clinical_significance":[],"seq_region_name":"7","id":"rs1244968300"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1161644471","source":"dbSNP","start":140528378,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TACT","TACTACT"],"end":140528381,"feature_type":"variation","strand":1},{"end":140528385,"alleles":["CACA","CA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140528382,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1297973572"},{"alleles":["G","A","C"],"end":140528387,"feature_type":"variation","strand":1,"source":"dbSNP","start":140528387,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs773942455"},{"alleles":["C","G","T"],"end":140528392,"strand":1,"feature_type":"variation","start":140528392,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs6963099","clinical_significance":[]},{"alleles":["A","T"],"end":140528393,"strand":1,"feature_type":"variation","start":140528393,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796138251","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130472029","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528394,"feature_type":"variation","strand":1,"end":140528394,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796138332","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528398,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140528398},{"seq_region_name":"7","id":"rs1249731310","clinical_significance":[],"start":140528401,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","T"],"end":140528401,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140528406,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528406,"source":"dbSNP","id":"rs1201591187","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796138617","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528407,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140528407},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796138700","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528408,"feature_type":"variation","strand":1,"end":140528408,"alleles":["G","C"]},{"end":140528413,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140528413,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1796138788","seq_region_name":"7"},{"source":"dbSNP","start":140528414,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140528414,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796138864"},{"alleles":["G","A"],"end":140528421,"strand":1,"feature_type":"variation","start":140528421,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1436093989","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1258870796","feature_type":"variation","strand":1,"end":140528427,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528427},{"seq_region_name":"7","id":"rs956921378","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140528428,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528428,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1796139199","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528430,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CAGTTGAGCCTTACCCAG","CAG"],"end":140528447},{"end":140528432,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140528432,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796139302","clinical_significance":[]},{"source":"dbSNP","start":140528437,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140528437,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs560342439"},{"id":"rs1011367949","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140528438,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528438,"source":"dbSNP"},{"alleles":["TT","T"],"end":140528441,"strand":1,"feature_type":"variation","start":140528440,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1183385374","clinical_significance":[]},{"source":"dbSNP","start":140528444,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140528444,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796139572"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528448,"source":"dbSNP","strand":1,"feature_type":"variation","end":140528448,"alleles":["A","C"],"seq_region_name":"7","id":"rs1228322808","clinical_significance":[]},{"clinical_significance":[],"id":"rs1796139730","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140528451,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528451},{"clinical_significance":[],"seq_region_name":"7","id":"rs767065227","feature_type":"variation","strand":1,"end":140528454,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528454},{"seq_region_name":"7","id":"rs1796139888","clinical_significance":[],"strand":1,"feature_type":"variation","end":140528459,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528459,"source":"dbSNP"},{"alleles":["G","T"],"end":140528464,"strand":1,"feature_type":"variation","start":140528464,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1281726640","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140528467,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528467,"clinical_significance":[],"seq_region_name":"7","id":"rs987821660"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563118944","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528468,"feature_type":"variation","strand":1,"end":140528468,"alleles":["T","C"]},{"clinical_significance":[],"id":"rs1796140233","seq_region_name":"7","source":"dbSNP","start":140528469,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140528469,"alleles":["G","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs374966623","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528473,"source":"dbSNP","strand":1,"feature_type":"variation","end":140528473,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796140403","source":"dbSNP","start":140528474,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140528474,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1307064673","seq_region_name":"7","feature_type":"variation","strand":1,"end":140528475,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528475},{"source":"dbSNP","start":140528476,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140528476,"alleles":["A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1405151685"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528477,"source":"dbSNP","strand":1,"feature_type":"variation","end":140528477,"alleles":["T","C"],"seq_region_name":"7","id":"rs2130472285","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130472294","feature_type":"variation","strand":1,"end":140528482,"alleles":["TG","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528481},{"start":140528485,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140528485,"strand":1,"feature_type":"variation","id":"rs1796140564","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs917546998","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140528491,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528491},{"source":"dbSNP","start":140528492,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140528492,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs949152129"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528496,"feature_type":"variation","strand":1,"end":140528496,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130472316"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528497,"feature_type":"variation","strand":1,"end":140528497,"alleles":["C","T"],"clinical_significance":[],"id":"rs1404804579","seq_region_name":"7"},{"seq_region_name":"7","id":"rs192928709","clinical_significance":[],"end":140528498,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140528498,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1585556537","clinical_significance":[],"start":140528500,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140528500,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130472348","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528503,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140528503},{"clinical_significance":[],"id":"rs1796141105","seq_region_name":"7","end":140528505,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140528505,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1466090918","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140528507,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528507},{"seq_region_name":"7","id":"rs1411303845","clinical_significance":[],"strand":1,"feature_type":"variation","end":140528508,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528508,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796141378","feature_type":"variation","strand":1,"end":140528509,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528509},{"seq_region_name":"7","id":"rs1796141464","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528514,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140528514},{"end":140528515,"alleles":["AA","AAA"],"strand":1,"feature_type":"variation","start":140528514,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1174313479","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528515,"source":"dbSNP","strand":1,"feature_type":"variation","end":140528515,"alleles":["A","G"],"id":"rs1403821524","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796141711","source":"dbSNP","start":140528518,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140528518,"feature_type":"variation","strand":1},{"id":"rs1266962049","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528519,"source":"dbSNP","strand":1,"feature_type":"variation","end":140528543,"alleles":["CAGCACTTTGGGAGGCCGAGGTGAG","CAGCACTTTGGGAGGCCGAGGTGAGCAGCACTTTGGGAGGCCGAGGTGAG"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528530,"feature_type":"variation","strand":1,"end":140528530,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1796141891"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528535,"source":"dbSNP","strand":1,"feature_type":"variation","end":140528535,"alleles":["C","G","T"],"seq_region_name":"7","id":"rs1451755638","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796142092","clinical_significance":[],"end":140528536,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140528536,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140528538,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140528538,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1221317277"},{"start":140528540,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140528540,"alleles":["T","C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585556589","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796142378","feature_type":"variation","strand":1,"end":140528541,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528541},{"id":"rs1351712537","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140528556,"alleles":["GAGTGGATCACCTGAG","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528541,"source":"dbSNP"},{"end":140528542,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140528542,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1796142565","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140528551,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140528551,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796142652"},{"start":140528554,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140528554,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs1796142742","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs926476618","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528556,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140528556},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140528562,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528562,"source":"dbSNP","seq_region_name":"7","id":"rs2130472524","clinical_significance":[]},{"seq_region_name":"7","id":"rs185519345","clinical_significance":[],"start":140528567,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G","T"],"end":140528567,"strand":1,"feature_type":"variation"},{"start":140528568,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140528568,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs552737916","clinical_significance":[]},{"end":140528572,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140528572,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1796143111","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528575,"feature_type":"variation","strand":1,"end":140528575,"alleles":["G","T"],"clinical_significance":[],"id":"rs1321003635","seq_region_name":"7"},{"seq_region_name":"7","id":"rs897754711","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528576,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140528576},{"clinical_significance":[],"id":"rs1585556647","seq_region_name":"7","end":140528580,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140528580,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140528582,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C","G"],"end":140528582,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1384183449"},{"seq_region_name":"7","id":"rs929190546","clinical_significance":[],"strand":1,"feature_type":"variation","end":140528585,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528585,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140528587,"alleles":["CAT","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528585,"source":"dbSNP","id":"rs1293688689","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1287140443","clinical_significance":[],"end":140528586,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140528586,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs2130472632","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528589,"source":"dbSNP","strand":1,"feature_type":"variation","end":140528589,"alleles":["G","T"]},{"feature_type":"variation","strand":1,"alleles":["AAA","AA"],"end":140528594,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528592,"clinical_significance":[],"seq_region_name":"7","id":"rs1796143851"},{"seq_region_name":"7","id":"rs2130472650","clinical_significance":[],"start":140528595,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140528596,"alleles":["TT","-"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140528595,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TTCCGT","-"],"end":140528600,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796143943"},{"end":140528596,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140528596,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796144013"},{"start":140528598,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140528598,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1307061206","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796144199","clinical_significance":[],"start":140528599,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140528599,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528603,"feature_type":"variation","strand":1,"end":140528602,"alleles":["-","AAA"],"clinical_significance":[],"seq_region_name":"7","id":"rs1796144298"},{"clinical_significance":[],"id":"rs1796144383","seq_region_name":"7","source":"dbSNP","start":140528604,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140528604,"feature_type":"variation","strand":1},{"alleles":["A","G"],"end":140528605,"feature_type":"variation","strand":1,"source":"dbSNP","start":140528605,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1347009814"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528606,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140528606,"clinical_significance":[],"seq_region_name":"7","id":"rs1272657835"},{"start":140528608,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140528608,"strand":1,"feature_type":"variation","id":"rs1047053217","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796144719","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140528609,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528609},{"seq_region_name":"7","id":"rs891124690","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140528612,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528612,"source":"dbSNP"},{"start":140528613,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140528613,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1345535399","clinical_significance":[]},{"alleles":["C","G"],"end":140528615,"feature_type":"variation","strand":1,"source":"dbSNP","start":140528615,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1796144954","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1257780043","source":"dbSNP","start":140528629,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140528629,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs2130472773","clinical_significance":[],"start":140528630,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140528630,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140528632,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528632,"clinical_significance":[],"seq_region_name":"7","id":"rs1455566718"},{"start":140528637,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140528637,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796145230","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1008301676","alleles":["C","G","T"],"end":140528640,"feature_type":"variation","strand":1,"source":"dbSNP","start":140528640,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1018348603","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528641,"source":"dbSNP","strand":1,"feature_type":"variation","end":140528641,"alleles":["G","A","C"]},{"start":140528645,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140528645,"alleles":["A","T"],"strand":1,"feature_type":"variation","id":"rs1427494854","seq_region_name":"7","clinical_significance":[]},{"start":140528647,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140528647,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796145640","clinical_significance":[]},{"seq_region_name":"7","id":"rs1190793156","clinical_significance":[],"start":140528650,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140528650,"strand":1,"feature_type":"variation"},{"alleles":["C","G","T"],"end":140528652,"strand":1,"feature_type":"variation","start":140528652,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs900024300","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1796145927","seq_region_name":"7","end":140528653,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140528653,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1796146015","seq_region_name":"7","clinical_significance":[],"alleles":["G","T"],"end":140528658,"strand":1,"feature_type":"variation","start":140528658,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs565514613","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528659,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140528659},{"feature_type":"variation","strand":1,"end":140528668,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528668,"clinical_significance":[],"id":"rs1796146219","seq_region_name":"7"},{"start":140528670,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140528670,"strand":1,"feature_type":"variation","id":"rs1796146317","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1466510337","clinical_significance":[],"start":140528674,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140528674,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528675,"source":"dbSNP","strand":1,"feature_type":"variation","end":140528675,"alleles":["G","A","C"],"seq_region_name":"7","id":"rs536191809","clinical_significance":[]},{"seq_region_name":"7","id":"rs6948434","clinical_significance":[],"end":140528676,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140528676,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528677,"feature_type":"variation","strand":1,"end":140528677,"alleles":["T","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs959989162"},{"alleles":["G","A"],"end":140528679,"strand":1,"feature_type":"variation","start":140528679,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs370796133","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796146956","source":"dbSNP","start":140528680,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140528680,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528682,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140528682,"id":"rs1276103500","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140528689,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528689,"source":"dbSNP","id":"rs915948624","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140528690,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528690,"clinical_significance":[],"seq_region_name":"7","id":"rs1666475059"},{"seq_region_name":"7","id":"rs1585556900","clinical_significance":[],"alleles":["T","C","G"],"end":140528691,"strand":1,"feature_type":"variation","start":140528691,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140528693,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140528693,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796147307","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528695,"source":"dbSNP","strand":1,"feature_type":"variation","end":140528695,"alleles":["G","A","T"],"seq_region_name":"7","id":"rs942034095","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130473001","alleles":["A","G"],"end":140528706,"feature_type":"variation","strand":1,"source":"dbSNP","start":140528706,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1426528486","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140528708,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528708,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796147620","source":"dbSNP","start":140528712,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140528712,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140528713,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528713,"clinical_significance":[],"seq_region_name":"7","id":"rs1796147707"},{"seq_region_name":"7","id":"rs1271712244","clinical_significance":[],"strand":1,"feature_type":"variation","end":140528714,"alleles":["TT","TTT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528713,"source":"dbSNP"},{"seq_region_name":"7","id":"rs2130473060","clinical_significance":[],"end":140528715,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140528715,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1796147899","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528717,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140528717},{"source":"dbSNP","start":140528719,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140528719,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796147991"},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140528725,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528725,"source":"dbSNP","id":"rs1585556944","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796148222","feature_type":"variation","strand":1,"end":140528726,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528726},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528727,"feature_type":"variation","strand":1,"end":140528727,"alleles":["T","C"],"clinical_significance":[],"id":"rs901689401","seq_region_name":"7"},{"alleles":["T","C"],"end":140528734,"strand":1,"feature_type":"variation","start":140528734,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1037774237","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140528737,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528737,"source":"dbSNP","seq_region_name":"7","id":"rs146728132","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140528738,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528738,"clinical_significance":[],"seq_region_name":"7","id":"rs1390637480"},{"seq_region_name":"7","id":"rs1796149022","clinical_significance":[],"start":140528741,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140528741,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528742,"source":"dbSNP","strand":1,"feature_type":"variation","end":140528742,"alleles":["A","G"],"seq_region_name":"7","id":"rs1288004901","clinical_significance":[]},{"seq_region_name":"7","id":"rs569724079","clinical_significance":[],"end":140528743,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140528743,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs997323719","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140528744,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528744,"source":"dbSNP"},{"end":140528750,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140528750,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs140394615","clinical_significance":[]},{"seq_region_name":"7","id":"rs1028819932","clinical_significance":[],"start":140528753,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140528753,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140528755,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140528755,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1796149824","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528756,"feature_type":"variation","strand":1,"end":140528756,"alleles":["A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1796149950"},{"seq_region_name":"7","id":"rs1285313512","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528758,"source":"dbSNP","strand":1,"feature_type":"variation","end":140528758,"alleles":["C","T"]},{"clinical_significance":[],"id":"rs1343681746","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140528759,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528759},{"feature_type":"variation","strand":1,"alleles":["-","A"],"end":140528759,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528760,"clinical_significance":[],"seq_region_name":"7","id":"rs1796150403"},{"id":"rs1389624849","seq_region_name":"7","clinical_significance":[],"start":140528760,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140528760,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796150678","source":"dbSNP","start":140528760,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140528760,"alleles":["C","-"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1223489247","clinical_significance":[],"strand":1,"feature_type":"variation","end":140528761,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528761,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528761,"feature_type":"variation","strand":1,"alleles":["AAAAAAAAAAAAAA","AAAAAAAAAAAA","AAAAAAAAAAAAA","AAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAA"],"end":140528774,"clinical_significance":[],"seq_region_name":"7","id":"rs555432046"},{"seq_region_name":"7","id":"rs1796151428","clinical_significance":[],"alleles":["A","T"],"end":140528767,"strand":1,"feature_type":"variation","start":140528767,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1449181572","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528768,"feature_type":"variation","strand":1,"end":140528768,"alleles":["A","G"]},{"end":140528776,"alleles":["AAAGA","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140528772,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1796151708","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1244316113","clinical_significance":[],"strand":1,"feature_type":"variation","end":140528775,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528775,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["T","A","G"],"end":140528779,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528779,"clinical_significance":[],"seq_region_name":"7","id":"rs1214094569"},{"id":"rs144173657","seq_region_name":"7","clinical_significance":[],"end":140528783,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","start":140528783,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140528784,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528784,"clinical_significance":[],"id":"rs1462305980","seq_region_name":"7"},{"source":"dbSNP","start":140528787,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140528787,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs890584839","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585557194","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140528789,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528789},{"end":140528790,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140528790,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1209073510","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130473376","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140528795,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528795},{"seq_region_name":"7","id":"rs1796152607","clinical_significance":[],"start":140528796,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140528796,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"id":"rs2130473392","seq_region_name":"7","clinical_significance":[],"start":140528801,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140528801,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"id":"rs6976066","seq_region_name":"7","clinical_significance":[],"start":140528805,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140528805,"strand":1,"feature_type":"variation"},{"end":140528810,"alleles":["A","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140528810,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs970366638"},{"end":140528816,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140528816,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs151030367","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585557241","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528819,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140528819},{"clinical_significance":[],"seq_region_name":"7","id":"rs1315698853","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528820,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140528820},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140528823,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528823,"source":"dbSNP","seq_region_name":"7","id":"rs1796153481","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796153647","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528824,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140528824},{"seq_region_name":"7","id":"rs1796153796","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140528827,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528827,"source":"dbSNP"},{"start":140528829,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140528829,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1479816941","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796154062","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528830,"feature_type":"variation","strand":1,"end":140528830,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1796154196","clinical_significance":[],"start":140528831,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140528831,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs764531113","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140528838,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528838,"source":"dbSNP"},{"start":140528839,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140528839,"alleles":["C","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796154510","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796154632","clinical_significance":[],"start":140528843,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140528843,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528845,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140528845,"seq_region_name":"7","id":"rs1302327292","clinical_significance":[]},{"clinical_significance":[],"id":"rs1442931726","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528848,"feature_type":"variation","strand":1,"alleles":["GTG","GTGTG"],"end":140528850},{"feature_type":"variation","strand":1,"alleles":["TGACTGATG","TG"],"end":140528857,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528849,"clinical_significance":[],"id":"rs1796154989","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140528854,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528854,"clinical_significance":[],"seq_region_name":"7","id":"rs1356504716"},{"seq_region_name":"7","id":"rs967174415","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528855,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140528855},{"end":140528856,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140528856,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1429547418","clinical_significance":[]},{"seq_region_name":"7","id":"rs754169913","clinical_significance":[],"strand":1,"feature_type":"variation","end":140528871,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528871,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1796155408","seq_region_name":"7","source":"dbSNP","start":140528875,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140528875,"alleles":["T","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1796155524","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528879,"source":"dbSNP","strand":1,"feature_type":"variation","end":140528896,"alleles":["GAGGCTGAGGTGGTCAGA","GA"]},{"alleles":["G","C"],"end":140528882,"strand":1,"feature_type":"variation","start":140528882,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs6948774","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528884,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140528884,"seq_region_name":"7","id":"rs919045624","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1422578772","source":"dbSNP","start":140528886,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140528886,"alleles":["A","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796156091","alleles":["G","A"],"end":140528887,"feature_type":"variation","strand":1,"source":"dbSNP","start":140528887,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140528888,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140528888,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs929265430","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","G"],"end":140528892,"strand":1,"feature_type":"variation","start":140528892,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796156350","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528893,"source":"dbSNP","strand":1,"feature_type":"variation","end":140528893,"alleles":["C","G"],"seq_region_name":"7","id":"rs1796156482","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140528897,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528897,"clinical_significance":[],"seq_region_name":"7","id":"rs959860727"},{"alleles":["G","A"],"end":140528898,"strand":1,"feature_type":"variation","start":140528898,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796156759","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140528900,"alleles":["T","C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528900,"clinical_significance":[],"id":"rs1585557359","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140528904,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528904,"clinical_significance":[],"seq_region_name":"7","id":"rs1480646909"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140528907,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528907,"source":"dbSNP","seq_region_name":"7","id":"rs1796157180","clinical_significance":[]},{"alleles":["G","A"],"end":140528909,"strand":1,"feature_type":"variation","start":140528909,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796157311","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528914,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140528914,"clinical_significance":[],"seq_region_name":"7","id":"rs1796157439"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796157556","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140528916,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528916},{"seq_region_name":"7","id":"rs1234289809","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528920,"source":"dbSNP","strand":1,"feature_type":"variation","end":140528920,"alleles":["A","G"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528923,"source":"dbSNP","strand":1,"feature_type":"variation","end":140528923,"alleles":["G","A"],"seq_region_name":"7","id":"rs1350216504","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796157954","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528926,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140528926},{"feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140528927,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528927,"clinical_significance":[],"seq_region_name":"7","id":"rs6980049"},{"seq_region_name":"7","id":"rs750666751","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528929,"source":"dbSNP","strand":1,"feature_type":"variation","end":140528929,"alleles":["C","A","T"]},{"strand":1,"feature_type":"variation","end":140528930,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528930,"source":"dbSNP","seq_region_name":"7","id":"rs1248164481","clinical_significance":[]},{"seq_region_name":"7","id":"rs6975258","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528933,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140528933},{"seq_region_name":"7","id":"rs1796158814","clinical_significance":[],"start":140528935,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140528935,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"id":"rs1311844256","seq_region_name":"7","clinical_significance":[],"start":140528938,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140528938,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1796159081","clinical_significance":[],"end":140528939,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140528939,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528941,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140528941,"seq_region_name":"7","id":"rs1796159255","clinical_significance":[]},{"seq_region_name":"7","id":"rs1224426487","clinical_significance":[],"end":140528949,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140528949,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1375572409","seq_region_name":"7","clinical_significance":[],"end":140528950,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140528950,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796159500","feature_type":"variation","strand":1,"alleles":["AAAAA","AAAAAA"],"end":140528955,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528951},{"id":"rs1796159605","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528954,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140528954},{"end":140528958,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140528958,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs537464684"},{"id":"rs555701028","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528959,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140528959},{"source":"dbSNP","start":140528961,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C","G"],"end":140528961,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1306448013"},{"start":140528973,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140528973,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1404405274","clinical_significance":[]},{"seq_region_name":"7","id":"rs1291351591","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528977,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140528977},{"start":140528978,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140528978,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs553340166","clinical_significance":[]},{"start":140528979,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140528979,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796160296","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140528982,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140528982,"clinical_significance":[],"id":"rs1585557544","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1305346303","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140528988,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140528988},{"clinical_significance":[],"id":"rs1376181488","seq_region_name":"7","alleles":["G","A"],"end":140528991,"feature_type":"variation","strand":1,"source":"dbSNP","start":140528991,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796160842","alleles":["T","C","G"],"end":140528997,"feature_type":"variation","strand":1,"source":"dbSNP","start":140528997,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs574647672","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140529001,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529001},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796161123","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529004,"feature_type":"variation","strand":1,"end":140529004,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs542147843","clinical_significance":[],"strand":1,"feature_type":"variation","end":140529006,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529006,"source":"dbSNP"},{"alleles":["G","A"],"end":140529008,"strand":1,"feature_type":"variation","start":140529008,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796161386","clinical_significance":[]},{"seq_region_name":"7","id":"rs973443269","clinical_significance":[],"end":140529012,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140529012,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1222514510","source":"dbSNP","start":140529013,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140529013,"alleles":["G","A"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529017,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140529017,"seq_region_name":"7","id":"rs899929383","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140529018,"alleles":["C","A","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529018,"clinical_significance":[],"seq_region_name":"7","id":"rs1001325385"},{"end":140529019,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140529019,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796162178","clinical_significance":[]},{"id":"rs1796162310","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140529036,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529036,"source":"dbSNP"},{"source":"dbSNP","start":140529037,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140529037,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1322664101","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1269065854","seq_region_name":"7","alleles":["G","A"],"end":140529040,"feature_type":"variation","strand":1,"source":"dbSNP","start":140529040,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1472055500","clinical_significance":[],"start":140529040,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140529041,"alleles":["GG","G"],"strand":1,"feature_type":"variation"},{"id":"rs866373656","seq_region_name":"7","clinical_significance":[],"alleles":["G","T"],"end":140529041,"strand":1,"feature_type":"variation","start":140529041,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1585557649","clinical_significance":[],"end":140529042,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140529042,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1247790339","clinical_significance":[],"end":140529045,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140529045,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529046,"feature_type":"variation","strand":1,"end":140529046,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1796163102"},{"clinical_significance":[],"id":"rs1796163236","seq_region_name":"7","source":"dbSNP","start":140529048,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140529048,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529049,"source":"dbSNP","strand":1,"feature_type":"variation","end":140529056,"alleles":["GAGCCGAG","GAGCCGAGCCGAG"],"id":"rs1289136436","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130474087","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529051,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140529051},{"alleles":["C","A","T"],"end":140529053,"feature_type":"variation","strand":1,"source":"dbSNP","start":140529053,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1487353857","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140529054,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529054,"source":"dbSNP","seq_region_name":"7","id":"rs575078927","clinical_significance":[]},{"clinical_significance":[],"id":"rs1796163658","seq_region_name":"7","source":"dbSNP","start":140529059,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140529059,"alleles":["T","C","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1205273126","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529060,"source":"dbSNP","strand":1,"feature_type":"variation","end":140529060,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1207646815","clinical_significance":[],"strand":1,"feature_type":"variation","end":140529061,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529061,"source":"dbSNP"},{"clinical_significance":[],"id":"rs892629253","seq_region_name":"7","feature_type":"variation","strand":1,"end":140529062,"alleles":["G","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529062},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140529063,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529063,"source":"dbSNP","seq_region_name":"7","id":"rs368934403","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1176524304","source":"dbSNP","start":140529065,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140529065,"alleles":["A","G"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529066,"feature_type":"variation","strand":1,"end":140529066,"alleles":["T","C"],"clinical_significance":[],"id":"rs1286526683","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1796164467","clinical_significance":[],"start":140529069,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140529069,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1585557762","seq_region_name":"7","alleles":["A","C"],"end":140529070,"feature_type":"variation","strand":1,"source":"dbSNP","start":140529070,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140529074,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140529074,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1796164746","seq_region_name":"7"},{"seq_region_name":"7","id":"rs929414720","clinical_significance":[],"alleles":["C","T"],"end":140529077,"strand":1,"feature_type":"variation","start":140529077,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796165056","alleles":["AGAG","AG"],"end":140529090,"feature_type":"variation","strand":1,"source":"dbSNP","start":140529087,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140529089,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140529089,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1346403174","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1052274235","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529090,"feature_type":"variation","strand":1,"end":140529090,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796165463","alleles":["T","C"],"end":140529091,"feature_type":"variation","strand":1,"source":"dbSNP","start":140529091,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140529103,"alleles":["GGCACTGCCT","-"],"strand":1,"feature_type":"variation","start":140529094,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1385485090","clinical_significance":[]},{"seq_region_name":"7","id":"rs189327884","clinical_significance":[],"strand":1,"feature_type":"variation","end":140529095,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529095,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1796165811","clinical_significance":[],"strand":1,"feature_type":"variation","end":140529098,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529098,"source":"dbSNP"},{"seq_region_name":"7","id":"rs912102449","clinical_significance":[],"start":140529100,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140529100,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1796166011","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529101,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140529101},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529104,"source":"dbSNP","strand":1,"feature_type":"variation","end":140529104,"alleles":["C","T"],"id":"rs1455796870","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs943496470","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529106,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140529106},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796166283","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140529107,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529107},{"clinical_significance":[],"seq_region_name":"7","id":"rs1039330295","end":140529108,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140529108,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs894074309","clinical_significance":[],"strand":1,"feature_type":"variation","end":140529109,"alleles":["A","C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529109,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1011138308","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140529110,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529110},{"start":140529111,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140529111,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796166702","clinical_significance":[]},{"clinical_significance":[],"id":"rs1796166794","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140529116,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529116},{"strand":1,"feature_type":"variation","end":140529117,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529117,"source":"dbSNP","id":"rs1796166894","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1042733704","seq_region_name":"7","source":"dbSNP","start":140529122,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C","G"],"end":140529122,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1796167134","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140529124,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529124,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["AAAAAAAA","AAAAAAAAA","AAAAAAAAAA"],"end":140529132,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529125,"clinical_significance":[],"seq_region_name":"7","id":"rs146154358"},{"id":"rs1025211000","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140529129,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529129,"source":"dbSNP"},{"alleles":["A","C","T"],"end":140529132,"strand":1,"feature_type":"variation","start":140529132,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs150196705","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796167607","feature_type":"variation","strand":1,"end":140529133,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529133},{"start":140529135,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140529135,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1563119255","clinical_significance":[]},{"seq_region_name":"7","id":"rs1208213333","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529136,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140529136},{"source":"dbSNP","start":140529141,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140529141,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796167872"},{"feature_type":"variation","strand":1,"end":140529147,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529147,"clinical_significance":[],"seq_region_name":"7","id":"rs1424189715"},{"seq_region_name":"7","id":"rs1796168065","clinical_significance":[],"alleles":["T","C"],"end":140529148,"strand":1,"feature_type":"variation","start":140529148,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130474481","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529149,"feature_type":"variation","strand":1,"end":140529149,"alleles":["G","A"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529150,"source":"dbSNP","strand":1,"feature_type":"variation","end":140529150,"alleles":["G","T"],"seq_region_name":"7","id":"rs1796168145","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796168230","clinical_significance":[],"end":140529166,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140529166,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1796168316","clinical_significance":[],"start":140529167,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140529167,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"id":"rs1265271949","seq_region_name":"7","clinical_significance":[],"start":140529168,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140529168,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1308736877","clinical_significance":[],"end":140529178,"alleles":["AATGGTCAGG","-"],"strand":1,"feature_type":"variation","start":140529169,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140529179,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529179,"clinical_significance":[],"id":"rs1796168580","seq_region_name":"7"},{"start":140529180,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140529180,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1001889289","clinical_significance":[]},{"seq_region_name":"7","id":"rs1035847738","clinical_significance":[],"start":140529185,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140529185,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140529186,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529186,"clinical_significance":[],"seq_region_name":"7","id":"rs752693904"},{"end":140529187,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140529187,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs531796960","clinical_significance":[]},{"seq_region_name":"7","id":"rs1022725713","clinical_significance":[],"start":140529191,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140529191,"strand":1,"feature_type":"variation"},{"alleles":["G","C"],"end":140529194,"feature_type":"variation","strand":1,"source":"dbSNP","start":140529194,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130474567"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1320416589","end":140529195,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140529195,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs973558486","clinical_significance":[],"end":140529196,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140529196,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs763303201","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529197,"feature_type":"variation","strand":1,"end":140529197,"alleles":["G","A","C"]},{"seq_region_name":"7","id":"rs1174018499","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140529201,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529201,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1313301435","source":"dbSNP","start":140529207,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140529207,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140529208,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529208,"source":"dbSNP","seq_region_name":"7","id":"rs764440193","clinical_significance":[]},{"end":140529209,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140529209,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796169811"},{"id":"rs1796169917","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140529217,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529217,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529218,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140529218,"seq_region_name":"7","id":"rs1796170006","clinical_significance":[]},{"source":"dbSNP","start":140529224,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140529224,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs751780107"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529225,"source":"dbSNP","strand":1,"feature_type":"variation","end":140529225,"alleles":["G","A","C","T"],"seq_region_name":"7","id":"rs911828929","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529228,"feature_type":"variation","strand":1,"end":140529228,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1796170343"},{"source":"dbSNP","start":140529233,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140529233,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs191279235"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140529244,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529244,"clinical_significance":[],"id":"rs1246147728","seq_region_name":"7"},{"id":"rs542552146","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529246,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140529246},{"start":140529248,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140529248,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796170791","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529251,"feature_type":"variation","strand":1,"end":140529251,"alleles":["C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130474726"},{"clinical_significance":[],"seq_region_name":"7","id":"rs374836260","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529252,"feature_type":"variation","strand":1,"end":140529252,"alleles":["A","G"]},{"id":"rs529265145","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529254,"source":"dbSNP","strand":1,"feature_type":"variation","end":140529254,"alleles":["T","C"]},{"clinical_significance":[],"id":"rs563927519","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529256,"feature_type":"variation","strand":1,"end":140529256,"alleles":["C","A","T"]},{"seq_region_name":"7","id":"rs936801565","clinical_significance":[],"strand":1,"feature_type":"variation","end":140529257,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529257,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529260,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140529260,"seq_region_name":"7","id":"rs1199011893","clinical_significance":[]},{"alleles":["C","T"],"end":140529261,"feature_type":"variation","strand":1,"source":"dbSNP","start":140529261,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796171346"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140529262,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529262,"clinical_significance":[],"seq_region_name":"7","id":"rs1796171430"},{"seq_region_name":"7","id":"rs1344589722","clinical_significance":[],"start":140529264,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140529264,"strand":1,"feature_type":"variation"},{"end":140529265,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140529265,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796171597"},{"seq_region_name":"7","id":"rs1796171689","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529273,"source":"dbSNP","strand":1,"feature_type":"variation","end":140529273,"alleles":["A","G"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529278,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140529278,"clinical_significance":[],"seq_region_name":"7","id":"rs6942494"},{"start":140529285,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","T"],"end":140529285,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs566221420","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796172171","clinical_significance":[],"start":140529286,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140529286,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140529291,"alleles":["T","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529291,"clinical_significance":[],"seq_region_name":"7","id":"rs1796172245"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1231105976","alleles":["C","G","T"],"end":140529295,"feature_type":"variation","strand":1,"source":"dbSNP","start":140529295,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140529309,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140529309,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796172438","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1340433157","end":140529311,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140529311,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140529312,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529312,"clinical_significance":[],"seq_region_name":"7","id":"rs1796172600"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529322,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140529322,"id":"rs1297566678","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1453967640","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529328,"feature_type":"variation","strand":1,"end":140529328,"alleles":["C","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529330,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140529330,"clinical_significance":[],"seq_region_name":"7","id":"rs1796172833"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796172921","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529337,"feature_type":"variation","strand":1,"end":140529337,"alleles":["A","G"]},{"end":140529338,"alleles":["C","CC"],"strand":1,"feature_type":"variation","start":140529338,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs71520099","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796173095","source":"dbSNP","start":140529339,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140529339,"alleles":["T","C"],"feature_type":"variation","strand":1},{"alleles":["G","A"],"end":140529340,"strand":1,"feature_type":"variation","start":140529340,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585558151","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140529343,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529343,"source":"dbSNP","seq_region_name":"7","id":"rs1796173276","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529344,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140529344,"seq_region_name":"7","id":"rs1382960507","clinical_significance":[]},{"seq_region_name":"7","id":"rs892668844","clinical_significance":[],"alleles":["A","G"],"end":140529346,"strand":1,"feature_type":"variation","start":140529346,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140529351,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529351,"source":"dbSNP","seq_region_name":"7","id":"rs1796173544","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529353,"source":"dbSNP","strand":1,"feature_type":"variation","end":140529353,"alleles":["T","C"],"seq_region_name":"7","id":"rs1009753770","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs539667287","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529355,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140529355},{"seq_region_name":"7","id":"rs1169432338","clinical_significance":[],"strand":1,"feature_type":"variation","end":140529356,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529356,"source":"dbSNP"},{"source":"dbSNP","start":140529358,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140529358,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1421802097","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529361,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140529361,"clinical_significance":[],"seq_region_name":"7","id":"rs551526684"},{"seq_region_name":"7","id":"rs911963443","clinical_significance":[],"start":140529365,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140529365,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs570222728","clinical_significance":[],"start":140529368,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140529368,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140529369,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140529369,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs537500916"},{"seq_region_name":"7","id":"rs974924970","clinical_significance":[],"strand":1,"feature_type":"variation","end":140529372,"alleles":["T","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529372,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140529374,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529374,"clinical_significance":[],"seq_region_name":"7","id":"rs1796174606"},{"seq_region_name":"7","id":"rs1046579092","clinical_significance":[],"start":140529377,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140529377,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs906787113","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140529380,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529380},{"seq_region_name":"7","id":"rs1796174891","clinical_significance":[],"alleles":["G","A"],"end":140529381,"strand":1,"feature_type":"variation","start":140529381,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140529382,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529382,"source":"dbSNP","seq_region_name":"7","id":"rs1796174992","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796175091","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529383,"source":"dbSNP","strand":1,"feature_type":"variation","end":140529383,"alleles":["G","A"]},{"alleles":["C","T"],"end":140529387,"strand":1,"feature_type":"variation","start":140529387,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796175190","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529388,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140529388,"id":"rs1002835985","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529392,"feature_type":"variation","strand":1,"end":140529392,"alleles":["C","T"],"clinical_significance":[],"id":"rs1796175414","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1033385800","alleles":["A","G"],"end":140529397,"feature_type":"variation","strand":1,"source":"dbSNP","start":140529397,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140529399,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529399,"source":"dbSNP","id":"rs1796175618","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140529400,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529400,"clinical_significance":[],"seq_region_name":"7","id":"rs1796175748"},{"seq_region_name":"7","id":"rs946961154","clinical_significance":[],"start":140529401,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140529401,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140529408,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529408,"source":"dbSNP","seq_region_name":"7","id":"rs1382463580","clinical_significance":[]},{"clinical_significance":[],"id":"rs1796176264","seq_region_name":"7","end":140529411,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140529411,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1043027344","clinical_significance":[],"alleles":["T","C"],"end":140529415,"strand":1,"feature_type":"variation","start":140529415,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs963371689","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140529417,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529417,"source":"dbSNP"},{"seq_region_name":"7","id":"rs902890455","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529420,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140529420},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529424,"feature_type":"variation","strand":1,"end":140529424,"alleles":["A","AA"],"clinical_significance":[],"seq_region_name":"7","id":"rs1271553594"},{"start":140529424,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140529424,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1359333226","clinical_significance":[]},{"id":"rs183768953","seq_region_name":"7","clinical_significance":[],"alleles":["C","G","T"],"end":140529425,"strand":1,"feature_type":"variation","start":140529425,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140529427,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529427,"source":"dbSNP","seq_region_name":"7","id":"rs1274353058","clinical_significance":[]},{"source":"dbSNP","start":140529429,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140529429,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796177533"},{"end":140529434,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140529434,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1026005941","clinical_significance":[]},{"seq_region_name":"7","id":"rs1056911812","clinical_significance":[],"start":140529436,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140529436,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1359091780","clinical_significance":[],"strand":1,"feature_type":"variation","end":140529439,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529439,"source":"dbSNP"},{"seq_region_name":"7","id":"rs950441814","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140529442,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529442,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529442,"feature_type":"variation","strand":1,"end":140529448,"alleles":["TGGGTAT","-"],"clinical_significance":[],"seq_region_name":"7","id":"rs1325613758"},{"id":"rs1796178488","seq_region_name":"7","clinical_significance":[],"start":140529445,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140529446,"alleles":["GT","-"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140529449,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140529449,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1201645825"},{"start":140529450,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A","C"],"end":140529450,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs895582992","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796178959","clinical_significance":[],"strand":1,"feature_type":"variation","end":140529452,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529452,"source":"dbSNP"},{"seq_region_name":"7","id":"rs574407472","clinical_significance":[],"alleles":["A","C","G"],"end":140529456,"strand":1,"feature_type":"variation","start":140529456,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529458,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140529458,"clinical_significance":[],"seq_region_name":"7","id":"rs1368544991"},{"clinical_significance":[],"seq_region_name":"7","id":"rs141646458","alleles":["G","A"],"end":140529463,"feature_type":"variation","strand":1,"source":"dbSNP","start":140529463,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796179474","source":"dbSNP","start":140529466,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140529466,"feature_type":"variation","strand":1},{"end":140529468,"alleles":["AT","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140529467,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs768683159"},{"clinical_significance":[],"id":"rs1022760057","seq_region_name":"7","alleles":["A","G"],"end":140529470,"feature_type":"variation","strand":1,"source":"dbSNP","start":140529470,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140529476,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529476,"clinical_significance":[],"seq_region_name":"7","id":"rs1796179921"},{"end":140529478,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","start":140529478,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1194249236","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1244063797","clinical_significance":[],"start":140529484,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140529484,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs911684820","clinical_significance":[],"end":140529486,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140529486,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["G","A"],"end":140529488,"strand":1,"feature_type":"variation","start":140529488,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1472533880","clinical_significance":[]},{"seq_region_name":"7","id":"rs964663895","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140529491,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529491,"source":"dbSNP"},{"id":"rs868633708","seq_region_name":"7","clinical_significance":[],"alleles":["C","A","T"],"end":140529492,"strand":1,"feature_type":"variation","start":140529492,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140529494,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140529494,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs554055691"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1186029280","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529495,"feature_type":"variation","strand":1,"end":140529495,"alleles":["C","A","G","T"]},{"start":140529496,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C"],"end":140529496,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs572334303","clinical_significance":[]},{"id":"rs898995110","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529499,"source":"dbSNP","strand":1,"feature_type":"variation","end":140529499,"alleles":["T","C"]},{"source":"dbSNP","start":140529505,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140529505,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs994804490"},{"seq_region_name":"7","id":"rs1796181352","clinical_significance":[],"end":140529506,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140529506,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140529508,"alleles":["C","A","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140529508,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1430031921"},{"alleles":["C","T"],"end":140529510,"feature_type":"variation","strand":1,"source":"dbSNP","start":140529510,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs546027963"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140529512,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529512,"source":"dbSNP","seq_region_name":"7","id":"rs1288394068","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs564883113","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529519,"feature_type":"variation","strand":1,"end":140529519,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796181885","source":"dbSNP","start":140529521,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140529521,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1796181977","seq_region_name":"7","source":"dbSNP","start":140529522,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140529522,"alleles":["A","G"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140529523,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529523,"source":"dbSNP","seq_region_name":"7","id":"rs749105168","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796182169","clinical_significance":[],"start":140529525,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140529525,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140529527,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529527,"clinical_significance":[],"seq_region_name":"7","id":"rs1355104431"},{"end":140529529,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140529529,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1288420929","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs532137523","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529532,"feature_type":"variation","strand":1,"end":140529532,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1585558602","clinical_significance":[],"strand":1,"feature_type":"variation","end":140529536,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529536,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1796182802","seq_region_name":"7","source":"dbSNP","start":140529537,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140529537,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs576298883","clinical_significance":[],"strand":1,"feature_type":"variation","end":140529541,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529541,"source":"dbSNP"},{"alleles":["G","A"],"end":140529542,"strand":1,"feature_type":"variation","start":140529542,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796182956","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796183121","source":"dbSNP","start":140529550,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140529550,"alleles":["G","C"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140529553,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529553,"clinical_significance":[],"seq_region_name":"7","id":"rs989454462"},{"seq_region_name":"7","id":"rs1796183450","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529555,"source":"dbSNP","strand":1,"feature_type":"variation","end":140529555,"alleles":["T","C"]},{"alleles":["C","G","T"],"end":140529556,"feature_type":"variation","strand":1,"source":"dbSNP","start":140529556,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1018932160"},{"end":140529558,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140529558,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796183804"},{"clinical_significance":[],"id":"rs1796183952","seq_region_name":"7","source":"dbSNP","start":140529559,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140529559,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1796184092","clinical_significance":[],"end":140529561,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140529561,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1436973614","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140529562,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529562,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529563,"feature_type":"variation","strand":1,"end":140529563,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs914006779"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529564,"source":"dbSNP","strand":1,"feature_type":"variation","end":140529564,"alleles":["G","T"],"seq_region_name":"7","id":"rs1796184526","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140529580,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529580,"clinical_significance":[],"id":"rs964791079","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529584,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140529584,"clinical_significance":[],"id":"rs1796184803","seq_region_name":"7"},{"id":"rs1317409567","seq_region_name":"7","clinical_significance":[],"start":140529591,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140529591,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1321564514","source":"dbSNP","start":140529593,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140529593,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529594,"feature_type":"variation","strand":1,"end":140529594,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585558668"},{"seq_region_name":"7","id":"rs945405153","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140529595,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529595,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140529603,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529603,"clinical_significance":[],"id":"rs1385846672","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529606,"source":"dbSNP","strand":1,"feature_type":"variation","end":140529606,"alleles":["T","A","C"],"seq_region_name":"7","id":"rs1796185360","clinical_significance":[]},{"clinical_significance":[],"id":"rs543977386","seq_region_name":"7","end":140529607,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140529607,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["T","C"],"end":140529608,"strand":1,"feature_type":"variation","start":140529608,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585558690","clinical_significance":[]},{"id":"rs1240995160","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529609,"source":"dbSNP","strand":1,"feature_type":"variation","end":140529609,"alleles":["G","C"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529610,"source":"dbSNP","strand":1,"feature_type":"variation","end":140529610,"alleles":["C","T"],"id":"rs866148598","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1429531178","clinical_significance":[],"start":140529612,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140529612,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796185980","source":"dbSNP","start":140529615,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140529615,"alleles":["A","G"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140529616,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529616,"source":"dbSNP","seq_region_name":"7","id":"rs1046609781","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["AAAAAA","AAAAA"],"end":140529622,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529617,"source":"dbSNP","seq_region_name":"7","id":"rs1796186183","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140529626,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529626,"source":"dbSNP","seq_region_name":"7","id":"rs1411544319","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["AGTT","AGTTAGTT"],"end":140529631,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529628,"clinical_significance":[],"seq_region_name":"7","id":"rs1200369904"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529630,"source":"dbSNP","strand":1,"feature_type":"variation","end":140529630,"alleles":["T","C"],"seq_region_name":"7","id":"rs1479236143","clinical_significance":[]},{"seq_region_name":"7","id":"rs906691773","clinical_significance":[],"start":140529633,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140529633,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1245329985","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529634,"feature_type":"variation","strand":1,"end":140529634,"alleles":["T","TGT"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796186968","end":140529635,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140529635,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140529636,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529636,"clinical_significance":[],"seq_region_name":"7","id":"rs562028475"},{"seq_region_name":"7","id":"rs1221662461","clinical_significance":[],"strand":1,"feature_type":"variation","end":140529640,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529640,"source":"dbSNP"},{"id":"rs1270510264","seq_region_name":"7","clinical_significance":[],"end":140529648,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140529648,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140529653,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529653,"source":"dbSNP","seq_region_name":"7","id":"rs1796187441","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529654,"source":"dbSNP","strand":1,"feature_type":"variation","end":140529654,"alleles":["G","T"],"seq_region_name":"7","id":"rs1210083145","clinical_significance":[]},{"seq_region_name":"7","id":"rs915449038","clinical_significance":[],"start":140529668,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140529668,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1796187741","clinical_significance":[],"alleles":["A","G"],"end":140529670,"strand":1,"feature_type":"variation","start":140529670,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529671,"feature_type":"variation","strand":1,"end":140529671,"alleles":["T","C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1796187889"},{"start":140529674,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140529674,"strand":1,"feature_type":"variation","id":"rs1796188072","seq_region_name":"7","clinical_significance":[]},{"id":"rs1563119603","seq_region_name":"7","clinical_significance":[],"end":140529676,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140529676,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1585558850","clinical_significance":[],"start":140529682,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140529682,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529685,"source":"dbSNP","strand":1,"feature_type":"variation","end":140529685,"alleles":["T","C"],"id":"rs946873969","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs529318259","clinical_significance":[],"strand":1,"feature_type":"variation","end":140529686,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529686,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1055766078","alleles":["G","A","C","T"],"end":140529687,"feature_type":"variation","strand":1,"source":"dbSNP","start":140529687,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1435408868","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529688,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","CC"],"end":140529688},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796189227","alleles":["C","T"],"end":140529694,"feature_type":"variation","strand":1,"source":"dbSNP","start":140529694,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs898858613","seq_region_name":"7","source":"dbSNP","start":140529695,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140529695,"alleles":["A","G"],"feature_type":"variation","strand":1},{"alleles":["A","G"],"end":140529696,"feature_type":"variation","strand":1,"source":"dbSNP","start":140529696,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs924175581"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796189601","source":"dbSNP","start":140529697,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140529697,"feature_type":"variation","strand":1},{"id":"rs994922451","seq_region_name":"7","clinical_significance":[],"end":140529700,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140529700,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1796189784","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529702,"source":"dbSNP","strand":1,"feature_type":"variation","end":140529702,"alleles":["C","G"]},{"alleles":["C","T"],"end":140529709,"strand":1,"feature_type":"variation","start":140529709,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1796189861","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140529710,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529710,"source":"dbSNP","id":"rs1796189943","seq_region_name":"7","clinical_significance":[]},{"end":140529711,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140529711,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1796190032","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529712,"feature_type":"variation","strand":1,"end":140529712,"alleles":["A","G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1433038042"},{"start":140529713,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140529713,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs541040232","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs886190071","alleles":["G","A","C"],"end":140529714,"feature_type":"variation","strand":1,"source":"dbSNP","start":140529714,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1215295771","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529717,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140529717},{"clinical_significance":[],"id":"rs1796190554","seq_region_name":"7","source":"dbSNP","start":140529719,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140529719,"feature_type":"variation","strand":1},{"end":140529720,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140529720,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796190651"},{"alleles":["C","T"],"end":140529721,"strand":1,"feature_type":"variation","start":140529721,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1796190751","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529723,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140529723,"clinical_significance":[],"seq_region_name":"7","id":"rs1455727412"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1423241195","feature_type":"variation","strand":1,"end":140529725,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529725},{"seq_region_name":"7","id":"rs547467096","clinical_significance":[],"start":140529726,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140529726,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1796191114","clinical_significance":[],"start":140529728,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140529728,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"alleles":["T","C"],"end":140529735,"feature_type":"variation","strand":1,"source":"dbSNP","start":140529735,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1056744457","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1008564791","clinical_significance":[],"alleles":["G","A","T"],"end":140529743,"strand":1,"feature_type":"variation","start":140529743,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796191419","source":"dbSNP","start":140529744,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140529744,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529750,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140529750,"seq_region_name":"7","id":"rs1018765824","clinical_significance":[]},{"alleles":["C","T"],"end":140529751,"strand":1,"feature_type":"variation","start":140529751,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1187195798","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529752,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140529752,"seq_region_name":"7","id":"rs948505483","clinical_significance":[]},{"start":140529753,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140529753,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1246868416","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1210472967","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529757,"feature_type":"variation","strand":1,"end":140529757,"alleles":["C","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1197965819","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529759,"feature_type":"variation","strand":1,"end":140529759,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796192100","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529762,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140529762},{"feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140529764,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529764,"clinical_significance":[],"seq_region_name":"7","id":"rs1313594696"},{"start":140529765,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140529765,"alleles":["G","C"],"strand":1,"feature_type":"variation","id":"rs964885842","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529767,"source":"dbSNP","strand":1,"feature_type":"variation","end":140529767,"alleles":["G","A"],"seq_region_name":"7","id":"rs1796192409","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140529768,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529768,"clinical_significance":[],"id":"rs1796192493","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1342569535","clinical_significance":[],"strand":1,"feature_type":"variation","end":140529770,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529770,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140529774,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529774,"source":"dbSNP","seq_region_name":"7","id":"rs1796192662","clinical_significance":[]},{"source":"dbSNP","start":140529775,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140529775,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs2130476338","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529776,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140529776,"clinical_significance":[],"id":"rs974718626","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796192861","source":"dbSNP","start":140529777,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140529777,"alleles":["A","C"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140529778,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140529778,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796192954"},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140529779,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529779,"clinical_significance":[],"seq_region_name":"7","id":"rs1585559082"},{"feature_type":"variation","strand":1,"end":140529780,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529780,"clinical_significance":[],"seq_region_name":"7","id":"rs113340473"},{"id":"rs371650939","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140529781,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529781,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs779665726","feature_type":"variation","strand":1,"end":140529782,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529782},{"clinical_significance":[],"id":"rs1323781952","seq_region_name":"7","end":140529785,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140529785,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["T","C"],"end":140529791,"feature_type":"variation","strand":1,"source":"dbSNP","start":140529791,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1366960560"},{"end":140529792,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140529792,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1357662401","clinical_significance":[]},{"seq_region_name":"7","id":"rs1402560700","clinical_significance":[],"strand":1,"feature_type":"variation","end":140529793,"alleles":["T","A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529793,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1796193726","clinical_significance":[],"end":140529794,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140529794,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529797,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140529797,"id":"rs989485450","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","G"],"end":140529798,"strand":1,"feature_type":"variation","start":140529798,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1301929415","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs11763530","alleles":["A","C","G","T"],"end":140529799,"feature_type":"variation","strand":1,"source":"dbSNP","start":140529799,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140529801,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140529801,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1241049501"},{"end":140529804,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140529804,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1167329232"},{"seq_region_name":"7","id":"rs1563119685","clinical_significance":[],"start":140529804,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140529805,"alleles":["GA","GAGA"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529806,"feature_type":"variation","strand":1,"end":140529806,"alleles":["C","G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1332666471"},{"id":"rs1386333282","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140529807,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529807,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796194668","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140529808,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529808},{"alleles":["A","-"],"end":140529812,"feature_type":"variation","strand":1,"source":"dbSNP","start":140529812,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1483919144"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140529813,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529813,"clinical_significance":[],"seq_region_name":"7","id":"rs1796194981"},{"start":140529815,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140529815,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130476532","clinical_significance":[]},{"seq_region_name":"7","id":"rs1235422027","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140529817,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529817,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1796195140","clinical_significance":[],"start":140529823,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140529823,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140529830,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140529830,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1585559237","seq_region_name":"7"},{"id":"rs1796195409","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529832,"source":"dbSNP","strand":1,"feature_type":"variation","end":140529832,"alleles":["T","C"]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140529836,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529836,"clinical_significance":[],"seq_region_name":"7","id":"rs1277599344"},{"clinical_significance":[],"seq_region_name":"7","id":"rs995066227","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529837,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140529837},{"source":"dbSNP","start":140529838,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140529838,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1276503490"},{"seq_region_name":"7","id":"rs551563458","clinical_significance":[],"start":140529839,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A","C"],"end":140529839,"strand":1,"feature_type":"variation"},{"id":"rs945478676","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140529848,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529848,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1047525312","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529849,"feature_type":"variation","strand":1,"end":140529849,"alleles":["G","A"]},{"end":140529853,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140529853,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130476628"},{"feature_type":"variation","strand":1,"end":140529854,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529854,"clinical_significance":[],"seq_region_name":"7","id":"rs1283876712"},{"seq_region_name":"7","id":"rs1796196584","clinical_significance":[],"strand":1,"feature_type":"variation","end":140529864,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529864,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529865,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140529865,"seq_region_name":"7","id":"rs1292781556","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140529868,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529868,"clinical_significance":[],"seq_region_name":"7","id":"rs1490881617"},{"clinical_significance":[],"id":"rs982189590","seq_region_name":"7","end":140529869,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140529869,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs928178006","seq_region_name":"7","clinical_significance":[],"end":140529870,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140529870,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140529874,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140529874,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs569962641","seq_region_name":"7"},{"start":140529877,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140529877,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796197198","clinical_significance":[]},{"end":140529882,"alleles":["T","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140529882,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs938163909"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796197499","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529885,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140529885},{"feature_type":"variation","strand":1,"end":140529887,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529887,"clinical_significance":[],"seq_region_name":"7","id":"rs1008773782"},{"id":"rs188496255","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140529888,"strand":1,"feature_type":"variation","start":140529888,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140529889,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529889,"source":"dbSNP","seq_region_name":"7","id":"rs144094481","clinical_significance":[]},{"seq_region_name":"7","id":"rs1425089555","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529891,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140529891},{"seq_region_name":"7","id":"rs1410974328","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529895,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140529895},{"start":140529901,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140529901,"strand":1,"feature_type":"variation","id":"rs1186862524","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140529905,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529905,"clinical_significance":[],"id":"rs1472715375","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs930855965","feature_type":"variation","strand":1,"end":140529907,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529907},{"clinical_significance":[],"seq_region_name":"7","id":"rs1340275144","source":"dbSNP","start":140529908,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140529908,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1266007692","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529913,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140529913},{"feature_type":"variation","strand":1,"end":140529914,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529914,"clinical_significance":[],"id":"rs1469935250","seq_region_name":"7"},{"end":140529915,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140529915,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1163901156"},{"clinical_significance":[],"id":"rs1796198817","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529916,"feature_type":"variation","strand":1,"end":140529916,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796198917","source":"dbSNP","start":140529917,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140529917,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140529918,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529918,"source":"dbSNP","seq_region_name":"7","id":"rs1796199017","clinical_significance":[]},{"source":"dbSNP","start":140529926,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140529926,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1223650638"},{"feature_type":"variation","strand":1,"alleles":["AAAA","AA"],"end":140529929,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529926,"clinical_significance":[],"seq_region_name":"7","id":"rs1796199211"},{"source":"dbSNP","start":140529930,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140529930,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs996302874"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529933,"feature_type":"variation","strand":1,"end":140529933,"alleles":["A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1796199428"},{"feature_type":"variation","strand":1,"end":140529934,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529934,"clinical_significance":[],"seq_region_name":"7","id":"rs1289240011"},{"source":"dbSNP","start":140529937,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140529937,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796199605"},{"feature_type":"variation","strand":1,"end":140529945,"alleles":["ATAATAA","ATAA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529939,"clinical_significance":[],"seq_region_name":"7","id":"rs1229011750"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529940,"feature_type":"variation","strand":1,"end":140529940,"alleles":["T","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1047392432"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529941,"feature_type":"variation","strand":1,"alleles":["AATAAAA","AATAAAATAAAA"],"end":140529947,"clinical_significance":[],"seq_region_name":"7","id":"rs1796199885"},{"clinical_significance":[],"seq_region_name":"7","id":"rs886096794","feature_type":"variation","strand":1,"end":140529943,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529943},{"seq_region_name":"7","id":"rs1022372800","clinical_significance":[],"strand":1,"feature_type":"variation","end":140529960,"alleles":["AAAACAAAACAAAACAA","AAAACAAAACAA","AAAACAAAACAAAACAAAACAA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529944,"source":"dbSNP"},{"source":"dbSNP","start":140529945,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140529945,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796200398"},{"alleles":["A","G"],"end":140529949,"strand":1,"feature_type":"variation","start":140529949,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1286632513","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796200632","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529949,"source":"dbSNP","strand":1,"feature_type":"variation","end":140529952,"alleles":["AAAA","AAA"]},{"seq_region_name":"7","id":"rs568033970","clinical_significance":[],"strand":1,"feature_type":"variation","end":140529950,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529950,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529951,"source":"dbSNP","strand":1,"feature_type":"variation","end":140529951,"alleles":["A","C"],"seq_region_name":"7","id":"rs1796200923","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs774033959","feature_type":"variation","strand":1,"end":140529954,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529954},{"seq_region_name":"7","id":"rs1796201240","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529955,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140529955},{"seq_region_name":"7","id":"rs1554459925","clinical_significance":[],"start":140529956,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["-","C"],"end":140529955,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529956,"feature_type":"variation","strand":1,"end":140529956,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1796201813"},{"clinical_significance":[],"id":"rs968273977","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529956,"feature_type":"variation","strand":1,"alleles":["AACAACAACAACAACAA","AACAACAACAACAA","AACAACAACAACAACAACAA","AACAACAACAACAACAACAACAA"],"end":140529972},{"clinical_significance":[],"seq_region_name":"7","id":"rs1396549595","source":"dbSNP","start":140529959,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AA","A"],"end":140529960,"feature_type":"variation","strand":1},{"end":140529962,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140529962,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1563119801"},{"id":"rs1796202277","seq_region_name":"7","clinical_significance":[],"end":140529969,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140529969,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140529970,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140529970,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs924109917","seq_region_name":"7"},{"id":"rs1796202496","seq_region_name":"7","clinical_significance":[],"start":140529971,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140529971,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529976,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140529976,"id":"rs961252251","seq_region_name":"7","clinical_significance":[]},{"start":140529977,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140529977,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130477030","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796202682","clinical_significance":[],"alleles":["T","C"],"end":140529981,"strand":1,"feature_type":"variation","start":140529981,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529986,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140529986,"seq_region_name":"7","id":"rs1796202784","clinical_significance":[]},{"seq_region_name":"7","id":"rs1413752519","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["AAAA","AAA"],"end":140529992,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140529989,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140529992,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529992,"clinical_significance":[],"seq_region_name":"7","id":"rs1796202983"},{"alleles":["A","G"],"end":140529994,"feature_type":"variation","strand":1,"source":"dbSNP","start":140529994,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1796203064","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140529999,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140529999,"clinical_significance":[],"id":"rs1585559575","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1393114034","clinical_significance":[],"strand":1,"feature_type":"variation","end":140530005,"alleles":["G","C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530005,"source":"dbSNP"},{"start":140530006,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140530006,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs1796203410","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140530008,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140530008,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1267777928"},{"clinical_significance":[],"id":"rs1796203690","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140530009,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530009},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140530018,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530018,"source":"dbSNP","seq_region_name":"7","id":"rs1796203818","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796203954","clinical_significance":[],"start":140530021,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140530021,"strand":1,"feature_type":"variation"},{"end":140530022,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140530022,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1192920458","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530025,"feature_type":"variation","strand":1,"end":140530025,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1487467853"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1326749331","end":140530027,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140530027,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140530028,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140530028,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796204519"},{"strand":1,"feature_type":"variation","end":140530031,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530031,"source":"dbSNP","seq_region_name":"7","id":"rs768116438","clinical_significance":[]},{"clinical_significance":[],"id":"rs1796204837","seq_region_name":"7","feature_type":"variation","strand":1,"end":140530034,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530034},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530036,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","-"],"end":140530036,"seq_region_name":"7","id":"rs1286481542","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140530041,"alleles":["T","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530041,"source":"dbSNP","seq_region_name":"7","id":"rs1335014510","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530044,"feature_type":"variation","strand":1,"end":140530044,"alleles":["T","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs988298747"},{"seq_region_name":"7","id":"rs1313219550","clinical_significance":[],"alleles":["C","T"],"end":140530049,"strand":1,"feature_type":"variation","start":140530049,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530049,"feature_type":"variation","strand":1,"alleles":["CCC","CC"],"end":140530051,"clinical_significance":[],"id":"rs992360925","seq_region_name":"7"},{"alleles":["C","A","T"],"end":140530050,"feature_type":"variation","strand":1,"source":"dbSNP","start":140530050,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796205792"},{"end":140530052,"alleles":["T","-"],"strand":1,"feature_type":"variation","start":140530052,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796205913","clinical_significance":[]},{"clinical_significance":[],"id":"rs917651737","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530053,"feature_type":"variation","strand":1,"end":140530053,"alleles":["G","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796206081","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530056,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140530056},{"strand":1,"feature_type":"variation","end":140530057,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530057,"source":"dbSNP","seq_region_name":"7","id":"rs1303866733","clinical_significance":[]},{"seq_region_name":"7","id":"rs1385392888","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530058,"source":"dbSNP","strand":1,"feature_type":"variation","end":140530058,"alleles":["T","A"]},{"clinical_significance":[],"id":"rs1796206367","seq_region_name":"7","end":140530058,"alleles":["-","A","AA","AAA","AAAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140530059,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs868310885","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530059,"source":"dbSNP","strand":1,"feature_type":"variation","end":140530059,"alleles":["C","A"]},{"seq_region_name":"7","id":"rs1448493325","clinical_significance":[],"start":140530060,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140530060,"strand":1,"feature_type":"variation"},{"end":140530075,"alleles":["AAAAAAAAAAAAAAAA","AAAAAAAAAAAAA","AAAAAAAAAAAAAA","AAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140530060,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs3042405"},{"seq_region_name":"7","id":"rs1796207151","clinical_significance":[],"strand":1,"feature_type":"variation","end":140530065,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530065,"source":"dbSNP"},{"seq_region_name":"7","id":"rs760374848","clinical_significance":[],"start":140530073,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140530077,"alleles":["AAATA","AAATAAATA"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1008626956","feature_type":"variation","strand":1,"end":140530074,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530074},{"seq_region_name":"7","id":"rs916950805","clinical_significance":[],"start":140530076,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140530076,"alleles":["T","A","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1554459957","clinical_significance":[],"alleles":["A","AAAA"],"end":140530077,"strand":1,"feature_type":"variation","start":140530077,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs535446713","clinical_significance":[],"start":140530080,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","T"],"end":140530080,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs2130477398","clinical_significance":[],"end":140530083,"alleles":["TTT","TT"],"strand":1,"feature_type":"variation","start":140530081,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140530082,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140530082,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs900221907","clinical_significance":[]},{"alleles":["T","G"],"end":140530086,"feature_type":"variation","strand":1,"source":"dbSNP","start":140530086,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1244005757"},{"seq_region_name":"7","id":"rs1291185420","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530089,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140530089},{"seq_region_name":"7","id":"rs996431977","clinical_significance":[],"start":140530090,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140530090,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1563119898","clinical_significance":[],"alleles":["A","T"],"end":140530091,"strand":1,"feature_type":"variation","start":140530091,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530092,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140530092,"id":"rs1204563710","seq_region_name":"7","clinical_significance":[]},{"id":"rs1340131553","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140530100,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530100,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1796208410","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140530101,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530101},{"clinical_significance":[],"seq_region_name":"7","id":"rs1483708275","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140530107,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530107},{"clinical_significance":[],"id":"rs1198142283","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140530111,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530111},{"start":140530113,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140530113,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1257925646","clinical_significance":[]},{"alleles":["G","A"],"end":140530122,"strand":1,"feature_type":"variation","start":140530122,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585559842","clinical_significance":[]},{"seq_region_name":"7","id":"rs1044151942","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530128,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140530128},{"id":"rs920352283","seq_region_name":"7","clinical_significance":[],"end":140530130,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140530130,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140530136,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530136,"source":"dbSNP","seq_region_name":"7","id":"rs1796209101","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530141,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140530141,"clinical_significance":[],"id":"rs1299062069","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1249029019","seq_region_name":"7","feature_type":"variation","strand":1,"end":140530142,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530142},{"end":140530143,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140530143,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs930386920","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1366827382","feature_type":"variation","strand":1,"alleles":["T","A"],"end":140530148,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530148},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796209588","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530152,"feature_type":"variation","strand":1,"end":140530152,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs10156199","feature_type":"variation","strand":1,"end":140530153,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530153},{"source":"dbSNP","start":140530167,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140530167,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796209800"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796209890","source":"dbSNP","start":140530168,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140530168,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1585559912","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530171,"feature_type":"variation","strand":1,"end":140530171,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1381107501","clinical_significance":[],"strand":1,"feature_type":"variation","end":140530172,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530172,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1402498849","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530173,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140530173},{"id":"rs886238157","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530178,"source":"dbSNP","strand":1,"feature_type":"variation","end":140530178,"alleles":["C","A","T"]},{"seq_region_name":"7","id":"rs144406779","clinical_significance":[],"strand":1,"feature_type":"variation","end":140530179,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530179,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1796210408","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530187,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140530187},{"source":"dbSNP","start":140530188,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140530188,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs988719502"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140530190,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530190,"clinical_significance":[],"seq_region_name":"7","id":"rs539788455"},{"start":140530192,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140530192,"strand":1,"feature_type":"variation","id":"rs1585559971","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140530194,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C","G"],"end":140530194,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs759224886"},{"feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140530197,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530197,"clinical_significance":[],"seq_region_name":"7","id":"rs558072202"},{"clinical_significance":[],"seq_region_name":"7","id":"rs928050679","source":"dbSNP","start":140530198,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140530198,"alleles":["T","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1443030642","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140530200,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530200},{"seq_region_name":"7","id":"rs1796211203","clinical_significance":[],"start":140530203,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140530203,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"end":140530207,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140530207,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796211297"},{"source":"dbSNP","start":140530209,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140530209,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1373202428"},{"alleles":["G","C"],"end":140530210,"feature_type":"variation","strand":1,"source":"dbSNP","start":140530210,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796211488"},{"seq_region_name":"7","id":"rs959460096","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530211,"source":"dbSNP","strand":1,"feature_type":"variation","end":140530211,"alleles":["G","A"]},{"source":"dbSNP","start":140530213,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140530213,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1796211642","seq_region_name":"7"},{"id":"rs1796211731","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530214,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140530214},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530215,"source":"dbSNP","strand":1,"feature_type":"variation","end":140530215,"alleles":["C","A"],"id":"rs1258577540","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs991397246","clinical_significance":[],"start":140530216,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140530216,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"end":140530234,"alleles":["CAACAACAACAA","CAACAACAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140530223,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs996165870","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530226,"source":"dbSNP","strand":1,"feature_type":"variation","end":140530226,"alleles":["C","A","T"],"seq_region_name":"7","id":"rs117576689","clinical_significance":[]},{"end":140530228,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140530228,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1796212259","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530234,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140530234,"seq_region_name":"7","id":"rs543233142","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140530236,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530236,"source":"dbSNP","seq_region_name":"7","id":"rs1796212450","clinical_significance":[]},{"end":140530243,"alleles":["ATCATCAT","ATCAT"],"strand":1,"feature_type":"variation","start":140530236,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1340681903","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs80164834","source":"dbSNP","start":140530238,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140530238,"alleles":["C","A"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140530245,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140530245,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs2130477854","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140530251,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530251,"clinical_significance":[],"seq_region_name":"7","id":"rs1796212701"},{"clinical_significance":[],"id":"rs999579579","seq_region_name":"7","source":"dbSNP","start":140530252,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140530252,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs147977731","end":140530253,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140530253,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796212982","end":140530255,"alleles":["-","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140530256,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530256,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140530256,"id":"rs1796213109","seq_region_name":"7","clinical_significance":[]},{"start":140530257,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140530257,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs907578061","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1031596871","feature_type":"variation","strand":1,"end":140530259,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530259},{"seq_region_name":"7","id":"rs1796213393","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530262,"source":"dbSNP","strand":1,"feature_type":"variation","end":140530262,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796213490","end":140530267,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140530267,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140530269,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530269,"source":"dbSNP","seq_region_name":"7","id":"rs944390948","clinical_significance":[]},{"seq_region_name":"7","id":"rs960901034","clinical_significance":[],"end":140530273,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140530273,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1585560127","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530274,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140530274},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140530275,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530275,"clinical_significance":[],"seq_region_name":"7","id":"rs1393924886"},{"seq_region_name":"7","id":"rs1395705365","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530278,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140530278},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796214116","source":"dbSNP","start":140530282,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140530282,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530286,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140530286,"clinical_significance":[],"id":"rs1040017984","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140530288,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530288,"clinical_significance":[],"seq_region_name":"7","id":"rs1374398630"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796214403","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530289,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140530289},{"clinical_significance":[],"id":"rs1796214513","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140530296,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530296},{"id":"rs1796214619","seq_region_name":"7","clinical_significance":[],"start":140530300,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140530300,"alleles":["T","A","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs916815361","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140530301,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530301,"source":"dbSNP"},{"end":140530306,"alleles":["AAAAAA","AAAAAAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140530301,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1470213706"},{"alleles":["A","T"],"end":140530304,"strand":1,"feature_type":"variation","start":140530304,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1563120051","seq_region_name":"7","clinical_significance":[]},{"end":140530307,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140530307,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796214948","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140530309,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530309,"clinical_significance":[],"seq_region_name":"7","id":"rs1380270126"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140530313,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530313,"clinical_significance":[],"seq_region_name":"7","id":"rs1450791490"},{"source":"dbSNP","start":140530318,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140530318,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs774931575","seq_region_name":"7"},{"start":140530325,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140530325,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1312264060","clinical_significance":[]},{"seq_region_name":"7","id":"rs1327170803","clinical_significance":[],"end":140530344,"alleles":["TTTTCCATTCCCCAATTT","TTT"],"strand":1,"feature_type":"variation","start":140530327,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530333,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140530333,"clinical_significance":[],"seq_region_name":"7","id":"rs868557832"},{"seq_region_name":"7","id":"rs1370258832","clinical_significance":[],"end":140530338,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140530338,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1054731659","seq_region_name":"7","source":"dbSNP","start":140530340,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140530340,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140530341,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140530341,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs116063057"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530343,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140530343,"clinical_significance":[],"seq_region_name":"7","id":"rs1796215929"},{"seq_region_name":"7","id":"rs1796216013","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140530350,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530350,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140530352,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530352,"clinical_significance":[],"seq_region_name":"7","id":"rs1475008572"},{"source":"dbSNP","start":140530354,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","-"],"end":140530354,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1252744620","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1184817511","clinical_significance":[],"start":140530357,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140530357,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140530363,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140530363,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130478143"},{"end":140530366,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140530366,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1339340941"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796216516","feature_type":"variation","strand":1,"end":140530368,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530368},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530370,"source":"dbSNP","strand":1,"feature_type":"variation","end":140530370,"alleles":["C","T"],"seq_region_name":"7","id":"rs1796216597","clinical_significance":[]},{"source":"dbSNP","start":140530371,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140530371,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1796216689","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1796216777","clinical_significance":[],"alleles":["T","C"],"end":140530373,"strand":1,"feature_type":"variation","start":140530373,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140530374,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140530375,"alleles":["TG","-"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796216870","clinical_significance":[]},{"end":140530379,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140530379,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1272976289","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs979756259","alleles":["G","A","C"],"end":140530382,"feature_type":"variation","strand":1,"source":"dbSNP","start":140530382,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796217168","feature_type":"variation","strand":1,"end":140530384,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530384},{"seq_region_name":"7","id":"rs1201409107","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530389,"source":"dbSNP","strand":1,"feature_type":"variation","end":140530389,"alleles":["T","A"]},{"alleles":["C","A"],"end":140530393,"feature_type":"variation","strand":1,"source":"dbSNP","start":140530393,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs2130478243","seq_region_name":"7"},{"end":140530395,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140530395,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs2130478254","seq_region_name":"7"},{"source":"dbSNP","start":140530404,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140530404,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1356516674"},{"seq_region_name":"7","id":"rs1266701281","clinical_significance":[],"start":140530408,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140530408,"alleles":["C","A","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs747744699","clinical_significance":[],"strand":1,"feature_type":"variation","end":140530411,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530411,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1354451453","seq_region_name":"7","alleles":["T","A"],"end":140530415,"feature_type":"variation","strand":1,"source":"dbSNP","start":140530415,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1288540874","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530417,"feature_type":"variation","strand":1,"end":140530417,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130478307","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530418,"feature_type":"variation","strand":1,"end":140530418,"alleles":["T","C"]},{"end":140530421,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140530421,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1796217947","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530423,"source":"dbSNP","strand":1,"feature_type":"variation","end":140530423,"alleles":["C","T"],"seq_region_name":"7","id":"rs1411467579","clinical_significance":[]},{"clinical_significance":[],"id":"rs73163301","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530434,"feature_type":"variation","strand":1,"end":140530434,"alleles":["A","G","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1328162841","source":"dbSNP","start":140530436,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140530436,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs569579904","feature_type":"variation","strand":1,"end":140530437,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530437},{"seq_region_name":"7","id":"rs971273744","clinical_significance":[],"strand":1,"feature_type":"variation","end":140530442,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530442,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1161553399","clinical_significance":[],"start":140530449,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G","T"],"end":140530449,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1796218781","clinical_significance":[],"start":140530453,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140530453,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1460247444","source":"dbSNP","start":140530455,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140530455,"alleles":["G","A"],"feature_type":"variation","strand":1},{"end":140530458,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140530458,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1796218868","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140530467,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140530467,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1413017457","seq_region_name":"7"},{"id":"rs1182666154","seq_region_name":"7","clinical_significance":[],"end":140530474,"alleles":["AGCAGCA","AGCA"],"strand":1,"feature_type":"variation","start":140530468,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530469,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140530469,"clinical_significance":[],"seq_region_name":"7","id":"rs10280493"},{"id":"rs1796219370","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140530470,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530470,"source":"dbSNP"},{"id":"rs1796219467","seq_region_name":"7","clinical_significance":[],"start":140530471,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140530471,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140530474,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530474,"source":"dbSNP","seq_region_name":"7","id":"rs1796219572","clinical_significance":[]},{"seq_region_name":"7","id":"rs1471844318","clinical_significance":[],"end":140530475,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140530475,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["A","C"],"end":140530479,"feature_type":"variation","strand":1,"source":"dbSNP","start":140530479,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796219766"},{"strand":1,"feature_type":"variation","end":140530484,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530484,"source":"dbSNP","seq_region_name":"7","id":"rs552316252","clinical_significance":[]},{"end":140530485,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140530485,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs115357163"},{"clinical_significance":[],"seq_region_name":"7","id":"rs762221496","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140530487,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530487},{"start":140530489,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140530489,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1190432246","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140530490,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530490,"source":"dbSNP","id":"rs1265825113","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140530492,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530492,"clinical_significance":[],"seq_region_name":"7","id":"rs1796220289"},{"seq_region_name":"7","id":"rs1211313233","clinical_significance":[],"start":140530493,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140530493,"strand":1,"feature_type":"variation"},{"start":140530497,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140530497,"alleles":["T","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796220489","clinical_significance":[]},{"clinical_significance":[],"id":"rs959727123","seq_region_name":"7","source":"dbSNP","start":140530499,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140530499,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530501,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140530501,"clinical_significance":[],"seq_region_name":"7","id":"rs376705212"},{"strand":1,"feature_type":"variation","end":140530502,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530502,"source":"dbSNP","seq_region_name":"7","id":"rs990910376","clinical_significance":[]},{"source":"dbSNP","start":140530503,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140530503,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1268420334"},{"clinical_significance":[],"id":"rs1229835315","seq_region_name":"7","source":"dbSNP","start":140530504,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140530504,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1348364090","feature_type":"variation","strand":1,"end":140530505,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530505},{"seq_region_name":"7","id":"rs1796221251","clinical_significance":[],"strand":1,"feature_type":"variation","end":140530507,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530507,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796221355","feature_type":"variation","strand":1,"alleles":["C","-"],"end":140530516,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530516},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796221453","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530520,"feature_type":"variation","strand":1,"end":140530520,"alleles":["C","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1278746744","alleles":["A","G"],"end":140530523,"feature_type":"variation","strand":1,"source":"dbSNP","start":140530523,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs920797647","clinical_significance":[],"alleles":["C","T"],"end":140530528,"strand":1,"feature_type":"variation","start":140530528,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1332786936","source":"dbSNP","start":140530531,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140530531,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796221846","source":"dbSNP","start":140530532,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140530532,"alleles":["C","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1796221923","seq_region_name":"7","source":"dbSNP","start":140530533,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140530533,"alleles":["C","T"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140530540,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140530540,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796222025"},{"seq_region_name":"7","id":"rs1796222117","clinical_significance":[],"start":140530548,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","T"],"end":140530548,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs78284578","source":"dbSNP","start":140530549,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140530549,"feature_type":"variation","strand":1},{"start":140530552,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140530552,"alleles":["A","G"],"strand":1,"feature_type":"variation","id":"rs114845959","seq_region_name":"7","clinical_significance":[]},{"id":"rs1796222484","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140530553,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530553,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530554,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140530554,"seq_region_name":"7","id":"rs1440313474","clinical_significance":[]},{"seq_region_name":"7","id":"rs1161725554","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140530555,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530555,"source":"dbSNP"},{"end":140530557,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140530557,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796222811"},{"id":"rs1455846766","seq_region_name":"7","clinical_significance":[],"alleles":["A","G"],"end":140530565,"strand":1,"feature_type":"variation","start":140530565,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1407452921","clinical_significance":[],"strand":1,"feature_type":"variation","end":140530569,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530569,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1585560642","clinical_significance":[],"start":140530576,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140530576,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140530580,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530580,"clinical_significance":[],"id":"rs1796223226","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["C","-"],"end":140530580,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530580,"clinical_significance":[],"seq_region_name":"7","id":"rs1796223321"},{"seq_region_name":"7","id":"rs1796223415","clinical_significance":[],"start":140530584,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140530584,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1796223518","seq_region_name":"7","end":140530586,"alleles":["TT","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140530585,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1796223616","clinical_significance":[],"start":140530585,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TTCTTT","TT"],"end":140530590,"strand":1,"feature_type":"variation"},{"alleles":["T","G"],"end":140530588,"strand":1,"feature_type":"variation","start":140530588,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs931864875","clinical_significance":[]},{"seq_region_name":"7","id":"rs1563120216","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140530590,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530590,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs531030909","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140530592,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530592},{"start":140530596,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140530596,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796224039","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs908154956","source":"dbSNP","start":140530597,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140530597,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796224236","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530598,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140530598},{"source":"dbSNP","start":140530599,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140530599,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796224324"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585560686","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530600,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140530600},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140530606,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530606,"source":"dbSNP","seq_region_name":"7","id":"rs1796224517","clinical_significance":[]},{"source":"dbSNP","start":140530610,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140530610,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130478861"},{"seq_region_name":"7","id":"rs1796224627","clinical_significance":[],"end":140530613,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140530613,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1796224707","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140530614,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530614,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1193531211","end":140530615,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140530615,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796224892","source":"dbSNP","start":140530618,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140530618,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530621,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140530621,"seq_region_name":"7","id":"rs1467684141","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796225094","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140530623,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530623,"source":"dbSNP"},{"source":"dbSNP","start":140530627,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140530627,"alleles":["A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796225184"},{"alleles":["T","A"],"end":140530628,"strand":1,"feature_type":"variation","start":140530628,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1469098414","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1385976810","source":"dbSNP","start":140530630,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140530630,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140530630,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["CC","C"],"end":140530631,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs759086668"},{"source":"dbSNP","start":140530631,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140530631,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1384095814"},{"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140530632,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530632,"source":"dbSNP","id":"rs1796226020","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1219623175","clinical_significance":[],"strand":1,"feature_type":"variation","end":140530634,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530634,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs534845648","alleles":["AAAAAAAAAA","AAAAAAAA","AAAAAAAAA","AAAAAAAAAAA"],"end":140530644,"feature_type":"variation","strand":1,"source":"dbSNP","start":140530635,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140530636,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140530636,"strand":1,"feature_type":"variation","id":"rs1563120240","seq_region_name":"7","clinical_significance":[]},{"end":140530642,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140530642,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1000056817"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796226920","source":"dbSNP","start":140530643,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140530643,"alleles":["A","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs201074981","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530644,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140530644},{"end":140530647,"alleles":["AGAG","AG"],"strand":1,"feature_type":"variation","start":140530644,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1233459981","clinical_significance":[]},{"seq_region_name":"7","id":"rs868280353","clinical_significance":[],"end":140530645,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140530645,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140530647,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530647,"source":"dbSNP","seq_region_name":"7","id":"rs896674283","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530648,"feature_type":"variation","strand":1,"end":140530648,"alleles":["T","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585560843"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530651,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140530651,"seq_region_name":"7","id":"rs1796227717","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140530669,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530669,"clinical_significance":[],"id":"rs2130479070","seq_region_name":"7"},{"start":140530674,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140530674,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs370110909","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140530675,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530675,"clinical_significance":[],"id":"rs1796228006","seq_region_name":"7"},{"source":"dbSNP","start":140530680,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140530680,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1428661197"},{"strand":1,"feature_type":"variation","end":140530685,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530685,"source":"dbSNP","id":"rs141611588","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530686,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140530686,"clinical_significance":[],"seq_region_name":"7","id":"rs1796228430"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796228568","alleles":["A","G"],"end":140530687,"feature_type":"variation","strand":1,"source":"dbSNP","start":140530687,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs944921119","feature_type":"variation","strand":1,"end":140530688,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530688},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140530690,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530690,"source":"dbSNP","id":"rs1796228837","seq_region_name":"7","clinical_significance":[]},{"start":140530691,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140530691,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796228989","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs553460960","source":"dbSNP","start":140530692,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140530692,"alleles":["C","G"],"feature_type":"variation","strand":1},{"end":140530695,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140530695,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796229299"},{"seq_region_name":"7","id":"rs969614417","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530700,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140530700},{"start":140530702,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140530702,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1393639139","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530703,"feature_type":"variation","strand":1,"end":140530703,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1796229773"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796229911","source":"dbSNP","start":140530708,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140530708,"alleles":["G","C"],"feature_type":"variation","strand":1},{"end":140530710,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140530710,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796230051","clinical_significance":[]},{"start":140530714,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140530714,"alleles":["G","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs974261996","clinical_significance":[]},{"alleles":["T","C"],"end":140530716,"feature_type":"variation","strand":1,"source":"dbSNP","start":140530716,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1450646711"},{"clinical_significance":[],"id":"rs1796230506","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140530722,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530722},{"seq_region_name":"7","id":"rs1392511317","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530727,"source":"dbSNP","strand":1,"feature_type":"variation","end":140530727,"alleles":["C","A"]},{"clinical_significance":[],"id":"rs1027766958","seq_region_name":"7","source":"dbSNP","start":140530732,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140530732,"alleles":["T","C"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140530732,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TCTTTCTTT","TCTTT"],"end":140530740,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1189970547"},{"clinical_significance":[],"seq_region_name":"7","id":"rs951743946","end":140530737,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140530737,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140530748,"alleles":["TTTTTTTTTTT","TTTTTTTTTT","TTTTTTTTTTTT","TTTTTTTTTTTTT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530738,"clinical_significance":[],"seq_region_name":"7","id":"rs199738093"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530739,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140530739,"seq_region_name":"7","id":"rs1209810558","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140530747,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530747,"source":"dbSNP","seq_region_name":"7","id":"rs1203443798","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1299679249","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530749,"feature_type":"variation","strand":1,"end":140530749,"alleles":["G","T"]},{"id":"rs1212924082","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140530753,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530753,"source":"dbSNP"},{"end":140530772,"alleles":["ATTTCACTCTGTCTCC","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140530757,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796232137"},{"feature_type":"variation","strand":1,"end":140530760,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530760,"clinical_significance":[],"id":"rs1361328172","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs568670898","source":"dbSNP","start":140530763,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140530766,"alleles":["CTCT","CT"],"feature_type":"variation","strand":1},{"alleles":["T","C"],"end":140530764,"feature_type":"variation","strand":1,"source":"dbSNP","start":140530764,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796232659"},{"seq_region_name":"7","id":"rs1450456924","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530769,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140530769},{"seq_region_name":"7","id":"rs1373787959","clinical_significance":[],"start":140530770,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140530770,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs921607474","source":"dbSNP","start":140530775,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140530775,"alleles":["G","A"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140530782,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530782,"clinical_significance":[],"seq_region_name":"7","id":"rs907604244"},{"seq_region_name":"7","id":"rs944409439","clinical_significance":[],"end":140530785,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140530785,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs776666265","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530792,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140530792},{"seq_region_name":"7","id":"rs1168918257","clinical_significance":[],"alleles":["T","G"],"end":140530796,"strand":1,"feature_type":"variation","start":140530796,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1407761724","source":"dbSNP","start":140530800,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140530800,"alleles":["A","C","G"],"feature_type":"variation","strand":1},{"id":"rs1054193326","seq_region_name":"7","clinical_significance":[],"end":140530807,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140530807,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140530808,"alleles":["G","C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530808,"clinical_significance":[],"id":"rs1585561180","seq_region_name":"7"},{"alleles":["C","A"],"end":140530809,"feature_type":"variation","strand":1,"source":"dbSNP","start":140530809,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1473578577"},{"seq_region_name":"7","id":"rs1585561195","clinical_significance":[],"alleles":["A","C"],"end":140530811,"strand":1,"feature_type":"variation","start":140530811,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530812,"feature_type":"variation","strand":1,"end":140530812,"alleles":["C","A"],"clinical_significance":[],"id":"rs1796234658","seq_region_name":"7"},{"seq_region_name":"7","id":"rs2130479457","clinical_significance":[],"strand":1,"feature_type":"variation","end":140530813,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530813,"source":"dbSNP"},{"seq_region_name":"7","id":"rs893003461","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530815,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140530815},{"seq_region_name":"7","id":"rs528933484","clinical_significance":[],"start":140530816,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140530816,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1585561225","clinical_significance":[],"end":140530817,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140530817,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs150515639","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140530818,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530818,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1159602434","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530823,"source":"dbSNP","strand":1,"feature_type":"variation","end":140530823,"alleles":["C","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530824,"source":"dbSNP","strand":1,"feature_type":"variation","end":140530824,"alleles":["G","A"],"seq_region_name":"7","id":"rs907120741","clinical_significance":[]},{"seq_region_name":"7","id":"rs1365293059","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530826,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140530826},{"feature_type":"variation","strand":1,"end":140530833,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530833,"clinical_significance":[],"id":"rs1796235892","seq_region_name":"7"},{"seq_region_name":"7","id":"rs903875182","clinical_significance":[],"start":140530834,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140530834,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140530836,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140530836,"alleles":["T","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1002758044"},{"seq_region_name":"7","id":"rs1035463077","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530838,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140530838},{"alleles":["C","T"],"end":140530840,"feature_type":"variation","strand":1,"source":"dbSNP","start":140530840,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs935332169","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140530842,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530842,"source":"dbSNP","id":"rs1796236389","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1353827409","source":"dbSNP","start":140530844,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140530844,"alleles":["C","T"],"feature_type":"variation","strand":1},{"start":140530848,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140530848,"strand":1,"feature_type":"variation","id":"rs1796236581","seq_region_name":"7","clinical_significance":[]},{"start":140530849,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140530849,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796236669","clinical_significance":[]},{"source":"dbSNP","start":140530850,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140530850,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796236771"},{"seq_region_name":"7","id":"rs1455583213","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C","T"],"end":140530855,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530855,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530857,"source":"dbSNP","strand":1,"feature_type":"variation","end":140530857,"alleles":["T","C"],"id":"rs1292864100","seq_region_name":"7","clinical_significance":[]},{"end":140530858,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140530858,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796237081"},{"start":140530858,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["GTAGCTGAG","GTAGCTGAGTAGCTGAG"],"end":140530866,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796237191","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530860,"source":"dbSNP","strand":1,"feature_type":"variation","end":140530860,"alleles":["A","G"],"seq_region_name":"7","id":"rs1796237305","clinical_significance":[]},{"clinical_significance":[],"id":"rs1410876051","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530863,"feature_type":"variation","strand":1,"end":140530863,"alleles":["T","C"]},{"start":140530866,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140530866,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796237488","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796237582","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530867,"feature_type":"variation","strand":1,"alleles":["ATTAACAGGCA","-"],"end":140530877},{"seq_region_name":"7","id":"rs139491302","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530880,"source":"dbSNP","strand":1,"feature_type":"variation","end":140530880,"alleles":["C","A","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1461917780","source":"dbSNP","start":140530881,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140530881,"feature_type":"variation","strand":1},{"id":"rs1012766361","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530883,"source":"dbSNP","strand":1,"feature_type":"variation","end":140530883,"alleles":["C","T"]},{"source":"dbSNP","start":140530885,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140530885,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796238689"},{"seq_region_name":"7","id":"rs1796238790","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530886,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140530886},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796238881","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530892,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140530892},{"strand":1,"feature_type":"variation","end":140530893,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530893,"source":"dbSNP","seq_region_name":"7","id":"rs1796238969","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796239071","clinical_significance":[],"start":140530911,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140530911,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530912,"source":"dbSNP","strand":1,"feature_type":"variation","end":140530912,"alleles":["G","T"],"seq_region_name":"7","id":"rs1027755199","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796239278","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530915,"feature_type":"variation","strand":1,"end":140530915,"alleles":["A","G"]},{"source":"dbSNP","start":140530919,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140530919,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796239389"},{"clinical_significance":[],"seq_region_name":"7","id":"rs539427121","source":"dbSNP","start":140530921,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140530921,"feature_type":"variation","strand":1},{"alleles":["G","A"],"end":140530922,"strand":1,"feature_type":"variation","start":140530922,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs952108810","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1462521430","source":"dbSNP","start":140530929,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C","G"],"end":140530929,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140530930,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530930,"clinical_significance":[],"id":"rs1013584271","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1796239915","seq_region_name":"7","alleles":["C","A"],"end":140530931,"feature_type":"variation","strand":1,"source":"dbSNP","start":140530931,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs983588158","end":140530933,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140530933,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530934,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140530934,"id":"rs751627016","seq_region_name":"7","clinical_significance":[]},{"id":"rs1023766556","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140530936,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530936,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530937,"source":"dbSNP","strand":1,"feature_type":"variation","end":140530937,"alleles":["G","T"],"id":"rs558115126","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530938,"source":"dbSNP","strand":1,"feature_type":"variation","end":140530938,"alleles":["G","A","C"],"seq_region_name":"7","id":"rs1015014147","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140530944,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530944,"clinical_significance":[],"id":"rs181522651","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1796241076","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140530947,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530947,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796241230","end":140530950,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140530950,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140530951,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530951,"clinical_significance":[],"seq_region_name":"7","id":"rs1219119596"},{"source":"dbSNP","start":140530952,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140530952,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1247166426"},{"id":"rs370128871","seq_region_name":"7","clinical_significance":[],"start":140530955,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","T"],"end":140530955,"strand":1,"feature_type":"variation"},{"alleles":["T","-"],"end":140530956,"feature_type":"variation","strand":1,"source":"dbSNP","start":140530956,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1332730948","seq_region_name":"7"},{"source":"dbSNP","start":140530959,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140530959,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796242056"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530961,"source":"dbSNP","strand":1,"feature_type":"variation","end":140530961,"alleles":["A","G"],"seq_region_name":"7","id":"rs1796242205","clinical_significance":[]},{"clinical_significance":[],"id":"rs1796242361","seq_region_name":"7","source":"dbSNP","start":140530962,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140530962,"alleles":["C","A","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs966301741","seq_region_name":"7","alleles":["C","T"],"end":140530965,"feature_type":"variation","strand":1,"source":"dbSNP","start":140530965,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs905361452","clinical_significance":[],"end":140530966,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140530966,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796242836","end":140530967,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140530967,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs976359993","seq_region_name":"7","feature_type":"variation","strand":1,"end":140530968,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530968},{"end":140530970,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140530970,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1796243094","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","T"],"end":140530971,"feature_type":"variation","strand":1,"source":"dbSNP","start":140530971,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585561518"},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140530973,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530973,"clinical_significance":[],"seq_region_name":"7","id":"rs921617800"},{"seq_region_name":"7","id":"rs1796243327","clinical_significance":[],"strand":1,"feature_type":"variation","end":140530974,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140530974,"source":"dbSNP"},{"id":"rs1305317034","seq_region_name":"7","clinical_significance":[],"end":140530980,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140530980,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1391125315","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140530982,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530982},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796243644","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140530987,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530987},{"alleles":["C","T"],"end":140530991,"strand":1,"feature_type":"variation","start":140530991,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1236506664","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1796243844","seq_region_name":"7","source":"dbSNP","start":140530995,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140530995,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1368951706","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530998,"feature_type":"variation","strand":1,"end":140530998,"alleles":["C","G","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1295769438","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140530999,"feature_type":"variation","strand":1,"end":140530999,"alleles":["T","C"]},{"id":"rs1796244157","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140531001,"strand":1,"feature_type":"variation","start":140531001,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140531010,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140531010,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796244240","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140531011,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531011,"clinical_significance":[],"seq_region_name":"7","id":"rs1442527262"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140531012,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531012,"source":"dbSNP","seq_region_name":"7","id":"rs755081032","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140531013,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531013,"clinical_significance":[],"seq_region_name":"7","id":"rs2130480110"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531014,"feature_type":"variation","strand":1,"end":140531014,"alleles":["G","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1324877020"},{"clinical_significance":[],"seq_region_name":"7","id":"rs996199568","feature_type":"variation","strand":1,"end":140531017,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531017},{"clinical_significance":[],"seq_region_name":"7","id":"rs990193529","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531021,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140531021},{"seq_region_name":"7","id":"rs2130480136","clinical_significance":[],"start":140531022,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140531022,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs537268554","alleles":["C","T"],"end":140531023,"feature_type":"variation","strand":1,"source":"dbSNP","start":140531023,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140531024,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140531024,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1796244931","seq_region_name":"7"},{"start":140531025,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A","C"],"end":140531025,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1027221122","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs114118543","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531027,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140531027},{"clinical_significance":[],"seq_region_name":"7","id":"rs945738571","end":140531028,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140531028,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531031,"feature_type":"variation","strand":1,"end":140531031,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1177688805"},{"id":"rs1252473228","seq_region_name":"7","clinical_significance":[],"end":140531032,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140531032,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140531034,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140531034,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1796245536","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140531038,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531038,"source":"dbSNP","seq_region_name":"7","id":"rs143311820","clinical_significance":[]},{"source":"dbSNP","start":140531039,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140531039,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs2130480236","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796245717","end":140531040,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140531040,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1209366543","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531041,"source":"dbSNP","strand":1,"feature_type":"variation","end":140531041,"alleles":["G","C"]},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140531042,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531042,"clinical_significance":[],"seq_region_name":"7","id":"rs1796245909"},{"strand":1,"feature_type":"variation","end":140531047,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531047,"source":"dbSNP","id":"rs907025881","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140531048,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531048,"clinical_significance":[],"id":"rs146241947","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1238830423","clinical_significance":[],"strand":1,"feature_type":"variation","end":140531051,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531051,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1379928171","end":140531052,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140531052,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs965790259","feature_type":"variation","strand":1,"end":140531053,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531053},{"source":"dbSNP","start":140531054,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140531054,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1796246481","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1304126889","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531055,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140531055},{"start":140531061,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140531061,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585561777","clinical_significance":[]},{"seq_region_name":"7","id":"rs1181602895","clinical_significance":[],"alleles":["A","G"],"end":140531063,"strand":1,"feature_type":"variation","start":140531063,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140531066,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140531066,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1796246815","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531066,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TCTTCT","TCT"],"end":140531071,"id":"rs373850391","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1055695624","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140531067,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531067,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140531070,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531070,"clinical_significance":[],"seq_region_name":"7","id":"rs1796247125"},{"alleles":["T","A"],"end":140531071,"feature_type":"variation","strand":1,"source":"dbSNP","start":140531071,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796247206"},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140531079,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531079,"source":"dbSNP","seq_region_name":"7","id":"rs1302077072","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140531082,"alleles":["A","AA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531082,"source":"dbSNP","id":"rs1363760497","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","A","C"],"end":140531085,"feature_type":"variation","strand":1,"source":"dbSNP","start":140531085,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs975797569"},{"feature_type":"variation","strand":1,"end":140531086,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531086,"clinical_significance":[],"seq_region_name":"7","id":"rs894357109"},{"end":140531087,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140531087,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796247742","clinical_significance":[]},{"id":"rs1796247818","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531088,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140531088},{"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140531092,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531092,"source":"dbSNP","id":"rs1412946431","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140531094,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140531094,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1299233264"},{"clinical_significance":[],"seq_region_name":"7","id":"rs114742503","feature_type":"variation","strand":1,"end":140531098,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531098},{"feature_type":"variation","strand":1,"end":140531100,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531100,"clinical_significance":[],"seq_region_name":"7","id":"rs1175514504"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796248318","source":"dbSNP","start":140531104,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140531104,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1585561885","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531106,"source":"dbSNP","strand":1,"feature_type":"variation","end":140531106,"alleles":["T","C"]},{"start":140531119,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140531119,"alleles":["T","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585561896","clinical_significance":[]},{"end":140531124,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140531124,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796248594","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796248690","source":"dbSNP","start":140531135,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140531135,"alleles":["C","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs76669966","alleles":["G","A"],"end":140531140,"feature_type":"variation","strand":1,"source":"dbSNP","start":140531140,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1308911907","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531142,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140531142},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796248987","end":140531153,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140531153,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531157,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140531157,"clinical_significance":[],"seq_region_name":"7","id":"rs749234045"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796249253","alleles":["A","G"],"end":140531158,"feature_type":"variation","strand":1,"source":"dbSNP","start":140531158,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140531160,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140531160,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs887872050","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1004916336","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140531166,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531166},{"clinical_significance":[],"seq_region_name":"7","id":"rs1359740180","source":"dbSNP","start":140531167,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140531167,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs139333859","alleles":["C","T"],"end":140531169,"feature_type":"variation","strand":1,"source":"dbSNP","start":140531169,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531173,"source":"dbSNP","strand":1,"feature_type":"variation","end":140531173,"alleles":["G","-"],"seq_region_name":"7","id":"rs1796250040","clinical_significance":[]},{"source":"dbSNP","start":140531178,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140531178,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs966220248","seq_region_name":"7"},{"id":"rs1796250339","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531180,"source":"dbSNP","strand":1,"feature_type":"variation","end":140531182,"alleles":["AAA","AA"]},{"clinical_significance":[],"id":"rs1796250504","seq_region_name":"7","end":140531184,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140531184,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs375148649","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","-"],"end":140531185,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531185,"source":"dbSNP"},{"start":140531187,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140531187,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585561966","clinical_significance":[]},{"clinical_significance":[],"id":"rs2130480644","seq_region_name":"7","end":140531188,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140531188,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140531191,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531191,"source":"dbSNP","seq_region_name":"7","id":"rs935219022","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531192,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140531192,"seq_region_name":"7","id":"rs2130480672","clinical_significance":[]},{"start":140531204,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140531204,"strand":1,"feature_type":"variation","id":"rs1796251179","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","G"],"end":140531206,"feature_type":"variation","strand":1,"source":"dbSNP","start":140531206,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2363830"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1282916756","end":140531209,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140531209,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796251749","source":"dbSNP","start":140531210,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140531210,"feature_type":"variation","strand":1},{"id":"rs1320576097","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140531211,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531211,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1209099593","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531212,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140531212},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796252154","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531214,"feature_type":"variation","strand":1,"end":140531214,"alleles":["A","T"]},{"strand":1,"feature_type":"variation","end":140531229,"alleles":["TTTTTTT","TTTTTTTT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531223,"source":"dbSNP","seq_region_name":"7","id":"rs1347815318","clinical_significance":[]},{"end":140531229,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140531229,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796252342"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140531231,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531231,"clinical_significance":[],"seq_region_name":"7","id":"rs144140137"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531232,"source":"dbSNP","strand":1,"feature_type":"variation","end":140531232,"alleles":["T","A"],"seq_region_name":"7","id":"rs1228553185","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531233,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140531233,"id":"rs1327657668","seq_region_name":"7","clinical_significance":[]},{"end":140531242,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140531242,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796252829"},{"alleles":["C","T"],"end":140531244,"strand":1,"feature_type":"variation","start":140531244,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1293070848","clinical_significance":[]},{"seq_region_name":"7","id":"rs1381303562","clinical_significance":[],"end":140531245,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140531245,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs953733748","seq_region_name":"7","source":"dbSNP","start":140531248,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140531248,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140531250,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531250,"source":"dbSNP","seq_region_name":"7","id":"rs1379364955","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140531253,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531253,"source":"dbSNP","seq_region_name":"7","id":"rs949504523","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531255,"source":"dbSNP","strand":1,"feature_type":"variation","end":140531255,"alleles":["C","A","G","T"],"seq_region_name":"7","id":"rs1253007510","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1479583201","feature_type":"variation","strand":1,"end":140531256,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531256},{"clinical_significance":[],"id":"rs1796253790","seq_region_name":"7","alleles":["G","T"],"end":140531258,"feature_type":"variation","strand":1,"source":"dbSNP","start":140531258,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1796253880","clinical_significance":[],"strand":1,"feature_type":"variation","end":140531259,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531259,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140531261,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531261,"source":"dbSNP","seq_region_name":"7","id":"rs1045123901","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1371398469","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531262,"feature_type":"variation","strand":1,"end":140531262,"alleles":["C","G","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531264,"feature_type":"variation","strand":1,"end":140531264,"alleles":["A","C"],"clinical_significance":[],"id":"rs905394329","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796254155","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140531266,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531266},{"alleles":["C","A"],"end":140531270,"feature_type":"variation","strand":1,"source":"dbSNP","start":140531270,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs543207202"},{"seq_region_name":"7","id":"rs1796254371","clinical_significance":[],"alleles":["A","G"],"end":140531271,"strand":1,"feature_type":"variation","start":140531271,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140531272,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140531272,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1243490592","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796254548","clinical_significance":[],"start":140531281,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140531281,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1796254646","seq_region_name":"7","source":"dbSNP","start":140531282,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140531282,"alleles":["G","A"],"feature_type":"variation","strand":1},{"end":140531283,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140531283,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs771653661","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140531285,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531285,"source":"dbSNP","seq_region_name":"7","id":"rs1796254838","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140531286,"alleles":["G","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531286,"clinical_significance":[],"seq_region_name":"7","id":"rs1445518152"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796255077","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531288,"feature_type":"variation","strand":1,"end":140531288,"alleles":["G","-"]},{"strand":1,"feature_type":"variation","end":140531291,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531291,"source":"dbSNP","seq_region_name":"7","id":"rs887386011","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs945810630","end":140531293,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140531293,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1796255550","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531294,"source":"dbSNP","strand":1,"feature_type":"variation","end":140531294,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs977165512","clinical_significance":[],"end":140531295,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140531295,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1796255690","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531296,"source":"dbSNP","strand":1,"feature_type":"variation","end":140531296,"alleles":["G","A"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531299,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140531299,"id":"rs2130481031","seq_region_name":"7","clinical_significance":[]},{"start":140531302,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140531302,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1249123122","clinical_significance":[]},{"clinical_significance":[],"id":"rs1225990538","seq_region_name":"7","source":"dbSNP","start":140531306,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140531306,"alleles":["C","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796256054","source":"dbSNP","start":140531307,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140531307,"alleles":["A","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs2130481071","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531313,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140531313},{"alleles":["G","C"],"end":140531315,"strand":1,"feature_type":"variation","start":140531315,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1335104686","seq_region_name":"7","clinical_significance":[]},{"id":"rs1294705231","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140531326,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531326,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1412753071","end":140531329,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140531329,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140531330,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140531330,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs10237118"},{"id":"rs1171147004","seq_region_name":"7","clinical_significance":[],"start":140531333,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140531333,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"alleles":["C","T"],"end":140531336,"strand":1,"feature_type":"variation","start":140531336,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs2130481133","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140531339,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531339,"clinical_significance":[],"seq_region_name":"7","id":"rs1796256941"},{"end":140531343,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140531343,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796257044","clinical_significance":[]},{"alleles":["G","C"],"end":140531344,"strand":1,"feature_type":"variation","start":140531344,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1796257138","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531345,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140531345,"clinical_significance":[],"seq_region_name":"7","id":"rs1369282729"},{"seq_region_name":"7","id":"rs1393068031","clinical_significance":[],"end":140531346,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140531346,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs938513421","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531349,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140531349},{"source":"dbSNP","start":140531356,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140531356,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs965695402"},{"source":"dbSNP","start":140531360,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140531360,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1796257572","seq_region_name":"7"},{"seq_region_name":"7","id":"rs186463245","clinical_significance":[],"alleles":["C","A"],"end":140531361,"strand":1,"feature_type":"variation","start":140531361,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140531366,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531366,"source":"dbSNP","seq_region_name":"7","id":"rs2130481217","clinical_significance":[]},{"source":"dbSNP","start":140531378,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140531378,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1796257778","seq_region_name":"7"},{"seq_region_name":"7","id":"rs997307343","clinical_significance":[],"start":140531381,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140531381,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs894397520","clinical_significance":[],"strand":1,"feature_type":"variation","end":140531385,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531385,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130481248","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140531387,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531387},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796258077","source":"dbSNP","start":140531388,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140531388,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796258173","source":"dbSNP","start":140531389,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140531389,"alleles":["C","T"],"feature_type":"variation","strand":1},{"alleles":["C","A"],"end":140531390,"strand":1,"feature_type":"variation","start":140531390,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796258277","clinical_significance":[]},{"seq_region_name":"7","id":"rs931190425","clinical_significance":[],"end":140531391,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140531391,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531395,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140531395,"clinical_significance":[],"seq_region_name":"7","id":"rs1475119511"},{"source":"dbSNP","start":140531396,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C","G"],"end":140531396,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1331144700"},{"id":"rs1585562336","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140531400,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531400,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1796258758","clinical_significance":[],"strand":1,"feature_type":"variation","end":140531407,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531407,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1796258853","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140531416,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531416,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1383960064","clinical_significance":[],"alleles":["G","T"],"end":140531419,"strand":1,"feature_type":"variation","start":140531419,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140531424,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140531424,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs145053164","clinical_significance":[]},{"start":140531425,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140531425,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1436597313","clinical_significance":[]},{"end":140531436,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140531436,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs887777132","clinical_significance":[]},{"source":"dbSNP","start":140531437,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140531437,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130481378"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1250377042","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140531440,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531440},{"clinical_significance":[],"seq_region_name":"7","id":"rs568606352","feature_type":"variation","strand":1,"end":140531442,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531442},{"start":140531443,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140531443,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs953077374","clinical_significance":[]},{"start":140531446,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140531446,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585562394","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140531448,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531448,"clinical_significance":[],"seq_region_name":"7","id":"rs1274722056"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531455,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140531455,"seq_region_name":"7","id":"rs2130481426","clinical_significance":[]},{"start":140531462,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140531462,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs1796259964","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796260125","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531465,"source":"dbSNP","strand":1,"feature_type":"variation","end":140531465,"alleles":["A","G"]},{"id":"rs1585562404","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140531471,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531471,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140531472,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531472,"source":"dbSNP","seq_region_name":"7","id":"rs1014948801","clinical_significance":[]},{"source":"dbSNP","start":140531473,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140531473,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796260433"},{"feature_type":"variation","strand":1,"end":140531474,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531474,"clinical_significance":[],"id":"rs559471052","seq_region_name":"7"},{"end":140531476,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140531476,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1333612164"},{"seq_region_name":"7","id":"rs1279937223","clinical_significance":[],"alleles":["T","G"],"end":140531477,"strand":1,"feature_type":"variation","start":140531477,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130481502","feature_type":"variation","strand":1,"end":140531482,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531482},{"seq_region_name":"7","id":"rs866573979","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140531484,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531484,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs111931753","end":140531485,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140531485,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1796261124","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140531490,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531490,"source":"dbSNP"},{"end":140531493,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140531493,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1333938798"},{"alleles":["C","G"],"end":140531494,"strand":1,"feature_type":"variation","start":140531494,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs375287951","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140531503,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140531503,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1328061739"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531504,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CTATCT","CT"],"end":140531509,"id":"rs1796261497","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs997712878","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531507,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140531507},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796261702","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531507,"feature_type":"variation","strand":1,"end":140531509,"alleles":["TCT","T"]},{"end":140531508,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140531508,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs768105625"},{"clinical_significance":[],"id":"rs956657273","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531510,"feature_type":"variation","strand":1,"end":140531510,"alleles":["G","A"]},{"alleles":["T","C"],"end":140531515,"feature_type":"variation","strand":1,"source":"dbSNP","start":140531515,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs988455712","seq_region_name":"7"},{"seq_region_name":"7","id":"rs2130481613","clinical_significance":[],"start":140531516,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140531516,"strand":1,"feature_type":"variation"},{"alleles":["C","A","T"],"end":140531520,"strand":1,"feature_type":"variation","start":140531520,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs868702243","clinical_significance":[]},{"clinical_significance":[],"id":"rs1029536113","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531521,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140531521},{"seq_region_name":"7","id":"rs1363770179","clinical_significance":[],"start":140531522,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140531522,"strand":1,"feature_type":"variation"},{"id":"rs1197903717","seq_region_name":"7","clinical_significance":[],"start":140531526,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140531526,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1468583493","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140531527,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531527,"source":"dbSNP"},{"source":"dbSNP","start":140531528,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140531528,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs917955509"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1211209820","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531529,"feature_type":"variation","strand":1,"end":140531529,"alleles":["T","C"]},{"id":"rs1263586626","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140531532,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531532,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1796263236","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531533,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140531533},{"seq_region_name":"7","id":"rs181754292","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140531534,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531534,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1011826665","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531535,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140531535},{"strand":1,"feature_type":"variation","end":140531548,"alleles":["CCTGTAATCCT","CCT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531538,"source":"dbSNP","seq_region_name":"7","id":"rs1284470808","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531547,"feature_type":"variation","strand":1,"end":140531547,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1796263823"},{"id":"rs536903413","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531551,"source":"dbSNP","strand":1,"feature_type":"variation","end":140531551,"alleles":["C","A"]},{"seq_region_name":"7","id":"rs1348246289","clinical_significance":[],"strand":1,"feature_type":"variation","end":140531553,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531553,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531558,"feature_type":"variation","strand":1,"end":140531558,"alleles":["G","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1235951791"},{"seq_region_name":"7","id":"rs777171584","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531561,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140531561},{"source":"dbSNP","start":140531569,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140531569,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs754296297"},{"source":"dbSNP","start":140531570,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140531570,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796264748"},{"clinical_significance":[],"id":"rs1301356902","seq_region_name":"7","source":"dbSNP","start":140531571,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140531575,"alleles":["GGTGG","GG"],"feature_type":"variation","strand":1},{"end":140531573,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140531573,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs937628017","seq_region_name":"7"},{"id":"rs2130481845","seq_region_name":"7","clinical_significance":[],"start":140531574,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140531574,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1346048617","clinical_significance":[],"start":140531581,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140531581,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1320501706","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531585,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140531585},{"clinical_significance":[],"seq_region_name":"7","id":"rs1399375669","source":"dbSNP","start":140531588,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140531588,"alleles":["C","T"],"feature_type":"variation","strand":1},{"alleles":["A","G"],"end":140531589,"strand":1,"feature_type":"variation","start":140531589,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796265720","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs540778665","end":140531591,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140531591,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1421691617","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531591,"source":"dbSNP","strand":1,"feature_type":"variation","end":140531593,"alleles":["GAG","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1427310179","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531597,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140531597},{"clinical_significance":[],"id":"rs1796266392","seq_region_name":"7","end":140531597,"alleles":["-","GATC"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140531598,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["G","A"],"end":140531599,"strand":1,"feature_type":"variation","start":140531599,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs549257773","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531600,"feature_type":"variation","strand":1,"alleles":["-","ATCA"],"end":140531599,"clinical_significance":[],"id":"rs1455974444","seq_region_name":"7"},{"end":140531602,"alleles":["GCT","-"],"strand":1,"feature_type":"variation","start":140531600,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1796266860","seq_region_name":"7","clinical_significance":[]},{"id":"rs1393755984","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531602,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TATA","-"],"end":140531605},{"seq_region_name":"7","id":"rs1407383827","clinical_significance":[],"start":140531604,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140531604,"strand":1,"feature_type":"variation"},{"id":"rs1796267244","seq_region_name":"7","clinical_significance":[],"start":140531606,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140531606,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140531609,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531609,"source":"dbSNP","seq_region_name":"7","id":"rs567390661","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140531613,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531613,"clinical_significance":[],"id":"rs1796267642","seq_region_name":"7"},{"end":140531619,"alleles":["A","G","T"],"strand":1,"feature_type":"variation","start":140531619,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs10243343","clinical_significance":[]},{"end":140531626,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140531626,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1335069077","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs10237487","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531627,"feature_type":"variation","strand":1,"end":140531627,"alleles":["C","A","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531628,"source":"dbSNP","strand":1,"feature_type":"variation","end":140531628,"alleles":["G","A"],"seq_region_name":"7","id":"rs931365134","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531635,"source":"dbSNP","strand":1,"feature_type":"variation","end":140531635,"alleles":["C","A"],"id":"rs1211263347","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531637,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140531637,"clinical_significance":[],"seq_region_name":"7","id":"rs10243349"},{"source":"dbSNP","start":140531637,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140531637,"alleles":["A","ACAAATACAA"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796268879"},{"alleles":["AAAAATACAAAAAATACAAAAA","AAAAATACAAAAA"],"end":140531658,"strand":1,"feature_type":"variation","start":140531637,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1048560780","clinical_significance":[]},{"end":140531638,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140531638,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1796269205","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531640,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140531640,"seq_region_name":"7","id":"rs1278056088","clinical_significance":[]},{"clinical_significance":[],"id":"rs1430954340","seq_region_name":"7","alleles":["A","C"],"end":140531641,"feature_type":"variation","strand":1,"source":"dbSNP","start":140531641,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs535920949","clinical_significance":[],"alleles":["A","G"],"end":140531643,"strand":1,"feature_type":"variation","start":140531643,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1796269807","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531651,"source":"dbSNP","strand":1,"feature_type":"variation","end":140531651,"alleles":["T","C"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531652,"feature_type":"variation","strand":1,"end":140531652,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1362728183"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531653,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140531653,"clinical_significance":[],"seq_region_name":"7","id":"rs1272211874"},{"alleles":["A","G"],"end":140531654,"feature_type":"variation","strand":1,"source":"dbSNP","start":140531654,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs928424686","seq_region_name":"7"},{"start":140531655,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140531655,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs960021845","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796270519","end":140531658,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140531658,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140531660,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140531660,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796270661"},{"seq_region_name":"7","id":"rs1359232963","clinical_significance":[],"start":140531660,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140531665,"alleles":["AAAAAA","AAAAA"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1796270955","clinical_significance":[],"start":140531661,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140531661,"strand":1,"feature_type":"variation"},{"start":140531664,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140531664,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796271061","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1313889749","alleles":["C","A","T"],"end":140531666,"feature_type":"variation","strand":1,"source":"dbSNP","start":140531666,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1004504821","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140531667,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531667,"source":"dbSNP"},{"id":"rs1796271528","seq_region_name":"7","clinical_significance":[],"alleles":["G","A","C"],"end":140531669,"strand":1,"feature_type":"variation","start":140531669,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531671,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140531671,"seq_region_name":"7","id":"rs762189543","clinical_significance":[]},{"id":"rs1325515633","seq_region_name":"7","clinical_significance":[],"start":140531672,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140531672,"alleles":["G","A","T"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140531675,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140531675,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs915723611","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140531676,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531676,"source":"dbSNP","id":"rs931286123","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531678,"source":"dbSNP","strand":1,"feature_type":"variation","end":140531678,"alleles":["G","C"],"seq_region_name":"7","id":"rs901536374","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796272471","clinical_significance":[],"start":140531679,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140531679,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"end":140531680,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140531680,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs997196147","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1028637245","end":140531681,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140531681,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140531682,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140531682,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1241109720"},{"clinical_significance":[],"seq_region_name":"7","id":"rs754498739","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531683,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140531683},{"seq_region_name":"7","id":"rs186426223","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140531684,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531684,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs577679863","feature_type":"variation","strand":1,"end":140531686,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531686},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531687,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140531687,"id":"rs1000989082","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140531688,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531688,"clinical_significance":[],"seq_region_name":"7","id":"rs1796273755"},{"alleles":["C","T"],"end":140531689,"feature_type":"variation","strand":1,"source":"dbSNP","start":140531689,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1032210424"},{"seq_region_name":"7","id":"rs1307933768","clinical_significance":[],"end":140531690,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140531690,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["T","G"],"end":140531691,"strand":1,"feature_type":"variation","start":140531691,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796274249","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140531694,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531694,"clinical_significance":[],"seq_region_name":"7","id":"rs1277595357"},{"clinical_significance":[],"id":"rs1048282528","seq_region_name":"7","alleles":["A","T"],"end":140531695,"feature_type":"variation","strand":1,"source":"dbSNP","start":140531695,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531697,"source":"dbSNP","strand":1,"feature_type":"variation","end":140531697,"alleles":["C","A"],"id":"rs1796274692","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796274832","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140531698,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531698},{"id":"rs909246618","seq_region_name":"7","clinical_significance":[],"start":140531706,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140531706,"strand":1,"feature_type":"variation"},{"start":140531707,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140531707,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796275101","clinical_significance":[]},{"start":140531713,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C"],"end":140531713,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1442092999","clinical_significance":[]},{"end":140531725,"alleles":["GAGGCAGGAG","GAG"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140531716,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1216741994","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1212826149","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531718,"source":"dbSNP","strand":1,"feature_type":"variation","end":140531718,"alleles":["G","A","C"]},{"end":140531719,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140531719,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1339015572"},{"strand":1,"feature_type":"variation","end":140531726,"alleles":["A","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531726,"source":"dbSNP","id":"rs368355737","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1243975325","clinical_significance":[],"start":140531729,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140531729,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs538656228","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140531730,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531730,"source":"dbSNP"},{"source":"dbSNP","start":140531731,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140531731,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs940709044"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130482419","alleles":["G","A"],"end":140531734,"feature_type":"variation","strand":1,"source":"dbSNP","start":140531734,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140531737,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531737,"clinical_significance":[],"id":"rs765797444","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531738,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140531738,"clinical_significance":[],"seq_region_name":"7","id":"rs1443571150"},{"source":"dbSNP","start":140531743,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140531743,"alleles":["A","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1356730398"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531746,"feature_type":"variation","strand":1,"end":140531746,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs901929219"},{"start":140531747,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140531747,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1487346030","clinical_significance":[]},{"clinical_significance":[],"id":"rs149116929","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531750,"feature_type":"variation","strand":1,"end":140531750,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585563159","end":140531752,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140531752,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531754,"source":"dbSNP","strand":1,"feature_type":"variation","end":140531754,"alleles":["G","A"],"seq_region_name":"7","id":"rs1796277798","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796277942","clinical_significance":[],"alleles":["A","G"],"end":140531760,"strand":1,"feature_type":"variation","start":140531760,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140531763,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531763,"clinical_significance":[],"id":"rs575663626","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531764,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140531764,"seq_region_name":"7","id":"rs889279546","clinical_significance":[]},{"alleles":["A","T"],"end":140531768,"strand":1,"feature_type":"variation","start":140531768,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1255138127","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs191190308","alleles":["C","A","T"],"end":140531771,"feature_type":"variation","strand":1,"source":"dbSNP","start":140531771,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531772,"feature_type":"variation","strand":1,"end":140531772,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1796278775"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796278911","source":"dbSNP","start":140531773,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140531773,"feature_type":"variation","strand":1},{"end":140531776,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140531776,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1563120924","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796279207","clinical_significance":[],"start":140531777,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140531777,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["C","A","G"],"end":140531781,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531781,"source":"dbSNP","seq_region_name":"7","id":"rs1796279353","clinical_significance":[]},{"seq_region_name":"7","id":"rs1171218661","clinical_significance":[],"strand":1,"feature_type":"variation","end":140531782,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531782,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs561608790","source":"dbSNP","start":140531783,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140531783,"alleles":["C","T"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140531785,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140531785,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130482606"},{"strand":1,"feature_type":"variation","end":140531786,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531786,"source":"dbSNP","id":"rs1480929214","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140531790,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531790,"source":"dbSNP","id":"rs1796279912","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140531800,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140531800,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs763415970","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs182237254","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140531801,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531801},{"seq_region_name":"7","id":"rs778331557","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531802,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140531802},{"seq_region_name":"7","id":"rs926586774","clinical_significance":[],"alleles":["C","CC"],"end":140531802,"strand":1,"feature_type":"variation","start":140531802,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1235362328","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531803,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140531803},{"end":140531804,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140531804,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs998526947","clinical_significance":[]},{"source":"dbSNP","start":140531805,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140531805,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs115257324"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1224637035","source":"dbSNP","start":140531807,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140531807,"alleles":["C","T"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140531809,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531809,"source":"dbSNP","id":"rs1796281098","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796281212","source":"dbSNP","start":140531810,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140531810,"alleles":["T","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs959852402","seq_region_name":"7","source":"dbSNP","start":140531812,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140531812,"alleles":["T","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1296928037","clinical_significance":[],"alleles":["C","T"],"end":140531815,"strand":1,"feature_type":"variation","start":140531815,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1796281572","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531819,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140531819},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585563316","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140531822,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531822},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531823,"source":"dbSNP","strand":1,"feature_type":"variation","end":140531823,"alleles":["A","AGCAACA"],"seq_region_name":"7","id":"rs111481676","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs60323045","end":140531845,"alleles":["AACAACAACAACAACAACAACAA","AACAACAACAACAACAA","AACAACAACAACAACAACAA","AACAACAACAACAACAACAACAACAA","AACAACAACAACAACAACAACAACAACAA","AACAACAACAACAACAACAACAACAACAACAA","AACAACAACAACAACAACAACAACAACAACAACAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140531823,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796282497","feature_type":"variation","strand":1,"end":140531824,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531824},{"source":"dbSNP","start":140531824,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AC","ACGAC"],"end":140531825,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796282621"},{"clinical_significance":[],"seq_region_name":"7","id":"rs34980972","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531826,"feature_type":"variation","strand":1,"alleles":["-","CAA"],"end":140531825},{"start":140531830,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AC","ACGAC"],"end":140531831,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796282919","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531846,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["-","C","CAACAC","CAC"],"end":140531845,"id":"rs1554460292","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1410134538","seq_region_name":"7","alleles":["A","C"],"end":140531846,"feature_type":"variation","strand":1,"source":"dbSNP","start":140531846,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1175396856","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140531847,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531847},{"clinical_significance":[],"seq_region_name":"7","id":"rs1439235430","source":"dbSNP","start":140531848,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140531848,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1796283540","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531851,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140531851},{"strand":1,"feature_type":"variation","alleles":["CTATCT","CT"],"end":140531856,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531851,"source":"dbSNP","id":"rs1796283630","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","-"],"end":140531852,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531852,"source":"dbSNP","id":"rs1253709825","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796283737","clinical_significance":[],"strand":1,"feature_type":"variation","end":140531852,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531852,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1215575768","end":140531854,"alleles":["T","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140531854,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796284056","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531855,"feature_type":"variation","strand":1,"end":140531855,"alleles":["C","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796284165","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531856,"feature_type":"variation","strand":1,"alleles":["TGTGTGTGTG","TGTGTGTG"],"end":140531865},{"seq_region_name":"7","id":"rs1272737985","clinical_significance":[],"start":140531857,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140531857,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1205814840","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531864,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140531864},{"strand":1,"feature_type":"variation","end":140531867,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531867,"source":"dbSNP","seq_region_name":"7","id":"rs1796284437","clinical_significance":[]},{"seq_region_name":"7","id":"rs1252581326","clinical_significance":[],"end":140531870,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140531870,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796284629","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531871,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140531871},{"seq_region_name":"7","id":"rs372349078","clinical_significance":[],"start":140531873,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G","T"],"end":140531873,"strand":1,"feature_type":"variation"},{"end":140531874,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140531874,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1305570040"},{"strand":1,"feature_type":"variation","end":140531877,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531877,"source":"dbSNP","seq_region_name":"7","id":"rs1585563478","clinical_significance":[]},{"source":"dbSNP","start":140531883,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140531883,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1303172811","seq_region_name":"7"},{"source":"dbSNP","start":140531886,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140531886,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs915770729"},{"feature_type":"variation","strand":1,"end":140531887,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531887,"clinical_significance":[],"id":"rs559507771","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs751892092","source":"dbSNP","start":140531889,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140531889,"alleles":["C","T"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140531890,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140531890,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796285500"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1303530716","alleles":["G","C"],"end":140531894,"feature_type":"variation","strand":1,"source":"dbSNP","start":140531894,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs983890888","seq_region_name":"7","feature_type":"variation","strand":1,"end":140531895,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531895},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796285770","feature_type":"variation","strand":1,"alleles":["G","-"],"end":140531899,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531899},{"clinical_significance":[],"seq_region_name":"7","id":"rs533021348","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531901,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140531901},{"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140531903,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531903,"source":"dbSNP","seq_region_name":"7","id":"rs755066082","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","TT"],"end":140531904,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531904,"clinical_significance":[],"seq_region_name":"7","id":"rs1796286092"},{"seq_region_name":"7","id":"rs2130483052","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531907,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140531907},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531911,"source":"dbSNP","strand":1,"feature_type":"variation","end":140531911,"alleles":["T","C"],"seq_region_name":"7","id":"rs932847969","clinical_significance":[]},{"alleles":["G","A"],"end":140531912,"strand":1,"feature_type":"variation","start":140531912,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs2130483079","seq_region_name":"7","clinical_significance":[]},{"end":140531915,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140531915,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796286403"},{"seq_region_name":"7","id":"rs1796286546","clinical_significance":[],"start":140531918,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140531918,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"end":140531922,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140531922,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1274071131","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1156585100","source":"dbSNP","start":140531928,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140531928,"alleles":["T","A","C"],"feature_type":"variation","strand":1},{"start":140531929,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140531929,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1050094332","clinical_significance":[]},{"seq_region_name":"7","id":"rs888770666","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531930,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140531930},{"seq_region_name":"7","id":"rs1796287449","clinical_significance":[],"start":140531935,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140531935,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140531936,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140531936,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1195612420"},{"feature_type":"variation","strand":1,"end":140531950,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531950,"clinical_significance":[],"seq_region_name":"7","id":"rs1563121019"},{"strand":1,"feature_type":"variation","end":140531951,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531951,"source":"dbSNP","seq_region_name":"7","id":"rs1452625251","clinical_significance":[]},{"end":140531952,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140531952,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130483173","clinical_significance":[]},{"seq_region_name":"7","id":"rs1000659519","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531955,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140531955},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531957,"feature_type":"variation","strand":1,"end":140531957,"alleles":["T","C"],"clinical_significance":[],"id":"rs1187321716","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796288155","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140531971,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531971},{"id":"rs1796288279","seq_region_name":"7","clinical_significance":[],"alleles":["G","T"],"end":140531972,"strand":1,"feature_type":"variation","start":140531972,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1487094699","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531978,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140531978},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796288522","source":"dbSNP","start":140531981,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140531981,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs908486207","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531982,"feature_type":"variation","strand":1,"end":140531982,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796288722","source":"dbSNP","start":140531983,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140531983,"feature_type":"variation","strand":1},{"start":140531987,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140531987,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs939901403","clinical_significance":[]},{"id":"rs1032487727","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140531990,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140531990,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1351706590","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140531992,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140531992},{"seq_region_name":"7","id":"rs1215453865","clinical_significance":[],"alleles":["C","T"],"end":140532000,"strand":1,"feature_type":"variation","start":140532000,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532001,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","G"],"end":140532001,"seq_region_name":"7","id":"rs11977004","clinical_significance":[]},{"id":"rs368529789","seq_region_name":"7","clinical_significance":[],"start":140532006,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140532006,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140532010,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140532010,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs923256500"},{"alleles":["C","T"],"end":140532012,"feature_type":"variation","strand":1,"source":"dbSNP","start":140532012,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs371016924"},{"clinical_significance":[],"seq_region_name":"7","id":"rs4421283","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532025,"feature_type":"variation","strand":1,"end":140532025,"alleles":["A","G"]},{"end":140532028,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140532028,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796289850"},{"id":"rs1269645214","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140532029,"strand":1,"feature_type":"variation","start":140532029,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1796290052","seq_region_name":"7","alleles":["G","C"],"end":140532031,"feature_type":"variation","strand":1,"source":"dbSNP","start":140532031,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs563321220","clinical_significance":[],"start":140532032,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140532032,"strand":1,"feature_type":"variation"},{"end":140532033,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140532033,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1286925433"},{"id":"rs4421284","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140532034,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532034,"source":"dbSNP"},{"id":"rs185421449","seq_region_name":"7","clinical_significance":[],"alleles":["G","A","C","T"],"end":140532036,"strand":1,"feature_type":"variation","start":140532036,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1585563755","clinical_significance":[],"end":140532037,"alleles":["T","C","G"],"strand":1,"feature_type":"variation","start":140532037,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140532038,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532038,"source":"dbSNP","seq_region_name":"7","id":"rs4421285","clinical_significance":[]},{"end":140532038,"alleles":["A","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140532038,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1197339339"},{"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140532040,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532040,"source":"dbSNP","seq_region_name":"7","id":"rs549043346","clinical_significance":[]},{"seq_region_name":"7","id":"rs1377139849","clinical_significance":[],"end":140532045,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140532045,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["CTGAGGTC","C"],"end":140532052,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532045,"clinical_significance":[],"seq_region_name":"7","id":"rs1796291307"},{"seq_region_name":"7","id":"rs1796291405","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140532049,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532049,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1796291509","clinical_significance":[],"end":140532052,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140532052,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140532060,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532060,"source":"dbSNP","seq_region_name":"7","id":"rs567523975","clinical_significance":[]},{"id":"rs1430540045","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140532061,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532061,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532062,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140532062,"seq_region_name":"7","id":"rs1796291786","clinical_significance":[]},{"alleles":["T","C"],"end":140532065,"feature_type":"variation","strand":1,"source":"dbSNP","start":140532065,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796291878"},{"clinical_significance":[],"seq_region_name":"7","id":"rs528290951","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532067,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140532067},{"source":"dbSNP","start":140532070,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140532070,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130483463"},{"start":140532071,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140532071,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1024741724","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796292197","source":"dbSNP","start":140532073,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140532073,"alleles":["G","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1796292290","clinical_significance":[],"end":140532077,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140532077,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs546347412","feature_type":"variation","strand":1,"end":140532079,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532079},{"clinical_significance":[],"seq_region_name":"7","id":"rs1260298728","source":"dbSNP","start":140532082,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140532082,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140532084,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532084,"clinical_significance":[],"seq_region_name":"7","id":"rs1378115511"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796292720","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532088,"feature_type":"variation","strand":1,"alleles":["CCC","CC"],"end":140532090},{"seq_region_name":"7","id":"rs2130483530","clinical_significance":[],"end":140532091,"alleles":["CT","-"],"strand":1,"feature_type":"variation","start":140532090,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796292801","end":140532093,"alleles":["TGT","TGTGT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140532091,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140532093,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C","G"],"end":140532093,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796292888","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532099,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140532099,"clinical_significance":[],"id":"rs1796292991","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796293088","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532100,"feature_type":"variation","strand":1,"end":140532100,"alleles":["T","C"]},{"id":"rs1344842994","seq_region_name":"7","clinical_significance":[],"start":140532105,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140532105,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs571410253","alleles":["A","G"],"end":140532109,"feature_type":"variation","strand":1,"source":"dbSNP","start":140532109,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532109,"feature_type":"variation","strand":1,"alleles":["AAAAAAA","AAAAAA"],"end":140532115,"clinical_significance":[],"seq_region_name":"7","id":"rs2130483588"},{"clinical_significance":[],"id":"rs538793068","seq_region_name":"7","alleles":["A","G"],"end":140532115,"feature_type":"variation","strand":1,"source":"dbSNP","start":140532115,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532116,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140532116,"seq_region_name":"7","id":"rs1796293423","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130483622","clinical_significance":[],"start":140532125,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TGTG","TG"],"end":140532128,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532132,"source":"dbSNP","strand":1,"feature_type":"variation","end":140532132,"alleles":["G","A"],"seq_region_name":"7","id":"rs142246407","clinical_significance":[]},{"seq_region_name":"7","id":"rs903446580","clinical_significance":[],"alleles":["C","T"],"end":140532133,"strand":1,"feature_type":"variation","start":140532133,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs189923241","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532134,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140532134},{"seq_region_name":"7","id":"rs1796293739","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140532135,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532135,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1308925427","clinical_significance":[],"alleles":["G","A"],"end":140532136,"strand":1,"feature_type":"variation","start":140532136,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140532137,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532137,"source":"dbSNP","seq_region_name":"7","id":"rs952821312","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585563928","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140532139,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532139},{"source":"dbSNP","start":140532140,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140532140,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1366861296"},{"clinical_significance":[],"id":"rs1796294190","seq_region_name":"7","end":140532145,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140532145,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs2130483714","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532151,"feature_type":"variation","strand":1,"end":140532151,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1796294275","clinical_significance":[],"start":140532152,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140532152,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1355843206","alleles":["T","C"],"end":140532153,"feature_type":"variation","strand":1,"source":"dbSNP","start":140532153,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1314743008","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532157,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140532157},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532158,"source":"dbSNP","strand":1,"feature_type":"variation","end":140532158,"alleles":["G","A"],"id":"rs1412869020","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532158,"feature_type":"variation","strand":1,"alleles":["GGGAGGGAGG","GGGAGG"],"end":140532167,"clinical_significance":[],"seq_region_name":"7","id":"rs1796294661"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585563983","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532159,"feature_type":"variation","strand":1,"end":140532159,"alleles":["G","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585563992","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532161,"feature_type":"variation","strand":1,"end":140532161,"alleles":["A","G"]},{"clinical_significance":[],"id":"rs1796294920","seq_region_name":"7","alleles":["G","A"],"end":140532162,"feature_type":"variation","strand":1,"source":"dbSNP","start":140532162,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs376784660","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140532163,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532163},{"strand":1,"feature_type":"variation","end":140532166,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532166,"source":"dbSNP","id":"rs1796295098","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532167,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140532167,"clinical_significance":[],"id":"rs1796295172","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1298846842","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532169,"feature_type":"variation","strand":1,"end":140532169,"alleles":["T","G"]},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140532176,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532176,"source":"dbSNP","seq_region_name":"7","id":"rs1796295350","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585564028","clinical_significance":[],"alleles":["G","A"],"end":140532177,"strand":1,"feature_type":"variation","start":140532177,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532181,"source":"dbSNP","strand":1,"feature_type":"variation","end":140532181,"alleles":["A","C"],"seq_region_name":"7","id":"rs1463561265","clinical_significance":[]},{"alleles":["C","T"],"end":140532183,"strand":1,"feature_type":"variation","start":140532183,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1371602867","clinical_significance":[]},{"id":"rs895454713","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532184,"source":"dbSNP","strand":1,"feature_type":"variation","end":140532184,"alleles":["G","A"]},{"end":140532187,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140532187,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796295728","clinical_significance":[]},{"end":140532193,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140532193,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1475776301"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532194,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140532194,"seq_region_name":"7","id":"rs1322806724","clinical_significance":[]},{"end":140532196,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140532196,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1186184069","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140532198,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532198,"source":"dbSNP","seq_region_name":"7","id":"rs1336206005","clinical_significance":[]},{"id":"rs1796296218","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140532200,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532200,"source":"dbSNP"},{"id":"rs1796296295","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140532205,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532205,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532205,"feature_type":"variation","strand":1,"alleles":["GTTGTTGT","GTTGT"],"end":140532212,"clinical_significance":[],"id":"rs2130483909","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140532207,"alleles":["TT","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532206,"clinical_significance":[],"seq_region_name":"7","id":"rs756218240"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796296486","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532208,"feature_type":"variation","strand":1,"end":140532208,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1195915850","alleles":["G","A"],"end":140532211,"feature_type":"variation","strand":1,"source":"dbSNP","start":140532211,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140532212,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532212,"clinical_significance":[],"seq_region_name":"7","id":"rs367709356"},{"clinical_significance":[],"seq_region_name":"7","id":"rs940062042","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140532225,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532225},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532226,"source":"dbSNP","strand":1,"feature_type":"variation","end":140532226,"alleles":["G","A"],"seq_region_name":"7","id":"rs113994315","clinical_significance":[]},{"start":140532230,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140532230,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130483976","clinical_significance":[]},{"id":"rs1335005895","seq_region_name":"7","clinical_significance":[],"start":140532231,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140532231,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140532234,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532234,"clinical_significance":[],"id":"rs2130484009","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1294923605","clinical_significance":[],"strand":1,"feature_type":"variation","end":140532237,"alleles":["C","A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532237,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1796297164","clinical_significance":[],"start":140532240,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140532240,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140532245,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140532245,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs541655981"},{"seq_region_name":"7","id":"rs1796297356","clinical_significance":[],"end":140532250,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140532250,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs746807568","feature_type":"variation","strand":1,"alleles":["AGAG","AG"],"end":140532254,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532251},{"seq_region_name":"7","id":"rs375303977","clinical_significance":[],"start":140532253,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140532253,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140532260,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532260,"source":"dbSNP","seq_region_name":"7","id":"rs1329427027","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140532263,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532263,"clinical_significance":[],"seq_region_name":"7","id":"rs183122988"},{"end":140532264,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140532264,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs779666982"},{"alleles":["T","C"],"end":140532265,"feature_type":"variation","strand":1,"source":"dbSNP","start":140532265,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs10250728"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532268,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140532268,"clinical_significance":[],"seq_region_name":"7","id":"rs1796298105"},{"seq_region_name":"7","id":"rs1396900903","clinical_significance":[],"start":140532269,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140532269,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["AAAAAAA","AAAAAAAA","AAAAAAAAA"],"end":140532275,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532269,"source":"dbSNP","seq_region_name":"7","id":"rs1184454579","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1236689027","source":"dbSNP","start":140532271,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140532271,"alleles":["A","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs530758321","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532272,"source":"dbSNP","strand":1,"feature_type":"variation","end":140532272,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs1796298574","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532277,"source":"dbSNP","strand":1,"feature_type":"variation","end":140532277,"alleles":["A","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs936320224","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532277,"feature_type":"variation","strand":1,"alleles":["AAAA","AA"],"end":140532280},{"strand":1,"feature_type":"variation","end":140532278,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532278,"source":"dbSNP","id":"rs1364931009","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1184586938","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532279,"feature_type":"variation","strand":1,"end":140532279,"alleles":["A","C","G"]},{"clinical_significance":[],"id":"rs923318513","seq_region_name":"7","end":140532280,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140532280,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532287,"feature_type":"variation","strand":1,"alleles":["TT","TTT"],"end":140532288,"clinical_significance":[],"seq_region_name":"7","id":"rs1420428826"},{"start":140532290,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140532290,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1183799717","clinical_significance":[]},{"end":140532297,"alleles":["A","G","T"],"strand":1,"feature_type":"variation","start":140532297,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1235836911","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796299335","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532300,"feature_type":"variation","strand":1,"end":140532300,"alleles":["C","A"]},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140532304,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532304,"clinical_significance":[],"seq_region_name":"7","id":"rs1796299425"},{"seq_region_name":"7","id":"rs1796299523","clinical_significance":[],"end":140532305,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140532305,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140532306,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140532306,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796299613"},{"id":"rs540498445","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140532307,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532307,"source":"dbSNP"},{"source":"dbSNP","start":140532308,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140532308,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796299837"},{"id":"rs1053428736","seq_region_name":"7","clinical_significance":[],"alleles":["A","G","T"],"end":140532314,"strand":1,"feature_type":"variation","start":140532314,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs2130484234","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532321,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140532321},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532322,"source":"dbSNP","strand":1,"feature_type":"variation","end":140532323,"alleles":["TG","TGTG"],"id":"rs1796300056","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1009233172","clinical_significance":[],"start":140532327,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140532327,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140532331,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532331,"source":"dbSNP","id":"rs1386626863","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1796300329","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532334,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140532334},{"strand":1,"feature_type":"variation","alleles":["TTTTT","TTT","TTTT"],"end":140532339,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532335,"source":"dbSNP","seq_region_name":"7","id":"rs1241101762","clinical_significance":[]},{"id":"rs1455936800","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140532339,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532339,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs933302245","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140532341,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532341},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532344,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140532344,"clinical_significance":[],"seq_region_name":"7","id":"rs1796300684"},{"alleles":["C","A","T"],"end":140532346,"strand":1,"feature_type":"variation","start":140532346,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs986117871","clinical_significance":[]},{"alleles":["G","A","C"],"end":140532347,"feature_type":"variation","strand":1,"source":"dbSNP","start":140532347,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs910655852","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1377350297","feature_type":"variation","strand":1,"end":140532354,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532354},{"feature_type":"variation","strand":1,"end":140532355,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532355,"clinical_significance":[],"seq_region_name":"7","id":"rs1386132841"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796301223","source":"dbSNP","start":140532359,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140532359,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1160592366","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140532362,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532362},{"alleles":["G","-"],"end":140532367,"strand":1,"feature_type":"variation","start":140532367,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1397152092","clinical_significance":[]},{"alleles":["G","T"],"end":140532369,"feature_type":"variation","strand":1,"source":"dbSNP","start":140532369,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs770708153","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532372,"source":"dbSNP","strand":1,"feature_type":"variation","end":140532372,"alleles":["T","G"],"seq_region_name":"7","id":"rs1796301613","clinical_significance":[]},{"start":140532373,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140532373,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs1329092027","seq_region_name":"7","clinical_significance":[]},{"id":"rs1796301799","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532374,"source":"dbSNP","strand":1,"feature_type":"variation","end":140532374,"alleles":["G","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796301890","alleles":["A","G"],"end":140532377,"feature_type":"variation","strand":1,"source":"dbSNP","start":140532377,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140532379,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140532379,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs540840917"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796302073","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532383,"feature_type":"variation","strand":1,"end":140532383,"alleles":["G","A"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532384,"feature_type":"variation","strand":1,"end":140532384,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1043281906"},{"clinical_significance":[],"id":"rs1796302244","seq_region_name":"7","alleles":["G","A"],"end":140532385,"feature_type":"variation","strand":1,"source":"dbSNP","start":140532385,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1796302320","clinical_significance":[],"strand":1,"feature_type":"variation","end":140532387,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532387,"source":"dbSNP"},{"source":"dbSNP","start":140532388,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140532387,"alleles":["-","GAC"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1446390825"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1177506846","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532388,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140532388},{"seq_region_name":"7","id":"rs1454313078","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532389,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140532389},{"id":"rs1315991909","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["CA","-"],"end":140532390,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532389,"source":"dbSNP"},{"start":140532390,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C","G"],"end":140532390,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs903351732","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs559148636","feature_type":"variation","strand":1,"end":140532391,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532391},{"clinical_significance":[],"id":"rs1450615447","seq_region_name":"7","feature_type":"variation","strand":1,"end":140532391,"alleles":["-","TG"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532392},{"clinical_significance":[],"id":"rs1563121280","seq_region_name":"7","source":"dbSNP","start":140532392,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140532392,"alleles":["G","GG"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1284706798","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532393,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140532393},{"clinical_significance":[],"seq_region_name":"7","id":"rs1206623096","source":"dbSNP","start":140532396,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140532396,"alleles":["A","C"],"feature_type":"variation","strand":1},{"id":"rs1385180093","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532397,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140532397},{"start":140532399,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140532399,"alleles":["T","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1033998140","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532400,"feature_type":"variation","strand":1,"end":140532400,"alleles":["C","T"],"clinical_significance":[],"id":"rs1796303330","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532403,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140532403,"clinical_significance":[],"seq_region_name":"7","id":"rs1285182695"},{"alleles":["G","A","T"],"end":140532405,"feature_type":"variation","strand":1,"source":"dbSNP","start":140532405,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1242723062"},{"strand":1,"feature_type":"variation","end":140532413,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532413,"source":"dbSNP","seq_region_name":"7","id":"rs1796303616","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532418,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140532418,"clinical_significance":[],"seq_region_name":"7","id":"rs188010419"},{"seq_region_name":"7","id":"rs1796303811","clinical_significance":[],"alleles":["T","C"],"end":140532421,"strand":1,"feature_type":"variation","start":140532421,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532434,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140532434,"seq_region_name":"7","id":"rs984545543","clinical_significance":[]},{"end":140532437,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140532437,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130484612","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140532442,"alleles":["CC","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532441,"source":"dbSNP","id":"rs1198043213","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532442,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140532442,"clinical_significance":[],"id":"rs1436037841","seq_region_name":"7"},{"start":140532443,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140532443,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","id":"rs4726889","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796304448","clinical_significance":[],"start":140532447,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140532447,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1796304552","clinical_significance":[],"alleles":["G","A","T"],"end":140532449,"strand":1,"feature_type":"variation","start":140532449,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs6963769","clinical_significance":[],"start":140532451,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140532451,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140532456,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AAAAAA","AAAAAAA"],"end":140532461,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1320722623"},{"start":140532459,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140532459,"alleles":["A","G"],"strand":1,"feature_type":"variation","id":"rs1398503438","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1796304976","seq_region_name":"7","end":140532461,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140532461,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532463,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140532463,"clinical_significance":[],"id":"rs961459589","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs112413330","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140532467,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532467},{"id":"rs1022591147","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140532469,"strand":1,"feature_type":"variation","start":140532469,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs888204304","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532473,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140532473},{"alleles":["G","A"],"end":140532474,"strand":1,"feature_type":"variation","start":140532474,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1244609600","clinical_significance":[]},{"clinical_significance":[],"id":"rs2130484733","seq_region_name":"7","end":140532480,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140532480,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532481,"source":"dbSNP","strand":1,"feature_type":"variation","end":140532481,"alleles":["A","G","T"],"seq_region_name":"7","id":"rs1005250326","clinical_significance":[]},{"id":"rs1796305676","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532482,"source":"dbSNP","strand":1,"feature_type":"variation","end":140532482,"alleles":["T","C"]},{"id":"rs1585564824","seq_region_name":"7","clinical_significance":[],"start":140532483,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140532483,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"id":"rs1015421286","seq_region_name":"7","clinical_significance":[],"end":140532484,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140532484,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["C","T"],"end":140532485,"feature_type":"variation","strand":1,"source":"dbSNP","start":140532485,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1563121336"},{"alleles":["C","T"],"end":140532491,"strand":1,"feature_type":"variation","start":140532491,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs530444602","clinical_significance":[]},{"start":140532492,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140532492,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs976723182","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532493,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140532493,"clinical_significance":[],"seq_region_name":"7","id":"rs1373117145"},{"end":140532494,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140532494,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs936243995"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1211504291","feature_type":"variation","strand":1,"end":140532495,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532495},{"source":"dbSNP","start":140532500,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140532500,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1796306489","seq_region_name":"7"},{"end":140532501,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140532501,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs73485794"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140532503,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532503,"source":"dbSNP","seq_region_name":"7","id":"rs2130484851","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140532506,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532506,"clinical_significance":[],"seq_region_name":"7","id":"rs1796306695"},{"end":140532507,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140532507,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796306772","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140532512,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532512,"clinical_significance":[],"seq_region_name":"7","id":"rs570764559"},{"source":"dbSNP","start":140532518,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140532518,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1218675214"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532522,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140532522,"seq_region_name":"7","id":"rs1340365977","clinical_significance":[]},{"seq_region_name":"7","id":"rs1272117959","clinical_significance":[],"strand":1,"feature_type":"variation","end":140532528,"alleles":["CACA","CA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532525,"source":"dbSNP"},{"source":"dbSNP","start":140532526,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140532526,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs2130484905","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1796307233","clinical_significance":[],"start":140532527,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140532527,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs561034457","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532533,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140532533},{"end":140532538,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140532538,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796307315"},{"alleles":["C","G"],"end":140532541,"feature_type":"variation","strand":1,"source":"dbSNP","start":140532541,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796307398"},{"feature_type":"variation","strand":1,"end":140532545,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532545,"clinical_significance":[],"seq_region_name":"7","id":"rs1399360448"},{"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140532555,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532555,"clinical_significance":[],"seq_region_name":"7","id":"rs1046131873"},{"source":"dbSNP","start":140532562,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140532562,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs986547349"},{"seq_region_name":"7","id":"rs910549444","clinical_significance":[],"strand":1,"feature_type":"variation","end":140532564,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532564,"source":"dbSNP"},{"source":"dbSNP","start":140532572,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140532573,"alleles":["TT","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130484988"},{"source":"dbSNP","start":140532573,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140532573,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796307748"},{"source":"dbSNP","start":140532575,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140532575,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796307820"},{"clinical_significance":[],"id":"rs1001981382","seq_region_name":"7","source":"dbSNP","start":140532576,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C","T"],"end":140532576,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140532585,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140532585,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796308027"},{"seq_region_name":"7","id":"rs1054941801","clinical_significance":[],"alleles":["G","A"],"end":140532590,"strand":1,"feature_type":"variation","start":140532590,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140532602,"alleles":["T","TT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532602,"clinical_significance":[],"seq_region_name":"7","id":"rs1357882335"},{"feature_type":"variation","strand":1,"end":140532603,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532603,"clinical_significance":[],"seq_region_name":"7","id":"rs1331663623"},{"seq_region_name":"7","id":"rs1413376419","clinical_significance":[],"start":140532604,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C","T"],"end":140532604,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532604,"feature_type":"variation","strand":1,"alleles":["GG","G"],"end":140532605,"clinical_significance":[],"id":"rs1796308535","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1419850557","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532605,"feature_type":"variation","strand":1,"end":140532605,"alleles":["G","C"]},{"seq_region_name":"7","id":"rs1585565027","clinical_significance":[],"strand":1,"feature_type":"variation","end":140532611,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532611,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1796308788","clinical_significance":[],"start":140532613,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C","G"],"end":140532613,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140532614,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140532614,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1172357986"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532615,"feature_type":"variation","strand":1,"end":140532615,"alleles":["G","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs141638319"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532618,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140532618,"clinical_significance":[],"seq_region_name":"7","id":"rs1796308954"},{"alleles":["A","G"],"end":140532623,"strand":1,"feature_type":"variation","start":140532623,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1338395287","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140532631,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532631,"source":"dbSNP","seq_region_name":"7","id":"rs1796309123","clinical_significance":[]},{"end":140532632,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140532632,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs191629812","seq_region_name":"7"},{"id":"rs1404652545","seq_region_name":"7","clinical_significance":[],"start":140532635,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["CTCT","CT"],"end":140532638,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs978825336","feature_type":"variation","strand":1,"end":140532638,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532638},{"seq_region_name":"7","id":"rs1796309487","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140532639,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532639,"source":"dbSNP"},{"source":"dbSNP","start":140532642,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140532642,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1333638576","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1005431350","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140532645,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532645,"source":"dbSNP"},{"clinical_significance":[],"id":"rs924802416","seq_region_name":"7","alleles":["G","T"],"end":140532646,"feature_type":"variation","strand":1,"source":"dbSNP","start":140532646,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1796309858","seq_region_name":"7","alleles":["T","C"],"end":140532649,"feature_type":"variation","strand":1,"source":"dbSNP","start":140532649,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1209562677","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532650,"source":"dbSNP","strand":1,"feature_type":"variation","end":140532653,"alleles":["GGGG","GGGGG"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1438448836","source":"dbSNP","start":140532651,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140532651,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140532652,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532652,"clinical_significance":[],"id":"rs1275459707","seq_region_name":"7"},{"end":140532656,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140532656,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs147075025","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1796310319","seq_region_name":"7","source":"dbSNP","start":140532662,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140532662,"feature_type":"variation","strand":1},{"end":140532665,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140532665,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1217034854"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532667,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140532667,"seq_region_name":"7","id":"rs1796310491","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140532669,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532669,"source":"dbSNP","seq_region_name":"7","id":"rs1317459615","clinical_significance":[]},{"start":140532670,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140532670,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs2130485239","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs934838139","feature_type":"variation","strand":1,"end":140532687,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532687},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796310749","feature_type":"variation","strand":1,"end":140532690,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532690},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532695,"source":"dbSNP","strand":1,"feature_type":"variation","end":140532695,"alleles":["G","C"],"id":"rs1796310845","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796310933","clinical_significance":[],"alleles":["G","T"],"end":140532699,"strand":1,"feature_type":"variation","start":140532699,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532701,"source":"dbSNP","strand":1,"feature_type":"variation","end":140532701,"alleles":["T","C"],"id":"rs1294312732","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","A"],"end":140532702,"feature_type":"variation","strand":1,"source":"dbSNP","start":140532702,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1796311093","seq_region_name":"7"},{"source":"dbSNP","start":140532705,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140532705,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs961365891","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1796311286","clinical_significance":[],"end":140532711,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140532711,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140532714,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140532714,"alleles":["G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796311362","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1057277965","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140532717,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532717},{"clinical_significance":[],"seq_region_name":"7","id":"rs1284102294","feature_type":"variation","strand":1,"end":140532718,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532718},{"feature_type":"variation","strand":1,"end":140532730,"alleles":["AGGCA","AGGCAGGCA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532726,"clinical_significance":[],"seq_region_name":"7","id":"rs1796311601"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532729,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140532729,"id":"rs1029738049","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1317783365","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532731,"feature_type":"variation","strand":1,"end":140532731,"alleles":["C","A"]},{"seq_region_name":"7","id":"rs896060432","clinical_significance":[],"strand":1,"feature_type":"variation","end":140532735,"alleles":["A","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532735,"source":"dbSNP"},{"seq_region_name":"7","id":"rs138461450","clinical_significance":[],"alleles":["C","A","T"],"end":140532736,"strand":1,"feature_type":"variation","start":140532736,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140532737,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140532737,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1332718866","clinical_significance":[]},{"end":140532747,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140532747,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796312197","clinical_significance":[]},{"seq_region_name":"7","id":"rs1044487572","clinical_significance":[],"strand":1,"feature_type":"variation","end":140532750,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532750,"source":"dbSNP"},{"source":"dbSNP","start":140532751,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140532751,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796312377"},{"seq_region_name":"7","id":"rs775957113","clinical_significance":[],"start":140532753,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140532753,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1796312547","clinical_significance":[],"start":140532758,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140532758,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532761,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140532761,"seq_region_name":"7","id":"rs550686834","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796312743","alleles":["A","G"],"end":140532764,"feature_type":"variation","strand":1,"source":"dbSNP","start":140532764,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140532767,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532767,"source":"dbSNP","seq_region_name":"7","id":"rs888110815","clinical_significance":[]},{"source":"dbSNP","start":140532769,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140532769,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs183635923"},{"id":"rs1796313012","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532770,"source":"dbSNP","strand":1,"feature_type":"variation","end":140532770,"alleles":["A","C"]},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140532774,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532774,"source":"dbSNP","id":"rs1005281659","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1411605561","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532781,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140532781},{"seq_region_name":"7","id":"rs1181200956","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140532783,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532783,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1796313371","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532787,"feature_type":"variation","strand":1,"end":140532787,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1796313487","clinical_significance":[],"start":140532791,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140532791,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1036725204","clinical_significance":[],"strand":1,"feature_type":"variation","end":140532794,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532794,"source":"dbSNP"},{"start":140532800,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140532800,"strand":1,"feature_type":"variation","id":"rs1796313658","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140532800,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["GG","G"],"end":140532801,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs772178358"},{"seq_region_name":"7","id":"rs1796313828","clinical_significance":[],"end":140532803,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140532803,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs870217","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140532811,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532811},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532811,"feature_type":"variation","strand":1,"end":140532813,"alleles":["TCT","GCC"],"clinical_significance":[],"seq_region_name":"7","id":"rs386718479"},{"end":140532812,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140532812,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1796314125","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140532813,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532813,"source":"dbSNP","seq_region_name":"7","id":"rs870216","clinical_significance":[]},{"end":140532817,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140532817,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1796314376","seq_region_name":"7"},{"seq_region_name":"7","id":"rs745731989","clinical_significance":[],"strand":1,"feature_type":"variation","end":140532819,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532819,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1196769742","seq_region_name":"7","source":"dbSNP","start":140532823,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140532823,"feature_type":"variation","strand":1},{"id":"rs1796314627","seq_region_name":"7","clinical_significance":[],"end":140532827,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140532827,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532830,"feature_type":"variation","strand":1,"end":140532830,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130485614"},{"feature_type":"variation","strand":1,"end":140532837,"alleles":["C","A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532837,"clinical_significance":[],"seq_region_name":"7","id":"rs1457507093"},{"id":"rs1274008090","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140532839,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532839,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140532840,"alleles":["C","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532840,"source":"dbSNP","seq_region_name":"7","id":"rs1215995948","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796315036","clinical_significance":[],"strand":1,"feature_type":"variation","end":140532841,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532841,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs187734189","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140532842,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532842},{"seq_region_name":"7","id":"rs954134921","clinical_significance":[],"start":140532850,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140532850,"alleles":["T","G"],"strand":1,"feature_type":"variation"},{"id":"rs945027408","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532856,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140532856},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796315450","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532857,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140532857},{"seq_region_name":"7","id":"rs1796315528","clinical_significance":[],"alleles":["C","T"],"end":140532865,"strand":1,"feature_type":"variation","start":140532865,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140532866,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AAAAAA","AAAAA"],"end":140532871,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1376096390"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1006806489","source":"dbSNP","start":140532876,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140532876,"alleles":["A","C"],"feature_type":"variation","strand":1},{"end":140532877,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140532877,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1017643935","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140532879,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532879,"clinical_significance":[],"seq_region_name":"7","id":"rs1375750233"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1680298979","source":"dbSNP","start":140532881,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140532881,"alleles":["T","C"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532883,"source":"dbSNP","strand":1,"feature_type":"variation","end":140532883,"alleles":["T","C"],"seq_region_name":"7","id":"rs927732724","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532884,"feature_type":"variation","strand":1,"end":140532884,"alleles":["A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs534546337"},{"strand":1,"feature_type":"variation","end":140532888,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532888,"source":"dbSNP","id":"rs868385032","seq_region_name":"7","clinical_significance":[]},{"end":140532893,"alleles":["AGGAGG","AGGAGGCACAGGAGG"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140532888,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs200880876"},{"end":140532889,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140532889,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs866962184"},{"id":"rs2130485778","seq_region_name":"7","clinical_significance":[],"end":140532889,"alleles":["-","T"],"strand":1,"feature_type":"variation","start":140532890,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532890,"feature_type":"variation","strand":1,"end":140532890,"alleles":["G","T"],"clinical_significance":[],"id":"rs1585565540","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140532893,"alleles":["GAGG","GAGGCACACTGAGG","GAGGCACAGCGAGG","GAGGCACAGTGAGG"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532890,"source":"dbSNP","seq_region_name":"7","id":"rs5887979","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796316417","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532895,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140532895},{"alleles":["C","T"],"end":140532899,"strand":1,"feature_type":"variation","start":140532899,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1382051490","seq_region_name":"7","clinical_significance":[]},{"start":140532907,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140532907,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","id":"rs559286241","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796316694","end":140532908,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140532908,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["TTTTTTTT","TTTTTTT","TTTTTTTTT"],"end":140532915,"feature_type":"variation","strand":1,"source":"dbSNP","start":140532908,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs937735135"},{"end":140532908,"alleles":["-","G"],"strand":1,"feature_type":"variation","start":140532909,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1563121563","clinical_significance":[]},{"start":140532909,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140532909,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1375690951","clinical_significance":[]},{"seq_region_name":"7","id":"rs1193134789","clinical_significance":[],"end":140532912,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140532912,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140532913,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532913,"source":"dbSNP","seq_region_name":"7","id":"rs1796317365","clinical_significance":[]},{"seq_region_name":"7","id":"rs577547225","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532915,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140532915},{"clinical_significance":[],"seq_region_name":"7","id":"rs762143665","source":"dbSNP","start":140532916,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140532916,"feature_type":"variation","strand":1},{"id":"rs1265244513","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532917,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140532917},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140532918,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532918,"clinical_significance":[],"seq_region_name":"7","id":"rs1796317751"},{"alleles":["T","C"],"end":140532924,"strand":1,"feature_type":"variation","start":140532924,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796317845","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1322473336","end":140532930,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140532930,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs2130485952","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532932,"source":"dbSNP","strand":1,"feature_type":"variation","end":140532932,"alleles":["G","C"]},{"seq_region_name":"7","id":"rs888276692","clinical_significance":[],"end":140532933,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140532933,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140532938,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532938,"clinical_significance":[],"seq_region_name":"7","id":"rs2130485977"},{"start":140532944,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AAAAA","AAAAAA"],"end":140532948,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796318142","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796318220","clinical_significance":[],"start":140532948,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140532948,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140532952,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532952,"clinical_significance":[],"seq_region_name":"7","id":"rs2130486010"},{"end":140532953,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140532953,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796318314"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796318420","end":140532961,"alleles":["TTTAACTTT","TTT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140532953,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140532957,"alleles":["A","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532957,"clinical_significance":[],"seq_region_name":"7","id":"rs924708823"},{"end":140532965,"alleles":["TTTTTTT","TTTTTTTT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140532959,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1563121577"},{"seq_region_name":"7","id":"rs1302472269","clinical_significance":[],"start":140532964,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140532964,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130486074","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532972,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140532972},{"end":140532973,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140532973,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1237391919"},{"id":"rs1385857122","seq_region_name":"7","clinical_significance":[],"start":140532974,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140532980,"alleles":["AAAGAAA","AAA"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140532977,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532977,"source":"dbSNP","seq_region_name":"7","id":"rs377529440","clinical_significance":[]},{"seq_region_name":"7","id":"rs1331368686","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140532983,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532983,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532984,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CTACCT","CT"],"end":140532989,"seq_region_name":"7","id":"rs1364988480","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532987,"feature_type":"variation","strand":1,"end":140532987,"alleles":["C","T"],"clinical_significance":[],"id":"rs1005919266","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796319409","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140532988,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532988},{"feature_type":"variation","strand":1,"alleles":["T","TT"],"end":140532989,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532989,"clinical_significance":[],"seq_region_name":"7","id":"rs1796319496"},{"feature_type":"variation","strand":1,"end":140532990,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532990,"clinical_significance":[],"id":"rs993413865","seq_region_name":"7"},{"source":"dbSNP","start":140532991,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["-","TTT"],"end":140532990,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796319684"},{"id":"rs917415377","seq_region_name":"7","clinical_significance":[],"start":140532991,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140532991,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1036932053","end":140532991,"alleles":["C","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140532991,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1489464964","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140532992,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532992,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs3042406","alleles":["TTTTTTTTTTTTTTTTTTT","TTTTTTT","TTTTTTTTTTT","TTTTTTTTTTTT","TTTTTTTTTTTTT","TTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT"],"end":140533010,"feature_type":"variation","strand":1,"source":"dbSNP","start":140532992,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140532993,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140532993,"source":"dbSNP","seq_region_name":"7","id":"rs897188973","clinical_significance":[]},{"alleles":["T","TCT"],"end":140532994,"strand":1,"feature_type":"variation","start":140532994,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796320708","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1216522166","feature_type":"variation","strand":1,"end":140532995,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140532995},{"start":140533001,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140533000,"alleles":["-","G"],"strand":1,"feature_type":"variation","id":"rs1796320804","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1486250115","seq_region_name":"7","source":"dbSNP","start":140533009,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140533009,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1796320990","clinical_significance":[],"alleles":["TG","-"],"end":140533011,"strand":1,"feature_type":"variation","start":140533010,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533011,"feature_type":"variation","strand":1,"end":140533010,"alleles":["-","TTTA"],"clinical_significance":[],"seq_region_name":"7","id":"rs1796321092"},{"seq_region_name":"7","id":"rs1280445368","clinical_significance":[],"strand":1,"feature_type":"variation","end":140533011,"alleles":["G","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533011,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140533011,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533011,"source":"dbSNP","seq_region_name":"7","id":"rs1421382126","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533012,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G","T"],"end":140533012,"seq_region_name":"7","id":"rs1162075899","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796321500","clinical_significance":[],"alleles":["A","-"],"end":140533012,"strand":1,"feature_type":"variation","start":140533012,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1295069985","feature_type":"variation","strand":1,"end":140533012,"alleles":["-","TTTT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533013},{"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140533013,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533013,"clinical_significance":[],"seq_region_name":"7","id":"rs1340483107"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1300138527","feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140533014,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533014},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130486381","feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140533015,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533015},{"clinical_significance":[],"id":"rs544799838","seq_region_name":"7","end":140533016,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140533016,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140533017,"alleles":["AG","GA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533016,"source":"dbSNP","id":"rs386718480","seq_region_name":"7","clinical_significance":[]},{"end":140533017,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140533017,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs556794278","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796322213","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140533018,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533018,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1399150678","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533020,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140533020},{"seq_region_name":"7","id":"rs1585565913","clinical_significance":[],"end":140533024,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140533024,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796322445","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533028,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140533028},{"start":140533032,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140533032,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796322526","clinical_significance":[]},{"start":140533033,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["CC","CCC"],"end":140533034,"strand":1,"feature_type":"variation","id":"rs1796322633","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","T"],"end":140533034,"feature_type":"variation","strand":1,"source":"dbSNP","start":140533034,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1375888634"},{"seq_region_name":"7","id":"rs1585565929","clinical_significance":[],"alleles":["A","C"],"end":140533035,"strand":1,"feature_type":"variation","start":140533035,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140533038,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533038,"source":"dbSNP","seq_region_name":"7","id":"rs1796322893","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140533041,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533041,"source":"dbSNP","seq_region_name":"7","id":"rs949025922","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533042,"source":"dbSNP","strand":1,"feature_type":"variation","end":140533042,"alleles":["A","G"],"seq_region_name":"7","id":"rs1585565952","clinical_significance":[]},{"end":140533043,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140533043,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1796323199","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140533044,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533044,"clinical_significance":[],"seq_region_name":"7","id":"rs1585565957"},{"clinical_significance":[],"id":"rs1796323402","seq_region_name":"7","alleles":["G","A"],"end":140533045,"feature_type":"variation","strand":1,"source":"dbSNP","start":140533045,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140533046,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140533046,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1232159260"},{"end":140533047,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140533047,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2001673","clinical_significance":[]},{"alleles":["T","G"],"end":140533049,"strand":1,"feature_type":"variation","start":140533049,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796323660","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533051,"source":"dbSNP","strand":1,"feature_type":"variation","end":140533051,"alleles":["G","A"],"seq_region_name":"7","id":"rs1796323764","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533054,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140533054,"seq_region_name":"7","id":"rs909580122","clinical_significance":[]},{"alleles":["G","A"],"end":140533055,"feature_type":"variation","strand":1,"source":"dbSNP","start":140533055,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs941041699"},{"seq_region_name":"7","id":"rs1796324087","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140533063,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533063,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1213859233","clinical_significance":[],"start":140533064,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140533064,"strand":1,"feature_type":"variation"},{"end":140533065,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140533065,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1796324285","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533066,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140533066,"clinical_significance":[],"seq_region_name":"7","id":"rs542260057"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533067,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140533067,"clinical_significance":[],"id":"rs1193641486","seq_region_name":"7"},{"alleles":["T","C"],"end":140533068,"strand":1,"feature_type":"variation","start":140533068,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1475723595","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796324653","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533074,"source":"dbSNP","strand":1,"feature_type":"variation","end":140533074,"alleles":["C","T"]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140533076,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533076,"source":"dbSNP","seq_region_name":"7","id":"rs954113768","clinical_significance":[]},{"source":"dbSNP","start":140533083,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140533083,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1006943647"},{"seq_region_name":"7","id":"rs1254838350","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533084,"source":"dbSNP","strand":1,"feature_type":"variation","end":140533084,"alleles":["C","A","T"]},{"strand":1,"feature_type":"variation","end":140533087,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533087,"source":"dbSNP","seq_region_name":"7","id":"rs1319457083","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796325041","clinical_significance":[],"alleles":["TTCTTCT","TTCT"],"end":140533103,"strand":1,"feature_type":"variation","start":140533097,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1796325145","seq_region_name":"7","clinical_significance":[],"start":140533098,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140533098,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1796325235","seq_region_name":"7","feature_type":"variation","strand":1,"end":140533099,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533099},{"clinical_significance":[],"id":"rs1276199642","seq_region_name":"7","alleles":["C","T"],"end":140533112,"feature_type":"variation","strand":1,"source":"dbSNP","start":140533112,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs560984164","alleles":["A","G"],"end":140533118,"feature_type":"variation","strand":1,"source":"dbSNP","start":140533118,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1355806534","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533122,"feature_type":"variation","strand":1,"end":140533122,"alleles":["G","A"]},{"feature_type":"variation","strand":1,"end":140533123,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533123,"clinical_significance":[],"seq_region_name":"7","id":"rs957559107"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585566132","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533124,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140533124},{"clinical_significance":[],"id":"rs1796325880","seq_region_name":"7","feature_type":"variation","strand":1,"end":140533127,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533127},{"clinical_significance":[],"seq_region_name":"7","id":"rs1314635998","feature_type":"variation","strand":1,"end":140533137,"alleles":["GACTACAGGTG","GACTACAGGTGACTACAGGTG"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533127},{"clinical_significance":[],"id":"rs1796326081","seq_region_name":"7","end":140533128,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140533128,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","T"],"end":140533132,"feature_type":"variation","strand":1,"source":"dbSNP","start":140533132,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs896898872","seq_region_name":"7"},{"end":140533134,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140533134,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796326276"},{"start":140533136,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140533136,"strand":1,"feature_type":"variation","id":"rs532724509","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533139,"source":"dbSNP","strand":1,"feature_type":"variation","end":140533139,"alleles":["G","T"],"seq_region_name":"7","id":"rs1228976146","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533140,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140533140,"id":"rs1201474133","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796326677","feature_type":"variation","strand":1,"end":140533141,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533141},{"clinical_significance":[],"seq_region_name":"7","id":"rs528064520","end":140533145,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140533145,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796326884","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533148,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140533148},{"alleles":["C","T"],"end":140533150,"feature_type":"variation","strand":1,"source":"dbSNP","start":140533150,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796326985"},{"id":"rs1563121723","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140533151,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533151,"source":"dbSNP"},{"id":"rs1796327188","seq_region_name":"7","clinical_significance":[],"start":140533154,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140533154,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533155,"feature_type":"variation","strand":1,"end":140533155,"alleles":["C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1394449348"},{"alleles":["A","G"],"end":140533158,"feature_type":"variation","strand":1,"source":"dbSNP","start":140533158,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796327382"},{"start":140533159,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140533159,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1401768773","clinical_significance":[]},{"alleles":["TTTTTT","TTTTTTT"],"end":140533164,"strand":1,"feature_type":"variation","start":140533159,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1265078256","seq_region_name":"7","clinical_significance":[]},{"start":140533160,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140533160,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796327638","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796327715","clinical_significance":[],"alleles":["T","G"],"end":140533163,"strand":1,"feature_type":"variation","start":140533163,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140533165,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533165,"clinical_significance":[],"seq_region_name":"7","id":"rs1585566226"},{"source":"dbSNP","start":140533166,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140533166,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796327945"},{"id":"rs1796328018","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140533173,"alleles":["G","A","C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533173,"source":"dbSNP"},{"start":140533174,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140533174,"alleles":["G","T"],"strand":1,"feature_type":"variation","id":"rs1796328168","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533177,"source":"dbSNP","strand":1,"feature_type":"variation","end":140533177,"alleles":["G","A"],"seq_region_name":"7","id":"rs1432383297","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796328367","source":"dbSNP","start":140533179,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140533179,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533181,"source":"dbSNP","strand":1,"feature_type":"variation","end":140533181,"alleles":["C","T"],"id":"rs997939346","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533182,"feature_type":"variation","strand":1,"end":140533182,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585566257"},{"feature_type":"variation","strand":1,"end":140533184,"alleles":["G","C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533184,"clinical_significance":[],"seq_region_name":"7","id":"rs1796328687"},{"end":140533190,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140533190,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796328792"},{"clinical_significance":[],"id":"rs1051409937","seq_region_name":"7","source":"dbSNP","start":140533194,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140533194,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533199,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140533199,"seq_region_name":"7","id":"rs1467231854","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140533201,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533201,"source":"dbSNP","seq_region_name":"7","id":"rs1796329200","clinical_significance":[]},{"alleles":["A","G"],"end":140533202,"feature_type":"variation","strand":1,"source":"dbSNP","start":140533202,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs889612097"},{"strand":1,"feature_type":"variation","end":140533206,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533206,"source":"dbSNP","id":"rs2130487003","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796329513","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140533207,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533207},{"feature_type":"variation","strand":1,"end":140533208,"alleles":["GG","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533207,"clinical_significance":[],"seq_region_name":"7","id":"rs1796329658"},{"source":"dbSNP","start":140533212,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140533212,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs540167740"},{"seq_region_name":"7","id":"rs564814689","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533213,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140533213},{"alleles":["T","A","C"],"end":140533215,"feature_type":"variation","strand":1,"source":"dbSNP","start":140533215,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1370506575"},{"feature_type":"variation","strand":1,"end":140533216,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533216,"clinical_significance":[],"id":"rs1796330357","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1796330438","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533220,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TGACCTCATGATCC","-"],"end":140533233},{"clinical_significance":[],"seq_region_name":"7","id":"rs150249526","source":"dbSNP","start":140533224,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140533224,"alleles":["C","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796330641","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533226,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140533226},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796330749","alleles":["A","G"],"end":140533227,"feature_type":"variation","strand":1,"source":"dbSNP","start":140533227,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1000201307","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533231,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140533231},{"start":140533235,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140533235,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796330935","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796331027","clinical_significance":[],"alleles":["C","A"],"end":140533236,"strand":1,"feature_type":"variation","start":140533236,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533237,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140533237,"clinical_significance":[],"seq_region_name":"7","id":"rs192650914"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1156972433","feature_type":"variation","strand":1,"end":140533238,"alleles":["G","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533238},{"seq_region_name":"7","id":"rs1796331514","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533239,"source":"dbSNP","strand":1,"feature_type":"variation","end":140533239,"alleles":["A","C"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533240,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140533240,"clinical_significance":[],"seq_region_name":"7","id":"rs2130487151"},{"seq_region_name":"7","id":"rs1796331599","clinical_significance":[],"alleles":["A","G"],"end":140533243,"strand":1,"feature_type":"variation","start":140533243,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533244,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C","T"],"end":140533244,"id":"rs35683312","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1796331702","seq_region_name":"7","feature_type":"variation","strand":1,"end":140533246,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533246},{"seq_region_name":"7","id":"rs1563121785","clinical_significance":[],"start":140533247,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140533247,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796331920","alleles":["C","A"],"end":140533248,"feature_type":"variation","strand":1,"source":"dbSNP","start":140533248,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["A","G"],"end":140533252,"strand":1,"feature_type":"variation","start":140533252,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1197876445","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796332125","source":"dbSNP","start":140533253,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140533268,"alleles":["AGTGCTGGGATTACAG","AG"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs992922171","clinical_significance":[],"start":140533254,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140533254,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs927596842","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533257,"source":"dbSNP","strand":1,"feature_type":"variation","end":140533257,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1242329476","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533262,"feature_type":"variation","strand":1,"end":140533262,"alleles":["A","T"]},{"clinical_significance":[],"id":"rs1339711199","seq_region_name":"7","alleles":["C","T"],"end":140533266,"feature_type":"variation","strand":1,"source":"dbSNP","start":140533266,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1295795760","seq_region_name":"7","source":"dbSNP","start":140533269,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140533269,"alleles":["G","A"],"feature_type":"variation","strand":1},{"end":140533270,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140533270,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1366021838","clinical_significance":[]},{"seq_region_name":"7","id":"rs937791263","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140533271,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533271,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796333185","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533273,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140533273},{"seq_region_name":"7","id":"rs1449324943","clinical_significance":[],"start":140533276,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140533276,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs759639467","clinical_significance":[],"end":140533279,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140533279,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533280,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140533280,"clinical_significance":[],"seq_region_name":"7","id":"rs1796333547"},{"strand":1,"feature_type":"variation","alleles":["GC","-"],"end":140533282,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533281,"source":"dbSNP","seq_region_name":"7","id":"rs1796333656","clinical_significance":[]},{"clinical_significance":[],"id":"rs1796333748","seq_region_name":"7","source":"dbSNP","start":140533284,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140533283,"alleles":["-","TC"],"feature_type":"variation","strand":1},{"alleles":["C","A","T"],"end":140533284,"strand":1,"feature_type":"variation","start":140533284,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1374700773","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533288,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140533288,"seq_region_name":"7","id":"rs1330782215","clinical_significance":[]},{"seq_region_name":"7","id":"rs1462364373","clinical_significance":[],"alleles":["C","T"],"end":140533297,"strand":1,"feature_type":"variation","start":140533297,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1796334159","clinical_significance":[],"alleles":["TTTTT","TTTTTT"],"end":140533306,"strand":1,"feature_type":"variation","start":140533302,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs990581483","clinical_significance":[],"strand":1,"feature_type":"variation","end":140533304,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533304,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796334352","source":"dbSNP","start":140533317,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140533317,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533319,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140533319,"seq_region_name":"7","id":"rs1796334462","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585566493","clinical_significance":[],"alleles":["C","G"],"end":140533320,"strand":1,"feature_type":"variation","start":140533320,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140533321,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533321,"clinical_significance":[],"seq_region_name":"7","id":"rs1563121833"},{"clinical_significance":[],"id":"rs917429454","seq_region_name":"7","source":"dbSNP","start":140533322,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140533322,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1796334819","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533324,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140533324},{"source":"dbSNP","start":140533334,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140533334,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796334909"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796334999","source":"dbSNP","start":140533337,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140533337,"alleles":["G","A","T"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533339,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140533339,"seq_region_name":"7","id":"rs534676937","clinical_significance":[]},{"start":140533340,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140533340,"strand":1,"feature_type":"variation","id":"rs1162036564","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796335296","clinical_significance":[],"alleles":["T","A","C"],"end":140533341,"strand":1,"feature_type":"variation","start":140533341,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1796335438","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533344,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140533344},{"alleles":["G","A","C"],"end":140533347,"strand":1,"feature_type":"variation","start":140533347,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1585566554","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs980209250","clinical_significance":[],"end":140533349,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140533349,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["C","T"],"end":140533356,"strand":1,"feature_type":"variation","start":140533356,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796335763","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs909730084","end":140533357,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140533357,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1364778335","source":"dbSNP","start":140533359,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TCTCCTTGCTGTACAGCCCCTTGGG","-"],"end":140533383,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1235764022","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533360,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140533360},{"strand":1,"feature_type":"variation","end":140533364,"alleles":["CTCCT","CT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533360,"source":"dbSNP","id":"rs1158833768","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs990972485","end":140533402,"alleles":["CTCCTTGCTGTACAGCCCCTTGGGGCTCCTTGCTGTACAGCCC","CTCCTTGCTGTACAGCCC"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140533360,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1177466802","seq_region_name":"7","clinical_significance":[],"alleles":["C","A","T"],"end":140533362,"strand":1,"feature_type":"variation","start":140533362,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1796336509","clinical_significance":[],"alleles":["G","T"],"end":140533366,"strand":1,"feature_type":"variation","start":140533366,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["T","C"],"end":140533368,"feature_type":"variation","strand":1,"source":"dbSNP","start":140533368,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796336605"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533379,"feature_type":"variation","strand":1,"end":140533379,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1237471950"},{"strand":1,"feature_type":"variation","alleles":["TT","T"],"end":140533380,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533379,"source":"dbSNP","seq_region_name":"7","id":"rs1378701813","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1036837487","source":"dbSNP","start":140533382,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140533382,"alleles":["G","C"],"feature_type":"variation","strand":1},{"id":"rs1796336918","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533383,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GGCTCCTTGCTGTACAGCCCTTTGTG","G"],"end":140533408},{"source":"dbSNP","start":140533385,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","G"],"end":140533385,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796337031"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533387,"source":"dbSNP","strand":1,"feature_type":"variation","end":140533387,"alleles":["C","T"],"seq_region_name":"7","id":"rs910150677","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796337269","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533388,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140533388},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140533391,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533391,"clinical_significance":[],"seq_region_name":"7","id":"rs1796337377"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533393,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140533393,"id":"rs2130487639","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","T"],"end":140533397,"feature_type":"variation","strand":1,"source":"dbSNP","start":140533397,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs933857438","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796337586","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140533398,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533398},{"start":140533399,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140533399,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796337701","clinical_significance":[]},{"alleles":["C","G"],"end":140533402,"strand":1,"feature_type":"variation","start":140533402,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796337802","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796337968","source":"dbSNP","start":140533403,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140533403,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1796338120","clinical_significance":[],"start":140533406,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140533406,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140533407,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140533407,"alleles":["T","A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs7806065","seq_region_name":"7"},{"alleles":["T","G"],"end":140533411,"strand":1,"feature_type":"variation","start":140533411,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs752658946","clinical_significance":[]},{"seq_region_name":"7","id":"rs1007426592","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533413,"source":"dbSNP","strand":1,"feature_type":"variation","end":140533413,"alleles":["C","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533420,"source":"dbSNP","strand":1,"feature_type":"variation","end":140533420,"alleles":["C","T"],"seq_region_name":"7","id":"rs1796338891","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533421,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140533421,"id":"rs1585566724","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533423,"feature_type":"variation","strand":1,"end":140533423,"alleles":["A","G"],"clinical_significance":[],"id":"rs972378384","seq_region_name":"7"},{"source":"dbSNP","start":140533424,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A","C"],"end":140533424,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796339363"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533425,"source":"dbSNP","strand":1,"feature_type":"variation","end":140533425,"alleles":["G","A"],"seq_region_name":"7","id":"rs1796339502","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796339632","clinical_significance":[],"start":140533426,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140533426,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140533430,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140533430,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs548390484","seq_region_name":"7"},{"id":"rs1796340004","seq_region_name":"7","clinical_significance":[],"end":140533433,"alleles":["CTTC","C"],"strand":1,"feature_type":"variation","start":140533430,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533431,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140533431,"seq_region_name":"7","id":"rs933761158","clinical_significance":[]},{"seq_region_name":"7","id":"rs1322109309","clinical_significance":[],"start":140533435,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140533435,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533437,"source":"dbSNP","strand":1,"feature_type":"variation","end":140533437,"alleles":["G","A"],"seq_region_name":"7","id":"rs1796340433","clinical_significance":[]},{"source":"dbSNP","start":140533440,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140533440,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796340577"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1020388039","source":"dbSNP","start":140533445,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140533445,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796340847","source":"dbSNP","start":140533446,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140533446,"alleles":["G","A"],"feature_type":"variation","strand":1},{"start":140533447,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140533447,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1263624675","clinical_significance":[]},{"end":140533451,"alleles":["CCCCC","CCCCCC"],"strand":1,"feature_type":"variation","start":140533447,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1386065797","clinical_significance":[]},{"clinical_significance":[],"id":"rs971627322","seq_region_name":"7","feature_type":"variation","strand":1,"end":140533448,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533448},{"clinical_significance":[],"seq_region_name":"7","id":"rs1421066721","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533449,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140533449},{"seq_region_name":"7","id":"rs1378089648","clinical_significance":[],"alleles":["C","G"],"end":140533450,"strand":1,"feature_type":"variation","start":140533450,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1488088054","source":"dbSNP","start":140533452,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","AA"],"end":140533452,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1478054089","source":"dbSNP","start":140533455,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140533455,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1177601421","clinical_significance":[],"start":140533458,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140533458,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"id":"rs1196605748","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533463,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140533463},{"id":"rs1050855153","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140533465,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533465,"source":"dbSNP"},{"source":"dbSNP","start":140533467,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140533467,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs566912296"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533468,"source":"dbSNP","strand":1,"feature_type":"variation","end":140533468,"alleles":["G","A"],"seq_region_name":"7","id":"rs1441824701","clinical_significance":[]},{"alleles":["G","A"],"end":140533469,"feature_type":"variation","strand":1,"source":"dbSNP","start":140533469,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs534170322","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs558390937","source":"dbSNP","start":140533471,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140533471,"feature_type":"variation","strand":1},{"id":"rs1796343184","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140533474,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533474,"source":"dbSNP"},{"end":140533475,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140533475,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs79098738"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533477,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140533477,"clinical_significance":[],"seq_region_name":"7","id":"rs750417474"},{"clinical_significance":[],"id":"rs553343655","seq_region_name":"7","source":"dbSNP","start":140533480,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140533480,"alleles":["T","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs528080469","feature_type":"variation","strand":1,"alleles":["G","-"],"end":140533483,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533483},{"seq_region_name":"7","id":"rs2130487975","clinical_significance":[],"strand":1,"feature_type":"variation","end":140533483,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533483,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796343684","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140533484,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533484},{"seq_region_name":"7","id":"rs1347163617","clinical_significance":[],"end":140533486,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140533486,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140533491,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140533491,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1796343863","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140533493,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533493,"source":"dbSNP","seq_region_name":"7","id":"rs1796343937","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533498,"feature_type":"variation","strand":1,"end":140533498,"alleles":["A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1796344028"},{"seq_region_name":"7","id":"rs1796344119","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533506,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140533506},{"clinical_significance":[],"seq_region_name":"7","id":"rs1273175570","end":140533512,"alleles":["GGAGGAG","GGAG"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140533506,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140533511,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140533511,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1233087679","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533512,"feature_type":"variation","strand":1,"end":140533512,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1166935230"},{"strand":1,"feature_type":"variation","end":140533515,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533515,"source":"dbSNP","seq_region_name":"7","id":"rs1300659870","clinical_significance":[]},{"source":"dbSNP","start":140533516,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140533516,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585566962"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533518,"source":"dbSNP","strand":1,"feature_type":"variation","end":140533518,"alleles":["C","T"],"id":"rs571124504","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1043540193","end":140533519,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140533519,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130488098","source":"dbSNP","start":140533523,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140533523,"alleles":["G","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1796345285","clinical_significance":[],"end":140533535,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140533535,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["A","G"],"end":140533537,"feature_type":"variation","strand":1,"source":"dbSNP","start":140533537,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796345435"},{"source":"dbSNP","start":140533538,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140533538,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs903781604","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1414708586","clinical_significance":[],"strand":1,"feature_type":"variation","end":140533542,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533542,"source":"dbSNP"},{"source":"dbSNP","start":140533546,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140533546,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1403650978"},{"seq_region_name":"7","id":"rs1796346020","clinical_significance":[],"alleles":["C","A"],"end":140533553,"strand":1,"feature_type":"variation","start":140533553,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533554,"feature_type":"variation","strand":1,"end":140533554,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs972563574"},{"id":"rs538448995","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140533555,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533555,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1796346451","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533557,"source":"dbSNP","strand":1,"feature_type":"variation","end":140533557,"alleles":["T","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796346614","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140533559,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533559},{"clinical_significance":[],"id":"rs1477448762","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533562,"feature_type":"variation","strand":1,"end":140533565,"alleles":["GATG","G"]},{"seq_region_name":"7","id":"rs918390292","clinical_significance":[],"alleles":["A","G"],"end":140533563,"strand":1,"feature_type":"variation","start":140533563,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["T","C"],"end":140533564,"strand":1,"feature_type":"variation","start":140533564,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1195821070","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs933930531","seq_region_name":"7","end":140533572,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140533572,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1262238535","source":"dbSNP","start":140533575,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140533575,"alleles":["G","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1050292318","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533576,"feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140533576},{"id":"rs1796347618","seq_region_name":"7","clinical_significance":[],"alleles":["G","T"],"end":140533577,"strand":1,"feature_type":"variation","start":140533577,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140533579,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140533579,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585567100"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533579,"feature_type":"variation","strand":1,"alleles":["AGAAACGTGACAGAAA","AGAAA"],"end":140533594,"clinical_significance":[],"seq_region_name":"7","id":"rs1796347819"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533584,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140533584,"seq_region_name":"7","id":"rs1402882169","clinical_significance":[]},{"clinical_significance":[],"id":"rs1276507235","seq_region_name":"7","end":140533585,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140533585,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533586,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140533586,"seq_region_name":"7","id":"rs1796348153","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs758166525","alleles":["G","T"],"end":140533591,"feature_type":"variation","strand":1,"source":"dbSNP","start":140533591,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["AAAGGAAGCCAAAG","AAAG"],"end":140533605,"strand":1,"feature_type":"variation","start":140533592,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs754349692","clinical_significance":[]},{"seq_region_name":"7","id":"rs556670752","clinical_significance":[],"start":140533598,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140533598,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"alleles":["C","G","T"],"end":140533601,"strand":1,"feature_type":"variation","start":140533601,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs889809299","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796348616","alleles":["A","G"],"end":140533602,"feature_type":"variation","strand":1,"source":"dbSNP","start":140533602,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140533603,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140533603,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs891775623","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1014783108","clinical_significance":[],"strand":1,"feature_type":"variation","end":140533606,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533606,"source":"dbSNP"},{"start":140533608,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140533608,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1448220093","clinical_significance":[]},{"start":140533609,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140533609,"alleles":["A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1024406007","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs149431781","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533610,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140533610},{"clinical_significance":[],"seq_region_name":"7","id":"rs779863085","source":"dbSNP","start":140533612,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","G"],"end":140533612,"feature_type":"variation","strand":1},{"start":140533614,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140533614,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796349298","clinical_significance":[]},{"start":140533619,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140533619,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs536384520","clinical_significance":[]},{"start":140533620,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140533620,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1563122012","clinical_significance":[]},{"alleles":["A","C","G"],"end":140533627,"feature_type":"variation","strand":1,"source":"dbSNP","start":140533627,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs73485799"},{"start":140533628,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140533628,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796349691","clinical_significance":[]},{"id":"rs1796349779","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533629,"source":"dbSNP","strand":1,"feature_type":"variation","end":140533629,"alleles":["G","C"]},{"alleles":["G","A","C"],"end":140533630,"feature_type":"variation","strand":1,"source":"dbSNP","start":140533630,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs572531660","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1172682485","clinical_significance":[],"alleles":["C","A"],"end":140533633,"strand":1,"feature_type":"variation","start":140533633,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1464017328","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533636,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140533636},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796350210","end":140533639,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140533639,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["CAGTGTTC","-"],"end":140533651,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533644,"clinical_significance":[],"seq_region_name":"7","id":"rs1796350297"},{"alleles":["A","C"],"end":140533645,"feature_type":"variation","strand":1,"source":"dbSNP","start":140533645,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796350387"},{"end":140533646,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140533646,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1422580390"},{"seq_region_name":"7","id":"rs1182234895","clinical_significance":[],"strand":1,"feature_type":"variation","end":140533647,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533647,"source":"dbSNP"},{"end":140533648,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140533648,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130488489","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1473692788","source":"dbSNP","start":140533651,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140533651,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs71543377","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533653,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140533653},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533655,"source":"dbSNP","strand":1,"feature_type":"variation","end":140533655,"alleles":["C","T"],"seq_region_name":"7","id":"rs1796350912","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140533658,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533658,"clinical_significance":[],"seq_region_name":"7","id":"rs1041899768"},{"start":140533662,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140533662,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","id":"rs183567193","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1003101843","end":140533663,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140533663,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1197240716","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140533664,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533664,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140533665,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533665,"source":"dbSNP","seq_region_name":"7","id":"rs2130488567","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140533668,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533668,"clinical_significance":[],"seq_region_name":"7","id":"rs1205108619"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140533671,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533671,"source":"dbSNP","seq_region_name":"7","id":"rs1796351411","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796351505","clinical_significance":[],"start":140533672,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140533672,"strand":1,"feature_type":"variation"},{"id":"rs2130488619","seq_region_name":"7","clinical_significance":[],"end":140533673,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140533673,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs564853747","seq_region_name":"7","source":"dbSNP","start":140533674,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140533674,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1259812360","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140533675,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533675,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140533676,"alleles":["G","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533676,"clinical_significance":[],"id":"rs114627810","seq_region_name":"7"},{"alleles":["C","G","T"],"end":140533680,"strand":1,"feature_type":"variation","start":140533680,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs754530514","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533681,"source":"dbSNP","strand":1,"feature_type":"variation","end":140533681,"alleles":["G","A"],"id":"rs544083416","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs10254654","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140533690,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533690,"source":"dbSNP"},{"start":140533694,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C"],"end":140533694,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs933686824","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130488712","alleles":["C","A"],"end":140533695,"feature_type":"variation","strand":1,"source":"dbSNP","start":140533695,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs529840123","end":140533700,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140533700,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs910976779","source":"dbSNP","start":140533701,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140533701,"alleles":["G","A"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140533702,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533702,"source":"dbSNP","id":"rs186562225","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","A"],"end":140533703,"feature_type":"variation","strand":1,"source":"dbSNP","start":140533703,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs560547811"},{"end":140533707,"alleles":["GGG","GG"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140533705,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1444393610"},{"seq_region_name":"7","id":"rs1796352711","clinical_significance":[],"start":140533706,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140533706,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs942394397","clinical_significance":[],"strand":1,"feature_type":"variation","end":140533710,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533710,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140533713,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533713,"source":"dbSNP","seq_region_name":"7","id":"rs1796352942","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1406852364","end":140533714,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140533714,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130488813","alleles":["C","A"],"end":140533716,"feature_type":"variation","strand":1,"source":"dbSNP","start":140533716,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs918464282","clinical_significance":[],"start":140533718,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G","T"],"end":140533718,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1043614780","end":140533719,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140533719,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796353233","end":140533724,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140533724,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["A","G"],"end":140533727,"strand":1,"feature_type":"variation","start":140533727,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs955174583","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796353408","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533728,"source":"dbSNP","strand":1,"feature_type":"variation","end":140533728,"alleles":["C","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533728,"source":"dbSNP","strand":1,"feature_type":"variation","end":140533736,"alleles":["CTATCTCCT","CT"],"seq_region_name":"7","id":"rs759168760","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs527709205","source":"dbSNP","start":140533731,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140533731,"alleles":["T","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1796353692","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140533736,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533736,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140533741,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533741,"clinical_significance":[],"seq_region_name":"7","id":"rs540595772"},{"seq_region_name":"7","id":"rs2130488907","clinical_significance":[],"alleles":["TTTGTTTTG","TTTG"],"end":140533753,"strand":1,"feature_type":"variation","start":140533745,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140533748,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533748,"clinical_significance":[],"seq_region_name":"7","id":"rs764789466"},{"start":140533752,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140533752,"alleles":["T","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1331039985","clinical_significance":[]},{"alleles":["G","A"],"end":140533755,"strand":1,"feature_type":"variation","start":140533755,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs752185686","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533760,"source":"dbSNP","strand":1,"feature_type":"variation","end":140533760,"alleles":["C","T"],"seq_region_name":"7","id":"rs1796354197","clinical_significance":[]},{"start":140533761,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140533761,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1240035408","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585567478","clinical_significance":[],"start":140533764,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140533764,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140533766,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533766,"source":"dbSNP","id":"rs1406399515","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1457417685","clinical_significance":[],"end":140533767,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140533767,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533771,"feature_type":"variation","strand":1,"end":140533771,"alleles":["G","A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1247777593"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533772,"source":"dbSNP","strand":1,"feature_type":"variation","end":140533772,"alleles":["T","A"],"id":"rs1796354780","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533781,"feature_type":"variation","strand":1,"end":140533781,"alleles":["C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585567517"},{"seq_region_name":"7","id":"rs1449726620","clinical_significance":[],"start":140533782,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140533782,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140533783,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533783,"clinical_significance":[],"id":"rs1300620533","seq_region_name":"7"},{"source":"dbSNP","start":140533785,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140533785,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs10254777"},{"source":"dbSNP","start":140533786,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140533786,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796355388"},{"source":"dbSNP","start":140533788,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140533788,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1289643813"},{"source":"dbSNP","start":140533789,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140533789,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs571162264"},{"start":140533790,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140533790,"alleles":["T","A"],"strand":1,"feature_type":"variation","id":"rs942591552","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140533791,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140533791,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1280020134","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1443916490","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533794,"source":"dbSNP","strand":1,"feature_type":"variation","end":140533794,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1054465938","clinical_significance":[],"start":140533795,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140533795,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533796,"source":"dbSNP","strand":1,"feature_type":"variation","end":140533796,"alleles":["T","C"],"id":"rs1796356091","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","T"],"end":140533798,"feature_type":"variation","strand":1,"source":"dbSNP","start":140533798,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs914547483"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533802,"feature_type":"variation","strand":1,"end":140533802,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1796356295"},{"source":"dbSNP","start":140533807,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140533807,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1294005186","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533809,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140533809,"seq_region_name":"7","id":"rs1217813024","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796356549","clinical_significance":[],"start":140533811,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AATA","A"],"end":140533814,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140533813,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140533813,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1052349188","seq_region_name":"7"},{"start":140533815,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140533815,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1347848580","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1302316310","source":"dbSNP","start":140533818,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140533818,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1420153122","clinical_significance":[],"start":140533819,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140533819,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1796357038","clinical_significance":[],"strand":1,"feature_type":"variation","end":140533820,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533820,"source":"dbSNP"},{"source":"dbSNP","start":140533823,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140533823,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1585567661","seq_region_name":"7"},{"clinical_significance":[],"id":"rs2130489174","seq_region_name":"7","feature_type":"variation","strand":1,"end":140533825,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533825},{"start":140533826,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140533826,"strand":1,"feature_type":"variation","id":"rs946172438","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533829,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140533829,"id":"rs1312692051","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1263487929","source":"dbSNP","start":140533832,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140533832,"alleles":["C","A"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533837,"source":"dbSNP","strand":1,"feature_type":"variation","end":140533837,"alleles":["A","G"],"seq_region_name":"7","id":"rs1157136780","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140533838,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533838,"clinical_significance":[],"seq_region_name":"7","id":"rs1418547966"},{"seq_region_name":"7","id":"rs1796357660","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533842,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140533842},{"seq_region_name":"7","id":"rs1041764052","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533844,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C","T"],"end":140533844},{"seq_region_name":"7","id":"rs1796357934","clinical_significance":[],"end":140533845,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140533845,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140533847,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140533847,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs896364432"},{"end":140533854,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140533854,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs538576546","clinical_significance":[]},{"clinical_significance":[],"id":"rs574220252","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533856,"feature_type":"variation","strand":1,"end":140533856,"alleles":["A","G"]},{"alleles":["T","C"],"end":140533858,"feature_type":"variation","strand":1,"source":"dbSNP","start":140533858,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1443257635"},{"clinical_significance":[],"seq_region_name":"7","id":"rs550196459","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140533860,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533860},{"alleles":["G","A"],"end":140533861,"strand":1,"feature_type":"variation","start":140533861,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1235863103","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533862,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140533862,"seq_region_name":"7","id":"rs1003009098","clinical_significance":[]},{"alleles":["C","-"],"end":140533863,"feature_type":"variation","strand":1,"source":"dbSNP","start":140533863,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796358724"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140533865,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533865,"clinical_significance":[],"seq_region_name":"7","id":"rs1796358814"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140533869,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533869,"source":"dbSNP","seq_region_name":"7","id":"rs1796358894","clinical_significance":[]},{"source":"dbSNP","start":140533870,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140533870,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1024684553","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1056343500","source":"dbSNP","start":140533874,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140533874,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1585567810","clinical_significance":[],"start":140533878,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140533878,"alleles":["T","A","G"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140533885,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533885,"clinical_significance":[],"seq_region_name":"7","id":"rs1585567823"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130489348","feature_type":"variation","strand":1,"end":140533888,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533888},{"end":140533890,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140533890,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796359371"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796359463","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533892,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140533892},{"seq_region_name":"7","id":"rs138550840","clinical_significance":[],"alleles":["C","G"],"end":140533893,"strand":1,"feature_type":"variation","start":140533893,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["C","T"],"end":140533895,"feature_type":"variation","strand":1,"source":"dbSNP","start":140533895,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796359687"},{"id":"rs535648101","seq_region_name":"7","clinical_significance":[],"alleles":["T","A","C"],"end":140533896,"strand":1,"feature_type":"variation","start":140533896,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1796359914","seq_region_name":"7","clinical_significance":[],"alleles":["T","A"],"end":140533897,"strand":1,"feature_type":"variation","start":140533897,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796359998","alleles":["C","T"],"end":140533899,"feature_type":"variation","strand":1,"source":"dbSNP","start":140533899,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140533900,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533900,"clinical_significance":[],"id":"rs554669203","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140533904,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533904,"clinical_significance":[],"seq_region_name":"7","id":"rs1796360184"},{"clinical_significance":[],"id":"rs1585567869","seq_region_name":"7","end":140533910,"alleles":["T","A","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140533910,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs146264406","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140533911,"strand":1,"feature_type":"variation","start":140533911,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140533912,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140533912,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs6951170","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140533915,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533915,"clinical_significance":[],"id":"rs1265993577","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1001564254","clinical_significance":[],"start":140533917,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140533917,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1017082768","clinical_significance":[],"strand":1,"feature_type":"variation","end":140533918,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533918,"source":"dbSNP"},{"seq_region_name":"7","id":"rs771599793","clinical_significance":[],"start":140533922,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140533922,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs11766018","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533925,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140533925},{"clinical_significance":[],"seq_region_name":"7","id":"rs1178327384","feature_type":"variation","strand":1,"alleles":["C","-"],"end":140533925,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533925},{"strand":1,"feature_type":"variation","end":140533927,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533927,"source":"dbSNP","seq_region_name":"7","id":"rs1796361268","clinical_significance":[]},{"end":140533930,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140533930,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796361352","clinical_significance":[]},{"id":"rs1796361440","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140533931,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533931,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140533932,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533932,"clinical_significance":[],"id":"rs1006849412","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1796361647","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533935,"source":"dbSNP","strand":1,"feature_type":"variation","end":140533935,"alleles":["A","G"]},{"feature_type":"variation","strand":1,"end":140533936,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533936,"clinical_significance":[],"id":"rs2130489539","seq_region_name":"7"},{"end":140533937,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140533937,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1585567955","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533938,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140533938,"seq_region_name":"7","id":"rs972848356","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1415877469","source":"dbSNP","start":140533939,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140533939,"alleles":["A","T"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140533941,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533941,"source":"dbSNP","seq_region_name":"7","id":"rs774804559","clinical_significance":[]},{"seq_region_name":"7","id":"rs192384187","clinical_significance":[],"end":140533942,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140533942,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1261515781","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140533944,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533944},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563122230","source":"dbSNP","start":140533946,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140533946,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140533952,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140533952,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs772115890"},{"clinical_significance":[],"seq_region_name":"7","id":"rs775844285","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533953,"feature_type":"variation","strand":1,"end":140533953,"alleles":["G","A"]},{"start":140533955,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140533955,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796362600","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs986491060","feature_type":"variation","strand":1,"end":140533957,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533957},{"start":140533960,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140533960,"alleles":["C","CC"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1358143047","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140533963,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533963,"clinical_significance":[],"seq_region_name":"7","id":"rs1025386517"},{"clinical_significance":[],"seq_region_name":"7","id":"rs910872750","feature_type":"variation","strand":1,"end":140533968,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533968},{"source":"dbSNP","start":140533969,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140533969,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs963828836","seq_region_name":"7"},{"end":140533974,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140533974,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs964026472"},{"seq_region_name":"7","id":"rs558085078","clinical_significance":[],"start":140533975,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140533975,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1276083951","feature_type":"variation","strand":1,"end":140533976,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533976},{"clinical_significance":[],"id":"rs1338381119","seq_region_name":"7","source":"dbSNP","start":140533977,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140533977,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1796363557","seq_region_name":"7","source":"dbSNP","start":140533978,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140533978,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs567441007","alleles":["T","C"],"end":140533981,"feature_type":"variation","strand":1,"source":"dbSNP","start":140533981,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140533985,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533985,"source":"dbSNP","seq_region_name":"7","id":"rs979156382","clinical_significance":[]},{"end":140533989,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140533989,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs760657345","clinical_significance":[]},{"end":140533991,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140533991,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1796363959","seq_region_name":"7","clinical_significance":[]},{"id":"rs1585568096","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140533994,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533994,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140533995,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140533995,"clinical_significance":[],"seq_region_name":"7","id":"rs1283747601"},{"alleles":["C","T"],"end":140533998,"feature_type":"variation","strand":1,"source":"dbSNP","start":140533998,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1464586854"},{"seq_region_name":"7","id":"rs1796364327","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140533999,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140533999},{"id":"rs1346848464","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534000,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140534000},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140534001,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534001,"source":"dbSNP","seq_region_name":"7","id":"rs1405489080","clinical_significance":[]},{"alleles":["C","T"],"end":140534002,"feature_type":"variation","strand":1,"source":"dbSNP","start":140534002,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs576430779"},{"seq_region_name":"7","id":"rs563375646","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534006,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140534006},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534007,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140534007,"seq_region_name":"7","id":"rs956592878","clinical_significance":[]},{"end":140534012,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140534012,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1796364902","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1276778861","alleles":["C","A","T"],"end":140534016,"feature_type":"variation","strand":1,"source":"dbSNP","start":140534016,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534017,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140534017,"id":"rs544537957","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1311769024","seq_region_name":"7","source":"dbSNP","start":140534025,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140534025,"alleles":["T","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs928740161","source":"dbSNP","start":140534030,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140534030,"alleles":["C","T"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140534031,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534031,"clinical_significance":[],"seq_region_name":"7","id":"rs1796365445"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796365528","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534033,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140534033},{"start":140534038,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140534038,"strand":1,"feature_type":"variation","id":"rs1796365624","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796365722","end":140534039,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140534039,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["T","C"],"end":140534042,"strand":1,"feature_type":"variation","start":140534042,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs938728617","clinical_significance":[]},{"alleles":["G","A"],"end":140534044,"feature_type":"variation","strand":1,"source":"dbSNP","start":140534044,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796365933"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534044,"feature_type":"variation","strand":1,"end":140534222,"alleles":["GCTGGGATCACAGGCACGTGCCACCAATGCCTGGTTAATTTTTTTTTTTTTTTTTTTTTGAGATGGAGTCTTGCTCTGGCACCCAGGCTGGAGTGCAATGGTGCGATCTTGGCTCACTGCAACCTCTGCCTCCAGGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCGAGTTGCTGGGAT","GCTGGGAT"],"clinical_significance":[],"seq_region_name":"7","id":"rs1796366041"},{"seq_region_name":"7","id":"rs1055975734","clinical_significance":[],"alleles":["G","A"],"end":140534047,"strand":1,"feature_type":"variation","start":140534047,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1796366235","clinical_significance":[],"alleles":["G","A"],"end":140534048,"strand":1,"feature_type":"variation","start":140534048,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1459561157","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534049,"source":"dbSNP","strand":1,"feature_type":"variation","end":140534049,"alleles":["G","A"]},{"start":140534052,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140534052,"strand":1,"feature_type":"variation","id":"rs6966334","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140534060,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140534060,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs942336563"},{"end":140534061,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140534061,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1052673791","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1025042933","source":"dbSNP","start":140534066,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140534066,"alleles":["A","C"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140534069,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140534069,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796366823"},{"feature_type":"variation","strand":1,"alleles":["AA","A"],"end":140534070,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534069,"clinical_significance":[],"id":"rs1796366919","seq_region_name":"7"},{"end":140534070,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140534070,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1247720169"},{"source":"dbSNP","start":140534073,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140534073,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796367113"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796367220","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140534074,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534074},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796367312","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534075,"feature_type":"variation","strand":1,"end":140534075,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs574603774","clinical_significance":[],"end":140534076,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140534076,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140534077,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534077,"source":"dbSNP","seq_region_name":"7","id":"rs1226402209","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796367630","alleles":["T","G"],"end":140534079,"feature_type":"variation","strand":1,"source":"dbSNP","start":140534079,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534079,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TAATTTTTTTTTTTTTTTTTTTTTGAGATGGAGTCTTGCTCTGGCACCCAGGCTGGAGTGCAATGGTGCGATCTTGGCTCACTGCAACCTCTGCCTCCAGGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCGAGTTGCTGGGATTACAGGCACGTGCCACCACGCCCAGCTAATTTTT","TAATTTTT"],"end":140534256,"id":"rs1796367726","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796367827","clinical_significance":[],"start":140534080,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140534080,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1479209845","clinical_significance":[],"strand":1,"feature_type":"variation","end":140534080,"alleles":["-","C","T","TTTTTTTTTTTTTTT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534081,"source":"dbSNP"},{"end":140534081,"alleles":["A","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140534081,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1292340620"},{"strand":1,"feature_type":"variation","alleles":["-","AT"],"end":140534081,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534082,"source":"dbSNP","id":"rs1796368215","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796368306","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534082,"source":"dbSNP","strand":1,"feature_type":"variation","end":140534082,"alleles":["T","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796368392","alleles":["T","TATTTTTTTTTTTTT"],"end":140534082,"feature_type":"variation","strand":1,"source":"dbSNP","start":140534082,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140534082,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140534083,"alleles":["TT","TTCTTTTTTTTTTTTTTT"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796368481","clinical_significance":[]},{"clinical_significance":[],"id":"rs3042407","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534082,"feature_type":"variation","strand":1,"alleles":["TTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTT","TTTTTTTTTTT","TTTTTTTTTTTTT","TTTTTTTTTTTTTT","TTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT"],"end":140534102},{"id":"rs1189779400","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534083,"source":"dbSNP","strand":1,"feature_type":"variation","end":140534083,"alleles":["T","A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1488660962","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140534084,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534084},{"source":"dbSNP","start":140534088,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140534088,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796369823"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534089,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140534089,"seq_region_name":"7","id":"rs1796369918","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796370010","source":"dbSNP","start":140534089,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140534089,"alleles":["T","TCT"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1796370099","clinical_significance":[],"start":140534090,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140534090,"strand":1,"feature_type":"variation"},{"id":"rs2130490235","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","TCT"],"end":140534093,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534093,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534095,"source":"dbSNP","strand":1,"feature_type":"variation","end":140534103,"alleles":["TTTTTTTTG","-"],"seq_region_name":"7","id":"rs1796370201","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796370282","clinical_significance":[],"alleles":["T","C"],"end":140534096,"strand":1,"feature_type":"variation","start":140534096,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1267014367","clinical_significance":[],"start":140534096,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TTTTTTTG","-"],"end":140534103,"strand":1,"feature_type":"variation"},{"id":"rs1243972819","seq_region_name":"7","clinical_significance":[],"alleles":["TTTTTG","-"],"end":140534103,"strand":1,"feature_type":"variation","start":140534098,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1358993721","alleles":["TTTTG","-"],"end":140534103,"feature_type":"variation","strand":1,"source":"dbSNP","start":140534099,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1159977927","clinical_significance":[],"start":140534100,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TTTG","-"],"end":140534103,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140534102,"alleles":["TT","TTTTTTTTTTTTTTTTTTTTCTT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534101,"source":"dbSNP","seq_region_name":"7","id":"rs1796370723","clinical_significance":[]},{"source":"dbSNP","start":140534101,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TTG","-"],"end":140534103,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs898193861"},{"alleles":["TG","-"],"end":140534103,"feature_type":"variation","strand":1,"source":"dbSNP","start":140534102,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1491349201","seq_region_name":"7"},{"id":"rs1491445966","seq_region_name":"7","clinical_significance":[],"start":140534103,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["-","TTTTTTTTTTTTTTA","TTTTTTTTTTTTTTTA","TTTTTTTTTTTTTTTTA","TTTTTTTTTTTTTTTTGGTGG","TTTTTTTTTTTTTTTTTA","TTTTTTTTTTTTTTTTTTA","TTTTTTTTTTTTTTTTTTG","TTTTTTTTTTTTTTTTTTGGTG","TTTTTTTTTTTTTTTTTTTG","TTTTTTTTTTTTTTTTTTTTTA"],"end":140534102,"strand":1,"feature_type":"variation"},{"start":140534103,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140534103,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs66783039","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534103,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","-"],"end":140534103,"seq_region_name":"7","id":"rs869236947","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130490360","feature_type":"variation","strand":1,"alleles":["GAGA","GA"],"end":140534106,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534103},{"feature_type":"variation","strand":1,"end":140534104,"alleles":["A","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534104,"clinical_significance":[],"seq_region_name":"7","id":"rs1796371288"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534105,"feature_type":"variation","strand":1,"alleles":["-","TTTT","TTTTTTTTTTTTTTT"],"end":140534104,"clinical_significance":[],"seq_region_name":"7","id":"rs1796371383"},{"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140534105,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534105,"source":"dbSNP","seq_region_name":"7","id":"rs1796371490","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796371602","clinical_significance":[],"start":140534106,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140534106,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585568509","source":"dbSNP","start":140534110,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140534110,"alleles":["A","G"],"feature_type":"variation","strand":1},{"end":140534112,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140534112,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1292150012"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1424500894","alleles":["G","A"],"end":140534116,"feature_type":"variation","strand":1,"source":"dbSNP","start":140534116,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["A","G"],"end":140534124,"feature_type":"variation","strand":1,"source":"dbSNP","start":140534124,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796371957"},{"strand":1,"feature_type":"variation","end":140534126,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534126,"source":"dbSNP","seq_region_name":"7","id":"rs993848809","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796372178","clinical_significance":[],"start":140534128,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140534128,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1585568548","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534129,"source":"dbSNP","strand":1,"feature_type":"variation","end":140534129,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2363831","end":140534131,"alleles":["C","A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140534131,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1796372517","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534132,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140534132},{"clinical_significance":[],"id":"rs1303684839","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534137,"feature_type":"variation","strand":1,"end":140534137,"alleles":["T","A","G"]},{"source":"dbSNP","start":140534137,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","-"],"end":140534137,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1796372735","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796372827","source":"dbSNP","start":140534139,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140534139,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1796372918","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534140,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140534140},{"seq_region_name":"7","id":"rs2130490512","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140534141,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534141,"source":"dbSNP"},{"end":140534142,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140534142,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1796373020","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140534143,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534143,"source":"dbSNP","seq_region_name":"7","id":"rs10237732","clinical_significance":[]},{"end":140534144,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140534144,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs139213102","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534147,"feature_type":"variation","strand":1,"end":140534147,"alleles":["C","G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1452119340"},{"seq_region_name":"7","id":"rs905856728","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140534148,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534148,"source":"dbSNP"},{"source":"dbSNP","start":140534150,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140534150,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1490140358"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534152,"feature_type":"variation","strand":1,"end":140534152,"alleles":["T","C"],"clinical_significance":[],"id":"rs2130490581","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140534159,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534159,"clinical_significance":[],"id":"rs1286976152","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140534162,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534162,"clinical_significance":[],"seq_region_name":"7","id":"rs1796373882"},{"clinical_significance":[],"id":"rs1585568627","seq_region_name":"7","feature_type":"variation","strand":1,"end":140534165,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534165},{"clinical_significance":[],"seq_region_name":"7","id":"rs1219112455","source":"dbSNP","start":140534166,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140534166,"alleles":["C","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs2130490620","clinical_significance":[],"start":140534167,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140534167,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1348569264","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140534169,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534169},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140534171,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534171,"source":"dbSNP","seq_region_name":"7","id":"rs1279051090","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796374357","clinical_significance":[],"strand":1,"feature_type":"variation","end":140534174,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534174,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140534177,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534177,"clinical_significance":[],"seq_region_name":"7","id":"rs1796374463"},{"alleles":["G","A"],"end":140534178,"feature_type":"variation","strand":1,"source":"dbSNP","start":140534178,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1234522698"},{"clinical_significance":[],"id":"rs1333327485","seq_region_name":"7","feature_type":"variation","strand":1,"end":140534180,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534180},{"clinical_significance":[],"seq_region_name":"7","id":"rs1281993386","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534184,"feature_type":"variation","strand":1,"end":140534184,"alleles":["A","G"]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140534186,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534186,"source":"dbSNP","seq_region_name":"7","id":"rs1404698392","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796374958","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534187,"source":"dbSNP","strand":1,"feature_type":"variation","end":140534187,"alleles":["T","C"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534194,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140534194,"clinical_significance":[],"seq_region_name":"7","id":"rs1796375049"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1001604911","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534197,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140534197},{"seq_region_name":"7","id":"rs1796375255","clinical_significance":[],"strand":1,"feature_type":"variation","end":140534198,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534198,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534201,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140534201,"clinical_significance":[],"seq_region_name":"7","id":"rs1273980369"},{"seq_region_name":"7","id":"rs1585568714","clinical_significance":[],"start":140534203,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140534203,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1038432899","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534209,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140534209},{"clinical_significance":[],"seq_region_name":"7","id":"rs1241117513","end":140534210,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140534210,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1157481708","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140534213,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534213},{"source":"dbSNP","start":140534214,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140534214,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1478104177"},{"source":"dbSNP","start":140534215,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140534215,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1379279895"},{"seq_region_name":"7","id":"rs898564774","clinical_significance":[],"end":140534216,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140534216,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1288321692","clinical_significance":[],"end":140534221,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140534221,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140534222,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140534222,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1197243042","seq_region_name":"7"},{"seq_region_name":"7","id":"rs141719740","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140534227,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534227,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1796376539","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534228,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GCACGTGCCACCACGCCCAGC","GC"],"end":140534248},{"strand":1,"feature_type":"variation","end":140534229,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534229,"source":"dbSNP","seq_region_name":"7","id":"rs531589656","clinical_significance":[]},{"seq_region_name":"7","id":"rs550474874","clinical_significance":[],"strand":1,"feature_type":"variation","end":140534230,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534230,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1453781038","alleles":["C","A","T"],"end":140534231,"feature_type":"variation","strand":1,"source":"dbSNP","start":140534231,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs568629672","clinical_significance":[],"start":140534232,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140534232,"alleles":["G","A","C"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534234,"source":"dbSNP","strand":1,"feature_type":"variation","end":140534234,"alleles":["G","A"],"seq_region_name":"7","id":"rs1347279292","clinical_significance":[]},{"seq_region_name":"7","id":"rs1261780071","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534235,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140534235},{"feature_type":"variation","strand":1,"alleles":["CC","C"],"end":140534239,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534238,"clinical_significance":[],"id":"rs1563122475","seq_region_name":"7"},{"end":140534241,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140534241,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs955684817"},{"start":140534242,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140534242,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs1796377553","seq_region_name":"7","clinical_significance":[]},{"id":"rs1341462176","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140534244,"strand":1,"feature_type":"variation","start":140534244,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1008894015","clinical_significance":[],"alleles":["A","G"],"end":140534246,"strand":1,"feature_type":"variation","start":140534246,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1432370988","end":140534253,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140534253,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","T"],"end":140534262,"feature_type":"variation","strand":1,"source":"dbSNP","start":140534262,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1585568873","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1021972212","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140534263,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534263,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1796378460","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140534265,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534265,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140534271,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534271,"source":"dbSNP","seq_region_name":"7","id":"rs1180113137","clinical_significance":[]},{"seq_region_name":"7","id":"rs529504110","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534273,"source":"dbSNP","strand":1,"feature_type":"variation","end":140534273,"alleles":["C","T"]},{"source":"dbSNP","start":140534274,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140534274,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1438545844"},{"clinical_significance":[],"seq_region_name":"7","id":"rs963693988","source":"dbSNP","start":140534275,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140534275,"feature_type":"variation","strand":1},{"start":140534277,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140534277,"strand":1,"feature_type":"variation","id":"rs977393677","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs979063057","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534283,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140534283},{"seq_region_name":"7","id":"rs925042653","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534285,"source":"dbSNP","strand":1,"feature_type":"variation","end":140534285,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796379805","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534289,"feature_type":"variation","strand":1,"end":140534289,"alleles":["T","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs956401599","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534291,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140534291},{"clinical_significance":[],"seq_region_name":"7","id":"rs928605841","end":140534292,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140534292,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140534293,"alleles":["-","AGGA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140534294,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1403503665"},{"alleles":["T","A"],"end":140534294,"strand":1,"feature_type":"variation","start":140534294,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs184721486","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1241720814","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534295,"feature_type":"variation","strand":1,"end":140534295,"alleles":["G","T"]},{"id":"rs374576935","seq_region_name":"7","clinical_significance":[],"start":140534297,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140534297,"alleles":["C","G","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1354883340","clinical_significance":[],"alleles":["CTTATC","-"],"end":140534302,"strand":1,"feature_type":"variation","start":140534297,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796381061","end":140534298,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140534298,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1188555192","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534299,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140534299},{"start":140534304,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G","T"],"end":140534304,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1444162601","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1203520765","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534306,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140534306},{"clinical_significance":[],"id":"rs1311741814","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","T"],"end":140534307,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534307},{"end":140534308,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140534308,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796382192"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796382339","alleles":["G","T"],"end":140534313,"feature_type":"variation","strand":1,"source":"dbSNP","start":140534313,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140534317,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534317,"clinical_significance":[],"id":"rs1319214065","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1374870909","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534319,"feature_type":"variation","strand":1,"alleles":["A","C","T"],"end":140534319},{"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140534320,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534320,"clinical_significance":[],"seq_region_name":"7","id":"rs1213157856"},{"seq_region_name":"7","id":"rs1339186973","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534325,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","TT"],"end":140534325},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140534326,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534326,"clinical_significance":[],"seq_region_name":"7","id":"rs1796383112"},{"alleles":["C","T"],"end":140534328,"strand":1,"feature_type":"variation","start":140534328,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs566234826","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796383424","clinical_significance":[],"start":140534329,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140534329,"strand":1,"feature_type":"variation"},{"end":140534330,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140534330,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796383563","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1481909159","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534333,"feature_type":"variation","strand":1,"alleles":["T","A","G"],"end":140534333},{"seq_region_name":"7","id":"rs1796383840","clinical_significance":[],"alleles":["C","T"],"end":140534337,"strand":1,"feature_type":"variation","start":140534337,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534338,"feature_type":"variation","strand":1,"end":140534338,"alleles":["C","T"],"clinical_significance":[],"id":"rs1448331663","seq_region_name":"7"},{"end":140534341,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140534341,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796384158","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796384292","clinical_significance":[],"strand":1,"feature_type":"variation","end":140534346,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534346,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1384291164","clinical_significance":[],"strand":1,"feature_type":"variation","end":140534351,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534351,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140534358,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534358,"clinical_significance":[],"id":"rs1796384587","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140534360,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534360,"source":"dbSNP","id":"rs1796384737","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534362,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140534362,"id":"rs368524343","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140534363,"alleles":["A","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534363,"source":"dbSNP","id":"rs991980616","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1284811609","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534365,"feature_type":"variation","strand":1,"end":140534365,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs917732841","feature_type":"variation","strand":1,"end":140534367,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534367},{"id":"rs949367770","seq_region_name":"7","clinical_significance":[],"alleles":["C","A","T"],"end":140534368,"strand":1,"feature_type":"variation","start":140534368,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140534373,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140534373,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1208557159"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1045374135","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534374,"feature_type":"variation","strand":1,"end":140534374,"alleles":["C","A","G","T"]},{"alleles":["G","A"],"end":140534375,"strand":1,"feature_type":"variation","start":140534375,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585569153","clinical_significance":[]},{"alleles":["G","A"],"end":140534380,"feature_type":"variation","strand":1,"source":"dbSNP","start":140534380,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796386095"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534381,"feature_type":"variation","strand":1,"end":140534381,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1796386258"},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140534382,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534382,"clinical_significance":[],"id":"rs1796386431","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1163997588","clinical_significance":[],"start":140534386,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140534386,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1796386737","clinical_significance":[],"strand":1,"feature_type":"variation","end":140534387,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534387,"source":"dbSNP"},{"alleles":["A","T"],"end":140534389,"feature_type":"variation","strand":1,"source":"dbSNP","start":140534389,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs942181075"},{"clinical_significance":[],"seq_region_name":"7","id":"rs754870550","alleles":["A","G"],"end":140534390,"feature_type":"variation","strand":1,"source":"dbSNP","start":140534390,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["A","G"],"end":140534397,"feature_type":"variation","strand":1,"source":"dbSNP","start":140534397,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796387168"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534402,"source":"dbSNP","strand":1,"feature_type":"variation","end":140534402,"alleles":["C","T"],"seq_region_name":"7","id":"rs780696406","clinical_significance":[]},{"id":"rs1796387431","seq_region_name":"7","clinical_significance":[],"alleles":["A","G"],"end":140534404,"strand":1,"feature_type":"variation","start":140534404,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140534409,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140534409,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796387560"},{"strand":1,"feature_type":"variation","end":140534413,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534413,"source":"dbSNP","seq_region_name":"7","id":"rs1183056267","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796387820","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534415,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140534415},{"clinical_significance":[],"id":"rs1458313219","seq_region_name":"7","source":"dbSNP","start":140534418,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140534418,"feature_type":"variation","strand":1},{"id":"rs1240542083","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534419,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140534419},{"clinical_significance":[],"seq_region_name":"7","id":"rs1458491757","source":"dbSNP","start":140534420,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140534420,"alleles":["C","-"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534427,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140534427,"seq_region_name":"7","id":"rs1585569222","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1437564372","source":"dbSNP","start":140534435,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140534437,"alleles":["AAA","AA"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs937363017","end":140534439,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140534439,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1796388849","clinical_significance":[],"start":140534440,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140534440,"strand":1,"feature_type":"variation"},{"alleles":["G","A"],"end":140534442,"strand":1,"feature_type":"variation","start":140534442,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs781129348","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140534455,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534455,"source":"dbSNP","seq_region_name":"7","id":"rs1361148019","clinical_significance":[]},{"end":140534460,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140534460,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796389306","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796389454","clinical_significance":[],"alleles":["C","A"],"end":140534462,"strand":1,"feature_type":"variation","start":140534462,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["A","-"],"end":140534463,"strand":1,"feature_type":"variation","start":140534463,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1585569266","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140534464,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","GG"],"end":140534464,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585569274"},{"seq_region_name":"7","id":"rs1182242907","clinical_significance":[],"strand":1,"feature_type":"variation","end":140534465,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534465,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140534466,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534466,"source":"dbSNP","seq_region_name":"7","id":"rs1312540920","clinical_significance":[]},{"clinical_significance":[],"id":"rs898594114","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534468,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140534468},{"clinical_significance":[],"seq_region_name":"7","id":"rs1244568979","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140534474,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534474},{"id":"rs1377045418","seq_region_name":"7","clinical_significance":[],"alleles":["A","C"],"end":140534475,"strand":1,"feature_type":"variation","start":140534475,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs574990216","clinical_significance":[],"strand":1,"feature_type":"variation","end":140534476,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534476,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["AAATAAAT","AAAT"],"end":140534483,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534476,"source":"dbSNP","seq_region_name":"7","id":"rs373282138","clinical_significance":[]},{"end":140534479,"alleles":["T","A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140534479,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1353641938","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140534482,"alleles":["AAA","AA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534480,"source":"dbSNP","seq_region_name":"7","id":"rs898099046","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585569370","alleles":["T","A"],"end":140534483,"feature_type":"variation","strand":1,"source":"dbSNP","start":140534483,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1457006182","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534488,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140534488},{"id":"rs1047267111","seq_region_name":"7","clinical_significance":[],"end":140534490,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140534490,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1187680623","seq_region_name":"7","clinical_significance":[],"end":140534493,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140534493,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140534498,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534498,"clinical_significance":[],"seq_region_name":"7","id":"rs1698441325"},{"seq_region_name":"7","id":"rs1796391621","clinical_significance":[],"strand":1,"feature_type":"variation","end":140534499,"alleles":["GG","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534498,"source":"dbSNP"},{"start":140534499,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140534499,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1426384305","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140534503,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534503,"clinical_significance":[],"id":"rs1796391892","seq_region_name":"7"},{"end":140534514,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140534514,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1369667751","clinical_significance":[]},{"seq_region_name":"7","id":"rs929507243","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534515,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140534515},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140534516,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534516,"source":"dbSNP","id":"rs1796392325","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1162579842","source":"dbSNP","start":140534517,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140534517,"alleles":["T","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs533690314","source":"dbSNP","start":140534519,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140534519,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140534534,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534534,"clinical_significance":[],"seq_region_name":"7","id":"rs1299687385"},{"seq_region_name":"7","id":"rs868270892","clinical_significance":[],"alleles":["T","C"],"end":140534537,"strand":1,"feature_type":"variation","start":140534537,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140534539,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140534539,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1796393039","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130491720","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534543,"feature_type":"variation","strand":1,"end":140534543,"alleles":["T","C"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534553,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140534553,"clinical_significance":[],"id":"rs1796393185","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534554,"source":"dbSNP","strand":1,"feature_type":"variation","end":140534554,"alleles":["T","C"],"id":"rs891271600","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796393469","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534558,"source":"dbSNP","strand":1,"feature_type":"variation","end":140534558,"alleles":["A","C"]},{"id":"rs1796393596","seq_region_name":"7","clinical_significance":[],"start":140534561,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140534561,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140534562,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140534562,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs745856744","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796393897","feature_type":"variation","strand":1,"end":140534567,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534567},{"seq_region_name":"7","id":"rs1018549613","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140534573,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534573,"source":"dbSNP"},{"start":140534575,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140534575,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796394186","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1410291662","source":"dbSNP","start":140534577,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140534577,"alleles":["C","A"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534579,"source":"dbSNP","strand":1,"feature_type":"variation","end":140534579,"alleles":["C","T"],"seq_region_name":"7","id":"rs964265688","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534580,"feature_type":"variation","strand":1,"end":140534580,"alleles":["G","A"],"clinical_significance":[],"id":"rs752447194","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1007998328","clinical_significance":[],"start":140534581,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140534581,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs558223897","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534585,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140534585},{"clinical_significance":[],"seq_region_name":"7","id":"rs1489975432","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534586,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140534586},{"clinical_significance":[],"id":"rs1796395227","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534587,"feature_type":"variation","strand":1,"end":140534587,"alleles":["C","T"]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140534593,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534593,"clinical_significance":[],"id":"rs1796395373","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1796395539","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140534595,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534595,"source":"dbSNP"},{"id":"rs1328984062","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140534600,"alleles":["GGGGG","GGGGGG"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534596,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["G","C","T"],"end":140534599,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534599,"source":"dbSNP","id":"rs899550622","seq_region_name":"7","clinical_significance":[]},{"end":140534600,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140534600,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs150562510","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140534604,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534604,"source":"dbSNP","seq_region_name":"7","id":"rs1308529762","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs988291989","source":"dbSNP","start":140534607,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140534607,"feature_type":"variation","strand":1},{"alleles":["G","A"],"end":140534611,"feature_type":"variation","strand":1,"source":"dbSNP","start":140534611,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1011842553"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796396462","feature_type":"variation","strand":1,"end":140534614,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534614},{"seq_region_name":"7","id":"rs1372518210","clinical_significance":[],"end":140534617,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140534617,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796396654","source":"dbSNP","start":140534620,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140534620,"alleles":["G","A"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534622,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140534622,"clinical_significance":[],"seq_region_name":"7","id":"rs1391007301"},{"source":"dbSNP","start":140534646,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140534646,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1334991402"},{"end":140534647,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140534647,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1021374386"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534655,"source":"dbSNP","strand":1,"feature_type":"variation","end":140534655,"alleles":["A","T"],"seq_region_name":"7","id":"rs2130491992","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796397115","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534662,"source":"dbSNP","strand":1,"feature_type":"variation","end":140534662,"alleles":["C","T"]},{"end":140534667,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140534667,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796397210"},{"seq_region_name":"7","id":"rs1796397303","clinical_significance":[],"alleles":["T","A","C"],"end":140534669,"strand":1,"feature_type":"variation","start":140534669,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1342330359","clinical_significance":[],"start":140534671,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140534671,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1024831020","feature_type":"variation","strand":1,"end":140534676,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534676},{"source":"dbSNP","start":140534678,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140534678,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796397602"},{"source":"dbSNP","start":140534682,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140534682,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796397685"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534689,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140534689,"seq_region_name":"7","id":"rs970982723","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1420558144","end":140534692,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140534692,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140534693,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534693,"clinical_significance":[],"seq_region_name":"7","id":"rs980608699"},{"end":140534698,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140534698,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs926547336","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796398148","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140534699,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534699,"source":"dbSNP"},{"source":"dbSNP","start":140534702,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140534702,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1796398267","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1284131661","source":"dbSNP","start":140534703,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140534703,"alleles":["G","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1400255870","clinical_significance":[],"alleles":["T","C"],"end":140534706,"strand":1,"feature_type":"variation","start":140534706,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796398557","source":"dbSNP","start":140534707,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140534707,"feature_type":"variation","strand":1},{"start":140534715,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140534715,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1426460713","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585569710","end":140534719,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140534719,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140534725,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140534725,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs537422523","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796398940","clinical_significance":[],"end":140534727,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140534727,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1202274037","seq_region_name":"7","feature_type":"variation","strand":1,"end":140534732,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534732},{"seq_region_name":"7","id":"rs1796399154","clinical_significance":[],"strand":1,"feature_type":"variation","end":140534733,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534733,"source":"dbSNP"},{"alleles":["A","T"],"end":140534735,"strand":1,"feature_type":"variation","start":140534735,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1319148864","clinical_significance":[]},{"alleles":["T","C","G"],"end":140534737,"feature_type":"variation","strand":1,"source":"dbSNP","start":140534737,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585569748"},{"alleles":["T","C"],"end":140534742,"strand":1,"feature_type":"variation","start":140534742,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796399495","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796399576","clinical_significance":[],"strand":1,"feature_type":"variation","end":140534752,"alleles":["GAAGGAAGA","GA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534744,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140534750,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534750,"clinical_significance":[],"id":"rs1220876982","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140534753,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534753,"clinical_significance":[],"seq_region_name":"7","id":"rs1268651395"},{"feature_type":"variation","strand":1,"end":140534755,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534755,"clinical_significance":[],"seq_region_name":"7","id":"rs1796399881"},{"seq_region_name":"7","id":"rs1256519796","clinical_significance":[],"alleles":["AGAAAGA","AGA"],"end":140534762,"strand":1,"feature_type":"variation","start":140534756,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796400086","source":"dbSNP","start":140534756,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AGAAAGAGA","AGA"],"end":140534764,"feature_type":"variation","strand":1},{"alleles":["A","G"],"end":140534758,"strand":1,"feature_type":"variation","start":140534758,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796400185","clinical_significance":[]},{"source":"dbSNP","start":140534759,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140534759,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796400271"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1485991157","feature_type":"variation","strand":1,"end":140534765,"alleles":["AGAGAG","AG","AGAG"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534760},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534761,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140534761,"clinical_significance":[],"seq_region_name":"7","id":"rs777380512"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130492299","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140534763,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534763},{"clinical_significance":[],"seq_region_name":"7","id":"rs1316966169","feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140534764,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534764},{"source":"dbSNP","start":140534765,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140534765,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs941918203"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534767,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140534767,"id":"rs1796400858","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796400946","source":"dbSNP","start":140534768,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140534768,"alleles":["C","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1200661226","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140534770,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534770,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140534771,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534771,"source":"dbSNP","seq_region_name":"7","id":"rs12113039","clinical_significance":[]},{"id":"rs2130492378","seq_region_name":"7","clinical_significance":[],"start":140534773,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140534773,"strand":1,"feature_type":"variation"},{"end":140534774,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140534774,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs139599530","seq_region_name":"7"},{"start":140534775,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140534775,"strand":1,"feature_type":"variation","id":"rs542010806","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1796401562","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534778,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140534778},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534781,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140534781,"clinical_significance":[],"id":"rs1796401661","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1796401762","clinical_significance":[],"start":140534788,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140534788,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1263841889","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534790,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140534790},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534792,"source":"dbSNP","strand":1,"feature_type":"variation","end":140534792,"alleles":["C","T"],"seq_region_name":"7","id":"rs1796401954","clinical_significance":[]},{"id":"rs1478738556","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140534793,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534793,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140534794,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534794,"source":"dbSNP","seq_region_name":"7","id":"rs1047576532","clinical_significance":[]},{"source":"dbSNP","start":140534797,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140534797,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs73165408"},{"alleles":["T","C"],"end":140534798,"feature_type":"variation","strand":1,"source":"dbSNP","start":140534798,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs944221568"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534800,"feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140534800,"clinical_significance":[],"seq_region_name":"7","id":"rs1359847554"},{"seq_region_name":"7","id":"rs779173335","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140534802,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534802,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1468712681","alleles":["A","C"],"end":140534803,"feature_type":"variation","strand":1,"source":"dbSNP","start":140534803,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1796402841","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534807,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140534807},{"feature_type":"variation","strand":1,"end":140534809,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534809,"clinical_significance":[],"seq_region_name":"7","id":"rs2130492555"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140534814,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534814,"clinical_significance":[],"id":"rs149756963","seq_region_name":"7"},{"start":140534815,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140534815,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs900090485","clinical_significance":[]},{"seq_region_name":"7","id":"rs1171821819","clinical_significance":[],"alleles":["C","T"],"end":140534816,"strand":1,"feature_type":"variation","start":140534816,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534821,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140534821,"id":"rs1796403222","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796403325","alleles":["C","T"],"end":140534823,"feature_type":"variation","strand":1,"source":"dbSNP","start":140534823,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140534825,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140534825,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130492603","clinical_significance":[]},{"seq_region_name":"7","id":"rs1430720522","clinical_significance":[],"start":140534826,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140534826,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"end":140534830,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140534830,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1001107317","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796403600","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534836,"source":"dbSNP","strand":1,"feature_type":"variation","end":140534837,"alleles":["AA","A"]},{"seq_region_name":"7","id":"rs1796403702","clinical_significance":[],"start":140534838,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C","G"],"end":140534838,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1263378726","clinical_significance":[],"start":140534838,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140534839,"alleles":["TT","T"],"strand":1,"feature_type":"variation"},{"start":140534841,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140534841,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796403923","clinical_significance":[]},{"id":"rs561622588","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534844,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AAAA","AAA"],"end":140534847},{"clinical_significance":[],"seq_region_name":"7","id":"rs1485233423","source":"dbSNP","start":140534847,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140534847,"alleles":["A","G"],"feature_type":"variation","strand":1},{"alleles":["T","A"],"end":140534849,"strand":1,"feature_type":"variation","start":140534849,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1404533479","clinical_significance":[]},{"start":140534854,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140534854,"alleles":["C","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796404328","clinical_significance":[]},{"start":140534855,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C","G"],"end":140534855,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1032048242","clinical_significance":[]},{"alleles":["G","A"],"end":140534863,"feature_type":"variation","strand":1,"source":"dbSNP","start":140534863,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796404547"},{"seq_region_name":"7","id":"rs189589750","clinical_significance":[],"alleles":["G","T"],"end":140534867,"strand":1,"feature_type":"variation","start":140534867,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1321333347","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534869,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140534869},{"clinical_significance":[],"seq_region_name":"7","id":"rs367695884","feature_type":"variation","strand":1,"end":140534871,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534871},{"start":140534874,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140534874,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796405080","clinical_significance":[]},{"id":"rs1585570036","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140534881,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534881,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1312303310","clinical_significance":[],"strand":1,"feature_type":"variation","end":140534887,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534887,"source":"dbSNP"},{"end":140534901,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140534901,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1009207697"},{"seq_region_name":"7","id":"rs1341717161","clinical_significance":[],"start":140534906,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140534906,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1025165420","clinical_significance":[],"alleles":["G","T"],"end":140534907,"strand":1,"feature_type":"variation","start":140534907,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs970466037","clinical_significance":[],"alleles":["G","A"],"end":140534915,"strand":1,"feature_type":"variation","start":140534915,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796405790","source":"dbSNP","start":140534917,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140534917,"alleles":["G","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1585570110","clinical_significance":[],"start":140534919,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140534919,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534923,"source":"dbSNP","strand":1,"feature_type":"variation","end":140534923,"alleles":["G","A"],"id":"rs564547748","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534924,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140534924,"clinical_significance":[],"seq_region_name":"7","id":"rs1563122819"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796406218","feature_type":"variation","strand":1,"end":140534953,"alleles":["GTTGGGTCCAAGGATGTTTTGCTGTTGGGT","GTTGGGT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534924},{"source":"dbSNP","start":140534928,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140534928,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130492815"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1381883082","source":"dbSNP","start":140534930,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140534930,"feature_type":"variation","strand":1},{"end":140534936,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140534936,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1033466825","clinical_significance":[]},{"start":140534937,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140534937,"strand":1,"feature_type":"variation","id":"rs1796406525","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534939,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140534939,"id":"rs1796406640","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs943713596","clinical_significance":[],"strand":1,"feature_type":"variation","end":140534945,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534945,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140534947,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534947,"clinical_significance":[],"seq_region_name":"7","id":"rs59370856"},{"feature_type":"variation","strand":1,"end":140534949,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534949,"clinical_significance":[],"seq_region_name":"7","id":"rs1796406935"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534950,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140534950,"seq_region_name":"7","id":"rs1796407040","clinical_significance":[]},{"seq_region_name":"7","id":"rs562043529","clinical_significance":[],"alleles":["G","C","T"],"end":140534955,"strand":1,"feature_type":"variation","start":140534955,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796407384","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534957,"feature_type":"variation","strand":1,"end":140534957,"alleles":["G","A"]},{"feature_type":"variation","strand":1,"end":140534958,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534958,"clinical_significance":[],"seq_region_name":"7","id":"rs1332684846"},{"end":140534963,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140534963,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs543417119","clinical_significance":[]},{"end":140534964,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140534964,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796407834","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796407992","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534965,"source":"dbSNP","strand":1,"feature_type":"variation","end":140534965,"alleles":["A","G"]},{"feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140534967,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534967,"clinical_significance":[],"seq_region_name":"7","id":"rs772142802"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534974,"source":"dbSNP","strand":1,"feature_type":"variation","end":140534974,"alleles":["G","A"],"id":"rs1286069215","seq_region_name":"7","clinical_significance":[]},{"end":140534984,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140534984,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796408487","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140534988,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534988,"source":"dbSNP","seq_region_name":"7","id":"rs1489257693","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1385556722","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534989,"feature_type":"variation","strand":1,"alleles":["ATCA","ATCAATCA"],"end":140534992},{"strand":1,"feature_type":"variation","end":140534991,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140534991,"source":"dbSNP","id":"rs562413498","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1459630986","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140534994,"feature_type":"variation","strand":1,"end":140534994,"alleles":["G","C"]},{"seq_region_name":"7","id":"rs529517876","clinical_significance":[],"alleles":["C","A","T"],"end":140534996,"strand":1,"feature_type":"variation","start":140534996,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140534997,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140534997,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs181789238","clinical_significance":[]},{"end":140535002,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140535002,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs2130493026","seq_region_name":"7","clinical_significance":[]},{"id":"rs1200659895","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140535007,"strand":1,"feature_type":"variation","start":140535007,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1796409589","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535008,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140535008},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140535013,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535013,"clinical_significance":[],"id":"rs1226882773","seq_region_name":"7"},{"source":"dbSNP","start":140535015,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140535015,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1796409741","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140535018,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535018,"source":"dbSNP","seq_region_name":"7","id":"rs2130493068","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140535021,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535021,"source":"dbSNP","seq_region_name":"7","id":"rs1360432828","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1317503848","source":"dbSNP","start":140535023,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140535023,"alleles":["C","A","G"],"feature_type":"variation","strand":1},{"start":140535025,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140535025,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1243842903","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535030,"source":"dbSNP","strand":1,"feature_type":"variation","end":140535030,"alleles":["C","A","T"],"seq_region_name":"7","id":"rs944102834","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1382175068","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535031,"feature_type":"variation","strand":1,"end":140535031,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1310571684","clinical_significance":[],"strand":1,"feature_type":"variation","end":140535033,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535033,"source":"dbSNP"},{"alleles":["T","C","G"],"end":140535036,"strand":1,"feature_type":"variation","start":140535036,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1039927751","clinical_significance":[]},{"id":"rs1796410464","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140535041,"strand":1,"feature_type":"variation","start":140535041,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535044,"feature_type":"variation","strand":1,"end":140535044,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs768895583"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796410659","feature_type":"variation","strand":1,"end":140535045,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535045},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535049,"feature_type":"variation","strand":1,"end":140535049,"alleles":["T","C"],"clinical_significance":[],"id":"rs1585570375","seq_region_name":"7"},{"alleles":["TGCT","TGCTGCT"],"end":140535052,"strand":1,"feature_type":"variation","start":140535049,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796410844","clinical_significance":[]},{"clinical_significance":[],"id":"rs1796410951","seq_region_name":"7","feature_type":"variation","strand":1,"end":140535050,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535050},{"clinical_significance":[],"seq_region_name":"7","id":"rs184663686","end":140535055,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140535055,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140535060,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140535060,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130493185","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535061,"feature_type":"variation","strand":1,"end":140535061,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1796411143"},{"end":140535063,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140535063,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796411254","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535073,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140535073,"clinical_significance":[],"seq_region_name":"7","id":"rs776636262"},{"seq_region_name":"7","id":"rs1173141106","clinical_significance":[],"start":140535074,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140535074,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1054026262","seq_region_name":"7","alleles":["G","A"],"end":140535078,"feature_type":"variation","strand":1,"source":"dbSNP","start":140535078,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140535081,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140535081,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1796411642","seq_region_name":"7"},{"alleles":["T","A","C"],"end":140535083,"feature_type":"variation","strand":1,"source":"dbSNP","start":140535083,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1365790447","seq_region_name":"7"},{"start":140535084,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140535084,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1442200859","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796411939","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535085,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140535085},{"seq_region_name":"7","id":"rs1384092763","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535090,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140535090},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796412109","source":"dbSNP","start":140535091,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140535091,"alleles":["G","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1796412208","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535093,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140535093},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140535095,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535095,"source":"dbSNP","seq_region_name":"7","id":"rs1361223300","clinical_significance":[]},{"clinical_significance":[],"id":"rs1796412398","seq_region_name":"7","source":"dbSNP","start":140535096,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140535096,"alleles":["C","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1182360233","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535097,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140535097},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140535103,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535103,"source":"dbSNP","id":"rs761888053","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535103,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CTCTCT","CTCT"],"end":140535108,"id":"rs1796412684","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535104,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140535104,"clinical_significance":[],"seq_region_name":"7","id":"rs1248410001"},{"seq_region_name":"7","id":"rs959956441","clinical_significance":[],"start":140535105,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140535105,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs76287700","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535110,"feature_type":"variation","strand":1,"end":140535110,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1294180078","end":140535121,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140535121,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535122,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140535122,"clinical_significance":[],"seq_region_name":"7","id":"rs1796413189"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796413276","feature_type":"variation","strand":1,"end":140535127,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535127},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796413368","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535128,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140535128},{"seq_region_name":"7","id":"rs1220574893","clinical_significance":[],"start":140535132,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140535132,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1358748276","clinical_significance":[],"alleles":["G","T"],"end":140535135,"strand":1,"feature_type":"variation","start":140535135,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1280215742","clinical_significance":[],"strand":1,"feature_type":"variation","end":140535139,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535139,"source":"dbSNP"},{"start":140535153,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140535153,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","id":"rs551881962","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1387732348","feature_type":"variation","strand":1,"end":140535159,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535159},{"strand":1,"feature_type":"variation","end":140535162,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535162,"source":"dbSNP","seq_region_name":"7","id":"rs1334499184","clinical_significance":[]},{"end":140535167,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140535167,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1306979212","clinical_significance":[]},{"clinical_significance":[],"id":"rs1796414113","seq_region_name":"7","source":"dbSNP","start":140535168,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140535168,"alleles":["A","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1387680378","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140535175,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535175},{"alleles":["C","T"],"end":140535178,"strand":1,"feature_type":"variation","start":140535178,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs766300272","clinical_significance":[]},{"seq_region_name":"7","id":"rs1329033897","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535179,"source":"dbSNP","strand":1,"feature_type":"variation","end":140535179,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs963805543","clinical_significance":[],"alleles":["C","T"],"end":140535191,"strand":1,"feature_type":"variation","start":140535191,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1563122936","clinical_significance":[],"alleles":["CCCC","CCC"],"end":140535196,"strand":1,"feature_type":"variation","start":140535193,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs375125568","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535194,"feature_type":"variation","strand":1,"end":140535194,"alleles":["C","G"]},{"strand":1,"feature_type":"variation","end":140535195,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535195,"source":"dbSNP","seq_region_name":"7","id":"rs973479964","clinical_significance":[]},{"source":"dbSNP","start":140535199,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140535199,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796414889"},{"clinical_significance":[],"id":"rs1585570632","seq_region_name":"7","source":"dbSNP","start":140535202,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140535202,"alleles":["C","A"],"feature_type":"variation","strand":1},{"alleles":["GGAAGG","GGAAGGAAGG"],"end":140535209,"feature_type":"variation","strand":1,"source":"dbSNP","start":140535204,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796415145"},{"start":140535209,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140535209,"alleles":["G","C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs871271","clinical_significance":[]},{"seq_region_name":"7","id":"rs1355224493","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535223,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140535223},{"seq_region_name":"7","id":"rs1213740222","clinical_significance":[],"strand":1,"feature_type":"variation","end":140535225,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535225,"source":"dbSNP"},{"start":140535226,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140535226,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs1361971686","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140535228,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140535228,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1796415693","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796415795","end":140535236,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140535236,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140535237,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535237,"source":"dbSNP","seq_region_name":"7","id":"rs906308618","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130493536","clinical_significance":[],"end":140535250,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140535250,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140535251,"alleles":["T","-"],"strand":1,"feature_type":"variation","start":140535251,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1796416110","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796416281","end":140535254,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140535254,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1001907685","clinical_significance":[],"end":140535257,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140535257,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140535271,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140535271,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1033497926","seq_region_name":"7"},{"seq_region_name":"7","id":"rs912147626","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535273,"source":"dbSNP","strand":1,"feature_type":"variation","end":140535273,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1197457338","clinical_significance":[],"start":140535274,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140535274,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"end":140535290,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140535290,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796416858"},{"id":"rs1585570717","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140535294,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535294,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140535296,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535296,"clinical_significance":[],"seq_region_name":"7","id":"rs963169067"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1490246770","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140535298,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535298},{"seq_region_name":"7","id":"rs943593622","clinical_significance":[],"alleles":["C","T"],"end":140535300,"strand":1,"feature_type":"variation","start":140535300,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs774405185","source":"dbSNP","start":140535301,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140535301,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585570756","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535304,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140535304},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140535305,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535305,"clinical_significance":[],"id":"rs1348687944","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130493662","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140535309,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535309},{"seq_region_name":"7","id":"rs1796417872","clinical_significance":[],"alleles":["G","C"],"end":140535310,"strand":1,"feature_type":"variation","start":140535310,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1431712451","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535314,"source":"dbSNP","strand":1,"feature_type":"variation","end":140535314,"alleles":["C","A"]},{"alleles":["G","A"],"end":140535318,"feature_type":"variation","strand":1,"source":"dbSNP","start":140535318,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1464726436","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1224690490","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535319,"feature_type":"variation","strand":1,"end":140535319,"alleles":["T","-"]},{"start":140535322,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140535322,"strand":1,"feature_type":"variation","id":"rs1193236411","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130493699","feature_type":"variation","strand":1,"end":140535329,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535329},{"seq_region_name":"7","id":"rs1326025136","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535332,"source":"dbSNP","strand":1,"feature_type":"variation","end":140535332,"alleles":["G","A"]},{"feature_type":"variation","strand":1,"alleles":["G","A","C","T"],"end":140535339,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535339,"clinical_significance":[],"seq_region_name":"7","id":"rs1026668005"},{"alleles":["G","T"],"end":140535341,"strand":1,"feature_type":"variation","start":140535341,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs950623584","clinical_significance":[]},{"seq_region_name":"7","id":"rs1404790846","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535348,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","G"],"end":140535348},{"seq_region_name":"7","id":"rs920931081","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140535351,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535351,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130493760","source":"dbSNP","start":140535353,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140535353,"alleles":["T","C"],"feature_type":"variation","strand":1},{"start":140535356,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140535356,"alleles":["C","A"],"strand":1,"feature_type":"variation","id":"rs1381076826","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535360,"feature_type":"variation","strand":1,"end":140535360,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585570863"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535374,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140535374,"seq_region_name":"7","id":"rs555838977","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796419094","alleles":["A","G"],"end":140535376,"feature_type":"variation","strand":1,"source":"dbSNP","start":140535376,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535378,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140535378,"id":"rs1441635341","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140535379,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535379,"clinical_significance":[],"seq_region_name":"7","id":"rs1318619300"},{"id":"rs1796419368","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535383,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140535383},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535386,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140535386,"clinical_significance":[],"seq_region_name":"7","id":"rs1796419462"},{"alleles":["C","T"],"end":140535387,"strand":1,"feature_type":"variation","start":140535387,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1383382779","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535388,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140535388,"id":"rs947163606","seq_region_name":"7","clinical_significance":[]},{"start":140535389,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140535389,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1382179298","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535391,"feature_type":"variation","strand":1,"alleles":["GG","G"],"end":140535392,"clinical_significance":[],"seq_region_name":"7","id":"rs1796419846"},{"seq_region_name":"7","id":"rs1156872722","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535394,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140535394},{"seq_region_name":"7","id":"rs773322670","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140535395,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535395,"source":"dbSNP"},{"start":140535403,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140535403,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs1796420137","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535406,"feature_type":"variation","strand":1,"alleles":["A","C","T"],"end":140535406,"clinical_significance":[],"seq_region_name":"7","id":"rs1458838110"},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140535410,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535410,"clinical_significance":[],"id":"rs145434531","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1173972416","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535411,"source":"dbSNP","strand":1,"feature_type":"variation","end":140535415,"alleles":["AAAAC","-"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs189378701","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535415,"feature_type":"variation","strand":1,"end":140535415,"alleles":["C","A","T"]},{"source":"dbSNP","start":140535416,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140535416,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs975475795","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140535419,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535419,"clinical_significance":[],"seq_region_name":"7","id":"rs1439797472"},{"end":140535424,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140535424,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796421170"},{"alleles":["C","T"],"end":140535425,"strand":1,"feature_type":"variation","start":140535425,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796421257","clinical_significance":[]},{"end":140535428,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140535428,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs921459868","clinical_significance":[]},{"alleles":["C","T"],"end":140535433,"feature_type":"variation","strand":1,"source":"dbSNP","start":140535433,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796421443"},{"seq_region_name":"7","id":"rs1331617604","clinical_significance":[],"end":140535434,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140535434,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140535435,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535435,"source":"dbSNP","id":"rs554092881","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796421727","clinical_significance":[],"start":140535440,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140535440,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535441,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140535441,"clinical_significance":[],"seq_region_name":"7","id":"rs1796421811"},{"id":"rs1585571075","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140535442,"strand":1,"feature_type":"variation","start":140535442,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140535445,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535445,"source":"dbSNP","id":"rs1204790684","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796422151","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535447,"feature_type":"variation","strand":1,"end":140535447,"alleles":["C","T"]},{"feature_type":"variation","strand":1,"end":140535449,"alleles":["G","C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535449,"clinical_significance":[],"seq_region_name":"7","id":"rs936843447"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1053919594","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535453,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140535453},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535454,"feature_type":"variation","strand":1,"end":140535454,"alleles":["T","C"],"clinical_significance":[],"id":"rs1585571108","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585571112","source":"dbSNP","start":140535455,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140535455,"alleles":["C","G"],"feature_type":"variation","strand":1},{"id":"rs752469005","seq_region_name":"7","clinical_significance":[],"start":140535457,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140535457,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs147684754","seq_region_name":"7","source":"dbSNP","start":140535460,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140535460,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535461,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140535461,"seq_region_name":"7","id":"rs1023423561","clinical_significance":[]},{"end":140535471,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140535471,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1270369949","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796423053","source":"dbSNP","start":140535476,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140535476,"alleles":["G","T"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535478,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140535478,"clinical_significance":[],"seq_region_name":"7","id":"rs1229181745"},{"strand":1,"feature_type":"variation","end":140535480,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535480,"source":"dbSNP","seq_region_name":"7","id":"rs1796423237","clinical_significance":[]},{"start":140535483,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140535483,"alleles":["A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796423340","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535484,"feature_type":"variation","strand":1,"end":140535484,"alleles":["C","T"],"clinical_significance":[],"id":"rs1324105881","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1319301057","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140535487,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535487},{"id":"rs545989287","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535503,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140535503},{"alleles":["C","T"],"end":140535508,"strand":1,"feature_type":"variation","start":140535508,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs558297125","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535510,"feature_type":"variation","strand":1,"end":140535510,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs871272"},{"clinical_significance":[],"id":"rs1408181641","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535512,"feature_type":"variation","strand":1,"end":140535512,"alleles":["G","A"]},{"start":140535513,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140535513,"strand":1,"feature_type":"variation","id":"rs1263520058","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796424196","clinical_significance":[],"end":140535519,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140535519,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1334662807","feature_type":"variation","strand":1,"end":140535522,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535522},{"seq_region_name":"7","id":"rs1796424375","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535524,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140535524},{"seq_region_name":"7","id":"rs906183104","clinical_significance":[],"alleles":["T","C"],"end":140535525,"strand":1,"feature_type":"variation","start":140535525,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535529,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140535529,"seq_region_name":"7","id":"rs368332867","clinical_significance":[]},{"source":"dbSNP","start":140535530,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140535530,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1796424659","seq_region_name":"7"},{"id":"rs1198976262","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140535533,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535533,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1419993993","seq_region_name":"7","feature_type":"variation","strand":1,"end":140535534,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535534},{"seq_region_name":"7","id":"rs1169816540","clinical_significance":[],"end":140535536,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140535536,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140535538,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140535538,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1474550371"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1054816396","alleles":["G","A"],"end":140535539,"feature_type":"variation","strand":1,"source":"dbSNP","start":140535539,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1026412135","feature_type":"variation","strand":1,"end":140535542,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535542},{"seq_region_name":"7","id":"rs1796425264","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535543,"source":"dbSNP","strand":1,"feature_type":"variation","end":140535543,"alleles":["G","T"]},{"start":140535544,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140535544,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796425359","clinical_significance":[]},{"end":140535546,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140535546,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796425460","clinical_significance":[]},{"alleles":["G","A"],"end":140535547,"strand":1,"feature_type":"variation","start":140535547,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs763849563","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535551,"feature_type":"variation","strand":1,"end":140535551,"alleles":["C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs987639967"},{"strand":1,"feature_type":"variation","end":140535555,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535555,"source":"dbSNP","seq_region_name":"7","id":"rs1203620709","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796425828","clinical_significance":[],"start":140535556,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140535556,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535559,"feature_type":"variation","strand":1,"end":140535559,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1796425913"},{"seq_region_name":"7","id":"rs1585571364","clinical_significance":[],"start":140535564,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140535564,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"alleles":["G","A"],"end":140535565,"strand":1,"feature_type":"variation","start":140535565,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs181833475","clinical_significance":[]},{"seq_region_name":"7","id":"rs377047041","clinical_significance":[],"strand":1,"feature_type":"variation","end":140535566,"alleles":["C","A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535566,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1275566418","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535566,"source":"dbSNP","strand":1,"feature_type":"variation","end":140535571,"alleles":["CTTCTT","CTT"]},{"source":"dbSNP","start":140535569,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140535569,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs78434426"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535570,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140535570,"seq_region_name":"7","id":"rs76056622","clinical_significance":[]},{"seq_region_name":"7","id":"rs562088190","clinical_significance":[],"start":140535570,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140535583,"alleles":["TTTTTTTTTTTTTT","TTTTTTTTTTT","TTTTTTTTTTTT","TTTTTTTTTTTTT","TTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTT"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796426943","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535572,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140535572},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140535580,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535580,"source":"dbSNP","seq_region_name":"7","id":"rs1796427045","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140535583,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535583,"source":"dbSNP","seq_region_name":"7","id":"rs1312774339","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1407319432","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535584,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140535584},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535584,"feature_type":"variation","strand":1,"alleles":["AA","A"],"end":140535585,"clinical_significance":[],"seq_region_name":"7","id":"rs1796427289"},{"id":"rs1796427382","seq_region_name":"7","clinical_significance":[],"alleles":["AA","-"],"end":140535585,"strand":1,"feature_type":"variation","start":140535584,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1424955645","clinical_significance":[],"alleles":["A","T"],"end":140535585,"strand":1,"feature_type":"variation","start":140535585,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140535586,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TTTTTT","TTTTT","TTTTTTT"],"end":140535591,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1354829306","seq_region_name":"7"},{"start":140535591,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140535591,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1330629596","clinical_significance":[]},{"seq_region_name":"7","id":"rs1367168622","clinical_significance":[],"strand":1,"feature_type":"variation","end":140535592,"alleles":["A","C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535592,"source":"dbSNP"},{"source":"dbSNP","start":140535592,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140535593,"alleles":["AC","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1167524120"},{"seq_region_name":"7","id":"rs1796427983","clinical_significance":[],"start":140535593,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140535593,"strand":1,"feature_type":"variation"},{"id":"rs1796428089","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140535596,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535596,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140535607,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535607,"clinical_significance":[],"seq_region_name":"7","id":"rs1370158454"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1164492600","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535611,"feature_type":"variation","strand":1,"end":140535611,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs561989571","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140535612,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535612},{"source":"dbSNP","start":140535613,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140535613,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs950724570","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["TTGTTG","TTG"],"end":140535621,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535616,"source":"dbSNP","id":"rs2130494509","seq_region_name":"7","clinical_significance":[]},{"id":"rs1383483318","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535617,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140535617},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535622,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140535622,"seq_region_name":"7","id":"rs1796428633","clinical_significance":[]},{"source":"dbSNP","start":140535629,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140535629,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130494542"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140535630,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535630,"clinical_significance":[],"seq_region_name":"7","id":"rs1008812800"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535632,"feature_type":"variation","strand":1,"alleles":["AGT","-"],"end":140535634,"clinical_significance":[],"id":"rs975019679","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535633,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140535633,"clinical_significance":[],"seq_region_name":"7","id":"rs1796428923"},{"seq_region_name":"7","id":"rs1020055897","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535634,"source":"dbSNP","strand":1,"feature_type":"variation","end":140535634,"alleles":["T","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796429096","end":140535637,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140535637,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130494591","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140535641,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535641},{"id":"rs920953387","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140535642,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535642,"source":"dbSNP"},{"seq_region_name":"7","id":"rs186476604","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535643,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140535643},{"seq_region_name":"7","id":"rs1273420491","clinical_significance":[],"alleles":["C","T"],"end":140535645,"strand":1,"feature_type":"variation","start":140535645,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140535646,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535646,"source":"dbSNP","seq_region_name":"7","id":"rs975380911","clinical_significance":[]},{"end":140535647,"alleles":["T","TT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140535647,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796429539"},{"seq_region_name":"7","id":"rs753328652","clinical_significance":[],"start":140535648,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140535648,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535654,"feature_type":"variation","strand":1,"end":140535654,"alleles":["T","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs958075608"},{"clinical_significance":[],"seq_region_name":"7","id":"rs541361695","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140535657,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535657},{"seq_region_name":"7","id":"rs113046790","clinical_significance":[],"start":140535658,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140535658,"alleles":["G","A","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796430091","feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140535664,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535664},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535665,"feature_type":"variation","strand":1,"end":140535665,"alleles":["T","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1796430203"},{"seq_region_name":"7","id":"rs190863123","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535666,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140535666},{"seq_region_name":"7","id":"rs1796430437","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140535667,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535667,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1796430527","clinical_significance":[],"strand":1,"feature_type":"variation","end":140535671,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535671,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140535675,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535675,"clinical_significance":[],"seq_region_name":"7","id":"rs1796430645"},{"clinical_significance":[],"id":"rs1259714873","seq_region_name":"7","source":"dbSNP","start":140535676,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140535676,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796430829","source":"dbSNP","start":140535677,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140535677,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140535682,"alleles":["AA","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535681,"clinical_significance":[],"id":"rs1796430925","seq_region_name":"7"},{"end":140535683,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140535683,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796431032","clinical_significance":[]},{"seq_region_name":"7","id":"rs180861917","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535684,"source":"dbSNP","strand":1,"feature_type":"variation","end":140535684,"alleles":["C","T"]},{"source":"dbSNP","start":140535685,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140535685,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1585571714","seq_region_name":"7"},{"alleles":["T","G"],"end":140535688,"strand":1,"feature_type":"variation","start":140535688,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796431339","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1439709293","feature_type":"variation","strand":1,"alleles":["CTCCT","CT"],"end":140535693,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535689},{"clinical_significance":[],"id":"rs1796431540","seq_region_name":"7","end":140535693,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140535693,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140535694,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140535694,"alleles":["A","G"],"strand":1,"feature_type":"variation","id":"rs1796431633","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140535696,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535696,"source":"dbSNP","id":"rs1046632490","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs11765276","end":140535700,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140535700,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796431899","source":"dbSNP","start":140535702,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140535702,"alleles":["C","T"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535707,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140535707,"seq_region_name":"7","id":"rs928192404","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796432125","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140535710,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535710},{"seq_region_name":"7","id":"rs1796432218","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140535712,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535712,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535713,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140535713,"clinical_significance":[],"seq_region_name":"7","id":"rs1303934731"},{"start":140535716,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140535716,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796432399","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796432495","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535717,"feature_type":"variation","strand":1,"end":140535717,"alleles":["G","T"]},{"start":140535722,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140535722,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs569362103","clinical_significance":[]},{"start":140535723,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140535723,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796432677","clinical_significance":[]},{"clinical_significance":[],"id":"rs1363719018","seq_region_name":"7","feature_type":"variation","strand":1,"end":140535725,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535725},{"end":140535727,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","start":140535727,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796432848","clinical_significance":[]},{"seq_region_name":"7","id":"rs1164158488","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535728,"source":"dbSNP","strand":1,"feature_type":"variation","end":140535728,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796432983","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535729,"feature_type":"variation","strand":1,"end":140535729,"alleles":["G","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535730,"source":"dbSNP","strand":1,"feature_type":"variation","end":140535730,"alleles":["T","C"],"seq_region_name":"7","id":"rs1056904160","clinical_significance":[]},{"alleles":["C","G"],"end":140535735,"strand":1,"feature_type":"variation","start":140535735,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1410762398","seq_region_name":"7","clinical_significance":[]},{"start":140535738,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140535738,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796433259","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140535740,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535740,"clinical_significance":[],"seq_region_name":"7","id":"rs375802664"},{"start":140535751,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140535751,"strand":1,"feature_type":"variation","id":"rs895643840","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1270069807","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535754,"source":"dbSNP","strand":1,"feature_type":"variation","end":140535754,"alleles":["G","A"]},{"alleles":["A","G"],"end":140535762,"feature_type":"variation","strand":1,"source":"dbSNP","start":140535762,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs564219013"},{"strand":1,"feature_type":"variation","end":140535765,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535765,"source":"dbSNP","seq_region_name":"7","id":"rs1199612593","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535766,"source":"dbSNP","strand":1,"feature_type":"variation","end":140535766,"alleles":["C","T"],"id":"rs1490736235","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1266399728","end":140535767,"alleles":["A","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140535767,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140535771,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535771,"clinical_significance":[],"seq_region_name":"7","id":"rs1585571877"},{"end":140535773,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140535773,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796433947","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535774,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140535774,"seq_region_name":"7","id":"rs2130494996","clinical_significance":[]},{"start":140535775,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140535775,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs898925884","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1183618029","source":"dbSNP","start":140535779,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140535779,"alleles":["A","C","G"],"feature_type":"variation","strand":1},{"end":140535782,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140535782,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796434271"},{"alleles":["T","A"],"end":140535786,"feature_type":"variation","strand":1,"source":"dbSNP","start":140535786,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796434359"},{"clinical_significance":[],"id":"rs1796434454","seq_region_name":"7","source":"dbSNP","start":140535788,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140535788,"alleles":["G","A"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140535797,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140535797,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796434543"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796434643","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535800,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140535800},{"end":140535803,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140535803,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1796434738","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1585571914","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535804,"feature_type":"variation","strand":1,"end":140535804,"alleles":["A","C"]},{"seq_region_name":"7","id":"rs1585571925","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535805,"source":"dbSNP","strand":1,"feature_type":"variation","end":140535805,"alleles":["C","T"]},{"strand":1,"feature_type":"variation","end":140535808,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535808,"source":"dbSNP","id":"rs1796435015","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1286209589","source":"dbSNP","start":140535810,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["GACTTCAGA","GA"],"end":140535818,"feature_type":"variation","strand":1},{"alleles":["T","C"],"end":140535814,"strand":1,"feature_type":"variation","start":140535814,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs994535604","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796435304","clinical_significance":[],"strand":1,"feature_type":"variation","end":140535817,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535817,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1328154562","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140535821,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535821},{"source":"dbSNP","start":140535825,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140535825,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1585571975","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1796435587","clinical_significance":[],"start":140535831,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140535831,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"end":140535833,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140535833,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1048060674","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs539976674","source":"dbSNP","start":140535834,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140535834,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796435839","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140535835,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535835},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535836,"source":"dbSNP","strand":1,"feature_type":"variation","end":140535836,"alleles":["C","A"],"seq_region_name":"7","id":"rs948686901","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535837,"source":"dbSNP","strand":1,"feature_type":"variation","end":140535837,"alleles":["C","A"],"seq_region_name":"7","id":"rs1293201159","clinical_significance":[]},{"end":140535842,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140535842,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1796436133","seq_region_name":"7","clinical_significance":[]},{"start":140535846,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140535846,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796436238","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535850,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140535850,"clinical_significance":[],"seq_region_name":"7","id":"rs1796436333"},{"end":140535852,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140535852,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1431522831","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1426207784","clinical_significance":[],"end":140535856,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140535856,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1585572030","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535857,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140535857},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796436609","source":"dbSNP","start":140535859,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140535859,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535865,"source":"dbSNP","strand":1,"feature_type":"variation","end":140535865,"alleles":["A","G"],"seq_region_name":"7","id":"rs886254547","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796436812","feature_type":"variation","strand":1,"end":140535866,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535866},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535872,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140535872,"seq_region_name":"7","id":"rs776969878","clinical_significance":[]},{"clinical_significance":[],"id":"rs1563123290","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140535873,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535873},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535876,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140535876,"seq_region_name":"7","id":"rs1009257193","clinical_significance":[]},{"start":140535878,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140535878,"alleles":["G","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs899046428","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1018874868","source":"dbSNP","start":140535879,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140535879,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140535880,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140535880,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1179011497","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1463789702","alleles":["C","T"],"end":140535881,"feature_type":"variation","strand":1,"source":"dbSNP","start":140535881,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs531351581","clinical_significance":[],"start":140535882,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140535882,"alleles":["G","A","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1796437975","clinical_significance":[],"start":140535889,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140535889,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs562281906","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535892,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140535892},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535896,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140535896,"seq_region_name":"7","id":"rs1585572147","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535905,"source":"dbSNP","strand":1,"feature_type":"variation","end":140535905,"alleles":["A","C"],"seq_region_name":"7","id":"rs1796438459","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs551809738","source":"dbSNP","start":140535908,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140535908,"alleles":["C","A","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs549838290","clinical_significance":[],"start":140535909,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140535909,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1796438918","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140535910,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535910,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140535911,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535911,"source":"dbSNP","seq_region_name":"7","id":"rs886529675","clinical_significance":[]},{"source":"dbSNP","start":140535915,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140535915,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1263733441","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs567998268","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535916,"feature_type":"variation","strand":1,"end":140535916,"alleles":["C","T"]},{"end":140535917,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140535917,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1300522125","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140535918,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140535918,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796439647"},{"seq_region_name":"7","id":"rs1354786577","clinical_significance":[],"start":140535919,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140535919,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535926,"feature_type":"variation","strand":1,"end":140535926,"alleles":["G","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs535419554"},{"seq_region_name":"7","id":"rs1300792393","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140535929,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535929,"source":"dbSNP"},{"alleles":["C","T"],"end":140535935,"strand":1,"feature_type":"variation","start":140535935,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1796440378","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535937,"feature_type":"variation","strand":1,"end":140535937,"alleles":["A","C","G"],"clinical_significance":[],"id":"rs2130495432","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1796440491","clinical_significance":[],"strand":1,"feature_type":"variation","end":140535943,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535943,"source":"dbSNP"},{"source":"dbSNP","start":140535944,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140535944,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1215398656"},{"feature_type":"variation","strand":1,"end":140535946,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535946,"clinical_significance":[],"seq_region_name":"7","id":"rs1796440752"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796440909","alleles":["A","C","T"],"end":140535950,"feature_type":"variation","strand":1,"source":"dbSNP","start":140535950,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1364092307","source":"dbSNP","start":140535951,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140535951,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1434535220","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535955,"feature_type":"variation","strand":1,"end":140535955,"alleles":["C","G"]},{"end":140535956,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140535956,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1407445507","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535956,"feature_type":"variation","strand":1,"end":140535959,"alleles":["TTTT","TTTTT"],"clinical_significance":[],"seq_region_name":"7","id":"rs1287190617"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563123351","alleles":["T","C"],"end":140535957,"feature_type":"variation","strand":1,"source":"dbSNP","start":140535957,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140535959,"alleles":["T","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535959,"source":"dbSNP","seq_region_name":"7","id":"rs1279920638","clinical_significance":[]},{"alleles":["T","C"],"end":140535961,"strand":1,"feature_type":"variation","start":140535961,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796441896","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140535969,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535969,"clinical_significance":[],"id":"rs1796442034","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs577297855","alleles":["C","T"],"end":140535971,"feature_type":"variation","strand":1,"source":"dbSNP","start":140535971,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140535972,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535972,"source":"dbSNP","id":"rs1377444908","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796442377","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535975,"source":"dbSNP","strand":1,"feature_type":"variation","end":140535975,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs958147737","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140535979,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535979,"source":"dbSNP"},{"alleles":["G","A"],"end":140535980,"feature_type":"variation","strand":1,"source":"dbSNP","start":140535980,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs975430097"},{"alleles":["G","A","T"],"end":140535984,"strand":1,"feature_type":"variation","start":140535984,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1312944189","clinical_significance":[]},{"source":"dbSNP","start":140535985,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140535985,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs758658313","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1186098851","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535986,"feature_type":"variation","strand":1,"end":140535986,"alleles":["T","A"]},{"clinical_significance":[],"id":"rs547733574","seq_region_name":"7","feature_type":"variation","strand":1,"end":140535989,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535989},{"clinical_significance":[],"id":"rs186522233","seq_region_name":"7","alleles":["A","T"],"end":140535990,"feature_type":"variation","strand":1,"source":"dbSNP","start":140535990,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1796443222","clinical_significance":[],"strand":1,"feature_type":"variation","end":140535991,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140535991,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796443319","feature_type":"variation","strand":1,"alleles":["A","-"],"end":140535992,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535992},{"id":"rs2130495615","seq_region_name":"7","clinical_significance":[],"start":140535993,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140535993,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"alleles":["A","C"],"end":140535995,"strand":1,"feature_type":"variation","start":140535995,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1243639564","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140535996,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140535996,"clinical_significance":[],"seq_region_name":"7","id":"rs989564045"},{"source":"dbSNP","start":140536004,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140536004,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1205508593"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585572412","source":"dbSNP","start":140536005,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140536005,"feature_type":"variation","strand":1},{"end":140536008,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140536008,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1021571361","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140536009,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536009,"clinical_significance":[],"seq_region_name":"7","id":"rs77471923"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796444022","feature_type":"variation","strand":1,"end":140536010,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536010},{"id":"rs934446928","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140536012,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536012,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1796444204","clinical_significance":[],"start":140536017,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140536017,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796444285","feature_type":"variation","strand":1,"end":140536018,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536018},{"source":"dbSNP","start":140536020,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140536020,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1796444381","seq_region_name":"7"},{"end":140536027,"alleles":["AGA","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140536025,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796444471"},{"seq_region_name":"7","id":"rs2130495739","clinical_significance":[],"start":140536029,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140536029,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585572449","alleles":["G","C"],"end":140536034,"feature_type":"variation","strand":1,"source":"dbSNP","start":140536034,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536043,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140536043,"clinical_significance":[],"seq_region_name":"7","id":"rs1796444647"},{"seq_region_name":"7","id":"rs1796444738","clinical_significance":[],"strand":1,"feature_type":"variation","end":140536046,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536046,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536046,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CACTCACT","CACT"],"end":140536053,"id":"rs1796444824","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","G"],"end":140536047,"feature_type":"variation","strand":1,"source":"dbSNP","start":140536047,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs992589636"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536050,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140536050,"clinical_significance":[],"seq_region_name":"7","id":"rs1227714898"},{"seq_region_name":"7","id":"rs982666262","clinical_significance":[],"start":140536051,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140536051,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs2130495804","clinical_significance":[],"alleles":["A","T"],"end":140536057,"strand":1,"feature_type":"variation","start":140536057,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1383657478","seq_region_name":"7","end":140536059,"alleles":["AAA","AA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140536057,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs928220349","alleles":["T","C"],"end":140536064,"feature_type":"variation","strand":1,"source":"dbSNP","start":140536064,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536068,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140536068,"seq_region_name":"7","id":"rs1265885461","clinical_significance":[]},{"alleles":["A","T"],"end":140536069,"strand":1,"feature_type":"variation","start":140536069,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1317715088","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs557619050","end":140536070,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140536070,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140536072,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536072,"source":"dbSNP","seq_region_name":"7","id":"rs1796445691","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585572550","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536073,"source":"dbSNP","strand":1,"feature_type":"variation","end":140536073,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1585572558","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140536074,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536074,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1451111688","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536075,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140536075},{"seq_region_name":"7","id":"rs1796446100","clinical_significance":[],"alleles":["G","C"],"end":140536076,"strand":1,"feature_type":"variation","start":140536076,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs917096572","seq_region_name":"7","clinical_significance":[],"alleles":["G","C","T"],"end":140536077,"strand":1,"feature_type":"variation","start":140536077,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs191352310","source":"dbSNP","start":140536079,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140536079,"alleles":["A","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs2130495913","clinical_significance":[],"strand":1,"feature_type":"variation","end":140536080,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536080,"source":"dbSNP"},{"id":"rs1796446443","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140536084,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536084,"source":"dbSNP"},{"seq_region_name":"7","id":"rs537190919","clinical_significance":[],"start":140536085,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140536085,"alleles":["G","A","T"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140536090,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536090,"source":"dbSNP","seq_region_name":"7","id":"rs555816953","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536091,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140536091,"clinical_significance":[],"seq_region_name":"7","id":"rs573728634"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140536092,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536092,"source":"dbSNP","seq_region_name":"7","id":"rs1415787551","clinical_significance":[]},{"start":140536100,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140536100,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796446830","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536101,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140536101,"clinical_significance":[],"id":"rs1796446912","seq_region_name":"7"},{"alleles":["A","G"],"end":140536104,"feature_type":"variation","strand":1,"source":"dbSNP","start":140536104,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585572670"},{"source":"dbSNP","start":140536107,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A","C","G"],"end":140536107,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1047793722"},{"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140536108,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536108,"source":"dbSNP","seq_region_name":"7","id":"rs1796447239","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140536112,"alleles":["G","GCG"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536112,"source":"dbSNP","seq_region_name":"7","id":"rs1796447327","clinical_significance":[]},{"clinical_significance":[],"id":"rs1385328827","seq_region_name":"7","source":"dbSNP","start":140536116,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140536116,"alleles":["G","C"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140536117,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536117,"clinical_significance":[],"seq_region_name":"7","id":"rs1185276620"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536118,"source":"dbSNP","strand":1,"feature_type":"variation","end":140536118,"alleles":["T","G"],"id":"rs930412727","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140536121,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536121,"clinical_significance":[],"id":"rs1047460389","seq_region_name":"7"},{"id":"rs373496495","seq_region_name":"7","clinical_significance":[],"start":140536123,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140536123,"alleles":["C","A","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs567188328","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536124,"feature_type":"variation","strand":1,"end":140536124,"alleles":["G","A"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536125,"feature_type":"variation","strand":1,"end":140536125,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130496048"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1019015423","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536129,"feature_type":"variation","strand":1,"end":140536129,"alleles":["G","A","C"]},{"seq_region_name":"7","id":"rs375957286","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140536140,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536140,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1796448237","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536143,"feature_type":"variation","strand":1,"end":140536143,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs1796448331","clinical_significance":[],"start":140536153,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140536153,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1429799772","clinical_significance":[],"strand":1,"feature_type":"variation","end":140536156,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536156,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140536157,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536157,"clinical_significance":[],"seq_region_name":"7","id":"rs1796448527"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1275179383","source":"dbSNP","start":140536158,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140536158,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs59191670","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536163,"source":"dbSNP","strand":1,"feature_type":"variation","end":140536163,"alleles":["G","A"]},{"start":140536165,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140536165,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796448793","clinical_significance":[]},{"end":140536167,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140536167,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1796448873","seq_region_name":"7","clinical_significance":[]},{"id":"rs1796448961","seq_region_name":"7","clinical_significance":[],"start":140536169,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140536169,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs900455215","clinical_significance":[],"strand":1,"feature_type":"variation","end":140536170,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536170,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs58821916","source":"dbSNP","start":140536171,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140536171,"alleles":["A","G"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140536173,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536173,"clinical_significance":[],"seq_region_name":"7","id":"rs1221137939"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536175,"feature_type":"variation","strand":1,"alleles":["AAA","AA"],"end":140536177,"clinical_significance":[],"id":"rs550459576","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1796449415","clinical_significance":[],"start":140536177,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140536177,"alleles":["A","C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1347240604","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140536181,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536181,"source":"dbSNP"},{"end":140536182,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140536182,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1217351811"},{"clinical_significance":[],"id":"rs996091911","seq_region_name":"7","source":"dbSNP","start":140536185,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140536185,"alleles":["T","G"],"feature_type":"variation","strand":1},{"start":140536188,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140536188,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796449866","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140536189,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536189,"source":"dbSNP","seq_region_name":"7","id":"rs1288806473","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536197,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140536197,"seq_region_name":"7","id":"rs1308389045","clinical_significance":[]},{"id":"rs1796450140","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536201,"source":"dbSNP","strand":1,"feature_type":"variation","end":140536201,"alleles":["A","G"]},{"start":140536204,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140536204,"alleles":["A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs968283030","clinical_significance":[]},{"seq_region_name":"7","id":"rs1028354072","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536206,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140536206},{"alleles":["A","G"],"end":140536212,"strand":1,"feature_type":"variation","start":140536212,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs182841050","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1011296864","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140536215,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536215},{"clinical_significance":[],"id":"rs577877172","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140536216,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536216},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796450739","source":"dbSNP","start":140536218,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140536232,"alleles":["GGTGGCACATGCCTA","-"],"feature_type":"variation","strand":1},{"end":140536219,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140536219,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs978298993","clinical_significance":[]},{"seq_region_name":"7","id":"rs143317334","clinical_significance":[],"strand":1,"feature_type":"variation","end":140536226,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536226,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796451025","alleles":["A","AA"],"end":140536226,"feature_type":"variation","strand":1,"source":"dbSNP","start":140536226,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140536229,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140536229,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1796451103","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796451196","source":"dbSNP","start":140536230,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140536230,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130496349","end":140536232,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140536232,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536233,"feature_type":"variation","strand":1,"end":140536233,"alleles":["T","C"],"clinical_significance":[],"id":"rs1796451270","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1478838769","clinical_significance":[],"start":140536234,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","AA"],"end":140536234,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140536241,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140536241,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1191353222"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536244,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140536244,"clinical_significance":[],"seq_region_name":"7","id":"rs1585572945"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140536260,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536260,"source":"dbSNP","seq_region_name":"7","id":"rs373355358","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140536265,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536265,"clinical_significance":[],"seq_region_name":"7","id":"rs1796451705"},{"alleles":["A","G"],"end":140536266,"feature_type":"variation","strand":1,"source":"dbSNP","start":140536266,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs982309064"},{"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140536267,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536267,"clinical_significance":[],"id":"rs1796451860","seq_region_name":"7"},{"end":140536269,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140536269,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs563769773","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","G"],"end":140536275,"strand":1,"feature_type":"variation","start":140536275,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1796452078","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140536278,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536278,"source":"dbSNP","id":"rs1796452162","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536279,"feature_type":"variation","strand":1,"end":140536279,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1796452243"},{"seq_region_name":"7","id":"rs531117552","clinical_significance":[],"start":140536282,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140536282,"alleles":["G","A","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796452461","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536285,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140536285},{"id":"rs955701968","seq_region_name":"7","clinical_significance":[],"end":140536286,"alleles":["T","A","G"],"strand":1,"feature_type":"variation","start":140536286,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs549639090","end":140536291,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140536291,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536292,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140536292,"seq_region_name":"7","id":"rs1585573011","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585573026","feature_type":"variation","strand":1,"end":140536294,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536294},{"feature_type":"variation","strand":1,"end":140536295,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536295,"clinical_significance":[],"id":"rs1796452875","seq_region_name":"7"},{"id":"rs1035141287","seq_region_name":"7","clinical_significance":[],"start":140536298,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C","G"],"end":140536298,"strand":1,"feature_type":"variation"},{"alleles":["G","A"],"end":140536299,"feature_type":"variation","strand":1,"source":"dbSNP","start":140536299,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1796453095","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536303,"feature_type":"variation","strand":1,"end":140536303,"alleles":["C","G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1420601902"},{"clinical_significance":[],"id":"rs561791804","seq_region_name":"7","feature_type":"variation","strand":1,"end":140536304,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536304},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536308,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140536308,"clinical_significance":[],"seq_region_name":"7","id":"rs1796453391"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796453488","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536309,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140536309},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140536313,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536313,"clinical_significance":[],"seq_region_name":"7","id":"rs991013302"},{"alleles":["C","G","T"],"end":140536316,"feature_type":"variation","strand":1,"source":"dbSNP","start":140536316,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1271392766"},{"seq_region_name":"7","id":"rs920289324","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536318,"source":"dbSNP","strand":1,"feature_type":"variation","end":140536318,"alleles":["G","T"]},{"seq_region_name":"7","id":"rs1796453807","clinical_significance":[],"start":140536319,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140536319,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"alleles":["C","-"],"end":140536319,"feature_type":"variation","strand":1,"source":"dbSNP","start":140536319,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs2130496571","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585573118","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536322,"feature_type":"variation","strand":1,"end":140536322,"alleles":["T","C"]},{"end":140536323,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140536323,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1261777005","clinical_significance":[]},{"start":140536324,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140536324,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs1585573144","seq_region_name":"7","clinical_significance":[]},{"end":140536326,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140536326,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796454184","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1241827110","end":140536327,"alleles":["C","A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140536327,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140536331,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536331,"source":"dbSNP","seq_region_name":"7","id":"rs1327437191","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1324026028","end":140536332,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140536332,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796454571","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140536335,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536335},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140536338,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536338,"clinical_significance":[],"id":"rs1585573190","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["G","GTG"],"end":140536344,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536344,"source":"dbSNP","seq_region_name":"7","id":"rs1288115565","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796454832","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140536352,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536352,"source":"dbSNP"},{"id":"rs1796454925","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140536355,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536355,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536356,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GG","GGG"],"end":140536357,"seq_region_name":"7","id":"rs1796455015","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140536357,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536357,"source":"dbSNP","seq_region_name":"7","id":"rs1405999815","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536358,"source":"dbSNP","strand":1,"feature_type":"variation","end":140536358,"alleles":["A","G"],"seq_region_name":"7","id":"rs1389413348","clinical_significance":[]},{"clinical_significance":[],"id":"rs781061820","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536358,"feature_type":"variation","strand":1,"end":140536370,"alleles":["AAAAAAAAAAAAA","AAAAAAAAAAA","AAAAAAAAAAAA","AAAAAAAAAAAAAA","AAAAAAAAAAAAAAA"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536361,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140536361,"id":"rs1796455484","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs979975062","alleles":["A","C"],"end":140536363,"feature_type":"variation","strand":1,"source":"dbSNP","start":140536363,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs920414779","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["AAAGAA","AA"],"end":140536373,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536368,"source":"dbSNP"},{"id":"rs1409750617","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140536370,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536370,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536371,"source":"dbSNP","strand":1,"feature_type":"variation","end":140536371,"alleles":["G","A","T"],"seq_region_name":"7","id":"rs1796455867","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536378,"feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140536378,"clinical_significance":[],"seq_region_name":"7","id":"rs375883619"},{"start":140536381,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140536381,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796456093","clinical_significance":[]},{"id":"rs151302818","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536386,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140536386},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536387,"feature_type":"variation","strand":1,"end":140536387,"alleles":["T","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585573302"},{"seq_region_name":"7","id":"rs1796456372","clinical_significance":[],"start":140536392,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140536392,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1796456472","clinical_significance":[],"alleles":["G","C"],"end":140536396,"strand":1,"feature_type":"variation","start":140536396,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536398,"feature_type":"variation","strand":1,"end":140536398,"alleles":["T","G"],"clinical_significance":[],"id":"rs1585573312","seq_region_name":"7"},{"end":140536403,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140536403,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1585573318","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796456742","end":140536408,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140536408,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["T","C","G"],"end":140536409,"strand":1,"feature_type":"variation","start":140536409,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs983497430","clinical_significance":[]},{"alleles":["C","G","T"],"end":140536411,"feature_type":"variation","strand":1,"source":"dbSNP","start":140536411,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585573333"},{"strand":1,"feature_type":"variation","end":140536412,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536412,"source":"dbSNP","seq_region_name":"7","id":"rs1796457074","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1197054203","source":"dbSNP","start":140536414,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","-"],"end":140536414,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1451052174","clinical_significance":[],"start":140536414,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C","G"],"end":140536414,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140536420,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536420,"clinical_significance":[],"id":"rs907625619","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1796457631","clinical_significance":[],"strand":1,"feature_type":"variation","end":140536421,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536421,"source":"dbSNP"},{"source":"dbSNP","start":140536421,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AAAAGGTGAA","AAAAGGTGAAAAGGTGAA"],"end":140536430,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1324143645"},{"start":140536422,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140536422,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130496896","clinical_significance":[]},{"clinical_significance":[],"id":"rs1796457796","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140536425,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536425},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536427,"feature_type":"variation","strand":1,"end":140536427,"alleles":["T","G"],"clinical_significance":[],"id":"rs1585573382","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140536429,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536429,"clinical_significance":[],"seq_region_name":"7","id":"rs1796457995"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536431,"feature_type":"variation","strand":1,"end":140536431,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1241001569"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1370459954","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536431,"feature_type":"variation","strand":1,"end":140536435,"alleles":["GATGA","GA"]},{"end":140536433,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140536433,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1796458457","seq_region_name":"7"},{"id":"rs1563123597","seq_region_name":"7","clinical_significance":[],"end":140536435,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140536435,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140536436,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140536436,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs547374477","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140536450,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536450,"source":"dbSNP","seq_region_name":"7","id":"rs565981894","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs900602751","feature_type":"variation","strand":1,"end":140536452,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536452},{"feature_type":"variation","strand":1,"end":140536454,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536454,"clinical_significance":[],"id":"rs1796459198","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796459282","feature_type":"variation","strand":1,"end":140536466,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536466},{"source":"dbSNP","start":140536468,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140536468,"alleles":["A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs996634607"},{"id":"rs1223702088","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140536471,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536471,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1043928171","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536472,"feature_type":"variation","strand":1,"end":140536472,"alleles":["G","A"]},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140536474,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536474,"clinical_significance":[],"seq_region_name":"7","id":"rs1796460026"},{"start":140536479,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140536479,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796460100","clinical_significance":[]},{"start":140536482,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140536482,"strand":1,"feature_type":"variation","id":"rs1796460185","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536485,"source":"dbSNP","strand":1,"feature_type":"variation","end":140536485,"alleles":["G","A"],"id":"rs1796460292","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140536489,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140536489,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796460382"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140536509,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536509,"clinical_significance":[],"seq_region_name":"7","id":"rs904010291"},{"seq_region_name":"7","id":"rs140601792","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140536512,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536512,"source":"dbSNP"},{"clinical_significance":[],"id":"rs900319324","seq_region_name":"7","alleles":["T","C"],"end":140536515,"feature_type":"variation","strand":1,"source":"dbSNP","start":140536515,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","A","T"],"end":140536518,"feature_type":"variation","strand":1,"source":"dbSNP","start":140536518,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1031203112","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1796460993","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536519,"source":"dbSNP","strand":1,"feature_type":"variation","end":140536519,"alleles":["A","G"]},{"id":"rs1212146289","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536520,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140536520},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796461284","source":"dbSNP","start":140536522,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140536522,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs551646403","feature_type":"variation","strand":1,"alleles":["A","T"],"end":140536523,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536523},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536524,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140536524,"clinical_significance":[],"seq_region_name":"7","id":"rs960908955"},{"seq_region_name":"7","id":"rs1252016129","clinical_significance":[],"strand":1,"feature_type":"variation","end":140536525,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536525,"source":"dbSNP"},{"source":"dbSNP","start":140536528,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140536528,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796461864"},{"id":"rs753195070","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536530,"source":"dbSNP","strand":1,"feature_type":"variation","end":140536530,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1796462038","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536532,"source":"dbSNP","strand":1,"feature_type":"variation","end":140536532,"alleles":["G","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536545,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140536545,"clinical_significance":[],"seq_region_name":"7","id":"rs1796462120"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536551,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140536551,"clinical_significance":[],"id":"rs1796462211","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796462293","source":"dbSNP","start":140536552,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140536552,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536553,"source":"dbSNP","strand":1,"feature_type":"variation","end":140536553,"alleles":["G","C"],"seq_region_name":"7","id":"rs1796462405","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536554,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140536554,"clinical_significance":[],"seq_region_name":"7","id":"rs1319853494"},{"seq_region_name":"7","id":"rs1796462537","clinical_significance":[],"end":140536556,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140536556,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536558,"source":"dbSNP","strand":1,"feature_type":"variation","end":140536558,"alleles":["T","C"],"seq_region_name":"7","id":"rs774128456","clinical_significance":[]},{"clinical_significance":[],"id":"rs552595518","seq_region_name":"7","end":140536559,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140536559,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["T","C"],"end":140536560,"strand":1,"feature_type":"variation","start":140536560,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1024363953","clinical_significance":[]},{"id":"rs1796462930","seq_region_name":"7","clinical_significance":[],"start":140536561,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140536561,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140536563,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140536563,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs2130497227","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["CTCT","CT"],"end":140536570,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536567,"clinical_significance":[],"seq_region_name":"7","id":"rs1796463033"},{"strand":1,"feature_type":"variation","end":140536568,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536568,"source":"dbSNP","seq_region_name":"7","id":"rs1796463133","clinical_significance":[]},{"clinical_significance":[],"id":"rs1054388945","seq_region_name":"7","alleles":["C","A"],"end":140536569,"feature_type":"variation","strand":1,"source":"dbSNP","start":140536569,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536574,"feature_type":"variation","strand":1,"end":140536574,"alleles":["T","-"],"clinical_significance":[],"seq_region_name":"7","id":"rs368469269"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536577,"source":"dbSNP","strand":1,"feature_type":"variation","end":140536577,"alleles":["T","G"],"seq_region_name":"7","id":"rs893022302","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536578,"source":"dbSNP","strand":1,"feature_type":"variation","end":140536578,"alleles":["G","C"],"seq_region_name":"7","id":"rs1796463516","clinical_significance":[]},{"id":"rs1796463623","seq_region_name":"7","clinical_significance":[],"end":140536579,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140536579,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796463708","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536586,"feature_type":"variation","strand":1,"end":140536586,"alleles":["T","C","G"]},{"end":140536592,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140536592,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs951852175","clinical_significance":[]},{"end":140536593,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140536593,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1415794324","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","G"],"end":140536596,"strand":1,"feature_type":"variation","start":140536596,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1459693801","clinical_significance":[]},{"seq_region_name":"7","id":"rs1163888671","clinical_significance":[],"end":140536598,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140536598,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140536599,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140536599,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1247910160","seq_region_name":"7"},{"seq_region_name":"7","id":"rs2130497353","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140536601,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536601,"source":"dbSNP"},{"id":"rs1394074161","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140536604,"alleles":["GTTC","GTTCGTTC"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536601,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140536605,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536605,"source":"dbSNP","id":"rs1010910810","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796464375","clinical_significance":[],"strand":1,"feature_type":"variation","end":140536606,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536606,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1276949780","clinical_significance":[],"start":140536619,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140536619,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796464474","source":"dbSNP","start":140536623,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140536623,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536634,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140536634,"clinical_significance":[],"id":"rs1563123681","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["TTT","TTTT"],"end":140536638,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536636,"source":"dbSNP","seq_region_name":"7","id":"rs1796464646","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796464761","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536638,"source":"dbSNP","strand":1,"feature_type":"variation","end":140536638,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1333510065","feature_type":"variation","strand":1,"alleles":["A","T"],"end":140536640,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536640},{"id":"rs1334051835","seq_region_name":"7","clinical_significance":[],"alleles":["T","G"],"end":140536641,"strand":1,"feature_type":"variation","start":140536641,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140536644,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536644,"clinical_significance":[],"id":"rs1042745951","seq_region_name":"7"},{"source":"dbSNP","start":140536650,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140536650,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs902629173"},{"strand":1,"feature_type":"variation","alleles":["AA","AAA"],"end":140536653,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536652,"source":"dbSNP","seq_region_name":"7","id":"rs1270460088","clinical_significance":[]},{"id":"rs1796465351","seq_region_name":"7","clinical_significance":[],"alleles":["AATTATACTATTAAAATT","AATT"],"end":140536669,"strand":1,"feature_type":"variation","start":140536652,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536654,"feature_type":"variation","strand":1,"end":140536654,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs907796232"},{"source":"dbSNP","start":140536660,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140536660,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs569787110"},{"source":"dbSNP","start":140536666,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140536666,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1796465792","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1285315141","clinical_significance":[],"end":140536670,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140536670,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140536671,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536671,"clinical_significance":[],"seq_region_name":"7","id":"rs1296709292"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1040388314","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536672,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140536672},{"id":"rs527666852","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["TTTTTTTTTT","TTTTTTTTT","TTTTTTTTTTT","TTTTTTTTTTTT"],"end":140536682,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536673,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563123718","alleles":["T","A"],"end":140536674,"feature_type":"variation","strand":1,"source":"dbSNP","start":140536674,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs909434982","end":140536675,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140536675,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["G","T"],"end":140536683,"feature_type":"variation","strand":1,"source":"dbSNP","start":140536683,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1397449204"},{"clinical_significance":[],"id":"rs1796466669","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536686,"feature_type":"variation","strand":1,"end":140536686,"alleles":["A","G"]},{"clinical_significance":[],"id":"rs1170755358","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536688,"feature_type":"variation","strand":1,"end":140536688,"alleles":["G","A"]},{"clinical_significance":[],"id":"rs1796466871","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140536694,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536694},{"clinical_significance":[],"seq_region_name":"7","id":"rs921913825","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536698,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140536698},{"end":140536701,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140536701,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585573893","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796467116","clinical_significance":[],"start":140536702,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140536702,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140536705,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536705,"clinical_significance":[],"id":"rs1389642350","seq_region_name":"7"},{"source":"dbSNP","start":140536706,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140536706,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1184675152","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130497643","source":"dbSNP","start":140536708,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140536708,"alleles":["A","C"],"feature_type":"variation","strand":1},{"start":140536709,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140536709,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs187480292","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536714,"feature_type":"variation","strand":1,"end":140536714,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1796467562"},{"seq_region_name":"7","id":"rs1272912852","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536716,"source":"dbSNP","strand":1,"feature_type":"variation","end":140536716,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1318215995","source":"dbSNP","start":140536719,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140536719,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs555602900","clinical_significance":[],"end":140536720,"alleles":["A","G","T"],"strand":1,"feature_type":"variation","start":140536720,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140536723,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536723,"clinical_significance":[],"id":"rs1273219801","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140536724,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536724,"source":"dbSNP","seq_region_name":"7","id":"rs34127793","clinical_significance":[]},{"end":140536727,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140536727,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796468231"},{"seq_region_name":"7","id":"rs190596549","clinical_significance":[],"start":140536736,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140536736,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1796468460","clinical_significance":[],"end":140536739,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140536739,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140536740,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140536740,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1246151628"},{"seq_region_name":"7","id":"rs1796468648","clinical_significance":[],"alleles":["C","A","T"],"end":140536746,"strand":1,"feature_type":"variation","start":140536746,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140536749,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536749,"source":"dbSNP","seq_region_name":"7","id":"rs999654157","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796468862","clinical_significance":[],"start":140536750,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140536750,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"id":"rs1052531060","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536751,"source":"dbSNP","strand":1,"feature_type":"variation","end":140536751,"alleles":["C","A","T"]},{"start":140536755,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140536755,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs896750392","clinical_significance":[]},{"start":140536757,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140536757,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1336156348","clinical_significance":[]},{"id":"rs183114695","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140536758,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536758,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536759,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140536759,"seq_region_name":"7","id":"rs577603807","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536761,"feature_type":"variation","strand":1,"end":140536761,"alleles":["C","T"],"clinical_significance":[],"id":"rs1310022194","seq_region_name":"7"},{"start":140536764,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140536764,"alleles":["G","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1408233008","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs535184037","source":"dbSNP","start":140536768,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140536768,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs545410316","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140536769,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536769},{"clinical_significance":[],"seq_region_name":"7","id":"rs557609537","alleles":["T","A"],"end":140536771,"feature_type":"variation","strand":1,"source":"dbSNP","start":140536771,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140536772,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140536772,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796469957"},{"source":"dbSNP","start":140536773,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140536773,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1014242528"},{"start":140536774,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140536774,"strand":1,"feature_type":"variation","id":"rs575770375","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1164277284","clinical_significance":[],"start":140536775,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140536775,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536777,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CTCA","CTCACTCA"],"end":140536780,"id":"rs1407201032","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563123820","end":140536781,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140536781,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1796470481","clinical_significance":[],"end":140536782,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140536782,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796470584","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536785,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140536785},{"source":"dbSNP","start":140536787,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140536787,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796470680"},{"seq_region_name":"7","id":"rs1187573464","clinical_significance":[],"start":140536788,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140536788,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1796470866","clinical_significance":[],"alleles":["T","C"],"end":140536791,"strand":1,"feature_type":"variation","start":140536791,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536794,"feature_type":"variation","strand":1,"end":140536794,"alleles":["C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1239162586"},{"id":"rs1796471081","seq_region_name":"7","clinical_significance":[],"start":140536799,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140536799,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536800,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140536800,"clinical_significance":[],"seq_region_name":"7","id":"rs952355504"},{"end":140536807,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140536807,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs543169082","seq_region_name":"7","clinical_significance":[]},{"id":"rs907531049","seq_region_name":"7","clinical_significance":[],"start":140536808,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140536808,"alleles":["G","A","C"],"strand":1,"feature_type":"variation"},{"end":140536809,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140536809,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1234967558","clinical_significance":[]},{"source":"dbSNP","start":140536810,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140536810,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796471712"},{"strand":1,"feature_type":"variation","end":140536814,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536814,"source":"dbSNP","id":"rs1180558307","seq_region_name":"7","clinical_significance":[]},{"end":140536815,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140536815,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1481862347"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536816,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140536816,"seq_region_name":"7","id":"rs1796471987","clinical_significance":[]},{"alleles":["C","T"],"end":140536821,"strand":1,"feature_type":"variation","start":140536821,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1250681699","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1222548349","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140536823,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536823},{"clinical_significance":[],"seq_region_name":"7","id":"rs1323036193","source":"dbSNP","start":140536825,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140536825,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796472336","end":140536827,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140536827,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1424052029","clinical_significance":[],"start":140536830,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140536834,"alleles":["TTTTT","TTT"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs556968854","clinical_significance":[],"alleles":["T","A"],"end":140536839,"strand":1,"feature_type":"variation","start":140536839,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1287588459","end":140536845,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140536845,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536847,"source":"dbSNP","strand":1,"feature_type":"variation","end":140536847,"alleles":["C","G"],"seq_region_name":"7","id":"rs1585574263","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1227682129","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536849,"feature_type":"variation","strand":1,"end":140536849,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs150490332","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140536851,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536851},{"id":"rs187795987","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536852,"source":"dbSNP","strand":1,"feature_type":"variation","end":140536852,"alleles":["G","A"]},{"end":140536855,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140536855,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1226405603"},{"alleles":["T","C"],"end":140536856,"feature_type":"variation","strand":1,"source":"dbSNP","start":140536856,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796473103"},{"seq_region_name":"7","id":"rs1350076531","clinical_significance":[],"strand":1,"feature_type":"variation","end":140536865,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536865,"source":"dbSNP"},{"end":140536868,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140536868,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1796473289","seq_region_name":"7"},{"source":"dbSNP","start":140536869,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140536869,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs975817134","seq_region_name":"7"},{"id":"rs970126438","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140536871,"strand":1,"feature_type":"variation","start":140536871,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1394528515","clinical_significance":[],"start":140536874,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140536874,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs921653382","clinical_significance":[],"alleles":["G","T"],"end":140536877,"strand":1,"feature_type":"variation","start":140536877,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536879,"feature_type":"variation","strand":1,"end":140536879,"alleles":["T","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585574383"},{"seq_region_name":"7","id":"rs1796473840","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536882,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140536882},{"source":"dbSNP","start":140536883,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140536883,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1401792737"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585574400","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140536886,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536886},{"seq_region_name":"7","id":"rs142328883","clinical_significance":[],"start":140536893,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["CC","C"],"end":140536894,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140536895,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536895,"source":"dbSNP","id":"rs1796474216","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536896,"feature_type":"variation","strand":1,"end":140536896,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs377243497"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796474398","end":140536897,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140536897,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140536899,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140536899,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs951736461","seq_region_name":"7","clinical_significance":[]},{"id":"rs931822444","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140536903,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536903,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140536907,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536907,"clinical_significance":[],"seq_region_name":"7","id":"rs983302113"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1014736407","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536910,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140536910},{"alleles":["C","T"],"end":140536912,"feature_type":"variation","strand":1,"source":"dbSNP","start":140536912,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796474891"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140536915,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536915,"clinical_significance":[],"id":"rs966015968","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130498279","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140536917,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536917},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536919,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140536919,"seq_region_name":"7","id":"rs1646301989","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796475085","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536923,"source":"dbSNP","strand":1,"feature_type":"variation","end":140536923,"alleles":["A","G"]},{"source":"dbSNP","start":140536924,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140536924,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796475185"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1489144610","source":"dbSNP","start":140536926,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140536926,"alleles":["G","T"],"feature_type":"variation","strand":1},{"id":"rs1796475360","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536928,"source":"dbSNP","strand":1,"feature_type":"variation","end":140536928,"alleles":["G","T"]},{"seq_region_name":"7","id":"rs1796475448","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536932,"source":"dbSNP","strand":1,"feature_type":"variation","end":140536932,"alleles":["G","A"]},{"alleles":["G","A"],"end":140536934,"strand":1,"feature_type":"variation","start":140536934,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1357959871","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","T"],"end":140536937,"strand":1,"feature_type":"variation","start":140536937,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1244475629","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796475758","clinical_significance":[],"end":140536941,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140536941,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536942,"source":"dbSNP","strand":1,"feature_type":"variation","end":140536942,"alleles":["C","T"],"id":"rs541122836","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140536943,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536943,"clinical_significance":[],"id":"rs192534312","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140536944,"alleles":["T","TT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536944,"clinical_significance":[],"id":"rs1796476042","seq_region_name":"7"},{"alleles":["G","A","C"],"end":140536945,"strand":1,"feature_type":"variation","start":140536945,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796476121","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536948,"source":"dbSNP","strand":1,"feature_type":"variation","end":140536948,"alleles":["C","T"],"id":"rs1269990410","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","A"],"end":140536949,"feature_type":"variation","strand":1,"source":"dbSNP","start":140536949,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1796476333","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796476405","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140536951,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536951},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796476498","source":"dbSNP","start":140536953,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140536953,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1796476575","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536962,"source":"dbSNP","strand":1,"feature_type":"variation","end":140536962,"alleles":["T","A"]},{"seq_region_name":"7","id":"rs1293123111","clinical_significance":[],"end":140536967,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140536967,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140536968,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140536972,"alleles":["TGTGT","TGT"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1226311526","seq_region_name":"7"},{"clinical_significance":[],"id":"rs914501174","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536973,"feature_type":"variation","strand":1,"end":140536973,"alleles":["T","C"]},{"alleles":["T","C"],"end":140536975,"strand":1,"feature_type":"variation","start":140536975,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs532943828","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1284105228","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536979,"feature_type":"variation","strand":1,"end":140536979,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs921993588","clinical_significance":[],"strand":1,"feature_type":"variation","end":140536980,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536980,"source":"dbSNP"},{"id":"rs1796477247","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140536982,"source":"dbSNP","strand":1,"feature_type":"variation","end":140536982,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1365840481","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140536987,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536987},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140536989,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140536989,"clinical_significance":[],"seq_region_name":"7","id":"rs2130498485"},{"strand":1,"feature_type":"variation","alleles":["TACTTA","TA"],"end":140537006,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537001,"source":"dbSNP","id":"rs1220777971","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140537002,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140537002,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1431640055"},{"seq_region_name":"7","id":"rs1391434119","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140537004,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537004,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs931965504","alleles":["T","C"],"end":140537005,"feature_type":"variation","strand":1,"source":"dbSNP","start":140537005,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140537007,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140537007,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1042428821"},{"id":"rs1796477962","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140537008,"strand":1,"feature_type":"variation","start":140537008,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140537010,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537010,"source":"dbSNP","seq_region_name":"7","id":"rs1200571238","clinical_significance":[]},{"start":140537012,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140537012,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796478166","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130498563","clinical_significance":[],"alleles":["A","C"],"end":140537013,"strand":1,"feature_type":"variation","start":140537013,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs902492315","feature_type":"variation","strand":1,"end":140537017,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537017},{"id":"rs1176243525","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140537018,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537018,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1796478697","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140537032,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537032},{"alleles":["CTAGACCT","CT"],"end":140537048,"strand":1,"feature_type":"variation","start":140537041,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796478797","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","-"],"end":140537045,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537045,"clinical_significance":[],"seq_region_name":"7","id":"rs1796478889"},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140537046,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537046,"clinical_significance":[],"id":"rs1434535504","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140537047,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537047,"clinical_significance":[],"seq_region_name":"7","id":"rs551417024"},{"strand":1,"feature_type":"variation","end":140537048,"alleles":["T","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537048,"source":"dbSNP","id":"rs1422688555","seq_region_name":"7","clinical_significance":[]},{"start":140537049,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140537049,"strand":1,"feature_type":"variation","id":"rs1796479256","seq_region_name":"7","clinical_significance":[]},{"start":140537053,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140537053,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796479341","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796479429","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537054,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140537054},{"alleles":["T","A"],"end":140537055,"strand":1,"feature_type":"variation","start":140537055,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796479528","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130498663","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140537059,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537059},{"clinical_significance":[],"seq_region_name":"7","id":"rs1484682351","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537062,"feature_type":"variation","strand":1,"end":140537062,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1796479720","clinical_significance":[],"start":140537066,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140537066,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1056486897","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537069,"feature_type":"variation","strand":1,"end":140537069,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1796479903","clinical_significance":[],"strand":1,"feature_type":"variation","end":140537076,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537076,"source":"dbSNP"},{"seq_region_name":"7","id":"rs376166976","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537077,"source":"dbSNP","strand":1,"feature_type":"variation","end":140537077,"alleles":["C","G"]},{"id":"rs1187127801","seq_region_name":"7","clinical_significance":[],"start":140537078,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140537078,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537080,"feature_type":"variation","strand":1,"end":140537080,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1249770086"},{"seq_region_name":"7","id":"rs1206766519","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537081,"source":"dbSNP","strand":1,"feature_type":"variation","end":140537081,"alleles":["G","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537082,"feature_type":"variation","strand":1,"end":140537082,"alleles":["T","G"],"clinical_significance":[],"id":"rs1585574802","seq_region_name":"7"},{"clinical_significance":[],"id":"rs895210164","seq_region_name":"7","source":"dbSNP","start":140537085,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140537085,"alleles":["C","T"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140537091,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537091,"source":"dbSNP","seq_region_name":"7","id":"rs6956815","clinical_significance":[]},{"start":140537093,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140537093,"alleles":["A","G"],"strand":1,"feature_type":"variation","id":"rs1796480755","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140537099,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537099,"source":"dbSNP","id":"rs1212045288","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537101,"source":"dbSNP","strand":1,"feature_type":"variation","end":140537101,"alleles":["C","T"],"id":"rs1796480921","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537102,"feature_type":"variation","strand":1,"end":140537102,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1028230979"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1278239305","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537103,"feature_type":"variation","strand":1,"end":140537103,"alleles":["G","T"]},{"seq_region_name":"7","id":"rs1796481214","clinical_significance":[],"end":140537108,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140537108,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1190697756","end":140537109,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140537109,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796481399","alleles":["C","G"],"end":140537116,"feature_type":"variation","strand":1,"source":"dbSNP","start":140537116,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140537123,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140537123,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1215201095"},{"seq_region_name":"7","id":"rs1796481576","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140537125,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537125,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1371588566","feature_type":"variation","strand":1,"end":140537127,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537127},{"seq_region_name":"7","id":"rs1295975837","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537129,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140537129},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537131,"source":"dbSNP","strand":1,"feature_type":"variation","end":140537131,"alleles":["A","G"],"seq_region_name":"7","id":"rs1796481862","clinical_significance":[]},{"end":140537134,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140537134,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1796481955","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140537136,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537136,"clinical_significance":[],"id":"rs115143435","seq_region_name":"7"},{"alleles":["G","T"],"end":140537142,"feature_type":"variation","strand":1,"source":"dbSNP","start":140537142,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs878903967","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1052581923","alleles":["G","A"],"end":140537144,"feature_type":"variation","strand":1,"source":"dbSNP","start":140537144,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1796482203","clinical_significance":[],"start":140537148,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140537148,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140537150,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537150,"clinical_significance":[],"seq_region_name":"7","id":"rs1304944388"},{"seq_region_name":"7","id":"rs1464898644","clinical_significance":[],"start":140537152,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140537152,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140537154,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537154,"clinical_significance":[],"seq_region_name":"7","id":"rs138519333"},{"feature_type":"variation","strand":1,"end":140537155,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537155,"clinical_significance":[],"seq_region_name":"7","id":"rs879306637"},{"clinical_significance":[],"id":"rs1796482649","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537155,"feature_type":"variation","strand":1,"end":140537156,"alleles":["CC","C"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537168,"source":"dbSNP","strand":1,"feature_type":"variation","end":140537168,"alleles":["C","A","T"],"seq_region_name":"7","id":"rs763590214","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796482739","source":"dbSNP","start":140537177,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140537177,"alleles":["C","G"],"feature_type":"variation","strand":1},{"start":140537181,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140537181,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796482822","clinical_significance":[]},{"source":"dbSNP","start":140537184,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140537184,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs966116152"},{"id":"rs1796483015","seq_region_name":"7","clinical_significance":[],"start":140537185,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140537185,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585574984","alleles":["A","G"],"end":140537190,"feature_type":"variation","strand":1,"source":"dbSNP","start":140537190,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1796483180","clinical_significance":[],"alleles":["C","T"],"end":140537193,"strand":1,"feature_type":"variation","start":140537193,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["A","G"],"end":140537199,"feature_type":"variation","strand":1,"source":"dbSNP","start":140537199,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796483280"},{"seq_region_name":"7","id":"rs1391496436","clinical_significance":[],"start":140537200,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140537200,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1186198060","clinical_significance":[],"start":140537203,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140537203,"alleles":["C","-"],"strand":1,"feature_type":"variation"},{"end":140537205,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","start":140537205,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796483569","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796483690","source":"dbSNP","start":140537206,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140537206,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140537212,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537212,"clinical_significance":[],"seq_region_name":"7","id":"rs975725498"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537213,"source":"dbSNP","strand":1,"feature_type":"variation","end":140537213,"alleles":["T","C"],"id":"rs1796483898","seq_region_name":"7","clinical_significance":[]},{"id":"rs1045717114","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140537217,"strand":1,"feature_type":"variation","start":140537217,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140537225,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140537225,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs921683969","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796484242","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537236,"source":"dbSNP","strand":1,"feature_type":"variation","end":140537236,"alleles":["T","A"]},{"strand":1,"feature_type":"variation","end":140537242,"alleles":["AAAAA","AAAA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537238,"source":"dbSNP","seq_region_name":"7","id":"rs1563124029","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1482169980","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140537240,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537240},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537244,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140537244,"clinical_significance":[],"seq_region_name":"7","id":"rs1312812246"},{"seq_region_name":"7","id":"rs567425191","clinical_significance":[],"strand":1,"feature_type":"variation","end":140537248,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537248,"source":"dbSNP"},{"start":140537253,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140537253,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs953075687","clinical_significance":[]},{"id":"rs534829145","seq_region_name":"7","clinical_significance":[],"start":140537254,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140537254,"strand":1,"feature_type":"variation"},{"end":140537257,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140537257,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796484931","clinical_significance":[]},{"end":140537263,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140537263,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1796485023","seq_region_name":"7","clinical_significance":[]},{"id":"rs1796485114","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537268,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140537268},{"seq_region_name":"7","id":"rs1272570836","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537274,"source":"dbSNP","strand":1,"feature_type":"variation","end":140537274,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1227844175","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537277,"feature_type":"variation","strand":1,"end":140537277,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796485394","end":140537281,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140537281,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1293839799","clinical_significance":[],"start":140537289,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140537289,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140537294,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140537299,"alleles":["TTATTT","TT"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs67106963"},{"end":140537298,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140537298,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796485718","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1233501027","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537302,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140537302},{"id":"rs1796485917","seq_region_name":"7","clinical_significance":[],"end":140537315,"alleles":["TATAT","TAT"],"strand":1,"feature_type":"variation","start":140537311,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1276173402","clinical_significance":[],"alleles":["A","G"],"end":140537312,"strand":1,"feature_type":"variation","start":140537312,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796486086","end":140537317,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140537317,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1345124610","seq_region_name":"7","alleles":["C","A"],"end":140537324,"feature_type":"variation","strand":1,"source":"dbSNP","start":140537324,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1796486280","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537327,"feature_type":"variation","strand":1,"end":140537327,"alleles":["G","A"]},{"source":"dbSNP","start":140537329,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140537329,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs2130499296","seq_region_name":"7"},{"seq_region_name":"7","id":"rs914385936","clinical_significance":[],"start":140537333,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140537333,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1796486493","seq_region_name":"7","source":"dbSNP","start":140537334,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140537334,"alleles":["A","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1796486581","seq_region_name":"7","source":"dbSNP","start":140537339,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140537345,"alleles":["TGTATGT","TGT"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs887538773","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537340,"source":"dbSNP","strand":1,"feature_type":"variation","end":140537340,"alleles":["G","A"]},{"id":"rs1796487093","seq_region_name":"7","clinical_significance":[],"start":140537343,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140537343,"strand":1,"feature_type":"variation"},{"start":140537346,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140537346,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs946006392","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585575181","feature_type":"variation","strand":1,"end":140537356,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537356},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537359,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140537359,"id":"rs1796487356","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140537360,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537360,"clinical_significance":[],"seq_region_name":"7","id":"rs1585575190"},{"seq_region_name":"7","id":"rs1042010331","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140537361,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537361,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537370,"feature_type":"variation","strand":1,"end":140537370,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1796487683"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537371,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140537371,"clinical_significance":[],"seq_region_name":"7","id":"rs1489207235"},{"source":"dbSNP","start":140537372,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140537372,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796487875"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537375,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140537375,"seq_region_name":"7","id":"rs1796487963","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537376,"feature_type":"variation","strand":1,"end":140537376,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1014782645"},{"seq_region_name":"7","id":"rs1796488128","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537382,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140537382},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537384,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140537384,"clinical_significance":[],"seq_region_name":"7","id":"rs1796488219"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537384,"feature_type":"variation","strand":1,"alleles":["AGTAGT","AGTAGTAGT"],"end":140537389,"clinical_significance":[],"seq_region_name":"7","id":"rs966268073"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537389,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140537389,"seq_region_name":"7","id":"rs976058370","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796488525","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537392,"source":"dbSNP","strand":1,"feature_type":"variation","end":140537392,"alleles":["A","G"]},{"feature_type":"variation","strand":1,"end":140537396,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537396,"clinical_significance":[],"seq_region_name":"7","id":"rs1796488617"},{"seq_region_name":"7","id":"rs1428586797","clinical_significance":[],"strand":1,"feature_type":"variation","end":140537401,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537401,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1796488786","clinical_significance":[],"end":140537405,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140537405,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1796488880","clinical_significance":[],"start":140537405,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140537408,"alleles":["TGGT","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1796488949","clinical_significance":[],"alleles":["TGGTTT","T"],"end":140537410,"strand":1,"feature_type":"variation","start":140537405,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537408,"feature_type":"variation","strand":1,"end":140537408,"alleles":["T","C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1796489037"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796489151","source":"dbSNP","start":140537409,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140537409,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796489247","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537410,"feature_type":"variation","strand":1,"alleles":["-","CA"],"end":140537409},{"source":"dbSNP","start":140537413,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140537413,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1029331865","seq_region_name":"7"},{"start":140537414,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140537414,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs953280023","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1199847942","end":140537415,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140537415,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1796489633","seq_region_name":"7","feature_type":"variation","strand":1,"end":140537417,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537417},{"strand":1,"feature_type":"variation","end":140537427,"alleles":["A","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537427,"source":"dbSNP","seq_region_name":"7","id":"rs979417621","clinical_significance":[]},{"start":140537428,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140537428,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1182713573","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537429,"feature_type":"variation","strand":1,"end":140537430,"alleles":["AA","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs925276259"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537430,"source":"dbSNP","strand":1,"feature_type":"variation","end":140537430,"alleles":["A","C","T"],"id":"rs1249955933","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs935443282","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537433,"source":"dbSNP","strand":1,"feature_type":"variation","end":140537433,"alleles":["C","T"]},{"end":140537443,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140537443,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1796490239","seq_region_name":"7"},{"end":140537450,"alleles":["TTTGTTTT","TTT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140537443,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs988184776"},{"seq_region_name":"7","id":"rs1173036885","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140537446,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537446,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1488867935","feature_type":"variation","strand":1,"alleles":["TTTTATTTTTTA","TTTTATTTTTTATTTTTTA"],"end":140537458,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537447},{"seq_region_name":"7","id":"rs1796490601","clinical_significance":[],"alleles":["T","C"],"end":140537450,"strand":1,"feature_type":"variation","start":140537450,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140537452,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140537452,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs542508620","clinical_significance":[]},{"seq_region_name":"7","id":"rs1267706345","clinical_significance":[],"alleles":["A","G"],"end":140537459,"strand":1,"feature_type":"variation","start":140537459,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140537460,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140537460,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs1796490864","seq_region_name":"7","clinical_significance":[]},{"end":140537463,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140537463,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs756918428","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140537464,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140537464,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585575350"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537465,"feature_type":"variation","strand":1,"alleles":["TTTTT","TTTT"],"end":140537469,"clinical_significance":[],"id":"rs949591946","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1289361477","seq_region_name":"7","alleles":["T","C"],"end":140537467,"feature_type":"variation","strand":1,"source":"dbSNP","start":140537467,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140537474,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140537474,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1796491258","seq_region_name":"7"},{"source":"dbSNP","start":140537478,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140537478,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs749930879","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140537483,"alleles":["A","C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537483,"source":"dbSNP","id":"rs1585575388","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs762170857","feature_type":"variation","strand":1,"alleles":["CCCCAGCTGGAGAGC","C"],"end":140537498,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537484},{"start":140537486,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140537486,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796491719","clinical_significance":[]},{"source":"dbSNP","start":140537487,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140537487,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1045196691"},{"id":"rs1796491948","seq_region_name":"7","clinical_significance":[],"start":140537488,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140537488,"strand":1,"feature_type":"variation"},{"end":140537489,"alleles":["G","GG"],"strand":1,"feature_type":"variation","start":140537489,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130499716","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140537491,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537491,"clinical_significance":[],"seq_region_name":"7","id":"rs1390839123"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130499733","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537496,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140537496},{"start":140537504,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140537504,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130499747","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796492132","clinical_significance":[],"start":140537504,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TGCA","TGCATGCA"],"end":140537507,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1295143782","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537506,"feature_type":"variation","strand":1,"end":140537506,"alleles":["C","T"]},{"alleles":["A","G"],"end":140537507,"strand":1,"feature_type":"variation","start":140537507,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796492319","clinical_significance":[]},{"end":140537514,"alleles":["AGTCATAG","AG"],"strand":1,"feature_type":"variation","start":140537507,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1456321458","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1367883348","source":"dbSNP","start":140537509,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140537509,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537509,"source":"dbSNP","strand":1,"feature_type":"variation","end":140537510,"alleles":["TC","-"],"seq_region_name":"7","id":"rs1796492610","clinical_significance":[]},{"start":140537510,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140537510,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796492694","clinical_significance":[]},{"end":140537511,"alleles":["A","G","T"],"strand":1,"feature_type":"variation","start":140537511,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1287541875","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537512,"feature_type":"variation","strand":1,"end":140537516,"alleles":["TAGCT","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1796492933"},{"seq_region_name":"7","id":"rs1056351562","clinical_significance":[],"end":140537514,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140537514,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1409983884","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537515,"source":"dbSNP","strand":1,"feature_type":"variation","end":140537515,"alleles":["C","A"]},{"source":"dbSNP","start":140537518,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140537518,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs895241062"},{"id":"rs1796493305","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537519,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140537519},{"clinical_significance":[],"seq_region_name":"7","id":"rs1433788662","source":"dbSNP","start":140537525,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140537525,"alleles":["T","C"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537528,"source":"dbSNP","strand":1,"feature_type":"variation","end":140537528,"alleles":["A","C"],"seq_region_name":"7","id":"rs1796493490","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796493591","source":"dbSNP","start":140537530,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140537530,"alleles":["C","G"],"feature_type":"variation","strand":1},{"start":140537531,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140537531,"alleles":["T","G"],"strand":1,"feature_type":"variation","id":"rs1796493678","seq_region_name":"7","clinical_significance":[]},{"id":"rs1736006012","seq_region_name":"7","clinical_significance":[],"end":140537534,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140537534,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537535,"source":"dbSNP","strand":1,"feature_type":"variation","end":140537535,"alleles":["G","A"],"id":"rs1269566906","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140537540,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140537540,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1048787282"},{"feature_type":"variation","strand":1,"end":140537541,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537541,"clinical_significance":[],"seq_region_name":"7","id":"rs1796493934"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537542,"source":"dbSNP","strand":1,"feature_type":"variation","end":140537542,"alleles":["C","A","T"],"id":"rs948137049","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130499912","end":140537543,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140537543,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs781181206","clinical_significance":[],"alleles":["G","A"],"end":140537545,"strand":1,"feature_type":"variation","start":140537545,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537546,"feature_type":"variation","strand":1,"end":140537546,"alleles":["A","T"],"clinical_significance":[],"id":"rs1585575584","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537552,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140537552,"seq_region_name":"7","id":"rs184507109","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140537558,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537558,"clinical_significance":[],"seq_region_name":"7","id":"rs571335135"},{"seq_region_name":"7","id":"rs1796494497","clinical_significance":[],"start":140537559,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140537559,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"alleles":["G","C"],"end":140537560,"feature_type":"variation","strand":1,"source":"dbSNP","start":140537560,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1015078660"},{"seq_region_name":"7","id":"rs1585575638","clinical_significance":[],"start":140537565,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140537565,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140537566,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537566,"clinical_significance":[],"seq_region_name":"7","id":"rs188198341"},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140537568,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537568,"clinical_significance":[],"seq_region_name":"7","id":"rs192759863"},{"seq_region_name":"7","id":"rs1237878237","clinical_significance":[],"alleles":["G","A"],"end":140537572,"strand":1,"feature_type":"variation","start":140537572,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140537572,"alleles":["G","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140537572,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796495037"},{"source":"dbSNP","start":140537574,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140537574,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1309315998","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796495235","end":140537578,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140537578,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140537581,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537581,"source":"dbSNP","seq_region_name":"7","id":"rs1318710660","clinical_significance":[]},{"seq_region_name":"7","id":"rs901556436","clinical_significance":[],"strand":1,"feature_type":"variation","end":140537593,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537593,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1302744221","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140537594,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537594,"source":"dbSNP"},{"seq_region_name":"7","id":"rs557382890","clinical_significance":[],"strand":1,"feature_type":"variation","end":140537596,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537596,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537598,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140537598,"clinical_significance":[],"seq_region_name":"7","id":"rs1796495706"},{"end":140537603,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140537603,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1389892689","clinical_significance":[]},{"source":"dbSNP","start":140537604,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140537604,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796495896"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537605,"feature_type":"variation","strand":1,"end":140537605,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1796495980"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140537611,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537611,"source":"dbSNP","seq_region_name":"7","id":"rs1028799879","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537613,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140537613,"seq_region_name":"7","id":"rs2130500085","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130500091","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140537615,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537615},{"id":"rs575851473","seq_region_name":"7","clinical_significance":[],"end":140537622,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140537622,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796496252","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537627,"feature_type":"variation","strand":1,"end":140537627,"alleles":["A","G"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537630,"source":"dbSNP","strand":1,"feature_type":"variation","end":140537630,"alleles":["A","T"],"seq_region_name":"7","id":"rs1458575613","clinical_significance":[]},{"seq_region_name":"7","id":"rs953326404","clinical_significance":[],"start":140537631,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140537631,"alleles":["C","G","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796496413","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537636,"feature_type":"variation","strand":1,"end":140537637,"alleles":["TC","-"]},{"feature_type":"variation","strand":1,"end":140537640,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537640,"clinical_significance":[],"seq_region_name":"7","id":"rs2130500145"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585575786","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537642,"feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140537642},{"seq_region_name":"7","id":"rs2130500166","clinical_significance":[],"start":140537644,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140537644,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1005023484","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140537650,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537650,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140537655,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537655,"clinical_significance":[],"seq_region_name":"7","id":"rs1796496703"},{"seq_region_name":"7","id":"rs1000721818","clinical_significance":[],"start":140537657,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140537657,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796496870","feature_type":"variation","strand":1,"end":140537659,"alleles":["TT","TTCGTT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537658},{"clinical_significance":[],"seq_region_name":"7","id":"rs10653353","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537658,"feature_type":"variation","strand":1,"end":140537684,"alleles":["TTTGTTTGTTTGTTTGTTTGTTTGTTT","TTTGTTTGTTTGTTTGTTT","TTTGTTTGTTTGTTTGTTTGTTT","TTTGTTTGTTTGTTTGTTTGTTTGTTTGTTT","TTTGTTTGTTTGTTTGTTTGTTTGTTTGTTTGTTT","TTTGTTTGTTTGTTTGTTTGTTTGTTTGTTTGTTTGTTT","TTTGTTTGTTTGTTTGTTTGTTTGTTTGTTTGTTTGTTTGTTT","TTTGTTTGTTTGTTTGTTTGTTTGTTTGTTTGTTTGTTTGTTTGTTTGTTT"]},{"alleles":["T","G"],"end":140537660,"strand":1,"feature_type":"variation","start":140537660,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796497341","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796497427","clinical_significance":[],"alleles":["G","A"],"end":140537661,"strand":1,"feature_type":"variation","start":140537661,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs762369107","clinical_significance":[],"start":140537662,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140537664,"alleles":["TTT","TT"],"strand":1,"feature_type":"variation"},{"alleles":["T","C"],"end":140537663,"feature_type":"variation","strand":1,"source":"dbSNP","start":140537663,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796497602"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537666,"source":"dbSNP","strand":1,"feature_type":"variation","end":140537666,"alleles":["T","A","C"],"seq_region_name":"7","id":"rs956699205","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796497784","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537667,"feature_type":"variation","strand":1,"end":140537667,"alleles":["T","C"]},{"clinical_significance":[],"id":"rs1796497894","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537673,"feature_type":"variation","strand":1,"end":140537673,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs11772120","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537674,"source":"dbSNP","strand":1,"feature_type":"variation","end":140537674,"alleles":["T","A"]},{"alleles":["T","C"],"end":140537676,"strand":1,"feature_type":"variation","start":140537676,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796498060","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1201441283","feature_type":"variation","strand":1,"alleles":["TTTT","-"],"end":140537685,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537682},{"clinical_significance":[],"seq_region_name":"7","id":"rs1345260362","feature_type":"variation","strand":1,"end":140537685,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537685},{"end":140537692,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140537692,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796498330"},{"end":140537694,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140537694,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1257438225"},{"clinical_significance":[],"id":"rs988068872","seq_region_name":"7","source":"dbSNP","start":140537696,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140537696,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537699,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140537699,"clinical_significance":[],"id":"rs1796498594","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs542853320","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537706,"feature_type":"variation","strand":1,"end":140537706,"alleles":["G","A","T"]},{"source":"dbSNP","start":140537710,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140537710,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1298175064"},{"seq_region_name":"7","id":"rs1796498799","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140537714,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537714,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796498886","feature_type":"variation","strand":1,"end":140537721,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537721},{"source":"dbSNP","start":140537723,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140537723,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs970813905","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1015612175","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537726,"feature_type":"variation","strand":1,"end":140537726,"alleles":["A","C"]},{"seq_region_name":"7","id":"rs1467281755","clinical_significance":[],"start":140537727,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140537727,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140537731,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537731,"clinical_significance":[],"seq_region_name":"7","id":"rs1796499251"},{"seq_region_name":"7","id":"rs564114213","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537734,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140537734},{"alleles":["A","G"],"end":140537739,"feature_type":"variation","strand":1,"source":"dbSNP","start":140537739,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs997194373"},{"alleles":["A","G","T"],"end":140537743,"feature_type":"variation","strand":1,"source":"dbSNP","start":140537743,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1028653562","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537747,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140537747,"clinical_significance":[],"seq_region_name":"7","id":"rs1796499631"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796499782","source":"dbSNP","start":140537748,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140537748,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140537750,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537750,"clinical_significance":[],"seq_region_name":"7","id":"rs1390867118"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537750,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","-"],"end":140537750,"seq_region_name":"7","id":"rs1465557014","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537754,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140537754,"seq_region_name":"7","id":"rs780431121","clinical_significance":[]},{"end":140537756,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140537756,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130500428","clinical_significance":[]},{"start":140537758,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140537758,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1170633622","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796500406","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537759,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140537759},{"seq_region_name":"7","id":"rs184257096","clinical_significance":[],"start":140537764,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140537764,"strand":1,"feature_type":"variation"},{"end":140537767,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140537767,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs990285256","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796500659","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537776,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140537776},{"id":"rs541163805","seq_region_name":"7","clinical_significance":[],"start":140537778,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140537778,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537782,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140537782,"seq_region_name":"7","id":"rs1188647105","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs367719427","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537783,"feature_type":"variation","strand":1,"end":140537783,"alleles":["C","A","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537784,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140537784,"id":"rs747372578","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs908910106","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140537787,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537787},{"seq_region_name":"7","id":"rs1346436560","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537788,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140537788},{"start":140537789,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140537789,"alleles":["C","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs188924639","clinical_significance":[]},{"id":"rs1796501438","seq_region_name":"7","clinical_significance":[],"start":140537790,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140537790,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1230050419","seq_region_name":"7","feature_type":"variation","strand":1,"end":140537803,"alleles":["ACCATGCCCGACC","ACC"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537791},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537795,"source":"dbSNP","strand":1,"feature_type":"variation","end":140537795,"alleles":["T","C"],"id":"rs1796501527","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1339936800","clinical_significance":[],"start":140537798,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140537798,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537799,"source":"dbSNP","strand":1,"feature_type":"variation","end":140537799,"alleles":["C","T"],"seq_region_name":"7","id":"rs141492996","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140537800,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537800,"source":"dbSNP","seq_region_name":"7","id":"rs2130500610","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140537802,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537802,"clinical_significance":[],"id":"rs1796501797","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537804,"feature_type":"variation","strand":1,"end":140537804,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1439679731"},{"feature_type":"variation","strand":1,"end":140537815,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537815,"clinical_significance":[],"seq_region_name":"7","id":"rs1796501942"},{"seq_region_name":"7","id":"rs1342055885","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C","G","T"],"end":140537825,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537825,"source":"dbSNP"},{"id":"rs1796502444","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537826,"source":"dbSNP","strand":1,"feature_type":"variation","end":140537826,"alleles":["T","C"]},{"feature_type":"variation","strand":1,"end":140537828,"alleles":["T","C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537828,"clinical_significance":[],"seq_region_name":"7","id":"rs901605733"},{"alleles":["T","C"],"end":140537830,"feature_type":"variation","strand":1,"source":"dbSNP","start":140537830,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs544954965"},{"clinical_significance":[],"seq_region_name":"7","id":"rs563445809","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537836,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140537836},{"end":140537837,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140537837,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs551500633"},{"clinical_significance":[],"seq_region_name":"7","id":"rs78619203","end":140537842,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140537842,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1427955473","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140537843,"strand":1,"feature_type":"variation","start":140537843,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537849,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140537849,"clinical_significance":[],"seq_region_name":"7","id":"rs1585576265"},{"end":140537852,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140537852,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1049626122","seq_region_name":"7"},{"start":140537853,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140537853,"strand":1,"feature_type":"variation","id":"rs887847660","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","A"],"end":140537854,"feature_type":"variation","strand":1,"source":"dbSNP","start":140537854,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs549004733"},{"source":"dbSNP","start":140537859,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140537859,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1796503678","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140537862,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537862,"clinical_significance":[],"seq_region_name":"7","id":"rs1796503771"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140537863,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537863,"source":"dbSNP","id":"rs2130500734","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537866,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140537866,"seq_region_name":"7","id":"rs1367093299","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs755393615","alleles":["T","C"],"end":140537875,"feature_type":"variation","strand":1,"source":"dbSNP","start":140537875,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140537886,"alleles":["AC","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140537885,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1187367520"},{"seq_region_name":"7","id":"rs145264758","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537888,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140537888},{"clinical_significance":[],"seq_region_name":"7","id":"rs1252153518","source":"dbSNP","start":140537890,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140537890,"alleles":["G","C"],"feature_type":"variation","strand":1},{"end":140537896,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140537896,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs112404859"},{"seq_region_name":"7","id":"rs956584240","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537900,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140537900},{"seq_region_name":"7","id":"rs1796504540","clinical_significance":[],"alleles":["A","G"],"end":140537909,"strand":1,"feature_type":"variation","start":140537909,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140537912,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140537912,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1481799680","clinical_significance":[]},{"seq_region_name":"7","id":"rs997763601","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537922,"source":"dbSNP","strand":1,"feature_type":"variation","end":140537922,"alleles":["A","G"]},{"alleles":["G","A"],"end":140537924,"strand":1,"feature_type":"variation","start":140537924,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1796504822","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["TT","TTT"],"end":140537926,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537925,"clinical_significance":[],"id":"rs1796504902","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537926,"source":"dbSNP","strand":1,"feature_type":"variation","end":140537926,"alleles":["T","C"],"id":"rs1796504994","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1024946956","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537927,"source":"dbSNP","strand":1,"feature_type":"variation","end":140537927,"alleles":["C","T"]},{"feature_type":"variation","strand":1,"end":140537937,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537937,"clinical_significance":[],"seq_region_name":"7","id":"rs2130500830"},{"source":"dbSNP","start":140537939,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140537939,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1796505205","seq_region_name":"7"},{"end":140537940,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","start":140537940,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1358463276","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1796505437","seq_region_name":"7","source":"dbSNP","start":140537941,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140537941,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140537943,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537943,"clinical_significance":[],"id":"rs546711114","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs181620224","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537946,"feature_type":"variation","strand":1,"end":140537946,"alleles":["G","C"]},{"seq_region_name":"7","id":"rs1232501464","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140537947,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537947,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537948,"source":"dbSNP","strand":1,"feature_type":"variation","end":140537948,"alleles":["G","A","C"],"seq_region_name":"7","id":"rs538662330","clinical_significance":[]},{"clinical_significance":[],"id":"rs1796505978","seq_region_name":"7","source":"dbSNP","start":140537950,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140537950,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537950,"feature_type":"variation","strand":1,"alleles":["GGG","GG"],"end":140537952,"clinical_significance":[],"seq_region_name":"7","id":"rs1408028021"},{"strand":1,"feature_type":"variation","end":140537951,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537951,"source":"dbSNP","seq_region_name":"7","id":"rs1796506183","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796506261","clinical_significance":[],"strand":1,"feature_type":"variation","end":140537952,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140537952,"source":"dbSNP"},{"alleles":["G","A"],"end":140537954,"strand":1,"feature_type":"variation","start":140537954,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs971248608","clinical_significance":[]},{"start":140537956,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140537956,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130500934","clinical_significance":[]},{"alleles":["G","C"],"end":140537957,"feature_type":"variation","strand":1,"source":"dbSNP","start":140537957,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs980860513"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1407572756","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140537968,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537968},{"seq_region_name":"7","id":"rs1389282991","clinical_significance":[],"end":140537973,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140537973,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1481664783","end":140537975,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140537975,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140537978,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140537978,"clinical_significance":[],"seq_region_name":"7","id":"rs781371567"},{"source":"dbSNP","start":140537990,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140537990,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1164632021"},{"source":"dbSNP","start":140537993,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140537993,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs184725579"},{"id":"rs1796507169","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140538004,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538004,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1796507270","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140538005,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538005,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1412186900","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538007,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140538007},{"seq_region_name":"7","id":"rs1183912888","clinical_significance":[],"alleles":["T","C"],"end":140538013,"strand":1,"feature_type":"variation","start":140538013,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1471285317","end":140538016,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140538016,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538019,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140538019,"seq_region_name":"7","id":"rs555598353","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538022,"feature_type":"variation","strand":1,"end":140538022,"alleles":["T","A"],"clinical_significance":[],"id":"rs984253631","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs115022100","source":"dbSNP","start":140538023,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140538023,"feature_type":"variation","strand":1},{"end":140538027,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140538027,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130501058"},{"feature_type":"variation","strand":1,"end":140538033,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538033,"clinical_significance":[],"seq_region_name":"7","id":"rs1190576216"},{"strand":1,"feature_type":"variation","end":140538034,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538034,"source":"dbSNP","seq_region_name":"7","id":"rs1287688144","clinical_significance":[]},{"id":"rs1416128721","seq_region_name":"7","clinical_significance":[],"start":140538037,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","G","T"],"end":140538037,"strand":1,"feature_type":"variation"},{"end":140538040,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140538040,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796508354"},{"alleles":["G","A"],"end":140538046,"strand":1,"feature_type":"variation","start":140538046,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs940230341","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796508565","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538050,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140538050},{"source":"dbSNP","start":140538056,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140538056,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796508666"},{"id":"rs1796508743","seq_region_name":"7","clinical_significance":[],"start":140538058,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140538058,"strand":1,"feature_type":"variation"},{"start":140538060,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140538060,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1563124494","clinical_significance":[]},{"start":140538062,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140538062,"strand":1,"feature_type":"variation","id":"rs1021810250","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140538069,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140538069,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796509032"},{"seq_region_name":"7","id":"rs1796509134","clinical_significance":[],"end":140538070,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140538070,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140538076,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538076,"source":"dbSNP","id":"rs1796509227","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","G"],"end":140538083,"feature_type":"variation","strand":1,"source":"dbSNP","start":140538083,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796509332"},{"seq_region_name":"7","id":"rs1226803426","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538085,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140538085},{"source":"dbSNP","start":140538089,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140538093,"alleles":["AAAAA","AAAA"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1372959683"},{"seq_region_name":"7","id":"rs1460659873","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538090,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140538090},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796509693","feature_type":"variation","strand":1,"end":140538093,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538093},{"feature_type":"variation","strand":1,"end":140538095,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538095,"clinical_significance":[],"seq_region_name":"7","id":"rs1796509777"},{"clinical_significance":[],"id":"rs1036468726","seq_region_name":"7","end":140538105,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140538105,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140538111,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538111,"clinical_significance":[],"seq_region_name":"7","id":"rs967115568"},{"seq_region_name":"7","id":"rs1438762644","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538112,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140538112},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140538113,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538113,"source":"dbSNP","seq_region_name":"7","id":"rs922946884","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538115,"feature_type":"variation","strand":1,"end":140538119,"alleles":["TTTTT","TTTT"],"clinical_significance":[],"seq_region_name":"7","id":"rs1355865369"},{"end":140538120,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140538120,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs977665445","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538121,"source":"dbSNP","strand":1,"feature_type":"variation","end":140538121,"alleles":["G","C"],"seq_region_name":"7","id":"rs1796510441","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140538124,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538124,"source":"dbSNP","seq_region_name":"7","id":"rs538078562","clinical_significance":[]},{"seq_region_name":"7","id":"rs1458041889","clinical_significance":[],"alleles":["T","G"],"end":140538128,"strand":1,"feature_type":"variation","start":140538128,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140538129,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538129,"source":"dbSNP","seq_region_name":"7","id":"rs1297071206","clinical_significance":[]},{"id":"rs1050176957","seq_region_name":"7","clinical_significance":[],"start":140538134,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140538134,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538135,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140538135,"seq_region_name":"7","id":"rs2130501308","clinical_significance":[]},{"clinical_significance":[],"id":"rs959972428","seq_region_name":"7","alleles":["C","G","T"],"end":140538136,"feature_type":"variation","strand":1,"source":"dbSNP","start":140538136,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["TTTT","TTT"],"end":140538140,"feature_type":"variation","strand":1,"source":"dbSNP","start":140538137,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796511078"},{"clinical_significance":[],"seq_region_name":"7","id":"rs888831962","source":"dbSNP","start":140538138,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140538138,"alleles":["T","C"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140538141,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538141,"source":"dbSNP","seq_region_name":"7","id":"rs750211385","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140538145,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538145,"source":"dbSNP","seq_region_name":"7","id":"rs2130501350","clinical_significance":[]},{"source":"dbSNP","start":140538148,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140538148,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1379863269"},{"seq_region_name":"7","id":"rs748413645","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538149,"source":"dbSNP","strand":1,"feature_type":"variation","end":140538149,"alleles":["T","C"]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140538150,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538150,"clinical_significance":[],"seq_region_name":"7","id":"rs1478741088"},{"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140538153,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538153,"clinical_significance":[],"id":"rs1796511745","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1251013138","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140538158,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538158},{"alleles":["G","C"],"end":140538159,"feature_type":"variation","strand":1,"source":"dbSNP","start":140538159,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796511930"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538160,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140538160,"seq_region_name":"7","id":"rs1796512017","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796512110","source":"dbSNP","start":140538163,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140538163,"alleles":["T","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1192952185","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538172,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140538172},{"source":"dbSNP","start":140538175,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140538175,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1796512289","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs915799877","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538176,"feature_type":"variation","strand":1,"end":140538176,"alleles":["C","T"]},{"start":140538177,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140538177,"strand":1,"feature_type":"variation","id":"rs948075496","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1269783941","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538178,"source":"dbSNP","strand":1,"feature_type":"variation","end":140538177,"alleles":["-","ATGGCAC"]},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140538186,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538186,"source":"dbSNP","seq_region_name":"7","id":"rs1291275864","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538187,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140538187,"seq_region_name":"7","id":"rs1796512758","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140538192,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538192,"source":"dbSNP","id":"rs1354583592","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796512950","end":140538196,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140538196,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1279654788","feature_type":"variation","strand":1,"end":140538201,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538201},{"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140538203,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538203,"clinical_significance":[],"seq_region_name":"7","id":"rs1000658650"},{"seq_region_name":"7","id":"rs1796513251","clinical_significance":[],"start":140538204,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140538204,"strand":1,"feature_type":"variation"},{"id":"rs16882335","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140538206,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538206,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1436458126","clinical_significance":[],"start":140538207,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140538207,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs540531917","seq_region_name":"7","source":"dbSNP","start":140538208,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140538208,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140538212,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538212,"source":"dbSNP","id":"rs375317533","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140538217,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140538217,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1025419766"},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140538219,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538219,"source":"dbSNP","seq_region_name":"7","id":"rs1796513927","clinical_significance":[]},{"id":"rs906530514","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140538221,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538221,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538223,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140538223,"clinical_significance":[],"id":"rs749343344","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1176365413","alleles":["G","T"],"end":140538225,"feature_type":"variation","strand":1,"source":"dbSNP","start":140538225,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1036975114","feature_type":"variation","strand":1,"end":140538231,"alleles":["G","A","C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538231},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796514309","alleles":["G","A"],"end":140538233,"feature_type":"variation","strand":1,"source":"dbSNP","start":140538233,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796514407","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538235,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140538235},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796514487","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140538242,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538242},{"start":140538244,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140538244,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs780162762","clinical_significance":[]},{"clinical_significance":[],"id":"rs1392733140","seq_region_name":"7","end":140538245,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140538245,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs368109082","clinical_significance":[],"start":140538246,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140538246,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["GGGGG","GGGG"],"end":140538250,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538246,"clinical_significance":[],"seq_region_name":"7","id":"rs1796514884"},{"strand":1,"feature_type":"variation","end":140538248,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538248,"source":"dbSNP","id":"rs12703989","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140538249,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538249,"source":"dbSNP","id":"rs1796515168","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","T"],"end":140538250,"feature_type":"variation","strand":1,"source":"dbSNP","start":140538250,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs952732064"},{"clinical_significance":[],"id":"rs1249876718","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140538253,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538253},{"strand":1,"feature_type":"variation","alleles":["C","CTTAGC"],"end":140538257,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538257,"source":"dbSNP","seq_region_name":"7","id":"rs1184528605","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs563869165","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140538259,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538259},{"start":140538264,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140538264,"strand":1,"feature_type":"variation","id":"rs1796515636","seq_region_name":"7","clinical_significance":[]},{"id":"rs1796515717","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538270,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140538270},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796515804","feature_type":"variation","strand":1,"end":140538272,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538272},{"alleles":["G","A"],"end":140538273,"strand":1,"feature_type":"variation","start":140538273,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585577066","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538274,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140538274,"clinical_significance":[],"seq_region_name":"7","id":"rs1250809391"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1050676593","source":"dbSNP","start":140538275,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140538275,"alleles":["A","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1796516192","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538276,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140538276},{"end":140538277,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140538277,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs889347340","seq_region_name":"7"},{"seq_region_name":"7","id":"rs961956087","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140538278,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538278,"source":"dbSNP"},{"clinical_significance":[],"id":"rs10275801","seq_region_name":"7","source":"dbSNP","start":140538281,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140538281,"alleles":["T","C"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538282,"feature_type":"variation","strand":1,"end":140538282,"alleles":["C","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1279683347"},{"seq_region_name":"7","id":"rs1229289058","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140538286,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538286,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1344895404","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538287,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140538287},{"strand":1,"feature_type":"variation","end":140538288,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538288,"source":"dbSNP","id":"rs1796516960","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","G","T"],"end":140538296,"feature_type":"variation","strand":1,"source":"dbSNP","start":140538296,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs922965367"},{"source":"dbSNP","start":140538297,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140538297,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs114836092"},{"seq_region_name":"7","id":"rs1303001447","clinical_significance":[],"start":140538298,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140538298,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140538303,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538303,"clinical_significance":[],"seq_region_name":"7","id":"rs768617243"},{"seq_region_name":"7","id":"rs1475094131","clinical_significance":[],"strand":1,"feature_type":"variation","end":140538304,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538304,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1194782320","clinical_significance":[],"start":140538305,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140538305,"strand":1,"feature_type":"variation"},{"alleles":["A","T"],"end":140538306,"feature_type":"variation","strand":1,"source":"dbSNP","start":140538306,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130501913"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538307,"feature_type":"variation","strand":1,"end":140538307,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130501927"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796518791","source":"dbSNP","start":140538308,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","-"],"end":140538308,"feature_type":"variation","strand":1},{"end":140538310,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140538310,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796518920","clinical_significance":[]},{"seq_region_name":"7","id":"rs1421249706","clinical_significance":[],"start":140538312,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140538312,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs986162324","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140538313,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538313,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538315,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140538315,"seq_region_name":"7","id":"rs1796519372","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140538316,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538316,"source":"dbSNP","seq_region_name":"7","id":"rs1796519508","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs998598373","feature_type":"variation","strand":1,"end":140538318,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538318},{"feature_type":"variation","strand":1,"end":140538320,"alleles":["A","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538320,"clinical_significance":[],"seq_region_name":"7","id":"rs1585577299"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1035517307","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538322,"feature_type":"variation","strand":1,"end":140538322,"alleles":["G","A"]},{"source":"dbSNP","start":140538327,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140538327,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796520068"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140538328,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538328,"clinical_significance":[],"seq_region_name":"7","id":"rs1796520205"},{"clinical_significance":[],"seq_region_name":"7","id":"rs777907581","source":"dbSNP","start":140538332,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140538332,"alleles":["C","G","T"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538332,"source":"dbSNP","strand":1,"feature_type":"variation","end":140538351,"alleles":["CATGCCCTGTTCCATGCCCT","CATGCCCT"],"seq_region_name":"7","id":"rs1429879116","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140538335,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538335,"clinical_significance":[],"seq_region_name":"7","id":"rs115821570"},{"strand":1,"feature_type":"variation","end":140538336,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538336,"source":"dbSNP","seq_region_name":"7","id":"rs1796521276","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1414246547","feature_type":"variation","strand":1,"end":140538340,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538340},{"clinical_significance":[],"seq_region_name":"7","id":"rs1183439396","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140538349,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538349},{"clinical_significance":[],"seq_region_name":"7","id":"rs1484799247","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140538350,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538350},{"alleles":["A","C"],"end":140538353,"strand":1,"feature_type":"variation","start":140538353,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796521885","clinical_significance":[]},{"source":"dbSNP","start":140538359,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140538359,"alleles":["T","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1257123607","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1205907998","feature_type":"variation","strand":1,"end":140538364,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538364},{"seq_region_name":"7","id":"rs1169198569","clinical_significance":[],"end":140538369,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140538369,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1796522512","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538374,"source":"dbSNP","strand":1,"feature_type":"variation","end":140538374,"alleles":["G","T"]},{"clinical_significance":[],"id":"rs1796522657","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538374,"feature_type":"variation","strand":1,"alleles":["GG","G"],"end":140538375},{"seq_region_name":"7","id":"rs1250069073","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538375,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140538375},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130502131","source":"dbSNP","start":140538377,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140538377,"feature_type":"variation","strand":1},{"start":140538380,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G","T"],"end":140538380,"strand":1,"feature_type":"variation","id":"rs761486200","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538385,"feature_type":"variation","strand":1,"end":140538385,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs55769135"},{"seq_region_name":"7","id":"rs1796523372","clinical_significance":[],"strand":1,"feature_type":"variation","end":140538388,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538388,"source":"dbSNP"},{"seq_region_name":"7","id":"rs945324530","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140538395,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538395,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1227014054","clinical_significance":[],"start":140538400,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140538400,"alleles":["C","A","T"],"strand":1,"feature_type":"variation"},{"start":140538402,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140538402,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796523872","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538406,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140538406,"clinical_significance":[],"seq_region_name":"7","id":"rs749889091"},{"clinical_significance":[],"id":"rs10254745","seq_region_name":"7","source":"dbSNP","start":140538407,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140538407,"alleles":["G","A"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538408,"source":"dbSNP","strand":1,"feature_type":"variation","end":140538408,"alleles":["T","A","C"],"seq_region_name":"7","id":"rs1796524478","clinical_significance":[]},{"start":140538411,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140538411,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796524661","clinical_significance":[]},{"alleles":["C","A","T"],"end":140538412,"feature_type":"variation","strand":1,"source":"dbSNP","start":140538412,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796524807"},{"seq_region_name":"7","id":"rs190566917","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538413,"source":"dbSNP","strand":1,"feature_type":"variation","end":140538413,"alleles":["G","A","C"]},{"id":"rs1796525259","seq_region_name":"7","clinical_significance":[],"start":140538417,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140538417,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796525362","end":140538420,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140538420,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1271680049","clinical_significance":[],"strand":1,"feature_type":"variation","end":140538425,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538425,"source":"dbSNP"},{"seq_region_name":"7","id":"rs752110199","clinical_significance":[],"strand":1,"feature_type":"variation","end":140538426,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538426,"source":"dbSNP"},{"source":"dbSNP","start":140538430,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140538430,"alleles":["G","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs750795672"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538430,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140538430,"clinical_significance":[],"seq_region_name":"7","id":"rs1033653901"},{"id":"rs1461408666","seq_region_name":"7","clinical_significance":[],"start":140538432,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140538432,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140538433,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140538433,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1213012960","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140538441,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538441,"clinical_significance":[],"seq_region_name":"7","id":"rs1295030694"},{"alleles":["C","A"],"end":140538444,"feature_type":"variation","strand":1,"source":"dbSNP","start":140538444,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs368107523"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538444,"source":"dbSNP","strand":1,"feature_type":"variation","end":140538447,"alleles":["CCCC","CCC"],"id":"rs1796526210","seq_region_name":"7","clinical_significance":[]},{"id":"rs1005623693","seq_region_name":"7","clinical_significance":[],"alleles":["C","G"],"end":140538446,"strand":1,"feature_type":"variation","start":140538446,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140538456,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140538456,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs7795622","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796526555","alleles":["G","A"],"end":140538457,"feature_type":"variation","strand":1,"source":"dbSNP","start":140538457,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1796526651","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["GGGG","GGGGG"],"end":140538460,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538457,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538458,"source":"dbSNP","strand":1,"feature_type":"variation","end":140538458,"alleles":["G","A"],"seq_region_name":"7","id":"rs1183175940","clinical_significance":[]},{"start":140538460,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140538460,"alleles":["G","C"],"strand":1,"feature_type":"variation","id":"rs1796526740","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs961561117","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538461,"feature_type":"variation","strand":1,"end":140538461,"alleles":["A","T"]},{"seq_region_name":"7","id":"rs1248506746","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538465,"source":"dbSNP","strand":1,"feature_type":"variation","end":140538465,"alleles":["G","A"]},{"alleles":["G","T"],"end":140538466,"feature_type":"variation","strand":1,"source":"dbSNP","start":140538466,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796527024"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538467,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140538467,"id":"rs1796527121","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140538469,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538469,"source":"dbSNP","seq_region_name":"7","id":"rs781500375","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1195363354","feature_type":"variation","strand":1,"end":140538470,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538470},{"alleles":["C","T"],"end":140538474,"strand":1,"feature_type":"variation","start":140538474,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1489082503","seq_region_name":"7","clinical_significance":[]},{"start":140538479,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C","T"],"end":140538479,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796527488","clinical_significance":[]},{"source":"dbSNP","start":140538491,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140538491,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796527622"},{"start":140538492,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140538492,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585577607","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140538498,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538498,"source":"dbSNP","seq_region_name":"7","id":"rs1796527791","clinical_significance":[]},{"clinical_significance":[],"id":"rs1278843645","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["TTTTTT","TTTTTTT"],"end":140538503,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538498},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538502,"feature_type":"variation","strand":1,"end":140538502,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1485610267"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796528106","source":"dbSNP","start":140538506,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140538506,"alleles":["T","C"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140538508,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140538508,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796528184"},{"clinical_significance":[],"seq_region_name":"7","id":"rs972129093","feature_type":"variation","strand":1,"alleles":["T","A"],"end":140538511,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538511},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538512,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140538512,"seq_region_name":"7","id":"rs1796528380","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796528481","clinical_significance":[],"start":140538513,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140538513,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1796528573","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140538514,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538514},{"clinical_significance":[],"seq_region_name":"7","id":"rs1244176297","feature_type":"variation","strand":1,"alleles":["TTTTTTT","TTTTTT","TTTTTTTT"],"end":140538520,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538514},{"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140538516,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538516,"source":"dbSNP","id":"rs1484725205","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs60480853","source":"dbSNP","start":140538520,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140538520,"alleles":["T","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796529032","source":"dbSNP","start":140538525,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140538525,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1292230226","clinical_significance":[],"start":140538526,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140538526,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538528,"feature_type":"variation","strand":1,"end":140538528,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1796529201"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538529,"source":"dbSNP","strand":1,"feature_type":"variation","end":140538529,"alleles":["T","C"],"seq_region_name":"7","id":"rs1796529286","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1455208388","alleles":["C","T"],"end":140538535,"feature_type":"variation","strand":1,"source":"dbSNP","start":140538535,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1395247617","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538535,"feature_type":"variation","strand":1,"alleles":["CTCACTC","CTC"],"end":140538541},{"end":140538536,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140538536,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1171152983","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs954417578","end":140538538,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140538538,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1796529765","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140538539,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538539},{"alleles":["C","G"],"end":140538541,"feature_type":"variation","strand":1,"source":"dbSNP","start":140538541,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs2130502577","seq_region_name":"7"},{"end":140538542,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140538542,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1394445182","clinical_significance":[]},{"id":"rs1304203652","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538543,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140538543},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538546,"source":"dbSNP","strand":1,"feature_type":"variation","end":140538546,"alleles":["G","A","C"],"id":"rs1796530187","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796530332","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538549,"source":"dbSNP","strand":1,"feature_type":"variation","end":140538549,"alleles":["C","A","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796530511","feature_type":"variation","strand":1,"end":140538550,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538550},{"seq_region_name":"7","id":"rs985772777","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140538551,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538551,"source":"dbSNP"},{"source":"dbSNP","start":140538553,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140538553,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs933491616"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538557,"feature_type":"variation","strand":1,"end":140538557,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1796530992"},{"source":"dbSNP","start":140538559,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140538559,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796531133"},{"clinical_significance":[],"seq_region_name":"7","id":"rs186100087","source":"dbSNP","start":140538560,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140538560,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538564,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140538564,"seq_region_name":"7","id":"rs137910020","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140538565,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538565,"clinical_significance":[],"id":"rs947655135","seq_region_name":"7"},{"alleles":["G","A","T"],"end":140538568,"strand":1,"feature_type":"variation","start":140538568,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs149485737","clinical_significance":[]},{"start":140538573,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140538573,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796532006","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538577,"source":"dbSNP","strand":1,"feature_type":"variation","end":140538577,"alleles":["G","T"],"seq_region_name":"7","id":"rs1796532149","clinical_significance":[]},{"alleles":["C","T"],"end":140538585,"strand":1,"feature_type":"variation","start":140538585,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130502741","clinical_significance":[]},{"alleles":["A","C"],"end":140538587,"feature_type":"variation","strand":1,"source":"dbSNP","start":140538587,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585577826"},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140538588,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538588,"clinical_significance":[],"seq_region_name":"7","id":"rs1796532478"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538590,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140538590,"clinical_significance":[],"seq_region_name":"7","id":"rs902836535"},{"clinical_significance":[],"id":"rs534260545","seq_region_name":"7","alleles":["C","T"],"end":140538592,"feature_type":"variation","strand":1,"source":"dbSNP","start":140538592,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","G","T"],"end":140538594,"strand":1,"feature_type":"variation","start":140538594,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796532780","clinical_significance":[]},{"start":140538597,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140538597,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1443238906","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1425006561","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140538598,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538598},{"alleles":["G","A","T"],"end":140538602,"feature_type":"variation","strand":1,"source":"dbSNP","start":140538602,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1181135959"},{"seq_region_name":"7","id":"rs532684211","clinical_significance":[],"alleles":["T","C"],"end":140538604,"strand":1,"feature_type":"variation","start":140538604,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1270036239","source":"dbSNP","start":140538605,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140538605,"alleles":["T","C"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140538607,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538607,"source":"dbSNP","seq_region_name":"7","id":"rs1796533716","clinical_significance":[]},{"clinical_significance":[],"id":"rs1192323359","seq_region_name":"7","source":"dbSNP","start":140538608,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140538608,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140538609,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140538609,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1468477626","seq_region_name":"7"},{"end":140538616,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140538616,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs945237290","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140538617,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538617,"source":"dbSNP","seq_region_name":"7","id":"rs1211024141","clinical_significance":[]},{"source":"dbSNP","start":140538618,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140538618,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796534406"},{"id":"rs1796534495","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538619,"source":"dbSNP","strand":1,"feature_type":"variation","end":140538619,"alleles":["G","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538623,"source":"dbSNP","strand":1,"feature_type":"variation","end":140538623,"alleles":["C","T"],"seq_region_name":"7","id":"rs1352352358","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140538632,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538632,"source":"dbSNP","seq_region_name":"7","id":"rs1301303675","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796534770","clinical_significance":[],"alleles":["AA","AAA"],"end":140538633,"strand":1,"feature_type":"variation","start":140538632,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538633,"feature_type":"variation","strand":1,"end":140538633,"alleles":["A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1796534880"},{"seq_region_name":"7","id":"rs2130502911","clinical_significance":[],"alleles":["G","C"],"end":140538634,"strand":1,"feature_type":"variation","start":140538634,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538635,"source":"dbSNP","strand":1,"feature_type":"variation","end":140538635,"alleles":["T","C"],"id":"rs1347859320","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140538638,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538638,"clinical_significance":[],"seq_region_name":"7","id":"rs550785482"},{"seq_region_name":"7","id":"rs1286872050","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538640,"source":"dbSNP","strand":1,"feature_type":"variation","end":140538640,"alleles":["G","A"]},{"source":"dbSNP","start":140538647,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140538647,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1056827851"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796535675","end":140538651,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140538651,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs749379477","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140538652,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538652},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538653,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140538653,"seq_region_name":"7","id":"rs1253271172","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1469506905","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538654,"feature_type":"variation","strand":1,"end":140538654,"alleles":["C","A","G"]},{"source":"dbSNP","start":140538655,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140538655,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs569269948"},{"seq_region_name":"7","id":"rs1251819579","clinical_significance":[],"end":140538656,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140538656,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140538657,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140538657,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1796536343","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1466566057","clinical_significance":[],"end":140538660,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140538660,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140538663,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538663,"clinical_significance":[],"id":"rs1470510133","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1022748608","seq_region_name":"7","source":"dbSNP","start":140538667,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140538667,"alleles":["C","T"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140538668,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538668,"source":"dbSNP","id":"rs937894346","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796536749","clinical_significance":[],"alleles":["T","C"],"end":140538670,"strand":1,"feature_type":"variation","start":140538670,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140538671,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140538671,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796536849","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538672,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140538672,"clinical_significance":[],"seq_region_name":"7","id":"rs952779694"},{"alleles":["T","C"],"end":140538677,"strand":1,"feature_type":"variation","start":140538677,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1160230662","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538680,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140538680,"clinical_significance":[],"seq_region_name":"7","id":"rs2130503082"},{"seq_region_name":"7","id":"rs1796537140","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538681,"source":"dbSNP","strand":1,"feature_type":"variation","end":140538681,"alleles":["T","A"]},{"seq_region_name":"7","id":"rs1796537228","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538682,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140538682},{"start":140538685,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140538685,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796537320","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130503124","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538686,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140538686},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130503134","alleles":["A","G"],"end":140538687,"feature_type":"variation","strand":1,"source":"dbSNP","start":140538687,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140538688,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140538688,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs549222488","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140538689,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538689,"clinical_significance":[],"seq_region_name":"7","id":"rs2130503150"},{"source":"dbSNP","start":140538692,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140538692,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796537542"},{"strand":1,"feature_type":"variation","end":140538694,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538694,"source":"dbSNP","id":"rs1399919329","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1016705073","source":"dbSNP","start":140538695,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140538695,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs888449277","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538698,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140538698},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538705,"source":"dbSNP","strand":1,"feature_type":"variation","end":140538705,"alleles":["C","A"],"seq_region_name":"7","id":"rs1005676289","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538707,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140538707,"clinical_significance":[],"seq_region_name":"7","id":"rs1796538046"},{"feature_type":"variation","strand":1,"end":140538712,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538712,"clinical_significance":[],"seq_region_name":"7","id":"rs1796538201"},{"alleles":["G","A"],"end":140538717,"feature_type":"variation","strand":1,"source":"dbSNP","start":140538717,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs536231778"},{"seq_region_name":"7","id":"rs1483412996","clinical_significance":[],"strand":1,"feature_type":"variation","end":140538718,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538718,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140538720,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538720,"clinical_significance":[],"seq_region_name":"7","id":"rs1796538665"},{"start":140538723,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140538723,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1281826907","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1443354735","feature_type":"variation","strand":1,"end":140538725,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538725},{"seq_region_name":"7","id":"rs1347025048","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538731,"source":"dbSNP","strand":1,"feature_type":"variation","end":140538731,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs374706926","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538735,"source":"dbSNP","strand":1,"feature_type":"variation","end":140538735,"alleles":["A","G"]},{"id":"rs1229276319","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140538736,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538736,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1796539564","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538737,"feature_type":"variation","strand":1,"end":140538737,"alleles":["C","G"]},{"feature_type":"variation","strand":1,"end":140538743,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538743,"clinical_significance":[],"seq_region_name":"7","id":"rs191346806"},{"end":140538744,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140538744,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs775863145","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796540037","feature_type":"variation","strand":1,"end":140538746,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538746},{"strand":1,"feature_type":"variation","end":140538748,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538748,"source":"dbSNP","seq_region_name":"7","id":"rs1796540148","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140538750,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538750,"source":"dbSNP","seq_region_name":"7","id":"rs923351983","clinical_significance":[]},{"seq_region_name":"7","id":"rs1396813701","clinical_significance":[],"start":140538754,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G","T"],"end":140538754,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1796540511","clinical_significance":[],"end":140538761,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140538761,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1377550481","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538764,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140538764},{"seq_region_name":"7","id":"rs1796540691","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538769,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140538769},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538775,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140538775,"clinical_significance":[],"seq_region_name":"7","id":"rs1223618757"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1434216532","end":140538780,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140538780,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs541797099","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538783,"source":"dbSNP","strand":1,"feature_type":"variation","end":140538785,"alleles":["GGG","GG"]},{"start":140538784,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140538784,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs181101075","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130503388","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140538785,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538785,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140538787,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538787,"source":"dbSNP","seq_region_name":"7","id":"rs1336568939","clinical_significance":[]},{"seq_region_name":"7","id":"rs1372859173","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538788,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140538788},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538790,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140538790,"seq_region_name":"7","id":"rs1188755304","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130503419","clinical_significance":[],"start":140538791,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140538791,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1442621987","seq_region_name":"7","source":"dbSNP","start":140538795,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140538795,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796541561","feature_type":"variation","strand":1,"end":140538800,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538800},{"end":140538801,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140538801,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs567719331","clinical_significance":[]},{"start":140538803,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140538803,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1208054120","clinical_significance":[]},{"end":140538812,"alleles":["TTTTTT","TTTTT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140538807,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1563125054"},{"seq_region_name":"7","id":"rs2130503461","clinical_significance":[],"alleles":["T","A"],"end":140538811,"strand":1,"feature_type":"variation","start":140538811,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs910718225","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538812,"source":"dbSNP","strand":1,"feature_type":"variation","end":140538812,"alleles":["T","A"]},{"seq_region_name":"7","id":"rs947656948","clinical_significance":[],"alleles":["A","T"],"end":140538813,"strand":1,"feature_type":"variation","start":140538813,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1272072897","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538813,"feature_type":"variation","strand":1,"alleles":["AAAAAA","AAAAA"],"end":140538818},{"seq_region_name":"7","id":"rs1017262966","clinical_significance":[],"strand":1,"feature_type":"variation","end":140538817,"alleles":["A","C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538817,"source":"dbSNP"},{"alleles":["A","T"],"end":140538818,"feature_type":"variation","strand":1,"source":"dbSNP","start":140538818,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs115892192"},{"alleles":["T","A","C"],"end":140538819,"strand":1,"feature_type":"variation","start":140538819,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs185534287","clinical_significance":[]},{"source":"dbSNP","start":140538822,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TTTCTTTCTTT","TTTCTTT"],"end":140538832,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1291689856"},{"end":140538826,"alleles":["TCT","T"],"strand":1,"feature_type":"variation","start":140538824,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796542645","clinical_significance":[]},{"clinical_significance":[],"id":"rs2130503538","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538825,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140538825},{"id":"rs768743987","seq_region_name":"7","clinical_significance":[],"end":140538826,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140538826,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1405225783","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140538827,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538827,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585578448","feature_type":"variation","strand":1,"end":140538828,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538828},{"id":"rs556757454","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538829,"source":"dbSNP","strand":1,"feature_type":"variation","end":140538829,"alleles":["C","A"]},{"id":"rs913652121","seq_region_name":"7","clinical_significance":[],"start":140538834,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140538841,"alleles":["TTTTTTTT","TTTTTTTTT"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140538835,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538835,"clinical_significance":[],"seq_region_name":"7","id":"rs934331195"},{"seq_region_name":"7","id":"rs1331047912","clinical_significance":[],"strand":1,"feature_type":"variation","end":140538836,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538836,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538837,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140538837,"seq_region_name":"7","id":"rs1188456009","clinical_significance":[]},{"alleles":["T","C","G"],"end":140538839,"feature_type":"variation","strand":1,"source":"dbSNP","start":140538839,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130503599"},{"seq_region_name":"7","id":"rs2130503615","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538840,"source":"dbSNP","strand":1,"feature_type":"variation","end":140538840,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1396479046","clinical_significance":[],"start":140538842,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140538842,"strand":1,"feature_type":"variation"},{"id":"rs1164171418","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140538843,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538843,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1473998924","seq_region_name":"7","source":"dbSNP","start":140538844,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140538844,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1419508848","source":"dbSNP","start":140538847,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AGAG","AG"],"end":140538850,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1796543812","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538849,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140538849},{"seq_region_name":"7","id":"rs1419749784","clinical_significance":[],"end":140538852,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140538852,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs190342187","clinical_significance":[],"strand":1,"feature_type":"variation","end":140538854,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538854,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1163064838","alleles":["G","A","T"],"end":140538855,"feature_type":"variation","strand":1,"source":"dbSNP","start":140538855,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140538858,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140538858,"alleles":["C","G"],"strand":1,"feature_type":"variation","id":"rs981977344","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585578620","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140538861,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538861},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538867,"source":"dbSNP","strand":1,"feature_type":"variation","end":140538867,"alleles":["A","C"],"id":"rs1435975081","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1796544499","seq_region_name":"7","feature_type":"variation","strand":1,"end":140538869,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538869},{"clinical_significance":[],"seq_region_name":"7","id":"rs575416376","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538870,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140538870},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140538873,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538873,"source":"dbSNP","seq_region_name":"7","id":"rs1410631606","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796544779","alleles":["C","T"],"end":140538878,"feature_type":"variation","strand":1,"source":"dbSNP","start":140538878,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","A"],"end":140538886,"feature_type":"variation","strand":1,"source":"dbSNP","start":140538886,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796544873"},{"alleles":["A","G"],"end":140538888,"strand":1,"feature_type":"variation","start":140538888,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1796544953","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140538889,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538889,"clinical_significance":[],"seq_region_name":"7","id":"rs1796545058"},{"end":140538892,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140538892,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs182899473"},{"feature_type":"variation","strand":1,"end":140538894,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538894,"clinical_significance":[],"id":"rs1210163359","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1336683957","seq_region_name":"7","feature_type":"variation","strand":1,"end":140538899,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538899},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796545434","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538904,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140538904},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140538905,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538905,"source":"dbSNP","seq_region_name":"7","id":"rs895605614","clinical_significance":[]},{"id":"rs1796545611","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140538914,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538914,"source":"dbSNP"},{"alleles":["T","G"],"end":140538916,"feature_type":"variation","strand":1,"source":"dbSNP","start":140538916,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1232891156"},{"seq_region_name":"7","id":"rs535051446","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140538922,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538922,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538924,"feature_type":"variation","strand":1,"end":140538924,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1441584426"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538926,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140538926,"clinical_significance":[],"seq_region_name":"7","id":"rs560855660"},{"source":"dbSNP","start":140538928,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G","T"],"end":140538928,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1357600608"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1440167779","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538931,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140538931},{"source":"dbSNP","start":140538936,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140538936,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1231750737"},{"seq_region_name":"7","id":"rs1292423588","clinical_significance":[],"start":140538937,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140538937,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538943,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140538943,"seq_region_name":"7","id":"rs763568413","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538943,"feature_type":"variation","strand":1,"end":140538944,"alleles":["CC","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1339876872"},{"seq_region_name":"7","id":"rs1563125155","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538946,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140538946},{"id":"rs2130503909","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140538947,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538947,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538949,"feature_type":"variation","strand":1,"end":140538949,"alleles":["G","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585578846"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538951,"feature_type":"variation","strand":1,"end":140538951,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1164743910"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140538952,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538952,"clinical_significance":[],"seq_region_name":"7","id":"rs1796546994"},{"seq_region_name":"7","id":"rs1460583018","clinical_significance":[],"start":140538953,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140538953,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140538959,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538959,"clinical_significance":[],"seq_region_name":"7","id":"rs1408314188"},{"id":"rs1270820741","seq_region_name":"7","clinical_significance":[],"alleles":["A","G"],"end":140538963,"strand":1,"feature_type":"variation","start":140538963,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538964,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140538964,"clinical_significance":[],"id":"rs1796547693","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1055041479","alleles":["G","A"],"end":140538967,"feature_type":"variation","strand":1,"source":"dbSNP","start":140538967,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1468176159","end":140538968,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140538968,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs62485803","seq_region_name":"7","clinical_significance":[],"end":140538969,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140538969,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1796548328","clinical_significance":[],"start":140538970,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140538970,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140538972,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140538972,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796548433"},{"seq_region_name":"7","id":"rs1796548563","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538973,"source":"dbSNP","strand":1,"feature_type":"variation","end":140538973,"alleles":["G","C"]},{"source":"dbSNP","start":140538979,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140538979,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796548703"},{"start":140538980,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140538980,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1044234483","clinical_significance":[]},{"id":"rs1474010916","seq_region_name":"7","clinical_significance":[],"end":140538981,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140538981,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1796549230","clinical_significance":[],"strand":1,"feature_type":"variation","end":140538982,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140538982,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1250890569","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538985,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140538985},{"source":"dbSNP","start":140538986,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140538986,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs572754723"},{"end":140538989,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140538989,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1330054019","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1286654952","feature_type":"variation","strand":1,"end":140538998,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140538998},{"end":140539003,"alleles":["TTTTT","TTTT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140538999,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1563125197"},{"alleles":["T","C"],"end":140539001,"feature_type":"variation","strand":1,"source":"dbSNP","start":140539001,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1222099854","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140539003,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539003,"clinical_significance":[],"id":"rs1796550207","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140539004,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539004,"clinical_significance":[],"seq_region_name":"7","id":"rs1350062452"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1275891380","end":140539005,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140539005,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["A","G"],"end":140539007,"strand":1,"feature_type":"variation","start":140539007,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1443746550","clinical_significance":[]},{"id":"rs1796550777","seq_region_name":"7","clinical_significance":[],"start":140539009,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C","G"],"end":140539009,"strand":1,"feature_type":"variation"},{"alleles":["A","G"],"end":140539013,"strand":1,"feature_type":"variation","start":140539013,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1368219484","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","A"],"end":140539014,"feature_type":"variation","strand":1,"source":"dbSNP","start":140539014,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1796551085","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539015,"source":"dbSNP","strand":1,"feature_type":"variation","end":140539015,"alleles":["G","A"],"seq_region_name":"7","id":"rs556792265","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140539020,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539020,"source":"dbSNP","seq_region_name":"7","id":"rs575335170","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1436316915","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140539022,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539022},{"clinical_significance":[],"id":"rs1796551615","seq_region_name":"7","end":140539024,"alleles":["A","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140539024,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539025,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140539025,"clinical_significance":[],"id":"rs1345365146","seq_region_name":"7"},{"seq_region_name":"7","id":"rs540133365","clinical_significance":[],"start":140539026,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140539026,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140539034,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140539039,"alleles":["GGCTGG","GG"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1160857177"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796552075","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539040,"feature_type":"variation","strand":1,"end":140539040,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1475959992","clinical_significance":[],"start":140539042,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140539042,"strand":1,"feature_type":"variation"},{"start":140539043,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140539043,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs565127496","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1394975210","alleles":["G","C","T"],"end":140539044,"feature_type":"variation","strand":1,"source":"dbSNP","start":140539044,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539046,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140539046,"seq_region_name":"7","id":"rs897023246","clinical_significance":[]},{"id":"rs941345985","seq_region_name":"7","clinical_significance":[],"start":140539047,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140539047,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1796553028","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539049,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140539049},{"clinical_significance":[],"seq_region_name":"7","id":"rs1229175418","source":"dbSNP","start":140539050,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140539050,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1393240175","end":140539051,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140539051,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539052,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140539052,"clinical_significance":[],"seq_region_name":"7","id":"rs993504278"},{"source":"dbSNP","start":140539053,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140539053,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796553588"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1192735521","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539054,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140539054},{"clinical_significance":[],"seq_region_name":"7","id":"rs532190697","end":140539055,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140539055,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539057,"feature_type":"variation","strand":1,"end":140539057,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130504342"},{"seq_region_name":"7","id":"rs1486087008","clinical_significance":[],"start":140539060,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140539060,"strand":1,"feature_type":"variation"},{"alleles":["C","G"],"end":140539061,"strand":1,"feature_type":"variation","start":140539061,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1244007534","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539063,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140539063,"seq_region_name":"7","id":"rs1213916126","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796554180","clinical_significance":[],"strand":1,"feature_type":"variation","end":140539066,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539066,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1796554321","clinical_significance":[],"strand":1,"feature_type":"variation","end":140539068,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539068,"source":"dbSNP"},{"id":"rs539140754","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140539069,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539069,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs557981267","alleles":["G","A"],"end":140539070,"feature_type":"variation","strand":1,"source":"dbSNP","start":140539070,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140539072,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539072,"clinical_significance":[],"seq_region_name":"7","id":"rs1413128413"},{"id":"rs1236656887","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539073,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140539073},{"feature_type":"variation","strand":1,"end":140539078,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539078,"clinical_significance":[],"seq_region_name":"7","id":"rs1796555073"},{"id":"rs1563125299","seq_region_name":"7","clinical_significance":[],"start":140539081,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["CCC","CC"],"end":140539083,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs986195577","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539082,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140539082},{"feature_type":"variation","strand":1,"end":140539083,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539083,"clinical_significance":[],"id":"rs1018077104","seq_region_name":"7"},{"source":"dbSNP","start":140539084,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140539084,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs61408713","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs968932824","end":140539090,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140539090,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["T","C"],"end":140539091,"strand":1,"feature_type":"variation","start":140539091,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1333790332","clinical_significance":[]},{"id":"rs1796556025","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140539092,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539092,"source":"dbSNP"},{"alleles":["G","C"],"end":140539093,"strand":1,"feature_type":"variation","start":140539093,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1796556123","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1303341425","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140539094,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539094,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585579308","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539101,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140539101},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585579318","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539103,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140539103},{"seq_region_name":"7","id":"rs562814320","clinical_significance":[],"start":140539104,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140539104,"strand":1,"feature_type":"variation"},{"start":140539106,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140539106,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs924897832","clinical_significance":[]},{"source":"dbSNP","start":140539109,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140539109,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1287551440"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539110,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140539110,"seq_region_name":"7","id":"rs1796556729","clinical_significance":[]},{"source":"dbSNP","start":140539112,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140539112,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1229354807"},{"alleles":["C","G","T"],"end":140539115,"feature_type":"variation","strand":1,"source":"dbSNP","start":140539115,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs75737822"},{"seq_region_name":"7","id":"rs573067843","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539116,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140539116},{"source":"dbSNP","start":140539125,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140539125,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1436081621","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1393143550","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539128,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140539128},{"clinical_significance":[],"seq_region_name":"7","id":"rs916897254","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539129,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140539129},{"alleles":["T","G"],"end":140539142,"feature_type":"variation","strand":1,"source":"dbSNP","start":140539142,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1234996881"},{"end":140539143,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140539143,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796557918"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539149,"source":"dbSNP","strand":1,"feature_type":"variation","end":140539149,"alleles":["T","A"],"seq_region_name":"7","id":"rs2130504612","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130504617","clinical_significance":[],"end":140539153,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140539153,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs2130504626","clinical_significance":[],"strand":1,"feature_type":"variation","end":140539154,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539154,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1051296340","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539157,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140539157},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140539158,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539158,"source":"dbSNP","seq_region_name":"7","id":"rs1184623342","clinical_significance":[]},{"seq_region_name":"7","id":"rs1475196617","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539164,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140539164},{"alleles":["C","T"],"end":140539168,"strand":1,"feature_type":"variation","start":140539168,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130504669","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796558473","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140539170,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539170,"source":"dbSNP"},{"end":140539171,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140539171,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs565037359","seq_region_name":"7","clinical_significance":[]},{"start":140539173,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140539173,"alleles":["G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs546014533","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1213050142","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539176,"feature_type":"variation","strand":1,"end":140539176,"alleles":["C","T"]},{"end":140539179,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140539179,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796559061"},{"clinical_significance":[],"seq_region_name":"7","id":"rs144031980","feature_type":"variation","strand":1,"end":140539183,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539183},{"start":140539184,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140539184,"alleles":["C","A"],"strand":1,"feature_type":"variation","id":"rs74459160","seq_region_name":"7","clinical_significance":[]},{"end":140539185,"alleles":["C","A","G"],"strand":1,"feature_type":"variation","start":140539185,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1206486897","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796559588","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539187,"source":"dbSNP","strand":1,"feature_type":"variation","end":140539187,"alleles":["T","G"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539188,"source":"dbSNP","strand":1,"feature_type":"variation","end":140539188,"alleles":["G","A","C"],"seq_region_name":"7","id":"rs1309839590","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140539189,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539189,"clinical_significance":[],"id":"rs1796559862","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539192,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140539192,"clinical_significance":[],"seq_region_name":"7","id":"rs1262011229"},{"feature_type":"variation","strand":1,"end":140539196,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539196,"clinical_significance":[],"seq_region_name":"7","id":"rs759991491"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539200,"feature_type":"variation","strand":1,"end":140539200,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1447875509"},{"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140539203,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539203,"clinical_significance":[],"id":"rs888168449","seq_region_name":"7"},{"alleles":["C","T"],"end":140539205,"strand":1,"feature_type":"variation","start":140539205,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs941204493","clinical_significance":[]},{"seq_region_name":"7","id":"rs79981964","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140539209,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539209,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539214,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140539214,"seq_region_name":"7","id":"rs767309003","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140539222,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539222,"clinical_significance":[],"id":"rs1174861619","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585579573","alleles":["A","T"],"end":140539232,"feature_type":"variation","strand":1,"source":"dbSNP","start":140539232,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539233,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140539233,"clinical_significance":[],"seq_region_name":"7","id":"rs1585579583"},{"id":"rs2130504862","seq_region_name":"7","clinical_significance":[],"start":140539234,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140539234,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796561349","feature_type":"variation","strand":1,"end":140539235,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539235},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130504883","source":"dbSNP","start":140539236,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140539236,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1396922790","source":"dbSNP","start":140539237,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140539237,"alleles":["C","T"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140539241,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539241,"source":"dbSNP","seq_region_name":"7","id":"rs1563125407","clinical_significance":[]},{"seq_region_name":"7","id":"rs1311822655","clinical_significance":[],"end":140539244,"alleles":["AAA","AA"],"strand":1,"feature_type":"variation","start":140539242,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140539244,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539244,"clinical_significance":[],"id":"rs1432963210","seq_region_name":"7"},{"clinical_significance":[],"id":"rs750047797","seq_region_name":"7","feature_type":"variation","strand":1,"end":140539246,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539246},{"alleles":["A","T"],"end":140539247,"strand":1,"feature_type":"variation","start":140539247,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs752995537","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796562474","source":"dbSNP","start":140539252,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140539252,"alleles":["G","A"],"feature_type":"variation","strand":1},{"start":140539255,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140539255,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1462425250","clinical_significance":[]},{"seq_region_name":"7","id":"rs376303585","clinical_significance":[],"end":140539256,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140539256,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["G","A"],"end":140539258,"strand":1,"feature_type":"variation","start":140539258,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796562963","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1168023784","end":140539259,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140539259,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140539263,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140539263,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1563125430","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140539264,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539264,"source":"dbSNP","seq_region_name":"7","id":"rs1796563338","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140539266,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539266,"clinical_significance":[],"seq_region_name":"7","id":"rs1030360514"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1418770930","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539267,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140539267},{"id":"rs148677523","seq_region_name":"7","clinical_significance":[],"end":140539270,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140539270,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs571061376","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140539271,"strand":1,"feature_type":"variation","start":140539271,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1474385243","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539273,"feature_type":"variation","strand":1,"end":140539273,"alleles":["T","C"]},{"id":"rs1256882523","seq_region_name":"7","clinical_significance":[],"start":140539276,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140539276,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140539281,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539281,"source":"dbSNP","seq_region_name":"7","id":"rs1177902017","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539283,"feature_type":"variation","strand":1,"end":140539283,"alleles":["C","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs959201753"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1007541871","source":"dbSNP","start":140539291,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140539291,"alleles":["G","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1250157795","clinical_significance":[],"start":140539294,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140539294,"alleles":["A","AA"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140539297,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140539297,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796564987"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796565112","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539308,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140539308},{"id":"rs990616432","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539311,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140539311},{"seq_region_name":"7","id":"rs1384197164","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140539313,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539313,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539314,"feature_type":"variation","strand":1,"end":140539314,"alleles":["G","T"],"clinical_significance":[],"id":"rs1563125465","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1796565738","seq_region_name":"7","alleles":["C","A"],"end":140539318,"feature_type":"variation","strand":1,"source":"dbSNP","start":140539318,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1017692642","source":"dbSNP","start":140539322,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140539322,"feature_type":"variation","strand":1},{"alleles":["GGGGG","GGGG","GGGGGG"],"end":140539326,"feature_type":"variation","strand":1,"source":"dbSNP","start":140539322,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs909821281"},{"alleles":["G","T"],"end":140539323,"strand":1,"feature_type":"variation","start":140539323,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796566225","clinical_significance":[]},{"seq_region_name":"7","id":"rs1234748429","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539331,"source":"dbSNP","strand":1,"feature_type":"variation","end":140539331,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796566473","source":"dbSNP","start":140539333,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140539333,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796566613","end":140539335,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140539335,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1353245034","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140539337,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539337},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140539338,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539338,"source":"dbSNP","seq_region_name":"7","id":"rs1796566868","clinical_significance":[]},{"source":"dbSNP","start":140539339,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140539339,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs778040517"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1391506564","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539345,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140539345},{"start":140539347,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140539347,"strand":1,"feature_type":"variation","id":"rs978988661","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539350,"source":"dbSNP","strand":1,"feature_type":"variation","end":140539350,"alleles":["T","C"],"id":"rs1796567217","seq_region_name":"7","clinical_significance":[]},{"end":140539351,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140539351,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796567333","clinical_significance":[]},{"id":"rs1796567427","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140539354,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539354,"source":"dbSNP"},{"source":"dbSNP","start":140539356,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140539356,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1375375044"},{"clinical_significance":[],"id":"rs201526783","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539361,"feature_type":"variation","strand":1,"end":140539361,"alleles":["T","A"]},{"source":"dbSNP","start":140539362,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140539362,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796567684"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539365,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140539365,"clinical_significance":[],"seq_region_name":"7","id":"rs1461234555"},{"seq_region_name":"7","id":"rs1796567865","clinical_significance":[],"start":140539366,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140539367,"alleles":["GG","G"],"strand":1,"feature_type":"variation"},{"start":140539370,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140539370,"alleles":["A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585579864","clinical_significance":[]},{"seq_region_name":"7","id":"rs1394933024","clinical_significance":[],"end":140539373,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140539373,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1364248119","seq_region_name":"7","end":140539377,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140539377,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140539387,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539387,"source":"dbSNP","id":"rs1037064460","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs141328770","source":"dbSNP","start":140539388,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140539388,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539390,"feature_type":"variation","strand":1,"end":140539390,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs934131759"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563125517","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539391,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140539391},{"seq_region_name":"7","id":"rs1051606657","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140539393,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539393,"source":"dbSNP"},{"seq_region_name":"7","id":"rs889833307","clinical_significance":[],"start":140539397,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140539397,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539398,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140539398,"id":"rs2130505338","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539399,"source":"dbSNP","strand":1,"feature_type":"variation","end":140539399,"alleles":["T","C"],"seq_region_name":"7","id":"rs1248965596","clinical_significance":[]},{"start":140539403,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140539403,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs147440749","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539404,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140539404,"clinical_significance":[],"id":"rs1796569091","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140539405,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539405,"clinical_significance":[],"seq_region_name":"7","id":"rs1796569183"},{"clinical_significance":[],"id":"rs1469358987","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539410,"feature_type":"variation","strand":1,"end":140539410,"alleles":["G","T"]},{"clinical_significance":[],"id":"rs1260874623","seq_region_name":"7","source":"dbSNP","start":140539420,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140539420,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs956316557","end":140539422,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140539422,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1796569538","clinical_significance":[],"strand":1,"feature_type":"variation","end":140539425,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539425,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1796569636","seq_region_name":"7","alleles":["G","-"],"end":140539426,"feature_type":"variation","strand":1,"source":"dbSNP","start":140539426,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1796569722","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140539428,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539428,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140539429,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539429,"clinical_significance":[],"seq_region_name":"7","id":"rs1796569813"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539437,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140539437,"clinical_significance":[],"id":"rs1212267141","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796570085","alleles":["G","A"],"end":140539443,"feature_type":"variation","strand":1,"source":"dbSNP","start":140539443,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140539445,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140539445,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796570231"},{"alleles":["A","T"],"end":140539450,"feature_type":"variation","strand":1,"source":"dbSNP","start":140539450,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1332180125"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1264526011","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539451,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140539451},{"id":"rs1796570702","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140539453,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539453,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140539456,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539456,"clinical_significance":[],"id":"rs993029585","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539457,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140539457,"clinical_significance":[],"seq_region_name":"7","id":"rs1054527205"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539459,"feature_type":"variation","strand":1,"end":140539459,"alleles":["G","A"],"clinical_significance":[],"id":"rs893400183","seq_region_name":"7"},{"end":140539460,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140539460,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585580024"},{"alleles":["A","C"],"end":140539465,"strand":1,"feature_type":"variation","start":140539465,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1796571469","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140539466,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539466,"clinical_significance":[],"id":"rs757325481","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140539467,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539467,"source":"dbSNP","seq_region_name":"7","id":"rs1796571785","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796571930","clinical_significance":[],"start":140539468,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140539468,"strand":1,"feature_type":"variation"},{"id":"rs1796572074","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539469,"source":"dbSNP","strand":1,"feature_type":"variation","end":140539469,"alleles":["C","T"]},{"alleles":["C","T"],"end":140539470,"strand":1,"feature_type":"variation","start":140539470,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796572222","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs566759204","feature_type":"variation","strand":1,"end":140539471,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539471},{"source":"dbSNP","start":140539472,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140539472,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs902171665","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1327632641","clinical_significance":[],"start":140539473,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140539473,"alleles":["T","G"],"strand":1,"feature_type":"variation"},{"alleles":["G","A"],"end":140539478,"strand":1,"feature_type":"variation","start":140539478,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130505592","clinical_significance":[]},{"id":"rs1194752256","seq_region_name":"7","clinical_significance":[],"start":140539482,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C","T"],"end":140539482,"strand":1,"feature_type":"variation"},{"start":140539486,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140539486,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs540544007","clinical_significance":[]},{"seq_region_name":"7","id":"rs1452583697","clinical_significance":[],"start":140539487,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140539487,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539493,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140539493,"clinical_significance":[],"id":"rs1563125569","seq_region_name":"7"},{"clinical_significance":[],"id":"rs969712286","seq_region_name":"7","alleles":["A","C"],"end":140539496,"feature_type":"variation","strand":1,"source":"dbSNP","start":140539496,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1175441017","clinical_significance":[],"start":140539501,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140539501,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539502,"source":"dbSNP","strand":1,"feature_type":"variation","end":140539502,"alleles":["G","T"],"seq_region_name":"7","id":"rs980134801","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140539503,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539503,"source":"dbSNP","seq_region_name":"7","id":"rs1796573353","clinical_significance":[]},{"seq_region_name":"7","id":"rs4458784","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140539505,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539505,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140539507,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539507,"source":"dbSNP","seq_region_name":"7","id":"rs941099247","clinical_significance":[]},{"seq_region_name":"7","id":"rs1035187707","clinical_significance":[],"end":140539508,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140539508,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539511,"feature_type":"variation","strand":1,"end":140539511,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1796574021"},{"alleles":["G","A"],"end":140539513,"strand":1,"feature_type":"variation","start":140539513,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1036905741","clinical_significance":[]},{"start":140539519,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140539519,"alleles":["C","G"],"strand":1,"feature_type":"variation","id":"rs1455516875","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs959089527","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539523,"source":"dbSNP","strand":1,"feature_type":"variation","end":140539523,"alleles":["C","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539525,"feature_type":"variation","strand":1,"end":140539525,"alleles":["C","G"],"clinical_significance":[],"id":"rs1563125594","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs535847471","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539531,"feature_type":"variation","strand":1,"end":140539531,"alleles":["T","C"]},{"alleles":["C","T"],"end":140539533,"strand":1,"feature_type":"variation","start":140539533,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1397476758","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796575001","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140539534,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539534,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1192101714","end":140539538,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140539538,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["A","G"],"end":140539539,"strand":1,"feature_type":"variation","start":140539539,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796575246","clinical_significance":[]},{"alleles":["C","T"],"end":140539540,"strand":1,"feature_type":"variation","start":140539540,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs990665627","clinical_significance":[]},{"source":"dbSNP","start":140539542,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140539542,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1266145130"},{"clinical_significance":[],"id":"rs1205345498","seq_region_name":"7","feature_type":"variation","strand":1,"end":140539546,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539546},{"clinical_significance":[],"seq_region_name":"7","id":"rs187380033","source":"dbSNP","start":140539547,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140539547,"alleles":["G","A"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140539548,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140539548,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs866863731"},{"strand":1,"feature_type":"variation","end":140539549,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539549,"source":"dbSNP","id":"rs1238843644","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs962643870","source":"dbSNP","start":140539551,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140539551,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1051027673","alleles":["C","A"],"end":140539552,"feature_type":"variation","strand":1,"source":"dbSNP","start":140539552,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130505829","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140539554,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539554},{"alleles":["C","T"],"end":140539555,"strand":1,"feature_type":"variation","start":140539555,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1231732598","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539557,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140539557,"clinical_significance":[],"seq_region_name":"7","id":"rs889668326"},{"seq_region_name":"7","id":"rs1796576526","clinical_significance":[],"start":140539562,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140539562,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"end":140539563,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140539563,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1007568185"},{"feature_type":"variation","strand":1,"end":140539571,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539571,"clinical_significance":[],"seq_region_name":"7","id":"rs745967419"},{"seq_region_name":"7","id":"rs1296113230","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["CC","C"],"end":140539572,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539571,"source":"dbSNP"},{"end":140539572,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140539572,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1039439520","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140539573,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539573,"clinical_significance":[],"seq_region_name":"7","id":"rs904646815"},{"seq_region_name":"7","id":"rs1796577410","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539586,"source":"dbSNP","strand":1,"feature_type":"variation","end":140539586,"alleles":["C","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1000672075","feature_type":"variation","strand":1,"end":140539588,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539588},{"source":"dbSNP","start":140539589,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140539589,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1172318028","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140539591,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539591,"clinical_significance":[],"seq_region_name":"7","id":"rs1796577889"},{"seq_region_name":"7","id":"rs1796577993","clinical_significance":[],"start":140539593,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140539593,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1796578090","clinical_significance":[],"strand":1,"feature_type":"variation","end":140539596,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539596,"source":"dbSNP"},{"alleles":["C","T"],"end":140539600,"feature_type":"variation","strand":1,"source":"dbSNP","start":140539600,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs942756623"},{"source":"dbSNP","start":140539603,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140539603,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130505920"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539604,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140539604,"seq_region_name":"7","id":"rs1796578385","clinical_significance":[]},{"alleles":["C","T"],"end":140539606,"feature_type":"variation","strand":1,"source":"dbSNP","start":140539606,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1236382474","seq_region_name":"7"},{"alleles":["T","G"],"end":140539611,"feature_type":"variation","strand":1,"source":"dbSNP","start":140539611,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs192067794"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1328842812","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539615,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140539615},{"feature_type":"variation","strand":1,"end":140539620,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539620,"clinical_significance":[],"seq_region_name":"7","id":"rs540169690"},{"seq_region_name":"7","id":"rs182738522","clinical_significance":[],"start":140539627,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140539627,"alleles":["C","A","T"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539628,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140539628,"clinical_significance":[],"id":"rs548960638","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796579497","alleles":["A","C"],"end":140539630,"feature_type":"variation","strand":1,"source":"dbSNP","start":140539630,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140539631,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539631,"source":"dbSNP","seq_region_name":"7","id":"rs1282298053","clinical_significance":[]},{"clinical_significance":[],"id":"rs1796579777","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539636,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140539636},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140539637,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539637,"clinical_significance":[],"seq_region_name":"7","id":"rs1208637714"},{"strand":1,"feature_type":"variation","end":140539638,"alleles":["C","A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539638,"source":"dbSNP","seq_region_name":"7","id":"rs1467513055","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796580211","clinical_significance":[],"start":140539640,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140539640,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1270532915","seq_region_name":"7","source":"dbSNP","start":140539641,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140539641,"alleles":["G","A"],"feature_type":"variation","strand":1},{"start":140539648,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140539648,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1229395031","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1324872054","feature_type":"variation","strand":1,"alleles":["A","T"],"end":140539652,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539652},{"strand":1,"feature_type":"variation","end":140539655,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539655,"source":"dbSNP","id":"rs1796580766","seq_region_name":"7","clinical_significance":[]},{"end":140539657,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140539657,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1277832389","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796581046","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539660,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140539660},{"start":140539662,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140539662,"strand":1,"feature_type":"variation","id":"rs1796581173","seq_region_name":"7","clinical_significance":[]},{"start":140539664,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140539664,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs970247861","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140539665,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539665,"source":"dbSNP","seq_region_name":"7","id":"rs1796581436","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539666,"feature_type":"variation","strand":1,"end":140539666,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1415400752"},{"source":"dbSNP","start":140539668,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140539668,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1357439733"},{"clinical_significance":[],"id":"rs576991824","seq_region_name":"7","source":"dbSNP","start":140539669,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140539669,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140539671,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140539671,"alleles":["A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796581953"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539671,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","-"],"end":140539671,"id":"rs1796582090","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","A","C"],"end":140539673,"feature_type":"variation","strand":1,"source":"dbSNP","start":140539673,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1414376589","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1563125699","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140539674,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539674,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130506165","source":"dbSNP","start":140539678,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140539678,"alleles":["A","G"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539679,"feature_type":"variation","strand":1,"end":140539679,"alleles":["T","A","C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs563807268"},{"clinical_significance":[],"id":"rs909535398","seq_region_name":"7","feature_type":"variation","strand":1,"end":140539687,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539687},{"source":"dbSNP","start":140539687,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140539711,"alleles":["CGCAGGTCAGACCCTCAGAAGGCGC","CGC"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1370925628"},{"clinical_significance":[],"seq_region_name":"7","id":"rs78670283","source":"dbSNP","start":140539688,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140539688,"alleles":["G","A","T"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539689,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140539689,"seq_region_name":"7","id":"rs1185224711","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796583861","end":140539690,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140539690,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140539692,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C","T"],"end":140539692,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs972881248","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796584211","source":"dbSNP","start":140539693,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140539693,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796584363","alleles":["G","C"],"end":140539696,"feature_type":"variation","strand":1,"source":"dbSNP","start":140539696,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs918316781","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140539702,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539702,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796584684","feature_type":"variation","strand":1,"alleles":["CAGA","-"],"end":140539705,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539702},{"seq_region_name":"7","id":"rs10952729","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539703,"source":"dbSNP","strand":1,"feature_type":"variation","end":140539703,"alleles":["A","C","G"]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140539707,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539707,"clinical_significance":[],"seq_region_name":"7","id":"rs769528249"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1257258387","end":140539709,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140539709,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs542342271","feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140539710,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539710},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539711,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140539711,"seq_region_name":"7","id":"rs1796585573","clinical_significance":[]},{"alleles":["CCC","CC"],"end":140539713,"feature_type":"variation","strand":1,"source":"dbSNP","start":140539711,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796585701"},{"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140539713,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539713,"clinical_significance":[],"seq_region_name":"7","id":"rs111437786"},{"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140539714,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539714,"clinical_significance":[],"seq_region_name":"7","id":"rs527672429"},{"end":140539717,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140539717,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1336819572","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796586431","clinical_significance":[],"strand":1,"feature_type":"variation","end":140539736,"alleles":["CAGAGGCCGCTCAGAGGCC","CAGAGGCCGCTCAGAGGCCGCTCAGAGGCC"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539718,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1796586585","seq_region_name":"7","feature_type":"variation","strand":1,"end":140539719,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539719},{"seq_region_name":"7","id":"rs1331473435","clinical_significance":[],"alleles":["G","A","T"],"end":140539722,"strand":1,"feature_type":"variation","start":140539722,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796586917","source":"dbSNP","start":140539723,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140539723,"alleles":["G","C"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140539724,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539724,"source":"dbSNP","seq_region_name":"7","id":"rs1389961604","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs111925526","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539725,"feature_type":"variation","strand":1,"end":140539725,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs187507780","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140539726,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539726},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796587372","feature_type":"variation","strand":1,"end":140539739,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539739},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539740,"feature_type":"variation","strand":1,"end":140539740,"alleles":["C","A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1298710133"},{"end":140539743,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140539743,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs904511473","clinical_significance":[]},{"id":"rs1025984494","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539744,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140539744},{"seq_region_name":"7","id":"rs1000174358","clinical_significance":[],"strand":1,"feature_type":"variation","end":140539748,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539748,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1183894513","clinical_significance":[],"strand":1,"feature_type":"variation","end":140539749,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539749,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140539751,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539751,"clinical_significance":[],"id":"rs10952730","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539752,"source":"dbSNP","strand":1,"feature_type":"variation","end":140539752,"alleles":["G","A"],"id":"rs1796588661","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1234808719","clinical_significance":[],"alleles":["CCGTCATCCTCATC","CCGTCATCCTCATCCGTCATCCTCATC"],"end":140539769,"strand":1,"feature_type":"variation","start":140539756,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140539757,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140539757,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs533515439","clinical_significance":[]},{"seq_region_name":"7","id":"rs891839339","clinical_significance":[],"strand":1,"feature_type":"variation","end":140539758,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539758,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140539759,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539759,"source":"dbSNP","seq_region_name":"7","id":"rs528186038","clinical_significance":[]},{"id":"rs911206283","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140539766,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539766,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140539771,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539771,"source":"dbSNP","seq_region_name":"7","id":"rs1563125801","clinical_significance":[]},{"start":140539781,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140539781,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1252423961","clinical_significance":[]},{"id":"rs964118263","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539782,"source":"dbSNP","strand":1,"feature_type":"variation","end":140539782,"alleles":["G","A"]},{"feature_type":"variation","strand":1,"end":140539782,"alleles":["G","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539782,"clinical_significance":[],"seq_region_name":"7","id":"rs1351499333"},{"end":140539783,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140539783,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1563125807","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1237506445","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140539784,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539784,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1796590489","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140539786,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539786,"source":"dbSNP"},{"seq_region_name":"7","id":"rs2130506579","clinical_significance":[],"start":140539788,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140539788,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1585580933","clinical_significance":[],"start":140539790,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140539790,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs990189748","clinical_significance":[],"start":140539791,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140539791,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539794,"feature_type":"variation","strand":1,"end":140539794,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1796590918"},{"feature_type":"variation","strand":1,"end":140539796,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539796,"clinical_significance":[],"seq_region_name":"7","id":"rs1014382254"},{"id":"rs73487622","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539799,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140539799},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796591232","feature_type":"variation","strand":1,"end":140539801,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539801},{"feature_type":"variation","strand":1,"end":140539805,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539805,"clinical_significance":[],"id":"rs773797930","seq_region_name":"7"},{"seq_region_name":"7","id":"rs946210675","clinical_significance":[],"strand":1,"feature_type":"variation","end":140539808,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539808,"source":"dbSNP"},{"seq_region_name":"7","id":"rs191487350","clinical_significance":[],"start":140539811,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140539811,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1041869346","feature_type":"variation","strand":1,"end":140539816,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539816},{"end":140539817,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140539817,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1563125838"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796592198","source":"dbSNP","start":140539821,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140539821,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140539823,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TTCTT","TT"],"end":140539827,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796592338"},{"id":"rs74942626","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539830,"source":"dbSNP","strand":1,"feature_type":"variation","end":140539830,"alleles":["C","T"]},{"end":140539831,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140539831,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs77448387","clinical_significance":[]},{"id":"rs1016628831","seq_region_name":"7","clinical_significance":[],"end":140539832,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140539832,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140539833,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140539833,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585581028"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539835,"source":"dbSNP","strand":1,"feature_type":"variation","end":140539835,"alleles":["A","G"],"id":"rs1796592998","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","C"],"end":140539836,"feature_type":"variation","strand":1,"source":"dbSNP","start":140539836,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs535981421"},{"source":"dbSNP","start":140539838,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140539838,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1423050684"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539840,"feature_type":"variation","strand":1,"end":140539840,"alleles":["C","T"],"clinical_significance":[],"id":"rs1170987498","seq_region_name":"7"},{"end":140539841,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140539841,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs10952731","clinical_significance":[]},{"clinical_significance":[],"id":"rs1193974028","seq_region_name":"7","source":"dbSNP","start":140539842,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140539842,"alleles":["T","C"],"feature_type":"variation","strand":1},{"id":"rs566157343","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140539843,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539843,"source":"dbSNP"},{"source":"dbSNP","start":140539845,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140539845,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1796594113","seq_region_name":"7"},{"start":140539850,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140539850,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796594267","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1460460039","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539850,"feature_type":"variation","strand":1,"end":140539851,"alleles":["GG","G"]},{"clinical_significance":[],"id":"rs1251298618","seq_region_name":"7","alleles":["G","A","T"],"end":140539855,"feature_type":"variation","strand":1,"source":"dbSNP","start":140539855,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796594798","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539856,"feature_type":"variation","strand":1,"end":140539856,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796594921","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539857,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140539857},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539858,"feature_type":"variation","strand":1,"end":140539858,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs894811852"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140539865,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539865,"clinical_significance":[],"id":"rs1796595091","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140539866,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539866,"source":"dbSNP","seq_region_name":"7","id":"rs1306856046","clinical_significance":[]},{"end":140539869,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","start":140539869,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1447859833","clinical_significance":[]},{"id":"rs972388542","seq_region_name":"7","clinical_significance":[],"end":140539871,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140539871,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1286407431","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140539872,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539872},{"clinical_significance":[],"seq_region_name":"7","id":"rs1203512934","feature_type":"variation","strand":1,"end":140539873,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539873},{"alleles":["T","C"],"end":140539874,"feature_type":"variation","strand":1,"source":"dbSNP","start":140539874,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796595742"},{"source":"dbSNP","start":140539875,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140539875,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs533518604"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539876,"source":"dbSNP","strand":1,"feature_type":"variation","end":140539876,"alleles":["G","A"],"seq_region_name":"7","id":"rs1796596043","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140539879,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539879,"source":"dbSNP","seq_region_name":"7","id":"rs1585581161","clinical_significance":[]},{"id":"rs1796596321","seq_region_name":"7","clinical_significance":[],"end":140539882,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140539882,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1563125906","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140539883,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539883},{"source":"dbSNP","start":140539888,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140539888,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130506916"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539889,"feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140539889,"clinical_significance":[],"seq_region_name":"7","id":"rs757275293"},{"clinical_significance":[],"seq_region_name":"7","id":"rs955101132","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539897,"feature_type":"variation","strand":1,"end":140539897,"alleles":["C","A","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1310723738","alleles":["G","A"],"end":140539898,"feature_type":"variation","strand":1,"source":"dbSNP","start":140539898,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539898,"source":"dbSNP","strand":1,"feature_type":"variation","end":140539901,"alleles":["GGGG","GGG"],"seq_region_name":"7","id":"rs1416204940","clinical_significance":[]},{"id":"rs1796597313","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140539900,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539900,"source":"dbSNP"},{"end":140539901,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140539901,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs558830179","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539903,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140539903,"seq_region_name":"7","id":"rs553872596","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796597737","alleles":["A","G"],"end":140539904,"feature_type":"variation","strand":1,"source":"dbSNP","start":140539904,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796597864","alleles":["A","C","G"],"end":140539907,"feature_type":"variation","strand":1,"source":"dbSNP","start":140539907,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140539908,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140539908,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1435279317","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796598156","clinical_significance":[],"strand":1,"feature_type":"variation","end":140539922,"alleles":["TGTGGAGCCATTTGT","TGT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539908,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140539910,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539910,"source":"dbSNP","seq_region_name":"7","id":"rs986672699","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796598435","clinical_significance":[],"strand":1,"feature_type":"variation","end":140539910,"alleles":["T","TT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539910,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1228116913","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140539913,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539913,"source":"dbSNP"},{"id":"rs182517321","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539918,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140539918},{"alleles":["T","G"],"end":140539919,"strand":1,"feature_type":"variation","start":140539919,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs911041817","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539921,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140539921,"seq_region_name":"7","id":"rs1796599022","clinical_significance":[]},{"clinical_significance":[],"id":"rs1796599146","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539924,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140539924},{"clinical_significance":[],"seq_region_name":"7","id":"rs544399388","feature_type":"variation","strand":1,"end":140539934,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539934},{"clinical_significance":[],"id":"rs377393838","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539935,"feature_type":"variation","strand":1,"end":140539935,"alleles":["G","A","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796599562","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140539942,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539942},{"clinical_significance":[],"id":"rs1422786472","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140539956,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539956},{"clinical_significance":[],"seq_region_name":"7","id":"rs1190458197","feature_type":"variation","strand":1,"end":140539957,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539957},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563125963","source":"dbSNP","start":140539961,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140539961,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs574677430","clinical_significance":[],"strand":1,"feature_type":"variation","end":140539962,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539962,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539964,"source":"dbSNP","strand":1,"feature_type":"variation","end":140539964,"alleles":["C","T"],"seq_region_name":"7","id":"rs754257822","clinical_significance":[]},{"seq_region_name":"7","id":"rs1244090590","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539965,"source":"dbSNP","strand":1,"feature_type":"variation","end":140539965,"alleles":["G","A","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539967,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140539967,"seq_region_name":"7","id":"rs1214485662","clinical_significance":[]},{"end":140539967,"alleles":["A","AA"],"strand":1,"feature_type":"variation","start":140539967,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1563125974","clinical_significance":[]},{"end":140539970,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140539970,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796600437","clinical_significance":[]},{"seq_region_name":"7","id":"rs955499758","clinical_significance":[],"end":140539971,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140539971,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1226905850","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539972,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140539972},{"seq_region_name":"7","id":"rs1008078721","clinical_significance":[],"strand":1,"feature_type":"variation","end":140539973,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539973,"source":"dbSNP"},{"alleles":["G","A"],"end":140539974,"strand":1,"feature_type":"variation","start":140539974,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs925203258","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796600930","alleles":["G","A"],"end":140539978,"feature_type":"variation","strand":1,"source":"dbSNP","start":140539978,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796601023","alleles":["C","G"],"end":140539986,"feature_type":"variation","strand":1,"source":"dbSNP","start":140539986,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796601104","alleles":["CATGCGG","CATGCGGAGGAGGACTTGACGCCTCCGCCTTTTTGCATGCGG"],"end":140539992,"feature_type":"variation","strand":1,"source":"dbSNP","start":140539986,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs542378969","alleles":["T","C","G"],"end":140539988,"feature_type":"variation","strand":1,"source":"dbSNP","start":140539988,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140539990,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140539990,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1053013324","clinical_significance":[]},{"seq_region_name":"7","id":"rs1362157578","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539991,"source":"dbSNP","strand":1,"feature_type":"variation","end":140539991,"alleles":["G","A"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140539994,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140539994,"clinical_significance":[],"id":"rs891914383","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1796601537","clinical_significance":[],"end":140539996,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140539996,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140539997,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140539997,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796601634","clinical_significance":[]},{"seq_region_name":"7","id":"rs1397516087","clinical_significance":[],"strand":1,"feature_type":"variation","end":140539998,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140539998,"source":"dbSNP"},{"alleles":["G","A"],"end":140539999,"strand":1,"feature_type":"variation","start":140539999,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1486057172","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1313017373","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140540000,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540000},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130507275","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540002,"feature_type":"variation","strand":1,"end":140540002,"alleles":["T","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs950134654","feature_type":"variation","strand":1,"end":140540005,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540005},{"clinical_significance":[],"seq_region_name":"7","id":"rs990071788","feature_type":"variation","strand":1,"end":140540006,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540006},{"start":140540009,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140540009,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs10808050","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140540010,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540010,"clinical_significance":[],"id":"rs967462822","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540011,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140540011,"clinical_significance":[],"id":"rs2130507323","seq_region_name":"7"},{"end":140540013,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140540013,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs765569190","clinical_significance":[]},{"seq_region_name":"7","id":"rs906012785","clinical_significance":[],"alleles":["C","T"],"end":140540017,"strand":1,"feature_type":"variation","start":140540017,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1191786251","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540017,"source":"dbSNP","strand":1,"feature_type":"variation","end":140540019,"alleles":["CCC","CC"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540018,"source":"dbSNP","strand":1,"feature_type":"variation","end":140540018,"alleles":["C","T"],"id":"rs1796602775","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140540019,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540019,"clinical_significance":[],"seq_region_name":"7","id":"rs1796602859"},{"source":"dbSNP","start":140540020,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C","G"],"end":140540020,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1001681681"},{"strand":1,"feature_type":"variation","end":140540026,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540026,"source":"dbSNP","seq_region_name":"7","id":"rs1796603058","clinical_significance":[]},{"id":"rs1796603160","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540027,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140540027},{"seq_region_name":"7","id":"rs1017606822","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140540028,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540028,"source":"dbSNP"},{"seq_region_name":"7","id":"rs898714411","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140540029,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540029,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540038,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140540038,"clinical_significance":[],"seq_region_name":"7","id":"rs1796603595"},{"start":140540039,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140540039,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","id":"rs1167923125","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796603821","clinical_significance":[],"strand":1,"feature_type":"variation","end":140540040,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540040,"source":"dbSNP"},{"end":140540043,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140540043,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796603914"},{"feature_type":"variation","strand":1,"end":140540045,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540045,"clinical_significance":[],"seq_region_name":"7","id":"rs1796604007"},{"clinical_significance":[],"id":"rs1563126065","seq_region_name":"7","feature_type":"variation","strand":1,"end":140540046,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540046},{"clinical_significance":[],"seq_region_name":"7","id":"rs1237431759","source":"dbSNP","start":140540047,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140540047,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585581622","source":"dbSNP","start":140540048,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140540048,"alleles":["T","G"],"feature_type":"variation","strand":1},{"start":140540049,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140540049,"alleles":["C","A","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs187178249","clinical_significance":[]},{"seq_region_name":"7","id":"rs1395115463","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["CCCCCC","CCCCC"],"end":140540054,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540049,"source":"dbSNP"},{"id":"rs1025313834","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140540052,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540052,"source":"dbSNP"},{"alleles":["C","G"],"end":140540054,"strand":1,"feature_type":"variation","start":140540054,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796604668","clinical_significance":[]},{"clinical_significance":[],"id":"rs1796604774","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140540057,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540057},{"id":"rs1796604867","seq_region_name":"7","clinical_significance":[],"start":140540058,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140540058,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540062,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140540062,"clinical_significance":[],"id":"rs1796604961","seq_region_name":"7"},{"id":"rs567582531","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140540064,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540064,"source":"dbSNP"},{"start":140540065,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140540065,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs955133634","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796605248","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540071,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140540071},{"seq_region_name":"7","id":"rs1796605328","clinical_significance":[],"end":140540074,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140540074,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140540075,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140540075,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1201825568","clinical_significance":[]},{"end":140540075,"alleles":["A","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140540075,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796605502"},{"start":140540077,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140540077,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs200249212","clinical_significance":[]},{"end":140540078,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140540078,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796605717","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140540083,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540083,"clinical_significance":[],"seq_region_name":"7","id":"rs1358216802"},{"seq_region_name":"7","id":"rs777045086","clinical_significance":[],"start":140540084,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140540084,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140540086,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140540086,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796606021"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563126098","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140540091,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540091},{"seq_region_name":"7","id":"rs1302209344","clinical_significance":[],"start":140540092,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140540092,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1796606249","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540094,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140540094},{"clinical_significance":[],"id":"rs1431086549","seq_region_name":"7","source":"dbSNP","start":140540098,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140540098,"alleles":["C","T"],"feature_type":"variation","strand":1},{"id":"rs1796606439","seq_region_name":"7","clinical_significance":[],"start":140540101,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140540101,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540104,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140540104,"seq_region_name":"7","id":"rs1018010769","clinical_significance":[]},{"source":"dbSNP","start":140540114,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140540114,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130507669"},{"clinical_significance":[],"seq_region_name":"7","id":"rs564802018","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540115,"feature_type":"variation","strand":1,"end":140540115,"alleles":["G","C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796606756","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540117,"feature_type":"variation","strand":1,"end":140540117,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs964241806","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140540118,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540118},{"clinical_significance":[],"id":"rs1796606920","seq_region_name":"7","source":"dbSNP","start":140540125,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140540125,"alleles":["C","T"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540126,"source":"dbSNP","strand":1,"feature_type":"variation","end":140540126,"alleles":["C","G","T"],"seq_region_name":"7","id":"rs1038017830","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540129,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140540129,"clinical_significance":[],"seq_region_name":"7","id":"rs1433478224"},{"clinical_significance":[],"seq_region_name":"7","id":"rs979247063","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540133,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140540133},{"clinical_significance":[],"seq_region_name":"7","id":"rs925197372","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540134,"feature_type":"variation","strand":1,"end":140540134,"alleles":["G","A","C","T"]},{"alleles":["TTT","TT"],"end":140540140,"feature_type":"variation","strand":1,"source":"dbSNP","start":140540138,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1796607617","seq_region_name":"7"},{"id":"rs1796607766","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540141,"source":"dbSNP","strand":1,"feature_type":"variation","end":140540141,"alleles":["C","G"]},{"seq_region_name":"7","id":"rs935253656","clinical_significance":[],"end":140540145,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140540145,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130507778","end":140540146,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140540146,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs988810557","clinical_significance":[],"alleles":["C","T"],"end":140540149,"strand":1,"feature_type":"variation","start":140540149,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["G","A","C","T"],"end":140540150,"feature_type":"variation","strand":1,"source":"dbSNP","start":140540150,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1236705637"},{"alleles":["C","T"],"end":140540153,"strand":1,"feature_type":"variation","start":140540153,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1198459245","clinical_significance":[]},{"start":140540154,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140540154,"strand":1,"feature_type":"variation","id":"rs1457010308","seq_region_name":"7","clinical_significance":[]},{"end":140540157,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140540157,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796608834"},{"seq_region_name":"7","id":"rs1585581857","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540161,"source":"dbSNP","strand":1,"feature_type":"variation","end":140540161,"alleles":["C","T"]},{"id":"rs1796609094","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540168,"source":"dbSNP","strand":1,"feature_type":"variation","end":140540168,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs531959471","clinical_significance":[],"start":140540169,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A","C"],"end":140540169,"strand":1,"feature_type":"variation"},{"end":140540172,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140540172,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs12670146","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs781254759","source":"dbSNP","start":140540174,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140540174,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1045806800","end":140540178,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140540178,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140540181,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540181,"clinical_significance":[],"seq_region_name":"7","id":"rs374472694"},{"seq_region_name":"7","id":"rs1311811291","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540182,"source":"dbSNP","strand":1,"feature_type":"variation","end":140540182,"alleles":["G","A"]},{"id":"rs1328991101","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140540183,"strand":1,"feature_type":"variation","start":140540183,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540192,"source":"dbSNP","strand":1,"feature_type":"variation","end":140540192,"alleles":["G","A"],"seq_region_name":"7","id":"rs1796610368","clinical_significance":[]},{"start":140540196,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140540196,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796610522","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540197,"feature_type":"variation","strand":1,"end":140540197,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1796610656"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796610796","feature_type":"variation","strand":1,"end":140540198,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540198},{"start":140540203,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140540203,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1445800500","clinical_significance":[]},{"alleles":["T","C","G"],"end":140540206,"strand":1,"feature_type":"variation","start":140540206,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs905923234","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540206,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TCC","TCCTCC"],"end":140540208,"seq_region_name":"7","id":"rs1796611190","clinical_significance":[]},{"id":"rs568349038","seq_region_name":"7","clinical_significance":[],"alleles":["C","A"],"end":140540207,"strand":1,"feature_type":"variation","start":140540207,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs546237939","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540210,"source":"dbSNP","strand":1,"feature_type":"variation","end":140540210,"alleles":["C","T"]},{"clinical_significance":[],"id":"rs561828679","seq_region_name":"7","end":140540215,"alleles":["CGTTCC","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140540210,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs898782762","end":140540211,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140540211,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1159987210","alleles":["TTCCTGCT","T"],"end":140540219,"feature_type":"variation","strand":1,"source":"dbSNP","start":140540212,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs115296074","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140540214,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540214},{"source":"dbSNP","start":140540218,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","-"],"end":140540218,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs530488297"},{"clinical_significance":[],"id":"rs770208410","seq_region_name":"7","source":"dbSNP","start":140540222,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140540222,"alleles":["C","T"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140540230,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540230,"source":"dbSNP","seq_region_name":"7","id":"rs1178361774","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs963906470","source":"dbSNP","start":140540230,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["CTCC","C"],"end":140540233,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140540232,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140540232,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796612198"},{"end":140540240,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140540240,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1011548877","clinical_significance":[]},{"clinical_significance":[],"id":"rs1796612354","seq_region_name":"7","alleles":["T","C"],"end":140540247,"feature_type":"variation","strand":1,"source":"dbSNP","start":140540247,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140540248,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540248,"clinical_significance":[],"seq_region_name":"7","id":"rs1188938857"},{"seq_region_name":"7","id":"rs1796612517","clinical_significance":[],"strand":1,"feature_type":"variation","end":140540253,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540253,"source":"dbSNP"},{"source":"dbSNP","start":140540256,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140540256,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1021615572"},{"seq_region_name":"7","id":"rs147668337","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540257,"source":"dbSNP","strand":1,"feature_type":"variation","end":140540257,"alleles":["G","A"]},{"alleles":["A","C"],"end":140540264,"feature_type":"variation","strand":1,"source":"dbSNP","start":140540264,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs566196374"},{"source":"dbSNP","start":140540266,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140540266,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1264330599"},{"source":"dbSNP","start":140540268,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140540268,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1347267544"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796612984","alleles":["C","T"],"end":140540270,"feature_type":"variation","strand":1,"source":"dbSNP","start":140540270,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140540273,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540273,"source":"dbSNP","seq_region_name":"7","id":"rs1796613084","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140540278,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540278,"source":"dbSNP","seq_region_name":"7","id":"rs1036303519","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs960244468","alleles":["A","G"],"end":140540280,"feature_type":"variation","strand":1,"source":"dbSNP","start":140540280,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140540281,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540281,"clinical_significance":[],"seq_region_name":"7","id":"rs192135304"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796613593","end":140540284,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140540284,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585582131","end":140540288,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140540288,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs74738161","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540289,"feature_type":"variation","strand":1,"end":140540289,"alleles":["C","T"]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140540294,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540294,"source":"dbSNP","id":"rs963792748","seq_region_name":"7","clinical_significance":[]},{"start":140540296,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140540296,"strand":1,"feature_type":"variation","id":"rs1001138840","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs184684371","feature_type":"variation","strand":1,"end":140540298,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540298},{"clinical_significance":[],"seq_region_name":"7","id":"rs537793820","alleles":["G","A"],"end":140540299,"feature_type":"variation","strand":1,"source":"dbSNP","start":140540299,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1273129570","feature_type":"variation","strand":1,"end":140540305,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540305},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540306,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140540306,"seq_region_name":"7","id":"rs1385285534","clinical_significance":[]},{"seq_region_name":"7","id":"rs1390338568","clinical_significance":[],"start":140540310,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140540310,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs973762834","alleles":["C","T"],"end":140540311,"feature_type":"variation","strand":1,"source":"dbSNP","start":140540311,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1224499538","seq_region_name":"7","clinical_significance":[],"alleles":["G","A","T"],"end":140540312,"strand":1,"feature_type":"variation","start":140540312,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["GGAG","G"],"end":140540319,"strand":1,"feature_type":"variation","start":140540316,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs550772187","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585582233","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540320,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140540320},{"id":"rs1158581762","seq_region_name":"7","clinical_significance":[],"start":140540322,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140540322,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1796614924","seq_region_name":"7","source":"dbSNP","start":140540324,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140540324,"alleles":["G","A"],"feature_type":"variation","strand":1},{"alleles":["T","G"],"end":140540329,"strand":1,"feature_type":"variation","start":140540329,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585582260","clinical_significance":[]},{"seq_region_name":"7","id":"rs919581431","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540330,"source":"dbSNP","strand":1,"feature_type":"variation","end":140540330,"alleles":["G","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585582281","end":140540335,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140540335,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1585582298","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140540337,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540337,"source":"dbSNP"},{"id":"rs956644255","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140540338,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540338,"source":"dbSNP"},{"id":"rs1326739414","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140540339,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540339,"source":"dbSNP"},{"alleles":["G","A"],"end":140540340,"strand":1,"feature_type":"variation","start":140540340,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1207876908","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540344,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140540344,"seq_region_name":"7","id":"rs1197264639","clinical_significance":[]},{"start":140540346,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G","T"],"end":140540346,"strand":1,"feature_type":"variation","id":"rs73487630","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540347,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140540347,"clinical_significance":[],"id":"rs1266253421","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140540348,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540348,"clinical_significance":[],"seq_region_name":"7","id":"rs1796615771"},{"source":"dbSNP","start":140540350,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140540350,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1186531674"},{"clinical_significance":[],"id":"rs917803499","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140540352,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540352},{"end":140540354,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140540354,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130508367"},{"feature_type":"variation","strand":1,"end":140540355,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540355,"clinical_significance":[],"seq_region_name":"7","id":"rs1283342684"},{"start":140540360,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140540360,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796616100","clinical_significance":[]},{"clinical_significance":[],"id":"rs140774922","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540361,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140540361},{"seq_region_name":"7","id":"rs1348565115","clinical_significance":[],"start":140540365,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140540365,"alleles":["T","G"],"strand":1,"feature_type":"variation"},{"id":"rs368218755","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140540370,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540370,"source":"dbSNP"},{"start":140540371,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140540371,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs981373986","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140540377,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540377,"clinical_significance":[],"seq_region_name":"7","id":"rs2130508435"},{"clinical_significance":[],"seq_region_name":"7","id":"rs775909354","end":140540380,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140540380,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140540382,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540382,"source":"dbSNP","seq_region_name":"7","id":"rs73487632","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs770506742","end":140540383,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140540383,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140540390,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140540390,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1338517382"},{"alleles":["G","A"],"end":140540395,"feature_type":"variation","strand":1,"source":"dbSNP","start":140540395,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796617041"},{"seq_region_name":"7","id":"rs1796617111","clinical_significance":[],"alleles":["C","T"],"end":140540397,"strand":1,"feature_type":"variation","start":140540397,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140540403,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140540403,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1472097813"},{"source":"dbSNP","start":140540407,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140540407,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1038968659"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1011432720","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140540410,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540410},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540412,"source":"dbSNP","strand":1,"feature_type":"variation","end":140540412,"alleles":["T","A"],"seq_region_name":"7","id":"rs1158871599","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540414,"source":"dbSNP","strand":1,"feature_type":"variation","end":140540414,"alleles":["T","C"],"seq_region_name":"7","id":"rs1377844029","clinical_significance":[]},{"clinical_significance":[],"id":"rs774059432","seq_region_name":"7","end":140540415,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140540415,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796617741","feature_type":"variation","strand":1,"end":140540417,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540417},{"source":"dbSNP","start":140540419,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140540419,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1022084363"},{"start":140540421,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140540421,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs554314067","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140540428,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540428,"source":"dbSNP","id":"rs1170701669","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1478631171","source":"dbSNP","start":140540445,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140540445,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540448,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140540448,"id":"rs1260377094","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540455,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140540455,"clinical_significance":[],"seq_region_name":"7","id":"rs1796618270"},{"source":"dbSNP","start":140540467,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140540467,"alleles":["G","C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1796618360","seq_region_name":"7"},{"start":140540468,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140540468,"strand":1,"feature_type":"variation","id":"rs4576348","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140540474,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540474,"clinical_significance":[],"id":"rs1485934528","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540476,"feature_type":"variation","strand":1,"end":140540476,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs879287889"},{"seq_region_name":"7","id":"rs1796618756","clinical_significance":[],"end":140540482,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140540482,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1047365232","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540484,"source":"dbSNP","strand":1,"feature_type":"variation","end":140540484,"alleles":["G","C"]},{"feature_type":"variation","strand":1,"end":140540487,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540487,"clinical_significance":[],"seq_region_name":"7","id":"rs1796618912"},{"alleles":["G","A"],"end":140540495,"strand":1,"feature_type":"variation","start":140540495,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796618990","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540501,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140540501,"id":"rs1198457188","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs891346837","clinical_significance":[],"end":140540502,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140540502,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585582620","source":"dbSNP","start":140540507,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140540507,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796619311","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140540510,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540510},{"feature_type":"variation","strand":1,"end":140540512,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540512,"clinical_significance":[],"seq_region_name":"7","id":"rs1796619390"},{"clinical_significance":[],"id":"rs1344041445","seq_region_name":"7","source":"dbSNP","start":140540515,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140540515,"alleles":["G","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1796619482","clinical_significance":[],"end":140540518,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140540518,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1443031753","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540519,"feature_type":"variation","strand":1,"end":140540519,"alleles":["A","-"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796619660","feature_type":"variation","strand":1,"end":140540521,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540521},{"start":140540523,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140540523,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs999229124","clinical_significance":[]},{"seq_region_name":"7","id":"rs1316350509","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540525,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140540525},{"id":"rs1796620003","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540528,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["-","TGTT"],"end":140540527},{"seq_region_name":"7","id":"rs1277615626","clinical_significance":[],"alleles":["C","T"],"end":140540529,"strand":1,"feature_type":"variation","start":140540529,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540536,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140540536,"id":"rs546273125","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1007902893","source":"dbSNP","start":140540537,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140540537,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796620369","feature_type":"variation","strand":1,"end":140540539,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540539},{"id":"rs1585582707","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540549,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140540549},{"seq_region_name":"7","id":"rs564363778","clinical_significance":[],"alleles":["C","T"],"end":140540550,"strand":1,"feature_type":"variation","start":140540550,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796620628","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140540552,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540552},{"source":"dbSNP","start":140540554,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140540554,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1342720755"},{"seq_region_name":"7","id":"rs4236489","clinical_significance":[],"start":140540555,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140540555,"alleles":["G","A","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1796620805","seq_region_name":"7","source":"dbSNP","start":140540565,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140540565,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540567,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140540567,"clinical_significance":[],"seq_region_name":"7","id":"rs1563126378"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540568,"feature_type":"variation","strand":1,"end":140540568,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs372342058"},{"source":"dbSNP","start":140540579,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140540579,"alleles":["G","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1397639830","seq_region_name":"7"},{"start":140540582,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140540582,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1333846003","clinical_significance":[]},{"clinical_significance":[],"id":"rs1796621133","seq_region_name":"7","source":"dbSNP","start":140540585,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140540585,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540589,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140540589,"clinical_significance":[],"seq_region_name":"7","id":"rs1796621231"},{"source":"dbSNP","start":140540591,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140540591,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1466834731"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140540594,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540594,"clinical_significance":[],"seq_region_name":"7","id":"rs1421060493"},{"alleles":["G","A","C"],"end":140540596,"strand":1,"feature_type":"variation","start":140540596,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1032617615","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140540602,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540602,"clinical_significance":[],"id":"rs956551536","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1796621711","clinical_significance":[],"start":140540603,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140540603,"strand":1,"feature_type":"variation"},{"id":"rs1796621858","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540610,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140540610},{"clinical_significance":[],"seq_region_name":"7","id":"rs1009331548","source":"dbSNP","start":140540612,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140540612,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs149810818","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540613,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140540613},{"seq_region_name":"7","id":"rs1024850318","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540617,"source":"dbSNP","strand":1,"feature_type":"variation","end":140540617,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1585582853","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540618,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140540618},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540620,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140540620,"clinical_significance":[],"seq_region_name":"7","id":"rs1563126399"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585582863","alleles":["A","C"],"end":140540621,"feature_type":"variation","strand":1,"source":"dbSNP","start":140540621,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540622,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140540622,"seq_region_name":"7","id":"rs1200353764","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140540623,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540623,"clinical_significance":[],"seq_region_name":"7","id":"rs4289726"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1257676023","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540624,"feature_type":"variation","strand":1,"end":140540624,"alleles":["G","A","C"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540630,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140540630,"seq_region_name":"7","id":"rs529462097","clinical_significance":[]},{"seq_region_name":"7","id":"rs1282554688","clinical_significance":[],"strand":1,"feature_type":"variation","end":140540632,"alleles":["T","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540632,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540634,"feature_type":"variation","strand":1,"alleles":["T","A","G"],"end":140540634,"clinical_significance":[],"seq_region_name":"7","id":"rs1244670219"},{"seq_region_name":"7","id":"rs927298879","clinical_significance":[],"start":140540639,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140540639,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140540640,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140540640,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs959073778"},{"seq_region_name":"7","id":"rs4260823","clinical_significance":[],"alleles":["G","A"],"end":140540641,"strand":1,"feature_type":"variation","start":140540641,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140540642,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140540642,"alleles":["G","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585582952","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796624349","clinical_significance":[],"end":140540643,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140540643,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796624436","end":140540645,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140540645,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540648,"feature_type":"variation","strand":1,"end":140540648,"alleles":["T","C"],"clinical_significance":[],"id":"rs2130509010","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1397605275","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540661,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GG","G"],"end":140540662},{"end":140540663,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140540663,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs190580205","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140540664,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540664,"clinical_significance":[],"seq_region_name":"7","id":"rs527442769"},{"start":140540668,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140540668,"strand":1,"feature_type":"variation","id":"rs1796624829","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs930133743","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540669,"source":"dbSNP","strand":1,"feature_type":"variation","end":140540669,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs57565761","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140540670,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540670},{"source":"dbSNP","start":140540677,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140540677,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796625101"},{"source":"dbSNP","start":140540680,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140540680,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1472410092"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540683,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140540683,"clinical_significance":[],"seq_region_name":"7","id":"rs1796625272"},{"strand":1,"feature_type":"variation","end":140540687,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540687,"source":"dbSNP","seq_region_name":"7","id":"rs1796625360","clinical_significance":[]},{"seq_region_name":"7","id":"rs570390691","clinical_significance":[],"strand":1,"feature_type":"variation","end":140540688,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540688,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1796625551","clinical_significance":[],"strand":1,"feature_type":"variation","end":140540689,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540689,"source":"dbSNP"},{"start":140540691,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140540691,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs568759504","clinical_significance":[]},{"alleles":["C","A","T"],"end":140540693,"feature_type":"variation","strand":1,"source":"dbSNP","start":140540693,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs4262257"},{"seq_region_name":"7","id":"rs539562374","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140540695,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540695,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1042988314","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540696,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140540696},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540699,"source":"dbSNP","strand":1,"feature_type":"variation","end":140540699,"alleles":["C","G"],"id":"rs1411077451","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140540702,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540702,"clinical_significance":[],"seq_region_name":"7","id":"rs1309913948"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540705,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140540705,"seq_region_name":"7","id":"rs1796626248","clinical_significance":[]},{"source":"dbSNP","start":140540708,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140540708,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1287772927"},{"alleles":["C","A"],"end":140540709,"feature_type":"variation","strand":1,"source":"dbSNP","start":140540709,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130509179"},{"start":140540711,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140540711,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs903061017","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs368781332","source":"dbSNP","start":140540712,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140540712,"alleles":["G","T"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140540727,"alleles":["TTTCTTTCTTTCTTT","TTTCTTTCTTT","TTTCTTTCTTTCTTTCTTT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540713,"clinical_significance":[],"seq_region_name":"7","id":"rs753886983"},{"seq_region_name":"7","id":"rs1238346613","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["TTT","TTTTT"],"end":140540719,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540717,"source":"dbSNP"},{"alleles":["T","C"],"end":140540718,"strand":1,"feature_type":"variation","start":140540718,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130509237","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140540719,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540719,"source":"dbSNP","seq_region_name":"7","id":"rs998884720","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1036070324","source":"dbSNP","start":140540720,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140540720,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796627070","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540721,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140540721},{"alleles":["-","G"],"end":140540724,"feature_type":"variation","strand":1,"source":"dbSNP","start":140540725,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs796359327"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796627254","source":"dbSNP","start":140540725,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140540725,"alleles":["T","A"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540725,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TTTTTTTTTTTT","TTTTTTTT","TTTTTTTTTT","TTTTTTTTTTT","TTTTTTTTTTTTT","TTTTTTTTTTTTTT"],"end":140540736,"seq_region_name":"7","id":"rs375517319","clinical_significance":[]},{"clinical_significance":[],"id":"rs1796627638","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540726,"feature_type":"variation","strand":1,"alleles":["-","C"],"end":140540725},{"seq_region_name":"7","id":"rs568319006","clinical_significance":[],"start":140540727,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140540727,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1379427595","clinical_significance":[],"alleles":["T","C"],"end":140540728,"strand":1,"feature_type":"variation","start":140540728,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1191596453","source":"dbSNP","start":140540729,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140540729,"alleles":["T","G"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540733,"source":"dbSNP","strand":1,"feature_type":"variation","end":140540732,"alleles":["-","G"],"seq_region_name":"7","id":"rs1796628000","clinical_significance":[]},{"source":"dbSNP","start":140540734,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140540734,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796628097"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540736,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140540736,"seq_region_name":"7","id":"rs1479105747","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140540737,"alleles":["A","AA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540737,"source":"dbSNP","seq_region_name":"7","id":"rs1245223349","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540738,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140540738,"id":"rs1796628387","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796628468","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540742,"source":"dbSNP","strand":1,"feature_type":"variation","end":140540742,"alleles":["G","T"]},{"clinical_significance":[],"id":"rs1198178998","seq_region_name":"7","feature_type":"variation","strand":1,"end":140540744,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540744},{"alleles":["C","T"],"end":140540748,"strand":1,"feature_type":"variation","start":140540748,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1012987542","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540749,"feature_type":"variation","strand":1,"end":140540749,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1288337096"},{"seq_region_name":"7","id":"rs1796628829","clinical_significance":[],"strand":1,"feature_type":"variation","end":140540754,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540754,"source":"dbSNP"},{"end":140540756,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140540756,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796628936"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140540757,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540757,"source":"dbSNP","seq_region_name":"7","id":"rs1215071551","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796629128","clinical_significance":[],"start":140540758,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140540758,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"end":140540760,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140540760,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130509443"},{"seq_region_name":"7","id":"rs1796629215","clinical_significance":[],"start":140540765,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140540765,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540769,"source":"dbSNP","strand":1,"feature_type":"variation","end":140540769,"alleles":["G","C","T"],"seq_region_name":"7","id":"rs1023176025","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585583255","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540770,"source":"dbSNP","strand":1,"feature_type":"variation","end":140540770,"alleles":["T","G"]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140540771,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540771,"clinical_significance":[],"seq_region_name":"7","id":"rs1796629577"},{"seq_region_name":"7","id":"rs936305264","clinical_significance":[],"strand":1,"feature_type":"variation","end":140540772,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540772,"source":"dbSNP"},{"start":140540773,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C"],"end":140540773,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1242345658","clinical_significance":[]},{"seq_region_name":"7","id":"rs1435391236","clinical_significance":[],"alleles":["A","G"],"end":140540779,"strand":1,"feature_type":"variation","start":140540779,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140540780,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140540780,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs1340577912","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1283447783","alleles":["A","G"],"end":140540782,"feature_type":"variation","strand":1,"source":"dbSNP","start":140540782,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1339977236","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140540786,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540786,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140540787,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540787,"clinical_significance":[],"seq_region_name":"7","id":"rs557529624"},{"strand":1,"feature_type":"variation","end":140540788,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540788,"source":"dbSNP","seq_region_name":"7","id":"rs1359854726","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796630591","alleles":["C","T"],"end":140540789,"feature_type":"variation","strand":1,"source":"dbSNP","start":140540789,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs892176581","seq_region_name":"7","source":"dbSNP","start":140540791,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140540791,"alleles":["C","A"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140540792,"alleles":["T","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540792,"source":"dbSNP","seq_region_name":"7","id":"rs10265467","clinical_significance":[]},{"seq_region_name":"7","id":"rs1423246940","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140540794,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540794,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140540805,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540805,"source":"dbSNP","seq_region_name":"7","id":"rs1340876583","clinical_significance":[]},{"alleles":["A","G"],"end":140540811,"feature_type":"variation","strand":1,"source":"dbSNP","start":140540811,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs750724515","seq_region_name":"7"},{"seq_region_name":"7","id":"rs554054534","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540812,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140540812},{"seq_region_name":"7","id":"rs1478305452","clinical_significance":[],"alleles":["G","C","T"],"end":140540813,"strand":1,"feature_type":"variation","start":140540813,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540815,"source":"dbSNP","strand":1,"feature_type":"variation","end":140540815,"alleles":["T","A"],"seq_region_name":"7","id":"rs1265402836","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1191652322","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140540825,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540825},{"source":"dbSNP","start":140540836,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140540836,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1796631628","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796631713","feature_type":"variation","strand":1,"end":140540840,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540840},{"seq_region_name":"7","id":"rs1488229046","clinical_significance":[],"end":140540842,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140540842,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1024761449","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140540843,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540843},{"source":"dbSNP","start":140540844,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140540844,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs982500075","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1310799196","clinical_significance":[],"start":140540845,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140540845,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"end":140540846,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140540846,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796632160","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs34848218","feature_type":"variation","strand":1,"alleles":["GGG","GGGG"],"end":140540853,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540851},{"end":140540852,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140540852,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796632325"},{"seq_region_name":"7","id":"rs1278425976","clinical_significance":[],"strand":1,"feature_type":"variation","end":140540861,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540861,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1211093625","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140540863,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540863,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796632725","source":"dbSNP","start":140540864,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140540864,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs572196570","end":140540866,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140540866,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140540867,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140540867,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1259193140","seq_region_name":"7"},{"id":"rs912213857","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540868,"source":"dbSNP","strand":1,"feature_type":"variation","end":140540868,"alleles":["C","G","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs374830075","end":140540871,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140540871,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1185856011","clinical_significance":[],"end":140540872,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140540872,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs773005061","feature_type":"variation","strand":1,"end":140540874,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540874},{"end":140540875,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140540875,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1476010068","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","A","G","T"],"end":140540878,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540878,"clinical_significance":[],"id":"rs975125464","seq_region_name":"7"},{"seq_region_name":"7","id":"rs920979028","clinical_significance":[],"start":140540880,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140540880,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1796633690","clinical_significance":[],"strand":1,"feature_type":"variation","end":140540885,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540885,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs539582604","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540891,"feature_type":"variation","strand":1,"end":140540891,"alleles":["T","C"]},{"end":140540893,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140540893,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1426090662"},{"alleles":["TTTTT","TTTT"],"end":140540897,"feature_type":"variation","strand":1,"source":"dbSNP","start":140540893,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796633947"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540897,"feature_type":"variation","strand":1,"end":140540897,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1796634053"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1002115059","end":140540902,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140540902,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140540904,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540904,"clinical_significance":[],"seq_region_name":"7","id":"rs947226330"},{"feature_type":"variation","strand":1,"end":140540906,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540906,"clinical_significance":[],"seq_region_name":"7","id":"rs1171069255"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140540907,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540907,"clinical_significance":[],"id":"rs1415080191","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796634384","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540907,"feature_type":"variation","strand":1,"end":140540909,"alleles":["GGG","GG"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563126646","end":140540909,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140540909,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1388351998","seq_region_name":"7","end":140540910,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140540910,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1043259351","seq_region_name":"7","source":"dbSNP","start":140540911,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140540911,"alleles":["T","A","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1237243815","end":140540919,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140540919,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","G"],"end":140540935,"strand":1,"feature_type":"variation","start":140540935,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796634873","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1199690023","feature_type":"variation","strand":1,"end":140540942,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540942},{"seq_region_name":"7","id":"rs1796635070","clinical_significance":[],"start":140540943,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140540943,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140540944,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540944,"source":"dbSNP","seq_region_name":"7","id":"rs1796635163","clinical_significance":[]},{"clinical_significance":[],"id":"rs1429202731","seq_region_name":"7","end":140540954,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140540954,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs2130509957","clinical_significance":[],"alleles":["A","G"],"end":140540961,"strand":1,"feature_type":"variation","start":140540961,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140540964,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540964,"source":"dbSNP","seq_region_name":"7","id":"rs6965765","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540965,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140540965,"clinical_significance":[],"seq_region_name":"7","id":"rs1796635517"},{"source":"dbSNP","start":140540967,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140540967,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1216190019"},{"clinical_significance":[],"seq_region_name":"7","id":"rs193130510","source":"dbSNP","start":140540969,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140540969,"alleles":["C","T"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540970,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140540970,"seq_region_name":"7","id":"rs185784844","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140540977,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540977,"source":"dbSNP","seq_region_name":"7","id":"rs1333235280","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140540978,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540978,"source":"dbSNP","seq_region_name":"7","id":"rs1027081380","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540981,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140540981,"clinical_significance":[],"id":"rs1376944297","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs951433132","source":"dbSNP","start":140540988,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140540988,"alleles":["G","A"],"feature_type":"variation","strand":1},{"end":140540989,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140540989,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796636166"},{"id":"rs1796636256","seq_region_name":"7","clinical_significance":[],"start":140540990,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140540990,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1057155942","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140540994,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540994,"source":"dbSNP"},{"start":140540997,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140540997,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs982985404","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140540998,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140540998,"source":"dbSNP","seq_region_name":"7","id":"rs527770426","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140540999,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140540999,"clinical_significance":[],"id":"rs2130510092","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541002,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140541002,"seq_region_name":"7","id":"rs1796636524","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs944316316","source":"dbSNP","start":140541003,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140541003,"alleles":["C","A","T"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140541005,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541005,"source":"dbSNP","seq_region_name":"7","id":"rs1796636729","clinical_significance":[]},{"end":140541008,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140541008,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1465365845","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796636945","alleles":["G","A"],"end":140541010,"feature_type":"variation","strand":1,"source":"dbSNP","start":140541010,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140541011,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140541011,"alleles":["C","A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs143771781"},{"seq_region_name":"7","id":"rs1796637160","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541015,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140541015},{"seq_region_name":"7","id":"rs1422532682","clinical_significance":[],"start":140541016,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140541016,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140541024,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140541024,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1413743973"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541025,"source":"dbSNP","strand":1,"feature_type":"variation","end":140541025,"alleles":["C","G"],"seq_region_name":"7","id":"rs1796637406","clinical_significance":[]},{"alleles":["G","A"],"end":140541029,"feature_type":"variation","strand":1,"source":"dbSNP","start":140541029,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs895816964"},{"seq_region_name":"7","id":"rs1585583841","clinical_significance":[],"start":140541030,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140541030,"alleles":["T","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796637664","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541033,"feature_type":"variation","strand":1,"end":140541033,"alleles":["C","G"]},{"source":"dbSNP","start":140541042,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140541042,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796637752"},{"start":140541044,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140541044,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796637831","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796637923","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140541053,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541053,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541057,"source":"dbSNP","strand":1,"feature_type":"variation","end":140541057,"alleles":["T","C"],"seq_region_name":"7","id":"rs1796638037","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1109939","feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140541062,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541062},{"alleles":["A","G"],"end":140541068,"feature_type":"variation","strand":1,"source":"dbSNP","start":140541068,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796638329"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140541074,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541074,"source":"dbSNP","seq_region_name":"7","id":"rs1044504999","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796638501","clinical_significance":[],"alleles":["A","G","T"],"end":140541080,"strand":1,"feature_type":"variation","start":140541080,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1796638580","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541083,"feature_type":"variation","strand":1,"end":140541083,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs936352150","feature_type":"variation","strand":1,"end":140541092,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541092},{"id":"rs1363749865","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541096,"source":"dbSNP","strand":1,"feature_type":"variation","end":140541096,"alleles":["G","C"]},{"feature_type":"variation","strand":1,"end":140541098,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541098,"clinical_significance":[],"id":"rs899207158","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140541099,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541099,"clinical_significance":[],"seq_region_name":"7","id":"rs1796638969"},{"clinical_significance":[],"seq_region_name":"7","id":"rs111609010","source":"dbSNP","start":140541102,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140541102,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541108,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140541108,"seq_region_name":"7","id":"rs1223155067","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140541111,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541111,"source":"dbSNP","seq_region_name":"7","id":"rs1053830495","clinical_significance":[]},{"alleles":["G","A","C"],"end":140541118,"strand":1,"feature_type":"variation","start":140541118,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796639361","clinical_significance":[]},{"start":140541118,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["GTTCCC","-"],"end":140541123,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1319811757","clinical_significance":[]},{"end":140541123,"alleles":["CCC","C"],"strand":1,"feature_type":"variation","start":140541121,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796639590","clinical_significance":[]},{"seq_region_name":"7","id":"rs1290950148","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541127,"source":"dbSNP","strand":1,"feature_type":"variation","end":140541127,"alleles":["T","G"]},{"end":140541130,"alleles":["TTTT","TTT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140541127,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796639747"},{"clinical_significance":[],"seq_region_name":"7","id":"rs892255392","source":"dbSNP","start":140541129,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140541129,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140541132,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140541132,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1378814397"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140541136,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541136,"clinical_significance":[],"seq_region_name":"7","id":"rs1234382934"},{"seq_region_name":"7","id":"rs1796640294","clinical_significance":[],"alleles":["T","C"],"end":140541138,"strand":1,"feature_type":"variation","start":140541138,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1796640438","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541140,"feature_type":"variation","strand":1,"end":140541140,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796640556","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541141,"feature_type":"variation","strand":1,"end":140541141,"alleles":["A","T"]},{"end":140541142,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140541142,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1446301966","clinical_significance":[]},{"seq_region_name":"7","id":"rs1563126754","clinical_significance":[],"alleles":["A","G"],"end":140541145,"strand":1,"feature_type":"variation","start":140541145,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140541145,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AA","AAA"],"end":140541146,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1281919520"},{"source":"dbSNP","start":140541148,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140541148,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs369836712"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1368604173","source":"dbSNP","start":140541149,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140541153,"alleles":["TTTTT","TTTT"],"feature_type":"variation","strand":1},{"alleles":["T","C"],"end":140541153,"feature_type":"variation","strand":1,"source":"dbSNP","start":140541153,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1295325780"},{"seq_region_name":"7","id":"rs1456461269","clinical_significance":[],"end":140541155,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140541155,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["TTTTTTTT","TTTTTTT","TTTTTTTTT"],"end":140541164,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541157,"clinical_significance":[],"seq_region_name":"7","id":"rs141354647"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796641866","source":"dbSNP","start":140541164,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140541164,"alleles":["T","C"],"feature_type":"variation","strand":1},{"id":"rs2130510525","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140541165,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541165,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796641965","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140541166,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541166},{"id":"rs2130510537","seq_region_name":"7","clinical_significance":[],"end":140541171,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140541171,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140541175,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140541175,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs777775683"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1422134101","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140541177,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541177},{"seq_region_name":"7","id":"rs1796642346","clinical_significance":[],"alleles":["A","T"],"end":140541181,"strand":1,"feature_type":"variation","start":140541181,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796642479","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541181,"feature_type":"variation","strand":1,"end":140541185,"alleles":["AGAGA","AGA"]},{"start":140541182,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140541182,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796642630","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140541183,"alleles":["A","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541183,"source":"dbSNP","seq_region_name":"7","id":"rs1378820459","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140541190,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541190,"source":"dbSNP","seq_region_name":"7","id":"rs1796642942","clinical_significance":[]},{"alleles":["G","GAGTCACTGGTG"],"end":140541190,"feature_type":"variation","strand":1,"source":"dbSNP","start":140541190,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796643081"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796643202","end":140541191,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140541191,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1199565641","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541191,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TCTCTCTCT","TCTCT","TCTCTCT"],"end":140541199},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541195,"feature_type":"variation","strand":1,"end":140541195,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1178462678"},{"clinical_significance":[],"seq_region_name":"7","id":"rs753628127","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541211,"feature_type":"variation","strand":1,"alleles":["G","A","C","T"],"end":140541211},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796643894","source":"dbSNP","start":140541214,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140541214,"alleles":["T","A","C"],"feature_type":"variation","strand":1},{"start":140541215,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C"],"end":140541215,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1192359902","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140541216,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541216,"clinical_significance":[],"seq_region_name":"7","id":"rs1278312634"},{"start":140541216,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["GTGTCTCACTGTACTTTTACC","-"],"end":140541236,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796644693","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796644847","alleles":["G","A"],"end":140541218,"feature_type":"variation","strand":1,"source":"dbSNP","start":140541218,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1447960400","clinical_significance":[],"start":140541220,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140541220,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs757105641","clinical_significance":[],"start":140541222,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140541222,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["C","A","G"],"end":140541229,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541229,"clinical_significance":[],"seq_region_name":"7","id":"rs1796645316"},{"seq_region_name":"7","id":"rs1109938","clinical_significance":[],"start":140541231,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140541231,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140541237,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140541237,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1246734072"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541245,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140541245,"seq_region_name":"7","id":"rs2130510735","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796645852","feature_type":"variation","strand":1,"end":140541249,"alleles":["G","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541249},{"end":140541252,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140541252,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs559563458","clinical_significance":[]},{"source":"dbSNP","start":140541253,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140541253,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1449459579"},{"start":140541258,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140541261,"alleles":["TTTT","TTT"],"strand":1,"feature_type":"variation","id":"rs201352277","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1194323536","clinical_significance":[],"start":140541263,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A","C","G"],"end":140541263,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1238102920","feature_type":"variation","strand":1,"end":140541265,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541265},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541265,"feature_type":"variation","strand":1,"end":140541269,"alleles":["CCCCC","CCCC"],"clinical_significance":[],"seq_region_name":"7","id":"rs1283560644"},{"strand":1,"feature_type":"variation","end":140541266,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541266,"source":"dbSNP","seq_region_name":"7","id":"rs1796646771","clinical_significance":[]},{"alleles":["C","A"],"end":140541267,"feature_type":"variation","strand":1,"source":"dbSNP","start":140541267,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1312925909"},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140541268,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541268,"source":"dbSNP","seq_region_name":"7","id":"rs1796647109","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796647257","source":"dbSNP","start":140541269,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140541269,"alleles":["C","T"],"feature_type":"variation","strand":1},{"end":140541288,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140541288,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1796647409","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796647528","clinical_significance":[],"alleles":["T","G"],"end":140541291,"strand":1,"feature_type":"variation","start":140541291,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["G","A"],"end":140541292,"feature_type":"variation","strand":1,"source":"dbSNP","start":140541292,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1303698684","seq_region_name":"7"},{"end":140541294,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140541294,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796647782"},{"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140541296,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541296,"source":"dbSNP","id":"rs1585584282","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140541302,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140541302,"alleles":["A","AA"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs35345826"},{"alleles":["GGGGG","GGGGGG"],"end":140541307,"strand":1,"feature_type":"variation","start":140541303,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1009564041","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140541310,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541310,"clinical_significance":[],"seq_region_name":"7","id":"rs1796648365"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541312,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140541312,"seq_region_name":"7","id":"rs146627224","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541313,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140541313,"seq_region_name":"7","id":"rs906389648","clinical_significance":[]},{"start":140541319,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A","C"],"end":140541319,"strand":1,"feature_type":"variation","id":"rs1002424993","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796648995","clinical_significance":[],"start":140541320,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140541320,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"start":140541321,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140541321,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1033606652","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796649281","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541322,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140541322},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796649413","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140541323,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541323},{"start":140541330,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140541330,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1359208892","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140541340,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541340,"clinical_significance":[],"seq_region_name":"7","id":"rs899041433"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1466877720","feature_type":"variation","strand":1,"end":140541344,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541344},{"clinical_significance":[],"id":"rs1796649839","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541350,"feature_type":"variation","strand":1,"end":140541350,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs112248643","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140541354,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541354},{"strand":1,"feature_type":"variation","end":140541357,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541357,"source":"dbSNP","seq_region_name":"7","id":"rs116515700","clinical_significance":[]},{"seq_region_name":"7","id":"rs1458627708","clinical_significance":[],"start":140541358,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140541358,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1431156611","feature_type":"variation","strand":1,"end":140541360,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541360},{"clinical_significance":[],"id":"rs1796650407","seq_region_name":"7","source":"dbSNP","start":140541361,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140541361,"feature_type":"variation","strand":1},{"end":140541363,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140541363,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs951468507"},{"alleles":["C","T"],"end":140541364,"strand":1,"feature_type":"variation","start":140541364,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796650627","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796650730","clinical_significance":[],"strand":1,"feature_type":"variation","end":140541365,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541365,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1193786890","clinical_significance":[],"alleles":["C","T"],"end":140541366,"strand":1,"feature_type":"variation","start":140541366,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140541368,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541368,"clinical_significance":[],"id":"rs561726628","seq_region_name":"7"},{"end":140541369,"alleles":["AG","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140541368,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs921031425"},{"seq_region_name":"7","id":"rs544175512","clinical_significance":[],"strand":1,"feature_type":"variation","end":140541369,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541369,"source":"dbSNP"},{"source":"dbSNP","start":140541370,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140541370,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796651257"},{"clinical_significance":[],"id":"rs1483447374","seq_region_name":"7","end":140541371,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140541371,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541378,"feature_type":"variation","strand":1,"end":140541378,"alleles":["C","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1796651478"},{"seq_region_name":"7","id":"rs978645207","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541383,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","G","T"],"end":140541383},{"alleles":["C","T"],"end":140541385,"feature_type":"variation","strand":1,"source":"dbSNP","start":140541385,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1796651736","seq_region_name":"7"},{"start":140541386,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140541386,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs1323156581","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796651948","clinical_significance":[],"strand":1,"feature_type":"variation","end":140541387,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541387,"source":"dbSNP"},{"alleles":["C","T"],"end":140541388,"strand":1,"feature_type":"variation","start":140541388,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796652041","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140541391,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541391,"clinical_significance":[],"seq_region_name":"7","id":"rs1278866907"},{"start":140541394,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140541394,"strand":1,"feature_type":"variation","id":"rs965594112","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs111833825","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541395,"source":"dbSNP","strand":1,"feature_type":"variation","end":140541395,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs934634318","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541398,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140541398},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796652353","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541398,"feature_type":"variation","strand":1,"alleles":["CCC","CCCC"],"end":140541400},{"clinical_significance":[],"seq_region_name":"7","id":"rs1404789917","feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140541400,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541400},{"seq_region_name":"7","id":"rs111437630","clinical_significance":[],"end":140541401,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140541401,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796652709","end":140541405,"alleles":["GGGGG","GGGG"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140541401,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs917134806","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541402,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140541402},{"id":"rs1585584573","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140541404,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541404,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541405,"source":"dbSNP","strand":1,"feature_type":"variation","end":140541405,"alleles":["G","A"],"seq_region_name":"7","id":"rs1796652983","clinical_significance":[]},{"id":"rs2130511192","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140541407,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541407,"source":"dbSNP"},{"seq_region_name":"7","id":"rs936916769","clinical_significance":[],"start":140541408,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140541408,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796653179","source":"dbSNP","start":140541409,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140541409,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1170695288","clinical_significance":[],"start":140541411,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140541411,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585584616","alleles":["T","C"],"end":140541412,"feature_type":"variation","strand":1,"source":"dbSNP","start":140541412,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1796653463","clinical_significance":[],"start":140541413,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140541413,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140541415,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541415,"clinical_significance":[],"seq_region_name":"7","id":"rs1796653564"},{"id":"rs1585584631","seq_region_name":"7","clinical_significance":[],"end":140541417,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140541417,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796653747","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140541420,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541420},{"source":"dbSNP","start":140541429,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C","T"],"end":140541429,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs372817874"},{"strand":1,"feature_type":"variation","end":140541434,"alleles":["GGGGGG","GGGGG","GGGGGGG"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541429,"source":"dbSNP","seq_region_name":"7","id":"rs948701440","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140541431,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541431,"source":"dbSNP","seq_region_name":"7","id":"rs1796654130","clinical_significance":[]},{"seq_region_name":"7","id":"rs1192379931","clinical_significance":[],"end":140541432,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140541432,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140541434,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541434,"source":"dbSNP","seq_region_name":"7","id":"rs1796654300","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541435,"feature_type":"variation","strand":1,"end":140541435,"alleles":["T","A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs10952732"},{"source":"dbSNP","start":140541435,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TGC","CGT"],"end":140541437,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs386718481","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1232016191","clinical_significance":[],"alleles":["G","A","T"],"end":140541436,"strand":1,"feature_type":"variation","start":140541436,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1796655076","seq_region_name":"7","source":"dbSNP","start":140541437,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140541437,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs549749459","alleles":["G","A","C"],"end":140541440,"feature_type":"variation","strand":1,"source":"dbSNP","start":140541440,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1279786666","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140541459,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541459,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1796656175","clinical_significance":[],"alleles":["C","T"],"end":140541460,"strand":1,"feature_type":"variation","start":140541460,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs114694379","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541466,"feature_type":"variation","strand":1,"end":140541466,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1461006768","clinical_significance":[],"start":140541468,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140541468,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"alleles":["C","T"],"end":140541469,"strand":1,"feature_type":"variation","start":140541469,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796656485","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["CAG","CAGCAG"],"end":140541473,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541471,"clinical_significance":[],"id":"rs1796656593","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541475,"source":"dbSNP","strand":1,"feature_type":"variation","end":140541475,"alleles":["C","A"],"seq_region_name":"7","id":"rs995314640","clinical_significance":[]},{"end":140541476,"alleles":["CC","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140541475,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796656837"},{"clinical_significance":[],"id":"rs1200541637","seq_region_name":"7","source":"dbSNP","start":140541486,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A","G"],"end":140541486,"feature_type":"variation","strand":1},{"id":"rs945014095","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541489,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140541489},{"alleles":["TTTT","TTT"],"end":140541496,"strand":1,"feature_type":"variation","start":140541493,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796657192","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140541496,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541496,"clinical_significance":[],"seq_region_name":"7","id":"rs1796657285"},{"end":140541497,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140541497,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796657385"},{"source":"dbSNP","start":140541501,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140541501,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585584798"},{"clinical_significance":[],"id":"rs529241855","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541503,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140541503},{"id":"rs1047934384","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140541505,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541505,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140541506,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541506,"clinical_significance":[],"seq_region_name":"7","id":"rs1046148862"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1310981995","alleles":["A","C"],"end":140541507,"feature_type":"variation","strand":1,"source":"dbSNP","start":140541507,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140541508,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140541508,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs547697649"},{"source":"dbSNP","start":140541509,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140541509,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1404830613","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1331595622","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541510,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140541510},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541512,"feature_type":"variation","strand":1,"end":140541512,"alleles":["C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1464823976"},{"seq_region_name":"7","id":"rs2130511552","clinical_significance":[],"start":140541520,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140541520,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140541526,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541526,"clinical_significance":[],"seq_region_name":"7","id":"rs927676942"},{"clinical_significance":[],"id":"rs1393654709","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541532,"feature_type":"variation","strand":1,"end":140541532,"alleles":["C","G"]},{"strand":1,"feature_type":"variation","alleles":["G","C","T"],"end":140541535,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541535,"source":"dbSNP","seq_region_name":"7","id":"rs937864623","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs79124773","feature_type":"variation","strand":1,"end":140541536,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541536},{"clinical_significance":[],"seq_region_name":"7","id":"rs900741042","source":"dbSNP","start":140541537,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140541537,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1796658876","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541540,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140541540},{"seq_region_name":"7","id":"rs1796658971","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541541,"source":"dbSNP","strand":1,"feature_type":"variation","end":140541541,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796659049","end":140541548,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140541548,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1238622337","source":"dbSNP","start":140541549,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A","G"],"end":140541549,"feature_type":"variation","strand":1},{"alleles":["G","A","C"],"end":140541550,"strand":1,"feature_type":"variation","start":140541550,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs768976142","clinical_significance":[]},{"source":"dbSNP","start":140541554,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140541554,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs2130511660","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140541558,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541558,"clinical_significance":[],"id":"rs1456639418","seq_region_name":"7"},{"start":140541559,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140541559,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585584917","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541568,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140541568,"clinical_significance":[],"id":"rs1796659737","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140541575,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541575,"clinical_significance":[],"seq_region_name":"7","id":"rs1796659873"},{"seq_region_name":"7","id":"rs2130511692","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541576,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140541576},{"seq_region_name":"7","id":"rs1198352925","clinical_significance":[],"alleles":["T","TT"],"end":140541578,"strand":1,"feature_type":"variation","start":140541578,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541578,"source":"dbSNP","strand":1,"feature_type":"variation","end":140541578,"alleles":["T","C"],"seq_region_name":"7","id":"rs1210547908","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs539590369","feature_type":"variation","strand":1,"end":140541579,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541579},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541583,"source":"dbSNP","strand":1,"feature_type":"variation","end":140541583,"alleles":["T","C"],"seq_region_name":"7","id":"rs145195331","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541588,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140541588,"clinical_significance":[],"seq_region_name":"7","id":"rs1796660318"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140541592,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541592,"clinical_significance":[],"seq_region_name":"7","id":"rs1156661190"},{"seq_region_name":"7","id":"rs1187841795","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541593,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140541593},{"source":"dbSNP","start":140541595,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140541595,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796661251"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541596,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140541596,"seq_region_name":"7","id":"rs137903186","clinical_significance":[]},{"id":"rs111288105","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140541597,"strand":1,"feature_type":"variation","start":140541597,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140541600,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541600,"source":"dbSNP","seq_region_name":"7","id":"rs1448506118","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140541605,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541605,"clinical_significance":[],"seq_region_name":"7","id":"rs968519548"},{"clinical_significance":[],"seq_region_name":"7","id":"rs978916049","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541611,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140541611},{"strand":1,"feature_type":"variation","end":140541612,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541612,"source":"dbSNP","id":"rs1405447369","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1392718839","clinical_significance":[],"start":140541613,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140541613,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1796662192","clinical_significance":[],"start":140541614,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140541614,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1161578721","alleles":["A","C"],"end":140541618,"feature_type":"variation","strand":1,"source":"dbSNP","start":140541618,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140541619,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140541619,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1031537378","clinical_significance":[]},{"alleles":["T","G"],"end":140541623,"strand":1,"feature_type":"variation","start":140541623,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs180877117","clinical_significance":[]},{"id":"rs992619507","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140541626,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541626,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1438021986","clinical_significance":[],"strand":1,"feature_type":"variation","end":140541629,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541629,"source":"dbSNP"},{"alleles":["G","T"],"end":140541631,"feature_type":"variation","strand":1,"source":"dbSNP","start":140541631,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796662854"},{"id":"rs1796662953","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140541632,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541632,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541635,"feature_type":"variation","strand":1,"end":140541636,"alleles":["CC","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1796663058"},{"start":140541636,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140541636,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796663160","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140541638,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541638,"clinical_significance":[],"seq_region_name":"7","id":"rs1387878970"},{"seq_region_name":"7","id":"rs917188476","clinical_significance":[],"start":140541639,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140541639,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796663460","end":140541640,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140541640,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1199602423","source":"dbSNP","start":140541641,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140541641,"alleles":["C","G"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140541643,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541643,"source":"dbSNP","seq_region_name":"7","id":"rs1796663628","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796663731","clinical_significance":[],"start":140541645,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140541656,"alleles":["AACCTTGAGAAC","AAC"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1453392672","source":"dbSNP","start":140541646,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140541646,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs75834410","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140541647,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541647},{"id":"rs1222360710","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541650,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140541650},{"id":"rs1796664062","seq_region_name":"7","clinical_significance":[],"end":140541652,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140541652,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140541662,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140541662,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796664164"},{"end":140541663,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140541663,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796664262"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796664371","alleles":["T","-"],"end":140541666,"feature_type":"variation","strand":1,"source":"dbSNP","start":140541666,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["A","G","T"],"end":140541669,"strand":1,"feature_type":"variation","start":140541669,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1355106789","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1288538023","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541670,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140541670},{"end":140541700,"alleles":["TCCCCAGTGCCCGGGAGCTTGGAGAGCTCC","TCCCCAGTGCCCGGGAGCTTGGAGAGCTCCCCAGTGCCCGGGAGCTTGGAGAGCTCC"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140541671,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796664721"},{"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140541672,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541672,"source":"dbSNP","seq_region_name":"7","id":"rs1238469735","clinical_significance":[]},{"id":"rs1348015541","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140541680,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541680,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1278604156","clinical_significance":[],"start":140541682,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140541682,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140541683,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541683,"source":"dbSNP","seq_region_name":"7","id":"rs573689759","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796665308","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541685,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140541685},{"clinical_significance":[],"id":"rs1796665413","seq_region_name":"7","alleles":["C","G"],"end":140541688,"feature_type":"variation","strand":1,"source":"dbSNP","start":140541688,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140541689,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541689,"source":"dbSNP","seq_region_name":"7","id":"rs1019714068","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796665631","clinical_significance":[],"strand":1,"feature_type":"variation","end":140541691,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541691,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541696,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140541696,"clinical_significance":[],"seq_region_name":"7","id":"rs141682355"},{"source":"dbSNP","start":140541700,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140541700,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1332313192"},{"source":"dbSNP","start":140541702,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140541718,"alleles":["CAGCGCCCAGCACCAGC","CAGCGCCCAGCACCAGCGCCCAGCGCCCAGCACCAGC"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1796666029","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541705,"feature_type":"variation","strand":1,"end":140541705,"alleles":["C","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1563127077"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1351933152","source":"dbSNP","start":140541706,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140541706,"alleles":["G","A"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541709,"source":"dbSNP","strand":1,"feature_type":"variation","end":140541709,"alleles":["C","A","T"],"seq_region_name":"7","id":"rs980124020","clinical_significance":[]},{"clinical_significance":[],"id":"rs1404230338","seq_region_name":"7","end":140541716,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140541716,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140541717,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541717,"clinical_significance":[],"id":"rs1286815056","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541720,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140541720,"clinical_significance":[],"id":"rs1328940715","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1361129004","seq_region_name":"7","alleles":["CAA","-"],"end":140541723,"feature_type":"variation","strand":1,"source":"dbSNP","start":140541721,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140541725,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140541725,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs762253728","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541729,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140541729,"clinical_significance":[],"seq_region_name":"7","id":"rs1430458593"},{"feature_type":"variation","strand":1,"end":140541730,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541730,"clinical_significance":[],"seq_region_name":"7","id":"rs1796667272"},{"alleles":["A","G"],"end":140541731,"strand":1,"feature_type":"variation","start":140541731,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1160170504","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541732,"feature_type":"variation","strand":1,"end":140541732,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs752964976"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1398755265","source":"dbSNP","start":140541735,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["-","CTGCA"],"end":140541734,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1796667719","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541735,"source":"dbSNP","strand":1,"feature_type":"variation","end":140541739,"alleles":["AGGGC","-"]},{"seq_region_name":"7","id":"rs2130512221","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140541736,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541736,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1407057546","seq_region_name":"7","feature_type":"variation","strand":1,"end":140541742,"alleles":["GGCCTG","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541737},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541739,"source":"dbSNP","strand":1,"feature_type":"variation","end":140541739,"alleles":["C","T"],"seq_region_name":"7","id":"rs1796667953","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs553611279","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140541740,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541740},{"strand":1,"feature_type":"variation","end":140541741,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541741,"source":"dbSNP","seq_region_name":"7","id":"rs578126935","clinical_significance":[]},{"clinical_significance":[],"id":"rs920591228","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541742,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140541742},{"feature_type":"variation","strand":1,"end":140541743,"alleles":["GC","GCAAGGC"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541742,"clinical_significance":[],"id":"rs1796668431","seq_region_name":"7"},{"start":140541748,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140541748,"strand":1,"feature_type":"variation","id":"rs1479152968","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1427264618","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140541749,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541749},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541756,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140541756,"clinical_significance":[],"seq_region_name":"7","id":"rs1198819313"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796668866","source":"dbSNP","start":140541758,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140541758,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs930781325","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541766,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140541766},{"id":"rs965809437","seq_region_name":"7","clinical_significance":[],"end":140541767,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140541767,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["G","A","C","T"],"end":140541768,"strand":1,"feature_type":"variation","start":140541768,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs185282758","clinical_significance":[]},{"end":140541769,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140541769,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1028890853"},{"seq_region_name":"7","id":"rs1796669538","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140541771,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541771,"source":"dbSNP"},{"alleles":["A","G"],"end":140541774,"strand":1,"feature_type":"variation","start":140541774,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs958344106","clinical_significance":[]},{"id":"rs1796669769","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541775,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140541775},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140541776,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541776,"source":"dbSNP","seq_region_name":"7","id":"rs17161629","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140541778,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541778,"source":"dbSNP","id":"rs996364597","seq_region_name":"7","clinical_significance":[]},{"id":"rs1209310626","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140541781,"strand":1,"feature_type":"variation","start":140541781,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1251401552","alleles":["G","T"],"end":140541782,"feature_type":"variation","strand":1,"source":"dbSNP","start":140541782,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1299950012","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140541796,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541796,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140541800,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541800,"clinical_significance":[],"id":"rs1796670756","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541801,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140541801,"clinical_significance":[],"seq_region_name":"7","id":"rs914130643"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541804,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140541804,"seq_region_name":"7","id":"rs1796670985","clinical_significance":[]},{"source":"dbSNP","start":140541805,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140541805,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1344355438","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796671227","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541809,"feature_type":"variation","strand":1,"alleles":["TAAA","TAAATAAA"],"end":140541812},{"id":"rs1027982993","seq_region_name":"7","clinical_significance":[],"start":140541813,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140541817,"alleles":["ACACA","ACA"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1404225508","source":"dbSNP","start":140541818,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["GGG","GG"],"end":140541820,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140541819,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140541819,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs773745522"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541820,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140541820,"seq_region_name":"7","id":"rs1796671573","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796671679","end":140541821,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140541821,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140541822,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541822,"clinical_significance":[],"seq_region_name":"7","id":"rs1796671770"},{"strand":1,"feature_type":"variation","end":140541824,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541824,"source":"dbSNP","id":"rs904177398","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1410890306","feature_type":"variation","strand":1,"alleles":["GGGAACAGCCAGATGG","G"],"end":140541848,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541833},{"clinical_significance":[],"seq_region_name":"7","id":"rs1185280902","source":"dbSNP","start":140541835,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140541835,"alleles":["G","C"],"feature_type":"variation","strand":1},{"alleles":["C","T"],"end":140541838,"strand":1,"feature_type":"variation","start":140541838,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1475396048","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796672350","clinical_significance":[],"strand":1,"feature_type":"variation","end":140541840,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541840,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1796672453","clinical_significance":[],"end":140541846,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140541846,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1796672571","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541852,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140541852},{"clinical_significance":[],"id":"rs528927396","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140541854,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541854},{"start":140541856,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140541856,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1238383994","clinical_significance":[]},{"alleles":["A","G"],"end":140541860,"feature_type":"variation","strand":1,"source":"dbSNP","start":140541860,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1796672907","seq_region_name":"7"},{"alleles":["GG","G"],"end":140541864,"strand":1,"feature_type":"variation","start":140541863,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130512578","clinical_significance":[]},{"source":"dbSNP","start":140541863,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["GGTGCATCAGAAAGGTGACCAGATGCGG","GG"],"end":140541890,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1212705573"},{"seq_region_name":"7","id":"rs2130512594","clinical_significance":[],"strand":1,"feature_type":"variation","end":140541864,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541864,"source":"dbSNP"},{"id":"rs999830775","seq_region_name":"7","clinical_significance":[],"end":140541865,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140541865,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs188734730","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541876,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140541876},{"seq_region_name":"7","id":"rs927766828","clinical_significance":[],"start":140541883,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140541883,"strand":1,"feature_type":"variation"},{"start":140541886,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140541886,"alleles":["T","C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1317999913","clinical_significance":[]},{"id":"rs1279588472","seq_region_name":"7","clinical_significance":[],"end":140541888,"alleles":["C","A","G","T"],"strand":1,"feature_type":"variation","start":140541888,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs955791446","end":140541889,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140541889,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541890,"source":"dbSNP","strand":1,"feature_type":"variation","end":140541890,"alleles":["G","C"],"seq_region_name":"7","id":"rs73487649","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1024127510","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541891,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140541891},{"start":140541892,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140541892,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","id":"rs150122332","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140541894,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541894,"source":"dbSNP","id":"rs1796674586","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1054992775","source":"dbSNP","start":140541895,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140541895,"alleles":["T","A","G"],"feature_type":"variation","strand":1},{"alleles":["GAG","GAGAG"],"end":140541898,"feature_type":"variation","strand":1,"source":"dbSNP","start":140541896,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1298226737"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541901,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140541901,"id":"rs1409843929","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140541905,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541905,"clinical_significance":[],"seq_region_name":"7","id":"rs1796675200"},{"seq_region_name":"7","id":"rs1796675349","clinical_significance":[],"alleles":["G","A"],"end":140541906,"strand":1,"feature_type":"variation","start":140541906,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140541914,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140541914,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1415193272"},{"alleles":["G","A"],"end":140541915,"strand":1,"feature_type":"variation","start":140541915,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs75863541","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585585671","clinical_significance":[],"alleles":["T","C"],"end":140541918,"strand":1,"feature_type":"variation","start":140541918,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs980008313","clinical_significance":[],"alleles":["C","T"],"end":140541919,"strand":1,"feature_type":"variation","start":140541919,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541921,"source":"dbSNP","strand":1,"feature_type":"variation","end":140541921,"alleles":["C","A","G","T"],"seq_region_name":"7","id":"rs867408745","clinical_significance":[]},{"seq_region_name":"7","id":"rs920489460","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541922,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140541922},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541924,"source":"dbSNP","strand":1,"feature_type":"variation","end":140541924,"alleles":["C","T"],"seq_region_name":"7","id":"rs1796676203","clinical_significance":[]},{"alleles":["C","G","T"],"end":140541926,"strand":1,"feature_type":"variation","start":140541926,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1796676364","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796676551","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140541928,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541928},{"start":140541929,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140541929,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs930436484","clinical_significance":[]},{"id":"rs1201864096","seq_region_name":"7","clinical_significance":[],"start":140541937,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C"],"end":140541937,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140541939,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541939,"source":"dbSNP","seq_region_name":"7","id":"rs1796677072","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140541940,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541940,"source":"dbSNP","seq_region_name":"7","id":"rs370044858","clinical_significance":[]},{"start":140541942,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140541942,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs374426350","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796677581","end":140541943,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140541943,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1796677724","clinical_significance":[],"strand":1,"feature_type":"variation","end":140541950,"alleles":["A","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541950,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1306783033","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","-"],"end":140541951,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541951,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1796677918","clinical_significance":[],"start":140541951,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140541951,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"start":140541952,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140541952,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs751529794","clinical_significance":[]},{"seq_region_name":"7","id":"rs547735515","clinical_significance":[],"strand":1,"feature_type":"variation","end":140541956,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541956,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140541962,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541962,"source":"dbSNP","id":"rs1796678569","seq_region_name":"7","clinical_significance":[]},{"start":140541963,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140541963,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs377413454","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796678884","alleles":["A","G"],"end":140541968,"feature_type":"variation","strand":1,"source":"dbSNP","start":140541968,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140541973,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541973,"source":"dbSNP","id":"rs1796678977","seq_region_name":"7","clinical_significance":[]},{"id":"rs1040541875","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140541974,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541974,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1796679189","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541975,"source":"dbSNP","strand":1,"feature_type":"variation","end":140541975,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs900674238","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541976,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140541976},{"seq_region_name":"7","id":"rs1447761476","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140541977,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541977,"source":"dbSNP"},{"end":140541979,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140541979,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1350189091"},{"id":"rs932268351","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140541989,"alleles":["TTTTTTTTT","TTTTTT","TTTTTTTT","TTTTTTTTTT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140541981,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1796679941","clinical_significance":[],"start":140541984,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140541984,"strand":1,"feature_type":"variation"},{"start":140541989,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140541989,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs77033910","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140541994,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140541994,"clinical_significance":[],"id":"rs1350601643","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1796680302","seq_region_name":"7","source":"dbSNP","start":140541996,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140541996,"alleles":["C","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1167528168","end":140542008,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140542008,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["G","C","T"],"end":140542011,"strand":1,"feature_type":"variation","start":140542011,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1315352309","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542013,"source":"dbSNP","strand":1,"feature_type":"variation","end":140542013,"alleles":["T","G"],"seq_region_name":"7","id":"rs904065422","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542014,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140542014,"seq_region_name":"7","id":"rs1796681014","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542019,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140542019,"seq_region_name":"7","id":"rs1796681159","clinical_significance":[]},{"seq_region_name":"7","id":"rs901281406","clinical_significance":[],"start":140542020,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140542020,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1796681465","clinical_significance":[],"strand":1,"feature_type":"variation","end":140542023,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542023,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1320424803","seq_region_name":"7","feature_type":"variation","strand":1,"end":140542025,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542025},{"clinical_significance":[],"seq_region_name":"7","id":"rs997325812","source":"dbSNP","start":140542027,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140542027,"alleles":["C","T"],"feature_type":"variation","strand":1},{"start":140542028,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140542028,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs866259573","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140542033,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542033,"clinical_significance":[],"id":"rs1796682085","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1028377877","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542040,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140542040},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140542041,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542041,"clinical_significance":[],"seq_region_name":"7","id":"rs1796682399"},{"clinical_significance":[],"seq_region_name":"7","id":"rs763929478","alleles":["G","A"],"end":140542044,"feature_type":"variation","strand":1,"source":"dbSNP","start":140542044,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542049,"source":"dbSNP","strand":1,"feature_type":"variation","end":140542049,"alleles":["A","C"],"seq_region_name":"7","id":"rs1344441333","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140542050,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542050,"clinical_significance":[],"id":"rs1203214774","seq_region_name":"7"},{"end":140542052,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140542052,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs367661376"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542052,"source":"dbSNP","strand":1,"feature_type":"variation","end":140542060,"alleles":["TTTTTTTTT","TTTTTTTT","TTTTTTTTTT"],"seq_region_name":"7","id":"rs1052757712","clinical_significance":[]},{"end":140542058,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140542058,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796683568","clinical_significance":[]},{"alleles":["T","C"],"end":140542059,"strand":1,"feature_type":"variation","start":140542059,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585586053","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1246851399","alleles":["T","C","G"],"end":140542060,"feature_type":"variation","strand":1,"source":"dbSNP","start":140542060,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140542061,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140542061,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1183368062","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140542067,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542067,"source":"dbSNP","seq_region_name":"7","id":"rs1253873804","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1014011936","alleles":["A","G"],"end":140542070,"feature_type":"variation","strand":1,"source":"dbSNP","start":140542070,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140542079,"alleles":["TGCTTCTT","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542072,"source":"dbSNP","seq_region_name":"7","id":"rs1171095066","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1391426200","alleles":["T","A"],"end":140542075,"feature_type":"variation","strand":1,"source":"dbSNP","start":140542075,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs181481205","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140542082,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542082},{"seq_region_name":"7","id":"rs1167494751","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542085,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140542085},{"seq_region_name":"7","id":"rs1391108909","clinical_significance":[],"end":140542086,"alleles":["T","C","G"],"strand":1,"feature_type":"variation","start":140542086,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["C","T"],"end":140542095,"strand":1,"feature_type":"variation","start":140542095,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1796685353","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1295416920","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542096,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140542096},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140542097,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542097,"clinical_significance":[],"id":"rs1796685616","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1021168442","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542102,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140542102},{"clinical_significance":[],"seq_region_name":"7","id":"rs966924114","source":"dbSNP","start":140542103,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140542103,"alleles":["C","T"],"feature_type":"variation","strand":1},{"end":140542105,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140542105,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs981779860"},{"seq_region_name":"7","id":"rs1304932174","clinical_significance":[],"end":140542106,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140542106,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1796686314","seq_region_name":"7","feature_type":"variation","strand":1,"end":140542107,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542107},{"id":"rs1796686468","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140542108,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542108,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1299114785","clinical_significance":[],"start":140542111,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140542111,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"end":140542113,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140542113,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs927603949"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542115,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140542115,"id":"rs1585586219","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796687011","source":"dbSNP","start":140542116,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140542116,"feature_type":"variation","strand":1},{"start":140542117,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140542117,"alleles":["C","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796687146","clinical_significance":[]},{"clinical_significance":[],"id":"rs116462089","seq_region_name":"7","end":140542118,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140542118,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140542119,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542119,"source":"dbSNP","seq_region_name":"7","id":"rs1028005143","clinical_significance":[]},{"alleles":["T","G"],"end":140542122,"feature_type":"variation","strand":1,"source":"dbSNP","start":140542122,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796687582"},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140542124,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542124,"clinical_significance":[],"id":"rs370120153","seq_region_name":"7"},{"end":140542125,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140542125,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796687809","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796687972","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542126,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140542126},{"seq_region_name":"7","id":"rs1796688126","clinical_significance":[],"start":140542128,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140542128,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1425226571","clinical_significance":[],"strand":1,"feature_type":"variation","end":140542131,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542131,"source":"dbSNP"},{"alleles":["C","G"],"end":140542132,"feature_type":"variation","strand":1,"source":"dbSNP","start":140542132,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1200980591"},{"source":"dbSNP","start":140542133,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140542133,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1489827269","seq_region_name":"7"},{"end":140542137,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140542137,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs990991458","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140542142,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542142,"clinical_significance":[],"seq_region_name":"7","id":"rs920335613"},{"feature_type":"variation","strand":1,"end":140542143,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542143,"clinical_significance":[],"seq_region_name":"7","id":"rs757011585"},{"clinical_significance":[],"seq_region_name":"7","id":"rs983249318","alleles":["C","T"],"end":140542147,"feature_type":"variation","strand":1,"source":"dbSNP","start":140542147,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs537190102","feature_type":"variation","strand":1,"end":140542148,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542148},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140542152,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542152,"clinical_significance":[],"seq_region_name":"7","id":"rs1796689389"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542156,"source":"dbSNP","strand":1,"feature_type":"variation","end":140542156,"alleles":["G","C"],"seq_region_name":"7","id":"rs1428586079","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796689722","clinical_significance":[],"start":140542167,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140542167,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs545485221","clinical_significance":[],"strand":1,"feature_type":"variation","end":140542172,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542172,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs778636463","end":140542173,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140542173,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140542174,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140542174,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs907826322"},{"alleles":["G","A"],"end":140542179,"strand":1,"feature_type":"variation","start":140542179,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796690377","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs555427917","source":"dbSNP","start":140542180,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140542180,"feature_type":"variation","strand":1},{"id":"rs1285227851","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140542182,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542182,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542182,"source":"dbSNP","strand":1,"feature_type":"variation","end":140542186,"alleles":["CCCCC","CCCCCC"],"seq_region_name":"7","id":"rs1226270202","clinical_significance":[]},{"seq_region_name":"7","id":"rs944603899","clinical_significance":[],"alleles":["C","T"],"end":140542186,"strand":1,"feature_type":"variation","start":140542186,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["G","T"],"end":140542188,"strand":1,"feature_type":"variation","start":140542188,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1796691152","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1796691280","seq_region_name":"7","source":"dbSNP","start":140542189,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140542189,"feature_type":"variation","strand":1},{"alleles":["A","C"],"end":140542193,"strand":1,"feature_type":"variation","start":140542193,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1345371335","seq_region_name":"7","clinical_significance":[]},{"id":"rs1796691506","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542195,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140542195},{"clinical_significance":[],"id":"rs1041080778","seq_region_name":"7","source":"dbSNP","start":140542206,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140542206,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs567353607","source":"dbSNP","start":140542207,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140542207,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs901182136","clinical_significance":[],"strand":1,"feature_type":"variation","end":140542208,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542208,"source":"dbSNP"},{"source":"dbSNP","start":140542209,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140542209,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1312970872","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542218,"source":"dbSNP","strand":1,"feature_type":"variation","end":140542218,"alleles":["A","G"],"seq_region_name":"7","id":"rs750237506","clinical_significance":[]},{"alleles":["T","G"],"end":140542220,"strand":1,"feature_type":"variation","start":140542220,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1383219246","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140542225,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542225,"clinical_significance":[],"seq_region_name":"7","id":"rs2130513669"},{"clinical_significance":[],"seq_region_name":"7","id":"rs757928655","feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140542229,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542229},{"end":140542231,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140542231,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796692550","clinical_significance":[]},{"clinical_significance":[],"id":"rs1359409123","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140542234,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542234},{"clinical_significance":[],"seq_region_name":"7","id":"rs1177880726","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140542236,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542236},{"seq_region_name":"7","id":"rs1563127433","clinical_significance":[],"strand":1,"feature_type":"variation","end":140542240,"alleles":["TTTTT","TTTT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542236,"source":"dbSNP"},{"source":"dbSNP","start":140542237,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140542237,"alleles":["T","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1479176328"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140542240,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542240,"source":"dbSNP","id":"rs1796693127","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796693226","clinical_significance":[],"end":140542245,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140542245,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs534672127","clinical_significance":[],"start":140542246,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140542246,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796693441","alleles":["C","T"],"end":140542248,"feature_type":"variation","strand":1,"source":"dbSNP","start":140542248,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542252,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140542252,"seq_region_name":"7","id":"rs1482817832","clinical_significance":[]},{"start":140542253,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140542253,"strand":1,"feature_type":"variation","id":"rs976128679","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140542254,"alleles":["G","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542254,"clinical_significance":[],"seq_region_name":"7","id":"rs1796693753"},{"start":140542257,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140542257,"strand":1,"feature_type":"variation","id":"rs1796693935","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796694030","clinical_significance":[],"end":140542259,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140542259,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1430292968","clinical_significance":[],"start":140542261,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140542261,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1796694215","clinical_significance":[],"end":140542262,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140542262,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["C","G"],"end":140542264,"feature_type":"variation","strand":1,"source":"dbSNP","start":140542264,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585586548"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542271,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140542271,"id":"rs893856577","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542272,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C","T"],"end":140542272,"seq_region_name":"7","id":"rs66736733","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140542277,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542277,"source":"dbSNP","seq_region_name":"7","id":"rs1796694841","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796695016","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542278,"source":"dbSNP","strand":1,"feature_type":"variation","end":140542278,"alleles":["C","T"]},{"end":140542280,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140542280,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796695171"},{"end":140542283,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140542283,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1249817743"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1021073617","source":"dbSNP","start":140542284,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140542284,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1457535360","feature_type":"variation","strand":1,"end":140542285,"alleles":["GG","GGG"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542284},{"feature_type":"variation","strand":1,"end":140542285,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542285,"clinical_significance":[],"seq_region_name":"7","id":"rs902795010"},{"start":140542287,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TCTTCTT","TCTT"],"end":140542293,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796695920","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796696021","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["TTT","-"],"end":140542294,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542292,"source":"dbSNP"},{"end":140542296,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140542296,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1003740651","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1043876502","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542299,"feature_type":"variation","strand":1,"end":140542299,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1278959841","clinical_significance":[],"start":140542300,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140542300,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs578159983","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140542304,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542304},{"seq_region_name":"7","id":"rs1325220377","clinical_significance":[],"end":140542305,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140542305,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1796696623","clinical_significance":[],"start":140542305,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","-"],"end":140542305,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796696712","source":"dbSNP","start":140542306,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140542306,"alleles":["T","C"],"feature_type":"variation","strand":1},{"end":140542307,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140542307,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs959318246"},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140542309,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542309,"source":"dbSNP","seq_region_name":"7","id":"rs1295247868","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542317,"source":"dbSNP","strand":1,"feature_type":"variation","end":140542317,"alleles":["A","C"],"seq_region_name":"7","id":"rs1796697005","clinical_significance":[]},{"seq_region_name":"7","id":"rs112519311","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542319,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140542319},{"alleles":["T","C"],"end":140542322,"feature_type":"variation","strand":1,"source":"dbSNP","start":140542322,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1187371209"},{"clinical_significance":[],"id":"rs1338292252","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542333,"feature_type":"variation","strand":1,"end":140542333,"alleles":["C","G"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542336,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140542336,"seq_region_name":"7","id":"rs1796697439","clinical_significance":[]},{"start":140542339,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140542339,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796697546","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140542341,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542341,"source":"dbSNP","seq_region_name":"7","id":"rs1027826001","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796697787","source":"dbSNP","start":140542341,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140542341,"alleles":["C","-"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542342,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140542342,"id":"rs1170801566","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","A"],"end":140542344,"feature_type":"variation","strand":1,"source":"dbSNP","start":140542344,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1463426960"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542346,"feature_type":"variation","strand":1,"end":140542346,"alleles":["G","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1796698085"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542354,"feature_type":"variation","strand":1,"end":140542354,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1053238308"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542356,"source":"dbSNP","strand":1,"feature_type":"variation","end":140542356,"alleles":["A","G"],"seq_region_name":"7","id":"rs1796698289","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1192132760","alleles":["G","A"],"end":140542359,"feature_type":"variation","strand":1,"source":"dbSNP","start":140542359,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140542361,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542361,"source":"dbSNP","seq_region_name":"7","id":"rs1796698492","clinical_significance":[]},{"source":"dbSNP","start":140542362,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140542362,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130514110"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542363,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140542363,"clinical_significance":[],"seq_region_name":"7","id":"rs1424164408"},{"end":140542369,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140542369,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1395203793","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542372,"source":"dbSNP","strand":1,"feature_type":"variation","end":140542372,"alleles":["G","A","C"],"seq_region_name":"7","id":"rs768270463","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796698905","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140542373,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542373,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140542388,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542388,"source":"dbSNP","seq_region_name":"7","id":"rs1434507396","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs951769139","source":"dbSNP","start":140542389,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140542389,"feature_type":"variation","strand":1},{"start":140542390,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140542390,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs1796699204","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140542399,"alleles":["TTTGCTTT","TTT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542392,"clinical_significance":[],"seq_region_name":"7","id":"rs1796699345"},{"clinical_significance":[],"seq_region_name":"7","id":"rs983323618","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542395,"feature_type":"variation","strand":1,"end":140542395,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs557570366","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140542402,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542402},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542403,"feature_type":"variation","strand":1,"end":140542403,"alleles":["G","A"],"clinical_significance":[],"id":"rs1796699680","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs907696492","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140542406,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542406},{"clinical_significance":[],"seq_region_name":"7","id":"rs1045510781","alleles":["G","A","T"],"end":140542409,"feature_type":"variation","strand":1,"source":"dbSNP","start":140542409,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542413,"source":"dbSNP","strand":1,"feature_type":"variation","end":140542413,"alleles":["G","T"],"id":"rs1796700189","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796700344","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542413,"feature_type":"variation","strand":1,"alleles":["GATGCCCTCACGATG","GATG"],"end":140542427},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542415,"feature_type":"variation","strand":1,"end":140542415,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs575888828"},{"start":140542419,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140542419,"strand":1,"feature_type":"variation","id":"rs1796700620","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542424,"source":"dbSNP","strand":1,"feature_type":"variation","end":140542424,"alleles":["G","A","T"],"seq_region_name":"7","id":"rs1796700791","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130514273","source":"dbSNP","start":140542425,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140542425,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796700990","source":"dbSNP","start":140542428,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140542428,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs905589990","end":140542435,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140542435,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140542442,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140542442,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796701331"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140542450,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542450,"clinical_significance":[],"seq_region_name":"7","id":"rs1001790216"},{"seq_region_name":"7","id":"rs1796701631","clinical_significance":[],"strand":1,"feature_type":"variation","end":140542451,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542451,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796701782","alleles":["T","A"],"end":140542461,"feature_type":"variation","strand":1,"source":"dbSNP","start":140542461,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1381631918","clinical_significance":[],"start":140542466,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140542466,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"start":140542467,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140542467,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1328869721","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140542470,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542470,"clinical_significance":[],"id":"rs1796702177","seq_region_name":"7"},{"id":"rs1392640109","seq_region_name":"7","clinical_significance":[],"start":140542471,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140542471,"strand":1,"feature_type":"variation"},{"alleles":["C","T"],"end":140542472,"strand":1,"feature_type":"variation","start":140542472,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796702457","clinical_significance":[]},{"clinical_significance":[],"id":"rs1796702624","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140542473,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542473},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796702770","feature_type":"variation","strand":1,"end":140542476,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542476},{"id":"rs1465859464","seq_region_name":"7","clinical_significance":[],"start":140542479,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140542479,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796703017","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542479,"feature_type":"variation","strand":1,"end":140542481,"alleles":["CAC","C"]},{"seq_region_name":"7","id":"rs1796703128","clinical_significance":[],"strand":1,"feature_type":"variation","end":140542482,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542482,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1167258790","source":"dbSNP","start":140542483,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140542483,"alleles":["A","G"],"feature_type":"variation","strand":1},{"end":140542485,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140542485,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs56845124","clinical_significance":[]},{"seq_region_name":"7","id":"rs781241802","clinical_significance":[],"strand":1,"feature_type":"variation","end":140542488,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542488,"source":"dbSNP"},{"seq_region_name":"7","id":"rs6978044","clinical_significance":[],"end":140542489,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140542489,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140542495,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140542495,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130514448"},{"seq_region_name":"7","id":"rs1239021864","clinical_significance":[],"alleles":["T","C"],"end":140542497,"strand":1,"feature_type":"variation","start":140542497,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542501,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140542501,"clinical_significance":[],"seq_region_name":"7","id":"rs1184004634"},{"start":140542502,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140542502,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs1436137873","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs6955257","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140542504,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542504,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs868692976","end":140542506,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140542506,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1368434697","clinical_significance":[],"start":140542507,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140542507,"strand":1,"feature_type":"variation"},{"start":140542508,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","G","T"],"end":140542508,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs138163361","clinical_significance":[]},{"alleles":["TTCCTCTCTCTGGGCCAGCCCT","-"],"end":140542533,"feature_type":"variation","strand":1,"source":"dbSNP","start":140542512,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796704814"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1279758089","feature_type":"variation","strand":1,"alleles":["CTCTCTCT","CTCTCT"],"end":140542522,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542515},{"start":140542523,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140542523,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796705034","clinical_significance":[]},{"source":"dbSNP","start":140542525,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140542525,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1299481148"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140542527,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542527,"source":"dbSNP","id":"rs1796705240","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140542528,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542528,"clinical_significance":[],"seq_region_name":"7","id":"rs1333443750"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1311321821","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542530,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140542530},{"end":140542531,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140542531,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796705556","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796705659","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542532,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140542532},{"strand":1,"feature_type":"variation","end":140542533,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542533,"source":"dbSNP","seq_region_name":"7","id":"rs953434223","clinical_significance":[]},{"seq_region_name":"7","id":"rs1297473026","clinical_significance":[],"alleles":["A","G"],"end":140542534,"strand":1,"feature_type":"variation","start":140542534,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796705960","alleles":["G","A"],"end":140542535,"feature_type":"variation","strand":1,"source":"dbSNP","start":140542535,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542537,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140542537,"id":"rs2130514620","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1405429210","clinical_significance":[],"start":140542538,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140542538,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542540,"feature_type":"variation","strand":1,"end":140542540,"alleles":["C","T"],"clinical_significance":[],"id":"rs893929987","seq_region_name":"7"},{"id":"rs1796706334","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140542542,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542542,"source":"dbSNP"},{"end":140542549,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140542549,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585587038","clinical_significance":[]},{"seq_region_name":"7","id":"rs946781567","clinical_significance":[],"strand":1,"feature_type":"variation","end":140542554,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542554,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140542558,"alleles":["TTTTT","TTT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542554,"clinical_significance":[],"seq_region_name":"7","id":"rs1796706627"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542557,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140542557,"clinical_significance":[],"seq_region_name":"7","id":"rs980036557"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796706821","alleles":["T","C"],"end":140542558,"feature_type":"variation","strand":1,"source":"dbSNP","start":140542558,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140542558,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140542566,"alleles":["TCTCTCTCT","TCTCT","TCTCTCT","TCTCTCTCTCT"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1563127624","clinical_significance":[]},{"end":140542561,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140542561,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs533306616","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140542562,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542562,"clinical_significance":[],"id":"rs1585587074","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1796707273","clinical_significance":[],"start":140542562,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140542567,"alleles":["TCTCTT","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1796707362","clinical_significance":[],"start":140542563,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140542565,"alleles":["CTC","-"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542564,"source":"dbSNP","strand":1,"feature_type":"variation","end":140542564,"alleles":["T","A"],"seq_region_name":"7","id":"rs1408511019","clinical_significance":[]},{"id":"rs1796707575","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542564,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","TT"],"end":140542564},{"clinical_significance":[],"id":"rs1423778794","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542564,"feature_type":"variation","strand":1,"end":140542567,"alleles":["TCTT","T"]},{"source":"dbSNP","start":140542564,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140542570,"alleles":["TCTTTTT","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796707778"},{"id":"rs1363253431","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140542565,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542565,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1796707973","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","-"],"end":140542565,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542565},{"id":"rs1796708077","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140542566,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542566,"source":"dbSNP"},{"source":"dbSNP","start":140542566,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTT","TTTTTTTTTTT","TTTTTTTTTTTT","TTTTTTTTTTTTT","TTTTTTTTTTTTTT","TTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT"],"end":140542587,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs771623397"},{"clinical_significance":[],"id":"rs1491158596","seq_region_name":"7","feature_type":"variation","strand":1,"end":140542566,"alleles":["-","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542567},{"end":140542567,"alleles":["T","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140542567,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs200792435"},{"seq_region_name":"7","id":"rs1404327138","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542568,"source":"dbSNP","strand":1,"feature_type":"variation","end":140542568,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1796709393","clinical_significance":[],"alleles":["T","C"],"end":140542569,"strand":1,"feature_type":"variation","start":140542569,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796709489","alleles":["TT","TTCTT"],"end":140542570,"feature_type":"variation","strand":1,"source":"dbSNP","start":140542569,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140542570,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140542570,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1463469724"},{"seq_region_name":"7","id":"rs1208068082","clinical_significance":[],"start":140542571,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140542571,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1796709832","clinical_significance":[],"start":140542572,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140542572,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140542573,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542573,"source":"dbSNP","seq_region_name":"7","id":"rs1246737001","clinical_significance":[]},{"seq_region_name":"7","id":"rs1399139709","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542574,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140542574},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796710148","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542575,"feature_type":"variation","strand":1,"end":140542574,"alleles":["-","C"]},{"feature_type":"variation","strand":1,"end":140542576,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542576,"clinical_significance":[],"seq_region_name":"7","id":"rs1796710248"},{"feature_type":"variation","strand":1,"end":140542577,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542577,"clinical_significance":[],"id":"rs1478734689","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140542578,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542578,"source":"dbSNP","seq_region_name":"7","id":"rs1796710453","clinical_significance":[]},{"clinical_significance":[],"id":"rs796948787","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["TT","C"],"end":140542579,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542578},{"clinical_significance":[],"seq_region_name":"7","id":"rs1189034190","feature_type":"variation","strand":1,"end":140542579,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542579},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796710732","end":140542583,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140542583,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1424026070","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542583,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TTTTTG","-"],"end":140542588},{"strand":1,"feature_type":"variation","alleles":["TTG","-"],"end":140542588,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542586,"source":"dbSNP","seq_region_name":"7","id":"rs1796711004","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542587,"feature_type":"variation","strand":1,"end":140542588,"alleles":["TG","-"],"clinical_significance":[],"id":"rs1481452278","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1427370713","source":"dbSNP","start":140542588,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","-"],"end":140542588,"feature_type":"variation","strand":1},{"start":140542588,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140542588,"strand":1,"feature_type":"variation","id":"rs1472748189","seq_region_name":"7","clinical_significance":[]},{"start":140542588,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["GAG","G"],"end":140542590,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585587257","clinical_significance":[]},{"clinical_significance":[],"id":"rs1796711748","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["GAG","-"],"end":140542590,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542588},{"clinical_significance":[],"seq_region_name":"7","id":"rs1160338263","feature_type":"variation","strand":1,"end":140542589,"alleles":["A","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542589},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796712118","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542589,"feature_type":"variation","strand":1,"end":140542589,"alleles":["A","-"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585587274","feature_type":"variation","strand":1,"alleles":["-","TTT"],"end":140542589,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542590},{"end":140542590,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140542590,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1274728110"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796712560","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542591,"feature_type":"variation","strand":1,"alleles":["TTT","TTTT","TTTTTTTTTTTTTT"],"end":140542593},{"clinical_significance":[],"id":"rs1414702631","seq_region_name":"7","source":"dbSNP","start":140542594,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140542594,"alleles":["C","A","T"],"feature_type":"variation","strand":1},{"end":140542596,"alleles":["CAC","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140542594,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796712983"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796713134","source":"dbSNP","start":140542594,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140542596,"alleles":["CAC","-"],"feature_type":"variation","strand":1},{"start":140542595,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C","T"],"end":140542595,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1476054178","clinical_significance":[]},{"end":140542596,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140542596,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796713496","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542597,"feature_type":"variation","strand":1,"end":140542597,"alleles":["T","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1796713680"},{"id":"rs1796713830","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140542597,"alleles":["T","TTTTTTT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542597,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1456073446","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140542598,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542598,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1796714185","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542599,"source":"dbSNP","strand":1,"feature_type":"variation","end":140542599,"alleles":["T","C"]},{"end":140542601,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140542601,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs986233138","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585587334","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140542604,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542604},{"seq_region_name":"7","id":"rs1796714657","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140542605,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542605,"source":"dbSNP"},{"id":"rs1042565393","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542607,"source":"dbSNP","strand":1,"feature_type":"variation","end":140542607,"alleles":["C","G"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542608,"source":"dbSNP","strand":1,"feature_type":"variation","end":140542608,"alleles":["A","C"],"seq_region_name":"7","id":"rs1585587341","clinical_significance":[]},{"start":140542610,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140542619,"alleles":["GCTGGAGTGC","GC"],"strand":1,"feature_type":"variation","id":"rs1796714954","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585587349","alleles":["A","G"],"end":140542615,"feature_type":"variation","strand":1,"source":"dbSNP","start":140542615,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140542617,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140542617,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585587358"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542618,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140542618,"seq_region_name":"7","id":"rs902705192","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140542619,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542619,"clinical_significance":[],"seq_region_name":"7","id":"rs1796715339"},{"seq_region_name":"7","id":"rs1350483249","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542620,"source":"dbSNP","strand":1,"feature_type":"variation","end":140542620,"alleles":["A","C"]},{"strand":1,"feature_type":"variation","end":140542621,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542621,"source":"dbSNP","seq_region_name":"7","id":"rs1796715551","clinical_significance":[]},{"id":"rs375329475","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140542625,"strand":1,"feature_type":"variation","start":140542625,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140542626,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542626,"source":"dbSNP","id":"rs113635938","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1463376628","feature_type":"variation","strand":1,"end":140542627,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542627},{"alleles":["A","G"],"end":140542628,"feature_type":"variation","strand":1,"source":"dbSNP","start":140542628,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs6962849"},{"seq_region_name":"7","id":"rs1260749707","clinical_significance":[],"start":140542630,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140542630,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"start":140542634,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C","G"],"end":140542634,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585587440","clinical_significance":[]},{"seq_region_name":"7","id":"rs1222774114","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542638,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140542638},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542644,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140542644,"id":"rs1585587459","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1362616487","clinical_significance":[],"start":140542646,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","G","T"],"end":140542646,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140542649,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542649,"clinical_significance":[],"seq_region_name":"7","id":"rs895367701"},{"clinical_significance":[],"id":"rs1229293439","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140542650,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542650},{"strand":1,"feature_type":"variation","end":140542653,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542653,"source":"dbSNP","id":"rs1796717003","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs549091232","clinical_significance":[],"end":140542656,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140542656,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1012360312","feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140542657,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542657},{"clinical_significance":[],"seq_region_name":"7","id":"rs1289942263","end":140542658,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140542658,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140542660,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140542660,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130515360","clinical_significance":[]},{"id":"rs1403975726","seq_region_name":"7","clinical_significance":[],"start":140542666,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140542666,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542667,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140542667,"clinical_significance":[],"seq_region_name":"7","id":"rs532080909"},{"seq_region_name":"7","id":"rs1227654251","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542668,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140542668},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542676,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140542676,"id":"rs1796717760","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140542685,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542685,"clinical_significance":[],"seq_region_name":"7","id":"rs1290519448"},{"alleles":["C","T"],"end":140542686,"feature_type":"variation","strand":1,"source":"dbSNP","start":140542686,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1453323364"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542689,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140542689,"id":"rs905642082","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796718183","feature_type":"variation","strand":1,"end":140542691,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542691},{"start":140542691,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TAGCT","TAGCTAGCT"],"end":140542695,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130515446","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542692,"feature_type":"variation","strand":1,"end":140542692,"alleles":["A","G","T"],"clinical_significance":[],"id":"rs951798809","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542696,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140542696,"clinical_significance":[],"seq_region_name":"7","id":"rs983212999"},{"source":"dbSNP","start":140542699,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140542699,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs774696896"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140542703,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542703,"source":"dbSNP","id":"rs1796718588","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs749693249","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140542704,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542704,"source":"dbSNP"},{"seq_region_name":"7","id":"rs768853672","clinical_significance":[],"end":140542705,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140542705,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140542706,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140542706,"alleles":["G","C"],"strand":1,"feature_type":"variation","id":"rs1796718881","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1244201970","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542707,"source":"dbSNP","strand":1,"feature_type":"variation","end":140542707,"alleles":["C","A","T"]},{"source":"dbSNP","start":140542708,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140542708,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs534709212"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1462395634","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542709,"feature_type":"variation","strand":1,"end":140542709,"alleles":["T","C"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542711,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140542711,"clinical_significance":[],"seq_region_name":"7","id":"rs1240687342"},{"source":"dbSNP","start":140542713,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140542713,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs186880171"},{"clinical_significance":[],"seq_region_name":"7","id":"rs571540119","source":"dbSNP","start":140542714,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140542714,"alleles":["C","T"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542716,"source":"dbSNP","strand":1,"feature_type":"variation","end":140542716,"alleles":["C","T"],"seq_region_name":"7","id":"rs1796719638","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130515576","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542717,"feature_type":"variation","strand":1,"end":140542717,"alleles":["C","T"]},{"strand":1,"feature_type":"variation","alleles":["A","AA"],"end":140542718,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542718,"source":"dbSNP","seq_region_name":"7","id":"rs35992797","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796719797","end":140542718,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140542718,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542719,"source":"dbSNP","strand":1,"feature_type":"variation","end":140542719,"alleles":["C","A","G","T"],"seq_region_name":"7","id":"rs975906260","clinical_significance":[]},{"clinical_significance":[],"id":"rs1315531310","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542720,"feature_type":"variation","strand":1,"end":140542720,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796720460","end":140542723,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140542723,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140542725,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542725,"clinical_significance":[],"id":"rs921876260","seq_region_name":"7"},{"source":"dbSNP","start":140542727,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140542727,"alleles":["T","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1380894140"},{"id":"rs1796720763","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140542727,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542727,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1471822245","seq_region_name":"7","feature_type":"variation","strand":1,"end":140542728,"alleles":["A","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542728},{"feature_type":"variation","strand":1,"end":140542733,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542733,"clinical_significance":[],"seq_region_name":"7","id":"rs1796723041"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542736,"source":"dbSNP","strand":1,"feature_type":"variation","end":140542736,"alleles":["T","C"],"id":"rs1443034042","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796723326","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140542739,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542739,"source":"dbSNP"},{"alleles":["A","G"],"end":140542746,"strand":1,"feature_type":"variation","start":140542746,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs539351084","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140542747,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542747,"source":"dbSNP","seq_region_name":"7","id":"rs1168947469","clinical_significance":[]},{"alleles":["G","A"],"end":140542750,"strand":1,"feature_type":"variation","start":140542750,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796723534","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140542752,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542752,"source":"dbSNP","seq_region_name":"7","id":"rs953317623","clinical_significance":[]},{"id":"rs376386629","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542754,"source":"dbSNP","strand":1,"feature_type":"variation","end":140542754,"alleles":["C","G","T"]},{"seq_region_name":"7","id":"rs1563127798","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542755,"source":"dbSNP","strand":1,"feature_type":"variation","end":140542755,"alleles":["G","A"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542756,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140542756,"clinical_significance":[],"seq_region_name":"7","id":"rs1796724140"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796724290","source":"dbSNP","start":140542758,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140542758,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542763,"feature_type":"variation","strand":1,"end":140542763,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1796724432"},{"alleles":["A","G"],"end":140542766,"feature_type":"variation","strand":1,"source":"dbSNP","start":140542766,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs369612993"},{"feature_type":"variation","strand":1,"end":140542767,"alleles":["T","C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542767,"clinical_significance":[],"seq_region_name":"7","id":"rs915226811"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140542781,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542781,"source":"dbSNP","id":"rs901745099","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs946692957","clinical_significance":[],"start":140542783,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140542783,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs367966248","alleles":["CTTCT","CT"],"end":140542793,"feature_type":"variation","strand":1,"source":"dbSNP","start":140542789,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542791,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140542791,"seq_region_name":"7","id":"rs1796725249","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796725362","alleles":["C","T"],"end":140542799,"feature_type":"variation","strand":1,"source":"dbSNP","start":140542799,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542805,"source":"dbSNP","strand":1,"feature_type":"variation","end":140542805,"alleles":["A","G"],"seq_region_name":"7","id":"rs1349409820","clinical_significance":[]},{"end":140542808,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140542808,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1410617776"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585587886","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542809,"feature_type":"variation","strand":1,"end":140542809,"alleles":["A","C"]},{"alleles":["C","A"],"end":140542811,"feature_type":"variation","strand":1,"source":"dbSNP","start":140542811,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796725738"},{"seq_region_name":"7","id":"rs1383019135","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542812,"source":"dbSNP","strand":1,"feature_type":"variation","end":140542812,"alleles":["T","C"]},{"clinical_significance":[],"id":"rs1796725945","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140542813,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542813},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542814,"feature_type":"variation","strand":1,"end":140542814,"alleles":["C","T"],"clinical_significance":[],"id":"rs2130515874","seq_region_name":"7"},{"seq_region_name":"7","id":"rs148724516","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542817,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140542817},{"seq_region_name":"7","id":"rs1248432386","clinical_significance":[],"end":140542818,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140542818,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1796726434","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140542820,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542820,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1796726594","seq_region_name":"7","feature_type":"variation","strand":1,"end":140542822,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542822},{"end":140542825,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140542825,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796726720"},{"start":140542826,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140542826,"alleles":["A","C"],"strand":1,"feature_type":"variation","id":"rs1796726858","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs536806934","clinical_significance":[],"start":140542828,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140542828,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs555510493","clinical_significance":[],"alleles":["G","T"],"end":140542831,"strand":1,"feature_type":"variation","start":140542831,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542834,"feature_type":"variation","strand":1,"end":140542834,"alleles":["G","A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs923989607"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542843,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140542843,"clinical_significance":[],"seq_region_name":"7","id":"rs1408990398"},{"start":140542844,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140542844,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796728036","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542845,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140542845,"clinical_significance":[],"seq_region_name":"7","id":"rs1796728169"},{"source":"dbSNP","start":140542846,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140542846,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796728328"},{"clinical_significance":[],"seq_region_name":"7","id":"rs953485578","source":"dbSNP","start":140542847,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140542847,"alleles":["T","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1247901862","feature_type":"variation","strand":1,"end":140542848,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542848},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542850,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140542850,"seq_region_name":"7","id":"rs1796728828","clinical_significance":[]},{"end":140542851,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140542851,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs767671410"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542853,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140542853,"seq_region_name":"7","id":"rs1585587994","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796729171","clinical_significance":[],"start":140542854,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140542855,"alleles":["CC","C"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542855,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140542855,"id":"rs573733648","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs191965771","end":140542856,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140542856,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1296572786","end":140542857,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140542857,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs895428068","source":"dbSNP","start":140542858,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140542858,"alleles":["G","A","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs7800558","clinical_significance":[],"end":140542861,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140542861,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140542862,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542862,"clinical_significance":[],"seq_region_name":"7","id":"rs949605889"},{"alleles":["C","T"],"end":140542868,"feature_type":"variation","strand":1,"source":"dbSNP","start":140542868,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs981130040"},{"end":140542871,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140542871,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs926945312","seq_region_name":"7","clinical_significance":[]},{"start":140542873,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140542873,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796730169","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796730252","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140542874,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542874,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542877,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140542877,"seq_region_name":"7","id":"rs1163599226","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140542878,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542878,"source":"dbSNP","seq_region_name":"7","id":"rs1796730456","clinical_significance":[]},{"start":140542884,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140542884,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796730542","clinical_significance":[]},{"seq_region_name":"7","id":"rs937119868","clinical_significance":[],"strand":1,"feature_type":"variation","end":140542885,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542885,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs577551831","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542887,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140542887},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542888,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140542888,"clinical_significance":[],"seq_region_name":"7","id":"rs545317957"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796730990","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542890,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140542890},{"feature_type":"variation","strand":1,"end":140542894,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542894,"clinical_significance":[],"seq_region_name":"7","id":"rs1796731078"},{"seq_region_name":"7","id":"rs1206784922","clinical_significance":[],"alleles":["A","G"],"end":140542900,"strand":1,"feature_type":"variation","start":140542900,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1796731294","clinical_significance":[],"alleles":["C","T"],"end":140542902,"strand":1,"feature_type":"variation","start":140542902,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140542904,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140542904,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1796731414","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1711674509","source":"dbSNP","start":140542908,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140542908,"alleles":["C","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1249169456","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542910,"source":"dbSNP","strand":1,"feature_type":"variation","end":140542910,"alleles":["A","G"]},{"end":140542911,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140542911,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs374347931","clinical_significance":[]},{"id":"rs1269533743","seq_region_name":"7","clinical_significance":[],"end":140542915,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140542915,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140542916,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542916,"source":"dbSNP","id":"rs1796731708","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs887460146","source":"dbSNP","start":140542917,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140542917,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1796731894","clinical_significance":[],"alleles":["G","A"],"end":140542922,"strand":1,"feature_type":"variation","start":140542922,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130516311","source":"dbSNP","start":140542923,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140542923,"alleles":["A","T"],"feature_type":"variation","strand":1},{"alleles":["TTTT","TTT"],"end":140542934,"strand":1,"feature_type":"variation","start":140542931,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs940551225","clinical_significance":[]},{"end":140542932,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140542932,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1036125622"},{"seq_region_name":"7","id":"rs530636038","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542942,"source":"dbSNP","strand":1,"feature_type":"variation","end":140542942,"alleles":["A","C","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796732384","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542943,"feature_type":"variation","strand":1,"end":140542943,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1014689005","source":"dbSNP","start":140542946,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140542946,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542950,"feature_type":"variation","strand":1,"end":140542950,"alleles":["A","G"],"clinical_significance":[],"id":"rs1585588254","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs965813584","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542952,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140542952},{"seq_region_name":"7","id":"rs1304882814","clinical_significance":[],"alleles":["G","A","C"],"end":140542957,"strand":1,"feature_type":"variation","start":140542957,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs997797555","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542962,"feature_type":"variation","strand":1,"end":140542962,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1796733078","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140542963,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542963,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1028804983","source":"dbSNP","start":140542967,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140542967,"alleles":["T","G"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140542971,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542971,"clinical_significance":[],"id":"rs1796733296","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130516433","alleles":["A","C"],"end":140542978,"feature_type":"variation","strand":1,"source":"dbSNP","start":140542978,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585588311","feature_type":"variation","strand":1,"end":140542979,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140542979},{"seq_region_name":"7","id":"rs1285747361","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140542980,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542980,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs761687782","end":140542982,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140542982,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["C","CC"],"end":140542982,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542982,"source":"dbSNP","seq_region_name":"7","id":"rs1403685328","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542983,"source":"dbSNP","strand":1,"feature_type":"variation","end":140542983,"alleles":["G","A"],"seq_region_name":"7","id":"rs997369176","clinical_significance":[]},{"seq_region_name":"7","id":"rs1028989143","clinical_significance":[],"strand":1,"feature_type":"variation","end":140542996,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140542996,"source":"dbSNP"},{"source":"dbSNP","start":140543001,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140543001,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1796733993","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1796734140","clinical_significance":[],"end":140543002,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140543002,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs889131586","source":"dbSNP","start":140543003,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140543003,"feature_type":"variation","strand":1},{"end":140543004,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140543004,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796734440"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543007,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140543007,"seq_region_name":"7","id":"rs1796734603","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1001235359","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140543008,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543008},{"seq_region_name":"7","id":"rs1796734941","clinical_significance":[],"strand":1,"feature_type":"variation","end":140543010,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543010,"source":"dbSNP"},{"source":"dbSNP","start":140543011,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140543011,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1032446423"},{"seq_region_name":"7","id":"rs990099046","clinical_significance":[],"strand":1,"feature_type":"variation","end":140543012,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543012,"source":"dbSNP"},{"seq_region_name":"7","id":"rs748600495","clinical_significance":[],"alleles":["C","CC"],"end":140543014,"strand":1,"feature_type":"variation","start":140543014,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs914468614","source":"dbSNP","start":140543022,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140543022,"alleles":["C","T"],"feature_type":"variation","strand":1},{"alleles":["CTC","C"],"end":140543024,"strand":1,"feature_type":"variation","start":140543022,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1796735734","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1201462007","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543025,"feature_type":"variation","strand":1,"end":140543025,"alleles":["A","C"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543026,"feature_type":"variation","strand":1,"end":140543044,"alleles":["CTGCCTCTACCTGCCTCTA","CTGCCTCTA"],"clinical_significance":[],"seq_region_name":"7","id":"rs1796736043"},{"seq_region_name":"7","id":"rs1796736205","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543028,"source":"dbSNP","strand":1,"feature_type":"variation","end":140543028,"alleles":["G","T"]},{"id":"rs2130516638","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140543033,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543033,"source":"dbSNP"},{"source":"dbSNP","start":140543034,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140543034,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585588451"},{"feature_type":"variation","strand":1,"end":140543038,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543038,"clinical_significance":[],"seq_region_name":"7","id":"rs1368938304"},{"clinical_significance":[],"seq_region_name":"7","id":"rs550842060","source":"dbSNP","start":140543040,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140543040,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543041,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140543041,"clinical_significance":[],"id":"rs1796736847","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1796736998","clinical_significance":[],"start":140543043,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140543043,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs978031124","source":"dbSNP","start":140543046,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140543046,"alleles":["T","G"],"feature_type":"variation","strand":1},{"id":"rs1796737226","seq_region_name":"7","clinical_significance":[],"end":140543049,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140543049,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1334533555","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543050,"source":"dbSNP","strand":1,"feature_type":"variation","end":140543050,"alleles":["G","A"]},{"id":"rs1796737467","seq_region_name":"7","clinical_significance":[],"end":140543051,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140543051,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs2130516730","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543057,"source":"dbSNP","strand":1,"feature_type":"variation","end":140543057,"alleles":["A","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543058,"feature_type":"variation","strand":1,"end":140543058,"alleles":["G","GG"],"clinical_significance":[],"seq_region_name":"7","id":"rs61588730"},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140543058,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543058,"source":"dbSNP","seq_region_name":"7","id":"rs1796737564","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543061,"feature_type":"variation","strand":1,"end":140543061,"alleles":["T","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1796737877"},{"clinical_significance":[],"seq_region_name":"7","id":"rs924063114","source":"dbSNP","start":140543062,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140543062,"feature_type":"variation","strand":1},{"alleles":["G","A"],"end":140543063,"strand":1,"feature_type":"variation","start":140543063,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796738212","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140543065,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543065,"clinical_significance":[],"seq_region_name":"7","id":"rs1283538639"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543074,"feature_type":"variation","strand":1,"end":140543074,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1486939400"},{"clinical_significance":[],"id":"rs939450503","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543075,"feature_type":"variation","strand":1,"end":140543075,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1259172763","alleles":["CCCC","CCC"],"end":140543083,"feature_type":"variation","strand":1,"source":"dbSNP","start":140543080,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140543081,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543081,"source":"dbSNP","id":"rs1365197996","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs560742991","alleles":["C","T"],"end":140543083,"feature_type":"variation","strand":1,"source":"dbSNP","start":140543083,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1229964579","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140543084,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543084},{"seq_region_name":"7","id":"rs1057058170","clinical_significance":[],"alleles":["C","G"],"end":140543085,"strand":1,"feature_type":"variation","start":140543085,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796739236","feature_type":"variation","strand":1,"end":140543096,"alleles":["ACTGAGAC","ACTGAGACTGAGAC"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543089},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796739363","alleles":["A","T"],"end":140543097,"feature_type":"variation","strand":1,"source":"dbSNP","start":140543097,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140543101,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["-","A"],"end":140543100,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796739474"},{"strand":1,"feature_type":"variation","end":140543102,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543102,"source":"dbSNP","seq_region_name":"7","id":"rs1796739572","clinical_significance":[]},{"start":140543103,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140543103,"strand":1,"feature_type":"variation","id":"rs1796739684","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","A"],"end":140543104,"feature_type":"variation","strand":1,"source":"dbSNP","start":140543104,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1796739784","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796739892","source":"dbSNP","start":140543105,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140543105,"alleles":["G","C"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543106,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TTTTT","TTTT"],"end":140543110,"seq_region_name":"7","id":"rs1796740001","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1180046309","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543107,"feature_type":"variation","strand":1,"alleles":["TTTTCTTTTCTTTTCTTTT","TTTTCTTTT","TTTTCTTTTCTTTT","TTTTCTTTTCTTTTCTTTTCTTTT"],"end":140543125},{"alleles":["T","C"],"end":140543110,"feature_type":"variation","strand":1,"source":"dbSNP","start":140543110,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796740282"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585588591","end":140543111,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140543111,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140543112,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543112,"clinical_significance":[],"seq_region_name":"7","id":"rs1796740460"},{"strand":1,"feature_type":"variation","end":140543116,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543116,"source":"dbSNP","seq_region_name":"7","id":"rs1265137068","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796740681","alleles":["TTTT","TTT"],"end":140543120,"feature_type":"variation","strand":1,"source":"dbSNP","start":140543117,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1271931716","clinical_significance":[],"strand":1,"feature_type":"variation","end":140543131,"alleles":["TTTTCTTTTTTTTTT","TTTT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543117,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1331069105","seq_region_name":"7","source":"dbSNP","start":140543118,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140543124,"alleles":["TTTCTTT","TTT"],"feature_type":"variation","strand":1},{"end":140543121,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140543121,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs201765926"},{"alleles":["T","C","G"],"end":140543122,"strand":1,"feature_type":"variation","start":140543122,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1177994552","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1563128068","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543122,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TTTT","TTTTCTTTTT"],"end":140543125},{"source":"dbSNP","start":140543122,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140543137,"alleles":["TTTTTTTTTTTTTTTT","TTTTTTTTTT","TTTTTTTTTTTT","TTTTTTTTTTTTT","TTTTTTTTTTTTTT","TTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTT"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs35896324"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1468129202","feature_type":"variation","strand":1,"end":140543125,"alleles":["TTT","TTTCTTT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543123},{"clinical_significance":[],"seq_region_name":"7","id":"rs1340992146","end":140543125,"alleles":["TT","TTCTT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140543124,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140543125,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140543125,"alleles":["T","TCT"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs201561818"},{"seq_region_name":"7","id":"rs1563128075","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543125,"source":"dbSNP","strand":1,"feature_type":"variation","end":140543125,"alleles":["T","C","G"]},{"end":140543125,"alleles":["-","C"],"strand":1,"feature_type":"variation","start":140543126,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs199931684","clinical_significance":[]},{"end":140543126,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140543126,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs10952733","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs370088507","source":"dbSNP","start":140543126,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TT","C"],"end":140543127,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543127,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140543127,"seq_region_name":"7","id":"rs34608876","clinical_significance":[]},{"seq_region_name":"7","id":"rs1554463306","clinical_significance":[],"end":140543128,"alleles":["TT","C"],"strand":1,"feature_type":"variation","start":140543127,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["T","C"],"end":140543128,"strand":1,"feature_type":"variation","start":140543128,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1444507699","clinical_significance":[]},{"seq_region_name":"7","id":"rs1563128098","clinical_significance":[],"alleles":["TT","TTCTT"],"end":140543129,"strand":1,"feature_type":"variation","start":140543128,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140543129,"alleles":["T","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543129,"clinical_significance":[],"seq_region_name":"7","id":"rs1796743084"},{"start":140543131,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140543131,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","id":"rs1796743232","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1025130833","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140543132,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543132},{"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140543137,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543137,"source":"dbSNP","seq_region_name":"7","id":"rs1796743489","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543138,"source":"dbSNP","strand":1,"feature_type":"variation","end":140543138,"alleles":["G","T"],"id":"rs1450701992","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140543138,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140543138,"alleles":["G","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796743706"},{"end":140543140,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140543140,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1796743824","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140543141,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543141,"source":"dbSNP","id":"rs1190575524","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130517196","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140543142,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543142},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140543143,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543143,"clinical_significance":[],"seq_region_name":"7","id":"rs1796744160"},{"seq_region_name":"7","id":"rs1201859607","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543146,"source":"dbSNP","strand":1,"feature_type":"variation","end":140543146,"alleles":["G","T"]},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140543148,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543148,"source":"dbSNP","id":"rs1344850300","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543150,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140543150,"clinical_significance":[],"seq_region_name":"7","id":"rs1796744641"},{"clinical_significance":[],"seq_region_name":"7","id":"rs571640416","alleles":["C","T"],"end":140543154,"feature_type":"variation","strand":1,"source":"dbSNP","start":140543154,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543156,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140543156,"clinical_significance":[],"seq_region_name":"7","id":"rs538628085"},{"seq_region_name":"7","id":"rs1252389485","clinical_significance":[],"start":140543159,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140543159,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"id":"rs1796745332","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543163,"source":"dbSNP","strand":1,"feature_type":"variation","end":140543163,"alleles":["A","G"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543166,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140543166,"id":"rs1585588934","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","A"],"end":140543167,"strand":1,"feature_type":"variation","start":140543167,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs971009420","clinical_significance":[]},{"alleles":["A","G"],"end":140543169,"strand":1,"feature_type":"variation","start":140543169,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585588951","clinical_significance":[]},{"end":140543172,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140543172,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796746025"},{"clinical_significance":[],"seq_region_name":"7","id":"rs981010705","end":140543177,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140543177,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs2130517306","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543182,"source":"dbSNP","strand":1,"feature_type":"variation","end":140543182,"alleles":["G","C"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543186,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140543186,"seq_region_name":"7","id":"rs1297388467","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543193,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140543193,"seq_region_name":"7","id":"rs1585588989","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543195,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140543195,"id":"rs551272266","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","A"],"end":140543196,"strand":1,"feature_type":"variation","start":140543196,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1383111747","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796747167","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543200,"source":"dbSNP","strand":1,"feature_type":"variation","end":140543200,"alleles":["C","A"]},{"id":"rs1796747287","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140543201,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543201,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543207,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140543207,"id":"rs1796747416","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1412546067","alleles":["T","C"],"end":140543208,"feature_type":"variation","strand":1,"source":"dbSNP","start":140543208,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543209,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140543209,"clinical_significance":[],"seq_region_name":"7","id":"rs1796747628"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543214,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GCTCAAGTGATCTTCCTACCTCAGCT","GCT"],"end":140543239,"id":"rs1796747727","seq_region_name":"7","clinical_significance":[]},{"start":140543215,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140543215,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1393780405","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543230,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140543230,"seq_region_name":"7","id":"rs1796747938","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585589052","clinical_significance":[],"start":140543231,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140543231,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140543231,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AC","ACAC"],"end":140543232,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796748147"},{"clinical_significance":[],"id":"rs1335913969","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543232,"feature_type":"variation","strand":1,"end":140543232,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585589075","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543236,"feature_type":"variation","strand":1,"end":140543236,"alleles":["A","C"]},{"source":"dbSNP","start":140543237,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140543237,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs771775794"},{"clinical_significance":[],"id":"rs1400953024","seq_region_name":"7","alleles":["C","T"],"end":140543238,"feature_type":"variation","strand":1,"source":"dbSNP","start":140543238,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543241,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140543241,"seq_region_name":"7","id":"rs1796748641","clinical_significance":[]},{"clinical_significance":[],"id":"rs1585589095","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543245,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140543245},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543247,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140543247,"seq_region_name":"7","id":"rs1585589103","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585589111","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543248,"source":"dbSNP","strand":1,"feature_type":"variation","end":140543248,"alleles":["A","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543249,"source":"dbSNP","strand":1,"feature_type":"variation","end":140543249,"alleles":["G","T"],"id":"rs1298649727","seq_region_name":"7","clinical_significance":[]},{"start":140543250,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140543250,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs937022493","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs984838727","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543251,"feature_type":"variation","strand":1,"end":140543251,"alleles":["A","G"]},{"end":140543252,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140543252,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1167766272","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1445397916","clinical_significance":[],"strand":1,"feature_type":"variation","end":140543253,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543253,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs569530321","feature_type":"variation","strand":1,"end":140543254,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543254},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796749767","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140543256,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543256},{"seq_region_name":"7","id":"rs1563128172","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140543257,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543257,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543265,"source":"dbSNP","strand":1,"feature_type":"variation","end":140543265,"alleles":["C","T"],"seq_region_name":"7","id":"rs948195854","clinical_significance":[]},{"alleles":["G","A","C"],"end":140543266,"strand":1,"feature_type":"variation","start":140543266,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs908975194","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543267,"source":"dbSNP","strand":1,"feature_type":"variation","end":140543267,"alleles":["A","G"],"seq_region_name":"7","id":"rs1441909576","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796750241","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140543268,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543268},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796750350","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543270,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140543270},{"seq_region_name":"7","id":"rs1585589200","clinical_significance":[],"end":140543271,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","start":140543271,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs940422618","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543272,"source":"dbSNP","strand":1,"feature_type":"variation","end":140543272,"alleles":["C","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543273,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140543273,"id":"rs1198050269","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585589228","source":"dbSNP","start":140543276,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140543276,"alleles":["A","C","T"],"feature_type":"variation","strand":1},{"start":140543277,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140543277,"strand":1,"feature_type":"variation","id":"rs1796751082","seq_region_name":"7","clinical_significance":[]},{"id":"rs1796751259","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140543278,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543278,"source":"dbSNP"},{"alleles":["-","CTT","T"],"end":140543284,"feature_type":"variation","strand":1,"source":"dbSNP","start":140543285,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796751424"},{"start":140543285,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140543285,"alleles":["A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1430305928","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796751803","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140543286,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543286,"source":"dbSNP"},{"seq_region_name":"7","id":"rs36113743","clinical_significance":[],"start":140543286,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTT","TTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT"],"end":140543305,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1328978196","feature_type":"variation","strand":1,"alleles":["-","A"],"end":140543289,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543290},{"end":140543292,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140543292,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1393029650","clinical_significance":[]},{"id":"rs1796752922","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["-","A"],"end":140543298,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543299,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543301,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140543301,"id":"rs1368638219","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543305,"source":"dbSNP","strand":1,"feature_type":"variation","end":140543305,"alleles":["T","C"],"seq_region_name":"7","id":"rs1397011550","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796753345","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543305,"source":"dbSNP","strand":1,"feature_type":"variation","end":140543306,"alleles":["TA","-"]},{"alleles":["-","TA"],"end":140543305,"feature_type":"variation","strand":1,"source":"dbSNP","start":140543306,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1796753491","seq_region_name":"7"},{"seq_region_name":"7","id":"rs58476423","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","AA"],"end":140543306,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543306,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543306,"feature_type":"variation","strand":1,"end":140543306,"alleles":["A","C","T"],"clinical_significance":[],"id":"rs945320790","seq_region_name":"7"},{"source":"dbSNP","start":140543306,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","-"],"end":140543306,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1425045487"},{"start":140543306,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140543307,"alleles":["AC","-"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796754088","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796754237","feature_type":"variation","strand":1,"alleles":["ACG","-"],"end":140543308,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543306},{"clinical_significance":[],"seq_region_name":"7","id":"rs1325378187","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543307,"feature_type":"variation","strand":1,"end":140543307,"alleles":["C","A","T"]},{"feature_type":"variation","strand":1,"end":140543307,"alleles":["-","TTTTTTTTTTTTTTTTTTTTT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543308,"clinical_significance":[],"seq_region_name":"7","id":"rs1796754591"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1472617853","end":140543308,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140543308,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["TTTTTT","TTTTTTT"],"end":140543314,"strand":1,"feature_type":"variation","start":140543309,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1036175159","clinical_significance":[]},{"source":"dbSNP","start":140543315,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140543315,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs923105095"},{"start":140543317,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140543317,"alleles":["A","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs933122762","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543318,"source":"dbSNP","strand":1,"feature_type":"variation","end":140543318,"alleles":["G","T"],"seq_region_name":"7","id":"rs1796755514","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796755677","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543321,"feature_type":"variation","strand":1,"end":140543321,"alleles":["A","G"]},{"clinical_significance":[],"id":"rs1262969317","seq_region_name":"7","source":"dbSNP","start":140543323,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140543327,"alleles":["GGGGG","GGGGGG"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1465722676","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543325,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140543325},{"clinical_significance":[],"seq_region_name":"7","id":"rs1211162500","alleles":["G","A"],"end":140543326,"feature_type":"variation","strand":1,"source":"dbSNP","start":140543326,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130517874","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543333,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140543333},{"seq_region_name":"7","id":"rs1796756299","clinical_significance":[],"alleles":["G","A"],"end":140543335,"strand":1,"feature_type":"variation","start":140543335,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140543339,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140543339,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs1796756482","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1796756622","seq_region_name":"7","alleles":["CCC","CC"],"end":140543343,"feature_type":"variation","strand":1,"source":"dbSNP","start":140543341,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs867965397","seq_region_name":"7","end":140543342,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140543342,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140543343,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543343,"source":"dbSNP","id":"rs1796756915","seq_region_name":"7","clinical_significance":[]},{"id":"rs1796757068","seq_region_name":"7","clinical_significance":[],"start":140543347,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140543347,"strand":1,"feature_type":"variation"},{"alleles":["T","G"],"end":140543348,"feature_type":"variation","strand":1,"source":"dbSNP","start":140543348,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1490934603"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543351,"feature_type":"variation","strand":1,"end":140543351,"alleles":["T","C"],"clinical_significance":[],"id":"rs1796757390","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs889007793","source":"dbSNP","start":140543359,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140543359,"alleles":["T","G"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543361,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140543361,"seq_region_name":"7","id":"rs1796757700","clinical_significance":[]},{"id":"rs1207652025","seq_region_name":"7","clinical_significance":[],"end":140543364,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140543364,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543368,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140543368,"clinical_significance":[],"seq_region_name":"7","id":"rs1355251213"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543373,"source":"dbSNP","strand":1,"feature_type":"variation","end":140543373,"alleles":["A","G"],"seq_region_name":"7","id":"rs1000886596","clinical_significance":[]},{"end":140543383,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140543383,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs368450964","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1004583933","source":"dbSNP","start":140543384,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140543384,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1379581696","feature_type":"variation","strand":1,"end":140543389,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543389},{"alleles":["A","G","T"],"end":140543395,"strand":1,"feature_type":"variation","start":140543395,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1405522220","clinical_significance":[]},{"id":"rs1796759108","seq_region_name":"7","clinical_significance":[],"alleles":["A","G"],"end":140543397,"strand":1,"feature_type":"variation","start":140543397,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["G","A"],"end":140543400,"strand":1,"feature_type":"variation","start":140543400,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796759256","clinical_significance":[]},{"alleles":["C","A","T"],"end":140543401,"feature_type":"variation","strand":1,"source":"dbSNP","start":140543401,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs569205176"},{"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140543402,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543402,"source":"dbSNP","seq_region_name":"7","id":"rs1036025880","clinical_significance":[]},{"id":"rs1796759834","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140543403,"strand":1,"feature_type":"variation","start":140543403,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140543414,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140543414,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs183703223"},{"clinical_significance":[],"id":"rs534749874","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543415,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140543415},{"clinical_significance":[],"seq_region_name":"7","id":"rs1009653541","source":"dbSNP","start":140543418,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140543418,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1796760236","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543428,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140543428},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796760335","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543429,"feature_type":"variation","strand":1,"end":140543429,"alleles":["C","T"]},{"alleles":["G","A","C"],"end":140543431,"strand":1,"feature_type":"variation","start":140543431,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1318484702","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796760557","feature_type":"variation","strand":1,"end":140543444,"alleles":["TCTTTTCT","TCT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543437},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796760650","source":"dbSNP","start":140543439,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TTTT","TTTTT"],"end":140543442,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140543442,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543442,"clinical_significance":[],"id":"rs1383533168","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140543445,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543445,"clinical_significance":[],"id":"rs1025183172","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140543452,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543452,"source":"dbSNP","seq_region_name":"7","id":"rs772837018","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543455,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140543455,"seq_region_name":"7","id":"rs1796761054","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543457,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140543457,"id":"rs1585589656","seq_region_name":"7","clinical_significance":[]},{"id":"rs1796761266","seq_region_name":"7","clinical_significance":[],"start":140543459,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140543459,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140543460,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543460,"clinical_significance":[],"id":"rs1796761368","seq_region_name":"7"},{"end":140543463,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140543463,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1386841686"},{"clinical_significance":[],"seq_region_name":"7","id":"rs970891607","feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140543469,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543469},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543470,"feature_type":"variation","strand":1,"end":140543470,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1325020292"},{"clinical_significance":[],"seq_region_name":"7","id":"rs997259548","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140543471,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543471},{"id":"rs1029129001","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543473,"source":"dbSNP","strand":1,"feature_type":"variation","end":140543473,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1002332226","source":"dbSNP","start":140543474,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140543474,"alleles":["G","A"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140543478,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543478,"clinical_significance":[],"id":"rs1796762106","seq_region_name":"7"},{"alleles":["T","C"],"end":140543480,"strand":1,"feature_type":"variation","start":140543480,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1033951901","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140543483,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543483,"clinical_significance":[],"seq_region_name":"7","id":"rs1282999532"},{"seq_region_name":"7","id":"rs1796762401","clinical_significance":[],"end":140543491,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140543491,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1796762504","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543495,"source":"dbSNP","strand":1,"feature_type":"variation","end":140543497,"alleles":["AAA","AA"]},{"id":"rs552772076","seq_region_name":"7","clinical_significance":[],"start":140543501,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140543501,"alleles":["C","A","T"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543504,"source":"dbSNP","strand":1,"feature_type":"variation","end":140543504,"alleles":["C","A"],"id":"rs1330275133","seq_region_name":"7","clinical_significance":[]},{"start":140543506,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140543506,"strand":1,"feature_type":"variation","id":"rs1796762727","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543512,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GGG","GG"],"end":140543514,"id":"rs1796762823","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1272793946","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543519,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140543519},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140543520,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543520,"clinical_significance":[],"seq_region_name":"7","id":"rs187417831"},{"source":"dbSNP","start":140543523,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140543523,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130518390"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543525,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140543525,"clinical_significance":[],"seq_region_name":"7","id":"rs1796763050"},{"start":140543526,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140543526,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1011328529","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs750149812","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543534,"feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140543534},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543536,"source":"dbSNP","strand":1,"feature_type":"variation","end":140543536,"alleles":["A","C"],"seq_region_name":"7","id":"rs2130518428","clinical_significance":[]},{"end":140543542,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140543542,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1350666664"},{"seq_region_name":"7","id":"rs1796763487","clinical_significance":[],"start":140543545,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140543550,"alleles":["CCCCCC","CCCCC","CCCCCCC"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543546,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140543546,"clinical_significance":[],"seq_region_name":"7","id":"rs1796763641"},{"seq_region_name":"7","id":"rs1796763751","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543549,"source":"dbSNP","strand":1,"feature_type":"variation","end":140543549,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs984502205","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140543550,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543550},{"clinical_significance":[],"id":"rs1796763954","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543551,"feature_type":"variation","strand":1,"end":140543551,"alleles":["A","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1269621999","feature_type":"variation","strand":1,"end":140543559,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543559},{"clinical_significance":[],"seq_region_name":"7","id":"rs1471206738","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543560,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140543560},{"seq_region_name":"7","id":"rs908852044","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140543561,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543561,"source":"dbSNP"},{"start":140543562,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140543562,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs967261079","clinical_significance":[]},{"alleles":["C","T"],"end":140543567,"strand":1,"feature_type":"variation","start":140543567,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs142328457","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140543571,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543571,"clinical_significance":[],"seq_region_name":"7","id":"rs78127982"},{"strand":1,"feature_type":"variation","end":140543572,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543572,"source":"dbSNP","id":"rs1244231208","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585589871","clinical_significance":[],"start":140543576,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140543576,"strand":1,"feature_type":"variation"},{"start":140543577,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140543577,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs922985846","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140543578,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543578,"source":"dbSNP","seq_region_name":"7","id":"rs961104018","clinical_significance":[]},{"start":140543580,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140543581,"alleles":["CC","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1246832618","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130518579","clinical_significance":[],"end":140543581,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140543581,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796765253","source":"dbSNP","start":140543582,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140543582,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1203759598","alleles":["C","T"],"end":140543584,"feature_type":"variation","strand":1,"source":"dbSNP","start":140543584,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1796765471","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140543603,"alleles":["TTTATTTTATTTTATTTT","TTTATTTTATTTT","TTTATTTTATTTTATTTTATTTT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543586,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543589,"feature_type":"variation","strand":1,"end":140543589,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1796765614"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140543594,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543594,"source":"dbSNP","seq_region_name":"7","id":"rs111660869","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1473454120","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140543595,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543595},{"strand":1,"feature_type":"variation","end":140543599,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543599,"source":"dbSNP","seq_region_name":"7","id":"rs1796765956","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796766056","clinical_significance":[],"alleles":["A","-"],"end":140543599,"strand":1,"feature_type":"variation","start":140543599,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140543607,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140543607,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796766153"},{"source":"dbSNP","start":140543610,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140543610,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1218620144"},{"clinical_significance":[],"id":"rs1339807376","seq_region_name":"7","source":"dbSNP","start":140543612,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140543612,"alleles":["T","G"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140543615,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543615,"source":"dbSNP","id":"rs916612144","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543617,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140543617,"seq_region_name":"7","id":"rs1156769278","clinical_significance":[]},{"start":140543618,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140543618,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796766636","clinical_significance":[]},{"start":140543625,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140543625,"strand":1,"feature_type":"variation","id":"rs2130518727","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140543626,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543626,"source":"dbSNP","seq_region_name":"7","id":"rs1363145179","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796767130","clinical_significance":[],"strand":1,"feature_type":"variation","end":140543628,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543628,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs948253178","source":"dbSNP","start":140543629,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140543629,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140543632,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543632,"clinical_significance":[],"seq_region_name":"7","id":"rs1458391254"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796767462","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543633,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140543633},{"end":140543637,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140543637,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796767563"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543639,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140543639,"seq_region_name":"7","id":"rs2130518797","clinical_significance":[]},{"source":"dbSNP","start":140543640,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140543640,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130518809"},{"id":"rs910501099","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140543646,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543646,"source":"dbSNP"},{"source":"dbSNP","start":140543650,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140543650,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796767797"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1164466312","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543656,"feature_type":"variation","strand":1,"end":140543656,"alleles":["T","C"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543660,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140543660,"seq_region_name":"7","id":"rs1357570741","clinical_significance":[]},{"seq_region_name":"7","id":"rs532747378","clinical_significance":[],"start":140543662,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140543662,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543663,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140543663,"clinical_significance":[],"seq_region_name":"7","id":"rs560781156"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796771599","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543666,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140543666},{"clinical_significance":[],"id":"rs940902660","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543671,"feature_type":"variation","strand":1,"end":140543671,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130518901","feature_type":"variation","strand":1,"end":140543674,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543674},{"id":"rs533133049","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543675,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140543675},{"clinical_significance":[],"seq_region_name":"7","id":"rs528248431","feature_type":"variation","strand":1,"end":140543676,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543676},{"source":"dbSNP","start":140543679,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140543679,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1796772385","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585590088","feature_type":"variation","strand":1,"end":140543681,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543681},{"feature_type":"variation","strand":1,"end":140543686,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543686,"clinical_significance":[],"seq_region_name":"7","id":"rs1796772747"},{"seq_region_name":"7","id":"rs901520269","clinical_significance":[],"start":140543687,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140543687,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140543694,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543694,"source":"dbSNP","id":"rs1796773090","seq_region_name":"7","clinical_significance":[]},{"id":"rs1351413826","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543697,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140543697},{"seq_region_name":"7","id":"rs1796773440","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140543698,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543698,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1796773596","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140543701,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543701,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1585590137","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543702,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140543702},{"feature_type":"variation","strand":1,"end":140543703,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543703,"clinical_significance":[],"id":"rs1389183090","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1412056301","seq_region_name":"7","end":140543704,"alleles":["CC","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140543703,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1585590178","clinical_significance":[],"end":140543704,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140543704,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140543706,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140543706,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1183880458","seq_region_name":"7"},{"id":"rs1305381619","seq_region_name":"7","clinical_significance":[],"alleles":["-","TA"],"end":140543706,"strand":1,"feature_type":"variation","start":140543707,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796774858","alleles":["A","G"],"end":140543711,"feature_type":"variation","strand":1,"source":"dbSNP","start":140543711,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140543713,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140543713,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs932959947"},{"source":"dbSNP","start":140543714,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140543714,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs71543378"},{"source":"dbSNP","start":140543715,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140543715,"alleles":["T","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1483943798"},{"start":140543717,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C","G"],"end":140543717,"strand":1,"feature_type":"variation","id":"rs1235294600","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543718,"source":"dbSNP","strand":1,"feature_type":"variation","end":140543718,"alleles":["T","C"],"seq_region_name":"7","id":"rs1316817091","clinical_significance":[]},{"start":140543719,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140543719,"strand":1,"feature_type":"variation","id":"rs892457077","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140543724,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543724,"source":"dbSNP","seq_region_name":"7","id":"rs1050188437","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140543728,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543728,"source":"dbSNP","seq_region_name":"7","id":"rs1796776555","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543729,"feature_type":"variation","strand":1,"end":140543729,"alleles":["G","T"],"clinical_significance":[],"id":"rs1267258804","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1357398057","source":"dbSNP","start":140543730,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140543730,"alleles":["A","G"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140543731,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543731,"source":"dbSNP","seq_region_name":"7","id":"rs1221949140","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796777305","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543737,"source":"dbSNP","strand":1,"feature_type":"variation","end":140543737,"alleles":["G","C"]},{"seq_region_name":"7","id":"rs888830960","clinical_significance":[],"end":140543739,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140543739,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1796777681","clinical_significance":[],"end":140543740,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140543740,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1484193660","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543741,"feature_type":"variation","strand":1,"end":140543741,"alleles":["A","C","G"]},{"seq_region_name":"7","id":"rs540741001","clinical_significance":[],"start":140543742,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140543742,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"start":140543743,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140543743,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1021412109","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130519207","clinical_significance":[],"strand":1,"feature_type":"variation","end":140543744,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543744,"source":"dbSNP"},{"id":"rs1796778490","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543745,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140543745},{"clinical_significance":[],"seq_region_name":"7","id":"rs565200479","feature_type":"variation","strand":1,"end":140543747,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543747},{"clinical_significance":[],"seq_region_name":"7","id":"rs903132318","source":"dbSNP","start":140543749,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140543749,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1306495583","source":"dbSNP","start":140543750,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140543750,"feature_type":"variation","strand":1},{"alleles":["C","G"],"end":140543753,"feature_type":"variation","strand":1,"source":"dbSNP","start":140543753,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1429497623"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1366652244","source":"dbSNP","start":140543754,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140543754,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543757,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140543757,"id":"rs1046517905","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140543761,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TTTTT","TTTT"],"end":140543765,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1189567486"},{"alleles":["G","A"],"end":140543766,"strand":1,"feature_type":"variation","start":140543766,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs189653094","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140543767,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543767,"clinical_significance":[],"seq_region_name":"7","id":"rs550945897"},{"seq_region_name":"7","id":"rs1470440453","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140543768,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543768,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543769,"feature_type":"variation","strand":1,"alleles":["TTTTT","TTTT"],"end":140543773,"clinical_significance":[],"seq_region_name":"7","id":"rs1796779931"},{"seq_region_name":"7","id":"rs111882595","clinical_significance":[],"alleles":["C","T"],"end":140543776,"strand":1,"feature_type":"variation","start":140543776,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140543779,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543779,"source":"dbSNP","seq_region_name":"7","id":"rs1203023798","clinical_significance":[]},{"start":140543781,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140543781,"alleles":["A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs953014798","clinical_significance":[]},{"source":"dbSNP","start":140543782,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140543782,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1168751313"},{"id":"rs530458387","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140543783,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543783,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1796780593","clinical_significance":[],"end":140543785,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140543785,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543786,"feature_type":"variation","strand":1,"end":140543786,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585590552"},{"seq_region_name":"7","id":"rs1223984699","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543787,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140543787},{"source":"dbSNP","start":140543790,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140543790,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1796780949","seq_region_name":"7"},{"source":"dbSNP","start":140543791,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140543791,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796781058"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796781172","source":"dbSNP","start":140543793,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140543793,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1023754295","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140543796,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543796},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140543797,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543797,"source":"dbSNP","seq_region_name":"7","id":"rs1796781422","clinical_significance":[]},{"id":"rs1320172743","seq_region_name":"7","clinical_significance":[],"start":140543803,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140543803,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140543804,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543804,"clinical_significance":[],"seq_region_name":"7","id":"rs2130519455"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140543805,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543805,"clinical_significance":[],"seq_region_name":"7","id":"rs1372003713"},{"seq_region_name":"7","id":"rs1796781757","clinical_significance":[],"start":140543806,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140543806,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796781876","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140543807,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543807},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543809,"feature_type":"variation","strand":1,"end":140543809,"alleles":["G","C","T"],"clinical_significance":[],"id":"rs187745416","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140543815,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543815,"source":"dbSNP","seq_region_name":"7","id":"rs1006213701","clinical_significance":[]},{"id":"rs2130519510","seq_region_name":"7","clinical_significance":[],"start":140543817,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140543817,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"id":"rs1796782238","seq_region_name":"7","clinical_significance":[],"start":140543820,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140543820,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543823,"feature_type":"variation","strand":1,"end":140543823,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585590612"},{"clinical_significance":[],"id":"rs1375690422","seq_region_name":"7","end":140543824,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140543824,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs374448593","end":140543827,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140543827,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140543835,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140543835,"alleles":["A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585590627","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796783199","clinical_significance":[],"strand":1,"feature_type":"variation","end":140543836,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543836,"source":"dbSNP"},{"alleles":["C","T"],"end":140543837,"strand":1,"feature_type":"variation","start":140543837,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1427473160","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs558851313","end":140543838,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140543838,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs367778310","clinical_significance":[],"end":140543839,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140543839,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1305373587","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140543843,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543843,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140543844,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543844,"clinical_significance":[],"id":"rs182469525","seq_region_name":"7"},{"end":140543861,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140543861,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs577057964"},{"end":140543866,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140543866,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796784756"},{"end":140543870,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140543870,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796784941","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1163710198","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140543874,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543874},{"end":140543876,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140543876,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1315453796","clinical_significance":[]},{"seq_region_name":"7","id":"rs1381310878","clinical_significance":[],"alleles":["C","T"],"end":140543877,"strand":1,"feature_type":"variation","start":140543877,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140543879,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140543879,"strand":1,"feature_type":"variation","id":"rs1796785696","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","T"],"end":140543880,"strand":1,"feature_type":"variation","start":140543880,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs144349381","seq_region_name":"7","clinical_significance":[]},{"end":140543883,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140543883,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs923038116","clinical_significance":[]},{"source":"dbSNP","start":140543884,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140543884,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs112290170"},{"clinical_significance":[],"id":"rs1796786617","seq_region_name":"7","source":"dbSNP","start":140543885,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140543885,"feature_type":"variation","strand":1},{"end":140543891,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140543891,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs986008123","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796786941","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543894,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TTTTATTTTTATTTTT","TTTTATTTTT"],"end":140543909},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140543898,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543898,"source":"dbSNP","seq_region_name":"7","id":"rs1192708354","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs201072316","feature_type":"variation","strand":1,"end":140543903,"alleles":["TTTTT","TTTT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543899},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140543905,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543905,"clinical_significance":[],"seq_region_name":"7","id":"rs1796787559"},{"clinical_significance":[],"id":"rs1246329793","seq_region_name":"7","feature_type":"variation","strand":1,"end":140543907,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543907},{"clinical_significance":[],"seq_region_name":"7","id":"rs1216858755","alleles":["G","A"],"end":140543912,"feature_type":"variation","strand":1,"source":"dbSNP","start":140543912,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1796787895","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140543914,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543914,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1250507770","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140543919,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543919,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1331287141","source":"dbSNP","start":140543920,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140543920,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs923481796","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543921,"feature_type":"variation","strand":1,"end":140543921,"alleles":["T","G"]},{"end":140543922,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140543922,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1796788339","seq_region_name":"7"},{"end":140543926,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140543926,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1796788459","seq_region_name":"7"},{"start":140543936,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C"],"end":140543936,"strand":1,"feature_type":"variation","id":"rs571217311","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543944,"feature_type":"variation","strand":1,"end":140543944,"alleles":["T","C"],"clinical_significance":[],"id":"rs1796788718","seq_region_name":"7"},{"end":140543948,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140543948,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1324894687"},{"seq_region_name":"7","id":"rs1796788969","clinical_significance":[],"alleles":["T","C"],"end":140543949,"strand":1,"feature_type":"variation","start":140543949,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140543950,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543950,"clinical_significance":[],"seq_region_name":"7","id":"rs1796789090"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140543952,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543952,"clinical_significance":[],"seq_region_name":"7","id":"rs1585590842"},{"source":"dbSNP","start":140543954,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140543954,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1448533488"},{"start":140543955,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140543955,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs566538615","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1367429592","alleles":["A","G"],"end":140543961,"feature_type":"variation","strand":1,"source":"dbSNP","start":140543961,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140543970,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140543970,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs933012688","seq_region_name":"7"},{"start":140543977,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140543977,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1483464181","clinical_significance":[]},{"clinical_significance":[],"id":"rs1431079926","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543982,"feature_type":"variation","strand":1,"end":140543982,"alleles":["C","T"]},{"strand":1,"feature_type":"variation","end":140543983,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543983,"source":"dbSNP","seq_region_name":"7","id":"rs1796790035","clinical_significance":[]},{"source":"dbSNP","start":140543984,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140543984,"alleles":["T","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585590901"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1390136780","feature_type":"variation","strand":1,"end":140543987,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543987},{"seq_region_name":"7","id":"rs1202047281","clinical_significance":[],"start":140543990,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140543990,"strand":1,"feature_type":"variation"},{"start":140543991,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140543991,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1253989073","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs187119734","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140543994,"feature_type":"variation","strand":1,"alleles":["C","A","G","T"],"end":140543994},{"strand":1,"feature_type":"variation","end":140543995,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140543995,"source":"dbSNP","seq_region_name":"7","id":"rs1796790699","clinical_significance":[]},{"seq_region_name":"7","id":"rs1429920994","clinical_significance":[],"end":140544004,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","start":140544004,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1178215206","end":140544005,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140544005,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544006,"feature_type":"variation","strand":1,"end":140544006,"alleles":["C","T"],"clinical_significance":[],"id":"rs2130520072","seq_region_name":"7"},{"clinical_significance":[],"id":"rs2130520083","seq_region_name":"7","feature_type":"variation","strand":1,"end":140544019,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544019},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544022,"feature_type":"variation","strand":1,"end":140544022,"alleles":["G","A"],"clinical_significance":[],"id":"rs1796791081","seq_region_name":"7"},{"alleles":["G","A"],"end":140544025,"strand":1,"feature_type":"variation","start":140544025,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796791202","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796791326","clinical_significance":[],"start":140544027,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140544027,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544028,"feature_type":"variation","strand":1,"end":140544028,"alleles":["G","-"],"clinical_significance":[],"seq_region_name":"7","id":"rs1796791418"},{"end":140544032,"alleles":["C","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140544032,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs751519984"},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140544032,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544032,"source":"dbSNP","seq_region_name":"7","id":"rs1585590960","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130520137","clinical_significance":[],"alleles":["C","-"],"end":140544036,"strand":1,"feature_type":"variation","start":140544036,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140544038,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544038,"source":"dbSNP","id":"rs556577075","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs574876241","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544039,"feature_type":"variation","strand":1,"end":140544039,"alleles":["G","A"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544041,"source":"dbSNP","strand":1,"feature_type":"variation","end":140544041,"alleles":["G","C"],"seq_region_name":"7","id":"rs1796791928","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140544045,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544045,"source":"dbSNP","seq_region_name":"7","id":"rs1187307912","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140544047,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544047,"clinical_significance":[],"id":"rs749606991","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1042901176","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544048,"feature_type":"variation","strand":1,"end":140544048,"alleles":["T","A","G"]},{"seq_region_name":"7","id":"rs116428677","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544050,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140544050},{"alleles":["G","A"],"end":140544057,"feature_type":"variation","strand":1,"source":"dbSNP","start":140544057,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130520221"},{"alleles":["T","A"],"end":140544062,"feature_type":"variation","strand":1,"source":"dbSNP","start":140544062,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1258284078"},{"end":140544064,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140544064,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs554413072"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544065,"feature_type":"variation","strand":1,"end":140544065,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1311955830"},{"clinical_significance":[],"seq_region_name":"7","id":"rs938058723","feature_type":"variation","strand":1,"end":140544077,"alleles":["A","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544077},{"clinical_significance":[],"id":"rs1228627441","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140544078,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544078},{"clinical_significance":[],"seq_region_name":"7","id":"rs115791732","source":"dbSNP","start":140544081,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140544081,"alleles":["T","C","G"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544084,"source":"dbSNP","strand":1,"feature_type":"variation","end":140544084,"alleles":["G","A"],"id":"rs1796793596","seq_region_name":"7","clinical_significance":[]},{"id":"rs1796793709","seq_region_name":"7","clinical_significance":[],"start":140544102,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140544102,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs888604094","clinical_significance":[],"start":140544103,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140544103,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"id":"rs1433693413","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544104,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140544104},{"seq_region_name":"7","id":"rs1406255507","clinical_significance":[],"start":140544106,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140544106,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"start":140544108,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140544108,"strand":1,"feature_type":"variation","id":"rs1585591129","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1005684666","alleles":["T","C","G"],"end":140544111,"feature_type":"variation","strand":1,"source":"dbSNP","start":140544111,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140544112,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544112,"clinical_significance":[],"seq_region_name":"7","id":"rs1796794489"},{"end":140544120,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140544120,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796794608","clinical_significance":[]},{"clinical_significance":[],"id":"rs1796794724","seq_region_name":"7","alleles":["C","T"],"end":140544122,"feature_type":"variation","strand":1,"source":"dbSNP","start":140544122,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140544123,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140544123,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs1016279795","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs895714214","end":140544130,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140544130,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796795055","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140544132,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544132},{"seq_region_name":"7","id":"rs1796795152","clinical_significance":[],"alleles":["C","G"],"end":140544133,"strand":1,"feature_type":"variation","start":140544133,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1013626380","clinical_significance":[],"end":140544134,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140544134,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544135,"source":"dbSNP","strand":1,"feature_type":"variation","end":140544135,"alleles":["G","A"],"seq_region_name":"7","id":"rs1024036649","clinical_significance":[]},{"seq_region_name":"7","id":"rs1170883857","clinical_significance":[],"end":140544143,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140544143,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140544144,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140544144,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs201527589"},{"seq_region_name":"7","id":"rs1796795777","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544151,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140544151},{"seq_region_name":"7","id":"rs1388537398","clinical_significance":[],"start":140544152,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140544152,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140544157,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544157,"clinical_significance":[],"seq_region_name":"7","id":"rs1188245020"},{"strand":1,"feature_type":"variation","end":140544160,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544160,"source":"dbSNP","seq_region_name":"7","id":"rs1796796113","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544165,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140544165,"clinical_significance":[],"seq_region_name":"7","id":"rs1796796229"},{"start":140544167,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140544167,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1445283499","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544170,"feature_type":"variation","strand":1,"end":140544170,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1466877961"},{"end":140544171,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140544171,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1563128826"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544172,"source":"dbSNP","strand":1,"feature_type":"variation","end":140544172,"alleles":["A","G"],"id":"rs141414846","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140544172,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140544172,"alleles":["A","AA"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1199199485"},{"start":140544174,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140544174,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130520536","clinical_significance":[]},{"start":140544181,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140544181,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1404513346","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544182,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140544182,"id":"rs1452601536","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1340553623","clinical_significance":[],"strand":1,"feature_type":"variation","end":140544196,"alleles":["CCTGGCCATCCT","CCT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544185,"source":"dbSNP"},{"clinical_significance":[],"id":"rs565382944","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544191,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140544191},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140544193,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544193,"source":"dbSNP","seq_region_name":"7","id":"rs1029937600","clinical_significance":[]},{"start":140544199,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140544199,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1227262347","clinical_significance":[]},{"clinical_significance":[],"id":"rs1796797619","seq_region_name":"7","feature_type":"variation","strand":1,"end":140544201,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544201},{"clinical_significance":[],"id":"rs2130520608","seq_region_name":"7","feature_type":"variation","strand":1,"end":140544203,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544203},{"clinical_significance":[],"seq_region_name":"7","id":"rs1016331145","alleles":["T","G"],"end":140544204,"feature_type":"variation","strand":1,"source":"dbSNP","start":140544204,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1796797820","clinical_significance":[],"strand":1,"feature_type":"variation","end":140544205,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544205,"source":"dbSNP"},{"alleles":["GGGGC","-"],"end":140544210,"strand":1,"feature_type":"variation","start":140544206,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs2130520627","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","A"],"end":140544207,"strand":1,"feature_type":"variation","start":140544207,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1796797922","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1321257479","source":"dbSNP","start":140544208,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140544208,"feature_type":"variation","strand":1},{"alleles":["G","C"],"end":140544209,"feature_type":"variation","strand":1,"source":"dbSNP","start":140544209,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130520651"},{"seq_region_name":"7","id":"rs1340526361","clinical_significance":[],"strand":1,"feature_type":"variation","end":140544210,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544210,"source":"dbSNP"},{"alleles":["G","T"],"end":140544212,"feature_type":"variation","strand":1,"source":"dbSNP","start":140544212,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1796798235","seq_region_name":"7"},{"clinical_significance":[],"id":"rs2130520674","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544212,"feature_type":"variation","strand":1,"end":140544213,"alleles":["GG","G"]},{"start":140544215,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140544215,"strand":1,"feature_type":"variation","id":"rs1796798334","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","A"],"end":140544217,"feature_type":"variation","strand":1,"source":"dbSNP","start":140544217,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796798421"},{"seq_region_name":"7","id":"rs2130520699","clinical_significance":[],"alleles":["AG","-"],"end":140544220,"strand":1,"feature_type":"variation","start":140544219,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs533858375","source":"dbSNP","start":140544221,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140544221,"alleles":["G","T"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544222,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140544222,"clinical_significance":[],"seq_region_name":"7","id":"rs986277086"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130520735","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544226,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140544226},{"source":"dbSNP","start":140544227,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140544227,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796798766"},{"source":"dbSNP","start":140544235,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140544235,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs972610551"},{"source":"dbSNP","start":140544236,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140544236,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1796798988","seq_region_name":"7"},{"end":140544238,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140544238,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1796799152","seq_region_name":"7"},{"clinical_significance":[],"id":"rs923582272","seq_region_name":"7","feature_type":"variation","strand":1,"end":140544239,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544239},{"clinical_significance":[],"id":"rs1394151845","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["AGCTGGAG","AG"],"end":140544246,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544239},{"clinical_significance":[],"id":"rs1796799671","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544241,"feature_type":"variation","strand":1,"end":140544241,"alleles":["C","G"]},{"alleles":["G","A"],"end":140544243,"feature_type":"variation","strand":1,"source":"dbSNP","start":140544243,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1017322434","seq_region_name":"7"},{"seq_region_name":"7","id":"rs955128279","clinical_significance":[],"end":140544246,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140544246,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1796800214","clinical_significance":[],"strand":1,"feature_type":"variation","end":140544248,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544248,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140544254,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544254,"clinical_significance":[],"seq_region_name":"7","id":"rs1563128893"},{"clinical_significance":[],"id":"rs1796800530","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544258,"feature_type":"variation","strand":1,"end":140544258,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796800690","feature_type":"variation","strand":1,"end":140544268,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544268},{"clinical_significance":[],"seq_region_name":"7","id":"rs1368522588","feature_type":"variation","strand":1,"end":140544274,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544274},{"clinical_significance":[],"id":"rs1796800938","seq_region_name":"7","alleles":["A","G"],"end":140544275,"feature_type":"variation","strand":1,"source":"dbSNP","start":140544275,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140544278,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140544278,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1796801029","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140544280,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544280,"source":"dbSNP","id":"rs2130520876","seq_region_name":"7","clinical_significance":[]},{"start":140544281,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140544281,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","id":"rs1585591480","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140544282,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544282,"source":"dbSNP","seq_region_name":"7","id":"rs958111262","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1235122107","source":"dbSNP","start":140544285,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140544285,"alleles":["C","A"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140544287,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544287,"source":"dbSNP","seq_region_name":"7","id":"rs1585591517","clinical_significance":[]},{"alleles":["A","G"],"end":140544288,"feature_type":"variation","strand":1,"source":"dbSNP","start":140544288,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1796801568","seq_region_name":"7"},{"end":140544289,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140544289,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs371222185","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140544290,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544290,"clinical_significance":[],"seq_region_name":"7","id":"rs1796801782"},{"id":"rs1460790294","seq_region_name":"7","clinical_significance":[],"start":140544295,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140544295,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1185507847","feature_type":"variation","strand":1,"end":140544297,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544297},{"strand":1,"feature_type":"variation","end":140544298,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544298,"source":"dbSNP","seq_region_name":"7","id":"rs1423679992","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544300,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140544300,"clinical_significance":[],"seq_region_name":"7","id":"rs910206400"},{"start":140544301,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140544301,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796802354","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1185056227","alleles":["C","T"],"end":140544302,"feature_type":"variation","strand":1,"source":"dbSNP","start":140544302,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140544303,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544303,"source":"dbSNP","seq_region_name":"7","id":"rs1796802577","clinical_significance":[]},{"id":"rs544709924","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544304,"source":"dbSNP","strand":1,"feature_type":"variation","end":140544304,"alleles":["C","G","T"]},{"source":"dbSNP","start":140544305,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140544305,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs947025199"},{"clinical_significance":[],"id":"rs1796802981","seq_region_name":"7","alleles":["G","A"],"end":140544307,"feature_type":"variation","strand":1,"source":"dbSNP","start":140544307,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140544309,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140544309,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796803096"},{"seq_region_name":"7","id":"rs2130521049","clinical_significance":[],"alleles":["T","C"],"end":140544310,"strand":1,"feature_type":"variation","start":140544310,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140544316,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140544316,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130521055","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544317,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140544317,"clinical_significance":[],"seq_region_name":"7","id":"rs1796803179"},{"clinical_significance":[],"id":"rs1796803290","seq_region_name":"7","end":140544320,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140544320,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs772203845","clinical_significance":[],"strand":1,"feature_type":"variation","end":140544321,"alleles":["A","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544321,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1249292333","seq_region_name":"7","source":"dbSNP","start":140544329,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140544329,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140544330,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544330,"clinical_significance":[],"seq_region_name":"7","id":"rs1796803690"},{"start":140544331,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140544331,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585591629","clinical_significance":[]},{"start":140544333,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140544333,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796803923","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544339,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140544339,"clinical_significance":[],"seq_region_name":"7","id":"rs143952131"},{"clinical_significance":[],"seq_region_name":"7","id":"rs530095735","source":"dbSNP","start":140544340,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140544340,"alleles":["G","A","C"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140544348,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544348,"source":"dbSNP","seq_region_name":"7","id":"rs1796804322","clinical_significance":[]},{"seq_region_name":"7","id":"rs1339437841","clinical_significance":[],"start":140544349,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140544349,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544351,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140544351,"id":"rs2130521168","seq_region_name":"7","clinical_significance":[]},{"id":"rs1288879409","seq_region_name":"7","clinical_significance":[],"start":140544353,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140544353,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs555647061","clinical_significance":[],"end":140544354,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140544354,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140544356,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140544356,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1434596053","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796804904","source":"dbSNP","start":140544362,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TTTTT","TTTT"],"end":140544366,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796805007","source":"dbSNP","start":140544369,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140544369,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796805123","feature_type":"variation","strand":1,"end":140544374,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544374},{"seq_region_name":"7","id":"rs934528766","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544375,"source":"dbSNP","strand":1,"feature_type":"variation","end":140544375,"alleles":["A","G"]},{"feature_type":"variation","strand":1,"end":140544376,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544376,"clinical_significance":[],"seq_region_name":"7","id":"rs1057362790"},{"source":"dbSNP","start":140544379,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140544379,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1307221062"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544380,"feature_type":"variation","strand":1,"end":140544380,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1796805590"},{"end":140544383,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140544383,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1427678285","clinical_significance":[]},{"seq_region_name":"7","id":"rs551618241","clinical_significance":[],"alleles":["G","A","C"],"end":140544384,"strand":1,"feature_type":"variation","start":140544384,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1161734539","feature_type":"variation","strand":1,"end":140544386,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544386},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544387,"source":"dbSNP","strand":1,"feature_type":"variation","end":140544387,"alleles":["G","C"],"seq_region_name":"7","id":"rs895756341","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796806267","source":"dbSNP","start":140544392,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140544392,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140544395,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140544395,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs982132169"},{"seq_region_name":"7","id":"rs927948166","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544396,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140544396},{"clinical_significance":[],"seq_region_name":"7","id":"rs1428721522","source":"dbSNP","start":140544399,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140544399,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140544402,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544402,"clinical_significance":[],"seq_region_name":"7","id":"rs1251496469"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544403,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140544403,"seq_region_name":"7","id":"rs1796806877","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs760747520","alleles":["C","T"],"end":140544407,"feature_type":"variation","strand":1,"source":"dbSNP","start":140544407,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140544414,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140544414,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1288422524","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1453747101","alleles":["G","A"],"end":140544415,"feature_type":"variation","strand":1,"source":"dbSNP","start":140544415,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1796807353","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544416,"feature_type":"variation","strand":1,"end":140544416,"alleles":["A","G"]},{"start":140544420,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140544420,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1269016831","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544422,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140544422,"clinical_significance":[],"id":"rs1796807563","seq_region_name":"7"},{"seq_region_name":"7","id":"rs765152247","clinical_significance":[],"strand":1,"feature_type":"variation","end":140544423,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544423,"source":"dbSNP"},{"source":"dbSNP","start":140544425,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140544425,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs114350181","seq_region_name":"7"},{"start":140544434,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140544434,"alleles":["A","T"],"strand":1,"feature_type":"variation","id":"rs1281091476","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1268240778","seq_region_name":"7","alleles":["T","C"],"end":140544435,"feature_type":"variation","strand":1,"source":"dbSNP","start":140544435,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140544436,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544436,"clinical_significance":[],"seq_region_name":"7","id":"rs1006185044"},{"seq_region_name":"7","id":"rs1796808363","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544437,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140544437},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585591885","end":140544438,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140544438,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140544441,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140544441,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796808631","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544442,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140544442,"clinical_significance":[],"seq_region_name":"7","id":"rs1585591895"},{"id":"rs1796808868","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140544443,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544443,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544444,"source":"dbSNP","strand":1,"feature_type":"variation","end":140544444,"alleles":["C","G"],"seq_region_name":"7","id":"rs1327007309","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544453,"feature_type":"variation","strand":1,"end":140544453,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1796809090"},{"source":"dbSNP","start":140544461,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","-"],"end":140544461,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796809211"},{"strand":1,"feature_type":"variation","end":140544464,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544464,"source":"dbSNP","id":"rs1796809340","seq_region_name":"7","clinical_significance":[]},{"id":"rs1796809450","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544468,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140544468},{"seq_region_name":"7","id":"rs1585591910","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140544470,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544470,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1016367484","end":140544471,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140544471,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1563129021","seq_region_name":"7","clinical_significance":[],"alleles":["G","A","C","T"],"end":140544473,"strand":1,"feature_type":"variation","start":140544473,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["T","C"],"end":140544474,"feature_type":"variation","strand":1,"source":"dbSNP","start":140544474,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1796809953","seq_region_name":"7"},{"start":140544476,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140544476,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585591937","clinical_significance":[]},{"seq_region_name":"7","id":"rs1322581787","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544477,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140544477},{"source":"dbSNP","start":140544479,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140544479,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1287419088"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140544484,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544484,"clinical_significance":[],"seq_region_name":"7","id":"rs962114250"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544485,"source":"dbSNP","strand":1,"feature_type":"variation","end":140544485,"alleles":["G","A","T"],"seq_region_name":"7","id":"rs114896251","clinical_significance":[]},{"alleles":["C","T"],"end":140544486,"strand":1,"feature_type":"variation","start":140544486,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs146417383","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1386469697","end":140544487,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140544487,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544489,"feature_type":"variation","strand":1,"alleles":["C","A","G"],"end":140544489,"clinical_significance":[],"seq_region_name":"7","id":"rs1796811062"},{"start":140544491,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140544491,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796811202","clinical_significance":[]},{"id":"rs1214434261","seq_region_name":"7","clinical_significance":[],"end":140544494,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140544494,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs955012657","feature_type":"variation","strand":1,"end":140544499,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544499},{"seq_region_name":"7","id":"rs1796811548","clinical_significance":[],"alleles":["C","T"],"end":140544500,"strand":1,"feature_type":"variation","start":140544500,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140544501,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140544501,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs986802009","clinical_significance":[]},{"start":140544514,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140544514,"alleles":["A","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1411858108","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140544515,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544515,"clinical_significance":[],"seq_region_name":"7","id":"rs1796811938"},{"clinical_significance":[],"id":"rs1796812048","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544518,"feature_type":"variation","strand":1,"end":140544518,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1173745163","clinical_significance":[],"strand":1,"feature_type":"variation","end":140544519,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544519,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1164311609","seq_region_name":"7","end":140544523,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140544523,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140544524,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140544524,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs773650633"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140544525,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544525,"source":"dbSNP","seq_region_name":"7","id":"rs1433664162","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544529,"source":"dbSNP","strand":1,"feature_type":"variation","end":140544529,"alleles":["A","G"],"seq_region_name":"7","id":"rs1796812643","clinical_significance":[]},{"alleles":["A","C"],"end":140544530,"strand":1,"feature_type":"variation","start":140544530,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585592087","clinical_significance":[]},{"end":140544532,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140544532,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1376336779","clinical_significance":[]},{"end":140544534,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140544534,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs149042446"},{"clinical_significance":[],"id":"rs752694952","seq_region_name":"7","feature_type":"variation","strand":1,"end":140544535,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544535},{"seq_region_name":"7","id":"rs766715009","clinical_significance":[],"end":140544538,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140544538,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140544539,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140544539,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1225288890","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544543,"feature_type":"variation","strand":1,"end":140544543,"alleles":["A","C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs776794859"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1328409991","source":"dbSNP","start":140544545,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140544545,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs556614466","clinical_significance":[],"start":140544548,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140544548,"strand":1,"feature_type":"variation"},{"end":140544550,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140544550,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs765479263","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544552,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140544552,"seq_region_name":"7","id":"rs751419622","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1220900503","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544553,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140544553},{"start":140544555,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140544555,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796814207","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1300073110","end":140544556,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140544556,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs2130521977","seq_region_name":"7","alleles":["T","A"],"end":140544558,"feature_type":"variation","strand":1,"source":"dbSNP","start":140544558,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140544559,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140544559,"alleles":["A","G"],"strand":1,"feature_type":"variation","id":"rs757266338","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1481716417","feature_type":"variation","strand":1,"end":140544560,"alleles":["G","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544560},{"clinical_significance":[],"seq_region_name":"7","id":"rs1267420072","end":140544561,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140544561,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1796814824","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140544562,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544562,"source":"dbSNP"},{"seq_region_name":"7","id":"rs998392142","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140544563,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544563,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs375815461","feature_type":"variation","strand":1,"end":140544566,"alleles":["C","A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544566},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796815222","alleles":["C","T"],"end":140544567,"feature_type":"variation","strand":1,"source":"dbSNP","start":140544567,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["CAAGAGCGACTGTCATTCAA","CAA"],"end":140544586,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544567,"source":"dbSNP","seq_region_name":"7","id":"rs764624684","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs767166662","feature_type":"variation","strand":1,"end":140544569,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544569},{"clinical_significance":[],"seq_region_name":"7","id":"rs750260967","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544570,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140544570},{"clinical_significance":[],"seq_region_name":"7","id":"rs372848853","source":"dbSNP","start":140544573,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140544573,"alleles":["C","T"],"feature_type":"variation","strand":1},{"start":140544574,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C","T"],"end":140544574,"strand":1,"feature_type":"variation","id":"rs375246547","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140544577,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544577,"clinical_significance":[],"id":"rs1403141416","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544578,"feature_type":"variation","strand":1,"end":140544578,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1163417174"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1277396849","feature_type":"variation","strand":1,"end":140544582,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544582},{"clinical_significance":[],"seq_region_name":"7","id":"rs752050225","feature_type":"variation","strand":1,"alleles":["AAA","AA"],"end":140544587,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544585},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140544588,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544588,"clinical_significance":[],"seq_region_name":"7","id":"rs369271982"},{"clinical_significance":[],"seq_region_name":"7","id":"rs917080436","source":"dbSNP","start":140544589,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140544589,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs535809452","alleles":["C","G","T"],"end":140544590,"feature_type":"variation","strand":1,"source":"dbSNP","start":140544590,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140544594,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140544594,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1044705609"},{"source":"dbSNP","start":140544595,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140544595,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs372556060"},{"alleles":["C","G"],"end":140544606,"feature_type":"variation","strand":1,"source":"dbSNP","start":140544606,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1335426350"},{"start":140544610,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_region_variant","alleles":["G","A"],"end":140544610,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs772667915","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs773384220","feature_type":"variation","strand":1,"end":140544611,"alleles":["C","A","T"],"consequence_type":"splice_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544611},{"source":"dbSNP","start":140544612,"consequence_type":"splice_donor_region_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140544612,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs377539073"},{"source":"dbSNP","start":140544614,"consequence_type":"splice_donor_region_variant","assembly_name":"GRCh38","end":140544614,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1227838778"},{"alleles":["C","T"],"end":140544618,"strand":1,"feature_type":"variation","start":140544618,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs776989363","clinical_significance":[]},{"source":"dbSNP","start":140544619,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140544619,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1563129195"},{"seq_region_name":"7","id":"rs1796818269","clinical_significance":[],"end":140544622,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140544622,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544623,"feature_type":"variation","strand":1,"end":140544623,"alleles":["C","G"],"clinical_significance":[],"id":"rs1309493744","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140544632,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140544632,"seq_region_name":"7","id":"rs1219653930","clinical_significance":["uncertain significance"]},{"feature_type":"variation","strand":1,"end":140544633,"alleles":["A","G"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544633,"clinical_significance":["uncertain significance"],"seq_region_name":"7","id":"rs759877921"},{"end":140544634,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140544634,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1251348017"},{"source":"dbSNP","start":140544637,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140544637,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs765384485"},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140544643,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140544643,"id":"rs1453366896","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs775660045","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140544644,"source":"dbSNP","strand":1,"feature_type":"variation","end":140544644,"alleles":["C","T"]},{"id":"rs1796819302","seq_region_name":"7","clinical_significance":[],"start":140544647,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["C","A"],"end":140544647,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796819439","source":"dbSNP","start":140544648,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140544648,"alleles":["C","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1236269317","clinical_significance":[],"start":140544656,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","end":140544656,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140544658,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140544658,"source":"dbSNP","seq_region_name":"7","id":"rs761613317","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1190181620","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140544667,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544667},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140544672,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140544672,"seq_region_name":"7","id":"rs371322544","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796820069","feature_type":"variation","strand":1,"end":140544673,"alleles":["C","G","T"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544673},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140544675,"source":"dbSNP","strand":1,"feature_type":"variation","end":140544675,"alleles":["C","G","T"],"seq_region_name":"7","id":"rs750124447","clinical_significance":[]},{"clinical_significance":[],"id":"rs1419523191","seq_region_name":"7","consequence_type":"frameshift_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544675,"feature_type":"variation","strand":1,"alleles":["C","-"],"end":140544675},{"clinical_significance":[],"seq_region_name":"7","id":"rs766206225","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544687,"feature_type":"variation","strand":1,"end":140544687,"alleles":["C","G","T"]},{"seq_region_name":"7","id":"rs1369531403","clinical_significance":[],"end":140544688,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140544688,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"strand":1,"feature_type":"variation","end":140544689,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140544689,"source":"dbSNP","seq_region_name":"7","id":"rs1563129301","clinical_significance":[]},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544691,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140544691,"clinical_significance":["uncertain significance"],"seq_region_name":"7","id":"rs374348351"},{"clinical_significance":[],"seq_region_name":"7","id":"rs778248524","feature_type":"variation","strand":1,"end":140544692,"alleles":["G","A"],"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544692},{"strand":1,"feature_type":"variation","end":140544694,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140544694,"source":"dbSNP","seq_region_name":"7","id":"rs573006048","clinical_significance":[]},{"alleles":["G","C"],"end":140544697,"feature_type":"variation","strand":1,"source":"dbSNP","start":140544697,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796821449"},{"source":"dbSNP","start":140544698,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140544698,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs758774823"},{"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544701,"feature_type":"variation","strand":1,"end":140544701,"alleles":["G","A"],"clinical_significance":[],"id":"rs199613064","seq_region_name":"7"},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544702,"feature_type":"variation","strand":1,"end":140544702,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs747537181"},{"id":"rs771391244","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140544707,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140544707},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796822214","alleles":["G","C"],"end":140544709,"feature_type":"variation","strand":1,"source":"dbSNP","start":140544709,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140544711,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140544711,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"clinical_significance":["uncertain significance"],"seq_region_name":"7","id":"rs781723195"},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140544712,"source":"dbSNP","strand":1,"feature_type":"variation","end":140544712,"alleles":["A","T"],"seq_region_name":"7","id":"rs770169272","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs775362534","end":140544713,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140544713,"consequence_type":"synonymous_variant","assembly_name":"GRCh38"},{"alleles":["T","A"],"end":140544714,"feature_type":"variation","strand":1,"source":"dbSNP","start":140544714,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1276878353"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585592866","source":"dbSNP","start":140544719,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140544719,"alleles":["G","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1442356581","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544721,"feature_type":"variation","strand":1,"end":140544721,"alleles":["C","A"]},{"feature_type":"variation","strand":1,"end":140544724,"alleles":["C","T"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544724,"clinical_significance":["uncertain significance"],"seq_region_name":"7","id":"rs374987769"},{"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544725,"feature_type":"variation","strand":1,"end":140544725,"alleles":["G","A"],"clinical_significance":[],"id":"rs1020779474","seq_region_name":"7"},{"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544728,"feature_type":"variation","strand":1,"end":140544728,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs768671981"},{"seq_region_name":"7","id":"rs773192248","clinical_significance":[],"end":140544730,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140544730,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"end":140544731,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140544731,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs760659617"},{"clinical_significance":[],"id":"rs1454407510","seq_region_name":"7","source":"dbSNP","start":140544735,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140544735,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140544736,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140544736,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs766117690"},{"seq_region_name":"7","id":"rs753667814","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140544738,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140544738},{"alleles":["G","A"],"end":140544745,"strand":1,"feature_type":"variation","start":140544745,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","id":"rs2130522811","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140544746,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","end":140544746,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs759124814"},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544747,"feature_type":"variation","strand":1,"end":140544747,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1318957498"},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140544750,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140544750,"seq_region_name":"7","id":"rs1390710116","clinical_significance":[]},{"start":140544751,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140544751,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs1433032642","seq_region_name":"7","clinical_significance":[]},{"id":"rs1796824917","seq_region_name":"7","clinical_significance":[],"start":140544752,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","alleles":["G","A"],"end":140544752,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2293177","alleles":["C","A","G","T"],"end":140544760,"feature_type":"variation","strand":1,"source":"dbSNP","start":140544760,"consequence_type":"stop_gained","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs370523306","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140544761,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140544761},{"source":"dbSNP","start":140544763,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140544763,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1235609864","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140544765,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140544765,"id":"rs752352375","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140544766,"source":"dbSNP","strand":1,"feature_type":"variation","end":140544766,"alleles":["C","T"],"seq_region_name":"7","id":"rs1344823092","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs757922808","source":"dbSNP","start":140544767,"consequence_type":"splice_acceptor_variant","assembly_name":"GRCh38","end":140544767,"alleles":["C","G"],"feature_type":"variation","strand":1},{"alleles":["T","C"],"end":140544768,"feature_type":"variation","strand":1,"source":"dbSNP","start":140544768,"consequence_type":"splice_acceptor_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1206065166"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1270618166","consequence_type":"splice_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544770,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140544770},{"seq_region_name":"7","id":"rs1463902645","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"splice_region_variant","start":140544771,"source":"dbSNP","strand":1,"feature_type":"variation","end":140544771,"alleles":["C","G"]},{"consequence_type":"splice_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544773,"feature_type":"variation","strand":1,"end":140544773,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1246812316"},{"seq_region_name":"7","id":"rs780999441","clinical_significance":[],"start":140544773,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_polypyrimidine_tract_variant","alleles":["GGG","GG"],"end":140544775,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1468643715","consequence_type":"splice_polypyrimidine_tract_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544775,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140544775},{"seq_region_name":"7","id":"rs1796826823","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"splice_polypyrimidine_tract_variant","start":140544777,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140544777},{"end":140544778,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140544778,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_polypyrimidine_tract_variant","seq_region_name":"7","id":"rs1200633204","clinical_significance":[]},{"start":140544783,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_polypyrimidine_tract_variant","alleles":["G","C"],"end":140544783,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs777189075","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs535124303","source":"dbSNP","start":140544784,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140544784,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1158893673","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544787,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140544787},{"alleles":["T","C"],"end":140544790,"feature_type":"variation","strand":1,"source":"dbSNP","start":140544790,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796827397"},{"start":140544794,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140544794,"strand":1,"feature_type":"variation","id":"rs1563129476","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1414126206","clinical_significance":[],"start":140544797,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140544797,"strand":1,"feature_type":"variation"},{"alleles":["G","A"],"end":140544798,"feature_type":"variation","strand":1,"source":"dbSNP","start":140544798,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs576953142","seq_region_name":"7"},{"id":"rs1319979351","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140544800,"strand":1,"feature_type":"variation","start":140544800,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544804,"feature_type":"variation","strand":1,"end":140544804,"alleles":["A","G"],"clinical_significance":[],"id":"rs1796827943","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1395400719","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140544805,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544805},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544806,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140544806,"clinical_significance":[],"seq_region_name":"7","id":"rs1388579835"},{"feature_type":"variation","strand":1,"end":140544808,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544808,"clinical_significance":[],"id":"rs1321885716","seq_region_name":"7"},{"seq_region_name":"7","id":"rs544747009","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140544809,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544809,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs781653466","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140544810,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544810},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796828737","source":"dbSNP","start":140544812,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140544812,"alleles":["A","G"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544814,"source":"dbSNP","strand":1,"feature_type":"variation","end":140544814,"alleles":["C","T"],"id":"rs1796828828","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140544818,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140544818,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs746236017"},{"source":"dbSNP","start":140544821,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140544821,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796829072"},{"strand":1,"feature_type":"variation","end":140544822,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544822,"source":"dbSNP","seq_region_name":"7","id":"rs1796829173","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796829276","source":"dbSNP","start":140544823,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TCACGGGTGTCGCAGTC","TC"],"end":140544839,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140544826,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140544826,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs990808887"},{"seq_region_name":"7","id":"rs2293176","clinical_significance":[],"alleles":["G","A"],"end":140544827,"strand":1,"feature_type":"variation","start":140544827,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140544829,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140544829,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1796829730","seq_region_name":"7"},{"source":"dbSNP","start":140544831,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140544831,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs574904106"},{"id":"rs374727247","seq_region_name":"7","clinical_significance":[],"start":140544833,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140544833,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs375674643","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","C","T"],"end":140544834,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544834,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544835,"source":"dbSNP","strand":1,"feature_type":"variation","end":140544835,"alleles":["C","T"],"seq_region_name":"7","id":"rs1377159083","clinical_significance":[]},{"source":"dbSNP","start":140544843,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140544843,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1177154613"},{"clinical_significance":[],"seq_region_name":"7","id":"rs369648120","source":"dbSNP","start":140544845,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140544845,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1037202765","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140544846,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544846},{"clinical_significance":[],"id":"rs1585593445","seq_region_name":"7","end":140544847,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140544847,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544853,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140544853,"seq_region_name":"7","id":"rs1352666371","clinical_significance":[]},{"id":"rs1796830806","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544860,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140544860},{"seq_region_name":"7","id":"rs1306599204","clinical_significance":[],"start":140544861,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140544861,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs955702457","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140544866,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544866,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140544868,"alleles":["GTG","GTGTG"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544866,"source":"dbSNP","seq_region_name":"7","id":"rs139394260","clinical_significance":[]},{"seq_region_name":"7","id":"rs767284493","clinical_significance":[],"end":140544872,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140544872,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140544873,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140544873,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796831379","clinical_significance":[]},{"source":"dbSNP","start":140544874,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140544874,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1796831493","seq_region_name":"7"},{"seq_region_name":"7","id":"rs560846768","clinical_significance":[],"end":140544877,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140544877,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs115579634","clinical_significance":[],"strand":1,"feature_type":"variation","end":140544878,"alleles":["T","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544878,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1365173574","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544879,"source":"dbSNP","strand":1,"feature_type":"variation","end":140544879,"alleles":["G","A","T"]},{"strand":1,"feature_type":"variation","end":140544883,"alleles":["GGGGG","GGGG"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544879,"source":"dbSNP","seq_region_name":"7","id":"rs1796832045","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544880,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140544880,"seq_region_name":"7","id":"rs1472893910","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140544881,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544881,"clinical_significance":[],"seq_region_name":"7","id":"rs1253618774"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140544882,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544882,"clinical_significance":[],"seq_region_name":"7","id":"rs1430690900"},{"start":140544884,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140544884,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1309580562","clinical_significance":[]},{"seq_region_name":"7","id":"rs1480218467","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544884,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AAAA","AAA"],"end":140544887},{"alleles":["A","G","T"],"end":140544886,"feature_type":"variation","strand":1,"source":"dbSNP","start":140544886,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs148213057"},{"seq_region_name":"7","id":"rs948566010","clinical_significance":[],"end":140544888,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140544888,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["A","G"],"end":140544893,"strand":1,"feature_type":"variation","start":140544893,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1051291081","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544895,"feature_type":"variation","strand":1,"alleles":["AAAAAAA","AAAAAA","AAAAAAAA"],"end":140544901,"clinical_significance":[],"id":"rs890018403","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796833018","alleles":["A","C"],"end":140544898,"feature_type":"variation","strand":1,"source":"dbSNP","start":140544898,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs564550547","seq_region_name":"7","source":"dbSNP","start":140544903,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140544903,"alleles":["C","A","G"],"feature_type":"variation","strand":1},{"id":"rs909841127","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140544914,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544914,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1228152263","clinical_significance":[],"start":140544915,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140544915,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs756106328","clinical_significance":[],"strand":1,"feature_type":"variation","end":140544916,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544916,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544918,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140544918,"clinical_significance":[],"seq_region_name":"7","id":"rs1381337391"},{"feature_type":"variation","strand":1,"end":140544919,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544919,"clinical_significance":[],"seq_region_name":"7","id":"rs1438196596"},{"seq_region_name":"7","id":"rs1796834280","clinical_significance":[],"end":140544927,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140544927,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1796834387","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544930,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140544930},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796834512","feature_type":"variation","strand":1,"alleles":["T","A"],"end":140544933,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544933},{"clinical_significance":[],"seq_region_name":"7","id":"rs1243123001","end":140544942,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140544942,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs116807966","clinical_significance":[],"start":140544943,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140544943,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs755746093","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140544944,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544944,"source":"dbSNP"},{"id":"rs893568880","seq_region_name":"7","clinical_significance":[],"start":140544944,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["GGGGGG","GGGGG","GGGGGGG"],"end":140544949,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1796835208","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544945,"source":"dbSNP","strand":1,"feature_type":"variation","end":140544945,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs550274512","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544946,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140544946},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544949,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140544949,"clinical_significance":[],"seq_region_name":"7","id":"rs1796835427"},{"clinical_significance":[],"id":"rs929300345","seq_region_name":"7","alleles":["C","G","T"],"end":140544950,"feature_type":"variation","strand":1,"source":"dbSNP","start":140544950,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["G","A"],"end":140544951,"feature_type":"variation","strand":1,"source":"dbSNP","start":140544951,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1275492370"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544956,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140544956,"id":"rs1436441463","seq_region_name":"7","clinical_significance":[]},{"end":140544957,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140544957,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs374480726","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544958,"feature_type":"variation","strand":1,"end":140544958,"alleles":["G","A"],"clinical_significance":[],"id":"rs1204356442","seq_region_name":"7"},{"seq_region_name":"7","id":"rs966541868","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544967,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140544967},{"start":140544970,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140544970,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1487647263","clinical_significance":[]},{"seq_region_name":"7","id":"rs1252381821","clinical_significance":[],"start":140544971,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140544971,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"alleles":["A","G"],"end":140544973,"strand":1,"feature_type":"variation","start":140544973,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1052285266","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs568571634","clinical_significance":[],"strand":1,"feature_type":"variation","end":140544974,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544974,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140544980,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544980,"source":"dbSNP","seq_region_name":"7","id":"rs2130523770","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544981,"feature_type":"variation","strand":1,"end":140544981,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs778406815"},{"source":"dbSNP","start":140544986,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140544986,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796836822"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544989,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140544989,"seq_region_name":"7","id":"rs531635366","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140544991,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140544991,"clinical_significance":[],"seq_region_name":"7","id":"rs1017708536"},{"alleles":["G","-"],"end":140544993,"feature_type":"variation","strand":1,"source":"dbSNP","start":140544993,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1239018106"},{"seq_region_name":"7","id":"rs74715338","clinical_significance":[],"strand":1,"feature_type":"variation","end":140544997,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140544997,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796837455","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140545000,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545000},{"start":140545003,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140545003,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796837570","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796838263","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140545011,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545011},{"clinical_significance":[],"id":"rs1450274413","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545018,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140545018},{"seq_region_name":"7","id":"rs1303900127","clinical_significance":[],"start":140545019,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140545019,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"alleles":["C","T"],"end":140545022,"feature_type":"variation","strand":1,"source":"dbSNP","start":140545022,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1000417284","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1365064682","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545023,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140545023},{"seq_region_name":"7","id":"rs1031858345","clinical_significance":[],"start":140545026,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140545026,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796838999","feature_type":"variation","strand":1,"end":140545032,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545032},{"seq_region_name":"7","id":"rs1302305131","clinical_significance":[],"end":140545038,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140545038,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140545047,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140545047,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796839213"},{"alleles":["A","G"],"end":140545048,"feature_type":"variation","strand":1,"source":"dbSNP","start":140545048,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs909882943"},{"end":140545050,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140545050,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1796839591","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs963155421","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545052,"feature_type":"variation","strand":1,"end":140545052,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs371878300","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545056,"feature_type":"variation","strand":1,"end":140545056,"alleles":["C","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545057,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140545057,"id":"rs779284239","seq_region_name":"7","clinical_significance":[]},{"end":140545058,"alleles":["GG","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140545057,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1452997284"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545058,"source":"dbSNP","strand":1,"feature_type":"variation","end":140545058,"alleles":["G","A","T"],"id":"rs1177975398","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","T"],"end":140545061,"strand":1,"feature_type":"variation","start":140545061,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs934180789","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1051175378","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545063,"feature_type":"variation","strand":1,"end":140545063,"alleles":["A","C"]},{"feature_type":"variation","strand":1,"end":140545064,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545064,"clinical_significance":[],"seq_region_name":"7","id":"rs1796840996"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545065,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140545065,"seq_region_name":"7","id":"rs992471482","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796841272","alleles":["T","C"],"end":140545066,"feature_type":"variation","strand":1,"source":"dbSNP","start":140545066,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1024511062","alleles":["G","T"],"end":140545067,"feature_type":"variation","strand":1,"source":"dbSNP","start":140545067,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs2130524033","clinical_significance":[],"alleles":["G","T"],"end":140545068,"strand":1,"feature_type":"variation","start":140545068,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585594115","end":140545069,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140545069,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs368852499","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545072,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140545072},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140545073,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545073,"source":"dbSNP","id":"rs76566834","seq_region_name":"7","clinical_significance":[]},{"start":140545079,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140545079,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585594156","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140545091,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545091,"clinical_significance":[],"seq_region_name":"7","id":"rs1796841987"},{"end":140545092,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140545092,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796842105"},{"clinical_significance":[],"seq_region_name":"7","id":"rs191896594","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545094,"feature_type":"variation","strand":1,"end":140545094,"alleles":["A","C","G"]},{"feature_type":"variation","strand":1,"end":140545095,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545095,"clinical_significance":[],"id":"rs1796842405","seq_region_name":"7"},{"source":"dbSNP","start":140545103,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140545103,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1208440607"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545106,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140545106,"clinical_significance":[],"seq_region_name":"7","id":"rs1796842642"},{"seq_region_name":"7","id":"rs941144781","clinical_significance":[],"end":140545108,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140545108,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["A","G"],"end":140545109,"feature_type":"variation","strand":1,"source":"dbSNP","start":140545109,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs972663512"},{"id":"rs576987863","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140545113,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545113,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545117,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TTTATAGGACTTT","TTTATAGGACTTTATAGGACTTT"],"end":140545129,"seq_region_name":"7","id":"rs1279120753","clinical_significance":[]},{"alleles":["T","C"],"end":140545121,"strand":1,"feature_type":"variation","start":140545121,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1228754566","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796843321","end":140545123,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140545123,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1796843427","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545125,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140545125},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563129775","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545127,"feature_type":"variation","strand":1,"end":140545130,"alleles":["TTTT","TTT"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545129,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140545129,"seq_region_name":"7","id":"rs116513581","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1292867105","alleles":["TG","TGTCCCTG"],"end":140545131,"feature_type":"variation","strand":1,"source":"dbSNP","start":140545130,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1381515325","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545132,"source":"dbSNP","strand":1,"feature_type":"variation","end":140545132,"alleles":["A","T"]},{"clinical_significance":[],"id":"rs1230080090","seq_region_name":"7","source":"dbSNP","start":140545133,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140545133,"alleles":["A","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1268049795","clinical_significance":[],"strand":1,"feature_type":"variation","end":140545137,"alleles":["ACG","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545135,"source":"dbSNP"},{"seq_region_name":"7","id":"rs556705994","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545136,"source":"dbSNP","strand":1,"feature_type":"variation","end":140545136,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1051767236","clinical_significance":[],"strand":1,"feature_type":"variation","end":140545137,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545137,"source":"dbSNP"},{"start":140545138,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140545138,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs572232668","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140545140,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545140,"source":"dbSNP","seq_region_name":"7","id":"rs1796844552","clinical_significance":[]},{"id":"rs1796844665","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140545144,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545144,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545146,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140545146,"seq_region_name":"7","id":"rs1431893754","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545153,"feature_type":"variation","strand":1,"end":140545153,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1388328467"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1192575348","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545155,"feature_type":"variation","strand":1,"end":140545155,"alleles":["C","A"]},{"end":140545160,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140545160,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1424527624","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796845219","clinical_significance":[],"end":140545161,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140545161,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["G","A"],"end":140545162,"feature_type":"variation","strand":1,"source":"dbSNP","start":140545162,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1258861911","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545167,"feature_type":"variation","strand":1,"end":140545167,"alleles":["C","T"],"clinical_significance":[],"id":"rs1003407317","seq_region_name":"7"},{"seq_region_name":"7","id":"rs772824784","clinical_significance":[],"start":140545169,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TCTCT","TCT"],"end":140545173,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs2130524403","clinical_significance":[],"alleles":["C","T"],"end":140545170,"strand":1,"feature_type":"variation","start":140545170,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140545172,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545172,"clinical_significance":[],"id":"rs1796845751","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1463015546","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545177,"source":"dbSNP","strand":1,"feature_type":"variation","end":140545177,"alleles":["T","C"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545178,"source":"dbSNP","strand":1,"feature_type":"variation","end":140545178,"alleles":["C","G"],"seq_region_name":"7","id":"rs2130524442","clinical_significance":[]},{"id":"rs1485539212","seq_region_name":"7","clinical_significance":[],"alleles":["G","C"],"end":140545184,"strand":1,"feature_type":"variation","start":140545184,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545191,"source":"dbSNP","strand":1,"feature_type":"variation","end":140545191,"alleles":["T","C"],"id":"rs1275831835","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140545192,"alleles":["A","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545192,"source":"dbSNP","id":"rs574941016","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1205383416","seq_region_name":"7","source":"dbSNP","start":140545192,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","AA"],"end":140545192,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1242551812","alleles":["T","C"],"end":140545195,"feature_type":"variation","strand":1,"source":"dbSNP","start":140545195,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1465406474","clinical_significance":[],"strand":1,"feature_type":"variation","end":140545200,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545200,"source":"dbSNP"},{"start":140545210,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140545210,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1039065708","clinical_significance":[]},{"clinical_significance":[],"id":"rs904715579","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545215,"feature_type":"variation","strand":1,"end":140545215,"alleles":["C","T"]},{"start":140545217,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140545217,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1321868729","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545218,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140545218,"clinical_significance":[],"seq_region_name":"7","id":"rs1195506167"},{"id":"rs1796847164","seq_region_name":"7","clinical_significance":[],"end":140545220,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140545220,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140545226,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545226,"source":"dbSNP","id":"rs1000278757","seq_region_name":"7","clinical_significance":[]},{"start":140545227,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140545227,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1053785833","clinical_significance":[]},{"alleles":["C","A"],"end":140545228,"strand":1,"feature_type":"variation","start":140545228,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1371545638","clinical_significance":[]},{"clinical_significance":[],"id":"rs962747570","seq_region_name":"7","source":"dbSNP","start":140545232,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140545232,"alleles":["G","A","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1411836401","source":"dbSNP","start":140545236,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140545236,"alleles":["G","A","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796847765","alleles":["G","-"],"end":140545240,"feature_type":"variation","strand":1,"source":"dbSNP","start":140545240,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs183585876","end":140545251,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140545251,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140545252,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140545252,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs140201238","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796848231","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545256,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140545256},{"clinical_significance":[],"id":"rs146973038","seq_region_name":"7","source":"dbSNP","start":140545259,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140545259,"alleles":["C","T"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545260,"source":"dbSNP","strand":1,"feature_type":"variation","end":140545260,"alleles":["G","A"],"seq_region_name":"7","id":"rs1163235700","clinical_significance":[]},{"clinical_significance":[],"id":"rs572379987","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545272,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140545272},{"start":140545276,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140545276,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1468119035","clinical_significance":[]},{"id":"rs1175630774","seq_region_name":"7","clinical_significance":[],"start":140545277,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140545277,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs537983972","alleles":["TTTTTT","TTTTT","TTTTTTT"],"end":140545285,"feature_type":"variation","strand":1,"source":"dbSNP","start":140545280,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140545282,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140545282,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130524697","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140545285,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545285,"source":"dbSNP","seq_region_name":"7","id":"rs1247974503","clinical_significance":[]},{"clinical_significance":[],"id":"rs1796849260","seq_region_name":"7","alleles":["G","A"],"end":140545288,"feature_type":"variation","strand":1,"source":"dbSNP","start":140545288,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545292,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140545292,"clinical_significance":[],"id":"rs1194914267","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1488493159","seq_region_name":"7","end":140545293,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140545293,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","T"],"end":140545294,"feature_type":"variation","strand":1,"source":"dbSNP","start":140545294,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1796849598","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1001300416","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140545299,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545299,"source":"dbSNP"},{"alleles":["C","A"],"end":140545304,"feature_type":"variation","strand":1,"source":"dbSNP","start":140545304,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1016670252","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1796850485","clinical_significance":[],"start":140545307,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140545307,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1796850610","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545319,"source":"dbSNP","strand":1,"feature_type":"variation","end":140545319,"alleles":["A","G"]},{"start":140545320,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140545328,"alleles":["TGATATGTG","TG"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1231307380","clinical_significance":[]},{"source":"dbSNP","start":140545322,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140545322,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1334085635"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140545325,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545325,"source":"dbSNP","id":"rs962539213","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1229995186","seq_region_name":"7","alleles":["C","T"],"end":140545333,"feature_type":"variation","strand":1,"source":"dbSNP","start":140545333,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140545334,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140545334,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585594701","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs972528142","alleles":["G","A"],"end":140545341,"feature_type":"variation","strand":1,"source":"dbSNP","start":140545341,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545348,"feature_type":"variation","strand":1,"end":140545348,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs918534227"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545349,"feature_type":"variation","strand":1,"end":140545349,"alleles":["T","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130524827"},{"end":140545352,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140545352,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796852843","clinical_significance":[]},{"id":"rs1796852943","seq_region_name":"7","clinical_significance":[],"end":140545353,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140545353,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545354,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140545354,"seq_region_name":"7","id":"rs955298547","clinical_significance":[]},{"start":140545356,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140545356,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs914769778","clinical_significance":[]},{"alleles":["TCTTCTT","TCTT"],"end":140545363,"strand":1,"feature_type":"variation","start":140545357,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1796853391","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1284273361","clinical_significance":[],"start":140545358,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140545358,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["TTTTTTT","TTTTTT","TTTTTTTT"],"end":140545368,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545362,"source":"dbSNP","id":"rs1323980857","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796853962","clinical_significance":[],"strand":1,"feature_type":"variation","end":140545367,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545367,"source":"dbSNP"},{"id":"rs2130524910","seq_region_name":"7","clinical_significance":[],"alleles":["T","G"],"end":140545368,"strand":1,"feature_type":"variation","start":140545368,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140545372,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140545372,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1461329816"},{"clinical_significance":[],"id":"rs946382845","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545373,"feature_type":"variation","strand":1,"end":140545373,"alleles":["T","C"]},{"end":140545376,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140545376,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796854361","clinical_significance":[]},{"alleles":["C","T"],"end":140545383,"strand":1,"feature_type":"variation","start":140545383,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs987904139","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs911910224","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545386,"feature_type":"variation","strand":1,"end":140545386,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1363636011","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545387,"feature_type":"variation","strand":1,"end":140545387,"alleles":["G","C"]},{"start":140545389,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140545389,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130524973","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs943349625","source":"dbSNP","start":140545390,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140545390,"alleles":["G","A"],"feature_type":"variation","strand":1},{"alleles":["C","T"],"end":140545393,"feature_type":"variation","strand":1,"source":"dbSNP","start":140545393,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs772213319"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545395,"feature_type":"variation","strand":1,"end":140545395,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1796855282"},{"clinical_significance":[],"id":"rs926003849","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140545401,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545401},{"clinical_significance":[],"seq_region_name":"7","id":"rs939081338","source":"dbSNP","start":140545402,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140545402,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1056735464","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140545405,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545405},{"id":"rs1796855732","seq_region_name":"7","clinical_significance":[],"start":140545413,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140545413,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs775755558","seq_region_name":"7","feature_type":"variation","strand":1,"end":140545423,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545423},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545429,"feature_type":"variation","strand":1,"end":140545429,"alleles":["C","T"],"clinical_significance":[],"id":"rs1330500199","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140545431,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545431,"clinical_significance":[],"id":"rs1796856077","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1773496955","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140545432,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545432},{"end":140545433,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140545433,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796856176"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545434,"feature_type":"variation","strand":1,"end":140545434,"alleles":["T","C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs138151721"},{"end":140545436,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140545436,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs747076373","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140545437,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545437,"clinical_significance":[],"seq_region_name":"7","id":"rs1278774106"},{"seq_region_name":"7","id":"rs779415791","clinical_significance":[],"strand":1,"feature_type":"variation","end":140545446,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545446,"source":"dbSNP"},{"end":140545448,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140545448,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796856745","clinical_significance":[]},{"start":140545453,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140545453,"strand":1,"feature_type":"variation","id":"rs892067257","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140545454,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545454,"source":"dbSNP","seq_region_name":"7","id":"rs1014497662","clinical_significance":[]},{"source":"dbSNP","start":140545463,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140545463,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796856943"},{"alleles":["G","A"],"end":140545469,"strand":1,"feature_type":"variation","start":140545469,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1796857061","seq_region_name":"7","clinical_significance":[]},{"end":140545471,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140545471,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1259795197"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545471,"feature_type":"variation","strand":1,"alleles":["TT","T"],"end":140545472,"clinical_significance":[],"seq_region_name":"7","id":"rs1796857285"},{"seq_region_name":"7","id":"rs1796857409","clinical_significance":[],"start":140545473,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140545473,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"end":140545477,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140545477,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs2130525204","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1440257772","end":140545478,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140545478,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140545481,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140545481,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1796857652","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1389523889","end":140545486,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140545486,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140545488,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140545488,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1323115122"},{"alleles":["G","C"],"end":140545493,"strand":1,"feature_type":"variation","start":140545493,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1446595386","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545499,"feature_type":"variation","strand":1,"end":140545499,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1384618112"},{"feature_type":"variation","strand":1,"end":140545500,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545500,"clinical_significance":[],"seq_region_name":"7","id":"rs370636381"},{"alleles":["C","T"],"end":140545504,"feature_type":"variation","strand":1,"source":"dbSNP","start":140545504,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs748725222"},{"seq_region_name":"7","id":"rs1479241185","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545507,"source":"dbSNP","strand":1,"feature_type":"variation","end":140545507,"alleles":["T","C"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545508,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140545508,"seq_region_name":"7","id":"rs1585595038","clinical_significance":[]},{"end":140545509,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140545509,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1396499312"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545512,"feature_type":"variation","strand":1,"end":140545512,"alleles":["G","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs772687548"},{"seq_region_name":"7","id":"rs1796859139","clinical_significance":[],"alleles":["C","A"],"end":140545514,"strand":1,"feature_type":"variation","start":140545514,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1796859251","clinical_significance":[],"end":140545516,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140545516,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1796859341","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545517,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140545517},{"end":140545520,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140545520,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796859449","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796859570","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545523,"source":"dbSNP","strand":1,"feature_type":"variation","end":140545523,"alleles":["G","A"]},{"alleles":["A","G"],"end":140545525,"strand":1,"feature_type":"variation","start":140545525,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs905545798","clinical_significance":[]},{"seq_region_name":"7","id":"rs1001162809","clinical_significance":[],"start":140545528,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140545528,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1248126113","feature_type":"variation","strand":1,"end":140545532,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545532},{"seq_region_name":"7","id":"rs1796860016","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545541,"source":"dbSNP","strand":1,"feature_type":"variation","end":140545543,"alleles":["GGG","GG"]},{"alleles":["G","C","T"],"end":140545542,"feature_type":"variation","strand":1,"source":"dbSNP","start":140545542,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1190393347"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796860266","end":140545543,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140545543,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1479334357","end":140545544,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140545544,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1796860477","seq_region_name":"7","source":"dbSNP","start":140545546,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140545546,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545547,"source":"dbSNP","strand":1,"feature_type":"variation","end":140545547,"alleles":["C","T"],"seq_region_name":"7","id":"rs188273886","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545550,"source":"dbSNP","strand":1,"feature_type":"variation","end":140545550,"alleles":["C","T"],"seq_region_name":"7","id":"rs1283227638","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545552,"source":"dbSNP","strand":1,"feature_type":"variation","end":140545552,"alleles":["T","A","C"],"seq_region_name":"7","id":"rs962446285","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545558,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140545558,"clinical_significance":[],"seq_region_name":"7","id":"rs1796860936"},{"source":"dbSNP","start":140545559,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140545559,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1796861079","seq_region_name":"7"},{"end":140545561,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140545561,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796861198"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140545566,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545566,"source":"dbSNP","id":"rs898391538","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796861432","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545569,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140545569},{"seq_region_name":"7","id":"rs994024011","clinical_significance":[],"alleles":["C","G","T"],"end":140545570,"strand":1,"feature_type":"variation","start":140545570,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140545571,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140545571,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1025461988","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1365963235","feature_type":"variation","strand":1,"end":140545575,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545575},{"source":"dbSNP","start":140545577,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140545577,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs564765416"},{"seq_region_name":"7","id":"rs1796862130","clinical_significance":[],"start":140545584,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140545584,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140545587,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545587,"clinical_significance":[],"seq_region_name":"7","id":"rs955354829"},{"seq_region_name":"7","id":"rs1025579082","clinical_significance":[],"end":140545592,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140545592,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1429165952","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545593,"feature_type":"variation","strand":1,"end":140545593,"alleles":["C","T"]},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140545594,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545594,"clinical_significance":[],"id":"rs1585595251","seq_region_name":"7"},{"source":"dbSNP","start":140545595,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140545595,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs531795939"},{"id":"rs1796863125","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545596,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140545596},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545597,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140545597,"seq_region_name":"7","id":"rs1796863250","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140545600,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545600,"source":"dbSNP","seq_region_name":"7","id":"rs1796863368","clinical_significance":[]},{"seq_region_name":"7","id":"rs549915023","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140545602,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545602,"source":"dbSNP"},{"source":"dbSNP","start":140545603,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140545603,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs911088695","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1171303275","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545608,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140545608},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796863906","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545613,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140545613},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585595289","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545614,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140545614},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545620,"source":"dbSNP","strand":1,"feature_type":"variation","end":140545620,"alleles":["G","A"],"id":"rs1796864148","seq_region_name":"7","clinical_significance":[]},{"end":140545632,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140545632,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs762900460","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796864411","clinical_significance":[],"strand":1,"feature_type":"variation","end":140545637,"alleles":["TGGG","TGGGTGGG"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545634,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1405532496","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545637,"source":"dbSNP","strand":1,"feature_type":"variation","end":140545637,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1304588448","source":"dbSNP","start":140545639,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140545639,"alleles":["T","G"],"feature_type":"variation","strand":1},{"id":"rs1796864820","seq_region_name":"7","clinical_significance":[],"start":140545642,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140545642,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585595338","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545646,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140545646},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796865049","source":"dbSNP","start":140545647,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140545647,"feature_type":"variation","strand":1},{"end":140545656,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140545656,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs974705244","clinical_significance":[]},{"alleles":["G","A","T"],"end":140545657,"feature_type":"variation","strand":1,"source":"dbSNP","start":140545657,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs926077412"},{"end":140545660,"alleles":["GTGT","GTGTGTGT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140545657,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796865428"},{"seq_region_name":"7","id":"rs1796865556","clinical_significance":[],"start":140545658,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140545657,"alleles":["-","CACTCGGCACTTTGATTGTTTC"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1403481037","source":"dbSNP","start":140545658,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140545658,"alleles":["T","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796865777","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140545659,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545659},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585595371","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545661,"feature_type":"variation","strand":1,"end":140545661,"alleles":["A","C"]},{"feature_type":"variation","strand":1,"end":140545663,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545663,"clinical_significance":[],"seq_region_name":"7","id":"rs1796866018"},{"source":"dbSNP","start":140545666,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140545666,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs147227934"},{"seq_region_name":"7","id":"rs547984573","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545669,"source":"dbSNP","strand":1,"feature_type":"variation","end":140545669,"alleles":["T","G"]},{"end":140545670,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140545670,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1241851628","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585595431","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545674,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140545674},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545676,"feature_type":"variation","strand":1,"end":140545676,"alleles":["A","C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1796866776"},{"clinical_significance":[],"seq_region_name":"7","id":"rs193172978","source":"dbSNP","start":140545677,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140545677,"alleles":["T","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs373317841","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545683,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140545683},{"seq_region_name":"7","id":"rs1796867097","clinical_significance":[],"start":140545690,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140545690,"strand":1,"feature_type":"variation"},{"id":"rs1796867218","seq_region_name":"7","clinical_significance":[],"end":140545694,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140545694,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140545698,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545698,"clinical_significance":[],"id":"rs1796867334","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1188213256","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545700,"source":"dbSNP","strand":1,"feature_type":"variation","end":140545700,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1796867524","clinical_significance":[],"alleles":["T","C"],"end":140545704,"strand":1,"feature_type":"variation","start":140545704,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140545705,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545705,"source":"dbSNP","seq_region_name":"7","id":"rs1443910410","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545706,"feature_type":"variation","strand":1,"end":140545706,"alleles":["T","A","C"],"clinical_significance":[],"id":"rs1585595478","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1350057133","clinical_significance":[],"start":140545710,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","TT"],"end":140545710,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1563130094","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140545720,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545720},{"seq_region_name":"7","id":"rs913416271","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545723,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140545723},{"seq_region_name":"7","id":"rs1210588328","clinical_significance":[],"alleles":["C","A"],"end":140545730,"strand":1,"feature_type":"variation","start":140545730,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796868339","source":"dbSNP","start":140545731,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140545731,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1343156958","alleles":["A","C"],"end":140545739,"feature_type":"variation","strand":1,"source":"dbSNP","start":140545739,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["TTTTTTT","TTTTTT","TTTTTTTT"],"end":140545748,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545742,"clinical_significance":[],"seq_region_name":"7","id":"rs1277105205"},{"seq_region_name":"7","id":"rs1796868674","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140545744,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545744,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140545748,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545748,"source":"dbSNP","seq_region_name":"7","id":"rs1212873895","clinical_significance":[]},{"id":"rs1294208918","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545751,"source":"dbSNP","strand":1,"feature_type":"variation","end":140545751,"alleles":["C","G"]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140545752,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545752,"clinical_significance":[],"seq_region_name":"7","id":"rs1338866634"},{"seq_region_name":"7","id":"rs766241493","clinical_significance":[],"alleles":["T","A"],"end":140545754,"strand":1,"feature_type":"variation","start":140545754,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140545757,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545757,"source":"dbSNP","seq_region_name":"7","id":"rs1796869220","clinical_significance":[]},{"source":"dbSNP","start":140545758,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C","G"],"end":140545758,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs938966643"},{"start":140545762,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140545762,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs1796869499","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545763,"feature_type":"variation","strand":1,"end":140545763,"alleles":["G","A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs76501224"},{"end":140545768,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140545768,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs906080679","clinical_significance":[]},{"start":140545769,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140545769,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1413729809","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140545771,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545771,"clinical_significance":[],"seq_region_name":"7","id":"rs894866338"},{"strand":1,"feature_type":"variation","end":140545773,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545773,"source":"dbSNP","id":"rs185402805","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1163721612","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545774,"source":"dbSNP","strand":1,"feature_type":"variation","end":140545774,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1476165061","clinical_significance":[],"end":140545775,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140545775,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140545777,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545777,"clinical_significance":[],"id":"rs1415319060","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1038595584","end":140545779,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140545779,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1179591281","source":"dbSNP","start":140545780,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140545780,"alleles":["C","A"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140545783,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545783,"clinical_significance":[],"seq_region_name":"7","id":"rs1483298476"},{"end":140545786,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140545786,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1038040767","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545787,"source":"dbSNP","strand":1,"feature_type":"variation","end":140545787,"alleles":["T","A","C"],"seq_region_name":"7","id":"rs1202750498","clinical_significance":[]},{"end":140545788,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140545788,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796872405"},{"source":"dbSNP","start":140545795,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140545795,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs898438965"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796872909","end":140545796,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140545796,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545797,"feature_type":"variation","strand":1,"end":140545797,"alleles":["T","A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs752450254"},{"start":140545798,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G","T"],"end":140545798,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1363310815","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs993943985","alleles":["T","C","G"],"end":140545805,"feature_type":"variation","strand":1,"source":"dbSNP","start":140545805,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1585595790","seq_region_name":"7","clinical_significance":[],"end":140545809,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140545809,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140545811,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140545811,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1025791342"},{"end":140545812,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140545812,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs117484733","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1796874522","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140545823,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545823},{"seq_region_name":"7","id":"rs2130526239","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545827,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140545827},{"seq_region_name":"7","id":"rs553240447","clinical_significance":[],"start":140545828,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140545828,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1008440366","source":"dbSNP","start":140545829,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140545829,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs114841748","feature_type":"variation","strand":1,"end":140545830,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545830},{"feature_type":"variation","strand":1,"end":140545835,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545835,"clinical_significance":[],"seq_region_name":"7","id":"rs1796875321"},{"seq_region_name":"7","id":"rs1796875505","clinical_significance":[],"strand":1,"feature_type":"variation","end":140545836,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545836,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545837,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140545837,"id":"rs115718863","seq_region_name":"7","clinical_significance":[]},{"id":"rs1796875933","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140545843,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545843,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1796876101","clinical_significance":[],"strand":1,"feature_type":"variation","end":140545846,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545846,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1585595878","clinical_significance":[],"end":140545847,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140545847,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs974739661","clinical_significance":[],"end":140545848,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140545848,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1585595902","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140545851,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545851,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545852,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140545852,"clinical_significance":[],"id":"rs1246786037","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140545858,"alleles":["CCTCCCT","CCTCCCTCCCT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545852,"source":"dbSNP","seq_region_name":"7","id":"rs2130526366","clinical_significance":[]},{"clinical_significance":[],"id":"rs1585595931","seq_region_name":"7","end":140545854,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140545854,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140545856,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545856,"source":"dbSNP","seq_region_name":"7","id":"rs1796877196","clinical_significance":[]},{"end":140545860,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140545860,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796877391"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1323652594","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545862,"feature_type":"variation","strand":1,"end":140545864,"alleles":["ACA","A"]},{"seq_region_name":"7","id":"rs1462612817","clinical_significance":[],"end":140545865,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","start":140545865,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1392196707","end":140545866,"alleles":["C","A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140545866,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140545867,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140545867,"alleles":["C","A","G"],"strand":1,"feature_type":"variation","id":"rs1018378142","seq_region_name":"7","clinical_significance":[]},{"start":140545870,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140545870,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796878453","clinical_significance":[]},{"start":140545871,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140545871,"alleles":["T","C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1032963208","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140545873,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545873,"clinical_significance":[],"seq_region_name":"7","id":"rs1796878846"},{"seq_region_name":"7","id":"rs1796879046","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140545874,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545874,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140545875,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545875,"source":"dbSNP","id":"rs1585595995","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545882,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140545882,"clinical_significance":[],"seq_region_name":"7","id":"rs190650717"},{"start":140545887,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140545887,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs568255291","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796879816","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140545890,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545890,"source":"dbSNP"},{"seq_region_name":"7","id":"rs2130526517","clinical_significance":[],"start":140545893,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140545893,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140545896,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140545896,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs988931898"},{"clinical_significance":[],"seq_region_name":"7","id":"rs763654553","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545900,"feature_type":"variation","strand":1,"end":140545900,"alleles":["G","A"]},{"source":"dbSNP","start":140545909,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140545909,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs145404228"},{"end":140545911,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140545911,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1251616550","clinical_significance":[]},{"clinical_significance":[],"id":"rs1796880838","seq_region_name":"7","end":140545912,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140545912,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1481495746","seq_region_name":"7","feature_type":"variation","strand":1,"end":140545914,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545914},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545916,"source":"dbSNP","strand":1,"feature_type":"variation","end":140545916,"alleles":["G","C"],"seq_region_name":"7","id":"rs146234092","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545919,"source":"dbSNP","strand":1,"feature_type":"variation","end":140545923,"alleles":["ACACA","ACA"],"id":"rs1796881451","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130526603","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545920,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140545920},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796881685","end":140545923,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140545923,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545924,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140545924,"clinical_significance":[],"seq_region_name":"7","id":"rs1796881880"},{"alleles":["ATTGCTGTT","-"],"end":140545935,"strand":1,"feature_type":"variation","start":140545927,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796882067","clinical_significance":[]},{"seq_region_name":"7","id":"rs967658352","clinical_significance":[],"end":140545930,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140545930,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545931,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140545931,"seq_region_name":"7","id":"rs1796882443","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140545934,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545934,"source":"dbSNP","seq_region_name":"7","id":"rs927571526","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796882774","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140545935,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545935},{"feature_type":"variation","strand":1,"end":140545942,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545942,"clinical_significance":[],"id":"rs937562907","seq_region_name":"7"},{"source":"dbSNP","start":140545943,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140545943,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130526676"},{"alleles":["G","T"],"end":140545945,"feature_type":"variation","strand":1,"source":"dbSNP","start":140545945,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs572362532"},{"alleles":["G","A"],"end":140545946,"feature_type":"variation","strand":1,"source":"dbSNP","start":140545946,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796883151"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796883278","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545947,"feature_type":"variation","strand":1,"end":140545947,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796883388","feature_type":"variation","strand":1,"end":140545950,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545950},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545953,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140545953,"clinical_significance":[],"seq_region_name":"7","id":"rs898182320"},{"strand":1,"feature_type":"variation","end":140545954,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545954,"source":"dbSNP","id":"rs1796883533","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1796883679","seq_region_name":"7","end":140545955,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140545955,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140545957,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140545957,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796883808"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545958,"feature_type":"variation","strand":1,"end":140545958,"alleles":["G","T"],"clinical_significance":[],"id":"rs1796883949","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1305352585","end":140545963,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140545963,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs2130526773","seq_region_name":"7","feature_type":"variation","strand":1,"end":140545964,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545964},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545968,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140545968,"clinical_significance":[],"seq_region_name":"7","id":"rs1221653168"},{"seq_region_name":"7","id":"rs1372139428","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545973,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140545973},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140545974,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140545974,"source":"dbSNP","seq_region_name":"7","id":"rs1275140992","clinical_significance":[]},{"start":140545975,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140545975,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796884555","clinical_significance":[]},{"clinical_significance":[],"id":"rs1585596169","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545979,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140545979},{"start":140545980,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140545980,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1184873753","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140545982,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545982,"clinical_significance":[],"seq_region_name":"7","id":"rs1585596196"},{"clinical_significance":[],"id":"rs1796885072","seq_region_name":"7","end":140545988,"alleles":["CTCCTCC","CTCC"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140545982,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs376757112","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140545984,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545984},{"source":"dbSNP","start":140545985,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140545985,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796885324"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796885463","feature_type":"variation","strand":1,"end":140545989,"alleles":["CCC","CC"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545987},{"end":140545989,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140545989,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1796885646","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1391711345","seq_region_name":"7","feature_type":"variation","strand":1,"end":140545991,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140545991},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796885973","end":140545994,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140545994,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140545996,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140545996,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796886149"},{"clinical_significance":[],"id":"rs188456236","seq_region_name":"7","feature_type":"variation","strand":1,"end":140546005,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546005},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546006,"source":"dbSNP","strand":1,"feature_type":"variation","end":140546006,"alleles":["G","T"],"seq_region_name":"7","id":"rs1796886535","clinical_significance":[]},{"start":140546011,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140546011,"alleles":["C","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796886720","clinical_significance":[]},{"start":140546012,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140546012,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1457727411","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796887083","clinical_significance":[],"alleles":["C","T"],"end":140546019,"strand":1,"feature_type":"variation","start":140546019,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["A","C"],"end":140546022,"feature_type":"variation","strand":1,"source":"dbSNP","start":140546022,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130526940"},{"seq_region_name":"7","id":"rs1443585068","clinical_significance":[],"start":140546024,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140546024,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140546025,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546025,"clinical_significance":[],"seq_region_name":"7","id":"rs1796887448"},{"seq_region_name":"7","id":"rs1046817148","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140546026,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546026,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1346672820","end":140546037,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140546037,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140546039,"alleles":["AA","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546038,"clinical_significance":[],"seq_region_name":"7","id":"rs1156680793"},{"clinical_significance":[],"seq_region_name":"7","id":"rs960380965","source":"dbSNP","start":140546044,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140546044,"feature_type":"variation","strand":1},{"alleles":["A","T"],"end":140546052,"feature_type":"variation","strand":1,"source":"dbSNP","start":140546052,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1796888448","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546056,"source":"dbSNP","strand":1,"feature_type":"variation","end":140546056,"alleles":["G","T"],"seq_region_name":"7","id":"rs1796888614","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1426134288","feature_type":"variation","strand":1,"end":140546058,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546058},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796888855","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140546059,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546059},{"seq_region_name":"7","id":"rs1796889002","clinical_significance":[],"start":140546061,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140546061,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs558219054","end":140546068,"alleles":["CTTCTTCT","CTTCT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140546061,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs867958248","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140546062,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546062,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1452637186","end":140546065,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140546065,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546067,"source":"dbSNP","strand":1,"feature_type":"variation","end":140546067,"alleles":["C","T"],"seq_region_name":"7","id":"rs890859899","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130527086","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546071,"source":"dbSNP","strand":1,"feature_type":"variation","end":140546071,"alleles":["T","G"]},{"end":140546072,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140546072,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs2130527096","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140546073,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546073,"source":"dbSNP","seq_region_name":"7","id":"rs1796889589","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546078,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140546078,"clinical_significance":[],"seq_region_name":"7","id":"rs1563130314"},{"seq_region_name":"7","id":"rs1796889805","clinical_significance":[],"end":140546084,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140546084,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1189730836","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546086,"source":"dbSNP","strand":1,"feature_type":"variation","end":140546086,"alleles":["G","A"]},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140546087,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546087,"clinical_significance":[],"id":"rs1796890024","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1796890139","clinical_significance":[],"alleles":["G","A"],"end":140546091,"strand":1,"feature_type":"variation","start":140546091,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1008099614","seq_region_name":"7","clinical_significance":[],"end":140546092,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140546092,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs2130527157","seq_region_name":"7","alleles":["G","A"],"end":140546093,"feature_type":"variation","strand":1,"source":"dbSNP","start":140546093,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140546096,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140546096,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796890246"},{"id":"rs2130527167","seq_region_name":"7","clinical_significance":[],"start":140546097,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140546097,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140546099,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546099,"source":"dbSNP","seq_region_name":"7","id":"rs2130527176","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130527188","clinical_significance":[],"start":140546100,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140546100,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"alleles":["G","A"],"end":140546101,"strand":1,"feature_type":"variation","start":140546101,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs568435105","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130527200","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546103,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140546103},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546104,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140546104,"clinical_significance":[],"seq_region_name":"7","id":"rs138653549"},{"start":140546105,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140546105,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796890605","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546106,"source":"dbSNP","strand":1,"feature_type":"variation","end":140546106,"alleles":["G","A"],"seq_region_name":"7","id":"rs1796890723","clinical_significance":[]},{"id":"rs1796890855","seq_region_name":"7","clinical_significance":[],"start":140546108,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140546108,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140546109,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546109,"clinical_significance":[],"seq_region_name":"7","id":"rs576374196"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1215514166","alleles":["C","T"],"end":140546111,"feature_type":"variation","strand":1,"source":"dbSNP","start":140546111,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546121,"source":"dbSNP","strand":1,"feature_type":"variation","end":140546121,"alleles":["C","T"],"id":"rs181091573","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796891642","source":"dbSNP","start":140546128,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A","C"],"end":140546128,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140546130,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140546130,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1796891863","seq_region_name":"7"},{"id":"rs2130527283","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140546137,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546137,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546141,"feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140546141,"clinical_significance":[],"seq_region_name":"7","id":"rs750794775"},{"clinical_significance":[],"seq_region_name":"7","id":"rs561978025","source":"dbSNP","start":140546145,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140546145,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs758818323","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546146,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140546146},{"alleles":["C","A","T"],"end":140546147,"strand":1,"feature_type":"variation","start":140546147,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs769685209","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546148,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140546148,"clinical_significance":[],"id":"rs989185182","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs529425291","source":"dbSNP","start":140546152,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140546152,"alleles":["G","A","C","T"],"feature_type":"variation","strand":1},{"end":140546155,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140546155,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130527384","clinical_significance":[]},{"id":"rs1020402202","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140546156,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546156,"source":"dbSNP"},{"start":140546157,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140546157,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs971886591","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs981658150","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140546158,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546158},{"strand":1,"feature_type":"variation","end":140546159,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546159,"source":"dbSNP","seq_region_name":"7","id":"rs2130527424","clinical_significance":[]},{"start":140546162,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140546162,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1224941541","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140546167,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546167,"clinical_significance":[],"seq_region_name":"7","id":"rs1796894091"},{"clinical_significance":[],"id":"rs374572962","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546169,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140546169},{"clinical_significance":[],"seq_region_name":"7","id":"rs1433128319","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546172,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140546172},{"source":"dbSNP","start":140546173,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140546173,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796894655"},{"alleles":["T","A","G"],"end":140546177,"feature_type":"variation","strand":1,"source":"dbSNP","start":140546177,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs780233438","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1394487896","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546178,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140546178},{"end":140546190,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140546190,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1008241840","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546191,"feature_type":"variation","strand":1,"end":140546191,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1260218504"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546191,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GGG","GG"],"end":140546193,"seq_region_name":"7","id":"rs1430444376","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546193,"source":"dbSNP","strand":1,"feature_type":"variation","end":140546193,"alleles":["G","A"],"seq_region_name":"7","id":"rs1796895812","clinical_significance":[]},{"start":140546194,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140546194,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs888229345","clinical_significance":[]},{"alleles":["A","G"],"end":140546197,"feature_type":"variation","strand":1,"source":"dbSNP","start":140546197,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796896202"},{"start":140546199,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140546199,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796896367","clinical_significance":[]},{"end":140546206,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140546206,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1040096834","seq_region_name":"7","clinical_significance":[]},{"end":140546207,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140546207,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs747270779","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1796896890","seq_region_name":"7","source":"dbSNP","start":140546223,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140546223,"alleles":["T","C","G"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546224,"source":"dbSNP","strand":1,"feature_type":"variation","end":140546224,"alleles":["C","A"],"seq_region_name":"7","id":"rs1796897134","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546228,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140546228,"clinical_significance":[],"seq_region_name":"7","id":"rs1461683812"},{"start":140546231,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AACATGGTGAAAC","AAC"],"end":140546243,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1260086896","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546232,"source":"dbSNP","strand":1,"feature_type":"variation","end":140546232,"alleles":["A","C"],"seq_region_name":"7","id":"rs1205512288","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546242,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140546242,"id":"rs1796897910","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140546244,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546244,"source":"dbSNP","seq_region_name":"7","id":"rs927457774","clinical_significance":[]},{"source":"dbSNP","start":140546246,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140546246,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs775240395","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546247,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140546247,"id":"rs974324614","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546249,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140546249,"clinical_significance":[],"id":"rs920141542","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1796898926","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140546255,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546255,"source":"dbSNP"},{"seq_region_name":"7","id":"rs899953843","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546256,"source":"dbSNP","strand":1,"feature_type":"variation","end":140546256,"alleles":["A","G"]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140546271,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546271,"clinical_significance":[],"id":"rs1308793220","seq_region_name":"7"},{"seq_region_name":"7","id":"rs929689705","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546274,"source":"dbSNP","strand":1,"feature_type":"variation","end":140546274,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1047165630","source":"dbSNP","start":140546275,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140546275,"alleles":["G","A"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546277,"feature_type":"variation","strand":1,"end":140546277,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1355810075"},{"strand":1,"feature_type":"variation","end":140546279,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546279,"source":"dbSNP","id":"rs1796899764","seq_region_name":"7","clinical_significance":[]},{"start":140546282,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140546282,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1314496967","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140546285,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546285,"clinical_significance":[],"seq_region_name":"7","id":"rs1796900112"},{"start":140546289,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140546289,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs1796900290","seq_region_name":"7","clinical_significance":[]},{"start":140546290,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140546290,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796900477","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140546291,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546291,"clinical_significance":[],"seq_region_name":"7","id":"rs1796900664"},{"id":"rs1796900851","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546293,"source":"dbSNP","strand":1,"feature_type":"variation","end":140546293,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1413103683","end":140546296,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140546296,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["A","G"],"end":140546297,"feature_type":"variation","strand":1,"source":"dbSNP","start":140546297,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs368763464"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140546298,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546298,"clinical_significance":[],"id":"rs1012066971","seq_region_name":"7"},{"end":140546308,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140546308,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1021684870"},{"clinical_significance":[],"id":"rs1371428835","seq_region_name":"7","feature_type":"variation","strand":1,"end":140546318,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546318},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546319,"feature_type":"variation","strand":1,"end":140546319,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1796902072"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140546323,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546323,"source":"dbSNP","seq_region_name":"7","id":"rs967542771","clinical_significance":[]},{"seq_region_name":"7","id":"rs1263389438","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546326,"source":"dbSNP","strand":1,"feature_type":"variation","end":140546326,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1796902632","clinical_significance":[],"strand":1,"feature_type":"variation","end":140546330,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546330,"source":"dbSNP"},{"start":140546331,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140546331,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796902811","clinical_significance":[]},{"source":"dbSNP","start":140546334,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140546334,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1426417705"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796903152","alleles":["G","A","C"],"end":140546337,"feature_type":"variation","strand":1,"source":"dbSNP","start":140546337,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs149342760","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546339,"feature_type":"variation","strand":1,"end":140546339,"alleles":["A","G"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546354,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140546354,"clinical_significance":[],"seq_region_name":"7","id":"rs943773714"},{"clinical_significance":[],"seq_region_name":"7","id":"rs186618719","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546356,"feature_type":"variation","strand":1,"end":140546356,"alleles":["T","C"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546357,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140546357,"clinical_significance":[],"seq_region_name":"7","id":"rs1470561315"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1196071137","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546359,"feature_type":"variation","strand":1,"end":140546359,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs1481302108","clinical_significance":[],"start":140546360,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140546360,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs899697280","feature_type":"variation","strand":1,"end":140546366,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546366},{"end":140546367,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140546367,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs768889479","seq_region_name":"7"},{"source":"dbSNP","start":140546369,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140546369,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1796904894","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs991860524","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546374,"feature_type":"variation","strand":1,"end":140546374,"alleles":["C","A"]},{"seq_region_name":"7","id":"rs1231190356","clinical_significance":[],"start":140546380,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140546380,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546382,"feature_type":"variation","strand":1,"end":140546382,"alleles":["C","T"],"clinical_significance":[],"id":"rs1053638833","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1796905329","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546386,"source":"dbSNP","strand":1,"feature_type":"variation","end":140546386,"alleles":["C","G"]},{"seq_region_name":"7","id":"rs1796905446","clinical_significance":[],"alleles":["C","T"],"end":140546387,"strand":1,"feature_type":"variation","start":140546387,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546389,"source":"dbSNP","strand":1,"feature_type":"variation","end":140546389,"alleles":["G","A"],"seq_region_name":"7","id":"rs1307917394","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546393,"feature_type":"variation","strand":1,"alleles":["GGG","GGGG"],"end":140546395,"clinical_significance":[],"id":"rs34773252","seq_region_name":"7"},{"source":"dbSNP","start":140546396,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140546396,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1451992023"},{"start":140546397,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140546397,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs781276000","clinical_significance":[]},{"alleles":["A","C"],"end":140546400,"feature_type":"variation","strand":1,"source":"dbSNP","start":140546400,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs916228573"},{"seq_region_name":"7","id":"rs1796906249","clinical_significance":[],"start":140546401,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140546401,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546402,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140546402,"clinical_significance":[],"seq_region_name":"7","id":"rs1796906395"},{"source":"dbSNP","start":140546411,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140546411,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1462083359"},{"strand":1,"feature_type":"variation","end":140546412,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546412,"source":"dbSNP","seq_region_name":"7","id":"rs1364313206","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546417,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CAAAAACAAAAACAAAAA","CAAAAACAAAAA","CAAAAACAAAAACAAAAACAAAAA"],"end":140546434,"seq_region_name":"7","id":"rs1397316504","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796906997","feature_type":"variation","strand":1,"alleles":["AAAAA","AAAA"],"end":140546422,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546418},{"seq_region_name":"7","id":"rs1380777832","clinical_significance":[],"alleles":["AAAAA","AAAA"],"end":140546428,"strand":1,"feature_type":"variation","start":140546424,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1475074422","clinical_significance":[],"start":140546425,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140546425,"strand":1,"feature_type":"variation"},{"id":"rs1796907509","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546429,"source":"dbSNP","strand":1,"feature_type":"variation","end":140546429,"alleles":["C","-"]},{"end":140546435,"alleles":["AAAAAA","AAAAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140546430,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1563130520"},{"alleles":["T","C"],"end":140546436,"feature_type":"variation","strand":1,"source":"dbSNP","start":140546436,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs764048831","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1796908042","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140546442,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546442,"source":"dbSNP"},{"alleles":["A","G"],"end":140546443,"strand":1,"feature_type":"variation","start":140546443,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796908218","clinical_significance":[]},{"end":140546443,"alleles":["A","AA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140546443,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796908365"},{"alleles":["T","C"],"end":140546444,"feature_type":"variation","strand":1,"source":"dbSNP","start":140546444,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1413193945","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1182037413","source":"dbSNP","start":140546447,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140546447,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140546450,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140546450,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130528240"},{"end":140546451,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140546451,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs969197908","clinical_significance":[]},{"id":"rs2130528262","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140546455,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546455,"source":"dbSNP"},{"start":140546456,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140546456,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1294527962","clinical_significance":[]},{"id":"rs1796909224","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546457,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140546457},{"clinical_significance":[],"id":"rs892370783","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546458,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140546458},{"end":140546459,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140546459,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1324021928","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1225191817","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546465,"feature_type":"variation","strand":1,"end":140546465,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1010277869","feature_type":"variation","strand":1,"end":140546466,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546466},{"seq_region_name":"7","id":"rs1796909958","clinical_significance":[],"alleles":["A","G"],"end":140546473,"strand":1,"feature_type":"variation","start":140546473,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546474,"feature_type":"variation","strand":1,"end":140546474,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs974235773"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1020686680","end":140546475,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140546475,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1585597161","clinical_significance":[],"strand":1,"feature_type":"variation","end":140546481,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546481,"source":"dbSNP"},{"end":140546482,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140546482,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585597174","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796910932","clinical_significance":[],"end":140546483,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140546483,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1333829860","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546483,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AAAA","AAA"],"end":140546486},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546490,"feature_type":"variation","strand":1,"end":140546490,"alleles":["A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs971392357"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130528412","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546497,"feature_type":"variation","strand":1,"end":140546497,"alleles":["A","G"]},{"start":140546501,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140546501,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs748183218","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546502,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140546502,"seq_region_name":"7","id":"rs527299300","clinical_significance":[]},{"clinical_significance":[],"id":"rs1334189177","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546503,"feature_type":"variation","strand":1,"end":140546503,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs751449052","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546504,"source":"dbSNP","strand":1,"feature_type":"variation","end":140546504,"alleles":["G","A","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130528472","source":"dbSNP","start":140546506,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TATTAAAAGA","TATTAAAAGATATTAAAAGA"],"end":140546515,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs958868625","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546514,"feature_type":"variation","strand":1,"end":140546514,"alleles":["G","T"]},{"end":140546516,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140546516,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796912516","clinical_significance":[]},{"alleles":["A","G"],"end":140546517,"feature_type":"variation","strand":1,"source":"dbSNP","start":140546517,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796912685"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1441693982","alleles":["T","G"],"end":140546518,"feature_type":"variation","strand":1,"source":"dbSNP","start":140546518,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1373353573","source":"dbSNP","start":140546519,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140546519,"alleles":["T","G"],"feature_type":"variation","strand":1},{"alleles":["A","T"],"end":140546520,"feature_type":"variation","strand":1,"source":"dbSNP","start":140546520,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1262016342","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs189828806","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546531,"feature_type":"variation","strand":1,"end":140546531,"alleles":["G","C","T"]},{"feature_type":"variation","strand":1,"end":140546535,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546535,"clinical_significance":[],"seq_region_name":"7","id":"rs78603206"},{"source":"dbSNP","start":140546537,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140546537,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1160669856","seq_region_name":"7"},{"start":140546538,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140546538,"alleles":["T","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796914075","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140546539,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546539,"clinical_significance":[],"seq_region_name":"7","id":"rs1796914269"},{"feature_type":"variation","strand":1,"end":140546543,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546543,"clinical_significance":[],"id":"rs531681926","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140546545,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546545,"clinical_significance":[],"seq_region_name":"7","id":"rs1796914609"},{"seq_region_name":"7","id":"rs1796914797","clinical_significance":[],"end":140546550,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140546550,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs550087640","clinical_significance":[],"start":140546553,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140546553,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"end":140546559,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140546559,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796915176"},{"source":"dbSNP","start":140546560,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140546560,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796915417"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796915603","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546567,"feature_type":"variation","strand":1,"end":140546567,"alleles":["G","A"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546568,"source":"dbSNP","strand":1,"feature_type":"variation","end":140546568,"alleles":["G","A"],"seq_region_name":"7","id":"rs2130528630","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546571,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140546571,"clinical_significance":[],"id":"rs1585597330","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585597339","feature_type":"variation","strand":1,"end":140546572,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546572},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546575,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140546575,"clinical_significance":[],"id":"rs912508766","seq_region_name":"7"},{"alleles":["T","C"],"end":140546580,"strand":1,"feature_type":"variation","start":140546580,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs943950119","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140546580,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","TT"],"end":140546580,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1180704001"},{"seq_region_name":"7","id":"rs1039741552","clinical_significance":[],"alleles":["T","C"],"end":140546585,"strand":1,"feature_type":"variation","start":140546585,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546590,"feature_type":"variation","strand":1,"end":140546590,"alleles":["T","C"],"clinical_significance":[],"id":"rs1585597398","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1191597207","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546591,"feature_type":"variation","strand":1,"end":140546591,"alleles":["A","C"]},{"seq_region_name":"7","id":"rs1796917865","clinical_significance":[],"end":140546592,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140546592,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546601,"feature_type":"variation","strand":1,"end":140546601,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1467985221"},{"end":140546607,"alleles":["G","A","C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140546607,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs920227359"},{"seq_region_name":"7","id":"rs1796918420","clinical_significance":[],"end":140546608,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140546608,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140546610,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140546610,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1796918595","seq_region_name":"7"},{"source":"dbSNP","start":140546612,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140546612,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1284935747"},{"alleles":["G","C"],"end":140546614,"strand":1,"feature_type":"variation","start":140546614,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1796918940","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140546619,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546619,"source":"dbSNP","id":"rs1206666903","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140546626,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546626,"clinical_significance":[],"seq_region_name":"7","id":"rs1262848942"},{"seq_region_name":"7","id":"rs1796919445","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140546627,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546627,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796919661","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546628,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140546628},{"source":"dbSNP","start":140546633,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140546633,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs760822697"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546634,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140546634,"seq_region_name":"7","id":"rs181881940","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796920177","feature_type":"variation","strand":1,"end":140546642,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546642},{"seq_region_name":"7","id":"rs1796920357","clinical_significance":[],"start":140546648,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140546648,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs982496816","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546651,"source":"dbSNP","strand":1,"feature_type":"variation","end":140546651,"alleles":["A","C"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546652,"feature_type":"variation","strand":1,"end":140546652,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130528840"},{"clinical_significance":[],"seq_region_name":"7","id":"rs568281860","source":"dbSNP","start":140546653,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140546653,"alleles":["G","A","C"],"feature_type":"variation","strand":1},{"end":140546665,"alleles":["TGAGTGATCTG","TG"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140546655,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796920696"},{"seq_region_name":"7","id":"rs1796920802","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546657,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140546657},{"start":140546664,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","-"],"end":140546664,"strand":1,"feature_type":"variation","id":"rs1202121134","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1235331328","clinical_significance":[],"alleles":["G","A"],"end":140546665,"strand":1,"feature_type":"variation","start":140546665,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1796921332","clinical_significance":[],"start":140546666,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140546666,"strand":1,"feature_type":"variation"},{"start":140546667,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140546667,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs943696665","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796921675","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546669,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140546669},{"seq_region_name":"7","id":"rs1796921854","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546674,"source":"dbSNP","strand":1,"feature_type":"variation","end":140546674,"alleles":["C","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796922026","source":"dbSNP","start":140546675,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140546675,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1350097557","clinical_significance":[],"alleles":["G","T"],"end":140546679,"strand":1,"feature_type":"variation","start":140546679,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1301350054","source":"dbSNP","start":140546680,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140546680,"feature_type":"variation","strand":1},{"start":140546681,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140546681,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1440739801","clinical_significance":[]},{"seq_region_name":"7","id":"rs1039433271","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140546682,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546682,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs535600847","source":"dbSNP","start":140546695,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140546695,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs920981980","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546697,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140546697},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796923266","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140546703,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546703},{"clinical_significance":[],"id":"rs2130528983","seq_region_name":"7","source":"dbSNP","start":140546703,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140546732,"alleles":["TGGACTGCTCACTGAAAGGCAGCCCCTCTG","TGGACTGCTCACTGAAAGGCAGCCCCTCTGGACTGCTCACTGAAAGGCAGCCCCTCTG"],"feature_type":"variation","strand":1},{"start":140546705,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140546705,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs1796923443","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs535518043","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140546706,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546706,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1469778210","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546710,"feature_type":"variation","strand":1,"end":140546710,"alleles":["C","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546713,"source":"dbSNP","strand":1,"feature_type":"variation","end":140546713,"alleles":["A","G"],"id":"rs1796923984","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130529032","feature_type":"variation","strand":1,"alleles":["T","A"],"end":140546715,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546715},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140546717,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546717,"source":"dbSNP","seq_region_name":"7","id":"rs1585597604","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796924377","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140546718,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546718,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1380858182","feature_type":"variation","strand":1,"alleles":["A","T"],"end":140546719,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546719},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140546720,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546720,"clinical_significance":[],"seq_region_name":"7","id":"rs1796924710"},{"end":140546721,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140546721,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs903241115","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140546725,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546725,"clinical_significance":[],"id":"rs1796924935","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1157632015","clinical_significance":[],"end":140546726,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140546726,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140546728,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140546728,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796925151"},{"alleles":["T","C"],"end":140546729,"strand":1,"feature_type":"variation","start":140546729,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs117506929","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546735,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140546735,"clinical_significance":[],"seq_region_name":"7","id":"rs1396300985"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1053548796","alleles":["C","T"],"end":140546737,"feature_type":"variation","strand":1,"source":"dbSNP","start":140546737,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs892407733","source":"dbSNP","start":140546738,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140546738,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546739,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140546739,"clinical_significance":[],"seq_region_name":"7","id":"rs1796925573"},{"start":140546740,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140546740,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1242597069","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1035845176","end":140546741,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140546741,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140546742,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546742,"source":"dbSNP","seq_region_name":"7","id":"rs2130529196","clinical_significance":[]},{"id":"rs566117222","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140546745,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546745,"source":"dbSNP"},{"alleles":["G","A"],"end":140546746,"feature_type":"variation","strand":1,"source":"dbSNP","start":140546746,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796926007"},{"feature_type":"variation","strand":1,"end":140546747,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546747,"clinical_significance":[],"seq_region_name":"7","id":"rs1796926120"},{"seq_region_name":"7","id":"rs769846311","clinical_significance":[],"start":140546748,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140546748,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs2130529255","clinical_significance":[],"alleles":["G","A"],"end":140546750,"strand":1,"feature_type":"variation","start":140546750,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140546753,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546753,"source":"dbSNP","seq_region_name":"7","id":"rs539547036","clinical_significance":[]},{"id":"rs749535374","seq_region_name":"7","clinical_significance":[],"end":140546754,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140546754,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs768763211","clinical_significance":[],"alleles":["G","C"],"end":140546755,"strand":1,"feature_type":"variation","start":140546755,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1211080414","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546757,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140546757},{"start":140546760,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140546760,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1359662609","clinical_significance":[]},{"start":140546762,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140546762,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs373635101","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1450638068","source":"dbSNP","start":140546763,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140546763,"alleles":["C","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1023180398","clinical_significance":[],"start":140546766,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","T"],"end":140546766,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1233655117","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546771,"source":"dbSNP","strand":1,"feature_type":"variation","end":140546771,"alleles":["G","A","C"]},{"source":"dbSNP","start":140546772,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140546772,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs760568096"},{"seq_region_name":"7","id":"rs1046287006","clinical_significance":[],"end":140546775,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140546775,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140546777,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546777,"source":"dbSNP","seq_region_name":"7","id":"rs1585597867","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546779,"source":"dbSNP","strand":1,"feature_type":"variation","end":140546779,"alleles":["G","A"],"seq_region_name":"7","id":"rs770862327","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796927858","feature_type":"variation","strand":1,"end":140546782,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546782},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546785,"source":"dbSNP","strand":1,"feature_type":"variation","end":140546785,"alleles":["G","A"],"seq_region_name":"7","id":"rs776354243","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796928071","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140546787,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546787},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796928177","end":140546788,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140546788,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["G","T"],"end":140546789,"strand":1,"feature_type":"variation","start":140546789,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1459545463","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140546794,"assembly_name":"GRCh38","consequence_type":"splice_donor_5th_base_variant","start":140546794,"source":"dbSNP","seq_region_name":"7","id":"rs759315002","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"splice_donor_region_variant","start":140546795,"source":"dbSNP","strand":1,"feature_type":"variation","end":140546795,"alleles":["T","C"],"seq_region_name":"7","id":"rs907200005","clinical_significance":[]},{"id":"rs1796928564","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140546796,"strand":1,"feature_type":"variation","start":140546796,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_donor_region_variant"},{"feature_type":"variation","strand":1,"end":140546798,"alleles":["C","T"],"consequence_type":"splice_donor_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546798,"clinical_significance":[],"id":"rs1796928677","seq_region_name":"7"},{"start":140546799,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140546799,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs765009333","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563130790","end":140546800,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140546800,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs775177570","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140546803,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140546803,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140546807,"source":"dbSNP","strand":1,"feature_type":"variation","end":140546807,"alleles":["C","T"],"id":"rs35811666","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140546811,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140546811,"source":"dbSNP","seq_region_name":"7","id":"rs1313108105","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs759385072","source":"dbSNP","start":140546813,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["C","A","G"],"end":140546813,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140546817,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140546817,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs762561728"},{"start":140546823,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","end":140546823,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796929753","clinical_significance":[]},{"alleles":["A","G"],"end":140546833,"strand":1,"feature_type":"variation","start":140546833,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs1796929855","clinical_significance":[]},{"seq_region_name":"7","id":"rs1326146458","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140546834,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140546834},{"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140546844,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140546844,"seq_region_name":"7","id":"rs1563130840","clinical_significance":[]},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546849,"feature_type":"variation","strand":1,"end":140546849,"alleles":["G","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs367621201"},{"seq_region_name":"7","id":"rs1796930335","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140546851,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140546851},{"seq_region_name":"7","id":"rs1563130857","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140546852,"source":"dbSNP","strand":1,"feature_type":"variation","end":140546852,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1287612382","end":140546854,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140546854,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796930707","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546860,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140546860},{"seq_region_name":"7","id":"rs1353793786","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140546862,"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140546862,"source":"dbSNP"},{"end":140546868,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140546868,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","id":"rs1417068919","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs372251662","clinical_significance":[],"start":140546870,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["T","C"],"end":140546870,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796931179","source":"dbSNP","start":140546875,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140546875,"alleles":["C","T"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140546876,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140546876,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1258607097"},{"start":140546882,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140546882,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs201053452","clinical_significance":["uncertain significance"]},{"start":140546885,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["G","A","C"],"end":140546885,"strand":1,"feature_type":"variation","id":"rs751023671","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","T"],"end":140546893,"feature_type":"variation","strand":1,"source":"dbSNP","start":140546893,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1246383011"},{"seq_region_name":"7","id":"rs1796931893","clinical_significance":[],"strand":1,"feature_type":"variation","end":140546895,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140546895,"source":"dbSNP"},{"alleles":["G","T"],"end":140546899,"feature_type":"variation","strand":1,"source":"dbSNP","start":140546899,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796932022"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796932136","source":"dbSNP","start":140546901,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","end":140546901,"alleles":["A","G"],"feature_type":"variation","strand":1},{"alleles":["G","A"],"end":140546903,"strand":1,"feature_type":"variation","start":140546903,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs1263106569","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs576012600","source":"dbSNP","start":140546909,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140546909,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs780318641","seq_region_name":"7","source":"dbSNP","start":140546911,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140546911,"alleles":["C","T"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140546912,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140546912,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs749481616"},{"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140546914,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140546914,"source":"dbSNP","seq_region_name":"7","id":"rs755191369","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"stop_gained","start":140546915,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140546915,"id":"rs368464360","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs772199164","seq_region_name":"7","end":140546918,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140546918,"consequence_type":"synonymous_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140546919,"source":"dbSNP","strand":1,"feature_type":"variation","end":140546919,"alleles":["T","C"],"seq_region_name":"7","id":"rs1796933209","clinical_significance":[]},{"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546925,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140546925,"clinical_significance":[],"id":"rs1796933331","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140546928,"alleles":["C","G","T"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546928,"clinical_significance":[],"seq_region_name":"7","id":"rs776546550"},{"alleles":["T","C"],"end":140546932,"feature_type":"variation","strand":1,"source":"dbSNP","start":140546932,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796933580"},{"seq_region_name":"7","id":"rs1486568776","clinical_significance":[],"start":140546942,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_region_variant","end":140546942,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140546943,"assembly_name":"GRCh38","consequence_type":"splice_region_variant","start":140546943,"source":"dbSNP","seq_region_name":"7","id":"rs745833182","clinical_significance":[]},{"seq_region_name":"7","id":"rs779579970","clinical_significance":[],"end":140546943,"alleles":["C","-"],"strand":1,"feature_type":"variation","start":140546943,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_region_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1462554861","alleles":["A","G"],"end":140546945,"feature_type":"variation","strand":1,"source":"dbSNP","start":140546945,"consequence_type":"splice_region_variant","assembly_name":"GRCh38"},{"alleles":["G","A"],"end":140546946,"strand":1,"feature_type":"variation","start":140546946,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_region_variant","seq_region_name":"7","id":"rs1170777995","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1438426073","source":"dbSNP","start":140546947,"consequence_type":"splice_region_variant","assembly_name":"GRCh38","end":140546947,"alleles":["G","A"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"splice_polypyrimidine_tract_variant","start":140546950,"source":"dbSNP","strand":1,"feature_type":"variation","end":140546950,"alleles":["C","T"],"seq_region_name":"7","id":"rs1275210410","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140546953,"alleles":["A","G"],"consequence_type":"splice_polypyrimidine_tract_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546953,"clinical_significance":[],"seq_region_name":"7","id":"rs1796934367"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796934451","consequence_type":"splice_polypyrimidine_tract_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546956,"feature_type":"variation","strand":1,"end":140546955,"alleles":["-","CTGAGGTG"]},{"seq_region_name":"7","id":"rs543734931","clinical_significance":[],"start":140546957,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140546957,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs75668888","feature_type":"variation","strand":1,"end":140546960,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546960},{"seq_region_name":"7","id":"rs762626132","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140546968,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546968,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140546969,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546969,"clinical_significance":[],"seq_region_name":"7","id":"rs1563131022"},{"seq_region_name":"7","id":"rs763655557","clinical_significance":[],"start":140546971,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140546971,"alleles":["C","G","T"],"strand":1,"feature_type":"variation"},{"alleles":["C","G","T"],"end":140546972,"strand":1,"feature_type":"variation","start":140546972,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs75343023","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140546973,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140546973,"id":"rs369700336","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs983458700","source":"dbSNP","start":140546976,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140546976,"feature_type":"variation","strand":1},{"start":140546977,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","T"],"end":140546977,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1563131044","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546989,"feature_type":"variation","strand":1,"end":140546989,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1339426224"},{"source":"dbSNP","start":140546990,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140546990,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs767198707"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140546992,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140546992,"clinical_significance":[],"seq_region_name":"7","id":"rs943852643"},{"id":"rs1585598437","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547007,"source":"dbSNP","strand":1,"feature_type":"variation","end":140547007,"alleles":["G","A"]},{"end":140547008,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140547008,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs965024543"},{"clinical_significance":[],"seq_region_name":"7","id":"rs975739050","alleles":["G","A","T"],"end":140547009,"feature_type":"variation","strand":1,"source":"dbSNP","start":140547009,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1442762253","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547010,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140547010},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796936287","source":"dbSNP","start":140547012,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140547012,"alleles":["G","A"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547025,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GG","GGG"],"end":140547026,"seq_region_name":"7","id":"rs1354551562","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs144679122","alleles":["T","C","G"],"end":140547027,"feature_type":"variation","strand":1,"source":"dbSNP","start":140547027,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140547031,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547031,"clinical_significance":[],"seq_region_name":"7","id":"rs1371169183"},{"clinical_significance":[],"id":"rs1585598507","seq_region_name":"7","end":140547037,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140547037,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140547041,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140547041,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs947389958"},{"start":140547043,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140547043,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1399453604","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140547048,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547048,"clinical_significance":[],"seq_region_name":"7","id":"rs975041588"},{"clinical_significance":[],"id":"rs1796937139","seq_region_name":"7","feature_type":"variation","strand":1,"end":140547050,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547050},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547052,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140547052,"clinical_significance":[],"seq_region_name":"7","id":"rs2130530217"},{"alleles":["T","C"],"end":140547055,"strand":1,"feature_type":"variation","start":140547055,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1476053770","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140547059,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547059,"clinical_significance":[],"seq_region_name":"7","id":"rs1043066795"},{"end":140547062,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140547062,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1181430467"},{"id":"rs1222686502","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140547063,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547063,"source":"dbSNP"},{"source":"dbSNP","start":140547064,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140547064,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796937699"},{"alleles":["G","A"],"end":140547066,"feature_type":"variation","strand":1,"source":"dbSNP","start":140547066,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796937824"},{"seq_region_name":"7","id":"rs921052477","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140547071,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547071,"source":"dbSNP"},{"clinical_significance":[],"id":"rs551430774","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547074,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140547074},{"clinical_significance":[],"seq_region_name":"7","id":"rs1361105314","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547077,"feature_type":"variation","strand":1,"end":140547077,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs903294378","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547078,"feature_type":"variation","strand":1,"end":140547078,"alleles":["C","T"]},{"feature_type":"variation","strand":1,"end":140547080,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547080,"clinical_significance":[],"seq_region_name":"7","id":"rs1259626079"},{"seq_region_name":"7","id":"rs559996614","clinical_significance":[],"end":140547083,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140547083,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140547087,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547087,"source":"dbSNP","id":"rs1796938580","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs527430980","clinical_significance":[],"end":140547088,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140547088,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140547090,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140547090,"alleles":["A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1272952413"},{"start":140547092,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140547092,"alleles":["A","G"],"strand":1,"feature_type":"variation","id":"rs1227328563","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140547093,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140547093,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs936406520"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547094,"feature_type":"variation","strand":1,"end":140547094,"alleles":["A","G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1879901"},{"strand":1,"feature_type":"variation","alleles":["AT","-"],"end":140547095,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547094,"source":"dbSNP","id":"rs1281000441","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547098,"source":"dbSNP","strand":1,"feature_type":"variation","end":140547098,"alleles":["T","C"],"id":"rs377365913","seq_region_name":"7","clinical_significance":[]},{"end":140547099,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140547099,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796939568","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796939689","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547102,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140547102},{"clinical_significance":[],"id":"rs564107326","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547104,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140547104},{"strand":1,"feature_type":"variation","end":140547105,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547105,"source":"dbSNP","seq_region_name":"7","id":"rs913741697","clinical_significance":[]},{"end":140547106,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140547106,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1326444915"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547107,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140547107,"clinical_significance":[],"seq_region_name":"7","id":"rs1462950221"},{"seq_region_name":"7","id":"rs1391938079","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547110,"source":"dbSNP","strand":1,"feature_type":"variation","end":140547110,"alleles":["C","A","T"]},{"seq_region_name":"7","id":"rs1796940383","clinical_significance":[],"start":140547112,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140547112,"alleles":["T","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1796940484","clinical_significance":[],"end":140547113,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140547113,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140547117,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140547117,"strand":1,"feature_type":"variation","id":"rs1796940582","seq_region_name":"7","clinical_significance":[]},{"id":"rs1796940681","seq_region_name":"7","clinical_significance":[],"start":140547118,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140547118,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs945188773","alleles":["C","T"],"end":140547120,"feature_type":"variation","strand":1,"source":"dbSNP","start":140547120,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1023655971","feature_type":"variation","strand":1,"alleles":["TGTGTGT","TGTGT","TGTGTGTGT"],"end":140547127,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547121},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547131,"feature_type":"variation","strand":1,"end":140547131,"alleles":["C","T"],"clinical_significance":[],"id":"rs1175750394","seq_region_name":"7"},{"source":"dbSNP","start":140547132,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140547132,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796941113"},{"id":"rs1439108914","seq_region_name":"7","clinical_significance":[],"start":140547134,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G","T"],"end":140547134,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547135,"source":"dbSNP","strand":1,"feature_type":"variation","end":140547135,"alleles":["C","T"],"seq_region_name":"7","id":"rs1796941354","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140547138,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547138,"clinical_significance":[],"seq_region_name":"7","id":"rs531302425"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547139,"feature_type":"variation","strand":1,"end":140547139,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1235085001"},{"seq_region_name":"7","id":"rs550112131","clinical_significance":[],"alleles":["T","C"],"end":140547143,"strand":1,"feature_type":"variation","start":140547143,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140547145,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140547145,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs117297669","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140547149,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547149,"clinical_significance":[],"id":"rs906440440","seq_region_name":"7"},{"seq_region_name":"7","id":"rs938703823","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547150,"source":"dbSNP","strand":1,"feature_type":"variation","end":140547150,"alleles":["T","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1385972974","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547153,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140547153},{"seq_region_name":"7","id":"rs1796942239","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547155,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140547155},{"seq_region_name":"7","id":"rs1246697271","clinical_significance":[],"start":140547156,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","G"],"end":140547156,"strand":1,"feature_type":"variation"},{"end":140547158,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140547158,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs76109032","seq_region_name":"7"},{"alleles":["A","T"],"end":140547165,"feature_type":"variation","strand":1,"source":"dbSNP","start":140547165,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs894591563"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1319149742","source":"dbSNP","start":140547166,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140547166,"alleles":["G","A","T"],"feature_type":"variation","strand":1},{"alleles":["G","C"],"end":140547167,"feature_type":"variation","strand":1,"source":"dbSNP","start":140547167,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1285892205","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547170,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140547170,"seq_region_name":"7","id":"rs1796942896","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["AAGT","-"],"end":140547175,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547172,"source":"dbSNP","id":"rs1796943006","seq_region_name":"7","clinical_significance":[]},{"end":140547176,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140547176,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs547615645","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547177,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140547177,"clinical_significance":[],"id":"rs1796943248","seq_region_name":"7"},{"id":"rs367674035","seq_region_name":"7","clinical_significance":[],"start":140547178,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140547178,"alleles":["A","G","T"],"strand":1,"feature_type":"variation"},{"start":140547180,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140547181,"alleles":["TT","-"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796943505","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1352249110","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547183,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140547183},{"source":"dbSNP","start":140547187,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140547187,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1796943736","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547190,"feature_type":"variation","strand":1,"alleles":["-","TAG"],"end":140547189,"clinical_significance":[],"seq_region_name":"7","id":"rs1796943825"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547190,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140547190,"seq_region_name":"7","id":"rs1796943930","clinical_significance":[]},{"id":"rs115256018","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547195,"source":"dbSNP","strand":1,"feature_type":"variation","end":140547195,"alleles":["A","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547196,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140547196,"seq_region_name":"7","id":"rs887277931","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140547200,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547200,"source":"dbSNP","seq_region_name":"7","id":"rs539956304","clinical_significance":[]},{"end":140547206,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140547206,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1412716753"},{"alleles":["G","T"],"end":140547212,"feature_type":"variation","strand":1,"source":"dbSNP","start":140547212,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796944724"},{"source":"dbSNP","start":140547220,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140547220,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs551440285"},{"seq_region_name":"7","id":"rs1796945066","clinical_significance":[],"start":140547221,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140547221,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1292908337","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140547225,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547225},{"source":"dbSNP","start":140547231,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140547231,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796945400"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796945557","source":"dbSNP","start":140547232,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140547232,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1431168879","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547236,"feature_type":"variation","strand":1,"end":140547236,"alleles":["A","G","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547239,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140547239,"clinical_significance":[],"id":"rs1796945956","seq_region_name":"7"},{"seq_region_name":"7","id":"rs2130530942","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140547240,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547240,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547241,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140547241,"seq_region_name":"7","id":"rs1796946126","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140547242,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547242,"source":"dbSNP","seq_region_name":"7","id":"rs1346768136","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs150826306","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547243,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140547243},{"id":"rs1796946478","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547245,"source":"dbSNP","strand":1,"feature_type":"variation","end":140547245,"alleles":["G","A"]},{"clinical_significance":[],"id":"rs1796946596","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140547254,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547254},{"clinical_significance":[],"seq_region_name":"7","id":"rs377338454","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547258,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140547258},{"strand":1,"feature_type":"variation","end":140547259,"alleles":["C","A","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547259,"source":"dbSNP","seq_region_name":"7","id":"rs12540766","clinical_significance":[]},{"end":140547262,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140547262,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs957673729"},{"end":140547264,"alleles":["G","C","T"],"strand":1,"feature_type":"variation","start":140547264,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796947159","clinical_significance":[]},{"alleles":["GGGGG","GGGG"],"end":140547268,"strand":1,"feature_type":"variation","start":140547264,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1452730840","seq_region_name":"7","clinical_significance":[]},{"end":140547265,"alleles":["G","A","C","T"],"strand":1,"feature_type":"variation","start":140547265,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs148523018","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs913615879","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547267,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140547267},{"id":"rs945234972","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547268,"source":"dbSNP","strand":1,"feature_type":"variation","end":140547268,"alleles":["G","A","T"]},{"feature_type":"variation","strand":1,"end":140547269,"alleles":["T","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547269,"clinical_significance":[],"seq_region_name":"7","id":"rs1240753058"},{"source":"dbSNP","start":140547276,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140547276,"alleles":["T","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs574229148"},{"end":140547277,"alleles":["G","C","T"],"strand":1,"feature_type":"variation","start":140547277,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs978799221","clinical_significance":[]},{"alleles":["T","A"],"end":140547281,"strand":1,"feature_type":"variation","start":140547281,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1280678739","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs981962356","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140547286,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547286,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1309981191","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547289,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140547289},{"id":"rs1300443522","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140547292,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547292,"source":"dbSNP"},{"source":"dbSNP","start":140547293,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140547293,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796948518"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796948631","source":"dbSNP","start":140547294,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140547294,"alleles":["A","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs535005283","end":140547307,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140547307,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547309,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140547309,"clinical_significance":[],"seq_region_name":"7","id":"rs1796948871"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547310,"source":"dbSNP","strand":1,"feature_type":"variation","end":140547310,"alleles":["A","G"],"seq_region_name":"7","id":"rs1796948971","clinical_significance":[]},{"clinical_significance":[],"id":"rs2130531169","seq_region_name":"7","source":"dbSNP","start":140547311,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140547311,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs537615669","source":"dbSNP","start":140547312,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C","G"],"end":140547312,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130531189","alleles":["G","A"],"end":140547313,"feature_type":"variation","strand":1,"source":"dbSNP","start":140547313,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140547315,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140547315,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1796949232","seq_region_name":"7"},{"start":140547317,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TTT","TTTT"],"end":140547319,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs34719029","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs866859778","source":"dbSNP","start":140547319,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140547319,"alleles":["T","C"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547324,"source":"dbSNP","strand":1,"feature_type":"variation","end":140547324,"alleles":["C","G"],"seq_region_name":"7","id":"rs1796949518","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547335,"feature_type":"variation","strand":1,"end":140547335,"alleles":["G","C"],"clinical_significance":[],"id":"rs1796949626","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1363733316","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547338,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140547338},{"id":"rs934612434","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140547344,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547344,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140547346,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547346,"source":"dbSNP","id":"rs1563131329","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796950064","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547356,"source":"dbSNP","strand":1,"feature_type":"variation","end":140547356,"alleles":["T","C"]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140547361,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547361,"clinical_significance":[],"seq_region_name":"7","id":"rs1796950193"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547363,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140547363,"seq_region_name":"7","id":"rs1796950286","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796950394","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547373,"source":"dbSNP","strand":1,"feature_type":"variation","end":140547410,"alleles":["ATGAAAATGTCATGGGAGGGGATAGCCATCATGAAAAT","ATGAAAAT"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547378,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140547378,"clinical_significance":[],"seq_region_name":"7","id":"rs1796950478"},{"id":"rs1796950584","seq_region_name":"7","clinical_significance":[],"start":140547379,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140547379,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs937898225","clinical_significance":[],"start":140547380,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140547380,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585599363","alleles":["A","G"],"end":140547384,"feature_type":"variation","strand":1,"source":"dbSNP","start":140547384,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1796950910","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140547386,"strand":1,"feature_type":"variation","start":140547386,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796951010","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547388,"feature_type":"variation","strand":1,"end":140547388,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1055019460","clinical_significance":[],"alleles":["G","C"],"end":140547390,"strand":1,"feature_type":"variation","start":140547390,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1399232488","clinical_significance":[],"strand":1,"feature_type":"variation","end":140547393,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547393,"source":"dbSNP"},{"alleles":["T","C"],"end":140547395,"feature_type":"variation","strand":1,"source":"dbSNP","start":140547395,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1376287610","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1796951443","clinical_significance":[],"strand":1,"feature_type":"variation","end":140547401,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547401,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs894496738","source":"dbSNP","start":140547403,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G","T"],"end":140547403,"feature_type":"variation","strand":1},{"end":140547404,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140547404,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1432922949"},{"end":140547408,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140547408,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs931264345"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547415,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140547415,"seq_region_name":"7","id":"rs1313914838","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140547423,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547423,"source":"dbSNP","seq_region_name":"7","id":"rs747420920","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547425,"source":"dbSNP","strand":1,"feature_type":"variation","end":140547425,"alleles":["C","T"],"seq_region_name":"7","id":"rs1430819662","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140547426,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547426,"source":"dbSNP","seq_region_name":"7","id":"rs1796952221","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547427,"feature_type":"variation","strand":1,"end":140547427,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs781337414"},{"start":140547428,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140547428,"alleles":["T","C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1215503726","clinical_significance":[]},{"id":"rs553574314","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140547431,"strand":1,"feature_type":"variation","start":140547431,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1306231083","seq_region_name":"7","source":"dbSNP","start":140547432,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140547432,"feature_type":"variation","strand":1},{"start":140547433,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140547433,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796952820","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796952938","source":"dbSNP","start":140547436,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140547436,"alleles":["C","G"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547437,"feature_type":"variation","strand":1,"end":140547437,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs748249494"},{"alleles":["C","T"],"end":140547438,"feature_type":"variation","strand":1,"source":"dbSNP","start":140547438,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1481965661"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140547443,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547443,"source":"dbSNP","seq_region_name":"7","id":"rs1004830317","clinical_significance":[]},{"seq_region_name":"7","id":"rs1019764290","clinical_significance":[],"start":140547445,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140547445,"alleles":["C","A","G","T"],"strand":1,"feature_type":"variation"},{"end":140547447,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140547447,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs901463846","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547448,"feature_type":"variation","strand":1,"end":140547448,"alleles":["G","A"],"clinical_significance":[],"id":"rs997069707","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796953729","feature_type":"variation","strand":1,"end":140547458,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547458},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547461,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140547461,"clinical_significance":[],"seq_region_name":"7","id":"rs1028491713"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130531535","feature_type":"variation","strand":1,"end":140547461,"alleles":["T","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547461},{"start":140547468,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140547468,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs957707305","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140547472,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547472,"source":"dbSNP","id":"rs1355908666","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1295302245","alleles":["G","A"],"end":140547473,"feature_type":"variation","strand":1,"source":"dbSNP","start":140547473,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140547475,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547475,"clinical_significance":[],"seq_region_name":"7","id":"rs1394544614"},{"source":"dbSNP","start":140547482,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140547482,"alleles":["C","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796954270"},{"alleles":["G","A","T"],"end":140547485,"strand":1,"feature_type":"variation","start":140547485,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796954360","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1462714539","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140547486,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547486},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547488,"source":"dbSNP","strand":1,"feature_type":"variation","end":140547488,"alleles":["T","C"],"seq_region_name":"7","id":"rs1796954591","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547490,"source":"dbSNP","strand":1,"feature_type":"variation","end":140547490,"alleles":["G","-"],"seq_region_name":"7","id":"rs1796954718","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796954823","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547497,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140547497},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796954943","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140547499,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547499},{"clinical_significance":[],"seq_region_name":"7","id":"rs1010562153","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140547500,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547500},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547501,"feature_type":"variation","strand":1,"end":140547501,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1796955159"},{"alleles":["G","C","T"],"end":140547502,"feature_type":"variation","strand":1,"source":"dbSNP","start":140547502,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs962490028","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1298803766","seq_region_name":"7","alleles":["G","T"],"end":140547504,"feature_type":"variation","strand":1,"source":"dbSNP","start":140547504,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["A","G"],"end":140547505,"feature_type":"variation","strand":1,"source":"dbSNP","start":140547505,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1047933206"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547507,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140547507,"clinical_significance":[],"seq_region_name":"7","id":"rs1796955596"},{"feature_type":"variation","strand":1,"end":140547510,"alleles":["ATTA","ATTATTA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547507,"clinical_significance":[],"seq_region_name":"7","id":"rs1796955695"},{"seq_region_name":"7","id":"rs1796955868","clinical_significance":[],"start":140547508,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140547509,"alleles":["TT","T"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547520,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140547520,"id":"rs2130531711","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","T"],"end":140547527,"strand":1,"feature_type":"variation","start":140547527,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796956049","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547530,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140547530,"clinical_significance":[],"seq_region_name":"7","id":"rs1796956210"},{"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140547545,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547545,"clinical_significance":[],"seq_region_name":"7","id":"rs1796956380"},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140547546,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547546,"source":"dbSNP","seq_region_name":"7","id":"rs1021160796","clinical_significance":[]},{"seq_region_name":"7","id":"rs1563131433","clinical_significance":[],"start":140547553,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140547553,"alleles":["T","G"],"strand":1,"feature_type":"variation"},{"start":140547554,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C","G","T"],"end":140547554,"strand":1,"feature_type":"variation","id":"rs75350819","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796957194","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547557,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140547557},{"start":140547558,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140547558,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs966468562","clinical_significance":[]},{"clinical_significance":[],"id":"rs886777667","seq_region_name":"7","source":"dbSNP","start":140547561,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140547561,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["AA","A"],"end":140547564,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547563,"clinical_significance":[],"seq_region_name":"7","id":"rs1796957654"},{"id":"rs1585599738","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547566,"source":"dbSNP","strand":1,"feature_type":"variation","end":140547566,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs74898279","alleles":["T","C"],"end":140547570,"feature_type":"variation","strand":1,"source":"dbSNP","start":140547570,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140547571,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140547571,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1796958174","seq_region_name":"7","clinical_significance":[]},{"end":140547578,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140547578,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs61427927","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796958596","end":140547580,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140547580,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","G"],"end":140547581,"strand":1,"feature_type":"variation","start":140547581,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1177271468","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585599784","alleles":["A","G"],"end":140547582,"feature_type":"variation","strand":1,"source":"dbSNP","start":140547582,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["G","A","T"],"end":140547586,"feature_type":"variation","strand":1,"source":"dbSNP","start":140547586,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1481351745"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547587,"feature_type":"variation","strand":1,"end":140547587,"alleles":["G","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs959168780"},{"feature_type":"variation","strand":1,"end":140547593,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547593,"clinical_significance":[],"id":"rs1796959173","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1796959277","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547594,"source":"dbSNP","strand":1,"feature_type":"variation","end":140547594,"alleles":["A","G"]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140547595,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547595,"clinical_significance":[],"seq_region_name":"7","id":"rs990739280"},{"end":140547596,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140547596,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1464980973"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796959609","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140547600,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547600},{"seq_region_name":"7","id":"rs1242410373","clinical_significance":[],"start":140547602,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140547602,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796959816","end":140547604,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140547604,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140547606,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140547606,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs920477488"},{"clinical_significance":[],"seq_region_name":"7","id":"rs931340455","end":140547611,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140547611,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs968659366","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140547614,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547614},{"seq_region_name":"7","id":"rs1393188664","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547618,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140547618},{"clinical_significance":[],"seq_region_name":"7","id":"rs1374794172","feature_type":"variation","strand":1,"end":140547620,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547620},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130531956","feature_type":"variation","strand":1,"alleles":["G","-"],"end":140547622,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547622},{"id":"rs745764724","seq_region_name":"7","clinical_significance":[],"end":140547623,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140547623,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796960538","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547627,"feature_type":"variation","strand":1,"end":140547627,"alleles":["C","G"]},{"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140547629,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547629,"clinical_significance":[],"seq_region_name":"7","id":"rs1331216020"},{"start":140547632,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140547632,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796960760","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1462428955","feature_type":"variation","strand":1,"end":140547639,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547639},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547640,"source":"dbSNP","strand":1,"feature_type":"variation","end":140547640,"alleles":["C","G"],"seq_region_name":"7","id":"rs1449823974","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547646,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140547646,"clinical_significance":[],"seq_region_name":"7","id":"rs1796961104"},{"clinical_significance":[],"seq_region_name":"7","id":"rs978681358","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547649,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140547649},{"seq_region_name":"7","id":"rs1796961324","clinical_significance":[],"alleles":["T","C","G"],"end":140547650,"strand":1,"feature_type":"variation","start":140547650,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1332989087","clinical_significance":[],"start":140547657,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","-"],"end":140547657,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1326625646","source":"dbSNP","start":140547659,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140547659,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547660,"feature_type":"variation","strand":1,"end":140547660,"alleles":["T","C"],"clinical_significance":[],"id":"rs1457779091","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547662,"feature_type":"variation","strand":1,"end":140547662,"alleles":["T","C"],"clinical_significance":[],"id":"rs1367499752","seq_region_name":"7"},{"start":140547667,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140547667,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1159446956","clinical_significance":[]},{"end":140547668,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140547668,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1420306477","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547669,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140547669,"clinical_significance":[],"seq_region_name":"7","id":"rs1235866279"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547676,"feature_type":"variation","strand":1,"end":140547676,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs75172007"},{"alleles":["C","A"],"end":140547682,"strand":1,"feature_type":"variation","start":140547682,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1796962632","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","G"],"end":140547683,"feature_type":"variation","strand":1,"source":"dbSNP","start":140547683,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1468872759","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140547684,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547684,"source":"dbSNP","id":"rs1796962871","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1254883820","feature_type":"variation","strand":1,"end":140547686,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547686},{"seq_region_name":"7","id":"rs908646020","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547687,"source":"dbSNP","strand":1,"feature_type":"variation","end":140547687,"alleles":["T","C"]},{"id":"rs373341700","seq_region_name":"7","clinical_significance":[],"end":140547694,"alleles":["TGTCTGT","TGT"],"strand":1,"feature_type":"variation","start":140547688,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["T","C"],"end":140547692,"strand":1,"feature_type":"variation","start":140547692,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796963183","clinical_significance":[]},{"end":140547693,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140547693,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1360331140","clinical_significance":[]},{"clinical_significance":[],"id":"rs73487670","seq_region_name":"7","feature_type":"variation","strand":1,"end":140547697,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547697},{"clinical_significance":[],"id":"rs375983567","seq_region_name":"7","source":"dbSNP","start":140547698,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140547698,"alleles":["G","A","C"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547702,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140547702,"seq_region_name":"7","id":"rs1796963567","clinical_significance":[]},{"id":"rs1351514635","seq_region_name":"7","clinical_significance":[],"end":140547705,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140547705,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1326341733","clinical_significance":[],"end":140547706,"alleles":["TT","T"],"strand":1,"feature_type":"variation","start":140547705,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs901370466","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547713,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140547713},{"start":140547714,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140547714,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs996935014","clinical_significance":[]},{"id":"rs917349096","seq_region_name":"7","clinical_significance":[],"start":140547719,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140547719,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547720,"source":"dbSNP","strand":1,"feature_type":"variation","end":140547720,"alleles":["A","G"],"seq_region_name":"7","id":"rs1049999395","clinical_significance":[]},{"alleles":["C","T"],"end":140547721,"strand":1,"feature_type":"variation","start":140547721,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796964263","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140547729,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547729,"source":"dbSNP","id":"rs1796964388","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547736,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140547736,"id":"rs1796964523","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547737,"feature_type":"variation","strand":1,"end":140547737,"alleles":["A","G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1278043753"},{"id":"rs180799384","seq_region_name":"7","clinical_significance":[],"end":140547738,"alleles":["T","C","G"],"strand":1,"feature_type":"variation","start":140547738,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796964948","source":"dbSNP","start":140547739,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140547739,"feature_type":"variation","strand":1},{"end":140547743,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140547743,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs780551454","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140547747,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547747,"clinical_significance":[],"seq_region_name":"7","id":"rs1011009967"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796965254","alleles":["C","-"],"end":140547748,"feature_type":"variation","strand":1,"source":"dbSNP","start":140547748,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["T","A"],"end":140547749,"strand":1,"feature_type":"variation","start":140547749,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs561663075","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1386166578","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140547750,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547750,"source":"dbSNP"},{"id":"rs1195613392","seq_region_name":"7","clinical_significance":[],"end":140547758,"alleles":["GTG","G"],"strand":1,"feature_type":"variation","start":140547756,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140547758,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140547758,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1044997515","clinical_significance":[]},{"id":"rs1240073302","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547761,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140547761},{"clinical_significance":[],"seq_region_name":"7","id":"rs920771868","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547765,"feature_type":"variation","strand":1,"end":140547765,"alleles":["A","C"]},{"seq_region_name":"7","id":"rs1020605267","clinical_significance":[],"start":140547773,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140547773,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs529226314","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547779,"feature_type":"variation","strand":1,"end":140547779,"alleles":["C","A","T"]},{"seq_region_name":"7","id":"rs1196689864","clinical_significance":[],"alleles":["A","T"],"end":140547781,"strand":1,"feature_type":"variation","start":140547781,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1796966415","clinical_significance":[],"start":140547784,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140547784,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs2130532404","clinical_significance":[],"end":140547785,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140547785,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1199949169","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547787,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140547787},{"seq_region_name":"7","id":"rs571482846","clinical_significance":[],"alleles":["G","A","C"],"end":140547788,"strand":1,"feature_type":"variation","start":140547788,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1207058593","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547790,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140547790},{"clinical_significance":[],"seq_region_name":"7","id":"rs144335173","alleles":["A","G"],"end":140547791,"feature_type":"variation","strand":1,"source":"dbSNP","start":140547791,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1796967239","clinical_significance":[],"end":140547793,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140547793,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1796967406","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547796,"source":"dbSNP","strand":1,"feature_type":"variation","end":140547796,"alleles":["A","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1285665056","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547807,"feature_type":"variation","strand":1,"alleles":["AAA","AAAAA"],"end":140547809},{"start":140547809,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140547809,"alleles":["A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796967741","clinical_significance":[]},{"seq_region_name":"7","id":"rs1171444720","clinical_significance":[],"start":140547813,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140547813,"strand":1,"feature_type":"variation"},{"start":140547815,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140547815,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs1796968068","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796968224","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547819,"feature_type":"variation","strand":1,"end":140547819,"alleles":["C","T"]},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140547820,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547820,"source":"dbSNP","seq_region_name":"7","id":"rs1737170413","clinical_significance":[]},{"start":140547823,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140547823,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585600353","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1385082575","source":"dbSNP","start":140547829,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140547829,"alleles":["C","G"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547833,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140547833,"clinical_significance":[],"seq_region_name":"7","id":"rs1350208099"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796968656","source":"dbSNP","start":140547834,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140547834,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1796968741","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140547836,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547836,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140547840,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547840,"source":"dbSNP","id":"rs959201709","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140547842,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547842,"clinical_significance":[],"seq_region_name":"7","id":"rs1233203429"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796969092","feature_type":"variation","strand":1,"end":140547843,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547843},{"start":140547843,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["GAAAACATTATGCTAAATG","-"],"end":140547861,"strand":1,"feature_type":"variation","id":"rs1402027633","seq_region_name":"7","clinical_significance":[]},{"start":140547852,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140547852,"alleles":["A","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796969310","clinical_significance":[]},{"seq_region_name":"7","id":"rs990645789","clinical_significance":[],"end":140547853,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","start":140547853,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140547853,"alleles":["T","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547853,"clinical_significance":[],"id":"rs1796969555","seq_region_name":"7"},{"id":"rs920549632","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547861,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140547861},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140547865,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547865,"source":"dbSNP","seq_region_name":"7","id":"rs1796969761","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547867,"source":"dbSNP","strand":1,"feature_type":"variation","end":140547867,"alleles":["A","G"],"seq_region_name":"7","id":"rs1796969866","clinical_significance":[]},{"id":"rs1320711845","seq_region_name":"7","clinical_significance":[],"end":140547869,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140547869,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1315793281","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547870,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140547870},{"start":140547873,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140547873,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs538900167","clinical_significance":[]},{"seq_region_name":"7","id":"rs1297248366","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547881,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140547881},{"end":140547883,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140547883,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1434741849","clinical_significance":[]},{"seq_region_name":"7","id":"rs1403754639","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140547884,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547884,"source":"dbSNP"},{"start":140547886,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TCT","T"],"end":140547888,"strand":1,"feature_type":"variation","id":"rs1399769298","seq_region_name":"7","clinical_significance":[]},{"start":140547887,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["CTAA","-"],"end":140547890,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1170673883","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547890,"source":"dbSNP","strand":1,"feature_type":"variation","end":140547891,"alleles":["AT","-"],"id":"rs1284372014","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1477664773","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547891,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140547891},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547892,"feature_type":"variation","strand":1,"end":140547892,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs559526625"},{"id":"rs1195568313","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140547895,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547895,"source":"dbSNP"},{"seq_region_name":"7","id":"rs968540324","clinical_significance":[],"end":140547897,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140547897,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1262719059","clinical_significance":[],"start":140547899,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140547899,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs7782049","end":140547900,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140547900,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1274269643","seq_region_name":"7","clinical_significance":[],"start":140547901,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140547901,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs2130532762","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547903,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140547903},{"source":"dbSNP","start":140547907,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140547907,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796971678"},{"source":"dbSNP","start":140547909,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C","G"],"end":140547909,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs939993816","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796971921","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547912,"feature_type":"variation","strand":1,"end":140547912,"alleles":["A","T"]},{"alleles":["T","C"],"end":140547914,"feature_type":"variation","strand":1,"source":"dbSNP","start":140547914,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1340665476"},{"seq_region_name":"7","id":"rs955926090","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547918,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140547918},{"seq_region_name":"7","id":"rs1796972247","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547922,"source":"dbSNP","strand":1,"feature_type":"variation","end":140547922,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs1217157288","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547923,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140547923},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547930,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140547930,"clinical_significance":[],"seq_region_name":"7","id":"rs1041116932"},{"id":"rs922678852","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140547933,"strand":1,"feature_type":"variation","start":140547933,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs368331466","clinical_significance":[],"start":140547934,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140547934,"strand":1,"feature_type":"variation"},{"end":140547937,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140547937,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1415022135"},{"seq_region_name":"7","id":"rs1341678325","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547938,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140547938},{"alleles":["C","A"],"end":140547941,"strand":1,"feature_type":"variation","start":140547941,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1331605095","clinical_significance":[]},{"start":140547943,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140547943,"alleles":["G","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796973119","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs932858311","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140547944,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547944},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140547952,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547952,"source":"dbSNP","seq_region_name":"7","id":"rs970581283","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547955,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140547955,"seq_region_name":"7","id":"rs1397087999","clinical_significance":[]},{"seq_region_name":"7","id":"rs1172796604","clinical_significance":[],"alleles":["G","T"],"end":140547958,"strand":1,"feature_type":"variation","start":140547958,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1796973676","clinical_significance":[],"start":140547967,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140547967,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1463823224","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547970,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140547970},{"seq_region_name":"7","id":"rs980213489","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547971,"source":"dbSNP","strand":1,"feature_type":"variation","end":140547971,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs57960333","alleles":["G","A"],"end":140547973,"feature_type":"variation","strand":1,"source":"dbSNP","start":140547973,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140547977,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547977,"clinical_significance":[],"seq_region_name":"7","id":"rs1796974110"},{"end":140547979,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140547979,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796974207"},{"clinical_significance":[],"seq_region_name":"7","id":"rs185431246","alleles":["C","A","T"],"end":140547980,"feature_type":"variation","strand":1,"source":"dbSNP","start":140547980,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547981,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140547981,"clinical_significance":[],"seq_region_name":"7","id":"rs908156657"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796974521","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140547982,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140547982},{"seq_region_name":"7","id":"rs1479389121","clinical_significance":[],"start":140547991,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140547991,"alleles":["T","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs74723088","clinical_significance":[],"end":140547993,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140547993,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1275659532","end":140547997,"alleles":["GGG","GG"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140547995,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1363804004","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547998,"source":"dbSNP","strand":1,"feature_type":"variation","end":140547998,"alleles":["T","G"]},{"seq_region_name":"7","id":"rs1197332195","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140547999,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140547999,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140548005,"alleles":["T","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548005,"clinical_significance":[],"seq_region_name":"7","id":"rs1796975150"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548007,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140548007,"clinical_significance":[],"seq_region_name":"7","id":"rs1317600058"},{"seq_region_name":"7","id":"rs1470877318","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548011,"source":"dbSNP","strand":1,"feature_type":"variation","end":140548011,"alleles":["T","G"]},{"seq_region_name":"7","id":"rs1274211356","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140548014,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548014,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1235592852","alleles":["G","A"],"end":140548015,"feature_type":"variation","strand":1,"source":"dbSNP","start":140548015,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140548022,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548022,"source":"dbSNP","seq_region_name":"7","id":"rs1358019042","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796975778","clinical_significance":[],"start":140548035,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140548035,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"alleles":["G","A","C"],"end":140548044,"feature_type":"variation","strand":1,"source":"dbSNP","start":140548044,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs776202907"},{"seq_region_name":"7","id":"rs1041141050","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548046,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140548046},{"seq_region_name":"7","id":"rs1796976155","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548052,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140548052},{"start":140548058,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140548058,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1333242887","clinical_significance":[]},{"seq_region_name":"7","id":"rs900841805","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140548061,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548061,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140548063,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548063,"clinical_significance":[],"seq_region_name":"7","id":"rs762758494"},{"seq_region_name":"7","id":"rs2130533133","clinical_significance":[],"strand":1,"feature_type":"variation","end":140548065,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548065,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140548067,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548067,"source":"dbSNP","id":"rs1049514169","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548070,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140548070,"id":"rs1406946380","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs904245929","clinical_significance":[],"alleles":["A","T"],"end":140548072,"strand":1,"feature_type":"variation","start":140548072,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1796976925","clinical_significance":[],"start":140548073,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140548073,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548074,"source":"dbSNP","strand":1,"feature_type":"variation","end":140548074,"alleles":["T","G"],"seq_region_name":"7","id":"rs1304078171","clinical_significance":[]},{"source":"dbSNP","start":140548078,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140548078,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1043008753"},{"id":"rs1796977225","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140548079,"strand":1,"feature_type":"variation","start":140548079,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1796977345","clinical_significance":[],"start":140548081,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140548081,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796977472","source":"dbSNP","start":140548082,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140548082,"alleles":["A","C"],"feature_type":"variation","strand":1},{"start":140548084,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140548084,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796977639","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1367861377","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548085,"feature_type":"variation","strand":1,"end":140548085,"alleles":["T","C"]},{"clinical_significance":[],"id":"rs796415513","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548085,"feature_type":"variation","strand":1,"alleles":["TATTTTTTATTTTTTATT","TATTTTTTATT","TATTTTTTATTTTTTATTTTTTATT"],"end":140548102},{"id":"rs1177250736","seq_region_name":"7","clinical_significance":[],"start":140548086,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140548086,"alleles":["A","AA"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1385526245","source":"dbSNP","start":140548091,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140548091,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140548092,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548092,"source":"dbSNP","seq_region_name":"7","id":"rs2130533276","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1457699096","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140548093,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548093},{"seq_region_name":"7","id":"rs1796978677","clinical_significance":[],"start":140548096,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140548096,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796978856","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548101,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140548101},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548107,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140548107,"clinical_significance":[],"id":"rs1796979010","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796979147","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140548123,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548123},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548124,"feature_type":"variation","strand":1,"end":140548124,"alleles":["C","A","G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs35196803"},{"start":140548127,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140548127,"alleles":["G","T"],"strand":1,"feature_type":"variation","id":"rs549015553","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs902178105","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548129,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140548129},{"start":140548130,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140548130,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs567545995","clinical_significance":[]},{"seq_region_name":"7","id":"rs553798479","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140548131,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548131,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140548133,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548133,"source":"dbSNP","id":"rs535365034","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140548134,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548134,"clinical_significance":[],"seq_region_name":"7","id":"rs1796980026"},{"end":140548135,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140548135,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796980140","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs80338199","end":140548137,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140548137,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140548138,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140548138,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1350685097"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1012110962","feature_type":"variation","strand":1,"end":140548148,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548148},{"seq_region_name":"7","id":"rs578133482","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548151,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140548151},{"start":140548152,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140548152,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1796980715","clinical_significance":[]},{"end":140548156,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140548156,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs539192775","clinical_significance":[]},{"start":140548159,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140548159,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs951944846","clinical_significance":[]},{"end":140548162,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140548162,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1796981014","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1326547201","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548163,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140548163},{"clinical_significance":[],"id":"rs1438283009","seq_region_name":"7","alleles":["C","T"],"end":140548166,"feature_type":"variation","strand":1,"source":"dbSNP","start":140548166,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140548169,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140548169,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs980481274","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","T"],"end":140548170,"feature_type":"variation","strand":1,"source":"dbSNP","start":140548170,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1323062264"},{"source":"dbSNP","start":140548172,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140548172,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs2130533502","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1027722988","clinical_significance":[],"alleles":["T","A","C"],"end":140548173,"strand":1,"feature_type":"variation","start":140548173,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548175,"feature_type":"variation","strand":1,"end":140548175,"alleles":["T","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1796981609"},{"seq_region_name":"7","id":"rs1796981700","clinical_significance":[],"strand":1,"feature_type":"variation","end":140548177,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548177,"source":"dbSNP"},{"start":140548179,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140548179,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs983407574","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548190,"feature_type":"variation","strand":1,"end":140548190,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1796981910"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548191,"source":"dbSNP","strand":1,"feature_type":"variation","end":140548191,"alleles":["C","T"],"seq_region_name":"7","id":"rs1209091588","clinical_significance":[]},{"seq_region_name":"7","id":"rs1015217784","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548193,"source":"dbSNP","strand":1,"feature_type":"variation","end":140548193,"alleles":["G","A"]},{"strand":1,"feature_type":"variation","end":140548194,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548194,"source":"dbSNP","seq_region_name":"7","id":"rs1585601253","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140548198,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548198,"clinical_significance":[],"seq_region_name":"7","id":"rs1796982384"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548200,"source":"dbSNP","strand":1,"feature_type":"variation","end":140548200,"alleles":["C","A"],"seq_region_name":"7","id":"rs1796982480","clinical_significance":[]},{"seq_region_name":"7","id":"rs961433171","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548205,"source":"dbSNP","strand":1,"feature_type":"variation","end":140548205,"alleles":["G","A"]},{"id":"rs1796982699","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140548207,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548207,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130533601","end":140548210,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140548210,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140548212,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548212,"source":"dbSNP","seq_region_name":"7","id":"rs1796982796","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796982902","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548221,"feature_type":"variation","strand":1,"end":140548221,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs908040641","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548227,"feature_type":"variation","strand":1,"end":140548227,"alleles":["T","C"]},{"end":140548229,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140548229,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1796983124","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs944834865","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140548233,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548233},{"feature_type":"variation","strand":1,"end":140548234,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548234,"clinical_significance":[],"id":"rs1796983356","seq_region_name":"7"},{"end":140548241,"alleles":["TAAAT","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140548237,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1487687169","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1796983465","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548238,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140548238},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140548241,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548241,"clinical_significance":[],"seq_region_name":"7","id":"rs1246495312"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796983701","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548245,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140548245},{"seq_region_name":"7","id":"rs1796983816","clinical_significance":[],"strand":1,"feature_type":"variation","end":140548246,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548246,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1796983931","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548247,"source":"dbSNP","strand":1,"feature_type":"variation","end":140548247,"alleles":["A","C","G"]},{"seq_region_name":"7","id":"rs976716331","clinical_significance":[],"alleles":["T","A","C"],"end":140548249,"strand":1,"feature_type":"variation","start":140548249,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1488407395","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548251,"source":"dbSNP","strand":1,"feature_type":"variation","end":140548251,"alleles":["G","A"]},{"source":"dbSNP","start":140548254,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140548254,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs922711281","seq_region_name":"7"},{"start":140548259,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140548259,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs557887775","clinical_significance":[]},{"seq_region_name":"7","id":"rs932722694","clinical_significance":[],"start":140548260,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140548260,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140548262,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548262,"source":"dbSNP","id":"rs1213792713","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs576249659","clinical_significance":[],"alleles":["A","T"],"end":140548267,"strand":1,"feature_type":"variation","start":140548267,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548273,"feature_type":"variation","strand":1,"end":140548278,"alleles":["TAATAA","TAA"],"clinical_significance":[],"seq_region_name":"7","id":"rs1796984795"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548274,"feature_type":"variation","strand":1,"end":140548275,"alleles":["AA","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs749006718"},{"alleles":["T","A"],"end":140548276,"strand":1,"feature_type":"variation","start":140548276,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1030566557","clinical_significance":[]},{"source":"dbSNP","start":140548278,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140548278,"alleles":["A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs985481354"},{"start":140548280,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140548280,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs915430394","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140548281,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548281,"clinical_significance":[],"seq_region_name":"7","id":"rs189945049"},{"strand":1,"feature_type":"variation","end":140548287,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548287,"source":"dbSNP","seq_region_name":"7","id":"rs1042650839","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548289,"feature_type":"variation","strand":1,"alleles":["AAAAAA","AAAAA","AAAAAAA"],"end":140548294,"clinical_significance":[],"seq_region_name":"7","id":"rs1796985516"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1274013494","end":140548290,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140548290,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1796985749","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548291,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140548291},{"start":140548294,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C","G"],"end":140548294,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1431288718","clinical_significance":[]},{"alleles":["C","A"],"end":140548295,"feature_type":"variation","strand":1,"source":"dbSNP","start":140548295,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1383068380"},{"seq_region_name":"7","id":"rs1165089813","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548295,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CT","-"],"end":140548296},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796986214","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548296,"feature_type":"variation","strand":1,"alleles":["-","A"],"end":140548295},{"clinical_significance":[],"seq_region_name":"7","id":"rs954706424","feature_type":"variation","strand":1,"end":140548296,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548296},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796986408","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548296,"feature_type":"variation","strand":1,"alleles":["T","-"],"end":140548296},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796986524","alleles":["TA","-"],"end":140548297,"feature_type":"variation","strand":1,"source":"dbSNP","start":140548296,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1796986637","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548297,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140548297},{"id":"rs34963245","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140548313,"alleles":["AAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAA","AAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548297,"source":"dbSNP"},{"source":"dbSNP","start":140548299,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140548299,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs9768386"},{"seq_region_name":"7","id":"rs1187470135","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548305,"source":"dbSNP","strand":1,"feature_type":"variation","end":140548304,"alleles":["-","C"]},{"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140548308,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548308,"source":"dbSNP","seq_region_name":"7","id":"rs1796987427","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796987581","feature_type":"variation","strand":1,"alleles":["-","G"],"end":140548313,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548314},{"clinical_significance":[],"seq_region_name":"7","id":"rs1263538824","end":140548314,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140548314,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140548319,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140548319,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796987907"},{"seq_region_name":"7","id":"rs1796988051","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548332,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140548332},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548333,"source":"dbSNP","strand":1,"feature_type":"variation","end":140548333,"alleles":["T","A"],"seq_region_name":"7","id":"rs2130533998","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796988210","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140548336,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548336},{"alleles":["AGAG","AG"],"end":140548350,"feature_type":"variation","strand":1,"source":"dbSNP","start":140548347,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs932349984","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1796988526","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140548348,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548348,"source":"dbSNP"},{"seq_region_name":"7","id":"rs902757253","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548349,"source":"dbSNP","strand":1,"feature_type":"variation","end":140548349,"alleles":["A","C","G"]},{"clinical_significance":[],"id":"rs1585601580","seq_region_name":"7","source":"dbSNP","start":140548351,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140548351,"alleles":["T","G"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548355,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140548355,"id":"rs1796989058","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548361,"source":"dbSNP","strand":1,"feature_type":"variation","end":140548361,"alleles":["A","C"],"seq_region_name":"7","id":"rs1796989227","clinical_significance":[]},{"id":"rs1397802152","seq_region_name":"7","clinical_significance":[],"end":140548366,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140548366,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548367,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140548367,"clinical_significance":[],"seq_region_name":"7","id":"rs1408759904"},{"start":140548368,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140548368,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs939038884","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140548377,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548377,"clinical_significance":[],"id":"rs1056125376","seq_region_name":"7"},{"seq_region_name":"7","id":"rs894928066","clinical_significance":[],"strand":1,"feature_type":"variation","end":140548382,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548382,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1393680497","feature_type":"variation","strand":1,"end":140548388,"alleles":["G","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548388},{"strand":1,"feature_type":"variation","end":140548389,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548389,"source":"dbSNP","seq_region_name":"7","id":"rs1012018152","clinical_significance":[]},{"clinical_significance":[],"id":"rs1796990227","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548391,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140548391},{"seq_region_name":"7","id":"rs1329343688","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548394,"source":"dbSNP","strand":1,"feature_type":"variation","end":140548394,"alleles":["C","T"]},{"source":"dbSNP","start":140548395,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140548395,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1027795141"},{"clinical_significance":[],"seq_region_name":"7","id":"rs113342782","source":"dbSNP","start":140548400,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140548400,"alleles":["T","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1585601680","clinical_significance":[],"start":140548401,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140548401,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1342167953","clinical_significance":[],"alleles":["C","A"],"end":140548406,"strand":1,"feature_type":"variation","start":140548406,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1276496697","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548407,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140548407},{"start":140548408,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C"],"end":140548408,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1399634752","clinical_significance":[]},{"id":"rs2130534167","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140548416,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548416,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548417,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140548417,"seq_region_name":"7","id":"rs1005114254","clinical_significance":[]},{"source":"dbSNP","start":140548420,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140548420,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1796991133"},{"alleles":["C","G"],"end":140548421,"feature_type":"variation","strand":1,"source":"dbSNP","start":140548421,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1796991252","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548424,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140548424,"clinical_significance":[],"seq_region_name":"7","id":"rs1796991352"},{"seq_region_name":"7","id":"rs1356108871","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548428,"source":"dbSNP","strand":1,"feature_type":"variation","end":140548428,"alleles":["A","C","G"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548429,"source":"dbSNP","strand":1,"feature_type":"variation","end":140548429,"alleles":["G","C"],"seq_region_name":"7","id":"rs557207714","clinical_significance":[]},{"source":"dbSNP","start":140548429,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["GG","GGG"],"end":140548430,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585601747"},{"seq_region_name":"7","id":"rs1585601758","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548431,"source":"dbSNP","strand":1,"feature_type":"variation","end":140548431,"alleles":["A","G"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548432,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140548432,"id":"rs2130534237","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140548436,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140548436,"alleles":["T","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1585601774","seq_region_name":"7"},{"id":"rs935735127","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548438,"source":"dbSNP","strand":1,"feature_type":"variation","end":140548438,"alleles":["C","A"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548442,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140548442,"clinical_significance":[],"id":"rs1563132162","seq_region_name":"7"},{"end":140548444,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140548444,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1464669477"},{"end":140548446,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140548446,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1359067984"},{"seq_region_name":"7","id":"rs1171794901","clinical_significance":[],"end":140548452,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140548452,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140548462,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140548462,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1467471140","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140548463,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548463,"source":"dbSNP","id":"rs1796992532","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796992616","clinical_significance":[],"start":140548468,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140548468,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"alleles":["C","T"],"end":140548469,"strand":1,"feature_type":"variation","start":140548469,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1421936187","clinical_significance":[]},{"source":"dbSNP","start":140548478,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A","C"],"end":140548478,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs966334589","seq_region_name":"7"},{"start":140548480,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G","T"],"end":140548480,"strand":1,"feature_type":"variation","id":"rs114332362","seq_region_name":"7","clinical_significance":[]},{"start":140548480,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140548486,"alleles":["CCACCAC","CCACCACCAC"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1317423498","clinical_significance":[]},{"id":"rs1796993231","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140548482,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548482,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140548483,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548483,"clinical_significance":[],"id":"rs1243769170","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140548488,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548488,"source":"dbSNP","id":"rs905761011","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs559351252","end":140548490,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140548490,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs763393684","clinical_significance":[],"end":140548495,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140548495,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1319652710","seq_region_name":"7","end":140548501,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140548501,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548504,"feature_type":"variation","strand":1,"end":140548504,"alleles":["A","G"],"clinical_significance":[],"id":"rs1796993757","seq_region_name":"7"},{"seq_region_name":"7","id":"rs182840493","clinical_significance":[],"start":140548505,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140548505,"alleles":["T","C","G"],"strand":1,"feature_type":"variation"},{"id":"rs1796993999","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548505,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","-"],"end":140548505},{"clinical_significance":[],"id":"rs1027608688","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140548506,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548506},{"clinical_significance":[],"seq_region_name":"7","id":"rs954023495","feature_type":"variation","strand":1,"end":140548511,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548511},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548523,"source":"dbSNP","strand":1,"feature_type":"variation","end":140548523,"alleles":["A","G"],"id":"rs1796994316","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1796994396","seq_region_name":"7","source":"dbSNP","start":140548528,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140548528,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140548530,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548530,"clinical_significance":[],"id":"rs1796994501","seq_region_name":"7"},{"start":140548534,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140548534,"alleles":["C","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs370023691","clinical_significance":[]},{"alleles":["T","C"],"end":140548540,"feature_type":"variation","strand":1,"source":"dbSNP","start":140548540,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796994715"},{"end":140548541,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140548541,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796994807","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140548543,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548543,"source":"dbSNP","seq_region_name":"7","id":"rs1585602025","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130534490","clinical_significance":[],"alleles":["T","C"],"end":140548544,"strand":1,"feature_type":"variation","start":140548544,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140548545,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140548545,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585602042","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585602060","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140548547,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548547,"source":"dbSNP"},{"seq_region_name":"7","id":"rs952162817","clinical_significance":[],"start":140548548,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140548548,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140548549,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548549,"source":"dbSNP","seq_region_name":"7","id":"rs1585602086","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140548550,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548550,"clinical_significance":[],"seq_region_name":"7","id":"rs1341325326"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548551,"source":"dbSNP","strand":1,"feature_type":"variation","end":140548550,"alleles":["-","TCA"],"seq_region_name":"7","id":"rs1585602110","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548556,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140548556,"id":"rs1796995653","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1378567412","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140548558,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548558,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1332549133","source":"dbSNP","start":140548562,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140548562,"alleles":["C","T"],"feature_type":"variation","strand":1},{"start":140548564,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140548564,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs551115064","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548575,"feature_type":"variation","strand":1,"end":140548575,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs985511035"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548576,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140548576,"clinical_significance":[],"seq_region_name":"7","id":"rs1796996170"},{"end":140548580,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140548580,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1796996276"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796996383","feature_type":"variation","strand":1,"end":140548585,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548585},{"clinical_significance":[],"seq_region_name":"7","id":"rs1489060014","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548587,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140548587},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548588,"feature_type":"variation","strand":1,"end":140548588,"alleles":["T","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs983506238"},{"seq_region_name":"7","id":"rs1796996699","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140548598,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548598,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1796996801","alleles":["A","G"],"end":140548599,"feature_type":"variation","strand":1,"source":"dbSNP","start":140548599,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1196687461","clinical_significance":[],"start":140548600,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140548600,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"id":"rs986159657","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140548602,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548602,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1236960702","clinical_significance":[],"end":140548608,"alleles":["TTTTTTT","TTTTTTTT"],"strand":1,"feature_type":"variation","start":140548602,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1368660552","clinical_significance":[],"alleles":["T","C"],"end":140548605,"strand":1,"feature_type":"variation","start":140548605,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140548610,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548610,"source":"dbSNP","seq_region_name":"7","id":"rs1796997358","clinical_significance":[]},{"alleles":["T","A"],"end":140548612,"strand":1,"feature_type":"variation","start":140548612,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs563141663","clinical_significance":[]},{"alleles":["A","T"],"end":140548614,"feature_type":"variation","strand":1,"source":"dbSNP","start":140548614,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130534710"},{"source":"dbSNP","start":140548615,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TTTTTT","TTTTTTT","TTTTTTTT"],"end":140548620,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1461372770"},{"start":140548619,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140548619,"alleles":["T","G"],"strand":1,"feature_type":"variation","id":"rs1796997698","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1796997801","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548620,"source":"dbSNP","strand":1,"feature_type":"variation","end":140548619,"alleles":["-","AA"]},{"source":"dbSNP","start":140548621,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140548621,"alleles":["A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1459025079"},{"strand":1,"feature_type":"variation","end":140548630,"alleles":["TTTTTTTTT","TTTTTTTT","TTTTTTTTTT","TTTTTTTTTTT","TTTTTTTTTTTT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548622,"source":"dbSNP","seq_region_name":"7","id":"rs552050748","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140548631,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548631,"source":"dbSNP","id":"rs1197747562","seq_region_name":"7","clinical_significance":[]},{"end":140548634,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140548634,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1488714911","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548635,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140548635,"clinical_significance":[],"seq_region_name":"7","id":"rs1796998435"},{"seq_region_name":"7","id":"rs1014920796","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140548637,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548637,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1240856347","seq_region_name":"7","source":"dbSNP","start":140548643,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140548643,"alleles":["C","G","T"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140548644,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140548644,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1422917571"},{"alleles":["C","T"],"end":140548645,"feature_type":"variation","strand":1,"source":"dbSNP","start":140548645,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1310057276"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140548654,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548654,"source":"dbSNP","seq_region_name":"7","id":"rs1242486874","clinical_significance":[]},{"id":"rs1796999096","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140548658,"strand":1,"feature_type":"variation","start":140548658,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548660,"feature_type":"variation","strand":1,"end":140548660,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1164473415"},{"end":140548665,"alleles":["GGGG","GGG"],"strand":1,"feature_type":"variation","start":140548662,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1374019563","clinical_significance":[]},{"alleles":["G","C"],"end":140548663,"strand":1,"feature_type":"variation","start":140548663,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1796999383","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs915277066","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548664,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140548664},{"end":140548665,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140548665,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs966257384"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548666,"feature_type":"variation","strand":1,"end":140548666,"alleles":["T","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs976630538"},{"end":140548668,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140548668,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs374446453","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1393367327","end":140548670,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140548670,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140548672,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140548672,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1797000029","seq_region_name":"7"},{"source":"dbSNP","start":140548675,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140548675,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1463930286"},{"clinical_significance":[],"id":"rs2130534937","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548675,"feature_type":"variation","strand":1,"end":140548676,"alleles":["AT","-"]},{"id":"rs2130534950","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140548677,"alleles":["-","CA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548678,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1797000265","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548678,"source":"dbSNP","strand":1,"feature_type":"variation","end":140548678,"alleles":["A","T"]},{"clinical_significance":[],"id":"rs530953582","seq_region_name":"7","alleles":["C","T"],"end":140548682,"feature_type":"variation","strand":1,"source":"dbSNP","start":140548682,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548683,"source":"dbSNP","strand":1,"feature_type":"variation","end":140548683,"alleles":["G","A"],"id":"rs1169173403","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140548685,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548685,"source":"dbSNP","id":"rs1400298281","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1797000702","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548689,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140548689},{"id":"rs1797000793","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548691,"source":"dbSNP","strand":1,"feature_type":"variation","end":140548691,"alleles":["G","T"]},{"alleles":["C","A"],"end":140548695,"strand":1,"feature_type":"variation","start":140548695,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs922239632","seq_region_name":"7","clinical_significance":[]},{"end":140548696,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140548696,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1470338285"},{"source":"dbSNP","start":140548701,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140548701,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1797001085","seq_region_name":"7"},{"end":140548704,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140548704,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs953740299"},{"clinical_significance":[],"seq_region_name":"7","id":"rs946940573","end":140548705,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140548705,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140548706,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C","G"],"end":140548706,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1378384261","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548707,"feature_type":"variation","strand":1,"end":140548707,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1177964578"},{"clinical_significance":[],"id":"rs985164818","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548709,"feature_type":"variation","strand":1,"end":140548709,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130535090","end":140548711,"alleles":["GTT","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140548709,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1585602550","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548710,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140548710},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797001958","end":140548712,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140548712,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs978664212","clinical_significance":[],"alleles":["T","C"],"end":140548720,"strand":1,"feature_type":"variation","start":140548720,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1585602570","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548722,"source":"dbSNP","strand":1,"feature_type":"variation","end":140548722,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1338839322","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548723,"feature_type":"variation","strand":1,"end":140548723,"alleles":["C","A"]},{"alleles":["C","A"],"end":140548724,"feature_type":"variation","strand":1,"source":"dbSNP","start":140548724,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130535140"},{"end":140548726,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140548726,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797002392","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797002486","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140548728,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548728,"source":"dbSNP"},{"start":140548737,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140548737,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs549052577","clinical_significance":[]},{"alleles":["C","T"],"end":140548738,"strand":1,"feature_type":"variation","start":140548738,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1395692543","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140548739,"alleles":["G","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548739,"clinical_significance":[],"seq_region_name":"7","id":"rs761652250"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1351625510","source":"dbSNP","start":140548741,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140548741,"feature_type":"variation","strand":1},{"start":140548749,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140548749,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130535214","clinical_significance":[]},{"source":"dbSNP","start":140548751,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140548751,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797003072"},{"clinical_significance":[],"seq_region_name":"7","id":"rs567682208","alleles":["C","T"],"end":140548754,"feature_type":"variation","strand":1,"source":"dbSNP","start":140548754,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548759,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140548759,"clinical_significance":[],"seq_region_name":"7","id":"rs894834647"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548760,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140548760,"seq_region_name":"7","id":"rs1797003384","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548763,"source":"dbSNP","strand":1,"feature_type":"variation","end":140548763,"alleles":["A","G"],"seq_region_name":"7","id":"rs947664786","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140548764,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548764,"clinical_significance":[],"seq_region_name":"7","id":"rs1048813153"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140548767,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548767,"source":"dbSNP","seq_region_name":"7","id":"rs1257327475","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130535288","clinical_significance":[],"alleles":["C","T"],"end":140548768,"strand":1,"feature_type":"variation","start":140548768,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140548770,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548770,"source":"dbSNP","id":"rs528450978","seq_region_name":"7","clinical_significance":[]},{"end":140548773,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140548773,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs935619072","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140548774,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548774,"clinical_significance":[],"seq_region_name":"7","id":"rs1797004039"},{"feature_type":"variation","strand":1,"end":140548776,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548776,"clinical_significance":[],"seq_region_name":"7","id":"rs1797004150"},{"id":"rs1298487573","seq_region_name":"7","clinical_significance":[],"start":140548786,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140548786,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1004741640","end":140548788,"alleles":["G","C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140548788,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140548789,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548789,"source":"dbSNP","seq_region_name":"7","id":"rs1797004510","clinical_significance":[]},{"end":140548794,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140548794,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1797004601","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140548795,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548795,"clinical_significance":[],"seq_region_name":"7","id":"rs1797004702"},{"seq_region_name":"7","id":"rs1797004801","clinical_significance":[],"end":140548800,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140548800,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140548801,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548801,"clinical_significance":[],"seq_region_name":"7","id":"rs1324249379"},{"seq_region_name":"7","id":"rs575552237","clinical_significance":[],"start":140548802,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140548802,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1358113932","clinical_significance":[],"start":140548802,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140548805,"alleles":["GGGG","GGG"],"strand":1,"feature_type":"variation"},{"start":140548804,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140548804,"strand":1,"feature_type":"variation","id":"rs1036589285","seq_region_name":"7","clinical_significance":[]},{"end":140548806,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140548806,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585602730","clinical_significance":[]},{"alleles":["A","-"],"end":140548813,"strand":1,"feature_type":"variation","start":140548813,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1052873971","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1379364580","clinical_significance":[],"start":140548813,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140548813,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140548814,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548814,"clinical_significance":[],"seq_region_name":"7","id":"rs1196438372"},{"clinical_significance":[],"seq_region_name":"7","id":"rs901653643","end":140548818,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140548818,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["G","C","T"],"end":140548819,"feature_type":"variation","strand":1,"source":"dbSNP","start":140548819,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1264109276"},{"end":140548824,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140548824,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs997406576"},{"seq_region_name":"7","id":"rs1253774337","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140548828,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548828,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1487311070","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140548832,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548832,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1285414832","clinical_significance":[],"alleles":["G","A"],"end":140548833,"strand":1,"feature_type":"variation","start":140548833,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140548840,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140548840,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1201166844"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140548841,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548841,"clinical_significance":[],"seq_region_name":"7","id":"rs1028827260"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1254806395","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548843,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140548843},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548844,"feature_type":"variation","strand":1,"end":140548844,"alleles":["C","A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1045954661"},{"seq_region_name":"7","id":"rs1262790466","clinical_significance":[],"end":140548848,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140548848,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1797006954","clinical_significance":[],"start":140548849,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140548849,"strand":1,"feature_type":"variation"},{"id":"rs1430660292","seq_region_name":"7","clinical_significance":[],"start":140548851,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140548851,"alleles":["G","A","C"],"strand":1,"feature_type":"variation"},{"id":"rs1401472792","seq_region_name":"7","clinical_significance":[],"alleles":["T","A"],"end":140548853,"strand":1,"feature_type":"variation","start":140548853,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs905817401","source":"dbSNP","start":140548854,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140548854,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs72611557","seq_region_name":"7","source":"dbSNP","start":140548857,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140548857,"alleles":["C","T"],"feature_type":"variation","strand":1},{"alleles":["C","G"],"end":140548859,"feature_type":"variation","strand":1,"source":"dbSNP","start":140548859,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797007506"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140548860,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548860,"source":"dbSNP","seq_region_name":"7","id":"rs1048929347","clinical_significance":[]},{"alleles":["C","T"],"end":140548861,"strand":1,"feature_type":"variation","start":140548861,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1481074385","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1414581726","clinical_significance":[],"start":140548862,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140548862,"strand":1,"feature_type":"variation"},{"start":140548864,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140548864,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs887778831","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140548865,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548865,"source":"dbSNP","id":"rs1178615326","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1424077016","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548867,"feature_type":"variation","strand":1,"end":140548867,"alleles":["C","G"]},{"alleles":["A","AAA"],"end":140548873,"feature_type":"variation","strand":1,"source":"dbSNP","start":140548873,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797008014"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1173021683","alleles":["G","A"],"end":140548874,"feature_type":"variation","strand":1,"source":"dbSNP","start":140548874,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548876,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140548876,"seq_region_name":"7","id":"rs1797008213","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548877,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140548877,"seq_region_name":"7","id":"rs1797008352","clinical_significance":[]},{"source":"dbSNP","start":140548880,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140548880,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797008459"},{"seq_region_name":"7","id":"rs1357513948","clinical_significance":[],"alleles":["G","A","C","T"],"end":140548881,"strand":1,"feature_type":"variation","start":140548881,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130535683","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548882,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140548882},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797008707","source":"dbSNP","start":140548884,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140548884,"alleles":["T","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1465670923","seq_region_name":"7","source":"dbSNP","start":140548891,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140548891,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs188313268","alleles":["G","A"],"end":140548893,"feature_type":"variation","strand":1,"source":"dbSNP","start":140548893,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140548895,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140548895,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797009051"},{"source":"dbSNP","start":140548896,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140548896,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1022417983"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548897,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140548897,"clinical_significance":[],"seq_region_name":"7","id":"rs968520414"},{"seq_region_name":"7","id":"rs997719966","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548898,"source":"dbSNP","strand":1,"feature_type":"variation","end":140548898,"alleles":["A","G"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548917,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140548917,"seq_region_name":"7","id":"rs1318961448","clinical_significance":[]},{"alleles":["T","C"],"end":140548918,"feature_type":"variation","strand":1,"source":"dbSNP","start":140548918,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1029573850"},{"feature_type":"variation","strand":1,"end":140548919,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548919,"clinical_significance":[],"id":"rs191395490","seq_region_name":"7"},{"source":"dbSNP","start":140548926,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140548926,"alleles":["T","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1315645442","seq_region_name":"7"},{"alleles":["G","A","T"],"end":140548927,"feature_type":"variation","strand":1,"source":"dbSNP","start":140548927,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797009912"},{"alleles":["A","G"],"end":140548932,"strand":1,"feature_type":"variation","start":140548932,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797010032","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs953688845","source":"dbSNP","start":140548933,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140548933,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1585603133","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548934,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140548934},{"seq_region_name":"7","id":"rs1269278166","clinical_significance":[],"alleles":["C","G"],"end":140548935,"strand":1,"feature_type":"variation","start":140548935,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585603159","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548938,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140548938},{"source":"dbSNP","start":140548940,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140548940,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs557626330","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140548941,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548941,"source":"dbSNP","seq_region_name":"7","id":"rs1277368388","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140548942,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548942,"clinical_significance":[],"id":"rs1341777178","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140548946,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548946,"source":"dbSNP","seq_region_name":"7","id":"rs1797010896","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140548956,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548956,"clinical_significance":[],"seq_region_name":"7","id":"rs1332032663"},{"source":"dbSNP","start":140548963,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140548963,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1451839910","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs183850826","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548964,"feature_type":"variation","strand":1,"end":140548964,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797011329","end":140548965,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140548965,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797011429","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140548966,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548966},{"seq_region_name":"7","id":"rs537171119","clinical_significance":[],"strand":1,"feature_type":"variation","end":140548967,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548967,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548973,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140548973,"clinical_significance":[],"seq_region_name":"7","id":"rs1797011697"},{"start":140548976,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140548976,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130535926","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130535934","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140548977,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548977},{"seq_region_name":"7","id":"rs1172550405","clinical_significance":[],"strand":1,"feature_type":"variation","end":140548978,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548978,"source":"dbSNP"},{"start":140548979,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140548979,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130535950","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548981,"feature_type":"variation","strand":1,"end":140548981,"alleles":["G","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1463906704"},{"alleles":["C","G"],"end":140548983,"strand":1,"feature_type":"variation","start":140548983,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs2130535971","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140548987,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548987,"clinical_significance":[],"seq_region_name":"7","id":"rs992415446"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548988,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140548988,"id":"rs2130535988","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1298491274","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548989,"source":"dbSNP","strand":1,"feature_type":"variation","end":140548989,"alleles":["C","T"]},{"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140548990,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548990,"source":"dbSNP","seq_region_name":"7","id":"rs2130536003","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140548992,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140548992,"source":"dbSNP","seq_region_name":"7","id":"rs2130536015","clinical_significance":[]},{"start":140548993,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","T"],"end":140548993,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs916802811","clinical_significance":[]},{"end":140548994,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140548994,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs947739317"},{"id":"rs1473796889","seq_region_name":"7","clinical_significance":[],"end":140548995,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140548995,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140548997,"feature_type":"variation","strand":1,"end":140548997,"alleles":["T","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1049184608"},{"id":"rs1311111117","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140549000,"strand":1,"feature_type":"variation","start":140549000,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1797012835","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549005,"source":"dbSNP","strand":1,"feature_type":"variation","end":140549005,"alleles":["G","A"]},{"alleles":["G","C"],"end":140549010,"strand":1,"feature_type":"variation","start":140549010,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1797012940","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797013048","clinical_significance":[],"alleles":["G","C"],"end":140549017,"strand":1,"feature_type":"variation","start":140549017,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549018,"source":"dbSNP","strand":1,"feature_type":"variation","end":140549018,"alleles":["A","G"],"id":"rs1183461418","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585603380","clinical_significance":[],"end":140549020,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140549020,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140549024,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549024,"clinical_significance":[],"seq_region_name":"7","id":"rs565460463"},{"seq_region_name":"7","id":"rs1797013467","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549028,"source":"dbSNP","strand":1,"feature_type":"variation","end":140549028,"alleles":["G","GG"]},{"id":"rs187733122","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549029,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140549029},{"clinical_significance":[],"id":"rs1797013720","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549033,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140549033},{"clinical_significance":[],"seq_region_name":"7","id":"rs940447116","feature_type":"variation","strand":1,"end":140549035,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549035},{"clinical_significance":[],"seq_region_name":"7","id":"rs1036088950","feature_type":"variation","strand":1,"end":140549036,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549036},{"clinical_significance":[],"id":"rs1585603452","seq_region_name":"7","source":"dbSNP","start":140549038,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140549038,"alleles":["T","G"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549039,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140549039,"clinical_significance":[],"seq_region_name":"7","id":"rs901686479"},{"clinical_significance":[],"id":"rs958182443","seq_region_name":"7","end":140549042,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140549042,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs192647520","seq_region_name":"7","clinical_significance":[],"end":140549043,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140549043,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140549047,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549047,"source":"dbSNP","seq_region_name":"7","id":"rs1357779753","clinical_significance":[]},{"seq_region_name":"7","id":"rs540630099","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549048,"source":"dbSNP","strand":1,"feature_type":"variation","end":140549048,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1797014763","clinical_significance":[],"start":140549051,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140549051,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs2130536243","clinical_significance":[],"alleles":["C","T"],"end":140549054,"strand":1,"feature_type":"variation","start":140549054,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797014859","alleles":["T","C"],"end":140549055,"feature_type":"variation","strand":1,"source":"dbSNP","start":140549055,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1423763978","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549058,"source":"dbSNP","strand":1,"feature_type":"variation","end":140549058,"alleles":["A","G"]},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140549060,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549060,"source":"dbSNP","seq_region_name":"7","id":"rs1797015082","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140549063,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549063,"source":"dbSNP","seq_region_name":"7","id":"rs1244656198","clinical_significance":[]},{"source":"dbSNP","start":140549073,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140549073,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1377548308","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140549074,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549074,"clinical_significance":[],"seq_region_name":"7","id":"rs1797015362"},{"feature_type":"variation","strand":1,"end":140549076,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549076,"clinical_significance":[],"seq_region_name":"7","id":"rs1797015466"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549077,"feature_type":"variation","strand":1,"end":140549077,"alleles":["C","T"],"clinical_significance":[],"id":"rs889030956","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1006917507","feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140549078,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549078},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549079,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140549079,"seq_region_name":"7","id":"rs1353710388","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549083,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140549083,"clinical_significance":[],"id":"rs553236934","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1022705286","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140549085,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549085,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs968048311","end":140549086,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140549086,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1163008551","seq_region_name":"7","clinical_significance":[],"end":140549088,"alleles":["GG","G"],"strand":1,"feature_type":"variation","start":140549087,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1048982548","alleles":["G","A"],"end":140549088,"feature_type":"variation","strand":1,"source":"dbSNP","start":140549088,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140549115,"alleles":["TATATTCCCAGATATATTCCCAGATA","TATATTCCCAGATA"],"strand":1,"feature_type":"variation","start":140549090,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797016435","clinical_significance":[]},{"id":"rs1418128603","seq_region_name":"7","clinical_significance":[],"alleles":["A","T"],"end":140549093,"strand":1,"feature_type":"variation","start":140549093,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1297304621","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140549094,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549094,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1177321256","feature_type":"variation","strand":1,"end":140549095,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549095},{"alleles":["C","A"],"end":140549096,"strand":1,"feature_type":"variation","start":140549096,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1797016924","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549103,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140549103,"id":"rs1469912536","seq_region_name":"7","clinical_significance":[]},{"start":140549107,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140549107,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797017142","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549108,"feature_type":"variation","strand":1,"end":140549108,"alleles":["C","G"],"clinical_significance":[],"id":"rs1797017250","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1797017364","clinical_significance":[],"start":140549117,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140549117,"alleles":["A","C","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797017519","end":140549118,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140549118,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140549120,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549120,"clinical_significance":[],"seq_region_name":"7","id":"rs1247679938"},{"end":140549122,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140549122,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797017768","clinical_significance":[]},{"seq_region_name":"7","id":"rs1365980583","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549126,"source":"dbSNP","strand":1,"feature_type":"variation","end":140549126,"alleles":["T","G"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549127,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140549127,"seq_region_name":"7","id":"rs1797018026","clinical_significance":[]},{"seq_region_name":"7","id":"rs1406627583","clinical_significance":[],"strand":1,"feature_type":"variation","end":140549138,"alleles":["AGAAGAA","AGAA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549132,"source":"dbSNP"},{"start":140549133,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140549133,"alleles":["G","GG"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797018275","clinical_significance":[]},{"clinical_significance":[],"id":"rs1797018393","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549139,"feature_type":"variation","strand":1,"end":140549139,"alleles":["T","A"]},{"alleles":["T","C"],"end":140549144,"feature_type":"variation","strand":1,"source":"dbSNP","start":140549144,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1797018492","seq_region_name":"7"},{"id":"rs1797018601","seq_region_name":"7","clinical_significance":[],"start":140549149,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140549149,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549156,"source":"dbSNP","strand":1,"feature_type":"variation","end":140549156,"alleles":["G","A"],"seq_region_name":"7","id":"rs1224304184","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549163,"feature_type":"variation","strand":1,"end":140549163,"alleles":["T","C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585603722"},{"id":"rs1563132673","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549164,"source":"dbSNP","strand":1,"feature_type":"variation","end":140549164,"alleles":["T","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797019089","alleles":["T","G"],"end":140549166,"feature_type":"variation","strand":1,"source":"dbSNP","start":140549166,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140549170,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140549170,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797019206","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549173,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140549173,"seq_region_name":"7","id":"rs1585603738","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140549174,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549174,"clinical_significance":[],"seq_region_name":"7","id":"rs60165201"},{"end":140549176,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140549176,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585603758","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797019639","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549177,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140549177},{"feature_type":"variation","strand":1,"end":140549180,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549180,"clinical_significance":[],"seq_region_name":"7","id":"rs10267752"},{"clinical_significance":[],"id":"rs544894321","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549181,"feature_type":"variation","strand":1,"end":140549181,"alleles":["G","A"]},{"end":140549182,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140549182,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1036755985","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1308567377","end":140549183,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140549183,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140549185,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140549185,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1311280461","clinical_significance":[]},{"end":140549186,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140549186,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1237905248","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1797020483","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549187,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140549187},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549190,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140549190,"seq_region_name":"7","id":"rs1797020590","clinical_significance":[]},{"end":140549191,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","start":140549191,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1585603831","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140549194,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549194,"source":"dbSNP","seq_region_name":"7","id":"rs1797020834","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549195,"feature_type":"variation","strand":1,"end":140549195,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1797020955"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549201,"feature_type":"variation","strand":1,"end":140549201,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1372277890"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1351000657","feature_type":"variation","strand":1,"end":140549203,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549203},{"end":140549204,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140549204,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs2130536694","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797021209","end":140549207,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140549207,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs879847166","feature_type":"variation","strand":1,"end":140549208,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549208},{"alleles":["A","G"],"end":140549215,"feature_type":"variation","strand":1,"source":"dbSNP","start":140549215,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797021429"},{"start":140549218,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140549218,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1238990681","clinical_significance":[]},{"source":"dbSNP","start":140549221,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140549221,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1490613718"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1438434143","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549223,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140549223},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140549224,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549224,"source":"dbSNP","seq_region_name":"7","id":"rs1797021919","clinical_significance":[]},{"start":140549224,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AAAAAAAAAAA","AAAAAAAAA","AAAAAAAAAA","AAAAAAAAAAAA"],"end":140549234,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs200550587","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549227,"feature_type":"variation","strand":1,"end":140549227,"alleles":["A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1797022280"},{"seq_region_name":"7","id":"rs1362573323","clinical_significance":[],"strand":1,"feature_type":"variation","end":140549231,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549231,"source":"dbSNP"},{"source":"dbSNP","start":140549233,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140549233,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1157332402"},{"strand":1,"feature_type":"variation","end":140549234,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549234,"source":"dbSNP","seq_region_name":"7","id":"rs1400615311","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140549235,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549235,"clinical_significance":[],"seq_region_name":"7","id":"rs1797022774"},{"seq_region_name":"7","id":"rs1797022897","clinical_significance":[],"start":140549244,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140549244,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1031055116","seq_region_name":"7","feature_type":"variation","strand":1,"end":140549248,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549248},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797023133","alleles":["T","C"],"end":140549249,"feature_type":"variation","strand":1,"source":"dbSNP","start":140549249,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1204578642","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549261,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140549261},{"seq_region_name":"7","id":"rs1797023348","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","AA"],"end":140549263,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549263,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1797023478","clinical_significance":[],"start":140549264,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140549264,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140549266,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549266,"source":"dbSNP","seq_region_name":"7","id":"rs1797023598","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs563178925","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549267,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140549267},{"alleles":["T","C"],"end":140549268,"strand":1,"feature_type":"variation","start":140549268,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797023848","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140549277,"alleles":["TTTTTTTTTT","TTTTTTTTT","TTTTTTTTTTT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549268,"clinical_significance":[],"seq_region_name":"7","id":"rs368879127"},{"seq_region_name":"7","id":"rs140145608","clinical_significance":[],"start":140549271,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140549271,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585604041","end":140549276,"alleles":["-","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140549277,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140549277,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140549277,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1177807888"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1287566662","feature_type":"variation","strand":1,"end":140549278,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549278},{"seq_region_name":"7","id":"rs1797024629","clinical_significance":[],"end":140549280,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140549280,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs543132528","clinical_significance":[],"start":140549286,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140549286,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140549287,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549287,"source":"dbSNP","id":"rs752922255","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1213088710","clinical_significance":[],"strand":1,"feature_type":"variation","end":140549293,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549293,"source":"dbSNP"},{"start":140549299,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140549299,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1316235313","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140549300,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549300,"source":"dbSNP","id":"rs1240124491","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140549303,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549303,"clinical_significance":[],"id":"rs960874093","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140549307,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549307,"clinical_significance":[],"id":"rs60565138","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549313,"feature_type":"variation","strand":1,"end":140549313,"alleles":["T","C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585604145"},{"source":"dbSNP","start":140549316,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140549316,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797025696"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140549317,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549317,"clinical_significance":[],"seq_region_name":"7","id":"rs1797025821"},{"source":"dbSNP","start":140549318,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140549318,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585604163"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549321,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140549321,"clinical_significance":[],"seq_region_name":"7","id":"rs561181730"},{"clinical_significance":[],"seq_region_name":"7","id":"rs528486869","source":"dbSNP","start":140549322,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140549322,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs988514823","source":"dbSNP","start":140549324,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140549324,"alleles":["A","G"],"feature_type":"variation","strand":1},{"start":140549325,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140549325,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1563132810","clinical_significance":[]},{"alleles":["T","C"],"end":140549333,"strand":1,"feature_type":"variation","start":140549333,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130537060","clinical_significance":[]},{"seq_region_name":"7","id":"rs916856891","clinical_significance":[],"end":140549335,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140549335,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797026607","source":"dbSNP","start":140549339,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140549339,"alleles":["C","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1296386035","end":140549340,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140549340,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs796152412","seq_region_name":"7","source":"dbSNP","start":140549347,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140549347,"alleles":["G","C"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549351,"feature_type":"variation","strand":1,"end":140549351,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs985029093"},{"seq_region_name":"7","id":"rs1386174766","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549354,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140549354},{"seq_region_name":"7","id":"rs1797027124","clinical_significance":[],"start":140549355,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140549355,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797027236","source":"dbSNP","start":140549356,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140549356,"alleles":["C","A"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140549357,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549357,"source":"dbSNP","id":"rs1797027350","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1645339038","seq_region_name":"7","alleles":["G","C"],"end":140549359,"feature_type":"variation","strand":1,"source":"dbSNP","start":140549359,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797027464","end":140549363,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140549363,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140549368,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549368,"source":"dbSNP","seq_region_name":"7","id":"rs1426304727","clinical_significance":[]},{"alleles":["G","C"],"end":140549376,"feature_type":"variation","strand":1,"source":"dbSNP","start":140549376,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797027665"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797027776","alleles":["CCTCC","CC"],"end":140549381,"feature_type":"variation","strand":1,"source":"dbSNP","start":140549377,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs546722351","source":"dbSNP","start":140549378,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140549378,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs908887916","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549381,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140549381},{"strand":1,"feature_type":"variation","end":140549382,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549382,"source":"dbSNP","seq_region_name":"7","id":"rs1162491954","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797028205","source":"dbSNP","start":140549383,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140549383,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549384,"source":"dbSNP","strand":1,"feature_type":"variation","end":140549384,"alleles":["A","G"],"id":"rs1797028320","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140549391,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140549391,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1429060298"},{"end":140549400,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140549400,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1175200133"},{"seq_region_name":"7","id":"rs1797028660","clinical_significance":[],"start":140549404,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140549404,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"alleles":["G","T"],"end":140549405,"strand":1,"feature_type":"variation","start":140549405,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1477928919","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797028880","feature_type":"variation","strand":1,"end":140549407,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549407},{"end":140549409,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140549409,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1264927010","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797029125","clinical_significance":[],"start":140549411,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140549411,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1797029223","clinical_significance":[],"alleles":["C","T"],"end":140549414,"strand":1,"feature_type":"variation","start":140549414,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1797029322","clinical_significance":[],"end":140549418,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140549418,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140549423,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549423,"source":"dbSNP","seq_region_name":"7","id":"rs1797029442","clinical_significance":[]},{"start":140549427,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140549427,"alleles":["C","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797029541","clinical_significance":[]},{"source":"dbSNP","start":140549437,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140549437,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1797029665","seq_region_name":"7"},{"start":140549438,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140549438,"alleles":["A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797029760","clinical_significance":[]},{"alleles":["G","A"],"end":140549439,"strand":1,"feature_type":"variation","start":140549439,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797029866","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549440,"source":"dbSNP","strand":1,"feature_type":"variation","end":140549440,"alleles":["T","G"],"seq_region_name":"7","id":"rs1797029970","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797030067","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140549441,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549441,"source":"dbSNP"},{"seq_region_name":"7","id":"rs940328856","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549442,"source":"dbSNP","strand":1,"feature_type":"variation","end":140549442,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797030284","source":"dbSNP","start":140549443,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140549443,"alleles":["A","G"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549446,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140549446,"seq_region_name":"7","id":"rs1036528829","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs571605336","end":140549447,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140549447,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1237920822","clinical_significance":[],"strand":1,"feature_type":"variation","end":140549451,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549451,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140549457,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549457,"clinical_significance":[],"seq_region_name":"7","id":"rs1797030825"},{"strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140549458,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549458,"source":"dbSNP","seq_region_name":"7","id":"rs1212196353","clinical_significance":[]},{"id":"rs1797031148","seq_region_name":"7","clinical_significance":[],"start":140549459,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140549459,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"alleles":["G","A"],"end":140549460,"strand":1,"feature_type":"variation","start":140549460,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797031252","clinical_significance":[]},{"source":"dbSNP","start":140549469,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140549469,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797031365"},{"alleles":["T","C"],"end":140549471,"feature_type":"variation","strand":1,"source":"dbSNP","start":140549471,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1262255303","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549476,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140549476,"clinical_significance":[],"seq_region_name":"7","id":"rs1797031589"},{"seq_region_name":"7","id":"rs1442876776","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140549483,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549483,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130537460","source":"dbSNP","start":140549487,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140549487,"alleles":["A","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797031836","feature_type":"variation","strand":1,"end":140549488,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549488},{"id":"rs1299339602","seq_region_name":"7","clinical_significance":[],"alleles":["C","G","T"],"end":140549490,"strand":1,"feature_type":"variation","start":140549490,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs140626900","seq_region_name":"7","clinical_significance":[],"start":140549491,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140549491,"strand":1,"feature_type":"variation"},{"id":"rs1445485778","seq_region_name":"7","clinical_significance":[],"alleles":["C","A","T"],"end":140549498,"strand":1,"feature_type":"variation","start":140549498,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["CC","C"],"end":140549502,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549501,"source":"dbSNP","seq_region_name":"7","id":"rs1797032396","clinical_significance":[]},{"source":"dbSNP","start":140549504,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140549504,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs933193319"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549505,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140549505,"clinical_significance":[],"seq_region_name":"7","id":"rs35378830"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797032810","feature_type":"variation","strand":1,"end":140549512,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549512},{"seq_region_name":"7","id":"rs1379988757","clinical_significance":[],"end":140549517,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140549517,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1305066762","clinical_significance":[],"alleles":["G","C"],"end":140549518,"strand":1,"feature_type":"variation","start":140549518,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140549520,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140549520,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1797033000","seq_region_name":"7"},{"id":"rs368341269","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140549521,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549521,"source":"dbSNP"},{"start":140549531,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140549531,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1406051254","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549535,"feature_type":"variation","strand":1,"end":140549535,"alleles":["A","G"],"clinical_significance":[],"id":"rs2130537592","seq_region_name":"7"},{"alleles":["G","A"],"end":140549537,"strand":1,"feature_type":"variation","start":140549537,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs947305727","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1288203884","seq_region_name":"7","source":"dbSNP","start":140549539,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140549539,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1467571379","seq_region_name":"7","end":140549540,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140549540,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549544,"feature_type":"variation","strand":1,"end":140549544,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs984577962"},{"source":"dbSNP","start":140549545,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140549545,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797033779"},{"source":"dbSNP","start":140549546,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140549546,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797033893"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797033989","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549546,"feature_type":"variation","strand":1,"end":140549548,"alleles":["CCC","CC"]},{"end":140549548,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140549548,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs767759301","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140549549,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549549,"clinical_significance":[],"seq_region_name":"7","id":"rs1042955870"},{"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140549555,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549555,"source":"dbSNP","seq_region_name":"7","id":"rs1797034390","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs940611177","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549556,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140549556},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549557,"source":"dbSNP","strand":1,"feature_type":"variation","end":140549559,"alleles":["AAA","AA"],"seq_region_name":"7","id":"rs1797034647","clinical_significance":[]},{"id":"rs1797034750","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549560,"source":"dbSNP","strand":1,"feature_type":"variation","end":140549560,"alleles":["T","C"]},{"source":"dbSNP","start":140549562,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140549562,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1183148410"},{"feature_type":"variation","strand":1,"alleles":["AATTAAT","AAT"],"end":140549571,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549565,"clinical_significance":[],"seq_region_name":"7","id":"rs1036400260"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549566,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140549566,"id":"rs115545792","seq_region_name":"7","clinical_significance":[]},{"alleles":["TT","T"],"end":140549568,"strand":1,"feature_type":"variation","start":140549567,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1199023285","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1243953844","feature_type":"variation","strand":1,"end":140549568,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549568},{"start":140549569,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140549569,"strand":1,"feature_type":"variation","id":"rs1797035324","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549570,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140549570,"clinical_significance":[],"seq_region_name":"7","id":"rs1473921831"},{"seq_region_name":"7","id":"rs1797035553","clinical_significance":[],"end":140549571,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140549571,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs536807221","seq_region_name":"7","feature_type":"variation","strand":1,"end":140549574,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549574},{"alleles":["A","C"],"end":140549579,"strand":1,"feature_type":"variation","start":140549579,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1797035803","seq_region_name":"7","clinical_significance":[]},{"start":140549582,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140549582,"strand":1,"feature_type":"variation","id":"rs1797035912","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","-"],"end":140549591,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549591,"clinical_significance":[],"seq_region_name":"7","id":"rs1227004775"},{"source":"dbSNP","start":140549591,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140549591,"alleles":["A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797036015"},{"end":140549592,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140549592,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1050961789","clinical_significance":[]},{"id":"rs201134540","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549592,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TTTTTTT","TTTTTT"],"end":140549598},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797036500","source":"dbSNP","start":140549593,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140549593,"feature_type":"variation","strand":1},{"start":140549599,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140549598,"alleles":["-","G"],"strand":1,"feature_type":"variation","id":"rs1797036609","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140549601,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140549601,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1585604655","seq_region_name":"7"},{"start":140549605,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140549605,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs889190361","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130537867","clinical_significance":[],"end":140549606,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140549606,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797036976","source":"dbSNP","start":140549607,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140549607,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140549609,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549609,"clinical_significance":[],"seq_region_name":"7","id":"rs1246427532"},{"seq_region_name":"7","id":"rs1797037201","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140549610,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549610,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140549611,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549611,"clinical_significance":[],"seq_region_name":"7","id":"rs1797037309"},{"id":"rs1310651218","seq_region_name":"7","clinical_significance":[],"start":140549612,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140549612,"alleles":["T","G"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549615,"source":"dbSNP","strand":1,"feature_type":"variation","end":140549615,"alleles":["T","C"],"seq_region_name":"7","id":"rs1797037520","clinical_significance":[]},{"alleles":["A","C"],"end":140549626,"feature_type":"variation","strand":1,"source":"dbSNP","start":140549626,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1797037627","seq_region_name":"7"},{"end":140549627,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","start":140549627,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1449379771","clinical_significance":[]},{"id":"rs1797038079","seq_region_name":"7","clinical_significance":[],"end":140549629,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140549629,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549630,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TTTT","TTT"],"end":140549633,"id":"rs1797038255","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549633,"feature_type":"variation","strand":1,"end":140549633,"alleles":["T","C"],"clinical_significance":[],"id":"rs1797038440","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1394825706","seq_region_name":"7","feature_type":"variation","strand":1,"end":140549634,"alleles":["G","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549634},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130537962","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140549636,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549636},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140549639,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549639,"clinical_significance":[],"id":"rs1797038850","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1031128171","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549641,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140549641},{"clinical_significance":[],"seq_region_name":"7","id":"rs896552196","end":140549645,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140549645,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["TAAATAAA","TAAA"],"end":140549654,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549647,"source":"dbSNP","seq_region_name":"7","id":"rs1797039396","clinical_significance":[]},{"alleles":["T","A"],"end":140549656,"strand":1,"feature_type":"variation","start":140549656,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1650752861","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["TTATTATTA","TTATTA"],"end":140549665,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549657,"clinical_significance":[],"seq_region_name":"7","id":"rs1296045502"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140549663,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549663,"source":"dbSNP","seq_region_name":"7","id":"rs1797039747","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1013788420","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549664,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140549664},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549671,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140549671,"clinical_significance":[],"seq_region_name":"7","id":"rs543834779"},{"id":"rs1032508287","seq_region_name":"7","clinical_significance":[],"start":140549673,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140549673,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs2130538053","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549676,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140549676},{"start":140549678,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140549678,"strand":1,"feature_type":"variation","id":"rs1585604751","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1023820208","feature_type":"variation","strand":1,"end":140549683,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549683},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797040871","alleles":["G","A"],"end":140549685,"feature_type":"variation","strand":1,"source":"dbSNP","start":140549685,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1442304076","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549687,"source":"dbSNP","strand":1,"feature_type":"variation","end":140549687,"alleles":["A","C"]},{"alleles":["G","C"],"end":140549688,"feature_type":"variation","strand":1,"source":"dbSNP","start":140549688,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs373218980"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549694,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140549694,"seq_region_name":"7","id":"rs1384486545","clinical_significance":[]},{"id":"rs1797041602","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140549696,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549696,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549701,"feature_type":"variation","strand":1,"alleles":["C","-"],"end":140549701,"clinical_significance":[],"id":"rs1010239585","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797041840","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549705,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140549705},{"end":140549706,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140549706,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1025183991"},{"source":"dbSNP","start":140549711,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140549711,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1797042079","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs184773256","alleles":["G","A"],"end":140549712,"feature_type":"variation","strand":1,"source":"dbSNP","start":140549712,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1195056727","alleles":["A","T"],"end":140549716,"feature_type":"variation","strand":1,"source":"dbSNP","start":140549716,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140549718,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140549718,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797042425"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140549719,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549719,"source":"dbSNP","id":"rs1016483068","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797042636","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549720,"feature_type":"variation","strand":1,"end":140549720,"alleles":["G","C"]},{"seq_region_name":"7","id":"rs1488910542","clinical_significance":[],"end":140549722,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140549722,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs981099947","end":140549723,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140549723,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1220328662","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549727,"feature_type":"variation","strand":1,"end":140549727,"alleles":["C","A"]},{"alleles":["C","T"],"end":140549730,"strand":1,"feature_type":"variation","start":140549730,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1797043088","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140549736,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549736,"clinical_significance":[],"id":"rs545951609","seq_region_name":"7"},{"id":"rs1358828997","seq_region_name":"7","clinical_significance":[],"start":140549737,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140549740,"alleles":["TGTG","TGTGTG"],"strand":1,"feature_type":"variation"},{"id":"rs971701122","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140549738,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549738,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1797043539","seq_region_name":"7","source":"dbSNP","start":140549748,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140549748,"feature_type":"variation","strand":1},{"id":"rs1242982180","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140549749,"alleles":["C","A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549749,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1334565377","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549751,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140549751},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130538265","source":"dbSNP","start":140549753,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140549753,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs923048218","clinical_significance":[],"start":140549756,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140549756,"strand":1,"feature_type":"variation"},{"start":140549759,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140549759,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs958432551","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797044540","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549767,"feature_type":"variation","strand":1,"end":140549767,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797044753","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140549768,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549768},{"source":"dbSNP","start":140549772,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140549772,"alleles":["T","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs557935993"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1304596007","source":"dbSNP","start":140549776,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["ATAGATA","ATAGATAGATA"],"end":140549782,"feature_type":"variation","strand":1},{"end":140549777,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140549777,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs909044263","clinical_significance":[]},{"start":140549779,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140549779,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1316652279","clinical_significance":[]},{"source":"dbSNP","start":140549781,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140549781,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1585604992","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1364441406","feature_type":"variation","strand":1,"alleles":["TATTTATTT","TATTT"],"end":140549789,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549781},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140549783,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549783,"clinical_significance":[],"seq_region_name":"7","id":"rs1198055412"},{"clinical_significance":[],"id":"rs552735383","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549788,"feature_type":"variation","strand":1,"end":140549788,"alleles":["T","C"]},{"source":"dbSNP","start":140549790,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140549790,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1362029127"},{"seq_region_name":"7","id":"rs186536764","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140549795,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549795,"source":"dbSNP"},{"source":"dbSNP","start":140549796,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140549796,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1797047269","seq_region_name":"7"},{"alleles":["T","C"],"end":140549799,"feature_type":"variation","strand":1,"source":"dbSNP","start":140549799,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs910404214"},{"source":"dbSNP","start":140549803,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140549803,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1208300561"},{"clinical_significance":[],"seq_region_name":"7","id":"rs947203904","end":140549807,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140549807,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140549811,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140549811,"alleles":["A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130538424","clinical_significance":[]},{"alleles":["T","C"],"end":140549813,"strand":1,"feature_type":"variation","start":140549813,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797047973","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549816,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140549816,"seq_region_name":"7","id":"rs1475610248","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797048365","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549818,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140549818},{"seq_region_name":"7","id":"rs777669187","clinical_significance":[],"strand":1,"feature_type":"variation","end":140549827,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549827,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140549829,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549829,"clinical_significance":[],"seq_region_name":"7","id":"rs1218942602"},{"seq_region_name":"7","id":"rs1043377255","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140549831,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549831,"source":"dbSNP"},{"start":140549832,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140549832,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs903093510","clinical_significance":[]},{"seq_region_name":"7","id":"rs972393970","clinical_significance":[],"start":140549833,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140549833,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140549834,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549834,"clinical_significance":[],"seq_region_name":"7","id":"rs1797049369"},{"clinical_significance":[],"id":"rs1260713739","seq_region_name":"7","source":"dbSNP","start":140549843,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140549843,"feature_type":"variation","strand":1},{"id":"rs1234349591","seq_region_name":"7","clinical_significance":[],"alleles":["C","A"],"end":140549844,"strand":1,"feature_type":"variation","start":140549844,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1421352141","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140549848,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549848,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140549849,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549849,"clinical_significance":[],"seq_region_name":"7","id":"rs923190613"},{"alleles":["G","A"],"end":140549850,"strand":1,"feature_type":"variation","start":140549850,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1402739434","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["ATCAATGGATAAATGGATAAATAATCAATCAATGGATAAATGGATAAATAA","ATCAATGGATAAATGGATAAATAA","ATCAATGGATAAATGGATAAATAATCAATCAATGGATAAATGGATAAATAATCAATCAATGGATAAATGGATAAATAA"],"end":140549904,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549854,"source":"dbSNP","seq_region_name":"7","id":"rs1176452794","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549855,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140549855,"seq_region_name":"7","id":"rs1797050579","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549857,"source":"dbSNP","strand":1,"feature_type":"variation","end":140549858,"alleles":["AA","A"],"id":"rs1403733849","seq_region_name":"7","clinical_significance":[]},{"end":140549858,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140549858,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs935370870","clinical_significance":[]},{"id":"rs1298237531","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140549864,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549864,"source":"dbSNP"},{"id":"rs1797051244","seq_region_name":"7","clinical_significance":[],"end":140549870,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140549870,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140549877,"alleles":["ATAAATAA","ATAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140549870,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585605240"},{"seq_region_name":"7","id":"rs560199553","clinical_significance":[],"strand":1,"feature_type":"variation","end":140549871,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549871,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549872,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AAA","AAAAA"],"end":140549874,"seq_region_name":"7","id":"rs1797051699","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140549879,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549879,"source":"dbSNP","seq_region_name":"7","id":"rs1333093860","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140549886,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549886,"source":"dbSNP","seq_region_name":"7","id":"rs1797052062","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs896457469","alleles":["G","C"],"end":140549888,"feature_type":"variation","strand":1,"source":"dbSNP","start":140549888,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140549895,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549895,"source":"dbSNP","seq_region_name":"7","id":"rs1797052423","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140549901,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549901,"clinical_significance":[],"id":"rs1797052599","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797052757","feature_type":"variation","strand":1,"end":140549908,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549908},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797052916","end":140549911,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140549911,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1013692971","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549913,"source":"dbSNP","strand":1,"feature_type":"variation","end":140549913,"alleles":["A","G"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549916,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140549916,"clinical_significance":[],"id":"rs1023684384","seq_region_name":"7"},{"start":140549919,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140549919,"alleles":["A","C"],"strand":1,"feature_type":"variation","id":"rs1797053358","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs889242585","alleles":["A","C","G"],"end":140549921,"feature_type":"variation","strand":1,"source":"dbSNP","start":140549921,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140549923,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549923,"clinical_significance":[],"seq_region_name":"7","id":"rs1480216572"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1264255423","end":140549932,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140549932,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs572556066","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140549934,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549934,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140549948,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549948,"source":"dbSNP","seq_region_name":"7","id":"rs1797053933","clinical_significance":[]},{"start":140549953,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140549953,"alleles":["G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs905366865","clinical_significance":[]},{"clinical_significance":[],"id":"rs1797054133","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549953,"feature_type":"variation","strand":1,"end":140549956,"alleles":["GAAG","GAAGAAG"]},{"seq_region_name":"7","id":"rs1006381736","clinical_significance":[],"start":140549955,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140549955,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140549961,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140549961,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1797054359","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1797054468","clinical_significance":[],"alleles":["T","A"],"end":140549963,"strand":1,"feature_type":"variation","start":140549963,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1195919797","clinical_significance":[],"start":140549964,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140549964,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797054697","end":140549965,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140549965,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140549966,"alleles":["A","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140549966,"source":"dbSNP","seq_region_name":"7","id":"rs1345483791","clinical_significance":[]},{"alleles":["T","C"],"end":140549967,"strand":1,"feature_type":"variation","start":140549967,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797054940","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1445365149","alleles":["G","C"],"end":140549968,"feature_type":"variation","strand":1,"source":"dbSNP","start":140549968,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs192726567","clinical_significance":[],"start":140549972,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140549972,"alleles":["C","A","T"],"strand":1,"feature_type":"variation"},{"alleles":["G","A"],"end":140549973,"feature_type":"variation","strand":1,"source":"dbSNP","start":140549973,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1484412811"},{"clinical_significance":[],"id":"rs1797055365","seq_region_name":"7","alleles":["G","A"],"end":140549978,"feature_type":"variation","strand":1,"source":"dbSNP","start":140549978,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585605425","source":"dbSNP","start":140549984,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140549984,"feature_type":"variation","strand":1},{"id":"rs962302059","seq_region_name":"7","clinical_significance":[],"start":140549989,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140549989,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1280536271","seq_region_name":"7","alleles":["T","C"],"end":140549994,"feature_type":"variation","strand":1,"source":"dbSNP","start":140549994,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1053834895","source":"dbSNP","start":140549994,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140549999,"alleles":["TATTAT","TAT"],"feature_type":"variation","strand":1},{"alleles":["A","G"],"end":140549995,"feature_type":"variation","strand":1,"source":"dbSNP","start":140549995,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1322392649"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140549999,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140549999,"clinical_significance":[],"id":"rs1797056021","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550001,"feature_type":"variation","strand":1,"end":140550001,"alleles":["C","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1797056113"},{"source":"dbSNP","start":140550006,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140550006,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1278504730"},{"seq_region_name":"7","id":"rs1797056309","clinical_significance":[],"end":140550007,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140550007,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1797056416","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140550010,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550010},{"alleles":["C","A","G","T"],"end":140550011,"strand":1,"feature_type":"variation","start":140550011,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs971733831","seq_region_name":"7","clinical_significance":[]},{"id":"rs1218591492","seq_region_name":"7","clinical_significance":[],"start":140550012,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140550012,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1324207824","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550017,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140550017},{"source":"dbSNP","start":140550023,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140550023,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797056895"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797057006","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550030,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140550030},{"seq_region_name":"7","id":"rs1797057115","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550032,"source":"dbSNP","strand":1,"feature_type":"variation","end":140550032,"alleles":["A","G"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550036,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140550036,"seq_region_name":"7","id":"rs1029968628","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550039,"feature_type":"variation","strand":1,"end":140550039,"alleles":["G","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1797057298"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1009712235","end":140550042,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140550042,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs376216655","alleles":["G","A","T"],"end":140550043,"feature_type":"variation","strand":1,"source":"dbSNP","start":140550043,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1334442796","seq_region_name":"7","feature_type":"variation","strand":1,"end":140550053,"alleles":["T","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550053},{"start":140550055,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140550061,"alleles":["TAACATT","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797057755","clinical_significance":[]},{"id":"rs1469155498","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550056,"source":"dbSNP","strand":1,"feature_type":"variation","end":140550056,"alleles":["A","G"]},{"alleles":["C","T"],"end":140550062,"strand":1,"feature_type":"variation","start":140550062,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs77013992","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550063,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140550063,"seq_region_name":"7","id":"rs752179368","clinical_significance":[]},{"end":140550065,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140550065,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1447839450","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1474444563","source":"dbSNP","start":140550071,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140550071,"feature_type":"variation","strand":1},{"alleles":["T","C"],"end":140550072,"strand":1,"feature_type":"variation","start":140550072,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1797058557","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140550073,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140550073,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1372600973","seq_region_name":"7"},{"source":"dbSNP","start":140550075,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140550075,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs947243667"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550080,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140550080,"id":"rs1797059045","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797059199","clinical_significance":[],"alleles":["AAAAA","AAAA"],"end":140550086,"strand":1,"feature_type":"variation","start":140550082,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140550084,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140550084,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1218463820","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","C"],"end":140550087,"feature_type":"variation","strand":1,"source":"dbSNP","start":140550087,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797059530"},{"id":"rs184550376","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550088,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140550088},{"clinical_significance":[],"id":"rs1585605605","seq_region_name":"7","end":140550093,"alleles":["AGAAAG","AG"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140550088,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140550090,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140550092,"alleles":["AAA","AA"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797060031"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550091,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140550091,"clinical_significance":[],"seq_region_name":"7","id":"rs1585605616"},{"id":"rs924549940","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550093,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140550093},{"id":"rs934574991","seq_region_name":"7","clinical_significance":[],"end":140550102,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140550102,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs958484901","feature_type":"variation","strand":1,"end":140550103,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550103},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550107,"feature_type":"variation","strand":1,"end":140550107,"alleles":["G","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1200063948"},{"end":140550126,"alleles":["GGGGTTAGGGGAGGGG","GGG"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140550111,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1554465310"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797061319","feature_type":"variation","strand":1,"end":140550145,"alleles":["GGGGTTAGGGGAGGGGATAGGGGTGGGGTTAGGGG","GGGGTTAGGGGAGGGGATAGGGGTGGGGTTAGGGGAGGGGATAGGGGTGGGGTTAGGGG"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550111},{"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140550112,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550112,"source":"dbSNP","id":"rs1057047172","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","A"],"end":140550113,"strand":1,"feature_type":"variation","start":140550113,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1197210082","clinical_significance":[]},{"id":"rs917925136","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140550116,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550116,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1797062116","clinical_significance":[],"alleles":["A","G"],"end":140550117,"strand":1,"feature_type":"variation","start":140550117,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140550121,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140550121,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797062327"},{"end":140550122,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140550122,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1480739797","seq_region_name":"7"},{"start":140550123,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140550123,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1269050022","clinical_significance":[]},{"clinical_significance":[],"id":"rs1797062651","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["GGGG","GGGGG"],"end":140550126,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550123},{"clinical_significance":[],"id":"rs1476749531","seq_region_name":"7","end":140550138,"alleles":["GGGGATAGGGGTGGGG","GGGG"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140550123,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140550125,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140550125,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1005935774"},{"source":"dbSNP","start":140550127,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C","T"],"end":140550127,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs190020570"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550127,"feature_type":"variation","strand":1,"end":140550127,"alleles":["A","-"],"clinical_significance":[],"seq_region_name":"7","id":"rs1797063222"},{"strand":1,"feature_type":"variation","end":140550129,"alleles":["ATA","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550127,"source":"dbSNP","id":"rs1797063366","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550128,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","G"],"end":140550128,"seq_region_name":"7","id":"rs1797063525","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550128,"feature_type":"variation","strand":1,"alleles":["TAGGGGTGGGGTTAGGGGTGGGGTTAGGGG","TAGGGGTGGGGTTAGGGG"],"end":140550157,"clinical_significance":[],"seq_region_name":"7","id":"rs199505042"},{"source":"dbSNP","start":140550129,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G","T"],"end":140550129,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs945177969"},{"seq_region_name":"7","id":"rs1400803971","clinical_significance":[],"end":140550129,"alleles":["A","-"],"strand":1,"feature_type":"variation","start":140550129,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1563133290","clinical_significance":[],"strand":1,"feature_type":"variation","end":140550133,"alleles":["AGGGG","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550129,"source":"dbSNP"},{"id":"rs1331078434","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550129,"source":"dbSNP","strand":1,"feature_type":"variation","end":140550141,"alleles":["AGGGGTGGGGTTA","-"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550130,"source":"dbSNP","strand":1,"feature_type":"variation","end":140550130,"alleles":["G","A"],"seq_region_name":"7","id":"rs1300384618","clinical_significance":[]},{"seq_region_name":"7","id":"rs1396091774","clinical_significance":[],"alleles":["G","C"],"end":140550131,"strand":1,"feature_type":"variation","start":140550131,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1797064637","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550131,"source":"dbSNP","strand":1,"feature_type":"variation","end":140550140,"alleles":["GGGTGGGGTT","-"]},{"start":140550131,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["GGGTGGGGTTAGGG","GGG"],"end":140550144,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797064740","clinical_significance":[]},{"alleles":["G","A"],"end":140550132,"feature_type":"variation","strand":1,"source":"dbSNP","start":140550132,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797064843"},{"strand":1,"feature_type":"variation","alleles":["T","-"],"end":140550134,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550134,"source":"dbSNP","seq_region_name":"7","id":"rs747313648","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550134,"feature_type":"variation","strand":1,"alleles":["T","A","C","G"],"end":140550134,"clinical_significance":[],"seq_region_name":"7","id":"rs1046310063"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550134,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TGGGGTT","-"],"end":140550140,"seq_region_name":"7","id":"rs1797065212","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797065296","source":"dbSNP","start":140550135,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140550135,"alleles":["G","C"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550135,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GGGG","GGG"],"end":140550138,"seq_region_name":"7","id":"rs1797065409","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1399864590","feature_type":"variation","strand":1,"end":140550146,"alleles":["GGGGTTAGGGGT","GGGGT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550135},{"start":140550136,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140550136,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1383862048","clinical_significance":[]},{"alleles":["GGGTTAGGGGTGGG","GGG"],"end":140550149,"feature_type":"variation","strand":1,"source":"dbSNP","start":140550136,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs776960201"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550137,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140550137,"id":"rs1797065803","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1333379584","feature_type":"variation","strand":1,"end":140550138,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550138},{"clinical_significance":[],"seq_region_name":"7","id":"rs371141619","end":140550139,"alleles":["T","A","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140550139,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1797066299","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550139,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TTA","-"],"end":140550141},{"id":"rs1234943822","seq_region_name":"7","clinical_significance":[],"start":140550141,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G","T"],"end":140550141,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140550142,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550142,"source":"dbSNP","seq_region_name":"7","id":"rs1271922690","clinical_significance":[]},{"clinical_significance":[],"id":"rs1435716675","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["GGGGTGGGGTT","-"],"end":140550152,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550142},{"clinical_significance":[],"id":"rs1797066740","seq_region_name":"7","source":"dbSNP","start":140550143,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140550143,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1209855183","seq_region_name":"7","source":"dbSNP","start":140550144,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140550144,"alleles":["G","A"],"feature_type":"variation","strand":1},{"alleles":["T","A","G"],"end":140550146,"strand":1,"feature_type":"variation","start":140550146,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs77898086","clinical_significance":[]},{"id":"rs1797067157","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140550147,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550147,"source":"dbSNP"},{"start":140550147,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140550162,"alleles":["GGGGTTAGGGGAGGGG","GGGG"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1563133344","clinical_significance":[]},{"start":140550148,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140550148,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797067391","clinical_significance":[]},{"end":140550149,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140550149,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1015928940","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1377614715","source":"dbSNP","start":140550150,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140550150,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550153,"feature_type":"variation","strand":1,"end":140550153,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1281040797"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550153,"feature_type":"variation","strand":1,"end":140550153,"alleles":["A","AA"],"clinical_significance":[],"seq_region_name":"7","id":"rs1797067843"},{"alleles":["G","A"],"end":140550154,"strand":1,"feature_type":"variation","start":140550154,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1439835933","clinical_significance":[]},{"seq_region_name":"7","id":"rs1335380964","clinical_significance":[],"end":140550158,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140550158,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1242600212","end":140550159,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140550159,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs962205086","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550159,"source":"dbSNP","strand":1,"feature_type":"variation","end":140550163,"alleles":["GGGGG","GGGG"]},{"id":"rs949330064","seq_region_name":"7","clinical_significance":[],"end":140550160,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140550160,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs542408887","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550161,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140550161},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797068737","feature_type":"variation","strand":1,"alleles":["T","A"],"end":140550166,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550166},{"clinical_significance":[],"seq_region_name":"7","id":"rs561131486","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550176,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140550176},{"start":140550179,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TTT","TTTT"],"end":140550181,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797068932","clinical_significance":[]},{"clinical_significance":[],"id":"rs1045205881","seq_region_name":"7","end":140550187,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140550187,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140550190,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140550190,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs905274359","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1006824538","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550193,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140550193},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140550206,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550206,"clinical_significance":[],"seq_region_name":"7","id":"rs1585606027"},{"end":140550209,"alleles":["TTTT","TTT"],"strand":1,"feature_type":"variation","start":140550206,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs369812480","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140550209,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140550209,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797069648"},{"start":140550210,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140550210,"alleles":["G","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs986162966","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550212,"feature_type":"variation","strand":1,"end":140550212,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1797069880"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797069984","source":"dbSNP","start":140550215,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140550215,"alleles":["A","AA"],"feature_type":"variation","strand":1},{"start":140550215,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140550215,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130539708","clinical_significance":[]},{"start":140550215,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AGAG","AG"],"end":140550218,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs910562548","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1223028354","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550222,"feature_type":"variation","strand":1,"end":140550222,"alleles":["C","T"]},{"source":"dbSNP","start":140550223,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140550223,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797070380"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140550224,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550224,"source":"dbSNP","id":"rs1563133389","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs528617469","seq_region_name":"7","feature_type":"variation","strand":1,"end":140550226,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550226},{"end":140550230,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140550230,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1490682981","seq_region_name":"7"},{"id":"rs1797070860","seq_region_name":"7","clinical_significance":[],"start":140550232,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140550232,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140550233,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550233,"clinical_significance":[],"id":"rs540705249","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs993730799","alleles":["C","T"],"end":140550234,"feature_type":"variation","strand":1,"source":"dbSNP","start":140550234,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1221143740","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140550236,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550236,"source":"dbSNP"},{"start":140550237,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140550237,"alleles":["G","T"],"strand":1,"feature_type":"variation","id":"rs1797071275","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1797071394","seq_region_name":"7","alleles":["C","T"],"end":140550239,"feature_type":"variation","strand":1,"source":"dbSNP","start":140550239,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1797071491","clinical_significance":[],"alleles":["G","A"],"end":140550241,"strand":1,"feature_type":"variation","start":140550241,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1197501353","clinical_significance":[],"start":140550244,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140550251,"alleles":["GTGCAATG","GTGCAATGTGCAATG"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140550249,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550249,"clinical_significance":[],"seq_region_name":"7","id":"rs1317441909"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797071857","source":"dbSNP","start":140550251,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140550251,"alleles":["G","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1797071988","clinical_significance":[],"strand":1,"feature_type":"variation","end":140550254,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550254,"source":"dbSNP"},{"end":140550255,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140550255,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1232974973","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550261,"source":"dbSNP","strand":1,"feature_type":"variation","end":140550261,"alleles":["T","C","G"],"seq_region_name":"7","id":"rs1797072389","clinical_significance":[]},{"id":"rs913956403","seq_region_name":"7","clinical_significance":[],"start":140550262,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140550262,"strand":1,"feature_type":"variation"},{"start":140550263,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140550263,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797072752","clinical_significance":[]},{"clinical_significance":[],"id":"rs780203251","seq_region_name":"7","source":"dbSNP","start":140550265,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140550265,"alleles":["T","C"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550268,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140550268,"clinical_significance":[],"seq_region_name":"7","id":"rs945562996"},{"clinical_significance":[],"id":"rs565306098","seq_region_name":"7","feature_type":"variation","strand":1,"end":140550269,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550269},{"source":"dbSNP","start":140550274,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140550274,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs549119686"},{"start":140550275,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140550275,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1007174049","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550276,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140550276,"clinical_significance":[],"id":"rs906820544","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1017813066","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550280,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140550280},{"strand":1,"feature_type":"variation","end":140550281,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550281,"source":"dbSNP","id":"rs1797074202","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550289,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140550289,"seq_region_name":"7","id":"rs1797074420","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs148848125","end":140550291,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140550291,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140550295,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550295,"source":"dbSNP","seq_region_name":"7","id":"rs185415685","clinical_significance":[]},{"end":140550296,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140550296,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1400452984","clinical_significance":[]},{"start":140550297,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140550297,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1164238937","clinical_significance":[]},{"seq_region_name":"7","id":"rs1393463181","clinical_significance":[],"start":140550300,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140550300,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1179093554","alleles":["C","T"],"end":140550302,"feature_type":"variation","strand":1,"source":"dbSNP","start":140550302,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1797075955","clinical_significance":[],"strand":1,"feature_type":"variation","end":140550306,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550306,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs924484530","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550309,"feature_type":"variation","strand":1,"end":140550309,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1732349884","clinical_significance":[],"end":140550311,"alleles":["AG","-"],"strand":1,"feature_type":"variation","start":140550310,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1797076307","clinical_significance":[],"start":140550312,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140550312,"strand":1,"feature_type":"variation"},{"alleles":["C","T"],"end":140550317,"feature_type":"variation","strand":1,"source":"dbSNP","start":140550317,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs955817710","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1198049951","clinical_significance":[],"start":140550318,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C"],"end":140550318,"strand":1,"feature_type":"variation"},{"start":140550319,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140550319,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797076902","clinical_significance":[]},{"id":"rs1797077063","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550324,"source":"dbSNP","strand":1,"feature_type":"variation","end":140550324,"alleles":["C","T"]},{"end":140550327,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140550327,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1797077175","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550328,"source":"dbSNP","strand":1,"feature_type":"variation","end":140550328,"alleles":["G","C"],"id":"rs1738066423","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs111987119","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140550330,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550330},{"strand":1,"feature_type":"variation","end":140550333,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550333,"source":"dbSNP","seq_region_name":"7","id":"rs1015981245","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550334,"feature_type":"variation","strand":1,"end":140550334,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1797077571"},{"clinical_significance":[],"id":"rs961802714","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550335,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140550335},{"id":"rs530325847","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140550337,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550337,"source":"dbSNP"},{"source":"dbSNP","start":140550338,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140550338,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1307335009"},{"start":140550342,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140550342,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs993777599","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550343,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140550343,"clinical_significance":[],"seq_region_name":"7","id":"rs1245212890"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550344,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140550344,"clinical_significance":[],"id":"rs949403539","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550354,"feature_type":"variation","strand":1,"end":140550358,"alleles":["ACTTA","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1219258172"},{"start":140550355,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140550355,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs548539541","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1364211109","source":"dbSNP","start":140550359,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140550359,"alleles":["A","T"],"feature_type":"variation","strand":1},{"end":140550360,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140550360,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1045054061"},{"seq_region_name":"7","id":"rs575154776","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550360,"source":"dbSNP","strand":1,"feature_type":"variation","end":140550366,"alleles":["TTTTTTT","TTTTTT","TTTTTTTT"]},{"seq_region_name":"7","id":"rs1287583734","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140550362,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550362,"source":"dbSNP"},{"start":140550364,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140550364,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1430617399","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["TTTTTTT","TTTTTTTT"],"end":140550374,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550368,"source":"dbSNP","seq_region_name":"7","id":"rs1797079448","clinical_significance":[]},{"alleles":["C","G"],"end":140550379,"feature_type":"variation","strand":1,"source":"dbSNP","start":140550379,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797079657"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550381,"source":"dbSNP","strand":1,"feature_type":"variation","end":140550381,"alleles":["G","T"],"id":"rs1797079825","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140550387,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140550387,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1354110399","seq_region_name":"7"},{"source":"dbSNP","start":140550388,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140550388,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797080187"},{"start":140550389,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140550389,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs189387030","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550390,"feature_type":"variation","strand":1,"alleles":["T","-"],"end":140550390,"clinical_significance":[],"seq_region_name":"7","id":"rs1797080607"},{"seq_region_name":"7","id":"rs1797080795","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140550391,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550391,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550393,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140550393,"clinical_significance":[],"id":"rs1797080964","seq_region_name":"7"},{"clinical_significance":[],"id":"rs2130540291","seq_region_name":"7","feature_type":"variation","strand":1,"end":140550394,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550394},{"end":140550395,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140550395,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs926728635","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130540308","source":"dbSNP","start":140550396,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140550396,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550398,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140550398,"seq_region_name":"7","id":"rs1797081318","clinical_significance":[]},{"start":140550399,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140550399,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs534446582","clinical_significance":[]},{"start":140550400,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140550400,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs954665746","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1403368255","alleles":["CAGGCTGGAGTGCAG","CAG"],"end":140550414,"feature_type":"variation","strand":1,"source":"dbSNP","start":140550400,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1797082153","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140550402,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550402},{"end":140550403,"alleles":["GG","G"],"strand":1,"feature_type":"variation","start":140550402,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1428549700","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550407,"source":"dbSNP","strand":1,"feature_type":"variation","end":140550407,"alleles":["G","C"],"seq_region_name":"7","id":"rs1273017374","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797082791","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550411,"feature_type":"variation","strand":1,"end":140550411,"alleles":["G","T"]},{"feature_type":"variation","strand":1,"end":140550415,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550415,"clinical_significance":[],"seq_region_name":"7","id":"rs2130540372"},{"end":140550417,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140550417,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797083027"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140550419,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550419,"source":"dbSNP","seq_region_name":"7","id":"rs1421048569","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs181836346","source":"dbSNP","start":140550420,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140550420,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1475042522","clinical_significance":[],"strand":1,"feature_type":"variation","end":140550421,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550421,"source":"dbSNP"},{"seq_region_name":"7","id":"rs986046738","clinical_significance":[],"start":140550422,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140550422,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1176292211","feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140550423,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550423},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550426,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140550426,"seq_region_name":"7","id":"rs1585606640","clinical_significance":[]},{"start":140550427,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140550427,"strand":1,"feature_type":"variation","id":"rs747714631","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140550433,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550433,"source":"dbSNP","id":"rs1797084337","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1237155850","source":"dbSNP","start":140550434,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140550434,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1797084605","clinical_significance":[],"start":140550435,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140550435,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1797084757","clinical_significance":[],"alleles":["C","T"],"end":140550442,"strand":1,"feature_type":"variation","start":140550442,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140550448,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140550448,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1262704256"},{"clinical_significance":[],"seq_region_name":"7","id":"rs958034843","source":"dbSNP","start":140550449,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140550449,"alleles":["C","G"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550450,"feature_type":"variation","strand":1,"end":140550450,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1797085168"},{"clinical_significance":[],"seq_region_name":"7","id":"rs560785938","end":140550453,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140550453,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1309537908","end":140550456,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140550456,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140550460,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140550460,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1654068457","clinical_significance":[]},{"clinical_significance":[],"id":"rs1052002483","seq_region_name":"7","alleles":["G","A","C","T"],"end":140550461,"feature_type":"variation","strand":1,"source":"dbSNP","start":140550461,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140550463,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140550463,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs570924731"},{"seq_region_name":"7","id":"rs375541494","clinical_significance":[],"start":140550465,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140550465,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585606741","source":"dbSNP","start":140550466,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140550466,"alleles":["T","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1370573944","clinical_significance":[],"alleles":["C","G"],"end":140550467,"strand":1,"feature_type":"variation","start":140550467,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797086349","feature_type":"variation","strand":1,"end":140550469,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550469},{"seq_region_name":"7","id":"rs1797086472","clinical_significance":[],"start":140550480,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140550480,"strand":1,"feature_type":"variation"},{"alleles":["T","C"],"end":140550492,"feature_type":"variation","strand":1,"source":"dbSNP","start":140550492,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1317792824"},{"strand":1,"feature_type":"variation","end":140550493,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550493,"source":"dbSNP","seq_region_name":"7","id":"rs1017281719","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1047035984","source":"dbSNP","start":140550494,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140550494,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797087005","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550496,"feature_type":"variation","strand":1,"end":140550496,"alleles":["T","C"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550496,"feature_type":"variation","strand":1,"end":140550500,"alleles":["TTTTT","TTTTTT"],"clinical_significance":[],"seq_region_name":"7","id":"rs1797087136"},{"end":140550501,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140550501,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797087344","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550508,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140550508,"clinical_significance":[],"seq_region_name":"7","id":"rs1797087556"},{"seq_region_name":"7","id":"rs968764200","clinical_significance":[],"alleles":["T","C"],"end":140550509,"strand":1,"feature_type":"variation","start":140550509,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1585606817","clinical_significance":[],"start":140550511,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C","T"],"end":140550511,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs928163556","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550515,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140550515},{"source":"dbSNP","start":140550518,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140550518,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797088271"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797088447","end":140550521,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140550521,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs999950171","seq_region_name":"7","clinical_significance":[],"start":140550522,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140550522,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"alleles":["T","A"],"end":140550524,"strand":1,"feature_type":"variation","start":140550524,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1055323805","clinical_significance":[]},{"start":140550526,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140550526,"alleles":["T","C","G"],"strand":1,"feature_type":"variation","id":"rs888669955","seq_region_name":"7","clinical_significance":[]},{"start":140550535,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140550535,"alleles":["G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797089010","clinical_significance":[]},{"clinical_significance":[],"id":"rs1797089137","seq_region_name":"7","end":140550538,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140550538,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550541,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140550541,"id":"rs375407348","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1031801697","feature_type":"variation","strand":1,"end":140550551,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550551},{"source":"dbSNP","start":140550554,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140550554,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1005872479"},{"alleles":["G","T"],"end":140550556,"feature_type":"variation","strand":1,"source":"dbSNP","start":140550556,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797089654"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1385719494","feature_type":"variation","strand":1,"end":140550557,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550557},{"clinical_significance":[],"id":"rs1797089963","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["TCTGCCCCTCT","TCT"],"end":140550571,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550561},{"source":"dbSNP","start":140550562,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140550562,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797090180"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550564,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GCC","GCCGCC"],"end":140550566,"seq_region_name":"7","id":"rs1185381285","clinical_significance":[]},{"end":140550569,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140550569,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1242280789"},{"seq_region_name":"7","id":"rs1442495911","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550569,"source":"dbSNP","strand":1,"feature_type":"variation","end":140550569,"alleles":["T","-"]},{"seq_region_name":"7","id":"rs1037326921","clinical_significance":[],"start":140550571,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140550571,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1481738138","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550573,"feature_type":"variation","strand":1,"end":140550573,"alleles":["A","C","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs955892175","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140550582,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550582},{"clinical_significance":[],"seq_region_name":"7","id":"rs897603084","feature_type":"variation","strand":1,"end":140550588,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550588},{"id":"rs1797091718","seq_region_name":"7","clinical_significance":[],"start":140550589,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140550589,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797091857","alleles":["G","A"],"end":140550591,"feature_type":"variation","strand":1,"source":"dbSNP","start":140550591,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797092019","source":"dbSNP","start":140550596,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140550596,"alleles":["C","T"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550599,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140550599,"seq_region_name":"7","id":"rs1797092170","clinical_significance":[]},{"clinical_significance":[],"id":"rs556849896","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550600,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140550600},{"clinical_significance":[],"seq_region_name":"7","id":"rs1360258859","source":"dbSNP","start":140550602,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140550602,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550603,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140550603,"clinical_significance":[],"id":"rs1294531058","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140550605,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550605,"source":"dbSNP","id":"rs1797092776","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550607,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140550607,"clinical_significance":[],"seq_region_name":"7","id":"rs138098322"},{"feature_type":"variation","strand":1,"alleles":["CC","C"],"end":140550616,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550615,"clinical_significance":[],"seq_region_name":"7","id":"rs1382759205"},{"seq_region_name":"7","id":"rs1308157784","clinical_significance":[],"strand":1,"feature_type":"variation","end":140550617,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550617,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563133648","feature_type":"variation","strand":1,"end":140550618,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550618},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550629,"feature_type":"variation","strand":1,"alleles":["TTTT","TTTTT"],"end":140550632,"clinical_significance":[],"seq_region_name":"7","id":"rs1393561052"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797093634","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550630,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140550630},{"clinical_significance":[],"id":"rs536546922","seq_region_name":"7","feature_type":"variation","strand":1,"end":140550633,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550633},{"end":140550634,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140550634,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs980398111"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550637,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140550637,"id":"rs2130540949","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1376390601","clinical_significance":[],"alleles":["T","G"],"end":140550639,"strand":1,"feature_type":"variation","start":140550639,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["T","G"],"end":140550644,"strand":1,"feature_type":"variation","start":140550644,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585607099","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797094318","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550649,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140550649},{"end":140550651,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140550651,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs554498198","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140550652,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550652,"clinical_significance":[],"id":"rs572980450","seq_region_name":"7"},{"start":140550653,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140550653,"strand":1,"feature_type":"variation","id":"rs1797094772","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797094924","clinical_significance":[],"strand":1,"feature_type":"variation","end":140550654,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550654,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140550662,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550662,"source":"dbSNP","id":"rs1164989997","seq_region_name":"7","clinical_significance":[]},{"end":140550663,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140550663,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1007369854"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550671,"feature_type":"variation","strand":1,"end":140550671,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1338493188"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797095371","end":140550698,"alleles":["AGGCTGGTCTTGAACTAATGACCTTAGG","AGG"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140550671,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797095552","feature_type":"variation","strand":1,"end":140550673,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550673},{"clinical_significance":[],"seq_region_name":"7","id":"rs1554465453","alleles":["T","C"],"end":140550681,"feature_type":"variation","strand":1,"source":"dbSNP","start":140550681,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs772643578","alleles":["A","T"],"end":140550683,"feature_type":"variation","strand":1,"source":"dbSNP","start":140550683,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1278739067","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550685,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140550685},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550688,"source":"dbSNP","strand":1,"feature_type":"variation","end":140550688,"alleles":["A","G"],"seq_region_name":"7","id":"rs1797096388","clinical_significance":[]},{"alleles":["T","C"],"end":140550695,"strand":1,"feature_type":"variation","start":140550695,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1159545984","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs919336563","alleles":["G","T"],"end":140550697,"feature_type":"variation","strand":1,"source":"dbSNP","start":140550697,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797096876","source":"dbSNP","start":140550698,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140550698,"alleles":["G","T"],"feature_type":"variation","strand":1},{"start":140550699,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140550699,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs1797097040","seq_region_name":"7","clinical_significance":[]},{"id":"rs762518188","seq_region_name":"7","clinical_significance":[],"start":140550702,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140550702,"alleles":["T","G"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550703,"feature_type":"variation","strand":1,"end":140550703,"alleles":["C","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1797097490"},{"seq_region_name":"7","id":"rs1490519107","clinical_significance":[],"alleles":["A","T"],"end":140550705,"strand":1,"feature_type":"variation","start":140550705,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550706,"feature_type":"variation","strand":1,"end":140550706,"alleles":["C","CCC"],"clinical_significance":[],"seq_region_name":"7","id":"rs1176866453"},{"start":140550706,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140550706,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797097815","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585607228","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550707,"source":"dbSNP","strand":1,"feature_type":"variation","end":140550707,"alleles":["A","C"]},{"end":140550708,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140550708,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1271111407","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","T"],"end":140550711,"feature_type":"variation","strand":1,"source":"dbSNP","start":140550711,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1196164914"},{"strand":1,"feature_type":"variation","end":140550712,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550712,"source":"dbSNP","id":"rs1051863934","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550727,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140550727,"id":"rs890738348","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797099087","clinical_significance":[],"strand":1,"feature_type":"variation","end":140550729,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550729,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140550735,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550735,"source":"dbSNP","seq_region_name":"7","id":"rs989523116","clinical_significance":[]},{"id":"rs943650932","seq_region_name":"7","clinical_significance":[],"start":140550739,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","G","T"],"end":140550739,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs371480968","source":"dbSNP","start":140550740,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140550740,"feature_type":"variation","strand":1},{"alleles":["A","C","G"],"end":140550747,"feature_type":"variation","strand":1,"source":"dbSNP","start":140550747,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585607304"},{"seq_region_name":"7","id":"rs1797099969","clinical_significance":[],"end":140550748,"alleles":["-","TTCATCCAGCTTTAGCTAATTTTCGTAATTTTAGTAGAGATCGGGTTTCA"],"strand":1,"feature_type":"variation","start":140550749,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1315543019","clinical_significance":[],"alleles":["C","T"],"end":140550749,"strand":1,"feature_type":"variation","start":140550749,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550750,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140550750,"clinical_significance":[],"id":"rs1253720830","seq_region_name":"7"},{"source":"dbSNP","start":140550751,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140550751,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs766858970"},{"id":"rs1797100734","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550752,"source":"dbSNP","strand":1,"feature_type":"variation","end":140550752,"alleles":["G","A"]},{"alleles":["C","G"],"end":140550753,"strand":1,"feature_type":"variation","start":140550753,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1563133758","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs540387188","source":"dbSNP","start":140550758,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140550758,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1389853478","end":140550762,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140550762,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140550763,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550763,"clinical_significance":[],"seq_region_name":"7","id":"rs780805638"},{"end":140550770,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140550770,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs891531780","clinical_significance":[]},{"seq_region_name":"7","id":"rs1455113422","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140550775,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550775,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1797102060","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["TTT","TT"],"end":140550777,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550775,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140550778,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550778,"clinical_significance":[],"seq_region_name":"7","id":"rs1797102224"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140550781,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550781,"clinical_significance":[],"seq_region_name":"7","id":"rs1187346988"},{"alleles":["GGGGG","GGGG"],"end":140550787,"strand":1,"feature_type":"variation","start":140550783,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797102555","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550785,"feature_type":"variation","strand":1,"end":140550785,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1797102731"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550786,"feature_type":"variation","strand":1,"end":140550786,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1797102847"},{"clinical_significance":[],"seq_region_name":"7","id":"rs867072298","source":"dbSNP","start":140550787,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C","T"],"end":140550787,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550792,"source":"dbSNP","strand":1,"feature_type":"variation","end":140550792,"alleles":["G","A"],"seq_region_name":"7","id":"rs1480866958","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550794,"feature_type":"variation","strand":1,"end":140550794,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1431797374"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797103342","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550798,"feature_type":"variation","strand":1,"end":140550798,"alleles":["G","C"]},{"seq_region_name":"7","id":"rs1797103458","clinical_significance":[],"alleles":["T","A"],"end":140550812,"strand":1,"feature_type":"variation","start":140550812,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140550816,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550816,"clinical_significance":[],"seq_region_name":"7","id":"rs1797103590"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797103689","feature_type":"variation","strand":1,"alleles":["T","A"],"end":140550824,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550824},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550828,"feature_type":"variation","strand":1,"end":140550828,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs186488912"},{"source":"dbSNP","start":140550829,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140550829,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797103936"},{"start":140550830,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C","G"],"end":140550830,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797104032","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550832,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140550832,"id":"rs1490209465","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1797104313","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550833,"feature_type":"variation","strand":1,"end":140550835,"alleles":["AAT","-"]},{"clinical_significance":[],"id":"rs1797104430","seq_region_name":"7","source":"dbSNP","start":140550835,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140550835,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140550838,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550838,"source":"dbSNP","seq_region_name":"7","id":"rs2130541525","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1024157107","source":"dbSNP","start":140550842,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140550842,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs577314279","seq_region_name":"7","feature_type":"variation","strand":1,"end":140550847,"alleles":["G","A","C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550847},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550852,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140550852,"clinical_significance":[],"seq_region_name":"7","id":"rs1168567855"},{"seq_region_name":"7","id":"rs969855777","clinical_significance":[],"alleles":["G","A"],"end":140550853,"strand":1,"feature_type":"variation","start":140550853,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140550858,"alleles":["G","C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550858,"clinical_significance":[],"seq_region_name":"7","id":"rs1485207139"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797105169","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550861,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140550861},{"clinical_significance":[],"seq_region_name":"7","id":"rs980046537","source":"dbSNP","start":140550865,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140550865,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1797105416","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550870,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AA","AAA"],"end":140550871},{"start":140550879,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140550879,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797105524","clinical_significance":[]},{"id":"rs367729636","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140550882,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550882,"source":"dbSNP"},{"end":140550888,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140550888,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1304807077","clinical_significance":[]},{"end":140550894,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140550894,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1322490502","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1284819751","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140550896,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550896},{"clinical_significance":[],"id":"rs1797106060","seq_region_name":"7","feature_type":"variation","strand":1,"end":140550899,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550899},{"seq_region_name":"7","id":"rs1554465495","clinical_significance":[],"alleles":["A","-"],"end":140550903,"strand":1,"feature_type":"variation","start":140550903,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs2130541645","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140550903,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550903,"source":"dbSNP"},{"alleles":["G","T"],"end":140550916,"strand":1,"feature_type":"variation","start":140550916,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1221082538","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1400410010","feature_type":"variation","strand":1,"alleles":["GAC","-"],"end":140550918,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550916},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550918,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140550918,"seq_region_name":"7","id":"rs1797106476","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797106622","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140550924,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550924,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140550925,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550925,"clinical_significance":[],"id":"rs1330034557","seq_region_name":"7"},{"start":140550926,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140550926,"strand":1,"feature_type":"variation","id":"rs1797106826","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797106941","clinical_significance":[],"end":140550941,"alleles":["AAAAATAAAAA","AAAAA"],"strand":1,"feature_type":"variation","start":140550931,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140550933,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140550939,"alleles":["AAATAAA","AAA"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797107056","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140550935,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550935,"clinical_significance":[],"seq_region_name":"7","id":"rs2130541721"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140550937,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550937,"source":"dbSNP","seq_region_name":"7","id":"rs1296142248","clinical_significance":[]},{"alleles":["A","C"],"end":140550938,"feature_type":"variation","strand":1,"source":"dbSNP","start":140550938,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1383824679"},{"alleles":["G","T"],"end":140550942,"strand":1,"feature_type":"variation","start":140550942,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs938196262","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1319634424","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140550945,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550945},{"source":"dbSNP","start":140550948,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140550948,"alleles":["T","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797107591"},{"start":140550949,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140550949,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797107690","clinical_significance":[]},{"seq_region_name":"7","id":"rs1470137997","clinical_significance":[],"strand":1,"feature_type":"variation","end":140550953,"alleles":["GGGGG","GGGG"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550949,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs990934839","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140550950,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550950},{"end":140550958,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140550958,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797108015"},{"clinical_significance":[],"seq_region_name":"7","id":"rs910173518","end":140550963,"alleles":["AGTTAG","AG"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140550958,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140550965,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140550965,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1298612290"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797108357","alleles":["A","G"],"end":140550966,"feature_type":"variation","strand":1,"source":"dbSNP","start":140550966,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797108474","feature_type":"variation","strand":1,"alleles":["A","T"],"end":140550967,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550967},{"source":"dbSNP","start":140550972,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140550972,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1797108577","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1373694838","clinical_significance":[],"start":140550974,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","T"],"end":140550974,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs941608300","clinical_significance":[],"start":140550975,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140550975,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"id":"rs1797108941","seq_region_name":"7","clinical_significance":[],"start":140550976,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140550976,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs60750216","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550977,"feature_type":"variation","strand":1,"end":140550977,"alleles":["G","A","C"]},{"start":140550982,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140550982,"alleles":["G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1204643007","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140550984,"alleles":["C","A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550984,"source":"dbSNP","seq_region_name":"7","id":"rs973810770","clinical_significance":[]},{"seq_region_name":"7","id":"rs1216736230","clinical_significance":[],"start":140550985,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140550985,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1585607764","clinical_significance":[],"start":140550986,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140550986,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs767737204","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550987,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140550987},{"feature_type":"variation","strand":1,"end":140550990,"alleles":["A","AA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140550990,"clinical_significance":[],"seq_region_name":"7","id":"rs544010902"},{"source":"dbSNP","start":140550991,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140550991,"alleles":["G","A","C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1270237419"},{"seq_region_name":"7","id":"rs1324559057","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140550992,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140550992},{"end":140550994,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140550994,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs919368119"},{"clinical_significance":[],"id":"rs1234851175","seq_region_name":"7","alleles":["G","A","T"],"end":140550995,"feature_type":"variation","strand":1,"source":"dbSNP","start":140550995,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs929381935","end":140550996,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140550996,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551002,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140551002,"seq_region_name":"7","id":"rs1797110699","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797110869","clinical_significance":[],"end":140551003,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140551003,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1253859066","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140551004,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551004,"source":"dbSNP"},{"source":"dbSNP","start":140551005,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AAAAAAAA","AAAAAAA","AAAAAAAAA"],"end":140551012,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1051533832"},{"id":"rs1414092085","seq_region_name":"7","clinical_significance":[],"end":140551006,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140551006,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563133917","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551007,"feature_type":"variation","strand":1,"end":140551007,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs1797111797","clinical_significance":[],"end":140551008,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140551008,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551010,"feature_type":"variation","strand":1,"end":140551010,"alleles":["A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1797111902"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140551012,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551012,"source":"dbSNP","seq_region_name":"7","id":"rs1397568259","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585607871","source":"dbSNP","start":140551013,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140551013,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1482748855","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551014,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140551014},{"source":"dbSNP","start":140551015,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140551015,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs987490086"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140551019,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551019,"clinical_significance":[],"id":"rs540320043","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1390026249","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551021,"feature_type":"variation","strand":1,"end":140551021,"alleles":["C","T"]},{"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140551022,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551022,"source":"dbSNP","seq_region_name":"7","id":"rs943497534","clinical_significance":[]},{"seq_region_name":"7","id":"rs1192133970","clinical_significance":[],"strand":1,"feature_type":"variation","end":140551023,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551023,"source":"dbSNP"},{"start":140551024,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140551024,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs142133473","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1441478539","source":"dbSNP","start":140551025,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140551025,"alleles":["G","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1797113123","clinical_significance":[],"strand":1,"feature_type":"variation","end":140551028,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551028,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1797113239","clinical_significance":[],"start":140551038,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140551038,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1797113356","seq_region_name":"7","source":"dbSNP","start":140551041,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140551041,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1797113454","clinical_significance":[],"alleles":["G","A"],"end":140551043,"strand":1,"feature_type":"variation","start":140551043,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551048,"source":"dbSNP","strand":1,"feature_type":"variation","end":140551048,"alleles":["C","G"],"seq_region_name":"7","id":"rs1273340940","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797113671","clinical_significance":[],"end":140551050,"alleles":["CCC","CC"],"strand":1,"feature_type":"variation","start":140551048,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["G","A"],"end":140551052,"feature_type":"variation","strand":1,"source":"dbSNP","start":140551052,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797113840"},{"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140551055,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551055,"source":"dbSNP","seq_region_name":"7","id":"rs1797114006","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551056,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140551056,"clinical_significance":[],"seq_region_name":"7","id":"rs1797114179"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551057,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140551057,"clinical_significance":[],"id":"rs2130542202","seq_region_name":"7"},{"start":140551058,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140551058,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797114342","clinical_significance":[]},{"start":140551059,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140551059,"strand":1,"feature_type":"variation","id":"rs1196965331","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797114669","feature_type":"variation","strand":1,"end":140551060,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551060},{"start":140551063,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140551063,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs866590259","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797114976","clinical_significance":[],"start":140551065,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140551065,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs753131890","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140551066,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551066},{"id":"rs560554848","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551067,"source":"dbSNP","strand":1,"feature_type":"variation","end":140551067,"alleles":["G","A"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551069,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140551069,"clinical_significance":[],"seq_region_name":"7","id":"rs1376091420"},{"feature_type":"variation","strand":1,"end":140551073,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551073,"clinical_significance":[],"seq_region_name":"7","id":"rs1797115432"},{"seq_region_name":"7","id":"rs893764512","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551074,"source":"dbSNP","strand":1,"feature_type":"variation","end":140551074,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs2130542287","clinical_significance":[],"start":140551077,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140551077,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1797115672","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551078,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140551078},{"end":140551080,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140551080,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797115786","clinical_significance":[]},{"source":"dbSNP","start":140551081,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140551081,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1797115893","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1797115989","clinical_significance":[],"strand":1,"feature_type":"variation","end":140551082,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551082,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1797116079","clinical_significance":[],"strand":1,"feature_type":"variation","end":140551083,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551083,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1298521518","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551085,"source":"dbSNP","strand":1,"feature_type":"variation","end":140551087,"alleles":["GAG","GAGAG"]},{"source":"dbSNP","start":140551087,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140551087,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1797116308","seq_region_name":"7"},{"id":"rs1362220002","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551088,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140551088},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140551090,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551090,"clinical_significance":[],"seq_region_name":"7","id":"rs1052757519"},{"source":"dbSNP","start":140551094,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140551094,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797116646"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551098,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140551098,"clinical_significance":[],"seq_region_name":"7","id":"rs1336520301"},{"clinical_significance":[],"id":"rs189689654","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140551099,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551099},{"strand":1,"feature_type":"variation","end":140551101,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551101,"source":"dbSNP","seq_region_name":"7","id":"rs527850081","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140551103,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551103,"source":"dbSNP","seq_region_name":"7","id":"rs546308561","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551106,"feature_type":"variation","strand":1,"alleles":["G","C","T"],"end":140551106,"clinical_significance":[],"seq_region_name":"7","id":"rs1024021707"},{"strand":1,"feature_type":"variation","end":140551110,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551110,"source":"dbSNP","seq_region_name":"7","id":"rs1797117505","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140551118,"alleles":["T","C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551118,"clinical_significance":[],"seq_region_name":"7","id":"rs905704233"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797117929","feature_type":"variation","strand":1,"end":140551121,"alleles":["TGGT","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551118},{"alleles":["G","A"],"end":140551120,"strand":1,"feature_type":"variation","start":140551120,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797118119","clinical_significance":[]},{"end":140551123,"alleles":["-","GC"],"strand":1,"feature_type":"variation","start":140551124,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1797118398","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","T"],"end":140551124,"feature_type":"variation","strand":1,"source":"dbSNP","start":140551124,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797118575"},{"source":"dbSNP","start":140551125,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140551125,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1383994648"},{"clinical_significance":[],"id":"rs1021254046","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551129,"feature_type":"variation","strand":1,"end":140551129,"alleles":["C","G","T"]},{"strand":1,"feature_type":"variation","end":140551130,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551130,"source":"dbSNP","seq_region_name":"7","id":"rs1001767545","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1016893751","feature_type":"variation","strand":1,"end":140551136,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551136},{"seq_region_name":"7","id":"rs962930364","clinical_significance":[],"start":140551137,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140551137,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140551150,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140551150,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797119671"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1250391313","alleles":["T","C"],"end":140551153,"feature_type":"variation","strand":1,"source":"dbSNP","start":140551153,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1797119896","clinical_significance":[],"start":140551155,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140551155,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1222677105","source":"dbSNP","start":140551156,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140551156,"alleles":["C","T"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140551157,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551157,"source":"dbSNP","seq_region_name":"7","id":"rs1797120118","clinical_significance":[]},{"seq_region_name":"7","id":"rs1361491274","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["TGGGTG","TG"],"end":140551162,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551157,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797120223","end":140551158,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140551158,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797120339","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551160,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140551160},{"start":140551161,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140551161,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797120477","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs373415872","source":"dbSNP","start":140551162,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140551162,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1387979931","clinical_significance":[],"strand":1,"feature_type":"variation","end":140551162,"alleles":["G","GCGG"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551162,"source":"dbSNP"},{"end":140551165,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140551165,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1797120793","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1298602392","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551166,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140551166},{"seq_region_name":"7","id":"rs1227461543","clinical_significance":[],"alleles":["C","T"],"end":140551169,"strand":1,"feature_type":"variation","start":140551169,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140551170,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551170,"clinical_significance":[],"seq_region_name":"7","id":"rs145997588"},{"seq_region_name":"7","id":"rs2130542639","clinical_significance":[],"start":140551171,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140551171,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140551172,"alleles":["G","C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551172,"source":"dbSNP","seq_region_name":"7","id":"rs1237120277","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797121411","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140551173,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551173,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140551176,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551176,"clinical_significance":[],"id":"rs1797121525","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140551178,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551178,"clinical_significance":[],"id":"rs1585608244","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs180925738","feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140551193,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551193},{"clinical_significance":[],"seq_region_name":"7","id":"rs1406905172","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551194,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140551194},{"feature_type":"variation","strand":1,"end":140551198,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551198,"clinical_significance":[],"id":"rs1797122093","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140551222,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551222,"source":"dbSNP","seq_region_name":"7","id":"rs1797122270","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551228,"source":"dbSNP","strand":1,"feature_type":"variation","end":140551228,"alleles":["A","T"],"id":"rs1797122448","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551230,"source":"dbSNP","strand":1,"feature_type":"variation","end":140551230,"alleles":["G","A"],"id":"rs950678137","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","A"],"end":140551231,"feature_type":"variation","strand":1,"source":"dbSNP","start":140551231,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585608278"},{"start":140551232,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140551232,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797122970","clinical_significance":[]},{"alleles":["GG","G"],"end":140551233,"feature_type":"variation","strand":1,"source":"dbSNP","start":140551232,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797123138"},{"feature_type":"variation","strand":1,"end":140551234,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551234,"clinical_significance":[],"id":"rs1797123320","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs186346384","source":"dbSNP","start":140551237,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140551237,"alleles":["T","C","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1401601204","clinical_significance":[],"start":140551239,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140551239,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140551244,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551244,"clinical_significance":[],"id":"rs987521330","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551248,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140551248,"id":"rs1797123741","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140551251,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551251,"clinical_significance":[],"id":"rs1797123841","seq_region_name":"7"},{"id":"rs1471405744","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140551253,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551253,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551256,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140551256,"clinical_significance":[],"id":"rs191594423","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140551257,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551257,"source":"dbSNP","id":"rs536188893","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1199438747","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551258,"source":"dbSNP","strand":1,"feature_type":"variation","end":140551258,"alleles":["C","T"]},{"clinical_significance":[],"id":"rs1797124350","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551261,"feature_type":"variation","strand":1,"end":140551267,"alleles":["CTGCCCT","CTGCCCTGCCCT"]},{"id":"rs113350920","seq_region_name":"7","clinical_significance":[],"start":140551265,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140551265,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585608344","feature_type":"variation","strand":1,"end":140551267,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551267},{"clinical_significance":[],"id":"rs1242025335","seq_region_name":"7","alleles":["C","T"],"end":140551268,"feature_type":"variation","strand":1,"source":"dbSNP","start":140551268,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1489110187","source":"dbSNP","start":140551270,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140551270,"alleles":["A","C"],"feature_type":"variation","strand":1},{"id":"rs1585608375","seq_region_name":"7","clinical_significance":[],"start":140551274,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140551274,"alleles":["T","G"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551278,"feature_type":"variation","strand":1,"end":140551278,"alleles":["C","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1192941706"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551279,"feature_type":"variation","strand":1,"end":140551279,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs112877005"},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140551283,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551283,"clinical_significance":[],"seq_region_name":"7","id":"rs1585608410"},{"id":"rs1585608418","seq_region_name":"7","clinical_significance":[],"start":140551286,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","T"],"end":140551286,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797125408","source":"dbSNP","start":140551287,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140551287,"alleles":["A","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1286045864","alleles":["G","C"],"end":140551289,"feature_type":"variation","strand":1,"source":"dbSNP","start":140551289,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140551290,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140551290,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797125586","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140551292,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551292,"source":"dbSNP","seq_region_name":"7","id":"rs1585608434","clinical_significance":[]},{"source":"dbSNP","start":140551294,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140551294,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130542956"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1453939625","end":140551295,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140551295,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140551296,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140551296,"alleles":["T","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1328737152"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551296,"feature_type":"variation","strand":1,"end":140551299,"alleles":["TCTC","TC"],"clinical_significance":[],"seq_region_name":"7","id":"rs1206659230"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551297,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140551297,"id":"rs1797126146","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140551298,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A","C"],"end":140551298,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1225386947"},{"seq_region_name":"7","id":"rs1284176629","clinical_significance":[],"alleles":["T","-"],"end":140551298,"strand":1,"feature_type":"variation","start":140551298,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1797126474","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["TCA","-"],"end":140551300,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551298,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1343747241","alleles":["C","-"],"end":140551299,"feature_type":"variation","strand":1,"source":"dbSNP","start":140551299,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140551299,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551299,"source":"dbSNP","seq_region_name":"7","id":"rs1432071842","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1491301814","end":140551300,"alleles":["CA","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140551299,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797126833","feature_type":"variation","strand":1,"alleles":["CAA","-"],"end":140551301,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551299},{"clinical_significance":[],"id":"rs1797126926","seq_region_name":"7","alleles":["A","C"],"end":140551300,"feature_type":"variation","strand":1,"source":"dbSNP","start":140551300,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1797127020","seq_region_name":"7","end":140551301,"alleles":["AA","AAGAAAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140551300,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs529992901","clinical_significance":[],"end":140551322,"alleles":["AAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAA","AAAAAAAAAA","AAAAAAAAAAA","AAAAAAAAAAAA","AAAAAAAAAAAAA","AAAAAAAAAAAAAA","AAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA"],"strand":1,"feature_type":"variation","start":140551300,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1797128035","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551301,"source":"dbSNP","strand":1,"feature_type":"variation","end":140551301,"alleles":["A","C","T"]},{"alleles":["A","C","T"],"end":140551309,"strand":1,"feature_type":"variation","start":140551309,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs533942253","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130543168","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551313,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140551313},{"feature_type":"variation","strand":1,"alleles":["AAAAAAAAAAGAAA","AAA"],"end":140551326,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551313,"clinical_significance":[],"id":"rs1797128265","seq_region_name":"7"},{"id":"rs1215304963","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551314,"source":"dbSNP","strand":1,"feature_type":"variation","end":140551313,"alleles":["-","G"]},{"start":140551314,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140551314,"alleles":["A","G"],"strand":1,"feature_type":"variation","id":"rs1364633227","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs190551207","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551315,"source":"dbSNP","strand":1,"feature_type":"variation","end":140551315,"alleles":["A","G"]},{"alleles":["-","G"],"end":140551315,"strand":1,"feature_type":"variation","start":140551316,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797128630","clinical_significance":[]},{"clinical_significance":[],"id":"rs1797128726","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551316,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140551316},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551317,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140551317,"seq_region_name":"7","id":"rs1384015267","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1382456919","alleles":["AAAAAAGAAA","AAA"],"end":140551326,"feature_type":"variation","strand":1,"source":"dbSNP","start":140551317,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551318,"source":"dbSNP","strand":1,"feature_type":"variation","end":140551318,"alleles":["A","G"],"id":"rs990980652","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1339158984","end":140551326,"alleles":["AAAAAGAAA","AAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140551318,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1157866704","source":"dbSNP","start":140551319,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C","G","T"],"end":140551319,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140551320,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551320,"clinical_significance":[],"seq_region_name":"7","id":"rs1174729724"},{"seq_region_name":"7","id":"rs1797129460","clinical_significance":[],"alleles":["A","T"],"end":140551321,"strand":1,"feature_type":"variation","start":140551321,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1350360592","seq_region_name":"7","end":140551325,"alleles":["AAGAA","AA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140551321,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1410054814","seq_region_name":"7","end":140551327,"alleles":["AAGAAAG","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140551321,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140551321,"alleles":["-","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551322,"clinical_significance":[],"id":"rs1797129759","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1459403773","alleles":["AGA","A"],"end":140551324,"feature_type":"variation","strand":1,"source":"dbSNP","start":140551322,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["G","-"],"end":140551323,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551323,"source":"dbSNP","id":"rs375522862","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs888103521","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551323,"source":"dbSNP","strand":1,"feature_type":"variation","end":140551323,"alleles":["G","A","C"]},{"feature_type":"variation","strand":1,"end":140551328,"alleles":["GAAAGG","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551323,"clinical_significance":[],"seq_region_name":"7","id":"rs1797130186"},{"source":"dbSNP","start":140551324,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AAA","AA"],"end":140551326,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797130268"},{"alleles":["A","G"],"end":140551325,"feature_type":"variation","strand":1,"source":"dbSNP","start":140551325,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1797130356","seq_region_name":"7"},{"end":140551327,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140551327,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1243497952","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797130562","feature_type":"variation","strand":1,"end":140551328,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551328},{"feature_type":"variation","strand":1,"end":140551329,"alleles":["A","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551329,"clinical_significance":[],"seq_region_name":"7","id":"rs1185263919"},{"strand":1,"feature_type":"variation","end":140551333,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551333,"source":"dbSNP","id":"rs1585608757","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1237135431","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551336,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140551336},{"strand":1,"feature_type":"variation","end":140551339,"alleles":["AAAA","AAA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551336,"source":"dbSNP","id":"rs1482393808","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs964944372","alleles":["A","G"],"end":140551339,"feature_type":"variation","strand":1,"source":"dbSNP","start":140551339,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140551340,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140551340,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1005311213","clinical_significance":[]},{"source":"dbSNP","start":140551341,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140551341,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797131418"},{"clinical_significance":[],"seq_region_name":"7","id":"rs571414770","source":"dbSNP","start":140551341,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140551347,"alleles":["AAAAAAA","AAAAAA","AAAAAAAA","AAAAAAAAAAA"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140551343,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551343,"clinical_significance":[],"seq_region_name":"7","id":"rs1797131706"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551344,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140551344,"clinical_significance":[],"seq_region_name":"7","id":"rs1228279982"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140551347,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551347,"source":"dbSNP","seq_region_name":"7","id":"rs1360837463","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797132015","clinical_significance":[],"start":140551348,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140551348,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140551349,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551349,"clinical_significance":[],"seq_region_name":"7","id":"rs1797132118"},{"clinical_significance":[],"id":"rs1797132218","seq_region_name":"7","feature_type":"variation","strand":1,"end":140551350,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551350},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551352,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140551352,"clinical_significance":[],"seq_region_name":"7","id":"rs2130543513"},{"source":"dbSNP","start":140551355,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140551355,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797132313"},{"seq_region_name":"7","id":"rs975297575","clinical_significance":[],"start":140551358,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140551358,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140551363,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551363,"clinical_significance":[],"id":"rs1563134219","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797132656","end":140551364,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140551364,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs926253657","alleles":["C","T"],"end":140551370,"feature_type":"variation","strand":1,"source":"dbSNP","start":140551370,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs577454501","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551371,"feature_type":"variation","strand":1,"end":140551371,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs111329703","clinical_significance":[],"alleles":["G","C"],"end":140551373,"strand":1,"feature_type":"variation","start":140551373,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1797133090","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551375,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140551375},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140551377,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551377,"clinical_significance":[],"seq_region_name":"7","id":"rs35735479"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1053340469","alleles":["A","G"],"end":140551378,"feature_type":"variation","strand":1,"source":"dbSNP","start":140551378,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797133400","feature_type":"variation","strand":1,"end":140551379,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551379},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797133498","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140551381,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551381},{"alleles":["G","A"],"end":140551382,"strand":1,"feature_type":"variation","start":140551382,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs562897938","clinical_significance":[]},{"id":"rs764377569","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140551387,"strand":1,"feature_type":"variation","start":140551387,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140551389,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140551389,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs112821320","seq_region_name":"7"},{"seq_region_name":"7","id":"rs890247355","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551391,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","G","T"],"end":140551391},{"start":140551392,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140551392,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs949666330","clinical_significance":[]},{"id":"rs1045542549","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551393,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C","T"],"end":140551393},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551394,"feature_type":"variation","strand":1,"end":140551394,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1179387066"},{"clinical_significance":[],"id":"rs1797134668","seq_region_name":"7","feature_type":"variation","strand":1,"end":140551400,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551400},{"start":140551403,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140551403,"strand":1,"feature_type":"variation","id":"rs905607561","seq_region_name":"7","clinical_significance":[]},{"end":140551404,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140551404,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1413297053","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797135221","feature_type":"variation","strand":1,"end":140551408,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551408},{"source":"dbSNP","start":140551410,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140551410,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1001399888","seq_region_name":"7"},{"seq_region_name":"7","id":"rs753960016","clinical_significance":[],"start":140551414,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140551414,"strand":1,"feature_type":"variation"},{"start":140551417,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140551417,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1341572175","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1481768757","feature_type":"variation","strand":1,"end":140551418,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551418},{"id":"rs1438102125","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551419,"source":"dbSNP","strand":1,"feature_type":"variation","end":140551419,"alleles":["C","T"]},{"id":"rs757467638","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140551426,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551426,"source":"dbSNP"},{"alleles":["G","A"],"end":140551427,"strand":1,"feature_type":"variation","start":140551427,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1042321029","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140551429,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551429,"clinical_significance":[],"id":"rs1490651349","seq_region_name":"7"},{"id":"rs1797136170","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551432,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140551432},{"end":140551433,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140551433,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs898302527","clinical_significance":[]},{"end":140551434,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140551434,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797136399"},{"clinical_significance":[],"id":"rs1797136495","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140551440,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551440},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140551443,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551443,"clinical_significance":[],"seq_region_name":"7","id":"rs2130543792"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551444,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140551444,"clinical_significance":[],"seq_region_name":"7","id":"rs1242984217"},{"end":140551445,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140551445,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797136699"},{"alleles":["T","C"],"end":140551447,"feature_type":"variation","strand":1,"source":"dbSNP","start":140551447,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1403271617"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551449,"feature_type":"variation","strand":1,"end":140551449,"alleles":["C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1797136920"},{"id":"rs868745312","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551451,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140551451},{"source":"dbSNP","start":140551453,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140551453,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1321527946"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551463,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140551463,"clinical_significance":[],"seq_region_name":"7","id":"rs1797137204"},{"seq_region_name":"7","id":"rs994065961","clinical_significance":[],"alleles":["C","T"],"end":140551464,"strand":1,"feature_type":"variation","start":140551464,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs542172171","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551465,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140551465},{"clinical_significance":[],"seq_region_name":"7","id":"rs1352020689","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140551467,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551467},{"seq_region_name":"7","id":"rs1305628118","clinical_significance":[],"start":140551468,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140551468,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140551474,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140551517,"alleles":["ACATGTGGGCCATCTCACTGTCTAGGAGCATGGGAGACATGTGG","ACATGTGGGCCATCTCACTGTCTAGGAGCATGGGAGACATGTGGGCCATCTCACTGTCTAGGAGCATGGGAGACATGTGG"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1797137766","seq_region_name":"7"},{"id":"rs1797137871","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551477,"source":"dbSNP","strand":1,"feature_type":"variation","end":140551477,"alleles":["T","C"]},{"end":140551478,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140551478,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797137992"},{"source":"dbSNP","start":140551482,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140551482,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1797138110","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797138213","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551483,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140551483},{"clinical_significance":[],"id":"rs1465671518","seq_region_name":"7","source":"dbSNP","start":140551484,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140551484,"alleles":["C","T"],"feature_type":"variation","strand":1},{"start":140551489,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140551489,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797138430","clinical_significance":[]},{"end":140551495,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140551495,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1025479261"},{"clinical_significance":[],"id":"rs1003571749","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551501,"feature_type":"variation","strand":1,"end":140551501,"alleles":["G","C","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551503,"feature_type":"variation","strand":1,"end":140551503,"alleles":["A","G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1456156220"},{"seq_region_name":"7","id":"rs1797138939","clinical_significance":[],"start":140551505,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140551505,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551506,"source":"dbSNP","strand":1,"feature_type":"variation","end":140551506,"alleles":["G","T"],"id":"rs1797139069","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140551511,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140551511,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs865832715","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551512,"feature_type":"variation","strand":1,"end":140551512,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1008849295"},{"strand":1,"feature_type":"variation","end":140551513,"alleles":["AT","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551512,"source":"dbSNP","seq_region_name":"7","id":"rs1797139445","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1019009543","feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140551513,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551513},{"clinical_significance":[],"seq_region_name":"7","id":"rs1181477074","source":"dbSNP","start":140551515,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140551515,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1208271415","seq_region_name":"7","end":140551517,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140551517,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1480807195","feature_type":"variation","strand":1,"end":140551519,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551519},{"clinical_significance":[],"id":"rs1012288605","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551520,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140551520},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797140006","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551524,"feature_type":"variation","strand":1,"end":140551524,"alleles":["C","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1380344259","alleles":["G","A"],"end":140551527,"feature_type":"variation","strand":1,"source":"dbSNP","start":140551527,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130544073","feature_type":"variation","strand":1,"alleles":["GCGC","GC"],"end":140551530,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551527},{"clinical_significance":[],"id":"rs1230440979","seq_region_name":"7","end":140551528,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140551528,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140551529,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140551529,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs965142768","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140551530,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551530,"source":"dbSNP","seq_region_name":"7","id":"rs974826395","clinical_significance":[]},{"end":140551533,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140551533,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797140628"},{"source":"dbSNP","start":140551535,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140551535,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs962861787"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797140828","source":"dbSNP","start":140551536,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140551536,"alleles":["C","G"],"feature_type":"variation","strand":1},{"alleles":["T","C"],"end":140551538,"feature_type":"variation","strand":1,"source":"dbSNP","start":140551538,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1218452768","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs183087625","feature_type":"variation","strand":1,"end":140551540,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551540},{"clinical_significance":[],"id":"rs918867410","seq_region_name":"7","source":"dbSNP","start":140551542,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140551542,"alleles":["G","A"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551544,"feature_type":"variation","strand":1,"end":140551544,"alleles":["C","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs955809958"},{"end":140551547,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140551547,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs987189988","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2968564","alleles":["G","A","C","T"],"end":140551549,"feature_type":"variation","strand":1,"source":"dbSNP","start":140551549,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs957522952","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140551550,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551550,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1260104705","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551551,"source":"dbSNP","strand":1,"feature_type":"variation","end":140551551,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1797141738","clinical_significance":[],"alleles":["G","C"],"end":140551554,"strand":1,"feature_type":"variation","start":140551554,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140551555,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140551555,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797141850","clinical_significance":[]},{"end":140551556,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140551556,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797141952","clinical_significance":[]},{"source":"dbSNP","start":140551559,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140551559,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1037150091"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1456568229","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551561,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140551561},{"clinical_significance":[],"seq_region_name":"7","id":"rs989071509","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551569,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140551569},{"start":140551575,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140551575,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs913479126","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs898012944","seq_region_name":"7","end":140551577,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140551577,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1390007154","clinical_significance":[],"start":140551582,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140551582,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140551590,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140551590,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797142676"},{"seq_region_name":"7","id":"rs1289213718","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551594,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140551594},{"clinical_significance":[],"seq_region_name":"7","id":"rs1458626172","source":"dbSNP","start":140551599,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140551599,"alleles":["G","A"],"feature_type":"variation","strand":1},{"start":140551604,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140551604,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797142979","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140551605,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551605,"source":"dbSNP","id":"rs911570468","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140551607,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551607,"clinical_significance":[],"id":"rs1797143219","seq_region_name":"7"},{"id":"rs1585609571","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140551610,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551610,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140551611,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551611,"source":"dbSNP","seq_region_name":"7","id":"rs1797143423","clinical_significance":[]},{"start":140551627,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140551627,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs942979399","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140551628,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551628,"source":"dbSNP","id":"rs1797143632","seq_region_name":"7","clinical_significance":[]},{"id":"rs1470315480","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551632,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140551632},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797143825","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140551633,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551633},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551638,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140551638,"clinical_significance":[],"seq_region_name":"7","id":"rs2130544361"},{"strand":1,"feature_type":"variation","end":140551641,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551641,"source":"dbSNP","id":"rs1431512903","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1196935935","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140551642,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551642,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1797144119","clinical_significance":[],"alleles":["G","T"],"end":140551643,"strand":1,"feature_type":"variation","start":140551643,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140551645,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551645,"source":"dbSNP","seq_region_name":"7","id":"rs1797144230","clinical_significance":[]},{"source":"dbSNP","start":140551647,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140551647,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797144326"},{"feature_type":"variation","strand":1,"end":140551653,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551653,"clinical_significance":[],"seq_region_name":"7","id":"rs1433101038"},{"seq_region_name":"7","id":"rs1797144552","clinical_significance":[],"start":140551656,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140551656,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["C","A","G"],"end":140551658,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551658,"clinical_significance":[],"id":"rs1038822943","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140551659,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551659,"source":"dbSNP","seq_region_name":"7","id":"rs1797144789","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551660,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140551660,"clinical_significance":[],"seq_region_name":"7","id":"rs1797144897"},{"clinical_significance":[],"seq_region_name":"7","id":"rs530604199","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140551662,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551662},{"start":140551662,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TGTG","TG"],"end":140551665,"strand":1,"feature_type":"variation","id":"rs1463850480","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140551666,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551666,"clinical_significance":[],"seq_region_name":"7","id":"rs1563134500"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1207691065","end":140551668,"alleles":["TT","TTT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140551667,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1323859629","end":140551673,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140551673,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140551674,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140551674,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797145578","clinical_significance":[]},{"end":140551676,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140551676,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs949740791"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551677,"source":"dbSNP","strand":1,"feature_type":"variation","end":140551677,"alleles":["A","T"],"seq_region_name":"7","id":"rs1042597348","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs780115632","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551685,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140551685},{"end":140551689,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140551689,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1230506167","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551693,"source":"dbSNP","strand":1,"feature_type":"variation","end":140551693,"alleles":["T","C"],"seq_region_name":"7","id":"rs1045408841","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1296214021","feature_type":"variation","strand":1,"alleles":["C","-"],"end":140551700,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551700},{"end":140551701,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140551701,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1436956913"},{"alleles":["G","C"],"end":140551702,"feature_type":"variation","strand":1,"source":"dbSNP","start":140551702,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797146430"},{"seq_region_name":"7","id":"rs927095310","clinical_significance":[],"start":140551708,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140551708,"alleles":["C","A","G"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551718,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140551718,"clinical_significance":[],"seq_region_name":"7","id":"rs2948384"},{"clinical_significance":[],"id":"rs1797146770","seq_region_name":"7","source":"dbSNP","start":140551723,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TCT","T"],"end":140551725,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1797146872","clinical_significance":[],"start":140551729,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140551729,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs746981868","source":"dbSNP","start":140551730,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","G"],"end":140551730,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1797147084","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140551731,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551731,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["CTGCT","CT"],"end":140551735,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551731,"clinical_significance":[],"seq_region_name":"7","id":"rs1362795117"},{"alleles":["T","C"],"end":140551732,"feature_type":"variation","strand":1,"source":"dbSNP","start":140551732,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1319697654"},{"seq_region_name":"7","id":"rs1470423840","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551735,"source":"dbSNP","strand":1,"feature_type":"variation","end":140551743,"alleles":["TCTTCTTCT","TCTTCT"]},{"strand":1,"feature_type":"variation","end":140551736,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551736,"source":"dbSNP","id":"rs1038101862","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs898328407","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551744,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140551744},{"clinical_significance":[],"seq_region_name":"7","id":"rs1417040431","source":"dbSNP","start":140551746,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140551746,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1003877088","alleles":["T","G"],"end":140551747,"feature_type":"variation","strand":1,"source":"dbSNP","start":140551747,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140551748,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140551748,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs527880848"},{"strand":1,"feature_type":"variation","end":140551750,"alleles":["AC","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551749,"source":"dbSNP","id":"rs1171064511","seq_region_name":"7","clinical_significance":[]},{"id":"rs1420838719","seq_region_name":"7","clinical_significance":[],"start":140551750,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140551750,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551752,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140551752,"clinical_significance":[],"id":"rs1797148430","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1047004449","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140551756,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551756,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1448257555","clinical_significance":[],"start":140551761,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140551761,"strand":1,"feature_type":"variation"},{"id":"rs10230408","seq_region_name":"7","clinical_significance":[],"start":140551775,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140551775,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797148896","alleles":["TT","TTCTT"],"end":140551781,"feature_type":"variation","strand":1,"source":"dbSNP","start":140551780,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140551786,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551786,"clinical_significance":[],"seq_region_name":"7","id":"rs1797149066"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1008880459","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551788,"feature_type":"variation","strand":1,"end":140551788,"alleles":["T","C","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797149455","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551789,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140551789},{"clinical_significance":[],"id":"rs10230417","seq_region_name":"7","alleles":["T","C"],"end":140551795,"feature_type":"variation","strand":1,"source":"dbSNP","start":140551795,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs532105958","seq_region_name":"7","clinical_significance":[],"start":140551799,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140551799,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1585609925","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551800,"feature_type":"variation","strand":1,"end":140551800,"alleles":["G","A"]},{"end":140551804,"alleles":["A","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140551804,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs74878199"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1343712890","source":"dbSNP","start":140551808,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140551808,"feature_type":"variation","strand":1},{"end":140551809,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140551809,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130544812","clinical_significance":[]},{"source":"dbSNP","start":140551822,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140551822,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1033064805"},{"feature_type":"variation","strand":1,"end":140551825,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551825,"clinical_significance":[],"seq_region_name":"7","id":"rs1797150797"},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140551828,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551828,"clinical_significance":[],"seq_region_name":"7","id":"rs77539544"},{"seq_region_name":"7","id":"rs1230489961","clinical_significance":[],"strand":1,"feature_type":"variation","end":140551829,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551829,"source":"dbSNP"},{"seq_region_name":"7","id":"rs769327848","clinical_significance":[],"end":140551837,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140551837,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797151410","end":140551840,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140551840,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs529665633","clinical_significance":[],"alleles":["C","T"],"end":140551841,"strand":1,"feature_type":"variation","start":140551841,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140551842,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551842,"clinical_significance":[],"seq_region_name":"7","id":"rs141355266"},{"feature_type":"variation","strand":1,"alleles":["TCTGGTTCTGGTTCTG","TCTGGTTCTG","TCTGGTTCTGGTTCTGGTTCTG"],"end":140551857,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551842,"clinical_significance":[],"seq_region_name":"7","id":"rs538591358"},{"seq_region_name":"7","id":"rs1280102277","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551846,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140551846},{"clinical_significance":[],"seq_region_name":"7","id":"rs1316140379","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140551847,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551847},{"id":"rs1797151977","seq_region_name":"7","clinical_significance":[],"end":140551851,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140551851,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551852,"feature_type":"variation","strand":1,"end":140551852,"alleles":["G","T"],"clinical_significance":[],"id":"rs1797152096","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs748155615","source":"dbSNP","start":140551858,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140551858,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1797152302","seq_region_name":"7","end":140551859,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140551859,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1026223576","clinical_significance":[],"start":140551865,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140551865,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797152537","end":140551868,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140551868,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1797152644","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551869,"source":"dbSNP","strand":1,"feature_type":"variation","end":140551869,"alleles":["T","C"]},{"start":140551881,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140551881,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797152759","clinical_significance":[]},{"alleles":["C","T"],"end":140551883,"strand":1,"feature_type":"variation","start":140551883,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs971628463","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs771879083","seq_region_name":"7","alleles":["G","A","C","T"],"end":140551884,"feature_type":"variation","strand":1,"source":"dbSNP","start":140551884,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140551888,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140551888,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1797153163","seq_region_name":"7","clinical_significance":[]},{"id":"rs1309984058","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551891,"source":"dbSNP","strand":1,"feature_type":"variation","end":140551891,"alleles":["C","T"]},{"source":"dbSNP","start":140551896,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140551896,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs773149417"},{"clinical_significance":[],"id":"rs1797153515","seq_region_name":"7","feature_type":"variation","strand":1,"end":140551897,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551897},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551899,"feature_type":"variation","strand":1,"end":140551899,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1797153624"},{"seq_region_name":"7","id":"rs1428373952","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551903,"source":"dbSNP","strand":1,"feature_type":"variation","end":140551903,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs926972333","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551904,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140551904},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551905,"source":"dbSNP","strand":1,"feature_type":"variation","end":140551905,"alleles":["C","T"],"seq_region_name":"7","id":"rs987462792","clinical_significance":[]},{"seq_region_name":"7","id":"rs1164537956","clinical_significance":[],"start":140551906,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140551906,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1755711940","source":"dbSNP","start":140551912,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140551912,"alleles":["T","-"],"feature_type":"variation","strand":1},{"start":140551916,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G","T"],"end":140551916,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs936986212","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551919,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140551919,"clinical_significance":[],"seq_region_name":"7","id":"rs1369797768"},{"alleles":["C","A"],"end":140551922,"strand":1,"feature_type":"variation","start":140551922,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797154452","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140551924,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551924,"source":"dbSNP","id":"rs1184991127","seq_region_name":"7","clinical_significance":[]},{"start":140551929,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140551929,"strand":1,"feature_type":"variation","id":"rs974261605","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1256556527","clinical_significance":[],"start":140551930,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140551930,"strand":1,"feature_type":"variation"},{"start":140551934,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140551934,"alleles":["A","G"],"strand":1,"feature_type":"variation","id":"rs1797155191","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs187758814","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551944,"feature_type":"variation","strand":1,"end":140551944,"alleles":["A","C"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551945,"source":"dbSNP","strand":1,"feature_type":"variation","end":140551945,"alleles":["G","A"],"seq_region_name":"7","id":"rs1797155562","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551948,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140551948,"clinical_significance":[],"seq_region_name":"7","id":"rs1797155922"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551949,"feature_type":"variation","strand":1,"end":140551949,"alleles":["T","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1206753666"},{"id":"rs1797156147","seq_region_name":"7","clinical_significance":[],"start":140551952,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140551952,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"start":140551953,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140551953,"alleles":["C","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797156256","clinical_significance":[]},{"start":140551954,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140551954,"alleles":["A","C"],"strand":1,"feature_type":"variation","id":"rs1482000592","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs974393499","seq_region_name":"7","end":140551956,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140551956,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs10227057","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551963,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140551963},{"seq_region_name":"7","id":"rs75820657","clinical_significance":[],"start":140551966,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140551966,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1585610275","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551967,"source":"dbSNP","strand":1,"feature_type":"variation","end":140551967,"alleles":["G","A","T"]},{"end":140551968,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140551968,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1797156908","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551971,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140551971,"seq_region_name":"7","id":"rs1797157031","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140551980,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551980,"source":"dbSNP","id":"rs1797157151","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1797157258","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551981,"feature_type":"variation","strand":1,"alleles":["T","TT"],"end":140551981},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551983,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140551983,"seq_region_name":"7","id":"rs1585610290","clinical_significance":[]},{"source":"dbSNP","start":140551989,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140551989,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1042259133"},{"id":"rs2130545231","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140551990,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140551990,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551993,"feature_type":"variation","strand":1,"end":140551993,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1797157587"},{"clinical_significance":[],"id":"rs1797157685","seq_region_name":"7","source":"dbSNP","start":140551994,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140551994,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797157787","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140551996,"feature_type":"variation","strand":1,"end":140551996,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs890929034","source":"dbSNP","start":140552002,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140552002,"alleles":["T","G"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140552003,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552003,"clinical_significance":[],"seq_region_name":"7","id":"rs1797157993"},{"seq_region_name":"7","id":"rs1336649465","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552006,"source":"dbSNP","strand":1,"feature_type":"variation","end":140552006,"alleles":["A","G"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552010,"source":"dbSNP","strand":1,"feature_type":"variation","end":140552010,"alleles":["G","A","C"],"seq_region_name":"7","id":"rs150399762","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797158419","alleles":["T","C"],"end":140552018,"feature_type":"variation","strand":1,"source":"dbSNP","start":140552018,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1039583360","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140552020,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552020,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1412420596","seq_region_name":"7","source":"dbSNP","start":140552021,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140552021,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1407383803","alleles":["T","C"],"end":140552027,"feature_type":"variation","strand":1,"source":"dbSNP","start":140552027,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs748775651","clinical_significance":[],"start":140552034,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140552034,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"id":"rs1797159021","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552035,"source":"dbSNP","strand":1,"feature_type":"variation","end":140552035,"alleles":["C","T"]},{"start":140552037,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140552037,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1388998604","clinical_significance":[]},{"alleles":["C","T"],"end":140552038,"feature_type":"variation","strand":1,"source":"dbSNP","start":140552038,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1163081733","seq_region_name":"7"},{"start":140552040,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140552040,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1056322370","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797159440","feature_type":"variation","strand":1,"alleles":["A","T"],"end":140552045,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552045},{"feature_type":"variation","strand":1,"end":140552048,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552048,"clinical_significance":[],"id":"rs1797159567","seq_region_name":"7"},{"id":"rs1797159670","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552053,"source":"dbSNP","strand":1,"feature_type":"variation","end":140552053,"alleles":["C","A"]},{"seq_region_name":"7","id":"rs770470206","clinical_significance":[],"end":140552058,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140552058,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552059,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140552059,"clinical_significance":[],"seq_region_name":"7","id":"rs895051483"},{"alleles":["C","-"],"end":140552061,"feature_type":"variation","strand":1,"source":"dbSNP","start":140552061,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1183630620"},{"seq_region_name":"7","id":"rs996184676","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552062,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140552062},{"end":140552063,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140552063,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797160241","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140552069,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552069,"clinical_significance":[],"seq_region_name":"7","id":"rs1585610491"},{"clinical_significance":[],"id":"rs138177443","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","A"],"end":140552071,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552071},{"seq_region_name":"7","id":"rs893207949","clinical_significance":[],"start":140552075,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140552075,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797160957","source":"dbSNP","start":140552076,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140552076,"alleles":["T","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1797161118","clinical_significance":[],"start":140552079,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140552079,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"end":140552080,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140552080,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1222192418"},{"seq_region_name":"7","id":"rs1563134783","clinical_significance":[],"end":140552087,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140552087,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1797161538","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552097,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140552097},{"strand":1,"feature_type":"variation","end":140552100,"alleles":["C","A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552100,"source":"dbSNP","seq_region_name":"7","id":"rs556658803","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs574760786","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140552101,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552101},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130545500","end":140552106,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140552106,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130545515","alleles":["A","G"],"end":140552108,"feature_type":"variation","strand":1,"source":"dbSNP","start":140552108,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140552111,"alleles":["G","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552111,"clinical_significance":[],"seq_region_name":"7","id":"rs1401063958"},{"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140552115,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552115,"source":"dbSNP","seq_region_name":"7","id":"rs1038329626","clinical_significance":[]},{"start":140552116,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140552116,"strand":1,"feature_type":"variation","id":"rs1797162140","seq_region_name":"7","clinical_significance":[]},{"start":140552120,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140552120,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797162242","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552121,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140552121,"id":"rs898611967","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552122,"feature_type":"variation","strand":1,"end":140552122,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs994669978"},{"clinical_significance":[],"id":"rs1020479862","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552125,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140552125},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140552126,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552126,"clinical_significance":[],"seq_region_name":"7","id":"rs1585610645"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1025689493","source":"dbSNP","start":140552128,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140552128,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["A","-"],"end":140552129,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552129,"clinical_significance":[],"seq_region_name":"7","id":"rs1246597918"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797163368","end":140552130,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140552130,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140552133,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552133,"source":"dbSNP","id":"rs1797163546","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552136,"feature_type":"variation","strand":1,"end":140552136,"alleles":["A","G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs142836911"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552139,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140552139,"id":"rs1797163945","seq_region_name":"7","clinical_significance":[]},{"id":"rs2130545633","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140552141,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552141,"source":"dbSNP"},{"seq_region_name":"7","id":"rs2130545648","clinical_significance":[],"start":140552142,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140552142,"strand":1,"feature_type":"variation"},{"end":140552144,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140552144,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs982106598","clinical_significance":[]},{"source":"dbSNP","start":140552147,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140552147,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130545672"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552149,"source":"dbSNP","strand":1,"feature_type":"variation","end":140552149,"alleles":["A","G"],"seq_region_name":"7","id":"rs2130545682","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552150,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140552150,"seq_region_name":"7","id":"rs2130545695","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1034597295","alleles":["A","C","G","T"],"end":140552151,"feature_type":"variation","strand":1,"source":"dbSNP","start":140552151,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1329926228","source":"dbSNP","start":140552157,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140552157,"alleles":["G","A"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552163,"feature_type":"variation","strand":1,"alleles":["CC","C"],"end":140552164,"clinical_significance":[],"seq_region_name":"7","id":"rs964270811"},{"source":"dbSNP","start":140552166,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140552166,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797164312"},{"seq_region_name":"7","id":"rs1401656383","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140552171,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552171,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140552175,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552175,"source":"dbSNP","seq_region_name":"7","id":"rs192303056","clinical_significance":[]},{"seq_region_name":"7","id":"rs1021962511","clinical_significance":[],"strand":1,"feature_type":"variation","end":140552180,"alleles":["CCTA","CCTACCTA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552177,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1797164800","seq_region_name":"7","end":140552181,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140552181,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140552183,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552183,"clinical_significance":[],"seq_region_name":"7","id":"rs1455364179"},{"seq_region_name":"7","id":"rs1410546643","clinical_significance":[],"strand":1,"feature_type":"variation","end":140552189,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552189,"source":"dbSNP"},{"id":"rs1797165147","seq_region_name":"7","clinical_significance":[],"start":140552194,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140552194,"alleles":["T","G"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140552198,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552198,"clinical_significance":[],"seq_region_name":"7","id":"rs1797165260"},{"seq_region_name":"7","id":"rs1191342016","clinical_significance":[],"start":140552204,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140552204,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"end":140552206,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140552206,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1347321157","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797165602","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140552209,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552209},{"clinical_significance":[],"seq_region_name":"7","id":"rs1217691016","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552210,"feature_type":"variation","strand":1,"end":140552210,"alleles":["C","G","T"]},{"seq_region_name":"7","id":"rs1279959486","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552212,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140552212},{"end":140552213,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140552213,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs572749454"},{"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140552215,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552215,"source":"dbSNP","seq_region_name":"7","id":"rs1797166095","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140552227,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552227,"clinical_significance":[],"seq_region_name":"7","id":"rs1354128082"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797166344","alleles":["C","T"],"end":140552232,"feature_type":"variation","strand":1,"source":"dbSNP","start":140552232,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797166449","alleles":["G","T"],"end":140552234,"feature_type":"variation","strand":1,"source":"dbSNP","start":140552234,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1270191959","feature_type":"variation","strand":1,"alleles":["G","C","T"],"end":140552235,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552235},{"clinical_significance":[],"seq_region_name":"7","id":"rs1207032712","source":"dbSNP","start":140552236,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140552236,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1797166786","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["GGAGGGGAGGGGAG","GGAGGGGAG"],"end":140552250,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552237},{"strand":1,"feature_type":"variation","end":140552240,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552240,"source":"dbSNP","id":"rs759915314","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552244,"source":"dbSNP","strand":1,"feature_type":"variation","end":140552244,"alleles":["A","T"],"seq_region_name":"7","id":"rs967700070","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797167128","clinical_significance":[],"start":140552246,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140552246,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1279417377","source":"dbSNP","start":140552247,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140552247,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140552252,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140552252,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797167347"},{"seq_region_name":"7","id":"rs1221071100","clinical_significance":[],"end":140552257,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140552257,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs565741316","clinical_significance":[],"strand":1,"feature_type":"variation","end":140552258,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552258,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552261,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140552261,"clinical_significance":[],"seq_region_name":"7","id":"rs1797167652"},{"seq_region_name":"7","id":"rs1797167760","clinical_significance":[],"start":140552270,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140552270,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs973744291","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552273,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140552273},{"clinical_significance":[],"id":"rs1797167957","seq_region_name":"7","feature_type":"variation","strand":1,"end":140552273,"alleles":["-","TA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552274},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797168069","source":"dbSNP","start":140552275,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140552275,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140552277,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","AA"],"end":140552277,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs35824631"},{"feature_type":"variation","strand":1,"end":140552280,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552280,"clinical_significance":[],"seq_region_name":"7","id":"rs1274810005"},{"clinical_significance":[],"seq_region_name":"7","id":"rs923685217","feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140552281,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552281},{"clinical_significance":[],"seq_region_name":"7","id":"rs1367768851","source":"dbSNP","start":140552282,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140552282,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140552283,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140552283,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1387532863"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552283,"feature_type":"variation","strand":1,"alleles":["TTTCTTTCTTTCTTT","TTTCTTTCTTT","TTTCTTTCTTTCTTTCTTT"],"end":140552297,"clinical_significance":[],"seq_region_name":"7","id":"rs1319014747"},{"clinical_significance":[],"id":"rs1797168889","seq_region_name":"7","end":140552285,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140552285,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs939209762","alleles":["C","T"],"end":140552286,"feature_type":"variation","strand":1,"source":"dbSNP","start":140552286,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552287,"source":"dbSNP","strand":1,"feature_type":"variation","end":140552287,"alleles":["T","C"],"seq_region_name":"7","id":"rs991933292","clinical_significance":[]},{"clinical_significance":[],"id":"rs1422923271","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552294,"feature_type":"variation","strand":1,"end":140552294,"alleles":["C","A"]},{"end":140552299,"alleles":["TTTTT","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140552295,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1260894209"},{"start":140552299,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140552305,"alleles":["TCTCTCT","TCT","TCTCT"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs773579156","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1186513385","source":"dbSNP","start":140552302,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140552302,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1797169686","seq_region_name":"7","end":140552303,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140552303,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140552305,"alleles":["T","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552305,"source":"dbSNP","id":"rs1797169805","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1797169931","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552308,"feature_type":"variation","strand":1,"end":140552308,"alleles":["T","G"]},{"alleles":["T","C"],"end":140552309,"strand":1,"feature_type":"variation","start":140552309,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs947963271","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797170161","clinical_significance":[],"end":140552312,"alleles":["CCC","CCCC"],"strand":1,"feature_type":"variation","start":140552310,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs772651481","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552313,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140552313},{"seq_region_name":"7","id":"rs1238274439","clinical_significance":[],"start":140552315,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140552315,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552316,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140552316,"clinical_significance":[],"id":"rs1038215331","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1212280958","clinical_significance":[],"alleles":["T","C"],"end":140552322,"strand":1,"feature_type":"variation","start":140552322,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs116201438","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552323,"source":"dbSNP","strand":1,"feature_type":"variation","end":140552323,"alleles":["T","G"]},{"source":"dbSNP","start":140552324,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140552324,"alleles":["T","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs929971487"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585611082","source":"dbSNP","start":140552326,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140552326,"alleles":["C","T"],"feature_type":"variation","strand":1},{"start":140552326,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["CCTTCCTTCCTT","CCTTCCTT"],"end":140552337,"strand":1,"feature_type":"variation","id":"rs1229754781","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs564376426","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552328,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140552328},{"seq_region_name":"7","id":"rs982472712","clinical_significance":[],"strand":1,"feature_type":"variation","end":140552330,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552330,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["CCTTCCTTTCCCTCTCTCTCTCCCTTCCT","CCTTCCTTTCCCTCTCTCTCTCCCTTCCTTTCCCTCTCTCTCTCCCTTCCT"],"end":140552358,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552330,"source":"dbSNP","seq_region_name":"7","id":"rs1563134921","clinical_significance":[]},{"alleles":["T","C"],"end":140552337,"feature_type":"variation","strand":1,"source":"dbSNP","start":140552337,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1228148078"},{"alleles":["C","A"],"end":140552339,"strand":1,"feature_type":"variation","start":140552339,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs775646451","clinical_significance":[]},{"end":140552351,"alleles":["CTCTCTCTCTC","CTCTCTC","CTCTCTCTC","CTCTCTCTCTCTC"],"strand":1,"feature_type":"variation","start":140552341,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs560033744","clinical_significance":[]},{"start":140552343,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140552343,"alleles":["C","A"],"strand":1,"feature_type":"variation","id":"rs1356906219","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs912397349","seq_region_name":"7","alleles":["T","A"],"end":140552344,"feature_type":"variation","strand":1,"source":"dbSNP","start":140552344,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140552345,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140552345,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs761165156"},{"clinical_significance":[],"id":"rs1797172280","seq_region_name":"7","alleles":["CTCTCTCCCTTCCTCCCTCCCTCTC","CTCTCTCCCTTCCTCCCTCCCTCTCTCCCTTCCTCCCTCCCTCTC"],"end":140552369,"feature_type":"variation","strand":1,"source":"dbSNP","start":140552345,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1392011362","clinical_significance":[],"strand":1,"feature_type":"variation","end":140552347,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552347,"source":"dbSNP"},{"start":140552350,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140552350,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs112193187","clinical_significance":[]},{"clinical_significance":[],"id":"rs1448679724","seq_region_name":"7","source":"dbSNP","start":140552353,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140552353,"alleles":["C","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs899746841","seq_region_name":"7","source":"dbSNP","start":140552355,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140552355,"feature_type":"variation","strand":1},{"alleles":["C","A"],"end":140552361,"feature_type":"variation","strand":1,"source":"dbSNP","start":140552361,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797172884"},{"clinical_significance":[],"seq_region_name":"7","id":"rs764395300","source":"dbSNP","start":140552365,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140552365,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140552367,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140552367,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1054449529"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1183796872","feature_type":"variation","strand":1,"end":140552371,"alleles":["CCC","CC"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552369},{"strand":1,"feature_type":"variation","end":140552376,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552376,"source":"dbSNP","seq_region_name":"7","id":"rs1482423725","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585611265","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552380,"source":"dbSNP","strand":1,"feature_type":"variation","end":140552382,"alleles":["CCC","CC"]},{"seq_region_name":"7","id":"rs1018451448","clinical_significance":[],"strand":1,"feature_type":"variation","end":140552382,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552382,"source":"dbSNP"},{"source":"dbSNP","start":140552385,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140552385,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797173619"},{"end":140552394,"alleles":["CTTCTTCTT","CTTCTT"],"strand":1,"feature_type":"variation","start":140552386,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1206036421","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797173827","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552390,"feature_type":"variation","strand":1,"end":140552399,"alleles":["TTCTTTCTTT","TTCTTT"]},{"feature_type":"variation","strand":1,"end":140552393,"alleles":["TCT","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552391,"clinical_significance":[],"seq_region_name":"7","id":"rs1484291414"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797174034","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552393,"feature_type":"variation","strand":1,"end":140552395,"alleles":["TTT","-"]},{"end":140552394,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140552394,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1273109620"},{"feature_type":"variation","strand":1,"end":140552401,"alleles":["TTTTT","TTTT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552397,"clinical_significance":[],"seq_region_name":"7","id":"rs1380591112"},{"clinical_significance":[],"seq_region_name":"7","id":"rs900120033","source":"dbSNP","start":140552399,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140552399,"alleles":["T","C"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552401,"feature_type":"variation","strand":1,"end":140552401,"alleles":["T","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs543925846"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552402,"source":"dbSNP","strand":1,"feature_type":"variation","end":140552402,"alleles":["C","A"],"seq_region_name":"7","id":"rs1011844720","clinical_significance":[]},{"id":"rs1797174943","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["TTT","TTTT"],"end":140552414,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552412,"source":"dbSNP"},{"source":"dbSNP","start":140552418,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140552418,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797175084"},{"strand":1,"feature_type":"variation","end":140552420,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552420,"source":"dbSNP","seq_region_name":"7","id":"rs1229643643","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552422,"feature_type":"variation","strand":1,"end":140552422,"alleles":["C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs893114658"},{"alleles":["A","G"],"end":140552425,"feature_type":"variation","strand":1,"source":"dbSNP","start":140552425,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797175588"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552427,"feature_type":"variation","strand":1,"end":140552427,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1160869234"},{"alleles":["C","G"],"end":140552434,"strand":1,"feature_type":"variation","start":140552434,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1010344764","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1376600923","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552441,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140552441},{"clinical_significance":[],"seq_region_name":"7","id":"rs1292117988","source":"dbSNP","start":140552444,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C","G"],"end":140552444,"feature_type":"variation","strand":1},{"end":140552445,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140552445,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797176478"},{"seq_region_name":"7","id":"rs1797176673","clinical_significance":[],"start":140552447,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140552447,"strand":1,"feature_type":"variation"},{"alleles":["A","C"],"end":140552449,"strand":1,"feature_type":"variation","start":140552449,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1797176856","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797177017","clinical_significance":[],"alleles":["G","C","T"],"end":140552453,"strand":1,"feature_type":"variation","start":140552453,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1797177212","clinical_significance":[],"end":140552455,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140552455,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140552459,"alleles":["A","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552459,"source":"dbSNP","seq_region_name":"7","id":"rs1409917265","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797177603","clinical_significance":[],"alleles":["T","A"],"end":140552462,"strand":1,"feature_type":"variation","start":140552462,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1585611422","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140552464,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552464,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797177806","source":"dbSNP","start":140552466,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140552466,"alleles":["T","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1383391571","feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140552467,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552467},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140552468,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552468,"clinical_significance":[],"id":"rs1400662668","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs146102808","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552472,"feature_type":"variation","strand":1,"end":140552472,"alleles":["C","A"]},{"end":140552473,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140552473,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1350221489","seq_region_name":"7"},{"source":"dbSNP","start":140552475,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140552475,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs907380788"},{"clinical_significance":[],"seq_region_name":"7","id":"rs368096559","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552478,"feature_type":"variation","strand":1,"end":140552478,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797178567","source":"dbSNP","start":140552479,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140552479,"alleles":["A","C"],"feature_type":"variation","strand":1},{"id":"rs1797178672","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140552481,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552481,"source":"dbSNP"},{"id":"rs761951277","seq_region_name":"7","clinical_significance":[],"start":140552484,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140552484,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552486,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140552486,"clinical_significance":[],"seq_region_name":"7","id":"rs1797178882"},{"source":"dbSNP","start":140552496,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140552496,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1302920948"},{"alleles":["A","G"],"end":140552498,"strand":1,"feature_type":"variation","start":140552498,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs958971086","clinical_significance":[]},{"start":140552504,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140552504,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs28653484","clinical_significance":[]},{"clinical_significance":[],"id":"rs113074427","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552505,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140552505},{"clinical_significance":[],"id":"rs951011112","seq_region_name":"7","feature_type":"variation","strand":1,"end":140552506,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552506},{"end":140552508,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140552508,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs754814384","clinical_significance":[]},{"clinical_significance":[],"id":"rs1563135068","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552509,"feature_type":"variation","strand":1,"end":140552509,"alleles":["G","A","C"]},{"start":140552510,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140552510,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585611570","clinical_significance":[]},{"start":140552510,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["CTCAGCCTC","CTC"],"end":140552518,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs991985746","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140552514,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552514,"clinical_significance":[],"id":"rs1349793483","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1210365957","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552517,"feature_type":"variation","strand":1,"end":140552517,"alleles":["T","A"]},{"clinical_significance":[],"id":"rs1797180363","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140552523,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552523},{"id":"rs1797180489","seq_region_name":"7","clinical_significance":[],"alleles":["G","C"],"end":140552526,"strand":1,"feature_type":"variation","start":140552526,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs916421382","alleles":["C","G"],"end":140552527,"feature_type":"variation","strand":1,"source":"dbSNP","start":140552527,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1797180720","clinical_significance":[],"alleles":["G","A","T"],"end":140552530,"strand":1,"feature_type":"variation","start":140552530,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140552531,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140552531,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs969156646","clinical_significance":[]},{"seq_region_name":"7","id":"rs912305156","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552533,"source":"dbSNP","strand":1,"feature_type":"variation","end":140552533,"alleles":["C","G"]},{"seq_region_name":"7","id":"rs527612434","clinical_significance":[],"alleles":["C","T"],"end":140552536,"strand":1,"feature_type":"variation","start":140552536,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797181230","end":140552537,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140552537,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140552540,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140552540,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs552483863"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130546828","alleles":["CACAC","CAC"],"end":140552546,"feature_type":"variation","strand":1,"source":"dbSNP","start":140552542,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140552552,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552552,"source":"dbSNP","seq_region_name":"7","id":"rs1797181436","clinical_significance":[]},{"end":140552558,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140552558,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130546840"},{"clinical_significance":[],"seq_region_name":"7","id":"rs919827933","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140552562,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552562},{"seq_region_name":"7","id":"rs1797182011","clinical_significance":[],"alleles":["TTTTTTT","TTTTTT","TTTTTTTT"],"end":140552569,"strand":1,"feature_type":"variation","start":140552563,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1351774798","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552569,"source":"dbSNP","strand":1,"feature_type":"variation","end":140552569,"alleles":["T","C","G"]},{"start":140552572,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140552572,"alleles":["A","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1285960170","clinical_significance":[]},{"id":"rs766831216","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["TTTTTT","TTTTTTT"],"end":140552578,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552573,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140552574,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552574,"source":"dbSNP","id":"rs1585611681","seq_region_name":"7","clinical_significance":[]},{"end":140552579,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140552579,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs965628564","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs536220730","alleles":["G","C"],"end":140552582,"feature_type":"variation","strand":1,"source":"dbSNP","start":140552582,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140552585,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552585,"source":"dbSNP","seq_region_name":"7","id":"rs1295016070","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1047040228","source":"dbSNP","start":140552587,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140552587,"alleles":["A","G"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552590,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140552590,"clinical_significance":[],"seq_region_name":"7","id":"rs1349471976"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552598,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140552598,"seq_region_name":"7","id":"rs1160207639","clinical_significance":[]},{"clinical_significance":[],"id":"rs912678272","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552603,"feature_type":"variation","strand":1,"end":140552603,"alleles":["G","A"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552605,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140552605,"id":"rs1646783398","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552611,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140552611,"clinical_significance":[],"id":"rs187913420","seq_region_name":"7"},{"start":140552612,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140552612,"alleles":["G","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797183509","clinical_significance":[]},{"start":140552614,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140552614,"strand":1,"feature_type":"variation","id":"rs921210384","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","T"],"end":140552618,"strand":1,"feature_type":"variation","start":140552618,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs936616144","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552622,"source":"dbSNP","strand":1,"feature_type":"variation","end":140552625,"alleles":["TCGT","T"],"seq_region_name":"7","id":"rs1797183833","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1054091037","alleles":["C","T"],"end":140552623,"feature_type":"variation","strand":1,"source":"dbSNP","start":140552623,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1180850472","clinical_significance":[],"strand":1,"feature_type":"variation","end":140552624,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552624,"source":"dbSNP"},{"source":"dbSNP","start":140552626,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140552626,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797184288"},{"clinical_significance":[],"seq_region_name":"7","id":"rs142116055","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552627,"feature_type":"variation","strand":1,"end":140552627,"alleles":["G","A"]},{"clinical_significance":[],"id":"rs1470004502","seq_region_name":"7","feature_type":"variation","strand":1,"end":140552633,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552633},{"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140552636,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552636,"source":"dbSNP","seq_region_name":"7","id":"rs945998767","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585611904","clinical_significance":[],"start":140552637,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140552637,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1393572803","clinical_significance":[],"alleles":["T","C"],"end":140552641,"strand":1,"feature_type":"variation","start":140552641,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140552644,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140552644,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1043730807","clinical_significance":[]},{"start":140552646,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140552646,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797185140","clinical_significance":[]},{"start":140552650,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140552650,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797185244","clinical_significance":[]},{"clinical_significance":[],"id":"rs1265685098","seq_region_name":"7","source":"dbSNP","start":140552656,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140552656,"feature_type":"variation","strand":1},{"id":"rs1797185481","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552658,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140552658},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797185590","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552660,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140552660},{"clinical_significance":[],"id":"rs1237725987","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552661,"feature_type":"variation","strand":1,"end":140552661,"alleles":["G","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552663,"source":"dbSNP","strand":1,"feature_type":"variation","end":140552663,"alleles":["A","G"],"id":"rs903417498","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140552664,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552664,"clinical_significance":[],"id":"rs555062511","seq_region_name":"7"},{"end":140552673,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140552673,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs144788307"},{"id":"rs1797186062","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140552675,"strand":1,"feature_type":"variation","start":140552675,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["C","G"],"end":140552676,"feature_type":"variation","strand":1,"source":"dbSNP","start":140552676,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs28707559"},{"id":"rs1563135193","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["TGTG","TG"],"end":140552680,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552677,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797186412","source":"dbSNP","start":140552678,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140552678,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1401239212","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552679,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140552679},{"clinical_significance":[],"id":"rs1321020280","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552680,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140552680},{"alleles":["G","A"],"end":140552682,"feature_type":"variation","strand":1,"source":"dbSNP","start":140552682,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1797186787","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552687,"feature_type":"variation","strand":1,"end":140552687,"alleles":["T","C"],"clinical_significance":[],"id":"rs1437538729","seq_region_name":"7"},{"id":"rs1563135208","seq_region_name":"7","clinical_significance":[],"end":140552689,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140552689,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140552690,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552690,"source":"dbSNP","seq_region_name":"7","id":"rs1797187115","clinical_significance":[]},{"clinical_significance":[],"id":"rs1449294322","seq_region_name":"7","source":"dbSNP","start":140552691,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140552691,"feature_type":"variation","strand":1},{"alleles":["G","C"],"end":140552695,"feature_type":"variation","strand":1,"source":"dbSNP","start":140552695,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs755986982"},{"alleles":["C","A"],"end":140552696,"strand":1,"feature_type":"variation","start":140552696,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1013290046","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552697,"feature_type":"variation","strand":1,"end":140552697,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1466620138"},{"feature_type":"variation","strand":1,"end":140552702,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552702,"clinical_significance":[],"seq_region_name":"7","id":"rs1379838268"},{"start":140552703,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140552703,"alleles":["T","G"],"strand":1,"feature_type":"variation","id":"rs1797187778","seq_region_name":"7","clinical_significance":[]},{"start":140552707,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C","T"],"end":140552707,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs4725750","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552713,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140552713,"seq_region_name":"7","id":"rs1433157127","clinical_significance":[]},{"alleles":["T","C"],"end":140552721,"strand":1,"feature_type":"variation","start":140552721,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797188624","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797188776","clinical_significance":[],"start":140552728,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140552728,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140552730,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140552730,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797188942"},{"strand":1,"feature_type":"variation","alleles":["GGG","GGGG"],"end":140552732,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552730,"source":"dbSNP","seq_region_name":"7","id":"rs1797189110","clinical_significance":[]},{"source":"dbSNP","start":140552732,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140552732,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1245319652"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1729164646","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552737,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140552737},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797189438","alleles":["T","G"],"end":140552742,"feature_type":"variation","strand":1,"source":"dbSNP","start":140552742,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1465932170","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552742,"source":"dbSNP","strand":1,"feature_type":"variation","end":140552745,"alleles":["TTTT","TTT"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs894610747","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140552748,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552748},{"seq_region_name":"7","id":"rs969208676","clinical_significance":[],"strand":1,"feature_type":"variation","end":140552755,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552755,"source":"dbSNP"},{"end":140552756,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140552756,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1204000075","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552757,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140552757,"clinical_significance":[],"id":"rs1797190031","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552758,"source":"dbSNP","strand":1,"feature_type":"variation","end":140552758,"alleles":["T","G"],"seq_region_name":"7","id":"rs1285859044","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552761,"source":"dbSNP","strand":1,"feature_type":"variation","end":140552761,"alleles":["A","G"],"id":"rs1797190236","seq_region_name":"7","clinical_significance":[]},{"id":"rs1257294358","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140552765,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552765,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1230931311","clinical_significance":[],"start":140552767,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","AA"],"end":140552767,"strand":1,"feature_type":"variation"},{"start":140552768,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140552768,"alleles":["C","A","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs995775009","clinical_significance":[]},{"start":140552769,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140552769,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs368252974","clinical_significance":[]},{"start":140552774,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140552774,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs951085604","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1258173374","feature_type":"variation","strand":1,"end":140552776,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552776},{"seq_region_name":"7","id":"rs1797191046","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["TCACCACAGCCTCGA","-"],"end":140552792,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552778,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585612252","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552779,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140552779},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552780,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140552780,"clinical_significance":[],"seq_region_name":"7","id":"rs1797191234"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140552782,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552782,"source":"dbSNP","seq_region_name":"7","id":"rs1458776738","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552783,"source":"dbSNP","strand":1,"feature_type":"variation","end":140552783,"alleles":["A","G"],"seq_region_name":"7","id":"rs1797191446","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1396879708","alleles":["G","A"],"end":140552791,"feature_type":"variation","strand":1,"source":"dbSNP","start":140552791,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140552794,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140552794,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs554168191","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140552796,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552796,"clinical_significance":[],"seq_region_name":"7","id":"rs1301240773"},{"id":"rs1797192172","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140552797,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552797,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1797192347","clinical_significance":[],"start":140552803,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140552803,"strand":1,"feature_type":"variation"},{"alleles":["A","G"],"end":140552806,"feature_type":"variation","strand":1,"source":"dbSNP","start":140552806,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs951327469"},{"feature_type":"variation","strand":1,"end":140552812,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552812,"clinical_significance":[],"id":"rs1196359299","seq_region_name":"7"},{"end":140552814,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140552814,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1797192869","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140552815,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552815,"source":"dbSNP","seq_region_name":"7","id":"rs1003832353","clinical_significance":[]},{"alleles":["T","G"],"end":140552816,"strand":1,"feature_type":"variation","start":140552816,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797193192","clinical_significance":[]},{"source":"dbSNP","start":140552817,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140552817,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797193357"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552820,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140552820,"clinical_significance":[],"id":"rs983223256","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs912573760","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552821,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140552821},{"clinical_significance":[],"id":"rs1797193879","seq_region_name":"7","alleles":["A","G"],"end":140552823,"feature_type":"variation","strand":1,"source":"dbSNP","start":140552823,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140552825,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140552825,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs943982176"},{"id":"rs1039822496","seq_region_name":"7","clinical_significance":[],"start":140552829,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140552829,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs55939812","source":"dbSNP","start":140552837,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140552837,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140552839,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140552845,"alleles":["ATTAATT","ATT"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797194409"},{"seq_region_name":"7","id":"rs2130547625","clinical_significance":[],"strand":1,"feature_type":"variation","end":140552851,"alleles":["TTCTTTCT","TTCT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552844,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797194512","source":"dbSNP","start":140552854,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140552854,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1198286348","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140552856,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552856,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140552861,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552861,"clinical_significance":[],"id":"rs1485270182","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140552862,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552862,"clinical_significance":[],"seq_region_name":"7","id":"rs34651797"},{"source":"dbSNP","start":140552863,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140552863,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1206980368"},{"clinical_significance":[],"id":"rs1339832176","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552864,"feature_type":"variation","strand":1,"end":140552864,"alleles":["G","-"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552865,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140552865,"seq_region_name":"7","id":"rs1269420353","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552870,"feature_type":"variation","strand":1,"end":140552870,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1245792208"},{"start":140552875,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140552875,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797195406","clinical_significance":[]},{"alleles":["C","T"],"end":140552882,"feature_type":"variation","strand":1,"source":"dbSNP","start":140552882,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797195516"},{"seq_region_name":"7","id":"rs1342552095","clinical_significance":[],"end":140552884,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140552884,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1797195739","clinical_significance":[],"start":140552887,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140552887,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1043225362","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140552894,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552894,"source":"dbSNP"},{"source":"dbSNP","start":140552895,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140552895,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1414254174"},{"end":140552896,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140552896,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1370662815","clinical_significance":[]},{"source":"dbSNP","start":140552898,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140552898,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1371674111"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552899,"source":"dbSNP","strand":1,"feature_type":"variation","end":140552899,"alleles":["C","G"],"id":"rs558003117","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs79637340","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552901,"source":"dbSNP","strand":1,"feature_type":"variation","end":140552901,"alleles":["A","G"]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140552904,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552904,"clinical_significance":[],"seq_region_name":"7","id":"rs1424431237"},{"end":140552906,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140552906,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797196648"},{"clinical_significance":[],"id":"rs1396183300","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140552909,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552909},{"id":"rs148217097","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140552912,"alleles":["AA","AAAAAA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552911,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552918,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140552918,"seq_region_name":"7","id":"rs543569228","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140552919,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552919,"source":"dbSNP","id":"rs2130547825","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552920,"feature_type":"variation","strand":1,"end":140552920,"alleles":["T","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs561672017"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797197295","alleles":["T","C"],"end":140552926,"feature_type":"variation","strand":1,"source":"dbSNP","start":140552926,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552936,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140552936,"id":"rs1396106449","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130547851","end":140552941,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140552941,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140552942,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552942,"clinical_significance":[],"seq_region_name":"7","id":"rs1797197540"},{"seq_region_name":"7","id":"rs1057494532","clinical_significance":[],"strand":1,"feature_type":"variation","end":140552944,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552944,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1185067016","source":"dbSNP","start":140552952,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140552952,"feature_type":"variation","strand":1},{"alleles":["A","G"],"end":140552955,"strand":1,"feature_type":"variation","start":140552955,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1474611948","seq_region_name":"7","clinical_significance":[]},{"end":140552957,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140552957,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1563135385","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs778340142","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552963,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140552963},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140552966,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552966,"source":"dbSNP","seq_region_name":"7","id":"rs1585612594","clinical_significance":[]},{"seq_region_name":"7","id":"rs896175852","clinical_significance":[],"start":140552967,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140552967,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552968,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140552968,"clinical_significance":[],"id":"rs1335975703","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1013179158","clinical_significance":[],"start":140552969,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140552969,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1585612626","clinical_significance":[],"start":140552972,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140552972,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1210228641","alleles":["G","T"],"end":140552973,"feature_type":"variation","strand":1,"source":"dbSNP","start":140552973,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1358659055","clinical_significance":[],"start":140552974,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140552974,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1232702731","clinical_significance":[],"end":140552979,"alleles":["A","-"],"strand":1,"feature_type":"variation","start":140552979,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797199007","source":"dbSNP","start":140552979,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140552979,"alleles":["A","C"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552979,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AGGGGTGAAGGGGTG","AGGGGTGAAGGGGTGAAGGGGTG"],"end":140552993,"seq_region_name":"7","id":"rs1263935230","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552980,"source":"dbSNP","strand":1,"feature_type":"variation","end":140552980,"alleles":["G","A"],"seq_region_name":"7","id":"rs1290331593","clinical_significance":[]},{"seq_region_name":"7","id":"rs1351162531","clinical_significance":[],"strand":1,"feature_type":"variation","end":140552983,"alleles":["GGGG","GGG"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552980,"source":"dbSNP"},{"seq_region_name":"7","id":"rs115888080","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140552983,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552983,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797199715","end":140552988,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140552988,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797199808","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140552989,"feature_type":"variation","strand":1,"end":140552989,"alleles":["G","A"]},{"alleles":["G","A","T"],"end":140552990,"strand":1,"feature_type":"variation","start":140552990,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1797199928","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1797200060","seq_region_name":"7","alleles":["G","T"],"end":140552991,"feature_type":"variation","strand":1,"source":"dbSNP","start":140552991,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552992,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140552992,"seq_region_name":"7","id":"rs1563135420","clinical_significance":[]},{"seq_region_name":"7","id":"rs1232618094","clinical_significance":[],"strand":1,"feature_type":"variation","end":140552997,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140552997,"source":"dbSNP"},{"alleles":["C","T"],"end":140553001,"feature_type":"variation","strand":1,"source":"dbSNP","start":140553001,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs574522321"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553002,"source":"dbSNP","strand":1,"feature_type":"variation","end":140553002,"alleles":["C","T"],"seq_region_name":"7","id":"rs1797200682","clinical_significance":[]},{"id":"rs913804698","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140553004,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553004,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["CC","C"],"end":140553005,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553004,"source":"dbSNP","seq_region_name":"7","id":"rs1278205199","clinical_significance":[]},{"source":"dbSNP","start":140553005,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140553005,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1319368679","seq_region_name":"7"},{"clinical_significance":[],"id":"rs577119825","seq_region_name":"7","feature_type":"variation","strand":1,"end":140553006,"alleles":["A","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553006},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553008,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140553008,"clinical_significance":[],"seq_region_name":"7","id":"rs1797201326"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1250378084","source":"dbSNP","start":140553010,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140553010,"alleles":["C","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1026813156","source":"dbSNP","start":140553011,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C","G"],"end":140553011,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1041733859","clinical_significance":[],"start":140553014,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140553014,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1797201749","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553019,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140553019},{"clinical_significance":[],"seq_region_name":"7","id":"rs1345316396","feature_type":"variation","strand":1,"end":140553024,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553024},{"clinical_significance":[],"seq_region_name":"7","id":"rs1462803006","feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140553025,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553025},{"end":140553029,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140553029,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs951256573"},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140553030,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553030,"source":"dbSNP","id":"rs982723830","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs201008202","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553044,"feature_type":"variation","strand":1,"end":140553044,"alleles":["T","A","C","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1213261353","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553046,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140553046},{"feature_type":"variation","strand":1,"end":140553047,"alleles":["GG","GGG"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553046,"clinical_significance":[],"seq_region_name":"7","id":"rs1797202633"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553048,"source":"dbSNP","strand":1,"feature_type":"variation","end":140553048,"alleles":["A","G"],"seq_region_name":"7","id":"rs1797202758","clinical_significance":[]},{"id":"rs1797202863","seq_region_name":"7","clinical_significance":[],"end":140553053,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140553053,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs2130548238","seq_region_name":"7","clinical_significance":[],"alleles":["A","C"],"end":140553054,"strand":1,"feature_type":"variation","start":140553054,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553057,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140553057,"clinical_significance":[],"id":"rs1201340462","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1270082138","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553061,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140553061},{"clinical_significance":[],"id":"rs1258715919","seq_region_name":"7","alleles":["ACAGAGACA","ACA"],"end":140553069,"feature_type":"variation","strand":1,"source":"dbSNP","start":140553061,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140553063,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553063,"clinical_significance":[],"id":"rs1797203347","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553063,"source":"dbSNP","strand":1,"feature_type":"variation","end":140553067,"alleles":["AGAGA","AGA"],"seq_region_name":"7","id":"rs1484938275","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553064,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140553064,"clinical_significance":[],"seq_region_name":"7","id":"rs1797203565"},{"seq_region_name":"7","id":"rs1797203681","clinical_significance":[],"end":140553066,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140553066,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs2130548300","clinical_significance":[],"alleles":["A","T"],"end":140553067,"strand":1,"feature_type":"variation","start":140553067,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs201878262","alleles":["G","A","C"],"end":140553072,"feature_type":"variation","strand":1,"source":"dbSNP","start":140553072,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140553075,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140553075,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1019512481","clinical_significance":[]},{"start":140553076,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AGAGA","A"],"end":140553080,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797204050","clinical_significance":[]},{"alleles":["AGAAAGAAA","AGAAA"],"end":140553086,"feature_type":"variation","strand":1,"source":"dbSNP","start":140553078,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1478830994"},{"clinical_significance":[],"id":"rs1329688921","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553079,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140553079},{"id":"rs965398496","seq_region_name":"7","clinical_significance":[],"start":140553080,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140553080,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"end":140553082,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140553082,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs975392338","clinical_significance":[]},{"source":"dbSNP","start":140553087,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C","G"],"end":140553087,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797204655"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797204788","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553090,"feature_type":"variation","strand":1,"end":140553090,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1797204904","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553091,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140553091},{"clinical_significance":[],"seq_region_name":"7","id":"rs1388934913","source":"dbSNP","start":140553092,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140553092,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1372683981","clinical_significance":[],"end":140553093,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140553093,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140553094,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140553094,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs928594801","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140553097,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553097,"source":"dbSNP","seq_region_name":"7","id":"rs1797205365","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553098,"feature_type":"variation","strand":1,"end":140553098,"alleles":["A","C","G"],"clinical_significance":[],"id":"rs938784200","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130548440","source":"dbSNP","start":140553099,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140553101,"alleles":["GGG","GG"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140553104,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553104,"clinical_significance":[],"seq_region_name":"7","id":"rs1173065667"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553106,"source":"dbSNP","strand":1,"feature_type":"variation","end":140553106,"alleles":["A","T"],"seq_region_name":"7","id":"rs1056260485","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130548467","end":140553107,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140553107,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140553108,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553108,"source":"dbSNP","seq_region_name":"7","id":"rs1478988634","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140553109,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553109,"clinical_significance":[],"seq_region_name":"7","id":"rs894657495"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553114,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140553114,"clinical_significance":[],"seq_region_name":"7","id":"rs1393037052"},{"id":"rs560126699","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140553117,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553117,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1174057097","source":"dbSNP","start":140553119,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140553119,"alleles":["T","TT"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1797206345","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553121,"feature_type":"variation","strand":1,"end":140553121,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs184261633","alleles":["G","A"],"end":140553123,"feature_type":"variation","strand":1,"source":"dbSNP","start":140553123,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1465470425","feature_type":"variation","strand":1,"end":140553125,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553125},{"clinical_significance":[],"seq_region_name":"7","id":"rs1048650186","end":140553126,"alleles":["T","A","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140553126,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1797206836","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140553127,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553127},{"start":140553129,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140553129,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs887357798","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs934800433","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553130,"feature_type":"variation","strand":1,"alleles":["G","GG"],"end":140553130},{"id":"rs1003868268","seq_region_name":"7","clinical_significance":[],"start":140553130,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140553130,"alleles":["G","A","T"],"strand":1,"feature_type":"variation"},{"start":140553131,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140553131,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs1797207354","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797207455","clinical_significance":[],"end":140553132,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140553132,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553135,"source":"dbSNP","strand":1,"feature_type":"variation","end":140553135,"alleles":["C","A"],"seq_region_name":"7","id":"rs1221405960","clinical_significance":[]},{"source":"dbSNP","start":140553136,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140553136,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1797207641","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140553141,"alleles":["A","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553141,"source":"dbSNP","seq_region_name":"7","id":"rs1019246562","clinical_significance":[]},{"alleles":["C","G"],"end":140553147,"feature_type":"variation","strand":1,"source":"dbSNP","start":140553147,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs900794589"},{"seq_region_name":"7","id":"rs1797208035","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553150,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140553150},{"source":"dbSNP","start":140553157,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140553157,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797208154"},{"seq_region_name":"7","id":"rs1229605444","clinical_significance":[],"alleles":["T","C"],"end":140553158,"strand":1,"feature_type":"variation","start":140553158,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1294259057","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140553160,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553160},{"id":"rs577327573","seq_region_name":"7","clinical_significance":[],"start":140553161,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140553161,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140553163,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553163,"source":"dbSNP","id":"rs1797208620","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs996625250","alleles":["C","T"],"end":140553167,"feature_type":"variation","strand":1,"source":"dbSNP","start":140553167,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1028459922","source":"dbSNP","start":140553168,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140553168,"feature_type":"variation","strand":1},{"id":"rs1585613179","seq_region_name":"7","clinical_significance":[],"end":140553190,"alleles":["GGGCGTTTCTCCGAGAGGGGG","GG"],"strand":1,"feature_type":"variation","start":140553170,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1797209076","seq_region_name":"7","clinical_significance":[],"start":140553171,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140553182,"alleles":["GGCGTTTCTCCG","G"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553173,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140553173,"clinical_significance":[],"seq_region_name":"7","id":"rs957923489"},{"id":"rs1797209282","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553174,"source":"dbSNP","strand":1,"feature_type":"variation","end":140553174,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1027111949","feature_type":"variation","strand":1,"end":140553178,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553178},{"source":"dbSNP","start":140553181,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140553181,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585613222"},{"source":"dbSNP","start":140553182,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140553182,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs886966379","seq_region_name":"7"},{"source":"dbSNP","start":140553184,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140553184,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797209763"},{"start":140553185,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140553185,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1373577576","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797209982","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553186,"feature_type":"variation","strand":1,"alleles":["GGGGG","GGGG"],"end":140553190},{"seq_region_name":"7","id":"rs1172712698","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553187,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140553187},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797210082","source":"dbSNP","start":140553188,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140553188,"alleles":["G","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1585613258","clinical_significance":[],"start":140553189,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140553189,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1277829832","seq_region_name":"7","alleles":["G","A"],"end":140553193,"feature_type":"variation","strand":1,"source":"dbSNP","start":140553193,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140553196,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140553196,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1346153970","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1004439166","feature_type":"variation","strand":1,"end":140553200,"alleles":["G","C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553200},{"clinical_significance":[],"seq_region_name":"7","id":"rs989313290","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140553201,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553201},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585613313","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553206,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140553206},{"clinical_significance":[],"id":"rs1797210911","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553211,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140553211},{"source":"dbSNP","start":140553213,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140553213,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs2130548851","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553214,"source":"dbSNP","strand":1,"feature_type":"variation","end":140553214,"alleles":["A","T"],"id":"rs1020920029","seq_region_name":"7","clinical_significance":[]},{"start":140553217,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140553217,"alleles":["G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797211118","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1019566219","end":140553219,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140553219,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs541406895","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553223,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140553223},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553224,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140553224,"seq_region_name":"7","id":"rs965285621","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553225,"feature_type":"variation","strand":1,"end":140553225,"alleles":["G","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1484937754"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553226,"feature_type":"variation","strand":1,"end":140553226,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1797211761"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553228,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140553228,"clinical_significance":[],"id":"rs966627374","seq_region_name":"7"},{"start":140553231,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140553231,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs1280275490","seq_region_name":"7","clinical_significance":[]},{"end":140553233,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140553233,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1797212082","seq_region_name":"7"},{"seq_region_name":"7","id":"rs541749775","clinical_significance":[],"alleles":["A","G"],"end":140553234,"strand":1,"feature_type":"variation","start":140553234,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140553235,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553235,"source":"dbSNP","seq_region_name":"7","id":"rs1344723779","clinical_significance":[]},{"end":140553237,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140553237,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1293924008","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797212374","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553240,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["ACGTGAAC","AC"],"end":140553247},{"seq_region_name":"7","id":"rs981988086","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553241,"source":"dbSNP","strand":1,"feature_type":"variation","end":140553241,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs928672248","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553242,"source":"dbSNP","strand":1,"feature_type":"variation","end":140553242,"alleles":["G","A"]},{"alleles":["G","T"],"end":140553244,"feature_type":"variation","strand":1,"source":"dbSNP","start":140553244,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1797212694","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140553247,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553247,"clinical_significance":[],"seq_region_name":"7","id":"rs1797212796"},{"feature_type":"variation","strand":1,"end":140553253,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553253,"clinical_significance":[],"seq_region_name":"7","id":"rs757595665"},{"seq_region_name":"7","id":"rs1028334314","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553262,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140553262},{"seq_region_name":"7","id":"rs938653153","clinical_significance":[],"end":140553264,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140553264,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553266,"source":"dbSNP","strand":1,"feature_type":"variation","end":140553266,"alleles":["G","A","C"],"seq_region_name":"7","id":"rs1797213195","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797213292","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553268,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140553268},{"seq_region_name":"7","id":"rs1449594373","clinical_significance":[],"start":140553274,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140553274,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553281,"source":"dbSNP","strand":1,"feature_type":"variation","end":140553281,"alleles":["A","T"],"seq_region_name":"7","id":"rs991617604","clinical_significance":[]},{"seq_region_name":"7","id":"rs1184809824","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553285,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140553285},{"clinical_significance":[],"seq_region_name":"7","id":"rs969082597","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553287,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140553287},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140553288,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553288,"clinical_significance":[],"id":"rs1430387571","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1797213911","clinical_significance":[],"end":140553289,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140553289,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140553298,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140553298,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585613523","clinical_significance":[]},{"source":"dbSNP","start":140553299,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140553299,"alleles":["A","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1372145166"},{"alleles":["A","G"],"end":140553301,"feature_type":"variation","strand":1,"source":"dbSNP","start":140553301,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1168139632"},{"id":"rs1797214544","seq_region_name":"7","clinical_significance":[],"end":140553302,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140553302,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["G","A"],"end":140553303,"feature_type":"variation","strand":1,"source":"dbSNP","start":140553303,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs915962627"},{"seq_region_name":"7","id":"rs1797214870","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140553304,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553304,"source":"dbSNP"},{"source":"dbSNP","start":140553306,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140553306,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs978885621","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553307,"source":"dbSNP","strand":1,"feature_type":"variation","end":140553307,"alleles":["A","G"],"seq_region_name":"7","id":"rs1797215232","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797215418","clinical_significance":[],"alleles":["C","T"],"end":140553310,"strand":1,"feature_type":"variation","start":140553310,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1414803428","clinical_significance":[],"start":140553311,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140553311,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1797215752","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553311,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["ATA","A"],"end":140553313},{"clinical_significance":[],"id":"rs1797215938","seq_region_name":"7","feature_type":"variation","strand":1,"end":140553312,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553312},{"seq_region_name":"7","id":"rs1797216109","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553313,"source":"dbSNP","strand":1,"feature_type":"variation","end":140553313,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1183632590","feature_type":"variation","strand":1,"end":140553325,"alleles":["AATG","AATGAATG"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553322},{"clinical_significance":[],"seq_region_name":"7","id":"rs552520563","feature_type":"variation","strand":1,"end":140553323,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553323},{"seq_region_name":"7","id":"rs1797216672","clinical_significance":[],"start":140553330,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140553330,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1797216854","seq_region_name":"7","end":140553332,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140553332,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140553332,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140553334,"alleles":["AAA","AAAA"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs35112090","clinical_significance":[]},{"seq_region_name":"7","id":"rs1261149441","clinical_significance":[],"alleles":["AGCAG","AG"],"end":140553338,"strand":1,"feature_type":"variation","start":140553334,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553335,"feature_type":"variation","strand":1,"end":140553335,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs142996758"},{"end":140553340,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140553340,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1048535531","clinical_significance":[]},{"seq_region_name":"7","id":"rs934876539","clinical_significance":[],"start":140553342,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140553342,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs751733673","clinical_significance":[],"end":140553344,"alleles":["GC","GCTGCCCGC"],"strand":1,"feature_type":"variation","start":140553343,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1797217857","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140553345,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553345,"source":"dbSNP"},{"seq_region_name":"7","id":"rs2130549261","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140553349,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553349,"source":"dbSNP"},{"alleles":["G","A"],"end":140553359,"feature_type":"variation","strand":1,"source":"dbSNP","start":140553359,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs887241790"},{"id":"rs1585613674","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140553361,"strand":1,"feature_type":"variation","start":140553361,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1393553009","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140553362,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553362},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797218262","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553364,"feature_type":"variation","strand":1,"alleles":["A","C","T"],"end":140553364},{"seq_region_name":"7","id":"rs531542448","clinical_significance":[],"start":140553365,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140553365,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1204289384","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140553367,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553367},{"seq_region_name":"7","id":"rs1041257081","clinical_significance":[],"end":140553368,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140553368,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553369,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140553369,"clinical_significance":[],"seq_region_name":"7","id":"rs900848192"},{"seq_region_name":"7","id":"rs1159054951","clinical_significance":[],"start":140553370,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140553370,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797219015","end":140553375,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140553375,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553379,"source":"dbSNP","strand":1,"feature_type":"variation","end":140553381,"alleles":["TAT","T"],"seq_region_name":"7","id":"rs1352998911","clinical_significance":[]},{"seq_region_name":"7","id":"rs1292178615","clinical_significance":[],"start":140553380,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140553380,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140553381,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553381,"clinical_significance":[],"seq_region_name":"7","id":"rs1797219317"},{"feature_type":"variation","strand":1,"alleles":["T","-"],"end":140553381,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553381,"clinical_significance":[],"id":"rs1797219432","seq_region_name":"7"},{"alleles":["T","C"],"end":140553387,"strand":1,"feature_type":"variation","start":140553387,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs917541525","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs996901245","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553392,"source":"dbSNP","strand":1,"feature_type":"variation","end":140553392,"alleles":["C","G","T"]},{"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140553393,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553393,"clinical_significance":[],"seq_region_name":"7","id":"rs1028094625"},{"seq_region_name":"7","id":"rs1362327232","clinical_significance":[],"start":140553396,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140553396,"alleles":["C","A","G","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs188938422","source":"dbSNP","start":140553397,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140553397,"alleles":["G","A","C"],"feature_type":"variation","strand":1},{"id":"rs1044591530","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140553400,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553400,"source":"dbSNP"},{"source":"dbSNP","start":140553401,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140553401,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797220311"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140553402,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553402,"clinical_significance":[],"seq_region_name":"7","id":"rs1451561486"},{"clinical_significance":[],"seq_region_name":"7","id":"rs181629804","alleles":["C","T"],"end":140553404,"feature_type":"variation","strand":1,"source":"dbSNP","start":140553404,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1010628086","end":140553405,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140553405,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553405,"feature_type":"variation","strand":1,"end":140553407,"alleles":["GGG","GG"],"clinical_significance":[],"id":"rs1563135763","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1797220910","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140553406,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553406,"source":"dbSNP"},{"seq_region_name":"7","id":"rs568143835","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140553407,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553407,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553408,"feature_type":"variation","strand":1,"alleles":["TTTT","TTT"],"end":140553411,"clinical_significance":[],"seq_region_name":"7","id":"rs1160067916"},{"seq_region_name":"7","id":"rs1797221265","clinical_significance":[],"alleles":["T","C"],"end":140553413,"strand":1,"feature_type":"variation","start":140553413,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797221347","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140553415,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553415},{"seq_region_name":"7","id":"rs1473827418","clinical_significance":[],"end":140553416,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140553416,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140553417,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140553417,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1020804123"},{"seq_region_name":"7","id":"rs1176948895","clinical_significance":[],"start":140553421,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140553421,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"start":140553425,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140553425,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1489026013","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553429,"feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140553429,"clinical_significance":[],"id":"rs1797221873","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1563135779","seq_region_name":"7","source":"dbSNP","start":140553431,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140553431,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs572086281","alleles":["G","A"],"end":140553432,"feature_type":"variation","strand":1,"source":"dbSNP","start":140553432,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140553437,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553437,"clinical_significance":[],"seq_region_name":"7","id":"rs1215146525"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553439,"source":"dbSNP","strand":1,"feature_type":"variation","end":140553439,"alleles":["C","T"],"seq_region_name":"7","id":"rs542677668","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","-"],"end":140553439,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553439,"clinical_significance":[],"seq_region_name":"7","id":"rs1797222424"},{"seq_region_name":"7","id":"rs184734845","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140553440,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553440,"source":"dbSNP"},{"start":140553443,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140553443,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1382650296","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs886839322","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553449,"feature_type":"variation","strand":1,"end":140553449,"alleles":["C","T"]},{"clinical_significance":[],"id":"rs1797222929","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140553450,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553450},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140553452,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553452,"source":"dbSNP","seq_region_name":"7","id":"rs1369839915","clinical_significance":[]},{"source":"dbSNP","start":140553453,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140553453,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1797223153","seq_region_name":"7"},{"end":140553456,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140553456,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs750876721","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1304811674","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140553457,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553457},{"id":"rs1223195113","seq_region_name":"7","clinical_significance":[],"start":140553460,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140553460,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797223679","source":"dbSNP","start":140553463,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140553463,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553463,"feature_type":"variation","strand":1,"alleles":["TT","-"],"end":140553464,"clinical_significance":[],"id":"rs1797223808","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1797223938","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553465,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140553465},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553467,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140553467,"clinical_significance":[],"seq_region_name":"7","id":"rs1797224059"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553468,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140553468,"seq_region_name":"7","id":"rs991896855","clinical_significance":[]},{"clinical_significance":[],"id":"rs1797224269","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553470,"feature_type":"variation","strand":1,"end":140553470,"alleles":["A","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553472,"feature_type":"variation","strand":1,"end":140553472,"alleles":["C","A"],"clinical_significance":[],"id":"rs1327745685","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs547542490","source":"dbSNP","start":140553473,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140553473,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs10952734","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","G","T"],"end":140553475,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553475,"source":"dbSNP"},{"clinical_significance":[],"id":"rs769181188","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553478,"feature_type":"variation","strand":1,"end":140553478,"alleles":["A","C"]},{"source":"dbSNP","start":140553479,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140553479,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797224925"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1321230055","feature_type":"variation","strand":1,"end":140553483,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553483},{"end":140553484,"alleles":["A","G","T"],"strand":1,"feature_type":"variation","start":140553484,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs539402033","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","G"],"end":140553486,"strand":1,"feature_type":"variation","start":140553486,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs931404653","clinical_significance":[]},{"clinical_significance":[],"id":"rs996767624","seq_region_name":"7","alleles":["C","T"],"end":140553487,"feature_type":"variation","strand":1,"source":"dbSNP","start":140553487,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1797225608","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553488,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140553488},{"clinical_significance":[],"id":"rs984129728","seq_region_name":"7","end":140553489,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140553489,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1797225850","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553497,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140553497},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553498,"source":"dbSNP","strand":1,"feature_type":"variation","end":140553498,"alleles":["T","C"],"seq_region_name":"7","id":"rs908732176","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs940162476","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553500,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140553500},{"seq_region_name":"7","id":"rs1214286090","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553501,"source":"dbSNP","strand":1,"feature_type":"variation","end":140553501,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs558040210","clinical_significance":[],"end":140553504,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140553504,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["C","G"],"end":140553506,"strand":1,"feature_type":"variation","start":140553506,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1260726373","clinical_significance":[]},{"clinical_significance":[],"id":"rs1192216240","seq_region_name":"7","source":"dbSNP","start":140553507,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140553507,"alleles":["T","C"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140553509,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140553509,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797226653"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1488833734","source":"dbSNP","start":140553510,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140553510,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1215676537","source":"dbSNP","start":140553511,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140553511,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1797227025","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553514,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140553514},{"feature_type":"variation","strand":1,"alleles":["C","A","G"],"end":140553516,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553516,"clinical_significance":[],"id":"rs1251326022","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553520,"source":"dbSNP","strand":1,"feature_type":"variation","end":140553520,"alleles":["C","A"],"seq_region_name":"7","id":"rs1041325881","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","A","G"],"end":140553521,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553521,"source":"dbSNP","seq_region_name":"7","id":"rs1797227377","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140553522,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553522,"source":"dbSNP","seq_region_name":"7","id":"rs1028218359","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797227654","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553523,"feature_type":"variation","strand":1,"end":140553523,"alleles":["T","A"]},{"id":"rs1208752800","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553527,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["-","C"],"end":140553526},{"clinical_significance":[],"seq_region_name":"7","id":"rs1321117089","end":140553527,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140553527,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140553528,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["GGGTGTCGGG","GGG"],"end":140553537,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797228016"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1258474001","source":"dbSNP","start":140553529,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140553529,"alleles":["G","A"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553534,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140553534,"seq_region_name":"7","id":"rs1238233961","clinical_significance":[]},{"start":140553535,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140553535,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs189649119","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553537,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140553537,"id":"rs1305279863","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797228659","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553538,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140553538},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140553540,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553540,"source":"dbSNP","seq_region_name":"7","id":"rs1797228764","clinical_significance":[]},{"end":140553541,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140553541,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs932371287","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140553544,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553544,"clinical_significance":[],"seq_region_name":"7","id":"rs1797229008"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1000593552","source":"dbSNP","start":140553546,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140553546,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1178957447","seq_region_name":"7","source":"dbSNP","start":140553547,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140553547,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140553548,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553548,"source":"dbSNP","id":"rs1031781102","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","T"],"end":140553553,"feature_type":"variation","strand":1,"source":"dbSNP","start":140553553,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797229494"},{"clinical_significance":[],"id":"rs956318655","seq_region_name":"7","feature_type":"variation","strand":1,"end":140553554,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553554},{"seq_region_name":"7","id":"rs537341597","clinical_significance":[],"strand":1,"feature_type":"variation","end":140553561,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553561,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797229868","source":"dbSNP","start":140553564,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140553564,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1382843812","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140553565,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553565,"source":"dbSNP"},{"end":140553568,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140553568,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs555954385","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140553575,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553575,"clinical_significance":[],"seq_region_name":"7","id":"rs1158269127"},{"id":"rs1377813904","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553576,"source":"dbSNP","strand":1,"feature_type":"variation","end":140553576,"alleles":["T","C"]},{"clinical_significance":[],"id":"rs1350451466","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140553581,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553581},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140553584,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553584,"source":"dbSNP","seq_region_name":"7","id":"rs1010680343","clinical_significance":[]},{"end":140553589,"alleles":["CTATC","CTATCTATC"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140553585,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1563135944","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1188768137","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553586,"feature_type":"variation","strand":1,"end":140553586,"alleles":["T","A"]},{"end":140553586,"alleles":["T","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140553586,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1391218612"},{"clinical_significance":[],"id":"rs1797231004","seq_region_name":"7","alleles":["A","G"],"end":140553587,"feature_type":"variation","strand":1,"source":"dbSNP","start":140553587,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140553588,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553588,"clinical_significance":[],"seq_region_name":"7","id":"rs1458968427"},{"source":"dbSNP","start":140553590,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140553590,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1259038389"},{"clinical_significance":[],"id":"rs1204046695","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553592,"feature_type":"variation","strand":1,"end":140553592,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs531349745","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553595,"feature_type":"variation","strand":1,"end":140553595,"alleles":["A","G"]},{"clinical_significance":[],"id":"rs1282428374","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140553597,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553597},{"id":"rs1797231711","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140553599,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553599,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs543497886","feature_type":"variation","strand":1,"end":140553603,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553603},{"clinical_significance":[],"id":"rs1797231932","seq_region_name":"7","source":"dbSNP","start":140553604,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140553604,"alleles":["C","T"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140553605,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553605,"source":"dbSNP","seq_region_name":"7","id":"rs1003360112","clinical_significance":[]},{"source":"dbSNP","start":140553609,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140553609,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1346856059"},{"source":"dbSNP","start":140553610,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140553610,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs779525648","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1229882589","clinical_significance":[],"strand":1,"feature_type":"variation","end":140553612,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553612,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1324965464","clinical_significance":[],"start":140553616,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140553616,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"start":140553618,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140553618,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1310369938","clinical_significance":[]},{"id":"rs749006483","seq_region_name":"7","clinical_significance":[],"end":140553620,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140553620,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130550328","feature_type":"variation","strand":1,"end":140553624,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553624},{"id":"rs908321358","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140553625,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553625,"source":"dbSNP"},{"start":140553626,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140553626,"alleles":["T","G"],"strand":1,"feature_type":"variation","id":"rs1797232909","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553627,"source":"dbSNP","strand":1,"feature_type":"variation","end":140553627,"alleles":["A","G"],"seq_region_name":"7","id":"rs1797233023","clinical_significance":[]},{"alleles":["G","A"],"end":140553629,"strand":1,"feature_type":"variation","start":140553629,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs879186198","clinical_significance":[]},{"seq_region_name":"7","id":"rs139491768","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553632,"source":"dbSNP","strand":1,"feature_type":"variation","end":140553632,"alleles":["G","C"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553635,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140553635,"clinical_significance":[],"seq_region_name":"7","id":"rs1797233385"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1023389294","source":"dbSNP","start":140553636,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140553636,"alleles":["T","A","C"],"feature_type":"variation","strand":1},{"id":"rs180833715","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140553637,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553637,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1797233825","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553639,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140553639},{"clinical_significance":[],"seq_region_name":"7","id":"rs1040775679","feature_type":"variation","strand":1,"end":140553645,"alleles":["GCGGC","GCGGCGGC"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553641},{"clinical_significance":[],"id":"rs4289723","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553642,"feature_type":"variation","strand":1,"alleles":["C","A","G","T"],"end":140553642},{"end":140553643,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140553643,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1475264018","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553645,"feature_type":"variation","strand":1,"end":140553645,"alleles":["C","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1259067101"},{"seq_region_name":"7","id":"rs1185674307","clinical_significance":[],"strand":1,"feature_type":"variation","end":140553646,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553646,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553648,"feature_type":"variation","strand":1,"end":140553648,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs572071507"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553650,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140553650,"clinical_significance":[],"seq_region_name":"7","id":"rs908618543"},{"seq_region_name":"7","id":"rs1468151761","clinical_significance":[],"strand":1,"feature_type":"variation","end":140553651,"alleles":["G","A","C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553651,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553652,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140553652,"clinical_significance":[],"id":"rs1245864545","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1336998493","clinical_significance":[],"end":140553654,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140553654,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1291586512","clinical_significance":[],"strand":1,"feature_type":"variation","end":140553656,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553656,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1199500636","clinical_significance":[],"start":140553658,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140553658,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140553660,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553660,"clinical_significance":[],"seq_region_name":"7","id":"rs1797236305"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797236426","source":"dbSNP","start":140553661,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140553661,"alleles":["T","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs961545935","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140553664,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553664},{"id":"rs1797236676","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553665,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140553665},{"clinical_significance":[],"id":"rs1331213014","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140553667,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553667},{"strand":1,"feature_type":"variation","alleles":["T","TT"],"end":140553667,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553667,"source":"dbSNP","id":"rs1797236905","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","-"],"end":140553671,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553671,"source":"dbSNP","seq_region_name":"7","id":"rs1797237013","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs977320211","alleles":["C","T"],"end":140553673,"feature_type":"variation","strand":1,"source":"dbSNP","start":140553673,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140553676,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553676,"clinical_significance":[],"seq_region_name":"7","id":"rs1797237251"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553678,"source":"dbSNP","strand":1,"feature_type":"variation","end":140553678,"alleles":["G","C"],"seq_region_name":"7","id":"rs1797237364","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553680,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140553680,"seq_region_name":"7","id":"rs1393813834","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797237587","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["TTAGG","TTAGGTTAGG"],"end":140553684,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553680,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797237714","feature_type":"variation","strand":1,"end":140553684,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553684},{"clinical_significance":[],"seq_region_name":"7","id":"rs545773168","source":"dbSNP","start":140553687,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140553687,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs904421301","seq_region_name":"7","end":140553691,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140553691,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1797238073","seq_region_name":"7","source":"dbSNP","start":140553692,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140553692,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs932901303","clinical_significance":[],"end":140553694,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140553694,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["CTCT","CT"],"end":140553700,"feature_type":"variation","strand":1,"source":"dbSNP","start":140553697,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs764210838"},{"seq_region_name":"7","id":"rs1162244541","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["CTTAACGAGCATGCTGC","C"],"end":140553715,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553699,"source":"dbSNP"},{"source":"dbSNP","start":140553701,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140553710,"alleles":["TAACGAGCAT","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1797238527","seq_region_name":"7"},{"source":"dbSNP","start":140553704,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140553704,"alleles":["C","A","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs74700036"},{"seq_region_name":"7","id":"rs914925644","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553705,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140553705},{"seq_region_name":"7","id":"rs1435843616","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553708,"source":"dbSNP","strand":1,"feature_type":"variation","end":140553708,"alleles":["C","A","T"]},{"seq_region_name":"7","id":"rs1176448057","clinical_significance":[],"start":140553709,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140553709,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553710,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","G"],"end":140553710,"id":"rs531667442","seq_region_name":"7","clinical_significance":[]},{"id":"rs1414390653","seq_region_name":"7","clinical_significance":[],"start":140553715,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140553715,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"id":"rs1470036436","seq_region_name":"7","clinical_significance":[],"end":140553719,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140553719,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553722,"feature_type":"variation","strand":1,"end":140553722,"alleles":["G","-"],"clinical_significance":[],"id":"rs1271285122","seq_region_name":"7"},{"id":"rs946353299","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553724,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140553724},{"seq_region_name":"7","id":"rs1281806442","clinical_significance":[],"start":140553725,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140553727,"alleles":["TCT","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1476159989","seq_region_name":"7","source":"dbSNP","start":140553726,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140553726,"alleles":["C","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1335519464","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140553734,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553734,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1324703192","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553735,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140553735},{"end":140553751,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140553751,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1441166707"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1396240733","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553752,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140553752},{"seq_region_name":"7","id":"rs1797240599","clinical_significance":[],"start":140553753,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140553753,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140553754,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553754,"source":"dbSNP","seq_region_name":"7","id":"rs1323231287","clinical_significance":[]},{"seq_region_name":"7","id":"rs549795032","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553761,"source":"dbSNP","strand":1,"feature_type":"variation","end":140553761,"alleles":["C","G"]},{"seq_region_name":"7","id":"rs1797240938","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140553763,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553763,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1460495519","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553766,"feature_type":"variation","strand":1,"end":140553766,"alleles":["T","C"]},{"strand":1,"feature_type":"variation","end":140553769,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553769,"source":"dbSNP","seq_region_name":"7","id":"rs1162105627","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140553770,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553770,"source":"dbSNP","id":"rs1797241367","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140553774,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140553774,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797241474"},{"source":"dbSNP","start":140553775,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140553775,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs956034005","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1014297235","feature_type":"variation","strand":1,"alleles":["GG","G"],"end":140553778,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553777},{"start":140553781,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140553781,"strand":1,"feature_type":"variation","id":"rs1024321803","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs189489718","end":140553782,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140553782,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs547312678","source":"dbSNP","start":140553783,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140553783,"alleles":["A","G","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1213092369","clinical_significance":[],"end":140553787,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140553787,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140553788,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["-","AT"],"end":140553787,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs569043883"},{"source":"dbSNP","start":140553788,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140553788,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1563136127"},{"seq_region_name":"7","id":"rs1003412029","clinical_significance":[],"strand":1,"feature_type":"variation","end":140553790,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553790,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553792,"feature_type":"variation","strand":1,"end":140553792,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1447636322"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585615115","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140553794,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553794},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553799,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140553799,"id":"rs1797243220","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1797243324","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553800,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140553800},{"end":140553801,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140553801,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs920893411","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1056709061","clinical_significance":[],"start":140553802,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140553802,"alleles":["G","A","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797243684","end":140553803,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140553803,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","G","T"],"end":140553804,"strand":1,"feature_type":"variation","start":140553804,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs529052965","clinical_significance":[]},{"id":"rs181141604","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140553805,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553805,"source":"dbSNP"},{"seq_region_name":"7","id":"rs565797067","clinical_significance":[],"start":140553806,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140553806,"strand":1,"feature_type":"variation"},{"start":140553809,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C"],"end":140553809,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs185495822","clinical_significance":[]},{"seq_region_name":"7","id":"rs1345265703","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553812,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140553812},{"feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140553813,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553813,"clinical_significance":[],"seq_region_name":"7","id":"rs1319784154"},{"seq_region_name":"7","id":"rs1797244520","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553816,"source":"dbSNP","strand":1,"feature_type":"variation","end":140553816,"alleles":["G","A"]},{"end":140553819,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140553819,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs565604972"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553820,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140553820,"seq_region_name":"7","id":"rs1585615221","clinical_significance":[]},{"end":140553821,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140553821,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1173986584"},{"clinical_significance":[],"seq_region_name":"7","id":"rs771857048","source":"dbSNP","start":140553825,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TT","TTT"],"end":140553826,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1455436770","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553826,"feature_type":"variation","strand":1,"end":140553826,"alleles":["T","C"]},{"clinical_significance":[],"id":"rs1797245259","seq_region_name":"7","source":"dbSNP","start":140553830,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140553830,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1219377678","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140553831,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553831},{"clinical_significance":[],"id":"rs1275344316","seq_region_name":"7","feature_type":"variation","strand":1,"end":140553832,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553832},{"clinical_significance":[],"id":"rs1797245612","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553833,"feature_type":"variation","strand":1,"end":140553833,"alleles":["A","C"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553834,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140553834,"clinical_significance":[],"seq_region_name":"7","id":"rs952741521"},{"end":140553835,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140553835,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs932497894"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553836,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140553836,"clinical_significance":[],"id":"rs1005487872","seq_region_name":"7"},{"end":140553839,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140553839,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1237855073","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1191133877","seq_region_name":"7","end":140553848,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140553848,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["A","T"],"end":140553849,"strand":1,"feature_type":"variation","start":140553849,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs904474744","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553855,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140553855,"seq_region_name":"7","id":"rs1797246353","clinical_significance":[]},{"id":"rs1797246453","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140553857,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553857,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1281709182","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553859,"feature_type":"variation","strand":1,"end":140553880,"alleles":["GTACAGAACAAAATGGAGTCTC","-"]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140553860,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553860,"clinical_significance":[],"seq_region_name":"7","id":"rs1797246647"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797246738","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553863,"feature_type":"variation","strand":1,"end":140553863,"alleles":["A","G"]},{"source":"dbSNP","start":140553867,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140553867,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797246916"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1213407056","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553868,"feature_type":"variation","strand":1,"end":140553871,"alleles":["AAAA","AAA"]},{"seq_region_name":"7","id":"rs113829050","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553869,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140553869},{"id":"rs1000529625","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140553871,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553871,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553876,"source":"dbSNP","strand":1,"feature_type":"variation","end":140553876,"alleles":["G","A","C"],"seq_region_name":"7","id":"rs1015668360","clinical_significance":[]},{"id":"rs1797247835","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553880,"source":"dbSNP","strand":1,"feature_type":"variation","end":140553880,"alleles":["C","G","T"]},{"id":"rs1797248016","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553881,"source":"dbSNP","strand":1,"feature_type":"variation","end":140553881,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1053004523","feature_type":"variation","strand":1,"end":140553882,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553882},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140553884,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553884,"clinical_significance":[],"id":"rs1797248380","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1486575418","end":140553886,"alleles":["T","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140553886,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140553889,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553889,"clinical_significance":[],"seq_region_name":"7","id":"rs1585615411"},{"strand":1,"feature_type":"variation","alleles":["CTTCTT","CTT"],"end":140553895,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553890,"source":"dbSNP","seq_region_name":"7","id":"rs1585615422","clinical_significance":[]},{"seq_region_name":"7","id":"rs1233092741","clinical_significance":[],"alleles":["T","C"],"end":140553891,"strand":1,"feature_type":"variation","start":140553891,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["T","A"],"end":140553892,"strand":1,"feature_type":"variation","start":140553892,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1362241190","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553898,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140553898,"clinical_significance":[],"seq_region_name":"7","id":"rs1185708869"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553899,"feature_type":"variation","strand":1,"end":140553899,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1797249387"},{"id":"rs2130551374","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553899,"source":"dbSNP","strand":1,"feature_type":"variation","end":140553903,"alleles":["ACACA","ACA"]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140553902,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553902,"clinical_significance":[],"seq_region_name":"7","id":"rs1271358823"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1428071373","end":140553906,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140553906,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1256796137","clinical_significance":[],"strand":1,"feature_type":"variation","end":140553908,"alleles":["C","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553908,"source":"dbSNP"},{"id":"rs368191583","seq_region_name":"7","clinical_significance":[],"start":140553909,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140553909,"alleles":["A","-"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797249813","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553909,"feature_type":"variation","strand":1,"end":140553909,"alleles":["A","T"]},{"seq_region_name":"7","id":"rs961451886","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553911,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140553911},{"alleles":["AA","AAA"],"end":140553913,"feature_type":"variation","strand":1,"source":"dbSNP","start":140553912,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797250150"},{"seq_region_name":"7","id":"rs976826132","clinical_significance":[],"start":140553916,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140553916,"strand":1,"feature_type":"variation"},{"alleles":["TCTCTCT","TCTCT"],"end":140553928,"strand":1,"feature_type":"variation","start":140553922,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797250351","clinical_significance":[]},{"seq_region_name":"7","id":"rs1373392754","clinical_significance":[],"start":140553925,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G","T"],"end":140553925,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140553926,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553926,"clinical_significance":[],"seq_region_name":"7","id":"rs1797250582"},{"strand":1,"feature_type":"variation","end":140553934,"alleles":["TCTTTCTTT","TCTTT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553926,"source":"dbSNP","seq_region_name":"7","id":"rs1172851012","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140553930,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553930,"clinical_significance":[],"seq_region_name":"7","id":"rs2130551471"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553934,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140553934,"clinical_significance":[],"seq_region_name":"7","id":"rs1797250776"},{"end":140553935,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140553935,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1014182580"},{"feature_type":"variation","strand":1,"end":140553936,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553936,"clinical_significance":[],"seq_region_name":"7","id":"rs1409022045"},{"seq_region_name":"7","id":"rs1797251098","clinical_significance":[],"start":140553936,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["CCCC","CCCCC"],"end":140553939,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140553938,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553938,"source":"dbSNP","id":"rs1797251202","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1421922839","source":"dbSNP","start":140553943,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140553943,"feature_type":"variation","strand":1},{"end":140553945,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140553945,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs922781085"},{"end":140553946,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140553946,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs529923848"},{"source":"dbSNP","start":140553948,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140553948,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585615635"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553949,"feature_type":"variation","strand":1,"end":140553949,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs551409776"},{"end":140553950,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140553950,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs569693241"},{"end":140553951,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140553951,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1190687000","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797251820","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553955,"feature_type":"variation","strand":1,"end":140553955,"alleles":["C","A"]},{"clinical_significance":[],"id":"rs1001690108","seq_region_name":"7","alleles":["G","A","T"],"end":140553957,"feature_type":"variation","strand":1,"source":"dbSNP","start":140553957,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140553961,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140553961,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797252090","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553962,"feature_type":"variation","strand":1,"end":140553962,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1437033960"},{"end":140553963,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140553963,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797252286","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553964,"feature_type":"variation","strand":1,"end":140553964,"alleles":["G","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1017612466"},{"source":"dbSNP","start":140553965,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C","G"],"end":140553965,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797252509"},{"id":"rs1307674157","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140553966,"strand":1,"feature_type":"variation","start":140553966,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["T","C"],"end":140553971,"feature_type":"variation","strand":1,"source":"dbSNP","start":140553971,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797252724"},{"source":"dbSNP","start":140553973,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140553973,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1797252834","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140553975,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553975,"clinical_significance":[],"id":"rs1028243951","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1797253040","seq_region_name":"7","alleles":["C","T"],"end":140553977,"feature_type":"variation","strand":1,"source":"dbSNP","start":140553977,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1311569500","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553977,"source":"dbSNP","strand":1,"feature_type":"variation","end":140553992,"alleles":["CAGCACTTAGGGAGGC","C"]},{"seq_region_name":"7","id":"rs1797253270","clinical_significance":[],"start":140553979,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140553979,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553982,"source":"dbSNP","strand":1,"feature_type":"variation","end":140553982,"alleles":["C","T"],"id":"rs537782595","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140553985,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553985,"source":"dbSNP","seq_region_name":"7","id":"rs1293448995","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553986,"source":"dbSNP","strand":1,"feature_type":"variation","end":140553986,"alleles":["G","A"],"seq_region_name":"7","id":"rs915478801","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1416534606","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140553991,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553991},{"feature_type":"variation","strand":1,"end":140553993,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140553993,"clinical_significance":[],"seq_region_name":"7","id":"rs201679863"},{"end":140553994,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140553994,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs113251445","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs574198257","clinical_significance":[],"strand":1,"feature_type":"variation","end":140553996,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140553996,"source":"dbSNP"},{"alleles":["T","C","G"],"end":140553998,"feature_type":"variation","strand":1,"source":"dbSNP","start":140553998,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs958239498","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554001,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140554001,"seq_region_name":"7","id":"rs1797254367","clinical_significance":[]},{"seq_region_name":"7","id":"rs548321147","clinical_significance":[],"start":140554002,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140554002,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1409674061","seq_region_name":"7","source":"dbSNP","start":140554003,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140554003,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140554005,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554005,"source":"dbSNP","seq_region_name":"7","id":"rs1797254823","clinical_significance":[]},{"end":140554007,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140554007,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs570029768"},{"start":140554008,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140554008,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797255194","clinical_significance":[]},{"source":"dbSNP","start":140554009,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140554009,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs976398366"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1417810054","alleles":["G","A"],"end":140554010,"feature_type":"variation","strand":1,"source":"dbSNP","start":140554010,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1178085462","clinical_significance":[],"alleles":["A","-"],"end":140554011,"strand":1,"feature_type":"variation","start":140554011,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1056192360","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554012,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140554012},{"clinical_significance":[],"id":"rs1797255906","seq_region_name":"7","feature_type":"variation","strand":1,"end":140554017,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554017},{"feature_type":"variation","strand":1,"end":140554020,"alleles":["G","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554020,"clinical_significance":[],"seq_region_name":"7","id":"rs1585615929"},{"seq_region_name":"7","id":"rs142067729","clinical_significance":[],"end":140554021,"alleles":["A","G","T"],"strand":1,"feature_type":"variation","start":140554021,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1231565582","clinical_significance":[],"end":140554022,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140554022,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["C","G"],"end":140554023,"feature_type":"variation","strand":1,"source":"dbSNP","start":140554023,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1349770769"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1208528547","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554024,"feature_type":"variation","strand":1,"end":140554024,"alleles":["A","G"]},{"id":"rs1279467401","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140554028,"strand":1,"feature_type":"variation","start":140554028,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554029,"feature_type":"variation","strand":1,"end":140554029,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1273210019"},{"clinical_significance":[],"seq_region_name":"7","id":"rs150129226","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554031,"feature_type":"variation","strand":1,"alleles":["T","A","G"],"end":140554031},{"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140554034,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554034,"clinical_significance":[],"seq_region_name":"7","id":"rs1585616020"},{"seq_region_name":"7","id":"rs1332540354","clinical_significance":[],"alleles":["C","G","T"],"end":140554037,"strand":1,"feature_type":"variation","start":140554037,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140554038,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140554038,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1194622291","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140554041,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140554041,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1239863430"},{"clinical_significance":[],"id":"rs985194144","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554043,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140554043},{"seq_region_name":"7","id":"rs1191396887","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554044,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140554044},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797258405","source":"dbSNP","start":140554049,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140554048,"alleles":["-","T"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554051,"source":"dbSNP","strand":1,"feature_type":"variation","end":140554051,"alleles":["C","T"],"seq_region_name":"7","id":"rs1395497331","clinical_significance":[]},{"id":"rs1797258644","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554052,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140554052},{"seq_region_name":"7","id":"rs1048988897","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","G","T"],"end":140554054,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554054,"source":"dbSNP"},{"source":"dbSNP","start":140554055,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140554055,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1393894275"},{"clinical_significance":[],"id":"rs925784139","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140554059,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554059},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797259156","alleles":["T","C"],"end":140554060,"feature_type":"variation","strand":1,"source":"dbSNP","start":140554060,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1797259273","seq_region_name":"7","end":140554063,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140554063,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1797259373","clinical_significance":[],"start":140554068,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140554068,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1421469071","feature_type":"variation","strand":1,"alleles":["AAAAA","AAAA"],"end":140554076,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554072},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140554075,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554075,"clinical_significance":[],"seq_region_name":"7","id":"rs1797259578"},{"feature_type":"variation","strand":1,"end":140554077,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554077,"clinical_significance":[],"seq_region_name":"7","id":"rs1436935599"},{"feature_type":"variation","strand":1,"end":140554078,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554078,"clinical_significance":[],"seq_region_name":"7","id":"rs2130552126"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1172199839","alleles":["C","T"],"end":140554082,"feature_type":"variation","strand":1,"source":"dbSNP","start":140554082,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["G","A","C","T"],"end":140554083,"feature_type":"variation","strand":1,"source":"dbSNP","start":140554083,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1375322520"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554083,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GGG","GG"],"end":140554085,"id":"rs1438626943","seq_region_name":"7","clinical_significance":[]},{"end":140554085,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140554085,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1401811519","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1320296715","clinical_significance":[],"strand":1,"feature_type":"variation","end":140554086,"alleles":["T","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554086,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140554087,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554087,"source":"dbSNP","id":"rs1343507207","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797260520","end":140554092,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140554092,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1156518321","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554094,"feature_type":"variation","strand":1,"end":140554094,"alleles":["C","G","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554094,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CAT","-"],"end":140554096,"seq_region_name":"7","id":"rs746881690","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs935827383","source":"dbSNP","start":140554095,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140554095,"alleles":["A","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1373522094","feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140554096,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554096},{"seq_region_name":"7","id":"rs1231737686","clinical_significance":[],"start":140554097,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140554097,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1454177692","clinical_significance":[],"start":140554097,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140554097,"alleles":["G","GGG"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1302424667","alleles":["T","C"],"end":140554098,"feature_type":"variation","strand":1,"source":"dbSNP","start":140554098,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797261500","end":140554101,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140554101,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1439030332","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554103,"source":"dbSNP","strand":1,"feature_type":"variation","end":140554103,"alleles":["G","A"]},{"id":"rs1354242532","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140554106,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554106,"source":"dbSNP"},{"end":140554110,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140554110,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1797261839","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140554114,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554114,"clinical_significance":[],"seq_region_name":"7","id":"rs1797261951"},{"source":"dbSNP","start":140554115,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140554115,"alleles":["A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797262083"},{"strand":1,"feature_type":"variation","end":140554122,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554122,"source":"dbSNP","id":"rs1206816000","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1797262294","seq_region_name":"7","source":"dbSNP","start":140554126,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140554126,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140554129,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554129,"clinical_significance":[],"seq_region_name":"7","id":"rs1797262391"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797262575","source":"dbSNP","start":140554134,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140554134,"alleles":["G","A"],"feature_type":"variation","strand":1},{"start":140554139,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140554139,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797262722","clinical_significance":[]},{"seq_region_name":"7","id":"rs1445896606","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554140,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140554140},{"clinical_significance":[],"id":"rs1797263093","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554143,"feature_type":"variation","strand":1,"end":140554143,"alleles":["T","C"]},{"id":"rs1221710443","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554147,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140554147},{"seq_region_name":"7","id":"rs1455755589","clinical_significance":[],"alleles":["C","T"],"end":140554150,"strand":1,"feature_type":"variation","start":140554150,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1290524886","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554151,"feature_type":"variation","strand":1,"end":140554151,"alleles":["A","G"]},{"id":"rs1797263825","seq_region_name":"7","clinical_significance":[],"start":140554155,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140554155,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1158791221","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554158,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140554158},{"clinical_significance":[],"seq_region_name":"7","id":"rs1435753849","source":"dbSNP","start":140554159,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140554159,"alleles":["G","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797264302","alleles":["G","A"],"end":140554162,"feature_type":"variation","strand":1,"source":"dbSNP","start":140554162,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1397326596","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554163,"feature_type":"variation","strand":1,"end":140554163,"alleles":["T","C","G"]},{"end":140554172,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140554172,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585616419","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs190304390","alleles":["C","A"],"end":140554173,"feature_type":"variation","strand":1,"source":"dbSNP","start":140554173,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1452261406","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554174,"feature_type":"variation","strand":1,"end":140554174,"alleles":["C","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554175,"source":"dbSNP","strand":1,"feature_type":"variation","end":140554175,"alleles":["G","A"],"seq_region_name":"7","id":"rs887690493","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554178,"source":"dbSNP","strand":1,"feature_type":"variation","end":140554178,"alleles":["G","A","C"],"seq_region_name":"7","id":"rs1797265416","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140554180,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554180,"clinical_significance":[],"seq_region_name":"7","id":"rs1265983813"},{"start":140554181,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140554181,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1053461265","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140554182,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554182,"clinical_significance":[],"seq_region_name":"7","id":"rs1486783849"},{"feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140554183,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554183,"clinical_significance":[],"seq_region_name":"7","id":"rs1585616485"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797265887","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140554184,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554184},{"id":"rs1258909647","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140554185,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554185,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1254448945","source":"dbSNP","start":140554186,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140554186,"alleles":["C","A"],"feature_type":"variation","strand":1},{"id":"rs1452210637","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554187,"source":"dbSNP","strand":1,"feature_type":"variation","end":140554187,"alleles":["T","C"]},{"source":"dbSNP","start":140554188,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140554188,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797266317"},{"source":"dbSNP","start":140554189,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140554189,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130552536"},{"clinical_significance":[],"id":"rs1797266413","seq_region_name":"7","source":"dbSNP","start":140554190,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140554190,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1585616531","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140554191,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554191,"source":"dbSNP"},{"start":140554194,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140554194,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs891702419","clinical_significance":[]},{"start":140554197,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140554197,"alleles":["G","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797266817","clinical_significance":[]},{"start":140554198,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140554198,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797266909","clinical_significance":[]},{"start":140554199,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140554199,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1394863289","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585616568","feature_type":"variation","strand":1,"end":140554201,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554201},{"seq_region_name":"7","id":"rs757210477","clinical_significance":[],"strand":1,"feature_type":"variation","end":140554202,"alleles":["GG","GGG"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554201,"source":"dbSNP"},{"id":"rs183049955","seq_region_name":"7","clinical_significance":[],"start":140554203,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140554203,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs145585544","clinical_significance":[],"alleles":["G","A","T"],"end":140554204,"strand":1,"feature_type":"variation","start":140554204,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1797267467","clinical_significance":[],"strand":1,"feature_type":"variation","end":140554205,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554205,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1797267553","seq_region_name":"7","source":"dbSNP","start":140554206,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140554206,"alleles":["C","A"],"feature_type":"variation","strand":1},{"start":140554211,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140554211,"alleles":["C","A","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs558962150","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140554212,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554212,"clinical_significance":[],"seq_region_name":"7","id":"rs1797267829"},{"seq_region_name":"7","id":"rs1797267933","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140554214,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554214,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554215,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140554215,"clinical_significance":[],"seq_region_name":"7","id":"rs1585616633"},{"strand":1,"feature_type":"variation","end":140554219,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554219,"source":"dbSNP","seq_region_name":"7","id":"rs1326685557","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1415984307","feature_type":"variation","strand":1,"end":140554220,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554220},{"id":"rs561789349","seq_region_name":"7","clinical_significance":[],"alleles":["T","G"],"end":140554223,"strand":1,"feature_type":"variation","start":140554223,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1172176902","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554224,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140554224},{"strand":1,"feature_type":"variation","end":140554236,"alleles":["AAAAAAAAAAAA","AAAAAAAAAA","AAAAAAAAAAA","AAAAAAAAAAAAA","AAAAAAAAAAAAAA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554225,"source":"dbSNP","id":"rs879656542","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554226,"source":"dbSNP","strand":1,"feature_type":"variation","end":140554226,"alleles":["A","G"],"seq_region_name":"7","id":"rs1797268817","clinical_significance":[]},{"source":"dbSNP","start":140554230,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140554230,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs529095707"},{"id":"rs1797269039","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140554233,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554233,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554235,"feature_type":"variation","strand":1,"end":140554234,"alleles":["-","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1797269149"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554236,"source":"dbSNP","strand":1,"feature_type":"variation","end":140554235,"alleles":["-","C"],"seq_region_name":"7","id":"rs2130552750","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554237,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140554237,"clinical_significance":[],"seq_region_name":"7","id":"rs1797269251"},{"seq_region_name":"7","id":"rs1797269349","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554243,"source":"dbSNP","strand":1,"feature_type":"variation","end":140554243,"alleles":["T","C"]},{"end":140554246,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140554246,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1325556216"},{"seq_region_name":"7","id":"rs1797269592","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554248,"source":"dbSNP","strand":1,"feature_type":"variation","end":140554248,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130552794","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554249,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140554249},{"clinical_significance":[],"seq_region_name":"7","id":"rs1027715969","source":"dbSNP","start":140554253,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140554253,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs186219167","clinical_significance":[],"start":140554255,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140554255,"alleles":["C","A","T"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140554264,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554264,"source":"dbSNP","seq_region_name":"7","id":"rs2130552828","clinical_significance":[]},{"seq_region_name":"7","id":"rs1015552566","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554265,"source":"dbSNP","strand":1,"feature_type":"variation","end":140554265,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1344537172","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140554267,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554267,"source":"dbSNP"},{"seq_region_name":"7","id":"rs887956203","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554269,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140554269},{"source":"dbSNP","start":140554271,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140554271,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs192436767"},{"clinical_significance":[],"seq_region_name":"7","id":"rs182475763","feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140554272,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554272},{"clinical_significance":[],"seq_region_name":"7","id":"rs966282473","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140554273,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554273},{"id":"rs1797270645","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140554278,"strand":1,"feature_type":"variation","start":140554278,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554279,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140554279,"clinical_significance":[],"id":"rs1797270756","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140554280,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554280,"clinical_significance":[],"seq_region_name":"7","id":"rs1797270841"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554282,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140554282,"clinical_significance":[],"seq_region_name":"7","id":"rs1797270926"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1029735368","end":140554283,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140554283,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554285,"source":"dbSNP","strand":1,"feature_type":"variation","end":140554285,"alleles":["A","G"],"seq_region_name":"7","id":"rs1228347346","clinical_significance":[]},{"clinical_significance":[],"id":"rs1797271233","seq_region_name":"7","feature_type":"variation","strand":1,"end":140554289,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554289},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554291,"source":"dbSNP","strand":1,"feature_type":"variation","end":140554291,"alleles":["A","G"],"seq_region_name":"7","id":"rs533278692","clinical_significance":[]},{"seq_region_name":"7","id":"rs6964971","clinical_significance":[],"start":140554292,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140554292,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140554297,"alleles":["CCCC","CCCCC"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554294,"source":"dbSNP","id":"rs1797271546","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","G"],"end":140554299,"feature_type":"variation","strand":1,"source":"dbSNP","start":140554299,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1395831501"},{"seq_region_name":"7","id":"rs2130552966","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554301,"source":"dbSNP","strand":1,"feature_type":"variation","end":140554301,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs1466811950","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554302,"source":"dbSNP","strand":1,"feature_type":"variation","end":140554302,"alleles":["G","C"]},{"seq_region_name":"7","id":"rs1797271861","clinical_significance":[],"start":140554310,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AGA","A"],"end":140554312,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1797271956","clinical_significance":[],"alleles":["ACAGAGCTATATACTCAA","A"],"end":140554329,"strand":1,"feature_type":"variation","start":140554312,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1797272073","clinical_significance":[],"strand":1,"feature_type":"variation","end":140554314,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554314,"source":"dbSNP"},{"start":140554316,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140554316,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797272170","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797272279","clinical_significance":[],"start":140554317,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C","T"],"end":140554317,"strand":1,"feature_type":"variation"},{"alleles":["C","A"],"end":140554318,"feature_type":"variation","strand":1,"source":"dbSNP","start":140554318,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs985634954"},{"seq_region_name":"7","id":"rs1298359538","clinical_significance":[],"strand":1,"feature_type":"variation","end":140554320,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554320,"source":"dbSNP"},{"clinical_significance":[],"id":"rs777498745","seq_region_name":"7","source":"dbSNP","start":140554323,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140554323,"alleles":["T","C"],"feature_type":"variation","strand":1},{"start":140554324,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140554325,"alleles":["AC","ACAC"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797272731","clinical_significance":[]},{"start":140554328,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140554328,"alleles":["A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797272841","clinical_significance":[]},{"start":140554329,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140554329,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs925698902","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554332,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140554332,"clinical_significance":[],"seq_region_name":"7","id":"rs1797273013"},{"seq_region_name":"7","id":"rs1420814565","clinical_significance":[],"start":140554333,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140554333,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1797273307","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554344,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140554344},{"seq_region_name":"7","id":"rs1022587775","clinical_significance":[],"alleles":["A","G"],"end":140554346,"strand":1,"feature_type":"variation","start":140554346,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["T","C"],"end":140554347,"strand":1,"feature_type":"variation","start":140554347,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1238473589","clinical_significance":[]},{"clinical_significance":[],"id":"rs372815065","seq_region_name":"7","alleles":["T","C"],"end":140554348,"feature_type":"variation","strand":1,"source":"dbSNP","start":140554348,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs978300286","clinical_significance":[],"start":140554352,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140554352,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs753651222","end":140554359,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140554359,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554365,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140554365,"seq_region_name":"7","id":"rs376244259","clinical_significance":[]},{"seq_region_name":"7","id":"rs1441608481","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554366,"source":"dbSNP","strand":1,"feature_type":"variation","end":140554366,"alleles":["G","A","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554367,"source":"dbSNP","strand":1,"feature_type":"variation","end":140554367,"alleles":["C","A","T"],"seq_region_name":"7","id":"rs111364978","clinical_significance":[]},{"end":140554368,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140554368,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs916312346"},{"source":"dbSNP","start":140554375,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140554375,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1797274471","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1797274679","clinical_significance":[],"strand":1,"feature_type":"variation","end":140554376,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554376,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140554377,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554377,"source":"dbSNP","id":"rs947918792","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140554378,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140554378,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs553585904"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1337519938","source":"dbSNP","start":140554379,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140554379,"alleles":["C","T"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554379,"feature_type":"variation","strand":1,"end":140554383,"alleles":["CCTAT","-"],"clinical_significance":[],"seq_region_name":"7","id":"rs1234009681"},{"seq_region_name":"7","id":"rs1585617069","clinical_significance":[],"strand":1,"feature_type":"variation","end":140554382,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554382,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140554384,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554384,"clinical_significance":[],"seq_region_name":"7","id":"rs1797275310"},{"seq_region_name":"7","id":"rs1459993298","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554390,"source":"dbSNP","strand":1,"feature_type":"variation","end":140554390,"alleles":["A","T"]},{"alleles":["G","A"],"end":140554391,"strand":1,"feature_type":"variation","start":140554391,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1164450710","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs937329406","end":140554392,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140554392,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","G"],"end":140554394,"feature_type":"variation","strand":1,"source":"dbSNP","start":140554394,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1049640733","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140554396,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554396,"clinical_significance":[],"seq_region_name":"7","id":"rs887575310"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1397681450","source":"dbSNP","start":140554397,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140554397,"alleles":["T","A"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140554405,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140554405,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1392875347"},{"seq_region_name":"7","id":"rs745359705","clinical_significance":[],"start":140554406,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140554406,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1797276230","seq_region_name":"7","source":"dbSNP","start":140554408,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140554408,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs940632710","seq_region_name":"7","source":"dbSNP","start":140554409,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140554409,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1797276429","clinical_significance":[],"alleles":["T","C","G"],"end":140554410,"strand":1,"feature_type":"variation","start":140554410,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1797276547","seq_region_name":"7","clinical_significance":[],"start":140554413,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140554413,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"alleles":["GTGGATCACTTGAGGTCAGTTTG","G"],"end":140554435,"strand":1,"feature_type":"variation","start":140554413,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1797276650","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585617177","clinical_significance":[],"alleles":["T","G"],"end":140554414,"strand":1,"feature_type":"variation","start":140554414,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1461532923","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140554417,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554417},{"strand":1,"feature_type":"variation","end":140554418,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554418,"source":"dbSNP","seq_region_name":"7","id":"rs1005502037","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs866020865","alleles":["T","C"],"end":140554422,"feature_type":"variation","strand":1,"source":"dbSNP","start":140554422,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140554426,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554426,"clinical_significance":[],"seq_region_name":"7","id":"rs1036525880"},{"seq_region_name":"7","id":"rs1797277243","clinical_significance":[],"start":140554429,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140554429,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1797277350","clinical_significance":[],"end":140554431,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140554431,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1797277447","clinical_significance":[],"start":140554432,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140554432,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140554438,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554438,"clinical_significance":[],"seq_region_name":"7","id":"rs1797277550"},{"start":140554441,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140554440,"alleles":["-","G"],"strand":1,"feature_type":"variation","id":"rs1797277657","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1326631577","seq_region_name":"7","source":"dbSNP","start":140554444,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140554444,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1797277878","seq_region_name":"7","source":"dbSNP","start":140554447,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140554447,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140554448,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140554448,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1585617248","seq_region_name":"7"},{"clinical_significance":[],"id":"rs2130553465","seq_region_name":"7","alleles":["T","C"],"end":140554452,"feature_type":"variation","strand":1,"source":"dbSNP","start":140554452,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1797278075","seq_region_name":"7","clinical_significance":[],"start":140554453,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140554453,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554454,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140554454,"clinical_significance":[],"seq_region_name":"7","id":"rs1036210780"},{"seq_region_name":"7","id":"rs1797278290","clinical_significance":[],"start":140554455,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140554455,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1797278397","clinical_significance":[],"strand":1,"feature_type":"variation","end":140554457,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554457,"source":"dbSNP"},{"clinical_significance":[],"id":"rs34391556","seq_region_name":"7","feature_type":"variation","strand":1,"end":140554465,"alleles":["CCCC","CC","CCCCC"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554462},{"clinical_significance":[],"seq_region_name":"7","id":"rs1416792956","end":140554463,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140554463,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554475,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140554475,"id":"rs1797278740","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1415330473","clinical_significance":[],"strand":1,"feature_type":"variation","end":140554477,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554477,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554481,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140554481,"seq_region_name":"7","id":"rs897178338","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797279065","source":"dbSNP","start":140554493,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140554493,"feature_type":"variation","strand":1},{"end":140554496,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140554496,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs998179726","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1332020358","source":"dbSNP","start":140554497,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140554497,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs771664697","source":"dbSNP","start":140554500,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140554500,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1797279494","clinical_significance":[],"end":140554503,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140554503,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554506,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140554506,"id":"rs187763458","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554507,"source":"dbSNP","strand":1,"feature_type":"variation","end":140554507,"alleles":["G","A"],"seq_region_name":"7","id":"rs889870000","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140554508,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554508,"source":"dbSNP","seq_region_name":"7","id":"rs567820590","clinical_significance":[]},{"id":"rs1352047581","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554513,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140554513},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554514,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140554514,"clinical_significance":[],"id":"rs1022473831","seq_region_name":"7"},{"alleles":["A","G"],"end":140554516,"strand":1,"feature_type":"variation","start":140554516,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1197861162","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554518,"feature_type":"variation","strand":1,"end":140554518,"alleles":["G","A","C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs747511998"},{"clinical_significance":[],"id":"rs192386109","seq_region_name":"7","end":140554525,"alleles":["A","C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140554525,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs553647767","clinical_significance":[],"strand":1,"feature_type":"variation","end":140554526,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554526,"source":"dbSNP"},{"id":"rs960673973","seq_region_name":"7","clinical_significance":[],"start":140554531,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140554531,"strand":1,"feature_type":"variation"},{"start":140554536,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140554536,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797280654","clinical_significance":[]},{"alleles":["T","A"],"end":140554538,"strand":1,"feature_type":"variation","start":140554538,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1441236542","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1372538270","alleles":["C","A","G"],"end":140554543,"feature_type":"variation","strand":1,"source":"dbSNP","start":140554543,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797280981","feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140554544,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554544},{"seq_region_name":"7","id":"rs143616546","clinical_significance":[],"start":140554548,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140554548,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140554551,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554551,"source":"dbSNP","id":"rs1260288069","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1474248091","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554556,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140554556},{"seq_region_name":"7","id":"rs1385617299","clinical_significance":[],"start":140554558,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140554558,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554560,"feature_type":"variation","strand":1,"end":140554560,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs916348410"},{"start":140554561,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C"],"end":140554561,"strand":1,"feature_type":"variation","id":"rs539558995","seq_region_name":"7","clinical_significance":[]},{"start":140554562,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140554562,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs1797281750","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1006546642","clinical_significance":[],"alleles":["G","A"],"end":140554563,"strand":1,"feature_type":"variation","start":140554563,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140554566,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C","T"],"end":140554566,"strand":1,"feature_type":"variation","id":"rs1797281978","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs6965412","feature_type":"variation","strand":1,"end":140554567,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554567},{"clinical_significance":[],"id":"rs2130553794","seq_region_name":"7","source":"dbSNP","start":140554571,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140554571,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797282189","end":140554572,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140554572,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs984484579","clinical_significance":[],"start":140554580,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140554580,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs148083337","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554582,"feature_type":"variation","strand":1,"end":140554582,"alleles":["G","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1194499765","end":140554583,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140554583,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs909065611","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554584,"source":"dbSNP","strand":1,"feature_type":"variation","end":140554584,"alleles":["C","T"]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140554585,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554585,"clinical_significance":[],"seq_region_name":"7","id":"rs940516472"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554586,"feature_type":"variation","strand":1,"end":140554586,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs575994388"},{"clinical_significance":[],"id":"rs1036263104","seq_region_name":"7","source":"dbSNP","start":140554588,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140554588,"alleles":["A","G"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140554590,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140554590,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1165871157"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140554591,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554591,"clinical_significance":[],"seq_region_name":"7","id":"rs1244996205"},{"id":"rs1395503809","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554592,"source":"dbSNP","strand":1,"feature_type":"variation","end":140554592,"alleles":["C","T"]},{"start":140554592,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140554602,"alleles":["CACCACTACAC","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1198251419","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140554593,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554593,"clinical_significance":[],"seq_region_name":"7","id":"rs1797283431"},{"clinical_significance":[],"seq_region_name":"7","id":"rs543012342","feature_type":"variation","strand":1,"end":140554597,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554597},{"start":140554599,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140554599,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1286984867","clinical_significance":[]},{"seq_region_name":"7","id":"rs182531328","clinical_significance":[],"strand":1,"feature_type":"variation","end":140554605,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554605,"source":"dbSNP"},{"id":"rs1797283906","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140554606,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554606,"source":"dbSNP"},{"end":140554609,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140554609,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797284035"},{"seq_region_name":"7","id":"rs1797284141","clinical_significance":[],"strand":1,"feature_type":"variation","end":140554611,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554611,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140554613,"alleles":["GGG","GG"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554611,"source":"dbSNP","id":"rs1353531035","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs934019999","end":140554613,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140554613,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554614,"feature_type":"variation","strand":1,"end":140554614,"alleles":["T","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs542536216"},{"clinical_significance":[],"seq_region_name":"7","id":"rs187186300","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554617,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140554617},{"end":140554621,"alleles":["AGAG","-"],"strand":1,"feature_type":"variation","start":140554618,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797284743","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140554619,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554619,"source":"dbSNP","seq_region_name":"7","id":"rs1797284848","clinical_significance":[]},{"source":"dbSNP","start":140554623,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140554623,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1272508599"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554625,"source":"dbSNP","strand":1,"feature_type":"variation","end":140554625,"alleles":["G","C"],"seq_region_name":"7","id":"rs1797285046","clinical_significance":[]},{"end":140554633,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140554633,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1435155600"},{"clinical_significance":[],"seq_region_name":"7","id":"rs971179001","source":"dbSNP","start":140554636,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AAAAAAA","AAAAAA","AAAAAAAA"],"end":140554642,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1398140693","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140554638,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554638,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1359647989","clinical_significance":[],"start":140554643,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140554643,"alleles":["G","-"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797285534","end":140554643,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140554643,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554644,"source":"dbSNP","strand":1,"feature_type":"variation","end":140554651,"alleles":["AAAAAAAA","AAAAAAA","AAAAAAAAA"],"seq_region_name":"7","id":"rs1174042682","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797285981","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140554648,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554648,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554650,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140554650,"seq_region_name":"7","id":"rs1436743674","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585617784","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554666,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140554666},{"seq_region_name":"7","id":"rs981337295","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140554670,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554670,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140554676,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554676,"source":"dbSNP","id":"rs1797286309","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs889745780","clinical_significance":[],"strand":1,"feature_type":"variation","end":140554679,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554679,"source":"dbSNP"},{"id":"rs2130554114","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554683,"source":"dbSNP","strand":1,"feature_type":"variation","end":140554683,"alleles":["C","A"]},{"seq_region_name":"7","id":"rs1475770897","clinical_significance":[],"start":140554685,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140554685,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554692,"source":"dbSNP","strand":1,"feature_type":"variation","end":140554692,"alleles":["A","C","T"],"seq_region_name":"7","id":"rs1243957822","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554694,"source":"dbSNP","strand":1,"feature_type":"variation","end":140554694,"alleles":["G","A","T"],"id":"rs1797286709","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140554696,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554696,"source":"dbSNP","seq_region_name":"7","id":"rs1250466569","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140554702,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554702,"source":"dbSNP","seq_region_name":"7","id":"rs1006998365","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797287058","source":"dbSNP","start":140554705,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140554705,"feature_type":"variation","strand":1},{"end":140554708,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140554708,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs540905722","clinical_significance":[]},{"seq_region_name":"7","id":"rs1258590389","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140554709,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554709,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1043802873","alleles":["C","A"],"end":140554710,"feature_type":"variation","strand":1,"source":"dbSNP","start":140554710,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["T","G"],"end":140554712,"strand":1,"feature_type":"variation","start":140554712,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs904049639","clinical_significance":[]},{"seq_region_name":"7","id":"rs1313533477","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140554717,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554717,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1797287598","clinical_significance":[],"strand":1,"feature_type":"variation","end":140554720,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554720,"source":"dbSNP"},{"clinical_significance":[],"id":"rs73491542","seq_region_name":"7","alleles":["A","G"],"end":140554724,"feature_type":"variation","strand":1,"source":"dbSNP","start":140554724,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["GG","G"],"end":140554733,"strand":1,"feature_type":"variation","start":140554732,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1797287844","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554734,"feature_type":"variation","strand":1,"end":140554734,"alleles":["A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1797287965"},{"seq_region_name":"7","id":"rs1031708251","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554735,"source":"dbSNP","strand":1,"feature_type":"variation","end":140554735,"alleles":["T","C","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797288236","source":"dbSNP","start":140554738,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140554738,"alleles":["T","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1271489126","clinical_significance":[],"start":140554742,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140554742,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1216660569","seq_region_name":"7","source":"dbSNP","start":140554744,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140554744,"alleles":["T","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797288534","alleles":["TATATA","TA"],"end":140554754,"feature_type":"variation","strand":1,"source":"dbSNP","start":140554749,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140554750,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554750,"source":"dbSNP","seq_region_name":"7","id":"rs1797288640","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797288744","source":"dbSNP","start":140554753,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140554753,"alleles":["T","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1262522936","feature_type":"variation","strand":1,"end":140554755,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554755},{"source":"dbSNP","start":140554758,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140554758,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797288952"},{"clinical_significance":[],"id":"rs1797289066","seq_region_name":"7","feature_type":"variation","strand":1,"end":140554765,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554765},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554768,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140554768,"clinical_significance":[],"seq_region_name":"7","id":"rs940794924"},{"seq_region_name":"7","id":"rs2130554328","clinical_significance":[],"start":140554768,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["CC","C"],"end":140554769,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1430448979","clinical_significance":[],"end":140554769,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140554769,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs960977533","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554770,"feature_type":"variation","strand":1,"end":140554770,"alleles":["G","A","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1191289028","alleles":["G","A","C"],"end":140554773,"feature_type":"variation","strand":1,"source":"dbSNP","start":140554773,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797289687","alleles":["G","A"],"end":140554776,"feature_type":"variation","strand":1,"source":"dbSNP","start":140554776,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs2130554384","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140554779,"strand":1,"feature_type":"variation","start":140554779,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1797289773","seq_region_name":"7","clinical_significance":[],"alleles":["G","C"],"end":140554781,"strand":1,"feature_type":"variation","start":140554781,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140554783,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140554783,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1410808480"},{"alleles":["A","G"],"end":140554785,"feature_type":"variation","strand":1,"source":"dbSNP","start":140554785,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130554411"},{"alleles":["T","C"],"end":140554791,"strand":1,"feature_type":"variation","start":140554791,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1797289972","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554793,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140554793,"clinical_significance":[],"seq_region_name":"7","id":"rs1014217859"},{"source":"dbSNP","start":140554794,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140554794,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs770127898"},{"clinical_significance":[],"seq_region_name":"7","id":"rs968999711","feature_type":"variation","strand":1,"end":140554796,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554796},{"strand":1,"feature_type":"variation","end":140554803,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554803,"source":"dbSNP","id":"rs1797290488","seq_region_name":"7","clinical_significance":[]},{"start":140554805,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140554805,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797290603","clinical_significance":[]},{"seq_region_name":"7","id":"rs984535462","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140554806,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554806,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs908949392","source":"dbSNP","start":140554807,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140554807,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs376041059","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554808,"feature_type":"variation","strand":1,"end":140554808,"alleles":["G","A"]},{"id":"rs142730613","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554815,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140554815},{"seq_region_name":"7","id":"rs1434027581","clinical_significance":[],"start":140554823,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140554823,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140554824,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554824,"clinical_significance":[],"seq_region_name":"7","id":"rs1797291277"},{"strand":1,"feature_type":"variation","end":140554827,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554827,"source":"dbSNP","seq_region_name":"7","id":"rs1797291360","clinical_significance":[]},{"clinical_significance":[],"id":"rs1208966265","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554834,"feature_type":"variation","strand":1,"end":140554834,"alleles":["A","G","T"]},{"clinical_significance":[],"id":"rs1438061087","seq_region_name":"7","source":"dbSNP","start":140554835,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AAGAAGA","AAGA"],"end":140554841,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140554836,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140554836,"alleles":["A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797291723"},{"source":"dbSNP","start":140554837,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140554837,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1259353348"},{"strand":1,"feature_type":"variation","end":140554839,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554839,"source":"dbSNP","seq_region_name":"7","id":"rs2130554580","clinical_significance":[]},{"id":"rs74456849","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140554842,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554842,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs923063560","alleles":["C","G"],"end":140554843,"feature_type":"variation","strand":1,"source":"dbSNP","start":140554843,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1797292166","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554848,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140554848},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554850,"feature_type":"variation","strand":1,"end":140554850,"alleles":["T","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1797292281"},{"end":140554852,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140554852,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130554623"},{"seq_region_name":"7","id":"rs1293810532","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554857,"source":"dbSNP","strand":1,"feature_type":"variation","end":140554857,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1229998767","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554859,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140554859},{"source":"dbSNP","start":140554862,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140554862,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797292599"},{"seq_region_name":"7","id":"rs1050696284","clinical_significance":[],"alleles":["T","G"],"end":140554864,"strand":1,"feature_type":"variation","start":140554864,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs750949460","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554865,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140554865},{"seq_region_name":"7","id":"rs1386473897","clinical_significance":[],"end":140554867,"alleles":["AAA","AA"],"strand":1,"feature_type":"variation","start":140554865,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs192155933","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140554870,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554870,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563137001","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554871,"feature_type":"variation","strand":1,"end":140554871,"alleles":["A","AA"]},{"seq_region_name":"7","id":"rs1797293291","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554872,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140554872},{"start":140554874,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140554874,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs113620510","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1356500727","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140554875,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554875},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554876,"feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140554876,"clinical_significance":[],"seq_region_name":"7","id":"rs1329353487"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1007008139","source":"dbSNP","start":140554885,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140554885,"feature_type":"variation","strand":1},{"start":140554888,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140554888,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130554736","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1395361315","source":"dbSNP","start":140554893,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C","G"],"end":140554893,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140554894,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140554899,"alleles":["CCCCCC","CCCCC"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1032686083"},{"seq_region_name":"7","id":"rs184701109","clinical_significance":[],"strand":1,"feature_type":"variation","end":140554897,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554897,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1009957343","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554899,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140554899},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797294450","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554900,"feature_type":"variation","strand":1,"alleles":["T","-"],"end":140554900},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554901,"feature_type":"variation","strand":1,"end":140554901,"alleles":["C","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs138843217"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140554903,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554903,"clinical_significance":[],"seq_region_name":"7","id":"rs567644829"},{"clinical_significance":[],"id":"rs981221514","seq_region_name":"7","source":"dbSNP","start":140554909,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140554909,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1176450603","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554910,"feature_type":"variation","strand":1,"alleles":["TGT","T"],"end":140554912},{"alleles":["T","C"],"end":140554913,"feature_type":"variation","strand":1,"source":"dbSNP","start":140554913,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1456908935"},{"alleles":["T","A","C"],"end":140554915,"feature_type":"variation","strand":1,"source":"dbSNP","start":140554915,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs927251950","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1797294981","seq_region_name":"7","alleles":["T","C","G"],"end":140554917,"feature_type":"variation","strand":1,"source":"dbSNP","start":140554917,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1797295088","clinical_significance":[],"start":140554918,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140554918,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1223657354","alleles":["T","A","C"],"end":140554919,"feature_type":"variation","strand":1,"source":"dbSNP","start":140554919,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs528808622","end":140554920,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140554920,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1797295427","seq_region_name":"7","clinical_significance":[],"end":140554922,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140554922,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554923,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140554923,"clinical_significance":[],"id":"rs1043856088","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554928,"feature_type":"variation","strand":1,"end":140554928,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs903935280"},{"source":"dbSNP","start":140554929,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140554929,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797295730"},{"seq_region_name":"7","id":"rs1797295828","clinical_significance":[],"start":140554932,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140554932,"alleles":["T","G"],"strand":1,"feature_type":"variation"},{"end":140554934,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140554934,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130554926"},{"end":140554936,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140554936,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs369386320","seq_region_name":"7"},{"seq_region_name":"7","id":"rs766440591","clinical_significance":[],"strand":1,"feature_type":"variation","end":140554937,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554937,"source":"dbSNP"},{"seq_region_name":"7","id":"rs940664469","clinical_significance":[],"alleles":["C","G"],"end":140554944,"strand":1,"feature_type":"variation","start":140554944,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1052623196","clinical_significance":[],"end":140554945,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140554945,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797296379","alleles":["C","T"],"end":140554954,"feature_type":"variation","strand":1,"source":"dbSNP","start":140554954,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs896605786","source":"dbSNP","start":140554955,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140554955,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140554959,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554959,"clinical_significance":[],"id":"rs547283309","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1797296681","clinical_significance":[],"start":140554963,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140554963,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140554965,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554965,"clinical_significance":[],"seq_region_name":"7","id":"rs1486878128"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554972,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140554972,"clinical_significance":[],"seq_region_name":"7","id":"rs1295371237"},{"clinical_significance":[],"id":"rs1797296976","seq_region_name":"7","source":"dbSNP","start":140554975,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140554975,"alleles":["T","G"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140554977,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140554983,"alleles":["CACGCCA","CA"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797297074"},{"id":"rs142051392","seq_region_name":"7","clinical_significance":[],"end":140554979,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140554979,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["G","A"],"end":140554980,"strand":1,"feature_type":"variation","start":140554980,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs539190779","clinical_significance":[]},{"clinical_significance":[],"id":"rs1797297406","seq_region_name":"7","alleles":["C","T"],"end":140554981,"feature_type":"variation","strand":1,"source":"dbSNP","start":140554981,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1160226876","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140554983,"source":"dbSNP","strand":1,"feature_type":"variation","end":140554983,"alleles":["A","G"]},{"start":140554985,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140554985,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1024296856","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797297750","clinical_significance":[],"start":140554986,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140554986,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797297846","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140554988,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554988},{"source":"dbSNP","start":140554989,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140554989,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797297956"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1195207089","source":"dbSNP","start":140554990,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140554990,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs969051947","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140554992,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554992},{"clinical_significance":[],"id":"rs1393027690","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140554994,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140554994},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555000,"source":"dbSNP","strand":1,"feature_type":"variation","end":140555000,"alleles":["A","G"],"id":"rs557898095","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140555001,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140555001,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797298523"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797298641","feature_type":"variation","strand":1,"end":140555002,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555002},{"seq_region_name":"7","id":"rs1159711499","clinical_significance":[],"alleles":["CAATTCTCA","CA"],"end":140555011,"strand":1,"feature_type":"variation","start":140555003,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["A","G"],"end":140555005,"strand":1,"feature_type":"variation","start":140555005,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1050582438","clinical_significance":[]},{"clinical_significance":[],"id":"rs2130555152","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140555007,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555007},{"start":140555008,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140555008,"alleles":["C","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797298975","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797299089","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140555011,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555011,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555011,"feature_type":"variation","strand":1,"alleles":["AGAAGAAGAA","AGAAGAA"],"end":140555020,"clinical_significance":[],"seq_region_name":"7","id":"rs1253022266"},{"alleles":["A","T"],"end":140555020,"feature_type":"variation","strand":1,"source":"dbSNP","start":140555020,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1797299336","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1797299448","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["AAAA","AAA"],"end":140555028,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555025,"source":"dbSNP"},{"source":"dbSNP","start":140555026,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140555026,"alleles":["A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs889247221","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1016002644","source":"dbSNP","start":140555031,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140555031,"feature_type":"variation","strand":1},{"start":140555032,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140555032,"strand":1,"feature_type":"variation","id":"rs961778986","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130555214","clinical_significance":[],"start":140555033,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140555033,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs569691977","alleles":["G","A","T"],"end":140555034,"feature_type":"variation","strand":1,"source":"dbSNP","start":140555034,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555035,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140555035,"id":"rs1797299920","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555036,"source":"dbSNP","strand":1,"feature_type":"variation","end":140555036,"alleles":["A","C"],"seq_region_name":"7","id":"rs1563137166","clinical_significance":[]},{"seq_region_name":"7","id":"rs1246079042","clinical_significance":[],"end":140555038,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140555038,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797300274","feature_type":"variation","strand":1,"end":140555044,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555044},{"alleles":["G","A"],"end":140555045,"strand":1,"feature_type":"variation","start":140555045,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1216457718","clinical_significance":[]},{"id":"rs936940457","seq_region_name":"7","clinical_significance":[],"start":140555047,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140555047,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797300574","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555048,"feature_type":"variation","strand":1,"end":140555048,"alleles":["G","A"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555052,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140555052,"seq_region_name":"7","id":"rs1287803477","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555056,"feature_type":"variation","strand":1,"end":140555056,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1797300791"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1239618402","alleles":["A","C","G"],"end":140555057,"feature_type":"variation","strand":1,"source":"dbSNP","start":140555057,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs746286986","clinical_significance":[],"start":140555059,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140555059,"alleles":["C","G","T"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140555060,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555060,"clinical_significance":[],"seq_region_name":"7","id":"rs1797301141"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130555332","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555063,"feature_type":"variation","strand":1,"end":140555063,"alleles":["C","T"]},{"source":"dbSNP","start":140555064,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140555064,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1385179968"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140555065,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555065,"clinical_significance":[],"seq_region_name":"7","id":"rs1367055069"},{"source":"dbSNP","start":140555069,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140555069,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1797301434","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140555071,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555071,"clinical_significance":[],"id":"rs1289932444","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555077,"source":"dbSNP","strand":1,"feature_type":"variation","end":140555078,"alleles":["CA","CACA"],"seq_region_name":"7","id":"rs1402472988","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555078,"feature_type":"variation","strand":1,"end":140555078,"alleles":["A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs537148369"},{"end":140555080,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140555080,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1442655614","clinical_significance":[]},{"seq_region_name":"7","id":"rs1323559553","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555081,"source":"dbSNP","strand":1,"feature_type":"variation","end":140555081,"alleles":["T","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585618819","alleles":["T","C"],"end":140555083,"feature_type":"variation","strand":1,"source":"dbSNP","start":140555083,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1158434302","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140555084,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555084,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs554306391","feature_type":"variation","strand":1,"end":140555086,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555086},{"seq_region_name":"7","id":"rs1395343349","clinical_significance":[],"start":140555088,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140555088,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797302694","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555089,"feature_type":"variation","strand":1,"end":140555089,"alleles":["C","T"]},{"strand":1,"feature_type":"variation","alleles":["A","C","G","T"],"end":140555090,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555090,"source":"dbSNP","seq_region_name":"7","id":"rs4571657","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140555093,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555093,"clinical_significance":[],"seq_region_name":"7","id":"rs1308301884"},{"alleles":["C","T"],"end":140555102,"feature_type":"variation","strand":1,"source":"dbSNP","start":140555102,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1319287550"},{"start":140555106,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140555106,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1187020281","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555107,"source":"dbSNP","strand":1,"feature_type":"variation","end":140555107,"alleles":["A","C"],"seq_region_name":"7","id":"rs1797303389","clinical_significance":[]},{"end":140555113,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140555113,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1797303487","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1236915371","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555114,"source":"dbSNP","strand":1,"feature_type":"variation","end":140555114,"alleles":["G","A","C"]},{"feature_type":"variation","strand":1,"end":140555122,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555122,"clinical_significance":[],"seq_region_name":"7","id":"rs1797303755"},{"id":"rs986093269","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555127,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140555127},{"start":140555128,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140555128,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797303962","clinical_significance":[]},{"id":"rs1267606027","seq_region_name":"7","clinical_significance":[],"start":140555132,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C","G"],"end":140555132,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1585618974","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555134,"feature_type":"variation","strand":1,"end":140555134,"alleles":["T","C"]},{"alleles":["C","A"],"end":140555135,"feature_type":"variation","strand":1,"source":"dbSNP","start":140555135,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1797304283","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140555135,"alleles":["C","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555135,"clinical_significance":[],"id":"rs1797304374","seq_region_name":"7"},{"end":140555136,"alleles":["T","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140555136,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797304475"},{"clinical_significance":[],"id":"rs11308626","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555136,"feature_type":"variation","strand":1,"alleles":["TTTTTTTTTTTTTTTT","TTTTTTTTTTT","TTTTTTTTTTTT","TTTTTTTTTTTTT","TTTTTTTTTTTTTT","TTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTT"],"end":140555151},{"start":140555137,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140555137,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797305031","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1231389802","feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140555143,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555143},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585619019","source":"dbSNP","start":140555144,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140555144,"alleles":["T","C"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140555151,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555151,"source":"dbSNP","seq_region_name":"7","id":"rs1585619023","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797305468","clinical_significance":[],"alleles":["TG","-"],"end":140555152,"strand":1,"feature_type":"variation","start":140555151,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555152,"feature_type":"variation","strand":1,"alleles":["G","C","T"],"end":140555152,"clinical_significance":[],"id":"rs913944353","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1469013851","clinical_significance":[],"alleles":["G","-"],"end":140555152,"strand":1,"feature_type":"variation","start":140555152,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140555155,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555155,"clinical_significance":[],"id":"rs1020015384","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140555156,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555156,"source":"dbSNP","seq_region_name":"7","id":"rs1339102433","clinical_significance":[]},{"id":"rs150875492","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140555157,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555157,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797306129","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140555170,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555170},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797306211","end":140555174,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140555174,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1797306301","clinical_significance":[],"alleles":["G","C"],"end":140555179,"strand":1,"feature_type":"variation","start":140555179,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140555183,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555183,"clinical_significance":[],"seq_region_name":"7","id":"rs552820168"},{"seq_region_name":"7","id":"rs1177599682","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140555191,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555191,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1034195474","clinical_significance":[],"start":140555195,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140555195,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs942714940","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555196,"source":"dbSNP","strand":1,"feature_type":"variation","end":140555196,"alleles":["C","T"]},{"id":"rs979418036","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140555197,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555197,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1797306976","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555200,"source":"dbSNP","strand":1,"feature_type":"variation","end":140555200,"alleles":["C","A"]},{"id":"rs925237478","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140555202,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555202,"source":"dbSNP"},{"end":140555203,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140555203,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1376513713","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797307281","alleles":["C","G","T"],"end":140555205,"feature_type":"variation","strand":1,"source":"dbSNP","start":140555205,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1585619131","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555208,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140555208},{"seq_region_name":"7","id":"rs1797307630","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140555209,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555209,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1170773579","end":140555210,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140555210,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs958746268","clinical_significance":[],"end":140555212,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140555212,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140555214,"alleles":["A","C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555214,"source":"dbSNP","seq_region_name":"7","id":"rs984742930","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1475394104","end":140555218,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140555218,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs190333336","clinical_significance":[],"end":140555219,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140555219,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140555220,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555220,"clinical_significance":[],"seq_region_name":"7","id":"rs1052921487"},{"start":140555221,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140555221,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797309012","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555222,"source":"dbSNP","strand":1,"feature_type":"variation","end":140555222,"alleles":["C","T"],"seq_region_name":"7","id":"rs1797309142","clinical_significance":[]},{"start":140555226,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","T"],"end":140555226,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1250664027","clinical_significance":[]},{"id":"rs1162321440","seq_region_name":"7","clinical_significance":[],"start":140555227,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140555227,"alleles":["G","A","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1585619238","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140555228,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555228,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555229,"source":"dbSNP","strand":1,"feature_type":"variation","end":140555229,"alleles":["G","A"],"seq_region_name":"7","id":"rs1316547163","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555230,"feature_type":"variation","strand":1,"end":140555230,"alleles":["T","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585619250"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555231,"feature_type":"variation","strand":1,"end":140555231,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs896683396"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130555967","feature_type":"variation","strand":1,"end":140555233,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555233},{"seq_region_name":"7","id":"rs1797309912","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555235,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140555235},{"feature_type":"variation","strand":1,"end":140555242,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555242,"clinical_significance":[],"id":"rs949567413","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1797310117","clinical_significance":[],"start":140555250,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140555250,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1585619272","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555254,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140555254},{"feature_type":"variation","strand":1,"end":140555257,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555257,"clinical_significance":[],"seq_region_name":"7","id":"rs1797310340"},{"seq_region_name":"7","id":"rs1797310456","clinical_significance":[],"alleles":["T","A"],"end":140555258,"strand":1,"feature_type":"variation","start":140555258,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["G","A"],"end":140555259,"feature_type":"variation","strand":1,"source":"dbSNP","start":140555259,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1045361789"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797310646","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140555260,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555260},{"clinical_significance":[],"seq_region_name":"7","id":"rs1234487755","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555267,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140555267},{"clinical_significance":[],"seq_region_name":"7","id":"rs905446559","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555268,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140555268},{"alleles":["G","A"],"end":140555270,"strand":1,"feature_type":"variation","start":140555270,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1342619652","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130556080","source":"dbSNP","start":140555271,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140555271,"alleles":["T","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1797311063","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555272,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140555272},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555274,"feature_type":"variation","strand":1,"end":140555274,"alleles":["C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130556103"},{"seq_region_name":"7","id":"rs377441550","clinical_significance":[],"alleles":["G","A","T"],"end":140555276,"strand":1,"feature_type":"variation","start":140555276,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1006395758","clinical_significance":[],"alleles":["G","A"],"end":140555277,"strand":1,"feature_type":"variation","start":140555277,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140555278,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140555278,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1015885951"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1401089053","source":"dbSNP","start":140555279,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140555279,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797311607","feature_type":"variation","strand":1,"end":140555280,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555280},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797311717","source":"dbSNP","start":140555282,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140555282,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140555283,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140555283,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs897472969","seq_region_name":"7"},{"start":140555285,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140555285,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797311931","clinical_significance":[]},{"source":"dbSNP","start":140555289,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140555289,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1466712391","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["C","A","G","T"],"end":140555290,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555290,"clinical_significance":[],"id":"rs753630104","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1369921738","seq_region_name":"7","alleles":["G","A"],"end":140555291,"feature_type":"variation","strand":1,"source":"dbSNP","start":140555291,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1185149097","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140555292,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555292,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140555297,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555297,"clinical_significance":[],"seq_region_name":"7","id":"rs993272970"},{"source":"dbSNP","start":140555299,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140555299,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1251547548"},{"alleles":["T","A","C"],"end":140555301,"feature_type":"variation","strand":1,"source":"dbSNP","start":140555301,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1257566874"},{"source":"dbSNP","start":140555301,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140555310,"alleles":["TTTTTTTTTT","TTTTTTTTT","TTTTTTTTTTT"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs933386533"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1359076761","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555302,"feature_type":"variation","strand":1,"alleles":["T","A","G"],"end":140555302},{"seq_region_name":"7","id":"rs1264002430","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140555303,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555303,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555306,"source":"dbSNP","strand":1,"feature_type":"variation","end":140555306,"alleles":["T","G"],"seq_region_name":"7","id":"rs910737907","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1336774942","alleles":["T","G"],"end":140555310,"feature_type":"variation","strand":1,"source":"dbSNP","start":140555310,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1376098118","source":"dbSNP","start":140555311,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140555311,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1309487457","end":140555312,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140555312,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1390176721","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555313,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140555313},{"seq_region_name":"7","id":"rs1448619640","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["TTAGTAGGGATG","TTAGTAGGGATGTTAGTAGGGATG"],"end":140555328,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555317,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1030480416","seq_region_name":"7","source":"dbSNP","start":140555318,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140555318,"alleles":["T","C","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797313955","source":"dbSNP","start":140555320,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140555320,"alleles":["G","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs568050929","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140555323,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555323,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1585619549","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140555324,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555324},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140555325,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555325,"source":"dbSNP","seq_region_name":"7","id":"rs986365769","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555330,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140555330,"seq_region_name":"7","id":"rs535332811","clinical_significance":[]},{"end":140555337,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140555337,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1405816454"},{"id":"rs1797314596","seq_region_name":"7","clinical_significance":[],"start":140555338,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140555338,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1054068892","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140555339,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555339},{"clinical_significance":[],"seq_region_name":"7","id":"rs1392833136","alleles":["G","A"],"end":140555341,"feature_type":"variation","strand":1,"source":"dbSNP","start":140555341,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140555342,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555342,"clinical_significance":[],"id":"rs1585619594","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130556403","end":140555345,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140555345,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140555350,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140555350,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1797315015","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs563486435","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555353,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140555353},{"seq_region_name":"7","id":"rs1161196132","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555354,"source":"dbSNP","strand":1,"feature_type":"variation","end":140555354,"alleles":["G","T"]},{"clinical_significance":[],"id":"rs1017565399","seq_region_name":"7","feature_type":"variation","strand":1,"end":140555355,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555355},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797315463","feature_type":"variation","strand":1,"end":140555356,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555356},{"seq_region_name":"7","id":"rs968628264","clinical_significance":[],"end":140555358,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140555358,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140555359,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555359,"clinical_significance":[],"seq_region_name":"7","id":"rs1380728920"},{"start":140555361,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140555361,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585619646","clinical_significance":[]},{"seq_region_name":"7","id":"rs978634163","clinical_significance":[],"strand":1,"feature_type":"variation","end":140555364,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555364,"source":"dbSNP"},{"end":140555365,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140555365,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797315963","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797316078","end":140555366,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140555366,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs199679409","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555368,"source":"dbSNP","strand":1,"feature_type":"variation","end":140555368,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130556511","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555372,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140555372},{"source":"dbSNP","start":140555373,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140555373,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1438078352"},{"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140555381,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555381,"source":"dbSNP","seq_region_name":"7","id":"rs564967383","clinical_significance":[]},{"clinical_significance":[],"id":"rs1453780980","seq_region_name":"7","source":"dbSNP","start":140555382,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140555382,"alleles":["G","A"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140555385,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555385,"clinical_significance":[],"seq_region_name":"7","id":"rs575694579"},{"clinical_significance":[],"seq_region_name":"7","id":"rs543083530","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555386,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140555386},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797316930","end":140555393,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140555393,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs917994390","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555397,"source":"dbSNP","strand":1,"feature_type":"variation","end":140555397,"alleles":["C","T"]},{"end":140555402,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140555402,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797317125","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797317225","clinical_significance":[],"start":140555405,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140555405,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140555410,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140555410,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585619717"},{"clinical_significance":[],"seq_region_name":"7","id":"rs945754614","source":"dbSNP","start":140555413,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140555413,"alleles":["A","C"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140555419,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140555419,"alleles":["A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797317569"},{"end":140555420,"alleles":["T","C","G"],"strand":1,"feature_type":"variation","start":140555420,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1321372542","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","A","T"],"end":140555421,"strand":1,"feature_type":"variation","start":140555421,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs949614522","seq_region_name":"7","clinical_significance":[]},{"id":"rs966805207","seq_region_name":"7","clinical_significance":[],"start":140555426,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140555426,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1307849345","clinical_significance":[],"strand":1,"feature_type":"variation","end":140555427,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555427,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs35750288","feature_type":"variation","strand":1,"end":140555430,"alleles":["CCCC","CCC","CCCCC"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555427},{"clinical_significance":[],"seq_region_name":"7","id":"rs1045647921","source":"dbSNP","start":140555428,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140555428,"alleles":["C","T"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555429,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140555429,"seq_region_name":"7","id":"rs764778019","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs750134001","end":140555430,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140555430,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1797319042","seq_region_name":"7","source":"dbSNP","start":140555431,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140555431,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1041356407","clinical_significance":[],"alleles":["C","T"],"end":140555433,"strand":1,"feature_type":"variation","start":140555433,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555434,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140555434,"clinical_significance":[],"id":"rs906843025","seq_region_name":"7"},{"seq_region_name":"7","id":"rs2130556720","clinical_significance":[],"strand":1,"feature_type":"variation","end":140555436,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555436,"source":"dbSNP"},{"id":"rs2130556733","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140555437,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555437,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1797319578","seq_region_name":"7","alleles":["A","G"],"end":140555439,"feature_type":"variation","strand":1,"source":"dbSNP","start":140555439,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","G","T"],"end":140555441,"feature_type":"variation","strand":1,"source":"dbSNP","start":140555441,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs561157280","seq_region_name":"7"},{"end":140555442,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140555442,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs528469101","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs528864920","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555443,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140555443},{"feature_type":"variation","strand":1,"end":140555444,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555444,"clinical_significance":[],"id":"rs1181348178","seq_region_name":"7"},{"id":"rs1006455834","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555452,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140555452},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797320761","alleles":["C","G"],"end":140555453,"feature_type":"variation","strand":1,"source":"dbSNP","start":140555453,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140555454,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C","G"],"end":140555454,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs139383592"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1479030273","source":"dbSNP","start":140555456,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140555456,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140555462,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555462,"clinical_significance":[],"id":"rs1797321308","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140555463,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555463,"clinical_significance":[],"id":"rs1376060340","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1797321661","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555465,"source":"dbSNP","strand":1,"feature_type":"variation","end":140555465,"alleles":["G","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1475885813","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555469,"feature_type":"variation","strand":1,"end":140555469,"alleles":["C","T"]},{"clinical_significance":[],"id":"rs1797322023","seq_region_name":"7","alleles":["A","G"],"end":140555471,"feature_type":"variation","strand":1,"source":"dbSNP","start":140555471,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs2130556861","clinical_significance":[],"start":140555472,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140555472,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1797322177","seq_region_name":"7","end":140555473,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140555473,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555480,"source":"dbSNP","strand":1,"feature_type":"variation","end":140555480,"alleles":["G","A"],"id":"rs2130556888","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797322357","clinical_significance":[],"alleles":["T","C"],"end":140555483,"strand":1,"feature_type":"variation","start":140555483,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140555484,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555484,"source":"dbSNP","seq_region_name":"7","id":"rs1185203664","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130556918","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140555485,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555485,"source":"dbSNP"},{"id":"rs961954251","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140555486,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555486,"source":"dbSNP"},{"seq_region_name":"7","id":"rs2130556940","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140555487,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555487,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1214949555","feature_type":"variation","strand":1,"end":140555490,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555490},{"strand":1,"feature_type":"variation","end":140555497,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555497,"source":"dbSNP","seq_region_name":"7","id":"rs778458983","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797323223","clinical_significance":[],"end":140555499,"alleles":["A","-"],"strand":1,"feature_type":"variation","start":140555499,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["G","C"],"end":140555502,"feature_type":"variation","strand":1,"source":"dbSNP","start":140555502,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797323385"},{"clinical_significance":[],"id":"rs565539979","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140555503,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555503},{"seq_region_name":"7","id":"rs2130557000","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140555504,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555504,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1487076905","end":140555512,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140555512,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs543888721","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140555520,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555520,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797324168","source":"dbSNP","start":140555524,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140555524,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1346506983","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555530,"feature_type":"variation","strand":1,"end":140555530,"alleles":["T","C"]},{"id":"rs1272634481","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555532,"source":"dbSNP","strand":1,"feature_type":"variation","end":140555532,"alleles":["G","A"]},{"id":"rs1797324631","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140555534,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555534,"source":"dbSNP"},{"id":"rs1797324817","seq_region_name":"7","clinical_significance":[],"alleles":["-","TGAAGAGT"],"end":140555535,"strand":1,"feature_type":"variation","start":140555536,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1412563615","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555537,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","-"],"end":140555537},{"id":"rs1797324966","seq_region_name":"7","clinical_significance":[],"alleles":["T","C","G"],"end":140555537,"strand":1,"feature_type":"variation","start":140555537,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs779569380","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555541,"feature_type":"variation","strand":1,"end":140555541,"alleles":["A","T"]},{"seq_region_name":"7","id":"rs954668663","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555542,"source":"dbSNP","strand":1,"feature_type":"variation","end":140555542,"alleles":["T","A","C"]},{"end":140555544,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140555544,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797325798"},{"clinical_significance":[],"id":"rs986243630","seq_region_name":"7","source":"dbSNP","start":140555545,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140555545,"alleles":["T","A","C"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140555546,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555546,"clinical_significance":[],"seq_region_name":"7","id":"rs1797326197"},{"id":"rs1797326331","seq_region_name":"7","clinical_significance":[],"start":140555551,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140555551,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140555555,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140555555,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797326517"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555559,"source":"dbSNP","strand":1,"feature_type":"variation","end":140555559,"alleles":["C","T"],"seq_region_name":"7","id":"rs910612615","clinical_significance":[]},{"seq_region_name":"7","id":"rs149634983","clinical_significance":[],"alleles":["A","C","G"],"end":140555560,"strand":1,"feature_type":"variation","start":140555560,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["T","C"],"end":140555561,"strand":1,"feature_type":"variation","start":140555561,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1797327087","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140555562,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555562,"source":"dbSNP","id":"rs1797327241","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1171488777","alleles":["GGGGG","GGGG"],"end":140555566,"feature_type":"variation","strand":1,"source":"dbSNP","start":140555562,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140555563,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140555563,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs990052777"},{"id":"rs890192212","seq_region_name":"7","clinical_significance":[],"alleles":["G","T"],"end":140555564,"strand":1,"feature_type":"variation","start":140555564,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1007274141","seq_region_name":"7","clinical_significance":[],"alleles":["G","T"],"end":140555566,"strand":1,"feature_type":"variation","start":140555566,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1585620148","clinical_significance":[],"strand":1,"feature_type":"variation","end":140555567,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555567,"source":"dbSNP"},{"seq_region_name":"7","id":"rs193283204","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555568,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140555568},{"seq_region_name":"7","id":"rs1426439678","clinical_significance":[],"start":140555572,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140555572,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140555575,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555575,"source":"dbSNP","seq_region_name":"7","id":"rs1192189900","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs556757975","source":"dbSNP","start":140555580,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140555580,"alleles":["C","T"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140555583,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555583,"clinical_significance":[],"id":"rs1307923236","seq_region_name":"7"},{"source":"dbSNP","start":140555585,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AGAG","AG"],"end":140555588,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797329631"},{"source":"dbSNP","start":140555586,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140555586,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs750924984"},{"start":140555588,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140555588,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs1339585935","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1204204255","source":"dbSNP","start":140555589,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140555589,"alleles":["C","T"],"feature_type":"variation","strand":1},{"start":140555590,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140555590,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs968514192","clinical_significance":[]},{"clinical_significance":[],"id":"rs1361144527","seq_region_name":"7","alleles":["CCGTTCC","CCGTTCCGTTCC"],"end":140555600,"feature_type":"variation","strand":1,"source":"dbSNP","start":140555594,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140555595,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140555595,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs372001328"},{"clinical_significance":[],"seq_region_name":"7","id":"rs376614456","alleles":["G","A","T"],"end":140555596,"feature_type":"variation","strand":1,"source":"dbSNP","start":140555596,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs755174046","end":140555598,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140555598,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs201765167","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555602,"source":"dbSNP","strand":1,"feature_type":"variation","end":140555602,"alleles":["T","C"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555603,"source":"dbSNP","strand":1,"feature_type":"variation","end":140555603,"alleles":["C","T"],"seq_region_name":"7","id":"rs2130557353","clinical_significance":[]},{"seq_region_name":"7","id":"rs1318056435","clinical_significance":[],"strand":1,"feature_type":"variation","end":140555604,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555604,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1797331774","clinical_significance":[],"strand":1,"feature_type":"variation","end":140555609,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555609,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1279981036","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555609,"feature_type":"variation","strand":1,"end":140555612,"alleles":["CTCT","CT"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797332121","source":"dbSNP","start":140555612,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140555612,"alleles":["T","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs779096065","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555615,"feature_type":"variation","strand":1,"end":140555615,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797332479","end":140555616,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140555616,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1450219624","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555618,"source":"dbSNP","strand":1,"feature_type":"variation","end":140555618,"alleles":["T","G"]},{"seq_region_name":"7","id":"rs1563137693","clinical_significance":[],"start":140555620,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140555620,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs540862663","end":140555621,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140555621,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs768051689","source":"dbSNP","start":140555621,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140555622,"alleles":["GG","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1190555667","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555622,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140555622},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555625,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["-","G"],"end":140555624,"seq_region_name":"7","id":"rs1388577470","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140555625,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555625,"source":"dbSNP","seq_region_name":"7","id":"rs748438234","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555627,"source":"dbSNP","strand":1,"feature_type":"variation","end":140555627,"alleles":["A","G","T"],"seq_region_name":"7","id":"rs368694557","clinical_significance":[]},{"seq_region_name":"7","id":"rs536781743","clinical_significance":[],"alleles":["G","A"],"end":140555628,"strand":1,"feature_type":"variation","start":140555628,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_region_variant"},{"feature_type":"variation","strand":1,"end":140555629,"alleles":["T","C"],"consequence_type":"splice_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555629,"clinical_significance":[],"seq_region_name":"7","id":"rs1361333223"},{"start":140555631,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_donor_5th_base_variant","end":140555631,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1464847776","clinical_significance":[]},{"clinical_significance":[],"id":"rs2130557493","seq_region_name":"7","source":"dbSNP","start":140555633,"consequence_type":"splice_donor_region_variant","assembly_name":"GRCh38","end":140555633,"alleles":["C","G"],"feature_type":"variation","strand":1},{"alleles":["A","C"],"end":140555634,"strand":1,"feature_type":"variation","start":140555634,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_donor_variant","seq_region_name":"7","id":"rs1797334507","clinical_significance":[]},{"source":"dbSNP","start":140555635,"consequence_type":"splice_donor_variant","assembly_name":"GRCh38","end":140555635,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1055578292"},{"end":140555636,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140555636,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_region_variant","id":"rs745768435","seq_region_name":"7","clinical_significance":[]},{"start":140555637,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["C","T"],"end":140555637,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs769651180","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140555639,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140555639,"source":"dbSNP","seq_region_name":"7","id":"rs1338957353","clinical_significance":[]},{"clinical_significance":[],"id":"rs1333535810","seq_region_name":"7","alleles":["G","A"],"end":140555648,"feature_type":"variation","strand":1,"source":"dbSNP","start":140555648,"consequence_type":"synonymous_variant","assembly_name":"GRCh38"},{"start":140555649,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["C","T"],"end":140555649,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs775286405","clinical_significance":[]},{"clinical_significance":[],"id":"rs1797335792","seq_region_name":"7","end":140555654,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140555654,"consequence_type":"synonymous_variant","assembly_name":"GRCh38"},{"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555657,"feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140555657,"clinical_significance":[],"seq_region_name":"7","id":"rs755476225"},{"id":"rs1797336277","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140555659,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140555659,"source":"dbSNP"},{"end":140555662,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140555662,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs768627231","clinical_significance":[]},{"start":140555664,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140555664,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs562738531","clinical_significance":[]},{"clinical_significance":["uncertain significance"],"seq_region_name":"7","id":"rs771681826","end":140555665,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140555665,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140555671,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555671,"clinical_significance":[],"seq_region_name":"7","id":"rs1169162569"},{"seq_region_name":"7","id":"rs772883859","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140555687,"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140555687,"source":"dbSNP"},{"end":140555690,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140555690,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs766812190","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1797337749","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140555691,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140555691},{"alleles":["G","C","T"],"end":140555693,"feature_type":"variation","strand":1,"source":"dbSNP","start":140555693,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs201464750"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1255378443","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555694,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140555694},{"seq_region_name":"7","id":"rs754429763","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140555695,"source":"dbSNP","strand":1,"feature_type":"variation","end":140555695,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs759816693","clinical_significance":[],"end":140555697,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140555697,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"feature_type":"variation","strand":1,"end":140555698,"alleles":["T","C"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555698,"clinical_significance":[],"seq_region_name":"7","id":"rs917892042"},{"clinical_significance":[],"seq_region_name":"7","id":"rs765632778","source":"dbSNP","start":140555700,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140555700,"alleles":["C","A"],"feature_type":"variation","strand":1},{"alleles":["C","T"],"end":140555701,"strand":1,"feature_type":"variation","start":140555701,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs1464499737","clinical_significance":[]},{"seq_region_name":"7","id":"rs374490604","clinical_significance":["uncertain significance"],"start":140555704,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["T","G"],"end":140555704,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140555705,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140555705,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130557740"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1235359150","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555706,"feature_type":"variation","strand":1,"end":140555706,"alleles":["C","T"]},{"start":140555707,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["C","T"],"end":140555707,"strand":1,"feature_type":"variation","id":"rs758642466","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1431844526","end":140555710,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140555710,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs777789241","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140555711,"assembly_name":"GRCh38","consequence_type":"splice_region_variant","start":140555711,"source":"dbSNP"},{"seq_region_name":"7","id":"rs751595620","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140555713,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140555713,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1459230499","alleles":["C","T"],"end":140555719,"feature_type":"variation","strand":1,"source":"dbSNP","start":140555719,"consequence_type":"splice_region_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs756019527","seq_region_name":"7","source":"dbSNP","start":140555720,"consequence_type":"splice_region_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140555720,"feature_type":"variation","strand":1},{"start":140555725,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_polypyrimidine_tract_variant","end":140555725,"alleles":["G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1554466911","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs757757651","feature_type":"variation","strand":1,"end":140555727,"alleles":["A","C"],"consequence_type":"splice_polypyrimidine_tract_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555727},{"source":"dbSNP","start":140555728,"consequence_type":"splice_polypyrimidine_tract_variant","assembly_name":"GRCh38","end":140555728,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1037932527"},{"start":140555729,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_polypyrimidine_tract_variant","end":140555729,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1563137898","clinical_significance":[]},{"seq_region_name":"7","id":"rs1385889058","clinical_significance":[],"strand":1,"feature_type":"variation","end":140555733,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555733,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs779842025","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555736,"feature_type":"variation","strand":1,"end":140555736,"alleles":["G","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1293798785","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555741,"feature_type":"variation","strand":1,"end":140555741,"alleles":["A","G"]},{"end":140555742,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140555742,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs749311245"},{"alleles":["T","C"],"end":140555748,"strand":1,"feature_type":"variation","start":140555748,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs768535539","clinical_significance":[]},{"id":"rs1797340994","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555750,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140555750},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555759,"feature_type":"variation","strand":1,"end":140555759,"alleles":["A","G"],"clinical_significance":[],"id":"rs1797341115","seq_region_name":"7"},{"id":"rs1290279215","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","-"],"end":140555765,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555765,"source":"dbSNP"},{"start":140555773,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140555773,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs897629932","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797341462","source":"dbSNP","start":140555773,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140555775,"alleles":["CCC","CC"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs942189635","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555775,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140555775},{"seq_region_name":"7","id":"rs144371506","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555778,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140555778},{"alleles":["AT","-"],"end":140555779,"feature_type":"variation","strand":1,"source":"dbSNP","start":140555778,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs2130557957","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797341828","feature_type":"variation","strand":1,"end":140555779,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555779},{"clinical_significance":[],"seq_region_name":"7","id":"rs1314595592","end":140555780,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140555780,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1447887510","feature_type":"variation","strand":1,"end":140555788,"alleles":["C","A","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555788},{"seq_region_name":"7","id":"rs1329414071","clinical_significance":[],"start":140555789,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140555789,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797342330","source":"dbSNP","start":140555799,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140555799,"feature_type":"variation","strand":1},{"end":140555803,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140555803,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585621044","clinical_significance":[]},{"seq_region_name":"7","id":"rs1208011738","clinical_significance":[],"start":140555807,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140555807,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555813,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140555813,"clinical_significance":[],"seq_region_name":"7","id":"rs919500311"},{"end":140555817,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140555817,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797342755"},{"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140555818,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555818,"clinical_significance":[],"seq_region_name":"7","id":"rs1030223293"},{"clinical_significance":[],"seq_region_name":"7","id":"rs929020723","alleles":["A","C"],"end":140555819,"feature_type":"variation","strand":1,"source":"dbSNP","start":140555819,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs954719117","clinical_significance":[],"alleles":["T","C"],"end":140555820,"strand":1,"feature_type":"variation","start":140555820,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1475486676","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555821,"feature_type":"variation","strand":1,"end":140555821,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs4342501","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555823,"feature_type":"variation","strand":1,"end":140555823,"alleles":["T","C"]},{"end":140555826,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140555826,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1417015050"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140555828,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555828,"clinical_significance":[],"id":"rs890085640","seq_region_name":"7"},{"id":"rs1162517823","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140555829,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555829,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140555832,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555832,"source":"dbSNP","seq_region_name":"7","id":"rs1797344137","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555835,"feature_type":"variation","strand":1,"end":140555835,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1017727199"},{"alleles":["C","T"],"end":140555836,"strand":1,"feature_type":"variation","start":140555836,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1568640","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1176274662","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555841,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140555841},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555846,"feature_type":"variation","strand":1,"end":140555846,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1480240740"},{"seq_region_name":"7","id":"rs1247193980","clinical_significance":[],"alleles":["G","A"],"end":140555849,"strand":1,"feature_type":"variation","start":140555849,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1797344830","clinical_significance":[],"end":140555852,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140555852,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1797344947","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555855,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140555855},{"end":140555856,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140555856,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797345051","clinical_significance":[]},{"seq_region_name":"7","id":"rs11763409","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140555857,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555857,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555862,"source":"dbSNP","strand":1,"feature_type":"variation","end":140555862,"alleles":["T","G"],"id":"rs1319702032","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs914074764","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555865,"feature_type":"variation","strand":1,"end":140555865,"alleles":["G","A"]},{"id":"rs1376525862","seq_region_name":"7","clinical_significance":[],"start":140555866,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140555866,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1797345689","clinical_significance":[],"end":140555873,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140555873,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1356134161","clinical_significance":[],"start":140555876,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140555876,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555877,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140555877,"clinical_significance":[],"id":"rs1797345902","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140555878,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555878,"clinical_significance":[],"seq_region_name":"7","id":"rs1797346022"},{"start":140555880,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A","C"],"end":140555880,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1437139997","clinical_significance":[]},{"end":140555885,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140555885,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1223268333"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555886,"feature_type":"variation","strand":1,"end":140555887,"alleles":["AA","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1368445494"},{"end":140555890,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140555890,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1295795655","seq_region_name":"7"},{"source":"dbSNP","start":140555895,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140555895,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs904382812"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1435020079","feature_type":"variation","strand":1,"end":140555897,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555897},{"clinical_significance":[],"seq_region_name":"7","id":"rs773478425","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555899,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140555899},{"start":140555903,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140555903,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1299192641","clinical_significance":[]},{"seq_region_name":"7","id":"rs982342139","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555906,"source":"dbSNP","strand":1,"feature_type":"variation","end":140555906,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1797347241","clinical_significance":[],"start":140555908,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TTT","TT"],"end":140555910,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140555911,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555911,"clinical_significance":[],"id":"rs1358649458","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555914,"source":"dbSNP","strand":1,"feature_type":"variation","end":140555914,"alleles":["A","C"],"id":"rs749475575","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555916,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140555916,"seq_region_name":"7","id":"rs1031630124","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140555921,"alleles":["ATGAT","AT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555917,"source":"dbSNP","id":"rs1156511192","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797347946","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555918,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140555918},{"source":"dbSNP","start":140555922,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140555922,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797348057"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555925,"source":"dbSNP","strand":1,"feature_type":"variation","end":140555925,"alleles":["T","C"],"id":"rs577554518","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1425345233","alleles":["T","C"],"end":140555926,"feature_type":"variation","strand":1,"source":"dbSNP","start":140555926,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140555934,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140555934,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1192839584","clinical_significance":[]},{"end":140555939,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140555939,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1487474846","clinical_significance":[]},{"seq_region_name":"7","id":"rs1055868528","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555946,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140555946},{"seq_region_name":"7","id":"rs1797348690","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555950,"source":"dbSNP","strand":1,"feature_type":"variation","end":140555953,"alleles":["ATCT","-"]},{"id":"rs1014133904","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140555952,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555952,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1025414845","clinical_significance":[],"alleles":["T","C"],"end":140555954,"strand":1,"feature_type":"variation","start":140555954,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["T","G"],"end":140555955,"feature_type":"variation","strand":1,"source":"dbSNP","start":140555955,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs970725611"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1489175125","source":"dbSNP","start":140555959,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140555959,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140555962,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140555962,"alleles":["A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797349248"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140555963,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555963,"source":"dbSNP","seq_region_name":"7","id":"rs1797349348","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797349450","end":140555964,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140555964,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797349543","feature_type":"variation","strand":1,"end":140555972,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555972},{"seq_region_name":"7","id":"rs1797349639","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555974,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140555974},{"seq_region_name":"7","id":"rs1585621510","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555987,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140555987},{"start":140555988,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AAAAAAAAA","AAAAAAA","AAAAAAAA","AAAAAAAAAA"],"end":140555996,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs915698637","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140555991,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555991,"clinical_significance":[],"seq_region_name":"7","id":"rs2130558556"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140555994,"feature_type":"variation","strand":1,"end":140555994,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs35810692"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1272120773","source":"dbSNP","start":140555997,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","-"],"end":140555997,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs141042780","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140555999,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140555999,"source":"dbSNP"},{"end":140556000,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140556000,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs926691267","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797350473","feature_type":"variation","strand":1,"end":140556002,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556002},{"id":"rs993314722","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556006,"source":"dbSNP","strand":1,"feature_type":"variation","end":140556006,"alleles":["A","G"]},{"clinical_significance":[],"id":"rs1402215864","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140556009,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556009},{"clinical_significance":[],"id":"rs1227342020","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556010,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140556010},{"start":140556010,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TTTTTTT","TTTTTTTT"],"end":140556016,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797350884","clinical_significance":[]},{"seq_region_name":"7","id":"rs1286753625","clinical_significance":[],"strand":1,"feature_type":"variation","end":140556012,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556012,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs538092279","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556013,"feature_type":"variation","strand":1,"alleles":["TTTTGTTTTGTTTTGTTTTGTTTTG","TTTTGTTTTGTTTTGTTTTG","TTTTGTTTTGTTTTGTTTTGTTTTGTTTTG"],"end":140556037},{"end":140556014,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140556014,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1303881052"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1349888553","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556017,"feature_type":"variation","strand":1,"end":140556017,"alleles":["G","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556018,"source":"dbSNP","strand":1,"feature_type":"variation","end":140556018,"alleles":["T","G"],"id":"rs1797351519","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556022,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C","T"],"end":140556022,"id":"rs771069279","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1277884866","clinical_significance":[],"strand":1,"feature_type":"variation","end":140556027,"alleles":["G","C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556027,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140556032,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556032,"clinical_significance":[],"id":"rs1797351928","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs185610955","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140556035,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556035},{"source":"dbSNP","start":140556036,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140556038,"alleles":["TGA","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs79687428"},{"seq_region_name":"7","id":"rs1447060865","clinical_significance":[],"strand":1,"feature_type":"variation","end":140556041,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556041,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140556043,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556043,"source":"dbSNP","id":"rs2130558737","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs973534457","feature_type":"variation","strand":1,"end":140556047,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556047},{"strand":1,"feature_type":"variation","alleles":["CTCACTC","CTC"],"end":140556053,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556047,"source":"dbSNP","id":"rs1797352450","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140556050,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140556050,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1428483182"},{"clinical_significance":[],"id":"rs919396959","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140556051,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556051},{"clinical_significance":[],"id":"rs1194347697","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556051,"feature_type":"variation","strand":1,"end":140556054,"alleles":["CTCT","CT"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556054,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140556054,"clinical_significance":[],"seq_region_name":"7","id":"rs1478676161"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140556057,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556057,"clinical_significance":[],"id":"rs879173206","seq_region_name":"7"},{"source":"dbSNP","start":140556062,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140556062,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797353129"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556069,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140556069,"id":"rs1260833106","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797353352","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556071,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140556071},{"strand":1,"feature_type":"variation","end":140556077,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556077,"source":"dbSNP","seq_region_name":"7","id":"rs1204712433","clinical_significance":[]},{"source":"dbSNP","start":140556078,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140556078,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130558846"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1007592732","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140556082,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556082},{"source":"dbSNP","start":140556084,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140556084,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs937965161","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140556086,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556086,"clinical_significance":[],"id":"rs1217344331","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140556089,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556089,"source":"dbSNP","seq_region_name":"7","id":"rs1585621832","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797353982","source":"dbSNP","start":140556094,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140556094,"alleles":["T","C"],"feature_type":"variation","strand":1},{"id":"rs1585621845","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140556098,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556098,"source":"dbSNP"},{"source":"dbSNP","start":140556099,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140556099,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797354181"},{"start":140556105,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140556105,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130558904","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130558912","clinical_significance":[],"strand":1,"feature_type":"variation","end":140556113,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556113,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797354288","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556114,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140556114},{"seq_region_name":"7","id":"rs1051996440","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556119,"source":"dbSNP","strand":1,"feature_type":"variation","end":140556119,"alleles":["G","C"]},{"strand":1,"feature_type":"variation","end":140556120,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556120,"source":"dbSNP","seq_region_name":"7","id":"rs377391123","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs774419454","end":140556121,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140556121,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1797354742","seq_region_name":"7","source":"dbSNP","start":140556123,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140556123,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1797354856","seq_region_name":"7","source":"dbSNP","start":140556125,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140556125,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1259232348","end":140556126,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140556126,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140556136,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556136,"source":"dbSNP","seq_region_name":"7","id":"rs1221074716","clinical_significance":[]},{"source":"dbSNP","start":140556142,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140556142,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs943000467"},{"seq_region_name":"7","id":"rs575377421","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140556149,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556149,"source":"dbSNP"},{"seq_region_name":"7","id":"rs2130558983","clinical_significance":[],"start":140556151,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140556151,"strand":1,"feature_type":"variation"},{"id":"rs1797355395","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140556152,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556152,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140556153,"alleles":["G","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556153,"clinical_significance":[],"seq_region_name":"7","id":"rs1381240198"},{"seq_region_name":"7","id":"rs1797355674","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556168,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140556168},{"alleles":["C","A"],"end":140556169,"strand":1,"feature_type":"variation","start":140556169,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs904267330","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1396057447","source":"dbSNP","start":140556174,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140556174,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs999915064","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556175,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140556175},{"strand":1,"feature_type":"variation","end":140556179,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556179,"source":"dbSNP","id":"rs2130559035","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140556180,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140556180,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130559047"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556182,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140556182,"seq_region_name":"7","id":"rs1797356183","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797356267","clinical_significance":[],"end":140556183,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140556183,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556190,"source":"dbSNP","strand":1,"feature_type":"variation","end":140556190,"alleles":["G","A"],"seq_region_name":"7","id":"rs1171303359","clinical_significance":[]},{"start":140556191,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140556191,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797356493","clinical_significance":[]},{"source":"dbSNP","start":140556193,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140556193,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1053365977"},{"source":"dbSNP","start":140556194,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140556194,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs891602931"},{"feature_type":"variation","strand":1,"end":140556195,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556195,"clinical_significance":[],"seq_region_name":"7","id":"rs1797356811"},{"seq_region_name":"7","id":"rs1014601435","clinical_significance":[],"end":140556202,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140556202,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1797357020","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556204,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140556204},{"id":"rs1024212971","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140556206,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556206,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797357245","source":"dbSNP","start":140556207,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140556207,"alleles":["G","A"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140556211,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556211,"clinical_significance":[],"seq_region_name":"7","id":"rs1425142492"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1401305980","feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140556214,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556214},{"seq_region_name":"7","id":"rs7782076","clinical_significance":[],"strand":1,"feature_type":"variation","end":140556215,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556215,"source":"dbSNP"},{"start":140556217,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140556217,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1002156402","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140556225,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556225,"source":"dbSNP","seq_region_name":"7","id":"rs1258504956","clinical_significance":[]},{"source":"dbSNP","start":140556228,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140556228,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs966878589"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556229,"source":"dbSNP","strand":1,"feature_type":"variation","end":140556229,"alleles":["G","T"],"seq_region_name":"7","id":"rs1797358081","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130559208","clinical_significance":[],"alleles":["T","C"],"end":140556231,"strand":1,"feature_type":"variation","start":140556231,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140556234,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140556234,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585622146"},{"clinical_significance":[],"id":"rs1434661387","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556237,"feature_type":"variation","strand":1,"end":140556237,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1033759675","clinical_significance":[],"alleles":["G","A","T"],"end":140556238,"strand":1,"feature_type":"variation","start":140556238,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797358555","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556240,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140556240},{"alleles":["C","G"],"end":140556243,"strand":1,"feature_type":"variation","start":140556243,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1201013213","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797358752","clinical_significance":[],"strand":1,"feature_type":"variation","end":140556246,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556246,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556248,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140556248,"clinical_significance":[],"seq_region_name":"7","id":"rs2130559276"},{"seq_region_name":"7","id":"rs561389684","clinical_significance":[],"alleles":["C","T"],"end":140556249,"strand":1,"feature_type":"variation","start":140556249,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs189287875","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556250,"source":"dbSNP","strand":1,"feature_type":"variation","end":140556250,"alleles":["T","A"]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140556251,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556251,"source":"dbSNP","seq_region_name":"7","id":"rs147564563","clinical_significance":[]},{"source":"dbSNP","start":140556252,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140556252,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1026915424"},{"seq_region_name":"7","id":"rs1797359168","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556261,"source":"dbSNP","strand":1,"feature_type":"variation","end":140556261,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1438509397","source":"dbSNP","start":140556262,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140556262,"feature_type":"variation","strand":1},{"end":140556263,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140556263,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1797359265","seq_region_name":"7"},{"source":"dbSNP","start":140556268,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140556268,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797359362"},{"alleles":["T","C"],"end":140556269,"feature_type":"variation","strand":1,"source":"dbSNP","start":140556269,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797359468"},{"alleles":["A","C"],"end":140556278,"feature_type":"variation","strand":1,"source":"dbSNP","start":140556278,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs180838841"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140556282,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556282,"clinical_significance":[],"seq_region_name":"7","id":"rs1797359688"},{"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140556287,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556287,"clinical_significance":[],"id":"rs1797359794","seq_region_name":"7"},{"source":"dbSNP","start":140556291,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140556291,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1797359896","seq_region_name":"7"},{"source":"dbSNP","start":140556294,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140556294,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797360005"},{"feature_type":"variation","strand":1,"end":140556300,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556300,"clinical_significance":[],"id":"rs2130559402","seq_region_name":"7"},{"alleles":["C","T"],"end":140556302,"feature_type":"variation","strand":1,"source":"dbSNP","start":140556302,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1314423252"},{"clinical_significance":[],"seq_region_name":"7","id":"rs915566675","source":"dbSNP","start":140556304,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140556304,"feature_type":"variation","strand":1},{"alleles":["C","T"],"end":140556307,"feature_type":"variation","strand":1,"source":"dbSNP","start":140556307,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs941674648"},{"id":"rs1797360451","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140556309,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556309,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1331440545","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140556310,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556310,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1448851103","feature_type":"variation","strand":1,"end":140556312,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556312},{"source":"dbSNP","start":140556313,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140556313,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797360759"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556320,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140556320,"clinical_significance":[],"seq_region_name":"7","id":"rs1797360871"},{"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140556321,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556321,"clinical_significance":[],"seq_region_name":"7","id":"rs988156352"},{"end":140556323,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140556323,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1167312558","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140556325,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556325,"source":"dbSNP","id":"rs1458193312","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556331,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140556331,"seq_region_name":"7","id":"rs185446961","clinical_significance":[]},{"id":"rs1797361450","seq_region_name":"7","clinical_significance":[],"alleles":["A","C"],"end":140556334,"strand":1,"feature_type":"variation","start":140556334,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs569953323","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556335,"source":"dbSNP","strand":1,"feature_type":"variation","end":140556335,"alleles":["A","C"]},{"seq_region_name":"7","id":"rs974416336","clinical_significance":[],"start":140556336,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140556336,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556337,"feature_type":"variation","strand":1,"end":140556341,"alleles":["TTTTT","TTTTTT"],"clinical_significance":[],"seq_region_name":"7","id":"rs1797361799"},{"seq_region_name":"7","id":"rs200735786","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556340,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140556340},{"clinical_significance":[],"id":"rs1180625532","seq_region_name":"7","source":"dbSNP","start":140556344,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140556344,"alleles":["T","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs943283348","clinical_significance":[],"alleles":["T","G"],"end":140556345,"strand":1,"feature_type":"variation","start":140556345,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797362223","alleles":["A","G"],"end":140556346,"feature_type":"variation","strand":1,"source":"dbSNP","start":140556346,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs562956560","alleles":["C","A","T"],"end":140556361,"feature_type":"variation","strand":1,"source":"dbSNP","start":140556361,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs935754936","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140556362,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556362,"source":"dbSNP"},{"source":"dbSNP","start":140556368,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140556368,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1052844360"},{"seq_region_name":"7","id":"rs891653800","clinical_significance":[],"strand":1,"feature_type":"variation","end":140556370,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556370,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1327937593","seq_region_name":"7","source":"dbSNP","start":140556371,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140556371,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797362804","source":"dbSNP","start":140556373,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140556373,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1797362908","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556378,"source":"dbSNP","strand":1,"feature_type":"variation","end":140556378,"alleles":["G","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556383,"source":"dbSNP","strand":1,"feature_type":"variation","end":140556383,"alleles":["G","C"],"id":"rs368280654","seq_region_name":"7","clinical_significance":[]},{"id":"rs1254539005","seq_region_name":"7","clinical_significance":[],"alleles":["A","G"],"end":140556384,"strand":1,"feature_type":"variation","start":140556384,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140556385,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140556385,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs553387157","seq_region_name":"7"},{"alleles":["T","G"],"end":140556386,"strand":1,"feature_type":"variation","start":140556386,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1197226874","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797363463","alleles":["G","A"],"end":140556388,"feature_type":"variation","strand":1,"source":"dbSNP","start":140556388,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["T","C","G"],"end":140556391,"strand":1,"feature_type":"variation","start":140556391,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs530905745","clinical_significance":[]},{"start":140556392,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140556392,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797363742","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs893812663","feature_type":"variation","strand":1,"end":140556393,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556393},{"strand":1,"feature_type":"variation","end":140556396,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556396,"source":"dbSNP","seq_region_name":"7","id":"rs140389551","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1021019537","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556397,"feature_type":"variation","strand":1,"end":140556397,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797364076","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140556398,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556398},{"alleles":["C","G","T"],"end":140556399,"strand":1,"feature_type":"variation","start":140556399,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs113884334","clinical_significance":[]},{"seq_region_name":"7","id":"rs113540957","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140556400,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556400,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140556401,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556401,"clinical_significance":[],"seq_region_name":"7","id":"rs528163839"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556402,"feature_type":"variation","strand":1,"end":140556402,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs140335722"},{"seq_region_name":"7","id":"rs1363368897","clinical_significance":[],"strand":1,"feature_type":"variation","end":140556404,"alleles":["T","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556404,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1200120297","feature_type":"variation","strand":1,"end":140556413,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556413},{"seq_region_name":"7","id":"rs1435441049","clinical_significance":[],"alleles":["C","T"],"end":140556414,"strand":1,"feature_type":"variation","start":140556414,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1267153226","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556415,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140556415},{"id":"rs2130559752","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140556417,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556417,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140556418,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556418,"source":"dbSNP","id":"rs1585622616","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs533275126","clinical_significance":[],"start":140556419,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140556419,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1222257613","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556420,"feature_type":"variation","strand":1,"end":140556420,"alleles":["C","A"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556423,"source":"dbSNP","strand":1,"feature_type":"variation","end":140556431,"alleles":["CCACTTCCC","C"],"seq_region_name":"7","id":"rs1384827723","clinical_significance":[]},{"start":140556425,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140556425,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1322660489","clinical_significance":[]},{"seq_region_name":"7","id":"rs959530506","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556426,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140556426},{"clinical_significance":[],"id":"rs950990089","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556432,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140556432},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140556433,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556433,"source":"dbSNP","id":"rs1797365955","seq_region_name":"7","clinical_significance":[]},{"start":140556439,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140556439,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1286257559","clinical_significance":[]},{"id":"rs1585622678","seq_region_name":"7","clinical_significance":[],"start":140556445,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140556445,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"end":140556447,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140556447,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs538578340","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["AG","-"],"end":140556457,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556456,"clinical_significance":[],"seq_region_name":"7","id":"rs1347916453"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556457,"feature_type":"variation","strand":1,"end":140556457,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130559864"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556458,"feature_type":"variation","strand":1,"end":140556458,"alleles":["C","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1278448687"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1233807474","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556459,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140556459},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556461,"source":"dbSNP","strand":1,"feature_type":"variation","end":140556461,"alleles":["C","T"],"seq_region_name":"7","id":"rs1797366680","clinical_significance":[]},{"end":140556462,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140556462,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797366786"},{"seq_region_name":"7","id":"rs4726895","clinical_significance":[],"strand":1,"feature_type":"variation","end":140556464,"alleles":["G","A","C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556464,"source":"dbSNP"},{"id":"rs568962687","seq_region_name":"7","clinical_significance":[],"alleles":["T","A","C"],"end":140556467,"strand":1,"feature_type":"variation","start":140556467,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs112474341","clinical_significance":[],"strand":1,"feature_type":"variation","end":140556468,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556468,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556470,"feature_type":"variation","strand":1,"end":140556470,"alleles":["C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1399182276"},{"feature_type":"variation","strand":1,"end":140556473,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556473,"clinical_significance":[],"seq_region_name":"7","id":"rs1384276727"},{"start":140556476,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140556477,"alleles":["TT","TTT"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs139631392","clinical_significance":[]},{"end":140556477,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140556477,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1332261415","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556482,"feature_type":"variation","strand":1,"end":140556482,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs925623420"},{"feature_type":"variation","strand":1,"end":140556483,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556483,"clinical_significance":[],"seq_region_name":"7","id":"rs929047155"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556484,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140556484,"seq_region_name":"7","id":"rs188704277","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556488,"source":"dbSNP","strand":1,"feature_type":"variation","end":140556488,"alleles":["G","A"],"seq_region_name":"7","id":"rs2130559988","clinical_significance":[]},{"id":"rs1797368215","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140556489,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556489,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs772384325","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556495,"feature_type":"variation","strand":1,"end":140556495,"alleles":["C","A","T"]},{"alleles":["G","A"],"end":140556496,"strand":1,"feature_type":"variation","start":140556496,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1289630007","clinical_significance":[]},{"id":"rs1797368578","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556497,"source":"dbSNP","strand":1,"feature_type":"variation","end":140556497,"alleles":["C","G","T"]},{"seq_region_name":"7","id":"rs911732830","clinical_significance":[],"alleles":["T","G"],"end":140556513,"strand":1,"feature_type":"variation","start":140556513,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556514,"source":"dbSNP","strand":1,"feature_type":"variation","end":140556514,"alleles":["A","G"],"seq_region_name":"7","id":"rs943189501","clinical_significance":[]},{"clinical_significance":[],"id":"rs1797368968","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556515,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140556515},{"alleles":["T","G"],"end":140556518,"strand":1,"feature_type":"variation","start":140556518,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1039392414","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140556522,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556522,"source":"dbSNP","seq_region_name":"7","id":"rs1261150394","clinical_significance":[]},{"start":140556526,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140556526,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1222903903","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140556528,"alleles":["T","A","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556528,"source":"dbSNP","seq_region_name":"7","id":"rs1329720378","clinical_significance":[]},{"start":140556529,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140556529,"alleles":["A","G"],"strand":1,"feature_type":"variation","id":"rs1428834621","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1326107039","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556530,"feature_type":"variation","strand":1,"end":140556532,"alleles":["GGG","GG"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556531,"source":"dbSNP","strand":1,"feature_type":"variation","end":140556531,"alleles":["G","A","C"],"seq_region_name":"7","id":"rs1335152166","clinical_significance":[]},{"clinical_significance":[],"id":"rs1184592151","seq_region_name":"7","source":"dbSNP","start":140556534,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140556534,"feature_type":"variation","strand":1},{"alleles":["C","T"],"end":140556536,"feature_type":"variation","strand":1,"source":"dbSNP","start":140556536,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs912977455"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556538,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140556538,"seq_region_name":"7","id":"rs1404074373","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140556539,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556539,"clinical_significance":[],"id":"rs893706748","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556540,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140556540,"id":"rs1797370443","seq_region_name":"7","clinical_significance":[]},{"id":"rs751111027","seq_region_name":"7","clinical_significance":[],"end":140556541,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140556541,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556542,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140556542,"seq_region_name":"7","id":"rs1045575966","clinical_significance":[]},{"source":"dbSNP","start":140556545,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140556545,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs946758699"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585622976","source":"dbSNP","start":140556548,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140556548,"alleles":["C","T"],"feature_type":"variation","strand":1},{"id":"rs1797371022","seq_region_name":"7","clinical_significance":[],"start":140556552,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140556552,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797371132","source":"dbSNP","start":140556555,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140556555,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797371222","feature_type":"variation","strand":1,"end":140556556,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556556},{"feature_type":"variation","strand":1,"end":140556562,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556562,"clinical_significance":[],"seq_region_name":"7","id":"rs1166538199"},{"source":"dbSNP","start":140556566,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140556567,"alleles":["CT","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1474198326","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140556568,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556568,"clinical_significance":[],"seq_region_name":"7","id":"rs1797371517"},{"alleles":["A","G"],"end":140556579,"feature_type":"variation","strand":1,"source":"dbSNP","start":140556579,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs199572223"},{"id":"rs1472280179","seq_region_name":"7","clinical_significance":[],"start":140556580,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140556580,"alleles":["C","A","T"],"strand":1,"feature_type":"variation"},{"alleles":["T","C"],"end":140556582,"strand":1,"feature_type":"variation","start":140556582,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1042363662","clinical_significance":[]},{"seq_region_name":"7","id":"rs1462256463","clinical_significance":[],"start":140556584,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140556584,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"end":140556587,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140556587,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1797372093","seq_region_name":"7"},{"alleles":["C","T"],"end":140556589,"strand":1,"feature_type":"variation","start":140556589,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797372203","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797372309","clinical_significance":[],"strand":1,"feature_type":"variation","end":140556591,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556591,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1420210044","feature_type":"variation","strand":1,"end":140556602,"alleles":["AAA","AA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556600},{"seq_region_name":"7","id":"rs1456598406","clinical_significance":[],"end":140556606,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140556606,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797372636","alleles":["T","C"],"end":140556607,"feature_type":"variation","strand":1,"source":"dbSNP","start":140556607,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1162951035","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556608,"feature_type":"variation","strand":1,"end":140556608,"alleles":["A","G"]},{"end":140556609,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140556609,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs905665784","clinical_significance":[]},{"end":140556610,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140556610,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1396941955","seq_region_name":"7"},{"id":"rs1585623088","seq_region_name":"7","clinical_significance":[],"start":140556613,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140556613,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1411492556","clinical_significance":[],"end":140556622,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140556622,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797373363","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556629,"feature_type":"variation","strand":1,"end":140556629,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1338562243","clinical_significance":[],"start":140556630,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140556630,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs902490052","clinical_significance":[],"strand":1,"feature_type":"variation","end":140556631,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556631,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1797373657","clinical_significance":[],"end":140556632,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140556632,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs868814730","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140556633,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556633,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140556634,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556634,"source":"dbSNP","id":"rs573421905","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797373998","clinical_significance":[],"strand":1,"feature_type":"variation","end":140556640,"alleles":["ACCTCA","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556635,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556636,"feature_type":"variation","strand":1,"end":140556636,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130560425"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585623152","alleles":["C","T"],"end":140556637,"feature_type":"variation","strand":1,"source":"dbSNP","start":140556637,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140556639,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140556639,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs540708709","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556641,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140556641,"seq_region_name":"7","id":"rs1369898341","clinical_significance":[]},{"start":140556643,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140556643,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs899198527","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140556646,"alleles":["A","AGGCTGAGGTTAA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556646,"clinical_significance":[],"seq_region_name":"7","id":"rs1403122153"},{"start":140556646,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140556646,"strand":1,"feature_type":"variation","id":"rs1585623194","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1169001565","seq_region_name":"7","end":140556647,"alleles":["A","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140556647,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140556649,"alleles":["A","AA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556649,"source":"dbSNP","seq_region_name":"7","id":"rs1294599940","clinical_significance":[]},{"seq_region_name":"7","id":"rs994828663","clinical_significance":[],"alleles":["C","G","T"],"end":140556650,"strand":1,"feature_type":"variation","start":140556650,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556653,"source":"dbSNP","strand":1,"feature_type":"variation","end":140556653,"alleles":["T","C"],"id":"rs1163416221","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs535097603","clinical_significance":[],"alleles":["C","T"],"end":140556656,"strand":1,"feature_type":"variation","start":140556656,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1382803775","clinical_significance":[],"end":140556662,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140556662,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1797375498","clinical_significance":[],"alleles":["G","C"],"end":140556670,"strand":1,"feature_type":"variation","start":140556670,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1012395401","clinical_significance":[],"start":140556673,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140556673,"alleles":["C","A","T"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556676,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140556676,"clinical_significance":[],"seq_region_name":"7","id":"rs1797375742"},{"seq_region_name":"7","id":"rs1270476143","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556679,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AATTA","A"],"end":140556683},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556680,"feature_type":"variation","strand":1,"alleles":["ATTATTAT","ATTAT"],"end":140556687,"clinical_significance":[],"seq_region_name":"7","id":"rs761217947"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140556682,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556682,"source":"dbSNP","seq_region_name":"7","id":"rs1202425179","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140556686,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556686,"clinical_significance":[],"seq_region_name":"7","id":"rs886535650"},{"start":140556687,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140556687,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1009360081","clinical_significance":[]},{"id":"rs1017642769","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556691,"source":"dbSNP","strand":1,"feature_type":"variation","end":140556696,"alleles":["ACTTAC","AC"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556692,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140556692,"clinical_significance":[],"seq_region_name":"7","id":"rs1797376917"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140556694,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556694,"clinical_significance":[],"id":"rs1797377084","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1357582018","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556695,"source":"dbSNP","strand":1,"feature_type":"variation","end":140556695,"alleles":["A","G"]},{"alleles":["C","A"],"end":140556696,"strand":1,"feature_type":"variation","start":140556696,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130560632","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1314418426","feature_type":"variation","strand":1,"end":140556697,"alleles":["CC","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556696},{"seq_region_name":"7","id":"rs1797377538","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140556697,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556697,"source":"dbSNP"},{"id":"rs1240921511","seq_region_name":"7","clinical_significance":[],"start":140556702,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140556702,"strand":1,"feature_type":"variation"},{"alleles":["C","G"],"end":140556703,"feature_type":"variation","strand":1,"source":"dbSNP","start":140556703,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797377863"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556704,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140556704,"clinical_significance":[],"seq_region_name":"7","id":"rs1797378052"},{"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140556705,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556705,"source":"dbSNP","id":"rs577277444","seq_region_name":"7","clinical_significance":[]},{"id":"rs1797378387","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140556708,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556708,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556709,"source":"dbSNP","strand":1,"feature_type":"variation","end":140556710,"alleles":["TC","-"],"seq_region_name":"7","id":"rs1797378556","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140556710,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556710,"clinical_significance":[],"id":"rs1797378741","seq_region_name":"7"},{"id":"rs962982805","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140556711,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556711,"source":"dbSNP"},{"seq_region_name":"7","id":"rs141120790","clinical_significance":[],"start":140556714,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140556714,"alleles":["G","A","C"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556715,"feature_type":"variation","strand":1,"end":140556715,"alleles":["C","T"],"clinical_significance":[],"id":"rs1019145287","seq_region_name":"7"},{"alleles":["T","C"],"end":140556716,"strand":1,"feature_type":"variation","start":140556716,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs781755021","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1259691119","clinical_significance":[],"alleles":["T","G"],"end":140556717,"strand":1,"feature_type":"variation","start":140556717,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140556728,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140556732,"alleles":["TGATT","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1422206538"},{"seq_region_name":"7","id":"rs964845415","clinical_significance":[],"start":140556731,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140556731,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556732,"source":"dbSNP","strand":1,"feature_type":"variation","end":140556732,"alleles":["T","G"],"seq_region_name":"7","id":"rs1025986892","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1187068675","source":"dbSNP","start":140556735,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140556735,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556738,"source":"dbSNP","strand":1,"feature_type":"variation","end":140556743,"alleles":["AAAAAA","AAAAA"],"seq_region_name":"7","id":"rs1373904287","clinical_significance":[]},{"end":140556741,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140556741,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1036795895","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140556745,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140556745,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1166516945"},{"feature_type":"variation","strand":1,"end":140556748,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556748,"clinical_significance":[],"seq_region_name":"7","id":"rs563149149"},{"id":"rs1363299936","seq_region_name":"7","clinical_significance":[],"start":140556749,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140556749,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs950339667","source":"dbSNP","start":140556753,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140556753,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140556756,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556756,"source":"dbSNP","seq_region_name":"7","id":"rs77772798","clinical_significance":[]},{"clinical_significance":[],"id":"rs1409609980","seq_region_name":"7","end":140556758,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140556758,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556761,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140556761,"clinical_significance":[],"id":"rs1797381085","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556762,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140556762,"clinical_significance":[],"seq_region_name":"7","id":"rs1797381189"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1175342286","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140556764,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556764},{"seq_region_name":"7","id":"rs1469575414","clinical_significance":[],"strand":1,"feature_type":"variation","end":140556765,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556765,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs957066860","source":"dbSNP","start":140556771,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140556771,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1247017335","clinical_significance":[],"end":140556772,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140556772,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140556775,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140556775,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1563138648"},{"source":"dbSNP","start":140556777,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140556777,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1314724604"},{"alleles":["T","C"],"end":140556778,"feature_type":"variation","strand":1,"source":"dbSNP","start":140556778,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs988485933","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs912855138","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556784,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140556784},{"seq_region_name":"7","id":"rs1291286781","clinical_significance":[],"start":140556786,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140556786,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140556787,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556787,"clinical_significance":[],"seq_region_name":"7","id":"rs1797382173"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797382274","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556801,"feature_type":"variation","strand":1,"end":140556801,"alleles":["C","A"]},{"strand":1,"feature_type":"variation","end":140556804,"alleles":["A","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556804,"source":"dbSNP","seq_region_name":"7","id":"rs7804236","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556806,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140556806,"seq_region_name":"7","id":"rs1318804145","clinical_significance":[]},{"end":140556814,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140556814,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1318539014"},{"clinical_significance":[],"id":"rs1223674015","seq_region_name":"7","source":"dbSNP","start":140556816,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140556816,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556818,"source":"dbSNP","strand":1,"feature_type":"variation","end":140556818,"alleles":["A","C","G"],"id":"rs1585623602","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797382869","clinical_significance":[],"start":140556819,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140556819,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1327864766","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140556820,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556820},{"id":"rs1368957392","seq_region_name":"7","clinical_significance":[],"start":140556825,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140556825,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556826,"source":"dbSNP","strand":1,"feature_type":"variation","end":140556826,"alleles":["C","T"],"seq_region_name":"7","id":"rs1285799833","clinical_significance":[]},{"seq_region_name":"7","id":"rs1403471437","clinical_significance":[],"strand":1,"feature_type":"variation","end":140556829,"alleles":["A","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556829,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556831,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140556831,"clinical_significance":[],"seq_region_name":"7","id":"rs2130561016"},{"strand":1,"feature_type":"variation","end":140556832,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556832,"source":"dbSNP","id":"rs1230991601","seq_region_name":"7","clinical_significance":[]},{"end":140556833,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140556833,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797383356","clinical_significance":[]},{"end":140556839,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140556839,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1345341777"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556841,"feature_type":"variation","strand":1,"alleles":["T","A","G"],"end":140556841,"clinical_significance":[],"seq_region_name":"7","id":"rs1302142860"},{"seq_region_name":"7","id":"rs1295882244","clinical_significance":[],"start":140556845,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140556845,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1346395738","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556846,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140556846},{"id":"rs1156343603","seq_region_name":"7","clinical_significance":[],"alleles":["A","G"],"end":140556847,"strand":1,"feature_type":"variation","start":140556847,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1797384014","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140556849,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556849,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1281745899","clinical_significance":[],"alleles":["C","T"],"end":140556851,"strand":1,"feature_type":"variation","start":140556851,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556858,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140556858,"clinical_significance":[],"id":"rs181482920","seq_region_name":"7"},{"start":140556871,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C","T"],"end":140556871,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs915178888","clinical_significance":[]},{"end":140556874,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140556874,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797384551"},{"clinical_significance":[],"seq_region_name":"7","id":"rs117112744","feature_type":"variation","strand":1,"end":140556877,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556877},{"feature_type":"variation","strand":1,"end":140556881,"alleles":["AAAA","AAAAA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556878,"clinical_significance":[],"seq_region_name":"7","id":"rs1585623709"},{"clinical_significance":[],"id":"rs1479324570","seq_region_name":"7","alleles":["A","C"],"end":140556879,"feature_type":"variation","strand":1,"source":"dbSNP","start":140556879,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556880,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140556880,"seq_region_name":"7","id":"rs1482304763","clinical_significance":[]},{"source":"dbSNP","start":140556881,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140556881,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1797385100","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797385196","alleles":["A","G"],"end":140556884,"feature_type":"variation","strand":1,"source":"dbSNP","start":140556884,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1797385307","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140556887,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556887,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556888,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140556888,"clinical_significance":[],"seq_region_name":"7","id":"rs1585623734"},{"clinical_significance":[],"seq_region_name":"7","id":"rs546271863","end":140556889,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140556889,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1199965838","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140556891,"strand":1,"feature_type":"variation","start":140556891,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["A","G"],"end":140556892,"strand":1,"feature_type":"variation","start":140556892,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs570924824","clinical_significance":[]},{"end":140556898,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140556898,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130561223","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs749615734","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556901,"feature_type":"variation","strand":1,"end":140556901,"alleles":["T","C"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556905,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140556905,"clinical_significance":[],"id":"rs937160328","seq_region_name":"7"},{"start":140556912,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140556912,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1038272758","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797386262","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140556914,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556914,"source":"dbSNP"},{"source":"dbSNP","start":140556915,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140556915,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1259000855"},{"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140556916,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556916,"source":"dbSNP","seq_region_name":"7","id":"rs1797386611","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797386746","end":140556924,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140556924,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1797386958","clinical_significance":[],"start":140556926,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140556926,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"end":140556928,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140556928,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1797387118","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1215123392","end":140556932,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140556932,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1797387419","clinical_significance":[],"strand":1,"feature_type":"variation","end":140556933,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556933,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140556948,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556948,"clinical_significance":[],"seq_region_name":"7","id":"rs1797387525"},{"alleles":["A","G"],"end":140556949,"strand":1,"feature_type":"variation","start":140556949,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs2130561316","seq_region_name":"7","clinical_significance":[]},{"end":140556950,"alleles":["T","C","G"],"strand":1,"feature_type":"variation","start":140556950,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1312899886","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140556959,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556959,"source":"dbSNP","seq_region_name":"7","id":"rs1797387783","clinical_significance":[]},{"alleles":["C","T"],"end":140556962,"feature_type":"variation","strand":1,"source":"dbSNP","start":140556962,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs919837311"},{"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140556964,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556964,"source":"dbSNP","seq_region_name":"7","id":"rs532087387","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs73491552","feature_type":"variation","strand":1,"end":140556966,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556966},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140556968,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556968,"clinical_significance":[],"seq_region_name":"7","id":"rs1047727948"},{"clinical_significance":[],"seq_region_name":"7","id":"rs886418639","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556969,"feature_type":"variation","strand":1,"end":140556969,"alleles":["G","C"]},{"start":140556975,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TTT","TTTT"],"end":140556977,"strand":1,"feature_type":"variation","id":"rs1797388409","seq_region_name":"7","clinical_significance":[]},{"id":"rs1008997599","seq_region_name":"7","clinical_significance":[],"start":140556978,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C","T"],"end":140556978,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140556979,"feature_type":"variation","strand":1,"end":140556979,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1797388676"},{"source":"dbSNP","start":140556980,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140556980,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1797388791","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556981,"source":"dbSNP","strand":1,"feature_type":"variation","end":140556981,"alleles":["T","C"],"id":"rs939340180","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","T"],"end":140556985,"strand":1,"feature_type":"variation","start":140556985,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1454599101","clinical_significance":[]},{"id":"rs1797389091","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140556990,"alleles":["CC","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556989,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1175399599","seq_region_name":"7","alleles":["C","A"],"end":140556998,"feature_type":"variation","strand":1,"source":"dbSNP","start":140556998,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140556999,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140556999,"id":"rs1797389296","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557000,"source":"dbSNP","strand":1,"feature_type":"variation","end":140557000,"alleles":["A","G"],"seq_region_name":"7","id":"rs1286797353","clinical_significance":[]},{"end":140557010,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140557010,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1056972263"},{"strand":1,"feature_type":"variation","alleles":["TCTCTCT","TCT"],"end":140557017,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557011,"source":"dbSNP","seq_region_name":"7","id":"rs1250290266","clinical_significance":[]},{"alleles":["C","T"],"end":140557014,"feature_type":"variation","strand":1,"source":"dbSNP","start":140557014,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs752346244","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1468169371","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["AA","-"],"end":140557019,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557018},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557021,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140557021,"clinical_significance":[],"id":"rs1797389993","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1012862589","clinical_significance":[],"strand":1,"feature_type":"variation","end":140557023,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557023,"source":"dbSNP"},{"start":140557029,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140557029,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs376844394","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797390285","clinical_significance":[],"alleles":["T","C"],"end":140557035,"strand":1,"feature_type":"variation","start":140557035,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["G","T"],"end":140557038,"feature_type":"variation","strand":1,"source":"dbSNP","start":140557038,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1430129482"},{"seq_region_name":"7","id":"rs1259890391","clinical_significance":[],"start":140557041,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140557041,"alleles":["T","A","C","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1186208964","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557046,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140557046},{"seq_region_name":"7","id":"rs1797390670","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557047,"source":"dbSNP","strand":1,"feature_type":"variation","end":140557047,"alleles":["A","C"]},{"start":140557049,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140557049,"alleles":["T","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797390761","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140557051,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557051,"source":"dbSNP","id":"rs1483617860","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1158650115","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557052,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140557052},{"clinical_significance":[],"seq_region_name":"7","id":"rs554899990","feature_type":"variation","strand":1,"alleles":["AAAAAAAAAAA","AAAAAAAAA","AAAAAAAAAA","AAAAAAAAAAAA"],"end":140557062,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557052},{"strand":1,"feature_type":"variation","end":140557054,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557054,"source":"dbSNP","seq_region_name":"7","id":"rs1797391241","clinical_significance":[]},{"start":140557058,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140557058,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797391336","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs996345124","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557063,"feature_type":"variation","strand":1,"end":140557063,"alleles":["T","A"]},{"id":"rs745928939","seq_region_name":"7","clinical_significance":[],"start":140557065,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140557065,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140557066,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140557066,"alleles":["G","A","C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs144945934"},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140557070,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557070,"source":"dbSNP","seq_region_name":"7","id":"rs1213692858","clinical_significance":[]},{"id":"rs1797391851","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557071,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140557071},{"source":"dbSNP","start":140557073,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140557073,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1025872285","seq_region_name":"7"},{"alleles":["G","A","C"],"end":140557075,"feature_type":"variation","strand":1,"source":"dbSNP","start":140557075,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs950393172"},{"source":"dbSNP","start":140557078,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140557078,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797392236"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557081,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140557081,"clinical_significance":[],"seq_region_name":"7","id":"rs1797392340"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1008549251","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557082,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140557082},{"start":140557084,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140557084,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1405231342","clinical_significance":[]},{"seq_region_name":"7","id":"rs1010865886","clinical_significance":[],"strand":1,"feature_type":"variation","end":140557088,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557088,"source":"dbSNP"},{"start":140557089,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140557089,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs185971417","clinical_significance":[]},{"alleles":["T","C"],"end":140557090,"strand":1,"feature_type":"variation","start":140557090,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1371196725","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130561701","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557096,"source":"dbSNP","strand":1,"feature_type":"variation","end":140557096,"alleles":["A","C"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557107,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140557107,"seq_region_name":"7","id":"rs1169926012","clinical_significance":[]},{"end":140557109,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140557109,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs554777384","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140557112,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557112,"source":"dbSNP","seq_region_name":"7","id":"rs1797393193","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557116,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140557116,"clinical_significance":[],"seq_region_name":"7","id":"rs1303991289"},{"seq_region_name":"7","id":"rs974866954","clinical_significance":[],"alleles":["T","C"],"end":140557119,"strand":1,"feature_type":"variation","start":140557119,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557126,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140557126,"clinical_significance":[],"seq_region_name":"7","id":"rs1797393493"},{"strand":1,"feature_type":"variation","end":140557130,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557130,"source":"dbSNP","seq_region_name":"7","id":"rs1178579485","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs191669528","source":"dbSNP","start":140557132,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140557132,"feature_type":"variation","strand":1},{"start":140557133,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140557133,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs971439970","clinical_significance":[]},{"seq_region_name":"7","id":"rs1460958112","clinical_significance":[],"start":140557142,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140557142,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557147,"source":"dbSNP","strand":1,"feature_type":"variation","end":140557147,"alleles":["G","A"],"id":"rs1232537952","seq_region_name":"7","clinical_significance":[]},{"start":140557154,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140557154,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1198138207","clinical_significance":[]},{"start":140557156,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140557156,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs981183761","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557158,"feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140557158,"clinical_significance":[],"id":"rs1797394438","seq_region_name":"7"},{"seq_region_name":"7","id":"rs927025891","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140557161,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557161,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797394675","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557167,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140557167},{"alleles":["C","T"],"end":140557170,"strand":1,"feature_type":"variation","start":140557170,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs958569670","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1226162689","end":140557171,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140557171,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1797394966","clinical_significance":[],"start":140557175,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140557175,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1359755427","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["GGG","GG"],"end":140557178,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557176,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1797395330","seq_region_name":"7","end":140557177,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140557177,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585624269","feature_type":"variation","strand":1,"end":140557178,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557178},{"alleles":["G","A","T"],"end":140557180,"feature_type":"variation","strand":1,"source":"dbSNP","start":140557180,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs973886435"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557186,"source":"dbSNP","strand":1,"feature_type":"variation","end":140557186,"alleles":["C","CC"],"seq_region_name":"7","id":"rs35820663","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140557189,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557189,"source":"dbSNP","seq_region_name":"7","id":"rs1797395813","clinical_significance":[]},{"source":"dbSNP","start":140557190,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140557190,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797395979"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557191,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140557191,"clinical_significance":[],"seq_region_name":"7","id":"rs1797396138"},{"clinical_significance":[],"seq_region_name":"7","id":"rs919723163","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557192,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140557192},{"source":"dbSNP","start":140557193,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140557193,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797396410"},{"start":140557198,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140557198,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1423000983","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs977994938","feature_type":"variation","strand":1,"end":140557199,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557199},{"seq_region_name":"7","id":"rs923839801","clinical_significance":[],"strand":1,"feature_type":"variation","end":140557202,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557202,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1261398406","clinical_significance":[],"strand":1,"feature_type":"variation","end":140557203,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557203,"source":"dbSNP"},{"start":140557206,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140557206,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs929930479","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1393993415","source":"dbSNP","start":140557207,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140557207,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557208,"feature_type":"variation","strand":1,"end":140557208,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs939392357"},{"source":"dbSNP","start":140557213,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140557213,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1425492594"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1056459406","source":"dbSNP","start":140557218,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140557218,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140557222,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557222,"clinical_significance":[],"seq_region_name":"7","id":"rs200998585"},{"source":"dbSNP","start":140557225,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140557225,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1047395559"},{"end":140557229,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140557229,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1797397653","seq_region_name":"7"},{"source":"dbSNP","start":140557230,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140557230,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797397768"},{"seq_region_name":"7","id":"rs534304767","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140557231,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557231,"source":"dbSNP"},{"id":"rs1797398005","seq_region_name":"7","clinical_significance":[],"start":140557232,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140557232,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557234,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C","T"],"end":140557234,"id":"rs535784704","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140557235,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140557235,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs916533391"},{"clinical_significance":[],"seq_region_name":"7","id":"rs143794727","end":140557242,"alleles":["ACA","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140557240,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140557241,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557241,"source":"dbSNP","seq_region_name":"7","id":"rs73491556","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797398740","clinical_significance":[],"start":140557243,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140557243,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557244,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140557244,"seq_region_name":"7","id":"rs187217988","clinical_significance":[]},{"alleles":["T","C"],"end":140557248,"feature_type":"variation","strand":1,"source":"dbSNP","start":140557248,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1192725095","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557250,"source":"dbSNP","strand":1,"feature_type":"variation","end":140557250,"alleles":["A","T"],"seq_region_name":"7","id":"rs898677838","clinical_significance":[]},{"clinical_significance":[],"id":"rs1293477561","seq_region_name":"7","source":"dbSNP","start":140557255,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140557255,"feature_type":"variation","strand":1},{"start":140557257,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140557257,"alleles":["T","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797399301","clinical_significance":[]},{"seq_region_name":"7","id":"rs994323357","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140557263,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557263,"source":"dbSNP"},{"source":"dbSNP","start":140557267,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140557267,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1047368565"},{"id":"rs544552381","seq_region_name":"7","clinical_significance":[],"start":140557269,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140557269,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs11977342","source":"dbSNP","start":140557270,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140557270,"alleles":["T","G"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557275,"source":"dbSNP","strand":1,"feature_type":"variation","end":140557275,"alleles":["C","T"],"seq_region_name":"7","id":"rs1797399855","clinical_significance":[]},{"end":140557276,"alleles":["A","G","T"],"strand":1,"feature_type":"variation","start":140557276,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1432541059","clinical_significance":[]},{"seq_region_name":"7","id":"rs1040522071","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557277,"source":"dbSNP","strand":1,"feature_type":"variation","end":140557277,"alleles":["T","C"]},{"clinical_significance":[],"id":"rs2130562207","seq_region_name":"7","feature_type":"variation","strand":1,"end":140557278,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557278},{"start":140557279,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140557279,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1306250919","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797400301","clinical_significance":[],"start":140557285,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140557285,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs556274419","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557292,"feature_type":"variation","strand":1,"end":140557292,"alleles":["C","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557297,"source":"dbSNP","strand":1,"feature_type":"variation","end":140557297,"alleles":["C","T"],"seq_region_name":"7","id":"rs932018682","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140557298,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557298,"clinical_significance":[],"seq_region_name":"7","id":"rs1301517051"},{"seq_region_name":"7","id":"rs1009014996","clinical_significance":[],"strand":1,"feature_type":"variation","end":140557299,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557299,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557301,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140557301,"seq_region_name":"7","id":"rs1585624658","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557302,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140557302,"seq_region_name":"7","id":"rs1797400946","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1054630116","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557303,"feature_type":"variation","strand":1,"end":140557303,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs893271008","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140557306,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557306},{"seq_region_name":"7","id":"rs1797401255","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557307,"source":"dbSNP","strand":1,"feature_type":"variation","end":140557307,"alleles":["A","G"]},{"end":140557309,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140557309,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1010501475","clinical_significance":[]},{"seq_region_name":"7","id":"rs1160389817","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140557310,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557310,"source":"dbSNP"},{"id":"rs1451776443","seq_region_name":"7","clinical_significance":[],"start":140557321,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140557321,"strand":1,"feature_type":"variation"},{"end":140557328,"alleles":["T","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140557328,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1363707443"},{"id":"rs1020940146","seq_region_name":"7","clinical_significance":[],"start":140557331,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140557331,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563138991","source":"dbSNP","start":140557337,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140557337,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1481623283","clinical_significance":[],"end":140557338,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140557338,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1797402009","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557345,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140557345},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557347,"feature_type":"variation","strand":1,"end":140557347,"alleles":["G","A"],"clinical_significance":[],"id":"rs1585624771","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1797402217","clinical_significance":[],"strand":1,"feature_type":"variation","end":140557349,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557349,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140557352,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557352,"clinical_significance":[],"id":"rs1267221161","seq_region_name":"7"},{"end":140557354,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140557354,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs79420594","clinical_significance":[]},{"source":"dbSNP","start":140557356,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140557356,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797402580"},{"strand":1,"feature_type":"variation","end":140557359,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557359,"source":"dbSNP","seq_region_name":"7","id":"rs1797402698","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140557362,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557362,"clinical_significance":[],"seq_region_name":"7","id":"rs1797402811"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557369,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140557369,"id":"rs1196763482","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","T"],"end":140557374,"strand":1,"feature_type":"variation","start":140557374,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1450709253","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557378,"source":"dbSNP","strand":1,"feature_type":"variation","end":140557378,"alleles":["G","C"],"seq_region_name":"7","id":"rs1284302671","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557381,"feature_type":"variation","strand":1,"end":140557381,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1797403249"},{"seq_region_name":"7","id":"rs964693024","clinical_significance":[],"alleles":["C","T"],"end":140557382,"strand":1,"feature_type":"variation","start":140557382,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs906889633","seq_region_name":"7","alleles":["G","T"],"end":140557386,"feature_type":"variation","strand":1,"source":"dbSNP","start":140557386,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797403359","source":"dbSNP","start":140557392,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140557392,"feature_type":"variation","strand":1},{"alleles":["C","G"],"end":140557393,"feature_type":"variation","strand":1,"source":"dbSNP","start":140557393,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs575124179","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1224117540","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557395,"feature_type":"variation","strand":1,"end":140557395,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797403697","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557396,"feature_type":"variation","strand":1,"end":140557396,"alleles":["G","A"]},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140557401,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557401,"clinical_significance":[],"seq_region_name":"7","id":"rs1797403810"},{"alleles":["A","C"],"end":140557402,"strand":1,"feature_type":"variation","start":140557402,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1325331360","seq_region_name":"7","clinical_significance":[]},{"start":140557411,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140557414,"alleles":["AAAA","AAA"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1394791445","clinical_significance":[]},{"source":"dbSNP","start":140557413,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140557413,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1462257072"},{"start":140557415,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140557415,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1295656926","clinical_significance":[]},{"id":"rs1797404380","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140557418,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557418,"source":"dbSNP"},{"start":140557419,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140557419,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797404471","clinical_significance":[]},{"alleles":["T","C"],"end":140557420,"strand":1,"feature_type":"variation","start":140557420,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130562570","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557421,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140557421,"clinical_significance":[],"seq_region_name":"7","id":"rs1002490060"},{"alleles":["C","-"],"end":140557426,"strand":1,"feature_type":"variation","start":140557426,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1380592833","clinical_significance":[]},{"seq_region_name":"7","id":"rs1384436435","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557428,"source":"dbSNP","strand":1,"feature_type":"variation","end":140557428,"alleles":["G","C"]},{"clinical_significance":[],"id":"rs1177703563","seq_region_name":"7","feature_type":"variation","strand":1,"end":140557434,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557434},{"clinical_significance":[],"seq_region_name":"7","id":"rs542134933","source":"dbSNP","start":140557436,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140557436,"alleles":["C","T"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140557437,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140557437,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1427583160"},{"id":"rs1797405153","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557438,"source":"dbSNP","strand":1,"feature_type":"variation","end":140557438,"alleles":["G","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1176201308","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140557440,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557440},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797405349","source":"dbSNP","start":140557444,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","G"],"end":140557444,"feature_type":"variation","strand":1},{"start":140557447,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140557447,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585625054","clinical_significance":[]},{"source":"dbSNP","start":140557453,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","G"],"end":140557453,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1475968201","seq_region_name":"7"},{"alleles":["A","G"],"end":140557455,"feature_type":"variation","strand":1,"source":"dbSNP","start":140557455,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs995960162"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797405863","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557462,"feature_type":"variation","strand":1,"end":140557462,"alleles":["T","C"]},{"end":140557465,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140557465,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1308420126","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140557468,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557468,"source":"dbSNP","seq_region_name":"7","id":"rs1194956244","clinical_significance":[]},{"start":140557472,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140557472,"alleles":["C","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797406182","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557480,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140557480,"seq_region_name":"7","id":"rs1444774885","clinical_significance":[]},{"alleles":["C","A","T"],"end":140557482,"strand":1,"feature_type":"variation","start":140557482,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1246883975","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1462613309","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557485,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140557485},{"clinical_significance":[],"seq_region_name":"7","id":"rs112157654","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557486,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140557486},{"id":"rs1204152164","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["TTTTTTT","TTTT","TTTTTTTT"],"end":140557492,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557486,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557492,"source":"dbSNP","strand":1,"feature_type":"variation","end":140557492,"alleles":["T","A"],"seq_region_name":"7","id":"rs1222654146","clinical_significance":[]},{"seq_region_name":"7","id":"rs1339903342","clinical_significance":[],"start":140557496,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140557496,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs138835234","seq_region_name":"7","end":140557499,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140557499,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797407399","alleles":["T","C"],"end":140557500,"feature_type":"variation","strand":1,"source":"dbSNP","start":140557500,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140557501,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C","T"],"end":140557501,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1484929718","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1225529820","clinical_significance":[],"start":140557502,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TTTTTT","TTTTTTT"],"end":140557507,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557505,"source":"dbSNP","strand":1,"feature_type":"variation","end":140557505,"alleles":["T","G"],"seq_region_name":"7","id":"rs1337497032","clinical_significance":[]},{"alleles":["TTAGT","T"],"end":140557510,"strand":1,"feature_type":"variation","start":140557506,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797408100","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797408222","clinical_significance":[],"alleles":["-","ATATATA"],"end":140557506,"strand":1,"feature_type":"variation","start":140557507,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1797408322","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557507,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140557507},{"seq_region_name":"7","id":"rs1797408425","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557507,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TAGTATATA","TA"],"end":140557515},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130562824","feature_type":"variation","strand":1,"end":140557508,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557508},{"end":140557508,"alleles":["-","ATAT","TT"],"strand":1,"feature_type":"variation","start":140557509,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1563139096","clinical_significance":[]},{"start":140557509,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140557509,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1404501945","clinical_significance":[]},{"alleles":["G","-"],"end":140557509,"strand":1,"feature_type":"variation","start":140557509,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1455014984","clinical_significance":[]},{"end":140557510,"alleles":["GT","GTGT"],"strand":1,"feature_type":"variation","start":140557509,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797408901","clinical_significance":[]},{"end":140557512,"alleles":["GTAT","GTATGTAT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140557509,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1563139115","seq_region_name":"7"},{"alleles":["-","ATAT"],"end":140557509,"strand":1,"feature_type":"variation","start":140557510,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1554467280","clinical_significance":[]},{"seq_region_name":"7","id":"rs1554467279","clinical_significance":[],"alleles":["T","TGTAT","TGTATAT","TGTATATATAT","TGTATATATATAT","TGTATATATATATAT","TGTATATATATATATAT","TGTATATATATATATATATAT"],"end":140557510,"strand":1,"feature_type":"variation","start":140557510,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["TAT","TATGTATATAT"],"end":140557512,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557510,"source":"dbSNP","id":"rs1797409891","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797410077","source":"dbSNP","start":140557510,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140557513,"alleles":["TATA","TATACATATATATATA"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1554467281","feature_type":"variation","strand":1,"alleles":["TATATATATA","TATATATATACATATATATATATATATA"],"end":140557519,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557510},{"clinical_significance":[],"seq_region_name":"7","id":"rs1264932411","source":"dbSNP","start":140557510,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TATATATATATATATATATATAT","TATATATATATATAT","TATATATATATATATAT","TATATATATATATATATAT","TATATATATATATATATATAT","TATATATATATATATATATATATAT","TATATATATATATATATATATATATAT","TATATATATATATATATATATATATATAT","TATATATATATATATATATATATATATATAT","TATATATATATATATATATATATATATATATAT","TATATATATATATATATATATATATATATATATAT","TATATATATATATATATATATATATATATATATATAT","TATATATATATATATATATATATATATATATATATATAT","TATATATATATATATATATATATATATATATATATATATAT","TATATATATATATATATATATATATATATATATATATATATAT","TATATATATATATATATATATATATATATATATATATATATATATAT"],"end":140557532,"feature_type":"variation","strand":1},{"id":"rs796321879","seq_region_name":"7","clinical_significance":[],"end":140557511,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140557511,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1267686044","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140557512,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557512},{"id":"rs1797411653","seq_region_name":"7","clinical_significance":[],"start":140557512,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","TTT"],"end":140557512,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1316045084","alleles":["T","C"],"end":140557514,"feature_type":"variation","strand":1,"source":"dbSNP","start":140557514,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563139157","source":"dbSNP","start":140557514,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140557514,"alleles":["T","TTT"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1248234384","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557515,"feature_type":"variation","strand":1,"alleles":["ATA","ATACATA"],"end":140557517},{"alleles":["T","TTT"],"end":140557516,"strand":1,"feature_type":"variation","start":140557516,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1563139168","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797412132","clinical_significance":[],"alleles":["T","C"],"end":140557516,"strand":1,"feature_type":"variation","start":140557516,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1797412336","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557517,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","ACA"],"end":140557517},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557517,"feature_type":"variation","strand":1,"alleles":["A","-"],"end":140557517,"clinical_significance":[],"seq_region_name":"7","id":"rs1797412428"},{"feature_type":"variation","strand":1,"end":140557529,"alleles":["ATATATATATATA","ATATATATATATAAATATATATATATA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557517,"clinical_significance":[],"seq_region_name":"7","id":"rs1797412552"},{"alleles":["ATATATATATATATA","-"],"end":140557531,"feature_type":"variation","strand":1,"source":"dbSNP","start":140557517,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1380747043"},{"end":140557520,"alleles":["TAT","TATGTAT"],"strand":1,"feature_type":"variation","start":140557518,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797412792","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797412992","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557518,"feature_type":"variation","strand":1,"end":140557530,"alleles":["TATATATATATAT","TATATATATATATGTATATATATATAT"]},{"end":140557532,"alleles":["TATATATATATATAT","TATATATATATATATATATATATATTTATATATATATATAT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140557518,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130563077"},{"start":140557519,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140557527,"alleles":["ATATATATA","-"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797413158","clinical_significance":[]},{"end":140557531,"alleles":["ATATATATATATA","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140557519,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797413300"},{"end":140557520,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140557520,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1443567806"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1314960650","source":"dbSNP","start":140557520,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TATATATATATATTT","T"],"end":140557534,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1797413623","seq_region_name":"7","alleles":["ATA","ATACATA"],"end":140557523,"feature_type":"variation","strand":1,"source":"dbSNP","start":140557521,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557521,"source":"dbSNP","strand":1,"feature_type":"variation","end":140557527,"alleles":["ATATATA","-"],"id":"rs1563139185","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797413879","clinical_significance":[],"start":140557521,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140557529,"alleles":["ATATATATA","-"],"strand":1,"feature_type":"variation"},{"id":"rs1356578579","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557521,"source":"dbSNP","strand":1,"feature_type":"variation","end":140557531,"alleles":["ATATATATATA","-"]},{"feature_type":"variation","strand":1,"end":140557533,"alleles":["TATATATATATT","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557522,"clinical_significance":[],"id":"rs1563139195","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1327290375","clinical_significance":[],"start":140557522,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TATATATATATTT","T"],"end":140557534,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1407815159","source":"dbSNP","start":140557522,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140557537,"alleles":["TATATATATATTTTTT","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1369518559","feature_type":"variation","strand":1,"end":140557538,"alleles":["TATATATATATTTTTTT","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557522},{"start":140557522,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140557542,"alleles":["TATATATATATTTTTTTTTTT","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1335736247","clinical_significance":[]},{"seq_region_name":"7","id":"rs1563139207","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557523,"source":"dbSNP","strand":1,"feature_type":"variation","end":140557523,"alleles":["A","-"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585625506","feature_type":"variation","strand":1,"end":140557523,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557523},{"id":"rs1797414808","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140557523,"alleles":["A","ACA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557523,"source":"dbSNP"},{"start":140557523,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140557527,"alleles":["ATATA","-"],"strand":1,"feature_type":"variation","id":"rs1563139209","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1445922309","source":"dbSNP","start":140557523,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["ATATATA","-"],"end":140557529,"feature_type":"variation","strand":1},{"end":140557531,"alleles":["ATATATATA","-"],"strand":1,"feature_type":"variation","start":140557523,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1382863857","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797415383","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557523,"feature_type":"variation","strand":1,"end":140557532,"alleles":["ATATATATAT","ATATATATATATACATATATATAT"]},{"clinical_significance":[],"id":"rs1797415493","seq_region_name":"7","alleles":["TATATATATTTTT","T"],"end":140557536,"feature_type":"variation","strand":1,"source":"dbSNP","start":140557524,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140557525,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140557525,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs867821270","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557525,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","-"],"end":140557525,"seq_region_name":"7","id":"rs1797415710","clinical_significance":[]},{"alleles":["ATA","-"],"end":140557527,"strand":1,"feature_type":"variation","start":140557525,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1563139224","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797415815","feature_type":"variation","strand":1,"end":140557527,"alleles":["ATA","ATACATA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557525},{"clinical_significance":[],"seq_region_name":"7","id":"rs1181158016","source":"dbSNP","start":140557525,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["ATATA","-"],"end":140557529,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1470484910","source":"dbSNP","start":140557525,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["ATATATA","-"],"end":140557531,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140557533,"alleles":["TATATATT","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557526,"clinical_significance":[],"seq_region_name":"7","id":"rs1179359855"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557526,"feature_type":"variation","strand":1,"end":140557534,"alleles":["TATATATTT","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1797416372"},{"seq_region_name":"7","id":"rs1797416491","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["TATATATTTT","T"],"end":140557535,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557526,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557526,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TATATATTTTTTT","T"],"end":140557538,"seq_region_name":"7","id":"rs1482635602","clinical_significance":[]},{"id":"rs1797416711","seq_region_name":"7","clinical_significance":[],"alleles":["TATATATTTTTTTT","T"],"end":140557539,"strand":1,"feature_type":"variation","start":140557526,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1324708947","clinical_significance":[],"alleles":["TATATATTTTTTTTT","T"],"end":140557540,"strand":1,"feature_type":"variation","start":140557526,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs868392045","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557527,"feature_type":"variation","strand":1,"end":140557527,"alleles":["A","G","T"]},{"source":"dbSNP","start":140557527,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140557527,"alleles":["A","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1563139237"},{"id":"rs1292760229","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140557529,"alleles":["ATA","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557527,"source":"dbSNP"},{"alleles":["ATATA","-"],"end":140557531,"feature_type":"variation","strand":1,"source":"dbSNP","start":140557527,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1225084932"},{"clinical_significance":[],"id":"rs1563139259","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557528,"feature_type":"variation","strand":1,"alleles":["T","TT","TTTT"],"end":140557528},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557528,"feature_type":"variation","strand":1,"end":140557533,"alleles":["TATATT","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1797417567"},{"feature_type":"variation","strand":1,"alleles":["TATATTT","T"],"end":140557534,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557528,"clinical_significance":[],"id":"rs1797417675","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1289259182","feature_type":"variation","strand":1,"alleles":["TATATTTTT","T"],"end":140557536,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557528},{"seq_region_name":"7","id":"rs1797417886","clinical_significance":[],"strand":1,"feature_type":"variation","end":140557537,"alleles":["TATATTTTTT","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557528,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1224775772","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557528,"feature_type":"variation","strand":1,"alleles":["TATATTTTTTT","T"],"end":140557538},{"source":"dbSNP","start":140557528,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TATATTTTTTTT","T"],"end":140557539,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1376200078","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1278333611","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557528,"feature_type":"variation","strand":1,"end":140557540,"alleles":["TATATTTTTTTTT","T"]},{"id":"rs1409573473","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["TATATTTTTTTTTT","T"],"end":140557541,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557528,"source":"dbSNP"},{"id":"rs1346616848","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140557543,"alleles":["TATATTTTTTTTTTTT","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557528,"source":"dbSNP"},{"clinical_significance":[],"id":"rs867173820","seq_region_name":"7","end":140557529,"alleles":["A","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140557529,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["A","-"],"end":140557529,"feature_type":"variation","strand":1,"source":"dbSNP","start":140557529,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1303312888","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1426181964","clinical_significance":[],"end":140557531,"alleles":["ATA","-"],"strand":1,"feature_type":"variation","start":140557529,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["T","TGT","TT","TTT","TTTT","TTTTTTT"],"end":140557530,"feature_type":"variation","strand":1,"source":"dbSNP","start":140557530,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1563139283"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557530,"feature_type":"variation","strand":1,"alleles":["TATT","T"],"end":140557533,"clinical_significance":[],"seq_region_name":"7","id":"rs1797419155"},{"alleles":["TATTT","T"],"end":140557534,"strand":1,"feature_type":"variation","start":140557530,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1400824405","clinical_significance":[]},{"clinical_significance":[],"id":"rs1797419439","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557530,"feature_type":"variation","strand":1,"alleles":["TATTTTT","T"],"end":140557536},{"seq_region_name":"7","id":"rs1410044773","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557530,"source":"dbSNP","strand":1,"feature_type":"variation","end":140557538,"alleles":["TATTTTTTT","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557530,"feature_type":"variation","strand":1,"alleles":["TATTTTTTTT","T"],"end":140557539,"clinical_significance":[],"id":"rs1175467133","seq_region_name":"7"},{"start":140557530,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140557540,"alleles":["TATTTTTTTTT","T"],"strand":1,"feature_type":"variation","id":"rs1472138740","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557530,"feature_type":"variation","strand":1,"alleles":["TATTTTTTTTTT","T"],"end":140557541,"clinical_significance":[],"seq_region_name":"7","id":"rs1269337876"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1201788499","feature_type":"variation","strand":1,"alleles":["TATTTTTTTTTTT","T"],"end":140557542,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557530},{"alleles":["A","G","T"],"end":140557531,"feature_type":"variation","strand":1,"source":"dbSNP","start":140557531,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs867416988","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1223428438","seq_region_name":"7","source":"dbSNP","start":140557531,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","-"],"end":140557531,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1554467351","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","TATATATATATATATATATATATT","TATATATATATATATATATATATTT","TATATATATATATATATATATTTATTTT","TATATATATATATATATATGTT","TATATATATATATATATATGTTT","TATATATATATATATATATT","TATATATATATATATATATTT","TATATATATATATATATGTT","TATATATATATATATATT","TATATATATATATATATTT","TATATATATATATATATTTT","TATATATATATATATATTTTTTT","TATATATATATATATT","TATATATATATATATTT","TATATATATATATATTTT","TATATATATATATATTTTT","TATATATATATATATTTTTT","TATATATATATATTT","TATATATATATATTTT","TATATATATATATTTTT","TATATATATATATTTTTT","TATATATATATATTTTTTTT","TATATATATATGTATATTTT","TATATATATATGTATATTTTT","TATATATATATT","TATATATATATTTTTT","TATATATATATTTTTTT","TATATATATT","TATATATATTT","TATATATATTTT","TATATATATTTTTTTTT","TATATATT","TATATATTTATTTTTTTT","TATATATTTT","TATATATTTTT","TATATT","TATATTTT","TATATTTTT","TATATTTTTT","TATGTT","TATT","TATTT","TATTTT","TATTTTTT"],"end":140557532,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557532,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557532,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140557532,"id":"rs1563139307","seq_region_name":"7","clinical_significance":[]},{"alleles":["TTT","TTTATTTTTTTTTTTT"],"end":140557534,"strand":1,"feature_type":"variation","start":140557532,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797421521","clinical_significance":[]},{"seq_region_name":"7","id":"rs1156756617","clinical_significance":[],"alleles":["TTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT"],"end":140557557,"strand":1,"feature_type":"variation","start":140557532,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs71173208","end":140557532,"alleles":["-","A","ACA","ACATA","ATA","ATATA","ATATATA","ATATATAC","ATATATATA","ATATATATATA","ATATATATATATA","ATATATATATATATA","ATATATATATATATATA","ATATATATATATATATATA","ATATATATATATATATATATA","ATATATATATATATATATATATA","ATATATATATATATATATATG","ATATATATATATATATATG","ATATATATATATATATG","ATATATATATATATG","ATATATATATATG","ATATATATATGTATA","ATG","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140557533,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs7777506","source":"dbSNP","start":140557533,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A","G"],"end":140557533,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1554467353","source":"dbSNP","start":140557533,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140557533,"alleles":["T","TAAAATATATATATATATATATATAT"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140557533,"alleles":["-","A","ATA","ATATA","ATATATA","ATATATATA","ATATATATATA","ATATATATATATA","ATATATATATATATA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557534,"source":"dbSNP","seq_region_name":"7","id":"rs1563139334","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1263446238","alleles":["T","A"],"end":140557534,"feature_type":"variation","strand":1,"source":"dbSNP","start":140557534,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563139340","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557534,"feature_type":"variation","strand":1,"end":140557534,"alleles":["T","TAT","TATAT"]},{"strand":1,"feature_type":"variation","end":140557536,"alleles":["TTT","TTTATTT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557534,"source":"dbSNP","id":"rs1563139345","seq_region_name":"7","clinical_significance":[]},{"alleles":["-","A","ATA","ATATA","ATATATATA"],"end":140557534,"strand":1,"feature_type":"variation","start":140557535,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1563139348","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557535,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","G"],"end":140557535,"seq_region_name":"7","id":"rs369483351","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797424216","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["TTTTT","TTTTTCTTTTT"],"end":140557539,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557535,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557536,"feature_type":"variation","strand":1,"end":140557536,"alleles":["T","A"],"clinical_significance":[],"id":"rs1177683392","seq_region_name":"7"},{"id":"rs2130563864","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["TTTTT","TTTTTATTTTT"],"end":140557540,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557536,"source":"dbSNP"},{"source":"dbSNP","start":140557537,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140557537,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs373662616","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557538,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140557538,"seq_region_name":"7","id":"rs1471296609","clinical_significance":[]},{"seq_region_name":"7","id":"rs376356706","clinical_significance":[],"alleles":["T","A"],"end":140557539,"strand":1,"feature_type":"variation","start":140557539,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140557540,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557540,"source":"dbSNP","seq_region_name":"7","id":"rs1418042263","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130563905","end":140557541,"alleles":["TT","TTATT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140557540,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1425199819","feature_type":"variation","strand":1,"alleles":["T","A"],"end":140557541,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557541},{"id":"rs1162328296","seq_region_name":"7","clinical_significance":[],"alleles":["T","A"],"end":140557542,"strand":1,"feature_type":"variation","start":140557542,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140557543,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140557543,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1348493871"},{"feature_type":"variation","strand":1,"alleles":["-","A"],"end":140557543,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557544,"clinical_significance":[],"seq_region_name":"7","id":"rs1797425277"},{"source":"dbSNP","start":140557544,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140557544,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1457752106","seq_region_name":"7"},{"start":140557544,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140557544,"alleles":["T","TAT"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797425499","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140557545,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557545,"source":"dbSNP","id":"rs1299220115","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140557547,"alleles":["T","A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557547,"source":"dbSNP","seq_region_name":"7","id":"rs1585626103","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1294994553","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557548,"feature_type":"variation","strand":1,"alleles":["TTTTTTTTTTG","-"],"end":140557558},{"seq_region_name":"7","id":"rs1226993336","clinical_significance":[],"strand":1,"feature_type":"variation","end":140557558,"alleles":["TTTTTTTTTG","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557549,"source":"dbSNP"},{"source":"dbSNP","start":140557550,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140557558,"alleles":["TTTTTTTTG","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797426094"},{"seq_region_name":"7","id":"rs1797426211","clinical_significance":[],"start":140557551,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140557551,"alleles":["T","G"],"strand":1,"feature_type":"variation"},{"id":"rs1382955415","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140557552,"strand":1,"feature_type":"variation","start":140557552,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["-","C"],"end":140557552,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557553,"clinical_significance":[],"seq_region_name":"7","id":"rs1797426450"},{"alleles":["TTT","TTTTGTTT"],"end":140557557,"strand":1,"feature_type":"variation","start":140557555,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797426556","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797426668","clinical_significance":[],"start":140557555,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140557558,"alleles":["TTTG","-"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1797426786","seq_region_name":"7","source":"dbSNP","start":140557556,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140557556,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797426894","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557557,"feature_type":"variation","strand":1,"end":140557558,"alleles":["TG","-"]},{"feature_type":"variation","strand":1,"alleles":["-","TTTTA","TTTTTTTTTTG"],"end":140557557,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557558,"clinical_significance":[],"seq_region_name":"7","id":"rs1797426999"},{"feature_type":"variation","strand":1,"end":140557558,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557558,"clinical_significance":[],"id":"rs1317068844","seq_region_name":"7"},{"alleles":["G","-"],"end":140557558,"strand":1,"feature_type":"variation","start":140557558,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797427215","clinical_significance":[]},{"end":140557561,"alleles":["GAGA","GA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140557558,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797427308"},{"end":140557566,"alleles":["GAGACGGAG","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140557558,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1462631794"},{"seq_region_name":"7","id":"rs2130564087","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557558,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GAGACGGAG","G"],"end":140557566},{"start":140557559,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","-"],"end":140557559,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797427563","clinical_significance":[]},{"start":140557559,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140557559,"alleles":["A","T"],"strand":1,"feature_type":"variation","id":"rs2130564100","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140557560,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557560,"source":"dbSNP","id":"rs2130564119","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140557560,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","-"],"end":140557560,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130564129"},{"source":"dbSNP","start":140557562,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140557562,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1372965902"},{"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140557563,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557563,"source":"dbSNP","id":"rs1408029229","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557564,"feature_type":"variation","strand":1,"end":140557564,"alleles":["G","C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1797427955"},{"clinical_significance":[],"id":"rs2130564159","seq_region_name":"7","alleles":["A","T"],"end":140557565,"feature_type":"variation","strand":1,"source":"dbSNP","start":140557565,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1287827292","source":"dbSNP","start":140557566,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140557566,"alleles":["G","A","C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1463373070","clinical_significance":[],"end":140557568,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140557568,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs372294961","seq_region_name":"7","end":140557570,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140557570,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1356246470","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557571,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140557571},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797428609","end":140557577,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140557577,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","T"],"end":140557578,"strand":1,"feature_type":"variation","start":140557578,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1425376403","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140557579,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140557579,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1230237876","seq_region_name":"7"},{"start":140557583,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140557583,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1182219442","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797429053","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557586,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140557586},{"feature_type":"variation","strand":1,"end":140557587,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557587,"clinical_significance":[],"seq_region_name":"7","id":"rs1797429164"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557594,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140557594,"clinical_significance":[],"seq_region_name":"7","id":"rs368923113"},{"seq_region_name":"7","id":"rs1320867170","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557596,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140557596},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140557597,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557597,"clinical_significance":[],"seq_region_name":"7","id":"rs1585626250"},{"alleles":["C","T"],"end":140557600,"strand":1,"feature_type":"variation","start":140557600,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1204987851","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140557601,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140557601,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs866505567"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1276641159","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140557602,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557602},{"alleles":["G","T"],"end":140557603,"feature_type":"variation","strand":1,"source":"dbSNP","start":140557603,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797429975"},{"seq_region_name":"7","id":"rs1204081978","clinical_significance":[],"start":140557608,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140557608,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"alleles":["G","A"],"end":140557609,"strand":1,"feature_type":"variation","start":140557609,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1482035895","clinical_significance":[]},{"clinical_significance":[],"id":"rs1797430317","seq_region_name":"7","source":"dbSNP","start":140557610,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140557610,"alleles":["A","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1203739877","end":140557616,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140557616,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1797430527","clinical_significance":[],"start":140557621,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140557621,"strand":1,"feature_type":"variation"},{"start":140557624,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140557624,"strand":1,"feature_type":"variation","id":"rs1293350244","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140557625,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557625,"source":"dbSNP","id":"rs1242472034","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140557626,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140557626,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1339776986"},{"strand":1,"feature_type":"variation","end":140557628,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557628,"source":"dbSNP","seq_region_name":"7","id":"rs2130564360","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557632,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140557632,"seq_region_name":"7","id":"rs1022437331","clinical_significance":[]},{"source":"dbSNP","start":140557633,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140557633,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1392906855","seq_region_name":"7"},{"end":140557634,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140557634,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1348472924","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140557635,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557635,"source":"dbSNP","seq_region_name":"7","id":"rs1307582146","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585626380","alleles":["T","G"],"end":140557636,"feature_type":"variation","strand":1,"source":"dbSNP","start":140557636,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs967876443","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557639,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140557639},{"source":"dbSNP","start":140557640,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140557640,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1367473474"},{"start":140557641,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140557641,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1457505235","clinical_significance":[]},{"source":"dbSNP","start":140557642,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140557642,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1473531011","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1563139500","clinical_significance":[],"strand":1,"feature_type":"variation","end":140557648,"alleles":["TTCT","TTCTTCT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557645,"source":"dbSNP"},{"source":"dbSNP","start":140557647,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140557647,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797432100"},{"clinical_significance":[],"seq_region_name":"7","id":"rs977889387","source":"dbSNP","start":140557649,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140557649,"feature_type":"variation","strand":1},{"alleles":["T","C"],"end":140557651,"strand":1,"feature_type":"variation","start":140557651,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1030908751","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557656,"source":"dbSNP","strand":1,"feature_type":"variation","end":140557656,"alleles":["C","T"],"seq_region_name":"7","id":"rs1179717378","clinical_significance":[]},{"end":140557658,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140557658,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797432559","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557659,"source":"dbSNP","strand":1,"feature_type":"variation","end":140557659,"alleles":["C","A"],"seq_region_name":"7","id":"rs1797432693","clinical_significance":[]},{"alleles":["C","T"],"end":140557664,"strand":1,"feature_type":"variation","start":140557664,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797432808","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1412678620","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557665,"feature_type":"variation","strand":1,"end":140557665,"alleles":["G","A","C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1423549711","alleles":["T","A","G"],"end":140557666,"feature_type":"variation","strand":1,"source":"dbSNP","start":140557666,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1169653650","clinical_significance":[],"start":140557667,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140557667,"strand":1,"feature_type":"variation"},{"alleles":["GCTG","GCTGCTG"],"end":140557673,"feature_type":"variation","strand":1,"source":"dbSNP","start":140557670,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797433366"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557680,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140557680,"clinical_significance":[],"seq_region_name":"7","id":"rs1392512986"},{"source":"dbSNP","start":140557684,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140557684,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1270652090","seq_region_name":"7"},{"alleles":["G","A","C"],"end":140557685,"strand":1,"feature_type":"variation","start":140557685,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1428371834","clinical_significance":[]},{"end":140557686,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140557686,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1355109207","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1308035490","feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140557687,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557687},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140557688,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557688,"clinical_significance":[],"id":"rs1585626554","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797434282","feature_type":"variation","strand":1,"end":140557694,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557694},{"seq_region_name":"7","id":"rs12056060","clinical_significance":[],"start":140557695,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140557695,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140557696,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140557696,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1326747827"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557699,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140557699,"clinical_significance":[],"seq_region_name":"7","id":"rs1287511369"},{"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140557700,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557700,"source":"dbSNP","seq_region_name":"7","id":"rs1301268632","clinical_significance":[]},{"source":"dbSNP","start":140557701,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140557701,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs143725549"},{"clinical_significance":[],"id":"rs1797435145","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140557702,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557702},{"source":"dbSNP","start":140557704,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140557704,"alleles":["T","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797435258"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140557707,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557707,"source":"dbSNP","id":"rs1299559426","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557708,"feature_type":"variation","strand":1,"end":140557708,"alleles":["T","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585626664"},{"source":"dbSNP","start":140557713,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140557713,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1339871813"},{"alleles":["A","G"],"end":140557714,"strand":1,"feature_type":"variation","start":140557714,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1291074327","clinical_significance":[]},{"source":"dbSNP","start":140557719,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140557719,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1456135671"},{"clinical_significance":[],"id":"rs1227569881","seq_region_name":"7","source":"dbSNP","start":140557720,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140557720,"alleles":["A","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1281003024","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557726,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140557726},{"start":140557728,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A","C","G"],"end":140557728,"strand":1,"feature_type":"variation","id":"rs12056092","seq_region_name":"7","clinical_significance":[]},{"start":140557728,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140557728,"alleles":["T","-"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797436440","clinical_significance":[]},{"source":"dbSNP","start":140557729,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C","T"],"end":140557729,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs200067101"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557732,"source":"dbSNP","strand":1,"feature_type":"variation","end":140557732,"alleles":["G","A"],"seq_region_name":"7","id":"rs1797436751","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585626774","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557733,"feature_type":"variation","strand":1,"end":140557733,"alleles":["T","G"]},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140557738,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557738,"clinical_significance":[],"seq_region_name":"7","id":"rs1797436995"},{"seq_region_name":"7","id":"rs1797437138","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557743,"source":"dbSNP","strand":1,"feature_type":"variation","end":140557743,"alleles":["T","A"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557745,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140557745,"seq_region_name":"7","id":"rs1236493011","clinical_significance":[]},{"seq_region_name":"7","id":"rs1485991805","clinical_significance":[],"end":140557747,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140557747,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140557748,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140557748,"strand":1,"feature_type":"variation","id":"rs1797437468","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs992444760","end":140557755,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140557755,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140557757,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140557757,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1797437701","seq_region_name":"7"},{"start":140557759,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140557759,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","id":"rs1033944502","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140557760,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140557760,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1250287788"},{"alleles":["C","T"],"end":140557770,"feature_type":"variation","strand":1,"source":"dbSNP","start":140557770,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs2130564869","seq_region_name":"7"},{"alleles":["C","T"],"end":140557771,"strand":1,"feature_type":"variation","start":140557771,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs958453759","clinical_significance":[]},{"clinical_significance":[],"id":"rs1448092696","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557772,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140557772},{"seq_region_name":"7","id":"rs1267466707","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557773,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140557773},{"seq_region_name":"7","id":"rs973771743","clinical_significance":[],"end":140557774,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140557774,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140557776,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140557776,"alleles":["G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585626883","clinical_significance":[]},{"source":"dbSNP","start":140557777,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140557777,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs113043100","seq_region_name":"7"},{"start":140557778,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140557778,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs951277139","clinical_significance":[]},{"seq_region_name":"7","id":"rs550601255","clinical_significance":[],"start":140557780,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140557780,"strand":1,"feature_type":"variation"},{"end":140557781,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140557781,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1232811866","clinical_significance":[]},{"alleles":["C","T"],"end":140557782,"feature_type":"variation","strand":1,"source":"dbSNP","start":140557782,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1797438988","seq_region_name":"7"},{"end":140557784,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140557784,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs982743700","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1416205743","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557785,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140557785},{"seq_region_name":"7","id":"rs912467281","clinical_significance":[],"strand":1,"feature_type":"variation","end":140557786,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557786,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140557789,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557789,"source":"dbSNP","seq_region_name":"7","id":"rs562324607","clinical_significance":[]},{"seq_region_name":"7","id":"rs1436068067","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557790,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140557790},{"id":"rs1400527368","seq_region_name":"7","clinical_significance":[],"start":140557791,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140557791,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs948020647","seq_region_name":"7","alleles":["T","C"],"end":140557794,"feature_type":"variation","strand":1,"source":"dbSNP","start":140557794,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1797439898","clinical_significance":[],"start":140557797,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140557797,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140557799,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140557799,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs371634687"},{"clinical_significance":[],"seq_region_name":"7","id":"rs976087305","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140557803,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557803},{"end":140557806,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140557806,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs921888199"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140557817,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557817,"source":"dbSNP","seq_region_name":"7","id":"rs919991036","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1447183921","source":"dbSNP","start":140557818,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140557818,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797440574","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557820,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140557820},{"strand":1,"feature_type":"variation","end":140557821,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557821,"source":"dbSNP","id":"rs1797440686","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140557822,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557822,"clinical_significance":[],"seq_region_name":"7","id":"rs932072459"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557824,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140557824,"seq_region_name":"7","id":"rs1204300442","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557827,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140557827,"clinical_significance":[],"seq_region_name":"7","id":"rs1443860434"},{"end":140557828,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140557828,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1054515679","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs548471254","source":"dbSNP","start":140557829,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140557829,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs182479116","clinical_significance":[],"start":140557830,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C","T"],"end":140557830,"strand":1,"feature_type":"variation"},{"alleles":["C","T"],"end":140557831,"feature_type":"variation","strand":1,"source":"dbSNP","start":140557831,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1347072078"},{"seq_region_name":"7","id":"rs1797441606","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140557832,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557832,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557833,"feature_type":"variation","strand":1,"end":140557833,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1797441713"},{"start":140557834,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140557834,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs141929878","clinical_significance":[]},{"start":140557834,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140557835,"alleles":["GG","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797441977","clinical_significance":[]},{"end":140557837,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140557837,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1277284208","clinical_significance":[]},{"source":"dbSNP","start":140557838,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140557838,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1047254984"},{"seq_region_name":"7","id":"rs1304773450","clinical_significance":[],"start":140557840,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140557840,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140557842,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557842,"clinical_significance":[],"seq_region_name":"7","id":"rs1042009811"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797442602","feature_type":"variation","strand":1,"end":140557843,"alleles":["T","C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557843},{"strand":1,"feature_type":"variation","end":140557873,"alleles":["ATTTTTAAAATAGAGACAGGGCCTCATTTT","ATTTT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557844,"source":"dbSNP","seq_region_name":"7","id":"rs1797442724","clinical_significance":[]},{"start":140557845,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140557849,"alleles":["TTTTT","TTTT"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797442835","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797442925","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["ATA","A"],"end":140557855,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557853,"source":"dbSNP"},{"end":140557856,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140557856,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1339027569","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797443116","alleles":["A","G"],"end":140557857,"feature_type":"variation","strand":1,"source":"dbSNP","start":140557857,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557860,"source":"dbSNP","strand":1,"feature_type":"variation","end":140557860,"alleles":["C","A"],"seq_region_name":"7","id":"rs1210179300","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1410914869","source":"dbSNP","start":140557861,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AG","-"],"end":140557862,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140557863,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140557863,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1396738075"},{"seq_region_name":"7","id":"rs552711588","clinical_significance":[],"strand":1,"feature_type":"variation","end":140557864,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557864,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557866,"source":"dbSNP","strand":1,"feature_type":"variation","end":140557866,"alleles":["C","T"],"seq_region_name":"7","id":"rs1797444067","clinical_significance":[]},{"source":"dbSNP","start":140557868,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140557868,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs944307618","seq_region_name":"7"},{"end":140557874,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140557874,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797444392","clinical_significance":[]},{"start":140557880,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140557880,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs570964899","seq_region_name":"7","clinical_significance":[]},{"end":140557881,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140557881,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs537948754","clinical_significance":[]},{"start":140557882,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140557882,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797445052","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1188363856","feature_type":"variation","strand":1,"end":140557905,"alleles":["CTGGTCTCGAACTCCTGGTCTC","CTGGTCTCGAACTCCTGGTCTCGAACTCCTGGTCTC"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557884},{"clinical_significance":[],"id":"rs996234073","seq_region_name":"7","feature_type":"variation","strand":1,"end":140557891,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557891},{"strand":1,"feature_type":"variation","end":140557892,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557892,"source":"dbSNP","id":"rs1033996998","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs894119003","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140557906,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557906,"source":"dbSNP"},{"end":140557910,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140557910,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs995248654","clinical_significance":[]},{"seq_region_name":"7","id":"rs1226879227","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557913,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140557913},{"alleles":["T","A","C"],"end":140557914,"strand":1,"feature_type":"variation","start":140557914,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1277032532","clinical_significance":[]},{"start":140557915,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140557915,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797446437","clinical_significance":[]},{"clinical_significance":[],"id":"rs1746156047","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557918,"feature_type":"variation","strand":1,"end":140557918,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1203293658","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["CTTCT","CT"],"end":140557922,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557918,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797446824","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557921,"feature_type":"variation","strand":1,"end":140557921,"alleles":["C","T"]},{"id":"rs1797446969","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557924,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140557924},{"seq_region_name":"7","id":"rs758041625","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557927,"source":"dbSNP","strand":1,"feature_type":"variation","end":140557927,"alleles":["C","T"]},{"start":140557933,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140557933,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1341479981","clinical_significance":[]},{"source":"dbSNP","start":140557934,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140557934,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797447510"},{"clinical_significance":[],"seq_region_name":"7","id":"rs556546047","source":"dbSNP","start":140557935,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140557935,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1424543485","feature_type":"variation","strand":1,"alleles":["T","A"],"end":140557936,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557936},{"alleles":["G","A"],"end":140557937,"feature_type":"variation","strand":1,"source":"dbSNP","start":140557937,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1230490232"},{"clinical_significance":[],"id":"rs960797636","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557939,"feature_type":"variation","strand":1,"end":140557939,"alleles":["T","A"]},{"id":"rs992100908","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140557942,"strand":1,"feature_type":"variation","start":140557942,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140557943,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557943,"source":"dbSNP","seq_region_name":"7","id":"rs1797448091","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557954,"source":"dbSNP","strand":1,"feature_type":"variation","end":140557954,"alleles":["G","A"],"seq_region_name":"7","id":"rs1797448194","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557960,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140557960,"clinical_significance":[],"seq_region_name":"7","id":"rs2130565531"},{"alleles":["A","G"],"end":140557962,"strand":1,"feature_type":"variation","start":140557962,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797448319","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797448422","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140557963,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557963,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1023960109","clinical_significance":[],"alleles":["G","A"],"end":140557964,"strand":1,"feature_type":"variation","start":140557964,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs187132132","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140557965,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557965,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797448725","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557967,"feature_type":"variation","strand":1,"end":140557967,"alleles":["A","G"]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140557969,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557969,"clinical_significance":[],"seq_region_name":"7","id":"rs1407626157"},{"seq_region_name":"7","id":"rs1797448955","clinical_significance":[],"alleles":["T","C"],"end":140557970,"strand":1,"feature_type":"variation","start":140557970,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557970,"feature_type":"variation","strand":1,"alleles":["TTTTTT","TTTTTTT"],"end":140557975,"clinical_significance":[],"seq_region_name":"7","id":"rs1309397343"},{"clinical_significance":[],"id":"rs1797449191","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557971,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140557971},{"source":"dbSNP","start":140557978,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140557978,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130565600"},{"id":"rs191899204","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557981,"source":"dbSNP","strand":1,"feature_type":"variation","end":140557981,"alleles":["A","T"]},{"start":140557982,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140557982,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797449416","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140557992,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140557992,"clinical_significance":[],"seq_region_name":"7","id":"rs1456468232"},{"seq_region_name":"7","id":"rs1323971424","clinical_significance":[],"start":140557994,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140557994,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140557999,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140557999,"source":"dbSNP","seq_region_name":"7","id":"rs983014504","clinical_significance":[]},{"alleles":["A","C","T"],"end":140558000,"feature_type":"variation","strand":1,"source":"dbSNP","start":140558000,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs199771461"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797450052","end":140558007,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140558007,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797450165","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558010,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140558010},{"seq_region_name":"7","id":"rs1162659895","clinical_significance":[],"start":140558019,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140558019,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"id":"rs1470354179","seq_region_name":"7","clinical_significance":[],"start":140558023,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140558030,"alleles":["CTCCTCCT","CT","CTCCT"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140558030,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558030,"source":"dbSNP","seq_region_name":"7","id":"rs1434210952","clinical_significance":[]},{"seq_region_name":"7","id":"rs965290449","clinical_significance":[],"strand":1,"feature_type":"variation","end":140558033,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558033,"source":"dbSNP"},{"source":"dbSNP","start":140558035,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140558035,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797451136"},{"seq_region_name":"7","id":"rs1563139826","clinical_significance":[],"start":140558038,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140558038,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558040,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140558040,"seq_region_name":"7","id":"rs150667784","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs10252031","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558041,"feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140558041},{"end":140558042,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140558042,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs756386407","clinical_significance":[]},{"id":"rs1797452116","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558044,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140558044},{"source":"dbSNP","start":140558045,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140558045,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797452279"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558050,"source":"dbSNP","strand":1,"feature_type":"variation","end":140558050,"alleles":["C","T"],"seq_region_name":"7","id":"rs1797452451","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797452626","source":"dbSNP","start":140558052,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140558052,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797452806","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140558054,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558054},{"seq_region_name":"7","id":"rs1223831301","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558056,"source":"dbSNP","strand":1,"feature_type":"variation","end":140558056,"alleles":["C","T"]},{"source":"dbSNP","start":140558057,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","AA"],"end":140558057,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130565785"},{"seq_region_name":"7","id":"rs759384285","clinical_significance":[],"alleles":["C","T"],"end":140558058,"strand":1,"feature_type":"variation","start":140558058,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs866206797","source":"dbSNP","start":140558059,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140558059,"alleles":["G","A","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs900078242","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558061,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140558061},{"end":140558066,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140558066,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1797453860","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558068,"feature_type":"variation","strand":1,"end":140558068,"alleles":["A","C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs914637188"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130565827","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558070,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140558070},{"end":140558071,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140558071,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1226145207","clinical_significance":[]},{"id":"rs1349474505","seq_region_name":"7","clinical_significance":[],"start":140558076,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140558076,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs111518103","feature_type":"variation","strand":1,"alleles":["C","A","G","T"],"end":140558077,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558077},{"alleles":["T","G"],"end":140558078,"feature_type":"variation","strand":1,"source":"dbSNP","start":140558078,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797454577"},{"alleles":["G","A","C"],"end":140558080,"strand":1,"feature_type":"variation","start":140558080,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs77903254","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140558081,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558081,"clinical_significance":[],"seq_region_name":"7","id":"rs34228153"},{"seq_region_name":"7","id":"rs1797454940","clinical_significance":[],"end":140558085,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140558085,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140558087,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140558087,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1052104630","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558088,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140558088,"clinical_significance":[],"seq_region_name":"7","id":"rs1401244439"},{"start":140558090,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140558090,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130565902","clinical_significance":[]},{"clinical_significance":[],"id":"rs1313604558","seq_region_name":"7","source":"dbSNP","start":140558093,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140558093,"alleles":["G","A"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140558104,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558104,"source":"dbSNP","seq_region_name":"7","id":"rs1413856405","clinical_significance":[]},{"seq_region_name":"7","id":"rs12704002","clinical_significance":[],"start":140558107,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140558107,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1329782832","seq_region_name":"7","alleles":["G","A"],"end":140558108,"feature_type":"variation","strand":1,"source":"dbSNP","start":140558108,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558112,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140558112,"seq_region_name":"7","id":"rs1230228957","clinical_significance":[]},{"end":140558114,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140558114,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1266157193"},{"clinical_significance":[],"id":"rs1472168353","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558115,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140558115},{"seq_region_name":"7","id":"rs747766287","clinical_significance":[],"alleles":["C","G","T"],"end":140558118,"strand":1,"feature_type":"variation","start":140558118,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1222359468","clinical_significance":[],"strand":1,"feature_type":"variation","end":140558148,"alleles":["AGCAGAATGTACTCACCAGCAG","AGCAGAATGTACTCACCAGCAGAATGTACTCACCAGCAG"],"assembly_name":"GRCh38","consequence_type":"coding_sequence_variant","start":140558127,"source":"dbSNP"},{"start":140558128,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140558128,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1248708251","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558129,"source":"dbSNP","strand":1,"feature_type":"variation","end":140558129,"alleles":["C","A"],"seq_region_name":"7","id":"rs540725835","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140558133,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558133,"clinical_significance":[],"seq_region_name":"7","id":"rs1585627879"},{"seq_region_name":"7","id":"rs562519168","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140558134,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558134,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1487506229","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"splice_region_variant","start":140558135,"source":"dbSNP","strand":1,"feature_type":"variation","end":140558135,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1797457035","clinical_significance":[],"start":140558140,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_donor_region_variant","alleles":["C","T"],"end":140558140,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140558142,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"splice_donor_variant","start":140558142,"source":"dbSNP","seq_region_name":"7","id":"rs1190993703","clinical_significance":[]},{"id":"rs772723075","seq_region_name":"7","clinical_significance":[],"start":140558144,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140558144,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs760093160","clinical_significance":[],"alleles":["G","T"],"end":140558145,"strand":1,"feature_type":"variation","start":140558145,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"feature_type":"variation","strand":1,"end":140558146,"alleles":["C","G"],"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558146,"clinical_significance":[],"id":"rs1246213919","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs199683689","end":140558149,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140558149,"consequence_type":"synonymous_variant","assembly_name":"GRCh38"},{"id":"rs770542605","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140558153,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140558153},{"seq_region_name":"7","id":"rs1797457990","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140558156,"source":"dbSNP","strand":1,"feature_type":"variation","end":140558156,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1460238952","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140558159,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140558159,"source":"dbSNP"},{"seq_region_name":"7","id":"rs938952428","clinical_significance":["uncertain significance"],"start":140558163,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["C","T"],"end":140558163,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs776974525","seq_region_name":"7","consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558164,"feature_type":"variation","strand":1,"end":140558164,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs866062684","clinical_significance":[],"end":140558167,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140558167,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"id":"rs2130566187","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140558168,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140558168,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1433774431","source":"dbSNP","start":140558171,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140558171,"feature_type":"variation","strand":1},{"alleles":["G","T"],"end":140558173,"strand":1,"feature_type":"variation","start":140558173,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs1302145573","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs200609796","source":"dbSNP","start":140558176,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140558176,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1411404180","consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558179,"feature_type":"variation","strand":1,"end":140558179,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs765537033","clinical_significance":[],"strand":1,"feature_type":"variation","end":140558180,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140558180,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1349756021","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140558181,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140558181},{"seq_region_name":"7","id":"rs753091238","clinical_significance":[],"end":140558185,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140558185,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant"},{"strand":1,"feature_type":"variation","end":140558194,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140558194,"source":"dbSNP","seq_region_name":"7","id":"rs1292042943","clinical_significance":[]},{"id":"rs763094650","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140558199,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140558199,"source":"dbSNP"},{"seq_region_name":"7","id":"rs12704003","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140558200,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140558200},{"seq_region_name":"7","id":"rs751864937","clinical_significance":[],"start":140558201,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140558201,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs2486147056","clinical_significance":["uncertain significance"],"strand":1,"feature_type":"variation","end":140558202,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140558202,"source":"ClinVar"},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558205,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140558205,"clinical_significance":[],"seq_region_name":"7","id":"rs757276950"},{"feature_type":"variation","strand":1,"alleles":["AT","-"],"end":140558206,"consequence_type":"frameshift_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558205,"clinical_significance":[],"seq_region_name":"7","id":"rs866577469"},{"id":"rs2130566355","seq_region_name":"7","clinical_significance":[],"end":140558206,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140558206,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant"},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140558212,"source":"dbSNP","strand":1,"feature_type":"variation","end":140558212,"alleles":["A","C","G"],"seq_region_name":"7","id":"rs199820192","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1251764777","source":"dbSNP","start":140558213,"consequence_type":"splice_acceptor_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140558213,"feature_type":"variation","strand":1},{"alleles":["G","T"],"end":140558218,"feature_type":"variation","strand":1,"source":"dbSNP","start":140558218,"consequence_type":"splice_region_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs781371052"},{"seq_region_name":"7","id":"rs1318522309","clinical_significance":[],"start":140558219,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_region_variant","alleles":["T","C"],"end":140558219,"strand":1,"feature_type":"variation"},{"end":140558220,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140558220,"consequence_type":"splice_region_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585628213"},{"alleles":["ACACA","ACA"],"end":140558231,"feature_type":"variation","strand":1,"source":"dbSNP","start":140558227,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs750671378"},{"end":140558229,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140558229,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_polypyrimidine_tract_variant","id":"rs1797461439","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1048178353","source":"dbSNP","start":140558240,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140558240,"alleles":["A","T"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140558241,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558241,"clinical_significance":[],"seq_region_name":"7","id":"rs1467844175"},{"clinical_significance":[],"seq_region_name":"7","id":"rs753692786","feature_type":"variation","strand":1,"alleles":["A","T"],"end":140558244,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558244},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558245,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140558245,"seq_region_name":"7","id":"rs1403087569","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558247,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140558247,"seq_region_name":"7","id":"rs1797462061","clinical_significance":[]},{"alleles":["A","G"],"end":140558248,"feature_type":"variation","strand":1,"source":"dbSNP","start":140558248,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs754985483"},{"end":140558250,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140558250,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs969703091"},{"end":140558251,"alleles":["C","A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140558251,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1431432514","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1797462686","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558257,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140558257},{"source":"dbSNP","start":140558259,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140558259,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs778787178","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558260,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140558260,"seq_region_name":"7","id":"rs2130566512","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140558261,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558261,"clinical_significance":[],"seq_region_name":"7","id":"rs1797462894"},{"id":"rs1554467655","seq_region_name":"7","clinical_significance":[],"start":140558263,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140558263,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1585628339","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140558264,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558264},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797463175","end":140558265,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140558265,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs762722924","clinical_significance":[],"strand":1,"feature_type":"variation","end":140558266,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558266,"source":"dbSNP"},{"end":140558268,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140558268,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1214152600"},{"seq_region_name":"7","id":"rs1585628369","clinical_significance":[],"end":140558272,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140558272,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140558275,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140558275,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1187151035","clinical_significance":[]},{"clinical_significance":[],"id":"rs1797463757","seq_region_name":"7","source":"dbSNP","start":140558276,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140558276,"feature_type":"variation","strand":1},{"end":140558280,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140558280,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs768677795"},{"source":"dbSNP","start":140558282,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AA","AAA"],"end":140558283,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1403450634"},{"seq_region_name":"7","id":"rs2130566588","clinical_significance":[],"start":140558285,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140558285,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558288,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140558288,"clinical_significance":[],"seq_region_name":"7","id":"rs1797464097"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558289,"source":"dbSNP","strand":1,"feature_type":"variation","end":140558289,"alleles":["G","A"],"seq_region_name":"7","id":"rs548508254","clinical_significance":[]},{"id":"rs560447693","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558294,"source":"dbSNP","strand":1,"feature_type":"variation","end":140558294,"alleles":["T","C"]},{"alleles":["G","T"],"end":140558295,"feature_type":"variation","strand":1,"source":"dbSNP","start":140558295,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs182964986"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797464529","source":"dbSNP","start":140558299,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140558299,"feature_type":"variation","strand":1},{"start":140558301,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140558301,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1208655347","clinical_significance":[]},{"id":"rs1462001313","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140558302,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558302,"source":"dbSNP"},{"end":140558307,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140558307,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs995390237"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558308,"source":"dbSNP","strand":1,"feature_type":"variation","end":140558308,"alleles":["A","G"],"seq_region_name":"7","id":"rs1797464845","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797464958","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140558312,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558312},{"clinical_significance":[],"id":"rs114224605","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558318,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140558318},{"start":140558319,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140558319,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1371123240","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140558327,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558327,"source":"dbSNP","seq_region_name":"7","id":"rs1310046320","clinical_significance":[]},{"source":"dbSNP","start":140558328,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140558328,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs751297044"},{"end":140558340,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140558340,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1277541905","clinical_significance":[]},{"seq_region_name":"7","id":"rs1228473563","clinical_significance":[],"start":140558343,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140558343,"strand":1,"feature_type":"variation"},{"start":140558349,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140558349,"alleles":["A","AGGTA"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130566706","clinical_significance":[]},{"start":140558351,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140558351,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs759292654","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797465834","end":140558353,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140558353,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1797465939","clinical_significance":[],"end":140558355,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140558355,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs2130566730","seq_region_name":"7","source":"dbSNP","start":140558361,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140558362,"alleles":["CC","C"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558363,"source":"dbSNP","strand":1,"feature_type":"variation","end":140558363,"alleles":["A","G"],"seq_region_name":"7","id":"rs2130566742","clinical_significance":[]},{"start":140558364,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140558364,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797466053","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140558369,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558369,"clinical_significance":[],"seq_region_name":"7","id":"rs1797466160"},{"clinical_significance":[],"id":"rs1411058226","seq_region_name":"7","source":"dbSNP","start":140558374,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140558374,"alleles":["C","G"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558376,"feature_type":"variation","strand":1,"end":140558376,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs951338626"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130566771","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558377,"feature_type":"variation","strand":1,"end":140558377,"alleles":["G","A"]},{"end":140558378,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140558378,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1434295051"},{"seq_region_name":"7","id":"rs1349404576","clinical_significance":[],"end":140558381,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140558381,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558382,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140558382,"seq_region_name":"7","id":"rs982879157","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs996792487","source":"dbSNP","start":140558383,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140558383,"alleles":["C","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797467059","end":140558384,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140558384,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140558385,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558385,"clinical_significance":[],"seq_region_name":"7","id":"rs1797467169"},{"clinical_significance":[],"id":"rs965600659","seq_region_name":"7","feature_type":"variation","strand":1,"end":140558387,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558387},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140558389,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558389,"source":"dbSNP","seq_region_name":"7","id":"rs1797467395","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558393,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140558393,"clinical_significance":[],"seq_region_name":"7","id":"rs188557118"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558395,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140558395,"seq_region_name":"7","id":"rs1797467639","clinical_significance":[]},{"seq_region_name":"7","id":"rs538368550","clinical_significance":[],"start":140558397,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140558397,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1797467881","clinical_significance":[],"start":140558405,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140558405,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797468047","end":140558407,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140558407,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs947626989","source":"dbSNP","start":140558410,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140558410,"alleles":["A","T"],"feature_type":"variation","strand":1},{"end":140558411,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140558411,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs549970662"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140558412,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558412,"clinical_significance":[],"id":"rs1797468600","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558420,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140558420,"clinical_significance":[],"seq_region_name":"7","id":"rs568461894"},{"alleles":["C","A"],"end":140558421,"feature_type":"variation","strand":1,"source":"dbSNP","start":140558421,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130566935"},{"seq_region_name":"7","id":"rs1258928172","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558422,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140558422},{"seq_region_name":"7","id":"rs967886892","clinical_significance":[],"start":140558426,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140558426,"alleles":["T","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs924961457","clinical_significance":[],"end":140558430,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","start":140558430,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140558433,"alleles":["T","C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558433,"clinical_significance":[],"seq_region_name":"7","id":"rs1483159609"},{"seq_region_name":"7","id":"rs779046256","clinical_significance":[],"strand":1,"feature_type":"variation","end":140558434,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558434,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1236528608","source":"dbSNP","start":140558438,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140558438,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1205429654","clinical_significance":[],"start":140558439,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140558439,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558444,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140558444,"seq_region_name":"7","id":"rs977505913","clinical_significance":[]},{"alleles":["C","T"],"end":140558445,"feature_type":"variation","strand":1,"source":"dbSNP","start":140558445,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797470363"},{"clinical_significance":[],"id":"rs928836972","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558448,"feature_type":"variation","strand":1,"end":140558448,"alleles":["C","A","T"]},{"seq_region_name":"7","id":"rs1343600171","clinical_significance":[],"start":140558449,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140558449,"strand":1,"feature_type":"variation"},{"end":140558450,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140558450,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs938834574","seq_region_name":"7","clinical_significance":[]},{"end":140558451,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140558451,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1271886138","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558453,"feature_type":"variation","strand":1,"end":140558453,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1056014317"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558457,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140558457,"seq_region_name":"7","id":"rs1322218940","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558461,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140558461,"seq_region_name":"7","id":"rs2130567076","clinical_significance":[]},{"start":140558468,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140558468,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs376694002","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558469,"feature_type":"variation","strand":1,"end":140558469,"alleles":["G","A"],"clinical_significance":[],"id":"rs1797471792","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140558470,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558470,"clinical_significance":[],"seq_region_name":"7","id":"rs931532488"},{"seq_region_name":"7","id":"rs1394066845","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558472,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140558472},{"feature_type":"variation","strand":1,"end":140558473,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558473,"clinical_significance":[],"seq_region_name":"7","id":"rs1585628802"},{"seq_region_name":"7","id":"rs1482795078","clinical_significance":[],"alleles":["C","T"],"end":140558475,"strand":1,"feature_type":"variation","start":140558475,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1188483581","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558476,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140558476},{"start":140558478,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140558478,"alleles":["T","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1411925397","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797473143","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558480,"feature_type":"variation","strand":1,"end":140558480,"alleles":["G","A"]},{"id":"rs1368746936","seq_region_name":"7","clinical_significance":[],"start":140558487,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140558487,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797473479","feature_type":"variation","strand":1,"alleles":["GG","G"],"end":140558488,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558487},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130567183","source":"dbSNP","start":140558489,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140558489,"alleles":["A","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1254684933","end":140558491,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140558491,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558493,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140558493,"clinical_significance":[],"seq_region_name":"7","id":"rs1797473840"},{"feature_type":"variation","strand":1,"end":140558494,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558494,"clinical_significance":[],"id":"rs1048539750","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558497,"feature_type":"variation","strand":1,"end":140558497,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585628855"},{"end":140558498,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140558498,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1797474424","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797474543","source":"dbSNP","start":140558499,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140558499,"alleles":["C","G","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs192918468","seq_region_name":"7","source":"dbSNP","start":140558500,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140558500,"alleles":["C","T"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558501,"source":"dbSNP","strand":1,"feature_type":"variation","end":140558501,"alleles":["G","A"],"id":"rs1797474760","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140558503,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140558503,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1458521995"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558505,"source":"dbSNP","strand":1,"feature_type":"variation","end":140558505,"alleles":["G","A"],"seq_region_name":"7","id":"rs1004380644","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558506,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140558506,"seq_region_name":"7","id":"rs1471667245","clinical_significance":[]},{"alleles":["C","A"],"end":140558507,"feature_type":"variation","strand":1,"source":"dbSNP","start":140558507,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1162438833"},{"feature_type":"variation","strand":1,"end":140558509,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558509,"clinical_significance":[],"seq_region_name":"7","id":"rs1797475695"},{"start":140558511,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140558511,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1423532909","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140558512,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558512,"clinical_significance":[],"seq_region_name":"7","id":"rs1390651609"},{"seq_region_name":"7","id":"rs1431537640","clinical_significance":[],"end":140558513,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140558513,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140558515,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140558515,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs1797476408","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140558516,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558516,"source":"dbSNP","id":"rs1797476587","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1052159121","end":140558517,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140558517,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140558519,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558519,"clinical_significance":[],"seq_region_name":"7","id":"rs1797476959"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1182386493","alleles":["A","C"],"end":140558520,"feature_type":"variation","strand":1,"source":"dbSNP","start":140558520,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558521,"source":"dbSNP","strand":1,"feature_type":"variation","end":140558521,"alleles":["C","A"],"seq_region_name":"7","id":"rs1797477329","clinical_significance":[]},{"seq_region_name":"7","id":"rs1040784291","clinical_significance":[],"alleles":["G","C"],"end":140558525,"strand":1,"feature_type":"variation","start":140558525,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1797477694","clinical_significance":[],"end":140558530,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140558530,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558532,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140558532,"seq_region_name":"7","id":"rs1483849857","clinical_significance":[]},{"id":"rs1797478055","seq_region_name":"7","clinical_significance":[],"end":140558533,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140558533,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1797478276","seq_region_name":"7","clinical_significance":[],"start":140558541,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140558541,"strand":1,"feature_type":"variation"},{"end":140558546,"alleles":["AAAAA","AAAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140558542,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797478456"},{"clinical_significance":[],"id":"rs896221379","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140558543,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558543},{"feature_type":"variation","strand":1,"end":140558545,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558545,"clinical_significance":[],"seq_region_name":"7","id":"rs1797478794"},{"clinical_significance":[],"seq_region_name":"7","id":"rs12532573","feature_type":"variation","strand":1,"end":140558550,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558550},{"feature_type":"variation","strand":1,"end":140558551,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558551,"clinical_significance":[],"seq_region_name":"7","id":"rs1797479146"},{"start":140558554,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140558554,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1203781293","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs185489149","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558555,"feature_type":"variation","strand":1,"end":140558555,"alleles":["G","T"]},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140558556,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558556,"clinical_significance":[],"seq_region_name":"7","id":"rs1797479647"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558557,"source":"dbSNP","strand":1,"feature_type":"variation","end":140558557,"alleles":["A","T"],"seq_region_name":"7","id":"rs1013454442","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1045309204","source":"dbSNP","start":140558560,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140558560,"alleles":["G","A","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797480233","end":140558561,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140558561,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140558565,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140558565,"alleles":["A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797480402","clinical_significance":[]},{"seq_region_name":"7","id":"rs1320838890","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140558566,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558566,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797480580","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558571,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140558571},{"start":140558572,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140558572,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs752266100","clinical_significance":[]},{"clinical_significance":[],"id":"rs1288788286","seq_region_name":"7","feature_type":"variation","strand":1,"end":140558577,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558577},{"clinical_significance":[],"seq_region_name":"7","id":"rs1230051099","feature_type":"variation","strand":1,"end":140558579,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558579},{"strand":1,"feature_type":"variation","end":140558580,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558580,"source":"dbSNP","seq_region_name":"7","id":"rs772314832","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs901027517","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558589,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140558589},{"clinical_significance":[],"seq_region_name":"7","id":"rs1307724266","alleles":["G","T"],"end":140558591,"feature_type":"variation","strand":1,"source":"dbSNP","start":140558591,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797481637","feature_type":"variation","strand":1,"end":140558593,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558593},{"start":140558597,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140558597,"strand":1,"feature_type":"variation","id":"rs2130567620","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs904986661","clinical_significance":[],"start":140558599,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140558599,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558600,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140558600,"clinical_significance":[],"seq_region_name":"7","id":"rs996679568"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140558605,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558605,"source":"dbSNP","seq_region_name":"7","id":"rs1797483390","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140558606,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558606,"source":"dbSNP","seq_region_name":"7","id":"rs1026877049","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585629121","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558617,"source":"dbSNP","strand":1,"feature_type":"variation","end":140558617,"alleles":["A","C","G"]},{"source":"dbSNP","start":140558618,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140558618,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797483779"},{"seq_region_name":"7","id":"rs1457858888","clinical_significance":[],"start":140558619,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G","T"],"end":140558619,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558620,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140558620,"seq_region_name":"7","id":"rs1797484069","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140558621,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558621,"source":"dbSNP","seq_region_name":"7","id":"rs1028277343","clinical_significance":[]},{"source":"dbSNP","start":140558623,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140558623,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs951390645"},{"end":140558627,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140558627,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1161786606"},{"strand":1,"feature_type":"variation","end":140558628,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558628,"source":"dbSNP","id":"rs13247532","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","G"],"end":140558630,"feature_type":"variation","strand":1,"source":"dbSNP","start":140558630,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1797484804","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["-","TG"],"end":140558633,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558634,"clinical_significance":[],"seq_region_name":"7","id":"rs1338369376"},{"seq_region_name":"7","id":"rs558366788","clinical_significance":[],"strand":1,"feature_type":"variation","end":140558639,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558639,"source":"dbSNP"},{"id":"rs1022058431","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140558640,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558640,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558641,"feature_type":"variation","strand":1,"end":140558641,"alleles":["A","C"],"clinical_significance":[],"id":"rs1242978491","seq_region_name":"7"},{"start":140558645,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140558645,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1314807926","clinical_significance":[]},{"start":140558646,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140558646,"alleles":["A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1180653660","clinical_significance":[]},{"alleles":["A","T"],"end":140558648,"strand":1,"feature_type":"variation","start":140558648,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1433206554","clinical_significance":[]},{"id":"rs1797485881","seq_region_name":"7","clinical_significance":[],"start":140558649,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A","C"],"end":140558649,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1268869439","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558650,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140558650},{"end":140558652,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140558652,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1019726808"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558654,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140558654,"seq_region_name":"7","id":"rs1488101325","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558656,"source":"dbSNP","strand":1,"feature_type":"variation","end":140558656,"alleles":["A","C"],"id":"rs967392528","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558657,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140558657,"clinical_significance":[],"id":"rs1210349315","seq_region_name":"7"},{"source":"dbSNP","start":140558658,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140558658,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1343387200"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1231247817","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140558660,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558660},{"alleles":["C","A"],"end":140558662,"strand":1,"feature_type":"variation","start":140558662,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs977933394","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585629304","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558663,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140558663},{"id":"rs1035737277","seq_region_name":"7","clinical_significance":[],"start":140558664,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140558664,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558665,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140558665,"clinical_significance":[],"seq_region_name":"7","id":"rs960233469"},{"seq_region_name":"7","id":"rs1332854309","clinical_significance":[],"strand":1,"feature_type":"variation","end":140558666,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558666,"source":"dbSNP"},{"alleles":["G","A","C"],"end":140558667,"strand":1,"feature_type":"variation","start":140558667,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs965851216","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140558669,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140558669,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs112512507"},{"seq_region_name":"7","id":"rs1389987620","clinical_significance":[],"alleles":["T","C","G"],"end":140558670,"strand":1,"feature_type":"variation","start":140558670,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1455969957","seq_region_name":"7","source":"dbSNP","start":140558671,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["GGGGG","GGGG"],"end":140558675,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1585629378","clinical_significance":[],"end":140558677,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140558677,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130567994","feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140558678,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558678},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797488625","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558679,"feature_type":"variation","strand":1,"end":140558680,"alleles":["AA","A"]},{"id":"rs1388383400","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140558682,"strand":1,"feature_type":"variation","start":140558682,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558683,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140558683,"seq_region_name":"7","id":"rs190560434","clinical_significance":[]},{"source":"dbSNP","start":140558684,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140558684,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1258450338"},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140558685,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558685,"clinical_significance":[],"seq_region_name":"7","id":"rs2130568045"},{"id":"rs1585629423","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140558686,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558686,"source":"dbSNP"},{"alleles":["T","C"],"end":140558688,"strand":1,"feature_type":"variation","start":140558688,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797489376","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1379052631","end":140558690,"alleles":["T","TT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140558690,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1797489498","seq_region_name":"7","alleles":["T","C"],"end":140558690,"feature_type":"variation","strand":1,"source":"dbSNP","start":140558690,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140558691,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140558691,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1196107456","clinical_significance":[]},{"start":140558692,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A","C","G"],"end":140558692,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs562398404","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140558693,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558693,"source":"dbSNP","id":"rs2130568110","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797489959","feature_type":"variation","strand":1,"alleles":["T","A"],"end":140558694,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558694},{"alleles":["T","-"],"end":140558694,"feature_type":"variation","strand":1,"source":"dbSNP","start":140558694,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797490128"},{"start":140558695,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140558694,"alleles":["-","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797490318","clinical_significance":[]},{"alleles":["C","A"],"end":140558695,"strand":1,"feature_type":"variation","start":140558695,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1190434854","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1797490667","seq_region_name":"7","source":"dbSNP","start":140558695,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140558695,"alleles":["C","-"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1187178776","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140558696,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558696,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1232604188","alleles":["AAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAA","AAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAA"],"end":140558717,"feature_type":"variation","strand":1,"source":"dbSNP","start":140558696,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["-","G"],"end":140558696,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558697,"clinical_significance":[],"id":"rs1797491645","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1797491815","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558697,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140558697},{"end":140558702,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140558702,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1797491987","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140558704,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140558704,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1366106500"},{"source":"dbSNP","start":140558705,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140558705,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1248407343","seq_region_name":"7"},{"id":"rs1797492407","seq_region_name":"7","clinical_significance":[],"start":140558708,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140558708,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558711,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140558711,"seq_region_name":"7","id":"rs11973083","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1433556261","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558712,"feature_type":"variation","strand":1,"alleles":["-","C"],"end":140558711},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797492739","alleles":["A","C"],"end":140558713,"feature_type":"variation","strand":1,"source":"dbSNP","start":140558713,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1797492864","seq_region_name":"7","clinical_significance":[],"start":140558714,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140558713,"alleles":["-","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1797492959","clinical_significance":[],"start":140558715,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140558715,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140558720,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558720,"source":"dbSNP","id":"rs968827578","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1416569187","clinical_significance":[],"start":140558722,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140558722,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1389504961","feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140558723,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558723},{"strand":1,"feature_type":"variation","end":140558726,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558726,"source":"dbSNP","id":"rs1170520175","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558730,"source":"dbSNP","strand":1,"feature_type":"variation","end":140558730,"alleles":["G","C"],"id":"rs1797493576","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140558733,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558733,"clinical_significance":[],"id":"rs1585629573","seq_region_name":"7"},{"alleles":["A","G"],"end":140558737,"strand":1,"feature_type":"variation","start":140558737,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797493819","clinical_significance":[]},{"id":"rs979010458","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140558738,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558738,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1585629594","clinical_significance":[],"start":140558739,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140558739,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140558740,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140558740,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1173821332","seq_region_name":"7"},{"seq_region_name":"7","id":"rs551558466","clinical_significance":[],"strand":1,"feature_type":"variation","end":140558742,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558742,"source":"dbSNP"},{"end":140558744,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140558744,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs183741876"},{"seq_region_name":"7","id":"rs374417671","clinical_significance":[],"strand":1,"feature_type":"variation","end":140558745,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558745,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558746,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140558746,"id":"rs1320889414","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130568410","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558749,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140558749},{"clinical_significance":[],"seq_region_name":"7","id":"rs1187971231","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558751,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140558751},{"seq_region_name":"7","id":"rs2130568431","clinical_significance":[],"strand":1,"feature_type":"variation","end":140558755,"alleles":["GCCTG","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558751,"source":"dbSNP"},{"source":"dbSNP","start":140558753,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140558753,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1366354518"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558754,"feature_type":"variation","strand":1,"end":140558754,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130568465"},{"seq_region_name":"7","id":"rs1443982681","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558756,"source":"dbSNP","strand":1,"feature_type":"variation","end":140558756,"alleles":["A","-"]},{"strand":1,"feature_type":"variation","end":140558757,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558757,"source":"dbSNP","seq_region_name":"7","id":"rs2130568484","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140558759,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558759,"source":"dbSNP","seq_region_name":"7","id":"rs116566725","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130568514","alleles":["A","G"],"end":140558760,"feature_type":"variation","strand":1,"source":"dbSNP","start":140558760,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs2130568525","clinical_significance":[],"alleles":["TGT","-"],"end":140558766,"strand":1,"feature_type":"variation","start":140558764,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558765,"feature_type":"variation","strand":1,"end":140558765,"alleles":["G","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs867951291"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558766,"feature_type":"variation","strand":1,"end":140558766,"alleles":["T","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130568541"},{"id":"rs1210442025","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140558770,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558770,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558771,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140558771,"seq_region_name":"7","id":"rs1342900770","clinical_significance":[]},{"seq_region_name":"7","id":"rs567981329","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558772,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TTT","T"],"end":140558774},{"id":"rs2130568570","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140558773,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558773,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130568581","source":"dbSNP","start":140558775,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140558775,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140558776,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140558776,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797495649"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140558779,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558779,"clinical_significance":[],"seq_region_name":"7","id":"rs2130568597"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130568607","feature_type":"variation","strand":1,"end":140558781,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558781},{"end":140558783,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140558783,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs2130568617","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["CCTGGGC","C"],"end":140558789,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558783,"source":"dbSNP","seq_region_name":"7","id":"rs2130568621","clinical_significance":[]},{"start":140558784,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140558784,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs117335010","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558785,"source":"dbSNP","strand":1,"feature_type":"variation","end":140558785,"alleles":["T","G"],"seq_region_name":"7","id":"rs1233986330","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558786,"feature_type":"variation","strand":1,"end":140558786,"alleles":["G","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1797496005"},{"start":140558787,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140558787,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130568657","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140558789,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558789,"clinical_significance":[],"id":"rs1285365672","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558791,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140558791,"clinical_significance":[],"seq_region_name":"7","id":"rs2130568671"},{"seq_region_name":"7","id":"rs143354277","clinical_significance":[],"strand":1,"feature_type":"variation","end":140558792,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558792,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140558793,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558793,"clinical_significance":[],"seq_region_name":"7","id":"rs564318337"},{"clinical_significance":[],"id":"rs2130568707","seq_region_name":"7","feature_type":"variation","strand":1,"end":140558793,"alleles":["-","TTTTTT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558794},{"clinical_significance":[],"id":"rs2130568711","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558794,"feature_type":"variation","strand":1,"end":140558794,"alleles":["C","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558795,"feature_type":"variation","strand":1,"end":140558795,"alleles":["T","C"],"clinical_significance":[],"id":"rs1797496329","seq_region_name":"7"},{"start":140558798,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140558798,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797496443","clinical_significance":[]},{"source":"dbSNP","start":140558799,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140558799,"alleles":["A","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1585629782","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1797496682","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140558801,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558801,"source":"dbSNP"},{"seq_region_name":"7","id":"rs139979721","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558806,"source":"dbSNP","strand":1,"feature_type":"variation","end":140558806,"alleles":["C","T"]},{"feature_type":"variation","strand":1,"end":140558806,"alleles":["-","CT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558807,"clinical_significance":[],"seq_region_name":"7","id":"rs1797496902"},{"clinical_significance":[],"seq_region_name":"7","id":"rs34152911","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558807,"feature_type":"variation","strand":1,"alleles":["TTTTTTTTTTTTT","TTTTTTTTTTTT","TTTTTTTTTTTTTT","TTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTT"],"end":140558819},{"alleles":["-","C"],"end":140558807,"feature_type":"variation","strand":1,"source":"dbSNP","start":140558808,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1203239314"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1163836159","end":140558808,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140558808,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558812,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["-","C"],"end":140558811,"seq_region_name":"7","id":"rs1797497566","clinical_significance":[]},{"id":"rs905040012","seq_region_name":"7","clinical_significance":[],"start":140558813,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140558812,"alleles":["-","G"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140558813,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558813,"clinical_significance":[],"seq_region_name":"7","id":"rs2130568823"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558820,"feature_type":"variation","strand":1,"end":140558820,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1290625712"},{"end":140558820,"alleles":["C","CC"],"strand":1,"feature_type":"variation","start":140558820,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797497890","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797498026","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558822,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140558822},{"clinical_significance":[],"seq_region_name":"7","id":"rs1366522572","source":"dbSNP","start":140558825,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140558825,"alleles":["T","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1797498238","seq_region_name":"7","source":"dbSNP","start":140558826,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140558827,"alleles":["GG","G"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140558828,"alleles":["A","C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558828,"clinical_significance":[],"seq_region_name":"7","id":"rs1187444271"},{"alleles":["C","A"],"end":140558831,"strand":1,"feature_type":"variation","start":140558831,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1483488395","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1254307081","clinical_significance":[],"end":140558833,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140558833,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140558836,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140558836,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797498726","clinical_significance":[]},{"clinical_significance":[],"id":"rs1466048904","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558837,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140558837},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558838,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140558838,"clinical_significance":[],"seq_region_name":"7","id":"rs531375148"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797499115","source":"dbSNP","start":140558841,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140558841,"alleles":["T","G"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140558842,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558842,"clinical_significance":[],"seq_region_name":"7","id":"rs1797499225"},{"seq_region_name":"7","id":"rs1291140299","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140558843,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558843,"source":"dbSNP"},{"start":140558844,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140558844,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797499433","clinical_significance":[]},{"seq_region_name":"7","id":"rs1230545912","clinical_significance":[],"start":140558848,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140558848,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs931122575","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C","T"],"end":140558852,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558852,"source":"dbSNP"},{"end":140558855,"alleles":["T","C","G"],"strand":1,"feature_type":"variation","start":140558855,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs550250140","clinical_significance":[]},{"end":140558858,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140558858,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1433709765"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1350700467","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140558860,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558860},{"seq_region_name":"7","id":"rs568503853","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558863,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140558863},{"clinical_significance":[],"seq_region_name":"7","id":"rs1309531720","end":140558864,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140558864,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1407447915","alleles":["C","T"],"end":140558869,"feature_type":"variation","strand":1,"source":"dbSNP","start":140558869,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1797500468","clinical_significance":[],"alleles":["T","G"],"end":140558870,"strand":1,"feature_type":"variation","start":140558870,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140558871,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140558871,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1200981582","clinical_significance":[]},{"seq_region_name":"7","id":"rs1407045782","clinical_significance":[],"start":140558872,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140558872,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140558873,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558873,"clinical_significance":[],"id":"rs868386097","seq_region_name":"7"},{"alleles":["C","T"],"end":140558876,"feature_type":"variation","strand":1,"source":"dbSNP","start":140558876,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs916041773"},{"start":140558877,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140558877,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs931574357","clinical_significance":[]},{"end":140558880,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140558880,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs984359414","clinical_significance":[]},{"seq_region_name":"7","id":"rs1472830817","clinical_significance":[],"strand":1,"feature_type":"variation","end":140558881,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558881,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558884,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140558884,"clinical_significance":[],"seq_region_name":"7","id":"rs529345520"},{"seq_region_name":"7","id":"rs1797501294","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140558885,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558885,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558891,"feature_type":"variation","strand":1,"end":140558891,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1172758736"},{"end":140558892,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140558892,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs10275505"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558894,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140558894,"id":"rs1797501668","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs939682360","clinical_significance":[],"start":140558895,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140558895,"alleles":["C","A","G","T"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558896,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140558896,"clinical_significance":[],"seq_region_name":"7","id":"rs1040855283"},{"feature_type":"variation","strand":1,"end":140558897,"alleles":["G","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558897,"clinical_significance":[],"seq_region_name":"7","id":"rs1797501948"},{"seq_region_name":"7","id":"rs1585630125","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558899,"source":"dbSNP","strand":1,"feature_type":"variation","end":140558899,"alleles":["T","G"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558903,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140558903,"seq_region_name":"7","id":"rs2130569196","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558905,"source":"dbSNP","strand":1,"feature_type":"variation","end":140558905,"alleles":["C","A","T"],"seq_region_name":"7","id":"rs900914971","clinical_significance":[]},{"alleles":["G","C"],"end":140558906,"feature_type":"variation","strand":1,"source":"dbSNP","start":140558906,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs901148829"},{"feature_type":"variation","strand":1,"end":140558907,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558907,"clinical_significance":[],"seq_region_name":"7","id":"rs1797502455"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585630148","source":"dbSNP","start":140558908,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140558908,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140558910,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558910,"source":"dbSNP","id":"rs1273159551","seq_region_name":"7","clinical_significance":[]},{"id":"rs1797502814","seq_region_name":"7","clinical_significance":[],"start":140558912,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140558912,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140558913,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558913,"clinical_significance":[],"seq_region_name":"7","id":"rs1797502957"},{"clinical_significance":[],"seq_region_name":"7","id":"rs997351879","feature_type":"variation","strand":1,"end":140558915,"alleles":["G","A","C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558915},{"source":"dbSNP","start":140558917,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140558917,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1390426846"},{"clinical_significance":[],"id":"rs1459096237","seq_region_name":"7","alleles":["C","T"],"end":140558919,"feature_type":"variation","strand":1,"source":"dbSNP","start":140558919,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs867169287","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558922,"feature_type":"variation","strand":1,"end":140558922,"alleles":["C","G","T"]},{"seq_region_name":"7","id":"rs1797503647","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558922,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","-"],"end":140558922},{"seq_region_name":"7","id":"rs932355527","clinical_significance":[],"start":140558923,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140558923,"alleles":["G","A","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1049590296","feature_type":"variation","strand":1,"end":140558929,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558929},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558937,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140558937,"seq_region_name":"7","id":"rs1797504000","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["AA","AAA"],"end":140558947,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558946,"clinical_significance":[],"seq_region_name":"7","id":"rs1797504112"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558948,"feature_type":"variation","strand":1,"end":140558948,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1797504243"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585630251","source":"dbSNP","start":140558950,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140558950,"alleles":["G","A"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140558955,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140558955,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1329263281"},{"clinical_significance":[],"id":"rs1797504547","seq_region_name":"7","source":"dbSNP","start":140558956,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["CCATC","CCATCCATC"],"end":140558960,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1361771754","clinical_significance":[],"alleles":["T","C"],"end":140558963,"strand":1,"feature_type":"variation","start":140558963,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140558964,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140558964,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1387856651"},{"end":140558966,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140558966,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797504966","clinical_significance":[]},{"seq_region_name":"7","id":"rs893615753","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558970,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140558970},{"seq_region_name":"7","id":"rs1457516699","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558973,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140558973},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558976,"source":"dbSNP","strand":1,"feature_type":"variation","end":140558976,"alleles":["C","A","T"],"seq_region_name":"7","id":"rs1028393999","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797505434","clinical_significance":[],"alleles":["C","A","G"],"end":140558979,"strand":1,"feature_type":"variation","start":140558979,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1797505559","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140558984,"source":"dbSNP","strand":1,"feature_type":"variation","end":140558984,"alleles":["T","C"]},{"clinical_significance":[],"id":"rs2130569446","seq_region_name":"7","feature_type":"variation","strand":1,"end":140558987,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558987},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797505660","feature_type":"variation","strand":1,"end":140558998,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140558998},{"seq_region_name":"7","id":"rs1797505778","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559010,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140559010},{"source":"dbSNP","start":140559011,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140559011,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1011270406","seq_region_name":"7"},{"seq_region_name":"7","id":"rs968881320","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559014,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140559014},{"seq_region_name":"7","id":"rs778207406","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140559015,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559015,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1329393335","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140559023,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559023},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797506356","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559025,"feature_type":"variation","strand":1,"end":140559025,"alleles":["G","C"]},{"start":140559026,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140559026,"strand":1,"feature_type":"variation","id":"rs1797506463","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559027,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140559027,"seq_region_name":"7","id":"rs1797506571","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559032,"source":"dbSNP","strand":1,"feature_type":"variation","end":140559032,"alleles":["G","A"],"seq_region_name":"7","id":"rs1797506679","clinical_significance":[]},{"seq_region_name":"7","id":"rs188456420","clinical_significance":[],"alleles":["G","A","T"],"end":140559034,"strand":1,"feature_type":"variation","start":140559034,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs565723636","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559035,"source":"dbSNP","strand":1,"feature_type":"variation","end":140559035,"alleles":["C","G"]},{"clinical_significance":[],"id":"rs1223006782","seq_region_name":"7","source":"dbSNP","start":140559036,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140559036,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs956298968","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559041,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140559041},{"source":"dbSNP","start":140559048,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140559048,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1331489604","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1563140669","seq_region_name":"7","source":"dbSNP","start":140559049,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140559049,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140559051,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559051,"clinical_significance":[],"id":"rs1797507395","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140559054,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559054,"source":"dbSNP","id":"rs1585630415","seq_region_name":"7","clinical_significance":[]},{"alleles":["GAACTGAG","G"],"end":140559062,"strand":1,"feature_type":"variation","start":140559055,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1215573584","clinical_significance":[]},{"end":140559058,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140559058,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1315941379","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559059,"feature_type":"variation","strand":1,"end":140559059,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs377408236"},{"seq_region_name":"7","id":"rs1220450801","clinical_significance":[],"start":140559060,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140559060,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140559061,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140559061,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797508030"},{"seq_region_name":"7","id":"rs747403515","clinical_significance":[],"start":140559064,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140559064,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559065,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140559065,"clinical_significance":[],"seq_region_name":"7","id":"rs1206523151"},{"start":140559073,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140559073,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1302519458","clinical_significance":[]},{"end":140559074,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140559074,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797508468","clinical_significance":[]},{"clinical_significance":[],"id":"rs1797508566","seq_region_name":"7","source":"dbSNP","start":140559077,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140559077,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797508661","end":140559078,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140559078,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140559091,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140559091,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797508780"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559093,"feature_type":"variation","strand":1,"end":140559096,"alleles":["TAGG","-"],"clinical_significance":[],"seq_region_name":"7","id":"rs1797508966"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797509159","source":"dbSNP","start":140559093,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TAGGGATGTGACT","-"],"end":140559105,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559096,"feature_type":"variation","strand":1,"end":140559096,"alleles":["G","A"],"clinical_significance":[],"id":"rs1435758002","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1461140086","source":"dbSNP","start":140559098,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140559098,"alleles":["A","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1367037534","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559099,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140559099},{"seq_region_name":"7","id":"rs1797509860","clinical_significance":[],"start":140559104,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["CTC","C"],"end":140559106,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140559105,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140559105,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1035623245"},{"seq_region_name":"7","id":"rs949053453","clinical_significance":[],"alleles":["C","T"],"end":140559106,"strand":1,"feature_type":"variation","start":140559106,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs960118643","end":140559107,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140559107,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1178588024","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559110,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140559110},{"seq_region_name":"7","id":"rs1797510463","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["GAGGGAG","G"],"end":140559116,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559110,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140559112,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559112,"source":"dbSNP","seq_region_name":"7","id":"rs1797510588","clinical_significance":[]},{"source":"dbSNP","start":140559114,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["-","CA"],"end":140559113,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs747682206"},{"feature_type":"variation","strand":1,"end":140559117,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559117,"clinical_significance":[],"seq_region_name":"7","id":"rs113632044"},{"seq_region_name":"7","id":"rs867408526","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559119,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140559119},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559120,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140559120,"clinical_significance":[],"seq_region_name":"7","id":"rs1451847679"},{"start":140559121,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140559121,"strand":1,"feature_type":"variation","id":"rs1265212946","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797511261","clinical_significance":[],"start":140559131,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140559131,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140559132,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140559132,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1797511359","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1797511454","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559133,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140559133},{"seq_region_name":"7","id":"rs140324245","clinical_significance":[],"start":140559135,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140559135,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1797511693","clinical_significance":[],"start":140559137,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140559137,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"start":140559142,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140559142,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797511805","clinical_significance":[]},{"seq_region_name":"7","id":"rs1326947378","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559144,"source":"dbSNP","strand":1,"feature_type":"variation","end":140559144,"alleles":["C","G"]},{"clinical_significance":[],"id":"rs1797511992","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559147,"feature_type":"variation","strand":1,"end":140559147,"alleles":["T","-"]},{"strand":1,"feature_type":"variation","end":140559148,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559148,"source":"dbSNP","id":"rs1585630586","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559154,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140559154,"id":"rs1797512209","seq_region_name":"7","clinical_significance":[]},{"start":140559155,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140559155,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs984801189","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797512424","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559159,"source":"dbSNP","strand":1,"feature_type":"variation","end":140559159,"alleles":["C","G"]},{"end":140559161,"alleles":["T","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140559161,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1237628184"},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140559163,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559163,"clinical_significance":[],"seq_region_name":"7","id":"rs570235967"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140559165,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559165,"clinical_significance":[],"seq_region_name":"7","id":"rs2130569987"},{"feature_type":"variation","strand":1,"end":140559166,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559166,"clinical_significance":[],"id":"rs2130570000","seq_region_name":"7"},{"id":"rs1797512635","seq_region_name":"7","clinical_significance":[],"start":140559170,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140559170,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140559171,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559171,"source":"dbSNP","seq_region_name":"7","id":"rs1797512736","clinical_significance":[]},{"start":140559176,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140559176,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs754213024","clinical_significance":[]},{"id":"rs1048263580","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140559183,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559183,"source":"dbSNP"},{"id":"rs1797513089","seq_region_name":"7","clinical_significance":[],"start":140559184,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["GTCTGTA","-"],"end":140559190,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140559185,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559185,"source":"dbSNP","seq_region_name":"7","id":"rs939715693","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs976422874","source":"dbSNP","start":140559196,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140559196,"alleles":["C","A"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140559200,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559200,"source":"dbSNP","seq_region_name":"7","id":"rs1228546571","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140559202,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559202,"clinical_significance":[],"id":"rs1413646137","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559203,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140559203,"seq_region_name":"7","id":"rs537209176","clinical_significance":[]},{"source":"dbSNP","start":140559206,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140559206,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1344193889"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559207,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CTTGGACGGTCCTT","CTT"],"end":140559220,"seq_region_name":"7","id":"rs772561375","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140559208,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559208,"clinical_significance":[],"seq_region_name":"7","id":"rs1293416508"},{"clinical_significance":[],"seq_region_name":"7","id":"rs932407823","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140559213,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559213},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559214,"feature_type":"variation","strand":1,"end":140559214,"alleles":["G","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs555917438"},{"seq_region_name":"7","id":"rs2130570130","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140559224,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559224,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1797514295","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559226,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140559226},{"source":"dbSNP","start":140559228,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140559228,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130570140"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559230,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140559230,"clinical_significance":[],"seq_region_name":"7","id":"rs1797514386"},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140559236,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559236,"source":"dbSNP","id":"rs1585630715","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797514581","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559239,"feature_type":"variation","strand":1,"end":140559239,"alleles":["C","T"]},{"start":140559241,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140559241,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797514706","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140559245,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559245,"clinical_significance":[],"seq_region_name":"7","id":"rs1344946397"},{"clinical_significance":[],"seq_region_name":"7","id":"rs893654123","source":"dbSNP","start":140559248,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","G","T"],"end":140559248,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585630745","end":140559249,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140559249,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1295750276","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559250,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140559250},{"seq_region_name":"7","id":"rs574630406","clinical_significance":[],"end":140559251,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140559251,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["G","A"],"end":140559252,"feature_type":"variation","strand":1,"source":"dbSNP","start":140559252,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1404338763"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559255,"source":"dbSNP","strand":1,"feature_type":"variation","end":140559255,"alleles":["C","T"],"seq_region_name":"7","id":"rs1797515563","clinical_significance":[]},{"clinical_significance":[],"id":"rs1797515658","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559259,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140559259},{"source":"dbSNP","start":140559261,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140559261,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1042734478"},{"alleles":["A","G"],"end":140559265,"feature_type":"variation","strand":1,"source":"dbSNP","start":140559265,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1797515871","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797515961","feature_type":"variation","strand":1,"end":140559266,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559266},{"seq_region_name":"7","id":"rs1797516069","clinical_significance":[],"strand":1,"feature_type":"variation","end":140559272,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559272,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797516182","source":"dbSNP","start":140559273,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140559273,"alleles":["C","T"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140559274,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559274,"source":"dbSNP","seq_region_name":"7","id":"rs902438032","clinical_significance":[]},{"id":"rs771216137","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559276,"source":"dbSNP","strand":1,"feature_type":"variation","end":140559276,"alleles":["A","-"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559276,"source":"dbSNP","strand":1,"feature_type":"variation","end":140559276,"alleles":["A","AA"],"seq_region_name":"7","id":"rs1431768982","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797516403","clinical_significance":[],"alleles":["A","G"],"end":140559276,"strand":1,"feature_type":"variation","start":140559276,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797516894","alleles":["A","C"],"end":140559281,"feature_type":"variation","strand":1,"source":"dbSNP","start":140559281,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","T"],"end":140559282,"strand":1,"feature_type":"variation","start":140559282,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1563140773","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1003377408","source":"dbSNP","start":140559283,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140559283,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140559287,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140559287,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs541923806"},{"alleles":["C","A","T"],"end":140559292,"feature_type":"variation","strand":1,"source":"dbSNP","start":140559292,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs904608618"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797517483","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140559295,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559295},{"start":140559297,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140559297,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1416445314","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585630911","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559298,"feature_type":"variation","strand":1,"end":140559298,"alleles":["G","A"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559299,"source":"dbSNP","strand":1,"feature_type":"variation","end":140559299,"alleles":["C","A","T"],"seq_region_name":"7","id":"rs181090568","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140559300,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559300,"clinical_significance":[],"seq_region_name":"7","id":"rs757615863"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559301,"source":"dbSNP","strand":1,"feature_type":"variation","end":140559301,"alleles":["G","C"],"id":"rs1797518067","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130570399","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140559302,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559302},{"alleles":["T","A"],"end":140559307,"strand":1,"feature_type":"variation","start":140559307,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797518178","clinical_significance":[]},{"seq_region_name":"7","id":"rs566672450","clinical_significance":[],"end":140559309,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140559309,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1205234031","clinical_significance":[],"alleles":["G","C"],"end":140559310,"strand":1,"feature_type":"variation","start":140559310,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1031804237","clinical_significance":[],"start":140559312,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140559312,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140559322,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559322,"clinical_significance":[],"seq_region_name":"7","id":"rs2130570460"},{"clinical_significance":[],"seq_region_name":"7","id":"rs956184578","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559324,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140559324},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797518724","end":140559328,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140559328,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559331,"source":"dbSNP","strand":1,"feature_type":"variation","end":140559331,"alleles":["T","C"],"seq_region_name":"7","id":"rs1797518842","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559334,"source":"dbSNP","strand":1,"feature_type":"variation","end":140559334,"alleles":["T","C"],"seq_region_name":"7","id":"rs2130570494","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140559336,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559336,"source":"dbSNP","seq_region_name":"7","id":"rs1203749670","clinical_significance":[]},{"start":140559338,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140559338,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","id":"rs1322048145","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140559339,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559339,"source":"dbSNP","seq_region_name":"7","id":"rs1314647894","clinical_significance":[]},{"id":"rs58620263","seq_region_name":"7","clinical_significance":[],"start":140559340,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140559340,"strand":1,"feature_type":"variation"},{"id":"rs1797519402","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140559348,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559348,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797519478","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559349,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140559349},{"clinical_significance":[],"seq_region_name":"7","id":"rs1024548446","source":"dbSNP","start":140559352,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140559352,"alleles":["A","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs970825707","feature_type":"variation","strand":1,"end":140559356,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559356},{"seq_region_name":"7","id":"rs1411667729","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140559358,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559358,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559360,"source":"dbSNP","strand":1,"feature_type":"variation","end":140559360,"alleles":["A","G"],"seq_region_name":"7","id":"rs1797519928","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140559361,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559361,"source":"dbSNP","seq_region_name":"7","id":"rs1012982051","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559362,"feature_type":"variation","strand":1,"end":140559362,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs746054199"},{"source":"dbSNP","start":140559368,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140559368,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797520274"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1263539206","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559373,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140559373},{"feature_type":"variation","strand":1,"end":140559374,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559374,"clinical_significance":[],"id":"rs1797520519","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1490171051","end":140559376,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140559376,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140559380,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140559380,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797520736"},{"seq_region_name":"7","id":"rs1298060767","clinical_significance":[],"start":140559381,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140559381,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140559382,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559382,"clinical_significance":[],"seq_region_name":"7","id":"rs1356607751"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1022984463","source":"dbSNP","start":140559389,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140559389,"feature_type":"variation","strand":1},{"start":140559391,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140559391,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs527536245","clinical_significance":[]},{"end":140559394,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140559394,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1005711005"},{"feature_type":"variation","strand":1,"end":140559404,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559404,"clinical_significance":[],"seq_region_name":"7","id":"rs1016142574"},{"source":"dbSNP","start":140559405,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140559405,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797521403"},{"id":"rs980462920","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559406,"source":"dbSNP","strand":1,"feature_type":"variation","end":140559406,"alleles":["T","C"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559420,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140559420,"clinical_significance":[],"seq_region_name":"7","id":"rs184840762"},{"source":"dbSNP","start":140559421,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140559421,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs931050557"},{"alleles":["G","A"],"end":140559422,"feature_type":"variation","strand":1,"source":"dbSNP","start":140559422,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1797521879","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140559424,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559424,"clinical_significance":[],"seq_region_name":"7","id":"rs1416707174"},{"id":"rs34950336","seq_region_name":"7","clinical_significance":[],"start":140559425,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140559426,"alleles":["AA","AAA"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559436,"source":"dbSNP","strand":1,"feature_type":"variation","end":140559436,"alleles":["T","G"],"id":"rs1182454404","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs961652108","clinical_significance":[],"end":140559437,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140559437,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140559443,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140559443,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1473252845"},{"seq_region_name":"7","id":"rs976977918","clinical_significance":[],"start":140559448,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140559448,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs34678721","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559449,"feature_type":"variation","strand":1,"alleles":["CCC","CCCC"],"end":140559451},{"clinical_significance":[],"seq_region_name":"7","id":"rs1195114435","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559451,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140559451},{"seq_region_name":"7","id":"rs1267210667","clinical_significance":[],"alleles":["G","A"],"end":140559454,"strand":1,"feature_type":"variation","start":140559454,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140559456,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140559456,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1211585789","seq_region_name":"7"},{"start":140559458,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140559458,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1333895181","clinical_significance":[]},{"id":"rs1797523314","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140559463,"strand":1,"feature_type":"variation","start":140559463,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1797523479","clinical_significance":[],"start":140559464,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140559464,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140559465,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559465,"source":"dbSNP","seq_region_name":"7","id":"rs531541459","clinical_significance":[]},{"id":"rs1230490689","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559466,"source":"dbSNP","strand":1,"feature_type":"variation","end":140559466,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs149688051","clinical_significance":[],"alleles":["C","T"],"end":140559470,"strand":1,"feature_type":"variation","start":140559470,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs953675351","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559471,"feature_type":"variation","strand":1,"end":140559471,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797524380","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559475,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140559475},{"start":140559478,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140559478,"alleles":["T","G"],"strand":1,"feature_type":"variation","id":"rs1176247115","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140559480,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140559480,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs985247760"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559481,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140559481,"clinical_significance":[],"id":"rs1797524897","seq_region_name":"7"},{"seq_region_name":"7","id":"rs190084488","clinical_significance":[],"end":140559484,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140559484,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs2130570893","seq_region_name":"7","clinical_significance":[],"end":140559488,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140559488,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1797525225","seq_region_name":"7","clinical_significance":[],"start":140559490,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140559490,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1387471073","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559491,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140559491},{"id":"rs1370339214","seq_region_name":"7","clinical_significance":[],"end":140559492,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140559492,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140559493,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140559493,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797525722"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1324545834","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559494,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140559494},{"clinical_significance":[],"seq_region_name":"7","id":"rs908395838","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559496,"feature_type":"variation","strand":1,"end":140559496,"alleles":["C","A"]},{"start":140559497,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140559497,"alleles":["A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs914989543","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559498,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140559498,"seq_region_name":"7","id":"rs939852786","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797526402","clinical_significance":[],"strand":1,"feature_type":"variation","end":140559500,"alleles":["T","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559500,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559502,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","-"],"end":140559502,"seq_region_name":"7","id":"rs1159377487","clinical_significance":[]},{"seq_region_name":"7","id":"rs1041390133","clinical_significance":[],"alleles":["G","A"],"end":140559504,"strand":1,"feature_type":"variation","start":140559504,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140559508,"alleles":["GGG","GGGG"],"strand":1,"feature_type":"variation","start":140559506,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1797526781","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140559507,"alleles":["G","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559507,"clinical_significance":[],"seq_region_name":"7","id":"rs1361745549"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797527027","source":"dbSNP","start":140559508,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140559508,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1424719084","source":"dbSNP","start":140559510,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140559510,"alleles":["A","C"],"feature_type":"variation","strand":1},{"alleles":["C","T"],"end":140559514,"feature_type":"variation","strand":1,"source":"dbSNP","start":140559514,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs922537683","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559515,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140559515,"seq_region_name":"7","id":"rs529384075","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1367174990","source":"dbSNP","start":140559519,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140559519,"feature_type":"variation","strand":1},{"end":140559520,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140559520,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1254739232","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140559524,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559524,"clinical_significance":[],"seq_region_name":"7","id":"rs1191681810"},{"clinical_significance":[],"id":"rs1042228572","seq_region_name":"7","source":"dbSNP","start":140559526,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C","G"],"end":140559526,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["G","C","T"],"end":140559528,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559528,"source":"dbSNP","seq_region_name":"7","id":"rs1797528109","clinical_significance":[]},{"start":140559529,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140559529,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs772305771","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140559533,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559533,"clinical_significance":[],"seq_region_name":"7","id":"rs1797528352"},{"clinical_significance":[],"seq_region_name":"7","id":"rs547454283","source":"dbSNP","start":140559538,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140559538,"alleles":["T","C"],"feature_type":"variation","strand":1},{"start":140559539,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140559539,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585631478","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs565758301","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559546,"feature_type":"variation","strand":1,"end":140559546,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs939286277","alleles":["C","T"],"end":140559547,"feature_type":"variation","strand":1,"source":"dbSNP","start":140559547,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1056296447","clinical_significance":[],"end":140559552,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140559552,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1309234798","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140559554,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559554},{"seq_region_name":"7","id":"rs1797529056","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559558,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140559558},{"clinical_significance":[],"seq_region_name":"7","id":"rs1049753920","end":140559561,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140559561,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1797529280","clinical_significance":[],"end":140559563,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140559563,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140559566,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140559566,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1797529391","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1797529493","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559568,"feature_type":"variation","strand":1,"end":140559568,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797529599","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140559571,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559571},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559573,"source":"dbSNP","strand":1,"feature_type":"variation","end":140559573,"alleles":["T","C"],"seq_region_name":"7","id":"rs79270752","clinical_significance":[]},{"start":140559574,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140559574,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1260424428","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797530152","alleles":["G","A"],"end":140559575,"feature_type":"variation","strand":1,"source":"dbSNP","start":140559575,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559576,"source":"dbSNP","strand":1,"feature_type":"variation","end":140559576,"alleles":["G","A"],"seq_region_name":"7","id":"rs1012865575","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797530496","source":"dbSNP","start":140559577,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140559577,"alleles":["G","A"],"feature_type":"variation","strand":1},{"start":140559579,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140559581,"alleles":["AAA","AA"],"strand":1,"feature_type":"variation","id":"rs1234055446","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs760071628","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559590,"source":"dbSNP","strand":1,"feature_type":"variation","end":140559590,"alleles":["C","G","T"]},{"start":140559592,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140559592,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797530903","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797531063","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140559595,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559595,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140559597,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559597,"source":"dbSNP","seq_region_name":"7","id":"rs1440853710","clinical_significance":[]},{"id":"rs1797531401","seq_region_name":"7","clinical_significance":[],"start":140559602,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140559602,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["A","C","T"],"end":140559604,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559604,"clinical_significance":[],"seq_region_name":"7","id":"rs552061513"},{"alleles":["A","G"],"end":140559607,"feature_type":"variation","strand":1,"source":"dbSNP","start":140559607,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1322934452","seq_region_name":"7"},{"alleles":["C","T"],"end":140559608,"feature_type":"variation","strand":1,"source":"dbSNP","start":140559608,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1297784863"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1380174536","source":"dbSNP","start":140559610,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140559610,"alleles":["T","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs570292397","clinical_significance":[],"strand":1,"feature_type":"variation","end":140559613,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559613,"source":"dbSNP"},{"end":140559614,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140559614,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs768331575","clinical_significance":[]},{"end":140559619,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140559619,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs537745610","clinical_significance":[]},{"id":"rs1585631620","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140559620,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559620,"source":"dbSNP"},{"source":"dbSNP","start":140559622,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140559622,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797533104"},{"seq_region_name":"7","id":"rs1797533365","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559626,"source":"dbSNP","strand":1,"feature_type":"variation","end":140559626,"alleles":["T","A"]},{"seq_region_name":"7","id":"rs1466051495","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C","T"],"end":140559628,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559628,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1358548348","source":"dbSNP","start":140559628,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AT","-"],"end":140559629,"feature_type":"variation","strand":1},{"id":"rs1229016084","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559629,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140559629},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130571433","end":140559631,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140559631,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1276750282","seq_region_name":"7","clinical_significance":[],"start":140559633,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140559633,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"start":140559635,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140559635,"alleles":["C","A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs555710940","clinical_significance":[]},{"id":"rs1797534082","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559637,"source":"dbSNP","strand":1,"feature_type":"variation","end":140559637,"alleles":["G","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559641,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140559641,"clinical_significance":[],"seq_region_name":"7","id":"rs1453688908"},{"end":140559642,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140559642,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1797534183","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559650,"source":"dbSNP","strand":1,"feature_type":"variation","end":140559650,"alleles":["C","T"],"seq_region_name":"7","id":"rs773081416","clinical_significance":[]},{"start":140559651,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140559651,"strand":1,"feature_type":"variation","id":"rs1797534409","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs961813877","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559652,"feature_type":"variation","strand":1,"end":140559652,"alleles":["G","A"]},{"source":"dbSNP","start":140559653,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140559653,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1797534614","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559653,"feature_type":"variation","strand":1,"end":140559657,"alleles":["TCTCT","TCT"],"clinical_significance":[],"seq_region_name":"7","id":"rs1445138336"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559656,"feature_type":"variation","strand":1,"end":140559656,"alleles":["C","G"],"clinical_significance":[],"id":"rs891986179","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140559664,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559664,"source":"dbSNP","seq_region_name":"7","id":"rs1797534929","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs747975043","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559665,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140559665},{"id":"rs1029917816","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559672,"source":"dbSNP","strand":1,"feature_type":"variation","end":140559672,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1797535261","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559676,"source":"dbSNP","strand":1,"feature_type":"variation","end":140559676,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1448578166","clinical_significance":[],"end":140559678,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140559678,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140559680,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559680,"source":"dbSNP","seq_region_name":"7","id":"rs1201262992","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs567843788","source":"dbSNP","start":140559684,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140559684,"alleles":["C","G","T"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140559685,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559685,"clinical_significance":[],"seq_region_name":"7","id":"rs1377143244"},{"seq_region_name":"7","id":"rs535556306","clinical_significance":[],"end":140559687,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140559687,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1298654283","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140559690,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559690},{"alleles":["G","A","C"],"end":140559691,"strand":1,"feature_type":"variation","start":140559691,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs770327450","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs776228343","clinical_significance":[],"strand":1,"feature_type":"variation","end":140559693,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559693,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1274289562","clinical_significance":[],"alleles":["C","A"],"end":140559697,"strand":1,"feature_type":"variation","start":140559697,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["G","C"],"end":140559700,"strand":1,"feature_type":"variation","start":140559700,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_region_variant","id":"rs1443352266","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140559701,"consequence_type":"splice_region_variant","assembly_name":"GRCh38","end":140559701,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1225614138"},{"end":140559703,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140559703,"consequence_type":"splice_donor_5th_base_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs746335005"},{"id":"rs762777619","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140559704,"assembly_name":"GRCh38","consequence_type":"splice_donor_region_variant","start":140559704,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140559709,"alleles":["T","C"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559709,"clinical_significance":[],"seq_region_name":"7","id":"rs370574635"},{"seq_region_name":"7","id":"rs1585631856","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140559713,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140559713,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140559719,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140559719,"id":"rs763289733","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559720,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140559720,"clinical_significance":[],"seq_region_name":"7","id":"rs1182401307"},{"source":"dbSNP","start":140559722,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","end":140559722,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs370159867"},{"seq_region_name":"7","id":"rs376031293","clinical_significance":[],"end":140559725,"alleles":["A","CT"],"strand":1,"feature_type":"variation","start":140559725,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"frameshift_variant"},{"source":"dbSNP","start":140559726,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140559726,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1310515850","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140559731,"alleles":["C","T"],"consequence_type":"stop_gained","assembly_name":"GRCh38","source":"dbSNP","start":140559731,"clinical_significance":[],"id":"rs1797537860","seq_region_name":"7"},{"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559734,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140559734,"clinical_significance":[],"id":"rs1390430489","seq_region_name":"7"},{"id":"rs547058088","seq_region_name":"7","clinical_significance":[],"start":140559736,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["C","T"],"end":140559736,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797538442","source":"dbSNP","start":140559739,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140559739,"alleles":["T","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs199689388","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140559740,"source":"dbSNP","strand":1,"feature_type":"variation","end":140559740,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs967844138","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140559741,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559741},{"seq_region_name":"7","id":"rs774402271","clinical_significance":[],"strand":1,"feature_type":"variation","end":140559743,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140559743,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1414811636","clinical_significance":[],"alleles":["C","T"],"end":140559745,"strand":1,"feature_type":"variation","start":140559745,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"alleles":["G","A"],"end":140559746,"feature_type":"variation","strand":1,"source":"dbSNP","start":140559746,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs375700667"},{"source":"dbSNP","start":140559750,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140559750,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs978218174"},{"seq_region_name":"7","id":"rs1357324299","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140559754,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140559754},{"start":140559755,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","end":140559755,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs767442888","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1474272778","clinical_significance":[],"alleles":["A","G"],"end":140559756,"strand":1,"feature_type":"variation","start":140559756,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"seq_region_name":"7","id":"rs1797539880","clinical_significance":[],"start":140559762,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140559762,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140559763,"alleles":["G","T"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559763,"clinical_significance":[],"seq_region_name":"7","id":"rs1797540001"},{"source":"dbSNP","start":140559766,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["T","C","G"],"end":140559766,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs750538500"},{"strand":1,"feature_type":"variation","end":140559767,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140559767,"source":"dbSNP","id":"rs1797540294","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs765255553","source":"dbSNP","start":140559768,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140559768,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140559776,"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140559776,"source":"dbSNP","seq_region_name":"7","id":"rs752752647","clinical_significance":[]},{"alleles":["TT","T"],"end":140559777,"strand":1,"feature_type":"variation","start":140559776,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"frameshift_variant","seq_region_name":"7","id":"rs1367635593","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1269817209","consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559785,"feature_type":"variation","strand":1,"end":140559785,"alleles":["A","C"]},{"id":"rs758236900","seq_region_name":"7","clinical_significance":[],"start":140559787,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140559787,"alleles":["C","A","G"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140559790,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140559790,"seq_region_name":"7","id":"rs1221268986","clinical_significance":[]},{"clinical_significance":[],"id":"rs1277158726","seq_region_name":"7","end":140559794,"alleles":["C","A","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140559794,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559799,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140559799,"clinical_significance":[],"seq_region_name":"7","id":"rs1797541513"},{"feature_type":"variation","strand":1,"end":140559800,"alleles":["C","T"],"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559800,"clinical_significance":[],"seq_region_name":"7","id":"rs777673496"},{"seq_region_name":"7","id":"rs1202500144","clinical_significance":[],"end":140559806,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140559806,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs746595174","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559807,"feature_type":"variation","strand":1,"end":140559807,"alleles":["G","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585632198","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559808,"feature_type":"variation","strand":1,"end":140559808,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs1797542154","clinical_significance":[],"strand":1,"feature_type":"variation","end":140559810,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140559810,"source":"dbSNP"},{"alleles":["C","T"],"end":140559815,"strand":1,"feature_type":"variation","start":140559815,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_region_variant","seq_region_name":"7","id":"rs1476293198","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs553872704","consequence_type":"splice_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559817,"feature_type":"variation","strand":1,"end":140559817,"alleles":["A","G"]},{"end":140559818,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140559818,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_acceptor_variant","seq_region_name":"7","id":"rs1186344006","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"splice_region_variant","start":140559820,"source":"dbSNP","strand":1,"feature_type":"variation","end":140559820,"alleles":["G","T"],"id":"rs1372121069","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"splice_polypyrimidine_tract_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559830,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140559830,"clinical_significance":[],"seq_region_name":"7","id":"rs759205075"},{"assembly_name":"GRCh38","consequence_type":"splice_polypyrimidine_tract_variant","start":140559831,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140559831,"seq_region_name":"7","id":"rs1554468168","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs745393828","consequence_type":"splice_polypyrimidine_tract_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559832,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140559832},{"seq_region_name":"7","id":"rs1422997275","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140559834,"assembly_name":"GRCh38","consequence_type":"splice_polypyrimidine_tract_variant","start":140559834,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140559838,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559838,"source":"dbSNP","seq_region_name":"7","id":"rs923824353","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140559844,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559844,"source":"dbSNP","seq_region_name":"7","id":"rs1469174024","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559845,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140559845,"clinical_significance":[],"seq_region_name":"7","id":"rs370134241"},{"clinical_significance":[],"id":"rs374621400","seq_region_name":"7","source":"dbSNP","start":140559846,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140559846,"feature_type":"variation","strand":1},{"id":"rs1432968457","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140559848,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559848,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559850,"source":"dbSNP","strand":1,"feature_type":"variation","end":140559850,"alleles":["A","C"],"seq_region_name":"7","id":"rs1317958555","clinical_significance":[]},{"start":140559855,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140559855,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs1285119263","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs976611704","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559856,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140559856},{"alleles":["C","A"],"end":140559858,"strand":1,"feature_type":"variation","start":140559858,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1331860085","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563141302","source":"dbSNP","start":140559863,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A","C"],"end":140559863,"feature_type":"variation","strand":1},{"end":140559868,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140559868,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130572179"},{"start":140559869,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140559869,"alleles":["A","G"],"strand":1,"feature_type":"variation","id":"rs1056345490","seq_region_name":"7","clinical_significance":[]},{"id":"rs1797544510","seq_region_name":"7","clinical_significance":[],"end":140559870,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140559870,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["C","T"],"end":140559876,"feature_type":"variation","strand":1,"source":"dbSNP","start":140559876,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs916488050","seq_region_name":"7"},{"source":"dbSNP","start":140559877,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140559877,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs922389877"},{"source":"dbSNP","start":140559879,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140559879,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs947938644"},{"clinical_significance":[],"seq_region_name":"7","id":"rs932593591","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140559895,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559895},{"seq_region_name":"7","id":"rs1797544989","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140559899,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559899,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1797545108","seq_region_name":"7","feature_type":"variation","strand":1,"end":140559909,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559909},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797545206","end":140559913,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140559913,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1797545310","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140559918,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559918,"source":"dbSNP"},{"start":140559922,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140559922,"alleles":["T","G"],"strand":1,"feature_type":"variation","id":"rs767280446","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","G","T"],"end":140559925,"strand":1,"feature_type":"variation","start":140559925,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs142592854","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140559926,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559926,"source":"dbSNP","seq_region_name":"7","id":"rs1408171421","clinical_significance":[]},{"source":"dbSNP","start":140559929,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140559929,"alleles":["T","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1005647154"},{"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140559930,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559930,"source":"dbSNP","seq_region_name":"7","id":"rs1395738397","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797546251","clinical_significance":[],"start":140559932,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140559932,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140559937,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559937,"source":"dbSNP","seq_region_name":"7","id":"rs1435575805","clinical_significance":[]},{"id":"rs1299677621","seq_region_name":"7","clinical_significance":[],"start":140559941,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140559941,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"end":140559943,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140559943,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797546642","clinical_significance":[]},{"source":"dbSNP","start":140559949,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140559949,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1554468184","seq_region_name":"7"},{"start":140559950,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140559950,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797546991","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559951,"source":"dbSNP","strand":1,"feature_type":"variation","end":140559951,"alleles":["G","C"],"id":"rs1797547136","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140559952,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140559952,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs2130572352","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1797547300","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559956,"source":"dbSNP","strand":1,"feature_type":"variation","end":140559956,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1476098643","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140559959,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559959,"source":"dbSNP"},{"end":140559962,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140559962,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1415868296","clinical_significance":[]},{"alleles":["G","C"],"end":140559963,"strand":1,"feature_type":"variation","start":140559963,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797547796","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140559965,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559965,"clinical_significance":[],"seq_region_name":"7","id":"rs557733540"},{"id":"rs1362946647","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140559966,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559966,"source":"dbSNP"},{"end":140559967,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140559967,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797548318","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140559968,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559968,"clinical_significance":[],"seq_region_name":"7","id":"rs1797548494"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1234702935","source":"dbSNP","start":140559971,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140559971,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1213414215","seq_region_name":"7","alleles":["G","A"],"end":140559972,"feature_type":"variation","strand":1,"source":"dbSNP","start":140559972,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1797548874","clinical_significance":[],"strand":1,"feature_type":"variation","end":140559978,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559978,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1437732494","feature_type":"variation","strand":1,"end":140559979,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559979},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585632570","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559980,"feature_type":"variation","strand":1,"end":140559980,"alleles":["C","T"]},{"clinical_significance":[],"id":"rs925972975","seq_region_name":"7","end":140559985,"alleles":["CCCCCC","CCCCC","CCCCCCC"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140559980,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs764636820","feature_type":"variation","strand":1,"end":140559984,"alleles":["C","A","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559984},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797549522","feature_type":"variation","strand":1,"end":140559990,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559990},{"seq_region_name":"7","id":"rs576289320","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140559991,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140559991},{"clinical_significance":[],"seq_region_name":"7","id":"rs550417552","feature_type":"variation","strand":1,"end":140559992,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140559992},{"alleles":["A","G"],"end":140559998,"feature_type":"variation","strand":1,"source":"dbSNP","start":140559998,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs543689492"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1029802087","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560001,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140560001},{"seq_region_name":"7","id":"rs775048318","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560002,"source":"dbSNP","strand":1,"feature_type":"variation","end":140560002,"alleles":["T","C"]},{"id":"rs1797550244","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560006,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140560006},{"alleles":["C","T"],"end":140560007,"feature_type":"variation","strand":1,"source":"dbSNP","start":140560007,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1439456552"},{"feature_type":"variation","strand":1,"end":140560010,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560010,"clinical_significance":[],"seq_region_name":"7","id":"rs1797550459"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140560012,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560012,"clinical_significance":[],"seq_region_name":"7","id":"rs1797550550"},{"seq_region_name":"7","id":"rs1045900359","clinical_significance":[],"end":140560013,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140560013,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140560015,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140560015,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797550786"},{"clinical_significance":[],"id":"rs890045987","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560019,"feature_type":"variation","strand":1,"end":140560019,"alleles":["T","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs905999770","end":140560025,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140560025,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140560027,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140560027,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797551105","clinical_significance":[]},{"source":"dbSNP","start":140560053,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140560053,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1392048871"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797551319","feature_type":"variation","strand":1,"end":140560054,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560054},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560059,"source":"dbSNP","strand":1,"feature_type":"variation","end":140560059,"alleles":["A","G"],"seq_region_name":"7","id":"rs1164429692","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797551560","end":140560060,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140560060,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1461109856","clinical_significance":[],"alleles":["C","T"],"end":140560062,"strand":1,"feature_type":"variation","start":140560062,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560065,"feature_type":"variation","strand":1,"end":140560065,"alleles":["G","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1007532896"},{"seq_region_name":"7","id":"rs1189618410","clinical_significance":[],"start":140560067,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140560067,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1797552016","seq_region_name":"7","source":"dbSNP","start":140560068,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140560068,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1457936422","clinical_significance":[],"end":140560070,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140560070,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1001814137","alleles":["A","G"],"end":140560073,"feature_type":"variation","strand":1,"source":"dbSNP","start":140560073,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1797552235","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140560074,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560074,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs568487330","feature_type":"variation","strand":1,"end":140560077,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560077},{"alleles":["A","C"],"end":140560080,"feature_type":"variation","strand":1,"source":"dbSNP","start":140560080,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797552453"},{"clinical_significance":[],"id":"rs1797552552","seq_region_name":"7","alleles":["A","G"],"end":140560081,"feature_type":"variation","strand":1,"source":"dbSNP","start":140560081,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs11975074","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560087,"feature_type":"variation","strand":1,"end":140560087,"alleles":["T","A","C"]},{"strand":1,"feature_type":"variation","end":140560088,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560088,"source":"dbSNP","id":"rs1797552856","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797552968","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560090,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140560090},{"start":140560092,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140560092,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797553064","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560096,"feature_type":"variation","strand":1,"alleles":["-","A"],"end":140560095,"clinical_significance":[],"id":"rs1797553171","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560096,"source":"dbSNP","strand":1,"feature_type":"variation","end":140560096,"alleles":["T","A","C"],"seq_region_name":"7","id":"rs1474706401","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["AAAAAAA","AAAAAAAA"],"end":140560103,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560097,"source":"dbSNP","seq_region_name":"7","id":"rs1247729746","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797553526","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560104,"feature_type":"variation","strand":1,"end":140560103,"alleles":["-","T"]},{"clinical_significance":[],"id":"rs768256307","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560104,"feature_type":"variation","strand":1,"end":140560104,"alleles":["C","G","T"]},{"seq_region_name":"7","id":"rs541130709","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140560105,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560105,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560111,"feature_type":"variation","strand":1,"end":140560111,"alleles":["C","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1797553850"},{"seq_region_name":"7","id":"rs1797553963","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560113,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140560113},{"clinical_significance":[],"id":"rs1797554071","seq_region_name":"7","source":"dbSNP","start":140560120,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140560121,"alleles":["CC","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs952387855","source":"dbSNP","start":140560124,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140560124,"alleles":["A","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1797554291","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["GGAGGCTCAGGAATCTGGAAGGC","GGAGGCTCAGGAATCTGGAAGGCGGAGGCTCAGGAATCTGGAAGGC"],"end":140560149,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560127,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140560130,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560130,"clinical_significance":[],"seq_region_name":"7","id":"rs1585632844"},{"seq_region_name":"7","id":"rs960559862","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560131,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140560131},{"seq_region_name":"7","id":"rs1467383235","clinical_significance":[],"alleles":["C","G"],"end":140560132,"strand":1,"feature_type":"variation","start":140560132,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560136,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140560136,"seq_region_name":"7","id":"rs1005215310","clinical_significance":[]},{"clinical_significance":[],"id":"rs1797554880","seq_region_name":"7","source":"dbSNP","start":140560137,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140560137,"alleles":["G","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1797554980","seq_region_name":"7","source":"dbSNP","start":140560141,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140560141,"alleles":["C","T"],"feature_type":"variation","strand":1},{"start":140560147,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140560147,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797555138","clinical_significance":[]},{"seq_region_name":"7","id":"rs1416295534","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560153,"source":"dbSNP","strand":1,"feature_type":"variation","end":140560153,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs2130572875","clinical_significance":[],"strand":1,"feature_type":"variation","end":140560153,"alleles":["G","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560153,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560154,"source":"dbSNP","strand":1,"feature_type":"variation","end":140560154,"alleles":["C","A"],"seq_region_name":"7","id":"rs1317117070","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140560158,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560158,"source":"dbSNP","seq_region_name":"7","id":"rs2130572894","clinical_significance":[]},{"id":"rs1015391782","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560159,"source":"dbSNP","strand":1,"feature_type":"variation","end":140560159,"alleles":["A","C","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560165,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140560165,"clinical_significance":[],"seq_region_name":"7","id":"rs1797555778"},{"strand":1,"feature_type":"variation","end":140560167,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560167,"source":"dbSNP","seq_region_name":"7","id":"rs1797555946","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797556109","source":"dbSNP","start":140560169,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140560169,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs146489468","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140560173,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560173},{"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140560192,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560192,"clinical_significance":[],"seq_region_name":"7","id":"rs1405670091"},{"alleles":["C","T"],"end":140560193,"strand":1,"feature_type":"variation","start":140560193,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1797556684","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1304005473","clinical_significance":[],"end":140560194,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140560194,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560198,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140560198,"seq_region_name":"7","id":"rs1585632938","clinical_significance":[]},{"alleles":["T","C"],"end":140560200,"feature_type":"variation","strand":1,"source":"dbSNP","start":140560200,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1443051733"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560203,"feature_type":"variation","strand":1,"end":140560203,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs533243017"},{"clinical_significance":[],"seq_region_name":"7","id":"rs916375519","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560204,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140560204},{"feature_type":"variation","strand":1,"end":140560210,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560210,"clinical_significance":[],"seq_region_name":"7","id":"rs947990933"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560211,"source":"dbSNP","strand":1,"feature_type":"variation","end":140560211,"alleles":["A","G"],"seq_region_name":"7","id":"rs1435614399","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs779202773","feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140560213,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560213},{"id":"rs1400136083","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140560214,"alleles":["C","A","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560214,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1797558395","clinical_significance":[],"strand":1,"feature_type":"variation","end":140560215,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560215,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797558539","feature_type":"variation","strand":1,"end":140560220,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560220},{"seq_region_name":"7","id":"rs2130573059","clinical_significance":[],"end":140560222,"alleles":["G","-"],"strand":1,"feature_type":"variation","start":140560222,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797558702","source":"dbSNP","start":140560223,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140560223,"alleles":["T","C"],"feature_type":"variation","strand":1},{"end":140560326,"alleles":["ACATTCTCAGTGAATAAATCCAGTAAAACCATATTATGCTGGGAAATTCAACTAATTTCAGACAGTCATTGAGTGTTGGAACTAGAAGGAAGCGTGACA","ACA"],"strand":1,"feature_type":"variation","start":140560228,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797558850","clinical_significance":[]},{"end":140560229,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140560229,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1176037085","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs141105675","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560230,"feature_type":"variation","strand":1,"end":140560230,"alleles":["A","G"]},{"end":140560232,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140560232,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797559379"},{"clinical_significance":[],"seq_region_name":"7","id":"rs941356224","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140560233,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560233},{"seq_region_name":"7","id":"rs1797559706","clinical_significance":[],"end":140560235,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140560235,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560236,"feature_type":"variation","strand":1,"alleles":["A","-"],"end":140560236,"clinical_significance":[],"seq_region_name":"7","id":"rs1189599721"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797559848","source":"dbSNP","start":140560236,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140560236,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560239,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140560239,"clinical_significance":[],"seq_region_name":"7","id":"rs143532753"},{"source":"dbSNP","start":140560241,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140560241,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1487093152"},{"source":"dbSNP","start":140560248,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140560248,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797560483"},{"seq_region_name":"7","id":"rs1797560650","clinical_significance":[],"start":140560253,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140560253,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140560258,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560258,"source":"dbSNP","seq_region_name":"7","id":"rs1243422646","clinical_significance":[]},{"id":"rs146780895","seq_region_name":"7","clinical_significance":[],"start":140560259,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140560259,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140560264,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560264,"clinical_significance":[],"seq_region_name":"7","id":"rs377596674"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560277,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140560277,"id":"rs936035582","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797561474","source":"dbSNP","start":140560280,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140560280,"alleles":["T","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797561647","feature_type":"variation","strand":1,"end":140560292,"alleles":["CAGACAG","CAG"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560286},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560290,"feature_type":"variation","strand":1,"end":140560290,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1797561814"},{"strand":1,"feature_type":"variation","end":140560298,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560298,"source":"dbSNP","seq_region_name":"7","id":"rs751193048","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797562169","source":"dbSNP","start":140560299,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140560299,"alleles":["A","G"],"feature_type":"variation","strand":1},{"start":140560302,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140560302,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1345621137","clinical_significance":[]},{"seq_region_name":"7","id":"rs1216989641","clinical_significance":[],"start":140560303,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140560303,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140560312,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560312,"clinical_significance":[],"id":"rs1282198728","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140560316,"alleles":["G","C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560316,"source":"dbSNP","id":"rs897252636","seq_region_name":"7","clinical_significance":[]},{"end":140560323,"alleles":["GCGTG","GCGTGCGTG"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140560319,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797562974"},{"clinical_significance":[],"seq_region_name":"7","id":"rs564467437","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560320,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140560320},{"start":140560321,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140560321,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs988768127","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797563365","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560322,"feature_type":"variation","strand":1,"end":140560330,"alleles":["TGACACCAT","TGACACCATTCAGCCTGACACCAT"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560327,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140560327,"clinical_significance":[],"id":"rs1287286576","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1051287339","clinical_significance":[],"alleles":["C","A"],"end":140560328,"strand":1,"feature_type":"variation","start":140560328,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1797563578","clinical_significance":[],"start":140560330,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140560330,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797563683","end":140560332,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140560332,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs528636043","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560335,"feature_type":"variation","strand":1,"end":140560335,"alleles":["C","T"]},{"strand":1,"feature_type":"variation","end":140560338,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560338,"source":"dbSNP","seq_region_name":"7","id":"rs1797563894","clinical_significance":[]},{"start":140560340,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140560340,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797563999","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1007172934","alleles":["G","A","T"],"end":140560353,"feature_type":"variation","strand":1,"source":"dbSNP","start":140560353,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560354,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140560354,"clinical_significance":[],"seq_region_name":"7","id":"rs140463984"},{"end":140560360,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140560360,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1314808859","clinical_significance":[]},{"seq_region_name":"7","id":"rs1433005682","clinical_significance":[],"end":140560365,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140560365,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140560366,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140560366,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs903556284","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1797564659","seq_region_name":"7","source":"dbSNP","start":140560368,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140560368,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560370,"source":"dbSNP","strand":1,"feature_type":"variation","end":140560370,"alleles":["C","T"],"seq_region_name":"7","id":"rs547522091","clinical_significance":[]},{"seq_region_name":"7","id":"rs535810793","clinical_significance":[],"strand":1,"feature_type":"variation","end":140560372,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560372,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs960445872","source":"dbSNP","start":140560373,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140560373,"feature_type":"variation","strand":1},{"start":140560375,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140560376,"alleles":["GG","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1049375910","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130573387","end":140560376,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140560376,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797565267","alleles":["A","T"],"end":140560381,"feature_type":"variation","strand":1,"source":"dbSNP","start":140560381,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560383,"feature_type":"variation","strand":1,"end":140560383,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130573399"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560390,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140560390,"seq_region_name":"7","id":"rs1474864169","clinical_significance":[]},{"id":"rs1797565500","seq_region_name":"7","clinical_significance":[],"alleles":["T","A"],"end":140560391,"strand":1,"feature_type":"variation","start":140560391,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs991846718","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140560392,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560392},{"clinical_significance":[],"id":"rs2130573424","seq_region_name":"7","end":140560394,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140560394,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1797565681","seq_region_name":"7","clinical_significance":[],"alleles":["T","G"],"end":140560397,"strand":1,"feature_type":"variation","start":140560397,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["A","C","G"],"end":140560401,"feature_type":"variation","strand":1,"source":"dbSNP","start":140560401,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs767407219","seq_region_name":"7"},{"alleles":["T","A"],"end":140560402,"strand":1,"feature_type":"variation","start":140560402,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1585633382","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140560403,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560403,"clinical_significance":[],"id":"rs1197364898","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560404,"feature_type":"variation","strand":1,"end":140560404,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1797566124"},{"seq_region_name":"7","id":"rs1212395373","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560405,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140560405},{"seq_region_name":"7","id":"rs13238072","clinical_significance":[],"start":140560406,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140560406,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140560411,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140560411,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797566438"},{"start":140560412,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140560412,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1023436413","clinical_significance":[]},{"clinical_significance":[],"id":"rs1428783425","seq_region_name":"7","source":"dbSNP","start":140560419,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140560419,"feature_type":"variation","strand":1},{"start":140560431,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140560431,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130573503","clinical_significance":[]},{"start":140560432,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140560432,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1473032019","clinical_significance":[]},{"end":140560434,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140560434,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1279443991","seq_region_name":"7"},{"id":"rs758551197","seq_region_name":"7","clinical_significance":[],"end":140560438,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140560438,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs969179689","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560440,"source":"dbSNP","strand":1,"feature_type":"variation","end":140560440,"alleles":["T","A"]},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140560442,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560442,"source":"dbSNP","seq_region_name":"7","id":"rs984765571","clinical_significance":[]},{"source":"dbSNP","start":140560442,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140560448,"alleles":["TTTTTTT","TTTTTT"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130573549"},{"clinical_significance":[],"id":"rs1205167890","seq_region_name":"7","source":"dbSNP","start":140560446,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140560446,"alleles":["T","C"],"feature_type":"variation","strand":1},{"id":"rs1797567446","seq_region_name":"7","clinical_significance":[],"start":140560450,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140560450,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs140646476","clinical_significance":[],"strand":1,"feature_type":"variation","end":140560463,"alleles":["CTCTCTCTCTCTCT","CTCTCTCTCT","CTCTCTCTCTCT","CTCTCTCTCTCTCTCT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560450,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1293139839","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560461,"feature_type":"variation","strand":1,"alleles":["TCTTT","T"],"end":140560465},{"seq_region_name":"7","id":"rs1213828174","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140560462,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560462,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140560463,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560463,"clinical_significance":[],"seq_region_name":"7","id":"rs1295422493"},{"seq_region_name":"7","id":"rs1356322600","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560463,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TTT","T"],"end":140560465},{"alleles":["T","C"],"end":140560464,"strand":1,"feature_type":"variation","start":140560464,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs909115116","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560468,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140560468,"clinical_significance":[],"seq_region_name":"7","id":"rs1374941248"},{"alleles":["A","C","G"],"end":140560469,"feature_type":"variation","strand":1,"source":"dbSNP","start":140560469,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs181734096"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797568727","source":"dbSNP","start":140560471,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140560471,"alleles":["A","G"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560473,"source":"dbSNP","strand":1,"feature_type":"variation","end":140560473,"alleles":["T","A"],"seq_region_name":"7","id":"rs557505032","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130573668","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560474,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140560474},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560478,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140560478,"seq_region_name":"7","id":"rs1585633576","clinical_significance":[]},{"seq_region_name":"7","id":"rs187375272","clinical_significance":[],"strand":1,"feature_type":"variation","end":140560485,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560485,"source":"dbSNP"},{"seq_region_name":"7","id":"rs150408235","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140560488,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560488,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560491,"source":"dbSNP","strand":1,"feature_type":"variation","end":140560491,"alleles":["A","T"],"seq_region_name":"7","id":"rs1797569303","clinical_significance":[]},{"clinical_significance":[],"id":"rs1462352917","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140560493,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560493},{"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140560497,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560497,"source":"dbSNP","seq_region_name":"7","id":"rs1418040654","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1029807549","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140560499,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560499},{"seq_region_name":"7","id":"rs1797569788","clinical_significance":[],"end":140560500,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140560500,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560502,"source":"dbSNP","strand":1,"feature_type":"variation","end":140560502,"alleles":["C","T"],"seq_region_name":"7","id":"rs1797569899","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140560510,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560510,"clinical_significance":[],"id":"rs1402493314","seq_region_name":"7"},{"end":140560524,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140560524,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1177319492","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797570227","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560525,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140560525},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797570625","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560532,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140560532},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130573782","source":"dbSNP","start":140560534,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140560534,"feature_type":"variation","strand":1},{"id":"rs191204223","seq_region_name":"7","clinical_significance":[],"alleles":["G","C"],"end":140560537,"strand":1,"feature_type":"variation","start":140560537,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140560541,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560541,"source":"dbSNP","seq_region_name":"7","id":"rs1797571003","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797571143","clinical_significance":[],"strand":1,"feature_type":"variation","end":140560543,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560543,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585633676","source":"dbSNP","start":140560544,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140560544,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1051170009","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560550,"feature_type":"variation","strand":1,"end":140560550,"alleles":["G","A","T"]},{"clinical_significance":[],"id":"rs1797571496","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560551,"feature_type":"variation","strand":1,"end":140560551,"alleles":["G","T"]},{"feature_type":"variation","strand":1,"end":140560559,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560559,"clinical_significance":[],"seq_region_name":"7","id":"rs1585633699"},{"clinical_significance":[],"seq_region_name":"7","id":"rs953931457","end":140560560,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140560560,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1797571824","clinical_significance":[],"strand":1,"feature_type":"variation","end":140560561,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560561,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1335241252","alleles":["T","A"],"end":140560562,"feature_type":"variation","strand":1,"source":"dbSNP","start":140560562,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1797572016","seq_region_name":"7","source":"dbSNP","start":140560564,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["GG","G"],"end":140560565,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1275220513","clinical_significance":[],"alleles":["G","A"],"end":140560568,"strand":1,"feature_type":"variation","start":140560568,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["T","A"],"end":140560570,"feature_type":"variation","strand":1,"source":"dbSNP","start":140560570,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs985250846","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1350647647","source":"dbSNP","start":140560572,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140560572,"alleles":["A","C","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1355108798","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560573,"feature_type":"variation","strand":1,"end":140560573,"alleles":["C","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130573912","end":140560578,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140560578,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["G","A"],"end":140560579,"feature_type":"variation","strand":1,"source":"dbSNP","start":140560579,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1307767076"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1393272629","feature_type":"variation","strand":1,"end":140560589,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560589},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797572875","feature_type":"variation","strand":1,"end":140560595,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560595},{"seq_region_name":"7","id":"rs1797572955","clinical_significance":[],"end":140560602,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140560602,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1371804103","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560619,"feature_type":"variation","strand":1,"end":140560619,"alleles":["C","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560620,"feature_type":"variation","strand":1,"end":140560620,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1298106184"},{"end":140560621,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140560621,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1442019095"},{"seq_region_name":"7","id":"rs1797573385","clinical_significance":[],"start":140560622,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140560622,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560623,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140560623,"clinical_significance":[],"id":"rs1797573500","seq_region_name":"7"},{"end":140560624,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140560624,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1229816739","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560625,"feature_type":"variation","strand":1,"end":140560625,"alleles":["C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1797573732"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560626,"feature_type":"variation","strand":1,"end":140560626,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1032928988"},{"source":"dbSNP","start":140560628,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140560628,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130574055"},{"end":140560629,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140560629,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1166601245"},{"id":"rs180830537","seq_region_name":"7","clinical_significance":[],"start":140560632,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140560632,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs957286067","source":"dbSNP","start":140560632,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140560642,"alleles":["AAAAAAAAAAA","AAAAAAAAAA","AAAAAAAAAAAA"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs547072969","clinical_significance":[],"end":140560634,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140560634,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140560637,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140560637,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797574494"},{"source":"dbSNP","start":140560642,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140560642,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs74892174"},{"clinical_significance":[],"seq_region_name":"7","id":"rs77901819","source":"dbSNP","start":140560643,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140560643,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs950077853","alleles":["A","G","T"],"end":140560647,"feature_type":"variation","strand":1,"source":"dbSNP","start":140560647,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs2130574135","seq_region_name":"7","source":"dbSNP","start":140560648,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140560648,"feature_type":"variation","strand":1},{"id":"rs556948284","seq_region_name":"7","clinical_significance":[],"start":140560653,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140560653,"strand":1,"feature_type":"variation"},{"alleles":["G","A"],"end":140560654,"feature_type":"variation","strand":1,"source":"dbSNP","start":140560654,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1044015058"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560654,"feature_type":"variation","strand":1,"alleles":["GGG","GG"],"end":140560656,"clinical_significance":[],"seq_region_name":"7","id":"rs1797575138"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560656,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140560656,"clinical_significance":[],"seq_region_name":"7","id":"rs578054447"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560659,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140560659,"seq_region_name":"7","id":"rs1585633887","clinical_significance":[]},{"id":"rs1585633901","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140560662,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560662,"source":"dbSNP"},{"source":"dbSNP","start":140560666,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140560666,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585633907"},{"seq_region_name":"7","id":"rs1291136962","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560667,"source":"dbSNP","strand":1,"feature_type":"variation","end":140560667,"alleles":["C","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560668,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140560668,"clinical_significance":[],"seq_region_name":"7","id":"rs1585633923"},{"clinical_significance":[],"id":"rs1797575882","seq_region_name":"7","feature_type":"variation","strand":1,"end":140560669,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560669},{"clinical_significance":[],"seq_region_name":"7","id":"rs927363808","source":"dbSNP","start":140560671,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140560671,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs904109155","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560672,"feature_type":"variation","strand":1,"end":140560672,"alleles":["C","G","T"]},{"source":"dbSNP","start":140560674,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140560674,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1211639584"},{"seq_region_name":"7","id":"rs1334422965","clinical_significance":[],"start":140560679,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140560679,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"end":140560680,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140560680,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797576483","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560681,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140560681,"seq_region_name":"7","id":"rs1797576580","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797576666","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560684,"source":"dbSNP","strand":1,"feature_type":"variation","end":140560684,"alleles":["C","G"]},{"id":"rs999741617","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140560686,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560686,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1261601754","clinical_significance":[],"alleles":["A","G"],"end":140560694,"strand":1,"feature_type":"variation","start":140560694,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560695,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140560695,"id":"rs1585634006","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797577045","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560697,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140560697},{"start":140560698,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140560698,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797577140","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140560699,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560699,"source":"dbSNP","id":"rs1797577215","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1585634013","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560701,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140560701},{"start":140560702,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140560702,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797577414","clinical_significance":[]},{"seq_region_name":"7","id":"rs545467565","clinical_significance":[],"start":140560703,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140560703,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1797577602","clinical_significance":[],"strand":1,"feature_type":"variation","end":140560704,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560704,"source":"dbSNP"},{"alleles":["G","T"],"end":140560705,"feature_type":"variation","strand":1,"source":"dbSNP","start":140560705,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1241186422"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560708,"source":"dbSNP","strand":1,"feature_type":"variation","end":140560708,"alleles":["A","G"],"seq_region_name":"7","id":"rs1797577821","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560709,"source":"dbSNP","strand":1,"feature_type":"variation","end":140560709,"alleles":["A","G"],"seq_region_name":"7","id":"rs750452625","clinical_significance":[]},{"source":"dbSNP","start":140560710,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140560710,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1797578049","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797578146","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560713,"feature_type":"variation","strand":1,"end":140560713,"alleles":["C","T"]},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140560716,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560716,"source":"dbSNP","seq_region_name":"7","id":"rs1797578253","clinical_significance":[]},{"clinical_significance":[],"id":"rs1797578337","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560717,"feature_type":"variation","strand":1,"end":140560717,"alleles":["G","A"]},{"id":"rs1052068521","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560718,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140560718},{"start":140560720,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","-"],"end":140560720,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1306848181","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140560723,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560723,"source":"dbSNP","seq_region_name":"7","id":"rs2130574396","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560723,"feature_type":"variation","strand":1,"alleles":["GG","G"],"end":140560724,"clinical_significance":[],"seq_region_name":"7","id":"rs1563141799"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560726,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140560726,"clinical_significance":[],"seq_region_name":"7","id":"rs1235706080"},{"source":"dbSNP","start":140560731,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140560731,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs868500058","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1373885110","clinical_significance":[],"strand":1,"feature_type":"variation","end":140560732,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560732,"source":"dbSNP"},{"seq_region_name":"7","id":"rs896126803","clinical_significance":[],"end":140560740,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140560740,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140560747,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140560747,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1013316362"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140560748,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560748,"clinical_significance":[],"seq_region_name":"7","id":"rs887912380"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1829769","feature_type":"variation","strand":1,"end":140560752,"alleles":["G","A","C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560752},{"clinical_significance":[],"id":"rs1157569597","seq_region_name":"7","feature_type":"variation","strand":1,"end":140560753,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560753},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560757,"feature_type":"variation","strand":1,"end":140560757,"alleles":["C","A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1797579721"},{"strand":1,"feature_type":"variation","end":140560760,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560760,"source":"dbSNP","seq_region_name":"7","id":"rs530903864","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560761,"feature_type":"variation","strand":1,"end":140560761,"alleles":["G","A"],"clinical_significance":[],"id":"rs551531755","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1797580079","clinical_significance":[],"start":140560765,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140560765,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"start":140560778,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140560784,"alleles":["AAAAAAA","AAAAAA","AAAAAAAA"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797580176","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140560782,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560782,"source":"dbSNP","seq_region_name":"7","id":"rs1191510560","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560791,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140560791,"id":"rs896842054","seq_region_name":"7","clinical_significance":[]},{"id":"rs1797580557","seq_region_name":"7","clinical_significance":[],"start":140560793,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140560793,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560794,"source":"dbSNP","strand":1,"feature_type":"variation","end":140560794,"alleles":["T","C"],"seq_region_name":"7","id":"rs561522219","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140560795,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560795,"clinical_significance":[],"seq_region_name":"7","id":"rs1797580798"},{"end":140560802,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140560802,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585634211"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560803,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","G","T"],"end":140560803,"seq_region_name":"7","id":"rs1829768","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585634250","feature_type":"variation","strand":1,"end":140560806,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560806},{"alleles":["T","C"],"end":140560810,"feature_type":"variation","strand":1,"source":"dbSNP","start":140560810,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1260190389"},{"seq_region_name":"7","id":"rs1163625738","clinical_significance":[],"end":140560813,"alleles":["TGTA","-"],"strand":1,"feature_type":"variation","start":140560810,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1797581606","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560811,"feature_type":"variation","strand":1,"end":140560811,"alleles":["G","A"]},{"alleles":["-","CCT"],"end":140560819,"strand":1,"feature_type":"variation","start":140560820,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1415769765","clinical_significance":[]},{"seq_region_name":"7","id":"rs962287987","clinical_significance":[],"strand":1,"feature_type":"variation","end":140560825,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560825,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs547244819","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560826,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140560826},{"alleles":["G","A","C"],"end":140560827,"strand":1,"feature_type":"variation","start":140560827,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs918621354","clinical_significance":[]},{"clinical_significance":[],"id":"rs955341814","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560832,"feature_type":"variation","strand":1,"end":140560832,"alleles":["G","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1301974150","source":"dbSNP","start":140560833,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140560833,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1233939871","seq_region_name":"7","source":"dbSNP","start":140560837,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140560837,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1422666014","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560841,"source":"dbSNP","strand":1,"feature_type":"variation","end":140560841,"alleles":["T","G"]},{"start":140560842,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140560842,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1295788035","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140560844,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560844,"source":"dbSNP","seq_region_name":"7","id":"rs1797583155","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140560855,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560855,"source":"dbSNP","id":"rs1585634368","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs889528509","feature_type":"variation","strand":1,"end":140560856,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560856},{"strand":1,"feature_type":"variation","end":140560858,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560858,"source":"dbSNP","seq_region_name":"7","id":"rs1382386023","clinical_significance":[]},{"alleles":["G","T"],"end":140560860,"feature_type":"variation","strand":1,"source":"dbSNP","start":140560860,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1297024491"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1006554000","source":"dbSNP","start":140560861,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140560861,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs986920944","clinical_significance":[],"end":140560864,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140560864,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1585634438","seq_region_name":"7","clinical_significance":[],"start":140560873,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140560873,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1797584048","clinical_significance":[],"strand":1,"feature_type":"variation","end":140560875,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560875,"source":"dbSNP"},{"seq_region_name":"7","id":"rs911300543","clinical_significance":[],"start":140560882,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140560882,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560883,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140560883,"id":"rs1370613929","seq_region_name":"7","clinical_significance":[]},{"id":"rs1797584353","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560885,"source":"dbSNP","strand":1,"feature_type":"variation","end":140560885,"alleles":["G","A"]},{"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140560886,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560886,"clinical_significance":[],"id":"rs1797584457","seq_region_name":"7"},{"id":"rs2130574750","seq_region_name":"7","clinical_significance":[],"end":140560887,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140560887,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1477543635","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560888,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140560888},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797584650","feature_type":"variation","strand":1,"end":140560889,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560889},{"seq_region_name":"7","id":"rs1797584741","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140560890,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560890,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1411153766","clinical_significance":[],"alleles":["A","G"],"end":140560891,"strand":1,"feature_type":"variation","start":140560891,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs957170252","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560892,"feature_type":"variation","strand":1,"end":140560892,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs942762758","clinical_significance":[],"end":140560897,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140560897,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560900,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140560900,"clinical_significance":[],"seq_region_name":"7","id":"rs2130574804"},{"seq_region_name":"7","id":"rs1797585172","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560910,"source":"dbSNP","strand":1,"feature_type":"variation","end":140560910,"alleles":["G","A"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560912,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140560912,"seq_region_name":"7","id":"rs571855597","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs971457638","source":"dbSNP","start":140560913,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140560913,"alleles":["G","A"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140560917,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560917,"clinical_significance":[],"id":"rs1797585539","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140560920,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560920,"source":"dbSNP","seq_region_name":"7","id":"rs1797585640","clinical_significance":[]},{"seq_region_name":"7","id":"rs925449830","clinical_significance":[],"start":140560922,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140560922,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs74570683","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560925,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140560925},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560925,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CGCT","-"],"end":140560928,"seq_region_name":"7","id":"rs1441858675","clinical_significance":[]},{"seq_region_name":"7","id":"rs73491570","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560926,"source":"dbSNP","strand":1,"feature_type":"variation","end":140560926,"alleles":["G","A","T"]},{"seq_region_name":"7","id":"rs1244375191","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140560927,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560927,"source":"dbSNP"},{"alleles":["AA","AAAAAA"],"end":140560930,"feature_type":"variation","strand":1,"source":"dbSNP","start":140560929,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1554468445"},{"clinical_significance":[],"id":"rs896179067","seq_region_name":"7","feature_type":"variation","strand":1,"end":140560931,"alleles":["G","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560931},{"alleles":["A","G"],"end":140560932,"feature_type":"variation","strand":1,"source":"dbSNP","start":140560932,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1324316502"},{"start":140560932,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AAAAAAAAAA","AAAAAAAAA","AAAAAAAAAAA","AAAAAAAAAAAAAAAAAA"],"end":140560941,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs201719342","clinical_significance":[]},{"start":140560933,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140560933,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797586937","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140560937,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560937,"source":"dbSNP","seq_region_name":"7","id":"rs1013197543","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1277184641","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560939,"feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140560939},{"clinical_significance":[],"seq_region_name":"7","id":"rs1414802308","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560941,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140560941},{"seq_region_name":"7","id":"rs1044678543","clinical_significance":[],"alleles":["A","G"],"end":140560944,"strand":1,"feature_type":"variation","start":140560944,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1356835786","alleles":["G","A","T"],"end":140560948,"feature_type":"variation","strand":1,"source":"dbSNP","start":140560948,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140560951,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140560951,"alleles":["G","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797588386","clinical_significance":[]},{"seq_region_name":"7","id":"rs1342898224","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140560952,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560952,"source":"dbSNP"},{"alleles":["A","G"],"end":140560953,"strand":1,"feature_type":"variation","start":140560953,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797588607","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797588738","end":140560958,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140560958,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140560960,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140560960,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797588835","clinical_significance":[]},{"start":140560962,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140560962,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs771833005","clinical_significance":[]},{"start":140560963,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140560963,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1397190492","clinical_significance":[]},{"clinical_significance":[],"id":"rs1797589387","seq_region_name":"7","end":140560964,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140560964,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140560966,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140560966,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797589553"},{"strand":1,"feature_type":"variation","end":140560972,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560972,"source":"dbSNP","seq_region_name":"7","id":"rs1005946632","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140560974,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560974,"source":"dbSNP","seq_region_name":"7","id":"rs1169419152","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797590019","clinical_significance":[],"start":140560979,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140560979,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560981,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140560981,"clinical_significance":[],"id":"rs2130575089","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140560985,"alleles":["AAA","AA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560983,"clinical_significance":[],"seq_region_name":"7","id":"rs1460339170"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140560988,"source":"dbSNP","strand":1,"feature_type":"variation","end":140560988,"alleles":["C","G","T"],"id":"rs766690","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560988,"feature_type":"variation","strand":1,"alleles":["CG","-"],"end":140560989,"clinical_significance":[],"seq_region_name":"7","id":"rs1423105320"},{"clinical_significance":[],"id":"rs961892984","seq_region_name":"7","source":"dbSNP","start":140560989,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140560989,"alleles":["G","A","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797591156","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560991,"feature_type":"variation","strand":1,"end":140560991,"alleles":["G","A"]},{"clinical_significance":[],"id":"rs1186985449","seq_region_name":"7","feature_type":"variation","strand":1,"end":140560992,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140560992},{"feature_type":"variation","strand":1,"end":140561006,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561006,"clinical_significance":[],"seq_region_name":"7","id":"rs1438884755"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561011,"feature_type":"variation","strand":1,"alleles":["C","-"],"end":140561011,"clinical_significance":[],"seq_region_name":"7","id":"rs1437451223"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1036644163","alleles":["A","C"],"end":140561016,"feature_type":"variation","strand":1,"source":"dbSNP","start":140561016,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs993438985","clinical_significance":[],"alleles":["T","A","C","G"],"end":140561017,"strand":1,"feature_type":"variation","start":140561017,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1238957158","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561022,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C","T"],"end":140561022},{"seq_region_name":"7","id":"rs1030252620","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140561024,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561024,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140561031,"alleles":["TTTTTTTT","TTTTTTT","TTTTTTTTT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561024,"clinical_significance":[],"id":"rs923509588","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140561026,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561026,"source":"dbSNP","seq_region_name":"7","id":"rs955390896","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140561027,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561027,"source":"dbSNP","seq_region_name":"7","id":"rs1797593676","clinical_significance":[]},{"id":"rs1797593824","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561029,"source":"dbSNP","strand":1,"feature_type":"variation","end":140561037,"alleles":["TTTCTTTCT","TTTCT"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561032,"feature_type":"variation","strand":1,"end":140561032,"alleles":["C","T"],"clinical_significance":[],"id":"rs1182864625","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561033,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140561033,"clinical_significance":[],"seq_region_name":"7","id":"rs1330822805"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561036,"source":"dbSNP","strand":1,"feature_type":"variation","end":140561036,"alleles":["C","T"],"seq_region_name":"7","id":"rs1390747515","clinical_significance":[]},{"end":140561038,"alleles":["A","G","T"],"strand":1,"feature_type":"variation","start":140561038,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs986805154","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561043,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140561043,"seq_region_name":"7","id":"rs1585634914","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140561044,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561044,"clinical_significance":[],"seq_region_name":"7","id":"rs2130575302"},{"clinical_significance":[],"id":"rs911183991","seq_region_name":"7","feature_type":"variation","strand":1,"end":140561046,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561046},{"seq_region_name":"7","id":"rs1797595121","clinical_significance":[],"strand":1,"feature_type":"variation","end":140561047,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561047,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140561049,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561049,"clinical_significance":[],"id":"rs1797595304","seq_region_name":"7"},{"end":140561050,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140561050,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797595464","clinical_significance":[]},{"id":"rs1797595635","seq_region_name":"7","clinical_significance":[],"start":140561054,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["-","A"],"end":140561053,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140561054,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140561054,"alleles":["T","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs964492692"},{"seq_region_name":"7","id":"rs1797596004","clinical_significance":[],"strand":1,"feature_type":"variation","end":140561063,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561063,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561065,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140561065,"clinical_significance":[],"seq_region_name":"7","id":"rs1797596127"},{"source":"dbSNP","start":140561068,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140561068,"alleles":["G","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797596213"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561070,"feature_type":"variation","strand":1,"end":140561070,"alleles":["C","A"],"clinical_significance":[],"id":"rs1585634947","seq_region_name":"7"},{"source":"dbSNP","start":140561086,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140561086,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1395213548"},{"strand":1,"feature_type":"variation","end":140561091,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561091,"source":"dbSNP","id":"rs1797596570","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130575402","alleles":["-","GTGCAGTGGTGTGAT"],"end":140561092,"feature_type":"variation","strand":1,"source":"dbSNP","start":140561093,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130575418","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561097,"feature_type":"variation","strand":1,"end":140561096,"alleles":["-","GCTC"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1165877358","source":"dbSNP","start":140561097,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G","T"],"end":140561097,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs2130575443","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["-","CTGC"],"end":140561097,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561098,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130575455","source":"dbSNP","start":140561100,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140561099,"alleles":["-","GGGTTCTCTGCG"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs74825156","alleles":["C","G"],"end":140561101,"feature_type":"variation","strand":1,"source":"dbSNP","start":140561101,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140561102,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140561102,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1563142079","clinical_significance":[]},{"end":140561104,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140561104,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs925472099","seq_region_name":"7","clinical_significance":[]},{"start":140561106,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140561106,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1416031111","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140561107,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561107,"clinical_significance":[],"seq_region_name":"7","id":"rs935482447"},{"clinical_significance":[],"id":"rs1797597621","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140561117,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561117},{"start":140561118,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C","G"],"end":140561118,"strand":1,"feature_type":"variation","id":"rs554934329","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561134,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C","T"],"end":140561134,"seq_region_name":"7","id":"rs918176959","clinical_significance":[]},{"end":140561138,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140561138,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1235045797","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140561141,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561141,"source":"dbSNP","id":"rs1797598321","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797598426","source":"dbSNP","start":140561142,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140561142,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1385404569","source":"dbSNP","start":140561147,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140561147,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140561148,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561148,"clinical_significance":[],"seq_region_name":"7","id":"rs2030563"},{"strand":1,"feature_type":"variation","end":140561153,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561153,"source":"dbSNP","seq_region_name":"7","id":"rs1054117413","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561155,"feature_type":"variation","strand":1,"end":140561155,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1797599025"},{"source":"dbSNP","start":140561156,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140561156,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585635083"},{"start":140561161,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140561161,"alleles":["C","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797599250","clinical_significance":[]},{"clinical_significance":[],"id":"rs2130575609","seq_region_name":"7","feature_type":"variation","strand":1,"end":140561162,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561162},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140561164,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561164,"clinical_significance":[],"seq_region_name":"7","id":"rs1585635089"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140561167,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561167,"clinical_significance":[],"seq_region_name":"7","id":"rs1797599433"},{"source":"dbSNP","start":140561179,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140561179,"alleles":["T","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1044729506"},{"feature_type":"variation","strand":1,"end":140561184,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561184,"clinical_significance":[],"seq_region_name":"7","id":"rs1797599676"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561184,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TTTT","TTT"],"end":140561187,"seq_region_name":"7","id":"rs1287381021","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130575645","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561189,"source":"dbSNP","strand":1,"feature_type":"variation","end":140561189,"alleles":["A","G"]},{"alleles":["G","A"],"end":140561190,"strand":1,"feature_type":"variation","start":140561190,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs2130575649","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1227186200","end":140561193,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140561193,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1281163767","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561195,"source":"dbSNP","strand":1,"feature_type":"variation","end":140561195,"alleles":["A","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1237911501","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561199,"feature_type":"variation","strand":1,"end":140561199,"alleles":["C","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561203,"source":"dbSNP","strand":1,"feature_type":"variation","end":140561203,"alleles":["T","C"],"seq_region_name":"7","id":"rs904829333","clinical_significance":[]},{"source":"dbSNP","start":140561210,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140561210,"alleles":["T","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1326309679"},{"start":140561215,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140561215,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797600438","clinical_significance":[]},{"clinical_significance":[],"id":"rs1442914633","seq_region_name":"7","source":"dbSNP","start":140561216,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140561216,"feature_type":"variation","strand":1},{"alleles":["G","T"],"end":140561225,"strand":1,"feature_type":"variation","start":140561225,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1797600658","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561237,"source":"dbSNP","strand":1,"feature_type":"variation","end":140561237,"alleles":["A","T"],"seq_region_name":"7","id":"rs1797600764","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs534581649","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561241,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140561241},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561244,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140561244,"seq_region_name":"7","id":"rs1392468933","clinical_significance":[]},{"seq_region_name":"7","id":"rs1323156014","clinical_significance":[],"strand":1,"feature_type":"variation","end":140561245,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561245,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs185431310","source":"dbSNP","start":140561246,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140561246,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797601327","end":140561259,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140561259,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140561266,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561266,"clinical_significance":[],"id":"rs1486220918","seq_region_name":"7"},{"end":140561267,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140561267,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1797601522","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1410293616","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561271,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140561271},{"alleles":["C","T"],"end":140561274,"strand":1,"feature_type":"variation","start":140561274,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1156935037","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1229626659","feature_type":"variation","strand":1,"end":140561277,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561277},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561278,"feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140561278,"clinical_significance":[],"seq_region_name":"7","id":"rs1585635294"},{"clinical_significance":[],"id":"rs1249686911","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561280,"feature_type":"variation","strand":1,"end":140561280,"alleles":["C","A"]},{"source":"dbSNP","start":140561288,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140561288,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1338870545"},{"end":140561298,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","start":140561298,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1020241923","clinical_significance":[]},{"clinical_significance":[],"id":"rs1797602439","seq_region_name":"7","source":"dbSNP","start":140561299,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140561299,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797602536","alleles":["G","A"],"end":140561301,"feature_type":"variation","strand":1,"source":"dbSNP","start":140561301,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1037439369","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561304,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140561304},{"seq_region_name":"7","id":"rs897694507","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561307,"source":"dbSNP","strand":1,"feature_type":"variation","end":140561307,"alleles":["T","C"]},{"strand":1,"feature_type":"variation","end":140561310,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561310,"source":"dbSNP","seq_region_name":"7","id":"rs1797602882","clinical_significance":[]},{"clinical_significance":[],"id":"rs1467423334","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561315,"feature_type":"variation","strand":1,"end":140561324,"alleles":["TGTTGTTGTT","TGTTGTT"]},{"id":"rs558177069","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140561319,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561319,"source":"dbSNP"},{"source":"dbSNP","start":140561329,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140561329,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1220406791"},{"start":140561330,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140561330,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs545192670","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797603443","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561334,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140561334},{"seq_region_name":"7","id":"rs2130575891","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140561338,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561338,"source":"dbSNP"},{"alleles":["G","A"],"end":140561340,"strand":1,"feature_type":"variation","start":140561340,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs993321125","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797603566","feature_type":"variation","strand":1,"end":140561349,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561349},{"source":"dbSNP","start":140561351,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140561351,"alleles":["T","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797603669"},{"source":"dbSNP","start":140561355,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140561355,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1202807752"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1459785034","feature_type":"variation","strand":1,"alleles":["T","-"],"end":140561355,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561355},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797604012","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140561357,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561357},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561366,"feature_type":"variation","strand":1,"end":140561366,"alleles":["A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1797604132"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1352891806","feature_type":"variation","strand":1,"end":140561367,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561367},{"feature_type":"variation","strand":1,"end":140561371,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561371,"clinical_significance":[],"seq_region_name":"7","id":"rs1030133328"},{"alleles":["T","A"],"end":140561377,"feature_type":"variation","strand":1,"source":"dbSNP","start":140561377,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130575977"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797605385","feature_type":"variation","strand":1,"end":140561380,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561380},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797605475","source":"dbSNP","start":140561383,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140561383,"alleles":["T","C"],"feature_type":"variation","strand":1},{"end":140561387,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140561387,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs143290319","clinical_significance":[]},{"start":140561390,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140561390,"alleles":["A","G"],"strand":1,"feature_type":"variation","id":"rs2130575998","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797605705","clinical_significance":[],"start":140561391,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140561391,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140561400,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140561400,"alleles":["A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797605814"},{"id":"rs147544684","seq_region_name":"7","clinical_significance":[],"start":140561412,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140561412,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140561415,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561415,"source":"dbSNP","id":"rs543082600","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1431710823","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561423,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140561423},{"end":140561426,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140561426,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs561262760","clinical_significance":[]},{"seq_region_name":"7","id":"rs1191017567","clinical_significance":[],"alleles":["T","C"],"end":140561427,"strand":1,"feature_type":"variation","start":140561427,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797606530","source":"dbSNP","start":140561429,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140561429,"feature_type":"variation","strand":1},{"end":140561430,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140561430,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1347223276"},{"alleles":["G","T"],"end":140561431,"feature_type":"variation","strand":1,"source":"dbSNP","start":140561431,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs75644999"},{"end":140561432,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140561432,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs964064095","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797607085","clinical_significance":[],"strand":1,"feature_type":"variation","end":140561442,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561442,"source":"dbSNP"},{"seq_region_name":"7","id":"rs979948351","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561446,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140561446},{"feature_type":"variation","strand":1,"end":140561447,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561447,"clinical_significance":[],"seq_region_name":"7","id":"rs776230361"},{"start":140561448,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140561448,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs540896260","clinical_significance":[]},{"end":140561450,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140561450,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs189942845","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1424945286","end":140561453,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140561453,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561457,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["-","T","TATTTATAACGTCTAACC"],"end":140561456,"id":"rs1797607865","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797607991","alleles":["A","T"],"end":140561457,"feature_type":"variation","strand":1,"source":"dbSNP","start":140561457,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140561458,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140561457,"alleles":["-","TTTATAACGTCTAACCT"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797608097"},{"source":"dbSNP","start":140561458,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140561458,"alleles":["A","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1797608203","seq_region_name":"7"},{"start":140561464,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140561464,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs182522674","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs988271183","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561465,"feature_type":"variation","strand":1,"end":140561465,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs918063742","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140561467,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561467},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561468,"feature_type":"variation","strand":1,"end":140561468,"alleles":["T","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1797608655"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561472,"source":"dbSNP","strand":1,"feature_type":"variation","end":140561472,"alleles":["C","A"],"id":"rs1797608756","seq_region_name":"7","clinical_significance":[]},{"id":"rs1797608868","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140561473,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561473,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561474,"source":"dbSNP","strand":1,"feature_type":"variation","end":140561474,"alleles":["A","G"],"seq_region_name":"7","id":"rs1797608982","clinical_significance":[]},{"end":140561475,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140561475,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs949651840","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1487682839","source":"dbSNP","start":140561476,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140561476,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140561477,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140561482,"alleles":["TTTTTT","TTTTTTT"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1190790738"},{"alleles":["TTTCTTTCTTTCT","TTTCTTTCT"],"end":140561492,"feature_type":"variation","strand":1,"source":"dbSNP","start":140561480,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1280894417"},{"feature_type":"variation","strand":1,"end":140561482,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561482,"clinical_significance":[],"seq_region_name":"7","id":"rs1797609549"},{"end":140561483,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140561483,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585635644"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585635654","end":140561487,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140561487,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140561495,"alleles":["TTCTGTT","TT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140561489,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1212974682"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797609984","source":"dbSNP","start":140561491,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140561491,"feature_type":"variation","strand":1},{"start":140561491,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140561491,"alleles":["C","-"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130576263","clinical_significance":[]},{"clinical_significance":[],"id":"rs981035579","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561493,"feature_type":"variation","strand":1,"end":140561493,"alleles":["G","A","T"]},{"feature_type":"variation","strand":1,"alleles":["G","-"],"end":140561493,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561493,"clinical_significance":[],"id":"rs1797610199","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1585635681","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561496,"source":"dbSNP","strand":1,"feature_type":"variation","end":140561496,"alleles":["G","T"]},{"end":140561496,"alleles":["G","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140561496,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797610411"},{"start":140561497,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140561497,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797610505","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1277623915","end":140561499,"alleles":["TCT","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140561497,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140561500,"alleles":["TCTT","TCTTCTT"],"strand":1,"feature_type":"variation","start":140561497,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797610718","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797610817","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["TCTTTTTTTTTTTTTTTTTTTTT","TCTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTT"],"end":140561519,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561497,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1222288252","seq_region_name":"7","feature_type":"variation","strand":1,"end":140561498,"alleles":["C","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561498},{"clinical_significance":[],"seq_region_name":"7","id":"rs1276550013","source":"dbSNP","start":140561498,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140561498,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140561499,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140561499,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1389924718","seq_region_name":"7"},{"alleles":["T","TGTTTTTT"],"end":140561499,"strand":1,"feature_type":"variation","start":140561499,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs2130576353","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140561519,"alleles":["TTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTT","TTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561499,"clinical_significance":[],"seq_region_name":"7","id":"rs536896244"},{"clinical_significance":[],"id":"rs1797612170","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561500,"feature_type":"variation","strand":1,"end":140561500,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1797612284","clinical_significance":[],"end":140561504,"alleles":["-","C"],"strand":1,"feature_type":"variation","start":140561505,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1171550110","source":"dbSNP","start":140561505,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140561505,"alleles":["T","A"],"feature_type":"variation","strand":1},{"alleles":["T","G"],"end":140561507,"feature_type":"variation","strand":1,"source":"dbSNP","start":140561507,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1415808034"},{"seq_region_name":"7","id":"rs2130576481","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140561513,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561513,"source":"dbSNP"},{"alleles":["T","C"],"end":140561516,"feature_type":"variation","strand":1,"source":"dbSNP","start":140561516,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1384390698"},{"feature_type":"variation","strand":1,"end":140561520,"alleles":["TTTG","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561517,"clinical_significance":[],"seq_region_name":"7","id":"rs1797612671"},{"start":140561518,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140561518,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1191091429","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1294121090","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561518,"feature_type":"variation","strand":1,"end":140561520,"alleles":["TTG","-"]},{"end":140561520,"alleles":["TG","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140561519,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1325881456"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1234098683","source":"dbSNP","start":140561520,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","-"],"end":140561520,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140561520,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561520,"source":"dbSNP","seq_region_name":"7","id":"rs1285363652","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140561523,"alleles":["GAGA","GA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561520,"clinical_significance":[],"seq_region_name":"7","id":"rs1797613333"},{"id":"rs1321692186","seq_region_name":"7","clinical_significance":[],"end":140561521,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140561521,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140561522,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140561522,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130576563","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1203343574","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561523,"feature_type":"variation","strand":1,"end":140561523,"alleles":["A","G","T"]},{"seq_region_name":"7","id":"rs2130576582","clinical_significance":[],"end":140561524,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140561524,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140561528,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561528,"source":"dbSNP","seq_region_name":"7","id":"rs2130576589","clinical_significance":[]},{"clinical_significance":[],"id":"rs1585635845","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140561531,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561531},{"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140561532,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561532,"clinical_significance":[],"seq_region_name":"7","id":"rs1236899556"},{"source":"dbSNP","start":140561534,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C","G","T"],"end":140561534,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs10808051","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140561543,"alleles":["ATGTCGCCCA","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561534,"clinical_significance":[],"seq_region_name":"7","id":"rs1023878049"},{"source":"dbSNP","start":140561538,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140561538,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1203285606","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561539,"feature_type":"variation","strand":1,"end":140561539,"alleles":["G","A","T"],"clinical_significance":[],"id":"rs1260980081","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140561540,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561540,"clinical_significance":[],"seq_region_name":"7","id":"rs1797614461"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561546,"feature_type":"variation","strand":1,"end":140561546,"alleles":["C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1451635879"},{"id":"rs1742723168","seq_region_name":"7","clinical_significance":[],"end":140561548,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140561548,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs796412787","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561549,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140561549},{"source":"dbSNP","start":140561550,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140561550,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585635942"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561552,"source":"dbSNP","strand":1,"feature_type":"variation","end":140561552,"alleles":["T","G"],"seq_region_name":"7","id":"rs1050667662","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561554,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140561554,"seq_region_name":"7","id":"rs1585635971","clinical_significance":[]},{"alleles":["G","A"],"end":140561559,"feature_type":"variation","strand":1,"source":"dbSNP","start":140561559,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797615150"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130576716","feature_type":"variation","strand":1,"end":140561560,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561560},{"seq_region_name":"7","id":"rs1797615272","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140561577,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561577,"source":"dbSNP"},{"source":"dbSNP","start":140561579,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140561579,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1797615411","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1585635981","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140561586,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561586},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140561588,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561588,"source":"dbSNP","seq_region_name":"7","id":"rs1585635992","clinical_significance":[]},{"seq_region_name":"7","id":"rs910903664","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561590,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140561590},{"seq_region_name":"7","id":"rs1797615855","clinical_significance":[],"strand":1,"feature_type":"variation","end":140561591,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561591,"source":"dbSNP"},{"source":"dbSNP","start":140561592,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140561592,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs569773677","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140561595,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561595,"source":"dbSNP","seq_region_name":"7","id":"rs1797616094","clinical_significance":[]},{"seq_region_name":"7","id":"rs530519543","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561596,"source":"dbSNP","strand":1,"feature_type":"variation","end":140561596,"alleles":["T","C","G"]},{"seq_region_name":"7","id":"rs1797616342","clinical_significance":[],"strand":1,"feature_type":"variation","end":140561603,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561603,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1170463138","alleles":["A","T"],"end":140561608,"feature_type":"variation","strand":1,"source":"dbSNP","start":140561608,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140561609,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TTCT","T"],"end":140561612,"strand":1,"feature_type":"variation","id":"rs1797616565","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797616690","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561609,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TTCTCCT","T"],"end":140561615},{"seq_region_name":"7","id":"rs1464755731","clinical_significance":[],"end":140561611,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140561611,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1479897710","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561615,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140561615},{"seq_region_name":"7","id":"rs1159498842","clinical_significance":[],"alleles":["C","T"],"end":140561618,"strand":1,"feature_type":"variation","start":140561618,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["C","T"],"end":140561626,"feature_type":"variation","strand":1,"source":"dbSNP","start":140561626,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585636050"},{"start":140561628,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140561628,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1413136023","clinical_significance":[]},{"clinical_significance":[],"id":"rs534422575","seq_region_name":"7","end":140561629,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140561629,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140561632,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140561632,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs371215980"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1412909989","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140561634,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561634},{"clinical_significance":[],"id":"rs1563142338","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561638,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140561638},{"strand":1,"feature_type":"variation","alleles":["G","C","T"],"end":140561639,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561639,"source":"dbSNP","seq_region_name":"7","id":"rs1054169725","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130576910","clinical_significance":[],"alleles":["A","T"],"end":140561640,"strand":1,"feature_type":"variation","start":140561640,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140561642,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561642,"source":"dbSNP","seq_region_name":"7","id":"rs892886335","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797618129","clinical_significance":[],"alleles":["C","T"],"end":140561644,"strand":1,"feature_type":"variation","start":140561644,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561650,"feature_type":"variation","strand":1,"end":140561650,"alleles":["T","A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs146269255"},{"clinical_significance":[],"id":"rs1797618418","seq_region_name":"7","feature_type":"variation","strand":1,"end":140561652,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561652},{"seq_region_name":"7","id":"rs2130576959","clinical_significance":[],"alleles":["A","C"],"end":140561653,"strand":1,"feature_type":"variation","start":140561653,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["A","C"],"end":140561656,"strand":1,"feature_type":"variation","start":140561656,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585636143","clinical_significance":[]},{"end":140561658,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140561658,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797618609"},{"seq_region_name":"7","id":"rs1585636150","clinical_significance":[],"start":140561659,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140561659,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1034826558","clinical_significance":[],"start":140561661,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C","T"],"end":140561661,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561662,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140561662,"seq_region_name":"7","id":"rs1343794667","clinical_significance":[]},{"start":140561663,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140561663,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1236106827","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797619210","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140561664,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561664,"source":"dbSNP"},{"start":140561665,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C","T"],"end":140561665,"strand":1,"feature_type":"variation","id":"rs1585636196","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1223098730","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561666,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C","T"],"end":140561666},{"end":140561667,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140561667,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1585636237","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797619740","feature_type":"variation","strand":1,"alleles":["T","TT"],"end":140561668,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561668},{"seq_region_name":"7","id":"rs1225942808","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561669,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140561669},{"strand":1,"feature_type":"variation","end":140561669,"alleles":["A","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561669,"source":"dbSNP","id":"rs1289270387","seq_region_name":"7","clinical_significance":[]},{"end":140561670,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140561670,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1797620063","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140561686,"alleles":["TTTTTTTTTTTTTTTTT","TTTTTTTTT","TTTTTTTTTT","TTTTTTTTTTTT","TTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561670,"clinical_significance":[],"seq_region_name":"7","id":"rs1242616480"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1394676395","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561677,"feature_type":"variation","strand":1,"end":140561677,"alleles":["T","G"]},{"end":140561688,"alleles":["TTTTTTTTTTGT","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140561677,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs756981608"},{"start":140561677,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TTTTTTTTTTGTATTTT","TTTT"],"end":140561693,"strand":1,"feature_type":"variation","id":"rs753668060","seq_region_name":"7","clinical_significance":[]},{"end":140561678,"alleles":["T","A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140561678,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585636339"},{"end":140561688,"alleles":["TTTTTTTTTGT","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140561678,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1554468666"},{"source":"dbSNP","start":140561678,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140561693,"alleles":["TTTTTTTTTGTATTTT","TTTT"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs71173211"},{"source":"dbSNP","start":140561679,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140561679,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1348829548"},{"source":"dbSNP","start":140561679,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TTTTTTTTGTATTTT","TTTT"],"end":140561693,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1260006641"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1159252191","alleles":["-","A"],"end":140561679,"feature_type":"variation","strand":1,"source":"dbSNP","start":140561680,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["T","A"],"end":140561680,"feature_type":"variation","strand":1,"source":"dbSNP","start":140561680,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797621885"},{"end":140561693,"alleles":["TTTTTTTGTATTTT","TTTT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140561680,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1356979413"},{"source":"dbSNP","start":140561681,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140561693,"alleles":["TTTTTTGTATTTT","TTTT"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1378468814"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561682,"source":"dbSNP","strand":1,"feature_type":"variation","end":140561682,"alleles":["T","C"],"seq_region_name":"7","id":"rs1585636399","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797622376","feature_type":"variation","strand":1,"end":140561688,"alleles":["TTTTTGT","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561682},{"clinical_significance":[],"seq_region_name":"7","id":"rs1177771739","feature_type":"variation","strand":1,"alleles":["TTTTTGTATTTT","TTTT"],"end":140561693,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561682},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561682,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TTTTTGTATTTTCAGTAGAGA","-"],"end":140561702,"seq_region_name":"7","id":"rs1454554627","clinical_significance":[]},{"clinical_significance":[],"id":"rs1266114157","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561683,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140561683},{"end":140561693,"alleles":["TTTTGTATTTT","TTTT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140561683,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1224701872"},{"seq_region_name":"7","id":"rs1797622962","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561683,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TTTTGTATTTTC","-"],"end":140561694},{"clinical_significance":[],"id":"rs1797623070","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["TTTGTATTTTC","-"],"end":140561694,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561684},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797623182","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561685,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140561685},{"seq_region_name":"7","id":"rs1797623290","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561686,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TGT","T"],"end":140561688},{"seq_region_name":"7","id":"rs2130577311","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561687,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["-","TTTTTTTCTTCCTCAGCCTCCCG"],"end":140561686},{"clinical_significance":[],"seq_region_name":"7","id":"rs12531421","source":"dbSNP","start":140561687,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140561687,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs370115011","feature_type":"variation","strand":1,"alleles":["G","-"],"end":140561687,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561687},{"end":140561689,"alleles":["GTA","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140561687,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1261361980"},{"start":140561687,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140561699,"alleles":["GTATTTTCAGTAG","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1563142416","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs10464457","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561688,"feature_type":"variation","strand":1,"alleles":["T","A","G"],"end":140561688},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130577365","end":140561688,"alleles":["-","GTGGTGGG"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140561689,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140561689,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C","T"],"end":140561689,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs12534455","clinical_significance":[]},{"clinical_significance":[],"id":"rs1352139552","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","AA"],"end":140561689,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561689},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563142430","end":140561689,"alleles":["A","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140561689,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs2130577398","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561690,"feature_type":"variation","strand":1,"alleles":["TTTT","TTTTTGGGGTTCTCCTCCACTCCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT"],"end":140561693},{"source":"dbSNP","start":140561694,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140561694,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1252269836"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1554468695","source":"dbSNP","start":140561694,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140561707,"alleles":["CAGTAGAGACAGGG","-"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561695,"feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140561695,"clinical_significance":[],"seq_region_name":"7","id":"rs1421187740"},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140561696,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561696,"source":"dbSNP","id":"rs1554468697","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs746415112","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561697,"feature_type":"variation","strand":1,"alleles":["TAGAGACAGGGTT","T"],"end":140561709},{"strand":1,"feature_type":"variation","end":140561698,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561698,"source":"dbSNP","id":"rs1797625012","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561700,"feature_type":"variation","strand":1,"end":140561700,"alleles":["A","G"],"clinical_significance":[],"id":"rs1797625112","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561701,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140561701,"clinical_significance":[],"seq_region_name":"7","id":"rs534619194"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561704,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140561704,"clinical_significance":[],"seq_region_name":"7","id":"rs1797625346"},{"seq_region_name":"7","id":"rs1797625442","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561705,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140561705},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563142460","source":"dbSNP","start":140561706,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["GGT","-"],"end":140561708,"feature_type":"variation","strand":1},{"id":"rs1458865469","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140561707,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561707,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1302907096","source":"dbSNP","start":140561711,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140561711,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561714,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140561714,"clinical_significance":[],"seq_region_name":"7","id":"rs1797625874"},{"start":140561716,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140561716,"alleles":["T","A","C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs4726898","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140561717,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561717,"clinical_significance":[],"id":"rs571354066","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140561720,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561720,"clinical_significance":[],"seq_region_name":"7","id":"rs1797626394"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1037891649","source":"dbSNP","start":140561721,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140561721,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs897579477","end":140561727,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140561727,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1421065402","source":"dbSNP","start":140561728,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140561728,"alleles":["T","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1358477184","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561729,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140561729},{"seq_region_name":"7","id":"rs1797626965","clinical_significance":[],"start":140561731,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140561731,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs928998101","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561732,"feature_type":"variation","strand":1,"end":140561732,"alleles":["C","T"]},{"feature_type":"variation","strand":1,"alleles":["CTCCTGGCCTC","CTC"],"end":140561748,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561738,"clinical_significance":[],"seq_region_name":"7","id":"rs1435057650"},{"feature_type":"variation","strand":1,"end":140561739,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561739,"clinical_significance":[],"seq_region_name":"7","id":"rs1003221877"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561744,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140561744,"seq_region_name":"7","id":"rs1404432938","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1051614540","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561750,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140561750},{"strand":1,"feature_type":"variation","end":140561755,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561755,"source":"dbSNP","seq_region_name":"7","id":"rs1034249658","clinical_significance":[]},{"end":140561764,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140561764,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs890262368","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797627848","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140561767,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561767},{"clinical_significance":[],"seq_region_name":"7","id":"rs538783445","end":140561768,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140561768,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140561769,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140561770,"alleles":["CC","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1797628079","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140561770,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561770,"source":"dbSNP","seq_region_name":"7","id":"rs1797628276","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1262776164","source":"dbSNP","start":140561772,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140561772,"alleles":["C","T"],"feature_type":"variation","strand":1},{"id":"rs1006217567","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140561773,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561773,"source":"dbSNP"},{"seq_region_name":"7","id":"rs2130577686","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561778,"source":"dbSNP","strand":1,"feature_type":"variation","end":140561778,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs1487356116","clinical_significance":[],"start":140561780,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140561779,"alleles":["-","C"],"strand":1,"feature_type":"variation"},{"id":"rs1797630143","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561790,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140561790},{"start":140561795,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140561795,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797630262","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797630365","clinical_significance":[],"strand":1,"feature_type":"variation","end":140561798,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561798,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1285874133","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561801,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140561801},{"alleles":["A","C"],"end":140561802,"feature_type":"variation","strand":1,"source":"dbSNP","start":140561802,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797630573"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1017501629","alleles":["C","T"],"end":140561803,"feature_type":"variation","strand":1,"source":"dbSNP","start":140561803,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140561804,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140561804,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs556865875"},{"start":140561809,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140561809,"strand":1,"feature_type":"variation","id":"rs1300529578","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140561812,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561812,"clinical_significance":[],"seq_region_name":"7","id":"rs1788437796"},{"source":"dbSNP","start":140561815,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140561815,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1797631045","seq_region_name":"7"},{"id":"rs1797631145","seq_region_name":"7","clinical_significance":[],"end":140561816,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140561816,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797631263","source":"dbSNP","start":140561818,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140561818,"alleles":["A","T"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140561824,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140561824,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1389401577"},{"start":140561828,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140561828,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797631471","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140561832,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561832,"clinical_significance":[],"seq_region_name":"7","id":"rs899870069"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140561833,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561833,"source":"dbSNP","seq_region_name":"7","id":"rs575738091","clinical_significance":[]},{"alleles":["T","C"],"end":140561836,"feature_type":"variation","strand":1,"source":"dbSNP","start":140561836,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585636836"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1306005592","feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140561840,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561840},{"id":"rs1032718589","seq_region_name":"7","clinical_significance":[],"start":140561843,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140561843,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs750784225","clinical_significance":[],"start":140561844,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140561844,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1322174922","clinical_significance":[],"alleles":["C","G","T"],"end":140561846,"strand":1,"feature_type":"variation","start":140561846,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1297084155","clinical_significance":[],"strand":1,"feature_type":"variation","end":140561852,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561852,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1016396746","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561857,"source":"dbSNP","strand":1,"feature_type":"variation","end":140561857,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797632574","end":140561862,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140561862,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140561865,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561865,"clinical_significance":[],"seq_region_name":"7","id":"rs1404333702"},{"seq_region_name":"7","id":"rs569165434","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140561867,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561867,"source":"dbSNP"},{"end":140561879,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140561879,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs2130577880","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1585636921","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561883,"source":"dbSNP","strand":1,"feature_type":"variation","end":140561883,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs1373801051","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561884,"source":"dbSNP","strand":1,"feature_type":"variation","end":140561884,"alleles":["C","G"]},{"seq_region_name":"7","id":"rs972138389","clinical_significance":[],"alleles":["TTTATTTATTTATTTATT","TTTATTTATTTATT","TTTATTTATTTATTTATTTATT"],"end":140561902,"strand":1,"feature_type":"variation","start":140561885,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140561886,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140561886,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs954875207","clinical_significance":[]},{"seq_region_name":"7","id":"rs1358056516","clinical_significance":[],"end":140561887,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140561887,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs191814922","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561889,"feature_type":"variation","strand":1,"end":140561889,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs60480710","alleles":["T","G"],"end":140561891,"feature_type":"variation","strand":1,"source":"dbSNP","start":140561891,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs970852851","clinical_significance":[],"alleles":["T","C"],"end":140561904,"strand":1,"feature_type":"variation","start":140561904,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1479449116","seq_region_name":"7","source":"dbSNP","start":140561907,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140561907,"alleles":["T","C"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561910,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140561910,"clinical_significance":[],"id":"rs1254777425","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140561914,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561914,"source":"dbSNP","seq_region_name":"7","id":"rs1797634130","clinical_significance":[]},{"id":"rs1797634244","seq_region_name":"7","clinical_significance":[],"start":140561917,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140561917,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs942410532","alleles":["C","T"],"end":140561922,"feature_type":"variation","strand":1,"source":"dbSNP","start":140561922,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140561924,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140561924,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs981470881","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs914205194","source":"dbSNP","start":140561926,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140561926,"feature_type":"variation","strand":1},{"alleles":["T","C"],"end":140561927,"feature_type":"variation","strand":1,"source":"dbSNP","start":140561927,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797634673"},{"seq_region_name":"7","id":"rs1711850988","clinical_significance":[],"start":140561929,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140561929,"strand":1,"feature_type":"variation"},{"id":"rs926890023","seq_region_name":"7","clinical_significance":[],"start":140561931,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140561931,"alleles":["C","A","T"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140561932,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561932,"source":"dbSNP","seq_region_name":"7","id":"rs942240089","clinical_significance":[]},{"id":"rs1414937385","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561941,"source":"dbSNP","strand":1,"feature_type":"variation","end":140561941,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1342121817","end":140561943,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140561943,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561950,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140561950,"clinical_significance":[],"seq_region_name":"7","id":"rs2130578071"},{"seq_region_name":"7","id":"rs1332130526","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561952,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140561952},{"seq_region_name":"7","id":"rs766566494","clinical_significance":[],"start":140561954,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140561954,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs112249804","end":140561958,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140561958,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140561959,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140561959,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs929051982"},{"clinical_significance":[],"id":"rs1464245247","seq_region_name":"7","alleles":["G","T"],"end":140561960,"feature_type":"variation","strand":1,"source":"dbSNP","start":140561960,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797635825","source":"dbSNP","start":140561961,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140561961,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1423254447","seq_region_name":"7","end":140561964,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140561964,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs894393417","clinical_significance":[],"start":140561967,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140561967,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561968,"feature_type":"variation","strand":1,"end":140561968,"alleles":["C","A"],"clinical_significance":[],"id":"rs1797636152","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140561970,"feature_type":"variation","strand":1,"end":140561970,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585637220"},{"source":"dbSNP","start":140561973,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140561973,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1356410034"},{"source":"dbSNP","start":140561975,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140561975,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130578190"},{"source":"dbSNP","start":140561976,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140561976,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1585637239","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1473822246","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140561991,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140561991},{"id":"rs1797636708","seq_region_name":"7","clinical_significance":[],"end":140561993,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140561993,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1367178769","seq_region_name":"7","source":"dbSNP","start":140561994,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140561994,"alleles":["A","G"],"feature_type":"variation","strand":1},{"alleles":["T","G"],"end":140561998,"strand":1,"feature_type":"variation","start":140561998,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1051497224","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797637032","source":"dbSNP","start":140562002,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140562002,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562006,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140562006,"seq_region_name":"7","id":"rs1006101709","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585637289","end":140562010,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140562010,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562011,"feature_type":"variation","strand":1,"end":140562011,"alleles":["T","C"],"clinical_significance":[],"id":"rs1797637387","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1797637497","clinical_significance":[],"start":140562016,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140562016,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562018,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140562018,"clinical_significance":[],"id":"rs1297869887","seq_region_name":"7"},{"alleles":["T","A","C"],"end":140562027,"strand":1,"feature_type":"variation","start":140562027,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs911750642","clinical_significance":[]},{"end":140562028,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140562028,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1563142655"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562030,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140562030,"clinical_significance":[],"seq_region_name":"7","id":"rs1016278774"},{"end":140562036,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140562036,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1354279095","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","A"],"end":140562040,"feature_type":"variation","strand":1,"source":"dbSNP","start":140562040,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797638188"},{"alleles":["C","A","T"],"end":140562046,"strand":1,"feature_type":"variation","start":140562046,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs943214161","clinical_significance":[]},{"alleles":["G","A"],"end":140562047,"feature_type":"variation","strand":1,"source":"dbSNP","start":140562047,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs371693877"},{"feature_type":"variation","strand":1,"end":140562048,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562048,"clinical_significance":[],"seq_region_name":"7","id":"rs1797638570"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562049,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140562049,"seq_region_name":"7","id":"rs11764185","clinical_significance":[]},{"end":140562053,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140562053,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs2130578339","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562056,"feature_type":"variation","strand":1,"end":140562056,"alleles":["A","T"],"clinical_significance":[],"id":"rs1357873525","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562058,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140562058,"clinical_significance":[],"id":"rs1563142675","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140562061,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562061,"clinical_significance":[],"seq_region_name":"7","id":"rs539746742"},{"feature_type":"variation","strand":1,"alleles":["G","C","T"],"end":140562062,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562062,"clinical_significance":[],"seq_region_name":"7","id":"rs1797639184"},{"alleles":["A","G"],"end":140562064,"feature_type":"variation","strand":1,"source":"dbSNP","start":140562064,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1039395997"},{"end":140562077,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140562077,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs2130578382","seq_region_name":"7"},{"clinical_significance":[],"id":"rs558076814","seq_region_name":"7","end":140562078,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140562078,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs544839799","source":"dbSNP","start":140562079,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140562079,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140562083,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562083,"source":"dbSNP","id":"rs1585637444","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140562084,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562084,"clinical_significance":[],"seq_region_name":"7","id":"rs994004980"},{"seq_region_name":"7","id":"rs1797639916","clinical_significance":[],"start":140562089,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140562089,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1311166321","clinical_significance":[],"end":140562091,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140562091,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1797640122","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562092,"source":"dbSNP","strand":1,"feature_type":"variation","end":140562092,"alleles":["G","A","C"]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140562096,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562096,"source":"dbSNP","id":"rs1797640246","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140562105,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140562105,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797640356"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585637484","feature_type":"variation","strand":1,"end":140562107,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562107},{"clinical_significance":[],"seq_region_name":"7","id":"rs1297096750","feature_type":"variation","strand":1,"end":140562109,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562109},{"feature_type":"variation","strand":1,"end":140562110,"alleles":["G","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562110,"clinical_significance":[],"id":"rs1000497546","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562118,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140562118,"clinical_significance":[],"seq_region_name":"7","id":"rs1797640704"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797640810","end":140562120,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140562120,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140562121,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562121,"source":"dbSNP","seq_region_name":"7","id":"rs1053805438","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1388709661","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562123,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140562123},{"clinical_significance":[],"id":"rs1797641114","seq_region_name":"7","end":140562126,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140562126,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs868217901","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562127,"source":"dbSNP","strand":1,"feature_type":"variation","end":140562127,"alleles":["T","A"]},{"seq_region_name":"7","id":"rs892453662","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140562128,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562128,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797641438","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562132,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140562132},{"seq_region_name":"7","id":"rs1797641552","clinical_significance":[],"end":140562137,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140562137,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1470789669","source":"dbSNP","start":140562138,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140562138,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797641774","alleles":["T","C"],"end":140562139,"feature_type":"variation","strand":1,"source":"dbSNP","start":140562139,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1203345797","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562141,"source":"dbSNP","strand":1,"feature_type":"variation","end":140562141,"alleles":["G","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585637573","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140562146,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562146},{"end":140562148,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140562148,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1009632387","clinical_significance":[]},{"seq_region_name":"7","id":"rs1025013670","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140562149,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562149,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140562151,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562151,"clinical_significance":[],"seq_region_name":"7","id":"rs1256246402"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797642424","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562152,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140562152},{"seq_region_name":"7","id":"rs1585637601","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562154,"source":"dbSNP","strand":1,"feature_type":"variation","end":140562154,"alleles":["T","C"]},{"id":"rs1797642642","seq_region_name":"7","clinical_significance":[],"start":140562156,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140562156,"strand":1,"feature_type":"variation"},{"start":140562157,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140562157,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1177089407","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797642859","clinical_significance":[],"end":140562158,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140562158,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140562165,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140562165,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797642980","clinical_significance":[]},{"seq_region_name":"7","id":"rs1439485822","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562167,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140562167},{"clinical_significance":[],"id":"rs573374954","seq_region_name":"7","end":140562168,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140562168,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140562170,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562170,"clinical_significance":[],"seq_region_name":"7","id":"rs775822474"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1453014932","feature_type":"variation","strand":1,"end":140562174,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562174},{"alleles":["A","C"],"end":140562175,"feature_type":"variation","strand":1,"source":"dbSNP","start":140562175,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585637654"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562176,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140562176,"clinical_significance":[],"seq_region_name":"7","id":"rs1797643659"},{"strand":1,"feature_type":"variation","end":140562177,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562177,"source":"dbSNP","seq_region_name":"7","id":"rs1034222365","clinical_significance":[]},{"end":140562178,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140562178,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797643762","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs530551874","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562179,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140562179},{"start":140562180,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C"],"end":140562180,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1311384073","clinical_significance":[]},{"alleles":["C","T"],"end":140562183,"strand":1,"feature_type":"variation","start":140562183,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs963677857","clinical_significance":[]},{"seq_region_name":"7","id":"rs955082454","clinical_significance":[],"start":140562184,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140562184,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs974033230","alleles":["G","A","T"],"end":140562185,"feature_type":"variation","strand":1,"source":"dbSNP","start":140562185,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs114777084","feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140562188,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562188},{"id":"rs950344556","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140562189,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562189,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140562191,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562191,"source":"dbSNP","seq_region_name":"7","id":"rs958292029","clinical_significance":[]},{"seq_region_name":"7","id":"rs1401359203","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140562205,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562205,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585637791","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562206,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140562206},{"seq_region_name":"7","id":"rs989663234","clinical_significance":[],"alleles":["C","A"],"end":140562207,"strand":1,"feature_type":"variation","start":140562207,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140562208,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562208,"clinical_significance":[],"id":"rs1585637804","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1157406439","source":"dbSNP","start":140562209,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140562209,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1797645332","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562210,"source":"dbSNP","strand":1,"feature_type":"variation","end":140562210,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1169962286","clinical_significance":[],"start":140562211,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140562211,"alleles":["T","G"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140562217,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140562217,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797645543"},{"alleles":["A","C","G"],"end":140562218,"feature_type":"variation","strand":1,"source":"dbSNP","start":140562218,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1407122460","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140562249,"alleles":["TGGCAAGCCAGCAGTCCTGT","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562230,"clinical_significance":[],"seq_region_name":"7","id":"rs1478799495"},{"end":140562238,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140562238,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1797645934","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140562241,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140562241,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1797646030","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562242,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140562242,"clinical_significance":[],"seq_region_name":"7","id":"rs987257326"},{"clinical_significance":[],"id":"rs911636163","seq_region_name":"7","end":140562244,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140562244,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1488341425","feature_type":"variation","strand":1,"end":140562245,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562245},{"clinical_significance":[],"seq_region_name":"7","id":"rs943078593","alleles":["T","C"],"end":140562247,"feature_type":"variation","strand":1,"source":"dbSNP","start":140562247,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs566941923","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562248,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140562248},{"seq_region_name":"7","id":"rs1470800985","clinical_significance":[],"end":140562251,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140562251,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs945714442","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562252,"feature_type":"variation","strand":1,"alleles":["ACT","-"],"end":140562254},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562252,"source":"dbSNP","strand":1,"feature_type":"variation","end":140562257,"alleles":["ACTGCT","-"],"seq_region_name":"7","id":"rs1797646912","clinical_significance":[]},{"source":"dbSNP","start":140562255,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140562255,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1038886545"},{"seq_region_name":"7","id":"rs1279048371","clinical_significance":[],"start":140562263,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140562263,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs925748676","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140562269,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562269,"source":"dbSNP"},{"end":140562270,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140562270,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs928396759"},{"source":"dbSNP","start":140562273,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140562273,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1405172050","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1274496031","clinical_significance":[],"end":140562280,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140562280,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs935963057","seq_region_name":"7","alleles":["C","T"],"end":140562288,"feature_type":"variation","strand":1,"source":"dbSNP","start":140562288,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140562289,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562289,"source":"dbSNP","id":"rs1797647759","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140562290,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562290,"clinical_significance":[],"seq_region_name":"7","id":"rs528028065"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562291,"feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140562291,"clinical_significance":[],"seq_region_name":"7","id":"rs1797648081"},{"strand":1,"feature_type":"variation","end":140562296,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562296,"source":"dbSNP","id":"rs1797648298","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797648388","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562297,"feature_type":"variation","strand":1,"end":140562297,"alleles":["A","G"]},{"end":140562304,"alleles":["AGAGAGAG","AGAGAG","AGAGAGAGAG"],"strand":1,"feature_type":"variation","start":140562297,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs762532147","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140562300,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562300,"clinical_significance":[],"id":"rs1376659042","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562302,"source":"dbSNP","strand":1,"feature_type":"variation","end":140562302,"alleles":["G","A"],"seq_region_name":"7","id":"rs1797648732","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140562304,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562304,"source":"dbSNP","id":"rs755250011","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562305,"feature_type":"variation","strand":1,"end":140562305,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1797648951"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1178685394","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562309,"feature_type":"variation","strand":1,"end":140562309,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs540504402","end":140562310,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140562310,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["T","A"],"end":140562311,"strand":1,"feature_type":"variation","start":140562311,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1413127527","clinical_significance":[]},{"clinical_significance":[],"id":"rs1797649361","seq_region_name":"7","source":"dbSNP","start":140562313,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140562313,"alleles":["T","G"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140562318,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562318,"source":"dbSNP","id":"rs1797649466","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797649585","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562325,"source":"dbSNP","strand":1,"feature_type":"variation","end":140562325,"alleles":["T","C"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562331,"feature_type":"variation","strand":1,"end":140562331,"alleles":["G","A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1052948896"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797649840","feature_type":"variation","strand":1,"end":140562334,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562334},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140562335,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562335,"clinical_significance":[],"seq_region_name":"7","id":"rs188991839"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562335,"source":"dbSNP","strand":1,"feature_type":"variation","end":140562357,"alleles":["CAGAGCACCAGACTGATTGTTTC","C"],"id":"rs1797650059","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs892508369","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562336,"feature_type":"variation","strand":1,"end":140562336,"alleles":["A","C"]},{"end":140562339,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140562339,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs571557583"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1359188131","end":140562342,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140562342,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140562344,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140562344,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs781072851","clinical_significance":[]},{"seq_region_name":"7","id":"rs1190944307","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140562351,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562351,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585638155","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562354,"feature_type":"variation","strand":1,"end":140562354,"alleles":["T","C"]},{"strand":1,"feature_type":"variation","end":140562357,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562357,"source":"dbSNP","id":"rs1797651293","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562359,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140562359,"seq_region_name":"7","id":"rs1046350518","clinical_significance":[]},{"clinical_significance":[],"id":"rs1585638174","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562360,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140562360},{"alleles":["C","A"],"end":140562361,"strand":1,"feature_type":"variation","start":140562361,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1797651645","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562363,"feature_type":"variation","strand":1,"end":140562363,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1797651762"},{"id":"rs1797651873","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140562370,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562370,"source":"dbSNP"},{"start":140562371,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140562371,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797651989","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1301449716","feature_type":"variation","strand":1,"end":140562374,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562374},{"clinical_significance":[],"seq_region_name":"7","id":"rs993507230","feature_type":"variation","strand":1,"alleles":["C","A","G"],"end":140562376,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562376},{"id":"rs1310241126","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140562378,"alleles":["T","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562378,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562380,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140562380,"clinical_significance":[],"id":"rs1278134937","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1219443397","alleles":["C","T"],"end":140562381,"feature_type":"variation","strand":1,"source":"dbSNP","start":140562381,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1585638229","clinical_significance":[],"alleles":["T","G"],"end":140562382,"strand":1,"feature_type":"variation","start":140562382,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562387,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140562387,"clinical_significance":[],"seq_region_name":"7","id":"rs1320331570"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562388,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140562388,"seq_region_name":"7","id":"rs538552644","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562389,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140562389,"id":"rs1002673659","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562391,"feature_type":"variation","strand":1,"end":140562391,"alleles":["G","A"],"clinical_significance":[],"id":"rs1380444116","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562395,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140562395,"clinical_significance":[],"seq_region_name":"7","id":"rs890549961"},{"seq_region_name":"7","id":"rs879543211","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562397,"source":"dbSNP","strand":1,"feature_type":"variation","end":140562397,"alleles":["C","T"]},{"start":140562399,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140562399,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs963865681","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562400,"source":"dbSNP","strand":1,"feature_type":"variation","end":140562400,"alleles":["G","A"],"seq_region_name":"7","id":"rs995122538","clinical_significance":[]},{"id":"rs1797656253","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562402,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140562402},{"clinical_significance":[],"id":"rs1797656448","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140562403,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562403},{"start":140562406,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140562406,"alleles":["A","T"],"strand":1,"feature_type":"variation","id":"rs1797656641","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140562408,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140562408,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1017741877"},{"strand":1,"feature_type":"variation","end":140562409,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562409,"source":"dbSNP","id":"rs1425405165","seq_region_name":"7","clinical_significance":[]},{"start":140562411,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["-","TGAGCCTGTAAGTGGCT"],"end":140562410,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1477215243","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140562413,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562413,"source":"dbSNP","id":"rs1414372387","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562415,"feature_type":"variation","strand":1,"alleles":["A","-"],"end":140562415,"clinical_significance":[],"id":"rs1797657463","seq_region_name":"7"},{"seq_region_name":"7","id":"rs958177784","clinical_significance":[],"alleles":["C","T"],"end":140562416,"strand":1,"feature_type":"variation","start":140562416,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797657741","source":"dbSNP","start":140562419,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140562419,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797657891","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562422,"feature_type":"variation","strand":1,"end":140562422,"alleles":["G","A"]},{"start":140562426,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","G","T"],"end":140562426,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1217070718","clinical_significance":[]},{"clinical_significance":[],"id":"rs1026564166","seq_region_name":"7","source":"dbSNP","start":140562427,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140562427,"alleles":["T","A","C"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562432,"source":"dbSNP","strand":1,"feature_type":"variation","end":140562432,"alleles":["C","T"],"seq_region_name":"7","id":"rs950396797","clinical_significance":[]},{"seq_region_name":"7","id":"rs987142616","clinical_significance":[],"start":140562433,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140562433,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs2130579448","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562433,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GGG","GGGGGG","GGGGGGG"],"end":140562435},{"seq_region_name":"7","id":"rs1797658907","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562434,"source":"dbSNP","strand":1,"feature_type":"variation","end":140562434,"alleles":["G","A"]},{"id":"rs1395815222","seq_region_name":"7","clinical_significance":[],"start":140562436,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140562436,"alleles":["C","G","T"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562437,"source":"dbSNP","strand":1,"feature_type":"variation","end":140562437,"alleles":["G","A"],"seq_region_name":"7","id":"rs557146028","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797659528","clinical_significance":[],"strand":1,"feature_type":"variation","end":140562438,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562438,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585638425","source":"dbSNP","start":140562439,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140562439,"alleles":["A","G"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562440,"feature_type":"variation","strand":1,"end":140562440,"alleles":["T","G"],"clinical_significance":[],"id":"rs1585638427","seq_region_name":"7"},{"seq_region_name":"7","id":"rs964506652","clinical_significance":[],"end":140562443,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140562443,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140562444,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562444,"source":"dbSNP","seq_region_name":"7","id":"rs568926251","clinical_significance":[]},{"alleles":["A","G"],"end":140562445,"strand":1,"feature_type":"variation","start":140562445,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797660434","clinical_significance":[]},{"start":140562446,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140562446,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1174605735","clinical_significance":[]},{"alleles":["G","A","T"],"end":140562447,"strand":1,"feature_type":"variation","start":140562447,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs925832622","clinical_significance":[]},{"clinical_significance":[],"id":"rs941276221","seq_region_name":"7","source":"dbSNP","start":140562448,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140562448,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140562450,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A","C"],"end":140562450,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1401093672","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562454,"source":"dbSNP","strand":1,"feature_type":"variation","end":140562454,"alleles":["G","A"],"id":"rs1797661327","seq_region_name":"7","clinical_significance":[]},{"id":"rs536766935","seq_region_name":"7","clinical_significance":[],"end":140562457,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140562457,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs199910811","clinical_significance":[],"start":140562458,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C"],"end":140562458,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1797661980","clinical_significance":[],"alleles":["GAGA","GAGAGA"],"end":140562461,"strand":1,"feature_type":"variation","start":140562458,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["-","C"],"end":140562460,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562461,"source":"dbSNP","seq_region_name":"7","id":"rs1797662135","clinical_significance":[]},{"source":"dbSNP","start":140562461,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140562461,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs913161657"},{"alleles":["C","T"],"end":140562462,"feature_type":"variation","strand":1,"source":"dbSNP","start":140562462,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797662302"},{"strand":1,"feature_type":"variation","end":140562463,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562463,"source":"dbSNP","id":"rs1166351696","seq_region_name":"7","clinical_significance":[]},{"start":140562465,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140562465,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797662654","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs991206957","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562470,"feature_type":"variation","strand":1,"end":140562470,"alleles":["G","A"]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140562475,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562475,"clinical_significance":[],"seq_region_name":"7","id":"rs555054695"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562476,"source":"dbSNP","strand":1,"feature_type":"variation","end":140562476,"alleles":["A","G"],"seq_region_name":"7","id":"rs1178950347","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562477,"source":"dbSNP","strand":1,"feature_type":"variation","end":140562477,"alleles":["T","C"],"id":"rs941822382","seq_region_name":"7","clinical_significance":[]},{"end":140562480,"alleles":["T","C","G"],"strand":1,"feature_type":"variation","start":140562480,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs192616901","seq_region_name":"7","clinical_significance":[]},{"id":"rs1797663784","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562484,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140562484},{"clinical_significance":[],"id":"rs1797663955","seq_region_name":"7","source":"dbSNP","start":140562485,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140562485,"alleles":["C","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1282295364","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562488,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140562488},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140562489,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562489,"clinical_significance":[],"seq_region_name":"7","id":"rs906496485"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1284714878","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562490,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140562490},{"clinical_significance":[],"seq_region_name":"7","id":"rs1267282496","source":"dbSNP","start":140562493,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","G"],"end":140562493,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140562495,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140562495,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1219544792"},{"alleles":["C","A","T"],"end":140562496,"feature_type":"variation","strand":1,"source":"dbSNP","start":140562496,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797665248"},{"strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140562497,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562497,"source":"dbSNP","id":"rs919180922","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140562502,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562502,"clinical_significance":[],"id":"rs1797665743","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1242703332","alleles":["T","C","G"],"end":140562503,"feature_type":"variation","strand":1,"source":"dbSNP","start":140562503,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","T"],"end":140562505,"feature_type":"variation","strand":1,"source":"dbSNP","start":140562505,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs184775034"},{"source":"dbSNP","start":140562506,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140562512,"alleles":["AAAAAAA","AAAAAAAA"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797666303"},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140562509,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562509,"clinical_significance":[],"seq_region_name":"7","id":"rs186531549"},{"seq_region_name":"7","id":"rs1007617801","clinical_significance":[],"strand":1,"feature_type":"variation","end":140562519,"alleles":["ATTAGCTG","ATTAGCTGATTAGCTG"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562512,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797666891","source":"dbSNP","start":140562515,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140562515,"alleles":["A","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1797667073","clinical_significance":[],"start":140562516,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140562516,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562517,"feature_type":"variation","strand":1,"end":140562517,"alleles":["C","G"],"clinical_significance":[],"id":"rs1797667223","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562518,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140562518,"seq_region_name":"7","id":"rs1797667378","clinical_significance":[]},{"end":140562520,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140562520,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1390440017","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1039077104","source":"dbSNP","start":140562521,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140562521,"alleles":["G","A"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562522,"feature_type":"variation","strand":1,"end":140562522,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1294771725"},{"alleles":["G","A"],"end":140562523,"strand":1,"feature_type":"variation","start":140562523,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797668129","clinical_significance":[]},{"seq_region_name":"7","id":"rs1286890042","clinical_significance":[],"strand":1,"feature_type":"variation","end":140562525,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562525,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140562530,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562530,"source":"dbSNP","id":"rs899369544","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140562531,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562531,"source":"dbSNP","seq_region_name":"7","id":"rs994995461","clinical_significance":[]},{"end":140562533,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140562533,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797668827"},{"seq_region_name":"7","id":"rs1215794336","clinical_significance":[],"alleles":["T","C","G"],"end":140562534,"strand":1,"feature_type":"variation","start":140562534,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1585638743","clinical_significance":[],"start":140562535,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140562535,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562536,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140562536,"id":"rs1585638750","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797669502","clinical_significance":[],"end":140562540,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140562540,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs894006262","clinical_significance":[],"end":140562542,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140562542,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs199663825","seq_region_name":"7","end":140562544,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140562544,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797670110","alleles":["G","A"],"end":140562548,"feature_type":"variation","strand":1,"source":"dbSNP","start":140562548,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140562550,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562550,"source":"dbSNP","seq_region_name":"7","id":"rs1797670302","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585638776","clinical_significance":[],"strand":1,"feature_type":"variation","end":140562555,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562555,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1011021155","clinical_significance":[],"end":140562562,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","start":140562562,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140562563,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140562563,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797670891"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562564,"feature_type":"variation","strand":1,"end":140562564,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1026451213"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562565,"feature_type":"variation","strand":1,"end":140562565,"alleles":["G","A"],"clinical_significance":[],"id":"rs1189488203","seq_region_name":"7"},{"end":140562568,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140562568,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs886693239"},{"feature_type":"variation","strand":1,"end":140562570,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562570,"clinical_significance":[],"seq_region_name":"7","id":"rs1009125301"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140562578,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562578,"source":"dbSNP","seq_region_name":"7","id":"rs372820142","clinical_significance":[]},{"start":140562579,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140562579,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1018651027","clinical_significance":[]},{"source":"dbSNP","start":140562583,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140562583,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1268480568"},{"seq_region_name":"7","id":"rs964714469","clinical_significance":[],"alleles":["C","T"],"end":140562586,"strand":1,"feature_type":"variation","start":140562586,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140562587,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562587,"source":"dbSNP","seq_region_name":"7","id":"rs974559466","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1234505803","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562590,"feature_type":"variation","strand":1,"end":140562590,"alleles":["A","G"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562597,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140562597,"clinical_significance":[],"seq_region_name":"7","id":"rs1160096494"},{"clinical_significance":[],"id":"rs577496822","seq_region_name":"7","source":"dbSNP","start":140562598,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140562598,"alleles":["C","G","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs957111315","source":"dbSNP","start":140562603,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140562603,"alleles":["A","C","G"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140562607,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562607,"clinical_significance":[],"seq_region_name":"7","id":"rs988609397"},{"seq_region_name":"7","id":"rs1384520372","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140562609,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562609,"source":"dbSNP"},{"end":140562610,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140562610,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs913045636"},{"feature_type":"variation","strand":1,"end":140562616,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562616,"clinical_significance":[],"id":"rs949981647","seq_region_name":"7"},{"alleles":["T","C"],"end":140562618,"feature_type":"variation","strand":1,"source":"dbSNP","start":140562618,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs544564149"},{"end":140562620,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140562620,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1401745953"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1004168317","alleles":["C","A","G","T"],"end":140562621,"feature_type":"variation","strand":1,"source":"dbSNP","start":140562621,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs981309785","clinical_significance":[],"start":140562622,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140562622,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140562624,"alleles":["A","C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562624,"clinical_significance":[],"seq_region_name":"7","id":"rs1681794"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797674867","feature_type":"variation","strand":1,"end":140562625,"alleles":["G","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562625},{"seq_region_name":"7","id":"rs1797675091","clinical_significance":[],"start":140562630,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140562630,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140562632,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562632,"clinical_significance":[],"seq_region_name":"7","id":"rs1797675265"},{"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140562634,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562634,"clinical_significance":[],"seq_region_name":"7","id":"rs938007044"},{"end":140562638,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140562638,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1366870013"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562641,"source":"dbSNP","strand":1,"feature_type":"variation","end":140562641,"alleles":["G","A"],"seq_region_name":"7","id":"rs1797675878","clinical_significance":[]},{"clinical_significance":[],"id":"rs1681795","seq_region_name":"7","source":"dbSNP","start":140562643,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","G","T"],"end":140562643,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs542314229","end":140562644,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140562644,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140562646,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562646,"clinical_significance":[],"id":"rs560609669","seq_region_name":"7"},{"end":140562648,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140562648,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797676781"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562650,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140562650,"seq_region_name":"7","id":"rs546107274","clinical_significance":[]},{"start":140562653,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140562653,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797677136","clinical_significance":[]},{"id":"rs1261648238","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562655,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140562655},{"clinical_significance":[],"id":"rs528163881","seq_region_name":"7","alleles":["C","T"],"end":140562656,"feature_type":"variation","strand":1,"source":"dbSNP","start":140562656,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1335997172","clinical_significance":[],"start":140562657,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140562657,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140562657,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","-"],"end":140562657,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797677597"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1484457287","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562661,"feature_type":"variation","strand":1,"end":140562669,"alleles":["CAAAACAAA","CAAA"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562663,"feature_type":"variation","strand":1,"alleles":["A","ACA"],"end":140562663,"clinical_significance":[],"seq_region_name":"7","id":"rs2130580261"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562663,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AA","AACAA"],"end":140562664,"seq_region_name":"7","id":"rs2130580273","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562663,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AAACAAACAAACAAA","AAACAAACAAA","AAACAAACAAACAAACAAA","AAACAAACAAACAAACAAACAAA"],"end":140562677,"seq_region_name":"7","id":"rs112941923","clinical_significance":[]},{"clinical_significance":[],"id":"rs1585639160","seq_region_name":"7","source":"dbSNP","start":140562668,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AAC","AACTAAC"],"end":140562670,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140562671,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140562670,"alleles":["-","CAAA"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs386411501","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1278267663","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562671,"feature_type":"variation","strand":1,"end":140562671,"alleles":["A","G"]},{"source":"dbSNP","start":140562676,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140562676,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585639190"},{"seq_region_name":"7","id":"rs568405263","clinical_significance":[],"end":140562677,"alleles":["A","ACAAAACA","ACACA"],"strand":1,"feature_type":"variation","start":140562677,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1554468990","source":"dbSNP","start":140562677,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140562690,"alleles":["AACAACAACAACAA","AACAACAACAA","AACAACAACAACAACAA"],"feature_type":"variation","strand":1},{"id":"rs58292847","seq_region_name":"7","clinical_significance":[],"alleles":["-","C","CAAC","CAAG"],"end":140562677,"strand":1,"feature_type":"variation","start":140562678,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs199769924","end":140562678,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140562678,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1554468992","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["AC","CAA"],"end":140562679,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562678,"source":"dbSNP"},{"start":140562679,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140562679,"alleles":["C","A"],"strand":1,"feature_type":"variation","id":"rs200629116","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1300913586","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140562682,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562682,"source":"dbSNP"},{"alleles":["A","G"],"end":140562684,"strand":1,"feature_type":"variation","start":140562684,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1469468472","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140562688,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562688,"clinical_significance":[],"seq_region_name":"7","id":"rs866566897"},{"start":140562689,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AAAAAAA","AAAAAA","AAAAAAAA","AAAAAAAAA","AAAAAAAAAA","AAAAAAAAAAA"],"end":140562695,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1554468997","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562691,"source":"dbSNP","strand":1,"feature_type":"variation","end":140562691,"alleles":["A","C"],"seq_region_name":"7","id":"rs191322689","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs80018764","source":"dbSNP","start":140562695,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140562695,"alleles":["A","C"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562696,"feature_type":"variation","strand":1,"alleles":["-","AC"],"end":140562695,"clinical_significance":[],"seq_region_name":"7","id":"rs1554468998"},{"alleles":["CCC","CCCC","CCCCC"],"end":140562698,"feature_type":"variation","strand":1,"source":"dbSNP","start":140562696,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs142896649"},{"clinical_significance":[],"seq_region_name":"7","id":"rs866605491","source":"dbSNP","start":140562698,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140562698,"alleles":["C","A","T"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562699,"source":"dbSNP","strand":1,"feature_type":"variation","end":140562699,"alleles":["G","A"],"seq_region_name":"7","id":"rs564703873","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562705,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140562705,"clinical_significance":[],"seq_region_name":"7","id":"rs1019612700"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562706,"feature_type":"variation","strand":1,"end":140562706,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs532454167"},{"seq_region_name":"7","id":"rs550573945","clinical_significance":[],"alleles":["A","G"],"end":140562708,"strand":1,"feature_type":"variation","start":140562708,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797680933","source":"dbSNP","start":140562710,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140562710,"alleles":["G","C"],"feature_type":"variation","strand":1},{"start":140562714,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140562714,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1291236010","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562717,"source":"dbSNP","strand":1,"feature_type":"variation","end":140562717,"alleles":["C","G"],"seq_region_name":"7","id":"rs2130580516","clinical_significance":[]},{"end":140562719,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140562719,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1269116785","clinical_significance":[]},{"alleles":["A","-"],"end":140562720,"strand":1,"feature_type":"variation","start":140562720,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs774533513","seq_region_name":"7","clinical_significance":[]},{"start":140562721,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140562721,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs1342251879","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs373728293","clinical_significance":[],"end":140562722,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140562722,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797681621","source":"dbSNP","start":140562726,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140562726,"alleles":["G","C"],"feature_type":"variation","strand":1},{"start":140562727,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140562727,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585639491","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797681846","end":140562737,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140562737,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs996255129","clinical_significance":[],"end":140562738,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140562738,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1797682301","clinical_significance":[],"alleles":["GCCATGGGGTGCCA","GCCA"],"end":140562756,"strand":1,"feature_type":"variation","start":140562743,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs943361192","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140562744,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562744},{"start":140562747,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140562747,"alleles":["T","-"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797682685","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797682871","alleles":["G","A"],"end":140562748,"feature_type":"variation","strand":1,"source":"dbSNP","start":140562748,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs760493775","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562748,"feature_type":"variation","strand":1,"end":140562751,"alleles":["GGGG","GGG"]},{"id":"rs2130580644","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140562749,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562749,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1032642669","clinical_significance":[],"start":140562751,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140562751,"strand":1,"feature_type":"variation"},{"id":"rs569076379","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140562752,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562752,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140562758,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562758,"source":"dbSNP","seq_region_name":"7","id":"rs1797683458","clinical_significance":[]},{"clinical_significance":[],"id":"rs536412275","seq_region_name":"7","end":140562759,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140562759,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140562761,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140562761,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797683681"},{"seq_region_name":"7","id":"rs1387021470","clinical_significance":[],"end":140562763,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140562763,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140562765,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140562765,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1367307962","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs184699110","alleles":["G","A","C"],"end":140562768,"feature_type":"variation","strand":1,"source":"dbSNP","start":140562768,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140562776,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140562776,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1183303912"},{"end":140562787,"alleles":["CAATCAATC","CAATC"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140562779,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1797684255","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562779,"source":"dbSNP","strand":1,"feature_type":"variation","end":140562798,"alleles":["CAATCAATCGGTAAAACACA","CA"],"seq_region_name":"7","id":"rs1797684366","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1010905009","source":"dbSNP","start":140562780,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140562780,"alleles":["A","T"],"feature_type":"variation","strand":1},{"id":"rs1797684600","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562782,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140562782},{"start":140562785,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140562785,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs779048744","clinical_significance":[]},{"clinical_significance":[],"id":"rs1797684812","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562787,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140562787},{"seq_region_name":"7","id":"rs567019989","clinical_significance":[],"end":140562788,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140562788,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562791,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140562791,"seq_region_name":"7","id":"rs2930324","clinical_significance":[]},{"id":"rs1797685157","seq_region_name":"7","clinical_significance":[],"start":140562798,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140562798,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140562815,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562815,"source":"dbSNP","seq_region_name":"7","id":"rs1797685264","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140562818,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562818,"clinical_significance":[],"seq_region_name":"7","id":"rs902651468"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562819,"feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140562819,"clinical_significance":[],"id":"rs1003815538","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1797685667","seq_region_name":"7","feature_type":"variation","strand":1,"end":140562821,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562821},{"strand":1,"feature_type":"variation","end":140562824,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562824,"source":"dbSNP","id":"rs1797685783","seq_region_name":"7","clinical_significance":[]},{"end":140562826,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140562826,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1396677242","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797685993","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562828,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140562828},{"end":140562830,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140562830,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs564480481"},{"id":"rs1797686222","seq_region_name":"7","clinical_significance":[],"end":140562831,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140562831,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140562832,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140562832,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797686340","clinical_significance":[]},{"seq_region_name":"7","id":"rs895511478","clinical_significance":[],"strand":1,"feature_type":"variation","end":140562841,"alleles":["TTCTTCTTC","TTCTTC"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562833,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797686577","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140562834,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562834},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562835,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140562835,"clinical_significance":[],"seq_region_name":"7","id":"rs1937610471"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562836,"feature_type":"variation","strand":1,"end":140562836,"alleles":["T","C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1797686684"},{"alleles":["T","C"],"end":140562837,"strand":1,"feature_type":"variation","start":140562837,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797686813","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797686928","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562838,"source":"dbSNP","strand":1,"feature_type":"variation","end":140562838,"alleles":["C","T"]},{"id":"rs189782956","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140562839,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562839,"source":"dbSNP"},{"alleles":["A","G"],"end":140562844,"feature_type":"variation","strand":1,"source":"dbSNP","start":140562844,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs927193601"},{"feature_type":"variation","strand":1,"end":140562851,"alleles":["AATAAATA","AATA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562844,"clinical_significance":[],"seq_region_name":"7","id":"rs2130580947"},{"strand":1,"feature_type":"variation","end":140562845,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562845,"source":"dbSNP","id":"rs528450506","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1244911825","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140562850,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562850},{"seq_region_name":"7","id":"rs1377405786","clinical_significance":[],"start":140562851,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140562851,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140562859,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562859,"clinical_significance":[],"seq_region_name":"7","id":"rs1311238374"},{"seq_region_name":"7","id":"rs1444812008","clinical_significance":[],"strand":1,"feature_type":"variation","end":140562862,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562862,"source":"dbSNP"},{"id":"rs2130580997","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140562863,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562863,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797687787","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140562865,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562865},{"clinical_significance":[],"seq_region_name":"7","id":"rs772029078","source":"dbSNP","start":140562867,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140562867,"alleles":["C","G","T"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562869,"feature_type":"variation","strand":1,"end":140562869,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1797688029"},{"seq_region_name":"7","id":"rs1324281969","clinical_significance":[],"alleles":["T","C"],"end":140562870,"strand":1,"feature_type":"variation","start":140562870,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["A","G"],"end":140562871,"strand":1,"feature_type":"variation","start":140562871,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1797688276","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562872,"source":"dbSNP","strand":1,"feature_type":"variation","end":140562872,"alleles":["T","G"],"id":"rs1797688386","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140562873,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562873,"source":"dbSNP","id":"rs1407163040","seq_region_name":"7","clinical_significance":[]},{"id":"rs550154046","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562877,"source":"dbSNP","strand":1,"feature_type":"variation","end":140562877,"alleles":["G","C"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562880,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140562880,"clinical_significance":[],"seq_region_name":"7","id":"rs775390325"},{"id":"rs746596873","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140562882,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562882,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797688909","end":140562884,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140562884,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140562885,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562885,"clinical_significance":[],"seq_region_name":"7","id":"rs1420874216"},{"clinical_significance":[],"id":"rs1047825333","seq_region_name":"7","source":"dbSNP","start":140562886,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140562886,"alleles":["T","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs768371030","seq_region_name":"7","source":"dbSNP","start":140562894,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140562894,"alleles":["C","T"],"feature_type":"variation","strand":1},{"start":140562895,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140562895,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs944849450","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562897,"source":"dbSNP","strand":1,"feature_type":"variation","end":140562897,"alleles":["T","C"],"id":"rs1231958510","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","G"],"end":140562905,"feature_type":"variation","strand":1,"source":"dbSNP","start":140562905,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797689476"},{"seq_region_name":"7","id":"rs1797689570","clinical_significance":[],"alleles":["A","C"],"end":140562909,"strand":1,"feature_type":"variation","start":140562909,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1585639848","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562914,"source":"dbSNP","strand":1,"feature_type":"variation","end":140562914,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1244491811","end":140562915,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140562915,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1797689879","seq_region_name":"7","source":"dbSNP","start":140562916,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140562916,"alleles":["T","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797689978","source":"dbSNP","start":140562917,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["GG","G"],"end":140562918,"feature_type":"variation","strand":1},{"id":"rs1040513200","seq_region_name":"7","clinical_significance":[],"end":140562919,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140562919,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562921,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140562921,"clinical_significance":[],"seq_region_name":"7","id":"rs1797690326"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562923,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140562923,"seq_region_name":"7","id":"rs2130581169","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140562927,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562927,"source":"dbSNP","id":"rs1797690478","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs900755506","feature_type":"variation","strand":1,"end":140562930,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562930},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562934,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140562934,"seq_region_name":"7","id":"rs1797690836","clinical_significance":[]},{"clinical_significance":[],"id":"rs1452855457","seq_region_name":"7","source":"dbSNP","start":140562935,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140562935,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562940,"feature_type":"variation","strand":1,"end":140562940,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs996421385"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562948,"feature_type":"variation","strand":1,"end":140562948,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1054544843"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562950,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140562950,"id":"rs892788671","seq_region_name":"7","clinical_significance":[]},{"start":140562953,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140562953,"strand":1,"feature_type":"variation","id":"rs1221615197","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1009963642","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562962,"feature_type":"variation","strand":1,"end":140562962,"alleles":["C","G"]},{"end":140562963,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140562963,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797692024"},{"start":140562964,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140562964,"strand":1,"feature_type":"variation","id":"rs1797692197","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs558945771","source":"dbSNP","start":140562968,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140562968,"alleles":["A","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585639965","feature_type":"variation","strand":1,"end":140562971,"alleles":["G","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562971},{"alleles":["C","A"],"end":140562981,"feature_type":"variation","strand":1,"source":"dbSNP","start":140562981,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1287880218"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797692665","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140562984,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140562984},{"strand":1,"feature_type":"variation","end":140562992,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140562992,"source":"dbSNP","id":"rs1585639996","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1221930751","source":"dbSNP","start":140562993,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140562993,"alleles":["A","C"],"feature_type":"variation","strand":1},{"end":140562995,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140562995,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797693161","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs377192405","alleles":["A","C"],"end":140562997,"feature_type":"variation","strand":1,"source":"dbSNP","start":140562997,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140562998,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140562998,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797693486","clinical_significance":[]},{"source":"dbSNP","start":140563004,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140563004,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1197752370","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1350147329","seq_region_name":"7","alleles":["G","T"],"end":140563007,"feature_type":"variation","strand":1,"source":"dbSNP","start":140563007,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1291614933","source":"dbSNP","start":140563014,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140563014,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1797694083","clinical_significance":[],"alleles":["C","A","T"],"end":140563018,"strand":1,"feature_type":"variation","start":140563018,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563020,"feature_type":"variation","strand":1,"alleles":["GGG","GG"],"end":140563022,"clinical_significance":[],"id":"rs1797694218","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs540061327","source":"dbSNP","start":140563022,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["GTGT","GT"],"end":140563025,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1797694453","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140563033,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563033},{"clinical_significance":[],"seq_region_name":"7","id":"rs1204074021","end":140563039,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140563039,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140563042,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140563042,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs987435143"},{"seq_region_name":"7","id":"rs1585640074","clinical_significance":[],"strand":1,"feature_type":"variation","end":140563044,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563044,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1244808207","clinical_significance":[],"start":140563047,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140563047,"alleles":["A","C","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1019987584","feature_type":"variation","strand":1,"end":140563054,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563054},{"end":140563056,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140563056,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797695037","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130581472","clinical_significance":[],"start":140563058,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140563058,"strand":1,"feature_type":"variation"},{"alleles":["TGAATGACTT","TGAATGACTTGAATGACTT"],"end":140563068,"feature_type":"variation","strand":1,"source":"dbSNP","start":140563059,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1797695140","seq_region_name":"7"},{"end":140563063,"alleles":["T","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140563063,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1401126640","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1797695376","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563071,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140563071},{"clinical_significance":[],"id":"rs1797695477","seq_region_name":"7","end":140563074,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140563074,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1585640122","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563077,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140563077},{"source":"dbSNP","start":140563079,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140563079,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs971236578"},{"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140563080,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563080,"source":"dbSNP","id":"rs1363079214","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1003126830","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563082,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140563082},{"seq_region_name":"7","id":"rs1296663837","clinical_significance":[],"start":140563085,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140563085,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs943411778","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140563086,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563086},{"seq_region_name":"7","id":"rs1797696191","clinical_significance":[],"start":140563087,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140563087,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1797696432","seq_region_name":"7","source":"dbSNP","start":140563091,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140563091,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1797696538","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["CAGCCAAGA","-"],"end":140563105,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563097,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563107,"source":"dbSNP","strand":1,"feature_type":"variation","end":140563107,"alleles":["T","C"],"id":"rs1797696640","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1406726193","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563112,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140563112},{"clinical_significance":[],"seq_region_name":"7","id":"rs150720453","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563114,"feature_type":"variation","strand":1,"end":140563114,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs77444529","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563119,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140563119},{"seq_region_name":"7","id":"rs775938738","clinical_significance":[],"start":140563125,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140563125,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"start":140563128,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140563128,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs1797697145","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs761381474","alleles":["A","G"],"end":140563130,"feature_type":"variation","strand":1,"source":"dbSNP","start":140563130,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563133,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140563133,"seq_region_name":"7","id":"rs1797697325","clinical_significance":[]},{"source":"dbSNP","start":140563134,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140563134,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797697420"},{"seq_region_name":"7","id":"rs1426564781","clinical_significance":[],"alleles":["G","A"],"end":140563135,"strand":1,"feature_type":"variation","start":140563135,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140563139,"alleles":["GTTTC","-"],"strand":1,"feature_type":"variation","start":140563135,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs200158827","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1182958657","end":140563141,"alleles":["GTTTCTC","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140563135,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs59090586","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563139,"source":"dbSNP","strand":1,"feature_type":"variation","end":140563139,"alleles":["C","T"]},{"id":"rs115291618","seq_region_name":"7","clinical_significance":[],"alleles":["T","A"],"end":140563140,"strand":1,"feature_type":"variation","start":140563140,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs116026833","clinical_significance":[],"strand":1,"feature_type":"variation","end":140563141,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563141,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1476123644","source":"dbSNP","start":140563142,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140563141,"alleles":["-","AA"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1585640314","seq_region_name":"7","alleles":["C","T"],"end":140563144,"feature_type":"variation","strand":1,"source":"dbSNP","start":140563144,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs974004401","source":"dbSNP","start":140563145,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140563145,"alleles":["A","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1585640327","clinical_significance":[],"start":140563146,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140563146,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140563148,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563148,"source":"dbSNP","seq_region_name":"7","id":"rs1797698594","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs920615835","alleles":["A","G"],"end":140563150,"feature_type":"variation","strand":1,"source":"dbSNP","start":140563150,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140563153,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563153,"clinical_significance":[],"seq_region_name":"7","id":"rs1279109466"},{"id":"rs1797699110","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563160,"source":"dbSNP","strand":1,"feature_type":"variation","end":140563160,"alleles":["C","T"]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140563163,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563163,"clinical_significance":[],"id":"rs939500569","seq_region_name":"7"},{"start":140563167,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140563167,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797699430","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797699584","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563173,"source":"dbSNP","strand":1,"feature_type":"variation","end":140563173,"alleles":["C","G"]},{"end":140563178,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140563178,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797699732","clinical_significance":[]},{"seq_region_name":"7","id":"rs952023414","clinical_significance":[],"alleles":["C","T"],"end":140563180,"strand":1,"feature_type":"variation","start":140563180,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140563181,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563181,"source":"dbSNP","seq_region_name":"7","id":"rs1797700069","clinical_significance":[]},{"id":"rs1797700227","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563187,"source":"dbSNP","strand":1,"feature_type":"variation","end":140563187,"alleles":["A","G"]},{"end":140563189,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140563189,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797700391","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797700535","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563193,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140563193},{"feature_type":"variation","strand":1,"end":140563195,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563195,"clinical_significance":[],"seq_region_name":"7","id":"rs181805322"},{"id":"rs1797700835","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140563200,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563200,"source":"dbSNP"},{"id":"rs1282717652","seq_region_name":"7","clinical_significance":[],"start":140563201,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140563201,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797700963","feature_type":"variation","strand":1,"end":140563206,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563206},{"feature_type":"variation","strand":1,"alleles":["CAGCCCAG","CAG"],"end":140563217,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563210,"clinical_significance":[],"seq_region_name":"7","id":"rs1585640401"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797701202","source":"dbSNP","start":140563213,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140563213,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140563219,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","G","T"],"end":140563219,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs983570462","seq_region_name":"7"},{"id":"rs1797701464","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140563223,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563223,"source":"dbSNP"},{"seq_region_name":"7","id":"rs547140216","clinical_significance":[],"start":140563226,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140563226,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"id":"rs1797701677","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140563230,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563230,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs944736271","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563232,"feature_type":"variation","strand":1,"end":140563232,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797701901","feature_type":"variation","strand":1,"end":140563234,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563234},{"start":140563235,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140563235,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1040962698","clinical_significance":[]},{"start":140563236,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140563236,"strand":1,"feature_type":"variation","id":"rs1022652797","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140563240,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563240,"clinical_significance":[],"seq_region_name":"7","id":"rs922098156"},{"start":140563242,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C","G"],"end":140563242,"strand":1,"feature_type":"variation","id":"rs932252769","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1585640454","seq_region_name":"7","source":"dbSNP","start":140563246,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140563246,"alleles":["C","A"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563251,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140563251,"clinical_significance":[],"seq_region_name":"7","id":"rs1797702589"},{"id":"rs1360079768","seq_region_name":"7","clinical_significance":[],"start":140563255,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140563255,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797702814","end":140563257,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140563257,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1336612850","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140563263,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563263},{"source":"dbSNP","start":140563268,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["ACAGGCACACTTGTGC","-"],"end":140563283,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1797703012","seq_region_name":"7"},{"source":"dbSNP","start":140563270,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140563270,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs542059345"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797703206","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563273,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140563273},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797703317","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140563277,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563277},{"seq_region_name":"7","id":"rs1403536112","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563280,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140563280},{"clinical_significance":[],"seq_region_name":"7","id":"rs139072444","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563283,"feature_type":"variation","strand":1,"end":140563283,"alleles":["C","G","T"]},{"source":"dbSNP","start":140563284,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140563284,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1451055785"},{"end":140563286,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140563286,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130582031"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563288,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140563288,"seq_region_name":"7","id":"rs1797703791","clinical_significance":[]},{"start":140563293,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140563293,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs185317787","clinical_significance":[]},{"end":140563294,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140563294,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs539934784","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130582065","end":140563300,"alleles":["TCATCA","TCATCATCA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140563295,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140563306,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563306,"source":"dbSNP","seq_region_name":"7","id":"rs1184670594","clinical_significance":[]},{"id":"rs1639945","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140563309,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563309,"source":"dbSNP"},{"seq_region_name":"7","id":"rs2130582103","clinical_significance":[],"alleles":["T","G"],"end":140563311,"strand":1,"feature_type":"variation","start":140563311,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1797704540","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["ATCA","A"],"end":140563315,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563312,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140563317,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563317,"source":"dbSNP","id":"rs766603756","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140563318,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563318,"source":"dbSNP","seq_region_name":"7","id":"rs1268579960","clinical_significance":[]},{"seq_region_name":"7","id":"rs551184427","clinical_significance":[],"strand":1,"feature_type":"variation","end":140563324,"alleles":["A","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563324,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130582155","source":"dbSNP","start":140563325,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140563325,"alleles":["T","A","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1797705307","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140563327,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563327,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563329,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140563329,"seq_region_name":"7","id":"rs950615666","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140563330,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563330,"clinical_significance":[],"id":"rs2130582183","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563335,"feature_type":"variation","strand":1,"end":140563335,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1797705474"},{"clinical_significance":[],"id":"rs1797705623","seq_region_name":"7","end":140563336,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140563336,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797705772","alleles":["T","C"],"end":140563341,"feature_type":"variation","strand":1,"source":"dbSNP","start":140563341,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1262766765","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563342,"source":"dbSNP","strand":1,"feature_type":"variation","end":140563342,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1797706108","clinical_significance":[],"strand":1,"feature_type":"variation","end":140563343,"alleles":["C","A","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563343,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140563344,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563344,"clinical_significance":[],"seq_region_name":"7","id":"rs987708226"},{"end":140563345,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140563345,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797706513","clinical_significance":[]},{"seq_region_name":"7","id":"rs750209812","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563348,"source":"dbSNP","strand":1,"feature_type":"variation","end":140563348,"alleles":["G","A"]},{"end":140563353,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140563353,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs2130582264","seq_region_name":"7"},{"id":"rs1797706838","seq_region_name":"7","clinical_significance":[],"start":140563362,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140563362,"strand":1,"feature_type":"variation"},{"alleles":["C","A","T"],"end":140563373,"strand":1,"feature_type":"variation","start":140563373,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs189391122","clinical_significance":[]},{"start":140563374,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140563374,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1639948","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797707529","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563379,"feature_type":"variation","strand":1,"end":140563379,"alleles":["T","G"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563380,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140563380,"clinical_significance":[],"seq_region_name":"7","id":"rs755087511"},{"id":"rs1214474328","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563386,"source":"dbSNP","strand":1,"feature_type":"variation","end":140563386,"alleles":["C","G"]},{"id":"rs1380604495","seq_region_name":"7","clinical_significance":[],"end":140563396,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140563396,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1797708040","clinical_significance":[],"alleles":["T","A"],"end":140563399,"strand":1,"feature_type":"variation","start":140563399,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140563400,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140563400,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797708139"},{"feature_type":"variation","strand":1,"end":140563406,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563406,"clinical_significance":[],"id":"rs1797708239","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1286319379","seq_region_name":"7","end":140563407,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140563407,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1797708488","clinical_significance":[],"strand":1,"feature_type":"variation","end":140563410,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563410,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140563413,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563413,"source":"dbSNP","seq_region_name":"7","id":"rs1450923213","clinical_significance":[]},{"id":"rs767843656","seq_region_name":"7","clinical_significance":[],"start":140563417,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140563417,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140563422,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140563422,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1034609821"},{"source":"dbSNP","start":140563426,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140563426,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs73491576"},{"feature_type":"variation","strand":1,"end":140563431,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563431,"clinical_significance":[],"seq_region_name":"7","id":"rs1797708967"},{"seq_region_name":"7","id":"rs1262385286","clinical_significance":[],"end":140563434,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140563434,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1355746606","feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140563435,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563435},{"strand":1,"feature_type":"variation","end":140563437,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563437,"source":"dbSNP","seq_region_name":"7","id":"rs1448159349","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563440,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140563440,"clinical_significance":[],"seq_region_name":"7","id":"rs1585640870"},{"strand":1,"feature_type":"variation","end":140563450,"alleles":["A","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563450,"source":"dbSNP","seq_region_name":"7","id":"rs2130582451","clinical_significance":[]},{"alleles":["T","C"],"end":140563451,"feature_type":"variation","strand":1,"source":"dbSNP","start":140563451,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs995869016"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563454,"source":"dbSNP","strand":1,"feature_type":"variation","end":140563454,"alleles":["G","A"],"id":"rs1414448776","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs530016654","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563457,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140563457},{"clinical_significance":[],"seq_region_name":"7","id":"rs548436114","source":"dbSNP","start":140563459,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140563459,"feature_type":"variation","strand":1},{"start":140563465,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TTTT","TTTTT"],"end":140563468,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1442565400","clinical_significance":[]},{"seq_region_name":"7","id":"rs1242716634","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563469,"source":"dbSNP","strand":1,"feature_type":"variation","end":140563469,"alleles":["A","G"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563470,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140563470,"seq_region_name":"7","id":"rs951244165","clinical_significance":[]},{"id":"rs1249675431","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140563471,"strand":1,"feature_type":"variation","start":140563471,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140563473,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563473,"source":"dbSNP","seq_region_name":"7","id":"rs1204000602","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140563474,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563474,"clinical_significance":[],"seq_region_name":"7","id":"rs1797710426"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1322780114","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563475,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140563475},{"seq_region_name":"7","id":"rs75251202","clinical_significance":[],"strand":1,"feature_type":"variation","end":140563476,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563476,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1244182385","end":140563477,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140563477,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563479,"source":"dbSNP","strand":1,"feature_type":"variation","end":140563479,"alleles":["T","C"],"id":"rs1178190051","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1434838162","seq_region_name":"7","feature_type":"variation","strand":1,"end":140563481,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563481},{"seq_region_name":"7","id":"rs1797711214","clinical_significance":[],"start":140563483,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140563483,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["GGGG","GGG"],"end":140563495,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563492,"source":"dbSNP","id":"rs2130582584","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563495,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140563495,"clinical_significance":[],"seq_region_name":"7","id":"rs1431872795"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797711649","feature_type":"variation","strand":1,"end":140563496,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563496},{"id":"rs1310508026","seq_region_name":"7","clinical_significance":[],"end":140563498,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140563498,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1797711981","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140563499,"strand":1,"feature_type":"variation","start":140563499,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140563502,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140563502,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797712134","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585641047","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563505,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140563505},{"end":140563506,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140563506,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs939573196"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140563510,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563510,"clinical_significance":[],"seq_region_name":"7","id":"rs1797712655"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797712814","feature_type":"variation","strand":1,"alleles":["TT","T"],"end":140563518,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563517},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797712996","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563522,"feature_type":"variation","strand":1,"end":140563522,"alleles":["A","G"]},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140563524,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563524,"source":"dbSNP","seq_region_name":"7","id":"rs1468588514","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563525,"feature_type":"variation","strand":1,"end":140563525,"alleles":["A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1797713333"},{"source":"dbSNP","start":140563528,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140563528,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs534318316"},{"seq_region_name":"7","id":"rs1797713919","clinical_significance":[],"start":140563529,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140563529,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140563542,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140563542,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs35043414","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1172464294","clinical_significance":[],"alleles":["C","A","G"],"end":140563543,"strand":1,"feature_type":"variation","start":140563543,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797714455","alleles":["AAAAAAA","AAAAAA"],"end":140563550,"feature_type":"variation","strand":1,"source":"dbSNP","start":140563544,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1440855985","seq_region_name":"7","source":"dbSNP","start":140563548,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140563548,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1386332348","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563550,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140563550},{"id":"rs376166859","seq_region_name":"7","clinical_significance":[],"start":140563553,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140563553,"alleles":["T","G"],"strand":1,"feature_type":"variation"},{"end":140563556,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140563556,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797715071","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1165427140","source":"dbSNP","start":140563557,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140563557,"alleles":["A","T"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563564,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140563564,"clinical_significance":[],"seq_region_name":"7","id":"rs1797715366"},{"source":"dbSNP","start":140563566,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140563566,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs966541632"},{"clinical_significance":[],"seq_region_name":"7","id":"rs976183051","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563569,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140563569},{"seq_region_name":"7","id":"rs1797715860","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563570,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AGAAG","AG"],"end":140563574},{"clinical_significance":[],"seq_region_name":"7","id":"rs1056657114","alleles":["A","G"],"end":140563573,"feature_type":"variation","strand":1,"source":"dbSNP","start":140563573,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1384357155","feature_type":"variation","strand":1,"end":140563574,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563574},{"start":140563575,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140563575,"strand":1,"feature_type":"variation","id":"rs181838569","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140563585,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563585,"clinical_significance":[],"seq_region_name":"7","id":"rs1797716489"},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140563586,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563586,"source":"dbSNP","id":"rs1797716647","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1316309483","clinical_significance":[],"start":140563589,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140563589,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1339995017","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563592,"feature_type":"variation","strand":1,"end":140563592,"alleles":["T","A"]},{"source":"dbSNP","start":140563600,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140563600,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797717135"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140563606,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563606,"clinical_significance":[],"id":"rs922115162","seq_region_name":"7"},{"source":"dbSNP","start":140563608,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140563608,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1441775488"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797717599","feature_type":"variation","strand":1,"end":140563618,"alleles":["-","TG"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563619},{"id":"rs1797717771","seq_region_name":"7","clinical_significance":[],"start":140563621,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140563622,"alleles":["GA","GACCTACTTGAGGGTAGA"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563622,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140563622,"clinical_significance":[],"seq_region_name":"7","id":"rs932165361"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563624,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140563624,"clinical_significance":[],"seq_region_name":"7","id":"rs1797718108"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1248693122","alleles":["T","A"],"end":140563625,"feature_type":"variation","strand":1,"source":"dbSNP","start":140563625,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["AAAA","AAA"],"end":140563629,"strand":1,"feature_type":"variation","start":140563626,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797718455","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563629,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140563629,"id":"rs1176637344","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs537807944","clinical_significance":[],"start":140563633,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140563633,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797718942","source":"dbSNP","start":140563637,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140563637,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs990839485","feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140563638,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563638},{"id":"rs1797719310","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140563639,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563639,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797719468","feature_type":"variation","strand":1,"end":140563640,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563640},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563647,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140563647,"clinical_significance":[],"seq_region_name":"7","id":"rs1797719604"},{"seq_region_name":"7","id":"rs1314304730","clinical_significance":[],"start":140563649,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140563649,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1585641252","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563652,"source":"dbSNP","strand":1,"feature_type":"variation","end":140563652,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797720107","source":"dbSNP","start":140563655,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140563655,"alleles":["C","T"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140563659,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["GATGATCACCATTG","G"],"end":140563672,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1359425251"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1405759239","feature_type":"variation","strand":1,"alleles":["ATGATCAC","-"],"end":140563667,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563660},{"seq_region_name":"7","id":"rs1285456802","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140563661,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563661,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140563662,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563662,"clinical_significance":[],"id":"rs1797720798","seq_region_name":"7"},{"clinical_significance":[],"id":"rs2130583050","seq_region_name":"7","source":"dbSNP","start":140563665,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140563665,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140563667,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140563667,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs914832755"},{"start":140563668,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140563668,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1232271396","clinical_significance":[]},{"end":140563669,"alleles":["A","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140563669,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797721366"},{"end":140563670,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140563670,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1287182900","clinical_significance":[]},{"start":140563672,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["GCATTAAA","-"],"end":140563679,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1261175639","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797721925","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140563674,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563674,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1797722113","clinical_significance":[],"start":140563674,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140563677,"alleles":["ATTA","A"],"strand":1,"feature_type":"variation"},{"end":140563675,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140563675,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797722273"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563675,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TT","T"],"end":140563676,"seq_region_name":"7","id":"rs1797722382","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797722485","alleles":["TT","-"],"end":140563676,"feature_type":"variation","strand":1,"source":"dbSNP","start":140563675,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140563676,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140563676,"alleles":["T","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1318285551","clinical_significance":[]},{"start":140563676,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TAA","-"],"end":140563678,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1242769259","clinical_significance":[]},{"id":"rs1352732211","seq_region_name":"7","clinical_significance":[],"alleles":["A","T"],"end":140563677,"strand":1,"feature_type":"variation","start":140563677,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563677,"source":"dbSNP","strand":1,"feature_type":"variation","end":140563704,"alleles":["AAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAA","AAAAAAAAAAAAA","AAAAAAAAAAAAAA","AAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA"],"seq_region_name":"7","id":"rs139848094","clinical_significance":[]},{"clinical_significance":[],"id":"rs1797723630","seq_region_name":"7","feature_type":"variation","strand":1,"end":140563679,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563679},{"seq_region_name":"7","id":"rs1261795393","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563680,"source":"dbSNP","strand":1,"feature_type":"variation","end":140563680,"alleles":["A","T"]},{"feature_type":"variation","strand":1,"end":140563687,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563687,"clinical_significance":[],"seq_region_name":"7","id":"rs1797723825"},{"seq_region_name":"7","id":"rs946262686","clinical_significance":[],"end":140563689,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140563689,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140563691,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563691,"source":"dbSNP","seq_region_name":"7","id":"rs1797724030","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1490384114","source":"dbSNP","start":140563701,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140563701,"alleles":["A","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1201072697","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563703,"feature_type":"variation","strand":1,"end":140563703,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797724351","end":140563705,"alleles":["AAG","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140563703,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140563704,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563704,"clinical_significance":[],"seq_region_name":"7","id":"rs1797724447"},{"start":140563705,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C","T"],"end":140563705,"strand":1,"feature_type":"variation","id":"rs1266368358","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","-"],"end":140563705,"strand":1,"feature_type":"variation","start":140563705,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797724675","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1479622404","source":"dbSNP","start":140563706,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140563706,"alleles":["C","A"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["C","A","G"],"end":140563707,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563707,"clinical_significance":[],"id":"rs1198581300","seq_region_name":"7"},{"start":140563708,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140563708,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585641445","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797725112","clinical_significance":[],"alleles":["G","A"],"end":140563709,"strand":1,"feature_type":"variation","start":140563709,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs948304777","alleles":["A","C","T"],"end":140563712,"feature_type":"variation","strand":1,"source":"dbSNP","start":140563712,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs2130583320","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563716,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140563716},{"source":"dbSNP","start":140563720,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140563720,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130583325"},{"end":140563726,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140563726,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1364804897"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797725413","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563727,"feature_type":"variation","strand":1,"end":140563727,"alleles":["A","C"]},{"seq_region_name":"7","id":"rs1797725531","clinical_significance":[],"start":140563728,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","T"],"end":140563728,"strand":1,"feature_type":"variation"},{"id":"rs1797725637","seq_region_name":"7","clinical_significance":[],"start":140563731,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140563731,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563732,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140563732,"clinical_significance":[],"seq_region_name":"7","id":"rs1797725742"},{"strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140563734,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563734,"source":"dbSNP","seq_region_name":"7","id":"rs1797725855","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797725980","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140563736,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563736},{"seq_region_name":"7","id":"rs1797726081","clinical_significance":[],"end":140563737,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140563737,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140563739,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140563739,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1041382698"},{"strand":1,"feature_type":"variation","end":140563740,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563740,"source":"dbSNP","seq_region_name":"7","id":"rs1585641518","clinical_significance":[]},{"clinical_significance":[],"id":"rs555413901","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563743,"feature_type":"variation","strand":1,"end":140563743,"alleles":["G","A","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs938453468","source":"dbSNP","start":140563744,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140563744,"feature_type":"variation","strand":1},{"alleles":["C","T"],"end":140563753,"strand":1,"feature_type":"variation","start":140563753,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1312423311","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1425420003","end":140563754,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140563754,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1055547454","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140563756,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563756},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563762,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140563762,"clinical_significance":[],"seq_region_name":"7","id":"rs1305120729"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1221223514","source":"dbSNP","start":140563765,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140563765,"alleles":["G","T"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140563767,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563767,"clinical_significance":[],"seq_region_name":"7","id":"rs778960534"},{"id":"rs1797727189","seq_region_name":"7","clinical_significance":[],"start":140563768,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140563768,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140563771,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563771,"source":"dbSNP","id":"rs894334369","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1344786874","clinical_significance":[],"strand":1,"feature_type":"variation","end":140563772,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563772,"source":"dbSNP"},{"seq_region_name":"7","id":"rs995361175","clinical_significance":[],"strand":1,"feature_type":"variation","end":140563774,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563774,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563776,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140563776,"seq_region_name":"7","id":"rs533723125","clinical_significance":[]},{"id":"rs1797727715","seq_region_name":"7","clinical_significance":[],"end":140563778,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140563778,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140563786,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140563786,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797727824","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1383670850","feature_type":"variation","strand":1,"end":140563787,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563787},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797727963","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563789,"feature_type":"variation","strand":1,"alleles":["C","-"],"end":140563789},{"clinical_significance":[],"id":"rs1386476298","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563793,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140563793},{"source":"dbSNP","start":140563794,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140563794,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs568460877"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563795,"feature_type":"variation","strand":1,"end":140563795,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1288091557"},{"alleles":["AAGA","-"],"end":140563798,"feature_type":"variation","strand":1,"source":"dbSNP","start":140563795,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1307430749"},{"seq_region_name":"7","id":"rs1797728713","clinical_significance":[],"end":140563799,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140563799,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["C","T"],"end":140563802,"feature_type":"variation","strand":1,"source":"dbSNP","start":140563802,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1466688007","seq_region_name":"7"},{"seq_region_name":"7","id":"rs887044439","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563803,"source":"dbSNP","strand":1,"feature_type":"variation","end":140563803,"alleles":["G","A","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797729214","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140563806,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563806},{"clinical_significance":[],"seq_region_name":"7","id":"rs750350263","alleles":["C","A","T"],"end":140563810,"feature_type":"variation","strand":1,"source":"dbSNP","start":140563810,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1004106415","clinical_significance":[],"strand":1,"feature_type":"variation","end":140563811,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563811,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130583665","source":"dbSNP","start":140563813,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140563813,"alleles":["A","T"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563814,"feature_type":"variation","strand":1,"end":140563831,"alleles":["AAATAAATAAATAAATAA","AAATAAATAAATAA"],"clinical_significance":[],"id":"rs1797729608","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563818,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140563818,"clinical_significance":[],"id":"rs898860251","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797729813","feature_type":"variation","strand":1,"end":140563821,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563821},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140563823,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563823,"clinical_significance":[],"seq_region_name":"7","id":"rs994902963"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1427284144","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140563825,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563825},{"end":140563830,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140563830,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797730144"},{"seq_region_name":"7","id":"rs1797730244","clinical_significance":[],"start":140563833,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140563833,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs2130583740","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563834,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140563834},{"id":"rs1047514493","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563836,"source":"dbSNP","strand":1,"feature_type":"variation","end":140563836,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130583768","source":"dbSNP","start":140563837,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140563837,"alleles":["G","C"],"feature_type":"variation","strand":1},{"id":"rs1797730472","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563838,"source":"dbSNP","strand":1,"feature_type":"variation","end":140563838,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1201394567","clinical_significance":[],"start":140563841,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140563841,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs758437334","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563847,"source":"dbSNP","strand":1,"feature_type":"variation","end":140563847,"alleles":["A","G"]},{"end":140563850,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140563850,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs114892087","clinical_significance":[]},{"start":140563851,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140563851,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs186493214","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130583821","clinical_significance":[],"alleles":["C","G"],"end":140563853,"strand":1,"feature_type":"variation","start":140563853,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1289031972","seq_region_name":"7","source":"dbSNP","start":140563854,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140563854,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs189657176","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140563857,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563857},{"start":140563858,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140563858,"strand":1,"feature_type":"variation","id":"rs540326481","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs746827270","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563860,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140563860},{"source":"dbSNP","start":140563864,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","-"],"end":140563864,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs2130583861","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797731870","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563871,"feature_type":"variation","strand":1,"end":140563871,"alleles":["G","A"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563876,"feature_type":"variation","strand":1,"end":140563876,"alleles":["G","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs370455917"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797732095","source":"dbSNP","start":140563877,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140563877,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140563883,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140563883,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs10429043"},{"end":140563884,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140563884,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs953551699","clinical_significance":[]},{"seq_region_name":"7","id":"rs990279733","clinical_significance":[],"start":140563886,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140563886,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs2130583913","seq_region_name":"7","alleles":["G","T"],"end":140563890,"feature_type":"variation","strand":1,"source":"dbSNP","start":140563890,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1385239228","end":140563893,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140563893,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140563898,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563898,"clinical_significance":[],"seq_region_name":"7","id":"rs1469512056"},{"seq_region_name":"7","id":"rs1797732827","clinical_significance":[],"end":140563902,"alleles":["AGCC","-"],"strand":1,"feature_type":"variation","start":140563899,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs570133933","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140563900,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563900,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs576862340","end":140563904,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140563904,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs977630622","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563908,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140563908},{"clinical_significance":[],"seq_region_name":"7","id":"rs1683126347","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563909,"feature_type":"variation","strand":1,"end":140563909,"alleles":["G","A"]},{"id":"rs2130583976","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563910,"source":"dbSNP","strand":1,"feature_type":"variation","end":140563910,"alleles":["T","G"]},{"strand":1,"feature_type":"variation","end":140563914,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563914,"source":"dbSNP","id":"rs1373076465","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs928329024","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563918,"feature_type":"variation","strand":1,"end":140563918,"alleles":["G","T"]},{"seq_region_name":"7","id":"rs1797733462","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563928,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140563928},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563931,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140563931,"clinical_significance":[],"seq_region_name":"7","id":"rs1797733586"},{"seq_region_name":"7","id":"rs938352426","clinical_significance":[],"strand":1,"feature_type":"variation","end":140563933,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563933,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1055833331","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563934,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140563934},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797733772","source":"dbSNP","start":140563938,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140563938,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140563939,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563939,"clinical_significance":[],"id":"rs1585642020","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs961090171","source":"dbSNP","start":140563943,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140563943,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797734104","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563944,"feature_type":"variation","strand":1,"end":140563944,"alleles":["A","G"]},{"end":140563946,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140563946,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1460611890"},{"strand":1,"feature_type":"variation","end":140563947,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563947,"source":"dbSNP","seq_region_name":"7","id":"rs78821987","clinical_significance":[]},{"id":"rs1337357318","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563955,"source":"dbSNP","strand":1,"feature_type":"variation","end":140563955,"alleles":["G","A"]},{"id":"rs1457563547","seq_region_name":"7","clinical_significance":[],"start":140563957,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140563957,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs667416","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563963,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140563963},{"seq_region_name":"7","id":"rs1585642082","clinical_significance":[],"end":140563964,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140563964,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1245209865","source":"dbSNP","start":140563970,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["ACA","A"],"end":140563972,"feature_type":"variation","strand":1},{"id":"rs526070","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140563971,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563971,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563974,"feature_type":"variation","strand":1,"end":140563974,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1797735221"},{"seq_region_name":"7","id":"rs772729774","clinical_significance":[],"strand":1,"feature_type":"variation","end":140563978,"alleles":["C","A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563978,"source":"dbSNP"},{"source":"dbSNP","start":140563980,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140563980,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1563143955"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1377935889","alleles":["A","C"],"end":140563989,"feature_type":"variation","strand":1,"source":"dbSNP","start":140563989,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1797735635","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140563990,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140563990,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797735730","feature_type":"variation","strand":1,"end":140563993,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140563993},{"seq_region_name":"7","id":"rs1797735839","clinical_significance":[],"start":140563999,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140563999,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs542113518","clinical_significance":[],"start":140564005,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140564005,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797736062","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564007,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140564007},{"strand":1,"feature_type":"variation","end":140564010,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564010,"source":"dbSNP","seq_region_name":"7","id":"rs117681000","clinical_significance":[]},{"alleles":["G","A"],"end":140564012,"strand":1,"feature_type":"variation","start":140564012,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs568175578","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1396378582","source":"dbSNP","start":140564014,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140564014,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797736493","source":"dbSNP","start":140564015,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140564015,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797736590","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140564016,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564016},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140564017,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564017,"clinical_significance":[],"seq_region_name":"7","id":"rs1038668993"},{"end":140564020,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140564020,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797736801"},{"seq_region_name":"7","id":"rs1164380658","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564022,"source":"dbSNP","strand":1,"feature_type":"variation","end":140564022,"alleles":["C","G","T"]},{"source":"dbSNP","start":140564024,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140564024,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797737043"},{"seq_region_name":"7","id":"rs1797737158","clinical_significance":[],"start":140564031,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140564031,"strand":1,"feature_type":"variation"},{"alleles":["G","C"],"end":140564035,"feature_type":"variation","strand":1,"source":"dbSNP","start":140564035,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797737263"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797737370","source":"dbSNP","start":140564043,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140564043,"alleles":["G","T"],"feature_type":"variation","strand":1},{"alleles":["G","A"],"end":140564045,"strand":1,"feature_type":"variation","start":140564045,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1427143485","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797737566","feature_type":"variation","strand":1,"end":140564046,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564046},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564052,"source":"dbSNP","strand":1,"feature_type":"variation","end":140564052,"alleles":["G","A"],"seq_region_name":"7","id":"rs1585642201","clinical_significance":[]},{"end":140564054,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140564054,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1383715206"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140564057,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564057,"clinical_significance":[],"id":"rs1004153848","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140564058,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564058,"source":"dbSNP","seq_region_name":"7","id":"rs1585642222","clinical_significance":[]},{"source":"dbSNP","start":140564062,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140564062,"alleles":["C","CC"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1312243181"},{"source":"dbSNP","start":140564066,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140564066,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs181051536","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1797738350","seq_region_name":"7","feature_type":"variation","strand":1,"end":140564069,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564069},{"end":140564072,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140564072,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs73165430","clinical_significance":[]},{"source":"dbSNP","start":140564085,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140564085,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797738562"},{"source":"dbSNP","start":140564097,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140564097,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1183327726"},{"clinical_significance":[],"seq_region_name":"7","id":"rs570894656","source":"dbSNP","start":140564100,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140564100,"alleles":["T","C"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564103,"feature_type":"variation","strand":1,"end":140564103,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs997536979"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797739007","source":"dbSNP","start":140564108,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140564108,"alleles":["C","T"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140564110,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140564110,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797739106"},{"alleles":["A","G"],"end":140564112,"feature_type":"variation","strand":1,"source":"dbSNP","start":140564112,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797739227"},{"seq_region_name":"7","id":"rs1249248532","clinical_significance":[],"strand":1,"feature_type":"variation","end":140564116,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564116,"source":"dbSNP"},{"start":140564117,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140564117,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs531829430","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797739714","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564125,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140564125},{"feature_type":"variation","strand":1,"end":140564127,"alleles":["A","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564127,"clinical_significance":[],"seq_region_name":"7","id":"rs1797739861"},{"clinical_significance":[],"id":"rs1797740024","seq_region_name":"7","source":"dbSNP","start":140564129,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140564133,"alleles":["AAAAA","AAAA"],"feature_type":"variation","strand":1},{"start":140564136,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140564136,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797740180","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797740322","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564137,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140564137},{"end":140564139,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140564139,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1047856474"},{"id":"rs1029370836","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140564142,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564142,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1238019289","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564150,"feature_type":"variation","strand":1,"end":140564150,"alleles":["G","C"]},{"seq_region_name":"7","id":"rs1797741035","clinical_significance":[],"strand":1,"feature_type":"variation","end":140564156,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564156,"source":"dbSNP"},{"end":140564157,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140564157,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797741213","clinical_significance":[]},{"alleles":["A","G"],"end":140564163,"strand":1,"feature_type":"variation","start":140564163,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585642323","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140564164,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564164,"clinical_significance":[],"seq_region_name":"7","id":"rs1797741562"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564165,"feature_type":"variation","strand":1,"end":140564165,"alleles":["C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1797741667"},{"seq_region_name":"7","id":"rs186467616","clinical_significance":[],"strand":1,"feature_type":"variation","end":140564167,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564167,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1245061637","clinical_significance":[],"end":140564170,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140564170,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1797742021","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140564172,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564172,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1186005486","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140564175,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564175,"source":"dbSNP"},{"start":140564176,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140564176,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs774572974","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1423340457","alleles":["G","A","T"],"end":140564177,"feature_type":"variation","strand":1,"source":"dbSNP","start":140564177,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1171345249","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564181,"feature_type":"variation","strand":1,"end":140564181,"alleles":["G","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797742699","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564186,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140564186},{"clinical_significance":[],"id":"rs1324303519","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564204,"feature_type":"variation","strand":1,"end":140564204,"alleles":["A","G"]},{"id":"rs1797742902","seq_region_name":"7","clinical_significance":[],"alleles":["C","A"],"end":140564206,"strand":1,"feature_type":"variation","start":140564206,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564207,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140564207,"clinical_significance":[],"seq_region_name":"7","id":"rs1375005293"},{"feature_type":"variation","strand":1,"end":140564208,"alleles":["G","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564208,"clinical_significance":[],"seq_region_name":"7","id":"rs568097911"},{"end":140564211,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140564211,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1040081444"},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140564212,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564212,"source":"dbSNP","seq_region_name":"7","id":"rs1460225921","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs967516261","end":140564216,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140564216,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140564217,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140564217,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1797743590","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130584615","end":140564220,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140564220,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140564222,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140564222,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs668402","clinical_significance":[]},{"source":"dbSNP","start":140564226,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140564226,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1408229661","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1159899859","source":"dbSNP","start":140564229,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140564229,"alleles":["G","A"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140564230,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564230,"clinical_significance":[],"seq_region_name":"7","id":"rs1468303141"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797744205","end":140564234,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140564234,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140564236,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140564236,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs149915605"},{"end":140564238,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140564238,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1199516020","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1797744431","seq_region_name":"7","source":"dbSNP","start":140564239,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140564239,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797744532","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564241,"feature_type":"variation","strand":1,"end":140564241,"alleles":["C","A"]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140564244,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564244,"source":"dbSNP","seq_region_name":"7","id":"rs1481375195","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564248,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G","T"],"end":140564248,"seq_region_name":"7","id":"rs528768","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797745004","clinical_significance":[],"strand":1,"feature_type":"variation","end":140564251,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564251,"source":"dbSNP"},{"source":"dbSNP","start":140564252,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140564252,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1221431625"},{"clinical_significance":[],"id":"rs668466","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","A","C","G"],"end":140564256,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564256},{"seq_region_name":"7","id":"rs1797745422","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564262,"source":"dbSNP","strand":1,"feature_type":"variation","end":140564262,"alleles":["A","C"]},{"end":140564263,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140564263,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs999422648"},{"end":140564266,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140564266,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1350243253","seq_region_name":"7"},{"id":"rs1797745738","seq_region_name":"7","clinical_significance":[],"end":140564267,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140564267,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1283928288","clinical_significance":[],"alleles":["G","C"],"end":140564272,"strand":1,"feature_type":"variation","start":140564272,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140564275,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140564275,"strand":1,"feature_type":"variation","id":"rs1675850951","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564277,"feature_type":"variation","strand":1,"end":140564277,"alleles":["T","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1797745938"},{"feature_type":"variation","strand":1,"end":140564279,"alleles":["T","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564279,"clinical_significance":[],"seq_region_name":"7","id":"rs1225497435"},{"id":"rs1563144125","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564279,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TCA","-"],"end":140564281},{"clinical_significance":[],"id":"rs1344152947","seq_region_name":"7","source":"dbSNP","start":140564280,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","-"],"end":140564280,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564280,"feature_type":"variation","strand":1,"end":140564280,"alleles":["C","A","G"],"clinical_significance":[],"id":"rs1459918312","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564280,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CA","-"],"end":140564281,"seq_region_name":"7","id":"rs1491289553","clinical_significance":[]},{"source":"dbSNP","start":140564280,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140564282,"alleles":["CAA","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1214654539"},{"seq_region_name":"7","id":"rs142073371","clinical_significance":[],"start":140564281,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140564297,"alleles":["AAAAAAAAAAAAAAAAA","AAAAAAAAAA","AAAAAAAAAAAA","AAAAAAAAAAAAA","AAAAAAAAAAAAAA","AAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAA"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564287,"feature_type":"variation","strand":1,"end":140564287,"alleles":["A","C"],"clinical_significance":[],"id":"rs1031439937","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140564292,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564292,"source":"dbSNP","id":"rs1797747295","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1297206552","clinical_significance":[],"strand":1,"feature_type":"variation","end":140564292,"alleles":["-","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564293,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140564293,"alleles":["A","ATA","ATACA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564293,"clinical_significance":[],"seq_region_name":"7","id":"rs1554469297"},{"id":"rs1305393009","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564294,"source":"dbSNP","strand":1,"feature_type":"variation","end":140564293,"alleles":["-","T"]},{"feature_type":"variation","strand":1,"end":140564294,"alleles":["A","C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564294,"clinical_significance":[],"seq_region_name":"7","id":"rs1205612647"},{"end":140564299,"alleles":["AAAATA","A"],"strand":1,"feature_type":"variation","start":140564294,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1797747852","seq_region_name":"7","clinical_significance":[]},{"alleles":["AAAATACA","A"],"end":140564301,"feature_type":"variation","strand":1,"source":"dbSNP","start":140564294,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1198548015"},{"clinical_significance":[],"seq_region_name":"7","id":"rs60977409","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564295,"feature_type":"variation","strand":1,"end":140564294,"alleles":["-","C","CAC","T","TAC","TACAC","TACACAC","TACACACAC"]},{"id":"rs1554469307","seq_region_name":"7","clinical_significance":[],"start":140564295,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140564295,"alleles":["A","ATA","ATACA"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564295,"feature_type":"variation","strand":1,"end":140564295,"alleles":["A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1563144169"},{"seq_region_name":"7","id":"rs1563144176","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["AAAT","TACACAC"],"end":140564298,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564295,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140564299,"alleles":["AAATA","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564295,"source":"dbSNP","seq_region_name":"7","id":"rs1563144182","clinical_significance":[]},{"clinical_significance":[],"id":"rs56667133","seq_region_name":"7","end":140564295,"alleles":["-","C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140564296,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs200775215","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140564296,"alleles":["A","C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564296,"source":"dbSNP"},{"seq_region_name":"7","id":"rs11407278","clinical_significance":[],"start":140564297,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["-","C","CAC","CACAC","T","TACAC"],"end":140564296,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1554469312","source":"dbSNP","start":140564297,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","AATA","ACA","ACACA"],"end":140564297,"feature_type":"variation","strand":1},{"alleles":["T","A","C"],"end":140564298,"feature_type":"variation","strand":1,"source":"dbSNP","start":140564298,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs60901407"},{"clinical_significance":[],"seq_region_name":"7","id":"rs200254428","end":140564298,"alleles":["T","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140564298,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1554469316","clinical_significance":[],"start":140564299,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","AA"],"end":140564299,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs375771552","feature_type":"variation","strand":1,"alleles":["ACACACACACACACA","ACACACACACA","ACACACACACACA","ACACACACACACACACA","ACACACACACACACACACA","ACACACACACACACACACACA","ACACACACACACACACACACACA"],"end":140564313,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564299},{"id":"rs1165922783","seq_region_name":"7","clinical_significance":[],"start":140564300,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140564300,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs915532118","clinical_significance":[],"start":140564302,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140564302,"alleles":["C","A","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1797751156","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564305,"source":"dbSNP","strand":1,"feature_type":"variation","end":140564309,"alleles":["ACACA","ACACATACACA"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564306,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140564306,"id":"rs1797751315","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797751480","clinical_significance":[],"strand":1,"feature_type":"variation","end":140564307,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564307,"source":"dbSNP"},{"source":"dbSNP","start":140564312,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140564312,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1243564656","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1797751792","clinical_significance":[],"strand":1,"feature_type":"variation","end":140564313,"alleles":["A","ACACAAA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564313,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564315,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140564315,"seq_region_name":"7","id":"rs1797751894","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["ACACT","ACACTACACT"],"end":140564321,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564317,"clinical_significance":[],"seq_region_name":"7","id":"rs1462080735"},{"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140564327,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564327,"source":"dbSNP","id":"rs78051654","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","A","C","G"],"end":140564332,"feature_type":"variation","strand":1,"source":"dbSNP","start":140564332,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs916660250"},{"start":140564333,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140564333,"alleles":["A","T"],"strand":1,"feature_type":"variation","id":"rs1271563973","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1048152037","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564335,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140564335},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564336,"source":"dbSNP","strand":1,"feature_type":"variation","end":140564338,"alleles":["TTT","TT"],"id":"rs969584393","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140564340,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564340,"source":"dbSNP","id":"rs2130585266","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797752773","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140564351,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564351},{"source":"dbSNP","start":140564352,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140564352,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1482928292"},{"seq_region_name":"7","id":"rs1797752981","clinical_significance":[],"alleles":["G","A"],"end":140564356,"strand":1,"feature_type":"variation","start":140564356,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["C","T"],"end":140564360,"feature_type":"variation","strand":1,"source":"dbSNP","start":140564360,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1454194132","seq_region_name":"7"},{"clinical_significance":[],"id":"rs145999398","seq_region_name":"7","source":"dbSNP","start":140564362,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140564362,"feature_type":"variation","strand":1},{"id":"rs556212795","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140564364,"strand":1,"feature_type":"variation","start":140564364,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1040868165","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140564366,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564366,"source":"dbSNP"},{"start":140564372,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140564372,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1476946165","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130585338","end":140564375,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140564375,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564378,"source":"dbSNP","strand":1,"feature_type":"variation","end":140564378,"alleles":["G","C"],"seq_region_name":"7","id":"rs1797753617","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797753703","source":"dbSNP","start":140564384,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140564384,"alleles":["C","T"],"feature_type":"variation","strand":1},{"id":"rs574459152","seq_region_name":"7","clinical_significance":[],"start":140564385,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140564385,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs540100735","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140564392,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564392},{"end":140564395,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140564395,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797754056"},{"end":140564396,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140564396,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1429058115","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140564398,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564398,"source":"dbSNP","seq_region_name":"7","id":"rs1797754254","clinical_significance":[]},{"source":"dbSNP","start":140564399,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140564399,"alleles":["A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797754358"},{"seq_region_name":"7","id":"rs1170294884","clinical_significance":[],"start":140564400,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140564400,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1165247298","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564402,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140564402},{"start":140564403,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140564403,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797754662","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564404,"source":"dbSNP","strand":1,"feature_type":"variation","end":140564404,"alleles":["A","G"],"seq_region_name":"7","id":"rs1050464025","clinical_significance":[]},{"seq_region_name":"7","id":"rs1443009115","clinical_significance":[],"start":140564410,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140564410,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1797754954","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140564417,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564417,"source":"dbSNP"},{"id":"rs1384911320","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564418,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C","T"],"end":140564418},{"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140564419,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564419,"source":"dbSNP","seq_region_name":"7","id":"rs1429670773","clinical_significance":[]},{"alleles":["A","C"],"end":140564426,"feature_type":"variation","strand":1,"source":"dbSNP","start":140564426,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1231284460"},{"end":140564427,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140564427,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1470850406","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797755405","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140564429,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564429,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1797755517","clinical_significance":[],"end":140564440,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140564440,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140564444,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140564444,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1490659838","clinical_significance":[]},{"id":"rs764223747","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564445,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140564445},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797755833","alleles":["ATAAATAA","ATAA"],"end":140564455,"feature_type":"variation","strand":1,"source":"dbSNP","start":140564448,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140564455,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564455,"clinical_significance":[],"id":"rs1173782464","seq_region_name":"7"},{"start":140564457,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140564457,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1356802196","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140564461,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564461,"source":"dbSNP","seq_region_name":"7","id":"rs1311626824","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797756241","clinical_significance":[],"end":140564466,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140564466,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs530660","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140564467,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564467,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564470,"feature_type":"variation","strand":1,"end":140564470,"alleles":["A","G"],"clinical_significance":[],"id":"rs1374818850","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564471,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140564471,"clinical_significance":[],"seq_region_name":"7","id":"rs1021655659"},{"id":"rs1295961784","seq_region_name":"7","clinical_significance":[],"end":140564472,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140564472,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564476,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140564476,"seq_region_name":"7","id":"rs1797756860","clinical_significance":[]},{"end":140564479,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140564479,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1047286390"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140564480,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564480,"source":"dbSNP","id":"rs768348019","seq_region_name":"7","clinical_significance":[]},{"end":140564486,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140564486,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs368558691"},{"clinical_significance":[],"id":"rs998980777","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564487,"feature_type":"variation","strand":1,"end":140564487,"alleles":["G","A"]},{"clinical_significance":[],"id":"rs1422569103","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564488,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140564488},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564492,"source":"dbSNP","strand":1,"feature_type":"variation","end":140564496,"alleles":["AAAAA","AAAAAA"],"seq_region_name":"7","id":"rs1349483917","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797757494","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140564496,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564496},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140564506,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564506,"clinical_significance":[],"seq_region_name":"7","id":"rs1160052521"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564516,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140564516,"seq_region_name":"7","id":"rs2130585643","clinical_significance":[]},{"source":"dbSNP","start":140564520,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140564520,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1421130042"},{"start":140564522,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140564522,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1040131115","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1036242978","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564525,"feature_type":"variation","strand":1,"end":140564525,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs669797","alleles":["C","A","T"],"end":140564529,"feature_type":"variation","strand":1,"source":"dbSNP","start":140564529,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140564530,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G","T"],"end":140564530,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1481046111"},{"seq_region_name":"7","id":"rs191319662","clinical_significance":[],"alleles":["A","G"],"end":140564535,"strand":1,"feature_type":"variation","start":140564535,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140564538,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140564538,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs931692585"},{"id":"rs1220685738","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564539,"source":"dbSNP","strand":1,"feature_type":"variation","end":140564539,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1797758670","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564542,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140564542},{"feature_type":"variation","strand":1,"end":140564543,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564543,"clinical_significance":[],"id":"rs1797758779","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564544,"source":"dbSNP","strand":1,"feature_type":"variation","end":140564544,"alleles":["A","C"],"seq_region_name":"7","id":"rs1797758878","clinical_significance":[]},{"source":"dbSNP","start":140564547,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140564547,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1043965666","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140564549,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564549,"source":"dbSNP","seq_region_name":"7","id":"rs1797759087","clinical_significance":[]},{"seq_region_name":"7","id":"rs1261707174","clinical_significance":[],"alleles":["G","A"],"end":140564555,"strand":1,"feature_type":"variation","start":140564555,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["AAAAGAAAA","AAAAGAAAAGAAAA"],"end":140564565,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564557,"source":"dbSNP","id":"rs1797759284","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564561,"feature_type":"variation","strand":1,"end":140564561,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1797759403"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140564571,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564571,"clinical_significance":[],"seq_region_name":"7","id":"rs992137341"},{"clinical_significance":[],"seq_region_name":"7","id":"rs915600713","feature_type":"variation","strand":1,"end":140564572,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564572},{"clinical_significance":[],"seq_region_name":"7","id":"rs952352503","feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140564574,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564574},{"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140564575,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564575,"clinical_significance":[],"seq_region_name":"7","id":"rs1227309487"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564578,"source":"dbSNP","strand":1,"feature_type":"variation","end":140564578,"alleles":["C","T"],"id":"rs527570224","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140564579,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564579,"source":"dbSNP","seq_region_name":"7","id":"rs780106693","clinical_significance":[]},{"seq_region_name":"7","id":"rs896522751","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564592,"source":"dbSNP","strand":1,"feature_type":"variation","end":140564592,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs939714617","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564595,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140564595},{"clinical_significance":[],"seq_region_name":"7","id":"rs781765381","source":"dbSNP","start":140564597,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TT","T"],"end":140564598,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1403060798","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564599,"source":"dbSNP","strand":1,"feature_type":"variation","end":140564599,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1389687673","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140564601,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564601},{"strand":1,"feature_type":"variation","end":140564610,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564610,"source":"dbSNP","id":"rs1040904082","seq_region_name":"7","clinical_significance":[]},{"id":"rs922399925","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140564612,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564612,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1343720693","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140564615,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564615},{"seq_region_name":"7","id":"rs1797760950","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564617,"source":"dbSNP","strand":1,"feature_type":"variation","end":140564617,"alleles":["A","C"]},{"end":140564619,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140564619,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1158501348","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1312111479","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564620,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140564620},{"strand":1,"feature_type":"variation","end":140564622,"alleles":["A","C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564622,"source":"dbSNP","seq_region_name":"7","id":"rs1217216076","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797761475","alleles":["T","G"],"end":140564624,"feature_type":"variation","strand":1,"source":"dbSNP","start":140564624,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564628,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140564628,"clinical_significance":[],"id":"rs1797761562","seq_region_name":"7"},{"seq_region_name":"7","id":"rs969470255","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564630,"source":"dbSNP","strand":1,"feature_type":"variation","end":140564630,"alleles":["A","G","T"]},{"seq_region_name":"7","id":"rs1262790649","clinical_significance":[],"alleles":["C","T"],"end":140564632,"strand":1,"feature_type":"variation","start":140564632,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797761911","end":140564635,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140564635,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs932614875","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564642,"feature_type":"variation","strand":1,"end":140564642,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797762150","alleles":["A","G"],"end":140564646,"feature_type":"variation","strand":1,"source":"dbSNP","start":140564646,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140564651,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140564651,"alleles":["G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797762276","clinical_significance":[]},{"source":"dbSNP","start":140564654,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140564654,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1487361648"},{"id":"rs183576014","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140564655,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564655,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564656,"source":"dbSNP","strand":1,"feature_type":"variation","end":140564656,"alleles":["T","C"],"id":"rs1258641396","seq_region_name":"7","clinical_significance":[]},{"start":140564659,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140564659,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797762722","clinical_significance":[]},{"seq_region_name":"7","id":"rs545726800","clinical_significance":[],"strand":1,"feature_type":"variation","end":140564660,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564660,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1585643781","seq_region_name":"7","source":"dbSNP","start":140564661,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140564661,"alleles":["C","A","G"],"feature_type":"variation","strand":1},{"alleles":["T","C"],"end":140564664,"strand":1,"feature_type":"variation","start":140564664,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797763056","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797763213","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564665,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140564665},{"source":"dbSNP","start":140564672,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140564679,"alleles":["AAAAAAAA","AAAAAAA","AAAAAAAAA"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1193164914","seq_region_name":"7"},{"start":140564677,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140564677,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","id":"rs1269872470","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1264481481","clinical_significance":[],"end":140564679,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140564679,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140564686,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140564686,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs564283568","seq_region_name":"7"},{"alleles":["T","C"],"end":140564687,"strand":1,"feature_type":"variation","start":140564687,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797764271","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797764443","clinical_significance":[],"start":140564690,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140564690,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140564691,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140564691,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585643845"},{"alleles":["G","A"],"end":140564692,"feature_type":"variation","strand":1,"source":"dbSNP","start":140564692,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1189231301"},{"seq_region_name":"7","id":"rs1027584069","clinical_significance":[],"start":140564695,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140564695,"strand":1,"feature_type":"variation"},{"end":140564696,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140564696,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1383760332","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs139934770","source":"dbSNP","start":140564698,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140564698,"feature_type":"variation","strand":1},{"alleles":["G","A","T"],"end":140564704,"strand":1,"feature_type":"variation","start":140564704,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797765471","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564708,"feature_type":"variation","strand":1,"alleles":["C","-"],"end":140564708,"clinical_significance":[],"id":"rs1320186824","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1797765835","clinical_significance":[],"start":140564709,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AATAAT","AAT"],"end":140564714,"strand":1,"feature_type":"variation"},{"id":"rs1161270521","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["AA","A"],"end":140564713,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564712,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1453688083","clinical_significance":[],"alleles":["ATCATTTGATCATT","ATCATT"],"end":140564726,"strand":1,"feature_type":"variation","start":140564713,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797766205","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564714,"feature_type":"variation","strand":1,"end":140564714,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs947398482","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564716,"feature_type":"variation","strand":1,"end":140564716,"alleles":["A","T"]},{"seq_region_name":"7","id":"rs1408319189","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564717,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140564717},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564723,"source":"dbSNP","strand":1,"feature_type":"variation","end":140564723,"alleles":["C","T"],"id":"rs1358021505","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564725,"feature_type":"variation","strand":1,"end":140564725,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs983468228"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797767088","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140564731,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564731},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140564734,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564734,"source":"dbSNP","id":"rs1797767268","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140564735,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140564735,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1418599346"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564737,"feature_type":"variation","strand":1,"end":140564737,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs912803120"},{"seq_region_name":"7","id":"rs1172961659","clinical_significance":[],"end":140564738,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140564738,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797767897","end":140564741,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140564741,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1427152532","source":"dbSNP","start":140564743,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140564751,"alleles":["TAACTAACT","TAACT"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1042997493","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564744,"source":"dbSNP","strand":1,"feature_type":"variation","end":140564744,"alleles":["A","T"]},{"end":140564752,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140564752,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1797768376","seq_region_name":"7"},{"end":140564753,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140564753,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797768543","clinical_significance":[]},{"end":140564754,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140564754,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797768702","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797768876","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140564755,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564755,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797769027","end":140564758,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140564758,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1797769168","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564762,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140564762},{"alleles":["C","T"],"end":140564764,"strand":1,"feature_type":"variation","start":140564764,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130586361","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1247833856","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140564767,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564767},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797769508","source":"dbSNP","start":140564768,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140564768,"alleles":["C","T"],"feature_type":"variation","strand":1},{"id":"rs944413563","seq_region_name":"7","clinical_significance":[],"start":140564769,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140564769,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1797769865","clinical_significance":[],"start":140564776,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140564776,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564777,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140564777,"seq_region_name":"7","id":"rs1797770029","clinical_significance":[]},{"start":140564778,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140564778,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797770225","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564779,"feature_type":"variation","strand":1,"end":140564779,"alleles":["C","T"],"clinical_significance":[],"id":"rs2130586407","seq_region_name":"7"},{"start":140564781,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140564781,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1461499594","clinical_significance":[]},{"alleles":["C","T"],"end":140564782,"feature_type":"variation","strand":1,"source":"dbSNP","start":140564782,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs143468022"},{"clinical_significance":[],"seq_region_name":"7","id":"rs188259709","source":"dbSNP","start":140564785,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140564785,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1201302299","end":140564813,"alleles":["ATTAAGCATTGCCACGTGAACAGCATT","ATT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140564787,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["T","C"],"end":140564788,"strand":1,"feature_type":"variation","start":140564788,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797770849","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797771010","clinical_significance":[],"strand":1,"feature_type":"variation","end":140564793,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564793,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs921565913","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564797,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140564797},{"source":"dbSNP","start":140564798,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140564798,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1251863375"},{"alleles":["C","T"],"end":140564801,"feature_type":"variation","strand":1,"source":"dbSNP","start":140564801,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs754852159"},{"source":"dbSNP","start":140564802,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140564802,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs780678270"},{"id":"rs1797771888","seq_region_name":"7","clinical_significance":[],"alleles":["A","C"],"end":140564811,"strand":1,"feature_type":"variation","start":140564811,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797772051","source":"dbSNP","start":140564812,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140564812,"alleles":["T","C"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140564814,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564814,"clinical_significance":[],"seq_region_name":"7","id":"rs1797772231"},{"feature_type":"variation","strand":1,"end":140564814,"alleles":["G","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564814,"clinical_significance":[],"seq_region_name":"7","id":"rs1797772374"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797772470","alleles":["G","A"],"end":140564816,"feature_type":"variation","strand":1,"source":"dbSNP","start":140564816,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs2130586543","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564822,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140564822},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564823,"source":"dbSNP","strand":1,"feature_type":"variation","end":140564823,"alleles":["C","G"],"seq_region_name":"7","id":"rs1797772582","clinical_significance":[]},{"id":"rs1797772681","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564824,"source":"dbSNP","strand":1,"feature_type":"variation","end":140564824,"alleles":["C","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797772787","feature_type":"variation","strand":1,"end":140564827,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564827},{"id":"rs1296619730","seq_region_name":"7","clinical_significance":[],"start":140564830,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140564830,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564833,"source":"dbSNP","strand":1,"feature_type":"variation","end":140564833,"alleles":["T","C"],"id":"rs1797772990","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1035889534","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140564834,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564834,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140564835,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564835,"clinical_significance":[],"seq_region_name":"7","id":"rs573671168"},{"end":140564837,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140564837,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797773607"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797773752","source":"dbSNP","start":140564838,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140564838,"alleles":["A","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797773922","feature_type":"variation","strand":1,"end":140564842,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564842},{"clinical_significance":[],"seq_region_name":"7","id":"rs1043466368","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564845,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140564845},{"feature_type":"variation","strand":1,"end":140564852,"alleles":["CAGGACAG","CAG"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564845,"clinical_significance":[],"seq_region_name":"7","id":"rs1797774234"},{"strand":1,"feature_type":"variation","end":140564847,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564847,"source":"dbSNP","seq_region_name":"7","id":"rs1334772863","clinical_significance":[]},{"seq_region_name":"7","id":"rs903715448","clinical_significance":[],"start":140564848,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140564848,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1797774551","seq_region_name":"7","alleles":["A","T"],"end":140564849,"feature_type":"variation","strand":1,"source":"dbSNP","start":140564849,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1797774720","seq_region_name":"7","feature_type":"variation","strand":1,"end":140564851,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564851},{"clinical_significance":[],"id":"rs1585644195","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564853,"feature_type":"variation","strand":1,"end":140564853,"alleles":["C","A"]},{"seq_region_name":"7","id":"rs1397800387","clinical_significance":[],"alleles":["C","A","T"],"end":140564854,"strand":1,"feature_type":"variation","start":140564854,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140564858,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564858,"clinical_significance":[],"seq_region_name":"7","id":"rs1797775056"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564860,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140564860,"clinical_significance":[],"id":"rs747748960","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1224778509","alleles":["G","A"],"end":140564861,"feature_type":"variation","strand":1,"source":"dbSNP","start":140564861,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1797775602","seq_region_name":"7","clinical_significance":[],"end":140564862,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140564862,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797775757","alleles":["CA","-"],"end":140564866,"feature_type":"variation","strand":1,"source":"dbSNP","start":140564865,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1797775916","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564871,"feature_type":"variation","strand":1,"alleles":["TCTCT","TCT"],"end":140564875},{"end":140564875,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","start":140564875,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs935173547","clinical_significance":[]},{"source":"dbSNP","start":140564878,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140564878,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1585644241","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1389875413","alleles":["G","A"],"end":140564879,"feature_type":"variation","strand":1,"source":"dbSNP","start":140564879,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797776571","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564881,"feature_type":"variation","strand":1,"end":140564881,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1013204994","source":"dbSNP","start":140564888,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140564888,"feature_type":"variation","strand":1},{"id":"rs1797776916","seq_region_name":"7","clinical_significance":[],"start":140564892,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140564892,"strand":1,"feature_type":"variation"},{"end":140564895,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140564895,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1023633035","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564896,"feature_type":"variation","strand":1,"end":140564896,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1286992258"},{"seq_region_name":"7","id":"rs1052820477","clinical_significance":[],"end":140564898,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140564898,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140564901,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140564901,"alleles":["A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1216000047"},{"source":"dbSNP","start":140564901,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AG","-"],"end":140564902,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1797777549","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140564903,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564903,"clinical_significance":[],"seq_region_name":"7","id":"rs555516"},{"end":140564904,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140564904,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1441374375","clinical_significance":[]},{"id":"rs1250650988","seq_region_name":"7","clinical_significance":[],"start":140564907,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140564907,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1585644333","seq_region_name":"7","feature_type":"variation","strand":1,"end":140564909,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564909},{"alleles":["T","C"],"end":140564913,"strand":1,"feature_type":"variation","start":140564913,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1197428797","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs2130586841","seq_region_name":"7","end":140564914,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140564914,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140564915,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564915,"clinical_significance":[],"seq_region_name":"7","id":"rs983792400"},{"end":140564919,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140564919,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1013475510"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564920,"feature_type":"variation","strand":1,"end":140564920,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1246520514"},{"end":140564922,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140564922,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs547378818"},{"seq_region_name":"7","id":"rs1797779057","clinical_significance":[],"start":140564927,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140564927,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564930,"feature_type":"variation","strand":1,"end":140564930,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1023655148"},{"feature_type":"variation","strand":1,"end":140564931,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564931,"clinical_significance":[],"seq_region_name":"7","id":"rs566292156"},{"alleles":["GG","G"],"end":140564932,"strand":1,"feature_type":"variation","start":140564931,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1313240165","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564934,"source":"dbSNP","strand":1,"feature_type":"variation","end":140564942,"alleles":["AAAAAAAAA","AAAAAAAA","AAAAAAAAAA"],"seq_region_name":"7","id":"rs1309255190","clinical_significance":[]},{"source":"dbSNP","start":140564935,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140564935,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs540106504"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564952,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140564952,"clinical_significance":[],"seq_region_name":"7","id":"rs1585644414"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564953,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140564953,"clinical_significance":[],"seq_region_name":"7","id":"rs1585644428"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797780413","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564954,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140564954},{"end":140564955,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140564955,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130586948"},{"feature_type":"variation","strand":1,"end":140564962,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564962,"clinical_significance":[],"id":"rs1563144673","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797780741","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564964,"feature_type":"variation","strand":1,"end":140564964,"alleles":["G","A"]},{"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140564965,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564965,"source":"dbSNP","seq_region_name":"7","id":"rs1245894552","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs748861571","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564966,"feature_type":"variation","strand":1,"end":140564966,"alleles":["G","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797781321","feature_type":"variation","strand":1,"end":140564974,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564974},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130587001","source":"dbSNP","start":140564976,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140564976,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585644457","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564979,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140564979},{"id":"rs1426997877","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140564987,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564987,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797781836","source":"dbSNP","start":140564989,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140564989,"alleles":["A","C"],"feature_type":"variation","strand":1},{"end":140564990,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140564990,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1178842002","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140564993,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564993,"source":"dbSNP","seq_region_name":"7","id":"rs1797782190","clinical_significance":[]},{"id":"rs922485213","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140564997,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140564997},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140564999,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140564999,"clinical_significance":[],"seq_region_name":"7","id":"rs1797782548"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565002,"source":"dbSNP","strand":1,"feature_type":"variation","end":140565002,"alleles":["A","G"],"seq_region_name":"7","id":"rs2130587064","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1438483505","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565006,"feature_type":"variation","strand":1,"end":140565006,"alleles":["G","A"]},{"id":"rs1797782719","seq_region_name":"7","clinical_significance":[],"start":140565009,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140565009,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1363806579","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140565010,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565010},{"strand":1,"feature_type":"variation","alleles":["GTGAGTG","GTG"],"end":140565016,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565010,"source":"dbSNP","id":"rs1472272422","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565011,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140565011,"clinical_significance":[],"seq_region_name":"7","id":"rs1585644503"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565016,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140565016,"seq_region_name":"7","id":"rs573380102","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797783526","source":"dbSNP","start":140565017,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140565017,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140565020,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565020,"source":"dbSNP","seq_region_name":"7","id":"rs1471564396","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565021,"feature_type":"variation","strand":1,"end":140565021,"alleles":["C","T"],"clinical_significance":[],"id":"rs1797783858","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140565030,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565030,"clinical_significance":[],"seq_region_name":"7","id":"rs1366971998"},{"strand":1,"feature_type":"variation","end":140565031,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565031,"source":"dbSNP","seq_region_name":"7","id":"rs1222911633","clinical_significance":[]},{"end":140565032,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140565032,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs985277616","clinical_significance":[]},{"id":"rs79148594","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140565033,"strand":1,"feature_type":"variation","start":140565033,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1797784719","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565040,"source":"dbSNP","strand":1,"feature_type":"variation","end":140565040,"alleles":["A","G"]},{"feature_type":"variation","strand":1,"end":140565041,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565041,"clinical_significance":[],"seq_region_name":"7","id":"rs1209402821"},{"source":"dbSNP","start":140565051,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140565051,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797785045"},{"clinical_significance":[],"seq_region_name":"7","id":"rs570199277","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565053,"feature_type":"variation","strand":1,"end":140565053,"alleles":["A","G"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565054,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140565054,"seq_region_name":"7","id":"rs771873646","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140565055,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565055,"clinical_significance":[],"seq_region_name":"7","id":"rs1797785578"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1349620743","source":"dbSNP","start":140565058,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140565058,"alleles":["C","T"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565059,"source":"dbSNP","strand":1,"feature_type":"variation","end":140565059,"alleles":["A","G"],"seq_region_name":"7","id":"rs982966159","clinical_significance":[]},{"alleles":["T","A"],"end":140565060,"strand":1,"feature_type":"variation","start":140565060,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1019699689","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797786293","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565065,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140565065},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585644642","alleles":["C","T"],"end":140565066,"feature_type":"variation","strand":1,"source":"dbSNP","start":140565066,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["T","C"],"end":140565067,"strand":1,"feature_type":"variation","start":140565067,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs946612399","clinical_significance":[]},{"alleles":["T","C"],"end":140565069,"strand":1,"feature_type":"variation","start":140565069,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1407329172","clinical_significance":[]},{"seq_region_name":"7","id":"rs1343969388","clinical_significance":[],"strand":1,"feature_type":"variation","end":140565073,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565073,"source":"dbSNP"},{"start":140565076,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140565076,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs868534039","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565089,"feature_type":"variation","strand":1,"end":140565089,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1797787298"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797787458","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140565092,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565092},{"clinical_significance":[],"id":"rs1585644692","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565093,"feature_type":"variation","strand":1,"end":140565093,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1043051032","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565095,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140565095},{"clinical_significance":[],"seq_region_name":"7","id":"rs537963756","alleles":["T","A"],"end":140565103,"feature_type":"variation","strand":1,"source":"dbSNP","start":140565103,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140565106,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140565106,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797787890","clinical_significance":[]},{"seq_region_name":"7","id":"rs556245066","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140565112,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565112,"source":"dbSNP"},{"start":140565113,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140565113,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797788235","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565115,"feature_type":"variation","strand":1,"end":140565115,"alleles":["G","T"],"clinical_significance":[],"id":"rs975615004","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565119,"source":"dbSNP","strand":1,"feature_type":"variation","end":140565119,"alleles":["A","G"],"id":"rs1797788552","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1057461604","clinical_significance":[],"end":140565132,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140565132,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140565143,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565143,"clinical_significance":[],"seq_region_name":"7","id":"rs2130587342"},{"clinical_significance":[],"seq_region_name":"7","id":"rs896016995","source":"dbSNP","start":140565148,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140565148,"alleles":["G","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1013512618","alleles":["A","G"],"end":140565149,"feature_type":"variation","strand":1,"source":"dbSNP","start":140565149,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1023096722","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565151,"source":"dbSNP","strand":1,"feature_type":"variation","end":140565151,"alleles":["G","A","C"]},{"alleles":["G","C"],"end":140565155,"feature_type":"variation","strand":1,"source":"dbSNP","start":140565155,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs544188206"},{"clinical_significance":[],"id":"rs1410626828","seq_region_name":"7","end":140565156,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140565156,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1797790092","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140565157,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565157,"source":"dbSNP"},{"end":140565158,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140565158,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797790282","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140565162,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565162,"source":"dbSNP","seq_region_name":"7","id":"rs1200002516","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140565163,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565163,"source":"dbSNP","seq_region_name":"7","id":"rs1797790608","clinical_significance":[]},{"id":"rs1797790760","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140565164,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565164,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565166,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140565166,"seq_region_name":"7","id":"rs1240140307","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565171,"feature_type":"variation","strand":1,"end":140565171,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1481385930"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565172,"feature_type":"variation","strand":1,"end":140565172,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130587457"},{"feature_type":"variation","strand":1,"end":140565173,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565173,"clinical_significance":[],"seq_region_name":"7","id":"rs1797791104"},{"clinical_significance":[],"seq_region_name":"7","id":"rs931638692","end":140565175,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140565175,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140565177,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140565177,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1197985669"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565180,"feature_type":"variation","strand":1,"end":140565180,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1005779511"},{"strand":1,"feature_type":"variation","end":140565186,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565186,"source":"dbSNP","seq_region_name":"7","id":"rs1797791689","clinical_significance":[]},{"seq_region_name":"7","id":"rs1286671797","clinical_significance":[],"start":140565191,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140565191,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140565192,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140565192,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs979628568"},{"id":"rs1361747992","seq_region_name":"7","clinical_significance":[],"start":140565193,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["GGGG","GGG"],"end":140565196,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1263855061","clinical_significance":[],"start":140565194,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140565194,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140565200,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140565200,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs925054874","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565201,"feature_type":"variation","strand":1,"end":140565201,"alleles":["G","A"],"clinical_significance":[],"id":"rs1797792395","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797792489","source":"dbSNP","start":140565202,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140565203,"alleles":["CC","CCC"],"feature_type":"variation","strand":1},{"start":140565214,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140565214,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1015298423","clinical_significance":[]},{"start":140565215,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140565215,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs935035987","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797792857","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140565217,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565217},{"clinical_significance":[],"seq_region_name":"7","id":"rs1343578559","feature_type":"variation","strand":1,"end":140565221,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565221},{"strand":1,"feature_type":"variation","end":140565231,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565231,"source":"dbSNP","id":"rs2130587603","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1052284297","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140565237,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565237,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1226777177","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565238,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140565238},{"id":"rs1289473749","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565239,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140565239},{"clinical_significance":[],"seq_region_name":"7","id":"rs535480928","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140565241,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565241},{"id":"rs73491591","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140565242,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565242,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1797793717","seq_region_name":"7","source":"dbSNP","start":140565244,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140565244,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1797793821","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565245,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140565245},{"feature_type":"variation","strand":1,"end":140565250,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565250,"clinical_significance":[],"seq_region_name":"7","id":"rs1206380768"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797794089","feature_type":"variation","strand":1,"end":140565254,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565254},{"seq_region_name":"7","id":"rs1236201047","clinical_significance":[],"alleles":["T","A"],"end":140565255,"strand":1,"feature_type":"variation","start":140565255,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1457260264","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565259,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140565259},{"clinical_significance":[],"id":"rs1797794414","seq_region_name":"7","source":"dbSNP","start":140565266,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140565266,"feature_type":"variation","strand":1},{"alleles":["C","T"],"end":140565270,"feature_type":"variation","strand":1,"source":"dbSNP","start":140565270,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs976567750"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1387207085","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140565279,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565279},{"seq_region_name":"7","id":"rs1176524592","clinical_significance":[],"strand":1,"feature_type":"variation","end":140565281,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565281,"source":"dbSNP"},{"source":"dbSNP","start":140565293,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140565293,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1029833889"},{"id":"rs1797794913","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140565294,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565294,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140565297,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565297,"clinical_significance":[],"id":"rs533097041","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565298,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140565298,"seq_region_name":"7","id":"rs1423045231","clinical_significance":[]},{"seq_region_name":"7","id":"rs1563144882","clinical_significance":[],"start":140565300,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140565300,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140565303,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565303,"clinical_significance":[],"id":"rs1797795186","seq_region_name":"7"},{"id":"rs1797795285","seq_region_name":"7","clinical_significance":[],"end":140565305,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140565305,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1171755962","seq_region_name":"7","source":"dbSNP","start":140565306,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140565306,"alleles":["A","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1475639702","clinical_significance":[],"start":140565307,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140565307,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"id":"rs2130587790","seq_region_name":"7","clinical_significance":[],"start":140565310,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140565310,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565319,"source":"dbSNP","strand":1,"feature_type":"variation","end":140565319,"alleles":["T","C"],"seq_region_name":"7","id":"rs374437437","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140565324,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565324,"clinical_significance":[],"id":"rs1797795710","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1186854693","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140565327,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565327},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130587835","alleles":["T","G"],"end":140565329,"feature_type":"variation","strand":1,"source":"dbSNP","start":140565329,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1797795937","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565330,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140565330},{"end":140565332,"alleles":["T","A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140565332,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797796047"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565333,"feature_type":"variation","strand":1,"end":140565333,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1464623569"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565334,"feature_type":"variation","strand":1,"end":140565334,"alleles":["G","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1243822020"},{"clinical_significance":[],"seq_region_name":"7","id":"rs868357558","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565336,"feature_type":"variation","strand":1,"end":140565336,"alleles":["G","A","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565337,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140565337,"clinical_significance":[],"id":"rs375884100","seq_region_name":"7"},{"seq_region_name":"7","id":"rs2130587892","clinical_significance":[],"strand":1,"feature_type":"variation","end":140565338,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565338,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1215703108","clinical_significance":[],"start":140565339,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C","T"],"end":140565339,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1278592751","clinical_significance":[],"strand":1,"feature_type":"variation","end":140565344,"alleles":["GGGGGG","GGGGG"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565339,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140565342,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565342,"source":"dbSNP","seq_region_name":"7","id":"rs1419803080","clinical_significance":[]},{"clinical_significance":[],"id":"rs1797797062","seq_region_name":"7","feature_type":"variation","strand":1,"end":140565343,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565343},{"alleles":["G","A"],"end":140565344,"feature_type":"variation","strand":1,"source":"dbSNP","start":140565344,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs576157493","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130587936","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565348,"feature_type":"variation","strand":1,"end":140565348,"alleles":["T","G"]},{"end":140565349,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140565349,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs977958974"},{"end":140565353,"alleles":["A","C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140565353,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs73491595"},{"start":140565359,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140565359,"strand":1,"feature_type":"variation","id":"rs1364094613","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140565362,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140565362,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797797551"},{"alleles":["T","C"],"end":140565364,"feature_type":"variation","strand":1,"source":"dbSNP","start":140565364,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1336801718"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565365,"source":"dbSNP","strand":1,"feature_type":"variation","end":140565364,"alleles":["-","TG"],"seq_region_name":"7","id":"rs1797797763","clinical_significance":[]},{"id":"rs1563144929","seq_region_name":"7","clinical_significance":[],"start":140565366,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140565366,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565367,"source":"dbSNP","strand":1,"feature_type":"variation","end":140565367,"alleles":["T","C"],"seq_region_name":"7","id":"rs1449644215","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797798088","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565368,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140565368},{"source":"dbSNP","start":140565368,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["GGG","G"],"end":140565370,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1357326910"},{"seq_region_name":"7","id":"rs560179552","clinical_significance":[],"start":140565374,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140565374,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565375,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140565375,"clinical_significance":[],"seq_region_name":"7","id":"rs1797798441"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1004669982","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565386,"feature_type":"variation","strand":1,"end":140565386,"alleles":["T","C"]},{"clinical_significance":[],"id":"rs1421310808","seq_region_name":"7","alleles":["A","G"],"end":140565393,"feature_type":"variation","strand":1,"source":"dbSNP","start":140565393,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140565394,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140565394,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1166486533","clinical_significance":[]},{"end":140565396,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140565396,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797798867","clinical_significance":[]},{"seq_region_name":"7","id":"rs1019752147","clinical_significance":[],"strand":1,"feature_type":"variation","end":140565397,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565397,"source":"dbSNP"},{"start":140565403,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140565403,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs684246","clinical_significance":[]},{"alleles":["G","A"],"end":140565407,"feature_type":"variation","strand":1,"source":"dbSNP","start":140565407,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs766026952"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565409,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140565409,"id":"rs1797799427","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140565413,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140565413,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1797799550","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140565416,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565416,"clinical_significance":[],"seq_region_name":"7","id":"rs1342306308"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1445923777","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565417,"feature_type":"variation","strand":1,"end":140565417,"alleles":["G","A"]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140565421,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565421,"source":"dbSNP","id":"rs146747071","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565423,"source":"dbSNP","strand":1,"feature_type":"variation","end":140565423,"alleles":["C","T"],"seq_region_name":"7","id":"rs948810524","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797800056","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565426,"source":"dbSNP","strand":1,"feature_type":"variation","end":140565426,"alleles":["T","C"]},{"alleles":["G","T"],"end":140565430,"strand":1,"feature_type":"variation","start":140565430,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs547415914","seq_region_name":"7","clinical_significance":[]},{"start":140565431,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140565431,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1205766409","clinical_significance":[]},{"id":"rs1044598794","seq_region_name":"7","clinical_significance":[],"alleles":["C","G","T"],"end":140565436,"strand":1,"feature_type":"variation","start":140565436,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565439,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140565439,"id":"rs888603020","seq_region_name":"7","clinical_significance":[]},{"start":140565440,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140565440,"alleles":["A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1340992173","clinical_significance":[]},{"start":140565441,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140565441,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797800674","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797800765","source":"dbSNP","start":140565445,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140565445,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1255885739","seq_region_name":"7","feature_type":"variation","strand":1,"end":140565447,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565447},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140565452,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565452,"source":"dbSNP","seq_region_name":"7","id":"rs1229704521","clinical_significance":[]},{"clinical_significance":[],"id":"rs77267272","seq_region_name":"7","source":"dbSNP","start":140565456,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140565456,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs533475309","end":140565459,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140565459,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140565461,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565461,"clinical_significance":[],"seq_region_name":"7","id":"rs979122924"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565464,"source":"dbSNP","strand":1,"feature_type":"variation","end":140565464,"alleles":["T","G"],"seq_region_name":"7","id":"rs1797801488","clinical_significance":[]},{"source":"dbSNP","start":140565467,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140565467,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1442750139"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565475,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140565475,"clinical_significance":[],"seq_region_name":"7","id":"rs1797801696"},{"clinical_significance":[],"id":"rs1797801781","seq_region_name":"7","feature_type":"variation","strand":1,"end":140565476,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565476},{"start":140565480,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140565480,"strand":1,"feature_type":"variation","id":"rs10242266","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs563108113","feature_type":"variation","strand":1,"end":140565482,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565482},{"feature_type":"variation","strand":1,"end":140565487,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565487,"clinical_significance":[],"id":"rs1797802100","seq_region_name":"7"},{"source":"dbSNP","start":140565491,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140565491,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1440137564"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797802319","alleles":["T","A"],"end":140565494,"feature_type":"variation","strand":1,"source":"dbSNP","start":140565494,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797802420","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565497,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140565497},{"source":"dbSNP","start":140565498,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140565498,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1428920856","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140565499,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565499,"clinical_significance":[],"id":"rs1186205030","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1365999823","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565500,"source":"dbSNP","strand":1,"feature_type":"variation","end":140565500,"alleles":["G","A"]},{"feature_type":"variation","strand":1,"end":140565503,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565503,"clinical_significance":[],"seq_region_name":"7","id":"rs1167121091"},{"seq_region_name":"7","id":"rs1797802933","clinical_significance":[],"alleles":["C","A","G"],"end":140565504,"strand":1,"feature_type":"variation","start":140565504,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs373413412","clinical_significance":[],"end":140565505,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140565505,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140565506,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140565506,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1413079923"},{"seq_region_name":"7","id":"rs1797803290","clinical_significance":[],"strand":1,"feature_type":"variation","end":140565508,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565508,"source":"dbSNP"},{"id":"rs956496769","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565515,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140565515},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797803485","source":"dbSNP","start":140565526,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140565526,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797803604","alleles":["C","T"],"end":140565528,"feature_type":"variation","strand":1,"source":"dbSNP","start":140565528,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1797803708","clinical_significance":[],"alleles":["A","G"],"end":140565531,"strand":1,"feature_type":"variation","start":140565531,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140565534,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","start":140565534,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs998262183","clinical_significance":[]},{"clinical_significance":[],"id":"rs1471433364","seq_region_name":"7","feature_type":"variation","strand":1,"end":140565542,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565542},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565547,"source":"dbSNP","strand":1,"feature_type":"variation","end":140565547,"alleles":["T","C"],"id":"rs1168151481","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1250310643","source":"dbSNP","start":140565559,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140565559,"feature_type":"variation","strand":1},{"alleles":["C","T"],"end":140565567,"strand":1,"feature_type":"variation","start":140565567,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs562471462","clinical_significance":[]},{"id":"rs953940370","seq_region_name":"7","clinical_significance":[],"end":140565568,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140565568,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565576,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140565576,"clinical_significance":[],"seq_region_name":"7","id":"rs1797804505"},{"end":140565579,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140565579,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1490604144","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565582,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140565582,"clinical_significance":[],"seq_region_name":"7","id":"rs1585645570"},{"seq_region_name":"7","id":"rs1006627919","clinical_significance":[],"start":140565583,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140565583,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1797804994","clinical_significance":[],"start":140565583,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TTTATTTATTT","TTTATTT"],"end":140565593,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565585,"source":"dbSNP","strand":1,"feature_type":"variation","end":140565585,"alleles":["T","C"],"seq_region_name":"7","id":"rs1022106478","clinical_significance":[]},{"id":"rs2130588557","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565586,"source":"dbSNP","strand":1,"feature_type":"variation","end":140565586,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs1177703401","clinical_significance":[],"strand":1,"feature_type":"variation","end":140565596,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565596,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565602,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140565602,"clinical_significance":[],"id":"rs1223233447","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs549588420","feature_type":"variation","strand":1,"alleles":["A","T"],"end":140565610,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565610},{"seq_region_name":"7","id":"rs967850455","clinical_significance":[],"alleles":["A","G"],"end":140565619,"strand":1,"feature_type":"variation","start":140565619,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["T","C"],"end":140565620,"strand":1,"feature_type":"variation","start":140565620,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs568204986","clinical_significance":[]},{"source":"dbSNP","start":140565621,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140565621,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130588605"},{"id":"rs1797805754","seq_region_name":"7","clinical_significance":[],"start":140565624,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140565624,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1797805870","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565630,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140565630},{"start":140565634,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140565634,"alleles":["T","C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs685182","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565637,"feature_type":"variation","strand":1,"end":140565637,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130588657"},{"id":"rs1288520377","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565639,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140565639},{"feature_type":"variation","strand":1,"end":140565640,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565640,"clinical_significance":[],"seq_region_name":"7","id":"rs1223904519"},{"feature_type":"variation","strand":1,"end":140565641,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565641,"clinical_significance":[],"seq_region_name":"7","id":"rs1563145087"},{"seq_region_name":"7","id":"rs1797806586","clinical_significance":[],"strand":1,"feature_type":"variation","end":140565642,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565642,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797806699","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565645,"feature_type":"variation","strand":1,"end":140565645,"alleles":["T","C"]},{"start":140565647,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140565647,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797806791","clinical_significance":[]},{"id":"rs960619210","seq_region_name":"7","clinical_significance":[],"end":140565651,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140565651,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1394863066","feature_type":"variation","strand":1,"end":140565671,"alleles":["GG","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565670},{"clinical_significance":[],"id":"rs2130588721","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565670,"feature_type":"variation","strand":1,"end":140565706,"alleles":["GGTGTGTGAACCACAGCGAGTCCATCCTGAGTAGGGG","GG"]},{"seq_region_name":"7","id":"rs1797807130","clinical_significance":[],"strand":1,"feature_type":"variation","end":140565671,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565671,"source":"dbSNP"},{"id":"rs190554921","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140565673,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565673,"source":"dbSNP"},{"id":"rs2130588744","seq_region_name":"7","clinical_significance":[],"end":140565675,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140565675,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs917229660","clinical_significance":[],"strand":1,"feature_type":"variation","end":140565680,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565680,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1797807490","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565683,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140565683},{"source":"dbSNP","start":140565686,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140565686,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797807606"},{"seq_region_name":"7","id":"rs1327142569","clinical_significance":[],"alleles":["G","A"],"end":140565687,"strand":1,"feature_type":"variation","start":140565687,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1797807846","seq_region_name":"7","clinical_significance":[],"alleles":["A","G"],"end":140565688,"strand":1,"feature_type":"variation","start":140565688,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140565689,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140565689,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797807944","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797808053","clinical_significance":[],"alleles":["T","A"],"end":140565690,"strand":1,"feature_type":"variation","start":140565690,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1402054864","alleles":["C","T"],"end":140565695,"feature_type":"variation","strand":1,"source":"dbSNP","start":140565695,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs926522042","seq_region_name":"7","source":"dbSNP","start":140565696,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140565696,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1797808371","clinical_significance":[],"strand":1,"feature_type":"variation","end":140565697,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565697,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565705,"source":"dbSNP","strand":1,"feature_type":"variation","end":140565705,"alleles":["G","T"],"seq_region_name":"7","id":"rs759461871","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140565711,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565711,"clinical_significance":[],"seq_region_name":"7","id":"rs1797808607"},{"strand":1,"feature_type":"variation","end":140565715,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565715,"source":"dbSNP","seq_region_name":"7","id":"rs1456581058","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565718,"source":"dbSNP","strand":1,"feature_type":"variation","end":140565718,"alleles":["G","A"],"id":"rs1797808833","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140565719,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140565719,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797808977"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1349574138","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140565720,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565720},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565725,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140565725,"clinical_significance":[],"seq_region_name":"7","id":"rs1797809204"},{"clinical_significance":[],"id":"rs931182036","seq_region_name":"7","alleles":["A","G","T"],"end":140565727,"feature_type":"variation","strand":1,"source":"dbSNP","start":140565727,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797809482","end":140565728,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140565728,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140565730,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565730,"source":"dbSNP","seq_region_name":"7","id":"rs1409888095","clinical_significance":[]},{"seq_region_name":"7","id":"rs1223906391","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565731,"source":"dbSNP","strand":1,"feature_type":"variation","end":140565731,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797809822","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565733,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140565733},{"start":140565741,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140565741,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797809926","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585645832","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565744,"source":"dbSNP","strand":1,"feature_type":"variation","end":140565744,"alleles":["C","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565744,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CCC","CCCC"],"end":140565746,"seq_region_name":"7","id":"rs35878682","clinical_significance":[]},{"clinical_significance":[],"id":"rs1797810250","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565748,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140565748},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140565749,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565749,"clinical_significance":[],"seq_region_name":"7","id":"rs1257602474"},{"clinical_significance":[],"seq_region_name":"7","id":"rs148903441","feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140565750,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565750},{"clinical_significance":[],"seq_region_name":"7","id":"rs1271409627","feature_type":"variation","strand":1,"end":140565759,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565759},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565760,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140565760,"seq_region_name":"7","id":"rs1044482449","clinical_significance":[]},{"alleles":["A","C"],"end":140565762,"strand":1,"feature_type":"variation","start":140565762,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797810853","clinical_significance":[]},{"clinical_significance":[],"id":"rs1585645897","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565772,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140565772},{"start":140565773,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140565773,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs539372323","clinical_significance":[]},{"alleles":["G","A","T"],"end":140565774,"feature_type":"variation","strand":1,"source":"dbSNP","start":140565774,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs910092021"},{"seq_region_name":"7","id":"rs1797811301","clinical_significance":[],"strand":1,"feature_type":"variation","end":140565775,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565775,"source":"dbSNP"},{"alleles":["C","A"],"end":140565776,"feature_type":"variation","strand":1,"source":"dbSNP","start":140565776,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs941502558","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565778,"feature_type":"variation","strand":1,"end":140565778,"alleles":["C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1191011863"},{"end":140565785,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140565785,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797811638","clinical_significance":[]},{"seq_region_name":"7","id":"rs1262029875","clinical_significance":[],"alleles":["C","T"],"end":140565787,"strand":1,"feature_type":"variation","start":140565787,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140565787,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140565787,"alleles":["C","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797811838"},{"alleles":["G","A"],"end":140565788,"strand":1,"feature_type":"variation","start":140565788,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1265712020","clinical_significance":[]},{"id":"rs1227642821","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565789,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140565789},{"seq_region_name":"7","id":"rs1797812031","clinical_significance":[],"strand":1,"feature_type":"variation","end":140565792,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565792,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1585645976","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140565793,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565793,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1797812253","seq_region_name":"7","source":"dbSNP","start":140565797,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140565797,"feature_type":"variation","strand":1},{"id":"rs1037161956","seq_region_name":"7","clinical_significance":[],"start":140565802,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140565802,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"start":140565803,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G","T"],"end":140565803,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs776850229","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797812598","clinical_significance":[],"start":140565804,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140565804,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140565807,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565807,"source":"dbSNP","seq_region_name":"7","id":"rs1797812690","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565808,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AAAA","AAA"],"end":140565811,"seq_region_name":"7","id":"rs1384909998","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1367132728","feature_type":"variation","strand":1,"end":140565812,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565812},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565815,"source":"dbSNP","strand":1,"feature_type":"variation","end":140565815,"alleles":["G","C","T"],"id":"rs1289626612","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140565816,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140565816,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797813174"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140565817,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565817,"clinical_significance":[],"seq_region_name":"7","id":"rs1797813318"},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140565825,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565825,"source":"dbSNP","seq_region_name":"7","id":"rs1797813422","clinical_significance":[]},{"clinical_significance":[],"id":"rs1797813512","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565827,"feature_type":"variation","strand":1,"end":140565827,"alleles":["A","C"]},{"clinical_significance":[],"id":"rs1041097415","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140565831,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565831},{"seq_region_name":"7","id":"rs557993318","clinical_significance":[],"strand":1,"feature_type":"variation","end":140565832,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565832,"source":"dbSNP"},{"end":140565835,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140565835,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130589213"},{"id":"rs1464957593","seq_region_name":"7","clinical_significance":[],"start":140565838,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140565838,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565839,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140565839,"clinical_significance":[],"id":"rs1158521975","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797814098","feature_type":"variation","strand":1,"end":140565845,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565845},{"strand":1,"feature_type":"variation","end":140565847,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565847,"source":"dbSNP","seq_region_name":"7","id":"rs901386818","clinical_significance":[]},{"id":"rs1172556479","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140565849,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565849,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565851,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140565851,"seq_region_name":"7","id":"rs996969651","clinical_significance":[]},{"alleles":["A","AA"],"end":140565855,"strand":1,"feature_type":"variation","start":140565855,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797814590","clinical_significance":[]},{"source":"dbSNP","start":140565856,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140565856,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797814694"},{"seq_region_name":"7","id":"rs998418572","clinical_significance":[],"start":140565862,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A","C"],"end":140565862,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140565863,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565863,"source":"dbSNP","seq_region_name":"7","id":"rs1432927965","clinical_significance":[]},{"seq_region_name":"7","id":"rs1385699927","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140565865,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565865,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1421596272","alleles":["G","C","T"],"end":140565867,"feature_type":"variation","strand":1,"source":"dbSNP","start":140565867,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140565871,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565871,"source":"dbSNP","id":"rs142753544","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1360115942","source":"dbSNP","start":140565872,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140565872,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs529374923","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565874,"source":"dbSNP","strand":1,"feature_type":"variation","end":140565874,"alleles":["C","G"]},{"seq_region_name":"7","id":"rs889438890","clinical_significance":[],"start":140565877,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140565877,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1006632595","clinical_significance":[],"start":140565878,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140565878,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs969005058","feature_type":"variation","strand":1,"end":140565882,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565882},{"clinical_significance":[],"seq_region_name":"7","id":"rs151047151","feature_type":"variation","strand":1,"alleles":["C","A","G"],"end":140565883,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565883},{"start":140565885,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140565885,"strand":1,"feature_type":"variation","id":"rs1303093587","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","G"],"end":140565886,"feature_type":"variation","strand":1,"source":"dbSNP","start":140565886,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797816219"},{"id":"rs1231012491","seq_region_name":"7","clinical_significance":[],"start":140565893,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140565893,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140565894,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565894,"clinical_significance":[],"seq_region_name":"7","id":"rs1797816443"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130589423","end":140565895,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140565895,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140565896,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140565896,"strand":1,"feature_type":"variation","id":"rs1797816549","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs561524570","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565897,"feature_type":"variation","strand":1,"end":140565897,"alleles":["C","T"]},{"alleles":["C","T"],"end":140565899,"strand":1,"feature_type":"variation","start":140565899,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130589439","clinical_significance":[]},{"seq_region_name":"7","id":"rs1274068226","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140565901,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565901,"source":"dbSNP"},{"source":"dbSNP","start":140565904,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140565904,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1805679969"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565907,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140565907,"seq_region_name":"7","id":"rs1311340935","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565909,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140565909,"clinical_significance":[],"seq_region_name":"7","id":"rs1797816942"},{"source":"dbSNP","start":140565910,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140565910,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1032026215"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797817161","feature_type":"variation","strand":1,"alleles":["T","-"],"end":140565910,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565910},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565917,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140565917,"clinical_significance":[],"seq_region_name":"7","id":"rs1797817273"},{"feature_type":"variation","strand":1,"end":140565919,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565919,"clinical_significance":[],"seq_region_name":"7","id":"rs1329180270"},{"id":"rs573832750","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140565924,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565924,"source":"dbSNP"},{"clinical_significance":[],"id":"rs10245737","seq_region_name":"7","feature_type":"variation","strand":1,"end":140565925,"alleles":["G","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565925},{"clinical_significance":[],"id":"rs1585646318","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565926,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140565926},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797817825","source":"dbSNP","start":140565928,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140565928,"feature_type":"variation","strand":1},{"end":140565931,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140565931,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1319954465","seq_region_name":"7","clinical_significance":[]},{"id":"rs2130589555","seq_region_name":"7","clinical_significance":[],"end":140565936,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140565936,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140565938,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565938,"source":"dbSNP","id":"rs2109925","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565941,"source":"dbSNP","strand":1,"feature_type":"variation","end":140565941,"alleles":["G","A"],"id":"rs1797818245","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1030812983","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140565944,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565944,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1213846878","clinical_significance":[],"strand":1,"feature_type":"variation","end":140565953,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565953,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565956,"feature_type":"variation","strand":1,"end":140565956,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs960922641"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140565962,"feature_type":"variation","strand":1,"end":140565962,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1301554531"},{"source":"dbSNP","start":140565966,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140565966,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs2130589622","seq_region_name":"7"},{"alleles":["A","G"],"end":140565974,"strand":1,"feature_type":"variation","start":140565974,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1024721093","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565977,"source":"dbSNP","strand":1,"feature_type":"variation","end":140565982,"alleles":["AATAAT","AAT"],"seq_region_name":"7","id":"rs1373933823","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140565985,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565985,"source":"dbSNP","seq_region_name":"7","id":"rs970588864","clinical_significance":[]},{"seq_region_name":"7","id":"rs1450932687","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140565990,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TT","T"],"end":140565991},{"seq_region_name":"7","id":"rs533313497","clinical_significance":[],"start":140565991,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140565991,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140565998,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140565998,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797819349"},{"seq_region_name":"7","id":"rs146601288","clinical_significance":[],"start":140565999,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140565999,"strand":1,"feature_type":"variation"},{"alleles":["T","C"],"end":140566000,"strand":1,"feature_type":"variation","start":140566000,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1187349368","clinical_significance":[]},{"source":"dbSNP","start":140566002,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140566002,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797819927"},{"id":"rs980601066","seq_region_name":"7","clinical_significance":[],"end":140566003,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140566003,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs992077856","clinical_significance":[],"alleles":["A","C"],"end":140566007,"strand":1,"feature_type":"variation","start":140566007,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140566016,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140566016,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797820471"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566019,"source":"dbSNP","strand":1,"feature_type":"variation","end":140566019,"alleles":["C","T"],"seq_region_name":"7","id":"rs1198599683","clinical_significance":[]},{"source":"dbSNP","start":140566020,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140566024,"alleles":["AAAAA","AAAAAA"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1797820829","seq_region_name":"7"},{"seq_region_name":"7","id":"rs183098372","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566023,"source":"dbSNP","strand":1,"feature_type":"variation","end":140566023,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs1797821177","clinical_significance":[],"start":140566026,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140566026,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140566027,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566027,"clinical_significance":[],"id":"rs1797821295","seq_region_name":"7"},{"id":"rs1251667199","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566032,"source":"dbSNP","strand":1,"feature_type":"variation","end":140566032,"alleles":["C","T"]},{"strand":1,"feature_type":"variation","end":140566037,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566037,"source":"dbSNP","id":"rs931258143","seq_region_name":"7","clinical_significance":[]},{"start":140566040,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140566040,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs970082913","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs564048930","source":"dbSNP","start":140566041,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140566041,"alleles":["C","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797821847","source":"dbSNP","start":140566044,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140566044,"alleles":["A","G"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140566046,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566046,"source":"dbSNP","seq_region_name":"7","id":"rs1797821962","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140566048,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566048,"clinical_significance":[],"seq_region_name":"7","id":"rs1797822089"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797822189","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566049,"feature_type":"variation","strand":1,"end":140566049,"alleles":["T","C"]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140566050,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566050,"clinical_significance":[],"seq_region_name":"7","id":"rs984419697"},{"seq_region_name":"7","id":"rs1797822392","clinical_significance":[],"alleles":["T","C"],"end":140566051,"strand":1,"feature_type":"variation","start":140566051,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566055,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140566055,"seq_region_name":"7","id":"rs1340271590","clinical_significance":[]},{"seq_region_name":"7","id":"rs1297092449","clinical_significance":[],"end":140566059,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140566059,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1247020003","source":"dbSNP","start":140566062,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140566062,"alleles":["G","A","C"],"feature_type":"variation","strand":1},{"end":140566064,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140566064,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2109926"},{"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140566065,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566065,"source":"dbSNP","seq_region_name":"7","id":"rs1797822990","clinical_significance":[]},{"end":140566068,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140566068,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797823098","clinical_significance":[]},{"clinical_significance":[],"id":"rs909976376","seq_region_name":"7","end":140566077,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140566077,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140566078,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140566078,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs941401556","clinical_significance":[]},{"id":"rs1041154019","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140566085,"alleles":["TTCCTTT","TT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566079,"source":"dbSNP"},{"end":140566080,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140566080,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1797823515","seq_region_name":"7"},{"start":140566082,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140566082,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1442147191","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797823726","end":140566085,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140566085,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1310218855","clinical_significance":[],"alleles":["C","T"],"end":140566087,"strand":1,"feature_type":"variation","start":140566087,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566092,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140566092,"clinical_significance":[],"id":"rs1428269484","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140566093,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566093,"clinical_significance":[],"seq_region_name":"7","id":"rs901270852"},{"clinical_significance":[],"seq_region_name":"7","id":"rs932704575","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566094,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140566094},{"start":140566095,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140566095,"alleles":["A","C","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1049898610","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140566096,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566096,"clinical_significance":[],"seq_region_name":"7","id":"rs1797824444"},{"seq_region_name":"7","id":"rs1797824563","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566102,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140566102},{"alleles":["C","T"],"end":140566103,"strand":1,"feature_type":"variation","start":140566103,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1797824676","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","A","T"],"end":140566105,"strand":1,"feature_type":"variation","start":140566105,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs187773418","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140566107,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566107,"clinical_significance":[],"seq_region_name":"7","id":"rs1423159730"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797825044","end":140566110,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140566110,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566113,"feature_type":"variation","strand":1,"end":140566113,"alleles":["G","A","C"],"clinical_significance":[],"id":"rs1032325900","seq_region_name":"7"},{"end":140566119,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140566119,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs756561533","clinical_significance":[]},{"end":140566124,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140566124,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797825465"},{"seq_region_name":"7","id":"rs1797825585","clinical_significance":[],"end":140566125,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140566125,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140566128,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140566128,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1295522194","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1273666887","source":"dbSNP","start":140566131,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140566131,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs752492739","end":140566134,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140566134,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["C","-"],"end":140566134,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566134,"source":"dbSNP","seq_region_name":"7","id":"rs1797826049","clinical_significance":[]},{"start":140566135,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140566135,"strand":1,"feature_type":"variation","id":"rs1797826160","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1263750463","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140566138,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566138,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1024605144","clinical_significance":[],"start":140566139,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140566139,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1244222015","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566140,"feature_type":"variation","strand":1,"end":140566140,"alleles":["T","C"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566141,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140566141,"clinical_significance":[],"seq_region_name":"7","id":"rs1797826337"},{"seq_region_name":"7","id":"rs934258817","clinical_significance":[],"strand":1,"feature_type":"variation","end":140566142,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566142,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1051348204","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140566143,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566143,"source":"dbSNP"},{"seq_region_name":"7","id":"rs889482230","clinical_significance":[],"alleles":["G","A","T"],"end":140566144,"strand":1,"feature_type":"variation","start":140566144,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["C","T"],"end":140566145,"feature_type":"variation","strand":1,"source":"dbSNP","start":140566145,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1290710510","seq_region_name":"7"},{"seq_region_name":"7","id":"rs980488193","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566150,"source":"dbSNP","strand":1,"feature_type":"variation","end":140566150,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs942375994","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566151,"feature_type":"variation","strand":1,"end":140566151,"alleles":["C","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566154,"source":"dbSNP","strand":1,"feature_type":"variation","end":140566154,"alleles":["C","A"],"id":"rs1350190156","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566155,"feature_type":"variation","strand":1,"end":140566155,"alleles":["C","T"],"clinical_significance":[],"id":"rs1043333127","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs903632499","source":"dbSNP","start":140566156,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140566156,"alleles":["T","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1379011914","alleles":["G","A"],"end":140566157,"feature_type":"variation","strand":1,"source":"dbSNP","start":140566157,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566159,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140566159,"clinical_significance":[],"seq_region_name":"7","id":"rs546235165"},{"alleles":["T","C"],"end":140566164,"feature_type":"variation","strand":1,"source":"dbSNP","start":140566164,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1307860508"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566165,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140566165,"clinical_significance":[],"id":"rs1392506675","seq_region_name":"7"},{"clinical_significance":[],"id":"rs141712338","seq_region_name":"7","source":"dbSNP","start":140566166,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140566166,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140566167,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566167,"source":"dbSNP","id":"rs1797827967","seq_region_name":"7","clinical_significance":[]},{"start":140566168,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140566168,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs984090206","clinical_significance":[]},{"start":140566172,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140566172,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1246473395","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140566175,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566175,"clinical_significance":[],"seq_region_name":"7","id":"rs1797828297"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566176,"source":"dbSNP","strand":1,"feature_type":"variation","end":140566176,"alleles":["C","T"],"seq_region_name":"7","id":"rs867482039","clinical_significance":[]},{"seq_region_name":"7","id":"rs10246080","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566177,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140566177},{"seq_region_name":"7","id":"rs1013961326","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566178,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140566178},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140566182,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566182,"source":"dbSNP","seq_region_name":"7","id":"rs2130590257","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566183,"feature_type":"variation","strand":1,"end":140566183,"alleles":["C","T"],"clinical_significance":[],"id":"rs1797828863","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140566184,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566184,"clinical_significance":[],"seq_region_name":"7","id":"rs1023546479"},{"seq_region_name":"7","id":"rs1209602673","clinical_significance":[],"start":140566185,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140566185,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566188,"feature_type":"variation","strand":1,"end":140566188,"alleles":["C","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs60872627"},{"alleles":["G","A"],"end":140566189,"feature_type":"variation","strand":1,"source":"dbSNP","start":140566189,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs374491024"},{"seq_region_name":"7","id":"rs1265589844","clinical_significance":[],"end":140566206,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140566206,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1797829641","seq_region_name":"7","source":"dbSNP","start":140566209,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140566209,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140566211,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566211,"clinical_significance":[],"seq_region_name":"7","id":"rs1797829749"},{"id":"rs1797829870","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566216,"source":"dbSNP","strand":1,"feature_type":"variation","end":140566216,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs749851909","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566219,"source":"dbSNP","strand":1,"feature_type":"variation","end":140566219,"alleles":["A","C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797830126","alleles":["G","T"],"end":140566223,"feature_type":"variation","strand":1,"source":"dbSNP","start":140566223,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140566229,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566229,"source":"dbSNP","seq_region_name":"7","id":"rs539461584","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1329877409","feature_type":"variation","strand":1,"end":140566232,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566232},{"clinical_significance":[],"seq_region_name":"7","id":"rs932758514","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566233,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140566233},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566237,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140566237,"clinical_significance":[],"id":"rs1797830605","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1585647131","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140566239,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566239,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140566252,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566252,"clinical_significance":[],"seq_region_name":"7","id":"rs1797830811"},{"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140566254,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566254,"clinical_significance":[],"seq_region_name":"7","id":"rs1797830937"},{"end":140566255,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140566255,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1648918943","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797831054","source":"dbSNP","start":140566257,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140566257,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1016916071","clinical_significance":[],"start":140566274,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140566274,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs769264940","clinical_significance":[],"start":140566275,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140566275,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1379713764","clinical_significance":[],"end":140566277,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140566277,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["T","C"],"end":140566282,"strand":1,"feature_type":"variation","start":140566282,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1797831536","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs10952751","clinical_significance":[],"alleles":["C","A","T"],"end":140566283,"strand":1,"feature_type":"variation","start":140566283,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140566284,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566284,"source":"dbSNP","seq_region_name":"7","id":"rs1797831931","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566291,"source":"dbSNP","strand":1,"feature_type":"variation","end":140566291,"alleles":["C","T"],"seq_region_name":"7","id":"rs555524931","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140566295,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566295,"source":"dbSNP","seq_region_name":"7","id":"rs1321122932","clinical_significance":[]},{"alleles":["A","G"],"end":140566297,"feature_type":"variation","strand":1,"source":"dbSNP","start":140566297,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585647206"},{"end":140566299,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140566299,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797832355","clinical_significance":[]},{"alleles":["G","A"],"end":140566300,"strand":1,"feature_type":"variation","start":140566300,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs936158032","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","T"],"end":140566301,"strand":1,"feature_type":"variation","start":140566301,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1563145516","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797832576","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566307,"source":"dbSNP","strand":1,"feature_type":"variation","end":140566307,"alleles":["C","T"]},{"id":"rs2159796","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140566311,"strand":1,"feature_type":"variation","start":140566311,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs555161507","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566312,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140566312},{"alleles":["A","G"],"end":140566315,"feature_type":"variation","strand":1,"source":"dbSNP","start":140566315,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1168280241"},{"start":140566316,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140566316,"strand":1,"feature_type":"variation","id":"rs1797833123","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140566317,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566317,"source":"dbSNP","seq_region_name":"7","id":"rs1585647289","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566319,"feature_type":"variation","strand":1,"end":140566319,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs911478345"},{"seq_region_name":"7","id":"rs573476353","clinical_significance":[],"start":140566320,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140566320,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566321,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140566321,"seq_region_name":"7","id":"rs191270094","clinical_significance":[]},{"id":"rs1043388587","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140566322,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566322,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs147993781","feature_type":"variation","strand":1,"end":140566323,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566323},{"clinical_significance":[],"seq_region_name":"7","id":"rs903517748","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566324,"feature_type":"variation","strand":1,"end":140566324,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1797834537","clinical_significance":[],"alleles":["C","T"],"end":140566325,"strand":1,"feature_type":"variation","start":140566325,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1465515163","source":"dbSNP","start":140566331,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140566331,"feature_type":"variation","strand":1},{"id":"rs1797834842","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["CTT","-"],"end":140566336,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566334,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1382836342","end":140566335,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140566335,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1249972597","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566340,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140566340},{"start":140566345,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140566345,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797835315","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797835429","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566353,"source":"dbSNP","strand":1,"feature_type":"variation","end":140566353,"alleles":["T","C"]},{"id":"rs1585647423","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140566355,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566355,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566357,"feature_type":"variation","strand":1,"alleles":["TTT","TT"],"end":140566359,"clinical_significance":[],"seq_region_name":"7","id":"rs1206969013"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585647439","feature_type":"variation","strand":1,"end":140566362,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566362},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566362,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TTTT","TTTTT"],"end":140566365,"seq_region_name":"7","id":"rs1797835881","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130590661","alleles":["C","T"],"end":140566368,"feature_type":"variation","strand":1,"source":"dbSNP","start":140566368,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140566372,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140566372,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130590666"},{"source":"dbSNP","start":140566378,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140566378,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs935107395"},{"seq_region_name":"7","id":"rs756830207","clinical_significance":[],"alleles":["G","A"],"end":140566379,"strand":1,"feature_type":"variation","start":140566379,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs896344840","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566381,"feature_type":"variation","strand":1,"end":140566381,"alleles":["C","T"]},{"feature_type":"variation","strand":1,"end":140566383,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566383,"clinical_significance":[],"seq_region_name":"7","id":"rs1015393969"},{"clinical_significance":[],"seq_region_name":"7","id":"rs578025250","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140566384,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566384},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566386,"feature_type":"variation","strand":1,"end":140566386,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1797836646"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797836776","alleles":["TT","T"],"end":140566388,"feature_type":"variation","strand":1,"source":"dbSNP","start":140566387,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140566389,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566389,"source":"dbSNP","seq_region_name":"7","id":"rs1639963","clinical_significance":[]},{"end":140566391,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140566391,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1797837014","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566392,"source":"dbSNP","strand":1,"feature_type":"variation","end":140566392,"alleles":["T","C"],"seq_region_name":"7","id":"rs1233104861","clinical_significance":[]},{"source":"dbSNP","start":140566396,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140566396,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs184515756"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1320737321","end":140566400,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140566400,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140566407,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140566407,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs976616570","clinical_significance":[]},{"id":"rs1387321144","seq_region_name":"7","clinical_significance":[],"start":140566408,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140566408,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"start":140566411,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140566411,"alleles":["A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585647573","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs922630132","feature_type":"variation","strand":1,"end":140566413,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566413},{"seq_region_name":"7","id":"rs1013428365","clinical_significance":[],"alleles":["C","T"],"end":140566414,"strand":1,"feature_type":"variation","start":140566414,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140566415,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140566415,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1023850648"},{"seq_region_name":"7","id":"rs563648011","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140566417,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566417,"source":"dbSNP"},{"source":"dbSNP","start":140566424,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140566424,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1450309751"},{"seq_region_name":"7","id":"rs1639964","clinical_significance":[],"start":140566426,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140566426,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566429,"source":"dbSNP","strand":1,"feature_type":"variation","end":140566429,"alleles":["G","T"],"seq_region_name":"7","id":"rs1797838420","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585647634","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140566437,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566437},{"id":"rs531264076","seq_region_name":"7","clinical_significance":[],"start":140566439,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140566439,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566444,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140566444,"id":"rs1016969538","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566449,"source":"dbSNP","strand":1,"feature_type":"variation","end":140566449,"alleles":["A","T"],"seq_region_name":"7","id":"rs2130590861","clinical_significance":[]},{"start":140566450,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140566450,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1197254977","clinical_significance":[]},{"end":140566458,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140566458,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1797839000","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566460,"feature_type":"variation","strand":1,"end":140566460,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1797839099"},{"seq_region_name":"7","id":"rs1797839211","clinical_significance":[],"start":140566462,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140566462,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs188211479","seq_region_name":"7","feature_type":"variation","strand":1,"end":140566465,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566465},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797839469","source":"dbSNP","start":140566466,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140566466,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1448897862","clinical_significance":[],"start":140566467,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140566467,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1639965","seq_region_name":"7","source":"dbSNP","start":140566479,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140566479,"alleles":["A","C"],"feature_type":"variation","strand":1},{"start":140566481,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140566481,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585647732","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs973260612","feature_type":"variation","strand":1,"end":140566489,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566489},{"start":140566490,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140566490,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1025733678","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566495,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140566495,"clinical_significance":[],"seq_region_name":"7","id":"rs2130590942"},{"end":140566500,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140566500,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797840183","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797840311","end":140566501,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140566501,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["A","G"],"end":140566505,"strand":1,"feature_type":"variation","start":140566505,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1797840431","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","C"],"end":140566509,"feature_type":"variation","strand":1,"source":"dbSNP","start":140566509,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1212777860"},{"seq_region_name":"7","id":"rs1441261712","clinical_significance":[],"start":140566512,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140566512,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140566514,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140566514,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1797840772","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1797840879","clinical_significance":[],"alleles":["A","G"],"end":140566517,"strand":1,"feature_type":"variation","start":140566517,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140566518,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140566518,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797840989","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797841098","clinical_significance":[],"start":140566519,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","-"],"end":140566519,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140566523,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566523,"source":"dbSNP","seq_region_name":"7","id":"rs1183662133","clinical_significance":[]},{"id":"rs1797841329","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140566524,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566524,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566531,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140566531,"id":"rs1206383813","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566532,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140566532,"clinical_significance":[],"seq_region_name":"7","id":"rs1797841553"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566537,"feature_type":"variation","strand":1,"end":140566537,"alleles":["G","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1797841732"},{"source":"dbSNP","start":140566542,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140566542,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130591028"},{"clinical_significance":[],"seq_region_name":"7","id":"rs771638900","feature_type":"variation","strand":1,"end":140566545,"alleles":["GGGG","GGG"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566542},{"alleles":["G","C"],"end":140566543,"feature_type":"variation","strand":1,"source":"dbSNP","start":140566543,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1342401282"},{"source":"dbSNP","start":140566549,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140566549,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797842317"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566551,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140566551,"clinical_significance":[],"seq_region_name":"7","id":"rs1299309603"},{"strand":1,"feature_type":"variation","end":140566560,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566560,"source":"dbSNP","seq_region_name":"7","id":"rs1797842667","clinical_significance":[]},{"clinical_significance":[],"id":"rs114776652","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566561,"feature_type":"variation","strand":1,"end":140566561,"alleles":["A","T"]},{"strand":1,"feature_type":"variation","end":140566565,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566565,"source":"dbSNP","seq_region_name":"7","id":"rs1639966","clinical_significance":[]},{"alleles":["T","C"],"end":140566566,"feature_type":"variation","strand":1,"source":"dbSNP","start":140566566,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1797843187","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566575,"feature_type":"variation","strand":1,"end":140566575,"alleles":["T","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585647827"},{"id":"rs955600473","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566576,"source":"dbSNP","strand":1,"feature_type":"variation","end":140566576,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563145673","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140566582,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566582},{"clinical_significance":[],"seq_region_name":"7","id":"rs1360590804","feature_type":"variation","strand":1,"end":140566586,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566586},{"clinical_significance":[],"id":"rs1797844017","seq_region_name":"7","source":"dbSNP","start":140566587,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140566587,"alleles":["G","T"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140566588,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566588,"source":"dbSNP","id":"rs1797844114","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797844249","clinical_significance":[],"start":140566595,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140566595,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566598,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140566598,"clinical_significance":[],"seq_region_name":"7","id":"rs528648478"},{"seq_region_name":"7","id":"rs1450117711","clinical_significance":[],"end":140566601,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140566601,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140566614,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566614,"clinical_significance":[],"id":"rs533008588","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1797844715","clinical_significance":[],"start":140566618,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140566618,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs964294017","feature_type":"variation","strand":1,"end":140566627,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566627},{"source":"dbSNP","start":140566629,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140566629,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797844940"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566630,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140566630,"seq_region_name":"7","id":"rs370107450","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566633,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140566633,"seq_region_name":"7","id":"rs1797845178","clinical_significance":[]},{"clinical_significance":[],"id":"rs950297969","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566635,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140566635},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566636,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140566636,"seq_region_name":"7","id":"rs924990829","clinical_significance":[]},{"source":"dbSNP","start":140566638,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140566638,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1797845526","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566643,"feature_type":"variation","strand":1,"end":140566643,"alleles":["A","G"],"clinical_significance":[],"id":"rs1045995910","seq_region_name":"7"},{"start":140566651,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140566651,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797845751","clinical_significance":[]},{"source":"dbSNP","start":140566652,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140566652,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130591248"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140566654,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566654,"source":"dbSNP","seq_region_name":"7","id":"rs906234283","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs556733008","feature_type":"variation","strand":1,"end":140566659,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566659},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566661,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140566661,"clinical_significance":[],"id":"rs1797846091","seq_region_name":"7"},{"id":"rs2130591274","seq_region_name":"7","clinical_significance":[],"start":140566663,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140566663,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140566667,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566667,"clinical_significance":[],"id":"rs934990893","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585647963","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566674,"feature_type":"variation","strand":1,"end":140566674,"alleles":["T","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1472083584","end":140566675,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140566675,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566677,"source":"dbSNP","strand":1,"feature_type":"variation","end":140566677,"alleles":["C","T"],"id":"rs1797846559","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140566680,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566680,"source":"dbSNP","id":"rs1797846678","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797846777","feature_type":"variation","strand":1,"end":140566681,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566681},{"start":140566682,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140566682,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1315835796","clinical_significance":[]},{"alleles":["T","A"],"end":140566683,"strand":1,"feature_type":"variation","start":140566683,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1169792205","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1463897785","clinical_significance":[],"start":140566683,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","TTTTT","TTTTTT"],"end":140566683,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566684,"source":"dbSNP","strand":1,"feature_type":"variation","end":140566684,"alleles":["A","-"],"id":"rs1183580937","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1325485757","clinical_significance":[],"start":140566684,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140566684,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566685,"feature_type":"variation","strand":1,"alleles":["-","C"],"end":140566684,"clinical_significance":[],"seq_region_name":"7","id":"rs1168105030"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566685,"feature_type":"variation","strand":1,"end":140566685,"alleles":["T","C"],"clinical_significance":[],"id":"rs1406714488","seq_region_name":"7"},{"alleles":["T","TGTTTT"],"end":140566685,"strand":1,"feature_type":"variation","start":140566685,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797847797","clinical_significance":[]},{"end":140566688,"alleles":["TTTT","TTTTGTTTT"],"strand":1,"feature_type":"variation","start":140566685,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797847921","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs3043058","feature_type":"variation","strand":1,"alleles":["TTTTTTTTTTTTTTTTTTTT","TTTTTTTTT","TTTTTTTTTT","TTTTTTTTTTT","TTTTTTTTTTTTT","TTTTTTTTTTTTTT","TTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT"],"end":140566704,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566685},{"seq_region_name":"7","id":"rs1797849016","clinical_significance":[],"strand":1,"feature_type":"variation","end":140566686,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566686,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797849133","end":140566687,"alleles":["-","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140566688,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs2130591499","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566690,"feature_type":"variation","strand":1,"alleles":["-","C"],"end":140566689},{"alleles":["T","A"],"end":140566691,"strand":1,"feature_type":"variation","start":140566691,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1002276098","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1054760539","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566693,"feature_type":"variation","strand":1,"alleles":["-","C"],"end":140566692},{"end":140566704,"alleles":["TTT","TTTATTT"],"strand":1,"feature_type":"variation","start":140566702,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs888200942","clinical_significance":[]},{"start":140566704,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140566704,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797849853","clinical_significance":[]},{"source":"dbSNP","start":140566704,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140566705,"alleles":["TG","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797850014"},{"clinical_significance":[],"id":"rs1797850197","seq_region_name":"7","alleles":["-","TTTA","TTTTG","TTTTTA","TTTTTG","TTTTTTA","TTTTTTTA","TTTTTTTTA"],"end":140566704,"feature_type":"variation","strand":1,"source":"dbSNP","start":140566705,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1218773999","seq_region_name":"7","clinical_significance":[],"alleles":["G","T"],"end":140566705,"strand":1,"feature_type":"variation","start":140566705,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140566705,"alleles":["G","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566705,"clinical_significance":[],"seq_region_name":"7","id":"rs1797850794"},{"seq_region_name":"7","id":"rs2130591576","clinical_significance":[],"start":140566705,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140566708,"alleles":["GAGA","GA"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140566713,"alleles":["GAGACGGAG","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566705,"source":"dbSNP","seq_region_name":"7","id":"rs1797850957","clinical_significance":[]},{"start":140566705,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["GAGACGGAG","-"],"end":140566713,"strand":1,"feature_type":"variation","id":"rs1797851075","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1279481187","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566706,"feature_type":"variation","strand":1,"end":140566706,"alleles":["A","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566707,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140566707,"clinical_significance":[],"id":"rs1321342388","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1382387963","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["-","TT","TTTTT"],"end":140566707,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566708,"source":"dbSNP"},{"id":"rs1797851578","seq_region_name":"7","clinical_significance":[],"start":140566709,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","T"],"end":140566709,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1246966272","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566710,"feature_type":"variation","strand":1,"end":140566710,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1223358481","clinical_significance":[],"start":140566711,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140566711,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566712,"feature_type":"variation","strand":1,"end":140566712,"alleles":["A","G","T"],"clinical_significance":[],"id":"rs1585648228","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797852029","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140566713,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566713},{"alleles":["T","A"],"end":140566714,"strand":1,"feature_type":"variation","start":140566714,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797852151","clinical_significance":[]},{"alleles":["TTTT","TTTTTTT"],"end":140566717,"strand":1,"feature_type":"variation","start":140566714,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797852264","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566715,"feature_type":"variation","strand":1,"end":140566715,"alleles":["T","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1554469874"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585648243","feature_type":"variation","strand":1,"end":140566716,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566716},{"id":"rs1052498410","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566718,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C","T"],"end":140566718},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566719,"feature_type":"variation","strand":1,"end":140566719,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1797852762"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1217202785","source":"dbSNP","start":140566721,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140566721,"alleles":["C","T"],"feature_type":"variation","strand":1},{"start":140566725,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","T"],"end":140566725,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1257889303","clinical_significance":[]},{"source":"dbSNP","start":140566726,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140566726,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs569053942"},{"feature_type":"variation","strand":1,"end":140566730,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566730,"clinical_significance":[],"seq_region_name":"7","id":"rs1015864002"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1331215070","source":"dbSNP","start":140566734,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140566734,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs565816742","source":"dbSNP","start":140566735,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140566735,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1044934732","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140566736,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566736},{"clinical_significance":[],"seq_region_name":"7","id":"rs1368083041","alleles":["A","C","G"],"end":140566737,"feature_type":"variation","strand":1,"source":"dbSNP","start":140566737,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1797853873","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566738,"source":"dbSNP","strand":1,"feature_type":"variation","end":140566738,"alleles":["G","A"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566739,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140566739,"seq_region_name":"7","id":"rs594215","clinical_significance":[]},{"clinical_significance":[],"id":"rs1482980330","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140566740,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566740},{"alleles":["A","G"],"end":140566742,"feature_type":"variation","strand":1,"source":"dbSNP","start":140566742,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs192766867","seq_region_name":"7"},{"id":"rs1797854441","seq_region_name":"7","clinical_significance":[],"start":140566744,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140566744,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs954082817","clinical_significance":[],"strand":1,"feature_type":"variation","end":140566747,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566747,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs557971541","end":140566748,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140566748,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs746334284","alleles":["G","A"],"end":140566750,"feature_type":"variation","strand":1,"source":"dbSNP","start":140566750,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140566751,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566751,"source":"dbSNP","seq_region_name":"7","id":"rs1158793335","clinical_significance":[]},{"clinical_significance":[],"id":"rs1797855022","seq_region_name":"7","source":"dbSNP","start":140566755,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140566755,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs2130591866","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566760,"feature_type":"variation","strand":1,"end":140566760,"alleles":["C","T"]},{"source":"dbSNP","start":140566761,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140566761,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1434083205"},{"id":"rs897710044","seq_region_name":"7","clinical_significance":[],"end":140566772,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140566772,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1425657022","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140566774,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566774},{"feature_type":"variation","strand":1,"end":140566790,"alleles":["GGTTCAAGCG","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566781,"clinical_significance":[],"seq_region_name":"7","id":"rs1427719928"},{"source":"dbSNP","start":140566782,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140566782,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797855631"},{"id":"rs2130591918","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140566784,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566784,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566789,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140566789,"seq_region_name":"7","id":"rs994182334","clinical_significance":[]},{"source":"dbSNP","start":140566790,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140566790,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1434813475"},{"clinical_significance":[],"id":"rs1797855952","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140566793,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566793},{"seq_region_name":"7","id":"rs1251823563","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566796,"source":"dbSNP","strand":1,"feature_type":"variation","end":140566796,"alleles":["C","T"]},{"alleles":["T","G"],"end":140566798,"feature_type":"variation","strand":1,"source":"dbSNP","start":140566798,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1563145860"},{"alleles":["G","A"],"end":140566799,"feature_type":"variation","strand":1,"source":"dbSNP","start":140566799,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797856248"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797856354","source":"dbSNP","start":140566800,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140566800,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566803,"source":"dbSNP","strand":1,"feature_type":"variation","end":140566803,"alleles":["C","T"],"seq_region_name":"7","id":"rs1208862462","clinical_significance":[]},{"end":140566805,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140566805,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1681797"},{"start":140566806,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140566806,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs184978285","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140566807,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566807,"source":"dbSNP","seq_region_name":"7","id":"rs1797856807","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1173891632","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566810,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140566810},{"clinical_significance":[],"id":"rs1466175491","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566811,"feature_type":"variation","strand":1,"end":140566811,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1358027681","clinical_significance":[],"start":140566812,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140566812,"alleles":["T","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1266126401","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140566818,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566818,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1419779706","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566820,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140566820},{"end":140566823,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140566823,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1585648630","seq_region_name":"7","clinical_significance":[]},{"start":140566824,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140566824,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs368157248","clinical_significance":[]},{"start":140566827,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140566827,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs7806874","clinical_significance":[]},{"clinical_significance":[],"id":"rs2130592074","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566828,"feature_type":"variation","strand":1,"end":140566828,"alleles":["T","C"]},{"id":"rs2130592081","seq_region_name":"7","clinical_significance":[],"start":140566831,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140566831,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140566832,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566832,"clinical_significance":[],"seq_region_name":"7","id":"rs1008718772"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566833,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140566833,"clinical_significance":[],"id":"rs1217681400","seq_region_name":"7"},{"start":140566834,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140566834,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1370602672","clinical_significance":[]},{"seq_region_name":"7","id":"rs1018423069","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566843,"source":"dbSNP","strand":1,"feature_type":"variation","end":140566843,"alleles":["A","G"]},{"end":140566844,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140566844,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1797858278","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566846,"feature_type":"variation","strand":1,"end":140566846,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs577608734"},{"end":140566847,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140566847,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs979689149"},{"alleles":["A","C"],"end":140566849,"strand":1,"feature_type":"variation","start":140566849,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs772474472","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797858580","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566851,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140566851},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585648738","end":140566852,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140566852,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140566856,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566856,"source":"dbSNP","seq_region_name":"7","id":"rs1386583752","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1399086692","source":"dbSNP","start":140566857,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140566857,"feature_type":"variation","strand":1},{"alleles":["T","A","G"],"end":140566863,"feature_type":"variation","strand":1,"source":"dbSNP","start":140566863,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1616631","seq_region_name":"7"},{"seq_region_name":"7","id":"rs6951766","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140566864,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566864,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566867,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140566867,"clinical_significance":[],"seq_region_name":"7","id":"rs1797859312"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140566868,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566868,"clinical_significance":[],"seq_region_name":"7","id":"rs1797859428"},{"source":"dbSNP","start":140566869,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140566869,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1174471337"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566873,"source":"dbSNP","strand":1,"feature_type":"variation","end":140566873,"alleles":["C","T"],"seq_region_name":"7","id":"rs1320189489","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140566875,"alleles":["T","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566875,"source":"dbSNP","id":"rs950182827","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1394144523","clinical_significance":[],"end":140566880,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140566880,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs747447837","seq_region_name":"7","end":140566882,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140566882,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1368810484","source":"dbSNP","start":140566885,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140566885,"alleles":["C","G","T"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566887,"feature_type":"variation","strand":1,"end":140566887,"alleles":["G","A"],"clinical_significance":[],"id":"rs1046054378","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566889,"feature_type":"variation","strand":1,"end":140566889,"alleles":["A","G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1450743551"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140566891,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566891,"source":"dbSNP","seq_region_name":"7","id":"rs1204415324","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140566893,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566893,"source":"dbSNP","id":"rs1797860619","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140566896,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140566896,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1797860726","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140566899,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566899,"clinical_significance":[],"seq_region_name":"7","id":"rs1483577401"},{"seq_region_name":"7","id":"rs1221390039","clinical_significance":[],"start":140566900,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140566900,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1299859482","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140566909,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566909},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140566910,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566910,"source":"dbSNP","seq_region_name":"7","id":"rs927533975","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566912,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140566912,"id":"rs1311611336","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1207809277","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140566913,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566913},{"feature_type":"variation","strand":1,"end":140566920,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566920,"clinical_significance":[],"seq_region_name":"7","id":"rs371971852"},{"clinical_significance":[],"seq_region_name":"7","id":"rs937574924","alleles":["C","G","T"],"end":140566923,"feature_type":"variation","strand":1,"source":"dbSNP","start":140566923,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797861619","source":"dbSNP","start":140566925,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140566925,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1797861803","clinical_significance":[],"strand":1,"feature_type":"variation","end":140566929,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566929,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1797861966","seq_region_name":"7","feature_type":"variation","strand":1,"end":140566931,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566931},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566931,"feature_type":"variation","strand":1,"end":140566939,"alleles":["TTTTTTTTT","TTTTTTTT","TTTTTTTTTT"],"clinical_significance":[],"seq_region_name":"7","id":"rs1055212548"},{"alleles":["T","C"],"end":140566936,"strand":1,"feature_type":"variation","start":140566936,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797862376","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566939,"source":"dbSNP","strand":1,"feature_type":"variation","end":140566939,"alleles":["T","A","C"],"seq_region_name":"7","id":"rs1294948371","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566944,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140566944,"id":"rs1397109466","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797863003","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566948,"feature_type":"variation","strand":1,"end":140566948,"alleles":["A","G"]},{"alleles":["A","G"],"end":140566950,"feature_type":"variation","strand":1,"source":"dbSNP","start":140566950,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130592438"},{"source":"dbSNP","start":140566951,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140566951,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1797863160","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566952,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140566952,"id":"rs1797863349","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797863503","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566953,"source":"dbSNP","strand":1,"feature_type":"variation","end":140566953,"alleles":["C","T"]},{"id":"rs1797863690","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566955,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140566955},{"seq_region_name":"7","id":"rs1382028374","clinical_significance":[],"end":140566956,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140566956,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140566959,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566959,"source":"dbSNP","seq_region_name":"7","id":"rs1301432858","clinical_significance":[]},{"id":"rs957138970","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566965,"source":"dbSNP","strand":1,"feature_type":"variation","end":140566965,"alleles":["C","G"]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140566984,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566984,"clinical_significance":[],"id":"rs987843601","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs768987253","feature_type":"variation","strand":1,"end":140566986,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140566986},{"seq_region_name":"7","id":"rs1797864724","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566987,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140566987},{"source":"dbSNP","start":140566990,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140566990,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585649099"},{"source":"dbSNP","start":140566994,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140566994,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797864938"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140566995,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566995,"source":"dbSNP","seq_region_name":"7","id":"rs1797865023","clinical_significance":[]},{"id":"rs917559434","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140566997,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140566997,"source":"dbSNP"},{"alleles":["C","T"],"end":140567001,"strand":1,"feature_type":"variation","start":140567001,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797865230","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797865326","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567009,"source":"dbSNP","strand":1,"feature_type":"variation","end":140567009,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1478902443","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140567013,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567013},{"clinical_significance":[],"seq_region_name":"7","id":"rs375394538","feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140567014,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567014},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567018,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140567018,"clinical_significance":[],"id":"rs578067336","seq_region_name":"7"},{"alleles":["C","A"],"end":140567021,"strand":1,"feature_type":"variation","start":140567021,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797865793","clinical_significance":[]},{"clinical_significance":[],"id":"rs545153746","seq_region_name":"7","end":140567022,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140567022,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs201429061","clinical_significance":[],"strand":1,"feature_type":"variation","end":140567038,"alleles":["GTCCCAACAAGGT","GT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567026,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1159930499","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567028,"feature_type":"variation","strand":1,"end":140567027,"alleles":["-","GATGGTTAGAA"]},{"alleles":["-","TGATGGTTAG"],"end":140567030,"feature_type":"variation","strand":1,"source":"dbSNP","start":140567031,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1377996851"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797866338","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567033,"feature_type":"variation","strand":1,"alleles":["C","-"],"end":140567033},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567036,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140567036,"clinical_significance":[],"seq_region_name":"7","id":"rs1439080215"},{"seq_region_name":"7","id":"rs1797866604","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140567038,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567038,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs545315300","source":"dbSNP","start":140567041,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140567041,"alleles":["T","A","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs768876239","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567043,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140567043},{"id":"rs1797866964","seq_region_name":"7","clinical_significance":[],"alleles":["TT","T"],"end":140567045,"strand":1,"feature_type":"variation","start":140567044,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1229617328","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140567050,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567050,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1258225905","seq_region_name":"7","feature_type":"variation","strand":1,"end":140567051,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567051},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140567054,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567054,"clinical_significance":[],"seq_region_name":"7","id":"rs1585649246"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567054,"source":"dbSNP","strand":1,"feature_type":"variation","end":140567060,"alleles":["GGCAGGC","GGCAGGCAGGC"],"seq_region_name":"7","id":"rs756340091","clinical_significance":[]},{"seq_region_name":"7","id":"rs1330664305","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140567055,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567055,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1202822559","clinical_significance":[],"alleles":["C","T"],"end":140567056,"strand":1,"feature_type":"variation","start":140567056,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1185749582","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567063,"feature_type":"variation","strand":1,"end":140567063,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797867834","alleles":["G","A"],"end":140567065,"feature_type":"variation","strand":1,"source":"dbSNP","start":140567065,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567067,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140567067,"id":"rs1797867940","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs774799025","feature_type":"variation","strand":1,"end":140567069,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567069},{"end":140567070,"alleles":["C","A","G"],"strand":1,"feature_type":"variation","start":140567070,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1451766980","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1200747253","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567071,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140567071},{"clinical_significance":[],"seq_region_name":"7","id":"rs1244695429","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567072,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140567072},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140567074,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567074,"clinical_significance":[],"id":"rs897762477","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567075,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140567075,"seq_region_name":"7","id":"rs1479981744","clinical_significance":[]},{"source":"dbSNP","start":140567077,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140567077,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs73502154"},{"assembly_name":"GRCh38","consequence_type":"splice_region_variant","start":140567077,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CCC","CC"],"end":140567079,"seq_region_name":"7","id":"rs1159885219","clinical_significance":[]},{"start":140567078,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_region_variant","end":140567078,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs372533488","seq_region_name":"7","clinical_significance":["uncertain significance"]},{"consequence_type":"splice_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567079,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140567079,"clinical_significance":[],"seq_region_name":"7","id":"rs773629038"},{"clinical_significance":[],"id":"rs765320743","seq_region_name":"7","alleles":["G","A"],"end":140567081,"feature_type":"variation","strand":1,"source":"dbSNP","start":140567081,"consequence_type":"splice_donor_5th_base_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140567084,"assembly_name":"GRCh38","consequence_type":"splice_donor_variant","start":140567084,"source":"dbSNP","seq_region_name":"7","id":"rs1245665309","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140567086,"assembly_name":"GRCh38","consequence_type":"splice_region_variant","start":140567086,"source":"dbSNP","id":"rs543345285","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140567095,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140567095,"id":"rs752660581","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567098,"feature_type":"variation","strand":1,"end":140567098,"alleles":["C","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1345338299"},{"clinical_significance":[],"seq_region_name":"7","id":"rs758383334","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567117,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140567117},{"start":140567118,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140567118,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs374336112","clinical_significance":["uncertain significance"]},{"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140567119,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140567119,"seq_region_name":"7","id":"rs561524063","clinical_significance":[]},{"seq_region_name":"7","id":"rs1018308296","clinical_significance":[],"start":140567121,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["A","G"],"end":140567121,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1236277208","feature_type":"variation","strand":1,"end":140567122,"alleles":["G","A"],"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567122},{"source":"dbSNP","start":140567123,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140567123,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585649524"},{"seq_region_name":"7","id":"rs1414728924","clinical_significance":[],"alleles":["C","T"],"end":140567127,"strand":1,"feature_type":"variation","start":140567127,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"end":140567129,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140567129,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","id":"rs1259567777","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1356614461","clinical_significance":[],"end":140567130,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140567130,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"source":"dbSNP","start":140567131,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140567131,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs200475620"},{"source":"dbSNP","start":140567133,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140567133,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs780882985","seq_region_name":"7"},{"end":140567134,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140567134,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797871218"},{"start":140567136,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["G","T"],"end":140567136,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797871346","clinical_significance":[]},{"seq_region_name":"7","id":"rs1310314041","clinical_significance":[],"strand":1,"feature_type":"variation","end":140567143,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140567143,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1797871583","clinical_significance":[],"start":140567144,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140567144,"alleles":["T","A","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1490137546","source":"dbSNP","start":140567145,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140567145,"alleles":["G","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1585649619","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","T"],"end":140567151,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567151},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567157,"feature_type":"variation","strand":1,"end":140567157,"alleles":["C","T"],"clinical_significance":[],"id":"rs1797871996","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1182586633","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140567163,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140567163,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140567166,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140567166,"source":"dbSNP","id":"rs1585649645","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs745587244","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140567169,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140567169,"source":"dbSNP"},{"start":140567170,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140567170,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs200641456","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797872718","clinical_significance":[],"start":140567175,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["G","C"],"end":140567175,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs371734352","clinical_significance":["uncertain significance"],"start":140567179,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["C","G"],"end":140567179,"strand":1,"feature_type":"variation"},{"id":"rs202084618","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140567180,"source":"dbSNP","strand":1,"feature_type":"variation","end":140567180,"alleles":["C","T"]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140567186,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140567186,"source":"dbSNP","seq_region_name":"7","id":"rs1473809047","clinical_significance":[]},{"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567188,"feature_type":"variation","strand":1,"end":140567188,"alleles":["G","A"],"clinical_significance":[],"id":"rs1161727121","seq_region_name":"7"},{"source":"dbSNP","start":140567189,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140567189,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs779092613"},{"seq_region_name":"7","id":"rs368995985","clinical_significance":[],"strand":1,"feature_type":"variation","end":140567193,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140567193,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1310181244","clinical_significance":[],"start":140567194,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["G","A","C"],"end":140567194,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs371604238","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140567199,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567199},{"seq_region_name":"7","id":"rs1184139170","clinical_significance":[],"start":140567201,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["T","C"],"end":140567201,"strand":1,"feature_type":"variation"},{"alleles":["C","T"],"end":140567202,"feature_type":"variation","strand":1,"source":"dbSNP","start":140567202,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs773541019"},{"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140567203,"source":"dbSNP","strand":1,"feature_type":"variation","end":140567203,"alleles":["C","T"],"seq_region_name":"7","id":"rs761027420","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140567204,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140567204,"source":"dbSNP","seq_region_name":"7","id":"rs73165431","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs200776468","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567205,"feature_type":"variation","strand":1,"end":140567205,"alleles":["G","A"]},{"clinical_significance":[],"id":"rs762733207","seq_region_name":"7","end":140567212,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140567212,"consequence_type":"synonymous_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140567213,"source":"dbSNP","strand":1,"feature_type":"variation","end":140567213,"alleles":["G","A"],"seq_region_name":"7","id":"rs1797874731","clinical_significance":[]},{"seq_region_name":"7","id":"rs1358231055","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140567215,"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140567215,"source":"dbSNP"},{"clinical_significance":["uncertain significance"],"id":"rs764104594","seq_region_name":"7","alleles":["G","A"],"end":140567216,"feature_type":"variation","strand":1,"source":"dbSNP","start":140567216,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"alleles":["A","T"],"end":140567220,"feature_type":"variation","strand":1,"source":"ClinVar","start":140567220,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":["uncertain significance"],"id":"rs2486171207","seq_region_name":"7"},{"seq_region_name":"7","id":"rs751507436","clinical_significance":[],"start":140567221,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","end":140567221,"alleles":["C","A","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":["uncertain significance"],"seq_region_name":"7","id":"rs761663991","source":"dbSNP","start":140567222,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["C","A","G","T"],"end":140567222,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140567223,"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140567223,"source":"dbSNP","seq_region_name":"7","id":"rs17161631","clinical_significance":[]},{"end":140567224,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140567224,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs755781480"},{"seq_region_name":"7","id":"rs376779332","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140567227,"source":"dbSNP","strand":1,"feature_type":"variation","end":140567227,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs555771873","clinical_significance":[],"end":140567228,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140567228,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"seq_region_name":"7","id":"rs1585649945","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140567232,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140567232,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140567234,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140567234,"source":"dbSNP","id":"rs1797876268","seq_region_name":"7","clinical_significance":[]},{"id":"rs1335576335","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140567237,"source":"dbSNP","strand":1,"feature_type":"variation","end":140567237,"alleles":["A","T"]},{"end":140567238,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140567238,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs980398305","clinical_significance":[]},{"seq_region_name":"7","id":"rs201765157","clinical_significance":[],"strand":1,"feature_type":"variation","end":140567240,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140567240,"source":"dbSNP"},{"id":"rs779473145","seq_region_name":"7","clinical_significance":[],"start":140567241,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["G","A","C"],"end":140567241,"strand":1,"feature_type":"variation"},{"end":140567243,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140567243,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797876968"},{"end":140567246,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140567246,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","id":"rs748647301","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs560474633","consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567248,"feature_type":"variation","strand":1,"end":140567248,"alleles":["C","T"]},{"start":140567250,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["C","T"],"end":140567250,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs772464064","clinical_significance":["uncertain significance"]},{"seq_region_name":"7","id":"rs202162467","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140567251,"source":"dbSNP","strand":1,"feature_type":"variation","end":140567251,"alleles":["G","A"]},{"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140567257,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140567257,"seq_region_name":"7","id":"rs759515264","clinical_significance":[]},{"alleles":["G","A"],"end":140567259,"feature_type":"variation","strand":1,"source":"dbSNP","start":140567259,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs2130593432","seq_region_name":"7"},{"start":140567260,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"inframe_deletion","alleles":["GCGCTGGCTG","G"],"end":140567269,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797877818","clinical_significance":[]},{"seq_region_name":"7","id":"rs375937224","clinical_significance":["uncertain significance"],"start":140567261,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140567261,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":["uncertain significance"],"seq_region_name":"7","id":"rs370243121","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567262,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140567262},{"clinical_significance":["uncertain significance"],"id":"rs759646999","seq_region_name":"7","feature_type":"variation","strand":1,"end":140567264,"alleles":["T","C","G"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567264},{"clinical_significance":[],"seq_region_name":"7","id":"rs1334056471","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567265,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140567265},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567266,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140567266,"clinical_significance":[],"seq_region_name":"7","id":"rs769829758"},{"id":"rs1213368546","seq_region_name":"7","clinical_significance":[],"alleles":["T","A"],"end":140567268,"strand":1,"feature_type":"variation","start":140567268,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"seq_region_name":"7","id":"rs1052116130","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140567269,"source":"dbSNP","strand":1,"feature_type":"variation","end":140567269,"alleles":["G","A"]},{"start":140567271,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["G","A"],"end":140567271,"strand":1,"feature_type":"variation","id":"rs774313413","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","G"],"end":140567272,"strand":1,"feature_type":"variation","start":140567272,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_region_variant","seq_region_name":"7","id":"rs1299347131","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"splice_acceptor_variant","start":140567274,"source":"dbSNP","strand":1,"feature_type":"variation","end":140567274,"alleles":["C","T"],"seq_region_name":"7","id":"rs761705165","clinical_significance":[]},{"seq_region_name":"7","id":"rs1226377713","clinical_significance":[],"start":140567275,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_acceptor_variant","end":140567275,"alleles":["T","A","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs562951654","clinical_significance":[],"start":140567279,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_region_variant","alleles":["T","G"],"end":140567279,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs373668345","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140567280,"assembly_name":"GRCh38","consequence_type":"splice_region_variant","start":140567280,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1585650207","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"splice_region_variant","start":140567281,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140567281},{"start":140567282,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_polypyrimidine_tract_variant","end":140567282,"alleles":["G","T"],"strand":1,"feature_type":"variation","id":"rs1797879809","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140567284,"consequence_type":"splice_polypyrimidine_tract_variant","assembly_name":"GRCh38","end":140567284,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1797879906","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["GAGGGAGAGAGAAAGAGAGAAAGAGAG","GAGGGAGAGAGAAAGAGAGAAAGAGAGGGAGAGAGAAAGAGAGAAAGAGAG"],"end":140567310,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567284,"source":"dbSNP","id":"rs780434748","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797880099","clinical_significance":[],"strand":1,"feature_type":"variation","end":140567285,"alleles":["A","G","T"],"assembly_name":"GRCh38","consequence_type":"splice_polypyrimidine_tract_variant","start":140567285,"source":"dbSNP"},{"end":140567287,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140567287,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_polypyrimidine_tract_variant","id":"rs1199771963","seq_region_name":"7","clinical_significance":[]},{"alleles":["GGAGAGAGAAAGAGAGAA","-"],"end":140567304,"feature_type":"variation","strand":1,"source":"dbSNP","start":140567287,"consequence_type":"splice_polypyrimidine_tract_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1201867981"},{"seq_region_name":"7","id":"rs1435202452","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"splice_polypyrimidine_tract_variant","start":140567288,"source":"dbSNP","strand":1,"feature_type":"variation","end":140567288,"alleles":["G","C"]},{"seq_region_name":"7","id":"rs753903499","clinical_significance":[],"alleles":["GAGAGAGA","GAGA"],"end":140567295,"strand":1,"feature_type":"variation","start":140567288,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797880617","source":"dbSNP","start":140567288,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140567317,"alleles":["GAGAGAGAAAGAGAGAAAGAGAGAGAGAGA","GAGAGAGA"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs199826292","feature_type":"variation","strand":1,"alleles":["AGAGAGAAAGAGAGAAAGAGAGA","AGAGAGA","AGAGAGAAAGAGAGA","AGAGAGAAAGAGAGAAAGAGAGAAAGAGAGA"],"end":140567311,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567289},{"start":140567290,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_polypyrimidine_tract_variant","end":140567290,"alleles":["G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs530387102","clinical_significance":[]},{"seq_region_name":"7","id":"rs760251144","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140567291,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567291,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1797881164","clinical_significance":[],"start":140567291,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140567301,"alleles":["AGAGAAAGAGA","AGAGA"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1563146484","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567291,"source":"dbSNP","strand":1,"feature_type":"variation","end":140567309,"alleles":["AGAGAAAGAGAGAAAGAGA","AGAGA"]},{"alleles":["G","C"],"end":140567292,"feature_type":"variation","strand":1,"source":"dbSNP","start":140567292,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1465716498"},{"feature_type":"variation","strand":1,"end":140567295,"alleles":["AGA","AGATAGA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567293,"clinical_significance":[],"seq_region_name":"7","id":"rs1797881485"},{"feature_type":"variation","strand":1,"alleles":["AGAAAGA","AGA","AGAAAGAAAGA"],"end":140567299,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567293,"clinical_significance":[],"seq_region_name":"7","id":"rs1270529650"},{"alleles":["AGAAAGAGAGAAAGA","AGA"],"end":140567307,"feature_type":"variation","strand":1,"source":"dbSNP","start":140567293,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1322807626"},{"end":140567294,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140567294,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1563146494","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1491433527","end":140567297,"alleles":["AAA","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140567295,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1563146513","clinical_significance":[],"alleles":["AAAGAGAGAAA","A"],"end":140567305,"strand":1,"feature_type":"variation","start":140567295,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567296,"feature_type":"variation","strand":1,"end":140567295,"alleles":["-","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs770694985"},{"seq_region_name":"7","id":"rs946968787","clinical_significance":[],"end":140567296,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","start":140567296,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140567297,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["-","GAG","GG"],"end":140567296,"strand":1,"feature_type":"variation","id":"rs1797882416","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797882553","clinical_significance":[],"start":140567297,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140567297,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1797882650","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567297,"source":"dbSNP","strand":1,"feature_type":"variation","end":140567297,"alleles":["A","AAAGA"]},{"source":"dbSNP","start":140567297,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AGAGAG","AGAGAGGGAGAGAGAGAGAG"],"end":140567302,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797882782"},{"strand":1,"feature_type":"variation","end":140567303,"alleles":["AGAGAGA","A","AGAGA","AGAGAGAGA","AGAGAGAGAGA","AGAGAGAGAGAGA","AGAGAGAGAGAGAGA","AGAGAGAGAGAGAGAGA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567297,"source":"dbSNP","seq_region_name":"7","id":"rs776985629","clinical_significance":[]},{"alleles":["AGAGAGAAAGAGAGAGA","AGAGAGA"],"end":140567313,"feature_type":"variation","strand":1,"source":"dbSNP","start":140567297,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs769390414"},{"id":"rs745664794","seq_region_name":"7","clinical_significance":[],"start":140567297,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AGAGAGAAAGAGAGAGAGA","AGAGAGA"],"end":140567315,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567297,"feature_type":"variation","strand":1,"end":140567317,"alleles":["AGAGAGAAAGAGAGAGAGAGA","AGAGAGA","AGAGAGAAAGAGAGAGAGAGAAAGAGAGAGAGAGA"],"clinical_significance":[],"seq_region_name":"7","id":"rs762497550"},{"alleles":["AGAGAGAAAGAGAGAGAGAGAGA","AGAGAGA"],"end":140567319,"strand":1,"feature_type":"variation","start":140567297,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs775038928","clinical_significance":[]},{"seq_region_name":"7","id":"rs1467757511","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567297,"source":"dbSNP","strand":1,"feature_type":"variation","end":140567321,"alleles":["AGAGAGAAAGAGAGAGAGAGAGAGA","AGAGAGA"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567297,"feature_type":"variation","strand":1,"end":140567323,"alleles":["AGAGAGAAAGAGAGAGAGAGAGAGAGA","AGAGAGA"],"clinical_significance":[],"seq_region_name":"7","id":"rs1393542887"},{"alleles":["AGAGAGAAAGAGAGAGAGAGAGAGAGAGA","AGAGAGA"],"end":140567325,"strand":1,"feature_type":"variation","start":140567297,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1193272332","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["AGAGAGAAAGAGAGAGAGAGAGAGAGAGAGA","AGAGAGA"],"end":140567327,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567297,"clinical_significance":[],"seq_region_name":"7","id":"rs768103611"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567297,"feature_type":"variation","strand":1,"alleles":["AGAGAGAAAGAGAGAGAGAGAGAGAGAGAGAGAGAGA","AGAGAGA"],"end":140567333,"clinical_significance":[],"seq_region_name":"7","id":"rs1797884169"},{"seq_region_name":"7","id":"rs766005494","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140567298,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567298,"source":"dbSNP"},{"id":"rs753503368","seq_region_name":"7","clinical_significance":[],"start":140567299,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140567299,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs200753751","seq_region_name":"7","feature_type":"variation","strand":1,"end":140567309,"alleles":["AGAGAAAGAGA","AGAGA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567299},{"seq_region_name":"7","id":"rs754484704","clinical_significance":[],"start":140567300,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140567300,"alleles":["G","A","C"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["G","-"],"end":140567300,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567300,"source":"dbSNP","seq_region_name":"7","id":"rs1190812957","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797884867","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567301,"source":"dbSNP","strand":1,"feature_type":"variation","end":140567303,"alleles":["AGA","AGACAGA"]},{"alleles":["AGAAAGA","AGA","AGAAAGAAAGA"],"end":140567307,"strand":1,"feature_type":"variation","start":140567301,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs201845097","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797885127","clinical_significance":[],"strand":1,"feature_type":"variation","end":140567302,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567302,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567302,"source":"dbSNP","strand":1,"feature_type":"variation","end":140567308,"alleles":["GAAAGAG","-"],"seq_region_name":"7","id":"rs1259879834","clinical_significance":[]},{"clinical_significance":[],"id":"rs778340182","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567303,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140567303},{"id":"rs1797885472","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","ACA","ATA"],"end":140567303,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567303,"source":"dbSNP"},{"seq_region_name":"7","id":"rs750761053","clinical_significance":[],"start":140567303,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AAA","-"],"end":140567305,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1554470083","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567303,"feature_type":"variation","strand":1,"alleles":["AAA","A","AAAAA"],"end":140567305},{"end":140567303,"alleles":["-","C","G","GAGAG","T"],"strand":1,"feature_type":"variation","start":140567304,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs763966797","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140567304,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567304,"clinical_significance":[],"seq_region_name":"7","id":"rs509440"},{"alleles":["-","G","GAG","GAGAG","GAGAGAG","GAGAGAGAG","GAGAGAGAGAG","GAGAGAGAGAGAG","GAGAGAGAGAGAGAG"],"end":140567304,"strand":1,"feature_type":"variation","start":140567305,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1554470084","clinical_significance":[]},{"end":140567305,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140567305,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs753199446"},{"seq_region_name":"7","id":"rs1797886608","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567305,"source":"dbSNP","strand":1,"feature_type":"variation","end":140567311,"alleles":["AGAGAGA","AGAGAGAAAGAGAGAGAGA"]},{"seq_region_name":"7","id":"rs60964847","clinical_significance":[],"start":140567305,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140567345,"alleles":["AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA","AGAGAGAGAGAGAGAGAGAGA","AGAGAGAGAGAGAGAGAGAGAGA","AGAGAGAGAGAGAGAGAGAGAGAGA","AGAGAGAGAGAGAGAGAGAGAGAGAGA","AGAGAGAGAGAGAGAGAGAGAGAGAGAGA","AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA","AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA","AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA","AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA","AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA","AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA","AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA","AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA","AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA","AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA","AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA","AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA","AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA","AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA","AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA","AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA","AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA","AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA","AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567306,"feature_type":"variation","strand":1,"end":140567306,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1000877777"},{"id":"rs781118595","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567307,"source":"dbSNP","strand":1,"feature_type":"variation","end":140567307,"alleles":["A","-"]},{"seq_region_name":"7","id":"rs1032496244","clinical_significance":[],"start":140567307,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140567307,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"id":"rs1797887766","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567307,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","AAA","ACA"],"end":140567307},{"end":140567309,"alleles":["AGA","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140567307,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs745624321","seq_region_name":"7"},{"alleles":["AGAG","AGAGGGAGAGAGAAAGAGAGAAAGAG"],"end":140567310,"strand":1,"feature_type":"variation","start":140567307,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797888097","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs779737670","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567307,"feature_type":"variation","strand":1,"alleles":["AGAGA","-"],"end":140567311},{"clinical_significance":[],"seq_region_name":"7","id":"rs769620161","feature_type":"variation","strand":1,"alleles":["AGAGAGA","-"],"end":140567313,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567307},{"seq_region_name":"7","id":"rs868710707","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567308,"source":"dbSNP","strand":1,"feature_type":"variation","end":140567308,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1797888564","clinical_significance":[],"strand":1,"feature_type":"variation","end":140567309,"alleles":["A","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567309,"source":"dbSNP"},{"id":"rs892624181","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567310,"source":"dbSNP","strand":1,"feature_type":"variation","end":140567310,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1379894473","clinical_significance":[],"alleles":["G","-"],"end":140567310,"strand":1,"feature_type":"variation","start":140567310,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1274475197","seq_region_name":"7","source":"dbSNP","start":140567310,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["GAGAG","-"],"end":140567314,"feature_type":"variation","strand":1},{"start":140567311,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140567311,"strand":1,"feature_type":"variation","id":"rs1009855136","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797889057","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567311,"feature_type":"variation","strand":1,"end":140567311,"alleles":["A","AAA"]},{"seq_region_name":"7","id":"rs1212336501","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567311,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AGAGAGA","AGAGAGACAGAGAGA"],"end":140567317},{"start":140567312,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140567312,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs1025655437","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1263687252","end":140567314,"alleles":["GAG","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140567312,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140567314,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140567314,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs970962411","clinical_significance":[]},{"seq_region_name":"7","id":"rs1353256140","clinical_significance":[],"strand":1,"feature_type":"variation","end":140567315,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567315,"source":"dbSNP"},{"seq_region_name":"7","id":"rs759005641","clinical_significance":[],"alleles":["G","A"],"end":140567316,"strand":1,"feature_type":"variation","start":140567316,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1435164811","source":"dbSNP","start":140567316,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140567318,"alleles":["GAG","GAGGGAG"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797889943","source":"dbSNP","start":140567317,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140567317,"alleles":["A","G"],"feature_type":"variation","strand":1},{"id":"rs1359376178","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567318,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140567318},{"end":140567319,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140567319,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797890198"},{"alleles":["G","A","C"],"end":140567320,"strand":1,"feature_type":"variation","start":140567320,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs778218804","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140567321,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567321,"clinical_significance":[],"id":"rs1797890419","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1301642276","clinical_significance":[],"end":140567322,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140567322,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1313886146","seq_region_name":"7","end":140567324,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140567324,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1409403144","alleles":["A","T"],"end":140567325,"feature_type":"variation","strand":1,"source":"dbSNP","start":140567325,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1797890740","clinical_significance":[],"alleles":["G","A"],"end":140567326,"strand":1,"feature_type":"variation","start":140567326,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["-","GC"],"end":140567326,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567327,"clinical_significance":[],"id":"rs1797890847","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140567328,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567328,"source":"dbSNP","seq_region_name":"7","id":"rs1033315183","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585650973","clinical_significance":[],"alleles":["G","C","T"],"end":140567330,"strand":1,"feature_type":"variation","start":140567330,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567332,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140567332,"seq_region_name":"7","id":"rs963151248","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567334,"source":"dbSNP","strand":1,"feature_type":"variation","end":140567334,"alleles":["G","C"],"seq_region_name":"7","id":"rs1417579531","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567336,"feature_type":"variation","strand":1,"end":140567336,"alleles":["G","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs973133283"},{"end":140567337,"alleles":["A","ACA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140567337,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797891547"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567337,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AGAGAGAGACAGAG","AGAG"],"end":140567350,"seq_region_name":"7","id":"rs1797891644","clinical_significance":[]},{"seq_region_name":"7","id":"rs1483163262","clinical_significance":[],"end":140567338,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140567338,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797891832","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567339,"feature_type":"variation","strand":1,"end":140567339,"alleles":["A","G"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567340,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140567340,"id":"rs548562098","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140567340,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140567340,"alleles":["G","GGG"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797892063"},{"alleles":["AGAGA","AGAGAGACAGAGA"],"end":140567345,"feature_type":"variation","strand":1,"source":"dbSNP","start":140567341,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1445904935"},{"id":"rs1289973753","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567341,"source":"dbSNP","strand":1,"feature_type":"variation","end":140567350,"alleles":["AGAGACAGAG","AGAG","AGAGACAGAGACAGAG"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567342,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140567342,"clinical_significance":[],"seq_region_name":"7","id":"rs1235052813"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567343,"source":"dbSNP","strand":1,"feature_type":"variation","end":140567343,"alleles":["A","G"],"id":"rs1797892550","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1797892653","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["AGA","AGAGAGACAGA","AGAGAGAGAGAGAGACAGA"],"end":140567345,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567343},{"seq_region_name":"7","id":"rs1797892784","clinical_significance":[],"start":140567343,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140567349,"alleles":["AGACAGA","AGA"],"strand":1,"feature_type":"variation"},{"alleles":["G","C"],"end":140567344,"feature_type":"variation","strand":1,"source":"dbSNP","start":140567344,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs929126218"},{"seq_region_name":"7","id":"rs35481576","clinical_significance":[],"alleles":["A","C"],"end":140567345,"strand":1,"feature_type":"variation","start":140567345,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1797893144","clinical_significance":[],"start":140567345,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140567347,"alleles":["ACA","A","ACACA"],"strand":1,"feature_type":"variation"},{"id":"rs987289705","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567346,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140567346},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567347,"feature_type":"variation","strand":1,"end":140567347,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1375297523"},{"source":"dbSNP","start":140567347,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AGAG","AG"],"end":140567350,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797893408"},{"alleles":["G","C"],"end":140567348,"feature_type":"variation","strand":1,"source":"dbSNP","start":140567348,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797893505"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567351,"feature_type":"variation","strand":1,"end":140567351,"alleles":["T","A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs902543534"},{"start":140567351,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140567357,"alleles":["TGAGCAA","-"],"strand":1,"feature_type":"variation","id":"rs1256084021","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1797893851","seq_region_name":"7","alleles":["C","-"],"end":140567355,"feature_type":"variation","strand":1,"source":"dbSNP","start":140567355,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140567356,"alleles":["CA","-"],"strand":1,"feature_type":"variation","start":140567355,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797893949","clinical_significance":[]},{"end":140567357,"alleles":["CAA","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140567355,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797894032"},{"start":140567358,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140567357,"alleles":["-","GAG","GAGAG","GAGAGAG"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797894129","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs911801631","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567370,"feature_type":"variation","strand":1,"end":140567370,"alleles":["G","A","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs567267346","end":140567373,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140567373,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797894596","source":"dbSNP","start":140567374,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140567374,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140567375,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567375,"clinical_significance":[],"seq_region_name":"7","id":"rs534590335"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1238741103","alleles":["C","T"],"end":140567380,"feature_type":"variation","strand":1,"source":"dbSNP","start":140567380,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1797894938","clinical_significance":[],"start":140567382,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140567382,"strand":1,"feature_type":"variation"},{"id":"rs544697216","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567388,"source":"dbSNP","strand":1,"feature_type":"variation","end":140567406,"alleles":["AATTGTGCCGAGCTGCAAT","AAT"]},{"end":140567390,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140567390,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797895209","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567393,"source":"dbSNP","strand":1,"feature_type":"variation","end":140567393,"alleles":["T","C","G"],"id":"rs1394450680","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs943266271","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567396,"feature_type":"variation","strand":1,"end":140567396,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs546805557","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567397,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140567397},{"end":140567406,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140567406,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs571318369","clinical_significance":[]},{"seq_region_name":"7","id":"rs1175047745","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567408,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GG","G"],"end":140567409},{"start":140567411,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140567411,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs188944479","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567412,"source":"dbSNP","strand":1,"feature_type":"variation","end":140567412,"alleles":["A","G"],"id":"rs1246767309","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140567413,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140567413,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs114263117","seq_region_name":"7"},{"id":"rs1797913417","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567415,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140567415},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797913575","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567420,"feature_type":"variation","strand":1,"end":140567420,"alleles":["A","C","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs892517345","feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140567421,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567421},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567422,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140567422,"clinical_significance":[],"id":"rs1272430698","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567428,"source":"dbSNP","strand":1,"feature_type":"variation","end":140567428,"alleles":["A","G"],"seq_region_name":"7","id":"rs1409961539","clinical_significance":[]},{"seq_region_name":"7","id":"rs753487423","clinical_significance":[],"alleles":["A","G"],"end":140567429,"strand":1,"feature_type":"variation","start":140567429,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140567430,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140567430,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797914159"},{"clinical_significance":[],"id":"rs1797914283","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140567432,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567432},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567434,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140567434,"seq_region_name":"7","id":"rs76284493","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1342395127","feature_type":"variation","strand":1,"end":140567439,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567439},{"clinical_significance":[],"seq_region_name":"7","id":"rs1446033746","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140567440,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567440},{"clinical_significance":[],"id":"rs1797914795","seq_region_name":"7","source":"dbSNP","start":140567444,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140567444,"alleles":["T","C"],"feature_type":"variation","strand":1},{"id":"rs893159892","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567447,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140567447},{"start":140567448,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140567448,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1223420663","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130594864","alleles":["G","A"],"end":140567454,"feature_type":"variation","strand":1,"source":"dbSNP","start":140567454,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1797915124","clinical_significance":[],"end":140567455,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140567455,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs2130594884","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567457,"source":"dbSNP","strand":1,"feature_type":"variation","end":140567457,"alleles":["T","G"]},{"seq_region_name":"7","id":"rs1292945312","clinical_significance":[],"start":140567459,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140567459,"alleles":["T","-"],"strand":1,"feature_type":"variation"},{"id":"rs1797915243","seq_region_name":"7","clinical_significance":[],"alleles":["T","G"],"end":140567459,"strand":1,"feature_type":"variation","start":140567459,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1368637817","source":"dbSNP","start":140567460,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140567460,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567461,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140567461,"clinical_significance":[],"seq_region_name":"7","id":"rs1305685277"},{"id":"rs1438758063","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567463,"source":"dbSNP","strand":1,"feature_type":"variation","end":140567463,"alleles":["T","A"]},{"feature_type":"variation","strand":1,"end":140567470,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567470,"clinical_significance":[],"seq_region_name":"7","id":"rs1585651389"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567471,"feature_type":"variation","strand":1,"end":140567471,"alleles":["A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1797915825"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1370374573","end":140567473,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140567473,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1321737516","feature_type":"variation","strand":1,"end":140567475,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567475},{"strand":1,"feature_type":"variation","end":140567482,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567482,"source":"dbSNP","seq_region_name":"7","id":"rs1797916158","clinical_significance":[]},{"seq_region_name":"7","id":"rs1455805961","clinical_significance":[],"start":140567484,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140567488,"alleles":["TCTTT","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1797916411","clinical_significance":[],"end":140567488,"alleles":["TTT","T"],"strand":1,"feature_type":"variation","start":140567486,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797916523","end":140567489,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140567489,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["G","T"],"end":140567493,"feature_type":"variation","strand":1,"source":"dbSNP","start":140567493,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1343797598"},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140567498,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567498,"source":"dbSNP","seq_region_name":"7","id":"rs1797916756","clinical_significance":[]},{"alleles":["C","A"],"end":140567511,"feature_type":"variation","strand":1,"source":"dbSNP","start":140567511,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797916873"},{"source":"dbSNP","start":140567513,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140567513,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1010244906"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567514,"source":"dbSNP","strand":1,"feature_type":"variation","end":140567514,"alleles":["G","A"],"seq_region_name":"7","id":"rs1399732562","clinical_significance":[]},{"start":140567520,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140567520,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs536692544","clinical_significance":[]},{"seq_region_name":"7","id":"rs1340827095","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140567521,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567521,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797917521","alleles":["T","C"],"end":140567531,"feature_type":"variation","strand":1,"source":"dbSNP","start":140567531,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["T","A"],"end":140567532,"strand":1,"feature_type":"variation","start":140567532,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs554981188","clinical_significance":[]},{"clinical_significance":[],"id":"rs1251840655","seq_region_name":"7","source":"dbSNP","start":140567538,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140567538,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1797917879","clinical_significance":[],"strand":1,"feature_type":"variation","end":140567539,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567539,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs906790900","alleles":["A","G"],"end":140567541,"feature_type":"variation","strand":1,"source":"dbSNP","start":140567541,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797918083","source":"dbSNP","start":140567550,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140567550,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140567554,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567554,"clinical_significance":[],"id":"rs1797918210","seq_region_name":"7"},{"start":140567562,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140567562,"alleles":["C","G"],"strand":1,"feature_type":"variation","id":"rs1486841583","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1258717998","clinical_significance":[],"start":140567571,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140567571,"strand":1,"feature_type":"variation"},{"end":140567572,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140567572,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1002441924","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1214861549","clinical_significance":[],"end":140567578,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140567578,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1797918664","clinical_significance":[],"strand":1,"feature_type":"variation","end":140567579,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567579,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1797918789","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567580,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140567580},{"source":"dbSNP","start":140567588,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140567588,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1312593229"},{"strand":1,"feature_type":"variation","end":140567589,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567589,"source":"dbSNP","seq_region_name":"7","id":"rs1033370924","clinical_significance":[]},{"source":"dbSNP","start":140567590,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140567590,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130595145"},{"seq_region_name":"7","id":"rs1232383092","clinical_significance":[],"alleles":["T","C","G"],"end":140567592,"strand":1,"feature_type":"variation","start":140567592,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1298511890","source":"dbSNP","start":140567597,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140567597,"alleles":["T","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1338665362","clinical_significance":[],"end":140567600,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140567600,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs963038589","seq_region_name":"7","feature_type":"variation","strand":1,"end":140567608,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567608},{"clinical_significance":[],"id":"rs573516400","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140567609,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567609},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567621,"feature_type":"variation","strand":1,"end":140567621,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1563146873"},{"id":"rs1360552525","seq_region_name":"7","clinical_significance":[],"end":140567625,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140567625,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["T","C"],"end":140567630,"strand":1,"feature_type":"variation","start":140567630,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797920095","clinical_significance":[]},{"id":"rs1797920212","seq_region_name":"7","clinical_significance":[],"start":140567633,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140567633,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1026493081","clinical_significance":[],"end":140567637,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140567637,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140567639,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567639,"clinical_significance":[],"id":"rs1449159039","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140567644,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567644,"clinical_significance":[],"seq_region_name":"7","id":"rs1797920576"},{"clinical_significance":[],"id":"rs369823393","seq_region_name":"7","source":"dbSNP","start":140567645,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140567645,"alleles":["G","A"],"feature_type":"variation","strand":1},{"alleles":["G","A","T"],"end":140567646,"feature_type":"variation","strand":1,"source":"dbSNP","start":140567646,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1563146895","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140567650,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567650,"clinical_significance":[],"id":"rs1034543756","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1585651653","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140567651,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567651,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1175056004","source":"dbSNP","start":140567652,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140567652,"alleles":["G","C"],"feature_type":"variation","strand":1},{"id":"rs1585651673","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140567655,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567655,"source":"dbSNP"},{"id":"rs1432551028","seq_region_name":"7","clinical_significance":[],"alleles":["T","A"],"end":140567657,"strand":1,"feature_type":"variation","start":140567657,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1393940907","clinical_significance":[],"end":140567658,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140567658,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140567661,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140567661,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1170591754","clinical_significance":[]},{"id":"rs958891798","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140567662,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567662,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1585651734","seq_region_name":"7","feature_type":"variation","strand":1,"end":140567664,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567664},{"source":"dbSNP","start":140567668,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140567668,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs540537316"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140567669,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567669,"source":"dbSNP","seq_region_name":"7","id":"rs909465849","clinical_significance":[]},{"seq_region_name":"7","id":"rs940898526","clinical_significance":[],"start":140567673,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140567673,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1797922742","clinical_significance":[],"strand":1,"feature_type":"variation","end":140567677,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567677,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140567679,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567679,"source":"dbSNP","id":"rs987729236","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs911700909","source":"dbSNP","start":140567680,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140567680,"alleles":["G","A","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1797923189","seq_region_name":"7","end":140567684,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140567684,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["G","T"],"end":140567687,"strand":1,"feature_type":"variation","start":140567687,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130595405","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140567691,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567691,"source":"dbSNP","id":"rs1797923304","seq_region_name":"7","clinical_significance":[]},{"end":140567698,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140567698,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs565498740","clinical_significance":[]},{"id":"rs577321276","seq_region_name":"7","clinical_significance":[],"start":140567706,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140567706,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1797923684","clinical_significance":[],"end":140567712,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140567712,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1305870545","clinical_significance":[],"alleles":["G","A"],"end":140567720,"strand":1,"feature_type":"variation","start":140567720,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1050782859","feature_type":"variation","strand":1,"end":140567726,"alleles":["TTTT","TTT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567723},{"seq_region_name":"7","id":"rs2130595473","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140567724,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567724,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1404397698","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567732,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140567732},{"start":140567733,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140567733,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797924139","clinical_significance":[]},{"source":"dbSNP","start":140567738,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140567738,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs921297750"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567741,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140567741,"clinical_significance":[],"seq_region_name":"7","id":"rs1311503652"},{"feature_type":"variation","strand":1,"end":140567756,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567756,"clinical_significance":[],"seq_region_name":"7","id":"rs796777122"},{"seq_region_name":"7","id":"rs1797924635","clinical_significance":[],"start":140567759,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140567759,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1412839821","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140567762,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567762,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1374514321","seq_region_name":"7","alleles":["A","G"],"end":140567763,"feature_type":"variation","strand":1,"source":"dbSNP","start":140567763,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140567765,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567765,"clinical_significance":[],"seq_region_name":"7","id":"rs1298420863"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567776,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140567776,"clinical_significance":[],"seq_region_name":"7","id":"rs1797925088"},{"end":140567779,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140567779,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs936682894"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797925312","source":"dbSNP","start":140567781,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140567781,"alleles":["A","G"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140567788,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567788,"clinical_significance":[],"seq_region_name":"7","id":"rs1053753628"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585651910","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567790,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140567790},{"seq_region_name":"7","id":"rs544716586","clinical_significance":[],"end":140567793,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140567793,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140567797,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140567797,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1361395848","clinical_significance":[]},{"seq_region_name":"7","id":"rs1418275433","clinical_significance":[],"alleles":["C","T"],"end":140567799,"strand":1,"feature_type":"variation","start":140567799,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1003470610","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567800,"feature_type":"variation","strand":1,"end":140567800,"alleles":["A","C"]},{"clinical_significance":[],"id":"rs1585651959","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567803,"feature_type":"variation","strand":1,"end":140567803,"alleles":["T","C"]},{"feature_type":"variation","strand":1,"end":140567805,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567805,"clinical_significance":[],"seq_region_name":"7","id":"rs1370853361"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567806,"source":"dbSNP","strand":1,"feature_type":"variation","end":140567806,"alleles":["C","T"],"seq_region_name":"7","id":"rs1797926349","clinical_significance":[]},{"alleles":["T","A","C"],"end":140567808,"strand":1,"feature_type":"variation","start":140567808,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1261375233","clinical_significance":[]},{"clinical_significance":[],"id":"rs1402156735","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140567812,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567812},{"start":140567813,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140567813,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1475534779","clinical_significance":[]},{"clinical_significance":[],"id":"rs1797926758","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140567814,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567814},{"end":140567816,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140567816,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1797926865","seq_region_name":"7","clinical_significance":[]},{"alleles":["CTCT","CT"],"end":140567823,"strand":1,"feature_type":"variation","start":140567820,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797926971","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140567824,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567824,"clinical_significance":[],"seq_region_name":"7","id":"rs942540505"},{"end":140567825,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140567825,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1276042074"},{"start":140567827,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140567827,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797927337","clinical_significance":[]},{"seq_region_name":"7","id":"rs1185596211","clinical_significance":[],"strand":1,"feature_type":"variation","end":140567828,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567828,"source":"dbSNP"},{"id":"rs1797927561","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140567832,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567832,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1325661691","seq_region_name":"7","source":"dbSNP","start":140567835,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140567835,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567836,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140567836,"id":"rs1485450868","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs116668894","clinical_significance":[],"end":140567838,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140567838,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140567839,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140567839,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1462851778"},{"seq_region_name":"7","id":"rs1797928157","clinical_significance":[],"start":140567841,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140567841,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1197801180","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140567843,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567843,"source":"dbSNP"},{"alleles":["A","G"],"end":140567845,"feature_type":"variation","strand":1,"source":"dbSNP","start":140567845,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1276550350"},{"source":"dbSNP","start":140567852,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140567852,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797928485"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797928579","source":"dbSNP","start":140567856,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140567856,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140567859,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567859,"clinical_significance":[],"seq_region_name":"7","id":"rs1479666025"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140567860,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567860,"source":"dbSNP","id":"rs533235180","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1010128745","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567861,"feature_type":"variation","strand":1,"end":140567861,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1047028230","source":"dbSNP","start":140567862,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140567862,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs906680109","feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140567864,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567864},{"clinical_significance":[],"seq_region_name":"7","id":"rs1291785479","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567866,"feature_type":"variation","strand":1,"end":140567866,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1233010644","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567867,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140567867},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797929509","alleles":["T","C"],"end":140567875,"feature_type":"variation","strand":1,"source":"dbSNP","start":140567875,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797929634","source":"dbSNP","start":140567876,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140567876,"alleles":["G","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1797929763","clinical_significance":[],"start":140567879,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140567879,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1351508238","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567882,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140567882},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130595874","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567884,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140567884},{"clinical_significance":[],"seq_region_name":"7","id":"rs778432726","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567885,"feature_type":"variation","strand":1,"end":140567885,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1307189070","source":"dbSNP","start":140567887,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140567887,"feature_type":"variation","strand":1},{"start":140567888,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140567888,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs545224359","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140567910,"alleles":["GGGTCACTGAGTGGAC","GGGTCACTGAGTGGACGGGTCACTGAGTGGAC"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567895,"source":"dbSNP","seq_region_name":"7","id":"rs1797930313","clinical_significance":[]},{"alleles":["G","C"],"end":140567896,"feature_type":"variation","strand":1,"source":"dbSNP","start":140567896,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs745377648"},{"start":140567903,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140567903,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1393692238","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1297164561","end":140567912,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140567912,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140567913,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567913,"clinical_significance":[],"seq_region_name":"7","id":"rs1797930792"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797930935","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140567914,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567914},{"clinical_significance":[],"seq_region_name":"7","id":"rs1055378651","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567915,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140567915},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140567916,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567916,"source":"dbSNP","seq_region_name":"7","id":"rs1797931196","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797931307","source":"dbSNP","start":140567921,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140567921,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1214064201","alleles":["C","T"],"end":140567926,"feature_type":"variation","strand":1,"source":"dbSNP","start":140567926,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140567927,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140567927,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs192159502","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140567933,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567933,"clinical_significance":[],"id":"rs1797931651","seq_region_name":"7"},{"start":140567937,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140567937,"alleles":["C","A","G"],"strand":1,"feature_type":"variation","id":"rs994510058","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797931908","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567940,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140567940},{"id":"rs1025957538","seq_region_name":"7","clinical_significance":[],"start":140567945,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C"],"end":140567945,"strand":1,"feature_type":"variation"},{"start":140567947,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140567947,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797932161","clinical_significance":[]},{"source":"dbSNP","start":140567948,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140567948,"alleles":["T","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1200121839","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567951,"feature_type":"variation","strand":1,"end":140567951,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs184897413"},{"alleles":["TTTTTTTT","TTTTTTT","TTTTTTTTT"],"end":140567958,"feature_type":"variation","strand":1,"source":"dbSNP","start":140567951,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1379894500","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1797932684","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567953,"source":"dbSNP","strand":1,"feature_type":"variation","end":140567953,"alleles":["T","G"]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140567955,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567955,"clinical_significance":[],"seq_region_name":"7","id":"rs1563147148"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567957,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140567957,"seq_region_name":"7","id":"rs1797932888","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567961,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140567961,"clinical_significance":[],"seq_region_name":"7","id":"rs1797933004"},{"strand":1,"feature_type":"variation","end":140567962,"alleles":["A","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567962,"source":"dbSNP","seq_region_name":"7","id":"rs1184169672","clinical_significance":[]},{"id":"rs1797933240","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140567963,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567963,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1417617300","alleles":["A","AA"],"end":140567964,"feature_type":"variation","strand":1,"source":"dbSNP","start":140567964,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797933434","alleles":["G","C"],"end":140567965,"feature_type":"variation","strand":1,"source":"dbSNP","start":140567965,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140567967,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140567967,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1249882494","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797933631","feature_type":"variation","strand":1,"end":140567968,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567968},{"seq_region_name":"7","id":"rs1797933732","clinical_significance":[],"alleles":["A","G"],"end":140567972,"strand":1,"feature_type":"variation","start":140567972,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs950533675","seq_region_name":"7","clinical_significance":[],"end":140567973,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140567973,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1797933953","clinical_significance":[],"end":140567976,"alleles":["CTCT","CT"],"strand":1,"feature_type":"variation","start":140567973,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140567976,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140567976,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797934091"},{"seq_region_name":"7","id":"rs189613369","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140567980,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567980,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1019218404","source":"dbSNP","start":140567981,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140567981,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797934424","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567983,"feature_type":"variation","strand":1,"end":140567983,"alleles":["C","T"]},{"alleles":["A","G"],"end":140567984,"feature_type":"variation","strand":1,"source":"dbSNP","start":140567984,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs528400468"},{"end":140567985,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140567985,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797934653"},{"start":140567987,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140567987,"alleles":["C","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1006390124","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797934871","feature_type":"variation","strand":1,"end":140567988,"alleles":["T","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567988},{"end":140567990,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140567990,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797934972"},{"seq_region_name":"7","id":"rs1016809333","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140567992,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140567992},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797935217","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140567994,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567994},{"alleles":["C","T"],"end":140567995,"strand":1,"feature_type":"variation","start":140567995,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1351762478","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567996,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140567996,"clinical_significance":[],"seq_region_name":"7","id":"rs1797935421"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1262941007","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140567998,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140567998},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568001,"feature_type":"variation","strand":1,"end":140568001,"alleles":["C","T"],"clinical_significance":[],"id":"rs1240734521","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140568002,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568002,"source":"dbSNP","seq_region_name":"7","id":"rs758973204","clinical_significance":[]},{"clinical_significance":[],"id":"rs962280239","seq_region_name":"7","alleles":["A","G"],"end":140568005,"feature_type":"variation","strand":1,"source":"dbSNP","start":140568005,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568018,"feature_type":"variation","strand":1,"end":140568018,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1797936036"},{"seq_region_name":"7","id":"rs974513954","clinical_significance":[],"start":140568019,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140568019,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1585652456","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568021,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140568021},{"clinical_significance":[],"seq_region_name":"7","id":"rs1440956020","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140568026,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568026},{"clinical_significance":[],"seq_region_name":"7","id":"rs972263709","end":140568027,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140568027,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs925874759","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568029,"feature_type":"variation","strand":1,"end":140568029,"alleles":["C","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568030,"source":"dbSNP","strand":1,"feature_type":"variation","end":140568030,"alleles":["T","C"],"seq_region_name":"7","id":"rs1387149345","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797936788","source":"dbSNP","start":140568032,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140568032,"alleles":["C","A"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568033,"feature_type":"variation","strand":1,"end":140568033,"alleles":["C","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs957258978"},{"clinical_significance":[],"seq_region_name":"7","id":"rs989897594","end":140568034,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140568034,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs918276432","feature_type":"variation","strand":1,"end":140568039,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568039},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797937353","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568040,"feature_type":"variation","strand":1,"end":140568040,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs1797937460","clinical_significance":[],"end":140568042,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140568042,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1194525818","seq_region_name":"7","clinical_significance":[],"end":140568043,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140568043,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140568047,"alleles":["A","C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140568047,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1455596995"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568048,"source":"dbSNP","strand":1,"feature_type":"variation","end":140568048,"alleles":["C","T"],"seq_region_name":"7","id":"rs1797937856","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568049,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140568049,"seq_region_name":"7","id":"rs1797937958","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797938070","clinical_significance":[],"end":140568050,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140568050,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140568051,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140568051,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs546548847"},{"end":140568053,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140568053,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs560309955"},{"source":"dbSNP","start":140568054,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140568054,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1193548774"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140568055,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568055,"source":"dbSNP","seq_region_name":"7","id":"rs1329266034","clinical_significance":[]},{"seq_region_name":"7","id":"rs913889150","clinical_significance":[],"alleles":["C","A","T"],"end":140568060,"strand":1,"feature_type":"variation","start":140568060,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140568061,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140568061,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1797938755","seq_region_name":"7"},{"clinical_significance":[],"id":"rs955028272","seq_region_name":"7","alleles":["G","A"],"end":140568066,"feature_type":"variation","strand":1,"source":"dbSNP","start":140568066,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1233524180","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140568068,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568068},{"seq_region_name":"7","id":"rs1309322510","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568069,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140568069},{"clinical_significance":[],"seq_region_name":"7","id":"rs1355260254","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140568072,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568072},{"source":"dbSNP","start":140568073,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140568073,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797939333"},{"seq_region_name":"7","id":"rs1563147274","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568077,"source":"dbSNP","strand":1,"feature_type":"variation","end":140568077,"alleles":["A","G"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568078,"source":"dbSNP","strand":1,"feature_type":"variation","end":140568079,"alleles":["TT","T"],"id":"rs767485541","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568082,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140568082,"clinical_significance":[],"id":"rs1284809003","seq_region_name":"7"},{"start":140568085,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","T"],"end":140568085,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs945474965","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1237461962","feature_type":"variation","strand":1,"end":140568086,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568086},{"source":"dbSNP","start":140568087,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140568087,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs986546115"},{"id":"rs1797940186","seq_region_name":"7","clinical_significance":[],"end":140568094,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140568094,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568095,"feature_type":"variation","strand":1,"end":140568095,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585652716"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568098,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140568098,"seq_region_name":"7","id":"rs2130596489","clinical_significance":[]},{"end":140568099,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140568099,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1797940407","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568106,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140568106,"clinical_significance":[],"seq_region_name":"7","id":"rs1797940505"},{"start":140568108,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140568108,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1563147301","clinical_significance":[]},{"clinical_significance":[],"id":"rs1046475038","seq_region_name":"7","alleles":["A","G"],"end":140568114,"feature_type":"variation","strand":1,"source":"dbSNP","start":140568114,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568115,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140568115,"seq_region_name":"7","id":"rs1797940873","clinical_significance":[]},{"clinical_significance":[],"id":"rs571421212","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568116,"feature_type":"variation","strand":1,"end":140568116,"alleles":["A","G"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568126,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140568126,"clinical_significance":[],"seq_region_name":"7","id":"rs1326994396"},{"clinical_significance":[],"seq_region_name":"7","id":"rs928154196","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568130,"feature_type":"variation","strand":1,"end":140568130,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797949867","source":"dbSNP","start":140568131,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140568131,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568134,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140568134,"seq_region_name":"7","id":"rs1384091504","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140568139,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568139,"source":"dbSNP","id":"rs910970398","seq_region_name":"7","clinical_significance":[]},{"start":140568140,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140568140,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs538797661","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568147,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140568147,"clinical_significance":[],"seq_region_name":"7","id":"rs1436885504"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568149,"feature_type":"variation","strand":1,"end":140568149,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1797950461"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1393337187","source":"dbSNP","start":140568152,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140568152,"alleles":["G","A"],"feature_type":"variation","strand":1},{"alleles":["C","T"],"end":140568154,"feature_type":"variation","strand":1,"source":"dbSNP","start":140568154,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1210796195","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1173151838","clinical_significance":[],"alleles":["G","A"],"end":140568156,"strand":1,"feature_type":"variation","start":140568156,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568157,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140568157,"seq_region_name":"7","id":"rs1476010941","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140568158,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568158,"clinical_significance":[],"seq_region_name":"7","id":"rs1244298695"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797951143","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568164,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140568164},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140568165,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568165,"source":"dbSNP","id":"rs1191695218","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs180822717","seq_region_name":"7","source":"dbSNP","start":140568169,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140568169,"alleles":["C","A","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs527569080","clinical_significance":[],"start":140568170,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140568170,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568171,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140568171,"clinical_significance":[],"id":"rs569402848","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568173,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140568173,"clinical_significance":[],"seq_region_name":"7","id":"rs995071686"},{"seq_region_name":"7","id":"rs1238824157","clinical_significance":[],"strand":1,"feature_type":"variation","end":140568177,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568177,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797952003","alleles":["G","C"],"end":140568178,"feature_type":"variation","strand":1,"source":"dbSNP","start":140568178,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1211153735","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140568180,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568180,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs914366316","source":"dbSNP","start":140568181,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140568181,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1441628238","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568182,"feature_type":"variation","strand":1,"end":140568182,"alleles":["C","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568183,"feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140568183,"clinical_significance":[],"id":"rs1585652936","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1797952640","clinical_significance":[],"start":140568185,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140568185,"strand":1,"feature_type":"variation"},{"id":"rs377148802","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568186,"source":"dbSNP","strand":1,"feature_type":"variation","end":140568186,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs750725579","clinical_significance":[],"start":140568187,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140568187,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"end":140568191,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140568191,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1363421303"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1225155927","alleles":["G","A"],"end":140568192,"feature_type":"variation","strand":1,"source":"dbSNP","start":140568192,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1458661813","clinical_significance":[],"start":140568194,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140568194,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"id":"rs1585652986","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568198,"source":"dbSNP","strand":1,"feature_type":"variation","end":140568198,"alleles":["C","T"]},{"alleles":["T","C"],"end":140568199,"feature_type":"variation","strand":1,"source":"dbSNP","start":140568199,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797953486"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140568201,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568201,"clinical_significance":[],"seq_region_name":"7","id":"rs1797953611"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140568205,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568205,"clinical_significance":[],"seq_region_name":"7","id":"rs1339585759"},{"alleles":["C","G","T"],"end":140568206,"strand":1,"feature_type":"variation","start":140568206,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1009096573","clinical_significance":[]},{"alleles":["G","A","T"],"end":140568208,"strand":1,"feature_type":"variation","start":140568208,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1018657039","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs900221039","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568215,"feature_type":"variation","strand":1,"end":140568215,"alleles":["C","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568217,"feature_type":"variation","strand":1,"end":140568217,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1797954261"},{"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140568219,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568219,"source":"dbSNP","id":"rs1373919010","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs7780213","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568220,"feature_type":"variation","strand":1,"end":140568220,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797954677","alleles":["T","C"],"end":140568221,"feature_type":"variation","strand":1,"source":"dbSNP","start":140568221,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1032776810","seq_region_name":"7","end":140568222,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140568222,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140568227,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140568227,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1797954949","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1797955068","clinical_significance":[],"end":140568228,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140568228,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568229,"source":"dbSNP","strand":1,"feature_type":"variation","end":140568229,"alleles":["C","G"],"seq_region_name":"7","id":"rs907238627","clinical_significance":[]},{"id":"rs1002874036","seq_region_name":"7","clinical_significance":[],"alleles":["A","G"],"end":140568230,"strand":1,"feature_type":"variation","start":140568230,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1681786","source":"dbSNP","start":140568231,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C","T"],"end":140568231,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1797955795","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568232,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140568232},{"end":140568232,"alleles":["G","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140568232,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797955909"},{"source":"dbSNP","start":140568235,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140568235,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1474449165"},{"clinical_significance":[],"seq_region_name":"7","id":"rs894566071","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568236,"feature_type":"variation","strand":1,"end":140568236,"alleles":["G","A"]},{"alleles":["G","A"],"end":140568244,"feature_type":"variation","strand":1,"source":"dbSNP","start":140568244,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1305745040"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568246,"feature_type":"variation","strand":1,"end":140568246,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1437834813"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1274581147","alleles":["G","A"],"end":140568249,"feature_type":"variation","strand":1,"source":"dbSNP","start":140568249,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568253,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140568253,"clinical_significance":[],"seq_region_name":"7","id":"rs1797956530"},{"end":140568256,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140568256,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1193988274"},{"alleles":["G","T"],"end":140568272,"feature_type":"variation","strand":1,"source":"dbSNP","start":140568272,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1797956727","seq_region_name":"7"},{"source":"dbSNP","start":140568273,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140568273,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1006687490"},{"seq_region_name":"7","id":"rs988725130","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568276,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140568276},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568277,"source":"dbSNP","strand":1,"feature_type":"variation","end":140568281,"alleles":["AAAAA","AAAA"],"seq_region_name":"7","id":"rs2130596989","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs777169196","source":"dbSNP","start":140568298,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140568298,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568298,"source":"dbSNP","strand":1,"feature_type":"variation","end":140568300,"alleles":["AAA","AA"],"seq_region_name":"7","id":"rs1340695489","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797957359","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568300,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140568300},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568307,"source":"dbSNP","strand":1,"feature_type":"variation","end":140568307,"alleles":["G","T"],"seq_region_name":"7","id":"rs573128687","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140568308,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568308,"source":"dbSNP","seq_region_name":"7","id":"rs1353356497","clinical_significance":[]},{"clinical_significance":[],"id":"rs146245660","seq_region_name":"7","end":140568309,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140568309,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140568312,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140568312,"strand":1,"feature_type":"variation","id":"rs1797957798","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","T"],"end":140568313,"strand":1,"feature_type":"variation","start":140568313,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs962165058","clinical_significance":[]},{"alleles":["C","A"],"end":140568314,"feature_type":"variation","strand":1,"source":"dbSNP","start":140568314,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797958021"},{"alleles":["T","G"],"end":140568315,"feature_type":"variation","strand":1,"source":"dbSNP","start":140568315,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs982489548"},{"seq_region_name":"7","id":"rs1797958245","clinical_significance":[],"strand":1,"feature_type":"variation","end":140568320,"alleles":["TATTTA","TA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568315,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568316,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140568316,"clinical_significance":[],"seq_region_name":"7","id":"rs1797958353"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568318,"source":"dbSNP","strand":1,"feature_type":"variation","end":140568318,"alleles":["T","C"],"seq_region_name":"7","id":"rs2130597106","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797958471","source":"dbSNP","start":140568325,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140568325,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1333184910","clinical_significance":[],"strand":1,"feature_type":"variation","end":140568331,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568331,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140568332,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568332,"clinical_significance":[],"seq_region_name":"7","id":"rs1327000750"},{"end":140568335,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140568335,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs558946992","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797958943","source":"dbSNP","start":140568336,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140568336,"alleles":["G","A"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568339,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140568339,"clinical_significance":[],"seq_region_name":"7","id":"rs928038370"},{"seq_region_name":"7","id":"rs1797959140","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140568341,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568341,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568349,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140568349,"clinical_significance":[],"id":"rs938056924","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797959347","source":"dbSNP","start":140568353,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140568353,"alleles":["A","G"],"feature_type":"variation","strand":1},{"alleles":["C","T"],"end":140568365,"strand":1,"feature_type":"variation","start":140568365,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1459524032","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1417595055","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568369,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140568369},{"seq_region_name":"7","id":"rs577460047","clinical_significance":[],"alleles":["C","G"],"end":140568373,"strand":1,"feature_type":"variation","start":140568373,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1180917114","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568375,"source":"dbSNP","strand":1,"feature_type":"variation","end":140568375,"alleles":["A","C"]},{"start":140568381,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140568381,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797959854","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568395,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140568395,"clinical_significance":[],"seq_region_name":"7","id":"rs1470339445"},{"id":"rs1030532039","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568402,"source":"dbSNP","strand":1,"feature_type":"variation","end":140568402,"alleles":["T","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1179103303","source":"dbSNP","start":140568405,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140568405,"alleles":["A","T"],"feature_type":"variation","strand":1},{"id":"rs1456959126","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140568414,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568414,"source":"dbSNP"},{"source":"dbSNP","start":140568415,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140568415,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1563147475"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1273688283","source":"dbSNP","start":140568424,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140568424,"alleles":["G","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs955079919","clinical_significance":[],"strand":1,"feature_type":"variation","end":140568427,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568427,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1332324495","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568431,"source":"dbSNP","strand":1,"feature_type":"variation","end":140568431,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1288965805","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568432,"feature_type":"variation","strand":1,"end":140568432,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797960974","alleles":["G","A"],"end":140568437,"feature_type":"variation","strand":1,"source":"dbSNP","start":140568437,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs372769213","clinical_significance":[],"alleles":["G","A","C"],"end":140568440,"strand":1,"feature_type":"variation","start":140568440,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568449,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140568449,"seq_region_name":"7","id":"rs1424589626","clinical_significance":[]},{"end":140568451,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140568451,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1278034010","seq_region_name":"7"},{"alleles":["G","C"],"end":140568454,"strand":1,"feature_type":"variation","start":140568454,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1446064035","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130597322","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568457,"feature_type":"variation","strand":1,"end":140568457,"alleles":["G","C"]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140568458,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568458,"source":"dbSNP","seq_region_name":"7","id":"rs1797961470","clinical_significance":[]},{"seq_region_name":"7","id":"rs1189903286","clinical_significance":[],"alleles":["T","A"],"end":140568459,"strand":1,"feature_type":"variation","start":140568459,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797961694","feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140568468,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568468},{"clinical_significance":[],"seq_region_name":"7","id":"rs990999275","alleles":["A","G"],"end":140568469,"feature_type":"variation","strand":1,"source":"dbSNP","start":140568469,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs920748574","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568473,"source":"dbSNP","strand":1,"feature_type":"variation","end":140568473,"alleles":["T","G"]},{"seq_region_name":"7","id":"rs1797962056","clinical_significance":[],"start":140568474,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140568474,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140568475,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568475,"source":"dbSNP","id":"rs1585653501","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797962289","clinical_significance":[],"alleles":["T","C"],"end":140568481,"strand":1,"feature_type":"variation","start":140568481,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140568489,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140568489,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1371832888"},{"alleles":["A","C"],"end":140568494,"strand":1,"feature_type":"variation","start":140568494,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585653515","clinical_significance":[]},{"end":140568495,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140568495,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797962601","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs189542749","alleles":["C","T"],"end":140568496,"feature_type":"variation","strand":1,"source":"dbSNP","start":140568496,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568499,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140568499,"clinical_significance":[],"seq_region_name":"7","id":"rs867059317"},{"source":"dbSNP","start":140568502,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140568502,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs886655861"},{"alleles":["T","C"],"end":140568506,"strand":1,"feature_type":"variation","start":140568506,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1797963076","seq_region_name":"7","clinical_significance":[]},{"start":140568509,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140568509,"strand":1,"feature_type":"variation","id":"rs1797963179","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1160346202","alleles":["A","-"],"end":140568511,"feature_type":"variation","strand":1,"source":"dbSNP","start":140568511,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797963407","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140568514,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568514},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568515,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140568515,"clinical_significance":[],"seq_region_name":"7","id":"rs556314081"},{"seq_region_name":"7","id":"rs945857854","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568518,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140568518},{"alleles":["G","C"],"end":140568520,"strand":1,"feature_type":"variation","start":140568520,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1464061692","clinical_significance":[]},{"start":140568523,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140568523,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797963899","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140568530,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568530,"clinical_significance":[],"seq_region_name":"7","id":"rs1585653591"},{"seq_region_name":"7","id":"rs1438484670","clinical_significance":[],"start":140568531,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140568531,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1039992826","clinical_significance":[],"strand":1,"feature_type":"variation","end":140568532,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568532,"source":"dbSNP"},{"clinical_significance":[],"id":"rs900273406","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568537,"feature_type":"variation","strand":1,"end":140568537,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs995866512","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568538,"source":"dbSNP","strand":1,"feature_type":"variation","end":140568538,"alleles":["G","A","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797964580","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140568543,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568543},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568545,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140568545,"clinical_significance":[],"id":"rs2130597558","seq_region_name":"7"},{"start":140568548,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140568548,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797964687","clinical_significance":[]},{"alleles":["C","T"],"end":140568549,"feature_type":"variation","strand":1,"source":"dbSNP","start":140568549,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1216189513","seq_region_name":"7"},{"seq_region_name":"7","id":"rs928541940","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568553,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140568553},{"alleles":["A","T"],"end":140568562,"strand":1,"feature_type":"variation","start":140568562,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1797965048","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568567,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CT","CTCT"],"end":140568568,"seq_region_name":"7","id":"rs1797965153","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568569,"source":"dbSNP","strand":1,"feature_type":"variation","end":140568569,"alleles":["G","A"],"seq_region_name":"7","id":"rs1032829219","clinical_significance":[]},{"seq_region_name":"7","id":"rs1282349800","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140568583,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568583,"source":"dbSNP"},{"start":140568589,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140568589,"strand":1,"feature_type":"variation","id":"rs1585653716","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797965601","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568592,"source":"dbSNP","strand":1,"feature_type":"variation","end":140568592,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1239698705","feature_type":"variation","strand":1,"alleles":["T","A"],"end":140568593,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568593},{"clinical_significance":[],"seq_region_name":"7","id":"rs114564169","alleles":["C","A","T"],"end":140568596,"feature_type":"variation","strand":1,"source":"dbSNP","start":140568596,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568597,"source":"dbSNP","strand":1,"feature_type":"variation","end":140568597,"alleles":["G","A","T"],"seq_region_name":"7","id":"rs551015602","clinical_significance":[]},{"id":"rs2130597667","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568598,"source":"dbSNP","strand":1,"feature_type":"variation","end":140568598,"alleles":["G","A"]},{"start":140568601,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140568601,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","id":"rs1020210776","seq_region_name":"7","clinical_significance":[]},{"start":140568602,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140568602,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs542279254","clinical_significance":[]},{"id":"rs1797966403","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140568604,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568604,"source":"dbSNP"},{"seq_region_name":"7","id":"rs2130597707","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568605,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140568605},{"clinical_significance":[],"seq_region_name":"7","id":"rs1343819343","source":"dbSNP","start":140568608,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140568608,"feature_type":"variation","strand":1},{"id":"rs982130374","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140568612,"strand":1,"feature_type":"variation","start":140568612,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140568614,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140568614,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs993622192","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797966740","clinical_significance":[],"end":140568615,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140568615,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1034989822","clinical_significance":[],"start":140568617,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140568617,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140568622,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568622,"clinical_significance":[],"id":"rs1175028957","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs560959253","source":"dbSNP","start":140568635,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140568635,"alleles":["C","T"],"feature_type":"variation","strand":1},{"alleles":["G","A","C"],"end":140568636,"feature_type":"variation","strand":1,"source":"dbSNP","start":140568636,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs890721910","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs990884953","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568641,"feature_type":"variation","strand":1,"end":140568641,"alleles":["G","A"]},{"source":"dbSNP","start":140568643,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140568643,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1017963832","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs920803185","end":140568646,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140568646,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs930835191","clinical_significance":[],"end":140568647,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140568647,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1282522966","end":140568649,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140568649,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140568653,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568653,"source":"dbSNP","seq_region_name":"7","id":"rs967081820","clinical_significance":[]},{"id":"rs1296855375","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568654,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140568654},{"alleles":["A","G"],"end":140568655,"strand":1,"feature_type":"variation","start":140568655,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585653926","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140568657,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568657,"source":"dbSNP","seq_region_name":"7","id":"rs983986037","clinical_significance":[]},{"seq_region_name":"7","id":"rs1475039005","clinical_significance":[],"end":140568662,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140568662,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140568665,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568665,"clinical_significance":[],"seq_region_name":"7","id":"rs1194111378"},{"source":"dbSNP","start":140568666,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140568666,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs908136412"},{"alleles":["G","A"],"end":140568671,"strand":1,"feature_type":"variation","start":140568671,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs977262285","clinical_significance":[]},{"clinical_significance":[],"id":"rs114619340","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568673,"feature_type":"variation","strand":1,"end":140568673,"alleles":["C","T"]},{"end":140568674,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140568674,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs771974379","clinical_significance":[]},{"alleles":["C","T"],"end":140568675,"feature_type":"variation","strand":1,"source":"dbSNP","start":140568675,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797969009"},{"end":140568678,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140568678,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585653988","clinical_significance":[]},{"id":"rs1464053986","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140568680,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568680,"source":"dbSNP"},{"id":"rs1797969295","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140568683,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568683,"source":"dbSNP"},{"end":140568684,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140568684,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1359169058"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568686,"source":"dbSNP","strand":1,"feature_type":"variation","end":140568686,"alleles":["C","T"],"seq_region_name":"7","id":"rs1797969483","clinical_significance":[]},{"clinical_significance":[],"id":"rs1797969593","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568688,"feature_type":"variation","strand":1,"end":140568688,"alleles":["T","C","G"]},{"id":"rs1797969718","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140568689,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568689,"source":"dbSNP"},{"start":140568691,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140568691,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1358076122","clinical_significance":[]},{"start":140568697,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140568697,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797969940","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797970062","source":"dbSNP","start":140568698,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140568698,"alleles":["G","A"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568701,"feature_type":"variation","strand":1,"end":140568701,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1171053475"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585654029","alleles":["G","T"],"end":140568702,"feature_type":"variation","strand":1,"source":"dbSNP","start":140568702,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs938629601","seq_region_name":"7","end":140568704,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140568704,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140568707,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568707,"clinical_significance":[],"id":"rs1797970553","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs747392784","alleles":["G","A"],"end":140568712,"feature_type":"variation","strand":1,"source":"dbSNP","start":140568712,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140568716,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140568716,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1421173410","seq_region_name":"7"},{"source":"dbSNP","start":140568717,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140568717,"alleles":["T","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs757752348"},{"start":140568718,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140568718,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130598025","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568724,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140568724,"clinical_significance":[],"id":"rs1329980382","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1210627724","clinical_significance":[],"end":140568725,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140568725,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1240603783","seq_region_name":"7","feature_type":"variation","strand":1,"end":140568727,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568727},{"source":"dbSNP","start":140568731,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140568731,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1485632844"},{"clinical_significance":[],"seq_region_name":"7","id":"rs371140994","end":140568734,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140568734,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797971871","source":"dbSNP","start":140568738,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140568738,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140568741,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C","T"],"end":140568741,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs746117036"},{"seq_region_name":"7","id":"rs375400818","clinical_significance":[],"end":140568744,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140568744,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1797972228","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140568745,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568745,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568749,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140568749,"clinical_significance":[],"seq_region_name":"7","id":"rs1563147722"},{"clinical_significance":[],"seq_region_name":"7","id":"rs775450431","source":"dbSNP","start":140568750,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140568750,"feature_type":"variation","strand":1},{"alleles":["G","T"],"end":140568752,"feature_type":"variation","strand":1,"source":"dbSNP","start":140568752,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs748074080"},{"clinical_significance":[],"id":"rs1413298230","seq_region_name":"7","source":"dbSNP","start":140568760,"consequence_type":"splice_donor_region_variant","assembly_name":"GRCh38","end":140568760,"alleles":["C","T"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140568767,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140568767,"seq_region_name":"7","id":"rs771998967","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1198965481","source":"dbSNP","start":140568772,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140568772,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["CTCCTC","CTC"],"end":140568778,"assembly_name":"GRCh38","consequence_type":"inframe_deletion","start":140568773,"source":"dbSNP","seq_region_name":"7","id":"rs1160587681","clinical_significance":[]},{"alleles":["C","G"],"end":140568775,"strand":1,"feature_type":"variation","start":140568775,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs1482931534","clinical_significance":[]},{"end":140568778,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140568778,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs1797973198","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797973326","clinical_significance":[],"strand":1,"feature_type":"variation","end":140568779,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140568779,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140568780,"source":"dbSNP","strand":1,"feature_type":"variation","end":140568780,"alleles":["G","A"],"seq_region_name":"7","id":"rs201174441","clinical_significance":[]},{"end":140568783,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140568783,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1252037156"},{"alleles":["A","G"],"end":140568785,"feature_type":"variation","strand":1,"source":"dbSNP","start":140568785,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797973697"},{"clinical_significance":[],"seq_region_name":"7","id":"rs760461662","end":140568786,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140568786,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"id":"rs1474949486","seq_region_name":"7","clinical_significance":[],"alleles":["C","G"],"end":140568790,"strand":1,"feature_type":"variation","start":140568790,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797974077","end":140568793,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140568793,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"start":140568796,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["C","T"],"end":140568796,"strand":1,"feature_type":"variation","id":"rs1797974192","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140568797,"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140568797,"source":"dbSNP","seq_region_name":"7","id":"rs1797974312","clinical_significance":[]},{"seq_region_name":"7","id":"rs1207230785","clinical_significance":[],"end":140568798,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140568798,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs766204304","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568800,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140568800},{"id":"rs1797974671","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140568803,"strand":1,"feature_type":"variation","start":140568803,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant"},{"start":140568809,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","end":140568809,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130598248","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1197649046","feature_type":"variation","strand":1,"end":140568814,"alleles":["C","T"],"consequence_type":"splice_acceptor_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568814},{"clinical_significance":[],"seq_region_name":"7","id":"rs867316870","alleles":["G","A"],"end":140568817,"feature_type":"variation","strand":1,"source":"dbSNP","start":140568817,"consequence_type":"splice_region_variant","assembly_name":"GRCh38"},{"consequence_type":"splice_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568818,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140568818,"clinical_significance":[],"seq_region_name":"7","id":"rs1306318861"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140568821,"consequence_type":"splice_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568821,"clinical_significance":[],"seq_region_name":"7","id":"rs1347227971"},{"seq_region_name":"7","id":"rs1797975155","clinical_significance":[],"strand":1,"feature_type":"variation","end":140568827,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"splice_polypyrimidine_tract_variant","start":140568827,"source":"dbSNP"},{"alleles":["G","A"],"end":140568832,"feature_type":"variation","strand":1,"source":"dbSNP","start":140568832,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs776328741"},{"id":"rs1277930984","seq_region_name":"7","clinical_significance":[],"start":140568837,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140568837,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs565073836","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568839,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140568839},{"clinical_significance":[],"seq_region_name":"7","id":"rs1350982472","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140568840,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568840},{"seq_region_name":"7","id":"rs1797975708","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568842,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140568842},{"id":"rs1357771144","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140568846,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568846,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1230320817","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568850,"source":"dbSNP","strand":1,"feature_type":"variation","end":140568850,"alleles":["G","T"]},{"clinical_significance":[],"id":"rs915940858","seq_region_name":"7","source":"dbSNP","start":140568851,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140568851,"alleles":["A","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs764764816","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568852,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140568852},{"seq_region_name":"7","id":"rs752154011","clinical_significance":[],"start":140568853,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140568853,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["TTCTTCT","TTCT"],"end":140568859,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568853,"clinical_significance":[],"id":"rs3833488","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797976386","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568855,"feature_type":"variation","strand":1,"end":140568855,"alleles":["C","T"]},{"alleles":["T","G"],"end":140568857,"feature_type":"variation","strand":1,"source":"dbSNP","start":140568857,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs758919421","seq_region_name":"7"},{"id":"rs764685723","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140568860,"strand":1,"feature_type":"variation","start":140568860,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1489974216","source":"dbSNP","start":140568861,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140568861,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs368374570","source":"dbSNP","start":140568865,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140568865,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797976973","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140568866,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568866},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797977086","feature_type":"variation","strand":1,"end":140568870,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568870},{"end":140568872,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140568872,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1463430560"},{"clinical_significance":[],"id":"rs1797977295","seq_region_name":"7","source":"dbSNP","start":140568872,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TCTTTCT","TCT"],"end":140568878,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1054123889","end":140568876,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140568876,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs929358754","end":140568878,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140568878,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140568880,"alleles":["T","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568880,"source":"dbSNP","seq_region_name":"7","id":"rs892844771","clinical_significance":[]},{"clinical_significance":[],"id":"rs1797977741","seq_region_name":"7","source":"dbSNP","start":140568887,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140568887,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs527462244","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568889,"source":"dbSNP","strand":1,"feature_type":"variation","end":140568889,"alleles":["A","G"]},{"strand":1,"feature_type":"variation","end":140568890,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568890,"source":"dbSNP","id":"rs1051901433","seq_region_name":"7","clinical_significance":[]},{"id":"rs1563147885","seq_region_name":"7","clinical_significance":[],"start":140568891,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140568891,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1461720900","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568892,"source":"dbSNP","strand":1,"feature_type":"variation","end":140568892,"alleles":["G","A","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797978309","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140568898,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568898},{"clinical_significance":[],"seq_region_name":"7","id":"rs1041921220","end":140568900,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140568900,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140568902,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140568902,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585654504"},{"seq_region_name":"7","id":"rs907133487","clinical_significance":[],"alleles":["C","G"],"end":140568903,"strand":1,"feature_type":"variation","start":140568903,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1797978758","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568905,"feature_type":"variation","strand":1,"end":140568905,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs1585654519","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140568909,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568909,"source":"dbSNP"},{"source":"dbSNP","start":140568911,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140568911,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1797978965"},{"clinical_significance":[],"seq_region_name":"7","id":"rs149969470","alleles":["G","A"],"end":140568916,"feature_type":"variation","strand":1,"source":"dbSNP","start":140568916,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1251310420","source":"dbSNP","start":140568920,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140568920,"alleles":["T","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1035042133","clinical_significance":[],"end":140568924,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140568924,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["T","C"],"end":140568930,"strand":1,"feature_type":"variation","start":140568930,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1797979425","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140568932,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TTTTTTTTTTT","TTTTTTTTTT","TTTTTTTTTTTT"],"end":140568942,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs761913427"},{"strand":1,"feature_type":"variation","end":140568943,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568943,"source":"dbSNP","id":"rs181145172","seq_region_name":"7","clinical_significance":[]},{"end":140568947,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140568947,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797979847","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797979964","alleles":["G","A"],"end":140568948,"feature_type":"variation","strand":1,"source":"dbSNP","start":140568948,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568950,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140568950,"seq_region_name":"7","id":"rs1797980071","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568952,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140568952,"id":"rs1585654593","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs977144283","clinical_significance":[],"alleles":["C","G"],"end":140568953,"strand":1,"feature_type":"variation","start":140568953,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140568955,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140568955,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1242129177","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797980431","end":140568956,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140568956,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568970,"source":"dbSNP","strand":1,"feature_type":"variation","end":140568970,"alleles":["G","A","T"],"seq_region_name":"7","id":"rs1339543656","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs530240992","end":140568973,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140568973,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568976,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140568976,"seq_region_name":"7","id":"rs1797980740","clinical_significance":[]},{"start":140568977,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140568977,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1312791530","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797980929","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568979,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140568979},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568980,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140568980,"seq_region_name":"7","id":"rs2130598678","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568981,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140568981,"id":"rs1235499154","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs548348908","seq_region_name":"7","end":140568985,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140568985,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1485451785","end":140568986,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140568986,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1441635023","seq_region_name":"7","clinical_significance":[],"start":140568989,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140568989,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs2130598725","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140568990,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568990,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568991,"source":"dbSNP","strand":1,"feature_type":"variation","end":140568991,"alleles":["C","G"],"id":"rs1797981422","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1217689129","alleles":["C","A","T"],"end":140568993,"feature_type":"variation","strand":1,"source":"dbSNP","start":140568993,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140568994,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140568994,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1161296344","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140568995,"source":"dbSNP","strand":1,"feature_type":"variation","end":140568995,"alleles":["G","A"],"seq_region_name":"7","id":"rs1797982088","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140568996,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140568996,"clinical_significance":[],"seq_region_name":"7","id":"rs1457567929"},{"source":"dbSNP","start":140569001,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140569001,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1797982264","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs550668361","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569003,"feature_type":"variation","strand":1,"end":140569003,"alleles":["C","A"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569004,"source":"dbSNP","strand":1,"feature_type":"variation","end":140569005,"alleles":["AA","A"],"seq_region_name":"7","id":"rs1364562109","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569005,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140569005,"clinical_significance":[],"seq_region_name":"7","id":"rs1585654740"},{"clinical_significance":[],"seq_region_name":"7","id":"rs566870050","source":"dbSNP","start":140569006,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140569006,"alleles":["C","G"],"feature_type":"variation","strand":1},{"id":"rs533982142","seq_region_name":"7","clinical_significance":[],"end":140569010,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140569010,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585654767","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140569012,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569012},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797982927","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140569017,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569017},{"seq_region_name":"7","id":"rs1797983028","clinical_significance":[],"end":140569018,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140569018,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140569020,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569020,"clinical_significance":[],"seq_region_name":"7","id":"rs1797983139"},{"source":"dbSNP","start":140569023,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140569023,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1035543250"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569024,"source":"dbSNP","strand":1,"feature_type":"variation","end":140569024,"alleles":["C","T"],"seq_region_name":"7","id":"rs1012372842","clinical_significance":[]},{"start":140569025,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140569025,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1480413516","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1237714617","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569026,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140569026},{"clinical_significance":[],"seq_region_name":"7","id":"rs1194789654","end":140569032,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140569032,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs145171677","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569035,"source":"dbSNP","strand":1,"feature_type":"variation","end":140569035,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797983951","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140569036,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569036},{"alleles":["G","C"],"end":140569037,"feature_type":"variation","strand":1,"source":"dbSNP","start":140569037,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs991455342","seq_region_name":"7"},{"start":140569043,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140569043,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1797984166","clinical_significance":[]},{"seq_region_name":"7","id":"rs1797984241","clinical_significance":[],"alleles":["C","T"],"end":140569047,"strand":1,"feature_type":"variation","start":140569047,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs148725609","clinical_significance":[],"alleles":["C","G"],"end":140569048,"strand":1,"feature_type":"variation","start":140569048,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140569049,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569049,"source":"dbSNP","id":"rs1797984487","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797984586","source":"dbSNP","start":140569049,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TGAGT","T"],"end":140569053,"feature_type":"variation","strand":1},{"alleles":["G","A"],"end":140569052,"feature_type":"variation","strand":1,"source":"dbSNP","start":140569052,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1351873717","seq_region_name":"7"},{"alleles":["T","C"],"end":140569053,"feature_type":"variation","strand":1,"source":"dbSNP","start":140569053,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1260886417"},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140569055,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569055,"clinical_significance":[],"seq_region_name":"7","id":"rs1797985073"},{"start":140569058,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140569058,"strand":1,"feature_type":"variation","id":"rs2130598981","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569064,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140569064,"seq_region_name":"7","id":"rs1797985229","clinical_significance":[]},{"start":140569065,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140569065,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1241880289","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs538130193","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140569070,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569070},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130599008","source":"dbSNP","start":140569073,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140569073,"alleles":["T","C"],"feature_type":"variation","strand":1},{"end":140569075,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140569075,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1307976550"},{"start":140569078,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140569078,"strand":1,"feature_type":"variation","id":"rs1797985984","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140569079,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140569079,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585654932"},{"clinical_significance":[],"seq_region_name":"7","id":"rs908022531","feature_type":"variation","strand":1,"end":140569080,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569080},{"clinical_significance":[],"id":"rs1373149675","seq_region_name":"7","source":"dbSNP","start":140569081,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140569081,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["-","A"],"end":140569084,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569085,"clinical_significance":[],"seq_region_name":"7","id":"rs1797986663"},{"id":"rs1321541788","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140569085,"alleles":["T","A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569085,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs973382557","feature_type":"variation","strand":1,"end":140569088,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569088},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569100,"source":"dbSNP","strand":1,"feature_type":"variation","end":140569100,"alleles":["T","A"],"seq_region_name":"7","id":"rs1797987217","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["TTTTTT","TTTTT"],"end":140569105,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569100,"clinical_significance":[],"seq_region_name":"7","id":"rs1797987363"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569105,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140569105,"seq_region_name":"7","id":"rs919237249","clinical_significance":[]},{"end":140569108,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140569108,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs929417742"},{"clinical_significance":[],"seq_region_name":"7","id":"rs185504306","source":"dbSNP","start":140569110,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140569110,"feature_type":"variation","strand":1},{"end":140569112,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140569112,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797987792","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs144632483","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569123,"feature_type":"variation","strand":1,"end":140569123,"alleles":["G","A"]},{"start":140569127,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140569127,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1379742243","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1174377171","feature_type":"variation","strand":1,"end":140569128,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569128},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797988251","feature_type":"variation","strand":1,"alleles":["TGGTATAA","-"],"end":140569146,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569139},{"seq_region_name":"7","id":"rs1585655060","clinical_significance":[],"start":140569142,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140569142,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140569143,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569143,"clinical_significance":[],"seq_region_name":"7","id":"rs912097615"},{"strand":1,"feature_type":"variation","end":140569145,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569145,"source":"dbSNP","seq_region_name":"7","id":"rs116550758","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["AA","CG"],"end":140569146,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569145,"clinical_significance":[],"seq_region_name":"7","id":"rs373311092"},{"alleles":["A","G"],"end":140569146,"strand":1,"feature_type":"variation","start":140569146,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs116038686","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1554470473","alleles":["AA","CG"],"end":140569147,"feature_type":"variation","strand":1,"source":"dbSNP","start":140569146,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140569152,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569152,"source":"dbSNP","seq_region_name":"7","id":"rs931658410","clinical_significance":[]},{"alleles":["A","C"],"end":140569155,"feature_type":"variation","strand":1,"source":"dbSNP","start":140569155,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1585655127","seq_region_name":"7"},{"clinical_significance":[],"id":"rs190319435","seq_region_name":"7","feature_type":"variation","strand":1,"end":140569160,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569160},{"seq_region_name":"7","id":"rs1218330007","clinical_significance":[],"strand":1,"feature_type":"variation","end":140569161,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569161,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1797989394","seq_region_name":"7","alleles":["A","G"],"end":140569166,"feature_type":"variation","strand":1,"source":"dbSNP","start":140569166,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs914347814","clinical_significance":[],"strand":1,"feature_type":"variation","end":140569167,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569167,"source":"dbSNP"},{"seq_region_name":"7","id":"rs147895470","clinical_significance":[],"alleles":["C","T"],"end":140569169,"strand":1,"feature_type":"variation","start":140569169,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["G","A"],"end":140569170,"strand":1,"feature_type":"variation","start":140569170,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs764867825","clinical_significance":[]},{"clinical_significance":[],"id":"rs1797989838","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140569171,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569171},{"source":"dbSNP","start":140569179,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140569179,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1563148112"},{"id":"rs1011131019","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140569182,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569182,"source":"dbSNP"},{"id":"rs1272945179","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569190,"source":"dbSNP","strand":1,"feature_type":"variation","end":140569190,"alleles":["G","C"]},{"alleles":["C","T"],"end":140569206,"strand":1,"feature_type":"variation","start":140569206,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs568961","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs551651247","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140569207,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569207,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569209,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140569209,"clinical_significance":[],"seq_region_name":"7","id":"rs1797990605"},{"seq_region_name":"7","id":"rs1297517992","clinical_significance":[],"strand":1,"feature_type":"variation","end":140569211,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569211,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1055713305","clinical_significance":[],"start":140569216,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140569216,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs532463647","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140569217,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569217},{"alleles":["C","G","T"],"end":140569218,"strand":1,"feature_type":"variation","start":140569218,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs758034447","clinical_significance":[]},{"start":140569219,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140569219,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs1797991086","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130599323","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569221,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140569221},{"seq_region_name":"7","id":"rs1012271339","clinical_significance":[],"end":140569223,"alleles":["C","A","G","T"],"strand":1,"feature_type":"variation","start":140569223,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs590083","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569224,"feature_type":"variation","strand":1,"end":140569224,"alleles":["G","A","T"]},{"id":"rs1375121466","seq_region_name":"7","clinical_significance":[],"alleles":["TTGTTGT","TTGT"],"end":140569235,"strand":1,"feature_type":"variation","start":140569229,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140569231,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140569231,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs562677241"},{"start":140569232,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140569232,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1477717828","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs147078514","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569236,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140569236},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569237,"source":"dbSNP","strand":1,"feature_type":"variation","end":140569242,"alleles":["TCTTTC","TC"],"seq_region_name":"7","id":"rs1797991942","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585655409","source":"dbSNP","start":140569239,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TTT","TT"],"end":140569241,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1797992166","clinical_significance":[],"strand":1,"feature_type":"variation","end":140569244,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569244,"source":"dbSNP"},{"end":140569246,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140569246,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1211177159"},{"id":"rs1797992371","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140569247,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569247,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1022763160","end":140569248,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140569248,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140569250,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569250,"clinical_significance":[],"seq_region_name":"7","id":"rs1015130578"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140569255,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569255,"source":"dbSNP","seq_region_name":"7","id":"rs1797992728","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140569258,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569258,"clinical_significance":[],"id":"rs1797992842","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1199784064","source":"dbSNP","start":140569261,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140569261,"alleles":["C","T"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569262,"feature_type":"variation","strand":1,"end":140569262,"alleles":["G","A"],"clinical_significance":[],"id":"rs1340036522","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1797993133","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569263,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","-"],"end":140569263},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569264,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140569264,"clinical_significance":[],"seq_region_name":"7","id":"rs1797993229"},{"id":"rs548358262","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569266,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140569266},{"clinical_significance":[],"seq_region_name":"7","id":"rs1216513735","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569267,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140569267},{"id":"rs1797993577","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140569268,"strand":1,"feature_type":"variation","start":140569268,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1439775975","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569269,"source":"dbSNP","strand":1,"feature_type":"variation","end":140569269,"alleles":["C","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1294059963","end":140569271,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140569271,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs777140314","clinical_significance":[],"alleles":["C","T"],"end":140569275,"strand":1,"feature_type":"variation","start":140569275,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140569276,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140569276,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1585655502","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569281,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140569281,"clinical_significance":[],"seq_region_name":"7","id":"rs1797994167"},{"end":140569283,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140569283,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797994260"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569284,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140569284,"clinical_significance":[],"seq_region_name":"7","id":"rs1405330463"},{"source":"dbSNP","start":140569288,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140569288,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1797994461","seq_region_name":"7"},{"source":"dbSNP","start":140569289,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140569289,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1333652885"},{"clinical_significance":[],"id":"rs1797994653","seq_region_name":"7","end":140569301,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140569301,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs2130599583","clinical_significance":[],"alleles":["A","G"],"end":140569310,"strand":1,"feature_type":"variation","start":140569310,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140569313,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140569313,"alleles":["G","C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1410991579","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569321,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140569321,"clinical_significance":[],"seq_region_name":"7","id":"rs1169192256"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569329,"source":"dbSNP","strand":1,"feature_type":"variation","end":140569329,"alleles":["A","G"],"seq_region_name":"7","id":"rs1465379847","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585655557","clinical_significance":[],"start":140569330,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140569330,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1797995177","seq_region_name":"7","source":"dbSNP","start":140569332,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140569332,"alleles":["T","C"],"feature_type":"variation","strand":1},{"start":140569342,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140569342,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs973275751","clinical_significance":[]},{"end":140569348,"alleles":["AGA","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140569346,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585655579"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1188203178","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569348,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140569348},{"end":140569353,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140569353,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1797995667"},{"alleles":["G","A"],"end":140569357,"feature_type":"variation","strand":1,"source":"dbSNP","start":140569357,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs534090027"},{"seq_region_name":"7","id":"rs183058069","clinical_significance":[],"start":140569358,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140569358,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797995979","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569358,"feature_type":"variation","strand":1,"end":140569361,"alleles":["CCCC","CCC"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1186174662","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140569359,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569359},{"seq_region_name":"7","id":"rs1797996188","clinical_significance":[],"alleles":["T","C"],"end":140569365,"strand":1,"feature_type":"variation","start":140569365,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1797996278","clinical_significance":[],"end":140569366,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140569366,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569368,"feature_type":"variation","strand":1,"end":140569368,"alleles":["G","T"],"clinical_significance":[],"id":"rs1797996387","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569369,"feature_type":"variation","strand":1,"end":140569369,"alleles":["C","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1797996481"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569370,"source":"dbSNP","strand":1,"feature_type":"variation","end":140569370,"alleles":["A","G"],"seq_region_name":"7","id":"rs989847299","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140569379,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569379,"clinical_significance":[],"seq_region_name":"7","id":"rs1259844284"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140569381,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569381,"source":"dbSNP","seq_region_name":"7","id":"rs1350885503","clinical_significance":[]},{"seq_region_name":"7","id":"rs1317063975","clinical_significance":[],"strand":1,"feature_type":"variation","end":140569382,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569382,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140569386,"alleles":["G","A","C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569386,"source":"dbSNP","seq_region_name":"7","id":"rs1463433452","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569387,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140569387,"seq_region_name":"7","id":"rs1324511545","clinical_significance":[]},{"seq_region_name":"7","id":"rs555327198","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140569390,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569390,"source":"dbSNP"},{"id":"rs1447589505","seq_region_name":"7","clinical_significance":[],"start":140569391,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140569391,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569396,"feature_type":"variation","strand":1,"end":140569402,"alleles":["CAGTCAG","CAGTCAGTCAG"],"clinical_significance":[],"seq_region_name":"7","id":"rs943436492"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569400,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140569400,"seq_region_name":"7","id":"rs1797997660","clinical_significance":[]},{"id":"rs1797997771","seq_region_name":"7","clinical_significance":[],"alleles":["A","G"],"end":140569401,"strand":1,"feature_type":"variation","start":140569401,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140569402,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140569402,"strand":1,"feature_type":"variation","id":"rs945839743","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs915386376","source":"dbSNP","start":140569407,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140569407,"alleles":["G","T"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140569411,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569411,"source":"dbSNP","seq_region_name":"7","id":"rs1395641810","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1797998205","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569414,"feature_type":"variation","strand":1,"end":140569414,"alleles":["C","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569421,"source":"dbSNP","strand":1,"feature_type":"variation","end":140569421,"alleles":["G","T"],"seq_region_name":"7","id":"rs1167400068","clinical_significance":[]},{"alleles":["G","C"],"end":140569423,"feature_type":"variation","strand":1,"source":"dbSNP","start":140569423,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1403983672"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569430,"source":"dbSNP","strand":1,"feature_type":"variation","end":140569430,"alleles":["T","A"],"seq_region_name":"7","id":"rs1411112590","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs781551276","source":"dbSNP","start":140569432,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140569432,"alleles":["G","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1563148270","clinical_significance":[],"strand":1,"feature_type":"variation","end":140569435,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569435,"source":"dbSNP"},{"id":"rs1585655801","seq_region_name":"7","clinical_significance":[],"end":140569436,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140569436,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["A","G"],"end":140569442,"strand":1,"feature_type":"variation","start":140569442,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797998859","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs928522409","feature_type":"variation","strand":1,"end":140569443,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569443},{"clinical_significance":[],"seq_region_name":"7","id":"rs1470138125","alleles":["A","G"],"end":140569447,"feature_type":"variation","strand":1,"source":"dbSNP","start":140569447,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140569458,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569458,"clinical_significance":[],"id":"rs1239531724","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1797999261","clinical_significance":[],"strand":1,"feature_type":"variation","end":140569460,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569460,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569466,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140569466,"id":"rs1585655832","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","G"],"end":140569468,"strand":1,"feature_type":"variation","start":140569468,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1797999484","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569470,"feature_type":"variation","strand":1,"end":140569470,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1797999589"},{"strand":1,"feature_type":"variation","end":140569473,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569473,"source":"dbSNP","id":"rs1797999683","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs938504563","end":140569475,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140569475,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs570476108","source":"dbSNP","start":140569477,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140569477,"alleles":["C","T"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140569478,"alleles":["G","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569478,"clinical_significance":[],"seq_region_name":"7","id":"rs538167336"},{"seq_region_name":"7","id":"rs931205411","clinical_significance":[],"alleles":["C","T"],"end":140569485,"strand":1,"feature_type":"variation","start":140569485,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585655871","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569486,"feature_type":"variation","strand":1,"end":140569486,"alleles":["T","C"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569490,"feature_type":"variation","strand":1,"end":140569490,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1290265453"},{"start":140569491,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140569491,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs902882827","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs548925004","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569492,"feature_type":"variation","strand":1,"end":140569492,"alleles":["C","G"]},{"source":"dbSNP","start":140569493,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140569493,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798000749"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1355945228","source":"dbSNP","start":140569494,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140569494,"alleles":["C","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs568324494","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569496,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140569496},{"seq_region_name":"7","id":"rs1240015484","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140569497,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569497,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140569502,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569502,"source":"dbSNP","seq_region_name":"7","id":"rs1798001218","clinical_significance":[]},{"end":140569509,"alleles":["AAA","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140569507,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1798001325","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798001420","alleles":["G","A"],"end":140569510,"feature_type":"variation","strand":1,"source":"dbSNP","start":140569510,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1272488391","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569511,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140569511},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140569512,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569512,"clinical_significance":[],"seq_region_name":"7","id":"rs1372311038"},{"id":"rs1458205079","seq_region_name":"7","clinical_significance":[],"alleles":["T","G"],"end":140569515,"strand":1,"feature_type":"variation","start":140569515,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569517,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140569517,"clinical_significance":[],"seq_region_name":"7","id":"rs113136645"},{"end":140569518,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140569518,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1015428957"},{"clinical_significance":[],"seq_region_name":"7","id":"rs554340074","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569520,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140569520},{"id":"rs1798002269","seq_region_name":"7","clinical_significance":[],"end":140569525,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140569525,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["A","G"],"end":140569527,"feature_type":"variation","strand":1,"source":"dbSNP","start":140569527,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs763147892"},{"feature_type":"variation","strand":1,"end":140569528,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569528,"clinical_significance":[],"seq_region_name":"7","id":"rs572886726"},{"strand":1,"feature_type":"variation","end":140569534,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569534,"source":"dbSNP","id":"rs186221389","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140569536,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569536,"source":"dbSNP","seq_region_name":"7","id":"rs1798002715","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140569538,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569538,"source":"dbSNP","seq_region_name":"7","id":"rs997658390","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569539,"feature_type":"variation","strand":1,"end":140569539,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1798002940"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798003018","feature_type":"variation","strand":1,"end":140569540,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569540},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130600214","end":140569546,"alleles":["TTCT","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140569543,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs774250902","clinical_significance":[],"start":140569545,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["CTCCTCCT","CTCCT"],"end":140569552,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569547,"feature_type":"variation","strand":1,"end":140569547,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1798003239"},{"clinical_significance":[],"id":"rs776310294","seq_region_name":"7","alleles":["T","C"],"end":140569549,"feature_type":"variation","strand":1,"source":"dbSNP","start":140569549,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","T"],"end":140569550,"feature_type":"variation","strand":1,"source":"dbSNP","start":140569550,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs963230192"},{"seq_region_name":"7","id":"rs1798003567","clinical_significance":[],"start":140569553,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140569553,"strand":1,"feature_type":"variation"},{"id":"rs558291887","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569555,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140569555},{"id":"rs2130600276","seq_region_name":"7","clinical_significance":[],"start":140569556,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140569556,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140569557,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569557,"source":"dbSNP","seq_region_name":"7","id":"rs73483908","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569560,"source":"dbSNP","strand":1,"feature_type":"variation","end":140569560,"alleles":["C","G","T"],"seq_region_name":"7","id":"rs950598809","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798004049","clinical_significance":[],"alleles":["AAAAAA","AAAAA"],"end":140569573,"strand":1,"feature_type":"variation","start":140569568,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140569572,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140569572,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs544530011"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1163295254","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569574,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140569574},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569575,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","-"],"end":140569575,"seq_region_name":"7","id":"rs1798004396","clinical_significance":[]},{"seq_region_name":"7","id":"rs562813285","clinical_significance":[],"alleles":["G","A"],"end":140569576,"strand":1,"feature_type":"variation","start":140569576,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569577,"source":"dbSNP","strand":1,"feature_type":"variation","end":140569577,"alleles":["G","T"],"id":"rs1798004601","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798004718","end":140569578,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140569578,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798004822","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569581,"feature_type":"variation","strand":1,"end":140569581,"alleles":["C","A"]},{"seq_region_name":"7","id":"rs1348698983","clinical_significance":[],"alleles":["C","T"],"end":140569582,"strand":1,"feature_type":"variation","start":140569582,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140569583,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140569583,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1798004999","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1798005106","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569587,"source":"dbSNP","strand":1,"feature_type":"variation","end":140569587,"alleles":["C","G"]},{"seq_region_name":"7","id":"rs1798005215","clinical_significance":[],"end":140569589,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140569589,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1303961668","seq_region_name":"7","clinical_significance":[],"alleles":["AAA","AAAA"],"end":140569593,"strand":1,"feature_type":"variation","start":140569591,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140569594,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569594,"clinical_significance":[],"seq_region_name":"7","id":"rs757662551"},{"seq_region_name":"7","id":"rs1473823210","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569595,"source":"dbSNP","strand":1,"feature_type":"variation","end":140569595,"alleles":["A","C"]},{"seq_region_name":"7","id":"rs774435170","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569597,"source":"dbSNP","strand":1,"feature_type":"variation","end":140569597,"alleles":["T","C"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569600,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","G"],"end":140569600,"id":"rs1178431567","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1405247977","clinical_significance":[],"end":140569603,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140569603,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569604,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140569604,"seq_region_name":"7","id":"rs372435783","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569605,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140569605,"clinical_significance":[],"seq_region_name":"7","id":"rs746053700"},{"feature_type":"variation","strand":1,"end":140569606,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569606,"clinical_significance":[],"seq_region_name":"7","id":"rs375408896"},{"clinical_significance":[],"seq_region_name":"7","id":"rs369364119","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140569607,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569607},{"clinical_significance":[],"seq_region_name":"7","id":"rs1302242573","source":"dbSNP","start":140569608,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140569608,"alleles":["A","G"],"feature_type":"variation","strand":1},{"id":"rs749381157","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569609,"source":"dbSNP","strand":1,"feature_type":"variation","end":140569609,"alleles":["T","C","G"]},{"seq_region_name":"7","id":"rs541689048","clinical_significance":[],"start":140569614,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140569614,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs768209274","source":"dbSNP","start":140569615,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","-"],"end":140569615,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs773104777","clinical_significance":[],"end":140569615,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140569615,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140569616,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569616,"source":"dbSNP","id":"rs747001028","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569618,"source":"dbSNP","strand":1,"feature_type":"variation","end":140569618,"alleles":["G","C"],"id":"rs1372761700","seq_region_name":"7","clinical_significance":[]},{"start":140569620,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140569620,"alleles":["G","A","C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1295991653","clinical_significance":[]},{"start":140569621,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140569621,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs118060470","clinical_significance":[]},{"id":"rs1359242096","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140569623,"strand":1,"feature_type":"variation","start":140569623,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140569625,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140569625,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1315141820"},{"seq_region_name":"7","id":"rs141096765","clinical_significance":[],"start":140569626,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140569626,"alleles":["C","G","T"],"strand":1,"feature_type":"variation"},{"end":140569627,"alleles":["T","C","G"],"strand":1,"feature_type":"variation","start":140569627,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs764812632","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140569629,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140569629,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1245713514"},{"alleles":["T","A"],"end":140569630,"feature_type":"variation","strand":1,"source":"dbSNP","start":140569630,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798008448"},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140569631,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569631,"clinical_significance":[],"seq_region_name":"7","id":"rs775273699"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569632,"feature_type":"variation","strand":1,"end":140569632,"alleles":["G","T"],"clinical_significance":[],"id":"rs762546035","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1203104922","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140569634,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569634,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs763736427","feature_type":"variation","strand":1,"end":140569635,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569635},{"seq_region_name":"7","id":"rs1585656418","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140569639,"assembly_name":"GRCh38","consequence_type":"splice_donor_region_variant","start":140569639,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1480047590","seq_region_name":"7","end":140569648,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140569648,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585656440","source":"dbSNP","start":140569650,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140569650,"feature_type":"variation","strand":1},{"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569652,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140569652,"clinical_significance":[],"seq_region_name":"7","id":"rs946858070"},{"end":140569653,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140569653,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs752090246"},{"end":140569655,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140569655,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","id":"rs1798009627","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","C"],"end":140569656,"feature_type":"variation","strand":1,"source":"dbSNP","start":140569656,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798009743"},{"feature_type":"variation","strand":1,"end":140569659,"alleles":["C","T"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569659,"clinical_significance":[],"seq_region_name":"7","id":"rs1798009883"},{"seq_region_name":"7","id":"rs757860814","clinical_significance":[],"start":140569661,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","end":140569661,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1193221952","seq_region_name":"7","source":"dbSNP","start":140569673,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140569673,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140569674,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569674,"clinical_significance":[],"seq_region_name":"7","id":"rs931257864"},{"clinical_significance":[],"seq_region_name":"7","id":"rs75454320","source":"dbSNP","start":140569675,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140569675,"alleles":["A","C"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140569682,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140569682,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs2130600732","seq_region_name":"7"},{"clinical_significance":[],"id":"rs767880041","seq_region_name":"7","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569683,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140569683},{"clinical_significance":[],"seq_region_name":"7","id":"rs1162533555","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140569687,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569687},{"clinical_significance":[],"seq_region_name":"7","id":"rs750754602","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140569688,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569688},{"seq_region_name":"7","id":"rs1411430708","clinical_significance":[],"start":140569689,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140569689,"alleles":["C","A","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs756299746","clinical_significance":["uncertain significance"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140569690,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140569690},{"feature_type":"variation","strand":1,"end":140569694,"alleles":["C","T"],"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569694,"clinical_significance":[],"seq_region_name":"7","id":"rs780123355"},{"clinical_significance":[],"seq_region_name":"7","id":"rs754102168","end":140569695,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140569695,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140569697,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140569697,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1220798544"},{"clinical_significance":[],"seq_region_name":"7","id":"rs755031651","feature_type":"variation","strand":1,"end":140569702,"alleles":["T","C"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569702},{"clinical_significance":[],"id":"rs778989980","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140569704,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569704},{"start":140569705,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140569705,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1275845812","clinical_significance":["uncertain significance"]},{"seq_region_name":"7","id":"rs746913377","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140569715,"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140569715,"source":"dbSNP"},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569717,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140569717,"clinical_significance":[],"seq_region_name":"7","id":"rs1563148587"},{"id":"rs367598318","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140569721,"source":"dbSNP","strand":1,"feature_type":"variation","end":140569721,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1341970091","clinical_significance":["uncertain significance"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140569722,"source":"dbSNP","strand":1,"feature_type":"variation","end":140569722,"alleles":["T","A","C"]},{"seq_region_name":"7","id":"rs745638913","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140569728,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140569728,"source":"dbSNP"},{"start":140569729,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"stop_gained","alleles":["G","A"],"end":140569729,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1272960449","clinical_significance":[]},{"seq_region_name":"7","id":"rs1464130441","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140569732,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140569732},{"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140569733,"source":"dbSNP","strand":1,"feature_type":"variation","end":140569733,"alleles":["C","A"],"seq_region_name":"7","id":"rs769699327","clinical_significance":[]},{"clinical_significance":[],"id":"rs1171311179","seq_region_name":"7","alleles":["G","A"],"end":140569741,"feature_type":"variation","strand":1,"source":"dbSNP","start":140569741,"consequence_type":"splice_region_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140569751,"assembly_name":"GRCh38","consequence_type":"splice_polypyrimidine_tract_variant","start":140569751,"source":"dbSNP","seq_region_name":"7","id":"rs2130600921","clinical_significance":[]},{"seq_region_name":"7","id":"rs1210215572","clinical_significance":[],"alleles":["AGGAG","AG"],"end":140569755,"strand":1,"feature_type":"variation","start":140569751,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_polypyrimidine_tract_variant"},{"assembly_name":"GRCh38","consequence_type":"splice_polypyrimidine_tract_variant","start":140569753,"source":"dbSNP","strand":1,"feature_type":"variation","end":140569753,"alleles":["G","A"],"seq_region_name":"7","id":"rs775250062","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["AGAAGAA","AGAA"],"end":140569760,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569754,"source":"dbSNP","seq_region_name":"7","id":"rs1421295309","clinical_significance":[]},{"seq_region_name":"7","id":"rs762741798","clinical_significance":[],"start":140569755,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_polypyrimidine_tract_variant","end":140569755,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs768231380","clinical_significance":[],"strand":1,"feature_type":"variation","end":140569760,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569760,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs774029139","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569761,"feature_type":"variation","strand":1,"end":140569761,"alleles":["C","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs762339538","source":"dbSNP","start":140569764,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140569764,"alleles":["C","T"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140569765,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569765,"clinical_significance":[],"id":"rs767919573","seq_region_name":"7"},{"alleles":["G","A"],"end":140569767,"feature_type":"variation","strand":1,"source":"dbSNP","start":140569767,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs750994536","seq_region_name":"7"},{"seq_region_name":"7","id":"rs764923867","clinical_significance":[],"alleles":["T","G"],"end":140569768,"strand":1,"feature_type":"variation","start":140569768,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798014985","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569769,"feature_type":"variation","strand":1,"end":140569769,"alleles":["G","A"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569772,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140569772,"clinical_significance":[],"id":"rs1798015084","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140569774,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569774,"source":"dbSNP","seq_region_name":"7","id":"rs1165886479","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798015307","clinical_significance":[],"start":140569776,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140569776,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140569779,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140569779,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1180152726"},{"clinical_significance":[],"id":"rs1798015504","seq_region_name":"7","source":"dbSNP","start":140569781,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140569781,"alleles":["C","T"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140569786,"alleles":["CTCTCT","CTCT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569781,"source":"dbSNP","id":"rs773670281","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140569785,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569785,"clinical_significance":[],"id":"rs766818796","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1482980472","alleles":["G","A"],"end":140569787,"feature_type":"variation","strand":1,"source":"dbSNP","start":140569787,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569788,"source":"dbSNP","strand":1,"feature_type":"variation","end":140569788,"alleles":["T","C","G"],"seq_region_name":"7","id":"rs754014300","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs552610551","alleles":["G","A"],"end":140569790,"feature_type":"variation","strand":1,"source":"dbSNP","start":140569790,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798016245","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569798,"feature_type":"variation","strand":1,"end":140569799,"alleles":["GC","-"]},{"id":"rs1798016363","seq_region_name":"7","clinical_significance":[],"start":140569803,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140569803,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140569804,"alleles":["C","A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569804,"source":"dbSNP","seq_region_name":"7","id":"rs564141246","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798016621","source":"dbSNP","start":140569814,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140569814,"alleles":["C","G"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140569815,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569815,"clinical_significance":[],"seq_region_name":"7","id":"rs1798016724"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798016829","alleles":["C","T"],"end":140569816,"feature_type":"variation","strand":1,"source":"dbSNP","start":140569816,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140569818,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569818,"source":"dbSNP","seq_region_name":"7","id":"rs1585656979","clinical_significance":[]},{"id":"rs1316446871","seq_region_name":"7","clinical_significance":[],"start":140569820,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140569820,"alleles":["T","-"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569820,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140569820,"clinical_significance":[],"seq_region_name":"7","id":"rs1798017025"},{"strand":1,"feature_type":"variation","end":140569821,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569821,"source":"dbSNP","seq_region_name":"7","id":"rs531557801","clinical_significance":[]},{"clinical_significance":[],"id":"rs587373","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140569825,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569825},{"seq_region_name":"7","id":"rs1029141322","clinical_significance":[],"start":140569826,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140569826,"alleles":["G","A","C"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140569828,"alleles":["T","C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569828,"clinical_significance":[],"seq_region_name":"7","id":"rs868738169"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569834,"source":"dbSNP","strand":1,"feature_type":"variation","end":140569834,"alleles":["G","T"],"seq_region_name":"7","id":"rs1798017881","clinical_significance":[]},{"end":140569837,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140569837,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798017987","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798018120","end":140569840,"alleles":["GGG","GGGG"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140569838,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1798018294","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140569840,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569840,"source":"dbSNP"},{"seq_region_name":"7","id":"rs556498703","clinical_significance":[],"alleles":["G","A","C"],"end":140569845,"strand":1,"feature_type":"variation","start":140569845,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140569846,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569846,"source":"dbSNP","seq_region_name":"7","id":"rs1417652813","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798018829","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569846,"feature_type":"variation","strand":1,"end":140569856,"alleles":["GGGAGTGGGAG","GGGAG"]},{"id":"rs1011868343","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140569847,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569847,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1478406465","feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140569848,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569848},{"source":"dbSNP","start":140569850,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140569850,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798019316"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140569851,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569851,"source":"dbSNP","id":"rs1798019413","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140569852,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140569852,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1169745617","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140569853,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569853,"clinical_significance":[],"seq_region_name":"7","id":"rs1170179593"},{"alleles":["G","C"],"end":140569856,"feature_type":"variation","strand":1,"source":"dbSNP","start":140569856,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1417384898"},{"clinical_significance":[],"seq_region_name":"7","id":"rs556272101","alleles":["A","G"],"end":140569859,"feature_type":"variation","strand":1,"source":"dbSNP","start":140569859,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","A"],"end":140569860,"strand":1,"feature_type":"variation","start":140569860,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1022303916","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs967618274","clinical_significance":[],"start":140569863,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140569863,"strand":1,"feature_type":"variation"},{"alleles":["G","T"],"end":140569869,"strand":1,"feature_type":"variation","start":140569869,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs977503441","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798020977","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569870,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140569870},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130601297","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569874,"feature_type":"variation","strand":1,"end":140569874,"alleles":["A","G"]},{"clinical_significance":[],"id":"rs1162965233","seq_region_name":"7","source":"dbSNP","start":140569876,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140569876,"alleles":["G","A","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1370368817","seq_region_name":"7","alleles":["GGG","GG"],"end":140569878,"feature_type":"variation","strand":1,"source":"dbSNP","start":140569876,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1035339547","alleles":["G","A"],"end":140569880,"feature_type":"variation","strand":1,"source":"dbSNP","start":140569880,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1585657168","clinical_significance":[],"end":140569887,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140569887,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs899044137","source":"dbSNP","start":140569888,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G","T"],"end":140569888,"feature_type":"variation","strand":1},{"start":140569889,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140569889,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs536124297","seq_region_name":"7","clinical_significance":[]},{"id":"rs1798022097","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569890,"source":"dbSNP","strand":1,"feature_type":"variation","end":140569890,"alleles":["C","G"]},{"seq_region_name":"7","id":"rs1181040300","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569891,"source":"dbSNP","strand":1,"feature_type":"variation","end":140569891,"alleles":["A","-"]},{"id":"rs1237926637","seq_region_name":"7","clinical_significance":[],"alleles":["A","C","T"],"end":140569891,"strand":1,"feature_type":"variation","start":140569891,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140569892,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A","C"],"end":140569892,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585657226","clinical_significance":[]},{"seq_region_name":"7","id":"rs35641355","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569892,"source":"dbSNP","strand":1,"feature_type":"variation","end":140569903,"alleles":["TTTTTTTTTTTT","TTTTTTT","TTTTTTTTTT","TTTTTTTTTTT","TTTTTTTTTTTTT"]},{"seq_region_name":"7","id":"rs1798023234","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569893,"source":"dbSNP","strand":1,"feature_type":"variation","end":140569893,"alleles":["T","A"]},{"alleles":["T","A"],"end":140569897,"feature_type":"variation","strand":1,"source":"dbSNP","start":140569897,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1266773305","seq_region_name":"7"},{"start":140569898,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140569898,"alleles":["T","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs994633768","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1320577265","source":"dbSNP","start":140569899,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140569899,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140569900,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569900,"clinical_significance":[],"seq_region_name":"7","id":"rs1798023540"},{"seq_region_name":"7","id":"rs1312024074","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569901,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140569901},{"source":"dbSNP","start":140569903,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140569903,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1242186458"},{"clinical_significance":[],"id":"rs368180145","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569904,"feature_type":"variation","strand":1,"end":140569904,"alleles":["A","T"]},{"strand":1,"feature_type":"variation","end":140569904,"alleles":["A","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569904,"source":"dbSNP","id":"rs1340924088","seq_region_name":"7","clinical_significance":[]},{"start":140569905,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A","C"],"end":140569905,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585657333","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798024242","clinical_significance":[],"end":140569911,"alleles":["TTTTTTT","TTTTTTTT"],"strand":1,"feature_type":"variation","start":140569905,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1798024374","seq_region_name":"7","end":140569911,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140569911,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["G","A","T"],"end":140569912,"strand":1,"feature_type":"variation","start":140569912,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1387079871","clinical_significance":[]},{"start":140569915,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140569915,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1392623415","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569916,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140569916,"clinical_significance":[],"seq_region_name":"7","id":"rs1798024717"},{"alleles":["A","G"],"end":140569919,"strand":1,"feature_type":"variation","start":140569919,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs6979290","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs886373518","source":"dbSNP","start":140569924,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140569924,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs566235594","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140569925,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569925,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798025214","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569927,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140569927},{"seq_region_name":"7","id":"rs1798025331","clinical_significance":[],"start":140569928,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140569928,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140569930,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569930,"clinical_significance":[],"seq_region_name":"7","id":"rs1338112294"},{"seq_region_name":"7","id":"rs1437925277","clinical_significance":[],"alleles":["C","T"],"end":140569933,"strand":1,"feature_type":"variation","start":140569933,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1798025697","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140569934,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569934,"source":"dbSNP"},{"id":"rs545088843","seq_region_name":"7","clinical_significance":[],"start":140569937,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140569936,"alleles":["-","AGG"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569942,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140569942,"clinical_significance":[],"id":"rs1798025964","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["TG","-"],"end":140569943,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569942,"clinical_significance":[],"seq_region_name":"7","id":"rs2130601623"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140569946,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569946,"source":"dbSNP","seq_region_name":"7","id":"rs1281888607","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585657444","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569947,"feature_type":"variation","strand":1,"end":140569947,"alleles":["T","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1484471063","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569948,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140569948},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569950,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140569950,"clinical_significance":[],"seq_region_name":"7","id":"rs1008747721"},{"strand":1,"feature_type":"variation","end":140569955,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569955,"source":"dbSNP","seq_region_name":"7","id":"rs1435269686","clinical_significance":[]},{"end":140569956,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140569956,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs991231721","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1798026845","clinical_significance":[],"strand":1,"feature_type":"variation","end":140569957,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569957,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1798026952","seq_region_name":"7","source":"dbSNP","start":140569958,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140569958,"alleles":["A","G"],"feature_type":"variation","strand":1},{"alleles":["C","T"],"end":140569963,"strand":1,"feature_type":"variation","start":140569963,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798027069","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs767677459","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140569969,"feature_type":"variation","strand":1,"end":140569969,"alleles":["A","C"]},{"end":140569977,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140569977,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798027291","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140569979,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140569979,"source":"dbSNP","id":"rs1798027415","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1490095689","end":140569983,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140569983,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140569987,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140569987,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs773144325","clinical_significance":[]},{"source":"dbSNP","start":140569991,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140569991,"alleles":["T","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1488824189","seq_region_name":"7"},{"alleles":["A","C"],"end":140569994,"strand":1,"feature_type":"variation","start":140569994,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1798027882","seq_region_name":"7","clinical_significance":[]},{"end":140570002,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140570002,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs975265048","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570005,"feature_type":"variation","strand":1,"end":140570005,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1195879251"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585657568","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140570009,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570009},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563148808","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570012,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140570012},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570014,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140570014,"seq_region_name":"7","id":"rs1798028447","clinical_significance":[]},{"alleles":["G","A"],"end":140570022,"strand":1,"feature_type":"variation","start":140570022,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1278816651","clinical_significance":[]},{"alleles":["T","A"],"end":140570023,"strand":1,"feature_type":"variation","start":140570023,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1233965877","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs952660564","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140570028,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570028},{"source":"dbSNP","start":140570029,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140570029,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798028917"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140570030,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570030,"clinical_significance":[],"seq_region_name":"7","id":"rs1022373798"},{"source":"dbSNP","start":140570035,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140570035,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798029142"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1298990484","alleles":["G","C"],"end":140570037,"feature_type":"variation","strand":1,"source":"dbSNP","start":140570037,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1475413946","clinical_significance":[],"alleles":["C","G"],"end":140570041,"strand":1,"feature_type":"variation","start":140570041,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140570043,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140570043,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798029514"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798029650","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140570045,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570045},{"source":"dbSNP","start":140570046,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140570046,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1173204865","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570048,"feature_type":"variation","strand":1,"end":140570048,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1798029928"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798030057","source":"dbSNP","start":140570052,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140570052,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1386398665","end":140570058,"alleles":["C","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140570058,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140570059,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C","G"],"end":140570059,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1361370951"},{"seq_region_name":"7","id":"rs192073979","clinical_significance":[],"alleles":["A","T"],"end":140570061,"strand":1,"feature_type":"variation","start":140570061,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs908473887","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570062,"source":"dbSNP","strand":1,"feature_type":"variation","end":140570062,"alleles":["T","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs939926062","alleles":["T","C","G"],"end":140570070,"feature_type":"variation","strand":1,"source":"dbSNP","start":140570070,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1798030762","clinical_significance":[],"alleles":["T","A"],"end":140570074,"strand":1,"feature_type":"variation","start":140570074,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1173656877","clinical_significance":[],"end":140570076,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140570076,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1585657690","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570078,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140570078},{"source":"dbSNP","start":140570083,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140570083,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs182754722"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570084,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140570084,"seq_region_name":"7","id":"rs683691","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1360859981","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140570086,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570086},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798031540","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570089,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140570089},{"source":"dbSNP","start":140570092,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C","G"],"end":140570092,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs992409672"},{"seq_region_name":"7","id":"rs1798031771","clinical_significance":[],"alleles":["C","T"],"end":140570093,"strand":1,"feature_type":"variation","start":140570093,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs2130602023","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570096,"feature_type":"variation","strand":1,"end":140570096,"alleles":["C","T"]},{"id":"rs2130602030","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570097,"source":"dbSNP","strand":1,"feature_type":"variation","end":140570097,"alleles":["A","G"]},{"source":"dbSNP","start":140570102,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140570102,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798031891"},{"id":"rs1263385146","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140570109,"strand":1,"feature_type":"variation","start":140570109,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140570110,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140570110,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs916935843","clinical_significance":[]},{"end":140570111,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140570111,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585657750"},{"clinical_significance":[],"seq_region_name":"7","id":"rs948412246","feature_type":"variation","strand":1,"end":140570114,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570114},{"seq_region_name":"7","id":"rs1044415775","clinical_significance":[],"start":140570115,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140570115,"strand":1,"feature_type":"variation"},{"alleles":["C","T"],"end":140570118,"feature_type":"variation","strand":1,"source":"dbSNP","start":140570118,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798032630"},{"end":140570119,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140570119,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1200945624"},{"source":"dbSNP","start":140570120,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140570120,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1347092712"},{"seq_region_name":"7","id":"rs1316040236","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140570125,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570125,"source":"dbSNP"},{"start":140570129,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140570129,"alleles":["A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585657809","clinical_significance":[]},{"id":"rs933448606","seq_region_name":"7","clinical_significance":[],"start":140570130,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140570130,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140570131,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570131,"source":"dbSNP","id":"rs1050464614","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570132,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140570132,"clinical_significance":[],"id":"rs1222610425","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs930368259","source":"dbSNP","start":140570138,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140570138,"alleles":["A","C","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1280327949","source":"dbSNP","start":140570139,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140570139,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1437163772","clinical_significance":[],"start":140570141,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140570141,"alleles":["C","G","T"],"strand":1,"feature_type":"variation"},{"end":140570142,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140570142,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs488706"},{"strand":1,"feature_type":"variation","end":140570144,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570144,"source":"dbSNP","id":"rs1334977489","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1397889533","source":"dbSNP","start":140570147,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140570147,"alleles":["G","A"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140570155,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140570155,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1345156704"},{"seq_region_name":"7","id":"rs886257263","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140570159,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570159,"source":"dbSNP"},{"alleles":["G","C","T"],"end":140570160,"feature_type":"variation","strand":1,"source":"dbSNP","start":140570160,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1012163644"},{"seq_region_name":"7","id":"rs1043200725","clinical_significance":[],"start":140570165,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140570165,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"end":140570169,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140570169,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798034796"},{"end":140570171,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140570171,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs537890064","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140570172,"alleles":["G","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570172,"clinical_significance":[],"seq_region_name":"7","id":"rs1172357951"},{"source":"dbSNP","start":140570173,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140570173,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798035219"},{"end":140570174,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140570174,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs999097306"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140570175,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570175,"source":"dbSNP","id":"rs113174788","seq_region_name":"7","clinical_significance":[]},{"start":140570176,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140570176,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs561386689","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570177,"feature_type":"variation","strand":1,"end":140570177,"alleles":["G","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1022682534"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140570183,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570183,"source":"dbSNP","seq_region_name":"7","id":"rs116968651","clinical_significance":[]},{"clinical_significance":[],"id":"rs978147969","seq_region_name":"7","end":140570184,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140570184,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1259805532","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570185,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140570185},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798036160","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570187,"feature_type":"variation","strand":1,"end":140570187,"alleles":["A","T"]},{"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140570188,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570188,"source":"dbSNP","seq_region_name":"7","id":"rs1216997688","clinical_significance":[]},{"seq_region_name":"7","id":"rs1338936185","clinical_significance":[],"alleles":["A","G"],"end":140570196,"strand":1,"feature_type":"variation","start":140570196,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs113260266","end":140570200,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140570200,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140570205,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140570205,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1450231241","clinical_significance":[]},{"source":"dbSNP","start":140570207,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140570207,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1798036798","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140570221,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570221,"clinical_significance":[],"seq_region_name":"7","id":"rs952471311"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570222,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140570222,"clinical_significance":[],"seq_region_name":"7","id":"rs1455573837"},{"clinical_significance":[],"seq_region_name":"7","id":"rs572157842","end":140570223,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140570223,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1798037309","clinical_significance":[],"start":140570229,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140570229,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570237,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140570237,"seq_region_name":"7","id":"rs1383995638","clinical_significance":[]},{"start":140570238,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140570238,"alleles":["A","G"],"strand":1,"feature_type":"variation","id":"rs992860440","seq_region_name":"7","clinical_significance":[]},{"start":140570239,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140570239,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1402886007","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570240,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140570240,"seq_region_name":"7","id":"rs1798037684","clinical_significance":[]},{"source":"dbSNP","start":140570247,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140570251,"alleles":["GGCTG","GGCTGGCTG"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798037776"},{"seq_region_name":"7","id":"rs1329785800","clinical_significance":[],"end":140570255,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140570255,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs908359512","clinical_significance":[],"end":140570256,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140570256,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["C","T"],"end":140570258,"feature_type":"variation","strand":1,"source":"dbSNP","start":140570258,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1418295501"},{"feature_type":"variation","strand":1,"end":140570261,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570261,"clinical_significance":[],"seq_region_name":"7","id":"rs207468671"},{"id":"rs961614853","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140570262,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570262,"source":"dbSNP"},{"start":140570265,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140570265,"alleles":["C","G"],"strand":1,"feature_type":"variation","id":"rs1585658207","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570268,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140570268,"clinical_significance":[],"seq_region_name":"7","id":"rs112743805"},{"clinical_significance":[],"id":"rs2130602503","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570271,"feature_type":"variation","strand":1,"end":140570271,"alleles":["G","A"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570273,"feature_type":"variation","strand":1,"end":140570273,"alleles":["C","T"],"clinical_significance":[],"id":"rs755404946","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140570274,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570274,"source":"dbSNP","seq_region_name":"7","id":"rs6957365","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798038987","source":"dbSNP","start":140570279,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140570279,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs2130602538","clinical_significance":[],"start":140570287,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140570287,"strand":1,"feature_type":"variation"},{"id":"rs1798039099","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140570289,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570289,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570296,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140570296,"clinical_significance":[],"seq_region_name":"7","id":"rs531688683"},{"alleles":["G","A","C"],"end":140570297,"strand":1,"feature_type":"variation","start":140570297,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1050348989","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570300,"feature_type":"variation","strand":1,"end":140570300,"alleles":["C","G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1309435641"},{"source":"dbSNP","start":140570301,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140570301,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798039519"},{"clinical_significance":[],"seq_region_name":"7","id":"rs549790499","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570305,"feature_type":"variation","strand":1,"end":140570305,"alleles":["G","A"]},{"start":140570308,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140570308,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs561731032","clinical_significance":[]},{"end":140570312,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140570312,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs746017662","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798039953","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570313,"source":"dbSNP","strand":1,"feature_type":"variation","end":140570313,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs74390720","end":140570314,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140570314,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1196471014","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140570316,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570316,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1259281449","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140570321,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570321,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570322,"feature_type":"variation","strand":1,"end":140570322,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1290778099"},{"source":"dbSNP","start":140570322,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","AA"],"end":140570322,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798040589"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570324,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140570324,"seq_region_name":"7","id":"rs1350447125","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570327,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140570327,"clinical_significance":[],"seq_region_name":"7","id":"rs1798040823"},{"seq_region_name":"7","id":"rs1230314322","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570328,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140570328},{"feature_type":"variation","strand":1,"end":140570333,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570333,"clinical_significance":[],"seq_region_name":"7","id":"rs1798041042"},{"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140570334,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570334,"clinical_significance":[],"seq_region_name":"7","id":"rs1798041153"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798041256","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140570335,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570335},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570337,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140570337,"clinical_significance":[],"seq_region_name":"7","id":"rs947479341"},{"seq_region_name":"7","id":"rs1798041381","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570339,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140570339},{"seq_region_name":"7","id":"rs548023586","clinical_significance":[],"start":140570340,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140570340,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1314520182","clinical_significance":[],"start":140570341,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140570341,"alleles":["G","A","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798041751","alleles":["A","C"],"end":140570342,"feature_type":"variation","strand":1,"source":"dbSNP","start":140570342,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140570348,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140570348,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs768628188"},{"clinical_significance":[],"id":"rs1241471795","seq_region_name":"7","feature_type":"variation","strand":1,"end":140570349,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570349},{"end":140570353,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140570353,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798042076"},{"clinical_significance":[],"id":"rs1379715235","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570355,"feature_type":"variation","strand":1,"end":140570355,"alleles":["C","T"]},{"end":140570356,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140570356,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs144605900"},{"source":"dbSNP","start":140570359,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140570359,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1047454749"},{"source":"dbSNP","start":140570362,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140570362,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798042532"},{"start":140570364,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140570364,"strand":1,"feature_type":"variation","id":"rs1798042642","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570365,"feature_type":"variation","strand":1,"end":140570365,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs907744656"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570366,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140570366,"clinical_significance":[],"seq_region_name":"7","id":"rs944551921"},{"feature_type":"variation","strand":1,"end":140570367,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570367,"clinical_significance":[],"seq_region_name":"7","id":"rs999140278"},{"source":"dbSNP","start":140570374,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140570374,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs187517410"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1421051385","source":"dbSNP","start":140570377,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140570377,"feature_type":"variation","strand":1},{"end":140570378,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140570378,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1439795105"},{"seq_region_name":"7","id":"rs1798043534","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570384,"source":"dbSNP","strand":1,"feature_type":"variation","end":140570384,"alleles":["G","A"]},{"end":140570386,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140570386,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585658524","clinical_significance":[]},{"start":140570391,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140570391,"strand":1,"feature_type":"variation","id":"rs1678350161","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs900423130","clinical_significance":[],"end":140570392,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140570392,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs2130602884","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570394,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140570394},{"seq_region_name":"7","id":"rs1179960486","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140570400,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570400,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1469435317","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570401,"feature_type":"variation","strand":1,"end":140570401,"alleles":["C","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570402,"feature_type":"variation","strand":1,"end":140570402,"alleles":["C","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1798044151"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1247127826","feature_type":"variation","strand":1,"alleles":["CAAAACAAAACAA","CAAAACAA"],"end":140570414,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570402},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570407,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140570407,"seq_region_name":"7","id":"rs1798044391","clinical_significance":[]},{"alleles":["A","T"],"end":140570409,"feature_type":"variation","strand":1,"source":"dbSNP","start":140570409,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798044520"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570411,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140570411,"id":"rs1798044623","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs896030817","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570413,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140570413},{"clinical_significance":[],"id":"rs1362940382","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140570424,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570424},{"clinical_significance":[],"id":"rs58590331","seq_region_name":"7","end":140570426,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140570426,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1291363255","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570431,"feature_type":"variation","strand":1,"end":140570439,"alleles":["AAAAAAAAA","AAAAAAAA","AAAAAAAAAA"]},{"strand":1,"feature_type":"variation","end":140570434,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570434,"source":"dbSNP","seq_region_name":"7","id":"rs1798045312","clinical_significance":[]},{"seq_region_name":"7","id":"rs1392195112","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140570437,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570437,"source":"dbSNP"},{"source":"dbSNP","start":140570439,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140570439,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798045536"},{"seq_region_name":"7","id":"rs1043764515","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140570440,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570440,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570440,"feature_type":"variation","strand":1,"alleles":["G","-"],"end":140570440,"clinical_significance":[],"id":"rs1798045787","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1331413474","alleles":["T","C"],"end":140570442,"feature_type":"variation","strand":1,"source":"dbSNP","start":140570442,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140570445,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140570445,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798046007","clinical_significance":[]},{"end":140570451,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140570451,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798046126","clinical_significance":[]},{"seq_region_name":"7","id":"rs376969112","clinical_significance":[],"start":140570454,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140570454,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs999645515","end":140570457,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140570457,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs570591432","feature_type":"variation","strand":1,"end":140570461,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570461},{"seq_region_name":"7","id":"rs1005283714","clinical_significance":[],"end":140570462,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140570462,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs537927122","clinical_significance":[],"start":140570463,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140570463,"strand":1,"feature_type":"variation"},{"end":140570466,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140570466,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1015882629","clinical_significance":[]},{"clinical_significance":[],"id":"rs1798046926","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570468,"feature_type":"variation","strand":1,"end":140570468,"alleles":["A","C"]},{"strand":1,"feature_type":"variation","end":140570470,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570470,"source":"dbSNP","seq_region_name":"7","id":"rs681892","clinical_significance":[]},{"id":"rs1302160125","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570474,"source":"dbSNP","strand":1,"feature_type":"variation","end":140570474,"alleles":["C","T"]},{"clinical_significance":[],"id":"rs867401226","seq_region_name":"7","source":"dbSNP","start":140570476,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140570476,"alleles":["A","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798047503","feature_type":"variation","strand":1,"end":140570477,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570477},{"end":140570478,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140570478,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs568017910"},{"seq_region_name":"7","id":"rs974714665","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140570479,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570479,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs566676611","alleles":["T","C"],"end":140570482,"feature_type":"variation","strand":1,"source":"dbSNP","start":140570482,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1425569876","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140570483,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570483,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1798048143","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570484,"source":"dbSNP","strand":1,"feature_type":"variation","end":140570484,"alleles":["T","C"]},{"clinical_significance":[],"id":"rs535386475","seq_region_name":"7","alleles":["G","T"],"end":140570487,"feature_type":"variation","strand":1,"source":"dbSNP","start":140570487,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs76103843","source":"dbSNP","start":140570496,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140570496,"alleles":["T","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1268381952","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140570499,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570499,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570500,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140570500,"seq_region_name":"7","id":"rs983201045","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs953942532","source":"dbSNP","start":140570501,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140570501,"alleles":["G","C","T"],"feature_type":"variation","strand":1},{"end":140570503,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140570503,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798048975"},{"end":140570504,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140570504,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1250066468","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140570506,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570506,"clinical_significance":[],"seq_region_name":"7","id":"rs1798049204"},{"end":140570507,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140570507,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1681789","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570508,"feature_type":"variation","strand":1,"end":140570508,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1313254687"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1040219365","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570509,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140570509},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140570511,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570511,"source":"dbSNP","seq_region_name":"7","id":"rs56370096","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570512,"source":"dbSNP","strand":1,"feature_type":"variation","end":140570512,"alleles":["C","A","T"],"id":"rs910533789","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs931940592","clinical_significance":[],"alleles":["G","A"],"end":140570513,"strand":1,"feature_type":"variation","start":140570513,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1639985","clinical_significance":[],"start":140570518,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140570518,"strand":1,"feature_type":"variation"},{"start":140570520,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140570520,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1341813423","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140570523,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570523,"source":"dbSNP","seq_region_name":"7","id":"rs1171337650","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570527,"feature_type":"variation","strand":1,"end":140570527,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs576163997"},{"clinical_significance":[],"seq_region_name":"7","id":"rs6972562","feature_type":"variation","strand":1,"end":140570530,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570530},{"alleles":["G","A","C"],"end":140570531,"feature_type":"variation","strand":1,"source":"dbSNP","start":140570531,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1359627793"},{"alleles":["A","G"],"end":140570532,"feature_type":"variation","strand":1,"source":"dbSNP","start":140570532,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1798050874","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570533,"source":"dbSNP","strand":1,"feature_type":"variation","end":140570533,"alleles":["G","C"],"seq_region_name":"7","id":"rs1467980676","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140570536,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570536,"source":"dbSNP","seq_region_name":"7","id":"rs924656170","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570540,"feature_type":"variation","strand":1,"end":140570540,"alleles":["C","A","G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs934818187"},{"seq_region_name":"7","id":"rs1478946676","clinical_significance":[],"end":140570545,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140570545,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570548,"source":"dbSNP","strand":1,"feature_type":"variation","end":140570548,"alleles":["T","A"],"seq_region_name":"7","id":"rs1259948223","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570549,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140570549,"clinical_significance":[],"seq_region_name":"7","id":"rs1297164707"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1057296825","source":"dbSNP","start":140570550,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140570550,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs896082880","source":"dbSNP","start":140570551,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140570551,"alleles":["G","A"],"feature_type":"variation","strand":1},{"alleles":["G","A"],"end":140570553,"feature_type":"variation","strand":1,"source":"dbSNP","start":140570553,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1798051888","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798052017","source":"dbSNP","start":140570556,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140570556,"alleles":["G","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs948938445","source":"dbSNP","start":140570558,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140570558,"alleles":["G","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798052218","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570559,"feature_type":"variation","strand":1,"end":140570559,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1208723430","clinical_significance":[],"start":140570563,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140570563,"alleles":["C","A","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798052459","end":140570564,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140570564,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140570571,"alleles":["C","A","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570571,"clinical_significance":[],"seq_region_name":"7","id":"rs1249533929"},{"end":140570572,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140570572,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1218830201"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570574,"source":"dbSNP","strand":1,"feature_type":"variation","end":140570574,"alleles":["G","A"],"seq_region_name":"7","id":"rs1319513949","clinical_significance":[]},{"alleles":["C","T"],"end":140570575,"strand":1,"feature_type":"variation","start":140570575,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs116236478","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140570576,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570576,"source":"dbSNP","seq_region_name":"7","id":"rs888117725","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798053065","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570587,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140570587},{"start":140570588,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140570588,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs538138906","clinical_significance":[]},{"id":"rs1798053333","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140570595,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570595,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570597,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140570597,"clinical_significance":[],"seq_region_name":"7","id":"rs1798053419"},{"clinical_significance":[],"seq_region_name":"7","id":"rs775236138","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570600,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140570600},{"seq_region_name":"7","id":"rs1015353305","clinical_significance":[],"strand":1,"feature_type":"variation","end":140570601,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570601,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798053777","feature_type":"variation","strand":1,"end":140570603,"alleles":["CGC","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570601},{"feature_type":"variation","strand":1,"end":140570602,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570602,"clinical_significance":[],"id":"rs556323554","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570604,"feature_type":"variation","strand":1,"end":140570604,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1233134633"},{"start":140570607,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140570607,"strand":1,"feature_type":"variation","id":"rs1331738759","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1023831310","seq_region_name":"7","alleles":["G","A"],"end":140570610,"feature_type":"variation","strand":1,"source":"dbSNP","start":140570610,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140570612,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570612,"source":"dbSNP","seq_region_name":"7","id":"rs112275951","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798054556","source":"dbSNP","start":140570613,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140570613,"alleles":["G","A"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570615,"feature_type":"variation","strand":1,"end":140570615,"alleles":["C","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs753100767"},{"start":140570616,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140570616,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798054833","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140570620,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570620,"clinical_significance":[],"id":"rs1416127105","seq_region_name":"7"},{"alleles":["C","A"],"end":140570622,"strand":1,"feature_type":"variation","start":140570622,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1029423683","clinical_significance":[]},{"id":"rs953986340","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570631,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140570631},{"start":140570632,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140570632,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1239355249","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798055423","clinical_significance":[],"start":140570643,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140570643,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"alleles":["A","G"],"end":140570644,"feature_type":"variation","strand":1,"source":"dbSNP","start":140570644,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs2130603711","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1798055522","clinical_significance":[],"end":140570648,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140570648,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140570649,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140570649,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs756662371","clinical_significance":[]},{"seq_region_name":"7","id":"rs577572880","clinical_significance":[],"start":140570650,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140570650,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs985339230","feature_type":"variation","strand":1,"alleles":["T","A"],"end":140570654,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570654},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140570661,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570661,"source":"dbSNP","seq_region_name":"7","id":"rs1203466436","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570663,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140570663,"clinical_significance":[],"seq_region_name":"7","id":"rs1798056042"},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140570664,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570664,"clinical_significance":[],"seq_region_name":"7","id":"rs1321767787"},{"clinical_significance":[],"id":"rs1798056273","seq_region_name":"7","end":140570666,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140570666,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570668,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140570668,"seq_region_name":"7","id":"rs1798056373","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570670,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140570670,"id":"rs1314293081","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585659343","clinical_significance":[],"alleles":["A","C"],"end":140570673,"strand":1,"feature_type":"variation","start":140570673,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570674,"feature_type":"variation","strand":1,"end":140570676,"alleles":["CCC","CC"],"clinical_significance":[],"seq_region_name":"7","id":"rs550253579"},{"end":140570675,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140570675,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1255088265","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798056961","end":140570677,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140570677,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140570681,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140570681,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs951591651","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798057176","end":140570684,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140570684,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140570690,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570690,"clinical_significance":[],"seq_region_name":"7","id":"rs562176032"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570692,"feature_type":"variation","strand":1,"end":140570692,"alleles":["C","A"],"clinical_significance":[],"id":"rs1018054202","seq_region_name":"7"},{"source":"dbSNP","start":140570695,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140570695,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1394150603"},{"source":"dbSNP","start":140570698,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140570698,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs138559502"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570699,"feature_type":"variation","strand":1,"end":140570699,"alleles":["C","A"],"clinical_significance":[],"id":"rs1798057648","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140570700,"alleles":["T","TGGAT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570700,"clinical_significance":[],"id":"rs1393257471","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140570701,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570701,"clinical_significance":[],"seq_region_name":"7","id":"rs979132093"},{"end":140570704,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140570704,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs976218205","clinical_significance":[]},{"clinical_significance":[],"id":"rs1798058137","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570705,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140570705},{"end":140570709,"alleles":["GG","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140570708,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798058247"},{"start":140570709,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140570709,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1444109051","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140570710,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570710,"clinical_significance":[],"seq_region_name":"7","id":"rs1798058501"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798058604","alleles":["C","T"],"end":140570711,"feature_type":"variation","strand":1,"source":"dbSNP","start":140570711,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140570715,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140570715,"alleles":["C","G"],"strand":1,"feature_type":"variation","id":"rs2130603942","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs754202513","end":140570721,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140570721,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140570722,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140570722,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130603969"},{"id":"rs1798058715","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570725,"source":"dbSNP","strand":1,"feature_type":"variation","end":140570725,"alleles":["G","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585659500","source":"dbSNP","start":140570729,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140570729,"alleles":["T","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1453738170","clinical_significance":[],"start":140570733,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140570733,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs552040047","feature_type":"variation","strand":1,"alleles":["C","A","G"],"end":140570734,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570734},{"seq_region_name":"7","id":"rs1417704236","clinical_significance":[],"strand":1,"feature_type":"variation","end":140570739,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570739,"source":"dbSNP"},{"end":140570743,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140570743,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs931805223","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs924737561","source":"dbSNP","start":140570748,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140570748,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs934702180","end":140570750,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140570750,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140570751,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570751,"clinical_significance":[],"seq_region_name":"7","id":"rs993023913"},{"clinical_significance":[],"seq_region_name":"7","id":"rs917404595","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570756,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140570756},{"id":"rs1219543404","seq_region_name":"7","clinical_significance":[],"end":140570759,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140570759,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1169100623","clinical_significance":[],"start":140570761,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140570761,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140570765,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570765,"source":"dbSNP","seq_region_name":"7","id":"rs1798060231","clinical_significance":[]},{"clinical_significance":[],"id":"rs376133487","seq_region_name":"7","alleles":["C","T"],"end":140570767,"feature_type":"variation","strand":1,"source":"dbSNP","start":140570767,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1286643558","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570773,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140570773},{"alleles":["C","T"],"end":140570775,"strand":1,"feature_type":"variation","start":140570775,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1242299975","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140570776,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570776,"source":"dbSNP","seq_region_name":"7","id":"rs1798060732","clinical_significance":[]},{"id":"rs570231584","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140570777,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570777,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1333746034","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570791,"source":"dbSNP","strand":1,"feature_type":"variation","end":140570791,"alleles":["G","C"]},{"id":"rs1798061114","seq_region_name":"7","clinical_significance":[],"end":140570792,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140570792,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs979221517","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570796,"source":"dbSNP","strand":1,"feature_type":"variation","end":140570796,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1798061359","clinical_significance":[],"start":140570799,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140570799,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570800,"source":"dbSNP","strand":1,"feature_type":"variation","end":140570800,"alleles":["T","A","C"],"seq_region_name":"7","id":"rs1387169843","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798061748","source":"dbSNP","start":140570802,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140570802,"alleles":["C","A","T"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570805,"source":"dbSNP","strand":1,"feature_type":"variation","end":140570805,"alleles":["T","C"],"seq_region_name":"7","id":"rs1798061995","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798062169","clinical_significance":[],"start":140570806,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140570806,"alleles":["T","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798062297","feature_type":"variation","strand":1,"alleles":["A","T"],"end":140570810,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570810},{"source":"dbSNP","start":140570811,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140570811,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1369941319"},{"feature_type":"variation","strand":1,"end":140570812,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570812,"clinical_significance":[],"seq_region_name":"7","id":"rs1798062536"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570815,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140570815,"clinical_significance":[],"seq_region_name":"7","id":"rs1395180303"},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140570817,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570817,"source":"dbSNP","id":"rs1585659710","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140570819,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570819,"source":"dbSNP","id":"rs192750031","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1044645211","seq_region_name":"7","feature_type":"variation","strand":1,"end":140570825,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570825},{"seq_region_name":"7","id":"rs1798063025","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570826,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140570826},{"clinical_significance":[],"seq_region_name":"7","id":"rs757469139","end":140570827,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140570827,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570829,"source":"dbSNP","strand":1,"feature_type":"variation","end":140570829,"alleles":["A","G"],"seq_region_name":"7","id":"rs1798063289","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs549853199","alleles":["A","G"],"end":140570832,"feature_type":"variation","strand":1,"source":"dbSNP","start":140570832,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570833,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140570833,"clinical_significance":[],"seq_region_name":"7","id":"rs1798063568"},{"start":140570835,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140570835,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1160963452","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1037082962","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570838,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140570838},{"seq_region_name":"7","id":"rs1798064162","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140570839,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570839,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570843,"source":"dbSNP","strand":1,"feature_type":"variation","end":140570843,"alleles":["A","C"],"id":"rs2130604302","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","T"],"end":140570848,"strand":1,"feature_type":"variation","start":140570848,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1363754524","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1199962161","feature_type":"variation","strand":1,"end":140570855,"alleles":["ACCAAA","ACCAAACACCAAA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570850},{"seq_region_name":"7","id":"rs1798064922","clinical_significance":[],"start":140570853,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140570853,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs145123287","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["AAAAAA","AAAAA"],"end":140570858,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570853,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570856,"source":"dbSNP","strand":1,"feature_type":"variation","end":140570856,"alleles":["A","G"],"id":"rs1798065296","seq_region_name":"7","clinical_significance":[]},{"id":"rs1798065463","seq_region_name":"7","clinical_significance":[],"alleles":["A","C"],"end":140570857,"strand":1,"feature_type":"variation","start":140570857,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1798065656","seq_region_name":"7","clinical_significance":[],"start":140570859,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140570859,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"id":"rs779166301","seq_region_name":"7","clinical_significance":[],"end":140570861,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140570861,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798065972","source":"dbSNP","start":140570863,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140570863,"feature_type":"variation","strand":1},{"start":140570863,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["GG","GGGG"],"end":140570864,"strand":1,"feature_type":"variation","id":"rs1585659832","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570864,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140570864,"seq_region_name":"7","id":"rs1798066188","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs896924160","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570865,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140570865},{"alleles":["C","T"],"end":140570870,"feature_type":"variation","strand":1,"source":"dbSNP","start":140570870,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1196921819"},{"seq_region_name":"7","id":"rs1798066391","clinical_significance":[],"alleles":["T","C"],"end":140570872,"strand":1,"feature_type":"variation","start":140570872,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140570874,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C","G"],"end":140570874,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs997870913"},{"strand":1,"feature_type":"variation","end":140570881,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570881,"source":"dbSNP","seq_region_name":"7","id":"rs1798066666","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585659881","clinical_significance":[],"alleles":["T","C"],"end":140570884,"strand":1,"feature_type":"variation","start":140570884,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1263332654","alleles":["C","G"],"end":140570888,"feature_type":"variation","strand":1,"source":"dbSNP","start":140570888,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1206791076","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570889,"feature_type":"variation","strand":1,"alleles":["TCTTCTT","TCTT"],"end":140570895},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570891,"feature_type":"variation","strand":1,"end":140570891,"alleles":["T","C"],"clinical_significance":[],"id":"rs1348406291","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570895,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140570895,"id":"rs1798067217","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","A","T"],"end":140570897,"strand":1,"feature_type":"variation","start":140570897,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1173013602","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140570898,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570898,"source":"dbSNP","seq_region_name":"7","id":"rs745930584","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1233631245","end":140570906,"alleles":["C","A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140570906,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140570909,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570909,"clinical_significance":[],"seq_region_name":"7","id":"rs7795017"},{"seq_region_name":"7","id":"rs1007099624","clinical_significance":[],"end":140570911,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140570911,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140570916,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570916,"source":"dbSNP","seq_region_name":"7","id":"rs141681234","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140570917,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570917,"source":"dbSNP","seq_region_name":"7","id":"rs905397148","clinical_significance":[]},{"source":"dbSNP","start":140570918,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140570918,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1341190672","seq_region_name":"7"},{"id":"rs2130604546","seq_region_name":"7","clinical_significance":[],"end":140570925,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140570925,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1798068192","clinical_significance":[],"strand":1,"feature_type":"variation","end":140570931,"alleles":["TTTT","TTT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570928,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140570935,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570935,"clinical_significance":[],"id":"rs1798068294","seq_region_name":"7"},{"source":"dbSNP","start":140570937,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140570937,"alleles":["G","C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1278475336"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798068527","feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140570944,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570944},{"seq_region_name":"7","id":"rs1380623220","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570944,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CCCCC","CCCC"],"end":140570948},{"alleles":["C","T"],"end":140570946,"feature_type":"variation","strand":1,"source":"dbSNP","start":140570946,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1384799710","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs968345734","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570947,"feature_type":"variation","strand":1,"end":140570947,"alleles":["C","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570948,"source":"dbSNP","strand":1,"feature_type":"variation","end":140570948,"alleles":["C","T"],"id":"rs2130604596","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798069108","source":"dbSNP","start":140570950,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140570950,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1798069200","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570951,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140570951},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798069292","source":"dbSNP","start":140570956,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140570956,"alleles":["G","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1798069402","clinical_significance":[],"alleles":["G","A"],"end":140570965,"strand":1,"feature_type":"variation","start":140570965,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798069510","feature_type":"variation","strand":1,"end":140570968,"alleles":["T","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570968},{"clinical_significance":[],"id":"rs1798069640","seq_region_name":"7","feature_type":"variation","strand":1,"end":140570970,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570970},{"strand":1,"feature_type":"variation","end":140570972,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570972,"source":"dbSNP","seq_region_name":"7","id":"rs679600","clinical_significance":[]},{"alleles":["G","A","T"],"end":140570973,"strand":1,"feature_type":"variation","start":140570973,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1027074945","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570974,"feature_type":"variation","strand":1,"end":140570974,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130604693"},{"start":140570976,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140570976,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798070130","clinical_significance":[]},{"source":"dbSNP","start":140570977,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140570977,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130604706"},{"alleles":["T","C"],"end":140570978,"feature_type":"variation","strand":1,"source":"dbSNP","start":140570978,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs887372455"},{"id":"rs1032076310","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140570980,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570980,"source":"dbSNP"},{"source":"dbSNP","start":140570981,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140570981,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1427707185"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570982,"feature_type":"variation","strand":1,"end":140570982,"alleles":["A","C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1173786893"},{"clinical_significance":[],"id":"rs1798070921","seq_region_name":"7","source":"dbSNP","start":140570986,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140570986,"alleles":["G","A"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140570990,"source":"dbSNP","strand":1,"feature_type":"variation","end":140570990,"alleles":["T","C"],"seq_region_name":"7","id":"rs956132947","clinical_significance":[]},{"start":140570998,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140570998,"strand":1,"feature_type":"variation","id":"rs1798071123","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798071234","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140570999,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140570999},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130604776","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140571000,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571000},{"end":140571004,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140571004,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs992911002","seq_region_name":"7","clinical_significance":[]},{"id":"rs917456868","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140571005,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571005,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571010,"source":"dbSNP","strand":1,"feature_type":"variation","end":140571010,"alleles":["G","A"],"id":"rs1798071572","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1262316192","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140571011,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571011},{"strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140571013,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571013,"source":"dbSNP","id":"rs747987013","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140571014,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571014,"clinical_significance":[],"id":"rs1014614873","seq_region_name":"7"},{"id":"rs1444794058","seq_region_name":"7","clinical_significance":[],"start":140571019,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140571019,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1260878905","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571021,"source":"dbSNP","strand":1,"feature_type":"variation","end":140571021,"alleles":["A","G"]},{"alleles":["TTAGTT","TT"],"end":140571027,"strand":1,"feature_type":"variation","start":140571022,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs759517092","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571024,"source":"dbSNP","strand":1,"feature_type":"variation","end":140571024,"alleles":["A","C","T"],"seq_region_name":"7","id":"rs1484842249","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140571024,"alleles":["A","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571024,"clinical_significance":[],"id":"rs1798072464","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571025,"source":"dbSNP","strand":1,"feature_type":"variation","end":140571025,"alleles":["G","C"],"seq_region_name":"7","id":"rs966086087","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571029,"source":"dbSNP","strand":1,"feature_type":"variation","end":140571029,"alleles":["T","C"],"seq_region_name":"7","id":"rs1798072824","clinical_significance":[]},{"end":140571030,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140571030,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1261080745","seq_region_name":"7"},{"alleles":["T","C"],"end":140571032,"strand":1,"feature_type":"variation","start":140571032,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1222700058","clinical_significance":[]},{"end":140571034,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140571034,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798073319","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140571043,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571043,"clinical_significance":[],"seq_region_name":"7","id":"rs1798073490"},{"source":"dbSNP","start":140571046,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140571046,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1318808646"},{"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140571053,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571053,"source":"dbSNP","seq_region_name":"7","id":"rs1272155366","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571055,"source":"dbSNP","strand":1,"feature_type":"variation","end":140571055,"alleles":["A","T"],"seq_region_name":"7","id":"rs1225245761","clinical_significance":[]},{"end":140571058,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140571058,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585660219","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571062,"feature_type":"variation","strand":1,"end":140571062,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs769786241"},{"feature_type":"variation","strand":1,"end":140571064,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571064,"clinical_significance":[],"seq_region_name":"7","id":"rs1335432517"},{"end":140571067,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140571067,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1798074601","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798074767","source":"dbSNP","start":140571069,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140571069,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571070,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140571070,"clinical_significance":[],"seq_region_name":"7","id":"rs1798074930"},{"seq_region_name":"7","id":"rs910156127","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571085,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140571085},{"seq_region_name":"7","id":"rs538329361","clinical_significance":[],"strand":1,"feature_type":"variation","end":140571086,"alleles":["T","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571086,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1191268600","end":140571091,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140571091,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["TTTT","TT"],"end":140571095,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571092,"source":"dbSNP","seq_region_name":"7","id":"rs1466492350","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140571094,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571094,"clinical_significance":[],"seq_region_name":"7","id":"rs1798075844"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571103,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140571103,"seq_region_name":"7","id":"rs1036730701","clinical_significance":[]},{"clinical_significance":[],"id":"rs2130605006","seq_region_name":"7","alleles":["C","G"],"end":140571108,"feature_type":"variation","strand":1,"source":"dbSNP","start":140571108,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1394095765","seq_region_name":"7","feature_type":"variation","strand":1,"end":140571110,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571110},{"alleles":["C","A"],"end":140571115,"strand":1,"feature_type":"variation","start":140571115,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs539331404","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1160260917","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571122,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140571122},{"seq_region_name":"7","id":"rs918248624","clinical_significance":[],"alleles":["G","A","C"],"end":140571126,"strand":1,"feature_type":"variation","start":140571126,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140571128,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571128,"clinical_significance":[],"seq_region_name":"7","id":"rs518206"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571128,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","-"],"end":140571128,"seq_region_name":"7","id":"rs1798077260","clinical_significance":[]},{"id":"rs1050807307","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140571129,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571129,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1188142766","clinical_significance":[],"start":140571129,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140571130,"alleles":["GG","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1585660375","clinical_significance":[],"end":140571137,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140571137,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571141,"feature_type":"variation","strand":1,"end":140571141,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs575786355"},{"clinical_significance":[],"id":"rs1798078272","seq_region_name":"7","end":140571141,"alleles":["-","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140571142,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798078419","feature_type":"variation","strand":1,"end":140571142,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571142},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140571144,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571144,"source":"dbSNP","seq_region_name":"7","id":"rs889491384","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140571145,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571145,"source":"dbSNP","id":"rs1798078744","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs182815856","seq_region_name":"7","end":140571150,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140571150,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140571152,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140571152,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1798079058","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571158,"feature_type":"variation","strand":1,"end":140571158,"alleles":["T","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1798079229"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1458047113","source":"dbSNP","start":140571160,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140571160,"alleles":["T","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1798079529","clinical_significance":[],"alleles":["TAT","T"],"end":140571162,"strand":1,"feature_type":"variation","start":140571160,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["TATCTAT","TAT"],"end":140571170,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571164,"clinical_significance":[],"id":"rs1275371561","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571166,"feature_type":"variation","strand":1,"end":140571166,"alleles":["T","C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1194350260"},{"id":"rs1798080023","seq_region_name":"7","clinical_significance":[],"end":140571175,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140571175,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140571177,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571177,"source":"dbSNP","seq_region_name":"7","id":"rs1338799337","clinical_significance":[]},{"clinical_significance":[],"id":"rs543519729","seq_region_name":"7","feature_type":"variation","strand":1,"end":140571182,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571182},{"seq_region_name":"7","id":"rs1284895686","clinical_significance":[],"start":140571183,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140571186,"alleles":["AGAG","AG"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140571187,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571187,"clinical_significance":[],"seq_region_name":"7","id":"rs1798080572"},{"seq_region_name":"7","id":"rs1798080735","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571191,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140571191},{"start":140571192,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140571192,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1443183579","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571194,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140571194,"seq_region_name":"7","id":"rs1798081063","clinical_significance":[]},{"end":140571198,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140571198,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798081217"},{"start":140571200,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140571200,"alleles":["C","A"],"strand":1,"feature_type":"variation","id":"rs1248301420","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1381163179","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571203,"source":"dbSNP","strand":1,"feature_type":"variation","end":140571203,"alleles":["G","A"]},{"end":140571206,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140571206,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798081691","clinical_significance":[]},{"alleles":["GG","G"],"end":140571208,"feature_type":"variation","strand":1,"source":"dbSNP","start":140571207,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1314983881"},{"end":140571212,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140571212,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1301430119"},{"alleles":["G","A"],"end":140571218,"feature_type":"variation","strand":1,"source":"dbSNP","start":140571218,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs953075386"},{"clinical_significance":[],"seq_region_name":"7","id":"rs555872252","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140571219,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571219},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140571220,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571220,"source":"dbSNP","id":"rs144545807","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571222,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140571222,"seq_region_name":"7","id":"rs1798082709","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140571223,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571223,"clinical_significance":[],"seq_region_name":"7","id":"rs2130605305"},{"clinical_significance":[],"seq_region_name":"7","id":"rs903796795","alleles":["T","A"],"end":140571224,"feature_type":"variation","strand":1,"source":"dbSNP","start":140571224,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798083019","end":140571227,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140571227,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs561513253","source":"dbSNP","start":140571232,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140571232,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1395110261","clinical_significance":[],"start":140571232,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["CAC","C"],"end":140571234,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571234,"source":"dbSNP","strand":1,"feature_type":"variation","end":140571234,"alleles":["C","A"],"id":"rs1563149770","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798083659","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571235,"source":"dbSNP","strand":1,"feature_type":"variation","end":140571238,"alleles":["CACA","CA"]},{"start":140571238,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140571238,"strand":1,"feature_type":"variation","id":"rs1798083833","seq_region_name":"7","clinical_significance":[]},{"end":140571244,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140571244,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs541445833"},{"seq_region_name":"7","id":"rs999830066","clinical_significance":[],"start":140571245,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140571245,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1314910658","feature_type":"variation","strand":1,"end":140571251,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571251},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140571252,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571252,"source":"dbSNP","seq_region_name":"7","id":"rs667863","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1273719597","alleles":["C","T"],"end":140571257,"feature_type":"variation","strand":1,"source":"dbSNP","start":140571257,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140571261,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571261,"source":"dbSNP","seq_region_name":"7","id":"rs1179884539","clinical_significance":[]},{"end":140571269,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140571269,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1437420947","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140571275,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571275,"clinical_significance":[],"id":"rs1798085364","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571278,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140571278,"seq_region_name":"7","id":"rs1585660706","clinical_significance":[]},{"end":140571279,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140571279,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1469818552","clinical_significance":[]},{"source":"dbSNP","start":140571286,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140571286,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1357376870","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1798086063","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140571287,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571287,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798086239","end":140571288,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140571288,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1798086387","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140571293,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571293,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798086552","source":"dbSNP","start":140571297,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140571297,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571300,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140571300,"seq_region_name":"7","id":"rs1291687835","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140571302,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571302,"clinical_significance":[],"seq_region_name":"7","id":"rs1241581054"},{"clinical_significance":[],"seq_region_name":"7","id":"rs544086945","source":"dbSNP","start":140571303,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C","G"],"end":140571303,"feature_type":"variation","strand":1},{"alleles":["T","C"],"end":140571307,"strand":1,"feature_type":"variation","start":140571307,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1585660767","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140571312,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140571312,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1441981445"},{"seq_region_name":"7","id":"rs1334742555","clinical_significance":[],"strand":1,"feature_type":"variation","end":140571318,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571318,"source":"dbSNP"},{"start":140571320,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140571320,"alleles":["A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1303380641","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140571321,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571321,"clinical_significance":[],"id":"rs1585660807","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1396184922","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140571325,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571325},{"clinical_significance":[],"id":"rs949409610","seq_region_name":"7","source":"dbSNP","start":140571326,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140571326,"alleles":["T","A","C"],"feature_type":"variation","strand":1},{"id":"rs1425994943","seq_region_name":"7","clinical_significance":[],"start":140571326,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140571332,"alleles":["TTTTTTT","TTTTTTTT"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1798088508","seq_region_name":"7","feature_type":"variation","strand":1,"end":140571327,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571327},{"source":"dbSNP","start":140571331,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140571331,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798088644"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571333,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140571333,"clinical_significance":[],"seq_region_name":"7","id":"rs1420272645"},{"clinical_significance":[],"id":"rs1585660851","seq_region_name":"7","source":"dbSNP","start":140571340,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C","G"],"end":140571340,"feature_type":"variation","strand":1},{"id":"rs1798089001","seq_region_name":"7","clinical_significance":[],"start":140571342,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140571342,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140571345,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140571345,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798089105"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571349,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140571349,"clinical_significance":[],"seq_region_name":"7","id":"rs956018634"},{"feature_type":"variation","strand":1,"end":140571350,"alleles":["G","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571350,"clinical_significance":[],"id":"rs59489402","seq_region_name":"7"},{"seq_region_name":"7","id":"rs2130605605","clinical_significance":[],"start":140571350,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140571354,"alleles":["GGGGG","GGGG"],"strand":1,"feature_type":"variation"},{"alleles":["G","C"],"end":140571352,"strand":1,"feature_type":"variation","start":140571352,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1469451013","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140571353,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571353,"source":"dbSNP","seq_region_name":"7","id":"rs1024400635","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798089705","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571354,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140571354},{"strand":1,"feature_type":"variation","end":140571357,"alleles":["TTT","TT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571355,"source":"dbSNP","seq_region_name":"7","id":"rs1563149858","clinical_significance":[]},{"clinical_significance":[],"id":"rs931367056","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140571359,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571359},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140571364,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571364,"source":"dbSNP","id":"rs1798090045","seq_region_name":"7","clinical_significance":[]},{"end":140571370,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140571370,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1798090152","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1178609682","clinical_significance":[],"start":140571373,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140571373,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"end":140571374,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140571374,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs970109578"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1417721446","source":"dbSNP","start":140571375,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140571375,"alleles":["T","C"],"feature_type":"variation","strand":1},{"alleles":["G","A"],"end":140571376,"strand":1,"feature_type":"variation","start":140571376,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798090646","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1217956786","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140571381,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571381},{"source":"dbSNP","start":140571382,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140571382,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1158968876"},{"alleles":["T","C"],"end":140571386,"strand":1,"feature_type":"variation","start":140571386,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1395853859","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140571388,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571388,"clinical_significance":[],"seq_region_name":"7","id":"rs1798091065"},{"clinical_significance":[],"id":"rs1798091168","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571390,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140571390},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571395,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140571395,"id":"rs1798091254","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140571397,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571397,"source":"dbSNP","seq_region_name":"7","id":"rs1798091345","clinical_significance":[]},{"seq_region_name":"7","id":"rs187332267","clinical_significance":[],"strand":1,"feature_type":"variation","end":140571398,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571398,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571401,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140571401,"seq_region_name":"7","id":"rs1798091534","clinical_significance":[]},{"seq_region_name":"7","id":"rs1463514040","clinical_significance":[],"end":140571408,"alleles":["CCC","CCCC"],"strand":1,"feature_type":"variation","start":140571406,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140571407,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140571407,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798091754","clinical_significance":[]},{"id":"rs563873900","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571408,"source":"dbSNP","strand":1,"feature_type":"variation","end":140571408,"alleles":["C","T"]},{"source":"dbSNP","start":140571409,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140571409,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs111993108","seq_region_name":"7"},{"end":140571410,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140571410,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798092233","clinical_significance":[]},{"source":"dbSNP","start":140571411,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140571411,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1004449713","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571415,"feature_type":"variation","strand":1,"end":140571415,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1343058332"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140571416,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571416,"clinical_significance":[],"seq_region_name":"7","id":"rs963030321"},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140571423,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571423,"source":"dbSNP","seq_region_name":"7","id":"rs1443114281","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs973386337","source":"dbSNP","start":140571426,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140571426,"feature_type":"variation","strand":1},{"id":"rs1281500345","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140571427,"alleles":["G","C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571427,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1798092984","clinical_significance":[],"alleles":["T","G"],"end":140571429,"strand":1,"feature_type":"variation","start":140571429,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["G","A"],"end":140571430,"strand":1,"feature_type":"variation","start":140571430,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1316138208","clinical_significance":[]},{"id":"rs1371521610","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571430,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GGG","G"],"end":140571432},{"seq_region_name":"7","id":"rs1222991006","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571436,"source":"dbSNP","strand":1,"feature_type":"variation","end":140571436,"alleles":["A","T"]},{"strand":1,"feature_type":"variation","end":140571437,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571437,"source":"dbSNP","seq_region_name":"7","id":"rs1293721130","clinical_significance":[]},{"clinical_significance":[],"id":"rs1399892834","seq_region_name":"7","end":140571438,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140571438,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571439,"feature_type":"variation","strand":1,"alleles":["GG","G"],"end":140571440,"clinical_significance":[],"seq_region_name":"7","id":"rs1798093533"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798093643","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571443,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140571443},{"seq_region_name":"7","id":"rs1798093768","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571447,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140571447},{"id":"rs1798093877","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140571448,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571448,"source":"dbSNP"},{"end":140571450,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140571450,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1429812048"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571451,"feature_type":"variation","strand":1,"end":140571451,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs759292825"},{"seq_region_name":"7","id":"rs55816014","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571452,"source":"dbSNP","strand":1,"feature_type":"variation","end":140571452,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1028629763","source":"dbSNP","start":140571457,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140571457,"alleles":["G","T"],"feature_type":"variation","strand":1},{"alleles":["C","T"],"end":140571459,"strand":1,"feature_type":"variation","start":140571459,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs953127551","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571470,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140571470,"seq_region_name":"7","id":"rs1486890369","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571471,"feature_type":"variation","strand":1,"end":140571471,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1798094593"},{"seq_region_name":"7","id":"rs1240856153","clinical_significance":[],"start":140571472,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140571472,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1798094801","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571475,"source":"dbSNP","strand":1,"feature_type":"variation","end":140571475,"alleles":["C","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1271945196","end":140571476,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140571476,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1563149976","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571487,"source":"dbSNP","strand":1,"feature_type":"variation","end":140571487,"alleles":["A","G"]},{"id":"rs1050695485","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140571488,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571488,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1443329152","seq_region_name":"7","end":140571489,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140571489,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140571498,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571498,"clinical_significance":[],"seq_region_name":"7","id":"rs1000600864"},{"alleles":["C","A","T"],"end":140571506,"strand":1,"feature_type":"variation","start":140571506,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs910983764","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs942429348","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571507,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140571507},{"end":140571508,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140571508,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1206114003"},{"clinical_significance":[],"id":"rs1230806235","seq_region_name":"7","end":140571509,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140571509,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140571513,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571513,"clinical_significance":[],"id":"rs1798095897","seq_region_name":"7"},{"seq_region_name":"7","id":"rs2130606029","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571513,"source":"dbSNP","strand":1,"feature_type":"variation","end":140571513,"alleles":["C","CC"]},{"end":140571514,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140571514,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs917827494","seq_region_name":"7"},{"id":"rs1043588992","seq_region_name":"7","clinical_significance":[],"end":140571515,"alleles":["T","C","G"],"strand":1,"feature_type":"variation","start":140571515,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1480145891","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571517,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140571517},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798096356","feature_type":"variation","strand":1,"end":140571518,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571518},{"end":140571523,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140571523,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798096475","clinical_significance":[]},{"source":"dbSNP","start":140571527,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140571527,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs568192324"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140571528,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571528,"clinical_significance":[],"id":"rs1798096834","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140571529,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571529,"source":"dbSNP","seq_region_name":"7","id":"rs1798097003","clinical_significance":[]},{"end":140571537,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140571537,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs903682748","clinical_significance":[]},{"alleles":["G","A"],"end":140571538,"strand":1,"feature_type":"variation","start":140571538,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1563150014","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798097579","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571539,"source":"dbSNP","strand":1,"feature_type":"variation","end":140571539,"alleles":["C","A"]},{"clinical_significance":[],"id":"rs1798097696","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571541,"feature_type":"variation","strand":1,"end":140571541,"alleles":["A","G"]},{"alleles":["G","C","T"],"end":140571546,"feature_type":"variation","strand":1,"source":"dbSNP","start":140571546,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585661355"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798097944","feature_type":"variation","strand":1,"end":140571547,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571547},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140571551,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571551,"clinical_significance":[],"id":"rs970635784","seq_region_name":"7"},{"alleles":["T","C"],"end":140571555,"strand":1,"feature_type":"variation","start":140571555,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1798098166","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798098270","source":"dbSNP","start":140571556,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140571556,"alleles":["A","G"],"feature_type":"variation","strand":1},{"alleles":["T","A"],"end":140571557,"feature_type":"variation","strand":1,"source":"dbSNP","start":140571557,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs528958268"},{"seq_region_name":"7","id":"rs999484659","clinical_significance":[],"start":140571567,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140571567,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1798098602","clinical_significance":[],"end":140571569,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140571569,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs547403852","feature_type":"variation","strand":1,"end":140571570,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571570},{"start":140571574,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140571574,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798098827","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140571576,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571576,"source":"dbSNP","seq_region_name":"7","id":"rs1052359111","clinical_significance":[]},{"source":"dbSNP","start":140571577,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140571577,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs896365572"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571585,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140571585,"seq_region_name":"7","id":"rs1338396832","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798099288","source":"dbSNP","start":140571587,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140571587,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1798099388","clinical_significance":[],"strand":1,"feature_type":"variation","end":140571592,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571592,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571597,"source":"dbSNP","strand":1,"feature_type":"variation","end":140571597,"alleles":["G","A"],"id":"rs1798099495","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1563150038","clinical_significance":[],"start":140571601,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140571601,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs765733780","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140571612,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571612,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs931420872","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140571615,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571615},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571622,"feature_type":"variation","strand":1,"end":140571651,"alleles":["AACACTCCAACTTTCTAACAGCCAAGTGTC","-"],"clinical_significance":[],"id":"rs1585661460","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585661469","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571625,"feature_type":"variation","strand":1,"end":140571625,"alleles":["A","C"]},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140571628,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571628,"source":"dbSNP","id":"rs1476447117","seq_region_name":"7","clinical_significance":[]},{"end":140571631,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140571631,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1014285262","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1430381437","seq_region_name":"7","feature_type":"variation","strand":1,"end":140571640,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571640},{"strand":1,"feature_type":"variation","end":140571647,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571647,"source":"dbSNP","seq_region_name":"7","id":"rs1798100705","clinical_significance":[]},{"source":"dbSNP","start":140571652,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140571652,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1417511343"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571653,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140571653,"clinical_significance":[],"seq_region_name":"7","id":"rs1798101037"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1163404473","alleles":["T","C"],"end":140571654,"feature_type":"variation","strand":1,"source":"dbSNP","start":140571654,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571658,"feature_type":"variation","strand":1,"end":140571658,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1445716774"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1245545836","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571659,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140571659},{"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140571666,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571666,"clinical_significance":[],"seq_region_name":"7","id":"rs1798101561"},{"seq_region_name":"7","id":"rs562477456","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571671,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140571671},{"source":"dbSNP","start":140571683,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["-","TATATACATTTTGTATATACATC"],"end":140571682,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798101787"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571683,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140571683,"seq_region_name":"7","id":"rs1798101884","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798101984","source":"dbSNP","start":140571684,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140571684,"alleles":["T","C"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140571686,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140571686,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1410589901"},{"clinical_significance":[],"seq_region_name":"7","id":"rs908748620","source":"dbSNP","start":140571688,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140571688,"alleles":["T","C"],"feature_type":"variation","strand":1},{"alleles":["C","T"],"end":140571690,"strand":1,"feature_type":"variation","start":140571690,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs940190658","clinical_significance":[]},{"seq_region_name":"7","id":"rs1308713773","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140571691,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571691,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs905978617","source":"dbSNP","start":140571692,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140571692,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs192112795","source":"dbSNP","start":140571694,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140571694,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs565505262","source":"dbSNP","start":140571695,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140571695,"feature_type":"variation","strand":1},{"id":"rs139638321","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140571697,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571697,"source":"dbSNP"},{"seq_region_name":"7","id":"rs963210844","clinical_significance":[],"start":140571700,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140571700,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"id":"rs1450172082","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571704,"source":"dbSNP","strand":1,"feature_type":"variation","end":140571704,"alleles":["C","T"]},{"feature_type":"variation","strand":1,"end":140571709,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571709,"clinical_significance":[],"seq_region_name":"7","id":"rs1798103157"},{"seq_region_name":"7","id":"rs1585661639","clinical_significance":[],"end":140571710,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140571710,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140571713,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571713,"clinical_significance":[],"id":"rs1381855991","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1298932414","clinical_significance":[],"start":140571716,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140571721,"alleles":["AAAAAA","AA"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798103551","source":"dbSNP","start":140571721,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140571721,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1798103660","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571722,"feature_type":"variation","strand":1,"end":140571722,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1463768617","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571725,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140571725},{"clinical_significance":[],"id":"rs1352948448","seq_region_name":"7","end":140571728,"alleles":["A","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140571728,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","G","T"],"end":140571732,"strand":1,"feature_type":"variation","start":140571732,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585661693","clinical_significance":[]},{"id":"rs532910174","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140571738,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571738,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130606504","feature_type":"variation","strand":1,"end":140571741,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571741},{"clinical_significance":[],"seq_region_name":"7","id":"rs972834035","feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140571743,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571743},{"clinical_significance":[],"seq_region_name":"7","id":"rs1169779281","end":140571763,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140571763,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140571768,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140571768,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1798104511","seq_region_name":"7"},{"seq_region_name":"7","id":"rs79496716","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571770,"source":"dbSNP","strand":1,"feature_type":"variation","end":140571770,"alleles":["G","A"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571771,"source":"dbSNP","strand":1,"feature_type":"variation","end":140571773,"alleles":["AAA","AA"],"seq_region_name":"7","id":"rs1387567707","clinical_significance":[]},{"seq_region_name":"7","id":"rs1182352303","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571773,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140571773},{"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140571790,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571790,"source":"dbSNP","seq_region_name":"7","id":"rs775075111","clinical_significance":[]},{"end":140571791,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140571791,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs569606975"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571803,"source":"dbSNP","strand":1,"feature_type":"variation","end":140571803,"alleles":["T","C"],"seq_region_name":"7","id":"rs1412787326","clinical_significance":[]},{"alleles":["A","AA"],"end":140571811,"strand":1,"feature_type":"variation","start":140571811,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs140641336","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1249288248","end":140571812,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140571812,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130606599","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571813,"feature_type":"variation","strand":1,"end":140571813,"alleles":["C","G"]},{"alleles":["TGAGAT","T"],"end":140571819,"strand":1,"feature_type":"variation","start":140571814,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1340057774","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571818,"feature_type":"variation","strand":1,"end":140571818,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130606619"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130606628","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571830,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140571830},{"source":"dbSNP","start":140571831,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140571831,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs2130606637","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571836,"feature_type":"variation","strand":1,"end":140571836,"alleles":["C","T"],"clinical_significance":[],"id":"rs888772597","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798105754","end":140571837,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140571837,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140571848,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140571848,"strand":1,"feature_type":"variation","id":"rs761018518","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1798105948","seq_region_name":"7","source":"dbSNP","start":140571849,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140571849,"alleles":["A","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798106063","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571855,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140571855},{"clinical_significance":[],"seq_region_name":"7","id":"rs1000653375","feature_type":"variation","strand":1,"end":140571856,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571856},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571857,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140571857,"seq_region_name":"7","id":"rs1032093684","clinical_significance":[]},{"seq_region_name":"7","id":"rs1381744980","clinical_significance":[],"end":140571861,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140571861,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140571867,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140571867,"strand":1,"feature_type":"variation","id":"rs2130606706","seq_region_name":"7","clinical_significance":[]},{"id":"rs910869032","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140571870,"strand":1,"feature_type":"variation","start":140571870,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798106618","alleles":["C","T"],"end":140571877,"feature_type":"variation","strand":1,"source":"dbSNP","start":140571877,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1307385431","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571879,"source":"dbSNP","strand":1,"feature_type":"variation","end":140571879,"alleles":["T","A"]},{"clinical_significance":[],"id":"rs1798106822","seq_region_name":"7","feature_type":"variation","strand":1,"end":140571880,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571880},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571882,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140571882,"clinical_significance":[],"seq_region_name":"7","id":"rs956401541"},{"id":"rs114617550","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140571886,"strand":1,"feature_type":"variation","start":140571886,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571897,"source":"dbSNP","strand":1,"feature_type":"variation","end":140571897,"alleles":["C","G"],"seq_region_name":"7","id":"rs1211189310","clinical_significance":[]},{"source":"dbSNP","start":140571900,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140571900,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1258611179"},{"start":140571902,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140571902,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798107267","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798107378","clinical_significance":[],"strand":1,"feature_type":"variation","end":140571904,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571904,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1798107474","clinical_significance":[],"end":140571906,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140571906,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798107587","source":"dbSNP","start":140571907,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140571907,"alleles":["T","C","G"],"feature_type":"variation","strand":1},{"alleles":["C","T"],"end":140571909,"feature_type":"variation","strand":1,"source":"dbSNP","start":140571909,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs754192045","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1798107815","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571911,"source":"dbSNP","strand":1,"feature_type":"variation","end":140571911,"alleles":["G","A"]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140571917,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571917,"clinical_significance":[],"id":"rs2130606803","seq_region_name":"7"},{"alleles":["C","T"],"end":140571927,"feature_type":"variation","strand":1,"source":"dbSNP","start":140571927,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585662039"},{"feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140571928,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571928,"clinical_significance":[],"seq_region_name":"7","id":"rs1798108001"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140571929,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571929,"source":"dbSNP","seq_region_name":"7","id":"rs56711326","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs980693869","end":140571930,"alleles":["T","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140571930,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140571934,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571934,"source":"dbSNP","seq_region_name":"7","id":"rs2130606837","clinical_significance":[]},{"id":"rs1424637766","seq_region_name":"7","clinical_significance":[],"end":140571942,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140571942,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140571947,"alleles":["AAA","AAAA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571945,"clinical_significance":[],"seq_region_name":"7","id":"rs1186319343"},{"feature_type":"variation","strand":1,"end":140571949,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571949,"clinical_significance":[],"seq_region_name":"7","id":"rs144574647"},{"end":140571951,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140571951,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1476049312"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571952,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140571952,"clinical_significance":[],"id":"rs1052246494","seq_region_name":"7"},{"alleles":["T","C"],"end":140571955,"strand":1,"feature_type":"variation","start":140571955,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1169700057","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798109025","source":"dbSNP","start":140571956,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["CCC","CC"],"end":140571958,"feature_type":"variation","strand":1},{"alleles":["C","T"],"end":140571957,"strand":1,"feature_type":"variation","start":140571957,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1247904866","seq_region_name":"7","clinical_significance":[]},{"end":140571958,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140571958,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs896419648"},{"clinical_significance":[],"seq_region_name":"7","id":"rs534778074","source":"dbSNP","start":140571963,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140571963,"alleles":["T","C"],"feature_type":"variation","strand":1},{"end":140571966,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140571966,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798109466","clinical_significance":[]},{"end":140571967,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140571967,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798109577"},{"clinical_significance":[],"id":"rs1270476925","seq_region_name":"7","alleles":["T","C"],"end":140571968,"feature_type":"variation","strand":1,"source":"dbSNP","start":140571968,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571970,"source":"dbSNP","strand":1,"feature_type":"variation","end":140571970,"alleles":["C","-"],"seq_region_name":"7","id":"rs1644116375","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571974,"feature_type":"variation","strand":1,"end":140571974,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1174502113"},{"seq_region_name":"7","id":"rs1585662143","clinical_significance":[],"start":140571977,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140571977,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798109992","end":140571981,"alleles":["AT","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140571980,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571981,"feature_type":"variation","strand":1,"end":140571981,"alleles":["T","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1798110088"},{"clinical_significance":[],"seq_region_name":"7","id":"rs58273598","end":140572003,"alleles":["TCTCTCTCTCTCTCTCTCTCTCT","TCTCTCTCTCT","TCTCTCTCTCTCT","TCTCTCTCTCTCTCT","TCTCTCTCTCTCTCTCT","TCTCTCTCTCTCTCTCTCT","TCTCTCTCTCTCTCTCTCTCT","TCTCTCTCTCTCTCTCTCTCTCTCT","TCTCTCTCTCTCTCTCTCTCTCTCTCT","TCTCTCTCTCTCTCTCTCTCTCTCTCTCT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140571981,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1585662203","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140571982,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571982},{"strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140571989,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571989,"source":"dbSNP","seq_region_name":"7","id":"rs1798110770","clinical_significance":[]},{"id":"rs1798110902","seq_region_name":"7","clinical_significance":[],"start":140571989,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140572011,"alleles":["TCTCTCTCTCTCTCTGTCTCTCT","TCTCTCT"],"strand":1,"feature_type":"variation"},{"end":140571990,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140571990,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798111016","clinical_significance":[]},{"id":"rs1585662211","seq_region_name":"7","clinical_significance":[],"alleles":["C","G","T"],"end":140571992,"strand":1,"feature_type":"variation","start":140571992,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798111236","source":"dbSNP","start":140571992,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140571992,"alleles":["C","-"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571992,"source":"dbSNP","strand":1,"feature_type":"variation","end":140571994,"alleles":["CTC","T"],"seq_region_name":"7","id":"rs796496798","clinical_significance":[]},{"seq_region_name":"7","id":"rs1404441782","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140571993,"source":"dbSNP","strand":1,"feature_type":"variation","end":140572011,"alleles":["TCTCTCTCTCTGTCTCTCT","TCTCTCT"]},{"seq_region_name":"7","id":"rs1386223333","clinical_significance":[],"start":140571994,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140571994,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1798111654","clinical_significance":[],"end":140571994,"alleles":["C","-"],"strand":1,"feature_type":"variation","start":140571994,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs758670040","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140571996,"feature_type":"variation","strand":1,"end":140571996,"alleles":["C","G","T"]},{"start":140572000,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140572000,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798111884","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140572002,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572002,"source":"dbSNP","seq_region_name":"7","id":"rs553357617","clinical_significance":[]},{"id":"rs1798112073","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572003,"source":"dbSNP","strand":1,"feature_type":"variation","end":140572005,"alleles":["TGT","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572004,"source":"dbSNP","strand":1,"feature_type":"variation","end":140572004,"alleles":["G","C"],"seq_region_name":"7","id":"rs184656069","clinical_significance":[]},{"end":140572005,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140572005,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798112277","clinical_significance":[]},{"id":"rs1452081878","seq_region_name":"7","clinical_significance":[],"start":140572005,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140572011,"alleles":["TCTCTCT","TCTCT"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1798112496","clinical_significance":[],"alleles":["C","T"],"end":140572006,"strand":1,"feature_type":"variation","start":140572006,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798112595","source":"dbSNP","start":140572007,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140572007,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140572008,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572008,"clinical_significance":[],"seq_region_name":"7","id":"rs1798112684"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798112798","feature_type":"variation","strand":1,"end":140572014,"alleles":["TCTTTT","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572009},{"clinical_significance":[],"seq_region_name":"7","id":"rs1363630201","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140572019,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572019},{"seq_region_name":"7","id":"rs1798113003","clinical_significance":[],"start":140572020,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140572020,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572022,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140572022,"clinical_significance":[],"seq_region_name":"7","id":"rs372081317"},{"id":"rs1798113799","seq_region_name":"7","clinical_significance":[],"start":140572026,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140572026,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140572030,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572030,"clinical_significance":[],"seq_region_name":"7","id":"rs984209731"},{"start":140572034,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140572034,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs560255958","clinical_significance":[]},{"source":"dbSNP","start":140572035,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140572035,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs940092123"},{"start":140572037,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140572037,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1196564722","clinical_significance":[]},{"source":"dbSNP","start":140572038,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140572038,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798114702"},{"source":"dbSNP","start":140572055,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140572055,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs189370619"},{"start":140572056,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140572056,"strand":1,"feature_type":"variation","id":"rs1585662344","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs922777364","clinical_significance":[],"strand":1,"feature_type":"variation","end":140572058,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572058,"source":"dbSNP"},{"start":140572063,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140572063,"alleles":["G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs905849229","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572064,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140572064,"id":"rs1206896434","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572065,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140572065,"seq_region_name":"7","id":"rs1267851414","clinical_significance":[]},{"id":"rs1798115626","seq_region_name":"7","clinical_significance":[],"start":140572072,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140572072,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140572073,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572073,"source":"dbSNP","seq_region_name":"7","id":"rs1798115720","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798115822","clinical_significance":[],"alleles":["C","A"],"end":140572075,"strand":1,"feature_type":"variation","start":140572075,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572079,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140572079,"clinical_significance":[],"seq_region_name":"7","id":"rs1484752928"},{"start":140572080,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140572080,"alleles":["T","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1267316714","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798116131","clinical_significance":[],"strand":1,"feature_type":"variation","end":140572081,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572081,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1001508085","end":140572082,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140572082,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140572084,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140572084,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1325875560","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572085,"source":"dbSNP","strand":1,"feature_type":"variation","end":140572085,"alleles":["C","G"],"id":"rs1798116432","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572087,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140572087,"clinical_significance":[],"seq_region_name":"7","id":"rs1281616407"},{"alleles":["A","G"],"end":140572090,"feature_type":"variation","strand":1,"source":"dbSNP","start":140572090,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1017434952"},{"source":"dbSNP","start":140572094,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140572094,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1049998848"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1298337038","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572095,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140572095},{"feature_type":"variation","strand":1,"end":140572096,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572096,"clinical_significance":[],"seq_region_name":"7","id":"rs527356727"},{"seq_region_name":"7","id":"rs898554502","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140572107,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572107,"source":"dbSNP"},{"start":140572110,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TCTCTCTC","TCTC"],"end":140572117,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1363873076","clinical_significance":[]},{"start":140572119,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140572119,"strand":1,"feature_type":"variation","id":"rs1798117337","seq_region_name":"7","clinical_significance":[]},{"start":140572125,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140572125,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798117428","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572128,"feature_type":"variation","strand":1,"end":140572128,"alleles":["C","G"],"clinical_significance":[],"id":"rs1798117520","seq_region_name":"7"},{"source":"dbSNP","start":140572129,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","-"],"end":140572129,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1337761448"},{"alleles":["A","G"],"end":140572131,"feature_type":"variation","strand":1,"source":"dbSNP","start":140572131,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1798117713","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1798117817","clinical_significance":[],"start":140572135,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140572135,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140572141,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572141,"source":"dbSNP","seq_region_name":"7","id":"rs545722124","clinical_significance":[]},{"source":"dbSNP","start":140572143,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140572143,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1281999721"},{"seq_region_name":"7","id":"rs779940402","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572146,"source":"dbSNP","strand":1,"feature_type":"variation","end":140572146,"alleles":["C","A"]},{"seq_region_name":"7","id":"rs1209135890","clinical_significance":[],"start":140572148,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140572148,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1173884867","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572150,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140572150},{"end":140572155,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140572155,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798118516"},{"source":"dbSNP","start":140572156,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140572156,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1278418168"},{"seq_region_name":"7","id":"rs1798118733","clinical_significance":[],"strand":1,"feature_type":"variation","end":140572157,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572157,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1477406349","clinical_significance":[],"end":140572159,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140572159,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140572176,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572176,"source":"dbSNP","id":"rs888821644","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","C"],"end":140572177,"strand":1,"feature_type":"variation","start":140572177,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585662583","clinical_significance":[]},{"alleles":["A","G","T"],"end":140572179,"strand":1,"feature_type":"variation","start":140572179,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1426613711","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140572180,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572180,"source":"dbSNP","seq_region_name":"7","id":"rs1798119231","clinical_significance":[]},{"seq_region_name":"7","id":"rs1195993087","clinical_significance":[],"end":140572187,"alleles":["TTTTTTTT","TTTTTTT","TTTTTTTTT"],"strand":1,"feature_type":"variation","start":140572180,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1798119482","clinical_significance":[],"strand":1,"feature_type":"variation","end":140572182,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572182,"source":"dbSNP"},{"source":"dbSNP","start":140572183,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140572183,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798119577"},{"strand":1,"feature_type":"variation","end":140572186,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572186,"source":"dbSNP","seq_region_name":"7","id":"rs2130607509","clinical_significance":[]},{"clinical_significance":[],"id":"rs1798119670","seq_region_name":"7","feature_type":"variation","strand":1,"end":140572188,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572188},{"id":"rs193045692","seq_region_name":"7","clinical_significance":[],"start":140572193,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140572193,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1203985929","clinical_significance":[],"end":140572194,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140572194,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140572196,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140572199,"alleles":["GGGG","GGG"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798119975","clinical_significance":[]},{"alleles":["G","A"],"end":140572197,"strand":1,"feature_type":"variation","start":140572197,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1025755494","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140572199,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572199,"clinical_significance":[],"seq_region_name":"7","id":"rs185744128"},{"alleles":["C","T"],"end":140572203,"strand":1,"feature_type":"variation","start":140572203,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1200137936","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572205,"source":"dbSNP","strand":1,"feature_type":"variation","end":140572205,"alleles":["C","A","T"],"seq_region_name":"7","id":"rs892236250","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798120587","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572208,"feature_type":"variation","strand":1,"end":140572208,"alleles":["T","A"]},{"id":"rs1798120697","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140572210,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572210,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572212,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140572212,"seq_region_name":"7","id":"rs1253106160","clinical_significance":[]},{"seq_region_name":"7","id":"rs987009227","clinical_significance":[],"alleles":["C","T"],"end":140572214,"strand":1,"feature_type":"variation","start":140572214,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798121028","alleles":["C","T"],"end":140572215,"feature_type":"variation","strand":1,"source":"dbSNP","start":140572215,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1194413198","source":"dbSNP","start":140572217,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140572217,"alleles":["G","C"],"feature_type":"variation","strand":1},{"id":"rs1316370936","seq_region_name":"7","clinical_significance":[],"start":140572226,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140572226,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798121362","alleles":["G","C"],"end":140572227,"feature_type":"variation","strand":1,"source":"dbSNP","start":140572227,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798121476","feature_type":"variation","strand":1,"end":140572231,"alleles":["T","C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572231},{"alleles":["C","G","T"],"end":140572232,"strand":1,"feature_type":"variation","start":140572232,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs543231956","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140572234,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572234,"clinical_significance":[],"seq_region_name":"7","id":"rs964058144"},{"id":"rs1798121875","seq_region_name":"7","clinical_significance":[],"end":140572235,"alleles":["-","AC"],"strand":1,"feature_type":"variation","start":140572236,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798121986","source":"dbSNP","start":140572236,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140572236,"feature_type":"variation","strand":1},{"end":140572242,"alleles":["TAAA","-"],"strand":1,"feature_type":"variation","start":140572239,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798122093","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798122211","clinical_significance":[],"end":140572241,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140572241,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1334250701","feature_type":"variation","strand":1,"end":140572242,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572242},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798122416","source":"dbSNP","start":140572243,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140572243,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs561307771","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572250,"feature_type":"variation","strand":1,"end":140572250,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1396792410","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572252,"source":"dbSNP","strand":1,"feature_type":"variation","end":140572252,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1169100985","clinical_significance":[],"start":140572259,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140572259,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572260,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140572260,"clinical_significance":[],"seq_region_name":"7","id":"rs1798122884"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572262,"feature_type":"variation","strand":1,"end":140572262,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1798122999"},{"seq_region_name":"7","id":"rs1460026348","clinical_significance":[],"start":140572265,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140572265,"strand":1,"feature_type":"variation"},{"alleles":["A","G"],"end":140572268,"strand":1,"feature_type":"variation","start":140572268,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1585662765","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798123281","clinical_significance":[],"end":140572270,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140572270,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140572273,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140572273,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1798123387","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1389414347","clinical_significance":[],"strand":1,"feature_type":"variation","end":140572276,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572276,"source":"dbSNP"},{"seq_region_name":"7","id":"rs368826761","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140572278,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572278,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798123679","end":140572281,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140572281,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140572282,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140572282,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1184191265","clinical_significance":[]},{"seq_region_name":"7","id":"rs1002565806","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572286,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140572286},{"clinical_significance":[],"id":"rs548951592","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572287,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140572287},{"seq_region_name":"7","id":"rs1241099687","clinical_significance":[],"start":140572289,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140572289,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1186610905","end":140572294,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140572294,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140572295,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140572295,"strand":1,"feature_type":"variation","id":"rs189008749","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs547149382","feature_type":"variation","strand":1,"end":140572300,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572300},{"seq_region_name":"7","id":"rs1798124380","clinical_significance":[],"start":140572308,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140572308,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"start":140572310,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140572310,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1252937328","clinical_significance":[]},{"start":140572311,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140572311,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798124614","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572313,"source":"dbSNP","strand":1,"feature_type":"variation","end":140572313,"alleles":["G","A"],"seq_region_name":"7","id":"rs2130607865","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572326,"feature_type":"variation","strand":1,"end":140572326,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1385434300"},{"seq_region_name":"7","id":"rs952591466","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572330,"source":"dbSNP","strand":1,"feature_type":"variation","end":140572330,"alleles":["A","G"]},{"source":"dbSNP","start":140572331,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140572331,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1341620329"},{"clinical_significance":[],"seq_region_name":"7","id":"rs567444557","source":"dbSNP","start":140572336,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140572336,"feature_type":"variation","strand":1},{"end":140572341,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140572341,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs984098695","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1402337132","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572342,"source":"dbSNP","strand":1,"feature_type":"variation","end":140572342,"alleles":["G","A"]},{"strand":1,"feature_type":"variation","end":140572344,"alleles":["G","C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572344,"source":"dbSNP","id":"rs1798125389","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130607943","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140572349,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572349,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572350,"source":"dbSNP","strand":1,"feature_type":"variation","end":140572350,"alleles":["C","T"],"seq_region_name":"7","id":"rs1357713289","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572351,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140572351,"id":"rs1798125756","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1283922242","clinical_significance":[],"start":140572352,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140572352,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572353,"source":"dbSNP","strand":1,"feature_type":"variation","end":140572353,"alleles":["T","A"],"id":"rs180917725","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572361,"feature_type":"variation","strand":1,"alleles":["ACAGACAG","ACAG"],"end":140572368,"clinical_significance":[],"seq_region_name":"7","id":"rs1335911144"},{"id":"rs1316141611","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140572364,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572364,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572367,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140572367,"seq_region_name":"7","id":"rs1798126264","clinical_significance":[]},{"start":140572376,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140572376,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs988004473","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572377,"feature_type":"variation","strand":1,"end":140572377,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1798126518"},{"feature_type":"variation","strand":1,"end":140572379,"alleles":["C","A","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572379,"clinical_significance":[],"id":"rs1369468643","seq_region_name":"7"},{"source":"dbSNP","start":140572380,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140572380,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs976848926","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs922794037","end":140572382,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140572382,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140572384,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572384,"clinical_significance":[],"seq_region_name":"7","id":"rs932830992"},{"id":"rs1798127034","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572387,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140572387},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798127140","feature_type":"variation","strand":1,"end":140572390,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572390},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140572395,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572395,"clinical_significance":[],"id":"rs917740299","seq_region_name":"7"},{"source":"dbSNP","start":140572396,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140572396,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798127336"},{"end":140572397,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140572397,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1563150465","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140572398,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572398,"source":"dbSNP","seq_region_name":"7","id":"rs1470398775","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798127653","source":"dbSNP","start":140572399,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140572399,"alleles":["T","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1798127767","clinical_significance":[],"strand":1,"feature_type":"variation","end":140572401,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572401,"source":"dbSNP"},{"end":140572404,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140572404,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1234805511","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1180012082","feature_type":"variation","strand":1,"end":140572411,"alleles":["A","C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572411},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798128019","end":140572412,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140572412,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798128194","alleles":["G","A"],"end":140572415,"feature_type":"variation","strand":1,"source":"dbSNP","start":140572415,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140572425,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572425,"source":"dbSNP","seq_region_name":"7","id":"rs1305037230","clinical_significance":[]},{"clinical_significance":[],"id":"rs1798129320","seq_region_name":"7","end":140572436,"alleles":["CCCTAAAGCCC","CCC"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140572426,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1368304057","source":"dbSNP","start":140572430,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140572432,"alleles":["AAA","AA"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585663136","alleles":["A","G"],"end":140572431,"feature_type":"variation","strand":1,"source":"dbSNP","start":140572431,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1798129937","clinical_significance":[],"start":140572434,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140572434,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"end":140572435,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140572435,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1232102180","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140572436,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140572436,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1489990932","seq_region_name":"7"},{"id":"rs1289797273","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140572441,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572441,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572446,"source":"dbSNP","strand":1,"feature_type":"variation","end":140572446,"alleles":["C","A"],"seq_region_name":"7","id":"rs2130608210","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798130414","feature_type":"variation","strand":1,"end":140572448,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572448},{"seq_region_name":"7","id":"rs985585015","clinical_significance":[],"alleles":["T","G"],"end":140572455,"strand":1,"feature_type":"variation","start":140572455,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1353359263","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572460,"source":"dbSNP","strand":1,"feature_type":"variation","end":140572460,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs752050283","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572461,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140572461},{"seq_region_name":"7","id":"rs1798131129","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572462,"source":"dbSNP","strand":1,"feature_type":"variation","end":140572462,"alleles":["C","A"]},{"id":"rs1226229614","seq_region_name":"7","clinical_significance":[],"start":140572471,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140572471,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1349522927","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140572475,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572475},{"id":"rs1798131471","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572476,"source":"dbSNP","strand":1,"feature_type":"variation","end":140572476,"alleles":["T","A"]},{"end":140572478,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140572478,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1303193056"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572482,"feature_type":"variation","strand":1,"end":140572482,"alleles":["G","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1406253464"},{"source":"dbSNP","start":140572483,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140572483,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1274589094"},{"clinical_significance":[],"seq_region_name":"7","id":"rs34444128","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572485,"feature_type":"variation","strand":1,"end":140572487,"alleles":["GGG","GG"]},{"start":140572486,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140572486,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs201719470","clinical_significance":[]},{"id":"rs113906865","seq_region_name":"7","clinical_significance":[],"start":140572487,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140572487,"strand":1,"feature_type":"variation"},{"start":140572490,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140572490,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1207351634","clinical_significance":[]},{"seq_region_name":"7","id":"rs112473320","clinical_significance":[],"start":140572491,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140572491,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1409941737","clinical_significance":[],"end":140572495,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140572495,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs905068486","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572498,"source":"dbSNP","strand":1,"feature_type":"variation","end":140572498,"alleles":["C","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572499,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140572499,"seq_region_name":"7","id":"rs1585663312","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798132934","clinical_significance":[],"start":140572500,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A","C","G"],"end":140572500,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1270169952","source":"dbSNP","start":140572503,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140572503,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572505,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140572505,"clinical_significance":[],"seq_region_name":"7","id":"rs937354618"},{"end":140572510,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140572510,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1201599693","seq_region_name":"7"},{"start":140572512,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140572512,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs569643983","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572514,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140572514,"clinical_significance":[],"seq_region_name":"7","id":"rs1798133606"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572517,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140572517,"clinical_significance":[],"seq_region_name":"7","id":"rs536934640"},{"end":140572519,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140572519,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1449064486","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798133994","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572523,"feature_type":"variation","strand":1,"end":140572523,"alleles":["G","A"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572533,"source":"dbSNP","strand":1,"feature_type":"variation","end":140572533,"alleles":["C","T"],"seq_region_name":"7","id":"rs1585663378","clinical_significance":[]},{"source":"dbSNP","start":140572537,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140572537,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1417792914","seq_region_name":"7"},{"alleles":["G","A"],"end":140572538,"strand":1,"feature_type":"variation","start":140572538,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs549178412","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140572540,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140572540,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585663399"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572541,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140572541,"clinical_significance":[],"seq_region_name":"7","id":"rs1585663405"},{"source":"dbSNP","start":140572542,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140572542,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs567323461"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140572544,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572544,"clinical_significance":[],"seq_region_name":"7","id":"rs1798134830"},{"clinical_significance":[],"seq_region_name":"7","id":"rs906398611","feature_type":"variation","strand":1,"end":140572547,"alleles":["CGCG","CG"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572544},{"end":140572545,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140572545,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs535117320","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140572546,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572546,"clinical_significance":[],"id":"rs553148454","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1364962390","clinical_significance":[],"alleles":["G","A"],"end":140572547,"strand":1,"feature_type":"variation","start":140572547,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1585663452","clinical_significance":[],"alleles":["T","G"],"end":140572549,"strand":1,"feature_type":"variation","start":140572549,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140572552,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140572552,"alleles":["G","C"],"strand":1,"feature_type":"variation","id":"rs1798135528","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs578135608","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572558,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","G","T"],"end":140572558},{"end":140572559,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140572559,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs539080897","seq_region_name":"7","clinical_significance":[]},{"end":140572562,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140572562,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1456510374","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1156660239","clinical_significance":[],"alleles":["C","T"],"end":140572568,"strand":1,"feature_type":"variation","start":140572568,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1798136264","seq_region_name":"7","clinical_significance":[],"end":140572570,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140572570,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1018944772","clinical_significance":[],"start":140572571,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140572571,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572572,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140572572,"seq_region_name":"7","id":"rs2130608550","clinical_significance":[]},{"source":"dbSNP","start":140572573,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140572573,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1015576711"},{"id":"rs1798136625","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140572576,"strand":1,"feature_type":"variation","start":140572576,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1187587411","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572578,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140572578},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572579,"feature_type":"variation","strand":1,"end":140572579,"alleles":["G","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1798136855"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572586,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140572586,"clinical_significance":[],"seq_region_name":"7","id":"rs1476654090"},{"seq_region_name":"7","id":"rs1798137084","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572588,"source":"dbSNP","strand":1,"feature_type":"variation","end":140572588,"alleles":["C","T"]},{"end":140572589,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140572589,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs964306099"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572590,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140572590,"id":"rs1461938125","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572591,"feature_type":"variation","strand":1,"end":140572591,"alleles":["T","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1798137423"},{"strand":1,"feature_type":"variation","end":140572597,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572597,"source":"dbSNP","seq_region_name":"7","id":"rs1798137579","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1327270523","alleles":["T","A"],"end":140572601,"feature_type":"variation","strand":1,"source":"dbSNP","start":140572601,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["A","G"],"end":140572605,"feature_type":"variation","strand":1,"source":"dbSNP","start":140572605,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798137846"},{"seq_region_name":"7","id":"rs1798137974","clinical_significance":[],"strand":1,"feature_type":"variation","end":140572615,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572615,"source":"dbSNP"},{"seq_region_name":"7","id":"rs2130608654","clinical_significance":[],"end":140572616,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140572616,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs2130608668","seq_region_name":"7","alleles":["T","C"],"end":140572621,"feature_type":"variation","strand":1,"source":"dbSNP","start":140572621,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs2536954","clinical_significance":[],"alleles":["G","A","T"],"end":140572622,"strand":1,"feature_type":"variation","start":140572622,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572624,"source":"dbSNP","strand":1,"feature_type":"variation","end":140572624,"alleles":["G","T"],"id":"rs1462093371","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1031995062","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572625,"source":"dbSNP","strand":1,"feature_type":"variation","end":140572625,"alleles":["G","A"]},{"source":"dbSNP","start":140572628,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140572628,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs977279266"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572629,"feature_type":"variation","strand":1,"end":140572629,"alleles":["C","T"],"clinical_significance":[],"id":"rs1798138669","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572634,"feature_type":"variation","strand":1,"end":140572634,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1200233518"},{"alleles":["C","A","T"],"end":140572636,"feature_type":"variation","strand":1,"source":"dbSNP","start":140572636,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1798138924","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798139074","source":"dbSNP","start":140572642,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140572642,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572644,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140572644,"seq_region_name":"7","id":"rs1277236137","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572646,"feature_type":"variation","strand":1,"end":140572646,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1214677868"},{"id":"rs866423401","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572647,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140572647},{"clinical_significance":[],"seq_region_name":"7","id":"rs1329144204","alleles":["GGG","GG"],"end":140572649,"feature_type":"variation","strand":1,"source":"dbSNP","start":140572647,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs576040231","source":"dbSNP","start":140572649,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140572649,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs200839766","clinical_significance":[],"alleles":["T","C"],"end":140572654,"strand":1,"feature_type":"variation","start":140572654,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572657,"feature_type":"variation","strand":1,"end":140572657,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1798139938"},{"start":140572660,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140572660,"alleles":["A","G"],"strand":1,"feature_type":"variation","id":"rs1383337562","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798140126","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572662,"source":"dbSNP","strand":1,"feature_type":"variation","end":140572662,"alleles":["G","C"]},{"alleles":["A","G"],"end":140572663,"feature_type":"variation","strand":1,"source":"dbSNP","start":140572663,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585663692"},{"clinical_significance":[],"id":"rs1381271833","seq_region_name":"7","feature_type":"variation","strand":1,"end":140572664,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572664},{"seq_region_name":"7","id":"rs1585663700","clinical_significance":[],"alleles":["A","G"],"end":140572665,"strand":1,"feature_type":"variation","start":140572665,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs987888498","clinical_significance":[],"strand":1,"feature_type":"variation","end":140572668,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572668,"source":"dbSNP"},{"id":"rs1464773867","seq_region_name":"7","clinical_significance":[],"end":140572669,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140572669,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140572676,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572676,"source":"dbSNP","seq_region_name":"7","id":"rs1798140842","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572685,"feature_type":"variation","strand":1,"end":140572685,"alleles":["C","T"],"clinical_significance":[],"id":"rs1286889514","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs917637241","source":"dbSNP","start":140572686,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140572686,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572688,"source":"dbSNP","strand":1,"feature_type":"variation","end":140572688,"alleles":["A","G"],"seq_region_name":"7","id":"rs1798141195","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585663739","alleles":["A","G"],"end":140572689,"feature_type":"variation","strand":1,"source":"dbSNP","start":140572689,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140572697,"alleles":["AGTTGCAGT","AGTTGCAGTTGCAGT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572689,"clinical_significance":[],"seq_region_name":"7","id":"rs1798141408"},{"start":140572693,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140572693,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798141524","clinical_significance":[]},{"source":"dbSNP","start":140572694,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140572694,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798141621"},{"seq_region_name":"7","id":"rs1798141722","clinical_significance":[],"strand":1,"feature_type":"variation","end":140572696,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572696,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1585663744","clinical_significance":[],"strand":1,"feature_type":"variation","end":140572698,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572698,"source":"dbSNP"},{"start":140572699,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140572699,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs970549597","clinical_significance":[]},{"seq_region_name":"7","id":"rs1388846125","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140572702,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572702,"source":"dbSNP"},{"end":140572703,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140572703,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798142179","clinical_significance":[]},{"seq_region_name":"7","id":"rs1168588483","clinical_significance":[],"start":140572710,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140572710,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1798142406","clinical_significance":[],"start":140572712,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140572712,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140572717,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572717,"source":"dbSNP","seq_region_name":"7","id":"rs1798142519","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1275086405","feature_type":"variation","strand":1,"end":140572723,"alleles":["CTCC","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572720},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572721,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140572721,"seq_region_name":"7","id":"rs1445588160","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140572728,"alleles":["TCCAGCTT","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572721,"source":"dbSNP","seq_region_name":"7","id":"rs1798142879","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs533757729","source":"dbSNP","start":140572724,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AG","AGAG"],"end":140572725,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572727,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TT","TTT"],"end":140572728,"seq_region_name":"7","id":"rs1482047646","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585663812","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140572728,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572728},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798143325","source":"dbSNP","start":140572731,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140572731,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798143437","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572731,"feature_type":"variation","strand":1,"end":140572732,"alleles":["GC","-"]},{"feature_type":"variation","strand":1,"end":140572750,"alleles":["ACAGAGTGAAACTCTGT","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572734,"clinical_significance":[],"seq_region_name":"7","id":"rs1798143553"},{"seq_region_name":"7","id":"rs1236537010","clinical_significance":[],"strand":1,"feature_type":"variation","end":140572735,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572735,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572735,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CAGAGTGAAACTCTGTC","-"],"end":140572751,"seq_region_name":"7","id":"rs1798143769","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572737,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140572737,"seq_region_name":"7","id":"rs1798143890","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs549614421","feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140572738,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572738},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130609091","feature_type":"variation","strand":1,"end":140572739,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572739},{"end":140572741,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140572741,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1194207122","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798144269","clinical_significance":[],"end":140572743,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140572743,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs866911283","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572744,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140572744},{"strand":1,"feature_type":"variation","alleles":["CTCT","CT"],"end":140572748,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572745,"source":"dbSNP","seq_region_name":"7","id":"rs1798144494","clinical_significance":[]},{"clinical_significance":[],"id":"rs1798144611","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572747,"feature_type":"variation","strand":1,"end":140572747,"alleles":["C","T"]},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140572749,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572749,"clinical_significance":[],"seq_region_name":"7","id":"rs2130609131"},{"source":"dbSNP","start":140572750,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140572750,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1251504431"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1308807642","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572750,"feature_type":"variation","strand":1,"alleles":["T","-"],"end":140572750},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572751,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["-","A"],"end":140572750,"seq_region_name":"7","id":"rs1798144946","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1227619761","end":140572751,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140572751,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572751,"source":"dbSNP","strand":1,"feature_type":"variation","end":140572751,"alleles":["C","-"],"seq_region_name":"7","id":"rs1272379976","clinical_significance":[]},{"alleles":["CA","-"],"end":140572752,"feature_type":"variation","strand":1,"source":"dbSNP","start":140572751,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798145260"},{"seq_region_name":"7","id":"rs1798145363","clinical_significance":[],"alleles":["A","C"],"end":140572752,"strand":1,"feature_type":"variation","start":140572752,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["AAA","AAATAAA"],"end":140572754,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572752,"clinical_significance":[],"seq_region_name":"7","id":"rs1798145467"},{"alleles":["AAAAAAAAAAAAAAAAAAAAAA","AAAAAAAA","AAAAAAAAAA","AAAAAAAAAAA","AAAAAAAAAAAA","AAAAAAAAAAAAA","AAAAAAAAAAAAAA","AAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA"],"end":140572773,"feature_type":"variation","strand":1,"source":"dbSNP","start":140572752,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs59174097"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572753,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140572753,"seq_region_name":"7","id":"rs1168486517","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798147002","clinical_significance":[],"alleles":["A","C"],"end":140572755,"strand":1,"feature_type":"variation","start":140572755,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798147172","end":140572760,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140572760,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140572764,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140572764,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1798147349","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1798147495","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140572766,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572766,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140572769,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572769,"source":"dbSNP","seq_region_name":"7","id":"rs1798147678","clinical_significance":[]},{"id":"rs926543907","seq_region_name":"7","clinical_significance":[],"end":140572771,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140572771,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1798148038","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["AAGAAG","AAG"],"end":140572777,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572772,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798148215","feature_type":"variation","strand":1,"end":140572782,"alleles":["AAGAAGTTGAT","AAGAAGTTGATAAGAAGTTGAT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572772},{"clinical_significance":[],"seq_region_name":"7","id":"rs141500684","feature_type":"variation","strand":1,"end":140572774,"alleles":["G","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572774},{"seq_region_name":"7","id":"rs1419956781","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572774,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140572774},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140572775,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572775,"clinical_significance":[],"seq_region_name":"7","id":"rs1798148741"},{"clinical_significance":[],"id":"rs1798148893","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140572776,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572776},{"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140572780,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572780,"clinical_significance":[],"seq_region_name":"7","id":"rs1163037993"},{"id":"rs1798149267","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572781,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140572781},{"clinical_significance":[],"id":"rs2130609349","seq_region_name":"7","feature_type":"variation","strand":1,"end":140572783,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572783},{"seq_region_name":"7","id":"rs1798149443","clinical_significance":[],"start":140572786,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C","T"],"end":140572786,"strand":1,"feature_type":"variation"},{"end":140572792,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140572792,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs985642163","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585663974","clinical_significance":[],"start":140572793,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140572793,"alleles":["T","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1412603532","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572794,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140572794},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572795,"source":"dbSNP","strand":1,"feature_type":"variation","end":140572795,"alleles":["C","T"],"seq_region_name":"7","id":"rs1798150321","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1475470698","feature_type":"variation","strand":1,"end":140572798,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572798},{"clinical_significance":[],"seq_region_name":"7","id":"rs941945257","feature_type":"variation","strand":1,"end":140572799,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572799},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572800,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140572800,"clinical_significance":[],"seq_region_name":"7","id":"rs542916608"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140572801,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572801,"source":"dbSNP","seq_region_name":"7","id":"rs936263249","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798151245","clinical_significance":[],"start":140572802,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140572802,"alleles":["T","TT"],"strand":1,"feature_type":"variation"},{"start":140572808,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140572808,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798151349","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798151461","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572809,"source":"dbSNP","strand":1,"feature_type":"variation","end":140572811,"alleles":["CCA","CCACCA"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1203836255","feature_type":"variation","strand":1,"end":140572811,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572811},{"seq_region_name":"7","id":"rs755742346","clinical_significance":[],"strand":1,"feature_type":"variation","end":140572824,"alleles":["T","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572824,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1242329425","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140572832,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572832,"source":"dbSNP"},{"id":"rs1798151980","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572837,"source":"dbSNP","strand":1,"feature_type":"variation","end":140572837,"alleles":["T","G"]},{"seq_region_name":"7","id":"rs1320968330","clinical_significance":[],"strand":1,"feature_type":"variation","end":140572838,"alleles":["G","C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572838,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140572846,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572846,"source":"dbSNP","seq_region_name":"7","id":"rs2130609483","clinical_significance":[]},{"id":"rs1798152177","seq_region_name":"7","clinical_significance":[],"start":140572847,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140572847,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572854,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140572854,"clinical_significance":[],"seq_region_name":"7","id":"rs1563150724"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572855,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140572855,"clinical_significance":[],"seq_region_name":"7","id":"rs919936202"},{"start":140572857,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140572857,"strand":1,"feature_type":"variation","id":"rs2130609506","seq_region_name":"7","clinical_significance":[]},{"id":"rs2130609520","seq_region_name":"7","clinical_significance":[],"start":140572858,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140572858,"alleles":["T","G"],"strand":1,"feature_type":"variation"},{"start":140572863,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140572863,"alleles":["A","G"],"strand":1,"feature_type":"variation","id":"rs1798152501","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572864,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140572864,"seq_region_name":"7","id":"rs989050438","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585664103","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140572865,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572865,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs930095140","feature_type":"variation","strand":1,"end":140572870,"alleles":["G","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572870},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798153318","source":"dbSNP","start":140572871,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140572871,"alleles":["T","G"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140572872,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572872,"clinical_significance":[],"seq_region_name":"7","id":"rs1389370240"},{"clinical_significance":[],"id":"rs2130609573","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140572876,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572876},{"feature_type":"variation","strand":1,"end":140572881,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572881,"clinical_significance":[],"id":"rs1798153694","seq_region_name":"7"},{"end":140572882,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140572882,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs777904930","seq_region_name":"7"},{"start":140572883,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140572883,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs147879693","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798154273","source":"dbSNP","start":140572893,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140572893,"alleles":["T","A"],"feature_type":"variation","strand":1},{"alleles":["C","T"],"end":140572894,"strand":1,"feature_type":"variation","start":140572894,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1008370316","clinical_significance":[]},{"alleles":["C","T"],"end":140572895,"strand":1,"feature_type":"variation","start":140572895,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798154612","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1415867652","source":"dbSNP","start":140572897,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140572897,"alleles":["T","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1457714991","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572900,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140572900},{"clinical_significance":[],"id":"rs1798154908","seq_region_name":"7","alleles":["T","C"],"end":140572918,"feature_type":"variation","strand":1,"source":"dbSNP","start":140572918,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572922,"source":"dbSNP","strand":1,"feature_type":"variation","end":140572922,"alleles":["A","C"],"seq_region_name":"7","id":"rs571327013","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs945059316","alleles":["T","A","C"],"end":140572928,"feature_type":"variation","strand":1,"source":"dbSNP","start":140572928,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140572931,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572931,"source":"dbSNP","id":"rs1798155098","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140572931,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AAAAGA","A"],"end":140572936,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798155186"},{"id":"rs1798155283","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140572935,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572935,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1798155374","clinical_significance":[],"alleles":["A","C"],"end":140572936,"strand":1,"feature_type":"variation","start":140572936,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1320507334","source":"dbSNP","start":140572938,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C","T"],"end":140572938,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798155608","alleles":["C","G"],"end":140572939,"feature_type":"variation","strand":1,"source":"dbSNP","start":140572939,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1244113559","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140572940,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572940,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572945,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140572945,"clinical_significance":[],"id":"rs1409346529","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1798155904","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572947,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140572947},{"clinical_significance":[],"seq_region_name":"7","id":"rs1252013037","source":"dbSNP","start":140572948,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140572948,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572949,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140572949,"clinical_significance":[],"seq_region_name":"7","id":"rs185463686"},{"seq_region_name":"7","id":"rs1269375684","clinical_significance":[],"start":140572951,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140572951,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798156251","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572954,"feature_type":"variation","strand":1,"end":140572954,"alleles":["G","A","C"]},{"start":140572955,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140572955,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1208036904","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572958,"source":"dbSNP","strand":1,"feature_type":"variation","end":140572958,"alleles":["G","A"],"seq_region_name":"7","id":"rs2130609779","clinical_significance":[]},{"seq_region_name":"7","id":"rs1488023421","clinical_significance":[],"strand":1,"feature_type":"variation","end":140572959,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572959,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1798156577","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140572965,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572965,"source":"dbSNP"},{"end":140572970,"alleles":["ATTAT","AT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140572966,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1203317854"},{"seq_region_name":"7","id":"rs900114247","clinical_significance":[],"start":140572967,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140572967,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"alleles":["T","A","C"],"end":140572968,"strand":1,"feature_type":"variation","start":140572968,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs540812731","clinical_significance":[]},{"clinical_significance":[],"id":"rs1798157010","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572970,"feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140572970},{"end":140572973,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140572973,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1485883757"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1054906944","end":140572977,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140572977,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572978,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140572978,"id":"rs1798157400","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1224184035","clinical_significance":[],"end":140572983,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140572983,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["A","G"],"end":140572985,"feature_type":"variation","strand":1,"source":"dbSNP","start":140572985,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1001107053"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572992,"source":"dbSNP","strand":1,"feature_type":"variation","end":140572992,"alleles":["G","A"],"seq_region_name":"7","id":"rs1798157904","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798158012","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140572993,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572993},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140572997,"source":"dbSNP","strand":1,"feature_type":"variation","end":140572997,"alleles":["G","T"],"seq_region_name":"7","id":"rs1798158131","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs888266532","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140572999,"feature_type":"variation","strand":1,"alleles":["G","C","T"],"end":140572999},{"id":"rs1005458179","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140573001,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140573001,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798158531","source":"dbSNP","start":140573003,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140573003,"feature_type":"variation","strand":1},{"end":140573011,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140573011,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs749060509","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs559070135","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573013,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140573013},{"clinical_significance":[],"id":"rs532842853","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573016,"feature_type":"variation","strand":1,"end":140573016,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs1385980858","clinical_significance":[],"start":140573017,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140573017,"strand":1,"feature_type":"variation"},{"end":140573018,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140573018,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1158051845"},{"feature_type":"variation","strand":1,"end":140573019,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573019,"clinical_significance":[],"seq_region_name":"7","id":"rs1378908391"},{"id":"rs998202699","seq_region_name":"7","clinical_significance":[],"end":140573026,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140573026,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1193249686","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573028,"feature_type":"variation","strand":1,"end":140573028,"alleles":["C","G","T"]},{"source":"dbSNP","start":140573030,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140573030,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1030045372"},{"clinical_significance":[],"id":"rs1190202684","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573033,"feature_type":"variation","strand":1,"end":140573033,"alleles":["T","A"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573037,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140573037,"clinical_significance":[],"seq_region_name":"7","id":"rs1798159716"},{"seq_region_name":"7","id":"rs954176006","clinical_significance":[],"start":140573039,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140573039,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1267737470","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140573043,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573043},{"seq_region_name":"7","id":"rs1798160063","clinical_significance":[],"start":140573045,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140573045,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"start":140573049,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140573049,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs188707418","clinical_significance":[]},{"source":"dbSNP","start":140573054,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AA","A"],"end":140573055,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798160663"},{"seq_region_name":"7","id":"rs1798160787","clinical_significance":[],"start":140573055,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140573055,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130610005","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573056,"feature_type":"variation","strand":1,"end":140573057,"alleles":["TT","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1024745525","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573060,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140573060},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140573061,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573061,"clinical_significance":[],"seq_region_name":"7","id":"rs970435207"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1370280268","source":"dbSNP","start":140573069,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140573069,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1327460467","alleles":["C","A"],"end":140573071,"feature_type":"variation","strand":1,"source":"dbSNP","start":140573071,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1435717066","clinical_significance":[],"start":140573074,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140573074,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"end":140573078,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140573078,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798161438","clinical_significance":[]},{"clinical_significance":[],"id":"rs1433347129","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573079,"feature_type":"variation","strand":1,"end":140573079,"alleles":["T","C","G"]},{"clinical_significance":[],"id":"rs1364980052","seq_region_name":"7","feature_type":"variation","strand":1,"end":140573088,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573088},{"seq_region_name":"7","id":"rs778869050","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140573091,"source":"dbSNP","strand":1,"feature_type":"variation","end":140573091,"alleles":["T","A","C"]},{"alleles":["A","C","G"],"end":140573092,"feature_type":"variation","strand":1,"source":"dbSNP","start":140573092,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798161939"},{"start":140573094,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140573094,"alleles":["G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs115174616","clinical_significance":[]},{"seq_region_name":"7","id":"rs1403946217","clinical_significance":[],"start":140573098,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140573098,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs913488323","clinical_significance":[],"end":140573102,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140573102,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140573106,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G","T"],"end":140573106,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798162858","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573109,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140573109,"clinical_significance":[],"seq_region_name":"7","id":"rs1732695604"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140573118,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573118,"clinical_significance":[],"seq_region_name":"7","id":"rs115571725"},{"seq_region_name":"7","id":"rs139970682","clinical_significance":[],"strand":1,"feature_type":"variation","end":140573119,"alleles":["A","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140573119,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1296336017","clinical_significance":[],"start":140573120,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140573120,"alleles":["T","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798163312","source":"dbSNP","start":140573132,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140573132,"alleles":["G","T"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140573133,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573133,"clinical_significance":[],"id":"rs1798163435","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1328278895","feature_type":"variation","strand":1,"end":140573137,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573137},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140573139,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140573139,"id":"rs1798163658","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1447400605","source":"dbSNP","start":140573140,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140573140,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1247238759","end":140573141,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140573141,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573142,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140573142,"clinical_significance":[],"seq_region_name":"7","id":"rs927600694"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140573149,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573149,"clinical_significance":[],"seq_region_name":"7","id":"rs1798164121"},{"seq_region_name":"7","id":"rs1798164235","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140573152,"source":"dbSNP","strand":1,"feature_type":"variation","end":140573152,"alleles":["A","G"]},{"end":140573157,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140573157,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798164345"},{"start":140573160,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140573160,"alleles":["A","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1226383525","clinical_significance":[]},{"seq_region_name":"7","id":"rs1274173827","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140573168,"source":"dbSNP","strand":1,"feature_type":"variation","end":140573168,"alleles":["T","C"]},{"id":"rs1798164703","seq_region_name":"7","clinical_significance":[],"start":140573172,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140573172,"strand":1,"feature_type":"variation"},{"start":140573173,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140573173,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs74941501","clinical_significance":[]},{"source":"dbSNP","start":140573175,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140573175,"alleles":["T","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1212715358"},{"end":140573181,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140573181,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs919140885"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573183,"feature_type":"variation","strand":1,"end":140573183,"alleles":["T","A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1226909532"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573187,"feature_type":"variation","strand":1,"end":140573187,"alleles":["T","C"],"clinical_significance":[],"id":"rs771756906","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573188,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140573188,"clinical_significance":[],"id":"rs1798165355","seq_region_name":"7"},{"alleles":["C","T"],"end":140573190,"feature_type":"variation","strand":1,"source":"dbSNP","start":140573190,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1054793711"},{"start":140573191,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140573191,"strand":1,"feature_type":"variation","id":"rs2536955","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573193,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140573193,"clinical_significance":[],"seq_region_name":"7","id":"rs912660965"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1331854891","feature_type":"variation","strand":1,"end":140573195,"alleles":["G","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573195},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140573196,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140573196,"seq_region_name":"7","id":"rs1798166147","clinical_significance":[]},{"seq_region_name":"7","id":"rs1187070565","clinical_significance":[],"start":140573206,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140573206,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140573207,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573207,"clinical_significance":[],"seq_region_name":"7","id":"rs1263143537"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798166466","feature_type":"variation","strand":1,"end":140573222,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573222},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573227,"feature_type":"variation","strand":1,"end":140573227,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1798166586"},{"end":140573229,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140573229,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs944124192","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1396642006","end":140573230,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140573230,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573238,"feature_type":"variation","strand":1,"end":140573238,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1447150366"},{"start":140573243,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140573243,"alleles":["T","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1427682347","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798167155","end":140573251,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140573251,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140573253,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140573253,"source":"dbSNP","id":"rs1798167270","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798167393","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140573255,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140573255},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140573256,"source":"dbSNP","strand":1,"feature_type":"variation","end":140573256,"alleles":["A","G"],"seq_region_name":"7","id":"rs1389511263","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798167605","clinical_significance":[],"start":140573257,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["-","TAGGTAGG"],"end":140573256,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs74734231","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140573257,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573257},{"seq_region_name":"7","id":"rs115018973","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140573258,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140573258},{"clinical_significance":[],"seq_region_name":"7","id":"rs1366933189","source":"dbSNP","start":140573259,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140573259,"feature_type":"variation","strand":1},{"start":140573260,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140573260,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798168058","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798168160","source":"dbSNP","start":140573261,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140573261,"alleles":["A","C"],"feature_type":"variation","strand":1},{"end":140573266,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140573266,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1455342187","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140573267,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140573267,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1438448609"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798168484","alleles":["C","T"],"end":140573272,"feature_type":"variation","strand":1,"source":"dbSNP","start":140573272,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140573273,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573273,"clinical_significance":[],"seq_region_name":"7","id":"rs1798168586"},{"feature_type":"variation","strand":1,"end":140573274,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573274,"clinical_significance":[],"seq_region_name":"7","id":"rs1254014737"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798168792","source":"dbSNP","start":140573275,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140573275,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1798168908","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140573276,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140573276},{"strand":1,"feature_type":"variation","alleles":["AA","AAAA"],"end":140573278,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140573277,"source":"dbSNP","seq_region_name":"7","id":"rs1798169004","clinical_significance":[]},{"clinical_significance":[],"id":"rs1798169131","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573283,"feature_type":"variation","strand":1,"end":140573283,"alleles":["G","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs768430007","feature_type":"variation","strand":1,"alleles":["A","T"],"end":140573284,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573284},{"end":140573286,"alleles":["CC","CCC"],"strand":1,"feature_type":"variation","start":140573285,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1798169346","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","G"],"end":140573292,"strand":1,"feature_type":"variation","start":140573292,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798169461","clinical_significance":[]},{"source":"dbSNP","start":140573293,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140573293,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs936956319"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573296,"feature_type":"variation","strand":1,"end":140573296,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1054040659"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140573297,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140573297,"id":"rs1798169806","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1051128316","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140573299,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573299},{"end":140573300,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140573300,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1293158410","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573305,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140573305,"clinical_significance":[],"seq_region_name":"7","id":"rs1798170031"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140573308,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140573308,"id":"rs1798170137","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1798170246","seq_region_name":"7","alleles":["G","T"],"end":140573309,"feature_type":"variation","strand":1,"source":"dbSNP","start":140573309,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1798170349","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573311,"feature_type":"variation","strand":1,"end":140573311,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130610567","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573316,"feature_type":"variation","strand":1,"end":140573316,"alleles":["G","C"]},{"seq_region_name":"7","id":"rs892696514","clinical_significance":[],"start":140573332,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140573332,"alleles":["C","A","T"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573333,"feature_type":"variation","strand":1,"end":140573333,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1354766142"},{"source":"dbSNP","start":140573340,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140573340,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798170735"},{"strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140573341,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140573341,"source":"dbSNP","seq_region_name":"7","id":"rs539121119","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140573342,"source":"dbSNP","strand":1,"feature_type":"variation","end":140573342,"alleles":["T","A"],"id":"rs2130610618","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1024631525","alleles":["G","A"],"end":140573344,"feature_type":"variation","strand":1,"source":"dbSNP","start":140573344,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140573349,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140573349,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs73736617"},{"end":140573350,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140573350,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs625960"},{"seq_region_name":"7","id":"rs1585665002","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140573353,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140573353},{"end":140573355,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140573355,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs957404260","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","A","G"],"end":140573357,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573357,"clinical_significance":[],"seq_region_name":"7","id":"rs762342709"},{"id":"rs1798171881","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140573358,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140573358,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1798172001","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573360,"feature_type":"variation","strand":1,"end":140573360,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1033964033","source":"dbSNP","start":140573367,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140573367,"feature_type":"variation","strand":1},{"id":"rs971696521","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140573368,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140573368,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140573380,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TTTTT","TTTTTT"],"end":140573384,"seq_region_name":"7","id":"rs982087306","clinical_significance":[]},{"clinical_significance":[],"id":"rs1798172463","seq_region_name":"7","source":"dbSNP","start":140573383,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140573383,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1798172627","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140573384,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573384},{"clinical_significance":[],"seq_region_name":"7","id":"rs1432951020","source":"dbSNP","start":140573388,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140573388,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1297044498","clinical_significance":[],"end":140573394,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140573394,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1180033265","clinical_significance":[],"start":140573396,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140573396,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"alleles":["C","T"],"end":140573397,"feature_type":"variation","strand":1,"source":"dbSNP","start":140573397,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798173295"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140573398,"source":"dbSNP","strand":1,"feature_type":"variation","end":140573398,"alleles":["C","T"],"seq_region_name":"7","id":"rs2130610753","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140573399,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140573399,"source":"dbSNP","seq_region_name":"7","id":"rs1371983579","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798173548","clinical_significance":[],"strand":1,"feature_type":"variation","end":140573400,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140573400,"source":"dbSNP"},{"source":"dbSNP","start":140573401,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AA","AAA"],"end":140573402,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1472339892"},{"id":"rs1798173809","seq_region_name":"7","clinical_significance":[],"start":140573402,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140573402,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1270225740","clinical_significance":[],"start":140573404,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140573404,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130610800","feature_type":"variation","strand":1,"end":140573405,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573405},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140573408,"source":"dbSNP","strand":1,"feature_type":"variation","end":140573408,"alleles":["A","G"],"seq_region_name":"7","id":"rs1798174056","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140573409,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573409,"clinical_significance":[],"id":"rs1798174174","seq_region_name":"7"},{"alleles":["G","T"],"end":140573423,"strand":1,"feature_type":"variation","start":140573423,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs963250349","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140573426,"source":"dbSNP","strand":1,"feature_type":"variation","end":140573426,"alleles":["T","C"],"seq_region_name":"7","id":"rs1450213769","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1289551312","feature_type":"variation","strand":1,"end":140573444,"alleles":["ACAGACTGGGAC","AC"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573433},{"id":"rs973605760","seq_region_name":"7","clinical_significance":[],"start":140573436,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140573436,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585665164","source":"dbSNP","start":140573439,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140573439,"alleles":["T","G"],"feature_type":"variation","strand":1},{"alleles":["G","A"],"end":140573442,"feature_type":"variation","strand":1,"source":"dbSNP","start":140573442,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1798174888","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573443,"feature_type":"variation","strand":1,"end":140573443,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs895143342"},{"strand":1,"feature_type":"variation","end":140573444,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140573444,"source":"dbSNP","seq_region_name":"7","id":"rs1026207492","clinical_significance":[]},{"source":"dbSNP","start":140573445,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140573445,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs536956036"},{"strand":1,"feature_type":"variation","end":140573453,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140573453,"source":"dbSNP","id":"rs1798175317","seq_region_name":"7","clinical_significance":[]},{"end":140573456,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140573456,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1311420111","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140573457,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140573457,"seq_region_name":"7","id":"rs1226022490","clinical_significance":[]},{"id":"rs2130610898","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140573457,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CGGGTGTCG","CGGGTGTCGGGTGTCG"],"end":140573465},{"start":140573458,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140573458,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs950608545","clinical_significance":[]},{"alleles":["G","A"],"end":140573460,"feature_type":"variation","strand":1,"source":"dbSNP","start":140573460,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs982775264"},{"alleles":["T","G"],"end":140573461,"feature_type":"variation","strand":1,"source":"dbSNP","start":140573461,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585665217"},{"seq_region_name":"7","id":"rs1275350336","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140573462,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140573462,"source":"dbSNP"},{"source":"dbSNP","start":140573464,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140573464,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs912546544"},{"clinical_significance":[],"seq_region_name":"7","id":"rs944160608","end":140573465,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140573465,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1798176284","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140573467,"source":"dbSNP","strand":1,"feature_type":"variation","end":140573467,"alleles":["C","T"]},{"start":140573468,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140573468,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1463517348","clinical_significance":[]},{"end":140573469,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140573469,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1457586398"},{"start":140573474,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140573474,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798176600","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130610986","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573476,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140573476},{"seq_region_name":"7","id":"rs1798176708","clinical_significance":[],"alleles":["AGAG","AGAGAG"],"end":140573482,"strand":1,"feature_type":"variation","start":140573479,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1391091931","seq_region_name":"7","clinical_significance":[],"start":140573485,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140573485,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"alleles":["T","G"],"end":140573488,"feature_type":"variation","strand":1,"source":"dbSNP","start":140573488,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1798176942","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140573489,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140573489,"seq_region_name":"7","id":"rs1798177056","clinical_significance":[]},{"id":"rs1798177150","seq_region_name":"7","clinical_significance":[],"start":140573490,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140573490,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1798177260","seq_region_name":"7","source":"dbSNP","start":140573495,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140573495,"feature_type":"variation","strand":1},{"end":140573500,"alleles":["TCT","T"],"strand":1,"feature_type":"variation","start":140573498,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798177360","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798177485","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140573500,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140573500,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573503,"feature_type":"variation","strand":1,"end":140573503,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1207545658"},{"seq_region_name":"7","id":"rs975518111","clinical_significance":[],"alleles":["T","C"],"end":140573507,"strand":1,"feature_type":"variation","start":140573507,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140573509,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140573509,"source":"dbSNP","seq_region_name":"7","id":"rs1253101787","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","A","G","T"],"end":140573512,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573512,"clinical_significance":[],"id":"rs765536960","seq_region_name":"7"},{"alleles":["G","A"],"end":140573513,"feature_type":"variation","strand":1,"source":"dbSNP","start":140573513,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs555004018"},{"source":"dbSNP","start":140573515,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140573515,"alleles":["T","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1585665306","seq_region_name":"7"},{"source":"dbSNP","start":140573516,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140573516,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1563151125"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573517,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140573517,"clinical_significance":[],"seq_region_name":"7","id":"rs1585665325"},{"seq_region_name":"7","id":"rs1193012986","clinical_significance":[],"start":140573524,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140573524,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"end":140573525,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140573525,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585665338"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1477303299","source":"dbSNP","start":140573526,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140573526,"alleles":["G","T"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140573530,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140573530,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585665358"},{"start":140573533,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140573533,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs1585665366","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573540,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140573540,"clinical_significance":[],"id":"rs1585665380","seq_region_name":"7"},{"alleles":["G","A"],"end":140573541,"feature_type":"variation","strand":1,"source":"dbSNP","start":140573541,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1798179282","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140573542,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140573542,"seq_region_name":"7","id":"rs536749753","clinical_significance":[]},{"clinical_significance":[],"id":"rs1462696463","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573545,"feature_type":"variation","strand":1,"end":140573545,"alleles":["A","C","G"]},{"alleles":["G","T"],"end":140573547,"strand":1,"feature_type":"variation","start":140573547,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585665408","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798179757","feature_type":"variation","strand":1,"end":140573550,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573550},{"start":140573551,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140573551,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs936871221","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140573554,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140573554,"source":"dbSNP","seq_region_name":"7","id":"rs1798179960","clinical_significance":[]},{"id":"rs80095915","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140573557,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140573557,"source":"dbSNP"},{"seq_region_name":"7","id":"rs933954150","clinical_significance":[],"alleles":["G","C","T"],"end":140573560,"strand":1,"feature_type":"variation","start":140573560,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs540498247","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140573564,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573564},{"clinical_significance":[],"seq_region_name":"7","id":"rs945591185","source":"dbSNP","start":140573566,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140573566,"alleles":["G","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1046135012","feature_type":"variation","strand":1,"end":140573579,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573579},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140573581,"source":"dbSNP","strand":1,"feature_type":"variation","end":140573581,"alleles":["T","C"],"seq_region_name":"7","id":"rs1798180696","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140573587,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140573587,"seq_region_name":"7","id":"rs181488902","clinical_significance":[]},{"id":"rs1798180933","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140573588,"source":"dbSNP","strand":1,"feature_type":"variation","end":140573590,"alleles":["GGG","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs906189931","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573590,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140573590},{"id":"rs1798181131","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140573594,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140573594,"source":"dbSNP"},{"alleles":["G","A"],"end":140573595,"feature_type":"variation","strand":1,"source":"dbSNP","start":140573595,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1002243492"},{"seq_region_name":"7","id":"rs1798181354","clinical_significance":[],"start":140573596,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140573596,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1033436837","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573597,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140573597},{"seq_region_name":"7","id":"rs1563151167","clinical_significance":[],"start":140573601,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140573601,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140573606,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140573606,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs898887540","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1395315996","clinical_significance":[],"start":140573611,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C"],"end":140573611,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798181991","feature_type":"variation","strand":1,"end":140573612,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573612},{"clinical_significance":[],"seq_region_name":"7","id":"rs1367143301","alleles":["C","T"],"end":140573614,"feature_type":"variation","strand":1,"source":"dbSNP","start":140573614,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1318757508","source":"dbSNP","start":140573616,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140573616,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs750800677","clinical_significance":[],"alleles":["A","G"],"end":140573617,"strand":1,"feature_type":"variation","start":140573617,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1359998598","clinical_significance":[],"end":140573622,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140573622,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1178237433","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["AAAAA","AAAA"],"end":140573629,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140573625,"source":"dbSNP"},{"end":140573626,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140573626,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1412845692"},{"strand":1,"feature_type":"variation","end":140573631,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140573631,"source":"dbSNP","id":"rs1425061488","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140573636,"source":"dbSNP","strand":1,"feature_type":"variation","end":140573636,"alleles":["G","A","T"],"seq_region_name":"7","id":"rs893238857","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798183039","source":"dbSNP","start":140573639,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140573639,"alleles":["C","T"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140573640,"source":"dbSNP","strand":1,"feature_type":"variation","end":140573640,"alleles":["G","A"],"seq_region_name":"7","id":"rs1451696127","clinical_significance":[]},{"seq_region_name":"7","id":"rs201827526","clinical_significance":[],"start":140573641,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AA","A"],"end":140573642,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1798183397","clinical_significance":[],"start":140573643,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140573643,"strand":1,"feature_type":"variation"},{"alleles":["G","A"],"end":140573644,"feature_type":"variation","strand":1,"source":"dbSNP","start":140573644,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798183508"},{"seq_region_name":"7","id":"rs1188369255","clinical_significance":[],"start":140573647,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140573647,"strand":1,"feature_type":"variation"},{"end":140573648,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140573648,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs994693706"},{"strand":1,"feature_type":"variation","end":140573649,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140573649,"source":"dbSNP","id":"rs1798183830","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798183945","clinical_significance":[],"strand":1,"feature_type":"variation","end":140573655,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140573655,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs577332342","end":140573656,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140573656,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140573661,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140573661,"seq_region_name":"7","id":"rs1211603203","clinical_significance":[]},{"start":140573662,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140573662,"alleles":["G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798184313","clinical_significance":[]},{"start":140573663,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140573663,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798184429","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140573671,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573671,"clinical_significance":[],"seq_region_name":"7","id":"rs950660106"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573672,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140573672,"clinical_significance":[],"seq_region_name":"7","id":"rs544673801"},{"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140573674,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573674,"clinical_significance":[],"seq_region_name":"7","id":"rs1798184702"},{"clinical_significance":[],"seq_region_name":"7","id":"rs763020174","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140573678,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573678},{"seq_region_name":"7","id":"rs1798184898","clinical_significance":[],"start":140573686,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140573686,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"end":140573695,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140573695,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs185985839"},{"seq_region_name":"7","id":"rs1798185133","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140573696,"source":"dbSNP","strand":1,"feature_type":"variation","end":140573696,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798185227","alleles":["A","C"],"end":140573697,"feature_type":"variation","strand":1,"source":"dbSNP","start":140573697,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140573703,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140573703,"source":"dbSNP","seq_region_name":"7","id":"rs1798185346","clinical_significance":[]},{"alleles":["G","A"],"end":140573704,"feature_type":"variation","strand":1,"source":"dbSNP","start":140573704,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs530388654","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585665708","end":140573711,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140573711,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1019609466","source":"dbSNP","start":140573712,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140573712,"alleles":["G","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1295073108","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573715,"feature_type":"variation","strand":1,"end":140573715,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs1585665726","clinical_significance":[],"strand":1,"feature_type":"variation","end":140573717,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140573717,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140573719,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140573719,"seq_region_name":"7","id":"rs1273229897","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1469438461","end":140573721,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140573721,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs766692245","source":"dbSNP","start":140573722,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140573722,"alleles":["T","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1380086673","clinical_significance":[],"start":140573723,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140573723,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["CTCC","C"],"end":140573729,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140573726,"source":"dbSNP","seq_region_name":"7","id":"rs1798187961","clinical_significance":[]},{"seq_region_name":"7","id":"rs1304869681","clinical_significance":[],"end":140573727,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140573727,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1034566406","seq_region_name":"7","clinical_significance":[],"start":140573728,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140573728,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs751568160","source":"dbSNP","start":140573732,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140573732,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1432128004","source":"dbSNP","start":140573738,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140573738,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140573744,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573744,"clinical_significance":[],"seq_region_name":"7","id":"rs990457219"},{"seq_region_name":"7","id":"rs975794510","clinical_significance":[],"start":140573745,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140573745,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798188915","source":"dbSNP","start":140573746,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140573746,"feature_type":"variation","strand":1},{"id":"rs377367999","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140573747,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140573747,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798189150","source":"dbSNP","start":140573750,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140573756,"alleles":["TTCTTTC","TTC"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs778897934","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140573758,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140573758,"source":"dbSNP"},{"seq_region_name":"7","id":"rs2130611715","clinical_significance":[],"start":140573765,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["GGGG","GGG"],"end":140573768,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs752788795","clinical_significance":[],"start":140573766,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140573766,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs372304281","clinical_significance":[],"strand":1,"feature_type":"variation","end":140573772,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140573772,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140573773,"source":"dbSNP","strand":1,"feature_type":"variation","end":140573773,"alleles":["G","C"],"id":"rs1798189607","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140573774,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140573774,"seq_region_name":"7","id":"rs1429080330","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs376713805","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573775,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140573775},{"clinical_significance":[],"seq_region_name":"7","id":"rs1481975466","source":"dbSNP","start":140573776,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140573776,"alleles":["T","C"],"feature_type":"variation","strand":1},{"id":"rs1585665894","seq_region_name":"7","clinical_significance":[],"start":140573777,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140573777,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140573781,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573781,"clinical_significance":[],"id":"rs1269909981","seq_region_name":"7"},{"seq_region_name":"7","id":"rs755123375","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140573784,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140573784},{"clinical_significance":[],"seq_region_name":"7","id":"rs780989068","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573785,"feature_type":"variation","strand":1,"end":140573785,"alleles":["A","T"]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140573786,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573786,"clinical_significance":[],"seq_region_name":"7","id":"rs867837582"},{"source":"dbSNP","start":140573790,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140573790,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585665929"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140573800,"assembly_name":"GRCh38","consequence_type":"splice_region_variant","start":140573800,"source":"dbSNP","seq_region_name":"7","id":"rs1798190737","clinical_significance":[]},{"seq_region_name":"7","id":"rs1236330092","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"splice_donor_region_variant","start":140573805,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140573805},{"alleles":["A","C"],"end":140573806,"feature_type":"variation","strand":1,"source":"dbSNP","start":140573806,"consequence_type":"splice_donor_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585665950"},{"clinical_significance":[],"id":"rs542601234","seq_region_name":"7","end":140573811,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140573811,"consequence_type":"synonymous_variant","assembly_name":"GRCh38"},{"id":"rs1798191163","seq_region_name":"7","clinical_significance":[],"start":140573812,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140573812,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"start":140573815,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["A","G"],"end":140573815,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs745856203","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140573818,"source":"dbSNP","strand":1,"feature_type":"variation","end":140573818,"alleles":["T","C"],"seq_region_name":"7","id":"rs1483954694","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140573821,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573821,"clinical_significance":[],"seq_region_name":"7","id":"rs1798191406"},{"start":140573824,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140573824,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798191504","clinical_significance":[]},{"alleles":["T","A"],"end":140573827,"feature_type":"variation","strand":1,"source":"dbSNP","start":140573827,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs529189553"},{"seq_region_name":"7","id":"rs780016985","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140573828,"source":"dbSNP","strand":1,"feature_type":"variation","end":140573828,"alleles":["T","C"]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140573829,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573829,"clinical_significance":[],"id":"rs1202444186","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140573833,"alleles":["C","T"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573833,"clinical_significance":[],"seq_region_name":"7","id":"rs748909329"},{"source":"dbSNP","start":140573834,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140573834,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":["uncertain significance"],"seq_region_name":"7","id":"rs768423577"},{"clinical_significance":[],"seq_region_name":"7","id":"rs370028328","feature_type":"variation","strand":1,"end":140573835,"alleles":["G","A"],"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573835},{"start":140573842,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["G","A"],"end":140573842,"strand":1,"feature_type":"variation","id":"rs761212767","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140573845,"alleles":["T","A"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573845,"clinical_significance":[],"id":"rs914069490","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140573846,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140573846,"seq_region_name":"7","id":"rs550598136","clinical_significance":[]},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573848,"feature_type":"variation","strand":1,"end":140573848,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs773572471"},{"alleles":["C","T"],"end":140573849,"strand":1,"feature_type":"variation","start":140573849,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs761269555","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1285611060","alleles":["A","G"],"end":140573850,"feature_type":"variation","strand":1,"source":"dbSNP","start":140573850,"consequence_type":"synonymous_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1244623881","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573851,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140573851},{"start":140573853,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["G","A","T"],"end":140573853,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs766616206","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798193363","end":140573858,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140573858,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140573859,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140573859,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs754210561"},{"alleles":["AAAA","AAAAA"],"end":140573863,"strand":1,"feature_type":"variation","start":140573860,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"frameshift_variant","seq_region_name":"7","id":"rs1563151407","clinical_significance":[]},{"seq_region_name":"7","id":"rs1159937960","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140573865,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140573865},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798193837","source":"dbSNP","start":140573867,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140573867,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1445459894","seq_region_name":"7","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573870,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140573870},{"seq_region_name":"7","id":"rs759697166","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140573877,"source":"dbSNP","strand":1,"feature_type":"variation","end":140573877,"alleles":["G","T"]},{"id":"rs765433912","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140573882,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140573882,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140573883,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140573883,"id":"rs1798194393","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798194537","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573884,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140573884},{"end":140573885,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140573885,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","id":"rs1798194663","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs528367786","seq_region_name":"7","source":"dbSNP","start":140573886,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","end":140573886,"alleles":["G","T"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140573888,"source":"dbSNP","strand":1,"feature_type":"variation","end":140573888,"alleles":["A","T"],"seq_region_name":"7","id":"rs1332089428","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1407119749","alleles":["G","A"],"end":140573889,"feature_type":"variation","strand":1,"source":"dbSNP","start":140573889,"consequence_type":"synonymous_variant","assembly_name":"GRCh38"},{"alleles":["G","A"],"end":140573891,"strand":1,"feature_type":"variation","start":140573891,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs758379379","clinical_significance":[]},{"source":"dbSNP","start":140573892,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","end":140573892,"alleles":["A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs764281412","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs972883193","alleles":["G","C"],"end":140573894,"feature_type":"variation","strand":1,"source":"dbSNP","start":140573894,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1798195555","clinical_significance":[],"start":140573895,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","alleles":["G","A"],"end":140573895,"strand":1,"feature_type":"variation"},{"start":140573898,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","alleles":["G","A"],"end":140573898,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs750277848","clinical_significance":[]},{"alleles":["T","C"],"end":140573903,"strand":1,"feature_type":"variation","start":140573903,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs2130612123","clinical_significance":[]},{"source":"dbSNP","start":140573904,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","end":140573904,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs2130612132","seq_region_name":"7"},{"id":"rs756107778","seq_region_name":"7","clinical_significance":["uncertain significance"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140573911,"source":"dbSNP","strand":1,"feature_type":"variation","end":140573911,"alleles":["G","A"]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140573913,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573913,"clinical_significance":[],"seq_region_name":"7","id":"rs753779299"},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573915,"feature_type":"variation","strand":1,"end":140573915,"alleles":["C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1411756203"},{"clinical_significance":[],"seq_region_name":"7","id":"rs779927314","consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573916,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140573916},{"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140573919,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140573919,"seq_region_name":"7","id":"rs937710801","clinical_significance":[]},{"start":140573923,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140573923,"alleles":["T","G"],"strand":1,"feature_type":"variation","id":"rs749104629","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140573924,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140573924,"seq_region_name":"7","id":"rs1798196593","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs191980596","source":"dbSNP","start":140573925,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","end":140573925,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs778701152","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140573926,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140573926},{"strand":1,"feature_type":"variation","end":140573927,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140573927,"source":"dbSNP","seq_region_name":"7","id":"rs933817536","clinical_significance":[]},{"alleles":["A","C"],"end":140573928,"strand":1,"feature_type":"variation","start":140573928,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","id":"rs373075745","seq_region_name":"7","clinical_significance":["uncertain significance"]},{"source":"dbSNP","start":140573932,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140573932,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798197150"},{"end":140573937,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140573937,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs771437260","clinical_significance":[]},{"source":"dbSNP","start":140573938,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140573938,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798197421"},{"alleles":["T","C"],"end":140573939,"strand":1,"feature_type":"variation","start":140573939,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs1798197534","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140573941,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140573941,"source":"dbSNP","seq_region_name":"7","id":"rs375009610","clinical_significance":["uncertain significance"]},{"strand":1,"feature_type":"variation","end":140573942,"alleles":["T","C","G"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140573942,"source":"dbSNP","seq_region_name":"7","id":"rs1798197826","clinical_significance":[]},{"start":140573947,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["A","C","G"],"end":140573947,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs200365236","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140573948,"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140573948,"source":"dbSNP","id":"rs1158256201","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140573949,"alleles":["C","A","G"],"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573949,"clinical_significance":[],"seq_region_name":"7","id":"rs771441073"},{"clinical_significance":["uncertain significance"],"seq_region_name":"7","id":"rs777180623","end":140573951,"alleles":["G","A","C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140573951,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"id":"rs1798198838","seq_region_name":"7","clinical_significance":[],"start":140573956,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"frameshift_variant","alleles":["AA","A"],"end":140573957,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140573958,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573958,"clinical_significance":[],"seq_region_name":"7","id":"rs1301620600"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140573961,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573961,"clinical_significance":[],"seq_region_name":"7","id":"rs765632736"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1182191916","source":"dbSNP","start":140573964,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140573964,"alleles":["C","G"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140573967,"source":"dbSNP","strand":1,"feature_type":"variation","end":140573967,"alleles":["C","T"],"seq_region_name":"7","id":"rs1411045456","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798200016","source":"dbSNP","start":140573969,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140573969,"alleles":["C","G"],"feature_type":"variation","strand":1},{"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573970,"feature_type":"variation","strand":1,"end":140573970,"alleles":["T","C"],"clinical_significance":[],"id":"rs775550502","seq_region_name":"7"},{"consequence_type":"frameshift_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573974,"feature_type":"variation","strand":1,"end":140573977,"alleles":["TTTT","TTT"],"clinical_significance":[],"seq_region_name":"7","id":"rs1798200296"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798200448","feature_type":"variation","strand":1,"end":140573976,"alleles":["T","G"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573976},{"feature_type":"variation","strand":1,"end":140573977,"alleles":["T","C"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573977,"clinical_significance":[],"seq_region_name":"7","id":"rs200748334"},{"source":"dbSNP","start":140573980,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140573980,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":["uncertain significance"],"seq_region_name":"7","id":"rs764039930"},{"clinical_significance":[],"seq_region_name":"7","id":"rs372731585","consequence_type":"stop_gained","assembly_name":"GRCh38","source":"dbSNP","start":140573981,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140573981},{"seq_region_name":"7","id":"rs1798200976","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140573983,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140573983},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798201098","end":140573988,"alleles":["AAAAAA","AAAAAAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140573983,"consequence_type":"frameshift_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1266949442","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140573984,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140573984,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798201341","end":140573985,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140573985,"consequence_type":"synonymous_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140573986,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140573986,"source":"dbSNP","seq_region_name":"7","id":"rs1798201477","clinical_significance":[]},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140573989,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140573989,"clinical_significance":["uncertain significance"],"seq_region_name":"7","id":"rs201197656"},{"seq_region_name":"7","id":"rs766403215","clinical_significance":[],"end":140573990,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140573990,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"start":140573991,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","end":140573991,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585666659","clinical_significance":[]},{"end":140573996,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140573996,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","id":"rs753890167","seq_region_name":"7","clinical_significance":[]},{"id":"rs754786440","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140573998,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140573998,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798202227","source":"dbSNP","start":140574001,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140574001,"alleles":["A","C"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"splice_acceptor_variant","start":140574007,"source":"dbSNP","strand":1,"feature_type":"variation","end":140574007,"alleles":["T","C"],"seq_region_name":"7","id":"rs778875168","clinical_significance":[]},{"seq_region_name":"7","id":"rs2486188533","clinical_significance":["uncertain significance"],"strand":1,"feature_type":"variation","end":140574008,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140574008,"source":"ClinVar"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563151695","feature_type":"variation","strand":1,"end":140574012,"alleles":["T","A"],"consequence_type":"splice_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574012},{"seq_region_name":"7","id":"rs1252542042","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140574013,"assembly_name":"GRCh38","consequence_type":"splice_region_variant","start":140574013,"source":"dbSNP"},{"alleles":["A","G"],"end":140574015,"feature_type":"variation","strand":1,"source":"dbSNP","start":140574015,"consequence_type":"splice_region_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130612513"},{"clinical_significance":[],"seq_region_name":"7","id":"rs747718646","consequence_type":"splice_polypyrimidine_tract_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574017,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140574017},{"end":140574021,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140574021,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_polypyrimidine_tract_variant","id":"rs2130612524","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140574022,"alleles":["G","C"],"consequence_type":"splice_polypyrimidine_tract_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574022,"clinical_significance":[],"id":"rs1321288252","seq_region_name":"7"},{"seq_region_name":"7","id":"rs758078198","clinical_significance":[],"start":140574024,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_polypyrimidine_tract_variant","end":140574024,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"start":140574026,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140574026,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs777093287","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140574028,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574028,"source":"dbSNP","seq_region_name":"7","id":"rs2130612547","clinical_significance":[]},{"seq_region_name":"7","id":"rs10274629","clinical_significance":[],"start":140574031,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140574031,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140574035,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140574035,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1348754819"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574036,"feature_type":"variation","strand":1,"end":140574036,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130612566"},{"alleles":["T","G"],"end":140574045,"strand":1,"feature_type":"variation","start":140574045,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs946186450","seq_region_name":"7","clinical_significance":[]},{"start":140574046,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140574046,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1161896056","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574056,"feature_type":"variation","strand":1,"end":140574056,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1798203593"},{"clinical_significance":[],"seq_region_name":"7","id":"rs529375462","end":140574057,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140574057,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs777092667","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","A","G","T"],"end":140574060,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574060},{"seq_region_name":"7","id":"rs373798035","clinical_significance":[],"end":140574061,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140574061,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs536296377","clinical_significance":[],"alleles":["G","T"],"end":140574062,"strand":1,"feature_type":"variation","start":140574062,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574064,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140574064,"seq_region_name":"7","id":"rs377407414","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574071,"feature_type":"variation","strand":1,"end":140574071,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585666880"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1393261311","source":"dbSNP","start":140574078,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140574078,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1798204838","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574084,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140574084},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574085,"feature_type":"variation","strand":1,"end":140574085,"alleles":["A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1159529604"},{"end":140574086,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140574086,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1288599654"},{"clinical_significance":[],"seq_region_name":"7","id":"rs966869595","source":"dbSNP","start":140574087,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140574087,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs6964982","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574091,"feature_type":"variation","strand":1,"end":140574091,"alleles":["C","A","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798205528","end":140574098,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140574098,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574105,"source":"dbSNP","strand":1,"feature_type":"variation","end":140574105,"alleles":["A","C"],"seq_region_name":"7","id":"rs1433634989","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130612684","feature_type":"variation","strand":1,"end":140574107,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574107},{"clinical_significance":[],"id":"rs1798205747","seq_region_name":"7","source":"dbSNP","start":140574114,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140574114,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798205853","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140574118,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574118},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574118,"feature_type":"variation","strand":1,"alleles":["TATGT","TATGTATGT"],"end":140574122,"clinical_significance":[],"seq_region_name":"7","id":"rs1798205974"},{"seq_region_name":"7","id":"rs1798206107","clinical_significance":[],"alleles":["A","G"],"end":140574119,"strand":1,"feature_type":"variation","start":140574119,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140574122,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574122,"clinical_significance":[],"id":"rs758570769","seq_region_name":"7"},{"start":140574124,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140574124,"alleles":["C","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs894747088","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140574133,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574133,"clinical_significance":[],"seq_region_name":"7","id":"rs1798206465"},{"id":"rs1798206592","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574135,"source":"dbSNP","strand":1,"feature_type":"variation","end":140574135,"alleles":["T","C"]},{"start":140574137,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140574137,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585666986","clinical_significance":[]},{"seq_region_name":"7","id":"rs1189235600","clinical_significance":[],"strand":1,"feature_type":"variation","end":140574138,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574138,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1467922315","seq_region_name":"7","end":140574139,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140574139,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1248850673","seq_region_name":"7","clinical_significance":[],"start":140574146,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140574146,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1798207141","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","A"],"end":140574154,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574154},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574154,"feature_type":"variation","strand":1,"alleles":["T","TT"],"end":140574154,"clinical_significance":[],"seq_region_name":"7","id":"rs1798207243"},{"seq_region_name":"7","id":"rs1798207371","clinical_significance":[],"strand":1,"feature_type":"variation","end":140574155,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574155,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140574160,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574160,"source":"dbSNP","id":"rs1210878646","seq_region_name":"7","clinical_significance":[]},{"id":"rs1798207602","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574163,"source":"dbSNP","strand":1,"feature_type":"variation","end":140574163,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs1482290110","clinical_significance":[],"start":140574164,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140574164,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1798207819","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574165,"source":"dbSNP","strand":1,"feature_type":"variation","end":140574165,"alleles":["T","C"]},{"source":"dbSNP","start":140574166,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140574166,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1798207910","seq_region_name":"7"},{"id":"rs60847193","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574170,"source":"dbSNP","strand":1,"feature_type":"variation","end":140574170,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798208189","feature_type":"variation","strand":1,"end":140574171,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574171},{"clinical_significance":[],"id":"rs2130612810","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574172,"feature_type":"variation","strand":1,"end":140574172,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs938250395","clinical_significance":[],"strand":1,"feature_type":"variation","end":140574173,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574173,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798208410","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140574180,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574180},{"clinical_significance":[],"id":"rs1054823333","seq_region_name":"7","feature_type":"variation","strand":1,"end":140574182,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574182},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798208619","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140574183,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574183},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140574189,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574189,"source":"dbSNP","seq_region_name":"7","id":"rs1798208755","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1299886797","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140574192,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574192},{"id":"rs962687043","seq_region_name":"7","clinical_significance":[],"start":140574195,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140574195,"alleles":["T","A","C"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574196,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140574196,"id":"rs1798209140","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1474095256","clinical_significance":[],"start":140574197,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140574197,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140574202,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140574202,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798209377"},{"seq_region_name":"7","id":"rs1366425501","clinical_significance":[],"strand":1,"feature_type":"variation","end":140574203,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574203,"source":"dbSNP"},{"alleles":["G","A"],"end":140574205,"feature_type":"variation","strand":1,"source":"dbSNP","start":140574205,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130612891"},{"seq_region_name":"7","id":"rs534470054","clinical_significance":[],"strand":1,"feature_type":"variation","end":140574206,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574206,"source":"dbSNP"},{"clinical_significance":[],"id":"rs558746175","seq_region_name":"7","alleles":["G","A"],"end":140574207,"feature_type":"variation","strand":1,"source":"dbSNP","start":140574207,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1047479010","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140574209,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574209,"source":"dbSNP"},{"id":"rs1798209975","seq_region_name":"7","clinical_significance":[],"alleles":["A","C"],"end":140574214,"strand":1,"feature_type":"variation","start":140574214,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs11983453","clinical_significance":[],"alleles":["T","C"],"end":140574221,"strand":1,"feature_type":"variation","start":140574221,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs986645129","end":140574223,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140574223,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1466157000","feature_type":"variation","strand":1,"end":140574231,"alleles":["TTTCTTT","TTT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574225},{"id":"rs768118301","seq_region_name":"7","clinical_significance":[],"start":140574229,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140574229,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574229,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TTTTTTTT","TTTTTTT","TTTTTTTTT"],"end":140574236,"seq_region_name":"7","id":"rs1170742498","clinical_significance":[]},{"start":140574231,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140574231,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs1369003361","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","A"],"end":140574239,"feature_type":"variation","strand":1,"source":"dbSNP","start":140574239,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1798210630","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574242,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140574242,"clinical_significance":[],"seq_region_name":"7","id":"rs2130612998"},{"alleles":["A","C","G"],"end":140574245,"feature_type":"variation","strand":1,"source":"dbSNP","start":140574245,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1040596119"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574251,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140574251,"seq_region_name":"7","id":"rs900437878","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798211000","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140574253,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574253},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140574254,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574254,"source":"dbSNP","seq_region_name":"7","id":"rs1798211211","clinical_significance":[]},{"seq_region_name":"7","id":"rs145326901","clinical_significance":[],"alleles":["C","T"],"end":140574261,"strand":1,"feature_type":"variation","start":140574261,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1390508306","alleles":["G","A"],"end":140574262,"feature_type":"variation","strand":1,"source":"dbSNP","start":140574262,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574264,"source":"dbSNP","strand":1,"feature_type":"variation","end":140574264,"alleles":["G","C"],"seq_region_name":"7","id":"rs556682142","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140574272,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574272,"source":"dbSNP","id":"rs1798211813","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130613052","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140574273,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574273,"source":"dbSNP"},{"clinical_significance":[],"id":"rs674866","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140574275,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574275},{"seq_region_name":"7","id":"rs1463656307","clinical_significance":[],"start":140574276,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140574276,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1798212520","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574279,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140574279},{"end":140574280,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140574280,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs542288400","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1010873216","alleles":["C","T"],"end":140574281,"feature_type":"variation","strand":1,"source":"dbSNP","start":140574281,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs914614789","seq_region_name":"7","clinical_significance":[],"start":140574282,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C"],"end":140574282,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140574290,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140574290,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130613128"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140574292,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574292,"source":"dbSNP","seq_region_name":"7","id":"rs1798213040","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574293,"feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140574293,"clinical_significance":[],"seq_region_name":"7","id":"rs946040481"},{"source":"dbSNP","start":140574294,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140574294,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798213292"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574295,"source":"dbSNP","strand":1,"feature_type":"variation","end":140574295,"alleles":["T","C"],"seq_region_name":"7","id":"rs1798213416","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130613170","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574297,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140574297},{"id":"rs1343524332","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574304,"source":"dbSNP","strand":1,"feature_type":"variation","end":140574304,"alleles":["C","T"]},{"clinical_significance":[],"id":"rs1021068863","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574305,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140574305},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140574307,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574307,"clinical_significance":[],"seq_region_name":"7","id":"rs1798213771"},{"seq_region_name":"7","id":"rs1798213890","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574311,"source":"dbSNP","strand":1,"feature_type":"variation","end":140574311,"alleles":["T","A"]},{"seq_region_name":"7","id":"rs1798213996","clinical_significance":[],"strand":1,"feature_type":"variation","end":140574312,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574312,"source":"dbSNP"},{"clinical_significance":[],"id":"rs770290293","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574313,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140574313},{"clinical_significance":[],"id":"rs1798214260","seq_region_name":"7","alleles":["A","G"],"end":140574319,"feature_type":"variation","strand":1,"source":"dbSNP","start":140574319,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574320,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140574320,"clinical_significance":[],"seq_region_name":"7","id":"rs1798214373"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1230093557","feature_type":"variation","strand":1,"end":140574321,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574321},{"seq_region_name":"7","id":"rs1798214620","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574326,"source":"dbSNP","strand":1,"feature_type":"variation","end":140574326,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1226668883","alleles":["C","T"],"end":140574328,"feature_type":"variation","strand":1,"source":"dbSNP","start":140574328,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs928722610","clinical_significance":[],"alleles":["C","T"],"end":140574333,"strand":1,"feature_type":"variation","start":140574333,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1317282414","source":"dbSNP","start":140574335,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140574335,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798215036","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574339,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140574339},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140574343,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574343,"source":"dbSNP","seq_region_name":"7","id":"rs1272011546","clinical_significance":[]},{"alleles":["G","A","C","T"],"end":140574344,"strand":1,"feature_type":"variation","start":140574344,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585667426","clinical_significance":[]},{"start":140574350,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G","T"],"end":140574350,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs966756460","clinical_significance":[]},{"seq_region_name":"7","id":"rs938753782","clinical_significance":[],"end":140574352,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140574352,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1798215777","seq_region_name":"7","source":"dbSNP","start":140574354,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140574354,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574355,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140574355,"clinical_significance":[],"seq_region_name":"7","id":"rs982305743"},{"clinical_significance":[],"seq_region_name":"7","id":"rs928104582","source":"dbSNP","start":140574356,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140574356,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1204878318","seq_region_name":"7","end":140574359,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140574359,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs560924811","clinical_significance":[],"start":140574361,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140574361,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs991472671","end":140574363,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140574363,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1798216465","clinical_significance":[],"start":140574364,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140574364,"strand":1,"feature_type":"variation"},{"id":"rs920824630","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574366,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140574366},{"seq_region_name":"7","id":"rs1208686364","clinical_significance":[],"alleles":["C","T"],"end":140574367,"strand":1,"feature_type":"variation","start":140574367,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140574369,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140574369,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798216781","clinical_significance":[]},{"source":"dbSNP","start":140574369,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140574370,"alleles":["CT","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs2130613354","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1447489691","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574371,"feature_type":"variation","strand":1,"end":140574371,"alleles":["G","A"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574373,"source":"dbSNP","strand":1,"feature_type":"variation","end":140574373,"alleles":["C","G"],"seq_region_name":"7","id":"rs930317454","clinical_significance":[]},{"start":140574375,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140574375,"strand":1,"feature_type":"variation","id":"rs983058105","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574376,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140574376,"clinical_significance":[],"id":"rs1425608169","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1798217317","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574377,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140574377},{"end":140574378,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140574378,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1475771833"},{"seq_region_name":"7","id":"rs1190644755","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574382,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140574382},{"end":140574385,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140574385,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1798217643","seq_region_name":"7","clinical_significance":[]},{"start":140574387,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140574387,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs898039401","clinical_significance":[]},{"seq_region_name":"7","id":"rs1388547795","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574391,"source":"dbSNP","strand":1,"feature_type":"variation","end":140574391,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs994248188","alleles":["G","A","C","T"],"end":140574392,"feature_type":"variation","strand":1,"source":"dbSNP","start":140574392,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1798218595","clinical_significance":[],"start":140574394,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140574394,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"alleles":["T","A","C"],"end":140574401,"feature_type":"variation","strand":1,"source":"dbSNP","start":140574401,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs149200971","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs540506955","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140574407,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574407},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574410,"feature_type":"variation","strand":1,"end":140574410,"alleles":["G","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs375314055"},{"source":"dbSNP","start":140574412,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140574412,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1018154679"},{"end":140574416,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","start":140574416,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs142412842","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs900323930","alleles":["C","A","T"],"end":140574417,"feature_type":"variation","strand":1,"source":"dbSNP","start":140574417,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574418,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140574418,"seq_region_name":"7","id":"rs1345762615","clinical_significance":[]},{"start":140574419,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140574419,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798219471","clinical_significance":[]},{"start":140574428,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140574428,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1436602555","clinical_significance":[]},{"alleles":["C","T"],"end":140574431,"feature_type":"variation","strand":1,"source":"dbSNP","start":140574431,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798219699"},{"alleles":["G","A"],"end":140574433,"strand":1,"feature_type":"variation","start":140574433,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585667722","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs989942648","source":"dbSNP","start":140574438,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140574438,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs764508302","feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140574439,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574439},{"alleles":["A","C"],"end":140574441,"feature_type":"variation","strand":1,"source":"dbSNP","start":140574441,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798220198"},{"clinical_significance":[],"id":"rs931798329","seq_region_name":"7","source":"dbSNP","start":140574442,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140574442,"alleles":["C","A"],"feature_type":"variation","strand":1},{"end":140574443,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140574443,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1163645680","seq_region_name":"7","clinical_significance":[]},{"id":"rs1563151977","seq_region_name":"7","clinical_significance":[],"end":140574444,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140574444,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["T","A","G"],"end":140574446,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574446,"source":"dbSNP","id":"rs914480876","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574447,"feature_type":"variation","strand":1,"end":140574447,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1798220775"},{"source":"dbSNP","start":140574449,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140574449,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs967290661"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574450,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140574450,"seq_region_name":"7","id":"rs1798221034","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798221131","alleles":["G","A"],"end":140574454,"feature_type":"variation","strand":1,"source":"dbSNP","start":140574454,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs879731773","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574458,"source":"dbSNP","strand":1,"feature_type":"variation","end":140574458,"alleles":["A","G"]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140574459,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574459,"clinical_significance":[],"seq_region_name":"7","id":"rs1585667799"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563151995","feature_type":"variation","strand":1,"end":140574460,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574460},{"alleles":["C","T"],"end":140574461,"feature_type":"variation","strand":1,"source":"dbSNP","start":140574461,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs113475472"},{"alleles":["G","A","C"],"end":140574462,"feature_type":"variation","strand":1,"source":"dbSNP","start":140574462,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1369651834"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574467,"feature_type":"variation","strand":1,"end":140574467,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1010924295"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585667834","source":"dbSNP","start":140574471,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140574471,"alleles":["A","T"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140574475,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574475,"source":"dbSNP","seq_region_name":"7","id":"rs1798222080","clinical_significance":[]},{"id":"rs1020954423","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574479,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140574479},{"id":"rs1798222304","seq_region_name":"7","clinical_significance":[],"start":140574481,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140574481,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1437788159","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574482,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140574482},{"alleles":["G","A"],"end":140574484,"strand":1,"feature_type":"variation","start":140574484,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs562869428","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs183712412","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574487,"feature_type":"variation","strand":1,"end":140574487,"alleles":["A","G"]},{"strand":1,"feature_type":"variation","end":140574490,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574490,"source":"dbSNP","seq_region_name":"7","id":"rs1798222773","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798222895","end":140574500,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140574500,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs548306967","clinical_significance":[],"end":140574501,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140574501,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs916121920","alleles":["A","G"],"end":140574502,"feature_type":"variation","strand":1,"source":"dbSNP","start":140574502,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574503,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140574503,"clinical_significance":[],"seq_region_name":"7","id":"rs1035230442"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1232141793","alleles":["C","T"],"end":140574507,"feature_type":"variation","strand":1,"source":"dbSNP","start":140574507,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140574508,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574508,"clinical_significance":[],"seq_region_name":"7","id":"rs1350611155"},{"seq_region_name":"7","id":"rs1639944","clinical_significance":[],"start":140574509,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140574509,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1335129163","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574510,"feature_type":"variation","strand":1,"end":140574510,"alleles":["C","T"]},{"id":"rs759859659","seq_region_name":"7","clinical_significance":[],"start":140574513,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140574513,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574517,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CCC","CCCC"],"end":140574519,"seq_region_name":"7","id":"rs1323889794","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1388361380","source":"dbSNP","start":140574519,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140574519,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140574520,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574520,"source":"dbSNP","seq_region_name":"7","id":"rs1448147660","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585668011","clinical_significance":[],"start":140574522,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140574522,"alleles":["T","G"],"strand":1,"feature_type":"variation"},{"end":140574532,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140574532,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798224866"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574533,"feature_type":"variation","strand":1,"end":140574533,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1798224966"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574535,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140574535,"clinical_significance":[],"seq_region_name":"7","id":"rs1798225059"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574536,"feature_type":"variation","strand":1,"end":140574536,"alleles":["C","T"],"clinical_significance":[],"id":"rs1798225166","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1210657461","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574537,"source":"dbSNP","strand":1,"feature_type":"variation","end":140574537,"alleles":["A","C","G"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574540,"source":"dbSNP","strand":1,"feature_type":"variation","end":140574540,"alleles":["T","C"],"seq_region_name":"7","id":"rs990966203","clinical_significance":[]},{"clinical_significance":[],"id":"rs898086220","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574542,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140574542},{"clinical_significance":[],"seq_region_name":"7","id":"rs993741229","source":"dbSNP","start":140574543,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140574543,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574544,"source":"dbSNP","strand":1,"feature_type":"variation","end":140574544,"alleles":["A","G"],"seq_region_name":"7","id":"rs1798225743","clinical_significance":[]},{"alleles":["G","T"],"end":140574545,"strand":1,"feature_type":"variation","start":140574545,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1047192799","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585668060","feature_type":"variation","strand":1,"end":140574549,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574549},{"strand":1,"feature_type":"variation","end":140574549,"alleles":["A","AA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574549,"source":"dbSNP","seq_region_name":"7","id":"rs1798226076","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574550,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140574550,"clinical_significance":[],"seq_region_name":"7","id":"rs1798226176"},{"end":140574552,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140574552,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798226286","clinical_significance":[]},{"source":"dbSNP","start":140574557,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140574557,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs187436329"},{"end":140574562,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140574562,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1798226503","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140574567,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140574567,"alleles":["A","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1464559381"},{"clinical_significance":[],"seq_region_name":"7","id":"rs374408390","source":"dbSNP","start":140574568,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140574568,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs545049729","clinical_significance":[],"end":140574569,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140574569,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1450309572","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574573,"feature_type":"variation","strand":1,"end":140574573,"alleles":["C","T"]},{"source":"dbSNP","start":140574580,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140574580,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1379102295"},{"start":140574588,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140574588,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130613960","clinical_significance":[]},{"source":"dbSNP","start":140574599,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140574599,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798227220"},{"source":"dbSNP","start":140574603,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140574603,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798227323"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574604,"source":"dbSNP","strand":1,"feature_type":"variation","end":140574604,"alleles":["T","C"],"id":"rs1798227434","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574608,"source":"dbSNP","strand":1,"feature_type":"variation","end":140574608,"alleles":["C","CC"],"id":"rs1250715614","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574609,"feature_type":"variation","strand":1,"end":140574617,"alleles":["TAGGGGTTA","-"],"clinical_significance":[],"seq_region_name":"7","id":"rs1798227775"},{"seq_region_name":"7","id":"rs1212734709","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574610,"source":"dbSNP","strand":1,"feature_type":"variation","end":140574619,"alleles":["AGGGGTTACA","A"]},{"alleles":["G","A","C"],"end":140574611,"strand":1,"feature_type":"variation","start":140574611,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1476905023","clinical_significance":[]},{"start":140574614,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C","T"],"end":140574614,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs570803360","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140574617,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574617,"source":"dbSNP","seq_region_name":"7","id":"rs538099204","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140574618,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574618,"source":"dbSNP","seq_region_name":"7","id":"rs1458805627","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798228946","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574619,"source":"dbSNP","strand":1,"feature_type":"variation","end":140574618,"alleles":["-","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1018038221","feature_type":"variation","strand":1,"alleles":["G","C","T"],"end":140574622,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574622},{"alleles":["C","T"],"end":140574623,"strand":1,"feature_type":"variation","start":140574623,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs907543433","clinical_significance":[]},{"seq_region_name":"7","id":"rs944492211","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574626,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140574626},{"seq_region_name":"7","id":"rs556319811","clinical_significance":[],"start":140574633,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140574633,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1438310928","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140574640,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574640,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140574643,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574643,"clinical_significance":[],"id":"rs1368579072","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1011426677","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574644,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140574644},{"end":140574645,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140574645,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1798230102","seq_region_name":"7","clinical_significance":[]},{"start":140574647,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140574647,"alleles":["G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798230196","clinical_significance":[]},{"clinical_significance":[],"id":"rs1436041965","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574648,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140574648},{"clinical_significance":[],"id":"rs550512041","seq_region_name":"7","end":140574649,"alleles":["A","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140574649,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1798230576","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140574651,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574651,"source":"dbSNP"},{"alleles":["C","T"],"end":140574656,"strand":1,"feature_type":"variation","start":140574656,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1021433089","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140574657,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574657,"source":"dbSNP","seq_region_name":"7","id":"rs1325090475","clinical_significance":[]},{"start":140574658,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C"],"end":140574658,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798230920","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs921661428","end":140574660,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140574660,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1329037977","clinical_significance":[],"alleles":["C","A","T"],"end":140574663,"strand":1,"feature_type":"variation","start":140574663,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574663,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CC","C"],"end":140574664,"seq_region_name":"7","id":"rs1798231282","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798231390","feature_type":"variation","strand":1,"alleles":["T","A"],"end":140574665,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574665},{"id":"rs1426476765","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574671,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140574671},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798231588","alleles":["C","A"],"end":140574672,"feature_type":"variation","strand":1,"source":"dbSNP","start":140574672,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1798231675","clinical_significance":[],"start":140574673,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140574673,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1174866141","clinical_significance":[],"alleles":["G","A"],"end":140574675,"strand":1,"feature_type":"variation","start":140574675,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140574677,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140574677,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1477229705","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1798232106","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140574678,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574678,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798232217","alleles":["T","G"],"end":140574682,"feature_type":"variation","strand":1,"source":"dbSNP","start":140574682,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140574684,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574684,"source":"dbSNP","id":"rs977350154","seq_region_name":"7","clinical_significance":[]},{"alleles":["TTT","TT"],"end":140574686,"feature_type":"variation","strand":1,"source":"dbSNP","start":140574684,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs967720362"},{"source":"dbSNP","start":140574690,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140574690,"alleles":["T","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798232543"},{"start":140574694,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140574694,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1330355064","clinical_significance":[]},{"seq_region_name":"7","id":"rs931826237","clinical_significance":[],"start":140574695,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140574695,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798232884","source":"dbSNP","start":140574698,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140574698,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140574699,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574699,"source":"dbSNP","seq_region_name":"7","id":"rs1249518504","clinical_significance":[]},{"seq_region_name":"7","id":"rs79635777","clinical_significance":[],"start":140574703,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140574703,"alleles":["C","A","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs752826001","clinical_significance":[],"strand":1,"feature_type":"variation","end":140574705,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574705,"source":"dbSNP"},{"alleles":["A","T"],"end":140574706,"feature_type":"variation","strand":1,"source":"dbSNP","start":140574706,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs991410932"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130614346","source":"dbSNP","start":140574716,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140574716,"alleles":["C","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130614353","end":140574717,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140574717,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140574719,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140574719,"alleles":["G","A","C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs74300710"},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140574720,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574720,"clinical_significance":[],"seq_region_name":"7","id":"rs1228888283"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1210561167","feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140574727,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574727},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130614388","source":"dbSNP","start":140574728,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140574728,"alleles":["A","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1798234210","seq_region_name":"7","feature_type":"variation","strand":1,"end":140574730,"alleles":["G","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574730},{"seq_region_name":"7","id":"rs1269696625","clinical_significance":[],"start":140574732,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140574732,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574733,"feature_type":"variation","strand":1,"end":140574733,"alleles":["A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130614420"},{"source":"dbSNP","start":140574735,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140574735,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130614428"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574737,"feature_type":"variation","strand":1,"end":140574737,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1798234553"},{"seq_region_name":"7","id":"rs1563152165","clinical_significance":[],"end":140574738,"alleles":["G","C","T"],"strand":1,"feature_type":"variation","start":140574738,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140574746,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140574746,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1268706731","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130614461","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574747,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140574747},{"clinical_significance":[],"id":"rs1798235057","seq_region_name":"7","alleles":["T","A","G"],"end":140574748,"feature_type":"variation","strand":1,"source":"dbSNP","start":140574748,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs2130614477","seq_region_name":"7","clinical_significance":[],"alleles":["T","G"],"end":140574750,"strand":1,"feature_type":"variation","start":140574750,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140574754,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140574754,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798235236"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574756,"feature_type":"variation","strand":1,"end":140574756,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130614494"},{"end":140574757,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140574757,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130614506","clinical_significance":[]},{"clinical_significance":[],"id":"rs942091505","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","C","T"],"end":140574759,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574759},{"alleles":["C","T"],"end":140574762,"feature_type":"variation","strand":1,"source":"dbSNP","start":140574762,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1359864240"},{"seq_region_name":"7","id":"rs1798235597","clinical_significance":[],"start":140574764,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140574764,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"start":140574765,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140574765,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs2130614534","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130614541","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574767,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140574767},{"id":"rs945928450","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140574772,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574772,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1798235910","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574778,"source":"dbSNP","strand":1,"feature_type":"variation","end":140574778,"alleles":["T","C"]},{"start":140574780,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140574780,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798236078","clinical_significance":[]},{"clinical_significance":[],"id":"rs1450153267","seq_region_name":"7","source":"dbSNP","start":140574790,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140574790,"alleles":["G","A"],"feature_type":"variation","strand":1},{"id":"rs2130614573","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140574795,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574795,"source":"dbSNP"},{"end":140574804,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140574804,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1336268837"},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140574809,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574809,"source":"dbSNP","seq_region_name":"7","id":"rs1042452946","clinical_significance":[]},{"seq_region_name":"7","id":"rs973998949","clinical_significance":[],"strand":1,"feature_type":"variation","end":140574812,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574812,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1233253087","end":140574814,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140574814,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574821,"feature_type":"variation","strand":1,"end":140574821,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1169555100"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574833,"feature_type":"variation","strand":1,"end":140574833,"alleles":["C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1307650604"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574834,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140574834,"clinical_significance":[],"seq_region_name":"7","id":"rs554291651"},{"feature_type":"variation","strand":1,"end":140574842,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574842,"clinical_significance":[],"seq_region_name":"7","id":"rs2130614621"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798237223","source":"dbSNP","start":140574846,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140574846,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1156890761","clinical_significance":[],"alleles":["G","A"],"end":140574847,"strand":1,"feature_type":"variation","start":140574847,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1798237454","clinical_significance":[],"start":140574848,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140574848,"alleles":["T","G"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140574849,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140574849,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1184457874","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798237677","feature_type":"variation","strand":1,"end":140574854,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574854},{"alleles":["A","C"],"end":140574862,"strand":1,"feature_type":"variation","start":140574862,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1474891126","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140574863,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574863,"clinical_significance":[],"id":"rs1585668625","seq_region_name":"7"},{"end":140574870,"alleles":["AAAAAAA","AAAAAAAA"],"strand":1,"feature_type":"variation","start":140574864,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1237515881","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574866,"feature_type":"variation","strand":1,"end":140574866,"alleles":["A","C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1411219532"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1211626282","end":140574868,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140574868,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140574869,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140574869,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1461482303","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140574871,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574871,"clinical_significance":[],"seq_region_name":"7","id":"rs1585668666"},{"seq_region_name":"7","id":"rs902508635","clinical_significance":[],"strand":1,"feature_type":"variation","end":140574872,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574872,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140574878,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574878,"clinical_significance":[],"seq_region_name":"7","id":"rs1798238612"},{"feature_type":"variation","strand":1,"end":140574880,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574880,"clinical_significance":[],"seq_region_name":"7","id":"rs1164565546"},{"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140574881,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574881,"clinical_significance":[],"id":"rs572751844","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585668718","source":"dbSNP","start":140574882,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140574882,"feature_type":"variation","strand":1},{"start":140574888,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140574888,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1344088913","clinical_significance":[]},{"clinical_significance":[],"id":"rs540543718","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574889,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140574889},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585668751","source":"dbSNP","start":140574892,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140574892,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140574893,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574893,"clinical_significance":[],"seq_region_name":"7","id":"rs1798239422"},{"source":"dbSNP","start":140574894,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140574894,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1385889614"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798239670","end":140574895,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140574895,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140574896,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574896,"clinical_significance":[],"seq_region_name":"7","id":"rs1380205088"},{"seq_region_name":"7","id":"rs895210538","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574897,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140574897},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140574900,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574900,"source":"dbSNP","id":"rs1585668797","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798240090","clinical_significance":[],"start":140574902,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140574902,"strand":1,"feature_type":"variation"},{"alleles":["C","T"],"end":140574903,"feature_type":"variation","strand":1,"source":"dbSNP","start":140574903,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs190762006"},{"strand":1,"feature_type":"variation","end":140574912,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574912,"source":"dbSNP","id":"rs1027758774","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs372326667","clinical_significance":[],"start":140574913,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140574913,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1309214447","seq_region_name":"7","source":"dbSNP","start":140574914,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140574914,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1431991989","source":"dbSNP","start":140574916,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140574916,"alleles":["A","G"],"feature_type":"variation","strand":1},{"alleles":["G","A","T"],"end":140574918,"feature_type":"variation","strand":1,"source":"dbSNP","start":140574918,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1798240739","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140574919,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574919,"source":"dbSNP","seq_region_name":"7","id":"rs182441885","clinical_significance":[]},{"id":"rs577187283","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574934,"source":"dbSNP","strand":1,"feature_type":"variation","end":140574934,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs890662739","source":"dbSNP","start":140574935,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140574935,"alleles":["G","A","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1189435431","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140574936,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574936},{"clinical_significance":[],"id":"rs1350457176","seq_region_name":"7","alleles":["C","T"],"end":140574942,"feature_type":"variation","strand":1,"source":"dbSNP","start":140574942,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140574943,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574943,"source":"dbSNP","id":"rs943692549","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1256676203","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574945,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140574945},{"clinical_significance":[],"seq_region_name":"7","id":"rs1015094367","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574949,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140574949},{"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140574951,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574951,"source":"dbSNP","seq_region_name":"7","id":"rs966102094","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs544452480","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140574952,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574952},{"clinical_significance":[],"seq_region_name":"7","id":"rs1209468653","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574956,"feature_type":"variation","strand":1,"end":140574956,"alleles":["G","A"]},{"id":"rs1798242672","seq_region_name":"7","clinical_significance":[],"end":140574958,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140574958,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574960,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140574960,"seq_region_name":"7","id":"rs1798242805","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130614949","feature_type":"variation","strand":1,"end":140574964,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574964},{"end":140574966,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140574966,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798242921"},{"alleles":["T","C"],"end":140574968,"strand":1,"feature_type":"variation","start":140574968,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs899600215","clinical_significance":[]},{"id":"rs1798243112","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140574972,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574972,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1860840","clinical_significance":[],"strand":1,"feature_type":"variation","end":140574976,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574976,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140574977,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574977,"clinical_significance":[],"seq_region_name":"7","id":"rs1798243455"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574980,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140574980,"clinical_significance":[],"seq_region_name":"7","id":"rs1798243596"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140574981,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140574981,"clinical_significance":[],"id":"rs140721541","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140574982,"alleles":["T","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140574982,"source":"dbSNP","seq_region_name":"7","id":"rs1179801815","clinical_significance":[]},{"source":"dbSNP","start":140574983,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140574983,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1798244163","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1250986926","alleles":["C","A","T"],"end":140574986,"feature_type":"variation","strand":1,"source":"dbSNP","start":140574986,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","T"],"end":140574989,"feature_type":"variation","strand":1,"source":"dbSNP","start":140574989,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs527434761"},{"start":140574997,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140574997,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs903006616","clinical_significance":[]},{"alleles":["A","T"],"end":140575000,"strand":1,"feature_type":"variation","start":140575000,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585669108","clinical_significance":[]},{"seq_region_name":"7","id":"rs1248449610","clinical_significance":[],"start":140575001,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140575001,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1798245207","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140575002,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575002,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1798245375","clinical_significance":[],"start":140575003,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140575003,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1798245539","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140575006,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575006,"source":"dbSNP"},{"id":"rs866819714","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575015,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140575015},{"seq_region_name":"7","id":"rs1798245857","clinical_significance":[],"start":140575022,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140575022,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140575027,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575027,"clinical_significance":[],"id":"rs1798245954","seq_region_name":"7"},{"seq_region_name":"7","id":"rs750165447","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140575029,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575029,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140575035,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575035,"source":"dbSNP","seq_region_name":"7","id":"rs1798246167","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1412178482","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140575039,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575039},{"seq_region_name":"7","id":"rs1798246412","clinical_significance":[],"start":140575040,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140575040,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140575044,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575044,"source":"dbSNP","seq_region_name":"7","id":"rs1188955343","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798246612","clinical_significance":[],"strand":1,"feature_type":"variation","end":140575045,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575045,"source":"dbSNP"},{"seq_region_name":"7","id":"rs999219494","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575051,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140575051},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140575055,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575055,"clinical_significance":[],"seq_region_name":"7","id":"rs1297908708"},{"strand":1,"feature_type":"variation","end":140575056,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575056,"source":"dbSNP","seq_region_name":"7","id":"rs2130615182","clinical_significance":[]},{"seq_region_name":"7","id":"rs10273005","clinical_significance":[],"start":140575058,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140575058,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575064,"feature_type":"variation","strand":1,"alleles":["AAAAAAA","AAAAAAAA"],"end":140575070,"clinical_significance":[],"seq_region_name":"7","id":"rs1457062359"},{"start":140575071,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140575071,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1168159409","clinical_significance":[]},{"seq_region_name":"7","id":"rs527718170","clinical_significance":[],"end":140575078,"alleles":["C","A","G","T"],"strand":1,"feature_type":"variation","start":140575078,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140575079,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140575079,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs552153301","clinical_significance":[]},{"seq_region_name":"7","id":"rs1416460468","clinical_significance":[],"end":140575081,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140575081,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1431980209","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575086,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140575086},{"end":140575087,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140575087,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs928499067"},{"start":140575096,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140575096,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs779748350","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575099,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140575099,"seq_region_name":"7","id":"rs1798248338","clinical_significance":[]},{"clinical_significance":[],"id":"rs750967578","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575104,"feature_type":"variation","strand":1,"end":140575109,"alleles":["AACTCA","AACTCAACTCA"]},{"seq_region_name":"7","id":"rs1798248661","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575106,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140575106},{"seq_region_name":"7","id":"rs1056442864","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140575115,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575115,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575116,"feature_type":"variation","strand":1,"end":140575116,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1860841"},{"seq_region_name":"7","id":"rs1012328193","clinical_significance":[],"start":140575121,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140575121,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs561098097","feature_type":"variation","strand":1,"end":140575123,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575123},{"clinical_significance":[],"seq_region_name":"7","id":"rs1314854400","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575124,"feature_type":"variation","strand":1,"end":140575124,"alleles":["G","A"]},{"start":140575129,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140575129,"alleles":["A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798249626","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798249795","feature_type":"variation","strand":1,"end":140575137,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575137},{"alleles":["AAAAA","AAAA"],"end":140575144,"feature_type":"variation","strand":1,"source":"dbSNP","start":140575140,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1338803545","seq_region_name":"7"},{"start":140575141,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140575141,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1244223594","clinical_significance":[]},{"alleles":["G","A"],"end":140575145,"strand":1,"feature_type":"variation","start":140575145,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1798250328","seq_region_name":"7","clinical_significance":[]},{"end":140575147,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140575147,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798250452"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1298571119","end":140575148,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140575148,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130615393","source":"dbSNP","start":140575151,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140575151,"alleles":["T","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798250665","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575157,"feature_type":"variation","strand":1,"end":140575166,"alleles":["AAAAGAAAAG","AAAAG"]},{"source":"dbSNP","start":140575160,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140575160,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs887953609"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575161,"source":"dbSNP","strand":1,"feature_type":"variation","end":140575161,"alleles":["G","A","T"],"seq_region_name":"7","id":"rs1202746984","clinical_significance":[]},{"seq_region_name":"7","id":"rs1230323202","clinical_significance":[],"end":140575167,"alleles":["C","-"],"strand":1,"feature_type":"variation","start":140575167,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs963453723","seq_region_name":"7","clinical_significance":[],"start":140575168,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140575168,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798251256","end":140575173,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140575173,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1798251377","seq_region_name":"7","feature_type":"variation","strand":1,"end":140575174,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575174},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575177,"feature_type":"variation","strand":1,"alleles":["AA","A"],"end":140575178,"clinical_significance":[],"seq_region_name":"7","id":"rs1307000367"},{"alleles":["T","C"],"end":140575179,"strand":1,"feature_type":"variation","start":140575179,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1004966886","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575193,"feature_type":"variation","strand":1,"end":140575193,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs780615700"},{"clinical_significance":[],"seq_region_name":"7","id":"rs973500568","end":140575198,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140575198,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140575202,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140575202,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1585669445","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs919457937","feature_type":"variation","strand":1,"end":140575203,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575203},{"seq_region_name":"7","id":"rs1393280398","clinical_significance":[],"start":140575212,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140575212,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1798252266","clinical_significance":[],"alleles":["A","C"],"end":140575215,"strand":1,"feature_type":"variation","start":140575215,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140575218,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140575218,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs747724609"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1320571084","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575226,"feature_type":"variation","strand":1,"end":140575226,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs1454946624","clinical_significance":[],"start":140575230,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140575230,"alleles":["T","G"],"strand":1,"feature_type":"variation"},{"end":140575231,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140575231,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1361989076","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798252843","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575234,"feature_type":"variation","strand":1,"end":140575234,"alleles":["T","C"]},{"alleles":["G","C"],"end":140575236,"strand":1,"feature_type":"variation","start":140575236,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1158359501","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798253162","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575244,"feature_type":"variation","strand":1,"end":140575244,"alleles":["C","T"]},{"clinical_significance":[],"id":"rs770274009","seq_region_name":"7","end":140575245,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140575245,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140575247,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140575247,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798253541"},{"start":140575248,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140575248,"strand":1,"feature_type":"variation","id":"rs929493452","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140575250,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575250,"source":"dbSNP","seq_region_name":"7","id":"rs1798253893","clinical_significance":[]},{"clinical_significance":[],"id":"rs1798254018","seq_region_name":"7","source":"dbSNP","start":140575256,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140575256,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs966291089","source":"dbSNP","start":140575259,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140575259,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575262,"feature_type":"variation","strand":1,"end":140575262,"alleles":["T","A"],"clinical_significance":[],"id":"rs1191521933","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1253401573","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140575266,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575266},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798254498","feature_type":"variation","strand":1,"end":140575270,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575270},{"clinical_significance":[],"seq_region_name":"7","id":"rs1248945701","feature_type":"variation","strand":1,"end":140575276,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575276},{"alleles":["G","T"],"end":140575277,"strand":1,"feature_type":"variation","start":140575277,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs117550186","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140575278,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575278,"source":"dbSNP","id":"rs1028639620","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs767194575","feature_type":"variation","strand":1,"end":140575289,"alleles":["TTTTTTT","TTTTTT","TTTTTTTT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575283},{"strand":1,"feature_type":"variation","end":140575290,"alleles":["G","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575290,"source":"dbSNP","id":"rs1798255107","seq_region_name":"7","clinical_significance":[]},{"start":140575293,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140575293,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs953290166","clinical_significance":[]},{"source":"dbSNP","start":140575298,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140575298,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798255303"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1391625423","feature_type":"variation","strand":1,"alleles":["T","TTTTTTTTTT"],"end":140575299,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575299},{"source":"dbSNP","start":140575301,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140575301,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1447342857"},{"feature_type":"variation","strand":1,"end":140575302,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575302,"clinical_significance":[],"seq_region_name":"7","id":"rs1798255637"},{"start":140575312,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140575312,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1350717032","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798255839","clinical_significance":[],"end":140575315,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140575315,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs943576421","source":"dbSNP","start":140575318,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140575318,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["TG","-"],"end":140575326,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575325,"source":"dbSNP","seq_region_name":"7","id":"rs1798256087","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575326,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140575326,"seq_region_name":"7","id":"rs989892061","clinical_significance":[]},{"alleles":["T","G"],"end":140575328,"feature_type":"variation","strand":1,"source":"dbSNP","start":140575328,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1234034967"},{"id":"rs1798256399","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575330,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140575330},{"seq_region_name":"7","id":"rs187094215","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140575333,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575333,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1798256638","seq_region_name":"7","source":"dbSNP","start":140575338,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140575338,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1369769119","alleles":["G","A"],"end":140575341,"feature_type":"variation","strand":1,"source":"dbSNP","start":140575341,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs114556339","source":"dbSNP","start":140575348,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140575348,"alleles":["C","T"],"feature_type":"variation","strand":1},{"id":"rs899485138","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575354,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140575354},{"id":"rs1382080569","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140575357,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575357,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575358,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140575358,"seq_region_name":"7","id":"rs1563152545","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575359,"feature_type":"variation","strand":1,"end":140575359,"alleles":["T","G"],"clinical_significance":[],"id":"rs1563152547","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1466965940","clinical_significance":[],"start":140575362,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140575362,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798257600","source":"dbSNP","start":140575368,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["GGG","GG"],"end":140575370,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1798257724","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575371,"feature_type":"variation","strand":1,"end":140575371,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs947152457","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575377,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140575377},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798257934","source":"dbSNP","start":140575379,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140575379,"alleles":["A","G"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140575380,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575380,"source":"dbSNP","seq_region_name":"7","id":"rs1400746935","clinical_significance":[]},{"seq_region_name":"7","id":"rs1395524055","clinical_significance":[],"start":140575382,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","AA"],"end":140575382,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798258304","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575386,"feature_type":"variation","strand":1,"end":140575386,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs967207888","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140575393,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575393,"source":"dbSNP"},{"id":"rs1563152563","seq_region_name":"7","clinical_significance":[],"end":140575398,"alleles":["C","-"],"strand":1,"feature_type":"variation","start":140575398,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs977230957","seq_region_name":"7","feature_type":"variation","strand":1,"end":140575401,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575401},{"strand":1,"feature_type":"variation","end":140575402,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575402,"source":"dbSNP","id":"rs902894355","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs138550798","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575406,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140575406},{"clinical_significance":[],"id":"rs1798259145","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575407,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140575407},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140575408,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575408,"source":"dbSNP","seq_region_name":"7","id":"rs1426981166","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575413,"feature_type":"variation","strand":1,"end":140575413,"alleles":["T","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1035905790"},{"clinical_significance":[],"seq_region_name":"7","id":"rs938601833","end":140575414,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140575414,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1798259557","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575416,"feature_type":"variation","strand":1,"end":140575416,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1201109967","source":"dbSNP","start":140575419,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140575419,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798259757","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140575421,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575421},{"clinical_significance":[],"seq_region_name":"7","id":"rs1226470734","feature_type":"variation","strand":1,"end":140575427,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575427},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575431,"feature_type":"variation","strand":1,"alleles":["TTATGATGCATATAGCTT","TT"],"end":140575448,"clinical_significance":[],"seq_region_name":"7","id":"rs1278883804"},{"clinical_significance":[],"id":"rs1798260072","seq_region_name":"7","source":"dbSNP","start":140575442,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140575442,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs568907191","alleles":["C","G","T"],"end":140575453,"feature_type":"variation","strand":1,"source":"dbSNP","start":140575453,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140575456,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575456,"clinical_significance":[],"seq_region_name":"7","id":"rs190346815"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575457,"source":"dbSNP","strand":1,"feature_type":"variation","end":140575457,"alleles":["G","A"],"id":"rs948012382","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1049144288","seq_region_name":"7","source":"dbSNP","start":140575464,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140575464,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1798260652","seq_region_name":"7","source":"dbSNP","start":140575465,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140575465,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs887835848","seq_region_name":"7","source":"dbSNP","start":140575469,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140575469,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1312580625","source":"dbSNP","start":140575480,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140575480,"feature_type":"variation","strand":1},{"start":140575481,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140575481,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1005027781","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575484,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140575484,"clinical_significance":[],"seq_region_name":"7","id":"rs1798261079"},{"alleles":["A","G"],"end":140575488,"strand":1,"feature_type":"variation","start":140575488,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1012767581","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140575491,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575491,"clinical_significance":[],"id":"rs771276515","seq_region_name":"7"},{"start":140575497,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140575497,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","id":"rs1036471028","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140575499,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575499,"clinical_significance":[],"seq_region_name":"7","id":"rs1311040196"},{"strand":1,"feature_type":"variation","end":140575506,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575506,"source":"dbSNP","seq_region_name":"7","id":"rs1798261709","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575506,"feature_type":"variation","strand":1,"alleles":["AA","A"],"end":140575507,"clinical_significance":[],"id":"rs1433847933","seq_region_name":"7"},{"id":"rs147203642","seq_region_name":"7","clinical_significance":[],"start":140575513,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TTTTTT","TTTTTTT"],"end":140575518,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1482923203","end":140575519,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140575519,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs902122681","clinical_significance":[],"start":140575522,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140575522,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs997770669","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140575526,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575526},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140575528,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575528,"clinical_significance":[],"seq_region_name":"7","id":"rs1460594972"},{"id":"rs1372731874","seq_region_name":"7","clinical_significance":[],"alleles":["ATAT","AT"],"end":140575532,"strand":1,"feature_type":"variation","start":140575529,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs779687385","source":"dbSNP","start":140575530,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140575530,"alleles":["T","C"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140575532,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575532,"clinical_significance":[],"seq_region_name":"7","id":"rs950832666"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575533,"source":"dbSNP","strand":1,"feature_type":"variation","end":140575533,"alleles":["T","C"],"seq_region_name":"7","id":"rs987674994","clinical_significance":[]},{"seq_region_name":"7","id":"rs912044226","clinical_significance":[],"start":140575534,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140575534,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140575537,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140575537,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798263140"},{"seq_region_name":"7","id":"rs953075261","clinical_significance":[],"end":140575541,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140575541,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575542,"source":"dbSNP","strand":1,"feature_type":"variation","end":140575542,"alleles":["G","C"],"id":"rs1253017926","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140575543,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575543,"source":"dbSNP","seq_region_name":"7","id":"rs1798263454","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798263579","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575552,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140575552},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798263695","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575556,"feature_type":"variation","strand":1,"end":140575556,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585670086","source":"dbSNP","start":140575567,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140575567,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs140276450","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575573,"source":"dbSNP","strand":1,"feature_type":"variation","end":140575573,"alleles":["A","G"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575574,"feature_type":"variation","strand":1,"end":140575574,"alleles":["C","T"],"clinical_significance":[],"id":"rs1798264043","seq_region_name":"7"},{"seq_region_name":"7","id":"rs920969285","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140575583,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575583,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575587,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140575587,"clinical_significance":[],"seq_region_name":"7","id":"rs947077787"},{"id":"rs1233334128","seq_region_name":"7","clinical_significance":[],"end":140575595,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140575595,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575597,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140575597,"seq_region_name":"7","id":"rs1798264494","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575600,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140575600,"seq_region_name":"7","id":"rs1798264612","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140575601,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575601,"clinical_significance":[],"seq_region_name":"7","id":"rs1043083178"},{"seq_region_name":"7","id":"rs1290933463","clinical_significance":[],"strand":1,"feature_type":"variation","end":140575602,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575602,"source":"dbSNP"},{"source":"dbSNP","start":140575604,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140575604,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1414044201"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575606,"source":"dbSNP","strand":1,"feature_type":"variation","end":140575606,"alleles":["A","G"],"seq_region_name":"7","id":"rs1336279405","clinical_significance":[]},{"seq_region_name":"7","id":"rs1563152717","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140575607,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575607,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1330568756","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575609,"feature_type":"variation","strand":1,"end":140575609,"alleles":["G","C"]},{"alleles":["G","A"],"end":140575611,"feature_type":"variation","strand":1,"source":"dbSNP","start":140575611,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798265320"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798265437","alleles":["G","C"],"end":140575612,"feature_type":"variation","strand":1,"source":"dbSNP","start":140575612,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140575613,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140575613,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1011211964"},{"seq_region_name":"7","id":"rs1798265669","clinical_significance":[],"start":140575616,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140575616,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575619,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140575619,"clinical_significance":[],"seq_region_name":"7","id":"rs1585670209"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798265890","source":"dbSNP","start":140575629,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140575629,"feature_type":"variation","strand":1},{"alleles":["T","A","C"],"end":140575631,"feature_type":"variation","strand":1,"source":"dbSNP","start":140575631,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1021396449"},{"end":140575632,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140575632,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs543719503","seq_region_name":"7","clinical_significance":[]},{"end":140575636,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140575636,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1396031980"},{"seq_region_name":"7","id":"rs934384325","clinical_significance":[],"strand":1,"feature_type":"variation","end":140575638,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575638,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1798266372","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140575644,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575644,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1178781334","alleles":["A","G"],"end":140575645,"feature_type":"variation","strand":1,"source":"dbSNP","start":140575645,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1463058341","source":"dbSNP","start":140575646,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140575646,"alleles":["G","A"],"feature_type":"variation","strand":1},{"end":140575651,"alleles":["GGAA","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140575648,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798266707"},{"seq_region_name":"7","id":"rs1415717664","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["GGAATACCATG","-"],"end":140575658,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575648,"source":"dbSNP"},{"id":"rs1765681595","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575650,"source":"dbSNP","strand":1,"feature_type":"variation","end":140575650,"alleles":["A","G","T"]},{"source":"dbSNP","start":140575652,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140575652,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1164310834"},{"end":140575656,"alleles":["ACCA","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140575653,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798266991"},{"clinical_significance":[],"seq_region_name":"7","id":"rs967094694","source":"dbSNP","start":140575657,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140575657,"alleles":["T","C"],"feature_type":"variation","strand":1},{"end":140575661,"alleles":["GCAA","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140575658,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798267207"},{"end":140575659,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140575659,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1235160235","clinical_significance":[]},{"alleles":["A","T"],"end":140575661,"feature_type":"variation","strand":1,"source":"dbSNP","start":140575661,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1180104987"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575665,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140575665,"seq_region_name":"7","id":"rs1437658318","clinical_significance":[]},{"seq_region_name":"7","id":"rs577224246","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140575668,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575668,"source":"dbSNP"},{"seq_region_name":"7","id":"rs73483934","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140575670,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575670,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1585670358","clinical_significance":[],"start":140575674,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140575674,"strand":1,"feature_type":"variation"},{"end":140575678,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140575678,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs182751758","clinical_significance":[]},{"id":"rs960271726","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575680,"source":"dbSNP","strand":1,"feature_type":"variation","end":140575680,"alleles":["T","C","G"]},{"seq_region_name":"7","id":"rs1232161984","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140575681,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575681,"source":"dbSNP"},{"alleles":["C","T"],"end":140575684,"feature_type":"variation","strand":1,"source":"dbSNP","start":140575684,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs991426003"},{"clinical_significance":[],"id":"rs1351291604","seq_region_name":"7","alleles":["C","-"],"end":140575684,"feature_type":"variation","strand":1,"source":"dbSNP","start":140575684,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1798268601","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140575689,"alleles":["CC","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575688,"source":"dbSNP"},{"alleles":["C","T"],"end":140575689,"feature_type":"variation","strand":1,"source":"dbSNP","start":140575689,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1236574004"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140575690,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575690,"clinical_significance":[],"seq_region_name":"7","id":"rs150331836"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140575691,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575691,"source":"dbSNP","seq_region_name":"7","id":"rs1326358738","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs948070653","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575695,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140575695},{"feature_type":"variation","strand":1,"end":140575696,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575696,"clinical_significance":[],"seq_region_name":"7","id":"rs1392572267"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575705,"feature_type":"variation","strand":1,"end":140575705,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1388292286"},{"clinical_significance":[],"seq_region_name":"7","id":"rs984733458","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140575706,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575706},{"end":140575707,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140575707,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs909324976"},{"seq_region_name":"7","id":"rs1410766321","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575710,"source":"dbSNP","strand":1,"feature_type":"variation","end":140575710,"alleles":["A","G"]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140575714,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575714,"clinical_significance":[],"seq_region_name":"7","id":"rs2130616858"},{"strand":1,"feature_type":"variation","end":140575715,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575715,"source":"dbSNP","seq_region_name":"7","id":"rs868650059","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798269808","clinical_significance":[],"alleles":["G","A"],"end":140575719,"strand":1,"feature_type":"variation","start":140575719,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798269904","end":140575720,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140575720,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1798270018","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575727,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140575727},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575731,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C","T"],"end":140575731,"seq_region_name":"7","id":"rs1311472777","clinical_significance":[]},{"seq_region_name":"7","id":"rs940766288","clinical_significance":[],"start":140575732,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140575732,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1157392488","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140575733,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575733,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs541647102","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140575734,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575734},{"clinical_significance":[],"seq_region_name":"7","id":"rs994861355","feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140575738,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575738},{"seq_region_name":"7","id":"rs1455257091","clinical_significance":[],"strand":1,"feature_type":"variation","end":140575740,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575740,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1228932259","clinical_significance":[],"start":140575741,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140575741,"strand":1,"feature_type":"variation"},{"start":140575747,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140575747,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1212513918","clinical_significance":[]},{"source":"dbSNP","start":140575749,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140575750,"alleles":["CC","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1563152829"},{"seq_region_name":"7","id":"rs1026709174","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140575750,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575750,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575753,"source":"dbSNP","strand":1,"feature_type":"variation","end":140575753,"alleles":["A","C"],"seq_region_name":"7","id":"rs1798271319","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575762,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140575762,"seq_region_name":"7","id":"rs950851347","clinical_significance":[]},{"id":"rs137989477","seq_region_name":"7","clinical_significance":[],"start":140575763,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140575763,"strand":1,"feature_type":"variation"},{"end":140575765,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140575765,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs902006370","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1236295019","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575766,"source":"dbSNP","strand":1,"feature_type":"variation","end":140575766,"alleles":["G","A","C"]},{"id":"rs1019156858","seq_region_name":"7","clinical_significance":[],"alleles":["C","A"],"end":140575770,"strand":1,"feature_type":"variation","start":140575770,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798272055","alleles":["C","T"],"end":140575771,"feature_type":"variation","strand":1,"source":"dbSNP","start":140575771,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["G","A"],"end":140575773,"strand":1,"feature_type":"variation","start":140575773,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs964870012","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs149502191","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140575780,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575780,"source":"dbSNP"},{"id":"rs545830053","seq_region_name":"7","clinical_significance":[],"alleles":["G","C"],"end":140575786,"strand":1,"feature_type":"variation","start":140575786,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["AAACCCCAGT","-"],"end":140575799,"strand":1,"feature_type":"variation","start":140575790,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1346993390","clinical_significance":[]},{"clinical_significance":[],"id":"rs1316358475","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140575795,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575795},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140575799,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575799,"source":"dbSNP","seq_region_name":"7","id":"rs1798272720","clinical_significance":[]},{"start":140575802,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140575802,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs144040271","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140575805,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575805,"clinical_significance":[],"seq_region_name":"7","id":"rs1563152866"},{"seq_region_name":"7","id":"rs1563152868","clinical_significance":[],"strand":1,"feature_type":"variation","end":140575806,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575806,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1193231406","clinical_significance":[],"start":140575813,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140575813,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"id":"rs889337075","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140575821,"strand":1,"feature_type":"variation","start":140575821,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1175900513","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140575823,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575823},{"start":140575829,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140575829,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1433320284","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575830,"source":"dbSNP","strand":1,"feature_type":"variation","end":140575830,"alleles":["G","A","C"],"id":"rs1798273641","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140575836,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140575836,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1392842579"},{"clinical_significance":[],"id":"rs1192673038","seq_region_name":"7","alleles":["T","C"],"end":140575839,"feature_type":"variation","strand":1,"source":"dbSNP","start":140575839,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1475549819","seq_region_name":"7","alleles":["CC","C"],"end":140575844,"feature_type":"variation","strand":1,"source":"dbSNP","start":140575843,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798274088","source":"dbSNP","start":140575847,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140575847,"feature_type":"variation","strand":1},{"alleles":["C","G","T"],"end":140575851,"feature_type":"variation","strand":1,"source":"dbSNP","start":140575851,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1011264244","seq_region_name":"7"},{"start":140575853,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140575853,"strand":1,"feature_type":"variation","id":"rs1798274403","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798274529","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140575856,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575856},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575860,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140575860,"seq_region_name":"7","id":"rs1021280064","clinical_significance":[]},{"start":140575861,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G","T"],"end":140575861,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs269225","clinical_significance":[]},{"start":140575862,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140575862,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1563152904","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575867,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140575867,"clinical_significance":[],"id":"rs1798275130","seq_region_name":"7"},{"seq_region_name":"7","id":"rs2130617244","clinical_significance":[],"start":140575869,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140575869,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"alleles":["C","A"],"end":140575874,"feature_type":"variation","strand":1,"source":"dbSNP","start":140575874,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798275252"},{"clinical_significance":[],"id":"rs998605372","seq_region_name":"7","source":"dbSNP","start":140575877,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140575877,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1798278068","seq_region_name":"7","source":"dbSNP","start":140575884,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140575884,"alleles":["G","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798278246","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575886,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140575886},{"alleles":["C","T"],"end":140575893,"strand":1,"feature_type":"variation","start":140575893,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1798278428","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575894,"feature_type":"variation","strand":1,"end":140575894,"alleles":["A","G"],"clinical_significance":[],"id":"rs1414900729","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140575895,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575895,"source":"dbSNP","seq_region_name":"7","id":"rs1798278819","clinical_significance":[]},{"seq_region_name":"7","id":"rs1563152917","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["GG","G"],"end":140575896,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575895,"source":"dbSNP"},{"seq_region_name":"7","id":"rs978471292","clinical_significance":[],"start":140575897,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140575897,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"alleles":["G","A","C"],"end":140575898,"strand":1,"feature_type":"variation","start":140575898,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1215348169","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575899,"source":"dbSNP","strand":1,"feature_type":"variation","end":140575899,"alleles":["G","A"],"seq_region_name":"7","id":"rs1455680850","clinical_significance":[]},{"id":"rs1798279710","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140575900,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575900,"source":"dbSNP"},{"source":"dbSNP","start":140575904,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140575904,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1798279841","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1798279975","clinical_significance":[],"start":140575908,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140575908,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575912,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140575912,"seq_region_name":"7","id":"rs1798280112","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575915,"source":"dbSNP","strand":1,"feature_type":"variation","end":140575915,"alleles":["G","C"],"id":"rs1798280246","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs269224","clinical_significance":[],"alleles":["T","A","C"],"end":140575917,"strand":1,"feature_type":"variation","start":140575917,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140575918,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140575918,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs959910221","seq_region_name":"7"},{"clinical_significance":[],"id":"rs2130617389","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140575920,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575920},{"clinical_significance":[],"id":"rs1356652505","seq_region_name":"7","end":140575927,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140575927,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1733108699","clinical_significance":[],"start":140575930,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140575930,"strand":1,"feature_type":"variation"},{"alleles":["G","T"],"end":140575932,"feature_type":"variation","strand":1,"source":"dbSNP","start":140575932,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs934456887"},{"seq_region_name":"7","id":"rs1056802299","clinical_significance":[],"end":140575933,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140575933,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140575934,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575934,"source":"dbSNP","seq_region_name":"7","id":"rs1017959719","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140575935,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575935,"clinical_significance":[],"seq_region_name":"7","id":"rs1798281208"},{"alleles":["CCCCC","CCCC"],"end":140575939,"feature_type":"variation","strand":1,"source":"dbSNP","start":140575935,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798281301"},{"id":"rs1291503337","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140575936,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575936,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575937,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140575937,"clinical_significance":[],"seq_region_name":"7","id":"rs1798281545"},{"clinical_significance":[],"id":"rs1798281672","seq_region_name":"7","end":140575938,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140575938,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs269223","alleles":["C","A","T"],"end":140575939,"feature_type":"variation","strand":1,"source":"dbSNP","start":140575939,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1798282003","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140575944,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575944,"source":"dbSNP"},{"end":140575947,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140575947,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798282133"},{"start":140575951,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140575951,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1410304200","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130617514","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575952,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140575952},{"clinical_significance":[],"id":"rs1798282389","seq_region_name":"7","alleles":["C","G"],"end":140575955,"feature_type":"variation","strand":1,"source":"dbSNP","start":140575955,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575956,"source":"dbSNP","strand":1,"feature_type":"variation","end":140575956,"alleles":["A","G"],"id":"rs917120699","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140575960,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140575960,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798282624"},{"source":"dbSNP","start":140575961,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140575961,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1022900563"},{"seq_region_name":"7","id":"rs1348633557","clinical_significance":[],"start":140575968,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["-","A"],"end":140575967,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140575968,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575968,"clinical_significance":[],"seq_region_name":"7","id":"rs1421282490"},{"clinical_significance":[],"seq_region_name":"7","id":"rs34179994","source":"dbSNP","start":140575969,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AAAAAAAAA","AAAA","AAAAAAAA","AAAAAAAAAA","AAAAAAAAAAA","AAAAAAAAAAAA","AAAAAAAAAAAAA","AAAAAAAAAAAAAA"],"end":140575977,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs867057137","end":140575974,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140575974,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1189915329","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575975,"source":"dbSNP","strand":1,"feature_type":"variation","end":140575989,"alleles":["AAATAAATAAATAAA","AAATAAATAAA"]},{"start":140575976,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["-","G","T"],"end":140575975,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798283747","clinical_significance":[]},{"source":"dbSNP","start":140575976,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140575980,"alleles":["AATAA","AA"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798283902"},{"clinical_significance":[],"id":"rs269222","seq_region_name":"7","source":"dbSNP","start":140575978,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140575978,"alleles":["T","A","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs202125941","seq_region_name":"7","alleles":["T","-"],"end":140575978,"feature_type":"variation","strand":1,"source":"dbSNP","start":140575978,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140575981,"alleles":["AAA","AAAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140575979,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1554471988"},{"feature_type":"variation","strand":1,"end":140575981,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575981,"clinical_significance":[],"id":"rs1044178593","seq_region_name":"7"},{"start":140575982,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140575982,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs547653073","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798284801","source":"dbSNP","start":140575983,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140575985,"alleles":["AAA","AAAA"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575985,"feature_type":"variation","strand":1,"end":140575985,"alleles":["A","T"],"clinical_significance":[],"id":"rs1271232427","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798285032","alleles":["AAACAAA","AAA"],"end":140575993,"feature_type":"variation","strand":1,"source":"dbSNP","start":140575987,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140575992,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140575992,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798285154"},{"feature_type":"variation","strand":1,"end":140576001,"alleles":["AACTTAA","AA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140575995,"clinical_significance":[],"seq_region_name":"7","id":"rs1798285276"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575997,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140575997,"id":"rs187401568","seq_region_name":"7","clinical_significance":[]},{"id":"rs1214031753","seq_region_name":"7","clinical_significance":[],"start":140575998,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140575998,"alleles":["T","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1798285657","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140575999,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140575999},{"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140576002,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576002,"source":"dbSNP","seq_region_name":"7","id":"rs2130617784","clinical_significance":[]},{"seq_region_name":"7","id":"rs1183402704","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576003,"source":"dbSNP","strand":1,"feature_type":"variation","end":140576003,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1798285913","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576005,"source":"dbSNP","strand":1,"feature_type":"variation","end":140576005,"alleles":["A","G"]},{"start":140576008,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140576008,"alleles":["G","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1295226258","clinical_significance":[]},{"id":"rs1798286145","seq_region_name":"7","clinical_significance":[],"start":140576009,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140576009,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140576010,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140576010,"clinical_significance":[],"seq_region_name":"7","id":"rs909209156"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798286429","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140576017,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140576017},{"clinical_significance":[],"seq_region_name":"7","id":"rs566605007","alleles":["G","T"],"end":140576018,"feature_type":"variation","strand":1,"source":"dbSNP","start":140576018,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140576019,"feature_type":"variation","strand":1,"end":140576025,"alleles":["TTCTTTC","TTC"],"clinical_significance":[],"seq_region_name":"7","id":"rs1798286748"},{"alleles":["A","ATA"],"end":140576026,"strand":1,"feature_type":"variation","start":140576026,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798286850","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1413058828","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140576027,"feature_type":"variation","strand":1,"end":140576027,"alleles":["G","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140576028,"feature_type":"variation","strand":1,"alleles":["A","AGATA"],"end":140576028,"clinical_significance":[],"seq_region_name":"7","id":"rs371171534"},{"id":"rs202205552","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576028,"source":"dbSNP","strand":1,"feature_type":"variation","end":140576044,"alleles":["ATATATATATATATATA","ATATATATATATA","ATATATATATATATA","ATATATATATATATATATA","ATATATATATATATATATATA","ATATATATATATATATATATATA","ATATATATATATATATATATATATA","ATATATATATATATATATATATATATA","ATATATATATATATATATATATATATATATA","ATATATATATATATATATATATATATATATATA","ATATATATATATATATATATATATATATATATATA","ATATATATATATATATATATATATATATATATATATA"]},{"id":"rs1585671289","seq_region_name":"7","clinical_significance":[],"start":140576029,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140576029,"strand":1,"feature_type":"variation"},{"id":"rs1481518012","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576032,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140576032},{"feature_type":"variation","strand":1,"end":140576034,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140576034,"clinical_significance":[],"seq_region_name":"7","id":"rs1798288000"},{"alleles":["T","C"],"end":140576037,"strand":1,"feature_type":"variation","start":140576037,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs972176058","clinical_significance":[]},{"end":140576046,"alleles":["ATAAT","ATAATAAT"],"strand":1,"feature_type":"variation","start":140576042,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1585671311","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs539489090","clinical_significance":[],"end":140576043,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140576043,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140576044,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140576044,"alleles":["A","ATATATAAA"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs886428682","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1554472030","clinical_significance":[],"start":140576044,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140576045,"alleles":["AA","AAAA"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1176634742","alleles":["TTATTTTT","T"],"end":140576053,"feature_type":"variation","strand":1,"source":"dbSNP","start":140576046,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1275058418","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140576050,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140576050},{"clinical_significance":[],"seq_region_name":"7","id":"rs868374374","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140576053,"feature_type":"variation","strand":1,"end":140576053,"alleles":["T","C"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576058,"source":"dbSNP","strand":1,"feature_type":"variation","end":140576058,"alleles":["C","A"],"seq_region_name":"7","id":"rs933515288","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140576061,"alleles":["ATT","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576059,"source":"dbSNP","seq_region_name":"7","id":"rs1231544179","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798290037","clinical_significance":[],"strand":1,"feature_type":"variation","end":140576061,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576061,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1334762227","end":140576065,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140576065,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140576066,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TTTTTT","TTTTTTT"],"end":140576071,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798290245"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576067,"source":"dbSNP","strand":1,"feature_type":"variation","end":140576067,"alleles":["T","A"],"seq_region_name":"7","id":"rs1308385218","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798290502","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140576070,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140576070},{"id":"rs1798290610","seq_region_name":"7","clinical_significance":[],"start":140576075,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140576075,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"start":140576079,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140576079,"strand":1,"feature_type":"variation","id":"rs1798290730","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs548227816","clinical_significance":[],"start":140576081,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140576081,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1798290941","clinical_significance":[],"start":140576082,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140576082,"strand":1,"feature_type":"variation"},{"alleles":["C","A","T"],"end":140576084,"strand":1,"feature_type":"variation","start":140576084,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1425737072","clinical_significance":[]},{"end":140576085,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140576085,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs533837405"},{"clinical_significance":[],"seq_region_name":"7","id":"rs772108853","end":140576086,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140576086,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1585671463","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140576088,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576088,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1798291460","clinical_significance":[],"strand":1,"feature_type":"variation","end":140576090,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576090,"source":"dbSNP"},{"source":"dbSNP","start":140576092,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140576092,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1394774660"},{"id":"rs1327321810","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140576094,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576094,"source":"dbSNP"},{"start":140576101,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140576101,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1365238978","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798291909","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576101,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TTT","TT"],"end":140576103},{"source":"dbSNP","start":140576103,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140576103,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798292011"},{"source":"dbSNP","start":140576105,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140576105,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798292116"},{"seq_region_name":"7","id":"rs1459479120","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576107,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140576107},{"start":140576110,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TTTTTT","TTTTTTT"],"end":140576115,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1349202015","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140576111,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576111,"source":"dbSNP","id":"rs1430166468","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140576122,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TTTGTTT","TTT"],"end":140576128,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798292520"},{"seq_region_name":"7","id":"rs369867899","clinical_significance":[],"strand":1,"feature_type":"variation","end":140576126,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576126,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1368573478","seq_region_name":"7","source":"dbSNP","start":140576132,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140576132,"feature_type":"variation","strand":1},{"alleles":["T","C"],"end":140576133,"feature_type":"variation","strand":1,"source":"dbSNP","start":140576133,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1775938679","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140576134,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140576134,"clinical_significance":[],"id":"rs558605944","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1798292970","seq_region_name":"7","alleles":["T","A"],"end":140576140,"feature_type":"variation","strand":1,"source":"dbSNP","start":140576140,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140576146,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140576146,"clinical_significance":[],"seq_region_name":"7","id":"rs193162591"},{"start":140576147,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140576147,"alleles":["G","-"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1405472937","clinical_significance":[]},{"alleles":["TTTTT","TTTT"],"end":140576152,"strand":1,"feature_type":"variation","start":140576148,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798293328","clinical_significance":[]},{"seq_region_name":"7","id":"rs902856403","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576153,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140576153},{"end":140576156,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140576156,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1454830881"},{"seq_region_name":"7","id":"rs1255200592","clinical_significance":[],"end":140576157,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140576157,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140576158,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140576158,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798293756"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140576163,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140576163,"clinical_significance":[],"id":"rs998490805","seq_region_name":"7"},{"end":140576164,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140576164,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798293954","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1554472062","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140576165,"feature_type":"variation","strand":1,"end":140576165,"alleles":["G","A"]},{"clinical_significance":[],"id":"rs2130618382","seq_region_name":"7","alleles":["A","C"],"end":140576166,"feature_type":"variation","strand":1,"source":"dbSNP","start":140576166,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798294174","feature_type":"variation","strand":1,"end":140576168,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140576168},{"id":"rs1380738959","seq_region_name":"7","clinical_significance":[],"start":140576170,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140576170,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1488224762","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576171,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140576171},{"end":140576173,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140576173,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1261408362","clinical_significance":[]},{"seq_region_name":"7","id":"rs1035460339","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576174,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140576174},{"clinical_significance":[],"seq_region_name":"7","id":"rs895533367","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140576175,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140576175},{"seq_region_name":"7","id":"rs1798294801","clinical_significance":[],"strand":1,"feature_type":"variation","end":140576182,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576182,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1306660930","clinical_significance":[],"strand":1,"feature_type":"variation","end":140576192,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576192,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576195,"source":"dbSNP","strand":1,"feature_type":"variation","end":140576195,"alleles":["T","C"],"seq_region_name":"7","id":"rs73483942","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1371278656","feature_type":"variation","strand":1,"end":140576204,"alleles":["TTT","TT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140576202},{"clinical_significance":[],"seq_region_name":"7","id":"rs1311531976","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140576215,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140576215},{"strand":1,"feature_type":"variation","end":140576221,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576221,"source":"dbSNP","id":"rs1798295396","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140576223,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140576223,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798295510"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1438053383","feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140576224,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140576224},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576230,"source":"dbSNP","strand":1,"feature_type":"variation","end":140576230,"alleles":["A","T"],"seq_region_name":"7","id":"rs1342515645","clinical_significance":[]},{"seq_region_name":"7","id":"rs1366232233","clinical_significance":[],"alleles":["T","C"],"end":140576237,"strand":1,"feature_type":"variation","start":140576237,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["G","C"],"end":140576238,"strand":1,"feature_type":"variation","start":140576238,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1288976526","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140576242,"feature_type":"variation","strand":1,"end":140576242,"alleles":["T","A","G"],"clinical_significance":[],"id":"rs745973669","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140576255,"feature_type":"variation","strand":1,"alleles":["ATAATAA","ATAA"],"end":140576261,"clinical_significance":[],"seq_region_name":"7","id":"rs1277228845"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1435147188","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140576256,"feature_type":"variation","strand":1,"end":140576256,"alleles":["T","A","C"]},{"seq_region_name":"7","id":"rs1798296471","clinical_significance":[],"end":140576260,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140576260,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798296577","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140576263,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140576263},{"seq_region_name":"7","id":"rs150800586","clinical_significance":[],"end":140576268,"alleles":["A","-"],"strand":1,"feature_type":"variation","start":140576268,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140576268,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140576268,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1191929709","clinical_significance":[]},{"seq_region_name":"7","id":"rs1204473346","clinical_significance":[],"strand":1,"feature_type":"variation","end":140576274,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576274,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1238071289","source":"dbSNP","start":140576276,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140576276,"alleles":["A","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1473803385","clinical_significance":[],"end":140576278,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140576278,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576279,"source":"dbSNP","strand":1,"feature_type":"variation","end":140576279,"alleles":["T","C","G"],"seq_region_name":"7","id":"rs766143996","clinical_significance":[]},{"source":"dbSNP","start":140576280,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140576280,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1262430987"},{"seq_region_name":"7","id":"rs1563153212","clinical_significance":[],"strand":1,"feature_type":"variation","end":140576281,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576281,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140576288,"feature_type":"variation","strand":1,"end":140576288,"alleles":["T","A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1188368748"},{"clinical_significance":[],"seq_region_name":"7","id":"rs185376389","source":"dbSNP","start":140576290,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A","C"],"end":140576290,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs948449143","end":140576292,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140576292,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140576296,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140576296,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs979928160","clinical_significance":[]},{"seq_region_name":"7","id":"rs1278666390","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140576298,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576298,"source":"dbSNP"},{"id":"rs1230565250","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140576300,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576300,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140576303,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576303,"source":"dbSNP","id":"rs1015426189","seq_region_name":"7","clinical_significance":[]},{"id":"rs574639215","seq_region_name":"7","clinical_significance":[],"start":140576304,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140576304,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140576312,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140576312,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798298814"},{"source":"dbSNP","start":140576315,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140576315,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798299001"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140576318,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576318,"source":"dbSNP","seq_region_name":"7","id":"rs1798299187","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576320,"source":"dbSNP","strand":1,"feature_type":"variation","end":140576320,"alleles":["T","C"],"id":"rs1798299302","seq_region_name":"7","clinical_significance":[]},{"end":140576324,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140576324,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs962025416","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140576333,"alleles":["AAAAAAA","AAAAAA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576327,"source":"dbSNP","seq_region_name":"7","id":"rs1798299568","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs972443906","end":140576331,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140576331,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140576332,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140576332,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585671936"},{"alleles":["T","C"],"end":140576335,"feature_type":"variation","strand":1,"source":"dbSNP","start":140576335,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs923397274","seq_region_name":"7"},{"end":140576336,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140576336,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798299908"},{"seq_region_name":"7","id":"rs1415345726","clinical_significance":[],"start":140576337,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140576337,"alleles":["T","A","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798300150","source":"dbSNP","start":140576340,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140576340,"alleles":["C","G"],"feature_type":"variation","strand":1},{"end":140576349,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","start":140576349,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1409251249","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798300418","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140576356,"feature_type":"variation","strand":1,"end":140576356,"alleles":["T","C"]},{"start":140576360,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140576360,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs886316649","clinical_significance":[]},{"end":140576362,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140576362,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1334717596"},{"source":"dbSNP","start":140576364,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140576364,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798300747"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140576367,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140576367,"clinical_significance":[],"id":"rs1798300848","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140576370,"feature_type":"variation","strand":1,"end":140576370,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1373909869"},{"source":"dbSNP","start":140576376,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140576376,"alleles":["C","A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1172612960"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798301182","source":"dbSNP","start":140576379,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140576379,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1798301291","clinical_significance":[],"alleles":["A","G"],"end":140576381,"strand":1,"feature_type":"variation","start":140576381,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140576385,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140576385,"clinical_significance":[],"seq_region_name":"7","id":"rs944698886"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798301527","source":"dbSNP","start":140576391,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140576391,"alleles":["G","A"],"feature_type":"variation","strand":1},{"start":140576401,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140576401,"alleles":["A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798301634","clinical_significance":[]},{"clinical_significance":[],"id":"rs1798301727","seq_region_name":"7","source":"dbSNP","start":140576405,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140576405,"alleles":["T","C"],"feature_type":"variation","strand":1},{"end":140576414,"alleles":["TTTATTTATT","TTTATT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140576405,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs779204472"},{"clinical_significance":[],"seq_region_name":"7","id":"rs954938369","end":140576406,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140576406,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1040371255","alleles":["A","G"],"end":140576415,"feature_type":"variation","strand":1,"source":"dbSNP","start":140576415,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140576418,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140576418,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798302235","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs147457314","end":140576422,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140576422,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs754621891","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140576423,"feature_type":"variation","strand":1,"end":140576423,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1798302587","clinical_significance":[],"start":140576425,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140576425,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1335566046","feature_type":"variation","strand":1,"end":140576436,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140576436},{"start":140576439,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140576439,"alleles":["A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798302830","clinical_significance":[]},{"seq_region_name":"7","id":"rs1365398430","clinical_significance":[],"end":140576441,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140576441,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs553672971","seq_region_name":"7","clinical_significance":[],"start":140576442,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A","C"],"end":140576442,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140576447,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576447,"source":"dbSNP","seq_region_name":"7","id":"rs1798303234","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs947500698","source":"dbSNP","start":140576451,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140576451,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140576460,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140576460,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1043338922"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140576461,"feature_type":"variation","strand":1,"end":140576465,"alleles":["CCCCC","CCCC"],"clinical_significance":[],"seq_region_name":"7","id":"rs1563153296"},{"id":"rs1798303659","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576466,"source":"dbSNP","strand":1,"feature_type":"variation","end":140576466,"alleles":["A","C"]},{"strand":1,"feature_type":"variation","end":140576467,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576467,"source":"dbSNP","seq_region_name":"7","id":"rs1300216370","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798303878","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576474,"source":"dbSNP","strand":1,"feature_type":"variation","end":140576475,"alleles":["TT","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1315473187","source":"dbSNP","start":140576478,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140576478,"alleles":["C","A","G"],"feature_type":"variation","strand":1},{"alleles":["C","A"],"end":140576479,"feature_type":"variation","strand":1,"source":"dbSNP","start":140576479,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1585672136","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798304220","source":"dbSNP","start":140576480,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TT","T"],"end":140576481,"feature_type":"variation","strand":1},{"id":"rs1337875208","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140576482,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576482,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1233750585","source":"dbSNP","start":140576483,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140576483,"alleles":["T","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1357301330","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576486,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140576486},{"seq_region_name":"7","id":"rs780881735","clinical_significance":[],"strand":1,"feature_type":"variation","end":140576510,"alleles":["A","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576510,"source":"dbSNP"},{"alleles":["C","T"],"end":140576512,"strand":1,"feature_type":"variation","start":140576512,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1798304789","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140576514,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140576514,"clinical_significance":[],"seq_region_name":"7","id":"rs1214397015"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1300170524","source":"dbSNP","start":140576515,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140576515,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140576516,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TT","TTT"],"end":140576517,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1798305081","seq_region_name":"7"},{"clinical_significance":[],"id":"rs572224472","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140576520,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140576520},{"id":"rs1444696540","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576521,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140576521},{"seq_region_name":"7","id":"rs1208042468","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576523,"source":"dbSNP","strand":1,"feature_type":"variation","end":140576523,"alleles":["G","A","C"]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140576524,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140576524,"clinical_significance":[],"seq_region_name":"7","id":"rs1022490983"},{"seq_region_name":"7","id":"rs2130619203","clinical_significance":[],"end":140576527,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140576527,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs189250417","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140576529,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140576529},{"source":"dbSNP","start":140576532,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140576532,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798305781"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576538,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140576538,"seq_region_name":"7","id":"rs1798305891","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585672278","source":"dbSNP","start":140576541,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140576541,"alleles":["T","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1187280130","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140576542,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140576542},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140576546,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576546,"source":"dbSNP","seq_region_name":"7","id":"rs1438804874","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798306498","clinical_significance":[],"alleles":["C","T"],"end":140576547,"strand":1,"feature_type":"variation","start":140576547,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1253130216","alleles":["C","G","T"],"end":140576549,"feature_type":"variation","strand":1,"source":"dbSNP","start":140576549,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1798306813","clinical_significance":[],"strand":1,"feature_type":"variation","end":140576551,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576551,"source":"dbSNP"},{"end":140576556,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140576556,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130619266","clinical_significance":[]},{"end":140576557,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140576557,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1456173219"},{"clinical_significance":[],"id":"rs1798307127","seq_region_name":"7","source":"dbSNP","start":140576559,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140576559,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs904011277","alleles":["A","G"],"end":140576561,"feature_type":"variation","strand":1,"source":"dbSNP","start":140576561,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140576568,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140576568,"clinical_significance":[],"id":"rs1798307474","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140576569,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140576569,"clinical_significance":[],"seq_region_name":"7","id":"rs1798307659"},{"seq_region_name":"7","id":"rs1798307829","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576571,"source":"dbSNP","strand":1,"feature_type":"variation","end":140576571,"alleles":["C","T"]},{"source":"dbSNP","start":140576573,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140576573,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1190779432","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798308161","feature_type":"variation","strand":1,"end":140576577,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140576577},{"feature_type":"variation","strand":1,"end":140576588,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140576588,"clinical_significance":[],"id":"rs1057183848","seq_region_name":"7"},{"id":"rs895596337","seq_region_name":"7","clinical_significance":[],"alleles":["G","A","T"],"end":140576589,"strand":1,"feature_type":"variation","start":140576589,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1013072698","feature_type":"variation","strand":1,"end":140576595,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140576595},{"strand":1,"feature_type":"variation","end":140576596,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576596,"source":"dbSNP","id":"rs1173015416","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1336080309","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140576599,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576599,"source":"dbSNP"},{"start":140576607,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140576607,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798309207","clinical_significance":[]},{"clinical_significance":[],"id":"rs1308922093","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140576609,"feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140576609},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798309574","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140576612,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140576612},{"clinical_significance":[],"id":"rs1427164284","seq_region_name":"7","source":"dbSNP","start":140576613,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140576613,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798309896","feature_type":"variation","strand":1,"end":140576614,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140576614},{"seq_region_name":"7","id":"rs1044276407","clinical_significance":[],"alleles":["G","A"],"end":140576615,"strand":1,"feature_type":"variation","start":140576615,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140576618,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576618,"source":"dbSNP","seq_region_name":"7","id":"rs1031674029","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140576625,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140576625,"clinical_significance":[],"seq_region_name":"7","id":"rs1585672453"},{"id":"rs1798310340","seq_region_name":"7","clinical_significance":[],"end":140576627,"alleles":["TT","T"],"strand":1,"feature_type":"variation","start":140576626,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140576627,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140576627,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1798310462","seq_region_name":"7"},{"alleles":["A","C"],"end":140576629,"feature_type":"variation","strand":1,"source":"dbSNP","start":140576629,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs139901410"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798310691","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140576630,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140576630},{"clinical_significance":[],"seq_region_name":"7","id":"rs1392881087","source":"dbSNP","start":140576634,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140576634,"alleles":["C","A"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576635,"source":"dbSNP","strand":1,"feature_type":"variation","end":140576638,"alleles":["TTTT","TTT"],"seq_region_name":"7","id":"rs1163134661","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140576637,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576637,"source":"dbSNP","id":"rs1798311011","seq_region_name":"7","clinical_significance":[]},{"start":140576639,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140576639,"alleles":["C","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798311097","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1175003647","source":"dbSNP","start":140576640,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140576640,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140576649,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576649,"source":"dbSNP","seq_region_name":"7","id":"rs992470605","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798311377","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140576651,"feature_type":"variation","strand":1,"end":140576651,"alleles":["A","G","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576652,"source":"dbSNP","strand":1,"feature_type":"variation","end":140576652,"alleles":["T","C"],"id":"rs1798311625","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1005307735","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140576668,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140576668},{"alleles":["T","A"],"end":140576669,"feature_type":"variation","strand":1,"source":"dbSNP","start":140576669,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1437416947"},{"id":"rs1237256421","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576674,"source":"dbSNP","strand":1,"feature_type":"variation","end":140576674,"alleles":["G","C"]},{"source":"dbSNP","start":140576678,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140576678,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1585672559","seq_region_name":"7"},{"id":"rs1798312494","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140576687,"strand":1,"feature_type":"variation","start":140576687,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798312663","end":140576690,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140576690,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1436762280","source":"dbSNP","start":140576695,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140576695,"feature_type":"variation","strand":1},{"alleles":["A","G"],"end":140576696,"feature_type":"variation","strand":1,"source":"dbSNP","start":140576696,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1318090843"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1325526752","feature_type":"variation","strand":1,"end":140576697,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140576697},{"seq_region_name":"7","id":"rs1798313296","clinical_significance":[],"start":140576699,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140576699,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140576707,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576707,"source":"dbSNP","seq_region_name":"7","id":"rs1798313435","clinical_significance":[]},{"alleles":["G","A"],"end":140576710,"strand":1,"feature_type":"variation","start":140576710,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1287164573","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798314551","clinical_significance":[],"alleles":["T","C"],"end":140576711,"strand":1,"feature_type":"variation","start":140576711,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1023907337","seq_region_name":"7","clinical_significance":[],"start":140576712,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","G"],"end":140576712,"strand":1,"feature_type":"variation"},{"start":140576715,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140576715,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798314901","clinical_significance":[]},{"seq_region_name":"7","id":"rs1262213950","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140576717,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576717,"source":"dbSNP"},{"alleles":["G","A"],"end":140576718,"strand":1,"feature_type":"variation","start":140576718,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs2130619646","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1237765421","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576722,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140576722},{"seq_region_name":"7","id":"rs1798315247","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576724,"source":"dbSNP","strand":1,"feature_type":"variation","end":140576724,"alleles":["A","G"]},{"alleles":["G","T"],"end":140576731,"strand":1,"feature_type":"variation","start":140576731,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs114941362","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798315508","source":"dbSNP","start":140576736,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140576736,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140576750,"feature_type":"variation","strand":1,"end":140576750,"alleles":["C","G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1304498290"},{"alleles":["A","C"],"end":140576751,"feature_type":"variation","strand":1,"source":"dbSNP","start":140576751,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs979811841"},{"alleles":["G","A"],"end":140576752,"strand":1,"feature_type":"variation","start":140576752,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs961253412","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs543443742","source":"dbSNP","start":140576759,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140576759,"feature_type":"variation","strand":1},{"end":140576761,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140576761,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs993535024"},{"seq_region_name":"7","id":"rs1401735652","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576764,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140576764},{"seq_region_name":"7","id":"rs1798316444","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576767,"source":"dbSNP","strand":1,"feature_type":"variation","end":140576767,"alleles":["A","T"]},{"seq_region_name":"7","id":"rs1030732495","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576768,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140576768},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576772,"source":"dbSNP","strand":1,"feature_type":"variation","end":140576772,"alleles":["G","C"],"seq_region_name":"7","id":"rs1798316723","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798316854","clinical_significance":[],"start":140576774,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140576774,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140576777,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576777,"source":"dbSNP","seq_region_name":"7","id":"rs920476342","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798317092","clinical_significance":[],"start":140576780,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140576780,"strand":1,"feature_type":"variation"},{"id":"rs954849113","seq_region_name":"7","clinical_significance":[],"start":140576787,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140576787,"alleles":["G","A","C"],"strand":1,"feature_type":"variation"},{"id":"rs1585672726","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140576791,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576791,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798317488","end":140576792,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140576792,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140576797,"alleles":["AAAAA","AAAA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576793,"source":"dbSNP","id":"rs1329909323","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs983269813","alleles":["A","C","G"],"end":140576794,"feature_type":"variation","strand":1,"source":"dbSNP","start":140576794,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs2130619812","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576795,"source":"dbSNP","strand":1,"feature_type":"variation","end":140576795,"alleles":["A","G"]},{"feature_type":"variation","strand":1,"alleles":["AAGAAG","AAG"],"end":140576801,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140576796,"clinical_significance":[],"id":"rs1798317928","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576798,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140576798,"id":"rs1798318042","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs10227869","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140576800,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140576800},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140576801,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140576801,"clinical_significance":[],"seq_region_name":"7","id":"rs1193830678"},{"seq_region_name":"7","id":"rs1455334112","clinical_significance":[],"start":140576802,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140576802,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140576807,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140576807,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130619860"},{"start":140576807,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140576810,"alleles":["GGGG","GGG"],"strand":1,"feature_type":"variation","id":"rs1798318549","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798318696","alleles":["G","A"],"end":140576809,"feature_type":"variation","strand":1,"source":"dbSNP","start":140576809,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798318811","source":"dbSNP","start":140576810,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140576810,"alleles":["G","A"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140576815,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140576815,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798318932"},{"end":140576822,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140576822,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs269221","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140576823,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576823,"source":"dbSNP","seq_region_name":"7","id":"rs1040423856","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs547984786","source":"dbSNP","start":140576828,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140576828,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs777168860","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140576829,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140576829},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576837,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140576837,"seq_region_name":"7","id":"rs1199230970","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs900492877","source":"dbSNP","start":140576840,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140576840,"alleles":["A","-"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140576840,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140576840,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1248246069"},{"seq_region_name":"7","id":"rs1798320112","clinical_significance":[],"strand":1,"feature_type":"variation","end":140576841,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576841,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140576849,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576849,"source":"dbSNP","seq_region_name":"7","id":"rs1798320250","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140576853,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140576853,"clinical_significance":[],"seq_region_name":"7","id":"rs2130619985"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140576859,"feature_type":"variation","strand":1,"end":140576859,"alleles":["T","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1476976970"},{"feature_type":"variation","strand":1,"end":140576860,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140576860,"clinical_significance":[],"seq_region_name":"7","id":"rs932089014"},{"clinical_significance":[],"seq_region_name":"7","id":"rs978903782","alleles":["C","T"],"end":140576861,"feature_type":"variation","strand":1,"source":"dbSNP","start":140576861,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140576865,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140576865,"clinical_significance":[],"seq_region_name":"7","id":"rs566248078"},{"source":"dbSNP","start":140576867,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140576867,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798320910"},{"source":"dbSNP","start":140576868,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["CA","-"],"end":140576869,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1236688337"},{"end":140576869,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140576869,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1314983321","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576870,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140576870,"seq_region_name":"7","id":"rs903898720","clinical_significance":[]},{"seq_region_name":"7","id":"rs1431655649","clinical_significance":[],"start":140576876,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A","C"],"end":140576876,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798321551","source":"dbSNP","start":140576883,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140576883,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140576884,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140576884,"clinical_significance":[],"seq_region_name":"7","id":"rs1000114322"},{"clinical_significance":[],"seq_region_name":"7","id":"rs749744607","end":140576886,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140576886,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140576889,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140576889,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130620113"},{"clinical_significance":[],"id":"rs771343105","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140576893,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140576893},{"source":"dbSNP","start":140576894,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140576894,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1056833659"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140576895,"feature_type":"variation","strand":1,"end":140576895,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1798322055"},{"end":140576896,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140576896,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs774770368","clinical_significance":[]},{"start":140576905,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140576905,"strand":1,"feature_type":"variation","id":"rs1383726875","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1422696368","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576906,"source":"dbSNP","strand":1,"feature_type":"variation","end":140576906,"alleles":["G","A","C"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140576908,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140576908,"clinical_significance":[],"id":"rs1405603949","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1798323332","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140576909,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576909,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140576914,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576914,"source":"dbSNP","seq_region_name":"7","id":"rs1798323454","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576920,"source":"dbSNP","strand":1,"feature_type":"variation","end":140576920,"alleles":["T","C"],"seq_region_name":"7","id":"rs1798323584","clinical_significance":[]},{"seq_region_name":"7","id":"rs948373798","clinical_significance":[],"start":140576923,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140576923,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798323812","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140576928,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140576928},{"source":"dbSNP","start":140576929,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140576929,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs2130620220","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1798323922","clinical_significance":[],"start":140576931,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140576931,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798324033","feature_type":"variation","strand":1,"end":140576933,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140576933},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140576939,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140576939,"clinical_significance":[],"seq_region_name":"7","id":"rs1044132088"},{"strand":1,"feature_type":"variation","end":140576948,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576948,"source":"dbSNP","seq_region_name":"7","id":"rs1798324249","clinical_significance":[]},{"id":"rs1798324356","seq_region_name":"7","clinical_significance":[],"start":140576953,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140576953,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1475478839","clinical_significance":[],"strand":1,"feature_type":"variation","end":140576956,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576956,"source":"dbSNP"},{"start":140576961,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140576961,"alleles":["T","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130620260","clinical_significance":[]},{"seq_region_name":"7","id":"rs888166514","clinical_significance":[],"strand":1,"feature_type":"variation","end":140576963,"alleles":["T","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140576963,"source":"dbSNP"},{"id":"rs1798324671","seq_region_name":"7","clinical_significance":[],"start":140576964,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140576964,"strand":1,"feature_type":"variation"},{"alleles":["T","C"],"end":140576970,"feature_type":"variation","strand":1,"source":"dbSNP","start":140576970,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1748932791"},{"seq_region_name":"7","id":"rs1798324787","clinical_significance":[],"start":140576973,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140576973,"strand":1,"feature_type":"variation"},{"start":140576976,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140576976,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs941214657","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798325033","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140576986,"feature_type":"variation","strand":1,"end":140576986,"alleles":["G","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs969691110","source":"dbSNP","start":140577003,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C","T"],"end":140577003,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1324577804","alleles":["G","A"],"end":140577007,"feature_type":"variation","strand":1,"source":"dbSNP","start":140577007,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1333219096","alleles":["G","A"],"end":140577008,"feature_type":"variation","strand":1,"source":"dbSNP","start":140577008,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1798325563","clinical_significance":[],"start":140577012,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140577012,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1403542098","clinical_significance":[],"end":140577014,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140577014,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["ACACACA","ACACA"],"end":140577022,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577016,"source":"dbSNP","seq_region_name":"7","id":"rs1798325929","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585673124","clinical_significance":[],"start":140577022,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C","G"],"end":140577022,"strand":1,"feature_type":"variation"},{"alleles":["C","G","T"],"end":140577024,"strand":1,"feature_type":"variation","start":140577024,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs746289140","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798326609","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577026,"source":"dbSNP","strand":1,"feature_type":"variation","end":140577026,"alleles":["T","G"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577029,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140577029,"seq_region_name":"7","id":"rs1036805941","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140577035,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577035,"source":"dbSNP","seq_region_name":"7","id":"rs1027822876","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs551641311","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577036,"feature_type":"variation","strand":1,"end":140577036,"alleles":["T","C"]},{"end":140577037,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140577037,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs897096710","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs772398170","source":"dbSNP","start":140577059,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140577059,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577062,"source":"dbSNP","strand":1,"feature_type":"variation","end":140577062,"alleles":["A","G"],"seq_region_name":"7","id":"rs1218495291","clinical_significance":[]},{"seq_region_name":"7","id":"rs983709795","clinical_significance":[],"start":140577063,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140577063,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"id":"rs1798327942","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140577073,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577073,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1798328071","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140577074,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577074,"source":"dbSNP"},{"start":140577075,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140577075,"alleles":["A","G"],"strand":1,"feature_type":"variation","id":"rs1350140446","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577078,"source":"dbSNP","strand":1,"feature_type":"variation","end":140577078,"alleles":["G","A"],"seq_region_name":"7","id":"rs1446370611","clinical_significance":[]},{"source":"dbSNP","start":140577080,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140577080,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798328404"},{"clinical_significance":[],"id":"rs1357042906","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140577089,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577089},{"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140577090,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577090,"source":"dbSNP","seq_region_name":"7","id":"rs1210693816","clinical_significance":[]},{"alleles":["TT","T"],"end":140577093,"feature_type":"variation","strand":1,"source":"dbSNP","start":140577092,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798329241"},{"source":"dbSNP","start":140577096,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140577096,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs998501083","seq_region_name":"7"},{"start":140577102,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140577102,"alleles":["C","A"],"strand":1,"feature_type":"variation","id":"rs1798329470","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs907684341","seq_region_name":"7","feature_type":"variation","strand":1,"end":140577103,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577103},{"clinical_significance":[],"id":"rs1489786429","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140577107,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577107},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798329820","end":140577114,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140577114,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","G"],"end":140577116,"strand":1,"feature_type":"variation","start":140577116,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798329921","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577118,"feature_type":"variation","strand":1,"end":140577121,"alleles":["AAAT","AAATAAAT"],"clinical_significance":[],"seq_region_name":"7","id":"rs200573701"},{"start":140577121,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140577121,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798330236","clinical_significance":[]},{"clinical_significance":[],"id":"rs1798330385","seq_region_name":"7","source":"dbSNP","start":140577122,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140577122,"alleles":["G","A"],"feature_type":"variation","strand":1},{"end":140577124,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140577124,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs965982492","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563153601","source":"dbSNP","start":140577128,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140577128,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1798330920","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140577129,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577129},{"clinical_significance":[],"seq_region_name":"7","id":"rs975989034","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577130,"feature_type":"variation","strand":1,"end":140577130,"alleles":["A","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577130,"feature_type":"variation","strand":1,"alleles":["A","AA"],"end":140577130,"clinical_significance":[],"seq_region_name":"7","id":"rs1798331252"},{"end":140577131,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140577131,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1252441628","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140577132,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577132,"source":"dbSNP","id":"rs921968138","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798332907","end":140577137,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140577137,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130620577","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140577138,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577138},{"source":"dbSNP","start":140577141,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140577141,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1418572032"},{"start":140577143,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","T"],"end":140577143,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs552258812","clinical_significance":[]},{"end":140577144,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140577144,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798333504"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140577148,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577148,"clinical_significance":[],"seq_region_name":"7","id":"rs1471713791"},{"clinical_significance":[],"id":"rs890462646","seq_region_name":"7","alleles":["C","T"],"end":140577154,"feature_type":"variation","strand":1,"source":"dbSNP","start":140577154,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140577156,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140577156,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs1236700549","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","C"],"end":140577157,"feature_type":"variation","strand":1,"source":"dbSNP","start":140577157,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1007532405"},{"alleles":["T","C"],"end":140577161,"feature_type":"variation","strand":1,"source":"dbSNP","start":140577161,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1473563945"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577170,"source":"dbSNP","strand":1,"feature_type":"variation","end":140577170,"alleles":["G","T"],"id":"rs1798334206","seq_region_name":"7","clinical_significance":[]},{"id":"rs1798334313","seq_region_name":"7","clinical_significance":[],"end":140577171,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140577171,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140577172,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140577172,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798334424","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798334520","alleles":["T","C"],"end":140577177,"feature_type":"variation","strand":1,"source":"dbSNP","start":140577177,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577179,"feature_type":"variation","strand":1,"end":140577179,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1798334629"},{"end":140577181,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140577181,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1798334733","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140577185,"alleles":["C","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577185,"clinical_significance":[],"seq_region_name":"7","id":"rs748373335"},{"seq_region_name":"7","id":"rs1256178823","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577192,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140577192},{"source":"dbSNP","start":140577194,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140577194,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1043699969"},{"id":"rs1362745140","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577194,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GGG","GGGG"],"end":140577196},{"seq_region_name":"7","id":"rs1472896625","clinical_significance":[],"start":140577196,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140577196,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs269220","clinical_significance":[],"start":140577197,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140577197,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798335699","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577202,"feature_type":"variation","strand":1,"end":140577202,"alleles":["G","A"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577215,"source":"dbSNP","strand":1,"feature_type":"variation","end":140577215,"alleles":["C","T"],"seq_region_name":"7","id":"rs2130620755","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140577216,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577216,"source":"dbSNP","seq_region_name":"7","id":"rs1798335914","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798336056","end":140577217,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140577217,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577219,"source":"dbSNP","strand":1,"feature_type":"variation","end":140577219,"alleles":["G","A","T"],"seq_region_name":"7","id":"rs1378840021","clinical_significance":[]},{"clinical_significance":[],"id":"rs968773777","seq_region_name":"7","feature_type":"variation","strand":1,"end":140577220,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577220},{"feature_type":"variation","strand":1,"end":140577221,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577221,"clinical_significance":[],"id":"rs1442407443","seq_region_name":"7"},{"end":140577223,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","start":140577223,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798336487","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140577224,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577224,"clinical_significance":[],"seq_region_name":"7","id":"rs1402092517"},{"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140577225,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577225,"clinical_significance":[],"id":"rs978955009","seq_region_name":"7"},{"seq_region_name":"7","id":"rs935410724","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577226,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140577226},{"clinical_significance":[],"id":"rs2130620816","seq_region_name":"7","end":140577227,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140577227,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1423126148","end":140577228,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140577228,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140577229,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577229,"clinical_significance":[],"seq_region_name":"7","id":"rs1302989483"},{"seq_region_name":"7","id":"rs1371648188","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140577230,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577230,"source":"dbSNP"},{"end":140577233,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140577233,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1464682075","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140577238,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577238,"clinical_significance":[],"id":"rs1798337717","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs761012726","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577240,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140577240},{"seq_region_name":"7","id":"rs1412226873","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140577243,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577243,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577244,"source":"dbSNP","strand":1,"feature_type":"variation","end":140577244,"alleles":["G","A","C"],"seq_region_name":"7","id":"rs1395093825","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577245,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140577245,"clinical_significance":[],"seq_region_name":"7","id":"rs1798338448"},{"end":140577246,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140577246,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1798338638","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577247,"source":"dbSNP","strand":1,"feature_type":"variation","end":140577247,"alleles":["A","G"],"seq_region_name":"7","id":"rs1798338757","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1304911818","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140577248,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577248},{"end":140577252,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140577252,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1335269761"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577254,"feature_type":"variation","strand":1,"end":140577254,"alleles":["T","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1412722196"},{"feature_type":"variation","strand":1,"end":140577258,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577258,"clinical_significance":[],"seq_region_name":"7","id":"rs764189090"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577259,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140577259,"seq_region_name":"7","id":"rs1286141552","clinical_significance":[]},{"start":140577260,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140577263,"alleles":["AAAA","AA","AAA"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798339435","clinical_significance":[]},{"clinical_significance":[],"id":"rs1236653580","seq_region_name":"7","end":140577267,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140577267,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140577268,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140577268,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1178067482"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140577273,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577273,"source":"dbSNP","id":"rs76496482","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs776591665","clinical_significance":[],"end":140577278,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140577278,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1196115808","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577281,"source":"dbSNP","strand":1,"feature_type":"variation","end":140577281,"alleles":["A","C"]},{"source":"dbSNP","start":140577282,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140577282,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs570177272","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1275152817","source":"dbSNP","start":140577283,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140577283,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577283,"feature_type":"variation","strand":1,"alleles":["T","TT"],"end":140577283,"clinical_significance":[],"seq_region_name":"7","id":"rs1798340312"},{"seq_region_name":"7","id":"rs1798340407","clinical_significance":[],"alleles":["A","T"],"end":140577285,"strand":1,"feature_type":"variation","start":140577285,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140577286,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140577286,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798340505","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140577288,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577288,"source":"dbSNP","id":"rs2130621044","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140577289,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577289,"source":"dbSNP","seq_region_name":"7","id":"rs762882148","clinical_significance":[]},{"start":140577291,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140577291,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1219956278","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1244953818","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577292,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140577292},{"start":140577301,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140577301,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1285374182","clinical_significance":[]},{"end":140577305,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140577305,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798341077"},{"strand":1,"feature_type":"variation","end":140577310,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577310,"source":"dbSNP","seq_region_name":"7","id":"rs1225900356","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798341270","alleles":["G","A"],"end":140577311,"feature_type":"variation","strand":1,"source":"dbSNP","start":140577311,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577317,"source":"dbSNP","strand":1,"feature_type":"variation","end":140577317,"alleles":["G","C"],"seq_region_name":"7","id":"rs1563153722","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1275099313","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577318,"feature_type":"variation","strand":1,"alleles":["C","-"],"end":140577318},{"id":"rs1378614576","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577321,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140577321},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577325,"source":"dbSNP","strand":1,"feature_type":"variation","end":140577325,"alleles":["G","A"],"id":"rs1306687836","seq_region_name":"7","clinical_significance":[]},{"id":"rs192285269","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577327,"source":"dbSNP","strand":1,"feature_type":"variation","end":140577327,"alleles":["C","T"]},{"start":140577328,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140577328,"alleles":["A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1045290422","clinical_significance":[]},{"alleles":["TCT","T"],"end":140577331,"strand":1,"feature_type":"variation","start":140577329,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1483974264","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140577334,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140577334,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1294776317","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1194032371","clinical_significance":[],"start":140577337,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140577337,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"alleles":["A","G"],"end":140577340,"strand":1,"feature_type":"variation","start":140577340,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1349290500","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","C"],"end":140577341,"strand":1,"feature_type":"variation","start":140577341,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798342461","clinical_significance":[]},{"alleles":["G","A"],"end":140577343,"strand":1,"feature_type":"variation","start":140577343,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1159564611","clinical_significance":[]},{"alleles":["G","T"],"end":140577347,"feature_type":"variation","strand":1,"source":"dbSNP","start":140577347,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798342661"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577350,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140577350,"clinical_significance":[],"seq_region_name":"7","id":"rs568380365"},{"seq_region_name":"7","id":"rs917472722","clinical_significance":[],"start":140577357,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140577357,"strand":1,"feature_type":"variation"},{"start":140577360,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140577360,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798342983","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798343068","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140577363,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577363},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798343168","alleles":["T","C"],"end":140577372,"feature_type":"variation","strand":1,"source":"dbSNP","start":140577372,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1798343276","clinical_significance":[],"start":140577375,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140577375,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1255746474","feature_type":"variation","strand":1,"end":140577379,"alleles":["T","C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577379},{"source":"dbSNP","start":140577381,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140577381,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1421330926"},{"clinical_significance":[],"id":"rs1378674758","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140577383,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577383},{"alleles":["A","C"],"end":140577384,"strand":1,"feature_type":"variation","start":140577384,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1798343736","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs537609178","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140577394,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577394},{"id":"rs1249797421","seq_region_name":"7","clinical_significance":[],"start":140577394,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TTTTT","TTTTTTTTTT"],"end":140577398,"strand":1,"feature_type":"variation"},{"end":140577396,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140577396,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798344082"},{"start":140577396,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140577402,"alleles":["TTTCTTT","TTT"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798344184","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140577397,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577397,"source":"dbSNP","seq_region_name":"7","id":"rs1269478904","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577398,"feature_type":"variation","strand":1,"end":140577398,"alleles":["T","C"],"clinical_significance":[],"id":"rs1189602864","seq_region_name":"7"},{"seq_region_name":"7","id":"rs28405927","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140577399,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577399,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1798344705","clinical_significance":[],"start":140577399,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","-"],"end":140577399,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1798344813","clinical_significance":[],"alleles":["T","C"],"end":140577400,"strand":1,"feature_type":"variation","start":140577400,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140577400,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140577415,"alleles":["TTTTTTTTTTTTTTTT","TTTTTTTTTT","TTTTTTTTTTTT","TTTTTTTTTTTTT","TTTTTTTTTTTTTT","TTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs60840763","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1285787476","source":"dbSNP","start":140577403,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140577403,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577404,"feature_type":"variation","strand":1,"end":140577404,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1798345446"},{"seq_region_name":"7","id":"rs199657138","clinical_significance":[],"start":140577405,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["-","C"],"end":140577404,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs28626923","feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140577405,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577405},{"strand":1,"feature_type":"variation","end":140577405,"alleles":["-","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577406,"source":"dbSNP","seq_region_name":"7","id":"rs1422871648","clinical_significance":[]},{"clinical_significance":[],"id":"rs909658402","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140577406,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577406},{"clinical_significance":[],"id":"rs1798346159","seq_region_name":"7","end":140577407,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140577407,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140577408,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140577408,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs199560497","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140577409,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["-","C"],"end":140577408,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1563153775"},{"clinical_significance":[],"id":"rs1366786244","seq_region_name":"7","alleles":["G","-"],"end":140577416,"feature_type":"variation","strand":1,"source":"dbSNP","start":140577416,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1383058240","seq_region_name":"7","feature_type":"variation","strand":1,"end":140577416,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577416},{"clinical_significance":[],"id":"rs1401793275","seq_region_name":"7","feature_type":"variation","strand":1,"end":140577417,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577417},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798346831","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577420,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140577420},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577420,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","TT"],"end":140577420,"id":"rs1798346939","seq_region_name":"7","clinical_significance":[]},{"start":140577421,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140577421,"alleles":["G","T"],"strand":1,"feature_type":"variation","id":"rs2130621526","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577421,"feature_type":"variation","strand":1,"end":140577422,"alleles":["GG","G"],"clinical_significance":[],"id":"rs1027299710","seq_region_name":"7"},{"seq_region_name":"7","id":"rs373240056","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577424,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140577424},{"seq_region_name":"7","id":"rs1798347271","clinical_significance":[],"strand":1,"feature_type":"variation","end":140577425,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577425,"source":"dbSNP"},{"alleles":["C","G"],"end":140577426,"feature_type":"variation","strand":1,"source":"dbSNP","start":140577426,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798347384"},{"start":140577428,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","T"],"end":140577428,"strand":1,"feature_type":"variation","id":"rs577658141","seq_region_name":"7","clinical_significance":[]},{"start":140577429,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140577429,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs28390113","clinical_significance":[]},{"end":140577430,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140577430,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1174005158","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798347916","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577434,"source":"dbSNP","strand":1,"feature_type":"variation","end":140577434,"alleles":["G","T"]},{"seq_region_name":"7","id":"rs553574980","clinical_significance":[],"start":140577437,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140577437,"alleles":["G","A","C"],"strand":1,"feature_type":"variation"},{"start":140577440,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140577440,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798348316","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140577447,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577447,"clinical_significance":[],"seq_region_name":"7","id":"rs1391201377"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140577450,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577450,"source":"dbSNP","seq_region_name":"7","id":"rs1432114579","clinical_significance":[]},{"clinical_significance":[],"id":"rs1798348841","seq_region_name":"7","source":"dbSNP","start":140577451,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140577451,"feature_type":"variation","strand":1},{"start":140577456,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140577456,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798349000","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798349194","clinical_significance":[],"end":140577458,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140577458,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1422816358","clinical_significance":[],"alleles":["A","G"],"end":140577462,"strand":1,"feature_type":"variation","start":140577462,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs183745445","clinical_significance":[],"alleles":["C","T"],"end":140577466,"strand":1,"feature_type":"variation","start":140577466,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577467,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140577467,"clinical_significance":[],"seq_region_name":"7","id":"rs1396458441"},{"seq_region_name":"7","id":"rs1212124041","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577471,"source":"dbSNP","strand":1,"feature_type":"variation","end":140577471,"alleles":["A","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798350437","feature_type":"variation","strand":1,"end":140577473,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577473},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140577476,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577476,"clinical_significance":[],"seq_region_name":"7","id":"rs545903851"},{"clinical_significance":[],"id":"rs1798350796","seq_region_name":"7","feature_type":"variation","strand":1,"end":140577477,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577477},{"strand":1,"feature_type":"variation","end":140577478,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577478,"source":"dbSNP","id":"rs1585674167","seq_region_name":"7","clinical_significance":[]},{"end":140577488,"alleles":["ACCTCCACCTC","ACCTC"],"strand":1,"feature_type":"variation","start":140577478,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798351112","clinical_significance":[]},{"seq_region_name":"7","id":"rs111489917","clinical_significance":[],"strand":1,"feature_type":"variation","end":140577479,"alleles":["C","A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577479,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1311052710","end":140577480,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140577480,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140577488,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577488,"clinical_significance":[],"id":"rs1295713602","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs953294613","source":"dbSNP","start":140577489,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C","T"],"end":140577489,"feature_type":"variation","strand":1},{"start":140577490,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","T"],"end":140577490,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs58118476","clinical_significance":[]},{"alleles":["G","A","C","T"],"end":140577491,"feature_type":"variation","strand":1,"source":"dbSNP","start":140577491,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs889689195"},{"feature_type":"variation","strand":1,"end":140577493,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577493,"clinical_significance":[],"seq_region_name":"7","id":"rs1245567518"},{"alleles":["G","C"],"end":140577499,"feature_type":"variation","strand":1,"source":"dbSNP","start":140577499,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798353102"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798353285","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140577510,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577510},{"start":140577511,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140577511,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1404589665","clinical_significance":[]},{"id":"rs1798353527","seq_region_name":"7","clinical_significance":[],"start":140577516,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140577516,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1007590678","clinical_significance":[],"start":140577517,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140577517,"alleles":["C","A","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1465754432","clinical_significance":[],"start":140577518,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140577518,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140577521,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577521,"source":"dbSNP","seq_region_name":"7","id":"rs1798353909","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577522,"feature_type":"variation","strand":1,"end":140577522,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1355118543"},{"clinical_significance":[],"id":"rs1017606310","seq_region_name":"7","source":"dbSNP","start":140577523,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140577523,"alleles":["G","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs543832803","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577525,"source":"dbSNP","strand":1,"feature_type":"variation","end":140577525,"alleles":["G","T"]},{"seq_region_name":"7","id":"rs1798354402","clinical_significance":[],"end":140577527,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140577527,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs561900483","end":140577531,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140577531,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1798354721","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140577532,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577532,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1189061456","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577536,"feature_type":"variation","strand":1,"end":140577536,"alleles":["T","C"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577538,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140577538,"id":"rs1798355030","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140577540,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577540,"clinical_significance":[],"seq_region_name":"7","id":"rs61333130"},{"id":"rs1031717278","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577542,"source":"dbSNP","strand":1,"feature_type":"variation","end":140577542,"alleles":["C","A","T"]},{"id":"rs956411132","seq_region_name":"7","clinical_significance":[],"end":140577543,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140577543,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1164868229","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577547,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140577547},{"source":"dbSNP","start":140577548,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140577548,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798355777"},{"end":140577550,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140577550,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs992982417","clinical_significance":[]},{"end":140577551,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140577551,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs62485834","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140577552,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577552,"clinical_significance":[],"id":"rs1482727741","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs970316909","feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140577554,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577554},{"clinical_significance":[],"seq_region_name":"7","id":"rs541315484","source":"dbSNP","start":140577555,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140577555,"feature_type":"variation","strand":1},{"id":"rs559995733","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577557,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140577557},{"id":"rs1277542544","seq_region_name":"7","clinical_significance":[],"start":140577560,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140577560,"strand":1,"feature_type":"variation"},{"start":140577561,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140577561,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1341996355","clinical_significance":[]},{"id":"rs1798357423","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140577570,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577570,"source":"dbSNP"},{"seq_region_name":"7","id":"rs753501015","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577573,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140577573},{"clinical_significance":[],"seq_region_name":"7","id":"rs1240728921","alleles":["T","A","C"],"end":140577575,"feature_type":"variation","strand":1,"source":"dbSNP","start":140577575,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1395608231","seq_region_name":"7","clinical_significance":[],"end":140577580,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140577580,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs909542546","clinical_significance":[],"start":140577586,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140577586,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs941150759","seq_region_name":"7","end":140577587,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140577587,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140577588,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140577588,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs917958917"},{"seq_region_name":"7","id":"rs1464172610","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577589,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140577589},{"alleles":["G","A","T"],"end":140577590,"feature_type":"variation","strand":1,"source":"dbSNP","start":140577590,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1249560471"},{"seq_region_name":"7","id":"rs2130622103","clinical_significance":[],"start":140577594,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140577594,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577598,"source":"dbSNP","strand":1,"feature_type":"variation","end":140577598,"alleles":["A","G"],"seq_region_name":"7","id":"rs2130622113","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1430628700","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577599,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140577599},{"clinical_significance":[],"id":"rs1168856726","seq_region_name":"7","source":"dbSNP","start":140577604,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140577604,"feature_type":"variation","strand":1},{"alleles":["C","A"],"end":140577605,"strand":1,"feature_type":"variation","start":140577605,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs541735617","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140577606,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577606,"clinical_significance":[],"seq_region_name":"7","id":"rs533606007"},{"alleles":["G","A"],"end":140577609,"strand":1,"feature_type":"variation","start":140577609,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1798359137","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585674524","clinical_significance":[],"start":140577614,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140577614,"alleles":["T","G"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140577617,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140577617,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1798359336","seq_region_name":"7"},{"end":140577618,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","start":140577618,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1367018044","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140577621,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577621,"source":"dbSNP","seq_region_name":"7","id":"rs1798359567","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798359674","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140577624,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577624,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798359790","feature_type":"variation","strand":1,"end":140577628,"alleles":["C","A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577628},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577631,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140577631,"seq_region_name":"7","id":"rs2130622201","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140577635,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577635,"source":"dbSNP","seq_region_name":"7","id":"rs1585674549","clinical_significance":[]},{"source":"dbSNP","start":140577646,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140577646,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130622212"},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140577648,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577648,"clinical_significance":[],"id":"rs149813928","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140577649,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577649,"source":"dbSNP","seq_region_name":"7","id":"rs1798360149","clinical_significance":[]},{"source":"dbSNP","start":140577651,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140577651,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1585674567","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1422873128","clinical_significance":[],"alleles":["C","T"],"end":140577655,"strand":1,"feature_type":"variation","start":140577655,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140577656,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140577656,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798360481","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs949560811","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577657,"feature_type":"variation","strand":1,"alleles":["C","A","G"],"end":140577657},{"seq_region_name":"7","id":"rs564194661","clinical_significance":[],"alleles":["G","A"],"end":140577661,"strand":1,"feature_type":"variation","start":140577661,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140577665,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140577665,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1256901004","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["GGG","GG"],"end":140577668,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577666,"source":"dbSNP","seq_region_name":"7","id":"rs1798361017","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798361166","clinical_significance":[],"start":140577668,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140577668,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1210283431","clinical_significance":[],"start":140577675,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140577675,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"id":"rs1798361378","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140577676,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577676,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798361487","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577677,"feature_type":"variation","strand":1,"end":140577677,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs188462724","alleles":["G","A"],"end":140577678,"feature_type":"variation","strand":1,"source":"dbSNP","start":140577678,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1798361739","seq_region_name":"7","clinical_significance":[],"alleles":["T","G"],"end":140577679,"strand":1,"feature_type":"variation","start":140577679,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1263441221","source":"dbSNP","start":140577680,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140577680,"alleles":["G","C"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140577681,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140577681,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1404033887"},{"seq_region_name":"7","id":"rs1243881239","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577683,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140577683},{"clinical_significance":[],"id":"rs931565365","seq_region_name":"7","source":"dbSNP","start":140577687,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140577687,"feature_type":"variation","strand":1},{"start":140577688,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140577688,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs549767379","clinical_significance":[]},{"id":"rs145834793","seq_region_name":"7","clinical_significance":[],"start":140577689,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140577689,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140577690,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577690,"source":"dbSNP","seq_region_name":"7","id":"rs942587193","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1376201435","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577691,"feature_type":"variation","strand":1,"end":140577691,"alleles":["C","T"]},{"alleles":["C","A","T"],"end":140577696,"feature_type":"variation","strand":1,"source":"dbSNP","start":140577696,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1039094833","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140577702,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577702,"clinical_significance":[],"seq_region_name":"7","id":"rs1388974822"},{"feature_type":"variation","strand":1,"end":140577704,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577704,"clinical_significance":[],"seq_region_name":"7","id":"rs1798363102"},{"seq_region_name":"7","id":"rs1005079820","clinical_significance":[],"alleles":["C","A","T"],"end":140577705,"strand":1,"feature_type":"variation","start":140577705,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1798363357","clinical_significance":[],"start":140577719,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140577719,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs904527881","source":"dbSNP","start":140577722,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140577722,"alleles":["A","G"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577722,"feature_type":"variation","strand":1,"alleles":["AT","-"],"end":140577723,"clinical_significance":[],"id":"rs1454676346","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798363688","source":"dbSNP","start":140577727,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140577727,"alleles":["A","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1798363802","seq_region_name":"7","source":"dbSNP","start":140577732,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140577732,"feature_type":"variation","strand":1},{"start":140577734,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140577734,"alleles":["G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1382575844","clinical_significance":[]},{"id":"rs1798364039","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577735,"source":"dbSNP","strand":1,"feature_type":"variation","end":140577735,"alleles":["C","A","G"]},{"seq_region_name":"7","id":"rs1014685573","clinical_significance":[],"end":140577745,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140577745,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1798364324","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577747,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140577747},{"clinical_significance":[],"seq_region_name":"7","id":"rs901560677","source":"dbSNP","start":140577751,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140577751,"alleles":["C","T"],"feature_type":"variation","strand":1},{"id":"rs535746119","seq_region_name":"7","clinical_significance":[],"start":140577753,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140577753,"strand":1,"feature_type":"variation"},{"id":"rs1028811665","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140577754,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577754,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798365063","end":140577755,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140577755,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577766,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140577766,"clinical_significance":[],"id":"rs1453248372","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577767,"feature_type":"variation","strand":1,"end":140577767,"alleles":["C","G"],"clinical_significance":[],"id":"rs547249340","seq_region_name":"7"},{"start":140577776,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140577776,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798365617","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577781,"source":"dbSNP","strand":1,"feature_type":"variation","end":140577781,"alleles":["T","C"],"seq_region_name":"7","id":"rs1798365790","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1265235099","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577786,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140577786},{"seq_region_name":"7","id":"rs1798366161","clinical_significance":[],"start":140577787,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140577787,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577793,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GCAGCTG","GCAGCTGGCAGCTG"],"end":140577799,"seq_region_name":"7","id":"rs1798366340","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs565629168","source":"dbSNP","start":140577796,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140577796,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1354094192","end":140577807,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140577807,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140577808,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140577808,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs140714866"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1238160855","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577809,"feature_type":"variation","strand":1,"end":140577809,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs754818160","clinical_significance":[],"alleles":["G","A"],"end":140577810,"strand":1,"feature_type":"variation","start":140577810,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["A","G"],"end":140577812,"strand":1,"feature_type":"variation","start":140577812,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1269622535","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140577817,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140577817,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1275500071"},{"id":"rs1798367873","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["AA","A"],"end":140577818,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577817,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1438749719","alleles":["A","G"],"end":140577818,"feature_type":"variation","strand":1,"source":"dbSNP","start":140577818,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs891855141","clinical_significance":[],"end":140577819,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140577819,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs979364583","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140577820,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577820},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130622638","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140577822,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577822},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577824,"feature_type":"variation","strand":1,"end":140577824,"alleles":["C","T"],"clinical_significance":[],"id":"rs1798368588","seq_region_name":"7"},{"seq_region_name":"7","id":"rs557508641","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577826,"source":"dbSNP","strand":1,"feature_type":"variation","end":140577826,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798368915","feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140577827,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577827},{"id":"rs1401177467","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140577830,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577830,"source":"dbSNP"},{"id":"rs1798369367","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577832,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140577832},{"seq_region_name":"7","id":"rs1798369545","clinical_significance":[],"end":140577839,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140577839,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs2130622687","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140577847,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577847,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798369728","source":"dbSNP","start":140577851,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140577851,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1362769836","feature_type":"variation","strand":1,"end":140577852,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577852},{"seq_region_name":"7","id":"rs1032796873","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577863,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140577863},{"clinical_significance":[],"id":"rs1484721867","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","T"],"end":140577864,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577864},{"end":140577865,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140577865,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798370193","clinical_significance":[]},{"seq_region_name":"7","id":"rs1374407565","clinical_significance":[],"alleles":["C","T"],"end":140577866,"strand":1,"feature_type":"variation","start":140577866,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1417463468","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577866,"feature_type":"variation","strand":1,"end":140577867,"alleles":["CC","CCC"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs77236945","source":"dbSNP","start":140577867,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140577867,"alleles":["C","A","T"],"feature_type":"variation","strand":1},{"end":140577872,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140577872,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1024463230","clinical_significance":[]},{"seq_region_name":"7","id":"rs542668070","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577878,"source":"dbSNP","strand":1,"feature_type":"variation","end":140577878,"alleles":["T","C"]},{"end":140577880,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140577880,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1261474721","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs918013096","feature_type":"variation","strand":1,"end":140577883,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577883},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577886,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140577886,"seq_region_name":"7","id":"rs1798371221","clinical_significance":[]},{"id":"rs181100205","seq_region_name":"7","clinical_significance":[],"end":140577887,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140577887,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140577890,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140577890,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798372968"},{"feature_type":"variation","strand":1,"end":140577892,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577892,"clinical_significance":[],"id":"rs1798373144","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1214255732","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577895,"feature_type":"variation","strand":1,"end":140577895,"alleles":["T","A","C"]},{"end":140577896,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140577896,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130622834","clinical_significance":[]},{"seq_region_name":"7","id":"rs1488085150","clinical_significance":[],"end":140577897,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140577897,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140577907,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140577907,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130622850"},{"id":"rs1798373788","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577923,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140577923},{"id":"rs1798373973","seq_region_name":"7","clinical_significance":[],"start":140577925,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140577925,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1798374165","clinical_significance":[],"start":140577927,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140577927,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"end":140577928,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140577928,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798374424","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs767329028","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577932,"feature_type":"variation","strand":1,"end":140577932,"alleles":["G","A","C"]},{"end":140577936,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140577936,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1342909214","clinical_significance":[]},{"source":"dbSNP","start":140577937,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140577937,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130622901"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798374861","feature_type":"variation","strand":1,"end":140577947,"alleles":["TGTG","TG"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577944},{"seq_region_name":"7","id":"rs1798374982","clinical_significance":[],"strand":1,"feature_type":"variation","end":140577946,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577946,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1017098941","clinical_significance":[],"end":140577959,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140577959,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1219717765","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577966,"feature_type":"variation","strand":1,"end":140577966,"alleles":["C","A","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577971,"feature_type":"variation","strand":1,"end":140577971,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1798375360"},{"alleles":["C","T"],"end":140577974,"feature_type":"variation","strand":1,"source":"dbSNP","start":140577974,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798375490"},{"seq_region_name":"7","id":"rs949446189","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577980,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140577980},{"id":"rs962359840","seq_region_name":"7","clinical_significance":[],"start":140577981,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140577981,"alleles":["C","A","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs555734763","clinical_significance":[],"strand":1,"feature_type":"variation","end":140577983,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577983,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140577986,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577986,"clinical_significance":[],"seq_region_name":"7","id":"rs1798376027"},{"id":"rs1276690596","seq_region_name":"7","clinical_significance":[],"start":140577987,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140577987,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577988,"source":"dbSNP","strand":1,"feature_type":"variation","end":140577988,"alleles":["C","A","T"],"seq_region_name":"7","id":"rs972350273","clinical_significance":[]},{"source":"dbSNP","start":140577993,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140577993,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs980931558"},{"seq_region_name":"7","id":"rs1798376558","clinical_significance":[],"start":140577994,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140577994,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140577995,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140577995,"source":"dbSNP","id":"rs926781539","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798376780","feature_type":"variation","strand":1,"end":140577996,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140577996},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578000,"source":"dbSNP","strand":1,"feature_type":"variation","end":140578000,"alleles":["G","A"],"seq_region_name":"7","id":"rs1160078444","clinical_significance":[]},{"clinical_significance":[],"id":"rs1399358839","seq_region_name":"7","source":"dbSNP","start":140578001,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140578001,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs2130623054","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578002,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140578002},{"seq_region_name":"7","id":"rs1798377148","clinical_significance":[],"strand":1,"feature_type":"variation","end":140578003,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578003,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs79659279","feature_type":"variation","strand":1,"end":140578011,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578011},{"seq_region_name":"7","id":"rs1451905969","clinical_significance":[],"strand":1,"feature_type":"variation","end":140578015,"alleles":["TT","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578014,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578016,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140578016,"seq_region_name":"7","id":"rs1425774584","clinical_significance":[]},{"seq_region_name":"7","id":"rs1191206535","clinical_significance":[],"alleles":["T","C","G"],"end":140578017,"strand":1,"feature_type":"variation","start":140578017,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140578023,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578023,"source":"dbSNP","id":"rs752296335","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1048640188","seq_region_name":"7","end":140578024,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140578024,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140578033,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578033,"source":"dbSNP","id":"rs1798378111","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140578034,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578034,"source":"dbSNP","seq_region_name":"7","id":"rs1798378216","clinical_significance":[]},{"alleles":["G","T"],"end":140578041,"feature_type":"variation","strand":1,"source":"dbSNP","start":140578041,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798378335"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798378458","feature_type":"variation","strand":1,"end":140578044,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578044},{"start":140578047,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140578047,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs887318974","clinical_significance":[]},{"alleles":["G","C"],"end":140578051,"strand":1,"feature_type":"variation","start":140578051,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs940377607","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs955139576","source":"dbSNP","start":140578054,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C","T"],"end":140578054,"feature_type":"variation","strand":1},{"end":140578056,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140578056,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130623177"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798379259","feature_type":"variation","strand":1,"end":140578059,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578059},{"end":140578062,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140578062,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs541426243","seq_region_name":"7"},{"clinical_significance":[],"id":"rs269219","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578064,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140578064},{"clinical_significance":[],"id":"rs269218","seq_region_name":"7","source":"dbSNP","start":140578070,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140578070,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140578071,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578071,"source":"dbSNP","seq_region_name":"7","id":"rs942472922","clinical_significance":[]},{"id":"rs1380304741","seq_region_name":"7","clinical_significance":[],"start":140578071,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140578090,"alleles":["CCCTAATTGTATAGATCTCC","CC"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1344878808","source":"dbSNP","start":140578075,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140578076,"alleles":["AA","A"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140578078,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140578078,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1228456890"},{"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140578079,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578079,"source":"dbSNP","seq_region_name":"7","id":"rs545654403","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140578081,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578081,"clinical_significance":[],"id":"rs757765553","seq_region_name":"7"},{"start":140578082,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140578082,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1214662817","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578083,"feature_type":"variation","strand":1,"end":140578083,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1798380729"},{"clinical_significance":[],"seq_region_name":"7","id":"rs563700193","end":140578084,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140578084,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140578085,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578085,"source":"dbSNP","seq_region_name":"7","id":"rs1265715364","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578086,"feature_type":"variation","strand":1,"end":140578086,"alleles":["T","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1798381093"},{"source":"dbSNP","start":140578087,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140578087,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs796263528"},{"id":"rs1798381292","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140578088,"strand":1,"feature_type":"variation","start":140578088,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs779334407","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578090,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140578090},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578091,"feature_type":"variation","strand":1,"end":140578091,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs115891987"},{"seq_region_name":"7","id":"rs1014332122","clinical_significance":[],"alleles":["T","C"],"end":140578097,"strand":1,"feature_type":"variation","start":140578097,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs772528187","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578098,"source":"dbSNP","strand":1,"feature_type":"variation","end":140578098,"alleles":["G","C"]},{"start":140578100,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140578100,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798381897","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1480406248","source":"dbSNP","start":140578102,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140578102,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578103,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140578103,"seq_region_name":"7","id":"rs1798382015","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs865944867","alleles":["A","G"],"end":140578109,"feature_type":"variation","strand":1,"source":"dbSNP","start":140578109,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1459108397","alleles":["A","T"],"end":140578114,"feature_type":"variation","strand":1,"source":"dbSNP","start":140578114,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140578116,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140578116,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798382252"},{"seq_region_name":"7","id":"rs1256273754","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578117,"source":"dbSNP","strand":1,"feature_type":"variation","end":140578117,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1182909927","end":140578123,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140578123,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140578125,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578125,"source":"dbSNP","seq_region_name":"7","id":"rs1798382597","clinical_significance":[]},{"alleles":["C","A","T"],"end":140578126,"strand":1,"feature_type":"variation","start":140578126,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1410300642","clinical_significance":[]},{"seq_region_name":"7","id":"rs1198498202","clinical_significance":[],"strand":1,"feature_type":"variation","end":140578132,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578132,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798383036","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140578133,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578133},{"seq_region_name":"7","id":"rs1322866551","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578136,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140578136},{"seq_region_name":"7","id":"rs1798383347","clinical_significance":[],"end":140578141,"alleles":["AGAGA","AGA"],"strand":1,"feature_type":"variation","start":140578137,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578138,"source":"dbSNP","strand":1,"feature_type":"variation","end":140578138,"alleles":["G","A"],"id":"rs1798383485","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140578139,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140578138,"alleles":["-","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798383613"},{"start":140578139,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140578139,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs752555366","clinical_significance":[]},{"start":140578142,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140578142,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585675489","clinical_significance":[]},{"source":"dbSNP","start":140578143,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140578143,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs269217"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578147,"feature_type":"variation","strand":1,"end":140578147,"alleles":["A","C"],"clinical_significance":[],"id":"rs1353785525","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578149,"source":"dbSNP","strand":1,"feature_type":"variation","end":140578149,"alleles":["C","A"],"seq_region_name":"7","id":"rs1313854797","clinical_significance":[]},{"seq_region_name":"7","id":"rs1001621558","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140578150,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578150,"source":"dbSNP"},{"end":140578151,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140578151,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1426306351"},{"start":140578152,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140578152,"strand":1,"feature_type":"variation","id":"rs1328698458","seq_region_name":"7","clinical_significance":[]},{"end":140578154,"alleles":["T","A","G"],"strand":1,"feature_type":"variation","start":140578154,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798385179","clinical_significance":[]},{"seq_region_name":"7","id":"rs1441375076","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578156,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140578156},{"end":140578157,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140578157,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130623564"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130623569","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578158,"feature_type":"variation","strand":1,"end":140578158,"alleles":["C","G"]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140578162,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578162,"clinical_significance":[],"seq_region_name":"7","id":"rs1798385461"},{"end":140578163,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140578163,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1350466164","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140578164,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578164,"clinical_significance":[],"seq_region_name":"7","id":"rs1166610455"},{"seq_region_name":"7","id":"rs1585675572","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578168,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140578168},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578172,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140578172,"seq_region_name":"7","id":"rs1798385966","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578174,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140578174,"clinical_significance":[],"seq_region_name":"7","id":"rs1798386085"},{"clinical_significance":[],"seq_region_name":"7","id":"rs747174151","source":"dbSNP","start":140578176,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140578176,"alleles":["G","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1798386330","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578178,"feature_type":"variation","strand":1,"alleles":["T","-"],"end":140578178},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140578181,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578181,"clinical_significance":[],"seq_region_name":"7","id":"rs1017160970"},{"seq_region_name":"7","id":"rs1798386547","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578182,"source":"dbSNP","strand":1,"feature_type":"variation","end":140578182,"alleles":["G","C"]},{"seq_region_name":"7","id":"rs1403444899","clinical_significance":[],"strand":1,"feature_type":"variation","end":140578183,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578183,"source":"dbSNP"},{"source":"dbSNP","start":140578190,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140578190,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1798386778","seq_region_name":"7"},{"seq_region_name":"7","id":"rs984662256","clinical_significance":[],"alleles":["G","A","C"],"end":140578191,"strand":1,"feature_type":"variation","start":140578191,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1798387054","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578195,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140578195},{"seq_region_name":"7","id":"rs1441784147","clinical_significance":[],"end":140578196,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140578196,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1236370963","clinical_significance":[],"alleles":["A","G"],"end":140578199,"strand":1,"feature_type":"variation","start":140578199,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1798387421","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140578200,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578200},{"clinical_significance":[],"seq_region_name":"7","id":"rs908808158","end":140578201,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140578201,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs962917541","clinical_significance":[],"start":140578205,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140578205,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1249012912","seq_region_name":"7","source":"dbSNP","start":140578208,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140578208,"alleles":["G","T"],"feature_type":"variation","strand":1},{"start":140578212,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140578212,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs1219798382","seq_region_name":"7","clinical_significance":[]},{"end":140578214,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140578214,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798388004","clinical_significance":[]},{"seq_region_name":"7","id":"rs768769799","clinical_significance":[],"strand":1,"feature_type":"variation","end":140578215,"alleles":["G","C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578215,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578223,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140578223,"clinical_significance":[],"seq_region_name":"7","id":"rs994269490"},{"end":140578224,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140578224,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1025303164","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs955340145","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578226,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140578226},{"end":140578227,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140578227,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs576039002","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798388671","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578227,"feature_type":"variation","strand":1,"alleles":["GGGG","GGGGG"],"end":140578230},{"id":"rs1798388775","seq_region_name":"7","clinical_significance":[],"end":140578229,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140578229,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1798388898","clinical_significance":[],"strand":1,"feature_type":"variation","end":140578230,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578230,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585675702","source":"dbSNP","start":140578231,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140578231,"alleles":["T","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1798389156","seq_region_name":"7","feature_type":"variation","strand":1,"end":140578232,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578232},{"seq_region_name":"7","id":"rs1050175150","clinical_significance":[],"strand":1,"feature_type":"variation","end":140578237,"alleles":["GGGGGG","GGGGGGG"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578232,"source":"dbSNP"},{"alleles":["G","T"],"end":140578233,"strand":1,"feature_type":"variation","start":140578233,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798389423","clinical_significance":[]},{"alleles":["G","A","C"],"end":140578237,"strand":1,"feature_type":"variation","start":140578237,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs561734526","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs888826252","clinical_significance":[],"strand":1,"feature_type":"variation","end":140578238,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578238,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140578241,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578241,"clinical_significance":[],"seq_region_name":"7","id":"rs2130623847"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578244,"source":"dbSNP","strand":1,"feature_type":"variation","end":140578244,"alleles":["G","A"],"seq_region_name":"7","id":"rs1295166486","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578245,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140578245,"id":"rs1563154377","seq_region_name":"7","clinical_significance":[]},{"end":140578247,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140578247,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1312982747"},{"alleles":["G","A"],"end":140578250,"strand":1,"feature_type":"variation","start":140578250,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs986570991","seq_region_name":"7","clinical_significance":[]},{"start":140578253,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140578253,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798390261","clinical_significance":[]},{"alleles":["G","A"],"end":140578256,"feature_type":"variation","strand":1,"source":"dbSNP","start":140578256,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798390401"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140578259,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578259,"clinical_significance":[],"seq_region_name":"7","id":"rs1323205813"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798390645","end":140578261,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140578261,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140578261,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140578264,"alleles":["CCCC","CCCCC"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1364658972","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140578262,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578262,"source":"dbSNP","id":"rs1248554500","seq_region_name":"7","clinical_significance":[]},{"id":"rs1421739635","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578263,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140578263},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140578273,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578273,"source":"dbSNP","seq_region_name":"7","id":"rs910940311","clinical_significance":[]},{"source":"dbSNP","start":140578274,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140578274,"alleles":["G","C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs963886905","seq_region_name":"7"},{"end":140578281,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140578281,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1490318998"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578283,"feature_type":"variation","strand":1,"end":140578283,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs11982424"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1189914903","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140578288,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578288},{"start":140578289,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140578289,"strand":1,"feature_type":"variation","id":"rs1009427886","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798392541","source":"dbSNP","start":140578293,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140578293,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578300,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140578300,"seq_region_name":"7","id":"rs1798392673","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140578302,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578302,"clinical_significance":[],"seq_region_name":"7","id":"rs1798392796"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578305,"feature_type":"variation","strand":1,"end":140578305,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1264326211"},{"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140578306,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578306,"source":"dbSNP","seq_region_name":"7","id":"rs1219333692","clinical_significance":[]},{"id":"rs1489048521","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140578307,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578307,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140578313,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578313,"source":"dbSNP","id":"rs925214460","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798393493","feature_type":"variation","strand":1,"end":140578320,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578320},{"source":"dbSNP","start":140578323,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140578323,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs796975134"},{"source":"dbSNP","start":140578324,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140578324,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs935221850"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578328,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140578328,"seq_region_name":"7","id":"rs989251003","clinical_significance":[]},{"alleles":["T","A"],"end":140578330,"feature_type":"variation","strand":1,"source":"dbSNP","start":140578330,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798393857"},{"seq_region_name":"7","id":"rs1217349803","clinical_significance":[],"start":140578331,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140578331,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798394059","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578332,"feature_type":"variation","strand":1,"end":140578332,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1585675967","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578333,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140578333},{"clinical_significance":[],"seq_region_name":"7","id":"rs1344869007","end":140578335,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140578335,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs913228188","seq_region_name":"7","clinical_significance":[],"alleles":["C","G"],"end":140578338,"strand":1,"feature_type":"variation","start":140578338,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1401661845","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140578340,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578340,"source":"dbSNP"},{"id":"rs1798394643","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578344,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140578344},{"clinical_significance":[],"id":"rs1798394794","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140578347,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578347},{"source":"dbSNP","start":140578353,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140578353,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798394898"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1358838580","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578358,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140578358},{"clinical_significance":[],"id":"rs2130624177","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578361,"feature_type":"variation","strand":1,"end":140578361,"alleles":["C","G"]},{"strand":1,"feature_type":"variation","end":140578362,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578362,"source":"dbSNP","seq_region_name":"7","id":"rs1288462500","clinical_significance":[]},{"end":140578366,"alleles":["G","C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140578366,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1798395184","seq_region_name":"7"},{"end":140578368,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140578368,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1466747048","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798395431","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140578372,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578372,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140578374,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578374,"clinical_significance":[],"seq_region_name":"7","id":"rs1798395543"},{"start":140578375,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140578375,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130624220","clinical_significance":[]},{"seq_region_name":"7","id":"rs546986560","clinical_significance":[],"strand":1,"feature_type":"variation","end":140578377,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578377,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1798395795","clinical_significance":[],"alleles":["CTCT","CT"],"end":140578389,"strand":1,"feature_type":"variation","start":140578386,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1360905029","seq_region_name":"7","clinical_significance":[],"end":140578388,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140578388,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["T","A"],"end":140578389,"feature_type":"variation","strand":1,"source":"dbSNP","start":140578389,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585676045"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578393,"feature_type":"variation","strand":1,"end":140578393,"alleles":["T","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1798396145"},{"id":"rs1563154466","seq_region_name":"7","clinical_significance":[],"start":140578394,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140578394,"alleles":["G","-"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1798396367","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140578396,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578396},{"end":140578398,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140578398,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1174114874","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1798396573","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578399,"feature_type":"variation","strand":1,"end":140578399,"alleles":["A","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798396690","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578405,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140578405},{"start":140578407,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140578407,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs950052196","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578408,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140578408,"clinical_significance":[],"seq_region_name":"7","id":"rs1002123669"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578409,"feature_type":"variation","strand":1,"end":140578409,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1446685993"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1161364188","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578416,"feature_type":"variation","strand":1,"end":140578416,"alleles":["G","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578418,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140578418,"seq_region_name":"7","id":"rs1477017343","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578421,"feature_type":"variation","strand":1,"end":140578421,"alleles":["A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130624332"},{"strand":1,"feature_type":"variation","end":140578428,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578428,"source":"dbSNP","id":"rs1798397413","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140578429,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140578429,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1033777110","seq_region_name":"7"},{"id":"rs1798397646","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140578432,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578432,"source":"dbSNP"},{"end":140578433,"alleles":["T","-"],"strand":1,"feature_type":"variation","start":140578433,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1185510140","clinical_significance":[]},{"id":"rs866958562","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578435,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140578435},{"clinical_significance":[],"id":"rs1798397967","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578436,"feature_type":"variation","strand":1,"end":140578436,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1257231926","clinical_significance":[],"strand":1,"feature_type":"variation","end":140578437,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578437,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140578438,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578438,"source":"dbSNP","id":"rs1430224223","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140578444,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578444,"source":"dbSNP","seq_region_name":"7","id":"rs1585676156","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578450,"feature_type":"variation","strand":1,"end":140578450,"alleles":["A","C"],"clinical_significance":[],"id":"rs1798398410","seq_region_name":"7"},{"end":140578452,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140578452,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1322697102","seq_region_name":"7"},{"end":140578453,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140578453,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1798398614","seq_region_name":"7"},{"id":"rs1258693137","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140578455,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578455,"source":"dbSNP"},{"id":"rs1798398824","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578456,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140578456},{"seq_region_name":"7","id":"rs1798398944","clinical_significance":[],"start":140578457,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140578457,"alleles":["T","G"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578463,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140578463,"clinical_significance":[],"id":"rs1330776071","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578464,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140578464,"id":"rs1352759760","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","C"],"end":140578467,"feature_type":"variation","strand":1,"source":"dbSNP","start":140578467,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs984325125"},{"alleles":["A","T"],"end":140578468,"feature_type":"variation","strand":1,"source":"dbSNP","start":140578468,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798399436"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578472,"source":"dbSNP","strand":1,"feature_type":"variation","end":140578472,"alleles":["G","C"],"seq_region_name":"7","id":"rs1294596976","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140578473,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578473,"clinical_significance":[],"id":"rs1798399668","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578474,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140578474,"seq_region_name":"7","id":"rs905925791","clinical_significance":[]},{"id":"rs144537246","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578476,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140578476},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798400096","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140578477,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578477},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130624547","alleles":["C","T"],"end":140578478,"feature_type":"variation","strand":1,"source":"dbSNP","start":140578478,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140578483,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140578483,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs746932935"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578483,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CTGTCTGTC","CTGTC"],"end":140578491,"id":"rs908686466","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140578485,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578485,"clinical_significance":[],"seq_region_name":"7","id":"rs1798400448"},{"seq_region_name":"7","id":"rs1798400540","clinical_significance":[],"start":140578492,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140578492,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["ACAAACA","ACA"],"end":140578504,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578498,"source":"dbSNP","seq_region_name":"7","id":"rs1798400656","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578499,"source":"dbSNP","strand":1,"feature_type":"variation","end":140578499,"alleles":["C","A","G","T"],"seq_region_name":"7","id":"rs184058720","clinical_significance":[]},{"clinical_significance":[],"id":"rs1798400910","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578502,"feature_type":"variation","strand":1,"end":140578508,"alleles":["ACATACA","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798401013","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578503,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140578503},{"seq_region_name":"7","id":"rs976997659","clinical_significance":[],"strand":1,"feature_type":"variation","end":140578508,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578508,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578510,"source":"dbSNP","strand":1,"feature_type":"variation","end":140578510,"alleles":["A","G"],"seq_region_name":"7","id":"rs1798401251","clinical_significance":[]},{"alleles":["T","A"],"end":140578512,"feature_type":"variation","strand":1,"source":"dbSNP","start":140578512,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1359141098"},{"clinical_significance":[],"seq_region_name":"7","id":"rs539313396","alleles":["C","A","T"],"end":140578515,"feature_type":"variation","strand":1,"source":"dbSNP","start":140578515,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140578519,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578519,"source":"dbSNP","seq_region_name":"7","id":"rs1229652595","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140578520,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578520,"source":"dbSNP","seq_region_name":"7","id":"rs551183134","clinical_significance":[]},{"seq_region_name":"7","id":"rs922807617","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578521,"source":"dbSNP","strand":1,"feature_type":"variation","end":140578521,"alleles":["T","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798401922","source":"dbSNP","start":140578522,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140578522,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1424025865","clinical_significance":[],"end":140578524,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140578524,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1798402142","clinical_significance":[],"end":140578526,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140578526,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140578529,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140578529,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1275711476","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578530,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140578530,"clinical_significance":[],"seq_region_name":"7","id":"rs932980951"},{"strand":1,"feature_type":"variation","end":140578534,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578534,"source":"dbSNP","seq_region_name":"7","id":"rs1798402486","clinical_significance":[]},{"source":"dbSNP","start":140578535,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140578535,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs898786931"},{"start":140578536,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140578536,"alleles":["A","C"],"strand":1,"feature_type":"variation","id":"rs569701612","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1238292663","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578539,"source":"dbSNP","strand":1,"feature_type":"variation","end":140578539,"alleles":["C","T"]},{"source":"dbSNP","start":140578543,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140578543,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1200393266"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1337432573","alleles":["G","A","C"],"end":140578546,"feature_type":"variation","strand":1,"source":"dbSNP","start":140578546,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs994429182","source":"dbSNP","start":140578547,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140578547,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140578549,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140578549,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1245290435"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578551,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AAAAAA","AAAAAAA"],"end":140578556,"id":"rs1798403384","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140578556,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140578556,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1798403503","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578556,"feature_type":"variation","strand":1,"alleles":["AGAGA","AGA"],"end":140578560,"clinical_significance":[],"seq_region_name":"7","id":"rs1323706805"},{"source":"dbSNP","start":140578561,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140578561,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1313127432"},{"alleles":["T","C","G"],"end":140578564,"strand":1,"feature_type":"variation","start":140578564,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1306323521","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140578565,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578565,"source":"dbSNP","seq_region_name":"7","id":"rs146659860","clinical_significance":[]},{"source":"dbSNP","start":140578575,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C","G"],"end":140578575,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1333462547","seq_region_name":"7"},{"seq_region_name":"7","id":"rs890806791","clinical_significance":[],"strand":1,"feature_type":"variation","end":140578585,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578585,"source":"dbSNP"},{"end":140578591,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140578591,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1445199646","seq_region_name":"7"},{"start":140578593,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140578593,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs189835315","clinical_significance":[]},{"clinical_significance":[],"id":"rs1164168872","seq_region_name":"7","alleles":["G","A"],"end":140578598,"feature_type":"variation","strand":1,"source":"dbSNP","start":140578598,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140578600,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140578600,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1459816587"},{"clinical_significance":[],"seq_region_name":"7","id":"rs76062806","source":"dbSNP","start":140578601,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140578601,"alleles":["C","T"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140578602,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578602,"clinical_significance":[],"id":"rs948050358","seq_region_name":"7"},{"start":140578605,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140578605,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1462791442","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578609,"source":"dbSNP","strand":1,"feature_type":"variation","end":140578609,"alleles":["A","G"],"id":"rs1798405144","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578614,"feature_type":"variation","strand":1,"end":140578614,"alleles":["C","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1053656026"},{"id":"rs1798405353","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578616,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140578616},{"clinical_significance":[],"seq_region_name":"7","id":"rs761858443","source":"dbSNP","start":140578618,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","G","T"],"end":140578618,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578619,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140578619,"clinical_significance":[],"id":"rs892287464","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578623,"feature_type":"variation","strand":1,"end":140578623,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs879451745"},{"seq_region_name":"7","id":"rs1210382697","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140578629,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578629,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140578630,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578630,"clinical_significance":[],"seq_region_name":"7","id":"rs1563154647"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578632,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140578632,"id":"rs1798406124","seq_region_name":"7","clinical_significance":[]},{"id":"rs1585676652","seq_region_name":"7","clinical_significance":[],"end":140578634,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140578634,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578635,"source":"dbSNP","strand":1,"feature_type":"variation","end":140578635,"alleles":["C","T"],"seq_region_name":"7","id":"rs1798406321","clinical_significance":[]},{"end":140578636,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140578636,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1018054555"},{"start":140578638,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140578638,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798406567","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798406669","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140578644,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578644,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140578651,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578651,"source":"dbSNP","id":"rs963771645","seq_region_name":"7","clinical_significance":[]},{"start":140578652,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140578652,"strand":1,"feature_type":"variation","id":"rs373860244","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1038764244","clinical_significance":[],"alleles":["T","G"],"end":140578655,"strand":1,"feature_type":"variation","start":140578655,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["G","A"],"end":140578656,"feature_type":"variation","strand":1,"source":"dbSNP","start":140578656,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1798407121","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578658,"source":"dbSNP","strand":1,"feature_type":"variation","end":140578658,"alleles":["A","T"],"seq_region_name":"7","id":"rs1798407236","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1245450092","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140578670,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578670},{"strand":1,"feature_type":"variation","end":140578673,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578673,"source":"dbSNP","id":"rs1354764766","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1032168482","clinical_significance":[],"strand":1,"feature_type":"variation","end":140578676,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578676,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578678,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140578678,"seq_region_name":"7","id":"rs181939662","clinical_significance":[]},{"seq_region_name":"7","id":"rs1237027325","clinical_significance":[],"start":140578679,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140578679,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140578682,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578682,"clinical_significance":[],"seq_region_name":"7","id":"rs988077202"},{"seq_region_name":"7","id":"rs368345086","clinical_significance":[],"alleles":["T","C"],"end":140578689,"strand":1,"feature_type":"variation","start":140578689,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs553385252","clinical_significance":[],"start":140578696,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","G"],"end":140578696,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1324734767","source":"dbSNP","start":140578697,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140578697,"alleles":["A","G"],"feature_type":"variation","strand":1},{"alleles":["C","T"],"end":140578698,"feature_type":"variation","strand":1,"source":"dbSNP","start":140578698,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs917791528","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578699,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140578699,"clinical_significance":[],"id":"rs950091443","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140578700,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578700,"source":"dbSNP","id":"rs1798408581","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140578701,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140578701,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798408693"},{"end":140578702,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140578702,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798408795"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1335633791","end":140578709,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140578709,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1365553869","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578710,"source":"dbSNP","strand":1,"feature_type":"variation","end":140578710,"alleles":["G","A"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578718,"feature_type":"variation","strand":1,"end":140578718,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1302981950"},{"strand":1,"feature_type":"variation","end":140578724,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578724,"source":"dbSNP","seq_region_name":"7","id":"rs2130625179","clinical_significance":[]},{"id":"rs1798409233","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140578726,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578726,"source":"dbSNP"},{"start":140578728,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140578728,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798409332","clinical_significance":[]},{"source":"dbSNP","start":140578729,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140578729,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798409446"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798409551","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578738,"feature_type":"variation","strand":1,"end":140578738,"alleles":["G","C"]},{"clinical_significance":[],"id":"rs1431909238","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140578739,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578739},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140578741,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578741,"source":"dbSNP","id":"rs1798409787","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs981391742","feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140578745,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578745},{"id":"rs2130625260","seq_region_name":"7","clinical_significance":[],"alleles":["A","G"],"end":140578747,"strand":1,"feature_type":"variation","start":140578747,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140578749,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C","G"],"end":140578749,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1009478885"},{"alleles":["G","A"],"end":140578751,"strand":1,"feature_type":"variation","start":140578751,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798410164","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1360408108","alleles":["G","A"],"end":140578752,"feature_type":"variation","strand":1,"source":"dbSNP","start":140578752,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140578754,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578754,"source":"dbSNP","id":"rs1046301650","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","A"],"end":140578755,"feature_type":"variation","strand":1,"source":"dbSNP","start":140578755,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798410488"},{"clinical_significance":[],"seq_region_name":"7","id":"rs906428534","end":140578757,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140578757,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1307703385","clinical_significance":[],"alleles":["C","A","T"],"end":140578759,"strand":1,"feature_type":"variation","start":140578759,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140578760,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140578760,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","id":"rs1214532139","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798411357","clinical_significance":[],"end":140578766,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140578766,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140578769,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140578769,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1434851441"},{"end":140578772,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140578772,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1263778756","clinical_significance":[]},{"end":140578778,"alleles":["A","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140578778,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs578254622"},{"strand":1,"feature_type":"variation","end":140578780,"alleles":["A","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578780,"source":"dbSNP","id":"rs370882115","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs545691372","clinical_significance":[],"alleles":["G","A"],"end":140578781,"strand":1,"feature_type":"variation","start":140578781,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["GG","-"],"end":140578782,"feature_type":"variation","strand":1,"source":"dbSNP","start":140578781,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs145249385"},{"alleles":["G","A"],"end":140578784,"strand":1,"feature_type":"variation","start":140578784,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798412235","clinical_significance":[]},{"start":140578784,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140578787,"alleles":["GAAT","GAATGAAT"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1350001199","clinical_significance":[]},{"id":"rs564737028","seq_region_name":"7","clinical_significance":[],"start":140578788,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","T"],"end":140578788,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1262736830","clinical_significance":[],"start":140578789,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140578789,"alleles":["G","A","T"],"strand":1,"feature_type":"variation"},{"start":140578793,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140578793,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798412790","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578794,"source":"dbSNP","strand":1,"feature_type":"variation","end":140578794,"alleles":["A","T"],"id":"rs1344240968","seq_region_name":"7","clinical_significance":[]},{"id":"rs141494392","seq_region_name":"7","clinical_significance":[],"start":140578795,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140578795,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs770881652","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578797,"feature_type":"variation","strand":1,"end":140578797,"alleles":["C","A"]},{"seq_region_name":"7","id":"rs1798413242","clinical_significance":[],"start":140578798,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140578798,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"start":140578799,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140578799,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798413331","clinical_significance":[]},{"seq_region_name":"7","id":"rs187147266","clinical_significance":[],"end":140578800,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140578800,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs575710943","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140578804,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578804},{"start":140578805,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140578805,"strand":1,"feature_type":"variation","id":"rs139978690","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs2130625525","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140578814,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578814},{"source":"dbSNP","start":140578821,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140578821,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798413841"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578822,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140578822,"id":"rs1798413961","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578829,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140578829,"seq_region_name":"7","id":"rs898670936","clinical_significance":[]},{"alleles":["AT","-"],"end":140578830,"strand":1,"feature_type":"variation","start":140578829,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1194984667","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140578830,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578830,"clinical_significance":[],"id":"rs1240178549","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1383539587","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578831,"source":"dbSNP","strand":1,"feature_type":"variation","end":140578831,"alleles":["G","A"]},{"feature_type":"variation","strand":1,"alleles":["C","CAC"],"end":140578832,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578832,"clinical_significance":[],"id":"rs1475016619","seq_region_name":"7"},{"id":"rs543197261","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578835,"source":"dbSNP","strand":1,"feature_type":"variation","end":140578835,"alleles":["C","T"]},{"source":"dbSNP","start":140578836,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140578836,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798414822"},{"seq_region_name":"7","id":"rs1015801248","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578838,"source":"dbSNP","strand":1,"feature_type":"variation","end":140578838,"alleles":["C","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578840,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140578840,"seq_region_name":"7","id":"rs1431405205","clinical_significance":[]},{"source":"dbSNP","start":140578842,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140578842,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798415174"},{"clinical_significance":[],"seq_region_name":"7","id":"rs868213952","feature_type":"variation","strand":1,"end":140578843,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578843},{"source":"dbSNP","start":140578847,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140578847,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs112329407"},{"id":"rs192434440","seq_region_name":"7","clinical_significance":[],"start":140578852,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140578852,"alleles":["C","A","T"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140578853,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140578853,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1191220406"},{"end":140578858,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140578858,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs891349688","clinical_significance":[]},{"source":"dbSNP","start":140578859,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140578859,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs10255623"},{"feature_type":"variation","strand":1,"end":140578860,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578860,"clinical_significance":[],"seq_region_name":"7","id":"rs2130625675"},{"clinical_significance":[],"id":"rs558895312","seq_region_name":"7","source":"dbSNP","start":140578865,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140578865,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs899617985","alleles":["T","A","C"],"end":140578866,"feature_type":"variation","strand":1,"source":"dbSNP","start":140578866,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1000614114","seq_region_name":"7","alleles":["C","G","T"],"end":140578868,"feature_type":"variation","strand":1,"source":"dbSNP","start":140578868,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140578869,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140578869,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1219814729","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578871,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140578871,"clinical_significance":[],"seq_region_name":"7","id":"rs533061173"},{"end":140578878,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140578878,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1798416545","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130625744","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140578881,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578881},{"id":"rs1268799344","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578886,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140578886},{"clinical_significance":[],"id":"rs936469589","seq_region_name":"7","end":140578891,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140578891,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1325560508","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578892,"source":"dbSNP","strand":1,"feature_type":"variation","end":140578897,"alleles":["AGAAAG","AG"]},{"seq_region_name":"7","id":"rs1334215352","clinical_significance":[],"end":140578895,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140578895,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798417089","alleles":["C","T"],"end":140578899,"feature_type":"variation","strand":1,"source":"dbSNP","start":140578899,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140578900,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TT","T"],"end":140578901,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1470698645","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1403296426","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140578901,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578901},{"clinical_significance":[],"id":"rs956572393","seq_region_name":"7","feature_type":"variation","strand":1,"end":140578902,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578902},{"alleles":["C","T"],"end":140578903,"strand":1,"feature_type":"variation","start":140578903,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130625806","clinical_significance":[]},{"seq_region_name":"7","id":"rs142584572","clinical_significance":[],"start":140578904,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140578904,"alleles":["A","C","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1421317840","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140578907,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578907},{"start":140578908,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140578908,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798417810","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798417911","clinical_significance":[],"strand":1,"feature_type":"variation","end":140578910,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578910,"source":"dbSNP"},{"clinical_significance":[],"id":"rs569923654","seq_region_name":"7","alleles":["T","G"],"end":140578920,"feature_type":"variation","strand":1,"source":"dbSNP","start":140578920,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs945219248","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578921,"source":"dbSNP","strand":1,"feature_type":"variation","end":140578921,"alleles":["G","A"]},{"id":"rs1798418254","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578923,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140578923},{"start":140578924,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140578924,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1238315367","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798418488","clinical_significance":[],"alleles":["A","T"],"end":140578925,"strand":1,"feature_type":"variation","start":140578925,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140578939,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578939,"source":"dbSNP","seq_region_name":"7","id":"rs185193114","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140578942,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578942,"source":"dbSNP","seq_region_name":"7","id":"rs1798418724","clinical_significance":[]},{"seq_region_name":"7","id":"rs981444039","clinical_significance":[],"alleles":["T","G"],"end":140578949,"strand":1,"feature_type":"variation","start":140578949,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1460004470","clinical_significance":[],"end":140578957,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140578957,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs269216","feature_type":"variation","strand":1,"end":140578958,"alleles":["G","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578958},{"seq_region_name":"7","id":"rs1320690321","clinical_significance":[],"end":140578960,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140578960,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140578964,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140578964,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1271319474"},{"clinical_significance":[],"seq_region_name":"7","id":"rs753364947","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578965,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140578965},{"clinical_significance":[],"id":"rs1214391248","seq_region_name":"7","source":"dbSNP","start":140578965,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","-"],"end":140578965,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130625947","alleles":["A","C"],"end":140578966,"feature_type":"variation","strand":1,"source":"dbSNP","start":140578966,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140578968,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578968,"source":"dbSNP","seq_region_name":"7","id":"rs1798419789","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798419904","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140578969,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578969},{"seq_region_name":"7","id":"rs1338321760","clinical_significance":[],"strand":1,"feature_type":"variation","end":140578975,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578975,"source":"dbSNP"},{"start":140578976,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140578976,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798420133","clinical_significance":[]},{"seq_region_name":"7","id":"rs974136620","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578979,"source":"dbSNP","strand":1,"feature_type":"variation","end":140578979,"alleles":["T","C","G"]},{"start":140578987,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140578987,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1222114061","clinical_significance":[]},{"start":140578989,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140578989,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1379860168","clinical_significance":[]},{"seq_region_name":"7","id":"rs1211113521","clinical_significance":[],"strand":1,"feature_type":"variation","end":140579012,"alleles":["AATTAGGCTAGATGCGGTGGCTCA","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578989,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140578992,"feature_type":"variation","strand":1,"end":140578992,"alleles":["T","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1798420708"},{"source":"dbSNP","start":140578994,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140578994,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs11767590"},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140578999,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140578999,"source":"dbSNP","seq_region_name":"7","id":"rs919977470","clinical_significance":[]},{"alleles":["C","T"],"end":140579003,"strand":1,"feature_type":"variation","start":140579003,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs937909123","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140579004,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579004,"source":"dbSNP","id":"rs1798421182","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1447413352","clinical_significance":[],"start":140579007,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140579007,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs930179361","clinical_significance":[],"alleles":["C","T"],"end":140579011,"strand":1,"feature_type":"variation","start":140579011,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140579011,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140579011,"alleles":["C","-"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798421515","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140579016,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579016,"clinical_significance":[],"seq_region_name":"7","id":"rs1270939007"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579017,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140579017,"clinical_significance":[],"seq_region_name":"7","id":"rs1798421743"},{"feature_type":"variation","strand":1,"end":140579023,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579023,"clinical_significance":[],"id":"rs1356245764","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140579024,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579024,"source":"dbSNP","seq_region_name":"7","id":"rs1047657223","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798422095","clinical_significance":[],"alleles":["T","G"],"end":140579026,"strand":1,"feature_type":"variation","start":140579026,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140579027,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140579027,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs371717101","seq_region_name":"7"},{"alleles":["C","A","T"],"end":140579029,"feature_type":"variation","strand":1,"source":"dbSNP","start":140579029,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs548410543"},{"feature_type":"variation","strand":1,"end":140579030,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579030,"clinical_significance":[],"seq_region_name":"7","id":"rs1798422467"},{"start":140579032,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140579032,"alleles":["A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798422600","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579034,"feature_type":"variation","strand":1,"end":140579034,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1798422707"},{"seq_region_name":"7","id":"rs1414294239","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579035,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140579035},{"seq_region_name":"7","id":"rs866762314","clinical_significance":[],"start":140579036,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140579036,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579038,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140579038,"seq_region_name":"7","id":"rs1443022539","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140579043,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579043,"source":"dbSNP","id":"rs1798423176","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579044,"feature_type":"variation","strand":1,"end":140579044,"alleles":["C","A"],"clinical_significance":[],"id":"rs1798423282","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579046,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140579046,"seq_region_name":"7","id":"rs944280231","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798423510","feature_type":"variation","strand":1,"end":140579047,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579047},{"clinical_significance":[],"seq_region_name":"7","id":"rs113547216","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140579048,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579048},{"start":140579051,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TTT","TTTT"],"end":140579053,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs34390380","clinical_significance":[]},{"id":"rs897215182","seq_region_name":"7","clinical_significance":[],"start":140579056,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140579056,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"start":140579059,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140579059,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1470930329","clinical_significance":[]},{"id":"rs1798423957","seq_region_name":"7","clinical_significance":[],"start":140579063,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140579063,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140579064,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579064,"clinical_significance":[],"seq_region_name":"7","id":"rs1156423810"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579065,"feature_type":"variation","strand":1,"end":140579065,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1798424191"},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140579068,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579068,"clinical_significance":[],"seq_region_name":"7","id":"rs1798424306"},{"clinical_significance":[],"id":"rs899500320","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579070,"feature_type":"variation","strand":1,"end":140579070,"alleles":["C","A","G","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579071,"source":"dbSNP","strand":1,"feature_type":"variation","end":140579071,"alleles":["G","A"],"seq_region_name":"7","id":"rs570168423","clinical_significance":[]},{"source":"dbSNP","start":140579074,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140579074,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1400480369"},{"end":140579077,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140579077,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs2130626298","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579080,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140579080,"clinical_significance":[],"seq_region_name":"7","id":"rs1292478973"},{"seq_region_name":"7","id":"rs1029816828","clinical_significance":[],"strand":1,"feature_type":"variation","end":140579081,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579081,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579082,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140579082,"seq_region_name":"7","id":"rs1367933992","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1403675792","feature_type":"variation","strand":1,"alleles":["AA","-"],"end":140579085,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579084},{"start":140579091,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G","T"],"end":140579091,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1302580038","clinical_significance":[]},{"alleles":["G","A"],"end":140579092,"strand":1,"feature_type":"variation","start":140579092,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1374902819","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1277657352","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579093,"source":"dbSNP","strand":1,"feature_type":"variation","end":140579093,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1441393750","source":"dbSNP","start":140579096,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["CC","C"],"end":140579097,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579097,"source":"dbSNP","strand":1,"feature_type":"variation","end":140579097,"alleles":["C","T"],"seq_region_name":"7","id":"rs1798425801","clinical_significance":[]},{"alleles":["A","G"],"end":140579098,"strand":1,"feature_type":"variation","start":140579098,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1798425904","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798426028","clinical_significance":[],"alleles":["T","C","G"],"end":140579099,"strand":1,"feature_type":"variation","start":140579099,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1798426192","clinical_significance":[],"end":140579100,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140579100,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140579101,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140579101,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1336404971","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140579105,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579105,"clinical_significance":[],"seq_region_name":"7","id":"rs2130626400"},{"seq_region_name":"7","id":"rs954305648","clinical_significance":[],"strand":1,"feature_type":"variation","end":140579106,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579106,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579109,"feature_type":"variation","strand":1,"end":140579109,"alleles":["A","G"],"clinical_significance":[],"id":"rs1422970916","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1365231728","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579110,"feature_type":"variation","strand":1,"end":140579110,"alleles":["T","A","C"]},{"clinical_significance":[],"id":"rs1053544502","seq_region_name":"7","end":140579113,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140579113,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585677827","alleles":["A","G"],"end":140579117,"feature_type":"variation","strand":1,"source":"dbSNP","start":140579117,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1798427141","clinical_significance":[],"start":140579118,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140579118,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1798427329","clinical_significance":[],"start":140579119,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140579119,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579120,"source":"dbSNP","strand":1,"feature_type":"variation","end":140579120,"alleles":["C","T"],"seq_region_name":"7","id":"rs1277996616","clinical_significance":[]},{"start":140579122,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140579122,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1420909626","clinical_significance":[]},{"end":140579123,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","start":140579123,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs986110041","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs892184531","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579142,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140579142},{"id":"rs1478652196","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140579143,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579143,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1271484722","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579144,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140579144},{"id":"rs1246360300","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579147,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140579147},{"id":"rs1489705316","seq_region_name":"7","clinical_significance":[],"start":140579148,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140579148,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140579152,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579152,"clinical_significance":[],"seq_region_name":"7","id":"rs1293673991"},{"id":"rs1017310980","seq_region_name":"7","clinical_significance":[],"start":140579153,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140579153,"alleles":["C","A","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798429371","feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140579154,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579154},{"seq_region_name":"7","id":"rs1798429571","clinical_significance":[],"end":140579155,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140579155,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579157,"feature_type":"variation","strand":1,"end":140579157,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130626559"},{"end":140579159,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140579159,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1009433643","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579161,"source":"dbSNP","strand":1,"feature_type":"variation","end":140579161,"alleles":["C","G","T"],"seq_region_name":"7","id":"rs1318127432","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1025222711","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140579162,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579162},{"source":"dbSNP","start":140579165,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140579165,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs970712297"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1284926179","feature_type":"variation","strand":1,"end":140579166,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579166},{"feature_type":"variation","strand":1,"end":140579167,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579167,"clinical_significance":[],"seq_region_name":"7","id":"rs1251215323"},{"seq_region_name":"7","id":"rs1798430868","clinical_significance":[],"end":140579168,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140579168,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140579173,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579173,"clinical_significance":[],"seq_region_name":"7","id":"rs1402924832"},{"source":"dbSNP","start":140579178,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140579178,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1798431214","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140579185,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579185,"source":"dbSNP","seq_region_name":"7","id":"rs1344661923","clinical_significance":[]},{"source":"dbSNP","start":140579186,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140579186,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1298991111"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579188,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140579188,"clinical_significance":[],"seq_region_name":"7","id":"rs2130626643"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579197,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140579197,"seq_region_name":"7","id":"rs1798431795","clinical_significance":[]},{"source":"dbSNP","start":140579198,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140579198,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1455545305"},{"alleles":["G","A"],"end":140579201,"feature_type":"variation","strand":1,"source":"dbSNP","start":140579201,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1439011089"},{"end":140579207,"alleles":["T","C","G"],"strand":1,"feature_type":"variation","start":140579207,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1179123245","clinical_significance":[]},{"seq_region_name":"7","id":"rs368416612","clinical_significance":[],"alleles":["C","T"],"end":140579209,"strand":1,"feature_type":"variation","start":140579209,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1472925042","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579210,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140579210},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798432897","alleles":["C","G"],"end":140579216,"feature_type":"variation","strand":1,"source":"dbSNP","start":140579216,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs989126491","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140579218,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579218,"source":"dbSNP"},{"start":140579219,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140579219,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs569722719","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140579220,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579220,"source":"dbSNP","id":"rs1033524131","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798433659","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140579222,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579222,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140579224,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579224,"source":"dbSNP","id":"rs1423189517","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1163474789","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140579225,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579225},{"clinical_significance":[],"seq_region_name":"7","id":"rs958712667","feature_type":"variation","strand":1,"end":140579226,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579226},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140579227,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579227,"clinical_significance":[],"seq_region_name":"7","id":"rs1798434348"},{"seq_region_name":"7","id":"rs1480289209","clinical_significance":[],"start":140579228,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140579228,"strand":1,"feature_type":"variation"},{"end":140579232,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140579232,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs974022234","clinical_significance":[]},{"source":"dbSNP","start":140579236,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140579236,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798434684"},{"seq_region_name":"7","id":"rs2130626795","clinical_significance":[],"end":140579237,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140579237,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1397912158","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579239,"source":"dbSNP","strand":1,"feature_type":"variation","end":140579239,"alleles":["G","A"]},{"id":"rs2130626817","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140579240,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579240,"source":"dbSNP"},{"seq_region_name":"7","id":"rs2130626824","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579242,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140579242},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140579243,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579243,"clinical_significance":[],"id":"rs1798434901","seq_region_name":"7"},{"seq_region_name":"7","id":"rs553759965","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579244,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GATTGTG","GATTGTGATTGTG"],"end":140579250},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798435100","end":140579246,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140579246,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140579247,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140579247,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130626863","clinical_significance":[]},{"clinical_significance":[],"id":"rs1486674846","seq_region_name":"7","end":140579257,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140579257,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140579259,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579259,"source":"dbSNP","id":"rs1798435287","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579261,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140579261,"seq_region_name":"7","id":"rs1798435396","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798435532","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579261,"feature_type":"variation","strand":1,"end":140579262,"alleles":["CC","C"]},{"seq_region_name":"7","id":"rs1798435649","clinical_significance":[],"strand":1,"feature_type":"variation","end":140579263,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579263,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579265,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140579265,"seq_region_name":"7","id":"rs1393197230","clinical_significance":[]},{"end":140579268,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140579268,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1324157138","clinical_significance":[]},{"alleles":["C","T"],"end":140579270,"feature_type":"variation","strand":1,"source":"dbSNP","start":140579270,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs920047550"},{"source":"dbSNP","start":140579271,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140579271,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1221647101"},{"seq_region_name":"7","id":"rs1798436206","clinical_significance":[],"start":140579275,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140579275,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579277,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140579277,"seq_region_name":"7","id":"rs1335323679","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579278,"source":"dbSNP","strand":1,"feature_type":"variation","end":140579278,"alleles":["C","A","T"],"seq_region_name":"7","id":"rs557410888","clinical_significance":[]},{"start":140579279,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140579279,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs575892407","clinical_significance":[]},{"seq_region_name":"7","id":"rs1384123783","clinical_significance":[],"end":140579283,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140579283,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1055453132","clinical_significance":[],"end":140579286,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140579286,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["AATAATAATAATAATAATAATAA","AATAATAATAATAATAA","AATAATAATAATAATAATAA","AATAATAATAATAATAATAATAATAA","AATAATAATAATAATAATAATAATAATAA"],"end":140579316,"strand":1,"feature_type":"variation","start":140579294,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs199505480","clinical_significance":[]},{"id":"rs1798437099","seq_region_name":"7","clinical_significance":[],"end":140579300,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140579300,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140579305,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579305,"source":"dbSNP","id":"rs1798437190","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798437295","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579308,"source":"dbSNP","strand":1,"feature_type":"variation","end":140579308,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1245023103","source":"dbSNP","start":140579311,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140579311,"alleles":["T","A"],"feature_type":"variation","strand":1},{"alleles":["T","-"],"end":140579311,"strand":1,"feature_type":"variation","start":140579311,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1356976656","clinical_significance":[]},{"end":140579313,"alleles":["AA","AAA"],"strand":1,"feature_type":"variation","start":140579312,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1798437612","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1251805020","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579313,"feature_type":"variation","strand":1,"alleles":["ATA","A"],"end":140579315},{"feature_type":"variation","strand":1,"end":140579314,"alleles":["T","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579314,"clinical_significance":[],"seq_region_name":"7","id":"rs553597"},{"strand":1,"feature_type":"variation","end":140579314,"alleles":["T","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579314,"source":"dbSNP","seq_region_name":"7","id":"rs941369151","clinical_significance":[]},{"seq_region_name":"7","id":"rs998257011","clinical_significance":[],"alleles":["A","G"],"end":140579315,"strand":1,"feature_type":"variation","start":140579315,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1554472711","clinical_significance":[],"start":140579315,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140579316,"alleles":["AA","AATAAAAA"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140579315,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140579319,"alleles":["AAAAA","AAAAAA","AAAAAAAA"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs897267437"},{"seq_region_name":"7","id":"rs1798438557","clinical_significance":[],"start":140579317,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140579317,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1029869161","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579320,"feature_type":"variation","strand":1,"end":140579320,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1244450402","feature_type":"variation","strand":1,"end":140579320,"alleles":["G","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579320},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798438904","source":"dbSNP","start":140579322,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140579322,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140579324,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140579324,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs912718908"},{"seq_region_name":"7","id":"rs1193502002","clinical_significance":[],"alleles":["A","G","T"],"end":140579330,"strand":1,"feature_type":"variation","start":140579330,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1251671157","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579333,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140579333},{"seq_region_name":"7","id":"rs555129832","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579335,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140579335},{"clinical_significance":[],"seq_region_name":"7","id":"rs1305966728","feature_type":"variation","strand":1,"end":140579341,"alleles":["T","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579341},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579343,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140579343,"seq_region_name":"7","id":"rs1039985424","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs921484553","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579344,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140579344},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579348,"feature_type":"variation","strand":1,"end":140579348,"alleles":["A","C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1798439748"},{"start":140579352,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140579352,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585678358","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140579359,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579359,"clinical_significance":[],"seq_region_name":"7","id":"rs1798440006"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798440105","source":"dbSNP","start":140579360,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140579360,"alleles":["C","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1033688871","source":"dbSNP","start":140579373,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140579373,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140579375,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579375,"source":"dbSNP","seq_region_name":"7","id":"rs1334859686","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs189908462","alleles":["C","T"],"end":140579377,"feature_type":"variation","strand":1,"source":"dbSNP","start":140579377,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1798440538","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140579380,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579380,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140579385,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579385,"clinical_significance":[],"id":"rs936338590","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1401712196","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579390,"source":"dbSNP","strand":1,"feature_type":"variation","end":140579390,"alleles":["A","T"]},{"source":"dbSNP","start":140579393,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140579393,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1011009856","seq_region_name":"7"},{"clinical_significance":[],"id":"rs375659092","seq_region_name":"7","alleles":["C","G","T"],"end":140579398,"feature_type":"variation","strand":1,"source":"dbSNP","start":140579398,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1585678457","clinical_significance":[],"start":140579399,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140579399,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs58295791","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["TTTTTTTTTTTT","TTTTTTTTT","TTTTTTTTTT","TTTTTTTTTTT","TTTTTTTTTTTTT","TTTTTTTTTTTTTT"],"end":140579410,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579399,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1443162187","clinical_significance":[],"strand":1,"feature_type":"variation","end":140579400,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579400,"source":"dbSNP"},{"start":140579402,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140579402,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798441658","clinical_significance":[]},{"start":140579410,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140579411,"alleles":["TG","-"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs200972682","clinical_significance":[]},{"seq_region_name":"7","id":"rs775087874","clinical_significance":[],"start":140579410,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140579412,"alleles":["TGA","-"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1183424307","source":"dbSNP","start":140579411,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140579411,"alleles":["G","C","T"],"feature_type":"variation","strand":1},{"end":140579411,"alleles":["G","-"],"strand":1,"feature_type":"variation","start":140579411,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1251223334","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579415,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140579415,"seq_region_name":"7","id":"rs1479495776","clinical_significance":[]},{"seq_region_name":"7","id":"rs1374076440","clinical_significance":[],"strand":1,"feature_type":"variation","end":140579416,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579416,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs182524577","alleles":["A","C","G"],"end":140579417,"feature_type":"variation","strand":1,"source":"dbSNP","start":140579417,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140579420,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TCTCTCTCT","TCTCT"],"end":140579428,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1463979391"},{"id":"rs892250886","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579426,"source":"dbSNP","strand":1,"feature_type":"variation","end":140579426,"alleles":["T","A","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs552844057","source":"dbSNP","start":140579429,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140579429,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140579431,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579431,"clinical_significance":[],"seq_region_name":"7","id":"rs1798442999"},{"seq_region_name":"7","id":"rs1336453496","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579432,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140579432},{"seq_region_name":"7","id":"rs1166187158","clinical_significance":[],"start":140579434,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140579434,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1309737339","clinical_significance":[],"alleles":["G","T"],"end":140579437,"strand":1,"feature_type":"variation","start":140579437,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140579442,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140579442,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585678600"},{"seq_region_name":"7","id":"rs1020561365","clinical_significance":[],"start":140579444,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140579444,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"alleles":["T","G"],"end":140579445,"feature_type":"variation","strand":1,"source":"dbSNP","start":140579445,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585678635"},{"id":"rs1798443749","seq_region_name":"7","clinical_significance":[],"start":140579449,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140579449,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579453,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","C","G"],"end":140579453,"id":"rs1585678653","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579455,"feature_type":"variation","strand":1,"end":140579455,"alleles":["G","C"],"clinical_significance":[],"id":"rs1396156436","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798444144","end":140579456,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140579456,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140579460,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579460,"clinical_significance":[],"seq_region_name":"7","id":"rs1798444251"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130627567","alleles":["A","G"],"end":140579462,"feature_type":"variation","strand":1,"source":"dbSNP","start":140579462,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798444363","feature_type":"variation","strand":1,"end":140579469,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579469},{"seq_region_name":"7","id":"rs1009729922","clinical_significance":[],"start":140579470,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140579470,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1294547378","alleles":["C","T"],"end":140579471,"feature_type":"variation","strand":1,"source":"dbSNP","start":140579471,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1798444697","clinical_significance":[],"start":140579473,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140579473,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140579474,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579474,"source":"dbSNP","id":"rs1046111139","seq_region_name":"7","clinical_significance":[]},{"end":140579475,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140579475,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs981820761","clinical_significance":[]},{"end":140579476,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140579476,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798445056","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs927677012","end":140579477,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140579477,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579478,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140579478,"clinical_significance":[],"seq_region_name":"7","id":"rs188272343"},{"end":140579479,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140579479,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1183825692"},{"strand":1,"feature_type":"variation","end":140579480,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579480,"source":"dbSNP","seq_region_name":"7","id":"rs1798445412","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579481,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140579481,"clinical_significance":[],"id":"rs1417303067","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1798445623","clinical_significance":[],"alleles":["C","G"],"end":140579483,"strand":1,"feature_type":"variation","start":140579483,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798445735","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579490,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140579490},{"strand":1,"feature_type":"variation","end":140579496,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579496,"source":"dbSNP","seq_region_name":"7","id":"rs1249548959","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs532804186","feature_type":"variation","strand":1,"end":140579497,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579497},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579503,"source":"dbSNP","strand":1,"feature_type":"variation","end":140579503,"alleles":["C","T"],"seq_region_name":"7","id":"rs1222999236","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798446195","feature_type":"variation","strand":1,"end":140579504,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579504},{"start":140579509,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140579509,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs868728660","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579512,"feature_type":"variation","strand":1,"end":140579512,"alleles":["C","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1033575142"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1289802939","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140579515,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579515},{"clinical_significance":[],"id":"rs1798446631","seq_region_name":"7","end":140579517,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140579517,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140579518,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579518,"clinical_significance":[],"seq_region_name":"7","id":"rs1798446748"},{"strand":1,"feature_type":"variation","end":140579519,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579519,"source":"dbSNP","id":"rs1222066064","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579520,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140579520,"id":"rs544983645","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140579524,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579524,"clinical_significance":[],"seq_region_name":"7","id":"rs1798447083"},{"end":140579528,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140579528,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130627757","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798447201","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140579530,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579530,"source":"dbSNP"},{"alleles":["T","C"],"end":140579531,"feature_type":"variation","strand":1,"source":"dbSNP","start":140579531,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130627770"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579532,"source":"dbSNP","strand":1,"feature_type":"variation","end":140579532,"alleles":["A","G"],"id":"rs1798447345","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","T"],"end":140579533,"feature_type":"variation","strand":1,"source":"dbSNP","start":140579533,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs563462028"},{"clinical_significance":[],"id":"rs1351409430","seq_region_name":"7","source":"dbSNP","start":140579534,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140579534,"feature_type":"variation","strand":1},{"start":140579536,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140579536,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs1798447887","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs77780088","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579537,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140579537},{"strand":1,"feature_type":"variation","end":140579538,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579538,"source":"dbSNP","seq_region_name":"7","id":"rs1027392346","clinical_significance":[]},{"seq_region_name":"7","id":"rs941269649","clinical_significance":[],"end":140579540,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140579540,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579543,"feature_type":"variation","strand":1,"end":140579543,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1798448754"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579544,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140579544,"id":"rs1335758440","seq_region_name":"7","clinical_significance":[]},{"start":140579545,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140579545,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798449046","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798449150","end":140579550,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140579550,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1037063529","seq_region_name":"7","source":"dbSNP","start":140579553,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140579553,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs191570562","clinical_significance":[],"alleles":["G","A"],"end":140579554,"strand":1,"feature_type":"variation","start":140579554,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579555,"feature_type":"variation","strand":1,"end":140579555,"alleles":["G","C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs183825767"},{"clinical_significance":[],"seq_region_name":"7","id":"rs983273674","alleles":["C","G"],"end":140579556,"feature_type":"variation","strand":1,"source":"dbSNP","start":140579556,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1300822070","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579560,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140579560},{"strand":1,"feature_type":"variation","end":140579564,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579564,"source":"dbSNP","id":"rs1225183738","seq_region_name":"7","clinical_significance":[]},{"id":"rs1385030608","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140579565,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579565,"source":"dbSNP"},{"id":"rs140782849","seq_region_name":"7","clinical_significance":[],"start":140579573,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140579573,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579576,"feature_type":"variation","strand":1,"alleles":["AGAGA","AGA"],"end":140579580,"clinical_significance":[],"seq_region_name":"7","id":"rs1451499192"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579576,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AGAGA","-"],"end":140579580,"id":"rs1798450225","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1051184349","end":140579578,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140579578,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579579,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140579579,"id":"rs889843745","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1007483860","clinical_significance":[],"strand":1,"feature_type":"variation","end":140579580,"alleles":["A","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579580,"source":"dbSNP"},{"source":"dbSNP","start":140579581,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140579581,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs547078887"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579581,"source":"dbSNP","strand":1,"feature_type":"variation","end":140579581,"alleles":["C","CTCC"],"seq_region_name":"7","id":"rs1798450793","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs150138608","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579582,"feature_type":"variation","strand":1,"end":140579582,"alleles":["G","A"]},{"end":140579584,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140579584,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798451001","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585679034","clinical_significance":[],"start":140579586,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140579586,"strand":1,"feature_type":"variation"},{"end":140579594,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140579594,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1260848209","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798451336","feature_type":"variation","strand":1,"end":140579597,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579597},{"seq_region_name":"7","id":"rs1263942473","clinical_significance":[],"end":140579608,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140579608,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs765846794","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579610,"feature_type":"variation","strand":1,"alleles":["T","A","G"],"end":140579610},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579612,"source":"dbSNP","strand":1,"feature_type":"variation","end":140579612,"alleles":["C","T"],"id":"rs975553894","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","G"],"end":140579613,"strand":1,"feature_type":"variation","start":140579613,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1203514808","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798451886","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140579615,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579615,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2536956","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579616,"feature_type":"variation","strand":1,"end":140579616,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1798452153","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579618,"source":"dbSNP","strand":1,"feature_type":"variation","end":140579618,"alleles":["C","T"]},{"id":"rs1798452255","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579619,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140579619},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798452357","feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140579623,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579623},{"clinical_significance":[],"seq_region_name":"7","id":"rs1200165885","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579624,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140579624},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579627,"feature_type":"variation","strand":1,"end":140579627,"alleles":["A","C"],"clinical_significance":[],"id":"rs1262899995","seq_region_name":"7"},{"alleles":["G","C"],"end":140579628,"strand":1,"feature_type":"variation","start":140579628,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1020613608","clinical_significance":[]},{"end":140579629,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140579629,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798452782"},{"seq_region_name":"7","id":"rs1321774850","clinical_significance":[],"end":140579631,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140579631,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140579635,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579635,"source":"dbSNP","id":"rs1283104834","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140579636,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140579636,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs114978814"},{"feature_type":"variation","strand":1,"end":140579640,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579640,"clinical_significance":[],"seq_region_name":"7","id":"rs1798453284"},{"feature_type":"variation","strand":1,"end":140579641,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579641,"clinical_significance":[],"seq_region_name":"7","id":"rs1798453384"},{"clinical_significance":[],"seq_region_name":"7","id":"rs138877548","feature_type":"variation","strand":1,"end":140579644,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579644},{"clinical_significance":[],"seq_region_name":"7","id":"rs1034742789","alleles":["G","A"],"end":140579645,"feature_type":"variation","strand":1,"source":"dbSNP","start":140579645,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs913563341","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579647,"feature_type":"variation","strand":1,"end":140579647,"alleles":["C","A","T"]},{"alleles":["C","T"],"end":140579660,"strand":1,"feature_type":"variation","start":140579660,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1176987676","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1470924137","source":"dbSNP","start":140579661,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140579663,"alleles":["AAA","AA"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140579670,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140579670,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs945029672","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1672211403","feature_type":"variation","strand":1,"end":140579676,"alleles":["AAAAAAA","AAAAAA","AAAAAAAA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579670},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798454224","feature_type":"variation","strand":1,"end":140579677,"alleles":["T","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579677},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140579678,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579678,"source":"dbSNP","seq_region_name":"7","id":"rs1426927693","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140579681,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579681,"source":"dbSNP","seq_region_name":"7","id":"rs188713967","clinical_significance":[]},{"seq_region_name":"7","id":"rs1046584574","clinical_significance":[],"start":140579682,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140579682,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1175526787","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579683,"feature_type":"variation","strand":1,"end":140579683,"alleles":["C","G"]},{"seq_region_name":"7","id":"rs1335830149","clinical_significance":[],"alleles":["C","A","T"],"end":140579687,"strand":1,"feature_type":"variation","start":140579687,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140579688,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579688,"clinical_significance":[],"seq_region_name":"7","id":"rs991083302"},{"seq_region_name":"7","id":"rs2130628291","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579688,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AT","-"],"end":140579689},{"seq_region_name":"7","id":"rs1191337164","clinical_significance":[],"start":140579689,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140579689,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1585679257","clinical_significance":[],"strand":1,"feature_type":"variation","end":140579692,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579692,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140579700,"alleles":["AACA","AACAACA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579697,"source":"dbSNP","seq_region_name":"7","id":"rs1798455210","clinical_significance":[]},{"end":140579705,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140579705,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798455318","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579707,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140579707,"id":"rs758987565","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs192621004","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140579708,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579708},{"end":140579709,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140579709,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1206105135"},{"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140579718,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579718,"clinical_significance":[],"seq_region_name":"7","id":"rs567079525"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579719,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140579719,"id":"rs972641998","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130628373","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579720,"source":"dbSNP","strand":1,"feature_type":"variation","end":140579720,"alleles":["A","C"]},{"source":"dbSNP","start":140579726,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140579726,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs747449771"},{"end":140579728,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140579728,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1404098855"},{"clinical_significance":[],"seq_region_name":"7","id":"rs994709060","source":"dbSNP","start":140579730,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140579730,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1798456802","clinical_significance":[],"alleles":["G","T"],"end":140579732,"strand":1,"feature_type":"variation","start":140579732,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1363754088","feature_type":"variation","strand":1,"end":140579739,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579739},{"start":140579740,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140579740,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs768914297","clinical_significance":[]},{"seq_region_name":"7","id":"rs1026191645","clinical_significance":[],"alleles":["A","G"],"end":140579746,"strand":1,"feature_type":"variation","start":140579746,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579748,"source":"dbSNP","strand":1,"feature_type":"variation","end":140579748,"alleles":["A","C"],"id":"rs1403870845","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140579749,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140579749,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130628448"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140579752,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579752,"source":"dbSNP","seq_region_name":"7","id":"rs370104601","clinical_significance":[]},{"seq_region_name":"7","id":"rs1051065121","clinical_significance":[],"start":140579755,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AAA","A"],"end":140579757,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1421433611","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579757,"feature_type":"variation","strand":1,"end":140579757,"alleles":["A","G"]},{"clinical_significance":[],"id":"rs911314296","seq_region_name":"7","alleles":["T","C"],"end":140579759,"feature_type":"variation","strand":1,"source":"dbSNP","start":140579759,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140579760,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140579760,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs942783923","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1385934034","feature_type":"variation","strand":1,"end":140579763,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579763},{"clinical_significance":[],"id":"rs184787093","seq_region_name":"7","alleles":["G","T"],"end":140579764,"feature_type":"variation","strand":1,"source":"dbSNP","start":140579764,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1443298820","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579767,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140579767},{"strand":1,"feature_type":"variation","end":140579770,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579770,"source":"dbSNP","seq_region_name":"7","id":"rs2130628532","clinical_significance":[]},{"end":140579771,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140579771,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798458162"},{"clinical_significance":[],"seq_region_name":"7","id":"rs552696117","alleles":["T","C"],"end":140579772,"feature_type":"variation","strand":1,"source":"dbSNP","start":140579772,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579773,"source":"dbSNP","strand":1,"feature_type":"variation","end":140579773,"alleles":["G","A","T"],"seq_region_name":"7","id":"rs1004185582","clinical_significance":[]},{"seq_region_name":"7","id":"rs1205841857","clinical_significance":[],"end":140579779,"alleles":["GGGG","GGGGG"],"strand":1,"feature_type":"variation","start":140579776,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579778,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140579778,"seq_region_name":"7","id":"rs1798458634","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579779,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140579779,"id":"rs2130628575","seq_region_name":"7","clinical_significance":[]},{"id":"rs1439880596","seq_region_name":"7","clinical_significance":[],"end":140579784,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140579784,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140579785,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579785,"source":"dbSNP","seq_region_name":"7","id":"rs1020133121","clinical_significance":[]},{"source":"dbSNP","start":140579788,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140579788,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1798458984","seq_region_name":"7"},{"clinical_significance":[],"id":"rs116829353","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579789,"feature_type":"variation","strand":1,"end":140579789,"alleles":["C","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579790,"feature_type":"variation","strand":1,"end":140579790,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1341068862"},{"start":140579795,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AAGAAGA","AAGA"],"end":140579801,"strand":1,"feature_type":"variation","id":"rs1798459263","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140579799,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579799,"source":"dbSNP","seq_region_name":"7","id":"rs2130628640","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798459394","end":140579801,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140579801,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs544709332","clinical_significance":[],"end":140579803,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140579803,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798459627","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579805,"feature_type":"variation","strand":1,"end":140579805,"alleles":["T","G"]},{"seq_region_name":"7","id":"rs1028494827","clinical_significance":[],"strand":1,"feature_type":"variation","end":140579811,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579811,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1798459856","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579812,"feature_type":"variation","strand":1,"end":140579820,"alleles":["ACACACACA","ACACACACACA"]},{"end":140579813,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140579813,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798460056"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1379956350","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579814,"feature_type":"variation","strand":1,"end":140579814,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798460441","feature_type":"variation","strand":1,"end":140579819,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579819},{"clinical_significance":[],"id":"rs907435102","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140579820,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579820},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140579821,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579821,"clinical_significance":[],"id":"rs1798460751","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140579826,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579826,"clinical_significance":[],"seq_region_name":"7","id":"rs1798460855"},{"alleles":["C","T"],"end":140579827,"feature_type":"variation","strand":1,"source":"dbSNP","start":140579827,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs114550789"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1356044391","feature_type":"variation","strand":1,"end":140579829,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579829},{"end":140579831,"alleles":["T","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140579831,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1326656815"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1429347180","feature_type":"variation","strand":1,"end":140579833,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579833},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798461442","alleles":["A","C"],"end":140579834,"feature_type":"variation","strand":1,"source":"dbSNP","start":140579834,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140579836,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579836,"source":"dbSNP","seq_region_name":"7","id":"rs575468750","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs748231170","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579838,"feature_type":"variation","strand":1,"end":140579838,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1034671083","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140579840,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579840,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798461947","source":"dbSNP","start":140579842,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140579842,"alleles":["T","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585679570","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140579846,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579846},{"clinical_significance":[],"seq_region_name":"7","id":"rs1422752071","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579849,"feature_type":"variation","strand":1,"end":140579849,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs769710892","source":"dbSNP","start":140579850,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140579850,"alleles":["G","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs894916941","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579852,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140579852},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563155445","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579853,"feature_type":"variation","strand":1,"end":140579853,"alleles":["C","A","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579857,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140579857,"clinical_significance":[],"seq_region_name":"7","id":"rs773290638"},{"alleles":["G","A","T"],"end":140579858,"feature_type":"variation","strand":1,"source":"dbSNP","start":140579858,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs759398620","seq_region_name":"7"},{"id":"rs1798462940","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140579862,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579862,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["C","A","G"],"end":140579867,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579867,"source":"dbSNP","seq_region_name":"7","id":"rs534369929","clinical_significance":[]},{"end":140579869,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140579869,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1482515547"},{"seq_region_name":"7","id":"rs772060177","clinical_significance":[],"end":140579870,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140579870,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140579871,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140579871,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130628891"},{"source":"dbSNP","start":140579873,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140579875,"alleles":["TGT","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1798463484","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798463596","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579874,"feature_type":"variation","strand":1,"end":140579873,"alleles":["-","C"]},{"alleles":["G","A"],"end":140579874,"feature_type":"variation","strand":1,"source":"dbSNP","start":140579874,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798463718"},{"strand":1,"feature_type":"variation","alleles":["TAATCCAA","-"],"end":140579882,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579875,"source":"dbSNP","id":"rs1798463833","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs962540213","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579876,"feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140579876},{"id":"rs972528144","seq_region_name":"7","clinical_significance":[],"end":140579879,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140579879,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["A","G"],"end":140579881,"feature_type":"variation","strand":1,"source":"dbSNP","start":140579881,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798464217"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579882,"source":"dbSNP","strand":1,"feature_type":"variation","end":140579882,"alleles":["A","G"],"seq_region_name":"7","id":"rs1025580902","clinical_significance":[]},{"clinical_significance":[],"id":"rs1798464473","seq_region_name":"7","feature_type":"variation","strand":1,"end":140579883,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579883},{"start":140579887,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140579887,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798464585","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140579888,"alleles":["-","CG"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579889,"clinical_significance":[],"seq_region_name":"7","id":"rs1798464693"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140579891,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579891,"source":"dbSNP","id":"rs1798464813","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140579893,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140579893,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798464938"},{"end":140579895,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140579895,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1224246480"},{"seq_region_name":"7","id":"rs1798465218","clinical_significance":[],"start":140579897,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140579897,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579897,"feature_type":"variation","strand":1,"alleles":["AAA","AA"],"end":140579899,"clinical_significance":[],"seq_region_name":"7","id":"rs1798465398"},{"source":"dbSNP","start":140579898,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140579898,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798465595"},{"id":"rs955252488","seq_region_name":"7","clinical_significance":[],"end":140579900,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140579900,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1277545718","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579903,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140579903},{"source":"dbSNP","start":140579904,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140579904,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798465977"},{"source":"dbSNP","start":140579906,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140579906,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs927747554","seq_region_name":"7"},{"start":140579907,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140579907,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798466357","clinical_significance":[]},{"end":140579910,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140579910,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1345920563"},{"seq_region_name":"7","id":"rs1585679709","clinical_significance":[],"alleles":["A","C"],"end":140579912,"strand":1,"feature_type":"variation","start":140579912,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579913,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140579913,"seq_region_name":"7","id":"rs1798466908","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798467111","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579914,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140579914},{"clinical_significance":[],"seq_region_name":"7","id":"rs937755604","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579915,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140579915},{"clinical_significance":[],"id":"rs1798467466","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140579916,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579916},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130629112","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579920,"feature_type":"variation","strand":1,"end":140579920,"alleles":["T","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1263084326","alleles":["A","G"],"end":140579922,"feature_type":"variation","strand":1,"source":"dbSNP","start":140579922,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798467854","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579930,"feature_type":"variation","strand":1,"end":140579930,"alleles":["A","C","G"]},{"alleles":["A","G"],"end":140579931,"feature_type":"variation","strand":1,"source":"dbSNP","start":140579931,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1798468050","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579933,"feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140579933,"clinical_significance":[],"id":"rs911215117","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1054922311","source":"dbSNP","start":140579934,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140579934,"alleles":["C","A"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140579935,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579935,"clinical_significance":[],"id":"rs942815652","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1798468665","clinical_significance":[],"end":140579937,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140579937,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs899005107","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140579939,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579939},{"alleles":["G","A"],"end":140579942,"strand":1,"feature_type":"variation","start":140579942,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1798468887","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140579949,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140579949,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798468987"},{"feature_type":"variation","strand":1,"end":140579985,"alleles":["ATGAAACCCCGTCTCTACTAAAAATACAAAAAAAT","AT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579951,"clinical_significance":[],"seq_region_name":"7","id":"rs1798469096"},{"start":140579952,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140579952,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585679783","clinical_significance":[]},{"end":140579956,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140579956,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585679788"},{"seq_region_name":"7","id":"rs1798469442","clinical_significance":[],"alleles":["C","A"],"end":140579958,"strand":1,"feature_type":"variation","start":140579958,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1798469551","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579959,"source":"dbSNP","strand":1,"feature_type":"variation","end":140579959,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1402946495","feature_type":"variation","strand":1,"end":140579960,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579960},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579961,"feature_type":"variation","strand":1,"end":140579961,"alleles":["G","A","T"],"clinical_significance":[],"id":"rs145732034","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs775252322","source":"dbSNP","start":140579963,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140579963,"alleles":["C","A"],"feature_type":"variation","strand":1},{"id":"rs1798470038","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140579968,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579968,"source":"dbSNP"},{"start":140579969,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140579969,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798470164","clinical_significance":[]},{"seq_region_name":"7","id":"rs367728910","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579973,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140579973},{"clinical_significance":[],"seq_region_name":"7","id":"rs1432724612","alleles":["T","C"],"end":140579975,"feature_type":"variation","strand":1,"source":"dbSNP","start":140579975,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1798470506","clinical_significance":[],"strand":1,"feature_type":"variation","end":140579976,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579976,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140579977,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140579977,"source":"dbSNP","id":"rs535335883","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579978,"feature_type":"variation","strand":1,"alleles":["AAAAAAA","AAAAAAAA"],"end":140579984,"clinical_significance":[],"seq_region_name":"7","id":"rs1798470859"},{"seq_region_name":"7","id":"rs1271531144","clinical_significance":[],"start":140579982,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140579982,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs201739071","source":"dbSNP","start":140579983,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140579983,"feature_type":"variation","strand":1},{"start":140579985,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140579985,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798471368","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798471598","clinical_significance":[],"start":140579988,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140579988,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"end":140579990,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140579990,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs142871828","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1041842552","end":140579991,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140579991,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1245624557","seq_region_name":"7","feature_type":"variation","strand":1,"end":140579992,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140579992},{"id":"rs1004643902","seq_region_name":"7","clinical_significance":[],"end":140579993,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140579993,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140579995,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140579995,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs528337766","seq_region_name":"7"},{"start":140579999,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140579999,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798472707","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140580001,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580001,"source":"dbSNP","seq_region_name":"7","id":"rs760434703","clinical_significance":[]},{"id":"rs546815264","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580004,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140580004},{"seq_region_name":"7","id":"rs1227742724","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580006,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140580006},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580007,"source":"dbSNP","strand":1,"feature_type":"variation","end":140580007,"alleles":["G","A"],"seq_region_name":"7","id":"rs1798473268","clinical_significance":[]},{"id":"rs1798473455","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140580008,"strand":1,"feature_type":"variation","start":140580008,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs996938978","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140580010,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580010,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798473672","feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140580011,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580011},{"clinical_significance":[],"seq_region_name":"7","id":"rs1028380180","source":"dbSNP","start":140580012,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140580012,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs12334204","seq_region_name":"7","end":140580013,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140580013,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1585679948","seq_region_name":"7","clinical_significance":[],"alleles":["G","C"],"end":140580014,"strand":1,"feature_type":"variation","start":140580014,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1011051077","clinical_significance":[],"start":140580015,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140580015,"alleles":["T","G"],"strand":1,"feature_type":"variation"},{"alleles":["A","G"],"end":140580019,"strand":1,"feature_type":"variation","start":140580019,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798474283","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798474391","alleles":["C","A"],"end":140580021,"feature_type":"variation","strand":1,"source":"dbSNP","start":140580021,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1406728238","clinical_significance":[],"end":140580025,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140580025,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["G","A"],"end":140580029,"feature_type":"variation","strand":1,"source":"dbSNP","start":140580029,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798474632"},{"alleles":["A","G"],"end":140580030,"strand":1,"feature_type":"variation","start":140580030,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1012286337","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs532625734","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580033,"source":"dbSNP","strand":1,"feature_type":"variation","end":140580033,"alleles":["C","T"]},{"alleles":["T","C"],"end":140580034,"strand":1,"feature_type":"variation","start":140580034,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798475015","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580038,"source":"dbSNP","strand":1,"feature_type":"variation","end":140580038,"alleles":["A","G"],"id":"rs1798475188","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140580044,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140580044,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798475366"},{"clinical_significance":[],"id":"rs1367249636","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580047,"feature_type":"variation","strand":1,"end":140580047,"alleles":["G","C"]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140580051,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580051,"source":"dbSNP","seq_region_name":"7","id":"rs1300687735","clinical_significance":[]},{"seq_region_name":"7","id":"rs550715799","clinical_significance":[],"start":140580052,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140580052,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs2130629547","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580054,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140580054},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798475894","end":140580055,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140580055,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140580056,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140580056,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1016692567"},{"clinical_significance":[],"seq_region_name":"7","id":"rs758916918","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580059,"feature_type":"variation","strand":1,"end":140580059,"alleles":["G","A"]},{"source":"dbSNP","start":140580064,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140580064,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1021649376","seq_region_name":"7"},{"alleles":["C","A","T"],"end":140580066,"feature_type":"variation","strand":1,"source":"dbSNP","start":140580066,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs569184590"},{"clinical_significance":[],"id":"rs1308691379","seq_region_name":"7","source":"dbSNP","start":140580073,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140580073,"feature_type":"variation","strand":1},{"alleles":["G","C","T"],"end":140580079,"feature_type":"variation","strand":1,"source":"dbSNP","start":140580079,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585680055"},{"seq_region_name":"7","id":"rs966975397","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580086,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140580086},{"id":"rs1314823473","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580088,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140580088},{"seq_region_name":"7","id":"rs1798476966","clinical_significance":[],"strand":1,"feature_type":"variation","end":140580092,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580092,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1470599746","source":"dbSNP","start":140580097,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140580097,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs994020468","source":"dbSNP","start":140580100,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140580100,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1798477177","seq_region_name":"7","alleles":["C","A"],"end":140580102,"feature_type":"variation","strand":1,"source":"dbSNP","start":140580102,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140580104,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140580104,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1174815199","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140580108,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580108,"source":"dbSNP","seq_region_name":"7","id":"rs1798477401","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1186749424","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140580109,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580109},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580109,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AAAAAAAAA","AAAAAAAA","AAAAAAAAAA"],"end":140580117,"seq_region_name":"7","id":"rs556294250","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798477771","clinical_significance":[],"alleles":["A","C"],"end":140580112,"strand":1,"feature_type":"variation","start":140580112,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1486539664","clinical_significance":[],"alleles":["A","T"],"end":140580115,"strand":1,"feature_type":"variation","start":140580115,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798478034","source":"dbSNP","start":140580117,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140580117,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580117,"feature_type":"variation","strand":1,"alleles":["ATG","TT"],"end":140580119,"clinical_significance":[],"seq_region_name":"7","id":"rs386718482"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580118,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140580118,"seq_region_name":"7","id":"rs1798478263","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs536552545","feature_type":"variation","strand":1,"end":140580119,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580119},{"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140580120,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580120,"source":"dbSNP","id":"rs1208008031","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798478629","source":"dbSNP","start":140580122,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140580122,"alleles":["A","T"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140580125,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580125,"source":"dbSNP","seq_region_name":"7","id":"rs75009028","clinical_significance":[]},{"seq_region_name":"7","id":"rs1264765870","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580126,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140580126},{"id":"rs1230867360","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140580129,"strand":1,"feature_type":"variation","start":140580129,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140580138,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140580138,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1267432937","clinical_significance":[]},{"alleles":["G","A"],"end":140580151,"strand":1,"feature_type":"variation","start":140580151,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798479222","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140580152,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580152,"clinical_significance":[],"seq_region_name":"7","id":"rs1311401984"},{"seq_region_name":"7","id":"rs1798479474","clinical_significance":[],"start":140580156,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AAA","AAAAA"],"end":140580158,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1798479600","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580160,"feature_type":"variation","strand":1,"end":140580160,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs1296477851","clinical_significance":[],"strand":1,"feature_type":"variation","end":140580162,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580162,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1488197015","end":140580164,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140580164,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140580165,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140580165,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1216577850","clinical_significance":[]},{"alleles":["A","G"],"end":140580166,"strand":1,"feature_type":"variation","start":140580166,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1798480086","seq_region_name":"7","clinical_significance":[]},{"end":140580170,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140580170,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs958990645","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580171,"source":"dbSNP","strand":1,"feature_type":"variation","end":140580171,"alleles":["T","C"],"seq_region_name":"7","id":"rs1798480327","clinical_significance":[]},{"id":"rs753390755","seq_region_name":"7","clinical_significance":[],"end":140580174,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140580174,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140580177,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580177,"clinical_significance":[],"id":"rs1798480574","seq_region_name":"7"},{"clinical_significance":[],"id":"rs990537411","seq_region_name":"7","source":"dbSNP","start":140580178,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140580178,"alleles":["T","C"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580181,"source":"dbSNP","strand":1,"feature_type":"variation","end":140580181,"alleles":["T","C"],"seq_region_name":"7","id":"rs920315625","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs761551470","source":"dbSNP","start":140580184,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140580184,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs571960937","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140580185,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580185},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580186,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140580186,"clinical_significance":[],"seq_region_name":"7","id":"rs566819782"},{"start":140580189,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TTTTTTT","TTTTTT"],"end":140580195,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1335336729","clinical_significance":[]},{"seq_region_name":"7","id":"rs1465799292","clinical_significance":[],"strand":1,"feature_type":"variation","end":140580191,"alleles":["T","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580191,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580194,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140580194,"clinical_significance":[],"seq_region_name":"7","id":"rs1170650452"},{"feature_type":"variation","strand":1,"end":140580198,"alleles":["TT","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580197,"clinical_significance":[],"id":"rs1798481682","seq_region_name":"7"},{"start":140580206,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140580206,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs1798481809","seq_region_name":"7","clinical_significance":[]},{"id":"rs2130629909","seq_region_name":"7","clinical_significance":[],"start":140580210,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140580210,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs534149335","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580212,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140580212},{"clinical_significance":[],"seq_region_name":"7","id":"rs1385655582","feature_type":"variation","strand":1,"end":140580214,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580214},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798482150","source":"dbSNP","start":140580216,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140580216,"alleles":["A","C"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140580219,"alleles":["G","C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580219,"source":"dbSNP","seq_region_name":"7","id":"rs907810287","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs914679384","alleles":["C","G","T"],"end":140580225,"feature_type":"variation","strand":1,"source":"dbSNP","start":140580225,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["T","C"],"end":140580229,"strand":1,"feature_type":"variation","start":140580229,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130629956","clinical_significance":[]},{"alleles":["T","G"],"end":140580233,"strand":1,"feature_type":"variation","start":140580233,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130629963","clinical_significance":[]},{"clinical_significance":[],"id":"rs2130629971","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140580234,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580234},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580235,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140580235,"clinical_significance":[],"seq_region_name":"7","id":"rs1798482543"},{"strand":1,"feature_type":"variation","alleles":["T","A","G"],"end":140580239,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580239,"source":"dbSNP","seq_region_name":"7","id":"rs1798482661","clinical_significance":[]},{"id":"rs2130630004","seq_region_name":"7","clinical_significance":[],"start":140580242,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140580242,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs764783687","seq_region_name":"7","alleles":["A","G"],"end":140580243,"feature_type":"variation","strand":1,"source":"dbSNP","start":140580243,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798482909","alleles":["ACCAGAAAAACTTTAC","AC"],"end":140580258,"feature_type":"variation","strand":1,"source":"dbSNP","start":140580243,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1798483023","seq_region_name":"7","source":"dbSNP","start":140580244,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140580245,"alleles":["CC","C"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140580246,"alleles":["A","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580246,"source":"dbSNP","seq_region_name":"7","id":"rs1198665419","clinical_significance":[]},{"seq_region_name":"7","id":"rs1482781635","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580248,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140580248},{"clinical_significance":[],"seq_region_name":"7","id":"rs1040277315","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580251,"feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140580251},{"start":140580254,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140580254,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798483497","clinical_significance":[]},{"start":140580255,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140580267,"alleles":["TTACAATTACAAT","TTACAAT"],"strand":1,"feature_type":"variation","id":"rs1798483611","seq_region_name":"7","clinical_significance":[]},{"id":"rs1798483727","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140580256,"strand":1,"feature_type":"variation","start":140580256,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130630080","source":"dbSNP","start":140580258,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140580258,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580264,"feature_type":"variation","strand":1,"end":140580264,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1798483833"},{"end":140580267,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140580267,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs768092891","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1349293312","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140580269,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580269},{"feature_type":"variation","strand":1,"end":140580272,"alleles":["TTTT","TTTTT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580269,"clinical_significance":[],"id":"rs149988842","seq_region_name":"7"},{"start":140580276,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AAAAAAAA","AAAAAAA","AAAAAAAAA"],"end":140580283,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs572518794","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs535262441","source":"dbSNP","start":140580280,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140580280,"alleles":["A","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs996823459","seq_region_name":"7","feature_type":"variation","strand":1,"end":140580281,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580281},{"clinical_significance":[],"seq_region_name":"7","id":"rs1246734648","source":"dbSNP","start":140580281,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140580288,"alleles":["AAAGAAAG","AAAG"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140580288,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580288,"clinical_significance":[],"seq_region_name":"7","id":"rs1563155664"},{"clinical_significance":[],"seq_region_name":"7","id":"rs774040056","alleles":["GCATGTATGTATGCATGTATGTATGCATGTATG","GCATGTATGTATGCATGTATG","GCATGTATGTATGCATGTATGTATGCATGTATGTATGCATGTATG"],"end":140580321,"feature_type":"variation","strand":1,"source":"dbSNP","start":140580289,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140580290,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580290,"source":"dbSNP","seq_region_name":"7","id":"rs1563155675","clinical_significance":[]},{"start":140580290,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["CATGTATGTAT","CATGTATGTATACATGTATGTAT"],"end":140580300,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798485200","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585680492","clinical_significance":[],"start":140580293,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140580293,"strand":1,"feature_type":"variation"},{"alleles":["T","C"],"end":140580294,"feature_type":"variation","strand":1,"source":"dbSNP","start":140580294,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs749958183"},{"end":140580333,"alleles":["ATGTATGCATGTATGTATGCATGTATGCATGTATGTATG","ATGTATGCATGTATGTATG","ATGTATGCATGTATGTATGCATGTATGCATGTATGTATGCATGTATGCATGTATGTATG"],"strand":1,"feature_type":"variation","start":140580295,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1395983413","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140580298,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580298,"clinical_significance":[],"seq_region_name":"7","id":"rs62485835"},{"id":"rs1300310354","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140580301,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580301,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580302,"source":"dbSNP","strand":1,"feature_type":"variation","end":140580302,"alleles":["C","T"],"id":"rs62485836","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140580303,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140580313,"alleles":["ATGTATGTATG","ATGTATG","ATGTATGTATGTATG"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1167587498"},{"seq_region_name":"7","id":"rs186550575","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140580304,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580304,"source":"dbSNP"},{"end":140580306,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140580306,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs62485837"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1554472936","source":"dbSNP","start":140580307,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["ATG","ATGCATG","ATGCATGTATGTATGCATG"],"end":140580309,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798486596","end":140580311,"alleles":["ATGTA","ATGTAGGCATGTATGCATGTA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140580307,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140580329,"alleles":["ATGTATGCATGTATGCATGTATG","ATGTATGCATGTATG","ATGTATGCATGTATGCATGTATGCATGTATG","ATGTATGCATGTATGCATGTATGCATGTATGCATGTATG","ATGTATGCATGTATGCATGTATGCATGTATGCATGTATGCATGTATG","ATGTATGCATGTATGCATGTATGCATGTATGCATGTATGCATGTATGCATGTATG","ATGTATGCATGTATGCATGTATGCATGTATGCATGTATGCATGTATGCATGTATGCATGTATGCATGTATG","ATGTATGCATGTATGCATGTATGCATGTATGTATGCATGTATGCATGTATGCATGTATGCATGTATG"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580307,"clinical_significance":[],"seq_region_name":"7","id":"rs113910778"},{"seq_region_name":"7","id":"rs1798487088","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580307,"source":"dbSNP","strand":1,"feature_type":"variation","end":140580333,"alleles":["ATGTATGCATGTATGCATGTATGTATG","ATGTATGCATGTATGCATGTATGTATGCATGTATGCATGTATGCATGTATGCATGTATGTATG"]},{"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140580308,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580308,"source":"dbSNP","seq_region_name":"7","id":"rs893872136","clinical_significance":[]},{"seq_region_name":"7","id":"rs1223546530","clinical_significance":[],"start":140580310,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140580310,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140580311,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580311,"source":"dbSNP","id":"rs1798487428","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["ATGCATGTATGCATG","ATG"],"end":140580325,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580311,"clinical_significance":[],"id":"rs1798487536","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs947760325","feature_type":"variation","strand":1,"end":140580312,"alleles":["T","A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580312},{"strand":1,"feature_type":"variation","alleles":["TGCATGTATGCATGT","TGCATGTATGCATGTGTGCATGTATGCATGT"],"end":140580326,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580312,"source":"dbSNP","seq_region_name":"7","id":"rs1798487781","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140580314,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580314,"clinical_significance":[],"seq_region_name":"7","id":"rs1361620130"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580317,"source":"dbSNP","strand":1,"feature_type":"variation","end":140580329,"alleles":["GTATGCATGTATG","GTATGCATGTATGCACGTATGCATGTATG"],"id":"rs1263811113","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798488095","clinical_significance":[],"start":140580320,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140580320,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580322,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140580322,"seq_region_name":"7","id":"rs1336940840","clinical_significance":[]},{"start":140580323,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["ATGTATG","ATGTATGCATGTATGTATGTATG"],"end":140580329,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798488308","clinical_significance":[]},{"end":140580336,"alleles":["ATGTATGTATGTAT","ATGTATGTAT","ATGTATGTATGTATGTAT"],"strand":1,"feature_type":"variation","start":140580323,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1244660190","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580324,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140580324,"clinical_significance":[],"id":"rs1038420839","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140580326,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580326,"clinical_significance":[],"seq_region_name":"7","id":"rs1350257619"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1405199988","feature_type":"variation","strand":1,"end":140580327,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580327},{"start":140580327,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140580329,"alleles":["ATG","ATGCATG","ATGCATGTATGCATG","ATGCATGTATGCATGCATG"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1306980024","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563155721","feature_type":"variation","strand":1,"alleles":["TG","TGCATGTATTG"],"end":140580329,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580328},{"start":140580330,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140580329,"alleles":["-","CA"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1315369229","clinical_significance":[]},{"seq_region_name":"7","id":"rs62485838","clinical_significance":[],"strand":1,"feature_type":"variation","end":140580330,"alleles":["T","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580330,"source":"dbSNP"},{"alleles":["-","GTATGCATGTATGC"],"end":140580330,"strand":1,"feature_type":"variation","start":140580331,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1360581084","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1021115635","feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140580332,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580332},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140580333,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580333,"clinical_significance":[],"seq_region_name":"7","id":"rs79516429"},{"seq_region_name":"7","id":"rs1563155730","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580334,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["-","CATGTATGTATT"],"end":140580333},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580334,"source":"dbSNP","strand":1,"feature_type":"variation","end":140580334,"alleles":["T","C"],"seq_region_name":"7","id":"rs1798490106","clinical_significance":[]},{"seq_region_name":"7","id":"rs1364255707","clinical_significance":[],"strand":1,"feature_type":"variation","end":140580346,"alleles":["TATTTATTTATTT","TATTTATTT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580334,"source":"dbSNP"},{"end":140580337,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140580337,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs536277793","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1259340074","source":"dbSNP","start":140580338,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140580338,"feature_type":"variation","strand":1},{"start":140580341,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140580341,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798490832","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130630534","feature_type":"variation","strand":1,"end":140580348,"alleles":["TTTTT","TTTT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580344},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140580345,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580345,"source":"dbSNP","seq_region_name":"7","id":"rs1046968049","clinical_significance":[]},{"alleles":["GG","-"],"end":140580350,"strand":1,"feature_type":"variation","start":140580349,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798491219","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798491391","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580356,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140580356},{"start":140580360,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G","T"],"end":140580360,"strand":1,"feature_type":"variation","id":"rs1035200245","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140580361,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580361,"clinical_significance":[],"seq_region_name":"7","id":"rs959044068"},{"clinical_significance":[],"id":"rs1798491992","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140580362,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580362},{"end":140580364,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140580364,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798492164"},{"feature_type":"variation","strand":1,"end":140580365,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580365,"clinical_significance":[],"seq_region_name":"7","id":"rs890962748"},{"seq_region_name":"7","id":"rs1490914096","clinical_significance":[],"start":140580366,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G","T"],"end":140580366,"strand":1,"feature_type":"variation"},{"start":140580368,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140580368,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585680903","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580369,"feature_type":"variation","strand":1,"end":140580369,"alleles":["G","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs556688031"},{"seq_region_name":"7","id":"rs1209377483","clinical_significance":[],"start":140580371,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140580371,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"id":"rs1798493335","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580375,"source":"dbSNP","strand":1,"feature_type":"variation","end":140580375,"alleles":["T","A"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580378,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140580378,"clinical_significance":[],"seq_region_name":"7","id":"rs1585680934"},{"clinical_significance":[],"id":"rs554244806","seq_region_name":"7","source":"dbSNP","start":140580379,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140580379,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563155754","alleles":["C","T"],"end":140580380,"feature_type":"variation","strand":1,"source":"dbSNP","start":140580380,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs374430866","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580386,"feature_type":"variation","strand":1,"end":140580386,"alleles":["A","T"]},{"seq_region_name":"7","id":"rs2130630667","clinical_significance":[],"start":140580395,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140580395,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580398,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140580398,"clinical_significance":[],"seq_region_name":"7","id":"rs1205229617"},{"seq_region_name":"7","id":"rs1798494442","clinical_significance":[],"start":140580399,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140580399,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798494606","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580406,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140580406},{"start":140580408,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","T"],"end":140580408,"strand":1,"feature_type":"variation","id":"rs191322892","seq_region_name":"7","clinical_significance":[]},{"start":140580410,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140580410,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs951813979","clinical_significance":[]},{"source":"dbSNP","start":140580416,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140580416,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1563155768"},{"strand":1,"feature_type":"variation","end":140580421,"alleles":["G","C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580421,"source":"dbSNP","seq_region_name":"7","id":"rs1284382083","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580427,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140580427,"clinical_significance":[],"id":"rs752327583","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580433,"feature_type":"variation","strand":1,"end":140580433,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1021565884"},{"end":140580436,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140580436,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798495533","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580438,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140580438,"clinical_significance":[],"seq_region_name":"7","id":"rs1798495703"},{"seq_region_name":"7","id":"rs1178230977","clinical_significance":[],"end":140580439,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140580439,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580440,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140580440,"id":"rs2429996","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140580444,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580444,"clinical_significance":[],"id":"rs944506448","seq_region_name":"7"},{"end":140580445,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140580445,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1446220777","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1040330682","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580447,"feature_type":"variation","strand":1,"end":140580447,"alleles":["G","A"]},{"source":"dbSNP","start":140580454,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140580454,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1798496698","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798496795","end":140580455,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140580455,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580460,"feature_type":"variation","strand":1,"end":140580460,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1798496907"},{"alleles":["A","G"],"end":140580461,"feature_type":"variation","strand":1,"source":"dbSNP","start":140580461,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1181586770","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1176976538","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580462,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140580462},{"feature_type":"variation","strand":1,"end":140580463,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580463,"clinical_significance":[],"id":"rs1412904473","seq_region_name":"7"},{"seq_region_name":"7","id":"rs2130630847","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580464,"source":"dbSNP","strand":1,"feature_type":"variation","end":140580464,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1481534570","clinical_significance":[],"start":140580470,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140580470,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs543105549","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580473,"feature_type":"variation","strand":1,"end":140580473,"alleles":["C","A"]},{"source":"dbSNP","start":140580476,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140580476,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs928682814"},{"id":"rs1447612548","seq_region_name":"7","clinical_significance":[],"end":140580477,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140580477,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580478,"feature_type":"variation","strand":1,"end":140580478,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs921825169"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1207359920","feature_type":"variation","strand":1,"end":140580485,"alleles":["CTATCTA","CTA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580479},{"clinical_significance":[],"seq_region_name":"7","id":"rs992039379","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140580482,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580482},{"start":140580483,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140580483,"strand":1,"feature_type":"variation","id":"rs1352239044","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs561215991","clinical_significance":[],"alleles":["A","G"],"end":140580486,"strand":1,"feature_type":"variation","start":140580486,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs76134176","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580489,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140580489},{"end":140580499,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140580499,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs916184584","clinical_significance":[]},{"source":"dbSNP","start":140580501,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140580501,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs2130630933","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1798498992","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140580503,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580503,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140580505,"alleles":["A","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580505,"source":"dbSNP","seq_region_name":"7","id":"rs932663182","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580508,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","-"],"end":140580508,"seq_region_name":"7","id":"rs763978496","clinical_significance":[]},{"id":"rs1798499255","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140580508,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580508,"source":"dbSNP"},{"seq_region_name":"7","id":"rs114641713","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580509,"source":"dbSNP","strand":1,"feature_type":"variation","end":140580509,"alleles":["G","A"]},{"end":140580510,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140580510,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798499600","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1232107819","source":"dbSNP","start":140580518,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140580518,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140580519,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140580519,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs183817786"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1299227954","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140580535,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580535},{"clinical_significance":[],"seq_region_name":"7","id":"rs1432807914","source":"dbSNP","start":140580536,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140580536,"alleles":["T","C","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798500096","alleles":["C","G"],"end":140580537,"feature_type":"variation","strand":1,"source":"dbSNP","start":140580537,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798500193","source":"dbSNP","start":140580539,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140580539,"alleles":["T","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1798500298","seq_region_name":"7","end":140580546,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140580546,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140580550,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140580550,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1337326848"},{"seq_region_name":"7","id":"rs1282798714","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140580559,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580559,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1798500662","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580564,"source":"dbSNP","strand":1,"feature_type":"variation","end":140580564,"alleles":["C","A"]},{"seq_region_name":"7","id":"rs1010990598","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580568,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140580568},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798500901","alleles":["C","T"],"end":140580569,"feature_type":"variation","strand":1,"source":"dbSNP","start":140580569,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","T"],"end":140580574,"strand":1,"feature_type":"variation","start":140580574,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798501022","clinical_significance":[]},{"alleles":["T","C"],"end":140580575,"strand":1,"feature_type":"variation","start":140580575,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1379026351","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1172161839","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580577,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140580577},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580586,"feature_type":"variation","strand":1,"end":140580586,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1798501398"},{"clinical_significance":[],"id":"rs1798501495","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580588,"feature_type":"variation","strand":1,"end":140580588,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130631090","alleles":["G","T"],"end":140580590,"feature_type":"variation","strand":1,"source":"dbSNP","start":140580590,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140580593,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580593,"source":"dbSNP","id":"rs565039384","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1298435330","source":"dbSNP","start":140580595,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140580595,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs902687537","clinical_significance":[],"end":140580596,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140580596,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140580597,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580597,"clinical_significance":[],"id":"rs1798501916","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140580598,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580598,"source":"dbSNP","id":"rs1798502026","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1798502126","seq_region_name":"7","source":"dbSNP","start":140580601,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140580601,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580604,"feature_type":"variation","strand":1,"end":140580604,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1186825385"},{"seq_region_name":"7","id":"rs2130631153","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140580605,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580605,"source":"dbSNP"},{"source":"dbSNP","start":140580607,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140580607,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs564747550","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1798502342","clinical_significance":[],"start":140580608,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140580608,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580609,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140580609,"seq_region_name":"7","id":"rs532520897","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798502568","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580610,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140580610},{"alleles":["C","T"],"end":140580613,"feature_type":"variation","strand":1,"source":"dbSNP","start":140580613,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1035253215"},{"start":140580614,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140580614,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798502794","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580615,"feature_type":"variation","strand":1,"end":140580615,"alleles":["C","T"],"clinical_significance":[],"id":"rs929754185","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140580617,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580617,"clinical_significance":[],"seq_region_name":"7","id":"rs1206160903"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580618,"source":"dbSNP","strand":1,"feature_type":"variation","end":140580618,"alleles":["C","A"],"id":"rs1798503115","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140580621,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140580621,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs551011754","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798503320","feature_type":"variation","strand":1,"alleles":["T","A"],"end":140580626,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580626},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798503429","feature_type":"variation","strand":1,"end":140580629,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580629},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563155896","source":"dbSNP","start":140580630,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140580630,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["TATTATTATTATT","TATTATTATTATTATT"],"end":140580643,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580631,"source":"dbSNP","seq_region_name":"7","id":"rs1798503662","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1278424073","alleles":["T","C"],"end":140580634,"feature_type":"variation","strand":1,"source":"dbSNP","start":140580634,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140580635,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140580635,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs2130631271","seq_region_name":"7"},{"id":"rs1798503881","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580637,"source":"dbSNP","strand":1,"feature_type":"variation","end":140580636,"alleles":["-","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1263974875","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580641,"feature_type":"variation","strand":1,"end":140580641,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs1798504092","clinical_significance":[],"end":140580643,"alleles":["TT","TTGTT"],"strand":1,"feature_type":"variation","start":140580642,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798504225","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140580643,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580643},{"source":"dbSNP","start":140580644,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A","C"],"end":140580644,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1339741343"},{"source":"dbSNP","start":140580645,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140580645,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798504467"},{"clinical_significance":[],"id":"rs1276140316","seq_region_name":"7","end":140580657,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140580657,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1462836670","seq_region_name":"7","source":"dbSNP","start":140580661,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140580661,"alleles":["G","T"],"feature_type":"variation","strand":1},{"alleles":["G","A"],"end":140580663,"strand":1,"feature_type":"variation","start":140580663,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1225473903","clinical_significance":[]},{"seq_region_name":"7","id":"rs1363833479","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580664,"source":"dbSNP","strand":1,"feature_type":"variation","end":140580664,"alleles":["T","G"]},{"start":140580668,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140580668,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1201468837","clinical_significance":[]},{"seq_region_name":"7","id":"rs1315596282","clinical_significance":[],"start":140580669,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140580669,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"end":140580670,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140580670,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798505254"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580672,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140580672,"clinical_significance":[],"id":"rs1450151243","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1236705758","alleles":["G","A"],"end":140580673,"feature_type":"variation","strand":1,"source":"dbSNP","start":140580673,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580677,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140580677,"seq_region_name":"7","id":"rs1798505550","clinical_significance":[]},{"seq_region_name":"7","id":"rs1338461805","clinical_significance":[],"start":140580686,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C","T"],"end":140580686,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140580688,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140580688,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1046851977"},{"seq_region_name":"7","id":"rs1798505909","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580689,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140580689},{"seq_region_name":"7","id":"rs1372699158","clinical_significance":[],"strand":1,"feature_type":"variation","end":140580691,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580691,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1798506109","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140580692,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580692,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580695,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140580695,"clinical_significance":[],"seq_region_name":"7","id":"rs147440159"},{"clinical_significance":[],"seq_region_name":"7","id":"rs368985943","end":140580696,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140580696,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1798506529","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580697,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140580697},{"source":"dbSNP","start":140580699,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140580699,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1385971443"},{"source":"dbSNP","start":140580699,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140580705,"alleles":["CAATCTC","CAATCTCCAATCTC"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130631476"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580700,"source":"dbSNP","strand":1,"feature_type":"variation","end":140580700,"alleles":["A","C"],"seq_region_name":"7","id":"rs1027312667","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580703,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140580703,"clinical_significance":[],"seq_region_name":"7","id":"rs1472121106"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580704,"source":"dbSNP","strand":1,"feature_type":"variation","end":140580704,"alleles":["T","C"],"id":"rs1798506842","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580705,"source":"dbSNP","strand":1,"feature_type":"variation","end":140580705,"alleles":["C","T"],"seq_region_name":"7","id":"rs2130631511","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798506951","feature_type":"variation","strand":1,"end":140580709,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580709},{"source":"dbSNP","start":140580717,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140580717,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1585681567","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1798507179","clinical_significance":[],"start":140580718,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140580718,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798507270","end":140580719,"alleles":["CC","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140580718,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","A"],"end":140580719,"strand":1,"feature_type":"variation","start":140580719,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798507373","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140580721,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580721,"source":"dbSNP","id":"rs1798507470","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1237261495","clinical_significance":[],"end":140580722,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140580722,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580723,"source":"dbSNP","strand":1,"feature_type":"variation","end":140580723,"alleles":["G","A","T"],"seq_region_name":"7","id":"rs951926228","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140580724,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580724,"clinical_significance":[],"seq_region_name":"7","id":"rs1798507762"},{"seq_region_name":"7","id":"rs1176540670","clinical_significance":[],"start":140580728,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140580728,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140580732,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580732,"source":"dbSNP","seq_region_name":"7","id":"rs780943765","clinical_significance":[]},{"alleles":["A","G"],"end":140580737,"strand":1,"feature_type":"variation","start":140580737,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1202625885","clinical_significance":[]},{"seq_region_name":"7","id":"rs1340780564","clinical_significance":[],"strand":1,"feature_type":"variation","end":140580742,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580742,"source":"dbSNP"},{"end":140580746,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140580746,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798508328"},{"end":140580750,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140580750,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1291930819","clinical_significance":[]},{"alleles":["A","G"],"end":140580754,"strand":1,"feature_type":"variation","start":140580754,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798508534","clinical_significance":[]},{"id":"rs1798508648","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140580760,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580760,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1015060843","seq_region_name":"7","end":140580764,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140580764,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140580772,"alleles":["GGG","GGGG"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580770,"clinical_significance":[],"seq_region_name":"7","id":"rs1798508872"},{"source":"dbSNP","start":140580771,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140580771,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs965926723"},{"seq_region_name":"7","id":"rs1229928901","clinical_significance":[],"start":140580774,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140580774,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs189998022","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580777,"feature_type":"variation","strand":1,"end":140580777,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1332546558","clinical_significance":[],"strand":1,"feature_type":"variation","end":140580779,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580779,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140580781,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580781,"source":"dbSNP","seq_region_name":"7","id":"rs1239173908","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140580782,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580782,"clinical_significance":[],"seq_region_name":"7","id":"rs181670804"},{"seq_region_name":"7","id":"rs1431977289","clinical_significance":[],"end":140580784,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140580784,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140580789,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140580789,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs749416522","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1798509961","clinical_significance":[],"alleles":["T","C"],"end":140580791,"strand":1,"feature_type":"variation","start":140580791,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140580793,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140580793,"strand":1,"feature_type":"variation","id":"rs1442590245","seq_region_name":"7","clinical_significance":[]},{"id":"rs931879398","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140580798,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580798,"source":"dbSNP"},{"start":140580805,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140580805,"alleles":["T","A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs527942498","clinical_significance":[]},{"source":"dbSNP","start":140580807,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140580807,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1306358461"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580810,"source":"dbSNP","strand":1,"feature_type":"variation","end":140580810,"alleles":["C","A","T"],"id":"rs985499679","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585681772","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580817,"feature_type":"variation","strand":1,"end":140580817,"alleles":["A","G"]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140580821,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580821,"source":"dbSNP","seq_region_name":"7","id":"rs1798510673","clinical_significance":[]},{"source":"dbSNP","start":140580823,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140580823,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1409501208"},{"start":140580824,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140580824,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs552374020","clinical_significance":[]},{"source":"dbSNP","start":140580825,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140580825,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs570976818"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140580826,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580826,"source":"dbSNP","id":"rs1339166803","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1798511116","seq_region_name":"7","end":140580828,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140580828,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1798511224","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580829,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140580829},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580830,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140580830,"clinical_significance":[],"seq_region_name":"7","id":"rs1585681815"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580832,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TCA","-"],"end":140580834,"seq_region_name":"7","id":"rs1798511423","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1039923324","end":140580837,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140580837,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585681838","source":"dbSNP","start":140580838,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140580838,"alleles":["T","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs899774359","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580839,"feature_type":"variation","strand":1,"end":140580839,"alleles":["G","A","T"]},{"source":"dbSNP","start":140580844,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140580844,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798511868"},{"id":"rs1798512034","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140580846,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580846,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140580847,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580847,"clinical_significance":[],"id":"rs1798512165","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140580849,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580849,"clinical_significance":[],"seq_region_name":"7","id":"rs111888492"},{"seq_region_name":"7","id":"rs1042488883","clinical_significance":[],"end":140580852,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","start":140580852,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140580854,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140580854,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798512596","clinical_significance":[]},{"clinical_significance":[],"id":"rs902572168","seq_region_name":"7","end":140580856,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140580856,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798512816","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580857,"feature_type":"variation","strand":1,"end":140580857,"alleles":["G","A"]},{"end":140580859,"alleles":["A","G","T"],"strand":1,"feature_type":"variation","start":140580859,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1250090526","seq_region_name":"7","clinical_significance":[]},{"start":140580860,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140580860,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1179541291","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130631940","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580866,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140580866},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580867,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140580867,"seq_region_name":"7","id":"rs1021619467","clinical_significance":[]},{"clinical_significance":[],"id":"rs190065886","seq_region_name":"7","source":"dbSNP","start":140580873,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140580873,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1798513489","clinical_significance":[],"start":140580874,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140580874,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140580877,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580877,"source":"dbSNP","seq_region_name":"7","id":"rs1217666545","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1268969250","feature_type":"variation","strand":1,"end":140580878,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580878},{"source":"dbSNP","start":140580879,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140580879,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1223199939"},{"clinical_significance":[],"id":"rs1798514396","seq_region_name":"7","source":"dbSNP","start":140580881,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140580881,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140580888,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140580888,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1449388944"},{"seq_region_name":"7","id":"rs1288970551","clinical_significance":[],"start":140580890,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140580890,"strand":1,"feature_type":"variation"},{"start":140580893,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140580893,"strand":1,"feature_type":"variation","id":"rs1224296691","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130632018","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140580894,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580894,"source":"dbSNP"},{"clinical_significance":[],"id":"rs112166921","seq_region_name":"7","source":"dbSNP","start":140580900,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140580900,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1798515303","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580902,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140580902},{"seq_region_name":"7","id":"rs1286275262","clinical_significance":[],"end":140580904,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140580904,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1798515648","clinical_significance":[],"start":140580907,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140580907,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140580912,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","CC"],"end":140580912,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1228014807","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1346454287","clinical_significance":[],"alleles":["C","G","T"],"end":140580912,"strand":1,"feature_type":"variation","start":140580912,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1798516161","clinical_significance":[],"end":140580920,"alleles":["TGA","-"],"strand":1,"feature_type":"variation","start":140580918,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs2130632076","clinical_significance":[],"start":140580922,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140580922,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1798516255","clinical_significance":[],"start":140580922,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["CC","C"],"end":140580923,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580924,"source":"dbSNP","strand":1,"feature_type":"variation","end":140580924,"alleles":["A","T"],"seq_region_name":"7","id":"rs1798516366","clinical_significance":[]},{"alleles":["T","G"],"end":140580926,"strand":1,"feature_type":"variation","start":140580926,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1035750553","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580930,"source":"dbSNP","strand":1,"feature_type":"variation","end":140580930,"alleles":["C","A"],"id":"rs1798516571","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1434314628","feature_type":"variation","strand":1,"end":140580931,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580931},{"seq_region_name":"7","id":"rs960377106","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140580932,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580932,"source":"dbSNP"},{"id":"rs748258744","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580933,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140580933},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580935,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140580935,"clinical_significance":[],"id":"rs1459326980","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140580939,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580939,"source":"dbSNP","id":"rs1798517111","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","A"],"end":140580942,"feature_type":"variation","strand":1,"source":"dbSNP","start":140580942,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798517240"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798517336","feature_type":"variation","strand":1,"end":140580945,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580945},{"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140580954,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580954,"clinical_significance":[],"seq_region_name":"7","id":"rs1798517450"},{"source":"dbSNP","start":140580961,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140580961,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1012448606"},{"end":140580962,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140580962,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs181818799","clinical_significance":[]},{"seq_region_name":"7","id":"rs887466182","clinical_significance":[],"start":140580963,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140580963,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"start":140580968,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G","T"],"end":140580968,"strand":1,"feature_type":"variation","id":"rs1004934537","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs62485839","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","G"],"end":140580971,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580971,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs112639545","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580976,"feature_type":"variation","strand":1,"end":140580976,"alleles":["G","C"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580977,"feature_type":"variation","strand":1,"end":140580977,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1046738798"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798518416","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140580988,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140580988},{"clinical_significance":[],"id":"rs1466254389","seq_region_name":"7","source":"dbSNP","start":140580989,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140580989,"feature_type":"variation","strand":1},{"end":140580990,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140580990,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1479196646"},{"end":140580991,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140580991,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1798518742","seq_region_name":"7"},{"alleles":["G","T"],"end":140580992,"feature_type":"variation","strand":1,"source":"dbSNP","start":140580992,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798518836"},{"strand":1,"feature_type":"variation","end":140580996,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140580996,"source":"dbSNP","seq_region_name":"7","id":"rs1207816669","clinical_significance":[]},{"id":"rs2429997","seq_region_name":"7","clinical_significance":[],"start":140580998,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140580998,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581000,"feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140581000,"clinical_significance":[],"seq_region_name":"7","id":"rs186465522"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798519323","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581007,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140581007},{"end":140581009,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140581009,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1798519423","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140581014,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140581014,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1798519519","seq_region_name":"7"},{"alleles":["C","T"],"end":140581017,"feature_type":"variation","strand":1,"source":"dbSNP","start":140581017,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798519653"},{"seq_region_name":"7","id":"rs1798519742","clinical_significance":[],"strand":1,"feature_type":"variation","end":140581030,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581030,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581031,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140581031,"id":"rs1401636238","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581032,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140581032,"clinical_significance":[],"id":"rs1039571649","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1320707818","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581034,"source":"dbSNP","strand":1,"feature_type":"variation","end":140581036,"alleles":["GGG","GG"]},{"seq_region_name":"7","id":"rs1270887097","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581037,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140581037},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581038,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140581038,"clinical_significance":[],"seq_region_name":"7","id":"rs189657426"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140581039,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581039,"source":"dbSNP","seq_region_name":"7","id":"rs1798520391","clinical_significance":[]},{"seq_region_name":"7","id":"rs1359110308","clinical_significance":[],"start":140581042,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140581042,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581043,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140581043,"seq_region_name":"7","id":"rs1482741733","clinical_significance":[]},{"clinical_significance":[],"id":"rs187921","seq_region_name":"7","feature_type":"variation","strand":1,"end":140581045,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581045},{"end":140581049,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140581049,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs953153656","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1470467908","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581053,"feature_type":"variation","strand":1,"end":140581053,"alleles":["A","G"]},{"start":140581060,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140581060,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs544073410","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs563025607","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581061,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140581061},{"end":140581063,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140581063,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1171076407","seq_region_name":"7"},{"start":140581066,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140581066,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798521427","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1347437581","end":140581070,"alleles":["CC","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140581069,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140581073,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581073,"source":"dbSNP","seq_region_name":"7","id":"rs1402222641","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798521749","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140581074,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581074,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140581076,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581076,"source":"dbSNP","seq_region_name":"7","id":"rs1798521859","clinical_significance":[]},{"start":140581079,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140581079,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1423855629","clinical_significance":[]},{"alleles":["T","C"],"end":140581080,"strand":1,"feature_type":"variation","start":140581080,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1434489188","clinical_significance":[]},{"id":"rs1798522147","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581082,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140581082},{"strand":1,"feature_type":"variation","end":140581083,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581083,"source":"dbSNP","seq_region_name":"7","id":"rs1798522251","clinical_significance":[]},{"end":140581087,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140581087,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1798522379","seq_region_name":"7","clinical_significance":[]},{"end":140581089,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140581089,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1450809232","seq_region_name":"7"},{"end":140581099,"alleles":["C","-"],"strand":1,"feature_type":"variation","start":140581099,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1351693267","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140581100,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581100,"source":"dbSNP","seq_region_name":"7","id":"rs1187888880","clinical_significance":[]},{"seq_region_name":"7","id":"rs1042960464","clinical_significance":[],"strand":1,"feature_type":"variation","end":140581101,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581101,"source":"dbSNP"},{"id":"rs1798522914","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581105,"source":"dbSNP","strand":1,"feature_type":"variation","end":140581105,"alleles":["A","C"]},{"start":140581106,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140581106,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs144236182","clinical_significance":[]},{"id":"rs1208240879","seq_region_name":"7","clinical_significance":[],"start":140581108,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140581108,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140581109,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140581109,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs978479745"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140581110,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581110,"source":"dbSNP","seq_region_name":"7","id":"rs1275426775","clinical_significance":[]},{"id":"rs1230624463","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581111,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140581111},{"start":140581116,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140581116,"alleles":["A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1035637846","clinical_significance":[]},{"end":140581122,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140581122,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs924075588"},{"end":140581123,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140581123,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs181062403","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140581125,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581125,"source":"dbSNP","seq_region_name":"7","id":"rs939428445","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140581126,"alleles":["A","C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581126,"clinical_significance":[],"seq_region_name":"7","id":"rs1585682438"},{"seq_region_name":"7","id":"rs1798524187","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581131,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140581131},{"alleles":["G","A","T"],"end":140581132,"feature_type":"variation","strand":1,"source":"dbSNP","start":140581132,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs560085184"},{"seq_region_name":"7","id":"rs1358157936","clinical_significance":[],"alleles":["CCTGTGCC","C"],"end":140581140,"strand":1,"feature_type":"variation","start":140581133,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1798524554","seq_region_name":"7","feature_type":"variation","strand":1,"end":140581135,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581135},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581136,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140581136,"id":"rs1168843421","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140581138,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581138,"source":"dbSNP","id":"rs1431064068","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140581139,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581139,"source":"dbSNP","seq_region_name":"7","id":"rs1798524868","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1387808428","feature_type":"variation","strand":1,"end":140581142,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581142},{"id":"rs1023175168","seq_region_name":"7","clinical_significance":[],"start":140581147,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140581147,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs116596233","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140581148,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581148},{"end":140581151,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140581151,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1258005966","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1179957615","alleles":["C","A","T"],"end":140581152,"feature_type":"variation","strand":1,"source":"dbSNP","start":140581152,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581155,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140581155,"clinical_significance":[],"seq_region_name":"7","id":"rs775445121"},{"seq_region_name":"7","id":"rs746997038","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581156,"source":"dbSNP","strand":1,"feature_type":"variation","end":140581156,"alleles":["T","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585682550","alleles":["T","G"],"end":140581164,"feature_type":"variation","strand":1,"source":"dbSNP","start":140581164,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140581170,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140581170,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1252723056","clinical_significance":[]},{"end":140581171,"alleles":["T","A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140581171,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1563156192"},{"seq_region_name":"7","id":"rs1798526096","clinical_significance":[],"start":140581185,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140581185,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1207595900","source":"dbSNP","start":140581186,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140581186,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581192,"source":"dbSNP","strand":1,"feature_type":"variation","end":140581192,"alleles":["A","G","T"],"seq_region_name":"7","id":"rs1798526291","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581193,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140581193,"seq_region_name":"7","id":"rs1798526424","clinical_significance":[]},{"id":"rs1340075990","seq_region_name":"7","clinical_significance":[],"end":140581194,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140581194,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585682575","end":140581195,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140581195,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1798526759","seq_region_name":"7","source":"dbSNP","start":140581196,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140581196,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1026582313","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140581197,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581197},{"end":140581199,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140581199,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1470961051"},{"clinical_significance":[],"id":"rs1585682597","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140581201,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581201},{"clinical_significance":[],"id":"rs1049338852","seq_region_name":"7","source":"dbSNP","start":140581205,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140581205,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140581215,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581215,"source":"dbSNP","id":"rs2130632808","seq_region_name":"7","clinical_significance":[]},{"start":140581217,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140581217,"strand":1,"feature_type":"variation","id":"rs1798527309","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","A","G","T"],"end":140581218,"feature_type":"variation","strand":1,"source":"dbSNP","start":140581218,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs198865","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1378830654","clinical_significance":[],"alleles":["G","A","C"],"end":140581219,"strand":1,"feature_type":"variation","start":140581219,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798527785","end":140581220,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140581220,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1308209411","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140581222,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581222,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1798528016","clinical_significance":[],"end":140581224,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140581224,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1798528134","clinical_significance":[],"alleles":["C","T"],"end":140581225,"strand":1,"feature_type":"variation","start":140581225,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140581228,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581228,"clinical_significance":[],"seq_region_name":"7","id":"rs1798528255"},{"seq_region_name":"7","id":"rs1004583506","clinical_significance":[],"start":140581230,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140581230,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs571049461","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581233,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140581233},{"start":140581239,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140581239,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1419524415","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1167486698","end":140581240,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140581240,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798529108","feature_type":"variation","strand":1,"end":140581242,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581242},{"source":"dbSNP","start":140581244,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140581244,"alleles":["A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798529275"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140581247,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581247,"clinical_significance":[],"id":"rs982470570","seq_region_name":"7"},{"seq_region_name":"7","id":"rs531982503","clinical_significance":[],"strand":1,"feature_type":"variation","end":140581249,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581249,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1036430855","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581252,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140581252},{"seq_region_name":"7","id":"rs1162599332","clinical_significance":[],"start":140581254,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140581254,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1385096907","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581259,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140581259},{"clinical_significance":[],"seq_region_name":"7","id":"rs943839609","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581263,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140581263},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140581264,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581264,"source":"dbSNP","seq_region_name":"7","id":"rs1482236220","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs151202396","feature_type":"variation","strand":1,"alleles":["AAAAGAAAAGAAAAGAAA","AAAAGAAAAGAAA","AAAAGAAAAGAAAAGAAAAGAAA"],"end":140581281,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581264},{"source":"dbSNP","start":140581265,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140581265,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1251158677"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798530547","feature_type":"variation","strand":1,"end":140581277,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581277},{"clinical_significance":[],"seq_region_name":"7","id":"rs975570431","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581278,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140581278},{"id":"rs1798530756","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140581281,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581281,"source":"dbSNP"},{"seq_region_name":"7","id":"rs901632906","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581282,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140581282},{"seq_region_name":"7","id":"rs1798530971","clinical_significance":[],"strand":1,"feature_type":"variation","end":140581283,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581283,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798531074","alleles":["G","A"],"end":140581284,"feature_type":"variation","strand":1,"source":"dbSNP","start":140581284,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1798531165","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581291,"feature_type":"variation","strand":1,"end":140581291,"alleles":["A","C"]},{"seq_region_name":"7","id":"rs947234772","clinical_significance":[],"start":140581294,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G","T"],"end":140581294,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs879386258","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581295,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140581295},{"end":140581296,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140581296,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798531490","clinical_significance":[]},{"clinical_significance":[],"id":"rs1798531590","seq_region_name":"7","source":"dbSNP","start":140581302,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140581302,"alleles":["G","A"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140581303,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581303,"source":"dbSNP","seq_region_name":"7","id":"rs1798531713","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140581309,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581309,"source":"dbSNP","id":"rs1798531877","seq_region_name":"7","clinical_significance":[]},{"id":"rs58041326","seq_region_name":"7","clinical_significance":[],"alleles":["A","G"],"end":140581310,"strand":1,"feature_type":"variation","start":140581310,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1798532222","seq_region_name":"7","end":140581311,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140581311,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585682797","feature_type":"variation","strand":1,"end":140581314,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581314},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581315,"feature_type":"variation","strand":1,"end":140581315,"alleles":["T","C"],"clinical_significance":[],"id":"rs2130633104","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1798532534","seq_region_name":"7","source":"dbSNP","start":140581317,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140581317,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140581320,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140581320,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798532693"},{"clinical_significance":[],"id":"rs1290639736","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581322,"feature_type":"variation","strand":1,"end":140581322,"alleles":["C","A"]},{"clinical_significance":[],"id":"rs1798532999","seq_region_name":"7","feature_type":"variation","strand":1,"end":140581325,"alleles":["GG","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581324},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581328,"source":"dbSNP","strand":1,"feature_type":"variation","end":140581328,"alleles":["C","T"],"seq_region_name":"7","id":"rs1798533173","clinical_significance":[]},{"alleles":["T","C"],"end":140581329,"strand":1,"feature_type":"variation","start":140581329,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs953204732","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798533442","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140581330,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581330},{"start":140581336,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140581336,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1348303194","clinical_significance":[]},{"source":"dbSNP","start":140581339,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140581339,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1327783413"},{"seq_region_name":"7","id":"rs568968465","clinical_significance":[],"start":140581340,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140581340,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1798533939","clinical_significance":[],"start":140581343,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["CAGCAGCAGCAGCA","CAGCAGCAGCAGCAGCA"],"end":140581356,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1276701081","clinical_significance":[],"end":140581344,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140581344,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798534288","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581346,"feature_type":"variation","strand":1,"end":140581346,"alleles":["C","G","T"]},{"source":"dbSNP","start":140581347,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140581347,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs934566472"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581349,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140581349,"clinical_significance":[],"seq_region_name":"7","id":"rs2130633208"},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140581358,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581358,"source":"dbSNP","seq_region_name":"7","id":"rs1354179258","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798534819","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581361,"feature_type":"variation","strand":1,"end":140581361,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1011800373","clinical_significance":[],"start":140581363,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140581363,"strand":1,"feature_type":"variation"},{"id":"rs186320351","seq_region_name":"7","clinical_significance":[],"start":140581364,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140581364,"alleles":["G","A","T"],"strand":1,"feature_type":"variation"},{"end":140581365,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140581365,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs554628534"},{"alleles":["A","G"],"end":140581366,"strand":1,"feature_type":"variation","start":140581366,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798535575","clinical_significance":[]},{"end":140581370,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140581370,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs2130633264","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581372,"source":"dbSNP","strand":1,"feature_type":"variation","end":140581372,"alleles":["A","C","G"],"seq_region_name":"7","id":"rs566430090","clinical_significance":[]},{"end":140581374,"alleles":["A","C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140581374,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1389100497"},{"end":140581380,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140581380,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1439143295"},{"clinical_significance":[],"seq_region_name":"7","id":"rs772490455","source":"dbSNP","start":140581381,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140581381,"alleles":["C","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs978151723","source":"dbSNP","start":140581383,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140581383,"alleles":["T","C"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140581386,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140581386,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1471497438"},{"clinical_significance":[],"id":"rs1798536493","seq_region_name":"7","source":"dbSNP","start":140581387,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140581387,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs776499974","feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140581392,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581392},{"id":"rs1798536751","seq_region_name":"7","clinical_significance":[],"end":140581393,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140581393,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1798536841","clinical_significance":[],"alleles":["G","A"],"end":140581394,"strand":1,"feature_type":"variation","start":140581394,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140581402,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581402,"clinical_significance":[],"seq_region_name":"7","id":"rs1798536941"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140581404,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581404,"source":"dbSNP","seq_region_name":"7","id":"rs923940423","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140581409,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581409,"source":"dbSNP","seq_region_name":"7","id":"rs1798537184","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140581418,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581418,"source":"dbSNP","seq_region_name":"7","id":"rs533759935","clinical_significance":[]},{"start":140581419,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","T"],"end":140581419,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1023480927","clinical_significance":[]},{"start":140581420,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140581420,"strand":1,"feature_type":"variation","id":"rs773534573","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581423,"feature_type":"variation","strand":1,"end":140581423,"alleles":["T","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1798537701"},{"start":140581428,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140581428,"strand":1,"feature_type":"variation","id":"rs960655044","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581431,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140581431,"clinical_significance":[],"seq_region_name":"7","id":"rs747563344"},{"source":"dbSNP","start":140581432,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140581432,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798538023"},{"start":140581434,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140581434,"alleles":["G","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585683070","clinical_significance":[]},{"seq_region_name":"7","id":"rs1270399563","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581436,"source":"dbSNP","strand":1,"feature_type":"variation","end":140581436,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1184608921","source":"dbSNP","start":140581436,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140581442,"alleles":["GACCCGA","GA"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1387560101","clinical_significance":[],"start":140581437,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140581437,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs771488725","source":"dbSNP","start":140581440,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140581440,"alleles":["C","G","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1278546544","feature_type":"variation","strand":1,"end":140581441,"alleles":["G","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581441},{"seq_region_name":"7","id":"rs1798538884","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581447,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140581447},{"alleles":["C","G"],"end":140581451,"feature_type":"variation","strand":1,"source":"dbSNP","start":140581451,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1162692588","seq_region_name":"7"},{"seq_region_name":"7","id":"rs2130633470","clinical_significance":[],"start":140581452,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140581452,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140581453,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140581453,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130633481"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1397279090","source":"dbSNP","start":140581454,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140581454,"alleles":["T","A","C"],"feature_type":"variation","strand":1},{"start":140581462,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140581462,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798539236","clinical_significance":[]},{"clinical_significance":[],"id":"rs1798539351","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140581467,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581467},{"clinical_significance":[],"id":"rs1411763290","seq_region_name":"7","end":140581468,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140581468,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs916641762","seq_region_name":"7","clinical_significance":[],"end":140581476,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140581476,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs950977342","source":"dbSNP","start":140581485,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140581485,"alleles":["C","T"],"feature_type":"variation","strand":1},{"id":"rs558857665","seq_region_name":"7","clinical_significance":[],"start":140581493,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140581493,"alleles":["C","A","T"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581495,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140581495,"seq_region_name":"7","id":"rs1399910945","clinical_significance":[]},{"clinical_significance":[],"id":"rs1455408075","seq_region_name":"7","source":"dbSNP","start":140581498,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140581498,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140581499,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140581499,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798540192"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581507,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140581507,"clinical_significance":[],"id":"rs114089537","seq_region_name":"7"},{"start":140581508,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140581508,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798540381","clinical_significance":[]},{"source":"dbSNP","start":140581508,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["GGGGG","GGGG"],"end":140581512,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798540522"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140581509,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581509,"clinical_significance":[],"seq_region_name":"7","id":"rs1798540616"},{"seq_region_name":"7","id":"rs1585683219","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581511,"source":"dbSNP","strand":1,"feature_type":"variation","end":140581511,"alleles":["G","T"]},{"seq_region_name":"7","id":"rs1585683225","clinical_significance":[],"alleles":["G","T"],"end":140581515,"strand":1,"feature_type":"variation","start":140581515,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581516,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140581516,"seq_region_name":"7","id":"rs1798540900","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798540995","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581518,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140581518},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585683230","source":"dbSNP","start":140581521,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140581521,"alleles":["T","G"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140581525,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581525,"source":"dbSNP","seq_region_name":"7","id":"rs965424365","clinical_significance":[]},{"alleles":["G","T"],"end":140581527,"feature_type":"variation","strand":1,"source":"dbSNP","start":140581527,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585683248"},{"clinical_significance":[],"id":"rs1798541361","seq_region_name":"7","end":140581528,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140581528,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1798541463","clinical_significance":[],"alleles":["C","T"],"end":140581534,"strand":1,"feature_type":"variation","start":140581534,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["C","T"],"end":140581535,"feature_type":"variation","strand":1,"source":"dbSNP","start":140581535,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798541636"},{"start":140581538,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140581538,"alleles":["C","A"],"strand":1,"feature_type":"variation","id":"rs1798541801","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1467812398","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581542,"source":"dbSNP","strand":1,"feature_type":"variation","end":140581542,"alleles":["C","A","T"]},{"start":140581544,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140581547,"alleles":["TTAG","-"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs759997104","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130633708","clinical_significance":[],"start":140581545,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140581545,"strand":1,"feature_type":"variation"},{"start":140581547,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140581547,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs878864220","clinical_significance":[]},{"start":140581549,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140581549,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798542244","clinical_significance":[]},{"start":140581558,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140581558,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798542346","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798542452","clinical_significance":[],"start":140581560,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140581560,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1798542549","clinical_significance":[],"start":140581565,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140581565,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1049682534","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140581570,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581570,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581571,"feature_type":"variation","strand":1,"end":140581571,"alleles":["G","A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs865932840"},{"id":"rs1270739787","seq_region_name":"7","clinical_significance":[],"end":140581572,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140581572,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581575,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140581575,"clinical_significance":[],"seq_region_name":"7","id":"rs1798543058"},{"alleles":["C","A","G"],"end":140581579,"feature_type":"variation","strand":1,"source":"dbSNP","start":140581579,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798543157"},{"end":140581580,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140581580,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1187257436"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581581,"source":"dbSNP","strand":1,"feature_type":"variation","end":140581581,"alleles":["C","T"],"seq_region_name":"7","id":"rs1798543399","clinical_significance":[]},{"clinical_significance":[],"id":"rs1340856510","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581582,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140581582},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140581583,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581583,"source":"dbSNP","seq_region_name":"7","id":"rs762604762","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1036578722","feature_type":"variation","strand":1,"alleles":["T","A"],"end":140581584,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581584},{"end":140581585,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140581585,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798543830"},{"clinical_significance":[],"id":"rs191565041","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581593,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140581593},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581601,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140581601,"id":"rs901518337","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1346759410","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581609,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140581609},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581611,"source":"dbSNP","strand":1,"feature_type":"variation","end":140581611,"alleles":["G","T"],"seq_region_name":"7","id":"rs1798544266","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1253898346","source":"dbSNP","start":140581613,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140581613,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs947120112","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581619,"source":"dbSNP","strand":1,"feature_type":"variation","end":140581619,"alleles":["G","C"]},{"seq_region_name":"7","id":"rs1798544584","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581621,"source":"dbSNP","strand":1,"feature_type":"variation","end":140581621,"alleles":["C","T"]},{"source":"dbSNP","start":140581622,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140581622,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs978593684"},{"clinical_significance":[],"id":"rs1798544780","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581624,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140581624},{"clinical_significance":[],"id":"rs1299668902","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581626,"feature_type":"variation","strand":1,"end":140581626,"alleles":["G","T"]},{"seq_region_name":"7","id":"rs1798544959","clinical_significance":[],"alleles":["CCCC","CCC"],"end":140581634,"strand":1,"feature_type":"variation","start":140581631,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798545072","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581634,"feature_type":"variation","strand":1,"end":140581634,"alleles":["C","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798545161","feature_type":"variation","strand":1,"end":140581640,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581640},{"seq_region_name":"7","id":"rs1461495891","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140581643,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581643,"source":"dbSNP"},{"clinical_significance":[],"id":"rs556047877","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581645,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140581645},{"seq_region_name":"7","id":"rs997153698","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581646,"source":"dbSNP","strand":1,"feature_type":"variation","end":140581646,"alleles":["A","G"]},{"start":140581648,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140581648,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798545938","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581649,"source":"dbSNP","strand":1,"feature_type":"variation","end":140581649,"alleles":["C","G"],"id":"rs1798546120","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581656,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140581656,"seq_region_name":"7","id":"rs1334651735","clinical_significance":[]},{"end":140581660,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140581660,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798546449","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581664,"source":"dbSNP","strand":1,"feature_type":"variation","end":140581664,"alleles":["T","G"],"id":"rs1798546603","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","A"],"end":140581665,"feature_type":"variation","strand":1,"source":"dbSNP","start":140581665,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1798546781","seq_region_name":"7"},{"source":"dbSNP","start":140581668,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140581668,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1050189725"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798547155","source":"dbSNP","start":140581672,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140581672,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs555692357","source":"dbSNP","start":140581674,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140581674,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1173254264","seq_region_name":"7","alleles":["A","T"],"end":140581675,"feature_type":"variation","strand":1,"source":"dbSNP","start":140581675,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581676,"source":"dbSNP","strand":1,"feature_type":"variation","end":140581676,"alleles":["G","A","T"],"seq_region_name":"7","id":"rs1258731516","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581681,"feature_type":"variation","strand":1,"end":140581681,"alleles":["A","G"],"clinical_significance":[],"id":"rs146357917","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140581685,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581685,"source":"dbSNP","seq_region_name":"7","id":"rs1798547898","clinical_significance":[]},{"alleles":["C","T"],"end":140581688,"feature_type":"variation","strand":1,"source":"dbSNP","start":140581688,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1422491202"},{"end":140581689,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140581689,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1011435321"},{"source":"dbSNP","start":140581690,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140581690,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1187414106"},{"seq_region_name":"7","id":"rs1167232723","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581692,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140581692},{"seq_region_name":"7","id":"rs1449431640","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581693,"source":"dbSNP","strand":1,"feature_type":"variation","end":140581693,"alleles":["A","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581694,"source":"dbSNP","strand":1,"feature_type":"variation","end":140581694,"alleles":["C","A"],"seq_region_name":"7","id":"rs1238404430","clinical_significance":[]},{"source":"dbSNP","start":140581695,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140581695,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1057421712"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581696,"feature_type":"variation","strand":1,"end":140581696,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs917140160"},{"clinical_significance":[],"id":"rs1798549304","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140581697,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581697},{"source":"dbSNP","start":140581700,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140581700,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798549521"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581700,"feature_type":"variation","strand":1,"end":140581715,"alleles":["CCCGCTGAGGGCTTGC","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1209737806"},{"clinical_significance":[],"seq_region_name":"7","id":"rs948746102","alleles":["C","T"],"end":140581702,"feature_type":"variation","strand":1,"source":"dbSNP","start":140581702,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140581703,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581703,"source":"dbSNP","id":"rs9942679","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798550335","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140581706,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581706},{"id":"rs1798550496","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140581714,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581714,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1798550659","seq_region_name":"7","alleles":["A","G"],"end":140581716,"feature_type":"variation","strand":1,"source":"dbSNP","start":140581716,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs751974106","end":140581718,"alleles":["G","C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140581718,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1284722039","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581719,"feature_type":"variation","strand":1,"end":140581719,"alleles":["G","A","T"]},{"clinical_significance":[],"id":"rs1768804472","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140581722,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581722},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140581723,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581723,"source":"dbSNP","id":"rs755520610","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1423098288","feature_type":"variation","strand":1,"end":140581724,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581724},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581728,"feature_type":"variation","strand":1,"end":140581728,"alleles":["C","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1798551672"},{"id":"rs1798551867","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581736,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140581736},{"strand":1,"feature_type":"variation","end":140581738,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581738,"source":"dbSNP","id":"rs999180100","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs527722514","source":"dbSNP","start":140581739,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140581739,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798552476","alleles":["G","A"],"end":140581741,"feature_type":"variation","strand":1,"source":"dbSNP","start":140581741,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798552642","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140581742,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581742},{"source":"dbSNP","start":140581745,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","-"],"end":140581745,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1306328962"},{"start":140581745,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140581745,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798552808","clinical_significance":[]},{"clinical_significance":[],"id":"rs1798553112","seq_region_name":"7","feature_type":"variation","strand":1,"end":140581746,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581746},{"seq_region_name":"7","id":"rs1798553281","clinical_significance":[],"start":140581749,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140581749,"strand":1,"feature_type":"variation"},{"end":140581751,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140581751,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs960713846"},{"feature_type":"variation","strand":1,"end":140581753,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581753,"clinical_significance":[],"id":"rs992103423","seq_region_name":"7"},{"clinical_significance":[],"id":"rs916692620","seq_region_name":"7","end":140581771,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140581771,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["A","G"],"end":140581772,"strand":1,"feature_type":"variation","start":140581772,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1399769486","clinical_significance":[]},{"id":"rs1798554152","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581774,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140581774},{"strand":1,"feature_type":"variation","end":140581775,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581775,"source":"dbSNP","id":"rs1798554314","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs545791086","clinical_significance":[],"alleles":["C","A"],"end":140581776,"strand":1,"feature_type":"variation","start":140581776,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1798554677","clinical_significance":[],"start":140581777,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140581777,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581777,"feature_type":"variation","strand":1,"alleles":["TACAGATACAGATACAG","TACAGATACAG","TACAGATACAGATACAGATACAG"],"end":140581793,"clinical_significance":[],"seq_region_name":"7","id":"rs1165542138"},{"seq_region_name":"7","id":"rs868757289","clinical_significance":[],"alleles":["C","A","G"],"end":140581785,"strand":1,"feature_type":"variation","start":140581785,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs115329359","end":140581789,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140581789,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581790,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140581790,"clinical_significance":[],"id":"rs1212366013","seq_region_name":"7"},{"end":140581792,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140581792,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs753168622","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140581793,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581793,"clinical_significance":[],"seq_region_name":"7","id":"rs1798555688"},{"clinical_significance":[],"seq_region_name":"7","id":"rs756311355","alleles":["C","T"],"end":140581794,"feature_type":"variation","strand":1,"source":"dbSNP","start":140581794,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581796,"source":"dbSNP","strand":1,"feature_type":"variation","end":140581796,"alleles":["G","C"],"seq_region_name":"7","id":"rs1798555915","clinical_significance":[]},{"seq_region_name":"7","id":"rs1328144504","clinical_significance":[],"start":140581799,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G","T"],"end":140581799,"strand":1,"feature_type":"variation"},{"end":140581800,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140581800,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs531897089"},{"source":"dbSNP","start":140581802,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140581818,"alleles":["TAAGTTCTTGTTGACAT","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1798556288","seq_region_name":"7"},{"source":"dbSNP","start":140581812,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140581812,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1277056363"},{"end":140581817,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140581817,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1323747148","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798556604","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581819,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140581819},{"end":140581821,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140581821,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1009034830","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1036630225","clinical_significance":[],"start":140581823,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140581823,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs776960000","feature_type":"variation","strand":1,"end":140581828,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581828},{"end":140581829,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140581829,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798557116","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140581832,"alleles":["GGG","GG"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581830,"source":"dbSNP","seq_region_name":"7","id":"rs1798557272","clinical_significance":[]},{"id":"rs1290450913","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140581831,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581831,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798557597","source":"dbSNP","start":140581832,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140581832,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1229977100","seq_region_name":"7","feature_type":"variation","strand":1,"end":140581833,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581833},{"id":"rs1224946458","seq_region_name":"7","clinical_significance":[],"start":140581836,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140581836,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"end":140581838,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140581838,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs964967140"},{"seq_region_name":"7","id":"rs996940260","clinical_significance":[],"alleles":["G","A","T"],"end":140581840,"strand":1,"feature_type":"variation","start":140581840,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1352621732","end":140581844,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140581844,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1252991670","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140581845,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581845,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1441518993","clinical_significance":[],"end":140581846,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140581846,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1350563345","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581848,"feature_type":"variation","strand":1,"alleles":["GG","G"],"end":140581849},{"clinical_significance":[],"seq_region_name":"7","id":"rs1326084669","feature_type":"variation","strand":1,"end":140581849,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581849},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581853,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140581853,"seq_region_name":"7","id":"rs1027976849","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1482476383","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581859,"feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140581859},{"clinical_significance":[],"seq_region_name":"7","id":"rs923492495","end":140581861,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140581861,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140581865,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581865,"clinical_significance":[],"seq_region_name":"7","id":"rs778018907"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581869,"feature_type":"variation","strand":1,"end":140581869,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1798559736"},{"clinical_significance":[],"seq_region_name":"7","id":"rs550365685","feature_type":"variation","strand":1,"end":140581874,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581874},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130634630","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581878,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140581878},{"start":140581879,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140581883,"alleles":["AGTGA","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1473782608","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140581882,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581882,"clinical_significance":[],"id":"rs1585683972","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1413626410","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581885,"feature_type":"variation","strand":1,"end":140581885,"alleles":["A","G"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581885,"feature_type":"variation","strand":1,"alleles":["AAGAAGAA","AAGAA"],"end":140581892,"clinical_significance":[],"id":"rs1262967851","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1050073506","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581886,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140581886},{"feature_type":"variation","strand":1,"end":140581887,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581887,"clinical_significance":[],"seq_region_name":"7","id":"rs1655059097"},{"id":"rs1175147038","seq_region_name":"7","clinical_significance":[],"end":140581888,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140581888,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs968474919","clinical_significance":[],"start":140581891,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140581894,"alleles":["AAAA","AAAAA"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1798560995","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581892,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140581892},{"end":140581893,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140581893,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585684030","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581896,"feature_type":"variation","strand":1,"end":140581896,"alleles":["G","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs183338420"},{"source":"dbSNP","start":140581897,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140581897,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1191545376","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140581898,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581898,"source":"dbSNP","id":"rs978480418","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140581900,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581900,"clinical_significance":[],"seq_region_name":"7","id":"rs749334604"},{"clinical_significance":[],"id":"rs1480832459","seq_region_name":"7","end":140581901,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140581901,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140581906,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581906,"clinical_significance":[],"seq_region_name":"7","id":"rs1178501764"},{"end":140581910,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140581910,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs955882202","clinical_significance":[]},{"alleles":["T","C"],"end":140581917,"feature_type":"variation","strand":1,"source":"dbSNP","start":140581917,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1286633551"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798562074","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581919,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140581919},{"id":"rs1798562216","seq_region_name":"7","clinical_significance":[],"start":140581922,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140581922,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140581923,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581923,"source":"dbSNP","seq_region_name":"7","id":"rs1798562320","clinical_significance":[]},{"id":"rs1798562422","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140581926,"strand":1,"feature_type":"variation","start":140581926,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1223481351","clinical_significance":[],"start":140581927,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140581927,"alleles":["G","A","C"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581929,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140581929,"seq_region_name":"7","id":"rs1798562640","clinical_significance":[]},{"alleles":["G","T"],"end":140581930,"strand":1,"feature_type":"variation","start":140581930,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1798562743","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs371060487","feature_type":"variation","strand":1,"end":140581932,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581932},{"seq_region_name":"7","id":"rs542404721","clinical_significance":[],"end":140581933,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140581933,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581934,"feature_type":"variation","strand":1,"end":140581934,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1434931341"},{"seq_region_name":"7","id":"rs1798563168","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581935,"source":"dbSNP","strand":1,"feature_type":"variation","end":140581935,"alleles":["T","C"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581936,"source":"dbSNP","strand":1,"feature_type":"variation","end":140581936,"alleles":["T","C"],"seq_region_name":"7","id":"rs1798563298","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140581940,"alleles":["CTGC","CTGCTGC"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581937,"source":"dbSNP","id":"rs1370836079","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1798563523","seq_region_name":"7","end":140581939,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140581939,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","T"],"end":140581941,"feature_type":"variation","strand":1,"source":"dbSNP","start":140581941,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1798563616","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140581954,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581954,"clinical_significance":[],"seq_region_name":"7","id":"rs1798563735"},{"clinical_significance":[],"seq_region_name":"7","id":"rs947122491","source":"dbSNP","start":140581958,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140581958,"alleles":["C","G"],"feature_type":"variation","strand":1},{"start":140581962,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140581962,"alleles":["G","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1459115735","clinical_significance":[]},{"start":140581968,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140581967,"alleles":["-","CG"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs765316646","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581968,"feature_type":"variation","strand":1,"end":140581968,"alleles":["T","TT","TTT"],"clinical_significance":[],"seq_region_name":"7","id":"rs372515936"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1554473256","end":140581970,"alleles":["TGT","TGTGT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140581968,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581968,"feature_type":"variation","strand":1,"alleles":["TGTT","T"],"end":140581971,"clinical_significance":[],"seq_region_name":"7","id":"rs1563156724"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581969,"source":"dbSNP","strand":1,"feature_type":"variation","end":140581969,"alleles":["G","A","T"],"seq_region_name":"7","id":"rs2018505","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","-"],"end":140581969,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581969,"clinical_significance":[],"seq_region_name":"7","id":"rs202134537"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581970,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140581970,"clinical_significance":[],"id":"rs1798564540","seq_region_name":"7"},{"source":"dbSNP","start":140581970,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140581970,"alleles":["T","TGTT"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798564646"},{"start":140581970,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TTTTTTTTTTTTT","TTTTTTTTTTT","TTTTTTTTTTTT","TTTTTTTTTTTTTT","TTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTT"],"end":140581982,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs373264245","clinical_significance":[]},{"seq_region_name":"7","id":"rs11418260","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581971,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["-","G"],"end":140581970},{"seq_region_name":"7","id":"rs1281015337","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581971,"source":"dbSNP","strand":1,"feature_type":"variation","end":140581971,"alleles":["T","G"]},{"seq_region_name":"7","id":"rs2130634985","clinical_significance":[],"alleles":["T","G"],"end":140581972,"strand":1,"feature_type":"variation","start":140581972,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["T","C"],"end":140581975,"feature_type":"variation","strand":1,"source":"dbSNP","start":140581975,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs548344409"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798565434","alleles":["-","G"],"end":140581975,"feature_type":"variation","strand":1,"source":"dbSNP","start":140581976,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140581978,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["-","C"],"end":140581977,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1217477920","clinical_significance":[]},{"seq_region_name":"7","id":"rs868220113","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581983,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C","T"],"end":140581983},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581983,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GAGACAGAGTTTCACTC","-"],"end":140581999,"seq_region_name":"7","id":"rs1798565819","clinical_significance":[]},{"clinical_significance":[],"id":"rs1437958616","seq_region_name":"7","alleles":["AGAG","AG"],"end":140581991,"feature_type":"variation","strand":1,"source":"dbSNP","start":140581988,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1798566057","clinical_significance":[],"start":140581989,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140581989,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140581997,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140581997,"clinical_significance":[],"seq_region_name":"7","id":"rs1288722704"},{"seq_region_name":"7","id":"rs372251841","clinical_significance":[],"start":140581997,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140582000,"alleles":["CTCT","CT"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140581998,"source":"dbSNP","strand":1,"feature_type":"variation","end":140581998,"alleles":["T","A","G"],"seq_region_name":"7","id":"rs1798566415","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582000,"source":"dbSNP","strand":1,"feature_type":"variation","end":140582003,"alleles":["TTTT","TT"],"seq_region_name":"7","id":"rs1798566550","clinical_significance":[]},{"end":140582001,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140582001,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1429574035","seq_region_name":"7"},{"source":"dbSNP","start":140582006,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140582006,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1359317152","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1798566876","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582008,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140582008},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582017,"source":"dbSNP","strand":1,"feature_type":"variation","end":140582017,"alleles":["T","C","G"],"seq_region_name":"7","id":"rs1177833869","clinical_significance":[]},{"start":140582022,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140582022,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1432272569","clinical_significance":[]},{"clinical_significance":[],"id":"rs1394005922","seq_region_name":"7","alleles":["T","A"],"end":140582030,"feature_type":"variation","strand":1,"source":"dbSNP","start":140582030,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1169109189","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582032,"source":"dbSNP","strand":1,"feature_type":"variation","end":140582032,"alleles":["T","C"]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140582033,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582033,"source":"dbSNP","seq_region_name":"7","id":"rs1798567430","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140582038,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582038,"clinical_significance":[],"seq_region_name":"7","id":"rs1798567537"},{"seq_region_name":"7","id":"rs566568433","clinical_significance":[],"strand":1,"feature_type":"variation","end":140582041,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582041,"source":"dbSNP"},{"start":140582042,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140582042,"strand":1,"feature_type":"variation","id":"rs533799558","seq_region_name":"7","clinical_significance":[]},{"start":140582046,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140582046,"strand":1,"feature_type":"variation","id":"rs1298728068","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582047,"feature_type":"variation","strand":1,"end":140582047,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1798567952"},{"clinical_significance":[],"id":"rs1798568046","seq_region_name":"7","source":"dbSNP","start":140582052,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140582052,"feature_type":"variation","strand":1},{"alleles":["CCCCCC","CCCCC"],"end":140582057,"strand":1,"feature_type":"variation","start":140582052,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1798568153","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","T"],"end":140582053,"strand":1,"feature_type":"variation","start":140582053,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1185661336","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130635167","clinical_significance":[],"start":140582055,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140582055,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582057,"feature_type":"variation","strand":1,"end":140582057,"alleles":["C","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs551870437"},{"seq_region_name":"7","id":"rs920589968","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582059,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140582059},{"alleles":["G","T"],"end":140582060,"feature_type":"variation","strand":1,"source":"dbSNP","start":140582060,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798568589"},{"end":140582065,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140582065,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1239389665","seq_region_name":"7","clinical_significance":[]},{"end":140582074,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140582074,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1035595780","clinical_significance":[]},{"seq_region_name":"7","id":"rs757285856","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140582080,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582080,"source":"dbSNP"},{"start":140582082,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140582082,"alleles":["T","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1275488452","clinical_significance":[]},{"start":140582083,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140582083,"alleles":["G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798569138","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140582084,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582084,"source":"dbSNP","seq_region_name":"7","id":"rs1311267450","clinical_significance":[]},{"seq_region_name":"7","id":"rs1295516287","clinical_significance":[],"alleles":["C","T"],"end":140582087,"strand":1,"feature_type":"variation","start":140582087,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582089,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140582089,"clinical_significance":[],"id":"rs895724396","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140582090,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582090,"source":"dbSNP","id":"rs531034213","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1356410311","end":140582092,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140582092,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1215059010","clinical_significance":[],"start":140582096,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140582096,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1304202061","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582097,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140582097},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798570042","alleles":["A","T"],"end":140582101,"feature_type":"variation","strand":1,"source":"dbSNP","start":140582101,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1563156833","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582102,"feature_type":"variation","strand":1,"end":140582102,"alleles":["T","A","C"]},{"id":"rs2130635313","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140582105,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582105,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1412586952","seq_region_name":"7","feature_type":"variation","strand":1,"end":140582106,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582106},{"seq_region_name":"7","id":"rs1585684539","clinical_significance":[],"end":140582110,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","start":140582110,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs570737798","alleles":["C","A","T"],"end":140582113,"feature_type":"variation","strand":1,"source":"dbSNP","start":140582113,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs967194061","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582114,"feature_type":"variation","strand":1,"end":140582114,"alleles":["G","A","C"]},{"id":"rs1798570791","seq_region_name":"7","clinical_significance":[],"start":140582115,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140582115,"strand":1,"feature_type":"variation"},{"alleles":["C","T"],"end":140582118,"strand":1,"feature_type":"variation","start":140582118,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130635354","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798570888","source":"dbSNP","start":140582120,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140582120,"alleles":["A","C","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1431122060","seq_region_name":"7","end":140582121,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140582121,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["CACC","-"],"end":140582124,"feature_type":"variation","strand":1,"source":"dbSNP","start":140582121,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130635375"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798571138","source":"dbSNP","start":140582123,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140582123,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798571270","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582126,"feature_type":"variation","strand":1,"end":140582126,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs2130635401","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582127,"source":"dbSNP","strand":1,"feature_type":"variation","end":140582126,"alleles":["-","CCCA"]},{"seq_region_name":"7","id":"rs1371204583","clinical_significance":[],"strand":1,"feature_type":"variation","end":140582131,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582131,"source":"dbSNP"},{"start":140582140,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140582140,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs969379187","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798571573","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582141,"feature_type":"variation","strand":1,"end":140582141,"alleles":["T","A"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582144,"source":"dbSNP","strand":1,"feature_type":"variation","end":140582144,"alleles":["T","C"],"id":"rs1424123288","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582146,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140582146,"seq_region_name":"7","id":"rs1193005027","clinical_significance":[]},{"end":140582147,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140582147,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs985289752","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582149,"source":"dbSNP","strand":1,"feature_type":"variation","end":140582149,"alleles":["G","C"],"seq_region_name":"7","id":"rs1798571983","clinical_significance":[]},{"start":140582151,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140582151,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1265449865","clinical_significance":[]},{"clinical_significance":[],"id":"rs374445999","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582153,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140582153},{"strand":1,"feature_type":"variation","end":140582157,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582157,"source":"dbSNP","seq_region_name":"7","id":"rs1798572314","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1432850511","alleles":["C","T"],"end":140582161,"feature_type":"variation","strand":1,"source":"dbSNP","start":140582161,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582162,"feature_type":"variation","strand":1,"end":140582162,"alleles":["A","C","G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs87156"},{"end":140582163,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140582163,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1381909703"},{"clinical_significance":[],"seq_region_name":"7","id":"rs962539506","end":140582166,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140582166,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140582171,"alleles":["TGTTGG","TGTTGGTGTTGG"],"strand":1,"feature_type":"variation","start":140582166,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798573147","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1479700408","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582171,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140582171},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582172,"source":"dbSNP","strand":1,"feature_type":"variation","end":140582172,"alleles":["C","T"],"seq_region_name":"7","id":"rs1251197932","clinical_significance":[]},{"seq_region_name":"7","id":"rs1223011081","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140582176,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582176,"source":"dbSNP"},{"id":"rs1323847609","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582178,"source":"dbSNP","strand":1,"feature_type":"variation","end":140582178,"alleles":["T","G"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582180,"source":"dbSNP","strand":1,"feature_type":"variation","end":140582180,"alleles":["G","A"],"id":"rs1798573701","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798573829","clinical_significance":[],"start":140582182,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140582182,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798573925","end":140582183,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140582183,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1798574039","seq_region_name":"7","source":"dbSNP","start":140582187,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140582187,"alleles":["A","C"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582195,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140582195,"clinical_significance":[],"seq_region_name":"7","id":"rs1417671906"},{"seq_region_name":"7","id":"rs1798574256","clinical_significance":[],"end":140582196,"alleles":["CC","CCC"],"strand":1,"feature_type":"variation","start":140582195,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140582198,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140582198,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1291896680","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798574459","feature_type":"variation","strand":1,"end":140582199,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582199},{"end":140582200,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140582200,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585684735"},{"seq_region_name":"7","id":"rs1585684745","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582201,"source":"dbSNP","strand":1,"feature_type":"variation","end":140582201,"alleles":["G","C"]},{"clinical_significance":[],"id":"rs1585684754","seq_region_name":"7","end":140582202,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140582202,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140582203,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582203,"clinical_significance":[],"seq_region_name":"7","id":"rs1798575017"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798575187","end":140582204,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140582204,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140582207,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140582207,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1798575282","seq_region_name":"7"},{"seq_region_name":"7","id":"rs972206165","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582208,"source":"dbSNP","strand":1,"feature_type":"variation","end":140582208,"alleles":["A","C","G"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582211,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140582211,"seq_region_name":"7","id":"rs113638623","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140582212,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582212,"source":"dbSNP","id":"rs1366184027","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140582218,"alleles":["GG","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582217,"source":"dbSNP","seq_region_name":"7","id":"rs1798575777","clinical_significance":[]},{"clinical_significance":[],"id":"rs1458945856","seq_region_name":"7","end":140582220,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140582220,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","G"],"end":140582222,"strand":1,"feature_type":"variation","start":140582222,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798575987","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1288595886","feature_type":"variation","strand":1,"end":140582223,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582223},{"clinical_significance":[],"seq_region_name":"7","id":"rs1411089099","source":"dbSNP","start":140582227,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140582227,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs933548850","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582232,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140582232},{"seq_region_name":"7","id":"rs1798576457","clinical_significance":[],"start":140582238,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140582238,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"end":140582240,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140582240,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1291295756","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798576710","source":"dbSNP","start":140582241,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140582241,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140582244,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582244,"clinical_significance":[],"seq_region_name":"7","id":"rs1798576815"},{"clinical_significance":[],"id":"rs1798576931","seq_region_name":"7","alleles":["G","T"],"end":140582247,"feature_type":"variation","strand":1,"source":"dbSNP","start":140582247,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140582248,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582248,"clinical_significance":[],"seq_region_name":"7","id":"rs764590550"},{"end":140582254,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140582254,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs910212257"},{"alleles":["G","A"],"end":140582255,"feature_type":"variation","strand":1,"source":"dbSNP","start":140582255,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798577337"},{"clinical_significance":[],"seq_region_name":"7","id":"rs370295275","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582256,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140582256},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140582257,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582257,"source":"dbSNP","seq_region_name":"7","id":"rs1162597771","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582259,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140582259,"id":"rs1798577690","seq_region_name":"7","clinical_significance":[]},{"end":140582263,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140582263,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs370486049","clinical_significance":[]},{"source":"dbSNP","start":140582267,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140582267,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs968358400","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1798578019","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140582269,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582269},{"end":140582271,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140582271,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1718019597"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140582272,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582272,"clinical_significance":[],"seq_region_name":"7","id":"rs574250951"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582274,"feature_type":"variation","strand":1,"end":140582274,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs902915134"},{"alleles":["T","C"],"end":140582276,"feature_type":"variation","strand":1,"source":"dbSNP","start":140582276,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1285860454"},{"start":140582278,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140582278,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs1249960495","seq_region_name":"7","clinical_significance":[]},{"start":140582279,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140582279,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798578544","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798578651","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582281,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140582281},{"seq_region_name":"7","id":"rs1798578737","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140582284,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582284,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140582287,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582287,"source":"dbSNP","seq_region_name":"7","id":"rs1798578837","clinical_significance":[]},{"seq_region_name":"7","id":"rs1192277875","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582291,"source":"dbSNP","strand":1,"feature_type":"variation","end":140582291,"alleles":["A","-"]},{"alleles":["G","A"],"end":140582293,"feature_type":"variation","strand":1,"source":"dbSNP","start":140582293,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798579072"},{"id":"rs1489788403","seq_region_name":"7","clinical_significance":[],"end":140582295,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140582295,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1360797683","feature_type":"variation","strand":1,"end":140582296,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582296},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582297,"source":"dbSNP","strand":1,"feature_type":"variation","end":140582297,"alleles":["G","A"],"id":"rs1271845587","seq_region_name":"7","clinical_significance":[]},{"end":140582300,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140582300,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798579514"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585684978","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582302,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140582302},{"seq_region_name":"7","id":"rs934525290","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582306,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140582306},{"alleles":["C","T"],"end":140582308,"feature_type":"variation","strand":1,"source":"dbSNP","start":140582308,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798579859"},{"id":"rs1798579976","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582309,"source":"dbSNP","strand":1,"feature_type":"variation","end":140582309,"alleles":["T","A"]},{"seq_region_name":"7","id":"rs1798580072","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140582310,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582310,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798580208","source":"dbSNP","start":140582310,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140582313,"alleles":["CCCC","CCC"],"feature_type":"variation","strand":1},{"start":140582311,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140582311,"alleles":["C","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798580323","clinical_significance":[]},{"clinical_significance":[],"id":"rs56239414","seq_region_name":"7","end":140582313,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140582313,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582314,"feature_type":"variation","strand":1,"end":140582314,"alleles":["G","A","C","T"],"clinical_significance":[],"id":"rs895776826","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1012791867","alleles":["C","T"],"end":140582315,"feature_type":"variation","strand":1,"source":"dbSNP","start":140582315,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1263779562","feature_type":"variation","strand":1,"end":140582323,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582323},{"id":"rs1585685040","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140582326,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582326,"source":"dbSNP"},{"alleles":["C","T"],"end":140582329,"feature_type":"variation","strand":1,"source":"dbSNP","start":140582329,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1268314814","seq_region_name":"7"},{"start":140582329,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["CCAGGTAGGACCCAG","CCAG"],"end":140582343,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1488223973","clinical_significance":[]},{"source":"dbSNP","start":140582330,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140582330,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130636017"},{"id":"rs1798581269","seq_region_name":"7","clinical_significance":[],"start":140582331,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140582331,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1022805776","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140582332,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582332,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140582344,"alleles":["A","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582344,"clinical_significance":[],"seq_region_name":"7","id":"rs1798581479"},{"seq_region_name":"7","id":"rs1798581596","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582345,"source":"dbSNP","strand":1,"feature_type":"variation","end":140582345,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs553897729","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140582348,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582348},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798581826","source":"dbSNP","start":140582350,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140582350,"feature_type":"variation","strand":1},{"start":140582354,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140582354,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798581938","clinical_significance":[]},{"clinical_significance":[],"id":"rs1177963284","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582355,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140582355},{"seq_region_name":"7","id":"rs905206743","clinical_significance":[],"strand":1,"feature_type":"variation","end":140582358,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582358,"source":"dbSNP"},{"end":140582360,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140582360,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1240329837","clinical_significance":[]},{"start":140582366,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140582366,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs746865114","clinical_significance":[]},{"source":"dbSNP","start":140582370,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140582370,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130636114"},{"seq_region_name":"7","id":"rs955769585","clinical_significance":[],"start":140582373,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140582382,"alleles":["TTCTTCTTCT","TTCTTCT"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130636127","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140582377,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582377},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140582387,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582387,"clinical_significance":[],"seq_region_name":"7","id":"rs1798582648"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798582758","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582390,"feature_type":"variation","strand":1,"end":140582390,"alleles":["G","C"]},{"id":"rs1169327908","seq_region_name":"7","clinical_significance":[],"start":140582399,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140582399,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"id":"rs572187777","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140582402,"strand":1,"feature_type":"variation","start":140582402,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1798583076","seq_region_name":"7","source":"dbSNP","start":140582403,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140582403,"alleles":["G","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1016783099","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582411,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140582411},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140582413,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582413,"clinical_significance":[],"seq_region_name":"7","id":"rs764033624"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798583402","source":"dbSNP","start":140582422,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140582422,"alleles":["A","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798583504","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582423,"feature_type":"variation","strand":1,"end":140582423,"alleles":["A","G"]},{"clinical_significance":[],"id":"rs1798583604","seq_region_name":"7","end":140582424,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140582424,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["T","C"],"end":140582425,"feature_type":"variation","strand":1,"source":"dbSNP","start":140582425,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798583724"},{"strand":1,"feature_type":"variation","end":140582427,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582427,"source":"dbSNP","id":"rs190572286","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1323810413","clinical_significance":[],"alleles":["T","C"],"end":140582436,"strand":1,"feature_type":"variation","start":140582436,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140582437,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140582437,"alleles":["C","G"],"strand":1,"feature_type":"variation","id":"rs1177791859","seq_region_name":"7","clinical_significance":[]},{"id":"rs917079184","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140582438,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582438,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1798584314","seq_region_name":"7","alleles":["C","T"],"end":140582439,"feature_type":"variation","strand":1,"source":"dbSNP","start":140582439,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582440,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140582440,"seq_region_name":"7","id":"rs1585685227","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798584520","source":"dbSNP","start":140582442,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140582442,"feature_type":"variation","strand":1},{"alleles":["T","C"],"end":140582443,"strand":1,"feature_type":"variation","start":140582443,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs2130636265","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585685238","source":"dbSNP","start":140582444,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140582444,"feature_type":"variation","strand":1},{"alleles":["C","T"],"end":140582445,"feature_type":"variation","strand":1,"source":"dbSNP","start":140582445,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130636284"},{"seq_region_name":"7","id":"rs751426118","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582447,"source":"dbSNP","strand":1,"feature_type":"variation","end":140582447,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs980044904","source":"dbSNP","start":140582454,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140582454,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs920474378","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582455,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140582455},{"end":140582455,"alleles":["-","T"],"strand":1,"feature_type":"variation","start":140582456,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1162038238","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1030499687","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582456,"feature_type":"variation","strand":1,"alleles":["C","A","G","T"],"end":140582456},{"end":140582457,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140582457,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1199604103"},{"start":140582461,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140582461,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs954819665","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1462087799","alleles":["ACACATTTCCAAGGCAAG","-"],"end":140582479,"feature_type":"variation","strand":1,"source":"dbSNP","start":140582462,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140582464,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582464,"clinical_significance":[],"id":"rs1251637685","seq_region_name":"7"},{"start":140582469,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140582469,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798585887","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798586002","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140582477,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582477,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140582480,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582480,"clinical_significance":[],"seq_region_name":"7","id":"rs1798586114"},{"seq_region_name":"7","id":"rs986388361","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140582481,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582481,"source":"dbSNP"},{"id":"rs1465609911","seq_region_name":"7","clinical_significance":[],"start":140582484,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140582484,"alleles":["G","A","C"],"strand":1,"feature_type":"variation"},{"alleles":["A","G"],"end":140582485,"feature_type":"variation","strand":1,"source":"dbSNP","start":140582485,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798586485"},{"clinical_significance":[],"id":"rs1798586594","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582493,"feature_type":"variation","strand":1,"end":140582493,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798586722","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582509,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140582509},{"alleles":["T","C"],"end":140582510,"strand":1,"feature_type":"variation","start":140582510,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs146627078","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140582512,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582512,"source":"dbSNP","id":"rs947065477","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1206518587","feature_type":"variation","strand":1,"end":140582527,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582527},{"seq_region_name":"7","id":"rs1348167982","clinical_significance":[],"start":140582528,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140582528,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1444941336","alleles":["C","A","T"],"end":140582529,"feature_type":"variation","strand":1,"source":"dbSNP","start":140582529,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582531,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140582531,"seq_region_name":"7","id":"rs761475880","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582539,"feature_type":"variation","strand":1,"end":140582539,"alleles":["T","C"],"clinical_significance":[],"id":"rs1798587577","seq_region_name":"7"},{"source":"dbSNP","start":140582542,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140582542,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1384116403"},{"id":"rs907982734","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140582543,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582543,"source":"dbSNP"},{"start":140582544,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140582544,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1349459207","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140582545,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582545,"clinical_significance":[],"id":"rs1798588056","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582549,"feature_type":"variation","strand":1,"end":140582549,"alleles":["G","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1798588172"},{"source":"dbSNP","start":140582550,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140582550,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798588277"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798588378","alleles":["C","G","T"],"end":140582563,"feature_type":"variation","strand":1,"source":"dbSNP","start":140582563,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1585685450","seq_region_name":"7","source":"dbSNP","start":140582564,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140582564,"alleles":["T","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1301096123","clinical_significance":[],"start":140582568,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140582568,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1798588765","clinical_significance":[],"end":140582573,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140582573,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140582574,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140582574,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798588882","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582576,"feature_type":"variation","strand":1,"end":140582576,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585685465"},{"id":"rs1798589103","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582577,"source":"dbSNP","strand":1,"feature_type":"variation","end":140582577,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1798589212","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582579,"source":"dbSNP","strand":1,"feature_type":"variation","end":140582579,"alleles":["T","C"]},{"alleles":["T","A","C"],"end":140582582,"strand":1,"feature_type":"variation","start":140582582,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1311256249","clinical_significance":[]},{"source":"dbSNP","start":140582588,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140582588,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798589489"},{"seq_region_name":"7","id":"rs1365659471","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582591,"source":"dbSNP","strand":1,"feature_type":"variation","end":140582591,"alleles":["A","T"]},{"seq_region_name":"7","id":"rs1321190189","clinical_significance":[],"alleles":["C","A"],"end":140582593,"strand":1,"feature_type":"variation","start":140582593,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140582595,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140582595,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs62485840","seq_region_name":"7"},{"id":"rs1798589934","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140582596,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582596,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1320112229","clinical_significance":[],"start":140582600,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140582600,"alleles":["T","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798590139","end":140582601,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140582601,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140582604,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582604,"clinical_significance":[],"seq_region_name":"7","id":"rs978438532"},{"id":"rs1380327657","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582606,"source":"dbSNP","strand":1,"feature_type":"variation","end":140582606,"alleles":["A","T"]},{"start":140582610,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140582610,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1384448688","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs924390732","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582613,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140582613},{"alleles":["T","C","G"],"end":140582621,"feature_type":"variation","strand":1,"source":"dbSNP","start":140582621,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs113003359"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582622,"feature_type":"variation","strand":1,"end":140582622,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs944796132"},{"feature_type":"variation","strand":1,"end":140582630,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582630,"clinical_significance":[],"seq_region_name":"7","id":"rs1798590989"},{"seq_region_name":"7","id":"rs1040978632","clinical_significance":[],"end":140582632,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140582632,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["T","C"],"end":140582633,"strand":1,"feature_type":"variation","start":140582633,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1205378535","seq_region_name":"7","clinical_significance":[]},{"start":140582636,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140582636,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798591373","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798591467","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140582647,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582647},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798591575","alleles":["C","T"],"end":140582649,"feature_type":"variation","strand":1,"source":"dbSNP","start":140582649,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798591676","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582661,"feature_type":"variation","strand":1,"end":140582661,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1173526261","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140582662,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582662,"source":"dbSNP"},{"alleles":["T","C"],"end":140582666,"strand":1,"feature_type":"variation","start":140582666,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798591892","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582667,"source":"dbSNP","strand":1,"feature_type":"variation","end":140582667,"alleles":["C","T"],"seq_region_name":"7","id":"rs1798592005","clinical_significance":[]},{"id":"rs934409147","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140582668,"strand":1,"feature_type":"variation","start":140582668,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140582669,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140582669,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798592198","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1450706551","source":"dbSNP","start":140582676,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140582676,"feature_type":"variation","strand":1},{"end":140582684,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140582684,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585685624","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798592507","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582690,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140582690},{"seq_region_name":"7","id":"rs1260178007","clinical_significance":[],"start":140582692,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140582692,"alleles":["G","A","C"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140582695,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140582695,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1392396357"},{"id":"rs1191411446","seq_region_name":"7","clinical_significance":[],"end":140582698,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140582698,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130636794","end":140582704,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140582704,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["T","G"],"end":140582705,"strand":1,"feature_type":"variation","start":140582705,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1585685651","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582716,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140582716,"clinical_significance":[],"seq_region_name":"7","id":"rs1456617322"},{"clinical_significance":[],"seq_region_name":"7","id":"rs139988525","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140582717,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582717},{"id":"rs1585685667","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140582718,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582718,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140582719,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582719,"source":"dbSNP","seq_region_name":"7","id":"rs1798593381","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585685674","source":"dbSNP","start":140582721,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140582721,"feature_type":"variation","strand":1},{"alleles":["G","A"],"end":140582722,"feature_type":"variation","strand":1,"source":"dbSNP","start":140582722,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs932104487"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582723,"feature_type":"variation","strand":1,"end":140582723,"alleles":["C","T"],"clinical_significance":[],"id":"rs1243555214","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582724,"source":"dbSNP","strand":1,"feature_type":"variation","end":140582724,"alleles":["C","T"],"seq_region_name":"7","id":"rs1798593858","clinical_significance":[]},{"start":140582726,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140582726,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130636869","clinical_significance":[]},{"alleles":["C","T"],"end":140582727,"strand":1,"feature_type":"variation","start":140582727,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs917089886","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1180015923","source":"dbSNP","start":140582728,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140582728,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798594200","end":140582731,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140582731,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140582733,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140582733,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798594303"},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140582736,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582736,"clinical_significance":[],"seq_region_name":"7","id":"rs1798594406"},{"feature_type":"variation","strand":1,"end":140582737,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582737,"clinical_significance":[],"seq_region_name":"7","id":"rs1798594510"},{"clinical_significance":[],"seq_region_name":"7","id":"rs563693167","feature_type":"variation","strand":1,"end":140582739,"alleles":["T","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582739},{"id":"rs904086059","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140582745,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582745,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582747,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140582747,"seq_region_name":"7","id":"rs999838710","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798594890","clinical_significance":[],"alleles":["G","A"],"end":140582748,"strand":1,"feature_type":"variation","start":140582748,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs948529805","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140582750,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582750,"source":"dbSNP"},{"id":"rs1798595140","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140582752,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582752,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140582759,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582759,"source":"dbSNP","seq_region_name":"7","id":"rs2130636956","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582770,"feature_type":"variation","strand":1,"end":140582770,"alleles":["T","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1798595317"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140582773,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582773,"source":"dbSNP","seq_region_name":"7","id":"rs1031281038","clinical_significance":[]},{"start":140582774,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140582774,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1224922091","clinical_significance":[]},{"source":"dbSNP","start":140582775,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140582775,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798595888"},{"id":"rs1428532123","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582777,"source":"dbSNP","strand":1,"feature_type":"variation","end":140582777,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1172196069","clinical_significance":[],"strand":1,"feature_type":"variation","end":140582786,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582786,"source":"dbSNP"},{"alleles":["G","T"],"end":140582788,"feature_type":"variation","strand":1,"source":"dbSNP","start":140582788,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798596435"},{"id":"rs1798596606","seq_region_name":"7","clinical_significance":[],"start":140582794,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140582794,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs776286786","clinical_significance":[],"start":140582797,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140582797,"alleles":["T","G"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140582798,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140582798,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1420970514"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582800,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140582800,"seq_region_name":"7","id":"rs1044725855","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798597107","clinical_significance":[],"alleles":["A","G"],"end":140582801,"strand":1,"feature_type":"variation","start":140582801,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140582802,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582802,"clinical_significance":[],"id":"rs149867166","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs748014201","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582806,"feature_type":"variation","strand":1,"end":140582806,"alleles":["A","C"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582807,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140582807,"clinical_significance":[],"seq_region_name":"7","id":"rs769551847"},{"seq_region_name":"7","id":"rs1798597608","clinical_significance":[],"start":140582813,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140582813,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1430497391","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582821,"source":"dbSNP","strand":1,"feature_type":"variation","end":140582821,"alleles":["C","T"]},{"source":"dbSNP","start":140582823,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140582823,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798597953"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1422186678","feature_type":"variation","strand":1,"end":140582827,"alleles":["GGTAC","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582823},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582824,"feature_type":"variation","strand":1,"end":140582824,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1037698413"},{"alleles":["C","T"],"end":140582827,"strand":1,"feature_type":"variation","start":140582827,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798598665","clinical_significance":[]},{"id":"rs2130637108","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140582828,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582828,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1166694733","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582833,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140582833},{"source":"dbSNP","start":140582834,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TT","T"],"end":140582835,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798598976"},{"start":140582836,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140582836,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1024434123","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140582839,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582839,"clinical_significance":[],"seq_region_name":"7","id":"rs1798599350"},{"id":"rs767495368","seq_region_name":"7","clinical_significance":[],"alleles":["T","C","G"],"end":140582846,"strand":1,"feature_type":"variation","start":140582846,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582850,"source":"dbSNP","strand":1,"feature_type":"variation","end":140582850,"alleles":["A","G"],"seq_region_name":"7","id":"rs183102214","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582851,"feature_type":"variation","strand":1,"end":140582851,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs897942183"},{"start":140582854,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140582854,"alleles":["A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130637172","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582857,"source":"dbSNP","strand":1,"feature_type":"variation","end":140582857,"alleles":["A","G"],"seq_region_name":"7","id":"rs1187813054","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1476017843","source":"dbSNP","start":140582858,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140582858,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140582863,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582863,"source":"dbSNP","seq_region_name":"7","id":"rs1798600395","clinical_significance":[]},{"end":140582869,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140582869,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1360076067","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798600739","clinical_significance":[],"strand":1,"feature_type":"variation","end":140582881,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582881,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1254977300","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140582883,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582883,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1798601047","clinical_significance":[],"alleles":["C","T"],"end":140582888,"strand":1,"feature_type":"variation","start":140582888,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs993584382","clinical_significance":[],"strand":1,"feature_type":"variation","end":140582889,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582889,"source":"dbSNP"},{"start":140582895,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140582895,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1030386685","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582898,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140582898,"clinical_significance":[],"seq_region_name":"7","id":"rs1483117372"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582899,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140582899,"seq_region_name":"7","id":"rs1301588480","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798601865","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140582903,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582903},{"seq_region_name":"7","id":"rs1798601990","clinical_significance":[],"strand":1,"feature_type":"variation","end":140582905,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582905,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140582908,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582908,"source":"dbSNP","seq_region_name":"7","id":"rs1798602094","clinical_significance":[]},{"seq_region_name":"7","id":"rs565989475","clinical_significance":[],"start":140582911,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140582929,"alleles":["TTTCTTTCTTTCTTTCTTT","TTTCTTTCTTTCTTT","TTTCTTTCTTTCTTTCTTTCTTT"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140582915,"alleles":["TCT","TCTATCT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582913,"clinical_significance":[],"seq_region_name":"7","id":"rs1194058043"},{"feature_type":"variation","strand":1,"end":140582917,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582917,"clinical_significance":[],"id":"rs1798602520","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582938,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140582938,"seq_region_name":"7","id":"rs954871048","clinical_significance":[]},{"source":"dbSNP","start":140582942,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140582942,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1798602745","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1338473338","clinical_significance":[],"end":140582943,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140582943,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1284631985","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140582944,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582944,"source":"dbSNP"},{"seq_region_name":"7","id":"rs269235","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140582950,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582950,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1798603208","clinical_significance":[],"strand":1,"feature_type":"variation","end":140582952,"alleles":["C","A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582952,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140582953,"alleles":["CC","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582952,"source":"dbSNP","id":"rs1798603332","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1018303972","clinical_significance":[],"start":140582953,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140582953,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"start":140582955,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140582955,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798603543","clinical_significance":[]},{"id":"rs1798603650","seq_region_name":"7","clinical_significance":[],"end":140582957,"alleles":["T","C","G"],"strand":1,"feature_type":"variation","start":140582957,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs866566926","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140582958,"strand":1,"feature_type":"variation","start":140582958,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140582960,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582960,"clinical_significance":[],"seq_region_name":"7","id":"rs368102933"},{"seq_region_name":"7","id":"rs2130637392","clinical_significance":[],"strand":1,"feature_type":"variation","end":140582961,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582961,"source":"dbSNP"},{"id":"rs1353729125","seq_region_name":"7","clinical_significance":[],"start":140582963,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140582963,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs762729275","seq_region_name":"7","feature_type":"variation","strand":1,"end":140582964,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582964},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140582967,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140582967,"clinical_significance":[],"seq_region_name":"7","id":"rs978875151"},{"end":140582974,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140582974,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585686117","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582982,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140582982,"id":"rs1264034934","seq_region_name":"7","clinical_significance":[]},{"end":140582990,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140582990,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1410469621"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140582995,"source":"dbSNP","strand":1,"feature_type":"variation","end":140582995,"alleles":["T","G"],"id":"rs1798604491","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140582997,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140582997,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798604607"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140583001,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583001,"clinical_significance":[],"seq_region_name":"7","id":"rs1443925350"},{"strand":1,"feature_type":"variation","end":140583004,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583004,"source":"dbSNP","seq_region_name":"7","id":"rs144915220","clinical_significance":[]},{"start":140583007,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140583007,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798604931","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798605039","clinical_significance":[],"start":140583011,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140583011,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs983479180","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583016,"source":"dbSNP","strand":1,"feature_type":"variation","end":140583016,"alleles":["G","A","T"]},{"seq_region_name":"7","id":"rs2130637489","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583019,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140583019},{"alleles":["G","C"],"end":140583020,"strand":1,"feature_type":"variation","start":140583020,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130637496","clinical_significance":[]},{"alleles":["G","A"],"end":140583021,"feature_type":"variation","strand":1,"source":"dbSNP","start":140583021,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1236761622"},{"strand":1,"feature_type":"variation","end":140583023,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583023,"source":"dbSNP","seq_region_name":"7","id":"rs1486171255","clinical_significance":[]},{"seq_region_name":"7","id":"rs955674388","clinical_significance":[],"alleles":["C","T"],"end":140583027,"strand":1,"feature_type":"variation","start":140583027,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140583029,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140583029,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1585686195","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140583030,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583030,"clinical_significance":[],"seq_region_name":"7","id":"rs992552287"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798605855","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583034,"feature_type":"variation","strand":1,"end":140583034,"alleles":["G","A"]},{"feature_type":"variation","strand":1,"end":140583037,"alleles":["AA","AAA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583036,"clinical_significance":[],"seq_region_name":"7","id":"rs1460211701"},{"id":"rs1798606080","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583040,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140583040},{"source":"dbSNP","start":140583041,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140583041,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1415163689"},{"start":140583042,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140583042,"alleles":["A","T"],"strand":1,"feature_type":"variation","id":"rs1798606258","seq_region_name":"7","clinical_significance":[]},{"start":140583043,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["ACAC","AC"],"end":140583046,"strand":1,"feature_type":"variation","id":"rs1186811135","seq_region_name":"7","clinical_significance":[]},{"id":"rs1798606486","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140583048,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583048,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1472623024","clinical_significance":[],"start":140583049,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140583049,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583051,"feature_type":"variation","strand":1,"end":140583051,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1798606670"},{"seq_region_name":"7","id":"rs1798606780","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583055,"source":"dbSNP","strand":1,"feature_type":"variation","end":140583055,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798606879","alleles":["C","G"],"end":140583056,"feature_type":"variation","strand":1,"source":"dbSNP","start":140583056,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs2130637616","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583057,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140583057},{"id":"rs1234156885","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140583058,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583058,"source":"dbSNP"},{"end":140583060,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140583060,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798607062","clinical_significance":[]},{"start":140583061,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140583061,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798607185","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs546863240","source":"dbSNP","start":140583062,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140583062,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1176697898","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583063,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140583063},{"strand":1,"feature_type":"variation","end":140583066,"alleles":["T","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583066,"source":"dbSNP","seq_region_name":"7","id":"rs960835719","clinical_significance":[]},{"end":140583069,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140583069,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs568762809"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583070,"source":"dbSNP","strand":1,"feature_type":"variation","end":140583070,"alleles":["T","C"],"seq_region_name":"7","id":"rs1798607869","clinical_significance":[]},{"seq_region_name":"7","id":"rs1272726035","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583071,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140583071},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140583072,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583072,"source":"dbSNP","seq_region_name":"7","id":"rs1798608105","clinical_significance":[]},{"end":140583073,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140583073,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1798608215","seq_region_name":"7"},{"start":140583074,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140583074,"alleles":["G","-"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1229295778","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583074,"source":"dbSNP","strand":1,"feature_type":"variation","end":140583074,"alleles":["G","A"],"seq_region_name":"7","id":"rs1798608317","clinical_significance":[]},{"seq_region_name":"7","id":"rs535769966","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583078,"source":"dbSNP","strand":1,"feature_type":"variation","end":140583078,"alleles":["T","A"]},{"source":"dbSNP","start":140583082,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140583082,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798608627"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798608750","end":140583085,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140583085,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1375583963","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583087,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140583087},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583088,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140583088,"clinical_significance":[],"seq_region_name":"7","id":"rs773914190"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583091,"source":"dbSNP","strand":1,"feature_type":"variation","end":140583091,"alleles":["A","T"],"seq_region_name":"7","id":"rs1798609089","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1441582506","end":140583092,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140583092,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["T","C"],"end":140583095,"feature_type":"variation","strand":1,"source":"dbSNP","start":140583095,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs759953905"},{"start":140583101,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140583101,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs909821790","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1460159613","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583107,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140583107},{"seq_region_name":"7","id":"rs1416458950","clinical_significance":[],"alleles":["G","A","C"],"end":140583108,"strand":1,"feature_type":"variation","start":140583108,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1798609663","seq_region_name":"7","feature_type":"variation","strand":1,"end":140583109,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583109},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583110,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140583110,"clinical_significance":[],"seq_region_name":"7","id":"rs1174410398"},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140583111,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583111,"clinical_significance":[],"seq_region_name":"7","id":"rs1163726675"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798609881","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583115,"feature_type":"variation","strand":1,"end":140583115,"alleles":["C","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1359058016","source":"dbSNP","start":140583115,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["CCCC","CCC","CCCCC"],"end":140583118,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798610131","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583116,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140583116},{"start":140583117,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140583117,"strand":1,"feature_type":"variation","id":"rs372048739","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140583118,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140583118,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1798610330","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs941282774","feature_type":"variation","strand":1,"end":140583119,"alleles":["A","C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583119},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140583124,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583124,"clinical_significance":[],"seq_region_name":"7","id":"rs976196502"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1300645454","source":"dbSNP","start":140583125,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140583125,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1798610851","seq_region_name":"7","source":"dbSNP","start":140583128,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140583128,"alleles":["A","T"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140583128,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AAAAAAAAAA","AAAAAAAAA","AAAAAAAAAAA"],"end":140583137,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs921977700"},{"feature_type":"variation","strand":1,"end":140583134,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583134,"clinical_significance":[],"id":"rs1798611269","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140583135,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583135,"clinical_significance":[],"id":"rs1798611439","seq_region_name":"7"},{"seq_region_name":"7","id":"rs2130637949","clinical_significance":[],"start":140583136,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140583136,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140583137,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140583137,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1037314880","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140583138,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583138,"source":"dbSNP","seq_region_name":"7","id":"rs1798611835","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140583139,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583139,"source":"dbSNP","seq_region_name":"7","id":"rs768123683","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs546951818","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583140,"feature_type":"variation","strand":1,"end":140583140,"alleles":["C","-"]},{"source":"dbSNP","start":140583140,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140583140,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798612232"},{"id":"rs1209583641","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140583142,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583142,"source":"dbSNP"},{"end":140583148,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140583148,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs897836150"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1275649068","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140583152,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583152},{"seq_region_name":"7","id":"rs752981936","clinical_significance":[],"start":140583153,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140583153,"strand":1,"feature_type":"variation"},{"id":"rs1585686548","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140583158,"alleles":["T","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583158,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1563157430","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583159,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140583159},{"source":"dbSNP","start":140583160,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140583160,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798613313"},{"seq_region_name":"7","id":"rs1585686566","clinical_significance":[],"strand":1,"feature_type":"variation","end":140583161,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583161,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140583162,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583162,"source":"dbSNP","seq_region_name":"7","id":"rs761066700","clinical_significance":[]},{"seq_region_name":"7","id":"rs1347415526","clinical_significance":[],"start":140583163,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C","G"],"end":140583163,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140583166,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583166,"clinical_significance":[],"seq_region_name":"7","id":"rs1798613780"},{"clinical_significance":[],"id":"rs1798613900","seq_region_name":"7","feature_type":"variation","strand":1,"end":140583199,"alleles":["CCCAGCTACTCGGGAGGCTGTAGTCCCAGCTAC","CCCAGCTAC"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583167},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140583173,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583173,"source":"dbSNP","id":"rs1345837355","seq_region_name":"7","clinical_significance":[]},{"start":140583175,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140583175,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs935574219","clinical_significance":[]},{"seq_region_name":"7","id":"rs527346872","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583177,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140583177},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583178,"feature_type":"variation","strand":1,"end":140583178,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs375838222"},{"clinical_significance":[],"id":"rs1798614520","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583180,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140583180},{"id":"rs1798614626","seq_region_name":"7","clinical_significance":[],"end":140583181,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140583181,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1317346415","clinical_significance":[],"start":140583183,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140583183,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1051865579","clinical_significance":[],"end":140583186,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140583186,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798614996","feature_type":"variation","strand":1,"end":140583191,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583191},{"clinical_significance":[],"seq_region_name":"7","id":"rs1052756577","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583193,"feature_type":"variation","strand":1,"end":140583193,"alleles":["C","A","T"]},{"alleles":["G","A"],"end":140583195,"feature_type":"variation","strand":1,"source":"dbSNP","start":140583195,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1321708644"},{"id":"rs1433337464","seq_region_name":"7","clinical_significance":[],"start":140583200,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140583200,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583209,"source":"dbSNP","strand":1,"feature_type":"variation","end":140583209,"alleles":["T","A"],"seq_region_name":"7","id":"rs2130638194","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140583210,"alleles":["G","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583210,"clinical_significance":[],"seq_region_name":"7","id":"rs1798615443"},{"strand":1,"feature_type":"variation","end":140583212,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583212,"source":"dbSNP","seq_region_name":"7","id":"rs890525225","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583215,"feature_type":"variation","strand":1,"end":140583215,"alleles":["A","C"],"clinical_significance":[],"id":"rs2130638216","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1315818515","source":"dbSNP","start":140583217,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140583217,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1399562939","clinical_significance":[],"strand":1,"feature_type":"variation","end":140583222,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583222,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140583224,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583224,"clinical_significance":[],"id":"rs1395209210","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140583225,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583225,"source":"dbSNP","seq_region_name":"7","id":"rs201691700","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1017769224","source":"dbSNP","start":140583226,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140583226,"alleles":["G","A","C"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140583228,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140583228,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130638259"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140583231,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583231,"clinical_significance":[],"seq_region_name":"7","id":"rs1283875904"},{"source":"dbSNP","start":140583233,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140583233,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs552169972"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1240526819","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583234,"feature_type":"variation","strand":1,"end":140583234,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1024070503","clinical_significance":[],"start":140583236,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140583236,"strand":1,"feature_type":"variation"},{"end":140583239,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140583239,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1000462437","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583240,"feature_type":"variation","strand":1,"end":140583240,"alleles":["T","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585686772"},{"alleles":["A","G"],"end":140583243,"feature_type":"variation","strand":1,"source":"dbSNP","start":140583243,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs570304351"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583246,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140583246,"clinical_significance":[],"seq_region_name":"7","id":"rs1798617082"},{"clinical_significance":[],"id":"rs1798617214","seq_region_name":"7","feature_type":"variation","strand":1,"end":140583247,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583247},{"clinical_significance":[],"seq_region_name":"7","id":"rs1282650188","feature_type":"variation","strand":1,"end":140583251,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583251},{"seq_region_name":"7","id":"rs2130638338","clinical_significance":[],"end":140583253,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140583253,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1232730637","clinical_significance":[],"alleles":["G","A"],"end":140583255,"strand":1,"feature_type":"variation","start":140583255,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140583257,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140583257,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs187775347"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140583258,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583258,"source":"dbSNP","seq_region_name":"7","id":"rs1298991786","clinical_significance":[]},{"alleles":["T","C"],"end":140583262,"feature_type":"variation","strand":1,"source":"dbSNP","start":140583262,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1476857404"},{"seq_region_name":"7","id":"rs549846116","clinical_significance":[],"start":140583263,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140583263,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs568013130","feature_type":"variation","strand":1,"end":140583265,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583265},{"id":"rs1798618167","seq_region_name":"7","clinical_significance":[],"start":140583267,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140583267,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583268,"source":"dbSNP","strand":1,"feature_type":"variation","end":140583268,"alleles":["C","T"],"id":"rs1420738717","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140583272,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140583272,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs535297323"},{"start":140583273,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140583273,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs191279218","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798618672","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140583278,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583278,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140583280,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583280,"source":"dbSNP","id":"rs1798618797","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798618904","source":"dbSNP","start":140583282,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140583282,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1024035130","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140583287,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583287,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583288,"feature_type":"variation","strand":1,"end":140583288,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs969771204"},{"source":"dbSNP","start":140583292,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140583296,"alleles":["GTACG","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1324317368"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1333000958","end":140583293,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140583293,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs572226292","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140583294,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583294},{"clinical_significance":[],"id":"rs980379933","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583295,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140583295},{"strand":1,"feature_type":"variation","end":140583296,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583296,"source":"dbSNP","seq_region_name":"7","id":"rs539521359","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583299,"source":"dbSNP","strand":1,"feature_type":"variation","end":140583299,"alleles":["A","T"],"id":"rs1186146583","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140583300,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583300,"clinical_significance":[],"id":"rs1798619999","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583303,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140583303,"seq_region_name":"7","id":"rs558137112","clinical_significance":[]},{"start":140583307,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140583307,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798620229","clinical_significance":[]},{"seq_region_name":"7","id":"rs760898302","clinical_significance":[],"alleles":["CAAACAAACAAACAAACAA","CAAACAAACAAACAA","CAAACAAACAAACAAACAAACAA","CAAACAAACAAACAAACAAACAAACAA"],"end":140583326,"strand":1,"feature_type":"variation","start":140583308,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140583312,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","-"],"end":140583312,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1283721771","clinical_significance":[]},{"source":"dbSNP","start":140583312,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140583312,"alleles":["C","A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1352899493"},{"seq_region_name":"7","id":"rs951976189","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583316,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140583316},{"end":140583335,"alleles":["CAAACAAACAAGCAAACAAA","CAAACAAA"],"strand":1,"feature_type":"variation","start":140583316,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1306094469","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583318,"source":"dbSNP","strand":1,"feature_type":"variation","end":140583318,"alleles":["A","G","T"],"seq_region_name":"7","id":"rs983364660","clinical_significance":[]},{"clinical_significance":[],"id":"rs1798621250","seq_region_name":"7","alleles":["A","G"],"end":140583319,"feature_type":"variation","strand":1,"source":"dbSNP","start":140583319,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs909717761","clinical_significance":[],"strand":1,"feature_type":"variation","end":140583320,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583320,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1798621492","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583322,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140583322},{"strand":1,"feature_type":"variation","end":140583324,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583324,"source":"dbSNP","id":"rs1291435476","seq_region_name":"7","clinical_significance":[]},{"id":"rs1798621731","seq_region_name":"7","clinical_significance":[],"end":140583330,"alleles":["CAAGCAA","CAAGCAAGCAA"],"strand":1,"feature_type":"variation","start":140583324,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1798621852","clinical_significance":[],"strand":1,"feature_type":"variation","end":140583325,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583325,"source":"dbSNP"},{"seq_region_name":"7","id":"rs757485645","clinical_significance":[],"end":140583326,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140583326,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["A","T"],"end":140583330,"feature_type":"variation","strand":1,"source":"dbSNP","start":140583330,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1412329817"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563157595","end":140583337,"alleles":["AAAAA","AAAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140583333,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140583348,"alleles":["AAAAAAA","AAAAAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140583342,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1354327816"},{"id":"rs1798622572","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583350,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140583350},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798622756","alleles":["AAA","AA"],"end":140583352,"feature_type":"variation","strand":1,"source":"dbSNP","start":140583350,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs941156581","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140583351,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583351},{"clinical_significance":[],"id":"rs576319907","seq_region_name":"7","feature_type":"variation","strand":1,"end":140583353,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583353},{"seq_region_name":"7","id":"rs976462227","clinical_significance":[],"end":140583354,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140583354,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583358,"source":"dbSNP","strand":1,"feature_type":"variation","end":140583358,"alleles":["T","G"],"seq_region_name":"7","id":"rs1169415672","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs918482501","end":140583359,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140583359,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1233169534","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583362,"feature_type":"variation","strand":1,"alleles":["T","-"],"end":140583362},{"source":"dbSNP","start":140583367,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140583367,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798623791"},{"id":"rs1798623952","seq_region_name":"7","clinical_significance":[],"start":140583371,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140583371,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"alleles":["A","G"],"end":140583374,"feature_type":"variation","strand":1,"source":"dbSNP","start":140583374,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs922060637"},{"alleles":["T","C"],"end":140583378,"strand":1,"feature_type":"variation","start":140583378,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs929314098","clinical_significance":[]},{"start":140583379,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140583379,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798624385","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583385,"source":"dbSNP","strand":1,"feature_type":"variation","end":140583385,"alleles":["G","T"],"seq_region_name":"7","id":"rs1798624496","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs979601964","feature_type":"variation","strand":1,"end":140583387,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583387},{"seq_region_name":"7","id":"rs1798624852","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140583395,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583395,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1474907157","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583402,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140583402},{"clinical_significance":[],"id":"rs925450298","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140583409,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583409},{"end":140583410,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140583410,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1179458868","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798625425","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140583411,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583411,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583418,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140583418,"clinical_significance":[],"seq_region_name":"7","id":"rs1439645451"},{"strand":1,"feature_type":"variation","end":140583419,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583419,"source":"dbSNP","seq_region_name":"7","id":"rs1051758796","clinical_significance":[]},{"clinical_significance":[],"id":"rs1214664049","seq_region_name":"7","feature_type":"variation","strand":1,"end":140583429,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583429},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798625889","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583429,"feature_type":"variation","strand":1,"end":140583430,"alleles":["GG","G"]},{"id":"rs1798626010","seq_region_name":"7","clinical_significance":[],"start":140583430,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140583430,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1164388608","end":140583431,"alleles":["A","AA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140583431,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140583431,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140583431,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798626180"},{"seq_region_name":"7","id":"rs568013460","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583432,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140583432},{"clinical_significance":[],"seq_region_name":"7","id":"rs890585547","alleles":["G","A"],"end":140583433,"feature_type":"variation","strand":1,"source":"dbSNP","start":140583433,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140583440,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140583440,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1231119469","clinical_significance":[]},{"source":"dbSNP","start":140583445,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140583445,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1798627091","seq_region_name":"7"},{"seq_region_name":"7","id":"rs2130638831","clinical_significance":[],"alleles":["G","A"],"end":140583446,"strand":1,"feature_type":"variation","start":140583446,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140583450,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140583450,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1320590779"},{"end":140583452,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140583452,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798627484"},{"feature_type":"variation","strand":1,"end":140583453,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583453,"clinical_significance":[],"id":"rs1307164003","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1392930244","clinical_significance":[],"start":140583456,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140583456,"alleles":["G","A","C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798628022","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583460,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140583460},{"clinical_significance":[],"seq_region_name":"7","id":"rs34576480","feature_type":"variation","strand":1,"end":140583463,"alleles":["GGGG","GGGGG"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583460},{"id":"rs1441297674","seq_region_name":"7","clinical_significance":[],"start":140583467,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140583467,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1403739146","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140583468,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583468},{"alleles":["C","G"],"end":140583471,"feature_type":"variation","strand":1,"source":"dbSNP","start":140583471,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798628437"},{"id":"rs943469435","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583472,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140583472},{"id":"rs778792406","seq_region_name":"7","clinical_significance":[],"start":140583473,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140583473,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798628801","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583479,"feature_type":"variation","strand":1,"end":140583479,"alleles":["A","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583480,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140583480,"id":"rs543794610","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798629002","source":"dbSNP","start":140583481,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140583481,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583483,"source":"dbSNP","strand":1,"feature_type":"variation","end":140583483,"alleles":["A","T"],"seq_region_name":"7","id":"rs1798629124","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583490,"feature_type":"variation","strand":1,"end":140583490,"alleles":["G","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1798629231"},{"alleles":["G","A"],"end":140583492,"feature_type":"variation","strand":1,"source":"dbSNP","start":140583492,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798629335"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583495,"source":"dbSNP","strand":1,"feature_type":"variation","end":140583499,"alleles":["AAAAA","AAAA","AAAAAA"],"seq_region_name":"7","id":"rs1461181812","clinical_significance":[]},{"seq_region_name":"7","id":"rs904705441","clinical_significance":[],"start":140583501,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140583501,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs992382157","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583502,"source":"dbSNP","strand":1,"feature_type":"variation","end":140583502,"alleles":["A","C"]},{"end":140583503,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140583503,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798629800"},{"id":"rs750583159","seq_region_name":"7","clinical_significance":[],"start":140583505,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140583505,"alleles":["T","A","G"],"strand":1,"feature_type":"variation"},{"id":"rs76515807","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583506,"source":"dbSNP","strand":1,"feature_type":"variation","end":140583506,"alleles":["C","A","T"]},{"seq_region_name":"7","id":"rs1798630240","clinical_significance":[],"start":140583507,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140583507,"alleles":["G","A","C"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140583510,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140583510,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798630474"},{"seq_region_name":"7","id":"rs1585687408","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140583517,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583517,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583519,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140583519,"clinical_significance":[],"seq_region_name":"7","id":"rs1194859556"},{"source":"dbSNP","start":140583520,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140583520,"alleles":["T","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1306852517"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583521,"feature_type":"variation","strand":1,"end":140583521,"alleles":["G","C"],"clinical_significance":[],"id":"rs1798631164","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1251597958","source":"dbSNP","start":140583523,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140583523,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583524,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140583524,"seq_region_name":"7","id":"rs1798631450","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs892036621","end":140583529,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140583529,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583530,"feature_type":"variation","strand":1,"end":140583530,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1798631878"},{"source":"dbSNP","start":140583532,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140583532,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1798632060","seq_region_name":"7"},{"end":140583535,"alleles":["GG","G"],"strand":1,"feature_type":"variation","start":140583534,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798632197","clinical_significance":[]},{"source":"dbSNP","start":140583538,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140583538,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798632373"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583539,"feature_type":"variation","strand":1,"end":140583539,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs948286469"},{"seq_region_name":"7","id":"rs1355144441","clinical_significance":[],"start":140583540,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140583540,"strand":1,"feature_type":"variation"},{"start":140583541,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140583541,"alleles":["C","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798632905","clinical_significance":[]},{"source":"dbSNP","start":140583542,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140583542,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585687475"},{"source":"dbSNP","start":140583543,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140583543,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1245402816"},{"seq_region_name":"7","id":"rs1013908030","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140583544,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583544,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585687490","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583546,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140583546},{"seq_region_name":"7","id":"rs1798633778","clinical_significance":[],"strand":1,"feature_type":"variation","end":140583552,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583552,"source":"dbSNP"},{"start":140583555,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140583555,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs974138580","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140583557,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583557,"clinical_significance":[],"seq_region_name":"7","id":"rs1798634104"},{"source":"dbSNP","start":140583571,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140583571,"alleles":["A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs550733306"},{"seq_region_name":"7","id":"rs1798634426","clinical_significance":[],"strand":1,"feature_type":"variation","end":140583579,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583579,"source":"dbSNP"},{"alleles":["A","C"],"end":140583584,"feature_type":"variation","strand":1,"source":"dbSNP","start":140583584,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1231786325"},{"alleles":["G","A","T"],"end":140583595,"strand":1,"feature_type":"variation","start":140583595,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1798634745","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583610,"source":"dbSNP","strand":1,"feature_type":"variation","end":140583610,"alleles":["A","C"],"seq_region_name":"7","id":"rs1798634953","clinical_significance":[]},{"source":"dbSNP","start":140583611,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140583611,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798635131"},{"source":"dbSNP","start":140583622,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140583622,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798635276"},{"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140583623,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583623,"clinical_significance":[],"id":"rs1353641512","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140583629,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583629,"source":"dbSNP","id":"rs1240509167","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1314633144","seq_region_name":"7","feature_type":"variation","strand":1,"end":140583631,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583631},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583632,"feature_type":"variation","strand":1,"end":140583632,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1798636014"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798636170","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583634,"feature_type":"variation","strand":1,"end":140583634,"alleles":["T","C"]},{"id":"rs574370829","seq_region_name":"7","clinical_significance":[],"end":140583635,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","start":140583635,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1798636549","seq_region_name":"7","clinical_significance":[],"start":140583637,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140583637,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583648,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140583648,"clinical_significance":[],"id":"rs1585687524","seq_region_name":"7"},{"seq_region_name":"7","id":"rs182977198","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583649,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140583649},{"start":140583651,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140583651,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs1258239432","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs559954993","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583652,"feature_type":"variation","strand":1,"end":140583652,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs187887720","clinical_significance":[],"alleles":["C","T"],"end":140583655,"strand":1,"feature_type":"variation","start":140583655,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs747923895","end":140583656,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140583656,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140583657,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140583657,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs192851849","seq_region_name":"7"},{"end":140583658,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140583658,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs564197215"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1048964306","source":"dbSNP","start":140583659,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140583659,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140583661,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583661,"source":"dbSNP","seq_region_name":"7","id":"rs1798638425","clinical_significance":[]},{"alleles":["G","A"],"end":140583662,"feature_type":"variation","strand":1,"source":"dbSNP","start":140583662,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1798638576","seq_region_name":"7"},{"seq_region_name":"7","id":"rs149058991","clinical_significance":[],"strand":1,"feature_type":"variation","end":140583667,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583667,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140583668,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583668,"clinical_significance":[],"seq_region_name":"7","id":"rs1798638936"},{"source":"dbSNP","start":140583669,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140583669,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1393827190"},{"id":"rs1798639285","seq_region_name":"7","clinical_significance":[],"start":140583671,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140583671,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140583672,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140583672,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1798639442","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583673,"feature_type":"variation","strand":1,"end":140583673,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs549730395"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583674,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140583674,"clinical_significance":[],"seq_region_name":"7","id":"rs986676301"},{"alleles":["C","T"],"end":140583676,"strand":1,"feature_type":"variation","start":140583676,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs568051033","clinical_significance":[]},{"end":140583678,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140583678,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1004685275"},{"start":140583679,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140583679,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1424550841","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583681,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140583681,"seq_region_name":"7","id":"rs1798640552","clinical_significance":[]},{"source":"dbSNP","start":140583686,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140583686,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1206575488"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583692,"feature_type":"variation","strand":1,"end":140583692,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1014857451"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798640871","source":"dbSNP","start":140583692,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140583693,"alleles":["GG","GGG"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140583695,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583695,"clinical_significance":[],"seq_region_name":"7","id":"rs1399238810"},{"feature_type":"variation","strand":1,"end":140583696,"alleles":["A","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583696,"clinical_significance":[],"seq_region_name":"7","id":"rs747401650"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583698,"feature_type":"variation","strand":1,"end":140583698,"alleles":["G","A"],"clinical_significance":[],"id":"rs1798641308","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1039139512","clinical_significance":[],"strand":1,"feature_type":"variation","end":140583699,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583699,"source":"dbSNP"},{"source":"dbSNP","start":140583700,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140583700,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs904589707"},{"end":140583701,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140583701,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1301164417","seq_region_name":"7"},{"source":"dbSNP","start":140583701,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140583703,"alleles":["GGG","GG"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798641764"},{"end":140583704,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140583704,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1338644138","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs529120268","seq_region_name":"7","alleles":["A","G"],"end":140583705,"feature_type":"variation","strand":1,"source":"dbSNP","start":140583705,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798642108","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583706,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140583706},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140583707,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583707,"clinical_significance":[],"seq_region_name":"7","id":"rs1563157849"},{"id":"rs1798642316","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140583708,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583708,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583709,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140583709,"clinical_significance":[],"seq_region_name":"7","id":"rs547212304"},{"clinical_significance":[],"id":"rs1798642584","seq_region_name":"7","source":"dbSNP","start":140583711,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140583711,"alleles":["C","G","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1264957157","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["-","TT"],"end":140583711,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583712,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs565491867","feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140583712,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583712},{"strand":1,"feature_type":"variation","end":140583713,"alleles":["A","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583713,"source":"dbSNP","seq_region_name":"7","id":"rs1216380149","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140583714,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583714,"clinical_significance":[],"seq_region_name":"7","id":"rs1257104692"},{"alleles":["T","G"],"end":140583716,"strand":1,"feature_type":"variation","start":140583716,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585687802","clinical_significance":[]},{"source":"dbSNP","start":140583718,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140583718,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1798643315","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1798643486","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583722,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140583722},{"seq_region_name":"7","id":"rs1339120426","clinical_significance":[],"start":140583723,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140583723,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs953500018","clinical_significance":[],"alleles":["T","C","G"],"end":140583724,"strand":1,"feature_type":"variation","start":140583724,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs576646346","seq_region_name":"7","alleles":["C","A","G","T"],"end":140583725,"feature_type":"variation","strand":1,"source":"dbSNP","start":140583725,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1475931390","seq_region_name":"7","source":"dbSNP","start":140583726,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140583726,"alleles":["G","A"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140583728,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583728,"clinical_significance":[],"id":"rs1798644571","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1585687879","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583729,"feature_type":"variation","strand":1,"end":140583729,"alleles":["A","C","G"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583730,"feature_type":"variation","strand":1,"alleles":["CCATCC","CC"],"end":140583735,"clinical_significance":[],"id":"rs1798644938","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583731,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140583731,"clinical_significance":[],"seq_region_name":"7","id":"rs1375180200"},{"strand":1,"feature_type":"variation","alleles":["ATCCTG","-"],"end":140583737,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583732,"source":"dbSNP","seq_region_name":"7","id":"rs1194870712","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","A","C","G"],"end":140583733,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583733,"clinical_significance":[],"seq_region_name":"7","id":"rs892083999"},{"end":140583735,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140583735,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1014459203","seq_region_name":"7"},{"id":"rs1426426375","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583736,"source":"dbSNP","strand":1,"feature_type":"variation","end":140583736,"alleles":["T","C"]},{"source":"dbSNP","start":140583737,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["-","A"],"end":140583736,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798646077"},{"end":140583737,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140583737,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1486379846","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798646397","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583737,"feature_type":"variation","strand":1,"alleles":["G","GG"],"end":140583737},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798646548","feature_type":"variation","strand":1,"alleles":["GTG","-"],"end":140583739,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583737},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583738,"feature_type":"variation","strand":1,"alleles":["-","AC","C","GC","GT"],"end":140583737,"clinical_significance":[],"seq_region_name":"7","id":"rs751846011"},{"end":140583739,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140583739,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1441220361","clinical_significance":[]},{"start":140583740,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["-","GCTAA"],"end":140583739,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798647067","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798647174","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583740,"source":"dbSNP","strand":1,"feature_type":"variation","end":140583740,"alleles":["A","C"]},{"clinical_significance":[],"id":"rs1298903320","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583741,"feature_type":"variation","strand":1,"end":140583740,"alleles":["-","C","G","GCTAAC"]},{"source":"dbSNP","start":140583741,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140583741,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1798647440","seq_region_name":"7"},{"alleles":["A","ACA"],"end":140583741,"strand":1,"feature_type":"variation","start":140583741,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798647537","clinical_significance":[]},{"start":140583742,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A","C","G"],"end":140583742,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs539931873","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583743,"source":"dbSNP","strand":1,"feature_type":"variation","end":140583743,"alleles":["G","A"],"id":"rs1252918066","seq_region_name":"7","clinical_significance":[]},{"alleles":["GG","G"],"end":140583744,"strand":1,"feature_type":"variation","start":140583743,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1798647937","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1024475601","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583748,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140583748},{"alleles":["A","C"],"end":140583749,"feature_type":"variation","strand":1,"source":"dbSNP","start":140583749,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585688029"},{"id":"rs925335063","seq_region_name":"7","clinical_significance":[],"start":140583750,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","T"],"end":140583750,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1798648425","clinical_significance":[],"alleles":["CCCC","CCC"],"end":140583753,"strand":1,"feature_type":"variation","start":140583750,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583751,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140583751,"clinical_significance":[],"seq_region_name":"7","id":"rs1585688046"},{"start":140583752,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140583752,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1263975282","clinical_significance":[]},{"seq_region_name":"7","id":"rs1294174494","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583753,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140583753},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583754,"feature_type":"variation","strand":1,"end":140583754,"alleles":["G","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs184829422"},{"source":"dbSNP","start":140583754,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140583755,"alleles":["GT","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130639839"},{"source":"dbSNP","start":140583755,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140583755,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs188909609","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1001584150","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583756,"feature_type":"variation","strand":1,"alleles":["C","A","G","T"],"end":140583756},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583757,"source":"dbSNP","strand":1,"feature_type":"variation","end":140583757,"alleles":["T","C"],"seq_region_name":"7","id":"rs956880782","clinical_significance":[]},{"clinical_significance":[],"id":"rs1413202563","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140583758,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583758},{"clinical_significance":[],"seq_region_name":"7","id":"rs541256796","source":"dbSNP","start":140583759,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140583759,"feature_type":"variation","strand":1},{"id":"rs1798649717","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140583760,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583760,"source":"dbSNP"},{"start":140583762,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140583762,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","id":"rs1411080156","seq_region_name":"7","clinical_significance":[]},{"end":140583763,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140583763,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs537083124","clinical_significance":[]},{"source":"dbSNP","start":140583765,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140583765,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1798650063","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140583766,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583766,"clinical_significance":[],"id":"rs1166456385","seq_region_name":"7"},{"start":140583770,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140583770,"alleles":["C","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130639919","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583771,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AAAAAA","AAAAAAA"],"end":140583776,"seq_region_name":"7","id":"rs1423256357","clinical_significance":[]},{"clinical_significance":[],"id":"rs2130639939","seq_region_name":"7","source":"dbSNP","start":140583776,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140583776,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1466310232","seq_region_name":"7","end":140583777,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140583777,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1422421219","seq_region_name":"7","clinical_significance":[],"end":140583778,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140583778,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs962762986","clinical_significance":[],"strand":1,"feature_type":"variation","end":140583781,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583781,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1174110899","clinical_significance":[],"start":140583782,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140583782,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs994041780","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583783,"source":"dbSNP","strand":1,"feature_type":"variation","end":140583783,"alleles":["A","G"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583786,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140583786,"seq_region_name":"7","id":"rs1025486197","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140583787,"alleles":["G","A","C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583787,"source":"dbSNP","seq_region_name":"7","id":"rs1395359606","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1193821795","end":140583788,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140583788,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583789,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140583789,"clinical_significance":[],"seq_region_name":"7","id":"rs1317097684"},{"end":140583790,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140583790,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs955157803"},{"strand":1,"feature_type":"variation","end":140583790,"alleles":["-","CA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583791,"source":"dbSNP","seq_region_name":"7","id":"rs1798651421","clinical_significance":[]},{"seq_region_name":"7","id":"rs1298775704","clinical_significance":[],"strand":1,"feature_type":"variation","end":140583791,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583791,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140583792,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583792,"clinical_significance":[],"seq_region_name":"7","id":"rs986729668"},{"strand":1,"feature_type":"variation","alleles":["GG","-"],"end":140583793,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583792,"source":"dbSNP","id":"rs1798651748","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1798651845","seq_region_name":"7","alleles":["GCG","G"],"end":140583795,"feature_type":"variation","strand":1,"source":"dbSNP","start":140583793,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140583794,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583794,"source":"dbSNP","seq_region_name":"7","id":"rs573635153","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs574715088","alleles":["G","A"],"end":140583795,"feature_type":"variation","strand":1,"source":"dbSNP","start":140583795,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1798652199","clinical_significance":[],"strand":1,"feature_type":"variation","end":140583797,"alleles":["GGG","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583795,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583796,"feature_type":"variation","strand":1,"end":140583796,"alleles":["G","C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1397656587"},{"clinical_significance":[],"id":"rs1585688332","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583797,"feature_type":"variation","strand":1,"end":140583797,"alleles":["G","A"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583798,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140583798,"seq_region_name":"7","id":"rs975138146","clinical_significance":[]},{"alleles":["G","A"],"end":140583799,"strand":1,"feature_type":"variation","start":140583799,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs926095152","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1327472755","feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140583803,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583803},{"seq_region_name":"7","id":"rs1277111763","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583806,"source":"dbSNP","strand":1,"feature_type":"variation","end":140583806,"alleles":["G","T"]},{"end":140583807,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","start":140583807,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs918198386","clinical_significance":[]},{"seq_region_name":"7","id":"rs936079996","clinical_significance":[],"start":140583809,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140583809,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583816,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140583816,"seq_region_name":"7","id":"rs1165188717","clinical_significance":[]},{"end":140583818,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140583818,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs866363449"},{"clinical_significance":[],"seq_region_name":"7","id":"rs913407648","feature_type":"variation","strand":1,"end":140583819,"alleles":["G","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583819},{"seq_region_name":"7","id":"rs1162053640","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140583820,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583820,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs950189972","end":140583821,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140583821,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140583822,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140583822,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1045434671"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583831,"source":"dbSNP","strand":1,"feature_type":"variation","end":140583831,"alleles":["C","A"],"seq_region_name":"7","id":"rs1179642845","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583832,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140583832,"clinical_significance":[],"seq_region_name":"7","id":"rs1234365653"},{"seq_region_name":"7","id":"rs1258153446","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140583833,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583833,"source":"dbSNP"},{"source":"dbSNP","start":140583835,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140583835,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1467267392"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130640235","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140583839,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583839},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130640240","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583841,"feature_type":"variation","strand":1,"end":140583841,"alleles":["G","A"]},{"feature_type":"variation","strand":1,"end":140583842,"alleles":["C","A","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583842,"clinical_significance":[],"seq_region_name":"7","id":"rs1343377331"},{"id":"rs1210763961","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583843,"source":"dbSNP","strand":1,"feature_type":"variation","end":140583843,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1287449101","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583845,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140583845},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583850,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140583850,"seq_region_name":"7","id":"rs1489306778","clinical_significance":[]},{"seq_region_name":"7","id":"rs574407819","clinical_significance":[],"alleles":["G","A"],"end":140583852,"strand":1,"feature_type":"variation","start":140583852,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140583853,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583853,"source":"dbSNP","seq_region_name":"7","id":"rs1798654896","clinical_significance":[]},{"seq_region_name":"7","id":"rs1191615709","clinical_significance":[],"end":140583857,"alleles":["T","C","G"],"strand":1,"feature_type":"variation","start":140583857,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs2130640295","clinical_significance":[],"end":140583858,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140583858,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1798655140","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140583861,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583861},{"seq_region_name":"7","id":"rs1261222815","clinical_significance":[],"strand":1,"feature_type":"variation","end":140583862,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583862,"source":"dbSNP"},{"id":"rs1585688538","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140583863,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583863,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1798655475","clinical_significance":[],"start":140583865,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140583865,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1798655590","clinical_significance":[],"end":140583866,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140583866,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1434015189","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140583868,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583868,"source":"dbSNP"},{"seq_region_name":"7","id":"rs2130640343","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583869,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140583869},{"clinical_significance":[],"id":"rs1372163710","seq_region_name":"7","end":140583870,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140583870,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140583873,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140583873,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130640363","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583874,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140583874,"clinical_significance":[],"seq_region_name":"7","id":"rs541696547"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140583875,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583875,"source":"dbSNP","id":"rs553612000","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs936951219","clinical_significance":[],"start":140583876,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140583876,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583877,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140583877,"clinical_significance":[],"seq_region_name":"7","id":"rs1798656349"},{"id":"rs1433939123","seq_region_name":"7","clinical_significance":[],"end":140583879,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","start":140583879,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1159166852","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583880,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140583880},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583881,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140583881,"seq_region_name":"7","id":"rs1362387580","clinical_significance":[]},{"seq_region_name":"7","id":"rs192167702","clinical_significance":[],"strand":1,"feature_type":"variation","end":140583882,"alleles":["T","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583882,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1798657010","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583883,"feature_type":"variation","strand":1,"end":140583883,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1048850712","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583886,"feature_type":"variation","strand":1,"end":140583886,"alleles":["A","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1476937581","end":140583887,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140583887,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs545579225","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583889,"feature_type":"variation","strand":1,"end":140583889,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1798657449","clinical_significance":[],"start":140583890,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140583890,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583891,"source":"dbSNP","strand":1,"feature_type":"variation","end":140583891,"alleles":["A","T"],"id":"rs1798657559","seq_region_name":"7","clinical_significance":[]},{"start":140583892,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G","T"],"end":140583892,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1246296107","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1390940136","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583896,"feature_type":"variation","strand":1,"end":140583896,"alleles":["A","C","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1282316582","alleles":["G","A"],"end":140583897,"feature_type":"variation","strand":1,"source":"dbSNP","start":140583897,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140583900,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140583900,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs564056506","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs531421721","clinical_significance":[],"start":140583901,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140583901,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140583904,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583904,"clinical_significance":[],"seq_region_name":"7","id":"rs11972091"},{"clinical_significance":[],"id":"rs561323099","seq_region_name":"7","source":"dbSNP","start":140583905,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140583905,"alleles":["G","A","C"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140583907,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140583907,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs369041194"},{"clinical_significance":[],"seq_region_name":"7","id":"rs74672715","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583908,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140583908},{"feature_type":"variation","strand":1,"end":140583909,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583909,"clinical_significance":[],"seq_region_name":"7","id":"rs1798658804"},{"feature_type":"variation","strand":1,"end":140583911,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583911,"clinical_significance":[],"seq_region_name":"7","id":"rs529153887"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583912,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140583912,"clinical_significance":[],"seq_region_name":"7","id":"rs1329711080"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1431101179","alleles":["A","G"],"end":140583913,"feature_type":"variation","strand":1,"source":"dbSNP","start":140583913,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["ACTCCGTCTCGAAAAA","A"],"end":140583931,"strand":1,"feature_type":"variation","start":140583916,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798659286","clinical_significance":[]},{"seq_region_name":"7","id":"rs1346444030","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140583917,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583917,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585688784","end":140583920,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140583920,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140583921,"alleles":["G","GG"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583921,"source":"dbSNP","seq_region_name":"7","id":"rs1295750708","clinical_significance":[]},{"start":140583921,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140583921,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1418567770","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583925,"source":"dbSNP","strand":1,"feature_type":"variation","end":140583925,"alleles":["C","A","T"],"seq_region_name":"7","id":"rs1798659889","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798659995","source":"dbSNP","start":140583925,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140583926,"alleles":["CG","-"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583926,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["-","A","CA"],"end":140583925,"seq_region_name":"7","id":"rs1798660099","clinical_significance":[]},{"start":140583926,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140583926,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","id":"rs868732246","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1175465057","feature_type":"variation","strand":1,"end":140583926,"alleles":["G","GG"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583926},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583926,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","-"],"end":140583926,"seq_region_name":"7","id":"rs1431208378","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1554473822","feature_type":"variation","strand":1,"end":140583926,"alleles":["-","GA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583927},{"clinical_significance":[],"id":"rs2130640643","seq_region_name":"7","feature_type":"variation","strand":1,"end":140583927,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583927},{"clinical_significance":[],"seq_region_name":"7","id":"rs35931795","source":"dbSNP","start":140583927,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140583941,"alleles":["AAAAAAAAAAAAAAA","AAAAAAAAAAA","AAAAAAAAAAAAA","AAAAAAAAAAAAAA","AAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAA"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1585688872","clinical_significance":[],"start":140583931,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140583931,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"end":140583931,"alleles":["-","C","CAAAAAC"],"strand":1,"feature_type":"variation","start":140583932,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1425373052","clinical_significance":[]},{"end":140583932,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140583932,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1310561055","clinical_significance":[]},{"start":140583935,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","AGA"],"end":140583935,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1208686664","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130640717","end":140583937,"alleles":["AA","AACAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140583936,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140583936,"alleles":["-","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583937,"clinical_significance":[],"seq_region_name":"7","id":"rs1214493910"},{"seq_region_name":"7","id":"rs1260243824","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140583937,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583937,"source":"dbSNP"},{"source":"dbSNP","start":140583938,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140583937,"alleles":["-","CAACAACAAC"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130640745"},{"strand":1,"feature_type":"variation","end":140583938,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583938,"source":"dbSNP","seq_region_name":"7","id":"rs1488870593","clinical_significance":[]},{"seq_region_name":"7","id":"rs1311974622","clinical_significance":[],"start":140583941,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140583941,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798661992","end":140583941,"alleles":["-","AAT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140583942,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585688951","feature_type":"variation","strand":1,"end":140583942,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583942},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798662225","end":140583943,"alleles":["GT","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140583942,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1585688959","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583943,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","C","G"],"end":140583943},{"strand":1,"feature_type":"variation","alleles":["-","AAA"],"end":140583943,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583944,"source":"dbSNP","seq_region_name":"7","id":"rs1798662504","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140583944,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583944,"source":"dbSNP","seq_region_name":"7","id":"rs1585688976","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798662727","clinical_significance":[],"start":140583947,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140583947,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"id":"rs1798662843","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140583951,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583951,"source":"dbSNP"},{"alleles":["T","C"],"end":140583956,"strand":1,"feature_type":"variation","start":140583956,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798662963","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs887497733","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583960,"feature_type":"variation","strand":1,"alleles":["G","C","T"],"end":140583960},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585688992","alleles":["T","G"],"end":140583962,"feature_type":"variation","strand":1,"source":"dbSNP","start":140583962,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1585689004","seq_region_name":"7","clinical_significance":[],"end":140583966,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140583966,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140583967,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140583967,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1585689014","seq_region_name":"7"},{"id":"rs269236","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","G","T"],"end":140583969,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583969,"source":"dbSNP"},{"seq_region_name":"7","id":"rs374857242","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583970,"source":"dbSNP","strand":1,"feature_type":"variation","end":140583970,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs2130640884","clinical_significance":[],"strand":1,"feature_type":"variation","end":140583971,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583971,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583972,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140583972,"seq_region_name":"7","id":"rs1001236136","clinical_significance":[]},{"end":140583973,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140583973,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1355597040"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798664252","feature_type":"variation","strand":1,"alleles":["CTCAC","CTCACTCAC"],"end":140583979,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583975},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140583976,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583976,"clinical_significance":[],"seq_region_name":"7","id":"rs1038435953"},{"feature_type":"variation","strand":1,"end":140583977,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583977,"clinical_significance":[],"seq_region_name":"7","id":"rs1464533620"},{"clinical_significance":[],"id":"rs1004737768","seq_region_name":"7","source":"dbSNP","start":140583978,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140583978,"feature_type":"variation","strand":1},{"alleles":["C","G","T"],"end":140583979,"strand":1,"feature_type":"variation","start":140583979,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1036587825","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140583980,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583980,"source":"dbSNP","seq_region_name":"7","id":"rs898122752","clinical_significance":[]},{"alleles":["C","T"],"end":140583982,"strand":1,"feature_type":"variation","start":140583982,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1158353052","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583984,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140583984,"seq_region_name":"7","id":"rs1798665098","clinical_significance":[]},{"source":"dbSNP","start":140583985,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A","C"],"end":140583985,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs866698789","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583988,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140583988,"id":"rs1585689152","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798665484","end":140583989,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140583989,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1475555945","source":"dbSNP","start":140583989,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["CC","C"],"end":140583990,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798665722","end":140583990,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140583990,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs993927267","alleles":["T","C"],"end":140583991,"feature_type":"variation","strand":1,"source":"dbSNP","start":140583991,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140583992,"feature_type":"variation","strand":1,"end":140583992,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs269237"},{"seq_region_name":"7","id":"rs1798666129","clinical_significance":[],"strand":1,"feature_type":"variation","end":140583994,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140583994,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140584000,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584000,"clinical_significance":[],"seq_region_name":"7","id":"rs1483178373"},{"seq_region_name":"7","id":"rs1233974497","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584004,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140584004},{"source":"dbSNP","start":140584004,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["GG","G"],"end":140584005,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130641031"},{"source":"dbSNP","start":140584005,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140584005,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1207018218"},{"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140584007,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584007,"source":"dbSNP","seq_region_name":"7","id":"rs1316472261","clinical_significance":[]},{"seq_region_name":"7","id":"rs955212226","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584008,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140584008},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798666791","end":140584009,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140584009,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["G","A"],"end":140584011,"feature_type":"variation","strand":1,"source":"dbSNP","start":140584011,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798666881"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1291420741","feature_type":"variation","strand":1,"end":140584012,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584012},{"clinical_significance":[],"seq_region_name":"7","id":"rs1008048467","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584013,"feature_type":"variation","strand":1,"end":140584013,"alleles":["G","A","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584015,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140584015,"clinical_significance":[],"seq_region_name":"7","id":"rs1294531865"},{"source":"dbSNP","start":140584016,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140584016,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1018222151"},{"start":140584017,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140584017,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs530896227","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798667586","clinical_significance":[],"strand":1,"feature_type":"variation","end":140584018,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584018,"source":"dbSNP"},{"alleles":["A","C","G"],"end":140584019,"feature_type":"variation","strand":1,"source":"dbSNP","start":140584019,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs997838385"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584020,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140584020,"clinical_significance":[],"seq_region_name":"7","id":"rs1798667827"},{"strand":1,"feature_type":"variation","end":140584021,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584021,"source":"dbSNP","seq_region_name":"7","id":"rs974808558","clinical_significance":[]},{"end":140584024,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140584024,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1379699365","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584024,"feature_type":"variation","strand":1,"end":140584025,"alleles":["TT","-"],"clinical_significance":[],"seq_region_name":"7","id":"rs1798668178"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584028,"source":"dbSNP","strand":1,"feature_type":"variation","end":140584028,"alleles":["G","A"],"seq_region_name":"7","id":"rs1028868480","clinical_significance":[]},{"clinical_significance":[],"id":"rs1585689364","seq_region_name":"7","source":"dbSNP","start":140584030,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140584030,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584031,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140584031,"clinical_significance":[],"id":"rs1798668517","seq_region_name":"7"},{"seq_region_name":"7","id":"rs533006325","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584033,"source":"dbSNP","strand":1,"feature_type":"variation","end":140584033,"alleles":["G","A"]},{"alleles":["G","A"],"end":140584036,"strand":1,"feature_type":"variation","start":140584036,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1420314690","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584037,"feature_type":"variation","strand":1,"end":140584037,"alleles":["T","G"],"clinical_significance":[],"id":"rs1585689401","seq_region_name":"7"},{"id":"rs925947104","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140584039,"strand":1,"feature_type":"variation","start":140584039,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["C","A"],"end":140584044,"feature_type":"variation","strand":1,"source":"dbSNP","start":140584044,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585689411"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584045,"feature_type":"variation","strand":1,"end":140584045,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1238585062"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584047,"source":"dbSNP","strand":1,"feature_type":"variation","end":140584047,"alleles":["G","T"],"seq_region_name":"7","id":"rs367701785","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798669382","clinical_significance":[],"end":140584048,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140584048,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["-","T"],"end":140584048,"feature_type":"variation","strand":1,"source":"dbSNP","start":140584049,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1409295158"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584051,"source":"dbSNP","strand":1,"feature_type":"variation","end":140584051,"alleles":["G","C"],"id":"rs1179515346","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs957331207","clinical_significance":[],"strand":1,"feature_type":"variation","end":140584052,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584052,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1238024806","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584053,"feature_type":"variation","strand":1,"end":140584053,"alleles":["C","T"]},{"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140584054,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584054,"source":"dbSNP","seq_region_name":"7","id":"rs371875946","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584055,"source":"dbSNP","strand":1,"feature_type":"variation","end":140584055,"alleles":["A","T"],"seq_region_name":"7","id":"rs1214720503","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140584056,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584056,"source":"dbSNP","seq_region_name":"7","id":"rs1798670197","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs988866444","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584057,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140584057},{"clinical_significance":[],"seq_region_name":"7","id":"rs184901811","end":140584058,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140584058,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140584059,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584059,"source":"dbSNP","seq_region_name":"7","id":"rs375219132","clinical_significance":[]},{"id":"rs1468225081","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584062,"source":"dbSNP","strand":1,"feature_type":"variation","end":140584062,"alleles":["T","A"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584064,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AAA","AA"],"end":140584066,"seq_region_name":"7","id":"rs1198986295","clinical_significance":[]},{"seq_region_name":"7","id":"rs1000791159","clinical_significance":[],"start":140584067,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140584067,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140584068,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140584068,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs189621598"},{"end":140584070,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140584070,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1374370880"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140584071,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584071,"clinical_significance":[],"seq_region_name":"7","id":"rs141297967"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140584072,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584072,"clinical_significance":[],"seq_region_name":"7","id":"rs1585689574"},{"id":"rs927601437","seq_region_name":"7","clinical_significance":[],"start":140584073,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140584073,"alleles":["C","A","G"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584074,"feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140584074,"clinical_significance":[],"seq_region_name":"7","id":"rs1798671724"},{"start":140584077,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140584077,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798671866","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798671997","clinical_significance":[],"end":140584080,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140584080,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140584084,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140584084,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs937593289","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798672209","source":"dbSNP","start":140584085,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140584085,"alleles":["T","C"],"feature_type":"variation","strand":1},{"end":140584086,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140584086,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1798672320","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["A","C","T"],"end":140584089,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584089,"source":"dbSNP","id":"rs1798672804","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","C"],"end":140584091,"feature_type":"variation","strand":1,"source":"dbSNP","start":140584091,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1396915309"},{"seq_region_name":"7","id":"rs1798673042","clinical_significance":[],"alleles":["A","G"],"end":140584092,"strand":1,"feature_type":"variation","start":140584092,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140584096,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140584096,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798673157"},{"start":140584098,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140584098,"strand":1,"feature_type":"variation","id":"rs1798673281","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs537939310","seq_region_name":"7","end":140584099,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140584099,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","T"],"end":140584102,"strand":1,"feature_type":"variation","start":140584102,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1798673506","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs567621003","clinical_significance":[],"start":140584103,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140584103,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1798673735","clinical_significance":[],"start":140584107,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140584107,"strand":1,"feature_type":"variation"},{"start":140584110,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140584110,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs535004302","clinical_significance":[]},{"alleles":["G","A"],"end":140584111,"feature_type":"variation","strand":1,"source":"dbSNP","start":140584111,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs553748083"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798674095","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584112,"feature_type":"variation","strand":1,"end":140584112,"alleles":["C","T"]},{"feature_type":"variation","strand":1,"end":140584113,"alleles":["A","C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584113,"clinical_significance":[],"seq_region_name":"7","id":"rs890868744"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584114,"feature_type":"variation","strand":1,"end":140584114,"alleles":["T","C"],"clinical_significance":[],"id":"rs1433069656","seq_region_name":"7"},{"id":"rs1798674449","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584116,"source":"dbSNP","strand":1,"feature_type":"variation","end":140584116,"alleles":["C","G"]},{"id":"rs1438319451","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140584118,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584118,"source":"dbSNP"},{"start":140584122,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140584122,"alleles":["A","C","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs796425160","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584123,"source":"dbSNP","strand":1,"feature_type":"variation","end":140584123,"alleles":["T","A"],"id":"rs988355383","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs180805531","source":"dbSNP","start":140584124,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140584124,"alleles":["C","T"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140584126,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584126,"source":"dbSNP","seq_region_name":"7","id":"rs1268989948","clinical_significance":[]},{"clinical_significance":[],"id":"rs1798675168","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584129,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140584129},{"clinical_significance":[],"seq_region_name":"7","id":"rs1403350832","end":140584132,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140584132,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs367891277","source":"dbSNP","start":140584133,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140584133,"alleles":["T","C"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140584137,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584137,"source":"dbSNP","seq_region_name":"7","id":"rs1018523794","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584139,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140584139,"clinical_significance":[],"seq_region_name":"7","id":"rs1798675625"},{"feature_type":"variation","strand":1,"end":140584140,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584140,"clinical_significance":[],"seq_region_name":"7","id":"rs2130641580"},{"source":"dbSNP","start":140584141,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140584141,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1798675734","seq_region_name":"7"},{"clinical_significance":[],"id":"rs372128332","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140584143,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584143},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585689764","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584144,"feature_type":"variation","strand":1,"end":140584144,"alleles":["A","G"]},{"id":"rs971042603","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584146,"source":"dbSNP","strand":1,"feature_type":"variation","end":140584146,"alleles":["G","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs186203431","feature_type":"variation","strand":1,"end":140584155,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584155},{"seq_region_name":"7","id":"rs113926045","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584156,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140584156},{"seq_region_name":"7","id":"rs1798676418","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584157,"source":"dbSNP","strand":1,"feature_type":"variation","end":140584157,"alleles":["G","C"]},{"start":140584159,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A","G"],"end":140584159,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs113321702","clinical_significance":[]},{"end":140584160,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140584160,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1798676670","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140584161,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584161,"source":"dbSNP","seq_region_name":"7","id":"rs1798676756","clinical_significance":[]},{"source":"dbSNP","start":140584163,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140584163,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798676863"},{"id":"rs1798676964","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584164,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140584164},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140584165,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584165,"clinical_significance":[],"id":"rs1332662557","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584166,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140584166,"id":"rs78842802","seq_region_name":"7","clinical_significance":[]},{"start":140584167,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140584167,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1380533691","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585689839","clinical_significance":[],"alleles":["T","G"],"end":140584173,"strand":1,"feature_type":"variation","start":140584173,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140584176,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140584176,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798677583"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798677692","alleles":["G","A","T"],"end":140584177,"feature_type":"variation","strand":1,"source":"dbSNP","start":140584177,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584182,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140584182,"clinical_significance":[],"id":"rs1032230133","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140584183,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584183,"clinical_significance":[],"id":"rs1798677952","seq_region_name":"7"},{"id":"rs112539224","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140584184,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584184,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1798678233","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584186,"source":"dbSNP","strand":1,"feature_type":"variation","end":140584186,"alleles":["G","A","T"]},{"start":140584189,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140584189,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1174868410","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs543066895","feature_type":"variation","strand":1,"end":140584190,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584190},{"seq_region_name":"7","id":"rs1376348542","clinical_significance":[],"start":140584191,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140584191,"alleles":["G","A","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798678725","source":"dbSNP","start":140584193,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140584193,"alleles":["G","C"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140584195,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584195,"source":"dbSNP","seq_region_name":"7","id":"rs1585689903","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1196285383","source":"dbSNP","start":140584196,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140584196,"alleles":["T","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1798679045","clinical_significance":[],"start":140584196,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140584199,"alleles":["TGTG","TG"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140584198,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140584198,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1020353639","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140584202,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584202,"clinical_significance":[],"seq_region_name":"7","id":"rs1262004376"},{"seq_region_name":"7","id":"rs1195165706","clinical_significance":[],"end":140584207,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140584207,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140584210,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584210,"clinical_significance":[],"seq_region_name":"7","id":"rs1798679368"},{"seq_region_name":"7","id":"rs1798679462","clinical_significance":[],"strand":1,"feature_type":"variation","end":140584211,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584211,"source":"dbSNP"},{"end":140584215,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140584215,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798679579"},{"strand":1,"feature_type":"variation","end":140584217,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584217,"source":"dbSNP","seq_region_name":"7","id":"rs1798679719","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798679829","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140584220,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584220},{"seq_region_name":"7","id":"rs1487037015","clinical_significance":[],"strand":1,"feature_type":"variation","end":140584222,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584222,"source":"dbSNP"},{"id":"rs774082088","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584228,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140584228},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584233,"feature_type":"variation","strand":1,"end":140584233,"alleles":["C","T"],"clinical_significance":[],"id":"rs556337034","seq_region_name":"7"},{"end":140584236,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140584236,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs981672725"},{"seq_region_name":"7","id":"rs1334322813","clinical_significance":[],"start":140584237,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140584237,"strand":1,"feature_type":"variation"},{"alleles":["AAAAACAAAAACAAAAA","AAAAACAAAAACAAAAACAAAAA"],"end":140584259,"feature_type":"variation","strand":1,"source":"dbSNP","start":140584243,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798680564"},{"id":"rs940410804","seq_region_name":"7","clinical_significance":[],"start":140584246,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140584246,"alleles":["A","C","G","T"],"strand":1,"feature_type":"variation"},{"alleles":["AAAAA","AAAA"],"end":140584253,"feature_type":"variation","strand":1,"source":"dbSNP","start":140584249,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1563158438"},{"seq_region_name":"7","id":"rs1798680937","clinical_significance":[],"start":140584254,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140584254,"strand":1,"feature_type":"variation"},{"end":140584255,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140584255,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1219443198","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1798681161","clinical_significance":[],"strand":1,"feature_type":"variation","end":140584260,"alleles":["AAAAAA","AAAAA","AAAAAAAAAAAA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584255,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140584258,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584258,"source":"dbSNP","seq_region_name":"7","id":"rs1398202141","clinical_significance":[]},{"alleles":["AACAACAACAACAA","AACAACAACAA"],"end":140584272,"feature_type":"variation","strand":1,"source":"dbSNP","start":140584259,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1036235055"},{"clinical_significance":[],"seq_region_name":"7","id":"rs927461896","feature_type":"variation","strand":1,"end":140584260,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584260},{"alleles":["C","T"],"end":140584264,"strand":1,"feature_type":"variation","start":140584264,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798681652","clinical_significance":[]},{"seq_region_name":"7","id":"rs937496454","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140584268,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584268,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140584272,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584272,"clinical_significance":[],"id":"rs1798681858","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1398360786","clinical_significance":[],"end":140584274,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140584274,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140584275,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584275,"source":"dbSNP","id":"rs901673010","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140584276,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140584276,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs974750388"},{"id":"rs1798682483","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140584277,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584277,"source":"dbSNP"},{"end":140584279,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140584279,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798682579"},{"clinical_significance":[],"seq_region_name":"7","id":"rs933132379","feature_type":"variation","strand":1,"end":140584280,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584280},{"start":140584281,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140584281,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1462846831","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140584288,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584288,"source":"dbSNP","seq_region_name":"7","id":"rs573343884","clinical_significance":[]},{"seq_region_name":"7","id":"rs1172439328","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584290,"source":"dbSNP","strand":1,"feature_type":"variation","end":140584290,"alleles":["G","A"]},{"strand":1,"feature_type":"variation","end":140584291,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584291,"source":"dbSNP","seq_region_name":"7","id":"rs1798683137","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140584293,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584293,"clinical_significance":[],"id":"rs1260313947","seq_region_name":"7"},{"source":"dbSNP","start":140584295,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140584295,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798683367"},{"seq_region_name":"7","id":"rs1798683470","clinical_significance":[],"end":140584296,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140584296,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584296,"source":"dbSNP","strand":1,"feature_type":"variation","end":140584298,"alleles":["CTC","C"],"seq_region_name":"7","id":"rs1261925674","clinical_significance":[]},{"source":"dbSNP","start":140584298,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140584298,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1798684249","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140584304,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584304,"source":"dbSNP","seq_region_name":"7","id":"rs1798684365","clinical_significance":[]},{"seq_region_name":"7","id":"rs1315825669","clinical_significance":[],"end":140584308,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140584308,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140584309,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140584309,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs540622282","clinical_significance":[]},{"end":140584311,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140584311,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs559421273","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798684928","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584313,"feature_type":"variation","strand":1,"end":140584313,"alleles":["T","C"]},{"id":"rs1199615609","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584316,"source":"dbSNP","strand":1,"feature_type":"variation","end":140584316,"alleles":["C","T"]},{"strand":1,"feature_type":"variation","end":140584318,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584318,"source":"dbSNP","seq_region_name":"7","id":"rs1798685125","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584321,"feature_type":"variation","strand":1,"end":140584321,"alleles":["A","G"],"clinical_significance":[],"id":"rs113566280","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140584324,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584324,"source":"dbSNP","seq_region_name":"7","id":"rs1000843613","clinical_significance":[]},{"end":140584327,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140584327,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1798685349","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798685456","clinical_significance":[],"alleles":["A","G"],"end":140584329,"strand":1,"feature_type":"variation","start":140584329,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1032290324","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584330,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140584330},{"source":"dbSNP","start":140584331,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140584331,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1317356824","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584335,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140584335,"seq_region_name":"7","id":"rs1798685801","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140584336,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584336,"source":"dbSNP","seq_region_name":"7","id":"rs879753204","clinical_significance":[]},{"source":"dbSNP","start":140584342,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140584342,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798686031"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584349,"source":"dbSNP","strand":1,"feature_type":"variation","end":140584349,"alleles":["A","G"],"seq_region_name":"7","id":"rs1293920167","clinical_significance":[]},{"seq_region_name":"7","id":"rs1484213574","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584351,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140584351},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140584352,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584352,"source":"dbSNP","seq_region_name":"7","id":"rs1798686346","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798686450","clinical_significance":[],"start":140584357,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140584357,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs551308562","feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140584361,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584361},{"clinical_significance":[],"seq_region_name":"7","id":"rs890921434","source":"dbSNP","start":140584364,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140584364,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1798686876","clinical_significance":[],"start":140584367,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140584367,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"id":"rs943769722","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140584369,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584369,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140584372,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584372,"source":"dbSNP","seq_region_name":"7","id":"rs1798687223","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563158528","source":"dbSNP","start":140584381,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140584381,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584382,"source":"dbSNP","strand":1,"feature_type":"variation","end":140584382,"alleles":["G","A"],"seq_region_name":"7","id":"rs189263478","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140584383,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584383,"source":"dbSNP","id":"rs1798687556","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584385,"source":"dbSNP","strand":1,"feature_type":"variation","end":140584385,"alleles":["C","T"],"id":"rs1256169721","seq_region_name":"7","clinical_significance":[]},{"end":140584388,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140584388,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130642222"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584390,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140584390,"seq_region_name":"7","id":"rs1798687905","clinical_significance":[]},{"id":"rs2130642237","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["TTT","TT"],"end":140584394,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584392,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1798688024","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584396,"feature_type":"variation","strand":1,"end":140584396,"alleles":["C","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584398,"source":"dbSNP","strand":1,"feature_type":"variation","end":140584398,"alleles":["C","A","T"],"seq_region_name":"7","id":"rs758550704","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130642265","feature_type":"variation","strand":1,"end":140584399,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584399},{"start":140584408,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140584408,"strand":1,"feature_type":"variation","id":"rs1402958751","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140584411,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584411,"clinical_significance":[],"seq_region_name":"7","id":"rs1798688301"},{"alleles":["G","C"],"end":140584417,"strand":1,"feature_type":"variation","start":140584417,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs530914783","clinical_significance":[]},{"start":140584418,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140584418,"alleles":["T","G"],"strand":1,"feature_type":"variation","id":"rs1798688530","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584420,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140584420,"seq_region_name":"7","id":"rs1032695783","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140584421,"alleles":["G","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584421,"clinical_significance":[],"seq_region_name":"7","id":"rs892369742"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1170226708","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584423,"feature_type":"variation","strand":1,"end":140584423,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798689076","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140584428,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584428},{"start":140584433,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","T"],"end":140584433,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798689241","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140584435,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584435,"clinical_significance":[],"seq_region_name":"7","id":"rs1366621145"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1186798907","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584439,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140584439},{"id":"rs1798689836","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140584440,"strand":1,"feature_type":"variation","start":140584440,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["AGAG","AG"],"end":140584444,"feature_type":"variation","strand":1,"source":"dbSNP","start":140584441,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1360199204"},{"seq_region_name":"7","id":"rs1798690264","clinical_significance":[],"end":140584442,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140584442,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1798690443","clinical_significance":[],"end":140584446,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140584446,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1239835758","seq_region_name":"7","clinical_significance":[],"start":140584451,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140584451,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs952923432","clinical_significance":[],"alleles":["G","T"],"end":140584453,"strand":1,"feature_type":"variation","start":140584453,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1010227445","clinical_significance":[],"start":140584457,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C"],"end":140584457,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs984485696","clinical_significance":[],"end":140584458,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140584458,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["C","T"],"end":140584459,"feature_type":"variation","strand":1,"source":"dbSNP","start":140584459,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs908872421"},{"clinical_significance":[],"id":"rs1311632694","seq_region_name":"7","alleles":["T","C"],"end":140584462,"feature_type":"variation","strand":1,"source":"dbSNP","start":140584462,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140584465,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140584465,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs549537430"},{"end":140584466,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140584466,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs972230080","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130642408","end":140584470,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140584470,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs2130642418","clinical_significance":[],"start":140584471,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140584471,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1020239154","clinical_significance":[],"alleles":["G","A"],"end":140584472,"strand":1,"feature_type":"variation","start":140584472,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140584473,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140584473,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs2130642436","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1379558879","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584474,"feature_type":"variation","strand":1,"end":140584474,"alleles":["G","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1307457284","source":"dbSNP","start":140584477,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140584477,"alleles":["T","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798691942","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140584483,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584483},{"seq_region_name":"7","id":"rs1798692054","clinical_significance":[],"end":140584484,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140584484,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584485,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140584485,"seq_region_name":"7","id":"rs369454569","clinical_significance":[]},{"seq_region_name":"7","id":"rs971337854","clinical_significance":[],"end":140584490,"alleles":["T","A","G"],"strand":1,"feature_type":"variation","start":140584490,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs780032398","seq_region_name":"7","clinical_significance":[],"alleles":["T","A"],"end":140584492,"strand":1,"feature_type":"variation","start":140584492,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140584494,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584494,"source":"dbSNP","id":"rs1034416354","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140584496,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584496,"source":"dbSNP","seq_region_name":"7","id":"rs1798692622","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585690598","clinical_significance":[],"start":140584502,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140584502,"alleles":["T","G"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140584503,"alleles":["A","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584503,"clinical_significance":[],"id":"rs1798692985","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584504,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140584504,"clinical_significance":[],"id":"rs923014212","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1798693373","clinical_significance":[],"start":140584505,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140584505,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs933166241","alleles":["G","A"],"end":140584507,"feature_type":"variation","strand":1,"source":"dbSNP","start":140584507,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs959152545","clinical_significance":[],"start":140584511,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140584511,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"id":"rs1798693946","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584513,"source":"dbSNP","strand":1,"feature_type":"variation","end":140584513,"alleles":["G","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1388032811","source":"dbSNP","start":140584514,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140584514,"alleles":["G","A"],"feature_type":"variation","strand":1},{"id":"rs974256592","seq_region_name":"7","clinical_significance":[],"start":140584516,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140584516,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1798694464","clinical_significance":[],"strand":1,"feature_type":"variation","end":140584521,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584521,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1162570782","clinical_significance":[],"strand":1,"feature_type":"variation","end":140584523,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584523,"source":"dbSNP"},{"source":"dbSNP","start":140584525,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140584525,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1050197803"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140584527,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584527,"source":"dbSNP","seq_region_name":"7","id":"rs1757076127","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798695046","source":"dbSNP","start":140584537,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140584537,"alleles":["G","A"],"feature_type":"variation","strand":1},{"alleles":["C","T"],"end":140584538,"strand":1,"feature_type":"variation","start":140584538,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs889059070","clinical_significance":[]},{"seq_region_name":"7","id":"rs920210420","clinical_significance":[],"strand":1,"feature_type":"variation","end":140584542,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584542,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584546,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140584546,"clinical_significance":[],"seq_region_name":"7","id":"rs936583158"},{"id":"rs1798695871","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140584549,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584549,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584553,"feature_type":"variation","strand":1,"end":140584553,"alleles":["A","G"],"clinical_significance":[],"id":"rs1798696056","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140584554,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584554,"clinical_significance":[],"seq_region_name":"7","id":"rs1798696221"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1360144294","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584560,"feature_type":"variation","strand":1,"end":140584560,"alleles":["G","C"]},{"alleles":["A","T"],"end":140584561,"strand":1,"feature_type":"variation","start":140584561,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1213732556","clinical_significance":[]},{"start":140584562,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140584562,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585690712","clinical_significance":[]},{"seq_region_name":"7","id":"rs930211003","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584564,"source":"dbSNP","strand":1,"feature_type":"variation","end":140584564,"alleles":["T","G"]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140584568,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584568,"source":"dbSNP","seq_region_name":"7","id":"rs1224112613","clinical_significance":[]},{"alleles":["A","G"],"end":140584569,"strand":1,"feature_type":"variation","start":140584569,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs567756917","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs547217201","alleles":["T","C"],"end":140584570,"feature_type":"variation","strand":1,"source":"dbSNP","start":140584570,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","T"],"end":140584571,"feature_type":"variation","strand":1,"source":"dbSNP","start":140584571,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798697919"},{"clinical_significance":[],"seq_region_name":"7","id":"rs535044509","end":140584577,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140584577,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140584579,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140584579,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1205808808","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140584584,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584584,"source":"dbSNP","id":"rs2130642663","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140584587,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140584587,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1356390133"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584594,"feature_type":"variation","strand":1,"end":140584594,"alleles":["C","G"],"clinical_significance":[],"id":"rs1798698810","seq_region_name":"7"},{"source":"dbSNP","start":140584595,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140584595,"alleles":["T","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798698944"},{"source":"dbSNP","start":140584596,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140584596,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1207898126","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1798699200","seq_region_name":"7","alleles":["T","A","C"],"end":140584597,"feature_type":"variation","strand":1,"source":"dbSNP","start":140584597,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1798699348","clinical_significance":[],"alleles":["C","T"],"end":140584601,"strand":1,"feature_type":"variation","start":140584601,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["T","A"],"end":140584603,"feature_type":"variation","strand":1,"source":"dbSNP","start":140584603,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798699459"},{"start":140584605,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140584605,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1345176740","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1009536809","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140584610,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584610},{"clinical_significance":[],"seq_region_name":"7","id":"rs1279590892","feature_type":"variation","strand":1,"end":140584612,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584612},{"feature_type":"variation","strand":1,"end":140584615,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584615,"clinical_significance":[],"id":"rs1798699951","seq_region_name":"7"},{"alleles":["C","G"],"end":140584617,"strand":1,"feature_type":"variation","start":140584617,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1798700114","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584619,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140584619,"id":"rs982995113","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","C"],"end":140584626,"strand":1,"feature_type":"variation","start":140584626,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs912237352","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584632,"feature_type":"variation","strand":1,"end":140584632,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1798700498"},{"end":140584636,"alleles":["A","G","T"],"strand":1,"feature_type":"variation","start":140584636,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs943686917","clinical_significance":[]},{"clinical_significance":[],"id":"rs2130642794","seq_region_name":"7","end":140584637,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140584637,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["G","A"],"end":140584641,"feature_type":"variation","strand":1,"source":"dbSNP","start":140584641,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1275070014"},{"end":140584642,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140584642,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1260538178"},{"seq_region_name":"7","id":"rs1798701048","clinical_significance":[],"start":140584644,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140584644,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798701162","source":"dbSNP","start":140584645,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140584645,"alleles":["A","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1438238966","feature_type":"variation","strand":1,"end":140584646,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584646},{"seq_region_name":"7","id":"rs1585690916","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["AAGAAG","AAG"],"end":140584651,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584646,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140584651,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584651,"source":"dbSNP","seq_region_name":"7","id":"rs1002844386","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798701710","clinical_significance":[],"strand":1,"feature_type":"variation","end":140584652,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584652,"source":"dbSNP"},{"source":"dbSNP","start":140584653,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140584653,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585690941"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1039876021","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584657,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140584657},{"seq_region_name":"7","id":"rs1033943455","clinical_significance":[],"start":140584658,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","T"],"end":140584658,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798702258","feature_type":"variation","strand":1,"end":140584662,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584662},{"source":"dbSNP","start":140584663,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140584663,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs952820499"},{"start":140584665,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140584665,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1191457704","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584668,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140584668,"seq_region_name":"7","id":"rs1798702628","clinical_significance":[]},{"clinical_significance":[],"id":"rs1798702757","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584669,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140584669},{"seq_region_name":"7","id":"rs2130642904","clinical_significance":[],"alleles":["C","T"],"end":140584670,"strand":1,"feature_type":"variation","start":140584670,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140584674,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140584674,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs899560455","clinical_significance":[]},{"seq_region_name":"7","id":"rs1005723783","clinical_significance":[],"start":140584677,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140584677,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs936529501","alleles":["T","A"],"end":140584680,"feature_type":"variation","strand":1,"source":"dbSNP","start":140584680,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1015807168","seq_region_name":"7","clinical_significance":[],"end":140584683,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140584683,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs767205593","alleles":["G","A"],"end":140584703,"feature_type":"variation","strand":1,"source":"dbSNP","start":140584703,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140584704,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140584704,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs962090592","clinical_significance":[]},{"seq_region_name":"7","id":"rs750440609","clinical_significance":[],"strand":1,"feature_type":"variation","end":140584710,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584710,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1193124777","end":140584713,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140584713,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584714,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140584714,"id":"rs1798704092","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798704262","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584715,"feature_type":"variation","strand":1,"end":140584715,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1477130455","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584716,"feature_type":"variation","strand":1,"end":140584716,"alleles":["C","T"]},{"clinical_significance":[],"id":"rs1435344919","seq_region_name":"7","source":"dbSNP","start":140584717,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140584717,"alleles":["A","G"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140584720,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584720,"clinical_significance":[],"id":"rs1246352709","seq_region_name":"7"},{"source":"dbSNP","start":140584723,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140584723,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1194429149"},{"feature_type":"variation","strand":1,"end":140584727,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584727,"clinical_significance":[],"seq_region_name":"7","id":"rs1489339614"},{"seq_region_name":"7","id":"rs1798705471","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584729,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140584729},{"clinical_significance":[],"id":"rs141808347","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584730,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140584730},{"clinical_significance":[],"seq_region_name":"7","id":"rs571864775","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140584731,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584731},{"strand":1,"feature_type":"variation","alleles":["CACA","CA"],"end":140584735,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584732,"source":"dbSNP","seq_region_name":"7","id":"rs1349030664","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1420317669","alleles":["A","G"],"end":140584733,"feature_type":"variation","strand":1,"source":"dbSNP","start":140584733,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["AGAGA","AGA"],"end":140584739,"strand":1,"feature_type":"variation","start":140584735,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1281093436","clinical_significance":[]},{"id":"rs892421789","seq_region_name":"7","clinical_significance":[],"end":140584739,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140584739,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140584740,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TTTTTTTTT","TTTTTTTT","TTTTTTTTTT"],"end":140584748,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs954417729","clinical_significance":[]},{"source":"dbSNP","start":140584746,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140584746,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798706591"},{"end":140584749,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140584749,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs760497736","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs181161540","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140584758,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584758},{"seq_region_name":"7","id":"rs1798707162","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584759,"source":"dbSNP","strand":1,"feature_type":"variation","end":140584759,"alleles":["A","G"]},{"id":"rs150192078","seq_region_name":"7","clinical_significance":[],"end":140584760,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140584760,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1400059715","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584762,"feature_type":"variation","strand":1,"end":140584762,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1341882906","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140584770,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584770,"source":"dbSNP"},{"alleles":["G","A"],"end":140584771,"feature_type":"variation","strand":1,"source":"dbSNP","start":140584771,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1046271074"},{"alleles":["A","G"],"end":140584774,"feature_type":"variation","strand":1,"source":"dbSNP","start":140584774,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1399391703"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584777,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140584777,"seq_region_name":"7","id":"rs1798707848","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584779,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140584779,"seq_region_name":"7","id":"rs910472887","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584779,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TACACATACA","TACA"],"end":140584788,"seq_region_name":"7","id":"rs1798708071","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1177887708","feature_type":"variation","strand":1,"alleles":["A","ATGTGTAAGTTTA"],"end":140584782,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584782},{"clinical_significance":[],"seq_region_name":"7","id":"rs1412578030","alleles":["C","T"],"end":140584783,"feature_type":"variation","strand":1,"source":"dbSNP","start":140584783,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1798708423","clinical_significance":[],"alleles":["T","C"],"end":140584785,"strand":1,"feature_type":"variation","start":140584785,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1424697005","seq_region_name":"7","clinical_significance":[],"start":140584787,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140584787,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"start":140584788,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140584788,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1171704714","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140584791,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584791,"source":"dbSNP","seq_region_name":"7","id":"rs1798708761","clinical_significance":[]},{"end":140584792,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140584792,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1478840761"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140584793,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584793,"source":"dbSNP","seq_region_name":"7","id":"rs936632005","clinical_significance":[]},{"start":140584794,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140584794,"alleles":["A","ATTTGTAA"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1193052537","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798709225","source":"dbSNP","start":140584794,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AA","AAA"],"end":140584795,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs2130643176","clinical_significance":[],"start":140584796,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140584796,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1798709333","seq_region_name":"7","end":140584797,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140584797,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1798709443","clinical_significance":[],"alleles":["T","G"],"end":140584798,"strand":1,"feature_type":"variation","start":140584798,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140584802,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140584802,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1430251949"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140584803,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584803,"source":"dbSNP","seq_region_name":"7","id":"rs1239752012","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584804,"source":"dbSNP","strand":1,"feature_type":"variation","end":140584804,"alleles":["A","G"],"seq_region_name":"7","id":"rs1798709765","clinical_significance":[]},{"id":"rs1798709887","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584807,"source":"dbSNP","strand":1,"feature_type":"variation","end":140584807,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs907230952","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584808,"source":"dbSNP","strand":1,"feature_type":"variation","end":140584808,"alleles":["G","A"]},{"clinical_significance":[],"id":"rs1798710123","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584809,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140584809},{"end":140584814,"alleles":["TT","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140584813,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1208394469"},{"strand":1,"feature_type":"variation","end":140584815,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584815,"source":"dbSNP","seq_region_name":"7","id":"rs1275708304","clinical_significance":[]},{"seq_region_name":"7","id":"rs1262092082","clinical_significance":[],"start":140584822,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140584822,"strand":1,"feature_type":"variation"},{"start":140584827,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140584827,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130643255","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140584828,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584828,"source":"dbSNP","seq_region_name":"7","id":"rs1798710578","clinical_significance":[]},{"alleles":["A","G","T"],"end":140584830,"strand":1,"feature_type":"variation","start":140584830,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1053542435","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140584836,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584836,"clinical_significance":[],"seq_region_name":"7","id":"rs1002858407"},{"seq_region_name":"7","id":"rs1034877852","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584837,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140584837},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585691392","source":"dbSNP","start":140584838,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140584838,"alleles":["G","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1302500569","clinical_significance":[],"alleles":["T","C"],"end":140584839,"strand":1,"feature_type":"variation","start":140584839,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs557278304","source":"dbSNP","start":140584849,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140584849,"alleles":["T","A","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs943825367","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584850,"feature_type":"variation","strand":1,"end":140584850,"alleles":["A","T"]},{"seq_region_name":"7","id":"rs906496791","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584850,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AAAAAAA","AAAAAA","AAAAAAAA"],"end":140584856},{"seq_region_name":"7","id":"rs1798711804","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140584856,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584856,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1798711911","clinical_significance":[],"alleles":["C","A"],"end":140584858,"strand":1,"feature_type":"variation","start":140584858,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1467324541","source":"dbSNP","start":140584859,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140584859,"alleles":["C","A","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs996119698","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584860,"source":"dbSNP","strand":1,"feature_type":"variation","end":140584860,"alleles":["A","C"]},{"clinical_significance":[],"id":"rs1798712291","seq_region_name":"7","feature_type":"variation","strand":1,"end":140584861,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584861},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584862,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140584862,"seq_region_name":"7","id":"rs1218104366","clinical_significance":[]},{"start":140584862,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140584866,"alleles":["ATATA","ATA"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1170003604","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584865,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140584865,"clinical_significance":[],"seq_region_name":"7","id":"rs1424494343"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798712752","source":"dbSNP","start":140584866,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140584866,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140584867,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140584867,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs765348486"},{"id":"rs1180667865","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140584869,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584869,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1472674287","feature_type":"variation","strand":1,"end":140584871,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584871},{"seq_region_name":"7","id":"rs1239235168","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140584872,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584872,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140584874,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584874,"clinical_significance":[],"seq_region_name":"7","id":"rs1445953543"},{"source":"dbSNP","start":140584875,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140584875,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs756136139"},{"end":140584876,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140584876,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs575754677","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140584880,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584880,"source":"dbSNP","id":"rs1015754725","seq_region_name":"7","clinical_significance":[]},{"end":140584887,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140584887,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798713852"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130643462","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584888,"feature_type":"variation","strand":1,"end":140584888,"alleles":["A","G"]},{"end":140584889,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140584889,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798713964"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798714085","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584890,"feature_type":"variation","strand":1,"end":140584890,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1226592953","alleles":["A","G"],"end":140584892,"feature_type":"variation","strand":1,"source":"dbSNP","start":140584892,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs961587840","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584893,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140584893},{"source":"dbSNP","start":140584897,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","-"],"end":140584897,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1798714424","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1309623401","clinical_significance":[],"start":140584898,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140584898,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs993626331","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584910,"source":"dbSNP","strand":1,"feature_type":"variation","end":140584910,"alleles":["A","G"]},{"strand":1,"feature_type":"variation","end":140584911,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584911,"source":"dbSNP","seq_region_name":"7","id":"rs1398314092","clinical_significance":[]},{"start":140584911,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["CCC","CC"],"end":140584913,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798715413","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140584915,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584915,"clinical_significance":[],"seq_region_name":"7","id":"rs1798715532"},{"end":140584916,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140584916,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1192156528","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584918,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140584918,"clinical_significance":[],"seq_region_name":"7","id":"rs1798715764"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140584919,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584919,"source":"dbSNP","seq_region_name":"7","id":"rs1394970034","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140584921,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584921,"clinical_significance":[],"seq_region_name":"7","id":"rs1798716003"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1458448890","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584926,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140584926},{"feature_type":"variation","strand":1,"end":140584927,"alleles":["G","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584927,"clinical_significance":[],"seq_region_name":"7","id":"rs373496561"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798716377","end":140584932,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140584932,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1798716497","clinical_significance":[],"strand":1,"feature_type":"variation","end":140584936,"alleles":["T","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584936,"source":"dbSNP"},{"source":"dbSNP","start":140584938,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140584938,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1163282989"},{"seq_region_name":"7","id":"rs1423686886","clinical_significance":[],"strand":1,"feature_type":"variation","end":140584939,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584939,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140584942,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584942,"clinical_significance":[],"seq_region_name":"7","id":"rs1798716902"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798717016","source":"dbSNP","start":140584945,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140584945,"feature_type":"variation","strand":1},{"alleles":["C","T"],"end":140584948,"feature_type":"variation","strand":1,"source":"dbSNP","start":140584948,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1381479151"},{"seq_region_name":"7","id":"rs1798717244","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584950,"source":"dbSNP","strand":1,"feature_type":"variation","end":140584950,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1180858458","clinical_significance":[],"end":140584951,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140584951,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs536439976","seq_region_name":"7","clinical_significance":[],"end":140584953,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140584953,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798717664","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140584955,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584955},{"source":"dbSNP","start":140584957,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140584957,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1161026549"},{"start":140584961,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140584961,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1405849021","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584964,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140584964,"seq_region_name":"7","id":"rs951490003","clinical_significance":[]},{"source":"dbSNP","start":140584965,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140584965,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs983042598","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140584967,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584967,"clinical_significance":[],"id":"rs1488513440","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1324379926","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140584972,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584972},{"seq_region_name":"7","id":"rs1798718858","clinical_significance":[],"end":140584978,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140584978,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs912794298","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140584985,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140584985,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1218747962","source":"dbSNP","start":140584987,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140584987,"alleles":["C","A"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140584988,"feature_type":"variation","strand":1,"end":140584988,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130643656"},{"end":140584991,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140584991,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs555091862"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1358588740","source":"dbSNP","start":140585001,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140585001,"feature_type":"variation","strand":1},{"id":"rs1286674351","seq_region_name":"7","clinical_significance":[],"start":140585005,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140585005,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585006,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140585006,"seq_region_name":"7","id":"rs1242017691","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs573384454","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585007,"feature_type":"variation","strand":1,"end":140585007,"alleles":["T","C","G"]},{"seq_region_name":"7","id":"rs1798719852","clinical_significance":[],"start":140585009,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140585009,"strand":1,"feature_type":"variation"},{"id":"rs1798719972","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140585012,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585012,"source":"dbSNP"},{"source":"dbSNP","start":140585014,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140585014,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs910251798"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798720263","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585016,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140585016},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798720386","source":"dbSNP","start":140585018,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["GTGAAACCCCGT","GT"],"end":140585029,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1798720507","clinical_significance":[],"alleles":["C","T"],"end":140585027,"strand":1,"feature_type":"variation","start":140585027,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140585028,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140585028,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs529601007","clinical_significance":[]},{"clinical_significance":[],"id":"rs1798720738","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585030,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140585030},{"start":140585032,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140585032,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs377557965","clinical_significance":[]},{"id":"rs2062317","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585034,"source":"dbSNP","strand":1,"feature_type":"variation","end":140585034,"alleles":["A","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1277769790","source":"dbSNP","start":140585036,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140585036,"alleles":["A","T"],"feature_type":"variation","strand":1},{"id":"rs781179408","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140585041,"alleles":["AAAAAA","AAAAAAA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585036,"source":"dbSNP"},{"id":"rs936430683","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140585056,"strand":1,"feature_type":"variation","start":140585056,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140585062,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140585062,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798721499","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1361680720","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585063,"feature_type":"variation","strand":1,"end":140585063,"alleles":["T","C"]},{"alleles":["G","A"],"end":140585065,"feature_type":"variation","strand":1,"source":"dbSNP","start":140585065,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798721741"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1161028040","feature_type":"variation","strand":1,"end":140585066,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585066},{"clinical_significance":[],"id":"rs545248127","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140585067,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585067},{"clinical_significance":[],"seq_region_name":"7","id":"rs1380136406","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585067,"feature_type":"variation","strand":1,"end":140585071,"alleles":["GTGTG","GTG"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1433342786","end":140585068,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140585068,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1798722359","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585076,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140585076},{"source":"dbSNP","start":140585079,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140585079,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798722475"},{"clinical_significance":[],"seq_region_name":"7","id":"rs374526731","source":"dbSNP","start":140585081,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140585081,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140585082,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585082,"source":"dbSNP","seq_region_name":"7","id":"rs1291502319","clinical_significance":[]},{"source":"dbSNP","start":140585083,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140585083,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs563425569"},{"source":"dbSNP","start":140585097,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140585097,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1188895097"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1466885943","source":"dbSNP","start":140585098,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140585098,"alleles":["T","A","C","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs2130643871","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585101,"source":"dbSNP","strand":1,"feature_type":"variation","end":140585101,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563159064","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140585103,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585103},{"source":"dbSNP","start":140585104,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140585104,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1212161906"},{"seq_region_name":"7","id":"rs1263773370","clinical_significance":[],"start":140585104,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140585106,"alleles":["GGG","GG"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140585107,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585107,"clinical_significance":[],"seq_region_name":"7","id":"rs1563159072"},{"feature_type":"variation","strand":1,"end":140585108,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585108,"clinical_significance":[],"seq_region_name":"7","id":"rs530771631"},{"end":140585111,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140585111,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1218791416","clinical_significance":[]},{"start":140585119,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140585119,"strand":1,"feature_type":"variation","id":"rs1563159078","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140585125,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585125,"source":"dbSNP","id":"rs1351218652","seq_region_name":"7","clinical_significance":[]},{"end":140585128,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140585128,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798724260","clinical_significance":[]},{"seq_region_name":"7","id":"rs1252737591","clinical_significance":[],"strand":1,"feature_type":"variation","end":140585131,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585131,"source":"dbSNP"},{"alleles":["A","G","T"],"end":140585132,"strand":1,"feature_type":"variation","start":140585132,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798724515","clinical_significance":[]},{"id":"rs1233715996","seq_region_name":"7","clinical_significance":[],"alleles":["TGCGCCGTGATTGC","TGC"],"end":140585154,"strand":1,"feature_type":"variation","start":140585141,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140585143,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140585143,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs913751010"},{"id":"rs945188145","seq_region_name":"7","clinical_significance":[],"start":140585144,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140585144,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"id":"rs1046323023","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140585147,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585147,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1469630000","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585149,"feature_type":"variation","strand":1,"end":140585149,"alleles":["G","C"]},{"source":"dbSNP","start":140585151,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140585151,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs938114380"},{"seq_region_name":"7","id":"rs1055119201","clinical_significance":[],"start":140585153,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C"],"end":140585153,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798725532","source":"dbSNP","start":140585160,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140585160,"alleles":["T","C"],"feature_type":"variation","strand":1},{"end":140585164,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140585164,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130643999","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798725628","feature_type":"variation","strand":1,"end":140585167,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585167},{"clinical_significance":[],"seq_region_name":"7","id":"rs1360453690","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585169,"feature_type":"variation","strand":1,"end":140585169,"alleles":["G","C"]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140585171,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585171,"clinical_significance":[],"seq_region_name":"7","id":"rs1798725855"},{"seq_region_name":"7","id":"rs1798725957","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140585172,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585172,"source":"dbSNP"},{"source":"dbSNP","start":140585175,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140585175,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1173483188"},{"seq_region_name":"7","id":"rs549176578","clinical_significance":[],"end":140585176,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140585176,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs906437435","seq_region_name":"7","clinical_significance":[],"start":140585179,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140585179,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585181,"source":"dbSNP","strand":1,"feature_type":"variation","end":140585181,"alleles":["G","C"],"id":"rs1003321364","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140585184,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585184,"clinical_significance":[],"id":"rs752796841","seq_region_name":"7"},{"seq_region_name":"7","id":"rs561403050","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140585185,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585185,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1237379540","clinical_significance":[],"strand":1,"feature_type":"variation","end":140585187,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585187,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1173566482","feature_type":"variation","strand":1,"alleles":["AA","A"],"end":140585189,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585188},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585192,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140585192,"seq_region_name":"7","id":"rs995615144","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1164525479","feature_type":"variation","strand":1,"end":140585193,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585193},{"end":140585195,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140585195,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798727136","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130644114","feature_type":"variation","strand":1,"end":140585197,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585197},{"clinical_significance":[],"id":"rs1798727259","seq_region_name":"7","alleles":["A","G"],"end":140585201,"feature_type":"variation","strand":1,"source":"dbSNP","start":140585201,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1027040473","seq_region_name":"7","feature_type":"variation","strand":1,"end":140585202,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585202},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140585209,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585209,"clinical_significance":[],"seq_region_name":"7","id":"rs1798727494"},{"end":140585221,"alleles":["CAACAACAACAAC","CAACAACAAC","CAACAACAACAACAAC"],"strand":1,"feature_type":"variation","start":140585209,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs569871863","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140585210,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585210,"source":"dbSNP","seq_region_name":"7","id":"rs897283002","clinical_significance":[]},{"id":"rs1484141508","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140585212,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585212,"source":"dbSNP"},{"seq_region_name":"7","id":"rs149372958","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585215,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","G","T"],"end":140585215},{"clinical_significance":[],"seq_region_name":"7","id":"rs1318890427","source":"dbSNP","start":140585216,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140585216,"alleles":["A","G"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585217,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140585217,"clinical_significance":[],"id":"rs1280099676","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798728418","alleles":["A","C"],"end":140585219,"feature_type":"variation","strand":1,"source":"dbSNP","start":140585219,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585220,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140585220,"id":"rs1216909312","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1030282697","alleles":["C","A","T"],"end":140585221,"feature_type":"variation","strand":1,"source":"dbSNP","start":140585221,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1398119798","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585222,"feature_type":"variation","strand":1,"alleles":["C","A","G"],"end":140585222},{"seq_region_name":"7","id":"rs1798729022","clinical_significance":[],"strand":1,"feature_type":"variation","end":140585227,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585227,"source":"dbSNP"},{"alleles":["G","A"],"end":140585230,"feature_type":"variation","strand":1,"source":"dbSNP","start":140585230,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798729118"},{"clinical_significance":[],"id":"rs1335106232","seq_region_name":"7","alleles":["AAAA","AA"],"end":140585236,"feature_type":"variation","strand":1,"source":"dbSNP","start":140585233,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585239,"feature_type":"variation","strand":1,"end":140585239,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1448079310"},{"seq_region_name":"7","id":"rs1004364876","clinical_significance":[],"start":140585248,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140585248,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585249,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140585249,"clinical_significance":[],"id":"rs1334273065","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140585251,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585251,"source":"dbSNP","seq_region_name":"7","id":"rs115527264","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798729851","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585258,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140585258},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585260,"source":"dbSNP","strand":1,"feature_type":"variation","end":140585260,"alleles":["T","A"],"seq_region_name":"7","id":"rs1332095988","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798730089","clinical_significance":[],"end":140585264,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140585264,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798730227","source":"dbSNP","start":140585265,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140585265,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140585266,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140585266,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1232269626"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798730464","end":140585267,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140585267,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140585271,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585271,"clinical_significance":[],"seq_region_name":"7","id":"rs1258384205"},{"seq_region_name":"7","id":"rs1319021604","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585272,"source":"dbSNP","strand":1,"feature_type":"variation","end":140585272,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130644290","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140585278,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585278},{"alleles":["A","G"],"end":140585279,"feature_type":"variation","strand":1,"source":"dbSNP","start":140585279,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1476568104"},{"seq_region_name":"7","id":"rs2130644312","clinical_significance":[],"end":140585287,"alleles":["AGAG","AG"],"strand":1,"feature_type":"variation","start":140585284,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140585285,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140585285,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1197928756","seq_region_name":"7"},{"seq_region_name":"7","id":"rs2130644331","clinical_significance":[],"start":140585287,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140585287,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1188213207","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140585288,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585288,"source":"dbSNP"},{"id":"rs146321382","seq_region_name":"7","clinical_significance":[],"end":140585289,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140585289,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs2130644362","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585289,"source":"dbSNP","strand":1,"feature_type":"variation","end":140585289,"alleles":["A","-"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585296,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140585296,"seq_region_name":"7","id":"rs1253745910","clinical_significance":[]},{"end":140585297,"alleles":["T","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140585297,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs758428734"},{"start":140585309,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G","T"],"end":140585309,"strand":1,"feature_type":"variation","id":"rs1458352326","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1260261636","clinical_significance":[],"end":140585314,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140585314,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs920942376","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140585316,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585316,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140585318,"alleles":["TT","TTT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585317,"clinical_significance":[],"seq_region_name":"7","id":"rs1196798861"},{"seq_region_name":"7","id":"rs1798732183","clinical_significance":[],"end":140585318,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140585318,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1188910376","seq_region_name":"7","clinical_significance":[],"start":140585319,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140585319,"strand":1,"feature_type":"variation"},{"start":140585321,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140585321,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs957907812","clinical_significance":[]},{"seq_region_name":"7","id":"rs989209383","clinical_significance":[],"end":140585322,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","start":140585322,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585325,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140585325,"clinical_significance":[],"seq_region_name":"7","id":"rs1247696526"},{"clinical_significance":[],"seq_region_name":"7","id":"rs778663885","alleles":["C","G","T"],"end":140585327,"feature_type":"variation","strand":1,"source":"dbSNP","start":140585327,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1474303514","seq_region_name":"7","source":"dbSNP","start":140585328,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140585328,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140585332,"alleles":["G","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585332,"clinical_significance":[],"seq_region_name":"7","id":"rs550946916"},{"end":140585335,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140585335,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1448029192"},{"seq_region_name":"7","id":"rs1798733240","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585344,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140585344},{"start":140585346,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140585346,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585692668","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1333011281","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585352,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140585352},{"start":140585353,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140585353,"alleles":["G","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798733572","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140585362,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585362,"clinical_significance":[],"seq_region_name":"7","id":"rs1798733675"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140585363,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585363,"source":"dbSNP","seq_region_name":"7","id":"rs1798733793","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1407683357","feature_type":"variation","strand":1,"end":140585368,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585368},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798734048","end":140585375,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140585375,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140585381,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G","T"],"end":140585381,"strand":1,"feature_type":"variation","id":"rs913636394","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","G"],"end":140585382,"feature_type":"variation","strand":1,"source":"dbSNP","start":140585382,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs147141254","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1459317170","seq_region_name":"7","feature_type":"variation","strand":1,"end":140585384,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585384},{"seq_region_name":"7","id":"rs1798734528","clinical_significance":[],"end":140585385,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140585385,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585386,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140585386,"id":"rs1046209209","seq_region_name":"7","clinical_significance":[]},{"start":140585398,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140585398,"alleles":["G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1182694526","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","CC"],"end":140585399,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585399,"clinical_significance":[],"seq_region_name":"7","id":"rs1798734882"},{"id":"rs927911567","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585403,"source":"dbSNP","strand":1,"feature_type":"variation","end":140585403,"alleles":["T","G"]},{"seq_region_name":"7","id":"rs966905786","clinical_significance":[],"start":140585404,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140585404,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"alleles":["GAGCAGAGGGG","-"],"end":140585416,"strand":1,"feature_type":"variation","start":140585406,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1554474212","clinical_significance":[]},{"seq_region_name":"7","id":"rs1177078405","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585411,"source":"dbSNP","strand":1,"feature_type":"variation","end":140585411,"alleles":["G","C"]},{"alleles":["G","A"],"end":140585413,"feature_type":"variation","strand":1,"source":"dbSNP","start":140585413,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1437299750","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1554474217","clinical_significance":[],"start":140585417,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140585416,"alleles":["-","TTTTTTTTTTT"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs73498495","seq_region_name":"7","end":140585424,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140585424,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1798735820","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585427,"source":"dbSNP","strand":1,"feature_type":"variation","end":140585427,"alleles":["A","T"]},{"seq_region_name":"7","id":"rs1055420765","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585431,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140585431},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585432,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140585432,"clinical_significance":[],"seq_region_name":"7","id":"rs1585692821"},{"clinical_significance":[],"id":"rs1798736332","seq_region_name":"7","feature_type":"variation","strand":1,"end":140585433,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585433},{"alleles":["G","C"],"end":140585434,"strand":1,"feature_type":"variation","start":140585434,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs79266599","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140585438,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585438,"clinical_significance":[],"seq_region_name":"7","id":"rs938061878"},{"strand":1,"feature_type":"variation","end":140585444,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585444,"source":"dbSNP","seq_region_name":"7","id":"rs1798736837","clinical_significance":[]},{"source":"dbSNP","start":140585451,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140585451,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1241304098"},{"seq_region_name":"7","id":"rs931275945","clinical_significance":[],"end":140585455,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140585455,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140585456,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140585456,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1452733334"},{"alleles":["T","C"],"end":140585460,"feature_type":"variation","strand":1,"source":"dbSNP","start":140585460,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1048532385"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140585461,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585461,"clinical_significance":[],"seq_region_name":"7","id":"rs1353020364"},{"clinical_significance":[],"seq_region_name":"7","id":"rs139634965","source":"dbSNP","start":140585476,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140585476,"feature_type":"variation","strand":1},{"end":140585477,"alleles":["G","A","C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140585477,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1004417424"},{"end":140585480,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140585480,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798737917","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140585482,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585482,"clinical_significance":[],"seq_region_name":"7","id":"rs1342022139"},{"start":140585483,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140585483,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs1585692938","seq_region_name":"7","clinical_significance":[]},{"id":"rs1363609836","seq_region_name":"7","clinical_significance":[],"end":140585487,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140585487,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1585692955","seq_region_name":"7","clinical_significance":[],"start":140585488,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140585488,"alleles":["T","G"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585491,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140585491,"seq_region_name":"7","id":"rs1019790632","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585692974","clinical_significance":[],"start":140585494,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140585494,"alleles":["T","G"],"strand":1,"feature_type":"variation"},{"id":"rs1382002222","seq_region_name":"7","clinical_significance":[],"start":140585496,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140585496,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585497,"feature_type":"variation","strand":1,"end":140585498,"alleles":["CC","CCC"],"clinical_significance":[],"seq_region_name":"7","id":"rs1420075401"},{"seq_region_name":"7","id":"rs1798738944","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140585498,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585498,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798739050","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140585499,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585499},{"start":140585506,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140585506,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1156606018","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140585509,"alleles":["G","A","C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585509,"source":"dbSNP","seq_region_name":"7","id":"rs901298166","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798739575","source":"dbSNP","start":140585516,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140585516,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1037651815","feature_type":"variation","strand":1,"end":140585517,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585517},{"start":140585518,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140585518,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs558117527","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798740143","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585520,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140585520},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140585522,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585522,"source":"dbSNP","id":"rs1798740317","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs756542978","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585523,"source":"dbSNP","strand":1,"feature_type":"variation","end":140585523,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563159297","end":140585524,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140585524,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["A","G"],"end":140585526,"feature_type":"variation","strand":1,"source":"dbSNP","start":140585526,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs934271592"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585528,"source":"dbSNP","strand":1,"feature_type":"variation","end":140585528,"alleles":["A","G"],"id":"rs1218075286","seq_region_name":"7","clinical_significance":[]},{"start":140585532,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140585532,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1051260135","clinical_significance":[]},{"seq_region_name":"7","id":"rs889975810","clinical_significance":[],"start":140585537,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140585537,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1798741594","clinical_significance":[],"start":140585538,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["GCCACCATGCTTTGGCCCCCTCTCCTGCCACCAT","GCCACCAT"],"end":140585571,"strand":1,"feature_type":"variation"},{"end":140585542,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140585542,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs746425005","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140585546,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585546,"clinical_significance":[],"id":"rs770093818","seq_region_name":"7"},{"start":140585547,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140585547,"alleles":["C","A"],"strand":1,"feature_type":"variation","id":"rs1389199403","seq_region_name":"7","clinical_significance":[]},{"end":140585548,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140585548,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1336624167"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585553,"source":"dbSNP","strand":1,"feature_type":"variation","end":140585553,"alleles":["C","A","T"],"seq_region_name":"7","id":"rs536478031","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585558,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140585558,"clinical_significance":[],"seq_region_name":"7","id":"rs1798742686"},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140585559,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585559,"clinical_significance":[],"id":"rs554707237","seq_region_name":"7"},{"start":140585561,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140585561,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs774491021","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140585562,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585562,"clinical_significance":[],"seq_region_name":"7","id":"rs761975899"},{"seq_region_name":"7","id":"rs767742397","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585567,"source":"dbSNP","strand":1,"feature_type":"variation","end":140585567,"alleles":["A","G"]},{"feature_type":"variation","strand":1,"end":140585571,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585571,"clinical_significance":[],"seq_region_name":"7","id":"rs1437949147"},{"id":"rs573421276","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585572,"source":"dbSNP","strand":1,"feature_type":"variation","end":140585572,"alleles":["T","A","C"]},{"strand":1,"feature_type":"variation","end":140585575,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585575,"source":"dbSNP","id":"rs1253031564","seq_region_name":"7","clinical_significance":[]},{"end":140585580,"alleles":["GGGG","GGG"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140585577,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs761424131"},{"clinical_significance":[],"seq_region_name":"7","id":"rs759579143","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585578,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140585578},{"seq_region_name":"7","id":"rs1798744377","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585579,"source":"dbSNP","strand":1,"feature_type":"variation","end":140585579,"alleles":["G","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585580,"feature_type":"variation","strand":1,"end":140585580,"alleles":["G","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs765059457"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140585582,"consequence_type":"splice_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585582,"clinical_significance":[],"id":"rs373546249","seq_region_name":"7"},{"start":140585583,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_donor_region_variant","end":140585583,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs377485057","clinical_significance":[]},{"end":140585584,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140585584,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_donor_5th_base_variant","id":"rs1182028838","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs989094823","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"splice_donor_region_variant","start":140585585,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140585585},{"alleles":["C","T"],"end":140585588,"feature_type":"variation","strand":1,"source":"dbSNP","start":140585588,"consequence_type":"splice_donor_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1007239590"},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140585590,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140585590,"seq_region_name":"7","id":"rs1798745582","clinical_significance":[]},{"end":140585593,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140585593,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs370908430","clinical_significance":[]},{"alleles":["T","C"],"end":140585598,"feature_type":"variation","strand":1,"source":"dbSNP","start":140585598,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130645036"},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585599,"feature_type":"variation","strand":1,"end":140585599,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs751214812"},{"id":"rs1315917604","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"inframe_deletion","start":140585599,"source":"dbSNP","strand":1,"feature_type":"variation","end":140585619,"alleles":["GTGTCAGGGATGGAAGAGGTG","GTG"]},{"seq_region_name":"7","id":"rs1172923912","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140585601,"source":"dbSNP","strand":1,"feature_type":"variation","end":140585601,"alleles":["G","A","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs756740174","source":"dbSNP","start":140585606,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140585606,"alleles":["G","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1461862174","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140585609,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585609},{"seq_region_name":"7","id":"rs1798747150","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140585610,"source":"dbSNP","strand":1,"feature_type":"variation","end":140585610,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1798747331","clinical_significance":[],"end":140585611,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140585611,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1173657980","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585612,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140585612},{"seq_region_name":"7","id":"rs1406235839","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140585616,"source":"dbSNP","strand":1,"feature_type":"variation","end":140585616,"alleles":["G","A","C"]},{"source":"dbSNP","start":140585617,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140585617,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs893437763"},{"source":"dbSNP","start":140585619,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140585619,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs780699896","seq_region_name":"7"},{"alleles":["G","A"],"end":140585620,"strand":1,"feature_type":"variation","start":140585620,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","id":"rs1798748210","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798748352","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585621,"feature_type":"variation","strand":1,"end":140585621,"alleles":["G","C"]},{"source":"dbSNP","start":140585625,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","end":140585625,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs769220604"},{"clinical_significance":[],"id":"rs201794849","seq_region_name":"7","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585629,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140585629},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140585631,"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140585631,"source":"dbSNP","seq_region_name":"7","id":"rs1798748627","clinical_significance":[]},{"clinical_significance":[],"id":"rs1798748756","seq_region_name":"7","source":"dbSNP","start":140585632,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140585632,"alleles":["A","G"],"feature_type":"variation","strand":1},{"alleles":["A","G","T"],"end":140585641,"strand":1,"feature_type":"variation","start":140585641,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs375591057","clinical_significance":[]},{"source":"dbSNP","start":140585641,"consequence_type":"frameshift_variant","assembly_name":"GRCh38","alleles":["ACACAC","ACAC"],"end":140585646,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1381529404"},{"id":"rs1020695552","seq_region_name":"7","clinical_significance":[],"start":140585644,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140585644,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"id":"rs1297374799","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140585645,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140585645},{"source":"dbSNP","start":140585646,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140585646,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs966642659"},{"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140585649,"source":"dbSNP","strand":1,"feature_type":"variation","end":140585649,"alleles":["C","T"],"id":"rs368228532","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs749650533","seq_region_name":"7","feature_type":"variation","strand":1,"end":140585650,"alleles":["T","C"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585650},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798749878","alleles":["T","C"],"end":140585652,"feature_type":"variation","strand":1,"source":"dbSNP","start":140585652,"consequence_type":"synonymous_variant","assembly_name":"GRCh38"},{"id":"rs768968069","seq_region_name":"7","clinical_significance":[],"start":140585656,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140585656,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"id":"rs61737090","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140585657,"strand":1,"feature_type":"variation","start":140585657,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant"},{"strand":1,"feature_type":"variation","end":140585659,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140585659,"source":"dbSNP","id":"rs1798750317","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140585660,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140585660,"source":"dbSNP","id":"rs1278886425","seq_region_name":"7","clinical_significance":["uncertain significance"]},{"seq_region_name":"7","id":"rs990870218","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140585662,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140585662},{"start":140585663,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140585663,"alleles":["G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs762173823","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140585665,"alleles":["C","G"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585665,"clinical_significance":[],"seq_region_name":"7","id":"rs2130645319"},{"seq_region_name":"7","id":"rs1798750831","clinical_significance":[],"alleles":["A","G"],"end":140585667,"strand":1,"feature_type":"variation","start":140585667,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant"},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585668,"feature_type":"variation","strand":1,"end":140585668,"alleles":["T","A","C"],"clinical_significance":["uncertain significance"],"id":"rs909972902","seq_region_name":"7"},{"source":"dbSNP","start":140585669,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140585669,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1188662482"},{"source":"dbSNP","start":140585671,"consequence_type":"stop_gained","assembly_name":"GRCh38","alleles":["A","C"],"end":140585671,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1260157728","seq_region_name":"7"},{"id":"rs772241395","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140585673,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140585673},{"start":140585674,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["T","C"],"end":140585674,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs776967749","clinical_significance":[]},{"seq_region_name":"7","id":"rs773432539","clinical_significance":[],"strand":1,"feature_type":"variation","end":140585675,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140585675,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs544674444","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585676,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140585676},{"clinical_significance":[],"seq_region_name":"7","id":"rs752648671","alleles":["T","C"],"end":140585678,"feature_type":"variation","strand":1,"source":"dbSNP","start":140585678,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585679,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140585679,"clinical_significance":[],"seq_region_name":"7","id":"rs375091774"},{"seq_region_name":"7","id":"rs1429731195","clinical_significance":[],"strand":1,"feature_type":"variation","end":140585683,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140585683,"source":"dbSNP"},{"start":140585685,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","end":140585685,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1359599540","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs927828917","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585687,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140585687},{"clinical_significance":[],"id":"rs763847757","seq_region_name":"7","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585689,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140585689},{"strand":1,"feature_type":"variation","end":140585690,"alleles":["G","C","T"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140585690,"source":"dbSNP","seq_region_name":"7","id":"rs751166833","clinical_significance":[]},{"end":140585691,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140585691,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs200051101","seq_region_name":"7"},{"seq_region_name":"7","id":"rs772656922","clinical_significance":[],"start":140585694,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"inframe_deletion","alleles":["CTCCT","CT"],"end":140585698,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140585696,"alleles":["C","G","T"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585696,"clinical_significance":[],"seq_region_name":"7","id":"rs1798753275"},{"clinical_significance":[],"seq_region_name":"7","id":"rs142905722","end":140585697,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140585697,"consequence_type":"synonymous_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140585698,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140585698,"source":"dbSNP","id":"rs1381408367","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs868103441","seq_region_name":"7","end":140585700,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140585700,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"end":140585701,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140585701,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs1283881636","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140585702,"alleles":["T","C"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585702,"clinical_significance":["uncertain significance"],"id":"rs749944873","seq_region_name":"7"},{"seq_region_name":"7","id":"rs755674909","clinical_significance":[],"end":140585706,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140585706,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs146125611","source":"dbSNP","start":140585707,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140585707,"feature_type":"variation","strand":1},{"alleles":["G","A"],"end":140585713,"strand":1,"feature_type":"variation","start":140585713,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_region_variant","seq_region_name":"7","id":"rs1798754735","clinical_significance":[]},{"seq_region_name":"7","id":"rs1317587503","clinical_significance":[],"start":140585714,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_region_variant","alleles":["T","C"],"end":140585714,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1798754950","seq_region_name":"7","source":"dbSNP","start":140585717,"consequence_type":"splice_region_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140585717,"feature_type":"variation","strand":1},{"start":140585722,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_polypyrimidine_tract_variant","alleles":["G","C"],"end":140585722,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1478869934","clinical_significance":[]},{"clinical_significance":[],"id":"rs1280548658","seq_region_name":"7","source":"dbSNP","start":140585723,"consequence_type":"splice_polypyrimidine_tract_variant","assembly_name":"GRCh38","end":140585723,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798755253","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140585726,"consequence_type":"splice_polypyrimidine_tract_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585726},{"clinical_significance":[],"seq_region_name":"7","id":"rs749798989","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140585728,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585728},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140585729,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585729,"source":"dbSNP","seq_region_name":"7","id":"rs73736619","clinical_significance":[]},{"seq_region_name":"7","id":"rs1186513680","clinical_significance":[],"strand":1,"feature_type":"variation","end":140585730,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585730,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs779166477","source":"dbSNP","start":140585738,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140585738,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798755881","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585739,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140585739},{"strand":1,"feature_type":"variation","end":140585742,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585742,"source":"dbSNP","seq_region_name":"7","id":"rs1563159681","clinical_significance":[]},{"source":"dbSNP","start":140585746,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140585746,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1798756119","seq_region_name":"7"},{"source":"dbSNP","start":140585748,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140585748,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798756249"},{"id":"rs1203011601","seq_region_name":"7","clinical_significance":[],"end":140585749,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140585749,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140585759,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140585759,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1223623228","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1798756741","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585760,"feature_type":"variation","strand":1,"end":140585759,"alleles":["-","A"]},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140585760,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585760,"clinical_significance":[],"seq_region_name":"7","id":"rs1563159685"},{"end":140585762,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140585762,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798756943","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585765,"feature_type":"variation","strand":1,"end":140585765,"alleles":["T","C"],"clinical_significance":[],"id":"rs1239517707","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585768,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140585768,"clinical_significance":[],"seq_region_name":"7","id":"rs1433514834"},{"end":140585775,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140585775,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs942879180","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140585779,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585779,"source":"dbSNP","seq_region_name":"7","id":"rs1798757438","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs369301088","feature_type":"variation","strand":1,"end":140585815,"alleles":["GTCAGTATCTTGGCCTCTCCTGTGTCCATTCTTGTAG","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585779},{"id":"rs1262146683","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585780,"source":"dbSNP","strand":1,"feature_type":"variation","end":140585780,"alleles":["T","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs148795201","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140585784,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585784},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585785,"feature_type":"variation","strand":1,"end":140585785,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1198702064"},{"strand":1,"feature_type":"variation","end":140585788,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585788,"source":"dbSNP","seq_region_name":"7","id":"rs1038719695","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585694038","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585791,"source":"dbSNP","strand":1,"feature_type":"variation","end":140585791,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798758278","source":"dbSNP","start":140585792,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140585792,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1798758388","clinical_significance":[],"start":140585794,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140585794,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140585798,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585798,"source":"dbSNP","seq_region_name":"7","id":"rs142483349","clinical_significance":[]},{"id":"rs1213976481","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585800,"source":"dbSNP","strand":1,"feature_type":"variation","end":140585800,"alleles":["G","C"]},{"start":140585806,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140585806,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798758745","clinical_significance":[]},{"seq_region_name":"7","id":"rs1011105221","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585812,"source":"dbSNP","strand":1,"feature_type":"variation","end":140585812,"alleles":["G","A"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585817,"source":"dbSNP","strand":1,"feature_type":"variation","end":140585817,"alleles":["C","G","T"],"seq_region_name":"7","id":"rs75640774","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140585820,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585820,"source":"dbSNP","id":"rs1450207474","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798759260","alleles":["T","C"],"end":140585821,"feature_type":"variation","strand":1,"source":"dbSNP","start":140585821,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585834,"feature_type":"variation","strand":1,"end":140585834,"alleles":["C","T"],"clinical_significance":[],"id":"rs887228599","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs940088368","source":"dbSNP","start":140585837,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140585837,"alleles":["C","A"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585839,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","T"],"end":140585839,"seq_region_name":"7","id":"rs1041492596","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs532588099","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140585840,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585840},{"seq_region_name":"7","id":"rs115951091","clinical_significance":[],"start":140585842,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","T"],"end":140585842,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585843,"feature_type":"variation","strand":1,"end":140585843,"alleles":["G","A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs370687047"},{"id":"rs1798760129","seq_region_name":"7","clinical_significance":[],"start":140585847,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140585847,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140585851,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140585851,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs569223580","seq_region_name":"7"},{"start":140585852,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140585852,"alleles":["G","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798760373","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130645828","source":"dbSNP","start":140585856,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140585856,"feature_type":"variation","strand":1},{"end":140585859,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140585859,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1585694164","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1406391832","feature_type":"variation","strand":1,"end":140585861,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585861},{"clinical_significance":[],"seq_region_name":"7","id":"rs73498497","source":"dbSNP","start":140585863,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140585863,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1798760826","seq_region_name":"7","alleles":["C","T"],"end":140585864,"feature_type":"variation","strand":1,"source":"dbSNP","start":140585864,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140585865,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140585865,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs2130645883","seq_region_name":"7"},{"id":"rs894053786","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585866,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140585866},{"seq_region_name":"7","id":"rs1798761037","clinical_significance":[],"alleles":["C","-"],"end":140585875,"strand":1,"feature_type":"variation","start":140585875,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1182082636","feature_type":"variation","strand":1,"end":140585885,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585885},{"seq_region_name":"7","id":"rs1798761263","clinical_significance":[],"start":140585886,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140585886,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1444459201","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140585887,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585887},{"strand":1,"feature_type":"variation","end":140585889,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585889,"source":"dbSNP","id":"rs1242110510","seq_region_name":"7","clinical_significance":[]},{"end":140585897,"alleles":["CTCCTC","CTC"],"strand":1,"feature_type":"variation","start":140585892,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1798761570","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1010569313","alleles":["C","T"],"end":140585894,"feature_type":"variation","strand":1,"source":"dbSNP","start":140585894,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1020581092","clinical_significance":[],"start":140585895,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140585895,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585899,"feature_type":"variation","strand":1,"end":140585899,"alleles":["T","C"],"clinical_significance":[],"id":"rs1798761933","seq_region_name":"7"},{"end":140585900,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","start":140585900,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1016813123","clinical_significance":[]},{"seq_region_name":"7","id":"rs1203216324","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585901,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140585901},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585909,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140585909,"clinical_significance":[],"id":"rs1322201390","seq_region_name":"7"},{"start":140585910,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140585910,"alleles":["G","T"],"strand":1,"feature_type":"variation","id":"rs1286802227","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798762606","end":140585923,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140585923,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140585938,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140585938,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs966317741","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs368331510","feature_type":"variation","strand":1,"end":140585939,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585939},{"start":140585941,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140585941,"alleles":["T","G"],"strand":1,"feature_type":"variation","id":"rs962775223","seq_region_name":"7","clinical_significance":[]},{"id":"rs1449201278","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585943,"source":"dbSNP","strand":1,"feature_type":"variation","end":140585943,"alleles":["T","A"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585944,"feature_type":"variation","strand":1,"end":140585944,"alleles":["A","G"],"clinical_significance":[],"id":"rs1451910341","seq_region_name":"7"},{"end":140585945,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140585945,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1195274124","clinical_significance":[]},{"source":"dbSNP","start":140585947,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140585947,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798763442"},{"seq_region_name":"7","id":"rs981842171","clinical_significance":[],"start":140585948,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140585948,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1585694422","clinical_significance":[],"start":140585951,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140585951,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140585956,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585956,"clinical_significance":[],"id":"rs1798763777","seq_region_name":"7"},{"source":"dbSNP","start":140585958,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140585958,"alleles":["T","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1437312173"},{"seq_region_name":"7","id":"rs139482423","clinical_significance":[],"start":140585959,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140585959,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585969,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140585969,"seq_region_name":"7","id":"rs1035156662","clinical_significance":[]},{"clinical_significance":[],"id":"rs1352101698","seq_region_name":"7","alleles":["C","T"],"end":140585971,"feature_type":"variation","strand":1,"source":"dbSNP","start":140585971,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140585975,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140585975,"clinical_significance":[],"seq_region_name":"7","id":"rs1798764287"},{"seq_region_name":"7","id":"rs2130646090","clinical_significance":[],"start":140585982,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140585982,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140585988,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585988,"source":"dbSNP","seq_region_name":"7","id":"rs1162267577","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1393138490","end":140585995,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140585995,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140585996,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585996,"source":"dbSNP","id":"rs1798764652","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140585999,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140585999,"seq_region_name":"7","id":"rs959256539","clinical_significance":[]},{"end":140586002,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140586002,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1798764916","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","A"],"end":140586008,"strand":1,"feature_type":"variation","start":140586008,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1160842436","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140586009,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586009,"source":"dbSNP","seq_region_name":"7","id":"rs534117066","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586010,"feature_type":"variation","strand":1,"end":140586010,"alleles":["C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1798765159"},{"seq_region_name":"7","id":"rs553077938","clinical_significance":[],"start":140586014,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140586014,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1248021702","feature_type":"variation","strand":1,"end":140586024,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586024},{"id":"rs1159216912","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586026,"source":"dbSNP","strand":1,"feature_type":"variation","end":140586026,"alleles":["C","A","T"]},{"alleles":["A","G"],"end":140586027,"feature_type":"variation","strand":1,"source":"dbSNP","start":140586027,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs973252341"},{"seq_region_name":"7","id":"rs577697461","clinical_significance":[],"end":140586028,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140586028,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130646174","alleles":["A","T"],"end":140586032,"feature_type":"variation","strand":1,"source":"dbSNP","start":140586032,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563159854","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586033,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140586033},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798765993","alleles":["C","T"],"end":140586035,"feature_type":"variation","strand":1,"source":"dbSNP","start":140586035,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1585694580","clinical_significance":[],"alleles":["C","T"],"end":140586036,"strand":1,"feature_type":"variation","start":140586036,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs920556232","clinical_significance":[],"start":140586038,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","G","T"],"end":140586038,"strand":1,"feature_type":"variation"},{"alleles":["G","A","T"],"end":140586039,"strand":1,"feature_type":"variation","start":140586039,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1451069095","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","T"],"end":140586041,"feature_type":"variation","strand":1,"source":"dbSNP","start":140586041,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs186389204"},{"clinical_significance":[],"seq_region_name":"7","id":"rs556651094","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586048,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140586048},{"end":140586049,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140586049,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798766763","clinical_significance":[]},{"id":"rs1286381705","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586051,"source":"dbSNP","strand":1,"feature_type":"variation","end":140586051,"alleles":["G","C"]},{"clinical_significance":[],"id":"rs2130646239","seq_region_name":"7","source":"dbSNP","start":140586053,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140586053,"alleles":["A","G"],"feature_type":"variation","strand":1},{"id":"rs575632822","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140586054,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586054,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1240950663","clinical_significance":[],"end":140586056,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140586056,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs2130646264","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586058,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140586058},{"end":140586061,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140586061,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs987035988","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140586069,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586069,"clinical_significance":[],"seq_region_name":"7","id":"rs1306622636"},{"seq_region_name":"7","id":"rs542896733","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586070,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140586070},{"id":"rs1347539860","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140586075,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586075,"source":"dbSNP"},{"alleles":["T","C"],"end":140586076,"strand":1,"feature_type":"variation","start":140586076,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130646312","clinical_significance":[]},{"id":"rs1563159878","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586080,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140586080},{"end":140586082,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140586082,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs911475561"},{"clinical_significance":[],"id":"rs1798767884","seq_region_name":"7","source":"dbSNP","start":140586086,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140586086,"alleles":["C","T"],"feature_type":"variation","strand":1},{"alleles":["C","T"],"end":140586087,"feature_type":"variation","strand":1,"source":"dbSNP","start":140586087,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1798767980","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586091,"source":"dbSNP","strand":1,"feature_type":"variation","end":140586091,"alleles":["G","C"],"seq_region_name":"7","id":"rs1798768083","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586097,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140586097,"clinical_significance":[],"id":"rs73498501","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1387665340","clinical_significance":[],"start":140586098,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140586098,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1300397086","source":"dbSNP","start":140586099,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140586099,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs780671462","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140586106,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586106},{"clinical_significance":[],"seq_region_name":"7","id":"rs1328374798","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586107,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140586107},{"clinical_significance":[],"seq_region_name":"7","id":"rs748811469","alleles":["G","A","T"],"end":140586113,"feature_type":"variation","strand":1,"source":"dbSNP","start":140586113,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs114069244","source":"dbSNP","start":140586115,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140586115,"alleles":["T","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs768224941","end":140586118,"alleles":["C","A","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140586118,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586120,"source":"dbSNP","strand":1,"feature_type":"variation","end":140586120,"alleles":["G","A"],"seq_region_name":"7","id":"rs1798769103","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1158002039","source":"dbSNP","start":140586121,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140586121,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798769307","feature_type":"variation","strand":1,"end":140586128,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586128},{"strand":1,"feature_type":"variation","end":140586129,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586129,"source":"dbSNP","seq_region_name":"7","id":"rs1585694816","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586130,"feature_type":"variation","strand":1,"end":140586130,"alleles":["C","A","T"],"clinical_significance":[],"id":"rs80102225","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["AA","A"],"end":140586139,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586138,"source":"dbSNP","id":"rs1798769632","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs922666400","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140586140,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586140,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798769845","end":140586143,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140586143,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1798769953","seq_region_name":"7","clinical_significance":[],"alleles":["T","A"],"end":140586144,"strand":1,"feature_type":"variation","start":140586144,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1798770071","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586145,"source":"dbSNP","strand":1,"feature_type":"variation","end":140586145,"alleles":["G","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1430719370","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140586153,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586153},{"id":"rs2130646464","seq_region_name":"7","clinical_significance":[],"start":140586154,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140586154,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs574498330","end":140586160,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140586160,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140586162,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C","G"],"end":140586162,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585694860","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140586164,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586164,"clinical_significance":[],"id":"rs1585694869","seq_region_name":"7"},{"end":140586166,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140586166,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798770687"},{"start":140586169,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","T"],"end":140586169,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798770802","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140586170,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586170,"source":"dbSNP","id":"rs1003625004","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","T"],"end":140586180,"feature_type":"variation","strand":1,"source":"dbSNP","start":140586180,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798771081"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140586181,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586181,"source":"dbSNP","seq_region_name":"7","id":"rs1206652216","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586183,"feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140586183,"clinical_significance":[],"seq_region_name":"7","id":"rs1260297737"},{"end":140586187,"alleles":["A","G","T"],"strand":1,"feature_type":"variation","start":140586187,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1050347628","clinical_significance":[]},{"source":"dbSNP","start":140586189,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140586189,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798771644"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585694905","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586190,"feature_type":"variation","strand":1,"end":140586190,"alleles":["C","A","G"]},{"id":"rs895057192","seq_region_name":"7","clinical_significance":[],"end":140586194,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140586194,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["A","G"],"end":140586202,"strand":1,"feature_type":"variation","start":140586202,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs144218654","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","A"],"end":140586205,"feature_type":"variation","strand":1,"source":"dbSNP","start":140586205,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1012201039"},{"start":140586207,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140586207,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs893938391","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1325948738","clinical_significance":[],"alleles":["G","A"],"end":140586213,"strand":1,"feature_type":"variation","start":140586213,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140586215,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140586215,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1467916626"},{"start":140586223,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AAA","AA"],"end":140586225,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1223020740","clinical_significance":[]},{"start":140586226,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140586226,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1563159949","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1016758619","source":"dbSNP","start":140586235,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140586235,"alleles":["G","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798772925","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586236,"feature_type":"variation","strand":1,"end":140586236,"alleles":["G","C"]},{"start":140586238,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140586238,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1179164230","clinical_significance":[]},{"source":"dbSNP","start":140586242,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140586242,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs113656447","seq_region_name":"7"},{"id":"rs190327633","seq_region_name":"7","clinical_significance":[],"end":140586246,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140586246,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140586247,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140586247,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs753652238","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586252,"feature_type":"variation","strand":1,"end":140586252,"alleles":["C","T"],"clinical_significance":[],"id":"rs1585695023","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1157769784","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586256,"feature_type":"variation","strand":1,"end":140586256,"alleles":["C","T"]},{"strand":1,"feature_type":"variation","end":140586256,"alleles":["C","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586256,"source":"dbSNP","id":"rs1798773814","seq_region_name":"7","clinical_significance":[]},{"start":140586257,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140586257,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585695047","clinical_significance":[]},{"source":"dbSNP","start":140586259,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140586259,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798774064"},{"source":"dbSNP","start":140586260,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140586260,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1585695055","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585695070","source":"dbSNP","start":140586261,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140586261,"alleles":["G","A"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140586263,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586263,"source":"dbSNP","seq_region_name":"7","id":"rs1798774408","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140586267,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586267,"clinical_significance":[],"seq_region_name":"7","id":"rs902208323"},{"end":140586270,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140586270,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798774625","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586271,"source":"dbSNP","strand":1,"feature_type":"variation","end":140586271,"alleles":["G","A","C"],"seq_region_name":"7","id":"rs955362094","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1195327953","feature_type":"variation","strand":1,"end":140586273,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586273},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585695105","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140586275,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586275},{"clinical_significance":[],"id":"rs374224594","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586279,"feature_type":"variation","strand":1,"end":140586279,"alleles":["G","A"]},{"source":"dbSNP","start":140586282,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140586282,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585695122"},{"seq_region_name":"7","id":"rs1260709130","clinical_significance":[],"start":140586283,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140586283,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"alleles":["C","T"],"end":140586284,"feature_type":"variation","strand":1,"source":"dbSNP","start":140586284,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs911253841"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586285,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140586285,"id":"rs548509706","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586288,"feature_type":"variation","strand":1,"end":140586288,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585695162"},{"clinical_significance":[],"seq_region_name":"7","id":"rs368908596","source":"dbSNP","start":140586289,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140586289,"alleles":["G","A","C","T"],"feature_type":"variation","strand":1},{"alleles":["G","C","T"],"end":140586290,"strand":1,"feature_type":"variation","start":140586290,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1318775915","seq_region_name":"7","clinical_significance":[]},{"end":140586291,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140586291,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1440711220"},{"seq_region_name":"7","id":"rs1798776292","clinical_significance":[],"strand":1,"feature_type":"variation","end":140586292,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586292,"source":"dbSNP"},{"start":140586294,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140586294,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1253578671","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","CC","CCAC"],"end":140586298,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586298,"clinical_significance":[],"seq_region_name":"7","id":"rs1332567260"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1326362027","alleles":["A","C"],"end":140586299,"feature_type":"variation","strand":1,"source":"dbSNP","start":140586299,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1376176415","clinical_significance":[],"alleles":["C","CCC"],"end":140586300,"strand":1,"feature_type":"variation","start":140586300,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140586300,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140586300,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798776781","clinical_significance":[]},{"seq_region_name":"7","id":"rs1313833294","clinical_significance":[],"end":140586303,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140586303,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140586310,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586310,"source":"dbSNP","seq_region_name":"7","id":"rs1798777114","clinical_significance":[]},{"start":140586313,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140586313,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798777234","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140586315,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586315,"source":"dbSNP","seq_region_name":"7","id":"rs1012118984","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs778594112","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586316,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140586316},{"id":"rs1334331382","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140586326,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586326,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798777651","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586328,"feature_type":"variation","strand":1,"end":140586328,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798777764","feature_type":"variation","strand":1,"end":140586335,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586335},{"seq_region_name":"7","id":"rs1468832204","clinical_significance":[],"alleles":["G","T"],"end":140586338,"strand":1,"feature_type":"variation","start":140586338,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["A","C"],"end":140586343,"strand":1,"feature_type":"variation","start":140586343,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798777966","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1341183406","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586344,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140586344},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586345,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140586345,"clinical_significance":[],"id":"rs1169158509","seq_region_name":"7"},{"end":140586346,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140586346,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1798778324","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs527914022","feature_type":"variation","strand":1,"end":140586347,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586347},{"source":"dbSNP","start":140586348,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140586348,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs983379318"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140586350,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586350,"clinical_significance":[],"id":"rs1585695349","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798779078","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140586352,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586352},{"seq_region_name":"7","id":"rs1563160029","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["AAAAAA","AAAAA"],"end":140586362,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586357,"source":"dbSNP"},{"source":"dbSNP","start":140586361,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140586361,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs552478537"},{"end":140586363,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140586363,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1241521959","clinical_significance":[]},{"seq_region_name":"7","id":"rs1199042132","clinical_significance":[],"alleles":["AAAA","AAAAAA"],"end":140586367,"strand":1,"feature_type":"variation","start":140586364,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586364,"feature_type":"variation","strand":1,"alleles":["AAAACA","-"],"end":140586369,"clinical_significance":[],"seq_region_name":"7","id":"rs1390552805"},{"feature_type":"variation","strand":1,"end":140586365,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586365,"clinical_significance":[],"seq_region_name":"7","id":"rs1798779993"},{"alleles":["A","ACACACA"],"end":140586365,"feature_type":"variation","strand":1,"source":"dbSNP","start":140586365,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798780182"},{"alleles":["A","C"],"end":140586366,"feature_type":"variation","strand":1,"source":"dbSNP","start":140586366,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1335986632","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1554474425","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586366,"source":"dbSNP","strand":1,"feature_type":"variation","end":140586369,"alleles":["AACA","AACAACA"]},{"source":"dbSNP","start":140586367,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","AAACA","AAACACA","AAACACACA"],"end":140586367,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs71522104","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586367,"feature_type":"variation","strand":1,"end":140586407,"alleles":["ACACACACACACACACACACACACACACACACACACACACA","ACACACACACACACACACA","ACACACACACACACACACACA","ACACACACACACACACACACACA","ACACACACACACACACACACACACA","ACACACACACACACACACACACACACA","ACACACACACACACACACACACACACACA","ACACACACACACACACACACACACACACACA","ACACACACACACACACACACACACACACACACA","ACACACACACACACACACACACACACACACACACA","ACACACACACACACACACACACACACACACACACACA","ACACACACACACACACACACACACACACACACACACACA","ACACACACACACACACACACACACACACACACACACACACACA","ACACACACACACACACACACACACACACACACACACACACACACA","ACACACACACACACACACACACACACACACACACACACACACACACA","ACACACACACACACACACACACACACACACACACACACACACACACACA","ACACACACACACACACACACACACACACACACACACACACACACACACACA","ACACACACACACACACACACACACACACACACACACACACACACACACACACA","ACACACACACACACACACACACACACACACACACACACACACACACACACACACA","ACACACACACACACACACACACACACACACACACACACACACACACACACACACACA","ACACACACACACACACACACACACACACACACACACACACACACACACACACACACACA"],"clinical_significance":[],"seq_region_name":"7","id":"rs10524571"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586368,"feature_type":"variation","strand":1,"end":140586368,"alleles":["C","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs76229956"},{"seq_region_name":"7","id":"rs1056130514","clinical_significance":[],"start":140586368,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140586368,"alleles":["C","-"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs977150180","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586370,"feature_type":"variation","strand":1,"end":140586370,"alleles":["C","A","T"]},{"end":140586370,"alleles":["C","-"],"strand":1,"feature_type":"variation","start":140586370,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1554474436","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586370,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CACAC","-"],"end":140586374,"seq_region_name":"7","id":"rs1798782243","clinical_significance":[]},{"start":140586370,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["CACACACAC","-"],"end":140586378,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1563160088","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586370,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CACACACACACAC","-"],"end":140586382,"seq_region_name":"7","id":"rs1798782472","clinical_significance":[]},{"seq_region_name":"7","id":"rs922751118","clinical_significance":[],"start":140586372,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140586372,"alleles":["C","A","T"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586374,"feature_type":"variation","strand":1,"end":140586374,"alleles":["C","A","T"],"clinical_significance":[],"id":"rs1241372032","seq_region_name":"7"},{"alleles":["A","G"],"end":140586375,"strand":1,"feature_type":"variation","start":140586375,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs932731615","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130647158","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586375,"source":"dbSNP","strand":1,"feature_type":"variation","end":140586375,"alleles":["A","-"]},{"seq_region_name":"7","id":"rs1798782992","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586376,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140586376},{"clinical_significance":[],"seq_region_name":"7","id":"rs72045424","source":"dbSNP","start":140586377,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["-","CA"],"end":140586376,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1798783199","seq_region_name":"7","alleles":["A","G"],"end":140586377,"feature_type":"variation","strand":1,"source":"dbSNP","start":140586377,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140586378,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140586378,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1350884325"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586380,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140586380,"seq_region_name":"7","id":"rs1798783511","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140586381,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586381,"clinical_significance":[],"seq_region_name":"7","id":"rs1798783664"},{"seq_region_name":"7","id":"rs1416737866","clinical_significance":[],"start":140586382,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140586382,"alleles":["C","CC"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1798783812","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586382,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140586382},{"clinical_significance":[],"seq_region_name":"7","id":"rs1461193868","alleles":["A","ATA"],"end":140586383,"feature_type":"variation","strand":1,"source":"dbSNP","start":140586383,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1798784308","clinical_significance":[],"alleles":["C","A"],"end":140586384,"strand":1,"feature_type":"variation","start":140586384,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1049803187","seq_region_name":"7","clinical_significance":[],"end":140586385,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140586385,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["C","A"],"end":140586388,"feature_type":"variation","strand":1,"source":"dbSNP","start":140586388,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1280984000"},{"seq_region_name":"7","id":"rs894836620","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140586389,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586389,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1460887793","source":"dbSNP","start":140586393,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","AAA"],"end":140586393,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1798785203","clinical_significance":[],"start":140586395,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140586395,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"end":140586395,"alleles":["A","ATA"],"strand":1,"feature_type":"variation","start":140586395,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1798785388","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585695785","clinical_significance":[],"alleles":["C","A"],"end":140586396,"strand":1,"feature_type":"variation","start":140586396,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140586397,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140586409,"alleles":["ACACACACACAAA","ACACACACACAAACACACACACAAA"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798785612"},{"alleles":["A","G"],"end":140586399,"strand":1,"feature_type":"variation","start":140586399,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798785730","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["ACACACACAAA","A"],"end":140586409,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586399,"source":"dbSNP","seq_region_name":"7","id":"rs1303239839","clinical_significance":[]},{"end":140586400,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140586400,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs947928416"},{"clinical_significance":[],"id":"rs1406620765","seq_region_name":"7","source":"dbSNP","start":140586400,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140586400,"alleles":["C","CGC"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1298169290","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140586401,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586401},{"alleles":["ACACACAAA","A"],"end":140586409,"feature_type":"variation","strand":1,"source":"dbSNP","start":140586401,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1363668053","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140586403,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586403,"source":"dbSNP","seq_region_name":"7","id":"rs1798786374","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["ACACAAA","A"],"end":140586409,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586403,"source":"dbSNP","seq_region_name":"7","id":"rs1798786503","clinical_significance":[]},{"end":140586405,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140586405,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798786620"},{"seq_region_name":"7","id":"rs1401122646","clinical_significance":[],"alleles":["ACAAA","A"],"end":140586409,"strand":1,"feature_type":"variation","start":140586405,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1410401284","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586406,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140586406},{"clinical_significance":[],"seq_region_name":"7","id":"rs71173213","feature_type":"variation","strand":1,"end":140586407,"alleles":["A","ACACAAA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586407},{"end":140586409,"alleles":["AAA","A"],"strand":1,"feature_type":"variation","start":140586407,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1491414273","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["-","C","CACAC"],"end":140586407,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586408,"source":"dbSNP","seq_region_name":"7","id":"rs1798787042","clinical_significance":[]},{"seq_region_name":"7","id":"rs915425164","clinical_significance":[],"end":140586408,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140586408,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798787183","end":140586408,"alleles":["-","CACACAC"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140586409,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130647385","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586418,"feature_type":"variation","strand":1,"end":140586418,"alleles":["G","A"]},{"start":140586421,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140586421,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1469680624","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1038307080","source":"dbSNP","start":140586424,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140586424,"alleles":["T","-"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586424,"feature_type":"variation","strand":1,"end":140586424,"alleles":["T","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585695901"},{"source":"dbSNP","start":140586426,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140586426,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs571334528"},{"id":"rs1479720550","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586428,"source":"dbSNP","strand":1,"feature_type":"variation","end":140586428,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs2130647427","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140586430,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586430,"source":"dbSNP"},{"id":"rs1368140121","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140586431,"strand":1,"feature_type":"variation","start":140586431,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140586432,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140586432,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1217781977","clinical_significance":[]},{"start":140586441,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","G"],"end":140586441,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798787974","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs113973120","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140586445,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586445},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130647461","source":"dbSNP","start":140586449,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140586449,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1291595311","source":"dbSNP","start":140586456,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140586456,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1355096138","clinical_significance":[],"start":140586460,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140586460,"alleles":["G","A","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1202936927","end":140586465,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140586465,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1349505992","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586467,"source":"dbSNP","strand":1,"feature_type":"variation","end":140586467,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs994408345","clinical_significance":[],"strand":1,"feature_type":"variation","end":140586468,"alleles":["A","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586468,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140586472,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586472,"source":"dbSNP","id":"rs1798788775","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130647519","clinical_significance":[],"start":140586473,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140586473,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs556999823","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140586474,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586474,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140586476,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586476,"clinical_significance":[],"seq_region_name":"7","id":"rs1798789039"},{"clinical_significance":[],"seq_region_name":"7","id":"rs375953511","source":"dbSNP","start":140586481,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140586481,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1218960405","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140586483,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586483},{"end":140586489,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140586489,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798789404"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586490,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140586490,"clinical_significance":[],"seq_region_name":"7","id":"rs536244569"},{"clinical_significance":[],"seq_region_name":"7","id":"rs554953071","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140586491,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586491},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586495,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140586495,"id":"rs1056529956","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586496,"source":"dbSNP","strand":1,"feature_type":"variation","end":140586496,"alleles":["C","G"],"seq_region_name":"7","id":"rs1400275394","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140586499,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586499,"clinical_significance":[],"seq_region_name":"7","id":"rs891195821"},{"clinical_significance":[],"id":"rs1585696131","seq_region_name":"7","source":"dbSNP","start":140586506,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140586506,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140586507,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586507,"source":"dbSNP","seq_region_name":"7","id":"rs894770512","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140586508,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586508,"clinical_significance":[],"seq_region_name":"7","id":"rs1798790150"},{"strand":1,"feature_type":"variation","end":140586511,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586511,"source":"dbSNP","id":"rs1798790255","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1178620911","clinical_significance":[],"end":140586514,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140586514,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1012417190","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586518,"source":"dbSNP","strand":1,"feature_type":"variation","end":140586518,"alleles":["C","T"]},{"alleles":["G","A"],"end":140586519,"strand":1,"feature_type":"variation","start":140586519,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs573155038","clinical_significance":[]},{"start":140586522,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140586522,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798790724","clinical_significance":[]},{"seq_region_name":"7","id":"rs6971144","clinical_significance":[],"end":140586523,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140586523,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1486336416","alleles":["C","G"],"end":140586525,"feature_type":"variation","strand":1,"source":"dbSNP","start":140586525,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1798791107","clinical_significance":[],"strand":1,"feature_type":"variation","end":140586526,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586526,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140586527,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586527,"source":"dbSNP","seq_region_name":"7","id":"rs1798791217","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs964030874","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586530,"feature_type":"variation","strand":1,"end":140586530,"alleles":["G","C"]},{"feature_type":"variation","strand":1,"end":140586534,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586534,"clinical_significance":[],"seq_region_name":"7","id":"rs1240652612"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586536,"source":"dbSNP","strand":1,"feature_type":"variation","end":140586536,"alleles":["C","G"],"seq_region_name":"7","id":"rs1798791531","clinical_significance":[]},{"source":"dbSNP","start":140586538,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140586538,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1208112317"},{"end":140586540,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140586540,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1256321849"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585696245","source":"dbSNP","start":140586541,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C","G"],"end":140586541,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140586550,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140586550,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1263425224"},{"id":"rs1798792077","seq_region_name":"7","clinical_significance":[],"start":140586552,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140586552,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"id":"rs1563160235","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586556,"source":"dbSNP","strand":1,"feature_type":"variation","end":140586561,"alleles":["AAAAAA","AAAAA"]},{"start":140586556,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140586575,"alleles":["AAAAAATAAAAAATAAAAAA","AAAAAATAAAAAA","AAAAAATAAAAAATAAAAAATAAAAAA"],"strand":1,"feature_type":"variation","id":"rs990330808","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","C","G"],"end":140586560,"feature_type":"variation","strand":1,"source":"dbSNP","start":140586560,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798792439"},{"source":"dbSNP","start":140586561,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140586561,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs28502823"},{"clinical_significance":[],"seq_region_name":"7","id":"rs28555150","end":140586562,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140586562,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140586568,"alleles":["AAAAAA","AAAAAAA"],"strand":1,"feature_type":"variation","start":140586563,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798792776","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1022300371","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140586564,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586564},{"seq_region_name":"7","id":"rs1798792915","clinical_significance":[],"start":140586567,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140586567,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586568,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140586568,"clinical_significance":[],"id":"rs28441620","seq_region_name":"7"},{"alleles":["T","A","G"],"end":140586569,"feature_type":"variation","strand":1,"source":"dbSNP","start":140586569,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs28615560"},{"id":"rs1798793419","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586570,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AAAAAA","AAA"],"end":140586575},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130647750","source":"dbSNP","start":140586571,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140586571,"feature_type":"variation","strand":1},{"start":140586572,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AAAA","AAAATAGAAAA"],"end":140586575,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798793558","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586573,"feature_type":"variation","strand":1,"alleles":["AAAGAAAGAAAGAAA","AAAGAAAGAAA","AAAGAAAGAAAGAAAGAAA"],"end":140586587,"clinical_significance":[],"seq_region_name":"7","id":"rs928848227"},{"seq_region_name":"7","id":"rs183060831","clinical_significance":[],"end":140586576,"alleles":["G","C","T"],"strand":1,"feature_type":"variation","start":140586576,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1563160264","clinical_significance":[],"alleles":["A","G"],"end":140586577,"strand":1,"feature_type":"variation","start":140586577,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140586578,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140586578,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1004706299","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798794252","clinical_significance":[],"alleles":["G","T"],"end":140586584,"strand":1,"feature_type":"variation","start":140586584,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1468298771","source":"dbSNP","start":140586589,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140586589,"alleles":["G","T"],"feature_type":"variation","strand":1},{"alleles":["T","C","G"],"end":140586593,"strand":1,"feature_type":"variation","start":140586593,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs769128866","seq_region_name":"7","clinical_significance":[]},{"end":140586594,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140586594,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs966355246"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586595,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140586595,"seq_region_name":"7","id":"rs1585696391","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798794732","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586599,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140586599},{"id":"rs1376597084","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140586601,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586601,"source":"dbSNP"},{"start":140586608,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140586608,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs1798794965","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798795085","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586610,"feature_type":"variation","strand":1,"end":140586611,"alleles":["AG","-"]},{"source":"dbSNP","start":140586611,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140586611,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130647861"},{"end":140586621,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140586621,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798795184"},{"end":140586622,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140586622,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798795326","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140586626,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586626,"source":"dbSNP","seq_region_name":"7","id":"rs916221489","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1445658358","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140586628,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586628},{"end":140586629,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140586629,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798795675","clinical_significance":[]},{"clinical_significance":[],"id":"rs1243372216","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586639,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140586639},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798795954","end":140586645,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140586645,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586650,"feature_type":"variation","strand":1,"end":140586650,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1798796037"},{"id":"rs1185112263","seq_region_name":"7","clinical_significance":[],"start":140586654,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140586654,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1798796223","seq_region_name":"7","feature_type":"variation","strand":1,"end":140586657,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586657},{"clinical_significance":[],"seq_region_name":"7","id":"rs975986606","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586658,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140586658},{"start":140586661,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140586661,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs947708793","seq_region_name":"7","clinical_significance":[]},{"end":140586663,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140586663,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1459712385","seq_region_name":"7"},{"start":140586664,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","T"],"end":140586664,"strand":1,"feature_type":"variation","id":"rs147627067","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1798796651","seq_region_name":"7","source":"dbSNP","start":140586667,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140586667,"feature_type":"variation","strand":1},{"start":140586668,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","-"],"end":140586668,"strand":1,"feature_type":"variation","id":"rs1309135186","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140586670,"alleles":["A","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586670,"clinical_significance":[],"seq_region_name":"7","id":"rs1270859880"},{"start":140586676,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140586676,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798796974","clinical_significance":[]},{"alleles":["C","T"],"end":140586686,"strand":1,"feature_type":"variation","start":140586686,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs954044126","clinical_significance":[]},{"clinical_significance":[],"id":"rs1374976424","seq_region_name":"7","feature_type":"variation","strand":1,"end":140586687,"alleles":["G","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586687},{"end":140586688,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140586688,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs766330953","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140586691,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586691,"clinical_significance":[],"seq_region_name":"7","id":"rs149105873"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798797906","alleles":["T","G"],"end":140586697,"feature_type":"variation","strand":1,"source":"dbSNP","start":140586697,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140586702,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586702,"source":"dbSNP","seq_region_name":"7","id":"rs1450632880","clinical_significance":[]},{"start":140586705,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140586705,"alleles":["G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1727234646","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586706,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140586706,"clinical_significance":[],"seq_region_name":"7","id":"rs1798798227"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1290926382","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586708,"feature_type":"variation","strand":1,"end":140586707,"alleles":["-","G"]},{"clinical_significance":[],"id":"rs1359588688","seq_region_name":"7","end":140586719,"alleles":["TCCCGCTGCTT","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140586709,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1047321146","source":"dbSNP","start":140586710,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140586710,"alleles":["C","T"],"feature_type":"variation","strand":1},{"start":140586712,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G","T"],"end":140586712,"strand":1,"feature_type":"variation","id":"rs73736622","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs115158346","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586713,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140586713},{"seq_region_name":"7","id":"rs1798799444","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586716,"source":"dbSNP","strand":1,"feature_type":"variation","end":140586716,"alleles":["G","A"]},{"end":140586724,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140586724,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1231378297"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1018324719","feature_type":"variation","strand":1,"end":140586726,"alleles":["G","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586726},{"seq_region_name":"7","id":"rs1798800017","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586730,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140586730},{"start":140586733,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140586733,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs899807446","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140586734,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586734,"clinical_significance":[],"seq_region_name":"7","id":"rs1162067150"},{"seq_region_name":"7","id":"rs1798800508","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586735,"source":"dbSNP","strand":1,"feature_type":"variation","end":140586735,"alleles":["T","C"]},{"end":140586737,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140586737,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1278950206","clinical_significance":[]},{"seq_region_name":"7","id":"rs978220508","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586740,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140586740},{"source":"dbSNP","start":140586744,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140586744,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1177253863"},{"strand":1,"feature_type":"variation","end":140586749,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586749,"source":"dbSNP","seq_region_name":"7","id":"rs1585696646","clinical_significance":[]},{"clinical_significance":[],"id":"rs1021663319","seq_region_name":"7","alleles":["T","C","G"],"end":140586755,"feature_type":"variation","strand":1,"source":"dbSNP","start":140586755,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586758,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140586758,"seq_region_name":"7","id":"rs1240013724","clinical_significance":[]},{"seq_region_name":"7","id":"rs968022383","clinical_significance":[],"end":140586759,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140586759,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140586766,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140586766,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1485059040"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586776,"source":"dbSNP","strand":1,"feature_type":"variation","end":140586776,"alleles":["A","G","T"],"id":"rs748637147","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140586777,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586777,"source":"dbSNP","seq_region_name":"7","id":"rs1186329653","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586779,"source":"dbSNP","strand":1,"feature_type":"variation","end":140586779,"alleles":["C","T"],"seq_region_name":"7","id":"rs2130648165","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1036244559","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586780,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140586780},{"clinical_significance":[],"id":"rs2130648187","seq_region_name":"7","feature_type":"variation","strand":1,"end":140586784,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586784},{"end":140586786,"alleles":["CC","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140586785,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1798802469","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1798802579","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140586788,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586788},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586801,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140586801,"seq_region_name":"7","id":"rs1321322594","clinical_significance":[]},{"end":140586803,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140586803,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1798802795","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586806,"feature_type":"variation","strand":1,"end":140586806,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130648227"},{"clinical_significance":[],"id":"rs760466478","seq_region_name":"7","source":"dbSNP","start":140586809,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["CC","C"],"end":140586810,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586812,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140586812,"seq_region_name":"7","id":"rs568792887","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586814,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140586814,"clinical_significance":[],"seq_region_name":"7","id":"rs1798803112"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140586816,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586816,"source":"dbSNP","id":"rs1798803224","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1225535489","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140586821,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586821},{"strand":1,"feature_type":"variation","end":140586827,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586827,"source":"dbSNP","seq_region_name":"7","id":"rs1798803425","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798803539","feature_type":"variation","strand":1,"alleles":["ATTGATGATT","ATT"],"end":140586840,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586831},{"end":140586839,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140586839,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1172361361","clinical_significance":[]},{"end":140586842,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140586842,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1371351315"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1394554730","alleles":["A","C"],"end":140586843,"feature_type":"variation","strand":1,"source":"dbSNP","start":140586843,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs939600245","feature_type":"variation","strand":1,"end":140586845,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586845},{"alleles":["G","-"],"end":140586849,"strand":1,"feature_type":"variation","start":140586849,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1563160391","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586850,"feature_type":"variation","strand":1,"end":140586850,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs143203000"},{"feature_type":"variation","strand":1,"end":140586851,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586851,"clinical_significance":[],"seq_region_name":"7","id":"rs1798804366"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798804504","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586854,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140586854},{"id":"rs1368038613","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586859,"source":"dbSNP","strand":1,"feature_type":"variation","end":140586859,"alleles":["A","C","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586860,"source":"dbSNP","strand":1,"feature_type":"variation","end":140586860,"alleles":["T","A"],"seq_region_name":"7","id":"rs1343661442","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs894815757","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586863,"feature_type":"variation","strand":1,"end":140586863,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs1301626832","clinical_significance":[],"alleles":["CAC","CACAC"],"end":140586868,"strand":1,"feature_type":"variation","start":140586866,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1798805310","clinical_significance":[],"strand":1,"feature_type":"variation","end":140586881,"alleles":["CCCTACCTGCCCCT","CCCT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586868,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs916335973","source":"dbSNP","start":140586876,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140586876,"alleles":["G","T"],"feature_type":"variation","strand":1},{"end":140586880,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140586880,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1348911142"},{"id":"rs947722518","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140586885,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586885,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586888,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140586888,"clinical_significance":[],"seq_region_name":"7","id":"rs148276968"},{"clinical_significance":[],"seq_region_name":"7","id":"rs919628916","source":"dbSNP","start":140586892,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140586892,"feature_type":"variation","strand":1},{"end":140586898,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140586898,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs887518886","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1180862076","feature_type":"variation","strand":1,"end":140586899,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586899},{"clinical_significance":[],"seq_region_name":"7","id":"rs1326362374","end":140586900,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140586900,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1798806342","clinical_significance":[],"start":140586902,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TTT","TT"],"end":140586904,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1798806455","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586903,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140586903},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586905,"feature_type":"variation","strand":1,"end":140586905,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1004758929"},{"start":140586910,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140586913,"alleles":["TTTT","TTTTT"],"strand":1,"feature_type":"variation","id":"rs751850685","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586913,"source":"dbSNP","strand":1,"feature_type":"variation","end":140586913,"alleles":["T","C"],"id":"rs1798806773","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140586914,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140586914,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798806888"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586922,"source":"dbSNP","strand":1,"feature_type":"variation","end":140586922,"alleles":["G","T"],"seq_region_name":"7","id":"rs1798807000","clinical_significance":[]},{"seq_region_name":"7","id":"rs1372979792","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586923,"source":"dbSNP","strand":1,"feature_type":"variation","end":140586925,"alleles":["TTT","TT"]},{"alleles":["T","C"],"end":140586928,"feature_type":"variation","strand":1,"source":"dbSNP","start":140586928,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1798807357","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586933,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140586933,"clinical_significance":[],"seq_region_name":"7","id":"rs929863096"},{"seq_region_name":"7","id":"rs1585696998","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586934,"source":"dbSNP","strand":1,"feature_type":"variation","end":140586934,"alleles":["A","C"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586942,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140586942,"seq_region_name":"7","id":"rs1014769208","clinical_significance":[]},{"clinical_significance":[],"id":"rs75708840","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140586944,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586944},{"id":"rs766762327","seq_region_name":"7","clinical_significance":[],"start":140586945,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140586945,"strand":1,"feature_type":"variation"},{"alleles":["A","G"],"end":140586947,"strand":1,"feature_type":"variation","start":140586947,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs997856743","clinical_significance":[]},{"seq_region_name":"7","id":"rs1028888211","clinical_significance":[],"strand":1,"feature_type":"variation","end":140586949,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586949,"source":"dbSNP"},{"seq_region_name":"7","id":"rs774548609","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586950,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140586950},{"feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140586953,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586953,"clinical_significance":[],"seq_region_name":"7","id":"rs532243857"},{"source":"dbSNP","start":140586955,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140586955,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1224228448"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1347916391","source":"dbSNP","start":140586956,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140586956,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586958,"source":"dbSNP","strand":1,"feature_type":"variation","end":140586958,"alleles":["T","C"],"seq_region_name":"7","id":"rs1281976263","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586966,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140586966,"seq_region_name":"7","id":"rs1281648623","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586967,"source":"dbSNP","strand":1,"feature_type":"variation","end":140586967,"alleles":["G","A"],"seq_region_name":"7","id":"rs1386562085","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs943878480","source":"dbSNP","start":140586968,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140586968,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1315989819","clinical_significance":[],"strand":1,"feature_type":"variation","end":140586974,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586974,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1798810267","clinical_significance":[],"start":140586982,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140586982,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs767733912","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586983,"source":"dbSNP","strand":1,"feature_type":"variation","end":140586983,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798810459","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140586984,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586984},{"clinical_significance":[],"seq_region_name":"7","id":"rs1291017288","alleles":["A","C"],"end":140586986,"feature_type":"variation","strand":1,"source":"dbSNP","start":140586986,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140586987,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586987,"source":"dbSNP","seq_region_name":"7","id":"rs1221909042","clinical_significance":[]},{"id":"rs1798810826","seq_region_name":"7","clinical_significance":[],"start":140586988,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140586988,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140586989,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586989,"clinical_significance":[],"seq_region_name":"7","id":"rs796182837"},{"start":140586991,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140586991,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798811181","clinical_significance":[]},{"seq_region_name":"7","id":"rs968099544","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586992,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140586992},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140586994,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140586994,"seq_region_name":"7","id":"rs2130648640","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798811400","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140586995,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140586995},{"seq_region_name":"7","id":"rs978106423","clinical_significance":[],"start":140587003,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140587003,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587004,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140587004,"clinical_significance":[],"id":"rs1798811585","seq_region_name":"7"},{"start":140587007,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140587007,"alleles":["A","T"],"strand":1,"feature_type":"variation","id":"rs1798811691","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587008,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140587008,"clinical_significance":[],"seq_region_name":"7","id":"rs1798811785"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798811893","end":140587012,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140587012,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587017,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140587017,"seq_region_name":"7","id":"rs1798811999","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587023,"source":"dbSNP","strand":1,"feature_type":"variation","end":140587023,"alleles":["A","G"],"seq_region_name":"7","id":"rs1798812118","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798812234","end":140587027,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140587027,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1798812330","clinical_significance":[],"strand":1,"feature_type":"variation","end":140587032,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587032,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140587035,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587035,"source":"dbSNP","seq_region_name":"7","id":"rs1585697206","clinical_significance":[]},{"alleles":["T","G"],"end":140587036,"strand":1,"feature_type":"variation","start":140587036,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798812520","clinical_significance":[]},{"source":"dbSNP","start":140587038,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140587038,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798812640"},{"seq_region_name":"7","id":"rs1798812740","clinical_significance":[],"start":140587042,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140587042,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1798812847","seq_region_name":"7","feature_type":"variation","strand":1,"end":140587043,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587043},{"seq_region_name":"7","id":"rs1585697216","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587044,"source":"dbSNP","strand":1,"feature_type":"variation","end":140587044,"alleles":["C","A"]},{"source":"dbSNP","start":140587052,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140587052,"alleles":["A","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1470163494","seq_region_name":"7"},{"seq_region_name":"7","id":"rs79146459","clinical_significance":[],"start":140587053,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140587053,"alleles":["C","G","T"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140587054,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140587054,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1252936588"},{"clinical_significance":[],"seq_region_name":"7","id":"rs939506030","source":"dbSNP","start":140587055,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140587055,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140587059,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587059,"source":"dbSNP","seq_region_name":"7","id":"rs568973382","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140587060,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587060,"source":"dbSNP","id":"rs1011648683","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140587062,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587062,"clinical_significance":[],"id":"rs1798813751","seq_region_name":"7"},{"id":"rs1798813855","seq_region_name":"7","clinical_significance":[],"alleles":["C","A"],"end":140587063,"strand":1,"feature_type":"variation","start":140587063,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587068,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140587068,"clinical_significance":[],"seq_region_name":"7","id":"rs1197258991"},{"seq_region_name":"7","id":"rs1432536447","clinical_significance":[],"strand":1,"feature_type":"variation","end":140587074,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587074,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798814171","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587075,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140587075},{"start":140587077,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140587077,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1262084514","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587078,"source":"dbSNP","strand":1,"feature_type":"variation","end":140587078,"alleles":["A","G"],"seq_region_name":"7","id":"rs1798814386","clinical_significance":[]},{"seq_region_name":"7","id":"rs557282332","clinical_significance":[],"strand":1,"feature_type":"variation","end":140587081,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587081,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140587082,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587082,"clinical_significance":[],"seq_region_name":"7","id":"rs1798814580"},{"seq_region_name":"7","id":"rs1798814682","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587083,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140587083},{"strand":1,"feature_type":"variation","end":140587090,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587090,"source":"dbSNP","id":"rs1484988630","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798814913","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587092,"feature_type":"variation","strand":1,"end":140587092,"alleles":["C","G"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587094,"source":"dbSNP","strand":1,"feature_type":"variation","end":140587094,"alleles":["G","-"],"seq_region_name":"7","id":"rs1798815013","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798815097","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587099,"feature_type":"variation","strand":1,"end":140587099,"alleles":["C","T"]},{"id":"rs2130648867","seq_region_name":"7","clinical_significance":[],"end":140587100,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140587100,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1798815195","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587105,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140587105},{"clinical_significance":[],"seq_region_name":"7","id":"rs992837816","alleles":["T","C"],"end":140587110,"feature_type":"variation","strand":1,"source":"dbSNP","start":140587110,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140587111,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140587111,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1204355009","clinical_significance":[]},{"start":140587116,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140587116,"alleles":["C","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798815488","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130648899","alleles":["C","T"],"end":140587117,"feature_type":"variation","strand":1,"source":"dbSNP","start":140587117,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140587119,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","T"],"end":140587119,"strand":1,"feature_type":"variation","id":"rs757154152","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587121,"source":"dbSNP","strand":1,"feature_type":"variation","end":140587124,"alleles":["CTCT","CT"],"seq_region_name":"7","id":"rs1261804348","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587123,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140587123,"clinical_significance":[],"seq_region_name":"7","id":"rs1585697422"},{"alleles":["T","TT"],"end":140587124,"strand":1,"feature_type":"variation","start":140587124,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1233093459","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798816026","source":"dbSNP","start":140587128,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","AA"],"end":140587128,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587130,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140587130,"clinical_significance":[],"id":"rs765014202","seq_region_name":"7"},{"start":140587142,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140587142,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs1308608471","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1298115807","clinical_significance":[],"start":140587147,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","-"],"end":140587147,"strand":1,"feature_type":"variation"},{"start":140587152,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140587152,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1380929616","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1362538206","source":"dbSNP","start":140587163,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140587163,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140587164,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587164,"clinical_significance":[],"seq_region_name":"7","id":"rs1798816671"},{"clinical_significance":[],"id":"rs540329305","seq_region_name":"7","end":140587165,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140587165,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140587171,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587171,"clinical_significance":[],"seq_region_name":"7","id":"rs1798816879"},{"seq_region_name":"7","id":"rs999484454","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587181,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140587181},{"feature_type":"variation","strand":1,"end":140587182,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587182,"clinical_significance":[],"seq_region_name":"7","id":"rs562311606"},{"source":"dbSNP","start":140587184,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140587184,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs960155377","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140587189,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587189,"source":"dbSNP","seq_region_name":"7","id":"rs1798817336","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1173640154","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140587191,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587191},{"start":140587193,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140587193,"strand":1,"feature_type":"variation","id":"rs1798817522","seq_region_name":"7","clinical_significance":[]},{"end":140587203,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140587203,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1465449520"},{"seq_region_name":"7","id":"rs750253397","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587210,"source":"dbSNP","strand":1,"feature_type":"variation","end":140587210,"alleles":["G","T"]},{"alleles":["C","T"],"end":140587228,"strand":1,"feature_type":"variation","start":140587228,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs186186573","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587232,"feature_type":"variation","strand":1,"end":140587232,"alleles":["C","T"],"clinical_significance":[],"id":"rs1798817952","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587243,"source":"dbSNP","strand":1,"feature_type":"variation","end":140587243,"alleles":["C","G"],"seq_region_name":"7","id":"rs1798818057","clinical_significance":[]},{"start":140587248,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140587248,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs887403003","clinical_significance":[]},{"seq_region_name":"7","id":"rs1247639811","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140587252,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587252,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140587253,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587253,"source":"dbSNP","id":"rs529439195","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798818506","alleles":["G","A"],"end":140587259,"feature_type":"variation","strand":1,"source":"dbSNP","start":140587259,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140587260,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587260,"clinical_significance":[],"seq_region_name":"7","id":"rs1462838840"},{"start":140587264,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140587264,"strand":1,"feature_type":"variation","id":"rs1199979231","seq_region_name":"7","clinical_significance":[]},{"end":140587265,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140587265,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1798818956","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1798819058","seq_region_name":"7","source":"dbSNP","start":140587267,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140587267,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1340644941","clinical_significance":[],"strand":1,"feature_type":"variation","end":140587268,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587268,"source":"dbSNP"},{"id":"rs371700794","seq_region_name":"7","clinical_significance":[],"alleles":["A","G"],"end":140587270,"strand":1,"feature_type":"variation","start":140587270,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798819368","source":"dbSNP","start":140587270,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["ATTAT","AT"],"end":140587274,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1036086858","seq_region_name":"7","feature_type":"variation","strand":1,"end":140587271,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587271},{"clinical_significance":[],"seq_region_name":"7","id":"rs1225689795","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587274,"feature_type":"variation","strand":1,"end":140587274,"alleles":["T","C","G"]},{"clinical_significance":[],"id":"rs1798819698","seq_region_name":"7","end":140587279,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140587279,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140587280,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140587280,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585697684"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587281,"feature_type":"variation","strand":1,"end":140587281,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1341966118"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1316185466","feature_type":"variation","strand":1,"end":140587282,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587282},{"seq_region_name":"7","id":"rs1798820097","clinical_significance":[],"end":140587283,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140587283,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1246170644","feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140587285,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587285},{"clinical_significance":[],"id":"rs1798820478","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587288,"feature_type":"variation","strand":1,"end":140587288,"alleles":["C","T"]},{"source":"dbSNP","start":140587290,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140587290,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs973872041"},{"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140587300,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587300,"source":"dbSNP","id":"rs1798820692","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1331569409","seq_region_name":"7","feature_type":"variation","strand":1,"end":140587301,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587301},{"seq_region_name":"7","id":"rs758057874","clinical_significance":[],"alleles":["G","A"],"end":140587302,"strand":1,"feature_type":"variation","start":140587302,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140587303,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587303,"clinical_significance":[],"seq_region_name":"7","id":"rs1798821035"},{"id":"rs1585697758","seq_region_name":"7","clinical_significance":[],"start":140587308,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140587308,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798821221","source":"dbSNP","start":140587310,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140587310,"alleles":["A","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs2130649242","clinical_significance":[],"strand":1,"feature_type":"variation","end":140587310,"alleles":["A","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587310,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1798821321","clinical_significance":[],"alleles":["G","C"],"end":140587313,"strand":1,"feature_type":"variation","start":140587313,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["A","G"],"end":140587319,"feature_type":"variation","strand":1,"source":"dbSNP","start":140587319,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1372031269"},{"end":140587321,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140587321,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798821512","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140587322,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587322,"clinical_significance":[],"seq_region_name":"7","id":"rs1798821636"},{"seq_region_name":"7","id":"rs548194998","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140587323,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587323,"source":"dbSNP"},{"seq_region_name":"7","id":"rs997339142","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140587324,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587324,"source":"dbSNP"},{"source":"dbSNP","start":140587325,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140587325,"alleles":["T","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1029351280"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587327,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140587327,"clinical_significance":[],"id":"rs779730554","seq_region_name":"7"},{"start":140587328,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140587328,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","id":"rs951089995","seq_region_name":"7","clinical_significance":[]},{"id":"rs566776235","seq_region_name":"7","clinical_significance":[],"end":140587330,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140587330,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798822627","source":"dbSNP","start":140587331,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140587331,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs746492346","clinical_significance":[],"alleles":["C","G","T"],"end":140587334,"strand":1,"feature_type":"variation","start":140587334,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140587335,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587335,"clinical_significance":[],"seq_region_name":"7","id":"rs1798822992"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1212216727","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587337,"feature_type":"variation","strand":1,"end":140587338,"alleles":["GC","-"]},{"seq_region_name":"7","id":"rs1798823299","clinical_significance":[],"strand":1,"feature_type":"variation","end":140587340,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587340,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1022257196","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587347,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","G","T"],"end":140587347},{"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140587348,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587348,"source":"dbSNP","seq_region_name":"7","id":"rs1186886964","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130649364","alleles":["G","T"],"end":140587355,"feature_type":"variation","strand":1,"source":"dbSNP","start":140587355,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1289746892","seq_region_name":"7","clinical_significance":[],"end":140587359,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140587359,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1798824008","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140587368,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587368,"source":"dbSNP"},{"id":"rs1585697891","seq_region_name":"7","clinical_significance":[],"start":140587371,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140587371,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"alleles":["C","T"],"end":140587375,"strand":1,"feature_type":"variation","start":140587375,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs77936717","seq_region_name":"7","clinical_significance":[]},{"start":140587376,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140587376,"strand":1,"feature_type":"variation","id":"rs1184668401","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140587379,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587379,"source":"dbSNP","seq_region_name":"7","id":"rs1798825013","clinical_significance":[]},{"start":140587380,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140587380,"strand":1,"feature_type":"variation","id":"rs1194523992","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798825357","feature_type":"variation","strand":1,"end":140587381,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587381},{"source":"dbSNP","start":140587383,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140587383,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs141398085"},{"seq_region_name":"7","id":"rs112174422","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140587384,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587384,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587385,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140587385,"seq_region_name":"7","id":"rs961184782","clinical_significance":[]},{"end":140587389,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140587389,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1188847326"},{"clinical_significance":[],"id":"rs992326207","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140587391,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587391},{"feature_type":"variation","strand":1,"end":140587392,"alleles":["G","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587392,"clinical_significance":[],"seq_region_name":"7","id":"rs1039500239"},{"strand":1,"feature_type":"variation","end":140587396,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587396,"source":"dbSNP","seq_region_name":"7","id":"rs1798826323","clinical_significance":[]},{"alleles":["A","C"],"end":140587400,"feature_type":"variation","strand":1,"source":"dbSNP","start":140587400,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585697969"},{"start":140587401,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G","T"],"end":140587401,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs145638790","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140587402,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587402,"clinical_significance":[],"seq_region_name":"7","id":"rs1308521578"},{"clinical_significance":[],"id":"rs969630338","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587403,"feature_type":"variation","strand":1,"end":140587403,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs985006566","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140587407,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587407},{"seq_region_name":"7","id":"rs1798827069","clinical_significance":[],"alleles":["C","T"],"end":140587411,"strand":1,"feature_type":"variation","start":140587411,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140587414,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587414,"clinical_significance":[],"id":"rs1426374314","seq_region_name":"7"},{"seq_region_name":"7","id":"rs2130649525","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140587416,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587416,"source":"dbSNP"},{"clinical_significance":[],"id":"rs2130649539","seq_region_name":"7","alleles":["G","A"],"end":140587421,"feature_type":"variation","strand":1,"source":"dbSNP","start":140587421,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs556266944","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587422,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140587422},{"seq_region_name":"7","id":"rs1162960808","clinical_significance":[],"start":140587423,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140587423,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1043160263","clinical_significance":[],"strand":1,"feature_type":"variation","end":140587424,"alleles":["CC","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587423,"source":"dbSNP"},{"source":"dbSNP","start":140587426,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140587426,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs908889044"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1365553099","source":"dbSNP","start":140587428,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140587428,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140587429,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587429,"clinical_significance":[],"seq_region_name":"7","id":"rs1798827871"},{"start":140587433,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140587433,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1326848537","clinical_significance":[]},{"end":140587434,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140587434,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs998869898","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798828126","clinical_significance":[],"start":140587435,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140587435,"alleles":["A","C","T"],"strand":1,"feature_type":"variation"},{"alleles":["C","A","G"],"end":140587437,"feature_type":"variation","strand":1,"source":"dbSNP","start":140587437,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs574576421","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798828382","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587438,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140587438},{"end":140587443,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140587443,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798828496"},{"alleles":["C","A"],"end":140587445,"feature_type":"variation","strand":1,"source":"dbSNP","start":140587445,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798828605"},{"strand":1,"feature_type":"variation","end":140587449,"alleles":["CCCCC","CCCC"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587445,"source":"dbSNP","seq_region_name":"7","id":"rs1563160705","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1057451257","end":140587446,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140587446,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1798828960","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140587458,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587458,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140587460,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587460,"source":"dbSNP","seq_region_name":"7","id":"rs1798829072","clinical_significance":[]},{"end":140587461,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140587461,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798829236","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587462,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140587462,"seq_region_name":"7","id":"rs896061979","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140587464,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587464,"clinical_significance":[],"seq_region_name":"7","id":"rs867813018"},{"end":140587465,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140587465,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1036135557","clinical_significance":[]},{"id":"rs541836614","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140587472,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587472,"source":"dbSNP"},{"end":140587474,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","start":140587474,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs923030306","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140587476,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140587476,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1294675286"},{"end":140587479,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140587479,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1226070875"},{"seq_region_name":"7","id":"rs1261917709","clinical_significance":[],"strand":1,"feature_type":"variation","end":140587479,"alleles":["C","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587479,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1798830832","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587486,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140587486},{"end":140587489,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140587489,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1023118887"},{"id":"rs1283918294","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587492,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140587492},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585698236","alleles":["A","C"],"end":140587495,"feature_type":"variation","strand":1,"source":"dbSNP","start":140587495,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","A"],"end":140587499,"strand":1,"feature_type":"variation","start":140587499,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585698245","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs963556032","end":140587500,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140587500,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140587504,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587504,"clinical_significance":[],"seq_region_name":"7","id":"rs995633714"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798831919","feature_type":"variation","strand":1,"end":140587504,"alleles":["-","AAT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587505},{"seq_region_name":"7","id":"rs1798832018","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587506,"source":"dbSNP","strand":1,"feature_type":"variation","end":140587505,"alleles":["-","AGGAA"]},{"alleles":["G","A","C"],"end":140587508,"feature_type":"variation","strand":1,"source":"dbSNP","start":140587508,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1401456246"},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140587510,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587510,"source":"dbSNP","seq_region_name":"7","id":"rs1798832254","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587511,"source":"dbSNP","strand":1,"feature_type":"variation","end":140587511,"alleles":["T","C"],"seq_region_name":"7","id":"rs2130649811","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1387456785","alleles":["C","T"],"end":140587519,"feature_type":"variation","strand":1,"source":"dbSNP","start":140587519,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140587520,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587520,"source":"dbSNP","seq_region_name":"7","id":"rs933181071","clinical_significance":[]},{"clinical_significance":[],"id":"rs1050272279","seq_region_name":"7","end":140587524,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140587524,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130649844","end":140587527,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140587527,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140587530,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587530,"clinical_significance":[],"id":"rs1456824072","seq_region_name":"7"},{"seq_region_name":"7","id":"rs560086883","clinical_significance":[],"start":140587531,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140587531,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798832942","source":"dbSNP","start":140587537,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140587537,"alleles":["C","T"],"feature_type":"variation","strand":1},{"start":140587539,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140587539,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs545052085","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1283952873","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587540,"feature_type":"variation","strand":1,"end":140587540,"alleles":["G","C"]},{"id":"rs375224965","seq_region_name":"7","clinical_significance":[],"start":140587540,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140587553,"alleles":["GTGTGTGTGTGTGT","GTGTGTGTGTGT","GTGTGTGTGTGTGTGT","GTGTGTGTGTGTGTGTGT"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140587542,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587542,"source":"dbSNP","seq_region_name":"7","id":"rs1246428674","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798833605","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587546,"source":"dbSNP","strand":1,"feature_type":"variation","end":140587546,"alleles":["G","A","T"]},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140587548,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587548,"source":"dbSNP","seq_region_name":"7","id":"rs1011457466","clinical_significance":[]},{"start":140587549,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140587549,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798833817","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140587553,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587553,"clinical_significance":[],"id":"rs551804698","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs965249121","source":"dbSNP","start":140587556,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140587556,"alleles":["A","C","G"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["AT","-"],"end":140587557,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587556,"source":"dbSNP","seq_region_name":"7","id":"rs1798834160","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140587557,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587557,"clinical_significance":[],"seq_region_name":"7","id":"rs1482729041"},{"alleles":["G","A"],"end":140587560,"strand":1,"feature_type":"variation","start":140587560,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1206273024","clinical_significance":[]},{"seq_region_name":"7","id":"rs903882735","clinical_significance":[],"start":140587564,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140587564,"strand":1,"feature_type":"variation"},{"end":140587565,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140587565,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs999464505","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140587567,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140587567,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs546140518"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140587568,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587568,"source":"dbSNP","seq_region_name":"7","id":"rs960819983","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140587569,"alleles":["T","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587569,"source":"dbSNP","seq_region_name":"7","id":"rs1798834917","clinical_significance":[]},{"id":"rs1798835032","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140587583,"alleles":["CAGCAGC","CAGCAGCAGC"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587577,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140587579,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587579,"source":"dbSNP","id":"rs1342815085","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585698472","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587582,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140587582},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587586,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140587586,"clinical_significance":[],"seq_region_name":"7","id":"rs1798835370"},{"source":"dbSNP","start":140587589,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140587589,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1273991350"},{"end":140587592,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140587592,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs780720810","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs921067374","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587594,"feature_type":"variation","strand":1,"end":140587594,"alleles":["C","A"]},{"source":"dbSNP","start":140587596,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140587596,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs879440801"},{"clinical_significance":[],"id":"rs1406832938","seq_region_name":"7","end":140587597,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140587597,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1798836059","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140587600,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587600,"source":"dbSNP"},{"alleles":["C","T"],"end":140587602,"feature_type":"variation","strand":1,"source":"dbSNP","start":140587602,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798836181"},{"clinical_significance":[],"seq_region_name":"7","id":"rs969516012","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587604,"feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140587604},{"alleles":["TTT","TTTTT"],"end":140587606,"strand":1,"feature_type":"variation","start":140587604,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1271703739","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140587609,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140587609,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs748316499","seq_region_name":"7"},{"end":140587619,"alleles":["CAGACAGAC","CAGAC"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140587611,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs773886380"},{"source":"dbSNP","start":140587614,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140587614,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs201584656"},{"alleles":["A","G","T"],"end":140587616,"feature_type":"variation","strand":1,"source":"dbSNP","start":140587616,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs773627086"},{"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140587617,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587617,"source":"dbSNP","seq_region_name":"7","id":"rs1563160844","clinical_significance":[]},{"seq_region_name":"7","id":"rs138274867","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587618,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G","T"],"end":140587618},{"id":"rs762823379","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587619,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140587619},{"feature_type":"variation","strand":1,"end":140587621,"alleles":["C","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587621,"clinical_significance":[],"id":"rs1425117157","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs550379061","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587623,"feature_type":"variation","strand":1,"end":140587623,"alleles":["G","A","C"]},{"seq_region_name":"7","id":"rs1303469479","clinical_significance":[],"alleles":["A","T"],"end":140587624,"strand":1,"feature_type":"variation","start":140587624,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs2130650146","clinical_significance":[],"start":140587626,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140587626,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140587627,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587627,"clinical_significance":[],"id":"rs190989636","seq_region_name":"7"},{"seq_region_name":"7","id":"rs761393704","clinical_significance":[],"start":140587628,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140587628,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs767139017","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587629,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140587629},{"clinical_significance":[],"id":"rs750143274","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140587630,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587630},{"seq_region_name":"7","id":"rs142893936","clinical_significance":[],"start":140587631,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140587631,"alleles":["C","A","G","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs200641006","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587632,"source":"dbSNP","strand":1,"feature_type":"variation","end":140587632,"alleles":["A","G"]},{"alleles":["C","T"],"end":140587633,"strand":1,"feature_type":"variation","start":140587633,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs879945253","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587637,"feature_type":"variation","strand":1,"end":140587637,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs867507728"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587638,"feature_type":"variation","strand":1,"end":140587638,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs754319459"},{"clinical_significance":[],"id":"rs1468342058","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587639,"feature_type":"variation","strand":1,"end":140587639,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1489959077","source":"dbSNP","start":140587640,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140587640,"alleles":["T","C"],"feature_type":"variation","strand":1},{"start":140587645,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_region_variant","end":140587645,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1222458538","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs755446980","consequence_type":"splice_donor_5th_base_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587648,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140587648},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798839378","feature_type":"variation","strand":1,"end":140587649,"alleles":["T","C"],"consequence_type":"splice_donor_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587649},{"clinical_significance":[],"seq_region_name":"7","id":"rs1480690093","alleles":["A","T"],"end":140587651,"feature_type":"variation","strand":1,"source":"dbSNP","start":140587651,"consequence_type":"splice_donor_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs779363585","end":140587653,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140587653,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"alleles":["A","G"],"end":140587655,"strand":1,"feature_type":"variation","start":140587655,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs1798839676","clinical_significance":["uncertain significance"]},{"source":"dbSNP","start":140587656,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140587656,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1798839810","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1243168360","seq_region_name":"7","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587661,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140587661},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587662,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140587662,"clinical_significance":[],"id":"rs1211659361","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140587663,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587663,"clinical_significance":[],"seq_region_name":"7","id":"rs1440598306"},{"seq_region_name":"7","id":"rs748510783","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140587668,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140587668,"source":"dbSNP"},{"start":140587671,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["C","T"],"end":140587671,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs375197864","clinical_significance":["uncertain significance"]},{"seq_region_name":"7","id":"rs369401708","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140587672,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140587672},{"clinical_significance":[],"seq_region_name":"7","id":"rs1341294882","source":"dbSNP","start":140587678,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","end":140587678,"alleles":["C","T"],"feature_type":"variation","strand":1},{"alleles":["C","G"],"end":140587680,"strand":1,"feature_type":"variation","start":140587680,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs2130650312","clinical_significance":[]},{"id":"rs1386923354","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140587681,"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140587681,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140587682,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587682,"clinical_significance":[],"seq_region_name":"7","id":"rs747288299"},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140587686,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140587686,"seq_region_name":"7","id":"rs1164036058","clinical_significance":[]},{"alleles":["A","C"],"end":140587687,"feature_type":"variation","strand":1,"source":"dbSNP","start":140587687,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs566302408"},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140587689,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140587689,"seq_region_name":"7","id":"rs776608149","clinical_significance":["uncertain significance"]},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140587691,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140587691,"id":"rs948923920","seq_region_name":"7","clinical_significance":[]},{"id":"rs372846744","seq_region_name":"7","clinical_significance":[],"start":140587692,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140587692,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140587693,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587693,"clinical_significance":[],"seq_region_name":"7","id":"rs1798842206"},{"alleles":["C","A"],"end":140587700,"feature_type":"variation","strand":1,"source":"dbSNP","start":140587700,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798842317"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798842439","alleles":["C","T"],"end":140587702,"feature_type":"variation","strand":1,"source":"dbSNP","start":140587702,"consequence_type":"synonymous_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs146122731","clinical_significance":["uncertain significance"],"strand":1,"feature_type":"variation","end":140587704,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140587704,"source":"dbSNP"},{"end":140587711,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140587711,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs774327008"},{"strand":1,"feature_type":"variation","end":140587714,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140587714,"source":"dbSNP","id":"rs201968906","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140587715,"source":"dbSNP","strand":1,"feature_type":"variation","end":140587715,"alleles":["G","A"],"id":"rs1798843214","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs201039739","alleles":["C","A","T"],"end":140587716,"feature_type":"variation","strand":1,"source":"dbSNP","start":140587716,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs183962765","alleles":["G","A"],"end":140587717,"feature_type":"variation","strand":1,"source":"dbSNP","start":140587717,"consequence_type":"synonymous_variant","assembly_name":"GRCh38"},{"end":140587721,"alleles":["C","A","G"],"strand":1,"feature_type":"variation","start":140587721,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs1309717757","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140587722,"source":"dbSNP","strand":1,"feature_type":"variation","end":140587722,"alleles":["A","C","T"],"seq_region_name":"7","id":"rs886850370","clinical_significance":[]},{"end":140587723,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140587723,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","seq_region_name":"7","id":"rs1798844537","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1230743554","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140587725,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587725},{"clinical_significance":[],"id":"rs1206009726","seq_region_name":"7","end":140587729,"alleles":["CCACC","CC"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140587725,"consequence_type":"inframe_deletion","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1456919407","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140587726,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140587726},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140587727,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140587727,"source":"dbSNP","seq_region_name":"7","id":"rs1004395390","clinical_significance":["uncertain significance"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1275637490","end":140587728,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140587728,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140587729,"alleles":["C","T"],"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587729,"clinical_significance":[],"seq_region_name":"7","id":"rs1244557940"},{"seq_region_name":"7","id":"rs537684680","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140587730,"source":"dbSNP","strand":1,"feature_type":"variation","end":140587730,"alleles":["C","T"]},{"strand":1,"feature_type":"variation","end":140587733,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140587733,"source":"dbSNP","id":"rs1181013426","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs765871045","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140587734,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140587734,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1411659067","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140587735,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140587735},{"clinical_significance":[],"seq_region_name":"7","id":"rs377025611","end":140587738,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140587738,"consequence_type":"synonymous_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs2130650563","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140587742,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140587742,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798846204","alleles":["G","T"],"end":140587744,"feature_type":"variation","strand":1,"source":"dbSNP","start":140587744,"consequence_type":"synonymous_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140587745,"source":"dbSNP","strand":1,"feature_type":"variation","end":140587745,"alleles":["G","A"],"id":"rs1399717123","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587750,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140587750,"clinical_significance":[],"seq_region_name":"7","id":"rs1470324504"},{"alleles":["-","A"],"end":140587752,"strand":1,"feature_type":"variation","start":140587753,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"frameshift_variant","seq_region_name":"7","id":"rs761088808","clinical_significance":[]},{"seq_region_name":"7","id":"rs754576306","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140587753,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140587753},{"consequence_type":"frameshift_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587753,"feature_type":"variation","strand":1,"alleles":["C","-"],"end":140587753,"clinical_significance":[],"seq_region_name":"7","id":"rs1798847305"},{"start":140587754,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["A","C","G"],"end":140587754,"strand":1,"feature_type":"variation","id":"rs1447776429","seq_region_name":"7","clinical_significance":[]},{"start":140587755,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140587755,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs765835840","clinical_significance":[]},{"clinical_significance":[],"id":"rs1798848103","seq_region_name":"7","end":140587755,"alleles":["-","AGTCT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140587756,"consequence_type":"frameshift_variant","assembly_name":"GRCh38"},{"id":"rs766702133","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"frameshift_variant","start":140587757,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["-","CTTC"],"end":140587756},{"consequence_type":"stop_gained","assembly_name":"GRCh38","source":"dbSNP","start":140587757,"feature_type":"variation","strand":1,"end":140587757,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1798848536"},{"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140587758,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140587758,"id":"rs1204212532","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs776895682","end":140587760,"alleles":["AT","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140587759,"consequence_type":"frameshift_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140587760,"consequence_type":"frameshift_variant","assembly_name":"GRCh38","end":140587760,"alleles":["T","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798849150"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1360395874","alleles":["T","C"],"end":140587762,"feature_type":"variation","strand":1,"source":"dbSNP","start":140587762,"consequence_type":"synonymous_variant","assembly_name":"GRCh38"},{"id":"rs1019218499","seq_region_name":"7","clinical_significance":[],"start":140587764,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140587764,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"start":140587766,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140587766,"alleles":["A","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs187732883","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140587771,"source":"dbSNP","strand":1,"feature_type":"variation","end":140587771,"alleles":["A","G"],"seq_region_name":"7","id":"rs747217732","clinical_significance":[]},{"seq_region_name":"7","id":"rs1378446181","clinical_significance":[],"alleles":["T","C","G"],"end":140587772,"strand":1,"feature_type":"variation","start":140587772,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798850149","source":"dbSNP","start":140587773,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140587773,"alleles":["A","G"],"feature_type":"variation","strand":1},{"start":140587775,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["G","A"],"end":140587775,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130650712","clinical_significance":[]},{"consequence_type":"splice_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587780,"feature_type":"variation","strand":1,"end":140587780,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1203693425"},{"alleles":["G","A"],"end":140587784,"strand":1,"feature_type":"variation","start":140587784,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_region_variant","seq_region_name":"7","id":"rs1798850431","clinical_significance":[]},{"id":"rs1798850551","seq_region_name":"7","clinical_significance":[],"alleles":["G","T"],"end":140587790,"strand":1,"feature_type":"variation","start":140587790,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_polypyrimidine_tract_variant"},{"seq_region_name":"7","id":"rs1798850656","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"splice_polypyrimidine_tract_variant","start":140587791,"source":"dbSNP","strand":1,"feature_type":"variation","end":140587791,"alleles":["C","G"]},{"feature_type":"variation","strand":1,"end":140587796,"alleles":["T","A","C"],"consequence_type":"splice_polypyrimidine_tract_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587796,"clinical_significance":[],"id":"rs371340218","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587798,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140587798,"seq_region_name":"7","id":"rs6954743","clinical_significance":[]},{"source":"dbSNP","start":140587799,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140587799,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs745918940"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587801,"feature_type":"variation","strand":1,"end":140587801,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1798851149"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1242550255","source":"dbSNP","start":140587803,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140587808,"alleles":["AAAAAA","AAAAAAA"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1196302837","seq_region_name":"7","end":140587808,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140587808,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140587813,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140587813,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1476260264","seq_region_name":"7"},{"end":140587821,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140587821,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1184755898"},{"seq_region_name":"7","id":"rs377656523","clinical_significance":[],"alleles":["T","C"],"end":140587822,"strand":1,"feature_type":"variation","start":140587822,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140587831,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140587831,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs776405709"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587846,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140587846,"clinical_significance":[],"seq_region_name":"7","id":"rs1798851947"},{"strand":1,"feature_type":"variation","end":140587854,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587854,"source":"dbSNP","seq_region_name":"7","id":"rs1563161175","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140587857,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587857,"source":"dbSNP","seq_region_name":"7","id":"rs373710831","clinical_significance":[]},{"seq_region_name":"7","id":"rs1365797367","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140587859,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587859,"source":"dbSNP"},{"source":"dbSNP","start":140587861,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140587861,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1175487216","seq_region_name":"7"},{"source":"dbSNP","start":140587863,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140587863,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs772221091","seq_region_name":"7"},{"end":140587864,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140587864,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs554147791","seq_region_name":"7","clinical_significance":[]},{"end":140587867,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140587867,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798853225","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798853404","feature_type":"variation","strand":1,"end":140587872,"alleles":["AAATT","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587868},{"end":140587874,"alleles":["TTTT","TTT"],"strand":1,"feature_type":"variation","start":140587871,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798853588","clinical_significance":[]},{"source":"dbSNP","start":140587875,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140587875,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs775435752","seq_region_name":"7"},{"id":"rs969566578","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587878,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140587878},{"id":"rs1798854144","seq_region_name":"7","clinical_significance":[],"start":140587890,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140587890,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"alleles":["T","C"],"end":140587891,"feature_type":"variation","strand":1,"source":"dbSNP","start":140587891,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585699565"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1473507517","feature_type":"variation","strand":1,"end":140587897,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587897},{"seq_region_name":"7","id":"rs1158717064","clinical_significance":[],"start":140587898,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140587898,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1181156747","source":"dbSNP","start":140587899,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140587899,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1490467712","clinical_significance":[],"start":140587903,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140587903,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1798855205","clinical_significance":[],"start":140587908,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TTTTATTTTATTT","TTTTATTT"],"end":140587920,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798855397","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140587912,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587912},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587915,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140587915,"id":"rs934744056","seq_region_name":"7","clinical_significance":[]},{"id":"rs1798855766","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140587923,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587923,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587923,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TTTTTT","TTTTTTT"],"end":140587928,"seq_region_name":"7","id":"rs1798855945","clinical_significance":[]},{"clinical_significance":[],"id":"rs1798856050","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587926,"feature_type":"variation","strand":1,"end":140587926,"alleles":["T","G"]},{"clinical_significance":[],"id":"rs1219583385","seq_region_name":"7","feature_type":"variation","strand":1,"end":140587928,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587928},{"seq_region_name":"7","id":"rs2130650976","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587929,"source":"dbSNP","strand":1,"feature_type":"variation","end":140587929,"alleles":["G","C"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587934,"feature_type":"variation","strand":1,"alleles":["AAA","A"],"end":140587936,"clinical_significance":[],"seq_region_name":"7","id":"rs1321376124"},{"end":140587945,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140587945,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs572390298","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1006379604","clinical_significance":[],"strand":1,"feature_type":"variation","end":140587946,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587946,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1384224281","alleles":["G","A"],"end":140587947,"feature_type":"variation","strand":1,"source":"dbSNP","start":140587947,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1798856666","clinical_significance":[],"strand":1,"feature_type":"variation","end":140587951,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587951,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140587956,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587956,"clinical_significance":[],"seq_region_name":"7","id":"rs1016557433"},{"id":"rs2130651021","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587962,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140587962},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587963,"source":"dbSNP","strand":1,"feature_type":"variation","end":140587963,"alleles":["G","A"],"seq_region_name":"7","id":"rs6958659","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587964,"source":"dbSNP","strand":1,"feature_type":"variation","end":140587964,"alleles":["G","A"],"seq_region_name":"7","id":"rs917223721","clinical_significance":[]},{"end":140587968,"alleles":["C","A","G","T"],"strand":1,"feature_type":"variation","start":140587968,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs972689070","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs778254392","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140587969,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587969},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140587971,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587971,"clinical_significance":[],"seq_region_name":"7","id":"rs112391231"},{"clinical_significance":[],"id":"rs149427478","seq_region_name":"7","source":"dbSNP","start":140587972,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140587972,"alleles":["G","A"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140587974,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587974,"clinical_significance":[],"id":"rs985918223","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140587975,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587975,"clinical_significance":[],"seq_region_name":"7","id":"rs544048205"},{"seq_region_name":"7","id":"rs1409639957","clinical_significance":[],"end":140587976,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140587976,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587982,"source":"dbSNP","strand":1,"feature_type":"variation","end":140587982,"alleles":["C","T"],"seq_region_name":"7","id":"rs1158251048","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798858076","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587986,"feature_type":"variation","strand":1,"end":140587986,"alleles":["C","G"]},{"strand":1,"feature_type":"variation","end":140587995,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587995,"source":"dbSNP","seq_region_name":"7","id":"rs1798858173","clinical_significance":[]},{"clinical_significance":[],"id":"rs910284842","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140587996,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140587996},{"seq_region_name":"7","id":"rs1353138971","clinical_significance":[],"end":140587997,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140587997,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1798858576","clinical_significance":[],"end":140587998,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140587998,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140587999,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140587999,"seq_region_name":"7","id":"rs1798858668","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs947251169","end":140588000,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140588000,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140588012,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140588012,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs978557559","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588018,"feature_type":"variation","strand":1,"end":140588018,"alleles":["C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1798859127"},{"feature_type":"variation","strand":1,"end":140588020,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588020,"clinical_significance":[],"id":"rs1798859248","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1798859358","clinical_significance":[],"start":140588023,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140588023,"strand":1,"feature_type":"variation"},{"alleles":["C","T"],"end":140588025,"feature_type":"variation","strand":1,"source":"dbSNP","start":140588025,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1798859453","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588028,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140588028,"id":"rs1798859565","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798859686","source":"dbSNP","start":140588029,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140588029,"alleles":["G","T"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588030,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140588030,"id":"rs1585699819","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140588033,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588033,"clinical_significance":[],"seq_region_name":"7","id":"rs1798859890"},{"start":140588035,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140588035,"alleles":["A","G","T"],"strand":1,"feature_type":"variation","id":"rs6943180","seq_region_name":"7","clinical_significance":[]},{"id":"rs1798860186","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140588041,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588041,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588045,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140588045,"clinical_significance":[],"seq_region_name":"7","id":"rs1798860312"},{"clinical_significance":[],"id":"rs934603016","seq_region_name":"7","alleles":["T","C"],"end":140588051,"feature_type":"variation","strand":1,"source":"dbSNP","start":140588051,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1210657510","alleles":["A","T"],"end":140588056,"feature_type":"variation","strand":1,"source":"dbSNP","start":140588056,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1798860623","clinical_significance":[],"start":140588059,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140588059,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1798860731","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140588060,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588060,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1798860846","seq_region_name":"7","end":140588061,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140588061,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs568258560","clinical_significance":[],"end":140588063,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140588063,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140588064,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140588065,"alleles":["CC","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1267588209"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588065,"feature_type":"variation","strand":1,"end":140588065,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1195415959"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588068,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140588068,"clinical_significance":[],"seq_region_name":"7","id":"rs1798861336"},{"seq_region_name":"7","id":"rs535324167","clinical_significance":[],"start":140588069,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140588069,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140588075,"alleles":["T","TT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588075,"clinical_significance":[],"id":"rs1798861543","seq_region_name":"7"},{"seq_region_name":"7","id":"rs6958806","clinical_significance":[],"start":140588077,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140588077,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1798861805","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588078,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140588078},{"seq_region_name":"7","id":"rs1798861908","clinical_significance":[],"start":140588085,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140588085,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140588087,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140588087,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1181928651"},{"seq_region_name":"7","id":"rs766193978","clinical_significance":[],"start":140588089,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140588089,"alleles":["T","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798862239","source":"dbSNP","start":140588091,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140588092,"alleles":["AG","-"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1386601107","clinical_significance":[],"start":140588091,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AGTAGAGACAA","A"],"end":140588101,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140588092,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588092,"source":"dbSNP","seq_region_name":"7","id":"rs1366438198","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140588093,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588093,"clinical_significance":[],"seq_region_name":"7","id":"rs1320876414"},{"feature_type":"variation","strand":1,"end":140588103,"alleles":["AGAGACAAAG","AG"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588094,"clinical_significance":[],"seq_region_name":"7","id":"rs1798862624"},{"seq_region_name":"7","id":"rs1798862735","clinical_significance":[],"start":140588095,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140588095,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"start":140588101,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140588101,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1436635767","clinical_significance":[]},{"source":"dbSNP","start":140588103,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140588103,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1798862941","seq_region_name":"7"},{"seq_region_name":"7","id":"rs2130651380","clinical_significance":[],"alleles":["T","C"],"end":140588110,"strand":1,"feature_type":"variation","start":140588110,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs751167190","clinical_significance":[],"start":140588111,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140588111,"strand":1,"feature_type":"variation"},{"start":140588112,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140588112,"strand":1,"feature_type":"variation","id":"rs1385738370","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1365081716","source":"dbSNP","start":140588124,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140588124,"feature_type":"variation","strand":1},{"start":140588130,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140588130,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1470220891","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140588131,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588131,"clinical_significance":[],"seq_region_name":"7","id":"rs1798863418"},{"clinical_significance":[],"id":"rs541985007","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588134,"feature_type":"variation","strand":1,"end":140588134,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1173670368","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588135,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140588135},{"id":"rs1432444092","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588138,"source":"dbSNP","strand":1,"feature_type":"variation","end":140588138,"alleles":["T","C"]},{"start":140588139,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140588139,"strand":1,"feature_type":"variation","id":"rs1798863857","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140588141,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140588141,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798863957"},{"end":140588142,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140588142,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1019330696","clinical_significance":[]},{"alleles":["A","G"],"end":140588145,"strand":1,"feature_type":"variation","start":140588145,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1756258697","clinical_significance":[]},{"clinical_significance":[],"id":"rs2130651465","seq_region_name":"7","source":"dbSNP","start":140588146,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140588146,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588147,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140588147,"id":"rs1585700057","seq_region_name":"7","clinical_significance":[]},{"start":140588152,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140588152,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798864261","clinical_significance":[]},{"alleles":["T","C"],"end":140588153,"feature_type":"variation","strand":1,"source":"dbSNP","start":140588153,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs370209031"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588156,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140588156,"clinical_significance":[],"seq_region_name":"7","id":"rs1798864472"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798864578","source":"dbSNP","start":140588158,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140588158,"alleles":["G","A"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140588159,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140588159,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1798864680","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1585700080","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588165,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140588165},{"seq_region_name":"7","id":"rs996467414","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140588166,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588166,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140588170,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588170,"clinical_significance":[],"id":"rs905267730","seq_region_name":"7"},{"alleles":["G","A","C"],"end":140588174,"strand":1,"feature_type":"variation","start":140588174,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1204419900","clinical_significance":[]},{"clinical_significance":[],"id":"rs560186497","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140588175,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588175},{"source":"dbSNP","start":140588176,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140588176,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1328436762"},{"start":140588177,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140588177,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1232966755","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140588179,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588179,"source":"dbSNP","seq_region_name":"7","id":"rs1798865561","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs34595342","feature_type":"variation","strand":1,"end":140588181,"alleles":["GGG","GGGG"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588179},{"source":"dbSNP","start":140588181,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140588181,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798865764"},{"id":"rs1798865862","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140588185,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588185,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798865957","source":"dbSNP","start":140588186,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140588186,"alleles":["T","C"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140588188,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140588188,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1016446089"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1369470396","alleles":["A","C","G"],"end":140588189,"feature_type":"variation","strand":1,"source":"dbSNP","start":140588189,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","T"],"end":140588190,"strand":1,"feature_type":"variation","start":140588190,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798866233","clinical_significance":[]},{"seq_region_name":"7","id":"rs1386235531","clinical_significance":[],"end":140588191,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140588191,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1307770480","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588194,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140588194},{"seq_region_name":"7","id":"rs754642520","clinical_significance":[],"start":140588197,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140588197,"strand":1,"feature_type":"variation"},{"id":"rs796882717","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140588198,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588198,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140588199,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588199,"clinical_significance":[],"seq_region_name":"7","id":"rs2130651609"},{"end":140588202,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140588202,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1362627237","clinical_significance":[]},{"alleles":["G","C"],"end":140588203,"feature_type":"variation","strand":1,"source":"dbSNP","start":140588203,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs897963409"},{"alleles":["C","T"],"end":140588211,"strand":1,"feature_type":"variation","start":140588211,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798866970","clinical_significance":[]},{"seq_region_name":"7","id":"rs79694613","clinical_significance":[],"start":140588216,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140588216,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140588217,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140588218,"alleles":["TT","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1396156954"},{"end":140588220,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140588220,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1404252431"},{"source":"dbSNP","start":140588222,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140588222,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1301085881"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1267810780","end":140588223,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140588223,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs752219480","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588226,"feature_type":"variation","strand":1,"end":140588226,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798867755","feature_type":"variation","strand":1,"end":140588228,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588228},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588229,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140588229,"clinical_significance":[],"id":"rs879170234","seq_region_name":"7"},{"alleles":["T","-"],"end":140588230,"strand":1,"feature_type":"variation","start":140588230,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1170276622","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798868102","source":"dbSNP","start":140588232,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140588232,"alleles":["T","C"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["AAAA","AAAAA"],"end":140588237,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588234,"source":"dbSNP","seq_region_name":"7","id":"rs1447842103","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798868335","clinical_significance":[],"strand":1,"feature_type":"variation","end":140588235,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588235,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs539734014","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588238,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140588238},{"clinical_significance":[],"id":"rs144153268","seq_region_name":"7","alleles":["C","T"],"end":140588239,"feature_type":"variation","strand":1,"source":"dbSNP","start":140588239,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1425692710","end":140588240,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140588240,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140588241,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140588241,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1254674344"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130651733","feature_type":"variation","strand":1,"alleles":["T","-"],"end":140588242,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588242},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588243,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140588243,"id":"rs183068424","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798869030","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588248,"source":"dbSNP","strand":1,"feature_type":"variation","end":140588248,"alleles":["A","C","T"]},{"clinical_significance":[],"id":"rs1563161461","seq_region_name":"7","feature_type":"variation","strand":1,"end":140588251,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588251},{"end":140588258,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140588258,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1271139310","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588264,"source":"dbSNP","strand":1,"feature_type":"variation","end":140588264,"alleles":["T","C"],"seq_region_name":"7","id":"rs1798869435","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588266,"source":"dbSNP","strand":1,"feature_type":"variation","end":140588266,"alleles":["T","C"],"seq_region_name":"7","id":"rs1488102803","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798869624","clinical_significance":[],"alleles":["A","G"],"end":140588273,"strand":1,"feature_type":"variation","start":140588273,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140588275,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140588275,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798869742","clinical_significance":[]},{"alleles":["T","C"],"end":140588276,"strand":1,"feature_type":"variation","start":140588276,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798869844","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140588280,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588280,"source":"dbSNP","seq_region_name":"7","id":"rs573108565","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798870092","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588282,"source":"dbSNP","strand":1,"feature_type":"variation","end":140588282,"alleles":["C","G","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588283,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140588283,"seq_region_name":"7","id":"rs1017342584","clinical_significance":[]},{"seq_region_name":"7","id":"rs968437156","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140588287,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588287,"source":"dbSNP"},{"end":140588290,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140588290,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798870323"},{"alleles":["G","T"],"end":140588296,"feature_type":"variation","strand":1,"source":"dbSNP","start":140588296,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs978447764"},{"start":140588297,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140588307,"alleles":["AAAATAATAAA","AAA"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1244881651","clinical_significance":[]},{"end":140588300,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140588300,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798870663"},{"clinical_significance":[],"id":"rs1798870779","seq_region_name":"7","end":140588303,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140588303,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs147355141","seq_region_name":"7","source":"dbSNP","start":140588307,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C","G"],"end":140588307,"feature_type":"variation","strand":1},{"end":140588310,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140588310,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1395334205","clinical_significance":[]},{"id":"rs535262304","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140588311,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588311,"source":"dbSNP"},{"alleles":["G","A"],"end":140588314,"feature_type":"variation","strand":1,"source":"dbSNP","start":140588314,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798871309"},{"end":140588316,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140588316,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798871408"},{"seq_region_name":"7","id":"rs779432176","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588320,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140588320},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588328,"source":"dbSNP","strand":1,"feature_type":"variation","end":140588328,"alleles":["T","C"],"seq_region_name":"7","id":"rs1798871635","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798871736","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588330,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140588330},{"strand":1,"feature_type":"variation","end":140588347,"alleles":["AACTTTGTAAACAAAC","AAC"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588332,"source":"dbSNP","seq_region_name":"7","id":"rs1309585688","clinical_significance":[]},{"end":140588334,"alleles":["C","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140588334,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798871982"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1427633008","source":"dbSNP","start":140588335,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140588335,"alleles":["T","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1370169018","clinical_significance":[],"alleles":["G","A","T"],"end":140588338,"strand":1,"feature_type":"variation","start":140588338,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140588348,"alleles":["AAACAAACA","AAACA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588340,"clinical_significance":[],"seq_region_name":"7","id":"rs1798872336"},{"clinical_significance":[],"seq_region_name":"7","id":"rs746020331","feature_type":"variation","strand":1,"alleles":["T","A"],"end":140588349,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588349},{"alleles":["G","C","T"],"end":140588351,"feature_type":"variation","strand":1,"source":"dbSNP","start":140588351,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1164113389","seq_region_name":"7"},{"end":140588352,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140588352,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798872693","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs139553440","alleles":["C","A","T"],"end":140588353,"feature_type":"variation","strand":1,"source":"dbSNP","start":140588353,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["G","A"],"end":140588354,"feature_type":"variation","strand":1,"source":"dbSNP","start":140588354,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs78177877"},{"clinical_significance":[],"id":"rs2130651975","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140588364,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588364},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798873106","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588369,"feature_type":"variation","strand":1,"alleles":["GGGGG","GGGG"],"end":140588373},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140588370,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588370,"source":"dbSNP","seq_region_name":"7","id":"rs1798873226","clinical_significance":[]},{"start":140588371,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C"],"end":140588371,"strand":1,"feature_type":"variation","id":"rs908002911","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588374,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140588374,"seq_region_name":"7","id":"rs1254656662","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs917139376","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140588375,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588375},{"feature_type":"variation","strand":1,"end":140588376,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588376,"clinical_significance":[],"seq_region_name":"7","id":"rs1798873701"},{"end":140588377,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140588377,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs539486497"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1045083578","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588387,"feature_type":"variation","strand":1,"end":140588387,"alleles":["C","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588395,"source":"dbSNP","strand":1,"feature_type":"variation","end":140588395,"alleles":["T","G"],"id":"rs1292967398","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["ATAGACA","A"],"end":140588402,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588396,"source":"dbSNP","seq_region_name":"7","id":"rs1210004503","clinical_significance":[]},{"seq_region_name":"7","id":"rs1358053982","clinical_significance":[],"start":140588401,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G","T"],"end":140588401,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588404,"source":"dbSNP","strand":1,"feature_type":"variation","end":140588404,"alleles":["G","A","T"],"seq_region_name":"7","id":"rs1263120600","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140588405,"alleles":["G","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588405,"clinical_significance":[],"seq_region_name":"7","id":"rs1351008378"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1290197830","end":140588406,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140588406,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs2130652064","clinical_significance":[],"end":140588408,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140588408,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs944880018","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140588410,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588410,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588411,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140588411,"clinical_significance":[],"id":"rs1349575764","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798874975","source":"dbSNP","start":140588414,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140588414,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1798875080","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588418,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140588418},{"seq_region_name":"7","id":"rs1323979865","clinical_significance":[],"start":140588422,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140588422,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798875312","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588428,"feature_type":"variation","strand":1,"end":140588428,"alleles":["T","A"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588429,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140588429,"clinical_significance":[],"id":"rs1798875423","seq_region_name":"7"},{"id":"rs1798875540","seq_region_name":"7","clinical_significance":[],"start":140588433,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140588433,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588436,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140588436,"seq_region_name":"7","id":"rs905152671","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798875765","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588437,"source":"dbSNP","strand":1,"feature_type":"variation","end":140588437,"alleles":["G","T"]},{"id":"rs1388898402","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140588438,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588438,"source":"dbSNP"},{"end":140588444,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140588444,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs900922629","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","A"],"end":140588446,"strand":1,"feature_type":"variation","start":140588446,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798876122","clinical_significance":[]},{"end":140588447,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140588447,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs942103778","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130652140","end":140588452,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140588452,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs2130652149","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140588454,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588454,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1457892620","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140588455,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588455},{"strand":1,"feature_type":"variation","end":140588456,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588456,"source":"dbSNP","seq_region_name":"7","id":"rs1414832357","clinical_significance":[]},{"end":140588460,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140588460,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798876604"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798876705","feature_type":"variation","strand":1,"end":140588462,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588462},{"seq_region_name":"7","id":"rs558100592","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588465,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140588465},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588471,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140588471,"clinical_significance":[],"seq_region_name":"7","id":"rs1585700855"},{"start":140588473,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140588473,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798877017","clinical_significance":[]},{"clinical_significance":[],"id":"rs576832516","seq_region_name":"7","feature_type":"variation","strand":1,"end":140588474,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588474},{"clinical_significance":[],"seq_region_name":"7","id":"rs898014606","source":"dbSNP","start":140588478,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140588478,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1269990697","feature_type":"variation","strand":1,"end":140588479,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588479},{"clinical_significance":[],"seq_region_name":"7","id":"rs544085108","source":"dbSNP","start":140588490,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140588490,"alleles":["G","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs994055618","clinical_significance":[],"start":140588494,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140588494,"strand":1,"feature_type":"variation"},{"id":"rs775627585","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140588497,"alleles":["G","A","C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588497,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1798877843","clinical_significance":[],"alleles":["A","C"],"end":140588501,"strand":1,"feature_type":"variation","start":140588501,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1798877977","clinical_significance":[],"start":140588509,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140588509,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1798878102","seq_region_name":"7","source":"dbSNP","start":140588512,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140588512,"alleles":["T","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1032012447","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140588513,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588513},{"seq_region_name":"7","id":"rs187338378","clinical_significance":[],"end":140588515,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140588515,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140588515,"alleles":["T","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140588515,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798878484"},{"source":"dbSNP","start":140588516,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140588516,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798878592"},{"end":140588517,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140588517,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798878689","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798878787","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140588521,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588521},{"seq_region_name":"7","id":"rs1563161619","clinical_significance":[],"start":140588522,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140588522,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["AGTCCCTGACTGTCTTATTACAGTATAGACAGTCCCTGACTGT","AGTCCCTGACTGTCTTATTACAGTATAGACAGTCCCTGACTGTCTTATTACAGTATAGACAGTCCCTGACTGT"],"end":140588564,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588522,"source":"dbSNP","seq_region_name":"7","id":"rs1287915963","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798879079","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588523,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140588523},{"seq_region_name":"7","id":"rs1329319593","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140588524,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588524,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1585700961","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140588527,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588527,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798879463","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588528,"feature_type":"variation","strand":1,"end":140588528,"alleles":["T","C"]},{"clinical_significance":[],"id":"rs1269481769","seq_region_name":"7","source":"dbSNP","start":140588531,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140588531,"feature_type":"variation","strand":1},{"id":"rs1798879671","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588532,"source":"dbSNP","strand":1,"feature_type":"variation","end":140588532,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1798879785","clinical_significance":[],"start":140588535,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140588535,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798879885","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140588537,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588537},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588538,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140588538,"clinical_significance":[],"seq_region_name":"7","id":"rs1226435394"},{"alleles":["C","T"],"end":140588542,"strand":1,"feature_type":"variation","start":140588542,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs574329614","clinical_significance":[]},{"clinical_significance":[],"id":"rs1798880402","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140588543,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588543},{"seq_region_name":"7","id":"rs1007265900","clinical_significance":[],"end":140588547,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140588547,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140588548,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140588548,"alleles":["A","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1017231751"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1329553372","source":"dbSNP","start":140588551,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140588551,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798880898","end":140588552,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140588552,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140588559,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588559,"source":"dbSNP","id":"rs1235418511","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798881187","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140588561,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588561,"source":"dbSNP"},{"start":140588568,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140588568,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","id":"rs968325649","seq_region_name":"7","clinical_significance":[]},{"end":140588571,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140588571,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs999918936"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1014092205","source":"dbSNP","start":140588579,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140588579,"alleles":["C","T"],"feature_type":"variation","strand":1},{"end":140588582,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140588582,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798881717","clinical_significance":[]},{"seq_region_name":"7","id":"rs75395698","clinical_significance":[],"end":140588589,"alleles":["C","A","G","T"],"strand":1,"feature_type":"variation","start":140588589,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588590,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140588590,"id":"rs1457138335","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1205117621","clinical_significance":[],"start":140588591,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140588591,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1253021247","clinical_significance":[],"end":140588593,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140588593,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588598,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140588598,"seq_region_name":"7","id":"rs774320352","clinical_significance":[]},{"clinical_significance":[],"id":"rs35490720","seq_region_name":"7","alleles":["TTTTT","TTTTTT"],"end":140588604,"feature_type":"variation","strand":1,"source":"dbSNP","start":140588600,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1477277695","end":140588606,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140588606,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140588608,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140588608,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798882770","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798882897","clinical_significance":[],"end":140588609,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140588609,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798882995","feature_type":"variation","strand":1,"end":140588611,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588611},{"clinical_significance":[],"seq_region_name":"7","id":"rs955926238","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588621,"feature_type":"variation","strand":1,"end":140588621,"alleles":["C","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588622,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140588622,"clinical_significance":[],"seq_region_name":"7","id":"rs1465076129"},{"clinical_significance":[],"seq_region_name":"7","id":"rs970114305","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588622,"feature_type":"variation","strand":1,"alleles":["GGGG","GGG"],"end":140588625},{"seq_region_name":"7","id":"rs370187516","clinical_significance":[],"start":140588625,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140588625,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"id":"rs993061717","seq_region_name":"7","clinical_significance":[],"alleles":["G","T"],"end":140588635,"strand":1,"feature_type":"variation","start":140588635,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140588636,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588636,"source":"dbSNP","id":"rs1798883702","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140588637,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140588637,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1203853552","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1249289811","feature_type":"variation","strand":1,"end":140588639,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588639},{"clinical_significance":[],"seq_region_name":"7","id":"rs980202681","source":"dbSNP","start":140588640,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140588640,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1271040373","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140588647,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588647},{"seq_region_name":"7","id":"rs917210080","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140588648,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588648,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798884414","end":140588649,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140588649,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1279322722","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140588656,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588656,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1486436982","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588667,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140588667},{"clinical_significance":[],"seq_region_name":"7","id":"rs920579423","source":"dbSNP","start":140588671,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140588671,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs2130652552","clinical_significance":[],"alleles":["C","T"],"end":140588678,"strand":1,"feature_type":"variation","start":140588678,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140588680,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588680,"clinical_significance":[],"id":"rs1274043067","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798885028","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588681,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140588681},{"alleles":["C","A"],"end":140588682,"strand":1,"feature_type":"variation","start":140588682,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs952150271","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1229353503","source":"dbSNP","start":140588684,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140588684,"feature_type":"variation","strand":1},{"alleles":["C","T"],"end":140588690,"strand":1,"feature_type":"variation","start":140588690,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs970380087","clinical_significance":[]},{"start":140588691,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140588691,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1295455826","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798885640","clinical_significance":[],"strand":1,"feature_type":"variation","end":140588696,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588696,"source":"dbSNP"},{"source":"dbSNP","start":140588701,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140588701,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1423657958","seq_region_name":"7"},{"end":140588702,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140588702,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1171669682"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1375293491","feature_type":"variation","strand":1,"end":140588703,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588703},{"clinical_significance":[],"seq_region_name":"7","id":"rs1434526105","source":"dbSNP","start":140588710,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140588710,"alleles":["G","A"],"feature_type":"variation","strand":1},{"start":140588711,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140588711,"alleles":["G","T"],"strand":1,"feature_type":"variation","id":"rs1360238421","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1427843688","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588712,"feature_type":"variation","strand":1,"end":140588712,"alleles":["T","C","G"]},{"start":140588714,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140588714,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs983682331","clinical_significance":[]},{"alleles":["A","T"],"end":140588716,"strand":1,"feature_type":"variation","start":140588716,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798886236","clinical_significance":[]},{"seq_region_name":"7","id":"rs1413267259","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588717,"source":"dbSNP","strand":1,"feature_type":"variation","end":140588717,"alleles":["G","A"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588719,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140588719,"clinical_significance":[],"seq_region_name":"7","id":"rs1798886437"},{"clinical_significance":[],"seq_region_name":"7","id":"rs979983826","feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140588720,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588720},{"feature_type":"variation","strand":1,"end":140588722,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588722,"clinical_significance":[],"seq_region_name":"7","id":"rs1416849577"},{"clinical_significance":[],"seq_region_name":"7","id":"rs926626220","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140588723,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588723},{"source":"dbSNP","start":140588731,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140588731,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798886953"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798887047","alleles":["A","C"],"end":140588734,"feature_type":"variation","strand":1,"source":"dbSNP","start":140588734,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588739,"feature_type":"variation","strand":1,"end":140588739,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs941987781"},{"clinical_significance":[],"seq_region_name":"7","id":"rs560024576","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140588743,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588743},{"clinical_significance":[],"id":"rs1798887370","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140588747,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588747},{"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140588751,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588751,"clinical_significance":[],"seq_region_name":"7","id":"rs527346219"},{"end":140588752,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140588752,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798887752","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588753,"source":"dbSNP","strand":1,"feature_type":"variation","end":140588753,"alleles":["A","C"],"seq_region_name":"7","id":"rs1011906497","clinical_significance":[]},{"start":140588754,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140588754,"alleles":["C","A"],"strand":1,"feature_type":"variation","id":"rs1585701478","seq_region_name":"7","clinical_significance":[]},{"start":140588755,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140588755,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1237555672","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588755,"feature_type":"variation","strand":1,"alleles":["TTTTTTT","TTTTTT","TTTTTTTT"],"end":140588761,"clinical_significance":[],"seq_region_name":"7","id":"rs1214946926"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588756,"feature_type":"variation","strand":1,"end":140588756,"alleles":["T","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1212078930"},{"clinical_significance":[],"id":"rs929526147","seq_region_name":"7","source":"dbSNP","start":140588758,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140588758,"alleles":["T","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1279292732","source":"dbSNP","start":140588759,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140588759,"alleles":["T","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1205656231","clinical_significance":[],"alleles":["T","G"],"end":140588760,"strand":1,"feature_type":"variation","start":140588760,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1611784","seq_region_name":"7","feature_type":"variation","strand":1,"end":140588761,"alleles":["T","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588761},{"seq_region_name":"7","id":"rs564062982","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140588762,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588762,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1798889566","seq_region_name":"7","feature_type":"variation","strand":1,"end":140588763,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588763},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588765,"feature_type":"variation","strand":1,"alleles":["A","C","T"],"end":140588765,"clinical_significance":[],"seq_region_name":"7","id":"rs902814541"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798889828","source":"dbSNP","start":140588765,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140588765,"alleles":["A","-"],"feature_type":"variation","strand":1},{"end":140588766,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140588766,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1222177509","seq_region_name":"7","clinical_significance":[]},{"end":140588766,"alleles":["-","AT"],"strand":1,"feature_type":"variation","start":140588767,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1798890060","seq_region_name":"7","clinical_significance":[]},{"id":"rs1280380108","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588767,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140588767},{"id":"rs34456581","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588767,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TTTTTTTTTTTTTTTTT","TTTTTTTTTT","TTTTTTTTTTTTT","TTTTTTTTTTTTTT","TTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT"],"end":140588783},{"end":140588769,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140588769,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1349508800"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588771,"feature_type":"variation","strand":1,"end":140588771,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1798891242"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588772,"feature_type":"variation","strand":1,"end":140588772,"alleles":["T","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1798891363"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588773,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140588773,"seq_region_name":"7","id":"rs1585701664","clinical_significance":[]},{"id":"rs1585701676","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140588782,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588782,"source":"dbSNP"},{"seq_region_name":"7","id":"rs79705527","clinical_significance":[],"start":140588783,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140588783,"strand":1,"feature_type":"variation"},{"alleles":["TG","-"],"end":140588784,"strand":1,"feature_type":"variation","start":140588783,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1554475148","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1798891983","seq_region_name":"7","source":"dbSNP","start":140588784,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140588783,"alleles":["-","TTTA"],"feature_type":"variation","strand":1},{"id":"rs77927282","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140588784,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588784,"source":"dbSNP"},{"source":"dbSNP","start":140588784,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","-"],"end":140588784,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798892212"},{"seq_region_name":"7","id":"rs2130652917","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588785,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140588785},{"source":"dbSNP","start":140588786,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140588785,"alleles":["-","TTTT"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798892321"},{"seq_region_name":"7","id":"rs1585701714","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588787,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140588787},{"clinical_significance":[],"seq_region_name":"7","id":"rs115074993","alleles":["C","G","T"],"end":140588788,"feature_type":"variation","strand":1,"source":"dbSNP","start":140588788,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1798892697","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["-","TTTTT"],"end":140588788,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588789,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588789,"source":"dbSNP","strand":1,"feature_type":"variation","end":140588789,"alleles":["C","G"],"seq_region_name":"7","id":"rs866433439","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798892906","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588791,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140588791},{"clinical_significance":[],"id":"rs1585701749","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588795,"feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140588795},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798893132","alleles":["G","A"],"end":140588799,"feature_type":"variation","strand":1,"source":"dbSNP","start":140588799,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs80176273","source":"dbSNP","start":140588800,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140588800,"alleles":["T","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs904153688","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140588804,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588804},{"alleles":["A","G"],"end":140588807,"strand":1,"feature_type":"variation","start":140588807,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1798893493","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140588810,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140588810,"alleles":["T","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798893616"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140588811,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588811,"clinical_significance":[],"seq_region_name":"7","id":"rs1000269742"},{"seq_region_name":"7","id":"rs1483951614","clinical_significance":[],"strand":1,"feature_type":"variation","end":140588813,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588813,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1052827402","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140588814,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588814,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs891707943","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588817,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140588817},{"start":140588823,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140588823,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1322573637","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588824,"source":"dbSNP","strand":1,"feature_type":"variation","end":140588824,"alleles":["C","A","T"],"seq_region_name":"7","id":"rs1007777787","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588826,"source":"dbSNP","strand":1,"feature_type":"variation","end":140588826,"alleles":["T","C"],"seq_region_name":"7","id":"rs998578586","clinical_significance":[]},{"source":"dbSNP","start":140588827,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140588827,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1264351921","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588828,"source":"dbSNP","strand":1,"feature_type":"variation","end":140588828,"alleles":["T","C"],"seq_region_name":"7","id":"rs1039237928","clinical_significance":[]},{"source":"dbSNP","start":140588829,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140588829,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798894650"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588832,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140588832,"seq_region_name":"7","id":"rs1798894772","clinical_significance":[]},{"clinical_significance":[],"id":"rs904219081","seq_region_name":"7","alleles":["T","C"],"end":140588835,"feature_type":"variation","strand":1,"source":"dbSNP","start":140588835,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1798895025","clinical_significance":[],"end":140588843,"alleles":["AA","A"],"strand":1,"feature_type":"variation","start":140588842,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140588845,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140588845,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs377594805"},{"alleles":["G","A"],"end":140588846,"feature_type":"variation","strand":1,"source":"dbSNP","start":140588846,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs531511666"},{"end":140588854,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140588854,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798895363"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588860,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140588860,"seq_region_name":"7","id":"rs1395750896","clinical_significance":[]},{"alleles":["C","A"],"end":140588862,"feature_type":"variation","strand":1,"source":"dbSNP","start":140588862,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798895587"},{"seq_region_name":"7","id":"rs1798895692","clinical_significance":[],"end":140588863,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140588863,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140588867,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588867,"source":"dbSNP","seq_region_name":"7","id":"rs1436672897","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798895939","source":"dbSNP","start":140588868,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140588868,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1798896049","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588870,"feature_type":"variation","strand":1,"end":140588870,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1798896138","clinical_significance":[],"alleles":["GGAGCTGGGA","GGA"],"end":140588879,"strand":1,"feature_type":"variation","start":140588870,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1166261591","feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140588871,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588871},{"seq_region_name":"7","id":"rs1403155010","clinical_significance":[],"start":140588872,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140588872,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588873,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140588873,"id":"rs1417073980","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588875,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140588875,"seq_region_name":"7","id":"rs549706254","clinical_significance":[]},{"seq_region_name":"7","id":"rs1174140997","clinical_significance":[],"end":140588876,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140588876,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1159729043","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140588879,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588879,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588885,"feature_type":"variation","strand":1,"end":140588885,"alleles":["T","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1798896886"},{"id":"rs955979047","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140588886,"strand":1,"feature_type":"variation","start":140588886,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588888,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140588888,"clinical_significance":[],"id":"rs1798897093","seq_region_name":"7"},{"end":140588890,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140588890,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1249281575","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140588892,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588892,"source":"dbSNP","id":"rs1798897303","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1013963657","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588893,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140588893},{"source":"dbSNP","start":140588894,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140588894,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1176437246"},{"strand":1,"feature_type":"variation","end":140588899,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588899,"source":"dbSNP","id":"rs1488910590","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588901,"source":"dbSNP","strand":1,"feature_type":"variation","end":140588901,"alleles":["T","C"],"seq_region_name":"7","id":"rs1248735476","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140588903,"alleles":["T","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588903,"clinical_significance":[],"seq_region_name":"7","id":"rs1798897930"},{"end":140588904,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140588904,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798898124","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588904,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GG","G"],"end":140588905,"seq_region_name":"7","id":"rs2130653270","clinical_significance":[]},{"seq_region_name":"7","id":"rs1024564973","clinical_significance":[],"end":140588905,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140588905,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588910,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140588910,"clinical_significance":[],"seq_region_name":"7","id":"rs772983284"},{"clinical_significance":[],"id":"rs1431134668","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140588914,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588914},{"strand":1,"feature_type":"variation","end":140588915,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588915,"source":"dbSNP","seq_region_name":"7","id":"rs980035744","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588918,"feature_type":"variation","strand":1,"end":140588918,"alleles":["T","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1798898932"},{"end":140588919,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140588919,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798899080"},{"start":140588924,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140588924,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130653322","clinical_significance":[]},{"start":140588927,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140588927,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1681781","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1306699673","feature_type":"variation","strand":1,"end":140588930,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588930},{"end":140588931,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140588931,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs909783718","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588933,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140588933,"seq_region_name":"7","id":"rs1585702108","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588935,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140588935,"id":"rs1798899996","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140588942,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588942,"clinical_significance":[],"seq_region_name":"7","id":"rs1367850758"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1001594848","alleles":["T","C"],"end":140588944,"feature_type":"variation","strand":1,"source":"dbSNP","start":140588944,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140588947,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140588947,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs963403196"},{"alleles":["G","A"],"end":140588948,"strand":1,"feature_type":"variation","start":140588948,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs767642917","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798900912","source":"dbSNP","start":140588950,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140588950,"alleles":["C","G"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588952,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140588952,"clinical_significance":[],"seq_region_name":"7","id":"rs973395100"},{"seq_region_name":"7","id":"rs60901124","clinical_significance":[],"start":140588954,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140588954,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1304149952","clinical_significance":[],"start":140588955,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140588955,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798901483","feature_type":"variation","strand":1,"end":140588956,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588956},{"seq_region_name":"7","id":"rs529082205","clinical_significance":[],"end":140588957,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140588957,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["T","A"],"end":140588959,"strand":1,"feature_type":"variation","start":140588959,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1409712312","clinical_significance":[]},{"id":"rs929384405","seq_region_name":"7","clinical_significance":[],"start":140588962,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140588962,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"alleles":["T","C"],"end":140588970,"feature_type":"variation","strand":1,"source":"dbSNP","start":140588970,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs547556979"},{"start":140588972,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140588972,"alleles":["A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585702219","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588976,"source":"dbSNP","strand":1,"feature_type":"variation","end":140588976,"alleles":["C","T"],"seq_region_name":"7","id":"rs762904015","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798902351","clinical_significance":[],"start":140588977,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","-"],"end":140588977,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140588978,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140588978,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798902451"},{"start":140588981,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140588981,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1433629769","clinical_significance":[]},{"seq_region_name":"7","id":"rs1051827158","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140588987,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140588987},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140588989,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588989,"clinical_significance":[],"seq_region_name":"7","id":"rs2130653500"},{"clinical_significance":[],"id":"rs912064469","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588990,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140588990},{"source":"dbSNP","start":140588991,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140588991,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1014954033"},{"clinical_significance":[],"id":"rs1349346200","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140588992,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140588992},{"alleles":["C","T"],"end":140588997,"strand":1,"feature_type":"variation","start":140588997,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs766109416","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","C"],"end":140589012,"feature_type":"variation","strand":1,"source":"dbSNP","start":140589012,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1317112476"},{"seq_region_name":"7","id":"rs1468222533","clinical_significance":[],"end":140589018,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140589018,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1248680342","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140589019,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589019,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589021,"source":"dbSNP","strand":1,"feature_type":"variation","end":140589021,"alleles":["G","C"],"id":"rs2130653542","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140589022,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140589022,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs566059324"},{"start":140589023,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140589023,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs539895941","clinical_significance":[]},{"source":"dbSNP","start":140589025,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140589025,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1798904423","seq_region_name":"7"},{"start":140589027,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140589027,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs976322039","clinical_significance":[]},{"id":"rs1798904886","seq_region_name":"7","clinical_significance":[],"alleles":["C","A"],"end":140589037,"strand":1,"feature_type":"variation","start":140589037,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["C","T"],"end":140589038,"feature_type":"variation","strand":1,"source":"dbSNP","start":140589038,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs551490483","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140589039,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589039,"source":"dbSNP","seq_region_name":"7","id":"rs1798905240","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798905350","clinical_significance":[],"alleles":["G","A"],"end":140589040,"strand":1,"feature_type":"variation","start":140589040,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1463866719","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589042,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140589042},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798905602","feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140589043,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589043},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589044,"feature_type":"variation","strand":1,"end":140589044,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs932156942"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130653631","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140589045,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589045},{"source":"dbSNP","start":140589046,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140589046,"alleles":["T","A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1231557695","seq_region_name":"7"},{"end":140589047,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140589047,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130653654","clinical_significance":[]},{"seq_region_name":"7","id":"rs1188419520","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589050,"source":"dbSNP","strand":1,"feature_type":"variation","end":140589050,"alleles":["C","T"]},{"id":"rs2130653679","seq_region_name":"7","clinical_significance":[],"alleles":["A","C"],"end":140589051,"strand":1,"feature_type":"variation","start":140589051,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585702410","end":140589052,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140589052,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589053,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140589053,"seq_region_name":"7","id":"rs1369825250","clinical_significance":[]},{"alleles":["T","C"],"end":140589059,"strand":1,"feature_type":"variation","start":140589059,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs985185719","clinical_significance":[]},{"source":"dbSNP","start":140589064,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140589064,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs2130653715","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589065,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140589065,"clinical_significance":[],"seq_region_name":"7","id":"rs2130653718"},{"start":140589068,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140589068,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130653728","clinical_significance":[]},{"start":140589074,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140589074,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1254180908","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130653752","clinical_significance":[],"end":140589079,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140589079,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs2130653757","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589080,"feature_type":"variation","strand":1,"end":140589080,"alleles":["A","T"]},{"id":"rs1386357758","seq_region_name":"7","clinical_significance":[],"start":140589081,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140589081,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"start":140589083,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140589083,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798907002","clinical_significance":[]},{"id":"rs1798907115","seq_region_name":"7","clinical_significance":[],"start":140589090,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140589090,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1798907228","clinical_significance":[],"start":140589092,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140589092,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130653791","feature_type":"variation","strand":1,"end":140589094,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589094},{"feature_type":"variation","strand":1,"end":140589096,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589096,"clinical_significance":[],"seq_region_name":"7","id":"rs2130653794"},{"strand":1,"feature_type":"variation","alleles":["G","C","T"],"end":140589098,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589098,"source":"dbSNP","seq_region_name":"7","id":"rs1455612199","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1039288859","source":"dbSNP","start":140589099,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140589099,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1424610193","feature_type":"variation","strand":1,"end":140589104,"alleles":["G","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589104},{"end":140589105,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140589105,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1466504681"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589107,"feature_type":"variation","strand":1,"end":140589107,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1360637335"},{"id":"rs1798908039","seq_region_name":"7","clinical_significance":[],"start":140589108,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140589108,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs904774371","end":140589110,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140589110,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1453968984","clinical_significance":[],"alleles":["A","G"],"end":140589118,"strand":1,"feature_type":"variation","start":140589118,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130653857","alleles":["G","T"],"end":140589119,"feature_type":"variation","strand":1,"source":"dbSNP","start":140589119,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140589120,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140589120,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1053182059","clinical_significance":[]},{"seq_region_name":"7","id":"rs756605984","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["GTG","G"],"end":140589122,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589120,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798908676","feature_type":"variation","strand":1,"end":140589122,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589122},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589125,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140589125,"seq_region_name":"7","id":"rs1447803477","clinical_significance":[]},{"id":"rs2130653888","seq_region_name":"7","clinical_significance":[],"alleles":["T","A"],"end":140589129,"strand":1,"feature_type":"variation","start":140589129,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140589131,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G","T"],"end":140589131,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs935706618"},{"end":140589134,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140589134,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130653908","clinical_significance":[]},{"seq_region_name":"7","id":"rs1484538461","clinical_significance":[],"alleles":["C","G"],"end":140589136,"strand":1,"feature_type":"variation","start":140589136,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["G","A"],"end":140589138,"feature_type":"variation","strand":1,"source":"dbSNP","start":140589138,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1326422997","seq_region_name":"7"},{"end":140589140,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140589140,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1798909336","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs767121854","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589141,"feature_type":"variation","strand":1,"end":140589141,"alleles":["C","G","T"]},{"id":"rs77989493","seq_region_name":"7","clinical_significance":[],"start":140589142,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C"],"end":140589142,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140589146,"alleles":["GG","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589145,"source":"dbSNP","id":"rs905655337","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589146,"feature_type":"variation","strand":1,"end":140589146,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130653967"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589157,"source":"dbSNP","strand":1,"feature_type":"variation","end":140589157,"alleles":["G","A"],"seq_region_name":"7","id":"rs1324116726","clinical_significance":[]},{"start":140589164,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140589164,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1373510344","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140589168,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589168,"clinical_significance":[],"id":"rs150979578","seq_region_name":"7"},{"source":"dbSNP","start":140589169,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140589169,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1798910279","seq_region_name":"7"},{"source":"dbSNP","start":140589171,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140589171,"alleles":["T","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798910393"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130654005","feature_type":"variation","strand":1,"end":140589181,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589181},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589182,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140589182,"clinical_significance":[],"id":"rs75075230","seq_region_name":"7"},{"source":"dbSNP","start":140589182,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140589184,"alleles":["GGG","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798910685"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130654025","source":"dbSNP","start":140589183,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140589183,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs2130654038","seq_region_name":"7","source":"dbSNP","start":140589190,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140589190,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140589196,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589196,"clinical_significance":[],"id":"rs905720573","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589197,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140589197,"seq_region_name":"7","id":"rs887846703","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589199,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140589199,"seq_region_name":"7","id":"rs1327433909","clinical_significance":[]},{"alleles":["G","A"],"end":140589212,"strand":1,"feature_type":"variation","start":140589212,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1004990749","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798911248","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140589213,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589213},{"clinical_significance":[],"id":"rs1371393699","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589215,"feature_type":"variation","strand":1,"alleles":["-","CTGAGA"],"end":140589214},{"clinical_significance":[],"id":"rs1170644296","seq_region_name":"7","source":"dbSNP","start":140589215,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140589215,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140589217,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140589217,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1428078675"},{"seq_region_name":"7","id":"rs1208529925","clinical_significance":[],"strand":1,"feature_type":"variation","end":140589218,"alleles":["T","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589218,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589231,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140589231,"id":"rs1798911844","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1563162196","clinical_significance":[],"alleles":["C","A"],"end":140589233,"strand":1,"feature_type":"variation","start":140589233,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs73736632","seq_region_name":"7","clinical_significance":[],"end":140589234,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140589234,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589235,"feature_type":"variation","strand":1,"end":140589235,"alleles":["T","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1798912102"},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140589237,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589237,"source":"dbSNP","seq_region_name":"7","id":"rs1798912217","clinical_significance":[]},{"start":140589238,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140589238,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1426037630","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589245,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140589245,"seq_region_name":"7","id":"rs966030190","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589248,"feature_type":"variation","strand":1,"end":140589248,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1470202990"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798912751","source":"dbSNP","start":140589256,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140589256,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs976271085","end":140589257,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140589257,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140589260,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589260,"clinical_significance":[],"seq_region_name":"7","id":"rs1483549830"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589267,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140589267,"clinical_significance":[],"id":"rs1798913184","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1798913307","clinical_significance":[],"alleles":["A","G"],"end":140589269,"strand":1,"feature_type":"variation","start":140589269,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140589270,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140589270,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1016896301"},{"start":140589280,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C","T"],"end":140589280,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs962618377","clinical_significance":[]},{"end":140589283,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140589283,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798913732"},{"clinical_significance":[],"seq_region_name":"7","id":"rs534921028","end":140589287,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140589287,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589288,"feature_type":"variation","strand":1,"end":140589288,"alleles":["C","A"],"clinical_significance":[],"id":"rs953691823","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140589289,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589289,"source":"dbSNP","id":"rs2130654212","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1337080534","clinical_significance":[],"alleles":["C","G"],"end":140589294,"strand":1,"feature_type":"variation","start":140589294,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1798914231","seq_region_name":"7","feature_type":"variation","strand":1,"end":140589296,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589296},{"clinical_significance":[],"seq_region_name":"7","id":"rs1026741825","feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140589301,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589301},{"feature_type":"variation","strand":1,"end":140589302,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589302,"clinical_significance":[],"seq_region_name":"7","id":"rs1244946068"},{"strand":1,"feature_type":"variation","end":140589308,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589308,"source":"dbSNP","seq_region_name":"7","id":"rs980000245","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589315,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140589315,"seq_region_name":"7","id":"rs1798914783","clinical_significance":[]},{"seq_region_name":"7","id":"rs950723330","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589316,"source":"dbSNP","strand":1,"feature_type":"variation","end":140589316,"alleles":["A","C","G"]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140589318,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589318,"source":"dbSNP","id":"rs1798915074","seq_region_name":"7","clinical_significance":[]},{"id":"rs1798915184","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589321,"source":"dbSNP","strand":1,"feature_type":"variation","end":140589321,"alleles":["A","C"]},{"seq_region_name":"7","id":"rs754338624","clinical_significance":[],"end":140589322,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140589322,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140589323,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140589323,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130654279","clinical_significance":[]},{"id":"rs757844056","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140589325,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589325,"source":"dbSNP"},{"alleles":["T","G"],"end":140589332,"feature_type":"variation","strand":1,"source":"dbSNP","start":140589332,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1309645562"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140589337,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589337,"clinical_significance":[],"seq_region_name":"7","id":"rs1798915669"},{"seq_region_name":"7","id":"rs1798915784","clinical_significance":[],"start":140589339,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140589339,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"start":140589341,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140589341,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs73736633","clinical_significance":[]},{"seq_region_name":"7","id":"rs1396457308","clinical_significance":[],"start":140589342,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140589342,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1163885370","feature_type":"variation","strand":1,"end":140589346,"alleles":["A","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589346},{"end":140589347,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140589347,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1459560397","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589352,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140589352,"clinical_significance":[],"seq_region_name":"7","id":"rs1416324092"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1164767135","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140589354,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589354},{"seq_region_name":"7","id":"rs974878047","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589359,"source":"dbSNP","strand":1,"feature_type":"variation","end":140589359,"alleles":["C","T"]},{"clinical_significance":[],"id":"rs926082459","seq_region_name":"7","end":140589360,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140589360,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1798916849","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589362,"source":"dbSNP","strand":1,"feature_type":"variation","end":140589362,"alleles":["T","A"]},{"end":140589364,"alleles":["C","A","G"],"strand":1,"feature_type":"variation","start":140589364,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs936262446","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798917077","end":140589365,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140589365,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1249457997","alleles":["G","C"],"end":140589368,"feature_type":"variation","strand":1,"source":"dbSNP","start":140589368,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140589370,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140589370,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798917315","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589371,"source":"dbSNP","strand":1,"feature_type":"variation","end":140589371,"alleles":["A","T"],"seq_region_name":"7","id":"rs1798917457","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798917583","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589374,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140589374},{"clinical_significance":[],"id":"rs2130654415","seq_region_name":"7","end":140589380,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140589380,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589389,"feature_type":"variation","strand":1,"end":140589389,"alleles":["A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1053343795"},{"seq_region_name":"7","id":"rs891475836","clinical_significance":[],"strand":1,"feature_type":"variation","end":140589390,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589390,"source":"dbSNP"},{"id":"rs1209910361","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140589391,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589391,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589401,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140589401,"seq_region_name":"7","id":"rs1354555040","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589407,"feature_type":"variation","strand":1,"end":140589407,"alleles":["G","A"],"clinical_significance":[],"id":"rs572048613","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140589408,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589408,"clinical_significance":[],"seq_region_name":"7","id":"rs1798918294"},{"seq_region_name":"7","id":"rs1798918419","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589415,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140589415},{"clinical_significance":[],"seq_region_name":"7","id":"rs1270738421","alleles":["T","C"],"end":140589419,"feature_type":"variation","strand":1,"source":"dbSNP","start":140589419,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589420,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140589420,"clinical_significance":[],"seq_region_name":"7","id":"rs949705311"},{"seq_region_name":"7","id":"rs545842793","clinical_significance":[],"start":140589421,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140589421,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"id":"rs1798918749","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140589423,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589423,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140589424,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589424,"source":"dbSNP","seq_region_name":"7","id":"rs76992035","clinical_significance":[]},{"end":140589426,"alleles":["A","C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140589426,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs746291132"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130654504","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589437,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140589437},{"clinical_significance":[],"id":"rs1335383702","seq_region_name":"7","source":"dbSNP","start":140589443,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140589443,"alleles":["G","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1798919313","clinical_significance":[],"start":140589443,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["GGGGG","GGGG"],"end":140589447,"strand":1,"feature_type":"variation"},{"alleles":["G","A"],"end":140589444,"feature_type":"variation","strand":1,"source":"dbSNP","start":140589444,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1294258457"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589455,"feature_type":"variation","strand":1,"end":140589455,"alleles":["G","C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1001409845"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589456,"feature_type":"variation","strand":1,"end":140589456,"alleles":["G","C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs372750841"},{"feature_type":"variation","strand":1,"end":140589457,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589457,"clinical_significance":[],"seq_region_name":"7","id":"rs1016780564"},{"clinical_significance":[],"id":"rs1798919941","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140589458,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589458},{"source":"dbSNP","start":140589459,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140589459,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798920050"},{"source":"dbSNP","start":140589462,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140589462,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798920167"},{"strand":1,"feature_type":"variation","alleles":["TC","-"],"end":140589465,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589464,"source":"dbSNP","seq_region_name":"7","id":"rs1735947631","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798920282","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589467,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140589467},{"clinical_significance":[],"id":"rs1798920407","seq_region_name":"7","end":140589469,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140589469,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1798920526","clinical_significance":[],"start":140589474,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140589474,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1798920636","clinical_significance":[],"end":140589478,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140589478,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140589479,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589479,"source":"dbSNP","seq_region_name":"7","id":"rs898298558","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1005346755","feature_type":"variation","strand":1,"end":140589481,"alleles":["G","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589481},{"strand":1,"feature_type":"variation","end":140589485,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589485,"source":"dbSNP","seq_region_name":"7","id":"rs1798921032","clinical_significance":[]},{"clinical_significance":[],"id":"rs1458201293","seq_region_name":"7","end":140589491,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140589491,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["T","C","G"],"end":140589494,"strand":1,"feature_type":"variation","start":140589494,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs994509664","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589497,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140589497,"clinical_significance":[],"id":"rs140811231","seq_region_name":"7"},{"id":"rs758673437","seq_region_name":"7","clinical_significance":[],"start":140589498,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140589498,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563162318","source":"dbSNP","start":140589504,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140589504,"feature_type":"variation","strand":1},{"start":140589505,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140589505,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1207425863","clinical_significance":[]},{"start":140589508,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140589508,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1036412705","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130654666","clinical_significance":[],"end":140589517,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140589517,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140589531,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140589531,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs561682085"},{"alleles":["T","G"],"end":140589533,"strand":1,"feature_type":"variation","start":140589533,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs529120145","clinical_significance":[]},{"id":"rs1798922235","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140589534,"strand":1,"feature_type":"variation","start":140589534,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs2130654700","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140589537,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589537,"source":"dbSNP"},{"id":"rs1798922345","seq_region_name":"7","clinical_significance":[],"end":140589538,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140589538,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs2130654714","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589546,"source":"dbSNP","strand":1,"feature_type":"variation","end":140589546,"alleles":["A","G"]},{"source":"dbSNP","start":140589548,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140589548,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs2130654727","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140589550,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589550,"clinical_significance":[],"seq_region_name":"7","id":"rs1798922464"},{"seq_region_name":"7","id":"rs2130654747","clinical_significance":[],"start":140589552,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140589552,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140589553,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589553,"source":"dbSNP","seq_region_name":"7","id":"rs987481139","clinical_significance":[]},{"seq_region_name":"7","id":"rs77840185","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140589555,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589555,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs997467333","source":"dbSNP","start":140589556,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140589556,"feature_type":"variation","strand":1},{"id":"rs1798922955","seq_region_name":"7","clinical_significance":[],"alleles":["A","G"],"end":140589557,"strand":1,"feature_type":"variation","start":140589557,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1798923091","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140589571,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589571,"source":"dbSNP"},{"source":"dbSNP","start":140589572,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140589572,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798923198"},{"strand":1,"feature_type":"variation","end":140589574,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589574,"source":"dbSNP","seq_region_name":"7","id":"rs112266103","clinical_significance":[]},{"seq_region_name":"7","id":"rs974762293","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589575,"source":"dbSNP","strand":1,"feature_type":"variation","end":140589575,"alleles":["C","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589577,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140589577,"clinical_significance":[],"seq_region_name":"7","id":"rs533278021"},{"source":"dbSNP","start":140589582,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140589582,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130654810"},{"feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140589583,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589583,"clinical_significance":[],"seq_region_name":"7","id":"rs1235643058"},{"strand":1,"feature_type":"variation","alleles":["GAGAGAGAGA","GAGAGA","GAGAGAGAGAGA"],"end":140589593,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589584,"source":"dbSNP","seq_region_name":"7","id":"rs1420176075","clinical_significance":[]},{"start":140589585,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140589585,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798923931","clinical_significance":[]},{"start":140589586,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140589586,"alleles":["G","C","T"],"strand":1,"feature_type":"variation","id":"rs1411104990","seq_region_name":"7","clinical_significance":[]},{"id":"rs1798924179","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589589,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140589589},{"seq_region_name":"7","id":"rs1798924315","clinical_significance":[],"start":140589590,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140589590,"strand":1,"feature_type":"variation"},{"end":140589595,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140589595,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798924424"},{"alleles":["G","C"],"end":140589597,"feature_type":"variation","strand":1,"source":"dbSNP","start":140589597,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1302741535","seq_region_name":"7"},{"end":140589602,"alleles":["GGCTG","GGCTGGCTG"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140589598,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1563162371"},{"id":"rs1305617777","seq_region_name":"7","clinical_significance":[],"end":140589599,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140589599,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs936150384","seq_region_name":"7","feature_type":"variation","strand":1,"end":140589600,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589600},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585703425","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589601,"feature_type":"variation","strand":1,"end":140589601,"alleles":["T","C"]},{"id":"rs1798925844","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140589602,"strand":1,"feature_type":"variation","start":140589602,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1391468593","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140589605,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589605},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140589609,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589609,"source":"dbSNP","id":"rs1798926215","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140589611,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589611,"source":"dbSNP","seq_region_name":"7","id":"rs551610986","clinical_significance":[]},{"clinical_significance":[],"id":"rs1400648998","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589612,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140589612},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798926822","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589615,"feature_type":"variation","strand":1,"end":140589615,"alleles":["G","A"]},{"start":140589616,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140589616,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1403293410","clinical_significance":[]},{"alleles":["C","T"],"end":140589621,"feature_type":"variation","strand":1,"source":"dbSNP","start":140589621,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1174706371","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140589627,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589627,"source":"dbSNP","seq_region_name":"7","id":"rs1415014719","clinical_significance":[]},{"seq_region_name":"7","id":"rs768571493","clinical_significance":[],"end":140589628,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140589628,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140589632,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140589632,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs949790238","clinical_significance":[]},{"seq_region_name":"7","id":"rs1314392565","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589636,"source":"dbSNP","strand":1,"feature_type":"variation","end":140589644,"alleles":["TATTTATTT","TATTT"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs74997615","feature_type":"variation","strand":1,"end":140589637,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589637},{"end":140589638,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140589638,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs149724200"},{"id":"rs1798928406","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589641,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140589641},{"id":"rs1798928522","seq_region_name":"7","clinical_significance":[],"end":140589646,"alleles":["TTTTT","TTTTTT"],"strand":1,"feature_type":"variation","start":140589642,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["T","C"],"end":140589643,"feature_type":"variation","strand":1,"source":"dbSNP","start":140589643,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1446290252","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140589649,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589649,"source":"dbSNP","seq_region_name":"7","id":"rs912983748","clinical_significance":[]},{"seq_region_name":"7","id":"rs749160953","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589651,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140589651},{"seq_region_name":"7","id":"rs1798929042","clinical_significance":[],"end":140589652,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140589652,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs937081983","alleles":["G","C"],"end":140589654,"feature_type":"variation","strand":1,"source":"dbSNP","start":140589654,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1279033099","seq_region_name":"7","source":"dbSNP","start":140589655,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140589655,"feature_type":"variation","strand":1},{"start":140589656,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140589656,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1202016866","clinical_significance":[]},{"start":140589659,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140589659,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs549362783","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140589662,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589662,"clinical_significance":[],"id":"rs117836110","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589664,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140589664,"clinical_significance":[],"seq_region_name":"7","id":"rs1798929752"},{"end":140589666,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140589666,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798929882"},{"seq_region_name":"7","id":"rs981090989","clinical_significance":[],"start":140589669,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140589669,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589678,"source":"dbSNP","strand":1,"feature_type":"variation","end":140589678,"alleles":["G","A"],"seq_region_name":"7","id":"rs528039003","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140589680,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589680,"source":"dbSNP","id":"rs1798930262","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1268511421","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589688,"source":"dbSNP","strand":1,"feature_type":"variation","end":140589688,"alleles":["G","A"]},{"id":"rs1367376830","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589688,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GG","G"],"end":140589689},{"end":140589689,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140589689,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798930576"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798930685","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589694,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140589694},{"source":"dbSNP","start":140589695,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140589695,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1430588779"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589701,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140589701,"clinical_significance":[],"id":"rs1341630261","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1336528838","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589702,"feature_type":"variation","strand":1,"end":140589702,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs61369053","clinical_significance":[],"end":140589706,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140589706,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589707,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140589707,"clinical_significance":[],"seq_region_name":"7","id":"rs578154495"},{"start":140589708,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140589708,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798931477","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs770776667","alleles":["C","A","T"],"end":140589711,"feature_type":"variation","strand":1,"source":"dbSNP","start":140589711,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs891041698","end":140589716,"alleles":["A","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140589716,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589717,"source":"dbSNP","strand":1,"feature_type":"variation","end":140589717,"alleles":["T","C","G"],"seq_region_name":"7","id":"rs1798931934","clinical_significance":[]},{"seq_region_name":"7","id":"rs375364053","clinical_significance":[],"strand":1,"feature_type":"variation","end":140589721,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589721,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140589722,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589722,"source":"dbSNP","seq_region_name":"7","id":"rs1798932210","clinical_significance":[]},{"seq_region_name":"7","id":"rs1211791638","clinical_significance":[],"alleles":["G","C"],"end":140589723,"strand":1,"feature_type":"variation","start":140589723,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140589724,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589724,"source":"dbSNP","seq_region_name":"7","id":"rs1165693759","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1475031199","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589725,"feature_type":"variation","strand":1,"end":140589725,"alleles":["C","G"]},{"seq_region_name":"7","id":"rs1238041776","clinical_significance":[],"strand":1,"feature_type":"variation","end":140589727,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589727,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1189798703","clinical_significance":[],"start":140589731,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140589731,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1798932934","clinical_significance":[],"start":140589734,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140589734,"strand":1,"feature_type":"variation"},{"id":"rs1008520947","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140589735,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589735,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1798933169","seq_region_name":"7","source":"dbSNP","start":140589736,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140589736,"alleles":["C","A"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140589738,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140589738,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1798933311","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1018908136","seq_region_name":"7","feature_type":"variation","strand":1,"end":140589742,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589742},{"feature_type":"variation","strand":1,"end":140589743,"alleles":["T","C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589743,"clinical_significance":[],"seq_region_name":"7","id":"rs1798933557"},{"clinical_significance":[],"seq_region_name":"7","id":"rs538855270","end":140589752,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140589752,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140589753,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589753,"source":"dbSNP","seq_region_name":"7","id":"rs1440439547","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs996233210","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140589754,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589754},{"clinical_significance":[],"seq_region_name":"7","id":"rs1206074925","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589759,"feature_type":"variation","strand":1,"end":140589759,"alleles":["G","A"]},{"alleles":["G","C"],"end":140589764,"feature_type":"variation","strand":1,"source":"dbSNP","start":140589764,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs940538055"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1033040895","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589766,"feature_type":"variation","strand":1,"end":140589766,"alleles":["C","A"]},{"seq_region_name":"7","id":"rs1585703859","clinical_significance":[],"start":140589769,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140589769,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140589772,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140589772,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1214107103","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1585703876","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589775,"feature_type":"variation","strand":1,"end":140589775,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1585703892","clinical_significance":[],"strand":1,"feature_type":"variation","end":140589777,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589777,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1798934959","clinical_significance":[],"start":140589785,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140589785,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1357654721","source":"dbSNP","start":140589786,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140589786,"alleles":["G","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1286532935","clinical_significance":[],"strand":1,"feature_type":"variation","end":140589788,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589788,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140589790,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589790,"source":"dbSNP","seq_region_name":"7","id":"rs1798935323","clinical_significance":[]},{"source":"dbSNP","start":140589792,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140589792,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1798935455","seq_region_name":"7"},{"id":"rs2130655349","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140589796,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589796,"source":"dbSNP"},{"start":140589800,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140589800,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798935591","clinical_significance":[]},{"source":"dbSNP","start":140589810,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140589810,"alleles":["T","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798935699"},{"clinical_significance":[],"id":"rs1413476650","seq_region_name":"7","end":140589811,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140589811,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140589812,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140589812,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs957803284","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1355155001","end":140589815,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140589815,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589816,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140589816,"clinical_significance":[],"seq_region_name":"7","id":"rs1798936168"},{"id":"rs1798936283","seq_region_name":"7","clinical_significance":[],"start":140589820,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140589820,"strand":1,"feature_type":"variation"},{"id":"rs988987597","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140589822,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589822,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["T","-"],"end":140589822,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589822,"source":"dbSNP","id":"rs1476333914","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1309053215","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589826,"source":"dbSNP","strand":1,"feature_type":"variation","end":140589826,"alleles":["G","A","T"]},{"start":140589829,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140589829,"strand":1,"feature_type":"variation","id":"rs1798937075","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs759362140","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589832,"feature_type":"variation","strand":1,"end":140589832,"alleles":["C","T"]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140589835,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589835,"clinical_significance":[],"seq_region_name":"7","id":"rs1389000567"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589839,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140589839,"seq_region_name":"7","id":"rs2130655427","clinical_significance":[]},{"source":"dbSNP","start":140589843,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140589843,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1036189858","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140589844,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589844,"clinical_significance":[],"seq_region_name":"7","id":"rs1798937824"},{"alleles":["C","G"],"end":140589846,"feature_type":"variation","strand":1,"source":"dbSNP","start":140589846,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798937956"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589853,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140589853,"seq_region_name":"7","id":"rs1326264340","clinical_significance":[]},{"id":"rs901925348","seq_region_name":"7","clinical_significance":[],"end":140589856,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140589856,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1798938353","clinical_significance":[],"alleles":["G","C"],"end":140589857,"strand":1,"feature_type":"variation","start":140589857,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798938475","source":"dbSNP","start":140589861,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140589861,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1413897838","feature_type":"variation","strand":1,"alleles":["C","A","G","T"],"end":140589866,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589866},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798938764","end":140589867,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140589867,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140589871,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589871,"source":"dbSNP","seq_region_name":"7","id":"rs997583464","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1434816372","source":"dbSNP","start":140589873,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140589873,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589880,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140589880,"clinical_significance":[],"id":"rs1798939186","seq_region_name":"7"},{"seq_region_name":"7","id":"rs913515869","clinical_significance":[],"strand":1,"feature_type":"variation","end":140589882,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589882,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798939394","alleles":["C","T"],"end":140589884,"feature_type":"variation","strand":1,"source":"dbSNP","start":140589884,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140589895,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140589895,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798939491","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589896,"source":"dbSNP","strand":1,"feature_type":"variation","end":140589896,"alleles":["T","C"],"seq_region_name":"7","id":"rs971676806","clinical_significance":[]},{"clinical_significance":[],"id":"rs2130655536","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589901,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140589901},{"alleles":["T","C"],"end":140589907,"feature_type":"variation","strand":1,"source":"dbSNP","start":140589907,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1474199602","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589908,"source":"dbSNP","strand":1,"feature_type":"variation","end":140589908,"alleles":["T","A"],"seq_region_name":"7","id":"rs1798939819","clinical_significance":[]},{"alleles":["TTTTT","TTTT","TTTTTT"],"end":140589916,"feature_type":"variation","strand":1,"source":"dbSNP","start":140589912,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1416843784"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1175059133","end":140589915,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140589915,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["T","C"],"end":140589918,"strand":1,"feature_type":"variation","start":140589918,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1481726120","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1231447492","end":140589923,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140589923,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1203908579","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589924,"feature_type":"variation","strand":1,"end":140589924,"alleles":["A","T"]},{"seq_region_name":"7","id":"rs1798940600","clinical_significance":[],"end":140589927,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140589927,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589929,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140589929,"seq_region_name":"7","id":"rs192118563","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140589931,"alleles":["C","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589931,"source":"dbSNP","seq_region_name":"7","id":"rs1452183268","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs184669224","feature_type":"variation","strand":1,"end":140589933,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589933},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798941052","alleles":["A","G"],"end":140589942,"feature_type":"variation","strand":1,"source":"dbSNP","start":140589942,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1231942580","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589950,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140589950},{"seq_region_name":"7","id":"rs1798941280","clinical_significance":[],"end":140589951,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140589951,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1798941407","clinical_significance":[],"alleles":["A","C"],"end":140589952,"strand":1,"feature_type":"variation","start":140589952,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798941507","alleles":["G","C"],"end":140589953,"feature_type":"variation","strand":1,"source":"dbSNP","start":140589953,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140589955,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140589955,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs889138039","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798941741","end":140589956,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140589956,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589957,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AAATTTCGAAAT","AAAT"],"end":140589968,"seq_region_name":"7","id":"rs1798941838","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140589958,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589958,"clinical_significance":[],"seq_region_name":"7","id":"rs2130655654"},{"source":"dbSNP","start":140589959,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140589959,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs76598568","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589962,"source":"dbSNP","strand":1,"feature_type":"variation","end":140589962,"alleles":["T","C"],"seq_region_name":"7","id":"rs1798942070","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589963,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140589963,"id":"rs561323093","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140589964,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589964,"source":"dbSNP","seq_region_name":"7","id":"rs57561934","clinical_significance":[]},{"alleles":["T","C","G"],"end":140589968,"feature_type":"variation","strand":1,"source":"dbSNP","start":140589968,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1441046047"},{"end":140589969,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140589969,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798942660"},{"alleles":["A","T"],"end":140589970,"feature_type":"variation","strand":1,"source":"dbSNP","start":140589970,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs559381978"},{"id":"rs775795623","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140589972,"alleles":["A","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589972,"source":"dbSNP"},{"id":"rs1798943025","seq_region_name":"7","clinical_significance":[],"start":140589975,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140589975,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140589979,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589979,"clinical_significance":[],"id":"rs763443898","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140589981,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589981,"clinical_significance":[],"id":"rs1798943237","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140589990,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589990,"source":"dbSNP","id":"rs2130655741","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs929838494","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589992,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140589992},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589993,"feature_type":"variation","strand":1,"end":140589993,"alleles":["C","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1364461127"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589994,"feature_type":"variation","strand":1,"end":140589994,"alleles":["T","C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs145591684"},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140589996,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140589996,"clinical_significance":[],"seq_region_name":"7","id":"rs775435435"},{"id":"rs1798943963","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140589997,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140589997},{"seq_region_name":"7","id":"rs890917137","clinical_significance":[],"start":140589999,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140589999,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"alleles":["T","C"],"end":140590002,"feature_type":"variation","strand":1,"source":"dbSNP","start":140590002,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1459779271"},{"clinical_significance":[],"seq_region_name":"7","id":"rs753463423","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590006,"feature_type":"variation","strand":1,"end":140590006,"alleles":["A","T"]},{"id":"rs1798944439","seq_region_name":"7","clinical_significance":[],"start":140590007,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140590007,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798944540","end":140590015,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140590015,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590018,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","G"],"end":140590018,"seq_region_name":"7","id":"rs1393701942","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140590021,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590021,"clinical_significance":[],"seq_region_name":"7","id":"rs2130655832"},{"end":140590022,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140590022,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs2130655838","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs140413334","end":140590026,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140590026,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1420722750","seq_region_name":"7","clinical_significance":[],"alleles":["AACAACA","AACA"],"end":140590034,"strand":1,"feature_type":"variation","start":140590028,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1798944904","clinical_significance":[],"strand":1,"feature_type":"variation","end":140590029,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590029,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590032,"feature_type":"variation","strand":1,"end":140590032,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs563785361"},{"alleles":["G","A"],"end":140590035,"strand":1,"feature_type":"variation","start":140590035,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs2130655882","seq_region_name":"7","clinical_significance":[]},{"start":140590038,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140590038,"strand":1,"feature_type":"variation","id":"rs1039570987","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140590040,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590040,"source":"dbSNP","seq_region_name":"7","id":"rs1405527246","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590042,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140590042,"clinical_significance":[],"seq_region_name":"7","id":"rs1798945418"},{"seq_region_name":"7","id":"rs1798945524","clinical_significance":[],"end":140590043,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140590043,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1343109489","clinical_significance":[],"start":140590045,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140590045,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"id":"rs1200134355","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590046,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140590046},{"seq_region_name":"7","id":"rs1798945841","clinical_significance":[],"end":140590047,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140590047,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs981208489","end":140590048,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140590048,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1478491620","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140590056,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590056,"source":"dbSNP"},{"start":140590057,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C","T"],"end":140590057,"strand":1,"feature_type":"variation","id":"rs900536193","seq_region_name":"7","clinical_significance":[]},{"end":140590068,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140590068,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs73500409"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590070,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140590070,"clinical_significance":[],"seq_region_name":"7","id":"rs1466134464"},{"source":"dbSNP","start":140590073,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140590073,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs958406044"},{"seq_region_name":"7","id":"rs1269397667","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140590074,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590074,"source":"dbSNP"},{"source":"dbSNP","start":140590075,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140590075,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1247348615"},{"source":"dbSNP","start":140590077,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140590077,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs866419133","seq_region_name":"7"},{"end":140590079,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140590079,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130656020","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590080,"source":"dbSNP","strand":1,"feature_type":"variation","end":140590080,"alleles":["C","T"],"seq_region_name":"7","id":"rs1454304256","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590082,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140590082,"seq_region_name":"7","id":"rs1222813869","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140590083,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590083,"clinical_significance":[],"seq_region_name":"7","id":"rs1371327325"},{"seq_region_name":"7","id":"rs1200405713","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140590085,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590085,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs549401939","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590086,"feature_type":"variation","strand":1,"end":140590086,"alleles":["T","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs957475753","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140590096,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590096},{"seq_region_name":"7","id":"rs1438148727","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590097,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140590097},{"seq_region_name":"7","id":"rs1798948943","clinical_significance":[],"end":140590099,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140590099,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140590101,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140590101,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1798949055","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","C"],"end":140590104,"strand":1,"feature_type":"variation","start":140590104,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1798949166","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs115782786","source":"dbSNP","start":140590105,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140590105,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs528465532","seq_region_name":"7","feature_type":"variation","strand":1,"end":140590107,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590107},{"alleles":["G","A"],"end":140590108,"feature_type":"variation","strand":1,"source":"dbSNP","start":140590108,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798949873"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590109,"feature_type":"variation","strand":1,"end":140590109,"alleles":["G","C"],"clinical_significance":[],"id":"rs750785967","seq_region_name":"7"},{"end":140590110,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140590110,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1798950099","seq_region_name":"7"},{"end":140590111,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140590111,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs547317486","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1158840559","seq_region_name":"7","source":"dbSNP","start":140590112,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140590112,"alleles":["G","A","T"],"feature_type":"variation","strand":1},{"end":140590115,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140590115,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798950518","clinical_significance":[]},{"seq_region_name":"7","id":"rs758652222","clinical_significance":[],"start":140590116,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140590116,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs780490868","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590117,"feature_type":"variation","strand":1,"end":140590117,"alleles":["C","A","T"]},{"id":"rs189380978","seq_region_name":"7","clinical_significance":[],"start":140590118,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C"],"end":140590118,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1798951127","clinical_significance":[],"alleles":["G","A"],"end":140590119,"strand":1,"feature_type":"variation","start":140590119,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590121,"source":"dbSNP","strand":1,"feature_type":"variation","end":140590121,"alleles":["G","A"],"seq_region_name":"7","id":"rs1319081599","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590123,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140590123,"clinical_significance":[],"id":"rs958392307","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798951510","source":"dbSNP","start":140590127,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A","C"],"end":140590127,"feature_type":"variation","strand":1},{"id":"rs1248741754","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140590131,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590131,"source":"dbSNP"},{"end":140590137,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140590137,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1798951941","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1036139646","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140590138,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590138},{"source":"dbSNP","start":140590139,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140590139,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs923129898"},{"id":"rs1442345241","seq_region_name":"7","clinical_significance":[],"alleles":["A","G"],"end":140590140,"strand":1,"feature_type":"variation","start":140590140,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140590144,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140590144,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798952796","clinical_significance":[]},{"seq_region_name":"7","id":"rs933379781","clinical_significance":[],"strand":1,"feature_type":"variation","end":140590145,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590145,"source":"dbSNP"},{"end":140590147,"alleles":["TTT","TT"],"strand":1,"feature_type":"variation","start":140590145,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798953058","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798953171","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590146,"source":"dbSNP","strand":1,"feature_type":"variation","end":140590146,"alleles":["T","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1211320459","feature_type":"variation","strand":1,"end":140590146,"alleles":["-","GTAA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590147},{"seq_region_name":"7","id":"rs1050481178","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590148,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GGG","GG"],"end":140590150},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798953508","feature_type":"variation","strand":1,"alleles":["-","TAAT"],"end":140590148,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590149},{"clinical_significance":[],"seq_region_name":"7","id":"rs889078122","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140590150,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590150},{"alleles":["A","G"],"end":140590151,"strand":1,"feature_type":"variation","start":140590151,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1303458948","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140590153,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590153,"source":"dbSNP","seq_region_name":"7","id":"rs1798953733","clinical_significance":[]},{"source":"dbSNP","start":140590154,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140590154,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1329486166"},{"id":"rs1798954010","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140590155,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590155,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1232801329","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590156,"source":"dbSNP","strand":1,"feature_type":"variation","end":140590156,"alleles":["G","A","T"]},{"alleles":["A","G"],"end":140590157,"strand":1,"feature_type":"variation","start":140590157,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798954282","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs973731610","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590160,"feature_type":"variation","strand":1,"end":140590160,"alleles":["C","A","G","T"]},{"strand":1,"feature_type":"variation","end":140590161,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590161,"source":"dbSNP","seq_region_name":"7","id":"rs1798954600","clinical_significance":[]},{"clinical_significance":[],"id":"rs919545791","seq_region_name":"7","alleles":["G","A"],"end":140590163,"feature_type":"variation","strand":1,"source":"dbSNP","start":140590163,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs929747214","end":140590164,"alleles":["C","A","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140590164,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs539256560","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590165,"feature_type":"variation","strand":1,"end":140590165,"alleles":["G","A"]},{"start":140590167,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140590167,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585704855","clinical_significance":[]},{"start":140590168,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140590168,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585704863","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798955368","feature_type":"variation","strand":1,"end":140590169,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590169},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585704867","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590170,"feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140590170},{"seq_region_name":"7","id":"rs1390824589","clinical_significance":[],"end":140590176,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140590176,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs959769489","source":"dbSNP","start":140590178,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140590178,"alleles":["T","C","G"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140590180,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140590180,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs557099304"},{"clinical_significance":[],"seq_region_name":"7","id":"rs112306866","source":"dbSNP","start":140590183,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140590183,"alleles":["G","A","T"],"feature_type":"variation","strand":1},{"id":"rs1585704919","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590185,"source":"dbSNP","strand":1,"feature_type":"variation","end":140590185,"alleles":["T","G"]},{"id":"rs1798956321","seq_region_name":"7","clinical_significance":[],"start":140590187,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140590187,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140590189,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590189,"source":"dbSNP","seq_region_name":"7","id":"rs536704323","clinical_significance":[]},{"end":140590193,"alleles":["CC","C"],"strand":1,"feature_type":"variation","start":140590192,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1468831727","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798956723","source":"dbSNP","start":140590196,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140590196,"alleles":["C","T"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590197,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140590197,"clinical_significance":[],"seq_region_name":"7","id":"rs1798956853"},{"seq_region_name":"7","id":"rs560365091","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590201,"source":"dbSNP","strand":1,"feature_type":"variation","end":140590201,"alleles":["C","T"]},{"source":"dbSNP","start":140590202,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140590202,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1798957117","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590206,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140590206,"seq_region_name":"7","id":"rs899753206","clinical_significance":[]},{"end":140590207,"alleles":["T","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140590207,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs932026249"},{"source":"dbSNP","start":140590208,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140590208,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1798957436","seq_region_name":"7"},{"seq_region_name":"7","id":"rs906711409","clinical_significance":[],"alleles":["T","C"],"end":140590210,"strand":1,"feature_type":"variation","start":140590210,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs554954503","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140590215,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590215},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590216,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140590216,"clinical_significance":[],"seq_region_name":"7","id":"rs1002589199"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130656532","alleles":["T","C"],"end":140590217,"feature_type":"variation","strand":1,"source":"dbSNP","start":140590217,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1251350946","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590222,"source":"dbSNP","strand":1,"feature_type":"variation","end":140590222,"alleles":["T","C"]},{"id":"rs1229053412","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140590223,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590223,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140590224,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590224,"clinical_significance":[],"seq_region_name":"7","id":"rs1798958146"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1182014939","feature_type":"variation","strand":1,"end":140590227,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590227},{"clinical_significance":[],"seq_region_name":"7","id":"rs112264339","end":140590228,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140590228,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1294686186","clinical_significance":[],"end":140590231,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140590231,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798958640","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590233,"feature_type":"variation","strand":1,"end":140590233,"alleles":["T","A","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798958797","feature_type":"variation","strand":1,"alleles":["T","A"],"end":140590241,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590241},{"id":"rs1798958921","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590244,"source":"dbSNP","strand":1,"feature_type":"variation","end":140590244,"alleles":["G","C"]},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140590246,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590246,"source":"dbSNP","seq_region_name":"7","id":"rs2130656613","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140590248,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590248,"clinical_significance":[],"seq_region_name":"7","id":"rs1798959048"},{"source":"dbSNP","start":140590252,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140590252,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798959171"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798959335","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590254,"feature_type":"variation","strand":1,"end":140590254,"alleles":["G","C"]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140590256,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590256,"source":"dbSNP","seq_region_name":"7","id":"rs958739427","clinical_significance":[]},{"end":140590259,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140590259,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798959710"},{"seq_region_name":"7","id":"rs1798959851","clinical_significance":[],"strand":1,"feature_type":"variation","end":140590261,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590261,"source":"dbSNP"},{"end":140590262,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140590262,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1010333711"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798960129","end":140590263,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140590263,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140590267,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140590267,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs540644734","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798960352","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590270,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140590270},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798960458","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140590273,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590273},{"end":140590277,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140590277,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1310882363"},{"seq_region_name":"7","id":"rs1414369106","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590279,"source":"dbSNP","strand":1,"feature_type":"variation","end":140590279,"alleles":["A","G"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590282,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140590282,"seq_region_name":"7","id":"rs193227028","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590283,"feature_type":"variation","strand":1,"end":140590283,"alleles":["G","A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs185618576"},{"start":140590289,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140590289,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs1585705142","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs866765388","source":"dbSNP","start":140590293,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140590293,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140590297,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590297,"source":"dbSNP","seq_region_name":"7","id":"rs1295870526","clinical_significance":[]},{"alleles":["G","C"],"end":140590298,"strand":1,"feature_type":"variation","start":140590298,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130656750","clinical_significance":[]},{"end":140590304,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140590304,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs189304119","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs958946682","feature_type":"variation","strand":1,"end":140590305,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590305},{"start":140590307,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C","G"],"end":140590307,"strand":1,"feature_type":"variation","id":"rs1798961778","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798961933","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140590308,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590308},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590312,"source":"dbSNP","strand":1,"feature_type":"variation","end":140590312,"alleles":["C","G"],"id":"rs1798962052","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs974285588","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140590313,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590313},{"end":140590314,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140590314,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs766897951","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798962431","source":"dbSNP","start":140590314,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140590317,"alleles":["GGGG","GGG"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs933159030","clinical_significance":[],"strand":1,"feature_type":"variation","end":140590316,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590316,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1798962656","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140590320,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590320,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1585705226","clinical_significance":[],"strand":1,"feature_type":"variation","end":140590321,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590321,"source":"dbSNP"},{"seq_region_name":"7","id":"rs986410079","clinical_significance":[],"start":140590322,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140590322,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140590323,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590323,"source":"dbSNP","id":"rs563426328","seq_region_name":"7","clinical_significance":[]},{"id":"rs2130656856","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140590325,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590325,"source":"dbSNP"},{"end":140590328,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140590328,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1250881639","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs910630004","source":"dbSNP","start":140590334,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140590334,"feature_type":"variation","strand":1},{"end":140590345,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140590345,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs936782268","seq_region_name":"7","clinical_significance":[]},{"start":140590346,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140590346,"strand":1,"feature_type":"variation","id":"rs1026662675","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590347,"source":"dbSNP","strand":1,"feature_type":"variation","end":140590347,"alleles":["G","A"],"seq_region_name":"7","id":"rs1214207494","clinical_significance":[]},{"start":140590351,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140590351,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1798963740","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140590354,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590354,"clinical_significance":[],"seq_region_name":"7","id":"rs1336911360"},{"end":140590355,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140590355,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs892481600","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140590358,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590358,"source":"dbSNP","seq_region_name":"7","id":"rs1246822514","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798964216","clinical_significance":[],"start":140590363,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140590363,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140590366,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590366,"source":"dbSNP","seq_region_name":"7","id":"rs1798964325","clinical_significance":[]},{"start":140590368,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140590368,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs180876405","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590369,"source":"dbSNP","strand":1,"feature_type":"variation","end":140590369,"alleles":["G","A"],"seq_region_name":"7","id":"rs982574025","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798964720","clinical_significance":[],"alleles":["GACAGAGAC","GAC"],"end":140590377,"strand":1,"feature_type":"variation","start":140590369,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140590376,"alleles":["AGAGA","AGA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140590372,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798964837"},{"seq_region_name":"7","id":"rs1389900298","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590375,"source":"dbSNP","strand":1,"feature_type":"variation","end":140590375,"alleles":["G","C"]},{"seq_region_name":"7","id":"rs1395801084","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590376,"source":"dbSNP","strand":1,"feature_type":"variation","end":140590376,"alleles":["A","G"]},{"feature_type":"variation","strand":1,"end":140590377,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590377,"clinical_significance":[],"id":"rs1487846987","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1326701037","clinical_significance":[],"strand":1,"feature_type":"variation","end":140590385,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590385,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585705377","alleles":["A","G"],"end":140590386,"feature_type":"variation","strand":1,"source":"dbSNP","start":140590386,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1798965764","seq_region_name":"7","source":"dbSNP","start":140590386,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AAAAAA","AAAAAAA"],"end":140590391,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1195907234","seq_region_name":"7","source":"dbSNP","start":140590391,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["ATACATACATACATA","ATACATACATACATACATA"],"end":140590405,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs912287307","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590392,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140590392},{"clinical_significance":[],"id":"rs1164657671","seq_region_name":"7","source":"dbSNP","start":140590395,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140590395,"alleles":["A","C"],"feature_type":"variation","strand":1},{"alleles":["T","C"],"end":140590396,"strand":1,"feature_type":"variation","start":140590396,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798966515","clinical_significance":[]},{"seq_region_name":"7","id":"rs943909458","clinical_significance":[],"alleles":["C","T"],"end":140590398,"strand":1,"feature_type":"variation","start":140590398,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1470680092","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140590406,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590406},{"strand":1,"feature_type":"variation","end":140590407,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590407,"source":"dbSNP","seq_region_name":"7","id":"rs1798967014","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590412,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140590412,"clinical_significance":[],"id":"rs1798967175","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs754275469","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140590415,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590415},{"id":"rs1365927446","seq_region_name":"7","clinical_significance":[],"start":140590418,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140590418,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs975217400","clinical_significance":[],"alleles":["T","A","C"],"end":140590419,"strand":1,"feature_type":"variation","start":140590419,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590420,"source":"dbSNP","strand":1,"feature_type":"variation","end":140590420,"alleles":["G","A"],"seq_region_name":"7","id":"rs1481856567","clinical_significance":[]},{"source":"dbSNP","start":140590424,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140590424,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1563162892"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798968303","end":140590425,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140590425,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140590428,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140590428,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1285443736","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1181084894","feature_type":"variation","strand":1,"end":140590430,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590430},{"seq_region_name":"7","id":"rs1411684757","clinical_significance":[],"alleles":["G","A"],"end":140590431,"strand":1,"feature_type":"variation","start":140590431,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1798969176","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590437,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140590437},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590444,"feature_type":"variation","strand":1,"end":140590444,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1046688715"},{"clinical_significance":[],"id":"rs1469751608","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590446,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140590446},{"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140590448,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590448,"source":"dbSNP","id":"rs1798969715","seq_region_name":"7","clinical_significance":[]},{"end":140590450,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140590450,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798969938","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798970114","clinical_significance":[],"end":140590453,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140590453,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590454,"feature_type":"variation","strand":1,"end":140590454,"alleles":["G","T"],"clinical_significance":[],"id":"rs2130657186","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1271264615","seq_region_name":"7","source":"dbSNP","start":140590463,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140590463,"alleles":["G","A"],"feature_type":"variation","strand":1},{"id":"rs2130657195","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590466,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140590466},{"feature_type":"variation","strand":1,"end":140590467,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590467,"clinical_significance":[],"seq_region_name":"7","id":"rs1798970491"},{"source":"dbSNP","start":140590473,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140590473,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798970676"},{"clinical_significance":[],"seq_region_name":"7","id":"rs543183818","source":"dbSNP","start":140590474,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140590474,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798971035","source":"dbSNP","start":140590476,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140590476,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1424763458","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590478,"feature_type":"variation","strand":1,"end":140590478,"alleles":["T","C","G"]},{"feature_type":"variation","strand":1,"end":140590481,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590481,"clinical_significance":[],"id":"rs1212994742","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140590488,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590488,"source":"dbSNP","seq_region_name":"7","id":"rs74492801","clinical_significance":[]},{"clinical_significance":[],"id":"rs2130657259","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140590489,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590489},{"end":140590490,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140590490,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1563162935","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590493,"source":"dbSNP","strand":1,"feature_type":"variation","end":140590493,"alleles":["T","C"],"seq_region_name":"7","id":"rs1798971989","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590497,"source":"dbSNP","strand":1,"feature_type":"variation","end":140590497,"alleles":["A","AA"],"seq_region_name":"7","id":"rs1262292319","clinical_significance":[]},{"source":"dbSNP","start":140590498,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","-"],"end":140590498,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs759939176","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1034297676","seq_region_name":"7","alleles":["C","T"],"end":140590502,"feature_type":"variation","strand":1,"source":"dbSNP","start":140590502,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140590503,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590503,"source":"dbSNP","seq_region_name":"7","id":"rs1304225284","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140590520,"alleles":["ATA","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590518,"clinical_significance":[],"seq_region_name":"7","id":"rs1443286295"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590519,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140590519,"seq_region_name":"7","id":"rs1368879254","clinical_significance":[]},{"id":"rs1798972945","seq_region_name":"7","clinical_significance":[],"end":140590520,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140590520,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798973045","end":140590531,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140590531,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1325754360","seq_region_name":"7","alleles":["T","C"],"end":140590535,"feature_type":"variation","strand":1,"source":"dbSNP","start":140590535,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140590536,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140590536,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798973266"},{"clinical_significance":[],"seq_region_name":"7","id":"rs188717342","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140590538,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590538},{"clinical_significance":[],"seq_region_name":"7","id":"rs894212566","alleles":["C","T"],"end":140590542,"feature_type":"variation","strand":1,"source":"dbSNP","start":140590542,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140590544,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590544,"clinical_significance":[],"seq_region_name":"7","id":"rs921059109"},{"clinical_significance":[],"id":"rs936600957","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140590546,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590546},{"start":140590549,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140590549,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1372539498","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798974172","source":"dbSNP","start":140590550,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140590550,"alleles":["T","C"],"feature_type":"variation","strand":1},{"end":140590560,"alleles":["C","A","G"],"strand":1,"feature_type":"variation","start":140590560,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1408213396","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590563,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140590563,"clinical_significance":[],"id":"rs1451153233","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798974649","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590566,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140590566},{"seq_region_name":"7","id":"rs1379367758","clinical_significance":[],"strand":1,"feature_type":"variation","end":140590569,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590569,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1798974886","clinical_significance":[],"start":140590572,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140590572,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1193705520","seq_region_name":"7","source":"dbSNP","start":140590574,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140590574,"alleles":["A","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs111779456","source":"dbSNP","start":140590579,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140590579,"alleles":["C","T"],"feature_type":"variation","strand":1},{"id":"rs1798975266","seq_region_name":"7","clinical_significance":[],"end":140590581,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140590581,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798975381","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590582,"feature_type":"variation","strand":1,"end":140590582,"alleles":["A","T"]},{"seq_region_name":"7","id":"rs1355795503","clinical_significance":[],"start":140590590,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140590590,"strand":1,"feature_type":"variation"},{"end":140590593,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140590593,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798975628","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590594,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140590594,"seq_region_name":"7","id":"rs1798975735","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140590595,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590595,"source":"dbSNP","seq_region_name":"7","id":"rs1798975840","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590600,"feature_type":"variation","strand":1,"end":140590600,"alleles":["C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1798975976"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798976084","feature_type":"variation","strand":1,"end":140590602,"alleles":["T","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590602},{"alleles":["C","T"],"end":140590605,"strand":1,"feature_type":"variation","start":140590605,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1397590138","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798976365","clinical_significance":[],"alleles":["G","A"],"end":140590607,"strand":1,"feature_type":"variation","start":140590607,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140590609,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140590609,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs893155918","seq_region_name":"7","clinical_significance":[]},{"end":140590612,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140590612,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs371524922"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140590613,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590613,"clinical_significance":[],"id":"rs1798976716","seq_region_name":"7"},{"source":"dbSNP","start":140590624,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140590624,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1310441908","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1798976934","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590629,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140590629},{"seq_region_name":"7","id":"rs2130657535","clinical_significance":[],"alleles":["T","C"],"end":140590630,"strand":1,"feature_type":"variation","start":140590630,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs2130657543","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590633,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140590633},{"end":140590638,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140590638,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798977035","clinical_significance":[]},{"start":140590639,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G","T"],"end":140590639,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585705797","clinical_significance":[]},{"id":"rs1585705805","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140590642,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590642,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1041838173","source":"dbSNP","start":140590643,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140590643,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140590650,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590650,"source":"dbSNP","seq_region_name":"7","id":"rs1321019500","clinical_significance":[]},{"clinical_significance":[],"id":"rs2130657582","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140590652,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590652},{"seq_region_name":"7","id":"rs2130657592","clinical_significance":[],"start":140590653,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140590653,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590654,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140590654,"id":"rs961697579","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590660,"feature_type":"variation","strand":1,"end":140590660,"alleles":["T","C"],"clinical_significance":[],"id":"rs1350210350","seq_region_name":"7"},{"start":140590663,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140590663,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1281224048","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs907278414","source":"dbSNP","start":140590664,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140590664,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140590665,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590665,"source":"dbSNP","seq_region_name":"7","id":"rs571925375","clinical_significance":[]},{"end":140590670,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140590670,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs954661591","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","A","G","T"],"end":140590671,"strand":1,"feature_type":"variation","start":140590671,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1339541063","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs112538263","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590672,"feature_type":"variation","strand":1,"end":140590672,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs894617513","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140590677,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590677,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590680,"source":"dbSNP","strand":1,"feature_type":"variation","end":140590680,"alleles":["C","A"],"seq_region_name":"7","id":"rs1483754634","clinical_significance":[]},{"source":"dbSNP","start":140590683,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140590683,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1173808936"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590692,"feature_type":"variation","strand":1,"end":140590692,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1798981068"},{"alleles":["C","G"],"end":140590696,"strand":1,"feature_type":"variation","start":140590696,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1798981239","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590698,"source":"dbSNP","strand":1,"feature_type":"variation","end":140590698,"alleles":["C","T"],"seq_region_name":"7","id":"rs936747594","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1392678005","feature_type":"variation","strand":1,"end":140590699,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590699},{"id":"rs989985794","seq_region_name":"7","clinical_significance":[],"start":140590702,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140590702,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1798981724","clinical_significance":[],"alleles":["AACTAAC","AACTAACTAAC"],"end":140590711,"strand":1,"feature_type":"variation","start":140590705,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140590706,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140590706,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs181454524","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590713,"source":"dbSNP","strand":1,"feature_type":"variation","end":140590713,"alleles":["A","G"],"id":"rs1798981971","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590717,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140590717,"clinical_significance":[],"seq_region_name":"7","id":"rs1798982082"},{"alleles":["G","A"],"end":140590729,"feature_type":"variation","strand":1,"source":"dbSNP","start":140590729,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1475687924","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1798982311","seq_region_name":"7","alleles":["G","A"],"end":140590730,"feature_type":"variation","strand":1,"source":"dbSNP","start":140590730,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1183993844","clinical_significance":[],"start":140590731,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140590731,"alleles":["G","A","T"],"strand":1,"feature_type":"variation"},{"alleles":["G","T"],"end":140590735,"strand":1,"feature_type":"variation","start":140590735,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs2130657762","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","C"],"end":140590739,"strand":1,"feature_type":"variation","start":140590739,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1798982586","clinical_significance":[]},{"seq_region_name":"7","id":"rs995774517","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590743,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140590743},{"source":"dbSNP","start":140590748,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140590748,"alleles":["T","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1423717130","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1027629796","clinical_significance":[],"strand":1,"feature_type":"variation","end":140590749,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590749,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590752,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140590752,"clinical_significance":[],"seq_region_name":"7","id":"rs569071575"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140590754,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590754,"clinical_significance":[],"seq_region_name":"7","id":"rs1798983205"},{"seq_region_name":"7","id":"rs1798983323","clinical_significance":[],"end":140590762,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140590762,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590768,"feature_type":"variation","strand":1,"end":140590768,"alleles":["A","T"],"clinical_significance":[],"id":"rs1798983434","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140590770,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590770,"clinical_significance":[],"id":"rs1798983552","seq_region_name":"7"},{"start":140590772,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140590772,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs951106340","clinical_significance":[]},{"clinical_significance":[],"id":"rs1487806491","seq_region_name":"7","source":"dbSNP","start":140590779,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140590779,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1798983900","clinical_significance":[],"end":140590783,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140590783,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1257995840","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590784,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140590784},{"source":"dbSNP","start":140590785,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A","C"],"end":140590785,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1213239747"},{"clinical_significance":[],"id":"rs982849240","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140590786,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590786},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590788,"source":"dbSNP","strand":1,"feature_type":"variation","end":140590788,"alleles":["C","T"],"id":"rs1798984402","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs536441926","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590793,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140590793},{"alleles":["CC","C"],"end":140590795,"feature_type":"variation","strand":1,"source":"dbSNP","start":140590794,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798984683"},{"source":"dbSNP","start":140590796,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140590796,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130657901"},{"start":140590797,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140590797,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130657912","clinical_significance":[]},{"alleles":["G","C"],"end":140590799,"strand":1,"feature_type":"variation","start":140590799,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs965105027","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130657925","clinical_significance":[],"alleles":["G","T"],"end":140590802,"strand":1,"feature_type":"variation","start":140590802,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140590807,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140590807,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798984904"},{"feature_type":"variation","strand":1,"end":140590815,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590815,"clinical_significance":[],"seq_region_name":"7","id":"rs975100659"},{"clinical_significance":[],"id":"rs945360904","seq_region_name":"7","source":"dbSNP","start":140590831,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140590831,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1215304866","source":"dbSNP","start":140590844,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140590844,"alleles":["G","C"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140590851,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140590851,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1342084071","seq_region_name":"7"},{"end":140590852,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140590852,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1392092409","clinical_significance":[]},{"alleles":["GAGAGAG","GAGAG"],"end":140590858,"strand":1,"feature_type":"variation","start":140590852,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1046470303","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798985797","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590854,"feature_type":"variation","strand":1,"end":140590854,"alleles":["G","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs928191818","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590856,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140590856},{"end":140590862,"alleles":["G","C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140590862,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798986029"},{"start":140590864,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140590864,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1356445246","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590875,"feature_type":"variation","strand":1,"end":140590875,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1798986308"},{"seq_region_name":"7","id":"rs921109889","clinical_significance":[],"strand":1,"feature_type":"variation","end":140590877,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590877,"source":"dbSNP"},{"source":"dbSNP","start":140590878,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140590878,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1798986567"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798986694","feature_type":"variation","strand":1,"end":140590881,"alleles":["AATA","AATAGTAATAATAATAATAATAATAATA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590878},{"end":140590886,"alleles":["AATAATAAT","AATAATAATTAATAATAATAATAATAATAATAATAAT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140590878,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1563163118"},{"clinical_significance":[],"seq_region_name":"7","id":"rs145861724","source":"dbSNP","start":140590878,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AATAATAATAATAATAA","AATAATAATAATAA","AATAATAATAATAATAATAA","AATAATAATAATAATAATAATAATAA","AATAATAATAATAATAATAATAATAATAA","AATAATAATAATAATAATAATAATAATAATAA","AATAATAATAATAATAATAATAATAATAATAATAA","AATAATAATAATAATAATAATAATAATAATAATAATAA","AATAATAATAATAATAATAATAATAATAATAATAATAATAA","AATAATAATAATAATAATAATAATAATAATAATAATAATAATAA","AATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAA"],"end":140590894,"feature_type":"variation","strand":1},{"end":140590882,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140590882,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1798987786","seq_region_name":"7"},{"end":140590885,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140590885,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs574100704","clinical_significance":[]},{"seq_region_name":"7","id":"rs1360002037","clinical_significance":[],"end":140590886,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140590886,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1798988430","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590886,"source":"dbSNP","strand":1,"feature_type":"variation","end":140590886,"alleles":["T","TT"]},{"start":140590891,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140590891,"alleles":["A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs938291510","clinical_significance":[]},{"seq_region_name":"7","id":"rs771703120","clinical_significance":[],"start":140590892,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140590892,"strand":1,"feature_type":"variation"},{"alleles":["A","T"],"end":140590893,"feature_type":"variation","strand":1,"source":"dbSNP","start":140590893,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1798989038"},{"strand":1,"feature_type":"variation","alleles":["AAAAAAAA","AAAAAAA","AAAAAAAAA","AAAAAAAAAAA"],"end":140590900,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590893,"source":"dbSNP","seq_region_name":"7","id":"rs1205500231","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs745453373","end":140590894,"alleles":["-","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140590895,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs111681678","end":140590895,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140590895,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140590896,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140590896,"alleles":["A","ATAATAATAATA","ATAATAATAATAATA","ATAATAATAATAATAATA","ATAATAATAATAATAATAATA","ATAATAATAATAATAATAATAATA","ATAATAATAATAATAATAATAATAATA","ATAATAATAATAATAATAATAATAATAATA","ATAATAATAATAATAATAATAATAATAATAATA"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs775140274"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798989793","alleles":["A","G"],"end":140590896,"feature_type":"variation","strand":1,"source":"dbSNP","start":140590896,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590901,"feature_type":"variation","strand":1,"end":140590901,"alleles":["G","A","T"],"clinical_significance":[],"id":"rs79623738","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1195687672","seq_region_name":"7","feature_type":"variation","strand":1,"end":140590902,"alleles":["GG","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590901},{"clinical_significance":[],"seq_region_name":"7","id":"rs1300843726","end":140590902,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140590902,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590903,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140590903,"clinical_significance":[],"id":"rs1378248316","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590904,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140590904,"id":"rs1798990792","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","G"],"end":140590916,"feature_type":"variation","strand":1,"source":"dbSNP","start":140590916,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs78286958"},{"start":140590923,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140590923,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1295474436","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798991181","clinical_significance":[],"alleles":["C","T"],"end":140590931,"strand":1,"feature_type":"variation","start":140590931,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1005939903","source":"dbSNP","start":140590932,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140590932,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140590935,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590935,"clinical_significance":[],"seq_region_name":"7","id":"rs1353175800"},{"start":140590940,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C"],"end":140590940,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs145073167","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798991738","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590941,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140590941},{"feature_type":"variation","strand":1,"end":140590953,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140590953,"clinical_significance":[],"seq_region_name":"7","id":"rs946106365"},{"alleles":["A","G"],"end":140590954,"feature_type":"variation","strand":1,"source":"dbSNP","start":140590954,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585706445"},{"seq_region_name":"7","id":"rs1042113291","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140590955,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590955,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1299737961","alleles":["T","C","G"],"end":140590960,"feature_type":"variation","strand":1,"source":"dbSNP","start":140590960,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["A","C"],"end":140590965,"feature_type":"variation","strand":1,"source":"dbSNP","start":140590965,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1326328378"},{"seq_region_name":"7","id":"rs1798992551","clinical_significance":[],"end":140590970,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140590970,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140590978,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140590981,"alleles":["AAAA","AAAAA"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1465020642"},{"seq_region_name":"7","id":"rs1563163211","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590982,"source":"dbSNP","strand":1,"feature_type":"variation","end":140590982,"alleles":["C","T"]},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140590983,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140590983,"source":"dbSNP","seq_region_name":"7","id":"rs1395206575","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585706528","clinical_significance":[],"alleles":["A","T"],"end":140590987,"strand":1,"feature_type":"variation","start":140590987,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140590991,"alleles":["AAAAA","AAAAAAA"],"strand":1,"feature_type":"variation","start":140590987,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1037859002","clinical_significance":[]},{"clinical_significance":[],"id":"rs928586122","seq_region_name":"7","alleles":["A","G"],"end":140590988,"feature_type":"variation","strand":1,"source":"dbSNP","start":140590988,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1563163230","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591000,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AAAAAAA","AAAAAA"],"end":140591006},{"seq_region_name":"7","id":"rs1227056297","clinical_significance":[],"end":140591014,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140591014,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1362322697","clinical_significance":[],"alleles":["GGGGG","GGGG"],"end":140591018,"strand":1,"feature_type":"variation","start":140591014,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591015,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140591015,"seq_region_name":"7","id":"rs897619670","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs938759414","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591016,"feature_type":"variation","strand":1,"end":140591016,"alleles":["G","A","T"]},{"seq_region_name":"7","id":"rs2130658347","clinical_significance":[],"start":140591018,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140591018,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591019,"source":"dbSNP","strand":1,"feature_type":"variation","end":140591019,"alleles":["T","C"],"seq_region_name":"7","id":"rs1471296896","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140591020,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591020,"source":"dbSNP","seq_region_name":"7","id":"rs1798994076","clinical_significance":[]},{"seq_region_name":"7","id":"rs552663928","clinical_significance":[],"start":140591023,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140591023,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs993116442","source":"dbSNP","start":140591024,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140591024,"feature_type":"variation","strand":1},{"end":140591027,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140591027,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1469293316","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140591031,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591031,"source":"dbSNP","seq_region_name":"7","id":"rs1029981989","clinical_significance":[]},{"seq_region_name":"7","id":"rs112372283","clinical_significance":[],"end":140591035,"alleles":["C","A","G"],"strand":1,"feature_type":"variation","start":140591035,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1321448489","clinical_significance":[],"strand":1,"feature_type":"variation","end":140591036,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591036,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1254612339","end":140591038,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140591038,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798995084","end":140591045,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140591045,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1585706650","seq_region_name":"7","feature_type":"variation","strand":1,"end":140591047,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591047},{"feature_type":"variation","strand":1,"end":140591048,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591048,"clinical_significance":[],"seq_region_name":"7","id":"rs1798995385"},{"strand":1,"feature_type":"variation","end":140591049,"alleles":["G","C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591049,"source":"dbSNP","seq_region_name":"7","id":"rs1798995515","clinical_significance":[]},{"seq_region_name":"7","id":"rs1007909161","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591050,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140591050},{"clinical_significance":[],"seq_region_name":"7","id":"rs760238294","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591052,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140591052},{"seq_region_name":"7","id":"rs1585706675","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140591055,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591055,"source":"dbSNP"},{"seq_region_name":"7","id":"rs528607069","clinical_significance":[],"alleles":["G","A"],"end":140591056,"strand":1,"feature_type":"variation","start":140591056,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140591056,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140591058,"alleles":["GGG","GG"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs2130658474","seq_region_name":"7"},{"start":140591057,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140591057,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs111912602","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1445489078","end":140591060,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140591060,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591063,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140591063,"clinical_significance":[],"seq_region_name":"7","id":"rs1048675772"},{"id":"rs1327774874","seq_region_name":"7","clinical_significance":[],"end":140591064,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140591064,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798996757","feature_type":"variation","strand":1,"alleles":["GGTGGACTGCTTGAGCT","-"],"end":140591086,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591070},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140591071,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591071,"source":"dbSNP","id":"rs1585706750","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140591079,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140591079,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs887356576"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798997102","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591081,"feature_type":"variation","strand":1,"end":140591081,"alleles":["T","A"]},{"seq_region_name":"7","id":"rs1798997226","clinical_significance":[],"end":140591082,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140591082,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140591085,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140591085,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1004431390"},{"seq_region_name":"7","id":"rs1349046250","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591090,"source":"dbSNP","strand":1,"feature_type":"variation","end":140591090,"alleles":["G","A"]},{"start":140591092,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140591092,"strand":1,"feature_type":"variation","id":"rs1798997825","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1798998004","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591099,"source":"dbSNP","strand":1,"feature_type":"variation","end":140591099,"alleles":["A","C"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591100,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140591100,"seq_region_name":"7","id":"rs776258569","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140591101,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591101,"source":"dbSNP","seq_region_name":"7","id":"rs112579682","clinical_significance":[]},{"alleles":["A","G"],"end":140591102,"feature_type":"variation","strand":1,"source":"dbSNP","start":140591102,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1798998590","seq_region_name":"7"},{"alleles":["GGG","GG"],"end":140591108,"strand":1,"feature_type":"variation","start":140591106,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1406132882","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1158118577","feature_type":"variation","strand":1,"end":140591109,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591109},{"clinical_significance":[],"seq_region_name":"7","id":"rs1798999012","source":"dbSNP","start":140591110,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140591110,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591114,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140591114,"seq_region_name":"7","id":"rs1798999142","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140591116,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591116,"clinical_significance":[],"seq_region_name":"7","id":"rs1435117089"},{"end":140591121,"alleles":["A","C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140591121,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1454715614"},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140591122,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591122,"clinical_significance":[],"seq_region_name":"7","id":"rs1798999568"},{"clinical_significance":[],"id":"rs1798999698","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591123,"feature_type":"variation","strand":1,"end":140591123,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1254988783","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591126,"source":"dbSNP","strand":1,"feature_type":"variation","end":140591126,"alleles":["G","A"]},{"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140591127,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591127,"clinical_significance":[],"seq_region_name":"7","id":"rs2130658651"},{"seq_region_name":"7","id":"rs1192261652","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591132,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140591132},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591133,"source":"dbSNP","strand":1,"feature_type":"variation","end":140591133,"alleles":["T","A","C"],"seq_region_name":"7","id":"rs1243035370","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591135,"source":"dbSNP","strand":1,"feature_type":"variation","end":140591135,"alleles":["A","T"],"seq_region_name":"7","id":"rs113344755","clinical_significance":[]},{"start":140591138,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140591138,"alleles":["G","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130658678","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591140,"feature_type":"variation","strand":1,"end":140591140,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799000383"},{"seq_region_name":"7","id":"rs1028012461","clinical_significance":[],"alleles":["C","T"],"end":140591142,"strand":1,"feature_type":"variation","start":140591142,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1318351967","clinical_significance":[],"alleles":["A","C"],"end":140591144,"strand":1,"feature_type":"variation","start":140591144,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140591153,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140591153,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799000623","clinical_significance":[]},{"alleles":["G","A","C"],"end":140591154,"strand":1,"feature_type":"variation","start":140591154,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs957895860","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799000891","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591156,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140591156},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799001022","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140591159,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591159},{"clinical_significance":[],"id":"rs542822894","seq_region_name":"7","alleles":["C","T"],"end":140591167,"feature_type":"variation","strand":1,"source":"dbSNP","start":140591167,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1799001258","clinical_significance":[],"strand":1,"feature_type":"variation","end":140591169,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591169,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140591171,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591171,"source":"dbSNP","id":"rs750912707","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591174,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140591174,"clinical_significance":[],"seq_region_name":"7","id":"rs927974315"},{"end":140591175,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140591175,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799001623"},{"strand":1,"feature_type":"variation","end":140591177,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591177,"source":"dbSNP","seq_region_name":"7","id":"rs561467000","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591178,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140591178,"seq_region_name":"7","id":"rs1386397182","clinical_significance":[]},{"start":140591191,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140591191,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799001975","clinical_significance":[]},{"end":140591192,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140591192,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1783986458","clinical_significance":[]},{"source":"dbSNP","start":140591193,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140591193,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1055797571"},{"id":"rs7456177","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140591196,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591196,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1799002349","seq_region_name":"7","feature_type":"variation","strand":1,"end":140591198,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591198},{"strand":1,"feature_type":"variation","end":140591200,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591200,"source":"dbSNP","id":"rs1799002473","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1343219943","alleles":["G","A"],"end":140591203,"feature_type":"variation","strand":1,"source":"dbSNP","start":140591203,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs528544309","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591205,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140591205},{"id":"rs910013313","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591207,"source":"dbSNP","strand":1,"feature_type":"variation","end":140591207,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs913694787","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591208,"feature_type":"variation","strand":1,"end":140591208,"alleles":["G","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1274899880","source":"dbSNP","start":140591212,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140591212,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs941523151","end":140591216,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140591216,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140591220,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591220,"source":"dbSNP","id":"rs1799003306","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs185744382","clinical_significance":[],"end":140591222,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140591222,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1217107575","seq_region_name":"7","clinical_significance":[],"start":140591227,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140591227,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140591228,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591228,"clinical_significance":[],"id":"rs758959588","seq_region_name":"7"},{"alleles":["G","A"],"end":140591229,"strand":1,"feature_type":"variation","start":140591229,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs766589329","clinical_significance":[]},{"end":140591230,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140591230,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1188809742","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140591231,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591231,"clinical_significance":[],"id":"rs1485066331","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1300167338","seq_region_name":"7","source":"dbSNP","start":140591232,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140591232,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs868374014","source":"dbSNP","start":140591237,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140591237,"alleles":["C","T"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140591238,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591238,"clinical_significance":[],"seq_region_name":"7","id":"rs1563163399"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591242,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140591242,"clinical_significance":[],"seq_region_name":"7","id":"rs1311930942"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591247,"feature_type":"variation","strand":1,"end":140591247,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799004692"},{"source":"dbSNP","start":140591248,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140591248,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799004803"},{"source":"dbSNP","start":140591256,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140591278,"alleles":["CACTGCATTCCAGCCACTGCACT","CACT"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799004961"},{"seq_region_name":"7","id":"rs1037196188","clinical_significance":[],"strand":1,"feature_type":"variation","end":140591258,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591258,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799005205","end":140591259,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140591259,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799005321","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591263,"feature_type":"variation","strand":1,"end":140591263,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1799005466","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591264,"source":"dbSNP","strand":1,"feature_type":"variation","end":140591279,"alleles":["TCCAGCCACTGCACTC","TCCAGCCACTGCACTCCAGCCACTGCACTC"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591265,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140591265,"clinical_significance":[],"seq_region_name":"7","id":"rs1799005583"},{"clinical_significance":[],"seq_region_name":"7","id":"rs141508008","source":"dbSNP","start":140591266,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140591266,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130658983","end":140591269,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140591269,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140591273,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140591273,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs532677520","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140591276,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591276,"source":"dbSNP","seq_region_name":"7","id":"rs112349892","clinical_significance":[]},{"seq_region_name":"7","id":"rs915987627","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140591277,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591277,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140591281,"alleles":["CTCTC","CTC"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591277,"clinical_significance":[],"seq_region_name":"7","id":"rs1799006457"},{"seq_region_name":"7","id":"rs931539376","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140591283,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591283,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130659033","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591284,"feature_type":"variation","strand":1,"end":140591284,"alleles":["T","C"]},{"end":140591290,"alleles":["TTTT","T"],"strand":1,"feature_type":"variation","start":140591287,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1247361637","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799006885","source":"dbSNP","start":140591290,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140591290,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140591294,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591294,"source":"dbSNP","seq_region_name":"7","id":"rs1585707237","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591295,"feature_type":"variation","strand":1,"end":140591295,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1049043960"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591297,"feature_type":"variation","strand":1,"alleles":["GAGTGAG","GAG"],"end":140591303,"clinical_significance":[],"seq_region_name":"7","id":"rs1297400044"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591300,"feature_type":"variation","strand":1,"end":140591300,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs887252167"},{"alleles":["G","A"],"end":140591301,"feature_type":"variation","strand":1,"source":"dbSNP","start":140591301,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799007361"},{"start":140591301,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["GAGA","GAGAGA"],"end":140591304,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799007462","clinical_significance":[]},{"alleles":["C","A"],"end":140591305,"feature_type":"variation","strand":1,"source":"dbSNP","start":140591305,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799007576"},{"seq_region_name":"7","id":"rs1377566064","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591306,"source":"dbSNP","strand":1,"feature_type":"variation","end":140591306,"alleles":["C","A"]},{"start":140591307,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140591307,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1489509361","clinical_significance":[]},{"alleles":["A","G"],"end":140591315,"strand":1,"feature_type":"variation","start":140591315,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1051356963","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591316,"feature_type":"variation","strand":1,"end":140591316,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1465553369"},{"start":140591317,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140591317,"alleles":["A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799008225","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591317,"feature_type":"variation","strand":1,"alleles":["ATA","A"],"end":140591319,"clinical_significance":[],"seq_region_name":"7","id":"rs1355202561"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591318,"feature_type":"variation","strand":1,"alleles":["T","-"],"end":140591318,"clinical_significance":[],"seq_region_name":"7","id":"rs1799008478"},{"feature_type":"variation","strand":1,"end":140591322,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591322,"clinical_significance":[],"seq_region_name":"7","id":"rs2130659130"},{"seq_region_name":"7","id":"rs1173108597","clinical_significance":[],"start":140591323,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140591323,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1654526021","clinical_significance":[],"start":140591323,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140591323,"alleles":["G","-"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1427287688","source":"dbSNP","start":140591325,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140591325,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591326,"source":"dbSNP","strand":1,"feature_type":"variation","end":140591326,"alleles":["G","C"],"seq_region_name":"7","id":"rs1423313892","clinical_significance":[]},{"seq_region_name":"7","id":"rs113057709","clinical_significance":[],"strand":1,"feature_type":"variation","end":140591327,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591327,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1475321353","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591328,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140591328},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140591330,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591330,"clinical_significance":[],"seq_region_name":"7","id":"rs2130659186"},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140591333,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591333,"source":"dbSNP","seq_region_name":"7","id":"rs1799009109","clinical_significance":[]},{"clinical_significance":[],"id":"rs781445301","seq_region_name":"7","feature_type":"variation","strand":1,"end":140591335,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591335},{"seq_region_name":"7","id":"rs1799009370","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140591336,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591336,"source":"dbSNP"},{"seq_region_name":"7","id":"rs115390407","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591337,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140591337},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591337,"source":"dbSNP","strand":1,"feature_type":"variation","end":140591358,"alleles":["TTGCAAAACTAATTTGCAAAAC","TTGCAAAACTAATTTGCAAAACTAATTTGCAAAAC"],"seq_region_name":"7","id":"rs1259261322","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591338,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140591338,"clinical_significance":[],"seq_region_name":"7","id":"rs1799009750"},{"seq_region_name":"7","id":"rs900870576","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591340,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140591340},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591341,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140591341,"seq_region_name":"7","id":"rs1799009987","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799010110","end":140591344,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140591344,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1482610947","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591346,"feature_type":"variation","strand":1,"end":140591346,"alleles":["T","C","G"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591349,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140591349,"clinical_significance":[],"id":"rs1799010403","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799010517","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591351,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140591351},{"id":"rs1472771913","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140591354,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591354,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591358,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140591358,"clinical_significance":[],"seq_region_name":"7","id":"rs370885404"},{"source":"dbSNP","start":140591359,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140591359,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs548456354"},{"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140591364,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591364,"source":"dbSNP","id":"rs1799011061","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591367,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140591367,"clinical_significance":[],"id":"rs1799011186","seq_region_name":"7"},{"source":"dbSNP","start":140591367,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140591370,"alleles":["AAAA","AAA"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1456625159","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1585707481","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140591369,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591369,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140591371,"alleles":["G","C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591371,"source":"dbSNP","seq_region_name":"7","id":"rs1028064815","clinical_significance":[]},{"alleles":["G","T"],"end":140591372,"feature_type":"variation","strand":1,"source":"dbSNP","start":140591372,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs957784830"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1010621058","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140591376,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591376},{"id":"rs138306159","seq_region_name":"7","clinical_significance":[],"start":140591377,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140591377,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140591385,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591385,"source":"dbSNP","seq_region_name":"7","id":"rs1799012307","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591387,"source":"dbSNP","strand":1,"feature_type":"variation","end":140591387,"alleles":["G","A"],"id":"rs1799012429","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1310778760","clinical_significance":[],"strand":1,"feature_type":"variation","end":140591392,"alleles":["A","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591392,"source":"dbSNP"},{"source":"dbSNP","start":140591394,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140591394,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799012682","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140591396,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591396,"clinical_significance":[],"seq_region_name":"7","id":"rs1351046529"},{"clinical_significance":[],"id":"rs1799012923","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140591402,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591402},{"feature_type":"variation","strand":1,"end":140591403,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591403,"clinical_significance":[],"seq_region_name":"7","id":"rs1799013170"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1011146197","end":140591408,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140591408,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1020826723","source":"dbSNP","start":140591420,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["GG","G"],"end":140591421,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1799013789","seq_region_name":"7","source":"dbSNP","start":140591437,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140591437,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1433709099","clinical_significance":[],"strand":1,"feature_type":"variation","end":140591440,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591440,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140591441,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591441,"clinical_significance":[],"id":"rs1464497739","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591442,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140591442,"seq_region_name":"7","id":"rs966766452","clinical_significance":[]},{"seq_region_name":"7","id":"rs144141452","clinical_significance":[],"alleles":["C","G","T"],"end":140591457,"strand":1,"feature_type":"variation","start":140591457,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140591459,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140591459,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs959642999","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140591465,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591465,"clinical_significance":[],"id":"rs2130659445","seq_region_name":"7"},{"alleles":["A","G"],"end":140591466,"feature_type":"variation","strand":1,"source":"dbSNP","start":140591466,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799014914"},{"end":140591467,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","start":140591467,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs982458707","clinical_significance":[]},{"seq_region_name":"7","id":"rs1034920959","clinical_significance":[],"strand":1,"feature_type":"variation","end":140591470,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591470,"source":"dbSNP"},{"seq_region_name":"7","id":"rs2130659482","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591474,"source":"dbSNP","strand":1,"feature_type":"variation","end":140591474,"alleles":["C","T"]},{"source":"dbSNP","start":140591477,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140591477,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1416160809"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799015372","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591480,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140591480},{"seq_region_name":"7","id":"rs1229906116","clinical_significance":[],"strand":1,"feature_type":"variation","end":140591483,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591483,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1290587432","feature_type":"variation","strand":1,"end":140591488,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591488},{"strand":1,"feature_type":"variation","end":140591491,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591491,"source":"dbSNP","seq_region_name":"7","id":"rs1799015731","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799015860","clinical_significance":[],"strand":1,"feature_type":"variation","end":140591495,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591495,"source":"dbSNP"},{"alleles":["AA","A"],"end":140591497,"feature_type":"variation","strand":1,"source":"dbSNP","start":140591496,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799015985","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1422921105","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591498,"source":"dbSNP","strand":1,"feature_type":"variation","end":140591498,"alleles":["G","C"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591499,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140591499,"clinical_significance":[],"seq_region_name":"7","id":"rs960061226"},{"id":"rs1799016342","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591507,"source":"dbSNP","strand":1,"feature_type":"variation","end":140591507,"alleles":["C","A"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591508,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140591508,"id":"rs1799016464","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130659579","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591511,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140591511},{"alleles":["T","A"],"end":140591514,"strand":1,"feature_type":"variation","start":140591514,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799016571","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1327610720","alleles":["T","A","C"],"end":140591525,"feature_type":"variation","strand":1,"source":"dbSNP","start":140591525,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140591533,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591533,"source":"dbSNP","seq_region_name":"7","id":"rs1250589543","clinical_significance":[]},{"alleles":["G","A"],"end":140591536,"strand":1,"feature_type":"variation","start":140591536,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs79887155","clinical_significance":[]},{"id":"rs777841985","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591538,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140591538},{"clinical_significance":[],"seq_region_name":"7","id":"rs1456384431","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140591550,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591550},{"start":140591551,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140591551,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130659626","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140591552,"alleles":["A","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591552,"clinical_significance":[],"seq_region_name":"7","id":"rs1799017358"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799017506","alleles":["C","T"],"end":140591559,"feature_type":"variation","strand":1,"source":"dbSNP","start":140591559,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["A","G"],"end":140591560,"strand":1,"feature_type":"variation","start":140591560,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1257274003","clinical_significance":[]},{"id":"rs915876356","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591565,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140591565},{"id":"rs1214262091","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591566,"source":"dbSNP","strand":1,"feature_type":"variation","end":140591566,"alleles":["T","A","C"]},{"start":140591569,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140591569,"alleles":["A","G"],"strand":1,"feature_type":"variation","id":"rs1336619722","seq_region_name":"7","clinical_significance":[]},{"end":140591570,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140591570,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1263492201","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799018243","end":140591571,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140591571,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140591578,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140591578,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799018355"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1244288277","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591579,"feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140591579},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591582,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140591582,"seq_region_name":"7","id":"rs1309216612","clinical_significance":[]},{"end":140591590,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140591590,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs745722759"},{"strand":1,"feature_type":"variation","end":140591594,"alleles":["T","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591594,"source":"dbSNP","seq_region_name":"7","id":"rs772112580","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs931399343","source":"dbSNP","start":140591595,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140591595,"alleles":["G","A","C"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140591596,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591596,"clinical_significance":[],"seq_region_name":"7","id":"rs1799019158"},{"end":140591603,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140591603,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1799019258","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs941651605","clinical_significance":[],"start":140591606,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140591606,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs571194938","clinical_significance":[],"alleles":["A","C","G"],"end":140591610,"strand":1,"feature_type":"variation","start":140591610,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs908722796","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591616,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140591616},{"seq_region_name":"7","id":"rs190553116","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140591618,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591618,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591623,"source":"dbSNP","strand":1,"feature_type":"variation","end":140591623,"alleles":["C","T"],"seq_region_name":"7","id":"rs1563163651","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799020134","clinical_significance":[],"strand":1,"feature_type":"variation","end":140591626,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591626,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591627,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140591627,"seq_region_name":"7","id":"rs1799020247","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799020429","source":"dbSNP","start":140591630,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TTCTTT","TT"],"end":140591635,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140591637,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TTTT","TTT"],"end":140591640,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1163088760","seq_region_name":"7"},{"source":"dbSNP","start":140591641,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140591641,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130659821"},{"end":140591645,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140591645,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs557320780"},{"start":140591646,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140591646,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1041310780","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799021197","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591646,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","CATTC"],"end":140591646},{"seq_region_name":"7","id":"rs151123012","clinical_significance":[],"end":140591657,"alleles":["CCTTCCTTCCTT","CCTT","CCTTCCTT","CCTTCCTTCCTTCCTT","CCTTCCTTCCTTCCTTCCTT"],"strand":1,"feature_type":"variation","start":140591646,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591649,"feature_type":"variation","strand":1,"end":140591649,"alleles":["T","C"],"clinical_significance":[],"id":"rs972856621","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs901426371","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591650,"feature_type":"variation","strand":1,"end":140591650,"alleles":["C","T"]},{"start":140591651,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140591651,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799022204","clinical_significance":[]},{"seq_region_name":"7","id":"rs1194137094","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["CTT","CTTTCTT"],"end":140591653,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591651,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591651,"source":"dbSNP","strand":1,"feature_type":"variation","end":140591675,"alleles":["CTTCCTTTCTTTCTTTCTTTCTCTT","CTT"],"seq_region_name":"7","id":"rs952277864","clinical_significance":[]},{"source":"dbSNP","start":140591652,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TT","T"],"end":140591653,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1209083808"},{"clinical_significance":[],"seq_region_name":"7","id":"rs76831022","source":"dbSNP","start":140591654,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140591654,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1799022994","seq_region_name":"7","end":140591671,"alleles":["CCTTTCTTTCTTTCTTTC","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140591654,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140591655,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["CTT","CTTCCTTTCTT"],"end":140591657,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799023170","clinical_significance":[]},{"clinical_significance":[],"id":"rs201214317","seq_region_name":"7","source":"dbSNP","start":140591655,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140591672,"alleles":["CTTTCTTTCTTTCTTTCT","CTTTCTTTCTTTCT","CTTTCTTTCTTTCTTTCTTTCT"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1799023661","clinical_significance":[],"start":140591655,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["CTTTCTTTCTTTCTTTCTCTTTCTTTCTTTCTTTCT","CTTTCTTTCTTTCTTTCT"],"end":140591690,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140591655,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["CTTTCTTTCTTTCTTTCTCTTTCTTTCTTTCTTTCTTTC","CTTTCTTTCTTTCTTTC"],"end":140591693,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799023839"},{"alleles":["T","C"],"end":140591658,"strand":1,"feature_type":"variation","start":140591658,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs536468114","clinical_significance":[]},{"seq_region_name":"7","id":"rs1483491144","clinical_significance":[],"start":140591658,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TCTTTCTTTCTTTCTCTTTCTTTCTTTCT","TCTTTCTTTCTTTCT"],"end":140591686,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591659,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140591659,"seq_region_name":"7","id":"rs1799024355","clinical_significance":[]},{"source":"dbSNP","start":140591660,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TTT","T"],"end":140591662,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799024508"},{"source":"dbSNP","start":140591660,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140591662,"alleles":["TTT","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799024620","seq_region_name":"7"},{"source":"dbSNP","start":140591660,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140591666,"alleles":["TTTCTTT","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1237114361"},{"feature_type":"variation","strand":1,"end":140591662,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591662,"clinical_significance":[],"seq_region_name":"7","id":"rs1051469308"},{"alleles":["TCT","T"],"end":140591664,"feature_type":"variation","strand":1,"source":"dbSNP","start":140591662,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799024964"},{"seq_region_name":"7","id":"rs1249340689","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591662,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TCTTTCTTTCTCTTTCTTTCT","TCTTTCTTTCT"],"end":140591682},{"source":"dbSNP","start":140591663,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140591663,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799025196"},{"source":"dbSNP","start":140591663,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140591663,"alleles":["C","CC"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130660019"},{"clinical_significance":[],"seq_region_name":"7","id":"rs758815559","source":"dbSNP","start":140591663,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["CTT","CTTCCTT"],"end":140591665,"feature_type":"variation","strand":1},{"id":"rs139489815","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591666,"source":"dbSNP","strand":1,"feature_type":"variation","end":140591666,"alleles":["T","C"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591666,"feature_type":"variation","strand":1,"alleles":["TCT","T","TCTCT"],"end":140591668,"clinical_significance":[],"seq_region_name":"7","id":"rs1383061677"},{"alleles":["TCTTTCTCTTTCT","TCTTTCT"],"end":140591678,"strand":1,"feature_type":"variation","start":140591666,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1415917161","seq_region_name":"7","clinical_significance":[]},{"end":140591667,"alleles":["C","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140591667,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1417513827"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591667,"source":"dbSNP","strand":1,"feature_type":"variation","end":140591667,"alleles":["C","T"],"seq_region_name":"7","id":"rs1799025767","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140591676,"alleles":["TTTCTCTTT","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591668,"source":"dbSNP","seq_region_name":"7","id":"rs1379114102","clinical_significance":[]},{"end":140591669,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140591669,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs370234873","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs796929191","end":140591671,"alleles":["TTC","CTT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140591669,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["TCTCT","T","TCT"],"end":140591674,"strand":1,"feature_type":"variation","start":140591670,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1478963135","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs374496615","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140591671,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591671},{"end":140591671,"alleles":["-","CT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140591672,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799026904"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1375928954","alleles":["T","TT","TTT","TTTCTCTTT","TTTCTTT","TTTCTTTCTTT","TTTCTTTCTTTCTTT","TTTCTTTCTTTCTTTCTTT"],"end":140591672,"feature_type":"variation","strand":1,"source":"dbSNP","start":140591672,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799027082","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591672,"feature_type":"variation","strand":1,"end":140591672,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1228818632","clinical_significance":[],"alleles":["TCTT","T"],"end":140591675,"strand":1,"feature_type":"variation","start":140591672,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs890090370","clinical_significance":[],"end":140591693,"alleles":["TCTTTCTTTCTTTCTTTCTTTC","TCTTTC","TCTTTCTTTCTTTC","TCTTTCTTTCTTTCTTTC","TCTTTCTTTCTTTCTTTCTTTCTTTC","TCTTTCTTTCTTTCTTTCTTTCTTTCTCTTTCTTTCTTTCTTTCTTTCTTTC","TCTTTCTTTCTTTCTTTCTTTCTTTCTTTC","TCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTC","TCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTC","TCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTC","TCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTC","TCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTC","TCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTC"],"strand":1,"feature_type":"variation","start":140591672,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1370701414","seq_region_name":"7","end":140591673,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140591673,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["T","C"],"end":140591674,"feature_type":"variation","strand":1,"source":"dbSNP","start":140591674,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs866411247"},{"id":"rs1491448318","seq_region_name":"7","clinical_significance":[],"start":140591674,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140591676,"alleles":["TTT","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1563163774","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591674,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TTTCTTT","T"],"end":140591680},{"seq_region_name":"7","id":"rs1436917927","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140591675,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591675,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591676,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140591676,"clinical_significance":[],"seq_region_name":"7","id":"rs1585708218"},{"end":140591678,"alleles":["TCT","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140591676,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs763298011"},{"clinical_significance":[],"seq_region_name":"7","id":"rs866767585","alleles":["T","C"],"end":140591678,"feature_type":"variation","strand":1,"source":"dbSNP","start":140591678,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140591680,"alleles":["TTT","TTTATTT","TTTT","TTTTT"],"strand":1,"feature_type":"variation","start":140591678,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs893699687","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591679,"feature_type":"variation","strand":1,"end":140591679,"alleles":["T","TCCTTTCCT"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799029492"},{"seq_region_name":"7","id":"rs1563163801","clinical_significance":[],"alleles":["TTC","TTCCTTC"],"end":140591681,"strand":1,"feature_type":"variation","start":140591679,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs745312474","seq_region_name":"7","source":"dbSNP","start":140591679,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140591685,"alleles":["TTCTTTC","TTCTTTCCTTCTTTC"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140591679,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140591689,"alleles":["TTCTTTCTTTC","TTCTTTCTTTCCTTCTTTCTTTC"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799029858"},{"id":"rs1348955415","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["TCT","T"],"end":140591682,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591680,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1477615391","clinical_significance":[],"alleles":["T","C"],"end":140591682,"strand":1,"feature_type":"variation","start":140591682,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140591684,"alleles":["TTT","TTTTT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591682,"source":"dbSNP","seq_region_name":"7","id":"rs1799030400","clinical_significance":[]},{"start":140591683,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140591685,"alleles":["TTC","TTCCTTC"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1563163816","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1010852040","source":"dbSNP","start":140591683,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140591687,"alleles":["TTCTT","TT"],"feature_type":"variation","strand":1},{"id":"rs1441963417","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591684,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TCT","T"],"end":140591686},{"end":140591685,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140591685,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799030917"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1440722231","source":"dbSNP","start":140591686,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140591685,"alleles":["-","CTTCTT"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1799031134","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140591686,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591686,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140591688,"alleles":["TTT","T","TTTT","TTTTT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591686,"clinical_significance":[],"seq_region_name":"7","id":"rs1799031250"},{"clinical_significance":[],"id":"rs1278040739","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140591688,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591688},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591688,"feature_type":"variation","strand":1,"alleles":["TCT","T","TCTCT"],"end":140591690,"clinical_significance":[],"seq_region_name":"7","id":"rs1585708308"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591689,"feature_type":"variation","strand":1,"end":140591689,"alleles":["C","CC"],"clinical_significance":[],"id":"rs1799031667","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130660368","source":"dbSNP","start":140591689,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140591689,"alleles":["C","A"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140591690,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140591690,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs560925369"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799031971","alleles":["T","TCCT"],"end":140591691,"feature_type":"variation","strand":1,"source":"dbSNP","start":140591691,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140591691,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TTC","TTCTTTCCTTC"],"end":140591693,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1554475937"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591691,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TTCCTTCCTTCCTTCCTTC","TTCCTTCCTTCCTTC","TTCCTTCCTTCCTTCCTTCCTTC"],"end":140591709,"id":"rs34439635","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","CTTCC"],"end":140591693,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591693,"clinical_significance":[],"seq_region_name":"7","id":"rs1563163849"},{"feature_type":"variation","strand":1,"end":140591694,"alleles":["CC","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591693,"clinical_significance":[],"seq_region_name":"7","id":"rs1356514497"},{"clinical_significance":[],"id":"rs201564565","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591694,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140591694},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799032787","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591695,"feature_type":"variation","strand":1,"end":140591694,"alleles":["-","CTTCTTTCTTTCTTTCT"]},{"strand":1,"feature_type":"variation","end":140591695,"alleles":["T","TCTT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591695,"source":"dbSNP","seq_region_name":"7","id":"rs1799032909","clinical_significance":[]},{"start":140591695,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140591696,"alleles":["TT","TTT","TTTCTTTCTTT"],"strand":1,"feature_type":"variation","id":"rs1799033050","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1563163862","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["TTC","TTCTTTCTTTCTTTCTTTC"],"end":140591697,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591695},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591696,"feature_type":"variation","strand":1,"end":140591696,"alleles":["T","A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs540329407"},{"end":140591697,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140591697,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs990703093","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140591698,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140591698,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs565372998","seq_region_name":"7"},{"alleles":["C","T"],"end":140591702,"strand":1,"feature_type":"variation","start":140591702,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs576876001","clinical_significance":[]},{"end":140591703,"alleles":["T","C","G"],"strand":1,"feature_type":"variation","start":140591703,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1410443495","seq_region_name":"7","clinical_significance":[]},{"start":140591706,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140591706,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs868596894","clinical_significance":[]},{"clinical_significance":[],"id":"rs1402457413","seq_region_name":"7","feature_type":"variation","strand":1,"end":140591711,"alleles":["CTTCTT","CTT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591706},{"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140591707,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591707,"source":"dbSNP","id":"rs1799034154","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140591714,"alleles":["TTCTTTCT","TTCT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591707,"clinical_significance":[],"id":"rs1020776043","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591709,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140591709,"seq_region_name":"7","id":"rs113779072","clinical_significance":[]},{"clinical_significance":[],"id":"rs1291112970","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591709,"feature_type":"variation","strand":1,"alleles":["C","CC"],"end":140591709},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591710,"feature_type":"variation","strand":1,"alleles":["-","CT","CTTCCTTCTT","CTTCTT"],"end":140591709,"clinical_significance":[],"seq_region_name":"7","id":"rs1418333647"},{"clinical_significance":[],"seq_region_name":"7","id":"rs111402942","source":"dbSNP","start":140591710,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140591710,"feature_type":"variation","strand":1},{"start":140591710,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140591712,"alleles":["TTT","T","TTTTT"],"strand":1,"feature_type":"variation","id":"rs1554475952","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs112300834","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140591711,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591711},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591712,"source":"dbSNP","strand":1,"feature_type":"variation","end":140591711,"alleles":["-","C","CCTTCTTTC","CTTTC"],"seq_region_name":"7","id":"rs1554475953","clinical_significance":[]},{"source":"dbSNP","start":140591712,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TCT","TCTTTCTCT"],"end":140591714,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1554475954"},{"seq_region_name":"7","id":"rs148130974","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591712,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TCTCTCTCT","TCTCT","TCTCTCT","TCTCTCTCTCT","TCTCTCTCTCTCT","TCTCTCTCTCTTTCCTTTCCTTTCTCTCTCTCTTTCCTTTCCTTTCTCTCTCTCT"],"end":140591720},{"id":"rs1563163937","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140591744,"alleles":["TCTCTCTCTTTCCTTTCCTTTCTCTCTCTCTTT","TCTCTCTCTTTCCTTTCCTTTCTCTCTCTCTTTCCTTTCCTTTCTCTCTCTCTTT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591712,"source":"dbSNP"},{"alleles":["C","CGC"],"end":140591713,"strand":1,"feature_type":"variation","start":140591713,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs35775974","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799036082","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591714,"feature_type":"variation","strand":1,"alleles":["T","TTT"],"end":140591714},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140591715,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591715,"source":"dbSNP","seq_region_name":"7","id":"rs1799036190","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799036321","seq_region_name":"7","source":"dbSNP","start":140591719,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140591733,"alleles":["CTTTCCTTTCCTTTC","CTTTCCTTTC"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591720,"source":"dbSNP","strand":1,"feature_type":"variation","end":140591720,"alleles":["T","G"],"id":"rs1799036429","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591720,"feature_type":"variation","strand":1,"alleles":["TTT","TT"],"end":140591722,"clinical_significance":[],"seq_region_name":"7","id":"rs1799036572"},{"seq_region_name":"7","id":"rs767002971","clinical_significance":[],"strand":1,"feature_type":"variation","end":140591720,"alleles":["-","CC"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591721,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs779001565","end":140591723,"alleles":["TTC","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140591721,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799036933","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140591723,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591723},{"alleles":["CC","C"],"end":140591724,"strand":1,"feature_type":"variation","start":140591723,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs529006253","seq_region_name":"7","clinical_significance":[]},{"id":"rs908612291","seq_region_name":"7","clinical_significance":[],"alleles":["C","G"],"end":140591724,"strand":1,"feature_type":"variation","start":140591724,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140591727,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591727,"source":"dbSNP","id":"rs1799037303","seq_region_name":"7","clinical_significance":[]},{"id":"rs902360285","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591728,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","G","T"],"end":140591728},{"clinical_significance":[],"id":"rs1436979235","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["TTT","T"],"end":140591732,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591730},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591732,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TCTCTCTCTCT","TCTCTCT","TCTCTCTCT"],"end":140591742,"seq_region_name":"7","id":"rs199843276","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140591735,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591735,"clinical_significance":[],"seq_region_name":"7","id":"rs1003594280"},{"alleles":["T","C"],"end":140591738,"strand":1,"feature_type":"variation","start":140591738,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799037967","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1394903186","feature_type":"variation","strand":1,"alleles":["TCTCTTTTCTTTCTCTTT","TCTCTTT"],"end":140591755,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591738},{"start":140591739,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["CTC","-"],"end":140591741,"strand":1,"feature_type":"variation","id":"rs1239040955","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1035101724","clinical_significance":[],"start":140591740,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140591743,"alleles":["TCTT","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1181278147","end":140591745,"alleles":["TTTT","TT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140591742,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["T","C"],"end":140591743,"strand":1,"feature_type":"variation","start":140591743,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799038548","clinical_significance":[]},{"start":140591743,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TTTCTTTCT","TTTCT"],"end":140591751,"strand":1,"feature_type":"variation","id":"rs1390187617","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591745,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140591745,"clinical_significance":[],"seq_region_name":"7","id":"rs1159375744"},{"source":"dbSNP","start":140591748,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A","C"],"end":140591748,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs544182623"},{"strand":1,"feature_type":"variation","end":140591753,"alleles":["TCTCT","TCT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591749,"source":"dbSNP","id":"rs1585708833","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140591753,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140591753,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1236461607"},{"start":140591757,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140591757,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1431119057","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs976887445","source":"dbSNP","start":140591762,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140591762,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1469338680","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591763,"feature_type":"variation","strand":1,"end":140591763,"alleles":["T","C"]},{"feature_type":"variation","strand":1,"alleles":["TCCTT","T"],"end":140591767,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591763,"clinical_significance":[],"seq_region_name":"7","id":"rs1276845999"},{"seq_region_name":"7","id":"rs1166275391","clinical_significance":[],"start":140591765,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140591767,"alleles":["CTT","-"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1585708902","clinical_significance":[],"start":140591766,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140591766,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1799039988","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591767,"source":"dbSNP","strand":1,"feature_type":"variation","end":140591774,"alleles":["TTTCTTTC","TTTC"]},{"start":140591774,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140591774,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs922737716","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591775,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140591775,"seq_region_name":"7","id":"rs1799040205","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591778,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140591778,"seq_region_name":"7","id":"rs932917223","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1240446777","source":"dbSNP","start":140591779,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140591779,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1369592814","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591779,"feature_type":"variation","strand":1,"end":140591790,"alleles":["CTTTCTTTCTTT","CTTTCTTT"]},{"feature_type":"variation","strand":1,"alleles":["CTTTCTTTCTTTTCTTTTCTTTCTTTCTTTT","CTTTCTTTCTTTT"],"end":140591809,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591779,"clinical_significance":[],"seq_region_name":"7","id":"rs1288631779"},{"source":"dbSNP","start":140591780,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TTTCTTTCTTTTCTTTTCTTTCTTT","TTTCTTTCTTT"],"end":140591804,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1414723030"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1335248289","source":"dbSNP","start":140591782,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140591782,"alleles":["T","C"],"feature_type":"variation","strand":1},{"start":140591784,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140591800,"alleles":["TTTCTTTTCTTTTCTTT","TTTCTTTTCTTT","TTTCTTTTCTTTTCTTTTCTTT"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs959518930","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591785,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140591785,"clinical_significance":[],"seq_region_name":"7","id":"rs1049944165"},{"alleles":["TTCTT","TT"],"end":140591789,"strand":1,"feature_type":"variation","start":140591785,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1342695116","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591788,"source":"dbSNP","strand":1,"feature_type":"variation","end":140591788,"alleles":["T","C"],"seq_region_name":"7","id":"rs1433951845","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1016959113","source":"dbSNP","start":140591788,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140591791,"alleles":["TTTT","-"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140591789,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140591789,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799041668","seq_region_name":"7"},{"id":"rs1365942844","seq_region_name":"7","clinical_significance":[],"end":140591804,"alleles":["TTTCTTTTCTTTCTTT","TTTCTTT"],"strand":1,"feature_type":"variation","start":140591789,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591790,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TTCTT","TT"],"end":140591794,"seq_region_name":"7","id":"rs1230726071","clinical_significance":[]},{"end":140591791,"alleles":["-","TC"],"strand":1,"feature_type":"variation","start":140591792,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799042035","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140591796,"alleles":["TTTT","TT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591793,"source":"dbSNP","seq_region_name":"7","id":"rs1421789094","clinical_significance":[]},{"seq_region_name":"7","id":"rs201238063","clinical_significance":[],"start":140591794,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TTTCTTTCTTTCTTT","TTTCTTT","TTTCTTTCTTT"],"end":140591808,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140591795,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140591799,"alleles":["TTCTT","TT"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799042552"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1413195833","source":"dbSNP","start":140591796,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140591796,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591796,"feature_type":"variation","strand":1,"end":140591798,"alleles":["TCT","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799042832"},{"clinical_significance":[],"id":"rs1427711995","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140591797,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591797},{"feature_type":"variation","strand":1,"end":140591800,"alleles":["TTT","TT","TTTT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591798,"clinical_significance":[],"id":"rs1799043218","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1338963160","alleles":["TTCTT","TT"],"end":140591803,"feature_type":"variation","strand":1,"source":"dbSNP","start":140591799,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140591800,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140591806,"alleles":["TCTTTCT","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1201305253"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799043639","end":140591804,"alleles":["TTT","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140591802,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140591803,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140591803,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1799043796","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591805,"source":"dbSNP","strand":1,"feature_type":"variation","end":140591805,"alleles":["C","T"],"seq_region_name":"7","id":"rs1585709116","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799044055","source":"dbSNP","start":140591806,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TTTTT","T"],"end":140591810,"feature_type":"variation","strand":1},{"start":140591808,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140591808,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs569096458","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591811,"source":"dbSNP","strand":1,"feature_type":"variation","end":140591811,"alleles":["C","G","T"],"seq_region_name":"7","id":"rs1799044325","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799044589","clinical_significance":[],"start":140591812,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140591812,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"alleles":["TTCTCTTTCTTTC","TTC"],"end":140591825,"feature_type":"variation","strand":1,"source":"dbSNP","start":140591813,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1189995731"},{"id":"rs1477876059","seq_region_name":"7","clinical_significance":[],"start":140591814,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140591818,"alleles":["TCTCT","TCT"],"strand":1,"feature_type":"variation"},{"id":"rs1440490003","seq_region_name":"7","clinical_significance":[],"alleles":["TTT","T"],"end":140591820,"strand":1,"feature_type":"variation","start":140591818,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140591822,"alleles":["TCT","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591820,"source":"dbSNP","id":"rs1202893163","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs963267372","seq_region_name":"7","end":140591821,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140591821,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1799045414","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140591822,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591822,"source":"dbSNP"},{"source":"dbSNP","start":140591824,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140591839,"alleles":["TCCCTCCCTCCCTCCC","TCCCTCCCTCCC"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs972974320","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799045675","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591825,"source":"dbSNP","strand":1,"feature_type":"variation","end":140591825,"alleles":["C","A"]},{"seq_region_name":"7","id":"rs1585709182","clinical_significance":[],"start":140591828,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140591828,"alleles":["T","C","G"],"strand":1,"feature_type":"variation"},{"end":140591829,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140591829,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799045905","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591832,"feature_type":"variation","strand":1,"end":140591832,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1283242979"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591833,"feature_type":"variation","strand":1,"alleles":["CCCTCCCCTTCCTTCTTTCCTTCCTTCCCTTCCCTTTCCTTCCTTCCTTCTTTCTTTCTTTCTTTTTCTTCCTCTCTCTTTCTCCTCCCTTCCCTTCCCTCCCCTCCCCTCCCCCCTCCCTACTCCCCTCCCCTCCCCCTCCCCTCTCCCTCCTCTCCCCTCCCCTTCC","CCCTCCCCTTCC"],"end":140592001,"clinical_significance":[],"seq_region_name":"7","id":"rs1799046149"},{"source":"dbSNP","start":140591833,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["CCCTCCCCTTCCTTCTTTCCTTCCTTCCCTTCCCTTTCCTTCCTTCCTTCTTTCTTTCTTTCTTTTTCTTCCTCTCTCTTTCTCCTCCCTTCCCTTCCCTCCCCTCCCCTCCCCCCTCCCTACTCCCCTCCCCTCCCCCTCCCCTCTCCCTCCTCTCCCCTCCCCTTCCCCTCTCCCTCCTCTCCCCTCCCCTCCCCTTC","CCCTCCCCTTC"],"end":140592032,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799046261"},{"end":140591836,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140591836,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1215340319","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799046531","seq_region_name":"7","source":"dbSNP","start":140591838,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140591865,"alleles":["CCCTTCCTTCTTTCCTTCCTTCCCTTCC","CCCTTCC"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs2130661159","clinical_significance":[],"end":140591838,"alleles":["-","TT"],"strand":1,"feature_type":"variation","start":140591839,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140591839,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140591839,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1312273176"},{"clinical_significance":[],"id":"rs1799046773","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591840,"feature_type":"variation","strand":1,"end":140591840,"alleles":["C","T"]},{"clinical_significance":[],"id":"rs1585709238","seq_region_name":"7","alleles":["T","C"],"end":140591841,"feature_type":"variation","strand":1,"source":"dbSNP","start":140591841,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1303250012","source":"dbSNP","start":140591845,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140591851,"alleles":["TTCTTTC","TTC"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1217430181","seq_region_name":"7","source":"dbSNP","start":140591847,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140591879,"alleles":["CTTTCCTTCCTTCCCTTCCCTTTCCTTCCTTCC","CTTTCCTTCCTTCC"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140591848,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591848,"source":"dbSNP","seq_region_name":"7","id":"rs2130661195","clinical_significance":[]},{"end":140591860,"alleles":["TTCCTTCCTTCC","TTCCTTCC"],"strand":1,"feature_type":"variation","start":140591849,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799047277","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1450749602","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591851,"feature_type":"variation","strand":1,"end":140591865,"alleles":["CCTTCCTTCCCTTCC","CCTTCCTTCCCTTCCTTCCCTTCC"]},{"seq_region_name":"7","id":"rs1799047541","clinical_significance":[],"start":140591854,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140591854,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591855,"feature_type":"variation","strand":1,"alleles":["CCTTCCCTTCCCTT","CCTTCCCTT","CCTTCCCTTCCCTTCCCTT"],"end":140591868,"clinical_significance":[],"seq_region_name":"7","id":"rs1186088456"},{"seq_region_name":"7","id":"rs1799047905","clinical_significance":[],"alleles":["T","G"],"end":140591858,"strand":1,"feature_type":"variation","start":140591858,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["CCTTCCCTTTCCTTCC","CCTTCC"],"end":140591875,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591860,"source":"dbSNP","id":"rs1799048099","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799048331","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["TT","TTT"],"end":140591863,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591862},{"start":140591863,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140591863,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1478143330","clinical_significance":[]},{"seq_region_name":"7","id":"rs1297654369","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591865,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CCTTTCCTT","CCTT"],"end":140591873},{"end":140591866,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140591866,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1174033015","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1174523268","feature_type":"variation","strand":1,"end":140591869,"alleles":["TTT","TT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591867},{"clinical_significance":[],"id":"rs918723214","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591868,"feature_type":"variation","strand":1,"end":140591882,"alleles":["TTCCTTCCTTCCTTC","TTCCTTCCTTC","TTCCTTCCTTCCTTCCTTC"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591869,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140591869,"seq_region_name":"7","id":"rs1413130216","clinical_significance":[]},{"source":"dbSNP","start":140591872,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140591873,"alleles":["TT","TTT"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1336587810"},{"alleles":["TCCT","T"],"end":140591876,"feature_type":"variation","strand":1,"source":"dbSNP","start":140591873,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130661295"},{"clinical_significance":[],"id":"rs530299874","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591874,"feature_type":"variation","strand":1,"end":140591874,"alleles":["C","G","T"]},{"id":"rs1799049665","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591875,"source":"dbSNP","strand":1,"feature_type":"variation","end":140591875,"alleles":["C","T"]},{"clinical_significance":[],"id":"rs1192504761","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591879,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140591879},{"seq_region_name":"7","id":"rs1799049954","clinical_significance":[],"end":140591884,"alleles":["CTTCTT","CTT"],"strand":1,"feature_type":"variation","start":140591879,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1799050083","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591880,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140591880},{"strand":1,"feature_type":"variation","end":140591897,"alleles":["TTCTTTCTTTCTTTCTTT","TTCTTTCTTT","TTCTTTCTTTCTTT","TTCTTTCTTTCTTTCTTTCTTT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591880,"source":"dbSNP","seq_region_name":"7","id":"rs533126680","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591883,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140591883,"seq_region_name":"7","id":"rs112892518","clinical_significance":[]},{"alleles":["TTT","T"],"end":140591885,"feature_type":"variation","strand":1,"source":"dbSNP","start":140591883,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799050858"},{"strand":1,"feature_type":"variation","alleles":["TCT","T"],"end":140591887,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591885,"source":"dbSNP","seq_region_name":"7","id":"rs1799051044","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799051140","clinical_significance":[],"end":140591889,"alleles":["TTT","T"],"strand":1,"feature_type":"variation","start":140591887,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["TTCTT","TT"],"end":140591892,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591888,"clinical_significance":[],"seq_region_name":"7","id":"rs1295482479"},{"alleles":["TCT","T"],"end":140591891,"feature_type":"variation","strand":1,"source":"dbSNP","start":140591889,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1311584371","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1293624086","source":"dbSNP","start":140591891,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TTT","T","TTTTT"],"end":140591893,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["TTTCTTTT","TTT"],"end":140591898,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591891,"source":"dbSNP","id":"rs1220308973","seq_region_name":"7","clinical_significance":[]},{"end":140591892,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140591892,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs373454730"},{"seq_region_name":"7","id":"rs1234151804","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["TTCTT","TT"],"end":140591896,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591892,"source":"dbSNP"},{"seq_region_name":"7","id":"rs367947897","clinical_significance":[],"end":140591895,"alleles":["TCT","TCTCT","TCTGTCT"],"strand":1,"feature_type":"variation","start":140591893,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591895,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140591895,"clinical_significance":[],"seq_region_name":"7","id":"rs1799052646"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591896,"source":"dbSNP","strand":1,"feature_type":"variation","end":140591895,"alleles":["-","C","GTC"],"seq_region_name":"7","id":"rs1563164146","clinical_significance":[]},{"id":"rs1276845007","seq_region_name":"7","clinical_significance":[],"start":140591896,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140591896,"strand":1,"feature_type":"variation"},{"end":140591903,"alleles":["TTCTTC","TTC"],"strand":1,"feature_type":"variation","start":140591898,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1799053278","seq_region_name":"7","clinical_significance":[]},{"start":140591900,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140591900,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1342552684","clinical_significance":[]},{"seq_region_name":"7","id":"rs1222705941","clinical_significance":[],"end":140591911,"alleles":["CTCTCTCT","CTCT","CTCTCT"],"strand":1,"feature_type":"variation","start":140591904,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140591907,"alleles":["T","C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591907,"clinical_significance":[],"seq_region_name":"7","id":"rs1423387978"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799054214","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591909,"feature_type":"variation","strand":1,"alleles":["TCTTTCT","TCT"],"end":140591915},{"clinical_significance":[],"seq_region_name":"7","id":"rs1169469394","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591915,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140591915},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591916,"feature_type":"variation","strand":1,"end":140591916,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1424074849"},{"start":140591918,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TCCCTTCCCTTCCCT","TCCCTTCCCT"],"end":140591932,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1257635251","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799055075","clinical_significance":[],"end":140591919,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140591919,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs865948484","clinical_significance":[],"end":140591921,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140591921,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140591922,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140591922,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799055504"},{"id":"rs1799055697","seq_region_name":"7","clinical_significance":[],"end":140591923,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140591923,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1799055872","clinical_significance":[],"end":140591924,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140591924,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140591942,"alleles":["CCCTTCCCTCCCCTCCCCT","CCCT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591924,"clinical_significance":[],"id":"rs1466181038","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799056184","feature_type":"variation","strand":1,"end":140591926,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591926},{"id":"rs1585709572","seq_region_name":"7","clinical_significance":[],"start":140591927,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140591927,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140591928,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A","C"],"end":140591928,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585709581"},{"clinical_significance":[],"id":"rs1238643298","seq_region_name":"7","source":"dbSNP","start":140591929,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["CCCTCCCCTCCCCTCCCC","CCCTCCCCTCCCC","CCCTCCCCTCCCCTCCCCTCCCC"],"end":140591946,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140591929,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140592030,"alleles":["CCCTCCCCTCCCCTCCCCCCTCCCTACTCCCCTCCCCTCCCCCTCCCCTCTCCCTCCTCTCCCCTCCCCTTCCCCTCTCCCTCCTCTCCCCTCCCCTCCCCT","CCCTCCCCT"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799056739"},{"feature_type":"variation","strand":1,"end":140591930,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591930,"clinical_significance":[],"seq_region_name":"7","id":"rs1799056873"},{"end":140591971,"alleles":["CTCCCCTCCCCTCCCCCCTCCCTACTCCCCTCCCCTCCCCC","CTCCCCTCCCCTCCCCC","CTCCCCTCCCCTCCCCCCTCCCTACTCCCCTCCCCTCCCCCCTCCCTACTCCCCTCCCCTCCCCC"],"strand":1,"feature_type":"variation","start":140591931,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1200476402","clinical_significance":[]},{"source":"dbSNP","start":140591932,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140591932,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1585709611","seq_region_name":"7"},{"id":"rs1799057300","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591933,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140591933},{"clinical_significance":[],"id":"rs1799057413","seq_region_name":"7","source":"dbSNP","start":140591936,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["CTCCCCTCCCCCCTCCCTACTCCCCTCCCC","CTCCCCTCCCC"],"end":140591965,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1315790805","clinical_significance":[],"alleles":["T","C"],"end":140591937,"strand":1,"feature_type":"variation","start":140591937,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140591938,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140591938,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1799057658","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140591938,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["CCCC","CCCCC"],"end":140591941,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799057775"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799057904","source":"dbSNP","start":140591938,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140591948,"alleles":["CCCCTCCCCCC","CCC"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1257231534","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["CCCCTCCCCCCTCCC","CCCCTCCC"],"end":140591952,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591938,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130661654","feature_type":"variation","strand":1,"alleles":["-","T"],"end":140591938,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591939},{"alleles":["C","T"],"end":140591939,"feature_type":"variation","strand":1,"source":"dbSNP","start":140591939,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1245764121"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591941,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140591941,"seq_region_name":"7","id":"rs1585709643","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1323789073","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591942,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140591942},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799058530","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591942,"feature_type":"variation","strand":1,"end":140591942,"alleles":["T","TT"]},{"strand":1,"feature_type":"variation","end":140591948,"alleles":["CCCCCC","CCCCC","CCCCCCCCCCC"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591943,"source":"dbSNP","seq_region_name":"7","id":"rs1260427381","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140591944,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591944,"clinical_significance":[],"seq_region_name":"7","id":"rs1395455203"},{"end":140591945,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140591945,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799058807","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591946,"source":"dbSNP","strand":1,"feature_type":"variation","end":140591946,"alleles":["C","A"],"seq_region_name":"7","id":"rs1377759131","clinical_significance":[]},{"id":"rs1585709710","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591947,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","G","T"],"end":140591947},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591948,"feature_type":"variation","strand":1,"alleles":["C","A","G","T"],"end":140591948,"clinical_significance":[],"seq_region_name":"7","id":"rs1451677024"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1399990045","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591949,"feature_type":"variation","strand":1,"end":140591949,"alleles":["T","C"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591949,"source":"dbSNP","strand":1,"feature_type":"variation","end":140591949,"alleles":["T","-"],"seq_region_name":"7","id":"rs1445263390","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799059822","clinical_significance":[],"end":140591952,"alleles":["CCC","CC"],"strand":1,"feature_type":"variation","start":140591950,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140591952,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","G"],"end":140591952,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585709754","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799060095","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["CTACT","CT"],"end":140591956,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591952,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799060219","clinical_significance":[],"alleles":["CTACTC","C"],"end":140591957,"strand":1,"feature_type":"variation","start":140591952,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591953,"feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140591953,"clinical_significance":[],"id":"rs1585709767","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1294539951","end":140591954,"alleles":["TA","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140591953,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140591956,"alleles":["TACT","-"],"strand":1,"feature_type":"variation","start":140591953,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799060604","clinical_significance":[]},{"seq_region_name":"7","id":"rs1238215689","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591954,"source":"dbSNP","strand":1,"feature_type":"variation","end":140591954,"alleles":["A","C","G","T"]},{"strand":1,"feature_type":"variation","end":140591955,"alleles":["AC","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591954,"source":"dbSNP","id":"rs1799060934","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1200474359","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["ACTCC","-"],"end":140591958,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591954},{"clinical_significance":[],"seq_region_name":"7","id":"rs1375590760","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591955,"feature_type":"variation","strand":1,"end":140591955,"alleles":["C","A","T"]},{"feature_type":"variation","strand":1,"end":140591970,"alleles":["CTCCCCTCCCCTCCCC","CTCCCCTCCCC"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591955,"clinical_significance":[],"seq_region_name":"7","id":"rs1380409713"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591956,"source":"dbSNP","strand":1,"feature_type":"variation","end":140591956,"alleles":["T","C","G"],"seq_region_name":"7","id":"rs1180400020","clinical_significance":[]},{"alleles":["CCCC","C"],"end":140591960,"strand":1,"feature_type":"variation","start":140591957,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799061636","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799061749","clinical_significance":[],"start":140591957,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140591965,"alleles":["CCCCTCCCC","CCCCTCCCCCTCCCC"],"strand":1,"feature_type":"variation"},{"start":140591957,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140591978,"alleles":["CCCCTCCCCTCCCCCTCCCCTC","CCCCTCCCCTC","CCCCTCCCCTCCCCCTCCCCTCCCCCTCCCCTC"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1456425120","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140591958,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591958,"clinical_significance":[],"seq_region_name":"7","id":"rs1585709863"},{"end":140591959,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140591959,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1210277803"},{"seq_region_name":"7","id":"rs1563164212","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["CCTCC","CC"],"end":140591963,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591959,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["CCTCCC","CCTCCCTCCTCCC"],"end":140591964,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591959,"source":"dbSNP","seq_region_name":"7","id":"rs1799062430","clinical_significance":[]},{"seq_region_name":"7","id":"rs1176137595","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591960,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140591960},{"feature_type":"variation","strand":1,"end":140591964,"alleles":["CTCCC","CTCCCTACTCCC"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591960,"clinical_significance":[],"seq_region_name":"7","id":"rs1479636234"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591961,"source":"dbSNP","strand":1,"feature_type":"variation","end":140591961,"alleles":["T","A","C"],"seq_region_name":"7","id":"rs1263841433","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140591961,"alleles":["T","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591961,"clinical_significance":[],"seq_region_name":"7","id":"rs1799062959"},{"start":140591962,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140591962,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs867884828","clinical_significance":[]},{"seq_region_name":"7","id":"rs1441070394","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["CCCC","CCCCC"],"end":140591965,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591962,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140591963,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591963,"source":"dbSNP","id":"rs1585709932","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1311611675","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140591964,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591964},{"seq_region_name":"7","id":"rs1799063632","clinical_significance":[],"alleles":["C","CTC"],"end":140591964,"strand":1,"feature_type":"variation","start":140591964,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1799063747","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591964,"source":"dbSNP","strand":1,"feature_type":"variation","end":140591965,"alleles":["CC","CCCTCCCCTCTCCCTCC"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591965,"feature_type":"variation","strand":1,"alleles":["-","TA"],"end":140591964,"clinical_significance":[],"seq_region_name":"7","id":"rs1354461292"},{"seq_region_name":"7","id":"rs1585709951","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140591965,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591965,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["C","CCTCCCCTCTCCCTCCTC"],"end":140591965,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591965,"clinical_significance":[],"seq_region_name":"7","id":"rs1799064078"},{"id":"rs868548217","seq_region_name":"7","clinical_significance":[],"end":140591966,"alleles":["T","C","G"],"strand":1,"feature_type":"variation","start":140591966,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799064374","source":"dbSNP","start":140591966,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TCCCCCTCCCCT","-"],"end":140591977,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs865795187","source":"dbSNP","start":140591967,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140591967,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1376888440","clinical_significance":[],"start":140591967,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["CCCCC","CCCC","CCCCCC"],"end":140591971,"strand":1,"feature_type":"variation"},{"end":140591967,"alleles":["-","T","TCCCTCCTCT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140591968,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1459282704"},{"clinical_significance":[],"id":"rs1389043956","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591968,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140591968},{"seq_region_name":"7","id":"rs1799065047","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591968,"source":"dbSNP","strand":1,"feature_type":"variation","end":140591970,"alleles":["CCC","CCCTCCC"]},{"end":140591975,"alleles":["CCCCTCCC","CCCCTCCCTCCTCTCCCCTCCC"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140591968,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1554476083","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799065282","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591968,"source":"dbSNP","strand":1,"feature_type":"variation","end":140591998,"alleles":["CCCCTCCCCTCTCCCTCCTCTCCCCTCCCCT","CCCCTCCCCT"]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140591970,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591970,"source":"dbSNP","seq_region_name":"7","id":"rs1585710008","clinical_significance":[]},{"source":"dbSNP","start":140591971,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140591970,"alleles":["-","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1319139472"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1291388844","source":"dbSNP","start":140591971,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140591971,"alleles":["C","T"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140591972,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591972,"source":"dbSNP","seq_region_name":"7","id":"rs1360578516","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591972,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","-"],"end":140591972,"id":"rs1799065912","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591972,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TCCCCTCTCCCTCCTCTCCCCTCCCCTTCCCCTCTCCCTCCTCTCCCCTCCCCT","TCCCCTCTCCCTCCTCTCCCCTCCCCT"],"end":140592025,"id":"rs1384274390","seq_region_name":"7","clinical_significance":[]},{"id":"rs1585710061","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591973,"source":"dbSNP","strand":1,"feature_type":"variation","end":140591973,"alleles":["C","A","T"]},{"source":"dbSNP","start":140591974,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140591974,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1159992991"},{"end":140591975,"alleles":["C","CTC"],"strand":1,"feature_type":"variation","start":140591975,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1423957051","clinical_significance":[]},{"start":140591975,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140591991,"alleles":["CCTCTCCCTCCTCTCCC","CCTCTCCC","CCTCTCCCTCCTCTCCCTCCTCTCCC"],"strand":1,"feature_type":"variation","id":"rs1799066519","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585710110","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591976,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140591976},{"start":140591976,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["CTCTCCCTCCTCTC","CTC"],"end":140591989,"strand":1,"feature_type":"variation","id":"rs1799066819","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","C"],"end":140591977,"feature_type":"variation","strand":1,"source":"dbSNP","start":140591977,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585710125"},{"source":"dbSNP","start":140591977,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","-"],"end":140591977,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799067052"},{"seq_region_name":"7","id":"rs1437740398","clinical_significance":[],"strand":1,"feature_type":"variation","end":140591978,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591978,"source":"dbSNP"},{"start":140591979,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140591979,"strand":1,"feature_type":"variation","id":"rs1379534679","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1763920875","source":"dbSNP","start":140591979,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","-"],"end":140591979,"feature_type":"variation","strand":1},{"id":"rs1799067300","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591980,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140591980},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140591981,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591981,"clinical_significance":[],"seq_region_name":"7","id":"rs1585710153"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1199504953","alleles":["C","T"],"end":140591982,"feature_type":"variation","strand":1,"source":"dbSNP","start":140591982,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799067676","end":140591984,"alleles":["CTC","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140591982,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591983,"feature_type":"variation","strand":1,"alleles":["-","CTCCCCTCCCCT"],"end":140591982,"clinical_significance":[],"seq_region_name":"7","id":"rs1387450592"},{"end":140591983,"alleles":["T","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140591983,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585710178"},{"id":"rs1799068046","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591983,"source":"dbSNP","strand":1,"feature_type":"variation","end":140591986,"alleles":["TCCT","-"]},{"clinical_significance":[],"id":"rs1177909850","seq_region_name":"7","end":140591986,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140591986,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["CTCCCCTCCCCT","CTCCCCTCCCCTCCCCTTCCCCTCCCCTCCCCT","CTCCCCTCCCCTCCCCTTCCCCTCCCCTCCCCTCCCCT"],"end":140591998,"feature_type":"variation","strand":1,"source":"dbSNP","start":140591987,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799068321"},{"start":140591990,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140591990,"strand":1,"feature_type":"variation","id":"rs1799068454","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585710204","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591992,"source":"dbSNP","strand":1,"feature_type":"variation","end":140591992,"alleles":["C","A"]},{"seq_region_name":"7","id":"rs1585710242","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591993,"source":"dbSNP","strand":1,"feature_type":"variation","end":140591993,"alleles":["T","C"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591994,"source":"dbSNP","strand":1,"feature_type":"variation","end":140591994,"alleles":["C","T"],"id":"rs1799068813","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1265043899","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140591995,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591995,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1585710272","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140591996,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140591996,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591997,"feature_type":"variation","strand":1,"end":140591997,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585710286"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1209436456","source":"dbSNP","start":140591998,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C","G"],"end":140591998,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1799069462","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140591998,"feature_type":"variation","strand":1,"alleles":["TT","T"],"end":140591999},{"seq_region_name":"7","id":"rs1325732538","clinical_significance":[],"start":140591999,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140591999,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1288241544","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592001,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140592001},{"source":"dbSNP","start":140592004,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","-"],"end":140592004,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1214631935","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140592004,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592004,"source":"dbSNP","seq_region_name":"7","id":"rs1585710354","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799070053","feature_type":"variation","strand":1,"end":140592005,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592005},{"end":140592009,"alleles":["CTCCC","-"],"strand":1,"feature_type":"variation","start":140592005,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799070185","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1353082889","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140592006,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592006},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799070423","source":"dbSNP","start":140592007,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140592007,"alleles":["C","G"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140592010,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140592010,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585710393"},{"seq_region_name":"7","id":"rs1585710405","clinical_significance":[],"alleles":["C","A"],"end":140592011,"strand":1,"feature_type":"variation","start":140592011,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1799070732","clinical_significance":[],"alleles":["CTCTC","CTCTCTC"],"end":140592016,"strand":1,"feature_type":"variation","start":140592012,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140592013,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592013,"source":"dbSNP","seq_region_name":"7","id":"rs1275902803","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592014,"feature_type":"variation","strand":1,"end":140592030,"alleles":["CTCCCCTCCCCTCCCCT","CTCCCCT","CTCCCCTCCCCT","CTCCCCTCCCCTCCCCTCCCCT","CTCCCCTCCCCTCCCCTCCCCTCCCCT"],"clinical_significance":[],"seq_region_name":"7","id":"rs1236099741"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1329678801","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592015,"feature_type":"variation","strand":1,"end":140592015,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1024218303","clinical_significance":[],"start":140592020,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140592020,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1301072140","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592021,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140592021},{"seq_region_name":"7","id":"rs1585710466","clinical_significance":[],"start":140592022,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140592022,"alleles":["C","A","T"],"strand":1,"feature_type":"variation"},{"alleles":["C","G","T"],"end":140592024,"strand":1,"feature_type":"variation","start":140592024,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1223182132","clinical_significance":[]},{"id":"rs1299653470","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140592025,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592025,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140592029,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592029,"clinical_significance":[],"id":"rs1799071958","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1417254017","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140592030,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592030,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799072492","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592032,"feature_type":"variation","strand":1,"end":140592032,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1288730011","clinical_significance":[],"start":140592035,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TTCTTCTTCTT","TTCTTCTT"],"end":140592045,"strand":1,"feature_type":"variation"},{"end":140592037,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140592037,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1331033350","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","G"],"end":140592038,"strand":1,"feature_type":"variation","start":140592038,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1799072896","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1467561830","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140592039,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592039,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140592040,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592040,"clinical_significance":[],"seq_region_name":"7","id":"rs1410096586"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1198500792","feature_type":"variation","strand":1,"end":140592041,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592041},{"seq_region_name":"7","id":"rs1226426088","clinical_significance":[],"start":140592041,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140592046,"alleles":["TTCTTT","TT"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140592042,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140592042,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585710569"},{"alleles":["C","G","T"],"end":140592043,"strand":1,"feature_type":"variation","start":140592043,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1265527887","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799073988","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592044,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140592044},{"seq_region_name":"7","id":"rs541459225","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592044,"source":"dbSNP","strand":1,"feature_type":"variation","end":140592057,"alleles":["TTTTTTTTTTTTTT","TTTTTTTTTTT","TTTTTTTTTTTT","TTTTTTTTTTTTT","TTTTTTTTTTTTTTT"]},{"start":140592045,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140592045,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1260083984","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592046,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140592046,"seq_region_name":"7","id":"rs1356376000","clinical_significance":[]},{"id":"rs1279470248","seq_region_name":"7","clinical_significance":[],"start":140592047,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140592047,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"start":140592051,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140592051,"strand":1,"feature_type":"variation","id":"rs1202678316","seq_region_name":"7","clinical_significance":[]},{"end":140592057,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140592057,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1343563960"},{"alleles":["G","C","T"],"end":140592058,"strand":1,"feature_type":"variation","start":140592058,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs969699008","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799075189","feature_type":"variation","strand":1,"alleles":["G","-"],"end":140592058,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592058},{"seq_region_name":"7","id":"rs1264718379","clinical_significance":[],"start":140592059,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140592059,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs182220283","seq_region_name":"7","feature_type":"variation","strand":1,"end":140592060,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592060},{"source":"dbSNP","start":140592061,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140592061,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799075595"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585710690","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592063,"feature_type":"variation","strand":1,"end":140592063,"alleles":["A","C","G"]},{"start":140592064,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140592064,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799075904","clinical_significance":[]},{"seq_region_name":"7","id":"rs1182540894","clinical_significance":[],"alleles":["C","A","T"],"end":140592068,"strand":1,"feature_type":"variation","start":140592068,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140592069,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592069,"source":"dbSNP","id":"rs1325322556","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","C","T"],"end":140592076,"strand":1,"feature_type":"variation","start":140592076,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585710729","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1334301915","feature_type":"variation","strand":1,"end":140592077,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592077},{"seq_region_name":"7","id":"rs1799076636","clinical_significance":[],"end":140592078,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140592078,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140592079,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140592079,"alleles":["C","A"],"strand":1,"feature_type":"variation","id":"rs1799076780","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799076915","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592079,"feature_type":"variation","strand":1,"alleles":["CCC","CC"],"end":140592081},{"end":140592099,"alleles":["CCCAGGCTCTTGTCACCCAGG","CCCAGGCTCTTGTCACCCAGGCTCTTGTCACCCAGG"],"strand":1,"feature_type":"variation","start":140592079,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799077020","clinical_significance":[]},{"clinical_significance":[],"id":"rs1585710750","seq_region_name":"7","end":140592082,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140592082,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["G","C"],"end":140592083,"strand":1,"feature_type":"variation","start":140592083,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799077270","clinical_significance":[]},{"clinical_significance":[],"id":"rs1332036797","seq_region_name":"7","source":"dbSNP","start":140592084,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140592084,"alleles":["G","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1397704665","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140592085,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592085,"source":"dbSNP"},{"alleles":["T","C"],"end":140592086,"strand":1,"feature_type":"variation","start":140592086,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799077700","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799077805","seq_region_name":"7","end":140592087,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140592087,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140592093,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","start":140592093,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1400067265","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585710795","end":140592094,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140592094,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140592097,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140592097,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585710816"},{"seq_region_name":"7","id":"rs974694885","clinical_significance":[],"start":140592099,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140592099,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799078373","end":140592102,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140592102,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1585710842","clinical_significance":[],"end":140592103,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140592103,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140592104,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140592104,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1465893807","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1473784338","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592108,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140592108},{"feature_type":"variation","strand":1,"end":140592109,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592109,"clinical_significance":[],"seq_region_name":"7","id":"rs1157495861"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592110,"feature_type":"variation","strand":1,"end":140592110,"alleles":["G","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1363761261"},{"seq_region_name":"7","id":"rs1799079091","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592113,"source":"dbSNP","strand":1,"feature_type":"variation","end":140592113,"alleles":["C","T"]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140592114,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592114,"source":"dbSNP","seq_region_name":"7","id":"rs1458902714","clinical_significance":[]},{"source":"dbSNP","start":140592114,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["GCTGCAGC","GC"],"end":140592121,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799079322"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585710909","alleles":["A","C"],"end":140592119,"feature_type":"variation","strand":1,"source":"dbSNP","start":140592119,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140592123,"alleles":["T","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140592123,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs111311340","seq_region_name":"7"},{"start":140592123,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140592123,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799079552","clinical_significance":[]},{"end":140592125,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140592125,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1563164385"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592126,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140592126,"seq_region_name":"7","id":"rs1799079935","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs934165739","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592127,"feature_type":"variation","strand":1,"end":140592127,"alleles":["C","G","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs187188216","end":140592130,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140592130,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140592132,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592132,"source":"dbSNP","seq_region_name":"7","id":"rs1585710960","clinical_significance":[]},{"alleles":["G","A"],"end":140592134,"strand":1,"feature_type":"variation","start":140592134,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799080450","clinical_significance":[]},{"id":"rs1799080568","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592135,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140592135},{"alleles":["T","G"],"end":140592136,"strand":1,"feature_type":"variation","start":140592136,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs919939733","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","C"],"end":140592139,"strand":1,"feature_type":"variation","start":140592139,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585710987","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585711002","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592140,"feature_type":"variation","strand":1,"end":140592140,"alleles":["A","C","G"]},{"seq_region_name":"7","id":"rs1320397191","clinical_significance":[],"alleles":["G","C"],"end":140592141,"strand":1,"feature_type":"variation","start":140592141,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140592142,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140592142,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1404563901","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592144,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140592144,"seq_region_name":"7","id":"rs1799081291","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140592147,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592147,"clinical_significance":[],"seq_region_name":"7","id":"rs1256606736"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140592153,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592153,"clinical_significance":[],"seq_region_name":"7","id":"rs911621721"},{"alleles":["C","T"],"end":140592154,"strand":1,"feature_type":"variation","start":140592154,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1799081656","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799081768","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592156,"feature_type":"variation","strand":1,"end":140592156,"alleles":["C","G"]},{"clinical_significance":[],"id":"rs1585711044","seq_region_name":"7","alleles":["A","C"],"end":140592157,"feature_type":"variation","strand":1,"source":"dbSNP","start":140592157,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1308870124","seq_region_name":"7","clinical_significance":[],"end":140592164,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140592164,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs191010593","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140592165,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592165,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592166,"feature_type":"variation","strand":1,"end":140592166,"alleles":["A","T"],"clinical_significance":[],"id":"rs1407786239","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1306147657","alleles":["A","G"],"end":140592174,"feature_type":"variation","strand":1,"source":"dbSNP","start":140592174,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1246268392","alleles":["A","G"],"end":140592176,"feature_type":"variation","strand":1,"source":"dbSNP","start":140592176,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140592181,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140592181,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585711109"},{"seq_region_name":"7","id":"rs2130663023","clinical_significance":[],"start":140592183,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140592183,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1338206183","clinical_significance":[],"start":140592184,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140592184,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592185,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140592185,"seq_region_name":"7","id":"rs1340956970","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799083061","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592186,"feature_type":"variation","strand":1,"alleles":["C","A","G","T"],"end":140592186},{"source":"dbSNP","start":140592187,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140592187,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1402169607"},{"alleles":["C","T"],"end":140592190,"strand":1,"feature_type":"variation","start":140592190,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1799083356","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["CCACCAC","CCAC"],"end":140592196,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592190,"source":"dbSNP","seq_region_name":"7","id":"rs1329115828","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140592194,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592194,"clinical_significance":[],"seq_region_name":"7","id":"rs1799083584"},{"source":"dbSNP","start":140592194,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140592197,"alleles":["CACA","CA"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1246981159","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585711175","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592195,"feature_type":"variation","strand":1,"end":140592195,"alleles":["A","C"]},{"end":140592196,"alleles":["C","-"],"strand":1,"feature_type":"variation","start":140592196,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799083840","clinical_significance":[]},{"alleles":["A","C","G"],"end":140592197,"feature_type":"variation","strand":1,"source":"dbSNP","start":140592197,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs182728105","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799084159","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592198,"source":"dbSNP","strand":1,"feature_type":"variation","end":140592198,"alleles":["T","A"]},{"clinical_significance":[],"id":"rs1358117826","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592199,"feature_type":"variation","strand":1,"end":140592198,"alleles":["-","GC"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592202,"source":"dbSNP","strand":1,"feature_type":"variation","end":140592202,"alleles":["G","A"],"id":"rs1414718821","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799084410","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592207,"feature_type":"variation","strand":1,"end":140592211,"alleles":["TTTTT","TTTTTT"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs76348185","end":140592210,"alleles":["T","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140592210,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592211,"source":"dbSNP","strand":1,"feature_type":"variation","end":140592211,"alleles":["T","C"],"id":"rs1799084696","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","TGT"],"end":140592211,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592211,"source":"dbSNP","seq_region_name":"7","id":"rs2130663172","clinical_significance":[]},{"id":"rs796694345","seq_region_name":"7","clinical_significance":[],"start":140592212,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G","T"],"end":140592212,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592212,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","-"],"end":140592212,"seq_region_name":"7","id":"rs1205361231","clinical_significance":[]},{"alleles":["TTTTTTTTTTTT","TTTTTTTTTT","TTTTTTTTTTT","TTTTTTTTTTTTT","TTTTTTTTTTTTTT","TTTTTTTTTTTTTTT"],"end":140592224,"strand":1,"feature_type":"variation","start":140592213,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs576837816","clinical_significance":[]},{"alleles":["-","C","G"],"end":140592213,"feature_type":"variation","strand":1,"source":"dbSNP","start":140592214,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799085342"},{"id":"rs1204353119","seq_region_name":"7","clinical_significance":[],"end":140592216,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140592216,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs946587147","feature_type":"variation","strand":1,"alleles":["-","A"],"end":140592216,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592217},{"clinical_significance":[],"seq_region_name":"7","id":"rs867165281","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592217,"feature_type":"variation","strand":1,"end":140592217,"alleles":["T","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1229700035","end":140592217,"alleles":["-","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140592218,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140592218,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140592218,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1276363820"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592219,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["-","A"],"end":140592218,"id":"rs1313791911","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592219,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140592219,"seq_region_name":"7","id":"rs770684060","clinical_significance":[]},{"id":"rs1263229049","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592225,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140592225},{"seq_region_name":"7","id":"rs1175819887","clinical_significance":[],"start":140592229,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G","T"],"end":140592229,"strand":1,"feature_type":"variation"},{"end":140592230,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140592230,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1306995962"},{"seq_region_name":"7","id":"rs1250317603","clinical_significance":[],"start":140592231,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140592231,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1350272563","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592237,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140592237},{"end":140592238,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140592238,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs571342149","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs374647767","feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140592245,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592245},{"id":"rs1383389427","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592246,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140592246},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799087249","end":140592247,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140592247,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140592252,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592252,"source":"dbSNP","seq_region_name":"7","id":"rs1585711423","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1424109418","feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140592256,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592256},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592259,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140592259,"seq_region_name":"7","id":"rs1003371432","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1478533492","alleles":["G","T"],"end":140592263,"feature_type":"variation","strand":1,"source":"dbSNP","start":140592263,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs187108265","clinical_significance":[],"start":140592269,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140592269,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"start":140592270,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140592270,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","id":"rs895203145","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799088049","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592273,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140592273},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592277,"source":"dbSNP","strand":1,"feature_type":"variation","end":140592277,"alleles":["G","T"],"id":"rs1489752555","seq_region_name":"7","clinical_significance":[]},{"end":140592280,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140592280,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799088271"},{"feature_type":"variation","strand":1,"alleles":["C","-"],"end":140592282,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592282,"clinical_significance":[],"seq_region_name":"7","id":"rs2130663411"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585711498","source":"dbSNP","start":140592284,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140592284,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1799088513","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140592292,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592292,"source":"dbSNP"},{"start":140592293,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C","G"],"end":140592293,"strand":1,"feature_type":"variation","id":"rs1297384172","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140592294,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140592294,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799088770"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1290390844","alleles":["CCTCCTC","CCTC"],"end":140592300,"feature_type":"variation","strand":1,"source":"dbSNP","start":140592294,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1216615117","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592295,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140592295},{"strand":1,"feature_type":"variation","end":140592297,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592297,"source":"dbSNP","seq_region_name":"7","id":"rs946388695","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585711538","feature_type":"variation","strand":1,"end":140592300,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592300},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592301,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140592301,"seq_region_name":"7","id":"rs1799089378","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799089496","source":"dbSNP","start":140592303,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140592303,"alleles":["T","C"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140592306,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140592306,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799089610"},{"seq_region_name":"7","id":"rs1355245509","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592309,"source":"dbSNP","strand":1,"feature_type":"variation","end":140592309,"alleles":["C","T"]},{"clinical_significance":[],"id":"rs1281998439","seq_region_name":"7","end":140592311,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140592311,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140592313,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592313,"clinical_significance":[],"seq_region_name":"7","id":"rs148638814"},{"seq_region_name":"7","id":"rs1799089992","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140592320,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592320,"source":"dbSNP"},{"id":"rs1397646944","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140592326,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592326,"source":"dbSNP"},{"seq_region_name":"7","id":"rs2130663515","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592327,"source":"dbSNP","strand":1,"feature_type":"variation","end":140592327,"alleles":["C","A"]},{"seq_region_name":"7","id":"rs1310506740","clinical_significance":[],"alleles":["T","C"],"end":140592330,"strand":1,"feature_type":"variation","start":140592330,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs902256529","seq_region_name":"7","source":"dbSNP","start":140592331,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140592331,"alleles":["C","T"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140592332,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140592332,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1228538712"},{"id":"rs1299227988","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140592333,"alleles":["A","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592333,"source":"dbSNP"},{"source":"dbSNP","start":140592334,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140592334,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1434567303"},{"clinical_significance":[],"id":"rs1478777445","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140592344,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592344},{"end":140592349,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140592349,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1203447946","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140592351,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592351,"source":"dbSNP","seq_region_name":"7","id":"rs1345190678","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140592352,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592352,"clinical_significance":[],"seq_region_name":"7","id":"rs1799091095"},{"strand":1,"feature_type":"variation","end":140592355,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592355,"source":"dbSNP","id":"rs1299041463","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140592356,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592356,"source":"dbSNP","seq_region_name":"7","id":"rs1799091461","clinical_significance":[]},{"start":140592357,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140592357,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1017322062","clinical_significance":[]},{"start":140592359,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140592359,"alleles":["A","C"],"strand":1,"feature_type":"variation","id":"rs1585711712","seq_region_name":"7","clinical_significance":[]},{"id":"rs2130663622","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592361,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140592361},{"clinical_significance":[],"seq_region_name":"7","id":"rs1358727396","source":"dbSNP","start":140592362,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140592362,"alleles":["A","G"],"feature_type":"variation","strand":1},{"alleles":["T","C"],"end":140592363,"strand":1,"feature_type":"variation","start":140592363,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1158967805","seq_region_name":"7","clinical_significance":[]},{"start":140592364,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140592364,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1003256894","clinical_significance":[]},{"source":"dbSNP","start":140592373,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TTTTTT","TTTTTTT"],"end":140592378,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs962696033","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs60376704","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592378,"feature_type":"variation","strand":1,"end":140592378,"alleles":["T","A","C"]},{"end":140592379,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140592379,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs113100699"},{"seq_region_name":"7","id":"rs1799092837","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592382,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140592382},{"strand":1,"feature_type":"variation","alleles":["TTTT","TTT"],"end":140592386,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592383,"source":"dbSNP","seq_region_name":"7","id":"rs1170017071","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592387,"feature_type":"variation","strand":1,"end":140592387,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799093204"},{"id":"rs1359470640","seq_region_name":"7","clinical_significance":[],"start":140592388,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A","G"],"end":140592388,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1012192647","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592393,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140592393},{"seq_region_name":"7","id":"rs555521171","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140592396,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592396,"source":"dbSNP"},{"source":"dbSNP","start":140592397,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140592396,"alleles":["-","TT"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799094017","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1488959414","source":"dbSNP","start":140592402,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C","G"],"end":140592402,"feature_type":"variation","strand":1},{"start":140592412,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140592412,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1258472507","clinical_significance":[]},{"id":"rs952852229","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140592413,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592413,"source":"dbSNP"},{"end":140592414,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140592414,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799094834"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592419,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140592419,"seq_region_name":"7","id":"rs986915450","clinical_significance":[]},{"seq_region_name":"7","id":"rs572996078","clinical_significance":[],"start":140592420,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G","T"],"end":140592420,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1322578176","source":"dbSNP","start":140592426,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140592426,"alleles":["T","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1279019540","clinical_significance":[],"end":140592427,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140592427,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140592428,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592428,"source":"dbSNP","seq_region_name":"7","id":"rs911415984","clinical_significance":[]},{"start":140592431,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140592431,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799095923","clinical_significance":[]},{"start":140592432,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140592432,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs142144829","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592438,"source":"dbSNP","strand":1,"feature_type":"variation","end":140592438,"alleles":["C","G","T"],"seq_region_name":"7","id":"rs761581381","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592439,"feature_type":"variation","strand":1,"end":140592439,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs976775143"},{"seq_region_name":"7","id":"rs1799096459","clinical_significance":[],"start":140592440,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140592440,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140592442,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592442,"clinical_significance":[],"seq_region_name":"7","id":"rs1174591401"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592443,"source":"dbSNP","strand":1,"feature_type":"variation","end":140592443,"alleles":["C","T"],"seq_region_name":"7","id":"rs558815074","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592444,"feature_type":"variation","strand":1,"end":140592444,"alleles":["G","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs151206073"},{"source":"dbSNP","start":140592445,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140592445,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs544218833"},{"alleles":["C","A"],"end":140592452,"strand":1,"feature_type":"variation","start":140592452,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1799097128","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","G"],"end":140592453,"feature_type":"variation","strand":1,"source":"dbSNP","start":140592453,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs531448597","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140592454,"alleles":["G","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592454,"clinical_significance":[],"seq_region_name":"7","id":"rs1235924221"},{"end":140592456,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140592456,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1259038337","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","T"],"end":140592457,"strand":1,"feature_type":"variation","start":140592457,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1799097635","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs954193294","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140592467,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592467,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799097852","clinical_significance":[],"strand":1,"feature_type":"variation","end":140592468,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592468,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799097957","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["CCC","CC"],"end":140592470,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592468,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs985702468","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140592469,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592469},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592471,"feature_type":"variation","strand":1,"end":140592471,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799098162"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592472,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140592472,"id":"rs1239075582","seq_region_name":"7","clinical_significance":[]},{"id":"rs769373220","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140592474,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592474,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs946412534","source":"dbSNP","start":140592475,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140592475,"alleles":["T","G"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140592476,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592476,"source":"dbSNP","seq_region_name":"7","id":"rs1042057140","clinical_significance":[]},{"start":140592477,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140592477,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799098750","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130663948","end":140592479,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140592479,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140592480,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140592480,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799098857"},{"alleles":["A","T"],"end":140592487,"strand":1,"feature_type":"variation","start":140592487,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1209977376","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799099080","clinical_significance":[],"end":140592488,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140592488,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1249906169","clinical_significance":[],"start":140592489,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140592489,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs562494764","seq_region_name":"7","source":"dbSNP","start":140592491,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140592491,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs939097768","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592492,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140592492},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799099592","source":"dbSNP","start":140592493,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140592493,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592494,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140592494,"seq_region_name":"7","id":"rs1799099699","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799099888","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592496,"source":"dbSNP","strand":1,"feature_type":"variation","end":140592496,"alleles":["C","A"]},{"clinical_significance":[],"id":"rs1799099999","seq_region_name":"7","end":140592502,"alleles":["CCACCAC","CCACCACCAC"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140592496,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1295129680","feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140592499,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592499},{"source":"dbSNP","start":140592501,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140592501,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1228904150"},{"clinical_significance":[],"id":"rs1426178693","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592502,"feature_type":"variation","strand":1,"end":140592502,"alleles":["C","T"]},{"id":"rs140399161","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140592503,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592503,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140592505,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592505,"source":"dbSNP","seq_region_name":"7","id":"rs1056678198","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130664064","clinical_significance":[],"end":140592506,"alleles":["-","GGACCACCT"],"strand":1,"feature_type":"variation","start":140592507,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs894994640","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592509,"source":"dbSNP","strand":1,"feature_type":"variation","end":140592509,"alleles":["C","A"]},{"seq_region_name":"7","id":"rs2130664084","clinical_significance":[],"start":140592509,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140592509,"alleles":["C","CATTATTTCTACAGCCTACATAAATGTCAGGGACATCAGTCC","CATTATTTCTACAGCCTACATAAATGTCAGGGACATCAGTCCTCCC"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1333854493","alleles":["A","G","T"],"end":140592511,"feature_type":"variation","strand":1,"source":"dbSNP","start":140592511,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592512,"feature_type":"variation","strand":1,"end":140592512,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799100956"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592513,"feature_type":"variation","strand":1,"end":140592513,"alleles":["T","C"],"clinical_significance":[],"id":"rs1799101061","seq_region_name":"7"},{"end":140592514,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140592514,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1466861588","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1012714776","feature_type":"variation","strand":1,"end":140592518,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592518},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592519,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140592519,"seq_region_name":"7","id":"rs895006620","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592520,"source":"dbSNP","strand":1,"feature_type":"variation","end":140592524,"alleles":["TTTTT","TTTT"],"id":"rs1799101426","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1423845474","feature_type":"variation","strand":1,"end":140592521,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592521},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592523,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140592523,"seq_region_name":"7","id":"rs371678425","clinical_significance":[]},{"alleles":["G","A"],"end":140592529,"feature_type":"variation","strand":1,"source":"dbSNP","start":140592529,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1181646994"},{"feature_type":"variation","strand":1,"end":140592531,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592531,"clinical_significance":[],"id":"rs1049484326","seq_region_name":"7"},{"start":140592533,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140592533,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1238549388","clinical_significance":[]},{"alleles":["G","C"],"end":140592535,"feature_type":"variation","strand":1,"source":"dbSNP","start":140592535,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1342870291"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592536,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140592536,"seq_region_name":"7","id":"rs1479542646","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140592541,"alleles":["TTTT","TTT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592538,"clinical_significance":[],"seq_region_name":"7","id":"rs1799102801"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592542,"source":"dbSNP","strand":1,"feature_type":"variation","end":140592553,"alleles":["GCCATGTTGGGC","GC"],"seq_region_name":"7","id":"rs1250921136","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799103198","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140592543,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592543,"source":"dbSNP"},{"id":"rs1799103357","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592544,"source":"dbSNP","strand":1,"feature_type":"variation","end":140592544,"alleles":["C","T"]},{"strand":1,"feature_type":"variation","end":140592546,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592546,"source":"dbSNP","seq_region_name":"7","id":"rs2130664219","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140592547,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592547,"source":"dbSNP","seq_region_name":"7","id":"rs887699672","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140592551,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592551,"clinical_significance":[],"id":"rs1313068225","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799103953","clinical_significance":[],"strand":1,"feature_type":"variation","end":140592553,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592553,"source":"dbSNP"},{"source":"dbSNP","start":140592565,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140592565,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799104135"},{"clinical_significance":[],"id":"rs190357063","seq_region_name":"7","alleles":["A","C","T"],"end":140592567,"feature_type":"variation","strand":1,"source":"dbSNP","start":140592567,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs2130664264","clinical_significance":[],"strand":1,"feature_type":"variation","end":140592569,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592569,"source":"dbSNP"},{"source":"dbSNP","start":140592574,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140592574,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799104599","seq_region_name":"7"},{"source":"dbSNP","start":140592575,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140592575,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1025627941"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140592576,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592576,"clinical_significance":[],"seq_region_name":"7","id":"rs1312106483"},{"end":140592579,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140592579,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799105194"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799105398","feature_type":"variation","strand":1,"end":140592581,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592581},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140592587,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592587,"clinical_significance":[],"seq_region_name":"7","id":"rs763368044"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592588,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140592588,"clinical_significance":[],"seq_region_name":"7","id":"rs1389974629"},{"seq_region_name":"7","id":"rs1396261017","clinical_significance":[],"start":140592590,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140592590,"alleles":["G","A","C"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592592,"source":"dbSNP","strand":1,"feature_type":"variation","end":140592592,"alleles":["C","G","T"],"seq_region_name":"7","id":"rs1799106181","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592594,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140592594,"clinical_significance":[],"seq_region_name":"7","id":"rs1015608219"},{"id":"rs1458132003","seq_region_name":"7","clinical_significance":[],"start":140592596,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140592596,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592596,"source":"dbSNP","strand":1,"feature_type":"variation","end":140592598,"alleles":["CCC","CC"],"id":"rs200477196","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592597,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140592597,"seq_region_name":"7","id":"rs1366871265","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs112671241","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592598,"feature_type":"variation","strand":1,"end":140592597,"alleles":["-","T","TT","TTT","TTTT"]},{"start":140592598,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140592598,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs57591156","clinical_significance":[]},{"end":140592598,"alleles":["C","TTT"],"strand":1,"feature_type":"variation","start":140592598,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs373854709","clinical_significance":[]},{"id":"rs745373615","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["-","CT"],"end":140592598,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592599,"source":"dbSNP"},{"end":140592609,"alleles":["TTTTTTTTTTT","TTTTTTTTTT","TTTTTTTTTTTT","TTTTTTTTTTTTT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140592599,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs59623254","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1249605553","alleles":["T","C"],"end":140592602,"feature_type":"variation","strand":1,"source":"dbSNP","start":140592602,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1018830030","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592606,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140592606},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592608,"source":"dbSNP","strand":1,"feature_type":"variation","end":140592608,"alleles":["T","C"],"id":"rs1799107747","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140592609,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140592609,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1489620489","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592610,"source":"dbSNP","strand":1,"feature_type":"variation","end":140592610,"alleles":["C","A","T"],"seq_region_name":"7","id":"rs1402768401","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140592611,"alleles":["T","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592611,"source":"dbSNP","seq_region_name":"7","id":"rs2130664443","clinical_significance":[]},{"alleles":["TTTTTTT","TTTTTT"],"end":140592617,"strand":1,"feature_type":"variation","start":140592611,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1563164791","clinical_significance":[]},{"alleles":["T","C"],"end":140592612,"feature_type":"variation","strand":1,"source":"dbSNP","start":140592612,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1281755442"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799108336","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592617,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140592617},{"strand":1,"feature_type":"variation","end":140592618,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592618,"source":"dbSNP","seq_region_name":"7","id":"rs1323283365","clinical_significance":[]},{"source":"dbSNP","start":140592622,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140592622,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1354522838"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585712641","feature_type":"variation","strand":1,"end":140592623,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592623},{"clinical_significance":[],"id":"rs1315166259","seq_region_name":"7","end":140592626,"alleles":["AGAG","AG"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140592623,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140592626,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592626,"clinical_significance":[],"id":"rs1215120448","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592627,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140592627,"seq_region_name":"7","id":"rs964252260","clinical_significance":[]},{"end":140592628,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140592628,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs527907368","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592629,"source":"dbSNP","strand":1,"feature_type":"variation","end":140592629,"alleles":["T","G"],"seq_region_name":"7","id":"rs1799109233","clinical_significance":[]},{"source":"dbSNP","start":140592630,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C","T"],"end":140592630,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1386981786"},{"seq_region_name":"7","id":"rs1300918055","clinical_significance":[],"alleles":["C","G"],"end":140592634,"strand":1,"feature_type":"variation","start":140592634,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["T","G"],"end":140592637,"strand":1,"feature_type":"variation","start":140592637,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799109552","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140592638,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592638,"clinical_significance":[],"seq_region_name":"7","id":"rs182758143"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592639,"source":"dbSNP","strand":1,"feature_type":"variation","end":140592639,"alleles":["G","A"],"id":"rs1197620292","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","T"],"end":140592641,"strand":1,"feature_type":"variation","start":140592641,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1799109886","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs187403957","end":140592647,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140592647,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs967820242","seq_region_name":"7","clinical_significance":[],"end":140592648,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140592648,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1799110265","clinical_significance":[],"start":140592649,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140592649,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140592650,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592650,"source":"dbSNP","id":"rs1472802870","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs954243021","feature_type":"variation","strand":1,"end":140592654,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592654},{"seq_region_name":"7","id":"rs1799110604","clinical_significance":[],"start":140592660,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140592660,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs985642446","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592662,"source":"dbSNP","strand":1,"feature_type":"variation","end":140592662,"alleles":["C","T"]},{"id":"rs1799110823","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592663,"source":"dbSNP","strand":1,"feature_type":"variation","end":140592663,"alleles":["G","A"]},{"id":"rs771309392","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140592665,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592665,"source":"dbSNP"},{"end":140592670,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140592670,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs915354073","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs968337964","feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140592671,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592671},{"seq_region_name":"7","id":"rs1198998785","clinical_significance":[],"start":140592675,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140592675,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs978723018","clinical_significance":[],"strand":1,"feature_type":"variation","end":140592678,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592678,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1585712858","seq_region_name":"7","source":"dbSNP","start":140592680,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140592680,"alleles":["A","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs939221895","end":140592682,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140592682,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs923650930","clinical_significance":[],"alleles":["C","T"],"end":140592685,"strand":1,"feature_type":"variation","start":140592685,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140592686,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592686,"source":"dbSNP","id":"rs1203880132","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs550598948","source":"dbSNP","start":140592687,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140592687,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs568831994","clinical_significance":[],"end":140592688,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140592688,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1351171108","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592690,"source":"dbSNP","strand":1,"feature_type":"variation","end":140592690,"alleles":["C","T"]},{"end":140592695,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140592695,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799112237","seq_region_name":"7"},{"alleles":["T","G"],"end":140592696,"strand":1,"feature_type":"variation","start":140592696,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1585712926","seq_region_name":"7","clinical_significance":[]},{"start":140592698,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140592698,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1422294598","clinical_significance":[]},{"id":"rs1421208363","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592701,"source":"dbSNP","strand":1,"feature_type":"variation","end":140592701,"alleles":["G","A"]},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140592702,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592702,"source":"dbSNP","seq_region_name":"7","id":"rs1799112657","clinical_significance":[]},{"id":"rs1256952344","seq_region_name":"7","clinical_significance":[],"end":140592705,"alleles":["T","C","G"],"strand":1,"feature_type":"variation","start":140592705,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs192925964","end":140592707,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140592707,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140592708,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592708,"source":"dbSNP","seq_region_name":"7","id":"rs2130664725","clinical_significance":[]},{"id":"rs1464960808","seq_region_name":"7","clinical_significance":[],"start":140592709,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140592709,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140592710,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592710,"clinical_significance":[],"seq_region_name":"7","id":"rs1321879664"},{"seq_region_name":"7","id":"rs1345224864","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592711,"source":"dbSNP","strand":1,"feature_type":"variation","end":140592711,"alleles":["T","G"]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140592714,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592714,"clinical_significance":[],"seq_region_name":"7","id":"rs1280924655"},{"strand":1,"feature_type":"variation","end":140592716,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592716,"source":"dbSNP","seq_region_name":"7","id":"rs1403991450","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs548238263","end":140592717,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140592717,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1319785513","clinical_significance":[],"strand":1,"feature_type":"variation","end":140592724,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592724,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1380452222","clinical_significance":[],"start":140592726,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140592726,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs751851229","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592731,"source":"dbSNP","strand":1,"feature_type":"variation","end":140592731,"alleles":["C","G"]},{"source":"dbSNP","start":140592734,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140592734,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1384069713"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1173102484","source":"dbSNP","start":140592735,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140592735,"alleles":["G","T"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140592739,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140592739,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1470806547"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592740,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140592740,"id":"rs1171142441","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140592741,"alleles":["A","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592741,"source":"dbSNP","seq_region_name":"7","id":"rs1799114600","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140592744,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592744,"clinical_significance":[],"id":"rs947911515","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140592745,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592745,"source":"dbSNP","seq_region_name":"7","id":"rs1585713112","clinical_significance":[]},{"id":"rs1374855281","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140592748,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592748,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1038647216","seq_region_name":"7","end":140592759,"alleles":["TGCCACCATGCC","TGCC"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140592748,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799115280","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592749,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140592749},{"start":140592751,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140592751,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130664856","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140592753,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592753,"clinical_significance":[],"id":"rs916326078","seq_region_name":"7"},{"seq_region_name":"7","id":"rs566739865","clinical_significance":[],"alleles":["T","C"],"end":140592756,"strand":1,"feature_type":"variation","start":140592756,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140592758,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592758,"clinical_significance":[],"seq_region_name":"7","id":"rs1799115645"},{"alleles":["T","C"],"end":140592764,"strand":1,"feature_type":"variation","start":140592764,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799115776","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799115892","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592773,"source":"dbSNP","strand":1,"feature_type":"variation","end":140592773,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs994234212","alleles":["T","A","G"],"end":140592776,"feature_type":"variation","strand":1,"source":"dbSNP","start":140592776,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1799116190","seq_region_name":"7","source":"dbSNP","start":140592781,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140592781,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1446507043","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140592787,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592787,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1257416911","source":"dbSNP","start":140592789,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140592789,"alleles":["A","-"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592790,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140592790,"id":"rs1585713191","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799116609","alleles":["G","C"],"end":140592791,"feature_type":"variation","strand":1,"source":"dbSNP","start":140592791,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799116734","feature_type":"variation","strand":1,"end":140592794,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592794},{"alleles":["G","T"],"end":140592795,"strand":1,"feature_type":"variation","start":140592795,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1047025547","clinical_significance":[]},{"end":140592800,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140592800,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1799116959","seq_region_name":"7","clinical_significance":[]},{"end":140592802,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140592802,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs533760901"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592803,"source":"dbSNP","strand":1,"feature_type":"variation","end":140592803,"alleles":["A","G","T"],"seq_region_name":"7","id":"rs1799117243","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592806,"feature_type":"variation","strand":1,"end":140592806,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1725033187"},{"strand":1,"feature_type":"variation","end":140592813,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592813,"source":"dbSNP","seq_region_name":"7","id":"rs567610796","clinical_significance":[]},{"start":140592817,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140592817,"alleles":["G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799117495","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592819,"source":"dbSNP","strand":1,"feature_type":"variation","end":140592819,"alleles":["T","G"],"seq_region_name":"7","id":"rs1585713221","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799117722","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140592823,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592823,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs10244607","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592826,"feature_type":"variation","strand":1,"end":140592826,"alleles":["C","A","T"]},{"id":"rs1004820062","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140592828,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592828,"source":"dbSNP"},{"source":"dbSNP","start":140592830,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140592830,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1223774153"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140592834,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592834,"source":"dbSNP","seq_region_name":"7","id":"rs1318238060","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140592836,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592836,"source":"dbSNP","seq_region_name":"7","id":"rs1036669855","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799118591","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592839,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140592839},{"start":140592840,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140592840,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1563164981","clinical_significance":[]},{"end":140592841,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140592841,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs767887230","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","A"],"end":140592843,"strand":1,"feature_type":"variation","start":140592843,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1361684425","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799119142","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592848,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140592848},{"seq_region_name":"7","id":"rs1799119257","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592849,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140592849},{"source":"dbSNP","start":140592851,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140592851,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799119374"},{"source":"dbSNP","start":140592852,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140592852,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799119497"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799119623","feature_type":"variation","strand":1,"end":140592854,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592854},{"source":"dbSNP","start":140592857,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["CCCCCC","CCCCC"],"end":140592862,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1563164992","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140592858,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592858,"clinical_significance":[],"id":"rs1220459924","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1291345831","clinical_significance":[],"end":140592859,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140592859,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs998132052","source":"dbSNP","start":140592860,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140592860,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592861,"feature_type":"variation","strand":1,"alleles":["C","A","G","T"],"end":140592861,"clinical_significance":[],"seq_region_name":"7","id":"rs269240"},{"source":"dbSNP","start":140592862,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140592862,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799120471"},{"seq_region_name":"7","id":"rs1799120588","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592863,"source":"dbSNP","strand":1,"feature_type":"variation","end":140592865,"alleles":["AAA","AA"]},{"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140592869,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592869,"source":"dbSNP","seq_region_name":"7","id":"rs1799120702","clinical_significance":[]},{"seq_region_name":"7","id":"rs1184038527","clinical_significance":[],"end":140592879,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140592879,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140592880,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140592880,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799120964"},{"end":140592885,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140592885,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs900122212"},{"clinical_significance":[],"id":"rs1335912219","seq_region_name":"7","source":"dbSNP","start":140592887,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140592887,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1466337182","alleles":["C","T"],"end":140592888,"feature_type":"variation","strand":1,"source":"dbSNP","start":140592888,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs889869409","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140592889,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592889,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140592890,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592890,"source":"dbSNP","seq_region_name":"7","id":"rs1563165030","clinical_significance":[]},{"seq_region_name":"7","id":"rs1011734278","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592892,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140592892},{"strand":1,"feature_type":"variation","end":140592896,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592896,"source":"dbSNP","id":"rs1166386473","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs570613318","end":140592898,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140592898,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140592899,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140592899,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs537905758","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140592901,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592901,"source":"dbSNP","id":"rs185508914","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs35489843","seq_region_name":"7","end":140592903,"alleles":["CC","CCC"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140592902,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1022476293","seq_region_name":"7","clinical_significance":[],"end":140592903,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140592903,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1799122534","clinical_significance":[],"strand":1,"feature_type":"variation","end":140592904,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592904,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1185938762","alleles":["C","T"],"end":140592905,"feature_type":"variation","strand":1,"source":"dbSNP","start":140592905,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1021827157","alleles":["C","G","T"],"end":140592906,"feature_type":"variation","strand":1,"source":"dbSNP","start":140592906,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1199590748","alleles":["A","G"],"end":140592908,"feature_type":"variation","strand":1,"source":"dbSNP","start":140592908,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140592911,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592911,"source":"dbSNP","seq_region_name":"7","id":"rs1799123021","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799123166","clinical_significance":[],"start":140592913,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140592913,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1439931443","clinical_significance":[],"strand":1,"feature_type":"variation","end":140592915,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592915,"source":"dbSNP"},{"id":"rs1182439033","seq_region_name":"7","clinical_significance":[],"end":140592918,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140592918,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1799123492","clinical_significance":[],"end":140592924,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140592924,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1274614303","end":140592925,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140592925,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140592928,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592928,"clinical_significance":[],"seq_region_name":"7","id":"rs967766551"},{"source":"dbSNP","start":140592935,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140592935,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1338146226","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1284329795","seq_region_name":"7","source":"dbSNP","start":140592947,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140592947,"alleles":["A","G"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140592948,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592948,"clinical_significance":[],"id":"rs1799124130","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592949,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140592949,"clinical_significance":[],"seq_region_name":"7","id":"rs1248068274"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1415263545","source":"dbSNP","start":140592952,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","TT"],"end":140592952,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1757395256","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592953,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140592953},{"end":140592954,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140592954,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs776926084","clinical_significance":[]},{"alleles":["C","G"],"end":140592955,"strand":1,"feature_type":"variation","start":140592955,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799124600","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799124731","seq_region_name":"7","alleles":["C","T"],"end":140592956,"feature_type":"variation","strand":1,"source":"dbSNP","start":140592956,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1314304025","seq_region_name":"7","alleles":["C","T"],"end":140592959,"feature_type":"variation","strand":1,"source":"dbSNP","start":140592959,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140592962,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140592962,"alleles":["A","T"],"strand":1,"feature_type":"variation","id":"rs2130665370","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799124939","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592964,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140592964},{"start":140592966,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140592966,"alleles":["T","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1447176501","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs80094940","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140592967,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592967},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799125347","source":"dbSNP","start":140592969,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140592969,"alleles":["G","C"],"feature_type":"variation","strand":1},{"id":"rs1799125447","seq_region_name":"7","clinical_significance":[],"end":140592970,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140592970,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799125557","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592974,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140592974},{"clinical_significance":[],"id":"rs2130665419","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592976,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140592976},{"id":"rs1799125649","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592978,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140592978},{"alleles":["G","A"],"end":140592981,"strand":1,"feature_type":"variation","start":140592981,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs2130665443","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs978392782","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140592985,"source":"dbSNP","strand":1,"feature_type":"variation","end":140592985,"alleles":["C","G"]},{"start":140592986,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140592986,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1327061174","clinical_significance":[]},{"source":"dbSNP","start":140592994,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140592994,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799126003"},{"source":"dbSNP","start":140592995,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140592995,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs542184786","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140593005,"alleles":["GAAATGTGA","GA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140592997,"clinical_significance":[],"seq_region_name":"7","id":"rs1391524484"},{"seq_region_name":"7","id":"rs1799126326","clinical_significance":[],"start":140593001,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140593001,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1585713689","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593011,"feature_type":"variation","strand":1,"end":140593011,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs777823968","end":140593014,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140593014,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140593016,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140593016,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799126694","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799126803","source":"dbSNP","start":140593024,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140593024,"alleles":["T","A"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140593025,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593025,"clinical_significance":[],"seq_region_name":"7","id":"rs1799126903"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593026,"feature_type":"variation","strand":1,"end":140593026,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs369454260"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593030,"source":"dbSNP","strand":1,"feature_type":"variation","end":140593030,"alleles":["C","T"],"seq_region_name":"7","id":"rs28678462","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799127270","source":"dbSNP","start":140593031,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140593031,"alleles":["C","T"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140593036,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593036,"clinical_significance":[],"seq_region_name":"7","id":"rs1179837461"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593038,"feature_type":"variation","strand":1,"end":140593038,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1331276202"},{"start":140593043,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140593043,"alleles":["T","A"],"strand":1,"feature_type":"variation","id":"rs1353191922","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs146542798","feature_type":"variation","strand":1,"end":140593044,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593044},{"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140593053,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593053,"clinical_significance":[],"id":"rs1799127815","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["TTTTTTTT","TTTTTTT","TTTTTTTTT"],"end":140593060,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593053,"clinical_significance":[],"id":"rs112026672","seq_region_name":"7"},{"id":"rs188972614","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593059,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140593059},{"strand":1,"feature_type":"variation","end":140593060,"alleles":["T","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593060,"source":"dbSNP","seq_region_name":"7","id":"rs1356666281","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799128371","seq_region_name":"7","feature_type":"variation","strand":1,"end":140593063,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593063},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593064,"feature_type":"variation","strand":1,"end":140593064,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs532254703"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130665657","feature_type":"variation","strand":1,"end":140593065,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593065},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799128608","alleles":["G","A"],"end":140593070,"feature_type":"variation","strand":1,"source":"dbSNP","start":140593070,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["G","-"],"end":140593070,"feature_type":"variation","strand":1,"source":"dbSNP","start":140593070,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799128723","seq_region_name":"7"},{"seq_region_name":"7","id":"rs75645917","clinical_significance":[],"start":140593071,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A","C"],"end":140593071,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593076,"feature_type":"variation","strand":1,"end":140593076,"alleles":["G","A"],"clinical_significance":[],"id":"rs1563165157","seq_region_name":"7"},{"end":140593079,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140593079,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1375224166","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799129336","seq_region_name":"7","alleles":["A","G"],"end":140593090,"feature_type":"variation","strand":1,"source":"dbSNP","start":140593090,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1799129443","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593091,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140593091},{"clinical_significance":[],"seq_region_name":"7","id":"rs1314508358","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593092,"feature_type":"variation","strand":1,"end":140593092,"alleles":["A","G"]},{"feature_type":"variation","strand":1,"end":140593098,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593098,"clinical_significance":[],"id":"rs1799129700","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140593118,"alleles":["TGTG","TG"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593115,"clinical_significance":[],"seq_region_name":"7","id":"rs1563165167"},{"start":140593121,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140593122,"alleles":["AG","-"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799130017","clinical_significance":[]},{"id":"rs1441741502","seq_region_name":"7","clinical_significance":[],"start":140593123,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140593123,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593126,"feature_type":"variation","strand":1,"end":140593126,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs940504363"},{"feature_type":"variation","strand":1,"end":140593128,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593128,"clinical_significance":[],"seq_region_name":"7","id":"rs1585713930"},{"id":"rs73500413","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593132,"source":"dbSNP","strand":1,"feature_type":"variation","end":140593132,"alleles":["C","T"]},{"strand":1,"feature_type":"variation","end":140593133,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593133,"source":"dbSNP","seq_region_name":"7","id":"rs901765001","clinical_significance":[]},{"seq_region_name":"7","id":"rs933199609","clinical_significance":[],"alleles":["T","A","C"],"end":140593135,"strand":1,"feature_type":"variation","start":140593135,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593137,"feature_type":"variation","strand":1,"end":140593141,"alleles":["ACCAC","ACCACCAC"],"clinical_significance":[],"id":"rs1159748199","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1403003683","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593138,"feature_type":"variation","strand":1,"end":140593138,"alleles":["C","T"]},{"end":140593141,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140593141,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs746950961","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799131817","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593146,"source":"dbSNP","strand":1,"feature_type":"variation","end":140593146,"alleles":["A","C"]},{"seq_region_name":"7","id":"rs1799131970","clinical_significance":[],"alleles":["A","C"],"end":140593147,"strand":1,"feature_type":"variation","start":140593147,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1799132128","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593155,"source":"dbSNP","strand":1,"feature_type":"variation","end":140593161,"alleles":["TCTCTCT","TCT"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593156,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140593156,"id":"rs1585714006","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593158,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140593158,"clinical_significance":[],"seq_region_name":"7","id":"rs1799132439"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799132553","feature_type":"variation","strand":1,"end":140593163,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593163},{"seq_region_name":"7","id":"rs192700682","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140593167,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593167,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140593169,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593169,"source":"dbSNP","seq_region_name":"7","id":"rs572318695","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130665864","clinical_significance":[],"end":140593180,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140593180,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1244931274","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","-"],"end":140593183,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593183,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs548156340","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593187,"feature_type":"variation","strand":1,"end":140593187,"alleles":["C","T"]},{"clinical_significance":[],"id":"rs115224303","seq_region_name":"7","source":"dbSNP","start":140593188,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140593188,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140593189,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140593220,"alleles":["ACATCCCGCCTGCAAGTTTAATAAGTAAACAT","ACAT"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1216389293"},{"seq_region_name":"7","id":"rs1318727053","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140593190,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593190,"source":"dbSNP"},{"seq_region_name":"7","id":"rs527531835","clinical_significance":[],"end":140593193,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140593193,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140593195,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593195,"source":"dbSNP","seq_region_name":"7","id":"rs1022783919","clinical_significance":[]},{"alleles":["G","A"],"end":140593196,"feature_type":"variation","strand":1,"source":"dbSNP","start":140593196,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1450940830"},{"clinical_significance":[],"id":"rs1403382228","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","A"],"end":140593199,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593199},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140593200,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593200,"source":"dbSNP","id":"rs1165798836","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140593214,"alleles":["AAGTTTAATAAGT","AAGT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593202,"clinical_significance":[],"id":"rs1799134681","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1344942130","clinical_significance":[],"end":140593204,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140593204,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs904050611","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593205,"feature_type":"variation","strand":1,"end":140593205,"alleles":["T","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1433501340","source":"dbSNP","start":140593208,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140593208,"alleles":["A","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1409772395","source":"dbSNP","start":140593214,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140593214,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1335397075","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593219,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140593219},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593222,"source":"dbSNP","strand":1,"feature_type":"variation","end":140593222,"alleles":["C","A","T"],"id":"rs1000097702","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593223,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140593223,"clinical_significance":[],"seq_region_name":"7","id":"rs1415355209"},{"seq_region_name":"7","id":"rs1799135979","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140593226,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593226,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1431948051","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593228,"feature_type":"variation","strand":1,"end":140593228,"alleles":["A","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs768523047","alleles":["C","G","T"],"end":140593238,"feature_type":"variation","strand":1,"source":"dbSNP","start":140593238,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140593244,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593244,"source":"dbSNP","seq_region_name":"7","id":"rs1799136495","clinical_significance":[]},{"seq_region_name":"7","id":"rs1451152852","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140593245,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593245,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1585714226","clinical_significance":[],"alleles":["G","A","T"],"end":140593246,"strand":1,"feature_type":"variation","start":140593246,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593248,"feature_type":"variation","strand":1,"end":140593248,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799137058"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130666091","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140593253,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593253},{"seq_region_name":"7","id":"rs1479283860","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593253,"source":"dbSNP","strand":1,"feature_type":"variation","end":140593255,"alleles":["AAA","AA"]},{"alleles":["G","A"],"end":140593256,"strand":1,"feature_type":"variation","start":140593256,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs781149991","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140593257,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593257,"source":"dbSNP","seq_region_name":"7","id":"rs1031299683","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140593258,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593258,"clinical_significance":[],"seq_region_name":"7","id":"rs960952560"},{"clinical_significance":[],"seq_region_name":"7","id":"rs992378163","feature_type":"variation","strand":1,"end":140593259,"alleles":["G","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593259},{"source":"dbSNP","start":140593264,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140593264,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1486569041","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1023323033","clinical_significance":[],"start":140593266,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140593266,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140593275,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593275,"clinical_significance":[],"seq_region_name":"7","id":"rs1799138321"},{"seq_region_name":"7","id":"rs1030756570","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593281,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140593281},{"feature_type":"variation","strand":1,"end":140593282,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593282,"clinical_significance":[],"seq_region_name":"7","id":"rs1563165278"},{"end":140593289,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140593289,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1461577478","clinical_significance":[]},{"seq_region_name":"7","id":"rs1264827775","clinical_significance":[],"alleles":["G","C"],"end":140593292,"strand":1,"feature_type":"variation","start":140593292,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs969440095","clinical_significance":[],"strand":1,"feature_type":"variation","end":140593295,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593295,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs747737745","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593300,"feature_type":"variation","strand":1,"end":140593300,"alleles":["G","A"]},{"alleles":["G","A"],"end":140593303,"feature_type":"variation","strand":1,"source":"dbSNP","start":140593303,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799139108","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799139216","feature_type":"variation","strand":1,"end":140593306,"alleles":["AA","AAA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593305},{"strand":1,"feature_type":"variation","end":140593322,"alleles":["CTCAGCCTCA","CTCA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593313,"source":"dbSNP","id":"rs763499453","seq_region_name":"7","clinical_significance":[]},{"start":140593314,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140593314,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs991827847","clinical_significance":[]},{"start":140593324,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140593324,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs1799139736","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593332,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140593332,"seq_region_name":"7","id":"rs1799139912","clinical_significance":[]},{"id":"rs1023744108","seq_region_name":"7","clinical_significance":[],"end":140593333,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140593333,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799140248","alleles":["A","G"],"end":140593334,"feature_type":"variation","strand":1,"source":"dbSNP","start":140593334,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593335,"source":"dbSNP","strand":1,"feature_type":"variation","end":140593335,"alleles":["G","A"],"seq_region_name":"7","id":"rs1799140405","clinical_significance":[]},{"start":140593336,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140593336,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs115888279","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799140752","clinical_significance":[],"start":140593339,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140593339,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs570352894","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140593343,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593343},{"clinical_significance":[],"seq_region_name":"7","id":"rs908945375","alleles":["A","C","G","T"],"end":140593344,"feature_type":"variation","strand":1,"source":"dbSNP","start":140593344,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593345,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140593345,"clinical_significance":[],"id":"rs1799141405","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593349,"source":"dbSNP","strand":1,"feature_type":"variation","end":140593349,"alleles":["C","A"],"seq_region_name":"7","id":"rs1219559996","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593350,"feature_type":"variation","strand":1,"end":140593350,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs769639875"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593353,"feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140593353,"clinical_significance":[],"seq_region_name":"7","id":"rs929813723"},{"seq_region_name":"7","id":"rs982618519","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140593357,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593357,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1799142242","seq_region_name":"7","source":"dbSNP","start":140593361,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140593361,"alleles":["G","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1799142412","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593363,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140593363},{"source":"dbSNP","start":140593365,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140593365,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799142587"},{"clinical_significance":[],"id":"rs537645924","seq_region_name":"7","alleles":["A","G"],"end":140593371,"feature_type":"variation","strand":1,"source":"dbSNP","start":140593371,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130666357","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593374,"feature_type":"variation","strand":1,"end":140593374,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799142954","source":"dbSNP","start":140593380,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140593380,"alleles":["G","-"],"feature_type":"variation","strand":1},{"alleles":["G","C"],"end":140593383,"feature_type":"variation","strand":1,"source":"dbSNP","start":140593383,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799143078"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593385,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140593385,"clinical_significance":[],"seq_region_name":"7","id":"rs1429731659"},{"seq_region_name":"7","id":"rs1799143313","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593389,"source":"dbSNP","strand":1,"feature_type":"variation","end":140593389,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs1799143490","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593390,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140593390},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593392,"source":"dbSNP","strand":1,"feature_type":"variation","end":140593392,"alleles":["A","C"],"seq_region_name":"7","id":"rs2130666394","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140593396,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593396,"clinical_significance":[],"seq_region_name":"7","id":"rs1416818970"},{"strand":1,"feature_type":"variation","end":140593398,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593398,"source":"dbSNP","seq_region_name":"7","id":"rs1799143730","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799143893","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593400,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140593400},{"clinical_significance":[],"seq_region_name":"7","id":"rs1185838928","source":"dbSNP","start":140593403,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140593403,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1445228308","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593406,"source":"dbSNP","strand":1,"feature_type":"variation","end":140593406,"alleles":["A","G"]},{"end":140593408,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140593408,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1244741744","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799144380","clinical_significance":[],"alleles":["C","T"],"end":140593411,"strand":1,"feature_type":"variation","start":140593411,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1799144545","clinical_significance":[],"end":140593414,"alleles":["TTT","TT"],"strand":1,"feature_type":"variation","start":140593412,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140593421,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["GGGCG","G"],"end":140593425,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799144721","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1201470017","end":140593423,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140593423,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593424,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140593424,"clinical_significance":[],"seq_region_name":"7","id":"rs556266669"},{"seq_region_name":"7","id":"rs1252065069","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593425,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140593425},{"clinical_significance":[],"seq_region_name":"7","id":"rs1206933741","feature_type":"variation","strand":1,"end":140593429,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593429},{"alleles":["C","A","G"],"end":140593432,"feature_type":"variation","strand":1,"source":"dbSNP","start":140593432,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1305809822","seq_region_name":"7"},{"source":"dbSNP","start":140593433,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140593433,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs971874297"},{"seq_region_name":"7","id":"rs2130666499","clinical_significance":[],"start":140593436,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140593436,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1799145934","clinical_significance":[],"end":140593440,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140593440,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1385525922","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140593441,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593441,"source":"dbSNP"},{"source":"dbSNP","start":140593442,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140593442,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs116183116"},{"source":"dbSNP","start":140593451,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140593451,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs762577268","seq_region_name":"7"},{"alleles":["C","T"],"end":140593452,"strand":1,"feature_type":"variation","start":140593452,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs899844332","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1585714623","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593454,"feature_type":"variation","strand":1,"end":140593454,"alleles":["A","T"]},{"source":"dbSNP","start":140593455,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140593455,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1298361725"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799147221","end":140593457,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140593457,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1799147389","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593458,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140593458},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140593459,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593459,"clinical_significance":[],"seq_region_name":"7","id":"rs1799147508"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799147626","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593464,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140593464},{"start":140593466,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140593466,"strand":1,"feature_type":"variation","id":"rs1463245462","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140593469,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","G"],"end":140593469,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1352246780"},{"end":140593472,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140593472,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs183715016"},{"source":"dbSNP","start":140593473,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140593473,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585714684"},{"seq_region_name":"7","id":"rs1799148254","clinical_significance":[],"alleles":["G","A"],"end":140593475,"strand":1,"feature_type":"variation","start":140593475,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140593477,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593477,"clinical_significance":[],"seq_region_name":"7","id":"rs2130666597"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799148372","feature_type":"variation","strand":1,"end":140593483,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593483},{"id":"rs79121742","seq_region_name":"7","clinical_significance":[],"end":140593485,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140593485,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140593486,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140593486,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs6957901"},{"alleles":["T","C"],"end":140593487,"strand":1,"feature_type":"variation","start":140593487,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs540100187","clinical_significance":[]},{"start":140593488,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140593488,"alleles":["A","-"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799148739","clinical_significance":[]},{"id":"rs1443743015","seq_region_name":"7","clinical_significance":[],"alleles":["G","C","T"],"end":140593493,"strand":1,"feature_type":"variation","start":140593493,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140593494,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140593494,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799148984"},{"id":"rs1799149161","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593497,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140593497},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799149334","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593500,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140593500},{"source":"dbSNP","start":140593501,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140593501,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799149514","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593508,"feature_type":"variation","strand":1,"end":140593508,"alleles":["C","G","T"],"clinical_significance":[],"id":"rs903935876","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593509,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140593509,"id":"rs999579653","seq_region_name":"7","clinical_significance":[]},{"id":"rs2130666669","seq_region_name":"7","clinical_significance":[],"end":140593510,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140593510,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140593513,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140593513,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1179152712","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593514,"source":"dbSNP","strand":1,"feature_type":"variation","end":140593514,"alleles":["C","T"],"seq_region_name":"7","id":"rs1241189937","clinical_significance":[]},{"seq_region_name":"7","id":"rs1478174330","clinical_significance":[],"start":140593518,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140593518,"alleles":["T","G"],"strand":1,"feature_type":"variation"},{"alleles":["AAA","AA"],"end":140593532,"strand":1,"feature_type":"variation","start":140593530,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799150450","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140593533,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593533,"source":"dbSNP","seq_region_name":"7","id":"rs6947111","clinical_significance":[]},{"seq_region_name":"7","id":"rs576759899","clinical_significance":[],"alleles":["G","A"],"end":140593534,"strand":1,"feature_type":"variation","start":140593534,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["C","T"],"end":140593539,"strand":1,"feature_type":"variation","start":140593539,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs896629028","clinical_significance":[]},{"end":140593541,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140593541,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1799151090","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140593546,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593546,"source":"dbSNP","seq_region_name":"7","id":"rs1223239348","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799151317","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140593554,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593554,"source":"dbSNP"},{"start":140593559,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140593559,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1431970460","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799151563","clinical_significance":[],"end":140593564,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140593564,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593566,"feature_type":"variation","strand":1,"end":140593566,"alleles":["C","A","T"],"clinical_significance":[],"id":"rs572689571","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140593567,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593567,"source":"dbSNP","seq_region_name":"7","id":"rs1245937008","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593571,"feature_type":"variation","strand":1,"end":140593571,"alleles":["G","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130666778"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799151953","end":140593587,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140593587,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140593589,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140593589,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1317872141","seq_region_name":"7"},{"end":140593590,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140593590,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs544012560","seq_region_name":"7"},{"source":"dbSNP","start":140593590,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["GTAATCCTA","-"],"end":140593598,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1309680454"},{"end":140593594,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140593594,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1370638425","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799152682","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593600,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140593600},{"seq_region_name":"7","id":"rs1307042118","clinical_significance":[],"start":140593602,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140593602,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1799152931","clinical_significance":[],"start":140593603,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140593603,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1799153042","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593604,"source":"dbSNP","strand":1,"feature_type":"variation","end":140593604,"alleles":["T","C"]},{"start":140593605,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140593605,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","id":"rs1013769575","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1366935687","clinical_significance":[],"strand":1,"feature_type":"variation","end":140593613,"alleles":["TGATGA","TGA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593608,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1389411245","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140593612,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593612},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593616,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140593616,"seq_region_name":"7","id":"rs1799153505","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799153607","clinical_significance":[],"alleles":["C","A"],"end":140593617,"strand":1,"feature_type":"variation","start":140593617,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1161566257","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593622,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140593622},{"source":"dbSNP","start":140593627,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140593627,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1384029577"},{"seq_region_name":"7","id":"rs1023268648","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593628,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140593628},{"clinical_significance":[],"seq_region_name":"7","id":"rs1160931053","source":"dbSNP","start":140593632,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140593632,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140593634,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593634,"source":"dbSNP","seq_region_name":"7","id":"rs1799154476","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799154645","feature_type":"variation","strand":1,"end":140593635,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593635},{"seq_region_name":"7","id":"rs1417092476","clinical_significance":[],"alleles":["C","T"],"end":140593639,"strand":1,"feature_type":"variation","start":140593639,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140593645,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593645,"source":"dbSNP","seq_region_name":"7","id":"rs1585714980","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593647,"feature_type":"variation","strand":1,"alleles":["G","A","C","T"],"end":140593647,"clinical_significance":[],"seq_region_name":"7","id":"rs1563165405"},{"clinical_significance":[],"seq_region_name":"7","id":"rs562610039","end":140593648,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140593648,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799155503","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593649,"feature_type":"variation","strand":1,"end":140593649,"alleles":["T","C"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593650,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140593650,"clinical_significance":[],"id":"rs1316368137","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799155836","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593653,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140593653},{"seq_region_name":"7","id":"rs1490852050","clinical_significance":[],"alleles":["G","C"],"end":140593654,"strand":1,"feature_type":"variation","start":140593654,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1266926070","seq_region_name":"7","source":"dbSNP","start":140593657,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140593657,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140593658,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140593658,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs77022550"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593662,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140593662,"clinical_significance":[],"seq_region_name":"7","id":"rs1352120918"},{"clinical_significance":[],"id":"rs1437529238","seq_region_name":"7","feature_type":"variation","strand":1,"end":140593667,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593667},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799156843","alleles":["A","G"],"end":140593669,"feature_type":"variation","strand":1,"source":"dbSNP","start":140593669,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs995343736","end":140593675,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140593675,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["T","C"],"end":140593676,"feature_type":"variation","strand":1,"source":"dbSNP","start":140593676,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs141184622"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140593684,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593684,"clinical_significance":[],"id":"rs560051847","seq_region_name":"7"},{"end":140593685,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140593685,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1799157581","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593686,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140593686,"clinical_significance":[],"id":"rs1799157758","seq_region_name":"7"},{"seq_region_name":"7","id":"rs2130667055","clinical_significance":[],"start":140593689,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140593689,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799157930","feature_type":"variation","strand":1,"alleles":["CCC","CC"],"end":140593691,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593689},{"source":"dbSNP","start":140593693,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140593693,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1287281357"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1223792652","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593694,"feature_type":"variation","strand":1,"end":140593694,"alleles":["T","G"]},{"alleles":["T","C"],"end":140593695,"strand":1,"feature_type":"variation","start":140593695,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1346827058","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs951332832","feature_type":"variation","strand":1,"end":140593697,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593697},{"end":140593701,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140593701,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799158797"},{"seq_region_name":"7","id":"rs1006295542","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593704,"source":"dbSNP","strand":1,"feature_type":"variation","end":140593704,"alleles":["C","A","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1015891921","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593705,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140593705},{"start":140593721,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140593721,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","id":"rs962108045","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1451307179","source":"dbSNP","start":140593728,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140593728,"alleles":["T","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs767800934","clinical_significance":[],"end":140593734,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140593734,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1177391249","clinical_significance":[],"alleles":["G","C"],"end":140593738,"strand":1,"feature_type":"variation","start":140593738,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1799160368","clinical_significance":[],"start":140593741,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140593741,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1585715188","clinical_significance":[],"strand":1,"feature_type":"variation","end":140593749,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593749,"source":"dbSNP"},{"seq_region_name":"7","id":"rs965462980","clinical_significance":[],"strand":1,"feature_type":"variation","end":140593761,"alleles":["CCACCCACTTC","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593751,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799160693","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593753,"source":"dbSNP","strand":1,"feature_type":"variation","end":140593753,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs975912417","clinical_significance":[],"start":140593758,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140593758,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"id":"rs1288493954","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593760,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140593760},{"alleles":["C","G"],"end":140593763,"feature_type":"variation","strand":1,"source":"dbSNP","start":140593763,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs971758232"},{"clinical_significance":[],"seq_region_name":"7","id":"rs763484144","feature_type":"variation","strand":1,"end":140593772,"alleles":["CCCC","CCC"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593769},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593771,"source":"dbSNP","strand":1,"feature_type":"variation","end":140593771,"alleles":["C","T"],"seq_region_name":"7","id":"rs1563165480","clinical_significance":[]},{"id":"rs188228716","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140593772,"strand":1,"feature_type":"variation","start":140593772,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140593773,"alleles":["G","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593773,"clinical_significance":[],"seq_region_name":"7","id":"rs1260491926"},{"clinical_significance":[],"id":"rs1203930699","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140593775,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593775},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593776,"source":"dbSNP","strand":1,"feature_type":"variation","end":140593776,"alleles":["G","T"],"seq_region_name":"7","id":"rs552098240","clinical_significance":[]},{"alleles":["C","G"],"end":140593777,"strand":1,"feature_type":"variation","start":140593777,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1799162173","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1451803978","clinical_significance":[],"end":140593783,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140593783,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593788,"source":"dbSNP","strand":1,"feature_type":"variation","end":140593788,"alleles":["C","G","T"],"seq_region_name":"7","id":"rs1799162524","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593792,"source":"dbSNP","strand":1,"feature_type":"variation","end":140593792,"alleles":["G","A"],"seq_region_name":"7","id":"rs1799162762","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs921236824","source":"dbSNP","start":140593797,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140593797,"alleles":["C","T"],"feature_type":"variation","strand":1},{"id":"rs1799163123","seq_region_name":"7","clinical_significance":[],"start":140593799,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140593799,"strand":1,"feature_type":"variation"},{"end":140593803,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140593803,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585715339"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593804,"feature_type":"variation","strand":1,"end":140593804,"alleles":["C","G","T"],"clinical_significance":[],"id":"rs1799163473","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799163631","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593805,"feature_type":"variation","strand":1,"end":140593805,"alleles":["C","A","T"]},{"alleles":["CTCACTGTTTCTC","CTC"],"end":140593817,"feature_type":"variation","strand":1,"source":"dbSNP","start":140593805,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799163799","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1799163913","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593807,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140593807},{"seq_region_name":"7","id":"rs1585715348","clinical_significance":[],"end":140593809,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140593809,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140593810,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593810,"source":"dbSNP","seq_region_name":"7","id":"rs1799164165","clinical_significance":[]},{"alleles":["T","C"],"end":140593813,"feature_type":"variation","strand":1,"source":"dbSNP","start":140593813,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799164272"},{"seq_region_name":"7","id":"rs1203896113","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140593818,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593818,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799164521","end":140593820,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140593820,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1325155879","clinical_significance":[],"end":140593821,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140593821,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs764461680","source":"dbSNP","start":140593823,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140593823,"feature_type":"variation","strand":1},{"alleles":["G","A"],"end":140593824,"feature_type":"variation","strand":1,"source":"dbSNP","start":140593824,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799164988"},{"source":"dbSNP","start":140593829,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140593829,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1585715388","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1201215542","clinical_significance":[],"strand":1,"feature_type":"variation","end":140593831,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593831,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799165204","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593832,"source":"dbSNP","strand":1,"feature_type":"variation","end":140593832,"alleles":["G","A"]},{"end":140593833,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140593833,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1326532961","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585715419","end":140593834,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140593834,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs564016709","source":"dbSNP","start":140593835,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140593835,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1380506112","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140593838,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593838,"source":"dbSNP"},{"id":"rs1799165755","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140593845,"strand":1,"feature_type":"variation","start":140593845,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593849,"source":"dbSNP","strand":1,"feature_type":"variation","end":140593849,"alleles":["C","T"],"seq_region_name":"7","id":"rs1387618781","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799165974","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593856,"feature_type":"variation","strand":1,"end":140593856,"alleles":["A","T"]},{"seq_region_name":"7","id":"rs1799166156","clinical_significance":[],"start":140593858,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140593858,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"alleles":["T","C"],"end":140593860,"feature_type":"variation","strand":1,"source":"dbSNP","start":140593860,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1723347720"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593865,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140593865,"id":"rs1337224244","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799166855","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140593870,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593870,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs954528007","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593871,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140593871},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799167212","feature_type":"variation","strand":1,"end":140593873,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593873},{"source":"dbSNP","start":140593874,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140593874,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs986040489"},{"seq_region_name":"7","id":"rs1172237666","clinical_significance":[],"alleles":["G","C"],"end":140593875,"strand":1,"feature_type":"variation","start":140593875,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1475760607","seq_region_name":"7","source":"dbSNP","start":140593876,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140593876,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs924846390","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140593878,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593878},{"strand":1,"feature_type":"variation","end":140593881,"alleles":["T","A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593881,"source":"dbSNP","seq_region_name":"7","id":"rs910452563","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140593883,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593883,"clinical_significance":[],"seq_region_name":"7","id":"rs561529208"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593884,"source":"dbSNP","strand":1,"feature_type":"variation","end":140593884,"alleles":["C","A"],"seq_region_name":"7","id":"rs1449456276","clinical_significance":[]},{"source":"dbSNP","start":140593885,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140593885,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs942757752"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130667505","source":"dbSNP","start":140593887,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AAACAAGCAAATC","-"],"end":140593899,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593895,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140593895,"clinical_significance":[],"seq_region_name":"7","id":"rs1799168205"},{"seq_region_name":"7","id":"rs1244294183","clinical_significance":[],"end":140593896,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140593896,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140593897,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140593897,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1185746041","seq_region_name":"7"},{"end":140593898,"alleles":["T","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140593898,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs113149894"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593898,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","-"],"end":140593898,"seq_region_name":"7","id":"rs1460276573","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799168891","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593898,"feature_type":"variation","strand":1,"end":140593901,"alleles":["TCTT","T"]},{"seq_region_name":"7","id":"rs1364851095","clinical_significance":[],"end":140593900,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140593900,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs370516056","seq_region_name":"7","clinical_significance":[],"end":140593913,"alleles":["TTTTTTTTTTTTTT","TTTTTTTTTTT","TTTTTTTTTTTT","TTTTTTTTTTTTT","TTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT"],"strand":1,"feature_type":"variation","start":140593900,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs2130667607","seq_region_name":"7","feature_type":"variation","strand":1,"end":140593901,"alleles":["-","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593902},{"clinical_significance":[],"seq_region_name":"7","id":"rs1315662214","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593904,"feature_type":"variation","strand":1,"end":140593904,"alleles":["T","C"]},{"id":"rs1799169649","seq_region_name":"7","clinical_significance":[],"start":140593905,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140593905,"strand":1,"feature_type":"variation"},{"start":140593906,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140593906,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585715673","clinical_significance":[]},{"id":"rs549530429","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593911,"source":"dbSNP","strand":1,"feature_type":"variation","end":140593911,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs78824837","alleles":["C","T"],"end":140593914,"feature_type":"variation","strand":1,"source":"dbSNP","start":140593914,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593914,"feature_type":"variation","strand":1,"alleles":["C","-"],"end":140593914,"clinical_significance":[],"id":"rs1380348761","seq_region_name":"7"},{"source":"dbSNP","start":140593915,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TTTTTT","TTTTT","TTTTTTT"],"end":140593920,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1013300819"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593921,"feature_type":"variation","strand":1,"end":140593921,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1384438505"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1305205124","source":"dbSNP","start":140593923,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140593923,"alleles":["G","A","T"],"feature_type":"variation","strand":1},{"alleles":["GAGATGGAG","-"],"end":140593931,"feature_type":"variation","strand":1,"source":"dbSNP","start":140593923,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1406105966"},{"start":140593924,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140593924,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1343360231","clinical_significance":[]},{"seq_region_name":"7","id":"rs1404139636","clinical_significance":[],"start":140593926,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140593926,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1799171083","clinical_significance":[],"alleles":["T","C"],"end":140593927,"strand":1,"feature_type":"variation","start":140593927,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140593928,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140593928,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1799171255","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799171392","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140593929,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593929,"source":"dbSNP"},{"alleles":["G","C"],"end":140593931,"feature_type":"variation","strand":1,"source":"dbSNP","start":140593931,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1045216564"},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140593936,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593936,"clinical_significance":[],"seq_region_name":"7","id":"rs1799171686"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593937,"feature_type":"variation","strand":1,"end":140593937,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1443128220"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593941,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140593941,"clinical_significance":[],"seq_region_name":"7","id":"rs1237315022"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1337436414","source":"dbSNP","start":140593945,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140593945,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140593951,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140593951,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799172314"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799172457","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140593955,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593955},{"source":"dbSNP","start":140593956,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140593956,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs925275448"},{"id":"rs2130667777","seq_region_name":"7","clinical_significance":[],"start":140593960,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140593960,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1186383054","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593965,"source":"dbSNP","strand":1,"feature_type":"variation","end":140593965,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1799172921","clinical_significance":[],"alleles":["G","A"],"end":140593967,"strand":1,"feature_type":"variation","start":140593967,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140593969,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140593969,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799173073"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799173254","source":"dbSNP","start":140593972,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140593972,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593977,"feature_type":"variation","strand":1,"end":140593977,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799173415"},{"seq_region_name":"7","id":"rs568483766","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593981,"source":"dbSNP","strand":1,"feature_type":"variation","end":140593981,"alleles":["C","G","T"]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140593987,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593987,"clinical_significance":[],"seq_region_name":"7","id":"rs1052499442"},{"seq_region_name":"7","id":"rs896683033","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593988,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140593988},{"seq_region_name":"7","id":"rs1356442020","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140593989,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593989,"source":"dbSNP"},{"end":140593990,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140593990,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799174080","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140593991,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140593991,"clinical_significance":[],"id":"rs1799174258","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140593994,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593994,"source":"dbSNP","id":"rs1799174421","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140593996,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140593996,"source":"dbSNP","id":"rs995124562","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799174767","clinical_significance":[],"start":140593998,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140594002,"alleles":["TGGAT","T"],"strand":1,"feature_type":"variation"},{"alleles":["G","C"],"end":140593999,"feature_type":"variation","strand":1,"source":"dbSNP","start":140593999,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585715890"},{"seq_region_name":"7","id":"rs2130667871","clinical_significance":[],"end":140594001,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140594001,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594003,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140594003,"clinical_significance":[],"seq_region_name":"7","id":"rs1799175127"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594004,"feature_type":"variation","strand":1,"end":140594004,"alleles":["C","A"],"clinical_significance":[],"id":"rs1013750877","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1289167473","end":140594006,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140594006,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1045377968","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140594007,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594007,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594008,"source":"dbSNP","strand":1,"feature_type":"variation","end":140594008,"alleles":["C","T"],"id":"rs535896556","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","A","C"],"end":140594009,"feature_type":"variation","strand":1,"source":"dbSNP","start":140594009,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs4448176"},{"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140594015,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594015,"clinical_significance":[],"seq_region_name":"7","id":"rs1004099168"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594022,"source":"dbSNP","strand":1,"feature_type":"variation","end":140594022,"alleles":["C","A"],"seq_region_name":"7","id":"rs1016355383","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140594024,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594024,"clinical_significance":[],"seq_region_name":"7","id":"rs1337692138"},{"seq_region_name":"7","id":"rs1799177733","clinical_significance":[],"strand":1,"feature_type":"variation","end":140594025,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594025,"source":"dbSNP"},{"id":"rs1799177865","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140594030,"strand":1,"feature_type":"variation","start":140594030,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140594031,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140594031,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs28678005","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1409239466","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594032,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140594032},{"seq_region_name":"7","id":"rs780836651","clinical_significance":[],"alleles":["T","C"],"end":140594034,"strand":1,"feature_type":"variation","start":140594034,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs975314757","seq_region_name":"7","clinical_significance":[],"alleles":["G","C"],"end":140594040,"strand":1,"feature_type":"variation","start":140594040,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["G","C"],"end":140594041,"strand":1,"feature_type":"variation","start":140594041,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1423358741","clinical_significance":[]},{"start":140594044,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140594044,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585716045","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594054,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140594054,"seq_region_name":"7","id":"rs1030026264","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585716069","clinical_significance":[],"strand":1,"feature_type":"variation","end":140594055,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594055,"source":"dbSNP"},{"alleles":["C","T"],"end":140594057,"strand":1,"feature_type":"variation","start":140594057,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs539840358","clinical_significance":[]},{"alleles":["T","G"],"end":140594059,"strand":1,"feature_type":"variation","start":140594059,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799178914","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1159441267","feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140594060,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594060},{"seq_region_name":"7","id":"rs1180298258","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594061,"source":"dbSNP","strand":1,"feature_type":"variation","end":140594061,"alleles":["C","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594067,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140594067,"id":"rs1363244433","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1445343071","feature_type":"variation","strand":1,"end":140594069,"alleles":["A","AA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594069},{"source":"dbSNP","start":140594074,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140594074,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs954579763"},{"start":140594075,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140594075,"alleles":["T","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799179654","clinical_significance":[]},{"seq_region_name":"7","id":"rs1269039115","clinical_significance":[],"alleles":["G","T"],"end":140594080,"strand":1,"feature_type":"variation","start":140594080,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799179922","source":"dbSNP","start":140594081,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140594081,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799180051","feature_type":"variation","strand":1,"end":140594084,"alleles":["A","AGGGTAAA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594084},{"alleles":["T","A"],"end":140594086,"strand":1,"feature_type":"variation","start":140594086,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799180160","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130668100","clinical_significance":[],"alleles":["T","C"],"end":140594087,"strand":1,"feature_type":"variation","start":140594087,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799180261","source":"dbSNP","start":140594090,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["-","AAAA"],"end":140594089,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140594090,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594090,"source":"dbSNP","seq_region_name":"7","id":"rs1799180372","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs558518092","source":"dbSNP","start":140594091,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140594091,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs138760151","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594092,"feature_type":"variation","strand":1,"end":140594092,"alleles":["G","A"]},{"clinical_significance":[],"id":"rs1799180749","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594096,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140594096},{"id":"rs1799180883","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594097,"source":"dbSNP","strand":1,"feature_type":"variation","end":140594097,"alleles":["G","A"]},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140594099,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594099,"source":"dbSNP","seq_region_name":"7","id":"rs537659944","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799181119","alleles":["G","T"],"end":140594100,"feature_type":"variation","strand":1,"source":"dbSNP","start":140594100,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["T","G"],"end":140594102,"feature_type":"variation","strand":1,"source":"dbSNP","start":140594102,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs377181547"},{"seq_region_name":"7","id":"rs1224080911","clinical_significance":[],"end":140594106,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140594106,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594108,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140594108,"seq_region_name":"7","id":"rs978674470","clinical_significance":[]},{"id":"rs925295586","seq_region_name":"7","clinical_significance":[],"start":140594109,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140594109,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs148958098","source":"dbSNP","start":140594110,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140594110,"alleles":["G","A","T"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594111,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140594111,"clinical_significance":[],"id":"rs1799182166","seq_region_name":"7"},{"clinical_significance":[],"id":"rs2130668220","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594120,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140594120},{"alleles":["C","T"],"end":140594127,"strand":1,"feature_type":"variation","start":140594127,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs574455387","clinical_significance":[]},{"end":140594128,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140594128,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs757319421","clinical_significance":[]},{"source":"dbSNP","start":140594130,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140594130,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1389536733"},{"seq_region_name":"7","id":"rs1585716267","clinical_significance":[],"end":140594137,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140594137,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594140,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140594140,"seq_region_name":"7","id":"rs1585716280","clinical_significance":[]},{"clinical_significance":[],"id":"rs2130668273","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594141,"feature_type":"variation","strand":1,"end":140594141,"alleles":["C","A"]},{"clinical_significance":[],"id":"rs1477294608","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594142,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140594142},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799183536","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594144,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140594144},{"id":"rs1799183662","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140594149,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594149,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799183771","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140594150,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594150,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1319582266","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594152,"source":"dbSNP","strand":1,"feature_type":"variation","end":140594152,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799184014","source":"dbSNP","start":140594152,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["CCCCC","CCCCCC"],"end":140594156,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1306216807","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594155,"feature_type":"variation","strand":1,"end":140594155,"alleles":["C","A","G"]},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140594156,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594156,"source":"dbSNP","seq_region_name":"7","id":"rs1799184292","clinical_significance":[]},{"start":140594161,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140594161,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799184402","clinical_significance":[]},{"id":"rs1340494831","seq_region_name":"7","clinical_significance":[],"end":140594162,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140594162,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130668357","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594163,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140594163},{"alleles":["C","G"],"end":140594166,"feature_type":"variation","strand":1,"source":"dbSNP","start":140594166,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1156478962","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1247498405","clinical_significance":[],"strand":1,"feature_type":"variation","end":140594173,"alleles":["CCAAAATG","CCAAAATGCCAAAATG"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594166,"source":"dbSNP"},{"end":140594167,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140594167,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1799184893","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","C"],"end":140594169,"feature_type":"variation","strand":1,"source":"dbSNP","start":140594169,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799184997"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1472094766","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594174,"feature_type":"variation","strand":1,"end":140594174,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799185189","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594175,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140594175},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594177,"feature_type":"variation","strand":1,"end":140594177,"alleles":["G","A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1057506354"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594178,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140594178,"clinical_significance":[],"seq_region_name":"7","id":"rs1799185484"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799185572","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140594183,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594183},{"seq_region_name":"7","id":"rs1585716372","clinical_significance":[],"alleles":["A","G"],"end":140594185,"strand":1,"feature_type":"variation","start":140594185,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140594187,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594187,"source":"dbSNP","id":"rs369857081","seq_region_name":"7","clinical_significance":[]},{"id":"rs751457836","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140594188,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594188,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594189,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140594189,"clinical_significance":[],"seq_region_name":"7","id":"rs1799186089"},{"id":"rs1246011099","seq_region_name":"7","clinical_significance":[],"end":140594192,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140594192,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs373372376","source":"dbSNP","start":140594197,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140594197,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140594197,"alleles":["-","TTGCTGGACCATTTTGTTTTTTGAGATGGAGTCTTGCTCT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594198,"source":"dbSNP","seq_region_name":"7","id":"rs1585716442","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594198,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C","T"],"end":140594198,"seq_region_name":"7","id":"rs949406995","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594199,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140594199,"seq_region_name":"7","id":"rs781133438","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1324455957","source":"dbSNP","start":140594201,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140594201,"alleles":["C","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs200878125","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["CCC","CC"],"end":140594203,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594201,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1585716512","clinical_significance":[],"strand":1,"feature_type":"variation","end":140594201,"alleles":["-","TGGA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594202,"source":"dbSNP"},{"alleles":["C","A","G","T"],"end":140594203,"feature_type":"variation","strand":1,"source":"dbSNP","start":140594203,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs948896844"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594204,"feature_type":"variation","strand":1,"end":140594203,"alleles":["-","ATTTT"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585716535"},{"clinical_significance":[],"id":"rs1217499408","seq_region_name":"7","alleles":["G","A"],"end":140594204,"feature_type":"variation","strand":1,"source":"dbSNP","start":140594204,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["-","TTTTTTGAGATGGA"],"end":140594204,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594205,"clinical_significance":[],"seq_region_name":"7","id":"rs1585716564"},{"seq_region_name":"7","id":"rs1367036307","clinical_significance":[],"start":140594206,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140594206,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140594217,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594217,"clinical_significance":[],"id":"rs533037959","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799188154","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140594224,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594224,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140594227,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594227,"source":"dbSNP","id":"rs1799188281","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs755809600","clinical_significance":[],"end":140594228,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140594228,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs904938002","clinical_significance":[],"alleles":["T","C"],"end":140594229,"strand":1,"feature_type":"variation","start":140594229,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594233,"source":"dbSNP","strand":1,"feature_type":"variation","end":140594233,"alleles":["T","G"],"seq_region_name":"7","id":"rs931087391","clinical_significance":[]},{"source":"dbSNP","start":140594234,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140594234,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799188820"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1470512178","source":"dbSNP","start":140594238,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140594238,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1799189058","clinical_significance":[],"strand":1,"feature_type":"variation","end":140594239,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594239,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1406287788","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594240,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140594240},{"seq_region_name":"7","id":"rs942293574","clinical_significance":[],"strand":1,"feature_type":"variation","end":140594241,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594241,"source":"dbSNP"},{"alleles":["T","C"],"end":140594243,"strand":1,"feature_type":"variation","start":140594243,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs370493808","clinical_significance":[]},{"source":"dbSNP","start":140594245,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AAAAA","AAA"],"end":140594249,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799189596"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563165779","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594246,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140594246},{"start":140594249,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140594249,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1037939856","clinical_significance":[]},{"seq_region_name":"7","id":"rs184016443","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594251,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C","T"],"end":140594251},{"source":"dbSNP","start":140594252,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140594252,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1476388615"},{"start":140594256,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140594256,"alleles":["T","C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1004048217","clinical_significance":[]},{"clinical_significance":[],"id":"rs993116424","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594259,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140594259},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594261,"feature_type":"variation","strand":1,"end":140594261,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799190636"},{"seq_region_name":"7","id":"rs1799190751","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594267,"source":"dbSNP","strand":1,"feature_type":"variation","end":140594267,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs762048200","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594268,"feature_type":"variation","strand":1,"end":140594270,"alleles":["CCC","C"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594274,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140594274,"clinical_significance":[],"seq_region_name":"7","id":"rs1019947808"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594275,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140594275,"seq_region_name":"7","id":"rs1563165805","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799191294","clinical_significance":[],"start":140594275,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140594276,"alleles":["GT","-"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1585716793","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594278,"source":"dbSNP","strand":1,"feature_type":"variation","end":140594278,"alleles":["A","G"]},{"end":140594284,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140594284,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799191530","clinical_significance":[]},{"start":140594285,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140594285,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799191651","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1383526864","source":"dbSNP","start":140594286,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140594286,"alleles":["A","C"],"feature_type":"variation","strand":1},{"id":"rs779870509","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140594289,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594289,"source":"dbSNP"},{"alleles":["C","T"],"end":140594291,"strand":1,"feature_type":"variation","start":140594291,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799192052","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594293,"feature_type":"variation","strand":1,"end":140594293,"alleles":["C","T"],"clinical_significance":[],"id":"rs901125884","seq_region_name":"7"},{"end":140594295,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140594295,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799192342","seq_region_name":"7"},{"seq_region_name":"7","id":"rs374200553","clinical_significance":[],"strand":1,"feature_type":"variation","end":140594296,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594296,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799192660","clinical_significance":[],"strand":1,"feature_type":"variation","end":140594298,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594298,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1030077188","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594299,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140594299},{"clinical_significance":[],"id":"rs1799192901","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594303,"feature_type":"variation","strand":1,"end":140594303,"alleles":["A","G"]},{"alleles":["T","C"],"end":140594304,"strand":1,"feature_type":"variation","start":140594304,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799193012","clinical_significance":[]},{"clinical_significance":[],"id":"rs1585716855","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140594308,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594308},{"source":"dbSNP","start":140594309,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140594309,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799193288","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1311658347","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594313,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140594313},{"clinical_significance":[],"id":"rs1273875963","seq_region_name":"7","source":"dbSNP","start":140594317,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140594317,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594318,"source":"dbSNP","strand":1,"feature_type":"variation","end":140594318,"alleles":["C","T"],"seq_region_name":"7","id":"rs890208831","clinical_significance":[]},{"seq_region_name":"7","id":"rs76733497","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594322,"source":"dbSNP","strand":1,"feature_type":"variation","end":140594322,"alleles":["A","C"]},{"strand":1,"feature_type":"variation","end":140594323,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594323,"source":"dbSNP","seq_region_name":"7","id":"rs74759847","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799194025","clinical_significance":[],"start":140594329,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G","T"],"end":140594329,"strand":1,"feature_type":"variation"},{"alleles":["CCCC","CCC"],"end":140594333,"strand":1,"feature_type":"variation","start":140594330,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799194146","clinical_significance":[]},{"id":"rs1171401774","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140594331,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594331,"source":"dbSNP"},{"id":"rs1799194399","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140594332,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594332,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799194502","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594338,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140594338},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594342,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140594342,"seq_region_name":"7","id":"rs1799194644","clinical_significance":[]},{"alleles":["T","C"],"end":140594344,"strand":1,"feature_type":"variation","start":140594344,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1007231423","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799194905","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594346,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140594346},{"clinical_significance":[],"seq_region_name":"7","id":"rs1374523061","source":"dbSNP","start":140594347,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140594347,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130668927","source":"dbSNP","start":140594352,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140594352,"alleles":["A","G"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140594353,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594353,"source":"dbSNP","id":"rs1799195165","seq_region_name":"7","clinical_significance":[]},{"alleles":["GG","G"],"end":140594354,"strand":1,"feature_type":"variation","start":140594353,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1297534732","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140594354,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140594354,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1460295281"},{"seq_region_name":"7","id":"rs1453777039","clinical_significance":[],"strand":1,"feature_type":"variation","end":140594355,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594355,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs997072524","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594358,"feature_type":"variation","strand":1,"end":140594358,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1338263978","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140594360,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594360},{"clinical_significance":[],"id":"rs1799196162","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","A"],"end":140594364,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594364},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594365,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140594365,"clinical_significance":[],"seq_region_name":"7","id":"rs1017870166"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594366,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140594366,"clinical_significance":[],"seq_region_name":"7","id":"rs1406706557"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799196549","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594371,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140594371},{"clinical_significance":[],"seq_region_name":"7","id":"rs968768841","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594383,"feature_type":"variation","strand":1,"end":140594383,"alleles":["C","G","T"]},{"strand":1,"feature_type":"variation","end":140594384,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594384,"source":"dbSNP","seq_region_name":"7","id":"rs968559138","clinical_significance":[]},{"alleles":["T","C"],"end":140594385,"strand":1,"feature_type":"variation","start":140594385,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799196981","clinical_significance":[]},{"seq_region_name":"7","id":"rs1388193078","clinical_significance":[],"start":140594386,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140594386,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs979114205","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594388,"source":"dbSNP","strand":1,"feature_type":"variation","end":140594388,"alleles":["T","C","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799197360","end":140594389,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140594389,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1031578149","alleles":["A","C"],"end":140594391,"feature_type":"variation","strand":1,"source":"dbSNP","start":140594391,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140594394,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594394,"clinical_significance":[],"seq_region_name":"7","id":"rs1799197605"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1381414751","end":140594395,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140594395,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1799197860","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140594396,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594396,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140594399,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594399,"clinical_significance":[],"seq_region_name":"7","id":"rs571735385"},{"alleles":["T","A"],"end":140594402,"strand":1,"feature_type":"variation","start":140594402,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs956729061","clinical_significance":[]},{"end":140594406,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140594406,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs545377854"},{"end":140594409,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140594409,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs564055347","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs992880917","source":"dbSNP","start":140594416,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140594416,"alleles":["C","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799198676","source":"dbSNP","start":140594417,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140594417,"alleles":["C","G"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140594419,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140594433,"alleles":["ATTAGTTCACTCAAA","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1309593775"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130669122","alleles":["TTAGTT","TT"],"end":140594425,"feature_type":"variation","strand":1,"source":"dbSNP","start":140594420,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140594421,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594421,"clinical_significance":[],"seq_region_name":"7","id":"rs1340167995"},{"clinical_significance":[],"seq_region_name":"7","id":"rs917889419","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140594424,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594424},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594428,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140594428,"clinical_significance":[],"seq_region_name":"7","id":"rs2130669149"},{"seq_region_name":"7","id":"rs1799199245","clinical_significance":[],"strand":1,"feature_type":"variation","end":140594430,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594430,"source":"dbSNP"},{"id":"rs1799199375","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140594434,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594434,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1225658994","clinical_significance":[],"alleles":["T","C"],"end":140594435,"strand":1,"feature_type":"variation","start":140594435,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140594439,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","G","T"],"end":140594439,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs949460541","seq_region_name":"7"},{"seq_region_name":"7","id":"rs980855581","clinical_significance":[],"start":140594440,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140594440,"alleles":["G","A","C"],"strand":1,"feature_type":"variation"},{"end":140594443,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140594443,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs926807028","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594444,"feature_type":"variation","strand":1,"end":140594444,"alleles":["A","G"],"clinical_significance":[],"id":"rs1206192008","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140594445,"alleles":["C","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594445,"clinical_significance":[],"seq_region_name":"7","id":"rs949026449"},{"id":"rs1563165913","seq_region_name":"7","clinical_significance":[],"start":140594446,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140594446,"strand":1,"feature_type":"variation"},{"start":140594447,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140594447,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799200450","clinical_significance":[]},{"end":140594448,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140594448,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs942200313","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140594450,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594450,"clinical_significance":[],"id":"rs1038394286","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585717244","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140594451,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594451},{"end":140594452,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140594452,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1411086631","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140594454,"alleles":["CCC","CC"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594452,"source":"dbSNP","seq_region_name":"7","id":"rs1298414891","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140594454,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594454,"source":"dbSNP","id":"rs1799201237","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594456,"feature_type":"variation","strand":1,"end":140594456,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs898080522"},{"start":140594458,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","T"],"end":140594458,"strand":1,"feature_type":"variation","id":"rs550651038","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594458,"feature_type":"variation","strand":1,"end":140594461,"alleles":["CGCT","-"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799201665"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1425286595","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140594459,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594459},{"seq_region_name":"7","id":"rs1386857713","clinical_significance":[],"start":140594462,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["GGCCCGAG","G"],"end":140594469,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1799202081","clinical_significance":[],"end":140594463,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140594463,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594466,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140594466,"clinical_significance":[],"seq_region_name":"7","id":"rs777524537"},{"id":"rs929520928","seq_region_name":"7","clinical_significance":[],"end":140594467,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140594467,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs551335418","clinical_significance":[],"end":140594469,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140594469,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594470,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","G","T"],"end":140594470,"seq_region_name":"7","id":"rs748911081","clinical_significance":[]},{"alleles":["G","A"],"end":140594471,"strand":1,"feature_type":"variation","start":140594471,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1427013316","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1482100282","alleles":["C","A","T"],"end":140594473,"feature_type":"variation","strand":1,"source":"dbSNP","start":140594473,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1251246547","clinical_significance":[],"start":140594479,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140594479,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs2130669345","clinical_significance":[],"start":140594480,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140594480,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1223869954","source":"dbSNP","start":140594485,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140594485,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs890094345","source":"dbSNP","start":140594487,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140594487,"alleles":["C","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799203487","feature_type":"variation","strand":1,"end":140594490,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594490},{"seq_region_name":"7","id":"rs562690997","clinical_significance":[],"start":140594493,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140594493,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140594494,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594494,"source":"dbSNP","seq_region_name":"7","id":"rs1264216840","clinical_significance":[]},{"seq_region_name":"7","id":"rs886898692","clinical_significance":[],"alleles":["T","C"],"end":140594495,"strand":1,"feature_type":"variation","start":140594495,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1799203978","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594497,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140594497},{"seq_region_name":"7","id":"rs939676597","clinical_significance":[],"start":140594500,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140594500,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1799204102","seq_region_name":"7","source":"dbSNP","start":140594501,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140594501,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1040746021","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140594503,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594503},{"seq_region_name":"7","id":"rs1229903780","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594505,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140594505},{"alleles":["G","C"],"end":140594506,"strand":1,"feature_type":"variation","start":140594506,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1169471874","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1007741924","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594507,"feature_type":"variation","strand":1,"end":140594507,"alleles":["G","A","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs770411921","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594516,"feature_type":"variation","strand":1,"end":140594516,"alleles":["C","T"]},{"id":"rs1799204879","seq_region_name":"7","clinical_significance":[],"end":140594517,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140594517,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140594518,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594518,"source":"dbSNP","seq_region_name":"7","id":"rs904387022","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140594520,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594520,"clinical_significance":[],"seq_region_name":"7","id":"rs1405036499"},{"source":"dbSNP","start":140594531,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140594531,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799205133","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1291741976","feature_type":"variation","strand":1,"end":140594532,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594532},{"seq_region_name":"7","id":"rs1457186778","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594533,"source":"dbSNP","strand":1,"feature_type":"variation","end":140594533,"alleles":["A","G"]},{"feature_type":"variation","strand":1,"alleles":["G","C","T"],"end":140594536,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594536,"clinical_significance":[],"id":"rs1414898395","seq_region_name":"7"},{"end":140594539,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140594539,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585717552","clinical_significance":[]},{"end":140594543,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140594543,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799205768","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594545,"feature_type":"variation","strand":1,"end":140594545,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1161625625"},{"feature_type":"variation","strand":1,"end":140594548,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594548,"clinical_significance":[],"seq_region_name":"7","id":"rs1799206027"},{"id":"rs1799206151","seq_region_name":"7","clinical_significance":[],"start":140594550,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140594550,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1470877689","clinical_significance":[],"alleles":["CACAGCAC","CAC"],"end":140594557,"strand":1,"feature_type":"variation","start":140594550,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594552,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140594552,"clinical_significance":[],"seq_region_name":"7","id":"rs1174208455"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594555,"feature_type":"variation","strand":1,"end":140594555,"alleles":["C","T"],"clinical_significance":[],"id":"rs1000029420","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs901069370","source":"dbSNP","start":140594557,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140594557,"feature_type":"variation","strand":1},{"alleles":["C","G"],"end":140594561,"feature_type":"variation","strand":1,"source":"dbSNP","start":140594561,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1481447807","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1265930690","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140594565,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594565,"source":"dbSNP"},{"end":140594566,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140594566,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs531473370","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140594570,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594570,"clinical_significance":[],"seq_region_name":"7","id":"rs549569186"},{"seq_region_name":"7","id":"rs1799207346","clinical_significance":[],"alleles":["C","A"],"end":140594574,"strand":1,"feature_type":"variation","start":140594574,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs955946556","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594576,"source":"dbSNP","strand":1,"feature_type":"variation","end":140594576,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1486410419","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594577,"feature_type":"variation","strand":1,"end":140594577,"alleles":["G","A","C"]},{"start":140594583,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140594583,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799207755","clinical_significance":[]},{"seq_region_name":"7","id":"rs992714370","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140594589,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594589,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799207995","clinical_significance":[],"alleles":["T","C"],"end":140594590,"strand":1,"feature_type":"variation","start":140594590,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1585717688","seq_region_name":"7","clinical_significance":[],"alleles":["C","A","T"],"end":140594599,"strand":1,"feature_type":"variation","start":140594599,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1585717700","seq_region_name":"7","clinical_significance":[],"end":140594600,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140594600,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1262804517","source":"dbSNP","start":140594601,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140594601,"alleles":["A","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1028128496","clinical_significance":[],"strand":1,"feature_type":"variation","end":140594602,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594602,"source":"dbSNP"},{"id":"rs74566475","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140594604,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594604,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1287307347","clinical_significance":[],"start":140594608,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140594608,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140594612,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140594612,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs970698396"},{"seq_region_name":"7","id":"rs2130669623","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140594615,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594615,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140594617,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594617,"source":"dbSNP","seq_region_name":"7","id":"rs1799209048","clinical_significance":[]},{"source":"dbSNP","start":140594620,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140594620,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1290160692"},{"clinical_significance":[],"seq_region_name":"7","id":"rs562676200","end":140594621,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140594621,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799209462","end":140594628,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140594628,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140594629,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140594632,"alleles":["AGAG","AG"],"strand":1,"feature_type":"variation","id":"rs1799209591","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs190053649","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594630,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140594630},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799209857","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594631,"feature_type":"variation","strand":1,"end":140594631,"alleles":["A","G"]},{"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140594633,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594633,"clinical_significance":[],"seq_region_name":"7","id":"rs1799209981"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1299139717","end":140594636,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140594636,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140594637,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594637,"source":"dbSNP","seq_region_name":"7","id":"rs370913806","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140594638,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594638,"source":"dbSNP","id":"rs926721661","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1362410151","seq_region_name":"7","source":"dbSNP","start":140594638,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140594638,"alleles":["G","-"],"feature_type":"variation","strand":1},{"start":140594640,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140594640,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs143759742","clinical_significance":[]},{"seq_region_name":"7","id":"rs1177381221","clinical_significance":[],"start":140594643,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140594643,"strand":1,"feature_type":"variation"},{"end":140594646,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140594646,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs539878968"},{"alleles":["G","A"],"end":140594647,"feature_type":"variation","strand":1,"source":"dbSNP","start":140594647,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs919394502"},{"clinical_significance":[],"seq_region_name":"7","id":"rs551769333","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594648,"feature_type":"variation","strand":1,"end":140594648,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1799211196","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594650,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140594650},{"clinical_significance":[],"id":"rs920724407","seq_region_name":"7","end":140594659,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140594659,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1187127965","feature_type":"variation","strand":1,"end":140594662,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594662},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140594666,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594666,"source":"dbSNP","id":"rs138496109","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1216546849","clinical_significance":[],"alleles":["C","T"],"end":140594677,"strand":1,"feature_type":"variation","start":140594677,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140594678,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594678,"source":"dbSNP","seq_region_name":"7","id":"rs929576430","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140594680,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594680,"source":"dbSNP","id":"rs775807144","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799211994","alleles":["G","A"],"end":140594683,"feature_type":"variation","strand":1,"source":"dbSNP","start":140594683,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","A","T"],"end":140594686,"feature_type":"variation","strand":1,"source":"dbSNP","start":140594686,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799212107","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594687,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140594687,"seq_region_name":"7","id":"rs74558397","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140594696,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594696,"source":"dbSNP","seq_region_name":"7","id":"rs1799212384","clinical_significance":[]},{"start":140594700,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140594700,"alleles":["G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799212488","clinical_significance":[]},{"id":"rs2130669851","seq_region_name":"7","clinical_significance":[],"start":140594701,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140594701,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140594703,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594703,"source":"dbSNP","id":"rs1231889757","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799212674","feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140594704,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594704},{"seq_region_name":"7","id":"rs983619337","clinical_significance":[],"end":140594713,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140594713,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs911583422","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594718,"source":"dbSNP","strand":1,"feature_type":"variation","end":140594718,"alleles":["T","A","C"]},{"strand":1,"feature_type":"variation","alleles":["TGAGT","T"],"end":140594722,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594718,"source":"dbSNP","seq_region_name":"7","id":"rs1299709347","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594719,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140594719,"clinical_significance":[],"id":"rs555774057","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1039233718","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594721,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140594721},{"seq_region_name":"7","id":"rs1799213467","clinical_significance":[],"strand":1,"feature_type":"variation","end":140594728,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594728,"source":"dbSNP"},{"alleles":["T","C"],"end":140594730,"strand":1,"feature_type":"variation","start":140594730,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799213590","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140594747,"alleles":["TTATTTATTTATTT","TTATTTATTT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594734,"clinical_significance":[],"seq_region_name":"7","id":"rs1799213700"},{"id":"rs1799213823","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140594738,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594738,"source":"dbSNP"},{"start":140594741,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140594741,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799213927","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799214039","seq_region_name":"7","alleles":["A","G"],"end":140594744,"feature_type":"variation","strand":1,"source":"dbSNP","start":140594744,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585718046","alleles":["T","G"],"end":140594748,"feature_type":"variation","strand":1,"source":"dbSNP","start":140594748,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140594749,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140594749,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs181894746","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594750,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C","T"],"end":140594750,"seq_region_name":"7","id":"rs761068397","clinical_significance":[]},{"alleles":["C","T"],"end":140594751,"strand":1,"feature_type":"variation","start":140594751,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1269266937","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","G","T"],"end":140594753,"feature_type":"variation","strand":1,"source":"dbSNP","start":140594753,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1172131811"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1462548776","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594755,"feature_type":"variation","strand":1,"end":140594755,"alleles":["G","A","C"]},{"source":"dbSNP","start":140594757,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140594757,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1052953319"},{"clinical_significance":[],"seq_region_name":"7","id":"rs370891839","source":"dbSNP","start":140594758,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140594758,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs764472527","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140594761,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594761,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140594763,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594763,"clinical_significance":[],"seq_region_name":"7","id":"rs1799215400"},{"clinical_significance":[],"seq_region_name":"7","id":"rs750453283","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594766,"feature_type":"variation","strand":1,"end":140594767,"alleles":["GG","GGG"]},{"source":"dbSNP","start":140594767,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140594767,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799215606"},{"source":"dbSNP","start":140594774,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G","T"],"end":140594774,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1024214257"},{"alleles":["G","A"],"end":140594776,"strand":1,"feature_type":"variation","start":140594776,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1563166143","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140594778,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594778,"source":"dbSNP","seq_region_name":"7","id":"rs1187826994","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585718175","feature_type":"variation","strand":1,"end":140594779,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594779},{"alleles":["A","G"],"end":140594781,"strand":1,"feature_type":"variation","start":140594781,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799216180","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799216296","clinical_significance":[],"strand":1,"feature_type":"variation","end":140594783,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594783,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs932524968","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594788,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140594788},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594790,"feature_type":"variation","strand":1,"end":140594790,"alleles":["C","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1443856369"},{"seq_region_name":"7","id":"rs2130670095","clinical_significance":[],"start":140594795,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140594795,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140594797,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594797,"source":"dbSNP","id":"rs1563166151","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1390098030","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594802,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140594802},{"start":140594809,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140594809,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799216770","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs776865065","feature_type":"variation","strand":1,"end":140594810,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594810},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594813,"feature_type":"variation","strand":1,"end":140594813,"alleles":["T","C","G"],"clinical_significance":[],"id":"rs1799217008","seq_region_name":"7"},{"alleles":["A","G","T"],"end":140594816,"feature_type":"variation","strand":1,"source":"dbSNP","start":140594816,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1160633617"},{"end":140594817,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140594817,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1276729487","clinical_significance":[]},{"end":140594818,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140594818,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs549229520"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799217412","alleles":["G","A"],"end":140594819,"feature_type":"variation","strand":1,"source":"dbSNP","start":140594819,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1341212919","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594826,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140594826},{"strand":1,"feature_type":"variation","end":140594828,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594828,"source":"dbSNP","seq_region_name":"7","id":"rs1799217628","clinical_significance":[]},{"seq_region_name":"7","id":"rs1315397055","clinical_significance":[],"alleles":["C","T"],"end":140594830,"strand":1,"feature_type":"variation","start":140594830,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799218572","feature_type":"variation","strand":1,"end":140594833,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594833},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594836,"source":"dbSNP","strand":1,"feature_type":"variation","end":140594836,"alleles":["C","T"],"id":"rs904478895","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs372746476","seq_region_name":"7","source":"dbSNP","start":140594841,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140594841,"alleles":["A","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1799218898","seq_region_name":"7","feature_type":"variation","strand":1,"end":140594844,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594844},{"seq_region_name":"7","id":"rs1799218990","clinical_significance":[],"alleles":["G","A"],"end":140594849,"strand":1,"feature_type":"variation","start":140594849,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140594852,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140594852,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799219090"},{"end":140594856,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140594856,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1333726022","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140594857,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594857,"source":"dbSNP","seq_region_name":"7","id":"rs1799219278","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130670236","clinical_significance":[],"strand":1,"feature_type":"variation","end":140594859,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594859,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1392074134","source":"dbSNP","start":140594861,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140594861,"feature_type":"variation","strand":1},{"end":140594862,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140594862,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs571772382"},{"start":140594863,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140594863,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1306738119","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594864,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140594864,"seq_region_name":"7","id":"rs1429602691","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799220005","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594866,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140594866},{"clinical_significance":[],"id":"rs1799220159","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594867,"feature_type":"variation","strand":1,"end":140594867,"alleles":["C","A"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594874,"feature_type":"variation","strand":1,"end":140594874,"alleles":["C","T"],"clinical_significance":[],"id":"rs750536863","seq_region_name":"7"},{"alleles":["G","T"],"end":140594878,"strand":1,"feature_type":"variation","start":140594878,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1165423863","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585718356","end":140594883,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140594883,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140594889,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594889,"source":"dbSNP","seq_region_name":"7","id":"rs973869391","clinical_significance":[]},{"source":"dbSNP","start":140594890,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140594890,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1366397169"},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140594891,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594891,"source":"dbSNP","seq_region_name":"7","id":"rs1799221144","clinical_significance":[]},{"end":140594896,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140594896,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799221255","clinical_significance":[]},{"alleles":["T","G"],"end":140594898,"strand":1,"feature_type":"variation","start":140594898,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585718380","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594900,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140594900,"clinical_significance":[],"seq_region_name":"7","id":"rs1686483439"},{"id":"rs919446770","seq_region_name":"7","clinical_significance":[],"start":140594902,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140594902,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140594904,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594904,"clinical_significance":[],"seq_region_name":"7","id":"rs1346490136"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1253274413","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140594906,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594906},{"start":140594908,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140594908,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799221618","clinical_significance":[]},{"clinical_significance":[],"id":"rs1202941760","seq_region_name":"7","source":"dbSNP","start":140594917,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140594917,"feature_type":"variation","strand":1},{"start":140594918,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140594918,"alleles":["G","C"],"strand":1,"feature_type":"variation","id":"rs950868357","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140594925,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140594925,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1482725860","seq_region_name":"7"},{"id":"rs1799221994","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594926,"source":"dbSNP","strand":1,"feature_type":"variation","end":140594926,"alleles":["G","A"]},{"alleles":["G","T"],"end":140594927,"feature_type":"variation","strand":1,"source":"dbSNP","start":140594927,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1292391167","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594931,"feature_type":"variation","strand":1,"end":140594931,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799222214"},{"start":140594935,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140594935,"strand":1,"feature_type":"variation","id":"rs1052968236","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs754956835","seq_region_name":"7","alleles":["G","A"],"end":140594936,"feature_type":"variation","strand":1,"source":"dbSNP","start":140594936,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1799222582","clinical_significance":[],"alleles":["C","T"],"end":140594939,"strand":1,"feature_type":"variation","start":140594939,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140594943,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140594943,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1283851467","seq_region_name":"7"},{"seq_region_name":"7","id":"rs891855894","clinical_significance":[],"start":140594948,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TT","TTT"],"end":140594949,"strand":1,"feature_type":"variation"},{"start":140594952,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140594952,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799222929","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799223026","source":"dbSNP","start":140594953,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140594953,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1014359937","source":"dbSNP","start":140594954,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140594954,"alleles":["T","A","C"],"feature_type":"variation","strand":1},{"start":140594956,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140594956,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs767615324","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs943577621","source":"dbSNP","start":140594957,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140594957,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1366791454","source":"dbSNP","start":140594960,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140594960,"alleles":["T","G"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140594967,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594967,"source":"dbSNP","seq_region_name":"7","id":"rs1799223630","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1038702095","source":"dbSNP","start":140594970,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140594970,"alleles":["T","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1326075819","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594982,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140594982},{"start":140594983,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140594983,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs2130670479","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs752513344","end":140594989,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140594989,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1390407645","clinical_significance":[],"start":140594993,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140594993,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140594994,"alleles":["G","A","C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140594994,"clinical_significance":[],"seq_region_name":"7","id":"rs1309150922"},{"alleles":["T","A"],"end":140594995,"strand":1,"feature_type":"variation","start":140594995,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1472676024","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594996,"source":"dbSNP","strand":1,"feature_type":"variation","end":140594996,"alleles":["G","A"],"seq_region_name":"7","id":"rs1799224514","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140594998,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140594998,"source":"dbSNP","seq_region_name":"7","id":"rs545416029","clinical_significance":[]},{"seq_region_name":"7","id":"rs1215275799","clinical_significance":[],"start":140594999,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140594999,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140595000,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140595000,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs567566015","seq_region_name":"7"},{"end":140595003,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140595003,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1179460308","clinical_significance":[]},{"id":"rs1799225091","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140595004,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595004,"source":"dbSNP"},{"seq_region_name":"7","id":"rs935782678","clinical_significance":[],"strand":1,"feature_type":"variation","end":140595006,"alleles":["G","C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595006,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595008,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140595008,"clinical_significance":[],"id":"rs2130670574","seq_region_name":"7"},{"end":140595026,"alleles":["TTTTGTTTTTTG","TTTTG"],"strand":1,"feature_type":"variation","start":140595015,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1027855414","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595019,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140595019,"clinical_significance":[],"seq_region_name":"7","id":"rs952328304"},{"seq_region_name":"7","id":"rs983566890","clinical_significance":[],"alleles":["T","G"],"end":140595020,"strand":1,"feature_type":"variation","start":140595020,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1799225700","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595024,"source":"dbSNP","strand":1,"feature_type":"variation","end":140595024,"alleles":["T","C"]},{"source":"dbSNP","start":140595025,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140595025,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1052836893"},{"start":140595031,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140595031,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs1209120876","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1292823276","source":"dbSNP","start":140595032,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140595032,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595035,"feature_type":"variation","strand":1,"end":140595035,"alleles":["T","C"],"clinical_significance":[],"id":"rs891662390","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595035,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","-"],"end":140595035,"id":"rs1799226315","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799226429","clinical_significance":[],"end":140595043,"alleles":["TCTTGCTCT","TCT"],"strand":1,"feature_type":"variation","start":140595035,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["TTGCT","-"],"end":140595041,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595037,"clinical_significance":[],"seq_region_name":"7","id":"rs1799226540"},{"source":"dbSNP","start":140595038,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140595038,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799226649"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799226764","alleles":["C","G"],"end":140595040,"feature_type":"variation","strand":1,"source":"dbSNP","start":140595040,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140595041,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595041,"source":"dbSNP","seq_region_name":"7","id":"rs908071640","clinical_significance":[]},{"alleles":["C","A"],"end":140595048,"strand":1,"feature_type":"variation","start":140595048,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799226870","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140595051,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595051,"clinical_significance":[],"id":"rs1227910219","seq_region_name":"7"},{"alleles":["C","G"],"end":140595053,"strand":1,"feature_type":"variation","start":140595053,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1346187768","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140595059,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595059,"clinical_significance":[],"seq_region_name":"7","id":"rs1277144061"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1434866817","feature_type":"variation","strand":1,"alleles":["C","-"],"end":140595061,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595061},{"id":"rs1490914265","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595061,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140595061},{"id":"rs1319468423","seq_region_name":"7","clinical_significance":[],"start":140595062,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140595062,"strand":1,"feature_type":"variation"},{"start":140595063,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140595063,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1459145042","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595064,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140595064,"seq_region_name":"7","id":"rs1358782967","clinical_significance":[]},{"alleles":["A","G"],"end":140595071,"strand":1,"feature_type":"variation","start":140595071,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1585718780","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1390442378","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595072,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140595072},{"alleles":["C","T"],"end":140595075,"strand":1,"feature_type":"variation","start":140595075,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs377375062","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595076,"source":"dbSNP","strand":1,"feature_type":"variation","end":140595076,"alleles":["G","A"],"seq_region_name":"7","id":"rs1267984061","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585718832","clinical_significance":[],"start":140595087,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140595087,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140595088,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595088,"clinical_significance":[],"seq_region_name":"7","id":"rs187346229"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1456275180","source":"dbSNP","start":140595089,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140595089,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140595092,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595092,"clinical_significance":[],"seq_region_name":"7","id":"rs1470467607"},{"id":"rs1585718864","seq_region_name":"7","clinical_significance":[],"start":140595093,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140595093,"alleles":["A","C","G"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140595095,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140595095,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1178879188"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595101,"source":"dbSNP","strand":1,"feature_type":"variation","end":140595101,"alleles":["G","A","T"],"id":"rs771072489","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595107,"source":"dbSNP","strand":1,"feature_type":"variation","end":140595107,"alleles":["T","C"],"id":"rs1405086123","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1045719078","clinical_significance":[],"strand":1,"feature_type":"variation","end":140595108,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595108,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140595111,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595111,"clinical_significance":[],"id":"rs1799229344","seq_region_name":"7"},{"end":140595113,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140595113,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799229452","clinical_significance":[]},{"start":140595114,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140595114,"strand":1,"feature_type":"variation","id":"rs1476960270","seq_region_name":"7","clinical_significance":[]},{"end":140595116,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140595116,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs537880939"},{"end":140595118,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140595118,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs922219730","seq_region_name":"7"},{"seq_region_name":"7","id":"rs561834011","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595120,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140595120},{"clinical_significance":[],"seq_region_name":"7","id":"rs1246459205","alleles":["C","T"],"end":140595121,"feature_type":"variation","strand":1,"source":"dbSNP","start":140595121,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595129,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140595129,"clinical_significance":[],"seq_region_name":"7","id":"rs1585718948"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1367015421","source":"dbSNP","start":140595131,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140595131,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1033700216","clinical_significance":[],"strand":1,"feature_type":"variation","end":140595132,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595132,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140595137,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595137,"source":"dbSNP","seq_region_name":"7","id":"rs1799230571","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140595146,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595146,"source":"dbSNP","seq_region_name":"7","id":"rs1301674374","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140595148,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595148,"source":"dbSNP","seq_region_name":"7","id":"rs192071101","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140595149,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595149,"clinical_significance":[],"seq_region_name":"7","id":"rs1443490008"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595150,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140595150,"clinical_significance":[],"seq_region_name":"7","id":"rs1217542579"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1344993705","source":"dbSNP","start":140595151,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140595151,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1298960131","feature_type":"variation","strand":1,"end":140595153,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595153},{"strand":1,"feature_type":"variation","end":140595156,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595156,"source":"dbSNP","seq_region_name":"7","id":"rs1799231403","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140595159,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595159,"source":"dbSNP","seq_region_name":"7","id":"rs1437774594","clinical_significance":[]},{"start":140595160,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140595160,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1363416549","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799231735","source":"dbSNP","start":140595163,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140595163,"alleles":["T","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1799231871","clinical_significance":[],"strand":1,"feature_type":"variation","end":140595165,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595165,"source":"dbSNP"},{"end":140595169,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140595169,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1318149877","clinical_significance":[]},{"alleles":["T","C"],"end":140595171,"strand":1,"feature_type":"variation","start":140595171,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs180812650","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799232262","feature_type":"variation","strand":1,"end":140595173,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595173},{"start":140595174,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140595174,"strand":1,"feature_type":"variation","id":"rs1799232462","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1026345761","clinical_significance":[],"strand":1,"feature_type":"variation","end":140595182,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595182,"source":"dbSNP"},{"end":140595186,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140595186,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs925846501","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799233070","clinical_significance":[],"strand":1,"feature_type":"variation","end":140595189,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595189,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595190,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140595190,"id":"rs935926533","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595194,"source":"dbSNP","strand":1,"feature_type":"variation","end":140595194,"alleles":["A","C"],"seq_region_name":"7","id":"rs1371229231","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1424428113","feature_type":"variation","strand":1,"end":140595196,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595196},{"strand":1,"feature_type":"variation","end":140595199,"alleles":["AGAG","AG"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595196,"source":"dbSNP","id":"rs1799233954","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140595197,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595197,"clinical_significance":[],"seq_region_name":"7","id":"rs1799234104"},{"clinical_significance":[],"id":"rs1052917183","seq_region_name":"7","end":140595201,"alleles":["AGTT","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140595198,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140595206,"alleles":["CCCC","CCC"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595203,"clinical_significance":[],"seq_region_name":"7","id":"rs1451124879"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130671051","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140595207,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595207},{"seq_region_name":"7","id":"rs1245905107","clinical_significance":[],"start":140595209,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140595209,"strand":1,"feature_type":"variation"},{"start":140595210,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140595210,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1315885596","clinical_significance":[]},{"end":140595212,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140595212,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs755936805","clinical_significance":[]},{"start":140595214,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140595214,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1361840939","clinical_significance":[]},{"end":140595217,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140595217,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs144076114","clinical_significance":[]},{"id":"rs1288795086","seq_region_name":"7","clinical_significance":[],"alleles":["T","A","G"],"end":140595223,"strand":1,"feature_type":"variation","start":140595223,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs556113749","seq_region_name":"7","clinical_significance":[],"start":140595224,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140595224,"strand":1,"feature_type":"variation"},{"id":"rs112764628","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140595232,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595232,"source":"dbSNP"},{"source":"dbSNP","start":140595234,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140595234,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs571452976"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1231191302","source":"dbSNP","start":140595237,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140595237,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595240,"feature_type":"variation","strand":1,"alleles":["CAAGTGATCTGCCCACC","CAAGTGATCTGCCCACCAAGTGATCTGCCCACC"],"end":140595256,"clinical_significance":[],"id":"rs1799235733","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1340495553","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595241,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140595241},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595243,"feature_type":"variation","strand":1,"end":140595243,"alleles":["G","A"],"clinical_significance":[],"id":"rs185204096","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140595253,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595253,"source":"dbSNP","id":"rs2130671166","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585719241","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140595254,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595254,"source":"dbSNP"},{"source":"dbSNP","start":140595255,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140595255,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1480290519","seq_region_name":"7"},{"alleles":["T","C"],"end":140595257,"feature_type":"variation","strand":1,"source":"dbSNP","start":140595257,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs113256092"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799236497","source":"dbSNP","start":140595258,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140595258,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799236592","feature_type":"variation","strand":1,"end":140595259,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595259},{"clinical_significance":[],"id":"rs1379511287","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595261,"feature_type":"variation","strand":1,"end":140595261,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1183644125","clinical_significance":[],"start":140595262,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140595262,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"start":140595267,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140595267,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1386629396","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140595275,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595275,"clinical_significance":[],"id":"rs1358026385","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140595277,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595277,"source":"dbSNP","seq_region_name":"7","id":"rs1308576474","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595284,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140595284,"clinical_significance":[],"id":"rs905976949","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1585719351","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140595286,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595286},{"clinical_significance":[],"id":"rs1388245263","seq_region_name":"7","source":"dbSNP","start":140595287,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140595287,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585719367","source":"dbSNP","start":140595295,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140595295,"alleles":["C","A"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595300,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140595300,"clinical_significance":[],"id":"rs1799237758","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs965001189","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140595303,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595303},{"clinical_significance":[],"seq_region_name":"7","id":"rs189915073","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140595304,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595304},{"id":"rs1799238121","seq_region_name":"7","clinical_significance":[],"start":140595306,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","T"],"end":140595306,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140595308,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595308,"source":"dbSNP","seq_region_name":"7","id":"rs925665443","clinical_significance":[]},{"start":140595309,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140595309,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1027636828","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563166482","feature_type":"variation","strand":1,"alleles":["TGAATGAAT","TGAAT"],"end":140595318,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595310},{"seq_region_name":"7","id":"rs1799238609","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595313,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140595313},{"start":140595315,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140595315,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs1413463854","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130671357","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140595329,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595329},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799238857","feature_type":"variation","strand":1,"end":140595332,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595332},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595338,"feature_type":"variation","strand":1,"end":140595338,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1472520454"},{"seq_region_name":"7","id":"rs1252553948","clinical_significance":[],"strand":1,"feature_type":"variation","end":140595341,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595341,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1207920989","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140595344,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595344,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595349,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140595349,"seq_region_name":"7","id":"rs1482397159","clinical_significance":[]},{"start":140595351,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140595351,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799239325","clinical_significance":[]},{"alleles":["T","A"],"end":140595352,"feature_type":"variation","strand":1,"source":"dbSNP","start":140595352,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs935651967"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1323841066","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595366,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140595366},{"clinical_significance":[],"seq_region_name":"7","id":"rs1222829284","end":140595368,"alleles":["CCC","CC"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140595366,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1314462632","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595368,"feature_type":"variation","strand":1,"end":140595368,"alleles":["C","A","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs146894149","feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140595369,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595369},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799240138","end":140595371,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140595371,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1015474787","seq_region_name":"7","feature_type":"variation","strand":1,"end":140595374,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595374},{"strand":1,"feature_type":"variation","end":140595376,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595376,"source":"dbSNP","seq_region_name":"7","id":"rs1799240426","clinical_significance":[]},{"source":"dbSNP","start":140595377,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140595377,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1353249427"},{"id":"rs1799240636","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595378,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140595378},{"end":140595379,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140595379,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1446773843","clinical_significance":[]},{"id":"rs912983900","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595381,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140595381},{"start":140595382,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140595382,"strand":1,"feature_type":"variation","id":"rs949745820","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs879782639","clinical_significance":[],"end":140595392,"alleles":["AAAAAAAAAAA","AAAAAAAAAA","AAAAAAAAAAAA"],"strand":1,"feature_type":"variation","start":140595382,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["A","G"],"end":140595385,"strand":1,"feature_type":"variation","start":140595385,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1045598385","clinical_significance":[]},{"clinical_significance":[],"id":"rs2130671523","seq_region_name":"7","feature_type":"variation","strand":1,"end":140595390,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595390},{"start":140595392,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140595392,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799241364","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140595394,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595394,"source":"dbSNP","seq_region_name":"7","id":"rs1799241479","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140595396,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595396,"clinical_significance":[],"seq_region_name":"7","id":"rs756923464"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595397,"feature_type":"variation","strand":1,"end":140595397,"alleles":["C","A"],"clinical_significance":[],"id":"rs1450643349","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140595399,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595399,"source":"dbSNP","seq_region_name":"7","id":"rs1799241830","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1283840019","source":"dbSNP","start":140595401,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140595401,"alleles":["A","G","T"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140595402,"alleles":["T","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595402,"source":"dbSNP","id":"rs1339783095","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799242239","feature_type":"variation","strand":1,"alleles":["T","A"],"end":140595403,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595403},{"source":"dbSNP","start":140595405,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140595405,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs530923610","seq_region_name":"7"},{"end":140595411,"alleles":["TTGAGTT","TT"],"strand":1,"feature_type":"variation","start":140595405,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1423393865","clinical_significance":[]},{"clinical_significance":[],"id":"rs1184507077","seq_region_name":"7","alleles":["G","C"],"end":140595407,"feature_type":"variation","strand":1,"source":"dbSNP","start":140595407,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1216075410","alleles":["G","A"],"end":140595409,"feature_type":"variation","strand":1,"source":"dbSNP","start":140595409,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140595410,"alleles":["T","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595410,"source":"dbSNP","seq_region_name":"7","id":"rs139369295","clinical_significance":[]},{"start":140595414,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140595414,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs567847069","clinical_significance":[]},{"seq_region_name":"7","id":"rs1489681152","clinical_significance":[],"start":140595418,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140595418,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140595420,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595420,"source":"dbSNP","seq_region_name":"7","id":"rs1317209215","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799243356","seq_region_name":"7","feature_type":"variation","strand":1,"end":140595427,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595427},{"start":140595433,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140595433,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799243456","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140595435,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595435,"clinical_significance":[],"seq_region_name":"7","id":"rs1799243580"},{"seq_region_name":"7","id":"rs1221292796","clinical_significance":[],"start":140595436,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140595436,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799243811","feature_type":"variation","strand":1,"end":140595437,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595437},{"clinical_significance":[],"id":"rs1563166572","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["CCCCC","CCCC"],"end":140595446,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595442},{"source":"dbSNP","start":140595448,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140595448,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799244033"},{"source":"dbSNP","start":140595458,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140595458,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799244141","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130671688","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595459,"feature_type":"variation","strand":1,"end":140595459,"alleles":["C","A"]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140595462,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595462,"clinical_significance":[],"seq_region_name":"7","id":"rs1799244248"},{"id":"rs551695947","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595463,"source":"dbSNP","strand":1,"feature_type":"variation","end":140595463,"alleles":["A","G"]},{"source":"dbSNP","start":140595464,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140595464,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1268346066"},{"seq_region_name":"7","id":"rs1799244625","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595466,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140595466},{"strand":1,"feature_type":"variation","alleles":["AAAAAA","AAAAA","AAAAAAA"],"end":140595475,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595470,"source":"dbSNP","seq_region_name":"7","id":"rs1229740431","clinical_significance":[]},{"clinical_significance":[],"id":"rs10242147","seq_region_name":"7","source":"dbSNP","start":140595476,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140595476,"alleles":["G","C","T"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140595478,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595478,"source":"dbSNP","seq_region_name":"7","id":"rs553262720","clinical_significance":[]},{"alleles":["A","G"],"end":140595486,"strand":1,"feature_type":"variation","start":140595486,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799245320","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595488,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140595488,"clinical_significance":[],"seq_region_name":"7","id":"rs1186351604"},{"end":140595492,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140595492,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1799245687","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140595493,"alleles":["G","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595493,"clinical_significance":[],"seq_region_name":"7","id":"rs994791207"},{"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140595494,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595494,"source":"dbSNP","seq_region_name":"7","id":"rs1585719779","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140595496,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595496,"source":"dbSNP","seq_region_name":"7","id":"rs565440342","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585719797","clinical_significance":[],"start":140595501,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140595501,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"end":140595502,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140595502,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585719808"},{"end":140595505,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140595505,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1585719817","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140595506,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595506,"clinical_significance":[],"seq_region_name":"7","id":"rs1026232042"},{"clinical_significance":[],"seq_region_name":"7","id":"rs886532088","feature_type":"variation","strand":1,"end":140595507,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595507},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595508,"source":"dbSNP","strand":1,"feature_type":"variation","end":140595508,"alleles":["C","T"],"seq_region_name":"7","id":"rs1799247215","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585719856","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595510,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140595510},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595511,"feature_type":"variation","strand":1,"end":140595511,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs935873571"},{"strand":1,"feature_type":"variation","end":140595512,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595512,"source":"dbSNP","seq_region_name":"7","id":"rs1799247576","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595518,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140595518,"clinical_significance":[],"seq_region_name":"7","id":"rs1799247684"},{"id":"rs1799247786","seq_region_name":"7","clinical_significance":[],"alleles":["A","G"],"end":140595519,"strand":1,"feature_type":"variation","start":140595519,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1799247917","clinical_significance":[],"end":140595520,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140595520,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1799248052","clinical_significance":[],"end":140595521,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140595521,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs111458013","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595526,"source":"dbSNP","strand":1,"feature_type":"variation","end":140595526,"alleles":["T","A","C"]},{"alleles":["G","A"],"end":140595531,"feature_type":"variation","strand":1,"source":"dbSNP","start":140595531,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1465500010"},{"start":140595534,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140595534,"strand":1,"feature_type":"variation","id":"rs913180306","seq_region_name":"7","clinical_significance":[]},{"end":140595538,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140595538,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1191031553"},{"seq_region_name":"7","id":"rs1019127596","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595540,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140595540},{"seq_region_name":"7","id":"rs1465604250","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140595546,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595546,"source":"dbSNP"},{"end":140595548,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140595548,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1177799143"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1326475490","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595549,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140595549},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595550,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140595550,"id":"rs1799249213","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130671936","feature_type":"variation","strand":1,"end":140595566,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595566},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799249311","source":"dbSNP","start":140595568,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140595568,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140595570,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140595570,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1585719947","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799249555","source":"dbSNP","start":140595574,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140595574,"alleles":["G","T"],"feature_type":"variation","strand":1},{"id":"rs1799249674","seq_region_name":"7","clinical_significance":[],"start":140595575,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140595575,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs965223466","clinical_significance":[],"end":140595578,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140595578,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1259559064","alleles":["G","A"],"end":140595579,"feature_type":"variation","strand":1,"source":"dbSNP","start":140595579,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1233328830","clinical_significance":[],"start":140595580,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140595580,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1313937326","clinical_significance":[],"strand":1,"feature_type":"variation","end":140595585,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595585,"source":"dbSNP"},{"id":"rs949907357","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140595586,"alleles":["T","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595586,"source":"dbSNP"},{"id":"rs1439939149","seq_region_name":"7","clinical_significance":[],"start":140595587,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140595587,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1799250534","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140595589,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595589},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585720004","source":"dbSNP","start":140595593,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140595593,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1046006734","end":140595594,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140595594,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595596,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140595596,"clinical_significance":[],"seq_region_name":"7","id":"rs182533274"},{"alleles":["C","T"],"end":140595605,"strand":1,"feature_type":"variation","start":140595605,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs554079550","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595606,"source":"dbSNP","strand":1,"feature_type":"variation","end":140595606,"alleles":["A","T"],"seq_region_name":"7","id":"rs1433088604","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799251270","clinical_significance":[],"start":140595606,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AAAAAA","AAAAAAA"],"end":140595611,"strand":1,"feature_type":"variation"},{"id":"rs1384522053","seq_region_name":"7","clinical_significance":[],"start":140595614,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140595614,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"end":140595627,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140595627,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1173292863","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs543030943","source":"dbSNP","start":140595628,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140595628,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140595629,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595629,"clinical_significance":[],"seq_region_name":"7","id":"rs1467629936"},{"clinical_significance":[],"id":"rs1585720104","seq_region_name":"7","source":"dbSNP","start":140595630,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140595630,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs937446584","source":"dbSNP","start":140595631,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140595631,"feature_type":"variation","strand":1},{"start":140595635,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140595635,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1033671005","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799252173","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595636,"source":"dbSNP","strand":1,"feature_type":"variation","end":140595636,"alleles":["G","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1333638406","feature_type":"variation","strand":1,"end":140595637,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595637},{"source":"dbSNP","start":140595638,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140595638,"alleles":["A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799252394"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799252504","source":"dbSNP","start":140595639,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140595639,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140595640,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140595640,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799252612"},{"alleles":["T","C"],"end":140595641,"feature_type":"variation","strand":1,"source":"dbSNP","start":140595641,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799252721"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1450501945","source":"dbSNP","start":140595642,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140595642,"alleles":["G","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1799252942","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595643,"source":"dbSNP","strand":1,"feature_type":"variation","end":140595643,"alleles":["C","T"]},{"alleles":["T","C","G"],"end":140595645,"strand":1,"feature_type":"variation","start":140595645,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs187192808","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799253227","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595648,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140595648},{"clinical_significance":[],"seq_region_name":"7","id":"rs1463316460","end":140595650,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140595650,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs772535470","seq_region_name":"7","feature_type":"variation","strand":1,"end":140595651,"alleles":["C","A","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595651},{"clinical_significance":[],"seq_region_name":"7","id":"rs1268129913","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595652,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140595652},{"seq_region_name":"7","id":"rs2130672185","clinical_significance":[],"strand":1,"feature_type":"variation","end":140595653,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595653,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1015171671","seq_region_name":"7","source":"dbSNP","start":140595661,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140595661,"feature_type":"variation","strand":1},{"id":"rs912866980","seq_region_name":"7","clinical_significance":[],"start":140595662,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140595662,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs902126020","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140595663,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595663},{"clinical_significance":[],"seq_region_name":"7","id":"rs866838827","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595664,"feature_type":"variation","strand":1,"end":140595664,"alleles":["G","C"]},{"clinical_significance":[],"id":"rs2130672230","seq_region_name":"7","feature_type":"variation","strand":1,"end":140595667,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595667},{"seq_region_name":"7","id":"rs775935521","clinical_significance":[],"alleles":["C","T"],"end":140595668,"strand":1,"feature_type":"variation","start":140595668,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs997680300","clinical_significance":[],"start":140595669,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140595669,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1321383982","clinical_significance":[],"end":140595672,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140595672,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140595673,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140595673,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs949794670"},{"end":140595675,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140595675,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs573821793"},{"seq_region_name":"7","id":"rs1326124137","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595680,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140595680},{"seq_region_name":"7","id":"rs1799255115","clinical_significance":[],"alleles":["C","T"],"end":140595683,"strand":1,"feature_type":"variation","start":140595683,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs2130672275","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140595684,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595684,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs981167530","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595689,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140595689},{"seq_region_name":"7","id":"rs927174538","clinical_significance":[],"start":140595691,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140595691,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595692,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140595692,"seq_region_name":"7","id":"rs1029598219","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799255577","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595697,"feature_type":"variation","strand":1,"end":140595697,"alleles":["G","T"]},{"source":"dbSNP","start":140595699,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140595699,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799255697"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140595700,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595700,"clinical_significance":[],"id":"rs1799255798","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1284418975","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595705,"feature_type":"variation","strand":1,"end":140595705,"alleles":["T","C","G"]},{"clinical_significance":[],"id":"rs937159711","seq_region_name":"7","feature_type":"variation","strand":1,"end":140595707,"alleles":["G","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595707},{"id":"rs1799256234","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595711,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140595711},{"source":"dbSNP","start":140595712,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140595712,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1400095199"},{"strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140595720,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595720,"source":"dbSNP","seq_region_name":"7","id":"rs1799256466","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799256584","end":140595722,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140595722,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1585720303","clinical_significance":[],"end":140595725,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140595725,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1312820621","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140595732,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595732},{"id":"rs1799256911","seq_region_name":"7","clinical_significance":[],"end":140595733,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140595733,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140595735,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595735,"source":"dbSNP","seq_region_name":"7","id":"rs1430881804","clinical_significance":[]},{"end":140595737,"alleles":["CC","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140595736,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799257133"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595737,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140595737,"clinical_significance":[],"seq_region_name":"7","id":"rs1799257248"},{"feature_type":"variation","strand":1,"end":140595738,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595738,"clinical_significance":[],"seq_region_name":"7","id":"rs541245142"},{"end":140595743,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140595743,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799257477"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595747,"feature_type":"variation","strand":1,"end":140595747,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs150511939"},{"clinical_significance":[],"id":"rs868869016","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595749,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140595749},{"strand":1,"feature_type":"variation","end":140595754,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595754,"source":"dbSNP","seq_region_name":"7","id":"rs533148477","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595759,"feature_type":"variation","strand":1,"end":140595759,"alleles":["C","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1425054987"},{"source":"dbSNP","start":140595760,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140595760,"alleles":["C","A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs375114670"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1477709659","source":"dbSNP","start":140595762,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140595762,"alleles":["T","C"],"feature_type":"variation","strand":1},{"id":"rs1585720386","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595763,"source":"dbSNP","strand":1,"feature_type":"variation","end":140595763,"alleles":["G","T"]},{"alleles":["T","C"],"end":140595764,"strand":1,"feature_type":"variation","start":140595764,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1276664212","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595767,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","T"],"end":140595767,"seq_region_name":"7","id":"rs1247187293","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595767,"source":"dbSNP","strand":1,"feature_type":"variation","end":140595779,"alleles":["AAAAAAAAAAAAA","AAAAAAAA","AAAAAAAAAAA","AAAAAAAAAAAA","AAAAAAAAAAAAAA"],"seq_region_name":"7","id":"rs957024730","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799259136","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595770,"source":"dbSNP","strand":1,"feature_type":"variation","end":140595770,"alleles":["A","C"]},{"alleles":["AA","G"],"end":140595773,"feature_type":"variation","strand":1,"source":"dbSNP","start":140595772,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs373461203","seq_region_name":"7"},{"id":"rs988510285","seq_region_name":"7","clinical_significance":[],"start":140595773,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140595773,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"start":140595773,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140595774,"alleles":["AA","G"],"strand":1,"feature_type":"variation","id":"rs1554476881","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595778,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140595778,"seq_region_name":"7","id":"rs929859593","clinical_significance":[]},{"seq_region_name":"7","id":"rs76481618","clinical_significance":[],"strand":1,"feature_type":"variation","end":140595779,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595779,"source":"dbSNP"},{"id":"rs79473502","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140595780,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595780,"source":"dbSNP"},{"start":140595781,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140595781,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1292815861","clinical_significance":[]},{"source":"dbSNP","start":140595785,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140595785,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1410497974","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140595787,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595787,"source":"dbSNP","seq_region_name":"7","id":"rs1352913178","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1306679332","end":140595792,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140595792,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1200727316","end":140595794,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140595794,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140595796,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140595796,"alleles":["A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799260643","clinical_significance":[]},{"start":140595797,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140595797,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1409777825","clinical_significance":[]},{"alleles":["C","G","T"],"end":140595802,"strand":1,"feature_type":"variation","start":140595802,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs886416035","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs368744358","source":"dbSNP","start":140595803,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140595803,"alleles":["G","A","T"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595806,"feature_type":"variation","strand":1,"end":140595806,"alleles":["C","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs28513390"},{"clinical_significance":[],"id":"rs1799261370","seq_region_name":"7","source":"dbSNP","start":140595807,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140595807,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799261486","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140595811,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595811},{"seq_region_name":"7","id":"rs900702632","clinical_significance":[],"alleles":["A","G"],"end":140595814,"strand":1,"feature_type":"variation","start":140595814,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799261685","end":140595818,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140595818,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595819,"feature_type":"variation","strand":1,"end":140595819,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1415193125"},{"start":140595823,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140595823,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799261906","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140595825,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595825,"source":"dbSNP","seq_region_name":"7","id":"rs1799262013","clinical_significance":[]},{"seq_region_name":"7","id":"rs1172054248","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595842,"source":"dbSNP","strand":1,"feature_type":"variation","end":140595842,"alleles":["G","A","T"]},{"alleles":["A","G"],"end":140595843,"strand":1,"feature_type":"variation","start":140595843,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799262460","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140595847,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595847,"clinical_significance":[],"seq_region_name":"7","id":"rs1385844868"},{"clinical_significance":[],"seq_region_name":"7","id":"rs747536736","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595849,"feature_type":"variation","strand":1,"end":140595849,"alleles":["C","T"]},{"clinical_significance":[],"id":"rs1799262804","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595850,"feature_type":"variation","strand":1,"end":140595850,"alleles":["G","A","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595851,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140595851,"clinical_significance":[],"id":"rs981276483","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1316527694","clinical_significance":[],"alleles":["G","A","T"],"end":140595852,"strand":1,"feature_type":"variation","start":140595852,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140595857,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595857,"clinical_significance":[],"seq_region_name":"7","id":"rs1359616871"},{"seq_region_name":"7","id":"rs1799263299","clinical_significance":[],"start":140595859,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140595859,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140595863,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TCCTCCTCCTCC","TCCTCCTCCTCCTCC"],"end":140595874,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799263416"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799263521","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595864,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140595864},{"seq_region_name":"7","id":"rs530968228","clinical_significance":[],"start":140595866,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140595866,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595867,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140595867,"id":"rs1799263737","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595868,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140595868,"clinical_significance":[],"seq_region_name":"7","id":"rs769006708"},{"strand":1,"feature_type":"variation","end":140595872,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595872,"source":"dbSNP","id":"rs1354579331","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595874,"source":"dbSNP","strand":1,"feature_type":"variation","end":140595874,"alleles":["C","T"],"id":"rs1033142971","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs957618563","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140595876,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595876},{"start":140595879,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140595879,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs549073307","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs937394259","source":"dbSNP","start":140595882,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AGAG","AG"],"end":140595885,"feature_type":"variation","strand":1},{"start":140595884,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140595884,"alleles":["A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799264556","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595885,"source":"dbSNP","strand":1,"feature_type":"variation","end":140595885,"alleles":["G","A"],"id":"rs1799264663","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799264782","clinical_significance":[],"start":140595894,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140595894,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799264914","alleles":["T","C"],"end":140595896,"feature_type":"variation","strand":1,"source":"dbSNP","start":140595896,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1352367582","clinical_significance":[],"end":140595897,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140595897,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140595900,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140595900,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs944088454"},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140595901,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595901,"clinical_significance":[],"id":"rs1010464244","seq_region_name":"7"},{"seq_region_name":"7","id":"rs2130672822","clinical_significance":[],"start":140595907,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140595907,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140595909,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140595909,"alleles":["T","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1442033896"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1332180204","source":"dbSNP","start":140595910,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140595910,"alleles":["G","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs567970691","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595915,"source":"dbSNP","strand":1,"feature_type":"variation","end":140595915,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1385434901","alleles":["G","A"],"end":140595916,"feature_type":"variation","strand":1,"source":"dbSNP","start":140595916,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140595918,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140595918,"alleles":["C","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs528733072","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799265915","clinical_significance":[],"alleles":["CAGCTCTTCCCCATGGCTCGCCATACTCAGGAAGGGC","CAGCTCTTCCCCATGGCTCGCCATACTCAGGAAGGGCCAGCTCTTCCCCATGGCTCGCCATACTCAGGAAGGGC"],"end":140595954,"strand":1,"feature_type":"variation","start":140595918,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595925,"feature_type":"variation","strand":1,"end":140595925,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs547180977"},{"clinical_significance":[],"seq_region_name":"7","id":"rs887899683","feature_type":"variation","strand":1,"end":140595926,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595926},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585720770","feature_type":"variation","strand":1,"end":140595930,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595930},{"seq_region_name":"7","id":"rs1799266521","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595933,"source":"dbSNP","strand":1,"feature_type":"variation","end":140595933,"alleles":["G","T"]},{"start":140595936,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140595936,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs1799266656","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs940686026","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595937,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140595937},{"seq_region_name":"7","id":"rs1799266905","clinical_significance":[],"strand":1,"feature_type":"variation","end":140595941,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595941,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1457333505","source":"dbSNP","start":140595948,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140595948,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1036798612","feature_type":"variation","strand":1,"end":140595950,"alleles":["AA","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595949},{"seq_region_name":"7","id":"rs1799267257","clinical_significance":[],"alleles":["G","A"],"end":140595951,"strand":1,"feature_type":"variation","start":140595951,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["G","A"],"end":140595952,"feature_type":"variation","strand":1,"source":"dbSNP","start":140595952,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799267365"},{"id":"rs191843316","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140595954,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595954,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140595956,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595956,"source":"dbSNP","seq_region_name":"7","id":"rs1585720824","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799267710","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140595958,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595958},{"end":140595962,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140595962,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799267820"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140595963,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595963,"source":"dbSNP","seq_region_name":"7","id":"rs1799267936","clinical_significance":[]},{"seq_region_name":"7","id":"rs981245246","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595965,"source":"dbSNP","strand":1,"feature_type":"variation","end":140595965,"alleles":["C","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1469623943","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140595973,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595973},{"seq_region_name":"7","id":"rs1799268291","clinical_significance":[],"strand":1,"feature_type":"variation","end":140595974,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595974,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799268381","clinical_significance":[],"start":140595975,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140595975,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140595977,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140595977,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs927030040"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595982,"source":"dbSNP","strand":1,"feature_type":"variation","end":140595982,"alleles":["G","A"],"seq_region_name":"7","id":"rs1247202384","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595983,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140595983,"clinical_significance":[],"seq_region_name":"7","id":"rs776864338"},{"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140595984,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595984,"source":"dbSNP","id":"rs762092669","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140595992,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140595992,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130673014"},{"start":140595992,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140595993,"alleles":["AG","-"],"strand":1,"feature_type":"variation","id":"rs1799269016","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140595992,"feature_type":"variation","strand":1,"end":140595999,"alleles":["AGGAGGAG","AGGAG"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799269126"},{"seq_region_name":"7","id":"rs1799269223","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595993,"source":"dbSNP","strand":1,"feature_type":"variation","end":140595993,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1799269332","clinical_significance":[],"end":140595994,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140595994,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1585720897","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140595995,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595995,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140595997,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140595997,"source":"dbSNP","seq_region_name":"7","id":"rs1799269569","clinical_significance":[]},{"alleles":["A","G"],"end":140595998,"strand":1,"feature_type":"variation","start":140595998,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585720910","clinical_significance":[]},{"start":140595999,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140595999,"strand":1,"feature_type":"variation","id":"rs1799269786","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1209537521","source":"dbSNP","start":140596005,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140596005,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs117900988","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596006,"feature_type":"variation","strand":1,"end":140596006,"alleles":["G","A","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799270162","source":"dbSNP","start":140596008,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140596008,"alleles":["T","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1799270275","clinical_significance":[],"alleles":["G","C","T"],"end":140596010,"strand":1,"feature_type":"variation","start":140596010,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140596016,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140596016,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799270422"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1284902087","source":"dbSNP","start":140596024,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140596024,"alleles":["T","G"],"feature_type":"variation","strand":1},{"id":"rs1799270649","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["TCTGTTATCGGGTAACTCCTC","TC"],"end":140596045,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596025,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1223283902","clinical_significance":[],"end":140596028,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140596028,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596033,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140596033,"clinical_significance":[],"id":"rs889294945","seq_region_name":"7"},{"source":"dbSNP","start":140596034,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140596034,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1223658202"},{"alleles":["GGG","GGGG"],"end":140596036,"feature_type":"variation","strand":1,"source":"dbSNP","start":140596034,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799271137","seq_region_name":"7"},{"alleles":["G","A"],"end":140596035,"strand":1,"feature_type":"variation","start":140596035,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs775899405","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1324816499","alleles":["T","C"],"end":140596037,"feature_type":"variation","strand":1,"source":"dbSNP","start":140596037,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140596039,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140596039,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799271516","clinical_significance":[]},{"end":140596046,"alleles":["CTCCTCC","CTCC"],"strand":1,"feature_type":"variation","start":140596040,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1006605437","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","C"],"end":140596044,"strand":1,"feature_type":"variation","start":140596044,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1032755112","clinical_significance":[]},{"end":140596046,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140596046,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs929911853","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1046944055","end":140596047,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140596047,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140596049,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","T"],"end":140596049,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs572553329","clinical_significance":[]},{"start":140596050,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140596050,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1563166973","clinical_significance":[]},{"end":140596054,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140596054,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs149283386","clinical_significance":[]},{"id":"rs1425830935","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140596055,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596055,"source":"dbSNP"},{"start":140596057,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140596057,"strand":1,"feature_type":"variation","id":"rs1799272546","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1174206051","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596058,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140596058},{"seq_region_name":"7","id":"rs1799272780","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140596060,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596060,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs944700121","source":"dbSNP","start":140596063,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140596063,"alleles":["A","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs763169039","clinical_significance":[],"start":140596067,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140596067,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140596069,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140596069,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1020390411"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596070,"feature_type":"variation","strand":1,"alleles":["GGG","GG"],"end":140596072,"clinical_significance":[],"seq_region_name":"7","id":"rs1799273092"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1188969398","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596071,"feature_type":"variation","strand":1,"end":140596071,"alleles":["G","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799273448","end":140596087,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140596087,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1466467422","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596088,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140596088},{"start":140596093,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140596093,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1240556982","clinical_significance":[]},{"alleles":["C","A"],"end":140596102,"strand":1,"feature_type":"variation","start":140596102,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1471218651","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799273958","clinical_significance":[],"start":140596103,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140596103,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140596109,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596109,"clinical_significance":[],"seq_region_name":"7","id":"rs1799274144"},{"alleles":["C","T"],"end":140596112,"strand":1,"feature_type":"variation","start":140596112,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1799274280","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799274437","clinical_significance":[],"alleles":["A","C"],"end":140596113,"strand":1,"feature_type":"variation","start":140596113,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799274607","feature_type":"variation","strand":1,"alleles":["A","T"],"end":140596120,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596120},{"feature_type":"variation","strand":1,"end":140596121,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596121,"clinical_significance":[],"seq_region_name":"7","id":"rs1799274759"},{"seq_region_name":"7","id":"rs971312132","clinical_significance":[],"alleles":["A","G"],"end":140596126,"strand":1,"feature_type":"variation","start":140596126,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799275166","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140596129,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596129},{"feature_type":"variation","strand":1,"end":140596130,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596130,"clinical_significance":[],"seq_region_name":"7","id":"rs1040501985"},{"alleles":["T","C"],"end":140596131,"feature_type":"variation","strand":1,"source":"dbSNP","start":140596131,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799275506"},{"end":140596133,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140596133,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1799275683","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1281376164","clinical_significance":[],"alleles":["C","A"],"end":140596134,"strand":1,"feature_type":"variation","start":140596134,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["A","G"],"end":140596139,"feature_type":"variation","strand":1,"source":"dbSNP","start":140596139,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799276046","seq_region_name":"7"},{"alleles":["T","C"],"end":140596141,"feature_type":"variation","strand":1,"source":"dbSNP","start":140596141,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799276208","seq_region_name":"7"},{"end":140596148,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140596148,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1232670360","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799276516","alleles":["C","T"],"end":140596153,"feature_type":"variation","strand":1,"source":"dbSNP","start":140596153,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1347611993","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596157,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140596157},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596158,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140596158,"id":"rs981776162","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1231053347","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596164,"feature_type":"variation","strand":1,"end":140596164,"alleles":["C","T"]},{"clinical_significance":[],"id":"rs1363698819","seq_region_name":"7","source":"dbSNP","start":140596167,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140596167,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs900586821","clinical_significance":[],"end":140596173,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140596173,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1429449805","alleles":["T","C"],"end":140596174,"feature_type":"variation","strand":1,"source":"dbSNP","start":140596174,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596177,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140596177,"id":"rs1799277242","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1425601649","source":"dbSNP","start":140596183,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C","G"],"end":140596183,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596185,"feature_type":"variation","strand":1,"end":140596185,"alleles":["A","G"],"clinical_significance":[],"id":"rs996241842","seq_region_name":"7"},{"end":140596187,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140596187,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799277589"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1336100116","source":"dbSNP","start":140596205,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140596205,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1432862277","source":"dbSNP","start":140596231,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140596231,"alleles":["G","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1304730466","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596232,"feature_type":"variation","strand":1,"end":140596232,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799278045","source":"dbSNP","start":140596234,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140596234,"alleles":["C","T"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596235,"source":"dbSNP","strand":1,"feature_type":"variation","end":140596235,"alleles":["C","A","T"],"seq_region_name":"7","id":"rs1055045575","clinical_significance":[]},{"seq_region_name":"7","id":"rs533133902","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140596236,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596236,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1417676298","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596239,"feature_type":"variation","strand":1,"end":140596239,"alleles":["T","G"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596252,"source":"dbSNP","strand":1,"feature_type":"variation","end":140596252,"alleles":["A","G"],"seq_region_name":"7","id":"rs1186101954","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140596256,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596256,"source":"dbSNP","id":"rs1799278640","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130673538","source":"dbSNP","start":140596257,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140596257,"alleles":["G","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs984620640","clinical_significance":[],"start":140596258,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140596258,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140596263,"alleles":["A","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596263,"clinical_significance":[],"seq_region_name":"7","id":"rs1239212754"},{"seq_region_name":"7","id":"rs1799279000","clinical_significance":[],"alleles":["T","C"],"end":140596265,"strand":1,"feature_type":"variation","start":140596265,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140596276,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596276,"source":"dbSNP","seq_region_name":"7","id":"rs909285659","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596277,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140596277,"clinical_significance":[],"id":"rs940800706","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140596280,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596280,"source":"dbSNP","seq_region_name":"7","id":"rs1799279406","clinical_significance":[]},{"seq_region_name":"7","id":"rs1207785400","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596282,"source":"dbSNP","strand":1,"feature_type":"variation","end":140596282,"alleles":["C","A"]},{"alleles":["AAA","AA"],"end":140596286,"feature_type":"variation","strand":1,"source":"dbSNP","start":140596284,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799279625"},{"alleles":["T","A"],"end":140596287,"strand":1,"feature_type":"variation","start":140596287,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585721415","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1306084134","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596292,"feature_type":"variation","strand":1,"end":140596292,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1036339990","end":140596295,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140596295,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1213563001","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140596297,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596297,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799280210","clinical_significance":[],"alleles":["A","G"],"end":140596298,"strand":1,"feature_type":"variation","start":140596298,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140596301,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140596301,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1379443458"},{"seq_region_name":"7","id":"rs1799280430","clinical_significance":[],"strand":1,"feature_type":"variation","end":140596314,"alleles":["AGTAG","AG"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596310,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140596319,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596319,"clinical_significance":[],"seq_region_name":"7","id":"rs1799280532"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799280625","end":140596321,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140596321,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1294660396","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596323,"feature_type":"variation","strand":1,"end":140596323,"alleles":["C","T"]},{"alleles":["C","T"],"end":140596328,"feature_type":"variation","strand":1,"source":"dbSNP","start":140596328,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799280832"},{"source":"dbSNP","start":140596332,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140596332,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1412365205"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1354792558","alleles":["A","G"],"end":140596333,"feature_type":"variation","strand":1,"source":"dbSNP","start":140596333,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["AATCAA","AA"],"end":140596342,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596337,"source":"dbSNP","seq_region_name":"7","id":"rs1799281145","clinical_significance":[]},{"end":140596346,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140596346,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1336972440","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799281385","clinical_significance":[],"alleles":["T","C"],"end":140596347,"strand":1,"feature_type":"variation","start":140596347,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1799281503","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596348,"feature_type":"variation","strand":1,"end":140596348,"alleles":["G","A"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596349,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140596349,"clinical_significance":[],"id":"rs144537424","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140596350,"alleles":["G","A","C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596350,"source":"dbSNP","seq_region_name":"7","id":"rs753066679","clinical_significance":[]},{"source":"dbSNP","start":140596351,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140596351,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1010518380"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1359690363","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596352,"feature_type":"variation","strand":1,"end":140596352,"alleles":["T","C"]},{"id":"rs1799282093","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140596358,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596358,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1799282197","seq_region_name":"7","source":"dbSNP","start":140596360,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140596360,"alleles":["A","G"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140596362,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596362,"clinical_significance":[],"seq_region_name":"7","id":"rs1799282394"},{"seq_region_name":"7","id":"rs1799282561","clinical_significance":[],"end":140596364,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140596364,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140596366,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140596366,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs542973935"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596372,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140596372,"clinical_significance":[],"seq_region_name":"7","id":"rs1799282905"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799283094","feature_type":"variation","strand":1,"end":140596375,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596375},{"alleles":["G","A"],"end":140596376,"feature_type":"variation","strand":1,"source":"dbSNP","start":140596376,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1170015629"},{"id":"rs1799283450","seq_region_name":"7","clinical_significance":[],"end":140596378,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140596378,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140596381,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140596381,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs139342202","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1002952336","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140596385,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596385,"source":"dbSNP"},{"seq_region_name":"7","id":"rs555014254","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140596386,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596386,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1253202157","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596387,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140596387},{"seq_region_name":"7","id":"rs1184901152","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596390,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140596390},{"seq_region_name":"7","id":"rs1479869006","clinical_significance":[],"end":140596392,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140596392,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["C","A","T"],"end":140596396,"strand":1,"feature_type":"variation","start":140596396,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1209724593","clinical_significance":[]},{"seq_region_name":"7","id":"rs573897619","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596397,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140596397},{"clinical_significance":[],"id":"rs958711478","seq_region_name":"7","alleles":["T","G"],"end":140596400,"feature_type":"variation","strand":1,"source":"dbSNP","start":140596400,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1440107096","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140596408,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596408},{"seq_region_name":"7","id":"rs973824584","clinical_significance":[],"alleles":["G","T"],"end":140596410,"strand":1,"feature_type":"variation","start":140596410,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1799284960","clinical_significance":[],"alleles":["T","A"],"end":140596412,"strand":1,"feature_type":"variation","start":140596412,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140596414,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140596414,"alleles":["C","A"],"strand":1,"feature_type":"variation","id":"rs1274634968","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1230957466","end":140596415,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140596415,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1001022486","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596417,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140596417},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140596425,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596425,"source":"dbSNP","seq_region_name":"7","id":"rs919782155","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596428,"source":"dbSNP","strand":1,"feature_type":"variation","end":140596428,"alleles":["A","C"],"id":"rs1563167138","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596430,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140596430,"seq_region_name":"7","id":"rs1799285613","clinical_significance":[]},{"start":140596432,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140596432,"alleles":["A","G"],"strand":1,"feature_type":"variation","id":"rs1799285726","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799285841","source":"dbSNP","start":140596442,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140596442,"alleles":["G","T"],"feature_type":"variation","strand":1},{"id":"rs1288926078","seq_region_name":"7","clinical_significance":[],"start":140596443,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140596443,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1585721748","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596448,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140596448},{"id":"rs1053982445","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596451,"source":"dbSNP","strand":1,"feature_type":"variation","end":140596451,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs951204383","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596454,"feature_type":"variation","strand":1,"end":140596454,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs1585721790","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596461,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140596461},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596463,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140596463,"id":"rs1799286523","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140596469,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596469,"source":"dbSNP","seq_region_name":"7","id":"rs1585721802","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140596470,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596470,"clinical_significance":[],"seq_region_name":"7","id":"rs1799286748"},{"seq_region_name":"7","id":"rs892868763","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596477,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140596477},{"source":"dbSNP","start":140596479,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140596479,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799286976"},{"start":140596481,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140596481,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs982696873","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140596482,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596482,"clinical_significance":[],"seq_region_name":"7","id":"rs912475960"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140596489,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596489,"source":"dbSNP","seq_region_name":"7","id":"rs2130674039","clinical_significance":[]},{"alleles":["G","T"],"end":140596492,"feature_type":"variation","strand":1,"source":"dbSNP","start":140596492,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs943929642"},{"seq_region_name":"7","id":"rs766602553","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596493,"source":"dbSNP","strand":1,"feature_type":"variation","end":140596493,"alleles":["C","G"]},{"start":140596494,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","T"],"end":140596494,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799287807","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140596497,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596497,"clinical_significance":[],"seq_region_name":"7","id":"rs555211635"},{"seq_region_name":"7","id":"rs534648045","clinical_significance":[],"strand":1,"feature_type":"variation","end":140596502,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596502,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1002584699","feature_type":"variation","strand":1,"end":140596503,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596503},{"feature_type":"variation","strand":1,"end":140596509,"alleles":["T","C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596509,"clinical_significance":[],"seq_region_name":"7","id":"rs1412720857"},{"seq_region_name":"7","id":"rs752619817","clinical_significance":[],"start":140596517,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140596517,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596518,"feature_type":"variation","strand":1,"end":140596518,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1457243472"},{"alleles":["A","G"],"end":140596520,"strand":1,"feature_type":"variation","start":140596520,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1250409933","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140596523,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596523,"source":"dbSNP","seq_region_name":"7","id":"rs1192181273","clinical_significance":[]},{"clinical_significance":[],"id":"rs958642674","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","A"],"end":140596525,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596525},{"end":140596526,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140596526,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799288889"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799289065","alleles":["C","T"],"end":140596527,"feature_type":"variation","strand":1,"source":"dbSNP","start":140596527,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs932078443","clinical_significance":[],"start":140596530,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140596530,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140596532,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140596532,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs371026252"},{"source":"dbSNP","start":140596533,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140596533,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799289670","seq_region_name":"7"},{"start":140596534,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140596534,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1054528275","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799290019","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140596535,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596535},{"end":140596544,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140596544,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs972564976","clinical_significance":[]},{"source":"dbSNP","start":140596545,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140596545,"alleles":["A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585721977"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596548,"source":"dbSNP","strand":1,"feature_type":"variation","end":140596548,"alleles":["G","C"],"seq_region_name":"7","id":"rs1487731119","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140596554,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596554,"clinical_significance":[],"seq_region_name":"7","id":"rs1398514194"},{"clinical_significance":[],"id":"rs577960783","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596558,"feature_type":"variation","strand":1,"end":140596558,"alleles":["C","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596561,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140596561,"clinical_significance":[],"seq_region_name":"7","id":"rs1306163079"},{"clinical_significance":[],"id":"rs1219618421","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140596564,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596564},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596567,"source":"dbSNP","strand":1,"feature_type":"variation","end":140596567,"alleles":["G","C"],"seq_region_name":"7","id":"rs1799291291","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130674242","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140596569,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596569},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140596570,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596570,"source":"dbSNP","seq_region_name":"7","id":"rs1372842513","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140596572,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596572,"clinical_significance":[],"seq_region_name":"7","id":"rs1799291659"},{"strand":1,"feature_type":"variation","alleles":["GCAGC","GCAGCAGC"],"end":140596579,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596575,"source":"dbSNP","seq_region_name":"7","id":"rs1324151554","clinical_significance":[]},{"seq_region_name":"7","id":"rs1389658768","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140596581,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596581,"source":"dbSNP"},{"seq_region_name":"7","id":"rs923257679","clinical_significance":[],"start":140596584,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A","C"],"end":140596584,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140596587,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140596587,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799292484"},{"source":"dbSNP","start":140596591,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140596591,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799292664"},{"source":"dbSNP","start":140596595,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140596595,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799292845"},{"seq_region_name":"7","id":"rs269241","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596601,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140596601},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140596602,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596602,"clinical_significance":[],"seq_region_name":"7","id":"rs1382892155"},{"clinical_significance":[],"id":"rs1010402393","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596609,"feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140596609},{"end":140596610,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140596610,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1042033494","seq_region_name":"7"},{"id":"rs563783222","seq_region_name":"7","clinical_significance":[],"start":140596611,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140596611,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"start":140596614,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140596614,"alleles":["T","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs144106057","clinical_significance":[]},{"clinical_significance":[],"id":"rs1393590323","seq_region_name":"7","end":140596618,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140596618,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1799294599","clinical_significance":[],"strand":1,"feature_type":"variation","end":140596621,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596621,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596626,"source":"dbSNP","strand":1,"feature_type":"variation","end":140596626,"alleles":["T","C"],"seq_region_name":"7","id":"rs543030390","clinical_significance":[]},{"end":140596627,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140596627,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs910789845","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799295211","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596628,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140596628},{"feature_type":"variation","strand":1,"end":140596635,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596635,"clinical_significance":[],"seq_region_name":"7","id":"rs561091829"},{"clinical_significance":[],"id":"rs538636862","seq_region_name":"7","end":140596636,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140596636,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs2130674400","clinical_significance":[],"start":140596637,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140596637,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs183615354","clinical_significance":[],"strand":1,"feature_type":"variation","end":140596641,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596641,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1053931505","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140596642,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596642,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1342083891","clinical_significance":[],"end":140596645,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140596645,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["A","G"],"end":140596646,"feature_type":"variation","strand":1,"source":"dbSNP","start":140596646,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1197313474"},{"seq_region_name":"7","id":"rs1585722252","clinical_significance":[],"end":140596648,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140596648,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1799296623","clinical_significance":[],"start":140596649,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140596649,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140596652,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140596652,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1484582524"},{"seq_region_name":"7","id":"rs1799296964","clinical_significance":[],"strand":1,"feature_type":"variation","end":140596654,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596654,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799297152","end":140596657,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140596657,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1237586309","seq_region_name":"7","source":"dbSNP","start":140596658,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140596658,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799297482","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140596664,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596664},{"seq_region_name":"7","id":"rs1260096209","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596666,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140596666},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596667,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AAAA","AAA"],"end":140596670,"seq_region_name":"7","id":"rs2130674497","clinical_significance":[]},{"seq_region_name":"7","id":"rs1003096267","clinical_significance":[],"start":140596671,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140596671,"alleles":["T","C","G"],"strand":1,"feature_type":"variation"},{"alleles":["T","A"],"end":140596674,"feature_type":"variation","strand":1,"source":"dbSNP","start":140596674,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1034446524"},{"seq_region_name":"7","id":"rs1301062653","clinical_significance":[],"end":140596676,"alleles":["A","-"],"strand":1,"feature_type":"variation","start":140596676,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1233268215","seq_region_name":"7","feature_type":"variation","strand":1,"end":140596681,"alleles":["A","C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596681},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140596686,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596686,"source":"dbSNP","seq_region_name":"7","id":"rs1799298405","clinical_significance":[]},{"source":"dbSNP","start":140596688,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140596688,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1366250224"},{"seq_region_name":"7","id":"rs1297947180","clinical_significance":[],"start":140596697,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140596697,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140596698,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140596698,"alleles":["T","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799298709"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563167291","feature_type":"variation","strand":1,"end":140596704,"alleles":["C","A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596704},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140596705,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596705,"clinical_significance":[],"seq_region_name":"7","id":"rs1380627674"},{"id":"rs1799299065","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140596709,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596709,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799299188","feature_type":"variation","strand":1,"end":140596711,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596711},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596712,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140596712,"clinical_significance":[],"seq_region_name":"7","id":"rs1799299295"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799299405","source":"dbSNP","start":140596713,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140596713,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140596719,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596719,"source":"dbSNP","id":"rs1799299527","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140596723,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140596723,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799299650"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596724,"source":"dbSNP","strand":1,"feature_type":"variation","end":140596724,"alleles":["G","C","T"],"seq_region_name":"7","id":"rs1009951105","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1185606421","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596725,"feature_type":"variation","strand":1,"end":140596725,"alleles":["A","C"]},{"seq_region_name":"7","id":"rs1041858029","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140596733,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596733,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1173457237","seq_region_name":"7","alleles":["T","C"],"end":140596735,"feature_type":"variation","strand":1,"source":"dbSNP","start":140596735,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140596738,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596738,"source":"dbSNP","seq_region_name":"7","id":"rs2130674635","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs906982980","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596740,"feature_type":"variation","strand":1,"end":140596740,"alleles":["C","T"]},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140596746,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596746,"clinical_significance":[],"seq_region_name":"7","id":"rs2130674659"},{"start":140596761,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140596761,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1373319245","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140596762,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596762,"clinical_significance":[],"seq_region_name":"7","id":"rs1799300586"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596767,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140596767,"clinical_significance":[],"seq_region_name":"7","id":"rs1423507552"},{"seq_region_name":"7","id":"rs894121284","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140596768,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596768,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1799300948","seq_region_name":"7","feature_type":"variation","strand":1,"end":140596774,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596774},{"source":"dbSNP","start":140596777,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140596777,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799301064"},{"start":140596779,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140596779,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130674705","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1426232988","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596780,"feature_type":"variation","strand":1,"alleles":["G","C","T"],"end":140596780},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140596782,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596782,"source":"dbSNP","seq_region_name":"7","id":"rs1260351724","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596789,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140596789,"seq_region_name":"7","id":"rs1799301450","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1033998621","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140596795,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596795},{"strand":1,"feature_type":"variation","end":140596798,"alleles":["T","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596798,"source":"dbSNP","seq_region_name":"7","id":"rs958590501","clinical_significance":[]},{"end":140596798,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140596798,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1278063552","seq_region_name":"7","clinical_significance":[]},{"start":140596799,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140596799,"alleles":["G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130674756","clinical_significance":[]},{"start":140596805,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["-","CTTTATGAA"],"end":140596804,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799301935","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799302063","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596805,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140596805},{"seq_region_name":"7","id":"rs1209928348","clinical_significance":[],"start":140596806,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140596806,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"end":140596814,"alleles":["ATGTGAAT","ATGTGAATGTGAAT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140596807,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799302400","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1374647894","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596809,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140596809},{"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140596810,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596810,"source":"dbSNP","id":"rs1799302783","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1342548649","clinical_significance":[],"start":140596814,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140596814,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs763942900","end":140596816,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140596816,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["T","A"],"end":140596821,"feature_type":"variation","strand":1,"source":"dbSNP","start":140596821,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799303383"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1225438557","feature_type":"variation","strand":1,"end":140596824,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596824},{"seq_region_name":"7","id":"rs1799303744","clinical_significance":[],"alleles":["T","C"],"end":140596827,"strand":1,"feature_type":"variation","start":140596827,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1006106192","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596830,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140596830},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799304166","feature_type":"variation","strand":1,"end":140596831,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596831},{"clinical_significance":[],"id":"rs1799304356","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596831,"feature_type":"variation","strand":1,"alleles":["ACTTA","A"],"end":140596835},{"strand":1,"feature_type":"variation","end":140596835,"alleles":["A","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596835,"source":"dbSNP","seq_region_name":"7","id":"rs1799304530","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140596840,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596840,"clinical_significance":[],"seq_region_name":"7","id":"rs1416672997"},{"source":"dbSNP","start":140596841,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140596841,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs10270711"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1312758488","alleles":["G","A"],"end":140596843,"feature_type":"variation","strand":1,"source":"dbSNP","start":140596843,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140596844,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140596844,"strand":1,"feature_type":"variation","id":"rs1799305280","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","C"],"end":140596846,"strand":1,"feature_type":"variation","start":140596846,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799305384","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1406126723","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140596847,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596847},{"seq_region_name":"7","id":"rs1799305614","clinical_significance":[],"alleles":["G","A"],"end":140596855,"strand":1,"feature_type":"variation","start":140596855,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["A","G"],"end":140596860,"strand":1,"feature_type":"variation","start":140596860,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs565233872","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs982582303","alleles":["G","A"],"end":140596862,"feature_type":"variation","strand":1,"source":"dbSNP","start":140596862,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs532607866","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140596864,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596864,"source":"dbSNP"},{"id":"rs544254362","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596865,"source":"dbSNP","strand":1,"feature_type":"variation","end":140596865,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs562467307","clinical_significance":[],"start":140596866,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140596866,"alleles":["G","A","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1296655969","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140596867,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596867,"source":"dbSNP"},{"id":"rs1799306474","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596870,"source":"dbSNP","strand":1,"feature_type":"variation","end":140596870,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1799306571","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596886,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140596886},{"id":"rs1165066131","seq_region_name":"7","clinical_significance":[],"start":140596894,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140596894,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1799306782","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596897,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140596897},{"end":140596898,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140596898,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1475880345"},{"id":"rs954841146","seq_region_name":"7","clinical_significance":[],"end":140596905,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140596905,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1187066459","seq_region_name":"7","clinical_significance":[],"start":140596907,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140596907,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"id":"rs1438192665","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596915,"source":"dbSNP","strand":1,"feature_type":"variation","end":140596915,"alleles":["T","C"]},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140596918,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596918,"source":"dbSNP","seq_region_name":"7","id":"rs1799307341","clinical_significance":[]},{"seq_region_name":"7","id":"rs1252493084","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140596920,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596920,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs376979861","source":"dbSNP","start":140596924,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140596924,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1563167394","clinical_significance":[],"start":140596929,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140596929,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"end":140596937,"alleles":["TGTTGTTGT","TGTTGT"],"strand":1,"feature_type":"variation","start":140596929,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1193846444","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596934,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140596934,"seq_region_name":"7","id":"rs10270838","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["TT","T"],"end":140596935,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596934,"source":"dbSNP","seq_region_name":"7","id":"rs1339040039","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596937,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140596937,"clinical_significance":[],"id":"rs1799308228","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs931989759","end":140596943,"alleles":["C","A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140596943,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1799308496","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140596944,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596944,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1258009885","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140596945,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140596945,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140596952,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596952,"clinical_significance":[],"seq_region_name":"7","id":"rs1799308717"},{"start":140596958,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140596958,"alleles":["T","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1332700330","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799308964","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596961,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140596961},{"seq_region_name":"7","id":"rs750106695","clinical_significance":[],"alleles":["G","T"],"end":140596974,"strand":1,"feature_type":"variation","start":140596974,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140596977,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140596977,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1324930650"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1205615191","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596980,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140596980},{"clinical_significance":[],"seq_region_name":"7","id":"rs936871851","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596988,"feature_type":"variation","strand":1,"end":140596988,"alleles":["A","G","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596995,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140596995,"clinical_significance":[],"id":"rs1327335919","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799309665","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140596997,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140596997},{"source":"dbSNP","start":140596997,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TT","TTT"],"end":140596998,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799309779"},{"source":"dbSNP","start":140597004,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140597004,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs757855740"},{"clinical_significance":[],"seq_region_name":"7","id":"rs779553970","source":"dbSNP","start":140597009,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140597009,"alleles":["G","A"],"feature_type":"variation","strand":1},{"alleles":["T","A"],"end":140597019,"strand":1,"feature_type":"variation","start":140597019,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1799310127","seq_region_name":"7","clinical_significance":[]},{"start":140597026,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140597026,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs1799310236","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","C"],"end":140597028,"feature_type":"variation","strand":1,"source":"dbSNP","start":140597028,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799310339","seq_region_name":"7"},{"alleles":["G","C"],"end":140597030,"feature_type":"variation","strand":1,"source":"dbSNP","start":140597030,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1483044421"},{"seq_region_name":"7","id":"rs1395368551","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597031,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140597031},{"strand":1,"feature_type":"variation","end":140597037,"alleles":["A","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597037,"source":"dbSNP","seq_region_name":"7","id":"rs1563167446","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799310803","clinical_significance":[],"start":140597041,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140597041,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799310937","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597045,"feature_type":"variation","strand":1,"end":140597045,"alleles":["G","A"]},{"clinical_significance":[],"id":"rs1165135947","seq_region_name":"7","feature_type":"variation","strand":1,"end":140597050,"alleles":["GAAGAA","GAA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597045},{"seq_region_name":"7","id":"rs989732182","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140597046,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597046,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799311284","feature_type":"variation","strand":1,"alleles":["AAA","AA"],"end":140597051,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597049},{"clinical_significance":[],"seq_region_name":"7","id":"rs1263512735","source":"dbSNP","start":140597052,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140597052,"alleles":["G","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1163582198","clinical_significance":[],"alleles":["G","A"],"end":140597057,"strand":1,"feature_type":"variation","start":140597057,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140597063,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140597063,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs34623745","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597067,"feature_type":"variation","strand":1,"end":140597067,"alleles":["C","T"],"clinical_significance":[],"id":"rs1799311775","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597068,"source":"dbSNP","strand":1,"feature_type":"variation","end":140597068,"alleles":["A","G"],"seq_region_name":"7","id":"rs1365445391","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140597069,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597069,"clinical_significance":[],"id":"rs2130675241","seq_region_name":"7"},{"clinical_significance":[],"id":"rs946077165","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140597070,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597070},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140597071,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597071,"source":"dbSNP","seq_region_name":"7","id":"rs1476736790","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799312200","clinical_significance":[],"alleles":["G","C"],"end":140597073,"strand":1,"feature_type":"variation","start":140597073,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1192721418","feature_type":"variation","strand":1,"end":140597077,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597077},{"id":"rs1041919082","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597079,"source":"dbSNP","strand":1,"feature_type":"variation","end":140597079,"alleles":["G","A"]},{"id":"rs1215720759","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597080,"source":"dbSNP","strand":1,"feature_type":"variation","end":140597080,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs747450571","clinical_significance":[],"strand":1,"feature_type":"variation","end":140597081,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597081,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1481411303","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597085,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140597085},{"end":140597090,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140597090,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1585722989","seq_region_name":"7"},{"source":"dbSNP","start":140597091,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140597091,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1272696228"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597094,"feature_type":"variation","strand":1,"end":140597094,"alleles":["G","A","T"],"clinical_significance":[],"id":"rs907342800","seq_region_name":"7"},{"start":140597098,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140597098,"strand":1,"feature_type":"variation","id":"rs1278256079","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799313338","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597105,"source":"dbSNP","strand":1,"feature_type":"variation","end":140597105,"alleles":["G","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799313449","end":140597106,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140597106,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["AGAGA","AGA"],"end":140597112,"strand":1,"feature_type":"variation","start":140597108,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1046590674","clinical_significance":[]},{"clinical_significance":[],"id":"rs1585723025","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140597110,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597110},{"id":"rs1331983885","seq_region_name":"7","clinical_significance":[],"end":140597112,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","start":140597112,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799313931","end":140597113,"alleles":["AA","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140597112,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597114,"source":"dbSNP","strand":1,"feature_type":"variation","end":140597119,"alleles":["GAGGAG","GAG"],"seq_region_name":"7","id":"rs1442739914","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140597117,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597117,"source":"dbSNP","seq_region_name":"7","id":"rs938954660","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140597118,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597118,"clinical_significance":[],"seq_region_name":"7","id":"rs1378602024"},{"clinical_significance":[],"id":"rs1391824657","seq_region_name":"7","feature_type":"variation","strand":1,"end":140597120,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597120},{"alleles":["A","T"],"end":140597123,"strand":1,"feature_type":"variation","start":140597123,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1056035277","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140597124,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140597124,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799314537"},{"start":140597127,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AAAAGAA","AA"],"end":140597133,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799314650","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799314764","clinical_significance":[],"end":140597135,"alleles":["AAGAAGA","AAGA"],"strand":1,"feature_type":"variation","start":140597129,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs536717316","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597132,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140597132},{"id":"rs1400754654","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597133,"source":"dbSNP","strand":1,"feature_type":"variation","end":140597133,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1358079314","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597134,"feature_type":"variation","strand":1,"end":140597134,"alleles":["G","A"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597138,"feature_type":"variation","strand":1,"end":140597138,"alleles":["G","A"],"clinical_significance":[],"id":"rs1799315206","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs938465948","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597145,"feature_type":"variation","strand":1,"end":140597145,"alleles":["A","C"]},{"seq_region_name":"7","id":"rs1799315404","clinical_significance":[],"start":140597149,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140597149,"strand":1,"feature_type":"variation"},{"alleles":["A","G"],"end":140597155,"strand":1,"feature_type":"variation","start":140597155,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1453948701","clinical_significance":[]},{"seq_region_name":"7","id":"rs995179606","clinical_significance":[],"start":140597166,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","T"],"end":140597166,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1290291898","clinical_significance":[],"end":140597167,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140597167,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140597168,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140597168,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1026568790","clinical_significance":[]},{"clinical_significance":[],"id":"rs146509545","seq_region_name":"7","end":140597170,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140597170,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs10261630","seq_region_name":"7","clinical_significance":[],"start":140597179,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140597179,"strand":1,"feature_type":"variation"},{"id":"rs1452869990","seq_region_name":"7","clinical_significance":[],"start":140597180,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140597180,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140597181,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597181,"clinical_significance":[],"seq_region_name":"7","id":"rs1346678621"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597186,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140597186,"seq_region_name":"7","id":"rs1799316560","clinical_significance":[]},{"id":"rs1016132115","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140597193,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597193,"source":"dbSNP"},{"seq_region_name":"7","id":"rs534610397","clinical_significance":[],"strand":1,"feature_type":"variation","end":140597194,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597194,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1282788361","clinical_significance":[],"start":140597202,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140597202,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140597203,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597203,"clinical_significance":[],"seq_region_name":"7","id":"rs1799317053"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597204,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140597204,"clinical_significance":[],"seq_region_name":"7","id":"rs1299197134"},{"strand":1,"feature_type":"variation","end":140597206,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597206,"source":"dbSNP","seq_region_name":"7","id":"rs1585723237","clinical_significance":[]},{"seq_region_name":"7","id":"rs965224170","clinical_significance":[],"start":140597207,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140597207,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1799317506","clinical_significance":[],"end":140597208,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140597208,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["AAG","-"],"end":140597211,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597209,"clinical_significance":[],"seq_region_name":"7","id":"rs1799317600"},{"id":"rs975765305","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140597214,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597214,"source":"dbSNP"},{"clinical_significance":[],"id":"rs769111352","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597222,"feature_type":"variation","strand":1,"end":140597222,"alleles":["A","C"]},{"feature_type":"variation","strand":1,"end":140597229,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597229,"clinical_significance":[],"seq_region_name":"7","id":"rs1799318011"},{"alleles":["A","C","G"],"end":140597231,"feature_type":"variation","strand":1,"source":"dbSNP","start":140597231,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs73500418","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140597232,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597232,"clinical_significance":[],"seq_region_name":"7","id":"rs1368388681"},{"seq_region_name":"7","id":"rs1799318464","clinical_significance":[],"alleles":["A","G"],"end":140597246,"strand":1,"feature_type":"variation","start":140597246,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1302185385","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597255,"source":"dbSNP","strand":1,"feature_type":"variation","end":140597255,"alleles":["C","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597260,"source":"dbSNP","strand":1,"feature_type":"variation","end":140597260,"alleles":["G","T"],"seq_region_name":"7","id":"rs993719011","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140597261,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597261,"clinical_significance":[],"seq_region_name":"7","id":"rs953544940"},{"alleles":["G","A"],"end":140597269,"strand":1,"feature_type":"variation","start":140597269,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799318868","clinical_significance":[]},{"start":140597275,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140597275,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","id":"rs990154914","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1316133299","clinical_significance":[],"strand":1,"feature_type":"variation","end":140597276,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597276,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140597279,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597279,"clinical_significance":[],"id":"rs1400113617","seq_region_name":"7"},{"seq_region_name":"7","id":"rs914544597","clinical_significance":[],"strand":1,"feature_type":"variation","end":140597284,"alleles":["T","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597284,"source":"dbSNP"},{"alleles":["C","A","T"],"end":140597290,"strand":1,"feature_type":"variation","start":140597290,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs577969803","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1487459204","source":"dbSNP","start":140597296,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","-"],"end":140597296,"feature_type":"variation","strand":1},{"start":140597298,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140597298,"alleles":["A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1175333975","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597306,"feature_type":"variation","strand":1,"end":140597306,"alleles":["A","C"],"clinical_significance":[],"id":"rs946129653","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799319896","clinical_significance":[],"start":140597309,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140597309,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs977482992","clinical_significance":[],"strand":1,"feature_type":"variation","end":140597315,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597315,"source":"dbSNP"},{"end":140597316,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140597316,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1394730306"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1187275247","source":"dbSNP","start":140597320,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140597320,"alleles":["C","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1799320325","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140597324,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597324,"source":"dbSNP"},{"source":"dbSNP","start":140597327,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140597327,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs189003258","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140597329,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597329,"source":"dbSNP","id":"rs938853153","seq_region_name":"7","clinical_significance":[]},{"end":140597331,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140597331,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1240499627","clinical_significance":[]},{"alleles":["G","A"],"end":140597334,"strand":1,"feature_type":"variation","start":140597334,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1799320783","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799320882","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597342,"feature_type":"variation","strand":1,"end":140597342,"alleles":["T","C"]},{"strand":1,"feature_type":"variation","end":140597344,"alleles":["TTT","TT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597342,"source":"dbSNP","seq_region_name":"7","id":"rs2130675815","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140597349,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597349,"source":"dbSNP","seq_region_name":"7","id":"rs1192549766","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597350,"source":"dbSNP","strand":1,"feature_type":"variation","end":140597350,"alleles":["C","T"],"seq_region_name":"7","id":"rs1799321105","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140597358,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597358,"source":"dbSNP","seq_region_name":"7","id":"rs1486315427","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597362,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140597362,"clinical_significance":[],"seq_region_name":"7","id":"rs1490802038"},{"strand":1,"feature_type":"variation","end":140597363,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597363,"source":"dbSNP","seq_region_name":"7","id":"rs986221580","clinical_significance":[]},{"alleles":["T","G"],"end":140597364,"strand":1,"feature_type":"variation","start":140597364,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1056489119","clinical_significance":[]},{"alleles":["C","T"],"end":140597366,"feature_type":"variation","strand":1,"source":"dbSNP","start":140597366,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs557165365"},{"alleles":["G","A","C","T"],"end":140597367,"strand":1,"feature_type":"variation","start":140597367,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs748512471","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597368,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140597368,"seq_region_name":"7","id":"rs1799321950","clinical_significance":[]},{"seq_region_name":"7","id":"rs1214720199","clinical_significance":[],"end":140597375,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140597375,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140597379,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140597379,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799322155","clinical_significance":[]},{"id":"rs575709306","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140597380,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597380,"source":"dbSNP"},{"start":140597384,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140597384,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585723526","clinical_significance":[]},{"seq_region_name":"7","id":"rs886752838","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597386,"source":"dbSNP","strand":1,"feature_type":"variation","end":140597386,"alleles":["C","G","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597387,"feature_type":"variation","strand":1,"end":140597387,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1267957568"},{"seq_region_name":"7","id":"rs1429386015","clinical_significance":[],"end":140597394,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140597394,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597396,"feature_type":"variation","strand":1,"end":140597396,"alleles":["T","C","G"],"clinical_significance":[],"id":"rs989513335","seq_region_name":"7"},{"end":140597399,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140597399,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1412717034","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140597409,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597409,"source":"dbSNP","seq_region_name":"7","id":"rs1003942193","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799323165","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597411,"source":"dbSNP","strand":1,"feature_type":"variation","end":140597411,"alleles":["G","A"]},{"alleles":["A","C","G"],"end":140597418,"strand":1,"feature_type":"variation","start":140597418,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs914129391","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140597419,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597419,"clinical_significance":[],"seq_region_name":"7","id":"rs1378070959"},{"alleles":["A","G"],"end":140597421,"feature_type":"variation","strand":1,"source":"dbSNP","start":140597421,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs542789545"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1417615083","alleles":["G","A"],"end":140597424,"feature_type":"variation","strand":1,"source":"dbSNP","start":140597424,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1167452338","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597425,"source":"dbSNP","strand":1,"feature_type":"variation","end":140597425,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799323864","feature_type":"variation","strand":1,"end":140597427,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597427},{"source":"dbSNP","start":140597429,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C","G"],"end":140597429,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs139975390"},{"start":140597434,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140597434,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs1799323974","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799324092","clinical_significance":[],"start":140597436,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140597442,"alleles":["TTTTTTT","TTTTTT"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799324212","end":140597441,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140597441,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799324307","feature_type":"variation","strand":1,"end":140597444,"alleles":["AA","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597443},{"end":140597445,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140597445,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1799324417","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1186352114","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597453,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140597453},{"clinical_significance":[],"seq_region_name":"7","id":"rs928169764","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597456,"feature_type":"variation","strand":1,"end":140597456,"alleles":["G","T"]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140597459,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597459,"clinical_significance":[],"seq_region_name":"7","id":"rs1799324753"},{"end":140597460,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140597460,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1485549903"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1656207157","source":"dbSNP","start":140597462,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140597462,"alleles":["C","T"],"feature_type":"variation","strand":1},{"start":140597466,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140597466,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs901036588","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1233883002","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597467,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140597467},{"clinical_significance":[],"id":"rs996690243","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140597469,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597469},{"seq_region_name":"7","id":"rs1563167676","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597471,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140597471},{"id":"rs1366586120","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597482,"source":"dbSNP","strand":1,"feature_type":"variation","end":140597482,"alleles":["T","C"]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140597483,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597483,"source":"dbSNP","seq_region_name":"7","id":"rs1055473498","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140597484,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597484,"clinical_significance":[],"seq_region_name":"7","id":"rs1270408896"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597485,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140597485,"seq_region_name":"7","id":"rs1799325810","clinical_significance":[]},{"start":140597486,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140597486,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs1799325919","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140597487,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597487,"clinical_significance":[],"seq_region_name":"7","id":"rs1217514126"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799326128","source":"dbSNP","start":140597489,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140597492,"alleles":["TTTT","TTT"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1585723773","clinical_significance":[],"start":140597490,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140597490,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597492,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140597492,"seq_region_name":"7","id":"rs573202854","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597506,"feature_type":"variation","strand":1,"end":140597506,"alleles":["A","C"],"clinical_significance":[],"id":"rs894269391","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140597507,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597507,"source":"dbSNP","seq_region_name":"7","id":"rs1585723797","clinical_significance":[]},{"alleles":["C","T"],"end":140597508,"feature_type":"variation","strand":1,"source":"dbSNP","start":140597508,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130676167"},{"seq_region_name":"7","id":"rs1334860179","clinical_significance":[],"start":140597509,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140597509,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1799326906","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597514,"source":"dbSNP","strand":1,"feature_type":"variation","end":140597514,"alleles":["G","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597521,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140597521,"id":"rs1799327102","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs545050272","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140597529,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597529,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1412929849","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597530,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140597530},{"seq_region_name":"7","id":"rs1799327626","clinical_significance":[],"strand":1,"feature_type":"variation","end":140597532,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597532,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799327779","end":140597533,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140597533,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs957990920","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140597539,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597539},{"alleles":["A","C"],"end":140597541,"feature_type":"variation","strand":1,"source":"dbSNP","start":140597541,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130676221"},{"seq_region_name":"7","id":"rs540222809","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597544,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140597544},{"start":140597546,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140597546,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1367567109","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799328442","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597547,"feature_type":"variation","strand":1,"end":140597547,"alleles":["T","C"]},{"end":140597549,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140597549,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799328612","clinical_significance":[]},{"source":"dbSNP","start":140597552,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140597552,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799328781","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140597553,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597553,"clinical_significance":[],"seq_region_name":"7","id":"rs1799328963"},{"source":"dbSNP","start":140597557,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140597557,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799329146","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1353012009","end":140597559,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140597559,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140597560,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140597560,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1328384434"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1462041062","source":"dbSNP","start":140597563,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140597563,"alleles":["G","A"],"feature_type":"variation","strand":1},{"start":140597574,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140597577,"alleles":["TCTT","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799329900","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799330075","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597576,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140597576},{"id":"rs193040792","seq_region_name":"7","clinical_significance":[],"end":140597579,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140597579,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs2130676299","clinical_significance":[],"strand":1,"feature_type":"variation","end":140597583,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597583,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130676308","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597586,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140597586},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140597587,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597587,"source":"dbSNP","id":"rs1162867972","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1311634535","seq_region_name":"7","end":140597590,"alleles":["AA","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140597589,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs184753622","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140597593,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597593,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597595,"feature_type":"variation","strand":1,"end":140597595,"alleles":["C","A"],"clinical_significance":[],"id":"rs1799330739","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597599,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140597599,"seq_region_name":"7","id":"rs967356821","clinical_significance":[]},{"source":"dbSNP","start":140597602,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TGTTT","TGTTTGTTT"],"end":140597606,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1239704355"},{"id":"rs1007436888","seq_region_name":"7","clinical_significance":[],"alleles":["G","C"],"end":140597603,"strand":1,"feature_type":"variation","start":140597603,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140597604,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140597604,"strand":1,"feature_type":"variation","id":"rs2130676356","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1292161925","feature_type":"variation","strand":1,"end":140597605,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597605},{"id":"rs1197546256","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597611,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140597611},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597617,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140597617,"clinical_significance":[],"seq_region_name":"7","id":"rs1799331649"},{"clinical_significance":[],"id":"rs1799331816","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597618,"feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140597618},{"source":"dbSNP","start":140597619,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140597619,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1017691512","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs977535046","source":"dbSNP","start":140597622,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140597622,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799332397","source":"dbSNP","start":140597625,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140597625,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1799332610","clinical_significance":[],"end":140597627,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140597627,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140597628,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597628,"source":"dbSNP","seq_region_name":"7","id":"rs1230902373","clinical_significance":[]},{"clinical_significance":[],"id":"rs550781700","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140597635,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597635},{"clinical_significance":[],"id":"rs960358801","seq_region_name":"7","source":"dbSNP","start":140597636,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140597636,"alleles":["G","A"],"feature_type":"variation","strand":1},{"alleles":["A","G"],"end":140597640,"strand":1,"feature_type":"variation","start":140597640,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799333298","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140597641,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597641,"source":"dbSNP","seq_region_name":"7","id":"rs1799333477","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs560094499","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597644,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140597644},{"strand":1,"feature_type":"variation","end":140597648,"alleles":["TT","TTT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597647,"source":"dbSNP","seq_region_name":"7","id":"rs1799333847","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1225280870","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140597653,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597653},{"source":"dbSNP","start":140597657,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140597657,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799334202"},{"alleles":["G","A","T"],"end":140597660,"feature_type":"variation","strand":1,"source":"dbSNP","start":140597660,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs967337490"},{"seq_region_name":"7","id":"rs1308805432","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597662,"source":"dbSNP","strand":1,"feature_type":"variation","end":140597662,"alleles":["T","C"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597663,"feature_type":"variation","strand":1,"end":140597663,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs186485669"},{"source":"dbSNP","start":140597664,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140597664,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1441996702"},{"seq_region_name":"7","id":"rs1178415742","clinical_significance":[],"alleles":["G","T"],"end":140597666,"strand":1,"feature_type":"variation","start":140597666,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs765901979","source":"dbSNP","start":140597676,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140597676,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140597677,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140597677,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799335506"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597679,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140597679,"clinical_significance":[],"id":"rs1457443569","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597679,"feature_type":"variation","strand":1,"alleles":["CCCC","CCCCC"],"end":140597682,"clinical_significance":[],"seq_region_name":"7","id":"rs34207386"},{"start":140597687,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140597687,"strand":1,"feature_type":"variation","id":"rs1799336006","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1346336880","source":"dbSNP","start":140597692,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140597692,"feature_type":"variation","strand":1},{"alleles":["G","A"],"end":140597693,"feature_type":"variation","strand":1,"source":"dbSNP","start":140597693,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs142253160"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597695,"source":"dbSNP","strand":1,"feature_type":"variation","end":140597695,"alleles":["C","T"],"seq_region_name":"7","id":"rs959530742","clinical_significance":[]},{"clinical_significance":[],"id":"rs1407801667","seq_region_name":"7","alleles":["C","G","T"],"end":140597698,"feature_type":"variation","strand":1,"source":"dbSNP","start":140597698,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140597706,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140597706,"alleles":["T","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799337011","clinical_significance":[]},{"clinical_significance":[],"id":"rs2130676557","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","T"],"end":140597708,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597708},{"id":"rs916034646","seq_region_name":"7","clinical_significance":[],"alleles":["G","C"],"end":140597713,"strand":1,"feature_type":"variation","start":140597713,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1454481852","end":140597714,"alleles":["A","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140597714,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1254461241","clinical_significance":[],"start":140597716,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","-"],"end":140597716,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597717,"source":"dbSNP","strand":1,"feature_type":"variation","end":140597717,"alleles":["A","C"],"seq_region_name":"7","id":"rs1211318712","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799338011","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597719,"source":"dbSNP","strand":1,"feature_type":"variation","end":140597719,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1487846868","clinical_significance":[],"end":140597721,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140597721,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs548853518","clinical_significance":[],"alleles":["G","A"],"end":140597727,"strand":1,"feature_type":"variation","start":140597727,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs2130676596","clinical_significance":[],"strand":1,"feature_type":"variation","end":140597730,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597730,"source":"dbSNP"},{"alleles":["T","C"],"end":140597738,"strand":1,"feature_type":"variation","start":140597738,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs151259271","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1407468369","feature_type":"variation","strand":1,"end":140597739,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597739},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140597742,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597742,"clinical_significance":[],"seq_region_name":"7","id":"rs908245634"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597745,"feature_type":"variation","strand":1,"end":140597745,"alleles":["G","T"],"clinical_significance":[],"id":"rs1163180627","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799339008","clinical_significance":[],"start":140597752,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140597752,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1234717066","clinical_significance":[],"end":140597753,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140597753,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140597754,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597754,"source":"dbSNP","seq_region_name":"7","id":"rs1349797481","clinical_significance":[]},{"alleles":["G","C"],"end":140597755,"feature_type":"variation","strand":1,"source":"dbSNP","start":140597755,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1373516133"},{"start":140597757,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140597757,"alleles":["G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799339458","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140597760,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597760,"source":"dbSNP","seq_region_name":"7","id":"rs191286130","clinical_significance":[]},{"seq_region_name":"7","id":"rs1333372377","clinical_significance":[],"start":140597761,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140597761,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs2130676705","clinical_significance":[],"end":140597762,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140597762,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799339800","feature_type":"variation","strand":1,"end":140597763,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597763},{"end":140597764,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140597764,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799339915","clinical_significance":[]},{"start":140597767,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140597767,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs774636514","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585724350","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597768,"feature_type":"variation","strand":1,"end":140597768,"alleles":["T","C"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597769,"source":"dbSNP","strand":1,"feature_type":"variation","end":140597769,"alleles":["T","C"],"id":"rs900925114","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140597776,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140597776,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799340341"},{"seq_region_name":"7","id":"rs1452330162","clinical_significance":[],"strand":1,"feature_type":"variation","end":140597779,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597779,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799340572","end":140597780,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140597780,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1446264264","source":"dbSNP","start":140597781,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140597781,"alleles":["C","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1360425901","clinical_significance":[],"alleles":["A","C"],"end":140597785,"strand":1,"feature_type":"variation","start":140597785,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597787,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140597787,"id":"rs2130676797","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1174703185","seq_region_name":"7","alleles":["G","A"],"end":140597789,"feature_type":"variation","strand":1,"source":"dbSNP","start":140597789,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs996968305","end":140597790,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140597790,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597791,"source":"dbSNP","strand":1,"feature_type":"variation","end":140597791,"alleles":["G","A"],"seq_region_name":"7","id":"rs140497273","clinical_significance":[]},{"id":"rs1799341210","seq_region_name":"7","clinical_significance":[],"start":140597797,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140597797,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799341328","alleles":["C","A"],"end":140597803,"feature_type":"variation","strand":1,"source":"dbSNP","start":140597803,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1191304315","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597804,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140597804},{"clinical_significance":[],"seq_region_name":"7","id":"rs1226372895","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597805,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140597805},{"clinical_significance":[],"seq_region_name":"7","id":"rs1432092093","alleles":["G","T"],"end":140597808,"feature_type":"variation","strand":1,"source":"dbSNP","start":140597808,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs893622290","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597809,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140597809},{"clinical_significance":[],"seq_region_name":"7","id":"rs1010855287","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597810,"feature_type":"variation","strand":1,"end":140597810,"alleles":["A","G"]},{"start":140597816,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140597816,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","id":"rs779003779","seq_region_name":"7","clinical_significance":[]},{"id":"rs571589020","seq_region_name":"7","clinical_significance":[],"alleles":["C","G","T"],"end":140597820,"strand":1,"feature_type":"variation","start":140597820,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597821,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140597821,"clinical_significance":[],"seq_region_name":"7","id":"rs893874138"},{"clinical_significance":[],"id":"rs967408757","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597829,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140597829},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597833,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140597833,"id":"rs1799342527","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799342662","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597841,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140597841},{"clinical_significance":[],"id":"rs1799342779","seq_region_name":"7","source":"dbSNP","start":140597843,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140597843,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1255536999","clinical_significance":[],"start":140597844,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140597844,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs998857478","alleles":["C","G","T"],"end":140597845,"feature_type":"variation","strand":1,"source":"dbSNP","start":140597845,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["C","A","G","T"],"end":140597847,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597847,"source":"dbSNP","seq_region_name":"7","id":"rs1349724158","clinical_significance":[]},{"end":140597848,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140597848,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs548888066","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799343511","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140597855,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597855,"source":"dbSNP"},{"id":"rs1036065733","seq_region_name":"7","clinical_significance":[],"start":140597856,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140597856,"alleles":["G","A","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799343770","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597861,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140597861},{"end":140597867,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140597867,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1799343887","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597868,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140597868,"clinical_significance":[],"seq_region_name":"7","id":"rs1799344025"},{"clinical_significance":[],"seq_region_name":"7","id":"rs538901639","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597871,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140597871},{"source":"dbSNP","start":140597874,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140597874,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1011010720","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1585724582","clinical_significance":[],"alleles":["A","G"],"end":140597875,"strand":1,"feature_type":"variation","start":140597875,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1380574787","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140597885,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597885},{"strand":1,"feature_type":"variation","end":140597889,"alleles":["A","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597889,"source":"dbSNP","seq_region_name":"7","id":"rs960162885","clinical_significance":[]},{"id":"rs991959097","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140597891,"strand":1,"feature_type":"variation","start":140597891,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597892,"feature_type":"variation","strand":1,"end":140597892,"alleles":["G","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1180477406"},{"strand":1,"feature_type":"variation","end":140597896,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597896,"source":"dbSNP","seq_region_name":"7","id":"rs1413533617","clinical_significance":[]},{"end":140597897,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140597897,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799345063","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140597901,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597901,"source":"dbSNP","seq_region_name":"7","id":"rs1799345179","clinical_significance":[]},{"source":"dbSNP","start":140597907,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140597907,"alleles":["T","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1410964996","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799345402","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140597913,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597913,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597919,"feature_type":"variation","strand":1,"end":140597919,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130677061"},{"end":140597925,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140597925,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1003993237","clinical_significance":[]},{"seq_region_name":"7","id":"rs557277669","clinical_significance":[],"strand":1,"feature_type":"variation","end":140597927,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597927,"source":"dbSNP"},{"alleles":["G","C"],"end":140597931,"feature_type":"variation","strand":1,"source":"dbSNP","start":140597931,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799345723"},{"alleles":["C","G"],"end":140597932,"feature_type":"variation","strand":1,"source":"dbSNP","start":140597932,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1373265601","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597958,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140597958,"clinical_significance":[],"seq_region_name":"7","id":"rs1173487078"},{"end":140597967,"alleles":["A","C","T"],"strand":1,"feature_type":"variation","start":140597967,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs753635599","clinical_significance":[]},{"end":140597980,"alleles":["-","A"],"strand":1,"feature_type":"variation","start":140597981,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799346230","clinical_significance":[]},{"start":140597981,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140597981,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1262411923","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140597984,"alleles":["AAA","AA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597982,"source":"dbSNP","seq_region_name":"7","id":"rs1799346457","clinical_significance":[]},{"start":140597986,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140597986,"alleles":["A","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs916104541","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799346713","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140597987,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140597987},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597988,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140597988,"clinical_significance":[],"id":"rs1398157822","seq_region_name":"7"},{"start":140597989,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140597989,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs568985166","clinical_significance":[]},{"alleles":["-","AAAGATA"],"end":140597990,"feature_type":"variation","strand":1,"source":"dbSNP","start":140597991,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799347094"},{"seq_region_name":"7","id":"rs1799347208","clinical_significance":[],"start":140597992,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140597992,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140597995,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597995,"clinical_significance":[],"id":"rs1799347325","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799347424","feature_type":"variation","strand":1,"alleles":["-","GAAATAAAAGAGGATACAAA"],"end":140597995,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140597996},{"seq_region_name":"7","id":"rs1799347532","clinical_significance":[],"alleles":["C","G"],"end":140597996,"strand":1,"feature_type":"variation","start":140597996,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140597998,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140597998,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799347644","clinical_significance":[]},{"alleles":["-","ACAAA"],"end":140597998,"strand":1,"feature_type":"variation","start":140597999,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799347754","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799347859","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598002,"source":"dbSNP","strand":1,"feature_type":"variation","end":140598002,"alleles":["G","C","T"]},{"feature_type":"variation","strand":1,"end":140598005,"alleles":["T","C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598005,"clinical_significance":[],"id":"rs1337522526","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1342469198","source":"dbSNP","start":140598006,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140598006,"alleles":["G","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1446172337","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598007,"source":"dbSNP","strand":1,"feature_type":"variation","end":140598007,"alleles":["T","A"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598012,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140598012,"clinical_significance":[],"seq_region_name":"7","id":"rs536443134"},{"clinical_significance":[],"id":"rs1799348490","seq_region_name":"7","end":140598013,"alleles":["-","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140598014,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140598014,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140598014,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799348600"},{"id":"rs1799348713","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140598016,"alleles":["AA","AATAAAAA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598015,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs34739119","alleles":["AAAAAAAA","AAAAAAA","AAAAAAAAA","AAAAAAAAAA"],"end":140598022,"feature_type":"variation","strand":1,"source":"dbSNP","start":140598015,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799349061","source":"dbSNP","start":140598018,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140598018,"alleles":["A","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1799349165","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140598021,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598021,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598024,"source":"dbSNP","strand":1,"feature_type":"variation","end":140598024,"alleles":["A","G","T"],"seq_region_name":"7","id":"rs1340372760","clinical_significance":[]},{"alleles":["A","AA"],"end":140598024,"strand":1,"feature_type":"variation","start":140598024,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1799349413","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799349529","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598028,"source":"dbSNP","strand":1,"feature_type":"variation","end":140598028,"alleles":["T","C"]},{"strand":1,"feature_type":"variation","alleles":["TGCAATAAAACCCAAGTCTAGACCAGTCTAATTTATTTACTGAT","T"],"end":140598071,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598028,"source":"dbSNP","seq_region_name":"7","id":"rs1799349624","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140598030,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598030,"source":"dbSNP","seq_region_name":"7","id":"rs1799349750","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140598031,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598031,"source":"dbSNP","id":"rs1799349869","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140598035,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140598035,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130677338"},{"alleles":["A","T"],"end":140598036,"feature_type":"variation","strand":1,"source":"dbSNP","start":140598036,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799349987"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598038,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140598038,"clinical_significance":[],"seq_region_name":"7","id":"rs1362414759"},{"source":"dbSNP","start":140598041,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AA","-"],"end":140598042,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1220336182"},{"seq_region_name":"7","id":"rs1317314497","clinical_significance":[],"end":140598050,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140598050,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1294454127","clinical_significance":[],"strand":1,"feature_type":"variation","end":140598055,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598055,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1235744854","clinical_significance":[],"strand":1,"feature_type":"variation","end":140598062,"alleles":["TAATTTA","TA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598056,"source":"dbSNP"},{"start":140598060,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A","G"],"end":140598060,"strand":1,"feature_type":"variation","id":"rs183976079","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140598063,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140598063,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1354096507"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799350896","source":"dbSNP","start":140598071,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140598071,"alleles":["T","C"],"feature_type":"variation","strand":1},{"alleles":["C","-"],"end":140598073,"feature_type":"variation","strand":1,"source":"dbSNP","start":140598073,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1333976654","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799351010","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598073,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140598073},{"seq_region_name":"7","id":"rs2130677403","clinical_significance":[],"strand":1,"feature_type":"variation","end":140598078,"alleles":["AAAAA","AAAA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598074,"source":"dbSNP"},{"start":140598079,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140598079,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1306426721","clinical_significance":[]},{"clinical_significance":[],"id":"rs1392296656","seq_region_name":"7","source":"dbSNP","start":140598085,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140598085,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1396803189","seq_region_name":"7","feature_type":"variation","strand":1,"end":140598092,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598092},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799351530","source":"dbSNP","start":140598098,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140598101,"alleles":["AAAA","AAA"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs368519550","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598101,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140598101},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598106,"source":"dbSNP","strand":1,"feature_type":"variation","end":140598106,"alleles":["G","C"],"seq_region_name":"7","id":"rs1299475075","clinical_significance":[]},{"start":140598110,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140598110,"strand":1,"feature_type":"variation","id":"rs959644787","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140598111,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140598111,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1422201393"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1164993727","alleles":["C","T"],"end":140598112,"feature_type":"variation","strand":1,"source":"dbSNP","start":140598112,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1799352355","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140598113,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598113,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1799352459","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598114,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140598114},{"source":"dbSNP","start":140598120,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140598120,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799352554"},{"seq_region_name":"7","id":"rs1799352682","clinical_significance":[],"end":140598123,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140598123,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs908797560","end":140598125,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140598125,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1317261755","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598126,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140598126},{"seq_region_name":"7","id":"rs1799353072","clinical_significance":[],"end":140598129,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140598129,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1799353183","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140598130,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598130,"source":"dbSNP"},{"seq_region_name":"7","id":"rs2130677525","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140598131,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598131,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs761474234","source":"dbSNP","start":140598137,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140598137,"alleles":["C","T"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598138,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140598138,"clinical_significance":[],"seq_region_name":"7","id":"rs910065322"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598144,"source":"dbSNP","strand":1,"feature_type":"variation","end":140598144,"alleles":["G","A"],"seq_region_name":"7","id":"rs1252948396","clinical_significance":[]},{"seq_region_name":"7","id":"rs1040725831","clinical_significance":[],"alleles":["T","C"],"end":140598151,"strand":1,"feature_type":"variation","start":140598151,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["CCCCC","CCCCCC"],"end":140598156,"feature_type":"variation","strand":1,"source":"dbSNP","start":140598152,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1196914739"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799353835","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598159,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140598159},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140598163,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598163,"clinical_significance":[],"seq_region_name":"7","id":"rs1799353950"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799354066","feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140598166,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598166},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598169,"feature_type":"variation","strand":1,"end":140598169,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130677586"},{"seq_region_name":"7","id":"rs922234677","clinical_significance":[],"strand":1,"feature_type":"variation","end":140598170,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598170,"source":"dbSNP"},{"end":140598175,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140598175,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799354294","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799354402","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140598176,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598176,"source":"dbSNP"},{"id":"rs1799354514","seq_region_name":"7","clinical_significance":[],"end":140598179,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140598179,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140598189,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598189,"clinical_significance":[],"id":"rs1457484142","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1273951670","source":"dbSNP","start":140598192,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140598192,"alleles":["C","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1585725047","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598193,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140598193},{"seq_region_name":"7","id":"rs1215607737","clinical_significance":[],"start":140598194,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C","G"],"end":140598194,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1799355036","clinical_significance":[],"start":140598195,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140598195,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"alleles":["A","G"],"end":140598196,"feature_type":"variation","strand":1,"source":"dbSNP","start":140598196,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799355141"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598208,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140598208,"seq_region_name":"7","id":"rs1799355249","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1333385727","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140598216,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598216},{"seq_region_name":"7","id":"rs1799355452","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140598217,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598217,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598220,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140598220,"seq_region_name":"7","id":"rs1284080979","clinical_significance":[]},{"clinical_significance":[],"id":"rs1203738378","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598221,"feature_type":"variation","strand":1,"alleles":["ATAT","AT"],"end":140598224},{"id":"rs1799355766","seq_region_name":"7","clinical_significance":[],"alleles":["T","A"],"end":140598224,"strand":1,"feature_type":"variation","start":140598224,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140598232,"alleles":["ATCATCA","ATCA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598226,"clinical_significance":[],"id":"rs1337842461","seq_region_name":"7"},{"source":"dbSNP","start":140598227,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140598227,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs932439883"},{"end":140598229,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140598229,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs372090282"},{"source":"dbSNP","start":140598233,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140598233,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130677720"},{"alleles":["C","G"],"end":140598240,"feature_type":"variation","strand":1,"source":"dbSNP","start":140598240,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs765101987"},{"clinical_significance":[],"seq_region_name":"7","id":"rs531497474","source":"dbSNP","start":140598246,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C","T"],"end":140598246,"feature_type":"variation","strand":1},{"start":140598253,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140598253,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799356474","clinical_significance":[]},{"seq_region_name":"7","id":"rs1326044587","clinical_significance":[],"start":140598256,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","-"],"end":140598256,"strand":1,"feature_type":"variation"},{"end":140598257,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140598257,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1462523735"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1388522476","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598259,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140598259},{"seq_region_name":"7","id":"rs1209007163","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598267,"source":"dbSNP","strand":1,"feature_type":"variation","end":140598267,"alleles":["T","A"]},{"strand":1,"feature_type":"variation","end":140598268,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598268,"source":"dbSNP","seq_region_name":"7","id":"rs1799356966","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["TCTAGTC","TC"],"end":140598275,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598269,"clinical_significance":[],"seq_region_name":"7","id":"rs202172230"},{"feature_type":"variation","strand":1,"end":140598278,"alleles":["CTAGTCCTA","CTA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598270,"clinical_significance":[],"id":"rs139345636","seq_region_name":"7"},{"source":"dbSNP","start":140598273,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140598273,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799357305","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585725190","source":"dbSNP","start":140598275,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140598275,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1475965694","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598277,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140598277},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598279,"source":"dbSNP","strand":1,"feature_type":"variation","end":140598279,"alleles":["A","G"],"id":"rs1470394567","seq_region_name":"7","clinical_significance":[]},{"id":"rs554804548","seq_region_name":"7","clinical_significance":[],"start":140598283,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140598283,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140598288,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598288,"source":"dbSNP","seq_region_name":"7","id":"rs1585725233","clinical_significance":[]},{"seq_region_name":"7","id":"rs1051894318","clinical_significance":[],"alleles":["C","T"],"end":140598289,"strand":1,"feature_type":"variation","start":140598289,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1176526936","seq_region_name":"7","feature_type":"variation","strand":1,"end":140598291,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598291},{"clinical_significance":[],"seq_region_name":"7","id":"rs911791493","end":140598293,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140598293,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs943288537","seq_region_name":"7","source":"dbSNP","start":140598295,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140598295,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1799358381","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598309,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140598309},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799358481","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598312,"feature_type":"variation","strand":1,"end":140598312,"alleles":["A","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1422086365","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140598314,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598314},{"seq_region_name":"7","id":"rs1449885739","clinical_significance":[],"end":140598318,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140598318,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140598320,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140598320,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799358808","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799358912","source":"dbSNP","start":140598321,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140598321,"alleles":["T","C"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598323,"source":"dbSNP","strand":1,"feature_type":"variation","end":140598323,"alleles":["A","T"],"id":"rs574079026","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs902438777","feature_type":"variation","strand":1,"end":140598325,"alleles":["T","C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598325},{"feature_type":"variation","strand":1,"end":140598327,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598327,"clinical_significance":[],"id":"rs1003841134","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1035712902","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598328,"feature_type":"variation","strand":1,"end":140598328,"alleles":["A","G","T"]},{"source":"dbSNP","start":140598331,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140598331,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799359450"},{"clinical_significance":[],"seq_region_name":"7","id":"rs895787598","feature_type":"variation","strand":1,"end":140598332,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598332},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598337,"source":"dbSNP","strand":1,"feature_type":"variation","end":140598337,"alleles":["A","G"],"seq_region_name":"7","id":"rs1585725387","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1038860332","end":140598339,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140598339,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799359902","source":"dbSNP","start":140598340,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140598340,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1259388792","clinical_significance":[],"strand":1,"feature_type":"variation","end":140598346,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598346,"source":"dbSNP"},{"seq_region_name":"7","id":"rs893653362","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598359,"source":"dbSNP","strand":1,"feature_type":"variation","end":140598359,"alleles":["C","A"]},{"alleles":["CTGT","CTGTCTGT"],"end":140598363,"feature_type":"variation","strand":1,"source":"dbSNP","start":140598360,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799360241"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598361,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140598361,"clinical_significance":[],"id":"rs1799360355","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598366,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140598366,"clinical_significance":[],"seq_region_name":"7","id":"rs1013032106"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1303626633","end":140598367,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140598367,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140598368,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140598368,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs150437870","clinical_significance":[]},{"end":140598372,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140598372,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799360823","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140598375,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598375,"clinical_significance":[],"id":"rs1328784999","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799361035","clinical_significance":[],"start":140598376,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140598376,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1799361148","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","GG"],"end":140598380,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598380,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs549802930","feature_type":"variation","strand":1,"end":140598381,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598381},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598382,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140598382,"seq_region_name":"7","id":"rs558491526","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799361573","clinical_significance":[],"end":140598386,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140598386,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs902631887","seq_region_name":"7","end":140598387,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140598387,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140598389,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140598390,"alleles":["TT","TTT"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1333779311"},{"alleles":["T","C"],"end":140598396,"feature_type":"variation","strand":1,"source":"dbSNP","start":140598396,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1015683093"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598399,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140598399,"clinical_significance":[],"seq_region_name":"7","id":"rs1395942353"},{"strand":1,"feature_type":"variation","end":140598400,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598400,"source":"dbSNP","seq_region_name":"7","id":"rs1195666543","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598402,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140598402,"clinical_significance":[],"seq_region_name":"7","id":"rs57916123"},{"clinical_significance":[],"id":"rs544534947","seq_region_name":"7","alleles":["G","A"],"end":140598403,"feature_type":"variation","strand":1,"source":"dbSNP","start":140598403,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs147697027","seq_region_name":"7","clinical_significance":[],"start":140598406,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140598406,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140598407,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598407,"clinical_significance":[],"seq_region_name":"7","id":"rs1799362555"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1339754155","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598408,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140598408},{"seq_region_name":"7","id":"rs1799362767","clinical_significance":[],"end":140598410,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140598410,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140598413,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140598413,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1012460117","clinical_significance":[]},{"start":140598415,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140598415,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130678123","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs189749373","feature_type":"variation","strand":1,"end":140598417,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598417},{"id":"rs1216374281","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140598418,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598418,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598421,"source":"dbSNP","strand":1,"feature_type":"variation","end":140598421,"alleles":["G","A"],"seq_region_name":"7","id":"rs1348979918","clinical_significance":[]},{"alleles":["T","C"],"end":140598423,"strand":1,"feature_type":"variation","start":140598423,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1280607225","clinical_significance":[]},{"seq_region_name":"7","id":"rs1220666938","clinical_significance":[],"alleles":["C","T"],"end":140598426,"strand":1,"feature_type":"variation","start":140598426,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140598430,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140598430,"alleles":["A","-"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1563168150","clinical_significance":[]},{"source":"dbSNP","start":140598432,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140598432,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1342424829"},{"clinical_significance":[],"seq_region_name":"7","id":"rs142506572","feature_type":"variation","strand":1,"end":140598434,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598434},{"seq_region_name":"7","id":"rs985264754","clinical_significance":[],"alleles":["G","A"],"end":140598435,"strand":1,"feature_type":"variation","start":140598435,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140598438,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598438,"source":"dbSNP","seq_region_name":"7","id":"rs2130678186","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598442,"source":"dbSNP","strand":1,"feature_type":"variation","end":140598442,"alleles":["C","T"],"seq_region_name":"7","id":"rs2130678197","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1026049289","feature_type":"variation","strand":1,"end":140598449,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598449},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140598450,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598450,"clinical_significance":[],"seq_region_name":"7","id":"rs1296212263"},{"clinical_significance":[],"seq_region_name":"7","id":"rs560825288","source":"dbSNP","start":140598451,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140598451,"alleles":["G","A","C","T"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140598455,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140598455,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1563168172","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs879154151","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598462,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140598462},{"seq_region_name":"7","id":"rs1799364521","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","-"],"end":140598467,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598467,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598473,"feature_type":"variation","strand":1,"end":140598473,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs987134163"},{"end":140598474,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140598474,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799364762"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1424688827","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140598478,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598478},{"seq_region_name":"7","id":"rs1168601931","clinical_significance":[],"end":140598479,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140598479,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1799365139","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140598490,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598490,"source":"dbSNP"},{"seq_region_name":"7","id":"rs946413835","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598496,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140598496},{"feature_type":"variation","strand":1,"end":140598498,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598498,"clinical_significance":[],"seq_region_name":"7","id":"rs1042257820"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598501,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","-"],"end":140598501,"id":"rs752662802","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","C"],"end":140598505,"feature_type":"variation","strand":1,"source":"dbSNP","start":140598505,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799365557"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598512,"feature_type":"variation","strand":1,"alleles":["ATGATGAT","ATGAT"],"end":140598519,"clinical_significance":[],"id":"rs1284486738","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799365788","source":"dbSNP","start":140598514,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140598514,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799365953","feature_type":"variation","strand":1,"end":140598515,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598515},{"alleles":["T","C"],"end":140598519,"feature_type":"variation","strand":1,"source":"dbSNP","start":140598519,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130678323"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1422129219","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598525,"feature_type":"variation","strand":1,"end":140598525,"alleles":["G","A"]},{"source":"dbSNP","start":140598528,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140598528,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799366106"},{"start":140598534,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140598534,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs181773131","clinical_significance":[]},{"id":"rs939306575","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140598535,"strand":1,"feature_type":"variation","start":140598535,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799366496","feature_type":"variation","strand":1,"alleles":["TATAT","TAT"],"end":140598543,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598539},{"feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140598541,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598541,"clinical_significance":[],"seq_region_name":"7","id":"rs974661796"},{"start":140598542,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140598542,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1056772835","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140598543,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598543,"clinical_significance":[],"seq_region_name":"7","id":"rs1440372257"},{"end":140598547,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140598547,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs546634215","clinical_significance":[]},{"start":140598549,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140598549,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1488210268","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130678381","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598550,"feature_type":"variation","strand":1,"end":140598550,"alleles":["T","A"]},{"id":"rs2130678387","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140598551,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598551,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs895850784","alleles":["T","C"],"end":140598552,"feature_type":"variation","strand":1,"source":"dbSNP","start":140598552,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1214665578","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598553,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140598553},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598554,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140598554,"clinical_significance":[],"seq_region_name":"7","id":"rs2130678408"},{"source":"dbSNP","start":140598556,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140598556,"alleles":["T","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799367398"},{"clinical_significance":[],"id":"rs1013331545","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140598559,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598559},{"id":"rs1799367617","seq_region_name":"7","clinical_significance":[],"start":140598566,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140598569,"alleles":["AACA","-"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1200214484","clinical_significance":[],"end":140598571,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140598571,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140598573,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598573,"clinical_significance":[],"seq_region_name":"7","id":"rs1563168237"},{"seq_region_name":"7","id":"rs1022882962","clinical_significance":[],"strand":1,"feature_type":"variation","end":140598574,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598574,"source":"dbSNP"},{"source":"dbSNP","start":140598575,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140598575,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1276230347","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799368182","end":140598581,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140598581,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1709458670","source":"dbSNP","start":140598584,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140598584,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598589,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140598589,"clinical_significance":[],"seq_region_name":"7","id":"rs1563168240"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598592,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140598592,"clinical_significance":[],"seq_region_name":"7","id":"rs571297688"},{"source":"dbSNP","start":140598599,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140598599,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799368524","seq_region_name":"7"},{"seq_region_name":"7","id":"rs2130678502","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140598602,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598602,"source":"dbSNP"},{"end":140598605,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140598605,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585725951","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598605,"feature_type":"variation","strand":1,"end":140598610,"alleles":["AAAAAA","AAAAA"],"clinical_significance":[],"seq_region_name":"7","id":"rs202033629"},{"alleles":["A","T"],"end":140598610,"strand":1,"feature_type":"variation","start":140598610,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799368886","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799369004","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598613,"feature_type":"variation","strand":1,"end":140598613,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1445489185","alleles":["C","T"],"end":140598615,"feature_type":"variation","strand":1,"source":"dbSNP","start":140598615,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs545890127","feature_type":"variation","strand":1,"alleles":["ATATATATA","ATATATATATA"],"end":140598624,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598616},{"clinical_significance":[],"seq_region_name":"7","id":"rs1005566084","feature_type":"variation","strand":1,"end":140598617,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598617},{"seq_region_name":"7","id":"rs1799369425","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140598619,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598619,"source":"dbSNP"},{"seq_region_name":"7","id":"rs533199294","clinical_significance":[],"alleles":["A","C","G"],"end":140598620,"strand":1,"feature_type":"variation","start":140598620,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799369670","source":"dbSNP","start":140598623,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140598623,"alleles":["T","-"],"feature_type":"variation","strand":1},{"end":140598630,"alleles":["ACACACA","ACACACACA"],"strand":1,"feature_type":"variation","start":140598624,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799369778","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799369880","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598626,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140598626},{"seq_region_name":"7","id":"rs1329722340","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598628,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140598628},{"seq_region_name":"7","id":"rs1799370082","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598628,"source":"dbSNP","strand":1,"feature_type":"variation","end":140598634,"alleles":["ACAAACA","ACA"]},{"seq_region_name":"7","id":"rs1799370193","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","-"],"end":140598629,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598629,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130678629","end":140598630,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140598630,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1411737455","alleles":["C","T"],"end":140598633,"feature_type":"variation","strand":1,"source":"dbSNP","start":140598633,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140598634,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598634,"source":"dbSNP","id":"rs1799370375","seq_region_name":"7","clinical_significance":[]},{"id":"rs185279525","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140598635,"strand":1,"feature_type":"variation","start":140598635,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140598637,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140598637,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1170045992","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598637,"feature_type":"variation","strand":1,"end":140598637,"alleles":["C","-"],"clinical_significance":[],"seq_region_name":"7","id":"rs1788617865"},{"alleles":["C","A","T"],"end":140598639,"strand":1,"feature_type":"variation","start":140598639,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs569123470","clinical_significance":[]},{"source":"dbSNP","start":140598646,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140598646,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1012241198"},{"seq_region_name":"7","id":"rs1799370897","clinical_significance":[],"start":140598646,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AGAG","AG"],"end":140598649,"strand":1,"feature_type":"variation"},{"end":140598648,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140598648,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1472644549","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140598649,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598649,"source":"dbSNP","id":"rs1799371097","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799371200","clinical_significance":[],"start":140598650,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140598650,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1236545989","source":"dbSNP","start":140598654,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140598654,"alleles":["C","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799371426","source":"dbSNP","start":140598662,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140598662,"feature_type":"variation","strand":1},{"id":"rs374424714","seq_region_name":"7","clinical_significance":[],"start":140598666,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140598666,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["A","C","T"],"end":140598667,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598667,"source":"dbSNP","id":"rs1030323280","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1197433199","end":140598668,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140598668,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140598669,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140598669,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799371913","seq_region_name":"7"},{"clinical_significance":[],"id":"rs746123456","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598670,"feature_type":"variation","strand":1,"end":140598670,"alleles":["A","G"]},{"start":140598675,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140598675,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799372127","clinical_significance":[]},{"clinical_significance":[],"id":"rs17621539","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598677,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140598677},{"alleles":["AAAAAA","AAAA"],"end":140598682,"strand":1,"feature_type":"variation","start":140598677,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799372412","clinical_significance":[]},{"alleles":["T","C"],"end":140598687,"feature_type":"variation","strand":1,"source":"dbSNP","start":140598687,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799372521"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598691,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140598691,"clinical_significance":[],"seq_region_name":"7","id":"rs914881420"},{"clinical_significance":[],"id":"rs1799372740","seq_region_name":"7","end":140598695,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140598695,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140598706,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598706,"source":"dbSNP","id":"rs1799372866","seq_region_name":"7","clinical_significance":[]},{"id":"rs554701470","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598713,"source":"dbSNP","strand":1,"feature_type":"variation","end":140598713,"alleles":["G","T"]},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140598714,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598714,"source":"dbSNP","seq_region_name":"7","id":"rs1799373143","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130678852","source":"dbSNP","start":140598716,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140598716,"alleles":["T","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs566644195","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140598717,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598717,"source":"dbSNP"},{"seq_region_name":"7","id":"rs950470529","clinical_significance":[],"start":140598719,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140598719,"alleles":["G","A","T"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140598720,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140598720,"alleles":["A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs977818013"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799373891","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598723,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140598723},{"source":"dbSNP","start":140598727,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140598727,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs987229534"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598738,"feature_type":"variation","strand":1,"end":140598738,"alleles":["C","A","T"],"clinical_significance":[],"id":"rs923798583","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598739,"feature_type":"variation","strand":1,"end":140598739,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1018583934"},{"end":140598740,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140598740,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs964372709"},{"feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140598741,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598741,"clinical_significance":[],"seq_region_name":"7","id":"rs1409258046"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598744,"source":"dbSNP","strand":1,"feature_type":"variation","end":140598744,"alleles":["A","C"],"seq_region_name":"7","id":"rs1799375115","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598744,"feature_type":"variation","strand":1,"end":140598751,"alleles":["ATGTCAAA","-"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799375287"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598749,"source":"dbSNP","strand":1,"feature_type":"variation","end":140598749,"alleles":["A","T"],"seq_region_name":"7","id":"rs939173790","clinical_significance":[]},{"start":140598750,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140598750,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799375648","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1355397654","source":"dbSNP","start":140598752,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","-"],"end":140598752,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["-","C"],"end":140598753,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598754,"source":"dbSNP","seq_region_name":"7","id":"rs1799375998","clinical_significance":[]},{"source":"dbSNP","start":140598754,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140598754,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1235944923"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1237509186","source":"dbSNP","start":140598755,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140598755,"alleles":["T","G"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140598757,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598757,"source":"dbSNP","seq_region_name":"7","id":"rs1056424213","clinical_significance":[]},{"id":"rs1267152429","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140598759,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598759,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs770009868","alleles":["T","C","G"],"end":140598760,"feature_type":"variation","strand":1,"source":"dbSNP","start":140598760,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1799377131","clinical_significance":[],"alleles":["A","G"],"end":140598764,"strand":1,"feature_type":"variation","start":140598764,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1799377324","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140598771,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598771,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799377474","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140598773,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598773,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1353464289","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598774,"feature_type":"variation","strand":1,"end":140598774,"alleles":["A","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs946649642","feature_type":"variation","strand":1,"end":140598775,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598775},{"id":"rs1799377836","seq_region_name":"7","clinical_significance":[],"alleles":["C","G"],"end":140598776,"strand":1,"feature_type":"variation","start":140598776,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1242015941","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598779,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140598779},{"strand":1,"feature_type":"variation","end":140598782,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598782,"source":"dbSNP","seq_region_name":"7","id":"rs1693979016","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799378044","alleles":["A","G"],"end":140598784,"feature_type":"variation","strand":1,"source":"dbSNP","start":140598784,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140598785,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140598785,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799378190"},{"feature_type":"variation","strand":1,"end":140598790,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598790,"clinical_significance":[],"id":"rs1799378298","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1375001728","alleles":["G","A"],"end":140598791,"feature_type":"variation","strand":1,"source":"dbSNP","start":140598791,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1210918555","end":140598793,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140598793,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["T","C"],"end":140598794,"strand":1,"feature_type":"variation","start":140598794,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1441747569","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs916488792","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598795,"feature_type":"variation","strand":1,"end":140598795,"alleles":["G","A"]},{"clinical_significance":[],"id":"rs569603396","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598801,"feature_type":"variation","strand":1,"alleles":["TTT","TTTT"],"end":140598803},{"source":"dbSNP","start":140598804,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140598804,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs533992127"},{"strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140598805,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598805,"source":"dbSNP","seq_region_name":"7","id":"rs558608320","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598806,"feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140598806,"clinical_significance":[],"seq_region_name":"7","id":"rs1585726376"},{"seq_region_name":"7","id":"rs1799379277","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598810,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140598810},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598811,"feature_type":"variation","strand":1,"end":140598811,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799379387"},{"start":140598821,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140598821,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1369731448","clinical_significance":[]},{"source":"dbSNP","start":140598822,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140598822,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1291851021"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799379721","source":"dbSNP","start":140598835,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140598835,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1457892939","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598838,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140598838},{"alleles":["A","C","G"],"end":140598850,"feature_type":"variation","strand":1,"source":"dbSNP","start":140598850,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1346283625"},{"alleles":["G","A"],"end":140598852,"feature_type":"variation","strand":1,"source":"dbSNP","start":140598852,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799380071"},{"seq_region_name":"7","id":"rs1160864304","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598856,"source":"dbSNP","strand":1,"feature_type":"variation","end":140598860,"alleles":["TTTTT","TTTT"]},{"seq_region_name":"7","id":"rs1799380177","clinical_significance":[],"strand":1,"feature_type":"variation","end":140598866,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598866,"source":"dbSNP"},{"id":"rs1418203522","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598884,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140598884},{"strand":1,"feature_type":"variation","end":140598894,"alleles":["AAACAAACAA","AAACAA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598885,"source":"dbSNP","seq_region_name":"7","id":"rs558757136","clinical_significance":[]},{"alleles":["C","T"],"end":140598888,"strand":1,"feature_type":"variation","start":140598888,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799380522","clinical_significance":[]},{"id":"rs947963971","seq_region_name":"7","clinical_significance":[],"alleles":["A","C"],"end":140598890,"strand":1,"feature_type":"variation","start":140598890,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["AA","-"],"end":140598894,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598893,"clinical_significance":[],"id":"rs1799380751","seq_region_name":"7"},{"id":"rs1238870377","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598908,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140598908},{"clinical_significance":[],"seq_region_name":"7","id":"rs923778008","feature_type":"variation","strand":1,"end":140598915,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598915},{"seq_region_name":"7","id":"rs1799381086","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598917,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140598917},{"seq_region_name":"7","id":"rs1044390491","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598921,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140598921},{"strand":1,"feature_type":"variation","end":140598922,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598922,"source":"dbSNP","seq_region_name":"7","id":"rs1799381284","clinical_significance":[]},{"source":"dbSNP","start":140598926,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C","G"],"end":140598926,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs939411483"},{"source":"dbSNP","start":140598929,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140598929,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130679256"},{"alleles":["T","C"],"end":140598930,"feature_type":"variation","strand":1,"source":"dbSNP","start":140598930,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1188930973","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1056470426","seq_region_name":"7","source":"dbSNP","start":140598931,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["GATTA","-"],"end":140598935,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs117061560","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140598934,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598934,"source":"dbSNP"},{"end":140598936,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140598936,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799381899","seq_region_name":"7"},{"clinical_significance":[],"id":"rs753999277","seq_region_name":"7","source":"dbSNP","start":140598938,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140598938,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["A","-"],"end":140598938,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598938,"source":"dbSNP","seq_region_name":"7","id":"rs1799382118","clinical_significance":[]},{"source":"dbSNP","start":140598939,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140598947,"alleles":["TTTTTTTTT","TTTTTTTT","TTTTTTTTTT"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs948041763"},{"seq_region_name":"7","id":"rs190325286","clinical_significance":[],"end":140598941,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140598941,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1458189875","end":140598944,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140598944,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140598950,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140598950,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1314153142","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs994837522","source":"dbSNP","start":140598952,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140598952,"alleles":["A","G"],"feature_type":"variation","strand":1},{"start":140598953,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140598953,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799382992","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140598955,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598955,"clinical_significance":[],"seq_region_name":"7","id":"rs1799383155"},{"seq_region_name":"7","id":"rs1799383321","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598957,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140598957},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598959,"source":"dbSNP","strand":1,"feature_type":"variation","end":140598959,"alleles":["G","A"],"id":"rs1386252568","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598962,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140598962,"clinical_significance":[],"seq_region_name":"7","id":"rs1037067417"},{"feature_type":"variation","strand":1,"end":140598971,"alleles":["TATATATA","TATATATATA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598964,"clinical_significance":[],"id":"rs1047196564","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1799383865","seq_region_name":"7","source":"dbSNP","start":140598967,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140598967,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598968,"feature_type":"variation","strand":1,"end":140598968,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799383972"},{"clinical_significance":[],"id":"rs368851246","seq_region_name":"7","alleles":["G","C"],"end":140598972,"feature_type":"variation","strand":1,"source":"dbSNP","start":140598972,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140598973,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140598973,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799384195","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1398546128","clinical_significance":[],"alleles":["A","C","G"],"end":140598975,"strand":1,"feature_type":"variation","start":140598975,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140598977,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598977,"source":"dbSNP","seq_region_name":"7","id":"rs1799384436","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585726684","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598983,"source":"dbSNP","strand":1,"feature_type":"variation","end":140598983,"alleles":["A","G"]},{"feature_type":"variation","strand":1,"end":140598985,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140598985,"clinical_significance":[],"seq_region_name":"7","id":"rs1799384628"},{"end":140598987,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140598987,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs556590475","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140598988,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140598988,"source":"dbSNP","seq_region_name":"7","id":"rs575031511","clinical_significance":[]},{"clinical_significance":[],"id":"rs1173379425","seq_region_name":"7","end":140598996,"alleles":["ACTGACT","ACT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140598990,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1432038607","end":140599001,"alleles":["TAATTA","TA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140598996,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs891292588","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599007,"feature_type":"variation","strand":1,"end":140599007,"alleles":["A","T"]},{"clinical_significance":[],"id":"rs1195675770","seq_region_name":"7","alleles":["C","A","T"],"end":140599009,"feature_type":"variation","strand":1,"source":"dbSNP","start":140599009,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1487266936","clinical_significance":[],"end":140599013,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140599013,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs897358972","clinical_significance":[],"strand":1,"feature_type":"variation","end":140599015,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599015,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140599021,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599021,"clinical_significance":[],"id":"rs1799385874","seq_region_name":"7"},{"end":140599024,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140599024,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs542081484"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140599035,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599035,"source":"dbSNP","seq_region_name":"7","id":"rs1262280978","clinical_significance":[]},{"end":140599039,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140599039,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1211306190","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1799386265","seq_region_name":"7","end":140599043,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140599043,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599047,"feature_type":"variation","strand":1,"end":140599047,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs73165437"},{"alleles":["A","C"],"end":140599048,"strand":1,"feature_type":"variation","start":140599048,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1254444497","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599051,"feature_type":"variation","strand":1,"end":140599052,"alleles":["TT","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799386603"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1232641584","alleles":["T","C"],"end":140599054,"feature_type":"variation","strand":1,"source":"dbSNP","start":140599054,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1236429518","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140599056,"strand":1,"feature_type":"variation","start":140599056,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140599057,"alleles":["T","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599057,"source":"dbSNP","seq_region_name":"7","id":"rs1308083957","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799387008","clinical_significance":[],"start":140599062,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140599062,"strand":1,"feature_type":"variation"},{"start":140599063,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140599063,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1018699471","clinical_significance":[]},{"seq_region_name":"7","id":"rs1563168528","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140599066,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599066,"source":"dbSNP"},{"end":140599068,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140599068,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1029795691","seq_region_name":"7"},{"seq_region_name":"7","id":"rs527873567","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599069,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140599069},{"start":140599072,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140599072,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs1313911023","seq_region_name":"7","clinical_significance":[]},{"end":140599074,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140599074,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs2130679607","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs373397873","clinical_significance":[],"strand":1,"feature_type":"variation","end":140599085,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599085,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799387698","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140599086,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599086,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599090,"source":"dbSNP","strand":1,"feature_type":"variation","end":140599090,"alleles":["A","G"],"seq_region_name":"7","id":"rs1403929341","clinical_significance":[]},{"seq_region_name":"7","id":"rs771334011","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140599093,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599093,"source":"dbSNP"},{"start":140599096,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140599096,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799388067","clinical_significance":[]},{"end":140599099,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140599099,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1022397068","clinical_significance":[]},{"clinical_significance":[],"id":"rs2130679661","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599103,"feature_type":"variation","strand":1,"end":140599103,"alleles":["A","G"]},{"alleles":["G","A"],"end":140599109,"strand":1,"feature_type":"variation","start":140599109,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1021993318","clinical_significance":[]},{"alleles":["T","C"],"end":140599115,"strand":1,"feature_type":"variation","start":140599115,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1799388275","seq_region_name":"7","clinical_significance":[]},{"end":140599118,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140599118,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1245958941","clinical_significance":[]},{"id":"rs1799388477","seq_region_name":"7","clinical_significance":[],"end":140599122,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140599122,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs967692895","source":"dbSNP","start":140599126,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140599126,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1476829318","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140599127,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599127,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140599129,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599129,"source":"dbSNP","seq_region_name":"7","id":"rs1422794479","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599130,"feature_type":"variation","strand":1,"end":140599130,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1188035695"},{"feature_type":"variation","strand":1,"end":140599131,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599131,"clinical_significance":[],"seq_region_name":"7","id":"rs1799388928"},{"clinical_significance":[],"seq_region_name":"7","id":"rs540357594","alleles":["C","T"],"end":140599134,"feature_type":"variation","strand":1,"source":"dbSNP","start":140599134,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs768995751","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599135,"source":"dbSNP","strand":1,"feature_type":"variation","end":140599135,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799389261","end":140599139,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140599139,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140599140,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140599140,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1200160614"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599141,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140599141,"seq_region_name":"7","id":"rs977870393","clinical_significance":[]},{"seq_region_name":"7","id":"rs1481073973","clinical_significance":[],"alleles":["C","G"],"end":140599148,"strand":1,"feature_type":"variation","start":140599148,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs967957403","seq_region_name":"7","source":"dbSNP","start":140599151,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140599151,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140599153,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599153,"source":"dbSNP","seq_region_name":"7","id":"rs269242","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799389988","clinical_significance":[],"alleles":["G","A"],"end":140599156,"strand":1,"feature_type":"variation","start":140599156,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140599157,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140599157,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799390104"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799390219","alleles":["G","A"],"end":140599158,"feature_type":"variation","strand":1,"source":"dbSNP","start":140599158,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599162,"feature_type":"variation","strand":1,"alleles":["CCC","CC"],"end":140599164,"clinical_significance":[],"seq_region_name":"7","id":"rs1799390333"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1317867869","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599166,"feature_type":"variation","strand":1,"end":140599166,"alleles":["G","A"]},{"alleles":["C","T"],"end":140599182,"feature_type":"variation","strand":1,"source":"dbSNP","start":140599182,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs960449708"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599183,"source":"dbSNP","strand":1,"feature_type":"variation","end":140599188,"alleles":["AAAAAA","AAAAA"],"id":"rs1799390699","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs960813829","clinical_significance":[],"end":140599188,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140599188,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140599191,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140599191,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs992410425","clinical_significance":[]},{"seq_region_name":"7","id":"rs1176894771","clinical_significance":[],"start":140599192,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140599192,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1312458018","seq_region_name":"7","alleles":["C","G"],"end":140599194,"feature_type":"variation","strand":1,"source":"dbSNP","start":140599194,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs916644970","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140599196,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599196},{"strand":1,"feature_type":"variation","alleles":["G","C","T"],"end":140599197,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599197,"source":"dbSNP","id":"rs1237774927","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","T"],"end":140599198,"feature_type":"variation","strand":1,"source":"dbSNP","start":140599198,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1332840937"},{"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140599199,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599199,"source":"dbSNP","seq_region_name":"7","id":"rs186469308","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585727190","feature_type":"variation","strand":1,"end":140599205,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599205},{"source":"dbSNP","start":140599206,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140599206,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799391947"},{"seq_region_name":"7","id":"rs772222875","clinical_significance":[],"strand":1,"feature_type":"variation","end":140599207,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599207,"source":"dbSNP"},{"end":140599210,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140599210,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs576856396","seq_region_name":"7"},{"clinical_significance":[],"id":"rs560447221","seq_region_name":"7","alleles":["G","A"],"end":140599211,"feature_type":"variation","strand":1,"source":"dbSNP","start":140599211,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140599212,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140599212,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs941360318"},{"seq_region_name":"7","id":"rs1440590019","clinical_significance":[],"end":140599215,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140599215,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1799392653","clinical_significance":[],"strand":1,"feature_type":"variation","end":140599217,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599217,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1036952678","seq_region_name":"7","source":"dbSNP","start":140599219,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140599219,"alleles":["T","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799392885","feature_type":"variation","strand":1,"end":140599220,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599220},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585727272","feature_type":"variation","strand":1,"end":140599221,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599221},{"clinical_significance":[],"id":"rs1176877867","seq_region_name":"7","feature_type":"variation","strand":1,"end":140599222,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599222},{"end":140599229,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140599229,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1457325243","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799393344","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140599232,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599232},{"seq_region_name":"7","id":"rs1274362493","clinical_significance":[],"alleles":["G","A"],"end":140599233,"strand":1,"feature_type":"variation","start":140599233,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs139306275","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140599239,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599239,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140599244,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599244,"clinical_significance":[],"seq_region_name":"7","id":"rs1799393664"},{"seq_region_name":"7","id":"rs376600674","clinical_significance":[],"strand":1,"feature_type":"variation","end":140599246,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599246,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140599256,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599256,"source":"dbSNP","seq_region_name":"7","id":"rs1799393894","clinical_significance":[]},{"end":140599258,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140599258,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1354847092","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140599263,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599263,"clinical_significance":[],"id":"rs1799394115","seq_region_name":"7"},{"alleles":["G","A"],"end":140599267,"feature_type":"variation","strand":1,"source":"dbSNP","start":140599267,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1265278647"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599268,"feature_type":"variation","strand":1,"end":140599268,"alleles":["G","A"],"clinical_significance":[],"id":"rs1240170657","seq_region_name":"7"},{"seq_region_name":"7","id":"rs761823360","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599269,"source":"dbSNP","strand":1,"feature_type":"variation","end":140599269,"alleles":["T","C","G"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599273,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140599273,"clinical_significance":[],"seq_region_name":"7","id":"rs1799394473"},{"clinical_significance":[],"seq_region_name":"7","id":"rs930207054","feature_type":"variation","strand":1,"end":140599277,"alleles":["G","C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599277},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799394736","feature_type":"variation","strand":1,"end":140599279,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599279},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599281,"source":"dbSNP","strand":1,"feature_type":"variation","end":140599281,"alleles":["T","C"],"seq_region_name":"7","id":"rs998250208","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs34402559","feature_type":"variation","strand":1,"alleles":["T","TT"],"end":140599286,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599286},{"start":140599287,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140599287,"alleles":["G","T"],"strand":1,"feature_type":"variation","id":"rs1799395032","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140599288,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140599288,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1330155540"},{"seq_region_name":"7","id":"rs1799395252","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599291,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140599291},{"feature_type":"variation","strand":1,"end":140599292,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599292,"clinical_significance":[],"id":"rs1310935921","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599293,"feature_type":"variation","strand":1,"end":140599293,"alleles":["G","GG"],"clinical_significance":[],"seq_region_name":"7","id":"rs1406341099"},{"alleles":["G","C"],"end":140599295,"feature_type":"variation","strand":1,"source":"dbSNP","start":140599295,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1375603016"},{"id":"rs1799395666","seq_region_name":"7","clinical_significance":[],"start":140599300,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140599300,"strand":1,"feature_type":"variation"},{"alleles":["A","G"],"end":140599301,"feature_type":"variation","strand":1,"source":"dbSNP","start":140599301,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130680167"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599305,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140599305,"clinical_significance":[],"seq_region_name":"7","id":"rs764944750"},{"feature_type":"variation","strand":1,"end":140599306,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599306,"clinical_significance":[],"id":"rs537733884","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563168687","end":140599308,"alleles":["A","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140599308,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140599315,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140599315,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799396127","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799396234","clinical_significance":[],"start":140599316,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140599316,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599317,"feature_type":"variation","strand":1,"end":140599317,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs562642155"},{"clinical_significance":[],"id":"rs1799396420","seq_region_name":"7","source":"dbSNP","start":140599319,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140599319,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1039919925","clinical_significance":[],"alleles":["T","C","G"],"end":140599322,"strand":1,"feature_type":"variation","start":140599322,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599323,"source":"dbSNP","strand":1,"feature_type":"variation","end":140599323,"alleles":["C","T"],"id":"rs1420030213","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799396770","seq_region_name":"7","end":140599324,"alleles":["T","TTGT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140599324,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140599325,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599325,"source":"dbSNP","id":"rs1382411905","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799397011","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599326,"feature_type":"variation","strand":1,"end":140599326,"alleles":["T","C"]},{"end":140599327,"alleles":["C","A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140599327,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1315205078"},{"alleles":["C","T"],"end":140599329,"feature_type":"variation","strand":1,"source":"dbSNP","start":140599329,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1007176907"},{"start":140599330,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140599330,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs1022546980","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599331,"source":"dbSNP","strand":1,"feature_type":"variation","end":140599331,"alleles":["A","G"],"seq_region_name":"7","id":"rs1799397478","clinical_significance":[]},{"start":140599331,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AAAAAAAAA","AAAAAAAA","AAAAAAAAAA"],"end":140599339,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs199973107","clinical_significance":[]},{"seq_region_name":"7","id":"rs6974314","clinical_significance":[],"strand":1,"feature_type":"variation","end":140599337,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599337,"source":"dbSNP"},{"start":140599338,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140599353,"alleles":["AATAATAATAATAATA","AATAATAATA","AATAATAATAATAATAATA"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs999232903","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799397890","clinical_significance":[],"start":140599339,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140599339,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599340,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140599340,"clinical_significance":[],"seq_region_name":"7","id":"rs73165439"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799398144","source":"dbSNP","start":140599340,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140599340,"alleles":["T","-"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599342,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140599342,"clinical_significance":[],"id":"rs1356227700","seq_region_name":"7"},{"source":"dbSNP","start":140599343,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140599343,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1284317409"},{"feature_type":"variation","strand":1,"end":140599351,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599351,"clinical_significance":[],"seq_region_name":"7","id":"rs1799398425"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140599353,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599353,"clinical_significance":[],"seq_region_name":"7","id":"rs1279351524"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599355,"source":"dbSNP","strand":1,"feature_type":"variation","end":140599355,"alleles":["A","G"],"seq_region_name":"7","id":"rs1585727644","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs181074051","end":140599359,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140599359,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1799398874","clinical_significance":[],"strand":1,"feature_type":"variation","end":140599360,"alleles":["G","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599360,"source":"dbSNP"},{"alleles":["A","C"],"end":140599368,"strand":1,"feature_type":"variation","start":140599368,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1274966185","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140599369,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599369,"clinical_significance":[],"seq_region_name":"7","id":"rs1563168726"},{"end":140599379,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140599379,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799399209","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599380,"source":"dbSNP","strand":1,"feature_type":"variation","end":140599380,"alleles":["G","A","T"],"seq_region_name":"7","id":"rs1799399299","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799399429","feature_type":"variation","strand":1,"end":140599385,"alleles":["G","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599385},{"clinical_significance":[],"id":"rs201071397","seq_region_name":"7","source":"dbSNP","start":140599386,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AAAAAAAAA","AAAAAAAA","AAAAAAAAAA"],"end":140599394,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1322742465","source":"dbSNP","start":140599387,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140599387,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1400384550","clinical_significance":[],"strand":1,"feature_type":"variation","end":140599392,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599392,"source":"dbSNP"},{"source":"dbSNP","start":140599395,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140599395,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1196809719","seq_region_name":"7"},{"seq_region_name":"7","id":"rs149441684","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599398,"source":"dbSNP","strand":1,"feature_type":"variation","end":140599398,"alleles":["C","G"]},{"source":"dbSNP","start":140599401,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140599401,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs6952059"},{"clinical_significance":[],"id":"rs1799400222","seq_region_name":"7","alleles":["T","C"],"end":140599403,"feature_type":"variation","strand":1,"source":"dbSNP","start":140599403,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599404,"source":"dbSNP","strand":1,"feature_type":"variation","end":140599417,"alleles":["TAATTAAACAGAAT","T"],"seq_region_name":"7","id":"rs1419383739","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140599404,"alleles":["-","GGAGCCAGAGAAA","GGAGCCAGAGAAAAATAAAATGGAGCCAGAGAAAAATAA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599405,"clinical_significance":[],"id":"rs1202415294","seq_region_name":"7"},{"end":140599407,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140599407,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799400576"},{"clinical_significance":[],"id":"rs1253764378","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["-","AAAA"],"end":140599407,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599408},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799400808","feature_type":"variation","strand":1,"end":140599408,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599408},{"clinical_significance":[],"seq_region_name":"7","id":"rs1423062341","feature_type":"variation","strand":1,"end":140599408,"alleles":["-","GGAGCCAGAGAAAAATAAAAAA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599409},{"seq_region_name":"7","id":"rs916458465","clinical_significance":[],"end":140599415,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140599415,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1174420639","end":140599422,"alleles":["C","A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140599422,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1194169909","clinical_significance":[],"strand":1,"feature_type":"variation","end":140599426,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599426,"source":"dbSNP"},{"alleles":["G","A"],"end":140599427,"strand":1,"feature_type":"variation","start":140599427,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1477054674","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140599431,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599431,"clinical_significance":[],"seq_region_name":"7","id":"rs1799401471"},{"alleles":["T","C"],"end":140599433,"feature_type":"variation","strand":1,"source":"dbSNP","start":140599433,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs929961304"},{"strand":1,"feature_type":"variation","alleles":["AAAA","AAA"],"end":140599437,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599434,"source":"dbSNP","seq_region_name":"7","id":"rs1194944650","clinical_significance":[]},{"id":"rs1799401793","seq_region_name":"7","clinical_significance":[],"alleles":["A","G"],"end":140599437,"strand":1,"feature_type":"variation","start":140599437,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1489549035","source":"dbSNP","start":140599443,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140599448,"alleles":["CACACA","CA"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs762281095","clinical_significance":[],"strand":1,"feature_type":"variation","end":140599445,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599445,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1261542234","clinical_significance":[],"start":140599447,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140599447,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140599449,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599449,"source":"dbSNP","id":"rs2130680588","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140599450,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599450,"clinical_significance":[],"id":"rs1216303257","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1446096400","end":140599452,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140599452,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","T"],"end":140599456,"feature_type":"variation","strand":1,"source":"dbSNP","start":140599456,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799402322"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140599459,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599459,"source":"dbSNP","seq_region_name":"7","id":"rs1799402431","clinical_significance":[]},{"clinical_significance":[],"id":"rs1585727902","seq_region_name":"7","feature_type":"variation","strand":1,"end":140599463,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599463},{"source":"dbSNP","start":140599464,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140599464,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130680624"},{"seq_region_name":"7","id":"rs143025151","clinical_significance":[],"start":140599466,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140599466,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1799402755","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599467,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140599467},{"seq_region_name":"7","id":"rs1799402855","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140599469,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599469,"source":"dbSNP"},{"id":"rs1799402972","seq_region_name":"7","clinical_significance":[],"end":140599470,"alleles":["AA","-"],"strand":1,"feature_type":"variation","start":140599469,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599477,"source":"dbSNP","strand":1,"feature_type":"variation","end":140599477,"alleles":["G","A"],"id":"rs78791317","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140599481,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599481,"clinical_significance":[],"seq_region_name":"7","id":"rs912790101"},{"start":140599483,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140599483,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585727933","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799403443","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140599491,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599491},{"clinical_significance":[],"seq_region_name":"7","id":"rs909049368","alleles":["A","C"],"end":140599498,"feature_type":"variation","strand":1,"source":"dbSNP","start":140599498,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1799403667","clinical_significance":[],"alleles":["T","C"],"end":140599500,"strand":1,"feature_type":"variation","start":140599500,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140599505,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["ACAACAAC","ACAAC"],"end":140599512,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799403776"},{"clinical_significance":[],"seq_region_name":"7","id":"rs940563887","alleles":["C","T"],"end":140599509,"feature_type":"variation","strand":1,"source":"dbSNP","start":140599509,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1799403991","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599511,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140599511},{"clinical_significance":[],"seq_region_name":"7","id":"rs972780067","source":"dbSNP","start":140599514,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140599514,"alleles":["C","T"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599519,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140599519,"seq_region_name":"7","id":"rs1799404203","clinical_significance":[]},{"alleles":["G","A"],"end":140599521,"feature_type":"variation","strand":1,"source":"dbSNP","start":140599521,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1342171776","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140599523,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599523,"clinical_significance":[],"seq_region_name":"7","id":"rs1282081789"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799404512","source":"dbSNP","start":140599525,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140599525,"feature_type":"variation","strand":1},{"alleles":["A","C"],"end":140599527,"feature_type":"variation","strand":1,"source":"dbSNP","start":140599527,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799404613"},{"id":"rs756864940","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140599539,"alleles":["TATAATATAAT","TATAAT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599529,"source":"dbSNP"},{"seq_region_name":"7","id":"rs918704350","clinical_significance":[],"end":140599531,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140599531,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599537,"feature_type":"variation","strand":1,"end":140599537,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130680768"},{"seq_region_name":"7","id":"rs1169336204","clinical_significance":[],"end":140599542,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140599542,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1276117596","seq_region_name":"7","clinical_significance":[],"end":140599543,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140599543,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1799405491","seq_region_name":"7","clinical_significance":[],"start":140599545,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G","T"],"end":140599545,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799405718","alleles":["T","G"],"end":140599550,"feature_type":"variation","strand":1,"source":"dbSNP","start":140599550,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140599553,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140599553,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799405917"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1399125634","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599555,"feature_type":"variation","strand":1,"end":140599555,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585728033","source":"dbSNP","start":140599557,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A","C"],"end":140599557,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140599576,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140599576,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799406498"},{"clinical_significance":[],"seq_region_name":"7","id":"rs933962554","source":"dbSNP","start":140599583,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140599583,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599584,"source":"dbSNP","strand":1,"feature_type":"variation","end":140599584,"alleles":["G","A"],"seq_region_name":"7","id":"rs1336340991","clinical_significance":[]},{"start":140599585,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140599585,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799406902","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140599593,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599593,"clinical_significance":[],"seq_region_name":"7","id":"rs1051115820"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599594,"feature_type":"variation","strand":1,"end":140599594,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1359250186"},{"clinical_significance":[],"seq_region_name":"7","id":"rs890000958","source":"dbSNP","start":140599595,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C","G"],"end":140599595,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1799407375","clinical_significance":[],"alleles":["A","G"],"end":140599596,"strand":1,"feature_type":"variation","start":140599596,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140599600,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599600,"source":"dbSNP","seq_region_name":"7","id":"rs1467217522","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599602,"source":"dbSNP","strand":1,"feature_type":"variation","end":140599602,"alleles":["C","T"],"seq_region_name":"7","id":"rs1171448063","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599604,"source":"dbSNP","strand":1,"feature_type":"variation","end":140599604,"alleles":["C","T"],"id":"rs942932508","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799407788","source":"dbSNP","start":140599610,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140599610,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1479110908","alleles":["T","TT"],"end":140599611,"feature_type":"variation","strand":1,"source":"dbSNP","start":140599611,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1799408003","clinical_significance":[],"start":140599613,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140599613,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140599614,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599614,"clinical_significance":[],"id":"rs1799408120","seq_region_name":"7"},{"start":140599615,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140599615,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs148200832","seq_region_name":"7","clinical_significance":[]},{"id":"rs904013946","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140599616,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599616,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1799408436","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140599618,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599618},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599621,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140599621,"clinical_significance":[],"id":"rs531924930","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1414526352","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599634,"source":"dbSNP","strand":1,"feature_type":"variation","end":140599634,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1237696530","alleles":["T","A","C"],"end":140599635,"feature_type":"variation","strand":1,"source":"dbSNP","start":140599635,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs536181519","clinical_significance":[],"strand":1,"feature_type":"variation","end":140599636,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599636,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140599638,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599638,"source":"dbSNP","seq_region_name":"7","id":"rs947575211","clinical_significance":[]},{"start":140599641,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140599641,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130680964","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599645,"source":"dbSNP","strand":1,"feature_type":"variation","end":140599645,"alleles":["A","G"],"seq_region_name":"7","id":"rs1799409199","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1262024029","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140599646,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599646},{"start":140599648,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140599648,"strand":1,"feature_type":"variation","id":"rs1799409420","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","T"],"end":140599649,"strand":1,"feature_type":"variation","start":140599649,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1299252017","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799409625","alleles":["A","-"],"end":140599650,"feature_type":"variation","strand":1,"source":"dbSNP","start":140599650,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1799409738","seq_region_name":"7","clinical_significance":[],"start":140599653,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140599653,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1198692672","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140599654,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599654,"source":"dbSNP"},{"seq_region_name":"7","id":"rs369387992","clinical_significance":[],"alleles":["T","G"],"end":140599657,"strand":1,"feature_type":"variation","start":140599657,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599659,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140599659,"clinical_significance":[],"seq_region_name":"7","id":"rs1256025832"},{"start":140599666,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140599666,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799410161","clinical_significance":[]},{"end":140599668,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140599668,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs903629934","clinical_significance":[]},{"source":"dbSNP","start":140599670,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140599670,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs572724221"},{"id":"rs1799410532","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140599696,"alleles":["ATAACTTATATATATTTACATATATA","ATA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599671,"source":"dbSNP"},{"id":"rs1013638835","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","G"],"end":140599675,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599675,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799410795","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599676,"source":"dbSNP","strand":1,"feature_type":"variation","end":140599676,"alleles":["T","A"]},{"feature_type":"variation","strand":1,"end":140599677,"alleles":["TT","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599676,"clinical_significance":[],"seq_region_name":"7","id":"rs1799410936"},{"end":140599685,"alleles":["TATATATAT","TATATATATAT"],"strand":1,"feature_type":"variation","start":140599677,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799411057","clinical_significance":[]},{"id":"rs1312874374","seq_region_name":"7","clinical_significance":[],"start":140599678,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140599678,"alleles":["A","C","G","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1799411733","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140599681,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599681,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140599685,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599685,"source":"dbSNP","seq_region_name":"7","id":"rs1379541061","clinical_significance":[]},{"seq_region_name":"7","id":"rs1030683604","clinical_significance":[],"start":140599690,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["ATATATATATA","ATATATATA","ATATATATATATA"],"end":140599700,"strand":1,"feature_type":"variation"},{"id":"rs1799412413","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140599691,"strand":1,"feature_type":"variation","start":140599691,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1254455488","source":"dbSNP","start":140599693,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140599693,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs544799651","seq_region_name":"7","source":"dbSNP","start":140599695,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140599695,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs560226457","source":"dbSNP","start":140599699,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140599699,"alleles":["T","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1467204823","source":"dbSNP","start":140599701,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140599701,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1799413375","clinical_significance":[],"end":140599704,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140599704,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799413559","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140599705,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599705},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599706,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140599706,"clinical_significance":[],"seq_region_name":"7","id":"rs1023387298"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599709,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140599709,"seq_region_name":"7","id":"rs1799413837","clinical_significance":[]},{"alleles":["T","G"],"end":140599720,"feature_type":"variation","strand":1,"source":"dbSNP","start":140599720,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799413950"},{"seq_region_name":"7","id":"rs1398749813","clinical_significance":[],"end":140599721,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140599721,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799414179","source":"dbSNP","start":140599724,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140599724,"alleles":["G","C"],"feature_type":"variation","strand":1},{"end":140599729,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140599729,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs572021957"},{"seq_region_name":"7","id":"rs2130681212","clinical_significance":[],"alleles":["G","A"],"end":140599730,"strand":1,"feature_type":"variation","start":140599730,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140599731,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140599731,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1487234767"},{"id":"rs1799414581","seq_region_name":"7","clinical_significance":[],"end":140599732,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140599732,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599736,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140599736,"seq_region_name":"7","id":"rs1406451699","clinical_significance":[]},{"source":"dbSNP","start":140599736,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140599740,"alleles":["TTTTT","TTTT"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1192883840"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599739,"source":"dbSNP","strand":1,"feature_type":"variation","end":140599739,"alleles":["T","C"],"seq_region_name":"7","id":"rs1799414995","clinical_significance":[]},{"end":140599740,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140599740,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799415110","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1180460316","clinical_significance":[],"start":140599742,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140599742,"alleles":["C","G","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1471631348","clinical_significance":[],"start":140599750,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140599750,"alleles":["A","C","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1799415529","seq_region_name":"7","source":"dbSNP","start":140599751,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140599751,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs2130681286","clinical_significance":[],"strand":1,"feature_type":"variation","end":140599753,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599753,"source":"dbSNP"},{"clinical_significance":[],"id":"rs973968608","seq_region_name":"7","source":"dbSNP","start":140599757,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C","G"],"end":140599757,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599758,"feature_type":"variation","strand":1,"end":140599758,"alleles":["C","T"],"clinical_significance":[],"id":"rs2130681304","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599760,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140599760,"id":"rs1799415966","seq_region_name":"7","clinical_significance":[]},{"start":140599767,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140599767,"alleles":["A","G"],"strand":1,"feature_type":"variation","id":"rs1799416082","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799416195","clinical_significance":[],"start":140599769,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140599769,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599772,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140599772,"clinical_significance":[],"seq_region_name":"7","id":"rs1799416318"},{"strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140599776,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599776,"source":"dbSNP","seq_region_name":"7","id":"rs1434364524","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs984666415","feature_type":"variation","strand":1,"end":140599778,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599778},{"seq_region_name":"7","id":"rs186511502","clinical_significance":[],"alleles":["T","C"],"end":140599779,"strand":1,"feature_type":"variation","start":140599779,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs2130681363","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599788,"feature_type":"variation","strand":1,"end":140599788,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs1799416857","clinical_significance":[],"start":140599789,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140599789,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"start":140599792,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140599792,"strand":1,"feature_type":"variation","id":"rs1799416971","seq_region_name":"7","clinical_significance":[]},{"start":140599795,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140599795,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs961836254","clinical_significance":[]},{"alleles":["GGGG","GGGGG"],"end":140599798,"feature_type":"variation","strand":1,"source":"dbSNP","start":140599795,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799417201"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799417317","source":"dbSNP","start":140599798,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140599798,"alleles":["G","A"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140599799,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599799,"clinical_significance":[],"seq_region_name":"7","id":"rs971941906"},{"clinical_significance":[],"seq_region_name":"7","id":"rs951519510","feature_type":"variation","strand":1,"end":140599806,"alleles":["AAAAAAAA","AAAAAAA","AAAAAAAAA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599799},{"id":"rs1799417714","seq_region_name":"7","clinical_significance":[],"start":140599800,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140599800,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140599807,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599807,"clinical_significance":[],"seq_region_name":"7","id":"rs1310185397"},{"clinical_significance":[],"id":"rs1799417943","seq_region_name":"7","feature_type":"variation","strand":1,"end":140599810,"alleles":["AAA","AA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599808},{"source":"dbSNP","start":140599810,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140599810,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799418068"},{"start":140599814,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140599814,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130681443","clinical_significance":[]},{"end":140599818,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140599818,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1449092864","clinical_significance":[]},{"seq_region_name":"7","id":"rs576964464","clinical_significance":[],"start":140599826,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140599826,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs934099180","clinical_significance":[],"strand":1,"feature_type":"variation","end":140599827,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599827,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140599834,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599834,"source":"dbSNP","id":"rs1159554059","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140599838,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599838,"source":"dbSNP","seq_region_name":"7","id":"rs987166613","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599844,"feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140599844,"clinical_significance":[],"id":"rs1437872981","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599845,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140599845,"clinical_significance":[],"seq_region_name":"7","id":"rs1352096045"},{"alleles":["A","G"],"end":140599851,"feature_type":"variation","strand":1,"source":"dbSNP","start":140599851,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs373269461"},{"source":"dbSNP","start":140599852,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140599852,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs912581147"},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140599853,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599853,"source":"dbSNP","id":"rs1799419209","seq_region_name":"7","clinical_significance":[]},{"id":"rs1362865009","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140599858,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599858,"source":"dbSNP"},{"start":140599861,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140599861,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs118090819","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140599863,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599863,"source":"dbSNP","seq_region_name":"7","id":"rs911223667","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140599868,"alleles":["GGGGGG","GGGGG","GGGGGGG"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599863,"clinical_significance":[],"seq_region_name":"7","id":"rs1288832350"},{"alleles":["G","A"],"end":140599864,"strand":1,"feature_type":"variation","start":140599864,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799419904","clinical_significance":[]},{"end":140599865,"alleles":["G","C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140599865,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1488784499"},{"clinical_significance":[],"seq_region_name":"7","id":"rs942711485","source":"dbSNP","start":140599866,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140599866,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140599867,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599867,"clinical_significance":[],"seq_region_name":"7","id":"rs1799420272"},{"start":140599868,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140599868,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs975658667","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585728690","clinical_significance":[],"alleles":["T","A"],"end":140599869,"strand":1,"feature_type":"variation","start":140599869,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1248335504","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599870,"source":"dbSNP","strand":1,"feature_type":"variation","end":140599870,"alleles":["G","A"]},{"end":140599872,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140599872,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1799420732","seq_region_name":"7","clinical_significance":[]},{"start":140599873,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140599873,"strand":1,"feature_type":"variation","id":"rs2130681609","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599874,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140599874,"clinical_significance":[],"seq_region_name":"7","id":"rs1799420851"},{"seq_region_name":"7","id":"rs1043986896","clinical_significance":[],"alleles":["A","G"],"end":140599876,"strand":1,"feature_type":"variation","start":140599876,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1799421069","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140599877,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599877,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1585728718","clinical_significance":[],"alleles":["T","C"],"end":140599886,"strand":1,"feature_type":"variation","start":140599886,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1490105355","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599894,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140599894},{"id":"rs1286463048","seq_region_name":"7","clinical_significance":[],"start":140599895,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140599895,"alleles":["T","C","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1388571926","seq_region_name":"7","end":140599905,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140599905,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140599920,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599920,"clinical_significance":[],"seq_region_name":"7","id":"rs1446803960"},{"alleles":["G","A"],"end":140599922,"strand":1,"feature_type":"variation","start":140599922,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1351750524","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599925,"feature_type":"variation","strand":1,"end":140599925,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799422062"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1306442211","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140599926,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599926},{"seq_region_name":"7","id":"rs904127906","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140599937,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599937,"source":"dbSNP"},{"id":"rs1347425261","seq_region_name":"7","clinical_significance":[],"end":140599938,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140599938,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs935460548","clinical_significance":[],"strand":1,"feature_type":"variation","end":140599939,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599939,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799423029","clinical_significance":[],"end":140599942,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140599942,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140599943,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140599943,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs754409659","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585728805","clinical_significance":[],"start":140599945,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140599945,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs2130681742","clinical_significance":[],"start":140599946,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140599946,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"start":140599947,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140599947,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799423522","clinical_significance":[]},{"id":"rs1799423620","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140599969,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599969,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140599976,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140599976,"source":"dbSNP","seq_region_name":"7","id":"rs921549005","clinical_significance":[]},{"source":"dbSNP","start":140599980,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140599980,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1563169041"},{"seq_region_name":"7","id":"rs1361651167","clinical_significance":[],"start":140599981,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140599981,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799424115","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140599982,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599982},{"clinical_significance":[],"seq_region_name":"7","id":"rs1241155978","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599983,"feature_type":"variation","strand":1,"alleles":["AGATGTAG","AG"],"end":140599990},{"clinical_significance":[],"seq_region_name":"7","id":"rs896188469","source":"dbSNP","start":140599987,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140599987,"feature_type":"variation","strand":1},{"start":140599994,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140599994,"strand":1,"feature_type":"variation","id":"rs562468814","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140599998,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140599998,"clinical_significance":[],"seq_region_name":"7","id":"rs1799424663"},{"start":140600006,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140600006,"alleles":["A","T"],"strand":1,"feature_type":"variation","id":"rs1799424775","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799424894","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140600007,"source":"dbSNP","strand":1,"feature_type":"variation","end":140600007,"alleles":["G","A"]},{"alleles":["A","T"],"end":140600013,"feature_type":"variation","strand":1,"source":"dbSNP","start":140600013,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1378055883"},{"start":140600021,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140600021,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799425090","clinical_significance":[]},{"source":"dbSNP","start":140600022,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140600022,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1157759281"},{"seq_region_name":"7","id":"rs1799425214","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140600027,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140600027,"source":"dbSNP"},{"start":140600030,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140600030,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1351273685","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799425474","clinical_significance":[],"strand":1,"feature_type":"variation","end":140600031,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140600031,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1427183145","clinical_significance":[],"start":140600032,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140600032,"strand":1,"feature_type":"variation"},{"start":140600033,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140600033,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1215677257","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799425838","clinical_significance":[],"start":140600035,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140600035,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1799425954","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140600043,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140600043,"source":"dbSNP"},{"source":"dbSNP","start":140600052,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140600052,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1043253172"},{"clinical_significance":[],"seq_region_name":"7","id":"rs529638412","alleles":["A","T"],"end":140600067,"feature_type":"variation","strand":1,"source":"dbSNP","start":140600067,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799426323","feature_type":"variation","strand":1,"end":140600069,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600069},{"clinical_significance":[],"seq_region_name":"7","id":"rs141195762","source":"dbSNP","start":140600072,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140600072,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs560008413","feature_type":"variation","strand":1,"end":140600074,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600074},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799426718","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140600075,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600075},{"seq_region_name":"7","id":"rs1585728930","clinical_significance":[],"end":140600082,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140600082,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1487450174","clinical_significance":[],"alleles":["T","C"],"end":140600087,"strand":1,"feature_type":"variation","start":140600087,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1266056772","clinical_significance":[],"start":140600088,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140600088,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"start":140600097,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140600097,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799427190","clinical_significance":[]},{"end":140600098,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140600098,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1439860226","clinical_significance":[]},{"id":"rs1799427459","seq_region_name":"7","clinical_significance":[],"start":140600101,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140600101,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1052493774","end":140600102,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140600102,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1223505389","clinical_significance":[],"strand":1,"feature_type":"variation","end":140600106,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140600106,"source":"dbSNP"},{"seq_region_name":"7","id":"rs73500424","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140600116,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140600116,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1398486468","clinical_significance":[],"start":140600117,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140600117,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799428229","source":"dbSNP","start":140600123,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140600123,"alleles":["G","A"],"feature_type":"variation","strand":1},{"start":140600124,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140600124,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1382517956","clinical_significance":[]},{"seq_region_name":"7","id":"rs1418223751","clinical_significance":[],"start":140600133,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140600133,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1287857580","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600137,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140600137},{"seq_region_name":"7","id":"rs1158904595","clinical_significance":[],"alleles":["G","C"],"end":140600138,"strand":1,"feature_type":"variation","start":140600138,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140600141,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140600141,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585729066"},{"end":140600146,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140600146,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs531511380"},{"id":"rs1350961805","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140600152,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140600152,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600153,"feature_type":"variation","strand":1,"end":140600153,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799429215"},{"strand":1,"feature_type":"variation","end":140600155,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140600155,"source":"dbSNP","seq_region_name":"7","id":"rs1799429349","clinical_significance":[]},{"source":"dbSNP","start":140600156,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140600156,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799429465","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140600158,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140600158,"seq_region_name":"7","id":"rs1799429580","clinical_significance":[]},{"start":140600159,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140600159,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1016112326","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140600160,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140600160,"seq_region_name":"7","id":"rs1799429819","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799429948","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600163,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140600163},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140600168,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600168,"clinical_significance":[],"seq_region_name":"7","id":"rs2130682118"},{"clinical_significance":[],"id":"rs1799430065","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140600169,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600169},{"id":"rs961950277","seq_region_name":"7","clinical_significance":[],"start":140600174,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C","G"],"end":140600174,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140600179,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600179,"clinical_significance":[],"seq_region_name":"7","id":"rs1799430307"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130682145","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600182,"feature_type":"variation","strand":1,"end":140600182,"alleles":["C","T"]},{"id":"rs867510992","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140600187,"source":"dbSNP","strand":1,"feature_type":"variation","end":140600187,"alleles":["G","A"]},{"clinical_significance":[],"id":"rs150736293","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600191,"feature_type":"variation","strand":1,"end":140600191,"alleles":["G","A"]},{"strand":1,"feature_type":"variation","end":140600193,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140600193,"source":"dbSNP","seq_region_name":"7","id":"rs1424205815","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs570635292","source":"dbSNP","start":140600194,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140600194,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1195608986","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140600195,"source":"dbSNP","strand":1,"feature_type":"variation","end":140600195,"alleles":["A","-"]},{"seq_region_name":"7","id":"rs1476687479","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140600195,"source":"dbSNP","strand":1,"feature_type":"variation","end":140600195,"alleles":["A","G"]},{"id":"rs756707210","seq_region_name":"7","clinical_significance":[],"end":140600196,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140600196,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140600197,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140600197,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1447745588","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799431542","source":"dbSNP","start":140600198,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140600198,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1484352234","clinical_significance":[],"start":140600200,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140600200,"strand":1,"feature_type":"variation"},{"alleles":["T","C","G"],"end":140600205,"feature_type":"variation","strand":1,"source":"dbSNP","start":140600205,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799431907"},{"seq_region_name":"7","id":"rs538303382","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140600210,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C","T"],"end":140600210},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140600212,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140600212,"source":"dbSNP","seq_region_name":"7","id":"rs1254392143","clinical_significance":[]},{"clinical_significance":[],"id":"rs1023503195","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600213,"feature_type":"variation","strand":1,"end":140600213,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799432623","end":140600217,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140600217,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs2130682278","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140600228,"source":"dbSNP","strand":1,"feature_type":"variation","end":140600228,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1203082585","source":"dbSNP","start":140600230,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140600230,"alleles":["A","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs549616344","source":"dbSNP","start":140600232,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140600232,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140600233,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600233,"clinical_significance":[],"seq_region_name":"7","id":"rs1260486510"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140600237,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140600237,"seq_region_name":"7","id":"rs1799433468","clinical_significance":[]},{"end":140600239,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140600239,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1217187113"},{"end":140600248,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140600248,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799433835","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799434018","clinical_significance":[],"strand":1,"feature_type":"variation","end":140600250,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140600250,"source":"dbSNP"},{"end":140600251,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140600251,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1326275660","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563169173","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140600260,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600260},{"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140600263,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600263,"clinical_significance":[],"id":"rs986896094","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140600266,"alleles":["G","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600266,"clinical_significance":[],"seq_region_name":"7","id":"rs1313861703"},{"source":"dbSNP","start":140600267,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140600267,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799434991","seq_region_name":"7"},{"source":"dbSNP","start":140600271,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140600271,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1396297167"},{"seq_region_name":"7","id":"rs191330035","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140600275,"source":"dbSNP","strand":1,"feature_type":"variation","end":140600275,"alleles":["G","A"]},{"alleles":["G","A"],"end":140600278,"feature_type":"variation","strand":1,"source":"dbSNP","start":140600278,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799435361"},{"alleles":["G","C"],"end":140600281,"strand":1,"feature_type":"variation","start":140600281,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1334161328","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1222979823","source":"dbSNP","start":140600288,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140600288,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140600292,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140600292,"source":"dbSNP","id":"rs564958692","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600294,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140600294,"clinical_significance":[],"seq_region_name":"7","id":"rs911338181"},{"strand":1,"feature_type":"variation","end":140600296,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140600296,"source":"dbSNP","seq_region_name":"7","id":"rs1799436071","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["GGG","GGGG"],"end":140600300,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140600298,"source":"dbSNP","id":"rs34794418","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs995730050","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600301,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140600301},{"seq_region_name":"7","id":"rs1290410101","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140600305,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140600305,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140600317,"source":"dbSNP","strand":1,"feature_type":"variation","end":140600317,"alleles":["T","C"],"seq_region_name":"7","id":"rs1799436585","clinical_significance":[]},{"source":"dbSNP","start":140600321,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140600321,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799436720"},{"alleles":["T","C"],"end":140600323,"feature_type":"variation","strand":1,"source":"dbSNP","start":140600323,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs749716750"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799436984","source":"dbSNP","start":140600325,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140600325,"feature_type":"variation","strand":1},{"end":140600329,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140600329,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799437099","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1026838319","end":140600330,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140600330,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","T"],"end":140600331,"strand":1,"feature_type":"variation","start":140600331,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799437360","clinical_significance":[]},{"alleles":["A","G"],"end":140600332,"strand":1,"feature_type":"variation","start":140600332,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1323359312","clinical_significance":[]},{"end":140600333,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140600333,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs535479244"},{"start":140600334,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140600334,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs757519811","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799437902","end":140600335,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140600335,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["G","A"],"end":140600336,"feature_type":"variation","strand":1,"source":"dbSNP","start":140600336,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799438039"},{"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140600339,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600339,"clinical_significance":[],"seq_region_name":"7","id":"rs1799438147"},{"start":140600340,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140600340,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799438263","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140600343,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600343,"clinical_significance":[],"id":"rs1264303838","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1799438492","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600344,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140600344},{"clinical_significance":[],"seq_region_name":"7","id":"rs1183075119","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600347,"feature_type":"variation","strand":1,"end":140600347,"alleles":["A","C","T"]},{"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140600355,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140600355,"source":"dbSNP","id":"rs554544958","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140600360,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140600360,"source":"dbSNP","seq_region_name":"7","id":"rs1197363429","clinical_significance":[]},{"seq_region_name":"7","id":"rs572736520","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140600363,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140600363,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799439208","end":140600368,"alleles":["GTGTAG","GTGTAGGTGTAG"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140600363,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140600365,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140600365,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799439323","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140600370,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600370,"clinical_significance":[],"seq_region_name":"7","id":"rs1052991094"},{"start":140600382,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140600382,"strand":1,"feature_type":"variation","id":"rs1180016841","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799439714","feature_type":"variation","strand":1,"alleles":["G","-"],"end":140600382,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600382},{"start":140600383,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140600386,"alleles":["TCTC","TC"],"strand":1,"feature_type":"variation","id":"rs1799439830","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600384,"feature_type":"variation","strand":1,"end":140600384,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1247385232"},{"id":"rs1235959082","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140600386,"strand":1,"feature_type":"variation","start":140600386,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1438759960","clinical_significance":[],"alleles":["G","A"],"end":140600388,"strand":1,"feature_type":"variation","start":140600388,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140600389,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600389,"clinical_significance":[],"seq_region_name":"7","id":"rs1323171923"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585729490","feature_type":"variation","strand":1,"end":140600390,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600390},{"feature_type":"variation","strand":1,"end":140600391,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600391,"clinical_significance":[],"seq_region_name":"7","id":"rs1799440570"},{"seq_region_name":"7","id":"rs1176985438","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140600392,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140600392},{"seq_region_name":"7","id":"rs1451291319","clinical_significance":[],"start":140600396,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140600396,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs918085809","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600397,"feature_type":"variation","strand":1,"end":140600397,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs115691207","alleles":["G","A"],"end":140600400,"feature_type":"variation","strand":1,"source":"dbSNP","start":140600400,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140600406,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600406,"clinical_significance":[],"seq_region_name":"7","id":"rs1799441102"},{"seq_region_name":"7","id":"rs1799441217","clinical_significance":[],"end":140600407,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140600407,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["T","A"],"end":140600408,"feature_type":"variation","strand":1,"source":"dbSNP","start":140600408,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130682711"},{"seq_region_name":"7","id":"rs1799441337","clinical_significance":[],"strand":1,"feature_type":"variation","end":140600411,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140600411,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1332778038","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140600412,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140600412,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140600413,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140600413,"seq_region_name":"7","id":"rs1799441566","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563169287","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600417,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140600417},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140600420,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140600420,"source":"dbSNP","seq_region_name":"7","id":"rs1044775912","clinical_significance":[]},{"seq_region_name":"7","id":"rs746123726","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140600421,"source":"dbSNP","strand":1,"feature_type":"variation","end":140600421,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1799442079","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140600421,"source":"dbSNP","strand":1,"feature_type":"variation","end":140600424,"alleles":["GGGG","GGG"]},{"source":"dbSNP","start":140600423,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140600423,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1394445831"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600424,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140600424,"clinical_significance":[],"id":"rs965362716","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1585729599","seq_region_name":"7","alleles":["T","C","G"],"end":140600425,"feature_type":"variation","strand":1,"source":"dbSNP","start":140600425,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799442641","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600435,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140600435},{"start":140600441,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140600441,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799442789","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1383620464","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600445,"feature_type":"variation","strand":1,"end":140600445,"alleles":["G","A","T"]},{"seq_region_name":"7","id":"rs1799443048","clinical_significance":[],"start":140600450,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140600450,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1585729627","seq_region_name":"7","source":"dbSNP","start":140600452,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140600452,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600460,"feature_type":"variation","strand":1,"end":140600460,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1440534748"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140600464,"source":"dbSNP","strand":1,"feature_type":"variation","end":140600464,"alleles":["A","G"],"seq_region_name":"7","id":"rs1005814780","clinical_significance":[]},{"alleles":["G","T"],"end":140600466,"feature_type":"variation","strand":1,"source":"dbSNP","start":140600466,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799443519"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600467,"feature_type":"variation","strand":1,"end":140600467,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799443624"},{"clinical_significance":[],"id":"rs1799443764","seq_region_name":"7","alleles":["G","T"],"end":140600469,"feature_type":"variation","strand":1,"source":"dbSNP","start":140600469,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1037338386","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140600472,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140600472},{"seq_region_name":"7","id":"rs1799444008","clinical_significance":[],"end":140600475,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140600475,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140600477,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140600477,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799444134","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140600484,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140600484,"source":"dbSNP","seq_region_name":"7","id":"rs975439828","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140600488,"alleles":["CC","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600487,"clinical_significance":[],"id":"rs1799444403","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140600488,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140600488,"source":"dbSNP","id":"rs183345383","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs186590199","source":"dbSNP","start":140600491,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140600491,"alleles":["G","A","C"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140600496,"source":"dbSNP","strand":1,"feature_type":"variation","end":140600496,"alleles":["T","C"],"seq_region_name":"7","id":"rs1563169327","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600502,"feature_type":"variation","strand":1,"end":140600502,"alleles":["A","G"],"clinical_significance":[],"id":"rs1268612459","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799445055","clinical_significance":[],"alleles":["C","T"],"end":140600503,"strand":1,"feature_type":"variation","start":140600503,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1799445161","clinical_significance":[],"end":140600506,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140600506,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1212021815","seq_region_name":"7","feature_type":"variation","strand":1,"end":140600509,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600509},{"start":140600516,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140600516,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1398367658","clinical_significance":[]},{"seq_region_name":"7","id":"rs969013250","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140600517,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140600517},{"seq_region_name":"7","id":"rs1244866903","clinical_significance":[],"start":140600518,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140600518,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1353945678","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140600524,"source":"dbSNP","strand":1,"feature_type":"variation","end":140600524,"alleles":["G","A"]},{"start":140600529,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140600529,"alleles":["T","G"],"strand":1,"feature_type":"variation","id":"rs1799445904","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140600535,"source":"dbSNP","strand":1,"feature_type":"variation","end":140600535,"alleles":["T","C"],"seq_region_name":"7","id":"rs1799446013","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140600536,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600536,"clinical_significance":[],"seq_region_name":"7","id":"rs753370356"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140600544,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140600544,"seq_region_name":"7","id":"rs1310869313","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs993425228","end":140600552,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140600552,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799446480","source":"dbSNP","start":140600557,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140600557,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140600559,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600559,"clinical_significance":[],"id":"rs1441753949","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1324049161","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600560,"feature_type":"variation","strand":1,"end":140600560,"alleles":["G","A"]},{"clinical_significance":[],"id":"rs1388442002","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140600562,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600562},{"seq_region_name":"7","id":"rs78818827","clinical_significance":[],"start":140600566,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140600566,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1799447145","clinical_significance":[],"end":140600573,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140600573,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799447268","source":"dbSNP","start":140600575,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140600575,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1302275835","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600578,"feature_type":"variation","strand":1,"end":140600578,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs924809705","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140600580,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140600580,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130683029","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600585,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140600585},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140600587,"source":"dbSNP","strand":1,"feature_type":"variation","end":140600587,"alleles":["A","C"],"seq_region_name":"7","id":"rs1381098209","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600596,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140600596,"clinical_significance":[],"id":"rs1156915041","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600597,"feature_type":"variation","strand":1,"end":140600597,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799447851"},{"clinical_significance":[],"id":"rs1469642246","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600599,"feature_type":"variation","strand":1,"end":140600599,"alleles":["T","C"]},{"start":140600603,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140600603,"alleles":["A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585729835","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600605,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140600605,"clinical_significance":[],"id":"rs566193097","seq_region_name":"7"},{"id":"rs1799448338","seq_region_name":"7","clinical_significance":[],"start":140600608,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140600608,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1292569113","clinical_significance":[],"alleles":["T","A"],"end":140600611,"strand":1,"feature_type":"variation","start":140600611,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600612,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140600612,"clinical_significance":[],"seq_region_name":"7","id":"rs1799448599"},{"seq_region_name":"7","id":"rs935034182","clinical_significance":[],"end":140600617,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140600617,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1268686088","source":"dbSNP","start":140600618,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140600618,"feature_type":"variation","strand":1},{"end":140600619,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140600619,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs954554216","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","T"],"end":140600625,"strand":1,"feature_type":"variation","start":140600625,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1488432139","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600627,"feature_type":"variation","strand":1,"end":140600627,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799449188"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140600635,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140600635,"seq_region_name":"7","id":"rs1799449311","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140600637,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140600637,"source":"dbSNP","seq_region_name":"7","id":"rs1799449432","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1007827254","source":"dbSNP","start":140600639,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140600639,"alleles":["C","T"],"feature_type":"variation","strand":1},{"alleles":["G","A","T"],"end":140600640,"feature_type":"variation","strand":1,"source":"dbSNP","start":140600640,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1052133903"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1018346269","alleles":["G","A"],"end":140600641,"feature_type":"variation","strand":1,"source":"dbSNP","start":140600641,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1318584593","feature_type":"variation","strand":1,"end":140600646,"alleles":["AG","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600645},{"end":140600646,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140600646,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799450036"},{"source":"dbSNP","start":140600647,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140600647,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799450146"},{"seq_region_name":"7","id":"rs1585729934","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140600662,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140600662},{"start":140600663,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140600663,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799450374","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585729950","clinical_significance":[],"start":140600665,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140600665,"alleles":["T","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1799450643","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140600669,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140600669},{"clinical_significance":[],"id":"rs1799450760","seq_region_name":"7","source":"dbSNP","start":140600670,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140600670,"alleles":["A","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1274911012","clinical_significance":[],"end":140600673,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140600673,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1799450990","clinical_significance":[],"start":140600676,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140600676,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs191905745","seq_region_name":"7","source":"dbSNP","start":140600678,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G","T"],"end":140600678,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1799451297","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140600679,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140600679,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600683,"feature_type":"variation","strand":1,"end":140600683,"alleles":["G","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs979390377"},{"feature_type":"variation","strand":1,"end":140600684,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600684,"clinical_significance":[],"seq_region_name":"7","id":"rs1585729986"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140600699,"source":"dbSNP","strand":1,"feature_type":"variation","end":140600699,"alleles":["T","C"],"seq_region_name":"7","id":"rs1343528365","clinical_significance":[]},{"source":"dbSNP","start":140600700,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AGGAGG","AGG"],"end":140600705,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799451772"},{"seq_region_name":"7","id":"rs1799451893","clinical_significance":[],"start":140600704,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140600704,"strand":1,"feature_type":"variation"},{"end":140600710,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140600710,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1282429153","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","A"],"end":140600711,"strand":1,"feature_type":"variation","start":140600711,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1799452103","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","G"],"end":140600713,"feature_type":"variation","strand":1,"source":"dbSNP","start":140600713,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1400328226"},{"feature_type":"variation","strand":1,"end":140600714,"alleles":["T","C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600714,"clinical_significance":[],"id":"rs925274815","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140600721,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600721,"clinical_significance":[],"seq_region_name":"7","id":"rs1799452514"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140600726,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600726,"clinical_significance":[],"seq_region_name":"7","id":"rs956958620"},{"strand":1,"feature_type":"variation","end":140600729,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140600729,"source":"dbSNP","seq_region_name":"7","id":"rs949045989","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1255681454","alleles":["T","C"],"end":140600733,"feature_type":"variation","strand":1,"source":"dbSNP","start":140600733,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600734,"feature_type":"variation","strand":1,"end":140600734,"alleles":["G","C"],"clinical_significance":[],"id":"rs1799452922","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140600737,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140600737,"source":"dbSNP","seq_region_name":"7","id":"rs574417544","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799453210","clinical_significance":[],"start":140600738,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140600738,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1325504077","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600739,"feature_type":"variation","strand":1,"end":140600739,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799453470","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140600741,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600741},{"clinical_significance":[],"seq_region_name":"7","id":"rs1468739945","end":140600742,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140600742,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["G","C"],"end":140600749,"feature_type":"variation","strand":1,"source":"dbSNP","start":140600749,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1429153929","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600750,"feature_type":"variation","strand":1,"end":140600750,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs769782986"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600751,"feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140600751,"clinical_significance":[],"id":"rs1238370094","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600753,"feature_type":"variation","strand":1,"end":140600753,"alleles":["T","-"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799454184"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140600765,"source":"dbSNP","strand":1,"feature_type":"variation","end":140600765,"alleles":["C","T"],"seq_region_name":"7","id":"rs905095091","clinical_significance":[]},{"clinical_significance":[],"id":"rs1585730133","seq_region_name":"7","end":140600769,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140600769,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600775,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140600775,"clinical_significance":[],"seq_region_name":"7","id":"rs1799454548"},{"seq_region_name":"7","id":"rs1240714020","clinical_significance":[],"alleles":["C","T"],"end":140600786,"strand":1,"feature_type":"variation","start":140600786,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585730153","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600788,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140600788},{"clinical_significance":[],"id":"rs995449901","seq_region_name":"7","alleles":["C","G"],"end":140600789,"feature_type":"variation","strand":1,"source":"dbSNP","start":140600789,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140600790,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140600790,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799455111"},{"seq_region_name":"7","id":"rs1446042480","clinical_significance":[],"end":140600791,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140600791,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140600806,"source":"dbSNP","strand":1,"feature_type":"variation","end":140600806,"alleles":["T","C"],"id":"rs2130683445","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600811,"feature_type":"variation","strand":1,"end":140600811,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs918189404"},{"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140600821,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140600821,"source":"dbSNP","seq_region_name":"7","id":"rs1278754758","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799455648","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140600823,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600823},{"seq_region_name":"7","id":"rs1799455790","clinical_significance":[],"alleles":["A","G","T"],"end":140600829,"strand":1,"feature_type":"variation","start":140600829,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1417756027","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140600830,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140600830},{"seq_region_name":"7","id":"rs1204969912","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140600838,"source":"dbSNP","strand":1,"feature_type":"variation","end":140600838,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1478471603","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140600845,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140600845},{"clinical_significance":[],"seq_region_name":"7","id":"rs116147619","end":140600846,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140600846,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["CACA","CA"],"end":140600853,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140600850,"source":"dbSNP","seq_region_name":"7","id":"rs1219019252","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140600852,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140600852,"source":"dbSNP","id":"rs1421587604","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1268188449","clinical_significance":[],"start":140600860,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140600860,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140600867,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140600867,"source":"dbSNP","seq_region_name":"7","id":"rs1799456989","clinical_significance":[]},{"end":140600868,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140600868,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs1799457093","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140600869,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140600869,"source":"dbSNP","seq_region_name":"7","id":"rs1563169548","clinical_significance":[]},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600870,"feature_type":"variation","strand":1,"end":140600870,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799457319"},{"clinical_significance":[],"id":"rs1585730289","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140600873,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600873},{"seq_region_name":"7","id":"rs886950074","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140600874,"source":"dbSNP","strand":1,"feature_type":"variation","end":140600874,"alleles":["A","G"]},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140600875,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140600875,"seq_region_name":"7","id":"rs1341262830","clinical_significance":[]},{"end":140600876,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140600876,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs1336281349","clinical_significance":[]},{"end":140600878,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140600878,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs1450478824","clinical_significance":[]},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600879,"feature_type":"variation","strand":1,"end":140600879,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799458009"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799458142","feature_type":"variation","strand":1,"alleles":["TGTGT","TGT"],"end":140600896,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600892},{"source":"dbSNP","start":140600896,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140600896,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130683610"},{"source":"dbSNP","start":140600896,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140600903,"alleles":["TTATTTTA","TTA"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1004486594"},{"alleles":["T","C"],"end":140600897,"strand":1,"feature_type":"variation","start":140600897,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs1799458393","clinical_significance":[]},{"id":"rs1335145440","seq_region_name":"7","clinical_significance":[],"start":140600899,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["T","C"],"end":140600899,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140600901,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600901,"clinical_significance":[],"id":"rs139225037","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1417875266","clinical_significance":[],"end":140600905,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140600905,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"seq_region_name":"7","id":"rs965476490","clinical_significance":[],"alleles":["G","A"],"end":140600906,"strand":1,"feature_type":"variation","start":140600906,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"alleles":["T","C"],"end":140600908,"feature_type":"variation","strand":1,"source":"dbSNP","start":140600908,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1474893778"},{"clinical_significance":[],"seq_region_name":"7","id":"rs527556700","source":"dbSNP","start":140600909,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140600909,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs766195971","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600918,"feature_type":"variation","strand":1,"end":140600918,"alleles":["T","A"]},{"feature_type":"variation","strand":1,"alleles":["CACA","CA"],"end":140600922,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600919,"clinical_significance":[],"seq_region_name":"7","id":"rs1459538913"},{"seq_region_name":"7","id":"rs1241987324","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140600922,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140600922},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140600923,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600923,"clinical_significance":[],"seq_region_name":"7","id":"rs545610812"},{"id":"rs1799459665","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140600924,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140600924,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140600925,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140600925,"source":"dbSNP","seq_region_name":"7","id":"rs1799459787","clinical_significance":[]},{"source":"dbSNP","start":140600926,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140600926,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1309166188"},{"feature_type":"variation","strand":1,"end":140600927,"alleles":["G","A","C"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600927,"clinical_significance":[],"seq_region_name":"7","id":"rs183064863"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140600932,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600932,"clinical_significance":[],"seq_region_name":"7","id":"rs897481870"},{"source":"dbSNP","start":140600933,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140600933,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1357350283"},{"end":140600934,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140600934,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799460443"},{"source":"dbSNP","start":140600939,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140600939,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs993598480"},{"clinical_significance":[],"id":"rs1317356237","seq_region_name":"7","end":140600940,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140600940,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"alleles":["A","G"],"end":140600948,"feature_type":"variation","strand":1,"source":"dbSNP","start":140600948,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799460865"},{"strand":1,"feature_type":"variation","end":140600950,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140600950,"source":"dbSNP","id":"rs531383393","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799461131","clinical_significance":[],"alleles":["G","A"],"end":140600956,"strand":1,"feature_type":"variation","start":140600956,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"start":140600958,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["G","A"],"end":140600958,"strand":1,"feature_type":"variation","id":"rs1799461238","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1382199521","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140600963,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140600963},{"clinical_significance":[],"seq_region_name":"7","id":"rs550296550","source":"dbSNP","start":140600964,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140600964,"feature_type":"variation","strand":1},{"end":140600966,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140600966,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799461651"},{"seq_region_name":"7","id":"rs1353221525","clinical_significance":[],"strand":1,"feature_type":"variation","end":140600967,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140600967,"source":"dbSNP"},{"clinical_significance":[],"id":"rs187937244","seq_region_name":"7","alleles":["G","A","C"],"end":140600968,"feature_type":"variation","strand":1,"source":"dbSNP","start":140600968,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1051668998","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140600969,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140600969},{"clinical_significance":[],"seq_region_name":"7","id":"rs1414070015","source":"dbSNP","start":140600970,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140600970,"feature_type":"variation","strand":1},{"start":140600972,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["A","G"],"end":140600972,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799462323","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140600975,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600975,"clinical_significance":[],"seq_region_name":"7","id":"rs1165160179"},{"source":"dbSNP","start":140600979,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140600984,"alleles":["TTGTTT","TT"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1442383599","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140600981,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140600981,"clinical_significance":[],"id":"rs1799462655","seq_region_name":"7"},{"alleles":["G","A"],"end":140600988,"strand":1,"feature_type":"variation","start":140600988,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs1799462763","clinical_significance":[]},{"id":"rs890385426","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140600991,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140600991,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140600993,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["ATAGATAGA","ATAGA"],"end":140601001,"seq_region_name":"7","id":"rs1178685286","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1280269916","end":140600994,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140600994,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1231056282","clinical_significance":[],"start":140600997,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["A","G"],"end":140600997,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140600998,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140600998,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1203577706","seq_region_name":"7"},{"source":"dbSNP","start":140601000,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140601000,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799463489"},{"clinical_significance":[],"seq_region_name":"7","id":"rs568452978","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140601004,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601004},{"seq_region_name":"7","id":"rs1007363995","clinical_significance":[],"end":140601005,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140601005,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799463847","alleles":["T","C"],"end":140601008,"feature_type":"variation","strand":1,"source":"dbSNP","start":140601008,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"alleles":["A","C"],"end":140601009,"feature_type":"variation","strand":1,"source":"dbSNP","start":140601009,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs191238695"},{"strand":1,"feature_type":"variation","end":140601010,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140601010,"source":"dbSNP","seq_region_name":"7","id":"rs1799464046","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799464164","end":140601016,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140601016,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs745590499","clinical_significance":[],"alleles":["TTT","TT"],"end":140601023,"strand":1,"feature_type":"variation","start":140601021,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140601028,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140601028,"seq_region_name":"7","id":"rs1799464423","clinical_significance":[]},{"id":"rs1209170065","seq_region_name":"7","clinical_significance":[],"end":140601029,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140601029,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"seq_region_name":"7","id":"rs1799464676","clinical_significance":[],"end":140601031,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140601031,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"end":140601034,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140601034,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs765118909"},{"seq_region_name":"7","id":"rs992987054","clinical_significance":[],"start":140601035,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140601035,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs964083304","seq_region_name":"7","alleles":["C","G","T"],"end":140601036,"feature_type":"variation","strand":1,"source":"dbSNP","start":140601036,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs114772747","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140601037,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601037},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799465388","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140601038,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601038},{"source":"dbSNP","start":140601047,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140601047,"alleles":["T","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799465510","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140601048,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140601048,"seq_region_name":"7","id":"rs1799465690","clinical_significance":[]},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601051,"feature_type":"variation","strand":1,"end":140601051,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799465804"},{"alleles":["C","G"],"end":140601052,"feature_type":"variation","strand":1,"source":"dbSNP","start":140601052,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799465932"},{"clinical_significance":[],"id":"rs1225486798","seq_region_name":"7","feature_type":"variation","strand":1,"end":140601055,"alleles":["T","A","G"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601055},{"alleles":["TAGTTAG","TAG"],"end":140601064,"feature_type":"variation","strand":1,"source":"dbSNP","start":140601058,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1279415324"},{"clinical_significance":[],"seq_region_name":"7","id":"rs949157597","source":"dbSNP","start":140601059,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140601059,"alleles":["A","G"],"feature_type":"variation","strand":1},{"id":"rs1799466315","seq_region_name":"7","clinical_significance":[],"start":140601060,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["G","-"],"end":140601060,"strand":1,"feature_type":"variation"},{"end":140601066,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140601066,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1032459204"},{"start":140601069,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140601069,"alleles":["G","A","C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs375747708","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799466738","clinical_significance":[],"start":140601070,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["-","TTA"],"end":140601069,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140601072,"source":"dbSNP","strand":1,"feature_type":"variation","end":140601072,"alleles":["T","A","C"],"id":"rs1799466863","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140601079,"source":"dbSNP","strand":1,"feature_type":"variation","end":140601079,"alleles":["T","C"],"seq_region_name":"7","id":"rs1422409557","clinical_significance":[]},{"seq_region_name":"7","id":"rs988567613","clinical_significance":[],"strand":1,"feature_type":"variation","end":140601082,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140601082,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140601083,"source":"dbSNP","strand":1,"feature_type":"variation","end":140601083,"alleles":["A","G"],"seq_region_name":"7","id":"rs1364524565","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140601084,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140601084,"source":"dbSNP","seq_region_name":"7","id":"rs1158749883","clinical_significance":[]},{"id":"rs1420294577","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140601086,"source":"dbSNP","strand":1,"feature_type":"variation","end":140601086,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1799467796","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140601088,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140601088},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799467909","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140601090,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601090},{"seq_region_name":"7","id":"rs1799468003","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140601094,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140601094,"source":"dbSNP"},{"alleles":["C","T"],"end":140601099,"strand":1,"feature_type":"variation","start":140601099,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs566397452","clinical_significance":[]},{"seq_region_name":"7","id":"rs931185280","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140601100,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140601100},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601102,"feature_type":"variation","strand":1,"end":140601102,"alleles":["A","G"],"clinical_significance":[],"id":"rs2130684108","seq_region_name":"7"},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601104,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140601104,"clinical_significance":[],"seq_region_name":"7","id":"rs1025197094"},{"clinical_significance":[],"id":"rs142511880","seq_region_name":"7","alleles":["T","C"],"end":140601109,"feature_type":"variation","strand":1,"source":"dbSNP","start":140601109,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"end":140601111,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140601111,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799468771","seq_region_name":"7"},{"id":"rs558472007","seq_region_name":"7","clinical_significance":[],"end":140601112,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140601112,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140601117,"source":"dbSNP","strand":1,"feature_type":"variation","end":140601117,"alleles":["C","T"],"seq_region_name":"7","id":"rs1799469150","clinical_significance":[]},{"end":140601123,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140601123,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs1004031048","clinical_significance":[]},{"start":140601124,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["T","C"],"end":140601124,"strand":1,"feature_type":"variation","id":"rs1040917025","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","G","T"],"end":140601135,"feature_type":"variation","strand":1,"source":"dbSNP","start":140601135,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1286933202"},{"strand":1,"feature_type":"variation","end":140601139,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140601139,"source":"dbSNP","seq_region_name":"7","id":"rs1799469815","clinical_significance":[]},{"source":"dbSNP","start":140601145,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140601145,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs980866422"},{"end":140601150,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140601150,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs901227137","clinical_significance":[]},{"end":140601153,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140601153,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130684179"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140601156,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601156,"clinical_significance":[],"id":"rs1360947773","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1283635874","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140601159,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601159},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799470386","end":140601162,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140601162,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140601175,"alleles":["G","-"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140601175,"source":"dbSNP","seq_region_name":"7","id":"rs1220365423","clinical_significance":[]},{"end":140601178,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140601178,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs73500426","clinical_significance":[]},{"id":"rs1799470744","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140601180,"source":"dbSNP","strand":1,"feature_type":"variation","end":140601180,"alleles":["T","C"]},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140601182,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601182,"clinical_significance":[],"seq_region_name":"7","id":"rs1296302456"},{"end":140601197,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140601197,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs146003431"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140601207,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140601207,"source":"dbSNP","seq_region_name":"7","id":"rs1799471127","clinical_significance":[]},{"start":140601209,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140601209,"alleles":["A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs556235388","clinical_significance":[]},{"start":140601210,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["C","T"],"end":140601210,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs548843959","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140601220,"alleles":["A","G"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601220,"clinical_significance":[],"seq_region_name":"7","id":"rs1799471554"},{"source":"dbSNP","start":140601221,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140601221,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1436554661","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140601223,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140601223,"source":"dbSNP","seq_region_name":"7","id":"rs1799471837","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140601224,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140601224,"source":"dbSNP","seq_region_name":"7","id":"rs2130684281","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799471941","source":"dbSNP","start":140601225,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140601225,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs551377384","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140601229,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140601229},{"seq_region_name":"7","id":"rs10081295","clinical_significance":[],"start":140601233,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140601233,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs139968401","source":"dbSNP","start":140601235,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140601235,"feature_type":"variation","strand":1},{"id":"rs1342974160","seq_region_name":"7","clinical_significance":[],"end":140601239,"alleles":["T","C","G"],"strand":1,"feature_type":"variation","start":140601239,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"strand":1,"feature_type":"variation","end":140601252,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140601252,"source":"dbSNP","seq_region_name":"7","id":"rs745595515","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799472579","clinical_significance":[],"start":140601254,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140601254,"alleles":["A","G","T"],"strand":1,"feature_type":"variation"},{"id":"rs1157693015","seq_region_name":"7","clinical_significance":[],"start":140601255,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140601255,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601258,"feature_type":"variation","strand":1,"end":140601258,"alleles":["T","C"],"clinical_significance":[],"id":"rs1414999400","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1031911846","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140601263,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140601263},{"start":140601267,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["C","T"],"end":140601267,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs149758275","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799473173","clinical_significance":[],"start":140601270,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["T","C"],"end":140601270,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140601275,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601275,"clinical_significance":[],"seq_region_name":"7","id":"rs992934792"},{"source":"dbSNP","start":140601280,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","end":140601280,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799473408"},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140601300,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140601300,"seq_region_name":"7","id":"rs1024441315","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799473677","seq_region_name":"7","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601301,"feature_type":"variation","strand":1,"end":140601301,"alleles":["T","C"]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140601305,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601305,"clinical_significance":[],"seq_region_name":"7","id":"rs970417890"},{"seq_region_name":"7","id":"rs1485004278","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140601310,"source":"dbSNP","strand":1,"feature_type":"variation","end":140601310,"alleles":["A","C"]},{"clinical_significance":[],"id":"rs1799474027","seq_region_name":"7","feature_type":"variation","strand":1,"end":140601312,"alleles":["A","G"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601312},{"id":"rs1799474130","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140601321,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140601321},{"alleles":["A","C"],"end":140601324,"feature_type":"variation","strand":1,"source":"dbSNP","start":140601324,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799474250"},{"seq_region_name":"7","id":"rs2130684440","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140601326,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140601326},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140601332,"source":"dbSNP","strand":1,"feature_type":"variation","end":140601332,"alleles":["C","T"],"seq_region_name":"7","id":"rs752305987","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140601333,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140601333,"seq_region_name":"7","id":"rs1279993990","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799474669","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601333,"feature_type":"variation","strand":1,"end":140601334,"alleles":["GG","G"]},{"feature_type":"variation","strand":1,"end":140601338,"alleles":["T","C"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601338,"clinical_significance":[],"seq_region_name":"7","id":"rs1799474784"},{"seq_region_name":"7","id":"rs1326314996","clinical_significance":[],"end":140601339,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140601339,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs202205219","alleles":["A","G"],"end":140601340,"feature_type":"variation","strand":1,"source":"dbSNP","start":140601340,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1799475180","clinical_significance":[],"end":140601347,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140601347,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"start":140601348,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","alleles":["C","T"],"end":140601348,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1219305505","clinical_significance":[]},{"seq_region_name":"7","id":"rs930980619","clinical_significance":[],"start":140601350,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140601350,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140601353,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140601353,"source":"dbSNP","seq_region_name":"7","id":"rs778791391","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1435547664","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601355,"feature_type":"variation","strand":1,"end":140601355,"alleles":["C","T"]},{"start":140601357,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140601357,"alleles":["G","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs748131673","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs759740833","end":140601363,"alleles":["GAGAGAG","GAGAG"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140601357,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs199746686","seq_region_name":"7","end":140601359,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140601359,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1298154818","alleles":["G","A","C"],"end":140601361,"feature_type":"variation","strand":1,"source":"dbSNP","start":140601361,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140601364,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601364,"clinical_significance":[],"seq_region_name":"7","id":"rs1347366032"},{"clinical_significance":[],"id":"rs1429012248","seq_region_name":"7","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601365,"feature_type":"variation","strand":1,"end":140601365,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs908431715","clinical_significance":[],"alleles":["G","A"],"end":140601368,"strand":1,"feature_type":"variation","start":140601368,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"start":140601369,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140601369,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585731309","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs773020773","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140601371,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601371},{"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601372,"feature_type":"variation","strand":1,"end":140601372,"alleles":["C","T"],"clinical_significance":[],"id":"rs760319038","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs770478576","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601373,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140601373},{"start":140601374,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","end":140601374,"alleles":["A","G"],"strand":1,"feature_type":"variation","id":"rs776413227","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs765498393","feature_type":"variation","strand":1,"alleles":["CACTCTGCCTGGCCACACC","C"],"end":140601393,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601375},{"seq_region_name":"7","id":"rs1479870157","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140601376,"source":"dbSNP","strand":1,"feature_type":"variation","end":140601376,"alleles":["A","C","G"]},{"alleles":["CTCT","CT"],"end":140601380,"feature_type":"variation","strand":1,"source":"dbSNP","start":140601377,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs752713320"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799477652","consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601378,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140601378},{"feature_type":"variation","strand":1,"end":140601383,"alleles":["C","T"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601383,"clinical_significance":[],"id":"rs758937926","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140601384,"alleles":["T","C"],"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601384,"clinical_significance":[],"id":"rs2130684633","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["G","C","T"],"end":140601386,"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140601386,"source":"dbSNP","seq_region_name":"7","id":"rs370836687","clinical_significance":[]},{"seq_region_name":"7","id":"rs1469215420","clinical_significance":[],"alleles":["C","T"],"end":140601388,"strand":1,"feature_type":"variation","start":140601388,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant"},{"seq_region_name":"7","id":"rs531576188","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","start":140601392,"source":"dbSNP","strand":1,"feature_type":"variation","end":140601392,"alleles":["C","T"]},{"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140601393,"consequence_type":"3_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601393,"clinical_significance":[],"seq_region_name":"7","id":"rs374099434"},{"alleles":["G","A"],"end":140601394,"strand":1,"feature_type":"variation","start":140601394,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"3_prime_UTR_variant","seq_region_name":"7","id":"rs764489237","clinical_significance":[]},{"alleles":["GG","G"],"end":140601395,"feature_type":"variation","strand":1,"source":"dbSNP","start":140601394,"consequence_type":"splice_region_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs758506656"},{"start":140601398,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_donor_5th_base_variant","end":140601398,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1448548708","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799478840","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140601400,"consequence_type":"stop_lost","assembly_name":"GRCh38","source":"dbSNP","start":140601400},{"feature_type":"variation","strand":1,"end":140601404,"alleles":["T","C"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601404,"clinical_significance":[],"id":"rs1167810914","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1213322421","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140601408,"source":"dbSNP","strand":1,"feature_type":"variation","end":140601408,"alleles":["G","T"]},{"seq_region_name":"7","id":"rs751880561","clinical_significance":[],"alleles":["C","G"],"end":140601415,"strand":1,"feature_type":"variation","start":140601415,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"end":140601418,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140601418,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs1394480151","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140601420,"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140601420,"source":"dbSNP","seq_region_name":"7","id":"rs757695883","clinical_significance":[]},{"start":140601429,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","alleles":["C","T"],"end":140601429,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs367947493","clinical_significance":[]},{"source":"dbSNP","start":140601430,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140601430,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1427356376"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140601431,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140601431,"source":"dbSNP","id":"rs750694634","seq_region_name":"7","clinical_significance":["uncertain significance"]},{"start":140601432,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","end":140601432,"alleles":["G","A","C","T"],"strand":1,"feature_type":"variation","id":"rs756164121","seq_region_name":"7","clinical_significance":[]},{"id":"rs780130207","seq_region_name":"7","clinical_significance":[],"start":140601433,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140601433,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140601435,"consequence_type":"stop_gained","assembly_name":"GRCh38","alleles":["C","T"],"end":140601435,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1563169980"},{"id":"rs2130684781","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140601436,"source":"dbSNP","strand":1,"feature_type":"variation","end":140601436,"alleles":["C","A"]},{"id":"rs1563169988","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"frameshift_variant","start":140601436,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CACA","CA"],"end":140601439},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140601438,"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140601438,"source":"dbSNP","seq_region_name":"7","id":"rs748035712","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140601439,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140601439,"seq_region_name":"7","id":"rs772000768","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140601440,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140601440,"source":"dbSNP","id":"rs182310674","seq_region_name":"7","clinical_significance":[]},{"end":140601444,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140601444,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","seq_region_name":"7","id":"rs1407363517","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799481413","clinical_significance":[],"end":140601446,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140601446,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1301817270","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601448,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140601448},{"id":"rs1799481705","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140601452,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140601452},{"seq_region_name":"7","id":"rs1328894168","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140601455,"source":"dbSNP","strand":1,"feature_type":"variation","end":140601455,"alleles":["A","C"]},{"end":140601456,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140601456,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","seq_region_name":"7","id":"rs770800056","clinical_significance":[]},{"end":140601457,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140601457,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs776126618","clinical_significance":["uncertain significance"]},{"seq_region_name":"7","id":"rs1799482309","clinical_significance":[],"strand":1,"feature_type":"variation","end":140601460,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140601460,"source":"dbSNP"},{"start":140601461,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140601461,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799482442","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140601462,"alleles":["T","C","G"],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140601462,"source":"dbSNP","seq_region_name":"7","id":"rs1585731738","clinical_significance":[]},{"seq_region_name":"7","id":"rs759258670","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140601463,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C","T"],"end":140601463},{"clinical_significance":[],"id":"rs1305412652","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["GGGGGAGAGGAGGGCAGAGGCGGGGGAG","GGGGGAG"],"end":140601490,"consequence_type":"inframe_deletion","assembly_name":"GRCh38","source":"dbSNP","start":140601463},{"clinical_significance":[],"seq_region_name":"7","id":"rs1384434142","source":"dbSNP","start":140601464,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140601464,"feature_type":"variation","strand":1},{"end":140601465,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140601465,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","id":"rs1237689876","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1334095449","source":"dbSNP","start":140601468,"consequence_type":"frameshift_variant","assembly_name":"GRCh38","end":140601468,"alleles":["A","-"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140601468,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140601468,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799483430"},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140601472,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140601472,"source":"dbSNP","id":"rs1799483675","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs767414700","source":"dbSNP","start":140601472,"consequence_type":"inframe_deletion","assembly_name":"GRCh38","alleles":["GAGGGCAGAGGCGGGGGAGGTAGAGAGGGCAGAGG","GAGGGCAGAGG"],"end":140601506,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799483956","source":"dbSNP","start":140601479,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140601479,"feature_type":"variation","strand":1},{"start":140601480,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","alleles":["A","G"],"end":140601480,"strand":1,"feature_type":"variation","id":"rs1799484184","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs769392021","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601482,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140601482},{"seq_region_name":"7","id":"rs775147801","clinical_significance":[],"start":140601483,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","alleles":["C","A","T"],"end":140601483,"strand":1,"feature_type":"variation"},{"alleles":["G","A","C"],"end":140601484,"feature_type":"variation","strand":1,"source":"dbSNP","start":140601484,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs763493748","seq_region_name":"7"},{"start":140601486,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","alleles":["G","A"],"end":140601486,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs374414521","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs367593121","alleles":["G","A"],"end":140601488,"feature_type":"variation","strand":1,"source":"dbSNP","start":140601488,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs752171246","clinical_significance":[],"start":140601489,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","alleles":["A","G","T"],"end":140601489,"strand":1,"feature_type":"variation"},{"id":"rs1799485914","seq_region_name":"7","clinical_significance":[],"alleles":["GG","G"],"end":140601491,"strand":1,"feature_type":"variation","start":140601490,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"frameshift_variant"},{"clinical_significance":[],"id":"rs762048904","seq_region_name":"7","consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601492,"feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140601492},{"alleles":["TAGAGA","-"],"end":140601497,"strand":1,"feature_type":"variation","start":140601492,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"inframe_deletion","id":"rs1234821868","seq_region_name":"7","clinical_significance":[]},{"id":"rs372251918","seq_region_name":"7","clinical_significance":[],"start":140601496,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["G","A","C"],"end":140601496,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1799486595","clinical_significance":[],"alleles":["G","T"],"end":140601500,"strand":1,"feature_type":"variation","start":140601500,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1386303435","source":"dbSNP","start":140601502,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["A","G","T"],"end":140601502,"feature_type":"variation","strand":1},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601506,"feature_type":"variation","strand":1,"end":140601506,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1426914960"},{"end":140601508,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140601508,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs374255633"},{"source":"dbSNP","start":140601513,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","end":140601513,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs201648870"},{"end":140601517,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140601517,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","id":"rs368471013","seq_region_name":"7","clinical_significance":["uncertain significance"]},{"source":"dbSNP","start":140601520,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140601520,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs777540395","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130685142","end":140601525,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140601525,"consequence_type":"synonymous_variant","assembly_name":"GRCh38"},{"id":"rs1438918239","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140601526,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140601526,"source":"dbSNP"},{"id":"rs371899909","seq_region_name":"7","clinical_significance":[],"start":140601528,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","end":140601528,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140601529,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140601529,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799491952"},{"clinical_significance":["uncertain significance"],"id":"rs2486260290","seq_region_name":"7","alleles":["T","C"],"end":140601530,"feature_type":"variation","strand":1,"source":"ClinVar","start":140601530,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799492179","alleles":["A","C"],"end":140601532,"feature_type":"variation","strand":1,"source":"dbSNP","start":140601532,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs2130685186","clinical_significance":[],"strand":1,"feature_type":"variation","end":140601533,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140601533,"source":"dbSNP"},{"seq_region_name":"7","id":"rs375363340","clinical_significance":[],"start":140601536,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140601536,"alleles":["C","G","T"],"strand":1,"feature_type":"variation"},{"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601537,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140601537,"clinical_significance":[],"seq_region_name":"7","id":"rs781077093"},{"start":140601539,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140601539,"alleles":["T","C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs745450247","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140601541,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601541,"clinical_significance":[],"id":"rs1247845867","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1263626915","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140601544,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140601544,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1355474396","clinical_significance":[],"end":140601545,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140601545,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"seq_region_name":"7","id":"rs145700393","clinical_significance":[],"strand":1,"feature_type":"variation","end":140601549,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140601549,"source":"dbSNP"},{"start":140601551,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140601551,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799494199","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1275279476","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140601554,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601554},{"seq_region_name":"7","id":"rs1361114760","clinical_significance":[],"alleles":["T","C"],"end":140601556,"strand":1,"feature_type":"variation","start":140601556,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"source":"dbSNP","start":140601557,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140601557,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":["uncertain significance"],"id":"rs748800834","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140601558,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140601558,"source":"dbSNP","seq_region_name":"7","id":"rs963495871","clinical_significance":[]},{"clinical_significance":[],"id":"rs768248304","seq_region_name":"7","end":140601559,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140601559,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1243937603","feature_type":"variation","strand":1,"end":140601560,"alleles":["C","G","T"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601560},{"id":"rs774695285","seq_region_name":"7","clinical_significance":[],"start":140601561,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","end":140601561,"alleles":["C","A","G","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1308982660","seq_region_name":"7","source":"dbSNP","start":140601563,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140601563,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1182064848","feature_type":"variation","strand":1,"end":140601568,"alleles":["C","G"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601568},{"seq_region_name":"7","id":"rs762403461","clinical_significance":[],"alleles":["C","T"],"end":140601569,"strand":1,"feature_type":"variation","start":140601569,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140601570,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140601570,"seq_region_name":"7","id":"rs371627954","clinical_significance":[]},{"alleles":["G","A","C"],"end":140601571,"strand":1,"feature_type":"variation","start":140601571,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","id":"rs866315552","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs773628121","clinical_significance":[],"start":140601574,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["T","C","G"],"end":140601574,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130685374","feature_type":"variation","strand":1,"end":140601575,"alleles":["G","A"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601575},{"clinical_significance":[],"id":"rs1398070242","seq_region_name":"7","end":140601578,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140601578,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1799498128","clinical_significance":[],"strand":1,"feature_type":"variation","end":140601579,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140601579,"source":"dbSNP"},{"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601582,"feature_type":"variation","strand":1,"alleles":["C","A","G","T"],"end":140601582,"clinical_significance":[],"seq_region_name":"7","id":"rs61737089"},{"end":140601583,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140601583,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs983775359","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799498577","seq_region_name":"7","source":"dbSNP","start":140601586,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140601586,"alleles":["C","G","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs368140148","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140601589,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601589},{"source":"dbSNP","start":140601590,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140601590,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":["uncertain significance"],"seq_region_name":"7","id":"rs755029421"},{"seq_region_name":"7","id":"rs765381926","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140601593,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140601593,"source":"dbSNP"},{"end":140601597,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140601597,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","seq_region_name":"7","id":"rs1339638016","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799499650","source":"dbSNP","start":140601601,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140601601,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140601602,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601602,"clinical_significance":[],"seq_region_name":"7","id":"rs751415526"},{"seq_region_name":"7","id":"rs757227434","clinical_significance":[],"alleles":["A","G"],"end":140601603,"strand":1,"feature_type":"variation","start":140601603,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799500379","source":"dbSNP","start":140601611,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140601611,"feature_type":"variation","strand":1},{"id":"rs200792236","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140601612,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140601612,"source":"dbSNP"},{"seq_region_name":"7","id":"rs537657395","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140601615,"source":"dbSNP","strand":1,"feature_type":"variation","end":140601615,"alleles":["G","A"]},{"feature_type":"variation","strand":1,"end":140601616,"alleles":["G","A"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601616,"clinical_significance":[],"seq_region_name":"7","id":"rs368696269"},{"seq_region_name":"7","id":"rs1198030115","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140601618,"source":"dbSNP","strand":1,"feature_type":"variation","end":140601618,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs745642049","end":140601623,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140601623,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs756037054","seq_region_name":"7","end":140601624,"alleles":["G","A","C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140601624,"consequence_type":"synonymous_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1198945681","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140601625,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601625},{"seq_region_name":"7","id":"rs779818540","clinical_significance":[],"end":140601626,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140601626,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140601627,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601627,"clinical_significance":[],"seq_region_name":"7","id":"rs1418981482"},{"source":"dbSNP","start":140601628,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140601628,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs748993429"},{"end":140601629,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140601629,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs1799502160","clinical_significance":[]},{"source":"dbSNP","start":140601630,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","end":140601630,"alleles":["A","C","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs768001423"},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140601631,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140601631,"seq_region_name":"7","id":"rs943048059","clinical_significance":["uncertain significance"]},{"alleles":["C","G","T"],"end":140601635,"feature_type":"variation","strand":1,"source":"dbSNP","start":140601635,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs748534835"},{"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601636,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140601636,"clinical_significance":[],"seq_region_name":"7","id":"rs1476568045"},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140601637,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140601637,"id":"rs1038953341","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs772645341","source":"dbSNP","start":140601640,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140601640,"alleles":["C","A","T"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140601641,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140601641,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1470784450","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1350848911","clinical_significance":[],"start":140601643,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["C","T"],"end":140601643,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140601645,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140601645,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs773775860","seq_region_name":"7"},{"seq_region_name":"7","id":"rs760998955","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140601648,"source":"dbSNP","strand":1,"feature_type":"variation","end":140601648,"alleles":["C","A"]},{"start":140601649,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["A","G"],"end":140601649,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1563170525","clinical_significance":[]},{"clinical_significance":[],"id":"rs766779073","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140601650,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601650},{"source":"dbSNP","start":140601651,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140601651,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"clinical_significance":["uncertain significance"],"seq_region_name":"7","id":"rs1297660931"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799504551","consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601654,"feature_type":"variation","strand":1,"end":140601654,"alleles":["C","T"]},{"source":"dbSNP","start":140601659,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140601659,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs555654400"},{"seq_region_name":"7","id":"rs1300248622","clinical_significance":["uncertain significance"],"alleles":["G","C","T"],"end":140601660,"strand":1,"feature_type":"variation","start":140601660,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs759788997","feature_type":"variation","strand":1,"end":140601661,"alleles":["C","T"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601661},{"clinical_significance":[],"seq_region_name":"7","id":"rs568165538","source":"dbSNP","start":140601664,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140601664,"alleles":["C","T"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140601665,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140601665,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs752837618"},{"seq_region_name":"7","id":"rs1325748197","clinical_significance":["uncertain significance"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140601671,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140601671},{"feature_type":"variation","strand":1,"end":140601673,"alleles":["G","A"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601673,"clinical_significance":[],"id":"rs866423658","seq_region_name":"7"},{"seq_region_name":"7","id":"rs758468568","clinical_significance":[],"strand":1,"feature_type":"variation","end":140601675,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140601675,"source":"dbSNP"},{"seq_region_name":"7","id":"rs767483104","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140601676,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140601676,"source":"dbSNP"},{"alleles":["C","T"],"end":140601679,"strand":1,"feature_type":"variation","start":140601679,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs935792240","clinical_significance":[]},{"end":140601680,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140601680,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs750423922"},{"seq_region_name":"7","id":"rs755946915","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140601681,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140601681},{"source":"dbSNP","start":140601682,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140601682,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1053371086"},{"seq_region_name":"7","id":"rs780014751","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140601684,"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140601684,"source":"dbSNP"},{"id":"rs757645835","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140601686,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140601686},{"seq_region_name":"7","id":"rs1010064300","clinical_significance":["uncertain significance"],"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140601689,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140601689,"source":"dbSNP"},{"start":140601698,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["C","T"],"end":140601698,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs754664075","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs200261624","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140601699,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601699},{"alleles":["C","T"],"end":140601701,"feature_type":"variation","strand":1,"source":"dbSNP","start":140601701,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs747679519"},{"alleles":["A","C"],"end":140601703,"feature_type":"variation","strand":1,"source":"dbSNP","start":140601703,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs200132556"},{"seq_region_name":"7","id":"rs1324627064","clinical_significance":[],"strand":1,"feature_type":"variation","end":140601707,"alleles":["G","C","T"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140601707,"source":"dbSNP"},{"seq_region_name":"7","id":"rs778233422","clinical_significance":["uncertain significance"],"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140601713,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140601713,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1315226113","seq_region_name":"7","end":140601714,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140601714,"consequence_type":"synonymous_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1299741755","clinical_significance":[],"alleles":["G","T"],"end":140601715,"strand":1,"feature_type":"variation","start":140601715,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"feature_type":"variation","strand":1,"end":140601719,"alleles":["G","C"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601719,"clinical_significance":[],"seq_region_name":"7","id":"rs1358391518"},{"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140601722,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601722,"clinical_significance":[],"seq_region_name":"7","id":"rs747536968"},{"clinical_significance":[],"id":"rs771246634","seq_region_name":"7","alleles":["G","A"],"end":140601726,"feature_type":"variation","strand":1,"source":"dbSNP","start":140601726,"consequence_type":"synonymous_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["CC","C"],"end":140601738,"assembly_name":"GRCh38","consequence_type":"frameshift_variant","start":140601737,"source":"dbSNP","seq_region_name":"7","id":"rs1347514028","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs188173983","consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601738,"feature_type":"variation","strand":1,"alleles":["C","A","G","T"],"end":140601738},{"end":140601739,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140601739,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs78836925"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1268626342","consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601741,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140601741},{"seq_region_name":"7","id":"rs775644497","clinical_significance":[],"start":140601742,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140601742,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs763055670","clinical_significance":[],"end":140601743,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140601743,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"seq_region_name":"7","id":"rs1284394822","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140601744,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140601744,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140601745,"source":"dbSNP","strand":1,"feature_type":"variation","end":140601745,"alleles":["T","C"],"seq_region_name":"7","id":"rs906148441","clinical_significance":[]},{"seq_region_name":"7","id":"rs764313653","clinical_significance":[],"start":140601747,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","alleles":["G","T"],"end":140601747,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs750333886","seq_region_name":"7","feature_type":"variation","strand":1,"end":140601749,"alleles":["C","A"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601749},{"start":140601750,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140601750,"alleles":["C","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1379581559","clinical_significance":[]},{"end":140601756,"alleles":["GG","GGG"],"strand":1,"feature_type":"variation","start":140601755,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"frameshift_variant","seq_region_name":"7","id":"rs1001686435","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140601756,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140601756,"seq_region_name":"7","id":"rs1799511023","clinical_significance":[]},{"start":140601757,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["C","T"],"end":140601757,"strand":1,"feature_type":"variation","id":"rs373569689","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140601758,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140601758,"source":"dbSNP","seq_region_name":"7","id":"rs1799511320","clinical_significance":[]},{"id":"rs766209410","seq_region_name":"7","clinical_significance":[],"end":140601761,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140601761,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"seq_region_name":"7","id":"rs753697413","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140601762,"source":"dbSNP","strand":1,"feature_type":"variation","end":140601762,"alleles":["T","G"]},{"seq_region_name":"7","id":"rs754785886","clinical_significance":[],"alleles":["T","G"],"end":140601763,"strand":1,"feature_type":"variation","start":140601763,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs963610364","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140601765,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601765},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601769,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140601769,"clinical_significance":["uncertain significance"],"seq_region_name":"7","id":"rs1321228886"},{"seq_region_name":"7","id":"rs983778089","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"frameshift_variant","start":140601769,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CCACTCCCGCCTCCCA","CCA"],"end":140601784},{"clinical_significance":[],"seq_region_name":"7","id":"rs1005714574","feature_type":"variation","strand":1,"end":140601775,"alleles":["C","T"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601775},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601776,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140601776,"clinical_significance":[],"seq_region_name":"7","id":"rs778598393"},{"alleles":["G","A","C"],"end":140601777,"strand":1,"feature_type":"variation","start":140601777,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","seq_region_name":"7","id":"rs192613819","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140601786,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140601786,"source":"dbSNP","id":"rs777296975","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","T"],"end":140601792,"strand":1,"feature_type":"variation","start":140601792,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","seq_region_name":"7","id":"rs1164168686","clinical_significance":[]},{"id":"rs1799513023","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140601796,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140601796},{"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601798,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140601798,"clinical_significance":[],"seq_region_name":"7","id":"rs1799513165"},{"alleles":["A","C"],"end":140601803,"strand":1,"feature_type":"variation","start":140601803,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs1351498232","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs747452713","alleles":["C","T"],"end":140601805,"feature_type":"variation","strand":1,"source":"dbSNP","start":140601805,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"end":140601806,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140601806,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1316343575"},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140601810,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140601810,"seq_region_name":"7","id":"rs1293084331","clinical_significance":[]},{"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601813,"feature_type":"variation","strand":1,"end":140601813,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1260016565"},{"seq_region_name":"7","id":"rs1407479494","clinical_significance":[],"strand":1,"feature_type":"variation","end":140601814,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140601814,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1374130475","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140601815,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601815},{"seq_region_name":"7","id":"rs370796734","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140601818,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140601818},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140601823,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140601823,"source":"dbSNP","seq_region_name":"7","id":"rs950949983","clinical_significance":[]},{"seq_region_name":"7","id":"rs1376664332","clinical_significance":[],"alleles":["A","T"],"end":140601825,"strand":1,"feature_type":"variation","start":140601825,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant"},{"id":"rs1799514708","seq_region_name":"7","clinical_significance":[],"start":140601828,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","end":140601828,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"alleles":["C","T"],"end":140601829,"feature_type":"variation","strand":1,"source":"dbSNP","start":140601829,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":["uncertain significance"],"seq_region_name":"7","id":"rs142818312"},{"feature_type":"variation","strand":1,"end":140601832,"alleles":["T","C"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601832,"clinical_significance":[],"seq_region_name":"7","id":"rs746242476"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799515102","alleles":["G","T"],"end":140601833,"feature_type":"variation","strand":1,"source":"dbSNP","start":140601833,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1294598847","clinical_significance":[],"end":140601834,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","start":140601834,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs770092372","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140601835,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601835},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140601836,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140601836,"source":"dbSNP","seq_region_name":"7","id":"rs775756396","clinical_significance":[]},{"seq_region_name":"7","id":"rs1264415464","clinical_significance":[],"start":140601837,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","end":140601837,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140601838,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140601838,"source":"dbSNP","seq_region_name":"7","id":"rs763102012","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799516057","seq_region_name":"7","source":"dbSNP","start":140601839,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140601839,"feature_type":"variation","strand":1},{"start":140601841,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["T","A","C"],"end":140601841,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs768813229","clinical_significance":[]},{"start":140601846,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","alleles":["A","T"],"end":140601846,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs774577195","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1184717861","end":140601851,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140601851,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"start":140601852,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","end":140601852,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs760630133","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140601853,"alleles":["G","A"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601853,"clinical_significance":[],"seq_region_name":"7","id":"rs1183910128"},{"start":140601854,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["G","T"],"end":140601854,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs779985363","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140601857,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140601857,"seq_region_name":"7","id":"rs1799517110","clinical_significance":[]},{"alleles":["G","A"],"end":140601861,"strand":1,"feature_type":"variation","start":140601861,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","id":"rs976442417","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140601863,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601863,"clinical_significance":[],"id":"rs1415880456","seq_region_name":"7"},{"start":140601864,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["A","T"],"end":140601864,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs922495647","clinical_significance":[]},{"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601870,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140601870,"clinical_significance":[],"id":"rs766405593","seq_region_name":"7"},{"start":140601872,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140601872,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1190397820","clinical_significance":[]},{"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601876,"feature_type":"variation","strand":1,"alleles":["C","A","G","T"],"end":140601876,"clinical_significance":[],"id":"rs576210233","seq_region_name":"7"},{"seq_region_name":"7","id":"rs759354546","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"stop_gained","start":140601877,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140601877},{"seq_region_name":"7","id":"rs764964047","clinical_significance":[],"end":140601880,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140601880,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"id":"rs747162996","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140601882,"source":"dbSNP","strand":1,"feature_type":"variation","end":140601882,"alleles":["A","G"]},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601884,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140601884,"clinical_significance":[],"id":"rs1799518670","seq_region_name":"7"},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601885,"feature_type":"variation","strand":1,"end":140601885,"alleles":["C","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs375700792"},{"seq_region_name":"7","id":"rs763540226","clinical_significance":[],"strand":1,"feature_type":"variation","end":140601888,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140601888,"source":"dbSNP"},{"alleles":["C","T"],"end":140601894,"strand":1,"feature_type":"variation","start":140601894,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","id":"rs751058556","seq_region_name":"7","clinical_significance":[]},{"end":140601897,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140601897,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","seq_region_name":"7","id":"rs370132781","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs543622908","consequence_type":"stop_gained","assembly_name":"GRCh38","source":"dbSNP","start":140601899,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140601899},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140601901,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601901,"clinical_significance":[],"seq_region_name":"7","id":"rs974421104"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799519729","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601902,"feature_type":"variation","strand":1,"end":140601902,"alleles":["G","C"]},{"alleles":["T","C"],"end":140601903,"strand":1,"feature_type":"variation","start":140601903,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","seq_region_name":"7","id":"rs1341755478","clinical_significance":[]},{"source":"dbSNP","start":140601908,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140601908,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs925828024","seq_region_name":"7"},{"start":140601909,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","alleles":["G","C"],"end":140601909,"strand":1,"feature_type":"variation","id":"rs746407166","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1296885608","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140601911,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140601911},{"seq_region_name":"7","id":"rs374625312","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140601912,"source":"dbSNP","strand":1,"feature_type":"variation","end":140601912,"alleles":["C","T"]},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601913,"feature_type":"variation","strand":1,"end":140601913,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1199931698"},{"source":"dbSNP","start":140601921,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","end":140601921,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs561696827"},{"clinical_significance":[],"seq_region_name":"7","id":"rs573861843","alleles":["C","T"],"end":140601923,"feature_type":"variation","strand":1,"source":"dbSNP","start":140601923,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs769689836","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140601924,"source":"dbSNP","strand":1,"feature_type":"variation","end":140601924,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1799521160","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140601926,"source":"dbSNP","strand":1,"feature_type":"variation","end":140601926,"alleles":["A","G"]},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601929,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140601929,"clinical_significance":[],"seq_region_name":"7","id":"rs774771711"},{"feature_type":"variation","strand":1,"end":140601930,"alleles":["G","A"],"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601930,"clinical_significance":[],"seq_region_name":"7","id":"rs1585733908"},{"seq_region_name":"7","id":"rs269243","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140601931,"source":"dbSNP","strand":1,"feature_type":"variation","end":140601931,"alleles":["G","A","C","T"]},{"strand":1,"feature_type":"variation","end":140601932,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140601932,"source":"dbSNP","seq_region_name":"7","id":"rs772327740","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140601935,"alleles":["C","A","G","T"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140601935,"source":"dbSNP","seq_region_name":"7","id":"rs913049832","clinical_significance":["uncertain significance"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs147680550","end":140601936,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140601936,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1799522933","clinical_significance":[],"strand":1,"feature_type":"variation","end":140601938,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140601938,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799523127","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601939,"feature_type":"variation","strand":1,"end":140601939,"alleles":["C","A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1478850291","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140601940,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601940},{"feature_type":"variation","strand":1,"end":140601941,"alleles":["G","A"],"consequence_type":"stop_gained","assembly_name":"GRCh38","source":"dbSNP","start":140601941,"clinical_significance":[],"id":"rs1799523548","seq_region_name":"7"},{"id":"rs201292153","seq_region_name":"7","clinical_significance":["uncertain significance"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140601946,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140601946},{"seq_region_name":"7","id":"rs868619288","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140601947,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140601947,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1385358939","alleles":["G","A"],"end":140601954,"feature_type":"variation","strand":1,"source":"dbSNP","start":140601954,"consequence_type":"synonymous_variant","assembly_name":"GRCh38"},{"end":140601955,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140601955,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":["uncertain significance"],"seq_region_name":"7","id":"rs775165363"},{"source":"dbSNP","start":140601957,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140601957,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799524750"},{"seq_region_name":"7","id":"rs1799524873","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140601959,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140601959,"source":"dbSNP"},{"end":140601960,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140601960,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","seq_region_name":"7","id":"rs763736116","clinical_significance":[]},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601961,"feature_type":"variation","strand":1,"end":140601961,"alleles":["C","G"],"clinical_significance":[],"id":"rs1243183033","seq_region_name":"7"},{"seq_region_name":"7","id":"rs751256899","clinical_significance":[],"strand":1,"feature_type":"variation","end":140601966,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140601966,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799525486","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601967,"feature_type":"variation","strand":1,"end":140601967,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs756734022","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140601970,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","G","T"],"end":140601970},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799525879","source":"dbSNP","start":140601974,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140601974,"feature_type":"variation","strand":1},{"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601975,"feature_type":"variation","strand":1,"end":140601975,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1439413282"},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601976,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140601976,"clinical_significance":[],"seq_region_name":"7","id":"rs200379562"},{"clinical_significance":[],"seq_region_name":"7","id":"rs913354641","feature_type":"variation","strand":1,"alleles":["CGGCCCC","CGGCCCCGGCCCC"],"end":140601982,"consequence_type":"inframe_insertion","assembly_name":"GRCh38","source":"dbSNP","start":140601976},{"alleles":["G","C"],"end":140601977,"feature_type":"variation","strand":1,"source":"dbSNP","start":140601977,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs756580492","seq_region_name":"7"},{"alleles":["C","G"],"end":140601981,"strand":1,"feature_type":"variation","start":140601981,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs1342873553","clinical_significance":[]},{"start":140601983,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["A","G"],"end":140601983,"strand":1,"feature_type":"variation","id":"rs1585734231","seq_region_name":"7","clinical_significance":["uncertain significance"]},{"clinical_significance":["uncertain significance"],"seq_region_name":"7","id":"rs1799526824","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601985,"feature_type":"variation","strand":1,"end":140601985,"alleles":["C","G","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs184946981","source":"dbSNP","start":140601989,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140601989,"alleles":["G","A","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1237862431","seq_region_name":"7","feature_type":"variation","strand":1,"end":140601992,"alleles":["C","T"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601992},{"clinical_significance":["uncertain significance"],"id":"rs375830921","seq_region_name":"7","source":"dbSNP","start":140601995,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140601995,"alleles":["C","T"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140602000,"alleles":["CCC","CCCC"],"consequence_type":"frameshift_variant","assembly_name":"GRCh38","source":"dbSNP","start":140601998,"clinical_significance":[],"seq_region_name":"7","id":"rs1316723293"},{"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140601999,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140601999,"seq_region_name":"7","id":"rs1585734298","clinical_significance":[]},{"id":"rs779244946","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140602000,"source":"dbSNP","strand":1,"feature_type":"variation","end":140602000,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs780382412","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C","T"],"end":140602001,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140602001,"source":"dbSNP"},{"start":140602002,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","alleles":["T","C"],"end":140602002,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1280248278","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1055055622","feature_type":"variation","strand":1,"end":140602004,"alleles":["C","G"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602004},{"seq_region_name":"7","id":"rs748404506","clinical_significance":[],"start":140602005,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","end":140602005,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs772239377","source":"dbSNP","start":140602007,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140602007,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1280708259","clinical_significance":[],"strand":1,"feature_type":"variation","end":140602011,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140602011,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs773171357","alleles":["T","C"],"end":140602013,"feature_type":"variation","strand":1,"source":"dbSNP","start":140602013,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs372145398","clinical_significance":["uncertain significance"],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140602015,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140602015,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585734421","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602018,"feature_type":"variation","strand":1,"end":140602018,"alleles":["T","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130687000","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602019,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140602019},{"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602020,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140602020,"clinical_significance":[],"seq_region_name":"7","id":"rs1799528995"},{"clinical_significance":["uncertain significance"],"seq_region_name":"7","id":"rs769608384","feature_type":"variation","strand":1,"end":140602022,"alleles":["G","A","T"],"consequence_type":"stop_gained","assembly_name":"GRCh38","source":"dbSNP","start":140602022},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602025,"feature_type":"variation","strand":1,"end":140602025,"alleles":["C","G"],"clinical_significance":["likely benign"],"seq_region_name":"7","id":"rs1423072997"},{"seq_region_name":"7","id":"rs375125711","clinical_significance":[],"strand":1,"feature_type":"variation","end":140602026,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140602026,"source":"dbSNP"},{"start":140602027,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140602027,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs749467796","clinical_significance":[]},{"seq_region_name":"7","id":"rs1365758419","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140602032,"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140602032,"source":"dbSNP"},{"source":"dbSNP","start":140602033,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140602033,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs773941048"},{"clinical_significance":[],"id":"rs1799530111","seq_region_name":"7","alleles":["C","A"],"end":140602038,"feature_type":"variation","strand":1,"source":"dbSNP","start":140602038,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"alleles":["C","G","T"],"end":140602042,"feature_type":"variation","strand":1,"source":"dbSNP","start":140602042,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":["uncertain significance"],"id":"rs201559363","seq_region_name":"7"},{"alleles":["CCCCC","CCCC"],"end":140602046,"feature_type":"variation","strand":1,"source":"dbSNP","start":140602042,"consequence_type":"frameshift_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130687090"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140602043,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140602043,"source":"dbSNP","seq_region_name":"7","id":"rs867110643","clinical_significance":[]},{"clinical_significance":[],"id":"rs199604652","seq_region_name":"7","feature_type":"variation","strand":1,"end":140602044,"alleles":["C","G"],"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602044},{"id":"rs749914300","seq_region_name":"7","clinical_significance":["uncertain significance"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140602045,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","G","T"],"end":140602045},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140602046,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602046,"clinical_significance":[],"seq_region_name":"7","id":"rs371567782"},{"clinical_significance":[],"id":"rs766791747","seq_region_name":"7","source":"dbSNP","start":140602047,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","end":140602047,"alleles":["G","A"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140602048,"alleles":["A","C"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602048,"clinical_significance":[],"seq_region_name":"7","id":"rs1339310652"},{"alleles":["C","T"],"end":140602049,"strand":1,"feature_type":"variation","start":140602049,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","id":"rs754435073","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1026599095","seq_region_name":"7","end":140602050,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140602050,"consequence_type":"synonymous_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["A","C","T"],"end":140602054,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140602054,"source":"dbSNP","seq_region_name":"7","id":"rs755347219","clinical_significance":[]},{"seq_region_name":"7","id":"rs1342353112","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140602057,"source":"dbSNP","strand":1,"feature_type":"variation","end":140602057,"alleles":["G","T"]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140602063,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602063,"clinical_significance":[],"seq_region_name":"7","id":"rs1218269220"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799531970","alleles":["T","C"],"end":140602066,"feature_type":"variation","strand":1,"source":"dbSNP","start":140602066,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140602074,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140602074,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs779452234"},{"end":140602078,"alleles":["CTTCT","CT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140602074,"consequence_type":"inframe_deletion","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs750413262"},{"end":140602076,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140602076,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs1214418486","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1408785308","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602079,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140602079},{"source":"dbSNP","start":140602082,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140602082,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs377279169","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs950933286","end":140602084,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140602084,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"start":140602084,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"frameshift_variant","end":140602089,"alleles":["CTCTCT","CTCTCTCTCT"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799532907","clinical_significance":[]},{"seq_region_name":"7","id":"rs1201019307","clinical_significance":[],"end":140602086,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140602086,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant"},{"clinical_significance":[],"id":"rs1245207759","seq_region_name":"7","end":140602090,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140602090,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1477861449","clinical_significance":[],"start":140602093,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140602093,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1799533420","seq_region_name":"7","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602094,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140602094},{"end":140602095,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140602095,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","seq_region_name":"7","id":"rs1799533543","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs752901983","alleles":["G","C"],"end":140602096,"feature_type":"variation","strand":1,"source":"dbSNP","start":140602096,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1177984678","clinical_significance":[],"alleles":["G","A"],"end":140602097,"strand":1,"feature_type":"variation","start":140602097,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602098,"feature_type":"variation","strand":1,"end":140602098,"alleles":["C","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1382594837"},{"clinical_significance":[],"id":"rs1418210336","seq_region_name":"7","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602099,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140602099},{"feature_type":"variation","strand":1,"end":140602100,"alleles":["T","A"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602100,"clinical_significance":[],"seq_region_name":"7","id":"rs758564518"},{"seq_region_name":"7","id":"rs1009087428","clinical_significance":[],"start":140602101,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["C","T"],"end":140602101,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140602102,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["A","C","G"],"end":140602102,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs369997641"},{"seq_region_name":"7","id":"rs1288139414","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140602104,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140602104},{"clinical_significance":["uncertain significance"],"id":"rs200519436","seq_region_name":"7","end":140602109,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140602109,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs779836361","end":140602112,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140602112,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140602115,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602115,"clinical_significance":[],"id":"rs1328829554","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140602116,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140602116,"seq_region_name":"7","id":"rs1563171487","clinical_significance":[]},{"clinical_significance":[],"id":"rs1160074671","seq_region_name":"7","end":140602119,"alleles":["CTCT","CT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140602116,"consequence_type":"frameshift_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs749242496","clinical_significance":[],"start":140602117,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140602117,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"end":140602124,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140602124,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1378883056"},{"seq_region_name":"7","id":"rs755894323","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"inframe_deletion","start":140602124,"source":"dbSNP","strand":1,"feature_type":"variation","end":140602126,"alleles":["CCT","-"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs779780810","feature_type":"variation","strand":1,"alleles":["A","-"],"end":140602128,"consequence_type":"frameshift_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602128},{"seq_region_name":"7","id":"rs749113461","clinical_significance":[],"end":140602131,"alleles":["TT","-"],"strand":1,"feature_type":"variation","start":140602130,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"frameshift_variant"},{"id":"rs1799535832","seq_region_name":"7","clinical_significance":[],"alleles":["A","G"],"end":140602135,"strand":1,"feature_type":"variation","start":140602135,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"start":140602137,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","alleles":["C","A","G"],"end":140602137,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs974368874","clinical_significance":[]},{"start":140602138,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["C","T"],"end":140602138,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs768396233","clinical_significance":[]},{"source":"dbSNP","start":140602140,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140602140,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs774134686"},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602141,"feature_type":"variation","strand":1,"end":140602141,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs761393875"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140602143,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602143,"clinical_significance":[],"id":"rs564034547","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799536697","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602147,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140602147},{"feature_type":"variation","strand":1,"alleles":["CTCCTCCTC","CTCCTC"],"end":140602155,"consequence_type":"inframe_deletion","assembly_name":"GRCh38","source":"dbSNP","start":140602147,"clinical_significance":[],"seq_region_name":"7","id":"rs754530478"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140602148,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602148,"clinical_significance":[],"seq_region_name":"7","id":"rs772983452"},{"clinical_significance":[],"seq_region_name":"7","id":"rs760072663","source":"dbSNP","start":140602149,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","end":140602149,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799537243","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602150,"feature_type":"variation","strand":1,"end":140602150,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1178336728","source":"dbSNP","start":140602153,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140602153,"alleles":["C","T"],"feature_type":"variation","strand":1},{"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602155,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140602155,"clinical_significance":[],"id":"rs1386242809","seq_region_name":"7"},{"start":140602158,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","alleles":["C","T"],"end":140602158,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs765961680","clinical_significance":[]},{"seq_region_name":"7","id":"rs368178368","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140602161,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","G"],"end":140602161},{"clinical_significance":[],"seq_region_name":"7","id":"rs760125345","end":140602162,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140602162,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602166,"feature_type":"variation","strand":1,"end":140602166,"alleles":["A","C"],"clinical_significance":[],"id":"rs765641607","seq_region_name":"7"},{"end":140602170,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140602170,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","seq_region_name":"7","id":"rs201482531","clinical_significance":[]},{"clinical_significance":["uncertain significance"],"seq_region_name":"7","id":"rs142443879","source":"dbSNP","start":140602171,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140602171,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799538586","end":140602177,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140602177,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1444315143","feature_type":"variation","strand":1,"end":140602178,"alleles":["A","G"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602178},{"clinical_significance":[],"seq_region_name":"7","id":"rs777830276","end":140602180,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140602180,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799538988","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602183,"feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140602183},{"seq_region_name":"7","id":"rs1799539163","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140602185,"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140602185,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs199780090","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602190,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140602190},{"strand":1,"feature_type":"variation","end":140602191,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140602191,"source":"dbSNP","seq_region_name":"7","id":"rs757238426","clinical_significance":[]},{"seq_region_name":"7","id":"rs1197593032","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140602193,"source":"dbSNP","strand":1,"feature_type":"variation","end":140602193,"alleles":["C","G"]},{"clinical_significance":["uncertain significance"],"id":"rs373479609","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140602196,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602196},{"seq_region_name":"7","id":"rs749152747","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140602198,"source":"dbSNP","strand":1,"feature_type":"variation","end":140602198,"alleles":["C","T"]},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140602199,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140602199,"seq_region_name":"7","id":"rs1799539940","clinical_significance":[]},{"alleles":["G","C"],"end":140602207,"strand":1,"feature_type":"variation","start":140602207,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs953956112","clinical_significance":[]},{"id":"rs768591314","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C","T"],"end":140602208,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140602208,"source":"dbSNP"},{"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602209,"feature_type":"variation","strand":1,"end":140602209,"alleles":["T","C"],"clinical_significance":[],"id":"rs556559866","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1260238963","end":140602210,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140602210,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602212,"feature_type":"variation","strand":1,"end":140602212,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1267980804"},{"clinical_significance":[],"id":"rs2130687721","seq_region_name":"7","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602213,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140602213},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140602214,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602214,"clinical_significance":[],"seq_region_name":"7","id":"rs2130687727"},{"strand":1,"feature_type":"variation","end":140602215,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140602215,"source":"dbSNP","seq_region_name":"7","id":"rs1456660549","clinical_significance":[]},{"start":140602216,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140602216,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1198231825","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585735428","source":"dbSNP","start":140602217,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140602217,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1224658846","seq_region_name":"7","feature_type":"variation","strand":1,"end":140602219,"alleles":["G","C","T"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602219},{"source":"dbSNP","start":140602223,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140602223,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799541290","seq_region_name":"7"},{"source":"dbSNP","start":140602224,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","end":140602224,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1257356072"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1444454406","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602231,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140602231},{"seq_region_name":"7","id":"rs1186091890","clinical_significance":[],"start":140602234,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["C","T"],"end":140602234,"strand":1,"feature_type":"variation"},{"start":140602235,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["C","G"],"end":140602235,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799541818","clinical_significance":[]},{"seq_region_name":"7","id":"rs1368355884","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140602239,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140602239,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1472187557","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140602241,"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140602241,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs778877690","source":"dbSNP","start":140602244,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140602244,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563171800","consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602245,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140602245},{"source":"dbSNP","start":140602247,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140602247,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs2130687826","seq_region_name":"7"},{"id":"rs1425145645","seq_region_name":"7","clinical_significance":[],"alleles":["C","A"],"end":140602251,"strand":1,"feature_type":"variation","start":140602251,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"end":140602254,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140602254,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799542632"},{"seq_region_name":"7","id":"rs1373390213","clinical_significance":[],"alleles":["T","C"],"end":140602258,"strand":1,"feature_type":"variation","start":140602258,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"source":"dbSNP","start":140602270,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140602270,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1463787438","seq_region_name":"7"},{"seq_region_name":"7","id":"rs747931112","clinical_significance":[],"start":140602275,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["G","A","T"],"end":140602275,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140602276,"consequence_type":"missense_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140602276,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1390510004"},{"source":"dbSNP","start":140602278,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140602278,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs771940915"},{"end":140602279,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140602279,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs547130877","clinical_significance":[]},{"id":"rs375948346","seq_region_name":"7","clinical_significance":["uncertain significance"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140602280,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140602280},{"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602281,"feature_type":"variation","strand":1,"end":140602281,"alleles":["G","A"],"clinical_significance":[],"id":"rs868019456","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140602283,"alleles":["G","T"],"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602283,"clinical_significance":[],"seq_region_name":"7","id":"rs770280401"},{"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140602290,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602290,"clinical_significance":[],"seq_region_name":"7","id":"rs1799544095"},{"seq_region_name":"7","id":"rs985783872","clinical_significance":[],"strand":1,"feature_type":"variation","end":140602294,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140602294,"source":"dbSNP"},{"clinical_significance":["uncertain significance"],"id":"rs1280237396","seq_region_name":"7","alleles":["G","A","T"],"end":140602301,"feature_type":"variation","strand":1,"source":"dbSNP","start":140602301,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"end":140602302,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140602302,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","seq_region_name":"7","id":"rs928017475","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563171884","end":140602303,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140602303,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"end":140602307,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140602307,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs1316119383","clinical_significance":[]},{"end":140602309,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140602309,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1385796592","seq_region_name":"7"},{"start":140602312,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","end":140602312,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs1799545076","seq_region_name":"7","clinical_significance":["uncertain significance"]},{"seq_region_name":"7","id":"rs1799545200","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140602316,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140602316},{"seq_region_name":"7","id":"rs1218292898","clinical_significance":[],"end":140602318,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140602318,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"seq_region_name":"7","id":"rs370257416","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140602323,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140602323},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140602324,"source":"dbSNP","strand":1,"feature_type":"variation","end":140602324,"alleles":["A","G"],"seq_region_name":"7","id":"rs759175577","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799545716","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140602337,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140602337},{"feature_type":"variation","strand":1,"end":140602338,"alleles":["A","G"],"consequence_type":"synonymous_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602338,"clinical_significance":[],"seq_region_name":"7","id":"rs774842835"},{"start":140602341,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","alleles":["C","T"],"end":140602341,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1256080242","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1488942180","end":140602342,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140602342,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"start":140602344,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","alleles":["G","C","T"],"end":140602344,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs200642129","clinical_significance":["uncertain significance"]},{"id":"rs763209990","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140602347,"strand":1,"feature_type":"variation","start":140602347,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant"},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140602349,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140602349,"seq_region_name":"7","id":"rs930688051","clinical_significance":[]},{"end":140602350,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140602350,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"synonymous_variant","seq_region_name":"7","id":"rs1476537936","clinical_significance":[]},{"seq_region_name":"7","id":"rs1169333710","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140602355,"source":"dbSNP","strand":1,"feature_type":"variation","end":140602355,"alleles":["C","A","T"]},{"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140602360,"source":"dbSNP","strand":1,"feature_type":"variation","end":140602360,"alleles":["G","A"],"seq_region_name":"7","id":"rs764545069","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140602363,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602363,"clinical_significance":[],"seq_region_name":"7","id":"rs1585735860"},{"end":140602366,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140602366,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant","seq_region_name":"7","id":"rs1048424441","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1188363262","end":140602367,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140602367,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs751687877","source":"dbSNP","start":140602371,"consequence_type":"synonymous_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140602371,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1170663596","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140602372,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602372},{"alleles":["T","G"],"end":140602373,"feature_type":"variation","strand":1,"source":"dbSNP","start":140602373,"consequence_type":"missense_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1484973041","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140602376,"alleles":["T","A","C"],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140602376,"source":"dbSNP","seq_region_name":"7","id":"rs757501399","clinical_significance":["uncertain significance"]},{"seq_region_name":"7","id":"rs1799548106","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"missense_variant","start":140602378,"source":"dbSNP","strand":1,"feature_type":"variation","end":140602378,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs750486337","clinical_significance":[],"end":140602381,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","start":140602381,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"missense_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs573443310","source":"dbSNP","start":140602385,"consequence_type":"missense_variant","assembly_name":"GRCh38","end":140602385,"alleles":["T","C"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140602390,"consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602390,"clinical_significance":[],"seq_region_name":"7","id":"rs1799548572"},{"id":"rs1338556967","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140602392,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"synonymous_variant","start":140602392,"source":"dbSNP"},{"clinical_significance":[],"id":"rs778789651","seq_region_name":"7","consequence_type":"missense_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602393,"feature_type":"variation","strand":1,"end":140602393,"alleles":["T","A","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799549004","end":140602394,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140602394,"consequence_type":"missense_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140602395,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"start_lost","start":140602395,"source":"dbSNP","seq_region_name":"7","id":"rs1799549127","clinical_significance":[]},{"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602398,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140602398,"clinical_significance":[],"id":"rs886709175","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799549369","clinical_significance":[],"start":140602399,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","end":140602399,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602402,"feature_type":"variation","strand":1,"end":140602402,"alleles":["G","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1563172059"},{"seq_region_name":"7","id":"rs1261698624","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140602405,"assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","start":140602405,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140602409,"alleles":["G","C"],"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602409,"clinical_significance":[],"id":"rs2130688206","seq_region_name":"7"},{"source":"dbSNP","start":140602410,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140602410,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs373669746"},{"seq_region_name":"7","id":"rs375635641","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","start":140602411,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140602411},{"alleles":["GG","G"],"end":140602416,"feature_type":"variation","strand":1,"source":"dbSNP","start":140602415,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1215944549"},{"id":"rs746585067","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","start":140602417,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140602417},{"clinical_significance":[],"seq_region_name":"7","id":"rs1354838590","source":"dbSNP","start":140602419,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140602419,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs770696125","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140602424,"assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","start":140602424,"source":"dbSNP"},{"start":140602426,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","alleles":["C","A","G"],"end":140602426,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs988691007","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs763730397","source":"dbSNP","start":140602427,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","end":140602427,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799550636","feature_type":"variation","strand":1,"alleles":["-","C"],"end":140602428,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602429},{"start":140602432,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","alleles":["A","-"],"end":140602432,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs913294218","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140602433,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602433,"clinical_significance":[],"seq_region_name":"7","id":"rs1465301288"},{"clinical_significance":[],"seq_region_name":"7","id":"rs371557509","source":"dbSNP","start":140602434,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140602434,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","start":140602435,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140602435,"seq_region_name":"7","id":"rs557441483","clinical_significance":[]},{"source":"dbSNP","start":140602436,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","end":140602436,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1172882896"},{"alleles":["A","G"],"end":140602437,"feature_type":"variation","strand":1,"source":"dbSNP","start":140602437,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130688303"},{"seq_region_name":"7","id":"rs1267433195","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140602440,"assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","start":140602440,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs995919943","feature_type":"variation","strand":1,"end":140602445,"alleles":["T","C"],"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602445},{"clinical_significance":[],"seq_region_name":"7","id":"rs1032791308","alleles":["C","T"],"end":140602450,"feature_type":"variation","strand":1,"source":"dbSNP","start":140602450,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140602450,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","alleles":["CC","C"],"end":140602451,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1447866879","seq_region_name":"7"},{"end":140602452,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140602452,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","seq_region_name":"7","id":"rs189834917","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140602460,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602460,"clinical_significance":[],"id":"rs867395321","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799552244","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","start":140602462,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140602462},{"seq_region_name":"7","id":"rs2130688355","clinical_significance":[],"end":140602463,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140602463,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant"},{"seq_region_name":"7","id":"rs1799552342","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","start":140602464,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140602464},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799552441","consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602467,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140602467},{"seq_region_name":"7","id":"rs1585736195","clinical_significance":[],"start":140602472,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","alleles":["G","A","C"],"end":140602472,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799552687","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140602481,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602481},{"clinical_significance":[],"id":"rs146748385","seq_region_name":"7","feature_type":"variation","strand":1,"end":140602482,"alleles":["G","A"],"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602482},{"clinical_significance":[],"seq_region_name":"7","id":"rs1191390365","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140602504,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602504},{"start":140602505,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","alleles":["G","A","C"],"end":140602505,"strand":1,"feature_type":"variation","id":"rs1200248155","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799553127","clinical_significance":[],"alleles":["G","C"],"end":140602507,"strand":1,"feature_type":"variation","start":140602507,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant"},{"feature_type":"variation","strand":1,"end":140602510,"alleles":["T","G"],"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602510,"clinical_significance":[],"seq_region_name":"7","id":"rs1585736241"},{"source":"dbSNP","start":140602512,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","end":140602512,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1020591762","seq_region_name":"7"},{"end":140602513,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140602513,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs762425095"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799553543","source":"dbSNP","start":140602520,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140602520,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1799553624","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140602525,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602525},{"strand":1,"feature_type":"variation","alleles":["CCTTCC","CCTTCCTTCC"],"end":140602533,"assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","start":140602528,"source":"dbSNP","seq_region_name":"7","id":"rs1799553731","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","start":140602530,"source":"dbSNP","strand":1,"feature_type":"variation","end":140602530,"alleles":["T","G"],"seq_region_name":"7","id":"rs1180261959","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799553944","clinical_significance":[],"strand":1,"feature_type":"variation","end":140602533,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","start":140602533,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799554049","clinical_significance":[],"end":140602535,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140602535,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant"},{"alleles":["C","T"],"end":140602536,"feature_type":"variation","strand":1,"source":"dbSNP","start":140602536,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1339581302"},{"start":140602541,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_region_variant","alleles":["C","T"],"end":140602541,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs114649272","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1049767303","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140602542,"consequence_type":"splice_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602542},{"strand":1,"feature_type":"variation","end":140602543,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"splice_acceptor_variant","start":140602543,"source":"dbSNP","seq_region_name":"7","id":"rs1799554470","clinical_significance":[]},{"end":140602544,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140602544,"consequence_type":"splice_acceptor_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799554542","seq_region_name":"7"},{"consequence_type":"splice_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602545,"feature_type":"variation","strand":1,"end":140602545,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799554622"},{"seq_region_name":"7","id":"rs888062255","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"splice_region_variant","start":140602546,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140602546},{"alleles":["C","A"],"end":140602548,"feature_type":"variation","strand":1,"source":"dbSNP","start":140602548,"consequence_type":"splice_region_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1310567277"},{"source":"dbSNP","start":140602563,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["CC","CCC"],"end":140602564,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799554943"},{"feature_type":"variation","strand":1,"end":140602567,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602567,"clinical_significance":[],"id":"rs1563172224","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1395370754","clinical_significance":[],"strand":1,"feature_type":"variation","end":140602581,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140602581,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602584,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140602584,"clinical_significance":[],"seq_region_name":"7","id":"rs2130688535"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140602586,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140602586,"source":"dbSNP","id":"rs1373847232","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130688551","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602590,"feature_type":"variation","strand":1,"end":140602590,"alleles":["G","A"]},{"strand":1,"feature_type":"variation","end":140602595,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140602595,"source":"dbSNP","seq_region_name":"7","id":"rs927124698","clinical_significance":[]},{"source":"dbSNP","start":140602597,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140602597,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130688561"},{"seq_region_name":"7","id":"rs937207701","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140602599,"source":"dbSNP","strand":1,"feature_type":"variation","end":140602599,"alleles":["A","G"]},{"clinical_significance":[],"id":"rs1799555573","seq_region_name":"7","alleles":["G","A"],"end":140602600,"feature_type":"variation","strand":1,"source":"dbSNP","start":140602600,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140602602,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602602,"clinical_significance":[],"id":"rs1428099188","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1370139122","clinical_significance":[],"strand":1,"feature_type":"variation","end":140602608,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140602608,"source":"dbSNP"},{"end":140602611,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140602611,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1452269840"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1164315286","source":"dbSNP","start":140602620,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140602620,"feature_type":"variation","strand":1},{"alleles":["T","C"],"end":140602622,"feature_type":"variation","strand":1,"source":"dbSNP","start":140602622,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585736438"},{"id":"rs990849451","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140602624,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140602624,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1426559466","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602625,"feature_type":"variation","strand":1,"end":140602625,"alleles":["A","C"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602626,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140602626,"clinical_significance":[],"id":"rs1799556285","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1366779700","clinical_significance":[],"alleles":["T","C"],"end":140602629,"strand":1,"feature_type":"variation","start":140602629,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140602631,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140602631,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1288307357","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","A","T"],"end":140602634,"strand":1,"feature_type":"variation","start":140602634,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585736472","clinical_significance":[]},{"start":140602641,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140602641,"strand":1,"feature_type":"variation","id":"rs1420169757","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140602642,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140602642,"source":"dbSNP","seq_region_name":"7","id":"rs1253137218","clinical_significance":[]},{"alleles":["A","G"],"end":140602645,"strand":1,"feature_type":"variation","start":140602645,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1391576925","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799557010","clinical_significance":[],"end":140602648,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140602648,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1799557120","clinical_significance":[],"end":140602649,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140602649,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140602650,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140602650,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799557216","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585736520","end":140602653,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140602653,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs573928358","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602655,"feature_type":"variation","strand":1,"end":140602655,"alleles":["T","C"]},{"source":"dbSNP","start":140602661,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140602661,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1301486830"},{"feature_type":"variation","strand":1,"end":140602663,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602663,"clinical_significance":[],"seq_region_name":"7","id":"rs1563172295"},{"clinical_significance":[],"id":"rs930612625","seq_region_name":"7","end":140602664,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140602664,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140602666,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140602666,"source":"dbSNP","seq_region_name":"7","id":"rs147942331","clinical_significance":[]},{"start":140602668,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140602668,"alleles":["T","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs112964010","clinical_significance":[]},{"id":"rs111737412","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140602669,"source":"dbSNP","strand":1,"feature_type":"variation","end":140602669,"alleles":["A","T"]},{"source":"dbSNP","start":140602669,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AAAAAAAAAAA","AAAAAAAAAA","AAAAAAAAAAAA"],"end":140602679,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs201951571","seq_region_name":"7"},{"seq_region_name":"7","id":"rs889447750","clinical_significance":[],"start":140602670,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C","T"],"end":140602670,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1799558400","clinical_significance":[],"end":140602675,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140602675,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799558498","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602676,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140602676},{"end":140602680,"alleles":["AT","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140602679,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs563908273"},{"source":"dbSNP","start":140602680,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140602680,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1244027757"},{"seq_region_name":"7","id":"rs1317404387","clinical_significance":[],"start":140602682,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140602682,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs944977271","clinical_significance":[],"strand":1,"feature_type":"variation","end":140602683,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140602683,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799559013","clinical_significance":[],"strand":1,"feature_type":"variation","end":140602684,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140602684,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140602686,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602686,"clinical_significance":[],"seq_region_name":"7","id":"rs1311189981"},{"start":140602694,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140602694,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1040684122","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140602698,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140602698,"id":"rs1585736676","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1314994966","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140602699,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602699},{"alleles":["C","T"],"end":140602706,"feature_type":"variation","strand":1,"source":"dbSNP","start":140602706,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1407707832","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799559611","clinical_significance":[],"alleles":["T","C"],"end":140602707,"strand":1,"feature_type":"variation","start":140602707,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140602708,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140602708,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799559714","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140602710,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602710,"clinical_significance":[],"seq_region_name":"7","id":"rs2130688766"},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140602712,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140602712,"source":"dbSNP","seq_region_name":"7","id":"rs900659926","clinical_significance":[]},{"clinical_significance":[],"id":"rs1350111373","seq_region_name":"7","end":140602715,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140602715,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs996371333","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602724,"feature_type":"variation","strand":1,"end":140602724,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1304055681","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602725,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140602725},{"id":"rs1799560391","seq_region_name":"7","clinical_significance":[],"start":140602726,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140602726,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1215010679","source":"dbSNP","start":140602738,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140602738,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140602739,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602739,"clinical_significance":[],"seq_region_name":"7","id":"rs2130688805"},{"seq_region_name":"7","id":"rs578126088","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140602741,"source":"dbSNP","strand":1,"feature_type":"variation","end":140602741,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1489155398","clinical_significance":[],"start":140602742,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140602742,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1211327469","clinical_significance":[],"start":140602743,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140602743,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs892898938","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140602747,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140602747},{"seq_region_name":"7","id":"rs1454781096","clinical_significance":[],"strand":1,"feature_type":"variation","end":140602749,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140602749,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1439991320","clinical_significance":[],"start":140602752,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140602752,"alleles":["C","A","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs140591654","end":140602753,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140602753,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140602756,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140602756,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1157400532","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140602758,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602758,"clinical_significance":[],"seq_region_name":"7","id":"rs988575045"},{"source":"dbSNP","start":140602761,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140602761,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1270031895"},{"source":"dbSNP","start":140602765,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140602765,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs563568294","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1417804969","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["CC","C"],"end":140602776,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602775},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799562676","feature_type":"variation","strand":1,"end":140602776,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602776},{"strand":1,"feature_type":"variation","end":140602777,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140602777,"source":"dbSNP","seq_region_name":"7","id":"rs1799562831","clinical_significance":[]},{"clinical_significance":[],"id":"rs1159062062","seq_region_name":"7","source":"dbSNP","start":140602778,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140602778,"alleles":["G","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799563163","alleles":["C","A"],"end":140602779,"feature_type":"variation","strand":1,"source":"dbSNP","start":140602779,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140602780,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602780,"clinical_significance":[],"seq_region_name":"7","id":"rs1351016624"},{"clinical_significance":[],"id":"rs762918994","seq_region_name":"7","feature_type":"variation","strand":1,"end":140602785,"alleles":["CTGGGC","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602780},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140602782,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140602782,"seq_region_name":"7","id":"rs1208678049","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1019950725","feature_type":"variation","strand":1,"end":140602788,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602788},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799563956","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602790,"feature_type":"variation","strand":1,"end":140602790,"alleles":["T","A","C"]},{"seq_region_name":"7","id":"rs1799564149","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140602797,"source":"dbSNP","strand":1,"feature_type":"variation","end":140602797,"alleles":["A","G"]},{"start":140602801,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140602801,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs6464879","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140602802,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140602802,"source":"dbSNP","seq_region_name":"7","id":"rs549459485","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1226496627","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140602806,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602806},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799564861","source":"dbSNP","start":140602808,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140602808,"feature_type":"variation","strand":1},{"start":140602810,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140602810,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs10264061","clinical_significance":[]},{"source":"dbSNP","start":140602811,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AAAAA","AAAAAA"],"end":140602815,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1283645505","seq_region_name":"7"},{"alleles":["A","C"],"end":140602814,"feature_type":"variation","strand":1,"source":"dbSNP","start":140602814,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1329509196"},{"feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140602815,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602815,"clinical_significance":[],"id":"rs372014518","seq_region_name":"7"},{"id":"rs867995370","seq_region_name":"7","clinical_significance":[],"alleles":["T","A"],"end":140602816,"strand":1,"feature_type":"variation","start":140602816,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1322986952","seq_region_name":"7","clinical_significance":[],"start":140602816,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TTTTTTTT","TTTTTTT","TTTTTTTTT"],"end":140602823,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs542317068","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602818,"feature_type":"variation","strand":1,"end":140602818,"alleles":["T","A"]},{"clinical_significance":[],"id":"rs192171690","seq_region_name":"7","source":"dbSNP","start":140602823,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140602823,"alleles":["T","A"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602824,"feature_type":"variation","strand":1,"end":140602824,"alleles":["A","C"],"clinical_significance":[],"id":"rs1799566393","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140602829,"source":"dbSNP","strand":1,"feature_type":"variation","end":140602829,"alleles":["C","T"],"seq_region_name":"7","id":"rs1799566557","clinical_significance":[]},{"seq_region_name":"7","id":"rs940966910","clinical_significance":[],"alleles":["T","G"],"end":140602830,"strand":1,"feature_type":"variation","start":140602830,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1799566702","clinical_significance":[],"alleles":["C","T"],"end":140602831,"strand":1,"feature_type":"variation","start":140602831,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140602833,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140602833,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1370948485"},{"end":140602835,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140602835,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs920643548"},{"clinical_significance":[],"seq_region_name":"7","id":"rs930750183","alleles":["G","A"],"end":140602837,"feature_type":"variation","strand":1,"source":"dbSNP","start":140602837,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140602842,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140602842,"alleles":["T","G"],"strand":1,"feature_type":"variation","id":"rs1799567374","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140602849,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140602849,"source":"dbSNP","seq_region_name":"7","id":"rs1799567518","clinical_significance":[]},{"alleles":["-","TT"],"end":140602854,"strand":1,"feature_type":"variation","start":140602855,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130689081","clinical_significance":[]},{"alleles":["C","T"],"end":140602855,"feature_type":"variation","strand":1,"source":"dbSNP","start":140602855,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799567655"},{"strand":1,"feature_type":"variation","end":140602856,"alleles":["-","TTTCATCATT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140602857,"source":"dbSNP","seq_region_name":"7","id":"rs2130689097","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs751800913","source":"dbSNP","start":140602857,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140602857,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140602860,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140602860,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs902017275"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602862,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140602862,"clinical_significance":[],"seq_region_name":"7","id":"rs983982988"},{"end":140602868,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140602868,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1585737091","seq_region_name":"7"},{"end":140602869,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140602869,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799568330"},{"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140602870,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140602870,"source":"dbSNP","id":"rs1799568428","seq_region_name":"7","clinical_significance":[]},{"start":140602871,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140602871,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1447145981","clinical_significance":[]},{"source":"dbSNP","start":140602880,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140602880,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1249335380","seq_region_name":"7"},{"alleles":["G","A","C"],"end":140602881,"feature_type":"variation","strand":1,"source":"dbSNP","start":140602881,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs907863291"},{"source":"dbSNP","start":140602883,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140602883,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs944733913"},{"clinical_significance":[],"id":"rs1201904487","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140602888,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602888},{"seq_region_name":"7","id":"rs184910944","clinical_significance":[],"start":140602895,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140602895,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs565459316","end":140602897,"alleles":["T","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140602897,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140602900,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140602900,"strand":1,"feature_type":"variation","id":"rs1230915552","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799569391","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140602901,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602901},{"alleles":["T","G"],"end":140602903,"feature_type":"variation","strand":1,"source":"dbSNP","start":140602903,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs755007367"},{"source":"dbSNP","start":140602906,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140602906,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1271995781","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585737184","source":"dbSNP","start":140602907,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140602907,"alleles":["T","G"],"feature_type":"variation","strand":1},{"id":"rs1457890770","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140602910,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AAA","AAAA"],"end":140602912},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140602913,"source":"dbSNP","strand":1,"feature_type":"variation","end":140602913,"alleles":["T","G"],"seq_region_name":"7","id":"rs10273827","clinical_significance":[]},{"end":140602914,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140602914,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799570030"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602915,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140602915,"clinical_significance":[],"id":"rs1234925748","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140602919,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140602919,"source":"dbSNP","seq_region_name":"7","id":"rs1295457027","clinical_significance":[]},{"source":"dbSNP","start":140602926,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140602926,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799570350","seq_region_name":"7"},{"id":"rs1799570456","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140602927,"source":"dbSNP","strand":1,"feature_type":"variation","end":140602927,"alleles":["C","T"]},{"id":"rs1054635013","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140602928,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140602928,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140602935,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140602935,"source":"dbSNP","seq_region_name":"7","id":"rs1799570656","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602937,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140602937,"clinical_significance":[],"id":"rs892838133","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1407419404","feature_type":"variation","strand":1,"alleles":["TTGTTT","TT"],"end":140602948,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140602943},{"start":140602944,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140602944,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1339122741","clinical_significance":[]},{"end":140602945,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140602945,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1799571038","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1009985445","end":140602953,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140602953,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140602953,"source":"dbSNP","strand":1,"feature_type":"variation","end":140602954,"alleles":["CC","C"],"id":"rs1799571257","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","C","G"],"end":140602955,"strand":1,"feature_type":"variation","start":140602955,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs781250089","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1475517718","source":"dbSNP","start":140602962,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140602962,"alleles":["C","T"],"feature_type":"variation","strand":1},{"id":"rs189623688","seq_region_name":"7","clinical_significance":[],"end":140602987,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140602987,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799571688","source":"dbSNP","start":140602988,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140602988,"alleles":["G","C"],"feature_type":"variation","strand":1},{"start":140602991,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140602991,"strand":1,"feature_type":"variation","id":"rs1799571785","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140602992,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140602992,"source":"dbSNP","seq_region_name":"7","id":"rs1391511108","clinical_significance":[]},{"seq_region_name":"7","id":"rs569576717","clinical_significance":[],"end":140602998,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140602998,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1799572082","seq_region_name":"7","clinical_significance":[],"end":140603002,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140603002,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs180832662","clinical_significance":[],"start":140603007,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C","G"],"end":140603007,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603008,"feature_type":"variation","strand":1,"end":140603008,"alleles":["G","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799572291"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603011,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140603011,"clinical_significance":[],"id":"rs1799572386","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799572481","alleles":["T","C"],"end":140603012,"feature_type":"variation","strand":1,"source":"dbSNP","start":140603012,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","T"],"end":140603018,"strand":1,"feature_type":"variation","start":140603018,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799572584","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140603020,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603020,"clinical_significance":[],"seq_region_name":"7","id":"rs1799572664"},{"clinical_significance":[],"id":"rs1448802396","seq_region_name":"7","alleles":["A","T"],"end":140603021,"feature_type":"variation","strand":1,"source":"dbSNP","start":140603021,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1243605888","seq_region_name":"7","feature_type":"variation","strand":1,"end":140603023,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603023},{"end":140603024,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140603024,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799572987"},{"id":"rs1799573092","seq_region_name":"7","clinical_significance":[],"start":140603026,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140603026,"alleles":["T","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1189526530","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603032,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140603032},{"end":140603034,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140603034,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1177040457"},{"id":"rs1415143633","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603037,"source":"dbSNP","strand":1,"feature_type":"variation","end":140603037,"alleles":["C","A"]},{"seq_region_name":"7","id":"rs1799573508","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["TTT","TT"],"end":140603042,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603040,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603041,"source":"dbSNP","strand":1,"feature_type":"variation","end":140603041,"alleles":["T","G"],"id":"rs57570112","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140603044,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603044,"clinical_significance":[],"seq_region_name":"7","id":"rs1002516268"},{"alleles":["G","A"],"end":140603045,"strand":1,"feature_type":"variation","start":140603045,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1196644559","clinical_significance":[]},{"id":"rs1344538432","seq_region_name":"7","clinical_significance":[],"alleles":["C","G"],"end":140603049,"strand":1,"feature_type":"variation","start":140603049,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140603050,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140603050,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs770925993"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603051,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140603051,"clinical_significance":[],"seq_region_name":"7","id":"rs958624906"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140603053,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603053,"clinical_significance":[],"id":"rs1799574280","seq_region_name":"7"},{"id":"rs995263330","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603055,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140603055},{"seq_region_name":"7","id":"rs1026819718","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603056,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140603056},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603059,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","G"],"end":140603059,"seq_region_name":"7","id":"rs1417275351","clinical_significance":[]},{"start":140603060,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140603060,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs1799574748","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","G"],"end":140603062,"strand":1,"feature_type":"variation","start":140603062,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1340302727","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1329912678","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603063,"feature_type":"variation","strand":1,"end":140603063,"alleles":["T","C"]},{"end":140603066,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140603066,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1466302271"},{"clinical_significance":[],"id":"rs1010111880","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603069,"feature_type":"variation","strand":1,"end":140603069,"alleles":["G","A"]},{"start":140603071,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140603071,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs969920447","clinical_significance":[]},{"start":140603078,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140603078,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585737472","clinical_significance":[]},{"id":"rs778544937","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140603085,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603085,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603088,"source":"dbSNP","strand":1,"feature_type":"variation","end":140603088,"alleles":["G","T"],"seq_region_name":"7","id":"rs1799575551","clinical_significance":[]},{"end":140603089,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140603089,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799575659"},{"seq_region_name":"7","id":"rs1799575788","clinical_significance":[],"alleles":["G","A"],"end":140603093,"strand":1,"feature_type":"variation","start":140603093,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140603094,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603094,"clinical_significance":[],"id":"rs951326642","seq_region_name":"7"},{"end":140603095,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140603095,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1428620105","seq_region_name":"7","clinical_significance":[]},{"start":140603099,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140603099,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585737510","clinical_significance":[]},{"start":140603100,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140603100,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs573939004","clinical_significance":[]},{"start":140603102,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140603102,"strand":1,"feature_type":"variation","id":"rs1183577534","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","A"],"end":140603104,"feature_type":"variation","strand":1,"source":"dbSNP","start":140603104,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799576392","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140603108,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603108,"source":"dbSNP","seq_region_name":"7","id":"rs1471751551","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs186075794","feature_type":"variation","strand":1,"end":140603111,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603111},{"clinical_significance":[],"seq_region_name":"7","id":"rs966011948","source":"dbSNP","start":140603112,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140603112,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603116,"feature_type":"variation","strand":1,"end":140603116,"alleles":["G","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585737578"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799576916","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603117,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140603117},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603119,"feature_type":"variation","strand":1,"end":140603119,"alleles":["C","T"],"clinical_significance":[],"id":"rs971193969","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs138336278","source":"dbSNP","start":140603121,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140603121,"alleles":["A","G"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603123,"source":"dbSNP","strand":1,"feature_type":"variation","end":140603123,"alleles":["A","G"],"seq_region_name":"7","id":"rs77635335","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140603126,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603126,"clinical_significance":[],"id":"rs1799577346","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1441186955","source":"dbSNP","start":140603132,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140603132,"alleles":["G","A","C"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140603137,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603137,"source":"dbSNP","seq_region_name":"7","id":"rs1799577585","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs148816589","end":140603138,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140603138,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs575802998","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603139,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140603139},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585737657","source":"dbSNP","start":140603140,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140603140,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799577956","source":"dbSNP","start":140603143,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140603143,"feature_type":"variation","strand":1},{"start":140603144,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140603144,"alleles":["G","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799578043","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140603149,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603149,"source":"dbSNP","seq_region_name":"7","id":"rs1799578151","clinical_significance":[]},{"clinical_significance":[],"id":"rs775171082","seq_region_name":"7","source":"dbSNP","start":140603150,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140603150,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799578376","source":"dbSNP","start":140603154,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140603154,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140603166,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140603166,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799578478","seq_region_name":"7"},{"start":140603180,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140603180,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130689790","clinical_significance":[]},{"seq_region_name":"7","id":"rs1412875599","clinical_significance":[],"start":140603182,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140603182,"alleles":["A","-"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799578694","end":140603183,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140603183,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1799578782","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603185,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140603185},{"seq_region_name":"7","id":"rs1799578883","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140603189,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603189,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1055154639","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140603190,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603190},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140603191,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603191,"source":"dbSNP","seq_region_name":"7","id":"rs1799579096","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140603192,"alleles":["A","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603192,"clinical_significance":[],"seq_region_name":"7","id":"rs1292084703"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799579311","alleles":["AGGAG","AG"],"end":140603196,"feature_type":"variation","strand":1,"source":"dbSNP","start":140603192,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140603193,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140603193,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799579409"},{"id":"rs1318043312","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140603199,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603199,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603200,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140603200,"id":"rs1349010662","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603201,"feature_type":"variation","strand":1,"end":140603201,"alleles":["G","T"],"clinical_significance":[],"id":"rs1305857809","seq_region_name":"7"},{"id":"rs1408813868","seq_region_name":"7","clinical_significance":[],"end":140603204,"alleles":["G","C","T"],"strand":1,"feature_type":"variation","start":140603204,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603207,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140603207,"seq_region_name":"7","id":"rs1585737730","clinical_significance":[]},{"start":140603208,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["CCC","CC"],"end":140603210,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1166240294","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140603210,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603210,"source":"dbSNP","id":"rs914736689","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603211,"source":"dbSNP","strand":1,"feature_type":"variation","end":140603211,"alleles":["G","A","C","T"],"seq_region_name":"7","id":"rs1158937243","clinical_significance":[]},{"source":"dbSNP","start":140603211,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["GGG","GG"],"end":140603213,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs34394490"},{"seq_region_name":"7","id":"rs1585737790","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603212,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140603212},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603215,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140603215,"id":"rs1270420222","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603219,"source":"dbSNP","strand":1,"feature_type":"variation","end":140603219,"alleles":["G","C"],"id":"rs1306619656","seq_region_name":"7","clinical_significance":[]},{"end":140603229,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140603229,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1799581024","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603233,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140603233,"seq_region_name":"7","id":"rs1799581139","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1204264603","end":140603237,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140603237,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140603240,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603240,"clinical_significance":[],"id":"rs1409472919","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799581489","alleles":["C","T"],"end":140603242,"feature_type":"variation","strand":1,"source":"dbSNP","start":140603242,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799581611","end":140603244,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140603244,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs946233386","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603248,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140603248},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603249,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","-"],"end":140603249,"seq_region_name":"7","id":"rs1258661114","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs564871913","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140603252,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603252},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140603254,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603254,"clinical_significance":[],"seq_region_name":"7","id":"rs1186461078"},{"seq_region_name":"7","id":"rs1563172691","clinical_significance":[],"alleles":["CCAGCC","CC"],"end":140603259,"strand":1,"feature_type":"variation","start":140603254,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1585737889","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603258,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140603258},{"seq_region_name":"7","id":"rs1799582395","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140603260,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603260,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1248547121","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603262,"feature_type":"variation","strand":1,"end":140603262,"alleles":["G","C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1041446757","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603267,"feature_type":"variation","strand":1,"end":140603267,"alleles":["C","G"]},{"strand":1,"feature_type":"variation","alleles":["AGAGAGAGA","AGAGAGAGAGA"],"end":140603276,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603268,"source":"dbSNP","seq_region_name":"7","id":"rs1799582765","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799582890","seq_region_name":"7","feature_type":"variation","strand":1,"end":140603270,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603270},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140603277,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603277,"source":"dbSNP","seq_region_name":"7","id":"rs557425697","clinical_significance":[]},{"start":140603277,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140603280,"alleles":["CTCT","CT"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1219385233","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799583265","clinical_significance":[],"start":140603279,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140603279,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140603282,"alleles":["TGT","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603280,"source":"dbSNP","id":"rs1257479757","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs773523088","clinical_significance":[],"end":140603307,"alleles":["AAAAATAAAAATAAAAATAAAA","AAAAATAAAAATAAAA","AAAAATAAAAATAAAAATAAAAATAAAA"],"strand":1,"feature_type":"variation","start":140603286,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1002462218","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603307,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140603307},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799584013","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140603308,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603308},{"end":140603320,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140603320,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799584172"},{"end":140603320,"alleles":["C","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140603320,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799584342"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799584511","alleles":["C","T"],"end":140603322,"feature_type":"variation","strand":1,"source":"dbSNP","start":140603322,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["G","A"],"end":140603323,"feature_type":"variation","strand":1,"source":"dbSNP","start":140603323,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs575590302"},{"seq_region_name":"7","id":"rs923551588","clinical_significance":[],"strand":1,"feature_type":"variation","end":140603332,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603332,"source":"dbSNP"},{"id":"rs1227434576","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603334,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140603334},{"clinical_significance":[],"seq_region_name":"7","id":"rs80131743","source":"dbSNP","start":140603337,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140603337,"alleles":["C","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1294787833","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603338,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140603338},{"alleles":["T","A"],"end":140603339,"strand":1,"feature_type":"variation","start":140603339,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1799585700","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1433594437","clinical_significance":[],"strand":1,"feature_type":"variation","end":140603341,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603341,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1348792164","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603342,"source":"dbSNP","strand":1,"feature_type":"variation","end":140603342,"alleles":["G","T"]},{"strand":1,"feature_type":"variation","end":140603346,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603346,"source":"dbSNP","seq_region_name":"7","id":"rs527982290","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603352,"feature_type":"variation","strand":1,"end":140603352,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1027345594"},{"end":140603354,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140603354,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799586617","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603359,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140603359,"clinical_significance":[],"seq_region_name":"7","id":"rs1409540925"},{"source":"dbSNP","start":140603360,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140603360,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799586958"},{"source":"dbSNP","start":140603362,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140603362,"alleles":["T","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1176452287"},{"seq_region_name":"7","id":"rs1799587262","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603363,"source":"dbSNP","strand":1,"feature_type":"variation","end":140603363,"alleles":["A","G"]},{"clinical_significance":[],"id":"rs1799587439","seq_region_name":"7","alleles":["G","C"],"end":140603371,"feature_type":"variation","strand":1,"source":"dbSNP","start":140603371,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1799587594","clinical_significance":[],"start":140603373,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140603373,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"id":"rs1585738038","seq_region_name":"7","clinical_significance":[],"alleles":["T","G"],"end":140603375,"strand":1,"feature_type":"variation","start":140603375,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["T","A","C"],"end":140603376,"feature_type":"variation","strand":1,"source":"dbSNP","start":140603376,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1480892096"},{"end":140603377,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140603377,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799588151","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603378,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140603378,"clinical_significance":[],"seq_region_name":"7","id":"rs269244"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603380,"feature_type":"variation","strand":1,"end":140603380,"alleles":["T","A"],"clinical_significance":[],"id":"rs1004473329","seq_region_name":"7"},{"id":"rs1799588707","seq_region_name":"7","clinical_significance":[],"end":140603384,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140603384,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs540441671","seq_region_name":"7","source":"dbSNP","start":140603386,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140603386,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603387,"feature_type":"variation","strand":1,"end":140603387,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs559478762"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1242750662","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603391,"feature_type":"variation","strand":1,"end":140603391,"alleles":["T","C"]},{"end":140603393,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140603393,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799589396"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799589507","end":140603399,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140603399,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140603404,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140603404,"alleles":["A","G"],"strand":1,"feature_type":"variation","id":"rs1211167096","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1463903545","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603409,"feature_type":"variation","strand":1,"end":140603409,"alleles":["A","G","T"]},{"seq_region_name":"7","id":"rs189507787","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140603411,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603411,"source":"dbSNP"},{"source":"dbSNP","start":140603413,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140603413,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs976041201"},{"clinical_significance":[],"id":"rs1312170587","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140603423,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603423},{"clinical_significance":[],"seq_region_name":"7","id":"rs1267918824","end":140603427,"alleles":["TTT","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140603425,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1204646656","alleles":["C","T"],"end":140603434,"feature_type":"variation","strand":1,"source":"dbSNP","start":140603434,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140603435,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140603435,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585738169"},{"seq_region_name":"7","id":"rs1585738180","clinical_significance":[],"start":140603436,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140603436,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1799590621","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603437,"feature_type":"variation","strand":1,"end":140603437,"alleles":["C","G"]},{"start":140603441,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140603441,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs73165440","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130690333","feature_type":"variation","strand":1,"end":140603443,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603443},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799590866","end":140603445,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140603445,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1303028146","seq_region_name":"7","clinical_significance":[],"start":140603447,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140603447,"strand":1,"feature_type":"variation"},{"end":140603448,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140603448,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799591078","clinical_significance":[]},{"seq_region_name":"7","id":"rs1217109923","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603448,"source":"dbSNP","strand":1,"feature_type":"variation","end":140603450,"alleles":["AAA","A"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603451,"feature_type":"variation","strand":1,"end":140603451,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130690359"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1366335854","source":"dbSNP","start":140603460,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140603460,"alleles":["T","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs953392588","source":"dbSNP","start":140603463,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140603463,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603464,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140603464,"clinical_significance":[],"id":"rs1799591557","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1267968557","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603467,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140603467},{"seq_region_name":"7","id":"rs1799591799","clinical_significance":[],"alleles":["C","G"],"end":140603469,"strand":1,"feature_type":"variation","start":140603469,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140603473,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603473,"source":"dbSNP","seq_region_name":"7","id":"rs1799591901","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140603476,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603476,"clinical_significance":[],"seq_region_name":"7","id":"rs990401427"},{"start":140603478,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140603478,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1386286895","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1319664372","source":"dbSNP","start":140603479,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140603479,"alleles":["A","G"],"feature_type":"variation","strand":1},{"end":140603480,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140603480,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1466412926","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799592472","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603480,"feature_type":"variation","strand":1,"end":140603485,"alleles":["TGATTG","TG"]},{"end":140603481,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140603481,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1009889097"},{"start":140603486,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140603486,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799592686","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1174274876","alleles":["A","G"],"end":140603487,"feature_type":"variation","strand":1,"source":"dbSNP","start":140603487,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs181119342","clinical_significance":[],"end":140603488,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140603488,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603498,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140603498,"seq_region_name":"7","id":"rs1414101152","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1420346256","source":"dbSNP","start":140603499,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140603499,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799593223","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603502,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140603502},{"seq_region_name":"7","id":"rs1799593301","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603503,"source":"dbSNP","strand":1,"feature_type":"variation","end":140603503,"alleles":["C","A"]},{"end":140603506,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140603506,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1041600932","clinical_significance":[]},{"alleles":["C","T"],"end":140603507,"strand":1,"feature_type":"variation","start":140603507,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1448208413","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799593611","seq_region_name":"7","feature_type":"variation","strand":1,"end":140603510,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603510},{"clinical_significance":[],"seq_region_name":"7","id":"rs1247887840","end":140603513,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140603513,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603518,"source":"dbSNP","strand":1,"feature_type":"variation","end":140603518,"alleles":["G","A","T"],"seq_region_name":"7","id":"rs914830197","clinical_significance":[]},{"id":"rs1184736250","seq_region_name":"7","clinical_significance":[],"end":140603520,"alleles":["GC","-"],"strand":1,"feature_type":"variation","start":140603519,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140603520,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603520,"clinical_significance":[],"seq_region_name":"7","id":"rs907150574"},{"seq_region_name":"7","id":"rs1799594115","clinical_significance":[],"start":140603528,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140603528,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603530,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140603530,"seq_region_name":"7","id":"rs1219468738","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1207643436","source":"dbSNP","start":140603531,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140603531,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603541,"source":"dbSNP","strand":1,"feature_type":"variation","end":140603541,"alleles":["A","G"],"id":"rs1799594405","seq_region_name":"7","clinical_significance":[]},{"alleles":["GCCTTGCCACCAGGGCAGGGATTATTCTGTTATTTTGGCCT","GCCTTGCCACCAGGGCAGGGATTATTCTGTTATTTTGGCCTTGCCACCAGGGCAGGGATTATTCTGTTATTTTGGCCT"],"end":140603585,"strand":1,"feature_type":"variation","start":140603545,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799594510","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799594626","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140603555,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603555,"source":"dbSNP"},{"start":140603556,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140603556,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1281442577","clinical_significance":[]},{"seq_region_name":"7","id":"rs946210996","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603557,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140603557},{"end":140603558,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140603558,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799594877"},{"strand":1,"feature_type":"variation","end":140603564,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603564,"source":"dbSNP","id":"rs1799594971","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603567,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140603567,"clinical_significance":[],"seq_region_name":"7","id":"rs1274769722"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799595061","alleles":["A","C","G","T"],"end":140603568,"feature_type":"variation","strand":1,"source":"dbSNP","start":140603568,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799595188","source":"dbSNP","start":140603571,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140603571,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1585738402","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603576,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140603576},{"strand":1,"feature_type":"variation","end":140603583,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603583,"source":"dbSNP","seq_region_name":"7","id":"rs1002637211","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603585,"source":"dbSNP","strand":1,"feature_type":"variation","end":140603585,"alleles":["T","C","G"],"seq_region_name":"7","id":"rs1799595482","clinical_significance":[]},{"clinical_significance":[],"id":"rs1350462955","seq_region_name":"7","source":"dbSNP","start":140603587,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140603587,"alleles":["T","C"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603588,"feature_type":"variation","strand":1,"end":140603588,"alleles":["T","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs551231168"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1209241399","feature_type":"variation","strand":1,"end":140603591,"alleles":["A","C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603591},{"alleles":["G","A"],"end":140603592,"feature_type":"variation","strand":1,"source":"dbSNP","start":140603592,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs4726962"},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140603593,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603593,"source":"dbSNP","seq_region_name":"7","id":"rs978003885","clinical_significance":[]},{"id":"rs1296875631","seq_region_name":"7","clinical_significance":[],"start":140603595,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140603595,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1799596241","clinical_significance":[],"start":140603602,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140603602,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1280222582","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603610,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140603610},{"seq_region_name":"7","id":"rs1799596457","clinical_significance":[],"end":140603611,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140603611,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603627,"feature_type":"variation","strand":1,"end":140603627,"alleles":["T","A"],"clinical_significance":[],"id":"rs928349673","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799596656","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603632,"source":"dbSNP","strand":1,"feature_type":"variation","end":140603632,"alleles":["G","T"]},{"clinical_significance":[],"id":"rs1799596771","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140603633,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603633},{"end":140603634,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140603634,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130690684"},{"end":140603635,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140603635,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1799596856","seq_region_name":"7","clinical_significance":[]},{"end":140603638,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140603638,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs938433317","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140603639,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603639,"source":"dbSNP","id":"rs1799597065","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140603641,"alleles":["G","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603641,"clinical_significance":[],"seq_region_name":"7","id":"rs750730137"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799597294","alleles":["C","A"],"end":140603643,"feature_type":"variation","strand":1,"source":"dbSNP","start":140603643,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140603645,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140603645,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1381138799","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799597503","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140603652,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603652,"source":"dbSNP"},{"end":140603659,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140603659,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1055505877"},{"alleles":["A","C"],"end":140603660,"strand":1,"feature_type":"variation","start":140603660,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1799597716","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1448140199","clinical_significance":[],"start":140603669,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140603669,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140603671,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140603671,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs894135233"},{"seq_region_name":"7","id":"rs763326655","clinical_significance":[],"alleles":["G","A"],"end":140603672,"strand":1,"feature_type":"variation","start":140603672,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1389625552","end":140603681,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140603681,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["A","G"],"end":140603688,"feature_type":"variation","strand":1,"source":"dbSNP","start":140603688,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799598117"},{"end":140603689,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140603689,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799598204","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603691,"feature_type":"variation","strand":1,"end":140603691,"alleles":["C","G"],"clinical_significance":[],"id":"rs1195331507","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1585738571","seq_region_name":"7","feature_type":"variation","strand":1,"end":140603692,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603692},{"alleles":["A","G"],"end":140603694,"feature_type":"variation","strand":1,"source":"dbSNP","start":140603694,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs73736638"},{"seq_region_name":"7","id":"rs1799598627","clinical_significance":[],"end":140603696,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140603696,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs2130690797","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140603698,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603698,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140603700,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603700,"clinical_significance":[],"seq_region_name":"7","id":"rs1799598735"},{"seq_region_name":"7","id":"rs1475181676","clinical_significance":[],"end":140603701,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140603701,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603702,"feature_type":"variation","strand":1,"end":140603702,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799598929"},{"alleles":["G","-"],"end":140603711,"feature_type":"variation","strand":1,"source":"dbSNP","start":140603711,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1192029786"},{"feature_type":"variation","strand":1,"end":140603711,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603711,"clinical_significance":[],"seq_region_name":"7","id":"rs1426047173"},{"clinical_significance":[],"id":"rs1799599240","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140603714,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603714},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603719,"feature_type":"variation","strand":1,"alleles":["CTATCTA","CTA"],"end":140603725,"clinical_significance":[],"id":"rs769271497","seq_region_name":"7"},{"end":140603721,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140603721,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1181595155"},{"seq_region_name":"7","id":"rs1799599540","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603722,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140603722},{"seq_region_name":"7","id":"rs1799599639","clinical_significance":[],"start":140603723,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140603723,"alleles":["C","G","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs776407439","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603729,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140603729},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140603736,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603736,"clinical_significance":[],"seq_region_name":"7","id":"rs1799599822"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603737,"source":"dbSNP","strand":1,"feature_type":"variation","end":140603737,"alleles":["A","C"],"seq_region_name":"7","id":"rs1585738643","clinical_significance":[]},{"id":"rs1252170408","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140603741,"strand":1,"feature_type":"variation","start":140603741,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1799600081","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603742,"source":"dbSNP","strand":1,"feature_type":"variation","end":140603742,"alleles":["C","A"]},{"seq_region_name":"7","id":"rs1585738680","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603746,"source":"dbSNP","strand":1,"feature_type":"variation","end":140603746,"alleles":["A","G"]},{"clinical_significance":[],"id":"rs1206852938","seq_region_name":"7","feature_type":"variation","strand":1,"end":140603747,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603747},{"seq_region_name":"7","id":"rs1004015207","clinical_significance":[],"strand":1,"feature_type":"variation","end":140603748,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603748,"source":"dbSNP"},{"start":140603754,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140603754,"alleles":["A","T"],"strand":1,"feature_type":"variation","id":"rs1273255363","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130690926","feature_type":"variation","strand":1,"alleles":["TTTAACCTT","TT"],"end":140603763,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603755},{"start":140603763,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C","G"],"end":140603763,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs759233435","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1310317778","feature_type":"variation","strand":1,"end":140603764,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603764},{"seq_region_name":"7","id":"rs1395179674","clinical_significance":[],"strand":1,"feature_type":"variation","end":140603768,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603768,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1402381894","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140603771,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603771,"source":"dbSNP"},{"start":140603772,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140603772,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1315539566","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603773,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140603773,"seq_region_name":"7","id":"rs1408196631","clinical_significance":[]},{"id":"rs1344121045","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140603777,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603777,"source":"dbSNP"},{"id":"rs1294135942","seq_region_name":"7","clinical_significance":[],"alleles":["A","C"],"end":140603787,"strand":1,"feature_type":"variation","start":140603787,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140603788,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603788,"clinical_significance":[],"id":"rs1563172976","seq_region_name":"7"},{"start":140603791,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140603791,"strand":1,"feature_type":"variation","id":"rs1459922771","seq_region_name":"7","clinical_significance":[]},{"start":140603792,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140603792,"strand":1,"feature_type":"variation","id":"rs530432556","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1367161599","clinical_significance":[],"alleles":["A","G"],"end":140603795,"strand":1,"feature_type":"variation","start":140603795,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140603796,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603796,"clinical_significance":[],"id":"rs1164680786","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1473163761","seq_region_name":"7","end":140603797,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140603797,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585738842","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603799,"feature_type":"variation","strand":1,"end":140603799,"alleles":["A","C"]},{"end":140603800,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140603800,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs75391852"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1489009313","feature_type":"variation","strand":1,"end":140603801,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603801},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603802,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140603802,"seq_region_name":"7","id":"rs1183963030","clinical_significance":[]},{"id":"rs1799602467","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140603806,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603806,"source":"dbSNP"},{"end":140603809,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140603809,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1481841988"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603811,"source":"dbSNP","strand":1,"feature_type":"variation","end":140603811,"alleles":["T","A","C"],"seq_region_name":"7","id":"rs186557822","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140603814,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603814,"clinical_significance":[],"seq_region_name":"7","id":"rs1799602812"},{"feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140603821,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603821,"clinical_significance":[],"seq_region_name":"7","id":"rs751711137"},{"seq_region_name":"7","id":"rs534954484","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140603828,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603828,"source":"dbSNP"},{"start":140603829,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140603829,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs910723113","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603832,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140603832,"clinical_significance":[],"seq_region_name":"7","id":"rs755203198"},{"clinical_significance":[],"id":"rs1243970904","seq_region_name":"7","end":140603837,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140603837,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1329651855","clinical_significance":[],"start":140603839,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140603839,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603841,"feature_type":"variation","strand":1,"end":140603841,"alleles":["A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799603636"},{"feature_type":"variation","strand":1,"end":140603842,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603842,"clinical_significance":[],"seq_region_name":"7","id":"rs1368406254"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1289955703","alleles":["G","A"],"end":140603843,"feature_type":"variation","strand":1,"source":"dbSNP","start":140603843,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799604007","alleles":["C","T"],"end":140603848,"feature_type":"variation","strand":1,"source":"dbSNP","start":140603848,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140603849,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140603849,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799604118"},{"seq_region_name":"7","id":"rs1226817808","clinical_significance":[],"alleles":["G","A"],"end":140603850,"strand":1,"feature_type":"variation","start":140603850,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["C","T"],"end":140603853,"feature_type":"variation","strand":1,"source":"dbSNP","start":140603853,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799604344","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140603857,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603857,"source":"dbSNP","id":"rs1585738944","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799604542","seq_region_name":"7","end":140603860,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140603860,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1585738953","seq_region_name":"7","clinical_significance":[],"start":140603861,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140603861,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs953338461","clinical_significance":[],"strand":1,"feature_type":"variation","end":140603862,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603862,"source":"dbSNP"},{"source":"dbSNP","start":140603863,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140603863,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585738970"},{"id":"rs1799604962","seq_region_name":"7","clinical_significance":[],"end":140603877,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140603877,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140603878,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603878,"source":"dbSNP","seq_region_name":"7","id":"rs1585738983","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140603882,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603882,"clinical_significance":[],"seq_region_name":"7","id":"rs1799605196"},{"clinical_significance":[],"id":"rs2130691204","seq_region_name":"7","end":140603886,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140603886,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140603887,"alleles":["T","C","G"],"strand":1,"feature_type":"variation","start":140603887,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs990572726","clinical_significance":[]},{"end":140603891,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140603891,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1232541596","seq_region_name":"7"},{"start":140603894,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140603894,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130691227","clinical_significance":[]},{"start":140603900,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140603900,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799605483","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140603903,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603903,"clinical_significance":[],"id":"rs1799605571","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563173031","feature_type":"variation","strand":1,"end":140603906,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603906},{"clinical_significance":[],"seq_region_name":"7","id":"rs1388660695","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140603909,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603909},{"alleles":["T","C","G"],"end":140603911,"feature_type":"variation","strand":1,"source":"dbSNP","start":140603911,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1021847287"},{"strand":1,"feature_type":"variation","end":140603914,"alleles":["-","CATAT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603915,"source":"dbSNP","id":"rs1351950681","seq_region_name":"7","clinical_significance":[]},{"end":140603919,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140603919,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799606008","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1054203300","feature_type":"variation","strand":1,"end":140603922,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603922},{"end":140603925,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140603925,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799606261"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603929,"feature_type":"variation","strand":1,"end":140603929,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs968039192"},{"seq_region_name":"7","id":"rs1471409021","clinical_significance":[],"strand":1,"feature_type":"variation","end":140603935,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603935,"source":"dbSNP"},{"id":"rs1362800329","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140603938,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603938,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799606668","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603944,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140603944},{"clinical_significance":[],"id":"rs553285495","seq_region_name":"7","source":"dbSNP","start":140603947,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140603947,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140603949,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603949,"clinical_significance":[],"id":"rs2130691307","seq_region_name":"7"},{"clinical_significance":[],"id":"rs571514609","seq_region_name":"7","source":"dbSNP","start":140603953,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140603953,"alleles":["T","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1799606964","clinical_significance":[],"start":140603956,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140603956,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"end":140603957,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140603957,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799607078","clinical_significance":[]},{"id":"rs1199116318","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603962,"source":"dbSNP","strand":1,"feature_type":"variation","end":140603962,"alleles":["G","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs977743070","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140603965,"feature_type":"variation","strand":1,"end":140603965,"alleles":["A","C"]},{"end":140603967,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140603967,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799607365","clinical_significance":[]},{"seq_region_name":"7","id":"rs1264614799","clinical_significance":[],"strand":1,"feature_type":"variation","end":140603968,"alleles":["A","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603968,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603969,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C","T"],"end":140603969,"seq_region_name":"7","id":"rs28413042","clinical_significance":[]},{"alleles":["T","C"],"end":140603974,"feature_type":"variation","strand":1,"source":"dbSNP","start":140603974,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs938883681"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603978,"source":"dbSNP","strand":1,"feature_type":"variation","end":140603978,"alleles":["T","C"],"seq_region_name":"7","id":"rs991181614","clinical_significance":[]},{"seq_region_name":"7","id":"rs567114843","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140603985,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603985,"source":"dbSNP"},{"id":"rs2130691373","seq_region_name":"7","clinical_significance":[],"start":140603985,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AAAAA","AAAA"],"end":140603989,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140603986,"source":"dbSNP","strand":1,"feature_type":"variation","end":140603986,"alleles":["A","G"],"seq_region_name":"7","id":"rs1799608172","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1206513417","alleles":["A","G"],"end":140603987,"feature_type":"variation","strand":1,"source":"dbSNP","start":140603987,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140603989,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140603989,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1328765696","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799608446","clinical_significance":[],"alleles":["A","G"],"end":140603991,"strand":1,"feature_type":"variation","start":140603991,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140603997,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AAA","AA"],"end":140603999,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799608547"},{"clinical_significance":[],"id":"rs1192705124","seq_region_name":"7","source":"dbSNP","start":140604009,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140604009,"alleles":["C","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs190479165","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140604016,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140604016,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1055996521","end":140604018,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140604018,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1329470903","seq_region_name":"7","clinical_significance":[],"start":140604026,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140604026,"alleles":["G","A","C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs894307416","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140604030,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140604030},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604039,"feature_type":"variation","strand":1,"end":140604039,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799609211"},{"seq_region_name":"7","id":"rs1471096455","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140604043,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140604043,"source":"dbSNP"},{"end":140604045,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140604045,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799609420"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799609515","end":140604046,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140604046,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140604053,"alleles":["C","A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140604053,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1156710756","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140604056,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604056,"clinical_significance":[],"seq_region_name":"7","id":"rs1585739336"},{"seq_region_name":"7","id":"rs1799609848","clinical_significance":[],"strand":1,"feature_type":"variation","end":140604061,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140604061,"source":"dbSNP"},{"id":"rs548658607","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140604072,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140604072},{"clinical_significance":[],"id":"rs1799610170","seq_region_name":"7","alleles":["C","T"],"end":140604076,"feature_type":"variation","strand":1,"source":"dbSNP","start":140604076,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1367888958","alleles":["A","G"],"end":140604077,"feature_type":"variation","strand":1,"source":"dbSNP","start":140604077,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["G","A"],"end":140604080,"feature_type":"variation","strand":1,"source":"dbSNP","start":140604080,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799610358"},{"feature_type":"variation","strand":1,"end":140604085,"alleles":["TTT","TT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604083,"clinical_significance":[],"id":"rs1799610444","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140604088,"source":"dbSNP","strand":1,"feature_type":"variation","end":140604088,"alleles":["A","G"],"seq_region_name":"7","id":"rs542677243","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140604094,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140604094,"id":"rs183023448","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs572885801","end":140604095,"alleles":["G","A","C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140604095,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1585739390","clinical_significance":[],"strand":1,"feature_type":"variation","end":140604105,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140604105,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs962146021","alleles":["C","T"],"end":140604107,"feature_type":"variation","strand":1,"source":"dbSNP","start":140604107,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1799611204","clinical_significance":[],"start":140604111,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140604111,"alleles":["T","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs540552619","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140604114,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140604114,"source":"dbSNP"},{"source":"dbSNP","start":140604115,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140604115,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585739423"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604119,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140604119,"clinical_significance":[],"seq_region_name":"7","id":"rs900993172"},{"seq_region_name":"7","id":"rs1799611679","clinical_significance":[],"start":140604120,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140604120,"strand":1,"feature_type":"variation"},{"alleles":["T","G"],"end":140604126,"strand":1,"feature_type":"variation","start":140604126,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs996704057","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140604128,"source":"dbSNP","strand":1,"feature_type":"variation","end":140604128,"alleles":["T","G"],"seq_region_name":"7","id":"rs1799611901","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799612062","end":140604132,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140604132,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1799612145","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["-","ATAC"],"end":140604132,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140604133,"source":"dbSNP"},{"id":"rs1249746405","seq_region_name":"7","clinical_significance":[],"end":140604135,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140604135,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799612327","feature_type":"variation","strand":1,"alleles":["T","A"],"end":140604136,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604136},{"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140604137,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140604137,"source":"dbSNP","id":"rs1799612422","seq_region_name":"7","clinical_significance":[]},{"id":"rs1186594350","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140604138,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140604138,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1446258569","source":"dbSNP","start":140604140,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140604140,"alleles":["T","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs954900692","clinical_significance":[],"start":140604146,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G","T"],"end":140604146,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs565232072","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604147,"feature_type":"variation","strand":1,"end":140604147,"alleles":["G","A"]},{"end":140604149,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140604149,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs889216370","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140604150,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140604150,"seq_region_name":"7","id":"rs1202424209","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1011541278","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604156,"feature_type":"variation","strand":1,"end":140604156,"alleles":["T","G"]},{"id":"rs1563173178","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140604157,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140604157},{"clinical_significance":[],"seq_region_name":"7","id":"rs186192518","feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140604158,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604158},{"alleles":["G","C"],"end":140604160,"feature_type":"variation","strand":1,"source":"dbSNP","start":140604160,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799613164"},{"start":140604161,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140604161,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799613258","clinical_significance":[]},{"alleles":["C","T"],"end":140604164,"feature_type":"variation","strand":1,"source":"dbSNP","start":140604164,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs17161636","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1585739562","clinical_significance":[],"end":140604167,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140604167,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs2130691699","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140604170,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604170},{"alleles":["A","G"],"end":140604172,"strand":1,"feature_type":"variation","start":140604172,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585739570","clinical_significance":[]},{"id":"rs745826828","seq_region_name":"7","clinical_significance":[],"start":140604173,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140604173,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"end":140604174,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140604174,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585739586","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799613884","end":140604179,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140604179,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140604180,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140604180,"seq_region_name":"7","id":"rs990078866","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140604181,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140604181,"source":"dbSNP","id":"rs1233978707","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140604182,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140604182,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs978066072","seq_region_name":"7"},{"start":140604183,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140604183,"alleles":["T","C","G"],"strand":1,"feature_type":"variation","id":"rs1799614295","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140604186,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140604186,"source":"dbSNP","seq_region_name":"7","id":"rs1397445831","clinical_significance":[]},{"seq_region_name":"7","id":"rs1399526925","clinical_significance":[],"start":140604187,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140604187,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140604188,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140604188,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1035929433"},{"seq_region_name":"7","id":"rs1041332113","clinical_significance":[],"end":140604190,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","start":140604190,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs928307033","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140604193,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140604193,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140604194,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604194,"clinical_significance":[],"seq_region_name":"7","id":"rs1799614922"},{"seq_region_name":"7","id":"rs1213330978","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140604197,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140604197,"source":"dbSNP"},{"source":"dbSNP","start":140604201,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140604201,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799615099"},{"feature_type":"variation","strand":1,"end":140604202,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604202,"clinical_significance":[],"seq_region_name":"7","id":"rs1799615220"},{"clinical_significance":[],"id":"rs1475016433","seq_region_name":"7","source":"dbSNP","start":140604207,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140604207,"alleles":["C","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1799615404","clinical_significance":[],"strand":1,"feature_type":"variation","end":140604209,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140604209,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs563238806","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140604212,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604212},{"seq_region_name":"7","id":"rs1251561414","clinical_significance":[],"start":140604218,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140604218,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130691827","end":140604222,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140604222,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140604224,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140604224,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1554479129","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1439313608","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140604228,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604228},{"clinical_significance":[],"id":"rs1440922927","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140604232,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604232},{"id":"rs1799616251","seq_region_name":"7","clinical_significance":[],"alleles":["A","T"],"end":140604235,"strand":1,"feature_type":"variation","start":140604235,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1179463433","end":140604238,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140604238,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799616507","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604239,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140604239},{"clinical_significance":[],"seq_region_name":"7","id":"rs991631489","feature_type":"variation","strand":1,"end":140604241,"alleles":["A","C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604241},{"start":140604247,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140604247,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799616771","clinical_significance":[]},{"source":"dbSNP","start":140604251,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140604251,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs74496562"},{"clinical_significance":[],"seq_region_name":"7","id":"rs952573040","source":"dbSNP","start":140604254,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140604254,"feature_type":"variation","strand":1},{"start":140604261,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140604261,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs549084966","clinical_significance":[]},{"seq_region_name":"7","id":"rs797000089","clinical_significance":[],"alleles":["C","T"],"end":140604263,"strand":1,"feature_type":"variation","start":140604263,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140604266,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140604266,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs571383169","seq_region_name":"7"},{"alleles":["A","G"],"end":140604270,"feature_type":"variation","strand":1,"source":"dbSNP","start":140604270,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs894414399"},{"alleles":["G","T"],"end":140604271,"feature_type":"variation","strand":1,"source":"dbSNP","start":140604271,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799617526"},{"alleles":["G","A"],"end":140604274,"strand":1,"feature_type":"variation","start":140604274,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1166394317","clinical_significance":[]},{"id":"rs1286324407","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140604276,"source":"dbSNP","strand":1,"feature_type":"variation","end":140604276,"alleles":["G","A"]},{"end":140604280,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140604280,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs983925880","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1037958787","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140604292,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140604292},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604295,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140604295,"clinical_significance":[],"seq_region_name":"7","id":"rs908195590"},{"clinical_significance":[],"seq_region_name":"7","id":"rs190996317","feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140604296,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604296},{"clinical_significance":[],"seq_region_name":"7","id":"rs993582897","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604298,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140604298},{"alleles":["T","A"],"end":140604306,"feature_type":"variation","strand":1,"source":"dbSNP","start":140604306,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799618300"},{"source":"dbSNP","start":140604308,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140604308,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1398245599"},{"start":140604314,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140604314,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1414367029","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140604315,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140604315,"seq_region_name":"7","id":"rs2130691994","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130691999","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140604316,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140604316},{"clinical_significance":[],"id":"rs1799618598","seq_region_name":"7","alleles":["C","T"],"end":140604318,"feature_type":"variation","strand":1,"source":"dbSNP","start":140604318,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1030457327","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604331,"feature_type":"variation","strand":1,"end":140604331,"alleles":["C","T"]},{"strand":1,"feature_type":"variation","end":140604333,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140604333,"source":"dbSNP","id":"rs1799618798","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604334,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140604334,"clinical_significance":[],"seq_region_name":"7","id":"rs890451812"},{"seq_region_name":"7","id":"rs528093275","clinical_significance":[],"end":140604335,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140604335,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140604336,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140604336,"source":"dbSNP","id":"rs1040963057","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","T"],"end":140604341,"strand":1,"feature_type":"variation","start":140604341,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs922529736","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1327354149","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140604342,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604342},{"alleles":["A","G"],"end":140604346,"feature_type":"variation","strand":1,"source":"dbSNP","start":140604346,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs75074533"},{"feature_type":"variation","strand":1,"end":140604348,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604348,"clinical_significance":[],"seq_region_name":"7","id":"rs78782193"},{"clinical_significance":[],"id":"rs386718483","seq_region_name":"7","end":140604350,"alleles":["ACA","CCG"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140604348,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1799619814","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604349,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140604349},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604350,"feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140604350,"clinical_significance":[],"seq_region_name":"7","id":"rs75496458"},{"start":140604350,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","-"],"end":140604350,"strand":1,"feature_type":"variation","id":"rs1295155092","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140604351,"source":"dbSNP","strand":1,"feature_type":"variation","end":140604357,"alleles":["TTTTTTT","TTTTTTTT"],"id":"rs989634364","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140604353,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140604353,"source":"dbSNP","seq_region_name":"7","id":"rs1012068585","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140604358,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604358,"clinical_significance":[],"id":"rs977139696","seq_region_name":"7"},{"source":"dbSNP","start":140604359,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140604359,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799620469"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1228664079","alleles":["A","G"],"end":140604367,"feature_type":"variation","strand":1,"source":"dbSNP","start":140604367,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1351882187","source":"dbSNP","start":140604382,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140604382,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140604383,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140604383,"source":"dbSNP","seq_region_name":"7","id":"rs1799620808","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130692126","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140604384,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140604384},{"seq_region_name":"7","id":"rs1043178304","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140604387,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140604387},{"start":140604390,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140604389,"alleles":["-","TTATTTAA"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799621021","clinical_significance":[]},{"id":"rs1799621120","seq_region_name":"7","clinical_significance":[],"start":140604393,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140604393,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1799621209","clinical_significance":[],"end":140604395,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140604395,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140604396,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140604396,"source":"dbSNP","seq_region_name":"7","id":"rs1799621319","clinical_significance":[]},{"clinical_significance":[],"id":"rs1277280846","seq_region_name":"7","source":"dbSNP","start":140604403,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140604403,"alleles":["T","A"],"feature_type":"variation","strand":1},{"id":"rs1440915626","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140604409,"source":"dbSNP","strand":1,"feature_type":"variation","end":140604409,"alleles":["T","C"]},{"start":140604411,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140604411,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799621632","clinical_significance":[]},{"seq_region_name":"7","id":"rs183358184","clinical_significance":[],"end":140604414,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140604414,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799621851","feature_type":"variation","strand":1,"alleles":["T","-"],"end":140604415,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604415},{"seq_region_name":"7","id":"rs1325490591","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140604419,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140604419,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799622076","clinical_significance":[],"alleles":["AATTA","A"],"end":140604424,"strand":1,"feature_type":"variation","start":140604420,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["A","G"],"end":140604421,"feature_type":"variation","strand":1,"source":"dbSNP","start":140604421,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs998830596"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799622275","alleles":["G","C"],"end":140604425,"feature_type":"variation","strand":1,"source":"dbSNP","start":140604425,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604428,"feature_type":"variation","strand":1,"end":140604428,"alleles":["T","C"],"clinical_significance":[],"id":"rs1799622379","seq_region_name":"7"},{"id":"rs2130692224","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140604431,"strand":1,"feature_type":"variation","start":140604431,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140604436,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140604436,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1252093633","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1403513236","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140604438,"source":"dbSNP","strand":1,"feature_type":"variation","end":140604438,"alleles":["T","C"]},{"clinical_significance":[],"id":"rs1799622709","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604442,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140604442},{"source":"dbSNP","start":140604446,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140604446,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1341808784","seq_region_name":"7"},{"start":140604447,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140604447,"alleles":["A","G"],"strand":1,"feature_type":"variation","id":"rs142315184","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799623021","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140604449,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604449},{"start":140604452,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140604452,"alleles":["G","A","C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799623111","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140604455,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140604455,"source":"dbSNP","id":"rs1393482469","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799623347","clinical_significance":[],"start":140604463,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140604463,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140604469,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140604469,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799623441"},{"clinical_significance":[],"seq_region_name":"7","id":"rs187485531","end":140604471,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140604471,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604474,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140604474,"clinical_significance":[],"seq_region_name":"7","id":"rs1385091"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604475,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140604475,"clinical_significance":[],"id":"rs1799623742","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1035875873","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140604486,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604486},{"clinical_significance":[],"id":"rs2130692334","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604488,"feature_type":"variation","strand":1,"end":140604488,"alleles":["T","C"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604490,"feature_type":"variation","strand":1,"end":140604490,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799623949"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799624057","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140604492,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604492},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140604496,"source":"dbSNP","strand":1,"feature_type":"variation","end":140604496,"alleles":["T","C"],"seq_region_name":"7","id":"rs960289185","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1013000272","end":140604499,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140604499,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140604502,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C","G"],"end":140604502,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585740153"},{"seq_region_name":"7","id":"rs1799624504","clinical_significance":[],"start":140604513,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140604513,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130692372","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604514,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140604514},{"seq_region_name":"7","id":"rs1563173352","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140604518,"source":"dbSNP","strand":1,"feature_type":"variation","end":140604518,"alleles":["T","G"]},{"seq_region_name":"7","id":"rs1799624729","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140604522,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140604522},{"clinical_significance":[],"seq_region_name":"7","id":"rs915808429","source":"dbSNP","start":140604526,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140604526,"alleles":["T","C"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140604529,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140604529,"seq_region_name":"7","id":"rs1799624931","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130692406","feature_type":"variation","strand":1,"end":140604530,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604530},{"end":140604532,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140604532,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1799625031","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs76016784","clinical_significance":[],"end":140604539,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140604539,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140604540,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604540,"clinical_significance":[],"seq_region_name":"7","id":"rs1799625268"},{"clinical_significance":[],"id":"rs1248508896","seq_region_name":"7","end":140604542,"alleles":["GTT","GTTGTT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140604540,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1799625468","seq_region_name":"7","clinical_significance":[],"end":140604549,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140604549,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140604555,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140604555,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1037507361"},{"clinical_significance":[],"id":"rs1468399549","seq_region_name":"7","source":"dbSNP","start":140604557,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140604557,"alleles":["G","A"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140604563,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604563,"clinical_significance":[],"id":"rs1799625732","seq_region_name":"7"},{"alleles":["C","T"],"end":140604568,"feature_type":"variation","strand":1,"source":"dbSNP","start":140604568,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs952942715","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140604572,"alleles":["CTCTC","CTCTCTC"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604568,"clinical_significance":[],"seq_region_name":"7","id":"rs1799625945"},{"seq_region_name":"7","id":"rs1249572953","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140604575,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140604575,"source":"dbSNP"},{"source":"dbSNP","start":140604584,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140604584,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1210912134"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130692486","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604585,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140604585},{"clinical_significance":[],"id":"rs929155384","seq_region_name":"7","end":140604591,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140604591,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140604594,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AGAGAGAG","AGAG","AGAGAG"],"end":140604601,"seq_region_name":"7","id":"rs1485929438","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs192736759","source":"dbSNP","start":140604595,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140604595,"alleles":["G","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1367753236","clinical_significance":[],"start":140604597,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140604597,"strand":1,"feature_type":"variation"},{"start":140604598,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","AA"],"end":140604598,"strand":1,"feature_type":"variation","id":"rs1799626697","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140604602,"source":"dbSNP","strand":1,"feature_type":"variation","end":140604609,"alleles":["GACAGACA","GACA"],"seq_region_name":"7","id":"rs1276058353","clinical_significance":[]},{"seq_region_name":"7","id":"rs1438660954","clinical_significance":[],"start":140604605,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140604605,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs984264237","feature_type":"variation","strand":1,"end":140604610,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604610},{"clinical_significance":[],"seq_region_name":"7","id":"rs1370072549","end":140604617,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140604617,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140604618,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604618,"clinical_significance":[],"seq_region_name":"7","id":"rs1563173389"},{"start":140604627,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140604627,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799628075","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130692551","clinical_significance":[],"alleles":["A","G"],"end":140604630,"strand":1,"feature_type":"variation","start":140604630,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs908309806","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140604633,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140604633,"source":"dbSNP"},{"source":"dbSNP","start":140604638,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140604638,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1320990558","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1255371185","feature_type":"variation","strand":1,"end":140604640,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604640},{"clinical_significance":[],"id":"rs2130692580","seq_region_name":"7","feature_type":"variation","strand":1,"end":140604643,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604643},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604646,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140604646,"clinical_significance":[],"seq_region_name":"7","id":"rs1799628490"},{"alleles":["C","T"],"end":140604647,"strand":1,"feature_type":"variation","start":140604647,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799628594","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799628694","clinical_significance":[],"start":140604650,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140604650,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140604659,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604659,"clinical_significance":[],"seq_region_name":"7","id":"rs961308220"},{"seq_region_name":"7","id":"rs976426164","clinical_significance":[],"strand":1,"feature_type":"variation","end":140604662,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140604662,"source":"dbSNP"},{"source":"dbSNP","start":140604663,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140604663,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1474582573"},{"source":"dbSNP","start":140604664,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140604664,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1158699370"},{"alleles":["C","G"],"end":140604666,"strand":1,"feature_type":"variation","start":140604666,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1415211793","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140604672,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140604672,"source":"dbSNP","seq_region_name":"7","id":"rs1293611112","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1189484743","alleles":["G","A"],"end":140604673,"feature_type":"variation","strand":1,"source":"dbSNP","start":140604673,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1799629534","clinical_significance":[],"end":140604676,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140604676,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140604678,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140604678,"source":"dbSNP","seq_region_name":"7","id":"rs572948764","clinical_significance":[]},{"start":140604681,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140604681,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs932556832","clinical_significance":[]},{"end":140604684,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140604684,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799629886"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1249255637","source":"dbSNP","start":140604685,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140604685,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1007535433","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140604687,"source":"dbSNP","strand":1,"feature_type":"variation","end":140604687,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1367013036","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140604690,"source":"dbSNP","strand":1,"feature_type":"variation","end":140604690,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799630341","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604693,"feature_type":"variation","strand":1,"end":140604693,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799630433","source":"dbSNP","start":140604694,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140604694,"alleles":["G","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1049708565","clinical_significance":[],"start":140604698,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140604698,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604699,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140604699,"clinical_significance":[],"seq_region_name":"7","id":"rs769209140"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1011579225","source":"dbSNP","start":140604701,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140604701,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140604702,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140604702,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585740464"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1021202661","end":140604712,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140604712,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1280130558","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140604717,"source":"dbSNP","strand":1,"feature_type":"variation","end":140604717,"alleles":["A","G"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140604718,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140604718,"seq_region_name":"7","id":"rs1799631165","clinical_significance":[]},{"end":140604723,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140604723,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs966842540","seq_region_name":"7"},{"id":"rs1346498200","seq_region_name":"7","clinical_significance":[],"start":140604726,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140604726,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799631518","feature_type":"variation","strand":1,"end":140604728,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604728},{"seq_region_name":"7","id":"rs1370362554","clinical_significance":[],"start":140604730,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140604730,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604740,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140604740,"clinical_significance":[],"id":"rs533920578","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1435844249","feature_type":"variation","strand":1,"end":140604746,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604746},{"id":"rs1799631932","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140604746,"source":"dbSNP","strand":1,"feature_type":"variation","end":140604759,"alleles":["GACTTGAGACTTGA","GACTTGA"]},{"id":"rs558831046","seq_region_name":"7","clinical_significance":[],"start":140604748,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140604748,"alleles":["C","A","G"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140604755,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140604755,"source":"dbSNP","seq_region_name":"7","id":"rs1799632197","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140604760,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140604760,"seq_region_name":"7","id":"rs1799632296","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799632410","clinical_significance":[],"start":140604762,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140604762,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs756283778","clinical_significance":[],"start":140604764,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140604764,"strand":1,"feature_type":"variation"},{"start":140604769,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140604769,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs182792163","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1414237974","source":"dbSNP","start":140604775,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140604775,"alleles":["T","C"],"feature_type":"variation","strand":1},{"start":140604777,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140604777,"alleles":["T","C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1171994720","clinical_significance":[]},{"source":"dbSNP","start":140604779,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140604779,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799632998"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1390833095","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604785,"feature_type":"variation","strand":1,"end":140604785,"alleles":["G","A"]},{"source":"dbSNP","start":140604789,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140604789,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799633113"},{"id":"rs544498691","seq_region_name":"7","clinical_significance":[],"start":140604790,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140604790,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1171093864","feature_type":"variation","strand":1,"end":140604792,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604792},{"seq_region_name":"7","id":"rs1799633466","clinical_significance":[],"start":140604793,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AAA","AA"],"end":140604795,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1799633600","seq_region_name":"7","end":140604796,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140604796,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1448149362","source":"dbSNP","start":140604800,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140604800,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604802,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140604802,"clinical_significance":[],"seq_region_name":"7","id":"rs1261508985"},{"start":140604804,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140604804,"alleles":["G","C"],"strand":1,"feature_type":"variation","id":"rs1799633909","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1296385468","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140604811,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140604811},{"seq_region_name":"7","id":"rs1799634107","clinical_significance":[],"end":140604812,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140604812,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799634223","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604813,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140604813},{"seq_region_name":"7","id":"rs1799634321","clinical_significance":[],"strand":1,"feature_type":"variation","end":140604815,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140604815,"source":"dbSNP"},{"id":"rs1799634442","seq_region_name":"7","clinical_significance":[],"alleles":["TATT","T"],"end":140604824,"strand":1,"feature_type":"variation","start":140604821,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["A","G"],"end":140604822,"strand":1,"feature_type":"variation","start":140604822,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1182738139","clinical_significance":[]},{"id":"rs1799634673","seq_region_name":"7","clinical_significance":[],"start":140604825,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140604825,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"start":140604829,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140604829,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1483380179","clinical_significance":[]},{"alleles":["G","A"],"end":140604832,"strand":1,"feature_type":"variation","start":140604832,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799634870","clinical_significance":[]},{"seq_region_name":"7","id":"rs1238899392","clinical_significance":[],"alleles":["G","A"],"end":140604839,"strand":1,"feature_type":"variation","start":140604839,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1208269132","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140604840,"source":"dbSNP","strand":1,"feature_type":"variation","end":140604840,"alleles":["T","C"]},{"source":"dbSNP","start":140604841,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140604841,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs960079817"},{"seq_region_name":"7","id":"rs1799635296","clinical_significance":[],"alleles":["A","G"],"end":140604843,"strand":1,"feature_type":"variation","start":140604843,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1799635396","clinical_significance":[],"end":140604844,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140604844,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs563134604","seq_region_name":"7","feature_type":"variation","strand":1,"end":140604849,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604849},{"end":140604852,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140604852,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799635602"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799635703","end":140604853,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140604853,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604854,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140604854,"clinical_significance":[],"id":"rs1043513716","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140604868,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604868,"clinical_significance":[],"seq_region_name":"7","id":"rs1799635812"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604871,"feature_type":"variation","strand":1,"alleles":["AATGAATGAATGAAT","AATGAATGAATGAATGAAT"],"end":140604885,"clinical_significance":[],"seq_region_name":"7","id":"rs1799635910"},{"clinical_significance":[],"id":"rs74709584","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604872,"feature_type":"variation","strand":1,"end":140604872,"alleles":["A","C"]},{"seq_region_name":"7","id":"rs773726304","clinical_significance":[],"alleles":["T","C"],"end":140604873,"strand":1,"feature_type":"variation","start":140604873,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140604878,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604878,"clinical_significance":[],"id":"rs1799636246","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1250510832","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140604880,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604880},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140604884,"source":"dbSNP","strand":1,"feature_type":"variation","end":140604884,"alleles":["A","C","G"],"seq_region_name":"7","id":"rs1348284073","clinical_significance":[]},{"end":140604890,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140604890,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs763372109","clinical_significance":[]},{"end":140604896,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140604896,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs998779512"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140604897,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140604897,"seq_region_name":"7","id":"rs1799636856","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140604901,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604901,"clinical_significance":[],"seq_region_name":"7","id":"rs1212818655"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140604903,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140604903,"seq_region_name":"7","id":"rs766706239","clinical_significance":[]},{"alleles":["G","A"],"end":140604905,"strand":1,"feature_type":"variation","start":140604905,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1057064173","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1414377125","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604910,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140604910},{"clinical_significance":[],"seq_region_name":"7","id":"rs1278085392","alleles":["T","C"],"end":140604915,"feature_type":"variation","strand":1,"source":"dbSNP","start":140604915,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140604916,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140604916,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1563173521"},{"source":"dbSNP","start":140604917,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140604917,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs895861707"},{"clinical_significance":[],"id":"rs1013112749","seq_region_name":"7","source":"dbSNP","start":140604918,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C","G"],"end":140604918,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140604919,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140604919,"source":"dbSNP","seq_region_name":"7","id":"rs866093062","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140604920,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604920,"clinical_significance":[],"seq_region_name":"7","id":"rs1372949938"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1205140105","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604933,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140604933},{"clinical_significance":[],"id":"rs2130693069","seq_region_name":"7","end":140604935,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140604935,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604941,"feature_type":"variation","strand":1,"end":140604941,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs941743728"},{"seq_region_name":"7","id":"rs188458970","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140604945,"source":"dbSNP","strand":1,"feature_type":"variation","end":140604945,"alleles":["C","A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs973307034","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140604947,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604947},{"alleles":["T","C"],"end":140604959,"feature_type":"variation","strand":1,"source":"dbSNP","start":140604959,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs952973985"},{"source":"dbSNP","start":140604965,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140604965,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1005735391"},{"seq_region_name":"7","id":"rs1251916744","clinical_significance":[],"start":140604966,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140604966,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["GTAAGTA","GTA"],"end":140604972,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604966,"clinical_significance":[],"seq_region_name":"7","id":"rs1799638793"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1015728376","source":"dbSNP","start":140604970,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140604970,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799639010","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604974,"feature_type":"variation","strand":1,"end":140604974,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1479366724","alleles":["A","C"],"end":140604975,"feature_type":"variation","strand":1,"source":"dbSNP","start":140604975,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140604976,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140604976,"source":"dbSNP","seq_region_name":"7","id":"rs1250758621","clinical_significance":[]},{"id":"rs961159838","seq_region_name":"7","clinical_significance":[],"start":140604982,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140604982,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604990,"feature_type":"variation","strand":1,"end":140604990,"alleles":["G","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs976373990"},{"strand":1,"feature_type":"variation","end":140604993,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140604993,"source":"dbSNP","seq_region_name":"7","id":"rs1563173564","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604995,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140604995,"clinical_significance":[],"seq_region_name":"7","id":"rs565491155"},{"seq_region_name":"7","id":"rs1291159272","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140604997,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140604997},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140604998,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140604998,"clinical_significance":[],"seq_region_name":"7","id":"rs1799639874"},{"end":140604999,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140604999,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799639982"},{"alleles":["A","-"],"end":140605002,"strand":1,"feature_type":"variation","start":140605002,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1192068361","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799640211","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605004,"feature_type":"variation","strand":1,"end":140605004,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1232930361","end":140605007,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140605007,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140605011,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605011,"clinical_significance":[],"seq_region_name":"7","id":"rs542794183"},{"clinical_significance":[],"id":"rs1395354726","seq_region_name":"7","feature_type":"variation","strand":1,"end":140605013,"alleles":["TT","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605012},{"source":"dbSNP","start":140605022,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140605022,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1029325988"},{"clinical_significance":[],"id":"rs1799640719","seq_region_name":"7","end":140605028,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140605028,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140605030,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140605030,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799640815"},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140605032,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605032,"clinical_significance":[],"seq_region_name":"7","id":"rs1799640925"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140605033,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140605033,"source":"dbSNP","seq_region_name":"7","id":"rs1585740997","clinical_significance":[]},{"clinical_significance":[],"id":"rs192129062","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605034,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140605034},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140605035,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140605035,"source":"dbSNP","id":"rs953723824","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799641331","source":"dbSNP","start":140605036,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140605036,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140605042,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TT","-"],"end":140605043,"seq_region_name":"7","id":"rs1175988213","clinical_significance":[]},{"alleles":["T","C"],"end":140605043,"feature_type":"variation","strand":1,"source":"dbSNP","start":140605043,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130693250"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140605044,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140605044,"seq_region_name":"7","id":"rs1051614898","clinical_significance":[]},{"end":140605049,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140605049,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799641702"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605051,"feature_type":"variation","strand":1,"end":140605051,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799641800"},{"source":"dbSNP","start":140605052,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140605052,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1374101496","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605053,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140605053,"clinical_significance":[],"seq_region_name":"7","id":"rs985359061"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1164580803","source":"dbSNP","start":140605056,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["GG","G"],"end":140605057,"feature_type":"variation","strand":1},{"id":"rs1465991359","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140605057,"source":"dbSNP","strand":1,"feature_type":"variation","end":140605057,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1799642333","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140605072,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140605072},{"clinical_significance":[],"seq_region_name":"7","id":"rs1474685586","alleles":["A","C"],"end":140605076,"feature_type":"variation","strand":1,"source":"dbSNP","start":140605076,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140605077,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140605077,"source":"dbSNP","seq_region_name":"7","id":"rs1397778572","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585741081","source":"dbSNP","start":140605078,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140605078,"alleles":["A","G"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140605083,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605083,"clinical_significance":[],"id":"rs1412335619","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140605087,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605087,"clinical_significance":[],"seq_region_name":"7","id":"rs1799642798"},{"alleles":["C","G"],"end":140605088,"strand":1,"feature_type":"variation","start":140605088,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs943456580","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140605093,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605093,"clinical_significance":[],"seq_region_name":"7","id":"rs201794448"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1380642783","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605096,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140605096},{"seq_region_name":"7","id":"rs78973217","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140605097,"source":"dbSNP","strand":1,"feature_type":"variation","end":140605097,"alleles":["C","A","G","T"]},{"seq_region_name":"7","id":"rs1372077892","clinical_significance":[],"strand":1,"feature_type":"variation","end":140605098,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140605098,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605099,"feature_type":"variation","strand":1,"end":140605099,"alleles":["C","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799643499"},{"seq_region_name":"7","id":"rs1489400745","clinical_significance":[],"strand":1,"feature_type":"variation","end":140605102,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140605102,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140605106,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605106,"clinical_significance":[],"seq_region_name":"7","id":"rs1799643714"},{"clinical_significance":[],"seq_region_name":"7","id":"rs868464697","end":140605107,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140605107,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs893797868","end":140605110,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140605110,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140605112,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140605112,"source":"dbSNP","seq_region_name":"7","id":"rs1799644029","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605116,"feature_type":"variation","strand":1,"end":140605117,"alleles":["CC","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs749755163"},{"source":"dbSNP","start":140605117,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140605117,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1212776917","seq_region_name":"7"},{"start":140605118,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140605118,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs946513972","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605119,"feature_type":"variation","strand":1,"end":140605119,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1270322661"},{"alleles":["A","G"],"end":140605120,"feature_type":"variation","strand":1,"source":"dbSNP","start":140605120,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs546574684"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140605122,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140605122,"seq_region_name":"7","id":"rs1346993833","clinical_significance":[]},{"source":"dbSNP","start":140605126,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["CCTAC","CCTACCTAC"],"end":140605130,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799644821","seq_region_name":"7"},{"id":"rs977960206","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140605127,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140605127,"source":"dbSNP"},{"end":140605130,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140605130,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs924651407"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140605131,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605131,"clinical_significance":[],"seq_region_name":"7","id":"rs1799645193"},{"alleles":["A","C"],"end":140605132,"feature_type":"variation","strand":1,"source":"dbSNP","start":140605132,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs934743970"},{"seq_region_name":"7","id":"rs1057177512","clinical_significance":[],"alleles":["G","C"],"end":140605133,"strand":1,"feature_type":"variation","start":140605133,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["C","T"],"end":140605137,"strand":1,"feature_type":"variation","start":140605137,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1035166133","clinical_significance":[]},{"seq_region_name":"7","id":"rs1204095940","clinical_significance":[],"start":140605138,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140605138,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"start":140605151,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140605151,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799645811","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130693458","clinical_significance":[],"end":140605154,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140605154,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140605155,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140605155,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799645912"},{"alleles":["C","G"],"end":140605157,"feature_type":"variation","strand":1,"source":"dbSNP","start":140605157,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1253232189"},{"seq_region_name":"7","id":"rs1469535192","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140605160,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140605160,"source":"dbSNP"},{"id":"rs1799646266","seq_region_name":"7","clinical_significance":[],"alleles":["T","G"],"end":140605162,"strand":1,"feature_type":"variation","start":140605162,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799646369","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605163,"feature_type":"variation","strand":1,"end":140605163,"alleles":["G","T"]},{"seq_region_name":"7","id":"rs2130693488","clinical_significance":[],"start":140605170,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140605170,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140605176,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140605176,"source":"dbSNP","seq_region_name":"7","id":"rs1458162420","clinical_significance":[]},{"start":140605179,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140605179,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs1391252168","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140605181,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605181,"clinical_significance":[],"seq_region_name":"7","id":"rs369060330"},{"clinical_significance":[],"id":"rs959785434","seq_region_name":"7","source":"dbSNP","start":140605184,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140605184,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1013084221","seq_region_name":"7","alleles":["G","T"],"end":140605186,"feature_type":"variation","strand":1,"source":"dbSNP","start":140605186,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605187,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140605187,"clinical_significance":[],"seq_region_name":"7","id":"rs1362743619"},{"end":140605191,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140605191,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs895807778","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140605197,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140605197,"seq_region_name":"7","id":"rs1585741399","clinical_significance":[]},{"alleles":["C","T"],"end":140605210,"feature_type":"variation","strand":1,"source":"dbSNP","start":140605210,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs948746529"},{"seq_region_name":"7","id":"rs565055643","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140605211,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140605211,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140605217,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605217,"clinical_significance":[],"seq_region_name":"7","id":"rs1192928911"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799647610","end":140605226,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140605226,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140605229,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140605229,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799647687"},{"seq_region_name":"7","id":"rs1160427306","clinical_significance":[],"strand":1,"feature_type":"variation","end":140605230,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140605230,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs888716103","alleles":["C","G"],"end":140605231,"feature_type":"variation","strand":1,"source":"dbSNP","start":140605231,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1451709035","clinical_significance":[],"alleles":["T","C"],"end":140605232,"strand":1,"feature_type":"variation","start":140605232,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1799648146","seq_region_name":"7","feature_type":"variation","strand":1,"end":140605233,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605233},{"id":"rs532400318","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140605234,"strand":1,"feature_type":"variation","start":140605234,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140605236,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140605236,"id":"rs1320052917","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1203633165","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140605238,"source":"dbSNP","strand":1,"feature_type":"variation","end":140605238,"alleles":["G","A"]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140605244,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140605244,"source":"dbSNP","seq_region_name":"7","id":"rs1585741496","clinical_significance":[]},{"id":"rs1006097619","seq_region_name":"7","clinical_significance":[],"start":140605245,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140605245,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs919152509","end":140605250,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140605250,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs950624522","clinical_significance":[],"alleles":["C","T"],"end":140605251,"strand":1,"feature_type":"variation","start":140605251,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1799649050","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140605254,"source":"dbSNP","strand":1,"feature_type":"variation","end":140605254,"alleles":["C","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605255,"feature_type":"variation","strand":1,"end":140605255,"alleles":["T","A"],"clinical_significance":[],"id":"rs1015763945","seq_region_name":"7"},{"alleles":["C","T"],"end":140605256,"feature_type":"variation","strand":1,"source":"dbSNP","start":140605256,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1303371585"},{"start":140605258,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140605258,"alleles":["G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799649356","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140605260,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605260,"clinical_significance":[],"id":"rs1436435437","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140605268,"source":"dbSNP","strand":1,"feature_type":"variation","end":140605268,"alleles":["A","G"],"seq_region_name":"7","id":"rs987268647","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs550584070","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605269,"feature_type":"variation","strand":1,"end":140605269,"alleles":["C","G"]},{"seq_region_name":"7","id":"rs1380176907","clinical_significance":[],"start":140605270,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140605270,"strand":1,"feature_type":"variation"},{"start":140605274,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140605274,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799649868","clinical_significance":[]},{"alleles":["T","C"],"end":140605277,"strand":1,"feature_type":"variation","start":140605277,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799649963","clinical_significance":[]},{"seq_region_name":"7","id":"rs997923951","clinical_significance":[],"alleles":["G","A"],"end":140605279,"strand":1,"feature_type":"variation","start":140605279,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140605287,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140605287,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130693676"},{"alleles":["G","A"],"end":140605289,"strand":1,"feature_type":"variation","start":140605289,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799650151","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs943256879","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605291,"feature_type":"variation","strand":1,"end":140605291,"alleles":["A","G"]},{"start":140605295,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140605295,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1297334580","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140605297,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140605297,"source":"dbSNP","id":"rs78700417","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799650540","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140605304,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140605304,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799650652","end":140605307,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140605307,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["T","C"],"end":140605309,"strand":1,"feature_type":"variation","start":140605309,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1436116319","clinical_significance":[]},{"end":140605310,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140605310,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799650844","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140605313,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605313,"clinical_significance":[],"seq_region_name":"7","id":"rs953671942"},{"clinical_significance":[],"id":"rs1799651042","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140605314,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605314},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799651138","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605321,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140605321},{"seq_region_name":"7","id":"rs1799651241","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140605328,"source":"dbSNP","strand":1,"feature_type":"variation","end":140605328,"alleles":["T","A"]},{"end":140605331,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140605331,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs915358356","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140605332,"source":"dbSNP","strand":1,"feature_type":"variation","end":140605332,"alleles":["G","A"],"seq_region_name":"7","id":"rs1309037551","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1172983731","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605333,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140605333},{"clinical_significance":[],"seq_region_name":"7","id":"rs536034870","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140605337,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605337},{"end":140605338,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140605338,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1449948563","clinical_significance":[]},{"id":"rs1799651861","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140605340,"strand":1,"feature_type":"variation","start":140605340,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140605341,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140605341,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799651963"},{"alleles":["G","C"],"end":140605342,"feature_type":"variation","strand":1,"source":"dbSNP","start":140605342,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs774751591"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1315123698","source":"dbSNP","start":140605345,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140605345,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140605347,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140605347,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1374613675"},{"id":"rs1799652373","seq_region_name":"7","clinical_significance":[],"start":140605349,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140605349,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140605351,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["ACTGACTG","ACTG"],"end":140605358,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs946701230"},{"alleles":["C","G"],"end":140605352,"strand":1,"feature_type":"variation","start":140605352,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799652560","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799652669","clinical_significance":[],"alleles":["G","C"],"end":140605354,"strand":1,"feature_type":"variation","start":140605354,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs985159390","seq_region_name":"7","source":"dbSNP","start":140605356,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140605356,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605357,"feature_type":"variation","strand":1,"end":140605361,"alleles":["TGTGT","TGTGTGT"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585741721"},{"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140605359,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605359,"clinical_significance":[],"seq_region_name":"7","id":"rs1042391286"},{"clinical_significance":[],"id":"rs902746188","seq_region_name":"7","source":"dbSNP","start":140605361,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140605361,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1799653219","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140605362,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140605362},{"end":140605363,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140605363,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs759727752","clinical_significance":[]},{"start":140605372,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140605372,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs1799653413","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799653502","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140605373,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140605373,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140605383,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605383,"clinical_significance":[],"id":"rs1799653656","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs548313729","alleles":["G","C"],"end":140605387,"feature_type":"variation","strand":1,"source":"dbSNP","start":140605387,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","T"],"end":140605388,"strand":1,"feature_type":"variation","start":140605388,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1003760438","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605392,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140605392,"clinical_significance":[],"seq_region_name":"7","id":"rs1022598277"},{"clinical_significance":[],"id":"rs554208808","seq_region_name":"7","alleles":["A","G"],"end":140605395,"feature_type":"variation","strand":1,"source":"dbSNP","start":140605395,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140605397,"source":"dbSNP","strand":1,"feature_type":"variation","end":140605397,"alleles":["A","C"],"id":"rs566583303","seq_region_name":"7","clinical_significance":[]},{"id":"rs557440193","seq_region_name":"7","clinical_significance":[],"alleles":["AA","A"],"end":140605398,"strand":1,"feature_type":"variation","start":140605397,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1012444203","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140605398,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140605398,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605399,"feature_type":"variation","strand":1,"end":140605399,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1563173843"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1211473268","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140605415,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605415},{"seq_region_name":"7","id":"rs1252031346","clinical_significance":[],"end":140605422,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","start":140605422,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1488345846","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140605424,"source":"dbSNP","strand":1,"feature_type":"variation","end":140605424,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1799655035","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140605428,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140605428,"source":"dbSNP"},{"clinical_significance":[],"id":"rs2130693941","seq_region_name":"7","end":140605434,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140605434,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140605438,"source":"dbSNP","strand":1,"feature_type":"variation","end":140605438,"alleles":["C","A","T"],"seq_region_name":"7","id":"rs1227228966","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140605444,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140605444,"source":"dbSNP","seq_region_name":"7","id":"rs1334447769","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605452,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140605452,"clinical_significance":[],"id":"rs13239367","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs939215726","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605453,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140605453},{"start":140605454,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140605454,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs13220994","clinical_significance":[]},{"clinical_significance":[],"id":"rs992854334","seq_region_name":"7","end":140605455,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140605455,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605457,"feature_type":"variation","strand":1,"end":140605457,"alleles":["T","C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs917350144"},{"end":140605461,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140605461,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799655984"},{"end":140605463,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140605463,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs13220998","clinical_significance":[]},{"start":140605465,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140605465,"alleles":["G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs13228625","clinical_significance":[]},{"id":"rs7789086","seq_region_name":"7","clinical_significance":[],"start":140605467,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140605467,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs2130694011","clinical_significance":[],"start":140605472,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140605472,"strand":1,"feature_type":"variation"},{"alleles":["G","T"],"end":140605473,"strand":1,"feature_type":"variation","start":140605473,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1166086430","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs577155839","alleles":["T","C"],"end":140605474,"feature_type":"variation","strand":1,"source":"dbSNP","start":140605474,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140605481,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140605481,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799656570"},{"end":140605483,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140605483,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130694034","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799656686","clinical_significance":[],"end":140605486,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140605486,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1044408201","feature_type":"variation","strand":1,"alleles":["T","A"],"end":140605488,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605488},{"source":"dbSNP","start":140605490,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140605490,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799656871"},{"id":"rs1799656963","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140605494,"source":"dbSNP","strand":1,"feature_type":"variation","end":140605494,"alleles":["C","T"]},{"source":"dbSNP","start":140605502,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C","G"],"end":140605502,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585741960"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140605506,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140605506,"seq_region_name":"7","id":"rs1799657124","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1474985518","alleles":["A","G"],"end":140605510,"feature_type":"variation","strand":1,"source":"dbSNP","start":140605510,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140605514,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140605514,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1463177865"},{"alleles":["G","C"],"end":140605515,"strand":1,"feature_type":"variation","start":140605515,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs888654486","clinical_significance":[]},{"clinical_significance":[],"id":"rs1349569702","seq_region_name":"7","source":"dbSNP","start":140605517,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140605517,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs201579962","clinical_significance":[],"start":140605517,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140605523,"alleles":["CTCTCTC","CTCTC","CTCTCTCTC"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1491045876","clinical_significance":[],"end":140605517,"alleles":["-","CT"],"strand":1,"feature_type":"variation","start":140605518,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140605521,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605521,"clinical_significance":[],"seq_region_name":"7","id":"rs1799657818"},{"clinical_significance":[],"seq_region_name":"7","id":"rs113372848","feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140605523,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605523},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605524,"feature_type":"variation","strand":1,"end":140605523,"alleles":["-","TT"],"clinical_significance":[],"seq_region_name":"7","id":"rs113822626"},{"id":"rs1299671089","seq_region_name":"7","clinical_significance":[],"end":140605524,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140605524,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1378772623","clinical_significance":[],"end":140605524,"alleles":["-","TT"],"strand":1,"feature_type":"variation","start":140605525,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1371012651","seq_region_name":"7","source":"dbSNP","start":140605527,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","G"],"end":140605527,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140605535,"source":"dbSNP","strand":1,"feature_type":"variation","end":140605535,"alleles":["C","T"],"seq_region_name":"7","id":"rs538560196","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1439617374","source":"dbSNP","start":140605544,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140605544,"alleles":["T","A"],"feature_type":"variation","strand":1},{"alleles":["T","A","C"],"end":140605549,"strand":1,"feature_type":"variation","start":140605549,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1037720399","clinical_significance":[]},{"id":"rs1357548347","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140605551,"source":"dbSNP","strand":1,"feature_type":"variation","end":140605551,"alleles":["A","G"]},{"id":"rs1799658900","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140605552,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140605552},{"clinical_significance":[],"id":"rs1585742095","seq_region_name":"7","feature_type":"variation","strand":1,"end":140605553,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605553},{"start":140605556,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140605556,"alleles":["A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799659111","clinical_significance":[]},{"alleles":["T","C"],"end":140605558,"strand":1,"feature_type":"variation","start":140605558,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs556579882","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799659299","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605560,"feature_type":"variation","strand":1,"end":140605560,"alleles":["C","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130694169","end":140605567,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140605567,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799659394","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140605568,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605568},{"alleles":["G","A","T"],"end":140605569,"strand":1,"feature_type":"variation","start":140605569,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1234779077","clinical_significance":[]},{"end":140605571,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140605571,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs950573380","clinical_significance":[]},{"alleles":["T","G"],"end":140605573,"feature_type":"variation","strand":1,"source":"dbSNP","start":140605573,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799659727"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605575,"feature_type":"variation","strand":1,"end":140605575,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs756181435"},{"alleles":["A","C"],"end":140605576,"strand":1,"feature_type":"variation","start":140605576,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1029391465","clinical_significance":[]},{"seq_region_name":"7","id":"rs764087205","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140605581,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140605581,"source":"dbSNP"},{"end":140605585,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140605585,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1355746362","clinical_significance":[]},{"source":"dbSNP","start":140605587,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140605587,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130694219"},{"seq_region_name":"7","id":"rs750318207","clinical_significance":[],"end":140605592,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140605592,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1799660324","seq_region_name":"7","clinical_significance":[],"end":140605594,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140605594,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["C","T"],"end":140605595,"strand":1,"feature_type":"variation","start":140605595,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs758326961","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799660539","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605602,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140605602},{"seq_region_name":"7","id":"rs1799660646","clinical_significance":[],"start":140605611,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140605611,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1409252538","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140605612,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140605612},{"start":140605615,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140605615,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1391229212","clinical_significance":[]},{"alleles":["T","G"],"end":140605616,"strand":1,"feature_type":"variation","start":140605616,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs964889287","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605619,"feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140605619,"clinical_significance":[],"id":"rs968153784","seq_region_name":"7"},{"seq_region_name":"7","id":"rs779990622","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140605623,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140605623},{"feature_type":"variation","strand":1,"end":140605625,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605625,"clinical_significance":[],"id":"rs1799661269","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs189393042","alleles":["G","C"],"end":140605628,"feature_type":"variation","strand":1,"source":"dbSNP","start":140605628,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1417481713","feature_type":"variation","strand":1,"end":140605641,"alleles":["GAAGAAG","GAAG"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605635},{"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140605656,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605656,"clinical_significance":[],"seq_region_name":"7","id":"rs1183155340"},{"seq_region_name":"7","id":"rs558328425","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140605661,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140605661,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140605663,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140605663,"source":"dbSNP","seq_region_name":"7","id":"rs1799661830","clinical_significance":[]},{"seq_region_name":"7","id":"rs915288569","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140605665,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140605665,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140605672,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605672,"clinical_significance":[],"id":"rs137916753","seq_region_name":"7"},{"source":"dbSNP","start":140605673,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140605673,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs978031273"},{"seq_region_name":"7","id":"rs73736639","clinical_significance":[],"start":140605674,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140605674,"alleles":["G","A","C"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605676,"feature_type":"variation","strand":1,"end":140605686,"alleles":["CTACACTCTCG","CTACACTCTCGCTACACTCTCG"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799662413"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140605679,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140605679,"source":"dbSNP","id":"rs1272200863","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799662520","alleles":["A","G"],"end":140605680,"feature_type":"variation","strand":1,"source":"dbSNP","start":140605680,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140605681,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605681,"clinical_significance":[],"seq_region_name":"7","id":"rs991966199"},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140605683,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605683,"clinical_significance":[],"id":"rs1799662764","seq_region_name":"7"},{"start":140605685,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140605685,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs917294813","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605686,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140605686,"clinical_significance":[],"seq_region_name":"7","id":"rs970168124"},{"seq_region_name":"7","id":"rs1799663115","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140605692,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140605692,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140605693,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605693,"clinical_significance":[],"seq_region_name":"7","id":"rs754653648"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605696,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140605696,"clinical_significance":[],"seq_region_name":"7","id":"rs1799663317"},{"assembly_name":"GRCh38","consequence_type":"splice_region_variant","start":140605697,"source":"dbSNP","strand":1,"feature_type":"variation","end":140605697,"alleles":["G","A"],"id":"rs1413256883","seq_region_name":"7","clinical_significance":[]},{"start":140605700,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_donor_variant","end":140605706,"alleles":["CTTACTT","CTT"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799663549","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1410755331","end":140605703,"alleles":["A","AA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140605703,"consequence_type":"splice_donor_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585742364","consequence_type":"splice_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605705,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140605705},{"id":"rs1799663847","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"splice_region_variant","start":140605707,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140605707},{"seq_region_name":"7","id":"rs1172200311","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","start":140605709,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140605709},{"end":140605713,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140605713,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","seq_region_name":"7","id":"rs895421399","clinical_significance":[]},{"id":"rs948194086","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","start":140605715,"source":"dbSNP","strand":1,"feature_type":"variation","end":140605715,"alleles":["A","G"]},{"id":"rs1160245231","seq_region_name":"7","clinical_significance":[],"start":140605719,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","end":140605719,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1038548595","clinical_significance":[],"end":140605720,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140605720,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant"},{"source":"dbSNP","start":140605721,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140605721,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1405919560"},{"source":"dbSNP","start":140605722,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","end":140605722,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799664560","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140605723,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","start":140605723,"source":"dbSNP","seq_region_name":"7","id":"rs192395859","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","start":140605728,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140605728,"seq_region_name":"7","id":"rs1799664751","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1313385396","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140605733,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605733},{"end":140605735,"alleles":["AG","AGAG"],"strand":1,"feature_type":"variation","start":140605734,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","seq_region_name":"7","id":"rs1478649445","clinical_significance":[]},{"seq_region_name":"7","id":"rs1255521851","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","start":140605736,"source":"dbSNP","strand":1,"feature_type":"variation","end":140605736,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1799665138","clinical_significance":[],"start":140605740,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","end":140605740,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1357351490","alleles":["G","A","T"],"end":140605746,"feature_type":"variation","strand":1,"source":"dbSNP","start":140605746,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1799665382","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","start":140605748,"source":"dbSNP","strand":1,"feature_type":"variation","end":140605748,"alleles":["T","C"]},{"id":"rs1799665480","seq_region_name":"7","clinical_significance":[],"start":140605750,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","alleles":["C","T"],"end":140605750,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1563174098","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140605751,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605751},{"seq_region_name":"7","id":"rs2130694489","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","start":140605753,"source":"dbSNP","strand":1,"feature_type":"variation","end":140605753,"alleles":["T","G"]},{"start":140605755,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","alleles":["G","A"],"end":140605755,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1468360321","clinical_significance":[]},{"id":"rs1799665806","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140605757,"alleles":["-","T"],"assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","start":140605758,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs6971171","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140605758,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605758},{"clinical_significance":[],"seq_region_name":"7","id":"rs994590419","consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605759,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140605759},{"alleles":["G","A"],"end":140605764,"strand":1,"feature_type":"variation","start":140605764,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","seq_region_name":"7","id":"rs1318279437","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799666272","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","start":140605765,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140605765},{"end":140605765,"alleles":["-","CACTG"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140605766,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799666382","seq_region_name":"7"},{"end":140605771,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140605771,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799666479","seq_region_name":"7"},{"id":"rs1222768088","seq_region_name":"7","clinical_significance":[],"end":140605772,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140605772,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant"},{"clinical_significance":[],"id":"rs377543652","seq_region_name":"7","source":"dbSNP","start":140605772,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","alleles":["TCATCAT","TCATCATCAT"],"end":140605778,"feature_type":"variation","strand":1},{"id":"rs1799666803","seq_region_name":"7","clinical_significance":[],"end":140605774,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140605774,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130694561","source":"dbSNP","start":140605776,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","end":140605776,"alleles":["C","T"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","start":140605777,"source":"dbSNP","strand":1,"feature_type":"variation","end":140605777,"alleles":["A","T"],"seq_region_name":"7","id":"rs1799666914","clinical_significance":[]},{"start":140605779,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","alleles":["G","GG"],"end":140605779,"strand":1,"feature_type":"variation","id":"rs1799667007","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799667109","seq_region_name":"7","source":"dbSNP","start":140605784,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140605784,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140605787,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605787,"clinical_significance":[],"seq_region_name":"7","id":"rs1799667216"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1215985876","source":"dbSNP","start":140605788,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140605788,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1305586906","seq_region_name":"7","end":140605789,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140605789,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140605794,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","start":140605794,"source":"dbSNP","seq_region_name":"7","id":"rs886099386","clinical_significance":[]},{"clinical_significance":[],"id":"rs1370007079","seq_region_name":"7","end":140605798,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140605798,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799667694","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140605799,"consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605799},{"clinical_significance":[],"id":"rs1799667795","seq_region_name":"7","consequence_type":"5_prime_UTR_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605801,"feature_type":"variation","strand":1,"end":140605801,"alleles":["G","C"]},{"seq_region_name":"7","id":"rs1585742570","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140605803,"assembly_name":"GRCh38","consequence_type":"5_prime_UTR_variant","start":140605803,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1585742581","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140605808,"assembly_name":"GRCh38","consequence_type":"splice_acceptor_variant","start":140605808,"source":"dbSNP"},{"source":"dbSNP","start":140605809,"consequence_type":"splice_region_variant","assembly_name":"GRCh38","end":140605809,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799668082"},{"consequence_type":"splice_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605810,"feature_type":"variation","strand":1,"end":140605810,"alleles":["G","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585742589"},{"seq_region_name":"7","id":"rs1008593688","clinical_significance":[],"alleles":["G","A","C"],"end":140605811,"strand":1,"feature_type":"variation","start":140605811,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"splice_region_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799668429","consequence_type":"splice_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605812,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140605812},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140605813,"assembly_name":"GRCh38","consequence_type":"splice_region_variant","start":140605813,"source":"dbSNP","seq_region_name":"7","id":"rs1799668538","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A","C","T"],"end":140605814,"consequence_type":"splice_region_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605814,"clinical_significance":[],"seq_region_name":"7","id":"rs1340444747"},{"seq_region_name":"7","id":"rs1799668782","clinical_significance":[],"start":140605825,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140605825,"strand":1,"feature_type":"variation"},{"id":"rs1799668891","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140605826,"source":"dbSNP","strand":1,"feature_type":"variation","end":140605826,"alleles":["C","T"]},{"start":140605829,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140605829,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799669000","clinical_significance":[]},{"end":140605831,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140605831,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799669100","clinical_significance":[]},{"end":140605835,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140605835,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799669212","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140605837,"source":"dbSNP","strand":1,"feature_type":"variation","end":140605837,"alleles":["C","A","T"],"seq_region_name":"7","id":"rs1433155982","clinical_significance":[]},{"alleles":["A","G"],"end":140605839,"feature_type":"variation","strand":1,"source":"dbSNP","start":140605839,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585742615"},{"seq_region_name":"7","id":"rs1563174162","clinical_significance":[],"start":140605850,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140605850,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1204958217","feature_type":"variation","strand":1,"end":140605851,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605851},{"alleles":["G","A"],"end":140605860,"strand":1,"feature_type":"variation","start":140605860,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585742648","clinical_significance":[]},{"start":140605864,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140605864,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1281654840","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605866,"feature_type":"variation","strand":1,"end":140605866,"alleles":["A","G"],"clinical_significance":[],"id":"rs941383940","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1563174180","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140605867,"source":"dbSNP","strand":1,"feature_type":"variation","end":140605867,"alleles":["G","A"]},{"start":140605870,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140605870,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1343593912","clinical_significance":[]},{"seq_region_name":"7","id":"rs780941467","clinical_significance":[],"strand":1,"feature_type":"variation","end":140605872,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140605872,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1486941281","clinical_significance":[],"end":140605873,"alleles":["C","A","G"],"strand":1,"feature_type":"variation","start":140605873,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140605877,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140605877,"source":"dbSNP","seq_region_name":"7","id":"rs1799670492","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799670597","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140605879,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605879},{"seq_region_name":"7","id":"rs1799670692","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140605880,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140605880},{"alleles":["C","T"],"end":140605881,"strand":1,"feature_type":"variation","start":140605881,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1317888322","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140605883,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140605883,"source":"dbSNP","seq_region_name":"7","id":"rs1799670901","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140605887,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605887,"clinical_significance":[],"seq_region_name":"7","id":"rs1799671011"},{"strand":1,"feature_type":"variation","end":140605888,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140605888,"source":"dbSNP","seq_region_name":"7","id":"rs1415152702","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799671201","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605892,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140605892},{"start":140605893,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140605893,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799671291","clinical_significance":[]},{"id":"rs1799671395","seq_region_name":"7","clinical_significance":[],"end":140605894,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140605894,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130694787","end":140605900,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140605900,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1037263864","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140605901,"source":"dbSNP","strand":1,"feature_type":"variation","end":140605901,"alleles":["C","A","G","T"]},{"feature_type":"variation","strand":1,"end":140605913,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605913,"clinical_significance":[],"seq_region_name":"7","id":"rs1396947648"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1208037225","source":"dbSNP","start":140605915,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140605915,"feature_type":"variation","strand":1},{"alleles":["C","A"],"end":140605916,"feature_type":"variation","strand":1,"source":"dbSNP","start":140605916,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1236995393"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799671964","feature_type":"variation","strand":1,"end":140605923,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605923},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605924,"feature_type":"variation","strand":1,"alleles":["A","-"],"end":140605924,"clinical_significance":[],"seq_region_name":"7","id":"rs1475839679"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1188599564","end":140605925,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140605925,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140605926,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140605926,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1485091636"},{"clinical_significance":[],"id":"rs747784380","seq_region_name":"7","source":"dbSNP","start":140605927,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140605927,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140605929,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605929,"clinical_significance":[],"seq_region_name":"7","id":"rs1019260607"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605939,"feature_type":"variation","strand":1,"end":140605939,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1485738977"},{"alleles":["A","G"],"end":140605940,"feature_type":"variation","strand":1,"source":"dbSNP","start":140605940,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799672664"},{"strand":1,"feature_type":"variation","end":140605941,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140605941,"source":"dbSNP","seq_region_name":"7","id":"rs577109141","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799672899","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140605942,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140605942,"source":"dbSNP"},{"source":"dbSNP","start":140605943,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140605943,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs550899277"},{"alleles":["A","G"],"end":140605944,"feature_type":"variation","strand":1,"source":"dbSNP","start":140605944,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1232024583"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799673118","source":"dbSNP","start":140605956,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140605956,"feature_type":"variation","strand":1},{"end":140605960,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140605960,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1417698625"},{"seq_region_name":"7","id":"rs2130694907","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140605967,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140605967,"source":"dbSNP"},{"source":"dbSNP","start":140605974,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140605974,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs2130694914","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1799673336","seq_region_name":"7","alleles":["G","A"],"end":140605975,"feature_type":"variation","strand":1,"source":"dbSNP","start":140605975,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1292629246","feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140605976,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605976},{"clinical_significance":[],"seq_region_name":"7","id":"rs1051270637","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605982,"feature_type":"variation","strand":1,"end":140605982,"alleles":["C","G"]},{"id":"rs889999922","seq_region_name":"7","clinical_significance":[],"start":140605986,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140605986,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1006634696","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140605988,"source":"dbSNP","strand":1,"feature_type":"variation","end":140605988,"alleles":["C","G","T"]},{"clinical_significance":[],"id":"rs540929805","seq_region_name":"7","source":"dbSNP","start":140605989,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140605989,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140605991,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140605991,"id":"rs2130694961","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140605992,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140605992,"source":"dbSNP","seq_region_name":"7","id":"rs1799673920","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs903499027","feature_type":"variation","strand":1,"end":140605995,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140605995},{"clinical_significance":[],"seq_region_name":"7","id":"rs1415574888","alleles":["G","A"],"end":140605996,"feature_type":"variation","strand":1,"source":"dbSNP","start":140605996,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140605999,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140605999,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs999615150","clinical_significance":[]},{"alleles":["G","A"],"end":140606000,"strand":1,"feature_type":"variation","start":140606000,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs76125842","clinical_significance":[]},{"alleles":["A","G"],"end":140606006,"feature_type":"variation","strand":1,"source":"dbSNP","start":140606006,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs924055003"},{"seq_region_name":"7","id":"rs1799674573","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140606007,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606007,"source":"dbSNP"},{"end":140606014,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140606014,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799674656"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606017,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140606017,"clinical_significance":[],"seq_region_name":"7","id":"rs1799674744"},{"start":140606021,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140606021,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs529846534","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140606022,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606022,"source":"dbSNP","id":"rs960620022","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs992188593","end":140606025,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140606025,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140606028,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606028,"clinical_significance":[],"seq_region_name":"7","id":"rs1799674940"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140606029,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606029,"source":"dbSNP","seq_region_name":"7","id":"rs779069600","clinical_significance":[]},{"source":"dbSNP","start":140606031,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140606031,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799675177"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606032,"source":"dbSNP","strand":1,"feature_type":"variation","end":140606032,"alleles":["T","C"],"seq_region_name":"7","id":"rs1023421549","clinical_significance":[]},{"alleles":["T","C"],"end":140606034,"strand":1,"feature_type":"variation","start":140606034,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1799675370","seq_region_name":"7","clinical_significance":[]},{"start":140606035,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140606035,"alleles":["C","A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs948338030","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606036,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140606036,"clinical_significance":[],"id":"rs1799675624","seq_region_name":"7"},{"start":140606037,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140606037,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799675719","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1185591695","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606038,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140606038},{"clinical_significance":[],"seq_region_name":"7","id":"rs1475305625","source":"dbSNP","start":140606040,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140606040,"alleles":["T","C"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606045,"source":"dbSNP","strand":1,"feature_type":"variation","end":140606045,"alleles":["C","T"],"seq_region_name":"7","id":"rs79373975","clinical_significance":[]},{"seq_region_name":"7","id":"rs75560897","clinical_significance":[],"end":140606046,"alleles":["A","C","G","T"],"strand":1,"feature_type":"variation","start":140606046,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs75557499","end":140606047,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140606047,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1259011470","seq_region_name":"7","source":"dbSNP","start":140606048,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140606048,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs114685763","clinical_significance":[],"strand":1,"feature_type":"variation","end":140606050,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606050,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["G","-"],"end":140606050,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606050,"clinical_significance":[],"seq_region_name":"7","id":"rs898661273"},{"strand":1,"feature_type":"variation","end":140606051,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606051,"source":"dbSNP","id":"rs1286737054","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140606051,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140606058,"alleles":["TTTTTTTT","TTTTTTT","TTTTTTTTT"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs886213975"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1305574901","feature_type":"variation","strand":1,"end":140606052,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606052},{"seq_region_name":"7","id":"rs1799677228","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140606058,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606058,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1271974373","clinical_significance":[],"strand":1,"feature_type":"variation","end":140606065,"alleles":["AG","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606064,"source":"dbSNP"},{"source":"dbSNP","start":140606065,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140606065,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1364088978"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606066,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140606066,"clinical_significance":[],"seq_region_name":"7","id":"rs1799677555"},{"clinical_significance":[],"id":"rs1799677651","seq_region_name":"7","source":"dbSNP","start":140606067,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140606067,"alleles":["G","A","T"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140606077,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606077,"source":"dbSNP","seq_region_name":"7","id":"rs1799677774","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130695158","clinical_significance":[],"strand":1,"feature_type":"variation","end":140606082,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606082,"source":"dbSNP"},{"end":140606090,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140606090,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1234134703","clinical_significance":[]},{"clinical_significance":[],"id":"rs1563174396","seq_region_name":"7","source":"dbSNP","start":140606093,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140606093,"alleles":["T","C"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140606100,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606100,"clinical_significance":[],"id":"rs1357550357","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140606101,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606101,"source":"dbSNP","seq_region_name":"7","id":"rs1228035668","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606103,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140606103,"clinical_significance":[],"seq_region_name":"7","id":"rs1304640666"},{"alleles":["C","T"],"end":140606105,"strand":1,"feature_type":"variation","start":140606105,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799678401","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606110,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140606110,"clinical_significance":[],"seq_region_name":"7","id":"rs1799678496"},{"id":"rs980193896","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606113,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140606113},{"strand":1,"feature_type":"variation","end":140606116,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606116,"source":"dbSNP","seq_region_name":"7","id":"rs909976105","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1374111616","source":"dbSNP","start":140606117,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140606117,"alleles":["C","T"],"feature_type":"variation","strand":1},{"alleles":["G","A"],"end":140606118,"feature_type":"variation","strand":1,"source":"dbSNP","start":140606118,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs748513949"},{"strand":1,"feature_type":"variation","end":140606122,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606122,"source":"dbSNP","id":"rs1799678996","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs759848533","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140606125,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606125},{"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140606126,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606126,"source":"dbSNP","seq_region_name":"7","id":"rs972737122","clinical_significance":[]},{"seq_region_name":"7","id":"rs566644303","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140606127,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606127,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606128,"feature_type":"variation","strand":1,"end":140606129,"alleles":["CC","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1166017531"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606130,"source":"dbSNP","strand":1,"feature_type":"variation","end":140606130,"alleles":["T","G"],"seq_region_name":"7","id":"rs1018625775","clinical_significance":[]},{"seq_region_name":"7","id":"rs1419651443","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140606135,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606135,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799679737","clinical_significance":[],"alleles":["C","A","T"],"end":140606137,"strand":1,"feature_type":"variation","start":140606137,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140606140,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","start":140606140,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs918806170","seq_region_name":"7","clinical_significance":[]},{"start":140606140,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140606141,"alleles":["AA","A"],"strand":1,"feature_type":"variation","id":"rs1218008460","seq_region_name":"7","clinical_significance":[]},{"end":140606145,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140606145,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs533993766"},{"end":140606147,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140606147,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1799680102","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1250559359","end":140606150,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140606150,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140606151,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140606151,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1278585822"},{"source":"dbSNP","start":140606152,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140606152,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs774908908"},{"clinical_significance":[],"id":"rs2130695326","seq_region_name":"7","alleles":["C","T"],"end":140606155,"feature_type":"variation","strand":1,"source":"dbSNP","start":140606155,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606159,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140606159,"id":"rs1799680562","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs552371316","seq_region_name":"7","alleles":["C","T"],"end":140606160,"feature_type":"variation","strand":1,"source":"dbSNP","start":140606160,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799680797","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606165,"feature_type":"variation","strand":1,"end":140606165,"alleles":["C","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606166,"source":"dbSNP","strand":1,"feature_type":"variation","end":140606166,"alleles":["C","G","T"],"seq_region_name":"7","id":"rs1336673035","clinical_significance":[]},{"alleles":["G","A"],"end":140606168,"strand":1,"feature_type":"variation","start":140606168,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs911382350","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606170,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140606170,"clinical_significance":[],"seq_region_name":"7","id":"rs1799681086"},{"alleles":["G","A"],"end":140606176,"strand":1,"feature_type":"variation","start":140606176,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1271553824","clinical_significance":[]},{"source":"dbSNP","start":140606178,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140606178,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799681285"},{"id":"rs1022209695","seq_region_name":"7","clinical_significance":[],"end":140606181,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140606181,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585743328","alleles":["G","A"],"end":140606184,"feature_type":"variation","strand":1,"source":"dbSNP","start":140606184,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs269245","end":140606186,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140606186,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140606188,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140606188,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1464618800","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1799681743","seq_region_name":"7","feature_type":"variation","strand":1,"end":140606194,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606194},{"clinical_significance":[],"seq_region_name":"7","id":"rs1043458061","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606195,"feature_type":"variation","strand":1,"end":140606195,"alleles":["C","T"]},{"strand":1,"feature_type":"variation","end":140606196,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606196,"source":"dbSNP","seq_region_name":"7","id":"rs1193968538","clinical_significance":[]},{"source":"dbSNP","start":140606197,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140606197,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1396685427"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1327148371","feature_type":"variation","strand":1,"end":140606198,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606198},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606200,"source":"dbSNP","strand":1,"feature_type":"variation","end":140606200,"alleles":["C","T"],"seq_region_name":"7","id":"rs537844767","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606201,"feature_type":"variation","strand":1,"alleles":["-","T"],"end":140606200,"clinical_significance":[],"seq_region_name":"7","id":"rs113686349"},{"end":140606201,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140606201,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1031020322","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606202,"source":"dbSNP","strand":1,"feature_type":"variation","end":140606202,"alleles":["G","A"],"seq_region_name":"7","id":"rs1799682611","clinical_significance":[]},{"seq_region_name":"7","id":"rs556825922","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606203,"source":"dbSNP","strand":1,"feature_type":"variation","end":140606203,"alleles":["C","T"]},{"clinical_significance":[],"id":"rs1799682715","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606204,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140606204},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606212,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140606212,"id":"rs1799682798","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140606217,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606217,"clinical_significance":[],"seq_region_name":"7","id":"rs1408696826"},{"alleles":["T","C"],"end":140606219,"strand":1,"feature_type":"variation","start":140606219,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs760822061","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606221,"source":"dbSNP","strand":1,"feature_type":"variation","end":140606221,"alleles":["G","A","T"],"id":"rs896195415","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799683192","clinical_significance":[],"end":140606223,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140606223,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140606227,"alleles":["A","AA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606227,"clinical_significance":[],"seq_region_name":"7","id":"rs1401927726"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1013446970","alleles":["C","A","T"],"end":140606228,"feature_type":"variation","strand":1,"source":"dbSNP","start":140606228,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1023535917","seq_region_name":"7","clinical_significance":[],"end":140606229,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140606229,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1469691017","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606233,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140606233},{"id":"rs1441205412","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606238,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140606238},{"seq_region_name":"7","id":"rs905002895","clinical_significance":[],"alleles":["G","A"],"end":140606242,"strand":1,"feature_type":"variation","start":140606242,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140606247,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140606247,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1213334032"},{"seq_region_name":"7","id":"rs1799683946","clinical_significance":[],"alleles":["A","G"],"end":140606249,"strand":1,"feature_type":"variation","start":140606249,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["G","C"],"end":140606250,"strand":1,"feature_type":"variation","start":140606250,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799684041","clinical_significance":[]},{"source":"dbSNP","start":140606256,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140606256,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1585743488","seq_region_name":"7"},{"end":140606265,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140606265,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799684226","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs960833052","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140606269,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606269},{"seq_region_name":"7","id":"rs1585743498","clinical_significance":[],"start":140606273,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140606273,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140606278,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140606278,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs992531977"},{"seq_region_name":"7","id":"rs1799684622","clinical_significance":[],"end":140606281,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140606281,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs568723981","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140606282,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606282,"source":"dbSNP"},{"start":140606283,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140606283,"alleles":["G","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130695546","clinical_significance":[]},{"alleles":["C","T"],"end":140606289,"strand":1,"feature_type":"variation","start":140606289,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1237047597","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1316408800","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140606293,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606293},{"seq_region_name":"7","id":"rs536078489","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606294,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140606294},{"id":"rs1434822759","seq_region_name":"7","clinical_significance":[],"start":140606295,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140606295,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140606298,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606298,"clinical_significance":[],"seq_region_name":"7","id":"rs1237083943"},{"id":"rs1799685262","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606299,"source":"dbSNP","strand":1,"feature_type":"variation","end":140606299,"alleles":["C","G"]},{"alleles":["G","T"],"end":140606303,"feature_type":"variation","strand":1,"source":"dbSNP","start":140606303,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1274763314"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606308,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140606308,"seq_region_name":"7","id":"rs1799685467","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1325572588","feature_type":"variation","strand":1,"end":140606309,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606309},{"seq_region_name":"7","id":"rs1799685653","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140606314,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606314,"source":"dbSNP"},{"clinical_significance":[],"id":"rs778398262","seq_region_name":"7","alleles":["C","A","T"],"end":140606316,"feature_type":"variation","strand":1,"source":"dbSNP","start":140606316,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140606317,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606317,"source":"dbSNP","seq_region_name":"7","id":"rs145999884","clinical_significance":[]},{"alleles":["A","G"],"end":140606319,"feature_type":"variation","strand":1,"source":"dbSNP","start":140606319,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1266331306"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606322,"source":"dbSNP","strand":1,"feature_type":"variation","end":140606322,"alleles":["G","A"],"seq_region_name":"7","id":"rs1563174556","clinical_significance":[]},{"alleles":["A","C"],"end":140606323,"strand":1,"feature_type":"variation","start":140606323,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1799686216","seq_region_name":"7","clinical_significance":[]},{"end":140606324,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140606324,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs963121375","clinical_significance":[]},{"alleles":["G","A"],"end":140606337,"strand":1,"feature_type":"variation","start":140606337,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1451049051","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs972854333","source":"dbSNP","start":140606338,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140606338,"alleles":["C","G","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1379131647","seq_region_name":"7","source":"dbSNP","start":140606340,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140606340,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1799686736","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140606341,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606341},{"feature_type":"variation","strand":1,"alleles":["TTT","T"],"end":140606345,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606343,"clinical_significance":[],"seq_region_name":"7","id":"rs1174206926"},{"end":140606347,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140606347,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs572659476","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799687258","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606349,"feature_type":"variation","strand":1,"end":140606349,"alleles":["T","C"]},{"strand":1,"feature_type":"variation","end":140606353,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606353,"source":"dbSNP","id":"rs1328696001","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1197825468","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140606358,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606358,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs930111150","source":"dbSNP","start":140606360,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140606360,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606368,"source":"dbSNP","strand":1,"feature_type":"variation","end":140606368,"alleles":["C","A"],"id":"rs1799687814","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606376,"feature_type":"variation","strand":1,"end":140606376,"alleles":["A","G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs28459846"},{"end":140606379,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140606379,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs747461951"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1488031192","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606387,"feature_type":"variation","strand":1,"end":140606393,"alleles":["ACATACA","ACA"]},{"id":"rs955389240","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606394,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140606394},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140606398,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606398,"source":"dbSNP","seq_region_name":"7","id":"rs77665018","clinical_significance":[]},{"source":"dbSNP","start":140606411,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["ATAAATAA","ATAA"],"end":140606418,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1346271895"},{"clinical_significance":[],"id":"rs1799688939","seq_region_name":"7","feature_type":"variation","strand":1,"end":140606415,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606415},{"clinical_significance":[],"seq_region_name":"7","id":"rs1303296631","alleles":["T","C"],"end":140606416,"feature_type":"variation","strand":1,"source":"dbSNP","start":140606416,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140606422,"alleles":["AACAAC","AAC"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140606417,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799689151"},{"clinical_significance":[],"id":"rs1449637094","seq_region_name":"7","source":"dbSNP","start":140606419,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140606419,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1228701360","clinical_significance":[],"start":140606420,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140606420,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs944481750","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606421,"source":"dbSNP","strand":1,"feature_type":"variation","end":140606421,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs558365635","clinical_significance":[],"strand":1,"feature_type":"variation","end":140606422,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606422,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs531020105","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606423,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140606423},{"seq_region_name":"7","id":"rs1043603927","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606425,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140606425},{"seq_region_name":"7","id":"rs534227713","clinical_significance":[],"alleles":["A","T"],"end":140606426,"strand":1,"feature_type":"variation","start":140606426,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["G","A","C","T"],"end":140606431,"strand":1,"feature_type":"variation","start":140606431,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1799690000","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs980015081","source":"dbSNP","start":140606438,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140606438,"alleles":["T","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs7794206","clinical_significance":[],"start":140606444,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140606444,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1799690350","clinical_significance":[],"strand":1,"feature_type":"variation","end":140606446,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606446,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs999284243","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606449,"feature_type":"variation","strand":1,"end":140606449,"alleles":["T","C"]},{"clinical_significance":[],"id":"rs1475641516","seq_region_name":"7","alleles":["C","A"],"end":140606455,"feature_type":"variation","strand":1,"source":"dbSNP","start":140606455,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799690620","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606465,"feature_type":"variation","strand":1,"end":140606465,"alleles":["G","A"]},{"start":140606467,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140606467,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs372723853","clinical_significance":[]},{"end":140606470,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140606470,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799690898","clinical_significance":[]},{"start":140606471,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140606471,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","id":"rs536881688","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140606472,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606472,"source":"dbSNP","seq_region_name":"7","id":"rs769598985","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs543818222","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606473,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140606473},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140606475,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606475,"source":"dbSNP","seq_region_name":"7","id":"rs1477581563","clinical_significance":[]},{"seq_region_name":"7","id":"rs549471400","clinical_significance":[],"alleles":["AAGAAGAA","AAGAA"],"end":140606488,"strand":1,"feature_type":"variation","start":140606481,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606483,"source":"dbSNP","strand":1,"feature_type":"variation","end":140606483,"alleles":["G","A"],"seq_region_name":"7","id":"rs1799691465","clinical_significance":[]},{"seq_region_name":"7","id":"rs1013668895","clinical_significance":[],"end":140606497,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140606497,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799691662","feature_type":"variation","strand":1,"end":140606503,"alleles":["TTTT","TTT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606500},{"feature_type":"variation","strand":1,"end":140606505,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606505,"clinical_significance":[],"id":"rs1799691773","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1391903410","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606509,"feature_type":"variation","strand":1,"end":140606509,"alleles":["A","G"]},{"id":"rs1278592805","seq_region_name":"7","clinical_significance":[],"start":140606510,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140606510,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"alleles":["A","G"],"end":140606511,"feature_type":"variation","strand":1,"source":"dbSNP","start":140606511,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1563174667"},{"start":140606517,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140606517,"strand":1,"feature_type":"variation","id":"rs1196866898","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140606523,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606523,"clinical_significance":[],"id":"rs1024172517","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799692367","clinical_significance":[],"end":140606524,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140606524,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["G","C"],"end":140606537,"feature_type":"variation","strand":1,"source":"dbSNP","start":140606537,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1249933348"},{"clinical_significance":[],"seq_region_name":"7","id":"rs549697577","feature_type":"variation","strand":1,"end":140606546,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606546},{"clinical_significance":[],"seq_region_name":"7","id":"rs969402039","source":"dbSNP","start":140606554,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140606554,"alleles":["G","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1339376923","source":"dbSNP","start":140606556,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140606556,"alleles":["T","C"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606557,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140606557,"clinical_significance":[],"seq_region_name":"7","id":"rs1293511423"},{"seq_region_name":"7","id":"rs974094804","clinical_significance":[],"strand":1,"feature_type":"variation","end":140606560,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606560,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs188977153","alleles":["C","T"],"end":140606563,"feature_type":"variation","strand":1,"source":"dbSNP","start":140606563,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606564,"source":"dbSNP","strand":1,"feature_type":"variation","end":140606564,"alleles":["C","G","T"],"seq_region_name":"7","id":"rs1333482643","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799693188","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140606568,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606568},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606571,"feature_type":"variation","strand":1,"end":140606571,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799693286"},{"clinical_significance":[],"id":"rs570913399","seq_region_name":"7","end":140606572,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140606572,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140606573,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140606573,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799693503","clinical_significance":[]},{"start":140606575,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140606575,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799693597","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799693697","clinical_significance":[],"end":140606579,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140606579,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140606581,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606581,"clinical_significance":[],"seq_region_name":"7","id":"rs1336812087"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799693881","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606584,"feature_type":"variation","strand":1,"end":140606584,"alleles":["T","G"]},{"seq_region_name":"7","id":"rs1799693990","clinical_significance":[],"strand":1,"feature_type":"variation","end":140606588,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606588,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1398373734","source":"dbSNP","start":140606589,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140606589,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606592,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140606592,"clinical_significance":[],"id":"rs2130696059","seq_region_name":"7"},{"start":140606596,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140606596,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1165882318","clinical_significance":[]},{"alleles":["CCC","CC"],"end":140606598,"feature_type":"variation","strand":1,"source":"dbSNP","start":140606596,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799694427"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606599,"source":"dbSNP","strand":1,"feature_type":"variation","end":140606599,"alleles":["A","T"],"seq_region_name":"7","id":"rs1799694584","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs766468792","source":"dbSNP","start":140606600,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140606600,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1418932962","end":140606601,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140606601,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1799695000","seq_region_name":"7","clinical_significance":[],"start":140606607,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140606607,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"id":"rs982915032","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606619,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140606619},{"seq_region_name":"7","id":"rs1585744105","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606621,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140606621},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799695291","source":"dbSNP","start":140606624,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140606624,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606625,"feature_type":"variation","strand":1,"end":140606625,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1474297744"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606626,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140606626,"seq_region_name":"7","id":"rs879887807","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140606627,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606627,"clinical_significance":[],"id":"rs1585744138","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140606628,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606628,"source":"dbSNP","seq_region_name":"7","id":"rs1799695651","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799695755","end":140606631,"alleles":["GGGG","GGGGG"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140606628,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs376234445","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606630,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140606630},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799695976","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606631,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140606631},{"clinical_significance":[],"id":"rs1799696071","seq_region_name":"7","source":"dbSNP","start":140606634,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140606634,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs944245962","end":140606639,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140606639,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140606644,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140606644,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799696274"},{"seq_region_name":"7","id":"rs1040117610","clinical_significance":[],"alleles":["T","A"],"end":140606648,"strand":1,"feature_type":"variation","start":140606648,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1799696459","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140606649,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606649,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140606655,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606655,"source":"dbSNP","seq_region_name":"7","id":"rs905117098","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1198474471","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606658,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140606658},{"source":"dbSNP","start":140606659,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140606659,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799696760"},{"source":"dbSNP","start":140606663,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AA","AAA"],"end":140606664,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799696867"},{"end":140606665,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140606665,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799696961","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140606669,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606669,"source":"dbSNP","seq_region_name":"7","id":"rs1234035708","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1006013819","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140606672,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606672},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140606673,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606673,"source":"dbSNP","seq_region_name":"7","id":"rs921707875","clinical_significance":[]},{"seq_region_name":"7","id":"rs148254553","clinical_significance":[],"start":140606674,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140606674,"strand":1,"feature_type":"variation"},{"end":140606676,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140606676,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs541635645"},{"end":140606679,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140606679,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799697620","clinical_significance":[]},{"seq_region_name":"7","id":"rs1354601643","clinical_significance":[],"strand":1,"feature_type":"variation","end":140606680,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606680,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1353669460","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140606681,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606681,"source":"dbSNP"},{"alleles":["G","A"],"end":140606682,"feature_type":"variation","strand":1,"source":"dbSNP","start":140606682,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1208951861"},{"clinical_significance":[],"seq_region_name":"7","id":"rs994241571","source":"dbSNP","start":140606683,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140606683,"feature_type":"variation","strand":1},{"start":140606684,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140606684,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1439445174","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799698232","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606687,"feature_type":"variation","strand":1,"end":140606687,"alleles":["T","C"]},{"end":140606689,"alleles":["TCT","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140606687,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799698334"},{"seq_region_name":"7","id":"rs559945552","clinical_significance":[],"start":140606689,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140606689,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140606720,"alleles":["TGGTCTAAGGAACACCAGGAGATGGTCT","TGGTCT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606693,"clinical_significance":[],"seq_region_name":"7","id":"rs1585744271"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140606697,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606697,"clinical_significance":[],"seq_region_name":"7","id":"rs1251048234"},{"seq_region_name":"7","id":"rs903743617","clinical_significance":[],"alleles":["A","G"],"end":140606699,"strand":1,"feature_type":"variation","start":140606699,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1326764967","seq_region_name":"7","source":"dbSNP","start":140606701,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140606701,"alleles":["G","T"],"feature_type":"variation","strand":1},{"id":"rs1799698910","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140606703,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606703,"source":"dbSNP"},{"id":"rs999399039","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140606704,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606704,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1394922084","clinical_significance":[],"start":140606708,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140606708,"alleles":["C","A","T"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606710,"source":"dbSNP","strand":1,"feature_type":"variation","end":140606710,"alleles":["G","A"],"seq_region_name":"7","id":"rs2130696308","clinical_significance":[]},{"end":140606712,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140606712,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs527482352","seq_region_name":"7"},{"end":140606715,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140606715,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1189526001","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606720,"feature_type":"variation","strand":1,"end":140606720,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799699654"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130696329","feature_type":"variation","strand":1,"alleles":["T","A"],"end":140606721,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606721},{"start":140606722,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140606722,"alleles":["G","T"],"strand":1,"feature_type":"variation","id":"rs955333907","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606731,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140606731,"seq_region_name":"7","id":"rs141266358","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1018491567","source":"dbSNP","start":140606733,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140606733,"feature_type":"variation","strand":1},{"id":"rs570819228","seq_region_name":"7","clinical_significance":[],"end":140606739,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140606739,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140606746,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140606746,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1585744387","seq_region_name":"7"},{"source":"dbSNP","start":140606747,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140606747,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1362631313"},{"start":140606749,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140606749,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799700384","clinical_significance":[]},{"alleles":["A","G"],"end":140606753,"strand":1,"feature_type":"variation","start":140606753,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130696378","clinical_significance":[]},{"clinical_significance":[],"id":"rs1585744405","seq_region_name":"7","alleles":["A","C"],"end":140606754,"feature_type":"variation","strand":1,"source":"dbSNP","start":140606754,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1013864973","feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140606755,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606755},{"clinical_significance":[],"seq_region_name":"7","id":"rs531735114","feature_type":"variation","strand":1,"end":140606759,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606759},{"seq_region_name":"7","id":"rs1799700800","clinical_significance":[],"start":140606760,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140606760,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606762,"feature_type":"variation","strand":1,"end":140606762,"alleles":["A","G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs181068984"},{"id":"rs1215208799","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140606767,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606767,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606771,"source":"dbSNP","strand":1,"feature_type":"variation","end":140606771,"alleles":["G","A","C"],"id":"rs1449459150","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606773,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140606773,"clinical_significance":[],"id":"rs1288686549","seq_region_name":"7"},{"source":"dbSNP","start":140606775,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C","T"],"end":140606775,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs568786891"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606776,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140606776,"id":"rs925434692","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799701773","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606778,"feature_type":"variation","strand":1,"end":140606778,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1412039382","clinical_significance":[],"start":140606780,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140606780,"alleles":["G","A","C"],"strand":1,"feature_type":"variation"},{"id":"rs1799702088","seq_region_name":"7","clinical_significance":[],"start":140606782,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140606782,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585744490","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606783,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140606783},{"clinical_significance":[],"id":"rs536189427","seq_region_name":"7","alleles":["C","A","T"],"end":140606784,"feature_type":"variation","strand":1,"source":"dbSNP","start":140606784,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140606787,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140606787,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799702571"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606789,"source":"dbSNP","strand":1,"feature_type":"variation","end":140606789,"alleles":["G","A"],"seq_region_name":"7","id":"rs1434595091","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs987831029","source":"dbSNP","start":140606792,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140606792,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1799702975","clinical_significance":[],"start":140606795,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140606795,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606796,"source":"dbSNP","strand":1,"feature_type":"variation","end":140606796,"alleles":["C","A"],"seq_region_name":"7","id":"rs1799703101","clinical_significance":[]},{"id":"rs1349572448","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606797,"source":"dbSNP","strand":1,"feature_type":"variation","end":140606797,"alleles":["C","A"]},{"source":"dbSNP","start":140606798,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140606798,"alleles":["T","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs546949104"},{"seq_region_name":"7","id":"rs1026996134","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140606801,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606801,"source":"dbSNP"},{"id":"rs1799703690","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606813,"source":"dbSNP","strand":1,"feature_type":"variation","end":140606813,"alleles":["C","T"]},{"feature_type":"variation","strand":1,"end":140606815,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606815,"clinical_significance":[],"id":"rs1799703816","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140606816,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606816,"clinical_significance":[],"seq_region_name":"7","id":"rs754778427"},{"end":140606823,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140606823,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs369452568","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606831,"source":"dbSNP","strand":1,"feature_type":"variation","end":140606831,"alleles":["C","A"],"id":"rs554483294","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140606834,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606834,"clinical_significance":[],"seq_region_name":"7","id":"rs781137554"},{"alleles":["C","A","T"],"end":140606837,"feature_type":"variation","strand":1,"source":"dbSNP","start":140606837,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1382851639"},{"clinical_significance":[],"seq_region_name":"7","id":"rs951572337","source":"dbSNP","start":140606839,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140606839,"alleles":["C","T"],"feature_type":"variation","strand":1},{"end":140606841,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140606841,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799704888","clinical_significance":[]},{"source":"dbSNP","start":140606842,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140606842,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs949023596"},{"strand":1,"feature_type":"variation","end":140606844,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606844,"source":"dbSNP","seq_region_name":"7","id":"rs1799705190","clinical_significance":[]},{"source":"dbSNP","start":140606845,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140606847,"alleles":["AAA","AA"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1455052955"},{"seq_region_name":"7","id":"rs1799705482","clinical_significance":[],"end":140606846,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140606846,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140606852,"alleles":["A","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606852,"source":"dbSNP","seq_region_name":"7","id":"rs184705043","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799705833","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140606853,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606853,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1192218034","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","TT"],"end":140606854,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606854,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1477904105","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606856,"source":"dbSNP","strand":1,"feature_type":"variation","end":140606856,"alleles":["A","T"]},{"end":140606861,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140606861,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs539635667","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606862,"source":"dbSNP","strand":1,"feature_type":"variation","end":140606862,"alleles":["T","C"],"seq_region_name":"7","id":"rs1216041692","clinical_significance":[]},{"end":140606866,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140606866,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs150790088","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1215817711","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606874,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140606874},{"id":"rs1799706901","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140606879,"strand":1,"feature_type":"variation","start":140606879,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606882,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140606882,"clinical_significance":[],"seq_region_name":"7","id":"rs1348426918"},{"feature_type":"variation","strand":1,"end":140606889,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606889,"clinical_significance":[],"seq_region_name":"7","id":"rs941936571"},{"start":140606890,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140606890,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1037655908","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606891,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140606891,"seq_region_name":"7","id":"rs1585744681","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs139200384","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140606892,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606892},{"id":"rs1585744695","seq_region_name":"7","clinical_significance":[],"start":140606896,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140606896,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799707939","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140606904,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606904},{"seq_region_name":"7","id":"rs1217326445","clinical_significance":[],"start":140606908,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140606908,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1799708206","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140606911,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606911},{"seq_region_name":"7","id":"rs1366602159","clinical_significance":[],"strand":1,"feature_type":"variation","end":140606920,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606920,"source":"dbSNP"},{"end":140606921,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140606921,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799708350"},{"id":"rs1799708491","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606922,"source":"dbSNP","strand":1,"feature_type":"variation","end":140606922,"alleles":["C","A"]},{"clinical_significance":[],"id":"rs2130696659","seq_region_name":"7","end":140606925,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140606925,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606931,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140606931,"clinical_significance":[],"seq_region_name":"7","id":"rs544214062"},{"strand":1,"feature_type":"variation","end":140606932,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606932,"source":"dbSNP","seq_region_name":"7","id":"rs1799708753","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140606933,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606933,"source":"dbSNP","seq_region_name":"7","id":"rs1764214580","clinical_significance":[]},{"end":140606934,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140606934,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs80292212","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606939,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140606939,"clinical_significance":[],"seq_region_name":"7","id":"rs574077650"},{"alleles":["T","C"],"end":140606940,"feature_type":"variation","strand":1,"source":"dbSNP","start":140606940,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1047148294"},{"clinical_significance":[],"id":"rs1799709409","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606941,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140606941},{"feature_type":"variation","strand":1,"end":140606948,"alleles":["G","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606948,"clinical_significance":[],"seq_region_name":"7","id":"rs1297582990"},{"source":"dbSNP","start":140606952,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140606952,"alleles":["A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799709722"},{"start":140606973,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140606973,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1377869568","clinical_significance":[]},{"seq_region_name":"7","id":"rs1172283714","clinical_significance":[],"start":140606975,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140606975,"strand":1,"feature_type":"variation"},{"alleles":["C","G","T"],"end":140606976,"feature_type":"variation","strand":1,"source":"dbSNP","start":140606976,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1414309897","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799710338","clinical_significance":[],"end":140606982,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140606982,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140606983,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140606983,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs891222139","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1008190793","alleles":["C","G"],"end":140606989,"feature_type":"variation","strand":1,"source":"dbSNP","start":140606989,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140606990,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140606990,"source":"dbSNP","id":"rs747776894","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606993,"feature_type":"variation","strand":1,"end":140606993,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585744803"},{"end":140606994,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140606994,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799711077","seq_region_name":"7"},{"clinical_significance":[],"id":"rs188677653","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606995,"feature_type":"variation","strand":1,"end":140606995,"alleles":["G","A"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606997,"feature_type":"variation","strand":1,"end":140606997,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1476154044"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1260431277","feature_type":"variation","strand":1,"end":140606998,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140606998},{"seq_region_name":"7","id":"rs964110839","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140607001,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607001,"source":"dbSNP"},{"source":"dbSNP","start":140607002,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140607002,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs565685182"},{"strand":1,"feature_type":"variation","end":140607005,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607005,"source":"dbSNP","seq_region_name":"7","id":"rs1799711844","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799711997","end":140607012,"alleles":["TTCTTCT","TTCT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140607006,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1799712157","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607008,"source":"dbSNP","strand":1,"feature_type":"variation","end":140607008,"alleles":["C","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607014,"feature_type":"variation","strand":1,"end":140607014,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1032618164"},{"clinical_significance":[],"seq_region_name":"7","id":"rs979025097","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140607018,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607018},{"feature_type":"variation","strand":1,"end":140607019,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607019,"clinical_significance":[],"seq_region_name":"7","id":"rs560008289"},{"id":"rs1207903005","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140607020,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607020,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs956842020","feature_type":"variation","strand":1,"alleles":["T","A"],"end":140607021,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607021},{"end":140607025,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140607025,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs924946582"},{"alleles":["A","G"],"end":140607026,"strand":1,"feature_type":"variation","start":140607026,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1563174951","clinical_significance":[]},{"clinical_significance":[],"id":"rs988276333","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","A"],"end":140607035,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607035},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607042,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140607042,"id":"rs1799713424","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140607045,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C","G"],"end":140607045,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799713577"},{"source":"dbSNP","start":140607048,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140607048,"alleles":["A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799713730"},{"clinical_significance":[],"id":"rs917628181","seq_region_name":"7","feature_type":"variation","strand":1,"end":140607049,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607049},{"clinical_significance":[],"seq_region_name":"7","id":"rs1485961246","source":"dbSNP","start":140607050,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140607050,"alleles":["A","C"],"feature_type":"variation","strand":1},{"alleles":["G","A"],"end":140607052,"strand":1,"feature_type":"variation","start":140607052,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs970448961","clinical_significance":[]},{"seq_region_name":"7","id":"rs1253491302","clinical_significance":[],"start":140607057,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140607057,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"start":140607058,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140607058,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1357425834","clinical_significance":[]},{"alleles":["T","C"],"end":140607060,"strand":1,"feature_type":"variation","start":140607060,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799714610","clinical_significance":[]},{"id":"rs1422839542","seq_region_name":"7","clinical_significance":[],"end":140607069,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140607069,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563174972","end":140607072,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140607072,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607074,"feature_type":"variation","strand":1,"end":140607074,"alleles":["T","G"],"clinical_significance":[],"id":"rs1052291424","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607075,"source":"dbSNP","strand":1,"feature_type":"variation","end":140607075,"alleles":["C","T"],"seq_region_name":"7","id":"rs980583927","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799715293","feature_type":"variation","strand":1,"end":140607080,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607080},{"id":"rs1193416655","seq_region_name":"7","clinical_significance":[],"alleles":["A","C","G"],"end":140607081,"strand":1,"feature_type":"variation","start":140607081,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1799715644","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607082,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140607082},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607083,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140607083,"seq_region_name":"7","id":"rs1799715786","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799715930","feature_type":"variation","strand":1,"end":140607086,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607086},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607092,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140607092,"seq_region_name":"7","id":"rs1799716077","clinical_significance":[]},{"end":140607095,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140607095,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1447898187"},{"feature_type":"variation","strand":1,"end":140607096,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607096,"clinical_significance":[],"seq_region_name":"7","id":"rs1799716352"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799716499","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607098,"feature_type":"variation","strand":1,"end":140607098,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs147256258","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140607103,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607103},{"clinical_significance":[],"seq_region_name":"7","id":"rs941730681","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607104,"feature_type":"variation","strand":1,"end":140607104,"alleles":["G","A","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607105,"source":"dbSNP","strand":1,"feature_type":"variation","end":140607105,"alleles":["T","A"],"id":"rs1167181218","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140607106,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607106,"clinical_significance":[],"seq_region_name":"7","id":"rs755778058"},{"end":140607108,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140607108,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs373479141","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs73736640","feature_type":"variation","strand":1,"end":140607109,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607109},{"clinical_significance":[],"id":"rs531679383","seq_region_name":"7","source":"dbSNP","start":140607114,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140607114,"alleles":["C","T"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140607115,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607115,"clinical_significance":[],"seq_region_name":"7","id":"rs1051598564"},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140607121,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607121,"source":"dbSNP","seq_region_name":"7","id":"rs1482848695","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799718187","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607124,"feature_type":"variation","strand":1,"end":140607124,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs890330820","clinical_significance":[],"end":140607125,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140607125,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["C","A"],"end":140607126,"strand":1,"feature_type":"variation","start":140607126,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1799718522","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140607130,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140607130,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799718680"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799718843","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140607132,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607132},{"id":"rs1206445778","seq_region_name":"7","clinical_significance":[],"alleles":["C","A"],"end":140607133,"strand":1,"feature_type":"variation","start":140607133,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs117946586","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607135,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140607135},{"clinical_significance":[],"seq_region_name":"7","id":"rs558295503","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607136,"feature_type":"variation","strand":1,"end":140607136,"alleles":["C","T"]},{"clinical_significance":[],"id":"rs1257723638","seq_region_name":"7","alleles":["CTTCTTC","CTTC"],"end":140607142,"feature_type":"variation","strand":1,"source":"dbSNP","start":140607136,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1799720684","seq_region_name":"7","end":140607138,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140607138,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","T"],"end":140607139,"feature_type":"variation","strand":1,"source":"dbSNP","start":140607139,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1337087016"},{"clinical_significance":[],"id":"rs1799721002","seq_region_name":"7","source":"dbSNP","start":140607142,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140607142,"alleles":["C","A"],"feature_type":"variation","strand":1},{"end":140607143,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140607143,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs899812941","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607148,"source":"dbSNP","strand":1,"feature_type":"variation","end":140607148,"alleles":["C","T"],"seq_region_name":"7","id":"rs1585745132","clinical_significance":[]},{"id":"rs1799721485","seq_region_name":"7","clinical_significance":[],"alleles":["CC","C"],"end":140607149,"strand":1,"feature_type":"variation","start":140607148,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607156,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140607156,"clinical_significance":[],"seq_region_name":"7","id":"rs1799721654"},{"alleles":["C","A"],"end":140607160,"feature_type":"variation","strand":1,"source":"dbSNP","start":140607160,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1004247202","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130697044","alleles":["C","T"],"end":140607161,"feature_type":"variation","strand":1,"source":"dbSNP","start":140607161,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs529300582","source":"dbSNP","start":140607162,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140607162,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1300408780","source":"dbSNP","start":140607164,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140607164,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140607165,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607165,"clinical_significance":[],"seq_region_name":"7","id":"rs1328488960"},{"seq_region_name":"7","id":"rs548149150","clinical_significance":[],"strand":1,"feature_type":"variation","end":140607166,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607166,"source":"dbSNP"},{"source":"dbSNP","start":140607175,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140607175,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs746381743"},{"seq_region_name":"7","id":"rs1799722876","clinical_significance":[],"alleles":["C","T"],"end":140607183,"strand":1,"feature_type":"variation","start":140607183,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1032973480","source":"dbSNP","start":140607187,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140607187,"alleles":["T","C","G"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["GATGGGATGG","GATGG"],"end":140607201,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607192,"source":"dbSNP","id":"rs1348440001","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140607194,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140607194,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1330288100","seq_region_name":"7"},{"seq_region_name":"7","id":"rs966025082","clinical_significance":[],"start":140607195,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140607195,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs763792479","clinical_significance":[],"end":140607197,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140607197,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140607199,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140607199,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799723856","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799724026","clinical_significance":[],"alleles":["G","A"],"end":140607200,"strand":1,"feature_type":"variation","start":140607200,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130697101","feature_type":"variation","strand":1,"end":140607202,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607202},{"end":140607206,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140607206,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1369700234"},{"seq_region_name":"7","id":"rs975571295","clinical_significance":[],"end":140607207,"alleles":["T","C","G"],"strand":1,"feature_type":"variation","start":140607207,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140607210,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607210,"source":"dbSNP","seq_region_name":"7","id":"rs1408681451","clinical_significance":[]},{"start":140607211,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140607211,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs1254218812","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1028910472","clinical_significance":[],"start":140607220,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140607220,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140607221,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140607221,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs956955801","seq_region_name":"7"},{"end":140607222,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140607222,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs566336168","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607224,"feature_type":"variation","strand":1,"end":140607224,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1263892377"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607228,"feature_type":"variation","strand":1,"end":140607228,"alleles":["C","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1025091146"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607229,"source":"dbSNP","strand":1,"feature_type":"variation","end":140607229,"alleles":["T","A"],"seq_region_name":"7","id":"rs554122712","clinical_significance":[]},{"id":"rs540023842","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607238,"source":"dbSNP","strand":1,"feature_type":"variation","end":140607238,"alleles":["C","T"]},{"end":140607239,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140607239,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs988231521","clinical_significance":[]},{"source":"dbSNP","start":140607241,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140607241,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs775777299"},{"alleles":["T","C"],"end":140607242,"feature_type":"variation","strand":1,"source":"dbSNP","start":140607242,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799725577"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140607244,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607244,"source":"dbSNP","id":"rs970900715","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607246,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140607246,"clinical_significance":[],"seq_region_name":"7","id":"rs181462646"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140607249,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607249,"clinical_significance":[],"id":"rs1799725855","seq_region_name":"7"},{"seq_region_name":"7","id":"rs570541452","clinical_significance":[],"strand":1,"feature_type":"variation","end":140607252,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607252,"source":"dbSNP"},{"end":140607254,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140607254,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1392506552"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799726179","source":"dbSNP","start":140607255,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140607255,"alleles":["G","A"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140607263,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140607263,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1455008784"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607268,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140607268,"id":"rs931169611","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607270,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140607270,"clinical_significance":[],"seq_region_name":"7","id":"rs1799726501"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607273,"feature_type":"variation","strand":1,"end":140607273,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799726602"},{"start":140607276,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140607276,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799726715","clinical_significance":[]},{"seq_region_name":"7","id":"rs963346853","clinical_significance":[],"strand":1,"feature_type":"variation","end":140607277,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607277,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799726913","clinical_significance":[],"strand":1,"feature_type":"variation","end":140607284,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607284,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1048498067","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607286,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140607286},{"id":"rs1178838833","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140607300,"alleles":["AAGGAGAGGAAGG","AAGG"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607288,"source":"dbSNP"},{"clinical_significance":[],"id":"rs973097918","seq_region_name":"7","alleles":["G","A"],"end":140607290,"feature_type":"variation","strand":1,"source":"dbSNP","start":140607290,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1160416475","seq_region_name":"7","source":"dbSNP","start":140607291,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140607291,"alleles":["G","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1437678620","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607293,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140607293},{"end":140607295,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140607295,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1379472130","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799727842","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607298,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AGGGAGG","AGG"],"end":140607304},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799728010","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607299,"feature_type":"variation","strand":1,"end":140607299,"alleles":["G","A"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607300,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140607300,"seq_region_name":"7","id":"rs1799728184","clinical_significance":[]},{"clinical_significance":[],"id":"rs887216963","seq_region_name":"7","source":"dbSNP","start":140607301,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140607301,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1799728494","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607305,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140607305},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607311,"source":"dbSNP","strand":1,"feature_type":"variation","end":140607317,"alleles":["AGAGAGA","AGA"],"seq_region_name":"7","id":"rs1434687228","clinical_significance":[]},{"seq_region_name":"7","id":"rs1004185110","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607319,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AGAGA","AGA"],"end":140607323},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607322,"feature_type":"variation","strand":1,"end":140607322,"alleles":["G","T"],"clinical_significance":[],"id":"rs537576854","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607323,"feature_type":"variation","strand":1,"alleles":["AAAAA","AAAAAAA"],"end":140607327,"clinical_significance":[],"seq_region_name":"7","id":"rs1799729111"},{"alleles":["A","T"],"end":140607326,"feature_type":"variation","strand":1,"source":"dbSNP","start":140607326,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799729262","seq_region_name":"7"},{"id":"rs1159220919","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607331,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140607331},{"seq_region_name":"7","id":"rs1799729586","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607333,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140607333},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607335,"source":"dbSNP","strand":1,"feature_type":"variation","end":140607335,"alleles":["A","G"],"seq_region_name":"7","id":"rs1799729719","clinical_significance":[]},{"alleles":["A","G"],"end":140607337,"strand":1,"feature_type":"variation","start":140607337,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799729814","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","C","G","T"],"end":140607344,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607344,"clinical_significance":[],"seq_region_name":"7","id":"rs1486246510"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1215090507","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140607346,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607346},{"start":140607346,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["GGGTAACAAA","GGGTAACAAAGGGTAACAAA"],"end":140607355,"strand":1,"feature_type":"variation","id":"rs1799730155","seq_region_name":"7","clinical_significance":[]},{"id":"rs919134822","seq_region_name":"7","clinical_significance":[],"start":140607348,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140607348,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1041449021","clinical_significance":[],"start":140607350,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140607350,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1433195518","clinical_significance":[],"start":140607352,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140607352,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1319599081","end":140607353,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140607353,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1799730653","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607356,"source":"dbSNP","strand":1,"feature_type":"variation","end":140607356,"alleles":["T","A"]},{"alleles":["C","T"],"end":140607360,"strand":1,"feature_type":"variation","start":140607360,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1329690290","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140607365,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607365,"clinical_significance":[],"seq_region_name":"7","id":"rs1799730845"},{"seq_region_name":"7","id":"rs1371422309","clinical_significance":[],"strand":1,"feature_type":"variation","end":140607366,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607366,"source":"dbSNP"},{"id":"rs555840009","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607367,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140607367},{"seq_region_name":"7","id":"rs1385839687","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607374,"source":"dbSNP","strand":1,"feature_type":"variation","end":140607374,"alleles":["G","C"]},{"seq_region_name":"7","id":"rs1799731373","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607378,"source":"dbSNP","strand":1,"feature_type":"variation","end":140607377,"alleles":["-","TAGAGTCATAG"]},{"seq_region_name":"7","id":"rs1362048704","clinical_significance":[],"strand":1,"feature_type":"variation","end":140607385,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607385,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs185755374","source":"dbSNP","start":140607386,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140607386,"alleles":["C","T"],"feature_type":"variation","strand":1},{"id":"rs1799731664","seq_region_name":"7","clinical_significance":[],"alleles":["G","C"],"end":140607394,"strand":1,"feature_type":"variation","start":140607394,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799731757","alleles":["C","-"],"end":140607395,"feature_type":"variation","strand":1,"source":"dbSNP","start":140607395,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1299438576","clinical_significance":[],"start":140607398,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140607398,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140607404,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607404,"source":"dbSNP","seq_region_name":"7","id":"rs574137747","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607407,"feature_type":"variation","strand":1,"end":140607407,"alleles":["C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799732058"},{"source":"dbSNP","start":140607409,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140607409,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1299088761"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1051713704","feature_type":"variation","strand":1,"end":140607410,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607410},{"seq_region_name":"7","id":"rs1799732357","clinical_significance":[],"strand":1,"feature_type":"variation","end":140607412,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607412,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140607413,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607413,"clinical_significance":[],"id":"rs997503444","seq_region_name":"7"},{"end":140607422,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140607422,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs768800691","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799732684","clinical_significance":[],"alleles":["C","T"],"end":140607423,"strand":1,"feature_type":"variation","start":140607423,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607424,"feature_type":"variation","strand":1,"end":140607435,"alleles":["TGTGTGTGTGTG","TGTGTGTGTG","TGTGTGTGTGTGTG"],"clinical_significance":[],"seq_region_name":"7","id":"rs142708944"},{"end":140607425,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140607425,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799732948"},{"seq_region_name":"7","id":"rs1000343615","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140607426,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607426,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1429271201","feature_type":"variation","strand":1,"end":140607430,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607430},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607431,"source":"dbSNP","strand":1,"feature_type":"variation","end":140607431,"alleles":["G","A"],"seq_region_name":"7","id":"rs1799733256","clinical_significance":[]},{"clinical_significance":[],"id":"rs1032028034","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607433,"feature_type":"variation","strand":1,"end":140607433,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs377034762","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140607434,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607434,"source":"dbSNP"},{"source":"dbSNP","start":140607435,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140607435,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1488000910"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607436,"source":"dbSNP","strand":1,"feature_type":"variation","end":140607436,"alleles":["G","T"],"seq_region_name":"7","id":"rs1799733593","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs776750076","source":"dbSNP","start":140607437,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140607437,"alleles":["G","C"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140607439,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607439,"source":"dbSNP","seq_region_name":"7","id":"rs1799733818","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799733904","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140607444,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607444,"source":"dbSNP"},{"source":"dbSNP","start":140607445,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140607445,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1202652263"},{"seq_region_name":"7","id":"rs116718833","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607450,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140607450},{"seq_region_name":"7","id":"rs1207673906","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607460,"source":"dbSNP","strand":1,"feature_type":"variation","end":140607460,"alleles":["G","A"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607461,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140607461,"clinical_significance":[],"seq_region_name":"7","id":"rs1799734371"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1255707472","source":"dbSNP","start":140607462,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140607462,"alleles":["C","T"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140607466,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607466,"clinical_significance":[],"seq_region_name":"7","id":"rs1799734481"},{"start":140607468,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C","G"],"end":140607468,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799734591","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607469,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140607469,"clinical_significance":[],"seq_region_name":"7","id":"rs190561838"},{"alleles":["G","A"],"end":140607470,"strand":1,"feature_type":"variation","start":140607470,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1253287684","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140607471,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607471,"source":"dbSNP","id":"rs1799734923","seq_region_name":"7","clinical_significance":[]},{"id":"rs970459369","seq_region_name":"7","clinical_significance":[],"start":140607474,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140607474,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"start":140607475,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140607475,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs181949638","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140607481,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607481,"source":"dbSNP","id":"rs926557875","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799735398","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607486,"source":"dbSNP","strand":1,"feature_type":"variation","end":140607486,"alleles":["C","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1469176620","source":"dbSNP","start":140607487,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140607487,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1397668588","clinical_significance":[],"strand":1,"feature_type":"variation","end":140607488,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607488,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607491,"feature_type":"variation","strand":1,"end":140607491,"alleles":["C","T"],"clinical_significance":[],"id":"rs1799735718","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607495,"feature_type":"variation","strand":1,"end":140607495,"alleles":["C","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799735824"},{"clinical_significance":[],"seq_region_name":"7","id":"rs545995652","source":"dbSNP","start":140607497,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140607497,"alleles":["A","G"],"feature_type":"variation","strand":1},{"end":140607508,"alleles":["CAGCACCAG","CAG"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140607500,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799736030","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607502,"feature_type":"variation","strand":1,"end":140607502,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs564161322"},{"seq_region_name":"7","id":"rs1462291345","clinical_significance":[],"start":140607503,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140607503,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140607509,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607509,"source":"dbSNP","seq_region_name":"7","id":"rs1053712458","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1048278395","source":"dbSNP","start":140607510,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140607510,"feature_type":"variation","strand":1},{"end":140607511,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140607511,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1168753806"},{"clinical_significance":[],"id":"rs2130697663","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607513,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140607513},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607515,"feature_type":"variation","strand":1,"end":140607515,"alleles":["T","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs908591581"},{"alleles":["G","A"],"end":140607516,"strand":1,"feature_type":"variation","start":140607516,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1258268329","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs892501816","end":140607517,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140607517,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs140811959","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607519,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140607519},{"clinical_significance":[],"id":"rs1182557230","seq_region_name":"7","source":"dbSNP","start":140607522,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140607522,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs144748296","source":"dbSNP","start":140607524,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140607524,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799737343","feature_type":"variation","strand":1,"end":140607527,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607527},{"start":140607528,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140607528,"strand":1,"feature_type":"variation","id":"rs1799737735","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140607529,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607529,"clinical_significance":[],"seq_region_name":"7","id":"rs1196814447"},{"id":"rs1799737942","seq_region_name":"7","clinical_significance":[],"start":140607532,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140607532,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"end":140607536,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140607536,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs906673143","clinical_significance":[]},{"seq_region_name":"7","id":"rs1002391499","clinical_significance":[],"start":140607543,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140607543,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1259640862","feature_type":"variation","strand":1,"end":140607550,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607550},{"strand":1,"feature_type":"variation","end":140607552,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607552,"source":"dbSNP","seq_region_name":"7","id":"rs1799738329","clinical_significance":[]},{"seq_region_name":"7","id":"rs1216355221","clinical_significance":[],"start":140607558,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140607558,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"id":"rs1455748536","seq_region_name":"7","clinical_significance":[],"alleles":["C","A","T"],"end":140607559,"strand":1,"feature_type":"variation","start":140607559,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs562154429","end":140607560,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140607560,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799738766","source":"dbSNP","start":140607563,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140607563,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140607564,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607564,"clinical_significance":[],"seq_region_name":"7","id":"rs1799738842"},{"strand":1,"feature_type":"variation","end":140607567,"alleles":["CCCC","CCC"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607564,"source":"dbSNP","seq_region_name":"7","id":"rs1799738942","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607565,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140607565,"seq_region_name":"7","id":"rs1799739037","clinical_significance":[]},{"end":140607566,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140607566,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799739129","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140607567,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607567,"source":"dbSNP","seq_region_name":"7","id":"rs761638006","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140607568,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607568,"clinical_significance":[],"seq_region_name":"7","id":"rs1246916372"},{"feature_type":"variation","strand":1,"end":140607569,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607569,"clinical_significance":[],"id":"rs1799739391","seq_region_name":"7"},{"source":"dbSNP","start":140607571,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140607571,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1338688082"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607572,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140607572,"clinical_significance":[],"seq_region_name":"7","id":"rs1799739553"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140607575,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607575,"source":"dbSNP","id":"rs963160022","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140607580,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607580,"source":"dbSNP","seq_region_name":"7","id":"rs2130697788","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585745985","end":140607581,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140607581,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs529314573","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607582,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140607582},{"clinical_significance":[],"seq_region_name":"7","id":"rs1459246428","end":140607583,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140607583,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs536740747","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140607584,"strand":1,"feature_type":"variation","start":140607584,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1418684797","seq_region_name":"7","clinical_significance":[],"start":140607592,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140607592,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"id":"rs901159344","seq_region_name":"7","clinical_significance":[],"start":140607598,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140607598,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607599,"source":"dbSNP","strand":1,"feature_type":"variation","end":140607599,"alleles":["C","T"],"seq_region_name":"7","id":"rs1471850573","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130697830","source":"dbSNP","start":140607602,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140607602,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585746065","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140607603,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607603},{"clinical_significance":[],"seq_region_name":"7","id":"rs973597607","feature_type":"variation","strand":1,"end":140607608,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607608},{"seq_region_name":"7","id":"rs1799740703","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607608,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CCTTTC","-"],"end":140607613},{"seq_region_name":"7","id":"rs1025975455","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607609,"source":"dbSNP","strand":1,"feature_type":"variation","end":140607609,"alleles":["C","G"]},{"end":140607611,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140607611,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799740868","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140607615,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607615,"clinical_significance":[],"id":"rs1799740950","seq_region_name":"7"},{"start":140607619,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140607619,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1183143161","clinical_significance":[]},{"source":"dbSNP","start":140607621,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140607621,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799741146"},{"start":140607628,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140607628,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs996885957","clinical_significance":[]},{"id":"rs950391753","seq_region_name":"7","clinical_significance":[],"start":140607629,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140607629,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs2130697898","clinical_significance":[],"start":140607635,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140607635,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799741424","end":140607640,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140607640,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs987367115","seq_region_name":"7","clinical_significance":[],"end":140607641,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140607641,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs911829258","clinical_significance":[],"alleles":["C","A"],"end":140607645,"strand":1,"feature_type":"variation","start":140607645,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140607647,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140607647,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs904802070","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1211184988","source":"dbSNP","start":140607652,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140607652,"feature_type":"variation","strand":1},{"start":140607659,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140607659,"alleles":["G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130697931","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607660,"feature_type":"variation","strand":1,"end":140607660,"alleles":["C","A","T"],"clinical_significance":[],"id":"rs1290178318","seq_region_name":"7"},{"end":140607666,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140607666,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130697949","clinical_significance":[]},{"start":140607679,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140607679,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs560107739","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799742066","end":140607680,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140607680,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","T"],"end":140607682,"strand":1,"feature_type":"variation","start":140607682,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799742149","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799742254","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607686,"feature_type":"variation","strand":1,"end":140607686,"alleles":["T","C"]},{"end":140607696,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140607696,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs761748497","clinical_significance":[]},{"start":140607697,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140607697,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs974605937","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140607698,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607698,"clinical_significance":[],"seq_region_name":"7","id":"rs1348057537"},{"end":140607706,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140607706,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1227304874","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799742783","clinical_significance":[],"end":140607709,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140607709,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1000291861","seq_region_name":"7","clinical_significance":[],"start":140607711,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140607711,"alleles":["T","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs925818757","alleles":["T","C"],"end":140607713,"feature_type":"variation","strand":1,"source":"dbSNP","start":140607713,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607714,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140607714,"clinical_significance":[],"seq_region_name":"7","id":"rs765437244"},{"seq_region_name":"7","id":"rs1031809127","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607717,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140607717},{"seq_region_name":"7","id":"rs147925625","clinical_significance":[],"start":140607718,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140607718,"alleles":["G","A","C"],"strand":1,"feature_type":"variation"},{"id":"rs1799743427","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140607726,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607726,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1053828094","source":"dbSNP","start":140607738,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C","G"],"end":140607738,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140607744,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140607744,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs892451048"},{"alleles":["G","A"],"end":140607745,"feature_type":"variation","strand":1,"source":"dbSNP","start":140607745,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs375181638","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1159683253","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607757,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140607757},{"start":140607759,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140607759,"alleles":["C","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799743994","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799744105","clinical_significance":[],"start":140607760,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140607760,"alleles":["C","A","T"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607766,"feature_type":"variation","strand":1,"end":140607766,"alleles":["C","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799744249"},{"feature_type":"variation","strand":1,"alleles":["CACCACCGCCACCACCCTCCACAC","CACCACCGCCACCACCCTCCACACCACCGCCACCACCCTCCACAC"],"end":140607790,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607767,"clinical_significance":[],"seq_region_name":"7","id":"rs1442011289"},{"seq_region_name":"7","id":"rs552032931","clinical_significance":[],"start":140607768,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140607768,"alleles":["A","C","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1799744618","clinical_significance":[],"alleles":["C","T"],"end":140607770,"strand":1,"feature_type":"variation","start":140607770,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799744728","source":"dbSNP","start":140607773,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140607773,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140607774,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607774,"clinical_significance":[],"id":"rs73736641","seq_region_name":"7"},{"clinical_significance":[],"id":"rs537644804","seq_region_name":"7","source":"dbSNP","start":140607776,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140607776,"feature_type":"variation","strand":1},{"id":"rs1799745108","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607778,"source":"dbSNP","strand":1,"feature_type":"variation","end":140607778,"alleles":["C","T"]},{"feature_type":"variation","strand":1,"alleles":["CC","C"],"end":140607779,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607778,"clinical_significance":[],"seq_region_name":"7","id":"rs1799745206"},{"seq_region_name":"7","id":"rs148972545","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140607781,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607781,"source":"dbSNP"},{"source":"dbSNP","start":140607788,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140607788,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs567772433"},{"seq_region_name":"7","id":"rs2130698130","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607791,"source":"dbSNP","strand":1,"feature_type":"variation","end":140607791,"alleles":["A","T"]},{"clinical_significance":[],"id":"rs1799745481","seq_region_name":"7","alleles":["A","C"],"end":140607797,"feature_type":"variation","strand":1,"source":"dbSNP","start":140607797,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140607801,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607801,"source":"dbSNP","seq_region_name":"7","id":"rs187409907","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799745671","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140607802,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607802},{"seq_region_name":"7","id":"rs1288443498","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607803,"source":"dbSNP","strand":1,"feature_type":"variation","end":140607803,"alleles":["C","T"]},{"end":140607805,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140607805,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1799745873","seq_region_name":"7","clinical_significance":[]},{"id":"rs558726935","seq_region_name":"7","clinical_significance":[],"end":140607806,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140607806,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1355842194","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607811,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140607811},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607818,"feature_type":"variation","strand":1,"end":140607818,"alleles":["G","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1283794976"},{"start":140607823,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140607823,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1239212213","clinical_significance":[]},{"source":"dbSNP","start":140607824,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140607824,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1368018352"},{"end":140607825,"alleles":["A","G","T"],"strand":1,"feature_type":"variation","start":140607825,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs115343909","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799749445","seq_region_name":"7","feature_type":"variation","strand":1,"end":140607827,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607827},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607828,"source":"dbSNP","strand":1,"feature_type":"variation","end":140607828,"alleles":["A","C"],"seq_region_name":"7","id":"rs1434527164","clinical_significance":[]},{"end":140607830,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140607830,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs571992897"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1425798174","end":140607831,"alleles":["CC","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140607830,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs2130698204","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607832,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140607832},{"clinical_significance":[],"id":"rs1585746494","seq_region_name":"7","alleles":["G","A"],"end":140607833,"feature_type":"variation","strand":1,"source":"dbSNP","start":140607833,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140607834,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607834,"clinical_significance":[],"seq_region_name":"7","id":"rs1298822038"},{"clinical_significance":[],"seq_region_name":"7","id":"rs767444253","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607835,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140607835},{"seq_region_name":"7","id":"rs1162377852","clinical_significance":[],"strand":1,"feature_type":"variation","end":140607845,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607845,"source":"dbSNP"},{"end":140607849,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140607849,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1421574465","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799750407","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140607856,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607856,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1359259054","clinical_significance":[],"alleles":["GG","G"],"end":140607868,"strand":1,"feature_type":"variation","start":140607867,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1799750610","clinical_significance":[],"start":140607871,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140607871,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"id":"rs1349125051","seq_region_name":"7","clinical_significance":[],"end":140607872,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140607872,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799750827","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140607873,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607873},{"seq_region_name":"7","id":"rs922733030","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140607881,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607881,"source":"dbSNP"},{"start":140607885,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140607885,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799751038","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140607893,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607893,"clinical_significance":[],"id":"rs1799751144","seq_region_name":"7"},{"alleles":["G","T"],"end":140607898,"strand":1,"feature_type":"variation","start":140607898,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1026092647","clinical_significance":[]},{"clinical_significance":[],"id":"rs1435781818","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","T"],"end":140607900,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607900},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799751451","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607904,"feature_type":"variation","strand":1,"end":140607904,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799751570","source":"dbSNP","start":140607905,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140607905,"alleles":["C","T"],"feature_type":"variation","strand":1},{"end":140607906,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140607906,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799751678","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607907,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140607907,"seq_region_name":"7","id":"rs539380499","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799751916","clinical_significance":[],"end":140607910,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140607910,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140607914,"alleles":["T","C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607914,"clinical_significance":[],"seq_region_name":"7","id":"rs950339664"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799752157","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607917,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140607917},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799752261","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607918,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140607918},{"seq_region_name":"7","id":"rs987146228","clinical_significance":[],"start":140607920,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140607920,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607924,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140607924,"clinical_significance":[],"id":"rs558028673","seq_region_name":"7"},{"source":"dbSNP","start":140607926,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140607926,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799752589"},{"id":"rs767404961","seq_region_name":"7","clinical_significance":[],"start":140607927,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140607927,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs115773876","source":"dbSNP","start":140607928,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140607928,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs73500427","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140607932,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607932},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607938,"source":"dbSNP","strand":1,"feature_type":"variation","end":140607938,"alleles":["C","T"],"seq_region_name":"7","id":"rs1488968447","clinical_significance":[]},{"end":140607939,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140607939,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs562166879","clinical_significance":[]},{"seq_region_name":"7","id":"rs1215751189","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607944,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140607944},{"seq_region_name":"7","id":"rs574150541","clinical_significance":[],"start":140607945,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140607945,"alleles":["G","A","C"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607952,"source":"dbSNP","strand":1,"feature_type":"variation","end":140607952,"alleles":["C","A"],"seq_region_name":"7","id":"rs777246268","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1666106753","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140607956,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607956},{"seq_region_name":"7","id":"rs1799753564","clinical_significance":[],"start":140607962,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140607962,"strand":1,"feature_type":"variation"},{"start":140607966,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140607966,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130698385","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140607968,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607968,"clinical_significance":[],"seq_region_name":"7","id":"rs1380825169"},{"id":"rs1799753750","seq_region_name":"7","clinical_significance":[],"alleles":["A","G"],"end":140607974,"strand":1,"feature_type":"variation","start":140607974,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607975,"source":"dbSNP","strand":1,"feature_type":"variation","end":140607975,"alleles":["T","C"],"seq_region_name":"7","id":"rs116548109","clinical_significance":[]},{"clinical_significance":[],"id":"rs1311620363","seq_region_name":"7","alleles":["C","T"],"end":140607976,"feature_type":"variation","strand":1,"source":"dbSNP","start":140607976,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140607982,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140607982,"alleles":["T","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799754098","clinical_significance":[]},{"source":"dbSNP","start":140607988,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140607988,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1014455091"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607989,"source":"dbSNP","strand":1,"feature_type":"variation","end":140607989,"alleles":["C","A","G","T"],"id":"rs1025127915","seq_region_name":"7","clinical_significance":[]},{"alleles":["CCCCCC","CCCCC"],"end":140607994,"feature_type":"variation","strand":1,"source":"dbSNP","start":140607989,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1563175593"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140607990,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140607990,"clinical_significance":[],"id":"rs1298145347","seq_region_name":"7"},{"alleles":["C","T"],"end":140607992,"feature_type":"variation","strand":1,"source":"dbSNP","start":140607992,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799754753"},{"source":"dbSNP","start":140607993,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140607993,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799754859","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799754970","clinical_significance":[],"alleles":["C","G"],"end":140607994,"strand":1,"feature_type":"variation","start":140607994,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1799755065","seq_region_name":"7","clinical_significance":[],"end":140607995,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140607995,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1361272137","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140607998,"source":"dbSNP","strand":1,"feature_type":"variation","end":140608000,"alleles":["CCC","CCCC"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608006,"feature_type":"variation","strand":1,"end":140608006,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1174469066"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608010,"feature_type":"variation","strand":1,"end":140608010,"alleles":["C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799755393"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799755493","feature_type":"variation","strand":1,"end":140608016,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608016},{"clinical_significance":[],"id":"rs1799755588","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608020,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140608020},{"clinical_significance":[],"seq_region_name":"7","id":"rs1414254850","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608021,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140608021},{"seq_region_name":"7","id":"rs1799755797","clinical_significance":[],"alleles":["T","A"],"end":140608025,"strand":1,"feature_type":"variation","start":140608025,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs190774432","source":"dbSNP","start":140608028,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140608028,"feature_type":"variation","strand":1},{"start":140608031,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140608031,"alleles":["G","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs945346807","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140608034,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608034,"clinical_significance":[],"id":"rs1170916174","seq_region_name":"7"},{"seq_region_name":"7","id":"rs2130698492","clinical_significance":[],"start":140608035,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140608035,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"start":140608037,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140608037,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799756266","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608042,"source":"dbSNP","strand":1,"feature_type":"variation","end":140608042,"alleles":["T","C"],"seq_region_name":"7","id":"rs1046383475","clinical_significance":[]},{"seq_region_name":"7","id":"rs1563175621","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140608046,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608046,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608047,"feature_type":"variation","strand":1,"end":140608047,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1002251516"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585746802","source":"dbSNP","start":140608048,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140608048,"alleles":["A","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1420779029","clinical_significance":[],"alleles":["G","T"],"end":140608051,"strand":1,"feature_type":"variation","start":140608051,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799756921","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608052,"feature_type":"variation","strand":1,"end":140608051,"alleles":["-","AAA"]},{"feature_type":"variation","strand":1,"end":140608052,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608052,"clinical_significance":[],"seq_region_name":"7","id":"rs1799757033"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585746823","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608053,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140608053},{"start":140608057,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140608057,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1192866279","clinical_significance":[]},{"id":"rs1483505365","seq_region_name":"7","clinical_significance":[],"alleles":["A","G"],"end":140608058,"strand":1,"feature_type":"variation","start":140608058,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs927993147","seq_region_name":"7","end":140608059,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140608059,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140608060,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140608060,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs533336253","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608062,"source":"dbSNP","strand":1,"feature_type":"variation","end":140608062,"alleles":["C","T"],"seq_region_name":"7","id":"rs1204454724","clinical_significance":[]},{"clinical_significance":[],"id":"rs952394451","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608063,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140608063},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799758007","source":"dbSNP","start":140608064,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140608064,"feature_type":"variation","strand":1},{"end":140608070,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140608070,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs73500429","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608071,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140608071,"clinical_significance":[],"seq_region_name":"7","id":"rs1055812202"},{"seq_region_name":"7","id":"rs1799758362","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608074,"source":"dbSNP","strand":1,"feature_type":"variation","end":140608074,"alleles":["T","C"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608084,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140608084,"id":"rs1015546956","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1228948449","clinical_significance":[],"start":140608088,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140608088,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799758806","alleles":["A","T"],"end":140608101,"feature_type":"variation","strand":1,"source":"dbSNP","start":140608101,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799758958","source":"dbSNP","start":140608103,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140608103,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140608107,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608107,"clinical_significance":[],"seq_region_name":"7","id":"rs1382047549"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1301570320","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608108,"feature_type":"variation","strand":1,"end":140608108,"alleles":["A","G"]},{"start":140608109,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140608109,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1447819912","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140608121,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608121,"clinical_significance":[],"seq_region_name":"7","id":"rs1799759332"},{"id":"rs961483772","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140608123,"strand":1,"feature_type":"variation","start":140608123,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1401416502","clinical_significance":[],"strand":1,"feature_type":"variation","end":140608129,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608129,"source":"dbSNP"},{"end":140608130,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140608130,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs899313556"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608133,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140608133,"seq_region_name":"7","id":"rs1799759697","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608135,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140608135,"seq_region_name":"7","id":"rs1331648827","clinical_significance":[]},{"end":140608137,"alleles":["T","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140608137,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs995021931"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608137,"feature_type":"variation","strand":1,"alleles":["TACTTAAGTGAACTCACT","T"],"end":140608154,"clinical_significance":[],"seq_region_name":"7","id":"rs909563757"},{"clinical_significance":[],"id":"rs1169209557","seq_region_name":"7","end":140608138,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140608138,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130698652","feature_type":"variation","strand":1,"end":140608140,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608140},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608151,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140608151,"seq_region_name":"7","id":"rs1428888818","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1047483141","source":"dbSNP","start":140608155,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140608155,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1799760410","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608156,"feature_type":"variation","strand":1,"end":140608156,"alleles":["C","A"]},{"strand":1,"feature_type":"variation","alleles":["CCC","CC"],"end":140608158,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608156,"source":"dbSNP","seq_region_name":"7","id":"rs1585746999","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140608157,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608157,"source":"dbSNP","seq_region_name":"7","id":"rs2130698673","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608161,"feature_type":"variation","strand":1,"end":140608161,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs373811154"},{"seq_region_name":"7","id":"rs932760346","clinical_significance":[],"strand":1,"feature_type":"variation","end":140608162,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608162,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608163,"source":"dbSNP","strand":1,"feature_type":"variation","end":140608165,"alleles":["GGG","GG"],"seq_region_name":"7","id":"rs1799760810","clinical_significance":[]},{"seq_region_name":"7","id":"rs886196072","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608167,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140608167},{"id":"rs1799761026","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140608168,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608168,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608181,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140608181,"seq_region_name":"7","id":"rs1799761139","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799761231","clinical_significance":[],"alleles":["T","C"],"end":140608183,"strand":1,"feature_type":"variation","start":140608183,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1799761324","clinical_significance":[],"start":140608191,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140608191,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1472356901","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608192,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140608192},{"start":140608193,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140608193,"alleles":["G","C"],"strand":1,"feature_type":"variation","id":"rs1238518697","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","A","T"],"end":140608201,"feature_type":"variation","strand":1,"source":"dbSNP","start":140608201,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799761633","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608208,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140608208,"seq_region_name":"7","id":"rs1170255874","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1388182402","end":140608209,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140608209,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140608216,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140608220,"alleles":["CCATA","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs200413009"},{"strand":1,"feature_type":"variation","end":140608219,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608219,"source":"dbSNP","seq_region_name":"7","id":"rs1200772142","clinical_significance":[]},{"end":140608222,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140608222,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1799762180","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1008691591","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140608224,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608224},{"id":"rs1799762363","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608225,"source":"dbSNP","strand":1,"feature_type":"variation","end":140608225,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1799762477","clinical_significance":[],"end":140608227,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140608227,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1585747081","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608228,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140608228},{"seq_region_name":"7","id":"rs985388178","clinical_significance":[],"start":140608230,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140608230,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1799762775","clinical_significance":[],"start":140608234,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140608234,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"alleles":["T","C","G"],"end":140608235,"feature_type":"variation","strand":1,"source":"dbSNP","start":140608235,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs925954693"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608241,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140608241,"clinical_significance":[],"seq_region_name":"7","id":"rs1799763021"},{"clinical_significance":[],"id":"rs1799763124","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140608259,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608259},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799763231","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608262,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140608262},{"clinical_significance":[],"id":"rs1799763319","seq_region_name":"7","source":"dbSNP","start":140608263,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140608263,"alleles":["G","A"],"feature_type":"variation","strand":1},{"id":"rs1222452395","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608263,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GGGGG","GGGGGG"],"end":140608267},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140608264,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608264,"clinical_significance":[],"id":"rs1585747124","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799763612","end":140608267,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140608267,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1585747139","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140608268,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608268,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608270,"source":"dbSNP","strand":1,"feature_type":"variation","end":140608270,"alleles":["T","C"],"id":"rs1018605925","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608275,"source":"dbSNP","strand":1,"feature_type":"variation","end":140608280,"alleles":["CCCCCC","CCCCC","CCCCCCC"],"id":"rs1311231146","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1378111141","clinical_significance":[],"end":140608276,"alleles":["C","A","G"],"strand":1,"feature_type":"variation","start":140608276,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608277,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140608277,"clinical_significance":[],"seq_region_name":"7","id":"rs567751325"},{"source":"dbSNP","start":140608281,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140608281,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799764301","seq_region_name":"7"},{"clinical_significance":[],"id":"rs183017087","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608282,"feature_type":"variation","strand":1,"end":140608282,"alleles":["G","A","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799764517","source":"dbSNP","start":140608283,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140608284,"alleles":["AA","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1445015293","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608287,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140608287},{"source":"dbSNP","start":140608289,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140608289,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799764722","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608290,"feature_type":"variation","strand":1,"end":140608290,"alleles":["A","C"],"clinical_significance":[],"id":"rs1397759404","seq_region_name":"7"},{"start":140608295,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140608295,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1696919189","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140608296,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608296,"clinical_significance":[],"seq_region_name":"7","id":"rs1799764912"},{"source":"dbSNP","start":140608298,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140608298,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs538477184"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608300,"source":"dbSNP","strand":1,"feature_type":"variation","end":140608300,"alleles":["C","T"],"seq_region_name":"7","id":"rs1799765129","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799765234","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608301,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140608301},{"seq_region_name":"7","id":"rs1799765353","clinical_significance":[],"alleles":["A","G"],"end":140608302,"strand":1,"feature_type":"variation","start":140608302,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1297221910","clinical_significance":[],"strand":1,"feature_type":"variation","end":140608303,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608303,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608304,"source":"dbSNP","strand":1,"feature_type":"variation","end":140608304,"alleles":["C","A"],"seq_region_name":"7","id":"rs62485841","clinical_significance":[]},{"alleles":["T","C"],"end":140608311,"feature_type":"variation","strand":1,"source":"dbSNP","start":140608311,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799765678","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608318,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140608318,"clinical_significance":[],"id":"rs760181259","seq_region_name":"7"},{"start":140608321,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","T"],"end":140608321,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1053288043","clinical_significance":[]},{"clinical_significance":[],"id":"rs531018160","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608322,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140608322},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608322,"feature_type":"variation","strand":1,"end":140608324,"alleles":["AAA","A"],"clinical_significance":[],"id":"rs1799766101","seq_region_name":"7"},{"clinical_significance":[],"id":"rs950242731","seq_region_name":"7","source":"dbSNP","start":140608325,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140608325,"feature_type":"variation","strand":1},{"start":140608326,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","-"],"end":140608326,"strand":1,"feature_type":"variation","id":"rs375303265","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140608326,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608326,"source":"dbSNP","seq_region_name":"7","id":"rs756691630","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140608327,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608327,"clinical_significance":[],"seq_region_name":"7","id":"rs1799766538"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799766621","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608328,"feature_type":"variation","strand":1,"end":140608328,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799766728","feature_type":"variation","strand":1,"end":140608330,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608330},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608333,"source":"dbSNP","strand":1,"feature_type":"variation","end":140608333,"alleles":["A","C"],"seq_region_name":"7","id":"rs1799766849","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608336,"source":"dbSNP","strand":1,"feature_type":"variation","end":140608336,"alleles":["T","C"],"seq_region_name":"7","id":"rs1180347083","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608337,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140608337,"seq_region_name":"7","id":"rs1563175744","clinical_significance":[]},{"source":"dbSNP","start":140608339,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140608339,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799767162","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1362306434","source":"dbSNP","start":140608345,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140608345,"alleles":["A","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1437555820","end":140608346,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140608346,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs28694175","source":"dbSNP","start":140608351,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140608351,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140608366,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608366,"source":"dbSNP","id":"rs1300285923","seq_region_name":"7","clinical_significance":[]},{"start":140608367,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140608367,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs151104097","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608369,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140608369,"clinical_significance":[],"seq_region_name":"7","id":"rs1799767678"},{"seq_region_name":"7","id":"rs1489522491","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608371,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","-"],"end":140608371},{"id":"rs957175137","seq_region_name":"7","clinical_significance":[],"start":140608373,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140608373,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs2130699005","clinical_significance":[],"end":140608380,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140608380,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1799768038","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140608381,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608381,"source":"dbSNP"},{"alleles":["G","A"],"end":140608382,"strand":1,"feature_type":"variation","start":140608382,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799768139","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140608384,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608384,"source":"dbSNP","seq_region_name":"7","id":"rs2130699024","clinical_significance":[]},{"seq_region_name":"7","id":"rs1221488184","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608387,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140608387},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140608388,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608388,"clinical_significance":[],"seq_region_name":"7","id":"rs988614298"},{"start":140608394,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A","C","G"],"end":140608394,"strand":1,"feature_type":"variation","id":"rs913950698","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799769358","seq_region_name":"7","alleles":["A","G"],"end":140608403,"feature_type":"variation","strand":1,"source":"dbSNP","start":140608403,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608405,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140608405,"seq_region_name":"7","id":"rs1799769473","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140608409,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608409,"clinical_significance":[],"seq_region_name":"7","id":"rs1427256555"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799769669","alleles":["C","G"],"end":140608410,"feature_type":"variation","strand":1,"source":"dbSNP","start":140608410,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1305880959","alleles":["C","T"],"end":140608412,"feature_type":"variation","strand":1,"source":"dbSNP","start":140608412,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1585747407","clinical_significance":[],"end":140608415,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140608415,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608416,"feature_type":"variation","strand":1,"end":140608416,"alleles":["C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1386951808"},{"id":"rs576643170","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140608417,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608417,"source":"dbSNP"},{"alleles":["G","A"],"end":140608419,"feature_type":"variation","strand":1,"source":"dbSNP","start":140608419,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799770189"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140608423,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608423,"clinical_significance":[],"seq_region_name":"7","id":"rs1369108420"},{"clinical_significance":[],"id":"rs1412257425","seq_region_name":"7","feature_type":"variation","strand":1,"end":140608425,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608425},{"strand":1,"feature_type":"variation","end":140608431,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608431,"source":"dbSNP","id":"rs746361740","seq_region_name":"7","clinical_significance":[]},{"start":140608432,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140608432,"alleles":["T","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799770683","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799770797","clinical_significance":[],"alleles":["T","C"],"end":140608434,"strand":1,"feature_type":"variation","start":140608434,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1799770907","clinical_significance":[],"end":140608435,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140608435,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs982193624","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608438,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140608438},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140608442,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608442,"clinical_significance":[],"seq_region_name":"7","id":"rs772635651"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608443,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140608443,"seq_region_name":"7","id":"rs556273670","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608443,"feature_type":"variation","strand":1,"alleles":["GGGG","GGG"],"end":140608446,"clinical_significance":[],"seq_region_name":"7","id":"rs1361133837"},{"feature_type":"variation","strand":1,"end":140608444,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608444,"clinical_significance":[],"seq_region_name":"7","id":"rs1585747473"},{"id":"rs1799771575","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608445,"source":"dbSNP","strand":1,"feature_type":"variation","end":140608445,"alleles":["G","C"]},{"end":140608446,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140608446,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1563175821"},{"end":140608447,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140608447,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1585747495","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608449,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140608449,"clinical_significance":[],"id":"rs938031804","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140608450,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608450,"source":"dbSNP","seq_region_name":"7","id":"rs1799772003","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608453,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140608453,"clinical_significance":[],"seq_region_name":"7","id":"rs1055358319"},{"id":"rs1177058351","seq_region_name":"7","clinical_significance":[],"start":140608460,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140608460,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs528990123","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140608464,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608464,"source":"dbSNP"},{"end":140608466,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140608466,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799772345","clinical_significance":[]},{"id":"rs1265525231","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140608468,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608468,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1198879393","clinical_significance":[],"strand":1,"feature_type":"variation","end":140608469,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608469,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608470,"source":"dbSNP","strand":1,"feature_type":"variation","end":140608470,"alleles":["G","A"],"seq_region_name":"7","id":"rs547069416","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140608471,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608471,"source":"dbSNP","seq_region_name":"7","id":"rs930763840","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608483,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140608483,"clinical_significance":[],"seq_region_name":"7","id":"rs1488641991"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799772935","source":"dbSNP","start":140608484,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140608484,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs780435530","seq_region_name":"7","alleles":["A","G"],"end":140608490,"feature_type":"variation","strand":1,"source":"dbSNP","start":140608490,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1799773236","seq_region_name":"7","source":"dbSNP","start":140608493,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140608493,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608494,"source":"dbSNP","strand":1,"feature_type":"variation","end":140608494,"alleles":["T","C","G"],"seq_region_name":"7","id":"rs1005244799","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799773503","source":"dbSNP","start":140608496,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140608496,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1799773623","clinical_significance":[],"start":140608502,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140608502,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1353478563","seq_region_name":"7","source":"dbSNP","start":140608503,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140608503,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1799773806","clinical_significance":[],"alleles":["ATCG","ATCGATCG"],"end":140608506,"strand":1,"feature_type":"variation","start":140608503,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1799773912","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608504,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140608504},{"id":"rs1322925647","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608506,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140608506},{"end":140608508,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140608508,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1233538933","clinical_significance":[]},{"start":140608512,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140608512,"alleles":["A","G"],"strand":1,"feature_type":"variation","id":"rs1799774202","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","G"],"end":140608530,"strand":1,"feature_type":"variation","start":140608530,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1363436581","clinical_significance":[]},{"seq_region_name":"7","id":"rs886642415","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608532,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140608532},{"alleles":["G","A"],"end":140608533,"feature_type":"variation","strand":1,"source":"dbSNP","start":140608533,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1298698466"},{"seq_region_name":"7","id":"rs1799774692","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140608534,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608534,"source":"dbSNP"},{"end":140608535,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140608535,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1008638909"},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140608537,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608537,"source":"dbSNP","id":"rs1585747657","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799774992","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140608542,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608542},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799775111","source":"dbSNP","start":140608544,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140608544,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1799775218","clinical_significance":[],"start":140608548,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140608548,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1403850822","seq_region_name":"7","end":140608553,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140608553,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140608554,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140608554,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799775404","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140608558,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608558,"clinical_significance":[],"seq_region_name":"7","id":"rs1340543278"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608568,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140608568,"seq_region_name":"7","id":"rs747383800","clinical_significance":[]},{"seq_region_name":"7","id":"rs1397994439","clinical_significance":[],"end":140608569,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140608569,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["G","A"],"end":140608570,"strand":1,"feature_type":"variation","start":140608570,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1040550499","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs769086280","source":"dbSNP","start":140608571,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140608571,"alleles":["G","A","T"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140608574,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608574,"source":"dbSNP","seq_region_name":"7","id":"rs141103109","clinical_significance":[]},{"id":"rs1799776174","seq_region_name":"7","clinical_significance":[],"start":140608579,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140608579,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140608582,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608582,"clinical_significance":[],"seq_region_name":"7","id":"rs1799776264"},{"start":140608583,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140608583,"strand":1,"feature_type":"variation","id":"rs1799776349","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140608586,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140608586,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs996260259","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1799776514","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608589,"feature_type":"variation","strand":1,"end":140608589,"alleles":["T","C"]},{"strand":1,"feature_type":"variation","end":140608591,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608591,"source":"dbSNP","seq_region_name":"7","id":"rs1376178440","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140608595,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608595,"clinical_significance":[],"seq_region_name":"7","id":"rs1799776708"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563175894","end":140608597,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140608597,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140608599,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140608599,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799776886","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608600,"feature_type":"variation","strand":1,"alleles":["CAGCAG","CAG"],"end":140608605,"clinical_significance":[],"seq_region_name":"7","id":"rs1799776986"},{"feature_type":"variation","strand":1,"end":140608601,"alleles":["A","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608601,"clinical_significance":[],"seq_region_name":"7","id":"rs976957549"},{"id":"rs1478203291","seq_region_name":"7","clinical_significance":[],"start":140608601,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140608601,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799777265","source":"dbSNP","start":140608604,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140608604,"feature_type":"variation","strand":1},{"alleles":["G","A"],"end":140608608,"feature_type":"variation","strand":1,"source":"dbSNP","start":140608608,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1029501132"},{"clinical_significance":[],"seq_region_name":"7","id":"rs539408579","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608611,"feature_type":"variation","strand":1,"end":140608611,"alleles":["G","A"]},{"source":"dbSNP","start":140608613,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140608613,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1192133828","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1217486535","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608614,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140608614},{"clinical_significance":[],"seq_region_name":"7","id":"rs557775100","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140608618,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608618},{"source":"dbSNP","start":140608620,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140608620,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs957289057"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608623,"source":"dbSNP","strand":1,"feature_type":"variation","end":140608623,"alleles":["C","G"],"seq_region_name":"7","id":"rs1202593201","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1482467361","source":"dbSNP","start":140608625,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140608625,"alleles":["G","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1260889343","clinical_significance":[],"start":140608626,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140608626,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608627,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140608627,"id":"rs1010145888","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608629,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140608629,"seq_region_name":"7","id":"rs1799778463","clinical_significance":[]},{"seq_region_name":"7","id":"rs7789961","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608632,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140608632},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140608633,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608633,"clinical_significance":[],"seq_region_name":"7","id":"rs1318002978"},{"clinical_significance":[],"id":"rs577837134","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608634,"feature_type":"variation","strand":1,"end":140608634,"alleles":["C","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608639,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140608639,"clinical_significance":[],"seq_region_name":"7","id":"rs1799778941"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608645,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140608645,"seq_region_name":"7","id":"rs1210789387","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs982198011","source":"dbSNP","start":140608647,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140608647,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140608649,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140608652,"alleles":["CCAG","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799779235"},{"seq_region_name":"7","id":"rs1325856767","clinical_significance":[],"start":140608652,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140608652,"strand":1,"feature_type":"variation"},{"id":"rs187111677","seq_region_name":"7","clinical_significance":[],"start":140608653,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C","T"],"end":140608653,"strand":1,"feature_type":"variation"},{"id":"rs1799779523","seq_region_name":"7","clinical_significance":[],"end":140608655,"alleles":["-","GATA"],"strand":1,"feature_type":"variation","start":140608656,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["C","T"],"end":140608657,"strand":1,"feature_type":"variation","start":140608657,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799779611","clinical_significance":[]},{"seq_region_name":"7","id":"rs1399736508","clinical_significance":[],"start":140608659,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140608659,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608666,"source":"dbSNP","strand":1,"feature_type":"variation","end":140608666,"alleles":["A","G","T"],"seq_region_name":"7","id":"rs913448586","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585747909","clinical_significance":[],"strand":1,"feature_type":"variation","end":140608668,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608668,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1464263783","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140608669,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608669,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608673,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140608673,"id":"rs1799780108","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608675,"feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140608675,"clinical_significance":[],"seq_region_name":"7","id":"rs1799780205"},{"strand":1,"feature_type":"variation","alleles":["TA","-"],"end":140608676,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608675,"source":"dbSNP","id":"rs1799780311","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140608676,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608676,"source":"dbSNP","id":"rs1422466544","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140608676,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140608692,"alleles":["AAAAAAAAAAAAAAAAA","AAAAAAAAAAAAA","AAAAAAAAAAAAAA","AAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs11358052"},{"seq_region_name":"7","id":"rs1799780837","clinical_significance":[],"alleles":["A","G","T"],"end":140608677,"strand":1,"feature_type":"variation","start":140608677,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140608679,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140608679,"strand":1,"feature_type":"variation","id":"rs1585747952","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130699568","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140608682,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608682,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140608685,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608685,"source":"dbSNP","seq_region_name":"7","id":"rs1799781061","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608690,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140608690,"clinical_significance":[],"seq_region_name":"7","id":"rs1799781150"},{"seq_region_name":"7","id":"rs1799781230","clinical_significance":[],"strand":1,"feature_type":"variation","end":140608693,"alleles":["AAT","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608691,"source":"dbSNP"},{"seq_region_name":"7","id":"rs928056933","clinical_significance":[],"alleles":["A","G","T"],"end":140608692,"strand":1,"feature_type":"variation","start":140608692,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140608693,"alleles":["T","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140608693,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs950340145"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608693,"feature_type":"variation","strand":1,"alleles":["T","-"],"end":140608693,"clinical_significance":[],"id":"rs1199392672","seq_region_name":"7"},{"end":140608694,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140608694,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1259580700"},{"seq_region_name":"7","id":"rs1046440468","clinical_significance":[],"end":140608703,"alleles":["ATTAATTAA","ATTAA"],"strand":1,"feature_type":"variation","start":140608695,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140608697,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608697,"source":"dbSNP","seq_region_name":"7","id":"rs1799781795","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140608700,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608700,"clinical_significance":[],"seq_region_name":"7","id":"rs959372273"},{"clinical_significance":[],"seq_region_name":"7","id":"rs927473936","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608702,"feature_type":"variation","strand":1,"end":140608702,"alleles":["A","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585748018","feature_type":"variation","strand":1,"end":140608705,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608705},{"seq_region_name":"7","id":"rs1799782158","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608706,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140608706},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140608708,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608708,"clinical_significance":[],"seq_region_name":"7","id":"rs868775498"},{"start":140608709,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C"],"end":140608709,"strand":1,"feature_type":"variation","id":"rs1799782361","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585748029","alleles":["A","C","T"],"end":140608711,"feature_type":"variation","strand":1,"source":"dbSNP","start":140608711,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140608713,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608713,"clinical_significance":[],"seq_region_name":"7","id":"rs1585748039"},{"seq_region_name":"7","id":"rs920816603","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608718,"source":"dbSNP","strand":1,"feature_type":"variation","end":140608718,"alleles":["C","T"]},{"source":"dbSNP","start":140608719,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140608719,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs930874658"},{"strand":1,"feature_type":"variation","end":140608721,"alleles":["AA","AAA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608720,"source":"dbSNP","id":"rs1799782879","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140608721,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140608721,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1338493303"},{"seq_region_name":"7","id":"rs1314035579","clinical_significance":[],"alleles":["T","C"],"end":140608730,"strand":1,"feature_type":"variation","start":140608730,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1447229758","feature_type":"variation","strand":1,"end":140608734,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608734},{"clinical_significance":[],"seq_region_name":"7","id":"rs1379446324","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608735,"feature_type":"variation","strand":1,"end":140608735,"alleles":["A","G"]},{"source":"dbSNP","start":140608738,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140608738,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs983733360"},{"seq_region_name":"7","id":"rs574772025","clinical_significance":[],"strand":1,"feature_type":"variation","end":140608746,"alleles":["A","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608746,"source":"dbSNP"},{"id":"rs1165510634","seq_region_name":"7","clinical_significance":[],"start":140608750,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140608750,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"start":140608752,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140608752,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs944875479","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1156482462","feature_type":"variation","strand":1,"end":140608756,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608756},{"strand":1,"feature_type":"variation","end":140608759,"alleles":["T","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608759,"source":"dbSNP","seq_region_name":"7","id":"rs1040096420","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs900259563","source":"dbSNP","start":140608760,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140608760,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140608766,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608766,"clinical_significance":[],"seq_region_name":"7","id":"rs1441899920"},{"clinical_significance":[],"seq_region_name":"7","id":"rs573861800","source":"dbSNP","start":140608769,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140608769,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1054528147","clinical_significance":[],"end":140608770,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140608770,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1179168281","clinical_significance":[],"strand":1,"feature_type":"variation","end":140608771,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608771,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1799784347","seq_region_name":"7","end":140608775,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140608775,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs892835667","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608778,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140608778},{"seq_region_name":"7","id":"rs541563598","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140608781,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608781,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1010093000","end":140608783,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140608783,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799784707","source":"dbSNP","start":140608786,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140608786,"alleles":["C","T"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608792,"feature_type":"variation","strand":1,"end":140608792,"alleles":["T","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799784794"},{"clinical_significance":[],"id":"rs1436757422","seq_region_name":"7","source":"dbSNP","start":140608793,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140608793,"alleles":["T","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1799784974","clinical_significance":[],"start":140608802,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140608802,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs897024863","clinical_significance":[],"end":140608805,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140608805,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1020180228","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140608814,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608814,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608821,"feature_type":"variation","strand":1,"end":140608821,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585748247"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1211582667","feature_type":"variation","strand":1,"end":140608822,"alleles":["G","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608822},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140608825,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608825,"clinical_significance":[],"seq_region_name":"7","id":"rs2130699817"},{"feature_type":"variation","strand":1,"end":140608827,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608827,"clinical_significance":[],"seq_region_name":"7","id":"rs1799785414"},{"alleles":["G","A"],"end":140608829,"feature_type":"variation","strand":1,"source":"dbSNP","start":140608829,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799785513"},{"seq_region_name":"7","id":"rs907019707","clinical_significance":[],"strand":1,"feature_type":"variation","end":140608830,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608830,"source":"dbSNP"},{"start":140608832,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140608832,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799785704","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608834,"source":"dbSNP","strand":1,"feature_type":"variation","end":140608834,"alleles":["T","G"],"seq_region_name":"7","id":"rs1290942631","clinical_significance":[]},{"id":"rs1324627949","seq_region_name":"7","clinical_significance":[],"end":140608837,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140608837,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140608841,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608841,"source":"dbSNP","seq_region_name":"7","id":"rs553427331","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799786072","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608845,"feature_type":"variation","strand":1,"end":140608845,"alleles":["C","G"]},{"clinical_significance":[],"id":"rs1799786153","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608848,"feature_type":"variation","strand":1,"end":140608848,"alleles":["C","G","T"]},{"seq_region_name":"7","id":"rs577968789","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608851,"source":"dbSNP","strand":1,"feature_type":"variation","end":140608851,"alleles":["G","A"]},{"feature_type":"variation","strand":1,"end":140608853,"alleles":["G","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608853,"clinical_significance":[],"seq_region_name":"7","id":"rs998110989"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140608857,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608857,"source":"dbSNP","seq_region_name":"7","id":"rs1799786462","clinical_significance":[]},{"seq_region_name":"7","id":"rs1278032889","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140608859,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608859,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1333283956","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608863,"feature_type":"variation","strand":1,"end":140608863,"alleles":["A","T"]},{"seq_region_name":"7","id":"rs1441661278","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608868,"source":"dbSNP","strand":1,"feature_type":"variation","end":140608868,"alleles":["T","C"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608869,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140608869,"clinical_significance":[],"seq_region_name":"7","id":"rs1799786817"},{"start":140608879,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140608881,"alleles":["GGG","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs773296532","clinical_significance":[]},{"alleles":["C","T"],"end":140608882,"strand":1,"feature_type":"variation","start":140608882,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1434984260","clinical_significance":[]},{"source":"dbSNP","start":140608887,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140608887,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799787097"},{"strand":1,"feature_type":"variation","end":140608890,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608890,"source":"dbSNP","id":"rs190365776","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","A","C"],"end":140608891,"strand":1,"feature_type":"variation","start":140608891,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs563852485","clinical_significance":[]},{"start":140608892,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140608892,"alleles":["A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799787430","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140608899,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608899,"clinical_significance":[],"id":"rs182762563","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608902,"feature_type":"variation","strand":1,"end":140608902,"alleles":["A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs959723826"},{"end":140608903,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140608903,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs542898980","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs187374896","feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140608904,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608904},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608905,"source":"dbSNP","strand":1,"feature_type":"variation","end":140608905,"alleles":["T","C"],"seq_region_name":"7","id":"rs1328761690","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608907,"source":"dbSNP","strand":1,"feature_type":"variation","end":140608907,"alleles":["C","G"],"seq_region_name":"7","id":"rs1421932886","clinical_significance":[]},{"start":140608908,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140608908,"alleles":["C","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799788166","clinical_significance":[]},{"id":"rs1378815600","seq_region_name":"7","clinical_significance":[],"end":140608917,"alleles":["CCAAC","C"],"strand":1,"feature_type":"variation","start":140608913,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140608914,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140608914,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799788368","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585748427","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608916,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140608916},{"clinical_significance":[],"seq_region_name":"7","id":"rs528661104","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140608925,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608925},{"alleles":["C","G"],"end":140608928,"feature_type":"variation","strand":1,"source":"dbSNP","start":140608928,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1469258534"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140608938,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608938,"clinical_significance":[],"id":"rs1799788646","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140608939,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608939,"source":"dbSNP","seq_region_name":"7","id":"rs1246913747","clinical_significance":[]},{"id":"rs952050911","seq_region_name":"7","clinical_significance":[],"alleles":["C","G"],"end":140608940,"strand":1,"feature_type":"variation","start":140608940,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140608942,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140608942,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1554479980","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["TAAATAT","T"],"end":140608953,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608947,"clinical_significance":[],"seq_region_name":"7","id":"rs1489625209"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140608950,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608950,"source":"dbSNP","id":"rs983681085","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1210157151","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140608953,"feature_type":"variation","strand":1,"end":140608953,"alleles":["T","C","G"]},{"seq_region_name":"7","id":"rs1799789345","clinical_significance":[],"start":140608956,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140608956,"strand":1,"feature_type":"variation"},{"alleles":["A","G"],"end":140608964,"feature_type":"variation","strand":1,"source":"dbSNP","start":140608964,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs957467048"},{"clinical_significance":[],"id":"rs1281808549","seq_region_name":"7","source":"dbSNP","start":140608966,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140608966,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs76718739","alleles":["C","G","T"],"end":140608968,"feature_type":"variation","strand":1,"source":"dbSNP","start":140608968,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140608969,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140608969,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs145236837"},{"seq_region_name":"7","id":"rs1276794781","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140608970,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608970,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140608975,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608975,"source":"dbSNP","id":"rs1221819452","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140608979,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C","G"],"end":140608979,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1220703068"},{"end":140608980,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140608980,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1252517281","clinical_significance":[]},{"end":140608982,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140608982,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130700055"},{"seq_region_name":"7","id":"rs1799790342","clinical_significance":[],"alleles":["C","A"],"end":140608983,"strand":1,"feature_type":"variation","start":140608983,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1799790439","clinical_significance":[],"end":140608984,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140608984,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["C","T"],"end":140608988,"feature_type":"variation","strand":1,"source":"dbSNP","start":140608988,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs976661798","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799790613","clinical_significance":[],"strand":1,"feature_type":"variation","end":140608992,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140608992,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1799790728","seq_region_name":"7","source":"dbSNP","start":140608996,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140608996,"alleles":["T","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130700083","source":"dbSNP","start":140609001,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140609001,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs532791355","clinical_significance":[],"start":140609003,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","T"],"end":140609003,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609005,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140609005,"id":"rs971835978","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609006,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140609006,"id":"rs922164726","seq_region_name":"7","clinical_significance":[]},{"end":140609010,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140609010,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799791208"},{"end":140609013,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140609013,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1415399295","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799791377","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609015,"feature_type":"variation","strand":1,"end":140609015,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799791461","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609024,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140609024},{"seq_region_name":"7","id":"rs2130700130","clinical_significance":[],"end":140609028,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140609028,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["A","G"],"end":140609031,"feature_type":"variation","strand":1,"source":"dbSNP","start":140609031,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs931714944"},{"seq_region_name":"7","id":"rs1799791638","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609032,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140609032},{"clinical_significance":[],"seq_region_name":"7","id":"rs1425480986","feature_type":"variation","strand":1,"end":140609035,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609035},{"clinical_significance":[],"id":"rs981702419","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609036,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140609036},{"strand":1,"feature_type":"variation","alleles":["GAG","-"],"end":140609043,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609041,"source":"dbSNP","seq_region_name":"7","id":"rs2130700147","clinical_significance":[]},{"seq_region_name":"7","id":"rs1479188363","clinical_significance":[],"strand":1,"feature_type":"variation","end":140609042,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609042,"source":"dbSNP"},{"alleles":["A","G"],"end":140609049,"feature_type":"variation","strand":1,"source":"dbSNP","start":140609049,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1427907434"},{"strand":1,"feature_type":"variation","end":140609050,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609050,"source":"dbSNP","seq_region_name":"7","id":"rs551325668","clinical_significance":[]},{"end":140609051,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140609051,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1799792355","seq_region_name":"7","clinical_significance":[]},{"start":140609052,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140609052,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1410758916","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799792579","end":140609055,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140609055,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1240278736","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609059,"source":"dbSNP","strand":1,"feature_type":"variation","end":140609059,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1472952176","end":140609060,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140609060,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140609061,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609061,"clinical_significance":[],"seq_region_name":"7","id":"rs137909846"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1281028100","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140609072,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609072},{"start":140609073,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140609077,"alleles":["TTTTT","TTTT"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1201970622","clinical_significance":[]},{"alleles":["A","T"],"end":140609080,"strand":1,"feature_type":"variation","start":140609080,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs759538431","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585748792","clinical_significance":[],"start":140609083,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140609083,"strand":1,"feature_type":"variation"},{"id":"rs1278862946","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140609084,"strand":1,"feature_type":"variation","start":140609084,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs945733104","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140609087,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609087,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799793717","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609088,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140609088},{"strand":1,"feature_type":"variation","end":140609090,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609090,"source":"dbSNP","seq_region_name":"7","id":"rs1799793822","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140609092,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609092,"source":"dbSNP","seq_region_name":"7","id":"rs1220529276","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140609097,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609097,"clinical_significance":[],"seq_region_name":"7","id":"rs1360572206"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609101,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140609101,"seq_region_name":"7","id":"rs1393277781","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140609103,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609103,"source":"dbSNP","seq_region_name":"7","id":"rs1799794271","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609109,"source":"dbSNP","strand":1,"feature_type":"variation","end":140609109,"alleles":["A","T"],"seq_region_name":"7","id":"rs1799794382","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799794483","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609110,"source":"dbSNP","strand":1,"feature_type":"variation","end":140609110,"alleles":["T","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799794573","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609112,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140609112},{"seq_region_name":"7","id":"rs1449243011","clinical_significance":[],"start":140609120,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140609120,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140609121,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609121,"clinical_significance":[],"seq_region_name":"7","id":"rs1799794802"},{"start":140609124,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140609124,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799794909","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799795010","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609126,"source":"dbSNP","strand":1,"feature_type":"variation","end":140609126,"alleles":["A","G"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609127,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140609127,"clinical_significance":[],"seq_region_name":"7","id":"rs1799795126"},{"seq_region_name":"7","id":"rs937468073","clinical_significance":[],"strand":1,"feature_type":"variation","end":140609128,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609128,"source":"dbSNP"},{"alleles":["T","TT"],"end":140609130,"strand":1,"feature_type":"variation","start":140609130,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1338300200","clinical_significance":[]},{"end":140609131,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140609131,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1403977410","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799795567","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609143,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140609143},{"seq_region_name":"7","id":"rs1467849719","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609144,"source":"dbSNP","strand":1,"feature_type":"variation","end":140609144,"alleles":["A","G","T"]},{"strand":1,"feature_type":"variation","end":140609150,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609150,"source":"dbSNP","seq_region_name":"7","id":"rs537377229","clinical_significance":[]},{"source":"dbSNP","start":140609151,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140609151,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799795933"},{"seq_region_name":"7","id":"rs1478497826","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609160,"source":"dbSNP","strand":1,"feature_type":"variation","end":140609160,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1417353194","clinical_significance":[],"alleles":["A","T"],"end":140609164,"strand":1,"feature_type":"variation","start":140609164,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140609165,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140609165,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799796296","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799796391","clinical_significance":[],"strand":1,"feature_type":"variation","end":140609167,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609167,"source":"dbSNP"},{"id":"rs1799796503","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140609172,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609172,"source":"dbSNP"},{"id":"rs1799796613","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140609174,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609174,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1799796702","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140609175,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609175},{"seq_region_name":"7","id":"rs1049271440","clinical_significance":[],"start":140609181,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140609181,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1799796919","seq_region_name":"7","feature_type":"variation","strand":1,"end":140609190,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609190},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140609197,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609197,"clinical_significance":[],"seq_region_name":"7","id":"rs1323410566"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1473023383","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140609206,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609206},{"alleles":["T","C"],"end":140609207,"strand":1,"feature_type":"variation","start":140609207,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs909598720","clinical_significance":[]},{"end":140609212,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140609212,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799797344","clinical_significance":[]},{"seq_region_name":"7","id":"rs1202027822","clinical_significance":[],"start":140609218,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140609218,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799797546","source":"dbSNP","start":140609229,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140609229,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs140884688","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609230,"source":"dbSNP","strand":1,"feature_type":"variation","end":140609230,"alleles":["T","C"]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140609231,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609231,"source":"dbSNP","seq_region_name":"7","id":"rs1799797807","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs907135848","end":140609233,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140609233,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1286593104","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140609237,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609237,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609242,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140609242,"clinical_significance":[],"seq_region_name":"7","id":"rs542287174"},{"clinical_significance":[],"id":"rs1037228169","seq_region_name":"7","alleles":["G","A"],"end":140609244,"feature_type":"variation","strand":1,"source":"dbSNP","start":140609244,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs386718484","source":"dbSNP","start":140609244,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["GGC","ATT"],"end":140609246,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140609245,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140609245,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs896811219","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140609246,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609246,"clinical_significance":[],"seq_region_name":"7","id":"rs998288667"},{"end":140609248,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140609248,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799798634"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609255,"feature_type":"variation","strand":1,"end":140609255,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1227541483"},{"seq_region_name":"7","id":"rs1799798847","clinical_significance":[],"start":140609263,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140609263,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1585749027","seq_region_name":"7","source":"dbSNP","start":140609264,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140609264,"alleles":["G","C"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609266,"source":"dbSNP","strand":1,"feature_type":"variation","end":140609266,"alleles":["A","G"],"seq_region_name":"7","id":"rs1313448651","clinical_significance":[]},{"alleles":["C","A","G"],"end":140609267,"strand":1,"feature_type":"variation","start":140609267,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs767391560","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140609270,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609270,"source":"dbSNP","seq_region_name":"7","id":"rs1799799256","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609276,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140609276,"clinical_significance":[],"seq_region_name":"7","id":"rs1034593531"},{"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140609283,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609283,"clinical_significance":[],"seq_region_name":"7","id":"rs1275263251"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609284,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140609284,"seq_region_name":"7","id":"rs1331579704","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585749094","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609286,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140609286},{"seq_region_name":"7","id":"rs1484030838","clinical_significance":[],"start":140609287,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","G","T"],"end":140609287,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs894338584","seq_region_name":"7","feature_type":"variation","strand":1,"end":140609288,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609288},{"end":140609290,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140609290,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799800074"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799800193","source":"dbSNP","start":140609300,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140609300,"alleles":["G","T"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140609301,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140609301,"alleles":["T","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585749117"},{"alleles":["C","T"],"end":140609302,"strand":1,"feature_type":"variation","start":140609302,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1250484973","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1169665977","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609303,"feature_type":"variation","strand":1,"end":140609303,"alleles":["A","G"]},{"end":140609308,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140609308,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585749141"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1012727841","alleles":["C","A","G"],"end":140609315,"feature_type":"variation","strand":1,"source":"dbSNP","start":140609315,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1051004902","feature_type":"variation","strand":1,"alleles":["G","C","T"],"end":140609318,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609318},{"alleles":["G","C"],"end":140609322,"strand":1,"feature_type":"variation","start":140609322,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1027760300","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1189135369","end":140609324,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140609324,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1006651985","source":"dbSNP","start":140609328,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140609328,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609329,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140609329,"seq_region_name":"7","id":"rs1471976327","clinical_significance":[]},{"alleles":["T","C"],"end":140609330,"feature_type":"variation","strand":1,"source":"dbSNP","start":140609330,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs534771427","seq_region_name":"7"},{"id":"rs553195404","seq_region_name":"7","clinical_significance":[],"start":140609332,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140609332,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1799805958","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140609338,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609338,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609338,"source":"dbSNP","strand":1,"feature_type":"variation","end":140609340,"alleles":["CCC","CC"],"seq_region_name":"7","id":"rs563660218","clinical_significance":[]},{"source":"dbSNP","start":140609339,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","G"],"end":140609339,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs578024968"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799806523","end":140609343,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140609343,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1432224189","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609344,"source":"dbSNP","strand":1,"feature_type":"variation","end":140609344,"alleles":["C","T"]},{"source":"dbSNP","start":140609355,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140609355,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1306227677"},{"end":140609366,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140609366,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1799807005","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1222380950","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609372,"source":"dbSNP","strand":1,"feature_type":"variation","end":140609372,"alleles":["G","A"]},{"start":140609373,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140609373,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs192157376","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs575815685","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609374,"feature_type":"variation","strand":1,"end":140609374,"alleles":["G","A","C"]},{"clinical_significance":[],"id":"rs1010310668","seq_region_name":"7","source":"dbSNP","start":140609377,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140609377,"feature_type":"variation","strand":1},{"end":140609379,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140609379,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1354802119","clinical_significance":[]},{"start":140609383,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140609383,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1020814274","clinical_significance":[]},{"source":"dbSNP","start":140609385,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140609385,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1392707272"},{"alleles":["G","T"],"end":140609386,"feature_type":"variation","strand":1,"source":"dbSNP","start":140609386,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799808333","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1370563259","feature_type":"variation","strand":1,"end":140609387,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609387},{"seq_region_name":"7","id":"rs1297164449","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140609390,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609390,"source":"dbSNP"},{"source":"dbSNP","start":140609393,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140609393,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799808621","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1015146368","source":"dbSNP","start":140609394,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140609394,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1336334144","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140609395,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609395,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799809186","clinical_significance":[],"end":140609397,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140609397,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1367416308","alleles":["A","T"],"end":140609398,"feature_type":"variation","strand":1,"source":"dbSNP","start":140609398,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140609403,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609403,"clinical_significance":[],"seq_region_name":"7","id":"rs971402234"},{"strand":1,"feature_type":"variation","end":140609413,"alleles":["CTCGGGAGGCT","CT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609403,"source":"dbSNP","id":"rs1338928028","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140609404,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140609404,"alleles":["T","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799809776","seq_region_name":"7"},{"source":"dbSNP","start":140609405,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140609405,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs966695379"},{"end":140609406,"alleles":["G","A","C","T"],"strand":1,"feature_type":"variation","start":140609406,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs976397660","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609416,"feature_type":"variation","strand":1,"end":140609416,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799810331"},{"strand":1,"feature_type":"variation","end":140609426,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609426,"source":"dbSNP","seq_region_name":"7","id":"rs981866367","clinical_significance":[]},{"seq_region_name":"7","id":"rs922079060","clinical_significance":[],"strand":1,"feature_type":"variation","end":140609427,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609427,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs12667646","feature_type":"variation","strand":1,"end":140609428,"alleles":["G","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609428},{"strand":1,"feature_type":"variation","end":140609429,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609429,"source":"dbSNP","seq_region_name":"7","id":"rs1489490768","clinical_significance":[]},{"id":"rs1799811837","seq_region_name":"7","clinical_significance":[],"end":140609435,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140609435,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs989832974","clinical_significance":[],"alleles":["A","G"],"end":140609438,"strand":1,"feature_type":"variation","start":140609438,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609440,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140609440,"id":"rs1345038946","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609444,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140609444,"seq_region_name":"7","id":"rs914334286","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140609445,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609445,"clinical_significance":[],"seq_region_name":"7","id":"rs368330053"},{"seq_region_name":"7","id":"rs958951593","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609446,"source":"dbSNP","strand":1,"feature_type":"variation","end":140609446,"alleles":["G","A"]},{"clinical_significance":[],"id":"rs1799812750","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609447,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140609447},{"seq_region_name":"7","id":"rs1441546557","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609457,"source":"dbSNP","strand":1,"feature_type":"variation","end":140609457,"alleles":["A","G"]},{"end":140609459,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140609459,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799813104","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799813264","source":"dbSNP","start":140609461,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140609461,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs542962694","clinical_significance":[],"alleles":["G","A"],"end":140609462,"strand":1,"feature_type":"variation","start":140609462,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140609464,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140609464,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799813574"},{"seq_region_name":"7","id":"rs1305813839","clinical_significance":[],"alleles":["A","G"],"end":140609465,"strand":1,"feature_type":"variation","start":140609465,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs928359396","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140609467,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609467,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609468,"source":"dbSNP","strand":1,"feature_type":"variation","end":140609468,"alleles":["G","A","T"],"seq_region_name":"7","id":"rs1183344016","clinical_significance":[]},{"id":"rs984916779","seq_region_name":"7","clinical_significance":[],"start":140609470,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140609470,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs909376553","source":"dbSNP","start":140609471,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140609471,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799814441","end":140609481,"alleles":["TACTC","TACTCTACTC"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140609477,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1361074153","clinical_significance":[],"strand":1,"feature_type":"variation","end":140609478,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609478,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130700819","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609486,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140609486},{"alleles":["G","T"],"end":140609490,"feature_type":"variation","strand":1,"source":"dbSNP","start":140609490,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1290480967"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799814850","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609493,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140609493},{"start":140609496,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140609496,"strand":1,"feature_type":"variation","id":"rs938589304","seq_region_name":"7","clinical_significance":[]},{"id":"rs1799815116","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609499,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140609499},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140609502,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609502,"source":"dbSNP","seq_region_name":"7","id":"rs1363484690","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140609506,"alleles":["C","A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609506,"source":"dbSNP","seq_region_name":"7","id":"rs538601967","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140609507,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609507,"source":"dbSNP","seq_region_name":"7","id":"rs1799815433","clinical_significance":[]},{"start":140609507,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TTTTTT","TTTT","TTTTT"],"end":140609512,"strand":1,"feature_type":"variation","id":"rs376844663","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609513,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140609513,"clinical_significance":[],"seq_region_name":"7","id":"rs1176993383"},{"strand":1,"feature_type":"variation","end":140609515,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609515,"source":"dbSNP","seq_region_name":"7","id":"rs1799815942","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799816090","clinical_significance":[],"start":140609525,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140609525,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609529,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140609529,"id":"rs796147865","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799816390","clinical_significance":[],"start":140609531,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140609533,"alleles":["AAA","A"],"strand":1,"feature_type":"variation"},{"alleles":["AAAAAAAA","AAAAAA","AAAAAAA","AAAAAAAAA"],"end":140609542,"feature_type":"variation","strand":1,"source":"dbSNP","start":140609535,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs139162302","seq_region_name":"7"},{"end":140609538,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140609538,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1055739493","seq_region_name":"7"},{"alleles":["T","A"],"end":140609543,"strand":1,"feature_type":"variation","start":140609543,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs894276820","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs565435112","end":140609548,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140609548,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140609559,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609559,"source":"dbSNP","seq_region_name":"7","id":"rs1199348578","clinical_significance":[]},{"seq_region_name":"7","id":"rs1478470230","clinical_significance":[],"end":140609561,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140609561,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140609563,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140609563,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1264479388","clinical_significance":[]},{"alleles":["A","G"],"end":140609564,"feature_type":"variation","strand":1,"source":"dbSNP","start":140609564,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1203797733"},{"start":140609565,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140609565,"alleles":["C","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799817834","clinical_significance":[]},{"alleles":["T","C"],"end":140609573,"feature_type":"variation","strand":1,"source":"dbSNP","start":140609573,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1485733573"},{"source":"dbSNP","start":140609578,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140609578,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs972497246"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1325087584","source":"dbSNP","start":140609590,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140609590,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1280874581","seq_region_name":"7","source":"dbSNP","start":140609591,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140609595,"alleles":["ACACA","ACA"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1222370727","clinical_significance":[],"alleles":["C","T"],"end":140609592,"strand":1,"feature_type":"variation","start":140609592,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609593,"feature_type":"variation","strand":1,"end":140609593,"alleles":["A","C","G"],"clinical_significance":[],"id":"rs1373020682","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799819044","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609594,"source":"dbSNP","strand":1,"feature_type":"variation","end":140609594,"alleles":["C","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799819186","source":"dbSNP","start":140609595,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140609595,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140609597,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609597,"source":"dbSNP","seq_region_name":"7","id":"rs1466552814","clinical_significance":[]},{"end":140609598,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140609598,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1380331219"},{"clinical_significance":[],"id":"rs540771925","seq_region_name":"7","source":"dbSNP","start":140609601,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140609601,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1361732458","source":"dbSNP","start":140609601,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140609601,"alleles":["T","TGT"],"feature_type":"variation","strand":1},{"end":140609602,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140609602,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1238232971","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609603,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140609603,"id":"rs918356456","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609605,"source":"dbSNP","strand":1,"feature_type":"variation","end":140609605,"alleles":["A","G"],"seq_region_name":"7","id":"rs1400310913","clinical_significance":[]},{"clinical_significance":[],"id":"rs1471047151","seq_region_name":"7","source":"dbSNP","start":140609608,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TTTTTT","TTTTT","TTTTTTT"],"end":140609613,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs933649321","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140609610,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609610},{"clinical_significance":[],"seq_region_name":"7","id":"rs76922726","end":140609616,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140609616,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1799821040","clinical_significance":[],"strand":1,"feature_type":"variation","end":140609617,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609617,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140609618,"alleles":["GG","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609617,"clinical_significance":[],"seq_region_name":"7","id":"rs1799821211"},{"seq_region_name":"7","id":"rs1799821384","clinical_significance":[],"start":140609619,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140609619,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"start":140609620,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140609620,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1478173814","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1049143342","source":"dbSNP","start":140609624,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140609624,"alleles":["A","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1375336418","source":"dbSNP","start":140609627,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140609627,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs533007721","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609630,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140609630},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799822223","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140609636,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609636},{"id":"rs1428326851","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140609641,"alleles":["A","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609641,"source":"dbSNP"},{"end":140609644,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140609644,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799822585","clinical_significance":[]},{"seq_region_name":"7","id":"rs889667659","clinical_significance":[],"alleles":["C","T"],"end":140609646,"strand":1,"feature_type":"variation","start":140609646,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140609655,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609655,"clinical_significance":[],"seq_region_name":"7","id":"rs551173369"},{"source":"dbSNP","start":140609656,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140609656,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1296697300"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799823038","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140609662,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609662},{"source":"dbSNP","start":140609665,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140609665,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799823146"},{"id":"rs1005012406","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609670,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140609670},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799823324","feature_type":"variation","strand":1,"end":140609684,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609684},{"start":140609686,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140609686,"strand":1,"feature_type":"variation","id":"rs1054331390","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1331677740","clinical_significance":[],"alleles":["C","T"],"end":140609688,"strand":1,"feature_type":"variation","start":140609688,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140609693,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140609693,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1202535452"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799823746","alleles":["T","A","C"],"end":140609694,"feature_type":"variation","strand":1,"source":"dbSNP","start":140609694,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140609696,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140609696,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799823862","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609698,"feature_type":"variation","strand":1,"end":140609698,"alleles":["T","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1563176561"},{"clinical_significance":[],"seq_region_name":"7","id":"rs892955614","source":"dbSNP","start":140609701,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140609701,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1799824175","clinical_significance":[],"alleles":["T","C"],"end":140609704,"strand":1,"feature_type":"variation","start":140609704,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609705,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140609705,"clinical_significance":[],"seq_region_name":"7","id":"rs1563176570"},{"alleles":["T","C"],"end":140609708,"strand":1,"feature_type":"variation","start":140609708,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799824629","clinical_significance":[]},{"source":"dbSNP","start":140609716,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140609716,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1253035837"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609720,"feature_type":"variation","strand":1,"end":140609720,"alleles":["C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1225061504"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140609722,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609722,"source":"dbSNP","seq_region_name":"7","id":"rs1799824901","clinical_significance":[]},{"clinical_significance":[],"id":"rs1014928452","seq_region_name":"7","source":"dbSNP","start":140609726,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140609726,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140609727,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609727,"clinical_significance":[],"seq_region_name":"7","id":"rs1010507583"},{"source":"dbSNP","start":140609734,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TGTTGTT","TGTT"],"end":140609740,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799825209"},{"seq_region_name":"7","id":"rs1020343299","clinical_significance":[],"start":140609739,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140609746,"alleles":["TTCTTCTT","TTCTT"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140609741,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140609741,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799825434"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799825517","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609747,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140609747},{"end":140609754,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140609754,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs185534612","clinical_significance":[]},{"seq_region_name":"7","id":"rs907293204","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609756,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140609756},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140609757,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609757,"clinical_significance":[],"id":"rs998155979","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140609758,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609758,"clinical_significance":[],"seq_region_name":"7","id":"rs1466230124"},{"seq_region_name":"7","id":"rs1029264320","clinical_significance":[],"start":140609759,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140609759,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs189212290","clinical_significance":[],"strand":1,"feature_type":"variation","end":140609762,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609762,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799826141","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609766,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140609766},{"end":140609769,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140609769,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1343812517","clinical_significance":[]},{"id":"rs1208920543","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140609771,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609771,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1002840355","end":140609772,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140609772,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140609776,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140609776,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1034352933"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609778,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140609778,"id":"rs763957238","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140609783,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140609783,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1443140514","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799826845","clinical_significance":[],"alleles":["G","T"],"end":140609784,"strand":1,"feature_type":"variation","start":140609784,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs757726303","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609791,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140609791},{"end":140609793,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140609793,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1182552529","clinical_significance":[]},{"alleles":["G","T"],"end":140609797,"feature_type":"variation","strand":1,"source":"dbSNP","start":140609797,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799827140"},{"id":"rs1437905348","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","CC"],"end":140609798,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609798,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799827308","clinical_significance":[],"alleles":["A","G"],"end":140609799,"strand":1,"feature_type":"variation","start":140609799,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609800,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140609800,"clinical_significance":[],"id":"rs985034237","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1187067727","source":"dbSNP","start":140609801,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140609801,"alleles":["T","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1261629922","clinical_significance":[],"start":140609802,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140609802,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs756962820","clinical_significance":[],"strand":1,"feature_type":"variation","end":140609804,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609804,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140609805,"alleles":["A","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609805,"clinical_significance":[],"seq_region_name":"7","id":"rs1201055939"},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140609813,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609813,"clinical_significance":[],"seq_region_name":"7","id":"rs2130701344"},{"seq_region_name":"7","id":"rs1356946406","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609817,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140609817},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609820,"feature_type":"variation","strand":1,"end":140609820,"alleles":["G","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1314671288"},{"id":"rs778392944","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609822,"source":"dbSNP","strand":1,"feature_type":"variation","end":140609822,"alleles":["G","A"]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140609825,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609825,"clinical_significance":[],"id":"rs1799828548","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1469377273","alleles":["A","C"],"end":140609826,"feature_type":"variation","strand":1,"source":"dbSNP","start":140609826,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140609828,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140609828,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799828811","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609840,"feature_type":"variation","strand":1,"end":140609840,"alleles":["T","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1337628120"},{"start":140609841,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140609841,"alleles":["G","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799829069","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130701376","clinical_significance":[],"start":140609842,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140609842,"strand":1,"feature_type":"variation"},{"end":140609843,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140609843,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1327007810"},{"seq_region_name":"7","id":"rs1799829311","clinical_significance":[],"end":140609845,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140609845,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1390860294","feature_type":"variation","strand":1,"end":140609848,"alleles":["A","T"],"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609848},{"start":140609850,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","end":140609850,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799829581","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130701398","consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609851,"feature_type":"variation","strand":1,"end":140609851,"alleles":["G","T"]},{"start":140609856,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","alleles":["G","T"],"end":140609856,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs7810002","clinical_significance":[]},{"seq_region_name":"7","id":"rs918316108","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140609858,"source":"dbSNP","strand":1,"feature_type":"variation","end":140609858,"alleles":["A","G"]},{"feature_type":"variation","strand":1,"end":140609865,"alleles":["G","A"],"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609865,"clinical_significance":[],"seq_region_name":"7","id":"rs1799830059"},{"end":140609867,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140609867,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","seq_region_name":"7","id":"rs749975519","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140609871,"source":"dbSNP","strand":1,"feature_type":"variation","end":140609871,"alleles":["A","G"],"seq_region_name":"7","id":"rs1384925723","clinical_significance":[]},{"seq_region_name":"7","id":"rs1288129853","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140609876,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140609876},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140609877,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609877,"clinical_significance":[],"id":"rs1162549670","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799830753","source":"dbSNP","start":140609884,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","end":140609884,"alleles":["T","C","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs986392473","consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609886,"feature_type":"variation","strand":1,"end":140609889,"alleles":["CACA","CA"]},{"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140609888,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140609888,"seq_region_name":"7","id":"rs546272174","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140609894,"source":"dbSNP","strand":1,"feature_type":"variation","end":140609894,"alleles":["G","T"],"seq_region_name":"7","id":"rs1799831060","clinical_significance":[]},{"source":"dbSNP","start":140609898,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","end":140609898,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs138479282","seq_region_name":"7"},{"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609899,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140609899,"clinical_significance":[],"seq_region_name":"7","id":"rs192250658"},{"id":"rs1436705912","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140609900,"source":"dbSNP","strand":1,"feature_type":"variation","end":140609900,"alleles":["C","T"]},{"end":140609903,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140609903,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","seq_region_name":"7","id":"rs1799831449","clinical_significance":[]},{"end":140609907,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140609907,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs938378738"},{"strand":1,"feature_type":"variation","end":140609918,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140609918,"source":"dbSNP","seq_region_name":"7","id":"rs1056089866","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799831788","consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609919,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140609919},{"clinical_significance":[],"seq_region_name":"7","id":"rs1224580038","alleles":["C","G","T"],"end":140609921,"feature_type":"variation","strand":1,"source":"dbSNP","start":140609921,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1054280471","consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609924,"feature_type":"variation","strand":1,"alleles":["CCCCCC","CCCCC","CCCCCCC"],"end":140609929},{"seq_region_name":"7","id":"rs1799832209","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140609926,"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140609926,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799832396","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140609928,"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140609928,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs893071291","alleles":["C","T"],"end":140609929,"feature_type":"variation","strand":1,"source":"dbSNP","start":140609929,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38"},{"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609933,"feature_type":"variation","strand":1,"alleles":["-","A"],"end":140609932,"clinical_significance":[],"id":"rs2130701524","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130701528","consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609935,"feature_type":"variation","strand":1,"end":140609935,"alleles":["A","-"]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140609939,"assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","start":140609939,"source":"dbSNP","id":"rs915839298","seq_region_name":"7","clinical_significance":[]},{"start":140609942,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","end":140609942,"alleles":["C","CCTC"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130701533","clinical_significance":[]},{"start":140609943,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","end":140609943,"alleles":["A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1353157258","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130701546","clinical_significance":[],"start":140609944,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant","end":140609945,"alleles":["TT","TTCTT"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140609947,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609947,"clinical_significance":[],"id":"rs2130701553","seq_region_name":"7"},{"clinical_significance":[],"id":"rs2130701563","seq_region_name":"7","source":"dbSNP","start":140609951,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","end":140609951,"alleles":["C","-"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1277981038","clinical_significance":[],"end":140609952,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140609952,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140609953,"consequence_type":"non_coding_transcript_exon_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609953,"clinical_significance":[],"seq_region_name":"7","id":"rs1799832911"},{"seq_region_name":"7","id":"rs2130701575","clinical_significance":[],"end":140609953,"alleles":["-","CAGCTGGTAGCCA"],"strand":1,"feature_type":"variation","start":140609954,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"non_coding_transcript_exon_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609957,"feature_type":"variation","strand":1,"end":140609957,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799833006"},{"seq_region_name":"7","id":"rs2130701582","clinical_significance":[],"alleles":["-","ACAA"],"end":140609957,"strand":1,"feature_type":"variation","start":140609958,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["G","T"],"end":140609958,"feature_type":"variation","strand":1,"source":"dbSNP","start":140609958,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs945870669"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609959,"feature_type":"variation","strand":1,"end":140609959,"alleles":["T","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130701592"},{"seq_region_name":"7","id":"rs1799833193","clinical_significance":[],"strand":1,"feature_type":"variation","end":140609960,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609960,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140609961,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609961,"source":"dbSNP","seq_region_name":"7","id":"rs2130701599","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799833304","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609964,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140609964},{"start":140609965,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140609965,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs1041949040","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["CAATTACTC","-"],"end":140609974,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609966,"clinical_significance":[],"seq_region_name":"7","id":"rs2130701614"},{"end":140609968,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140609968,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs372515476","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1388486277","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609971,"feature_type":"variation","strand":1,"end":140609971,"alleles":["A","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1048257113","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609972,"feature_type":"variation","strand":1,"end":140609972,"alleles":["C","A"]},{"strand":1,"feature_type":"variation","end":140609975,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609975,"source":"dbSNP","seq_region_name":"7","id":"rs1799834106","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140609982,"alleles":["TTTTTTTT","TTTTTTTTT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609975,"source":"dbSNP","seq_region_name":"7","id":"rs1344267566","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140609978,"source":"dbSNP","strand":1,"feature_type":"variation","end":140609978,"alleles":["T","C"],"seq_region_name":"7","id":"rs2130701640","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609981,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140609981,"clinical_significance":[],"seq_region_name":"7","id":"rs1799834459"},{"feature_type":"variation","strand":1,"end":140609982,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609982,"clinical_significance":[],"seq_region_name":"7","id":"rs76432575"},{"start":140609983,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140609983,"alleles":["G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799834764","clinical_significance":[]},{"end":140609984,"alleles":["GG","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140609983,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130701653"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1228482239","source":"dbSNP","start":140609991,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140609991,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs149284658","clinical_significance":[],"alleles":["C","T"],"end":140609996,"strand":1,"feature_type":"variation","start":140609996,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs564722985","source":"dbSNP","start":140609997,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140609997,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140609999,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140609999,"clinical_significance":[],"seq_region_name":"7","id":"rs1799835464"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610001,"feature_type":"variation","strand":1,"end":140610001,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130701671"},{"id":"rs1799835616","seq_region_name":"7","clinical_significance":[],"alleles":["C","G","T"],"end":140610006,"strand":1,"feature_type":"variation","start":140610006,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140610010,"alleles":["G","C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610010,"clinical_significance":[],"seq_region_name":"7","id":"rs780375716"},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140610011,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610011,"source":"dbSNP","seq_region_name":"7","id":"rs1799835942","clinical_significance":[]},{"seq_region_name":"7","id":"rs1386750552","clinical_significance":[],"start":140610014,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140610014,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"start":140610019,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140610019,"alleles":["A","G"],"strand":1,"feature_type":"variation","id":"rs2130701697","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140610020,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610020,"source":"dbSNP","seq_region_name":"7","id":"rs2130701705","clinical_significance":[]},{"source":"dbSNP","start":140610023,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140610023,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1003366928"},{"seq_region_name":"7","id":"rs375582256","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","C","T"],"end":140610025,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610025,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610029,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140610029,"clinical_significance":[],"seq_region_name":"7","id":"rs745374712"},{"source":"dbSNP","start":140610031,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140610031,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1268055878"},{"seq_region_name":"7","id":"rs894467151","clinical_significance":[],"end":140610039,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140610039,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1212105964","source":"dbSNP","start":140610043,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140610043,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1265900922","alleles":["C","T"],"end":140610044,"feature_type":"variation","strand":1,"source":"dbSNP","start":140610044,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs997538696","clinical_significance":[],"end":140610045,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140610045,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140610050,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610050,"clinical_significance":[],"seq_region_name":"7","id":"rs1480113437"},{"alleles":["C","G","T"],"end":140610053,"strand":1,"feature_type":"variation","start":140610053,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs115047234","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610059,"feature_type":"variation","strand":1,"end":140610059,"alleles":["G","C"],"clinical_significance":[],"id":"rs889376807","seq_region_name":"7"},{"start":140610060,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140610060,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs1011822249","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610068,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140610068,"clinical_significance":[],"seq_region_name":"7","id":"rs747583157"},{"strand":1,"feature_type":"variation","end":140610069,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610069,"source":"dbSNP","seq_region_name":"7","id":"rs967547377","clinical_significance":[]},{"source":"dbSNP","start":140610070,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140610070,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799837683"},{"end":140610071,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140610071,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1585750522","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1345483394","source":"dbSNP","start":140610073,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140610073,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1585750531","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610074,"source":"dbSNP","strand":1,"feature_type":"variation","end":140610074,"alleles":["T","C"]},{"strand":1,"feature_type":"variation","end":140610076,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610076,"source":"dbSNP","seq_region_name":"7","id":"rs1799838071","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610077,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140610077,"seq_region_name":"7","id":"rs977118472","clinical_significance":[]},{"alleles":["G","A"],"end":140610078,"feature_type":"variation","strand":1,"source":"dbSNP","start":140610078,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1158063887"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610079,"source":"dbSNP","strand":1,"feature_type":"variation","end":140610079,"alleles":["C","T"],"seq_region_name":"7","id":"rs972226430","clinical_significance":[]},{"end":140610085,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140610085,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799838484","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610088,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140610088,"seq_region_name":"7","id":"rs1799838586","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140610091,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610091,"source":"dbSNP","id":"rs1315791501","seq_region_name":"7","clinical_significance":[]},{"end":140610096,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140610096,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130701821"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1350210823","end":140610097,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140610097,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140610100,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140610100,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1399699799","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1030920656","source":"dbSNP","start":140610102,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140610102,"alleles":["A","G"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140610105,"alleles":["A","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610105,"source":"dbSNP","seq_region_name":"7","id":"rs1035458745","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140610106,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610106,"clinical_significance":[],"seq_region_name":"7","id":"rs1799839216"},{"strand":1,"feature_type":"variation","end":140610107,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610107,"source":"dbSNP","id":"rs1799839329","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1459268303","end":140610109,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140610109,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140610112,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140610112,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799839531"},{"start":140610117,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140610117,"alleles":["C","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799839624","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799839709","source":"dbSNP","start":140610119,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140610119,"alleles":["C","T"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610120,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140610120,"seq_region_name":"7","id":"rs755228640","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799840009","feature_type":"variation","strand":1,"end":140610122,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610122},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140610123,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610123,"source":"dbSNP","seq_region_name":"7","id":"rs2130701882","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799840100","feature_type":"variation","strand":1,"end":140610124,"alleles":["AT","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610123},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140610124,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610124,"clinical_significance":[],"id":"rs1428543225","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140610125,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610125,"clinical_significance":[],"seq_region_name":"7","id":"rs1799840282"},{"seq_region_name":"7","id":"rs1364888874","clinical_significance":[],"strand":1,"feature_type":"variation","end":140610126,"alleles":["T","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610126,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610127,"source":"dbSNP","strand":1,"feature_type":"variation","end":140610127,"alleles":["G","A"],"seq_region_name":"7","id":"rs1799840505","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799840620","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140610128,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610128},{"source":"dbSNP","start":140610129,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140610129,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1186994437"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610130,"feature_type":"variation","strand":1,"end":140610130,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799840805"},{"start":140610133,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140610133,"alleles":["T","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799840894","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1240081452","alleles":["A","T"],"end":140610135,"feature_type":"variation","strand":1,"source":"dbSNP","start":140610135,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs10709637","feature_type":"variation","strand":1,"end":140610142,"alleles":["AAAAAAAA","AAAAAAA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610135},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610141,"feature_type":"variation","strand":1,"end":140610143,"alleles":["AAT","-"],"clinical_significance":[],"id":"rs80355631","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs55633923","alleles":["A","T"],"end":140610142,"feature_type":"variation","strand":1,"source":"dbSNP","start":140610142,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140610142,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140610143,"alleles":["AT","-"],"strand":1,"feature_type":"variation","id":"rs1309375447","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140610143,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610143,"clinical_significance":[],"seq_region_name":"7","id":"rs991175448"},{"strand":1,"feature_type":"variation","alleles":["TTTTTTTT","TTTT","TTTTTTT","TTTTTTTTT"],"end":140610150,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610143,"source":"dbSNP","seq_region_name":"7","id":"rs537471796","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140610144,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610144,"clinical_significance":[],"seq_region_name":"7","id":"rs1201906080"},{"seq_region_name":"7","id":"rs1639967","clinical_significance":[],"strand":1,"feature_type":"variation","end":140610155,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610155,"source":"dbSNP"},{"alleles":["GGGG","GGG"],"end":140610163,"strand":1,"feature_type":"variation","start":140610160,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799842050","clinical_significance":[]},{"end":140610161,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140610161,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs911001834","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1274361419","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140610166,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610166},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799842339","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610168,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140610168},{"clinical_significance":[],"seq_region_name":"7","id":"rs1348210012","source":"dbSNP","start":140610169,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140610169,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1222814971","seq_region_name":"7","end":140610171,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140610171,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140610174,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140610174,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799842705","clinical_significance":[]},{"source":"dbSNP","start":140610176,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140610176,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799842803"},{"seq_region_name":"7","id":"rs915602564","clinical_significance":[],"strand":1,"feature_type":"variation","end":140610179,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610179,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140610181,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610181,"clinical_significance":[],"seq_region_name":"7","id":"rs1453835607"},{"alleles":["G","A","C"],"end":140610185,"feature_type":"variation","strand":1,"source":"dbSNP","start":140610185,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1383131576","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs931212261","source":"dbSNP","start":140610186,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140610186,"alleles":["G","A","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1338236792","clinical_significance":[],"alleles":["C","G"],"end":140610188,"strand":1,"feature_type":"variation","start":140610188,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610191,"source":"dbSNP","strand":1,"feature_type":"variation","end":140610191,"alleles":["G","A"],"seq_region_name":"7","id":"rs575277143","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799843618","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610197,"feature_type":"variation","strand":1,"end":140610197,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs536203841","source":"dbSNP","start":140610198,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140610198,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799843800","source":"dbSNP","start":140610199,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140610199,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1799843897","clinical_significance":[],"alleles":["GCTCAAGCAATCCTC","-"],"end":140610215,"strand":1,"feature_type":"variation","start":140610201,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1799843989","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140610206,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610206,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140610218,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610218,"source":"dbSNP","seq_region_name":"7","id":"rs1585750806","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799844189","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140610219,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610219,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610220,"feature_type":"variation","strand":1,"end":140610220,"alleles":["C","T"],"clinical_significance":[],"id":"rs1264200427","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799844411","end":140610221,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140610221,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799844513","source":"dbSNP","start":140610230,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140610230,"alleles":["C","T"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610232,"feature_type":"variation","strand":1,"end":140610232,"alleles":["A","G"],"clinical_significance":[],"id":"rs184588480","seq_region_name":"7"},{"end":140610233,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140610233,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1799844734","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","G"],"end":140610239,"feature_type":"variation","strand":1,"source":"dbSNP","start":140610239,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799844844"},{"start":140610241,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140610241,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799844945","clinical_significance":[]},{"start":140610242,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140610242,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799845063","clinical_significance":[]},{"seq_region_name":"7","id":"rs1417289193","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610247,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140610247},{"alleles":["A","G","T"],"end":140610249,"feature_type":"variation","strand":1,"source":"dbSNP","start":140610249,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1036824883"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140610250,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610250,"source":"dbSNP","seq_region_name":"7","id":"rs1444998025","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799845463","source":"dbSNP","start":140610256,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140610256,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs901932547","seq_region_name":"7","alleles":["T","C"],"end":140610260,"feature_type":"variation","strand":1,"source":"dbSNP","start":140610260,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs547156099","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610265,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140610265},{"seq_region_name":"7","id":"rs71522105","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610272,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","CC"],"end":140610272},{"start":140610274,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140610274,"alleles":["C","CC"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs71522106","clinical_significance":[]},{"alleles":["C","T"],"end":140610274,"strand":1,"feature_type":"variation","start":140610274,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799845894","clinical_significance":[]},{"id":"rs1799846107","seq_region_name":"7","clinical_significance":[],"start":140610280,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140610280,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140610287,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610287,"source":"dbSNP","id":"rs1050445671","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799846298","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610287,"feature_type":"variation","strand":1,"end":140610288,"alleles":["AA","AAA"]},{"end":140610289,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140610289,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585750891"},{"seq_region_name":"7","id":"rs1799846528","clinical_significance":[],"start":140610289,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["GG","G"],"end":140610290,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799846711","source":"dbSNP","start":140610290,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140610289,"alleles":["-","A"],"feature_type":"variation","strand":1},{"start":140610290,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140610290,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1233475018","clinical_significance":[]},{"start":140610291,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C","G"],"end":140610291,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799847028","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs576801972","source":"dbSNP","start":140610291,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AAAAAAAAAAAAAAAAAA","AAAAAAAAA","AAAAAAAAAAAAAA","AAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAAAA"],"end":140610308,"feature_type":"variation","strand":1},{"alleles":["A","G"],"end":140610292,"strand":1,"feature_type":"variation","start":140610292,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1799847576","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1491175351","alleles":["AAA","AAAGAAA"],"end":140610294,"feature_type":"variation","strand":1,"source":"dbSNP","start":140610292,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1799847811","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610294,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140610294},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610295,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140610295,"clinical_significance":[],"seq_region_name":"7","id":"rs889148611"},{"source":"dbSNP","start":140610300,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140610300,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130702202"},{"seq_region_name":"7","id":"rs80276942","clinical_significance":[],"end":140610307,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140610307,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799848127","alleles":["A","C","G"],"end":140610308,"feature_type":"variation","strand":1,"source":"dbSNP","start":140610308,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs79825488","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610309,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140610309},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140610310,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610310,"source":"dbSNP","seq_region_name":"7","id":"rs75206994","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130702219","clinical_significance":[],"alleles":["C","A"],"end":140610311,"strand":1,"feature_type":"variation","start":140610311,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1430381505","alleles":["G","T"],"end":140610313,"feature_type":"variation","strand":1,"source":"dbSNP","start":140610313,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140610317,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610317,"clinical_significance":[],"seq_region_name":"7","id":"rs928455472"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610319,"source":"dbSNP","strand":1,"feature_type":"variation","end":140610319,"alleles":["A","G"],"seq_region_name":"7","id":"rs912566730","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610325,"source":"dbSNP","strand":1,"feature_type":"variation","end":140610325,"alleles":["T","C"],"id":"rs965487857","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585751033","source":"dbSNP","start":140610326,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140610326,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130702239","alleles":["A","C"],"end":140610331,"feature_type":"variation","strand":1,"source":"dbSNP","start":140610331,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1799849025","clinical_significance":[],"alleles":["T","C"],"end":140610333,"strand":1,"feature_type":"variation","start":140610333,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799849117","source":"dbSNP","start":140610338,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140610338,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610339,"feature_type":"variation","strand":1,"end":140610339,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1443699624"},{"alleles":["T","A"],"end":140610340,"strand":1,"feature_type":"variation","start":140610340,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1170451272","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140610341,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610341,"clinical_significance":[],"seq_region_name":"7","id":"rs1799849416"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799849511","source":"dbSNP","start":140610342,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140610342,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585751053","source":"dbSNP","start":140610344,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140610344,"alleles":["G","C","T"],"feature_type":"variation","strand":1},{"id":"rs1799849737","seq_region_name":"7","clinical_significance":[],"start":140610345,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140610345,"strand":1,"feature_type":"variation"},{"id":"rs1352743151","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610346,"source":"dbSNP","strand":1,"feature_type":"variation","end":140610346,"alleles":["T","A"]},{"seq_region_name":"7","id":"rs1011771381","clinical_significance":[],"strand":1,"feature_type":"variation","end":140610349,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610349,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799850030","source":"dbSNP","start":140610353,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140610353,"feature_type":"variation","strand":1},{"alleles":["G","A"],"end":140610354,"feature_type":"variation","strand":1,"source":"dbSNP","start":140610354,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799850178"},{"start":140610355,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","T"],"end":140610355,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1021851216","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1386790002","source":"dbSNP","start":140610356,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140610356,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1161923189","feature_type":"variation","strand":1,"end":140610357,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610357},{"start":140610361,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140610361,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585751109","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs903333231","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610364,"feature_type":"variation","strand":1,"end":140610364,"alleles":["C","G","T"]},{"source":"dbSNP","start":140610365,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140610365,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs144551578"},{"seq_region_name":"7","id":"rs1799850771","clinical_significance":[],"start":140610368,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140610368,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"id":"rs1799850862","seq_region_name":"7","clinical_significance":[],"end":140610369,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140610369,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140610370,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140610370,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1440860826"},{"start":140610382,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140610382,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs1799851071","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610385,"feature_type":"variation","strand":1,"end":140610385,"alleles":["G","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1179069030"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140610386,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610386,"clinical_significance":[],"id":"rs1035810073","seq_region_name":"7"},{"alleles":["C","A"],"end":140610399,"strand":1,"feature_type":"variation","start":140610399,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1303000397","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610400,"feature_type":"variation","strand":1,"end":140610400,"alleles":["C","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799851456"},{"seq_region_name":"7","id":"rs1585751177","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140610403,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610403,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799851648","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610404,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140610404},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140610407,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610407,"source":"dbSNP","id":"rs959816153","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs540483919","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610408,"feature_type":"variation","strand":1,"end":140610408,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1313438384","clinical_significance":[],"start":140610411,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140610411,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610418,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140610418,"clinical_significance":[],"seq_region_name":"7","id":"rs2130702399"},{"end":140610425,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140610425,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1359309343","clinical_significance":[]},{"start":140610431,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140610444,"alleles":["GAGAGAGAGAGAGA","GAGAGAGAGA","GAGAGAGAGAGA","GAGAGAGAGAGAGAGA"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1006201413","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1320785269","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610433,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140610433},{"strand":1,"feature_type":"variation","end":140610435,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610435,"source":"dbSNP","seq_region_name":"7","id":"rs148057821","clinical_significance":[]},{"alleles":["G","C"],"end":140610437,"strand":1,"feature_type":"variation","start":140610437,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1022618932","clinical_significance":[]},{"id":"rs577344876","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610439,"source":"dbSNP","strand":1,"feature_type":"variation","end":140610439,"alleles":["G","C"]},{"start":140610443,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C"],"end":140610443,"strand":1,"feature_type":"variation","id":"rs1277421679","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799853131","source":"dbSNP","start":140610446,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140610446,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1799853212","seq_region_name":"7","source":"dbSNP","start":140610449,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140610449,"alleles":["G","C"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610451,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140610451,"clinical_significance":[],"seq_region_name":"7","id":"rs1305779817"},{"end":140610454,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140610454,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1367358489"},{"alleles":["A","G"],"end":140610457,"feature_type":"variation","strand":1,"source":"dbSNP","start":140610457,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs955034271","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs143779213","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610458,"feature_type":"variation","strand":1,"end":140610458,"alleles":["T","C","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799853690","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610459,"feature_type":"variation","strand":1,"end":140610459,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799853786","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610460,"feature_type":"variation","strand":1,"end":140610460,"alleles":["G","A"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610461,"source":"dbSNP","strand":1,"feature_type":"variation","end":140610461,"alleles":["T","C"],"seq_region_name":"7","id":"rs1238262281","clinical_significance":[]},{"seq_region_name":"7","id":"rs1007697472","clinical_significance":[],"start":140610465,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140610465,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799854287","end":140610468,"alleles":["C","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140610468,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140610471,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140610471,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1017957008","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799854441","source":"dbSNP","start":140610473,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140610473,"feature_type":"variation","strand":1},{"end":140610477,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140610477,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799854540","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799854707","feature_type":"variation","strand":1,"end":140610479,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610479},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799854832","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140610492,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610492},{"clinical_significance":[],"seq_region_name":"7","id":"rs963769185","feature_type":"variation","strand":1,"end":140610498,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610498},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140610505,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610505,"source":"dbSNP","seq_region_name":"7","id":"rs1799855159","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799855319","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610508,"feature_type":"variation","strand":1,"end":140610508,"alleles":["C","G"]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140610510,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610510,"clinical_significance":[],"id":"rs984012599","seq_region_name":"7"},{"alleles":["C","G","T"],"end":140610512,"strand":1,"feature_type":"variation","start":140610512,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs188238538","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs781629295","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610517,"feature_type":"variation","strand":1,"end":140610517,"alleles":["A","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610518,"feature_type":"variation","strand":1,"end":140610518,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1483198980"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1267341663","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140610524,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610524},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610528,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140610528,"seq_region_name":"7","id":"rs562273973","clinical_significance":[]},{"seq_region_name":"7","id":"rs914215614","clinical_significance":[],"alleles":["TATATATATATAT","TATATATAT","TATATATATAT","TATATATATATATAT"],"end":140610541,"strand":1,"feature_type":"variation","start":140610529,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1260978893","clinical_significance":[],"alleles":["T","G"],"end":140610531,"strand":1,"feature_type":"variation","start":140610531,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1799856867","clinical_significance":[],"start":140610533,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140610533,"strand":1,"feature_type":"variation"},{"alleles":["TATATGTATAT","TATATGTATATGTATAT"],"end":140610547,"strand":1,"feature_type":"variation","start":140610537,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799857001","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799857153","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140610538,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610538},{"clinical_significance":[],"seq_region_name":"7","id":"rs775350436","source":"dbSNP","start":140610541,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A","C"],"end":140610541,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140610542,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610542,"source":"dbSNP","seq_region_name":"7","id":"rs933411933","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799857691","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610546,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140610546},{"source":"dbSNP","start":140610547,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140610547,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585751448"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610549,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140610549,"clinical_significance":[],"seq_region_name":"7","id":"rs928598460"},{"seq_region_name":"7","id":"rs938466716","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610555,"source":"dbSNP","strand":1,"feature_type":"variation","end":140610555,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1799858324","clinical_significance":[],"strand":1,"feature_type":"variation","end":140610556,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610556,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610558,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140610558,"clinical_significance":[],"seq_region_name":"7","id":"rs1799858482"},{"seq_region_name":"7","id":"rs1050971105","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610560,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140610560},{"start":140610564,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140610565,"alleles":["CC","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1055654320","clinical_significance":[]},{"alleles":["A","T"],"end":140610566,"strand":1,"feature_type":"variation","start":140610566,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs889096674","clinical_significance":[]},{"source":"dbSNP","start":140610571,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140610571,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799859084"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799859240","source":"dbSNP","start":140610572,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140610572,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140610573,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610573,"source":"dbSNP","seq_region_name":"7","id":"rs915957813","clinical_significance":[]},{"end":140610575,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140610575,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585751513","clinical_significance":[]},{"alleles":["T","C"],"end":140610577,"feature_type":"variation","strand":1,"source":"dbSNP","start":140610577,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799859535"},{"seq_region_name":"7","id":"rs942100258","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["ACACAC","ACACACAC"],"end":140610585,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610580,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1388258397","feature_type":"variation","strand":1,"end":140610581,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610581},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140610584,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610584,"clinical_significance":[],"id":"rs1451966478","seq_region_name":"7"},{"source":"dbSNP","start":140610585,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140610585,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs548972373","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140610587,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610587,"clinical_significance":[],"seq_region_name":"7","id":"rs2130702681"},{"seq_region_name":"7","id":"rs1043255252","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610588,"source":"dbSNP","strand":1,"feature_type":"variation","end":140610588,"alleles":["T","C","G"]},{"start":140610588,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140610593,"alleles":["TTTTTT","TTTTT","TTTTTTT"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs897815595","clinical_significance":[]},{"start":140610590,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140610590,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs1799860406","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","T"],"end":140610601,"feature_type":"variation","strand":1,"source":"dbSNP","start":140610601,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799860508"},{"strand":1,"feature_type":"variation","alleles":["GGGG","GGG"],"end":140610607,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610604,"source":"dbSNP","id":"rs1198729590","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799860783","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140610606,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610606},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610607,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140610607,"seq_region_name":"7","id":"rs59500330","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs999553265","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610610,"feature_type":"variation","strand":1,"end":140610610,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs528421400","source":"dbSNP","start":140610614,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140610614,"alleles":["A","G"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610615,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140610615,"clinical_significance":[],"seq_region_name":"7","id":"rs546559102"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799861281","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140610619,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610619},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610623,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140610623,"seq_region_name":"7","id":"rs1799861382","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799861479","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140610624,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610624,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610624,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GTCAAGTCA","GTCA"],"end":140610632,"seq_region_name":"7","id":"rs890733782","clinical_significance":[]},{"alleles":["A","G"],"end":140610641,"feature_type":"variation","strand":1,"source":"dbSNP","start":140610641,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799861715"},{"feature_type":"variation","strand":1,"end":140610644,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610644,"clinical_significance":[],"id":"rs896003375","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1267068145","source":"dbSNP","start":140610647,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140610647,"alleles":["A","G"],"feature_type":"variation","strand":1},{"start":140610650,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140610650,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799862009","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585751647","clinical_significance":[],"start":140610654,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140610654,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1799862207","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610655,"source":"dbSNP","strand":1,"feature_type":"variation","end":140610655,"alleles":["T","C"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610659,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140610659,"seq_region_name":"7","id":"rs1382430746","clinical_significance":[]},{"id":"rs1563177200","seq_region_name":"7","clinical_significance":[],"start":140610671,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140610671,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1017736956","clinical_significance":[],"strand":1,"feature_type":"variation","end":140610672,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610672,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610681,"source":"dbSNP","strand":1,"feature_type":"variation","end":140610681,"alleles":["C","G"],"seq_region_name":"7","id":"rs1012653291","clinical_significance":[]},{"seq_region_name":"7","id":"rs958235114","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610682,"source":"dbSNP","strand":1,"feature_type":"variation","end":140610682,"alleles":["A","G"]},{"start":140610682,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","-"],"end":140610682,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799862769","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799862858","source":"dbSNP","start":140610683,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140610683,"feature_type":"variation","strand":1},{"id":"rs1799863008","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140610687,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610687,"source":"dbSNP"},{"source":"dbSNP","start":140610691,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140610691,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1300356149"},{"seq_region_name":"7","id":"rs1261179678","clinical_significance":[],"start":140610695,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140610695,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"start":140610698,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140610698,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799863316","clinical_significance":[]},{"start":140610699,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140610699,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs773391659","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799863640","clinical_significance":[],"start":140610700,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140610700,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"id":"rs1585751716","seq_region_name":"7","clinical_significance":[],"start":140610701,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140610701,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799863971","source":"dbSNP","start":140610702,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140610702,"feature_type":"variation","strand":1},{"id":"rs1799864119","seq_region_name":"7","clinical_significance":[],"start":140610705,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140610705,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"start":140610706,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140610706,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799864261","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140610709,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610709,"source":"dbSNP","seq_region_name":"7","id":"rs952326353","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799864541","alleles":["G","C"],"end":140610714,"feature_type":"variation","strand":1,"source":"dbSNP","start":140610714,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1279478982","source":"dbSNP","start":140610723,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140610723,"alleles":["C","A","T"],"feature_type":"variation","strand":1},{"id":"rs1799864754","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610728,"source":"dbSNP","strand":1,"feature_type":"variation","end":140610728,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1380281440","clinical_significance":[],"start":140610734,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140610734,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs2130702874","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610735,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140610735},{"clinical_significance":[],"seq_region_name":"7","id":"rs1314056668","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610736,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140610736},{"clinical_significance":[],"id":"rs1201958502","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610742,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140610742},{"end":140610745,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140610745,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799865171","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140610750,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610750,"clinical_significance":[],"seq_region_name":"7","id":"rs1799865261"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1262770611","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610757,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140610757},{"source":"dbSNP","start":140610758,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140610758,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs181075365"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1015479783","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140610762,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610762},{"clinical_significance":[],"seq_region_name":"7","id":"rs201243655","source":"dbSNP","start":140610763,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C","G"],"end":140610763,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140610771,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610771,"source":"dbSNP","id":"rs1799865780","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140610787,"alleles":["GGAGGAGGA","GGAGGA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610779,"source":"dbSNP","seq_region_name":"7","id":"rs1462997850","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140610782,"alleles":["G","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610782,"clinical_significance":[],"seq_region_name":"7","id":"rs967435525"},{"source":"dbSNP","start":140610787,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["ACCAAGAGAA","A"],"end":140610796,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1449221441","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["C","A","G"],"end":140610789,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610789,"source":"dbSNP","id":"rs1247058990","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799866312","source":"dbSNP","start":140610790,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140610790,"alleles":["A","C"],"feature_type":"variation","strand":1},{"id":"rs1799866391","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140610797,"strand":1,"feature_type":"variation","start":140610797,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs114578380","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610798,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140610798},{"clinical_significance":[],"id":"rs1475071541","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140610799,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610799},{"clinical_significance":[],"seq_region_name":"7","id":"rs1183746401","end":140610801,"alleles":["GGG","GGGG"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140610799,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610800,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140610800,"clinical_significance":[],"seq_region_name":"7","id":"rs1199379902"},{"id":"rs1799866954","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140610801,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610801,"source":"dbSNP"},{"end":140610802,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140610802,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1191238321","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799867158","clinical_significance":[],"end":140610806,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140610806,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140610812,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140610812,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799867256"},{"seq_region_name":"7","id":"rs1585751876","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610813,"source":"dbSNP","strand":1,"feature_type":"variation","end":140610813,"alleles":["G","A"]},{"source":"dbSNP","start":140610815,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140610815,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs749425399"},{"seq_region_name":"7","id":"rs959947528","clinical_significance":[],"alleles":["GGAGCGGAGC","GGAGC"],"end":140610828,"strand":1,"feature_type":"variation","start":140610819,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1799867700","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610820,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140610820},{"source":"dbSNP","start":140610822,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140610822,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1341148616"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610823,"feature_type":"variation","strand":1,"end":140610823,"alleles":["C","A","T"],"clinical_significance":[],"id":"rs550671562","seq_region_name":"7"},{"id":"rs568961750","seq_region_name":"7","clinical_significance":[],"start":140610824,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140610824,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140610829,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610829,"source":"dbSNP","seq_region_name":"7","id":"rs1799868146","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140610830,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610830,"clinical_significance":[],"seq_region_name":"7","id":"rs1333673479"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1175191838","feature_type":"variation","strand":1,"alleles":["GGACCCGG","GGACCCGGACCCGG"],"end":140610844,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610837},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799868450","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140610838,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610838},{"clinical_significance":[],"id":"rs973874557","seq_region_name":"7","feature_type":"variation","strand":1,"end":140610840,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610840},{"clinical_significance":[],"seq_region_name":"7","id":"rs922447574","end":140610842,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140610842,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["G","A","C"],"end":140610843,"feature_type":"variation","strand":1,"source":"dbSNP","start":140610843,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs553494429","seq_region_name":"7"},{"clinical_significance":[],"id":"rs529541035","seq_region_name":"7","end":140610845,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140610845,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1799869323","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610846,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140610846},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140610847,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610847,"clinical_significance":[],"seq_region_name":"7","id":"rs1165843111"},{"clinical_significance":[],"seq_region_name":"7","id":"rs890675945","source":"dbSNP","start":140610848,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140610848,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1366318266","seq_region_name":"7","source":"dbSNP","start":140610850,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140610850,"alleles":["C","G","T"],"feature_type":"variation","strand":1},{"end":140610851,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140610851,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1799870087","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1343921826","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610861,"feature_type":"variation","strand":1,"end":140610866,"alleles":["CTGCTG","CTG"]},{"source":"dbSNP","start":140610863,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140610863,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1437855101","seq_region_name":"7"},{"end":140610868,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140610868,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs2130703089","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140610869,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610869,"clinical_significance":[],"seq_region_name":"7","id":"rs1799870553"},{"alleles":["C","G"],"end":140610870,"strand":1,"feature_type":"variation","start":140610870,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs910645039","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799870778","source":"dbSNP","start":140610873,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["CCCC","CCC"],"end":140610876,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1799870873","clinical_significance":[],"start":140610874,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140610874,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140610877,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610877,"clinical_significance":[],"seq_region_name":"7","id":"rs1202855837"},{"id":"rs1799871078","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140610879,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610879,"source":"dbSNP"},{"start":140610884,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140610884,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1482614465","clinical_significance":[]},{"source":"dbSNP","start":140610884,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TCTTTCTT","TCTT"],"end":140610891,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799871275"},{"id":"rs184021629","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140610887,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610887,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1224438336","clinical_significance":[],"start":140610889,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140610889,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140610892,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140610892,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799871581"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610906,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140610906,"clinical_significance":[],"seq_region_name":"7","id":"rs1799871681"},{"alleles":["C","T"],"end":140610912,"feature_type":"variation","strand":1,"source":"dbSNP","start":140610912,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs2130703153","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799871788","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140610919,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610919,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1354563529","clinical_significance":[],"end":140610923,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140610923,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1799871986","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610925,"source":"dbSNP","strand":1,"feature_type":"variation","end":140610925,"alleles":["C","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1043037847","source":"dbSNP","start":140610926,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140610926,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799872205","end":140610929,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140610929,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1799872288","seq_region_name":"7","clinical_significance":[],"start":140610934,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140610934,"strand":1,"feature_type":"variation"},{"id":"rs1239891200","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140610935,"strand":1,"feature_type":"variation","start":140610935,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610937,"feature_type":"variation","strand":1,"end":140610937,"alleles":["G","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs554506861"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799872603","feature_type":"variation","strand":1,"end":140610942,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610942},{"alleles":["A","C"],"end":140610945,"strand":1,"feature_type":"variation","start":140610945,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799872690","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140610946,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610946,"source":"dbSNP","seq_region_name":"7","id":"rs1799872796","clinical_significance":[]},{"alleles":["C","G"],"end":140610948,"strand":1,"feature_type":"variation","start":140610948,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799872893","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs368838923","alleles":["C","T"],"end":140610952,"feature_type":"variation","strand":1,"source":"dbSNP","start":140610952,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140610954,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140610954,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs547824486"},{"feature_type":"variation","strand":1,"end":140610955,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610955,"clinical_significance":[],"seq_region_name":"7","id":"rs2130703220"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1330148583","alleles":["C","G","T"],"end":140610957,"feature_type":"variation","strand":1,"source":"dbSNP","start":140610957,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs36120875","feature_type":"variation","strand":1,"end":140610958,"alleles":["CC","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610957},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610958,"source":"dbSNP","strand":1,"feature_type":"variation","end":140610958,"alleles":["C","A"],"seq_region_name":"7","id":"rs1305377900","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799873933","source":"dbSNP","start":140610963,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140610963,"alleles":["G","T"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140610964,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140610964,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1057511013"},{"end":140610965,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140610965,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs902950983","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs895964338","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140610967,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610967},{"alleles":["C","A","T"],"end":140610973,"feature_type":"variation","strand":1,"source":"dbSNP","start":140610973,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1162236696"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140610975,"feature_type":"variation","strand":1,"end":140610975,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799874570"},{"seq_region_name":"7","id":"rs1799874741","clinical_significance":[],"start":140610979,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140610979,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"id":"rs1799874866","seq_region_name":"7","clinical_significance":[],"end":140610981,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140610981,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1364969077","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140610988,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610988,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1210338770","end":140610989,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140610989,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","T"],"end":140610996,"strand":1,"feature_type":"variation","start":140610996,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130703273","clinical_significance":[]},{"id":"rs1799875187","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["CTGA","-"],"end":140611000,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140610997,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799875302","clinical_significance":[],"alleles":["G","A"],"end":140610999,"strand":1,"feature_type":"variation","start":140610999,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611000,"source":"dbSNP","strand":1,"feature_type":"variation","end":140611000,"alleles":["A","G"],"id":"rs1799875410","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799875495","source":"dbSNP","start":140611004,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140611004,"alleles":["C","A"],"feature_type":"variation","strand":1},{"start":140611011,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G","T"],"end":140611011,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1179372916","clinical_significance":[]},{"clinical_significance":[],"id":"rs73736642","seq_region_name":"7","end":140611013,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140611013,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140611014,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C","T"],"end":140611014,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs763786191"},{"seq_region_name":"7","id":"rs1289473780","clinical_significance":[],"alleles":["ACC","-"],"end":140611018,"strand":1,"feature_type":"variation","start":140611016,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140611017,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140611017,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799876336"},{"feature_type":"variation","strand":1,"alleles":["C","A","G","T"],"end":140611018,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611018,"clinical_significance":[],"id":"rs73500495","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140611019,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611019,"source":"dbSNP","seq_region_name":"7","id":"rs1266383361","clinical_significance":[]},{"seq_region_name":"7","id":"rs557116204","clinical_significance":[],"start":140611030,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A","C"],"end":140611030,"strand":1,"feature_type":"variation"},{"id":"rs1015259191","seq_region_name":"7","clinical_significance":[],"alleles":["A","G"],"end":140611031,"strand":1,"feature_type":"variation","start":140611031,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611034,"source":"dbSNP","strand":1,"feature_type":"variation","end":140611034,"alleles":["A","G"],"seq_region_name":"7","id":"rs1285692974","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563177433","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140611038,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611038},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799877145","alleles":["A","G"],"end":140611039,"feature_type":"variation","strand":1,"source":"dbSNP","start":140611039,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1434798689","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140611040,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611040},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611043,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TTATTATTATTATTATT","TTATTATTATTATT","TTATTATTATTATTATTATT"],"end":140611059,"seq_region_name":"7","id":"rs963180883","clinical_significance":[]},{"end":140611045,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140611045,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799877449","clinical_significance":[]},{"source":"dbSNP","start":140611046,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A","C"],"end":140611046,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1400991001"},{"feature_type":"variation","strand":1,"end":140611050,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611050,"clinical_significance":[],"id":"rs1799877676","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799877771","feature_type":"variation","strand":1,"end":140611051,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611051},{"source":"dbSNP","start":140611053,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140611053,"alleles":["T","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799877861","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs973281331","end":140611054,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140611054,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["A","-"],"end":140611054,"strand":1,"feature_type":"variation","start":140611054,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799878054","clinical_significance":[]},{"seq_region_name":"7","id":"rs961363340","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611055,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140611055},{"feature_type":"variation","strand":1,"end":140611056,"alleles":["TT","TTT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611055,"clinical_significance":[],"seq_region_name":"7","id":"rs1386678969"},{"clinical_significance":[],"id":"rs1799878380","seq_region_name":"7","source":"dbSNP","start":140611056,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140611058,"alleles":["TAT","T"],"feature_type":"variation","strand":1},{"id":"rs9691566","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611057,"source":"dbSNP","strand":1,"feature_type":"variation","end":140611057,"alleles":["A","T"]},{"alleles":["A","-"],"end":140611057,"feature_type":"variation","strand":1,"source":"dbSNP","start":140611057,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799878624"},{"seq_region_name":"7","id":"rs1799878715","clinical_significance":[],"strand":1,"feature_type":"variation","end":140611059,"alleles":["TT","TTGTT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611058,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140611060,"alleles":["T","A","C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611060,"clinical_significance":[],"seq_region_name":"7","id":"rs1030012400"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799878968","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611061,"feature_type":"variation","strand":1,"end":140611061,"alleles":["T","G"]},{"feature_type":"variation","strand":1,"end":140611062,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611062,"clinical_significance":[],"seq_region_name":"7","id":"rs1245967107"},{"start":140611064,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140611064,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs953869820","clinical_significance":[]},{"source":"dbSNP","start":140611065,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140611065,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799879257"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140611068,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611068,"source":"dbSNP","seq_region_name":"7","id":"rs985700474","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611069,"source":"dbSNP","strand":1,"feature_type":"variation","end":140611069,"alleles":["G","A","T"],"seq_region_name":"7","id":"rs1799879489","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799879662","clinical_significance":[],"strand":1,"feature_type":"variation","end":140611070,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611070,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611071,"source":"dbSNP","strand":1,"feature_type":"variation","end":140611071,"alleles":["G","A"],"id":"rs987995585","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140611077,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611077,"clinical_significance":[],"seq_region_name":"7","id":"rs915115963"},{"clinical_significance":[],"id":"rs1246397806","seq_region_name":"7","end":140611080,"alleles":["CC","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140611079,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs921110878","seq_region_name":"7","feature_type":"variation","strand":1,"end":140611080,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611080},{"seq_region_name":"7","id":"rs1473394441","clinical_significance":[],"alleles":["T","C"],"end":140611081,"strand":1,"feature_type":"variation","start":140611081,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611082,"feature_type":"variation","strand":1,"end":140611082,"alleles":["G","A","C","T"],"clinical_significance":[],"id":"rs1208211068","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611085,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140611085,"seq_region_name":"7","id":"rs1324322648","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799880492","clinical_significance":[],"strand":1,"feature_type":"variation","end":140611086,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611086,"source":"dbSNP"},{"alleles":["C","T"],"end":140611087,"strand":1,"feature_type":"variation","start":140611087,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1799880599","seq_region_name":"7","clinical_significance":[]},{"id":"rs1799880702","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140611088,"strand":1,"feature_type":"variation","start":140611088,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799880853","source":"dbSNP","start":140611089,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140611089,"alleles":["A","C","G"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140611095,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611095,"source":"dbSNP","seq_region_name":"7","id":"rs1799880986","clinical_significance":[]},{"alleles":["G","A"],"end":140611097,"strand":1,"feature_type":"variation","start":140611097,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1161783123","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1217918575","seq_region_name":"7","alleles":["C","A"],"end":140611100,"feature_type":"variation","strand":1,"source":"dbSNP","start":140611100,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs947178327","seq_region_name":"7","clinical_significance":[],"start":140611102,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140611102,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"alleles":["G","A"],"end":140611105,"strand":1,"feature_type":"variation","start":140611105,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1799881534","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1344910538","feature_type":"variation","strand":1,"end":140611106,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611106},{"alleles":["T","C"],"end":140611108,"feature_type":"variation","strand":1,"source":"dbSNP","start":140611108,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1271206384"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611112,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140611112,"clinical_significance":[],"seq_region_name":"7","id":"rs1799881977"},{"clinical_significance":[],"id":"rs968766924","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140611114,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611114},{"end":140611115,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140611115,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799882250"},{"seq_region_name":"7","id":"rs373366854","clinical_significance":[],"start":140611122,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G","T"],"end":140611122,"strand":1,"feature_type":"variation"},{"end":140611123,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140611123,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1318069462","seq_region_name":"7"},{"id":"rs1585752560","seq_region_name":"7","clinical_significance":[],"start":140611126,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140611126,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140611127,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611127,"source":"dbSNP","seq_region_name":"7","id":"rs750098648","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1402112902","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611130,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140611130},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585752588","feature_type":"variation","strand":1,"end":140611131,"alleles":["A","C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611131},{"feature_type":"variation","strand":1,"end":140611132,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611132,"clinical_significance":[],"seq_region_name":"7","id":"rs1177946571"},{"seq_region_name":"7","id":"rs1400509214","clinical_significance":[],"strand":1,"feature_type":"variation","end":140611136,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611136,"source":"dbSNP"},{"end":140611138,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140611138,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799883211"},{"alleles":["T","G"],"end":140611141,"feature_type":"variation","strand":1,"source":"dbSNP","start":140611141,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585752612"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1324711482","source":"dbSNP","start":140611142,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140611142,"alleles":["T","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585752642","end":140611144,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140611144,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1424331828","alleles":["A","C"],"end":140611145,"feature_type":"variation","strand":1,"source":"dbSNP","start":140611145,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs934678130","feature_type":"variation","strand":1,"alleles":["C","A","G","T"],"end":140611147,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611147},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140611148,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611148,"source":"dbSNP","id":"rs542729109","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1057354600","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611155,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140611155},{"clinical_significance":[],"id":"rs6949464","seq_region_name":"7","end":140611169,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140611169,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563177561","alleles":["T","C"],"end":140611170,"feature_type":"variation","strand":1,"source":"dbSNP","start":140611170,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs894074781","source":"dbSNP","start":140611173,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140611173,"feature_type":"variation","strand":1},{"id":"rs528074895","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611174,"source":"dbSNP","strand":1,"feature_type":"variation","end":140611174,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1799884475","clinical_significance":[],"start":140611175,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140611175,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1799884546","clinical_significance":[],"end":140611177,"alleles":["GGG","GG"],"strand":1,"feature_type":"variation","start":140611175,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2908238","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611176,"feature_type":"variation","strand":1,"end":140611176,"alleles":["G","A"]},{"strand":1,"feature_type":"variation","end":140611177,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611177,"source":"dbSNP","seq_region_name":"7","id":"rs1042562707","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611179,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140611179,"seq_region_name":"7","id":"rs564994768","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799885075","clinical_significance":[],"end":140611181,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140611181,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140611182,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140611182,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs998606519"},{"clinical_significance":[],"id":"rs1799885264","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611183,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140611183},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611185,"source":"dbSNP","strand":1,"feature_type":"variation","end":140611185,"alleles":["G","T"],"seq_region_name":"7","id":"rs1216714377","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1340433217","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140611187,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611187},{"id":"rs888649971","seq_region_name":"7","clinical_significance":[],"alleles":["C","A","T"],"end":140611190,"strand":1,"feature_type":"variation","start":140611190,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140611191,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140611191,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs895462788"},{"alleles":["CCACCAC","CCAC"],"end":140611198,"feature_type":"variation","strand":1,"source":"dbSNP","start":140611192,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799885799"},{"feature_type":"variation","strand":1,"end":140611193,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611193,"clinical_significance":[],"seq_region_name":"7","id":"rs941075420"},{"seq_region_name":"7","id":"rs202231936","clinical_significance":[],"start":140611195,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140611195,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140611196,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611196,"clinical_significance":[],"seq_region_name":"7","id":"rs1036805015"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1304115886","source":"dbSNP","start":140611198,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140611198,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611200,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140611200,"seq_region_name":"7","id":"rs2130703797","clinical_significance":[]},{"source":"dbSNP","start":140611201,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140611201,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1799886293","seq_region_name":"7"},{"id":"rs2130703807","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611202,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140611202},{"seq_region_name":"7","id":"rs939677641","clinical_significance":[],"start":140611207,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140611219,"alleles":["TCTCTTTAAATCT","TCT"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140611209,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TCTTTAAATCTT","TCTT"],"end":140611220,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1358525172"},{"seq_region_name":"7","id":"rs1799886500","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140611210,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611210,"source":"dbSNP"},{"start":140611215,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140611215,"alleles":["A","C"],"strand":1,"feature_type":"variation","id":"rs1799886599","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799886695","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140611216,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611216},{"alleles":["G","T"],"end":140611228,"feature_type":"variation","strand":1,"source":"dbSNP","start":140611228,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799886776","seq_region_name":"7"},{"end":140611230,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140611230,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799886878"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1228676223","end":140611231,"alleles":["G","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140611231,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1291931313","source":"dbSNP","start":140611232,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140611232,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["TTT","TTTT"],"end":140611237,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611235,"source":"dbSNP","id":"rs1431402785","seq_region_name":"7","clinical_significance":[]},{"id":"rs765918369","seq_region_name":"7","clinical_significance":[],"end":140611250,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140611250,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["G","T"],"end":140611251,"strand":1,"feature_type":"variation","start":140611251,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799887456","clinical_significance":[]},{"source":"dbSNP","start":140611252,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140611252,"alleles":["C","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1445538663"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799887640","source":"dbSNP","start":140611254,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140611254,"alleles":["G","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs998267367","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611255,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140611255},{"clinical_significance":[],"seq_region_name":"7","id":"rs1029542308","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140611256,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611256},{"seq_region_name":"7","id":"rs889699803","clinical_significance":[],"start":140611257,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140611257,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140611258,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611258,"clinical_significance":[],"id":"rs1799887986","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611259,"feature_type":"variation","strand":1,"alleles":["C","-"],"end":140611259,"clinical_significance":[],"seq_region_name":"7","id":"rs553039289"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611264,"feature_type":"variation","strand":1,"end":140611264,"alleles":["G","A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799888193"},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140611269,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611269,"clinical_significance":[],"seq_region_name":"7","id":"rs1180242667"},{"alleles":["G","A"],"end":140611274,"feature_type":"variation","strand":1,"source":"dbSNP","start":140611274,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1026140911","seq_region_name":"7"},{"source":"dbSNP","start":140611278,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140611278,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1234001774"},{"start":140611286,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140611286,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799888595","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799888689","clinical_significance":[],"end":140611288,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140611288,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611289,"source":"dbSNP","strand":1,"feature_type":"variation","end":140611289,"alleles":["T","G"],"seq_region_name":"7","id":"rs924553731","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611290,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140611290,"seq_region_name":"7","id":"rs1207165002","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1482288526","end":140611295,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140611295,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130703940","feature_type":"variation","strand":1,"end":140611300,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611300},{"alleles":["T","G"],"end":140611310,"feature_type":"variation","strand":1,"source":"dbSNP","start":140611310,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1274452335"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611320,"feature_type":"variation","strand":1,"end":140611320,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799889155"},{"id":"rs761631366","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611326,"source":"dbSNP","strand":1,"feature_type":"variation","end":140611326,"alleles":["G","A","T"]},{"source":"dbSNP","start":140611332,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140611332,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1358412754"},{"seq_region_name":"7","id":"rs1799889472","clinical_significance":[],"start":140611335,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140611335,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611344,"source":"dbSNP","strand":1,"feature_type":"variation","end":140611344,"alleles":["C","T"],"seq_region_name":"7","id":"rs1799889581","clinical_significance":[]},{"source":"dbSNP","start":140611349,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140611349,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1006797583","seq_region_name":"7"},{"end":140611352,"alleles":["C","A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140611352,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs532337139","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799889905","feature_type":"variation","strand":1,"end":140611358,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611358},{"end":140611359,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140611359,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1179157963"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611360,"source":"dbSNP","strand":1,"feature_type":"variation","end":140611360,"alleles":["C","T"],"id":"rs1799890116","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1314369173","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140611361,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611361,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611366,"source":"dbSNP","strand":1,"feature_type":"variation","end":140611366,"alleles":["T","A","C"],"seq_region_name":"7","id":"rs1226148279","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799890481","source":"dbSNP","start":140611369,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140611369,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs950648673","feature_type":"variation","strand":1,"alleles":["AAAAAA","AAAAA"],"end":140611374,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611369},{"feature_type":"variation","strand":1,"end":140611388,"alleles":["AAAAAATAAAAAATAAAAAA","AAAAAATAAAAAA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611369,"clinical_significance":[],"seq_region_name":"7","id":"rs1411647620"},{"seq_region_name":"7","id":"rs1799890783","clinical_significance":[],"alleles":["A","G"],"end":140611370,"strand":1,"feature_type":"variation","start":140611370,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1799890883","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140611372,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611372,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1022073666","clinical_significance":[],"start":140611382,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140611382,"alleles":["T","A","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1469947405","clinical_significance":[],"start":140611383,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AAAAAAA","AAAAAA"],"end":140611389,"strand":1,"feature_type":"variation"},{"end":140611384,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140611384,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs550331450","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611385,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140611385,"seq_region_name":"7","id":"rs1799891342","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799891430","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611389,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140611389},{"seq_region_name":"7","id":"rs1387607892","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611394,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140611394},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799891641","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611397,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140611397},{"end":140611400,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140611400,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1307226652"},{"start":140611402,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140611402,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs1799891829","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130704083","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611406,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140611406},{"seq_region_name":"7","id":"rs1425041601","clinical_significance":[],"alleles":["G","A"],"end":140611408,"strand":1,"feature_type":"variation","start":140611408,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1351859978","alleles":["C","T"],"end":140611411,"feature_type":"variation","strand":1,"source":"dbSNP","start":140611411,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1162900197","seq_region_name":"7","clinical_significance":[],"start":140611418,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140611418,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs2130704107","clinical_significance":[],"start":140611419,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140611419,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130704112","end":140611424,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140611424,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799892733","source":"dbSNP","start":140611425,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140611425,"alleles":["G","C"],"feature_type":"variation","strand":1},{"id":"rs1799892815","seq_region_name":"7","clinical_significance":[],"start":140611426,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","-"],"end":140611426,"strand":1,"feature_type":"variation"},{"end":140611427,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140611427,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799892981","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1423339917","end":140611429,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140611429,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140611430,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140611430,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs912006983","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799893474","source":"dbSNP","start":140611431,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140611431,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs978794556","seq_region_name":"7","source":"dbSNP","start":140611433,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140611433,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs964654257","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611437,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140611437},{"seq_region_name":"7","id":"rs11767550","clinical_significance":[],"start":140611438,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140611438,"alleles":["C","G","T"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611441,"feature_type":"variation","strand":1,"alleles":["A","-"],"end":140611441,"clinical_significance":[],"id":"rs1266848187","seq_region_name":"7"},{"clinical_significance":[],"id":"rs915454451","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140611442,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611442},{"clinical_significance":[],"seq_region_name":"7","id":"rs956029119","feature_type":"variation","strand":1,"alleles":["G","A","C","T"],"end":140611443,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611443},{"alleles":["G","A"],"end":140611444,"feature_type":"variation","strand":1,"source":"dbSNP","start":140611444,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs993238381"},{"seq_region_name":"7","id":"rs1585753157","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140611449,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611449,"source":"dbSNP"},{"source":"dbSNP","start":140611450,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140611450,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799895173"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1229666482","source":"dbSNP","start":140611453,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140611453,"feature_type":"variation","strand":1},{"start":140611458,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140611458,"alleles":["A","G"],"strand":1,"feature_type":"variation","id":"rs1799895470","seq_region_name":"7","clinical_significance":[]},{"end":140611459,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140611459,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1411752737"},{"feature_type":"variation","strand":1,"end":140611460,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611460,"clinical_significance":[],"seq_region_name":"7","id":"rs1799895683"},{"strand":1,"feature_type":"variation","end":140611463,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611463,"source":"dbSNP","seq_region_name":"7","id":"rs1799895809","clinical_significance":[]},{"id":"rs1799895919","seq_region_name":"7","clinical_significance":[],"start":140611464,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140611464,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799896016","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611465,"feature_type":"variation","strand":1,"end":140611465,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1287596380","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611468,"source":"dbSNP","strand":1,"feature_type":"variation","end":140611468,"alleles":["G","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585753181","end":140611469,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140611469,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["T","C"],"end":140611470,"strand":1,"feature_type":"variation","start":140611470,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799896316","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799896418","clinical_significance":[],"end":140611474,"alleles":["GAGG","G"],"strand":1,"feature_type":"variation","start":140611471,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1799896519","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611475,"source":"dbSNP","strand":1,"feature_type":"variation","end":140611475,"alleles":["C","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563177687","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140611478,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611478},{"strand":1,"feature_type":"variation","end":140611481,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611481,"source":"dbSNP","id":"rs1327021616","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799896829","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140611483,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611483,"source":"dbSNP"},{"alleles":["G","T"],"end":140611484,"strand":1,"feature_type":"variation","start":140611484,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1799896919","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611485,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140611485,"clinical_significance":[],"id":"rs1335467353","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611488,"source":"dbSNP","strand":1,"feature_type":"variation","end":140611488,"alleles":["T","C"],"id":"rs1799897129","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799897203","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611489,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140611489},{"start":140611492,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140611492,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585753223","clinical_significance":[]},{"clinical_significance":[],"id":"rs1369381823","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611493,"feature_type":"variation","strand":1,"alleles":["GCATCA","GCATCAAGGCATCA"],"end":140611498},{"clinical_significance":[],"seq_region_name":"7","id":"rs1292019974","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611494,"feature_type":"variation","strand":1,"end":140611494,"alleles":["C","A","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799897625","source":"dbSNP","start":140611495,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140611495,"feature_type":"variation","strand":1},{"alleles":["C","G"],"end":140611497,"strand":1,"feature_type":"variation","start":140611497,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1799897719","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140611501,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140611501,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1436107514","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585753257","source":"dbSNP","start":140611503,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C","T"],"end":140611503,"feature_type":"variation","strand":1},{"start":140611508,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140611508,"strand":1,"feature_type":"variation","id":"rs866238989","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799898120","end":140611509,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140611509,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs917294194","clinical_significance":[],"alleles":["C","T"],"end":140611510,"strand":1,"feature_type":"variation","start":140611510,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1455662265","source":"dbSNP","start":140611512,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140611512,"alleles":["T","TTGTT"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs948975942","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140611514,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611514},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611516,"source":"dbSNP","strand":1,"feature_type":"variation","end":140611516,"alleles":["C","A"],"seq_region_name":"7","id":"rs9691338","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140611523,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611523,"clinical_significance":[],"seq_region_name":"7","id":"rs1799898632"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1177696334","feature_type":"variation","strand":1,"end":140611524,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611524},{"clinical_significance":[],"seq_region_name":"7","id":"rs1435288116","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611525,"feature_type":"variation","strand":1,"end":140611525,"alleles":["G","A","T"]},{"strand":1,"feature_type":"variation","end":140611529,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611529,"source":"dbSNP","id":"rs548255304","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611535,"source":"dbSNP","strand":1,"feature_type":"variation","end":140611535,"alleles":["C","G"],"seq_region_name":"7","id":"rs866703958","clinical_significance":[]},{"id":"rs1799899185","seq_region_name":"7","clinical_significance":[],"end":140611544,"alleles":["AAAATAA","AAAATAATAAATACATAAATATATAAATAAATATATAAATACATAAATATAAAAATATTTAATATTTTTATTAATTAAAATTAATTAAAATATTAAAAATATATAAATAAATATATAAATACATAAATATAAAAATAA"],"strand":1,"feature_type":"variation","start":140611538,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1190973113","clinical_significance":[],"start":140611543,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140611545,"alleles":["AAA","AA"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1487977573","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611546,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","TT"],"end":140611546},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140611547,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611547,"clinical_significance":[],"seq_region_name":"7","id":"rs182189490"},{"clinical_significance":[],"id":"rs1799899576","seq_region_name":"7","end":140611550,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140611550,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1799899668","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140611552,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611552},{"end":140611553,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140611553,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1210079984","clinical_significance":[]},{"source":"dbSNP","start":140611556,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140611556,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs781402920"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1267437512","alleles":["A","G"],"end":140611557,"feature_type":"variation","strand":1,"source":"dbSNP","start":140611557,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140611560,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140611560,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1223984292","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1275284467","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611568,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140611568},{"clinical_significance":[],"id":"rs1799900254","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611578,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140611578},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611579,"source":"dbSNP","strand":1,"feature_type":"variation","end":140611579,"alleles":["G","A"],"seq_region_name":"7","id":"rs533930901","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611580,"feature_type":"variation","strand":1,"end":140611581,"alleles":["TT","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799900437"},{"strand":1,"feature_type":"variation","end":140611584,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611584,"source":"dbSNP","id":"rs1299014722","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611587,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140611587,"seq_region_name":"7","id":"rs1385986226","clinical_significance":[]},{"seq_region_name":"7","id":"rs1193646222","clinical_significance":[],"start":140611592,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140611592,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140611593,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611593,"source":"dbSNP","id":"rs1799900965","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140611597,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611597,"clinical_significance":[],"id":"rs187158792","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611602,"source":"dbSNP","strand":1,"feature_type":"variation","end":140611602,"alleles":["A","G"],"seq_region_name":"7","id":"rs1442692344","clinical_significance":[]},{"alleles":["G","C"],"end":140611605,"feature_type":"variation","strand":1,"source":"dbSNP","start":140611605,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1362942833","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140611607,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611607,"source":"dbSNP","seq_region_name":"7","id":"rs1799901478","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611611,"source":"dbSNP","strand":1,"feature_type":"variation","end":140611611,"alleles":["T","C"],"id":"rs933796366","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140611612,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611612,"clinical_significance":[],"id":"rs1799901586","seq_region_name":"7"},{"source":"dbSNP","start":140611617,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140611617,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130704455"},{"id":"rs1051195168","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140611619,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611619,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799901790","clinical_significance":[],"start":140611620,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AA","A"],"end":140611621,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140611622,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611622,"clinical_significance":[],"seq_region_name":"7","id":"rs80275524"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1006745460","alleles":["T","G"],"end":140611628,"feature_type":"variation","strand":1,"source":"dbSNP","start":140611628,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140611636,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140611636,"alleles":["A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130704486","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140611640,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611640,"clinical_significance":[],"seq_region_name":"7","id":"rs1022188536"},{"strand":1,"feature_type":"variation","end":140611643,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611643,"source":"dbSNP","seq_region_name":"7","id":"rs748561704","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140611644,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611644,"clinical_significance":[],"seq_region_name":"7","id":"rs1337452110"},{"clinical_significance":[],"seq_region_name":"7","id":"rs144634732","feature_type":"variation","strand":1,"end":140611646,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611646},{"end":140611649,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140611649,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1376396662"},{"clinical_significance":[],"id":"rs1031714067","seq_region_name":"7","source":"dbSNP","start":140611653,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140611653,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs192452586","feature_type":"variation","strand":1,"end":140611654,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611654},{"seq_region_name":"7","id":"rs2130704521","clinical_significance":[],"start":140611662,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140611662,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140611664,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611664,"clinical_significance":[],"seq_region_name":"7","id":"rs1390439731"},{"id":"rs1799902852","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611670,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140611670},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799902951","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611671,"feature_type":"variation","strand":1,"end":140611671,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1799903051","clinical_significance":[],"start":140611674,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140611674,"alleles":["T","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1585753554","clinical_significance":[],"start":140611690,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140611690,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1463586091","clinical_significance":[],"start":140611694,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140611694,"alleles":["C","A","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1166284804","source":"dbSNP","start":140611695,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140611695,"alleles":["A","G"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611697,"feature_type":"variation","strand":1,"end":140611704,"alleles":["GAAGGAAG","GAAG"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799903451"},{"strand":1,"feature_type":"variation","end":140611699,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611699,"source":"dbSNP","seq_region_name":"7","id":"rs1799903547","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611700,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140611700,"id":"rs1799903647","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140611702,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611702,"source":"dbSNP","id":"rs1799903749","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140611705,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140611705,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799903849"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611707,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140611707,"seq_region_name":"7","id":"rs1799903954","clinical_significance":[]},{"alleles":["G","C"],"end":140611717,"strand":1,"feature_type":"variation","start":140611717,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1799904036","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799904138","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611722,"source":"dbSNP","strand":1,"feature_type":"variation","end":140611722,"alleles":["C","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611723,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140611723,"clinical_significance":[],"id":"rs992959562","seq_region_name":"7"},{"alleles":["A","G"],"end":140611725,"strand":1,"feature_type":"variation","start":140611725,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1338693156","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799904400","clinical_significance":[],"alleles":["T","C","G"],"end":140611726,"strand":1,"feature_type":"variation","start":140611726,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1799904502","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140611728,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611728,"source":"dbSNP"},{"source":"dbSNP","start":140611730,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140611730,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799904642"},{"seq_region_name":"7","id":"rs1799904923","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611733,"source":"dbSNP","strand":1,"feature_type":"variation","end":140611733,"alleles":["A","G"]},{"alleles":["T","G"],"end":140611741,"strand":1,"feature_type":"variation","start":140611741,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1024713143","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611743,"feature_type":"variation","strand":1,"end":140611743,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799905162"},{"source":"dbSNP","start":140611745,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140611745,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130704632"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799905263","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611750,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140611750},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611754,"feature_type":"variation","strand":1,"end":140611754,"alleles":["C","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs78225769"},{"seq_region_name":"7","id":"rs147476447","clinical_significance":[],"strand":1,"feature_type":"variation","end":140611759,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611759,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611760,"feature_type":"variation","strand":1,"end":140611760,"alleles":["G","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1232296489"},{"seq_region_name":"7","id":"rs910149668","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611762,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140611762},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611763,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140611763,"seq_region_name":"7","id":"rs377753101","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611764,"feature_type":"variation","strand":1,"end":140611764,"alleles":["A","C"],"clinical_significance":[],"id":"rs1300110518","seq_region_name":"7"},{"source":"dbSNP","start":140611769,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140611772,"alleles":["CACA","CA"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799905987"},{"start":140611773,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140611773,"alleles":["G","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799906080","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs369176809","feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140611775,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611775},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140611776,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611776,"source":"dbSNP","seq_region_name":"7","id":"rs1799906301","clinical_significance":[]},{"seq_region_name":"7","id":"rs1226539074","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611777,"source":"dbSNP","strand":1,"feature_type":"variation","end":140611777,"alleles":["C","T"]},{"alleles":["G","A"],"end":140611778,"feature_type":"variation","strand":1,"source":"dbSNP","start":140611778,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs972893673","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799906602","clinical_significance":[],"strand":1,"feature_type":"variation","end":140611779,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611779,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799906684","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611780,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140611780},{"alleles":["G","C","T"],"end":140611782,"feature_type":"variation","strand":1,"source":"dbSNP","start":140611782,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799906779"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1315870667","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611785,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140611785},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799907045","source":"dbSNP","start":140611788,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140611788,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1397837080","source":"dbSNP","start":140611790,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140611790,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611796,"feature_type":"variation","strand":1,"end":140611796,"alleles":["T","A","C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1400721245"},{"id":"rs1799907387","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","-"],"end":140611800,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611800,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611800,"feature_type":"variation","strand":1,"end":140611800,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130704735"},{"end":140611802,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140611802,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs918795801","clinical_significance":[]},{"id":"rs1799907575","seq_region_name":"7","clinical_significance":[],"end":140611804,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140611804,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611805,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140611805,"id":"rs1799907674","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs933721941","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611807,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140611807},{"strand":1,"feature_type":"variation","end":140611809,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611809,"source":"dbSNP","seq_region_name":"7","id":"rs1451656729","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799907971","clinical_significance":[],"end":140611811,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140611811,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1050886907","end":140611820,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140611820,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140611822,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611822,"clinical_significance":[],"seq_region_name":"7","id":"rs749529655"},{"seq_region_name":"7","id":"rs1563177816","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140611823,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611823,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1585753737","seq_region_name":"7","source":"dbSNP","start":140611825,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140611825,"feature_type":"variation","strand":1},{"id":"rs1298241029","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611828,"source":"dbSNP","strand":1,"feature_type":"variation","end":140611828,"alleles":["C","A","T"]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140611829,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611829,"source":"dbSNP","id":"rs974680556","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1585753773","seq_region_name":"7","source":"dbSNP","start":140611834,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140611834,"alleles":["T","C"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611836,"feature_type":"variation","strand":1,"end":140611836,"alleles":["T","C"],"clinical_significance":[],"id":"rs1799909823","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1167089174","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140611839,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611839,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs915233407","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611841,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140611841},{"seq_region_name":"7","id":"rs968491512","clinical_significance":[],"start":140611842,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140611842,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs139308183","clinical_significance":[],"end":140611843,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140611843,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs539800232","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611844,"source":"dbSNP","strand":1,"feature_type":"variation","end":140611844,"alleles":["T","A"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611845,"feature_type":"variation","strand":1,"end":140611845,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1253998550"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1250310348","alleles":["G","A"],"end":140611847,"feature_type":"variation","strand":1,"source":"dbSNP","start":140611847,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140611861,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140611861,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1345148851"},{"seq_region_name":"7","id":"rs180794505","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611863,"source":"dbSNP","strand":1,"feature_type":"variation","end":140611863,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs942381086","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611864,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140611864},{"clinical_significance":[],"id":"rs150025431","seq_region_name":"7","feature_type":"variation","strand":1,"end":140611868,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611868},{"clinical_significance":[],"seq_region_name":"7","id":"rs376466165","feature_type":"variation","strand":1,"end":140611869,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611869},{"seq_region_name":"7","id":"rs1315938340","clinical_significance":[],"start":140611871,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140611871,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1799910868","clinical_significance":[],"end":140611881,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140611881,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611884,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140611884,"seq_region_name":"7","id":"rs1799911039","clinical_significance":[]},{"end":140611888,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140611888,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs562367716","clinical_significance":[]},{"alleles":["G","A"],"end":140611889,"feature_type":"variation","strand":1,"source":"dbSNP","start":140611889,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs770860860"},{"start":140611893,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140611893,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs529836734","clinical_significance":[]},{"clinical_significance":[],"id":"rs2130704904","seq_region_name":"7","source":"dbSNP","start":140611897,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140611897,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799911703","end":140611899,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140611899,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140611900,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140611900,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs1799911852","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140611903,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611903,"source":"dbSNP","seq_region_name":"7","id":"rs1799912005","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799912175","clinical_significance":[],"end":140611905,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140611905,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs896350075","clinical_significance":[],"start":140611907,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140611907,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1044208927","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611908,"feature_type":"variation","strand":1,"end":140611908,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1799912537","clinical_significance":[],"start":140611911,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140611911,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"id":"rs1799912642","seq_region_name":"7","clinical_significance":[],"start":140611913,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140611913,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"start":140611921,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140611921,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1056756921","clinical_significance":[]},{"id":"rs1306613625","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140611924,"strand":1,"feature_type":"variation","start":140611924,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["C","T"],"end":140611928,"strand":1,"feature_type":"variation","start":140611928,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130704968","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611929,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140611929,"clinical_significance":[],"seq_region_name":"7","id":"rs1799912936"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140611934,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611934,"source":"dbSNP","seq_region_name":"7","id":"rs548315791","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611936,"feature_type":"variation","strand":1,"end":140611936,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1372533155"},{"end":140611943,"alleles":["TACAGTTT","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140611936,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1369589245","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611938,"source":"dbSNP","strand":1,"feature_type":"variation","end":140611938,"alleles":["C","-"],"id":"rs1163408850","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs145376498","feature_type":"variation","strand":1,"end":140611939,"alleles":["A","C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611939},{"source":"dbSNP","start":140611948,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140611948,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799914045"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799914182","feature_type":"variation","strand":1,"end":140611950,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611950},{"seq_region_name":"7","id":"rs1799914325","clinical_significance":[],"end":140611954,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","start":140611954,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1178775638","clinical_significance":[],"end":140611955,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140611955,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611957,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140611957,"id":"rs115152338","seq_region_name":"7","clinical_significance":[]},{"alleles":["TT","T"],"end":140611958,"feature_type":"variation","strand":1,"source":"dbSNP","start":140611957,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799914936"},{"end":140611958,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140611958,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1799915132","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140611959,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140611959,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs970018082"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1472900160","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611960,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140611960},{"feature_type":"variation","strand":1,"end":140611966,"alleles":["T","A","C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611966,"clinical_significance":[],"id":"rs774551689","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1001543729","clinical_significance":[],"start":140611968,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140611968,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["G","A","C","T"],"end":140611969,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611969,"source":"dbSNP","seq_region_name":"7","id":"rs994941869","clinical_significance":[]},{"alleles":["G","A","C"],"end":140611973,"strand":1,"feature_type":"variation","start":140611973,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1016985954","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs7811087","source":"dbSNP","start":140611978,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140611978,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1321040295","end":140611979,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140611979,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611980,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140611980,"seq_region_name":"7","id":"rs1799916379","clinical_significance":[]},{"start":140611981,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140611981,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130705105","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611982,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140611982,"seq_region_name":"7","id":"rs1563177904","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611983,"source":"dbSNP","strand":1,"feature_type":"variation","end":140611983,"alleles":["G","C"],"id":"rs973037197","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1265009961","alleles":["T","C"],"end":140611984,"feature_type":"variation","strand":1,"source":"dbSNP","start":140611984,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs918731679","clinical_significance":[],"strand":1,"feature_type":"variation","end":140611985,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611985,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799916836","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140611988,"feature_type":"variation","strand":1,"end":140611988,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs570810104","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140611994,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140611994,"source":"dbSNP"},{"alleles":["T","C"],"end":140611997,"feature_type":"variation","strand":1,"source":"dbSNP","start":140611997,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1229054403"},{"seq_region_name":"7","id":"rs1439175630","clinical_significance":[],"end":140611998,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140611998,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1799917267","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612003,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140612003},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799917370","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140612007,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612007},{"source":"dbSNP","start":140612010,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140612010,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1331909887"},{"clinical_significance":[],"id":"rs1585754170","seq_region_name":"7","end":140612015,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140612015,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1799917677","seq_region_name":"7","end":140612018,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140612018,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140612021,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612021,"clinical_significance":[],"seq_region_name":"7","id":"rs1799917768"},{"seq_region_name":"7","id":"rs955584273","clinical_significance":[],"start":140612028,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140612028,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612029,"source":"dbSNP","strand":1,"feature_type":"variation","end":140612029,"alleles":["T","G"],"seq_region_name":"7","id":"rs1585754183","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612031,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140612031,"id":"rs2130705192","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1409600900","end":140612033,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140612033,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140612035,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140612035,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1387008554","clinical_significance":[]},{"seq_region_name":"7","id":"rs538567438","clinical_significance":[],"alleles":["C","T"],"end":140612038,"strand":1,"feature_type":"variation","start":140612038,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140612039,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612039,"clinical_significance":[],"seq_region_name":"7","id":"rs556893700"},{"seq_region_name":"7","id":"rs1585754232","clinical_significance":[],"alleles":["G","A","T"],"end":140612041,"strand":1,"feature_type":"variation","start":140612041,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799918655","source":"dbSNP","start":140612043,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140612043,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140612044,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612044,"clinical_significance":[],"seq_region_name":"7","id":"rs1799918763"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612046,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140612046,"seq_region_name":"7","id":"rs2130705226","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799918877","clinical_significance":[],"strand":1,"feature_type":"variation","end":140612047,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612047,"source":"dbSNP"},{"seq_region_name":"7","id":"rs2130705237","clinical_significance":[],"start":140612050,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140612050,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs986924888","seq_region_name":"7","alleles":["A","C"],"end":140612051,"feature_type":"variation","strand":1,"source":"dbSNP","start":140612051,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140612058,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612058,"source":"dbSNP","seq_region_name":"7","id":"rs1585754250","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs765292955","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140612060,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612060},{"start":140612064,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140612064,"alleles":["A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585754271","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140612065,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612065,"clinical_significance":[],"seq_region_name":"7","id":"rs1799919377"},{"strand":1,"feature_type":"variation","end":140612068,"alleles":["CCCC","CCC"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612065,"source":"dbSNP","seq_region_name":"7","id":"rs1388217558","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799919580","clinical_significance":[],"alleles":["C","T"],"end":140612066,"strand":1,"feature_type":"variation","start":140612066,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["C","T"],"end":140612068,"strand":1,"feature_type":"variation","start":140612068,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs568713903","clinical_significance":[]},{"source":"dbSNP","start":140612069,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140612069,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs942333655"},{"start":140612070,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140612070,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1457264587","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1043373705","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612073,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140612073},{"start":140612075,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140612075,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1472150975","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585754321","clinical_significance":[],"start":140612076,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","T"],"end":140612076,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130705301","source":"dbSNP","start":140612086,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140612091,"alleles":["AAAAAA","AAAAAAA"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1008646211","feature_type":"variation","strand":1,"end":140612087,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612087},{"seq_region_name":"7","id":"rs1280967072","clinical_significance":[],"alleles":["A","C"],"end":140612089,"strand":1,"feature_type":"variation","start":140612089,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612091,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140612091,"seq_region_name":"7","id":"rs1799920581","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799920690","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612097,"source":"dbSNP","strand":1,"feature_type":"variation","end":140612097,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1200730707","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140612098,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612098,"source":"dbSNP"},{"alleles":["G","A"],"end":140612100,"strand":1,"feature_type":"variation","start":140612100,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1450130270","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140612102,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612102,"clinical_significance":[],"id":"rs553877902","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140612104,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612104,"clinical_significance":[],"seq_region_name":"7","id":"rs1563177948"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612106,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140612106,"seq_region_name":"7","id":"rs1799921362","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140612112,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612112,"source":"dbSNP","seq_region_name":"7","id":"rs924985845","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799921556","clinical_significance":[],"alleles":["T","C"],"end":140612113,"strand":1,"feature_type":"variation","start":140612113,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1799921652","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140612114,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612114,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140612115,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612115,"clinical_significance":[],"id":"rs1799921766","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1018741048","seq_region_name":"7","source":"dbSNP","start":140612118,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140612118,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs900377372","clinical_significance":[],"start":140612119,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140612119,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140612127,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140612127,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799922103"},{"source":"dbSNP","start":140612132,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140612132,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1223257981"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1228380719","end":140612136,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140612136,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1346319993","end":140612139,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140612139,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140612140,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612140,"source":"dbSNP","seq_region_name":"7","id":"rs536018700","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612149,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140612149,"clinical_significance":[],"seq_region_name":"7","id":"rs1022823267"},{"source":"dbSNP","start":140612151,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C","G"],"end":140612151,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1052388153"},{"seq_region_name":"7","id":"rs1329017662","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140612152,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612152,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1487070144","end":140612155,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140612155,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs776388788","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","C","T"],"end":140612156,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612156,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612158,"source":"dbSNP","strand":1,"feature_type":"variation","end":140612158,"alleles":["T","C"],"seq_region_name":"7","id":"rs1435194049","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799923342","clinical_significance":[],"strand":1,"feature_type":"variation","end":140612165,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612165,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799923442","source":"dbSNP","start":140612166,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140612168,"alleles":["GGG","GG"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612172,"source":"dbSNP","strand":1,"feature_type":"variation","end":140612172,"alleles":["C","T"],"seq_region_name":"7","id":"rs1013433437","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799923620","seq_region_name":"7","source":"dbSNP","start":140612173,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140612173,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1799923721","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612181,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140612181},{"alleles":["A","C"],"end":140612186,"feature_type":"variation","strand":1,"source":"dbSNP","start":140612186,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs554654519"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612188,"feature_type":"variation","strand":1,"end":140612188,"alleles":["C","T"],"clinical_significance":[],"id":"rs796171984","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1425751736","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612190,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140612190},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799924112","feature_type":"variation","strand":1,"end":140612193,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612193},{"strand":1,"feature_type":"variation","end":140612194,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612194,"source":"dbSNP","seq_region_name":"7","id":"rs905944717","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140612196,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612196,"clinical_significance":[],"id":"rs978508627","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140612197,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612197,"source":"dbSNP","seq_region_name":"7","id":"rs1377284617","clinical_significance":[]},{"seq_region_name":"7","id":"rs1001653299","clinical_significance":[],"end":140612198,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140612198,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["A","G"],"end":140612201,"feature_type":"variation","strand":1,"source":"dbSNP","start":140612201,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1201759942","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1016932171","source":"dbSNP","start":140612203,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140612203,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1480257566","clinical_significance":[],"alleles":["G","A"],"end":140612204,"strand":1,"feature_type":"variation","start":140612204,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140612205,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140612205,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs992446652"},{"end":140612206,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140612206,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1585754637","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799925077","source":"dbSNP","start":140612207,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140612207,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612212,"source":"dbSNP","strand":1,"feature_type":"variation","end":140612212,"alleles":["G","A"],"seq_region_name":"7","id":"rs962727099","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140612214,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612214,"source":"dbSNP","seq_region_name":"7","id":"rs572255290","clinical_significance":[]},{"source":"dbSNP","start":140612216,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140612216,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs994801933","seq_region_name":"7"},{"start":140612222,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140612222,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799925455","clinical_significance":[]},{"start":140612223,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140612223,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1281282809","clinical_significance":[]},{"clinical_significance":[],"id":"rs868518074","seq_region_name":"7","source":"dbSNP","start":140612227,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140612227,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1585754675","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140612228,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612228,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140612235,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612235,"clinical_significance":[],"seq_region_name":"7","id":"rs948226796"},{"id":"rs1799926014","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140612240,"alleles":["CGTCTC","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612235,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs955691642","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140612236,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612236},{"start":140612240,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140612240,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799926309","clinical_significance":[]},{"source":"dbSNP","start":140612243,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140612243,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs80181641"},{"start":140612244,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140612251,"alleles":["AAAAAAAA","AAAAAAA","AAAAAAAAA"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs979836741","clinical_significance":[]},{"start":140612245,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140612245,"alleles":["A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs986987430","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140612247,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612247,"source":"dbSNP","seq_region_name":"7","id":"rs1799926860","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["AG","-"],"end":140612252,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612251,"source":"dbSNP","seq_region_name":"7","id":"rs1799926949","clinical_significance":[]},{"alleles":["-","AG"],"end":140612251,"feature_type":"variation","strand":1,"source":"dbSNP","start":140612252,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799927046"},{"alleles":["G","A"],"end":140612252,"strand":1,"feature_type":"variation","start":140612252,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1288150725","clinical_significance":[]},{"clinical_significance":[],"id":"rs1451378730","seq_region_name":"7","feature_type":"variation","strand":1,"end":140612253,"alleles":["GG","GGG"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612252},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799927321","feature_type":"variation","strand":1,"alleles":["-","A"],"end":140612252,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612253},{"clinical_significance":[],"id":"rs111703115","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612253,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140612253},{"clinical_significance":[],"seq_region_name":"7","id":"rs542011993","source":"dbSNP","start":140612254,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140612265,"alleles":["AAAAAAAAAAAA","AAAAAAAAAAA","AAAAAAAAAAAAA","AAAAAAAAAAAAAA"],"feature_type":"variation","strand":1},{"end":140612258,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140612258,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1391443696","clinical_significance":[]},{"end":140612263,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140612263,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1799927800","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs911432727","source":"dbSNP","start":140612264,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140612264,"alleles":["A","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs35661058","seq_region_name":"7","alleles":["-","G"],"end":140612264,"feature_type":"variation","strand":1,"source":"dbSNP","start":140612265,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["A","G"],"end":140612265,"strand":1,"feature_type":"variation","start":140612265,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs74388150","clinical_significance":[]},{"clinical_significance":[],"id":"rs963759300","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612266,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140612266},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612267,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140612267,"clinical_significance":[],"id":"rs1585754831","seq_region_name":"7"},{"clinical_significance":[],"id":"rs761548756","seq_region_name":"7","feature_type":"variation","strand":1,"end":140612271,"alleles":["T","C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612271},{"seq_region_name":"7","id":"rs1799928477","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140612272,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612272,"source":"dbSNP"},{"end":140612276,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140612276,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1300798064","seq_region_name":"7","clinical_significance":[]},{"end":140612280,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140612280,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1344439146"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612282,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140612282,"clinical_significance":[],"seq_region_name":"7","id":"rs1228576888"},{"id":"rs1799928879","seq_region_name":"7","clinical_significance":[],"start":140612284,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140612284,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs6464904","source":"dbSNP","start":140612291,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140612291,"alleles":["T","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs930303663","end":140612303,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140612303,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140612304,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612304,"source":"dbSNP","seq_region_name":"7","id":"rs1799929313","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs924933479","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612306,"feature_type":"variation","strand":1,"end":140612306,"alleles":["A","G"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612314,"feature_type":"variation","strand":1,"end":140612314,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799929595"},{"clinical_significance":[],"seq_region_name":"7","id":"rs114330442","source":"dbSNP","start":140612321,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140612321,"alleles":["T","A","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1237426079","source":"dbSNP","start":140612322,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140612322,"alleles":["G","A","T"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140612329,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612329,"clinical_significance":[],"seq_region_name":"7","id":"rs1799929923"},{"start":140612330,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140612330,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs558300218","clinical_significance":[]},{"seq_region_name":"7","id":"rs536264011","clinical_significance":[],"start":140612331,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140612331,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1207733075","clinical_significance":[],"strand":1,"feature_type":"variation","end":140612332,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612332,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1343926945","clinical_significance":[],"strand":1,"feature_type":"variation","end":140612333,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612333,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1213478255","clinical_significance":[],"strand":1,"feature_type":"variation","end":140612340,"alleles":["AAAAAAA","AAAAAA","AAAAAAAA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612334,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612345,"feature_type":"variation","strand":1,"end":140612345,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs917849645"},{"start":140612345,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140612350,"alleles":["ATATAT","ATAT"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1379204915","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585754984","clinical_significance":[],"start":140612346,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140612346,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs949203417","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612352,"source":"dbSNP","strand":1,"feature_type":"variation","end":140612352,"alleles":["C","A","G","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612353,"source":"dbSNP","strand":1,"feature_type":"variation","end":140612353,"alleles":["G","A"],"seq_region_name":"7","id":"rs143930668","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585754998","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612355,"feature_type":"variation","strand":1,"end":140612355,"alleles":["A","C"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612357,"source":"dbSNP","strand":1,"feature_type":"variation","end":140612357,"alleles":["G","A"],"seq_region_name":"7","id":"rs1799931541","clinical_significance":[]},{"alleles":["G","C"],"end":140612362,"strand":1,"feature_type":"variation","start":140612362,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1308472806","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612364,"feature_type":"variation","strand":1,"end":140612364,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs905056035"},{"feature_type":"variation","strand":1,"end":140612366,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612366,"clinical_significance":[],"seq_region_name":"7","id":"rs1799931816"},{"id":"rs1799931914","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612369,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140612369},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799932006","source":"dbSNP","start":140612386,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140612386,"alleles":["A","G"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140612389,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140612389,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs866832025"},{"alleles":["A","G"],"end":140612403,"strand":1,"feature_type":"variation","start":140612403,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs937389622","seq_region_name":"7","clinical_significance":[]},{"end":140612405,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140612405,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1266814065","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1563178125","clinical_significance":[],"strand":1,"feature_type":"variation","end":140612407,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612407,"source":"dbSNP"},{"alleles":["C","T"],"end":140612409,"feature_type":"variation","strand":1,"source":"dbSNP","start":140612409,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1169962328","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799932746","feature_type":"variation","strand":1,"end":140612412,"alleles":["TTT","TT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612410},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799932907","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612418,"feature_type":"variation","strand":1,"end":140612418,"alleles":["T","C"]},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140612419,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612419,"source":"dbSNP","seq_region_name":"7","id":"rs1799933046","clinical_significance":[]},{"alleles":["T","C"],"end":140612425,"feature_type":"variation","strand":1,"source":"dbSNP","start":140612425,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799933188"},{"start":140612430,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140612430,"alleles":["T","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130705872","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612433,"feature_type":"variation","strand":1,"end":140612433,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1406049098"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612435,"source":"dbSNP","strand":1,"feature_type":"variation","end":140612435,"alleles":["T","C"],"seq_region_name":"7","id":"rs1799933330","clinical_significance":[]},{"end":140612444,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140612444,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1038480913"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612447,"source":"dbSNP","strand":1,"feature_type":"variation","end":140612447,"alleles":["A","G"],"seq_region_name":"7","id":"rs1180158962","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140612448,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612448,"source":"dbSNP","seq_region_name":"7","id":"rs1472795947","clinical_significance":[]},{"alleles":["AAGTAAA","AA"],"end":140612455,"feature_type":"variation","strand":1,"source":"dbSNP","start":140612449,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799934368"},{"id":"rs1253145288","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140612450,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612450,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs544146174","end":140612451,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140612451,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs994187083","source":"dbSNP","start":140612452,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140612452,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1799934979","seq_region_name":"7","source":"dbSNP","start":140612454,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140612454,"alleles":["A","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1799935145","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612456,"source":"dbSNP","strand":1,"feature_type":"variation","end":140612456,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1482237810","clinical_significance":[],"alleles":["T","G"],"end":140612463,"strand":1,"feature_type":"variation","start":140612463,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["T","C"],"end":140612465,"feature_type":"variation","strand":1,"source":"dbSNP","start":140612465,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs562433510","seq_region_name":"7"},{"id":"rs765047621","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612466,"source":"dbSNP","strand":1,"feature_type":"variation","end":140612466,"alleles":["A","G"]},{"start":140612467,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140612467,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs903952205","clinical_significance":[]},{"id":"rs1183097392","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140612469,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612469,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612469,"feature_type":"variation","strand":1,"alleles":["TAACTT","T"],"end":140612474,"clinical_significance":[],"seq_region_name":"7","id":"rs1799936043"},{"seq_region_name":"7","id":"rs999501172","clinical_significance":[],"start":140612472,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140612472,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612476,"source":"dbSNP","strand":1,"feature_type":"variation","end":140612476,"alleles":["A","G"],"seq_region_name":"7","id":"rs1799936318","clinical_significance":[]},{"seq_region_name":"7","id":"rs1291489915","clinical_significance":[],"alleles":["C","T"],"end":140612479,"strand":1,"feature_type":"variation","start":140612479,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140612486,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140612486,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1226105858"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612489,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140612489,"seq_region_name":"7","id":"rs1799936744","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799936893","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612493,"feature_type":"variation","strand":1,"end":140612493,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs891372360","source":"dbSNP","start":140612494,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140612494,"alleles":["T","C"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612495,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140612495,"clinical_significance":[],"seq_region_name":"7","id":"rs1008931485"},{"alleles":["G","A","C"],"end":140612496,"feature_type":"variation","strand":1,"source":"dbSNP","start":140612496,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1031415286"},{"seq_region_name":"7","id":"rs1018386667","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140612502,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612502,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612503,"feature_type":"variation","strand":1,"end":140612503,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1411462723"},{"seq_region_name":"7","id":"rs576223402","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["-","G"],"end":140612505,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612506,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585755277","feature_type":"variation","strand":1,"alleles":["T","A"],"end":140612506,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612506},{"id":"rs552346129","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140612519,"alleles":["TTTTTTTTTTTTTT","TTTTTTTTTTTT","TTTTTTTTTTTTT","TTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTATACTAATTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612506,"source":"dbSNP"},{"alleles":["T","A"],"end":140612512,"feature_type":"variation","strand":1,"source":"dbSNP","start":140612512,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs574299800"},{"source":"dbSNP","start":140612519,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140612519,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs79634309"},{"seq_region_name":"7","id":"rs77882229","clinical_significance":[],"start":140612520,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140612520,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"end":140612520,"alleles":["G","-"],"strand":1,"feature_type":"variation","start":140612520,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1413343850","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140612525,"alleles":["A","AA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612525,"source":"dbSNP","seq_region_name":"7","id":"rs1471886704","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799938498","clinical_significance":[],"start":140612525,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140612528,"alleles":["AGAG","AG"],"strand":1,"feature_type":"variation"},{"start":140612528,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140612528,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1023923295","clinical_significance":[]},{"seq_region_name":"7","id":"rs969517780","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612529,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TCTTA","TCTTATCTTA"],"end":140612533},{"feature_type":"variation","strand":1,"end":140612534,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612534,"clinical_significance":[],"seq_region_name":"7","id":"rs964206314"},{"seq_region_name":"7","id":"rs920319131","clinical_significance":[],"alleles":["G","A"],"end":140612541,"strand":1,"feature_type":"variation","start":140612541,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["C","T"],"end":140612543,"strand":1,"feature_type":"variation","start":140612543,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs930396525","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs541576302","feature_type":"variation","strand":1,"end":140612544,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612544},{"seq_region_name":"7","id":"rs1230204062","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612545,"source":"dbSNP","strand":1,"feature_type":"variation","end":140612545,"alleles":["G","A","C"]},{"start":140612548,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140612548,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130706083","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799939488","feature_type":"variation","strand":1,"alleles":["T","A"],"end":140612554,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612554},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612558,"source":"dbSNP","strand":1,"feature_type":"variation","end":140612558,"alleles":["A","G"],"id":"rs1306106432","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","A"],"end":140612563,"feature_type":"variation","strand":1,"source":"dbSNP","start":140612563,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs907529277"},{"clinical_significance":[],"seq_region_name":"7","id":"rs373793416","feature_type":"variation","strand":1,"end":140612564,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612564},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799939760","alleles":["AA","AAA"],"end":140612566,"feature_type":"variation","strand":1,"source":"dbSNP","start":140612565,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs527818427","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612570,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140612570},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130706123","end":140612571,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140612571,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["G","T"],"end":140612572,"strand":1,"feature_type":"variation","start":140612572,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs772784795","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612573,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140612573,"clinical_significance":[],"seq_region_name":"7","id":"rs1799940005"},{"clinical_significance":[],"seq_region_name":"7","id":"rs552619688","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612580,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140612580},{"seq_region_name":"7","id":"rs1585755506","clinical_significance":[],"alleles":["A","C"],"end":140612582,"strand":1,"feature_type":"variation","start":140612582,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs987827176","clinical_significance":[],"start":140612583,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140612583,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"alleles":["C","T"],"end":140612584,"feature_type":"variation","strand":1,"source":"dbSNP","start":140612584,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1409915005"},{"seq_region_name":"7","id":"rs762677498","clinical_significance":[],"strand":1,"feature_type":"variation","end":140612587,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612587,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140612588,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612588,"source":"dbSNP","seq_region_name":"7","id":"rs1585755536","clinical_significance":[]},{"source":"dbSNP","start":140612589,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140612589,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799940629"},{"strand":1,"feature_type":"variation","end":140612590,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612590,"source":"dbSNP","seq_region_name":"7","id":"rs1799940709","clinical_significance":[]},{"start":140612591,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140612591,"strand":1,"feature_type":"variation","id":"rs1040253720","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1389402447","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140612592,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612592,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs751485454","source":"dbSNP","start":140612593,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140612593,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140612594,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140612594,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1370804207"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612595,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C","T"],"end":140612595,"seq_region_name":"7","id":"rs564372666","clinical_significance":[]},{"end":140612604,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140612604,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs949317684","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1306791182","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140612605,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612605},{"seq_region_name":"7","id":"rs1799941761","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612611,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140612611},{"clinical_significance":[],"seq_region_name":"7","id":"rs185213725","end":140612615,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140612615,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["G","A"],"end":140612620,"feature_type":"variation","strand":1,"source":"dbSNP","start":140612620,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1453400253"},{"seq_region_name":"7","id":"rs1248149689","clinical_significance":[],"end":140612629,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140612629,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140612637,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140612637,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799942102"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799942183","source":"dbSNP","start":140612637,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140612638,"alleles":["AA","A"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612638,"feature_type":"variation","strand":1,"end":140612638,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799942289"},{"seq_region_name":"7","id":"rs980706150","clinical_significance":[],"end":140612639,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140612639,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140612642,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140612642,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799942452","clinical_significance":[]},{"end":140612643,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140612643,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799942532"},{"id":"rs1799942618","seq_region_name":"7","clinical_significance":[],"start":140612644,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140612644,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1799942732","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612646,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140612646},{"feature_type":"variation","strand":1,"alleles":["CC","C"],"end":140612653,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612652,"clinical_significance":[],"id":"rs2130706243","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1384036377","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140612658,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612658},{"seq_region_name":"7","id":"rs553126777","clinical_significance":[],"start":140612659,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140612659,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140612660,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612660,"clinical_significance":[],"id":"rs1799943005","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130706268","feature_type":"variation","strand":1,"end":140612662,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612662},{"feature_type":"variation","strand":1,"end":140612663,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612663,"clinical_significance":[],"seq_region_name":"7","id":"rs1260012990"},{"alleles":["G","C"],"end":140612664,"strand":1,"feature_type":"variation","start":140612664,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799943179","clinical_significance":[]},{"seq_region_name":"7","id":"rs941854894","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612665,"source":"dbSNP","strand":1,"feature_type":"variation","end":140612665,"alleles":["C","T"]},{"source":"dbSNP","start":140612668,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C","G"],"end":140612668,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1043951018","seq_region_name":"7"},{"start":140612669,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140612669,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs903721514","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612678,"source":"dbSNP","strand":1,"feature_type":"variation","end":140612678,"alleles":["T","A"],"seq_region_name":"7","id":"rs1233899878","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140612683,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612683,"source":"dbSNP","seq_region_name":"7","id":"rs1799943604","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799943685","clinical_significance":[],"strand":1,"feature_type":"variation","end":140612690,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612690,"source":"dbSNP"},{"seq_region_name":"7","id":"rs751144896","clinical_significance":[],"strand":1,"feature_type":"variation","end":140612694,"alleles":["A","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612694,"source":"dbSNP"},{"end":140612697,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140612697,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799943870","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs115572449","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140612698,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612698},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140612700,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612700,"source":"dbSNP","id":"rs1206044911","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130706331","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140612703,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612703},{"clinical_significance":[],"id":"rs1052556318","seq_region_name":"7","source":"dbSNP","start":140612704,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140612704,"alleles":["A","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799944257","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612709,"feature_type":"variation","strand":1,"end":140612709,"alleles":["C","T"]},{"start":140612710,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140612710,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1563178295","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs930088872","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140612712,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612712},{"seq_region_name":"7","id":"rs568725964","clinical_significance":[],"alleles":["C","T"],"end":140612721,"strand":1,"feature_type":"variation","start":140612721,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["G","GG"],"end":140612722,"strand":1,"feature_type":"variation","start":140612722,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1253278347","clinical_significance":[]},{"alleles":["G","A"],"end":140612722,"feature_type":"variation","strand":1,"source":"dbSNP","start":140612722,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1357836955"},{"source":"dbSNP","start":140612725,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140612725,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799944777"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799944882","source":"dbSNP","start":140612727,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140612727,"alleles":["C","T"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140612729,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140612729,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs896475479","seq_region_name":"7"},{"alleles":["C","A"],"end":140612733,"strand":1,"feature_type":"variation","start":140612733,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1799945046","seq_region_name":"7","clinical_significance":[]},{"id":"rs1047052399","seq_region_name":"7","clinical_significance":[],"start":140612742,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140612742,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs189872840","clinical_significance":[],"strand":1,"feature_type":"variation","end":140612744,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612744,"source":"dbSNP"},{"start":140612745,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140612745,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1008464220","clinical_significance":[]},{"start":140612749,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140612749,"alleles":["A","T"],"strand":1,"feature_type":"variation","id":"rs1256541650","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612750,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140612750,"seq_region_name":"7","id":"rs1799945523","clinical_significance":[]},{"start":140612759,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140612759,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130706421","clinical_significance":[]},{"seq_region_name":"7","id":"rs146418793","clinical_significance":[],"start":140612762,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140612762,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612765,"feature_type":"variation","strand":1,"end":140612765,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs969631817"},{"seq_region_name":"7","id":"rs899983621","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612767,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140612767},{"alleles":["C","T"],"end":140612768,"strand":1,"feature_type":"variation","start":140612768,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1182324051","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612770,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140612770,"clinical_significance":[],"seq_region_name":"7","id":"rs2130706449"},{"seq_region_name":"7","id":"rs1799945991","clinical_significance":[],"alleles":["T","A"],"end":140612775,"strand":1,"feature_type":"variation","start":140612775,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1181612520","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140612777,"strand":1,"feature_type":"variation","start":140612777,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140612779,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612779,"source":"dbSNP","seq_region_name":"7","id":"rs1484179470","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612780,"source":"dbSNP","strand":1,"feature_type":"variation","end":140612780,"alleles":["G","T"],"seq_region_name":"7","id":"rs1000996983","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799946396","clinical_significance":[],"start":140612781,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140612781,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140612782,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612782,"source":"dbSNP","id":"rs1384537487","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612783,"source":"dbSNP","strand":1,"feature_type":"variation","end":140612783,"alleles":["T","A","G"],"seq_region_name":"7","id":"rs1429813730","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612790,"source":"dbSNP","strand":1,"feature_type":"variation","end":140612790,"alleles":["C","A"],"seq_region_name":"7","id":"rs1032013323","clinical_significance":[]},{"start":140612793,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140612793,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1171969220","clinical_significance":[]},{"alleles":["G","A","C"],"end":140612794,"strand":1,"feature_type":"variation","start":140612794,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs995654491","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612795,"feature_type":"variation","strand":1,"alleles":["T","TT"],"end":140612795,"clinical_significance":[],"seq_region_name":"7","id":"rs1799946969"},{"id":"rs1276957407","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140612800,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612800,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1461140884","clinical_significance":[],"end":140612804,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140612804,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1303090911","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140612808,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612808,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612810,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140612810,"seq_region_name":"7","id":"rs566245922","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612811,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140612811,"clinical_significance":[],"seq_region_name":"7","id":"rs1799947655"},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140612819,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612819,"clinical_significance":[],"id":"rs1585755899","seq_region_name":"7"},{"start":140612823,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140612823,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs1313503160","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140612830,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612830,"source":"dbSNP","seq_region_name":"7","id":"rs951616961","clinical_significance":[]},{"start":140612832,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140612832,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585755926","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799948115","end":140612834,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140612834,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612835,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140612835,"clinical_significance":[],"seq_region_name":"7","id":"rs1377617670"},{"id":"rs983587027","seq_region_name":"7","clinical_significance":[],"start":140612836,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140612836,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs988324830","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140612837,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612837},{"clinical_significance":[],"seq_region_name":"7","id":"rs965653436","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612839,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140612839},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140612840,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612840,"source":"dbSNP","id":"rs1170049619","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799948713","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612841,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140612841},{"alleles":["C","T"],"end":140612842,"feature_type":"variation","strand":1,"source":"dbSNP","start":140612842,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130706554"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612848,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140612848,"seq_region_name":"7","id":"rs975736255","clinical_significance":[]},{"start":140612853,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140612853,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130706562","clinical_significance":[]},{"seq_region_name":"7","id":"rs1372046138","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612854,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140612854},{"clinical_significance":[],"id":"rs1313553101","seq_region_name":"7","alleles":["T","C"],"end":140612858,"feature_type":"variation","strand":1,"source":"dbSNP","start":140612858,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140612862,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612862,"source":"dbSNP","id":"rs1799949201","seq_region_name":"7","clinical_significance":[]},{"id":"rs1164862527","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612864,"source":"dbSNP","strand":1,"feature_type":"variation","end":140612864,"alleles":["C","G"]},{"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140612867,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612867,"clinical_significance":[],"seq_region_name":"7","id":"rs1425550880"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612869,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140612869,"clinical_significance":[],"seq_region_name":"7","id":"rs1382773259"},{"source":"dbSNP","start":140612879,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140612879,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130706591"},{"alleles":["C","T"],"end":140612885,"strand":1,"feature_type":"variation","start":140612885,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1024625044","clinical_significance":[]},{"clinical_significance":[],"id":"rs970817525","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612886,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140612886},{"start":140612889,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140612889,"alleles":["T","C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1186968177","clinical_significance":[]},{"end":140612893,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140612893,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1799950341","seq_region_name":"7","clinical_significance":[]},{"start":140612894,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140612894,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799950478","clinical_significance":[]},{"source":"dbSNP","start":140612897,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140612897,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1483238505"},{"alleles":["T","C"],"end":140612898,"strand":1,"feature_type":"variation","start":140612898,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799950764","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140612900,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612900,"clinical_significance":[],"seq_region_name":"7","id":"rs533675561"},{"id":"rs1012669610","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140612903,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612903,"source":"dbSNP"},{"alleles":["C","G","T"],"end":140612904,"feature_type":"variation","strand":1,"source":"dbSNP","start":140612904,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1254275923"},{"seq_region_name":"7","id":"rs2130706647","clinical_significance":[],"start":140612905,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140612905,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140612910,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612910,"source":"dbSNP","seq_region_name":"7","id":"rs1585756088","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130706654","clinical_significance":[],"end":140612913,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140612913,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612917,"feature_type":"variation","strand":1,"end":140612917,"alleles":["C","A","G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1215214796"},{"end":140612920,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140612920,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799951700","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140612921,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612921,"clinical_significance":[],"seq_region_name":"7","id":"rs1297867692"},{"seq_region_name":"7","id":"rs1799952030","clinical_significance":[],"strand":1,"feature_type":"variation","end":140612922,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612922,"source":"dbSNP"},{"start":140612926,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140612926,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1305869365","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140612927,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612927,"source":"dbSNP","seq_region_name":"7","id":"rs980653792","clinical_significance":[]},{"alleles":["A","G"],"end":140612928,"feature_type":"variation","strand":1,"source":"dbSNP","start":140612928,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799952514"},{"id":"rs1247068172","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140612930,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612930,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612932,"feature_type":"variation","strand":1,"end":140612932,"alleles":["T","A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs558614816"},{"id":"rs1264000722","seq_region_name":"7","clinical_significance":[],"alleles":["C","A","T"],"end":140612940,"strand":1,"feature_type":"variation","start":140612940,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs926533509","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612941,"feature_type":"variation","strand":1,"end":140612941,"alleles":["G","A","C","T"]},{"seq_region_name":"7","id":"rs182495829","clinical_significance":[],"start":140612942,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140612942,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1389356987","clinical_significance":[],"start":140612943,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140612943,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799953596","end":140612958,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140612958,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799953775","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612968,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140612968},{"clinical_significance":[],"seq_region_name":"7","id":"rs1242431629","source":"dbSNP","start":140612973,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140612973,"alleles":["G","A"],"feature_type":"variation","strand":1},{"start":140612975,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140612975,"strand":1,"feature_type":"variation","id":"rs973228252","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612978,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140612978,"clinical_significance":[],"seq_region_name":"7","id":"rs1799954223"},{"end":140612979,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140612979,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799954375","clinical_significance":[]},{"seq_region_name":"7","id":"rs919116033","clinical_significance":[],"strand":1,"feature_type":"variation","end":140612980,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612980,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799954598","clinical_significance":[],"start":140612981,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140612981,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1188245377","alleles":["G","A"],"end":140612983,"feature_type":"variation","strand":1,"source":"dbSNP","start":140612983,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140612988,"source":"dbSNP","strand":1,"feature_type":"variation","end":140612988,"alleles":["C","G"],"seq_region_name":"7","id":"rs1293623239","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs930066381","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140612989,"feature_type":"variation","strand":1,"end":140612989,"alleles":["C","G"]},{"seq_region_name":"7","id":"rs1799954997","clinical_significance":[],"end":140613001,"alleles":["C","-"],"strand":1,"feature_type":"variation","start":140613001,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140613004,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140613004,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1415623874"},{"start":140613010,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140613010,"strand":1,"feature_type":"variation","id":"rs1585756240","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1047615863","source":"dbSNP","start":140613012,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140613012,"alleles":["G","C"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["T","-"],"end":140613014,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613014,"clinical_significance":[],"id":"rs1416713817","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799955486","source":"dbSNP","start":140613015,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140613015,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1413958829","alleles":["G","C"],"end":140613017,"feature_type":"variation","strand":1,"source":"dbSNP","start":140613017,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140613022,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140613022,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1179389628"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140613027,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613027,"clinical_significance":[],"seq_region_name":"7","id":"rs751898746"},{"id":"rs2130706819","seq_region_name":"7","clinical_significance":[],"alleles":["G","C"],"end":140613028,"strand":1,"feature_type":"variation","start":140613028,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs2130706827","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613029,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140613029},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613031,"feature_type":"variation","strand":1,"end":140613031,"alleles":["T","A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1176251810"},{"feature_type":"variation","strand":1,"end":140613035,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613035,"clinical_significance":[],"seq_region_name":"7","id":"rs1585756305"},{"id":"rs1799956031","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613036,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140613036},{"clinical_significance":[],"id":"rs1268244839","seq_region_name":"7","source":"dbSNP","start":140613037,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140613037,"alleles":["C","T"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140613038,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140613038,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1773161069","seq_region_name":"7"},{"seq_region_name":"7","id":"rs576469502","clinical_significance":[],"end":140613039,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140613039,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1467159869","source":"dbSNP","start":140613045,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140613045,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1273130398","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140613046,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613046},{"source":"dbSNP","start":140613048,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140613048,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1229596524"},{"id":"rs1471154339","seq_region_name":"7","clinical_significance":[],"start":140613049,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140613049,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"start":140613050,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140613050,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1052919971","clinical_significance":[]},{"clinical_significance":[],"id":"rs1585756376","seq_region_name":"7","alleles":["T","G"],"end":140613051,"feature_type":"variation","strand":1,"source":"dbSNP","start":140613051,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["T","C","G"],"end":140613057,"strand":1,"feature_type":"variation","start":140613057,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1405952607","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799957508","clinical_significance":[],"start":140613059,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140613059,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140613060,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613060,"clinical_significance":[],"seq_region_name":"7","id":"rs896591543"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613062,"source":"dbSNP","strand":1,"feature_type":"variation","end":140613062,"alleles":["C","A"],"id":"rs1799957781","seq_region_name":"7","clinical_significance":[]},{"start":140613064,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140613064,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1291167368","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130706919","clinical_significance":[],"strand":1,"feature_type":"variation","end":140613071,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613071,"source":"dbSNP"},{"alleles":["A","C","G","T"],"end":140613074,"feature_type":"variation","strand":1,"source":"dbSNP","start":140613074,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1359879615","seq_region_name":"7"},{"source":"dbSNP","start":140613075,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140613075,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799958291"},{"seq_region_name":"7","id":"rs1799958424","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140613082,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613082,"source":"dbSNP"},{"alleles":["C","G","T"],"end":140613092,"strand":1,"feature_type":"variation","start":140613092,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585756416","clinical_significance":[]},{"id":"rs1799958755","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613094,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140613094},{"seq_region_name":"7","id":"rs1799958892","clinical_significance":[],"start":140613095,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140613095,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613096,"source":"dbSNP","strand":1,"feature_type":"variation","end":140613097,"alleles":["AA","A"],"seq_region_name":"7","id":"rs1799959030","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140613101,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613101,"source":"dbSNP","seq_region_name":"7","id":"rs1388034642","clinical_significance":[]},{"source":"dbSNP","start":140613102,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140613102,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1214064244"},{"start":140613111,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140613111,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799959382","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140613114,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613114,"source":"dbSNP","seq_region_name":"7","id":"rs1284156625","clinical_significance":[]},{"clinical_significance":[],"id":"rs1325986429","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140613116,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613116},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613117,"feature_type":"variation","strand":1,"end":140613117,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1390728117"},{"seq_region_name":"7","id":"rs1232971372","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613118,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AAAAAAAAAAA","AAAAAAAAAA","AAAAAAAAAAAA"],"end":140613128},{"seq_region_name":"7","id":"rs1799959849","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613119,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140613119},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613120,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140613120,"id":"rs1378458687","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613123,"source":"dbSNP","strand":1,"feature_type":"variation","end":140613123,"alleles":["A","G"],"seq_region_name":"7","id":"rs2130706999","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799960048","feature_type":"variation","strand":1,"end":140613129,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613129},{"strand":1,"feature_type":"variation","end":140613131,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613131,"source":"dbSNP","seq_region_name":"7","id":"rs1221436637","clinical_significance":[]},{"id":"rs1799960252","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140613134,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613134,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799960346","source":"dbSNP","start":140613136,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140613136,"alleles":["C","T"],"feature_type":"variation","strand":1},{"start":140613137,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140613137,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585756489","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1201210648","source":"dbSNP","start":140613144,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140613144,"alleles":["A","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1013553971","seq_region_name":"7","source":"dbSNP","start":140613146,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C","G"],"end":140613146,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585756512","feature_type":"variation","strand":1,"end":140613149,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613149},{"start":140613151,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140613151,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1262239273","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1209432137","source":"dbSNP","start":140613154,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140613154,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1466651774","clinical_significance":[],"start":140613155,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140613155,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs537407900","source":"dbSNP","start":140613156,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140613156,"alleles":["G","A","C","T"],"feature_type":"variation","strand":1},{"start":140613159,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140613159,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1217787875","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140613161,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613161,"clinical_significance":[],"id":"rs1799961525","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140613163,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613163,"clinical_significance":[],"seq_region_name":"7","id":"rs1799961616"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1045097860","alleles":["G","A"],"end":140613167,"feature_type":"variation","strand":1,"source":"dbSNP","start":140613167,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799961787","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613171,"feature_type":"variation","strand":1,"end":140613171,"alleles":["C","G"]},{"start":140613179,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140613179,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs535705668","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613186,"source":"dbSNP","strand":1,"feature_type":"variation","end":140613186,"alleles":["C","T"],"id":"rs1799961962","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799962054","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613187,"feature_type":"variation","strand":1,"end":140613187,"alleles":["A","AA"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563178577","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613188,"feature_type":"variation","strand":1,"end":140613188,"alleles":["G","A"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613189,"feature_type":"variation","strand":1,"end":140613189,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1236093256"},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140613190,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613190,"source":"dbSNP","seq_region_name":"7","id":"rs187332392","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1485257514","source":"dbSNP","start":140613194,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140613194,"feature_type":"variation","strand":1},{"end":140613195,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140613195,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1039899879"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140613205,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613205,"clinical_significance":[],"seq_region_name":"7","id":"rs1799962583"},{"clinical_significance":[],"id":"rs1435117859","seq_region_name":"7","alleles":["G","C"],"end":140613208,"feature_type":"variation","strand":1,"source":"dbSNP","start":140613208,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140613209,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140613209,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1191330205"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799963634","end":140613211,"alleles":["-","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140613212,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140613212,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140613212,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799963720","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799963821","clinical_significance":[],"strand":1,"feature_type":"variation","end":140613216,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613216,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799963908","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613224,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140613224},{"alleles":["G","A"],"end":140613225,"strand":1,"feature_type":"variation","start":140613225,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1799964018","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs900096689","end":140613227,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140613227,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140613233,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613233,"source":"dbSNP","seq_region_name":"7","id":"rs1430944732","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140613235,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613235,"source":"dbSNP","seq_region_name":"7","id":"rs1001112911","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs996158788","feature_type":"variation","strand":1,"end":140613236,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613236},{"seq_region_name":"7","id":"rs557393992","clinical_significance":[],"strand":1,"feature_type":"variation","end":140613237,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613237,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1585756685","seq_region_name":"7","source":"dbSNP","start":140613238,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140613238,"alleles":["A","C","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1174074591","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613239,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140613239},{"end":140613251,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140613251,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799965131","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613252,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140613252,"clinical_significance":[],"seq_region_name":"7","id":"rs1799965279"},{"end":140613254,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140613254,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799965420"},{"seq_region_name":"7","id":"rs1433163298","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140613259,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613259,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1585756713","seq_region_name":"7","alleles":["C","A","T"],"end":140613260,"feature_type":"variation","strand":1,"source":"dbSNP","start":140613260,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613265,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140613265,"clinical_significance":[],"seq_region_name":"7","id":"rs1585756724"},{"clinical_significance":[],"id":"rs892651794","seq_region_name":"7","end":140613267,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140613267,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613270,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140613270,"id":"rs574361743","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","C"],"end":140613276,"strand":1,"feature_type":"variation","start":140613276,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1189304837","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1428968600","clinical_significance":[],"alleles":["C","T"],"end":140613277,"strand":1,"feature_type":"variation","start":140613277,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140613278,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140613278,"strand":1,"feature_type":"variation","id":"rs2130707223","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","G"],"end":140613284,"feature_type":"variation","strand":1,"source":"dbSNP","start":140613284,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1240891814","seq_region_name":"7"},{"seq_region_name":"7","id":"rs951616439","clinical_significance":[],"start":140613288,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140613288,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1585756778","clinical_significance":[],"strand":1,"feature_type":"variation","end":140613289,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613289,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140613300,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613300,"source":"dbSNP","seq_region_name":"7","id":"rs1799967090","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613303,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140613303,"seq_region_name":"7","id":"rs1799967232","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799967386","clinical_significance":[],"end":140613304,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140613304,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140613311,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613311,"source":"dbSNP","seq_region_name":"7","id":"rs1799967517","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1443468506","end":140613313,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140613313,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613314,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140613314,"clinical_significance":[],"seq_region_name":"7","id":"rs1401659999"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613316,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140613316,"seq_region_name":"7","id":"rs1799967802","clinical_significance":[]},{"start":140613321,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140613321,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1209161539","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140613327,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613327,"clinical_significance":[],"id":"rs1344013782","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613334,"source":"dbSNP","strand":1,"feature_type":"variation","end":140613334,"alleles":["G","A"],"seq_region_name":"7","id":"rs1430085834","clinical_significance":[]},{"source":"dbSNP","start":140613335,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140613335,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1279082614"},{"seq_region_name":"7","id":"rs1303880190","clinical_significance":[],"start":140613336,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140613336,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"id":"rs1799968329","seq_region_name":"7","clinical_significance":[],"alleles":["AGA","A"],"end":140613341,"strand":1,"feature_type":"variation","start":140613339,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140613342,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613342,"source":"dbSNP","seq_region_name":"7","id":"rs1004396373","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140613348,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613348,"clinical_significance":[],"seq_region_name":"7","id":"rs1014602337"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799968650","alleles":["T","C"],"end":140613352,"feature_type":"variation","strand":1,"source":"dbSNP","start":140613352,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1403288518","clinical_significance":[],"strand":1,"feature_type":"variation","end":140613355,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613355,"source":"dbSNP"},{"start":140613357,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140613357,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799968863","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140613360,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613360,"clinical_significance":[],"seq_region_name":"7","id":"rs1282903322"},{"clinical_significance":[],"id":"rs1340984460","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["AAA","AA"],"end":140613364,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613362},{"alleles":["A","T"],"end":140613369,"strand":1,"feature_type":"variation","start":140613369,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1009294120","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs865849804","end":140613370,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140613370,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","T"],"end":140613371,"feature_type":"variation","strand":1,"source":"dbSNP","start":140613371,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1424197714"},{"seq_region_name":"7","id":"rs1799969408","clinical_significance":[],"start":140613373,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140613373,"strand":1,"feature_type":"variation"},{"id":"rs1799969555","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140613376,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613376,"source":"dbSNP"},{"source":"dbSNP","start":140613377,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140613377,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799969717"},{"alleles":["A","T"],"end":140613382,"feature_type":"variation","strand":1,"source":"dbSNP","start":140613382,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs542092724"},{"source":"dbSNP","start":140613383,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140613383,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799969920"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585756916","end":140613385,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140613385,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140613386,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613386,"source":"dbSNP","seq_region_name":"7","id":"rs1799970104","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1351043405","source":"dbSNP","start":140613386,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140613390,"alleles":["AAAAA","AAAA"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1025157339","source":"dbSNP","start":140613390,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C","G"],"end":140613390,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613396,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140613396,"clinical_significance":[],"seq_region_name":"7","id":"rs113238509"},{"alleles":["G","A","C"],"end":140613397,"feature_type":"variation","strand":1,"source":"dbSNP","start":140613397,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs542552622"},{"end":140613400,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140613400,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1222542059"},{"feature_type":"variation","strand":1,"end":140613401,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613401,"clinical_significance":[],"seq_region_name":"7","id":"rs1186258956"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613401,"source":"dbSNP","strand":1,"feature_type":"variation","end":140613409,"alleles":["GTGGTGGTG","GTGGTG"],"id":"rs1239665143","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1485526776","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613404,"source":"dbSNP","strand":1,"feature_type":"variation","end":140613404,"alleles":["G","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130707419","source":"dbSNP","start":140613406,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140613406,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140613407,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613407,"source":"dbSNP","seq_region_name":"7","id":"rs1799971089","clinical_significance":[]},{"source":"dbSNP","start":140613409,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140613409,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1256394784"},{"start":140613410,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140613410,"strand":1,"feature_type":"variation","id":"rs1205484359","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1308857752","source":"dbSNP","start":140613412,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140613412,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799971504","alleles":["A","G"],"end":140613419,"feature_type":"variation","strand":1,"source":"dbSNP","start":140613419,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585757052","alleles":["G","A"],"end":140613420,"feature_type":"variation","strand":1,"source":"dbSNP","start":140613420,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1270350565","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613421,"source":"dbSNP","strand":1,"feature_type":"variation","end":140613421,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1799971770","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613423,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140613423},{"clinical_significance":[],"seq_region_name":"7","id":"rs1001871049","source":"dbSNP","start":140613424,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140613424,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs975684014","seq_region_name":"7","feature_type":"variation","strand":1,"end":140613426,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613426},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613430,"source":"dbSNP","strand":1,"feature_type":"variation","end":140613430,"alleles":["C","G"],"seq_region_name":"7","id":"rs921601168","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1480608663","feature_type":"variation","strand":1,"end":140613431,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613431},{"seq_region_name":"7","id":"rs764129561","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613431,"source":"dbSNP","strand":1,"feature_type":"variation","end":140613432,"alleles":["TT","T"]},{"id":"rs1489650680","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140613435,"strand":1,"feature_type":"variation","start":140613435,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613441,"source":"dbSNP","strand":1,"feature_type":"variation","end":140613441,"alleles":["G","A"],"seq_region_name":"7","id":"rs953099398","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140613442,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613442,"clinical_significance":[],"seq_region_name":"7","id":"rs1033382338"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613447,"source":"dbSNP","strand":1,"feature_type":"variation","end":140613447,"alleles":["G","A"],"id":"rs1799972616","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140613448,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140613448,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs963280985"},{"seq_region_name":"7","id":"rs1470712889","clinical_significance":[],"alleles":["C","G"],"end":140613454,"strand":1,"feature_type":"variation","start":140613454,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613455,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140613455,"seq_region_name":"7","id":"rs1160709331","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799973033","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140613456,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613456},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140613461,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613461,"source":"dbSNP","seq_region_name":"7","id":"rs1585757149","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799973240","source":"dbSNP","start":140613472,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","-"],"end":140613472,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs973349225","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140613476,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613476},{"seq_region_name":"7","id":"rs1563178724","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140613477,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613477,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799973528","alleles":["C","T"],"end":140613480,"feature_type":"variation","strand":1,"source":"dbSNP","start":140613480,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799973612","source":"dbSNP","start":140613481,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140613481,"alleles":["A","G"],"feature_type":"variation","strand":1},{"id":"rs144605212","seq_region_name":"7","clinical_significance":[],"start":140613483,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140613483,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs561276093","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613484,"source":"dbSNP","strand":1,"feature_type":"variation","end":140613484,"alleles":["G","A"]},{"clinical_significance":[],"id":"rs982859833","seq_region_name":"7","alleles":["C","T"],"end":140613488,"feature_type":"variation","strand":1,"source":"dbSNP","start":140613488,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs912647129","end":140613489,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140613489,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140613496,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613496,"source":"dbSNP","seq_region_name":"7","id":"rs1799974093","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs996109585","source":"dbSNP","start":140613497,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C","G"],"end":140613497,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs917974309","source":"dbSNP","start":140613498,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140613498,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1799974440","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140613500,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613500,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613501,"source":"dbSNP","strand":1,"feature_type":"variation","end":140613501,"alleles":["T","C"],"seq_region_name":"7","id":"rs1799974524","clinical_significance":[]},{"start":140613505,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140613505,"alleles":["A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585757216","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs949439336","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140613508,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613508},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799974817","source":"dbSNP","start":140613509,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140613509,"feature_type":"variation","strand":1},{"start":140613511,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140613511,"alleles":["G","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1184773413","clinical_significance":[]},{"seq_region_name":"7","id":"rs531743916","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613514,"source":"dbSNP","strand":1,"feature_type":"variation","end":140613514,"alleles":["T","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799975066","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613515,"feature_type":"variation","strand":1,"end":140613515,"alleles":["G","A"]},{"feature_type":"variation","strand":1,"end":140613519,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613519,"clinical_significance":[],"seq_region_name":"7","id":"rs1799975164"},{"source":"dbSNP","start":140613521,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140613521,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs550173078"},{"feature_type":"variation","strand":1,"alleles":["A","-"],"end":140613524,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613524,"clinical_significance":[],"seq_region_name":"7","id":"rs1230758503"},{"source":"dbSNP","start":140613524,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140613524,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799975346"},{"end":140613526,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140613526,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1302775745","clinical_significance":[]},{"id":"rs1799975748","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140613527,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613527,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140613531,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613531,"clinical_significance":[],"seq_region_name":"7","id":"rs1799975840"},{"strand":1,"feature_type":"variation","end":140613532,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613532,"source":"dbSNP","seq_region_name":"7","id":"rs1799976112","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130707638","clinical_significance":[],"start":140613535,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140613535,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"id":"rs1799976241","seq_region_name":"7","clinical_significance":[],"alleles":["T","A"],"end":140613536,"strand":1,"feature_type":"variation","start":140613536,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1336637762","feature_type":"variation","strand":1,"end":140613537,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613537},{"alleles":["T","A"],"end":140613538,"feature_type":"variation","strand":1,"source":"dbSNP","start":140613538,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1274487916","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613539,"feature_type":"variation","strand":1,"end":140613538,"alleles":["-","A","AA"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799976699"},{"source":"dbSNP","start":140613539,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140613539,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1278169453","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799976941","end":140613539,"alleles":["C","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140613539,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140613540,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140613540,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1444085050"},{"clinical_significance":[],"id":"rs769852380","seq_region_name":"7","source":"dbSNP","start":140613540,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140613554,"alleles":["AAAAAAAAAAAAAAA","AAAAAAAAAAA","AAAAAAAAAAAA","AAAAAAAAAAAAA","AAAAAAAAAAAAAA","AAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAA"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1437310007","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613544,"source":"dbSNP","strand":1,"feature_type":"variation","end":140613544,"alleles":["A","G"]},{"clinical_significance":[],"id":"rs1045212090","seq_region_name":"7","feature_type":"variation","strand":1,"end":140613546,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613546},{"id":"rs1799977550","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613554,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G","T"],"end":140613554},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613555,"feature_type":"variation","strand":1,"end":140613555,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585757375"},{"strand":1,"feature_type":"variation","end":140613556,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613556,"source":"dbSNP","id":"rs905175991","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1461435941","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140613560,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613560},{"strand":1,"feature_type":"variation","end":140613561,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613561,"source":"dbSNP","seq_region_name":"7","id":"rs1799977886","clinical_significance":[]},{"id":"rs1389998714","seq_region_name":"7","clinical_significance":[],"start":140613562,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140613562,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1799978058","seq_region_name":"7","end":140613563,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140613563,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140613565,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140613565,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799978151"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799978305","source":"dbSNP","start":140613566,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140613566,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140613572,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613572,"clinical_significance":[],"seq_region_name":"7","id":"rs1328247887"},{"alleles":["G","A"],"end":140613575,"strand":1,"feature_type":"variation","start":140613575,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1799978640","seq_region_name":"7","clinical_significance":[]},{"start":140613579,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140613585,"alleles":["CACAGCA","CACAGCACAGCA"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1161749045","clinical_significance":[]},{"seq_region_name":"7","id":"rs2968563","clinical_significance":[],"strand":1,"feature_type":"variation","end":140613581,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613581,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799979198","feature_type":"variation","strand":1,"end":140613582,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613582},{"clinical_significance":[],"seq_region_name":"7","id":"rs1246557688","end":140613583,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140613583,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140613584,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140613584,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1049090547","clinical_significance":[]},{"end":140613589,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140613589,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130707781","clinical_significance":[]},{"start":140613590,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140613590,"strand":1,"feature_type":"variation","id":"rs1293868669","seq_region_name":"7","clinical_significance":[]},{"end":140613591,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140613591,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1799979796","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613592,"source":"dbSNP","strand":1,"feature_type":"variation","end":140613592,"alleles":["C","T"],"seq_region_name":"7","id":"rs1585757467","clinical_significance":[]},{"source":"dbSNP","start":140613593,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140613593,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1356559163"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1221178602","source":"dbSNP","start":140613612,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140613612,"alleles":["A","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1273250456","clinical_significance":[],"start":140613615,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140613615,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140613617,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140613617,"alleles":["A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799980525"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799980652","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613618,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140613618},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799980756","alleles":["TGCCTATGGGGTAGCCCTGCTTTGCCTATGG","TGCCTATGG"],"end":140613651,"feature_type":"variation","strand":1,"source":"dbSNP","start":140613621,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1211262964","alleles":["T","C"],"end":140613627,"feature_type":"variation","strand":1,"source":"dbSNP","start":140613627,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1439242445","clinical_significance":[],"strand":1,"feature_type":"variation","end":140613630,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613630,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613631,"feature_type":"variation","strand":1,"end":140613631,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1799981137"},{"seq_region_name":"7","id":"rs2130707849","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140613632,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613632,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613633,"source":"dbSNP","strand":1,"feature_type":"variation","end":140613633,"alleles":["A","G"],"id":"rs1799981279","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs754101796","clinical_significance":[],"start":140613635,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140613635,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1799981602","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613635,"source":"dbSNP","strand":1,"feature_type":"variation","end":140613637,"alleles":["CCC","CC"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613636,"source":"dbSNP","strand":1,"feature_type":"variation","end":140613636,"alleles":["C","A","T"],"seq_region_name":"7","id":"rs887382886","clinical_significance":[]},{"alleles":["G","T"],"end":140613639,"strand":1,"feature_type":"variation","start":140613639,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799981930","clinical_significance":[]},{"clinical_significance":[],"id":"rs1585757546","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613646,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140613646},{"alleles":["T","C"],"end":140613647,"strand":1,"feature_type":"variation","start":140613647,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1231487107","seq_region_name":"7","clinical_significance":[]},{"start":140613648,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140613648,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1039676367","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1439487106","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613649,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140613649},{"seq_region_name":"7","id":"rs1799982365","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140613653,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613653,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799982457","clinical_significance":[],"end":140613654,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140613654,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140613657,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140613657,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1004748540"},{"strand":1,"feature_type":"variation","end":140613659,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613659,"source":"dbSNP","seq_region_name":"7","id":"rs1799982675","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140613660,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613660,"clinical_significance":[],"seq_region_name":"7","id":"rs921299400"},{"clinical_significance":[],"id":"rs1387710774","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613661,"feature_type":"variation","strand":1,"end":140613661,"alleles":["C","T"]},{"feature_type":"variation","strand":1,"end":140613662,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613662,"clinical_significance":[],"seq_region_name":"7","id":"rs1442844497"},{"strand":1,"feature_type":"variation","end":140613663,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613663,"source":"dbSNP","seq_region_name":"7","id":"rs1301409668","clinical_significance":[]},{"end":140613664,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140613664,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1440188089","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799983624","clinical_significance":[],"end":140613668,"alleles":["AAAA","AAAAA"],"strand":1,"feature_type":"variation","start":140613665,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140613669,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140613669,"strand":1,"feature_type":"variation","id":"rs1162794618","seq_region_name":"7","clinical_significance":[]},{"end":140613670,"alleles":["TT","T"],"strand":1,"feature_type":"variation","start":140613669,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1366559965","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["TT","-"],"end":140613670,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613669,"clinical_significance":[],"seq_region_name":"7","id":"rs1799984054"},{"end":140613669,"alleles":["-","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140613670,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1799984216"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613670,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140613670,"id":"rs1452237582","seq_region_name":"7","clinical_significance":[]},{"id":"rs74627520","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140613671,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613671,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1019747103","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613671,"feature_type":"variation","strand":1,"end":140613682,"alleles":["AAAAAAAAAAAA","AAAAAAAAAA","AAAAAAAAAAA","AAAAAAAAAAAAA","AAAAAAAAAAAAAA","AAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAA"]},{"id":"rs1799985215","seq_region_name":"7","clinical_significance":[],"start":140613676,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140613676,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140613677,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613677,"source":"dbSNP","seq_region_name":"7","id":"rs936906391","clinical_significance":[]},{"seq_region_name":"7","id":"rs879502034","clinical_significance":[],"start":140613678,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140613678,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs951650647","feature_type":"variation","strand":1,"end":140613679,"alleles":["A","C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613679},{"end":140613680,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140613680,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1411824269","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs869183955","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613680,"feature_type":"variation","strand":1,"alleles":["AAACAAACAAA","AAACAAA"],"end":140613690},{"clinical_significance":[],"seq_region_name":"7","id":"rs767177060","feature_type":"variation","strand":1,"end":140613681,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613681},{"seq_region_name":"7","id":"rs1799985992","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["AACAA","AA"],"end":140613685,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613681,"source":"dbSNP"},{"end":140613681,"alleles":["-","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140613682,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1262368069","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140613682,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613682,"source":"dbSNP","id":"rs529645939","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613682,"feature_type":"variation","strand":1,"alleles":["AC","CA"],"end":140613683,"clinical_significance":[],"seq_region_name":"7","id":"rs796559231"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613682,"feature_type":"variation","strand":1,"end":140613684,"alleles":["ACA","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1491212457"},{"seq_region_name":"7","id":"rs73165441","clinical_significance":[],"end":140613683,"alleles":["C","A","G"],"strand":1,"feature_type":"variation","start":140613683,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs113214152","clinical_significance":[],"alleles":["C","-"],"end":140613683,"strand":1,"feature_type":"variation","start":140613683,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613683,"source":"dbSNP","strand":1,"feature_type":"variation","end":140613683,"alleles":["C","CC"],"seq_region_name":"7","id":"rs199910062","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs796815761","end":140613687,"alleles":["CAAAC","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140613683,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613684,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["-","G"],"end":140613683,"id":"rs1799987243","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140613686,"alleles":["AAA","A","AA","AAAA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613684,"source":"dbSNP","id":"rs1233692664","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1799987495","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613685,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140613685},{"seq_region_name":"7","id":"rs111399339","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613687,"source":"dbSNP","strand":1,"feature_type":"variation","end":140613687,"alleles":["C","A"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613687,"feature_type":"variation","strand":1,"end":140613687,"alleles":["C","-"],"clinical_significance":[],"id":"rs1799987722","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs564457639","end":140613693,"alleles":["AAAAAA","AAAAA","AAAAAAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140613688,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140613689,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140613689,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1361854082"},{"strand":1,"feature_type":"variation","end":140613690,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613690,"source":"dbSNP","seq_region_name":"7","id":"rs979139205","clinical_significance":[]},{"end":140613692,"alleles":["AAA","AAAGAAA"],"strand":1,"feature_type":"variation","start":140613690,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799988136","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613694,"source":"dbSNP","strand":1,"feature_type":"variation","end":140613694,"alleles":["C","A","T"],"seq_region_name":"7","id":"rs1353643698","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140613695,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613695,"source":"dbSNP","seq_region_name":"7","id":"rs1001985549","clinical_significance":[]},{"seq_region_name":"7","id":"rs191535264","clinical_significance":[],"alleles":["C","T"],"end":140613697,"strand":1,"feature_type":"variation","start":140613697,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs114581579","source":"dbSNP","start":140613699,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140613699,"alleles":["G","A"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613702,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140613702,"id":"rs1799988669","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799988760","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613704,"source":"dbSNP","strand":1,"feature_type":"variation","end":140613706,"alleles":["GAT","GATGAT"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1433689154","end":140613705,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140613705,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1373189908","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613707,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140613707},{"end":140613714,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140613714,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs963066238"},{"clinical_significance":[],"id":"rs757569350","seq_region_name":"7","alleles":["A","C"],"end":140613715,"feature_type":"variation","strand":1,"source":"dbSNP","start":140613715,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140613716,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140613725,"alleles":["AAAATAAAAT","AAAAT"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799989246","clinical_significance":[]},{"id":"rs1244569056","seq_region_name":"7","clinical_significance":[],"end":140613718,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140613718,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140613720,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613720,"source":"dbSNP","seq_region_name":"7","id":"rs570163729","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585757961","clinical_significance":[],"end":140613728,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140613728,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1026664908","clinical_significance":[],"strand":1,"feature_type":"variation","end":140613732,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613732,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799989720","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140613734,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613734},{"strand":1,"feature_type":"variation","end":140613738,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613738,"source":"dbSNP","seq_region_name":"7","id":"rs1799989809","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140613740,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613740,"clinical_significance":[],"id":"rs1270234278","seq_region_name":"7"},{"seq_region_name":"7","id":"rs950547435","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140613744,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613744,"source":"dbSNP"},{"end":140613745,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140613745,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1188392510","seq_region_name":"7"},{"alleles":["A","G"],"end":140613751,"strand":1,"feature_type":"variation","start":140613751,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1486505601","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799990255","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613763,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140613763},{"clinical_significance":[],"seq_region_name":"7","id":"rs537468842","source":"dbSNP","start":140613769,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140613769,"alleles":["T","C"],"feature_type":"variation","strand":1},{"start":140613772,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140613772,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs987714537","clinical_significance":[]},{"source":"dbSNP","start":140613774,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140613774,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1193660332"},{"end":140613775,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140613775,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1481081652"},{"source":"dbSNP","start":140613786,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C","G"],"end":140613786,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585758058"},{"seq_region_name":"7","id":"rs1018818995","clinical_significance":[],"strand":1,"feature_type":"variation","end":140613787,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613787,"source":"dbSNP"},{"seq_region_name":"7","id":"rs555775019","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140613788,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613788,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613789,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140613789,"clinical_significance":[],"id":"rs1799991058","seq_region_name":"7"},{"start":140613794,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140613794,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1225260070","clinical_significance":[]},{"clinical_significance":[],"id":"rs1457599767","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613795,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140613795},{"seq_region_name":"7","id":"rs1799991438","clinical_significance":[],"strand":1,"feature_type":"variation","end":140613798,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613798,"source":"dbSNP"},{"id":"rs1799991578","seq_region_name":"7","clinical_significance":[],"start":140613812,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140613812,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1314015408","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613814,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140613814},{"seq_region_name":"7","id":"rs1799991780","clinical_significance":[],"alleles":["G","A"],"end":140613815,"strand":1,"feature_type":"variation","start":140613815,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1235557403","source":"dbSNP","start":140613818,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140613818,"alleles":["A","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1204779287","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613819,"feature_type":"variation","strand":1,"end":140613819,"alleles":["G","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613824,"feature_type":"variation","strand":1,"end":140613824,"alleles":["A","C"],"clinical_significance":[],"id":"rs1354008116","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140613830,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613830,"clinical_significance":[],"seq_region_name":"7","id":"rs1799992161"},{"clinical_significance":[],"id":"rs965426478","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613831,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140613831},{"end":140613837,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140613837,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1563179004","clinical_significance":[]},{"seq_region_name":"7","id":"rs1799992420","clinical_significance":[],"start":140613842,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140613841,"alleles":["-","GCACCAACATG"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613842,"source":"dbSNP","strand":1,"feature_type":"variation","end":140613842,"alleles":["T","C"],"seq_region_name":"7","id":"rs917753318","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613844,"feature_type":"variation","strand":1,"end":140613844,"alleles":["T","G"],"clinical_significance":[],"id":"rs1799992616","seq_region_name":"7"},{"source":"dbSNP","start":140613845,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140613845,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799992716"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799992815","end":140613847,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140613847,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140613850,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140613850,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1799992910"},{"alleles":["A","G"],"end":140613855,"strand":1,"feature_type":"variation","start":140613855,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1245489927","clinical_significance":[]},{"id":"rs567698741","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613858,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140613858},{"clinical_significance":[],"seq_region_name":"7","id":"rs1396748354","end":140613859,"alleles":["A","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140613859,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140613862,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613862,"clinical_significance":[],"seq_region_name":"7","id":"rs565570921"},{"end":140613863,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140613863,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799993444","clinical_significance":[]},{"end":140613865,"alleles":["A","C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140613865,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs535429001"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799993695","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613866,"feature_type":"variation","strand":1,"end":140613875,"alleles":["CTGAGAGCTG","CTG"]},{"alleles":["G","A"],"end":140613870,"strand":1,"feature_type":"variation","start":140613870,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799993799","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1165631004","alleles":["A","-"],"end":140613871,"feature_type":"variation","strand":1,"source":"dbSNP","start":140613871,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613872,"feature_type":"variation","strand":1,"end":140613872,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs778828998"},{"start":140613876,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C"],"end":140613876,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs931280118","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1415489100","alleles":["G","C"],"end":140613879,"feature_type":"variation","strand":1,"source":"dbSNP","start":140613879,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1476438413","end":140613880,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140613880,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1419910393","clinical_significance":[],"start":140613881,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140613881,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613885,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140613885,"clinical_significance":[],"id":"rs1252846401","seq_region_name":"7"},{"id":"rs1194183066","seq_region_name":"7","clinical_significance":[],"alleles":["C","A"],"end":140613898,"strand":1,"feature_type":"variation","start":140613898,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1480323064","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613899,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140613899},{"seq_region_name":"7","id":"rs1799994673","clinical_significance":[],"end":140613900,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140613900,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613906,"source":"dbSNP","strand":1,"feature_type":"variation","end":140613906,"alleles":["C","A"],"seq_region_name":"7","id":"rs921240638","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799994880","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613907,"feature_type":"variation","strand":1,"end":140613907,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799994955","alleles":["T","C"],"end":140613908,"feature_type":"variation","strand":1,"source":"dbSNP","start":140613908,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613912,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140613912,"seq_region_name":"7","id":"rs936687678","clinical_significance":[]},{"clinical_significance":[],"id":"rs1166299241","seq_region_name":"7","source":"dbSNP","start":140613914,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140613914,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1585758292","clinical_significance":[],"start":140613915,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140613915,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs554025337","seq_region_name":"7","end":140613916,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140613916,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140613917,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140613917,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs940267095","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613918,"feature_type":"variation","strand":1,"end":140613918,"alleles":["A","G"],"clinical_significance":[],"id":"rs1041306474","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1799995672","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613919,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140613919},{"alleles":["A","C"],"end":140613923,"feature_type":"variation","strand":1,"source":"dbSNP","start":140613923,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs151157994"},{"seq_region_name":"7","id":"rs2130708456","clinical_significance":[],"start":140613925,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140613925,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs7796944","seq_region_name":"7","source":"dbSNP","start":140613926,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140613926,"feature_type":"variation","strand":1},{"end":140613929,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140613929,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs562299200"},{"seq_region_name":"7","id":"rs1799996150","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140613934,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613934,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1799996265","clinical_significance":[],"start":140613941,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140613941,"strand":1,"feature_type":"variation"},{"end":140613942,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140613942,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799996409","clinical_significance":[]},{"start":140613950,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140613950,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","id":"rs1451767769","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs888874664","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613959,"source":"dbSNP","strand":1,"feature_type":"variation","end":140613959,"alleles":["C","G"]},{"end":140613960,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140613960,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130708511","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130708514","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140613964,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613964},{"strand":1,"feature_type":"variation","end":140613967,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613967,"source":"dbSNP","seq_region_name":"7","id":"rs1000906438","clinical_significance":[]},{"alleles":["A","G","T"],"end":140613968,"feature_type":"variation","strand":1,"source":"dbSNP","start":140613968,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs781067883"},{"start":140613969,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G","T"],"end":140613969,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs558307240","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1799997180","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140613972,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613972},{"source":"dbSNP","start":140613984,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140613984,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs140234840"},{"alleles":["T","C"],"end":140613986,"feature_type":"variation","strand":1,"source":"dbSNP","start":140613986,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1470367439","seq_region_name":"7"},{"end":140613988,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140613988,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1309623203","clinical_significance":[]},{"alleles":["C","A","G","T"],"end":140613989,"strand":1,"feature_type":"variation","start":140613989,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs150348995","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613991,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140613991,"id":"rs898805325","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140613998,"alleles":["CCCC","CCCCC"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613995,"source":"dbSNP","seq_region_name":"7","id":"rs869132128","clinical_significance":[]},{"seq_region_name":"7","id":"rs183796870","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140613997,"source":"dbSNP","strand":1,"feature_type":"variation","end":140613997,"alleles":["C","T"]},{"clinical_significance":[],"id":"rs188683498","seq_region_name":"7","end":140613999,"alleles":["T","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140613999,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1554480966","feature_type":"variation","strand":1,"alleles":["TTTTTT","TTTTT"],"end":140614004,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140613999},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614002,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140614002,"seq_region_name":"7","id":"rs1799998267","clinical_significance":[]},{"seq_region_name":"7","id":"rs1323880789","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140614004,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614004,"source":"dbSNP"},{"source":"dbSNP","start":140614005,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140614005,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs529300161"},{"clinical_significance":[],"seq_region_name":"7","id":"rs886354798","end":140614013,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140614013,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140614017,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140614017,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799998942","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585758540","alleles":["C","T"],"end":140614018,"feature_type":"variation","strand":1,"source":"dbSNP","start":140614018,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","T"],"end":140614019,"strand":1,"feature_type":"variation","start":140614019,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1799999241","clinical_significance":[]},{"seq_region_name":"7","id":"rs1024926439","clinical_significance":[],"start":140614020,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140614020,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563179145","alleles":["C","A"],"end":140614022,"feature_type":"variation","strand":1,"source":"dbSNP","start":140614022,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140614023,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140614023,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1799999531","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs768228276","end":140614026,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140614026,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["CTCACT","CT"],"end":140614031,"feature_type":"variation","strand":1,"source":"dbSNP","start":140614026,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1265344882","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1799999849","seq_region_name":"7","source":"dbSNP","start":140614030,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140614030,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs541399284","end":140614032,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140614032,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140614036,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140614036,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1800000030","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614037,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140614037,"seq_region_name":"7","id":"rs762506776","clinical_significance":[]},{"start":140614041,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140614041,"strand":1,"feature_type":"variation","id":"rs1800000206","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140614042,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614042,"clinical_significance":[],"seq_region_name":"7","id":"rs1800000298"},{"id":"rs1800000395","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140614046,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614046,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs970520117","alleles":["T","C"],"end":140614049,"feature_type":"variation","strand":1,"source":"dbSNP","start":140614049,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1800000602","seq_region_name":"7","clinical_significance":[],"start":140614050,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140614050,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140614052,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G","T"],"end":140614052,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1008850442"},{"seq_region_name":"7","id":"rs1263047828","clinical_significance":[],"strand":1,"feature_type":"variation","end":140614059,"alleles":["A","C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614059,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1259302860","clinical_significance":[],"strand":1,"feature_type":"variation","end":140614062,"alleles":["G","C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614062,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140614063,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614063,"source":"dbSNP","seq_region_name":"7","id":"rs1800001076","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140614066,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614066,"source":"dbSNP","seq_region_name":"7","id":"rs1800001157","clinical_significance":[]},{"seq_region_name":"7","id":"rs1448803967","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614067,"source":"dbSNP","strand":1,"feature_type":"variation","end":140614069,"alleles":["TTT","TT"]},{"end":140614077,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140614077,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1375682095","clinical_significance":[]},{"seq_region_name":"7","id":"rs1800001492","clinical_significance":[],"end":140614082,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140614082,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1800001588","clinical_significance":[],"alleles":["G","A"],"end":140614083,"strand":1,"feature_type":"variation","start":140614083,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1800001687","seq_region_name":"7","alleles":["G","A"],"end":140614085,"feature_type":"variation","strand":1,"source":"dbSNP","start":140614085,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1191195064","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140614087,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614087,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1262715785","source":"dbSNP","start":140614091,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140614091,"alleles":["G","T"],"feature_type":"variation","strand":1},{"alleles":["T","A","C","G"],"end":140614093,"strand":1,"feature_type":"variation","start":140614093,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1563179164","clinical_significance":[]},{"clinical_significance":[],"id":"rs1800002105","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614095,"feature_type":"variation","strand":1,"end":140614100,"alleles":["TTTTTT","TTTTTTT"]},{"start":140614095,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TTTTTTATTTTTTTATTTTTTATTTTTTT","TTTTTTATTTTTTT"],"end":140614123,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs980616161","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614097,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TTTTATTTT","TTTT"],"end":140614105,"id":"rs1800002319","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563179178","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614099,"feature_type":"variation","strand":1,"end":140614099,"alleles":["T","A"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614100,"source":"dbSNP","strand":1,"feature_type":"variation","end":140614100,"alleles":["T","A"],"seq_region_name":"7","id":"rs1368741633","clinical_significance":[]},{"clinical_significance":[],"id":"rs1325086114","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614102,"feature_type":"variation","strand":1,"alleles":["TTTTTTT","TTTTTTTT"],"end":140614108},{"seq_region_name":"7","id":"rs1386914948","clinical_significance":[],"strand":1,"feature_type":"variation","end":140614122,"alleles":["TTTTTTATTTTTTATTTTTT","TTTTTTATTTTTT","TTTTTTATTTTTTATTTTTTATTTTTT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614103,"source":"dbSNP"},{"start":140614106,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TTTATTT","TTT"],"end":140614112,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1800002823","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140614109,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614109,"clinical_significance":[],"seq_region_name":"7","id":"rs1800002926"},{"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140614110,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614110,"clinical_significance":[],"seq_region_name":"7","id":"rs1453389707"},{"clinical_significance":[],"seq_region_name":"7","id":"rs926658325","source":"dbSNP","start":140614110,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TTTTTT","TTTT"],"end":140614115,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1800003231","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614116,"source":"dbSNP","strand":1,"feature_type":"variation","end":140614116,"alleles":["A","T"]},{"clinical_significance":[],"id":"rs1800003338","seq_region_name":"7","alleles":["TTTTTTT","TTTTTTTT"],"end":140614123,"feature_type":"variation","strand":1,"source":"dbSNP","start":140614117,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140614124,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614124,"clinical_significance":[],"seq_region_name":"7","id":"rs1178881590"},{"start":140614132,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140614132,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs193225055","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614133,"source":"dbSNP","strand":1,"feature_type":"variation","end":140614133,"alleles":["T","A"],"id":"rs984644384","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs2130708816","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614135,"feature_type":"variation","strand":1,"end":140614135,"alleles":["A","G"]},{"source":"dbSNP","start":140614136,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140614136,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1465364004"},{"clinical_significance":[],"id":"rs908523241","seq_region_name":"7","feature_type":"variation","strand":1,"end":140614140,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614140},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140614142,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614142,"clinical_significance":[],"seq_region_name":"7","id":"rs940054775"},{"clinical_significance":[],"id":"rs964532398","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614144,"feature_type":"variation","strand":1,"end":140614144,"alleles":["C","T"]},{"end":140614147,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140614147,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1260159676","seq_region_name":"7"},{"start":140614153,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140614153,"alleles":["G","C"],"strand":1,"feature_type":"variation","id":"rs1041255517","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140614166,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614166,"clinical_significance":[],"seq_region_name":"7","id":"rs1387127625"},{"start":140614167,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140614167,"alleles":["A","C","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs7792863","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585758877","clinical_significance":[],"start":140614168,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140614168,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140614177,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614177,"source":"dbSNP","seq_region_name":"7","id":"rs1800004779","clinical_significance":[]},{"clinical_significance":[],"id":"rs1800004881","seq_region_name":"7","alleles":["C","A","T"],"end":140614182,"feature_type":"variation","strand":1,"source":"dbSNP","start":140614182,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","T"],"end":140614192,"feature_type":"variation","strand":1,"source":"dbSNP","start":140614192,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs185614757"},{"seq_region_name":"7","id":"rs1800005245","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614194,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140614194},{"seq_region_name":"7","id":"rs932783122","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614196,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140614196},{"alleles":["G","A"],"end":140614198,"strand":1,"feature_type":"variation","start":140614198,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1345633326","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1328113942","feature_type":"variation","strand":1,"end":140614200,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614200},{"source":"dbSNP","start":140614206,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140614206,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1800005861","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140614214,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614214,"source":"dbSNP","seq_region_name":"7","id":"rs1800006008","clinical_significance":[]},{"clinical_significance":[],"id":"rs1800006089","seq_region_name":"7","source":"dbSNP","start":140614220,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140614220,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140614222,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614222,"source":"dbSNP","id":"rs1049934031","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140614223,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614223,"clinical_significance":[],"seq_region_name":"7","id":"rs1800006289"},{"seq_region_name":"7","id":"rs570226978","clinical_significance":[],"strand":1,"feature_type":"variation","end":140614236,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614236,"source":"dbSNP"},{"start":140614245,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140614245,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1800006497","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140614249,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614249,"clinical_significance":[],"seq_region_name":"7","id":"rs1000618684"},{"source":"dbSNP","start":140614250,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140614250,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs957991355"},{"strand":1,"feature_type":"variation","end":140614256,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614256,"source":"dbSNP","seq_region_name":"7","id":"rs531334183","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614259,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140614259,"seq_region_name":"7","id":"rs186496055","clinical_significance":[]},{"seq_region_name":"7","id":"rs1800007113","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140614264,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614264,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1800007211","clinical_significance":[],"start":140614265,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140614265,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"alleles":["C","A"],"end":140614268,"strand":1,"feature_type":"variation","start":140614268,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs562968325","clinical_significance":[]},{"seq_region_name":"7","id":"rs1024874196","clinical_significance":[],"start":140614278,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140614278,"strand":1,"feature_type":"variation"},{"start":140614289,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C"],"end":140614289,"strand":1,"feature_type":"variation","id":"rs945603976","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1192958818","clinical_significance":[],"strand":1,"feature_type":"variation","end":140614292,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614292,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140614297,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614297,"clinical_significance":[],"seq_region_name":"7","id":"rs970633265"},{"feature_type":"variation","strand":1,"alleles":["TTTT","TTT"],"end":140614301,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614298,"clinical_significance":[],"seq_region_name":"7","id":"rs1563179265"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614300,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140614300,"clinical_significance":[],"seq_region_name":"7","id":"rs982406947"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800007956","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140614307,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614307},{"clinical_significance":[],"seq_region_name":"7","id":"rs1212631131","alleles":["CTCGAACTCCTGGCCTC","CTC"],"end":140614338,"feature_type":"variation","strand":1,"source":"dbSNP","start":140614322,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614323,"feature_type":"variation","strand":1,"alleles":["T","-"],"end":140614323,"clinical_significance":[],"id":"rs1800008498","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140614324,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614324,"source":"dbSNP","seq_region_name":"7","id":"rs1484482245","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1277371380","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614325,"feature_type":"variation","strand":1,"end":140614325,"alleles":["G","A"]},{"start":140614325,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["GAACTCCTGGCCT","-"],"end":140614337,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1800008730","clinical_significance":[]},{"seq_region_name":"7","id":"rs928095658","clinical_significance":[],"strand":1,"feature_type":"variation","end":140614327,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614327,"source":"dbSNP"},{"source":"dbSNP","start":140614330,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140614330,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1563179281"},{"seq_region_name":"7","id":"rs1800009020","clinical_significance":[],"strand":1,"feature_type":"variation","end":140614333,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614333,"source":"dbSNP"},{"alleles":["C","T"],"end":140614336,"feature_type":"variation","strand":1,"source":"dbSNP","start":140614336,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1800009124"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1214585488","end":140614337,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140614337,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1341392675","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614340,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140614340},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614342,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140614342,"id":"rs1268305619","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130709086","clinical_significance":[],"end":140614343,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140614343,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1218908621","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614344,"feature_type":"variation","strand":1,"end":140614344,"alleles":["A","C","G","T"]},{"strand":1,"feature_type":"variation","end":140614345,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614345,"source":"dbSNP","seq_region_name":"7","id":"rs530393220","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614348,"feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140614348,"clinical_significance":[],"seq_region_name":"7","id":"rs938176463"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614353,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140614353,"clinical_significance":[],"seq_region_name":"7","id":"rs1800009817"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614354,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140614354,"seq_region_name":"7","id":"rs2130709119","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800009902","source":"dbSNP","start":140614355,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140614355,"alleles":["T","C"],"feature_type":"variation","strand":1},{"start":140614357,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140614357,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs559219779","clinical_significance":[]},{"id":"rs2130709136","seq_region_name":"7","clinical_significance":[],"start":140614358,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140614358,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800010087","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614359,"feature_type":"variation","strand":1,"end":140614359,"alleles":["C","A"]},{"clinical_significance":[],"id":"rs143713809","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614361,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140614361},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614366,"feature_type":"variation","strand":1,"end":140614366,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs191294270"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130709160","source":"dbSNP","start":140614367,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140614367,"alleles":["A","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130709172","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140614368,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614368},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800010397","alleles":["T","C"],"end":140614369,"feature_type":"variation","strand":1,"source":"dbSNP","start":140614369,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140614371,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140614371,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1413232271","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1800010613","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614374,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140614374},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614375,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140614375,"id":"rs2130709200","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs984210628","source":"dbSNP","start":140614379,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140614379,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs908634601","source":"dbSNP","start":140614382,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140614382,"alleles":["G","A"],"feature_type":"variation","strand":1},{"start":140614384,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140614384,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130709226","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140614385,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614385,"clinical_significance":[],"seq_region_name":"7","id":"rs1563179310"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140614391,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614391,"source":"dbSNP","seq_region_name":"7","id":"rs1800011018","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140614393,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614393,"source":"dbSNP","seq_region_name":"7","id":"rs1800011109","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140614394,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614394,"clinical_significance":[],"seq_region_name":"7","id":"rs898918383"},{"clinical_significance":[],"seq_region_name":"7","id":"rs759033497","source":"dbSNP","start":140614395,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140614395,"alleles":["G","A"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614396,"feature_type":"variation","strand":1,"end":140614396,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1800011433"},{"end":140614398,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140614398,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1800011516"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1047841753","source":"dbSNP","start":140614399,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140614399,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800011695","end":140614401,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140614401,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs553787632","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614407,"feature_type":"variation","strand":1,"end":140614407,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs886135043","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614418,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140614418},{"id":"rs1009206276","seq_region_name":"7","clinical_significance":[],"start":140614426,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140614426,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"id":"rs1420560965","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140614428,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614428,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614435,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","G","T"],"end":140614435,"seq_region_name":"7","id":"rs1800012205","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs922822846","source":"dbSNP","start":140614436,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140614436,"alleles":["T","G"],"feature_type":"variation","strand":1},{"end":140614440,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140614440,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130709301"},{"start":140614441,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140614441,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1800012444","clinical_significance":[]},{"end":140614444,"alleles":["A","-"],"strand":1,"feature_type":"variation","start":140614444,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1800012562","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800012663","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140614446,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614446},{"id":"rs1201779829","seq_region_name":"7","clinical_significance":[],"start":140614447,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140614447,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800012862","source":"dbSNP","start":140614448,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140614448,"feature_type":"variation","strand":1},{"end":140614450,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140614450,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1267121205"},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140614452,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614452,"source":"dbSNP","seq_region_name":"7","id":"rs1800013045","clinical_significance":[]},{"seq_region_name":"7","id":"rs1432373058","clinical_significance":[],"alleles":["C","T"],"end":140614453,"strand":1,"feature_type":"variation","start":140614453,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140614455,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614455,"source":"dbSNP","id":"rs1585759341","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1800013303","clinical_significance":[],"end":140614457,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140614457,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140614460,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140614460,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1800013394","clinical_significance":[]},{"source":"dbSNP","start":140614463,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140614463,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1800013483"},{"strand":1,"feature_type":"variation","end":140614468,"alleles":["AAAA","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614465,"source":"dbSNP","seq_region_name":"7","id":"rs1438994413","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614473,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140614473,"clinical_significance":[],"seq_region_name":"7","id":"rs1182324277"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614474,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140614474,"id":"rs1800013806","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1018829862","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614489,"feature_type":"variation","strand":1,"end":140614489,"alleles":["G","C"]},{"strand":1,"feature_type":"variation","alleles":["GC","-"],"end":140614493,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614492,"source":"dbSNP","id":"rs1800013992","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614493,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140614493,"clinical_significance":[],"seq_region_name":"7","id":"rs932897676"},{"seq_region_name":"7","id":"rs1800014170","clinical_significance":[],"start":140614497,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140614497,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140614500,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614500,"source":"dbSNP","seq_region_name":"7","id":"rs1050470420","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563179349","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614506,"feature_type":"variation","strand":1,"end":140614506,"alleles":["T","C"]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140614514,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614514,"clinical_significance":[],"id":"rs1800014666","seq_region_name":"7"},{"end":140614518,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140614518,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1451493915"},{"seq_region_name":"7","id":"rs926123058","clinical_significance":[],"alleles":["A","C"],"end":140614524,"strand":1,"feature_type":"variation","start":140614524,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140614526,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614526,"clinical_significance":[],"id":"rs1231156614","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1378760492","feature_type":"variation","strand":1,"end":140614550,"alleles":["ATTACATATTCATAAAATTACAT","ATTACAT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614528},{"clinical_significance":[],"seq_region_name":"7","id":"rs936194232","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614533,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140614533},{"end":140614538,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140614538,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1365595347","clinical_significance":[]},{"seq_region_name":"7","id":"rs1800015754","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614550,"source":"dbSNP","strand":1,"feature_type":"variation","end":140614550,"alleles":["T","C"]},{"start":140614555,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140614555,"strand":1,"feature_type":"variation","id":"rs900308866","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1053512337","source":"dbSNP","start":140614556,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140614556,"feature_type":"variation","strand":1},{"alleles":["ATA","A"],"end":140614558,"strand":1,"feature_type":"variation","start":140614556,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs568361964","seq_region_name":"7","clinical_significance":[]},{"end":140614557,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140614557,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1563179368","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1563179370","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140614567,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614567,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614568,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140614568,"clinical_significance":[],"seq_region_name":"7","id":"rs1800016505"},{"seq_region_name":"7","id":"rs1462479803","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614569,"source":"dbSNP","strand":1,"feature_type":"variation","end":140614569,"alleles":["T","A"]},{"alleles":["A","C"],"end":140614572,"feature_type":"variation","strand":1,"source":"dbSNP","start":140614572,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1800016787"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130709490","alleles":["A","G"],"end":140614574,"feature_type":"variation","strand":1,"source":"dbSNP","start":140614574,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140614578,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140614578,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1397248669","clinical_significance":[]},{"source":"dbSNP","start":140614580,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140614580,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1800017098"},{"seq_region_name":"7","id":"rs1163225516","clinical_significance":[],"start":140614582,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140614582,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140614584,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140614584,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1800017430"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140614585,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614585,"source":"dbSNP","id":"rs892238116","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1426005701","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614586,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140614586},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614593,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140614593,"seq_region_name":"7","id":"rs995967779","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140614596,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614596,"source":"dbSNP","seq_region_name":"7","id":"rs1800018042","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800018155","source":"dbSNP","start":140614600,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140614600,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614605,"source":"dbSNP","strand":1,"feature_type":"variation","end":140614605,"alleles":["T","G"],"seq_region_name":"7","id":"rs1046102117","clinical_significance":[]},{"id":"rs1300896201","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140614607,"strand":1,"feature_type":"variation","start":140614607,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs34500694","seq_region_name":"7","source":"dbSNP","start":140614608,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AA","AAA"],"end":140614609,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130709551","source":"dbSNP","start":140614609,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140614609,"alleles":["A","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1585759671","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614611,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140614611},{"source":"dbSNP","start":140614613,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140614613,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1800018846"},{"end":140614631,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140614631,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1800018931"},{"end":140614633,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140614633,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1800019025","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800019108","alleles":["G","A"],"end":140614634,"feature_type":"variation","strand":1,"source":"dbSNP","start":140614634,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614637,"feature_type":"variation","strand":1,"end":140614637,"alleles":["G","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1800019193"},{"strand":1,"feature_type":"variation","end":140614638,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614638,"source":"dbSNP","seq_region_name":"7","id":"rs1177409568","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140614644,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614644,"clinical_significance":[],"id":"rs796251901","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800019517","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614650,"feature_type":"variation","strand":1,"end":140614650,"alleles":["A","G"]},{"feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140614651,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614651,"clinical_significance":[],"id":"rs1032844231","seq_region_name":"7"},{"alleles":["G","A","C"],"end":140614653,"strand":1,"feature_type":"variation","start":140614653,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs958353772","clinical_significance":[]},{"alleles":["A","G"],"end":140614656,"strand":1,"feature_type":"variation","start":140614656,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1800019862","clinical_significance":[]},{"source":"dbSNP","start":140614664,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["ACAACAA","ACAA"],"end":140614670,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1002123096","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130709615","feature_type":"variation","strand":1,"end":140614665,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614665},{"id":"rs183980324","seq_region_name":"7","clinical_significance":[],"start":140614667,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140614667,"strand":1,"feature_type":"variation"},{"alleles":["C","T"],"end":140614668,"feature_type":"variation","strand":1,"source":"dbSNP","start":140614668,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1800020217"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614671,"source":"dbSNP","strand":1,"feature_type":"variation","end":140614671,"alleles":["T","C"],"id":"rs1284663366","seq_region_name":"7","clinical_significance":[]},{"end":140614674,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140614674,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1800020431"},{"clinical_significance":[],"id":"rs1800020523","seq_region_name":"7","end":140614677,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140614677,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585759734","feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140614682,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614682},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800020870","end":140614686,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140614686,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1021353625","seq_region_name":"7","source":"dbSNP","start":140614690,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140614690,"alleles":["G","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1800021211","seq_region_name":"7","source":"dbSNP","start":140614694,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140614694,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585759756","feature_type":"variation","strand":1,"end":140614698,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614698},{"clinical_significance":[],"id":"rs1800021536","seq_region_name":"7","end":140614700,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140614700,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800021685","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140614708,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614708},{"end":140614709,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140614709,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1800021844","clinical_significance":[]},{"alleles":["C","A"],"end":140614712,"feature_type":"variation","strand":1,"source":"dbSNP","start":140614712,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1800021995"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614713,"feature_type":"variation","strand":1,"end":140614713,"alleles":["T","C"],"clinical_significance":[],"id":"rs952549989","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614717,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140614717,"seq_region_name":"7","id":"rs1005819282","clinical_significance":[]},{"seq_region_name":"7","id":"rs1441638014","clinical_significance":[],"end":140614718,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140614718,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["C","T"],"end":140614721,"feature_type":"variation","strand":1,"source":"dbSNP","start":140614721,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1800022674"},{"strand":1,"feature_type":"variation","end":140614722,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614722,"source":"dbSNP","seq_region_name":"7","id":"rs1800022906","clinical_significance":[]},{"seq_region_name":"7","id":"rs1015641304","clinical_significance":[],"alleles":["C","A"],"end":140614726,"strand":1,"feature_type":"variation","start":140614726,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614729,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140614729,"clinical_significance":[],"seq_region_name":"7","id":"rs1800023259"},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140614732,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614732,"clinical_significance":[],"seq_region_name":"7","id":"rs1563179421"},{"seq_region_name":"7","id":"rs1563179423","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614735,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140614735},{"start":140614736,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140614736,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs961450206","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1308210436","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614737,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140614737},{"seq_region_name":"7","id":"rs1800023990","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614744,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140614744},{"seq_region_name":"7","id":"rs1563179425","clinical_significance":[],"end":140614746,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140614746,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140614747,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614747,"clinical_significance":[],"seq_region_name":"7","id":"rs2130709747"},{"seq_region_name":"7","id":"rs1346199968","clinical_significance":[],"start":140614751,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140614751,"strand":1,"feature_type":"variation"},{"alleles":["G","A","C"],"end":140614756,"strand":1,"feature_type":"variation","start":140614756,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1161728229","clinical_significance":[]},{"seq_region_name":"7","id":"rs966756110","clinical_significance":[],"end":140614763,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","start":140614763,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614770,"source":"dbSNP","strand":1,"feature_type":"variation","end":140614770,"alleles":["C","G"],"seq_region_name":"7","id":"rs539274124","clinical_significance":[]},{"seq_region_name":"7","id":"rs1337932629","clinical_significance":[],"start":140614773,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140614773,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140614776,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140614776,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1378030028"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614779,"source":"dbSNP","strand":1,"feature_type":"variation","end":140614779,"alleles":["T","C"],"seq_region_name":"7","id":"rs1157561907","clinical_significance":[]},{"source":"dbSNP","start":140614781,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","TT"],"end":140614781,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1800025138"},{"source":"dbSNP","start":140614783,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140614783,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs982334968"},{"end":140614786,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140614786,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1800025371","seq_region_name":"7"},{"alleles":["A","C","G"],"end":140614788,"feature_type":"variation","strand":1,"source":"dbSNP","start":140614788,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs753202145"},{"seq_region_name":"7","id":"rs1191715449","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614795,"source":"dbSNP","strand":1,"feature_type":"variation","end":140614795,"alleles":["C","G"]},{"alleles":["T","-"],"end":140614802,"strand":1,"feature_type":"variation","start":140614802,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1488116038","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs959489938","seq_region_name":"7","source":"dbSNP","start":140614805,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140614805,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs990984527","clinical_significance":[],"end":140614810,"alleles":["T","C","G"],"strand":1,"feature_type":"variation","start":140614810,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140614818,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140614818,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1285936070"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800026055","feature_type":"variation","strand":1,"alleles":["T","A"],"end":140614822,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614822},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614827,"source":"dbSNP","strand":1,"feature_type":"variation","end":140614827,"alleles":["G","A"],"seq_region_name":"7","id":"rs1800026157","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1315351541","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140614830,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614830},{"clinical_significance":[],"id":"rs1285524985","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614833,"feature_type":"variation","strand":1,"end":140614833,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1235140337","alleles":["C","T"],"end":140614838,"feature_type":"variation","strand":1,"source":"dbSNP","start":140614838,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1800026644","clinical_significance":[],"start":140614859,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140614859,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs920798166","clinical_significance":[],"strand":1,"feature_type":"variation","end":140614867,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614867,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1350206732","feature_type":"variation","strand":1,"alleles":["AAAAA","AAA"],"end":140614872,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614868},{"id":"rs930375400","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614872,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140614872},{"clinical_significance":[],"seq_region_name":"7","id":"rs1224894496","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614873,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140614873},{"seq_region_name":"7","id":"rs954069717","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614873,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TTTTTTTTT","TTTTTTTT","TTTTTTTTTT"],"end":140614881},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140614886,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614886,"clinical_significance":[],"seq_region_name":"7","id":"rs1800027318"},{"seq_region_name":"7","id":"rs1291006468","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140614890,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614890,"source":"dbSNP"},{"clinical_significance":[],"id":"rs985716293","seq_region_name":"7","source":"dbSNP","start":140614898,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140614898,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1800027514","seq_region_name":"7","feature_type":"variation","strand":1,"end":140614899,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614899},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800027662","alleles":["C","T"],"end":140614900,"feature_type":"variation","strand":1,"source":"dbSNP","start":140614900,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614903,"source":"dbSNP","strand":1,"feature_type":"variation","end":140614903,"alleles":["G","A"],"seq_region_name":"7","id":"rs1358258166","clinical_significance":[]},{"start":140614909,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140614909,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1800027867","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614910,"source":"dbSNP","strand":1,"feature_type":"variation","end":140614910,"alleles":["T","A"],"seq_region_name":"7","id":"rs1488303958","clinical_significance":[]},{"id":"rs1047498116","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140614912,"strand":1,"feature_type":"variation","start":140614912,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140614919,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614919,"clinical_significance":[],"seq_region_name":"7","id":"rs907503215"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614922,"feature_type":"variation","strand":1,"end":140614922,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130709900"},{"end":140614923,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140614923,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1196637732"},{"alleles":["C","G"],"end":140614926,"feature_type":"variation","strand":1,"source":"dbSNP","start":140614926,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1800028615","seq_region_name":"7"},{"clinical_significance":[],"id":"rs761327543","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140614942,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614942},{"strand":1,"feature_type":"variation","end":140614943,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614943,"source":"dbSNP","seq_region_name":"7","id":"rs1173331829","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140614945,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614945,"clinical_significance":[],"seq_region_name":"7","id":"rs1417093706"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140614948,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614948,"source":"dbSNP","seq_region_name":"7","id":"rs1563179524","clinical_significance":[]},{"id":"rs926210340","seq_region_name":"7","clinical_significance":[],"start":140614955,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140614955,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs371297044","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614963,"feature_type":"variation","strand":1,"end":140614963,"alleles":["A","G"]},{"start":140614971,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140614971,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1800029715","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800029816","alleles":["C","T"],"end":140614972,"feature_type":"variation","strand":1,"source":"dbSNP","start":140614972,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs936159328","end":140614973,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140614973,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs989386765","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614975,"source":"dbSNP","strand":1,"feature_type":"variation","end":140614975,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs558021023","clinical_significance":[],"strand":1,"feature_type":"variation","end":140614979,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614979,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614981,"source":"dbSNP","strand":1,"feature_type":"variation","end":140614981,"alleles":["C","T"],"id":"rs1800030281","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","A","T"],"end":140614986,"strand":1,"feature_type":"variation","start":140614986,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs576280245","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614987,"feature_type":"variation","strand":1,"end":140614987,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs944395149"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563179542","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614988,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140614988},{"feature_type":"variation","strand":1,"end":140614994,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140614994,"clinical_significance":[],"seq_region_name":"7","id":"rs1800030748"},{"strand":1,"feature_type":"variation","end":140614995,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614995,"source":"dbSNP","seq_region_name":"7","id":"rs1800030854","clinical_significance":[]},{"alleles":["G","T"],"end":140614997,"feature_type":"variation","strand":1,"source":"dbSNP","start":140614997,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1348907900"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140614998,"source":"dbSNP","strand":1,"feature_type":"variation","end":140614998,"alleles":["C","G","T"],"seq_region_name":"7","id":"rs1462140514","clinical_significance":[]},{"seq_region_name":"7","id":"rs754270410","clinical_significance":[],"start":140614999,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140614999,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs6964929","clinical_significance":[],"start":140615006,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140615006,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140615007,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140615007,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs900423531","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615008,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140615008,"seq_region_name":"7","id":"rs1800031543","clinical_significance":[]},{"seq_region_name":"7","id":"rs757400635","clinical_significance":[],"strand":1,"feature_type":"variation","end":140615012,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615012,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140615015,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615015,"source":"dbSNP","seq_region_name":"7","id":"rs1800031771","clinical_significance":[]},{"seq_region_name":"7","id":"rs1800031870","clinical_significance":[],"start":140615019,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140615019,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615020,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140615020,"clinical_significance":[],"seq_region_name":"7","id":"rs1800031957"},{"strand":1,"feature_type":"variation","end":140615021,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615021,"source":"dbSNP","seq_region_name":"7","id":"rs1294290523","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800032157","alleles":["A","G"],"end":140615022,"feature_type":"variation","strand":1,"source":"dbSNP","start":140615022,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1415083838","clinical_significance":[],"start":140615023,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140615023,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs555885700","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140615024,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615024},{"source":"dbSNP","start":140615030,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140615030,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1800032514"},{"seq_region_name":"7","id":"rs115488851","clinical_significance":[],"start":140615039,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140615039,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615042,"feature_type":"variation","strand":1,"end":140615047,"alleles":["TTTTTT","TTTTTTT"],"clinical_significance":[],"seq_region_name":"7","id":"rs906178781"},{"clinical_significance":[],"id":"rs1465070998","seq_region_name":"7","feature_type":"variation","strand":1,"end":140615046,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615046},{"clinical_significance":[],"seq_region_name":"7","id":"rs1445119042","source":"dbSNP","start":140615050,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140615050,"alleles":["C","G","T"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615051,"feature_type":"variation","strand":1,"end":140615051,"alleles":["G","A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs570484042"},{"end":140615052,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140615052,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1011383275","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140615053,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615053,"clinical_significance":[],"seq_region_name":"7","id":"rs1585760364"},{"source":"dbSNP","start":140615055,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140615055,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs937688356","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615057,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140615057,"clinical_significance":[],"id":"rs2130710088","seq_region_name":"7"},{"clinical_significance":[],"id":"rs2130710100","seq_region_name":"7","source":"dbSNP","start":140615058,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140615058,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs2130710106","clinical_significance":[],"start":140615059,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140615059,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1800033592","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615063,"feature_type":"variation","strand":1,"end":140615063,"alleles":["C","T"]},{"source":"dbSNP","start":140615070,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140615070,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1800033700"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615073,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140615073,"seq_region_name":"7","id":"rs1055029495","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1254293558","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615074,"feature_type":"variation","strand":1,"end":140615074,"alleles":["C","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615077,"feature_type":"variation","strand":1,"end":140615077,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1800034172"},{"clinical_significance":[],"seq_region_name":"7","id":"rs534704232","feature_type":"variation","strand":1,"end":140615086,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615086},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140615087,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615087,"clinical_significance":[],"id":"rs1005353750","seq_region_name":"7"},{"start":140615090,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G","T"],"end":140615090,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1253120963","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615091,"feature_type":"variation","strand":1,"end":140615091,"alleles":["T","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1310620703"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1015374019","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615094,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140615094},{"start":140615100,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140615100,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1274215528","clinical_significance":[]},{"alleles":["A","T"],"end":140615101,"strand":1,"feature_type":"variation","start":140615101,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1800035688","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585760450","source":"dbSNP","start":140615105,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140615105,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800035980","alleles":["C","T"],"end":140615106,"feature_type":"variation","strand":1,"source":"dbSNP","start":140615106,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1800036125","clinical_significance":[],"end":140615111,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140615111,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs897033720","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140615112,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615112,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1800036444","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615114,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140615114},{"id":"rs1205419582","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140615119,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615119,"source":"dbSNP"},{"start":140615120,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140615120,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs1800036649","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs967080917","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140615122,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615122,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1800036856","clinical_significance":[],"strand":1,"feature_type":"variation","end":140615123,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615123,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1395064573","alleles":["G","A","T"],"end":140615130,"feature_type":"variation","strand":1,"source":"dbSNP","start":140615130,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140615133,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615133,"clinical_significance":[],"seq_region_name":"7","id":"rs1029729591"},{"alleles":["T","C","G"],"end":140615134,"feature_type":"variation","strand":1,"source":"dbSNP","start":140615134,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1253296749"},{"seq_region_name":"7","id":"rs1003550235","clinical_significance":[],"start":140615138,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C","G"],"end":140615138,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615139,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140615139,"clinical_significance":[],"id":"rs1800037453","seq_region_name":"7"},{"seq_region_name":"7","id":"rs954042303","clinical_significance":[],"start":140615142,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140615142,"strand":1,"feature_type":"variation"},{"alleles":["A","G"],"end":140615143,"strand":1,"feature_type":"variation","start":140615143,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1585760534","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","A"],"end":140615145,"feature_type":"variation","strand":1,"source":"dbSNP","start":140615145,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1800037766","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615146,"feature_type":"variation","strand":1,"end":140615146,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1462776509"},{"seq_region_name":"7","id":"rs563250022","clinical_significance":[],"start":140615147,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140615147,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1800038084","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140615149,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615149,"source":"dbSNP"},{"alleles":["A","G"],"end":140615150,"strand":1,"feature_type":"variation","start":140615150,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1800038197","seq_region_name":"7","clinical_significance":[]},{"start":140615152,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140615152,"alleles":["C","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1033226394","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615156,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140615156,"seq_region_name":"7","id":"rs1800038426","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140615160,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615160,"source":"dbSNP","id":"rs959603393","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615163,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140615163,"clinical_significance":[],"seq_region_name":"7","id":"rs1800038739"},{"id":"rs1563179639","seq_region_name":"7","clinical_significance":[],"end":140615165,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140615165,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140615169,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140615169,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1800039048"},{"alleles":["G","T"],"end":140615175,"feature_type":"variation","strand":1,"source":"dbSNP","start":140615175,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs991100599","seq_region_name":"7"},{"start":140615175,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["GG","G"],"end":140615176,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1800039356","clinical_significance":[]},{"start":140615176,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140615176,"alleles":["G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1800039528","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615181,"source":"dbSNP","strand":1,"feature_type":"variation","end":140615181,"alleles":["A","T"],"seq_region_name":"7","id":"rs1479531905","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615186,"source":"dbSNP","strand":1,"feature_type":"variation","end":140615186,"alleles":["A","G"],"seq_region_name":"7","id":"rs1419895219","clinical_significance":[]},{"id":"rs1252827927","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140615188,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615188,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140615196,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615196,"source":"dbSNP","seq_region_name":"7","id":"rs1800040183","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585760609","source":"dbSNP","start":140615197,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140615197,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1800040553","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615200,"source":"dbSNP","strand":1,"feature_type":"variation","end":140615200,"alleles":["G","T"]},{"strand":1,"feature_type":"variation","end":140615202,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615202,"source":"dbSNP","seq_region_name":"7","id":"rs1800040738","clinical_significance":[]},{"start":140615208,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140615208,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1197837464","clinical_significance":[]},{"seq_region_name":"7","id":"rs920743038","clinical_significance":[],"start":140615212,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140615212,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615214,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140615214,"id":"rs138953101","seq_region_name":"7","clinical_significance":[]},{"start":140615215,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140615215,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1800041179","clinical_significance":[]},{"id":"rs545275355","seq_region_name":"7","clinical_significance":[],"alleles":["A","C"],"end":140615217,"strand":1,"feature_type":"variation","start":140615217,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140615218,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615218,"source":"dbSNP","seq_region_name":"7","id":"rs2130710348","clinical_significance":[]},{"id":"rs1800041385","seq_region_name":"7","clinical_significance":[],"start":140615220,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140615222,"alleles":["TTT","T"],"strand":1,"feature_type":"variation"},{"id":"rs1215964239","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["TTTATTTATTTAT","TTTATTTAT"],"end":140615232,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615220,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615237,"feature_type":"variation","strand":1,"end":140615237,"alleles":["T","A","C"],"clinical_significance":[],"id":"rs1207561169","seq_region_name":"7"},{"alleles":["C","A","T"],"end":140615239,"strand":1,"feature_type":"variation","start":140615239,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1412380974","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140615240,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615240,"clinical_significance":[],"seq_region_name":"7","id":"rs1585760692"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615243,"feature_type":"variation","strand":1,"end":140615243,"alleles":["A","G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1800041943"},{"start":140615244,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140615244,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1800042128","clinical_significance":[]},{"seq_region_name":"7","id":"rs983571149","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615246,"source":"dbSNP","strand":1,"feature_type":"variation","end":140615246,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1428606267","clinical_significance":[],"strand":1,"feature_type":"variation","end":140615259,"alleles":["AAA","AA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615257,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs989108629","end":140615261,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140615261,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["T","-"],"end":140615264,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615264,"clinical_significance":[],"seq_region_name":"7","id":"rs1443848909"},{"seq_region_name":"7","id":"rs1800042527","clinical_significance":[],"end":140615273,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140615273,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1800042619","seq_region_name":"7","alleles":["A","G"],"end":140615282,"feature_type":"variation","strand":1,"source":"dbSNP","start":140615282,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1376095783","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615286,"source":"dbSNP","strand":1,"feature_type":"variation","end":140615286,"alleles":["C","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800042802","source":"dbSNP","start":140615287,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140615290,"alleles":["AGAG","AG"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615288,"source":"dbSNP","strand":1,"feature_type":"variation","end":140615288,"alleles":["G","C"],"seq_region_name":"7","id":"rs1800042880","clinical_significance":[]},{"source":"dbSNP","start":140615294,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140615294,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1326555770"},{"source":"dbSNP","start":140615299,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140615299,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1442971604"},{"clinical_significance":[],"seq_region_name":"7","id":"rs907620352","end":140615301,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140615301,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615302,"feature_type":"variation","strand":1,"end":140615302,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1162422114"},{"clinical_significance":[],"id":"rs1585760759","seq_region_name":"7","source":"dbSNP","start":140615305,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140615305,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800043360","source":"dbSNP","start":140615306,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140615306,"alleles":["G","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs2130710453","clinical_significance":[],"strand":1,"feature_type":"variation","end":140615308,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615308,"source":"dbSNP"},{"end":140615310,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140615310,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1454519500","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140615327,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615327,"source":"dbSNP","seq_region_name":"7","id":"rs1365690268","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140615330,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615330,"source":"dbSNP","id":"rs2130710471","seq_region_name":"7","clinical_significance":[]},{"start":140615333,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140615333,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs1800043654","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585760789","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615335,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140615335},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800043859","source":"dbSNP","start":140615339,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140615339,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615344,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AACAACA","AACA"],"end":140615350,"seq_region_name":"7","id":"rs1800043951","clinical_significance":[]},{"source":"dbSNP","start":140615346,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140615346,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1156966834"},{"clinical_significance":[],"seq_region_name":"7","id":"rs563587195","feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140615352,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615352},{"end":140615353,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140615353,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs531000335","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1450386760","source":"dbSNP","start":140615355,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140615355,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs921629303","clinical_significance":[],"start":140615357,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C","T"],"end":140615357,"strand":1,"feature_type":"variation"},{"alleles":["C","T"],"end":140615359,"feature_type":"variation","strand":1,"source":"dbSNP","start":140615359,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs931880726"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1267174380","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615360,"feature_type":"variation","strand":1,"end":140615360,"alleles":["A","C","G"]},{"seq_region_name":"7","id":"rs1485992159","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615363,"source":"dbSNP","strand":1,"feature_type":"variation","end":140615363,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1287659882","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615368,"source":"dbSNP","strand":1,"feature_type":"variation","end":140615368,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1237481364","source":"dbSNP","start":140615369,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140615369,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1563179716","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615369,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AAAA","AAAAA"],"end":140615372},{"clinical_significance":[],"seq_region_name":"7","id":"rs1455006991","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615374,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140615374},{"source":"dbSNP","start":140615376,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140615376,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585760898"},{"start":140615377,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140615377,"strand":1,"feature_type":"variation","id":"rs1301623610","seq_region_name":"7","clinical_significance":[]},{"end":140615378,"alleles":["G","C","T"],"strand":1,"feature_type":"variation","start":140615378,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1378439451","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615380,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140615380,"id":"rs1215307196","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140615385,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615385,"source":"dbSNP","seq_region_name":"7","id":"rs1297974140","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140615386,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615386,"source":"dbSNP","seq_region_name":"7","id":"rs1800045878","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140615387,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615387,"source":"dbSNP","seq_region_name":"7","id":"rs1322660534","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800046089","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615390,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140615390},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615394,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140615394,"clinical_significance":[],"seq_region_name":"7","id":"rs981830968"},{"seq_region_name":"7","id":"rs1054316661","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615396,"source":"dbSNP","strand":1,"feature_type":"variation","end":140615396,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1800046400","clinical_significance":[],"alleles":["CC","C"],"end":140615397,"strand":1,"feature_type":"variation","start":140615396,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1585760976","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140615409,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615409,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615413,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140615413,"seq_region_name":"7","id":"rs1800046625","clinical_significance":[]},{"source":"dbSNP","start":140615416,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140615416,"alleles":["T","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs892933334"},{"source":"dbSNP","start":140615418,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140615418,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs549475225"},{"seq_region_name":"7","id":"rs1316344275","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","-"],"end":140615420,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615420,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615420,"source":"dbSNP","strand":1,"feature_type":"variation","end":140615420,"alleles":["C","T"],"seq_region_name":"7","id":"rs1585760997","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615425,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140615425,"clinical_significance":[],"seq_region_name":"7","id":"rs1800047135"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1010080465","source":"dbSNP","start":140615426,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140615426,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1042829667","feature_type":"variation","strand":1,"end":140615429,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615429},{"clinical_significance":[],"id":"rs530724383","seq_region_name":"7","end":140615430,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140615430,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615434,"source":"dbSNP","strand":1,"feature_type":"variation","end":140615434,"alleles":["A","T"],"seq_region_name":"7","id":"rs1800047488","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615445,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140615445,"clinical_significance":[],"seq_region_name":"7","id":"rs1585761024"},{"alleles":["ACGAC","AC"],"end":140615454,"feature_type":"variation","strand":1,"source":"dbSNP","start":140615450,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1800047677"},{"strand":1,"feature_type":"variation","end":140615451,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615451,"source":"dbSNP","id":"rs567772415","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs142950926","source":"dbSNP","start":140615452,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140615452,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615458,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140615458,"clinical_significance":[],"id":"rs1800048044","seq_region_name":"7"},{"end":140615459,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140615459,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs112005719","clinical_significance":[]},{"start":140615461,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140615461,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1800048253","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1377493930","feature_type":"variation","strand":1,"end":140615465,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615465},{"seq_region_name":"7","id":"rs1194382254","clinical_significance":[],"end":140615470,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140615470,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140615477,"alleles":["C","A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615477,"clinical_significance":[],"seq_region_name":"7","id":"rs1800048556"},{"seq_region_name":"7","id":"rs1449147798","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615483,"source":"dbSNP","strand":1,"feature_type":"variation","end":140615483,"alleles":["C","T"]},{"start":140615488,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140615488,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs941272805","clinical_significance":[]},{"alleles":["T","C","G"],"end":140615489,"strand":1,"feature_type":"variation","start":140615489,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs565525744","clinical_significance":[]},{"id":"rs539747147","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615502,"source":"dbSNP","strand":1,"feature_type":"variation","end":140615502,"alleles":["A","G"]},{"end":140615503,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140615503,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585761097"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615504,"source":"dbSNP","strand":1,"feature_type":"variation","end":140615504,"alleles":["C","A","G"],"seq_region_name":"7","id":"rs144683982","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1342825587","source":"dbSNP","start":140615506,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140615506,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615508,"source":"dbSNP","strand":1,"feature_type":"variation","end":140615508,"alleles":["G","T"],"id":"rs2130710736","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs36016210","clinical_significance":[],"strand":1,"feature_type":"variation","end":140615510,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615510,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1027913076","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615513,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140615513},{"seq_region_name":"7","id":"rs1800049642","clinical_significance":[],"start":140615514,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140615514,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"alleles":["AGGAG","AG"],"end":140615526,"strand":1,"feature_type":"variation","start":140615522,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1274130313","clinical_significance":[]},{"id":"rs1800049725","seq_region_name":"7","clinical_significance":[],"start":140615524,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140615524,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs952270715","source":"dbSNP","start":140615526,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140615526,"feature_type":"variation","strand":1},{"id":"rs1800049939","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615529,"source":"dbSNP","strand":1,"feature_type":"variation","end":140615529,"alleles":["C","A"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615531,"feature_type":"variation","strand":1,"end":140615531,"alleles":["G","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1800050041"},{"start":140615532,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140615532,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1800050155","clinical_significance":[]},{"source":"dbSNP","start":140615532,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["CTT","-"],"end":140615534,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1228032738"},{"strand":1,"feature_type":"variation","end":140615533,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615533,"source":"dbSNP","id":"rs1800050361","seq_region_name":"7","clinical_significance":[]},{"end":140615548,"alleles":["TTTTTTTTTTTTTTTT","TTTTTTTTTTTT","TTTTTTTTTTTTT","TTTTTTTTTTTTTT","TTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTTTTTTTTTT"],"strand":1,"feature_type":"variation","start":140615533,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs57498403","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140615534,"alleles":["T","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615534,"clinical_significance":[],"id":"rs75824622","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615535,"feature_type":"variation","strand":1,"alleles":["-","C"],"end":140615534,"clinical_significance":[],"id":"rs1800051101","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1585761193","clinical_significance":[],"start":140615537,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A","C"],"end":140615537,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["TT","TTCTT"],"end":140615538,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615537,"source":"dbSNP","id":"rs997985572","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs58206361","clinical_significance":[],"start":140615538,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","TCT"],"end":140615538,"strand":1,"feature_type":"variation"},{"start":140615539,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140615539,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs983634916","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1422004783","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615540,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140615540},{"alleles":["T","A","C"],"end":140615541,"feature_type":"variation","strand":1,"source":"dbSNP","start":140615541,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1015541524"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615543,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140615543,"clinical_significance":[],"id":"rs965752201","seq_region_name":"7"},{"alleles":["T","TCT"],"end":140615543,"feature_type":"variation","strand":1,"source":"dbSNP","start":140615543,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1800052026"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800052134","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615544,"feature_type":"variation","strand":1,"alleles":["-","C"],"end":140615543},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615544,"source":"dbSNP","strand":1,"feature_type":"variation","end":140615544,"alleles":["T","C","G"],"id":"rs975824736","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1257734135","end":140615545,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140615545,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140615545,"alleles":["-","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615546,"clinical_significance":[],"seq_region_name":"7","id":"rs1800052491"},{"end":140615546,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140615546,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1800052593"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585761286","end":140615548,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140615548,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs371321149","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615549,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140615549},{"start":140615549,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140615549,"alleles":["C","-"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1477270226","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615549,"feature_type":"variation","strand":1,"alleles":["C","CC"],"end":140615549,"clinical_significance":[],"id":"rs1800052906","seq_region_name":"7"},{"id":"rs1430350190","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140615550,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615550,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800053186","alleles":["T","G"],"end":140615551,"feature_type":"variation","strand":1,"source":"dbSNP","start":140615551,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140615552,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615552,"clinical_significance":[],"seq_region_name":"7","id":"rs1800053277"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1471164986","feature_type":"variation","strand":1,"end":140615556,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615556},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615557,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140615557,"seq_region_name":"7","id":"rs1174566406","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800053616","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615559,"feature_type":"variation","strand":1,"end":140615559,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs56942922","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615560,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140615560},{"alleles":["G","A"],"end":140615561,"strand":1,"feature_type":"variation","start":140615561,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs537200049","seq_region_name":"7","clinical_significance":[]},{"end":140615563,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140615563,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585761342"},{"source":"dbSNP","start":140615564,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140615564,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1217716890"},{"seq_region_name":"7","id":"rs1585761368","clinical_significance":[],"strand":1,"feature_type":"variation","end":140615565,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615565,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1033415984","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140615568,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615568},{"clinical_significance":[],"seq_region_name":"7","id":"rs931661403","feature_type":"variation","strand":1,"end":140615569,"alleles":["G","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615569},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615570,"feature_type":"variation","strand":1,"end":140615570,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1290748471"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1446051736","source":"dbSNP","start":140615573,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140615573,"alleles":["T","C","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800054785","source":"dbSNP","start":140615575,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140615575,"alleles":["T","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1338558495","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615576,"source":"dbSNP","strand":1,"feature_type":"variation","end":140615576,"alleles":["C","T"]},{"start":140615577,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140615577,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs957431237","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615580,"source":"dbSNP","strand":1,"feature_type":"variation","end":140615580,"alleles":["C","A"],"seq_region_name":"7","id":"rs990441654","clinical_significance":[]},{"clinical_significance":[],"id":"rs1467658105","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615582,"feature_type":"variation","strand":1,"end":140615582,"alleles":["G","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1010472593","alleles":["CA","-"],"end":140615586,"feature_type":"variation","strand":1,"source":"dbSNP","start":140615585,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140615586,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140615586,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1800055418"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615591,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140615591,"id":"rs1585761472","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140615593,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615593,"source":"dbSNP","id":"rs1800055627","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140615597,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615597,"clinical_significance":[],"seq_region_name":"7","id":"rs1800055717"},{"source":"dbSNP","start":140615602,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140615602,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1170454321"},{"seq_region_name":"7","id":"rs1020576432","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615604,"source":"dbSNP","strand":1,"feature_type":"variation","end":140615604,"alleles":["C","T"]},{"end":140615609,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140615609,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs555900075"},{"seq_region_name":"7","id":"rs1420451121","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615614,"source":"dbSNP","strand":1,"feature_type":"variation","end":140615614,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1183274278","end":140615615,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140615615,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs188713311","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615618,"source":"dbSNP","strand":1,"feature_type":"variation","end":140615618,"alleles":["G","A","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615621,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140615621,"seq_region_name":"7","id":"rs2130711046","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140615624,"alleles":["A","C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615624,"clinical_significance":[],"id":"rs1284176613","seq_region_name":"7"},{"end":140615625,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140615625,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1800056562"},{"end":140615626,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140615626,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1236443962"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140615629,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615629,"clinical_significance":[],"seq_region_name":"7","id":"rs1800056770"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615638,"feature_type":"variation","strand":1,"end":140615638,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1800056863"},{"seq_region_name":"7","id":"rs1800056955","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615639,"source":"dbSNP","strand":1,"feature_type":"variation","end":140615639,"alleles":["G","A"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615641,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140615641,"clinical_significance":[],"id":"rs2130711073","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140615642,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615642,"source":"dbSNP","id":"rs570390132","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615643,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","TTCT"],"end":140615643,"id":"rs2130711090","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140615647,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140615647,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1800057169","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1217322684","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615649,"source":"dbSNP","strand":1,"feature_type":"variation","end":140615649,"alleles":["C","G","T"]},{"seq_region_name":"7","id":"rs1800057415","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615651,"source":"dbSNP","strand":1,"feature_type":"variation","end":140615651,"alleles":["C","T"]},{"clinical_significance":[],"id":"rs534722285","seq_region_name":"7","feature_type":"variation","strand":1,"end":140615654,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615654},{"id":"rs1197802596","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140615659,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615659,"source":"dbSNP"},{"end":140615662,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140615662,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1335289369","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1277804214","seq_region_name":"7","feature_type":"variation","strand":1,"end":140615663,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615663},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615665,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140615665,"id":"rs1226879759","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1041546660","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615666,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140615666},{"seq_region_name":"7","id":"rs1800058118","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615673,"source":"dbSNP","strand":1,"feature_type":"variation","end":140615673,"alleles":["T","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1280217936","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615674,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140615674},{"end":140615675,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140615675,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1800058312","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1449039768","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615681,"source":"dbSNP","strand":1,"feature_type":"variation","end":140615681,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs553365863","end":140615684,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140615684,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs141917710","feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140615685,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615685},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585761645","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615686,"feature_type":"variation","strand":1,"end":140615686,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585761660","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615687,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140615687},{"id":"rs990624290","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140615688,"strand":1,"feature_type":"variation","start":140615688,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs965720302","clinical_significance":[],"start":140615690,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140615690,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140615692,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140615692,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs909522206"},{"end":140615698,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140615698,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2908239","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1487685215","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615699,"feature_type":"variation","strand":1,"end":140615699,"alleles":["G","A"]},{"id":"rs545336859","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140615700,"strand":1,"feature_type":"variation","start":140615700,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1270677400","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140615704,"alleles":["TAT","TATAT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615702,"source":"dbSNP"},{"alleles":["A","G","T"],"end":140615703,"strand":1,"feature_type":"variation","start":140615703,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs770652310","clinical_significance":[]},{"clinical_significance":[],"id":"rs1800059828","seq_region_name":"7","feature_type":"variation","strand":1,"end":140615704,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615704},{"alleles":["TTTTTTTTTTTT","TTTTTTTTTT","TTTTTTTTTTT","TTTTTTTTTTTTT","TTTTTTTTTTTTTT"],"end":140615715,"strand":1,"feature_type":"variation","start":140615704,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1248258291","clinical_significance":[]},{"seq_region_name":"7","id":"rs1219030019","clinical_significance":[],"start":140615705,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A","G"],"end":140615705,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1563179965","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615709,"source":"dbSNP","strand":1,"feature_type":"variation","end":140615728,"alleles":["TTTTTTTGTATTTTTTTGTA","TTTTTTTGTA"]},{"id":"rs1481614399","seq_region_name":"7","clinical_significance":[],"end":140615710,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140615710,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1285162049","seq_region_name":"7","feature_type":"variation","strand":1,"end":140615714,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615714},{"seq_region_name":"7","id":"rs78913551","clinical_significance":[],"strand":1,"feature_type":"variation","end":140615715,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615715,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1189885975","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140615716,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615716},{"clinical_significance":[],"seq_region_name":"7","id":"rs1351655021","feature_type":"variation","strand":1,"end":140615717,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615717},{"seq_region_name":"7","id":"rs1425039688","clinical_significance":[],"alleles":["A","T"],"end":140615718,"strand":1,"feature_type":"variation","start":140615718,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1800060678","clinical_significance":[],"alleles":["T","C"],"end":140615719,"strand":1,"feature_type":"variation","start":140615719,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1800060762","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615719,"source":"dbSNP","strand":1,"feature_type":"variation","end":140615725,"alleles":["TTTTTTT","TTTTTT"]},{"alleles":["G","GG"],"end":140615726,"feature_type":"variation","strand":1,"source":"dbSNP","start":140615726,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1308616391","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1401753609","end":140615726,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140615726,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140615732,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615732,"source":"dbSNP","seq_region_name":"7","id":"rs1800061048","clinical_significance":[]},{"seq_region_name":"7","id":"rs1800061133","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615734,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140615734},{"id":"rs1800061216","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140615736,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615736,"source":"dbSNP"},{"source":"dbSNP","start":140615742,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140615742,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1235739797"},{"source":"dbSNP","start":140615744,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140615744,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1370285113"},{"seq_region_name":"7","id":"rs1292148811","clinical_significance":[],"alleles":["TTTT","TTTTT"],"end":140615749,"strand":1,"feature_type":"variation","start":140615746,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1436157392","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140615753,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615753,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140615754,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615754,"clinical_significance":[],"id":"rs1161941465","seq_region_name":"7"},{"id":"rs895112852","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615755,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140615755},{"clinical_significance":[],"id":"rs1800061893","seq_region_name":"7","feature_type":"variation","strand":1,"end":140615756,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615756},{"clinical_significance":[],"seq_region_name":"7","id":"rs61324665","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615760,"feature_type":"variation","strand":1,"end":140615760,"alleles":["C","A"]},{"end":140615761,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140615761,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1050892520","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615766,"source":"dbSNP","strand":1,"feature_type":"variation","end":140615766,"alleles":["T","C"],"id":"rs1800062215","seq_region_name":"7","clinical_significance":[]},{"end":140615767,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140615767,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1800062304","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1419175872","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615768,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140615768},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130711348","source":"dbSNP","start":140615779,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140615779,"feature_type":"variation","strand":1},{"id":"rs1303970763","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615783,"source":"dbSNP","strand":1,"feature_type":"variation","end":140615783,"alleles":["G","A"]},{"id":"rs1800062587","seq_region_name":"7","clinical_significance":[],"start":140615785,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140615785,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140615789,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615789,"clinical_significance":[],"id":"rs1800062692","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800062808","source":"dbSNP","start":140615792,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140615792,"alleles":["A","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1347675049","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140615793,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615793},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615797,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140615797,"clinical_significance":[],"seq_region_name":"7","id":"rs1800063009"},{"alleles":["A","C"],"end":140615798,"feature_type":"variation","strand":1,"source":"dbSNP","start":140615798,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1800063163"},{"strand":1,"feature_type":"variation","alleles":["C","A","G","T"],"end":140615801,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615801,"source":"dbSNP","id":"rs889658224","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1242460310","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615803,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140615803},{"end":140615814,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140615814,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1219149005","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615816,"source":"dbSNP","strand":1,"feature_type":"variation","end":140615816,"alleles":["G","A"],"seq_region_name":"7","id":"rs2130711404","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140615818,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615818,"clinical_significance":[],"id":"rs1007381067","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1028109704","feature_type":"variation","strand":1,"end":140615821,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615821},{"clinical_significance":[],"seq_region_name":"7","id":"rs888027635","end":140615822,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140615822,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1800064359","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140615823,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615823},{"start":140615824,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140615824,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1285410764","clinical_significance":[]},{"start":140615828,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140615828,"strand":1,"feature_type":"variation","id":"rs1585762022","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140615830,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615830,"source":"dbSNP","seq_region_name":"7","id":"rs1005572556","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615832,"feature_type":"variation","strand":1,"end":140615832,"alleles":["T","C"],"clinical_significance":[],"id":"rs1800064991","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615836,"source":"dbSNP","strand":1,"feature_type":"variation","end":140615836,"alleles":["A","C"],"seq_region_name":"7","id":"rs1800065150","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615841,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140615841,"seq_region_name":"7","id":"rs1314496081","clinical_significance":[]},{"end":140615842,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140615842,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs192876448"},{"id":"rs1800065687","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140615845,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615845,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1219133941","clinical_significance":[],"strand":1,"feature_type":"variation","end":140615846,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615846,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1800065992","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140615847,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615847,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1363139789","alleles":["C","G","T"],"end":140615853,"feature_type":"variation","strand":1,"source":"dbSNP","start":140615853,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1280476758","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615854,"feature_type":"variation","strand":1,"end":140615854,"alleles":["T","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs575594039","source":"dbSNP","start":140615857,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C","G"],"end":140615857,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["T","TT"],"end":140615858,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615858,"source":"dbSNP","id":"rs1401478393","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140615860,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C","G"],"end":140615860,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1297078750"},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140615868,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615868,"source":"dbSNP","seq_region_name":"7","id":"rs759127740","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800067230","source":"dbSNP","start":140615870,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140615870,"alleles":["T","C"],"feature_type":"variation","strand":1},{"id":"rs1360369810","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140615872,"strand":1,"feature_type":"variation","start":140615872,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615874,"source":"dbSNP","strand":1,"feature_type":"variation","end":140615874,"alleles":["C","T"],"seq_region_name":"7","id":"rs866616231","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1010261231","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615879,"feature_type":"variation","strand":1,"end":140615879,"alleles":["T","C"]},{"clinical_significance":[],"id":"rs771697885","seq_region_name":"7","source":"dbSNP","start":140615881,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140615881,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1020511056","clinical_significance":[],"alleles":["G","A"],"end":140615882,"strand":1,"feature_type":"variation","start":140615882,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615883,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140615883,"clinical_significance":[],"id":"rs975773873","seq_region_name":"7"},{"source":"dbSNP","start":140615896,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140615896,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1262691298"},{"seq_region_name":"7","id":"rs1800068134","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615898,"source":"dbSNP","strand":1,"feature_type":"variation","end":140615898,"alleles":["C","T"]},{"source":"dbSNP","start":140615899,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140615899,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1182541714"},{"end":140615904,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140615904,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs542786706"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130711562","feature_type":"variation","strand":1,"end":140615907,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615907},{"strand":1,"feature_type":"variation","alleles":["AAAA","AA"],"end":140615911,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615908,"source":"dbSNP","id":"rs1003163592","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140615915,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140615915,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1800068814"},{"clinical_significance":[],"id":"rs1034928731","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615917,"feature_type":"variation","strand":1,"end":140615917,"alleles":["C","T"]},{"id":"rs868462920","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615920,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140615920},{"clinical_significance":[],"seq_region_name":"7","id":"rs958926325","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615921,"feature_type":"variation","strand":1,"end":140615923,"alleles":["ACA","-"]},{"clinical_significance":[],"id":"rs989832345","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615922,"feature_type":"variation","strand":1,"end":140615922,"alleles":["C","T"]},{"id":"rs914258334","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615934,"source":"dbSNP","strand":1,"feature_type":"variation","end":140615934,"alleles":["C","T"]},{"end":140615937,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140615937,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs909647450","seq_region_name":"7"},{"seq_region_name":"7","id":"rs945972598","clinical_significance":[],"strand":1,"feature_type":"variation","end":140615938,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615938,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615939,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140615939,"seq_region_name":"7","id":"rs561645406","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs751017699","source":"dbSNP","start":140615941,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140615941,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1222656205","clinical_significance":[],"start":140615943,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140615943,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615947,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140615947,"clinical_significance":[],"seq_region_name":"7","id":"rs1800070849"},{"seq_region_name":"7","id":"rs1800070998","clinical_significance":[],"alleles":["T","TT"],"end":140615947,"strand":1,"feature_type":"variation","start":140615947,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140615948,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615948,"source":"dbSNP","seq_region_name":"7","id":"rs1447213997","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1400856635","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140615956,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615956},{"clinical_significance":[],"id":"rs1800071295","seq_region_name":"7","feature_type":"variation","strand":1,"end":140615963,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615963},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615968,"feature_type":"variation","strand":1,"end":140615968,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1172592966"},{"seq_region_name":"7","id":"rs2130711648","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615971,"source":"dbSNP","strand":1,"feature_type":"variation","end":140615971,"alleles":["A","G"]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140615972,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615972,"source":"dbSNP","seq_region_name":"7","id":"rs2130711653","clinical_significance":[]},{"start":140615978,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140615978,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1800071471","clinical_significance":[]},{"seq_region_name":"7","id":"rs1800071554","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615982,"source":"dbSNP","strand":1,"feature_type":"variation","end":140615982,"alleles":["T","C"]},{"id":"rs1800071655","seq_region_name":"7","clinical_significance":[],"end":140615986,"alleles":["T","C","G"],"strand":1,"feature_type":"variation","start":140615986,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140615988,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140615988,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1800071770"},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140615989,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140615989,"clinical_significance":[],"seq_region_name":"7","id":"rs1585762356"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140615991,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615991,"source":"dbSNP","seq_region_name":"7","id":"rs529021814","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140615994,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140615994,"source":"dbSNP","seq_region_name":"7","id":"rs1585762370","clinical_significance":[]},{"id":"rs1800072110","seq_region_name":"7","clinical_significance":[],"start":140615997,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140615997,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800072211","source":"dbSNP","start":140615999,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140615999,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140616004,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140616004,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs918469494"},{"feature_type":"variation","strand":1,"end":140616011,"alleles":["TAAGT","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616007,"clinical_significance":[],"seq_region_name":"7","id":"rs1800072414"},{"end":140616011,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140616011,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585762391","clinical_significance":[]},{"seq_region_name":"7","id":"rs1223608498","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616016,"source":"dbSNP","strand":1,"feature_type":"variation","end":140616016,"alleles":["G","A"]},{"alleles":["C","G"],"end":140616020,"feature_type":"variation","strand":1,"source":"dbSNP","start":140616020,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1800072726"},{"start":140616024,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140616024,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs933902372","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140616027,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616027,"clinical_significance":[],"id":"rs1800072925","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1800073023","clinical_significance":[],"start":140616028,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140616029,"alleles":["AA","-"],"strand":1,"feature_type":"variation"},{"alleles":["C","T"],"end":140616035,"strand":1,"feature_type":"variation","start":140616035,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1165799413","clinical_significance":[]},{"end":140616040,"alleles":["CACACA","CACA"],"strand":1,"feature_type":"variation","start":140616035,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1800073228","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1425777574","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616042,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140616042},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140616043,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616043,"source":"dbSNP","seq_region_name":"7","id":"rs1800073410","clinical_significance":[]},{"alleles":["G","A"],"end":140616045,"strand":1,"feature_type":"variation","start":140616045,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs547157595","clinical_significance":[]},{"seq_region_name":"7","id":"rs1449551518","clinical_significance":[],"strand":1,"feature_type":"variation","end":140616049,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616049,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1181287855","clinical_significance":[],"end":140616051,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140616051,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1800074135","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616052,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140616052},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616053,"source":"dbSNP","strand":1,"feature_type":"variation","end":140616053,"alleles":["A","G"],"id":"rs559343799","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140616056,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616056,"clinical_significance":[],"seq_region_name":"7","id":"rs1246440877"},{"alleles":["A","C"],"end":140616059,"strand":1,"feature_type":"variation","start":140616059,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs780671545","clinical_significance":[]},{"start":140616060,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140616060,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1800074610","clinical_significance":[]},{"seq_region_name":"7","id":"rs1054917391","clinical_significance":[],"end":140616067,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140616067,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1056522335","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616069,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140616069},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616070,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140616070,"clinical_significance":[],"seq_region_name":"7","id":"rs1800074953"},{"id":"rs1180978828","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140616076,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616076,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1800075179","seq_region_name":"7","source":"dbSNP","start":140616077,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["CC","C"],"end":140616078,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140616080,"alleles":["AA","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616079,"source":"dbSNP","seq_region_name":"7","id":"rs550838276","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1266402706","alleles":["AAT","-"],"end":140616081,"feature_type":"variation","strand":1,"source":"dbSNP","start":140616079,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616084,"source":"dbSNP","strand":1,"feature_type":"variation","end":140616084,"alleles":["T","C"],"seq_region_name":"7","id":"rs1245145246","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140616088,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616088,"clinical_significance":[],"seq_region_name":"7","id":"rs1439142418"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616089,"source":"dbSNP","strand":1,"feature_type":"variation","end":140616089,"alleles":["G","A"],"id":"rs916663566","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616091,"source":"dbSNP","strand":1,"feature_type":"variation","end":140616091,"alleles":["G","T"],"id":"rs1800075842","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs948152108","clinical_significance":[],"end":140616092,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140616092,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140616093,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140616093,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs753294910"},{"start":140616095,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140616095,"alleles":["G","C"],"strand":1,"feature_type":"variation","id":"rs761235915","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1399356779","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616098,"source":"dbSNP","strand":1,"feature_type":"variation","end":140616098,"alleles":["G","T"]},{"seq_region_name":"7","id":"rs1293883048","clinical_significance":[],"alleles":["T","C"],"end":140616104,"strand":1,"feature_type":"variation","start":140616104,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1459645671","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616105,"feature_type":"variation","strand":1,"end":140616105,"alleles":["G","A","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800076618","alleles":["C","T"],"end":140616106,"feature_type":"variation","strand":1,"source":"dbSNP","start":140616106,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800076745","end":140616108,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140616108,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140616110,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140616110,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1403770627"},{"strand":1,"feature_type":"variation","end":140616116,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616116,"source":"dbSNP","seq_region_name":"7","id":"rs1800076955","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616118,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140616118,"clinical_significance":[],"seq_region_name":"7","id":"rs1366897128"},{"end":140616119,"alleles":["C","CC"],"strand":1,"feature_type":"variation","start":140616119,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1800077151","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1323159635","source":"dbSNP","start":140616122,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140616122,"alleles":["T","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs754456218","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616124,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140616124},{"seq_region_name":"7","id":"rs1354834411","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140616127,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616127,"source":"dbSNP"},{"source":"dbSNP","start":140616128,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140616128,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1800077569"},{"feature_type":"variation","strand":1,"end":140616131,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616131,"clinical_significance":[],"seq_region_name":"7","id":"rs1800077668"},{"clinical_significance":[],"id":"rs1800077749","seq_region_name":"7","feature_type":"variation","strand":1,"end":140616132,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616132},{"feature_type":"variation","strand":1,"end":140616134,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616134,"clinical_significance":[],"id":"rs1800077843","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140616135,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616135,"source":"dbSNP","seq_region_name":"7","id":"rs2130711912","clinical_significance":[]},{"start":140616136,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140616136,"alleles":["G","GGG"],"strand":1,"feature_type":"variation","id":"rs1800077944","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140616139,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140616143,"alleles":["GCCAG","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1800078057"},{"clinical_significance":[],"id":"rs1800078158","seq_region_name":"7","end":140616140,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140616140,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","T"],"end":140616141,"feature_type":"variation","strand":1,"source":"dbSNP","start":140616141,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1800078261"},{"start":140616146,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140616146,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs764748615","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1800078437","seq_region_name":"7","alleles":["T","C"],"end":140616150,"feature_type":"variation","strand":1,"source":"dbSNP","start":140616150,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140616154,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140616154,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1800078545","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1440453158","end":140616157,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140616157,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1585762623","seq_region_name":"7","source":"dbSNP","start":140616162,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140616162,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140616165,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616165,"clinical_significance":[],"seq_region_name":"7","id":"rs1800078852"},{"source":"dbSNP","start":140616169,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140616169,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs150662154"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616170,"source":"dbSNP","strand":1,"feature_type":"variation","end":140616170,"alleles":["C","G"],"seq_region_name":"7","id":"rs1800079097","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140616173,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616173,"clinical_significance":[],"seq_region_name":"7","id":"rs1329205717"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616173,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CC","C"],"end":140616174,"seq_region_name":"7","id":"rs1800079305","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1177393529","end":140616178,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140616178,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616182,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140616182,"clinical_significance":[],"seq_region_name":"7","id":"rs1005108681"},{"id":"rs1800079599","seq_region_name":"7","clinical_significance":[],"start":140616183,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140616183,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1457704161","seq_region_name":"7","source":"dbSNP","start":140616184,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140616184,"alleles":["T","C"],"feature_type":"variation","strand":1},{"alleles":["G","A"],"end":140616188,"feature_type":"variation","strand":1,"source":"dbSNP","start":140616188,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs551708612"},{"id":"rs1800079797","seq_region_name":"7","clinical_significance":[],"start":140616197,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140616197,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs569917454","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616204,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140616204},{"seq_region_name":"7","id":"rs1376128073","clinical_significance":[],"alleles":["A","G"],"end":140616205,"strand":1,"feature_type":"variation","start":140616205,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs901984035","feature_type":"variation","strand":1,"alleles":["A","T"],"end":140616208,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616208},{"alleles":["T","G"],"end":140616219,"feature_type":"variation","strand":1,"source":"dbSNP","start":140616219,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1316479764"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1353669682","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616221,"feature_type":"variation","strand":1,"end":140616221,"alleles":["G","A","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800080488","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140616222,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616222},{"seq_region_name":"7","id":"rs1034636747","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140616228,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616228,"source":"dbSNP"},{"id":"rs1800080704","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616230,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140616230},{"alleles":["G","T"],"end":140616231,"feature_type":"variation","strand":1,"source":"dbSNP","start":140616231,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs777027463"},{"source":"dbSNP","start":140616232,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140616232,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1237941551","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs140148489","feature_type":"variation","strand":1,"end":140616235,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616235},{"clinical_significance":[],"seq_region_name":"7","id":"rs185408085","end":140616236,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140616236,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616238,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140616238,"clinical_significance":[],"seq_region_name":"7","id":"rs1388247943"},{"seq_region_name":"7","id":"rs1200971977","clinical_significance":[],"start":140616239,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140616239,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616240,"feature_type":"variation","strand":1,"end":140616240,"alleles":["G","A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1271342459"},{"alleles":["C","T"],"end":140616241,"strand":1,"feature_type":"variation","start":140616241,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1236853483","seq_region_name":"7","clinical_significance":[]},{"id":"rs1800081646","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616244,"source":"dbSNP","strand":1,"feature_type":"variation","end":140616244,"alleles":["G","A"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616247,"feature_type":"variation","strand":1,"end":140616246,"alleles":["-","GT"],"clinical_significance":[],"seq_region_name":"7","id":"rs1800081756"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616247,"feature_type":"variation","strand":1,"end":140616247,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1800081851"},{"seq_region_name":"7","id":"rs2130712127","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140616248,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616248,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1800081950","clinical_significance":[],"strand":1,"feature_type":"variation","end":140616251,"alleles":["TA","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616250,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616252,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140616252,"id":"rs1800082027","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140616260,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140616260,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1800082126"},{"alleles":["C","G"],"end":140616261,"feature_type":"variation","strand":1,"source":"dbSNP","start":140616261,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1457681391"},{"id":"rs962442251","seq_region_name":"7","clinical_significance":[],"start":140616263,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140616263,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1029157783","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616267,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140616267},{"seq_region_name":"7","id":"rs1156872596","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616268,"source":"dbSNP","strand":1,"feature_type":"variation","end":140616268,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs567333474","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616276,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140616276},{"clinical_significance":[],"seq_region_name":"7","id":"rs1439623562","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616288,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140616288},{"start":140616292,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140616292,"alleles":["G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1800082831","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585762864","clinical_significance":[],"end":140616293,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140616293,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140616294,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616294,"clinical_significance":[],"seq_region_name":"7","id":"rs1011772399"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616298,"source":"dbSNP","strand":1,"feature_type":"variation","end":140616298,"alleles":["G","A"],"seq_region_name":"7","id":"rs1021274080","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585762906","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616299,"feature_type":"variation","strand":1,"end":140616299,"alleles":["T","G"]},{"feature_type":"variation","strand":1,"end":140616300,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616300,"clinical_significance":[],"id":"rs967466771","seq_region_name":"7"},{"source":"dbSNP","start":140616305,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140616305,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1201488254"},{"feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140616310,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616310,"clinical_significance":[],"seq_region_name":"7","id":"rs977337218"},{"clinical_significance":[],"seq_region_name":"7","id":"rs9691747","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616311,"feature_type":"variation","strand":1,"end":140616311,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1267070033","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616316,"feature_type":"variation","strand":1,"end":140616316,"alleles":["C","T"]},{"start":140616318,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140616318,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1221364279","clinical_significance":[]},{"alleles":["C","A","T"],"end":140616320,"feature_type":"variation","strand":1,"source":"dbSNP","start":140616320,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1025258901"},{"seq_region_name":"7","id":"rs1213775349","clinical_significance":[],"strand":1,"feature_type":"variation","end":140616324,"alleles":["T","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616324,"source":"dbSNP"},{"end":140616325,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140616325,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1800084233","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140616326,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616326,"clinical_significance":[],"seq_region_name":"7","id":"rs1471855283"},{"clinical_significance":[],"id":"rs111424767","seq_region_name":"7","source":"dbSNP","start":140616327,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140616327,"alleles":["A","C"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616328,"source":"dbSNP","strand":1,"feature_type":"variation","end":140616328,"alleles":["C","T"],"id":"rs1800084573","seq_region_name":"7","clinical_significance":[]},{"start":140616332,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140616332,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1800084651","clinical_significance":[]},{"source":"dbSNP","start":140616334,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140616334,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs546353600"},{"seq_region_name":"7","id":"rs762199149","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140616335,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616335,"source":"dbSNP"},{"end":140616336,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140616336,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs987107616","seq_region_name":"7"},{"start":140616340,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140616340,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1329092054","clinical_significance":[]},{"seq_region_name":"7","id":"rs991313269","clinical_significance":[],"start":140616341,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140616341,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616344,"source":"dbSNP","strand":1,"feature_type":"variation","end":140616344,"alleles":["A","G"],"id":"rs577978374","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1800085357","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616347,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140616347},{"clinical_significance":[],"seq_region_name":"7","id":"rs1342530313","feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140616348,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616348},{"clinical_significance":[],"seq_region_name":"7","id":"rs915776228","source":"dbSNP","start":140616349,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140616349,"alleles":["G","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1800085681","clinical_significance":[],"start":140616351,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140616351,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"start":140616352,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140616352,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1800085795","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140616356,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616356,"source":"dbSNP","seq_region_name":"7","id":"rs1296452541","clinical_significance":[]},{"id":"rs911152929","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140616357,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616357,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1174868033","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616359,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140616359},{"strand":1,"feature_type":"variation","end":140616360,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616360,"source":"dbSNP","seq_region_name":"7","id":"rs1800086250","clinical_significance":[]},{"end":140616370,"alleles":["ACACACA","ACACA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140616364,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1377478145"},{"source":"dbSNP","start":140616365,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140616365,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1194769253"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1438895266","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616369,"feature_type":"variation","strand":1,"end":140616369,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs948141183","source":"dbSNP","start":140616371,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140616371,"alleles":["A","C","G"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140616376,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140616376,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1800086798","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140616380,"alleles":["T","C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616380,"clinical_significance":[],"seq_region_name":"7","id":"rs539476520"},{"clinical_significance":[],"id":"rs909184284","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140616387,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616387},{"clinical_significance":[],"seq_region_name":"7","id":"rs1445958173","source":"dbSNP","start":140616392,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140616392,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1800087228","clinical_significance":[],"strand":1,"feature_type":"variation","end":140616393,"alleles":["A","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616393,"source":"dbSNP"},{"alleles":["G","A"],"end":140616400,"feature_type":"variation","strand":1,"source":"dbSNP","start":140616400,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1585763172","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs62485842","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616401,"feature_type":"variation","strand":1,"end":140616401,"alleles":["A","T"]},{"source":"dbSNP","start":140616401,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140616403,"alleles":["AAA","AAAA"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1278712093","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140616403,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616403,"source":"dbSNP","seq_region_name":"7","id":"rs1800087615","clinical_significance":[]},{"source":"dbSNP","start":140616405,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140616405,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs914426623"},{"clinical_significance":[],"id":"rs1800087834","seq_region_name":"7","source":"dbSNP","start":140616406,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140616406,"alleles":["A","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130712410","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140616407,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616407},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616410,"source":"dbSNP","strand":1,"feature_type":"variation","end":140616410,"alleles":["T","A"],"seq_region_name":"7","id":"rs1338122800","clinical_significance":[]},{"seq_region_name":"7","id":"rs1036535054","clinical_significance":[],"end":140616413,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","start":140616413,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs946113283","clinical_significance":[],"start":140616415,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140616415,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1800088286","clinical_significance":[],"end":140616418,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140616418,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1341087383","seq_region_name":"7","end":140616422,"alleles":["G","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140616422,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140616424,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140616424,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1800088392","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616428,"feature_type":"variation","strand":1,"end":140616428,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1800088492"},{"seq_region_name":"7","id":"rs1800088598","clinical_significance":[],"end":140616431,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140616431,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140616434,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140616434,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1041848529"},{"alleles":["G","T"],"end":140616435,"feature_type":"variation","strand":1,"source":"dbSNP","start":140616435,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1800088805"},{"source":"dbSNP","start":140616436,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140616436,"alleles":["C","A","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs10952779"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616436,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","-"],"end":140616436,"seq_region_name":"7","id":"rs1341211965","clinical_significance":[]},{"seq_region_name":"7","id":"rs182263915","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616437,"source":"dbSNP","strand":1,"feature_type":"variation","end":140616437,"alleles":["G","A","T"]},{"feature_type":"variation","strand":1,"end":140616440,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616440,"clinical_significance":[],"seq_region_name":"7","id":"rs1421898644"},{"feature_type":"variation","strand":1,"end":140616441,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616441,"clinical_significance":[],"id":"rs1585763324","seq_region_name":"7"},{"id":"rs1585763345","seq_region_name":"7","clinical_significance":[],"alleles":["T","G"],"end":140616444,"strand":1,"feature_type":"variation","start":140616444,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140616450,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140616450,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1056428456","clinical_significance":[]},{"id":"rs1585763361","seq_region_name":"7","clinical_significance":[],"alleles":["T","G"],"end":140616451,"strand":1,"feature_type":"variation","start":140616451,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616455,"feature_type":"variation","strand":1,"alleles":["T","-"],"end":140616455,"clinical_significance":[],"seq_region_name":"7","id":"rs894728182"},{"id":"rs1237560279","seq_region_name":"7","clinical_significance":[],"end":140616455,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140616455,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140616456,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616456,"source":"dbSNP","seq_region_name":"7","id":"rs1800089737","clinical_significance":[]},{"start":140616457,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140616457,"alleles":["C","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1800089849","clinical_significance":[]},{"seq_region_name":"7","id":"rs1188938389","clinical_significance":[],"alleles":["T","A"],"end":140616458,"strand":1,"feature_type":"variation","start":140616458,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140616461,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616461,"source":"dbSNP","seq_region_name":"7","id":"rs1800090047","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140616462,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616462,"source":"dbSNP","id":"rs1800090175","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs972896072","clinical_significance":[],"strand":1,"feature_type":"variation","end":140616476,"alleles":["GGTATGGATTTTGG","GG"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616463,"source":"dbSNP"},{"end":140616464,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140616464,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130712569"},{"start":140616465,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C","G"],"end":140616465,"strand":1,"feature_type":"variation","id":"rs1585763402","seq_region_name":"7","clinical_significance":[]},{"start":140616466,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140616466,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1800090480","clinical_significance":[]},{"alleles":["A","AA"],"end":140616470,"feature_type":"variation","strand":1,"source":"dbSNP","start":140616470,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1664550491"},{"seq_region_name":"7","id":"rs1800090586","clinical_significance":[],"start":140616474,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140616474,"alleles":["T","A","G"],"strand":1,"feature_type":"variation"},{"id":"rs540683011","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616475,"source":"dbSNP","strand":1,"feature_type":"variation","end":140616479,"alleles":["GGGGG","GGGG"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1440762456","feature_type":"variation","strand":1,"end":140616488,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616488},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800090961","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140616490,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616490},{"clinical_significance":[],"id":"rs1800091052","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616496,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140616496},{"id":"rs1800091152","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140616506,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616506,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1800091310","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140616512,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616512},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800091449","source":"dbSNP","start":140616514,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140616514,"alleles":["G","C"],"feature_type":"variation","strand":1},{"alleles":["G","A","T"],"end":140616516,"feature_type":"variation","strand":1,"source":"dbSNP","start":140616516,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1319786281"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1016424458","source":"dbSNP","start":140616517,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140616522,"alleles":["GTTGTT","GTT"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1585763446","clinical_significance":[],"alleles":["T","G"],"end":140616518,"strand":1,"feature_type":"variation","start":140616518,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563180431","end":140616524,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140616524,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616526,"source":"dbSNP","strand":1,"feature_type":"variation","end":140616526,"alleles":["C","T"],"seq_region_name":"7","id":"rs1050543035","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800092492","source":"dbSNP","start":140616527,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140616527,"feature_type":"variation","strand":1},{"end":140616529,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140616529,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs898034882"},{"source":"dbSNP","start":140616531,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140616531,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs993859760"},{"seq_region_name":"7","id":"rs1800092953","clinical_significance":[],"end":140616533,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140616533,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1800093067","seq_region_name":"7","source":"dbSNP","start":140616537,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140616537,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1800093171","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140616538,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616538,"source":"dbSNP"},{"alleles":["T","C"],"end":140616540,"strand":1,"feature_type":"variation","start":140616540,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1800093273","clinical_significance":[]},{"seq_region_name":"7","id":"rs1800093381","clinical_significance":[],"alleles":["A","C"],"end":140616544,"strand":1,"feature_type":"variation","start":140616544,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140616546,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140616546,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1800093481","clinical_significance":[]},{"seq_region_name":"7","id":"rs1800093575","clinical_significance":[],"strand":1,"feature_type":"variation","end":140616550,"alleles":["CC","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616549,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140616551,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616551,"clinical_significance":[],"seq_region_name":"7","id":"rs1800093693"},{"start":140616552,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140616552,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1242634815","clinical_significance":[]},{"seq_region_name":"7","id":"rs1242881750","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140616554,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616554,"source":"dbSNP"},{"id":"rs1563180442","seq_region_name":"7","clinical_significance":[],"start":140616558,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140616558,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616559,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140616559,"id":"rs1382096010","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585763498","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616562,"feature_type":"variation","strand":1,"end":140616562,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1025376108","feature_type":"variation","strand":1,"end":140616564,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616564},{"end":140616565,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140616565,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1478901071"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616569,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140616569,"clinical_significance":[],"seq_region_name":"7","id":"rs889307040"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800094633","alleles":["G","T"],"end":140616586,"feature_type":"variation","strand":1,"source":"dbSNP","start":140616586,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1585763523","seq_region_name":"7","clinical_significance":[],"start":140616587,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140616587,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616589,"source":"dbSNP","strand":1,"feature_type":"variation","end":140616589,"alleles":["A","T"],"seq_region_name":"7","id":"rs2130712741","clinical_significance":[]},{"id":"rs1793919263","seq_region_name":"7","clinical_significance":[],"start":140616602,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140616602,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140616608,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616608,"source":"dbSNP","seq_region_name":"7","id":"rs1800094825","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1011301342","source":"dbSNP","start":140616611,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140616611,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616612,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140616612,"seq_region_name":"7","id":"rs1585763540","clinical_significance":[]},{"seq_region_name":"7","id":"rs575815312","clinical_significance":[],"end":140616613,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140616613,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616614,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140616614,"clinical_significance":[],"seq_region_name":"7","id":"rs1800095213"},{"end":140616619,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140616619,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1800095319"},{"seq_region_name":"7","id":"rs967037280","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616620,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140616620},{"seq_region_name":"7","id":"rs1563180465","clinical_significance":[],"end":140616627,"alleles":["AAAAAAAA","AAAAAAA"],"strand":1,"feature_type":"variation","start":140616620,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1422580441","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140616632,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616632},{"clinical_significance":[],"seq_region_name":"7","id":"rs186440509","source":"dbSNP","start":140616633,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140616633,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1035389135","source":"dbSNP","start":140616634,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140616634,"alleles":["G","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1585763586","clinical_significance":[],"alleles":["A","G"],"end":140616640,"strand":1,"feature_type":"variation","start":140616640,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140616655,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616655,"source":"dbSNP","seq_region_name":"7","id":"rs1800095904","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616657,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140616657,"clinical_significance":[],"seq_region_name":"7","id":"rs1800096000"},{"end":140616658,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140616658,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1800096102","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130712821","source":"dbSNP","start":140616660,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140616660,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs188264954","clinical_significance":[],"end":140616662,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140616662,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800096300","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616665,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140616665},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585763605","source":"dbSNP","start":140616674,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140616674,"alleles":["C","T"],"feature_type":"variation","strand":1},{"end":140616677,"alleles":["G","C","T"],"strand":1,"feature_type":"variation","start":140616677,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs990512283","clinical_significance":[]},{"start":140616686,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140616686,"alleles":["A","T"],"strand":1,"feature_type":"variation","id":"rs1800096608","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1384046332","source":"dbSNP","start":140616693,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140616693,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs2130712858","clinical_significance":[],"end":140616695,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140616695,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1585763632","seq_region_name":"7","clinical_significance":[],"start":140616701,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140616701,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"id":"rs1800096919","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616707,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140616707},{"end":140616714,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140616714,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1800097062","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800097186","source":"dbSNP","start":140616724,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140616724,"alleles":["G","A","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800097301","feature_type":"variation","strand":1,"end":140616732,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616732},{"end":140616735,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140616735,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs914389626","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs781089515","source":"dbSNP","start":140616735,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AAA","A"],"end":140616737,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800097605","alleles":["G","C"],"end":140616738,"feature_type":"variation","strand":1,"source":"dbSNP","start":140616738,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1236150682","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616739,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140616739},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800097791","feature_type":"variation","strand":1,"end":140616744,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616744},{"clinical_significance":[],"seq_region_name":"7","id":"rs1174242839","source":"dbSNP","start":140616748,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140616748,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs2130712905","clinical_significance":[],"alleles":["CATAGT","-"],"end":140616754,"strand":1,"feature_type":"variation","start":140616749,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140616751,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616751,"clinical_significance":[],"seq_region_name":"7","id":"rs1452439980"},{"seq_region_name":"7","id":"rs1400052926","clinical_significance":[],"start":140616761,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140616761,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800098326","feature_type":"variation","strand":1,"end":140616763,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616763},{"source":"dbSNP","start":140616769,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140616769,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1292350599"},{"feature_type":"variation","strand":1,"end":140616770,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616770,"clinical_significance":[],"seq_region_name":"7","id":"rs959932751"},{"start":140616771,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140616771,"strand":1,"feature_type":"variation","id":"rs1800098617","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616774,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140616774,"clinical_significance":[],"id":"rs1800098706","seq_region_name":"7"},{"source":"dbSNP","start":140616775,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140616775,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1318361672"},{"seq_region_name":"7","id":"rs1800098952","clinical_significance":[],"start":140616777,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140616777,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs991427894","clinical_significance":[],"strand":1,"feature_type":"variation","end":140616779,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616779,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616792,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140616792,"seq_region_name":"7","id":"rs181013354","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs952663833","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140616794,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616794},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800099307","source":"dbSNP","start":140616800,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A","C"],"end":140616800,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800099477","source":"dbSNP","start":140616801,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140616801,"alleles":["G","A","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs185636264","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140616808,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616808},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140616811,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616811,"source":"dbSNP","seq_region_name":"7","id":"rs532958266","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800099764","feature_type":"variation","strand":1,"end":140616815,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616815},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616818,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140616818,"clinical_significance":[],"id":"rs1242964749","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140616824,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616824,"clinical_significance":[],"seq_region_name":"7","id":"rs938641484"},{"clinical_significance":[],"id":"rs1585763780","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616826,"feature_type":"variation","strand":1,"end":140616826,"alleles":["A","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800100151","source":"dbSNP","start":140616827,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140616827,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1340296068","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616837,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140616837},{"start":140616842,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140616842,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1800100339","clinical_significance":[]},{"seq_region_name":"7","id":"rs1800100437","clinical_significance":[],"strand":1,"feature_type":"variation","end":140616843,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616843,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140616844,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616844,"source":"dbSNP","id":"rs1437578237","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616845,"source":"dbSNP","strand":1,"feature_type":"variation","end":140616845,"alleles":["C","T"],"seq_region_name":"7","id":"rs1800100593","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140616849,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616849,"source":"dbSNP","seq_region_name":"7","id":"rs1800100690","clinical_significance":[]},{"end":140616860,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140616860,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1351966148"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616868,"source":"dbSNP","strand":1,"feature_type":"variation","end":140616868,"alleles":["A","C","T"],"seq_region_name":"7","id":"rs1325165788","clinical_significance":[]},{"start":140616869,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TTTTTTT","TTTTTT"],"end":140616875,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1563180537","clinical_significance":[]},{"id":"rs909289877","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140616871,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616871,"source":"dbSNP"},{"source":"dbSNP","start":140616874,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140616874,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1224575453","seq_region_name":"7"},{"source":"dbSNP","start":140616883,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C","T"],"end":140616883,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1441472549"},{"end":140616884,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140616884,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs940826164","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616885,"source":"dbSNP","strand":1,"feature_type":"variation","end":140616885,"alleles":["T","C"],"id":"rs972033091","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","C"],"end":140616891,"strand":1,"feature_type":"variation","start":140616891,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1478256349","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585763901","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616897,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140616897},{"clinical_significance":[],"seq_region_name":"7","id":"rs146863682","alleles":["C","A"],"end":140616899,"feature_type":"variation","strand":1,"source":"dbSNP","start":140616899,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140616902,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140616902,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs894499419","clinical_significance":[]},{"start":140616904,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140616904,"strand":1,"feature_type":"variation","id":"rs60903892","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140616909,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140616909,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1800102059"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1286827238","end":140616910,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140616910,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616915,"feature_type":"variation","strand":1,"end":140616915,"alleles":["T","G"],"clinical_significance":[],"id":"rs1218829411","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616916,"source":"dbSNP","strand":1,"feature_type":"variation","end":140616916,"alleles":["G","C"],"seq_region_name":"7","id":"rs1800102360","clinical_significance":[]},{"id":"rs1563180569","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616926,"source":"dbSNP","strand":1,"feature_type":"variation","end":140616925,"alleles":["-","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563180575","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616926,"feature_type":"variation","strand":1,"end":140616926,"alleles":["C","A","T"]},{"seq_region_name":"7","id":"rs1800102652","clinical_significance":[],"strand":1,"feature_type":"variation","end":140616929,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616929,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1352173415","clinical_significance":[],"end":140616934,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140616934,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616935,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140616935,"id":"rs2130713174","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","T"],"end":140616939,"feature_type":"variation","strand":1,"source":"dbSNP","start":140616939,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1800102843"},{"id":"rs1284242888","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616940,"source":"dbSNP","strand":1,"feature_type":"variation","end":140616940,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs751676701","end":140616941,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140616941,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140616943,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616943,"source":"dbSNP","id":"rs1224308493","seq_region_name":"7","clinical_significance":[]},{"start":140616944,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140616944,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs1800103404","seq_region_name":"7","clinical_significance":[]},{"end":140616950,"alleles":["CCC","CC"],"strand":1,"feature_type":"variation","start":140616948,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1038382733","clinical_significance":[]},{"clinical_significance":[],"id":"rs756019093","seq_region_name":"7","alleles":["C","T"],"end":140616950,"feature_type":"variation","strand":1,"source":"dbSNP","start":140616950,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616951,"feature_type":"variation","strand":1,"end":140616951,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs530860933"},{"source":"dbSNP","start":140616952,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140616952,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1563180601"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800103927","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140616957,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616957},{"strand":1,"feature_type":"variation","end":140616960,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616960,"source":"dbSNP","seq_region_name":"7","id":"rs1402735243","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616961,"feature_type":"variation","strand":1,"end":140616961,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs777712521"},{"end":140616963,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140616963,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1420934464","clinical_significance":[]},{"alleles":["T","C"],"end":140616967,"feature_type":"variation","strand":1,"source":"dbSNP","start":140616967,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130713230"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616972,"feature_type":"variation","strand":1,"end":140616972,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1800104360"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616983,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140616983,"clinical_significance":[],"id":"rs993639025","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1158380834","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140616989,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616989},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140616990,"feature_type":"variation","strand":1,"end":140616990,"alleles":["T","C"],"clinical_significance":[],"id":"rs1414956598","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140616991,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616991,"source":"dbSNP","seq_region_name":"7","id":"rs1800104763","clinical_significance":[]},{"seq_region_name":"7","id":"rs1427022347","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140616993,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140616993,"source":"dbSNP"},{"end":140616998,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140616998,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1196932895","clinical_significance":[]},{"id":"rs1800105060","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140616999,"strand":1,"feature_type":"variation","start":140616999,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140617000,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617000,"source":"dbSNP","id":"rs1046774997","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140617002,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617002,"clinical_significance":[],"seq_region_name":"7","id":"rs143153206"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140617003,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617003,"clinical_significance":[],"id":"rs746756177","seq_region_name":"7"},{"seq_region_name":"7","id":"rs2130713289","clinical_significance":[],"alleles":["T","C"],"end":140617006,"strand":1,"feature_type":"variation","start":140617006,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140617008,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617008,"source":"dbSNP","seq_region_name":"7","id":"rs1487374189","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130713303","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140617012,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617012},{"end":140617014,"alleles":["C","A","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140617014,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs116616871"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1314398156","source":"dbSNP","start":140617015,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140617015,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140617016,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140617016,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs964072958"},{"strand":1,"feature_type":"variation","end":140617019,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617019,"source":"dbSNP","seq_region_name":"7","id":"rs2130713331","clinical_significance":[]},{"end":140617020,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140617020,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1223240175","clinical_significance":[]},{"source":"dbSNP","start":140617021,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140617021,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1322428433"},{"seq_region_name":"7","id":"rs998633423","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140617024,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617024,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130713348","alleles":["A","T"],"end":140617025,"feature_type":"variation","strand":1,"source":"dbSNP","start":140617025,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1480633127","clinical_significance":[],"strand":1,"feature_type":"variation","end":140617034,"alleles":["GTAGT","GT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617030,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1401457839","clinical_significance":[],"alleles":["A","G"],"end":140617032,"strand":1,"feature_type":"variation","start":140617032,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617033,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140617033,"seq_region_name":"7","id":"rs1359324774","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs770886747","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140617047,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617047},{"clinical_significance":[],"seq_region_name":"7","id":"rs1021567301","end":140617050,"alleles":["GGGG","GGGGG"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140617047,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1800106715","clinical_significance":[],"alleles":["G","A"],"end":140617048,"strand":1,"feature_type":"variation","start":140617048,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1448673689","feature_type":"variation","strand":1,"end":140617050,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617050},{"source":"dbSNP","start":140617058,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140617058,"alleles":["A","AA"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1800106927"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617060,"feature_type":"variation","strand":1,"end":140617060,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs528232114"},{"alleles":["G","A"],"end":140617064,"feature_type":"variation","strand":1,"source":"dbSNP","start":140617064,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1174017306"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800107235","end":140617069,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140617069,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140617072,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140617072,"strand":1,"feature_type":"variation","id":"rs547074759","seq_region_name":"7","clinical_significance":[]},{"end":140617073,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140617073,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1424040368","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1200794906","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140617077,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617077},{"seq_region_name":"7","id":"rs1375752662","clinical_significance":[],"start":140617078,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140617078,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs967183027","feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140617083,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617083},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800107946","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617084,"feature_type":"variation","strand":1,"end":140617084,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs895500163","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617085,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140617085},{"clinical_significance":[],"id":"rs145484125","seq_region_name":"7","end":140617086,"alleles":["G","A","C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140617086,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140617090,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617090,"clinical_significance":[],"id":"rs1458545368","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1260381660","feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140617092,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617092},{"source":"dbSNP","start":140617094,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140617094,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1800108709"},{"seq_region_name":"7","id":"rs1800108803","clinical_significance":[],"start":140617101,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140617101,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1159089972","alleles":["C","T"],"end":140617104,"feature_type":"variation","strand":1,"source":"dbSNP","start":140617104,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140617105,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140617105,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs538666825"},{"source":"dbSNP","start":140617109,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140617109,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1800109112"},{"feature_type":"variation","strand":1,"end":140617110,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617110,"clinical_significance":[],"seq_region_name":"7","id":"rs1800109216"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800109312","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617118,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140617118},{"seq_region_name":"7","id":"rs952536900","clinical_significance":[],"strand":1,"feature_type":"variation","end":140617119,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617119,"source":"dbSNP"},{"start":140617120,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140617120,"alleles":["A","G"],"strand":1,"feature_type":"variation","id":"rs1800109495","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","A","G"],"end":140617124,"strand":1,"feature_type":"variation","start":140617124,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1800109593","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1660054841","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617130,"feature_type":"variation","strand":1,"end":140617130,"alleles":["T","C"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617131,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140617131,"seq_region_name":"7","id":"rs1417401619","clinical_significance":[]},{"seq_region_name":"7","id":"rs1294265891","clinical_significance":[],"start":140617133,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140617133,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1228342497","clinical_significance":[],"start":140617137,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140617137,"strand":1,"feature_type":"variation"},{"id":"rs148844683","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617140,"source":"dbSNP","strand":1,"feature_type":"variation","end":140617140,"alleles":["G","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617147,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140617147,"clinical_significance":[],"seq_region_name":"7","id":"rs143515218"},{"clinical_significance":[],"seq_region_name":"7","id":"rs745532968","source":"dbSNP","start":140617148,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140617148,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs972149146","source":"dbSNP","start":140617156,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140617156,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1303805429","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617157,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140617157},{"source":"dbSNP","start":140617158,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140617158,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1329730588"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1460665475","alleles":["G","A","T"],"end":140617159,"feature_type":"variation","strand":1,"source":"dbSNP","start":140617159,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140617164,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140617164,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1372682356"},{"seq_region_name":"7","id":"rs1165600316","clinical_significance":[],"alleles":["G","C"],"end":140617167,"strand":1,"feature_type":"variation","start":140617167,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140617168,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140617168,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs150961450","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617170,"feature_type":"variation","strand":1,"end":140617170,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1800111165"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617172,"feature_type":"variation","strand":1,"end":140617172,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1383455577"},{"clinical_significance":[],"seq_region_name":"7","id":"rs537441807","feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140617173,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617173},{"seq_region_name":"7","id":"rs1037887953","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617180,"source":"dbSNP","strand":1,"feature_type":"variation","end":140617180,"alleles":["G","T"]},{"seq_region_name":"7","id":"rs1194392973","clinical_significance":[],"alleles":["T","G"],"end":140617181,"strand":1,"feature_type":"variation","start":140617181,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617184,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140617184,"clinical_significance":[],"seq_region_name":"7","id":"rs1479465642"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617185,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140617185,"seq_region_name":"7","id":"rs1800111770","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1233085434","feature_type":"variation","strand":1,"end":140617186,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617186},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617187,"source":"dbSNP","strand":1,"feature_type":"variation","end":140617187,"alleles":["C","T"],"seq_region_name":"7","id":"rs191529535","clinical_significance":[]},{"clinical_significance":[],"id":"rs1250457363","seq_region_name":"7","source":"dbSNP","start":140617190,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140617190,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800112161","alleles":["T","C"],"end":140617191,"feature_type":"variation","strand":1,"source":"dbSNP","start":140617191,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140617192,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140617192,"strand":1,"feature_type":"variation","id":"rs1221803462","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140617194,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140617194,"alleles":["T","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1323073847"},{"clinical_significance":[],"seq_region_name":"7","id":"rs919527032","source":"dbSNP","start":140617199,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140617199,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1280652339","feature_type":"variation","strand":1,"end":140617202,"alleles":["A","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617202},{"alleles":["C","G"],"end":140617204,"feature_type":"variation","strand":1,"source":"dbSNP","start":140617204,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs113868713"},{"start":140617205,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140617205,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1800112776","clinical_significance":[]},{"start":140617207,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140617207,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1800112886","clinical_significance":[]},{"clinical_significance":[],"id":"rs771894408","seq_region_name":"7","alleles":["C","T"],"end":140617213,"feature_type":"variation","strand":1,"source":"dbSNP","start":140617213,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1355941200","clinical_significance":[],"end":140617216,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140617216,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800113227","source":"dbSNP","start":140617217,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140617217,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs183090111","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140617218,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617218,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140617219,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617219,"source":"dbSNP","id":"rs2130713640","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1800113588","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617222,"source":"dbSNP","strand":1,"feature_type":"variation","end":140617222,"alleles":["G","A","T"]},{"seq_region_name":"7","id":"rs1389413687","clinical_significance":[],"end":140617227,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140617227,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["C","G"],"end":140617229,"feature_type":"variation","strand":1,"source":"dbSNP","start":140617229,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs933337217"},{"end":140617231,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140617231,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1800114845","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1294382575","clinical_significance":[],"alleles":["C","A"],"end":140617232,"strand":1,"feature_type":"variation","start":140617232,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1459628198","clinical_significance":[],"alleles":["C","T"],"end":140617234,"strand":1,"feature_type":"variation","start":140617234,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1585764642","seq_region_name":"7","source":"dbSNP","start":140617238,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140617238,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1800115272","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617240,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140617240},{"start":140617241,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140617241,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","id":"rs986313605","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140617242,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617242,"source":"dbSNP","seq_region_name":"7","id":"rs1051873133","clinical_significance":[]},{"end":140617243,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140617243,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130713693","clinical_significance":[]},{"source":"dbSNP","start":140617246,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140617246,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1382647192"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140617248,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617248,"source":"dbSNP","seq_region_name":"7","id":"rs890659177","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140617249,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617249,"source":"dbSNP","seq_region_name":"7","id":"rs1268485044","clinical_significance":[]},{"alleles":["TTTT","TTT"],"end":140617252,"feature_type":"variation","strand":1,"source":"dbSNP","start":140617249,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1418897393"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140617260,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617260,"clinical_significance":[],"seq_region_name":"7","id":"rs540422954"},{"id":"rs1800116170","seq_region_name":"7","clinical_significance":[],"end":140617261,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140617261,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1800116276","clinical_significance":[],"end":140617266,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140617266,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1007960364","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140617268,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617268,"source":"dbSNP"},{"start":140617270,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140617270,"alleles":["G","-"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1800116481","clinical_significance":[]},{"source":"dbSNP","start":140617277,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140617277,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1490722803"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1490563702","source":"dbSNP","start":140617280,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140617280,"feature_type":"variation","strand":1},{"start":140617287,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140617287,"strand":1,"feature_type":"variation","id":"rs1800116784","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1039887585","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617294,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140617294},{"clinical_significance":[],"seq_region_name":"7","id":"rs1221039866","end":140617298,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140617298,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs367775421","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617304,"source":"dbSNP","strand":1,"feature_type":"variation","end":140617304,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs553052976","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617307,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140617307},{"source":"dbSNP","start":140617308,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140617308,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1800117314"},{"seq_region_name":"7","id":"rs577777719","clinical_significance":[],"strand":1,"feature_type":"variation","end":140617311,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617311,"source":"dbSNP"},{"start":140617314,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140617314,"alleles":["T","G"],"strand":1,"feature_type":"variation","id":"rs1236755987","seq_region_name":"7","clinical_significance":[]},{"end":140617315,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140617315,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1800117673"},{"feature_type":"variation","strand":1,"end":140617316,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617316,"clinical_significance":[],"seq_region_name":"7","id":"rs1800117782"},{"clinical_significance":[],"id":"rs545108394","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617317,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140617317},{"source":"dbSNP","start":140617320,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140617320,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs7776899"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800118189","end":140617324,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140617324,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140617327,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617327,"clinical_significance":[],"seq_region_name":"7","id":"rs1800118305"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617328,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140617328,"seq_region_name":"7","id":"rs186834694","clinical_significance":[]},{"clinical_significance":[],"id":"rs1432391846","seq_region_name":"7","source":"dbSNP","start":140617329,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140617329,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140617330,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617330,"clinical_significance":[],"id":"rs1800118517","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140617332,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617332,"clinical_significance":[],"seq_region_name":"7","id":"rs1343829455"},{"strand":1,"feature_type":"variation","end":140617333,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617333,"source":"dbSNP","seq_region_name":"7","id":"rs142141519","clinical_significance":[]},{"alleles":["G","A"],"end":140617344,"strand":1,"feature_type":"variation","start":140617344,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs7787030","clinical_significance":[]},{"clinical_significance":[],"id":"rs1800119014","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617346,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140617346},{"start":140617348,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140617348,"alleles":["C","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs777130864","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1157402163","source":"dbSNP","start":140617356,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140617356,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1453661198","seq_region_name":"7","source":"dbSNP","start":140617357,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140617357,"alleles":["C","A","T"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140617359,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617359,"clinical_significance":[],"seq_region_name":"7","id":"rs1378591301"},{"seq_region_name":"7","id":"rs1800119843","clinical_significance":[],"strand":1,"feature_type":"variation","end":140617360,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617360,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1437258043","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140617364,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617364,"source":"dbSNP"},{"source":"dbSNP","start":140617365,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140617365,"alleles":["T","A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs533657671"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617367,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140617367,"seq_region_name":"7","id":"rs1481233533","clinical_significance":[]},{"seq_region_name":"7","id":"rs765619614","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140617368,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617368,"source":"dbSNP"},{"source":"dbSNP","start":140617369,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140617369,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs960166341"},{"start":140617370,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140617370,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs528312388","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617371,"feature_type":"variation","strand":1,"end":140617371,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs2130713888"},{"seq_region_name":"7","id":"rs1263216446","clinical_significance":[],"end":140617374,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140617374,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617382,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140617382,"seq_region_name":"7","id":"rs1012589787","clinical_significance":[]},{"id":"rs1800121534","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617386,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140617386},{"feature_type":"variation","strand":1,"end":140617387,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617387,"clinical_significance":[],"seq_region_name":"7","id":"rs991575713"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130713926","end":140617389,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140617389,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs915993594","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617392,"feature_type":"variation","strand":1,"end":140617392,"alleles":["T","G"]},{"seq_region_name":"7","id":"rs1800122047","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617403,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["ACTCA","A"],"end":140617407},{"source":"dbSNP","start":140617409,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140617409,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1386628886"},{"end":140617410,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140617410,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1256398428","clinical_significance":[]},{"seq_region_name":"7","id":"rs963386251","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617412,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140617412},{"start":140617413,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140617413,"alleles":["T","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1800122600","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800122697","source":"dbSNP","start":140617415,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140617415,"feature_type":"variation","strand":1},{"alleles":["A","G"],"end":140617417,"feature_type":"variation","strand":1,"source":"dbSNP","start":140617417,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs145966269"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800122923","end":140617418,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140617418,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617420,"feature_type":"variation","strand":1,"end":140617420,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1321119728"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617422,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140617422,"clinical_significance":[],"id":"rs1800123126","seq_region_name":"7"},{"source":"dbSNP","start":140617425,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140617432,"alleles":["TTTCTTTT","TTT"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1332614120"},{"clinical_significance":[],"id":"rs1022667944","seq_region_name":"7","source":"dbSNP","start":140617428,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140617428,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1800123491","seq_region_name":"7","alleles":["T","C"],"end":140617430,"feature_type":"variation","strand":1,"source":"dbSNP","start":140617430,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617435,"feature_type":"variation","strand":1,"end":140617435,"alleles":["C","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs117908060"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800123767","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617446,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140617446},{"seq_region_name":"7","id":"rs532499993","clinical_significance":[],"end":140617449,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140617449,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800123965","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617452,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140617452},{"seq_region_name":"7","id":"rs1005498216","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140617458,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617458,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140617462,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617462,"source":"dbSNP","seq_region_name":"7","id":"rs1316244769","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140617467,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617467,"source":"dbSNP","seq_region_name":"7","id":"rs763129625","clinical_significance":[]},{"seq_region_name":"7","id":"rs1800124355","clinical_significance":[],"end":140617473,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140617473,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140617475,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140617475,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1800124458","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1403489376","end":140617477,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140617477,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs919294966","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617483,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140617483},{"seq_region_name":"7","id":"rs1468616354","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617485,"source":"dbSNP","strand":1,"feature_type":"variation","end":140617485,"alleles":["G","T"]},{"start":140617487,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140617487,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs550660967","clinical_significance":[]},{"seq_region_name":"7","id":"rs568949227","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617490,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140617490},{"clinical_significance":[],"seq_region_name":"7","id":"rs564067066","feature_type":"variation","strand":1,"end":140617491,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617491},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140617493,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617493,"clinical_significance":[],"seq_region_name":"7","id":"rs1477910055"},{"id":"rs972093771","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617495,"source":"dbSNP","strand":1,"feature_type":"variation","end":140617495,"alleles":["C","A","T"]},{"feature_type":"variation","strand":1,"end":140617496,"alleles":["G","A","C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617496,"clinical_significance":[],"seq_region_name":"7","id":"rs1051991034"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617498,"feature_type":"variation","strand":1,"end":140617498,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1263971266"},{"alleles":["T","G"],"end":140617499,"feature_type":"variation","strand":1,"source":"dbSNP","start":140617499,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs968812330"},{"strand":1,"feature_type":"variation","end":140617500,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617500,"source":"dbSNP","seq_region_name":"7","id":"rs1800125889","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585765219","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140617502,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617502,"source":"dbSNP"},{"start":140617503,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140617503,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1030381549","clinical_significance":[]},{"source":"dbSNP","start":140617505,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140617505,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1488029889","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617506,"feature_type":"variation","strand":1,"end":140617506,"alleles":["C","CGAGGTC"],"clinical_significance":[],"id":"rs1205448053","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1262259574","feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140617507,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617507},{"start":140617508,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140617508,"strand":1,"feature_type":"variation","id":"rs1456351402","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617511,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140617511,"seq_region_name":"7","id":"rs1800126709","clinical_significance":[]},{"clinical_significance":[],"id":"rs1800126804","seq_region_name":"7","source":"dbSNP","start":140617512,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140617512,"alleles":["T","C"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140617514,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617514,"clinical_significance":[],"seq_region_name":"7","id":"rs1177955137"},{"seq_region_name":"7","id":"rs1385247955","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140617515,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617515,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1341119820","clinical_significance":[],"start":140617519,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140617519,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140617522,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617522,"clinical_significance":[],"id":"rs1800127359","seq_region_name":"7"},{"id":"rs1800127526","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140617532,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617532,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1800127678","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617533,"source":"dbSNP","strand":1,"feature_type":"variation","end":140617533,"alleles":["A","G"]},{"alleles":["T","A","C"],"end":140617534,"feature_type":"variation","strand":1,"source":"dbSNP","start":140617534,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs954671652","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140617541,"alleles":["AAA","AA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617539,"clinical_significance":[],"seq_region_name":"7","id":"rs1800128005"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140617540,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617540,"source":"dbSNP","seq_region_name":"7","id":"rs912050594","clinical_significance":[]},{"alleles":["C","T"],"end":140617543,"strand":1,"feature_type":"variation","start":140617543,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs986092987","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140617544,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617544,"clinical_significance":[],"seq_region_name":"7","id":"rs536209117"},{"feature_type":"variation","strand":1,"end":140617547,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617547,"clinical_significance":[],"id":"rs1405884220","seq_region_name":"7"},{"id":"rs555244564","seq_region_name":"7","clinical_significance":[],"start":140617550,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140617550,"strand":1,"feature_type":"variation"},{"start":140617557,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140617557,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs910580997","clinical_significance":[]},{"alleles":["C","T"],"end":140617559,"feature_type":"variation","strand":1,"source":"dbSNP","start":140617559,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1800129137","seq_region_name":"7"},{"source":"dbSNP","start":140617560,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140617560,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1800129302","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617561,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140617561,"clinical_significance":[],"seq_region_name":"7","id":"rs1800129458"},{"seq_region_name":"7","id":"rs1332383401","clinical_significance":[],"strand":1,"feature_type":"variation","end":140617563,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617563,"source":"dbSNP"},{"seq_region_name":"7","id":"rs943548432","clinical_significance":[],"start":140617564,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140617564,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617566,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140617566,"clinical_significance":[],"seq_region_name":"7","id":"rs1800129939"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617570,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140617570,"clinical_significance":[],"seq_region_name":"7","id":"rs969358137"},{"end":140617573,"alleles":["GGG","GG"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140617571,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1800130296"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617574,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140617574,"clinical_significance":[],"seq_region_name":"7","id":"rs2130714243"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1165770419","end":140617575,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140617575,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140617576,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617576,"clinical_significance":[],"seq_region_name":"7","id":"rs1800130605"},{"clinical_significance":[],"seq_region_name":"7","id":"rs191617669","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140617577,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617577},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617578,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140617578,"seq_region_name":"7","id":"rs979055621","clinical_significance":[]},{"seq_region_name":"7","id":"rs924742791","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617580,"source":"dbSNP","strand":1,"feature_type":"variation","end":140617580,"alleles":["C","G","T"]},{"seq_region_name":"7","id":"rs934821551","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140617581,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617581,"source":"dbSNP"},{"alleles":["T","A"],"end":140617582,"feature_type":"variation","strand":1,"source":"dbSNP","start":140617582,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1800131200"},{"feature_type":"variation","strand":1,"end":140617584,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617584,"clinical_significance":[],"seq_region_name":"7","id":"rs1185401787"},{"source":"dbSNP","start":140617586,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140617586,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1442634667"},{"seq_region_name":"7","id":"rs2130714297","clinical_significance":[],"alleles":["A","G"],"end":140617587,"strand":1,"feature_type":"variation","start":140617587,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs947003496","clinical_significance":[],"end":140617588,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140617588,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1199000080","feature_type":"variation","strand":1,"end":140617589,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617589},{"start":140617591,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140617591,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1439803710","clinical_significance":[]},{"alleles":["CCC","CC"],"end":140617598,"feature_type":"variation","strand":1,"source":"dbSNP","start":140617596,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1271211510"},{"seq_region_name":"7","id":"rs1331266816","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617598,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140617598},{"source":"dbSNP","start":140617599,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140617599,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1800132088"},{"seq_region_name":"7","id":"rs1800132193","clinical_significance":[],"strand":1,"feature_type":"variation","end":140617604,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617604,"source":"dbSNP"},{"end":140617605,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140617605,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1800132286","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585765515","source":"dbSNP","start":140617606,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140617606,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617607,"source":"dbSNP","strand":1,"feature_type":"variation","end":140617607,"alleles":["G","A"],"seq_region_name":"7","id":"rs1379981388","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800132601","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617608,"feature_type":"variation","strand":1,"end":140617608,"alleles":["G","A"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617609,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140617609,"clinical_significance":[],"seq_region_name":"7","id":"rs1317240263"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1397922896","end":140617611,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140617611,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1310824600","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617612,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140617612},{"seq_region_name":"7","id":"rs1042735041","clinical_significance":[],"alleles":["G","C","T"],"end":140617619,"strand":1,"feature_type":"variation","start":140617619,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["G","A","C"],"end":140617624,"feature_type":"variation","strand":1,"source":"dbSNP","start":140617624,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs534419496"},{"seq_region_name":"7","id":"rs1800133317","clinical_significance":[],"end":140617628,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140617628,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140617629,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617629,"clinical_significance":[],"seq_region_name":"7","id":"rs528174410"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617633,"feature_type":"variation","strand":1,"end":140617633,"alleles":["G","A"],"clinical_significance":[],"id":"rs998751252","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800133614","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617637,"feature_type":"variation","strand":1,"end":140617637,"alleles":["C","A"]},{"source":"dbSNP","start":140617646,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140617646,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1800133722"},{"seq_region_name":"7","id":"rs1800133821","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140617649,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617649,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs558919356","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617654,"feature_type":"variation","strand":1,"end":140617654,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs948486989","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617658,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140617658},{"strand":1,"feature_type":"variation","end":140617659,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617659,"source":"dbSNP","seq_region_name":"7","id":"rs1800134112","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617660,"source":"dbSNP","strand":1,"feature_type":"variation","end":140617660,"alleles":["G","C"],"seq_region_name":"7","id":"rs1800134210","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617663,"source":"dbSNP","strand":1,"feature_type":"variation","end":140617663,"alleles":["A","G"],"seq_region_name":"7","id":"rs2130714433","clinical_significance":[]},{"id":"rs1800134301","seq_region_name":"7","clinical_significance":[],"start":140617664,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140617664,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1044442421","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617668,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140617668},{"id":"rs1365671683","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140617669,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617669,"source":"dbSNP"},{"alleles":["C","T"],"end":140617670,"strand":1,"feature_type":"variation","start":140617670,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs577491832","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1035634244","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617671,"feature_type":"variation","strand":1,"end":140617671,"alleles":["A","G"]},{"feature_type":"variation","strand":1,"end":140617672,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617672,"clinical_significance":[],"seq_region_name":"7","id":"rs377382616"},{"alleles":["C","G"],"end":140617673,"strand":1,"feature_type":"variation","start":140617673,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1197857661","clinical_significance":[]},{"id":"rs1471063025","seq_region_name":"7","clinical_significance":[],"start":140617686,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140617686,"alleles":["C","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800135063","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617693,"feature_type":"variation","strand":1,"end":140617693,"alleles":["G","A","T"]},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140617694,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617694,"source":"dbSNP","seq_region_name":"7","id":"rs1800135177","clinical_significance":[]},{"id":"rs1243743396","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140617695,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617695,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1230959006","source":"dbSNP","start":140617699,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140617699,"alleles":["G","A"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140617700,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617700,"source":"dbSNP","seq_region_name":"7","id":"rs1585765708","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140617703,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617703,"clinical_significance":[],"id":"rs1181434728","seq_region_name":"7"},{"id":"rs1800135678","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617705,"source":"dbSNP","strand":1,"feature_type":"variation","end":140617705,"alleles":["C","A","T"]},{"alleles":["C","G"],"end":140617706,"strand":1,"feature_type":"variation","start":140617706,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1005860398","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1800135903","clinical_significance":[],"alleles":["A","G"],"end":140617714,"strand":1,"feature_type":"variation","start":140617714,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1483938124","seq_region_name":"7","clinical_significance":[],"alleles":["AAAA","AAAAA"],"end":140617717,"strand":1,"feature_type":"variation","start":140617714,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["AACAACAACAACAA","AACAACAACAA"],"end":140617729,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617716,"source":"dbSNP","seq_region_name":"7","id":"rs1294080046","clinical_significance":[]},{"seq_region_name":"7","id":"rs1179655627","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140617721,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617721,"source":"dbSNP"},{"clinical_significance":[],"id":"rs2130714533","seq_region_name":"7","source":"dbSNP","start":140617725,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140617725,"alleles":["A","G"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140617726,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140617726,"alleles":["A","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1358790724"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1036964568","end":140617727,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140617727,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1800136430","clinical_significance":[],"start":140617729,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140617729,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617730,"feature_type":"variation","strand":1,"end":140617730,"alleles":["A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1225965782"},{"alleles":["T","C"],"end":140617737,"feature_type":"variation","strand":1,"source":"dbSNP","start":140617737,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs545171344"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617744,"feature_type":"variation","strand":1,"end":140617744,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585765782"},{"start":140617747,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140617747,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1279274773","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617755,"source":"dbSNP","strand":1,"feature_type":"variation","end":140617755,"alleles":["A","-"],"seq_region_name":"7","id":"rs1441028683","clinical_significance":[]},{"clinical_significance":[],"id":"rs1585765807","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617759,"feature_type":"variation","strand":1,"end":140617759,"alleles":["A","C"]},{"clinical_significance":[],"id":"rs1345709209","seq_region_name":"7","source":"dbSNP","start":140617760,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140617760,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1585765828","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617761,"source":"dbSNP","strand":1,"feature_type":"variation","end":140617761,"alleles":["A","C"]},{"id":"rs1195415085","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140617764,"alleles":["CCT","CCTCCT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617762,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800137453","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140617763,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617763},{"clinical_significance":[],"seq_region_name":"7","id":"rs997977332","feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140617764,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617764},{"start":140617770,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G","T"],"end":140617770,"strand":1,"feature_type":"variation","id":"rs1800137686","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140617775,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617775,"source":"dbSNP","id":"rs557054023","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs575315367","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617776,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140617776},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617783,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140617783,"id":"rs1800138022","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617788,"source":"dbSNP","strand":1,"feature_type":"variation","end":140617788,"alleles":["C","A"],"seq_region_name":"7","id":"rs1464455214","clinical_significance":[]},{"id":"rs963802018","seq_region_name":"7","clinical_significance":[],"end":140617789,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140617789,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140617790,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140617790,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1402363093","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs766633882","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617794,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140617794},{"start":140617798,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140617798,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs542231467","seq_region_name":"7","clinical_significance":[]},{"start":140617808,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140617808,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","id":"rs561253580","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1585765907","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617820,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140617820},{"seq_region_name":"7","id":"rs1800138987","clinical_significance":[],"end":140617822,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140617822,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140617828,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140617828,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1480898547"},{"alleles":["A","G"],"end":140617832,"strand":1,"feature_type":"variation","start":140617832,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130714649","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800139079","source":"dbSNP","start":140617833,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140617833,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1007665725","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140617836,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617836,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140617838,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617838,"source":"dbSNP","seq_region_name":"7","id":"rs1800139270","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140617840,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617840,"source":"dbSNP","seq_region_name":"7","id":"rs1800139394","clinical_significance":[]},{"seq_region_name":"7","id":"rs142935736","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617841,"source":"dbSNP","strand":1,"feature_type":"variation","end":140617841,"alleles":["C","A","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1490225260","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617842,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140617842},{"start":140617846,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140617846,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs950747703","clinical_significance":[]},{"end":140617847,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140617847,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1218570591","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140617848,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617848,"clinical_significance":[],"seq_region_name":"7","id":"rs968761464"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1315579536","source":"dbSNP","start":140617848,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140617851,"alleles":["GATG","GATGATG"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140617850,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617850,"source":"dbSNP","seq_region_name":"7","id":"rs1800140171","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140617853,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617853,"source":"dbSNP","seq_region_name":"7","id":"rs1220131943","clinical_significance":[]},{"seq_region_name":"7","id":"rs1800140344","clinical_significance":[],"start":140617854,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140617854,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140617855,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140617855,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1800140462","seq_region_name":"7"},{"clinical_significance":[],"id":"rs183074473","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617864,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140617864},{"seq_region_name":"7","id":"rs1800140686","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617865,"source":"dbSNP","strand":1,"feature_type":"variation","end":140617865,"alleles":["A","G"]},{"id":"rs1800140796","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140617868,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617868,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800140898","alleles":["T","C"],"end":140617869,"feature_type":"variation","strand":1,"source":"dbSNP","start":140617869,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800140992","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140617870,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617870},{"clinical_significance":[],"seq_region_name":"7","id":"rs943513516","end":140617872,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140617872,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs975325731","source":"dbSNP","start":140617873,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140617873,"feature_type":"variation","strand":1},{"alleles":["A","G"],"end":140617874,"feature_type":"variation","strand":1,"source":"dbSNP","start":140617874,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs540500159"},{"id":"rs924889676","seq_region_name":"7","clinical_significance":[],"start":140617877,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140617877,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800141548","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617880,"feature_type":"variation","strand":1,"end":140617885,"alleles":["CTCACT","CT"]},{"seq_region_name":"7","id":"rs1563181149","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140617884,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617884,"source":"dbSNP"},{"id":"rs1344384390","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617889,"source":"dbSNP","strand":1,"feature_type":"variation","end":140617889,"alleles":["A","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1280339437","feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140617894,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617894},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617895,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140617895,"clinical_significance":[],"seq_region_name":"7","id":"rs956313829"},{"seq_region_name":"7","id":"rs564788224","clinical_significance":[],"start":140617896,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140617896,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs915448237","clinical_significance":[],"start":140617897,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140617897,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140617898,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617898,"source":"dbSNP","seq_region_name":"7","id":"rs1800142297","clinical_significance":[]},{"start":140617902,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140617902,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs1800142384","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140617910,"alleles":["TTTTTT","TTTTTTT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617905,"clinical_significance":[],"seq_region_name":"7","id":"rs1800142476"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617925,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140617925,"clinical_significance":[],"seq_region_name":"7","id":"rs1800142594"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617926,"feature_type":"variation","strand":1,"end":140617926,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1470160887"},{"end":140617928,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140617928,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130714835"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800142777","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617931,"feature_type":"variation","strand":1,"end":140617931,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1431150954","source":"dbSNP","start":140617932,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140617932,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs917452278","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617934,"feature_type":"variation","strand":1,"end":140617934,"alleles":["T","C"]},{"strand":1,"feature_type":"variation","end":140617935,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617935,"source":"dbSNP","id":"rs1800143083","seq_region_name":"7","clinical_significance":[]},{"end":140617936,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140617936,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs546645110","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140617942,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617942,"source":"dbSNP","seq_region_name":"7","id":"rs1800143276","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1480197026","alleles":["G","A"],"end":140617943,"feature_type":"variation","strand":1,"source":"dbSNP","start":140617943,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1328659993","end":140617946,"alleles":["T","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140617946,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs532168679","end":140617947,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140617947,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140617955,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140617955,"strand":1,"feature_type":"variation","id":"rs550667423","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1446527552","feature_type":"variation","strand":1,"end":140617956,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617956},{"clinical_significance":[],"seq_region_name":"7","id":"rs947116404","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617958,"feature_type":"variation","strand":1,"end":140617958,"alleles":["A","C","G"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617959,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140617959,"clinical_significance":[],"id":"rs1188313807","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1800144119","seq_region_name":"7","source":"dbSNP","start":140617960,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140617960,"alleles":["T","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1800144214","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140617962,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617962,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1800144325","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617963,"feature_type":"variation","strand":1,"end":140617963,"alleles":["T","C"]},{"source":"dbSNP","start":140617967,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140617967,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs61121025"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1279216003","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617971,"feature_type":"variation","strand":1,"end":140617971,"alleles":["C","T"]},{"strand":1,"feature_type":"variation","end":140617973,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617973,"source":"dbSNP","seq_region_name":"7","id":"rs1313920374","clinical_significance":[]},{"seq_region_name":"7","id":"rs1207974079","clinical_significance":[],"alleles":["T","C"],"end":140617976,"strand":1,"feature_type":"variation","start":140617976,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140617977,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617977,"clinical_significance":[],"seq_region_name":"7","id":"rs1800144846"},{"seq_region_name":"7","id":"rs1800144925","clinical_significance":[],"strand":1,"feature_type":"variation","end":140617980,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140617980,"source":"dbSNP"},{"seq_region_name":"7","id":"rs948434715","clinical_significance":[],"start":140617984,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140617984,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800145134","end":140617985,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140617985,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1800145238","clinical_significance":[],"start":140617987,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140617987,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1800145359","clinical_significance":[],"alleles":["A","C"],"end":140617991,"strand":1,"feature_type":"variation","start":140617991,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs902835298","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617992,"feature_type":"variation","strand":1,"end":140617992,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1585766282","clinical_significance":[],"alleles":["G","A"],"end":140617995,"strand":1,"feature_type":"variation","start":140617995,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140617997,"feature_type":"variation","strand":1,"end":140617997,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1800145687"},{"seq_region_name":"7","id":"rs1800145794","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140618005,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618005,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1211408370","clinical_significance":[],"start":140618010,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140618010,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800145988","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618012,"feature_type":"variation","strand":1,"alleles":["CC","C"],"end":140618013},{"clinical_significance":[],"seq_region_name":"7","id":"rs1462990681","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618016,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140618016},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618020,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140618020,"clinical_significance":[],"seq_region_name":"7","id":"rs2130714973"},{"clinical_significance":[],"seq_region_name":"7","id":"rs150402624","feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140618022,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618022},{"start":140618028,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140618028,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1221318533","clinical_significance":[]},{"start":140618031,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140618031,"alleles":["A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs909512639","clinical_significance":[]},{"end":140618033,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140618033,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1322314578"},{"source":"dbSNP","start":140618034,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140618041,"alleles":["AGAAGAAG","AGAAG"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1800146629","seq_region_name":"7"},{"start":140618035,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140618035,"strand":1,"feature_type":"variation","id":"rs138167325","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140618038,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618038,"source":"dbSNP","id":"rs2130715008","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1260666486","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618040,"source":"dbSNP","strand":1,"feature_type":"variation","end":140618040,"alleles":["A","C"]},{"id":"rs1037318027","seq_region_name":"7","clinical_significance":[],"start":140618043,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140618043,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800147034","feature_type":"variation","strand":1,"end":140618047,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618047},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140618051,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618051,"source":"dbSNP","seq_region_name":"7","id":"rs1193450036","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1426354837","feature_type":"variation","strand":1,"end":140618053,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618053},{"clinical_significance":[],"seq_region_name":"7","id":"rs1269590889","source":"dbSNP","start":140618058,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140618058,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs548252514","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618059,"source":"dbSNP","strand":1,"feature_type":"variation","end":140618059,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1012717126","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618063,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140618063},{"alleles":["A","G"],"end":140618072,"feature_type":"variation","strand":1,"source":"dbSNP","start":140618072,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1800147676"},{"seq_region_name":"7","id":"rs1334370303","clinical_significance":[],"start":140618073,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140618073,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618078,"source":"dbSNP","strand":1,"feature_type":"variation","end":140618078,"alleles":["T","C"],"seq_region_name":"7","id":"rs1800147998","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs755008996","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618079,"feature_type":"variation","strand":1,"end":140618079,"alleles":["T","C"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618084,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140618084,"seq_region_name":"7","id":"rs1355287728","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1313698140","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618086,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140618086},{"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140618093,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618093,"clinical_significance":[],"seq_region_name":"7","id":"rs1172777512"},{"start":140618096,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140618096,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1426859770","clinical_significance":[]},{"seq_region_name":"7","id":"rs1435379227","clinical_significance":[],"end":140618099,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140618099,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618104,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140618104,"clinical_significance":[],"id":"rs998093475","seq_region_name":"7"},{"end":140618105,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140618105,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs187944485","seq_region_name":"7","clinical_significance":[]},{"id":"rs1800149408","seq_region_name":"7","clinical_significance":[],"start":140618111,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140618111,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618113,"feature_type":"variation","strand":1,"end":140618113,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1446912206"},{"start":140618115,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140618115,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs899027924","clinical_significance":[]},{"end":140618117,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140618117,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs889634625"},{"seq_region_name":"7","id":"rs1420453953","clinical_significance":[],"alleles":["T","C"],"end":140618127,"strand":1,"feature_type":"variation","start":140618127,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs368169335","seq_region_name":"7","source":"dbSNP","start":140618130,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140618130,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618134,"source":"dbSNP","strand":1,"feature_type":"variation","end":140618134,"alleles":["C","T"],"seq_region_name":"7","id":"rs1251569630","clinical_significance":[]},{"seq_region_name":"7","id":"rs1026370755","clinical_significance":[],"start":140618141,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140618141,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140618142,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618142,"clinical_significance":[],"seq_region_name":"7","id":"rs1563181274"},{"alleles":["A","G"],"end":140618145,"strand":1,"feature_type":"variation","start":140618145,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130715160","clinical_significance":[]},{"id":"rs1800150734","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140618151,"strand":1,"feature_type":"variation","start":140618151,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1800150856","clinical_significance":[],"strand":1,"feature_type":"variation","end":140618155,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618155,"source":"dbSNP"},{"clinical_significance":[],"id":"rs191249893","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140618159,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618159},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140618165,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618165,"source":"dbSNP","seq_region_name":"7","id":"rs552901284","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618168,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140618168,"clinical_significance":[],"seq_region_name":"7","id":"rs987437694"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800151457","feature_type":"variation","strand":1,"end":140618170,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618170},{"clinical_significance":[],"seq_region_name":"7","id":"rs1399131546","feature_type":"variation","strand":1,"end":140618171,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618171},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618172,"source":"dbSNP","strand":1,"feature_type":"variation","end":140618172,"alleles":["T","C"],"seq_region_name":"7","id":"rs1585766575","clinical_significance":[]},{"clinical_significance":[],"id":"rs1312671351","seq_region_name":"7","alleles":["G","T"],"end":140618174,"feature_type":"variation","strand":1,"source":"dbSNP","start":140618174,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618180,"feature_type":"variation","strand":1,"end":140618180,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1800152046"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800152193","feature_type":"variation","strand":1,"end":140618184,"alleles":["A","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618184},{"start":140618185,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140618185,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1275178232","clinical_significance":[]},{"source":"dbSNP","start":140618187,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G","T"],"end":140618187,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1800152485"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618187,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AAA","AA"],"end":140618189,"id":"rs1369491892","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618191,"feature_type":"variation","strand":1,"end":140618191,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1217339416"},{"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140618192,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618192,"clinical_significance":[],"id":"rs1800152990","seq_region_name":"7"},{"id":"rs1017694195","seq_region_name":"7","clinical_significance":[],"alleles":["T","G"],"end":140618193,"strand":1,"feature_type":"variation","start":140618193,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140618196,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140618196,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1800153131","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140618199,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618199,"source":"dbSNP","id":"rs371589947","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585766629","clinical_significance":[],"end":140618202,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140618202,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1373754310","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","T"],"end":140618204,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618204,"source":"dbSNP"},{"end":140618205,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140618205,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1300587969"},{"seq_region_name":"7","id":"rs1800153848","clinical_significance":[],"start":140618206,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140618206,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140618216,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618216,"clinical_significance":[],"id":"rs969082522","seq_region_name":"7"},{"end":140618218,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140618218,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1460650317"},{"feature_type":"variation","strand":1,"end":140618219,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618219,"clinical_significance":[],"id":"rs1164220805","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140618224,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618224,"source":"dbSNP","seq_region_name":"7","id":"rs114656940","clinical_significance":[]},{"start":140618226,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140618226,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1383974773","clinical_significance":[]},{"seq_region_name":"7","id":"rs1800154763","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618227,"source":"dbSNP","strand":1,"feature_type":"variation","end":140618227,"alleles":["G","C"]},{"id":"rs182318148","seq_region_name":"7","clinical_significance":[],"start":140618228,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140618228,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs965325004","source":"dbSNP","start":140618229,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AAAA","AA"],"end":140618232,"feature_type":"variation","strand":1},{"alleles":["A","T"],"end":140618231,"feature_type":"variation","strand":1,"source":"dbSNP","start":140618231,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1800155222"},{"strand":1,"feature_type":"variation","end":140618232,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618232,"source":"dbSNP","seq_region_name":"7","id":"rs1800155357","clinical_significance":[]},{"start":140618234,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140618234,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1218228270","clinical_significance":[]},{"start":140618235,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140618235,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs2130715317","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1031710132","feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140618236,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618236},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618237,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140618237,"seq_region_name":"7","id":"rs1800155798","clinical_significance":[]},{"start":140618238,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TTT","TT"],"end":140618240,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130715335","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs777965669","source":"dbSNP","start":140618243,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140618243,"alleles":["T","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1253086301","seq_region_name":"7","source":"dbSNP","start":140618246,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140618246,"alleles":["T","A"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140618247,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618247,"source":"dbSNP","seq_region_name":"7","id":"rs1800156079","clinical_significance":[]},{"seq_region_name":"7","id":"rs1178585280","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618251,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140618251},{"alleles":["G","A"],"end":140618263,"feature_type":"variation","strand":1,"source":"dbSNP","start":140618263,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1563181349","seq_region_name":"7"},{"alleles":["T","C"],"end":140618264,"feature_type":"variation","strand":1,"source":"dbSNP","start":140618264,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1800156377"},{"id":"rs1585766732","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140618265,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618265,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618266,"source":"dbSNP","strand":1,"feature_type":"variation","end":140618266,"alleles":["T","G"],"seq_region_name":"7","id":"rs2130715365","clinical_significance":[]},{"clinical_significance":[],"id":"rs78798636","seq_region_name":"7","feature_type":"variation","strand":1,"end":140618270,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618270},{"alleles":["A","G"],"end":140618274,"feature_type":"variation","strand":1,"source":"dbSNP","start":140618274,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1479413918"},{"id":"rs568276049","seq_region_name":"7","clinical_significance":[],"start":140618276,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","T"],"end":140618276,"strand":1,"feature_type":"variation"},{"end":140618281,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140618281,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1222519637","clinical_significance":[]},{"clinical_significance":[],"id":"rs1800156925","seq_region_name":"7","alleles":["G","A"],"end":140618282,"feature_type":"variation","strand":1,"source":"dbSNP","start":140618282,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140618286,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140618286,"alleles":["A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1360952122","clinical_significance":[]},{"end":140618290,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140618290,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130715395"},{"clinical_significance":[],"seq_region_name":"7","id":"rs993105494","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618291,"feature_type":"variation","strand":1,"end":140618291,"alleles":["C","G","T"]},{"end":140618295,"alleles":["CTTTT","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140618291,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1800157258"},{"seq_region_name":"7","id":"rs975060498","clinical_significance":[],"end":140618296,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140618296,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140618297,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618297,"source":"dbSNP","id":"rs1800157535","seq_region_name":"7","clinical_significance":[]},{"start":140618299,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140618299,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs915375314","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800157774","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618303,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140618303},{"seq_region_name":"7","id":"rs1800157851","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618314,"source":"dbSNP","strand":1,"feature_type":"variation","end":140618314,"alleles":["A","G"]},{"end":140618318,"alleles":["C","A","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140618318,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1308805302"},{"clinical_significance":[],"id":"rs1024457864","seq_region_name":"7","source":"dbSNP","start":140618319,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140618319,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140618320,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618320,"source":"dbSNP","seq_region_name":"7","id":"rs1800158432","clinical_significance":[]},{"alleles":["A","G"],"end":140618326,"feature_type":"variation","strand":1,"source":"dbSNP","start":140618326,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585766823"},{"start":140618327,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140618329,"alleles":["GGG","GGGG"],"strand":1,"feature_type":"variation","id":"rs1800158715","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140618328,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618328,"source":"dbSNP","id":"rs1800158852","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1389895373","clinical_significance":[],"end":140618337,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140618337,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140618338,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618338,"clinical_significance":[],"seq_region_name":"7","id":"rs970267704"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618346,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140618346,"clinical_significance":[],"seq_region_name":"7","id":"rs767496124"},{"start":140618349,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140618349,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs946894026","clinical_significance":[]},{"source":"dbSNP","start":140618350,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140618350,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1406885106"},{"feature_type":"variation","strand":1,"end":140618352,"alleles":["TTT","TT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618350,"clinical_significance":[],"id":"rs745478634","seq_region_name":"7"},{"start":140618365,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140618365,"alleles":["A","G"],"strand":1,"feature_type":"variation","id":"rs1800159930","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618366,"source":"dbSNP","strand":1,"feature_type":"variation","end":140618366,"alleles":["T","C"],"id":"rs1800160063","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140618367,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140618367,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs375569890"},{"seq_region_name":"7","id":"rs2130715545","clinical_significance":[],"alleles":["T","G"],"end":140618373,"strand":1,"feature_type":"variation","start":140618373,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800160335","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140618375,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618375},{"alleles":["G","C"],"end":140618376,"feature_type":"variation","strand":1,"source":"dbSNP","start":140618376,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1163572478"},{"seq_region_name":"7","id":"rs187901498","clinical_significance":[],"alleles":["C","T"],"end":140618382,"strand":1,"feature_type":"variation","start":140618382,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1454708701","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618383,"feature_type":"variation","strand":1,"alleles":["TT","TTTT"],"end":140618384},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140618385,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618385,"clinical_significance":[],"id":"rs1585766940","seq_region_name":"7"},{"alleles":["C","T"],"end":140618387,"feature_type":"variation","strand":1,"source":"dbSNP","start":140618387,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs575377665"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1157319523","feature_type":"variation","strand":1,"end":140618389,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618389},{"seq_region_name":"7","id":"rs1800161194","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618390,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140618390},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618391,"feature_type":"variation","strand":1,"end":140618391,"alleles":["G","C"],"clinical_significance":[],"id":"rs1416959910","seq_region_name":"7"},{"start":140618392,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140618392,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1250674432","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800161648","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140618398,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618398},{"id":"rs1800161800","seq_region_name":"7","clinical_significance":[],"start":140618400,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140618400,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140618403,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140618403,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1800161978"},{"strand":1,"feature_type":"variation","end":140618404,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618404,"source":"dbSNP","seq_region_name":"7","id":"rs1800162130","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs757211522","source":"dbSNP","start":140618405,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140618405,"alleles":["C","A","T"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140618406,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618406,"clinical_significance":[],"seq_region_name":"7","id":"rs972419338"},{"clinical_significance":[],"id":"rs2130715625","seq_region_name":"7","end":140618411,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140618411,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140618412,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618412,"source":"dbSNP","seq_region_name":"7","id":"rs1189975038","clinical_significance":[]},{"id":"rs35804526","seq_region_name":"7","clinical_significance":[],"end":140618416,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140618416,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1800162863","seq_region_name":"7","clinical_significance":[],"start":140618422,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140618422,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"alleles":["C","T"],"end":140618424,"feature_type":"variation","strand":1,"source":"dbSNP","start":140618424,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1800162961","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs918275046","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618425,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140618425},{"clinical_significance":[],"id":"rs1440370603","seq_region_name":"7","end":140618431,"alleles":["TTTTT","TTTTTT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140618427,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1160573779","clinical_significance":[],"start":140618430,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140618430,"alleles":["T","G"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140618440,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618440,"source":"dbSNP","seq_region_name":"7","id":"rs2130715662","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618441,"feature_type":"variation","strand":1,"end":140618441,"alleles":["C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1378577503"},{"seq_region_name":"7","id":"rs144269685","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618446,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140618446},{"alleles":["A","G"],"end":140618455,"feature_type":"variation","strand":1,"source":"dbSNP","start":140618455,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs554298069"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618457,"feature_type":"variation","strand":1,"end":140618457,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1328202059"},{"source":"dbSNP","start":140618466,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140618466,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs898975438"},{"seq_region_name":"7","id":"rs1800163771","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618468,"source":"dbSNP","strand":1,"feature_type":"variation","end":140618468,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs994648351","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140618469,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618469},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618470,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140618470,"id":"rs1800163951","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140618473,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TTTTTTT","TTTTTT"],"end":140618479,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1324460094"},{"seq_region_name":"7","id":"rs1800164124","clinical_significance":[],"alleles":["T","C"],"end":140618478,"strand":1,"feature_type":"variation","start":140618478,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618480,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140618480,"seq_region_name":"7","id":"rs1800164230","clinical_significance":[]},{"alleles":["GA","-"],"end":140618483,"strand":1,"feature_type":"variation","start":140618482,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1351401384","clinical_significance":[]},{"seq_region_name":"7","id":"rs1050979328","clinical_significance":[],"strand":1,"feature_type":"variation","end":140618488,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618488,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130715715","feature_type":"variation","strand":1,"alleles":["CC","C"],"end":140618498,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618497},{"id":"rs1800164651","seq_region_name":"7","clinical_significance":[],"start":140618502,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140618502,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1800164751","clinical_significance":[],"strand":1,"feature_type":"variation","end":140618504,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618504,"source":"dbSNP"},{"id":"rs572796268","seq_region_name":"7","clinical_significance":[],"alleles":["A","T"],"end":140618505,"strand":1,"feature_type":"variation","start":140618505,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["G","A"],"end":140618510,"feature_type":"variation","strand":1,"source":"dbSNP","start":140618510,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1292850811"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800165187","source":"dbSNP","start":140618519,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140618519,"alleles":["T","C"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140618525,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140618525,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130715741"},{"source":"dbSNP","start":140618530,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140618530,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1287606057","seq_region_name":"7"},{"start":140618531,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140618531,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585767115","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130715756","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618532,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140618532},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140618533,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618533,"source":"dbSNP","seq_region_name":"7","id":"rs1800165646","clinical_significance":[]},{"start":140618545,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140618545,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs1800165798","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140618549,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618549,"source":"dbSNP","seq_region_name":"7","id":"rs1453549100","clinical_significance":[]},{"end":140618551,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140618551,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1800165937","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1377608972","source":"dbSNP","start":140618552,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140618552,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140618562,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618562,"clinical_significance":[],"seq_region_name":"7","id":"rs1430426555"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1176786583","source":"dbSNP","start":140618579,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140618579,"alleles":["T","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1009018956","source":"dbSNP","start":140618582,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A","C"],"end":140618582,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs778741817","clinical_significance":[],"alleles":["C","T"],"end":140618584,"strand":1,"feature_type":"variation","start":140618584,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs964763788","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140618585,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618585},{"seq_region_name":"7","id":"rs1429072806","clinical_significance":[],"start":140618589,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140618589,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs996816527","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140618593,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618593,"source":"dbSNP"},{"end":140618594,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140618594,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs942548855","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585767199","feature_type":"variation","strand":1,"end":140618595,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618595},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140618596,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618596,"clinical_significance":[],"seq_region_name":"7","id":"rs1043990059"},{"end":140618597,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140618597,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1306398582","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1263466126","clinical_significance":[],"end":140618602,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140618602,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140618608,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618608,"clinical_significance":[],"id":"rs1359620845","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs904597702","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618611,"feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140618611},{"clinical_significance":[],"seq_region_name":"7","id":"rs377234411","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140618613,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618613},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618614,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140618614,"seq_region_name":"7","id":"rs1352357349","clinical_significance":[]},{"alleles":["A","G"],"end":140618616,"feature_type":"variation","strand":1,"source":"dbSNP","start":140618616,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1800168826"},{"seq_region_name":"7","id":"rs1800168967","clinical_significance":[],"end":140618620,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140618620,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["G","C"],"end":140618622,"strand":1,"feature_type":"variation","start":140618622,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1022564781","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618624,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140618624,"clinical_significance":[],"seq_region_name":"7","id":"rs968184542"},{"start":140618625,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140618625,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1328241526","clinical_significance":[]},{"id":"rs978259145","seq_region_name":"7","clinical_significance":[],"end":140618626,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140618626,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs924322059","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140618629,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618629},{"source":"dbSNP","start":140618632,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140618632,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1407320592"},{"seq_region_name":"7","id":"rs955765953","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618633,"source":"dbSNP","strand":1,"feature_type":"variation","end":140618633,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1323862816","clinical_significance":[],"end":140618636,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140618636,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140618643,"alleles":["TCATCAT","TCAT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140618637,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1800170175","seq_region_name":"7"},{"start":140618638,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140618638,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1403384309","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618643,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140618643,"clinical_significance":[],"seq_region_name":"7","id":"rs1219885518"},{"clinical_significance":[],"seq_region_name":"7","id":"rs992616346","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618645,"feature_type":"variation","strand":1,"end":140618645,"alleles":["A","G"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618646,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140618646,"clinical_significance":[],"id":"rs1000715887","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1252884760","feature_type":"variation","strand":1,"end":140618647,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618647},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618648,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140618648,"clinical_significance":[],"seq_region_name":"7","id":"rs1458573733"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140618650,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618650,"source":"dbSNP","id":"rs1448724450","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs540201264","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618662,"feature_type":"variation","strand":1,"end":140618662,"alleles":["T","C"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618663,"source":"dbSNP","strand":1,"feature_type":"variation","end":140618663,"alleles":["C","T"],"seq_region_name":"7","id":"rs1185145353","clinical_significance":[]},{"seq_region_name":"7","id":"rs1459794344","clinical_significance":[],"end":140618665,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140618665,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1800172002","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618669,"feature_type":"variation","strand":1,"end":140618669,"alleles":["T","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800172154","end":140618672,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140618672,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140618679,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618679,"source":"dbSNP","seq_region_name":"7","id":"rs1278233043","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800172427","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140618684,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618684},{"source":"dbSNP","start":140618689,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140618689,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1800172574"},{"start":140618693,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140618693,"alleles":["C","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1196600265","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1236370787","alleles":["C","T"],"end":140618699,"feature_type":"variation","strand":1,"source":"dbSNP","start":140618699,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs574453134","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618702,"source":"dbSNP","strand":1,"feature_type":"variation","end":140618702,"alleles":["C","T"]},{"id":"rs1469752073","seq_region_name":"7","clinical_significance":[],"start":140618704,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140618704,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs564794492","clinical_significance":[],"start":140618706,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140618706,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs891821946","clinical_significance":[],"alleles":["T","C"],"end":140618712,"strand":1,"feature_type":"variation","start":140618712,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1800173538","clinical_significance":[],"start":140618721,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140618721,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"start":140618726,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140618726,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs916888626","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140618731,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618731,"source":"dbSNP","id":"rs948426885","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1317638855","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["TAAGT","T"],"end":140618735,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618731,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800173925","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140618735,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618735},{"seq_region_name":"7","id":"rs1416294447","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618740,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140618740},{"clinical_significance":[],"seq_region_name":"7","id":"rs1044682151","alleles":["G","A"],"end":140618743,"feature_type":"variation","strand":1,"source":"dbSNP","start":140618743,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618750,"feature_type":"variation","strand":1,"alleles":["TTTTTT","TTTTT"],"end":140618755,"clinical_significance":[],"id":"rs372640446","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1014486481","source":"dbSNP","start":140618754,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140618754,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1400786541","clinical_significance":[],"start":140618760,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140618760,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1448822691","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140618761,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618761,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1429054930","clinical_significance":[],"strand":1,"feature_type":"variation","end":140618762,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618762,"source":"dbSNP"},{"alleles":["TTTTTTT","TTTTTTTT"],"end":140618778,"strand":1,"feature_type":"variation","start":140618772,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1329228089","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs930446962","seq_region_name":"7","source":"dbSNP","start":140618780,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140618780,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1047548404","alleles":["G","A"],"end":140618781,"feature_type":"variation","strand":1,"source":"dbSNP","start":140618781,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140618782,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140618782,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1236669061"},{"end":140618782,"alleles":["-","A","AT"],"strand":1,"feature_type":"variation","start":140618783,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1285571159","clinical_significance":[]},{"seq_region_name":"7","id":"rs1182818379","clinical_significance":[],"strand":1,"feature_type":"variation","end":140618783,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618783,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140618783,"alleles":["-","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618784,"source":"dbSNP","seq_region_name":"7","id":"rs1353872315","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618785,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140618785,"seq_region_name":"7","id":"rs1227419466","clinical_significance":[]},{"clinical_significance":[],"id":"rs1248549534","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618788,"feature_type":"variation","strand":1,"end":140618788,"alleles":["T","C"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618789,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140618789,"seq_region_name":"7","id":"rs1204468317","clinical_significance":[]},{"id":"rs1800175734","seq_region_name":"7","clinical_significance":[],"end":140618793,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140618793,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618794,"source":"dbSNP","strand":1,"feature_type":"variation","end":140618794,"alleles":["T","C"],"seq_region_name":"7","id":"rs1800175828","clinical_significance":[]},{"seq_region_name":"7","id":"rs1800175923","clinical_significance":[],"end":140618795,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140618795,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140618796,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140618796,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1800176013","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140618797,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618797,"source":"dbSNP","seq_region_name":"7","id":"rs1800176115","clinical_significance":[]},{"clinical_significance":[],"id":"rs1360233636","seq_region_name":"7","end":140618802,"alleles":["CC","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140618801,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618802,"feature_type":"variation","strand":1,"end":140618802,"alleles":["C","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1294640856"},{"start":140618803,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140618803,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1280432810","clinical_significance":[]},{"source":"dbSNP","start":140618803,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140618813,"alleles":["TTTTTTTTTTT","TTTTTTTTTT","TTTTTTTTTTTT","TTTTTTTTTTTTT","TTTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTTT"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs886314678"},{"start":140618807,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140618807,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1800176734","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140618808,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618808,"clinical_significance":[],"seq_region_name":"7","id":"rs1800176827"},{"feature_type":"variation","strand":1,"end":140618809,"alleles":["T","A","C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618809,"clinical_significance":[],"id":"rs576628545","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618812,"feature_type":"variation","strand":1,"end":140618812,"alleles":["T","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1319051804"},{"start":140618813,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["TCT","T"],"end":140618815,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1491299323","clinical_significance":[]},{"seq_region_name":"7","id":"rs1201069922","clinical_significance":[],"start":140618814,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140618814,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1365652976","clinical_significance":[],"start":140618814,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","-"],"end":140618814,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1491470913","feature_type":"variation","strand":1,"alleles":["C","CC"],"end":140618814,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618814},{"seq_region_name":"7","id":"rs2130716178","clinical_significance":[],"alleles":["T","C"],"end":140618815,"strand":1,"feature_type":"variation","start":140618815,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140618818,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140618818,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1403480597","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1412808155","clinical_significance":[],"strand":1,"feature_type":"variation","end":140618819,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618819,"source":"dbSNP"},{"source":"dbSNP","start":140618820,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140618820,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1256776319"},{"seq_region_name":"7","id":"rs1437291561","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140618822,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618822,"source":"dbSNP"},{"start":140618826,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140618826,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs970594273","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140618827,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618827,"clinical_significance":[],"seq_region_name":"7","id":"rs1800178091"},{"feature_type":"variation","strand":1,"end":140618833,"alleles":["T","A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618833,"clinical_significance":[],"id":"rs543972872","seq_region_name":"7"},{"seq_region_name":"7","id":"rs900471170","clinical_significance":[],"start":140618835,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140618835,"strand":1,"feature_type":"variation"},{"start":140618841,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140618841,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1563181604","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618842,"feature_type":"variation","strand":1,"end":140618842,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1017555958"},{"clinical_significance":[],"seq_region_name":"7","id":"rs962480442","feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140618843,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618843},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800178722","alleles":["G","C"],"end":140618849,"feature_type":"variation","strand":1,"source":"dbSNP","start":140618849,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140618850,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140618850,"strand":1,"feature_type":"variation","id":"rs1800178877","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1285415552","end":140618851,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140618851,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1800179142","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618852,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140618852},{"seq_region_name":"7","id":"rs74833407","clinical_significance":[],"start":140618859,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140618859,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1348944286","clinical_significance":[],"alleles":["G","A"],"end":140618862,"strand":1,"feature_type":"variation","start":140618862,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140618864,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140618864,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs918222452","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130716272","source":"dbSNP","start":140618865,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140618865,"alleles":["A","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1423984100","end":140618868,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140618868,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140618874,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140618874,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1800180094"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618885,"source":"dbSNP","strand":1,"feature_type":"variation","end":140618885,"alleles":["G","C"],"id":"rs1800180261","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","C","G"],"end":140618888,"strand":1,"feature_type":"variation","start":140618888,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs530168828","seq_region_name":"7","clinical_significance":[]},{"alleles":["C","T"],"end":140618890,"feature_type":"variation","strand":1,"source":"dbSNP","start":140618890,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1227381580"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800180613","source":"dbSNP","start":140618891,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140618891,"alleles":["C","T"],"feature_type":"variation","strand":1},{"id":"rs548639865","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140618892,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618892,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1800180845","clinical_significance":[],"start":140618892,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["GGG","GG"],"end":140618894,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618895,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140618895,"seq_region_name":"7","id":"rs1800180941","clinical_significance":[]},{"id":"rs1800181041","seq_region_name":"7","clinical_significance":[],"start":140618898,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140618898,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140618899,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618899,"source":"dbSNP","seq_region_name":"7","id":"rs866977687","clinical_significance":[]},{"alleles":["G","A","C"],"end":140618900,"feature_type":"variation","strand":1,"source":"dbSNP","start":140618900,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs111390456"},{"clinical_significance":[],"id":"rs1800181401","seq_region_name":"7","alleles":["C","G"],"end":140618901,"feature_type":"variation","strand":1,"source":"dbSNP","start":140618901,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800181511","alleles":["C","A"],"end":140618906,"feature_type":"variation","strand":1,"source":"dbSNP","start":140618906,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140618908,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618908,"clinical_significance":[],"seq_region_name":"7","id":"rs778453297"},{"clinical_significance":[],"id":"rs192862056","seq_region_name":"7","feature_type":"variation","strand":1,"end":140618909,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618909},{"id":"rs373482244","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140618910,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618910,"source":"dbSNP"},{"alleles":["CTCCAGAGTAGCTGGGACTATAGGCGCCCGCCTCCACGCCCAGCT","CT"],"end":140618963,"feature_type":"variation","strand":1,"source":"dbSNP","start":140618919,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1800182464"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618921,"source":"dbSNP","strand":1,"feature_type":"variation","end":140618921,"alleles":["C","T"],"seq_region_name":"7","id":"rs2130716400","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618923,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140618923,"clinical_significance":[],"id":"rs903709058","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140618926,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618926,"clinical_significance":[],"seq_region_name":"7","id":"rs1480846492"},{"clinical_significance":[],"seq_region_name":"7","id":"rs746665273","source":"dbSNP","start":140618929,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C","T"],"end":140618929,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140618933,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140618933,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1800183051","seq_region_name":"7"},{"clinical_significance":[],"id":"rs936077504","seq_region_name":"7","source":"dbSNP","start":140618935,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140618935,"alleles":["A","G"],"feature_type":"variation","strand":1},{"end":140618939,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140618939,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1800183236","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140618941,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618941,"clinical_significance":[],"seq_region_name":"7","id":"rs1800183327"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618943,"source":"dbSNP","strand":1,"feature_type":"variation","end":140618943,"alleles":["C","A","T"],"id":"rs1431577617","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1800183525","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618944,"source":"dbSNP","strand":1,"feature_type":"variation","end":140618944,"alleles":["G","A"]},{"id":"rs752337977","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140618945,"strand":1,"feature_type":"variation","start":140618945,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140618947,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140618947,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1053207422"},{"source":"dbSNP","start":140618948,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140618948,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1243240041"},{"end":140618949,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140618949,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130716425","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618952,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140618952,"id":"rs1800183929","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1218553129","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140618953,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618953},{"strand":1,"feature_type":"variation","end":140618954,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618954,"source":"dbSNP","seq_region_name":"7","id":"rs1445692646","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs552907750","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140618955,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618955},{"clinical_significance":[],"id":"rs917023920","seq_region_name":"7","feature_type":"variation","strand":1,"end":140618956,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618956},{"clinical_significance":[],"seq_region_name":"7","id":"rs1323755188","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140618961,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618961},{"alleles":["TTTTTT","TTTTTTT"],"end":140618971,"strand":1,"feature_type":"variation","start":140618966,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1284672733","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618968,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140618968,"clinical_significance":[],"seq_region_name":"7","id":"rs1800184670"},{"feature_type":"variation","strand":1,"end":140618970,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618970,"clinical_significance":[],"id":"rs1800184777","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800184869","alleles":["T","C"],"end":140618973,"feature_type":"variation","strand":1,"source":"dbSNP","start":140618973,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140618974,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618974,"clinical_significance":[],"seq_region_name":"7","id":"rs1217022571"},{"id":"rs1366254327","seq_region_name":"7","clinical_significance":[],"start":140618975,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140618975,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140618975,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TTTTTT","TTTTT"],"end":140618980,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1800185177"},{"id":"rs2130716522","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140618980,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618980,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800185286","feature_type":"variation","strand":1,"alleles":["G","-"],"end":140618981,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140618981},{"seq_region_name":"7","id":"rs1800185376","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618988,"source":"dbSNP","strand":1,"feature_type":"variation","end":140618988,"alleles":["T","C"]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140618999,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140618999,"source":"dbSNP","id":"rs2130716536","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140619000,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140619000,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs184849837","seq_region_name":"7"},{"id":"rs1800185594","seq_region_name":"7","clinical_significance":[],"end":140619001,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140619001,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140619003,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140619003,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1800185696","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1432796146","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619005,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140619005},{"seq_region_name":"7","id":"rs979802829","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619008,"source":"dbSNP","strand":1,"feature_type":"variation","end":140619008,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1319594650","end":140619017,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140619017,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619018,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140619018,"clinical_significance":[],"id":"rs2130716569","seq_region_name":"7"},{"clinical_significance":[],"id":"rs776061327","seq_region_name":"7","source":"dbSNP","start":140619019,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140619019,"alleles":["C","T"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140619020,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619020,"clinical_significance":[],"seq_region_name":"7","id":"rs1024353287"},{"id":"rs748682904","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140619022,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619022,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619024,"source":"dbSNP","strand":1,"feature_type":"variation","end":140619024,"alleles":["T","C"],"seq_region_name":"7","id":"rs1800186438","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140619030,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619030,"clinical_significance":[],"id":"rs376643914","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1414044856","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619033,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140619033},{"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140619034,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619034,"source":"dbSNP","id":"rs374211614","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800186849","alleles":["T","C"],"end":140619035,"feature_type":"variation","strand":1,"source":"dbSNP","start":140619035,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1800186948","seq_region_name":"7","source":"dbSNP","start":140619042,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140619042,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619044,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140619044,"clinical_significance":[],"seq_region_name":"7","id":"rs538457221"},{"seq_region_name":"7","id":"rs1247833896","clinical_significance":[],"end":140619045,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140619045,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs550432406","clinical_significance":[],"end":140619049,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140619049,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140619050,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140619050,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs563228155","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619055,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140619055,"clinical_significance":[],"seq_region_name":"7","id":"rs1585768228"},{"end":140619066,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140619066,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1264666707"},{"alleles":["A","T"],"end":140619069,"feature_type":"variation","strand":1,"source":"dbSNP","start":140619069,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1800187493"},{"seq_region_name":"7","id":"rs963214873","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619074,"source":"dbSNP","strand":1,"feature_type":"variation","end":140619074,"alleles":["A","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619078,"source":"dbSNP","strand":1,"feature_type":"variation","end":140619078,"alleles":["A","G"],"seq_region_name":"7","id":"rs1311168374","clinical_significance":[]},{"alleles":["T","A","C"],"end":140619079,"feature_type":"variation","strand":1,"source":"dbSNP","start":140619079,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1800187749"},{"clinical_significance":[],"id":"rs1800187868","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619080,"feature_type":"variation","strand":1,"end":140619080,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1800187970","clinical_significance":[],"end":140619081,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140619081,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140619082,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140619082,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1800188054","clinical_significance":[]},{"start":140619087,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140619087,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs1273029996","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs763251074","clinical_significance":[],"alleles":["G","A","C"],"end":140619088,"strand":1,"feature_type":"variation","start":140619088,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1296748839","clinical_significance":[],"start":140619089,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140619089,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140619090,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140619090,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs771312167"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140619093,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619093,"clinical_significance":[],"seq_region_name":"7","id":"rs1025348544"},{"alleles":["G","A"],"end":140619094,"feature_type":"variation","strand":1,"source":"dbSNP","start":140619094,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs774487895"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1447496885","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140619095,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619095},{"seq_region_name":"7","id":"rs1800189037","clinical_significance":[],"alleles":["C","A","T"],"end":140619096,"strand":1,"feature_type":"variation","start":140619096,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140619097,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140619097,"strand":1,"feature_type":"variation","id":"rs758064703","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800189254","feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140619099,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619099},{"seq_region_name":"7","id":"rs1210429510","clinical_significance":[],"strand":1,"feature_type":"variation","end":140619102,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619102,"source":"dbSNP"},{"start":140619104,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140619104,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1800189441","clinical_significance":[]},{"source":"dbSNP","start":140619105,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140619105,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1800189528","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140619108,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619108,"source":"dbSNP","seq_region_name":"7","id":"rs1800189625","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140619111,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619111,"clinical_significance":[],"seq_region_name":"7","id":"rs1172573470"},{"clinical_significance":[],"id":"rs1428407213","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619113,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140619113},{"seq_region_name":"7","id":"rs1390156441","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619119,"source":"dbSNP","strand":1,"feature_type":"variation","end":140619119,"alleles":["T","C"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619122,"source":"dbSNP","strand":1,"feature_type":"variation","end":140619122,"alleles":["G","C"],"id":"rs955163294","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140619123,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619123,"clinical_significance":[],"seq_region_name":"7","id":"rs1264248768"},{"clinical_significance":[],"id":"rs2130716750","seq_region_name":"7","feature_type":"variation","strand":1,"end":140619130,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619130},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140619134,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619134,"source":"dbSNP","seq_region_name":"7","id":"rs1563181737","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140619136,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619136,"source":"dbSNP","seq_region_name":"7","id":"rs2130716759","clinical_significance":[]},{"seq_region_name":"7","id":"rs1164744444","clinical_significance":[],"start":140619137,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C","G"],"end":140619137,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1446896540","clinical_significance":[],"end":140619145,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140619145,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130716772","feature_type":"variation","strand":1,"end":140619149,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619149},{"start":140619157,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140619157,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs569220736","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800190652","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619160,"feature_type":"variation","strand":1,"alleles":["TTT","TT"],"end":140619162},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800190760","end":140619161,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140619161,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619162,"source":"dbSNP","strand":1,"feature_type":"variation","end":140619162,"alleles":["T","C"],"seq_region_name":"7","id":"rs568618868","clinical_significance":[]},{"seq_region_name":"7","id":"rs986421601","clinical_significance":[],"start":140619163,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140619163,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1179773219","seq_region_name":"7","source":"dbSNP","start":140619167,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140619167,"alleles":["A","G"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619169,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140619169,"clinical_significance":[],"id":"rs1482699932","seq_region_name":"7"},{"alleles":["T","G"],"end":140619172,"strand":1,"feature_type":"variation","start":140619172,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1478669711","clinical_significance":[]},{"source":"dbSNP","start":140619176,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140619176,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1232972565"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585768479","alleles":["G","A"],"end":140619181,"feature_type":"variation","strand":1,"source":"dbSNP","start":140619181,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140619183,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619183,"clinical_significance":[],"seq_region_name":"7","id":"rs2061155248"},{"source":"dbSNP","start":140619185,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140619185,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs536009749","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1800191732","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619189,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140619189},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800191831","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619191,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140619191},{"feature_type":"variation","strand":1,"end":140619192,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619192,"clinical_significance":[],"seq_region_name":"7","id":"rs1585768496"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140619194,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619194,"source":"dbSNP","seq_region_name":"7","id":"rs1206738291","clinical_significance":[]},{"end":140619196,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140619196,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1339403094","clinical_significance":[]},{"seq_region_name":"7","id":"rs1273914909","clinical_significance":[],"strand":1,"feature_type":"variation","end":140619197,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619197,"source":"dbSNP"},{"id":"rs1800192273","seq_region_name":"7","clinical_significance":[],"start":140619197,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AAAA","AAA"],"end":140619200,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1191289908","source":"dbSNP","start":140619209,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140619209,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619212,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140619212,"clinical_significance":[],"id":"rs2130716866","seq_region_name":"7"},{"end":140619214,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","start":140619214,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1246607579","clinical_significance":[]},{"source":"dbSNP","start":140619219,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140619219,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs910907204"},{"feature_type":"variation","strand":1,"end":140619223,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619223,"clinical_significance":[],"seq_region_name":"7","id":"rs1310230333"},{"clinical_significance":[],"id":"rs1800192962","seq_region_name":"7","feature_type":"variation","strand":1,"end":140619224,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619224},{"start":140619225,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140619225,"alleles":["C","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130716894","clinical_significance":[]},{"source":"dbSNP","start":140619228,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A","C"],"end":140619228,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1800193066"},{"source":"dbSNP","start":140619235,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140619235,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1395703005"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619239,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140619239,"seq_region_name":"7","id":"rs1800193288","clinical_significance":[]},{"clinical_significance":[],"id":"rs1800193387","seq_region_name":"7","alleles":["T","C"],"end":140619241,"feature_type":"variation","strand":1,"source":"dbSNP","start":140619241,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140619243,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619243,"source":"dbSNP","seq_region_name":"7","id":"rs190043671","clinical_significance":[]},{"source":"dbSNP","start":140619248,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140619248,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs963974285","seq_region_name":"7"},{"source":"dbSNP","start":140619256,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140619256,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1800193657"},{"clinical_significance":[],"seq_region_name":"7","id":"rs979777230","feature_type":"variation","strand":1,"end":140619259,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619259},{"seq_region_name":"7","id":"rs2130716943","clinical_significance":[],"start":140619262,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AGTGGAATACA","-"],"end":140619272,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1300093972","clinical_significance":[],"start":140619263,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140619263,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140619279,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","-"],"end":140619279,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs539446349"},{"seq_region_name":"7","id":"rs1800194061","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140619281,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619281,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800194165","end":140619284,"alleles":["GG","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140619283,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs2130716964","clinical_significance":[],"strand":1,"feature_type":"variation","end":140619288,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619288,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619290,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140619290,"clinical_significance":[],"id":"rs1370026894","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1800194376","clinical_significance":[],"start":140619292,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140619292,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619295,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140619295,"clinical_significance":[],"id":"rs925112319","seq_region_name":"7"},{"seq_region_name":"7","id":"rs192990377","clinical_significance":[],"start":140619296,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140619296,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1367094487","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619297,"feature_type":"variation","strand":1,"end":140619308,"alleles":["TAAATTAAATTA","TAAATTA"]},{"feature_type":"variation","strand":1,"end":140619298,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619298,"clinical_significance":[],"seq_region_name":"7","id":"rs1800194749"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140619305,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619305,"source":"dbSNP","id":"rs1800194856","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1800194963","seq_region_name":"7","alleles":["TTATGTTTA","TTA"],"end":140619314,"feature_type":"variation","strand":1,"source":"dbSNP","start":140619306,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619308,"source":"dbSNP","strand":1,"feature_type":"variation","end":140619308,"alleles":["A","C"],"seq_region_name":"7","id":"rs1800195096","clinical_significance":[]},{"seq_region_name":"7","id":"rs533496019","clinical_significance":[],"strand":1,"feature_type":"variation","end":140619309,"alleles":["T","A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619309,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140619323,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619323,"clinical_significance":[],"id":"rs1800195306","seq_region_name":"7"},{"start":140619324,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140619324,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1053154962","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800195492","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619325,"feature_type":"variation","strand":1,"end":140619325,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs2130717022","clinical_significance":[],"start":140619326,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140619326,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140619330,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619330,"clinical_significance":[],"seq_region_name":"7","id":"rs1800195582"},{"seq_region_name":"7","id":"rs1420024017","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619332,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140619332},{"seq_region_name":"7","id":"rs1800195795","clinical_significance":[],"strand":1,"feature_type":"variation","end":140619335,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619335,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140619337,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619337,"clinical_significance":[],"seq_region_name":"7","id":"rs759764567"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800195979","source":"dbSNP","start":140619338,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140619338,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140619343,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619343,"clinical_significance":[],"seq_region_name":"7","id":"rs931941036"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130717060","source":"dbSNP","start":140619349,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140619349,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619353,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140619353,"clinical_significance":[],"seq_region_name":"7","id":"rs7787017"},{"feature_type":"variation","strand":1,"alleles":["TGATTGCTGA","TGA"],"end":140619362,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619353,"clinical_significance":[],"seq_region_name":"7","id":"rs1183888398"},{"alleles":["G","A"],"end":140619354,"strand":1,"feature_type":"variation","start":140619354,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1800196497","clinical_significance":[]},{"id":"rs1800196610","seq_region_name":"7","clinical_significance":[],"start":140619356,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140619356,"strand":1,"feature_type":"variation"},{"end":140619358,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140619358,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130717078","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619362,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140619362,"clinical_significance":[],"seq_region_name":"7","id":"rs903894438"},{"clinical_significance":[],"id":"rs1399354020","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140619364,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619364},{"end":140619367,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140619367,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130717093","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800196932","feature_type":"variation","strand":1,"end":140619368,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619368},{"seq_region_name":"7","id":"rs1800197037","clinical_significance":[],"alleles":["A","G","T"],"end":140619370,"strand":1,"feature_type":"variation","start":140619370,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619371,"source":"dbSNP","strand":1,"feature_type":"variation","end":140619383,"alleles":["GTGGGTGGGTGGG","GTGGGTGGG"],"seq_region_name":"7","id":"rs1800197118","clinical_significance":[]},{"seq_region_name":"7","id":"rs1800197209","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140619372,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619372,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs376234728","feature_type":"variation","strand":1,"end":140619379,"alleles":["G","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619379},{"feature_type":"variation","strand":1,"end":140619380,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619380,"clinical_significance":[],"seq_region_name":"7","id":"rs1585768764"},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140619385,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619385,"clinical_significance":[],"id":"rs1800197532","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619388,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140619388,"seq_region_name":"7","id":"rs1243857168","clinical_significance":[]},{"seq_region_name":"7","id":"rs999766650","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140619389,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619389,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619392,"source":"dbSNP","strand":1,"feature_type":"variation","end":140619392,"alleles":["G","A"],"seq_region_name":"7","id":"rs1309514232","clinical_significance":[]},{"seq_region_name":"7","id":"rs950149913","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619395,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140619395},{"clinical_significance":[],"seq_region_name":"7","id":"rs1362108909","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619397,"feature_type":"variation","strand":1,"end":140619397,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs2130717138","clinical_significance":[],"end":140619404,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140619404,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs896623701","clinical_significance":[],"start":140619410,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140619410,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130717149","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619413,"feature_type":"variation","strand":1,"end":140619413,"alleles":["G","T"]},{"seq_region_name":"7","id":"rs1397782109","clinical_significance":[],"start":140619414,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140619414,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs184869197","end":140619416,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140619416,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1407318719","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140619420,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619420,"source":"dbSNP"},{"start":140619423,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140619423,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1800198539","clinical_significance":[]},{"alleles":["C","T"],"end":140619424,"feature_type":"variation","strand":1,"source":"dbSNP","start":140619424,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs905883682"},{"seq_region_name":"7","id":"rs544084140","clinical_significance":[],"start":140619427,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140619427,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1326219981","seq_region_name":"7","alleles":["G","A"],"end":140619428,"feature_type":"variation","strand":1,"source":"dbSNP","start":140619428,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1585768870","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140619429,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619429,"source":"dbSNP"},{"clinical_significance":[],"id":"rs7787161","seq_region_name":"7","source":"dbSNP","start":140619432,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C","G"],"end":140619432,"feature_type":"variation","strand":1},{"alleles":["G","A"],"end":140619433,"strand":1,"feature_type":"variation","start":140619433,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1039033688","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619434,"source":"dbSNP","strand":1,"feature_type":"variation","end":140619434,"alleles":["A","G"],"seq_region_name":"7","id":"rs1454690360","clinical_significance":[]},{"id":"rs1800199634","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140619436,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619436,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs898622751","source":"dbSNP","start":140619437,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140619437,"feature_type":"variation","strand":1},{"start":140619442,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140619442,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1800199851","clinical_significance":[]},{"source":"dbSNP","start":140619449,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140619453,"alleles":["TGATG","TG"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585768918"},{"seq_region_name":"7","id":"rs1160942893","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619452,"source":"dbSNP","strand":1,"feature_type":"variation","end":140619452,"alleles":["T","C"]},{"end":140619454,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140619454,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1471365925","clinical_significance":[]},{"seq_region_name":"7","id":"rs1800200240","clinical_significance":[],"start":140619455,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140619455,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1342950464","source":"dbSNP","start":140619458,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140619462,"alleles":["TGATG","TG"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs574571335","clinical_significance":[],"strand":1,"feature_type":"variation","end":140619463,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619463,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1800200555","clinical_significance":[],"alleles":["C","T"],"end":140619468,"strand":1,"feature_type":"variation","start":140619468,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1199448156","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140619475,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619475,"source":"dbSNP"},{"id":"rs1800200740","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619478,"source":"dbSNP","strand":1,"feature_type":"variation","end":140619478,"alleles":["C","A","T"]},{"strand":1,"feature_type":"variation","alleles":["AAA","AA"],"end":140619481,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619479,"source":"dbSNP","id":"rs1800200869","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800200973","alleles":["C","T"],"end":140619484,"feature_type":"variation","strand":1,"source":"dbSNP","start":140619484,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140619484,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["CACTAAAAACTCTGCACTTTTTTTTTTTTTGAGATGGAGTCTCACTCACTCTGTTGCCCAGGCTGGAGTGCAGTGGTGCAATCTCAGCTCACT","CACT"],"end":140619576,"strand":1,"feature_type":"variation","id":"rs1563181861","seq_region_name":"7","clinical_significance":[]},{"end":140619485,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140619485,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1434376322","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1233729568","clinical_significance":[],"alleles":["C","T"],"end":140619486,"strand":1,"feature_type":"variation","start":140619486,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585768979","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140619492,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619492},{"clinical_significance":[],"seq_region_name":"7","id":"rs994292942","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619493,"feature_type":"variation","strand":1,"end":140619493,"alleles":["C","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619496,"feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140619496,"clinical_significance":[],"seq_region_name":"7","id":"rs1027261024"},{"seq_region_name":"7","id":"rs2130717295","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619497,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140619497},{"end":140619499,"alleles":["A","C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140619499,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1269728523"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800201895","feature_type":"variation","strand":1,"end":140619499,"alleles":["A","-"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619499},{"seq_region_name":"7","id":"rs1263961679","clinical_significance":[],"strand":1,"feature_type":"variation","end":140619500,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619500,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585769034","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619501,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140619501},{"alleles":["TTTTTTTTTTTTT","TTTTTTTT","TTTTTTTTTT","TTTTTTTTTTT","TTTTTTTTTTTT","TTTTTTTTTTTTTT","TTTTTTTTTTTTTTT","TTTTTTTTTTTTTTTTT"],"end":140619513,"feature_type":"variation","strand":1,"source":"dbSNP","start":140619501,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs57839820"},{"id":"rs1489372390","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619503,"source":"dbSNP","strand":1,"feature_type":"variation","end":140619503,"alleles":["T","C","G"]},{"seq_region_name":"7","id":"rs1025801654","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619505,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140619505},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619507,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","G"],"end":140619507,"seq_region_name":"7","id":"rs1383210527","clinical_significance":[]},{"seq_region_name":"7","id":"rs955111240","clinical_significance":[],"strand":1,"feature_type":"variation","end":140619513,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619513,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1260709326","alleles":["G","T"],"end":140619514,"feature_type":"variation","strand":1,"source":"dbSNP","start":140619514,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1318905818","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619514,"feature_type":"variation","strand":1,"end":140619514,"alleles":["G","-"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1214752437","source":"dbSNP","start":140619514,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["GAGATGGAG","-"],"end":140619522,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs2130717356","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619515,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140619515},{"start":140619516,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140619516,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1387518389","clinical_significance":[]},{"alleles":["A","C"],"end":140619521,"strand":1,"feature_type":"variation","start":140619521,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130717368","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140619523,"alleles":["T","TTTTTTTTTT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619523,"source":"dbSNP","seq_region_name":"7","id":"rs1451973001","clinical_significance":[]},{"alleles":["T","G"],"end":140619523,"feature_type":"variation","strand":1,"source":"dbSNP","start":140619523,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1800203500"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1176669986","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619524,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140619524},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619525,"source":"dbSNP","strand":1,"feature_type":"variation","end":140619525,"alleles":["T","C"],"seq_region_name":"7","id":"rs2130717388","clinical_significance":[]},{"seq_region_name":"7","id":"rs1800203813","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619530,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140619530},{"clinical_significance":[],"seq_region_name":"7","id":"rs1200911615","source":"dbSNP","start":140619534,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140619534,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1467195092","alleles":["G","C"],"end":140619536,"feature_type":"variation","strand":1,"source":"dbSNP","start":140619536,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800204117","feature_type":"variation","strand":1,"end":140619539,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619539},{"seq_region_name":"7","id":"rs564053703","clinical_significance":[],"start":140619544,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140619544,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140619551,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140619551,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1800204309"},{"clinical_significance":[],"id":"rs2130717430","seq_region_name":"7","end":140619554,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140619554,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800204414","source":"dbSNP","start":140619556,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140619556,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800204492","end":140619559,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140619559,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140619560,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140619560,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130717452"},{"id":"rs1375419161","seq_region_name":"7","clinical_significance":[],"start":140619561,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140619561,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["G","GG"],"end":140619561,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619561,"clinical_significance":[],"seq_region_name":"7","id":"rs2130717464"},{"clinical_significance":[],"seq_region_name":"7","id":"rs983301805","source":"dbSNP","start":140619562,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140619562,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1428982846","source":"dbSNP","start":140619563,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140619563,"alleles":["A","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs541997981","clinical_significance":[],"alleles":["A","T"],"end":140619564,"strand":1,"feature_type":"variation","start":140619564,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["C","A"],"end":140619568,"strand":1,"feature_type":"variation","start":140619568,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs189592899","clinical_significance":[]},{"seq_region_name":"7","id":"rs1007954433","clinical_significance":[],"end":140619569,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140619569,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["G","T"],"end":140619570,"strand":1,"feature_type":"variation","start":140619570,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1375907387","clinical_significance":[]},{"seq_region_name":"7","id":"rs1800205328","clinical_significance":[],"alleles":["C","G"],"end":140619571,"strand":1,"feature_type":"variation","start":140619571,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1800205437","seq_region_name":"7","end":140619575,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140619575,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1800205530","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619576,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140619576},{"start":140619578,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140619578,"alleles":["C","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs944496762","clinical_significance":[]},{"end":140619580,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140619580,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1585769209","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1202378095","alleles":["C","A"],"end":140619581,"feature_type":"variation","strand":1,"source":"dbSNP","start":140619581,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140619584,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140619584,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1342978352","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1255418627","source":"dbSNP","start":140619585,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140619585,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1228829918","feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140619586,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619586},{"clinical_significance":[],"id":"rs1800206327","seq_region_name":"7","end":140619594,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140619594,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","A","T"],"end":140619598,"feature_type":"variation","strand":1,"source":"dbSNP","start":140619598,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1017916853"},{"seq_region_name":"7","id":"rs566812505","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619599,"source":"dbSNP","strand":1,"feature_type":"variation","end":140619599,"alleles":["G","A","C"]},{"clinical_significance":[],"id":"rs534056441","seq_region_name":"7","source":"dbSNP","start":140619602,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140619602,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs979340136","source":"dbSNP","start":140619603,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140619603,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs925194123","clinical_significance":[],"alleles":["A","G"],"end":140619604,"strand":1,"feature_type":"variation","start":140619604,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140619612,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619612,"clinical_significance":[],"seq_region_name":"7","id":"rs1800206962"},{"id":"rs1383984557","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619616,"source":"dbSNP","strand":1,"feature_type":"variation","end":140619616,"alleles":["C","G"]},{"seq_region_name":"7","id":"rs1337052587","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619619,"source":"dbSNP","strand":1,"feature_type":"variation","end":140619619,"alleles":["C","A","T"]},{"id":"rs1397362098","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140619620,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619620,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1417415324","clinical_significance":[],"start":140619622,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140619622,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800207500","source":"dbSNP","start":140619625,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140619625,"alleles":["A","T"],"feature_type":"variation","strand":1},{"end":140619628,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140619628,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs527707599","clinical_significance":[]},{"seq_region_name":"7","id":"rs921794851","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619637,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140619637},{"clinical_significance":[],"id":"rs1800207802","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619644,"feature_type":"variation","strand":1,"end":140619644,"alleles":["C","T"]},{"end":140619645,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140619645,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs546186337","clinical_significance":[]},{"end":140619647,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140619647,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs564459334"},{"source":"dbSNP","start":140619648,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140619648,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs532074077","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1043856090","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619650,"source":"dbSNP","strand":1,"feature_type":"variation","end":140619650,"alleles":["C","A","T"]},{"alleles":["C","A","G"],"end":140619651,"strand":1,"feature_type":"variation","start":140619651,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1243462238","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619652,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140619652,"id":"rs1800208776","seq_region_name":"7","clinical_significance":[]},{"start":140619653,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140619653,"alleles":["C","T"],"strand":1,"feature_type":"variation","id":"rs1189883630","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1800208982","clinical_significance":[],"end":140619655,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140619655,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1440868906","clinical_significance":[],"alleles":["A","G"],"end":140619661,"strand":1,"feature_type":"variation","start":140619661,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs917786376","end":140619665,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140619665,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["T","C"],"end":140619670,"strand":1,"feature_type":"variation","start":140619670,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs765040027","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800209435","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619671,"feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140619671},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800209540","source":"dbSNP","start":140619672,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140619672,"alleles":["G","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800209651","feature_type":"variation","strand":1,"end":140619679,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619679},{"seq_region_name":"7","id":"rs1800209753","clinical_significance":[],"strand":1,"feature_type":"variation","end":140619681,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619681,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140619686,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619686,"source":"dbSNP","seq_region_name":"7","id":"rs1196509845","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1484060354","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140619687,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619687},{"seq_region_name":"7","id":"rs1273190512","clinical_significance":[],"start":140619688,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140619688,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619694,"feature_type":"variation","strand":1,"end":140619694,"alleles":["T","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1800210178"},{"id":"rs1228295899","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140619696,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619696,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1046243872","feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140619697,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619697},{"source":"dbSNP","start":140619699,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140619699,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs2130717705","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130717709","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619700,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140619700},{"start":140619704,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140619704,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1800210524","clinical_significance":[]},{"alleles":["A","G"],"end":140619709,"feature_type":"variation","strand":1,"source":"dbSNP","start":140619709,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1369485878","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619710,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140619710,"clinical_significance":[],"seq_region_name":"7","id":"rs1286255407"},{"seq_region_name":"7","id":"rs2130717735","clinical_significance":[],"strand":1,"feature_type":"variation","end":140619712,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619712,"source":"dbSNP"},{"alleles":["C","G"],"end":140619715,"strand":1,"feature_type":"variation","start":140619715,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1800210946","clinical_significance":[]},{"alleles":["T","C"],"end":140619719,"strand":1,"feature_type":"variation","start":140619719,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs2130717750","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585769470","feature_type":"variation","strand":1,"alleles":["A","C","T"],"end":140619722,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619722},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130717770","alleles":["T","C"],"end":140619724,"feature_type":"variation","strand":1,"source":"dbSNP","start":140619724,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1800211137","seq_region_name":"7","alleles":["C","T"],"end":140619725,"feature_type":"variation","strand":1,"source":"dbSNP","start":140619725,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140619726,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140619726,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs927280739"},{"alleles":["C","T"],"end":140619730,"strand":1,"feature_type":"variation","start":140619730,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1585769490","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800211495","feature_type":"variation","strand":1,"end":140619731,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619731},{"source":"dbSNP","start":140619732,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140619732,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1310015228"},{"seq_region_name":"7","id":"rs1333055754","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619733,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140619733},{"seq_region_name":"7","id":"rs1355963896","clinical_significance":[],"alleles":["A","G"],"end":140619734,"strand":1,"feature_type":"variation","start":140619734,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs2130717805","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["AA","-"],"end":140619735,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619734,"source":"dbSNP"},{"seq_region_name":"7","id":"rs937339704","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140619737,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619737,"source":"dbSNP"},{"seq_region_name":"7","id":"rs896743820","clinical_significance":[],"start":140619738,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C","T"],"end":140619738,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1800212511","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["ATCT","ATCTATCT"],"end":140619742,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619739,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1371853219","seq_region_name":"7","source":"dbSNP","start":140619741,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140619741,"feature_type":"variation","strand":1},{"alleles":["C","A","T"],"end":140619744,"feature_type":"variation","strand":1,"source":"dbSNP","start":140619744,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1038409373"},{"feature_type":"variation","strand":1,"end":140619748,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619748,"clinical_significance":[],"seq_region_name":"7","id":"rs550494659"},{"clinical_significance":[],"id":"rs377383960","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140619749,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619749},{"source":"dbSNP","start":140619751,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140619751,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1356760483"},{"id":"rs898735336","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619752,"source":"dbSNP","strand":1,"feature_type":"variation","end":140619752,"alleles":["G","A","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619753,"source":"dbSNP","strand":1,"feature_type":"variation","end":140619753,"alleles":["G","A"],"seq_region_name":"7","id":"rs1265038124","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140619759,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619759,"clinical_significance":[],"seq_region_name":"7","id":"rs1800213798"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800213924","source":"dbSNP","start":140619762,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140619762,"alleles":["A","T"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619763,"source":"dbSNP","strand":1,"feature_type":"variation","end":140619763,"alleles":["G","A"],"seq_region_name":"7","id":"rs2130717878","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585769588","alleles":["G","C"],"end":140619765,"feature_type":"variation","strand":1,"source":"dbSNP","start":140619765,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140619768,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140619768,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs568603679"},{"seq_region_name":"7","id":"rs1182794576","clinical_significance":[],"strand":1,"feature_type":"variation","end":140619772,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619772,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140619780,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619780,"clinical_significance":[],"id":"rs529451693","seq_region_name":"7"},{"start":140619782,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140619782,"alleles":["G","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1249641271","clinical_significance":[]},{"seq_region_name":"7","id":"rs547980104","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619787,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140619787},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585769641","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140619792,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619792},{"seq_region_name":"7","id":"rs1001229070","clinical_significance":[],"end":140619794,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140619794,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs2130717927","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619795,"source":"dbSNP","strand":1,"feature_type":"variation","end":140619795,"alleles":["C","G"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619798,"feature_type":"variation","strand":1,"end":140619798,"alleles":["C","A"],"clinical_significance":[],"id":"rs1800214731","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1179191776","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140619804,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619804,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1490645610","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140619809,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619809,"source":"dbSNP"},{"start":140619811,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140619811,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1800215039","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619815,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140619815,"clinical_significance":[],"seq_region_name":"7","id":"rs2130717949"},{"feature_type":"variation","strand":1,"end":140619818,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619818,"clinical_significance":[],"seq_region_name":"7","id":"rs1047199048"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800215242","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619820,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140619820},{"seq_region_name":"7","id":"rs1800215338","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619824,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140619824},{"clinical_significance":[],"seq_region_name":"7","id":"rs1292501589","end":140619828,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140619828,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800215581","source":"dbSNP","start":140619836,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140619836,"alleles":["T","C"],"feature_type":"variation","strand":1},{"id":"rs1800215671","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619842,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140619842},{"end":140619849,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140619849,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1208483397","seq_region_name":"7","clinical_significance":[]},{"start":140619852,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140619852,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1800215865","clinical_significance":[]},{"end":140619855,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140619855,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1356081692","clinical_significance":[]},{"id":"rs1283292208","seq_region_name":"7","clinical_significance":[],"alleles":["A","G"],"end":140619859,"strand":1,"feature_type":"variation","start":140619859,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619860,"source":"dbSNP","strand":1,"feature_type":"variation","end":140619860,"alleles":["T","C"],"id":"rs1585769696","seq_region_name":"7","clinical_significance":[]},{"id":"rs1800216227","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619864,"source":"dbSNP","strand":1,"feature_type":"variation","end":140619864,"alleles":["A","G"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619865,"source":"dbSNP","strand":1,"feature_type":"variation","end":140619865,"alleles":["T","C"],"seq_region_name":"7","id":"rs891311240","clinical_significance":[]},{"source":"dbSNP","start":140619866,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140619866,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1239396938"},{"clinical_significance":[],"id":"rs566530844","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140619868,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619868},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585769738","source":"dbSNP","start":140619872,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140619872,"alleles":["T","G"],"feature_type":"variation","strand":1},{"end":140619875,"alleles":["A","C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140619875,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1007905251","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["CTCA","-"],"end":140619880,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619877,"clinical_significance":[],"seq_region_name":"7","id":"rs1800216701"},{"id":"rs1018450058","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140619882,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619882,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140619883,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619883,"source":"dbSNP","id":"rs1368737781","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140619886,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619886,"clinical_significance":[],"id":"rs781048155","seq_region_name":"7"},{"alleles":["A","G"],"end":140619889,"feature_type":"variation","strand":1,"source":"dbSNP","start":140619889,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1800217096"},{"clinical_significance":[],"id":"rs180780796","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619902,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140619902},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800217189","source":"dbSNP","start":140619905,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140619905,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1000936937","clinical_significance":[],"end":140619906,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140619906,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140619913,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140619913,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs374629033"},{"strand":1,"feature_type":"variation","end":140619917,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619917,"source":"dbSNP","seq_region_name":"7","id":"rs1800217438","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1004505681","alleles":["C","T"],"end":140619920,"feature_type":"variation","strand":1,"source":"dbSNP","start":140619920,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619922,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140619922,"clinical_significance":[],"id":"rs1800217622","seq_region_name":"7"},{"start":140619928,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140619928,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1403463615","clinical_significance":[]},{"end":140619930,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140619930,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1389735161","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1032044015","feature_type":"variation","strand":1,"end":140619931,"alleles":["G","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619931},{"strand":1,"feature_type":"variation","end":140619932,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619932,"source":"dbSNP","id":"rs1473659061","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1409893050","end":140619933,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140619933,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs956598373","source":"dbSNP","start":140619934,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140619934,"alleles":["T","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs965981837","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619937,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AA","AAA"],"end":140619938},{"clinical_significance":[],"seq_region_name":"7","id":"rs988082928","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619939,"feature_type":"variation","strand":1,"end":140619939,"alleles":["C","G","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs976442326","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619945,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140619945},{"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140619947,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619947,"clinical_significance":[],"seq_region_name":"7","id":"rs1800218663"},{"seq_region_name":"7","id":"rs1800218747","clinical_significance":[],"alleles":["T","C"],"end":140619949,"strand":1,"feature_type":"variation","start":140619949,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619950,"feature_type":"variation","strand":1,"end":140619950,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1440743586"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619951,"source":"dbSNP","strand":1,"feature_type":"variation","end":140619951,"alleles":["G","C"],"seq_region_name":"7","id":"rs1249032220","clinical_significance":[]},{"seq_region_name":"7","id":"rs1800219034","clinical_significance":[],"alleles":["A","G"],"end":140619953,"strand":1,"feature_type":"variation","start":140619953,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140619957,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140619957,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1800219118","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs185199643","source":"dbSNP","start":140619959,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140619959,"alleles":["A","G"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140619962,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619962,"source":"dbSNP","id":"rs189232131","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1389806189","seq_region_name":"7","feature_type":"variation","strand":1,"end":140619963,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619963},{"end":140619965,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140619965,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs537794234"},{"alleles":["G","A"],"end":140619968,"strand":1,"feature_type":"variation","start":140619968,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1800219620","clinical_significance":[]},{"start":140619970,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140619970,"alleles":["A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1800219717","clinical_significance":[]},{"seq_region_name":"7","id":"rs1800219808","clinical_significance":[],"end":140619975,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140619975,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800219905","alleles":["T","C","G"],"end":140619976,"feature_type":"variation","strand":1,"source":"dbSNP","start":140619976,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140619982,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140619982,"clinical_significance":[],"seq_region_name":"7","id":"rs970554785"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800220120","source":"dbSNP","start":140619983,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140619983,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800220207","source":"dbSNP","start":140619984,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140619984,"alleles":["G","A"],"feature_type":"variation","strand":1},{"id":"rs981507811","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619986,"source":"dbSNP","strand":1,"feature_type":"variation","end":140619986,"alleles":["A","G"]},{"start":140619987,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140619987,"strand":1,"feature_type":"variation","id":"rs1800220420","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1227289463","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140619991,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140619991},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800220632","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620004,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140620004},{"seq_region_name":"7","id":"rs370682563","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140620005,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620005,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1563182161","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620006,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140620006},{"seq_region_name":"7","id":"rs937473455","clinical_significance":[],"end":140620018,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140620018,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs768669644","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620021,"feature_type":"variation","strand":1,"end":140620021,"alleles":["C","G","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs556413115","feature_type":"variation","strand":1,"end":140620022,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620022},{"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140620027,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620027,"clinical_significance":[],"seq_region_name":"7","id":"rs573783241"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620040,"source":"dbSNP","strand":1,"feature_type":"variation","end":140620046,"alleles":["AAAAAAA","AAAAAAAA","AAAAAAAAA"],"seq_region_name":"7","id":"rs111793348","clinical_significance":[]},{"seq_region_name":"7","id":"rs1386795224","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620042,"source":"dbSNP","strand":1,"feature_type":"variation","end":140620042,"alleles":["A","G"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620046,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140620046,"seq_region_name":"7","id":"rs1800222978","clinical_significance":[]},{"source":"dbSNP","start":140620047,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140620047,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1800223095"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1047315907","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140620048,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620048},{"seq_region_name":"7","id":"rs1800223309","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620050,"source":"dbSNP","strand":1,"feature_type":"variation","end":140620050,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs891260692","clinical_significance":[],"end":140620051,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140620051,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1415166739","feature_type":"variation","strand":1,"end":140620052,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620052},{"feature_type":"variation","strand":1,"end":140620053,"alleles":["G","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620053,"clinical_significance":[],"seq_region_name":"7","id":"rs1199185540"},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140620056,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620056,"clinical_significance":[],"seq_region_name":"7","id":"rs1189984697"},{"end":140620060,"alleles":["G","A","C","T"],"strand":1,"feature_type":"variation","start":140620060,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1800223732","clinical_significance":[]},{"seq_region_name":"7","id":"rs1477964063","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140620063,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620063,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1585770080","clinical_significance":[],"end":140620064,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140620064,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140620065,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620065,"source":"dbSNP","id":"rs761762543","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1039912347","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140620066,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620066},{"feature_type":"variation","strand":1,"end":140620067,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620067,"clinical_significance":[],"seq_region_name":"7","id":"rs1712092073"},{"source":"dbSNP","start":140620068,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140620068,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1190960482"},{"clinical_significance":[],"seq_region_name":"7","id":"rs899575736","source":"dbSNP","start":140620069,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C","T"],"end":140620069,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1585770135","clinical_significance":[],"start":140620072,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140620072,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140620075,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140620075,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1312281436"},{"start":140620076,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140620076,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1000651341","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585770161","feature_type":"variation","strand":1,"end":140620077,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620077},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620082,"feature_type":"variation","strand":1,"end":140620082,"alleles":["A","G"],"clinical_significance":[],"id":"rs1800224988","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs949644241","end":140620085,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140620085,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140620087,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140620087,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1800225173","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620088,"source":"dbSNP","strand":1,"feature_type":"variation","end":140620088,"alleles":["C","G"],"seq_region_name":"7","id":"rs1045758180","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140620089,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620089,"source":"dbSNP","seq_region_name":"7","id":"rs1800225400","clinical_significance":[]},{"end":140620097,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140620097,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1256289572","clinical_significance":[]},{"start":140620100,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140620100,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs868593217","clinical_significance":[]},{"start":140620104,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140620104,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1800225713","clinical_significance":[]},{"source":"dbSNP","start":140620105,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140620105,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585770193"},{"seq_region_name":"7","id":"rs1437064784","clinical_significance":[],"start":140620106,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140620106,"strand":1,"feature_type":"variation"},{"alleles":["T","A"],"end":140620109,"strand":1,"feature_type":"variation","start":140620109,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585770208","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1032407526","source":"dbSNP","start":140620110,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140620110,"alleles":["C","T"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140620111,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620111,"source":"dbSNP","seq_region_name":"7","id":"rs1320153123","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620112,"source":"dbSNP","strand":1,"feature_type":"variation","end":140620112,"alleles":["C","T"],"seq_region_name":"7","id":"rs892156304","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140620114,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620114,"source":"dbSNP","seq_region_name":"7","id":"rs1360996181","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140620116,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620116,"clinical_significance":[],"seq_region_name":"7","id":"rs1009452105"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1184984218","end":140620117,"alleles":["AA","AAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140620116,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140620118,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140620118,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1413955244"},{"alleles":["A","C","G"],"end":140620121,"strand":1,"feature_type":"variation","start":140620121,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1024898655","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800226808","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620122,"feature_type":"variation","strand":1,"end":140620122,"alleles":["G","C"]},{"end":140620124,"alleles":["A","C","G"],"strand":1,"feature_type":"variation","start":140620124,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs544434448","seq_region_name":"7","clinical_significance":[]},{"start":140620126,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140620126,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1048758337","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs981003246","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140620127,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620127},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620128,"feature_type":"variation","strand":1,"end":140620128,"alleles":["G","A"],"clinical_significance":[],"id":"rs367629203","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1800227352","clinical_significance":[],"start":140620131,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140620131,"strand":1,"feature_type":"variation"},{"start":140620133,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140620133,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585770336","clinical_significance":[]},{"source":"dbSNP","start":140620135,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140620135,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1454057982"},{"alleles":["GCATGGAGC","GC"],"end":140620143,"strand":1,"feature_type":"variation","start":140620135,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1460946412","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1238727615","source":"dbSNP","start":140620137,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140620137,"alleles":["A","C","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1297631941","source":"dbSNP","start":140620138,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140620138,"feature_type":"variation","strand":1},{"start":140620139,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140620139,"alleles":["G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1403015940","clinical_significance":[]},{"id":"rs1397934221","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140620140,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620140,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1306489486","end":140620149,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140620149,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800228243","feature_type":"variation","strand":1,"end":140620150,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620150},{"strand":1,"feature_type":"variation","end":140620152,"alleles":["C","A","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620152,"source":"dbSNP","seq_region_name":"7","id":"rs959024392","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140620153,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620153,"clinical_significance":[],"seq_region_name":"7","id":"rs1354564723"},{"alleles":["A","G"],"end":140620156,"feature_type":"variation","strand":1,"source":"dbSNP","start":140620156,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs887534484","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130718593","source":"dbSNP","start":140620158,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140620158,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1381680333","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620161,"feature_type":"variation","strand":1,"end":140620161,"alleles":["A","C","G"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620162,"feature_type":"variation","strand":1,"end":140620162,"alleles":["C","G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1301284544"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140620163,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620163,"source":"dbSNP","id":"rs974202389","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620164,"source":"dbSNP","strand":1,"feature_type":"variation","end":140620164,"alleles":["C","G"],"seq_region_name":"7","id":"rs1800228921","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1447476826","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140620165,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620165},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620169,"feature_type":"variation","strand":1,"end":140620169,"alleles":["C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1800229110"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620170,"feature_type":"variation","strand":1,"end":140620170,"alleles":["T","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs919897791"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585770468","feature_type":"variation","strand":1,"end":140620172,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620172},{"clinical_significance":[],"seq_region_name":"7","id":"rs780009068","feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140620174,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620174},{"clinical_significance":[],"id":"rs1014588645","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620175,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140620175},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620177,"source":"dbSNP","strand":1,"feature_type":"variation","end":140620177,"alleles":["C","T"],"seq_region_name":"7","id":"rs2130718654","clinical_significance":[]},{"end":140620178,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140620178,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1800229670"},{"seq_region_name":"7","id":"rs1389982340","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620181,"source":"dbSNP","strand":1,"feature_type":"variation","end":140620181,"alleles":["G","A"]},{"source":"dbSNP","start":140620181,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140620181,"alleles":["G","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1800229858"},{"seq_region_name":"7","id":"rs1428309434","clinical_significance":[],"start":140620181,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["GTAAGACTCTG","-"],"end":140620191,"strand":1,"feature_type":"variation"},{"end":140620182,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140620182,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1585770507","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1305658275","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620183,"source":"dbSNP","strand":1,"feature_type":"variation","end":140620183,"alleles":["A","G"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620187,"feature_type":"variation","strand":1,"end":140620187,"alleles":["C","G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs982958218"},{"seq_region_name":"7","id":"rs1800230418","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620187,"source":"dbSNP","strand":1,"feature_type":"variation","end":140620190,"alleles":["CTCT","CT"]},{"seq_region_name":"7","id":"rs1585770541","clinical_significance":[],"start":140620190,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140620190,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585770553","feature_type":"variation","strand":1,"end":140620191,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620191},{"source":"dbSNP","start":140620194,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140620194,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs2130718693","seq_region_name":"7"},{"alleles":["C","A"],"end":140620195,"strand":1,"feature_type":"variation","start":140620195,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1425905474","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563182348","feature_type":"variation","strand":1,"end":140620202,"alleles":["AAAAAAA","AAAAAA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620196},{"seq_region_name":"7","id":"rs1800230930","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140620200,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620200,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800231035","feature_type":"variation","strand":1,"end":140620202,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620202},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620203,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140620203,"seq_region_name":"7","id":"rs1585770581","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1415566024","end":140620204,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140620204,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1800231336","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620204,"source":"dbSNP","strand":1,"feature_type":"variation","end":140620210,"alleles":["AAAAAAA","AAAAAA"]},{"id":"rs1800231443","seq_region_name":"7","clinical_significance":[],"start":140620211,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","GG"],"end":140620211,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620217,"feature_type":"variation","strand":1,"end":140620217,"alleles":["T","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1179755402"},{"seq_region_name":"7","id":"rs1800231762","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140620221,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620221,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1800231930","seq_region_name":"7","alleles":["A","T"],"end":140620222,"feature_type":"variation","strand":1,"source":"dbSNP","start":140620222,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140620223,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140620223,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1203763645"},{"source":"dbSNP","start":140620227,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140620227,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1474600327"},{"seq_region_name":"7","id":"rs751242138","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620228,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140620228},{"seq_region_name":"7","id":"rs1256016976","clinical_significance":[],"strand":1,"feature_type":"variation","end":140620230,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620230,"source":"dbSNP"},{"end":140620231,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140620231,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1800232775"},{"start":140620232,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140620232,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs553990785","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140620233,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620233,"clinical_significance":[],"seq_region_name":"7","id":"rs944337850"},{"id":"rs1800233253","seq_region_name":"7","clinical_significance":[],"start":140620236,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140620236,"strand":1,"feature_type":"variation"},{"alleles":["A","G"],"end":140620239,"strand":1,"feature_type":"variation","start":140620239,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1800233377","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["AAGAAGA","AAGA"],"end":140620247,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620241,"source":"dbSNP","seq_region_name":"7","id":"rs1207245552","clinical_significance":[]},{"seq_region_name":"7","id":"rs1800233577","clinical_significance":[],"start":140620243,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140620243,"alleles":["G","-"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1482003077","end":140620244,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140620244,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1800233770","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620245,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140620245},{"seq_region_name":"7","id":"rs1800233858","clinical_significance":[],"end":140620246,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140620246,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140620247,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140620247,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1250668160"},{"end":140620250,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140620250,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130718817"},{"seq_region_name":"7","id":"rs1800234019","clinical_significance":[],"alleles":["T","C"],"end":140620251,"strand":1,"feature_type":"variation","start":140620251,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800234109","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140620252,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620252},{"start":140620255,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C","G"],"end":140620255,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1222080460","clinical_significance":[]},{"seq_region_name":"7","id":"rs1323280224","clinical_significance":[],"strand":1,"feature_type":"variation","end":140620258,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620258,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140620261,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620261,"clinical_significance":[],"seq_region_name":"7","id":"rs1800234455"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620262,"feature_type":"variation","strand":1,"end":140620267,"alleles":["AAAAAA","AAAAA","AAAAAAA"],"clinical_significance":[],"seq_region_name":"7","id":"rs1310919521"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620268,"feature_type":"variation","strand":1,"end":140620268,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1585770700"},{"seq_region_name":"7","id":"rs2130718848","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620268,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","-"],"end":140620268},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620269,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140620269,"clinical_significance":[],"seq_region_name":"7","id":"rs1227899686"},{"seq_region_name":"7","id":"rs1040265062","clinical_significance":[],"strand":1,"feature_type":"variation","end":140620271,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620271,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140620272,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620272,"clinical_significance":[],"seq_region_name":"7","id":"rs900023883"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1198369446","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620276,"feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140620276},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620281,"feature_type":"variation","strand":1,"end":140620281,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1800235240"},{"id":"rs1800235349","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620282,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140620282},{"start":140620285,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140620285,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs966124724","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140620289,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620289,"clinical_significance":[],"seq_region_name":"7","id":"rs1800235547"},{"source":"dbSNP","start":140620294,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140620294,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1800235646","seq_region_name":"7"},{"id":"rs997429105","seq_region_name":"7","clinical_significance":[],"alleles":["A","G"],"end":140620297,"strand":1,"feature_type":"variation","start":140620297,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620298,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140620298,"clinical_significance":[],"seq_region_name":"7","id":"rs1800235828"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620299,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140620299,"clinical_significance":[],"seq_region_name":"7","id":"rs1459832837"},{"start":140620300,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140620300,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1348490080","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140620304,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620304,"clinical_significance":[],"seq_region_name":"7","id":"rs1800236147"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1162258776","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620310,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140620310},{"seq_region_name":"7","id":"rs1800236371","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620313,"source":"dbSNP","strand":1,"feature_type":"variation","end":140620313,"alleles":["T","G"]},{"seq_region_name":"7","id":"rs1800236452","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620314,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140620314},{"seq_region_name":"7","id":"rs1800236548","clinical_significance":[],"end":140620319,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140620319,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800236650","source":"dbSNP","start":140620320,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AAAA","AAA"],"end":140620323,"feature_type":"variation","strand":1},{"id":"rs936395433","seq_region_name":"7","clinical_significance":[],"start":140620321,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140620321,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140620325,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140620325,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1800236841"},{"seq_region_name":"7","id":"rs1800236948","clinical_significance":[],"start":140620326,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140620326,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"id":"rs1800237041","seq_region_name":"7","clinical_significance":[],"start":140620337,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140620337,"strand":1,"feature_type":"variation"},{"start":140620338,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140620338,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1800237143","clinical_significance":[]},{"source":"dbSNP","start":140620338,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TTT","TT"],"end":140620340,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1800237245"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1460553770","end":140620340,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140620340,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1412090535","source":"dbSNP","start":140620344,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140620344,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140620345,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140620345,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1800237521"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1475072954","source":"dbSNP","start":140620345,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140620348,"alleles":["GGGG","GGG"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140620346,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140620346,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1029344500"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620348,"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140620348,"clinical_significance":[],"seq_region_name":"7","id":"rs1800237821"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800237908","end":140620350,"alleles":["GTG","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140620348,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs141931145","alleles":["T","-"],"end":140620349,"feature_type":"variation","strand":1,"source":"dbSNP","start":140620349,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs200792200","clinical_significance":[],"alleles":["T","A","G"],"end":140620349,"strand":1,"feature_type":"variation","start":140620349,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["T","TT"],"end":140620349,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620349,"source":"dbSNP","seq_region_name":"7","id":"rs1800238128","clinical_significance":[]},{"id":"rs1800238321","seq_region_name":"7","clinical_significance":[],"end":140620349,"alleles":["-","C"],"strand":1,"feature_type":"variation","start":140620350,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["G","A","C","T"],"end":140620350,"feature_type":"variation","strand":1,"source":"dbSNP","start":140620350,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs572607294"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620350,"feature_type":"variation","strand":1,"end":140620359,"alleles":["GGGGGGGGGG","GGGGGGGG","GGGGGGGGG","GGGGGGGGGGG","GGGGGGGGGGGG"],"clinical_significance":[],"seq_region_name":"7","id":"rs10708233"},{"end":140620350,"alleles":["-","C"],"strand":1,"feature_type":"variation","start":140620351,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1491380999","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620351,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140620351,"clinical_significance":[],"id":"rs892095653","seq_region_name":"7"},{"source":"dbSNP","start":140620352,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140620351,"alleles":["-","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1349949387"},{"alleles":["G","A","C","T"],"end":140620352,"strand":1,"feature_type":"variation","start":140620352,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1009232901","clinical_significance":[]},{"id":"rs546298791","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140620353,"alleles":["G","A","C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620353,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140620354,"alleles":["G","A","C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620354,"clinical_significance":[],"seq_region_name":"7","id":"rs906427856"},{"start":140620355,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["-","T"],"end":140620354,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1800239672","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620355,"feature_type":"variation","strand":1,"alleles":["G","A","C","T"],"end":140620355,"clinical_significance":[],"seq_region_name":"7","id":"rs917914935"},{"alleles":["-","C"],"end":140620355,"feature_type":"variation","strand":1,"source":"dbSNP","start":140620356,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1176711155"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1400878197","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620356,"feature_type":"variation","strand":1,"end":140620356,"alleles":["G","A","C"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620357,"source":"dbSNP","strand":1,"feature_type":"variation","end":140620357,"alleles":["G","A"],"seq_region_name":"7","id":"rs556338450","clinical_significance":[]},{"seq_region_name":"7","id":"rs1800240407","clinical_significance":[],"start":140620358,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140620358,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1800240561","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620358,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["GGAGGAGGA","GGAGGA"],"end":140620366},{"id":"rs1465158123","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620359,"source":"dbSNP","strand":1,"feature_type":"variation","end":140620359,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs934584304","clinical_significance":[],"start":140620360,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140620360,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1250211189","seq_region_name":"7","source":"dbSNP","start":140620360,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140620360,"alleles":["A","-"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1350067358","feature_type":"variation","strand":1,"alleles":["A","G"],"end":140620363,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620363},{"seq_region_name":"7","id":"rs1585770973","clinical_significance":[],"strand":1,"feature_type":"variation","end":140620366,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620366,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1359624645","clinical_significance":[],"end":140620369,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140620369,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1800241694","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620373,"source":"dbSNP","strand":1,"feature_type":"variation","end":140620373,"alleles":["T","C"]},{"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140620376,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620376,"clinical_significance":[],"seq_region_name":"7","id":"rs1256619530"},{"start":140620379,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140620379,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1236093456","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585770997","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140620386,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620386,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140620389,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620389,"source":"dbSNP","id":"rs1311003442","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1800242504","clinical_significance":[],"start":140620392,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140620392,"strand":1,"feature_type":"variation"},{"id":"rs949429399","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140620393,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620393,"source":"dbSNP"},{"id":"rs1800242827","seq_region_name":"7","clinical_significance":[],"alleles":["AAAA","AAA"],"end":140620396,"strand":1,"feature_type":"variation","start":140620393,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620400,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140620400,"seq_region_name":"7","id":"rs1436362946","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620402,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140620402,"seq_region_name":"7","id":"rs1002149556","clinical_significance":[]},{"end":140620403,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140620403,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1322151573"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1432355922","feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140620404,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620404},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140620408,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620408,"source":"dbSNP","seq_region_name":"7","id":"rs1800243688","clinical_significance":[]},{"end":140620414,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140620414,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1045295600"},{"end":140620419,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140620419,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1800244031","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140620425,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620425,"clinical_significance":[],"seq_region_name":"7","id":"rs1800244204"},{"source":"dbSNP","start":140620426,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140620426,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1467113243"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620436,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140620436,"clinical_significance":[],"id":"rs1800244522","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1375900125","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620438,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140620438},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620440,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140620440,"seq_region_name":"7","id":"rs1313426568","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620442,"source":"dbSNP","strand":1,"feature_type":"variation","end":140620442,"alleles":["C","T"],"seq_region_name":"7","id":"rs1033906497","clinical_significance":[]},{"clinical_significance":[],"id":"rs181120636","seq_region_name":"7","source":"dbSNP","start":140620443,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C","G"],"end":140620443,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800245076","source":"dbSNP","start":140620444,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140620444,"alleles":["T","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs926877894","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620446,"feature_type":"variation","strand":1,"alleles":["GGG","GG"],"end":140620448},{"id":"rs1446586555","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620451,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140620451},{"clinical_significance":[],"seq_region_name":"7","id":"rs1257092630","end":140620459,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140620459,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1800245499","clinical_significance":[],"alleles":["T","TCT"],"end":140620459,"strand":1,"feature_type":"variation","start":140620459,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["G","A"],"end":140620460,"feature_type":"variation","strand":1,"source":"dbSNP","start":140620460,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1800245597"},{"seq_region_name":"7","id":"rs931445706","clinical_significance":[],"alleles":["A","AA"],"end":140620461,"strand":1,"feature_type":"variation","start":140620461,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140620471,"alleles":["TTTTTTTTTT","TTTTTTTTT","TTTTTTTTTTT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620462,"clinical_significance":[],"seq_region_name":"7","id":"rs887315214"},{"end":140620463,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140620463,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1747307921"},{"source":"dbSNP","start":140620472,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140620472,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1488385423","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140620473,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620473,"clinical_significance":[],"seq_region_name":"7","id":"rs1218354741"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1265708914","end":140620474,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140620474,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","A","T"],"end":140620477,"strand":1,"feature_type":"variation","start":140620477,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1485134129","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620479,"feature_type":"variation","strand":1,"end":140620479,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1186429048"},{"alleles":["C","T"],"end":140620483,"strand":1,"feature_type":"variation","start":140620483,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1426540392","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs373233156","clinical_significance":[],"alleles":["T","C"],"end":140620489,"strand":1,"feature_type":"variation","start":140620489,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140620496,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140620504,"alleles":["AACAACAAC","AACAAC"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1224816326"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620499,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140620499,"id":"rs1800246732","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1325542103","source":"dbSNP","start":140620502,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140620502,"alleles":["A","C"],"feature_type":"variation","strand":1},{"alleles":["A","G"],"end":140620503,"strand":1,"feature_type":"variation","start":140620503,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1036549953","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800247005","feature_type":"variation","strand":1,"end":140620507,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620507},{"source":"dbSNP","start":140620507,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140620513,"alleles":["CCCCCCC","CCCCCC","CCCCCCCC"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1397340221"},{"clinical_significance":[],"id":"rs1312218190","seq_region_name":"7","alleles":["C","T"],"end":140620508,"feature_type":"variation","strand":1,"source":"dbSNP","start":140620508,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1430260500","seq_region_name":"7","source":"dbSNP","start":140620509,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140620509,"feature_type":"variation","strand":1},{"start":140620511,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140620511,"alleles":["C","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1800247508","clinical_significance":[]},{"seq_region_name":"7","id":"rs79484224","clinical_significance":[],"end":140620513,"alleles":["C","A","G","T"],"strand":1,"feature_type":"variation","start":140620513,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1166531762","seq_region_name":"7","clinical_significance":[],"start":140620514,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140620514,"alleles":["A","AA"],"strand":1,"feature_type":"variation"},{"alleles":["C","A","T"],"end":140620515,"strand":1,"feature_type":"variation","start":140620515,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1027030934","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1800247997","clinical_significance":[],"start":140620517,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140620517,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1394584883","alleles":["G","A"],"end":140620518,"feature_type":"variation","strand":1,"source":"dbSNP","start":140620518,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140620519,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140620519,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1800248297","clinical_significance":[]},{"clinical_significance":[],"id":"rs889029845","seq_region_name":"7","source":"dbSNP","start":140620532,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140620532,"alleles":["C","G"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140620533,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620533,"source":"dbSNP","seq_region_name":"7","id":"rs544139463","clinical_significance":[]},{"source":"dbSNP","start":140620534,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140620534,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1206540959","seq_region_name":"7"},{"id":"rs1800248890","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140620536,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620536,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800249045","alleles":["A","G"],"end":140620537,"feature_type":"variation","strand":1,"source":"dbSNP","start":140620537,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1484294717","feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140620538,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620538},{"alleles":["G","A","T"],"end":140620541,"strand":1,"feature_type":"variation","start":140620541,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs982739161","seq_region_name":"7","clinical_significance":[]},{"start":140620542,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140620542,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1800249584","clinical_significance":[]},{"end":140620543,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140620543,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs186360931","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620545,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140620545,"id":"rs1327485226","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585771379","source":"dbSNP","start":140620546,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140620546,"alleles":["T","C"],"feature_type":"variation","strand":1},{"end":140620549,"alleles":["T","C","G"],"strand":1,"feature_type":"variation","start":140620549,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1800250203","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620552,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140620552,"id":"rs1195635756","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs529482394","alleles":["T","A","C"],"end":140620554,"feature_type":"variation","strand":1,"source":"dbSNP","start":140620554,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs912593949","clinical_significance":[],"end":140620557,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140620557,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800250921","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620560,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140620560},{"seq_region_name":"7","id":"rs1800251095","clinical_significance":[],"end":140620561,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140620561,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620563,"feature_type":"variation","strand":1,"end":140620563,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs965997925"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800251465","source":"dbSNP","start":140620566,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140620566,"alleles":["A","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1032160286","clinical_significance":[],"start":140620580,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140620580,"alleles":["A","-"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs191830245","seq_region_name":"7","end":140620581,"alleles":["G","C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140620581,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140620587,"alleles":["AA","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620586,"clinical_significance":[],"seq_region_name":"7","id":"rs761182551"},{"clinical_significance":[],"id":"rs1800252262","seq_region_name":"7","feature_type":"variation","strand":1,"end":140620590,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620590},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620594,"feature_type":"variation","strand":1,"end":140620594,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs76881848"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620595,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140620595,"seq_region_name":"7","id":"rs1409873364","clinical_significance":[]},{"end":140620597,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140620597,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1800252611","seq_region_name":"7","clinical_significance":[]},{"id":"rs970712410","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140620598,"strand":1,"feature_type":"variation","start":140620598,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800252831","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620601,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140620601},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140620602,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620602,"source":"dbSNP","seq_region_name":"7","id":"rs1800252941","clinical_significance":[]},{"id":"rs1800253060","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620603,"source":"dbSNP","strand":1,"feature_type":"variation","end":140620603,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1800253144","clinical_significance":[],"alleles":["G","T"],"end":140620604,"strand":1,"feature_type":"variation","start":140620604,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140620607,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620607,"clinical_significance":[],"seq_region_name":"7","id":"rs981186314"},{"clinical_significance":[],"seq_region_name":"7","id":"rs73165443","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620608,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140620608},{"clinical_significance":[],"seq_region_name":"7","id":"rs1165236505","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620610,"feature_type":"variation","strand":1,"end":140620610,"alleles":["G","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130719550","source":"dbSNP","start":140620612,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140620612,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620613,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140620613,"id":"rs6959541","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620617,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140620617,"seq_region_name":"7","id":"rs1417286779","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620620,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140620620,"clinical_significance":[],"id":"rs1800253864","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800253964","end":140620624,"alleles":["GTCTG","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140620620,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563182666","end":140620622,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140620622,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620623,"source":"dbSNP","strand":1,"feature_type":"variation","end":140620623,"alleles":["T","G"],"seq_region_name":"7","id":"rs1585771517","clinical_significance":[]},{"seq_region_name":"7","id":"rs984360302","clinical_significance":[],"end":140620624,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140620624,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140620628,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140620628,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1473600244"},{"seq_region_name":"7","id":"rs913644196","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C","T"],"end":140620629,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620629,"source":"dbSNP"},{"id":"rs1250319090","seq_region_name":"7","clinical_significance":[],"end":140620630,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140620630,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140620631,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","T"],"end":140620631,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs908702638","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800254806","source":"dbSNP","start":140620632,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140620632,"feature_type":"variation","strand":1},{"alleles":["T","C"],"end":140620633,"strand":1,"feature_type":"variation","start":140620633,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130719614","clinical_significance":[]},{"seq_region_name":"7","id":"rs940195483","clinical_significance":[],"end":140620637,"alleles":["CCC","CCCCC"],"strand":1,"feature_type":"variation","start":140620635,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140620636,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620636,"source":"dbSNP","id":"rs1353801849","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","A"],"end":140620639,"feature_type":"variation","strand":1,"source":"dbSNP","start":140620639,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs945134463"},{"seq_region_name":"7","id":"rs1211283806","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620640,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140620640},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620644,"feature_type":"variation","strand":1,"end":140620644,"alleles":["T","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1332282764"},{"start":140620647,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140620647,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1241863058","clinical_significance":[]},{"seq_region_name":"7","id":"rs1046078582","clinical_significance":[],"end":140620651,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140620651,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1800255611","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140620652,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620652,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1272127010","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620658,"source":"dbSNP","strand":1,"feature_type":"variation","end":140620658,"alleles":["T","C"]},{"id":"rs906217527","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140620664,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620664,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1036072903","clinical_significance":[],"start":140620666,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","T"],"end":140620666,"strand":1,"feature_type":"variation"},{"alleles":["G","A"],"end":140620667,"feature_type":"variation","strand":1,"source":"dbSNP","start":140620667,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs570152484"},{"source":"dbSNP","start":140620669,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140620669,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs933119423"},{"end":140620670,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140620670,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1002500504","seq_region_name":"7"},{"clinical_significance":[],"id":"rs1800256397","seq_region_name":"7","source":"dbSNP","start":140620672,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140620672,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1277709803","seq_region_name":"7","alleles":["C","T"],"end":140620675,"feature_type":"variation","strand":1,"source":"dbSNP","start":140620675,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1800256592","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620677,"source":"dbSNP","strand":1,"feature_type":"variation","end":140620677,"alleles":["G","A"]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140620680,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620680,"source":"dbSNP","seq_region_name":"7","id":"rs1800256670","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1050086311","source":"dbSNP","start":140620683,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140620683,"alleles":["C","A","T"],"feature_type":"variation","strand":1},{"id":"rs528052644","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140620686,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620686,"source":"dbSNP"},{"start":140620695,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140620695,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1800256998","clinical_significance":[]},{"seq_region_name":"7","id":"rs537407848","clinical_significance":[],"strand":1,"feature_type":"variation","end":140620696,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620696,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs556206973","source":"dbSNP","start":140620697,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140620697,"feature_type":"variation","strand":1},{"end":140620701,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140620701,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1325237824"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1438401645","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620705,"feature_type":"variation","strand":1,"end":140620705,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1585771779","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620706,"source":"dbSNP","strand":1,"feature_type":"variation","end":140620706,"alleles":["A","C"]},{"alleles":["C","T"],"end":140620710,"feature_type":"variation","strand":1,"source":"dbSNP","start":140620710,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1215567913","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620711,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140620711,"seq_region_name":"7","id":"rs112055167","clinical_significance":[]},{"seq_region_name":"7","id":"rs1000772411","clinical_significance":[],"alleles":["C","A"],"end":140620712,"strand":1,"feature_type":"variation","start":140620712,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs778208948","source":"dbSNP","start":140620715,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","G","T"],"end":140620715,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140620716,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620716,"source":"dbSNP","seq_region_name":"7","id":"rs1026138934","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140620718,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620718,"clinical_significance":[],"seq_region_name":"7","id":"rs1192327932"},{"strand":1,"feature_type":"variation","end":140620726,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620726,"source":"dbSNP","seq_region_name":"7","id":"rs1800258402","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140620728,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620728,"source":"dbSNP","id":"rs1468311039","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","G"],"end":140620730,"strand":1,"feature_type":"variation","start":140620730,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs892282384","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800258708","alleles":["C","T"],"end":140620732,"feature_type":"variation","strand":1,"source":"dbSNP","start":140620732,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140620733,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140620733,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1208894295","clinical_significance":[]},{"seq_region_name":"7","id":"rs1800258913","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140620734,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620734,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140620740,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620740,"clinical_significance":[],"seq_region_name":"7","id":"rs2130719808"},{"alleles":["T","C"],"end":140620741,"strand":1,"feature_type":"variation","start":140620741,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1009815079","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs749797901","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140620742,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620742},{"clinical_significance":[],"id":"rs146375564","seq_region_name":"7","source":"dbSNP","start":140620750,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140620750,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1800259584","clinical_significance":[],"alleles":["G","A"],"end":140620756,"strand":1,"feature_type":"variation","start":140620756,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140620756,"alleles":["G","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140620756,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1800259681"},{"clinical_significance":[],"id":"rs1223179483","seq_region_name":"7","source":"dbSNP","start":140620757,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","-"],"end":140620757,"feature_type":"variation","strand":1},{"alleles":["G","A"],"end":140620758,"feature_type":"variation","strand":1,"source":"dbSNP","start":140620758,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1345682434"},{"seq_region_name":"7","id":"rs951454412","clinical_significance":[],"strand":1,"feature_type":"variation","end":140620760,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620760,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140620762,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620762,"source":"dbSNP","seq_region_name":"7","id":"rs1440473738","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620763,"feature_type":"variation","strand":1,"end":140620763,"alleles":["T","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1004279587"},{"seq_region_name":"7","id":"rs1231881487","clinical_significance":[],"strand":1,"feature_type":"variation","end":140620771,"alleles":["-","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620772,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800260482","feature_type":"variation","strand":1,"end":140620772,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620772},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620776,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140620776,"seq_region_name":"7","id":"rs1025022365","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620777,"source":"dbSNP","strand":1,"feature_type":"variation","end":140620777,"alleles":["C","T"],"seq_region_name":"7","id":"rs1800260688","clinical_significance":[]},{"clinical_significance":[],"id":"rs1180732673","seq_region_name":"7","alleles":["T","A"],"end":140620781,"feature_type":"variation","strand":1,"source":"dbSNP","start":140620781,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1800260890","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","G"],"end":140620786,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620786,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620789,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140620789,"clinical_significance":[],"seq_region_name":"7","id":"rs1019552328"},{"clinical_significance":[],"id":"rs971209993","seq_region_name":"7","source":"dbSNP","start":140620790,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140620790,"alleles":["G","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1321472308","clinical_significance":[],"alleles":["GAG","-"],"end":140620792,"strand":1,"feature_type":"variation","start":140620790,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs186201108","end":140620794,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140620794,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800261406","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140620797,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620797},{"clinical_significance":[],"id":"rs1800261507","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140620798,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620798},{"source":"dbSNP","start":140620807,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140620807,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs965422026"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585772037","source":"dbSNP","start":140620814,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140620814,"alleles":["T","C"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620816,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140620816,"clinical_significance":[],"seq_region_name":"7","id":"rs2130719924"},{"seq_region_name":"7","id":"rs1800261818","clinical_significance":[],"start":140620818,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140620818,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"id":"rs1406125510","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140620832,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620832,"source":"dbSNP"},{"seq_region_name":"7","id":"rs576909592","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["TACAGATGTTTCAATGGGTCCAAAGAGCGATTA","TACAGATGTTTCAATGGGTCCAAAGAGCGATTACAGATGTTTCAATGGGTCCAAAGAGCGATTA"],"end":140620868,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620836,"source":"dbSNP"},{"source":"dbSNP","start":140620842,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140620842,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs976038423"},{"seq_region_name":"7","id":"rs1800262194","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620850,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140620850},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130719948","end":140620851,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140620851,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs921521249","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140620856,"strand":1,"feature_type":"variation","start":140620856,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs771224271","end":140620863,"alleles":["C","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140620863,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["G","A","T"],"end":140620864,"strand":1,"feature_type":"variation","start":140620864,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs796398877","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620870,"feature_type":"variation","strand":1,"end":140620870,"alleles":["G","A"],"clinical_significance":[],"id":"rs1454112697","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800263037","feature_type":"variation","strand":1,"end":140620874,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620874},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140620880,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620880,"clinical_significance":[],"seq_region_name":"7","id":"rs1800263204"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620881,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140620881,"id":"rs1585772083","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1391111381","clinical_significance":[],"alleles":["GG","G"],"end":140620883,"strand":1,"feature_type":"variation","start":140620882,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140620890,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140620890,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1188830070"},{"alleles":["A","C","G"],"end":140620898,"feature_type":"variation","strand":1,"source":"dbSNP","start":140620898,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1800263857"},{"end":140620900,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140620900,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1800264050"},{"seq_region_name":"7","id":"rs1800264185","clinical_significance":[],"strand":1,"feature_type":"variation","end":140620906,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620906,"source":"dbSNP"},{"id":"rs1351418345","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620909,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140620909},{"id":"rs1465944275","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140620910,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620910,"source":"dbSNP"},{"start":140620911,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140620911,"strand":1,"feature_type":"variation","id":"rs914094110","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","G"],"end":140620916,"strand":1,"feature_type":"variation","start":140620916,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1214515966","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140620917,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620917,"clinical_significance":[],"seq_region_name":"7","id":"rs1033622195"},{"source":"dbSNP","start":140620918,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140620918,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs191005958","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs183367347","feature_type":"variation","strand":1,"end":140620927,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620927},{"clinical_significance":[],"id":"rs1800265422","seq_region_name":"7","source":"dbSNP","start":140620928,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140620928,"alleles":["T","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1800265554","clinical_significance":[],"alleles":["C","T"],"end":140620931,"strand":1,"feature_type":"variation","start":140620931,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140620934,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140620934,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1046193311","clinical_significance":[]},{"source":"dbSNP","start":140620935,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140620935,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs558245825"},{"seq_region_name":"7","id":"rs1280732873","clinical_significance":[],"strand":1,"feature_type":"variation","end":140620936,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620936,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140620940,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620940,"source":"dbSNP","seq_region_name":"7","id":"rs1800266172","clinical_significance":[]},{"seq_region_name":"7","id":"rs1800266337","clinical_significance":[],"alleles":["CA","-"],"end":140620944,"strand":1,"feature_type":"variation","start":140620943,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140620945,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140620945,"alleles":["G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs927584328","clinical_significance":[]},{"source":"dbSNP","start":140620946,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140620946,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs937695887","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1376972699","end":140620947,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140620947,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140620949,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140620949,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs984308079"},{"seq_region_name":"7","id":"rs568204425","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620953,"source":"dbSNP","strand":1,"feature_type":"variation","end":140620953,"alleles":["C","T"]},{"clinical_significance":[],"id":"rs1800267276","seq_region_name":"7","source":"dbSNP","start":140620954,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140620954,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs908802412","seq_region_name":"7","alleles":["T","G"],"end":140620956,"feature_type":"variation","strand":1,"source":"dbSNP","start":140620956,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["C","T"],"end":140620957,"feature_type":"variation","strand":1,"source":"dbSNP","start":140620957,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1563182872"},{"seq_region_name":"7","id":"rs1585772239","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620959,"source":"dbSNP","strand":1,"feature_type":"variation","end":140620959,"alleles":["T","C"]},{"seq_region_name":"7","id":"rs1372104015","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140620961,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620961,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620972,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140620972,"clinical_significance":[],"id":"rs1297995614","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1800268246","clinical_significance":[],"strand":1,"feature_type":"variation","end":140620975,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620975,"source":"dbSNP"},{"end":140620984,"alleles":["G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140620984,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1800268399","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140620985,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620985,"source":"dbSNP","seq_region_name":"7","id":"rs115217203","clinical_significance":[]},{"seq_region_name":"7","id":"rs1290970266","clinical_significance":[],"end":140620987,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140620987,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140620993,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140620993,"clinical_significance":[],"seq_region_name":"7","id":"rs1800268891"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140620996,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140620996,"id":"rs1360201477","seq_region_name":"7","clinical_significance":[]},{"end":140621001,"alleles":["ATATA","ATA"],"strand":1,"feature_type":"variation","start":140620997,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs562861355","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800269173","alleles":["T","C"],"end":140620998,"feature_type":"variation","strand":1,"source":"dbSNP","start":140620998,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs543768411","end":140620999,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140620999,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1360901889","clinical_significance":[],"start":140621001,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140621001,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140621003,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621003,"clinical_significance":[],"seq_region_name":"7","id":"rs1311609347"},{"seq_region_name":"7","id":"rs1563182901","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621005,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140621005},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621006,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140621006,"seq_region_name":"7","id":"rs899074549","clinical_significance":[]},{"source":"dbSNP","start":140621007,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140621007,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1337414739"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621009,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140621009,"seq_region_name":"7","id":"rs2130720182","clinical_significance":[]},{"seq_region_name":"7","id":"rs930590855","clinical_significance":[],"strand":1,"feature_type":"variation","end":140621012,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621012,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs78674299","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140621014,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621014},{"seq_region_name":"7","id":"rs772236443","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621015,"source":"dbSNP","strand":1,"feature_type":"variation","end":140621015,"alleles":["C","A"]},{"seq_region_name":"7","id":"rs1800270650","clinical_significance":[],"start":140621019,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140621019,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"id":"rs1273174874","seq_region_name":"7","clinical_significance":[],"start":140621021,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140621021,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1004227009","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621030,"feature_type":"variation","strand":1,"end":140621030,"alleles":["T","C"]},{"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140621033,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621033,"clinical_significance":[],"seq_region_name":"7","id":"rs139755479"},{"seq_region_name":"7","id":"rs1800271270","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621033,"source":"dbSNP","strand":1,"feature_type":"variation","end":140621037,"alleles":["AAAAA","AAAAAA"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621038,"source":"dbSNP","strand":1,"feature_type":"variation","end":140621038,"alleles":["C","G"],"seq_region_name":"7","id":"rs1258930795","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621039,"feature_type":"variation","strand":1,"end":140621044,"alleles":["TTTTTT","TTTTT"],"clinical_significance":[],"seq_region_name":"7","id":"rs1208664416"},{"seq_region_name":"7","id":"rs371028318","clinical_significance":[],"end":140621041,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140621041,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1485279206","clinical_significance":[],"start":140621058,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140621058,"alleles":["C","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1275222137","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140621060,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621060},{"seq_region_name":"7","id":"rs775807351","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621061,"source":"dbSNP","strand":1,"feature_type":"variation","end":140621061,"alleles":["G","A","C"]},{"strand":1,"feature_type":"variation","end":140621064,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621064,"source":"dbSNP","seq_region_name":"7","id":"rs1800272372","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621066,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140621066,"seq_region_name":"7","id":"rs1800272512","clinical_significance":[]},{"id":"rs996848427","seq_region_name":"7","clinical_significance":[],"start":140621068,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140621068,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1028768125","clinical_significance":[],"alleles":["G","A","T"],"end":140621069,"strand":1,"feature_type":"variation","start":140621069,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621073,"feature_type":"variation","strand":1,"end":140621073,"alleles":["G","A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs115287544"},{"alleles":["GG","G"],"end":140621074,"feature_type":"variation","strand":1,"source":"dbSNP","start":140621073,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs2130720273","seq_region_name":"7"},{"seq_region_name":"7","id":"rs989748301","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140621074,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621074,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621078,"feature_type":"variation","strand":1,"end":140621078,"alleles":["G","A"],"clinical_significance":[],"id":"rs1800273386","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140621080,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621080,"source":"dbSNP","seq_region_name":"7","id":"rs1291472157","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621085,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140621085,"seq_region_name":"7","id":"rs888757890","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621099,"feature_type":"variation","strand":1,"end":140621099,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1800273800"},{"seq_region_name":"7","id":"rs1800273895","clinical_significance":[],"alleles":["C","T"],"end":140621100,"strand":1,"feature_type":"variation","start":140621100,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800274010","source":"dbSNP","start":140621101,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140621101,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140621104,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140621104,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1800274113"},{"alleles":["T","C"],"end":140621105,"strand":1,"feature_type":"variation","start":140621105,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1351701001","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130720333","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621108,"source":"dbSNP","strand":1,"feature_type":"variation","end":140621108,"alleles":["A","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1021104921","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621110,"feature_type":"variation","strand":1,"end":140621110,"alleles":["C","T"]},{"source":"dbSNP","start":140621111,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140621111,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs936341889"},{"clinical_significance":[],"seq_region_name":"7","id":"rs966874441","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621113,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140621113},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140621118,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621118,"clinical_significance":[],"id":"rs1800274646","seq_region_name":"7"},{"source":"dbSNP","start":140621123,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140621123,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs981817966"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800274900","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140621124,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621124},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621129,"feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140621129,"clinical_significance":[],"seq_region_name":"7","id":"rs760632627"},{"id":"rs2130720367","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621131,"source":"dbSNP","strand":1,"feature_type":"variation","end":140621131,"alleles":["T","A"]},{"id":"rs1164096242","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621133,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140621133},{"clinical_significance":[],"seq_region_name":"7","id":"rs927733941","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621136,"feature_type":"variation","strand":1,"end":140621136,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800275326","alleles":["T","C"],"end":140621137,"feature_type":"variation","strand":1,"source":"dbSNP","start":140621137,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140621145,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621145,"clinical_significance":[],"seq_region_name":"7","id":"rs1419427831"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621147,"source":"dbSNP","strand":1,"feature_type":"variation","end":140621147,"alleles":["G","A"],"seq_region_name":"7","id":"rs1185205498","clinical_significance":[]},{"id":"rs1800275620","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621149,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","G","T"],"end":140621149},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621153,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140621153,"clinical_significance":[],"seq_region_name":"7","id":"rs1800275758"},{"clinical_significance":[],"seq_region_name":"7","id":"rs559941184","feature_type":"variation","strand":1,"end":140621154,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621154},{"clinical_significance":[],"seq_region_name":"7","id":"rs1252540609","end":140621155,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140621155,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140621159,"alleles":["G","C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621159,"source":"dbSNP","id":"rs1800276052","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621162,"feature_type":"variation","strand":1,"end":140621162,"alleles":["G","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs187747682"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621163,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140621163,"id":"rs1479545748","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140621169,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621169,"clinical_significance":[],"seq_region_name":"7","id":"rs551864168"},{"seq_region_name":"7","id":"rs930540237","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621171,"source":"dbSNP","strand":1,"feature_type":"variation","end":140621171,"alleles":["C","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621172,"source":"dbSNP","strand":1,"feature_type":"variation","end":140621172,"alleles":["G","A"],"seq_region_name":"7","id":"rs1323773509","clinical_significance":[]},{"alleles":["G","A"],"end":140621176,"strand":1,"feature_type":"variation","start":140621176,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs563791038","clinical_significance":[]},{"seq_region_name":"7","id":"rs906389728","clinical_significance":[],"strand":1,"feature_type":"variation","end":140621182,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621182,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1002685187","clinical_significance":[],"end":140621183,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140621183,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800277077","alleles":["A","C","G"],"end":140621184,"feature_type":"variation","strand":1,"source":"dbSNP","start":140621184,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1800277199","clinical_significance":[],"alleles":["G","T"],"end":140621186,"strand":1,"feature_type":"variation","start":140621186,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800277288","alleles":["A","G"],"end":140621194,"feature_type":"variation","strand":1,"source":"dbSNP","start":140621194,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs28687728","source":"dbSNP","start":140621197,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140621197,"alleles":["T","A","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585772688","source":"dbSNP","start":140621198,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140621198,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs952690701","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621198,"feature_type":"variation","strand":1,"alleles":["AAAAAA","AAAA","AAAAA","AAAAAAA"],"end":140621203},{"strand":1,"feature_type":"variation","end":140621201,"alleles":["-","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621202,"source":"dbSNP","seq_region_name":"7","id":"rs1800277801","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621202,"source":"dbSNP","strand":1,"feature_type":"variation","end":140621202,"alleles":["A","C","T"],"seq_region_name":"7","id":"rs531223561","clinical_significance":[]},{"seq_region_name":"7","id":"rs200448547","clinical_significance":[],"end":140621202,"alleles":["-","T","TT"],"strand":1,"feature_type":"variation","start":140621203,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1681778","clinical_significance":[],"alleles":["A","G","T"],"end":140621203,"strand":1,"feature_type":"variation","start":140621203,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140621204,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140621204,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs10225641","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["TTTTTTTTTTTT","TTT","TTTTTTTTTTT","TTTTTTTTTTTTT"],"end":140621215,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621204,"clinical_significance":[],"seq_region_name":"7","id":"rs1015582006"},{"id":"rs1800278489","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["-","G"],"end":140621204,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621205,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140621205,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621205,"clinical_significance":[],"id":"rs183253682","seq_region_name":"7"},{"start":140621206,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140621206,"alleles":["T","A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs547367845","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563183045","feature_type":"variation","strand":1,"end":140621207,"alleles":["T","TGT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621207},{"id":"rs1800278953","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140621208,"alleles":["T","C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621208,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1800279058","seq_region_name":"7","end":140621212,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140621212,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"end":140621216,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140621216,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1357749055","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140621217,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621217,"source":"dbSNP","seq_region_name":"7","id":"rs997361150","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621219,"feature_type":"variation","strand":1,"end":140621219,"alleles":["G","C"],"clinical_significance":[],"id":"rs1800279553","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1231896446","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621225,"feature_type":"variation","strand":1,"end":140621225,"alleles":["G","A","T"]},{"seq_region_name":"7","id":"rs1800279942","clinical_significance":[],"strand":1,"feature_type":"variation","end":140621233,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621233,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1800280112","clinical_significance":[],"alleles":["A","G"],"end":140621235,"strand":1,"feature_type":"variation","start":140621235,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["T","C"],"end":140621236,"feature_type":"variation","strand":1,"source":"dbSNP","start":140621236,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1800280308"},{"feature_type":"variation","strand":1,"end":140621245,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621245,"clinical_significance":[],"seq_region_name":"7","id":"rs1251440087"},{"seq_region_name":"7","id":"rs1213225659","clinical_significance":[],"end":140621246,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140621246,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1293180551","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140621247,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621247,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140621249,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621249,"clinical_significance":[],"id":"rs1028299288","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1800281012","clinical_significance":[],"start":140621259,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140621259,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140621261,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621261,"source":"dbSNP","seq_region_name":"7","id":"rs1800281162","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140621262,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621262,"clinical_significance":[],"seq_region_name":"7","id":"rs1800281297"},{"clinical_significance":[],"seq_region_name":"7","id":"rs985856630","alleles":["A","G"],"end":140621269,"feature_type":"variation","strand":1,"source":"dbSNP","start":140621269,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1262517454","seq_region_name":"7","clinical_significance":[],"end":140621270,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140621270,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140621276,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621276,"clinical_significance":[],"seq_region_name":"7","id":"rs1237560717"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621281,"source":"dbSNP","strand":1,"feature_type":"variation","end":140621281,"alleles":["C","T"],"seq_region_name":"7","id":"rs1316883223","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130720656","clinical_significance":[],"end":140621283,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140621283,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140621284,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621284,"source":"dbSNP","seq_region_name":"7","id":"rs1319165592","clinical_significance":[]},{"alleles":["T","C"],"end":140621285,"strand":1,"feature_type":"variation","start":140621285,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs893824926","clinical_significance":[]},{"end":140621289,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140621289,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1198091070"},{"alleles":["C","G"],"end":140621292,"strand":1,"feature_type":"variation","start":140621292,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1221347654","clinical_significance":[]},{"end":140621299,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140621299,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs910308522"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800282305","source":"dbSNP","start":140621300,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140621300,"alleles":["G","C"],"feature_type":"variation","strand":1},{"alleles":["C","T"],"end":140621301,"strand":1,"feature_type":"variation","start":140621301,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585772944","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621308,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140621308,"id":"rs1270887860","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621309,"source":"dbSNP","strand":1,"feature_type":"variation","end":140621311,"alleles":["ACA","ACAACA"],"seq_region_name":"7","id":"rs1800282599","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140621312,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621312,"clinical_significance":[],"seq_region_name":"7","id":"rs1011128688"},{"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140621320,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621320,"clinical_significance":[],"seq_region_name":"7","id":"rs1800282829"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621324,"feature_type":"variation","strand":1,"end":140621324,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1800282924"},{"start":140621325,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140621325,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs188131051","clinical_significance":[]},{"seq_region_name":"7","id":"rs1290160469","clinical_significance":[],"start":140621326,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140621326,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"end":140621328,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140621328,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs913606082","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1211070452","clinical_significance":[],"start":140621331,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140621331,"strand":1,"feature_type":"variation"},{"start":140621332,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140621332,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1176696659","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140621333,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621333,"source":"dbSNP","id":"rs1800283557","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140621334,"alleles":["G","C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621334,"source":"dbSNP","seq_region_name":"7","id":"rs1259930742","clinical_significance":[]},{"seq_region_name":"7","id":"rs945265786","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140621335,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621335,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1392971758","feature_type":"variation","strand":1,"end":140621336,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621336},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621338,"feature_type":"variation","strand":1,"end":140621338,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1800284027"},{"seq_region_name":"7","id":"rs1186906337","clinical_significance":[],"strand":1,"feature_type":"variation","end":140621341,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621341,"source":"dbSNP"},{"id":"rs1800284251","seq_region_name":"7","clinical_significance":[],"end":140621344,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140621344,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621346,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140621346,"seq_region_name":"7","id":"rs539600034","clinical_significance":[]},{"alleles":["C","T"],"end":140621348,"strand":1,"feature_type":"variation","start":140621348,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs558309189","clinical_significance":[]},{"end":140621349,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140621349,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1203516970"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621351,"feature_type":"variation","strand":1,"end":140621351,"alleles":["T","A"],"clinical_significance":[],"id":"rs1800284932","seq_region_name":"7"},{"source":"dbSNP","start":140621354,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140621354,"alleles":["A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs766270793"},{"seq_region_name":"7","id":"rs142989892","clinical_significance":[],"start":140621358,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140621358,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800285451","source":"dbSNP","start":140621363,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140621363,"alleles":["A","G"],"feature_type":"variation","strand":1},{"start":140621363,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AGA","A"],"end":140621365,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1800285601","clinical_significance":[]},{"seq_region_name":"7","id":"rs1800285748","clinical_significance":[],"strand":1,"feature_type":"variation","end":140621365,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621365,"source":"dbSNP"},{"id":"rs1166094252","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140621367,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621367,"source":"dbSNP"},{"end":140621368,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140621368,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1585773115","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621369,"feature_type":"variation","strand":1,"end":140621369,"alleles":["C","T"],"clinical_significance":[],"id":"rs1346197381","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs990996555","feature_type":"variation","strand":1,"end":140621373,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621373},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621374,"feature_type":"variation","strand":1,"end":140621374,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1055099162"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800286645","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140621381,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621381},{"source":"dbSNP","start":140621382,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140621382,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1800286789"},{"clinical_significance":[],"seq_region_name":"7","id":"rs920247282","source":"dbSNP","start":140621383,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140621383,"alleles":["T","C"],"feature_type":"variation","strand":1},{"end":140621396,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140621396,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1800287115","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1681777","source":"dbSNP","start":140621399,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","G","T"],"end":140621399,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140621399,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140621399,"alleles":["C","-"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs201456320"},{"clinical_significance":[],"seq_region_name":"7","id":"rs754637461","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621400,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140621400},{"end":140621401,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140621401,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs961431463","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1436451890","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140621403,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621403},{"end":140621404,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140621404,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1373428761"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140621405,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621405,"clinical_significance":[],"id":"rs1800288126","seq_region_name":"7"},{"end":140621410,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140621410,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1312603104","clinical_significance":[]},{"id":"rs570033046","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621411,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140621411},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140621414,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621414,"source":"dbSNP","id":"rs114549242","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs116508459","clinical_significance":[],"start":140621415,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C","G"],"end":140621415,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140621418,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","C"],"end":140621418,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs559577947","seq_region_name":"7"},{"feature_type":"variation","strand":1,"end":140621426,"alleles":["TTGTTT","TT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621421,"clinical_significance":[],"seq_region_name":"7","id":"rs1800288676"},{"clinical_significance":[],"id":"rs1428013185","seq_region_name":"7","source":"dbSNP","start":140621424,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140621424,"feature_type":"variation","strand":1},{"id":"rs1256898734","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140621435,"alleles":["AAATAA","AAATAAAATAA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621430,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800288982","alleles":["A","C"],"end":140621432,"feature_type":"variation","strand":1,"source":"dbSNP","start":140621432,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs373840504","source":"dbSNP","start":140621433,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140621433,"alleles":["T","C","G"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140621439,"alleles":["C","CGCTCTCGGCTTTCGGCTCGGAGGAGGCC"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621439,"source":"dbSNP","seq_region_name":"7","id":"rs1219923437","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["-","GCTCTCGGCTTTCGGCTCGG","GCTCTCGGCTTTCGGCTCGGAGGAGGCCAAGGTGCAACTTCCTTCGGTCGTCCCGAATCCGGGTTCATCCGACACCAGCCGCCTCCACCATGCCGCCG"],"end":140621439,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621440,"clinical_significance":[],"seq_region_name":"7","id":"rs1800289156"},{"feature_type":"variation","strand":1,"end":140621440,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621440,"clinical_significance":[],"id":"rs139689267","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621440,"feature_type":"variation","strand":1,"end":140621441,"alleles":["AA","-"],"clinical_significance":[],"id":"rs551886735","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140621441,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621441,"source":"dbSNP","id":"rs1800289464","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1800289565","clinical_significance":[],"start":140621441,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AGAGAAAAATAGTC","-"],"end":140621454,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["G","GGTGCAACTTCCTTCGGTCGTCCCGAATCCGGGTTCATCCGACACCAGCCGCCTCCACCATGCCGCCGAAGTTCGACCCCAACG"],"end":140621442,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621442,"source":"dbSNP","id":"rs1800289655","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","G"],"end":140621449,"feature_type":"variation","strand":1,"source":"dbSNP","start":140621449,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1407432918"},{"id":"rs2130720983","seq_region_name":"7","clinical_significance":[],"end":140621456,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140621456,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs763748144","source":"dbSNP","start":140621457,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140621457,"alleles":["T","C"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140621460,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621460,"source":"dbSNP","seq_region_name":"7","id":"rs985632279","clinical_significance":[]},{"end":140621466,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140621466,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs751197879"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1252705501","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621470,"feature_type":"variation","strand":1,"end":140621470,"alleles":["C","G"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621471,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140621471,"clinical_significance":[],"seq_region_name":"7","id":"rs1224717645"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800290400","source":"dbSNP","start":140621473,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140621473,"alleles":["A","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1800290493","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140621475,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621475,"source":"dbSNP"},{"end":140621479,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140621479,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1800290582","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140621481,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621481,"clinical_significance":[],"id":"rs1210450485","seq_region_name":"7"},{"source":"dbSNP","start":140621482,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140621482,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1471253388"},{"seq_region_name":"7","id":"rs2130721040","clinical_significance":[],"alleles":["T","C"],"end":140621485,"strand":1,"feature_type":"variation","start":140621485,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140621487,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140621487,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1050278081","clinical_significance":[]},{"id":"rs893772580","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621488,"source":"dbSNP","strand":1,"feature_type":"variation","end":140621488,"alleles":["G","T"]},{"alleles":["A","G"],"end":140621492,"strand":1,"feature_type":"variation","start":140621492,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1800291065","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621493,"feature_type":"variation","strand":1,"end":140621493,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1800291166"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1353534429","feature_type":"variation","strand":1,"end":140621494,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621494},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800291340","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621495,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140621495},{"seq_region_name":"7","id":"rs1448589594","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621497,"source":"dbSNP","strand":1,"feature_type":"variation","end":140621497,"alleles":["C","A"]},{"seq_region_name":"7","id":"rs957769722","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621498,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140621498},{"clinical_significance":[],"id":"rs1800291658","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140621499,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621499},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621502,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140621502,"id":"rs989251226","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1800291869","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621504,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140621504},{"clinical_significance":[],"id":"rs533080873","seq_region_name":"7","source":"dbSNP","start":140621510,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140621510,"alleles":["T","C"],"feature_type":"variation","strand":1},{"start":140621511,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140621511,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs755508826","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621514,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140621514,"id":"rs1800292191","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621515,"feature_type":"variation","strand":1,"end":140621515,"alleles":["T","C"],"clinical_significance":[],"id":"rs1800292277","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1800292375","clinical_significance":[],"alleles":["A","T"],"end":140621518,"strand":1,"feature_type":"variation","start":140621518,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1461637207","feature_type":"variation","strand":1,"end":140621522,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621522},{"seq_region_name":"7","id":"rs192087051","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621523,"source":"dbSNP","strand":1,"feature_type":"variation","end":140621523,"alleles":["G","A"]},{"source":"dbSNP","start":140621532,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140621532,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130721133"},{"end":140621534,"alleles":["TGT","T"],"strand":1,"feature_type":"variation","start":140621532,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1800292704","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621533,"feature_type":"variation","strand":1,"alleles":["G","-"],"end":140621533,"clinical_significance":[],"seq_region_name":"7","id":"rs56070144"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621533,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140621533,"seq_region_name":"7","id":"rs78582751","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621533,"source":"dbSNP","strand":1,"feature_type":"variation","end":140621533,"alleles":["G","GG"],"seq_region_name":"7","id":"rs777037723","clinical_significance":[]},{"seq_region_name":"7","id":"rs927905739","clinical_significance":[],"alleles":["T","C","G"],"end":140621534,"strand":1,"feature_type":"variation","start":140621534,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1046719864","seq_region_name":"7","end":140621541,"alleles":["TTTTTTTT","TTTTTTT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140621534,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["T","C"],"end":140621539,"strand":1,"feature_type":"variation","start":140621539,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1439931372","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140621541,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621541,"clinical_significance":[],"id":"rs1248798646","seq_region_name":"7"},{"source":"dbSNP","start":140621544,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140621544,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1800293824"},{"clinical_significance":[],"seq_region_name":"7","id":"rs563525581","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140621546,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621546},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800294039","feature_type":"variation","strand":1,"end":140621557,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621557},{"start":140621559,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140621559,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1338391377","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140621560,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621560,"clinical_significance":[],"id":"rs1273396934","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140621567,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621567,"source":"dbSNP","seq_region_name":"7","id":"rs1800294323","clinical_significance":[]},{"source":"dbSNP","start":140621572,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140621572,"alleles":["T","A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs937963599","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1800294416","clinical_significance":[],"alleles":["T","C"],"end":140621575,"strand":1,"feature_type":"variation","start":140621575,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621576,"feature_type":"variation","strand":1,"end":140621576,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1054882545"},{"strand":1,"feature_type":"variation","end":140621577,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621577,"source":"dbSNP","id":"rs902753619","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800294747","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621578,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140621578},{"alleles":["T","C"],"end":140621580,"feature_type":"variation","strand":1,"source":"dbSNP","start":140621580,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1292600987"},{"seq_region_name":"7","id":"rs1004226908","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140621582,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621582,"source":"dbSNP"},{"end":140621583,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140621583,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs531463679","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140621598,"alleles":["ACAGATACA","ACA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621590,"clinical_significance":[],"seq_region_name":"7","id":"rs1800295098"},{"alleles":["A","T"],"end":140621598,"feature_type":"variation","strand":1,"source":"dbSNP","start":140621598,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1316808157"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621598,"feature_type":"variation","strand":1,"end":140621600,"alleles":["AAA","AA"],"clinical_significance":[],"seq_region_name":"7","id":"rs1563183264"},{"clinical_significance":[],"seq_region_name":"7","id":"rs941437167","alleles":["G","A","T"],"end":140621602,"feature_type":"variation","strand":1,"source":"dbSNP","start":140621602,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140621603,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140621603,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs959821900","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1326311889","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621604,"source":"dbSNP","strand":1,"feature_type":"variation","end":140621604,"alleles":["C","G"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621605,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140621605,"clinical_significance":[],"seq_region_name":"7","id":"rs1800295747"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1437832116","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140621606,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621606},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621608,"feature_type":"variation","strand":1,"alleles":["T","G"],"end":140621608,"clinical_significance":[],"seq_region_name":"7","id":"rs1305643022"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621611,"feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140621611,"clinical_significance":[],"seq_region_name":"7","id":"rs17621746"},{"seq_region_name":"7","id":"rs897126369","clinical_significance":[],"start":140621617,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","T"],"end":140621617,"strand":1,"feature_type":"variation"},{"id":"rs1800296434","seq_region_name":"7","clinical_significance":[],"end":140621618,"alleles":["G","A","C"],"strand":1,"feature_type":"variation","start":140621618,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1027365401","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621622,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140621622},{"seq_region_name":"7","id":"rs1160580550","clinical_significance":[],"alleles":["C","A"],"end":140621628,"strand":1,"feature_type":"variation","start":140621628,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1287088220","source":"dbSNP","start":140621629,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140621629,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1362534972","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621631,"source":"dbSNP","strand":1,"feature_type":"variation","end":140621631,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1585773713","clinical_significance":[],"start":140621634,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140621634,"strand":1,"feature_type":"variation"},{"end":140621635,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140621635,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1800297084","seq_region_name":"7"},{"alleles":["T","C"],"end":140621639,"strand":1,"feature_type":"variation","start":140621639,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1181598426","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140621640,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621640,"clinical_significance":[],"seq_region_name":"7","id":"rs998202435"},{"start":140621643,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140621643,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs796382104","clinical_significance":[]},{"seq_region_name":"7","id":"rs1800297368","clinical_significance":[],"alleles":["G","A"],"end":140621644,"strand":1,"feature_type":"variation","start":140621644,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1215100454","alleles":["C","A"],"end":140621647,"feature_type":"variation","strand":1,"source":"dbSNP","start":140621647,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621651,"source":"dbSNP","strand":1,"feature_type":"variation","end":140621651,"alleles":["C","T"],"id":"rs1203205787","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130721398","source":"dbSNP","start":140621668,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140621668,"feature_type":"variation","strand":1},{"alleles":["G","A"],"end":140621669,"strand":1,"feature_type":"variation","start":140621669,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1466770245","clinical_significance":[]},{"seq_region_name":"7","id":"rs1800297958","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140621670,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621670,"source":"dbSNP"},{"seq_region_name":"7","id":"rs2130721409","clinical_significance":[],"start":140621671,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140621671,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1800298047","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621673,"source":"dbSNP","strand":1,"feature_type":"variation","end":140621673,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs561765332","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621676,"source":"dbSNP","strand":1,"feature_type":"variation","end":140621676,"alleles":["C","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs17621775","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621679,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140621679},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140621680,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621680,"clinical_significance":[],"seq_region_name":"7","id":"rs1007185174"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1352815269","feature_type":"variation","strand":1,"alleles":["A","T"],"end":140621683,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621683},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140621684,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621684,"source":"dbSNP","id":"rs1277689643","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140621685,"alleles":["A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621685,"source":"dbSNP","id":"rs1800298565","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140621686,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140621686,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1452063380","seq_region_name":"7"},{"end":140621690,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140621690,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1800298772","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs184672938","alleles":["G","A","T"],"end":140621695,"feature_type":"variation","strand":1,"source":"dbSNP","start":140621695,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1033158869","clinical_significance":[],"end":140621698,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140621698,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140621704,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C","T"],"end":140621704,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs957553227","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800299245","source":"dbSNP","start":140621713,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140621713,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140621715,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621715,"source":"dbSNP","seq_region_name":"7","id":"rs1800299332","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621719,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140621719,"id":"rs2130721491","seq_region_name":"7","clinical_significance":[]},{"start":140621721,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140621721,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1800299437","clinical_significance":[]},{"alleles":["T","C","G"],"end":140621722,"strand":1,"feature_type":"variation","start":140621722,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs983064473","clinical_significance":[]},{"end":140621723,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140621723,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1250591670"},{"clinical_significance":[],"id":"rs1800299657","seq_region_name":"7","source":"dbSNP","start":140621728,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","A"],"end":140621728,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621730,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140621730,"seq_region_name":"7","id":"rs1800299755","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs907568092","source":"dbSNP","start":140621732,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140621732,"feature_type":"variation","strand":1},{"id":"rs1402499493","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140621733,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621733,"source":"dbSNP"},{"id":"rs1800300325","seq_region_name":"7","clinical_significance":[],"start":140621737,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140621737,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"id":"rs2130721533","seq_region_name":"7","clinical_significance":[],"end":140621739,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140621739,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"alleles":["A","C","T"],"end":140621745,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621745,"clinical_significance":[],"seq_region_name":"7","id":"rs1383503563"},{"clinical_significance":[],"id":"rs1453329586","seq_region_name":"7","source":"dbSNP","start":140621746,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140621746,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140621748,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140621748,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1800300617","seq_region_name":"7"},{"id":"rs1800300765","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140621750,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621750,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1800300930","clinical_significance":[],"end":140621751,"alleles":["AA","A"],"strand":1,"feature_type":"variation","start":140621750,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563183343","source":"dbSNP","start":140621753,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140621753,"alleles":["G","A"],"feature_type":"variation","strand":1},{"alleles":["T","A","G"],"end":140621756,"feature_type":"variation","strand":1,"source":"dbSNP","start":140621756,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs965964029"},{"id":"rs779229616","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621760,"source":"dbSNP","strand":1,"feature_type":"variation","end":140621760,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs1454983933","clinical_significance":[],"start":140621761,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140621761,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs10458275","seq_region_name":"7","source":"dbSNP","start":140621762,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140621762,"alleles":["A","C","G","T"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140621767,"alleles":["AAAA","AAA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621764,"clinical_significance":[],"seq_region_name":"7","id":"rs1800302154"},{"start":140621767,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["ACACA","ACA"],"end":140621771,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585773918","clinical_significance":[]},{"start":140621772,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140621772,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1800302441","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs921751605","feature_type":"variation","strand":1,"end":140621776,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621776},{"strand":1,"feature_type":"variation","end":140621779,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621779,"source":"dbSNP","seq_region_name":"7","id":"rs1800302756","clinical_significance":[]},{"id":"rs1800302936","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140621781,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621781,"source":"dbSNP"},{"seq_region_name":"7","id":"rs927659496","clinical_significance":[],"strand":1,"feature_type":"variation","end":140621793,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621793,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1800303259","clinical_significance":[],"strand":1,"feature_type":"variation","end":140621797,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621797,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621800,"feature_type":"variation","strand":1,"end":140621800,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1251968490"},{"seq_region_name":"7","id":"rs187576670","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621801,"source":"dbSNP","strand":1,"feature_type":"variation","end":140621801,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1448219388","source":"dbSNP","start":140621804,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140621804,"alleles":["C","T"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1282072900","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621805,"feature_type":"variation","strand":1,"end":140621805,"alleles":["A","G"]},{"feature_type":"variation","strand":1,"end":140621807,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621807,"clinical_significance":[],"seq_region_name":"7","id":"rs1800304104"},{"seq_region_name":"7","id":"rs937912719","clinical_significance":[],"alleles":["T","G"],"end":140621810,"strand":1,"feature_type":"variation","start":140621810,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140621811,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140621811,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1800304342","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs990726967","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621812,"feature_type":"variation","strand":1,"end":140621812,"alleles":["G","A","T"]},{"alleles":["A","G"],"end":140621813,"strand":1,"feature_type":"variation","start":140621813,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs151139014","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621814,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140621814,"seq_region_name":"7","id":"rs747270947","clinical_significance":[]},{"seq_region_name":"7","id":"rs1800304826","clinical_significance":[],"end":140621815,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140621815,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800304928","end":140621816,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140621816,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800305034","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621817,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140621817},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140621818,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621818,"clinical_significance":[],"seq_region_name":"7","id":"rs1370593602"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1270971640","feature_type":"variation","strand":1,"end":140621821,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621821},{"source":"dbSNP","start":140621825,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140621825,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs768844186"},{"source":"dbSNP","start":140621827,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140621827,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1328601004"},{"seq_region_name":"7","id":"rs1433058858","clinical_significance":[],"alleles":["G","A"],"end":140621836,"strand":1,"feature_type":"variation","start":140621836,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1585774068","seq_region_name":"7","feature_type":"variation","strand":1,"end":140621839,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621839},{"seq_region_name":"7","id":"rs1054335267","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621840,"source":"dbSNP","strand":1,"feature_type":"variation","end":140621840,"alleles":["A","G"]},{"feature_type":"variation","strand":1,"end":140621841,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621841,"clinical_significance":[],"seq_region_name":"7","id":"rs748255482"},{"clinical_significance":[],"seq_region_name":"7","id":"rs941217892","source":"dbSNP","start":140621842,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140621842,"alleles":["T","A"],"feature_type":"variation","strand":1},{"start":140621843,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["GGGCTGAA","-"],"end":140621850,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130721729","clinical_significance":[]},{"seq_region_name":"7","id":"rs1318260326","clinical_significance":[],"end":140621847,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140621847,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1368862554","seq_region_name":"7","source":"dbSNP","start":140621848,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140621848,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621854,"source":"dbSNP","strand":1,"feature_type":"variation","end":140621854,"alleles":["C","A","G","T"],"seq_region_name":"7","id":"rs1435844443","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140621855,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621855,"clinical_significance":[],"seq_region_name":"7","id":"rs1440330891"},{"start":140621856,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140621856,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs772268154","clinical_significance":[]},{"seq_region_name":"7","id":"rs1037487298","clinical_significance":[],"strand":1,"feature_type":"variation","end":140621857,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621857,"source":"dbSNP"},{"id":"rs915320007","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621858,"source":"dbSNP","strand":1,"feature_type":"variation","end":140621858,"alleles":["T","C"]},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140621859,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621859,"clinical_significance":[],"seq_region_name":"7","id":"rs569843043"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800306919","source":"dbSNP","start":140621861,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140621861,"alleles":["G","T"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140621865,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621865,"source":"dbSNP","seq_region_name":"7","id":"rs776915844","clinical_significance":[]},{"seq_region_name":"7","id":"rs1051098149","clinical_significance":[],"end":140621866,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140621866,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140621870,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140621870,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1337715089","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140621872,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621872,"clinical_significance":[],"seq_region_name":"7","id":"rs1476117736"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621876,"source":"dbSNP","strand":1,"feature_type":"variation","end":140621876,"alleles":["G","A"],"seq_region_name":"7","id":"rs902534772","clinical_significance":[]},{"seq_region_name":"7","id":"rs537596179","clinical_significance":[],"start":140621884,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140621884,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140621887,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140621887,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1800307645"},{"feature_type":"variation","strand":1,"end":140621892,"alleles":["T","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621892,"clinical_significance":[],"seq_region_name":"7","id":"rs1585774227"},{"seq_region_name":"7","id":"rs1800307842","clinical_significance":[],"start":140621898,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140621898,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140621899,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621899,"clinical_significance":[],"seq_region_name":"7","id":"rs1192420566"},{"alleles":["G","C"],"end":140621904,"strand":1,"feature_type":"variation","start":140621904,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1485980319","clinical_significance":[]},{"seq_region_name":"7","id":"rs1800308151","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621905,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140621905},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621907,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140621907,"seq_region_name":"7","id":"rs1282354676","clinical_significance":[]},{"alleles":["A","G"],"end":140621908,"feature_type":"variation","strand":1,"source":"dbSNP","start":140621908,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1800308395"},{"clinical_significance":[],"id":"rs555568497","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","A","G"],"end":140621914,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621914},{"seq_region_name":"7","id":"rs1585774274","clinical_significance":[],"alleles":["G","C"],"end":140621921,"strand":1,"feature_type":"variation","start":140621921,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs887241407","clinical_significance":[],"start":140621923,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C","G"],"end":140621923,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140621927,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621927,"clinical_significance":[],"id":"rs1346873348","seq_region_name":"7"},{"start":140621932,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140621932,"strand":1,"feature_type":"variation","id":"rs1800308971","seq_region_name":"7","clinical_significance":[]},{"end":140621933,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140621933,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1273975289","clinical_significance":[]},{"source":"dbSNP","start":140621938,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140621938,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1800309177"},{"source":"dbSNP","start":140621939,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","T"],"end":140621939,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1007134221","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621942,"source":"dbSNP","strand":1,"feature_type":"variation","end":140621942,"alleles":["G","A","T"],"seq_region_name":"7","id":"rs567659240","clinical_significance":[]},{"seq_region_name":"7","id":"rs1800309534","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621944,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","T"],"end":140621944},{"id":"rs1269718906","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140621949,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621949,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["G","T"],"end":140621950,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621950,"clinical_significance":[],"seq_region_name":"7","id":"rs1800309743"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621951,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140621951,"clinical_significance":[],"id":"rs1415455971","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1057127404","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621961,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140621961},{"alleles":["G","C"],"end":140621964,"feature_type":"variation","strand":1,"source":"dbSNP","start":140621964,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1356795480"},{"seq_region_name":"7","id":"rs1800310146","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621965,"source":"dbSNP","strand":1,"feature_type":"variation","end":140621965,"alleles":["A","G"]},{"clinical_significance":[],"id":"rs895279353","seq_region_name":"7","end":140621966,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140621966,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1800310356","clinical_significance":[],"strand":1,"feature_type":"variation","end":140621967,"alleles":["A","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621967,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140621968,"alleles":["C","A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621968,"clinical_significance":[],"id":"rs1681774","seq_region_name":"7"},{"start":140621969,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140621969,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs73165444","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140621974,"alleles":["A","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621974,"clinical_significance":[],"seq_region_name":"7","id":"rs1800310733"},{"seq_region_name":"7","id":"rs1800310840","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140621976,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621976,"source":"dbSNP"},{"seq_region_name":"7","id":"rs879595297","clinical_significance":[],"alleles":["T","C"],"end":140621981,"strand":1,"feature_type":"variation","start":140621981,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140621984,"feature_type":"variation","strand":1,"end":140621984,"alleles":["A","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs577951841"},{"clinical_significance":[],"id":"rs1800311149","seq_region_name":"7","source":"dbSNP","start":140621986,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","T"],"end":140621986,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1800311255","clinical_significance":[],"end":140621991,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140621991,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1169401027","clinical_significance":[],"strand":1,"feature_type":"variation","end":140621995,"alleles":["G","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140621995,"source":"dbSNP"},{"end":140621996,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140621996,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs545273479","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["G","C","T"],"end":140622000,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622000,"clinical_significance":[],"id":"rs1259607913","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622001,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140622001,"seq_region_name":"7","id":"rs1198675822","clinical_significance":[]},{"id":"rs1585774427","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622003,"source":"dbSNP","strand":1,"feature_type":"variation","end":140622003,"alleles":["C","G"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622004,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140622004,"seq_region_name":"7","id":"rs1800311900","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800312001","source":"dbSNP","start":140622010,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140622010,"feature_type":"variation","strand":1},{"id":"rs1185618981","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140622011,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622011,"source":"dbSNP"},{"source":"dbSNP","start":140622016,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140622016,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1252070900","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800312213","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140622018,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622018},{"seq_region_name":"7","id":"rs1014513377","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140622020,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622020,"source":"dbSNP"},{"source":"dbSNP","start":140622020,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140622021,"alleles":["AA","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130721984"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800312471","source":"dbSNP","start":140622022,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140622022,"alleles":["G","A"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140622023,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622023,"clinical_significance":[],"seq_region_name":"7","id":"rs1233191408"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800312671","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140622026,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622026},{"id":"rs1585774459","seq_region_name":"7","clinical_significance":[],"start":140622028,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140622028,"alleles":["A","T"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140622030,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622030,"source":"dbSNP","seq_region_name":"7","id":"rs1180647403","clinical_significance":[]},{"id":"rs192432564","seq_region_name":"7","clinical_significance":[],"alleles":["T","C"],"end":140622033,"strand":1,"feature_type":"variation","start":140622033,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["A","C"],"end":140622040,"feature_type":"variation","strand":1,"source":"dbSNP","start":140622040,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1800313075"},{"seq_region_name":"7","id":"rs1272552194","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622042,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140622042},{"alleles":["C","T"],"end":140622052,"strand":1,"feature_type":"variation","start":140622052,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1800313175","seq_region_name":"7","clinical_significance":[]},{"id":"rs966107589","seq_region_name":"7","clinical_significance":[],"end":140622053,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140622053,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1475773746","seq_region_name":"7","end":140622055,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140622055,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs975984901","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622059,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140622059},{"seq_region_name":"7","id":"rs1800313543","clinical_significance":[],"start":140622063,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140622063,"alleles":["C","-"],"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140622069,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140622069,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs921842129"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622070,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140622070,"clinical_significance":[],"seq_region_name":"7","id":"rs953355304"},{"id":"rs1034636210","seq_region_name":"7","clinical_significance":[],"end":140622076,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140622076,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1800313957","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622077,"feature_type":"variation","strand":1,"end":140622077,"alleles":["A","G"]},{"id":"rs1800314068","seq_region_name":"7","clinical_significance":[],"start":140622079,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140622079,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1392972919","seq_region_name":"7","source":"dbSNP","start":140622081,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G"],"end":140622081,"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140622086,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622086,"clinical_significance":[],"seq_region_name":"7","id":"rs1291993810"},{"start":140622089,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140622089,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs185568440","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140622092,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622092,"clinical_significance":[],"seq_region_name":"7","id":"rs1800314489"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622093,"source":"dbSNP","strand":1,"feature_type":"variation","end":140622093,"alleles":["G","A"],"seq_region_name":"7","id":"rs959045721","clinical_significance":[]},{"end":140622095,"alleles":["C","A"],"strand":1,"feature_type":"variation","start":140622095,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs989970532","clinical_significance":[]},{"alleles":["T","C"],"end":140622099,"strand":1,"feature_type":"variation","start":140622099,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1800314811","clinical_significance":[]},{"seq_region_name":"7","id":"rs914431986","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140622101,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622101,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140622107,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622107,"clinical_significance":[],"seq_region_name":"7","id":"rs909807503"},{"alleles":["A","C"],"end":140622109,"feature_type":"variation","strand":1,"source":"dbSNP","start":140622109,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1563183546"},{"seq_region_name":"7","id":"rs1800315212","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622110,"source":"dbSNP","strand":1,"feature_type":"variation","end":140622110,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs2130722126","clinical_significance":[],"strand":1,"feature_type":"variation","end":140622116,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622116,"source":"dbSNP"},{"seq_region_name":"7","id":"rs946760946","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622117,"source":"dbSNP","strand":1,"feature_type":"variation","end":140622117,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs978185666","clinical_significance":[],"start":140622118,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140622118,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140622119,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622119,"clinical_significance":[],"seq_region_name":"7","id":"rs375542017"},{"alleles":["G","A","C"],"end":140622120,"strand":1,"feature_type":"variation","start":140622120,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs972587309","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140622122,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622122,"clinical_significance":[],"seq_region_name":"7","id":"rs918453014"},{"source":"dbSNP","start":140622123,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140622123,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs934069843","seq_region_name":"7"},{"source":"dbSNP","start":140622124,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140622124,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1051643493"},{"end":140622127,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140622127,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs939352150"},{"id":"rs1178791994","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140622128,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622128,"source":"dbSNP"},{"source":"dbSNP","start":140622129,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140622129,"alleles":["G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1585774658"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800316461","source":"dbSNP","start":140622130,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140622130,"feature_type":"variation","strand":1},{"id":"rs1306629987","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140622133,"strand":1,"feature_type":"variation","start":140622133,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140622134,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140622134,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1479535279","clinical_significance":[]},{"alleles":["T","C"],"end":140622135,"feature_type":"variation","strand":1,"source":"dbSNP","start":140622135,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1237811656"},{"id":"rs10279057","seq_region_name":"7","clinical_significance":[],"end":140622137,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140622137,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622142,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140622142,"seq_region_name":"7","id":"rs1585774711","clinical_significance":[]},{"seq_region_name":"7","id":"rs759208016","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622143,"source":"dbSNP","strand":1,"feature_type":"variation","end":140622143,"alleles":["A","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs561580090","source":"dbSNP","start":140622144,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140622144,"alleles":["T","C"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs2130722237","clinical_significance":[],"start":140622145,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140622145,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1469895840","source":"dbSNP","start":140622149,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140622149,"feature_type":"variation","strand":1},{"id":"rs1800317790","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140622155,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622155,"source":"dbSNP"},{"source":"dbSNP","start":140622160,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140622160,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs895381851"},{"seq_region_name":"7","id":"rs1232716121","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622161,"source":"dbSNP","strand":1,"feature_type":"variation","end":140622161,"alleles":["G","A"]},{"start":140622163,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140622163,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1800318069","clinical_significance":[]},{"end":140622164,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140622164,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs189295993","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622166,"source":"dbSNP","strand":1,"feature_type":"variation","end":140622166,"alleles":["G","C"],"id":"rs1234950229","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622168,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140622168,"id":"rs948351336","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs540990056","clinical_significance":[],"alleles":["G","A"],"end":140622169,"strand":1,"feature_type":"variation","start":140622169,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140622172,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140622172,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1334003595"},{"end":140622173,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140622173,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1372963980","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1800318831","seq_region_name":"7","end":140622185,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140622185,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622189,"feature_type":"variation","strand":1,"end":140622189,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1308092184"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622191,"source":"dbSNP","strand":1,"feature_type":"variation","end":140622191,"alleles":["A","G"],"id":"rs1800319015","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1441117200","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140622192,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622192},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622201,"feature_type":"variation","strand":1,"end":140622201,"alleles":["C","G"],"clinical_significance":[],"id":"rs1800319219","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1049193743","clinical_significance":[],"end":140622204,"alleles":["C","G"],"strand":1,"feature_type":"variation","start":140622204,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140622208,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622208,"source":"dbSNP","seq_region_name":"7","id":"rs1219183437","clinical_significance":[]},{"seq_region_name":"7","id":"rs1252482666","clinical_significance":[],"strand":1,"feature_type":"variation","end":140622209,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622209,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["C","A","G"],"end":140622210,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622210,"source":"dbSNP","seq_region_name":"7","id":"rs1479409091","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622214,"source":"dbSNP","strand":1,"feature_type":"variation","end":140622214,"alleles":["A","G"],"seq_region_name":"7","id":"rs887958567","clinical_significance":[]},{"end":140622215,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140622215,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1800319898","clinical_significance":[]},{"clinical_significance":[],"id":"rs1800319993","seq_region_name":"7","source":"dbSNP","start":140622216,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140622216,"alleles":["G","T"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140622223,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140622223,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1800320102"},{"seq_region_name":"7","id":"rs1256483580","clinical_significance":[],"alleles":["C","A","T"],"end":140622224,"strand":1,"feature_type":"variation","start":140622224,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1417097045","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140622225,"strand":1,"feature_type":"variation","start":140622225,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"source":"dbSNP","start":140622226,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140622226,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1379404191"},{"clinical_significance":[],"id":"rs1194539839","seq_region_name":"7","feature_type":"variation","strand":1,"end":140622229,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622229},{"clinical_significance":[],"id":"rs1800320634","seq_region_name":"7","source":"dbSNP","start":140622230,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140622230,"alleles":["T","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1585774892","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622232,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140622232},{"strand":1,"feature_type":"variation","end":140622232,"alleles":["C","-"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622232,"source":"dbSNP","seq_region_name":"7","id":"rs1800320862","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622233,"source":"dbSNP","strand":1,"feature_type":"variation","end":140622233,"alleles":["T","C"],"seq_region_name":"7","id":"rs1800320947","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622241,"source":"dbSNP","strand":1,"feature_type":"variation","end":140622241,"alleles":["C","G"],"id":"rs372600744","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1455779792","source":"dbSNP","start":140622241,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","-"],"end":140622241,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1209376363","clinical_significance":[],"start":140622242,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140622242,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140622246,"alleles":["AAAAA","AAAAAA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622242,"source":"dbSNP","seq_region_name":"7","id":"rs1216766296","clinical_significance":[]},{"id":"rs867470323","seq_region_name":"7","clinical_significance":[],"alleles":["A","C"],"end":140622245,"strand":1,"feature_type":"variation","start":140622245,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140622248,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622248,"clinical_significance":[],"seq_region_name":"7","id":"rs1800321541"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800321635","end":140622252,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140622252,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"strand":1,"feature_type":"variation","end":140622256,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622256,"source":"dbSNP","seq_region_name":"7","id":"rs181034654","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622257,"source":"dbSNP","strand":1,"feature_type":"variation","end":140622257,"alleles":["G","A"],"seq_region_name":"7","id":"rs759775888","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800321848","source":"dbSNP","start":140622257,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140622263,"alleles":["GTGGTGG","GTGG"],"feature_type":"variation","strand":1},{"alleles":["G","A"],"end":140622262,"strand":1,"feature_type":"variation","start":140622262,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs533295569","clinical_significance":[]},{"alleles":["A","G"],"end":140622265,"strand":1,"feature_type":"variation","start":140622265,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1800322065","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140622267,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622267,"clinical_significance":[],"seq_region_name":"7","id":"rs2130722447"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622274,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140622274,"clinical_significance":[],"seq_region_name":"7","id":"rs752230046"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622276,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140622276,"clinical_significance":[],"seq_region_name":"7","id":"rs1800322284"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800322410","source":"dbSNP","start":140622280,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140622280,"alleles":["C","A"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1475134307","clinical_significance":[],"end":140622286,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140622286,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140622288,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622288,"source":"dbSNP","seq_region_name":"7","id":"rs1236908756","clinical_significance":[]},{"start":140622289,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140622289,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1372801344","clinical_significance":[]},{"start":140622290,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140622290,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1800322803","clinical_significance":[]},{"seq_region_name":"7","id":"rs1300804151","clinical_significance":[],"start":140622291,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C","T"],"end":140622291,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1171739282","clinical_significance":[],"alleles":["G","C"],"end":140622293,"strand":1,"feature_type":"variation","start":140622293,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622297,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140622297,"clinical_significance":[],"seq_region_name":"7","id":"rs1800323308"},{"seq_region_name":"7","id":"rs1800323403","clinical_significance":[],"start":140622298,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140622298,"alleles":["A","-"],"strand":1,"feature_type":"variation"},{"end":140622300,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140622300,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1290586112"},{"start":140622303,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140622303,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1003266576","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585775038","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140622304,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622304,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140622306,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622306,"source":"dbSNP","id":"rs1359792710","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","C"],"end":140622309,"strand":1,"feature_type":"variation","start":140622309,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1174078578","seq_region_name":"7","clinical_significance":[]},{"start":140622310,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140622310,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs184869700","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs138999698","source":"dbSNP","start":140622311,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A","T"],"end":140622311,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1297790740","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140622312,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622312},{"strand":1,"feature_type":"variation","end":140622318,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622318,"source":"dbSNP","seq_region_name":"7","id":"rs1800324456","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622322,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","T"],"end":140622322,"seq_region_name":"7","id":"rs1198343713","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1028686845","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622327,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140622327},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622328,"feature_type":"variation","strand":1,"end":140622328,"alleles":["G","A"],"clinical_significance":[],"id":"rs530579978","seq_region_name":"7"},{"start":140622332,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","T"],"end":140622332,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1016591923","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622339,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140622339,"seq_region_name":"7","id":"rs1585775122","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140622342,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622342,"clinical_significance":[],"seq_region_name":"7","id":"rs549460458"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140622343,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622343,"clinical_significance":[],"seq_region_name":"7","id":"rs1310784388"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1021440624","alleles":["G","A","C"],"end":140622344,"feature_type":"variation","strand":1,"source":"dbSNP","start":140622344,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1800325293","clinical_significance":[],"alleles":["A","G"],"end":140622345,"strand":1,"feature_type":"variation","start":140622345,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1585775162","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622353,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140622353},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622354,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140622354,"clinical_significance":[],"seq_region_name":"7","id":"rs1585775172"},{"source":"dbSNP","start":140622356,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140622356,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1800325591"},{"seq_region_name":"7","id":"rs1252850987","clinical_significance":[],"end":140622358,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140622358,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1346087329","seq_region_name":"7","alleles":["C","T"],"end":140622360,"feature_type":"variation","strand":1,"source":"dbSNP","start":140622360,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs997276870","clinical_significance":[],"end":140622361,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140622361,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1800325972","clinical_significance":[],"strand":1,"feature_type":"variation","end":140622370,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622370,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1800326057","clinical_significance":[],"alleles":["G","C"],"end":140622371,"strand":1,"feature_type":"variation","start":140622371,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["C","G","T"],"end":140622374,"strand":1,"feature_type":"variation","start":140622374,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs918412633","clinical_significance":[]},{"source":"dbSNP","start":140622375,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140622375,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs567626143"},{"alleles":["C","A"],"end":140622377,"feature_type":"variation","strand":1,"source":"dbSNP","start":140622377,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1800326365"},{"alleles":["A","C","G"],"end":140622378,"feature_type":"variation","strand":1,"source":"dbSNP","start":140622378,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs535032883"},{"clinical_significance":[],"id":"rs955396468","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622378,"feature_type":"variation","strand":1,"alleles":["AGAG","AG"],"end":140622381},{"clinical_significance":[],"id":"rs1226115349","seq_region_name":"7","feature_type":"variation","strand":1,"end":140622379,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622379},{"seq_region_name":"7","id":"rs2130722648","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["CTC","CTCTC"],"end":140622389,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622387,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1800326825","clinical_significance":[],"alleles":["C","T"],"end":140622390,"strand":1,"feature_type":"variation","start":140622390,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140622392,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140622392,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1800326908","clinical_significance":[]},{"alleles":["C","A","T"],"end":140622395,"strand":1,"feature_type":"variation","start":140622395,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1397565849","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs879906984","feature_type":"variation","strand":1,"alleles":["AAAAAAAAAAAAA","AAAAAAAAAAAA","AAAAAAAAAAAAAA"],"end":140622408,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622396},{"alleles":["A","G"],"end":140622398,"strand":1,"feature_type":"variation","start":140622398,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1373330037","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800327438","end":140622403,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140622403,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1172231830","end":140622404,"alleles":["-","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140622405,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140622408,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622408,"clinical_significance":[],"seq_region_name":"7","id":"rs1800327643"},{"id":"rs942642884","seq_region_name":"7","clinical_significance":[],"start":140622409,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","A"],"end":140622409,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622412,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140622412,"clinical_significance":[],"seq_region_name":"7","id":"rs62485843"},{"start":140622413,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140622413,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1800327966","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140622417,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622417,"source":"dbSNP","seq_region_name":"7","id":"rs1208297635","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1168483557","source":"dbSNP","start":140622424,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140622424,"alleles":["T","C"],"feature_type":"variation","strand":1},{"end":140622428,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140622428,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1800328325"},{"clinical_significance":[],"id":"rs1800328411","seq_region_name":"7","source":"dbSNP","start":140622429,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140622429,"alleles":["A","G"],"feature_type":"variation","strand":1},{"id":"rs753398509","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140622435,"strand":1,"feature_type":"variation","start":140622435,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140622440,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622440,"source":"dbSNP","seq_region_name":"7","id":"rs1800328618","clinical_significance":[]},{"id":"rs1477535862","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140622441,"strand":1,"feature_type":"variation","start":140622441,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs967214157","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622442,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140622442},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140622443,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622443,"clinical_significance":[],"seq_region_name":"7","id":"rs1800328963"},{"alleles":["C","T"],"end":140622446,"feature_type":"variation","strand":1,"source":"dbSNP","start":140622446,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs552977921"},{"seq_region_name":"7","id":"rs1585775320","clinical_significance":[],"alleles":["A","G"],"end":140622447,"strand":1,"feature_type":"variation","start":140622447,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["A","C"],"end":140622451,"feature_type":"variation","strand":1,"source":"dbSNP","start":140622451,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs978133411"},{"alleles":["T","C"],"end":140622452,"feature_type":"variation","strand":1,"source":"dbSNP","start":140622452,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1800329363"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622455,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140622455,"clinical_significance":[],"seq_region_name":"7","id":"rs1585775332"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622456,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140622456,"clinical_significance":[],"seq_region_name":"7","id":"rs1800329577"},{"clinical_significance":[],"id":"rs914600123","seq_region_name":"7","alleles":["ACA","A"],"end":140622458,"feature_type":"variation","strand":1,"source":"dbSNP","start":140622456,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622457,"source":"dbSNP","strand":1,"feature_type":"variation","end":140622457,"alleles":["C","T"],"id":"rs2130722780","seq_region_name":"7","clinical_significance":[]},{"id":"rs1800329802","seq_region_name":"7","clinical_significance":[],"alleles":["A","G"],"end":140622460,"strand":1,"feature_type":"variation","start":140622460,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1187588811","clinical_significance":[],"end":140622465,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140622465,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs2130722792","clinical_significance":[],"start":140622468,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140622468,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"start":140622469,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140622469,"alleles":["A","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1484910754","clinical_significance":[]},{"end":140622470,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140622470,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs2130722804","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1264528126","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622472,"feature_type":"variation","strand":1,"end":140622472,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1585775359","clinical_significance":[],"strand":1,"feature_type":"variation","end":140622478,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622478,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140622483,"alleles":["ATCCAA","ATCCAATCCAA"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622478,"source":"dbSNP","seq_region_name":"7","id":"rs1196716483","clinical_significance":[]},{"alleles":["T","A"],"end":140622479,"feature_type":"variation","strand":1,"source":"dbSNP","start":140622479,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs76046834","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622480,"source":"dbSNP","strand":1,"feature_type":"variation","end":140622480,"alleles":["C","G"],"seq_region_name":"7","id":"rs939487987","clinical_significance":[]},{"id":"rs1800330969","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140622481,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622481,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140622483,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622483,"clinical_significance":[],"seq_region_name":"7","id":"rs1042376105"},{"alleles":["C","T"],"end":140622487,"strand":1,"feature_type":"variation","start":140622487,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1800331199","clinical_significance":[]},{"start":140622495,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140622495,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1316675013","clinical_significance":[]},{"seq_region_name":"7","id":"rs543240666","clinical_significance":[],"start":140622500,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140622500,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585775418","source":"dbSNP","start":140622501,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140622501,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs538986763","source":"dbSNP","start":140622502,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140622502,"alleles":["G","T"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622503,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140622503,"id":"rs189697793","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622504,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140622504,"clinical_significance":[],"seq_region_name":"7","id":"rs1338514761"},{"alleles":["C","G"],"end":140622505,"feature_type":"variation","strand":1,"source":"dbSNP","start":140622505,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1800332101"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622505,"feature_type":"variation","strand":1,"alleles":["CCTCCTCCTC","CCTCCTC"],"end":140622514,"clinical_significance":[],"seq_region_name":"7","id":"rs1800332202"},{"clinical_significance":[],"seq_region_name":"7","id":"rs916601384","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622507,"feature_type":"variation","strand":1,"end":140622507,"alleles":["T","C"]},{"feature_type":"variation","strand":1,"end":140622514,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622514,"clinical_significance":[],"seq_region_name":"7","id":"rs1800332416"},{"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140622517,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622517,"source":"dbSNP","id":"rs1800332511","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140622520,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140622520,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs948276827","seq_region_name":"7"},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140622521,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622521,"source":"dbSNP","seq_region_name":"7","id":"rs1800332722","clinical_significance":[]},{"seq_region_name":"7","id":"rs1800332819","clinical_significance":[],"start":140622522,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140622522,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"id":"rs1800332928","seq_region_name":"7","clinical_significance":[],"end":140622523,"alleles":["T","A"],"strand":1,"feature_type":"variation","start":140622523,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800333038","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622528,"feature_type":"variation","strand":1,"end":140622528,"alleles":["T","A"]},{"id":"rs1049306493","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140622529,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622529,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140622531,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622531,"clinical_significance":[],"seq_region_name":"7","id":"rs1391734607"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1430483976","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622532,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140622532},{"id":"rs149883912","seq_region_name":"7","clinical_significance":[],"start":140622536,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140622536,"strand":1,"feature_type":"variation"},{"end":140622537,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140622537,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1056108523"},{"clinical_significance":[],"id":"rs1800333666","seq_region_name":"7","feature_type":"variation","strand":1,"end":140622547,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622547},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140622548,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622548,"source":"dbSNP","seq_region_name":"7","id":"rs1800333761","clinical_significance":[]},{"clinical_significance":[],"id":"rs1465183052","seq_region_name":"7","feature_type":"variation","strand":1,"end":140622551,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622551},{"seq_region_name":"7","id":"rs1800333962","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622552,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140622552},{"seq_region_name":"7","id":"rs1800334060","clinical_significance":[],"strand":1,"feature_type":"variation","end":140622559,"alleles":["C","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622559,"source":"dbSNP"},{"end":140622562,"alleles":["T","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140622562,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1800334234"},{"clinical_significance":[],"id":"rs1800334378","seq_region_name":"7","end":140622563,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140622563,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130722949","source":"dbSNP","start":140622564,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140622564,"feature_type":"variation","strand":1},{"source":"dbSNP","start":140622567,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140622567,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1418608093"},{"id":"rs1800334689","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140622568,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622568,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140622569,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622569,"source":"dbSNP","id":"rs1167782384","seq_region_name":"7","clinical_significance":[]},{"alleles":["TCAGGAGCCTTCAG","TCAG"],"end":140622583,"strand":1,"feature_type":"variation","start":140622570,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1172075846","seq_region_name":"7","clinical_significance":[]},{"id":"rs1474538219","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622572,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140622572},{"start":140622577,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140622577,"alleles":["C","G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1800335345","clinical_significance":[]},{"start":140622582,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140622582,"alleles":["A","G"],"strand":1,"feature_type":"variation","id":"rs2130722975","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1374606832","clinical_significance":[],"alleles":["G","A"],"end":140622583,"strand":1,"feature_type":"variation","start":140622583,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622586,"source":"dbSNP","strand":1,"feature_type":"variation","end":140622586,"alleles":["C","A"],"seq_region_name":"7","id":"rs940858110","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1431268371","source":"dbSNP","start":140622590,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140622590,"alleles":["T","C"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622591,"feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140622591,"clinical_significance":[],"seq_region_name":"7","id":"rs1183064527"},{"seq_region_name":"7","id":"rs1421244110","clinical_significance":[],"end":140622594,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140622594,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1252231158","seq_region_name":"7","clinical_significance":[],"end":140622601,"alleles":["G","C"],"strand":1,"feature_type":"variation","start":140622601,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800336368","alleles":["G","T"],"end":140622608,"feature_type":"variation","strand":1,"source":"dbSNP","start":140622608,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["A","C"],"end":140622609,"strand":1,"feature_type":"variation","start":140622609,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1800336467","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1290529730","source":"dbSNP","start":140622614,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140622614,"feature_type":"variation","strand":1},{"id":"rs1036523249","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140622618,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622618,"source":"dbSNP"},{"end":140622622,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140622622,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585775647","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1359734761","feature_type":"variation","strand":1,"end":140622623,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622623},{"seq_region_name":"7","id":"rs1639968","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140622625,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622625,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1354221527","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622628,"feature_type":"variation","strand":1,"end":140622628,"alleles":["A","G"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622633,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140622633,"seq_region_name":"7","id":"rs1283511185","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800337185","source":"dbSNP","start":140622634,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140622634,"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140622638,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622638,"source":"dbSNP","id":"rs1800337283","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","T"],"end":140622640,"strand":1,"feature_type":"variation","start":140622640,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1239512231","clinical_significance":[]},{"alleles":["C","T"],"end":140622645,"strand":1,"feature_type":"variation","start":140622645,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1800337508","clinical_significance":[]},{"source":"dbSNP","start":140622647,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140622647,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1303427487"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622648,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140622648,"clinical_significance":[],"seq_region_name":"7","id":"rs1800337736"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622651,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140622651,"seq_region_name":"7","id":"rs1337251090","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs758633617","feature_type":"variation","strand":1,"end":140622653,"alleles":["A","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622653},{"clinical_significance":[],"seq_region_name":"7","id":"rs1395461474","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622658,"feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140622658},{"seq_region_name":"7","id":"rs1585775723","clinical_significance":[],"alleles":["A","C"],"end":140622665,"strand":1,"feature_type":"variation","start":140622665,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1585775725","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622666,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140622666},{"clinical_significance":[],"id":"rs1800338501","seq_region_name":"7","source":"dbSNP","start":140622667,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140622667,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1328066383","clinical_significance":[],"end":140622670,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140622670,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140622671,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140622671,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1231622756","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622675,"feature_type":"variation","strand":1,"end":140622675,"alleles":["C","T"],"clinical_significance":[],"id":"rs1403667779","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622677,"feature_type":"variation","strand":1,"end":140622677,"alleles":["G","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1800338927"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1011992601","source":"dbSNP","start":140622678,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140622678,"alleles":["C","A","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs780527353","clinical_significance":[],"strand":1,"feature_type":"variation","end":140622685,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622685,"source":"dbSNP"},{"id":"rs555452898","seq_region_name":"7","clinical_significance":[],"end":140622686,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140622686,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"start":140622692,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140622692,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1362370967","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622696,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140622696,"seq_region_name":"7","id":"rs1800339475","clinical_significance":[]},{"source":"dbSNP","start":140622697,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140622697,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1216901272"},{"alleles":["GGGGG","GGGGGG"],"end":140622706,"strand":1,"feature_type":"variation","start":140622702,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs962719604","clinical_significance":[]},{"end":140622703,"alleles":["G","A","C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140622703,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1176428888"},{"source":"dbSNP","start":140622704,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140622704,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1800340031"},{"alleles":["G","A"],"end":140622705,"feature_type":"variation","strand":1,"source":"dbSNP","start":140622705,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1438738362"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1253213979","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622706,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140622706},{"alleles":["A","-"],"end":140622707,"strand":1,"feature_type":"variation","start":140622707,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1800340414","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs994068476","alleles":["G","A"],"end":140622712,"feature_type":"variation","strand":1,"source":"dbSNP","start":140622712,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140622716,"alleles":["A","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622716,"clinical_significance":[],"seq_region_name":"7","id":"rs1195017602"},{"source":"dbSNP","start":140622722,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140622728,"alleles":["TCCTTCT","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1800340727","seq_region_name":"7"},{"end":140622723,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140622723,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1800340822"},{"feature_type":"variation","strand":1,"end":140622744,"alleles":["CTTCTTCTTCTTCTTCTTCTT","CTTCTTCTTCTTCTT","CTTCTTCTTCTTCTTCTT","CTTCTTCTTCTTCTTCTTCTTCTT","CTTCTTCTTCTTCTTCTTCTTCTTCTT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622724,"clinical_significance":[],"id":"rs144845111","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1283676005","clinical_significance":[],"alleles":["T","C"],"end":140622726,"strand":1,"feature_type":"variation","start":140622726,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1262887715","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622736,"feature_type":"variation","strand":1,"end":140622736,"alleles":["C","A","T"]},{"seq_region_name":"7","id":"rs1800341437","clinical_significance":[],"start":140622737,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140622747,"alleles":["TTCTTCTTATT","TT"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800341537","source":"dbSNP","start":140622737,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140622750,"alleles":["TTCTTCTTATTTTT","TT"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800341649","source":"dbSNP","start":140622739,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140622739,"feature_type":"variation","strand":1},{"id":"rs1800341803","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140622743,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622743,"source":"dbSNP"},{"alleles":["TTATT","TT"],"end":140622747,"strand":1,"feature_type":"variation","start":140622743,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1485143475","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622743,"feature_type":"variation","strand":1,"end":140622752,"alleles":["TTATTTTTAT","TTAT"],"clinical_significance":[],"seq_region_name":"7","id":"rs1305897383"},{"clinical_significance":[],"id":"rs1681773","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140622744,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622744},{"id":"rs1021557197","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622745,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140622745},{"feature_type":"variation","strand":1,"end":140622747,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622747,"clinical_significance":[],"seq_region_name":"7","id":"rs1800342383"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622748,"feature_type":"variation","strand":1,"alleles":["T","C","G"],"end":140622748,"clinical_significance":[],"seq_region_name":"7","id":"rs1585775928"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622749,"feature_type":"variation","strand":1,"end":140622749,"alleles":["T","C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1455679805"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622751,"source":"dbSNP","strand":1,"feature_type":"variation","end":140622751,"alleles":["A","T"],"seq_region_name":"7","id":"rs967328888","clinical_significance":[]},{"id":"rs1402907835","seq_region_name":"7","clinical_significance":[],"start":140622753,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140622753,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140622754,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622754,"source":"dbSNP","id":"rs1359152565","seq_region_name":"7","clinical_significance":[]},{"end":140622762,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140622762,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1800343087"},{"start":140622763,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140622763,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1394752546","clinical_significance":[]},{"seq_region_name":"7","id":"rs1800343316","clinical_significance":[],"alleles":["T","G"],"end":140622767,"strand":1,"feature_type":"variation","start":140622767,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1401537748","clinical_significance":[],"strand":1,"feature_type":"variation","end":140622773,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622773,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140622777,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622777,"clinical_significance":[],"id":"rs1371984701","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622780,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140622780,"clinical_significance":[],"seq_region_name":"7","id":"rs1800343757"},{"seq_region_name":"7","id":"rs368734687","clinical_significance":[],"start":140622783,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140622783,"alleles":["G","A","C"],"strand":1,"feature_type":"variation"},{"start":140622784,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140622784,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585776002","clinical_significance":[]},{"clinical_significance":[],"id":"rs1800344062","seq_region_name":"7","alleles":["G","T"],"end":140622787,"feature_type":"variation","strand":1,"source":"dbSNP","start":140622787,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"id":"rs1800344219","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622789,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140622789},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800344368","end":140622798,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140622798,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140622799,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622799,"clinical_significance":[],"seq_region_name":"7","id":"rs541108519"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622800,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140622800,"clinical_significance":[],"seq_region_name":"7","id":"rs574958836"},{"seq_region_name":"7","id":"rs1800344850","clinical_significance":[],"strand":1,"feature_type":"variation","end":140622801,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622801,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800345019","source":"dbSNP","start":140622803,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140622803,"feature_type":"variation","strand":1},{"alleles":["T","C"],"end":140622804,"strand":1,"feature_type":"variation","start":140622804,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1461997368","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["AG","-"],"end":140622807,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622806,"clinical_significance":[],"seq_region_name":"7","id":"rs1800345291"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622811,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140622811,"id":"rs914551682","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1245584530","clinical_significance":[],"start":140622812,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140622812,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1193237023","feature_type":"variation","strand":1,"end":140622819,"alleles":["G","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622819},{"start":140622823,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140622823,"strand":1,"feature_type":"variation","id":"rs1800345941","seq_region_name":"7","clinical_significance":[]},{"alleles":["T","C"],"end":140622829,"feature_type":"variation","strand":1,"source":"dbSNP","start":140622829,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1035560103"},{"alleles":["A","G"],"end":140622832,"strand":1,"feature_type":"variation","start":140622832,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1800346245","clinical_significance":[]},{"clinical_significance":[],"id":"rs1800346400","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140622836,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622836},{"end":140622838,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140622838,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1448718101","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622839,"feature_type":"variation","strand":1,"alleles":["T","A","C"],"end":140622839,"clinical_significance":[],"id":"rs961050473","seq_region_name":"7"},{"alleles":["G","A"],"end":140622842,"feature_type":"variation","strand":1,"source":"dbSNP","start":140622842,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs946058338","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1800347081","clinical_significance":[],"start":140622847,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140622847,"strand":1,"feature_type":"variation"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622850,"source":"dbSNP","strand":1,"feature_type":"variation","end":140622850,"alleles":["G","T"],"seq_region_name":"7","id":"rs769038150","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs776829241","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622851,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140622851},{"id":"rs181481085","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A","C"],"end":140622852,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622852,"source":"dbSNP"},{"start":140622854,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140622854,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs2130723424","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140622854,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["GAG","G"],"end":140622856,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1800347513","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1344432451","clinical_significance":[],"end":140622857,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140622857,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1372524110","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622859,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140622859},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800348066","alleles":["C","G"],"end":140622866,"feature_type":"variation","strand":1,"source":"dbSNP","start":140622866,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"end":140622869,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622869,"clinical_significance":[],"seq_region_name":"7","id":"rs916533485"},{"end":140622874,"alleles":["T","-"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140622874,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1800348430","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800348575","feature_type":"variation","strand":1,"end":140622875,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622875},{"strand":1,"feature_type":"variation","end":140622879,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622879,"source":"dbSNP","seq_region_name":"7","id":"rs1800348748","clinical_significance":[]},{"end":140622880,"alleles":["C","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140622880,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs969361812","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1432948685","feature_type":"variation","strand":1,"end":140622881,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622881},{"start":140622882,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140622882,"strand":1,"feature_type":"variation","id":"rs1800349165","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140622889,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622889,"clinical_significance":[],"seq_region_name":"7","id":"rs1800349270"},{"seq_region_name":"7","id":"rs1800349377","clinical_significance":[],"start":140622891,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140622891,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs372916297","clinical_significance":[],"start":140622892,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140622892,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs2130723509","seq_region_name":"7","alleles":["A","C"],"end":140622893,"feature_type":"variation","strand":1,"source":"dbSNP","start":140622893,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1800349603","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622893,"source":"dbSNP","strand":1,"feature_type":"variation","end":140622894,"alleles":["AA","-"]},{"feature_type":"variation","strand":1,"end":140622894,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622894,"clinical_significance":[],"seq_region_name":"7","id":"rs1302098870"},{"alleles":["G","T"],"end":140622909,"feature_type":"variation","strand":1,"source":"dbSNP","start":140622909,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1415800302"},{"alleles":["C","G"],"end":140622910,"feature_type":"variation","strand":1,"source":"dbSNP","start":140622910,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1800349916","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622911,"source":"dbSNP","strand":1,"feature_type":"variation","end":140622911,"alleles":["T","C"],"seq_region_name":"7","id":"rs1800350013","clinical_significance":[]},{"end":140622912,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140622912,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1800350119"},{"end":140622935,"alleles":["GCTGAGTAAACTTTGGCTGCT","GCTGAGTAAACTTTGGCTGCTGAGTAAACTTTGGCTGCT"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140622915,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1377603418","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1800350328","clinical_significance":[],"start":140622918,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140622918,"strand":1,"feature_type":"variation"},{"end":140622920,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140622920,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1800350432","clinical_significance":[]},{"seq_region_name":"7","id":"rs748189729","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622921,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C","G"],"end":140622921},{"end":140622924,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140622924,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1225128281","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs984795439","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140622925,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622925},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563184002","source":"dbSNP","start":140622926,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140622926,"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622932,"feature_type":"variation","strand":1,"end":140622932,"alleles":["T","A","G"],"clinical_significance":[],"id":"rs1800351044","seq_region_name":"7"},{"seq_region_name":"7","id":"rs928888011","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140622935,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622935,"source":"dbSNP"},{"start":140622936,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140622936,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1800351318","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs762507934","alleles":["A","T"],"end":140622937,"feature_type":"variation","strand":1,"source":"dbSNP","start":140622937,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1800351554","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622941,"source":"dbSNP","strand":1,"feature_type":"variation","end":140622941,"alleles":["A","G"]},{"source":"dbSNP","start":140622943,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140622943,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1478515893"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800351806","alleles":["C","-"],"end":140622943,"feature_type":"variation","strand":1,"source":"dbSNP","start":140622943,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1800351921","seq_region_name":"7","clinical_significance":[],"end":140622945,"alleles":["A","T"],"strand":1,"feature_type":"variation","start":140622945,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1421397371","source":"dbSNP","start":140622951,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140622951,"alleles":["C","G"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1192776404","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","G"],"end":140622955,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622955,"source":"dbSNP"},{"id":"rs770024873","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140622957,"alleles":["A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622957,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1208632565","feature_type":"variation","strand":1,"end":140622966,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622966},{"clinical_significance":[],"seq_region_name":"7","id":"rs1259301309","feature_type":"variation","strand":1,"end":140622967,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622967},{"alleles":["T","C"],"end":140622973,"strand":1,"feature_type":"variation","start":140622973,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1800353094","clinical_significance":[]},{"start":140622978,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140622978,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1207714473","clinical_significance":[]},{"source":"dbSNP","start":140622983,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","C"],"end":140622983,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130723617"},{"id":"rs147576638","seq_region_name":"7","clinical_significance":[],"start":140622985,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140622985,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140622988,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622988,"clinical_significance":[],"seq_region_name":"7","id":"rs1800353550"},{"seq_region_name":"7","id":"rs1273958113","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140622990,"source":"dbSNP","strand":1,"feature_type":"variation","end":140622990,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs940976000","source":"dbSNP","start":140622992,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140622992,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs2130723635","clinical_significance":[],"start":140622996,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140622996,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800353997","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140622998,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140622998},{"strand":1,"feature_type":"variation","end":140623000,"alleles":["T","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623000,"source":"dbSNP","seq_region_name":"7","id":"rs545333443","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623001,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140623001,"clinical_significance":[],"seq_region_name":"7","id":"rs1800354318"},{"seq_region_name":"7","id":"rs185722146","clinical_significance":[],"start":140623006,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140623006,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140623010,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140623010,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs933037004","seq_region_name":"7"},{"start":140623013,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140623013,"alleles":["T","C"],"strand":1,"feature_type":"variation","id":"rs1800354838","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140623015,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140623015,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1278147157"},{"id":"rs1800355114","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140623019,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623019,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1800355262","seq_region_name":"7","end":140623020,"alleles":["GG","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140623019,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623020,"source":"dbSNP","strand":1,"feature_type":"variation","end":140623020,"alleles":["G","A"],"seq_region_name":"7","id":"rs1800355427","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140623024,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623024,"clinical_significance":[],"seq_region_name":"7","id":"rs1050192593"},{"feature_type":"variation","strand":1,"end":140623027,"alleles":["G","A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623027,"clinical_significance":[],"id":"rs888746524","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800355935","feature_type":"variation","strand":1,"end":140623030,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623030},{"source":"dbSNP","start":140623034,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140623034,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1011246295"},{"seq_region_name":"7","id":"rs1800356261","clinical_significance":[],"start":140623041,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140623041,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"start":140623045,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["CCC","CC"],"end":140623047,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1447751802","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1358289146","source":"dbSNP","start":140623046,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140623046,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs190576598","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623049,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140623049},{"start":140623050,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140623050,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1329040032","clinical_significance":[]},{"seq_region_name":"7","id":"rs1466747657","clinical_significance":[],"strand":1,"feature_type":"variation","end":140623051,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623051,"source":"dbSNP"},{"id":"rs1179175182","seq_region_name":"7","clinical_significance":[],"start":140623052,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140623052,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1042779908","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623053,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140623053},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623054,"source":"dbSNP","strand":1,"feature_type":"variation","end":140623054,"alleles":["G","A","C","T"],"seq_region_name":"7","id":"rs903090889","clinical_significance":[]},{"end":140623055,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140623055,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130723743"},{"seq_region_name":"7","id":"rs1563184080","clinical_significance":[],"start":140623058,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140623058,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs562614808","clinical_significance":[],"end":140623059,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140623059,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1800357643","clinical_significance":[],"strand":1,"feature_type":"variation","end":140623060,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623060,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1415847314","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623061,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140623061},{"clinical_significance":[],"seq_region_name":"7","id":"rs998788566","source":"dbSNP","start":140623064,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140623064,"alleles":["G","A"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623068,"feature_type":"variation","strand":1,"end":140623068,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1165537068"},{"seq_region_name":"7","id":"rs1179957564","clinical_significance":[],"strand":1,"feature_type":"variation","end":140623072,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623072,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140623073,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623073,"clinical_significance":[],"seq_region_name":"7","id":"rs1035900917"},{"start":140623077,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140623077,"alleles":["G","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1800358363","clinical_significance":[]},{"alleles":["C","T"],"end":140623082,"strand":1,"feature_type":"variation","start":140623082,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs572628571","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1233668307","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623088,"feature_type":"variation","strand":1,"end":140623088,"alleles":["A","G"]},{"clinical_significance":[],"id":"rs959905625","seq_region_name":"7","end":140623089,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140623089,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"source":"dbSNP","start":140623091,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140623091,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs548871527","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623094,"feature_type":"variation","strand":1,"end":140623094,"alleles":["G","C"],"clinical_significance":[],"id":"rs1800358852","seq_region_name":"7"},{"alleles":["G","A"],"end":140623097,"strand":1,"feature_type":"variation","start":140623097,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1800358946","clinical_significance":[]},{"id":"rs2130723826","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140623098,"strand":1,"feature_type":"variation","start":140623098,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623099,"source":"dbSNP","strand":1,"feature_type":"variation","end":140623099,"alleles":["C","A"],"id":"rs2130723832","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1014047480","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623100,"feature_type":"variation","strand":1,"end":140623100,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800359174","alleles":["G","A"],"end":140623101,"feature_type":"variation","strand":1,"source":"dbSNP","start":140623101,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["G","A"],"end":140623103,"feature_type":"variation","strand":1,"source":"dbSNP","start":140623103,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1214376076"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623105,"source":"dbSNP","strand":1,"feature_type":"variation","end":140623105,"alleles":["C","T"],"seq_region_name":"7","id":"rs567432411","clinical_significance":[]},{"clinical_significance":[],"id":"rs1023716770","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623106,"feature_type":"variation","strand":1,"end":140623106,"alleles":["G","A"]},{"start":140623107,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140623107,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1311208419","clinical_significance":[]},{"end":140623109,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140623109,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1800360280","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623116,"source":"dbSNP","strand":1,"feature_type":"variation","end":140623116,"alleles":["C","G"],"seq_region_name":"7","id":"rs1585776563","clinical_significance":[]},{"clinical_significance":[],"id":"rs1443913745","seq_region_name":"7","source":"dbSNP","start":140623117,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140623118,"alleles":["CT","-"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623117,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["CTGAACTCAG","-"],"end":140623126,"seq_region_name":"7","id":"rs2130723876","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623118,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140623118,"clinical_significance":[],"seq_region_name":"7","id":"rs1025527283"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623120,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140623120,"id":"rs1374440696","seq_region_name":"7","clinical_significance":[]},{"id":"rs1228210344","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140623121,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623121,"source":"dbSNP"},{"start":140623122,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140623122,"alleles":["C","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1294326194","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1279791111","source":"dbSNP","start":140623123,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140623123,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1448478331","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623124,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G"],"end":140623124},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140623128,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623128,"clinical_significance":[],"id":"rs1800361222","seq_region_name":"7"},{"alleles":["T","G"],"end":140623130,"feature_type":"variation","strand":1,"source":"dbSNP","start":140623130,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130723911"},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140623132,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623132,"clinical_significance":[],"id":"rs1397631795","seq_region_name":"7"},{"id":"rs891029842","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140623133,"alleles":["G","A","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623133,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585776635","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623136,"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140623136},{"source":"dbSNP","start":140623137,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140623137,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1800361651"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623138,"feature_type":"variation","strand":1,"end":140623138,"alleles":["C","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1351613311"},{"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140623141,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623141,"source":"dbSNP","seq_region_name":"7","id":"rs1585776648","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140623145,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623145,"source":"dbSNP","seq_region_name":"7","id":"rs1800361966","clinical_significance":[]},{"seq_region_name":"7","id":"rs2130723960","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623150,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140623150},{"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140623155,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623155,"source":"dbSNP","id":"rs2130723962","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130723968","end":140623156,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140623156,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs528608754","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623160,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140623160},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623161,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140623161,"clinical_significance":[],"seq_region_name":"7","id":"rs1232017408"},{"alleles":["-","CCGTCTCTACT"],"end":140623161,"strand":1,"feature_type":"variation","start":140623162,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130723981","clinical_significance":[]},{"seq_region_name":"7","id":"rs1404564312","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140623174,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623174,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623175,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140623175,"clinical_significance":[],"seq_region_name":"7","id":"rs1408393623"},{"seq_region_name":"7","id":"rs1180245837","clinical_significance":[],"alleles":["G","A","T"],"end":140623176,"strand":1,"feature_type":"variation","start":140623176,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"id":"rs1438119765","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140623178,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623178,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1800362688","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140623179,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623179,"source":"dbSNP"},{"start":140623183,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140623183,"strand":1,"feature_type":"variation","id":"rs1289154574","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs969478147","feature_type":"variation","strand":1,"alleles":["G","A","C"],"end":140623184,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623184},{"seq_region_name":"7","id":"rs1028320435","clinical_significance":[],"start":140623187,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140623187,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140623189,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140623189,"alleles":["C","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs546678535","seq_region_name":"7"},{"clinical_significance":[],"id":"rs984743086","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140623193,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623193},{"seq_region_name":"7","id":"rs181722776","clinical_significance":[],"alleles":["A","G"],"end":140623195,"strand":1,"feature_type":"variation","start":140623195,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"feature_type":"variation","strand":1,"end":140623198,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623198,"clinical_significance":[],"seq_region_name":"7","id":"rs1018106923"},{"alleles":["A","G"],"end":140623204,"feature_type":"variation","strand":1,"source":"dbSNP","start":140623204,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1800363559","seq_region_name":"7"},{"alleles":["T","C"],"end":140623206,"strand":1,"feature_type":"variation","start":140623206,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1800363655","clinical_significance":[]},{"source":"dbSNP","start":140623207,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140623207,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1317927371"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623211,"feature_type":"variation","strand":1,"end":140623211,"alleles":["A","G"],"clinical_significance":[],"id":"rs963885422","seq_region_name":"7"},{"end":140623220,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140623220,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1238396693"},{"seq_region_name":"7","id":"rs538599456","clinical_significance":[],"start":140623226,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140623226,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"alleles":["T","C"],"end":140623228,"strand":1,"feature_type":"variation","start":140623228,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1308071255","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1188328185","feature_type":"variation","strand":1,"end":140623229,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623229},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800364718","alleles":["G","T"],"end":140623230,"feature_type":"variation","strand":1,"source":"dbSNP","start":140623230,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs2130724093","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623231,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140623231},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623232,"feature_type":"variation","strand":1,"end":140623232,"alleles":["T","C"],"clinical_significance":[],"id":"rs972357318","seq_region_name":"7"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623232,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["TTG","TTGTTG"],"end":140623234,"seq_region_name":"7","id":"rs1441007884","clinical_significance":[]},{"seq_region_name":"7","id":"rs1585776834","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G"],"end":140623238,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623238,"source":"dbSNP"},{"strand":1,"feature_type":"variation","end":140623239,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623239,"source":"dbSNP","id":"rs1474144697","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs923400328","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623240,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140623240},{"seq_region_name":"7","id":"rs1800365843","clinical_significance":[],"start":140623244,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140623244,"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623246,"feature_type":"variation","strand":1,"alleles":["C","A"],"end":140623246,"clinical_significance":[],"id":"rs933507101","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1800366099","clinical_significance":[],"start":140623248,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140623248,"strand":1,"feature_type":"variation"},{"alleles":["A","G"],"end":140623249,"strand":1,"feature_type":"variation","start":140623249,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1800366225","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585776865","end":140623251,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140623251,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1345691936","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623252,"source":"dbSNP","strand":1,"feature_type":"variation","end":140623252,"alleles":["T","C","G"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623258,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140623258,"seq_region_name":"7","id":"rs1160298746","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140623259,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623259,"source":"dbSNP","seq_region_name":"7","id":"rs1417631916","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623260,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140623260,"clinical_significance":[],"id":"rs1379926693","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1419593468","alleles":["G","A"],"end":140623261,"feature_type":"variation","strand":1,"source":"dbSNP","start":140623261,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["A","G"],"end":140623264,"feature_type":"variation","strand":1,"source":"dbSNP","start":140623264,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1585776913","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130724162","source":"dbSNP","start":140623267,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140623267,"alleles":["A","T"],"feature_type":"variation","strand":1},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623268,"feature_type":"variation","strand":1,"end":140623268,"alleles":["T","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs550882010"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623270,"source":"dbSNP","strand":1,"feature_type":"variation","end":140623270,"alleles":["A","T"],"id":"rs1800367542","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140623275,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140623275,"alleles":["A","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs2130724178"},{"seq_region_name":"7","id":"rs1051072516","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140623277,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623277,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563184243","alleles":["-","TGT"],"end":140623277,"feature_type":"variation","strand":1,"source":"dbSNP","start":140623278,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623278,"feature_type":"variation","strand":1,"end":140623278,"alleles":["G","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1265306665"},{"source":"dbSNP","start":140623279,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140623279,"alleles":["C","G","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1190651911"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563184251","source":"dbSNP","start":140623279,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140623281,"alleles":["CAC","-"],"feature_type":"variation","strand":1},{"start":140623280,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G","T"],"end":140623280,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1800368289","clinical_significance":[]},{"seq_region_name":"7","id":"rs1800368410","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623281,"source":"dbSNP","strand":1,"feature_type":"variation","end":140623281,"alleles":["C","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585776948","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623282,"feature_type":"variation","strand":1,"end":140623282,"alleles":["T","C"]},{"end":140623283,"alleles":["C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140623283,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1800368627"},{"clinical_significance":[],"id":"rs990209053","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623286,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140623286},{"source":"dbSNP","start":140623288,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140623288,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1800368850"},{"source":"dbSNP","start":140623289,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140623289,"alleles":["T","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1800368942","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800369031","end":140623290,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140623290,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["G","A"],"end":140623291,"strand":1,"feature_type":"variation","start":140623291,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1265954533","clinical_significance":[]},{"id":"rs1214990990","seq_region_name":"7","clinical_significance":[],"end":140623293,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","start":140623293,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1353354881","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623294,"feature_type":"variation","strand":1,"end":140623294,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs377235459","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140623298,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623298,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623299,"source":"dbSNP","strand":1,"feature_type":"variation","end":140623299,"alleles":["A","G"],"id":"rs1284880314","seq_region_name":"7","clinical_significance":[]},{"start":140623301,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140623301,"alleles":["C","A","T"],"strand":1,"feature_type":"variation","id":"rs1167839377","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140623302,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623302,"source":"dbSNP","seq_region_name":"7","id":"rs370822599","clinical_significance":[]},{"start":140623303,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140623303,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1298623894","clinical_significance":[]},{"seq_region_name":"7","id":"rs1385721430","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623309,"source":"dbSNP","strand":1,"feature_type":"variation","end":140623309,"alleles":["T","C"]},{"start":140623310,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140623310,"alleles":["A","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1415044274","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623311,"source":"dbSNP","strand":1,"feature_type":"variation","end":140623311,"alleles":["T","C","G"],"seq_region_name":"7","id":"rs1362660008","clinical_significance":[]},{"alleles":["C","A"],"end":140623312,"feature_type":"variation","strand":1,"source":"dbSNP","start":140623312,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1397934430"},{"end":140623313,"alleles":["T","A","C"],"strand":1,"feature_type":"variation","start":140623313,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1313753296","clinical_significance":[]},{"end":140623313,"alleles":["T","-"],"strand":1,"feature_type":"variation","start":140623313,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1359609592","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140623314,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623314,"source":"dbSNP","id":"rs1376107243","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800370959","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623314,"feature_type":"variation","strand":1,"end":140623315,"alleles":["CC","C"]},{"alleles":["C","A","T"],"end":140623315,"feature_type":"variation","strand":1,"source":"dbSNP","start":140623315,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1440932375"},{"feature_type":"variation","strand":1,"alleles":["CA","-"],"end":140623316,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623315,"clinical_significance":[],"seq_region_name":"7","id":"rs1800371186"},{"strand":1,"feature_type":"variation","alleles":["A","C","G"],"end":140623316,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623316,"source":"dbSNP","seq_region_name":"7","id":"rs1313808538","clinical_significance":[]},{"id":"rs11321461","seq_region_name":"7","clinical_significance":[],"start":140623316,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAA","AAAAAAAAAAAAA","AAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAAAAA"],"end":140623335,"strand":1,"feature_type":"variation"},{"id":"rs1800371908","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140623321,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623321,"source":"dbSNP"},{"id":"rs1357764596","seq_region_name":"7","clinical_significance":[],"start":140623329,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140623329,"alleles":["A","C"],"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","alleles":["-","T"],"end":140623329,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623330,"source":"dbSNP","seq_region_name":"7","id":"rs1253879864","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs910297177","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623331,"feature_type":"variation","strand":1,"end":140623331,"alleles":["A","G"]},{"clinical_significance":[],"id":"rs977815880","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623334,"feature_type":"variation","strand":1,"alleles":["A","G","T"],"end":140623334},{"clinical_significance":[],"id":"rs1800372511","seq_region_name":"7","alleles":["A","T"],"end":140623335,"feature_type":"variation","strand":1,"source":"dbSNP","start":140623335,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1413473269","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140623336,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623336,"source":"dbSNP"},{"alleles":["G","-"],"end":140623336,"strand":1,"feature_type":"variation","start":140623336,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1800372764","clinical_significance":[]},{"end":140623337,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140623337,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1284190681","seq_region_name":"7"},{"seq_region_name":"7","id":"rs947150868","clinical_significance":[],"start":140623339,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140623339,"alleles":["C","T"],"strand":1,"feature_type":"variation"},{"end":140623340,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140623340,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1800373121","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623347,"source":"dbSNP","strand":1,"feature_type":"variation","end":140623347,"alleles":["T","A","C"],"id":"rs969239976","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1042728558","end":140623349,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140623349,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140623351,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140623351,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1313220005","clinical_significance":[]},{"seq_region_name":"7","id":"rs1800373592","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623353,"source":"dbSNP","strand":1,"feature_type":"variation","end":140623353,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs1270995362","clinical_significance":[],"alleles":["G","A"],"end":140623354,"strand":1,"feature_type":"variation","start":140623354,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"end":140623356,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140623356,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1800373815","seq_region_name":"7"},{"clinical_significance":[],"id":"rs928690181","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623357,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140623357},{"end":140623358,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140623358,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs2130724428","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800374049","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623359,"feature_type":"variation","strand":1,"alleles":["-","G"],"end":140623358},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800374157","feature_type":"variation","strand":1,"end":140623359,"alleles":["C","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623359},{"source":"dbSNP","start":140623360,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140623360,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1800374257"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623361,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","C"],"end":140623361,"id":"rs2130724443","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140623362,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623362,"clinical_significance":[],"seq_region_name":"7","id":"rs1800374388"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130724461","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140623363,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623363},{"clinical_significance":[],"seq_region_name":"7","id":"rs1400412968","source":"dbSNP","start":140623366,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140623366,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1302411996","clinical_significance":[],"start":140623369,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140623369,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"end":140623371,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140623371,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130724480"},{"strand":1,"feature_type":"variation","end":140623373,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623373,"source":"dbSNP","seq_region_name":"7","id":"rs1800374727","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs938916252","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623376,"feature_type":"variation","strand":1,"end":140623376,"alleles":["G","A"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623377,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140623377,"seq_region_name":"7","id":"rs1402487122","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623378,"source":"dbSNP","strand":1,"feature_type":"variation","end":140623378,"alleles":["G","A"],"id":"rs1169201625","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","A"],"end":140623383,"feature_type":"variation","strand":1,"source":"dbSNP","start":140623383,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1800375202","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623388,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140623388,"clinical_significance":[],"seq_region_name":"7","id":"rs1800375315"},{"clinical_significance":[],"id":"rs567910117","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623388,"feature_type":"variation","strand":1,"end":140623390,"alleles":["TCT","TCTGAAGTCT"]},{"end":140623391,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140623391,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1419197053"},{"seq_region_name":"7","id":"rs902861459","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623393,"source":"dbSNP","strand":1,"feature_type":"variation","end":140623393,"alleles":["G","A"]},{"start":140623394,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","G"],"end":140623394,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs2130724537","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1422364641","source":"dbSNP","start":140623398,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140623398,"alleles":["G","A","C"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140623400,"alleles":["T","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623400,"source":"dbSNP","seq_region_name":"7","id":"rs1199481663","clinical_significance":[]},{"id":"rs1800375924","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140623402,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623402,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1211869896","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623403,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G","T"],"end":140623403},{"alleles":["G","C"],"end":140623404,"strand":1,"feature_type":"variation","start":140623404,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1294701736","seq_region_name":"7","clinical_significance":[]},{"alleles":["A","G"],"end":140623407,"feature_type":"variation","strand":1,"source":"dbSNP","start":140623407,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1800376238"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623409,"source":"dbSNP","strand":1,"feature_type":"variation","end":140623409,"alleles":["G","A","C"],"seq_region_name":"7","id":"rs1259346036","clinical_significance":[]},{"id":"rs1800376502","seq_region_name":"7","clinical_significance":[],"start":140623412,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140623412,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130724596","source":"dbSNP","start":140623413,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","T"],"end":140623413,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs991732973","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140623415,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623415},{"id":"rs1800376699","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140623417,"alleles":["A","G"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623417,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1196182024","source":"dbSNP","start":140623418,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140623418,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs187395396","clinical_significance":[],"start":140623419,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140623419,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1057049080","alleles":["T","C"],"end":140623420,"feature_type":"variation","strand":1,"source":"dbSNP","start":140623420,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140623427,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140623427,"strand":1,"feature_type":"variation","id":"rs1246721081","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623430,"feature_type":"variation","strand":1,"end":140623430,"alleles":["C","A"],"clinical_significance":[],"id":"rs1338422314","seq_region_name":"7"},{"seq_region_name":"7","id":"rs2130724633","clinical_significance":[],"end":140623437,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140623437,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623439,"source":"dbSNP","strand":1,"feature_type":"variation","end":140623439,"alleles":["C","A","T"],"seq_region_name":"7","id":"rs1800377551","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623440,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140623440,"clinical_significance":[],"seq_region_name":"7","id":"rs895758437"},{"alleles":["T","C"],"end":140623441,"feature_type":"variation","strand":1,"source":"dbSNP","start":140623441,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1800377826"},{"seq_region_name":"7","id":"rs898248263","clinical_significance":[],"start":140623443,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140623443,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1563184400","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623447,"source":"dbSNP","strand":1,"feature_type":"variation","end":140623449,"alleles":["GGG","GGGGG"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800378159","source":"dbSNP","start":140623452,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140623452,"alleles":["G","C"],"feature_type":"variation","strand":1},{"feature_type":"variation","strand":1,"end":140623453,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623453,"clinical_significance":[],"seq_region_name":"7","id":"rs1329459041"},{"seq_region_name":"7","id":"rs191027407","clinical_significance":[],"strand":1,"feature_type":"variation","end":140623455,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623455,"source":"dbSNP"},{"id":"rs1476370657","seq_region_name":"7","clinical_significance":[],"alleles":["C","T"],"end":140623457,"strand":1,"feature_type":"variation","start":140623457,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623458,"source":"dbSNP","strand":1,"feature_type":"variation","end":140623458,"alleles":["G","A","T"],"id":"rs1165449578","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1187167040","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140623463,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623463},{"clinical_significance":[],"seq_region_name":"7","id":"rs1047168728","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140623465,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623465},{"seq_region_name":"7","id":"rs1012744008","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623467,"source":"dbSNP","strand":1,"feature_type":"variation","end":140623467,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1439969208","end":140623468,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140623468,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs573385154","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140623470,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623470,"source":"dbSNP"},{"alleles":["C","T"],"end":140623478,"feature_type":"variation","strand":1,"source":"dbSNP","start":140623478,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs534752618","seq_region_name":"7"},{"seq_region_name":"7","id":"rs905266916","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623486,"source":"dbSNP","strand":1,"feature_type":"variation","end":140623486,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800379511","end":140623488,"alleles":["G","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140623488,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1434880375","alleles":["C","T"],"end":140623495,"feature_type":"variation","strand":1,"source":"dbSNP","start":140623495,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs1006279577","clinical_significance":[],"alleles":["G","A"],"end":140623496,"strand":1,"feature_type":"variation","start":140623496,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1016190633","feature_type":"variation","strand":1,"end":140623498,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623498},{"clinical_significance":[],"seq_region_name":"7","id":"rs28498721","feature_type":"variation","strand":1,"end":140623500,"alleles":["C","G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623500},{"clinical_significance":[],"seq_region_name":"7","id":"rs577717400","source":"dbSNP","start":140623501,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140623501,"alleles":["G","A","C"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623501,"source":"dbSNP","strand":1,"feature_type":"variation","end":140623503,"alleles":["GGG","GG"],"seq_region_name":"7","id":"rs1018221965","clinical_significance":[]},{"alleles":["G","A","C"],"end":140623503,"strand":1,"feature_type":"variation","start":140623503,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs75654105","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623504,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","G","T"],"end":140623504,"seq_region_name":"7","id":"rs78131542","clinical_significance":[]},{"start":140623505,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140623505,"alleles":["A","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1800380577","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1377643816","alleles":["T","C"],"end":140623509,"feature_type":"variation","strand":1,"source":"dbSNP","start":140623509,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623511,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140623511,"seq_region_name":"7","id":"rs544994500","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["-","CT"],"end":140623511,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623512,"source":"dbSNP","seq_region_name":"7","id":"rs1800380860","clinical_significance":[]},{"id":"rs563616425","seq_region_name":"7","clinical_significance":[],"start":140623512,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A","C"],"end":140623512,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800381069","source":"dbSNP","start":140623514,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140623514,"alleles":["G","T"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623515,"source":"dbSNP","strand":1,"feature_type":"variation","end":140623515,"alleles":["G","A"],"seq_region_name":"7","id":"rs1446150878","clinical_significance":[]},{"start":140623522,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140623522,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1800381183","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140623523,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623523,"clinical_significance":[],"seq_region_name":"7","id":"rs1331707431"},{"source":"dbSNP","start":140623525,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","G","T"],"end":140623525,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs899627812"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623526,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140623526,"id":"rs1030582147","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140623531,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A"],"end":140623531,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1011421815"},{"start":140623533,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140623532,"alleles":["-","ACATGGTGAAACCCTG"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1421896248","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800381860","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623533,"feature_type":"variation","strand":1,"end":140623533,"alleles":["G","A"]},{"seq_region_name":"7","id":"rs1800381964","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623534,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140623534},{"feature_type":"variation","strand":1,"alleles":["CC","C"],"end":140623535,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623534,"clinical_significance":[],"id":"rs368723797","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1800382189","clinical_significance":[],"start":140623536,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140623536,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1800382296","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623538,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140623538},{"id":"rs533261245","seq_region_name":"7","clinical_significance":[],"end":140623540,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140623540,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs57021669","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623541,"source":"dbSNP","strand":1,"feature_type":"variation","end":140623541,"alleles":["A","G","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623543,"feature_type":"variation","strand":1,"end":140623543,"alleles":["C","A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1563184504"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1438563079","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623544,"feature_type":"variation","strand":1,"end":140623544,"alleles":["A","G"]},{"source":"dbSNP","start":140623545,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140623545,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1800382950"},{"feature_type":"variation","strand":1,"end":140623547,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623547,"clinical_significance":[],"seq_region_name":"7","id":"rs1246741377"},{"end":140623548,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140623548,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs967862394"},{"id":"rs1585777758","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140623553,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623553,"source":"dbSNP"},{"id":"rs1449853330","seq_region_name":"7","clinical_significance":[],"start":140623554,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140623554,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1364626517","seq_region_name":"7","alleles":["C","T"],"end":140623556,"feature_type":"variation","strand":1,"source":"dbSNP","start":140623556,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140623557,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140623557,"strand":1,"feature_type":"variation","id":"rs376196863","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["A","C"],"end":140623563,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623563,"clinical_significance":[],"seq_region_name":"7","id":"rs1282795734"},{"id":"rs1800383827","seq_region_name":"7","clinical_significance":[],"start":140623564,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140623564,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1745784317","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140623565,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623565},{"clinical_significance":[],"seq_region_name":"7","id":"rs1489116430","feature_type":"variation","strand":1,"end":140623569,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623569},{"feature_type":"variation","strand":1,"alleles":["C","A","G"],"end":140623573,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623573,"clinical_significance":[],"seq_region_name":"7","id":"rs1800384022"},{"source":"dbSNP","start":140623574,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140623574,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1284177409"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623574,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["AAAAA","AAAAAA"],"end":140623578,"id":"rs1800384252","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140623583,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623583,"clinical_significance":[],"seq_region_name":"7","id":"rs1800384358"},{"strand":1,"feature_type":"variation","end":140623589,"alleles":["A","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623589,"source":"dbSNP","seq_region_name":"7","id":"rs1585777859","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140623590,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623590,"source":"dbSNP","id":"rs1036089877","seq_region_name":"7","clinical_significance":[]},{"start":140623592,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140623592,"alleles":["G","A","C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs947088695","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1345946290","alleles":["C","T"],"end":140623596,"feature_type":"variation","strand":1,"source":"dbSNP","start":140623596,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140623597,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623597,"clinical_significance":[],"seq_region_name":"7","id":"rs528229415"},{"end":140623599,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140623599,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1231140149","seq_region_name":"7"},{"id":"rs924232190","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","A","G","T"],"end":140623600,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623600,"source":"dbSNP"},{"alleles":["G","A"],"end":140623601,"strand":1,"feature_type":"variation","start":140623601,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1299269970","clinical_significance":[]},{"id":"rs934339836","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140623606,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623606,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1800385579","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623609,"feature_type":"variation","strand":1,"end":140623609,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800385677","source":"dbSNP","start":140623617,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140623617,"alleles":["A","G"],"feature_type":"variation","strand":1},{"alleles":["C","T"],"end":140623618,"feature_type":"variation","strand":1,"source":"dbSNP","start":140623618,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1585777914"},{"id":"rs1358969017","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623620,"source":"dbSNP","strand":1,"feature_type":"variation","end":140623620,"alleles":["C","T"]},{"source":"dbSNP","start":140623621,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140623621,"alleles":["G","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1284720113"},{"end":140623623,"alleles":["G","T"],"strand":1,"feature_type":"variation","start":140623623,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1800386057","clinical_significance":[]},{"source":"dbSNP","start":140623624,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140623624,"alleles":["A","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs62485845"},{"start":140623625,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140623625,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1190942427","clinical_significance":[]},{"id":"rs1800386384","seq_region_name":"7","clinical_significance":[],"start":140623626,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140623626,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1800386485","clinical_significance":[],"alleles":["G","A"],"end":140623631,"strand":1,"feature_type":"variation","start":140623631,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623636,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140623636,"seq_region_name":"7","id":"rs963481345","clinical_significance":[]},{"end":140623637,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140623637,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585777972","clinical_significance":[]},{"end":140623644,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140623644,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1800386779","seq_region_name":"7"},{"strand":1,"feature_type":"variation","end":140623648,"alleles":["C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623648,"source":"dbSNP","seq_region_name":"7","id":"rs1800386876","clinical_significance":[]},{"alleles":["C","T"],"end":140623650,"feature_type":"variation","strand":1,"source":"dbSNP","start":140623650,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1800386974"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800387081","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140623652,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623652},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623653,"source":"dbSNP","strand":1,"feature_type":"variation","end":140623653,"alleles":["A","G"],"seq_region_name":"7","id":"rs2130725071","clinical_significance":[]},{"start":140623657,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140623657,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1800387186","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs895720136","feature_type":"variation","strand":1,"alleles":["G","T"],"end":140623664,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623664},{"source":"dbSNP","start":140623665,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140623665,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs948668915"},{"seq_region_name":"7","id":"rs1800387449","clinical_significance":[],"start":140623667,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140623667,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"start":140623670,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140623670,"alleles":["G","A"],"strand":1,"feature_type":"variation","id":"rs1800387546","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800387645","source":"dbSNP","start":140623672,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140623672,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1476717564","source":"dbSNP","start":140623673,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140623673,"alleles":["A","G"],"feature_type":"variation","strand":1},{"id":"rs1246879641","seq_region_name":"7","clinical_significance":[],"end":140623676,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140623676,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623677,"source":"dbSNP","strand":1,"feature_type":"variation","end":140623677,"alleles":["G","A"],"seq_region_name":"7","id":"rs1194236872","clinical_significance":[]},{"end":140623680,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140623680,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1489168536"},{"alleles":["T","C"],"end":140623684,"strand":1,"feature_type":"variation","start":140623684,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1260817652","clinical_significance":[]},{"alleles":["C","A"],"end":140623686,"strand":1,"feature_type":"variation","start":140623686,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1800388230","clinical_significance":[]},{"source":"dbSNP","start":140623687,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140623690,"alleles":["CACA","CACACA"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1454383334"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800388539","alleles":["C","T"],"end":140623689,"feature_type":"variation","strand":1,"source":"dbSNP","start":140623689,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"alleles":["G","C"],"end":140623696,"feature_type":"variation","strand":1,"source":"dbSNP","start":140623696,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1800388672"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623697,"feature_type":"variation","strand":1,"end":140623697,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs973972734"},{"seq_region_name":"7","id":"rs1585778036","clinical_significance":[],"alleles":["G","A"],"end":140623699,"strand":1,"feature_type":"variation","start":140623699,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800389150","source":"dbSNP","start":140623700,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["ACA","ACACA"],"end":140623702,"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623701,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140623701,"id":"rs1800389303","seq_region_name":"7","clinical_significance":[]},{"alleles":["G","C"],"end":140623703,"strand":1,"feature_type":"variation","start":140623703,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs147836522","clinical_significance":[]},{"id":"rs1280988661","seq_region_name":"7","clinical_significance":[],"alleles":["G","A"],"end":140623709,"strand":1,"feature_type":"variation","start":140623709,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs532384553","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140623710,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623710,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1800391317","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623711,"feature_type":"variation","strand":1,"end":140623711,"alleles":["C","T"]},{"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140623714,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623714,"source":"dbSNP","seq_region_name":"7","id":"rs1344324397","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1279410060","end":140623715,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140623715,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623718,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A","C"],"end":140623718,"id":"rs1220956675","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs773670750","end":140623719,"alleles":["A","AA","AAA","AAAA","ATAA"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140623719,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623720,"feature_type":"variation","strand":1,"alleles":["-","T"],"end":140623719,"clinical_significance":[],"seq_region_name":"7","id":"rs1800391996"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623720,"source":"dbSNP","strand":1,"feature_type":"variation","end":140623720,"alleles":["G","A","T"],"seq_region_name":"7","id":"rs955849320","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1278018074","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623720,"feature_type":"variation","strand":1,"end":140623720,"alleles":["G","-"]},{"start":140623720,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140623720,"alleles":["G","GG"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1800392193","clinical_significance":[]},{"seq_region_name":"7","id":"rs1554482672","clinical_significance":[],"start":140623721,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["-","GAA"],"end":140623720,"strand":1,"feature_type":"variation"},{"end":140623721,"alleles":["A","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140623721,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1172297695"},{"start":140623721,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AAAAAAAAAAAAAAAA","AAAAAAAAAA","AAAAAAAAAAAA","AAAAAAAAAAAAA","AAAAAAAAAAAAAA","AAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAA","AAAAAAAAAAAAAAAAAAAAA"],"end":140623736,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs34329204","clinical_significance":[]},{"seq_region_name":"7","id":"rs1402945065","clinical_significance":[],"start":140623725,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["-","G"],"end":140623724,"strand":1,"feature_type":"variation"},{"id":"rs1800393432","seq_region_name":"7","clinical_significance":[],"start":140623731,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["-","G"],"end":140623730,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1585778186","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["-","G"],"end":140623732,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623733,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1800393753","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623733,"source":"dbSNP","strand":1,"feature_type":"variation","end":140623734,"alleles":["AA","AATAA"]},{"seq_region_name":"7","id":"rs1466535459","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140623737,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623737,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140623738,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623738,"clinical_significance":[],"seq_region_name":"7","id":"rs1239443280"},{"id":"rs1305756850","seq_region_name":"7","clinical_significance":[],"start":140623740,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A","T"],"end":140623740,"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs929696900","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623747,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140623747},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623750,"feature_type":"variation","strand":1,"end":140623750,"alleles":["G","C"],"clinical_significance":[],"seq_region_name":"7","id":"rs1800394557"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623751,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","C"],"end":140623751,"seq_region_name":"7","id":"rs1044185493","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623753,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140623753,"clinical_significance":[],"seq_region_name":"7","id":"rs1800394770"},{"feature_type":"variation","strand":1,"end":140623755,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623755,"clinical_significance":[],"seq_region_name":"7","id":"rs74897731"},{"feature_type":"variation","strand":1,"end":140623756,"alleles":["C","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623756,"clinical_significance":[],"seq_region_name":"7","id":"rs533116205"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800395116","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623757,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140623757},{"source":"dbSNP","start":140623761,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140623761,"alleles":["G","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1257904528"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1229263344","source":"dbSNP","start":140623765,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","C"],"end":140623765,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1006228836","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623766,"feature_type":"variation","strand":1,"alleles":["A","T"],"end":140623766},{"start":140623768,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140623768,"alleles":["C","G"],"strand":1,"feature_type":"variation","id":"rs1285627497","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800395653","source":"dbSNP","start":140623769,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["TGCTGAACCCTT","-"],"end":140623780,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1800395731","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623772,"source":"dbSNP","strand":1,"feature_type":"variation","end":140623772,"alleles":["T","C"]},{"id":"rs1445414878","seq_region_name":"7","clinical_significance":[],"start":140623773,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140623773,"alleles":["G","A"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623776,"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140623776,"clinical_significance":[],"id":"rs1800395899","seq_region_name":"7"},{"alleles":["T","C"],"end":140623779,"feature_type":"variation","strand":1,"source":"dbSNP","start":140623779,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1381560751"},{"end":140623782,"alleles":["A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140623782,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs2130725320"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130725326","end":140623790,"alleles":["T","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140623790,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140623793,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140623793,"alleles":["G","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1016306768","clinical_significance":[]},{"source":"dbSNP","start":140623794,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140623794,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1352656522","seq_region_name":"7"},{"end":140623795,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140623795,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1800396287","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs912207913","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623797,"feature_type":"variation","strand":1,"alleles":["C","G"],"end":140623797},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623798,"feature_type":"variation","strand":1,"end":140623798,"alleles":["A","G"],"clinical_significance":[],"seq_region_name":"7","id":"rs1800396496"},{"seq_region_name":"7","id":"rs1800396610","clinical_significance":[],"end":140623800,"alleles":["T","C","G"],"strand":1,"feature_type":"variation","start":140623800,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1800396733","clinical_significance":[],"alleles":["A","G"],"end":140623804,"strand":1,"feature_type":"variation","start":140623804,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["G","A"],"end":140623808,"strand":1,"feature_type":"variation","start":140623808,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs943687601","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800396909","feature_type":"variation","strand":1,"alleles":["G","A"],"end":140623809,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623809},{"end":140623813,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140623813,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1563184723","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800397205","feature_type":"variation","strand":1,"alleles":["T","C"],"end":140623818,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623818},{"clinical_significance":[],"id":"rs1468516697","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","T"],"end":140623821,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623821},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623827,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140623827,"seq_region_name":"7","id":"rs1398026966","clinical_significance":[]},{"end":140623828,"alleles":["G","A","T"],"strand":1,"feature_type":"variation","start":140623828,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs750240489","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"end":140623830,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623830,"clinical_significance":[],"seq_region_name":"7","id":"rs1800397781"},{"end":140623834,"alleles":["T","C","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140623834,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1415639912","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623838,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140623838,"clinical_significance":[],"seq_region_name":"7","id":"rs569215835"},{"start":140623847,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140623847,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585778412","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1250609494","feature_type":"variation","strand":1,"end":140623852,"alleles":["A","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623852},{"feature_type":"variation","strand":1,"end":140623853,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623853,"clinical_significance":[],"seq_region_name":"7","id":"rs1239006747"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800398443","source":"dbSNP","start":140623856,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","G"],"end":140623856,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1180661308","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623858,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140623858},{"seq_region_name":"7","id":"rs1232835340","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623861,"source":"dbSNP","strand":1,"feature_type":"variation","end":140623866,"alleles":["AAAAAA","AAAAA","AAAAAAA"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623867,"feature_type":"variation","strand":1,"end":140623867,"alleles":["C","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1800398899"},{"clinical_significance":[],"id":"rs899742233","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623875,"feature_type":"variation","strand":1,"end":140623875,"alleles":["T","C"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623876,"feature_type":"variation","strand":1,"end":140623876,"alleles":["T","C"],"clinical_significance":[],"id":"rs993505826","seq_region_name":"7"},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140623878,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623878,"clinical_significance":[],"seq_region_name":"7","id":"rs1182159439"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800399536","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623880,"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140623880},{"seq_region_name":"7","id":"rs2130725456","clinical_significance":[],"end":140623887,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140623887,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1800399705","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["G","C"],"end":140623888,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623888},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623891,"source":"dbSNP","strand":1,"feature_type":"variation","end":140623891,"alleles":["G","A"],"seq_region_name":"7","id":"rs1030778290","clinical_significance":[]},{"seq_region_name":"7","id":"rs1800400049","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140623892,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623892,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1800400214","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623897,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140623897},{"seq_region_name":"7","id":"rs1800400394","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623901,"source":"dbSNP","strand":1,"feature_type":"variation","end":140623901,"alleles":["T","C"]},{"feature_type":"variation","strand":1,"end":140623903,"alleles":["T","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623903,"clinical_significance":[],"seq_region_name":"7","id":"rs1800400531"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800400632","feature_type":"variation","strand":1,"end":140623906,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623906},{"clinical_significance":[],"seq_region_name":"7","id":"rs954967899","alleles":["G","A","T"],"end":140623909,"feature_type":"variation","strand":1,"source":"dbSNP","start":140623909,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623916,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140623916,"seq_region_name":"7","id":"rs903042742","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140623925,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623925,"clinical_significance":[],"id":"rs1800400999","seq_region_name":"7"},{"alleles":["G","A"],"end":140623930,"strand":1,"feature_type":"variation","start":140623930,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1800401099","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["G","A","T"],"end":140623931,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623931,"source":"dbSNP","seq_region_name":"7","id":"rs986808719","clinical_significance":[]},{"seq_region_name":"7","id":"rs374438671","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623932,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140623932},{"clinical_significance":[],"id":"rs1373947102","seq_region_name":"7","end":140623933,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140623933,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585778530","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140623940,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623940},{"clinical_significance":[],"id":"rs1297568096","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623944,"feature_type":"variation","strand":1,"end":140623944,"alleles":["A","C","G","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563184797","feature_type":"variation","strand":1,"end":140623945,"alleles":["G","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623945},{"seq_region_name":"7","id":"rs1437154086","clinical_significance":[],"alleles":["TTCTT","TT"],"end":140623950,"strand":1,"feature_type":"variation","start":140623946,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs149384145","clinical_significance":[],"strand":1,"feature_type":"variation","end":140623954,"alleles":["TTT","TT"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623952,"source":"dbSNP"},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140623953,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140623953,"source":"dbSNP","seq_region_name":"7","id":"rs1162498330","clinical_significance":[]},{"source":"dbSNP","start":140623959,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140623959,"alleles":["C","G"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1800402813"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800402995","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623962,"feature_type":"variation","strand":1,"end":140623962,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1423762028","source":"dbSNP","start":140623963,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140623963,"alleles":["A","G"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1381166696","alleles":["A","G","T"],"end":140623964,"feature_type":"variation","strand":1,"source":"dbSNP","start":140623964,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs1800403524","seq_region_name":"7","clinical_significance":[],"start":140623969,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140623969,"alleles":["G","T"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1437939557","source":"dbSNP","start":140623982,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140623982,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1800403851","clinical_significance":[],"alleles":["A","G"],"end":140623985,"strand":1,"feature_type":"variation","start":140623985,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140623986,"feature_type":"variation","strand":1,"end":140623986,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1800404017"},{"seq_region_name":"7","id":"rs866686102","clinical_significance":[],"start":140623991,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","T"],"end":140623991,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs2130725607","clinical_significance":[],"start":140623992,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140623992,"alleles":["T","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs968875929","clinical_significance":[],"end":140624000,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140624000,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs2130725622","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140624001,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140624001},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624007,"feature_type":"variation","strand":1,"end":140624007,"alleles":["C","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1191824795"},{"seq_region_name":"7","id":"rs1800404722","clinical_significance":[],"alleles":["G","A"],"end":140624008,"strand":1,"feature_type":"variation","start":140624008,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"strand":1,"feature_type":"variation","end":140624009,"alleles":["C","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140624009,"source":"dbSNP","seq_region_name":"7","id":"rs1327943631","clinical_significance":[]},{"seq_region_name":"7","id":"rs1800404975","clinical_significance":[],"start":140624009,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["CCCC","CCC"],"end":140624012,"strand":1,"feature_type":"variation"},{"end":140624012,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140624012,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs141418089","clinical_significance":[]},{"seq_region_name":"7","id":"rs1386421847","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140624013,"source":"dbSNP","strand":1,"feature_type":"variation","end":140624013,"alleles":["G","A","T"]},{"clinical_significance":[],"id":"rs2130725658","seq_region_name":"7","feature_type":"variation","strand":1,"end":140624014,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624014},{"start":140624015,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140624015,"alleles":["C","A"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1488786046","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140624017,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624017,"clinical_significance":[],"seq_region_name":"7","id":"rs1286310061"},{"clinical_significance":[],"id":"rs1800405537","seq_region_name":"7","source":"dbSNP","start":140624019,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140624019,"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800405654","source":"dbSNP","start":140624020,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140624020,"alleles":["C","T"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs924348083","clinical_significance":[],"strand":1,"feature_type":"variation","end":140624021,"alleles":["C","A","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140624021,"source":"dbSNP"},{"clinical_significance":[],"id":"rs269232","seq_region_name":"7","end":140624022,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140624022,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140624023,"source":"dbSNP","strand":1,"feature_type":"variation","end":140624023,"alleles":["T","C"],"id":"rs1800406279","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624026,"feature_type":"variation","strand":1,"end":140624026,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1800406376"},{"seq_region_name":"7","id":"rs534343703","clinical_significance":[],"strand":1,"feature_type":"variation","end":140624028,"alleles":["G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140624028,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140624032,"source":"dbSNP","strand":1,"feature_type":"variation","end":140624032,"alleles":["G","T"],"seq_region_name":"7","id":"rs1800406574","clinical_significance":[]},{"seq_region_name":"7","id":"rs1800406679","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["AAAAA","AAAA"],"end":140624037,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140624033,"source":"dbSNP"},{"feature_type":"variation","strand":1,"end":140624039,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624039,"clinical_significance":[],"seq_region_name":"7","id":"rs1800406783"},{"source":"dbSNP","start":140624040,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140624040,"alleles":["T","C"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1219289677"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130725728","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624042,"feature_type":"variation","strand":1,"end":140624042,"alleles":["T","C"]},{"clinical_significance":[],"id":"rs973705006","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624044,"feature_type":"variation","strand":1,"end":140624044,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1291644852","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624045,"feature_type":"variation","strand":1,"end":140624045,"alleles":["G","A"]},{"clinical_significance":[],"id":"rs1404132982","seq_region_name":"7","feature_type":"variation","strand":1,"end":140624054,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624054},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624056,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140624056,"clinical_significance":[],"seq_region_name":"7","id":"rs916919534"},{"seq_region_name":"7","id":"rs950932242","clinical_significance":[],"end":140624059,"alleles":["T","G"],"strand":1,"feature_type":"variation","start":140624059,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1418156744","clinical_significance":[],"end":140624061,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140624061,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs370280746","seq_region_name":"7","source":"dbSNP","start":140624062,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140624062,"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs912321585","clinical_significance":[],"strand":1,"feature_type":"variation","end":140624063,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140624063,"source":"dbSNP"},{"id":"rs943802292","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140624065,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","A"],"end":140624065},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140624066,"source":"dbSNP","strand":1,"feature_type":"variation","end":140624066,"alleles":["G","T"],"seq_region_name":"7","id":"rs1423697423","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["AGAAG","AG"],"end":140624074,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140624070,"source":"dbSNP","id":"rs1800408152","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1800408280","clinical_significance":[],"end":140624071,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140624071,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1563184889","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","C"],"end":140624073,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140624073,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1199262334","clinical_significance":[],"start":140624073,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AGGAGGAG","AGGAG"],"end":140624080,"strand":1,"feature_type":"variation"},{"strand":1,"feature_type":"variation","end":140624074,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140624074,"source":"dbSNP","id":"rs1478369477","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1265842542","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624077,"feature_type":"variation","strand":1,"end":140624077,"alleles":["G","A"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563184897","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624078,"feature_type":"variation","strand":1,"end":140624078,"alleles":["G","T"]},{"start":140624080,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140624080,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1039382627","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624081,"feature_type":"variation","strand":1,"end":140624081,"alleles":["C","A","T"],"clinical_significance":[],"id":"rs1044299196","seq_region_name":"7"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624085,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140624085,"clinical_significance":[],"seq_region_name":"7","id":"rs1800409247"},{"strand":1,"feature_type":"variation","end":140624090,"alleles":["C","G","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140624090,"source":"dbSNP","seq_region_name":"7","id":"rs143622706","clinical_significance":[]},{"clinical_significance":[],"id":"rs1487904682","seq_region_name":"7","source":"dbSNP","start":140624091,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140624091,"alleles":["A","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1484721418","feature_type":"variation","strand":1,"end":140624093,"alleles":["G","A","C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624093},{"end":140624094,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140624094,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs888241932","clinical_significance":[]},{"end":140624097,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140624097,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs920953003"},{"seq_region_name":"7","id":"rs2130725846","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140624099,"source":"dbSNP","strand":1,"feature_type":"variation","end":140624099,"alleles":["T","C"]},{"clinical_significance":[],"id":"rs947276451","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624108,"feature_type":"variation","strand":1,"end":140624108,"alleles":["C","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140624109,"source":"dbSNP","strand":1,"feature_type":"variation","end":140624109,"alleles":["G","A","C"],"id":"rs1313389795","seq_region_name":"7","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["C","T"],"end":140624113,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624113,"clinical_significance":[],"seq_region_name":"7","id":"rs1800410056"},{"feature_type":"variation","strand":1,"end":140624117,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624117,"clinical_significance":[],"id":"rs1800410176","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1281336353","alleles":["T","C"],"end":140624118,"feature_type":"variation","strand":1,"source":"dbSNP","start":140624118,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140624128,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140624128,"alleles":["T","-"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1800410390","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130725873","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624128,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140624128},{"id":"rs1800410490","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","C"],"end":140624129,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140624129,"source":"dbSNP"},{"seq_region_name":"7","id":"rs941196465","clinical_significance":[],"start":140624139,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140624139,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140624140,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AGAG","AG"],"end":140624143,"feature_type":"variation","strand":1,"clinical_significance":[],"id":"rs1195994150","seq_region_name":"7"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1185155913","feature_type":"variation","strand":1,"end":140624141,"alleles":["G","C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624141},{"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140624147,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140624147,"source":"dbSNP","seq_region_name":"7","id":"rs1042994878","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1341031007","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624149,"feature_type":"variation","strand":1,"end":140624149,"alleles":["T","C","G"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs753523403","feature_type":"variation","strand":1,"end":140624156,"alleles":["A","G"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624156},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800411293","source":"dbSNP","start":140624157,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140624157,"alleles":["G","A"],"feature_type":"variation","strand":1},{"strand":1,"feature_type":"variation","end":140624163,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140624163,"source":"dbSNP","seq_region_name":"7","id":"rs1279925642","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs148065031","source":"dbSNP","start":140624166,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140624166,"alleles":["G","A"],"feature_type":"variation","strand":1},{"clinical_significance":[],"seq_region_name":"7","id":"rs1384536149","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624171,"feature_type":"variation","strand":1,"end":140624171,"alleles":["C","T"]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140624177,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140624177,"seq_region_name":"7","id":"rs1800411709","clinical_significance":[]},{"start":140624184,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140624184,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1303589986","clinical_significance":[]},{"seq_region_name":"7","id":"rs749236992","clinical_significance":[],"end":140624189,"alleles":["T","C"],"strand":1,"feature_type":"variation","start":140624189,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs998703269","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624192,"feature_type":"variation","strand":1,"end":140624192,"alleles":["G","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1357455943","source":"dbSNP","start":140624196,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["T","C"],"end":140624196,"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1800412235","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624197,"feature_type":"variation","strand":1,"alleles":["GA","-"],"end":140624198},{"alleles":["C","T"],"end":140624199,"strand":1,"feature_type":"variation","start":140624199,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1057111223","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1800412439","seq_region_name":"7","source":"dbSNP","start":140624200,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140624199,"alleles":["-","CTGT"],"feature_type":"variation","strand":1},{"seq_region_name":"7","id":"rs1466645620","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140624200,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140624200,"source":"dbSNP"},{"alleles":["C","A"],"end":140624201,"strand":1,"feature_type":"variation","start":140624201,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs540559195","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624202,"feature_type":"variation","strand":1,"end":140624201,"alleles":["-","TGG"],"clinical_significance":[],"seq_region_name":"7","id":"rs1800412790"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800412894","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624203,"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140624203},{"clinical_significance":[],"seq_region_name":"7","id":"rs758587716","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624204,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140624204},{"strand":1,"feature_type":"variation","alleles":["G","T"],"end":140624206,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140624206,"source":"dbSNP","seq_region_name":"7","id":"rs1192033003","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["T","C"],"end":140624208,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624208,"clinical_significance":[],"seq_region_name":"7","id":"rs1800413367"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1428219676","feature_type":"variation","strand":1,"end":140624209,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624209},{"end":140624214,"alleles":["A","C"],"strand":1,"feature_type":"variation","start":140624214,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1585779019","clinical_significance":[]},{"seq_region_name":"7","id":"rs1012995203","clinical_significance":[],"alleles":["C","G","T"],"end":140624220,"strand":1,"feature_type":"variation","start":140624220,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1036860198","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","T"],"end":140624227,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140624227,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1800414222","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140624228,"source":"dbSNP","strand":1,"feature_type":"variation","end":140624228,"alleles":["A","G"]},{"seq_region_name":"7","id":"rs1800414381","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","A"],"end":140624232,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140624232,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140624237,"source":"dbSNP","strand":1,"feature_type":"variation","end":140624237,"alleles":["C","T"],"seq_region_name":"7","id":"rs1260762782","clinical_significance":[]},{"id":"rs1800414684","seq_region_name":"7","clinical_significance":[],"strand":1,"feature_type":"variation","end":140624239,"alleles":["G","A"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140624239,"source":"dbSNP"},{"id":"rs897898535","seq_region_name":"7","clinical_significance":[],"start":140624240,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","C"],"end":140624240,"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1800414978","clinical_significance":[],"start":140624243,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140624243,"alleles":["T","A"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs994014741","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624249,"feature_type":"variation","strand":1,"alleles":["G","A","T"],"end":140624249},{"feature_type":"variation","strand":1,"end":140624250,"alleles":["C","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624250,"clinical_significance":[],"seq_region_name":"7","id":"rs1202472696"},{"strand":1,"feature_type":"variation","end":140624251,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140624251,"source":"dbSNP","seq_region_name":"7","id":"rs1051747300","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","A"],"end":140624252,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140624252,"source":"dbSNP","id":"rs1259841722","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140624255,"source":"dbSNP","strand":1,"feature_type":"variation","end":140624255,"alleles":["C","T"],"seq_region_name":"7","id":"rs1800415800","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130726055","feature_type":"variation","strand":1,"end":140624264,"alleles":["T","C"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624264},{"seq_region_name":"7","id":"rs756693578","clinical_significance":[],"alleles":["C","T"],"end":140624265,"strand":1,"feature_type":"variation","start":140624265,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1800416124","seq_region_name":"7","end":140624268,"alleles":["G","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140624268,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1366782788","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624269,"feature_type":"variation","strand":1,"end":140624269,"alleles":["T","C"]},{"source":"dbSNP","start":140624273,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140624273,"alleles":["T","A"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1313738057"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1325582455","source":"dbSNP","start":140624273,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140624274,"alleles":["TT","TTT"],"feature_type":"variation","strand":1},{"start":140624277,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140624277,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1398044814","clinical_significance":[]},{"source":"dbSNP","start":140624280,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["G","A"],"end":140624280,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1377218838"},{"alleles":["A","C","G"],"end":140624282,"strand":1,"feature_type":"variation","start":140624282,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1457516315","clinical_significance":[]},{"strand":1,"feature_type":"variation","end":140624296,"alleles":["T","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140624296,"source":"dbSNP","id":"rs866125087","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs1403090521","seq_region_name":"7","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624300,"feature_type":"variation","strand":1,"alleles":["A","G"],"end":140624300},{"seq_region_name":"7","id":"rs1800417574","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140624302,"source":"dbSNP","strand":1,"feature_type":"variation","end":140624302,"alleles":["T","C"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800417731","source":"dbSNP","start":140624303,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140624303,"alleles":["G","A"],"feature_type":"variation","strand":1},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140624307,"source":"dbSNP","strand":1,"feature_type":"variation","end":140624307,"alleles":["C","T"],"id":"rs1169091959","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1007773617","feature_type":"variation","strand":1,"alleles":["T","G"],"end":140624308,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624308},{"clinical_significance":[],"id":"rs1563185014","seq_region_name":"7","alleles":["C","T"],"end":140624317,"feature_type":"variation","strand":1,"source":"dbSNP","start":140624317,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"start":140624323,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140624323,"alleles":["T","C"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1369448582","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624324,"feature_type":"variation","strand":1,"end":140624324,"alleles":["A","T"],"clinical_significance":[],"seq_region_name":"7","id":"rs1167321622"},{"clinical_significance":[],"seq_region_name":"7","id":"rs2130726139","source":"dbSNP","start":140624325,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140624325,"alleles":["G","C"],"feature_type":"variation","strand":1},{"clinical_significance":[],"id":"rs1585779197","seq_region_name":"7","feature_type":"variation","strand":1,"end":140624327,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624327},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140624329,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624329,"clinical_significance":[],"seq_region_name":"7","id":"rs1800418672"},{"feature_type":"variation","strand":1,"alleles":["T","A"],"end":140624334,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624334,"clinical_significance":[],"seq_region_name":"7","id":"rs1017866317"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140624337,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140624337,"seq_region_name":"7","id":"rs1240882999","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1398861753","alleles":["A","G"],"end":140624338,"feature_type":"variation","strand":1,"source":"dbSNP","start":140624338,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs995474769","clinical_significance":[],"start":140624342,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140624342,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"clinical_significance":[],"id":"rs1800419507","seq_region_name":"7","end":140624346,"alleles":["A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140624346,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"id":"rs535121792","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140624352,"source":"dbSNP","strand":1,"feature_type":"variation","end":140624367,"alleles":["AACAACAACAACAACA","AACAACAACAACA","AACAACAACAACAACAACA"]},{"start":140624352,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["AACAACAACAACAACACAACAACAACAACAACA","AACAACAACAACAACA"],"end":140624384,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1239971721","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["AACAACAACAACAACACAACAACAACAACAACAA","AACAACAACAACAACACAACAACAACAACAACAACACAACAACAACAACAACAA"],"end":140624385,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624352,"clinical_significance":[],"seq_region_name":"7","id":"rs1800420135"},{"strand":1,"feature_type":"variation","alleles":["ACAACAACAACAACACAACAACAACAACA","ACAACAACAACAACA"],"end":140624381,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140624353,"source":"dbSNP","id":"rs1800420307","seq_region_name":"7","clinical_significance":[]},{"source":"dbSNP","start":140624354,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["C","A","T"],"end":140624354,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1408260253"},{"seq_region_name":"7","id":"rs1585779252","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140624356,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140624356},{"clinical_significance":[],"seq_region_name":"7","id":"rs1193958995","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624356,"feature_type":"variation","strand":1,"end":140624378,"alleles":["ACAACAACAACACAACAACAACA","ACAACAACAACA"]},{"alleles":["C","G","T"],"end":140624357,"strand":1,"feature_type":"variation","start":140624357,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs987648563","seq_region_name":"7","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140624362,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140624362,"source":"dbSNP","id":"rs1307104840","seq_region_name":"7","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140624363,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140624363,"seq_region_name":"7","id":"rs1800421417","clinical_significance":[]},{"alleles":["A","C"],"end":140624365,"strand":1,"feature_type":"variation","start":140624365,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1800421558","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs1019162217","feature_type":"variation","strand":1,"end":140624369,"alleles":["ACACA","ACA"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624365},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800421908","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624365,"feature_type":"variation","strand":1,"alleles":["ACACAACA","A"],"end":140624372},{"feature_type":"variation","strand":1,"end":140624375,"alleles":["ACACAACAACA","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624365,"clinical_significance":[],"seq_region_name":"7","id":"rs1246696493"},{"strand":1,"feature_type":"variation","alleles":["CAC","-"],"end":140624368,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140624366,"source":"dbSNP","id":"rs1800422260","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs1800422435","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","AAA","AAACAA"],"end":140624367,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140624367,"source":"dbSNP"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624367,"feature_type":"variation","strand":1,"alleles":["ACAACAA","-"],"end":140624373,"clinical_significance":[],"seq_region_name":"7","id":"rs751427783"},{"clinical_significance":[],"seq_region_name":"7","id":"rs555315948","feature_type":"variation","strand":1,"alleles":["ACAACAACAACAACAACAA","ACAACAACAACAACAA","ACAACAACAACAACAACAACAA","ACAACAACAACAACAACAACAACAA"],"end":140624385,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624367},{"clinical_significance":[],"seq_region_name":"7","id":"rs200127099","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624368,"feature_type":"variation","strand":1,"end":140624368,"alleles":["C","A","T"]},{"feature_type":"variation","strand":1,"alleles":["C","-"],"end":140624368,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624368,"clinical_significance":[],"id":"rs1447628832","seq_region_name":"7"},{"seq_region_name":"7","id":"rs772062683","clinical_significance":[],"alleles":["CA","CACCA"],"end":140624369,"strand":1,"feature_type":"variation","start":140624368,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"seq_region_name":"7","id":"rs140762832","alleles":["CAACAAC","-"],"end":140624374,"feature_type":"variation","strand":1,"source":"dbSNP","start":140624368,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"seq_region_name":"7","id":"rs753076390","clinical_significance":[],"alleles":["CAACAAC","CAACAACCAACAAC"],"end":140624374,"strand":1,"feature_type":"variation","start":140624368,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1310543535","clinical_significance":[],"start":140624369,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","G"],"end":140624369,"strand":1,"feature_type":"variation"},{"id":"rs1800424529","seq_region_name":"7","clinical_significance":[],"alleles":["AACAACAA","A"],"end":140624376,"strand":1,"feature_type":"variation","start":140624369,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"alleles":["A","G"],"end":140624370,"feature_type":"variation","strand":1,"source":"dbSNP","start":140624370,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1800424697"},{"seq_region_name":"7","id":"rs1800424855","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140624370,"source":"dbSNP","strand":1,"feature_type":"variation","end":140624381,"alleles":["ACAACAACAACA","ACAACAACAACACAACAACAACA"]},{"seq_region_name":"7","id":"rs1800425010","clinical_significance":[],"start":140624371,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140624374,"alleles":["CAAC","-"],"strand":1,"feature_type":"variation"},{"id":"rs1800425178","seq_region_name":"7","clinical_significance":[],"start":140624372,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["A","C"],"end":140624372,"strand":1,"feature_type":"variation"},{"end":140624375,"alleles":["ACA","A"],"strand":1,"feature_type":"variation","start":140624373,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1491047938","seq_region_name":"7","clinical_significance":[]},{"seq_region_name":"7","id":"rs869236461","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["C","-"],"end":140624374,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140624374,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1585779322","clinical_significance":[],"start":140624374,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","A"],"end":140624374,"strand":1,"feature_type":"variation"},{"source":"dbSNP","start":140624375,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["AA","AAA"],"end":140624376,"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1391371865"},{"clinical_significance":[],"id":"rs1800425660","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["AACAA","AACAAACAA"],"end":140624379,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624375},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140624377,"source":"dbSNP","strand":1,"feature_type":"variation","end":140624377,"alleles":["C","G","T"],"seq_region_name":"7","id":"rs1000350846","clinical_significance":[]},{"seq_region_name":"7","id":"rs1392064844","clinical_significance":[],"start":140624378,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140624378,"alleles":["A","G"],"strand":1,"feature_type":"variation"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624388,"feature_type":"variation","strand":1,"end":140624389,"alleles":["TT","-"],"clinical_significance":[],"seq_region_name":"7","id":"rs1171843360"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624389,"feature_type":"variation","strand":1,"alleles":["TAAT","T"],"end":140624392,"clinical_significance":[],"id":"rs1800426315","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1456649353","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["T","C"],"end":140624392,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140624392,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800426620","source":"dbSNP","start":140624393,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140624393,"alleles":["G","A"],"feature_type":"variation","strand":1},{"source":"dbSNP","start":140624397,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140624397,"alleles":["C","T"],"feature_type":"variation","strand":1,"clinical_significance":[],"seq_region_name":"7","id":"rs1032280295"},{"seq_region_name":"7","id":"rs1800426928","clinical_significance":[],"start":140624398,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["T","C"],"end":140624398,"strand":1,"feature_type":"variation"},{"end":140624405,"alleles":["G","A"],"strand":1,"feature_type":"variation","start":140624405,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs556728711","clinical_significance":[]},{"strand":1,"feature_type":"variation","alleles":["C","A","T"],"end":140624406,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140624406,"source":"dbSNP","id":"rs575167196","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"id":"rs373645564","seq_region_name":"7","end":140624407,"alleles":["G","A","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140624407,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1179023191","source":"dbSNP","start":140624409,"consequence_type":"intron_variant","assembly_name":"GRCh38","end":140624409,"alleles":["C","T"],"feature_type":"variation","strand":1},{"id":"rs1800427555","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140624413,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140624413},{"seq_region_name":"7","id":"rs2130726439","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140624416,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","G"],"end":140624416},{"seq_region_name":"7","id":"rs1800427650","clinical_significance":[],"strand":1,"feature_type":"variation","end":140624417,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140624417,"source":"dbSNP"},{"clinical_significance":[],"seq_region_name":"7","id":"rs764739906","end":140624419,"alleles":["G","A","C"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140624419,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140624421,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624421,"clinical_significance":[],"seq_region_name":"7","id":"rs992999741"},{"alleles":["C","T"],"end":140624424,"feature_type":"variation","strand":1,"source":"dbSNP","start":140624424,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs561828356"},{"seq_region_name":"7","id":"rs1800428113","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["A","G"],"end":140624430,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140624430,"source":"dbSNP"},{"seq_region_name":"7","id":"rs1800428197","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140624431,"source":"dbSNP","strand":1,"feature_type":"variation","end":140624431,"alleles":["C","T"]},{"clinical_significance":[],"seq_region_name":"7","id":"rs924561042","end":140624440,"alleles":["A","G"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140624440,"consequence_type":"intron_variant","assembly_name":"GRCh38"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800428404","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624441,"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140624441},{"start":140624443,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140624443,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1800428542","clinical_significance":[]},{"clinical_significance":[],"id":"rs1800428688","seq_region_name":"7","source":"dbSNP","start":140624448,"consequence_type":"intron_variant","assembly_name":"GRCh38","alleles":["A","G"],"end":140624448,"feature_type":"variation","strand":1},{"end":140624451,"alleles":["A","G"],"strand":1,"feature_type":"variation","start":140624451,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","id":"rs1204008726","seq_region_name":"7","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624452,"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140624452,"clinical_significance":[],"seq_region_name":"7","id":"rs1800429024"},{"seq_region_name":"7","id":"rs970131339","clinical_significance":[],"start":140624454,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140624454,"alleles":["T","G"],"strand":1,"feature_type":"variation"},{"start":140624455,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140624455,"strand":1,"feature_type":"variation","id":"rs1800429354","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs561188790","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624459,"feature_type":"variation","strand":1,"end":140624459,"alleles":["C","T"]},{"seq_region_name":"7","id":"rs1241200881","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["CGC","C"],"end":140624461,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140624459,"source":"dbSNP"},{"seq_region_name":"7","id":"rs572721511","clinical_significance":[],"strand":1,"feature_type":"variation","end":140624460,"alleles":["G","A","C","T"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140624460,"source":"dbSNP"},{"feature_type":"variation","strand":1,"alleles":["G","C"],"end":140624466,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624466,"clinical_significance":[],"seq_region_name":"7","id":"rs1800430115"},{"id":"rs2130726548","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140624467,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","T"],"end":140624467},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140624468,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["T","G"],"end":140624468,"seq_region_name":"7","id":"rs2130726554","clinical_significance":[]},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140624469,"source":"dbSNP","strand":1,"feature_type":"variation","end":140624469,"alleles":["G","A"],"seq_region_name":"7","id":"rs750881535","clinical_significance":[]},{"end":140624470,"alleles":["C","T"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140624470,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"id":"rs1403511243","seq_region_name":"7"},{"seq_region_name":"7","id":"rs1800430621","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140624471,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["A","C"],"end":140624471},{"clinical_significance":[],"seq_region_name":"7","id":"rs1800430772","feature_type":"variation","strand":1,"end":140624472,"alleles":["G","T"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624472},{"seq_region_name":"7","id":"rs1800430924","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140624473,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140624473},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140624477,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["C","A"],"end":140624477,"id":"rs1563185153","seq_region_name":"7","clinical_significance":[]},{"clinical_significance":[],"seq_region_name":"7","id":"rs35994844","feature_type":"variation","strand":1,"alleles":["A","C","G"],"end":140624481,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624481},{"end":140624483,"alleles":["T","A","G"],"strand":1,"feature_type":"variation","start":140624483,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","seq_region_name":"7","id":"rs1800431443","clinical_significance":[]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624484,"feature_type":"variation","strand":1,"end":140624484,"alleles":["G","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1365294179"},{"seq_region_name":"7","id":"rs1800431820","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140624486,"source":"dbSNP","strand":1,"feature_type":"variation","alleles":["G","A"],"end":140624486},{"alleles":["C","T"],"end":140624488,"feature_type":"variation","strand":1,"source":"dbSNP","start":140624488,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1299158385"},{"seq_region_name":"7","id":"rs1800432170","clinical_significance":[],"end":140624489,"alleles":["C","T"],"strand":1,"feature_type":"variation","start":140624489,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"clinical_significance":[],"id":"rs1419988422","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","A"],"end":140624490,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624490},{"clinical_significance":[],"seq_region_name":"7","id":"rs1563185172","consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624491,"feature_type":"variation","strand":1,"end":140624491,"alleles":["A","-"]},{"id":"rs1386670955","seq_region_name":"7","clinical_significance":[],"start":140624493,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140624493,"alleles":["G","C"],"strand":1,"feature_type":"variation"},{"seq_region_name":"7","id":"rs1800432810","clinical_significance":[],"alleles":["G","C"],"end":140624496,"strand":1,"feature_type":"variation","start":140624496,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant"},{"seq_region_name":"7","id":"rs1156374749","clinical_significance":[],"strand":1,"feature_type":"variation","alleles":["G","A"],"end":140624497,"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140624497,"source":"dbSNP"},{"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140624498,"source":"dbSNP","strand":1,"feature_type":"variation","end":140624498,"alleles":["T","G"],"seq_region_name":"7","id":"rs1800433158","clinical_significance":[]},{"seq_region_name":"7","id":"rs1800433317","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140624503,"source":"dbSNP","strand":1,"feature_type":"variation","end":140624503,"alleles":["G","A"]},{"end":140624505,"alleles":["T","A"],"feature_type":"variation","strand":1,"source":"dbSNP","start":140624505,"consequence_type":"intron_variant","assembly_name":"GRCh38","clinical_significance":[],"seq_region_name":"7","id":"rs1800433475"},{"clinical_significance":[],"seq_region_name":"7","id":"rs1585779683","feature_type":"variation","strand":1,"alleles":["A","C"],"end":140624507,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624507},{"id":"rs1469124261","seq_region_name":"7","clinical_significance":[],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140624513,"source":"dbSNP","strand":1,"feature_type":"variation","end":140624513,"alleles":["C","T"]},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624517,"feature_type":"variation","strand":1,"end":140624517,"alleles":["T","A"],"clinical_significance":[],"seq_region_name":"7","id":"rs1378149430"},{"start":140624525,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140624525,"alleles":["C","T"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1200851007","clinical_significance":[]},{"clinical_significance":[],"id":"rs796786037","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","A","T"],"end":140624528,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624528},{"seq_region_name":"7","id":"rs2130726712","clinical_significance":[],"start":140624532,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["G","A"],"end":140624532,"strand":1,"feature_type":"variation"},{"feature_type":"variation","strand":1,"end":140624541,"alleles":["G","A"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624541,"clinical_significance":[],"seq_region_name":"7","id":"rs1217049947"},{"start":140624542,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","end":140624542,"alleles":["T","G"],"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585779729","clinical_significance":[]},{"seq_region_name":"7","id":"rs918436567","clinical_significance":[],"strand":1,"feature_type":"variation","end":140624550,"alleles":["G","C"],"assembly_name":"GRCh38","consequence_type":"intron_variant","start":140624550,"source":"dbSNP"},{"clinical_significance":[],"id":"rs1800434943","seq_region_name":"7","feature_type":"variation","strand":1,"alleles":["C","G"],"end":140624553,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624553},{"start":140624555,"source":"dbSNP","assembly_name":"GRCh38","consequence_type":"intron_variant","alleles":["C","G"],"end":140624555,"strand":1,"feature_type":"variation","seq_region_name":"7","id":"rs1585779739","clinical_significance":[]},{"feature_type":"variation","strand":1,"alleles":["G","A"],"end":140624558,"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624558,"clinical_significance":[],"seq_region_name":"7","id":"rs77169094"},{"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624560,"feature_type":"variation","strand":1,"alleles":["C","G","T"],"end":140624560,"clinical_significance":[],"seq_region_name":"7","id":"rs1800435405"},{"clinical_significance":[],"seq_region_name":"7","id":"rs755707474","feature_type":"variation","strand":1,"end":140624564,"alleles":["CTCCT","CT"],"consequence_type":"intron_variant","assembly_name":"GRCh38","source":"dbSNP","start":140624560}]